The present invention relates to compounds that are useful as a plasminogen activator inhibitor-1 (hereinafter referred to as PAI-1) inhibitor and uses thereof.
It is known that an overexpression of plasminogen activator inhibitor-1 (PAI-1) inhibits the production of plasmin that decomposes fibrin thrombi and tissue proteins and brings a formation of thrombi (for example, refer to the Non-patent Document 2) by inhibiting the activation of plasminogen activator (for example, tissue-type plasminogen activator and urokinase-type plasminogen activator).
Furthermore, the overexpression of PAI-1 is observed in arteriosclerotic lesions, and is known to increase a risk of thrombotic diseases such as cardiac infarction, deep-vein thrombosis (DVT), disseminated intravascular coagulation (DIC) following sepsis and the like (refer to the Non-patent Document 1).
From these facts, compounds that inhibit PAI-1 activity or production are useful for the suppression of forming thrombus, and are expected to be useful drugs to diseases caused by the formation of thrombi such as thrombotic diseases, diseases involving thrombus formation and the like.
Furthermore, it is known that PAI-1 promotes precipitation and accumulation of extracellular matrix and is deeply involved in the development of tissue lesion featuring fibrosis and vascular wall sclerotic lesion. As an extracellular matrix accumulation in the airway of an asthma model mouse is reduced by a PAI-1 knockout (refer to the Non-patent Document 8), it is suggested that PAI-1 is directly involved in the fibrosis. Therefore, compounds that inhibit the activity or production of PAI-1 are useful for the inhibition of fibrosis of tissue, and are expected to be useful drugs to a diseases caused by the fibrosis of tissue.
Besides, PAI-1 is also secreted from mast cells (refer to the Non-patent Document 7), and it is reported that the blood level is high in an obesity model mouse, and is synthesized not only in the endothelial tissue and in the hepatic tissue, but also synthesized in the fatty tissue. Particularly in the visceral fat, PAI-1 synthesis amount is exponentially enhanced together with its deposition (refer to the Non-patent Document 3). Moreover, in the obesity model mouse where PAI-1 gene is knocked out, a decrease of weight and a lowering of blood glucose level and blood insulin level are reported (refer to the Non-patent Document 4), and it shows that PAI-1 has a possibility to aggravate various pathological conditions caused by the fat deposition. Therefore, compounds that inhibit the activity or the production of PAI-1 are useful for the inhibition of visceral fat deposition, and are expected to be useful drugs to diseases caused by the visceral fat deposition.
Furthermore, from the facts that PAI-1 inhibits an adhesion of cell and extracellular matrix by binding to a vitronectin which is a cell adhesion factor, a PAI-1 antibody inhibits a cancer metastasis in a cancer model (refer to the Non-patent Document 5), and the infiltration of cancer and an angiogenesis are inhibited when malignant keratinocytes are transplanted to the PAI-1 knockout mouse (refer to the Non-patent Document 6), compounds that inhibit the activity or the production of PAI-1 are useful for the inhibition of cell migration, cell metastasis, angiogenesis and the like, and are expected to have therapeutic effects to diseases caused by cell migration, cell metastasis, angiogenesis and the like.
Moreover, arterial lesions as an acute rejection and a chronic rejection after heart or kidney transplantation are considered to be caused by the development of tissue fibrosis, the formation of thrombi, and the proliferation and the remodeling of arterial endothelial cell. Since, in the heart transplantation experiment using mise (murine), when a compound having an inhibitory activity to PAI-1 is administered, a graft survival is significantly prolonged compared with the control group and the rate of serious intimal hypertrophy is reduced to one third (refer to the Patent Document 1), compounds that inhibit the activity or the production of PAI-1 are expected as a medicament to inhibit an acute rejection and an arterial lesion after transplantation, after heart or kidney transplantation or transplantation of other organs.
On the other hand, as plasmin which is activated by inhibiting PAI-1 is involved not only in the decomposition of thrombi, but also in the remodeling of tissue, the migration, metastasis and infiltration of cells, the ovulation and implantation, the activation of transforming growth factors which are cytostatic cytokines, and the activation of collagenase, compounds that inhibit the activity or the production of PAI-1 are useful for the inhibition of tissue remodeling, the proliferation, migration, infiltration, and metastasis of cells, angiogenesis and the like, and treatment effects are expected to diseases caused by cell proliferation, angiogenesis, and remodeling of tissues and the like.
In the past, examples of compounds having PAI-1 inhibition activity include, for example, the compounds disclosed in the Patent Documents 1 to 19 and the Non-patent Documents 9 to 11. On the other hand, some compounds have been reported (refer to the Patent Documents 20 to 22) as oxamic acid derivatives, however, it is not known whether they have PAI-1 inhibition activity.
[Non-patent Document 1] Proc. Natl. Acad. Sci. USA, Vol. 89, No. 15, pp. 6998-7002 (1992).
[Non-patent Document 3] Mol. Med., Vol. 2, No. 5, pp. 568-582 (1996).
[Non-patent Document 5] Gen. Diagn. Pathol., Vol. 141, No. 1, pp. 41-48 (1995).
[Non-patent Document 6] Nat. Med., Vol. 4, No. 8, pp. 923-928 (1998).
[Non-patent Document 8] Biochem. Biophys. Res. Commun., Vol. 294, No. 5, pp. 1155-1160 (2002).
[Non-patent Document 10] J. Med. Chem., Vol. 47, No. 14, pp. 3491-3494 (2004).
[Non-patent Document 11] Mukul R. Jain et al., Eur. J. Med. Chem., Vol. 43 (4), pp. 880-884 (2008), Epub Jun. 3 (2007). [PubMed ID: 17664030]
An object of the present invention is to provide compounds having an inhibitory activity on PAI-1 and uses thereof.
The inventors of the present invention conducted various studies to solve the aforementioned problems, and found as a result that the compounds represented by the following formula (I), the salts thereof and the like had inhibitory action on PAI-1, and achieved the present invention:
wherein:
R1 represents a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the following substituent group α-1, wherein, when the number of the substituents is two or more, each of the substituents may be the same or different;
T represents a single bond, a 1,4-piperazinylene, —R″—, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)—, the formula —N(R′)C(═O)— or the formula —SO2N(R′)—, wherein the bond at the left-hand end binds to R1, and the bond at the right-hand end binds to E in each of the formulas;
R′ represents a hydrogen atom or a C1-6 alkyl group;
m represents 0 or 1;
when m is 0, G represents the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H or the formula —(CH2)j—N—W′—CO2H, wherein the bond at the left-hand end binds to E, and the nitrogen atom binds to M in each of the formulas, wherein
j represents 0 or 1;
h represents 0, 1, 2 or 3;
when m is 1, G represents a single bond, an oxygen atom, —C(═O)— or a sulfur atom;
when m is 0, R2 represents a hydrogen atom, a C3-8 cycloalkyl group, a C1-6 alkyl substituted C3-8 cycloalkyl group, a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the following substituent group β-1, wherein, when the number of the substituents is two or more, each of the substituents may be the same or different;
when m is 1, R2 represents a hydrogen atom, a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the following substituent group β-1, wherein, when the number of the substituents is two or more, each of the substituents may be the same or different;
E represents the following formula (II):
wherein
when m is 1, R34 or R35 represents the formula —X—Y′, wherein
when R35 represents the formula —X—Y′, one of R31, R32, R33 and R34 represents the formula R1-T-, and each of the other three independently represents a hydrogen atom or a group selected from the following substituent group γ-1;
when R34 represents the formula —X—Y′, one of R31, R32 and R33 represents the formula R1-T-, each of the other two independently represents a hydrogen atom or a group selected from the following substituent group γ-1, and R35 represents the a hydrogen atom;
when m is 0, one of R31, R32, R33 and R34 represents the formula R1-T-, each of the other three independently represents a hydrogen atom or a group selected from the following substituent group γ-1, and R35 represents a hydrogen atom or a group selected from the following substituent group γ-1;
X represents a single bond, —CH═CH—, —C(═O)—, the formula —V′—(V′)k—, the formula —N(R4)—C(═O)—, the formula —N(R4)—V′— or the formula —(V′)k—R″—W′—, wherein the bond at the left-hand end binds to the benzene ring E and the bond at the right-hand end binds to Y′ in each of the formulas;
R4 represents a hydrogen atom or a C1-6 alkyl group;
R″ represents an oxygen atom or a sulfur atom;
V′ represents a methylene group or a methylene group substituted with one or two groups selected from the following substituent group δ-1;
W′ represents the formula -J1-J2-J3-, wherein, when G is the formula —(CH2)j—N—W′—CO2H, J1 binds to the nitrogen atom and J3 binds to the carboxy group; and when X is the formula —(V′)k—R″—W′—, J1 binds to R″ and J3 binds to Y′;
J1 represents a methylene group or a methylene group substituted with one or two groups selected from the following substituent group ε-1 wherein, when the number of the substituents is two, each of the substituents may be the same or different;
each of J2 and J3 independently represents a single bond, a methylene group or a methylene group substituted with one or two groups selected from the following substituent group ε-1, wherein, when the number of the substituents is two, each of the substituents may be the same or different;
k represents 0, 1 or 2;
Y′ represents a carboxy group or a 1H-tetrazol-5-yl group;
M represents a single bond, the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r- wherein, the bond at the left-hand end binds to G, and the bond at the right-hand end binds to R2 in each of the formulas);
each of Q1, Q2 and Q3 independently represents a methylene group or a methylene group substituted with one or two groups selected from the following substituent group ζ-1, wherein, when the number of the substituents is two, each of the substituents may be the same or different;
U′ represents an oxygen atom, or a sulfur atom;
n represents an integer of 1 to 10;
p represents an integer of 0 to 10;
q represents 0 or 1;
r represents an integer of 0 to 10;
when M is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the sum of n, p and r is an integer of 1 to 10;
when M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, the sum of n, p, q and r is an integer of 1 to 10,
a halogen atom, a cyano group, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group, a C1-6 alkylenedioxy group, a C1-6 alkylsulfonyl group, a C1-6 alkylcarbonyl group, a C1-6 alkylsulfonylamino group, a hydroxy group and a carboxy substituted C1-6 alkyl group;
a halogen atom, a nitro group, a hydroxy group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a phenyl group, a carboxy group, a carboxy substituted C1-6 alkyl group, a halogenated C1-6 alkoxy substituted phenyl group, a carboxy substituted C1-6 alkoxy group, a C1-6 alkyl substituted phenyl group and a carboxy substituted C2-6 alkenyl group;
a halogen atom, a C1-10 alkyl group, a carboxy substituted C1-10 alkyl group, a halogenated C1-10 alkyl group, a C1-20 alkoxy group, a C3-8 cycloalkoxy group, a C3-8 cycloalkoxy group substituted with one or two C1-6 alkyl groups, a halogenated C1-20 alkoxy group, a carboxy substituted C1-20 alkoxy group, a hydroxy group, a hydroxy substituted C1-20 alkoxy group, a C1-6 alkoxy substituted C1-10 alkoxy group, a C3-8 cycloalkyl substituted C1-20 alkoxy group, a phenyl substituted C1-20 alkoxy group wherein the phenyl group may be substituted with one to five groups selected from the following substituent group η-1, a phenoxy group wherein the phenyl group may be substituted with one to five groups selected from the following substituent group η-1, a phenoxy substituted C1-20 alkoxy group, a di(C1-10 alkyl)amino group, an adamantyloxy group, a 5 to 7-membered completely saturated heterocyclic group (the heterocyclic group comprises one nitrogen atom as the ring-constituting atom and may further comprise one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom as the ring-constituting atom, and the heterocyclic group binds to E via the nitrogen atom that is the ring-constituting atom), and a 5 to 7-membered completely saturated heterocyclic group substituted with one group selected from the following substituent group θ-1 (the heterocyclic group comprises one nitrogen atom as the ring-constituting atom and may further comprise one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom as the ring-constituting atom, and the heterocyclic group binds to E via the nitrogen atom that is the ring-constituting atom);
a C1-6 alkyl group;
a halogen atom and a C1-10 alkyl group;
a C1-6 alkyl group, a phenyl group and a carboxy group;
a C1-6 alkyl group and a halogenated C1-6 alkoxy group;
an oxo group.
The present invention thus provides:
[1] a compound represented by the aforementioned formula (I), a salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt, provided that:
when G is the formula N—C(═O)—CO2H, E is the following formula:
R1 is a phenyl group substituted with one halogenated C1-6 alkoxy group, T is a single bond, R2 is a phenyl group or a phenyl group substituted with one or two halogenated C1-6 alkyl groups, M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, n is 1, p is 0, q is 0, and r is 0, Q1 is a methylene group substituted with one or two groups selected from the substituent group ζ-1, wherein, when the number of the substituents is two, each of the substituents may be the same or different;
when G is the formula N—C(═O)—CO2H, E is the following formula:
R1 is a phenyl group substituted with one or two substituents selected from a halogen atom, a halogenated C1-6 alkyl group, a C1-6 alkoxy group and a halogenated C1-6 alkoxy group wherein, when the number of the substituents is two, each of the substituents may be the same or different, and R2 is a phenyl group substituted with two halogenated C1-6 alkyl groups, T is a single bond, a 1,4-piperazinylene, —R″—, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)— or the formula —N(R′)C(═O)—;
when G is the formula N—C(═O)—CO2H, E is a benzene ring, R1 is a phenyl group, T is a single bond, and R2 is a 2-carboxyphenyl group, M is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-;
[2] a compound represented by the aforementioned formula (I), a salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt, provided that:
when G is the formula N—C(═O)—CO2H, E is the following formula:
R1 is a phenyl group substituted with one or two substituents selected from a halogen atom, a halogenated C1-6 alkyl group, a C1-6 alkoxy group and a halogenated C1-6 alkoxy group, wherein, when the number of the substituents is two, each of the substituents may be the same or different, and R2 is a phenyl group substituted with two halogenated C1-6 alkyl groups, T is a single bond, a 1,4-piperazinylene, —R″—, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)— or the formula —N(R′)C(═O)—;
when m is 0, G is the formula N—C(═O)—CO2H, E is a benzene ring, R1 is a phenyl group, T is a single bond, and R2 is a 2-carboxyphenyl group, M is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-;
when m is 0, one of R31, R32, R33 and R34 is the formula R1-T-, each of the other three is independently a hydrogen atom, a halogen atom, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a carboxy substituted C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl substituted C1-20 alkoxy group, wherein the phenyl group may be substituted with one to five groups selected from the following substituent group η-1 or a di(C1-6 alkyl)amino group, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a cyano group, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group and a C1-6 alkylsulfanyl group, G is the formula N—C(═O)—CO2H, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a hydroxy group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group and a phenyl group, and T is a single bond or an oxygen atom, M is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, provided that when M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, n is 1, p is 0, q is 0, and r is 0, Q1 is a methylene group substituted with one or two groups selected from the substituent group ζ-1 (when the number of the substituents of the methylene group is two, each of the substituents may be the same or different);
when m is 1, R33 is the formula R1-T-, R31, R32 and R34 is a hydrogen atom, R35 is the formula —X—Y′, T is a single bond, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group and a C1-6 alkylenedioxy group, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl group, a C1-6 alkylsulfanyl group and a phenyl group, G is an oxygen atom, and M is a single bond or —CH2—, X is a single bond, —C(═O)—, the formula —V′—(V′)k—, the formula —N(R4)—V′— or the formula —(V′)k—R″—W′—, provided that when X is —V′—, V′ is a methylene group substituted with one or two groups selected from the following substituent group δ-1, and when X is —V′—V′—, one of V′ or each of V′ is a methylene group substituted with one or two groups selected from the following substituent group δ-1;
when m is 1, R35 is the formula —X—Y′, X is —CH2—, —CH2CH2—, —CH═CH— or —N(R4)—C(═O)—, T is a single bond, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group and a C1-6 alkylenedioxy group, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl group and a carboxy group, G is an oxygen atom, and M is a single bond or —CH2—, one of R31, R32 and R34 is the formula R1-T-;
when m is 1, X is —CH2—, —CH2CH2—, —CH═CH— or —N(R4)—C(═O)—, R33 is the formula R1-T-, R31, R32 and R34 are hydrogen atoms, R35 is the formula —X—Y′, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group and a C1-6 alkylenedioxy group, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl group and a carboxy group, G is an oxygen atom, and M is a single bond or —CH2—, T is a 1,4-piperazinylene, —R″—, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)—, the formula —N(R′)C(═O)— or the formula —SO2N(R′)—;
when m is 1, X is —CH2—, —CH2CH2—, —CH═CH— or —N(R4)—C(═O)—, R33 is the formula R1-T-, R35 is the formula —X—Y′, T is a single bond, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group and a C1-6 alkylenedioxy group, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl group and a carboxy group, G is an oxygen atom, and M is a single bond or —CH2—, at least one of R31, R32 and R34 is a group selected from the substituent group γ-1; and
when m is 1, X is —CH2—, —CH2CH2—, —CH═CH— or —N(R4)—C(═O)—, R33 is the formula R1-T-, R31, R32 and R34 are hydrogen atoms, R35 is the formula —X—Y′, T is a single bond, R1 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group and a C1-6 alkylenedioxy group, R2 is a C6-10 aryl group or a C6-10 aryl group substituted with a group or groups selected from a halogen atom, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a phenyl group and a carboxy group, and G is an oxygen atom, M is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, provided that when M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, n is 1, p is 0, q is 0, and r is 0, Q1 is a methylene group substituted with one or two groups selected from the substituent group ζ-1,
[3] the compound, the salt thereof, the hydrate of the compound, the hydrate of the salt, the solvate of the compound or the solvate of the salt according to the aforementioned [1] or [2], wherein m is 0;
[4] the compound, the salt thereof, the hydrate of the compound, the hydrate of the salt, the solvate of the compound or the solvate of the salt according to the aforementioned [1] or [2], wherein m is 1, provided that:
when X is the formula —N(R4)—C(═O)— or the formula —N(R4)—V′—, R2 is a hydrogen atom, M is a single bond, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, and U′ is an oxygen atom, or
when X is the formula —N(R4)—C(═O)— or the formula —N(R4)—V′—, R2 is a phenyl group or a phenyl group substituted with one to five substituents selected from the following substituent group η-1, M is a single bond, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, and q is 0, or
when X is the formula —N(R4)—C(═O)— or the formula —N(R4)—V′—, R2 is a phenyl group, M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, U′ is an oxygen atom, and q is 1,
G is a single bond, —C(═O)— or a sulfur atom;
[5] a pharmaceutical composition comprising, as an active ingredient, the compound according to any on of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt;
[6] a method of inhibiting PAI-1, comprising the step of allowing the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt to act on PAI-1;
[7] a method of inhibiting PAI-1 in a mammal, comprising the step of administering the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt at a dose sufficient to inhibit PAI-1;
[8] a method for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity in a mammal, comprising the step of administering the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt at a dose sufficient to prevent and/or treat the disease;
[9] A PAI-1 inhibitor comprising, as an active ingredient, the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt;
[10] a medicament for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity, comprising, as an active ingredient, the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt;
[11] use of the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt, for the manufacture of a PAI-1 inhibitor;
[12] use of the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt, for the manufacture of a medicament for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity;
[13] the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the salt, a solvate of the compound or a solvate of the salt, for inhibiting PAI-1; and
[14] the compound according to any one of the aforementioned [1] to [4], a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound or a solvate of the salt, for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity.
In the present specification, the wording “allow (something) to act” means “allow (something) to exert an inhibitory function on PAI-1 activation” by adding or administering the compound represented by the formula (I), a pharmacologically acceptable salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the aforementioned compound, or a solvate of the aforementioned salt. The object to be targeted for the function may be PAI-1, or cultured cells or cells in an individual organism which produce PAI-1. The aforementioned individual organism may be a human or another mammal.
The compounds of the present invention have an inhibitory activity on PAI-1. Therefore, the compounds of the present invention are useful as a medicament for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity.
Embodiments of the present invention accomplished based on the above-described findings are hereinafter described in detail by giving Examples. When using commercial reagent kits and measuring apparatus, unless otherwise explained, attached protocols to them are used. The objective, characteristics, and advantages of the present invention as well as the idea thereof will be apparent to those skilled in the art from the descriptions given herein. It is to be understood that the embodiments and specific examples of the invention described hereinbelow are to be taken as preferred examples of the present invention. These descriptions are for illustrative and explanatory purposes only and are not intended to limit the invention to these embodiments or examples. It is further apparent to those skilled in the art that various changes and modifications may be made based on the descriptions given herein within the intent and scope of the present invention disclosed herein.
The abbreviations used in the following tables have the following meanings. Me: methyl group, Et: ethyl group, n-Pr: n-propyl group, i-Pr: isopropyl group, n-Bu: n-butyl group, t-Bu: tert-butyl group, n-Pen: n-pentyl group, n-Hex: n-hexyl group, n-Hep: n-heptyl group, n-Oct: n-octyl group, n-Non: n-nonyl group, n-Dec: n-decyl group, Ph: phenyl group, OMe: methoxy group, n-PrO: n-propoxy group, i-PrO: isopropoxy group, n-BuO: n-butoxy group, t-BuO: tert-butoxy group, SMe: methylsulfanyl group, Bn: benzyl group.
In the present invention, R1 in the aforementioned formula (I) represents a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the aforementioned substituent group α-1 (when the number of the substituents is two or more, each of the substituents may be the same or different).
R1 is preferably the following formula (III):
wherein each of R11, R12, R13, R14 and R15 independently represents a hydrogen atom or a group selected from the following substituent group α-2, or R11 and R12, R12 and R13, R13 and R14, or R14 and R15 are taken together to form a ring-constituting C1-6 alkylenedioxy group;
a halogen atom, a cyano group, a nitro group, a C1-6 alkyl group, a halogenated C1-6 alkyl group, a C1-6 alkoxy group, a halogenated C1-6 alkoxy group, a C1-6 alkylsulfanyl group, a carboxy group, an amino group, a C1-6 alkylsulfonyl group, a C1-6 alkylcarbonyl group, a C1-6 alkylsulfonylamino group, a hydroxy group and a carboxy substituted C1-6 alkyl group.
Each of R11, R12, R13, R14 and R15 is preferably and independently a hydrogen atom or a group selected from the following substituent group α-3, or R11 and R12, R12 and R13, R13 and R14, or R14 and R15 are taken together to form preferably a ring-constituting methylenedioxy group;
a halogen atom, a cyano group, a nitro group, a methyl group, an isopropyl group, a n-butyl group, a tert-butyl group, a trifluoromethyl group, a methoxy group, an isopropyloxy group, a n-butykoxy group, a tert-butyloxy group, a n-pentyloxy group, a 1-ethylpropoxy group, a trifluoromethoxy group, a methylsulfanyl group, a carboxy group, an amino group, a methysulfonyl group, an acetyl group, a methylsulfonylamino group and a hydroxy group.
R11, R12, R13, R14 and R15 are preferably any one of the followings:
(1) all of R11, R12, R13, R14 and R15 is are hydrogen atoms; (2) four of R11, R12, R13, R14 and R15 are hydrogen atoms and the other one is a group selected from the substituent group α-3; (3) three of R11, R12, R13, R14 and R15 are hydrogen atoms and the other two are groups selected from the substituent groups α-2 or α-3; or (4) among R11, R12, R13, R14 and R15, R11 and R12, R12 and R13, R13 and R14, or R14 and R15 are taken together to form a ring-constituting methylenedioxy group, and all the others are hydrogen atoms.
R1 is preferably a group selected from the following substituent group α-4.
T in the aforementioned formula (I) represents a single bond, a 1,4-piperazinylene, —O—, —S—, —N(R′)—, the formula —CH2O —, the formula —CH2S —, the formula —C(═O)N(R′)—, the formula —N(R′)C(═O)— or the formula —SO2N(R′)— (in each of the formulas, the bond at the left-hand end binds to R1, and the bond at the right-hand end binds to E). R′ represents a hydrogen atom or a C1-6 alkyl group. Examples of the aforementioned —N(R′)— include —N(H)—, —N(Me)- and the like. Examples of the aforementioned formula —C(═O)N(R′)— include —C(═O)N(H)—, —C(═O)N(Me)- and the like. Examples of the aforementioned formula —N(R′)C(═O)— include —N(H)C(═O)—, —N(Me)C(═O)— and the like. Examples of the aforementioned formula —SO2N(R′)—include —SO2N(H)— and the like. m in the aforementioned formula (I) represents 0 or 1. When m is 0, then G in the aforementioned formula (I) represents the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H or the formula —(CH2)j—N—W′—CO2H (in each of the formulas, the bond at the left-hand end binds to E, and the nitrogen atom binds to M). j represents 0 or 1. h represents 0, 1, 2 or 3. Examples of the aforementioned formula —(CH2)j—N—C(═O)—(CH2)h—CO2H include —N—C(═O)—CO2H, —CH2—N—C(═O)—CO2H, —N—C(═O)—CH2—CO2H, —N—C(═O)—(CH2)2—CO2H, —N—C(═O)—(CH2)3—CO2H and the like. Examples of the aforementioned formula —(CH2)j—N—W′—CO2H include —N—CH2—CO2H, —N—(CH2)2—CO2H, —N—CH(n-Bu)-CO2H, —CH2—N—CH2—CO2H and the like. When m is 1, then G in the aforementioned formula (I) represents a single bond, an oxygen atom, —C(═O)— or a sulfur atom.
R2 in the aforementioned formula (I) represents a hydrogen atom, a C3-8 cycloalkyl group, a C1-6 alkyl substituted C3-8 cycloalkyl group, a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the aforementioned substituent group β-1 (when the number of the substituents is two or more, each of the substituents may be the same or different).
When R2 is a C3-8 cycloalkyl group or a C1-6 alkyl substituted C3-8 cycloalkyl group, examples of R2 include any one of the following substituent groups.
When R2 is a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the substituent group β-1 (when the number of the substituents group is two or more, each of the substituents may be the same or different), R2 is preferably the following formula (IV):
wherein each of R21, R22, R23, R24 and R25 independently represents a hydrogen atom or a group selected from the substituent group β-1.
Each of R21, R22, R23, R24 and R25 is preferably and independently a hydrogen atom or a group selected from the following substituent group β-2;
a halogen atom, a nitro group, a hydroxy group, a methyl group, a-isopropyl group, a n-butyl group, a tert-butyl group, a 1,1-dimethylpropyl group, a trifluoromethyl group, a methoxy group, a n-butyloxy group, a tert-butyloxy group, a trifluoromethoxy group, a methylsulfanyl group, a phenyl group, a carboxy group, a 2-carboxyethyl group, —CH═CH—COOH, —OCH2COOH, a benzyloxy group, a 4-tert-butyl-phenyl group and a 4-trifluoromethoxy-phenyl group.
R21, R22, R23, R24 and R25, are preferably any one of the followings:
(1) all of R21, R22, R23, R24 and R25 are hydrogen atoms; (2) four of R21, R22, R23, R24 and R25 are hydrogen atoms and the other one is a group selected from the substituent group β-3; or (3) three of R21, R22, R23, R24 and R25 are hydrogen atoms and each of the other two is independently a group selected from the substituent groups β-1 or β-2.
When R2 is a C6-10 aryl group or a C6-10 aryl group substituted with one to five groups selected from the substituent group β-1 (when the number of the substituents is two or more, each of the substituents may be the same or different), R2 is preferably a group selected from the following substituent group β-3.
E in the aforementioned formula (I) represents the following formula (II):
wherein:
when m is 1, R34 or R35 represents the formula —X—Y′, wherein
when R35 represents the formula —X—Y′, one of R31, R32, R33, and R34 represents the formula R1-T-, and each of the other three independently represents a hydrogen atom, or a group selected from the aforementioned substituent group γ-1,
when R34 represents the formula —X—Y′, one of R31, R32, and R33 represents the formula R1-T-, each of the other two independently represents a hydrogen atom or a group selected from the substituent group γ-1, and R35 represents a hydrogen atom,
when m is 0, one of R31, R32, R33, and R34 represents the formula R1-T-, each of the other three independently represents a hydrogen atom or a group selected from the substituent group γ-1, and R35 represents a hydrogen atom or a group selected from the substituent group γ-1.
In the aforementioned substituent group γ-1, examples of the C3-8 cycloalkoxy group or the C3-8 cycloalkoxy group substituted with one or two C1-6 alkyl groups selected from the substituent group β-1 include any one of the following substituent groups.
In the aforementioned substituent group γ-1, examples of the C3-8 cycloalkyl substituted C1-20 alkoxy group include a cyclopentyl substituted C1-20 alkoxy group or a cyclohexyl substituted C1-20 alkoxy group. In the aforementioned substituent group γ-1, the phenyl group of the phenyl substituted C1-20 alkoxy group or of the phenoxy group may optionally be substituted with one to five substituents (when the number of the substituents is two or more, each of the substituents may be the same or different). The substituent is preferably a group selected from the substituent group η-1. The substituent is more preferably a methyl group, a tert-butyl group or a trifluoromethoxy group. In the aforementioned substituent group γ-1, the phenoxy group of the phenoxy substituted C1-20 alkoxy group may optionally be substituted with one to five substituents (when the number of the substituents is two or more, each of the substituents may be the same or different). Examples of the substituent include a group selected from the substituent group η-1.
In the aforementioned substituent group γ-1, the 5 to 7-membered completely saturated heterocyclic group (the heterocyclic group comprises one nitrogen atom as the ring-constituting atom and may further comprise one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom as the ring-constituting atom, and the heterocyclic group binds to E via the nitrogen atom that is the ring-constituting atom) is preferably a pyrrolidin-1-yl group, a hexahydro-1H-azepin-1-yl group, a thiomorpholin-1-yl group, a piperidin-1-yl group and a morpholin-4-yl group. The aforementioned 5 to 7-membered completely saturated heterocyclic group may optionally be substituted with one or two substituents (when the number of the substituents is two or more, each of the substituents may be the same or different). Examples of the aforementioned 5 to 7-membered completely saturated heterocyclic group which is substituted include a 2-piperidon-1-yl group.
When R31, R32, R33; R34 or R35 is not the formula —X—Y′ and the formula R1-T-, R31, R32, R33, R34 or R35 are preferably a hydrogen atom, or a group selected from the following substituent group γ-2;
a halogen atom, a methyl group, a n-heptyl group, a 2-carboxyethyl group, a trifluoromethyl group, a methoxy group, a n-propoxy group, an isopropoxy group, a n-butoxy group, a tert-butoxy group, a n-pentyloxy group, a 1-ethylpropoxy group, a n-hexyloxy group, a n-heptyloxy group, a n-octyloxy group, a 2-tert-butoxy-ethoxy group, a n-nonyloxy group, a n-decyloxy group, a n-pentadecyloxy group, a trifluoromethoxy group, —O(CH2)2CF3, —O(CH2)4CF3, a benzyloxy group, a 4-(tert-butyl)benzyloxy group, a dimethylamino group, a diethylamino group, a piperidin-1-yl group, a 2-oxopiperidin-1-yl group, a morpholin-4-yl group, a pyrrolidin-1-yl group, a azepan-1-yl group, a thiomorpholin-4-yl group, a hydroxy group, —O(CH2)6COOH, —O(CH2)8COOH, a 2-adamantyloxy group, —O(CH2)5—OH, a 4-(tert-butyl)phenoxy group, a phenoxy group, a 3,5-dimethylbenzyloxy group, —O(CH2)4-Ph, a 4-trifluoromethoxybenzyloxy group, —O(CH2)3—O-Ph, a 3-cyclopentylpropoxy group, a 3-cyclohexylpropoxy group, a cyclohexyoxy group, a 4-(n-butyl)cyclohexyoxy group, a 2-isopropyl-5-methyl-cyclohexyloxy group, a cyclopentyloxy group and a cycloheptyloxy group.
When m is 1, it is preferable that two or three of R31, R32, R33 and R34 are hydrogen atoms. When m is 0, it is preferable that two to four of R31, R32, R33, R34 and R35 are hydrogen atoms.
X in the aforementioned formula (I) represents a single bond, —CH═CH—, —C(═O)—, the formula —V′—(V′)k—, the formula —N(R4)—C(═O)—, the formula —N(R4)—V′— or the formula —(V′)k—R″—W′— (in each of the formulas, the bond at the left-hand end binds to the benzene ring E, and the bond at the right-hand end binds to Y′). The aforementioned R4 represents a hydrogen atom or a C1-6 alkyl group. R4 is preferably a hydrogen atom or a methyl group. The aforementioned R″ represents an oxygen atom or a sulfur atom. The aforementioned V′ represents a methylene group or a methylene group substituted with one or two C1-6 alkyl groups (when the methylene group is substituted with two C1-6 alkyl groups, each of the C1-6 alkyl groups may be the same or different). The aforementioned W′ represents the formula -J1-J2-J3- (in the formula, when G is the formula —(CH2)j—N—W′—CO2H, then J1 binds to the nitrogen atom, and J3 binds to the carboxy group; when X is the formula —(V′)k—R″—W′—, J1 binds to R″, and J3 binds to Y′). The aforementioned J1 represents a methylene group or a methylene group substituted with one or two groups selected from the aforementioned substituent group ε-1 (when the number of the substituents is two, each of the substituents may be the same or different). Each of the aforementioned J2 and J3 independently represents a single bond, a methylene group or a methylene group substituted with one or two groups selected from the substituent group ε-1 (when the number of the substituent is two, each of the substituents may be the same or different).
The aforementioned W′ is preferably a C1-3 straight chain alkylene group or a C1-3 straight chain alkylene group wherein a part or all of the hydrogen atoms are substituted with a group or groups selected from the substituent group ε-1 (when the number of the substituents is two or more, each of the substituents may be the same or different). The aforementioned k represents 0, 1 or 2.
Examples of the aforementioned formula —V′—(V′)k— include —CH2—, —(CH2)2—, —(CH2)3—, —CH(n-Bu)-CH2— and the like. Examples of the aforementioned formula —N(R4)—C(═O)— include —N(H)—C(═O)—, —N(Me)-C(═O)— and the like. Examples of the aforementioned formula —N(R4)—V′— include —N(H)—C(Me)2-, —N(H)—CH(n-Bu)-, —N(n-Bu)-CH2—, —N(n-Pr)-CH2—, —N(H)—CH2—, —N(Me)-CH2— and the like. Examples of the aforementioned formula —(V′)k—R″—W′— include —OCH2—, —OC(Me)2-, —CH2—O—CH2—, —CH(Me)-O—CH2—, —O(CH2)3—, —CH2—O—C(Me)2-, —OCH(Et)-, —OCHF—, —OCF2—, —OCH(n-Bu)-, —OCH(n-Hex)-, —O(CH2)2—CH(Me)- and the like.
Y′ in the aforementioned formula (I) represents a carboxy group or a 1H-tetrazol-5-yl group. M in the aforementioned formula (I) represents a single bond, the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r-, or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r- (in each of the formulas, the bond at the left-hand end binds to G, and the bond at the right-hand end binds to R2). Each of the aforementioned Q1, Q2 and Q3 independently represents a methylene group or a methylene group substituted with one or two groups selected from the aforementioned substituent group ζ-1 (when the number of the substituents is two, each of the substituents may be the same or different). Each of Q1, Q2 and Q3 is preferably and independently a methylene group or a group selected from the aforementioned substituent group ζ-2.
U′ represents an oxygen atom or a sulfur atom, n represents an integer of 1 to 10. p represents an integer of 0 to 10. q represents 0 or 1. r represents an integer of 0 to 10. When m is the formula —C(═O)-(Q1)n-(Q2)p-(Q3)r-, then the sum of n, p and r is an integer of 1 to 10. When m is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, then the sum of n, p, q and r is an integer of 1 to 10. M in the aforementioned formula (I) is preferably a single bond, the formula —C(═O)-Z1-, the formula -Z1-, the formula -Z2-O—, the formula -Z2-S— or the formula -Z3-O—CH2— (in each of the formulas, the bond at the left-hand end binds to G, and the bond at the right-hand end binds to R2). Z1 represents a C1-10 straight chain alkylene group or a C1-10 straight chain alkylene group wherein a part or all of the hydrogen atoms are substituted with groups selected from the substituent group ζ-1 (when the number of the substituents is two or more, each of the substituents may be the same or different). Z2 represents a C1-9 straight chain alkylene group or a C1-9 straight chain alkylene group wherein a part or all of the hydrogen atoms are substituted with groups selected from the substituent group ζ-1 (when the number of the substituents is two or more, each of the substituents may be the same or different). Z3 represents a C1-8 straight chain alkylene group or a C1-9 straight chain alkylene group wherein a part or all of the hydrogen atoms are substituted with groups selected from the substituent group ζ-1 (when the number of the substituents is two or more, each of the substituents may be the same or different). Each of Z1, Z2 and Z3 is preferably and independently a group selected from the following substituent group τ;
a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group and a pentane-1,5-diyl group.
M is preferably a single bond, —C(═O)—(CH2)3—, —CH2—, —(CH2)2—, —(CH2)3—, —(CH2)4—, —(CH2)5—, —(CH2)6—, —(CH2)7—, —(CH2)10—, —(CH2)3O—, —(CH2)4O—, —(CH2)5O—, —(CH2)3S—, —(CH2)3OCH2—, —CH(Me)-, —CH(n-Bu)-, —CH(Ph)- or —CH2—C(Me)2-CH2—.
Examples of the “halogen atom” in the aforementioned substituent groups α-1, β-1, γ-1 and ε-1 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
In the present specification, the “alkyl group” or an alkyl moiety of the substituents containing the alkyl moiety may be straight chain, branched chain or any combination of these. Examples of the “C1-6 alkyl group” in the aforementioned R′, R4 and substituent groups α-1, β-1, δ-1, ζ-1 and η-1 include a n-pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a 1-ethylpropyl group, a n-hexyl group and the like, besides C1-4 alkyl groups such as a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group and the like. Examples of the “C1-10 alkyl group” in the aforementioned substituent groups γ-1 and ε-1 include a n-heptyl group, a n-octyl group, a n-nonyl group, a n-decyl group and the like, besides the aforementioned C1-6 alkyl groups. Examples of the “C1-20 alkyl group” in the present specification include a n-undecyl group, a n-dodecyl group, a n-tridecyl group, a n-tetradecyl group, a n-pentadecyl group, a n-hexadecyl group, a n-heptadecyl group, a n-octadecyl group, a n-nonadecyl group, a n-icosyl group and the like, besides the aforementioned C1-10 alkyl groups.
Examples of the “C3-8 cycloalkyl group” in the aforementioned R2 include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group and a cyclooctyl group. The “C1-6 alkyl substituted C3-8 cycloalkyl group” means a group in which one or more hydrogen atoms in the C3-8 cycloalkyl group are substituted with C1-6 alkyl groups. Examples of the “C1-6 alkyl substituted C3-8 cycloalkyl group” include a 2-methylcyclopropyl group, a 1-methylcyclobutyl group, a 3-cyclopentyl group, a 4-methylcyclohexyl group, a 4-(tert-butyl)cyclohexyl group, a 3,5-dimethylcyclohexyl group, a 4,4-dimethylcyclohexyl group, a 4-methylcycloheptyl group, a 5-methylcyclooctyl group and the like.
The “halogenated C1-6 alkyl group” in the aforementioned substituent groups α-1 and β-1 means a group in which one or more hydrogen atoms in the C1-6 alkyl group are substituted with halogen atoms. Examples of the halogenated C1-6 alkyl group include a chloromethyl group, a bromomethyl group, a fluoromethyl group, a dichloromethyl group, a dibromomethyl group, a difluoromethyl group, a trichloromethyl group, a tribromomethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a nonafluorobutyl group, a perfluoropentyl group, a perfluorohexyl group and the like. The halogen atom of the halogenated C1-6 alkyl group is preferably a fluorine atom.
The “halogenated C1-10 alkyl group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms in the C1-10 alkyl group are substituted with halogen atoms. Examples of the halogenated C1-10 alkyl group include a perfluoroheptyl group, a perfluorooctyl group, a perfluorononyl group, a perfluorodecyl group and the like, besides the aforementioned halogenated C1-6 alkyl groups. The halogen atom of the halogenated C1-10 alkyl group is preferably a fluorine atom.
Examples of the C1-6 alkoxy group in the aforementioned substituent groups α-1 and β-1 include a methoxy group, an ethoxy group, a n-propoxy group, an isopropoxy group, a n-butoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxy group, a n-pentyloxy group, an isopentyloxy group, a neopentyloxy group, a tert-pentyloxy group, a 1-ethylpropoxy group, a n-hexyloxy group and the like.
Examples of the C1-20 alkoxy group in the aforementioned substituent group γ-1 include a n-heptyloxy group, a n-octyloxy group, a n-nonyloxy group, a n-decyloxy group, a n-undecyloxy group, a n-dodecyloxy group, a n-tridecyloxy group, a n-tetradecyloxy group, a n-pentadecyloxy group, a n-hexadecyloxy group, a n-heptadecyloxy group, a n-octadecyloxy group, a n-nonadecyloxy group, a n-icosyloxy group and the like, besides the aforementioned C1-6 alkoxy groups.
The “C3-8 cycloalkoxy group” in the aforementioned substituent group γ-1 means a group in which the hydrogen atom in the hydroxy group is substituted with a C3-8 cycloalkyl group. Examples of the C3-8 cycloalkoxy group include a cyclopropoxy group, a cyclobutoxy group, a cyclopentyloxy group, a cyclohexyloxy group, a cycloheptyloxy group and a cyclooctyloxy group. The “C3-8 cycloalkoxy group substituted with one or two C1-6 alkyl groups” in the aforementioned substituent group γ-1 means a group in which one or two hydrogen atoms in the C3-8 cycloalkoxy group are substituted with C1-6 alkyl groups. When two hydrogen atoms are substituted with C1-6 alkyl groups, each of the C1-6 alkyl groups may be the same or different. Examples of the C3-8 cycloalkoxy group substituted with one or two C1-6 alkyl group include a 2-methylcyclopropoxy group, a 1-methylcyclobutoxy group, a 3-cyclopentyloxy group, a 4-methylcyclohexyloxy group, a 4-(n-butyl)cyclohexyloxy group, a 2-isopropyl-5-methyl-cyclohexyloxy group, a 3,5-dimethylcyclohexyloxy group, a 4,4-dimethylcyclohexyloxy group, a 4-methylcycloheptyloxy group, a 5-methylcyclooctyloxy group and the like.
Examples of the halogenated C1-10 alkoxy group in the aforementioned substituent groups α-1, β-1 and η-1 include a chloromethoxy group, a bromomethoxy group, a fluoromethoxy group, a dichloromethoxy group, a dibromomethoxy group, a difluoromethoxy group, a trichloromethoxy group, a tribromomethoxy group, a trifluoromethoxy group, a 2,2,2-trifluoroethoxy group, a pentafluoroethoxy group, a heptafluoropropoxy group, a nonafluorobutoxy group, a perfluoropentyloxy group, a perfluorohexyloxy group and the like. Examples of the halogenated C1-20 alkoxy group in the aforementioned substituent group γ-1 include a perfluoroheptyloxy group, a perfluorooctyloxy group, a perfluorononyloxy group, a perfluorodecyloxy group, a perfluoroundecyloxy group, a perfluorododecyloxy group, a perfluorotridecyloxy group, a perfluorotetradecyloxy group, a perfluoropentadecyloxy group, a perfluorohexadecyloxy group, a perfluoroheptadecyloxy group, a perfluorooctadecyloxy group, a perfluorononadecyloxy group, a perfluoroicosyloxy group and the like, besides the aforementioned halogenated C1-6 alkoxy groups. Each of the halogen atoms of the halogenated C1-10 alkoxy group and the halogenated C1-20 alkoxy group is preferably a fluorine atom.
The “carboxy substituted C1-6 alkoxy group” in the aforementioned substituent group β-1 means a group in which one or more hydrogen atoms in the C1-6 alkoxy group are substituted with carboxy groups. Examples of the carboxy substituted C1-6 alkoxy group include a carboxymethyloxy group, a carboxyethyloxy group, a carboxypropyloxy group, a carboxybutyloxy group, a carboxypentyloxy group, a carboxyhexyloxy group and the like. The “carboxy substituted C1-20 alkoxy group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms in the C1-20 alkoxy group are substituted with carboxy groups. Examples of the carboxy substituted C1-20 alkoxy group include a carboxyheptyloxy group, a carboxyoctyloxy group, a carboxynonyloxy group, a carboxydecyloxy group, a carboxyundecyloxy group, a carboxydodecyloxy group, a carboxytridecyloxy group, a carboxytetradecyloxy group, a carboxypentadecyloxy group, a carboxyhexadecyloxy group, a carboxyheptadecyloxy group, a carboxyoctadecyloxy group, a carboxynonadecyloxy group, a carboxylcosadecyloxy group and the like, besides the aforementioned carboxy substituted C1-6 alkoxy groups.
Examples of the “C6-10 aryl group” in the aforementioned R1 and R2 include a phenyl group, a 1-naphthyl group, a 2-naphthyl group and the like.
Examples of the “C1-6 alkylsulfanyl group” in the aforementioned substituent groups α-1 and β-1 include a methylsulfanyl group, an ethylsulfanyl group, a n-propylsulfanyl group, an isopropylsulfanyl group, a n-butylsulfanyl group, an isobutylsulfanyl group, a sec-butylsulfanyl group, a tert-butylsulfanyl group, a n-pentylsulfanyl group, an isopentylsulfanyl group, a neopentylsulfanyl group, a tert-pentylsulfanyl group, a 1-ethylpropylsulfanyl group, a n-hexylsulfanyl group and the like.
The alkylene moiety of the “C1-6 alkylenedioxy group” in the aforementioned substituent group α-1 may be straight chain, branched chain, or any combinations of these. Examples of the C1-6 alkylenedioxy group include a 1,5-pentylenedioxy group, a 1,6-hexylenedioxy group, a 1,1,2,2-tetramethylethylenedioxy group and the like, besides C1-4 alkylenedioxy groups such as a methylenedioxy group, a 1,2-ethylenedioxy group, a 1,3-propylenedioxy group, a 1,4-butylenedioxy group, a 1,1-dimethymethylenedioxy group and the like.
The “carboxy substituted C1-6 alkyl group” in the aforementioned substituent groups α-1 and β-1 means a group in which one or more hydrogen atoms of the C1-6 alkyl group are substituted with carboxy groups. Examples of the carboxy substituted C1-6 alkyl group include a carboxymethyl group, a carboxyethyl group, a carboxypropyl group, a carboxybutyl group, a carboxypentyl group, a carboxyhexyl group and the like. The “carboxy substituted C1-10 alkyl group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms of the C1-10 alkyl group are substituted with carboxy groups. Examples of the carboxy substituted C1-10 alkyl group include a carboxymethyl group, a 1-carboxyethyl group, a 2-carboxyethyl group, a 3-carboxypropyl group, a 4-carboxybutyl group, a 5-carboxypentyl group, a 6-carboxyhexyl group, a 7-carboxyheptyl group, a 8-carboxyoctyl group, a 9-carboxynonyl group, a 10-carboxydecyl group and the like.
The “C3-8 cycloalkyl substituted C1-20 alkoxy group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms of the C1-20 alkoxy group are substituted with C3-8 cycloalkyl groups. Examples of the C3-8 cycloalkyl substituted C1-20 alkoxy group include a cyclopropylmethoxy group, a cyclobutylmethoxy group, a cyclopentylmethoxy group, a cyclohexylmethoxy group, a cycloheptylmethoxy group, a cyclooctylmethoxy group, a 1-(cyclohexyl)ethoxy group, a 2-(cyclohexyl)ethoxy group, a 3-(cyclohexyl)propoxy group, a 4-(cyclohexyl)butoxy group, a 5-(cyclohexyl)pentyloxy group, a 6-(cyclohexyl)hexyloxy group, a 7-(cyclohexyl)heptyloxy group, a 8-(cyclohexyl)octyloxy group, a 9-(cyclohexyl)nonyloxy group, a 10-(cyclohexyl)decyloxy group, a 11-(cyclohexyl)undecyloxy group, a 12-(cyclohexyl)dodecyloxy group, a 13-(cyclohexyl)tridecyloxy group, a 14-(cyclohexyl)tetradecyloxy group, a 15-(cyclohexyl)pentadecyloxy group, a 16-(cyclohexyl)hexadecyloxy group, a 17-(cyclohexyl)heptadecyloxy group, a 18-(cyclohexyl)octadecyloxy group, a 19-(cyclohexyl)nonadecyloxy group, a 20-(cyclohexyl)icosyloxy group and the like. The C3-8 cycloalkyl substituted C1-20 alkoxy group is preferably a C3-8 cycloalkyl substituted C1-10 alkoxy group, and more preferably a C3-8 cycloalkyl substituted C1-6 alkoxy group.
The “phenyl substituted C1-20 alkoxy group” means a group in which one or more hydrogen atoms of the C1-20 alkoxy group are substituted with phenyl groups. Examples of the phenyl substituted C1-20 alkoxy group include a benzyloxy group, a 1-phenylethoxy group, a 2-phenylethoxy group, a 3-phenylpropoxy group, a 4-phenylbutoxy group, a 5-phenylpentyloxy group, a 6-phenylhexyloxy group, a 7-phenylheptyloxy group, a 8-phenyloctyloxy group, a 9-phenylnonyloxy group, a 10-phenyldecyloxy group, a 11-phenylundecyloxy group, a 12-phenyldodecyloxy group, a 13-phenyltridecyloxy group, a 14-phenyltetradecyloxy group, a 15-phenylpentadecyloxy group, a 16-phenylhexadecyloxy group, a 17-phenylheptadecyloxy group, a 18-phenyloctadecyloxy group, a 19-phenylnonadecyloxy group, a 20-phenylicosyloxy group and the like. The phenyl substituted C1-20 alkoxy group is preferably a phenyl substituted C1-10 alkoxy group, and more preferably a phenyl substituted C1-6 alkoxy group.
The “hydroxy substituted C1-20 alkoxy group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms of the C1-20 alkoxy group are substituted with hydroxy groups. Examples of the hydroxy substituted C1-20 alkoxy group include a hydroxymethoxy group, a 1-hydroxyethoxy group, a 2-hydroxyethoxy group, a 3-hydroxypropoxy group, a 4-hydroxybutoxy group, a 5-hydroxypentyloxy group, a 6-hydroxyhexyloxy group, a 7-hydroxyheptyloxy group, a 8-hydroxyoctyloxy group, a 9-hydroxynonyloxy group, a 10-hydroxydecyloxy group, a 11-hydroxyundecyloxy group, a 12-hydroxydodecyloxy group, a 13-hydroxytridecyloxy group, a 14-hydroxytetradecyloxy group, a 15-hydroxypentadecyloxy group, a 16-hydroxyhexadecyloxy group, a 17-hydroxyheptadecyloxy group, a 18-hydroxyoctadecyloxy group, a 19-hydroxynonadecyloxy group, a 20-hydroxyicosyloxy group and the like. The hydroxy substituted C1-20 alkoxy group is preferably a hydroxy substituted C1-10 alkoxy group, and more preferably a hydroxy substituted C1-6 alkoxy group.
The “C1-6 alkoxy substituted C1-10 alkoxy group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms of the C1-10 alkoxy group are substituted with C1-6 alkoxy groups. Examples of the C1-6 alkoxy substituted C1-10 alkoxy group include a methoxymethoxy group, a 1-methoxyethoxy group, a 2-methoxyethoxy group, a 3-methoxypropoxy group, a 4-methoxybutoxy group, a 5-methoxypentyloxy group, a 6-methoxyhexyloxy group, a 7-methoxyheptyloxy group, a 8-methoxyoctyloxy group, a 9-methoxynonyloxy group, a 10-methoxydecyloxy group, an ethoxymethoxy group, an isopropoxymethoxy group, a tert-butoxymethoxy group and the like. The C1-6 alkoxy substituted C1-10 alkoxy group is preferably a C1-6 alkoxy substituted C1-6 alkoxy group.
The “phenoxy substituted C1-20 alkoxy group” in the aforementioned substituent group γ-1 means a group in which one or more hydrogen atoms of the C1-20 alkoxy group are substituted with phenoxy groups. Examples of the phenoxy substituted C1-20 alkoxy group include a phenoxymethoxy group, a 1-phenoxyethoxy group, a 2-phenoxyethoxy group, a 3-phenoxypropoxy group, a 4-phenoxybutoxy group, a 5-phenoxypentyloxy group, a 6-phenoxyhexyloxy group, a 7-phenoxyheptyloxy group, a 8-phenoxyoctyloxy group, a 9-phenoxynonyloxy group, a 10-phenoxydecyloxy group, a 11-phenoxyundecyloxy group, a 12-phenoxydodecyloxy group, a 13-phenoxytridecyloxy group, a 14-phenoxytetradecyloxy group, a 15-phenoxypentadecyloxy group, a 16-phenoxyhexadecyloxy group, a 17-phenoxyheptadecyloxy group, a 18-phenoxyoctadecyloxy group, a 19-phenoxynonadecyloxy group, a 20-phenoxyicosyloxy group and the like. The phenoxy substituted C1-20 alkoxy group is preferably a phenoxy substituted C1-10 alkoxy group, and more preferably a phenoxy substituted C1-6 alkoxy group.
The “di(C1-10 alkyl)amino group” in the aforementioned substituent group γ-1 means a group in which two hydrogen atoms of the amino group are substituted with C1-10 alkyl groups. Each of the two C1-10 alkyl groups of the (C1-10 alkyl)amino group may be the same or different. Examples of the di(C1-6 alkyl)amino group include a di(n-pentyl)amino group, a diisopentylamino group, a di(n-hexyl)amino group, a dicyclopentyl amino group, a dicyclohexylamino group, a di(n-heptyl)amino group, a di(n-octyl)amino group, a di(n-nonyl)amino group, a di(n-decyl)amino group and the like, besides di(C1-4 alkyl)amino groups such as a dimethylamino group, a diethylamino group, a methyl(ethyl)amino group, a di(n-propyl)amino group, a diisopropylamino group, a di(n-butyl)amino group, a diisobutylamino group, a di(sec-butyl)amino group, a dicyclopropylamino group, a dicyclobutylamino group, a di(cyclopropylmethyl)amino group and the like. The di(C1-10 alkyl)amino group is preferably a di(C1-6 alkyl)amino group.
Examples of the “5 to 7-membered completely saturated heterocyclic group (the heterocyclic group comprises one nitrogen atom as the ring-constituting atom and may further comprise one hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom as the ring-constituting atom, and the heterocyclic group binds to E via the nitrogen atom that is the ring-constituting atom” include a pyrrolidin-1-yl group, a pyrazolidin-1-yl group, an imidazolidin-1-yl group, an oxazolidin-3-yl group, a thiazolidin-3-yl group, a piperidin-1-yl group, a piperazin-1-yl group, a morpholin-4-yl group, a thiomorpholin-4-yl group, a hexahydro-1H-azepin-1-yl group, a hexahydro-1,4-diazepin-1-yl group, a hexahydro-1,4-oxazepin-4-yl group, a hexahydro-1,4-thiazepin-4-yl group and the like.
Examples of the “straight chain alkylene group” in the aforementioned Z1, Z2 and Z3 include a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, a hexane-1,6-diyl group, a heptane-1,7-diyl group, an octane-1,8-diyl group, a nonane-1,9-diyl group and a decane-1,10-diyl group. Examples of the “C1-3 straight chain alkylene group” in the aforementioned W′ include a methylene group, an ethylene group and a propane-1,3-diyl group.
Examples of the “C1-6 alkylsulfonyl group” in the aforementioned substituent group α-1 include a methylsulfonyl group, an ethylsulfonyl group, a n-propylsulfonyl group, an isopropylsulfonyl group, a n-butylsulfonyl group, an isobutylsulfonyl group, a sec-butylsulfonyl group, a tert-butylsulfonyl group, a n-pentylsulfonyl group, an isopentylsulfonyl group, a neopentylsulfonyl group, a tert-pentylsulfonyl group, a 1-ethylpropylsulfonyl group, a n-hexylsulfonyl group and the like. Examples of the “C1-6 alkylsulfonylamino group” in the aforementioned substituent group α-1 include a methylsulfonylamino group, an ethylsulfonylamino group, a n-propylsulfonylamino group, an isopropylsulfonylamino group, a n-butylsulfonylamino group, an isobutylsulfonylamino group, a sec-butylsulfonylamino group, a tert-butylsulfonylamino group, a n-pentylsulfonylamino group, an isopentylsulfonylamino group, a neopentylsulfonylamino group, a tert-pentylsulfonylamino group, a 1-ethylpropylsulfonylamino group, a n-hexylsulfonylamino group and the like.
Examples of the “C1-6 alkylcarbonyl group” in the aforementioned substituent group α-1 include an acetyl group, an ethylcarbonyl group, a n-propylcarbonyl group, an isopropylcarbonyl group, a n-butylcarbonyl group, an isobutylcarbonyl group, a sec-butylcarbonyl group, a tert-butylcarbonyl group, a n-pentylcarbonyl group, an isopentylcarbonyl group, a neopentylcarbonyl group, a tert-pentylcarbonyl group, a 1-ethylpropylcarbonyl group, a n-hexylcarbonyl group and the like.
The “halogenated C1-6 alkoxy substituted phenyl group” in the aforementioned substituent group β-1 means a group in which one or more hydrogen atoms of the phenyl group are substituted with halogenated C1-6 alkoxy groups. Examples of the halogenated C1-6 alkoxy substituted phenyl group include a chloromethoxyphenyl group, a bromomethoxyphenyl group, a fluoromethoxyphenyl group, a dichloromethoxyphenyl group, a dibromomethoxyphenyl group, a difluoromethoxyphenyl group, a trichloromethoxyphenyl group, a tribromomethoxyphenyl group, a trifluoromethoxyphenyl group, a 3,5-bistrifluoromethoxyphenyl group, a 2,2,2-trifluoroethoxyphenyl group, a pentafluoroethoxyphenyl group, a heptafluoropropoxyphenyl group, a nonafluorobutoxyphenyl group, a perfluoropentyloxyphenyl group, a perfluorohexyloxyphenyl group and the like.
The “C1-6 alkyl substituted phenyl group” in the aforementioned substituent group β-1 means a group in which one or more hydrogen atoms of the phenyl group are substituted with C1-6 alkyl groups. Examples of the C1-6 alkyl substituted phenyl group include a methylphenyl group, a dimethylphenyl group, an ethylphenyl group, a propylphenyl group, a butylphenyl group, a pentylphenyl group, a hexylphenyl group and the like.
The “carboxy substituted C2-6 alkenyl group” in the aforementioned substituent group β-1 means a group in which one or more hydrogen atoms of the C2-6 alkenyl group are substituted with carboxy groups. Examples of the carboxy substituted C2-6 alkenyl group include a carboxyvinyl group, a carboxyallyl group, a carboxypropenyl group, a carboxybutenyl group, a carboxypentenyl group and the like.
The compounds represented by the aforementioned formula (I) may form salts. Examples of pharmacologically acceptable salts include, when the compound has an acidic group, for example, metal salts such as a lithium salt, a sodium salt, a potassium salt, a magnesium salt, a calcium salt and the like, or ammonium salts such as an ammonium salt, a methylammonium salt, a dimethylammonium salt, a trimethylammonium salt, a dicyclohexylammonium and the like, and when the compound has a basic group, for example, mineral acid salts such as a hydrochloride, a hydrobromide, a hydrosulfate, a nitrate, a phosphate and the like, or organic acid salts such as a methane sulfonate, a benzene sulfonate, a para-toluene sulfonate, an acetate, a propionate, a tartrate, a fumarate, a maleate, a malate, an oxalate, a succinate, a citrate, a benzoate, a mandelate, a cinnamate, a lactate and the like. Salts may sometimes form with amino acids such as glycine and the like. As active ingredients of the medicament of the present invention, pharmacologically acceptable salts may also be suitably used.
The compounds represented by the aforementioned formula (I) or the salts thereof may exist as hydrates or solvates. As active ingredients of the medicament of the present invention, any of the aforementioned substances may be used. Furthermore, the compounds represented by the aforementioned formula (I) may sometimes have one or more asymmetric carbons, and may exist as steric isomers such as an optically active substance and a diastereomer. The active ingredients of the medicament of the present invention may be used in pure form of stereoisomers, an arbitrary mixture of enantiomers or diastereomers, and racemate.
Moreover, the compounds represented by the aforementioned formula (I) may exist as tautomers. The active ingredients of the medicament of the present invention may be used in pure form of tautomers or a mixture thereof. Furthermore, when the compounds represented by the formula (I) have olefinic double bonds, the configuration may be either E or Z, and the active ingredients of the medicament of the present invention may be uses in either of geometrical configurations or a mixture thereof.
Examples of the preferred compounds as the active ingredients of the medicaments of the present invention are shown in the following tables. However, the active ingredients of the medicaments of the present invention are not limited to those compounds. In the tables, (a) means that the bond at the left-hand end binds to E, and the bond at the right-hand end binds to the carboxy group. In the tables, (b) means that the bond at the left-hand end binds to G, and the bond at the right-hand end binds to R2. In the tables, (c) means that the compound was obtained as a sodium salt. In the tables, (d) means that the bond at the left-hand end binds to E, and the bond at the right-hand end binds to the 1H-tetrazol-5-yl group. In the tables, (e) means that the bond at the left-hand end binds to the nitrogen atom, and the bond at the right-hand end binds to the carboxy group. In the tables, (f) means that the bond at the left-hand end binds to the nitrogen atom, and the bond at the right-hand end binds to R2.
The compounds represented by the formula (I) can be prepared, for example, by the following methods.
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —V′—(V′)k—, and Y′ is a carboxy group, can be prepared by the following method:
wherein L1 represents a halogen atom or the like; L2 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; X represents the formula —V′—(V′)k—; R1, R2, E, G, V′, k and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (3) can be prepared by reacting the compound represented by the general formula (1) with the compound represented by the general formula (2). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Excessive amounts of base may preferably be used. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The final target compound represented by the general formula (5) can be prepared by reacting the compound represented by the general formula (3) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal complex, in the presence or absence of a phosphine ligand, in the presence or absence of a base, in a solvent. Examples of the transition metal complex include [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II), tetrakis(triphenylphosphine)palladium, palladium(II) acetate and tris(dibenzylideneacetone)dipalladium. Examples of the phosphine ligand include 2-(di-tert-butylphosphino)biphenyl and 2-dicyclohexylphoshino)biphenyl. Examples of the base include inorganic bases and organic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —V′—(V′)k—, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; X represents the formula —V′—(V′)k—; T represents —R″—; R1, R2, E, G, V′, k and M have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (7) can be prepared by reacting the compound represented by the general formula (3) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of copper(II) oxide, in the presence of a base, in a solvent. Examples of the base include inorganic bases. Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —V′—(V′)k—, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L2 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; X represents the formula —V′—(V′)k—; R1, R2, E, G, V′, k and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (9) can be prepared by reacting the compound represented by the general formula (8) with the compound represented by the general formula (2). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The compound represented by the general formula (10) can be prepared by reacting the compound represented by the general formula (9) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal complex, in the presence or absence of a phosphine ligand, in the presence or absence of a base, in a solvent. Examples of the transition metal complex include [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II), tetrakis(triphenylphosphine)palladium, palladium(II) acetate and tris(dibenzylideneacetone)dipalladium. Examples of the phosphine ligand include 2-(di-tert-butylphosphino)biphenyl and 2-dicyclohexylphoshino)biphenyl. Examples of the base include inorganic bases and organic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, alcohol type solvents, water, or a mixed solvent thereof.
The final target compound represented by the general formula (12) can be prepared by reacting the compound represented by the general formula (10) with the compound represented by the general formula (11). This reaction is carried out, for example, in the presence of an ammonium salt, in a solvent. Examples of the ammonium salt include ammonium chloride and triethylamine hydrochloride.
Examples of the solvent include amide type solvents.
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —V′—(V′)k—, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; X represents the formula —V′—(V′)k—; T is —R″—; R1, R2, E, G, V′, k and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (13) can be prepared by reacting the compound represented by the general formula (9) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of copper(II) oxide, in the presence of a base, in a solvent. Examples of the base include inorganic bases. Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The final target compound represented by the general formula (14) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (13) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is —CH═CH—, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L2 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R101 represents a C1-6 alkyl group or the like; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (16) can be prepared by reacting the compound represented by the general formula (15) with the compound represented by the general formula (2). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The compound represented by the general formula (17) can be prepared by reacting the compound represented by the general formula (16) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal complex, in the presence or absence of a phosphine ligand, in the presence or absence of a base. Examples of the transition metal complex include [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II), tetrakis(triphenylphosphine)palladium, palladium(II) acetate and tris(dibenzylideneacetone)dipalladium. Examples of the phosphine ligand include 2-(di-tert-butylphosphino)biphenyl and 2-dicyclohexylphoshino)biphenyl. Examples of the base include inorganic bases and organic bases. Examples of the solvent include ethers, amide type solvents, aromatic solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (18) can be prepared by reacting the compound represented by the general formula (17) with phosphonoacetic acid triester. This reaction is known as “Horner-Wadsworth-Emmons reaction,” and is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the phosphonoacetic acid trimester include triethyl phosphonoacetate and bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include ether type solvents, aromatic solvents, or a mixed solvent thereof. When this preparation method is carried out, the compounds wherein the double bond is in the E form are mainly obtained. If it is necessary to prepare the compounds wherein the double bond is in the Z form, it is preferable to use bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate, potassium bis(trimethylsilyl)amide and 18-Crown-6.
In the aforementioned Scheme 5, even if the order of the Steps 2 and 3 in the process are reversed, the compounds represented by the general formula (18) can be prepared.
The final target compound represented by the general formula (19) can be prepared by the hydrolysis of the compound represented by the general formula (18). This reaction is carried out, for example, in the presence of a base, in a solvent. The reaction may be carried out under ultrasonic irradiation. Examples of the base include inorganic bases. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof. When the aftertreatment is carried out under acidic condition, the free form of the carboxylic acid can be obtained. When the aftertreatment is carried out under basic condition, the salt of the carboxylic acid can be obtained.
The compounds represented by the aforementioned general formula (17) can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L3 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (21) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 5 except using the compound represented by the general formula (20) in place of the compound represented by the general formula (16).
The compound represented by the general formula (17) can be prepared by reacting the compound represented by the general formula (21) with the compound represented by the general formula (22). This reaction is carried out, for example, in the presence of a base, in a solvent. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, or a mixed solvent thereof.
In the aforementioned Scheme 6, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (17) can be prepared.
The compounds represented by the aforementioned general formula (19) can also be prepared, for example, by the following method:
wherein R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (19) can be prepared by reacting the compound represented by the general formula (17) with malonic acid. This reaction is carried out, for example, in the presence of a catalytic amount of an amine, in the presence or absence of a base, without a solvent or in a solvent. Examples of the amine include pyrrolidine, piperidine and the like. Examples of the base include organic bases. Examples of the solvent include alcohol type solvents, or a mixed solvent thereof. When this preparation method is carried out, the compounds wherein the double bond is in the E form are mainly obtained.
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is —CH═CH—, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; R101 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (24) can be prepared by reacting the compound represented by the general formula (16) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of copper(II) oxide, in the presence of a base, in a solvent. Examples of the base include inorganic bases. As the solvent, any solvent can be used as long as it does not inhibit the reaction, and examples include halogenated solvents, pyridine, or or a mixed solvent thereof.
The compound represented by the general formula (25) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 5 except using the compound represented by the general formula (24) in place of the compound represented by the general formula (17).
In the aforementioned Scheme 8, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (25) can be prepared.
The final target compound represented by the general formula (26) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (25) in place of the compound represented by the general formula (18). In the aforementioned Scheme 8, the compound represented by the general formula (26) can also be prepared by converting the formyl group of the compound represented by the general formula (16) into the corresponding acetal group, carrying out the reaction of the obtained acetal derivative in the same manner as the aforementioned Step 1, and then converting the acetal group into the corresponding formyl group.
The compounds represented by the aforementioned general formula (24), wherein -T-R1 exists in the ortho or para position with respect to the formyl group can also be prepared, for example, by the following method:
wherein L4 represents a halogen atom (preferably, a fluorine atom) or the like; R1, R2, T, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (24) can be prepared by reacting the compound represented by the general formula (27) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of a base, in a solvent, at a reaction temperature of 0° C. to 180° C. (preferably, at a temperature of 0° C. to the boiling point of the solvent). Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, or a mixed solvent thereof.
The compound represented by the aforementioned general formula (24) can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L3 represents a halogen atom or the like; R1, R2, T, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (28) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 8 except using the compound represented by the general formula (20) in place of the compound represented by the general formula (16).
The compound represented by the general formula (24) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 6 except using the compound represented by the general formula (28) in place of the compound represented by the general formula (21).
In the aforementioned Scheme 10, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (24) can be prepared.
The compounds represented by the aforementioned general formula (28) can also be prepared, for example, by the following method:
wherein L3 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1, T and E has the same meaning as the aforementioned definition.
The compound represented by the general formula (28) can be prepared by reacting the compound represented by the general formula (29) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of copper(II) acetate, in the presence of a base, in a solvent. Molecular Sieves may be added. Examples of the base include organic bases.
Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The compound represented by the aforementioned general formula (26) can also be prepared, for example, by the following method:
wherein R1, R2, T, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (26) can be prepared in the same manner as the aforementioned Scheme 7 except using the compound represented by the general formula (24) in place of the compound represented by the general formula (17).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is —CH═CH—, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (30) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 5 except using cyanomethylphosphonic acid diester in place of phosphonoacetic acid triester. Examples of the cyanomethylphosphonic acid diester include diethyl cyanomethylphosphonate.
The final target compound represented by the general formula (31) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (30) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is —CH═CH—, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (32) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 5 except using the compound represented by the general formula (24) in place of the compound represented by the general formula (17) and using cyanomethylphosphonic acid diester in place of phosphonoacetic acid triester. Examples of the cyanomethylphosphonic acid diester include diethyl cyanomethylphosphonate.
The final target compound represented by the general formula (33) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (32) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 1, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (34) can be prepared by the reduction of the double bond of the compound represented by the general formula (19). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal, under hydrogen atmosphere, in a solvent. Examples of the transition metal include palladium on activated carbon and platinum dioxide. When M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, n is 1, p is 0, q is 0, and r is 0, it is preferable to use platinum dioxide. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof. As it is obvious from the present preparation method, the compounds represented by the formula (I), wherein X is —CH═CH—, are useful as the synthetic intermediates for the compounds wherein X is the formula —V′—(V′)k—, V′ is a methylene group, and k is 1.
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 1, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (35) can be prepared in the same manner as the aforementioned Scheme 15 except using the compound represented by the general formula (26) in place of the compound represented by the general formula (19).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 1, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (36) can be prepared in the same manner as the aforementioned Scheme 15 except using the compound represented by the general formula (30) in place of the compound represented by the general formula (19).
The final target compound represented by the general formula (37) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (36) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 1, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (38) can be prepared in the same manner as the aforementioned Scheme 15 except using the compound represented by the general formula (32) in place of the compound represented by the general formula (19).
The final target compound represented by the general formula (39) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (38) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —N(R4)—C(═O)—, R4 is a hydrogen atom, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L2 represents a halogen atom or the like; L5 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (41) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 5 except using the compound represented by the general formula (40) in place of the compound represented by the general formula (15).
The compound represented by the general formula (42) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 5 except using the compound represented by the general formula (41) in place of the compound represented by the general formula (16).
The compound represented by the general formula (43) can be prepared by the reduction of the nitro group of the compound represented by the general formula (42). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal, under hydrogen atmosphere, in a solvent. Examples of the transition metal include palladium on activated carbon, platinum dioxide and Raney nickel. When M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, n is 1, p is 0, q is 0, and r is 0, it is preferable to use platinum dioxide. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The aforementioned reductive reduction of the nitro group can also be carried out in the presence of a metal or a metal halide, in the presence or absence of an acid, in a solvent. Examples of the metal include iron, tin and zinc. Examples of the metal halide include tin(II) chloride. Examples of the acid include inorganic acids and organic acids. Examples of the solvent include alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (45) can be prepared by reacting the compound represented by the general formula (43) with the compound represented by the general formula (44). This reaction is carried out, for example, in the presence of a base, in a solvent. Examples of the base include inorganic bases and organic bases. Examples of the solvent include halogenated solvents, ether type solvents, or a mixed solvent thereof.
The final target compound represented by the general formula (46) can be prepared by the hydrolysis of the compound represented by the general formula (45). This reaction is carried out, for example, in the presence of a base, in a solvent. The reaction may be carried out under ultrasonic irradiation. Examples of the base include inorganic bases. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof. When the aftertreatment is carried out under acidic condition, the free form of the oxamic acid can be obtained. When the aftertreatment is carried out under basic condition, the salt of the oxamic acid can be obtained. The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —N(R4)—V′—, R4 is a hydrogen atom, and Y′ is a carboxy group, can be prepared in the same manner as the aforementioned Steps 1 to 5 in the Scheme 19 except using the compound represented by the formula L5-V′—CO2R102 in place of the compound represented by the general formula (44).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is —N(R4)—C(═O)—, R4 is a C1-6 alkyl group, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein R4 represents a C1-6 alkyl group; L6 represents a halogen atom or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (48) can be prepared by reacting the compound represented by the general formula (45) with the compound represented by the general formula (47). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The final target compound represented by the general formula (49) can be prepared in the same manner as the aforementioned Step 5 in the Scheme 19 except using the compound represented by the general formula (48) in place of the compound represented by the general formula (45). The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —N(R4)—V′—, R4 is a C1-6 alkyl group, and Y′ is a carboxy group, can be prepared in the same manner as the aforementioned Steps 1 to 4 in the Scheme 19 and Steps 1 to 2 in the Scheme 20, except using the compound represented by the formula L5-V′—CO2R102 in place of the compound represented by the general formula (44).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is —N(R4)—C(═O)—, R4 is a hydrogen atom, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L5 represents a halogen atom; R102 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (50) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 8 except using the compound represented by the general formula (41) in place of the compound represented by the general formula (16).
The compound represented by the general formula (51) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 19 except using the compound represented by the general formula (50) in place of the compound represented by the general formula (42).
The compound represented by the general formula (52) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 19 except using the compound represented by the general formula (51) in place of the compound represented by the general formula (43).
The final target compound represented by the general formula (53) can be prepared in the same manner as the aforementioned Step 5 in the Scheme 19 except using the compound represented by the general formula (52) in place of the compound represented by the general formula (45). The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —N(R4)—V′—, R4 is a hydrogen atom, and Y′ is a carboxy group, can be prepared in the same manner as the aforementioned Steps 1 to 4 in the Scheme 21 except using the compound represented by the formula L5-V′—CO2R102 in place of the compound represented by the general formula (44).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is —N(R4)—C(═O)—, R4 is a C1-6 alkyl group, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein R4 represents a C1-6 alkyl group; L6 represents a halogen atom or the like; R102 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (54) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 20 except using the compound represented by the general formula (52) in place of the compound represented by the general formula (45).
The final target compound represented by the general formula (55) can be prepared in the same manner as the aforementioned Step 5 in the Scheme 19 except using the compound represented by the general formula (54) in place of the compound represented by the general formula (45). The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —N(R4)—V′—, R4 is a C1-6 alkyl group, and Y′ is a carboxy group, can be prepared in the same manner as the aforementioned Steps 1 to 3 in the Scheme 21 and Steps 1 to 2 in the Scheme 22, except using the compound represented by the formula L5-V′—CO2R102 in place of the compound represented by the general formula (44).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —(V′)k—R″—W′—, k is 1, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L2 represents a halogen atom or the like; L7 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R104 represents a C1-6 alkyl group or the like; R1, R2, E, G, M, R″, V′ and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (57) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 5 except using the compound represented by the general formula (56) in place of the compound represented by the general formula (15).
The compound represented by the general formula (58) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 5 except using the compound represented by the general formula (57) in place of the compound represented by the general formula (16).
In the aforementioned Scheme 23, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (58) can be prepared.
The compound represented by the general formula (59) can be prepared by the reduction of the carbonyl group of the compound represented by the general formula (58). This reaction is carried out, for example, in the presence of a reducing agent, in a solvent. Examples of the reducing agent include sodium borohydride, lithium borohydride, lithium aluminium hydride and diisobutylaluminium hydride. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (61) can be prepared by reacting the compound represented by the general formula (59) with the compound represented by the general formula (60). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The final target compound represented by the general formula (62) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the a compound represented by the general formula (61) in place of the compound represented by the general formula (18).
The compounds represented by the aforementioned general formula (58) can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L3 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R1, R2, E, G, R″ and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (64) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 5 except using the compound represented by the general formula (63) in place of the compound represented by the general formula (16).
The compound represented by the general formula (58) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 6 except using the compound represented by the general formula (64) in place of the compound represented by the general formula (21).
In the aforementioned Scheme 24, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (58) can be prepared.
The compounds represented by the formula (I), wherein m is 1, T is —R″—X is the formula —(V′)k—R″—W′—, k is 1, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L7 represents a halogen atom or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R104 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, G, M, R″, V′ and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (65) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 8 except using the compound represented by the general formula (57) in place of the compound represented by the general formula (16).
The compound represented by the general formula (66) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 23 except using the compound represented by the general formula (65) in place of the compound represented by the general formula (58).
The compound represented by the general formula (67) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 23 except using the compound represented by the general formula (66) in place of the compound represented by the general formula (59).
The final target compound represented by the general formula (68) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (67) in place of the compound represented by the general formula (18).
The compounds represented by the aforementioned general formula (65), wherein -T-R1 exist in the ortho or para position with respect to —C(═R″)—R103 can also be prepared, for example, by the following method:
wherein L4 represents a halogen atom (preferably, a fluorine atom) or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R1, R2, T, E, G, R″ and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (65) can be prepared in the same manner as the aforementioned Scheme 9 except using the compound represented by the general formula (69) in place of the compound represented by the general formula (27).
The compounds represented by the aforementioned general formula (65) can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L3 represents a halogen atom or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R1, R2, T, E, G, R″ and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (70) can be prepared in the same manner as to the aforementioned Step 1 in the Scheme 8 except using the compound represented by the general formula (63) in place of the compound represented by the general formula (16).
The compound represented by the general formula (65) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 6 except using the compound represented by the general formula (70) in place of the compound represented by the general formula (21).
In the aforementioned Scheme 27, even if the order of the Steps 1 and 2 in the processes are reversed, the compounds represented by the general formula (65) can be prepared.
The compounds represented by the aforementioned general formula (70) can also be prepared, for example, by the following method:
Wherein L3 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R103 represents a hydrogen atom, or a C1-6 alkyl group; R1, T, R″ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (70) can be prepared in the same manner as the aforementioned Scheme 11 except using the compound represented by the general formula (71) in place of the compound represented by the general formula (29).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —(V′)k—R″—W′—, k is 1, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; R1, R2, E, M, G, R″, V′ and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (73) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 23 except using the compound represented by the general formula (72) in place of the compound represented by the general formula (60).
The final target compound represented by the general formula (74) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (73) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —(V′)k—R″—W′—, k is 1, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; T represents —R″—; R1, R2, E, M, G, R″, V′ and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (75) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 23 except using the compound represented by the general formula (66) in place of the compound represented by the general formula (59) and using the compound represented by the general formula (72) in place of the compound represented by the general formula (60).
The final target compound represented by the general formula (76) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (75) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —(V′)k—R″—W′—, R″ is an oxygen atom, k is 0, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; R104 represents a C1-6 alkyl group or the like; R1, R2, E, M, G and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (77) can be prepared by reacting the compound represented by the general formula (17) with percarboxylic acid. This reaction is known as “Baeyer-Villiger oxidation,” and is carried out, for example, in a solvent. Examples of the percarboxylic acid include peracetic acid, m-chloroperbenzoic acid and the like. Examples of the solvent include halogenated solvents.
The compound represented by the general formula (78) can be prepared by the hydrolysis of the compound represented by the general formula (77). This reaction is carried out, for example, in the presence of an acid or a base, in a solvent. Examples of the acid include for example, inorganic acids and organic acids. Examples of the base include inorganic bases. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (79) can be prepared by reacting the compound represented by the general formula (78) with the compound represented by the general formula (60). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The final target compound represented by the general formula (80) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (79) in place of the compound represented by the general formula (18).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —(V′)k—R″—W′—, R″ is an oxygen atom, k is 0, and Y′ is a carboxy group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; R104 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, M, G and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (81) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 31 except using the compound represented by the general formula (24) in place of the compound represented by the general formula (17).
The compound represented by the general formula (82) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 31 except using the compound represented by the general formula (81) in place of the compound represented by the general formula (77).
The compound represented by the general formula (83) can be prepared in the same manner as to the aforementioned Step 3 in the Scheme 31 except using the compound represented by the general formula (82) in place of the compound represented by the general formula (78).
The final target compound represented by the general formula (84) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (83) in place of the compound represented by the general formula (18).
The compounds represented by the formula (I), wherein m is 1, T is a single bond, X is the formula —(V′)k—R″—W′—, R″ is an oxygen atom, k is 0, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; R1, R2, E, M, G and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (85) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 31 except using the compound represented by the general formula (72) in place of the compound represented by the general formula (60).
The final target compound represented by the general formula (86) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (85) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 1, T is —R″—, X is the formula —(V′)k—R″—W′—, R″ is an oxygen atom, k is 0, and Y′ is a 1H-tetrazol-5-yl group, can be prepared, for example, by the following method:
wherein L7 represents a halogen atom or the like; T represents —R″—; R1, R2, E, M, G and W′ have the same meanings as the aforementioned definitions.
The compound represented by the general formula (87) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 31 except using the compound represented by the general formula (82) in place of the compound represented by the general formula (78) and using the compound represented by the general formula (72) in place of the compound represented by the general formula (60).
The final target compound represented by the general formula (88) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 3 except using the compound represented by the general formula (87) in place of the compound represented by the general formula (10).
The compounds represented by the formula (I), wherein m is 0, G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H, and T is a single bond, can be prepared, for example, by the following method:
wherein L2 represents a halogen atom or the like; L5 represents a halogen atom; L8 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, E, j, h and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (90) can be prepared by reacting the compound represented by the general formula (89) with the compound represented by the general formula (44′). This reaction is carried out, for example, in the presence of a base, in a solvent. Examples of the base include inorganic bases and organic bases. Examples of the solvent include halogenated solvents, ether type solvents, or a mixed solvent thereof.
The compound represented by the general formula (91) can be prepared by reacting the compound represented by the general formula (90) with the compound represented by the general formula (2). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
In the aforementioned Scheme 35, even if the order of the Steps 1 and 2 in the process are reversed, the compounds represented by the general formula (91) can be prepared.
The compound represented by the general formula (92) can be prepared by reacting the compound represented by the general formula (91) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal complex, in the presence or absence of a phosphine ligand, in the presence or absence of a base, in a solvent. Examples of the transition metal complex include [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II), tetrakis(triphenylphosphine)palladium, palladium(II) acetate and tris(dibenzylideneacetone)dipalladium. Examples of the phosphine ligand include 2-(di-tert-butylphosphino)biphenyl and 2-dicyclohexylphoshino)biphenyl. Examples of the base include inorganic bases and organic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, alcohol type solvents, water, or a mixed solvent thereof.
In the aforementioned Scheme 35, even if the order of the Steps 2 and 3 in the process are reversed, the compounds represented by the general formula (92) can be prepared.
The final target compound represented by the general formula (93) can be prepared by the hydrolysis of the compound represented by the general formula (92). This reaction is carried out, for example, in the presence of a base, in a solvent. The reaction may be carried out under ultrasonic irradiation. Examples of the base include inorganic bases. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof. When the aftertreatment is carried out under acidic condition, the free form of the oxamic acid can be obtained. When the aftertreatment is carried out under basic condition, the salt of the oxamic acid can be obtained. The compounds represented by the formula (I), wherein m is 0, G is —(CH2)j—N—W′—CO2H, and T is a single bond, can be prepared in the same manner as the aforementioned Steps 1 to 4 in the Scheme 35 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compounds represented by the aforementioned general formula (92) can also be prepared by, for example, the following method:
wherein L2 represents a halogen atom or the like; L5 represents a halogen atom; L8 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, E, j, h and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (94) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 35 except using the compound represented by the general formula (89) in place of the compound represented by the general formula (90).
The compound represented by the general formula (95) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 35 except using the compound represented by the general formula (94) in place of the compound represented by the general formula (91).
The compound represented by the general formula (92) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 35 except using the compound represented by the general formula (95) in place of the compound represented by the general formula (89).
In the aforementioned Scheme 36, even if the order of the Steps 2 and 3 in the process are reversed, the compounds represented by the general formula (92) can be prepared. In the compound (92), the compound wherein the formula —C(═O)—(CH2)h—CO2R102 is substituted with the formula —W′—CO2R102 can be prepared can be prepared in the same manner as the aforementioned Steps 1 to 3 in the Scheme 36 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compounds represented by the aforementioned general formula (92) can also be prepared, for example, by the following method:
wherein L2 represents a halogen atom or the like; L5 represents a halogen atom; L9 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, E, j, h and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (97) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 35 except using the compound represented by the general formula (96) in place of the compound represented by the general formula (91).
The compound represented by the general formula (98) can be prepared by the reduction of the nitro group of the compound represented by the general formula (97). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal, under hydrogen atmosphere, in a solvent. Examples of the transition metal include palladium on activated carbon, platinum dioxide and Raney nickel. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The aforementioned reductive reaction of the nitro group can also be carried out in the presence of a metal or a metal halide, in the presence or absence of an acid, in a solvent. Examples of the metal include iron, tin and zinc. Examples of the metal halide include tin(II) chloride. Examples of the acid include inorganic acids and organic acids. Examples of the solvent include alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (99) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 35 except using the compound represented by the general formula (98) in place of the compound represented by the general formula (89).
The compound represented by the general formula (92) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 35 except using the compound represented by the general formula (99) in place of the compound represented by the general formula (90).
In the aforementioned Scheme 37, even if the order of the Steps 3 and 4 in the process are reversed, the compound represented by the general formula (92) can be prepared. In the compound (92), the compound wherein the formula —C(═O)—(CH2)h—CO2R102 is substituted with the formula —W′—CO2R102 can be prepared can be prepared in the same manner as the aforementioned Steps 1 to 4 in the Scheme 37 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compounds represented by the formula (I), wherein m is 0, G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H, T is a single bond, and M is a single bond, can also be prepared, for example, by the following method:
wherein L5 represents a halogen atom; Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; R1, R2, j, h and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (101) can be prepared by reacting the compound represented by the general formula (98) with the compound represented by the general formula (100). This reaction is carried out, for example, in the presence of copper(II) acetate, in the presence of a base, in a solvent. Molecular Sieves may be added. Examples of the base include organic bases. Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The compound represented by the general formula (102) can be prepared in the same manner as the aforementioned Step 1 the Scheme 35 except using the compound represented by the general formula (101) in place of the compound represented by the general formula (89).
The final target compound represented by the general formula (103) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 35 except using the compound represented by the general formula (102) in place of the compound represented by the general formula (92). In the compound (92), the compound wherein the formula —C(═O)—(CH2)h—CO2R102 is substituted with the formula —W′—CO2R102 can be prepared can be prepared in the same manner as the aforementioned Steps 1 to 3 in the Scheme 38 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compounds represented by the formula (I), wherein m is 0, G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H, and T is —R″—, can be prepared, for example, by the following method:
wherein L2 represents a halogen atom or the like; L5 represents a halogen atom; L10 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R102 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, E, j, h and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (105) can be prepared by reacting the compound represented by the general formula (104) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of copper(II) oxide, in the presence of a base, in a solvent. Examples of the base include inorganic bases (for example, potassium carbonate, sodium carbonate and sodium hydrogen carbonate). Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The compound represented by the general formula (106) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 37 except using the compound represented by the general formula (105) in place of the compound represented by the general formula (97).
The compound represented by the general formula (107) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 35 except using the compound represented by the general formula (106) in place of the compound represented by the general formula (89).
The compound represented by the general formula (108) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 35 except using the compound represented by the general formula (107) in place of the compound represented by the general formula (90).
The final target compound represented by the general formula (109) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 35 except using the compound represented by the general formula (108) in place of the compound represented by the general formula (92).
In the aforementioned Scheme 39, even if the order of the Steps 3 and 4 in the process are reversed, the compound represented by the general formula (108) can be prepared. The compounds represented by the formula (I), wherein m is 0, G is —(CH2)j—N—W′—CO2H, T is —R″—, can be prepared in the same manner as the aforementioned Steps 1 to 5 in the Scheme 39 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compounds represented by the aforementioned general formula (105) can also be prepared, for example, by the following method:
wherein L11 represents a halogen atom, a nitro group or the like; Z′ represents —(CH2)j—N; R1, T and j has the same meaning as the aforementioned definition.
The compound represented by the general formula (105) can be prepared by reacting the compound represented by the general formula (110) with the compound represented by the general formula (6). This reaction is carried out, for example, in the presence of a base, in a solvent. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, or a mixed solvent thereof.
The compounds represented by the aforementioned general formula (105) can also be prepared, for example, by the following method:
wherein Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1, T and j has the same meaning as the aforementioned definition.
The compound represented by the general formula (105) can be prepared by reacting the compound represented by the general formula (111) with the compound represented by the general formula (4). This reaction is carried out, for example, in the presence of copper(II) acetate, in the presence of a base, in a solvent. Molecular Sieves may be added. Examples of the base include organic bases. Examples of the solvent include halogenated solvents, pyridine, or a mixed solvent thereof.
The compounds represented by the formula (I), wherein m is 0, G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H, T is —R″—, and M is a single bond, can be prepared, for example, by the following method:
wherein L5 represents a halogen atom; Z′ represents —(CH2)j—N; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R102 represents a C1-6 alkyl group or the like; T represents —R″—; R1, R2, j, h and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (112) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 38 except using the compound represented by the general formula (106) in place of the compound represented by the general formula (98).
The compound represented by the general formula (113) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 35 except using the compound represented by the general formula (112) in place of the compound represented by the general formula (89).
The final target compound represented by the general formula (114) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 35 except using the compound represented by the general formula (113) in place of the compound represented by the general formula (92). The compounds represented by the formula (I), wherein m is 0, G is —(CH2)j—N—CO2H, T is —R″—, M is a single bond, can be prepared in the same manner as the aforementioned Steps 1 to 3 in the Scheme 42 except using the compound represented by the formula L5-W′—CO2R102 in place of the compound represented by the general formula (44′).
The compound represented by the following general formula (59a), which is the compound represented by the aforementioned general formula (59) wherein V′ is a methylene group substituted with one C1-6 alkyl group, can also be prepared, for example, by the following method:
wherein R5 represents a C1-6 alkyl group; Met represents lithium, —MgBr or the like; R1, R2, M, G, R″ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (59a) can be prepared by reacting the compound represented by the general formula (17) with the compound represented by the general formula (115). This reaction is carried out, for example, in a solvent. Examples of the R5-Met include a C1-6 alkyllithium and a C1-6 alkylmagnesium bromide. Examples of the solvent include ether type solvents, or a mixed solvent thereof.
The compound represented by the following general formula (66a), which is the compound represented by the aforementioned general formula (66) wherein V′ is a methylene group substituted with one C1-6 alkyl group, can also be prepared, for example, by the following method:
wherein R5 represents a C1-6 alkyl group; Met represents lithium, —MgBr or the like; R1, R2, T, M, G, R″ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (66a) can be prepared in the same manner as the aforementioned Scheme 43 except using the compound represented by the general formula (24) in place of the compound represented by the general formula (17).
The compound represented by the following general formula (94a), which is the compound represented by the aforementioned general formula (94) wherein M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, Q1 is a methylene group substituted with one group selected from the group consisting of a C1-6 alkyl group and a phenyl group, and n is 1 can also be prepared, for example, by the following method:
wherein L8 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R5 represents a C1-6 alkyl group, or a phenyl group; Met represents lithium, —MgBr or the like; R2, j, Q2, Q3, U′, p, q, r and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (117) can be prepared by reacting the compound represented by the general formula (89) with the compound represented by the general formula (116). This reaction is carried out, for example, in a solvent. Examples of the solvent include alcohol type solvents, or a mixed solvent thereof.
The compound represented by the general formula (94a) can be prepared by reacting the compound represented by the general formula (117) with the compound represented by the general formula (118). This reaction is carried out, for example, in a solvent. Examples of the R6-Met include a C1-6 alkyllithium, a phenyllithium, a C1-6 alkylmagnesium bromide and a phenylmagnesium bromide. Examples of the solvent include ether type solvents, or a mixed solvent thereof.
The compound represented by the following general formula (94b), which is the compound represented by the aforementioned general formula (94) wherein M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, Q1 is a methylene group, and n is 1, can also be prepared, for example, by the following method:
wherein L8 represents a halogen atom or the like; Z′ represents —(CH2)j—N; R2, j, Q2, Q3, U′, p, q, r and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (94b) can be prepared by the reduction of the imine of the compound represented by the general formula (117). This reaction is carried out, for example, in the presence of a reducing agent, in a solvent. Examples of the reducing agent include sodium borohydride, and lithium borohydride. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compounds represented by the general formula (42) can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; L3 represents a halogen atom or the like; R1, R2, E, G and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (119) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 5 except using the compound represented by the general formula (118) in place of the compound represented by the general formula (16).
The compound represented by the general formula (42) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 5 except using the compound represented by the general formula (119) in place of the compound represented by the general formula (22).
The compounds represented by the following general formula (98a), which is the compound represented by the aforementioned general formula (98) wherein Z′ is —(CH2)j—N, and j is 1, can also be prepared, for example, by the following method:
wherein L9 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1 and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (121) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 35 except using the compound represented by the general formula (120) in place of the compound represented by the general formula (91).
The compound represented by the general formula (98a) can be prepared by the reduction of the nitrile group of the compound represented by the general formula (121). This reaction is carried out, for example, in the presence of a reducing agent, in a solvent. Examples of the reducing agent include sodium borohydride, lithium borohydride and lithium aluminium hydride. Examples of the solvent include ether type solvents, alcohol type solvents, or a mixed solvent thereof.
The compounds represented by the following general formula (106a), which is the compound represented by the aforementioned general formula (106) wherein Z′ is —(CH2)j—N, and j is 1, can also be prepared, for example, by the following method:
wherein L10 represents a halogen atom or the like; R2, T and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (123) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 39 except using the compound represented by the general formula (122) in place of the compound represented by the general formula (104).
The compound represented by the general formula (106a) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 48 except using the compound represented by the general formula (123) in place of the compound represented by the general formula (121).
The compounds represented by the following general formula (24a), which is the compound represented by the aforementioned general formula (24) wherein G is an oxygen atom, and M is a single bond, can also be prepared, for example, by the following method:
wherein L1 represents a halogen atom or the like; R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1, R2, T and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (125) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 6 except using the compound represented by the general formula (6) in place of the compound represented by the general formula (22) and using the compound represented by the general formula (124) in place of the compound represented by the general formula (21).
The compound represented by the general formula (126) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 31 except using the compound represented by the general formula (125) in place of the compound represented by the general formula (17).
The compound represented by the general formula (127) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 31 except using the compound represented by the general formula (126) in place of the compound represented by the general formula (77).
The compound represented by the general formula (128) can be prepared by reacting the compound represented by the general formula (127) with hexamethylenetetramine. This reaction is known as “Duff reaction,” and is carried out in an organic acid (for example, acetic acid, trifluoroacetic acid and methanesulfonic acid) or an inorganic acid (for example, sulfuric acid. Furthermore, the compound represented by the general formula (128) can also be prepared, for example, by reactions such as Gatterman reaction, Reimee-Tiemann reaction and the like, that are known to those skilled in the art.
The compound represented by the general formula (24a) can be prepared in the same manner as the aforementioned Scheme 11 except using the compound represented by the general formula (128) in place of the compound represented by the general formula (29).
The compounds represented by the following general formula (82a), which is the compound represented by the aforementioned general formula (82) wherein G is an oxygen atom, and M is a single bond, can also be prepared, for example, by the following method:
wherein R100 represents a hydrogen atom, a C1-6 alkyl group or the like; R1, R2, T and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (130) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 5 except using benzyl halide in place of the compound represented by the general formula (2) and using the compound represented by the general formula (129) in place of the compound represented by the general formula (15).
The compound represented by the general formula (131) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 31 except using the compound represented by the general formula (130) in place of the compound represented by the general formula (17).
The compound represented by the general formula (132) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 31 except using the compound represented by the general formula (131) in place of the compound represented by the general formula (77).
The compound represented by the general formula (133) can be prepared in the same manner as the aforementioned Scheme 11 except using the compound represented by the general formula (132) in place of the compound represented by the general formula (29).
The compound represented by the general formula (82a) can be prepared by the deprotection of the benzyl group of the compound represented by the general formula (133). This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal, under hydrogen atmosphere, in a solvent. Examples of the transition metal include palladium on activated carbon, platinum dioxide and Raney nickel. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
In each of the aforementioned preparation methods, the compounds in the aforementioned formula (I) wherein T is a 1,4-piperazinylene, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)—, the formula —N(R′)C(═O)—, or the formula SO2N(R′)— can be prepared except using the compound wherein T is a 1,4-piperazinylene, —N(R′)—, the formula —CH2R″—, the formula —C(═O)N(R′)—, the formula —N(R′)C(═O)—, or the formula —SO2N(R′)— in place of the compound wherein T is —R″—.
The compounds represented by the following general formula (105a), which is the compound represented by the aforementioned general formula (105) wherein T is —CH2R″—, can be prepared, for example, by the following method:
wherein L100 represents a halogen atom or the like; R1, R″, Z′ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (105a) can be prepared by reacting the compound represented by the general formula (134) with the compound represented by the general formula (135). This reaction is carried out, for example, in the presence of a base, in a solvent. Crown ether may be added in the reaction. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
In each of the aforementioned preparation methods, the compounds in the aforementioned formula (I) wherein X is a single bond or —C(═O)— can be prepared except using the compound wherein X is a single bond or —C(═O)— in place of the compound wherein X is —CH═CH—, the formula —V′—(V′)k—, the formula —N(R4)—C(═O)—, the formula —N(R4)—V′—, or the formula —(V′)k—R″—W′—.
The compounds represented by the formula (I), wherein T is the formula —N(R′)C(═O)—, and Y′ is a carboxy group, can be prepared, by the following method:
in the formula, when m is 1, G′ represents a single bond, an oxygen atom, —C(═O)—, or a sulfur atom; when m is 0, G′ represents the formula —(CH2)j—N—C(═O)—(CH2)h—CO2R105, or the formula —(CH2)j—N—W′—CO2R105; Y″ represents the formula —CO2R105; R105 represents an alkyl group or the like; R1, R2, X, Y′, W′, E, h, j and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (138) can be prepared by reacting the compound represented by the general formula (136) with the compound represented by the general formula (137). This reaction is carried out in the presence of a condensing agent, in the presence or absence of a base, in a solvent. Examples of the condensing agent include phosphorus oxychloride, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, dicyclohexylcarbodiimide. Examples of the base include organic bases. Examples of the solvent include halogenated solvents, ether type solvents, aromatic solvents, or a mixed solvent thereof.
The final target compound represented by the general formula (139) can be prepared by the hydrolysis of the ester group (the formula —CO2R105) of the compound represented by the general formula (138). This reaction is carried out in the presence of a inorganic acid or a inorganic base, in a solvent. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compounds represented by the formula (I), wherein T is the formula —C(═O)—N(R′)— or the formula —SO2N(R′)—, and Y′ is a carboxy group, can be prepared, by the following method:
wherein T′ represents —C(═O)— or —SO2—, in the formula; when m is 1, G′ represents a single bond, an oxygen atom, —C(═O)—, or a sulfur atom; when m is 0, G′ represents the formula —(CH2)j—N—C(═O)—(CH2)h—CO2R105, or the formula —(CH2)j—N—W′—CO2R105; Y″ represents the formula —CO2R105; R105 represents an alkyl group or the like; R1, R2, X, Y′, W′, E, h, j and M have the same meanings as the aforementioned definitions.
The compound represented by the general formula (142) can be prepared by reacting the compound represented by the general formula (140) with the compound represented by the general formula (141). This reaction is carried out in the presence of a base, in a solvent. Examples of the condensing agent include phosphorus oxychloride, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, dicyclohexylcarbodiimide. Examples of the base include inorganic bases and organic bases. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, water, or a mixed solvent thereof.
The final target compound represented by the general formula (143) can be prepared in the same manner as the aforementioned Scheme 53 except using the compound represented by the general formula (142) in place of the compound represented by the general formula (138).
The compounds represented by the formula (I), wherein m is 1, and Y′ is a carboxy group, can also be prepared, by the following method:
wherein R1, R2, M, G, T, X and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (145) can be prepared by the hydrolysis of the cyano group of the compound represented by the general formula (144). This reaction is carried out in the presence of an acid or a base, without a solvent or in a solvent. Examples of the acid include inorganic acids. Examples of the base include inorganic bases. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compounds represented by the formula (I), wherein m is 1, X is the formula —V′—(V′)k—, —V′— is a methylene group substituted with one group selected from the substituent group δ-1, k is 1, and Y′ is a carboxy group, can also be prepared, by the following method:
wherein R5 represents a C1-6 alkyl group; Met represents lithium, —MgBr or the like; R1, R2, M, G, T and E have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (147) can be prepared by reacting the compound represented by the general formula (146) with the compound represented by the general formula (115). This reaction is known as “Michael addition reaction,” and is carried out in a solvent. Examples of the R5-Met include a C1-6 alkyllithium and a C1-6 alkylmagnesium bromide. Examples of the solvent include ether type solvents. The compound represented by (R5)2CuLi (Gilman reagent) may be used in place of the compound represented by the general formula (115).
The compounds represented by the formula (I), wherein m is 1, X is a single bond, and Y′ is a carboxy group, can also be prepared, by the following method:
wherein R1, R2, M, G, T and E have the same meanings as the aforementioned definitions.
The final target compound represented by the general formula (149) can be prepared by the oxidation of the formyl group of the compound represented by the general formula (148). This reaction is carried out, for example, in the presence of an oxidation agent, in a solvent. Examples of the oxidation agent include chlorous acid and potassium permaganate. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The compounds represented by the following general formula (154), which is the compound represented by the aforementioned general formulas (78) or (82) wherein G is —C(═O)—, and M is a single bond, can also be prepared, by the following method:
wherein R500 represents a protecting group of the hydroxy group (for example, a tri(C1-6 alkyl)silyl group, a benzyl group or the like); T represents a single bond or R″; R1, R2, R″ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (152) can be prepared by reacting the compound represented by the general formula (150) with the compound represented by the general formula (151). This reaction is carried out, for example, in the presence of a base, in a solvent. Examples of the base include organometallic bases. Examples of the solvent include halogenated solvents, ether type solvents, or a mixed solvent thereof.
The compound represented by the general formula (153) can be prepared by the oxidation of the compound represented by the general formula (152). This reaction is carried out, for example, in the presence of an oxidation agent, in a solvent. Examples of the oxidation agent include pyridinium dichromate, pyridinium chlorochromate, manganese dioxide and potassium permanganate. Examples of the solvent include halogenated solvents, ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
The compound represented by the general formula (154) can be prepared by the deprotection of the protecting group of the hydroxy group of the compound represented by the general formula (153). Examples of the deprotection reaction include methods described in T. W. Greene and P. G. M. Wuts; Protective Groups in Organic Synthesis, 3rd Ed., 1999.
The compounds represented by the following general formula (154), which is the compound represented by the aforementioned general formulas (78) or (82) wherein G is a single bond, and M is the formula -(Q1)n-(Q2)p-(Q3)r-(U′)q—, the formula -(Q1)n-(Q2)p-(U′)q-(Q3)r- or the formula -(Q1)n-(U′)q-(Q2)p-(Q3)r-, each of Q1, Q2 and Q3 is a methylene group, the sum of n, p, q and r is 1, and q is 0, can also be prepared, by the following method:
wherein R500 represents a protecting group of the hydroxy group (for example, a tri(C1-6 alkyl)silyl group, a benzyl group or the like); T represents a single bond or R″; R1, R2, R″ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (155) can be prepared by the reduction of the carbonyl group of the compound represented by the general formula (153) to the methylene group. This reaction is carried out, for example, in the presence of a catalytic amount of a transition metal, in the presence or absence of an acid, under hydrogen atmosphere, in a solvent. Examples of the transition metal complex include inorganic acids and organic acids. Examples of the acid include palladium on activated carbon and platinum dioxide. Examples of the solvent include ether type solvents, alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (156) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 58 except using the compound represented by the general formula (155) in place of the compound represented by the general formula (153).
The compounds represented by the following general formula (159), which is the compound represented by the aforementioned general formulas (95) or (112) wherein Z′ is —(CH2)j—N, and j is 1, can also be prepared, by the following method:
wherein R1, R2, M′ and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (159) can be prepared by reacting the compound represented by the general formula (157) with the compound represented by the general formula (158). This reaction is carried out, for example, in the presence of a reducing agent, in a solvent. An acid may be added. Examples of the reducing agent include sodium triacetoxyborohydride. Examples of the solvent include halogenated solvents, ether type solvents, or a mixed solvent thereof. In the Scheme 60, the reaction can also be carried out for the compound wherein R1 is substituted with R1-T-.
The compounds represented by the formula (I), wherein m is 1, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 0, and Y′ is a carboxy group, can also be prepared, by the following method:
wherein R10 represents a C1-6 alkyl group or the like; T represents a single bond or R″; R1, R2, M, G and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (162) can be prepared by reacting the compound represented by the general formula (160) with the compound represented by the general formula (161). This reaction is carried out, for example, in the presence of a base, in a solvent. An organic salt may also be used in place of the base. Examples of the base include inorganic bases. Examples of the organic salt include benzyltrimethylammonium hydroxide. Examples of the solvent include ether type solvents, alcohol type solvents, or a mixed solvent thereof.
The compound represented by the general formula (164) can be prepared by reacting the compound represented by the general formula (162) with the compound represented by the general formula (163). This reaction is carried out, for example, in the presence of an acid, in a solvent. Examples of the acid include inorganic acids. Examples of the solvent include alcohol type solvents, water, or a mixed solvent thereof.
The final target compound represented by the general formula (165) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (164) in place of the compound represented by the general formula (18).
The compounds represented by the formula (I), wherein m is 1, X is —C(═O)—, and Y′ is a carboxy group, can be prepared, by the following method:
wherein L3 represents a halogen atom or the like; R10 represents a C1-6 alkyl group or the like; T represents a single bond or R″; R1, R2, M, G and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (167) can be prepared in the same manner as the aforementioned Step 2 in the Scheme 10 except using the compound represented by the general formula (166) in place of the compound represented by the general formula (28).
The compound represented by the general formula (168) can be prepared in the same manner as the aforementioned Step 1 in the Scheme 61 except using the compound represented by the general formula (167) in place of the compound represented by the general formula (160).
The compound represented by the general formula (169) can be prepared by reacting the compound represented by the general formula (168) with the compound represented by the general formula (163). This reaction is carried out, for example, in the presence of copper(II) chloride dihydrate, in a solvent. Examples of the solvent include alcohol type solvents, water, or a mixed solvent thereof.
The final target compound represented by the general formula (170) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (169) in place of the compound represented by the general formula (18). In the Scheme 62, the reaction can also be carried out for the compound wherein R1 is substituted with R1-T-.
The compounds represented by the formula (I), wherein m is 1, X is the formula —V′—(V′)k—, V′ is a methylene group, k is 2, and Y′ is a carboxy group, can also be prepared, by the following method:
wherein R101 represents a C1-6 alkyl group or the like; T represents a single bond or R″; R1, R2, R″, M, G and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (172) can be prepared by reacting the compound represented by the general formula (160) with the compound represented by the general formula (171). This reaction is known as “Wittig reaction,” and is carried out in the presence of a base, in a solvent. Examples of the base include inorganic bases, organic bases and organometallic bases. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, or a mixed solvent thereof.
The compound represented by the general formula (173) can be prepared by the hydrolysis of the compound represented by the general formula (172). This reaction is carried out, for example, in the presence of an acid, in a solvent. Examples of the acid include inorganic acids and organic acids. Examples of the solvent include alcohol type solvents, water, or a mixed solvent thereof.
The compound represented by the general formula (174) can be prepared in the same manner as the aforementioned Step 3 in the Scheme 5 except using the compound represented by the general formula (173) in place of the compound represented by the general formula (17).
The compound represented by the general formula (175) can be prepared in the same manner as the aforementioned Scheme 15 except using the compound represented by the general formula (174) in place of the compound represented by the general formula (19).
The final target compound represented by the general formula (176) can be prepared in the same manner as the aforementioned Step 4 in the Scheme 5 except using the compound represented by the general formula (175) in place of the compound represented by the general formula (18).
The compounds represented by the general formula (4), wherein R100 is a hydrogen atom, can be prepared, for example, by the method described in J. Org. Chem., vol. 55, No. 15, pp. 4622-4634 (1990).
The compounds represented by the general formula (144) can also be prepared by the following method:
wherein T represents a single bond or R″; R1, R2, R″, M, G and E have the same meanings as the aforementioned definitions.
The compound represented by the general formula (178) can be prepared by the substitution of the hydroxy group of the compound represented by the general formula (177) with the halogen atom. This reaction is carried out, for example, in the presence of thionyl chloride, without a solvent or in a solvent. Examples of the solvent include halogenated solvents, ether type solvents, aromatic solvents, or a mixed solvent thereof.
The compound represented by the general formula (144) can be prepared by reacting the compound represented by the general formula (178) with a cyanide. This reaction is carried out in a solvent. Examples of the cyanide include sodium cyanide and potassium cyanide. Examples of the solvent include ether type solvents, amide type solvents, aromatic solvents, ketone type solvents, acetonitrile, or a mixed solvent thereof.
In each of the aforementioned preparation methods, examples of the inorganic base include lithium hydride, sodium hydride, potassium hydride, cesium carbonate, potassium carbonate, sodium carbonate, sodium hydrogen carbonate, sodium hydroxide, potassium hydroxide, potassium carbonate, sodium carbonate and potassium fluoride. Examples of the organic base include pyridine, triethylamine and diisopropylethylamine. Examples of the organometallic base include potassium tert-butoxide, lithium diisopropylamide and n-butyllithium. Examples of the inorganic acid include hydrochloric acid and sulfuric acid. Examples of the organic acid include acetic acid, trifluoroacetic acid and methanesulfonic acid. Examples of the crown ether include 18-crown-6. Examples of the Molecular Sieves include Molecular Sieves 4A. Examples of the halogenated solvent include dichloromethane, dichloroethane and chloroform. Examples of the ether type solvent include tetrahydrofuran, 1,2-dimethoxyethane and 1,4-dioxane. Examples of the amide type solvent include dimethylformamide and N-methylpyrrolidone. Examples of the aromatic solvent include benzene and toluene. Examples of the ketone type solvent include acetone and 2-butanone. Examples of the alcohol type solvent include methanol and ethanol.
The compound in the formula (I), in which m is 0, and G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H or the formula —(CH2)j—N—W′—CO2H, can be prepared from the compound in the formula (I), in which m is 0, and G is the formula —(CH2)j—N—C(═O)—(CH2)h-A or the formula —(CH2)j—N—W′-A (in each of the formulas, A represents a protecting group of the carboxylic acid). Therefore, the compound in the formula (I), in which m is 0, and G is the formula —(CH2)j—N—C(═O)—(CH2)h-A or the formula —(CH2)j—N—W′-A, is useful as a synthetic intermediate of the compound in the general formula (I), in which m is 0, and G is the formula —(CH2)j—N—C(═O)—(CH2)h—CO2H or the formula —(CH2)jN—W′—CO2—H.
Furthermore, the compound in the formula (I), in which m is 1, and Y′ is a carboxy group, can be prepared from the compound in the formula (I), in which m is 1, and Y′ is a protecting group of the carboxy group. Therefore, the compound in the general formula (I), in which m is 1, and Y′ is a carboxy group, is useful as a synthetic intermediate of the compound in the general formula (I), in which m is 1, and Y′ is a carboxy group.
In the formula (I), when m is 0, and G is the formula —(CH2)j—N—C(═O)—(CH2)h-A or the formula —(CH2)j—N—W′-A, then examples of A include, more specifically, ester groups such as the formula —CO2R105 and the like.
In the formula (I), when m is 1, and Y′ is a protecting group of the carboxy group, then examples of Y′ include, more specifically, a cyano group, ester groups such as the formula —CO2R105 and the like, and amide groups such as the formula —C(═O)—N(R106)(R107) and the like.
R105 represents an alkyl group (preferably a C1-10 alkyl group, further preferably a C1-6 alkyl group), a C6-10 aryl group, a C6-10 aryl substituted alkyl group (preferably a C6-10 aryl substituted C1-10 alkyl group, further preferably a phenyl substituted C1-6 alkyl group) or the like.
Each of R106 and R107 independently represents a hydrogen atom, an alkyl group (preferably a C1-10 alkyl group, further preferably a C1-6 alkyl group), a C6-10 aryl group, a C6-10 aryl substituted alkyl group (preferably a C6-10 aryl substituted C1-10 alkyl group, further preferably a phenyl substituted C1-6 alkyl group) or the like.
The compound represented by the formula (I) which is an active ingredient of the present invention, a salt thereof, a hydrate of the compound, a hydrate of the salt, a solvate of the compound, or a solvate of the salt can be prepared by using various known synthetic methods, taking advantage of the characteristics based on their basic structure or on the type of their substituent. Depending on the type of the functional group, it can be effective for the production technique for the compounds to protect it with a suitable protective group, or substitute it with a group readily convertible into the functional group, in the starting material or in the intermediate. The functional group includes, for example, amino group, hydroxyl group, and carboxyl group; and their protective groups are described, for example, in T. W. Greene and P. G. M. Wuts; Protective Groups in Organic Synthesis, 3rd Ed., 1999. Depending on the reaction condition, they may be suitably selected and used. Specifically the reaction is conducted after a protective group is introduced into the starting compound, and then optionally the protective group may be removed or may be converted into a desired group to thereby obtain the intended compound.
In the examples of the specification, methods for preparing typical compounds included in the formula (I) are explained in details. Therefore, those skilled in the art can prepare any compound included in the formula (I) by referring to the explanations of the aforementioned general preparation methods and of the specific preparation methods of the examples, selecting appropriate reaction starting materials, reaction reagents, and reaction conditions, and, if necessary, by adding appropriate modification and alteration of these methods.
The medicament of the present invention can be used for prevention and/or therapeutic treatment of a disease caused by an expression of PAI-1 or an enhancement of PAI-1 activity. The term “therapeutic treatment” used in the present specification includes prevention of progression of disease and the term “prevention” includes prevention of reoccurrence. The medicament of the present invention can be used as a medicament for prevention and/or therapeutic treatment of a disease caused by, for example, thrombus formation, fibrosis, visceral fat deposition, angiogenesis, deposition and remodeling of extracellular matrix, diseases caused by the proliferation, migration, infiltration and metastasis of cells (for example, tumor cells, vascular endothelial cells and the like), and the remodeling of tissues (for example, heart remodeling, vascular remodeling and the like).
More specifically, the medicament of the present invention can be used as a medicament for prevention and/or therapeutic treatment of one or more diseases selected from ischemic cerebrovascular diseases such as cerebral thrombosis, cerebral embolism, cerebral infarction, transient ischemic attack, cerebral stroke, cerebrovascular dementia and the like; Alzheimer's disease; Parkinson's disease; Huntington's disease; dementias such as cerebrovascular dementia, senile dementia and the like; ischemic heart diseases such as angina, myocardial infarction, intra-atrial thrombosis caused by atrial fibrillation, heart failure and the like; thrombotic pulmonary diseases such as pulmonary thrombosis, pulmonary embolism and the like; occlusive venous diseases such as deep-vein thrombosis (DVT), thrombophlebitis and the like; occlusive peripheral arterial diseases such as acute arterial occlusion, chronic arterial occlusion and the like; thrombus after bypass vascular transplantation; disseminated intravascular coagulation (DIC); acute coronary occlusion and restenosis after percutaneous transluminal coronary angioplasty (PTCA); angiopathy and thrombus caused by immune disorders such as antiphospholipid antibody syndrome and the like; angiopathy and thrombus caused by congenital thrombotic tendency such as genetic abnormality; thrombotic renal diseases such as renal thrombosis, renal embolism and the like; nephropathy caused by metabolic diseases; arteriosclerosis; thrombotic diseases, thrombosis, fibrosis, blood coagulation, ischemic diseases, heart attack, profound thrombosis, pulmonary thromboembolism, venous thromboembolism, nephrosclerosis, metabolic syndrome, aldosterone tissue disorder, organ failure, economy-class syndrome, endotoxic shock, allergic diseases, vascular events of the brain, the heart and the like, vasculitis, nonbacterial thrombotic endocarditis; severe infections such as sepsis and the like; fibrin-dependent pain in arthritis; diabetic complications such as retinopathy, nephropathy, neurosis, peripheral circulatory disturbance and the like; hypertension; diabetes; hyperinsulinemia; hypercholesterolemia; insulin-resistant disorder; hyperlipidemia; obesity; aging; polycystic ovarian syndrome; autoimmune diseases such as multiple sclerosis and the like; tumors including solid cancers such as lung cancer, pancreatic cancer, colon cancer, gastric cancer, prostate cancer, breast cancer, cervical cancer, ovarian cancer and the like; tumor invasion; tumor metastasis; asthma; endometriosis; age-related macular degeneration; fibrosis of tissues and the corresponding diseases such as prostatic hyperplasia, liver cirrhosis, pulmonary fibrosis, renal fibrosis, interstitial cystitis and the like; atherosclerosis; prevention of restenosis after placement of stent(s); prevention of thrombus formation and thrombosis after implantation of medical device(s) such as artificial joint, artificial blood vessel, artificial heart-lung machine, artificial heart and the like; scar after surgery; prevention of an adhesion of tissues; and acute rejections and arterial lesions after transplantation of the tissue(s) such as heart, kidney or (and) the like. Moreover, since the medicament of the present invention can prevent and improve thrombus formation, it is effective for wound healing and decubitus healing.
As the active ingredient of the medicament on the present invention, one or more kinds of substances selected from the group consisting of the compound represented by the formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof may be used. As the medicament of the present invention, the aforementioned substance, per se, may be used. However, preferably, the medicament of the present invention is provided in the form of a pharmaceutical composition comprising the aforementioned substance which is an active ingredient together with one or more pharmacologically acceptable pharmaceutical additives. In the aforementioned pharmaceutical compositions, a ratio of the active ingredient to the pharmaceutical additives is approximately 1 weight % to 90 weight %.
The medicament of the present invention may be administered as pharmaceutical compositions for oral administration, for example, granules, subtilized granules, powders, hard capsules, soft capsules, syrup, emulsion, suspension, or solution, or may be administered as pharmaceutical compositions for parenteral administration, for example, injections for intravenous administration, intramuscular administration or subcutaneous administration, drops, suppositories, percutaneous absorbent, transmucosal absorption preparations, nasal drops, ear drops, eye drops, and inhalations. Preparations made as pharmaceutical compositions in a form of powder may be dissolved when necessary and used as injections or drip infusions.
For preparation of pharmaceutical compositions, solid or liquid pharmaceutical additives may be used. Pharmaceutical additives may either be organic or inorganic. When an oral solid preparation is prepared, an excipient is added to the principal agent, and further binders, disintegrator, lubricant, colorant, flavoring agent are added if necessary, preparations in the forms of tablets, coating tablets, granules, powders, capsules and the like may be manufactured by common procedures. Examples of the excipient include lactose, sucrose, saccharose, glucose, corn starch, starch, talc, sorbit, crystal cellulose, dextrin, kaolin, calcium carbonate, and silicon dioxide. Examples of the binder include, for example, polyvinyl alcohol, polyvinyl ether, ethyl cellulose, methyl cellulose, gum Arabic, tragacanth, gelatine, shellac, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, calcium citrate, dextrin, and pectin. Examples of the lubricant include, for example, magnesium stearate, talc, polyethylene glycol, silica, and hydrogenated vegetable oil. As the coloring agent, any material can be used that are approved to be added to ordinary pharmaceuticals. As the flavoring agent, cocoa powder, menthol, aromatic acid, mint oil, borneol, cinnamon powder and the like can be used. These tables and granules may be applied with sugarcoating, gelatine coating, or an appropriate coating, if necessary. Preservatives, antioxidant and the like may be added, if required.
For the preparation of liquid preparations for oral administration such as emulsions, syrups, suspensions, and solutions, commonly used inactive diluents, for example, water or vegetable oil may be used. For these preparations, besides inactive diluents, adjuvants such as wetting agents, suspending aids, sweeting agents, flavoring agents, coloring agents or preservatives may be blended. After a liquid preparation is manufactured, the preparation may be filled in capsules made of a absorbable substance such as gelatin. Examples of solvents or suspending agents used for the preparations of parenteral administration such as injections or suppositories include, for example, water, propylene glycol, polyethylene glycol, benzyl alcohol, ethyl oleate, and lecithin. Examples of base materials used for preparation of suppositories include, for example, cacao butter, emulsified cacao butter, lauric fat, and witepsol. Methods for preparation of the aforementioned preparations are not limited, and any method ordinarily used in the art may be used.
When the preparations are prepared in the form of injections, carriers such as, for example, diluents including water, ethanol, macrogol, propyleneglycol, citric acid, acetic acid, phosphoric acid, lactic acid, sodium lactate, sulfuric acid and sodium hydroxide, pH modifiers and buffer solutions including sodium citrate, sodium acetate and sodium phosphate, stabilizers such as sodium pyrosulfite, ethylenediaminetetraacetic acid, thioglycolic acid and thiolactate may be used. For the preparation, a sufficient amount of a salt, glucose, mannitol or glycerin may be blended in the preparation to manufacture an isotonic solution, and an ordinary solubilizer, a soothing agent, or a topical anesthetic may be used.
When the preparation in the form of an ointment such as a paste, a cream, and a gel is manufactured, an ordinarily used base material, a stabilizer, a wetting agent, and a preservative may be blended, if necessary, and may be prepared by mixing the components by a common method. As the base material, for example, white petrolatum, polyethylene, paraffin, glycerin, cellulose derivatives, polyethylene glycol, silicon, and bentonite may be used. As the preservative, paraoxy methyl benzoate, paraoxy ethyl benzoate, paraoxy propyl benzoate and the like may be used. When the preparation in the form of a patch is manufactured, the aforementioned ointment, cream, gel, or paste and the like may be applied by a common method to an ordinary support. As the support, fabric or nonwoven fabric made of cotton, span rayon, synthetic fibers or and the like; and a film or a foam sheet such as made of soft vinyl chloride, polyethylene, and polyurethane and the like may be preferably used.
A dose of the medicament of the present invention is not particularly limited. For oral administration, a dose may generally be 0.01 to 5,000 mg per day for an adult as the weight of the compound of the present invention. It is preferred to increase or decrease the aforementioned dose appropriately depending on the age, pathological conditions, and symptoms of a patient. The aforementioned dose may be administered once a day or 2 to 3 times a day as divided portions with proper intervals, or intermittent administration for every several days may be acceptable. When the medicament is used as an injection, the dose may be 0.001 to 100 mg per day for an adult as the weight of the compound of the present invention.
Oral or parenteral administration of the medicament of the present invention may be carried out preoperatively, when the medicament of the present invention is used for prophylactic and/or therapeutic treatment of intravascular lesions after vascular transplantation or organ transplantation or after blood circulation restoration, whose examples include, for example, thrombus after bypass vascular transplantation, acute coronary occlusion and restenosis after PTCA, arterial lesions after organ transplantation such as cardiac transplantation and renal transplantation and the like. Furthermore, oral or parenteral administration of the medicament of the present invention may be carried out intraoperatively and/or postoperatively in addition to the aforementioned preoperative administration, if necessary.
The present invention will be explained more specifically with reference to the following examples. However the scope of the present invention is not limited to the following examples. In the present examples, when 1 is selected as m, and the carboxy group is selected as Y′ of the compound represented by the formula (I), the compounds are prepared, in which each of the partial structures including E and the substituent groups is selected from those shown in the Tables 1-1 to 1-27. Furthermore, when 1 is selected as m and the 1H-tetrazol-5-yl group is selected as Y in the compound represented by the formula (I), the compounds wherein each of the partial structures including E and the substituent groups shown on the Table 2 is respectively selected as the partial structure and the groups are prepared. Furthermore, when 0 is selected as m of the compound represented by the formula (I), the compounds wherein each of the partial structures, the groups and numeric values shown on the Tables 3-1 to 3-12 is respectively selected as the partial structure including E, the substituent groups and j are prepared.
In the following, the number and the structure formula of the intermediate prepared in each example are shown, respectively.
A mixture of 2-benzyloxyphenylacetic acid (242 mg, 1.0 mmol), N-bromosuccinimide (178 mg, 1.9 mmol) and dichloromethane (4 ml) was stirred overnight at room temperature under argon atmosphere. The reaction mixture was diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (280 mg, 87.2%) as a white solid.
1H-NMR (CDCl3) δ: 3.67 (2H, s), 5.04 (2H, s), 6.78 (1H, d, J=9.6 Hz), 7.25-7.37 (7H, m).
A mixture of the intermediate 1(1) (261 mg, 0.813 mmol), 4-(trifluoromethoxy)phenylboronic acid (218 mg, 1.056 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (43 mg, 0.057 mmol), potassium carbonate (169 mg, 1.22 mmol), dioxane (4 ml) and water (0.5 ml) was stirred at 80° C. for 2 hours. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, and the solution was filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:2) to give the title compound (160 mg, 48.9%) as a white solid.
1H-NMR (CDCl3) δ: 3.78 (2H, s), 5.11 (2H, s), 6.99 (1H, d, J=8.1 Hz), 7.23-7.45 (9H, m), 7.53 (2H, d, J=9.0 Hz).
A mixture of benzyl bromide (2.04 g, 11.926 mmol), 5-bromosalicylaldehyde (1.844 g, 9.174 mmol), potassium carbonate (5.07 g, 36.696 mmol) and dimethylformamide (15 ml) was stirred at 50° C. for 2 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with methanol to give the title compound (1.2 g, 44.9%) as a white solid.
1H-NMR (CDCl3) δ: 5.10 (2H, s), 6.80 (1H, d, J=9.0 Hz), 7.28-7.44 (6H, m), 7.69 (1H, d, J=2.4 Hz), 10.46 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 2(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 63.0% (pale yellow solid).
1H-NMR (DMSO-d6) δ: 5.37 (2H, s), 7.32-7.57 (8H, m), 7.75-7.85 (2H, m), 7.96-8.03 (2H, m), 10.47 (1H, s).
A mixture of the intermediate 2(2) (4.0 g, 9.336 mmol), malonic acid (2.137 g, 20.539 mmol), pyridine (4.3 ml) and piperidine (184 μl, 1.867 mmol) was refluxed for 1 hour under argon atmosphere. The reaction mixture was cooled to room temperature, adjusted to pH 1 by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (4.26 g, 97.0%) as a white solid.
1H-NMR (DMSO-d6) δ: 5.24 (2H, s), 6.63 (1H, d, J=16.2 Hz), 7.04 (1H, d, J=8.7 Hz), 7.23-7.58 (10H, m), 7.73 (1H, d, J=6.9 Hz), 8.20 (1H, d, J=16.2 Hz).
A mixture of the compound 2 (100 mg, 0.241 mmol), platinum oxide (5 mg) and ethanol (10 ml) was stirred for 1 hour under hydrogen atmosphere. The reaction mixture was filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was washed with methanol under suspension to give the title compound (78 mg, 78.0%) as a white solid.
1H-NMR (CDCl3) δ: 2.74 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.8 Hz), 5.14 (2H, s), 6.96 (2H, d, J=8.4 Hz), 7.22-7.54 (11H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-(tert-butyl)benzyl bromide and 5-bromosalicylaldehyde; Yield: 42.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 5.14 (2H, s), 6.97 (1H, d, J=8.7 Hz), 7.35 (2H, d, J=8.7 Hz), 7.43 (2H, d, J=8.7 Hz), 7.60 (1H, dd, J=2.7, 8.7 Hz), 7.94 (1H, d, J=2.7 Hz), 10.45 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 4(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 47.2% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.21 (2H, s), 7.16 (1H, d, J=9.0 Hz), 7.24-7.29 (2H, m), 7.37-7.47 (4H, m), 7.56-7.60 (2H, m), 7.73 (1H, dd, J=2.4, 9.0 Hz), 8.06 (1H, d, J=2.4 Hz), 10.59 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 4(2) and malonic acid; Yield: 49.1% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 5.20 (2H, s), 6.63 (1H, d, J=16.2 Hz), 7.07 (1H, d, J=8.4 Hz), 7.23-7.57 (10H, m), 7.74 (1H, d, J=2.1 Hz), 8.20 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 4; Yield: 54.8% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.74 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 5.11 (2H, s), 6.97 (1H, d, J=8.1 Hz), 7.22-7.25 (2H, m), 7.35-7.44 (5H, m), 7.53 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-(tert-butyl)benzyl bromide and 4-bromo-2-nitrophenol; Yield: 77.1% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.19 (2H, s), 7.02 (1H, d, J=8.7 Hz), 7.34-7.43 (4H, m), 7.58 (1H, dd, J=2.7, 8.7 Hz), 7.97 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 6(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 74.6% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.26 (2H, s), 7.22 (1H, d, J=8.7 Hz), 7.28-7.58 (8H, m), 7.68 (1H, dd, J=2.4, 8.7 Hz), 8.05 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 6(2); Yield: 83.5% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.93 (2H, brs), 5.09 (2H, s), 6.87-6.97 (3H, m), 7.22-7.57 (8H, m).
A solution of methyl chloroglyoxylate (184 μl, 2.0 mmol) in dichloromethane (1.5 ml) was added dropwise at a slow speed to a mixture of the intermediate 6(3) (415 mg, 1.0 mmol), sodium hydrogen carbonate (168 mg, 2.0 mmol), water (5 ml) and dichloromethane (7 ml), and the mixture was stirred at 0° C. for 2 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (456 mg, 90.9%) as a white solid.
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.97 (3H, s), 5.20 (2H, s), 7.07 (1H, d, J=8.4 Hz), 7.22-7.62 (9H, m), 8.70 (1H, d, J=2.4 Hz), 9.62 (1H, brs).
A mixture of the intermediate 6(4) (436 mg, 0.869 mmol), methanol (2 ml), tetrahydrofuran (2 ml) and a 2 N aqueous solution of sodium hydroxide (1.3 ml) was stirred at room temperature for 30 minutes. The precipitated solid was collected by filtration, and washed with methanol to give the title compound (390 mg, 88.1%) as a white solid.
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 5.25 (2H, s), 7.26 (1H, s), 7.26 (1H, d, J=8.4 Hz), 7.34 (1H, dd, J=2.4, 8.4 Hz), 7.67 (1H, d, J=8.7 Hz), 8.68 (2H, d, J=2.4 Hz), 10.38 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 2(1) and 2-nitrophenylboronic acid; Yield: 29.1% (pale yellow solid).
1H-NMR (CDCl3) δ: 5.17 (2H, s), 6.99 (1H, d, J=8.7 Hz), 7.24 (1H, dd, J=8.7, 2.1 Hz), 7.30-7.51 (7H, m), 7.53-7.61 (2H, m), 7.82 (1H, dd, J=8.7, 1.2 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 7(1) and malonic acid; Yield: 42.4% (yellow solid).
1H-NMR (DMSO-d6) δ: 5.27 (2H, s), 6.59 (1H, d, J=16.2 Hz), 7.26 (1H, d, J=8.4 Hz), 7.32-7.52 (6H, m), 7.59-7.64 (2H, m), 7.72-7.78 (2H, m), 7.86 (1H, d, J=16.2 Hz), 7.96-8.00 (1H, m), 12.36 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 7; Yield: 39.1% (pink solid).
1H-NMR (DMSO-d6) δ: 2.56 (2H, t, J=7.8 Hz), 2.87 (2H, t, J=7.8 Hz), 4.71 (2H, brs), 5.17 (2H, s), 6.55-6.63 (1H, m), 6.73 (1H, d, J=8.4 Hz), 6.93-7.03 (2H, m), 7.10 (1H, d, J=8.4 Hz), 7.19-7.23 (2H, m), 7.31-7.36 (1H, m), 7.39-7.44 (2H, m), 7.48-7.50 (2H, m), 12.08 (1H, brs).
A mixture of 4-(tert-butyl)benzyl bromide (2.240 g, 9.861 mmol), 2-hydroxyphenylacetic acid (1.00 g, 6.572 mmol), potassium carbonate (3.996 g, 28.918 mmol), chloroform (6 ml) and methanol (6 ml) was refluxed for 2 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1) to give the title compound (1.007 g, 51.4%) as a white solid.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.73 (2H, s), 5.06 (2H, s), 6.92-6.97 (2H, m), 7.21-7.41 (6H, m).
The title compound was obtained in the same manner as the Example 1(1) using the following starting material.
Starting material: the intermediate 9(1); Yield: 49.9% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.68 (3H, s), 5.02 (2H, s), 6.81 (2H, d, J=9.6 Hz), 7.26-7.39 (6H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 9(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 19.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 3.64 (2H, s), 5.14 (2H, s), 7.13 (1H, d, J=8.7 Hz), 7.36-7.43 (6H, m), 7.54-7.57 (2H, m), 7.72 (2H, d, J=8.1 Hz), 12.28 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 9(2) and 3,4-(methylenedioxy)phenylboronic acid; Yield: 30.3% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 3.62 (2H, s), 5.11 (2H, s), 6.04 (2H, s), 6.96 (2H, d, J=8.1 Hz), 7.05-7.09 (2H, m), 7.17 (2H, d, J=1.5 Hz), 7.35-7.48 (6H, m), 12.23 (1H, s).
The title compound was obtained in the same manner as the Example 9(1) using the following starting materials.
Starting materials: 2-hydroxyphenylacetic acid and 3,5-dimethylbenzyl bromide; Yield: 33.9% (white solid).
1H-NMR (CDCl3) δ: 2.29 (6H, s), 3.72 (2H, s), 5.00 (2H, s), 6.91-6.96 (3H, m), 7.00 (2H, s), 7.19-7.23 (1H, m), 7.24-7.28 (1H, m).
The title compound was obtained in the same manner as the Example 1(1) using the following starting material.
Starting material: the intermediate 11(1); Yield: 38.5% (white solid).
1H-NMR (CDCl3) δ: 2.29 (6H, s), 3.72 (2H, s), 5.00 (2H, s), 6.91-6.96 (3H, m), 7.00 (2H, s), 7.19-7.23 (1H, m), 7.24-7.28 (1H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 11(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 7.2% (white solid).
1H-NMR (CDCl3) δ: 2.30 (6H, s), 3.78 (2H, s), 5.05 (2H, s), 6.93-7.02 (4H, m), 7.23-7.27 (2H, m), 7.40-7.45 (2H, m), 7.53 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 5-bromo-2-fluorobenzaldehyde and 4-(trifluoromethoxy)phenylboronic acid; Yield: 91.6% (pale yellow oil).
1H-NMR (CDCl3) δ: 7.24-7.33 (3H, m), 7.55-7.61 (2H, m), 7.76-7.82 (1H, m), 8.05 (1H, dd, J=2.4, 6.3 Hz), 10.42 (1H, s).
A mixture of the intermediate 12(1) (750 mg, 2.639 mmol), 4-(tert-butyl)phenol (436 mg, 2.903 mmol), potassium carbonate (547 mg, 3.958 mmol) and dimethylacetamide (4 ml) was stirred at 160° C. for 1 hour. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15:1) to give the title compound (598 mg, 54.7%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 1.35 (9H, s), 1.27 (1H, d, J=8.7 Hz), 6.98 (2H, d, J=8.7 Hz), 7.28 (2H, d, J=8.4 Hz), 7.43 (2H, d, J=8.7 Hz), 7.59 (2H, d, J=8.4 Hz), 7.68 (1H, dd, J=2.7, 8.7 Hz), 8.12 (1H, d, J=2.7 Hz), 10.58 (1H, t, J=8.1 Hz).
A solution of potassium bis(trimethylsilyl)amide (414 mg, 1.973 mmol) in tetrahydrofuran (3 ml) was added dropwise at a slow speed to a mixture of bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate (627 mg, 1.973 mmol), 18-crown-6 (2.048 g, 7.750 mmol) and tetrahydrofuran (20 ml) at −78° C. under argon atmosphere. A solution of the intermediate 12(2) (584 mg, 1.409 mmol) in tetrahydrofuran (3 ml) was added dropwise at a slow speed to the mixture at −78° C. under argon atmosphere, and the mixture was stirred at −78° C. for 30 minutes. A saturated aqueous solution of ammonium chloride was added to the reaction mixture. The residue obtained by evaporation of the solvent under reduced pressure was diluted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15:1) to give the title compound (597 mg, 90.1%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.71 (3H, s), 6.04 (1H, d, J=12.6 Hz), 6.90-6.98 (3H, m), 7.20-7.31 (3H, m), 7.36 (2H, d, J=9.6 Hz), 7.44 (1H, dd, J=2.4, 8.4 Hz), 7.59 (2H, d, J=8.7 Hz), 7.95 (1H, d, J=2.4 Hz).
A mixture of the intermediate 12(3) (590 mg, 1.293 mmol), methanol (1 ml), tetrahydrofuran (4 ml) and a 2 N aqueous solution of sodium hydroxide (1.94 ml) was stirred at 60° C. for 1 hour. The reaction mixture was cooled to room temperature, acidified by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (550 mg, 93.2%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.49 (2H, s), 6.06 (1H, d, J=12.6 Hz), 6.91 (1H, d, J=8.4 Hz), 6.95 (2H, d, J=8.7 Hz), 7.20-7.24 (2H, m), 7.30-7.36 (3H, m), 7.43 (1H, dd, J=2.1, 8.4 Hz), 7.50-7.54 (2H, m), 7.90 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 12; Yield: 75.4% (clear colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.76 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 6.89 (1H, d, J=6.9 Hz), 6.93 (2H, d, J=8.7 Hz), 7.24-7.39 (5H, m), 7.46 (1H, d, J=2.1 Hz), 7.55 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and methyl 4-hydroxybenzoate; Yield: 40.5% (pale yellow solid).
1H-NMR (CDCl3) δ: 3.93 (3H, s), 7.09 (1H, d, J=8.7 Hz), 7.12 (2H, d, J=8.4 Hz), 7.32 (2H, d, J=8.4 Hz), 7.62 (2H, d, J=8.4 Hz), 7.77 (1H, dd, J=2.4, 8.7 Hz), 8.10 (2H, d, J=8.4 Hz), 8.16 (1H, d, J=2.4 Hz), 10.47 (1H, s).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 14(1) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate; Yield: 84.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.69 (3H, s), 3.90 (3H, s), 5.01 (1H, d, J=12.3 Hz), 6.99 (2H, d, J=9.3 Hz), 7.06 (1H, d, J=8.7 Hz), 7.09 (1H, d, J=12.3 Hz), 7.29 (2H, d, J=8.4 Hz), 7.54 (1H, dd, J=2.4, 8.7 Hz), 7.61 (2H, d, J=8.4 Hz), 7.92 (1H, d, J=2.4 Hz), 8.00 (2H, d, J=9.3 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 14(2); Yield: 58.5% (white solid).
1H-NMR (DMSO-d6) δ: 6.05 (1H, d, J=12.6 Hz), 6.97-7.06 (3H, m), 7.15 (1H, d, J=9.0 Hz), 7.45-7.50 (2H, m), 7.71 (1H, dd, J=2.1, 9.0 Hz), 7.78 (2H, d, J=8.7 Hz), 7.92-7.97 (3H, m), 12.69 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 14(3); Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 2.57 (2H, t, J=7.5 Hz), 2.85 (2H, t, J=7.5 Hz), 7.03 (2H, d, J=8.7 Hz), 7.10 (1H, d, J=8.4 Hz), 7.46 (2H, d, J=8.7 Hz), 7.60 (1H, dd, J=2.4, 8.4 Hz), 7.72 (1H, d, J=2.4 Hz), 7.81 (2H, d, J=8.7 Hz), 7.96 (2H, d, J=8.7 Hz).
A mixture of 5-bromo-2-fluorobenzaldehyde (1.07 g, 5.280 mmol), 4-(trifluoromethoxy)phenol (940 mg, 5.280 mmol), potassium carbonate (1.46 g, 10.560 mmol), copper(II) oxide (420 mg, 5.280 mmol) and pyridine (10 ml) was stirred at 180° C. for 6 hours. The reaction mixture was cooled to room temperature and filtered through Celite. The filtrate was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (1.58 g, 83.1%) as a brown oil.
1H-NMR (CDCl3) δ: 6.18 (1H, d, J=8.7 Hz), 7.09 (2H, d, J=8.7 Hz), 7.25-7.28 (2H, m), 7.61-7.65 (1H, m), 8.05 (1H, d, J=2.4 Hz), 10.41 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 15(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 94.3% (clear yellow oil).
1H-NMR (CDCl3) δ: 7.00 (1H, d, J=8.4 Hz), 7.12-7.15 (2H, m), 7.26-7.32 (4H, m), 7.59-7.62 (2H, m), 7.73 (1H, dd, J=8.4, 2.4 Hz), 8.15 (1H, d, J=2.4 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 15(2) and malonic acid; Yield: 64.5% (white solid).
1H-NMR (CDCl3) δ: 6.64 (1H, d, J=16.2 Hz), 6.96 (1H, d, J=8.7 Hz), 7.05-7.08 (2H, m), 7.23-7.33 (4H, m), 7.53 (1H, dd, J=8.7, 2.4 Hz), 7.57-7.60 (2H, m), 7.82 (1H, d, J=2.4 Hz), 8.12 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 15; Yield: 87.8% (clear colorless oil).
1H-NMR (CDCl3) δ: 2.74 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 6.92 (1H, d, J=8.7 Hz), 6.98-7.02 (2H, m), 7.20 (2H, d, J=8.1 Hz), 7.26-7.29 (2H, m), 7.38 (1H, dd, J=8.7, 2.1 Hz), 7.48 (1H, d, J=2.1 Hz), 7.53-7.58 (2H, m).
A mixture of the intermediate 6(4) (3.0 g, 5.982 mmol), methyl iodide (9.387 g, 66.180 mmol), potassium carbonate (2.480 g, 17.946 mmol), 18-crown-6 (158 mg, 0.598 mmol) and acetonitrile (50 ml) was stirred at 85° C. for 3 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (3.066 g, 99.4%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.12 (3H, s), 3.55 (3H, s), 5.15 (2H, s), 7.08 (1H, d, J=8.4 Hz), 7.24-7.29 (2H, m), 7.34-7.53 (8H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 17(1); Yield: 90.1% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 3.18 (3H, s), 5.13-5.26 (2H, m), 7.28 (2H, d, J=8.7 Hz), 7.39-7.46 (6H, m), 7.62 (1H, d, J=2.1 Hz), 7.69 (1H, dd, J=2.1, 8.7 Hz), 7.73 (2H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 5-bromosalicylaldehyde and 4-(trifluoromethoxy)phenylboronic acid; Yield: 78.1% (yellow solid).
1H-NMR (CDCl3) δ: 7.09 (1H, d, J=8.1 Hz), 7.30 (2H, d, J=7.8 Hz), 7.54-7.59 (2H, m), 7.72-7.76 (2H, m), 9.98 (1H, s), 11.03 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-chlorobenzyl chloride; Yield: 73.1% (white solid).
1H-NMR (CDCl3) δ: 5.22 (2H, s), 7.11 (1H, d, J=8.7 Hz), 7.26-7.29 (2H, m), 7.39-7.41 (4H, m), 7.56-7.59 (2H, m), 7.74 (1H, dd, J=8.7, 2.4 Hz), 8.07 (1H, d, J=2.4 Hz), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 18(2) and malonic acid; Yield: 84.2% (white solid).
1H-NMR (CDCl3) δ: 5.20 (2H, s), 6.62 (1H, d, J=16.2 Hz), 7.01 (1H, d, J=8.4 Hz), 7.29 (2H, d, J=8.7 Hz), 7.38-7.39 (4H, m), 7.50-7.57 (3H, m), 7.74 (1H, d, J=2.4 Hz), 8.18 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 18; Yield: 50.0% (white solid).
1H-NMR (CDCl3) δ: 2.72 (2H, t, J=7.2 Hz), 3.05 (2H, t, J=7.2 Hz), 5.10 (2H, s), 6.93 (1H, d, J=8.4 Hz), 7.22-7.26 (2H, m), 7.35-7.40 (6H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-fluorobenzyl chloride; Yield: 96.8% (brown solid).
1H-NMR (CDCl3) δ: 5.21 (2H, s), 7.09-7.15 (3H, m), 7.26-7.30 (2H, m), 7.42-7.47 (2H, m), 7.56-7.59 (2H, m), 7.75 (1H, dd, J=8.7, 2.4 Hz), 8.07 (1H, d, J=2.4 Hz), 10.57 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 20(1) and malonic acid; Yield: 62.5% (white solid).
1H-NMR (CDCl3) δ: 5.19 (2H, s), 6.61 (1H, d, J=16.2 Hz), 7.03 (1H, d, J=8.7 Hz), 7.07-7.15 (2H, m), 7.29 (2H, d, J=8.4 Hz), 7.41-7.46 (2H, m), 7.51-7.57 (3H, m), 7.74 (1H, d, J=2.1 Hz), 8.18 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 20(2); Yield: 55.9% (white solid).
1H-NMR (CDCl3) δ: 2.72 (2H, t, J=7.5 Hz), 3.05 (2H, t, J=7.5 Hz), 5.10 (2H, s), 6.96 (1H, d, J=8.4 Hz), 7.01 (2H, t, J=8.7 Hz), 7.25 (2H, d, J=8.1 Hz), 7.36-7.44 (4H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 2-(trifluoromethyl)benzyl chloride; Yield: 72.9% (pale pink solid).
1H-NMR (CDCl3) δ: 5.45 (2H, s), 7.11 (1H, d, J=8.7 Hz), 7.29 (2H, d, J=8.7 Hz), 7.49 (1H, t, J=7.2 Hz), 7.56-7.65 (3H, m), 7.73-7.77 (3H, m), 8.09 (1H, d, J=2.4 Hz), 10.62 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 21(1) and malonic acid; Yield: 89.7% (white solid).
1H-NMR (CDCl3) δ: 5.43 (2H, s), 6.63 (1H, d, J=16.2 Hz), 6.98 (1H, d, J=8.4 Hz), 7.29 (2H, d, J=8.1 Hz), 7.44-7.63 (5H, m), 7.71-7.77 (3H, m), 8.25 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 21(2); Yield: 79.1% (white solid).
1H-NMR (CDCl3) δ: 2.76 (2H, t, J=7.5 Hz), 3.10 (2H, t, J=7.5 Hz), 5.34 (2H, s), 6.92 (1H, d, J=8.4 Hz), 7.25 (2H, t, J=7.8 Hz), 7.37 (1H, dd, J=8.4, 2.4 Hz), 7.41 (1H, d, J=2.4 Hz), 7.44 (1H, d, J=7.8 Hz), 7.50-7.61 (3H, m), 7.70-7.75 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-(trifluoromethyl)benzyl chloride; Yield: 100.0% (clear brown oil).
1H-NMR (CDCl3) δ: 5.32 (2H, s), 7.11 (1H, d, J=8.7 Hz), 7.29 (2H, d, J=8.7 Hz), 7.65-7.61 (4H, m), 7.70 (2H, d, J=8.4 Hz), 7.75 (1H, dd, J=8.7, 2.7 Hz), 8.09 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 22(1) and malonic acid; Yield: 53.4% (white solid).
1H-NMR (CDCl3) δ: 5.29 (2H, s), 6.63 (1H, d, J=16.2 Hz), 7.00 (1H, d, J=8.7 Hz), 7.29 (2H, d, J=8.1 Hz), 7.51-7.59 (5H, m), 7.69 (2H, d, J=8.7 Hz), 7.76 (1H, d, J=2.1 Hz), 8.21 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 22(2); Yield: 67.3% (white solid).
1H-NMR (CDCl3) δ: 2.74 (2H, t, J=7.5 Hz), 3.08 (2H, t, J=7.5 Hz), 5.19 (2H, s), 6.92 (1H, d, J=8.1 Hz), 7.23-7.26 (2H, m), 7.35-7.41 (2H, m), 7.50-7.57 (4H, m), 7.66 (2H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 2-methoxybenzyl chloride; Yield: 77.0% (white solid).
1H-NMR (CDCl3) δ: 3.89 (3H, s), 5.29 (2H, s), 6.95 (1H, d, J=8.4 Hz), 6.98-7.03 (1H, m), 7.19 (1H, d, J=8.4 Hz), 7.26-7.29 (2H, m), 7.32-7.38 (1H, m), 7.45-7.48 (1H, m), 7.56-7.61 (2H, m), 7.74 (1H, dd, J=8.4 Hz, J=2.4 Hz), 8.06 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 23(1) and malonic acid; Yield: 65.4% (white solid).
1H-NMR (CDCl3) δ: 3.90 (3H, s), 5.28 (2H, s), 6.65 (1H, d, J=16.2 Hz), 6.94 (1H, d, J=8.1 Hz), 6.97-7.02 (1H, m), 7.09 (1H, d, J=8.7 Hz), 7.26-7.36 (3H, m), 7.44 (1H, dd, J=8.1, 1.5 Hz), 7.50-7.57 (3H, m), 7.72 (1H, d, J=2.1 Hz), 8.21 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 23(2); Yield: 74.8% (white solid).
1H-NMR (CDCl3) δ: 2.76 (2H, t, J=7.2 Hz), 3.06 (2H, t, J=7.2 Hz), 3.87 (3H, s), 5.17 (2H, s), 6.91-7.03 (3H, m), 7.23-7.57 (8H, m).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 2(2) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate; Yield: 66.1% (clear colorless oil).
1H-NMR (CDCl3) δ: 3.68 (3H, s), 5.14 (2H, s), 7.01 (1H, d, J=8.7 Hz), 7.24-7.50 (9H, m), 7.54-7.59 (3H, m), 7.91 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 24(1); Yield: 55.3% (white solid).
1H-NMR (CDCl3) δ: 5.14 (2H, s), 6.04 (1H, d, J=12.9 Hz), 7.01 (1H, d, J=8.7 Hz), 7.19 (2H, d, J=8.1 Hz), 7.32-7.51 (9H, m), 7.86 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 4(2) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate; Yield: 64.2% (white solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 3.69 (3H, s), 5.11 (2H, s), 7.02 (1H, d, J=8.4 Hz), 7.23-7.45 (7H, m), 7.49 (1H, dd, J=2.4, 8.4 Hz), 7.54-7.60 (2H, m), 7.92 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 25(1); Yield: 83.4% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.10 (2H, s), 6.02 (1H, d, J=12.3 Hz), 7.01 (1H, d, J=8.7 Hz), 7.17 (2H, d, J=8.7 Hz), 7.34-7.50 (8H, m), 7.87 (1H, d, J=2.4 Hz).
A solution of triethyl phosphonoacetate (1.356 g, 6.048 mmol) in tetrahydrofuran (45 ml) was added dropwise at a slow speed to sodium hydride (264 mg, 6.048 mmol) at room temperature under argon atmosphere, and the mixture was stirred at room temperature for 30 minutes. A solution of the intermediate 4(1) (1.5 g, 4.319 mmol) in tetrahydrofuran (25 ml) was added dropwise at a slow speed to the mixture at 0° C. under argon atmosphere, and the mixture was stirred at room temperature overnight. A small portion of saturated aqueous solution of ammonium chloride was added to the reaction mixture. The residue obtained by evaporation of tetrahydrofuran under reduced pressure was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (1.59 g, 88.2%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.24-1.43 (12H, m), 4.25 (2H, q, J=7.2 Hz), 5.10 (2H, s), 6.49 (1H, d, J=16.2 Hz), 6.84 (1H, d, J=8.7 Hz), 7.32-7.43 (5H, m), 7.63 (1H, d, J=2.7 Hz), 7.98 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 26(1) and 3-carboxyphenylboronic acid; Yield: 49.3% (white solid).
1H-NMR (CDCl3) δ: 1.28-1.37 (12H, m), 4.27 (2H, q, J=7.2 Hz), 5.20 (2H, s), 6.63 (1H, d, J=16.2 Hz), 7.07 (1H, d, J=9.0 Hz), 7.36-7.45 (4H, m), 7.52-7.60 (2H, m), 7.78-7.82 (2H, m), 8.06-8.11 (1H, m), 8.14 (1H, d, J=16.2 Hz), 8.31 (1H, t, J=1.8 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 26(2); Yield: 86.5% (white solid).
1H-NMR (CDCl3) δ: 1.21-1.34 (12H, m), 2.70 (2H, d, J=7.5 Hz), 3.09 (2H, d, J=7.5 Hz), 4.13 (2H, q, J=7.2 Hz), 5.13 (2H, s), 7.10 (1H, d, J=8.4 Hz), 7.37-7.54 (7H, m), 7.76-7.81 (1H, m), 8.02-8.07 (1H, m), 8.30 (1H, t, J=1.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 26(3); Yield: 59.1% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.58 (2H, d, J=7.8 Hz), 2.91 (2H, d, J=7.8 Hz), 5.16 (2H, s), 7.15 (1H, d, J=9.0 Hz), 7.38-7.57 (7H, m), 7.83-7.89 (1H, m), 8.13 (1H, t, J=1.5 Hz), 12.58 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 2,4-dichlorobenzyl chloride; Yield: 78% (white solid).
1H-NMR (CDCl3) δ: 5.30 (2H, s), 7.13 (1H, d, J=8.7 Hz), 7.25-7.35 (3H, m), 7.47 (1H, d, J=2.1 Hz), 7.52 (1H, d, J=8.1 Hz), 7.55-7.61 (2H, m), 7.75 (1H, dd, J=2.7, 8.7 Hz), 8.08 (1H, d, J=2.7 Hz), 10.59 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 27(1) and malonic acid; Yield: 75% (white solid).
1H-NMR (CDCl3) δ: 5.28 (2H, s), 6.61 (1H, d, J=15.9 Hz), 7.00 (1H, d, J=8.4 Hz), 7.25-7.36 (3H, m), 7.46-7.58 (5H, m), 7.75 (1H, d, J=2.4 Hz), 8.21 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting materials.
Starting material: the intermediate 27(2); Yield: 30% (white solid).
1H-NMR (CDCl3) δ: 2.74 (2H, t, J=7.5 Hz), 3.08 (2H, t, J=7.5 Hz), 5.18 (2H, s), 6.94 (1H, d, J=8.4 Hz), 7.23-7.32 (3H, m), 7.36-7.45 (3H, m), 7.48-7.56 (3H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 3-methylbenzyl bromide; Yield: 50% (white solid).
1H-NMR (CDCl3) δ: δ 2.39 (3H, s), 5.21 (2H, s), 7.14 (1H, d, J=8.5 Hz), 7.18 (1H, d, J=7.0 Hz), 7.23-7.33 (5H, m), 7.55-7.60 (2H, m), 7.73 (1H, dd, J=8.5, 2.5 Hz), 8.06 (1H, d, J=2.5 Hz), 10.60 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 28(1) and malonic acid; Yield: 92% (white solid).
1H-NMR (DMSO-d6) δ: 2.33 (3H, s), 5.23 (2H, s), 6.74 (1H, d, J=16.0 Hz), 7.17 (1H, d, J=7.0 Hz), 7.25-7.34 (4H, m), 7.41-7.48 (2H, m), 7.72 (1H, dd, J=8.5, 2.0 Hz), 7.82-7.87 (2H, m), 7.91 (1H, d, J=16.0 Hz), 8.04 (1H, d, J=2.0 Hz), 12.37 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting materials.
Starting material: the intermediate 28(2); Yield: 66% (white solid).
1H-NMR (DMSO-d6) δ: 2.33 (3H, s), 2.57 (2H, t, J=8.0 Hz), 2.90 (2H, t, J=8.0 Hz), 5.15 (2H, s), 7.10-7.15 (2H, m), 7.25-7.32 (3H, m), 7.41 (2H, d, J=9.0 Hz), 7.47-7.51 (2H, m), 7.72 (2H, d, J=9.0 Hz), 12.13 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-phenylbenzyl bromide; Yield: 99% (white solid).
1H-NMR (DMSO-d6) δ: 5.29 (2H, s), 7.17 (1H, d, J=8.5 Hz), 7.28 (2H, d, J=8.5 Hz), 7.34-7.39 (2H, m), 7.43-7.48 (2H, m), 7.52-7.66 (7H, m), 7.75 (1H, dd, J=8.5, 2.5 Hz), 8.08 (1H, d, J=2.5 Hz), 10.62 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 29(1) and malonic acid; Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 5.33 (2H, s), 6.76 (1H, d, J=16.0 Hz), 7.29-7.50 (6H, m), 7.58 (2H, d, J=8.5 Hz), 7.68-7.74 (5H, m), 7.85 (2H, d, J=8.5 Hz), 7.95 (1H, d, J=16.0 Hz), 8.06 (1H, d, J=2.0 Hz), 12.37 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 29(2); Yield: 20% (white solid).
1H-NMR (DMSO-d6) δ: 2.59 (2H, t, J=8.0 Hz), 2.93 (2H, t, J=8.0 Hz), 5.25 (2H, s), 7.16 (1H, d, J=9.5 Hz), 7.34-7.52 (7H, m), 7.57 (2H, d, J=8.5 Hz), 7.67-7.74 (6H, m), 12.13 (1H, s).
Methanesulfonyl chloride (3.069 g, 26.791 mmol) was added to a solution of 4-butylbenzyl alcohol (4.000 g, 24.355 mmol) in dichloromethane (120 ml) at 0° C. under argon atmosphere. Then triethylamine (2.711 g, 26.791 mmol) was added dropwise at a slow speed to this mixture at 0° C., and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue was diluted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane) to give the title compound (3.64 g, 82%) as a colorless oil.
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.5 Hz), 1.35 (2H, sext, J=7.5 Hz), 1.52-1.64 (2H, m), 2.60 (2H, t, J=7.5 Hz), 4.57 (2H, s), 7.15-7.18 (2H, m), 7.25-7.30 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and the intermediate 30(1); Yield: 43% (yellowish-white solid).
1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=7.0 Hz), 1.30 (2H, sext, J=7.0 Hz), 1.55 (2H, quint, J=7.0 Hz), 2.58 (2H, t, J=7.0 Hz), 5.31 (2H, s), 7.23 (2H, d, J=8.0 Hz), 7.44 (5H, d, J=8.0 Hz), 7.79 (2H, d, J=8.0 Hz), 7.95-8.00 (2H, m), 10.45 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 30(2) and malonic acid; Yield: 58% (white solid).
1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=7.5 Hz), 1.31 (2H, sext, J=7.5 Hz), 1.51-1.61 (2H, m), 2.59 (2H, t, J=7.5 Hz), 5.23 (2H, s), 6.72 (1H, d, J=16.0 Hz), 7.23-7.29 (3H, m), 7.37-7.43 (4H, m), 7.72 (1H, dd, J=9.0, 2.0 Hz), 7.82-7.86 (2H, m), 7.90 (1H, d, J=16.0 Hz), 8.04 (1H, d, J=2.0 Hz), 12.34 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 30(3); Yield: 33% (white solid).
1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=7.5 Hz), 1.31 (2H, sext, J=7.5 Hz), 1.55 (2H, quint, J=7.5 Hz), 2.56 (2H, t, J=7.5 Hz), 2.58 (2H, t, J=7.5 Hz), 2.89 (2H, t, J=7.5 Hz), 5.15 (2H, s), 7.13 (1H, d, J=9.0 Hz), 7.21-7.23 (2H, m), 7.36-7.42 (4H, m), 7.47-7.50 (2H, m), 7.69-7.73 (2H, m), 12.12 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 4(1) and malonic acid; Yield: 84% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 5.17 (2H, s), 6.61 (1H, d, J=16.1 Hz), 7.13-7.17 (1H, m), 7.36-7.44 (4H, m), 7.52-7.55 (1H, m), 7.77 (1H, d, J=16.1 Hz), 7.90 (1H, s), 12.43 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and phenylboronic acid; Yield: 58% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.19 (2H, s), 6.63 (1H, d, J=16.1 Hz), 7.06 (1H, d, J=8.8 Hz), 7.33-7.46 (7H, m), 7.54-7.58 (3H, m), 7.78 (1H, d, J=2.4 Hz), 8.22 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 31; Yield: 33% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.74 (2H, t, J=7.6 Hz), 3.07 (2H, t, J=7.6 Hz), 5.11 (2H, s), 6.98 (1H, d, J=8.1 Hz), 7.29-7.44 (9H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-fluorophenylboronic acid; Yield: 52% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.20 (2H, s), 6.63 (1H, d, J=16.1 Hz), 7.04-7.15 (2H, m), 7.37-7.53 (8H, m), 7.72 (1H, d, J=2.2 Hz), 8.20 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material
Starting material: the compound 33; Yield: 22% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.74 (2H, t, J=7.6 Hz), 3.06 (2H, t, J=7.6 Hz), 5.10 (2H, s), 6.97 (1H, d, J=8.2 Hz), 7.08 (2H, t, J=8.6 Hz), 7.33-7.49 (8H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-(trifluoromethyl)phenylboronic acid; Yield: 49% (pale orange solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.21 (2H, s), 6.64 (1H, d, J=16.0 Hz), 7.09 (1H, d, J=8.6 Hz), 7.37-7.46 (4H, m), 7.57 (1H, dd, J=2.2, 8.6 Hz), 7.63-7.71 (4H, m), 7.77 (1H, d, J=2.2 Hz), 8.21 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 35; Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, m), 2.75 (2H, t, J=7.6 Hz), 3.07 (2H, t, J=7.6 Hz), 5.12 (2H, s), 7.01 (1H, d, J=8.2 Hz), 7.35-7.44 (6H, m), 7.60-7.67 (4H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-methoxyphenylboronic acid; Yield: 43% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.85 (3H, s), 5.18 (2H, s), 6.62 (1H, d, J=16.1 Hz), 6.96-7.05 (3H, m), 7.37-7.53 (7H, m), 7.73 (1H, d, J=2.2 Hz), 8.22 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 37; Yield: 74% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.51 (2H, t, J=7.6 Hz), 2.89 (2H, t, J=7.6 Hz), 3.78 (3H, s), 5.13 (2H, s), 6.96-6.99 (2H, m), 7.06-7.09 (1H, d, J=8.2 Hz), 7.38-7.45 (6H, m), 7.51-7.54 (2H, m), 12.10 (1H, bs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-(tert-butyl)phenylboronic acid; Yield: 58% (pale orange solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 1.36 (9H, s), 5.18 (2H, s), 6.62 (1H, d, J=16.1 Hz), 7.05 (1H, d, J=8.6 Hz), 7.37-7.51 (8H, m), 7.58 (1H, dd, J=2.0, 8.6 Hz), 7.77 (1H, d, J=2.0 Hz), 8.21 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 39; Yield: 50% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 1.35 (9H, s), 2.72-2.77 (2H, m), 3.04-3.09 (2H, m), 5.10 (2H, s), 6.97 (1H, d, J=8.4 Hz), 7.36-7.49 (10H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-methylphenylboronic acid; Yield: 51% (yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.39 (3H, s), 5.18 (2H, s), 6.62 (1H, d, J=16.1 Hz), 7.04 (1H, d, J=8.6 Hz), 7.23-7.26 (2H, m), 7.37-7.46 (6H, m), 7.54 (1H, dd, J=2.2, 8.6 Hz), 7.76 (1H, d, J=2.2 Hz), 8.21 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 41; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.37 (3H, s), 2.72-2.77 (2H, m), 3.04-3.09 (2H, m), 5.10 (2H, s), 6.97 (1H, d, J=8.2 Hz), 7.19-7.26 (2H, m), 7.36-7.45 (8H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-butylphenylboronic acid; Yield: 49% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.3 Hz), 1.30-1.42 (11H, m), 1.63 (2H, quint, J=7.8 Hz), 2.65 (2H, t, J=7.8 Hz), 5.18 (2H, s), 6.62 (1H, d, J=16.1 Hz), 7.04 (1H, d, J=8.8 Hz), 7.23-7.26 (3H, m), 7.37-7.47 (5H, m), 7.55 (1H, dd, J=2.4, 8.8 Hz), 7.76 (1H, d, J=2.4 Hz), 8.21 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 43(1); Yield: 49% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.3 Hz), 1.31-1.41 (11H, m), 1.62 (2H, quint, J=7.6 Hz), 2.63 (2H, t, J=7.7 Hz), 2.74 (2H, t, J=7.7 Hz), 3.06 (2H, t, J=7.6 Hz), 5.10 (2H, s), 6.97 (1H, d, J=8.2 Hz), 7.20-7.25 (2H, m), 7.35-7.46 (8H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-(methylsulfanyl)phenylboronic acid; Yield: 38% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.52 (3H, s), 5.19 (2H, s), 6.63 (1H, d, J=16.1 Hz), 7.05 (1H, d, J=8.8 Hz), 7.31-7.49 (8H, m), 7.53 (1H, dd, J=2.4, 8.8 Hz), 7.75 (1H, d, J=2.4 Hz), 8.21 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 2(1) and malonic acid; Yield: 44% (white solid).
1H-NMR (DMSO-d6) δ: 5.21 (2H, s), 6.61 (1H, d, J=16.0 Hz), 7.15 (1H, d, J=8.5 Hz), 7.32-7.47 (5H, m), 7.54 (1H, dd, J=8.5, 2.5 Hz), 7.77 (1H, d, J=16.0 Hz), 7.91 (1H, d, J=2.5 Hz), 12.42 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 45(1) and phenylboronic acid; Yield: 31% (yellow solid).
1H-NMR (DMSO-d6) δ: 5.27 (2H, s), 6.71 (1H, d, J=16.0 Hz), 7.27 (1H, d, J=8.5 Hz), 7.30-7.50 (8H, m), 7.68-7.72 (2H, m), 7.76-7.78 (1H, m), 7.91 (1H, d, J=16.0 Hz), 7.99-8.02 (1H, m), 12.33 (1H, s).
The title compound was obtained in the same manner as the Example 26(1) using the following starting materials.
Starting materials: 5-bromosalicylaldehyde and triethyl phosphonoacetate; Yield: 47% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.35 (3H, t, J=7.0 Hz), 4.30 (2H, q, J=7.0 Hz), 6.64 (1H, d, J=16.0 Hz), 6.78 (1H, d, J=8.5 Hz), 7.31 (1H, dd, J=8.5, 2.5 Hz), 7.36 (1H, brs), 7.58 (1H, d, J=2.5 Hz), 7.98 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 46(1) and phenylboronic acid; Yield: 44% (white solid).
1H-NMR (CDCl3) δ: 1.36 (3H, t, J=7.0 Hz), 4.31 (2H, q, J=7.0 Hz), 6.45 (1H, s), 6.71 (1H, d, J=16.0 Hz), 6.93 (1H, d, J=8.0 Hz), 7.31-7.35 (1H, m), 7.39-7.44 (2H, m), 7.47 (1H, dd, J=8.0, 2.5 Hz), 7.52-7.55 (2H, m), 7.69 (1H, d, J=2.5 Hz), 8.08 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 46(2); Yield: 99% (colorless oil).
1H-NMR (DMSO-d6) δ: 1.14 (3H, t, J=7.0 Hz), 2.60 (2H, t, J=7.5 Hz), 2.84 (2H, t, J=7.5 Hz), 4.04 (2H, q, J=7.0 Hz), 6.87 (1H, d, J=8.5 Hz), 7.26 (1H, tt, J=7.0, 2.0 Hz), 7.32 (1H, dd, J=8.5, 2.0 Hz), 7.37 (1H, d, J=2.0 Hz), 7.39-7.42 (2H, m), 7.53-7.57 (2H, m), 9.57 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 46(3) and benzyl bromide; Yield: 99% (white solid).
1H-NMR (DMSO-d6) δ: 1.13 (3H, t, J=7.0 Hz), 2.64 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 4.03 (2H, q, J=7.0 Hz), 5.19 (2H, s), 7.12 (1H, d, J=9.0 Hz), 7.27-7.48 (10H, m), 7.60 (2H, d, J=7.5 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 46(4); Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 2.58 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 5.19 (2H, s), 7.11 (1H, d, J=8.0 Hz), 7.27-7.48 (10H, m), 7.60 (2H, d, J=8.0 Hz), 12.12 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 45(1) and 4-(tert-butyl)phenylboronic acid; Yield: 40% (yellow solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 5.24 (2H, s), 6.64 (1H, d, J=16.0 Hz), 7.22 (1H, d, J=9.0 Hz), 7.34-7.49 (7H, m), 7.59-7.61 (3H, m), 7.80 (1H, d, J=16.0 Hz), 7.89-7.90 (1H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 47; Yield: 18% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 2.56 (2H, t, J=7.5 Hz), 2.90 (2H, t, J=7.5 Hz), 5.22 (2H, s), 7.09 (1H, d, J=9.0 Hz), 7.40-7.46 (6H, m), 7.52 (2H, d, J=9.0 Hz), 7.62 (2H, d, J=9.0 Hz), 12.14 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 4-chlorophenylboronic acid; Yield: 29% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.19 (2H, s), 6.63 (1H, d, J=16.1 Hz), 7.05 (1H, d, J=8.6 Hz), 7.36-7.49 (8H, m), 7.51 (1H, dd, J=2.2, 8.6 Hz), 7.73 (1H, d, J=2.2 Hz), 8.20 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 49; Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.74 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 5.11 (2H, s), 6.97 (1H, d, J=8.2 Hz), 7.34-7.47 (10H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-(trifluoromethoxy)benzyl bromide and 5-bromosalicylaldehyde; Yield: 66% (white solid).
1H-NMR (DMSO-d6) δ: 5.34 (2H, s), 7.32 (1H, d, J=9.0 Hz), 7.39-7.42 (2H, m), 7.66 (2H, d, J=8.5 Hz), 7.78 (1H, d, J=2.5 Hz), 7.84 (1H, dd, J=9.0, 2.5 Hz), 10.33 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 51(1) and malonic acid; Yield: 92% (white solid).
1H-NMR (DMSO-d6) δ: 5.26 (2H, s), 6.61 (1H, d, J=16.0 Hz), 7.14 (1H, d, J=9.0 Hz), 7.40-7.43 (2H, m), 7.55 (1H, dd, J=9.0, 2.5 Hz), 7.57-7.60 (2H, m), 7.77 (1H, d, J=16.0 Hz), 7.92 (1H, d, J=2.5 Hz), 12.43 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 51(2) and 4-(tert-butyl)phenylboronic acid; Yield: 35% (white solid).
1H-NMR (DMSO-d6) δ: 1.31 (9H, s), 5.31 (2H, s), 6.69 (1H, d, J=16.0 Hz), 7.24 (1H, d, J=8.5 Hz), 7.42-7.46 (4H, m), 7.61-7.64 (4H, m), 7.67 (1H, dd, J=8.5, 2.0 Hz), 7.91 (1H, d, J=16.0 Hz), 7.97 (1H, d, J=2.0 Hz), 12.36 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 51; Yield: 47% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 2.56 (2H, t, J=7.5 Hz), 2.90 (2H, t, J=7.5 Hz), 5.22 (2H, s), 7.09 (1H, d, J=9.0 Hz), 7.40-7.46 (6H, m), 7.52 (2H, d, J=9.0 Hz), 7.62 (2H, d, J=9.0 Hz), 12.14 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 51(2) and phenylboronic acid; Yield: 46% (white solid).
1H-NMR (CDCl3) δ: 5.21 (2H, s), 6.62 (1H, d, J=16.0 Hz), 7.02 (1H, d, J=8.5 Hz), 7.27 (2H, d, J=8.0 Hz), 7.34 (1H, tt, J=8.0, 1.5 Hz), 7.42-7.50 (4H, m), 7.56 (2H, d, J=8.5 Hz), 7.57 (1H, dd, J=8.5, 2.5 Hz), 7.79 (1H, d, J=2.5 Hz), 8.20 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 53(1); Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 2.73 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 5.13 (2H, s), 6.95 (1H, d, J=8.0 Hz), 7.23-7.25 (2H, m), 7.27-7.33 (1H, m), 7.38-7.55 (8H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 46(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 37% (yellow solid).
1H-NMR (CDCl3) δ: 1.37 (3H, t, J=7.0 Hz), 4.32 (2H, q, J=7.0 Hz), 6.74 (1H, d, J=16.0 Hz), 6.95 (1H, d, J=8.5 Hz), 6.98 (1H, s), 7.26 (2H, d, J=8.0 Hz), 7.43 (1H, dd, J=2.0, 8.5 Hz), 7.52-7.55 (2H, m), 7.65 (1H, d, J=2.0 Hz), 8.09 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting materials: the intermediate 54(1); Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.0 Hz), 2.76 (2H, t, J=6.0 Hz), 2.95 (2H, t, J=6.0 Hz), 4.16 (2H, q, J=7.0 Hz), 6.97 (1H, d, J=8.5 Hz), 7.24 (2H, d, J=9.0 Hz), 7.28 (1H, d, J=2.5 Hz), 7.32 (1H, dd, J=2.5, 8.5 Hz), 7.47 (1H, s), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 54(2) and 4-nitrobenzyl bromide; Yield: 66% (white solid).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.0 Hz), 2.69 (2H, t, J=7.5 Hz), 3.09 (2H, t, J=7.5 Hz), 4.13 (2H, q, J=7.0 Hz), 5.25 (2H, s), 6.91 (1H, d, J=8.5 Hz), 7.26 (2H, d, J=8.0 Hz), 7.37 (1H, dd, J=8.5, 2.5 Hz), 7.42 (1H, d, J=2.5 Hz), 7.52-7.55 (2H, m), 7.64 (2H, d, J=8.5 Hz), 8.26-8.29 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 54(3); Yield: 42% (white solid).
1H-NMR (DMSO-d6) δ: 2.60 (2H, t, J=7.5 Hz), 2.95 (2H, t, J=7.5 Hz), 5.38 (2H, s), 7.11 (1H, d, J=8.5 Hz), 7.42 (2H, d, J=9.0 Hz), 7.50 (1H, dd, J=8.5, 2.0 Hz), 7.54 (1H, d, J=2.0 Hz), 7.71-7.77 (4H, m), 8.27-8.29 (2H, m), 12.14 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 2-methoxyphenylboronic acid; Yield: 54% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.82 (3H, s), 5.18 (2H, s), 6.58 (1H, d, J=16.1 Hz), 6.97-7.04 (3H, m), 7.28-7.32 (2H, m), 7.38-7.45 (4H, m), 7.51 (1H, dd, J=2.0, 8.4 Hz), 7.74 (1H, d, J=2.0 Hz), 8.21 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 55; Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, m), 2.74 (2H, t, J=7.8 Hz), 3.05 (2H, t, J=7.8 Hz), 3.80 (3H, s), 5.10 (2H, s), 6.94-7.03 (3H, m), 7.24-7.30 (2H, m), 7.34-7.44 (6H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 3-(trifluoromethyl)benzyl bromide; Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 5.29 (2H, s), 7.13 (1H, d, J=9.0 Hz), 7.29 (2H, d, J=8.5 Hz), 7.56-7.60 (2H, m), 7.63-7.73 (4H, m), 7.76 (1H, dd, J=9.0, 2.5 Hz), 8.09 (1H, d, J=2.5 Hz), 10.59 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 57(1) and malonic acid; Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 5.27 (2H, s), 6.62 (1H, d, J=16.0 Hz), 7.02 (1H, d, J=9.0 Hz), 7.29 (2H, d, J=8.0 Hz), 7.52-7.71 (7H, m), 7.76 (1H, d, J=2.5 Hz), 8.20 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 57; Yield: 33% (white solid).
1H-NMR (CDCl3) δ: 2.74 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 5.18 (2H, s), 6.95 (1H, d, J=8.0 Hz), 7.23-7.25 (2H, m), 7.38 (1H, dd, J=8.0, 2.0 Hz), 7.41 (1H, d, J=2.0 Hz), 7.50-7.54 (3H, m), 7.59-7.65 (2H, m), 7.71 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 3,5-dimethylbenzyl bromide; Yield: 51% (white solid).
1H-NMR (CDCl3) δ: 2.35 (6H, s), 5.17 (2H, s), 7.00 (1H, s), 7.06 (2H, s), 7.14 (1H, d, J=9.0 Hz), 7.25-7.29 (2H, m), 7.55-7.60 (2H, m), 7.73 (1H, dd, J=9.0, 2.5 Hz), 8.07 (1H, d, J=2.5 Hz), 10.60 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 59(1) and malonic acid; Yield: 64% (white solid).
1H-NMR (CDCl3) δ: 2.34 (6H, s), 5.16 (2H, s), 6.66 (1H, d, J=16.0 Hz), 6.98 (1H, s), 7.04 (1H, d, J=8.5 Hz), 7.06 (2H, s), 7.26-7.29 (2H, m), 7.51 (1H, dd, J=8.5, 2.5 Hz), 7.53-7.56 (2H, m), 7.73 (1H, d, J=2.5 Hz), 8.19 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 59(2); Yield: 59% (white solid).
1H-NMR (CDCl3) δ: 2.33 (6H, s), 2.74 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 5.06 (2H, s), 6.96 (1H, s), 6.96 (1H, d, J=8.5 Hz), 7.05 (2H, s), 7.22-7.25 (2H, m), 7.36 (1H, dd, J=8.5, 2.5 Hz), 7.39 (1H, d, J=2.5 Hz), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-methoxybenzyl bromide; Yield: 84% (white solid).
1H-NMR (CDCl3) δ: 3.83 (3H, s), 5.17 (2H, s), 6.93-6.96 (2H, m), 7.16 (1H, d, J=8.5 Hz), 7.26-7.29 (2H, m), 7.37-7.40 (2H, m), 7.56-7.60 (2H, m), 7.73 (1H, dd, J=8.5, 2.5 Hz), 8.06 (1H, d, J=2.5 Hz), 10.55 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 60(1) and malonic acid; Yield: 78% (white solid).
1H-NMR (CDCl3) δ: 3.83 (3H, s), 5.15 (2H, s), 6.62 (1H, d, J=16.0 Hz), 6.93-6.96 (2H, m), 7.06 (1H, d, J=9.0 Hz), 7.26-7.29 (2H, m), 7.38 (2H, d, J=8.5 Hz), 7.52 (1H, dd, J=9.0, 2.0 Hz), 7.55 (2H, d, J=8.5 Hz), 7.72 (1H, d, J=2.0 Hz), 8.16 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 60(2); Yield: 62% (white solid).
1H-NMR (CDCl3) δ: 2.72 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.82 (3H, s), 5.06 (2H, s), 6.91-6.95 (2H, m), 6.98 (1H, d, J=8.5 Hz), 7.23-7.26 (2H, m), 7.34-7.38 (4H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-methylbenzyl bromide; Yield: 65% (white solid).
1H-NMR (CDCl3) δ: 2.38 (3H, s), 5.20 (2H, s), 7.14 (1H, d, J=8.5 Hz), 7.23 (2H, d, J=8.0 Hz), 7.27 (2H, d, J=8.5 Hz), 7.35 (2H, d, J=8.0 Hz), 7.55-7.59 (2H, m), 7.73 (1H, dd, J=8.5, 2.5 Hz), 8.06 (1H, d, J=2.5 Hz), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 61(1) and malonic acid; Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 2.37 (3H, s), 5.19 (2H, s), 6.64 (1H, d, J=16.0 Hz), 7.05 (1H, d, J=8.5 Hz), 7.22 (2H, d, J=8.0 Hz), 7.28 (2H, d, J=8.0 Hz), 7.34 (2H, d, J=8.0 Hz), 7.51 (1H, dd, J=8.5, 2.5 Hz), 7.52-7.56 (2H, m), 7.72 (1H, d, J=2.5 Hz), 8.17 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 61(2); Yield: 39% (white solid).
1H-NMR (CDCl3) δ: 2.36 (3H, s), 2.73 (2H, t, J=7.5 Hz), 3.04 (2H, t, J=7.5 Hz), 5.09 (2H, s), 6.97 (1H, d, J=8.0 Hz), 7.19-7.25 (4H, m), 7.33 (2H, d, J=8.5 Hz), 7.36 (1H, dd, J=8.0, 2.5 Hz), 7.39 (1H, d, J=2.5 Hz), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-(trifluoromethoxy)benzyl bromide; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 5.24 (2H, s), 7.13 (1H, d, J=8.5 Hz), 7.28 (4H, d, J=9.0 Hz), 7.47-7.52 (2H, m), 7.57-7.59 (2H, m), 7.75 (1H, dd, J=8.5, 2.5 Hz), 8.08 (1H, d, J=2.5 Hz), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 62(1) and malonic acid; Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 5.22 (2H, s), 6.62 (1H, d, J=16.0 Hz), 7.03 (1H, d, J=8.5 Hz), 7.27-7.30 (4H, m), 7.47-7.58 (5H, m), 7.75 (1H, d, J=2.5 Hz), 8.20 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 62(2); Yield: 36% (white solid).
1H-NMR (CDCl3) δ: 2.73 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 5.13 (2H, s), 6.95 (1H, d, J=8.5 Hz), 7.23-7.26 (4H, m), 7.37 (1H, dd, J=8.5, 2.5 Hz), 7.41 (1H, d, J=2.5 Hz), 7.45-7.48 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 28% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.20 (2H, s), 6.64 (1H, d, J=15.9 Hz), 7.07 (1H, d, J=8.7 Hz), 7.17-7.24 (1H, m), 7.26-7.50 (7H, m), 7.54 (1H, dd, J=2.4, 8.7 Hz), 7.75 (1H, d, J=2.4 Hz), 8.20 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 63; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.75 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 5.12 (2H, s), 6.99 (1H, d, J=8.4 Hz), 7.11-7.16 (1H, m), 7.34-7.48 (9H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 31(1) and 2-(trifluoromethoxy)phenylboronic acid; Yield: 24% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.19 (2H, s), 6.58 (1H, d, J=16.2 Hz), 7.06 (1H, d, J=8.7 Hz), 7.33-7.48 (9H, m), 7.66 (1H, d, J=2.1 Hz), 8.19 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 65; Yield: 71% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.73 (2H, t, J=7.5 Hz), 3.05 (2H, t, J=7.5 Hz), 5.11 (2H, s), 6.98 (1H, d, J=9.3 Hz), 7.27-7.45 (10H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 5-bromosalicylaldehyde and 4-(tert-butyl)phenylboronic acid; Yield: 64% (white solid).
1H-NMR (CDCl3) δ: 1.37 (9H, s), 7.06 (1H, d, J=8.7 Hz), 7.45-7.52 (4H, m), 7.74-7.79 (2H, m), 9.97 (1H, s), 10.98 (1H, s).
The title compound was obtained in the same manner as the Example 31(1) using the following starting materials.
Starting materials: the intermediate 67(1) and triethyl phosphonoacetate; Yield: 70% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 1.36 (3H, t, J=7.2 Hz), 4.30 (2H, q, J=7.2 Hz), 6.26 (1H, s), 6.69 (1H, d, J=16.2 Hz), 6.90 (1H, d, J=8.1 Hz), 7.42-7.50 (5H, m), 7.68 (1H, d, J=2.1 Hz), 8.06 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 67(2); Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.35 (9H, s), 2.75 (2H, t, J=5.7 Hz), 2.95 (2H, t, J=5.7 Hz), 4.15 (2H, q, J=7.2 Hz), 6.94 (1H, d, J=8.4 Hz), 7.29-7.37 (3H, m), 7.40-7.49 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 67(3) and 2-(trifluoromethoxy)benzyl bromide; Yield: 99% (colorless oil).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.2 Hz), 1.36 (9H, s), 2.68 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 4.12 (2H, q, J=7.2 Hz), 5.22 (2H, s), 6.94 (1H, d, J=8.4 Hz), 7.30-7.50 (9H, m), 7.63-7.66 (1H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 67(4); Yield: 99% (white solid).
1H-NMR (DMSO-d6) δ: 1.31 (9H, s), 2.49-2.56 (2H, m), 2.87 (2H, t, J=7.8 Hz), 5.21 (2H, s), 7.13 (1H, d, J=9.0 Hz), 7.42-7.53 (9H, m), 7.66-7.72 (1H, m), 12.06 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 67(3) and 3-(trifluoromethoxy)benzyl bromide; Yield: 99% (colorless oil).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.2 Hz), 1.36 (9H, s), 2.67 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 4.12 (2H, q, J=7.2 Hz), 5.14 (2H, s), 6.92 (1H, d, J=8.7 Hz), 7.15-7.19 (1H, m), 7.33-7.50 (9H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 68(1); Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 1.31 (9H, s), 2.56 (2H, t, J=7.8 Hz), 2.92 (2H, t, J=7.8 Hz), 5.25 (2H, s), 7.09 (1H, d, J=8.7 Hz), 7.32-7.35 (1H, m), 7.42-7.58 (9H, m), 12.09 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 67(3) and 4-chlorobenzyl bromide; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.2 Hz), 1.35 (9H, s), 2.66 (2H, t, J=7.5 Hz), 3.05 (2H, t, J=7.5 Hz), 4.12 (2H, q, J=7.2 Hz), 5.09 (2H, s), 6.91 (1H, d, J=8.1 Hz), 7.32-7.49 (10H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 69(1); Yield: 66% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 2.56 (2H, t, J=7.8 Hz), 2.89 (2H, t, J=7.8 Hz), 5.18 (2H, s), 7.03-7.09 (1H, m), 7.40-7.53 (10H, m), 12.09 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 67(3) and 4-(trifluoromethyl)benzyl bromide; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.2 Hz), 1.35 (9H, s), 2.68 (2H, t, J=7.5 Hz), 3.08 (2H, t, J=7.5 Hz), 4.12 (2H, q, J=7.2 Hz), 5.18 (2H, s), 6.91 (1H, d, J=8.1 Hz), 7.38-7.49 (6H, m), 7.56-7.58 (2H, m), 7.65-7.67 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 70(1); Yield: 78% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 2.58 (2H, t, J=7.8 Hz), 2.93 (2H, t, J=7.8 Hz), 5.30 (2H, s), 7.08 (1H, d, J=8.4 Hz), 7.41-7.47 (4H, m), 7.51-7.53 (2H, m), 7.69-7.72 (2H, m), 7.77-7.79 (2H, m), 12.10 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 67(3) and 4-butylbenzyl chloride; Yield: 99% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.22 (3H, t, J=7.2 Hz), 1.32-1.39 (11H, m), 1.54-1.66 (2H, m), 2.59-2.70 (4H, m), 3.02-3.10 (2H, m), 4.10-4.17 (2H, m), 5.09 (2H, s), 6.96 (1H, d, J=8.1 Hz), 7.19-7.22 (2H, m), 7.34-7.49 (8H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 71(1); Yield: 92% (white solid).
1H-NMR (DMSO-d6) δ: 0.90 (3H, t, J=7.2 Hz), 1.25-1.37 (11H, m), 1.51-1.61 (2H, m), 2.50-2.61 (4H, m), 2.89 (2H, t, J=7.8 Hz), 5.13 (2H, s), 7.09 (1H, d, J=9.0 Hz), 7.21-7.23 (2H, m), 7.36-7.45 (6H, m), 7.50-7.52 (2H, m), 12.09 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 2,4-difluorobenzaldehyde and 4-isopropylphenol; Yield: 97.6% (brown oil).
1H-NMR (CDCl3) δ: 1.24 (6H, d, J=6.9 Hz), 1.25 (6H, d, J=6.9 Hz), 2.85-2.96 (2H, m), 6.44 (1H, d, J=2.4 Hz), 6.11 (1H, dd, J=2.4, 9.0 Hz), 6.92-6.96 (2H, m), 6.98-7.02 (2H, m), 7.19-7.26 (4H, m), 7.86 (1H, d, J=9.0 Hz), 10.40 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 72(1) and malonic acid; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.22 (6H, d, J=2.7 Hz), 1.25 (6H, d, J=2.4 Hz), 2.84-2.94 (2H, m), 6.47 (1H, d, J=2.1 Hz), 6.50 (1H, d, J=16.2 Hz), 6.60 (1H, dd, J=2.1, 8.7 Hz), 6.89-6.98 (4H, m), 7.15-7.22 (4H, m), 7.53 (1H, d, J=8.7 Hz), 8.07 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 72; Yield: 74.0% (white solid).
1H-NMR (CDCl3) δ: 1.21 (6H, d, J=2.4 Hz), 1.24 (6H, d, J=2.4 Hz), 2.70 (2H, t, J=7.5 Hz), 2.82-2.94 (2H, m), 2.96 (2H, t, J=7.5 Hz), 6.53 (1H, d, J=2.1 Hz), 6.61 (1H, dd, J=2.1, 8.4 Hz), 6.86-6.92 (4H, m), 7.12-7.18 (5H, m).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 72(1) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate; Yield: 95.4% (yellow oil).
1H-NMR (CDCl3) δ: 1.22 (6H, s), 1.24 (6H, s), 2.81-2.96 (2H, m), 3.70 (3H, s), 5.91 (1H, d, J=12.6 Hz), 6.50 (1H, d, J=2.4 Hz), 6.63 (1H, dd, J=2.4, 8.4 Hz), 6.89-6.95 (4H, m), 7.14-7.18 (5H, m), 7.77 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 74(1); Yield: 74.3% (white solid).
1H-NMR (CDCl3) δ: 1.22 (6H, s), 1.24 (6H, s), 2.83-2.93 (2H, m), 5.92 (1H, d, J=12.6 Hz), 6.48 (1H, d, J=2.4 Hz), 6.60 (1H, dd, J=2.4, 8.7 Hz), 6.90-6.95 (4H, m), 7.15-7.19 (4H, m), 7.26 (1H, d, J=12.6 Hz), 7.77 (1H, d, J=8.7 Hz).
A mixture of 4-bromo-2-fluorobenzaldehyde (2.00 g, 9.85 mmol), 4-(tert-butyl)benzyl alcohol (1.78 g, 10.84 mmol), potassium carbonate (2.04 g, 14.78 mmol) and dimethylformamide (4 ml) was stirred at 120° C. for 8 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=20:1) to give the title compound (893 mg, 17.4%) as a yellow oil.
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.14 (2H, s), 7.18-7.22 (1H, m), 7.26-7.34 (1H, m), 7.37 (2H, d, J=8.4 Hz), 7.45 (2H, d, J=8.4 Hz), 7.72 (1H, d, J=8.1 Hz), 10.46 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 75(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 61.5% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 5.23 (2H, s), 7.22 (1H, s), 7.24-7.26 (1H, m), 7.31-7.34 (1H, m), 7.39-7.48 (4H, m), 7.59-7.62 (2H, m), 7.92-7.95 (2H, m), 10.57 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 75(2) and malonic acid; Yield: 93.6% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 5.23 (2H, s), 6.60 (1H, d, J=16.2 Hz), 7.15-7.20 (2H, m), 7.29 (2H, d, J=8.1 Hz), 7.39-7.47 (4H, m), 7.55-7.58 (2H, m), 7.64 (1H, d, J=8.1 Hz), 8.18 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 75; Yield: 78.3% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.74 (2H, t, J=7.2 Hz), 3.05 (2H, t, J=7.2 Hz), 5.13 (2H, s), 7.06-7.09 (2H, m), 7.25-7.28 (3H, m), 7.37-7.45 (4H, m), 7.52-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 15(1) using the following starting materials.
Starting materials: the intermediate 75(1) and 4-(trifluoromethoxy)phenol; Yield: 21.7% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.09 (2H, s), 6.56 (1H, dd, J=2.1, 8.4 Hz), 6.62 (1H, d, J=2.1 Hz), 7.04-7.08 (1H, m), 7.25 (2H, d, J=8.4 Hz), 7.31 (2H, d, J=8.4 Hz), 7.42 (2H, d, J=8.4 Hz), 7.84 (2H, d, J=8.4 Hz), 10.43 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 77(1) and malonic acid; Yield: 92.6% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.09 (2H, s), 6.49 (1H, d, J=16.2 Hz), 6.55 (1H, dd, J=2.1, 8.4 Hz), 6.61 (1H, d, J=2.1 Hz), 6.99-7.03 (2H, m), 7.20 (2H, d, J=8.7 Hz), 7.26-7.31 (2H, m), 7.39-7.42 (2H, m), 7.51 (1H, d, J=8.4 Hz), 8.09 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 77; Yield: 80.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.69 (2H, t, J=7.8 Hz), 2.97 (2H, t, J=7.8 Hz), 5.00 (2H, s), 6.50 (1H, dd, J=2.4, 8.1 Hz), 6.62 (1H, d, J=2.4 Hz), 6.94-6.97 (2H, m), 7.11-7.16 (3H, m), 7.30 (2H, d, J=8.1 Hz), 7.38-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-(tert-butyl)phenol; Yield: 75.9% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 6.99-7.05 (3H, m), 7.27-7.31 (1H, m), 7.41-7.47 (2H, m), 7.78 (1H, d, J=8.1 Hz), 10.49 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 79(1) and malonic acid; Yield: 65% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 6.64 (1H, d, J=16.0 Hz), 6.96-7.01 (3H, m), 7.39 (1H, dd, J=2.0, 8.5 Hz), 7.43-7.46 (2H, m), 7.74 (1H, d, J=16.0 Hz), 7.85 (1H, d, J=8.5 Hz), 12.51 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 96% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 6.65 (1H, d, J=16.0 Hz), 6.91-6.96 (2H, m), 7.25 (1H, d, J=2.0 Hz), 7.37-7.43 (4H, m), 7.55 (1H, dd, J=2.0, 8.5 Hz), 7.74-7.77 (2H, m), 7.77 (1H, d, J=16.0 Hz), 8.01 (1H, d, J=8.0 Hz), 12.48 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 79; Yield: 93% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.55 (2H, t, J=7.5 Hz), 2.84 (2H, t, J=7.5 Hz), 6.87-6.92 (2H, m), 7.15 (1H, s), 7.34-7.47 (6H, m), 7.68-7.72 (2H, m), 12.18 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 5-bromo-2-hydroxy-3-methoxybenzaldehyde and 4-(tert-butyl)benzyl bromide; Yield: 96% (colorless oil).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 3.95 (3H, s), 5.11 (2H, s), 7.30 (1H, d, J=2.5 Hz), 7.32 (2H, d, J=8.0 Hz), 7.39 (2H, d, J=8.0 Hz), 7.58 (1H, d, J=2.5 Hz), 9.98 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 81(1) and malonic acid; Yield: 76% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 3.88 (3H, s), 4.92 (2H, s), 6.48 (1H, d, J=16.0 Hz), 7.29-7.31 (2H, m), 7.30 (1H, d, J=2.0 Hz), 7.36-7.39 (2H, m), 7.51 (1H, d, J=2.0 Hz), 7.64 (1H, d, J=16.0 Hz), 12.38 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 81(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 31% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 3.97 (3H, s), 4.97 (2H, s), 6.64 (1H, d, J=16.0 Hz), 7.34-7.46 (7H, m), 7.62 (1H, d, J=2.0 Hz), 7.81 (1H, d, J=16.0 Hz), 7.91 (2H, d, J=8.5 Hz), 12.34 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 81; Yield: 63% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.44 (2H, t, J=7.5 Hz), 2.83 (2H, t, J=7.5 Hz), 3.93 (3H, s), 4.95 (2H, s), 7.11 (1H, d, J=2.0 Hz), 7.21 (1H, d, J=2.0 Hz), 7.36-7.45 (6H, m), 7.77-7.80 (2H, m), 12.09 (1H, s).
Boron tribromide (2.0 ml, 21.116 mmol) was added dropwise to a solution of 5-bromo-2-methoxytoluene (2.108 g, 10.486 mmol) in dichloromethane (20 ml) at −78° C., and the mixture was stirred at 0° C. for 6 hours. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15:1) to give the title compound (1.942 g, 99%) as a white solid.
1H-NMR (CDCl3) δ: 2.22 (3H, s), 4.83 (1H, s), 6.65 (1H, d, J=8.4 Hz), 7.16 (1H, dd, J=2.4, 8.4 Hz), 7.23 (1H, d, J=2.4 Hz).
Triethylamine (2.5 ml, 17.94 mmol) was added to a mixture of paraformaldehyde (811 mg, 27.00 mmol), magnesium chloride (1.714 g, 18.00 mmol) and tetrahydrofuran (45 ml), and the mixture was stirred at room temperature for 20 minutes. The intermediate 83(1) (1.683 g, 9.00 mmol) was added to the reaction mixture, and the mixture was refluxed for 8 hours. The reaction mixture was cooled to room temperature, and diluted with ethyl acetate. The organic layer was washed with 1 N hydrochloric acid, water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (714 mg, 36.9%) as a yellowish-orange solid.
1H-NMR (CDCl3) δ: 2.26 (3H, s), 7.49-7.52 (2H, m), 9.82 (1H, s), 11.19 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 83(2) and 4-(tert-butyl)benzyl bromide; Yield: 53% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.34 (3H, s), 4.92 (2H, s), 7.30-7.33 (2H, m), 7.41-7.44 (2H, m), 7.58-7.59 (1H, m), 7.78-7.89 (1H, m), 10.13 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 83(3) and malonic acid; Yield: 76% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.30 (3H, s), 4.77 (2H, s), 6.38 (1H, d, J=16.1 Hz), 7.34-7.44 (5H, m), 7.54-7.55 (1H, m), 7.97 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 83(4) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 41% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.40 (3H, s), 4.84 (2H, s), 6.51 (1H, d, J=16.1 Hz), 7.26-7.31 (2H, m), 7.40-7.46 (5H, m), 7.57-7.60 (3H, m), 8.14 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 83; Yield: 91% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.40 (3H, s), 2.71 (2H, t, J=7.8 Hz), 3.04 (2H, t, J=7.8 Hz), 4.84 (2H, s), 7.24-7.27 (4H, m), 7.44 (4H, s), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 83(1) using the following starting material.
Starting material: 2-fluoro-6-methoxybenzaldehyde; Yield: 82% (reddish purple solid).
1H-NMR (CDCl3) δ: 6.60-6.67 (1H, m), 6.75-6.78 (1H, m), 7.43-7.51 (1H, m), 10.27 (1H, s), 11.43 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 85(1) and 4-(tert-butyl)benzyl bromide; Yield: 91% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.16 (2H, s), 6.71-6.77 (1H, m), 6.85 (1H, d, J=8.4 Hz), 7.35-7.50 (5H, m), 10.50 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 85(2) and 4-(trifluoromethoxy)phenol; Yield: 85% (brown solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.18 (2H, s), 6.49 (1H, d, J=8.4 Hz), 6.83 (1H, d, J=8.6 Hz), 7.01-7.04 (2H, m), 7.18-7.21 (2H, m), 7.38-7.45 (5H, m), 10.57 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 85(3) and malonic acid; Yield: 82% (flesh-colored solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.19 (2H, s), 6.46 (1H, d, J=8.4 Hz), 6.77 (1H, d, J=8.4 Hz), 6.94 (1H, d, J=16.3 Hz), 6.99-7.03 (2H, m), 7.18-7.27 (3H, m), 7.36-7.44 (4H, m), 8.20 (1H, d, J=16.3 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 85; Yield: 96% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.59 (2H, t, J=7.9 Hz), 3.05 (2H, t, J=7.9 Hz), 5.09 (2H, s), 6.50 (1H, d, J=8.2 Hz), 6.75 (1H, d, J=8.2 Hz), 6.92-6.95 (2H, m), 7.10-7.16 (3H, m), 7.34-7.43 (4H, m).
The title compound was obtained in the same manner as the Example 83(2) using the following starting materials.
Starting materials: 2-bromophenol and paraformaldehyde; Yield: 33% (yellow solid).
1H-NMR (CDCl3) δ: 6.93-6.98 (1H, m), 7.54-7.57 (1H, m), 7.78-7.81 (1H, m), 9.87 (1H, s), 11.62 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 87(1) and 4-(tert-butyl)benzyl bromide; Yield: 97% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.09 (2H, s), 7.15 (1H, t, J=7.7 Hz), 7.37-7.45 (4H, m), 7.78 (1H, dd, J=1.6, 7.7 Hz), 7.85 (1H, dd, J=1.6, 7.7 Hz), 10.14 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 87(2) and malonic acid; Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.94 (2H, s), 6.40 (1H, d, J=16.1 Hz), 7.04-7.09 (1H, m), 7.42-7.47 (4H, m), 7.51-7.54 (1H, m), 7.64-7.67 (1H, m), 8.00 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 87(3) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 43% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 4.23 (2H, s), 6.51 (1H, d, J=16.1 Hz), 6.93-6.96 (2H, m), 7.23-7.29 (5H, m), 7.39-7.42 (1H, m), 7.56-7.64 (3H, m), 8.18 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 87; Yield: 85% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.73 (2H, t, J=7.8 Hz), 3.06 (2H, t, J=7.8 Hz), 4.37 (2H, s), 2.97-7.00 (2H, m), 7.12-7.31 (7H, m), 7.59-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 83(1) using the following starting material.
Starting material: 2-fluoro-4-methoxybenzaldehyde; Yield: 68% (white solid).
1H-NMR (DMSO-d6) δ: 6.68 (1H, dd, J=2.0, 13.0 Hz), 6.76 (1H, dd, J=2.0, 8.5 Hz), 7.07 (1H, t, J=8.5 Hz), 10.01 (1H, s), 11.13 (1H, s).
A mixture of the intermediate 89(1) (500 mg, 3.563 mmol), 4-(trifluoromethoxy)phenylboronic acid (1.46 g, 7.136 mmol), copper(II) acetate (648 mg, 3.568 mmol), triethylamine (2.5 ml, 17.84 mmol), molecular sieves 4A and dichloromethane (35 ml) was stirred at room temperature for 2 hours. The reaction mixture was filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was diluted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (132 mg, 12%) as a yellow oil.
1H-NMR (CDCl3) δ: 6.69 (1H, dd, J=2.5, 11.5 Hz), 6.82-6.86 (1H, m), 7.11-7.15 (2H, m), 7.30 (2H, d, J=9.0 Hz), 7.86 (1H, t, J=8.5 Hz), 10.25 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 89(2) and 4-(tert-butyl)phenol; Yield: 54% (yellow oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 6.45 (1H, d, J=2.0 Hz), 6.63 (1H, dd, J=2.0, 8.5 Hz), 6.99-7.04 (4H, m), 7.19-7.22 (2H, m), 7.38-7.41 (2H, m), 7.90 (1H, d, J=8.5 Hz), 10.42 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 89(3) and malonic acid; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 6.49 (1H, d, J=2.5 Hz), 6.52 (1H, d, J=16.0 Hz), 6.54 (1H, dd, J=2.5, 8.5 Hz), 6.94-7.01 (4H, m), 7.16-7.19 (2H, m), 7.35-7.38 (2H, m), 7.58 (1H, d, J=8.5 Hz), 8.08 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 89; Yield: 87% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.72 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5 Hz), 6.53 (1H, d, J=2.5 Hz), 6.63 (1H, dd, J=2.5, 8.5 Hz), 6.88-6.96 (4H, m), 7.12-7.15 (2H, m), 7.22 (1H, d, J=8.5 Hz), 7.31-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 83(2) using the following starting materials.
Starting materials: 4-bromo-2-chlorophenol and paraformaldehyde; Yield: 13% (yellow solid).
1H-NMR (CDCl3) δ: 7.63 (1H, d, J=2.5 Hz), 7.75 (1H, d, J=2.5 Hz), 9.85 (1H, s), 11.39 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 91(1) and 4-(tert-butyl)benzyl bromide; Yield: 94% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.10 (2H, s), 7.29-7.32 (2H, m), 7.39-7.42 (2H, m), 7.80-7.81 (2H, m), 9.97 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 91(2) and malonic acid; Yield: 30% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.95 (2H, s), 6.34 (1H, d, J=16.0 Hz), 7.37 (2H, dd, J=2.5, 8.5 Hz), 7.42 (2H, dd, J=2.5, 8.5 Hz), 7.58 (1H, d, J=2.5 Hz), 7.62 (1H, d, J=2.5 Hz), 7.84 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 91(3) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 39% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.00 (2H, s), 6.46 (1H, d, J=16.0 Hz), 7.32 (2H, d, J=8.5 Hz), 7.43 (4H, s), 7.56-7.59 (2H, m), 7.62 (1H, d, J=2.0 Hz), 7.67 (1H, d, J=2.0 Hz), 7.99 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 91; Yield: 73% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 2.56 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 4.95 (2H, s), 7.44-7.46 (6H, m), 7.58 (1H, d, J=2.0 Hz), 7.70 (1H, d, J=2.0 Hz), 7.81 (2H, d, J=8.5 Hz), 12.17 (1H, s).
Trifluoromethanesulfonic anhydride (672 mg, 2.381 mmol), 4-dimethylaminopyridine (23 mg, 0.189 mmol) and triethylamine (0.32 ml, 2.296 mmol) were added to a solution of the intermediate 85(1) (266 mg, 1.899 mmol) in dichloromethane (4 ml) at 0° C. under argon atmosphere, and the mixture was stirred at room temperature for 20 hours. A saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (384 mg, 74.2%) as a white solid.
1H-NMR (CDCl3) δ: 7.18-7.33 (2H, m), 7.65-7.73 (1H, m), 10.38 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 93(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 78% (colorless oil).
1H-NMR (CDCl3) δ: 7.17-7.38 (6H, m), 7.56-7.63 (1H, m), 10.04 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 93(2) and 4-(tert-butyl)phenol; Yield: 43% (yellow solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 6.92-6.95 (1H, m), 6.98-7.04 (3H, m), 7.26-7.28 (2H, m), 7.34-7.49 (5H, m), 10.33 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 93(3) and malonic acid; Yield: 68% (flesh-colored solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.64 (1H, d, J=16.3 Hz), 6.87-7.04 (4H, m), 7.26-7.40 (7H, m), 7.65 (1H, d, J=16.3 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 93; Yield: 47% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.53-2.59 (2H, m), 2.90-2.96 (2H, m), 6.83-6.95 (4H, m), 7.14-7.20 (1H, m), 7.24-7.26 (2H, m), 7.31-7.37 (4H, m).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: 4-(trifluoromethoxy)phenylboronic acid and 4-hydroxybenzaldehyde; Yield: 49% (yellow solid).
1H-NMR (CDCl3) δ: 7.07-7.12 (4H, m), 7.25-7.28 (2H, m), 7.85-7.90 (2H, m), 9.95 (1H, s).
m-Chloroperbenzoic acid (690 mg, 3.079 mmol) was added to a solution of the intermediate 95(1) (695 mg, 2.463 mmol) in chloroform (6.8 ml), and the mixture was stirred at room temperature for 2 hours. A saturated aqueous solution of sodium hydrogen sulfite was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. Methanol (20 ml) and catalytic amount of concentrated hydrochloric acid were added to the residue obtained by evaporation of the solvent under reduced pressure, and the mixture was stirred at room temperature for 30 minutes. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (561 mg, 84.3%) as a colorless oil.
1H-NMR (CDCl3) δ: 4.64 (1H, s), 6.81-6.86 (2H, m), 6.90-6.96 (4H, m), 7.12-7.16 (2H, m).
The title compound was obtained in the same manner as the Example 83(2) using the following starting materials.
Starting materials: the intermediate 95(2) and paraformaldehyde; Yield: 39% (colorless oil).
1H-NMR (CDCl3) δ: 6.93-7.04 (3H, m), 7.17-7.29 (4H, m), 9.84 (1H, s), 10.85 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 95(3) and 4-(tert-butyl)benzyl bromide; Yield: 94% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.16 (2H, s), 6.93-6.97 (2H, m), 7.07-7.24 (4H, m), 7.36-7.50 (5H, m), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 95(4) and malonic acid; Yield: 68% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.13 (2H, s), 6.47 (1H, d, J=16.1 Hz), 6.92-7.05 (4H, m), 7.15-7.26 (3H, m), 7.35-7.45 (4H, m), 8.11 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 95; Yield: 94% (white oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.69 (2H, t, J=7.5 Hz), 2.97 (2H, t, J=7.5 Hz), 5.05 (2H, s), 6.83-6.94 (5H, m), 7.11-7.14 (2H, m), 7.34-7.43 (4H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 2,6-difluorobenzaldehyde and 4-(trifluoromethoxy)phenol; Yield: 11% (white solid).
1H-NMR (CDCl3) δ: 6.64 (2H, d, J=8.5 Hz), 7.07-7.10 (4H, m), 7.23-7.26 (4H, m), 7.40 (1H, t, J=8.5 Hz), 10.55 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 97(1) and malonic acid; Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 6.60 (2H, d, J=8.5 Hz), 6.92 (1H, d, J=16.5 Hz), 7.04-7.09 (4H, m), 7.21 (1H, t, J=8.5 Hz), 7.22-7.26 (4H, m), 8.13 (1H, d, J=16.5 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 97; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 2.60-2.65 (2H, m), 3.02-3.07 (2H, m), 6.64 (2H, d, J=8.0 Hz), 6.98-7.02 (4H, m), 7.13 (1H, t, J=8.0 Hz), 7.18-7.21 (4H, m).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: the intermediate 95(3) and 4-(tert-butyl)phenylboronic acid; Yield: 94% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.93-6.97 (2H, m), 7.07-7.24 (4H, m), 7.36-7.50 (5H, m), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 99(1) and malonic acid; Yield: 98% (ocherous solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 6.49 (1H, d=16.1 Hz), 6.88-7.02 (6H, m), 7.18-7.21 (2H, m), 7.28-7.29 (1H, m), 7.35-7.38 (2H, m), 8.04 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 99; Yield: 92% (yellow oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.69 (2H, t, J=7.6 Hz), 2.94 (2H, t, J=7.6 Hz), 6.80-6.90 (4H, m), 6.95-6.99 (3H, m), 7.15-7.18 (2H, m), 7.31-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 3-phenylpropyl bromide; Yield: 74.3% (yellow solid).
1H-NMR (CDCl3) δ: 2.18-2.27 (2H, m), 2.87 (2H, t, J=7.5 Hz), 4.14 (2H, t, J=6.3 Hz), 7.02 (1H, d, J=8.4 Hz), 7.20-7.34 (7H, m), 7.56-7.59 (2H, m), 7.72 (1H, dd, J=2.4, 8.4 Hz), 8.05 (1H, d, J=2.4 Hz), 10.53 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 101(1) and malonic acid; Yield: 62.8% (white solid).
1H-NMR (CDCl3) δ: 2.18-2.27 (2H, m), 2.88 (2H, t, J=7.5 Hz), 4.10 (2H, t, J=6.3 Hz), 6.68 (1H, d, J=16.2 Hz), 6.96 (1H, d, J=8.4 Hz), 7.19-7.33 (7H, m), 7.51-7.58 (3H, m), 7.72 (1H, d, J=2.1 Hz), 8.16 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 101(2); Yield: 79.7% (white solid).
1H-NMR (DMSO-d6) δ: 2.03-2.09 (2H, m), 2.57 (2H, t, J=7.8 Hz), 2.79 (2H, t, J=7.8 Hz), 2.89 (2H, t, J=7.8 Hz), 4.02 (2H, t, J=6.0 Hz), 7.01 (1H, d, J=9.3 Hz), 7.16-7.32 (5H, m), 7.39-7.42 (2H, m), 7.46-7.49 (2H, m), 7.70-7.73 (2H, m), 12.13 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-phenylbutyl bromide; Yield: 74.3% (yellow solid).
1H-NMR (CDCl3) δ: 1.82-1.94 (4H, m), 2.71-2.76 (2H, m), 4.12-4.18 (2H, m), 7.04 (1H, d, J=8.7 Hz), 7.19-7.30 (7H, m), 7.56-7.59 (2H, m), 7.73 (1H, dd, J=2.4, 8.7 Hz), 8.04 (1H, d, J=2.4 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 102(1) and malonic acid; Yield: 82.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.85-1.91 (4H, m), 2.73 (2H, t, J=7.2 Hz), 4.11 (2H, t, J=6.0 Hz), 6.64 (1H, d, J=16.2 Hz), 6.98 (1H, d, J=8.4 Hz), 7.19-7.33 (7H, m), 7.52-7.57 (3H, m), 7.71 (1H, d, J=2.1 Hz), 8.14 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 102(2); Yield: 57.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.76-1.80 (4H, m), 2.53 (2H, t, J=7.8 Hz), 2.64-2.68 (2H, m), 2.85 (2H, t, J=7.8 Hz), 4.03-4.08 (2H, m), 7.03 (1H, d, J=9.0 Hz), 7.14-7.31 (5H, m), 7.38-7.42 (2H, m), 7.46-7.50 (2H, m), 7.68-7.73 (2H, m), 12.10 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 54(2) and 3-phenoxypropyl bromide; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.21 (3H, t, J=7.2 Hz), 2.27-2.36 (2H, m), 2.62 (2H, t, J=7.8 Hz), 3.00 (2H, t, J=7.5 Hz), 4.07-4.25 (6H, m), 6.88-6.98 (4H, m), 7.22-7.32 (4H, m), 7.34-7.39 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 103(1); Yield: 58.5% (white solid).
1H-NMR (CDCl3) δ: 2.31 (2H, quintet, J=7.5 Hz), 2.69 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 4.19 (2H, t, J=6.0 Hz), 4.23 (2H, t, J=6.0 Hz), 6.90-6.97 (4H, m), 7.22-7.31 (4H, m), 7.36-7.40 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 5-phenylpentyl chloride; Yield: 100% (brown oil).
1H-NMR (CDCl3) δ: 1.52-1.58 (2H, m), 1.68-1.74 (2H, m), 1.88-1.94 (2H, m), 2.64-2.69 (2H, m), 4.10-4.14 (2H, m), 7.05 (1H, d, J=8.7 Hz), 7.16-7.21 (3H, m), 7.26-7.31 (4H, m), 7.56-7.59 (2H, m), 7.73 (1H, dd, J=2.7, 8.7 Hz), 8.04 (1H, d, J=2.7 Hz), 10.53 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 104(1) and malonic acid; Yield: 97.3% (white solid).
1H-NMR (CDCl3) δ: 1.51-1.61 (2H, m), 1.68-1.79 (2H, m), 1.88-1.97 (2H, m), 2.65-2.70 (2H, m), 4.07-4.11 (2H, m), 6.64 (1H, d, J=16.2 Hz), 6.98 (1H, d, J=8.7 Hz), 7.18-7.21 (2H, m), 7.25-7.31 (5H, m), 7.51-7.57 (3H, m), 7.71 (1H, d, J=2.4 Hz), 8.12 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 104(2); Yield: 40.2% (white solid).
1H-NMR (DMSO-d6) δ: 1.44-1.53 (2H, m), 1.60-1.70 (2H, m), 1.74-1.83 (2H, m), 2.49-2.51 (2H, m), 2.58-2.63 (2H, m), 2.81-2.86 (2H, m), 4.00-4.04 (2H, m), 7.01-7.04 (1H, m), 7.15-7.29 (5H, m), 7.39-7.41 (2H, m), 7.46-7.50 (2H, m), 7.69-7.72 (2H, m), 12.09 (1H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 4(2); Yield: 95.0% (milky white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 5.12 (2H, s), 5.72 (1H, s), 6.99-7.04 (2H, m), 7.16-7.17 (1H, m), 7.23-7.26 (2H, m), 7.36-7.46 (4H, m), 7.52-7.56 (2H, m).
A mixture of the intermediate 105(1) (158 mg, 0.379 mmol), ethyl bromoacetate (75 mg, 0.451 mmol), potassium carbonate (210 mg, 1.517 mmol) and dimethylformamide (0.75 ml) was stirred at 50° C. for 2 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (185 mg, 97.2%) as a white solid.
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 1.33 (9H, s), 4.24 (2H, q, J=7.1 Hz), 4.75 (2H, s), 5.16 (2H, s), 7.00-7.03 (1H, m), 7.13-7.16 (2H, m), 7.23-7.26 (2H, m), 7.41 (4H, s), 7.49-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 105(2); Yield: 94.0% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, m), 4.73 (2H, s), 5.16 (2H, s), 7.07-7.10 (1H, m), 7.19-7.28 (4H, m), 7.36-7.45 (4H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 105(1) and ethyl 2-bromoisobutyrate; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.1 Hz), 1.33 (9H, s), 1.59 (6H, s), 4.16 (2H, q, J=7.1 Hz), 5.09 (2H, s), 6.98-7.01 (1H, m), 7.15-7.22 (4H, m), 7.37-7.43 (4H, m), 7.48-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 106(1); Yield: 99.0% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.57 (6H, s), 5.17 (2H, s), 7.08-7.11 (1H, m), 7.22-7.37 (6H, m), 7.41-7.44 (2H, m), 7.50-7.53 (2H, m).
Sodium borohydride (35 mg, 0.934 mmol) was added to a solution of the intermediate 4(2) (400 mg, 0.934 mmol) in methanol (10 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was neutralized by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue was evaporated under reduced pressure to give the title compound (394 mg, 98%) as a white solid.
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.35 (1H, brs), 4.79 (2H, s), 5.14 (2H, s), 7.05 (1H, d, J=8.4 Hz), 7.23-7.29 (2H, m), 7.35-7.49 (5H, m), 7.51-7.59 (3H, m).
A solution of intermediate 107(2) (129 mg, 0.30 mmol) in tetrahydrofuran (1 ml) was added dropwise to a mixture of sodium hydride (26 mg, 0.60 mmol) and tetrahydrofuran (2 ml) at 0° C. under argon atmosphere, and the mixture was stirred at room temperature for 30 minutes. Methyl bromoacetate (46 mg, 0.30 mmol) was added to the mixture, and the mixture was stirred at 80° C. for 6 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (42 mg, 28.0%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.73 (3H, s), 4.19 (2H, s), 4.78 (2H, s), 5.10 (2H, s), 7.00-7.03 (1H, m), 7.24-7.27 (2H, m), 7.35-7.47 (5H, m), 7.55-7.58 (2H, m), 7.65-7.67 (1H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 107(2); Yield: 58.9% (whitish-brown solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 4.14 (2H, s), 4.66 (2H, s), 5.16 (2H, s), 7.18 (1H, d, J=8.7 Hz), 7.38-7.43 (6H, m), 7.58 (1H, dd, J=2.1, 8.7 Hz), 7.67 (1H, d, J=2.1 Hz), 7.70-7.74 (2H, m), 12.67 (1H, brs).
Methylmagnesium bromide (0.96 M solution in tetrahydrofuran; 1.46 ml, 1.401 mmol) was added to a solution of the intermediate 4(2) (400 mg, 0.934 mmol) in tetrahydrofuran (10 ml) at 0° C. under argon atmosphere, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (411 mg, 99%) as a white solid.
1H-NMR (CDCl3) δ: 1.34 (9H, s), 1.57 (3H, d, J=6.6 Hz), 2.59 (1H, brs), 5.13 (2H, s), 5.21 (1H, q, J=6.6 Hz), 7.04 (1H, d, J=8.4 Hz), 7.23-7.29 (2H, m), 7.34-7.47 (5H, m), 7.54-7.61 (3H, m).
The title compound was obtained in the same manner as the Example 107(2) using the following starting materials.
Starting materials: the intermediate 108(1) and methyl bromoacetate; Yield: 14.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 1.52-1.62 (3H, m), 3.70 (3H, s), 3.99-4.10 (2H, m), 5.09-5.13 (3H, m), 7.00-7.03 (1H, m), 7.24-7.29 (2H, m), 7.33-7.45 (5H, m), 7.52-7.60 (3H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 108(2); Yield: 50.0% (whitish-brown solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 1.39 (3H, d, J=6.6 Hz), 3.83 (1H, d, J=16.5 Hz), 3.98 (1H, d, J=16.5 Hz), 5.00 (1H, q, J=6.6 Hz), 5.16 (2H, s), 7.19 (1H, d, J=8.4 Hz), 7.36-7.44 (6H, m), 7.56 (1H, dd, J=2.7, 8.4 Hz), 7.63 (1H, d, J=2.7 Hz), 7.71-7.75 (2H, m), 12.60 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 105(1) and ethyl 4-bromobutyrate; Yield: 49% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.1 Hz), 1.33 (9H, s), 2.13-2.22 (2H, m), 2.54-2.59 (2H, m), 4.10-4.17 (4H, m), 5.13 (2H, s), 6.98-7.11 (3H, m), 7.23-7.26 (2H, m), 7.40 (4H, s), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 109(1); Yield: 88% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.15-2.21 (2H, m), 2.60-2.65 (2H, m), 4.13-4.17 (2H, m), 5.13 (2H, s), 6.98-7.11 (3H, m), 7.20-7.26 (2H, m), 7.34-7.40 (4H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.01-7.07 (2H, m), 7.08-7.10 (1H, m), 7.25-7.29 (2H, m), 7.34-7.39 (1H, m), 7.39-7.45 (2H, m), 7.50-7.55 (2H, m), 8.01 (1H, d, J=8.1 Hz), 10.53-10.54 (1H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 110(1); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.61 (1H, s), 6.96-7.02 (2H, m), 7.08-7.13 (2H, m), 7.18-7.26 (3H, m), 7.34-7.39 (2H, m), 7.43-7.49 (2H, m).
Sodium hydroxide (239 mg, 5.968 mmol) was added to a mixture of the intermediate 110(2) (300 mg, 0.746 mmol), 1,1,1-trichloro-2-methyl-2-propanol (chloretone, 256 mg, 1.491 mmol) and acetone (3 ml) at 0° C., and the mixture was refluxed for 4 hours. The reaction mixture was cooled to 0° C., diluted with water, acidified by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (139 mg, 38.1%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.61 (6H, s), 6.92-6.98 (2H, m), 7.15-7.20 (2H, m), 7.22-7.28 (3H, m), 7.33-7.39 (2H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 107(1) using the following starting material.
Starting material: the intermediate 110(1); Yield: 92.5% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.11 (1H, brs), 4.79 (2H, s), 6.93-6.98 (2H, m), 7.06-7.08 (1H, m), 7.22-7.26 (2H, m), 7.31 (1H, dd, J=1.8, 7.8 Hz), 7.33-7.38 (2H, m), 7.47-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 110(3) using the following starting materials.
Starting materials: the intermediate 111(1) and 1,1,1-trichloro-2-methyl-2-propanol (chloretone); Yield: 9.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.55 (6H, s), 4.63 (2H, s), 6.94-6.98 (2H, m), 7.08 (1H, d, J=2.1 Hz), 7.22-7.27 (2H, m), 7.31 (1H, dd, J=2.1, 8.1 Hz), 7.33-7.38 (2H, m), 7.47-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 110(2) and ethyl bromoacetate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.22-1.37 (12H, m), 4.23 (2H, q, J=7.2 Hz), 4.72 (2H, s), 6.92-6.98 (2H, m), 7.01-7.05 (1H, m), 7.18-7.29 (4H, m), 7.29-7.35 (2H, m), 7.45-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 112(1); Yield: 72.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.77 (2H, s), 6.84-6.92 (2H, m), 7.14 (1H, d, J=8.7 Hz), 7.29-7.43 (5H, m), 7.49 (1H, dd, J=2.4, 8.7 Hz), 7.68-7.77 (2H, m), 13.05 (1H, s).
A mixture of 2-chloro-6-fluorobenzaldehyde (634 mg, 4.00 mmol), 4-(trifluoromethoxy)phenylboronic acid (1.23 g, 6.00 mmol), palladium(II) acetate (9 mg, 0.04 mmol), 2-(di-tert-butylphosphino)biphenyl (23 mg, 0.08 mmol), potassium fluoride (697 mg, 12.00 mmol) and tetrahydrofuran (5 ml) was stirred at 80° C. for 5 hours. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate, and filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (893 mg, 79.0%) as a yellow oil.
1H-NMR (CDCl3) δ: 7.18-7.25 (2H, m), 7.29-7.32 (2H, m), 7.35-7.38 (2H, m), 7.56-7.64 (1H, m), 10.04 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 113(1) and 4-(tert-butyl)phenol; Yield: 73.5% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.94 (1H, dd, J=0.9, 8.4 Hz), 7.00-7.04 (3H, m), 7.24-7.28 (2H, m), 7.34-7.38 (2H, m), 7.39-7.42 (2H, m), 7.44-7.49 (1H, m), 10.34 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 113(2); Yield: 91.8% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 6.87-6.89 (2H, m), 7.00-7.03 (2H, m), 7.06-7.10 (1H, m), 7.27-7.30 (2H, m), 7.37-7.40 (2H, m), 7.66-7.69 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 113(3) and ethyl bromoacetate; Yield: 100.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.11 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.03 (2H, q, J=7.2 Hz), 4.50 (2H, s), 6.92-6.97 (3H, m), 7.08-7.10 (2H, m), 7.25-7.28 (2H, m), 7.34-7.36 (2H, m), 7.62-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 113(4); Yield: 81.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 4.50 (2H, s), 6.93-6.97 (3H, m), 7.15-7.17 (2H, m), 7.39-7.43 (4H, m), 7.65-7.70 (2H, m), 12.70 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 110(2) and ethyl 2-bromobutyrate; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=7.5 Hz), 1.20-1.33 (12H, m), 1.82-1.95 (2H, m), 4.10-4.26 (2H, m), 4.93 (1H, t, J=6.0 Hz), 6.90-6.95 (2H, m), 6.98 (1H, d, J=8.1 Hz), 7.20-7.26 (4H, m), 7.27-7.32 (2H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 114(1); Yield: 19.5% (white solid).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.5 Hz), 1.31 (9H, s), 1.95-2.04 (2H, m), 4.69 (1H, t, J=5.7 Hz), 6.95 (2H, d, J=8.4 Hz), 7.08 (1H, d, J=8.1 Hz), 7.18-7.29 (4H, m), 7.31-7.37 (2H, m), 7.48 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 102(1); Yield: 87.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.77-2.04 (4H, m), 2.69-2.74 (2H, m), 4.05-4.13 (2H, m), 5.65 (1H, brs), 6.88 (1H, d, J=8.1 Hz), 7.02 (1H, dd, J=2.1, 8.1 Hz), 7.15 (1H, d, J=2.1 Hz), 7.19-7.33 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 115(1) and ethyl bromoacetate; Yield: 97.1% (white solid).
1H-NMR (CDCl3) δ: 1.28 (3H, t, J=7.2 Hz), 1.82-1.90 (4H, m), 2.69-2.74 (2H, m), 4.05-4.09 (2H, m), 4.25 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.95 (1H, d, J=8.1 Hz), 7.11-7.32 (9H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 115(2); Yield: 78.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.73-1.76 (4H, m), 2.64-2.69 (2H, m), 4.01-4.08 (2H, m), 4.72 (2H, s), 7.06 (1H, d, J=8.4 Hz), 7.14-7.30 (7H, m), 7.39-7.42 (2H, m), 7.70-7.73 (2H, m), 12.93 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 115(1) and ethyl 2-bromoisobutyrate; Yield: 59.3% (yellow oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.56 (6H, s), 1.81-1.88 (4H, m), 2.70-2.76 (2H, m), 4.00-4.07 (2H, m), 4.23 (2H, q, J=7.2 Hz), 7.14-7.29 (8H, m), 7.48-7.51 (2H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 116(1); Yield: 26.5% (brown solid).
1H-NMR (DMSO-d6) δ: 1.38 (6H, s), 1.72-1.79 (4H, m), 2.67 (2H, t, J=6.9 Hz), 3.96 (2H, t, J=6.9 Hz), 6.92 (1H, d, J=8.1 Hz), 7.01 (1H, dd, J=2.1, 8.1 Hz), 7.15-7.31 (5H, m), 7.34 (1H, d, J=2.1 Hz), 7.37-7.40 (2H, m), 7.56-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 87(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 73.0% (brown oil).
1H-NMR (CDCl3) δ: 7.10-7.15 (1H, m), 7.25-7.31 (2H, m), 7.58-7.64 (4H, m), 9.96 (1H, s), 11.59 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 117(1) and 4-(tert-butyl)benzyl bromide; Yield: 100.0% (yellow solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 4.54 (2H, s), 6.93-7.01 (2H, m), 7.24-7.36 (5H, m), 7.59-7.63 (3H, m), 7.87 (1H, dd, J=2.1, 7.5 Hz), 10.39 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 117(2); Yield: 95.7% (yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 4.43 (2H, s), 6.88 (1H, dd, J=2.1, 7.8 Hz), 6.98 (1H, dd, J=2.1, 7.8 Hz), 7.04-7.12 (3H, m), 7.28-7.35 (4H, m), 7.63-7.66 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 117(3) and ethyl bromoacetate; Yield: 74.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.26-1.33 (12H, m), 4.29 (2H, q, J=7.2 Hz), 4.74 (2H, s), 4.79 (2H, s), 6.90 (1H, dd, J=1.8, 7.8 Hz), 6.93-7.00 (3H, m), 7.07-7.12 (1H, m), 7.17-7.23 (4H, m), 7.44-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 117(4); Yield: 87.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 4.80 (2H, s), 4.83 (2H, s), 6.92 (1H, dd, J=1.5, 7.8 Hz), 6.95-6.98 (2H, m), 7.03 (1H, dd, J=1.5, 7.8 Hz), 7.10-7.14 (1H, m), 7.18-7.20 (2H, m), 7.33-7.36 (2H, m), 7.46-7.49 (2H, m), 13.90 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 117(3) and ethyl 2-bromoisobutyrate; Yield: 44.9% (yellow oil).
1H-NMR (CDCl3) δ: 1.25-1.33 (12H, m), 1.67 (6H, s), 4.26 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.88 (1H, dd, J=1.8, 7.8 Hz), 6.92-6.99 (3H, m), 7.00-7.12 (1H, m), 7.16-7.24 (4H, m), 7.44-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 118(1); Yield: 12.3% (yellow solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 1.65 (6H, s), 4.61 (2H, s), 6.88-6.92 (2H, m), 7.03-7.16 (3H, m), 7.22-7.26 (4H, m), 7.49-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 110(2) and ethyl bromofluoroacetate; Yield: 98.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.22-1.28 (3H, m), 1.31 (9H, s), 4.25 (2H, q, J=7.2 Hz), 5.98 (1H, d, J=59.1 Hz), 6.92-6.96 (2H, m), 7.20-7.37 (7H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 119(1); Yield: 90.7% (yellow oil).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 6.36 (1H, d, J=59.1 Hz), 6.90-6.93 (2H, m), 7.35-7.47 (6H, m), 7.54 (1H, dd, J=1.8, 8.4 Hz), 7.71-7.74 (2H, m), 14.09 (1H, brs).
Sodium hydride (65 mg, 1.490 mmol) was added to a mixture of the intermediate 110(2) (300 mg, 0.745 mmol), chlorodifluoroacetic acid (117 mg, 0.894 mmol) and dioxane (10 ml) at 0° C., and the mixture was refluxed for 10 hours. The reaction mixture was cooled to room temperature, diluted with water, acidified by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (95 mg, 25.7%) as a white solid.
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 6.91-6.95 (2H, m), 7.26 (1H, d, J=1.5 Hz), 7.34-7.46 (6H, m), 7.69-7.71 (2H, m).
A mixture of lithium hydroxide (101 mg, 2.40 mmol), diethyl cyanomethylphosphonate (390 mg, 2.20 mmol) and tetrahydrofuran (20 ml) was stirred at 70° C. for 30 minutes under argon atmosphere. After the reaction mixture was cooled to room temperature, the intermediate 4(2) (857 mg, 2.00 mmol) was added, and the mixture was stirred at room temperature for 4 hours. 1 N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (631 mg, 70.0%) as a colorless oil.
This compound was obtained as a mixture of the rotational isomers.
Major isomer (E form): 1H-NMR (CDCl3) δ: 1.35 (9H, s), 5.14 (2H, s), 6.13 (1H, d, J=16.8 Hz), 7.07-7.76 (12H, m).
Minor isomer (Z form): 1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.12 (2H, s), 5.46 (1H, d, J=12.0 Hz), 7.06-7.75 (11H, m), 8.34 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 121(1); Yield: 46% (white solid).
1H-NMR (CDCl3) δ: 2.72 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 5.23 (1H, s), 6.82 (1H, d, J=8.1 Hz), 7.22-7.28 (2H, m), 7.32 (1H, dd, J=2.1, 8.1 Hz), 7.36 (1H, d, J=2.1 Hz), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 121(2) and 4-(tert-butyl)benzyl bromide; Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 2.68 (2H, t, J=7.2 Hz), 3.06 (2H, t, J=7.2 Hz), 5.10 (2H, s), 7.03 (1H, d, J=8.4 Hz), 7.24-7.28 (2H, m), 7.33-7.38 (2H, m), 7.39-7.46 (4H, m), 7.52-7.57 (2H, m).
A mixture of the intermediate 121(3) (227 mg, 0.5 mmol), sodium azide (98 mg, 1.5 mmol), triethylamine hydrochloride (103 mg, 0.75 mol) and 1-methyl-2-pyrrolidone (5 mL) was stirred at 150° C. for 4 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (45 mg, 18%) as a white solid.
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 3.10-3.27 (4H, m), 5.16 (2H, s), 7.15 (1H, d, J=8.7 Hz), 7.39-7.45 (6H, m), 7.44 (1H, d, J=2.4 Hz), 7.50 (1H, dd, J=2.4, 8.7 Hz), 7.65-7.70 (2H, m).
A mixture of the intermediate 105(1) (110 mg, 0.264 mmol), bromoacetonitrile (34 mg, 0.291 mmol), cesium carbonate (95 mg, 0.291 mmol) and acetone (2 ml) was stirred at room temperature for 2 hours. Water was added to the residue obtained by evaporation of the solvent under reduced pressure, and the residue was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (90 mg, 74.8%) as a white solid.
1H-NMR (CDCl3) δ: 1.34 (9H, s), 4.88 (2H, s), 5.14 (2H, s), 7.09 (1H, d, J=7.8 Hz), 7.25-7.30 (4H, m), 7.36-7.45 (4H, m), 7.51-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 121(4) using the following starting material.
Starting material: the intermediate 122(1); Yield: 81.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 5.13 (2H, s), 5.59 (2H, s), 7.15-7.20 (1H, m), 7.26-7.31 (1H, m), 7.34-7.47 (7H, m), 7.72-7.77 (2H, m).
A mixture of 3,5-dimethylbenzyl bromide (1.59 g, 7.986 mmol), 4-bromoaniline (1.374 g, 7.986 mmol), potassium carbonate (5.519 g, 39.93 mmol) and N,N-dimethylformamide (6.5 ml) was stirred at 80° C. for 2 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15) to give the title compound (2.106 g, 57.2%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 2.30 (6H, s), 4.00 (1H, brs), 4.20 (2H, s), 6.47-6.53 (2H, m), 6.90-6.98 (3H, m), 7.21-7.26 (2H, m).
Methyl chloroglyoxylate (0.566 ml, 6.16 mmol) was added dropwise to a mixture of the intermediate 123(1) (1.49 g, 5.13 mmol), triethylamine (1.08 ml, 7.70 mmol) and dichloromethane (20 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (1.66 g, 86%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 2.26 (6H, s), 3.59 (3H, s), 4.84 (2H, s), 6.80 (2H, s), 6.90 (1H, s), 6.70-6.92 (2H, m), 7.40-7.46 (2H, m).
A mixture of the intermediate 123(2) (707 mg, 1.88 mmol), 4-(trifluoromethoxy)phenylboronic acid (500 mg, 2.44 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (300 mg, 0.357 mmol), potassium carbonate (389 mg, 2.82 mmol), dioxane (10 ml) and water (1 ml) was stirred at 80° C. for 4 hours. The reaction mixture was cooled to room temperature, and filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (630 mg, 73%) as a pale brown oil.
1H-NMR (CDCl3) δ: 2.26 (6H, s), 3.59 (3H, s), 4.90 (2H, s), 6.85 (2H, s), 6.91 (1H, s), 7.12-7.17 (2H, m), 7.25-7.31 (2H, m), 7.46-7.52 (2H, m), 7.53-7.59 (2H, m).
A mixture of the intermediate 123(3) (200 mg, 0.437 mmol), a 2 N aqueous solution of sodium hydroxide (2 ml) and water (1 ml) was irradiated with ultrasound for 5 minutes. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (130 mg, 66%) as a white solid.
1H-NMR (DMSO-d6) δ: 2.20 (6H, s), 4.87 (2H, s), 6.78-7.00 (3H, m), 7.30-7.37 (2H, m), 7.39-7.45 (2H, m), 7.51-7.59 (2H, m), 7.70-7.77 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-chlorobenzyl chloride and 4-bromoaniline; Yield: 21% (white solid).
1H-NMR (CDCl3) δ: 4.10 (1H, brs), 4.25-4.31 (2H, m), 6.44-6.51 (2H, m), 7.20-7.34 (6H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 124(1) and methyl chloroglyoxylate; Yield: 96% (colorless oil).
1H-NMR (CDCl3) δ: 3.59 (3H, s), 4.88 (2H, s), 6.88-6.94 (2H, m), 7.12-7.17 (2H, m), 7.24-7.30 (2H, m), 7.42-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 124(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 28% (pale brown oil).
1H-NMR (CDCl3) δ: 3.59 (3H, s), 4.94 (2H, s), 7.09-7.22 (4H, m), 7.24-7.32 (4H, m), 7.47-7.59 (4H, m).
The title compound was obtained in the same manner as the Example 123(4) using the following starting material.
Starting material: the intermediate 124(3); Yield: 93% (white solid).
1H-NMR (DMSO-d6) δ: 4.91 (2H, s), 7.20-7.38 (6H, m), 7.38-7.48 (2H, m), 7.52-7.63 (2H, m), 7.71-7.82 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 4-bromonitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 7.32-7.38 (2H, m), 7.62-7.68 (2H, m), 7.69-7.75 (2H, m), 8.29-8.35 (2H, m).
A mixture of the intermediate 125(1) (6.41 g, 22.6 mmol), 10% platinum on activated carbon (150 mg) and methanol (50 ml) was stirred for 16 hours under hydrogen atmosphere. The reaction mixture was filtered through Celite. The filtrate was concentrated under reduced pressure to give the title compound (5.48 g, 96%) as a white solid.
1H-NMR (CDCl3) δ: 3.75 (2H, brs), 6.73-6.78 (2H, m), 7.23 (2H, d, J=8.4 Hz), 7.35-7.40 (2H, m), 7.50-7.55 (2H, m).
A solution of methyl chloroglyoxylate (2.98 ml, 32.4 mmol) in dichloromethane (10 ml) was added dropwise at a slow speed to a mixture of the intermediate 125(2) (5.476 g, 21.6 mmol), sodium hydrogen carbonate (3.62 g, 43.2 mmol), dichloromethane (40 ml) and water (40 ml), and stirred at 0° C. for 2 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (6.71 g, 91.5%) as a white solid.
1H-NMR (DMSO-d6) δ: 3.87 (3H, s), 7.41-7.48 (2H, m), 7.67-7.73 (2H, m), 7.76-7.82 (2H, m), 7.84-7.91 (2H, m), 10.94 (1H, s).
A mixture of the intermediate 125(3) (250 mg, 0.737 mmol), 3-methylbenzyl bromide (0.299 ml, 2.21 mmol), potassium carbonate (306 mg, 2.21 mmol), 18-crown-6 (20 mg, 0.074 mmol) and acetonitrile (10 ml) was stirred at 50° C. for 3 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (320 mg, 98%) as a colorless oil.
1H-NMR (CDCl3) δ: 2.32 (3H, s), 3.59 (3H, s), 4.95 (2H, s), 7.02-7.32 (8H, m), 7.46-7.52 (2H, m), 7.52-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 123(4) using the following starting material.
Starting material: the intermediate 125(4); Yield: 93% (white solid).
1H-NMR (DMSO-d6) δ: 2.25 (3H, s), 4.92 (2H, s), 6.95-7.23 (4H, m), 7.30-7.38 (2H, m), 7.39-7.44 (2H, m), 7.52-7.60 (2H, m), 7.70-7.77 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: 4-bromoaniline and methyl chloroglyoxylate; Yield: 68.9% (white solid).
1H-NMR (CDCl3) δ: 3.98 (3H, s), 7.47-7.57 (4H, m), 8.85 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-(tert-butyl)benzyl bromide; Yield: 99.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.58 (3H, s), 4.88 (2H, s), 6.93 (2H, d, J=8.1 Hz), 7.12 (2H, d, J=8.1 Hz), 7.30 (2H, d, J=8.1 Hz), 7.43 (2H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-methoxyphenylboronic acid; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, m), 3.57 (3H, s), 3.84 (3H, s), 4.93 (2H, s), 6.96 (2H, d, J=9.0 Hz), 7.01 (2H, d, J=8.4 Hz), 7.18 (2H, d, J=8.7 Hz), 7.31 (2H, d, J=8.4 Hz), 7.46-7.52 (4H, m).
A mixture of the intermediate 126(3) (230 mg, 0.533 mmol), methanol (1.5 ml), a 2 N aqueous solution of sodium hydroxide (0.8 ml) and tetrahydrofuran (1.5 ml) was stirred at room temperature for 10 minutes. The reaction mixture was adjusted to pH 5-6 by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (160 mg, 71.9%) as a white solid.
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 3.79 (3H, s), 4.93 (2H, s), 7.01 (2H, d, J=8.7 Hz), 7.16 (2H, d, J=8.4 Hz), 7.27 (2H, d, J=8.7 Hz), 7.35 (2H, d, J=8.4 Hz), 7.59-7.65 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-fluorophenylboronic acid. Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.58 (3H, s), 4.94 (2H, s), 7.09-7.19 (6H, m), 7.31 (2H, d, J=7.8 Hz), 7.47-7.54 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 127(1); Yield: 71.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 4.95 (2H, s), 7.16 (2H, d, J=8.4 Hz), 7.25-7.36 (6H, m), 7.66-7.73 (4H, m).
A mixture of the intermediate 125(2) (112 mg, 0.442 mmol), 4-(tert-butyl)phenylboronic acid (87 mg, 0.486 mmol), copper(II) acetate (40 mg, 0.221 mmol), triethylamine (0.061 ml, 0.884 mmol) and pyridine (3.0 ml) was stirred at 50° C. for 2 hours. The reaction mixture was cooled to room temperature and filtered through Celite. The filtrate was diluted with 1 N hydrochloric acid (10 ml), and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (50 mg, 29%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.73 (1H, s), 7.05-7.12 (4H, m), 7.22-7.27 (2H, m), 7.29-7.36 (2H, m), 7.41-7.47 (2H, m), 7.52-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 128(1) and methyl chloroglyoxylate; Yield: 88% (pale yellow oil).
This compound was obtained as a mixture of the rotational isomers (3:2).
Major isomer: 1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.60 (3H, s), 7.20-7.46 (8H, m), 7.51-7.62 (4H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.65 (3H, s), 7.20-7.46 (8H, m), 7.51-7.62 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 128(2); Yield: 96% (pale brown solid).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (DMSO-d6) δ: 1.25-1.31 (9H, m), 7.06-7.55 (8H, m), 7.66-7.86 (4H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-(tert-butyl)benzyl bromide; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.58 (3H, s), 4.95 (2H, s), 7.14-7.20 (4H, m), 7.25-7.34 (4H, m), 7.48-7.59 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 129(1); Yield: 86.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.91 (2H, s), 7.15-7.60 (8H, m), 7.57 (2H, d, J=8.4 Hz), 7.73 (2H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 3-bromoaniline and 4-(tert-butyl)benzyl bromide; Yield: 66.4% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.04 (1H, brs), 4.25 (2H, d, J=4.8 Hz), 6.51-6.55 (1H, m), 6.78 (1H, t, J=1.8 Hz), 6.80-6.83 (1H, m), 7.00 (1H, t, J=8.1 Hz), 7.28 (2H, d, J=8.4 Hz), 7.36-7.39 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 130(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 86.7% (yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.12 (2H, d, J=7.2 Hz), 4.34 (1H, s), 6.63-6.67 (1H, m), 6.80-6.81 (1H, m), 6.87-6.91 (1H, m), 7.22-7.29 (3H, m), 7.33 (2H, d, J=8.1 Hz), 7.39 (2H, d, J=8.1 Hz), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 130(2) and methyl chloroglyoxylate; Yield: 87.5% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.55 (3H, s), 4.95 (2H, s), 7.11-7.13 (2H, m), 7.17 (2H, d, J=8.1 Hz), 7.25 (2H, d, J=8.1 Hz), 7.31-7.34 (2H, m), 7.38-7.44 (3H, m), 7.48-7.52 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: methyl the intermediate 130(3); Yield: 32.3% (white solid).
1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.95 (2H, s), 7.16 (2H, d, J=7.8 Hz), 7.26-7.33 (3H, m), 7.38-7.43 (3H, m), 7.51-7.53 (2H, m), 7.68 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-methoxybenzyl bromide; Yield: 82.7% (colorless oil).
1H-NMR (CDCl3) δ: 3.57 (3H, s), 3.79 (3H, s), 4.91 (2H, s), 6.82 (2H, d, J=8.4 Hz), 7.11 (2H, d, J=8.4 Hz), 7.16 (2H, d, J=8.7 Hz), 7.28 (2H, d, J=8.4 Hz), 7.49 (2H, d, J=8.4 Hz), 7.56 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 131(1); Yield: 55.8% (white solid).
1H-NMR (DMSO-d6) δ: 3.69 (3H, s), 4.87 (2H, s), 6.80-6.89 (2H, m), 7.10-7.38 (4H, m), 7.42 (2H, d, J=8.4 Hz), 7.55 (2H, d, J=8.4 Hz), 7.74 (2H, d, J=8.4 Hz).
A mixture of 4-(trifluoromethoxy)phenol (2.50 g, 14.036 mmol), 4-fluoro-1-nitrobenzene (1.98 g, 14.036 mmol), potassium carbonate (2.90 g, 20.982 mmol) and N,N-dimethylacetamide (15 ml) was stirred at 160° C. for 2 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (4.18 g, 100%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 7.02-7.06 (2H, m), 7.10-7.14 (2H, m), 7.26-7.31 (2H, m), 8.21-8.25 (2H, m).
A mixture of the intermediate 132(1) (4.18 g, 13.970 mmol), 10% platinum on activated carbon (270 mg) and ethanol (40 ml) was stirred for 3 hours under hydrogen atmosphere. The reaction mixture was filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (3.54 g, 93.9%) as a yellow oil.
1H-NMR (CDCl3) δ: 3.61 (2H, s), 6.67-6.70 (2H, m), 6.85-6.88 (2H, m), 6.89-6.92 (2H, m), 7.12 (2H, t, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 132(2) and methyl chloroglyoxylate; Yield: 96.9% (white solid).
1H-NMR (CDCl3) δ: 3.98 (3H, s), 6.97-7.05 (4H, m), 7.16-7.22 (2H, m), 7.62-7.65 (2H, m), 8.85 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 132(3) and 4-(tert-butyl)benzyl bromide; Yield: 92.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.59 (3H, s), 4.88 (2H, s), 6.88-6.91 (2H, m), 6.98-7.01 (2H, m), 7.03-7.06 (2H, m), 7.16 (2H, d, J=8.4 Hz), 7.20 (2H, d, J=8.4 Hz), 7.30-7.33 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 132(4); Yield: 78.5% (yellow solid).
1H-NMR (CDCl3) δ: 1.23 (9H, s), 4.80 (2H, s), 5.83 (1H, brs), 6.75 (2H, d, J=8.4 Hz), 6.89-6.97 (4H, m), 7.08-7.13 (4H, m), 7.23 (2H, d, J=7.2 Hz).
The title compound was obtained in the same manner as the Example 123(4) using the following starting material.
Starting material: the intermediate 129(1); Yield: 56.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.89 (2H, s), 7.18-7.43 (8H, m), 7.54-7.57 (2H, m), 7.72-7.77 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-(methylsulfanyl)phenylboronic acid; Yield: 81.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.52 (3H, s), 3.58 (3H, s), 4.94 (2H, s), 7.11-7.38 (4H, m), 7.28-7.36 (4H, m), 7.45-7.54 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 134(1); Yield: 94.2% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.51 (3H, s), 4.93 (2H, s), 7.13-7.18 (2H, m), 7.28-7.36 (6H, m), 7.58-7.66 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-chlorophenylboronic acid; Yield: 88.0% (pale brown oil).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 3.59 (2H, s), 4.94 (2H, s), 7.09-7.54 (12H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 135(1); Yield: 44.0% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.89 (2H, s), 7.02-7.74 (12H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 5-bromo-2-methylaniline and 4-(tert-butyl)benzyl bromide; Yield: 71.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.08 (3H, s), 3.81 (1H, brs), 4.28 (2H, d, J=4.8 Hz), 6.75-6.92 (2H, m), 6.88-6.92 (1H, m), 7.28-7.32 (2H, m), 4.28 (2H, d, J=4.8 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 136(1) and methyl chloroglyoxylate; Yield: 94.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.07 (3H, s), 3.54 (3H, s), 4.35 (1H, d, J=13.8 Hz), 5.20 (1H, d, J=13.8 Hz), 6.91 (1H, d, J=2.1 Hz), 7.07-7.13 (3H, m), 7.28-7.33 (2H, m), 7.35 (1H, dd, J=2.1, 8.4 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 136(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 80.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.27 (3H, s), 3.48 (3H, s), 4.14 (1H, d, J=13.5 Hz), 5.51 (1H, d, J=13.5 Hz), 6.75 (1H, d, J=1.8 Hz), 7.11-7.20 (4H, m), 7.24-7.34 (5H, m), 7.42 (1H, dd, J=1.8, 7.8 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 136(3); Yield: 37.0% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.19 (3H, s), 4.32 (1H, d, J=14.1 Hz), 5.26 (1H, d, J=14.1 Hz), 6.93 (1H, d, J=1.8 Hz), 7.07-7.20 (2H, m), 7.29-7.50 (7H, m), 6.93 (1H, dd, J=1.8, 10.2 Hz).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 1.97 (3H, s), 4.60 (1H, d, J=14.1 Hz), 4.96 (1H, d, J=14.1 Hz), 6.80-7.60 (11H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 136(2) and phenylboronic acid; Yield: 98.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.26 (3H, s), 3.47 (3H, s), 4.17 (1H, d, J=13.8 Hz), 5.49 (1H, d, J=13.8 Hz), 6.81 (1H, d, J=1.8 Hz), 7.13-7.17 (2H, m), 7.23-7.38 (8H, m), 7.45 (1H, dd, J=1.8, 7.5 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 137(1); Yield: 44.3% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.22 (3H, s), 4.23 (1H, d, J=14.4 Hz), 5.33 (1H, d, J=14.4 Hz), 6.85 (1H, d, J=1.8 Hz), 7.12-7.16 (2H, m), 7.28-7.41 (8H, m), 7.54 (1H, dd, J=1.8, 8.1 Hz).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.00 (3H, s), 4.55 (1H, d, J=15.0 Hz), 4.97 (1H, d, J=15.0 Hz), 6.73-7.60 (12H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 136(2) and 3-nitrophenylboronic acid; Yield: 52.1% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.28 (3H, s), 3.51 (3H, s), 4.20 (1H, d, J=14.1 Hz), 5.49 (1H, d, J=14.1 Hz), 6.89 (1H, d, J=2.1 Hz), 7.11-7.21 (2H, m), 7.29-7.42 (3H, m), 7.45-7.55 (3H, m), 8.13-8.26 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 138(1); Yield: 96.5% (pale white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.26 (3H, s), 3.99 (1H, d, J=13.8 Hz), 5.29 (1H, d, J=13.8 Hz), 7.01 (1H, d, J=1.8 Hz), 7.12-8.24 (10H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 3.31 (3H, s), 4.54 (1H, d, J=15.3 Hz), 4.98 (1H, d, J=15.3 Hz), 7.08 (1H, d, J=1.8 Hz), 7.10-8.24 (10H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 3-bromo-5-(trifluoromethyl)aniline and 4-(tert-butyl)benzyl bromide; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.27 (2H, s), 4.59 (1H, s), 6.73-6.75 (1H, m), 6.87-6.89 (1H, m), 7.03-7.05 (1H, m), 7.23-7.28 (2H, m), 7.36-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 139(1) and methyl chloroglyoxylate; Yield: 65.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.63 (3H, s), 4.92 (2H, s), 7.09-7.18 (3H, m), 7.30-7.36 (2H, m), 7.39-7.42 (1H, m), 7.69-7.71 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 139(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 75.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.59 (3H, s), 4.97 (2H, s), 7.13-7.17 (2H, m), 7.26-7.45 (8H, m), 7.72-7.74 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 139(3); Yield: 43.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.97 (2H, s), 7.10-7.22 (2H, m), 7.29 (1H, d, J=8.4 Hz), 7.46 (2H, d, J=8.7 Hz), 7.57-7.61 (2H, m), 7.72-7.90 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 139(2) and phenylboronic acid; Yield: 91.1% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.58 (3H, s), 4.97 (2H, s), 7.13-7.18 (2H, m), 7.26-7.46 (9H, m), 7.75-7.77 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 140(1); Yield: 24.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.97 (2H, s), 7.10-7.24 (2H, m), 7.30 (2H, d, J=7.8 Hz), 7.38-7.51 (3H, m), 7.53-7.64 (3H, m), 7.69-7.73 (1H, m), 7.74-7.82 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-methylphenylboronic acid; Yield: 91.3% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.39 (3H, s), 3.57 (3H, s), 4.93 (2H, s), 7.05-7.38 (8H, m), 7.38-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 141(1); Yield: 99.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.32 (3H, s), 4.87 (2H, s), 7.06-7.45 (8H, m), 7.51 (4H, d, J=8.0 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 3-nitrophenylboronic acid; Yield: 59.3% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.61 (3H, s), 4.96 (2H, s), 7.13-7.25 (4H, m), 7.29-7.39 (2H, m), 7.54-7.68 (3H, m), 7.84-7.94 (1H, m), 8.18-8.27 (1H, m), 8.38-8.46 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 142(1); Yield: 99.9% (yellow solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.91 (2H, s), 7.09-7.27 (2H, m), 7.29 (2H, d, J=8.2 Hz), 7.43 (2H, d, J=8.5 Hz), 7.67 (2H, d, J=8.5 Hz), 7.73 (1H, t, J=8.2 Hz), 8.06-8.22 (2H, m) 8.36-8.44 (1H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-methylbenzyl chloride; Yield: 24.1% (white solid).
1H-NMR (CDCl3) δ: 2.31 (3H, s), 3.57 (3H, s), 4.94 (2H, s), 7.06-7.17 (6H, m), 7.27 (2H, d, J=8.8 Hz), 7.49 (2H, d, J=8.8 Hz), 7.55 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 143(1): Yield: 86.9% (white solid).
1H-NMR (DMSO-d6) δ: 2.23 (3H, s), 4.88 (2H, s), 6.98-7.48 (8H, m), 7.48-7.63 (2H, m) 7.73 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 2,4-dichlorobenzyl chloride; Yield: 59.5% (colorless oil).
1H-NMR (CDCl3) δ: 3.61 (3H, s), 5.11 (2H, s), 7.14-7.42 (7H, m), 7.51 (2H, d, J=8.8 Hz), 7.56 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 144(1); Yield: 98.8% (white solid).
1H-NMR (DMSO-d6) δ: 4.94 (2H, s), 7.33-7.48 (6H, m), 7.53-7.63 (3H, m), 7.75 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-(trifluoromethyl)phenylboronic acid; Yield: 55.7% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.60 (3H, s), 4.95 (2H, s), 7.18 (4H, d, J=8.1 Hz), 7.32 (2H, d, J=8.1 Hz), 7.55 (2H, d, J=8.7 Hz), 7.62-7.76 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 145(1); Yield: 99.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.90 (2H, s), 7.09-7.36 (4H, m), 7.41 (2H, d, J=8.5 Hz), 7.63 (2H, d, J=8.5 Hz), 7.78 (2H, d, J=8.5 Hz), 7.85 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromo-2-methylaniline and 4-(tert-butyl)benzyl bromide; Yield: 55.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.33 (9H, s), 2.12 (3H, s), 3.82 (1H, brs), 4.30 (2H, s), 6.49 (1H, d, J=9.3 Hz), 7.12-7.21 (2H, m), 7.23-7.33 (2H, m), 7.34-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 146(1) and methyl chloroglyoxylate; Yield: 80.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.13 (3H, s), 3.52 (3H, s), 4.26 (1H, d, J=14.0 Hz), 5.24 (1H, d, J=14.0 Hz), 6.64 (1H, d, J=8.5 Hz), 7.04-7.15 (2H, m), 7.15-7.23 (1H, m), 7.23-7.34 (2H, m), 7.34-7.44 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 146(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 66.9% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.23 (3H, s), 3.52 (3H, s), 4.33 (1H, d, J=14.1 Hz), 5.29 (1H, d, J=14.1 Hz), 6.78-6.86 (1H, m), 6.88 (1H, d, J=8.2 Hz), 7.09 (1H, d, J=8.8 Hz), 7.16 (2H, d, J=8.2 Hz), 7.20-7.36 (3H, m), 7.42 (1H, s), 7.52-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 146(3); Yield: 41.1% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.24 (3H, s), 4.10 (1H, d, J=13.8 Hz), 5.13 (1H, d, J=13.8 Hz), 6.94 (1H, d, J=8.2 Hz), 7.14 (1H, d, J=8.0 Hz), 7.21-7.56 (7H, m), 7.75 (2H, d, J=8.8 Hz).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 1.98 (3H, s), 4.48-4.74 (1H, m), 4.74-4.98 (1H, m), 6.90-7.86 (11H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromo-2-chloroaniline and 4-(tert-butyl)benzyl bromide; Yield: 43.7% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.33 (2H, s), 4.70 (1H, brs), 6.52 (1H, d, J=8.8 Hz), 7.18 (1H, d, J=2.2, 8.8 Hz), 7.27 (2H, d, J=8.0 Hz), 7.34-7.43 (3H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 147(1) and methyl chloroglyoxylate; Yield: 88.3% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.59 (3H, s), 4.17 (1H, d, J=14.4 Hz), 5.51 (1H, d, J=14.4 Hz), 6.71 (1H, d, J=8.5 Hz), 7.06-7.18 (2H, m), 7.21-7.36 (3H, m), 7.63 (1H, d, J=2.2 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 147(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 43.9% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.59 (3H, s), 4.25 (1H, d, J=14.4 Hz), 5.56 (1H, d, J=14.4 Hz), 6.95 (1H, d, J=7.8 Hz), 7.17 (2H, d, J=8.1 Hz), 7.24-7.37 (5H, m), 7.51-7.60 (2H, m), 7.66 (1H, d, J=1.8 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 147(3); Yield: 92.1% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.06 (1H, d, J=14.7 Hz), 5.39 (1H, d, J=14.7 Hz), 7.08-7.22 (2H, m), 7.22-7.39 (3H, m), 7.39-7.58 (3H, m), 7.74-7.88 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.38-4.84 (1H, m), 4.84-5.28 (1H, m), 7.02-7.88 (11H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 2-bromoaniline and methyl chloroglyoxylate; Yield: 98.5% (white solid).
1H-NMR (CDCl3) δ: 4.00 (3H, s), 7.04-7.61 (3H, m), 8.41-8.44 (1H, m), 9.48 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: methyl N-(2-bromophenyl)oxamate and 4-(tert-butyl)benzyl bromide; Yield: 25.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 4.18 (1H, d, J=14.1 Hz), 5.56 (1H, d, J=14.1 Hz), 6.82-6.86 (1H, m), 7.11-7.30 (6H, m), 7.63-7.67 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 148(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 80.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (9H, s), 3.47 (1H, d, J=14.1 Hz), 3.63 (3H, s), 5.10 (1H, d, J=14.1 Hz), 6.82-6.86 (1H, m), 6.91-6.95 (2H, m), 7.17-7.42 (7H, m), 7.59-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 148(3); Yield: 66.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.20 (9H, s), 3.14 (1H, d, J=14.7 Hz), 4.82 (1H, d, J=14.7 Hz), 6.86 (2H, d, J=8.1 Hz), 7.05-7.36 (6H, m), 7.43 (2H, d, J=8.4 Hz), 8.05 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 4-(4-aminophenyl)benzonitrile and methyl chloroglyoxylate; Yield: 80.9% (white solid).
1H-NMR (DMSO-d6) δ: 3.87 (3H, s), 7.77-7.94 (8H, m), 10.98 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 149(1) and 4-(tert-butyl)benzyl bromide; Yield: 77.7% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.60 (3H, s), 4.95 (2H, s), 7.15-7.22 (4H, m), 7.32 (2H, d, J=8.4 Hz), 7.54 (2H, d, J=8.1 Hz), 7.65 (2H, d, J=7.8 Hz), 7.73 (2H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 149(2); Yield: 48.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.91 (2H, s), 7.12-7.34 (4H, m), 7.42 (2H, d, J=8.7 Hz), 7.64 (2H, d, J=8.7 Hz), 7.82-7.92 (4H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 4-bromo-2-(trifluoromethyl)aniline and methyl chloroglyoxylate; Yield: 71.9% (white solid).
1H-NMR (CDCl3) δ: 4.00 (3H, s), 7.73 (1H, dd, J=2.1, 8.7 Hz), 7.79 (1H, d, J=2.1 Hz), 8.29 (1H, d, J=8.7 Hz), 9.30 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 150(1) and 4-(tert-butyl)benzyl bromide; Yield: 70.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.61 (3H, s), 3.91 (1H, d, J=14.7 Hz), 5.76 (1H, d, J=14.7 Hz), 6.66 (1H, d, J=8.7 Hz), 7.12-7.17 (2H, m), 7.29-7.36 (2H, m), 7.52 (1H, dd, J=2.4, 8.7 Hz), 7.86 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 150(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 44.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.60 (3H, s), 3.99 (1H, d, J=14.4 Hz), 5.79 (1H, d, J=14.4 Hz), 6.91 (1H, d, J=8.4 Hz), 7.16-7.21 (2H, m), 7.27-7.36 (4H, m), 7.54-7.63 (3H, m), 7.90 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 150(3); Yield: 66.7% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 3.86 (1H, d, J=14.7 Hz), 5.51 (1H, d, J=14.7 Hz), 7.08-7.80 (11H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 4.26 (1H, d, J=15.3 Hz), 5.33 (1H, d, J=15.3 Hz), 6.79 (1H, d, J=8.4 Hz), 7.08-7.80 (10H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 4-bromo-2-(trifluoromethoxy)aniline and methyl chloroglyoxylate; Yield: 80.7% (white solid).
1H-NMR (CDCl3) δ: 4.00 (3H, s), 7.47-7.50 (2H, m), 8.36-8.41 (1H, m), 9.21 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 151(1) and 4-(tert-butyl)benzyl bromide; Yield: 89.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.61 (3H, s), 4.31 (1H, d, J=14.7 Hz), 5.37 (1H, d, J=14.7 Hz), 6.84 (1H, d, J=8.7 Hz), 7.08-7.13 (2H, m), 7.25-7.32 (3H, m), 7.43-7.46 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 151(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 44.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.61 (3H, s), 4.37 (1H, d, J=14.4 Hz), 5.44 (1H, d, J=14.4 Hz), 7.06 (1H, d, J=8.1 Hz), 7.14-7.17 (2H, m), 7.26-7.35 (5H, m), 7.43-7.48 (1H, m), 7.53-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 151(3); Yield: 47.6% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.84 (2H, s), 7.07-7.80 (11H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.77 (2H, s), 7.07-7.80 (11H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 4-bromo-2,6-dimethylaniline and methyl chloroglyoxylate; Yield: 73.0% (white solid).
1H-NMR (CDCl3) δ: 2.22 (6H, s), 3.99 (3H, s), 7.26 (2H, d, J=1.5 Hz), 8.32 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 152(1) and 4-(tert-butyl)benzyl bromide; Yield: 89.1% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 1.88 (6H, s), 3.51 (3H, s), 4.72 (2H, s), 7.11-7.15 (2H, m), 7.16-7.18 (2H, m), 7.25-7.30 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 152(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 79.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 1.97 (6H, s), 3.51 (3H, s), 4.78 (2H, s), 7.16-7.22 (4H, m), 7.25-7.30 (4H, m), 7.55-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 152(3); Yield: 51.7% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 1.99 (6H, s), 4.55 (2H, s), 7.13-7.77 (10H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 1.85 (6H, s), 4.62 (2H, s), 7.13-7.77 (10H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenol; Yield: 94% (yellow oil).
1H-NMR (CDCl3) δ: 7.02-7.09 (3H, m), 7.20-7.30 (3H, m), 7.52-7.60 (1H, m), 7.98 (1H, dd, J=1.5, 8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 153(1); Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 3.78 (2H, brs), 6.70-6.78 (1H, m), 6.84 (1H, dd, J=1.8, 8.1 Hz), 6.88 (1H, dd, J=1.5, 8.1 Hz), 6.93-6.99 (2H, m), 7.01 (1H, dt, J=1.5, 8.1 Hz), 7.12-7.18 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 153(2) and methyl chloroglyoxylate; Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 3.96 (3H, s), 6.89 (1H, dd, J=1.8, 8.1 Hz), 7.03-7.26 (6H, m), 8.79 (1H, dd, J=1.8, 7.8 Hz), 9.43 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 153(3) and 4-(tert-butyl)benzyl bromide; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.62 (3H, s), 4.72 (1H, d, J=14.4 Hz), 5.13 (1H, d, J=14.4 Hz), 6.78 (1H, dd, J=1.5, 8.4 Hz), 6.85-6.93 (2H, m), 6.97-7.10 (2H, m), 7.12-7.28 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 153(4); Yield: 84% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.64 (1H, d, J=15.0 Hz), 5.03 (1H, d, J=15.0 Hz), 6.80-6.86 (1H, m), 6.98-7.04 (2H, m), 7.06-7.36 (7H, m), 7.37-7.44 (2H, m), 13.95 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 132(3) and benzyl bromide; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 4.92 (2H, s), 6.85-6.92 (2H, m), 6.96-7.05 (4H, m), 7.17-7.35 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 154(1); Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 4.89 (2H, s), 5.71 (1H, brs), 6.82-7.02 (6H, m), 7.14-7.23 (4H, m), 7.24-7.31 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-fluorobenzyl chloride; Yield: 67.6% (colorless oil).
1H-NMR (CDCl3) δ: 3.59 (3H, s), 4.94 (2H, s), 6.96-7.02 (2H, m), 7.10-7.13 (2H, m), 7.20-7.25 (2H, m), 7.26-7.33 (2H, m), 7.48-7.53 (2H, m), 7.54-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 155(1); Yield: 64.5% (white solid).
1H-NMR (DMSO-d6) δ: 4.89 (2H, s), 7.06-7.12 (2H, m), 7.24-7.34 (4H, m), 7.42 (2H, d, J=8.7 Hz), 7.55 (2H, d, J=8.1 Hz), 7.74 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 126(1) and benzyl chloride; Yield: 60.2% (colorless oil).
1H-NMR (CDCl3) δ: 3.59 (3H, s), 4.92 (2H, s), 6.89-6.94 (2H, m), 7.18-7.23 (2H, m), 7.26-7.30 (3H, m), 7.40-7.45 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 156(1) and 4-(tert-butyl)phenylboronic acid; Yield: 86.5% (yellow oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.56 (3H, s), 4.97 (2H, s), 7.09-7.12 (2H, m), 7.23-7.31 (4H, m), 7.43-7.54 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 156(2); Yield: 65.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.95 (2H, s), 7.22-7.36 (7H, m), 7.45 (2H, d, J=8.4 Hz), 7.53-7.56 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 2-bromoaniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 83% (reddish brown solid).
1H-NMR (CDCl3) δ: 3.77 (2H, brs), 6.78 (1H, dd, J=1.2, 9.0 Hz), 6.84 (1H, dt, J=1.2, 7.5 Hz), 7.10 (1H, dd, J=1.5, 7.5 Hz), 7.15-7.21 (1H, m), 7.27-7.32 (2H, m), 7.45-7.52 (2H, m).
A mixture of the intermediate 157(1) (633 mg, 2.50 mmol), 1-bromo-4-(tert-butyl)benzene (533 mg, 2.50 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (124 mg, 0.2 mmol), bis(dibenzylideneacetone)palladium(0) (72 mg, 0.125 mmol), potassium tert-butoxide (1.68 g, 15.0 mmol) and toluene (10 ml) was stirred at 60° C. for 5 hours under argon atmosphere. After the reaction mixture was cooled to room temperature, a saturated aqueous solution of ammonium chloride was added. The mixture was filtered through Celite, and the filtrate was extracted with ethyl acetate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (857 mg, 89%) as a brown oil.
1H-NMR (CDCl3) δ: 1.31 (9H, s), 5.44 (1H, s), 6.93-7.04 (3H, m), 7.18-7.38 (7H, m), 7.46-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 157(2) and methyl chloroglyoxylate; Yield: 44% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.19 (9H, s), 3.71 (3H, s), 6.53-6.59 (2H, m), 7.00-7.11 (3H, m), 7.13-7.24 (3H, m), 7.29-7.36 (1H, m), 7.39-7.51 (3H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.21 (9H, s), 3.58 (3H, s), 6.58-6.65 (2H, m), 7.00-7.11 (3H, m), 7.13-7.24 (3H, m), 7.29-7.36 (1H, m), 7.39-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 157(3); Yield: 94% (pale brown solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.15 (9H, s), 6.48-6.56 (2H, m), 7.00-7.62 (10H, m), 14.21 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.18 (9H, s), 6.67-6.73 (2H, m), 7.00-7.62 (10H, m), 14.21 (1H, brs).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 3-bromoaniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 83% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.76 (2H, brs), 6.70 (1H, ddd, J=1.8, 2.1, 8.1 Hz), 6.86 (1H, dd, J=1.8, 2.1 Hz), 6.94 (1H, ddd, J=0.9, 1.8, 7.5 Hz), 7.20-7.29 (3H, m), 7.53-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 158(1) and 1-bromo-4-(tert-butyl)benzene; Yield: 90% (brown oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.73 (1H, s), 7.00-7.11 (3H, m), 7.17-7.35 (7H, m), 7.54-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 158(2) and methyl chloroglyoxylate; Yield: 73% (pale brown solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.61 (3H, s), 7.20-7.34 (5H, m), 7.36-7.62 (7H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.62 (3H, s), 7.20-7.34 (5H, m), 7.36-7.62 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 158(3); Yield: 71% (white solid).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 7.17-7.31 (7H, m), 7.35-7.58 (5H, m), 14.17 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-(trifluoromethoxy)benzyl bromide; Yield: 81.5% (colorless oil).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 4.98 (2H, s), 7.10-7.21 (4H, m), 7.24-7.35 (4H, m), 7.48-7.62 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 159(1); Yield: 72.6% (white solid).
1H-NMR (DMSO-d6) δ: 4.98 (2H, s), 7.20-7.67 (10H, m), 7.67-7.81 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-(methylsulfanyl)benzyl chloride; Yield: 34.3% (colorless oil).
1H-NMR (CDCl3) δ: 2.64 (3H, s), 3.58 (3H, s), 4.93 (2H, s), 7.09-7.21 (6H, m), 7.24-7.33 (2H, m), 7.46-7.61 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 160(1); Yield: 97.9% (white solid).
1H-NMR (DMSO-d6) δ: 2.42 (3H, m), 4.90 (2H, s), 7.06-7.50 (8H, m), 7.57 (2H, d, J=8.5 Hz), 7.74 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 4-phenylbenzyl bromide; Yield: 45.6% (white solid).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 5.02 (2H, s), 7.13-7.22 (2H, m), 7.22-7.64 (15H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 161(1); Yield: 87.9% (white solid).
1H-NMR (DMSO-d6) δ: 5.00 (2H, s), 7.26-7.52 (9H, m), 7.52-7.70 (6H, m), 7.75 (2H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-(trifluoromethoxy)benzyl bromide; Yield: 91.8% (colorless oil).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 4.91 (2H, s), 6.87-6.97 (2H, m), 7.08-7.19 (2H, m), 7.19-7.32 (2H, m), 7.40-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 162(1) and 4-(tert-butyl)phenylboronic acid; Yield: 28.5% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.57 (3H, s), 4.97 (2H, s), 7.01-7.20 (4H, m), 7.22-7.35 (2H, m), 7.38-7.60 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 162(2); Yield: 93.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.94 (2H, s), 7.20-7.66 (12H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-(tert-butyl)phenylboronic acid; Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 1.35 (9H, s), 3.56 (3H, s), 4.94 (2H, s), 7.13 (2H, d, J=8.7 Hz), 7.18 (2H, d, J=8.1 Hz), 7.30-7.33 (2H, m), 7.42-7.54 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 163(1); Yield: 62.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 1.30 (9H, s), 4.89 (2H, s), 7.14-7.37 (6H, m), 7.42-7.55 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-butylphenylboronic acid; Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.54-1.62 (4H, m), 2.65 (2H, t, J=8.1 Hz), 3.57 (3H, s), 4.94 (2H, s), 7.11-7.14 (2H, m), 7.17-7.20 (2H, m), 7.23-7.27 (2H, m), 7.29-7.33 (2H, m), 7.42-7.49 (2H, m), 7.50-7.73 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 164(1); Yield: 56.7% (white solid).
1H-NMR (DMSO-d6) δ: 0.90 (3H, t, J=7.2 Hz), 1.24-1.37 (11H, m), 1.52-1.62 (2H, m), 2.59 (2H, d, J=2.7 Hz), 4.90 (2H, s), 7.15-7.35 (8H, m), 7.51-7.57 (4H, m).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 132(1) and 1-bromo-4-(tert-butyl)benzene; Yield: 69% (brown solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 5.59 (1H, brs), 6.91-7.08 (8H, m), 7.12-7.19 (2H, m), 7.27-7.33 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 165(1) and methyl chloroglyoxylate; Yield: 90% (pale brown oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.60 (3H, s), 6.96-7.07 (4H, m), 7.16-7.32 (6H, m), 7.36-7.44 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.66 (3H, s), 6.96-7.07 (4H, m), 7.16-7.32 (6H, m), 7.36-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 165(2); Yield: 83% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 7.05-7.19 (4H, m), 7.19-7.50 (8H, m), 14.15 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 6.93-7.06 (4H, m), 7.19-7.50 (8H, m), 14.15 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromo-3-(trifluoromethyl)aniline and 4-(tert-butyl)benzyl bromide; Yield: 64.3% (yellow oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.28 (2H, s), 4.59 (1H, brs), 6.61 (1H, dd, J=2.7, 9.0 Hz), 6.95 (1H, d, J=2.7 Hz), 7.26-7.28 (2H, m), 7.34-7.43 (3H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 166(1) and methyl chloroglyoxylate; Yield: 76.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.60 (3H, s), 4.91 (2H, s), 7.08-7.13 (3H, m), 7.31-7.34 (3H, m), 7.65 (1H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 166(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 8.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.65 (3H, s), 4.98 (2H, s), 6.81-6.84 (2H, m), 7.05-7.11 (2H, m), 7.16-7.41 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 166(3); Yield: 62.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.93 (2H, s), 7.18-7.24 (2H, m), 7.30-7.35 (3H, m), 7.40-7.44 (4H, m), 7.58-7.61 (1H, m), 7.73 (1H, brs).
Methanesulfonyl chloride (3.069 g, 26.791 mmol) was added to a solution of 4-butylbenzyl alcohol (4.000 g, 24.355 mmol) in dichloromethane (120 mL) at 0° C. under argon atmosphere. Triethylamine (2.711 g, 26.791 mmol) was added dropwise at a slow speed to this mixture, and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure, and the residue was diluted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane) to give the title compound (3.64 g, 82%) as a colorless oil.
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.5 Hz), 1.35 (2H, sext, J=7.5 Hz), 1.52-1.64 (2H, m), 2.60 (2H, t, J=7.5 Hz), 4.57 (2H, s), 7.15-7.18 (2H, m), 7.25-7.30 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 125(3) and the intermediate 167(1); Yield: 83.6% (colorless oil).
1H-NMR (CDCl3) δ: 0.89-0.95 (3H, m), 1.30-1.39 (2H, m), 1.52-1.57 (2H, m), 2.58 (2H, t, J=7.8 Hz), 3.58 (3H, s), 4.94 (2H, s), 7.09-7.16 (6H, m), 7.26-7.30 (2H, m), 7.47-7.51 (2H, m), 7.54-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 167(2); Yield: 84.2% (pale pink solid).
1H-NMR (DMSO-d6) δ: 0.87 (3H, t, J=4.5 Hz), 1.20-1.33 (2H, m), 1.45-1.50 (2H, m), 3.30-3.37 (2H, m), 4.87 (2H, s), 7.06-7.22 (4H, m), 7.34 (2H, d, J=8.1 Hz), 7.41 (2H, d, J=8.1 Hz), 7.54 (2H, d, J=8.4 Hz), 7.71-7.76 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 2-bromo-5-(trifluoromethyl)aniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 4.02 (2H, brs), 6.78 (1H, d, J=8.7 Hz), 7.29-7.36 (3H, m), 7.37-7.44 (1H, m), 7.44-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 168(1) and methyl chloroglyoxylate; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 3.92 (3H, s), 7.38-7.47 (5H, m), 7.50-7.56 (1H, m), 8.76-8.79 (1H, m), 9.02 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 168(2) and 4-(tert-butyl)benzyl bromide; Yield: 73% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.25 (9H, s), 3.43 (1H, d, J=14.4 Hz), 3.66 (3H, s), 5.20 (1H, d, J=14.4 Hz), 6.82-6.98 (3H, m), 7.16-7.58 (2H, m), 7.32-7.40 (2H, m), 7.51 (1H, d, J=7.8 Hz), 7.60-7.69 (3H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.27 (9H, s), 3.43 (1H, d, J=14.4 Hz), 3.90 (3H, s), 5.20 (1H, d, J=14.4 Hz), 6.82-7.69 (11H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 168(3); Yield: 93% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.21 (9H, s), 3.42 (1H, d, J=14.4 Hz), 5.03 (1H, d, J=14.4 Hz), 6.83-6.94 (2H, m), 7.00-7.09 (1H, m), 7.15-7.44 (3H, m), 7.60-7.87 (5H, m), 14.67 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.01-4.18 (1H, m), 4.57-4.70 (1H, m), 6.84-7.87 (11H, m), 14.67 (1H, brs).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 2-bromo-4-(trifluoromethyl)aniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 98% (pale brown oil).
1H-NMR (CDCl3) δ: 4.02 (2H, brs), 6.78 (1H, d, J=8.7 Hz), 7.29-7.36 (3H, m), 7.37-7.44 (1H, m), 7.44-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 169(1) and methyl chloroglyoxylate; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 3.92 (3H, s), 7.38-7.50 (4H, m), 7.54-7.58 (1H, m), 7.67-7.75 (1H, m), 8.63 (1H, d, J=8.4 Hz), 9.08 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 169(2) and 4-(tert-butyl)benzyl bromide; Yield: 84% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.26 (9H, s), 3.50 (1H, d, J=14.4 Hz), 3.67 (3H, s), 5.14 (1H, d, J=14.4 Hz), 6.85-7.00 (3H, m), 7.15-7.51 (5H, m), 7.55-7.67 (3H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.50 (1H, d, J=14.4 Hz), 3.88 (3H, s), 5.14 (1H, d, J=14.4 Hz), 6.85-7.67 (11H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 169(3); Yield: 94% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 3.42 (1H, d, J=14.7 Hz), 4.91 (1H, d, J=14.7 Hz), 6.89-6.98 (2H, m), 7.17-7.42 (3H, m), 7.51-7.59 (2H, m), 7.70-7.86 (4H, m), 14.48 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.12-4.30 (1H, m), 4.47-4.70 (1H, m), 6.89-7.86 (11H, m), 14.48 (1H, brs).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 1,3-dinitrobenzene and 4-(trifluoromethoxy)phenol; Yield: 74% (pale yellow oil).
1H-NMR (CDCl3) δ: 7.05-7.11 (2H, m), 7.23-7.30 (2H, m), 7.33 (1H, ddd, J=0.9, 2.4, 8.4 Hz), 7.52 (1H, t, J=8.4 Hz), 7.82 (1H, t, J=2.4 Hz), 7.98 (1H, ddd, J=0.9, 2.4, 8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 170(1); Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 3.73 (2H, brs), 6.33 (1H, t, J=2.4 Hz), 6.39 (1H, ddd, J=0.9, 2.4, 8.1 Hz), 6.45 (1H, ddd, J=0.9, 2.4, 8.1 Hz), 6.98-7.04 (2H, m), 7.11 (1H, t, J=8.1 Hz), 7.13-7.20 (2H, m).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 170(2) and 1-bromo-4-(tert-butyl)benzene; Yield: 69% (orange oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 5.69 (1H, brs), 6.48 (1H, ddd, J=0.9, 2.1, 8.4 Hz), 6.69 (1H, t, J=2.4 Hz), 6.76 (1H, ddd, J=0.9, 2.4, 8.4 Hz), 6.98-7.06 (4H, m), 7.13-7.22 (3H, m), 7.27-7.32 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 170(3) and methyl chloroglyoxylate; Yield: 84% (pale yellow solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.31 (9H, m), 3.58 (3H, s), 6.87-7.25 (9H, m), 7.29-7.44 (3H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.31 (9H, m), 3.66 (3H, s), 6.87-7.25 (9H, m), 7.29-7.44 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 170(4); Yield: 94% (white solid).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 6.90-7.35 (6H, m), 7.36-7.50 (6H, m), 14.24 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromoaniline and 2,6-dichlorobenzyl chloride; Yield: 41.0% (white solid).
1H-NMR (CDCl3) δ: 4.02 (1H, brs), 4.55 (2H, s), 6.62-6.67 (2H, m), 7.15-7.21 (1H, m), 7.24-7.29 (2H, m), 7.33 (2H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 171(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 36.3% (white solid).
1H-NMR (CDCl3) δ: 4.13 (1H, brs), 4.64 (2H, s), 6.82-6.86 (2H, m), 7.16-7.25 (3H, m), 7.34 (2H, d, J=7.8 Hz), 7.40-7.45 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 171(2) and methyl chloroglyoxylate; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 3.56 (3H, s), 5.38 (2H, s), 7.06-7.12 (1H, m), 7.15-7.22 (4H, m), 7.25-7.27 (2H, m), 7.38-7.42 (2H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 171(3); Yield: 67.8% (white solid).
1H-NMR (DMSO-d6) δ: 5.24 (2H, s), 7.23-7.27 (3H, m), 7.35-7.42 (4H, m), 7.57 (2H, d, J=8.1 Hz), 7.72 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 170(2) and methyl chloroglyoxylate; Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 3.97 (3H, s), 6.80-6.88 (1H, m), 7.00-7.07 (2H, m), 7.17-7.24 (2H, m), 7.33-7.42 (3H, m), 8.84 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 172(1) and 4-(tert-butyl)benzyl bromide; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.60 (3H, s), 4.90 (2H, s), 6.73 (1H, t, J=2.4 Hz), 6.84-6.98 (4H, m), 7.11-7.23 (4H, m), 7.25-7.32 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 172(2); Yield: 90.8% (colorless oil).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.88 (2H, s), 6.88 (1H, brs), 6.95-7.12 (6H, m), 7.30 (2H, d, J=7.8 Hz), 7.35-7.40 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromo-2,6-dichloroaniline and 4-(tert-butyl)benzyl bromide; Yield: 20.2% (red oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.23 (1H, brs), 4.44 (2H, s), 7.29-7.38 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 173(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 42.3% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.34 (1H, brs), 4.52 (2H, s), 7.25-7.29 (2H, m), 7.34-7.41 (4H, m), 7.45 (2H, s), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 173(2) and methyl chloroglyoxylate; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (9H, s), 3.68 (3H, s), 4.93 (2H, s), 7.16-7.20 (2H, m), 7.22-7.26 (2H, m), 7.29-7.33 (2H, m), 7.49 (2H, s), 7.55-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 173(3); Yield: 31.3% (pale orange solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.80 (2H, s), 7.17-7.29 (4H, m), 7.44-7.47 (2H, m), 7.76-7.77 (2H, m), 7.86 (2H, d, J=8.4 Hz).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.73 (2H, s), 7.17-7.29 (4H, m), 7.44-7.47 (2H, m), 7.76-7.77 (2H, m), 7.86 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 4-fluoro-1-nitro-2-(trifluoromethyl)benzene and 4-(trifluoromethoxy)phenol; Yield: 88% (pale yellow oil).
1H-NMR (CDCl3) δ: 7.10-7.19 (3H, m), 7.29-7.36 (2H, m), 7.41 (1H, d, J=3.0 Hz), 7.98 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 174(1); Yield: 99% (gray oil).
1H-NMR (CDCl3) δ: 4.10 (2H, brs), 6.76 (1H, d, J=9.0 Hz), 6.88-6.94 (2H, m), 7.03 (1H, dd, J=2.7, 8.7 Hz), 7.12-7.19 (3H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 174(2) and methyl chloroglyoxylate; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 4.01 (3H, s), 7.01-7.07 (2H, m), 7.18-7.27 (3H, m), 7.32 (1H, d, J=2.7 Hz), 8.26 (1H, d, J=9.0 Hz), 9.22 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 174(3) and 4-(tert-butyl)benzyl bromide; Yield: 94% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.62 (3H, s), 3.65 (1H, d, J=14.4 Hz), 5.75 (1H, d, J=14.4 Hz), 6.78 (1H, d, J=9.0 Hz), 6.92 (1H, dd, J=3.0, 9.0 Hz), 7.02-7.08 (2H, m), 7.13-7.20 (2H, m), 7.21-7.37 (5H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.94 (3H, s), 4.36 (1H, d, J=14.4 Hz), 5.11 (1H, d, J=14.4 Hz), 6.72 (1H, d, J=9.0 Hz), 6.89-6.96 (1H, m), 7.02-7.08 (2H, m), 7.13-7.20 (2H, m), 7.21-7.37 (5H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 174(4); Yield: 91% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.24 (9H, s), 4.05 (1H, d, J=14.4 Hz), 5.39 (1H, d, J=14.4 Hz), 6.99 (1H, d, J=8.4 Hz), 7.12-7.23 (5H, m), 7.30-7.36 (2H, m), 7.40-7.48 (3H, m), 14.00 (1H, brs).
Minor isomer: 1H-NMR (CDCl3) δ: 1.23 (9H, s), 4.42 (1H, d, J=15.6 Hz), 5.03 (1H, d, J=15.6 Hz), 6.90 (1H, d, J=8.4 Hz), 7.12-7.23 (5H, m), 7.30-7.36 (2H, m), 7.40-7.48 (3H, m), 14.00 (1H, brs).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 1,3-dinitro-5-(trifluoromethyl)benzene and 4-(trifluoromethoxy)phenol; Yield: 75% (orange oil).
1H-NMR (CDCl3) δ: 7.09-7.16 (2H, m), 7.30-7.36 (2H, m), 7.57 (1H, brs), 7.95 (1H, t, J=2.1 Hz), 8.22 (1H, brs).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 175(1); Yield: 99% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.90 (2H, brs), 6.42 (1H, t, J=2.4 Hz), 6.61 (1H, brs), 6.65 (1H, brs), 7.00-7.05 (2H, m), 7.18-7.24 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 175(2) and methyl chloroglyoxylate; Yield: 7% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.98 (3H, s), 7.04-7.10 (3H, m), 7.22-7.29 (2H, m), 7.57-7.63 (2H, m), 8.96 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 175(3) and 4-(tert-butyl)benzyl bromide; Yield: 85% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.64 (3H, s), 4.90 (2H, s), 6.86 (1H, t, J=2.1 Hz), 6.92-7.00 (2H, m), 7.02 (1H, brs), 7.07-7.14 (2H, m), 7.12 (1H, brs), 7.20-7.26 (2H, m), 7.27-7.33 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 175(4); Yield: 71% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.92 (2H, s), 7.04-7.17 (5H, m), 7.26-7.47 (6H, m), 14.45 (1H, brs).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 3-bromo-4-methylaniline and methyl chloroglyoxylate; Yield: 92.5% (white solid).
1H-NMR (CDCl3) δ: 2.38 (3H, s), 3.98 (3H, s), 7.23 (1H, d, J=8.2 Hz), 7.49 (1H, dd, J=2.2, 8.2 Hz), 7.87 (1H, d, J=2.2 Hz), 8.79 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 176(1) and 4-(tert-butyl)benzyl bromide; Yield: 83.3% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.37 (3H, s), 3.61 (3H, s), 4.87 (2H, s), 6.90 (1H, dd, J=2.2, 8.2 Hz), 7.07-7.21 (3H, m), 7.27 (1H, d, J=2.2 Hz), 7.28-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 176(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 73.9% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.23 (3H, s), 3.58 (3H, s), 4.91 (2H, s), 6.79 (1H, d, J=2.2 Hz), 7.01 (1H, dd, J=2.2, 8.0 Hz), 7.08-7.27 (7H, m), 7.27-7.37 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 176(3); Yield: 56.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 2.17 (3H, s), 4.84 (2H, s), 6.90-7.22 (4H, m), 7.22-7.33 (3H, m), 7.33-7.50 (4H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 3-bromo-2-methylaniline and 4-(tert-butyl)benzyl bromide; Yield: 45.5% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.55 (1H, brs), 2.27 (3H, s), 4.32 (2H, s), 6.61-6.64 (1H, m), 6.94 (1H, t, J=7.8 Hz), 6.98-7.00 (1H, m), 7.28-7.31 (2H, m), 7.37-7.40 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 177(1) and methyl chloroglyoxylate; Yield: 95.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.24 (3H, s), 3.52 (3H, s), 4.24 (1H, d, J=14.1 Hz), 5.30 (1H, d, J=14.1 Hz), 6.73-6.76 (1H, m), 6.94 (1H, t, J=8.1 Hz), 7.10-7.12 (2H, m), 7.27-7.30 (2H, m), 7.52-7.55 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 177(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 81.0% (brown oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.02 (3H, s), 3.53 (3H, s), 4.34 (1H, d, J=13.8 Hz), 5.30 (1H, d, J=13.8 Hz), 6.85 (1H, dd, J=1.8, 8.1 Hz), 7.10-7.33 (10H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.05 (3H, s), 3.52 (3H, s), 4.60 (1H, d, J=13.8 Hz), 4.84 (1H, d, J=13.8 Hz), 6.74 (1H, dd, J=1.8, 8.1 Hz), 6.81-6.84 (2H, m), 7.08-7.23 (7H, m), 7.54 (1H, dd, J=1.8, 8.1 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 177(3); Yield: 23.8% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.07 (3H, s), 4.11 (1H, d, J=14.7 Hz), 5.17 (1H, d, J=14.7 Hz), 6.89-6.93 (1H, m), 7.08-7.18 (3H, m), 7.25-7.43 (7H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 1.73 (3H, s), 4.64 (1H, d, J=14.7 Hz), 4.90 (1H, d, J=14.7 Hz), 6.89-6.93 (1H, m), 7.08-7.18 (3H, m), 7.25-7.43 (7H, m).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: 1,3-dibromo-5-methylbenzene and 4-(tert-butyl)benzylamine; Yield: 84.2% (yellow oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.23 (3H, s), 3.95 (1H, brs), 4.24 (2H, s), 6.36 (1H, s), 6.60 (1H, s), 6.68 (1H, s), 7.25-7.29 (2H, m), 7.37-7.39 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 178(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 90.9% (brown oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.33 (3H, s), 4.03 (1H, brs), 4.33 (2H, s), 6.49 (1H, s), 6.62 (1H, s), 6.72 (1H, s), 7.22-7.25 (2H, m), 7.32 (2H, d, J=8.4 Hz), 7.39 (2H, d, J=8.4 Hz), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 178(2) and methyl chloroglyoxylate; Yield: 89.3% (brown oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.37 (3H, s), 3.56 (3H, s), 4.94 (2H, s), 6.90-6.95 (2H, m), 7.16-7.19 (2H, m), 7.21-7.26 (2H, m), 7.30 (1H, brs), 7.32-7.34 (2H, m), 7.38-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 178(3); Yield: 19.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.29 (3H, s), 4.90 (2H, s), 7.11-7.48 (3H, m), 7.26-7.43 (6H, m), 7.63-7.67 (2H, m).
A mixture of 4-(tert-butyl)benzyl bromide (6.252 g, 27.522 mmol), 4-bromo-2-nitrophenol (5.0 g, 22.934 mmol), potassium carbonate (12.679 g, 91.736 mmol) and dimethylformamide (40 ml) was stirred at 50° C. for 3 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (8.1 g, 97.0%) as a white solid.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.19 (2H, s), 7.02 (1H, d, J=8.7 Hz), 7.34-7.43 (4H, m), 7.58 (1H, dd, J=2.7, 8.7 Hz), 7.97 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 179(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 74.6% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.26 (2H, s), 7.22 (1H, d, J=8.7 Hz), 7.28-7.58 (8H, m), 7.68 (1H, dd, J=2.4, 8.7 Hz), 8.05 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 179(2); Yield: 83.5% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.93 (2H, brs), 5.09 (2H, s), 6.87-6.97 (3H, m), 7.22-7.57 (8H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 179(3) and benzyl bromide; Yield: 93% (yellow oil).
1H-NMR (CDCl3) δ: 1.41 (9H, s), 4.65-4.72 (2H, m), 4.96 (1H, brs), 5.25 (2H, s), 7.02-7.06 (1H, m), 7.15-7.25 (4H, m), 7.26-7.40 (2H, m), 7.56-7.61 (4H, m), 7.64-7.67 (4H, m), 7.89-7.91 (1H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 179(4) and methyl chloroglyoxylate; Yield: 31% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.53 (3H, s), 4.44 (1H, d, J=14.4 Hz), 5.10 (2H, s), 5.43 (1H, d, J=14.4 Hz), 7.01-7.05 (2H, m), 7.19-7.26 (7H, m), 7.30-7.36 (4H, m), 7.41-7.45 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 179(5); Yield: 67% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.19-4.25 (1H, m), 5.21 (2H, s), 5.38-5.44 (1H, m), 7.13-7.26 (6H, m), 7.35-7.53 (10H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.90-5.21 (2H, m), 5.15 (2H, s), 7.13-7.26 (6H, m), 7.35-7.53 (10H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 2,6-dichloro-4-bromoaniline and methyl chloroglyoxylate; Yield: 93.0% (pink solid).
1H-NMR (CDCl3) δ: 4.01 (3H, s), 7.58 (2H, s), 8.51 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 180(1) and benzyl bromide; Yield: 99.9% (red oil).
1H-NMR (CDCl3) δ: 3.69 (3H, s), 4.92 (2H, s), 7.21-7.29 (5H, m), 7.47 (2H, s).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 180(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 91.6% (red oil).
1H-NMR (CDCl3) δ: 3.69 (3H, s), 4.98 (2H, s), 7.22-7.32 (7H, m), 7.49 (2H, s), 7.54-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 180(3); Yield: 94.5% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 4.76 (2H, s), 7.17-7.22 (4H, m), 7.34-7.37 (1H, m), 7.44 (2H, d, J=8.4 Hz), 7.70-7.75 (2H, m), 7.84-7.88 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 4.72 (2H, s), 7.17-7.22 (4H, m), 7.34-7.37 (1H, m), 7.44 (2H, d, J=8.4 Hz), 7.70-7.75 (2H, m), 7.84-7.88 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-(chloromethyl)phenyl acetate; Yield: 43.9% (colorless oil).
1H-NMR (CDCl3) δ: 2.29 (3H, s), 3.59 (3H, s), 4.90 (2H, s), 6.89-6.98 (2H, m), 6.98-7.08 (2H, m), 7.18-7.26 (2H, m), 7.40-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 181(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 26.3% (pale brown oil).
1H-NMR (CDCl3) δ: 2.59 (3H, s), 3.59 (3H, s), 4.96 (2H, s), 6.95-7.10 (2H, m), 7.10-7.20 (2H, m), 7.20-7.38 (4H, m), 7.42-7.67 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 181(2); Yield: 90.6% (white solid).
1H-NMR (DMSO-d6) δ: 4.79 (2H, s), 6.54-6.74 (2H, m), 6.90-7.36 (4H, m), 7.36-7.48 (2H, m), 7.48-7.65 (2H, m), 7.68-7.84 (2H, m), 9.31 (1H, s).
4-Bromo-2-nitrophenol (1.00 g, 4.59 mmol) was added by small portions to a suspension of sodium hydride (400 mg, 9.17 mmol) in dimethylformamide (12 ml) at room temperature under argon atmosphere, and the mixture was stirred at room temperature for 30 minutes. A solution of methyl iodide (1.30 g, 9.174 mmol) in dimethylformamide (4 ml) was added to this mixture, and the mixture was stirred at room temperature for 6 hours. The reaction mixture was diluted with water and extracted with diisopropyl ether. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (658 mg, 61.8%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 3.96 (3H, s), 6.99 (1H, d, J=9.1 Hz), 7.65 (1H, dd, J=2.5, 9.1 Hz), 7.98 (1H, d, J=2.5 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 182(1); Yield: 52.1% (brown solid).
1H-NMR (DMSO-d6) δ: 3.74 (3H, s), 5.01 (2H, s), 6.61 (1H, dd, J=2.5, 8.5 Hz), 6.71 (1H, d, J=8.5 Hz), 6.75 (1H, d, J=2.5 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 182(2) and methyl chloroglyoxylate; Yield: 91.0% (pale brown solid).
1H-NMR (CDCl3) δ: 3.91 (3H, s), 3.98 (3H, s), 6.79 (1H, d, J=8.5 Hz), 7.25 (1H, d, J=2.5, 8.5 Hz), 8.58 (1H, d, J=2.5 Hz), 9.44 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 182(3) and 4-(tert-butyl)benzyl bromide; Yield: 77.8% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.60 (3H, s), 3.73 (3H, s), 4.46 (1H, d, J=14.1 Hz), 5.19 (1H, d, J=14.1 Hz), 6.76 (1H, d, J=8.8 Hz), 7.01 (1H, d, J=2.5 Hz), 7.08-7.17 (2H, m), 7.25-7.33 (2H, m), 7.37 (1H, dd, J=2.5, 8.8 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 182(4) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 36.5% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.54 (3H, s), 3.85 (3H, s), 4.30 (1H, d, J=14.1 Hz), 5.45 (1H, d, J=14.1 Hz), 6.91 (1H, d, J=2.5 Hz), 6.98 (1H, d, J=8.5 Hz), 7.08-7.22 (4H, m), 7.22-7.40 (4H, m), 7.46 (1H, dd, J=2.5, 8.5 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 182(5); Yield: 74.3% (pale orange solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 3.83 (3H, s), 4.14-4.50 (1H, m), 5.06-5.42 (1H, m), 7.08-7.15 (2H, m), 7.15-7.22 (2H, m), 7.26-7.33 (2H, m), 7.33-7.42 (2H, m), 7.46-7.56 (2H, m), 7.59 (1H, dd, J=2.5, 8.5 Hz).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.21 (9H, s), 3.76 (3H, s), 4.56-4.88 (2H, m), 6.90-7.64 (11H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-(trifluoromethoxy)benzyl chloride; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 4.91 (2H, s), 6.90-6.95 (2H, m), 7.13-7.16 (2H, m), 7.22-7.27 (2H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 183(1) and phenylboronic acid; Yield: 80.7% (yellow oil).
1H-NMR (CDCl3) δ: 3.59 (3H, s), 4.97 (2H, s), 7.10-7.17 (4H, m), 7.28-7.31 (2H, m), 7.37-7.47 (3H, m), 7.54-7.58 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 183(2); Yield: 66.3% (white solid).
1H-NMR (DMSO-d6) δ: 4.93 (2H, s), 7.30-7.35 (6H, m), 7.41-7.46 (3H, m), 7.53-7.56 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 4-bromo-3-methylaniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 92% (brown oil).
1H-NMR (CDCl3) δ: 2.20 (3H, s), 3.68 (2H, brs), 6.56-6.63 (2H, m), 7.01 (1H, d, J=8.1 Hz), 7.18-7.32 (4H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 184(1) and methyl chloroglyoxylate; Yield: 95% (pale orange solid).
1H-NMR (CDCl3) δ: 2.28 (3H, s), 3.99 (3H, s), 7.20-7.36 (5H, m), 7.52-7.57 (2H, m), 8.86 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 184(2) and 4-(tert-butyl)benzyl bromide; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.19 (3H, s), 3.62 (3H, s), 4.94 (2H, s), 6.95 (1H, dd, J=1.8, 8.1 Hz), 7.01 (1H, d, J=1.8 Hz), 7.13 (1H, d, J=8.1 Hz), 7.17-7.36 (8H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 184(3); Yield: 94% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 2.12 (3H, s), 4.92 (2H, s), 7.06-7.27 (5H, m), 7.29-7.48 (6H, m), 14.08 (1H, brs).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 3-bromo-4-chloro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99.9% (brown oil).
1H-NMR (CDCl3) δ: 7.33-7.36 (2H, m), 7.48-7.52 (2H, m), 7.67 (1H, d, J=8.7 Hz), 8.18 (1H, dd, J=2.7, 8.7 Hz), 8.23 (1H, d, J=2.7 Hz).
1-Propanol (284 mg, 4.72 mmol) was added dropwise at a slow speed to a suspension of sodium hydride (206 mg, 4.72 mmol) in dimethylformamide (4 ml) at 0° C. under argon atmosphere, and the mixture was stirred at room temperature for 30 minutes. A solution of the intermediate 185(1) (1.00 g, 3.15 mmol) in dimethylformamide (2 ml) was added dropwise at a slow speed to this mixture at 0° C., and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (586 mg, 54.5%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.5 Hz), 1.75-1.85 (2H, m), 4.07 (2H, t, J=6.6 Hz), 7.01-7.04 (1H, m), 7.26-7.30 (2H, m), 7.55-7.60 (2H, m), 8.22-8.26 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 185(2); Yield: 97.7% (black oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.2 Hz), 1.61-1.70 (2H, m), 3.49 (2H, brs), 3.80 (2H, t, J=6.6 Hz), 6.64-6.69 (2H, m), 6.83 (1H, d, J=8.1 Hz), 7.20-7.23 (2H, m), 7.53-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 185(3) and 4-(tert-butyl)benzyl bromide; Yield: 12.0% (yellow oil).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.5 Hz), 1.32 (9H, s), 1.60-1.71 (2H, m), 3.79 (2H, t, J=6.3 Hz), 4.09-4.16 (1H, m), 4.27 (2H, s), 6.60-6.63 (2H, m), 6.86 (1H, d, J=8.7 Hz), 7.20-7.23 (2H, m), 7.30-7.33 (2H, m), 7.37-7.40 (2H, m), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 185(4) and methyl chloroglyoxylate; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.30 (9H, s), 1.70-1.79 (2H, m), 3.57 (3H, s), 3.89-3.94 (2H, m), 4.88 (2H, s), 6.84-6.87 (2H, m), 7.04 (1H, dd, J=2.4, 8.4 Hz), 7.15-7.19 (4H, m), 7.31-7.39 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 185(5); Yield: 69.8% (white solid).
1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=7.2 Hz), 1.24 (9H, s), 1.61-1.68 (2H, m), 3.90 (2H, t, J=6.0 Hz), 4.81 (2H, s), 6.96-7.13 (4H, m), 7.19-7.22 (1H, m), 7.28-7.37 (4H, m), 7.44-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 185(1); Yield: 94.5% (yellow oil).
1H-NMR (CDCl3) δ: 3.89 (2H, brs), 6.61-6.65 (2H, m), 7.21-7.27 (3H, m), 7.43-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 186(1) and 4-(tert-butyl)benzyl bromide; Yield: 24.5% (brown oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.07 (1H, brs), 4.28 (2H, s), 6.55-6.58 (2H, m), 7.22-7.30 (5H, m), 7.37-7.40 (2H, m), 7.42-7.45 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 186(2) and methyl chloroglyoxylate; Yield: 76.2% (yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.61 (3H, s), 4.91 (2H, s), 6.89 (1H, d, J=2.7 Hz), 7.05 (1H, dd, J=2.7, 8.4 Hz), 7.13-7.16 (2H, m), 7.21-7.34 (6H, m), 7.43 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 186(3); Yield: 76.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.91 (2H, s), 7.10-7.18 (2H, m), 7.22-7.33 (4H, m), 7.43-7.54 (5H, m).
A mixture of 2-methyl-5-nitrophenol (765 mg, 5.00 mmol), 4-(trifluoromethoxy)phenylboronic acid (1.24 g, 6.00 mmol), copper(II) acetate (999 mg, 5.50 mmol), triethylamine (3.48 ml, 25.0 mmol), molecular sieves 4A and dichloromethane (20.0 ml) was stirred at room temperature overnight under argon atmosphere. The reaction mixture was filtered through Celite. The residue obtained by evaporation of the solvent of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=20:1) to give the title compound (323 mg, 20.6%) as a colorless oil.
1H-NMR (CDCl3) δ: 2.39 (3H, s), 6.96-7.03 (2H, m), 7.22-7.26 (2H, m), 7.42 (1H, d, J=8.4 Hz), 7.68 (1H, d, J=2.1 Hz), 7.94 (1H, dd, J=2.1, 8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 187(1); Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 2.09 (3H, s), 3.58 (2H, brs), 6.26 (1H, d, J=2.1 Hz), 6.44 (1H, dd, J=2.1, 8.1 Hz), 6.86-6.92 (2H, m), 7.02 (1H, d, J=8.1 Hz), 7.10-7.13 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 187(2) and methyl chloroglyoxylate; Yield: 98.7% (white solid).
1H-NMR (CDCl3) δ: 2.22 (3H, s), 3.95 (3H, s), 6.89-6.96 (2H, m), 7.14-7.20 (2H, m), 7.23-7.28 (2H, m), 7.34 (1H, dd, J=2.1, 8.4 Hz), 8.78 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 187(3) and 4-(tert-butyl)benzyl bromide; Yield: 37.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (9H, s), 2.19 (3H, s), 3.58 (3H, s), 4.86 (2H, s), 6.60 (1H, d, J=2.1 Hz), 6.75-6.80 (2H, m), 6.84 (1H, dd, J=2.1, 8.1 Hz), 7.09-7.16 (4H, m), 7.20 (1H, d, J=8.1 Hz), 7.24-7.29 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 187(4); Yield: 27.2% (white solid).
1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 2.12 (3H, s), 4.84 (2H, s), 6.69 (1H, d, J=2.1 Hz), 6.85-6.91 (2H, m), 7.03 (1H, dd, J=2.1, 8.1 Hz), 7.08 (2H, d, J=8.4 Hz), 7.30 (2H, d, J=8.4 Hz), 7.31-7.37 (3H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 5-bromo-2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99.9% (brown oil).
1H-NMR (CDCl3) δ: 7.33-7.43 (3H, m), 7.57-7.62 (2H, m), 7.79-7.84 (1H, m), 8.23 (1H, dd, J=2.4, 6.9 Hz).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-propanol; Yield: 64.4% (yellow oil).
1H-NMR (CDCl3) δ: 1.09 (3H, t, J=7.2 Hz), 1.83-1.96 (2H, m), 4.12 (2H, t, J=6.3 Hz), 7.15 (1H, d, J=8.7 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.69 (1H, dd, J=2.4, 8.7 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 188(2); Yield: 95.5% (white solid).
1H-NMR (CDCl3) δ: 1.07 (3H, t, J=7.5 Hz), 1.81-1.89 (2H, m), 3.90 (2H, brs), 4.00 (2H, t, J=6.0 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.22-7.24 (2H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 188(3) and methyl chloroglyoxylate; Yield: 97.0% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.12 (3H, t, J=7.5 Hz), 1.89-1.96 (2H, m), 3.99 (3H, s), 4.09 (2H, t, J=6.6 Hz), 6.98 (1H, d, J=8.4 Hz), 7.25-7.33 (3H, m), 7.57-7.62 (2H, m), 8.68 (1H, d, J=2.1 Hz), 9.62 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 188(4) and 4-(tert-butyl)benzyl bromide; Yield: 88.7% (brown oil).
1H-NMR (CDCl3) δ: 1.06 (3H, t, J=7.5 Hz), 1.28 (9H, s), 1.76-1.83 (2H, m), 3.53 (3H, s), 3.89-3.99 (2H, m), 4.39 (1H, d, J=14.4 Hz), 5.38 (1H, d, J=14.4 Hz), 6.94-6.97 (2H, m), 7.13-7.20 (4H, m), 7.26-7.33 (4H, m), 7.41-7.45 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 188(5); Yield: 55.6% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.99 (3H, t, J=7.2 Hz), 1.21 (9H, s), 1.69-1.76 (2H, m), 3.90-3.99 (2H, m), 4.40-4.44 (1H, m), 5.18-5.23 (1H, m), 7.09-7.14 (2H, m), 7.25-7.38 (6H, m), 7.46-7.55 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.97-1.04 (3H, m), 1.27 (9H, s), 1.69-1.76 (2H, m), 3.90-3.99 (2H, m), 4.75-4.82 (1H, m), 5.18-5.23 (1H, m), 7.00-7.14 (2H, m), 7.25-7.38 (6H, m), 7.46-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-butanol; Yield: 30.9% (yellow solid).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.5 Hz), 1.50-1.58 (2H, m), 1.80-1.88 (2H, m), 4.15 (2H, t, J=6.3 Hz), 7.15 (1H, d, J=8.7 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.69 (1H, dd, J=2.4, 6.3 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 189(1); Yield: 98.1% (white solid).
1H-NMR (CDCl3) δ: 1.00 (3H, t, J=7.5 Hz), 1.47-1.59 (2H, m), 1.78-1.87 (2H, m), 3.90 (2H, brs), 4.04 (2H, t, J=6.3 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.21-7.25 (2H, m), 7.50-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 189(2) and methyl chloroglyoxylate; Yield: 94.0% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=7.2 Hz), 1.53-1.61 (2H, m), 1.84-1.91 (2H, m), 3.99 (3H, s), 4.13 (2H, t, J=6.6 Hz), 6.98 (1H, d, J=8.7 Hz), 7.25-7.33 (3H, m), 7.57-7.62 (2H, m), 8.68 (1H, d, J=2.1 Hz), 9.61 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 189(3) and 4-(tert-butyl)benzyl bromide; Yield: 86.6% (colorless oil).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.5 Hz), 1.28 (9H, s), 1.45-1.55 (2H, m), 1.73-1.79 (2H, m), 3.53 (3H, s), 3.95-3.99 (2H, m), 4.38 (1H, d, J=14.4 Hz), 5.38 (1H, d, J=14.4 Hz), 6.94-6.97 (2H, m), 7.13-7.20 (4H, m), 7.26-7.33 (4H, m), 7.41-7.45 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 189(4); Yield: 80.4% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.95 (3H, t, J=7.2 Hz), 1.24 (9H, s), 1.40-1.48 (2H, m), 1.69-1.74 (2H, m), 3.90-3.99 (2H, m), 4.40-4.44 (1H, m), 5.18-5.23 (1H, m), 7.09-7.14 (2H, m), 7.25-7.38 (6H, m), 7.46-7.55 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.95 (3H, t, J=7.2 Hz), 1.26 (9H, s), 1.40-1.48 (2H, m), 1.69-1.74 (2H, m), 3.90-3.99 (2H, m), 4.78-4.84 (1H, m), 5.18-5.23 (1H, m), 7.00-7.14 (2H, m), 7.25-7.38 (6H, m), 7.46-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 5-chloro-2,4-dimethoxyaniline and methyl chloroglyoxylate; Yield: 52.4% (pale purple solid).
1H-NMR (CDCl3) δ: 3.91 (3H, s), 3.94 (3H, s), 3.97 (3H, s), 6.54 (1H, s), 8.46 (1H, s), 9.26 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 190(1) and 4-(tert-butyl)benzyl bromide; Yield: 87.8% (pale purple oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.59 (3H, s), 3.76 (3H, s), 3.90 (3H, s), 4.36 (1H, d, J=14.1 Hz), 5.19 (1H, d, J=14.1 Hz), 6.45 (1H, s), 6.86 (1H, s), 7.11 (2H, d, J=8.1 Hz), 7.28 (2H, d, J=8.1 Hz).
A mixture of the intermediate 190(2) (800 mg, 1.91 mmol), 4-(trifluoromethoxy)phenylboronic acid (549 mg, 2.67 mmol), palladium(II) acetate (21 mg, 0.095 mmol), potassium fluoride (332 mg, 5.72 mmol), 2-(di-tert-butylphosphino)biphenyl (57 mg, 0.191 mmol) and tetrahydrofuran (3.0 ml) was refluxed for 5 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (140 mg, 14%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 3.84 (3H, s), 3.87 (3H, s), 4.20 (1H, d, J=13.8 Hz), 5.43 (1H, d, J=13.8 Hz), 6.51 (1H, s), 6.62 (1H, s), 7.09-7.15 (4H, m), 7.19-7.24 (2H, m), 7.27-7.32 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 190(3); Yield: 69.5% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 3.83 (3H, s), 3.88 (3H, s), 4.18 (1H, d, J=14.7 Hz), 5.25 (1H, d, J=14.7 Hz), 6.66 (1H, s), 6.82 (1H, s), 7.11 (2H, d, J=8.4 Hz), 7.28-7.35 (6H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 3.80 (3H, s), 3.82 (3H, s), 4.28-4.38 (1H, m), 5.05-5.11 (1H, m), 6.61-7.34 (10H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 4-chloro-2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenol; Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 6.83-6.87 (2H, m), 6.99 (1H, d, J=2.1 Hz), 7.05-7.12 (2H, m), 7.21 (1H, dd, J=2.1, 9.0 Hz), 7.96 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 191(1); Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 3.81 (2H, brs), 6.80-6.84 (2H, m), 6.94-7.01 (3H, m), 7.17-7.20 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 191(2) and methyl chloroglyoxylate; Yield: 64.1% (yellow oil).
1H-NMR (CDCl3) δ: 3.96 (3H, s), 6.83 (1H, d, J=2.1 Hz), 7.05-7.13 (2H, m), 7.15 (1H, dd, J=2.1, 9.0 Hz), 7.22-7.26 (2H, m), 8.45 (1H, d, J=9.0 Hz), 9.40 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 191(3) and 4-(tert-butyl)benzyl bromide; Yield: 99.9% (brown oil).
1H-NMR (CDCl3) δ: 1.27 (9H, s), 3.66 (3H, s), 4.72 (1H, d, J=14.1 Hz), 5.08 (1H, d, J=14.1 Hz), 6.70 (1H, d, J=2.1 Hz), 6.87-6.90 (2H, m), 6.95-7.01 (2H, m), 7.13-7.16 (2H, m), 7.19-7.24 (2H, m), 7.26-7.28 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 191(4); Yield: 21.3% (pale orange solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 3.33 (2H, s), 6.18-6.82 (1H, m), 6.96-6.99 (1H, m), 7.03-7.14 (3H, m), 7.20-7.40 (6H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.75 (2H, s), 6.18-6.82 (1H, m), 6.96-6.99 (1H, m), 7.03-7.14 (3H, m), 7.20-7.40 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 2-bromo-4-chloroaniline and 4-(trifluoromethoxy)phenylboronic acid; Yield: 95.3% (brown oil).
1H-NMR (CDCl3) δ: 3.71 (2H, brs), 6.70 (1H, d, J=8.4 Hz), 7.08 (1H, d, J=2.4 Hz), 7.12 (1H, dd, J=2.4, 8.4 Hz), 7.27-7.31 (2H, m), 7.44-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 192(1) and 4-(tert-butyl)benzyl bromide; Yield: 94.3% (brown oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.84 (1H, brs), 4.28 (2H, s), 6.93-6.95 (1H, m), 7.05 (1H, d, J=2.7 Hz), 7.15 (1H, dd, J=2.7, 8.7 Hz), 7.19-7.25 (2H, m), 7.27-7.31 (2H, m), 7.34-7.36 (2H, m), 7.44-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 192(2) and methyl chloroglyoxylate; Yield: 95.6% (yellow oil).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.42 (1H, d, J=14.4 Hz), 3.67 (3H, s), 5.11 (1H, d, J=14.4 Hz), 6.76 (1H, d, J=8.4 Hz), 6.90-6.95 (2H, m), 7.17 (1H, dd, J=2.4, 8.4 Hz), 7.20-7.24 (2H, m), 7.31-7.34 (2H, m), 7.39 (1H, d, J=2.4 Hz), 7.59-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 192(3); Yield: 61.5% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.21 (9H, s), 3.09 (1H, d, J=14.7 Hz), 4.81 (1H, d, J=14.7 Hz), 6.85-6.88 (2H, m), 7.03 (1H, d, J=8.4 Hz), 7.19-7.21 (2H, m), 7.27 (1H, dd, J=2.7, 8.4 Hz), 7.40 (1H, d, J=2.7 Hz), 7.43-7.46 (2H, m), 8.05-8.08 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.21 (9H, s), 3.89-3.94 (1H, m), 4.55-4.61 (1H, m), 6.93-6.97 (2H, m), 7.09-7.12 (2H, m), 7.19-7.46 (5H, m), 8.05-8.08 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 185(1) and 1-butanol; Yield: 87.6% (yellow solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.39-1.46 (2H, m), 1.72-1.81 (2H, m), 4.10 (2H, t, J=6.6 Hz), 7.03 (1H, dd, J=1.5, 7.8 Hz), 7.26-7.30 (2H, m), 7.55-7.58 (2H, m), 8.22-8.26 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 193(1); Yield: 91.9% (brown oil).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=7.2 Hz), 1.31-1.41 (2H, m) 1.58-1.67 (2H, m), 3.48 (2H, brs), 3.83 (2H, t, J=6.3 Hz), 6.64-6.68 (2H, m), 6.82 (1H, d, J=8.4 Hz), 7.20-7.23 (2H, m), 7.53-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 193(2) and methyl chloroglyoxylate; Yield: 78.7% (white solid).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.5 Hz), 1.36-1.43 (2H, m), 1.66-1.73 (2H, m), 3.95-3.99 (5H, m), 6.98 (1H, d, J=8.7 Hz), 7.23-7.27 (2H, m), 7.52 (1H, d, J=2.7 Hz), 7.54-7.57 (2H, m), 7.65 (1H, dd, J=3.0, 8.7 Hz), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 193(3) and 4-(tert-butyl)benzyl bromide; Yield: 76.9% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.36-1.44 (2H, m), 1.66-4.73 (2H, m), 3.57 (3H, s), 3.95 (2H, t, J=6.3 Hz), 4.88 (2H, s), 6.85-6.88 (2H, m), 7.04 (1H, dd, J=2.7, 9.0 Hz), 7.15-7.20 (4H, m), 7.30-7.34 (2H, m), 7.35-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 193(4); Yield: 75.9% (white solid).
1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=7.2 Hz), 1.24 (9H, s), 1.29-1.36 (2H, m), 1.56-1.65 (2H, m), 3.95 (2H, t, J=6.3 Hz), 4.84 (2H, s), 7.02 (1H, d, J=8.7 Hz), 7.09 (1H, d, J=2.4 Hz), 7.12-7.14 (2H, m), 7.19 (1H, dd, J=2.4, 8.7 Hz), 7.28-7.37 (4H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-pentanol; Yield: 74.9% (brown solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.39-1.54 (4H, m), 1.82-1.91 (2H, m), 4.11-4.17 (2H, m), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.55-7.58 (2H, m), 7.70 (1H, dd, J=2.7, 9.0 Hz), 8.02 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 194(1); Yield: 76.8% (yellow solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.37-1.55 (4H, m), 1.80-1.87 (2H, m), 3.89 (2H, brs), 4.01-4.05 (2H, m), 6.82-6.93 (3H, m), 7.21-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 194(2) and methyl chloroglyoxylate; Yield: 84.8% (white solid).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.40-1.52 (4H, m), 1.86-1.95 (2H, m), 3.99 (3H, s), 4.11 (2H, t, J=6.6 Hz), 6.98 (1H, d, J=8.4 Hz), 7.25-7.33 (3H, m), 7.58-7.61 (2H, m), 8.68 (1H, d, J=2.1 Hz), 9.60 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(3) and 4-(tert-butyl)benzyl bromide; Yield: 50.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.28 (9H, s), 1.40-1.49 (4H, m), 1.74-1.81 (2H, m), 3.53 (3H, s), 3.93-3.99 (2H, m), 4.37 (1H, d, J=13.8 Hz), 5.40 (1H, d, J=13.8 Hz), 6.94-6.97 (2H, m), 7.13-7.20 (4H, m), 7.27-7.31 (4H, m), 7.43 (1H, dd, J=2.4, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 194(4); Yield: 80.4% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.90-0.99 (3H, m), 1.21 (9H, s), 1.32-1.50 (4H, m), 1.72-1.78 (2H, m), 3.32-3.40 (1H, m), 4.03-4.07 (2H, m), 4.73-4.78 (1H, m), 7.05-7.09 (3H, m), 7.24-7.27 (2H, m), 7.35-7.38 (3H, m), 7.43-7.46 (1H, m), 7.51-7.54 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.90-0.99 (3H, m), 1.21 (9H, s), 1.32-1.50 (4H, m), 1.72-1.78 (2H, m), 3.96 (2H, t, J=6.3 Hz), 4.21-4.26 (1H, m), 5.22-5.26 (1H, m), 6.94-6.95 (1H, m), 7.05-7.54 (10H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(3) and benzyl bromide; Yield: 30.3% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.34-1.50 (4H, m), 1.75-1.84 (2H, m), 3.54 (3H, s), 3.95-4.00 (2H, m), 4.48 (1H, d, J=14.4 Hz), 5.38 (1H, d, J=14.4 Hz), 6.95 (1H, d, J=8.7 Hz), 7.03 (1H, d, J=2.7 Hz), 7.19-7.29 (7H, m), 7.32-7.35 (2H, m), 7.43 (1H, dd, J=2.7, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 195(1); Yield: 43.4% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.90-0.95 (3H, m), 1.32-1.50 (4H, m), 1.72-1.79 (2H, m), 3.28-3.30 (1H, m), 4.03-4.07 (2H, m), 4.83-4.88 (1H, m), 7.05-7.26 (6H, m), 7.35-7.39 (3H, m), 7.44-7.55 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.90-0.95 (3H, m), 1.32-1.50 (4H, m), 1.72-1.79 (2H, m), 3.97 (2H, t, J=6.3 Hz), 4.21-4.26 (1H, m), 5.22-5.26 (1H, m), 7.02-7.26 (6H, m), 7.35-7.55 (6H, m).
The title compound was obtained in the same manner as the Example 190(3) using the following starting materials.
Starting materials: 2-chloro-5-nitrobenzaldehyde and 4-(trifluoromethoxy)phenylboronic acid;
Yield: 39.3% (yellow oil).
1H-NMR (CDCl3) δ: 7.39-7.48 (4H, m), 7.65 (1H, d, J=8.1 Hz), 8.49 (1H, dd, J=2.4, 8.1 Hz), 8.86 (1H, d, J=2.4 Hz), 10.00 (1H, s).
A solution of triethyl phosphonoacetate (492 mg, 2.19 mmol) in tetrahydrofuran (5 ml) was added dropwise at a slow speed to sodium hydride (95 mg, 2.19 mmol) at room temperature under argon atmosphere, and the mixture was stirred at room temperature for 30 minutes. A solution of the intermediate 196(1) (488 mg, 1.56 mmol) in tetrahydrofuran (3 ml) was added dropwise at a slow speed to this mixture at 0° C., and the mixture was stirred at room temperature for 3 hours. A small amount of saturated aqueous solution of ammonium chloride was added to the reaction mixture. The residue obtained by evaporation of the tetrahydrofuran under reduced pressure was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with methanol to give the title compound (176 mg, 29.6%) as a white solid.
1H-NMR (CDCl3) δ: 1.31 (3H, t, J=7.2 Hz), 4.24 (2H, q, J=7.2 Hz), 6.57 (1H, d, J=16.2 Hz), 7.33-7.38 (4H, m), 7.53 (1H, d, J=8.1 Hz), 7.63 (1H, d, J=16.2 Hz), 8.28 (1H, dd, J=2.4, 8.1 Hz), 8.56 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 196(2); Yield: 96.8% (black oil).
1H-NMR (CDCl3) δ: 1.19 (3H, t, J=7.2 Hz), 2.37-2.42 (2H, m), 2.84 (2H, t, J=8.4 Hz), 3.35 (2H, brs), 4.02-4.10 (2H, m), 6.59 (1H, dd, J=2.4, 8.1 Hz), 6.62 (1H, d, J=2.4 Hz), 6.98 (1H, d, J=8.1 Hz), 7.20-7.23 (2H, m), 7.27-7.31 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 196(3) and methyl chloroglyoxylate; Yield: 80.1% (white solid).
1H-NMR (CDCl3) δ: 1.16-1.25 (3H, m), 2.43 (2H, t, J=7.2 Hz), 2.92 (2H, t, J=7.2 Hz), 3.96-4.10 (5H, m), 7.20 (1H, d, J=8.4 Hz), 7.25-7.33 (4H, m), 7.55-7.61 (2H, m), 8.90 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 196(4) and 4-(tert-butyl)benzyl bromide; Yield: 72.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.18 (3H, t, J=7.2 Hz), 1.30 (9H, s), 2.28 (2H, t, J=7.5 Hz), 2.81 (2H, t, J=7.5 Hz), 3.61 (3H, s), 4.04 (2H, q, J=7.2 Hz), 4.93 (2H, s), 6.93 (1H, d, J=2.1 Hz), 7.00 (1H, dd, J=2.1, 8.1 Hz), 7.13 (1H, d, J=8.1 Hz), 7.17-7.19 (2H, m), 7.27-7.35 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 196(5); Yield: 80.4% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 2.30 (2H, t, J=7.2 Hz), 2.70 (2H, t, J=7.2 Hz), 4.93 (2H, s), 7.11-7.23 (5H, m), 7.34-7.37 (2H, m), 7.40-7.44 (4H, m), 12.12 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 185(1) and 3-pentanol; Yield: 43.4% (yellow oil).
1H-NMR (CDCl3) δ: 0.89 (6H, t, J=7.8 Hz), 1.64-1.70 (4H, m), 4.31-4.35 (1H, m), 6.98-7.01 (1H, m), 7.26-7.29 (2H, m), 7.53-7.56 (2H, m), 8.19-8.23 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 197(1); Yield: 99.9% (black oil).
1H-NMR (CDCl3) δ: 0.78 (6H, t, J=7.2 Hz), 1.44-1.54 (4H, m), 3.48 (2H, brs), 3.81-3.88 (1H, m), 6.62-6.67 (2H, m), 6.80-6.84 (1H, m), 7.19-7.22 (2H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 197(2) and methyl chloroglyoxylate; Yield: 99.3% (brown oil).
1H-NMR (CDCl3) δ: 0.84 (6H, t, J=7.5 Hz), 1.55-1.61 (4H, m), 3.97 (3H, s), 4.09-4.13 (1H, m), 6.96 (1H, d, J=9.0 Hz), 7.21-7.27 (2H, m), 7.49 (1H, d, J=2.7 Hz), 7.53-7.67 (2H, m), 7.63 (1H, dd, J=2.7, 9.0 Hz), 8.79 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 197(3) and 4-(tert-butyl)benzyl bromide; Yield: 84.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.84 (6H, t, J=7.5 Hz), 1.30 (9H, s), 1.55-1.61 (4H, m), 3.56 (3H, s), 4.10-4.14 (1H, m), 4.88 (2H, s), 6.82-6.86 (2H, m), 7.02 (1H, dd, J=2.7, 8.7 Hz), 7.15-7.19 (4H, m), 7.31-7.38 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 197(4); Yield: 81.2% (white solid).
1H-NMR (DMSO-d6) δ: 0.80 (6H, t, J=7.5 Hz), 1.24 (9H, s), 1.50-1.56 (4H, m), 4.17-4.22 (1H, m), 4.78 (2H, s), 6.93-6.97 (1H, m), 7.11-7.19 (4H, m), 7.28-7.36 (4H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 2-bromo-4-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 37.4% (colorless oil).
1H-NMR (CDCl3) δ: 7.10-8.01 (7H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 198(1) and 1-propanol; Yield: 88.2% (yellow oil).
1H-NMR (CDCl3) δ: 1.05 (3H, t, J=7.5 Hz), 1.78-1.92 (2H, m), 4.01 (2H, t, J=6.6 Hz), 6.81 (1H, d, J=2.7 Hz), 6.94 (1H, dd, J=2.7, 9.3 Hz), 7.21-7.35 (4H, m), 8.02 (1H, d, J=9.3 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 198(2); Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 1.02 (3H, t, J=7.5 Hz), 1.71-1.84 (2H, m), 3.45 (2H, brs), 3.87 (2H, t, J=6.6 Hz), 6.71 (1H, d, J=2.7 Hz), 6.72 (1H, d, J=8.7 Hz), 6.79 (1H, dd, J=2.7, 8.7 Hz), 7.26-7.31 (2H, m), 7.46-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 198(3) and methyl chloroglyoxylate; Yield: 41.0% (white solid).
1H-NMR (CDCl3) δ: 1.04 (3H, t, J=7.5 Hz), 1.75-1.88 (2H, m), 3.89 (3H, s), 3.94 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=3.0 Hz), 6.96 (1H, dd, J=3.0, 9.0 Hz), 7.34 (2H, d, J=8.7 Hz), 7.42 (2H, d, J=8.7 Hz), 8.22 (1H, d, J=9.0 Hz), 8.74 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 198(4) and 4-(tert-butyl)benzyl bromide; Yield: 91.3% (colorless oil).
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=6.9 Hz), 1.27 (9H, s), 1.77-2.04 (2H, m), 3.40 (1H, d, J=14.4 Hz), 3.65 (3H, s), 3.91 (2H, t, J=6.6 Hz), 5.07 (1H, d, J=14.4 Hz), 6.67 (1H, dd, J=2.7, 8.4 Hz), 6.74 (1H, d, J=8.4 Hz), 6.89 (1H, d, J=2.7 Hz), 6.90-6.96 (2H, m), 7.18-7.23 (2H, m), 7.26-7.32 (2H, m), 7.59-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 198(5); Yield: 43.5% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.95 (3H, t, J=7.5 Hz), 1.21 (9H, s), 1.64-1.76 (2H, m), 3.05 (1H, d, J=14.7 Hz), 3.91 (2H, t, J=6.3 Hz), 4.78 (1H, d, J=14.7 Hz), 6.72 (1H, dd, J=3.0, 8.4 Hz), 6.82 (1H, d, J=3.0 Hz), 6.86 (2H, d, J=8.4 Hz), 6.94 (1H, d, J=8.4 Hz), 7.17-7.21 (2H, m), 7.37-7.42 (2H, m), 8.04-8.08 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.93-4.55 (18H, m), 6.78-6.91 (5H, m), 7.06-7.10 (2H, m), 7.25-7.29 (2H, m), 7.32-7.36 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 3-pentanol; Yield: 85.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.00 (6H, t, J=7.5 Hz), 1.72-1.81 (4H, m), 4.31-4.35 (1H, m), 7.12 (1H, d, J=8.7 Hz), 7.27-7.31 (2H, m), 7.53-7.58 (2H, m), 7.66 (1H, dd, J=2.1, 8.7 Hz), 7.97 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 199(1); Yield: 84.8% (brown solid).
1H-NMR (CDCl3) δ: 0.99 (6H, t, J=7.5 Hz), 1.68-1.77 (4H, m), 3.89 (2H, brs), 4.16-4.20 (1H, m), 6.81-6.92 (3H, m), 7.21-7.25 (2H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 199(2) and 4-(tert-butyl)benzyl bromide; Yield: 74.5% (colorless oil).
1H-NMR (CDCl3) δ: 0.95-1.04 (6H, m), 1.29 (9H, s), 1.67-1.81 (4H, m), 4.18-4.40 (3H, m), 4.74-4.79 (1H, m), 6.77-6.81 (2H, m), 6.89-6.94 (2H, m), 7.04 (1H, dd, J=2.4, 8.1 Hz), 7.17-7.50 (6H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 199(3) and methyl chloroglyoxylate; Yield: 99.9% (brown oil).
1H-NMR (CDCl3) δ: 0.94-1.02 (6H, m), 1.29 (9H, s), 1.57-1.78 (4H, m), 3.52 (3H, s), 4.22-4.32 (2H, m), 5.46-5.51 (1H, m), 6.92-6.95 (2H, m), 7.13-7.21 (4H, m), 7.26-7.31 (4H, m), 7.41 (1H, dd, J=2.4, 9.0 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 199(4); Yield: 45.9% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.88-0.96 (6H, m), 1.20 (9H, s), 1.57-1.64 (4H, m), 4.26-5.30 (3H, m), 7.06-7.08 (2H, m), 7.23-7.52 (9H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.88-0.96 (6H, m), 1.20 (9H, s), 1.57-1.64 (4H, m), 4.26-5.30 (3H, m), 6.92-7.08 (2H, m), 7.23-7.52 (9H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 96.0% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.59 (3H, s), 4.95 (2H, s), 7.15-7.25 (5H, m), 7.30-7.34 (2H, m), 7.38-7.55 (5H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 200(1); Yield: 58.2% (white solid).
1H-NMR (CDCl3) δ: 1.24 (9H, s), 4.95 (2H, s), 7.17 (2H, d, J=7.8 Hz), 7.31-7.40 (5H, m), 7.58 (1H, t, J=7.8 Hz), 7.60-7.63 (1H, m), 7.68-7.74 (3H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 2-(trifluoromethoxy)phenylboronic acid; Yield: 88.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.53 (3H, s), 4.96 (2H, s), 7.11-7.20 (4H, m), 7.29-7.44 (8H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 201(1); Yield: 59.5% (white solid).
1H-NMR (CDCl3) δ: 1.24 (9H, s), 4.95 (2H, s), 7.13 (2H, d, J=7.8 Hz), 7.29-7.35 (4H, m), 7.44-7.55 (6H, m).
The title compound was obtained in the same manner as the Example 190(3) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-(tert-butyl)phenylboronic acid; Yield: 47.5% (gray solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 3.99 (3H, s), 7.45-7.54 (4H, m), 7.59-7.72 (4H, m), 8.88 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 202(1) and 2-(trifluoromethoxy)benzyl bromide; Yield: 91.1% (colorless oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.58 (3H, s), 5.10 (2H, s), 7.11-7.21 (3H, m), 7.27-7.35 (2H, m), 7.43-7.54 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 202(2); Yield: 68.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 5.06 (2H, s), 7.27-7.49 (8H, m), 7.54-7.59 (2H, m), 7.62-7.67 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 202(1) and 3-(trifluoromethoxy)benzyl bromide; Yield: 82.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.57 (3H, s), 4.99 (2H, s), 7.07-7.17 (4H, m), 7.22-7.27 (1H, m), 7.35 (1H, t, J=7.8 Hz), 7.44-7.56 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 203(1); Yield: 69.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 5.04 (2H, s), 7.18-7.21 (1H, m), 7.24-7.32 (4H, m), 7.45-7.51 (3H, m), 7.54-7.60 (2H, m), 7.63-7.69 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 202(1) and 4-chlorobenzyl chloride; Yield: 51.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.56 (3H, s), 4.93 (2H, s), 7.06-7.11 (2H, m), 7.17-7.22 (2H, m), 7.25-7.29 (2H, m), 7.44-7.55 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 204(1); Yield: 71.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.97 (2H, s), 7.24-7.29 (4H, m), 7.37-7.43 (2H, m), 7.44-7.49 (2H, m), 7.55-7.60 (2H, m), 7.63-7.69 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 202(1) and 4-(trifluoromethyl)benzyl chloride; Yield: 52.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 3.58 (3H, s), 5.02 (2H, s), 7.09-7.14 (2H, m), 7.37-7.41 (2H, m), 7.44-7.59 (8H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 205(1); Yield: 73.6% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 5.08 (2H, s), 7.31 (2H, d, J=8.4 Hz), 7.44-7.50 (4H, m), 7.54-7.60 (2H, m), 7.67 (2H, d, J=8.4 Hz), 7.72 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 202(1) and the intermediate 167(1); Yield: 32.8% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.5 Hz), 1.22-1.41 (11H, m), 1.52-1.62 (2H, m), 2.58 (2H, t, J=7.8 Hz), 3.55 (3H, s), 4.93 (2H, s), 7.08-7.17 (6H, m), 7.43-7.53 (6H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 206(1); Yield: 58.8% (white solid).
1H-NMR (DMSO-d6) δ: 0.87 (3H, t, J=7.5 Hz), 1.21-1.34 (11H, m), 1.46-1.56 (2H, m), 2.53 (2H, t, J=7.5 Hz), 4.93 (2H, s), 7.09-7.16 (4H, m), 7.23-7.28 (2H, m), 7.43-7.49 (2H, m), 7.54-7.60 (2H, m), 7.61-7.67 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 198(1) and 3-pentanol; Yield: 91.4% (brown oil).
1H-NMR (CDCl3) δ: 0.96 (6H, t, J=7.2 Hz), 1.68-1.77 (4H, m), 4.24-4.27 (1H, m), 6.80 (1H, d, J=2.7 Hz), 6.92 (1H, dd, J=2.7, 9.0 Hz), 7.24-7.35 (4H, m), 8.01 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 207(1); Yield: 96.3% (brown oil).
1H-NMR (CDCl3) δ: 0.96 (6H, t, J=7.5 Hz), 1.61-1.70 (4H, m), 3.46 (2H, brs), 3.94-3.99 (1H, m), 6.69-6.72 (2H, m), 6.79 (1H, dd, J=2.7, 8.7 Hz), 7.26-7.30 (2H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 207(2) and methyl chloroglyoxylate; Yield: 91.0% (brown oil).
1H-NMR (CDCl3) δ: 0.96 (6H, t, J=7.5 Hz), 1.64-1.71 (4H, m), 3.89 (3H, s), 4.11-4.15 (1H, m), 6.83 (1H, d, J=3.0 Hz), 6.96 (1H, dd, J=3.0, 9.0 Hz), 7.33-7.36 (2H, m), 7.40-7.43 (2H, m), 8.20 (1H, d, J=9.0 Hz), 8.74 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 207(3) and 4-(tert-butyl)benzyl bromide; Yield: 94.9% (colorless oil).
1H-NMR (CDCl3) δ: 0.92-0.97 (6H, m), 1.26 (9H, s), 1.62-1.70 (4H, m), 3.42 (1H, d, J=14.4 Hz), 3.64 (3H, s), 4.08-4.15 (1H, m), 5.05 (1H, d, J=14.4 Hz), 6.66 (1H, dd, J=2.7, 8.7 Hz), 6.75 (1H, d, J=8.7 Hz), 6.88 (1H, d, J=2.7 Hz), 6.93-6.96 (2H, m), 7.18-7.22 (2H, m), 7.25-7.33 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 207(4); Yield: 76.1% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.91 (6H, m), 1.18-1.21 (9H, m), 1.55-1.62 (4H, m), 3.07 (1H, d, J=14.7 Hz), 4.17-4.24 (1H, m), 4.76 (1H, d, J=14.7 Hz), 6.72 (1H, dd, J=2.7, 8.7 Hz), 6.80 (1H, d, J=2.7 Hz), 6.86-6.88 (2H, m), 6.96 (1H, d, J=8.7 Hz), 7.17-7.20 (2H, m), 7.39-7.41 (2H, m), 8.04-8.07 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.91 (6H, m), 1.18-1.21 (9H, m), 1.55-1.62 (4H, m), 3.79-3.86 (1H, m), 4.17-4.24 (1H, m), 4.47-4.44 (1H, m), 6.77-6.98 (3H, m), 7.07-7.41 (6H, m), 8.04-8.07 (2H, m).
A mixture of the intermediate 198(1) (700 mg, 2.32 mmol), diethylamine (339 mg, 4.64 mmol), potassium carbonate (320 mg, 2.32 mmol) and acetonitrile (5 ml) was stirred at 100° C. for 10 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (580 mg, 70.5%) as a yellow solid.
1H-NMR (CDCl3) δ: 1.22 (6H, t, J=6.9 Hz), 3.45 (4H, q, J=6.9 Hz), 6.37 (1H, d, J=3.0 Hz), 6.60 (1H, dd, J=3.0, 9.0 Hz), 7.23-7.33 (4H, m), 8.08 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 208(1); Yield: 87.5% (yellow solid).
1H-NMR (CDCl3) δ: 1.11 (6H, t, J=6.9 Hz), 3.24 (4H, q, J=6.9 Hz), 3.35 (2H, brs), 6.57 (1H, d, J=2.7 Hz), 6.66-6.75 (2H, m), 7.26-7.29 (2H, m), 7.48-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 208(2) and methyl chloroglyoxylate; Yield: 89.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.17 (6H, t, J=6.9 Hz), 3.37 (4H, q, J=6.9 Hz), 3.88 (3H, s), 6.53 (1H, d, J=3.0 Hz), 6.72 (1H, dd, J=3.0, 9.0 Hz), 7.31-7.34 (2H, m), 7.37-7.43 (2H, m), 8.08 (1H, d, J=9.0 Hz), 8.63 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 208(3) and 4-(tert-butyl)benzyl bromide; Yield: 90.7% (yellow oil).
1H-NMR (CDCl3) δ: 1.16 (6H, t, J=7.2 Hz), 1.27 (9H, s), 3.30-3.39 (5H, m), 3.65 (3H, s), 5.00 (1H, d, J=14.4 Hz), 6.40 (1H, dd, J=3.0, 9.0 Hz), 6.54 (1H, d, J=3.0 Hz), 6.68 (1H, d, J=9.0 Hz), 6.96-6.99 (2H, m), 7.19-7.22 (2H, m), 7.25-7.30 (2H, m), 7.60-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 208(4); Yield: 75.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.06 (6H, t, J=7.2 Hz), 1.22 (9H, s), 3.31-3.36 (5H, m), 4.80 (1H, d, J=14.4 Hz), 6.53-6.56 (2H, m), 6.76-6.78 (1H, m), 6.92-6.94 (2H, m), 7.23-7.36 (2H, m), 7.46-7.48 (2H, m), 7.71-7.74 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 198(1) and 2-propanol; Yield: 99.9% (yellow oil).
1H-NMR (CDCl3) δ: 1.39 (6H, d, J=6.0 Hz), 4.63-4.69 (1H, m), 6.79 (1H, d, J=2.7 Hz), 6.92 (1H, dd, J=2.7, 9.0 Hz), 7.24-7.34 (4H, m), 8.01 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 209(1); Yield: 92.1% (yellow oil).
1H-NMR (CDCl3) δ: 1.24-1.34 (6H, m), 3.47 (2H, brs), 4.36-4.44 (1H, m), 6.69-6.72 (2H, m), 6.78 (1H, dd, J=2.7, 8.7 Hz), 7.25-7.30 (2H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 209(2) and methyl chloroglyoxylate; Yield: 74.0% (yellow solid).
1H-NMR (CDCl3) δ: 1.35 (6H, d, J=6.0 Hz), 3.89 (3H, s), 4.52-4.60 (1H, m), 6.82 (1H, d, J=3.0 Hz), 6.95 (1H, dd, J=3.0, 9.0 Hz), 7.33-7.36 (2H, m), 7.39-7.43 (2H, m), 8.21 (1H, d, J=9.0 Hz), 8.74 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 209(3) and 4-(tert-butyl)benzyl bromide; Yield: 99.9% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (9H, s), 1.32-1.35 (6H, m), 3.40 (1H, d, J=14.4 Hz), 3.65 (3H, s), 4.50-4.56 (1H, m), 5.06 (1H, d, J=14.4 Hz), 6.65 (1H, dd, J=2.7, 8.7 Hz), 6.74 (1H, d, J=8.7 Hz), 6.86 (1H, d, J=2.7 Hz), 6.92-6.95 (2H, m), 7.19-7.22 (2H, m), 7.28-7.31 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 209(4); Yield: 40.1% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.15-1.27 (15H, m), 3.03 (1H, d, J=14.7 Hz), 4.56-4.64 (1H, m), 4.76 (1H, d, J=14.7 Hz), 6.70 (1H, dd, J=3.0, 8.7 Hz), 6.78 (1H, d, J=3.0 Hz), 6.84-6.87 (2H, m), 6.94 (1H, d, J=8.7 Hz), 7.17-7.20 (2H, m), 7.38-7.41 (2H, m), 8.05-8.08 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.15-1.27 (15H, m), 3.78-3.82 (1H, m), 4.47-4.51 (1H, m), 4.56-4.64 (1H, m), 6.70 (1H, dd, J=3.0, 8.7 Hz), 6.76-6.78 (1H, m), 6.84-6.87 (2H, m), 6.94 (1H, d, J=8.7 Hz), 7.07-7.41 (4H, m), 8.05-8.08 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 185(3) and methyl chloroglyoxylate; Yield: 75.3% (white solid).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.68-1.81 (2H, m), 3.93 (2H, t, J=6.3 Hz), 3.97 (3H, s), 6.97 (1H, d, J=9.0 Hz), 7.22-7.27 (2H, m), 7.52 (1H, d, J=2.4 Hz), 7.54-7.59 (2H, m), 7.65 (1H, dd, J=2.4, 9.0 Hz), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 210(1) and benzyl bromide; Yield: 80.3% (colorless oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.2 Hz), 1.68-1.77 (2H, m), 3.58 (3H, s), 3.90 (2H, t, J=6.3 Hz), 4.92 (2H, s), 6.82-6.85 (1H, m), 6.96-7.00 (2H, m), 7.19-7.33 (7H, m), 7.39-7.42 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 210(2); Yield: 57.1% (white solid).
1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=7.2 Hz), 1.60-1.67 (2H, m), 3.88-3.92 (2H, m), 4.84 (2H, s), 6.93-7.04 (2H, m), 7.15-7.30 (6H, m), 7.36-7.38 (2H, m), 7.54-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 3-bromo-4-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 70.8% (white solid).
1H-NMR (CDCl3) δ: 7.30-7.37 (3H, m), 7.60-7.63 (2H, m), 8.23-8.29 (1H, m), 8.36-8.39 (1H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and 2-propanol; Yield: 99.9% (yellow solid).
1H-NMR (CDCl3) δ: 1.36 (6H, d, J=6.0 Hz), 4.68-4.76 (1H, m), 7.01-7.04 (1H, m), 7.25-7.29 (2H, m), 7.54-7.59 (2H, m), 8.20-8.24 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 211(2); Yield: 99.9% (brown oil).
1H-NMR (CDCl3) δ: 1.13 (6H, d, J=6.0 Hz), 3.50 (2H, brs), 4.06-4.14 (1H, m), 6.62-6.67 (2H, m), 6.85 (1H, d, J=8.7 Hz), 7.20-7.23 (2H, m), 7.53-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 211(3) and methyl chloroglyoxylate; Yield: 73.2% (purple solid).
1H-NMR (CDCl3) δ: 1.25 (6H, d, J=6.0 Hz), 3.97 (3H, s), 4.41-4.49 (1H, m), 6.99 (1H, d, J=8.7 Hz), 7.22-7.27 (2H, m), 7.51 (1H, d, J=2.7 Hz), 7.55-7.59 (2H, m), 7.64 (1H, dd, J=2.7, 8.7 Hz), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 211(4) and 4-(tert-butyl)benzyl bromide; Yield: 89.1% (brown solid).
1H-NMR (CDCl3) δ: 1.25-1.33 (15H, m), 3.56 (3H, s), 4.46-4.54 (1H, m), 4.88 (2H, s), 6.86-6.88 (2H, m), 7.03 (1H, dd, J=2.7, 8.7 Hz), 7.16-7.19 (4H, m), 7.31-7.34 (2H, m), 7.35-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 211(5); Yield: 44.1% (white solid).
1H-NMR (DMSO-d6) δ: 1.20-1.24 (15H, m), 4.57-4.65 (1H, m), 4.87 (2H, s), 7.01 (1H, d, J=2.4 Hz), 7.10-7.19 (4H, m), 7.34-7.38 (4H, m), 7.46-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and benzylalcohol; Yield: 81.4% (white solid).
1H-NMR (CDCl3) δ: 5.23 (2H, s), 7.09 (1H, d, J=9.0 Hz), 7.26-7.37 (7H, m), 7.58-7.61 (2H, m), 8.20-8.25 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 212(1); Yield: 94.1% (yellowish-brown oil).
1H-NMR (CDCl3) δ: 3.51 (2H, brs), 4.91 (2H, s), 6.60-6.69 (2H, m), 6.89 (1H, d, J=8.7 Hz), 7.21-7.32 (7H, m), 7.54-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 212(2) and methyl chloroglyoxylate; Yield: 78.4% (pale orange solid).
1H-NMR (CDCl3) δ: 3.97 (3H, s), 5.08 (2H, s), 7.04 (1H, d, J=9.0 Hz), 7.26-7.36 (7H, m), 7.54-7.66 (4H, m), 8.81 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 212(3) and 4-(tert-butyl)benzyl bromide; Yield: 70.1% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.55 (3H, s), 4.88 (2H, s), 5.07 (2H, s), 6.89 (1H, d, J=3.0 Hz), 6.94 (1H, d, J=8.7 Hz), 7.04 (1H, dd, J=3.0, 8.7 Hz), 7.14-7.19 (4H, m), 7.24-7.41 (9H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 212(4); Yield: 47.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 4.89 (2H, s), 5.13 (2H, s), 7.04-7.24 (5H, m), 7.32-7.38 (9H, m), 7.49-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and diethylamine; Yield: 40.1% (yellow oil).
1H-NMR (CDCl3) δ: 0.97 (6H, t, J=7.2 Hz), 3.04 (4H, q, J=7.2 Hz), 7.02 (1H, d, J=9.0 Hz), 7.26-7.03 (2H, m), 7.51-7.56 (2H, m), 8.03 (1H, d, J=2.7 Hz), 8.12 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 213(1); Yield: 95.1% (yellowish-green oil).
1H-NMR (CDCl3) δ: 0.85 (6H, t, J=7.2 Hz), 2.76 (4H, q, J=7.2 Hz), 3.53 (2H, brs), 6.60-6.67 (2H, m), 6.97 (1H, d, J=8.4 Hz), 7.17-7.20 (2H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 213(2) and methyl chloroglyoxylate; Yield: 85.6% (pale green solid).
1H-NMR (CDCl3) δ: 0.89 (6H, t, J=7.2 Hz), 2.85 (4H, q, J=7.2 Hz), 3.97 (3H, s), 7.09 (1H, d, J=8.7 Hz), 7.21-7.24 (2H, m), 7.41 (1H, d, J=2.7 Hz), 7.56-7.59 (2H, m), 7.62 (1H, dd, J=2.7, 8.7 Hz), 8.79 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 213(3) and 4-(tert-butyl)benzyl bromide; Yield: 88.1% (colorless oil).
1H-NMR (CDCl3) δ: 0.86 (6H, t, J=7.2 Hz), 1.29 (9H, s), 2.83 (4H, q, J=7.2 Hz), 3.54 (3H, s), 4.88 (2H, s), 6.77 (1H, d, J=2.4 Hz), 6.96-6.97 (2H, m), 7.15-7.18 (4H, m), 7.29-7.33 (2H, m), 7.38-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 213(4); Yield: 64.7% (white solid).
1H-NMR (DMSO-d6) δ: 0.79 (6H, t, J=7.2 Hz), 1.23 (9H, s), 2.78 (4H, q, J=7.2 Hz), 4.87 (2H, s), 6.88 (1H, d, J=2.1 Hz), 7.07-7.14 (4H, m), 7.32-7.38 (4H, m), 7.48-7.50 (2H, m), 13.93 (1H, brs).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and dimethylamine hydrochloride; Yield: 99.9% (yellow solid).
1H-NMR (CDCl3) δ: 2.71 (6H, s), 6.95 (1H, d, J=9.0 Hz), 7.26-7.30 (2H, m), 7.50-7.55 (2H, m), 8.06 (1H, d, J=3.0 Hz), 8.13 (1H, dd, J=3.0, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 214(1); Yield: 99.9% (blue oil).
1H-NMR (CDCl3) δ: 2.44 (6H, s), 3.50 (2H, brs), 6.60 (1H, d, J=2.7 Hz), 6.65 (1H, dd, J=2.7, 8.7 Hz), 6.94 (1H, d, J=8.7 Hz), 7.19-7.22 (2H, m), 7.56-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 214(2) and methyl chloroglyoxylate; Yield: 82.1% (green solid).
1H-NMR (CDCl3) δ: 2.54 (6H, s), 3.97 (3H, s), 7.05 (1H, d, J=8.7 Hz), 7.23-7.26 (2H, m), 7.40 (1H, d, J=2.7 Hz), 7.56-7.63 (3H, m), 8.78 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 214(3) and 4-(tert-butyl)benzyl bromide; Yield: 66.8% (brown oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.51 (6H, s), 3.56 (3H, s), 4.86 (2H, s), 6.74 (1H, d, J=2.7 Hz), 6.89 (1H, d, J=8.4 Hz), 6.98 (1H, dd, J=2.7, 8.4 Hz), 7.16-7.20 (4H, m), 7.30-7.33 (2H, m), 7.40-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 214(4); Yield: 85.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.45 (6H, s), 4.85 (2H, s), 6.87 (1H, d, J=2.7 Hz), 7.03 (1H, d, J=8.7 Hz), 7.10-7.15 (3H, m), 7.32-7.35 (2H, m), 7.37-7.40 (2H, m), 7.50-7.53 (2H, m), 13.88 (1H, brs).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 5-bromo-4-fluoro-2-methyl-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 97.9% (orange solid).
1H-NMR (CDCl3) δ: 2.67 (3H, s), 7.15 (1H, d, J=10.8 Hz), 7.31-7.35 (2H, m), 7.57-7.61 (2H, m), 8.17 (1H, d, J=7.5 Hz).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 215(1) and dimethylamine hydrochloride; Yield: 99.9% (yellow solid).
1H-NMR (CDCl3) δ: 2.68 (9H, s), 6.75 (1H, s), 7.24-7.29 (2H, m), 7.45-7.54 (2H, m), 7.99 (1H, s).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 215(2); Yield: 93.5% (pale yellow oil).
1H-NMR (CDCl3) δ: 2.21 (3H, s), 2.48 (6H, s), 3.55 (2H, brs), 6.58 (1H, s), 6.89 (1H, s), 7.18-7.29 (2H, m), 7.52-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 215(3) and methyl chloroglyoxylate; Yield: 70.2% (white solid).
1H-NMR (DMSO-d6) δ: 2.19 (3H, s), 2.48 (6H, s), 3.84 (3H, s), 6.97 (1H, s), 7.11 (1H, s), 7.37-7.42 (2H, m), 7.60-7.65 (2H, m), 10.26 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 215(4) and 4-(tert-butyl)benzyl bromide; Yield: 77.2% (white solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 2.20 (3H, s), 2.50 (6H, s), 3.51 (3H, s), 4.12 (1H, d, J=13.8 Hz), 5.40 (1H, d, J=13.8 Hz), 6.38 (1H, s), 6.78 (1H, s), 7.09-7.16 (4H, m), 7.23-7.31 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 215(5); Yield: 52.6% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 2.17 (3H, s), 2.45 (6H, s), 4.14 (1H, d, J=13.8 Hz), 5.24 (1H, d, J=13.8 Hz), 6.37 (1H, s), 6.92 (1H, s), 7.08-7.14 (2H, m), 7.27-7.42 (6H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 1.98 (3H, s), 2.44 (6H, s), 4.38-4.47 (1H, m), 4.83-4.92 (1H, m), 6.40 (1H, s), 6.88 (1H, s), 7.08-7.42 (8H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and morpholine; Yield: 67.9% (yellow solid).
1H-NMR (CDCl3) δ: 2.92-2.96 (4H, m), 3.59-3.64 (4H, m), 7.05 (1H, d, J=9.0 Hz), 7.30-7.34 (2H, m), 7.63-7.69 (2H, m), 8.09 (1H, d, J=2.7 Hz), 8.18 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 216(1); Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 2.69-2.73 (4H, m), 3.45-3.60 (6H, m), 6.62 (1H, d, J=2.7 Hz), 6.67 (1H, dd, J=2.7, 8.4 Hz), 6.92 (1H, d, J=8.4 Hz), 7.19-7.25 (2H, m), 7.60-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 216(2) and methyl chloroglyoxylate; Yield: 76.1% (pale yellow solid).
1H-NMR (CDCl3) δ: 2.76-2.81 (4H, m), 3.56-3.61 (4H, m), 3.97 (3H, s), 7.05 (1H, d, J=9.0 Hz), 7.24-7.28 (2H, m), 7.46 (1H, d, J=2.7 Hz), 7.62-7.70 (3H, m), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 216(3) and 4-(tert-butyl)benzyl bromide; Yield: 55.8% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.75-2.79 (4H, m), 3.56-3.60 (7H, m), 4.88 (2H, s), 6.79 (1H, d, J=2.7 Hz), 6.92 (1H, d, J=8.4 Hz), 7.04 (1H, dd, J=2.7, 8.4 Hz), 7.12-7.24 (4H, m), 7.29-7.35 (2H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 216(4); Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.66-2.75 (4H, m), 3.45-3.51 (4H, m), 4.88 (2H, s), 6.95 (1H, d, J=2.4 Hz), 7.06 (1H, d, J=8.7 Hz), 7.11-7.21 (3H, m), 7.32-7.44 (4H, m), 7.62-7.67 (2H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and piperidine; Yield: 85.4% (yellow solid).
1H-NMR (CDCl3) δ: 1.43-1.54 (6H, m), 2.85-2.98 (4H, m), 7.02 (1H, d, J=9.0 Hz), 7.27-7.32 (2H, m), 7.61-7.67 (2H, m), 8.05 (1H, d, J=2.7 Hz), 8.15 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 217(1); Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 1.35-1.52 (6H, m), 2.51-2.75 (4H, m), 3.50 (2H, brs), 6.60-6.66 (2H, m), 6.91 (1H, d, J=8.4 Hz), 7.17-7.24 (2H, m), 7.62-7.67 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 217(2) and methyl chloroglyoxylate; Yield: 76.5% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.40-1.50 (6H, m), 2.69-2.82 (4H, m), 3.96 (3H, s), 7.04 (1H, d, J=8.7 Hz), 7.22-7.26 (2H, m), 7.41 (1H, d, J=2.4 Hz), 7.61 (1H, dd, J=2.4, 8.7 Hz), 7.64-7.70 (2H, m), 8.78 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 217(3) and 4-(tert-butyl)benzyl bromide; Yield: 56.9% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 1.39-1.50 (6H, m), 2.65-2.79 (4H, m), 3.56 (3H, s), 4.87 (2H, s), 6.76 (1H, d, J=2.7 Hz), 6.90 (1H, d, J=8.7 Hz), 6.99 (1H, dd, J=2.7, 8.7 Hz), 7.15-7.20 (4H, m), 7.29-7.34 (2H, m), 7.46-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 217(4); Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 1.32-1.41 (6H, m), 2.60-2.72 (4H, m), 4.87 (2H, s), 6.91 (1H, d, J=2.4 Hz), 7.03 (1H, d, J=8.7 Hz), 7.11-7.16 (3H, m), 7.31-7.41 (4H, m), 7.58-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and tert-butanol; Yield: 100.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 7.23 (1H, d, J=9.0 Hz), 7.26-7.30 (2H, m), 7.56-7.59 (2H, m), 8.16 (1H, dd, J=2.7, 9.0 Hz), 8.24 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 218(1); Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 1.02 (9H, s), 3.56 (2H, brs), 6.60 (1H, dd, J=2.7, 8.4 Hz), 6.67 (1H, d, J=2.7 Hz), 6.93 (1H, d, J=8.4 Hz), 7.20-7.23 (2H, m), 7.54-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 218(2) and methyl chloroglyoxylate; Yield: 83.8% (white solid).
1H-NMR (CDCl3) δ: 1.11 (9H, s), 3.98 (3H, s), 7.13-7.16 (1H, m), 7.23-7.27 (2H, m), 7.56-7.61 (4H, m), 8.83 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 218(3) and 4-(tert-butyl)benzyl bromide; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 1.10 (9H, s), 1.29 (9H, s), 3.54 (3H, s), 4.91 (2H, s), 6.90 (1H, d, J=2.7 Hz), 6.99 (1H, dd, J=2.7, 8.7 Hz), 7.05 (1H, d, J=8.7 Hz), 7.14-7.20 (4H, m), 7.29-7.34 (2H, m), 7.36-7.40 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 218(4); Yield: 77.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.05 (9H, s), 1.23 (9H, s), 4.81 (2H, s), 7.00-7.03 (2H, m), 7.10-7.29 (5H, m), 7.34-7.36 (2H, m), 7.49-7.52 (2H, m).
5-Bromovaleryl chloride (3.89 ml, 19.51 mmol) was added to a solution of 2-chloro-4-nitroaniline (2.59 g, 15.00 mmol) in dimethylacetamide (10 ml) at 0° C., and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate. The organic layer was washed with water, a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (4.64 g, 92.2%) as a white solid.
1H-NMR (CDCl3) δ: 1.93-2.00 (4H, m), 2.56 (2H, t, J=7.2 Hz), 3.47 (2H, t, J=6.0 Hz), 7.87 (1H, brs), 8.18 (1H, dd, J=2.7, 9.0 Hz), 8.31 (1H, d, J=2.7 Hz), 8.70 (1H, d, J=9.0 Hz).
A mixture of the intermediate 219(1) (4.64 g, 13.82 mmol), potassium carbonate (3.82 g, 27.65 mmol) and dimethylformamide (40 ml) was stirred at room temperature for 2 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane and diisopropyl ether to give the title compound (3.20 g, 90.9%) as a white solid.
1H-NMR (CDCl3) δ: 1.93-2.02 (4H, m), 2.58-2.63 (2H, m), 3.52-3.63 (2H, m), 7.46 (1H, d, J=8.4 Hz), 8.19 (1H, dd, J=2.7, 8.4 Hz), 8.38 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 190(3) using the following starting materials.
Starting materials: the intermediate 219(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 62.6% (orange solid).
1H-NMR (CDCl3) δ: 1.74-1.84 (4H, m), 2.34-2.52 (2H, m), 2.98-3.06 (1H, m), 3.34-3.42 (1H, m), 7.29-7.33 (2H, m), 7.41-7.48 (3H, m), 8.27-8.31 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 219(3); Yield: 90.4% (green solid).
1H-NMR (CDCl3) δ: 1.32-1.80 (4H, m), 2.27-2.54 (2H, m), 2.85-2.93 (1H, m), 3.25-3.34 (1H, m), 3.78 (2H, brs), 6.66-6.73 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.20-7.23 (2H, m), 7.36-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 219(4) and methyl chloroglyoxylate; Yield: 80.3% (white solid).
1H-NMR (CDCl3) δ: 1.37-1.81 (4H, m), 2.30-2.39 (1H, m), 2.47-2.55 (1H, m), 2.90-2.95 (1H, m), 3.29-3.36 (1H, m), 3.98 (3H, s), 7.22-7.27 (3H, m), 7.36-7.41 (2H, m), 7.63 (1H, d, J=2.1 Hz), 7.71 (1H, dd, J=2.1, 8.4 Hz), 9.05 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 219(5) and 4-(tert-butyl)benzyl bromide; Yield: 96.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.25-1.70 (13H, m), 2.30-2.52 (2H, m), 2.90-2.96 (1H, m), 3.27-3.33 (1H, m), 3.60 (3H, s), 4.81-4.86 (1H, m), 5.00-5.05 (1H, m), 7.01 (1H, d, J=2.1 Hz), 7.17-7.27 (8H, m), 7.30-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 219(6); Yield: 78.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.24-1.70 (13H, m), 2.10-2.32 (2H, m), 2.50-2.89 (2H, m), 4.92-4.98 (2H, m), 7.15-7.20 (3H, m), 7.29-7.37 (6H, m), 7.42-7.45 (2H, m), 14.24 (1H, brs).
A mixture of 4-(tert-butyl)benzaldehyde (811 mg, 5.00 mmol), 4-bromoaniline (860 mg, 5.00 mmol) and ethanol (10 ml) was refluxed for 7 hours. The reaction mixture was cooled to room temperature. The precipitated solid was collected by filtration, and washed with methanol to give the title compound (1.08 g, 68.0%) as a pale yellow solid.
1H-NMR (DMSO-d6) δ: 1.32 (9H, s), 7.19-7.24 (2H, m), 7.55 (2H, d, J=8.4 Hz), 7.58-7.61 (2H, m), 7.86 (2H, d, J=8.4 Hz), 8.59 (1H, s).
Methyllithium (1.2 M solution in diethyl ether; 1.98 ml, 2.37 mmol) was added to a solution of the intermediate 220(1) (500 mg, 1.58 mmol) in diethyl ether (5 ml) at −10° C. under argon atmosphere, and the mixture was stirred at −10° C. for 3 hours. A saturated aqueous solution of ammonium chloride was added to the reaction mixture at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (209 mg, 39.8%) as a brown oil.
1H-NMR (CDCl3) δ: 1.30 (9H, s), 1.50 (3H, d, J=6.9 Hz), 4.04 (1H, brs), 4.42 (1H, brs), 6.38-6.41 (2H, m), 7.14-7.17 (2H, m), 7.23-7.26 (2H, m), 7.31-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 220(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 67.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.53 (3H, d, J=6.9 Hz), 4.14 (1H, brs), 4.52 (1H, q, J=6.9 Hz), 6.58-6.62 (2H, m), 7.18-7.22 (2H, m), 7.27-7.37 (6H, m), 7.45-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 220(3) and methyl chloroglyoxylate; Yield: 78.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.52 (3H, d, J=7.2 Hz), 3.50 (3H, s), 6.13 (1H, q, J=7.2 Hz), 6.90-6.91 (2H, m), 7.20 (2H, d, J=8.7 Hz), 7.26-7.34 (4H, m), 7.42 (2H, d, J=8.7 Hz), 7.55-7.78 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 220(4); Yield: 50.9% (brown solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 1.35 (3H, s), 5.59 (1H, brs), 6.99 (2H, brs), 7.25-7.34 (4H, m), 7.42 (2H, d, J=8.4 Hz), 7.50 (2H, d, J=8.4 Hz), 7.75 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 220(2) using the following starting materials.
Starting materials: the intermediate 220(1) and n-butyllithium; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.23-1.42 (13H, m), 1.72-1.80 (2H, m), 4.06 (1H, brs), 4.21 (1H, t, J=6.9 Hz), 6.36-6.41 (2H, m), 7.11-7.17 (2H, m), 7.20 (2H, d, J=8.4 Hz), 7.31 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 221(1) and methyl chloroglyoxylate; Yield: 86.9% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.22-1.43 (13H, m), 1.80-1.90 (2H, m), 3.49 (3H, s), 5.89 (1H, t, J=8.1 Hz), 6.52-6.68 (2H, m), 7.04-7.08 (2H, m), 7.26-7.30 (2H, m), 7.33 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 221(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 77.9% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.23-1.52 (13H, m), 1.84-1.89 (2H, m), 3.48 (3H, s), 5.93 (1H, t, J=8.1 Hz), 6.79-6.90 (2H, m), 7.09-7.14 (2H, m), 7.24-7.32 (4H, m), 7.41 (2H, d, J=8.7 Hz), 7.54-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 221(3); Yield: 89.6% (white solid).
1H-NMR (DMSO-d6) δ: 0.85-0.87 (3H, t, J=7.2 Hz), 1.21-1.44 (13H, m), 1.80-1.88 (2H, m), 5.71 (1H, t, J=8.1 Hz), 6.89-6.93 (2H, m), 7.13 (2H, d, J=8.4 Hz), 7.35 (2H, d, J=8.4 Hz), 7.44 (2H, d, J=8.1 Hz), 7.64 (2H, d, J=8.7 Hz), 7.76-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 220(2) using the following starting materials.
Starting materials: the intermediate 220(1) and phenyllithium; Yield: 79.9% (yellow solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 4.24-4.29 (1H, m), 5.42 (1H, d, J=3.0 Hz), 6.37-6.45 (2H, m), 7.11-7.43 (11H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 222(1) and methyl chloroglyoxylate; Yield: 75.9% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.56 (3H, s), 6.73-6.78 (2H, m), 7.04-7.35 (12H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 222(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 72.4% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.55 (3H, s), 6.96-7.00 (2H, m), 7.07 (1H, s), 7.16 (2H, d, J=8.4 Hz), 7.22-7.34 (11H, m), 7.47-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 222(3); Yield: 42.1% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 6.78 (1H, s), 7.08-7.44 (13H, m), 7.57 (2H, d, J=8.4 Hz), 7.69-7.75 (2H, m).
n-Butyllithium (2.5 M solution in hexane; 2.2 ml, 5.5 mmol) was added to a solution of 4-bromoaniline (1.03 g, 6.0 mmol) in tetrahydrofuran at −78° C. under argon atmosphere, and the mixture was stirred for 30 minutes. 2-Phenyethyl bromide (925 mg, 5.0 mmol) was added to the reaction mixture, and the mixture was stirred at room temperature for 1 hour. A saturated aqueous solution of ammonium chloride was added to the reaction mixture. Tetrahydrofuran was evaporated under reduced pressure, and the obtained residue was diluted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (126 mg, 9%) as a colorless oil.
1H-NMR (CDCl3) δ: 2.90 (2H, t, J=6.9 Hz), 3.37 (2H, t, J=6.9 Hz), 3.68 (1H, brs), 6.45-6.52 (2H, m), 7.21-7.37 (7H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 223(1) and methyl chloroglyoxylate; Yield: 99% (pale brown oil).
1H-NMR (CDCl3) δ: 2.87-2.94 (2H, m), 3.58 (3H, s), 3.94-4.02 (2H, m), 6.91-6.96 (2H, m), 7.13-7.32 (5H, m), 7.44-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 223(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 27% (pale brown oil).
1H-NMR (CDCl3) δ: 2.90-3.00 (2H, m), 3.58 (3H, s), 4.00-4.08 (2H, m), 7.16-7.34 (9H, m), 7.51-7.64 (4H, m).
The title compound was obtained in the same manner as the Example 123(4) using the following starting material.
Starting material: the intermediate 223(3); Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 2.77 (2H, brs), 3.80-3.93 (2H, m), 7.14-7.31 (5H, m), 7.36-7.50 (4H, m), 7.63 (2H, brs), 7.75-7.86 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 126(1) and 3-phenylpropyl bromide; Yield: 57.4% (colorless oil).
1H-NMR (CDCl3) δ: 1.83-1.92 (2H, m), 2.63 (2H, t, J=7.8 Hz), 3.58 (3H, s), 3.81 (2H, t, J=7.5 Hz), 7.05-7.08 (2H, m), 7.10-7.13 (2H, m), 7.18-7.29 (3H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 224(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 34.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.87-1.97 (2H, m), 2.67 (2H, t, J=7.5 Hz), 3.58 (3H, s), 3.88 (2H, t, J=7.5 Hz), 7.12-7.20 (3H, m), 7.24-7.32 (6H, m), 7.56-7.61 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 224(2); Yield: 81.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.70-1.75 (2H, m), 2.49-2.57 (2H, m), 3.72-3.78 (2H, m), 7.11-7.26 (5H, m), 7.40-7.46 (4H, m), 7.62-7.66 (2H, m), 7.77-7.80 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 126(1) and 4-phenylbutyl bromide; Yield: 77.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.54-1.62 (4H, m), 2.60 (2H, t, J=7.2 Hz), 3.57 (3H, s), 3.77 (2H, t, J=6.9 Hz), 7.02-7.05 (2H, m), 7.10-7.14 (2H, m), 7.18-7.29 (3H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 225(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 68.6% (brown oil).
1H-NMR (CDCl3) δ: 1.58-1.69 (4H, m), 2.58-2.64 (2H, m), 3.57 (3H, s), 3.81-3.86 (2H, m), 7.11-7.20 (3H, m), 7.23-7.32 (6H, m), 7.54-7.61 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 225(2); Yield: 54.9% (flesh-colored solid).
1H-NMR (DMSO-d6) δ: 1.39-1.54 (4H, m), 3.30-3.36 (2H, m), 3.64-3.72 (2H, m), 7.11-7.25 (5H, m), 7.35-7.37 (2H, m), 7.43-7.46 (2H, m), 7.58-7.63 (2H, m), 7.77-7.80 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 4-phenylbutyl bromide; Yield: 63.3% (white solid).
1H-NMR (CDCl3) δ: 0.91-0.98 (3H, m), 1.38-1.48 (4H, m), 1.71-1.85 (6H, m), 2.67 (2H, t, J=7.2 Hz), 3.19-3.24 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.27 (1H, brs), 6.74-6.80 (3H, m), 7.18-7.31 (7H, m), 7.52-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 226(1) and methyl chloroglyoxylate; Yield: 63.6% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.35-1.44 (4H, m), 1.56-1.66 (4H, m), 1.76-1.82 (2H, m), 2.57-2.62 (2H, m), 3.51-3.60 (4H, m), 3.97-4.03 (3H, m), 6.99 (1H, d, J=8.7 Hz), 7.10-7.32 (8H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 226(2); Yield: 76.9% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.9 Hz), 1.27-1.60 (8H, m), 1.67-1.74 (2H, m), 2.49-2.55 (2H, m), 3.30-3.40 (1H, m), 3.88-4.17 (3H, m), 7.08-7.21 (6H, m), 7.41-7.48 (3H, m), 7.59-7.70 (3H, m), 13.77 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.9 Hz), 1.27-1.60 (8H, m), 1.67-1.74 (2H, m), 2.49-2.55 (2H, m), 3.30-4.17 (4H, m), 7.08-7.21 (6H, m), 7.37-7.44 (3H, m), 7.59-7.72 (3H, m), 13.77 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 193(3) and 4-phenylbutyl bromide; Yield: 91.1% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.38-1.45 (2H, m), 1.56-1.75 (6H, m), 2.61 (2H, t, J=7.2 Hz), 3.57 (3H, s), 3.77 (2H, t, J=7.2 Hz), 3.98 (2H, t, J=6.6 Hz), 6.91 (1H, d, J=8.4 Hz), 7.09-7.17 (5H, m), 7.20-7.27 (4H, m), 7.48-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 227(1); Yield: 77.1% (white solid).
1H-NMR (DMSO-d6) δ: 0.87 (3H, t, J=7.2 Hz), 1.32-1.52 (6H, m), 1.60-1.69 (2H, m), 2.51-2.55 (2H, m), 3.63 (2H, t, J=7.2 Hz), 3.98 (2H, t, J=6.3 Hz), 7.02 (1H, d, J=8.7 Hz), 7.10-7.13 (3H, m), 7.18-7.24 (4H, m), 7.40 (2H, d, J=8.1 Hz), 7.59-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 125(3) and 5-phenylpentyl chloride; Yield: 14.6% (yellow oil).
1H-NMR (CDCl3) δ: 1.35-1.39 (2H, m), 1.57-1.62 (4H, m), 2.56-2.61 (2H, m), 3.57 (3H, s), 3.77-3.82 (2H, m), 7.12-7.19 (4H, m), 7.24-7.32 (5H, m), 7.52-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 228(1); Yield: 67.5% (yellowish-white solid).
1H-NMR (DMSO-d6) δ: 1.19-1.25 (2H, m), 1.44-1.54 (6H, m), 3.59-3.67 (2H, m), 7.12-7.26 (5H, m), 7.35-7.38 (2H, m), 7.43-7.46 (2H, m), 7.60-7.64 (2H, m), 7.77-7.80 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 210(1) and 3-phenylpropyl bromide; Yield: 61.3% (colorless oil).
1H-NMR (CDCl3) δ: 0.98 (3H, t, J=7.5 Hz), 1.70-1.83 (2H, m), 1.85-1.96 (2H, m), 2.65 (2H, t, J=8.4 Hz), 3.58 (3H, s), 3.78-3.84 (2H, m), 3.92-3.97 (2H, m), 6.92 (1H, d, J=9.3 Hz), 7.10-7.29 (9H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 229(1); Yield: 58.3% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.90 (3H, t, J=7.2 Hz), 1.52-1.56 (4H, m), 2.50-2.57 (2H, m), 3.52-3.57 (2H, m), 3.58-4.01 (2H, m), 7.01-7.31 (8H, m), 7.35-7.45 (2H, m), 7.59-7.68 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 197(3) and 3-phenylpropyl bromide; Yield: 86.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.82-0.88 (6H, m), 1.56-1.64 (4H, m), 1.90-1.93 (2H, m), 2.63-2.69 (2H, m), 3.57 (3H, s), 3.78-3.83 (2H, m), 4.11-4.15 (1H, m), 6.88-6.92 (1H, m), 7.11-7.27 (9H, m), 7.48-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 230(1); Yield: 60.5% (whitish-pink solid).
1H-NMR (DMSO-d6) δ: 0.79-0.85 (6H, m), 1.49-1.58 (4H, m), 1.65-1.73 (2H, m), 2.49-2.55 (2H, m), 3.60-3.65 (2H, m), 4.22-4.26 (1H, m), 7.00-7.26 (8H, m), 7.37-7.40 (2H, m), 7.58-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 189(2) and 4-phenylbutyl bromide; Yield: 55.4% (colorless oil).
1H-NMR (CDCl3) δ: 0.96-1.01 (3H, m), 1.47-1.57 (4H, m), 1.70-1.84 (4H, m), 2.66-2.71 (2H, m), 3.20-3.22 (2H, m), 4.03 (2H, t, J=6.6 Hz), 4.27 (1H, brs), 6.73-6.80 (3H, m), 7.11-7.30 (7H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 231(1) and methyl chloroglyoxylate; Yield: 89.1% (yellow oil).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.45-1.52 (2H, m), 1.60-1.68 (4H, m), 1.73-1.80 (2H, m), 2.57-2.63 (2H, m), 3.50-3.57 (5H, m), 3.98-4.05 (2H, m), 6.99 (1H, d, J=8.4 Hz), 7.10-7.32 (8H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 231(2); Yield: 73.3% (yellow solid).
1H-NMR (DMSO-d6) δ: 0.92 (3H, t, J=7.5 Hz), 1.40-1.54 (6H, m), 1.62-1.72 (2H, m), 2.46-2.50 (2H, m), 3.66-4.05 (4H, m), 7.06-7.21 (6H, m), 7.40-7.43 (2H, m), 7.48-7.49 (1H, m), 7.56-7.60 (1H, m), 7.66-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 198(4) and 3-phenylpropyl bromide; Yield: 54.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.05 (3H, t, J=7.5 Hz), 1.50-1.89 (4H, m), 2.29-2.58 (3H, m), 3.67 (3H, s), 3.77-3.87 (1H, m), 3.94 (2H, t, J=6.6 Hz), 6.82 (1H, dd, J=2.7, 8.7 Hz), 6.87 (1H, d, J=2.7 Hz), 6.95-7.00 (2H, m), 7.06 (1H, d, J=8.7 Hz), 7.11-7.27 (5H, m), 7.47-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 232(1); Yield: 19.8% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 0.88 (3H, t, J=7.5 Hz), 1.23-1.74 (4H, m), 2.04-2.35 (3H, m), 3.50-3.77 (3H, m), 6.49-6.85 (4H, m), 6.95-7.23 (6H, m), 7.56 (2H, d, J=8.4 Hz).
Minor isomer: 1H-NMR (CDCl3) δ: 0.98 (3H, t, J=7.2 Hz), 1.23-1.74 (4H, m), 2.04-2.35 (3H, m), 3.50-3.77 (3H, m), 6.49-6.85 (4H, m), 6.95-7.23 (8H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 199(2) and 3-phenylpropyl bromide; Yield: 83.3% (colorless oil).
1H-NMR (CDCl3) δ: 0.95-1.01 (6H, m), 1.68-1.77 (4H, m), 1.99-2.04 (2H, m), 2.73-2.78 (2H, m), 3.21-3.24 (2H, m), 4.15-4.19 (1H, m), 4.38 (1H, brs), 6.70-6.79 (3H, m), 7.20-7.31 (7H, m), 7.51-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 233(1) and methyl chloroglyoxylate; Yield: 70.7% (yellow oil).
1H-NMR (CDCl3) δ: 0.90-0.99 (6H, m), 1.66-1.71 (4H, m), 1.86-1.95 (2H, m), 2.61-2.70 (2H, m), 3.43-3.52 (4H, m), 4.10-4.23 (2H, m), 6.95 (1H, d, J=9.0 Hz), 7.10-7.27 (7H, m), 7.33 (1H, d, J=2.4 Hz), 7.46-7.50 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 233(2); Yield: 85.7% (white solid).
1H-NMR (DMSO-d6) δ: 0.84-0.88 (6H, m), 1.50-1.59 (6H, m), 3.15-3.21 (2H, m), 3.61-4.34 (3H, m), 7.06-7.22 (6H, m), 7.33-7.42 (2H, m), 7.48-7.57 (2H, m), 7.66-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 188(3) and 3-phenylpropyl bromide; Yield: 39.3% (colorless oil).
1H-NMR (CDCl3) δ: 1.06 (3H, t, J=7.2 Hz), 1.82-1.92 (2H, m), 1.97-2.02 (2H, m), 2.70-2.78 (2H, m), 3.20-3.26 (2H, m), 3.97-4.01 (2H, m), 4.34 (1H, brs), 6.70-6.80 (3H, m), 7.17-7.32 (7H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 234(1) and methyl chloroglyoxylate; Yield: 90.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=7.2 Hz), 1.78-1.98 (4H, m), 2.62-2.68 (2H, m), 3.53 (3H, s), 3.55-4.02 (4H, m), 6.99 (1H, d, J=8.7 Hz), 7.10-7.28 (7H, m), 7.34 (1H, d, J=2.4 Hz), 7.48-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 234(2); Yield: 79.5% (white solid).
1H-NMR (DMSO-d6) δ: 0.92-0.98 (3H, m), 1.63-1.73 (4H, m), 3.29-3.96 (6H, m), 7.05-7.23 (6H, m), 7.40-7.42 (2H, m), 7.49-7.60 (2H, m), 7.66-7.72 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 189(2) and 3-phenylpropyl bromide; Yield: 85.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.00 (3H, t, J=7.2 Hz), 1.51-1.56 (2H, m), 1.79-1.84 (2H, m), 1.99-2.04 (2H, m), 2.73-2.78 (2H, m), 3.21-3.29 (2H, m), 4.01-4.06 (2H, m), 4.32 (1H, brs), 6.70-6.80 (3H, m), 7.20-7.29 (7H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 235(1) and methyl chloroglyoxylate; Yield: 72.1% (colorless oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.2 Hz), 1.43-1.56 (2H, m), 1.72-1.81 (2H, m), 1.86-1.93 (2H, m), 2.63-2.69 (2H, m), 3.54 (3H, s), 3.57-4.07 (4H, m), 6.99 (1H, d, J=8.7 Hz), 7.10-7.18 (2H, m), 7.21-7.28 (5H, m), 7.34 (1H, d, J=2.4 Hz), 7.48-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 235(2); Yield: 84.7% (white solid).
1H-NMR (DMSO-d6) δ: 0.89-0.94 (3H, m), 1.39-1.41 (2H, m), 1.62-1.69 (4H, m), 3.25-3.35 (2H, m), 3.62-4.61 (4H, m), 7.03-7.21 (6H, m), 7.32-7.72 (6H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 188(3) and 4-phenylbutyl bromide; Yield: 87.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.02-1.07 (3H, m), 1.54-1.86 (6H, m), 2.66-2.70 (2H, m), 3.12-3.18 (2H, m), 3.96-4.00 (2H, m), 4.38 (1H, brs), 6.74-6.80 (2H, m), 7.12-7.28 (8H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 236(1) and methyl chloroglyoxylate; Yield: 73.8% (yellow oil).
1H-NMR (CDCl3) δ: 1.04 (3H, t, J=7.2 Hz), 1.60-1.72 (4H, m), 1.76-1.88 (2H, m), 2.55-2.65 (2H, m), 3.50-3.60 (4H, m), 3.90-4.05 (3H, m), 6.98 (1H, d, J=8.7 Hz), 7.10-7.15 (3H, m), 7.19-7.33 (5H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 236(2); Yield: 88.0% (white solid).
1H-NMR (DMSO-d6) δ: 0.99 (3H, t, J=7.2 Hz), 1.35-1.52 (4H, m), 1.67-1.77 (2H, m), 3.30-4.07 (6H, m), 7.06-7.20 (6H, m), 7.41-7.43 (2H, m), 7.48-7.57 (2H, m), 7.64-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 207(3) and 3-phenylpropyl bromide; Yield: 68.0% (yellow oil).
1H-NMR (CDCl3) δ: 0.97 (6H, t, J=7.5 Hz), 1.65-1.74 (6H, m), 2.33-2.59 (3H, m), 3.67 (3H, s), 3.76-3.82 (1H, m), 4.10-4.17 (1H, m), 6.80 (1H, dd, J=2.7, 8.4 Hz), 6.86 (1H, d, J=2.7 Hz), 6.97-7.00 (2H, m), 7.05 (1H, d, J=8.4 Hz), 7.15-7.25 (5H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 237(1); Yield: 75.8% (white solid).
1H-NMR (DMSO-d6) δ: 0.90 (6H, t, J=7.5 Hz), 1.45-1.64 (6H, m), 2.21-2.45 (3H, m), 3.52-3.62 (1H, m), 4.31-4.35 (1H, m), 6.93-7.05 (4H, m), 7.11-7.22 (4H, m), 7.37-7.44 (2H, m), 7.62-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 208(3) and 3-phenylpropyl bromide; Yield: 68.0% (yellow oil).
1H-NMR (CDCl3) δ: 1.16-1.21 (6H, m), 1.57-1.78 (2H, m), 2.28-2.59 (3H, m), 3.33-3.40 (4H, m), 3.67-3.82 (4H, m), 6.50-6.54 (2H, m), 6.98-7.02 (2H, m), 7.14-7.26 (6H, m), 7.50-7.73 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 238(1); Yield: 71.1% (white solid).
1H-NMR (DMSO-d6) δ: 1.10 (6H, t, J=7.2 Hz), 1.46-1.53 (2H, m), 2.17-2.50 (5H, m), 3.32-3.38 (2H, m), 3.51-3.58 (1H, m), 6.55 (1H, d, J=2.7 Hz), 6.65 (1H, dd, J=2.7, 8.4 Hz), 6.98-7.06 (3H, m), 7.13-7.23 (3H, m), 7.40-7.43 (2H, m), 7.62-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 209(3) and 3-phenylpropyl bromide; Yield: 96.1% (colorless oil).
1H-NMR (CDCl3) δ: 1.35-1.37 (6H, m), 1.56-1.74 (2H, m), 2.30-2.53 (3H, m), 3.67 (3H, s), 3.75-3.86 (1H, m), 4.52-4.60 (1H, m), 6.80 (1H, dd, J=2.7, 8.7 Hz), 6.85 (1H, d, J=2.7 Hz), 6.97-7.00 (2H, m), 7.05 (1H, d, J=8.7 Hz), 7.15-7.26 (5H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 239(1); Yield: 69.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.26-1.40 (8H, m), 2.22-2.41 (4H, m), 4.60-4.68 (1H, m), 6.79-6.87 (2H, m), 6.94-6.97 (2H, m), 7.11-7.16 (4H, m), 7.31-7.34 (2H, m), 7.95-7.98 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 210(1) and 4-phenylbutyl bromide; Yield: 95.7% (yellow oil).
1H-NMR (CDCl3) δ: 0.98 (3H, t, J=7.2 Hz), 1.60-1.78 (6H, m), 2.61 (2H, t, J=6.9 Hz), 3.57 (3H, s), 3.77 (2H, t, J=6.9 Hz), 3.94 (2H, t, J=6.3 Hz), 6.91 (1H, d, J=8.4 Hz), 7.09-7.17 (5H, m), 7.21-7.27 (4H, m), 7.50-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 240(1); Yield: 82.3% (white solid).
1H-NMR (DMSO-d6) δ: 0.92 (3H, t, J=7.2 Hz), 1.36-1.50 (4H, m), 1.62-1.73 (2H, m), 2.49-2.55 (2H, m), 3.60-3.64 (2H, m), 3.93-3.97 (2H, m), 6.99-7.25 (8H, m), 7.39-7.42 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 213(3) and 4-phenylbutyl bromide; Yield: 83.8% (colorless oil).
1H-NMR (CDCl3) δ: 0.85-0.94 (6H, m), 1.56-1.71 (4H, m), 2.59-2.64 (2H, m), 2.87 (4H, q, J=6.9 Hz), 3.53 (3H, s), 3.75-3.79 (2H, m), 6.99-7.04 (3H, m), 7.11-7.17 (3H, m), 7.20-7.26 (4H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 241(1); Yield: 73.0% (white solid).
1H-NMR (DMSO-d6) δ: 0.84 (6H, t, J=6.9 Hz), 1.38-1.50 (4H, m), 2.80 (4H, q, J=6.9 Hz), 3.29-3.33 (2H, m), 3.60-3.64 (2H, m), 7.01-7.22 (8H, m), 7.37-7.39 (2H, m), 7.61-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 5-phenylpentyl chloride; Yield: 20.5% (colorless oil).
1H-NMR (CDCl3) δ: 0.81 (3H, t, J=7.2 Hz), 1.25-1.37 (6H, m), 1.51-1.61 (4H, m), 1.67-1.72 (2H, m), 2.50 (2H, t, J=7.5 Hz), 3.01-3.06 (2H, m), 3.88 (2H, t, J=6.6 Hz), 4.13 (1H, brs), 6.60-6.66 (3H, m), 7.02-7.16 (7H, m), 7.39-7.42 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 242(1) and methyl chloroglyoxylate; Yield: 90.1% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.34-1.46 (6H, m), 1.54-1.64 (4H, m), 1.78-1.84 (2H, m), 2.57 (2H, t, J=7.8 Hz), 3.53-3.55 (4H, m), 3.92-4.04 (3H, m), 6.99 (1H, d, J=8.7 Hz), 7.11-7.17 (3H, m), 7.21-7.28 (4H, m), 7.33 (1H, d, J=2.4 Hz), 7.47-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 242(2); Yield: 90.7% (yellow oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.2 Hz), 1.32-1.43 (6H, m), 1.58-1.63 (4H, m), 1.72-1.80 (2H, m), 2.57 (2H, t, J=7.5 Hz), 3.70-3.79 (2H, m), 3.96 (2H, t, J=6.6 Hz), 6.96 (1H, d, J=8.4 Hz), 7.10-7.17 (3H, m), 7.21-7.27 (4H, m), 7.32 (1H, d, J=2.1 Hz), 7.45-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 216(3) and 4-phenylbutyl bromide; Yield: 47.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.58-1.65 (4H, m), 2.57-2.65 (2H, m), 2.77-2.85 (4H, m), 3.54-3.66 (4H, m), 3.57 (3H, s), 3.74-3.80 (2H, m), 6.97 (1H, d, J=8.7 Hz), 7.04 (1H, d, J=2.4 Hz), 7.08-7.30 (8H, m), 7.58-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 243(1); Yield: 98.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.39-1.59 (4H, m), 2.52-2.58 (2H, m), 2.70-2.80 (4H, m), 3.49-3.59 (4H, m), 3.72 (2H, t, J=6.9 Hz), 7.08-7.26 (8H, m), 7.44-7.48 (2H, m), 7.71-7.76 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and 1-pentanol; Yield: 100.0% (yellow solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.5 Hz), 1.30-1.40 (4H, m), 1.73-1.80 (2H, m), 4.09 (2H, t, J=6.6 Hz), 7.01-7.04 (1H, m), 7.26-7.30 (2H, m), 7.54-7.58 (2H, m), 8.22-8.26 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 244(1); Yield: 98.8% (yellow oil).
1H-NMR (CDCl3) δ: 0.83-0.88 (3H, m), 1.24-1.35 (4H, m), 1.59-1.68 (2H, m), 3.48 (2H, brs), 3.82 (2H, t, J=6.6 Hz), 6.63-6.68 (2H, m), 6.81-6.84 (1H, m), 7.20-7.23 (2H, m), 7.51-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 244(2) and methyl chloroglyoxylate; Yield: 86.3% (white solid).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=7.2 Hz), 1.31-1.34 (4H, m), 1.67-1.74 (2H, m), 3.94-3.97 (5H, m), 6.97 (1H, d, J=9.0 Hz), 7.23-7.29 (2H, m), 7.52 (1H, d, J=2.4 Hz), 7.54-7.57 (2H, m), 7.65 (1H, dd, J=2.4, 9.0 Hz), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 244(3) and 4-phenylbutyl bromide; Yield: 65.4% (colorless oil).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.33-1.39 (4H, m), 1.56-1.76 (6H, m), 2.61 (2H, t, J=6.9 Hz), 3.57 (3H, s), 3.77 (2H, t, J=6.9 Hz), 3.97 (2H, t, J=6.3 Hz), 6.91 (1H, d, J=8.4 Hz), 7.09-7.28 (9H, m), 7.48-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 244(4); Yield: 80.0% (white solid).
1H-NMR (DMSO-d6) δ: 0.83 (3H, t, J=6.6 Hz), 1.24-1.51 (8H, m), 1.63-1.68 (2H, m), 2.49-2.54 (2H, m), 3.60-3.65 (2H, m), 3.95-3.99 (2H, m), 6.99-7.02 (1H, m), 7.09-7.12 (3H, m), 7.18-7.24 (4H, m), 7.38-7.40 (2H, m), 7.58-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-hexanol; Yield: 100.0% (orange solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.31-1.38 (4H, m), 1.40-1.57 (2H, m), 1.83-1.90 (2H, m), 4.15 (2H, t, J=6.3 Hz), 7.15 (1H, d, J=9.0 Hz), 7.28-7.32 (2H, m), 7.55-7.58 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 245(1); Yield: 95.0% (yellow solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.33-1.39 (4H, m), 1.47-1.52 (2H, m), 1.80-1.86 (2H, m), 3.89 (2H, brs), 4.03 (2H, t, J=6.6 Hz), 6.82-6.92 (3H, m), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 245(2) and 4-phenylbutyl bromide; Yield: 26.2% (white solid).
1H-NMR (CDCl3) δ: 0.90-0.92 (3H, m), 1.32-1.86 (12H, m), 2.67 (2H, t, J=7.8 Hz), 3.19-3.26 (2H, m), 4.02 (2H, t, J=6.3 Hz), 4.25-4.31 (1H, m), 6.73-6.80 (3H, m), 7.17-7.30 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 245(3) and methyl chloroglyoxylate; Yield: 100.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=6.9 Hz), 1.32-1.49 (6H, m), 1.60-1.65 (4H, m), 1.73-1.82 (2H, m), 2.58-2.62 (2H, m), 3.51-3.61 (4H, m), 3.97-4.06 (3H, m), 6.90 (1H, d, J=8.7 Hz), 7.10-7.15 (3H, m), 7.19-7.28 (4H, m), 7.32 (1H, d, J=2.4 Hz), 7.46-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 245(4); Yield: 94.8% (flesh-colored solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.89 (3H, m), 1.28-1.52 (10H, m), 1.67-1.75 (2H, m), 2.46-2.52 (2H, m), 3.11-3.62 (2H, m), 3.97-4.02 (2H, m), 7.07-7.20 (6H, m), 7.41-7.43 (2H, m), 7.47-7.52 (2H, m), 7.64-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.89 (3H, m), 1.28-1.52 (10H, m), 1.67-1.75 (2H, m), 2.46-2.52 (2H, m), 3.11-3.62 (2H, m), 3.97-4.02 (2H, m), 7.07-7.20 (6H, m), 7.28-7.29 (2H, m), 7.41-7.57 (2H, m), 7.68-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 215(4) and 4-phenylbutyl bromide; Yield: 69.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.52-1.73 (4H, m), 2.27 (3H, s), 2.47-2.63 (2H, m), 2.54 (6H, s), 3.01-3.02 (1H, m), 3.52 (3H, s), 4.08-4.20 (1H, m), 6.83 (1H, s), 6.88 (1H, s), 7.09-7.27 (7H, m), 7.45-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 246(1); Yield: 74.1% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.40-1.56 (4H, m), 2.21 (3H, s), 2.47 (6H, s), 2.48-2.58 (2H, m), 2.81-2.93 (1H, m), 3.88-3.99 (1H, m), 6.86 (1H, s), 6.87 (1H, s), 7.07-7.23 (5H, m), 7.37-7.43 (2H, m), 7.55-7.60 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.40-1.56 (4H, m), 2.09 (3H, s), 2.48 (6H, s), 2.48-2.58 (2H, m), 3.38-3.52 (1H, m), 3.57-3.70 (1H, m), 6.82 (1H, s), 6.94 (1H, s), 7.07-7.23 (5H, m), 7.37-7.43 (2H, m), 7.60-7.65 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 217(3) and 4-phenylbutyl bromide; Yield: 67.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.41-1.52 (6H, m), 1.56-1.65 (4H, m), 2.61 (2H, t, J=6.9 Hz), 2.73-2.80 (4H, m), 3.56 (3H, s), 3.73-3.79 (2H, m), 6.94-7.27 (10H, m), 7.58-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 247(1); Yield: 80.7% (white solid).
1H-NMR (DMSO-d6) δ: 1.34-1.57 (10H, m), 2.49-2.55 (2H, m), 2.62-2.78 (4H, m), 3.58-3.67 (2H, m), 6.95-7.23 (8H, m), 7.38-7.44 (2H, m), 7.71-7.76 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 211(4) and 4-phenylbutyl bromide; Yield: 51.2% (yellow oil).
1H-NMR (CDCl3) δ: 1.29 (6H, d, J=6.0 Hz), 1.61-1.67 (4H, m), 2.61 (2H, t, J=7.2 Hz), 3.56 (3H, s), 3.77 (2H, t, J=7.2 Hz), 4.49-4.56 (1H, m), 6.92 (1H, d, J=9.0 Hz), 7.07-7.26 (9H, m), 7.49-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 248(1); Yield: 78.9% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (6H, d, J=6.0 Hz), 1.37-1.52 (4H, m), 2.48-2.51 (2H, m), 3.59-3.63 (2H, m), 4.54-4.59 (1H, m), 6.99-7.24 (8H, m), 7.37-7.40 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 218(3) and 4-phenylbutyl bromide; Yield: 74.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.14 (9H, s), 1.59-1.68 (4H, m), 2.62 (2H, t, J=7.2 Hz), 3.53 (3H, s), 3.79 (2H, t, J=6.9 Hz), 7.05-7.27 (10H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 249(1); Yield: 75.0% (white solid).
1H-NMR (DMSO-d6) δ: 1.10 (9H, s), 1.40-1.49 (4H, m), 2.48-2.52 (2H, m), 3.64-3.68 (2H, m), 7.05-7.32 (8H, m), 7.39-7.41 (2H, m), 7.58-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 219(5) and 4-phenylbutyl bromide; Yield: 66.4% (white solid).
1H-NMR (CDCl3) δ: 1.40-1.83 (8H, m), 2.32-2.64 (4H, m), 2.92-2.98 (1H, m), 3.28-3.34 (1H, m), 3.59 (3H, s), 3.78-3.82 (2H, m), 7.12-7.36 (12H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 250(1); Yield: 88.0% (white solid).
1H-NMR (DMSO-d6) δ: 1.37-1.78 (6H, m), 2.12-2.36 (2H, m), 2.48-2.56 (3H, m), 2.86-2.94 (1H, m), 3.30-3.46 (2H, m), 3.76-3.81 (2H, m), 7.09-7.24 (5H, m), 7.31-7.48 (7H, m), 13.98 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 113(3) and ethyl 2-bromoisobutyrate; Yield: 22.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=7.2 Hz), 1.24 (6H, s), 1.32 (9H, s), 3.85 (2H, q, J=7.2 Hz), 6.80 (1H, dd, J=2.4, 7.2 Hz), 6.93-6.97 (2H, m), 7.00-7.04 (2H, m), 7.24-7.25 (2H, m), 7.32-7.36 (2H, m), 7.59-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 251(1); Yield: 86.8% (white solid).
1H-NMR (DMSO-d6) δ: 1.12 (6H, s), 1.29 (9H, s), 6.81 (1H, dd, J=2.1, 7.2 Hz), 6.92-6.96 (2H, m), 7.07-7.16 (2H, m), 7.40-7.44 (4H, m), 7.61-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 132(3) and 1-chlorohexane; Yield: 10.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=6.9 Hz), 1.24-1.33 (6H, m), 1.53-1.60 (2H, m), 3.58 (3H, s), 3.74 (2H, t, J=7.5 Hz), 6.97-7.05 (4H, m), 7.18-7.24 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 252(1); Yield: 100.0% (white solid).
1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=6.6 Hz), 1.19-1.25 (6H, m), 1.32-1.42 (2H, m), 3.61 (2H, t, J=7.2 Hz), 6.96-7.13 (4H, m), 7.28-7.42 (4H, m).
A mixture of 4-bromoaniline (500 mg, 2.907 mmol), cyclohexanone (285 mg, 2.907 mmol), zinc powder (760 mg, 11.627 mmol), acetic acid (2.5 ml) and water (0.25 ml) was stirred at room temperature for 1 hour, then stirred at 60° C. for 4 hours. The reaction mixture was cooled to room temperature, and filtered. The filtrate was adjusted to pH 9 by addition of a 2 N aqueous solution of sodium hydroxide, and extracted with diisopropyl ether. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (229 mg, 31%) as a pale orange solid.
1H-NMR (CDCl3) δ: 1.01-1.46 (5H, m), 1.53-1.84 (3H, m), 1.93-2.12 (2H, m), 3.11-3.28 (1H, m), 3.53 (1H, brs), 6.40-6.52 (2H, m), 7.16-7.26 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 253(1) and methyl chloroglyoxylate; Yield: 85.0% (colorless oil).
1H-NMR (CDCl3) δ: 0.80-2.16 (10H, m), 3.51 (3H, s), 4.38-4.64 (1H, m), 6.99-7.15 (2H, m), 7.45-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 253(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 60.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.82-2.19 (10H, m), 3.50 (3H, s), 4.40-4.70 (1H, m), 7.16-7.40 (4H, m), 7.48-7.70 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 253(3); Yield: 90.8% (white solid).
1H-NMR (CDCl3) δ: 0.66-2.10 (10H, m), 4.10-4.44 (1H, s), 7.04-7.34 (2H, m), 7.38-7.53 (2H, m), 7.53-7.74 (2H, m), 7.74-7.90 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: 4-bromoaniline and 1-iodopentane; Yield: 22.9% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.80-1.04 (3H, m), 1.16-1.73 (6H, m), 3.05 (2H, t, J=7.2 Hz), 3.48-3.78 (1H, m), 6.38-6.54 (2H, m), 7.17-7.30 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 254(1) and methyl chloroglyoxylate; Yield: 51.4% (colorless oil).
1H-NMR (CDCl3) δ: 0.79-0.95 (3H, m), 1.20-1.38 (4H, m), 1.42-1.68 (2H, m), 3.58 (3H, s), 3.74 (2H, t, J=7.2 Hz), 7.04-7.16 (2H, m), 7.47-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 254(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 77.1% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.80-0.96 (3H, m), 1.20-1.42 (4H, m), 1.48-1.68 (2H, m), 3.58 (3H, s), 3.74-3.87 (2H, m), 7.20-7.39 (4H, m), 7.50-7.68 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 254(3); Yield: 83.7% (white solid).
1H-NMR (DMSO-d6) δ: 0.74-0.94 (3H, m), 1.10-1.33 (4H, m), 1.33-1.53 (2H, m), 3.56-3.86 (2H, m), 7.32-7.56 (4H, m), 7.64-7.76 (2H, m), 7.76-7.90 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromoaniline and 1-bromo-2,2-dimethylpropane; Yield: 8.9% (brown solid).
1H-NMR (CDCl3) δ: 0.97 (9H, s), 2.84 (2H, s), 3.64 (1H, brs), 6.40-6.54 (2H, m), 7.14-7.29 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 255(1) and methyl chloroglyoxylate; Yield: 97.1% (brown oil).
1H-NMR (CDCl3) δ: 0.86 (9H, s), 3.58 (3H, s), 3.71 (2H, s), 7.11-7.21 (2H, m), 7.46-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 255(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 42.0% (brown oil).
1H-NMR (CDCl3) δ: 0.90 (9H, s), 3.58 (3H, s), 3.78 (2H, s), 7.24-7.44 (4H, m), 7.53-7.68 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 255(3); Yield: 83.7% (brown solid).
1H-NMR (DMSO-d6) δ: 0.77 (9H, s), 3.69 (2H, s), 7.26-7.57 (4H, m), 7.57-7.74 (2H, m), 7.74-8.04 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: ethyl 2-(4-bromo-2,6-dimethoxyphenoxy)acetate and 4-(trifluoromethoxy)phenylboronic acid; Yield: 92% (orange oil).
1H-NMR (CDCl3) δ: 1.32 (3H, t, J=7.2 Hz), 3.90 (6H, s), 4.28 (2H, q, J=7.2 Hz), 4.67 (2H, s), 6.72 (2H, s), 7.25-7.29 (2H, m), 7.52-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 83(1) using the following starting material.
Starting material: the intermediate 301(1); Yield: 47.2% (white solid).
1H-NMR (CDCl3) δ: 1.33 (3H, t, J=7.2 Hz), 4.32 (2H, q, J=7.2 Hz), 4.65 (2H, s), 6.71 (2H, s), 6.84 (2H, s), 7.23-7.27 (2H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 301(2) and 4-(tert-butyl)benzyl bromide; Yield: 17% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (3H, t, J=6.9 Hz), 1.35 (9H, s), 4.27 (2H, q, J=6.9 Hz), 4.69 (2H, s), 5.11 (2H, s), 6.69 (1H, d, J=1.8 Hz), 6.83 (1H, d, J=1.8 Hz), 7.23-7.31 (2H, m), 7.38-7.53 (6H, m), 8.96 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 301(3) and 1-chloropentane; Yield: 66% (colorless oil).
1H-NMR (CDCl3) δ: 0.86-0.96 (6H, m), 1.23-1.50 (17H, m), 1.60-1.69 (2H, m), 1.78-1.88 (2H, m), 4.03 (2H, t, J=6.6 Hz), 4.15 (2H, t, J=6.9 Hz), 4.67 (2H, s), 5.14 (2H, s), 6.72 (1H, d, J=1.8 Hz), 6.76 (1H, d, J=1.8 Hz), 7.22-7.27 (2H, m), 7.36-7.44 (4H, m), 7.45-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 301(4); Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, d, J=6.9 Hz), 1.23-1.50 (13H, m), 1.84-1.94 (2H, m), 4.08-4.13 (2H, m), 4.66 (2H, s), 5.15 (2H, s), 6.74-6.76 (1H, m), 6.82-6.84 (1H, m), 7.26-7.52 (8H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 12(2); Yield: 96.8% (yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.69 (1H, s), 6.93 (1H, d, J=8.1 Hz), 6.96-7.05 (3H, m), 7.20-7.31 (3H, m), 7.33-7.42 (2H, m), 7.51-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 302(1) and ethyl bromoacetate; Yield: 74.5% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.74 (2H, s), 6.92-6.99 (2H, m), 7.02 (1H, d, J=8.1 Hz), 7.11-7.19 (2H, m), 7.21-7.30 (2H, m), 7.30-7.38 (2H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 302(2); Yield: 86.5% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.34 (2H, s), 6.84-6.92 (2H, m), 6.95 (1H, d, J=8.1 Hz), 7.12 (1H, dd, J=8.1, 2.1 Hz), 7.16 (1H, d, J=2.1 Hz), 7.26-7.35 (2H, m), 7.35-7.44 (2H, m), 7.65-7.75 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 302(1) and ethyl 2-bromohexanoate; Yield: 98.5% (colorless oil).
1H-NMR (CDCl3) δ: 0.82 (3H, t, J=7.2 Hz), 1.15-1.37 (16H, m), 1.74-1.95 (2H, m), 4.17 (2H, q, J=7.2 Hz), 4.68 (1H, dd, J=5.1, 7.5 Hz), 6.88-6.95 (2H, m), 7.04 (1H, d, J=9.0 Hz), 7.11-7.17 (2H, m), 7.23-7.35 (4H, m), 7.49-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 303(1); Yield: 73.4% (white solid).
1H-NMR (DMSO-d6) δ: 0.73 (3H, t, J=6.6 Hz), 1.02-1.38 (13H, m), 1.60-1.79 (2H, m), 4.86 (1H, t, J=6.3 Hz), 6.78-6.92 (2H, m), 7.12 (1H, d, J=8.1, Hz), 7.21 (1H, d, J=2.1 Hz), 7.27 (1H, dd, J=2.1, 8.1 Hz), 7.29-7.38 (2H, m), 7.40-7.50 (2H, m), 7.70-7.81 (2H, m), 13.08 (1H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 75(2); Yield: 75.3% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.11 (2H, s), 5.74 (1H, s), 7.00 (1H, d, J=8.4 Hz), 7.07 (1H, dd, J=2.4, 8.4 Hz), 7.12 (1H, d, J=2.4 Hz), 7.20-7.28 (2H, m), 7.33-7.41 (2H, m), 7.41-7.47 (2H, m), 7.47-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 304(1) and ethyl bromoacetate; Yield: 89.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (3H, t, J=7.2 Hz), 1.33 (9H, s), 4.25 (2H, q, J=7.2 Hz), 4.73 (2H, s), 5.17 (2H, s), 9.95 (1H, d, J=8.4 Hz), 7.08 (1H, dd, J=2.1, 8.4 Hz), 7.13 (1H, d, J=2.1 Hz), 7.20-7.28 (2H, m), 7.41 (4H, s), 7.44-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 304(2); Yield: 66.4% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 4.73 (2H, s), 5.18 (2H, s), 6.96 (1H, d, J=8.7 Hz), 7.19 (1H, dd, J=2.1, 8.7 Hz), 7.33-7.50 (7H, m), 7.70-7.80 (2H, m), 12.99 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 110(2) and ethyl 2-bromohexanoate; Yield: 97.7% (colorless oil).
1H-NMR (CDCl3) δ: 0.81 (3H, t, J=7.2 Hz), 1.18-1.35 (16H, m), 1.72-1.93 (2H, m), 4.18 (2H, q, J=7.2 Hz), 4.58-4.68 (1H, m), 6.86-6.94 (2H, m), 6.98 (1H, d, J=8.1 Hz), 7.18-7.35 (6H, m), 7.45-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 305(1); Yield: 52.8% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.71 (3H, t, J=6.6 Hz), 1.00-1.18 (4H, m), 1.25 (9H, s), 1.60-1.73 (2H, m), 4.68 (1H, t, J=6.0 Hz), 6.79-6.90 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.26-7.35 (2H, m), 7.35-7.46 (3H, m), 7.49 (1H, dd, J=2.7, 8.4 Hz), 7.70-7.81 (2H, m), 13.07 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 115(1) and ethyl 2-bromohexanoate; Yield: 24.2% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.2 Hz), 1.22 (3H, t, J=7.2 Hz), 1.30-1.45 (2H, m), 1.45-1.62 (2H, m), 1.76-2.07 (6H, m), 2.66-2.75 (2H, m), 3.95-4.12 (2H, m), 4.12-4.29 (2H, m), 4.62-4.72 (1H, m), 6.89-6.97 (1H, m), 7.08-7.34 (9H, m), 7.45-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 306(1); Yield: 75.1% (white solid).
1H-NMR (DMSO-d6) δ: 0.84 (3H, t, J=7.2 Hz), 1.20-1.38 (2H, m), 1.38-1.53 (2H, m), 1.65-1.92 (6H, m), 2.65-2.76 (2H, m), 3.88-4.16 (2H, m), 4.77 (1H, t, J=6.0 Hz), 7.07 (1H, d, J=8.4 Hz), 7.12 (1H, d, J=2.4 Hz), 7.13-7.33 (6H, m), 7.37-7.47 (2H, m), 7.64-7.74 (2H, m), 12.94 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and phenol; Yield: 68.8% (-like substance).
1H-NMR (CDCl3) δ: 6.98 (1H, d, J=8.4 Hz), 7.08-7.17 (2H, m), 7.18-7.26 (1H, m), 7.26-7.35 (2H, m), 7.38-7.49 (2H, m), 7.56-7.65 (2H, m), 7.70 (1H, dd, J=2.7, 8.4 Hz), 8.13 (1H, d, J=2.7 Hz), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 307(1); Yield: 66.9% (yellow solid).
1H-NMR (CDCl3) δ: 5.74 (1H, s), 6.92 (1H, d, J=8.4 Hz), 7.02 (1H, dd, J=2.4, 8.4 Hz), 7.04-7.10 (2H, m), 7.10-7.18 (1H, m), 7.22-7.30 (3H, m), 7.30-7.41 (2H, m), 7.51-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 307(2) and ethyl 2-bromohexanoate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.76-0.86 (3H, m), 1.14-1.52 (7H, m), 1.72-1.92 (2H, m), 4.17 (2H, q, J=7.2 Hz), 4.02-4.70 (1H, m), 6.94-7.19 (6H, m), 7.23-7.36 (4H, m), 7.49-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 307(3); Yield: 75.3% (white solid).
1H-NMR (DMSO-d6) δ: 0.73 (3H, t, J=6.9 Hz), 0.99-1.24 (4H, m), 1.60-1.78 (2H, m), 4.79-4.96 (1H, m), 6.86-6.99 (2H, m), 6.99-7.10 (1H, m), 7.16 (1H, d, J=8.1 Hz), 7.21 (1H, d, J=2.1 Hz), 7.25-7.39 (3H, m), 7.40-7.53 (2H, m), 7.71-7.83 (2H, m), 13.05 (1H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 95(4); Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.05 (2H, s), 5.76 (1H, s), 6.50 (1H, dd, J=3.0, 8.7 Hz), 6.66 (1H, d, J=3.0 Hz), 6.90 (1H, d, J=8.7 Hz), 6.94-6.99 (2H, m), 7.11-7.18 (2H, m), 7.33-7.39 (2H, m), 7.41-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 308(1) and ethyl 2-bromohexanoate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=7.2 Hz), 1.17 (3H, t, J=7.2 Hz), 1.31-1.54 (4H, m), 1.33 (9H, s), 1.83-2.02 (2H, m), 4.04-4.19 (2H, m), 4.60 (1H, dd, J=2.7, 4.5 Hz), 5.03 (1H, d, J=11.4 Hz), 5.10 (1H, d, J=11.4 Hz), 6.55-6.63 (2H, m), 6.89-6.96 (3H, m), 7.10-7.17 (2H, m), 7.35-7.43 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 308(2); Yield: 47% (white solid).
1H-NMR (DMSO-d6) δ: 0.82 (3H, t, J=7.2 Hz), 1.17-1.48 (4H, m), 1.26 (9H, s), 1.68-1.82 (2H, m), 4.17 (1H, brs), 4.99 (1H, d, J=11.7 Hz), 5.06 (1H, d, J=11.7 Hz), 6.42 (1H, dd, J=2.4, 8.4 Hz), 6.56 (1H, d, J=2.4 Hz), 6.92-7.00 (3H, m), 7.25-7.33 (2H, m), 7.33-7.43 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 95(3) and 4-phenylbutyl bromide; Yield: 99% (colorless oil).
1H-NMR (CDCl3) δ: 1.77-1.97 (4H, m), 2.71 (2H, t, J=7.2 Hz), 4.09 (2H, t, J=6.0 Hz), 6.90-6.99 (3H, m), 7.12-7.35 (8H, m), 7.47 (1H, d, J=3.3 Hz), 10.46 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 309(1); Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 1.74-1.93 (4H, m), 2.70 (2H, t, J=6.9 Hz), 4.04 (2H, t, J=6.0 Hz), 5.69 (1H, s), 6.49 (1H, dd, J=2.7, 9.0 Hz), 6.65 (1H, d, J=2.7 Hz), 6.78 (1H, d, J=9.0 Hz), 6.91-6.98 (2H, m), 7.11-7.17 (2H, m), 7.17-7.34 (5H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 309(2) and ethyl 2-bromohexanoate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.18 (3H, t, J=7.2 Hz), 1.27-1.42 (2H, m), 1.43-1.54 (2H, m), 1.76-2.01 (6H, m), 2.64-2.77 (2H, m), 3.94-4.07 (2H, m), 4.08-4.22 (2H, m), 4.57 (1H, dd, J=5.1, 6.9 Hz), 6.58-6.63 (2H, m), 6.82-6.87 (1H, m), 6.88-6.95 (2H, m), 7.10-7.16 (2H, m), 7.17-7.32 (5H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 309(3); Yield: 94% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.80 (3H, t, J=7.2 Hz), 1.21-1.45 (4H, m), 1.63-1.86 (6H, m), 2.64 (2H, t, J=7.2 Hz), 3.88-4.06 (2H, m), 4.61 (1H, t, J=6.0 Hz), 6.55-6.61 (2H, m), 6.93-7.02 (3H, m), 7.11-7.36 (7H, m), 12.94 (1H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 18(1) and ethyl 2-bromohexanoate; Yield: 80.2% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.26 (3H, t, J=7.2 Hz), 1.34-1.64 (4H, m), 1.98-2.14 (2H, m), 4.24 (2H, q, J=7.2 Hz), 4.79-4.84 (1H, m), 6.91 (1H, d, J=8.7 Hz), 7.23-7.36 (2H, m), 7.53-7.64 (2H, m), 7.70 (1H, dd, J=2.4, 8.7 Hz), 8.07 (1H, d, J=2.4 Hz), 10.63 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 310(1); Yield: 74.9% (yellow oil).
1H-NMR (1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.27 (3H, t, J=7.2 Hz), 1.35-1.52 (2H, m), 1.52-1.68 (2H, m), 1.92-2.08 (2H, m), 4.10-4.33 (2H, m), 4.48-4.63 (1H, m), 6.92 (1H, d, J=8.1 Hz), 7.00 (1H, dd, J=2.1, 8.1 Hz), 7.12 (1H, s), 7.17 (1H, d, J=2.1 Hz), 7.20-7.32 (2H, m), 7.48-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 310(2) and 4-(tert-butyl)benzyl bromide; Yield: 44.2% (colorless oil).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.5 Hz), 1.18-1.64 (16H, m), 1.85-2.09 (2H, m), 4.08-4.28 (2H, m), 4.62-4.76 (1H, m), 5.11 (1H, d, J=11.7 Hz), 5.17 (1H, d, J=11.7 Hz), 6.96 (1H, d, J=8.4 Hz), 7.06 (1H, dd, J=2.4, 8.4 Hz), 7.12 (1H, d, J=2.4 Hz), 7.19-7.28 (2H, m), 7.36-7.45 (4H, m), 7.45-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 310(3); Yield: 91.2% (white solid).
1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=7.5 Hz), 1.22-1.51 (13H, m), 1.80-1.92 (2H, m), 4.69 (1H, t, J=6.0 Hz), 5.19 (2H, s), 6.93 (1H, d, J=8.4 Hz), 7.19 (1H, dd, J=2.4, 8.4 Hz), 7.33-7.48 (7H, m), 7.68-7.79 (2H, m), 13.00 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 310(2) and 4-phenylbutyl bromide; Yield: 20.6% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.2 Hz), 1.23 (3H, t, J=7.2 Hz), 1.29-2.08 (9H, m), 2.58 (1H, t, J=7.2 Hz), 2.63-2.77 (2H, m), 3.92-4.32 (4H, m), 4.58-4.73 (1H, m), 6.87-7.38 (10H, m), 7.44-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 311(1); Yield: 56.3% (white solid).
1H-NMR (DMSO-d6) δ: 0.84 (3H, t, J=7.5 Hz), 1.20-1.38 (2H, m), 1.38-1.52 (2H, m), 1.69-1.92 (6H, m), 2.61-2.73 (2H, m), 4.00-4.22 (2H, m), 4.64 (1H, t, J=6.0 Hz), 6.89 (1H, d, J=8.7 Hz), 7.10-7.34 (7H, m), 7.41 (2H, d, J=9.0 Hz), 7.69-7.80 (2H, m), 12.95 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 99(1); Yield: 82% (pale yellow solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.68 (1H, s), 6.47-6.54 (1H, m), 6.71-6.76 (1H, m), 6.82-6.92 (1H, m), 6.90-7.04 (4H, m), 7.14-7.21 (2H, m), 7.32-7.43 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.72 (1H, s), 6.47-6.54 (1H, m), 6.71-6.76 (1H, m), 6.82-6.92 (1H, m), 6.90-7.04 (4H, m), 7.14-7.21 (2H, m), 7.32-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 312(1) and ethyl 2-bromohexanoate; Yield: 100% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 0.74-0.96 (6H, m), 1.12-1.33 (4H, m), 1.30 (9H, s), 1.65-2.13 (2H, m), 4.02-4.28 (2H, m), 4.48-4.57 (1H, m), 6.58-6.64 (2H, m), 6.84-6.95 (3H, m), 6.96-7.03 (2H, m), 7.13-7.21 (2H, m), 7.25-7.36 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.74-0.96 (6H, m), 1.12-1.33 (4H, m), 1.31 (9H, s), 1.65-2.13 (2H, m), 4.02-4.28 (2H, m), 4.48-4.57 (1H, m), 6.58-6.64 (2H, m), 6.84-6.95 (3H, m), 6.96-7.03 (2H, m), 7.13-7.21 (2H, m), 7.25-7.36 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 312(2); Yield: 84% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 0.81 (3H, t, J=6.9 Hz), 1.18-1.37 (4H, m), 1.30 (9H, s), 1.82-1.94 (2H, m), 4.61 (1H, q, J=6.0 Hz), 6.60-6.73 (2H, m), 6.85-7.08 (5H, m), 7.14-7.22 (2H, m), 7.29-7.37 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.81 (3H, t, J=6.9 Hz), 1.18-1.37 (4H, m), 1.32 (9H, s), 1.82-1.94 (2H, m), 4.61 (1H, q, J=6.0 Hz), 6.60-6.73 (2H, m), 6.85-7.08 (5H, m), 7.14-7.22 (2H, m), 7.29-7.37 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 105(1) and ethyl 2-bromohexanoate; Yield: 60.2% (white solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=7.5 Hz), 1.14-1.64 (16H, m), 1.84-2.09 (2H, m), 4.05-4.26 (2H, m), 4.70 (1H, dd, J=5.1, 7.5 Hz), 5.12 (2H, dd, J=11.7, 16.8 Hz), 7.01 (1H, d, J=8.4 Hz), 7.10-7.19 (2H, m), 7.20-7.28 (2H, m), 7.36-7.45 (4H, m), 7.46-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 313(1); Yield: 72.9% (white solid).
1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=7.2 Hz), 1.18-1.56 (13H, m), 1.78-1.94 (2H, m), 4.84 (1H, t, J=6.3 Hz), 5.12 (1H, d, J=12.3 Hz), 5.16 (1H, d, J=12.3 Hz), 7.12-7.19 (2H, m), 7.23 (1H, dd, J=1.8, 8.7 Hz), 7.37-7.49 (6H, m), 7.65-7.73 (2H, m), 12.95 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 5-bromo-2-fluorobenzaldehyde and 4-(tert-butyl)phenol; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.79 (1H, d, J=8.7 Hz), 6.96-7.03 (2H, m), 7.38-7.44 (2H, m), 7.56 (1H, dd, J=2.4, 8.7 Hz), 8.02 (1H, d, J=2.4 Hz), 10.45 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 314(1); Yield: 82% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 5.67 (1H, s), 6.72 (1H, d, J=8.7 Hz), 6.90-6.98 (3H, m), 7.19 (1H, d, J=2.4 Hz), 7.32-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 314(2) and ethyl bromoacetate; Yield: quantitative (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=6.9 Hz), 1.31 (9H, s), 4.22 (2H, q, J=6.9 Hz), 4.66 (2H, s), 6.83 (1H, d, J=9.0 Hz), 6.86-6.93 (2H, m), 7.05-7.11 (2H, m), 7.28-7.25 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 314(3) and 3-(trifluoromethyl)phenylboronic acid; Yield: 83% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.76 (2H, s), 6.92-7.10 (3H, m), 7.16-7.22 (2H, m), 7.30-7.39 (2H, m), 7.50-7.63 (2H, m), 7.68-7.74 (1H, m), 7.75-7.79 (1H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 314(4); Yield: 87% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.77 (2H, s), 6.94-7.00 (2H, m), 7.03-7.10 (1H, m), 7.20-7.27 (2H, m), 7.34-7.40 (2H, m), 7.52-7.64 (2H, m), 7.68-7.74 (1H, m), 7.75-7.80 (1H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 79(1); Yield: 95.5% (yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.60 (1H, s), 6.91-6.99 (4H, m), 7.12 (1H, dd, J=2.4, 8.6 Hz), 7.36-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 315(1) and ethyl 2-bromoacetate; Yield: 95.2% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.1 Hz), 1.32 (9H, s), 4.22 (2H, q, J=7.1 Hz), 4.67 (2H, s), 6.85 (1H, d, J=8.6 Hz), 6.91-6.95 (2H, m), 7.05 (1H, d, J=2.4 Hz), 7.16 (1H, dd, J=2.4, 8.6 Hz), 7.32-7.37 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 3-(trifluoromethyl)phenylboronic acid; Yield: 48.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 1.31 (9H, s), 4.24 (2H, q, J=7.1 Hz), 4.73 (2H, s), 6.93-6.98 (2H, m), 7.05 (1H, d, J=8.4 Hz), 7.24 (1H, d, J=2.2 Hz), 7.30-7.34 (3H, m), 7.43-7.57 (2H, m), 7.63-7.67 (1H, m), 7.72 (1H, brs).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 315(3); Yield: 81.2% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.73 (2H, s), 6.93-6.98 (2H, m), 7.10 (1H, d, J=8.6 Hz), 7.26 (1H, d, J=2.0 Hz), 7.33-7.38 (3H, m), 7.48-7.59 (2H, m), 7.64-7.67 (1H, m), 7.72 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 314(3) and 3-methylphenylboronic acid; Yield: 60% (colorless oil).
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.2 Hz), 1.31 (9H, s), 2.42 (3H, s), 4.22 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.91-7.05 (3H, m), 7.13-7.21 (3H, m), 7.29-7.37 (5H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 316(1); Yield: 70% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.42 (3H, s), 4.75 (2H, s), 6.91-7.06 (3H, m), 7.15-7.28 (4H, m), 7.30-7.38 (4H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 314(2) and ethyl 2-bromohexanoate; Yield: quantitative (colorless oil).
1H-NMR (CDCl3) δ: 0.74-0.85 (3H, m), 1.20-1.35 (7H, m), 1.30 (9H, s), 1.71-1.90 (2H, m), 4.13-4.25 (2H, m), 4.57 (1H, dd, J=5.1, 7.2 Hz), 6.83-6.90 (2H, m), 7.00-7.10 (3H, m), 7.26-7.32 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 317(1) and 3-methylphenylboronic acid; Yield: 72% (colorless oil).
1H-NMR (CDCl3) δ: 0.81 (3H, t, J=6.9 Hz), 1.21 (3H, t, J=6.9 Hz), 1.22-1.36 (4H, m), 1.36 (9H, s), 1.75-1.90 (2H, m), 2.41 (3H, s), 4.11-4.23 (2H, m), 4.67 (1H, dd, J=5.4, 7.2 Hz), 6.88-6.95 (2H, m), 7.01-7.06 (1H, m), 7.11-7.21 (3H, m), 7.26-7.36 (5H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 317(2); Yield: 58% (colorless oil).
1H-NMR (CDCl3) δ: 0.85 (3H, t, J=6.9 Hz), 1.22-1.47 (4H, m), 1.31 (9H, s), 1.89-1.98 (2H, m), 2.41 (3H, s), 4.76 (1H, t, J=6.0 Hz), 6.90-6.97 (2H, m), 7.01-7.05 (1H, m), 7.12-7.24 (3H, m), 7.28-7.36 (5H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 317(1) and 3-(trifluoromethyl)phenylboronic acid; Yield: 76% (colorless oil).
1H-NMR (CDCl3) δ: 0.82 (3H, t, J=6.9 Hz), 1.22 (3H, t, J=6.9 Hz), 1.22-1.36 (4H, m), 1.31 (9H, s), 1.76-1.92 (2H, m), 4.12-4.23 (2H, m), 4.67 (1H, dd, J=5.4, 7.2 Hz), 6.88-6.96 (2H, m), 7.02-7.09 (1H, m), 7.12-7.22 (2H, m), 7.28-7.35 (2H, m), 7.48-7.63 (2H, m), 7.76-7.79 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 318(1); Yield: 96% (colorless oil).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=6.9 Hz), 1.20-1.50 (4H, m), 1.32 (9H, s), 1.90-2.01 (2H, m), 4.79 (1H, t, J=6.0 Hz), 6.88-6.96 (2H, m), 7.02-7.09 (1H, m), 7.12-7.22 (2H, m), 7.28-7.35 (2H, m), 7.48-7.63 (2H, m), 7.76-7.79 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 3-methylphenylboronic acid; Yield: 77.8% (colorless oil).
1H-NMR (CDCl3) δ: 1.28 (3H, t, J=7.1 Hz), 1.32 (9H, s), 2.39 (3H, s), 4.24 (2H, q, J=7.1 Hz), 4.72 (2H, s), 6.94-6.99 (2H, m), 7.03 (1H, d, J=8.6 Hz), 7.11-7.16 (1H, m), 7.25 (1H, d, J=2.2 Hz), 7.27-7.34 (6H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 319(1); Yield: 81.2% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.41 (3H, s), 4.72 (2H, s), 6.95-7.00 (2H, m), 7.09 (1H, d, J=8.4 Hz), 7.14-7.18 (1H, m), 7.25 (1H, d, J=2.2 Hz), 7.27-7.38 (6H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 315(1) and ethyl 2-bromohexanoate; Yield: 94.1% (colorless oil).
1H-NMR (CDCl3) δ: 0.82 (3H, t, J=7.3 Hz), 1.22 (3H, t, J=7.1 Hz), 1.20-1.26 (4H, m), 1.31 (9H, s), 1.78-1.84 (2H, m), 4.17 (2H, q, J=7.1 Hz), 4.57 (1H, dd, J=5.1, 7.1 Hz), 6.81 (1H, d, J=8.6 Hz), 6.87-6.92 (2H, m), 7.09 (1H, d, J=2.4 Hz), 7.14 (1H, dd, J=2.6, 8.6 Hz), 7.28-7.35 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 320(1) and 3-(trifluoromethyl)phenylboronic acid; Yield: 48.8% (colorless oil).
1H-NMR (CDCl3) δ: 0.81 (3H, t, J=7.3 Hz), 1.24-1.34 (4H, m), 1.24 (3H, t, J=7.1 Hz), 1.30 (9H, s), 1.78-1.88 (2H, m), 4.19 (2H, q, J=7.1 Hz), 4.64 (1H, dd, J=5.1, 7.3 Hz), 6.89-6.94 (2H, m), 7.00 (1H, d, J=8.2 Hz), 7.25-7.33 (4H, m), 7.48-7.57 (2H, m), 7.65-7.68 (1H, m), 7.76 (1H, brs).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 320(2); Yield: 87.7% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=7.1 Hz), 1.25-1.34 (4H, m), 1.24 (3H, t, J=7.1 Hz), 1.31 (9H, s), 1.92-1.99 (2H, m), 4.74 (1H, t, J=5.7 Hz), 6.92-6.98 (2H, m), 7.10 (1H, d, J=8.4 Hz), 7.25 (1H, d, J=2.2 Hz), 7.31-7.38 (3H, m), 7.48-7.59 (2H, m), 7.64-7.66 (1H, m), 7.72 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 320(1) and 3-methylphenylboronic acid; Yield: 85.7% (colorless oil).
1H-NMR (CDCl3) δ: 0.80 (3H, t, J=7.1 Hz), 1.20-1.31 (4H, m), 1.23 (3H, t, J=7.1 Hz), 1.30 (9H, s), 1.78-1.88 (2H, m), 2.38 (3H, s), 4.18 (2H, q, J=7.1 Hz), 4.62 (1H, dd, J=4.9, 7.3 Hz), 6.88-6.93 (2H, m), 6.98 (1H, d, J=8.6 Hz), 7.08-7.13 (1H, m), 7.31-7.26 (7H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 321(1); Yield: 63.6% (colorless solid).
1H-NMR (CDCl3) δ: 0.87 (3H, t, J=7.1 Hz), 1.26-1.46 (4H, m), 1.30 (9H, s), 1.92-1.99 (2H, m), 2.38 (3H, s), 4.71 (1H, t, J=5.7 Hz), 6.92-6.97 (2H, m), 7.07 (1H, d, J=8.4 Hz), 7.12-7.16 (1H, m), 7.23-7.36 (7H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 307(2) and ethyl 2-bromooctanoate; Yield: 89% (colorless syrup).
1H-NMR (CDCl3) δ: 0.85 (3H, t, J=6.7 Hz), 1.10-1.34 (11H, m), 1.75-1.87 (2H, m), 4.17 (2H, q, J=7.1 Hz), 4.66 (1H, dd, J=5.3, 7.1 Hz), 6.94-7.17 (6H, m), 7.23-7.34 (4H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 322(1); Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 0.84 (3H, t, J=6.8 Hz), 1.15-1.31 (6H, m), 1.31-1.43 (2H, m), 1.90 (2H, dd, J=6.0, 15.3 Hz), 4.74 (1H, t, J=6.0 Hz), 6.98 (2H, d, J=8.6 Hz), 7.07 (2H, t, J=9.2 Hz), 7.17-7.21 (2H, m), 7.24-7.34 (4H, m), 7.52 (2H, d, J=8.2 Hz).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 302(1) and ethyl 2-bromooctanoate; Yield: 91% (colorless syrup).
1H-NMR (CDCl3) δ: 0.84 (3H, t, J=6.8 Hz), 1.16-1.38 (8H, m), 1.20 (3H, t, J=7.2 Hz), 1.31 (9H, s), 1.74-1.93 (2H, m), 4.17 (2H, q, J=7.1 Hz), 4.68 (1H, dd, J=5.1, 7.3 Hz), 6.92 (2H, d, J=8.8 Hz), 7.04 (1H, d, J=9.0 Hz), 7.12-7.16 (2H, m), 7.24-7.34 (4H, m), 7.53 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 323(1); Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 0.85 (3H, t, J=6.7 Hz), 1.17-1.34 (6H, m), 1.31 (9H, s), 1.35-1.48 (2H, m), 1.88-1.97 (2H, m), 4.76 (1H, t, J=5.9 Hz), 6.94 (2H, d, J=8.8 Hz), 7.03 (1H, d, J=7.9 Hz), 7.15-7.20 (2H, m), 7.24-7.29 (2H, m), 7.34 (2H, d, J=8.8 Hz), 7.52 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-(4-fluorophenyl)butyl bromide; Yield: 87% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.78-1.98 (4H, m), 2.70 (2H, t, J=7.2 Hz), 4.14 (2H, t, J=6.0 Hz), 6.94-7.07 (3H, m), 7.11-7.20 (2H, m), 7.21-7.33 (2H, m), 7.54-7.64 (2H, m), 7.73 (1H, dd, J=2.4, 9.0 Hz), 8.04 (1H, d, J=2.4 Hz), 10.52-10.55 (1H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 324(1); Yield: 39% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.72-1.94 (4H, m), 2.70 (2H, t, J=7.2 Hz), 4.09 (2H, t, J=6.0 Hz), 5.66 (1H, s), 6.89 (1H, d, J=8.1 Hz), 6.94-7.06 (3H, m), 7.11-7.20 (3H, m), 7.21-7.33 (2H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 324(2) and ethyl 2-bromohexanoate; Yield: 49% (colorless oil).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.2 Hz), 1.23 (3H, t, J=7.2 Hz), 1.28-1.64 (4H, m), 1.74-2.03 (6H, m), 2.68 (2H, t, J=7.2 Hz), 3.87-4.10 (2H, m), 4.14-4.24 (2H, m), 4.63-4.70 (1H, m), 6.90-7.02 (3H, m), 7.10-7.28 (6H, m), 7.46-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 324(3); Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.35-1.48 (2H, m), 1.52-1.68 (2H, m), 1.73-1.92 (4H, m), 2.00-2.10 (2H, m), 2.62 (2H, t, J=7.2 Hz), 4.09 (2H, t, J=6.3 Hz), 4.61 (1H, dd, J=5.4, 6.3 Hz), 6.92-7.03 (3H, m), 7.12-7.19 (3H, m), 7.21-7.30 (3H, m), 7.46-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 4-(4-chlorophenyl)butyl bromide; Yield: 67% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.77-1.97 (4H, m), 2.69 (2H, t, J=7.2 Hz), 4.13 (2H, t, J=6.0 Hz), 7.04 (1H, d, J=9.0 Hz), 7.10-7.15 (2H, m), 7.23-7.31 (4H, m), 7.54-7.62 (2H, m), 7.73 (1H, dd, J=2.4, 9.0 Hz), 8.04 (1H, d, J=2.4 Hz), 10.53 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 325(1); Yield: 45% (colorless oil).
1H-NMR (CDCl3) δ: 1.70-1.94 (4H, m), 2.68 (2H, t, J=7.2 Hz), 4.09 (2H, t, J=6.0 Hz), 5.66 (1H, s), 6.89 (1H, d, J=8.1 Hz), 6.94-7.18 (4H, m), 7.21-7.30 (4H, m), 7.50-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 325(2) and ethyl 2-bromohexanoate; Yield: 45% (colorless oil).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.2 Hz), 1.15-1.66 (7H, m), 1.77-2.02 (6H, m), 2.68 (2H, t, J=7.2 Hz), 4.00-4.10 (2H, m), 4.14-4.24 (2H, m), 4.63-4.70 (1H, m), 6.93 (1H, d, J=8.4 Hz), 7.11-7.19 (4H, m), 7.21-7.29 (4H, m), 7.46-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 325(3); Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.34-1.49 (2H, m), 1.53-1.66 (2H, m), 1.72-1.96 (4H, m), 2.00-2.11 (2H, m), 2.68 (2H, t, J=7.2 Hz), 4.08 (2H, t, J=6.0 Hz), 4.61 (1H, t, J=6.3 Hz), 6.97 (1H, d, J=8.4 Hz), 7.11-7.19 (3H, m), 7.21-7.30 (5H, m), 7.46-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and 4-(trifluoromethoxy)phenol; Yield: 75% (pale brown oil).
1H-NMR (CDCl3) δ: 7.00 (1H, d, J=8.6 Hz), 7.14 (2H, d, J=9.2 Hz), 7.25-7.33 (4H, m), 7.60 (2H, d, J=8.8 Hz), 7.73 (1H, dd, J=2.6, 8.6 Hz), 8.15 (1H, d, J=2.4 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 326(1); Yield: 64% (pale yellow syrup).
1H-NMR (CDCl3) δ: 5.60 (1H, s), 6.94 (1H, d, J=8.4 Hz), 7.02-7.11 (3H, m), 7.20-7.30 (5H, m), 7.56 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 326(2) and ethyl 2-bromooctanoate; Yield: 93% (colorless syrup).
1H-NMR (CDCl3) δ: 0.85 (3H, t, J=6.8 Hz), 1.13-1.29 (11H, m), 1.75-1.85 (2H, m), 4.17 (2H, q, J=7.1 Hz), 4.65 (1H, t, J=6.1 Hz), 6.97 (2H, d, J=9.0 Hz), 7.06-7.19 (5H, m), 7.25-7.31 (2H, m), 7.53 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 326(3); Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 0.84 (3H, t, J=6.7 Hz), 1.13-1.38 (8H, m), 1.83-1.92 (2H, m), 4.72 (1H, t, J=6.0 Hz), 6.98 (2H, d, J=9.2 Hz), 7.07-7.29 (7H, m), 7.52 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and 4-(trifluoromethyl)phenol; Yield: 51% (colorless syrup).
1H-NMR (CDCl3) δ: 7.07 (1H, d, J=8.6 Hz), 7.19 (2H, d, J=8.4 Hz), 7.32 (2H, d, J=7.9 Hz), 7.62 (2H, d, J=8.8 Hz), 7.68 (2H, d, J=8.6 Hz), 7.77 (1H, dd, J=2.4, 8.6 Hz), 8.17 (1H, d, J=2.4 Hz), 10.48 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 327(1); Yield: 82% (pale yellow syrup).
1H-NMR (CDCl3) δ: 5.54 (1H, s), 7.00 (1H, d, J=8.4 Hz), 7.09 (1H, dd, J=2.2, 7.9 Hz), 7.14 (2H, d, J=9.0 Hz), 7.25-7.31 (3H, m), 7.58 (2H, d, J=8.4 Hz), 7.62 (2H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 327(2) and ethyl 2-bromooctanoate; Yield: 91% (colorless syrup).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=6.9 Hz), 1.09-1.24 (11H, m), 1.72-1.82 (2H, m), 4.18 (2H, q, J=7.1 Hz), 4.63 (1H, t, J=6.0 Hz), 7.00-7.07 (3H, m), 7.17-7.19 (2H, m), 7.29 (2H, d, J=8.8 Hz), 7.52-7.58 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 327(3); Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=6.8 Hz), 1.08-1.27 (8H, m), 1.79-1.87 (2H, m), 4.70 (1H, t, J=5.9 Hz), 7.02 (2H, d, J=9.0 Hz), 7.10-7.30 (5H, m), 7.51-7.57 (4H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 314(3) and 4-(trifluoromethyl)phenylboronic acid; Yield: 69% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.75 (2H, s), 6.93-7.00 (2H, m), 7.03 (1H, d, J=8.1 Hz), 7.16-7.24 (2H, m), 7.32-7.38 (2H, m), 7.60-7.71 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 328(1); Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.77 (2H, s), 6.93-7.01 (2H, m), 7.05 (1H, d, J=8.7 Hz), 7.21-7.26 (2H, m), 7.33-7.40 (2H, m), 7.61-7.72 (4H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 314(3) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.75 (2H, s), 6.93-7.00 (2H, m), 7.00-7.05 (1H, m), 7.12-7.23 (3H, m), 7.30-7.39 (3H, m), 7.42-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 329(1); Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.76 (2H, s), 6.93-7.00 (2H, m), 7.00-7.05 (1H, m), 7.12-7.23 (3H, m), 7.30-7.39 (3H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(trifluoromethyl)phenylboronic acid; Yield: 64.7% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 1.31 (9H, s), 4.24 (2H, q, J=7.1 Hz), 4.73 (2H, s), 6.93-6.98 (2H, m), 7.04 (1H, d, J=8.4 Hz), 7.24 (1H, d, J=2.2 Hz), 7.30-7.34 (3H, m), 7.56-7.65 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 330(1); Yield: 80.9% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.74 (2H, s), 6.93-6.98 (2H, m), 7.09 (1H, d, J=8.4 Hz), 7.25 (1H, d, J=2.2 Hz), 7.31-7.37 (3H, m), 7.56-7.66 (4H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 75.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.1 Hz), 1.30 (9H, s), 4.23 (2H, q, J=7.1 Hz), 4.72 (2H, s), 6.92-6.97 (2H, m), 7.03 (1H, d, J=8.4 Hz), 7.13-7.17 (1H, m), 7.21 (1H, d, J=2.2 Hz), 7.27-7.35 (4H, m), 7.39-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 331(1); Yield: 81.2% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.71 (2H, s), 6.93-6.97 (2H, m), 7.09 (1H, d, J=8.4 Hz), 7.15-7.19 (1H, m), 7.23 (1H, d, J=2.0 Hz), 7.30-7.43 (6H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 3-(trifluoromethyl)phenylboronic acid; Yield: 97.7% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.01-7.06 (2H, m), 7.12 (1H, d, J=1.5 Hz), 7.39-7.44 (3H, m), 7.52-7.74 (4H, m), 8.03 (1H, d, J=8.1 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 332(1) and malonic acid; Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 6.70 (1H, d, J=16.2 Hz), 6.88-7.00 (2H, m), 7.36-7.42 (3H, m), 7.64-7.81 (4H, m), 7.92-8.00 (2H, m), 8.04 (1H, d, J=8.1 Hz), 12.5 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 332(2); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.55 (2H, t, J=7.5 Hz), 2.85 (2H, t, J=7.5 Hz), 6.90 (2H, d, J=8.4 Hz), 7.24 (1H, s), 7.38 (2H, d, J=8.4 Hz), 7.46-7.53 (2H, m), 7.63-7.71 (2H, m), 7.88-7.91 (2H, m), 12.5 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-(trifluoromethoxy)phenylboronic acid; Yield: 94.4% (colorless oil).
1H-NMR (CDCl3) δ: 7.32-7.36 (2H, m), 7.44 (1H, d, J=1.7 Hz), 7.46-7.49 (1H, m), 7.61-7.67 (2H, m), 7.96 (1H, dd, J=7.5, 8.1 Hz), 10.40 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-(isopropyl)phenol; Yield: 86.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.28 (6H, d, J=6.9 Hz), 2.95 (1H, sept, J=6.9 Hz), 7.03-7.08 (3H, m), 7.25-7.31 (4H, m), 7.34-7.41 (1H, m), 7.51-7.56 (2H, m), 8.02 (1H, d, J=8.2 Hz), 10.55 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 333(2); Yield: 86.3% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.25 (6H, d, J=6.9 Hz), 2.91 (1H, sept, J=6.9 Hz), 5.65 (1H, s), 6.97-7.03 (2H, m), 7.04 (1H, d, J=2.0 Hz), 7.11 (1H, d, J=8.4 Hz), 7.19-7.25 (5H, m), 7.43-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 333(3) and ethyl 2-bromoacetate; Yield: 90.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.24 (6H, d, J=6.9 Hz), 1.27 (3H, t, J=7.1 Hz), 2.89 (1H, sept, J=6.9 Hz), 4.23 (2H, q, J=7.1 Hz), 4.72 (2H, s), 6.93-6.97 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.14-7.30 (6H, m), 7.45-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 333(4); Yield: 96.3% (white solid).
1H-NMR (CDCl3) δ: 1.24 (6H, d, J=7.0 Hz), 2.90 (1H, sept, J=7.0 Hz), 4.73 (2H, s), 6.93-6.98 (2H, m), 7.08 (1H, d, J=8.4 Hz), 7.18-7.30 (6H, m), 7.46-7.51 (2H, m).
Thionyl chloride (0.280 ml) was added to the intermediate 111(1) (160 mg, 0.384 mmol) at 0° C., and the mixture was stirred for 3 hours. A saturated aqueous solution of sodium hydrogen carbonate was added to the residue obtained by evaporation of the reaction mixture under reduced pressure, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (150 mg, 90%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.74 (2H, s), 6.91-7.02 (2H, m), 7.06 (1H, d, J=1.5 Hz), 7.18-7.40 (5H, m), 7.41-7.52 (2H, m), 7.55 (1H, d, J=7.8 Hz).
Sodium cyanide (36 mg, 0.700 mmol) was added to a mixture of the intermediate 334(1) (150 mg, 0.350 mmol) and N,N-dimethylformamide (10 ml), and the mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (118 mg, 79%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.83 (2H, s), 6.91-6.99 (2H, m), 7.05 (1H, d, J=1.5 Hz), 7.20-7.28 (2H, m), 7.31 (1H, dd, J=1.5, 7.8 Hz), 7.34-7.41 (2H, m), 7.44-7.52 (2H, m), 7.56 (1H, d, J=7.8 Hz).
A 2 N aqueous solution of sodium hydroxide (1.0 ml) was added to a mixture of the intermediate 334(2) (118 mg, 0.277 mmol) and ethanol (2 ml), and the mixture was refluxed for 6 hours. The reaction mixture was cooled to room temperature, adjusted to pH 1 by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (44 mg, 35%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.78 (2H, s), 6.91-6.98 (2H, m), 7.05 (1H, d, J=1.5 Hz), 7.18-7.29 (3H, m), 7.30-7.40 (3H, m), 7.41-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 3-(tert-butyl)phenol; Yield: 95.2% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.87-6.91 (1H, m), 7.07 (1H, d, J=1.7 Hz), 7.19-7.28 (4H, m), 7.32 (1H, d, J=7.9 Hz), 7.35-7.39 (1H, m), 7.49-7.56 (2H, m), 8.02 (1H, d, J=8.1 Hz), 10.56 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 335(1) and malonic acid; Yield: 90.7% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 6.63 (1H, d, J=16.2 Hz), 6.80-6.84 (1H, m), 7.05 (1H, d, J=1.7 Hz), 7.15-7.33 (6H, m), 7.47-7.52 (2H, m), 7.72 (1H, d, J=8.1 Hz), 8.16 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 335; Yield: 84.6% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.75 (2H, t, J=7.7 Hz), 3.05 (2H, t, J=7.7 Hz), 6.73-6.77 (1H, m), 7.04 (1H, d, J=1.8 Hz), 7.09-7.16 (2H, m), 7.20-7.27 (4H, m), 7.35 (1H, d, J=7.9 Hz), 7.45-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-bromo-2-hydroxybenzaldehyde and 4-phenylbutyl bromide; Yield: 75% (white solid).
1H-NMR (CDCl3) δ: 1.76-1.97 (4H, m), 2.66-2.75 (2H, m), 4.02-4.10 (2H, m), 7.11-7.34 (7H, m), 7.68 (1H, d, J=8.1 Hz), 10.41 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 337(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 1.81-1.98 (4H, m), 2.67-2.77 (2H, m), 4.12-4.20 (2H, m), 7.05-7.35 (9H, m), 7.55-7.64 (2H, m), 7.90 (1H, d, J=8.1 Hz), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 337(2); Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 1.77-1.94 (4H, m), 2.67-2.75 (2H, m), 4.07-4.15 (2H, m), 5.64 (1H, s), 6.96-7.01 (2H, m), 7.05 (1H, dd, J=1.8, 8.4 Hz), 7.15-7.34 (7H, m), 7.47-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 337(3) and ethyl bromoacetate; Yield: 89% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (3H, t, J=7.2 Hz). 1.80-1.97 (4H, m), 2.67-2.75 (2H, m), 4.06-4.13 (2H, m), 4.26 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.90-6.97 (1H, m), 7.02-7.09 (2H, m), 7.14-7.33 (7H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 337(4); Yield: 51% (white solid).
1H-NMR (CDCl3) δ: 1.77-1.98 (4H, m), 2.67-2.75 (2H, m), 4.07-4.15 (2H, m), 4.71 (2H, s), 7.10-7.12 (3H, m), 7.14-7.33 (7H, m), 7.47-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and ethylene glycol mono-tert-butyl ether; Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 1.24 (9H, s), 3.79 (2H, t, J=5.4 Hz), 4.27 (2H, t, J=5.4 Hz), 7.23 (1H, d, J=8.4 Hz), 7.27-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.1, 8.4 Hz), 8.03 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 351(1); Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.25 (9H, s), 3.74 (2H, t, J=4.5 Hz), 3.97 (2H, s), 4.14 (2H, t, J=4.5 Hz), 6.88-6.92 (3H, m), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 351(2) and 4-phenylbutyl bromide; Yield: 68% (yellow oil).
1H-NMR (CDCl3) δ: 1.23 (9H, s), 1.67-1.92 (4H, m), 2.64-2.70 (2H, m), 3.14-3.22 (2H, m), 3.72 (2H, t, J=5.4 Hz), 4.09-4.13 (2H, m), 4.40 (1H, s), 6.72-7.32 (10H, m), 7.46-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 351(3) and methyl chloroglyoxylate; Yield: 54% (colorless oil).
1H-NMR (CDCl3) δ: 1.22 (9H, s), 1.53-1.72 (4H, m), 2.54-2.65 (2H, m), 3.51 (3H, s), 3.54-4.18 (6H, m), 7.02-7.31 (9H, m), 7.46-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 351(4); Yield: 47% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.16 (9H, s), 1.29-1.55 (4H, m), 2.41-2.55 (2H, m), 3.60-3.72 (3H, m), 4.05-4.18 (3H, m), 7.04-7.71 (12H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.15 (9H, s), 1.29-1.55 (4H, m), 2.41-2.55 (2H, m), 3.60-3.72 (3H, m), 4.05-4.18 (3H, m), 7.04-7.71 (12H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-heptanol; Yield: 52.0% (yellow solid).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=6.9 Hz), 1.29-1.41 (6H, m), 1.45-1.52 (2H, m), 1.82-1.89 (2H, m), 4.15 (2H, t, J=6.6 Hz), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 352(1); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=6.9 Hz), 1.28-1.50 (8H, m), 1.79-1.88 (2H, m), 3.89 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.21-7.24 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 352(2) and 4-phenylbutyl bromide; Yield: 65.1% (white solid).
1H-NMR (CDCl3) δ: 0.89-0.93 (3H, m), 1.35-1.89 (12H, m), 2.61-2.71 (4H, m), 3.99-4.32 (5H, m), 6.72-6.79 (1H, m), 7.10-7.32 (10H, m), 7.52-7.60 (1H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 352(3) and methyl chloroglyoxylate; Yield: 28.2% (yellow oil).
1H-NMR (CDCl3) δ: 0.88-0.92 (3H, m), 1.25-1.49 (8H, m), 1.57-1.71 (4H, m), 1.77-1.86 (2H, m), 2.57-2.69 (2H, m), 3.48-3.60 (4H, m), 3.98-4.08 (3H, m), 6.99 (1H, d, J=9.0 Hz), 7.08-7.32 (8H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 352(4); Yield: 73.4% (yellow solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=7.2 Hz), 1.21-1.48 (12H, m), 1.67-1.74 (2H, m), 2.49-2.53 (2H, m), 3.31-3.35 (1H, m), 3.97-4.02 (3H, m), 7.06-7.20 (6H, m), 7.40-7.43 (2H, m), 7.49-7.51 (2H, m), 7.64-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.85 (3H, t, J=7.2 Hz), 1.21-1.48 (12H, m), 1.67-1.74 (2H, m), 2.49-2.53 (2H, m), 3.31-3.35 (1H, m), 3.62-3.67 (1H, m), 3.97-4.02 (2H, m), 7.06-7.20 (5H, m), 7.28-7.30 (1H, m), 7.40-7.43 (2H, m), 7.54-7.59 (2H, m), 7.67-7.70 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-octanol; Yield: 89.3% (yellow solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.9 Hz), 1.28-1.41 (8H, m), 1.45-1.52 (2H, m), 1.82-1.89 (2H, m), 4.15 (2H, t, J=6.6 Hz), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 353(1); Yield: 93.2% (gray solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.30-1.37 (10H, m), 1.79-1.88 (2H, m), 3.89 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.21-7.24 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 353(2) and 4-phenylbutyl bromide; Yield: 60.5% (colorless oil).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.9 Hz), 1.23-1.50 (10H, m), 1.74-1.82 (6H, m), 2.66-2.69 (2H, m), 3.18-3.22 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.26 (1H, brs), 6.73-6.78 (3H, m), 7.18-7.31 (7H, m), 7.53-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 353(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.26-1.49 (10H, m), 1.57-1.66 (4H, m), 1.70-1.81 (2H, m), 2.51-2.66 (2H, m), 3.50-3.62 (4H, m), 3.82-4.06 (3H, m), 6.98 (1H, d, J=8.7 Hz), 7.09-7.32 (8H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 353(4); Yield: 79.4% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (14H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.97-4.02 (3H, m), 7.06-7.20 (6H, m), 7.40-7.43 (2H, m), 7.49-7.52 (1H, m), 7.64-7.70 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (14H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.61-3.72 (1H, m), 3.97-4.02 (2H, m), 7.06-7.20 (5H, m), 7.29-7.30 (1H, m), 7.40-7.43 (2H, m), 7.49-7.58 (3H, m), 7.64-7.70 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 4-bromo-2-nitrophenol and 4-(trifluoromethoxy)phenylboronic acid; Yield: 72.4% (yellow solid).
1H-NMR (CDCl3) δ: 7.27 (1H, d, J=9.0 Hz), 7.30-7.34 (2H, m), 7.56-7.61 (2H, m), 7.80 (1H, dd, J=2.4, 9.0 Hz), 8.31 (1H, d, J=2.4 Hz), 10.61 (1H, s).
A mixture of 4-phenylbutyl bromide (277 g, 1.30 mmol), the intermediate 354(1) (299 mg, 1.00 mmol), potassium carbonate (207 mg, 1.50 mmol) and dimethylformamide (6 ml) was stirred at 90° C. for 3 hours under argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1) to give the title compound (395 mg, 92%) as a pale yellow solid.
1H-NMR (CDCl3) δ: 1.85-2.01 (4H, m), 2.68-2.74 (2H, m), 4.15 (2H, t, J=6.6 Hz), 7.12 (1H, d, J=8.7 Hz), 7.17-7.32 (7H, m), 7.54-7.58 (2H, m), 7.69 (1H, dd, J=2.7, 8.7 Hz), 8.03 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 354(2); Yield: 86.2% (yellow solid).
1H-NMR (CDCl3) δ: 1.79-1.90 (4H, m), 2.71 (2H, t, J=7.5 Hz), 3.87 (2H, brs), 4.05 (2H, t, J=6.0 Hz), 6.82 (1H, d, J=8.1 Hz), 6.87-6.92 (2H, m), 7.20-7.32 (7H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 354(3) and 4-phenylbutyl bromide; Yield: 41.2% (white solid).
1H-NMR (CDCl3) δ: 1.70-1.89 (8H, m), 2.65-2.72 (4H, m), 3.17-3.23 (2H, m), 4.04 (2H, t, J=6.0 Hz), 4.23-4.27 (1H, m), 6.73-6.79 (3H, m), 7.16-7.22 (6H, m), 7.25-7.31 (6H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 354(4) and methyl chloroglyoxylate; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 1.56-1.66 (4H, m), 1.79-1.83 (4H, m), 2.56-2.61 (2H, m), 2.68 (2H, t, J=6.9 Hz), 3.50-3.56 (4H, m), 3.97-4.05 (3H, m), 6.96 (1H, d, J=9.0 Hz), 7.08-7.32 (13H, m), 7.46-7.50 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 354(5); Yield: 61.9% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.36-1.51 (4H, m), 1.72-1.79 (4H, m), 2.44-2.56 (2H, m), 2.62-2.68 (2H, m), 3.16-3.23 (2H, m), 4.00-4.08 (2H, m), 7.03-7.27 (11H, m), 7.37-7.40 (2H, m), 7.46-7.50 (2H, m), 7.62-7.66 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.36-1.51 (4H, m), 1.72-1.79 (4H, m), 2.44-2.56 (2H, m), 2.62-2.68 (2H, m), 3.16-3.23 (2H, m), 3.58-3.66 (1H, m), 4.08-4.16 (1H, m), 7.03-7.27 (11H, m), 7.37-7.40 (2H, m), 7.46-7.50 (2H, m), 7.62-7.66 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 3-cyclopentyl-1-propanol; Yield: 100% (orange solid).
1H-NMR (CDCl3) δ: 0.86-1.88 (13H, m), 4.14 (2H, t, J=6.3 Hz), 7.15 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m), 7.54-7.58 (2H, m), 7.70 (1H, dd, J=2.4, 8.7 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 355(1); Yield: 75% (white solid).
1H-NMR (CDCl3) δ: 0.85-1.88 (13H, m), 3.89 (2H, brs), 4.03 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=8.1 Hz), 6.87-6.93 (2H, m), 7.21-7.25 (2H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 355(2) and 4-phenylbutyl bromide; Yield: 100% (brown oil).
1H-NMR (CDCl3) δ: 0.83-1.92 (17H, m), 2.64-2.71 (2H, m), 3.18-3.23 (2H, m), 3.96-4.03 (2H, m), 4.27 (1H, brs), 6.73-7.33 (10H, m), 7.46-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 355(3) and methyl chloroglyoxylate; Yield: 63% (colorless oil).
1H-NMR (CDCl3) δ: 1.05-1.94 (17H, m), 2.57-2.67 (2H, m), 3.53 (3H, s), 3.56-4.05 (4H, m), 6.98 (1H, d, J=8.4 Hz), 7.09-7.33 (8H, m), 7.46-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 355(4); Yield: 36% (white solid).
1H-NMR (DMSO-d6) δ: 1.00-1.86 (17H, m), 2.34-2.61 (2H, m), 3.02-4.15 (4H, m), 7.05-7.30 (6H, m), 7.39-7.45 (2H, m), 7.47-7.58 (2H, m), 7.62-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 3-phenoxypropyl bromide; Yield: 54% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.32-1.49 (4H, m), 1.78-1.88 (2H, m), 2.16 (2H, quint, J=6.0 Hz), 3.40-3.50 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.12 (2H, t, J=5.7 Hz), 4.53 (1H, brs), 6.78-6.81 (3H, m), 6.88-6.98 (3H, m), 7.18-7.31 (4H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 356(1) and methyl chloroglyoxylate; Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.30-1.49 (4H, m), 1.76-1.85 (2H, m), 2.06-2.17 (2H, m), 3.54 (3H, s), 3.79-4.16 (6H, m), 6.81-6.85 (2H, m), 6.88-6.94 (1H, m), 6.98 (1H, t, J=8.7 Hz), 7.19-7.30 (4H, m), 7.37 (1H, t, J=2.7 Hz), 7.42-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 356(2); Yield: 65% (white solid).
1H-NMR (CDCl3) δ: 0.85-0.91 (3H, m), 1.24-1.50 (4H, m), 1.62-1.79 (4H, m), 2.87-2.96 (2H, m), 3.72-4.09 (4H, m), 7.07-7.23 (6H, m), 7.32-7.58 (4H, m), 7.62-7.72 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 3-chloropropyl phenyl sulfide; Yield: 42% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.5 Hz), 1.33-1.50 (4H, m), 1.78-1.88 (2H, m), 1.97-2.07 (2H, m), 3.05 (2H, t, J=7.2 Hz), 3.36 (2H, t, J=6.9 Hz), 4.02 (2H, t, J=6.6 Hz), 4.36 (1H, brs), 6.75-6.81 (3H, m), 7.13-7.36 (7H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 357(1) and methyl chloroglyoxylate; Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.33-1.47 (4H, m), 1.74-1.96 (4H, m), 2.96 (2H, t, J=7.2 Hz), 3.54 (3H, s), 3.72-4.08 (4H, m), 6.98 (1H, d, J=9.0 Hz), 7.09-7.33 (8H, m), 7.46-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 357(2); Yield: 63% (white solid).
1H-NMR (DMSO-d6) δ: 0.81-0.89 (3H, m), 1.23-1.42 (4H, m), 1.65-1.93 (4H, m), 3.75-4.03 (6H, m), 6.80-6.90 (3H, m), 7.07-7.26 (3H, m), 7.38-7.41 (2H, m), 7.48-7.58 (2H, m), 7.63-7.73 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 354(3) and 1-chloropentane; Yield: 24.4% (orange oil).
1H-NMR (CDCl3) δ: 0.88-0.94 (3H, m), 1.33-1.42 (4H, m), 1.65-1.71 (2H, m), 1.83-1.88 (2H, m), 2.71 (2H, t, J=7.2 Hz), 3.17 (2H, t, J=7.2 Hz), 4.05 (2H, t, J=6.0 Hz), 4.12 (2H, t, J=6.6 Hz), 4.24 (1H, brs), 6.75-6.79 (3H, m), 7.19-7.29 (7H, m), 7.54-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 358(1) and methyl chloroglyoxylate; Yield: 100% (orange solid).
1H-NMR (CDCl3) δ: 0.82-0.93 (3H, m), 1.26-1.38 (4H, m), 1.51-1.60 (2H, m), 1.81-1.85 (4H, m), 2.67 (2H, t, J=6.6 Hz), 3.48-3.56 (4H, m), 3.89-4.05 (3H, m), 6.98 (1H, d, J=8.7 Hz), 7.19-7.21 (3H, m), 7.26-7.32 (4H, m), 7.36 (1H, d, J=2.4 Hz), 7.47-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 358(2); Yield: 84.9% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.77-0.93 (3H, m), 1.15-1.40 (6H, m), 1.69-1.71 (4H, m), 2.61-2.65 (2H, m), 3.22-3.30 (2H, m), 4.03-4.08 (2H, m), 7.06-7.33 (6H, m), 7.37-7.41 (2H, m), 7.49-7.51 (2H, m), 7.66-7.69 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.77-0.93 (3H, m), 1.15-1.40 (6H, m), 1.69-1.71 (4H, m), 2.61-2.65 (2H, m), 3.63-3.69 (1H, m), 4.03-4.12 (3H, m), 7.06-7.33 (6H, m), 7.37-7.41 (2H, m), 7.52-7.57 (2H, m), 7.66-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 4-bromo-1-fluoro-2-nitrobenzene and 1-pentanol; Yield: 68.6% (clear brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.35-1.55 (4H, m), 1.79-1.86 (2H, m), 4.08 (2H, t, J=6.3 Hz), 6.96 (1H, d, J=9.0 Hz), 7.60 (1H, dd, J=2.4, 9.0 Hz), 7.95 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 359(1); Yield: 99.5% (brown solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.32-1.45 (4H, m), 1.76-1.81 (2H, m), 3.95 (2H, t, J=6.6 Hz), 4.31 (2H, brs), 6.62 (1H, d, J=8.4 Hz), 6.81 (1H, dd, J=2.4, 8.4 Hz), 6.87 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 359(2) and 4-phenylbutyl bromide; Yield: 58.8% (brown oil).
1H-NMR (CDCl3) δ: 0.90-0.94 (3H, m), 1.38-1.45 (4H, m), 1.68-1.81 (6H, m), 2.67 (2H, t, J=7.2 Hz), 3.10 (2H, t, J=6.0 Hz), 3.93 (2H, t, J=6.6 Hz), 4.19-4.27 (1H, m), 6.56 (1H, d, J=8.4 Hz), 6.64 (1H, d, J=2.1 Hz), 6.70 (1H, dd, J=2.1, 8.4 Hz), 7.16-7.31 (5H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 359(3) and methyl chloroglyoxylate; Yield: 54.5% (white solid).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.35-1.41 (4H, m), 1.55-1.62 (4H, m), 1.71-1.79 (2H, m), 2.58-2.63 (2H, m), 3.51-3.62 (4H, m), 3.86-3.96 (3H, m), 6.79 (1H, d, J=8.7 Hz), 7.11-7.29 (6H, m), 7.40 (1H, dd, J=2.7, 8.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 359(4) and 4-fluorophenylboronic acid; Yield: 85.4% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.35-1.46 (4H, m), 1.58-1.69 (4H, m), 1.75-1.85 (2H, m), 2.57-2.64 (2H, m), 3.50-3.61 (4H, m), 3.97-4.06 (3H, m), 6.96 (1H, d, J=8.4 Hz), 7.08-7.16 (5H, m), 7.18-7.25 (2H, m), 7.30 (1H, d, J=2.4 Hz), 7.40-7.49 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 359(5); Yield: 77.6% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.64-1.70 (2H, m), 2.46-2.53 (2H, m), 3.20-3.28 (2H, m), 3.96-4.01 (2H, m), 7.03-7.26 (8H, m), 7.43-7.60 (4H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.64-1.70 (2H, m), 2.46-2.53 (2H, m), 3.64-3.72 (1H, m), 3.96-4.01 (3H, m), 6.92-6.97 (2H, m), 7.03-7.26 (8H, m), 7.43-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 359(4) and phenylboronic acid; Yield: 60.6% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.35-1.46 (4H, m), 1.58-1.69 (4H, m), 1.75-1.85 (2H, m), 2.57-2.64 (2H, m), 3.50-3.61 (4H, m), 3.97-4.06 (3H, m), 6.98 (1H, d, J=8.4 Hz), 7.10-7.16 (3H, m), 7.18-7.25 (2H, m), 7.33-7.36 (2H, m), 7.40-7.55 (5H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 360(1); Yield: 61.5% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.68-1.74 (2H, m), 2.46-2.53 (2H, m), 3.20-3.28 (2H, m), 3.97-4.04 (2H, m), 7.03-7.20 (6H, m), 7.24-7.35 (2H, m), 7.38-7.55 (5H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.89 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.68-1.74 (2H, m), 2.46-2.53 (2H, m), 3.64-3.72 (1H, m), 3.97-4.04 (3H, m), 6.72-6.78 (2H, m), 7.03-7.20 (6H, m), 7.38-7.55 (5H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 359(4) and 4-chlorophenylboronic acid; Yield: 72.6% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.35-1.46 (4H, m), 1.58-1.69 (4H, m), 1.75-1.82 (2H, m), 2.57-2.64 (2H, m), 3.50-3.61 (4H, m), 3.97-4.06 (3H, m), 6.97 (1H, d, J=8.7 Hz), 7.10-7.27 (6H, m), 7.31 (1H, d, J=2.4 Hz), 7.38-7.43 (3H, m), 7.48 (1H, dd, J=2.4, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate SYN361(1); Yield: 31.0% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.64-1.73 (2H, m), 2.46-2.53 (2H, m), 3.20-3.28 (2H, m), 3.96-4.03 (2H, m), 7.04-7.21 (7H, m), 7.44-7.60 (5H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.24-1.50 (8H, m), 1.64-1.73 (2H, m), 2.46-2.53 (2H, m), 3.64-3.72 (1H, m), 3.96-4.03 (3H, m), 6.74-6.78 (2H, m), 7.04-7.21 (5H, m), 7.44-7.60 (5H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 5-fluoro-2-nitrophenol and 1-chloropentane; Yield: 51.4% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.35-1.53 (4H, m), 1.81-1.90 (2H, m), 4.08 (2H, t, J=6.3 Hz), 6.66-6.78 (2H, m), 7.90-7.95 (1H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: the intermediate 362(1) and 4-(trifluoromethoxy)phenol; Yield: 92.2% (clear pale yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.36-1.48 (4H, m), 1.79-1.88 (2H, m), 4.02 (2H, t, J=6.3 Hz), 6.48 (1H, dd, J=2.4, 9.0 Hz), 6.65 (1H, d, J=2.4 Hz), 7.08-7.12 (2H, m), 7.25-7.29 (2H, m), 7.92 (1H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 362(2); Yield: 100% (red oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.36-1.48 (4H, m), 1.76-1.83 (2H, m), 3.73 (2H, brs), 3.93 (2H, t, J=6.3 Hz), 6.48 (1H, dd, J=2.4, 8.4 Hz), 6.64 (1H, d, J=2.4 Hz), 6.69 (1H, d, J=8.4 Hz), 6.89-6.94 (2H, m), 7.10-7.14 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 362(3) and 4-phenylbutyl bromide; Yield: 74.4% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=6.9 Hz), 1.36-1.48 (4H, m), 1.72-1.83 (6H, m), 2.67-2.72 (2H, m), 3.13-3.20 (2H, m), 3.89-3.96 (2H, m), 4.07 (1H, brs), 6.51-6.55 (3H, m), 6.89-6.94 (2H, m), 7.10-7.29 (7H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 362(4) and methyl chloroglyoxylate; Yield: 77.3% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=6.9 Hz), 1.32-1.46 (4H, m), 1.55-1.64 (4H, m), 1.66-1.76 (2H, m), 2.59-2.64 (2H, m), 3.40-3.61 (4H, m), 3.85-4.00 (3H, m), 6.43 (1H, dd, J=2.4, 9.0 Hz), 6.58 (1H, d, J=2.4 Hz), 7.01-7.04 (3H, m), 7.12-7.28 (7H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 362(5); Yield: 100% (clear pale yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.86 (3H, t, J=6.6 Hz), 1.24-1.52 (8H, m), 1.62-1.70 (2H, m), 2.46-2.53 (2H, m), 3.26-3.38 (2H, m), 3.88-3.92 (2H, m), 6.38-6.53 (1H, m), 6.71-6.79 (1H, m), 7.07-7.26 (8H, m), 7.38-7.41 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.86 (3H, t, J=6.6 Hz), 1.24-1.52 (8H, m), 1.62-1.70 (2H, m), 2.46-2.53 (2H, m), 3.19-3.38 (3H, m), 3.50-3.59 (1H, m), 6.38-6.53 (1H, m), 6.71-6.79 (1H, m), 6.96-7.26 (8H, m), 7.38-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 4-bromo-1-fluoro-2-nitrobenzene and 1-pentanol; Yield: 74.1% (brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.38-1.48 (4H, m), 1.79-1.88 (2H, m), 4.08 (2H, t, J=6.3 Hz), 6.96 (1H, d, J=9.0 Hz), 7.60 (1H, dd, J=2.4, 9.0 Hz), 7.95 (1H, d, J=2.4 Hz).
A mixture of the intermediate 363(1) (1.00 g, 3.47 mmol), 4-(trifluoromethoxy)phenol (803 mg, 4.51 mmol), potassium carbonate (959 mg, 6.94 mmol), copper(II) oxide (690 mg, 8.67 mmol) and pyridine (4 ml) was refluxed for 10 hours. The reaction mixture was cooled to room temperature and filtered through Celite. The filtrate was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (512 mg, 38.5%) as a brown oil.
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.38-1.48 (4H, m), 1.79-1.88 (2H, m), 4.08 (2H, t, J=6.3 Hz), 6.97-7.00 (2H, m), 7.04-7.08 (2H, m), 7.18-7.22 (2H, m), 7.50 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting materials.
Starting materials: the intermediate 363(2); Yield: 95.6% (red oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.9 Hz), 1.40-1.46 (4H, m), 1.76-1.85 (2H, m), 3.86 (2H, brs), 3.97 (2H, t, J=6.3 Hz), 6.35 (1H, dd, J=2.7, 8.7 Hz), 6.42 (1H, d, J=2.7 Hz), 6.72 (1H, d, J=8.7 Hz), 6.92-6.95 (2H, m), 7.11-7.14 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 363(3) and 4-phenylbutyl bromide; Yield: 64.3% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=6.9 Hz), 1.36-1.83 (10H, m), 2.67-2.72 (2H, m), 3.13-3.20 (2H, m), 3.89-3.96 (2H, m), 4.07 (1H, brs), 6.26 (1H, dd, J=2.7, 8.7 Hz), 6.30 (1H, d, J=2.7 Hz), 6.67 (1H, d, J=8.7 Hz), 6.92-6.95 (2H, m), 7.10-7.34 (7H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 363(4) and methyl chloroglyoxylate; Yield: 71.6% (orange oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=6.9 Hz), 1.37-1.46 (4H, m), 1.55-1.64 (4H, m), 1.72-1.78 (2H, m), 2.56-2.61 (2H, m), 3.50-3.59 (4H, m), 3.92-4.00 (3H, m), 6.86-6.92 (3H, m), 7.00 (1H, dd, J=3.0, 9.0 Hz), 7.09-7.18 (5H, m), 7.22-7.27 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 363(5); Yield: 52.9% (yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.05-1.11 (2H, m), 1.24-1.52 (6H, m), 1.62-1.70 (2H, m), 2.86-2.93 (2H, m), 3.52-3.61 (2H, m), 3.95-3.99 (2H, m), 6.93-7.13 (8H, m), 7.18-7.22 (2H, m), 7.28-7.32 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.88 (3H, t, J=6.6 Hz), 1.05-1.11 (2H, m), 1.24-1.52 (6H, m), 1.62-1.70 (2H, m), 2.86-2.93 (2H, m), 3.40-3.99 (4H, m), 6.72-6.78 (1H, m), 6.93-7.13 (7H, m), 7.18-7.22 (2H, m), 7.28-7.32 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-nonanol; Yield: 96.7% (orange solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.26-1.41 (10H, m), 1.45-1.52 (2H, m), 1.82-1.89 (2H, m), 4.14 (2H, t, J=6.6 Hz), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 364(1); Yield: 98.4% (yellow solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.25-1.50 (12H, m), 1.79-1.88 (2H, m), 3.89 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.21-7.24 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 364(2) and 4-phenylbutyl bromide; Yield: 78.5% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.86-0.91 (3H, m), 1.24-1.89 (20H, m), 2.61-2.71 (2H, m), 3.99-4.03 (2H, m), 4.28 (1H, brs), 6.72-6.79 (3H, m), 7.10-7.32 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 364(3) and methyl chloroglyoxylate; Yield: 73.5% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.26-1.49 (12H, m), 1.57-1.66 (4H, m), 1.70-1.81 (2H, m), 2.57-2.63 (2H, m), 3.50-3.59 (4H, m), 3.82-4.06 (3H, m), 6.98 (1H, d, J=8.7 Hz), 7.09-7.15 (3H, m), 7.19-7.29 (4H, m), 7.31 (1H, d, J=2.1 Hz), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 364(4); Yield: 34.7% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (16H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.97-4.02 (3H, m), 7.06-7.20 (6H, m), 7.40-7.43 (2H, m), 7.49-7.52 (1H, m), 7.64-7.70 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (16H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.61-3.72 (1H, m), 3.97-4.02 (2H, m), 7.06-7.20 (5H, m), 7.30 (1H, d, J=2.1 Hz), 7.40-7.43 (2H, m), 7.48-7.51 (2H, m), 7.55 (1H, dd, J=2.1, 8.4 Hz), 7.64-7.70 (1H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-decanol; Yield: 66.2% (orange solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.9 Hz), 1.28-1.41 (12H, m), 1.45-1.52 (2H, m), 1.82-1.89 (2H, m), 4.15 (2H, t, J=6.6 Hz), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 356(1); Yield: 98.1% (yellow solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.25-1.55 (14H, m), 1.79-1.88 (2H, m), 3.89 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.93 (2H, m), 7.21-7.24 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 365(2) and 4-phenylbutyl bromide; Yield: 74.3% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.86-0.91 (3H, m), 1.24-1.89 (22H, m), 2.61-2.71 (2H, m), 3.99-4.03 (2H, m), 4.27 (1H, brs), 6.72-6.79 (3H, m), 7.10-7.32 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 365(3) and methyl chloroglyoxylate; Yield: 84.5% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.26-1.49 (14H, m), 1.57-1.66 (4H, m), 1.70-1.81 (2H, m), 2.57-2.63 (2H, m), 3.50-3.59 (4H, m), 3.82-4.06 (3H, m), 6.98 (1H, d, J=8.7 Hz), 7.09-7.15 (3H, m), 7.19-7.29 (4H, m), 7.31 (1H, d, J=2.1 Hz), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 365(4); Yield: 79.7% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (18H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.97-4.02 (3H, m), 7.06-7.20 (6H, m), 7.40-7.43 (2H, m), 7.49-7.52 (1H, m), 7.64-7.70 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.82-0.85 (3H, m), 1.24-1.49 (18H, m), 1.67-1.74 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.61-3.72 (1H, m), 3.97-4.02 (2H, m), 7.06-7.20 (5H, m), 7.30 (1H, d, J=2.1 Hz), 7.40-7.43 (2H, m), 7.48-7.51 (2H, m), 7.55 (1H, dd, J=2.1, 8.4 Hz), 7.64-7.70 (1H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 1-chloropentane; Yield: 45.5% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.91-0.96 (6H, m), 1.28-1.46 (8H, m), 1.65-1.76 (2H, m), 1.79-1.89 (2H, m), 3.17-3.25 (2H, m), 4.00-4.29 (3H, m), 6.77-6.80 (2H, m), 7.17-7.25 (3H, m), 7.54-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 366(1) and methyl chloroglyoxylate; Yield: 60.3% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.86 (3H, t, J=6.9 Hz), 0.94 (3H, t, J=6.9 Hz), 1.28-1.46 (8H, m), 1.53-1.59 (2H, m), 1.79-1.89 (2H, m), 3.48-3.56 (4H, m), 3.92-4.06 (3H, m), 6.99 (1H, d, J=8.7 Hz), 7.26-7.29 (2H, m), 7.36 (1H, d, J=2.1 Hz), 7.48-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 366(2); Yield: 97.0% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.77-0.81 (3H, m), 0.90 (3H, t, J=6.9 Hz), 1.14-1.20 (6H, m), 1.31-1.42 (4H, m), 2.44-2.50 (2H, m), 3.22-3.26 (2H, m), 3.99-4.03 (2H, m), 7.08 (1H, d, J=8.4 Hz), 7.40-7.43 (2H, m), 7.46-7.56 (2H, m), 7.66-7.69 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.77-0.81 (3H, m), 0.90 (3H, t, J=6.9 Hz), 1.14-1.20 (6H, m), 1.31-1.42 (4H, m), 2.44-2.50 (2H, m), 3.53-3.57 (1H, m), 3.99-4.03 (3H, m), 7.14 (1H, d, J=8.4 Hz), 7.30 (1H, d, J=2.7 Hz), 7.40-7.43 (2H, m), 7.46-7.56 (1H, m), 7.66-7.72 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 4-bromo-2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99.2% (orange solid).
1H-NMR (CDCl3) δ: 7.34-7.37 (2H, m), 7.45-7.50 (2H, m), 7.61-7.65 (2H, m), 8.14-8.20 (1H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-pentanol; Yield: 97.4% (yellow solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.39-1.51 (4H, m), 1.82-1.92 (2H, m), 4.17 (2H, t, J=6.6 Hz), 7.16 (1H, dd, J=1.8, 8.4 Hz), 7.19 (1H, d, J=1.8 Hz), 7.31-7.35 (2H, m), 7.58-7.62 (2H, m), 7.93 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 367(2); Yield: 94.9% (yellow solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.37-1.51 (4H, m), 1.82-1.89 (2H, m), 3.89 (2H, brs), 4.06 (2H, t, J=6.6 Hz), 6.77 (1H, d, J=8.1 Hz), 6.97-7.01 (2H, m), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 367(3) and 4-phenylbutyl bromide; Yield: 40.4% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.36-1.55 (4H, m), 1.70-1.86 (6H, m), 2.68 (2H, t, J=7.2 Hz), 3.17-3.23 (2H, m), 4.04 (2H, t, J=6.6 Hz), 4.27-4.31 (1H, m), 6.63 (1H, d, J=8.1 Hz), 6.94 (1H, d, J=1.8 Hz), 7.07 (1H, dd, J=1.8, 8.1 Hz), 7.16-7.32 (7H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 367(4) and methyl chloroglyoxylate; Yield: 98.4% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.36-1.55 (4H, m), 1.57-1.65 (4H, m), 1.70-1.86 (2H, m), 2.59-2.62 (2H, m), 3.51-3.61 (4H, m), 3.98-4.04 (3H, m), 7.05-7.19 (6H, m), 7.22-7.31 (4H, m), 7.55-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 367(5); Yield: 89.0% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.87-0.91 (3H, m), 1.32-1.54 (8H, m), 1.67-1.76 (2H, m), 2.44-2.50 (2H, m), 3.15-3.26 (2H, m), 4.00-4.11 (2H, m), 7.08-7.29 (8H, m), 7.43-7.46 (2H, m), 7.79-7.82 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.87-0.91 (3H, m), 1.32-1.54 (8H, m), 1.67-1.76 (2H, m), 2.44-2.50 (2H, m), 3.60-3.67 (1H, m), 4.00-4.11 (3H, m), 7.08-7.29 (8H, m), 7.43-7.46 (2H, m), 7.81-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and cyclohexanol; Yield: 98% (pale brown oil).
1H-NMR (CDCl3) δ: 1.36-1.63 (4H, m), 1.64-1.77 (2H, m), 1.77-1.90 (2H, m), 1.90-2.02 (2H, m), 4.44-4.55 (1H, m), 7.16 (1H, d, J=9.0 Hz), 7.27-7.33 (2H, m), 7.53-7.59 (2H, m), 7.66 (1H, dd, J=2.7, 9.0 Hz), 7.98 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 368(1); Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 1.30-1.66 (6H, m), 1.75-1.87 (2H, m), 1.94-2.10 (2H, m), 3.89 (2H, brs), 4.22-4.35 (1H, m), 6.82-6.94 (3H, m), 7.19-7.25 (2H, m), 7.48-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 368(2) and 4-phenylbutyl bromide; Yield: 43% (colorless oil).
1H-NMR (CDCl3) δ: 1.28-1.47 (2H, m), 1.50-1.65 (4H, m), 1.67-1.85 (6H, m), 1.95-2.08 (2H, m), 2.68 (2H, t, J=6.6 Hz), 3.20 (2H, t, J=6.6 Hz), 4.21-4.30 (1H, m), 4.31 (1H, brs), 6.72-6.85 (3H, m), 7.14-7.32 (7H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 368(3) and methyl chloroglyoxylate; Yield: 66% (colorless oil).
1H-NMR (CDCl3) δ: 1.28-1.73 (10H, m), 1.73-1.87 (2H, m), 1.87-2.01 (2H, m), 2.51-2.67 (2H, m), 3.47-3.62 (1H, m), 3.53 (3H, s), 3.96-4.09 (1H, m), 4.29-4.40 (1H, m), 6.98 (1H, d, J=8.4 Hz), 7.08-7.30 (7H, m), 7.31 (1H, d, J=2.4 Hz), 7.43-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 368(4); Yield: 68% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.19-1.60 (10H, m), 1.60-1.77 (2H, m), 1.77-1.94 (2H, m), 3.20-3.50 (2H, m), 3.73-3.99 (2H, m), 4.33-4.50 (1H, m), 7.03-7.22 (6H, m), 7.33-7.49 (3H, m), 7.53-7.60 (2H, m), 7.63-7.71 (1H, m), 13.74 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.19-1.60 (10H, m), 1.60-1.77 (2H, m), 1.77-1.94 (2H, m), 3.20-3.50 (2H, m), 3.57-3.69 (2H, m), 4.33-4.50 (1H, m), 7.03-7.22 (6H, m), 7.33-7.49 (3H, m), 7.53-7.60 (2H, m), 7.63-7.71 (1H, m), 13.74 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 3-pentanol; Yield: 93% (yellow oil).
1H-NMR (CDCl3) δ: 1.00 (6H, t, J=7.5 Hz), 1.71-1.83 (4H, m), 4.34 (1H, quint, J=6.0 Hz), 7.13 (1H, d, J=9.0 Hz), 7.26-7.33 (2H, m), 7.51-7.59 (2H, m), 7.66 (1H, dd, J=2.4, 9.0 Hz), 7.97 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 369(1); Yield: 91% (pale brown solid).
1H-NMR (CDCl3) δ: 0.99 (6H, t, J=7.5 Hz), 1.67-1.79 (4H, m), 3.90 (2H, brs), 4.18 (1H, quint, J=6.0 Hz), 6.83 (1H, d, J=8.7 Hz), 6.88 (1H, dd, J=2.1, 8.7 Hz), 6.92 (1H, d, J=2.1 Hz), 7.19-7.25 (2H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 369(2) and 4-phenylbutyl bromide; Yield: 64% (colorless oil).
1H-NMR (CDCl3) δ: 0.97 (6H, t, J=7.8 Hz), 1.63-1.82 (8H, m), 2.68 (2H, t, J=7.2 Hz), 3.15-3.27 (2H, m), 4.16 (1H, quint, J=5.7 Hz), 4.28-4.37 (1H, m), 6.72-6.83 (3H, m), 7.10-7.34 (7H, m), 7.51-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 369(3) and methyl chloroglyoxylate; Yield: 78% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.8 Hz), 0.96 (3H, t, J=7.8 Hz), 1.58-1.77 (8H, m), 2.51-2.71 (2H, m), 3.32-3.50 (2H, m), 3.52 (3H, s), 4.05-4.30 (1H, m), 6.95 (1H, d, J=9.0 Hz), 7.07-7.28 (7H, m), 7.30 (1H, d, J=2.4 Hz), 7.44-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 369(4); Yield: 95% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.90 (6H, t, J=7.5 Hz), 1.38-1.72 (8H, m), 2.47-2.63 (2H, m), 3.31-3.48 (1H, m), 3.88-4.02 (1H, m), 4.34-4.45 (1H, m), 7.07-7.25 (6H, m), 7.40-7.49 (3H, m), 7.57-7.72 (3H, m), 13.66 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.90 (6H, t, J=7.5 Hz), 1.38-1.72 (8H, m), 2.47-2.63 (2H, m), 3.61 (1H, brs), 3.88-4.02 (1H, m), 4.28-4.43 (1H, m), 7.07-7.25 (6H, m), 7.40-7.49 (3H, m), 7.57-7.72 (3H, m), 13.66 (1H, brs).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 188(1) and piperidine; Yield: 93.9% (orange solid).
1H-NMR (CDCl3) δ: 1.56-1.68 (2H, m), 1.68-1.81 (4H, m), 3.00-3.14 (4H, m), 7.17 (1H, d, J=8.4 Hz), 7.23-7.34 (2H, m), 7.50-7.60 (2H, m), 7.63 (1H, dd, J=2.1. 8.4 Hz), 7.96 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 370(1); Yield: 80.3% (white solid).
1H-NMR (CDCl3) δ: 1.50-1.66 (2H, m), 1.66-1.79 (4H, m), 2.78-2.96 (4H, m), 4.05 (2H, s), 6.88-6.96 (2H, m), 7.04 (1H, d, J=9.0 Hz), 7.17-7.30 (2H, m), 7.49-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 370(2) and 4-phenylbutyl bromide; Yield: 35.3% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.40-1.92 (10H, m), 2.52-2.98 (6H, m), 3.12-3.25 (2H, m), 4.61-4.80 (1H, m), 6.72 (1H, d, J=2.1 Hz), 6.83 (1H, dd, J=2.1, 8.1 Hz), 7.02 (1H, d, J=8.1 Hz), 7.12-7.36 (7H, m), 7.50-7.61 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.40-1.92 (10H, m), 2.52-2.98 (6H, m), 3.24-3.34 (2H, m), 4.12-4.24 (1H, m), 6.72 (1H, d, J=2.1 Hz), 6.83 (1H, dd, J=2.1, 8.1 Hz), 7.02 (1H, d, J=8.1 Hz), 7.12-7.36 (7H, m), 7.50-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 370(3) and methyl chloroglyoxylate; Yield: 74.3% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.44-1.83 (10H, m), 2.48-2.68 (2H, m), 2.76-2.93 (2H, m), 3.05-3.22 (2H, m), 3.54-3.74 (4H, m), 4.18-4.34 (1H, m), 7.06-7.15 (4H, m), 7.15-7.23 (3H, m), 7.23-7.32 (2H, m), 7.42-7.54 (3H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.44-1.83 (10H, m), 2.48-2.68 (2H, m), 2.76-2.93 (2H, m), 3.05-3.22 (2H, m), 3.54-3.74 (4H, m), 3.86-3.95 (1H, m), 7.06-7.15 (4H, m), 7.15-7.23 (3H, m), 7.23-7.32 (2H, m), 7.42-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 370(4); Yield: 93.8% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ 1.10-1.80 (10H, m), 2.30-2.58 (2H, m), 2.60-2.76 (2H, m), 3.16-3.64 (3H, m), 3.92-4.12 (1H, m), 6.96-7.22 (6H, m), 7.36-7.55 (4H, m), 7.59-7.70 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ 1.10-1.80 (10H, m), 2.30-2.58 (2H, m), 2.95-3.18 (2H, m), 3.16-3.64 (3H, m), 3.68-3.85 (1H, m), 6.96-7.22 (6H, m), 7.36-7.55 (4H, m), 7.59-7.70 (2H, m).
A mixture of 4-chloro-2-nitrobenzaldehyde (1.856 g, 10.00 mmol), 4-(trifluoromethoxy)phenylboronic acid (3.089 g, 15.00 mmol), palladium(II) acetate (112 mg, 0.50 mmol), 2-(di-tert-butylphosphino)biphenyl (298 mg, 1.00 mmol), potassium fluoride (1.743 g, 30.00 mmol) and tetrahydrofuran (10 ml) was stirred at 70° C. for 30 minutes. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate, and filtered through Celite. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (2.542 mg, 82%) as a yellow solid.
1H-NMR (CDCl3) δ: 7.37-7.41 (2H, m), 7.67-7.73 (2H, m), 7.95-7.99 (1H, m), 8.07 (1H, d, J=8.1 Hz), 8.29 (1H, d, J=1.2 Hz), 10.46 (1H, s).
A mixture of the intermediate 371(1) (934 mg, 3.00 mmol), potassium carbonate (539 mg, 3.9 mmol), hexyltriphenylphosphonium bromide (1346 mg, 3.15 mmol), water (60 μl), sodium hydroxide (100 mg, 2.5 mmol) and 1,4-dioxane (4 ml) was refluxed for 1.5 hours. The reaction mixture was cooled to room temperature, and filtered. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15:1) to give the title compound (1.01 g, 89%) as a yellow liquid. This compound was obtained as a mixture of the geometric isomers.
E isomer: 1H-NMR (CDCl3) δ: 0.83-0.95 (3H, m), 1.22-1.57 (6H, m), 2.09-2.33 (2H, m), 6.31 (1H, dd, J=6.9, 15.6 Hz), 6.86 (1H, d, J=15.6 Hz), 7.30-7.77 (6H, m), 8.05-8.19 (1H, m).
Z isomer: 1H-NMR (CDCl3) δ: 0.83-0.95 (3H, m), 1.22-1.57 (6H, m), 2.09-2.33 (2H, m), 5.87 (1H, dd, J=7.5, 11.7 Hz), 6.71 (1H, d, J=11.7 Hz), 7.30-7.77 (6H, m), 8.05-8.19 (1H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 371(2); Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 0.85-0.92 (3H, m), 1.23-1.40 (8H, m), 1.59-1.70 (2H, m), 2.49-2.55 (2H, m), 3.65 (2H, brs), 6.86 (1H, d, J=1.5 Hz), 6.92 (1H, dd, J=1.5, 7.8 Hz), 7.11 (1H, d, J=7.8 Hz), 7.21-7.26 (2H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 371(3) and 4-phenylbutyl bromide; Yield: 56% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.86-0.92 (3H, m), 1.23-1.81 (14H, m), 2.43-2.49 (2H, m), 2.65-2.72 (2H, m), 3.20-3.26 (2H, m), 3.61 (1H, brs), 6.74 (1H, d, J=1.5 Hz), 6.84 (1H, dd, J=1.5, 7.8 Hz), 7.10 (1H, d, J=7.8 Hz), 7.13-7.31 (7H, m), 7.51-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 371(4) and methyl chloroglyoxylate; Yield: 80% (colorless oil).
1H-NMR (CDCl3) δ: 0.86-0.92 (3H, m), 1.23-1.73 (14H, m), 2.54-2.64 (4H, m), 3.05-3.18 (1H, m), 3.49 (3H, s), 4.25-4.30 (1H, m), 7.09-7.32 (8H, m), 7.39 (1H, d, J=7.8 Hz), 7.48-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 371(5); Yield: 57% (white solid).
1H-NMR (DMSO-d6) δ: 0.39-0.88 (3H, m), 1.18-1.60 (14H, m), 2.41-2.59 (4H, m), 2.95-4.22 (2H, m), 7.06-7.22 (5H, m), 7.31-7.49 (4H, m), 7.54-7.60 (1H, m), 7.67-7.77 (2H, m).
m-Chloroperbenzoic acid (3.24 g, 12.194 mmol) was added to a solution of 5-bromo-3-nitrosalicylaldehyde (2.00 g, 8.129 mmol) in dichloromethane (5 ml), and the mixture was stirred at room temperature for 2 hours. A saturated aqueous solution of sodium hydrogen sulfite was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. Methanol (15 ml) and catalytic amount of concentrated hydrochloric acid were added to the residue obtained by evaporation of the solvent under reduced pressure, and the mixture was stirred at room temperature for 1 hour. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (420 mg, 22%) as a white solid.
1H-NMR (CDCl3) δ: 7.37 (1H, d, J=2.1 Hz), 7.80 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 372(1) and 1-chloropentane; Yield: 35.4% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.90-1.05 (6H, m), 1.35-1.80 (12H, m), 3.99-4.11 (4H, m), 7.17 (1H, d, J=2.1 Hz), 7.43 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 372(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 76.8% (clear yellow oil).
1H-NMR (CDCl3) δ: 0.91-0.98 (6H, m), 1.35-1.57 (8H, m), 1.73-1.88 (4H, m), 4.08 (2H, t, J=6.6 Hz), 4.18 (2H, t, J=6.6 Hz), 7.21 (1H, d, J=2.1 Hz), 7.28-7.32 (2H, m), 7.46 (1H, d, J=2.1 Hz), 7.53-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 372(3); Yield: 68.2% (brown oil).
1H-NMR (CDCl3) δ: 0.91-0.98 (6H, m), 1.35-1.53 (8H, m), 1.75-1.88 (4H, m), 3.91 (2H, brs), 4.00-4.04 (4H, m), 6.48 (1H, d, J=2.1 Hz), 6.54 (1H, d, J=2.1 Hz), 7.21-7.24 (2H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 372(4) and 4-phenylbutyl bromide; Yield: 60.6% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.91-0.98 (6H, m), 1.35-1.49 (10H, m), 1.75-1.88 (6H, m), 2.62-2.71 (2H, m), 3.39-3.46 (2H, m), 3.98-4.06 (4H, m), 4.30-4.38 (1H, m), 6.41-6.44 (2H, m), 7.16-7.32 (7H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 372(5) and methyl chloroglyoxylate; Yield: 73.8% (clear colorless oil).
1H-NMR (CDCl3) δ: 0.91-0.98 (6H, m), 1.35-1.89 (16H, m), 2.52-2.61 (2H, m), 3.48-3.62 (4H, m), 4.00-4.28 (5H, m), 6.84 (1H, d, J=2.1 Hz), 7.05 (1H, d, J=2.1 Hz), 7.09-7.15 (3H, m), 7.18-7.23 (2H, m), 7.26-7.29 (2H, m), 7.45-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 372(6); Yield: 13.3% (clear yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.87-0.93 (6H, m), 1.32-1.49 (12H, m), 1.62-1.76 (4H, m), 2.44-2.50 (2H, m), 3.15-3.26 (2H, m), 4.00-4.11 (4H, m), 7.05-7.20 (7H, m), 7.42-7.45 (2H, m), 7.66-7.69 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.87-0.91 (6H, m), 1.32-1.54 (12H, m), 1.67-1.76 (4H, m), 2.44-2.50 (2H, m), 3.60-3.67 (1H, m), 4.00-4.11 (5H, m), 7.05-7.20 (7H, m), 7.42-7.45 (2H, m), 7.71-7.74 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and potassium tert-butoxide; Yield: 57.3% (yellow solid).
1H-NMR (CDCl3) δ: 1.46 (9H, s), 7.21-7.36 (3H, m), 7.52-7.61 (2H, m), 7.64 (1H, dd, J=2.4, 8.4 Hz), 7.90 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 373(1); Yield: 75.1% (white solid).
1H-NMR (CDCl3) δ: 1.43 (9H, s), 3.86 (2H, brs), 6.82 (1H, dd, J=2.4, 8.4 Hz), 6.90 (1H, d, J=2.4 Hz), 7.00 (1H, d, J=8.4 Hz), 7.17-7.27 (2H, m), 7.46-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 373(2) and 4-phenylbutyl bromide; Yield: 50.6% (pale yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.42 (9H, s), 1.63-1.85 (4H, m), 2.55-2.75 (2H, m), 3.10-3.25 (2H, m), 4.24-4.34 (1H, m), 6.70-6.78 (2H, m), 6.95-7.02 (1H, m), 7.09-7.34 (7H, m), 7.51-7.60 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.42 (9H, s), 1.63-1.85 (4H, m), 2.55-2.75 (2H, m), 3.10-3.25 (2H, m), 4.14-4.23 (1H, m), 6.70-6.78 (2H, m), 6.95-7.02 (1H, m), 7.09-7.34 (7H, m), 7.51-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 373(3) and methyl chloroglyoxylate; Yield: 56.6% (colorless oil).
1H-NMR (CDCl3) δ: 1.47 (9H, s), 1.55-1.75 (4H, m), 2.47-2.72 (2H, m), 3.47-3.66 (4H, m), 3.97-4.18 (1H, m), 7.04-7.38 (9H, m), 7.42 (1H, dd, J=2.4, 8.4 Hz), 7.45-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 373(4); Yield: 100% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.35-1.66 (13H, m), 2.40-2.67 (2H, m), 3.41-3.60 (1H, m), 3.82-4.02 (1H, m), 7.06-7.25 (5H, m), 7.30 (1H, d, J=8.7 Hz), 7.40-7.53 (3H, m), 7.59 (1H, dd, J=2.4, 8.7 Hz), 7.65-7.78 (2H, m), 13.70 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.35-1.66 (13H, m), 2.40-2.67 (2H, m), 3.60-3.71 (1H, m), 3.82-4.02 (1H, m), 7.06-7.25 (5H, m), 7.30 (1H, d, J=8.7 Hz), 7.40-7.53 (3H, m), 7.59 (1H, dd, J=2.4, 8.7 Hz), 7.65-7.78 (2H, m), 13.70 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 4-phenoxybutyl bromide; Yield: 29.6% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.30-1.56 (4H, m), 1.75-2.02 (6H, m), 3.20-3.38 (2H, m), 3.92-4.13 (4H, m), 4.26-4.42 (1H, m), 6.74-6.86 (3H, m), 6.86-6.99 (3H, m), 7.18-7.34 (4H, m), 7.49-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 374(1) and methyl chloroglyoxylate; Yield: 80.5% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.28-1.52 (4H, m), 1.66-1.93 (6H, m), 3.53 (3H, s), 3.56-3.72 (1H, m), 3.86-4.14 (5H, m), 6.76-6.86 (2H, m), 6.86-6.95 (1H, m), 7.00 (1H, d, J=8.4 Hz), 7.16-7.32 (4H, m), 7.39 (1H, d, J=2.1 Hz), 7.45-7.58 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 374(2); Yield: 71.9% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.87 (3H, t, J=6.9 Hz), 1.22-1.48 (4H, m), 1.48-1.84 (7H, m), 3.80-4.10 (5H, m), 6.76-6.93 (3H, m), 7.11-7.28 (3H, m), 7.35-7.48 (2H, m), 7.52-7.65 (2H, m), 7.65-7.78 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 1-pentadecanol; Yield: 63% (yellow oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.98-1.40 (22H, m), 1.42-1.64 (2H, m), 1.80-1.92 (2H, m), 4.14 (2H, t, J=6.6 Hz), 7.14 (1H, d, J=8.7 Hz), 7.26-7.34 (2H, m), 7.53-7.59 (2H, m), 7.69 (1H, dd, J=2.4, 8.7 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 375(1); Yield: 94% (gray solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.20-1.40 (22H, m), 1.42-1.64 (2H, m), 1.75-1.88 (2H, m), 3.89 (2H, brs), 4.03 (2H, t, J=6.6 Hz), 6.80-6.95 (3H, m), 7.19-7.26 (2H, m), 7.48-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 375(2) and 4-phenylbutyl bromide; Yield: 75% (gray solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.20-1.53 (24H, m), 1.72-1.95 (6H, m), 2.52-2.75 (2H, m), 3.16-3.23 (2H, m), 4.01 (2H, t, J=6.6 Hz), 4.27 (1H, brs), 6.70-6.82 (3H, m), 7.17-7.25 (7H, m), 7.49-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 375(3) and methyl chloroglyoxylate; Yield: 84% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.20-1.50 (24H, m), 1.52-1.85 (6H, m), 2.53-2.65 (2H, m), 3.47-3.60 (2H, m), 3.53 (3H, s), 3.88-4.07 (2H, m), 6.99 (1H, d, J=8.4 Hz), 7.06-7.30 (6H, m), 7.31 (1H, d, J=2.4 Hz), 7.45-7.53 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 375(4); Yield: 64% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.16-1.42 (24H, m), 1.52-1.74 (6H, m), 2.50-2.63 (2H, m), 3.69-3.82 (2H, m), 3.88-3.99 (2H, m), 6.90-6.98 (1H, m), 7.03-7.34 (7H, m), 7.40-7.54 (4H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 4-bromo-2-fluoronitrobenzene and 1-pentanol; Yield: 50% (yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.1 Hz), 1.35-1.50 (4H, m), 1.80-1.88 (2H, m), 4.09 (2H, t, J=6.5 Hz), 7.15 (1H, dd, J=2.0, 8.6 Hz), 7.22 (1H, d, J=2.0 Hz), 7.73 (1H, d, J=8.6 Hz).
Iron (1.13 g) and concentrated hydrochloric acid (6 ml) were added to a solution of the intermediate 376(1) (1.94 g, 6.73 mmol) in methanol (36 ml), and the mixture was refluxed for 2.5 hours. The reaction mixture was cooled to room temperature, and diluted with chloroform (150 ml). The organic layer was washed with a 5% aqueous solution of sodium hydrogen carbonate, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:chloroform=2:1) to give the title compound (938 mg, 54%) as a brown oil.
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.1 Hz), 1.37-1.47 (4H, m), 1.78-1.84 (2H, m), 3.78 (2H, brs), 3.96 (2H, t, J=6.4 Hz), 6.58 (1H, d, J=8.4 Hz), 6.87 (1H, s), 6.88 (1H, dd, J=2.0, 8.4 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 376(2) and 4-phenylbutyl bromide; Yield: 68% (yellow oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.1 Hz), 1.36-1.45 (4H, m), 1.67-1.83 (6H, m), 2.66 (2H, t, J=7.2 Hz), 3.10 (2H, brs), 3.94 (2H, t, J=6.6 Hz), 4.14 (1H, brs), 6.42 (1H, d, J=8.4 Hz), 6.82 (1H, d, J=2.2 Hz), 6.94 (1H, dd, J=2.0, 8.4 Hz), 7.15-7.21 (3H, m), 7.25-7.31 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 376(3) and methyl chloroglyoxylate; Yield: 90% (colorless syrup).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.0 Hz), 1.33-1.44 (3H, m), 1.51-1.68 (5H, m), 1.71-1.82 (2H, m), 2.52-2.63 (2H, m), 3.43-3.55 (1H, m), 3.56 (3H, s), 3.86-3.98 (3H, m), 6.94 (1H, d, J=8.8 Hz), 7.01-7.05 (2H, m), 7.09-7.28 (5H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 376(4) and 3-methyphenylboronic acid; Yield: 79% (colorless syrup).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.32-1.50 (4H, m), 1.55-1.70 (4H, m), 1.76-1.85 (2H, m), 2.43 (3H, s), 2.61 (2H, t, J=7.3 Hz), 3.48-3.61 (1H, m), 3.54 (3H, s), 3.93-4.07 (3H, m), 7.07-7.28 (9H, m), 7.33-7.39 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 376(5); Yield: 95% (colorless syrup).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.1 Hz), 1.32-1.42 (4H, m), 1.58-1.82 (6H, m), 2.43 (3H, s), 2.61 (2H, t, J=7.3 Hz), 3.70-3.81 (2H, m), 3.99 (2H, t, J=6.6 Hz), 7.07 (1H, s), 7.09-7.28 (8H, m), 7.31-7.39 (3H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 376(4) and 3-(trifluoromethyl)phenylboronic acid; Yield: 70% (colorless syrup).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.32-1.50 (4H, m), 1.55-1.72 (4H, m), 1.76-1.87 (2H, m), 2.57-2.65 (2H, m), 3.53-3.63 (1H, m), 3.57 (3H, s), 3.92-4.08 (3H, m), 7.07-7.28 (8H, m), 7.53-7.67 (2H, m), 7.74 (1H, d, J=7.5 Hz), 7.80 (1H, brs).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 377(1); Yield: 91% (colorless syrup).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.32-1.42 (4H, m), 1.58-1.78 (6H, m), 2.60 (2H, t, J=7.0 Hz), 3.77 (2H, t, J=6.8 Hz), 3.99 (2H, t, J=6.5 Hz), 7.05 (1H, brs), 7.09-7.27 (7H, m), 7.53-7.65 (2H, m), 7.74 (1H, d, J=7.5 Hz), 7.80 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 4-bromo-1-fluoro-2-nitrobenzene and 1-pentanol; Yield: 68.6% (clear brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.35-1.55 (4H, m), 1.79-1.86 (2H, m), 4.08 (2H, t, J=6.3 Hz), 6.96 (1H, d, J=9.0 Hz), 7.60 (1H, dd, J=2.4, 9.0 Hz), 7.95 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 378(1); Yield: 99.5% (brown solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.32-1.45 (4H, m), 1.76-1.81 (2H, m), 3.95 (2H, t, J=6.6 Hz), 4.31 (2H, brs), 6.62 (1H, d, J=8.4 Hz), 6.81 (1H, dd, J=2.4, 8.4 Hz), 6.87 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 378(2) and 4-phenylbutyl bromide; Yield: 58.8% (brown oil).
1H-NMR (CDCl3) δ: 0.90-0.94 (3H, m), 1.38-1.45 (4H, m), 1.68-1.81 (6H, m), 2.67 (2H, t, J=7.2 Hz), 3.10 (2H, t, J=6.0 Hz), 3.93 (2H, t, J=6.6 Hz), 4.19-4.27 (1H, m), 6.56 (1H, d, J=8.4 Hz), 6.64 (1H, d, J=2.1 Hz), 6.70 (1H, dd, J=2.1, 8.4 Hz), 7.16-7.31 (5H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 378(3) and methyl chloroglyoxylate; Yield: 54.5% (white solid).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.35-1.41 (4H, m), 1.55-1.62 (4H, m), 1.71-1.79 (2H, m), 2.58-2.63 (2H, m), 3.51-3.62 (4H, m), 3.86-3.96 (3H, m), 6.79 (1H, d, J=8.7 Hz), 7.11-7.29 (6H, m), 7.40 (1H, dd, J=2.7, 8.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 378(4) and 3-(trifluoromethyl)phenylboronic acid; Yield: 77% (colorless syrup).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.32-1.50 (4H, m), 1.55-1.72 (4H, m), 1.75-1.86 (2H, m), 2.56-2.64 (2H, m), 3.52-3.64 (1H, m), 3.55 (3H, s), 3.94-4.05 (3H, m), 7.01 (1H, d, J=8.6 Hz), 7.08-7.25 (5H, m), 7.36 (1H, d, J=2.2 Hz), 7.51-7.67 (4H, m), 7.72 (1H, brs).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 378(5); Yield: 99% (colorless syrup).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.1 Hz), 1.30-1.42 (4H, m), 1.57-1.78 (6H, m), 2.60 (2H, t, J=7.1 Hz), 3.73-3.83 (2H, m), 3.97 (2H, t, J=6.6 Hz), 6.98 (1H, d J=8.6 Hz), 7.07-7.25 (5H, m), 7.35 (1H, d, J=2.4 Hz), 7.49-7.60 (3H, m), 7.67 (1H, d, J=7.1 Hz), 7.75 (1H, s).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 378(4) and 3-methyphenylboronic acid; Yield: 71% (colorless syrup).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.32-1.50 (4H, m), 1.58-1.68 (4H, m), 1.74-1.85 (2H, m), 2.42 (3H, s), 2.60 (2H, t, J=6.4 Hz), 3.52-3.62 (1H, m), 3.53 (3H, s), 3.95-4.06 (3H, m), 6.97 (1H, d, J=8.6 Hz), 7.08-7.34 (9H, m), 7.35 (1H, d, J=2.4 Hz), 7.52 (1H, dd, J=2.4, 8.6 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 379(1); Yield: 95% (colorless syrup).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=6.4 Hz), 1.28-1.42 (4H, m), 1.58-1.77 (6H, m), 2.41 (3H, s), 2.59 (2H, t, J=6.9 Hz), 3.77 (2H, t, J=6.8 Hz), 3.94 (2H, t, J=6.6 Hz), 6.94 (1H, d, J=8.6 Hz), 7.07-7.37 (10H, m), 7.50 (1H, dd, J=2.2, 8.4 Hz).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-nonanol; Yield: 66% (brown oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.20-1.58 (12H, m), 1.82-1.94 (2H, m), 4.17 (2H, t, J=6.6 Hz), 7.13-7.22 (2H, m), 7.30-7.37 (2H, m), 7.56-7.64 (2H, m), 7.93 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 380(1); Yield: 98% (pale brown solid).
1H-NMR (CDCl3) δ: 0.80-0.93 (3H, m), 1.18-1.55 (12H, m), 1.74-1.89 (2H, m), 3.38 (2H, brs), 3.97-4.08 (2H, m), 6.71-6.80 (1H, m), 6.92-7.03 (2H, m), 7.16-7.27 (2H, m), 7.45-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 380(2) and 4-phenylbutyl bromide; Yield: 77% (pale brown solid).
1H-NMR (CDCl3) δ: 0.82-0.94 (3H, m), 1.18-1.88 (18H, m), 2.54-2.73 (2H, m), 3.11-3.25 (2H, m), 3.98-4.08 (2H, m), 4.29 (1H, brs), 6.63 (1H, d, J=8.1 Hz), 6.91-7.33 (9H, m), 7.48-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 380(3) and methyl chloroglyoxylate; Yield: 70% (pale brown oil).
1H-NMR (CDCl3) δ: 0.84-0.93 (3H, m), 1.20-1.53 (12H, m), 1.53-1.74 (4H, m), 1.75-1.86 (2H, m), 2.56-2.65 (2H, m), 3.52-3.63 (2H, m), 3.56 (3H, s), 3.94-4.08 (2H, m), 7.04-7.20 (6H, m), 7.20-7.33 (4H, m), 7.55-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 380(4); Yield: 95% (pale brown oil).
1H-NMR (CDCl3) δ: 0.84-0.92 (3H, m), 1.20-1.45 (12H, m), 1.52-1.78 (6H, m), 2.56-2.65 (2H, m), 3.68-3.89 (2H, m), 3.94-4.08 (2H, m), 6.76 (1H, d, J=2.1 Hz), 6.81 (1H, dd, J=2.1, 8.1 Hz), 7.08-7.30 (8H, m), 7.50-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 5,5,5-trifluoropentan-1-ol; Yield: 86% (pale yellow syrup).
1H-NMR (CDCl3) δ: 1.74-1.87 (2H, m), 1.88-2.03 (2H, m), 2.13-2.30 (2H, m), 4.18 (2H, t, J=5.9 Hz), 7.14 (1H, d, J=8.8 Hz), 7.31 (2H, d, J=7.9 Hz), 7.57 (2H, d, J=8.8 Hz), 7.71 (1H, dd, J=2.4, 8.8 Hz), 8.05 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 381(1); Yield: 75% (white solid).
1H-NMR (CDCl3) δ: 1.77-1.87 (2H, m), 1.87-1.98 (2H, m), 2.12-2.27 (2H, m), 3.88 (2H, brs), 4.06 (2H, t, J=6.0 Hz), 6.83 (1H, d, J=8.2 Hz), 6.88-6.94 (2H, m), 7.23 (2H, d, J=8.8 Hz), 7.52 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 381(2) and 4-phenylbutyl bromide; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.78-1.85 (6H, m), 1.85-1.97 (2H, m), 2.19-2.26 (2H, m), 2.68 (2H, t, J=7.1 Hz), 3.21 (2H, brs), 4.05 (2H, t, J=6.0 Hz), 4.21 (1H, brs), 6.74-6.81 (3H, m), 7.16-7.32 (7H, m), 7.54 (2H, d, J=8.6 Hz).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 381(3) and methyl chloroglyoxylate; Yield: 56% (colorless syrup).
1H-NMR (CDCl3) δ: 1.57-1.83 (6H, m), 1.83-1.93 (2H, m), 2.07-2.24 (2H, m), 2.61 (2H, t, J=7.1 Hz), 3.46-3.58 (1H, m), 3.53 (3H, s), 3.96-4.80 (3H, m), 6.99 (1H, d, J=8.7 Hz), 7.09-7.30 (7H, m), 7.32 (1H, d, J=2.2 Hz), 7.47-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 381(4); Yield: 100% (colorless syrup).
1H-NMR (CDCl3) δ: 1.59-1.74 (6H, m), 1.74-1.87 (2H, m), 2.02-2.18 (2H, m), 2.60 (2H, t, J=7.1 Hz), 3.68-3.85 (2H, m), 3.99 (2H, t, J=6.0 Hz), 6.96 (1H, d, J=8.6 Hz), 7.08-7.28 (7H, m), 7.32 (1H, d, J=2.2 Hz), 7.46-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 4-(4-fluorophenyl)butyl bromide; Yield: 45% (pale brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.33-1.52 (4H, m), 1.65-1.88 (6H, m), 2.65 (2H, t, J=6.9 Hz), 3.21 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 4.27 (1H, brs), 6.72-6.85 (3H, m), 6.92-7.00 (2H, m), 7.10-7.17 (2H, m), 7.20-7.27 (2H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 382(1) and methyl chloroglyoxylate; Yield: 68% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.30-1.50 (4H, m), 1.50-1.70 (4H, m), 1.74-1.85 (2H, m), 2.52-2.64 (2H, m), 3.48-3.62 (5H, m), 3.94-4.06 (2H, m), 6.72-6.85 (3H, m), 6.92-7.00 (2H, m), 7.10-7.17 (2H, m), 7.20-7.27 (2H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 382(2); Yield: 74% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.97 (3H, m), 1.24-1.43 (4H, m), 1.50-1.78 (6H, m), 2.50-2.62 (2H, m), 3.70-3.84 (2H, m), 3.95 (2H, t, J=6.3 Hz), 6.84-7.09 (5H, m), 7.20-7.33 (3H, m), 7.42-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 2-(trifluoromethyl)ethanol; Yield: 76.7% (pale yellow solid).
1H-NMR (CDCl3) δ: 2.69-2.84 (2H, m), 4.39 (2H, t, J=6.6 Hz), 7.18 (1H, d, J=8.8 Hz), 7.31-7.34 (2H, m), 7.56-7.61 (2H, m), 7.75 (1H, dd, J=2.4, 8.6 Hz), 8.06 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 383(1); Yield: 93.1% (gray solid).
1H-NMR (CDCl3) δ: 2.62-2.77 (2H, m), 3.91 (2H, brs), 4.30 (2H, t, J=6.2 Hz), 6.85 (1H, d, J=8.1 Hz), 6.90-6.95 (2H, m), 7.23-7.28 (2H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 383(2) and 4-phenylbutyl bromide; Yield: 58.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.69-1.80 (4H, m), 2.56-2.72 (4H, m), 3.20 (1H, brs), 4.18-4.29 (4H, m), 6.75-6.81 (3H, m), 7.23-7.31 (7H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 383(3) and methyl chloroglyoxylate; Yield: 83.0% (colorless oil).
1H-NMR (CDCl3) δ: 1.53-1.73 (4H, m), 2.53-2.75 (4H, m), 3.47-3.58 (1H, m), 3.54 (3H, s), 3.98-4.35 (3H, m), 7.01 (1H, d, J=8.6 Hz), 7.11-7.34 (8H, m), 7.47-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 383(4); Yield: 63.6% (colorless solid).
1H-NMR (CDCl3) δ: 1.60-1.70 (4H, m), 2.49-2.65 (4H, m), 3.70-3.85 (2H, m), 4.17-4.26 (2H, m), 6.98 (1H, d, J=8.6 Hz), 7.10-7.32 (8H, m), 7.49-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 4-(4-chlorophenyl)butyl bromide; Yield: 54% (pale brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.33-1.52 (4H, m), 1.65-1.88 (6H, m), 2.65 (2H, t, J=6.9 Hz), 3.21 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 4.27 (1H, brs), 6.71-6.83 (3H, m), 6.99-7.27 (6H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 384(1) and methyl chloroglyoxylate; Yield: 48% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.30-1.48 (4H, m), 1.51-1.68 (4H, m), 1.73-1.84 (2H, m), 2.52-2.64 (2H, m), 3.48-3.62 (5H, m), 3.92-4.07 (2H, m), 6.96-7.06 (3H, m), 7.16-7.21 (2H, m), 7.26-7.33 (3H, m), 7.46-7.53 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 384(2); Yield: 67% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.95 (3H, m), 1.26-1.41 (4H, m), 1.50-1.78 (6H, m), 2.50-2.59 (2H, m), 3.70-3.82 (2H, m), 3.94 (2H, t, J=6.6 Hz), 6.92-7.04 (3H, m), 7.12-7.32 (5H, m), 7.42-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-pentadecanol; Yield: 66% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.18-1.40 (22H, m), 1.40-1.59 (2H, m), 1.80-1.93 (2H, m), 4.12 (2H, t, J=6.6 Hz), 7.12-7.20 (2H, m), 7.30-7.37 (2H, m), 7.55-7.64 (2H, m), 7.93 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 385(1); Yield: 40% (white solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.18-1.40 (22H, m), 1.41-1.59 (2H, m), 1.76-1.90 (2H, m), 3.89 (2H, brs), 4.05 (2H, t, J=6.6 Hz), 6.77 (1H, d, J=8.1 Hz), 6.95-7.20 (2H, m), 7.19-7.27 (2H, m), 7.48-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 385(2) and 4-phenylbutyl bromide; Yield: 74% (brown oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.20-1.53 (24H, m), 1.65-1.89 (6H, m), 2.63-2.72 (2H, m), 3.15-3.25 (2H, m), 4.04 (2H, t, J=6.6 Hz), 4.30 (1H, brs), 6.63 (1H, d, J=8.4 Hz), 6.94 (1H, d, J=2.1 Hz), 7.07 (1H, dd, J=2.1, 8.4 Hz), 7.11-7.33 (7H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 385(3) and methyl chloroglyoxylate; Yield: 66% (pale brown oil).
1H-NMR (CDCl3) δ: 0.82-0.93 (3H, m), 1.20-1.50 (24H, m), 1.52-1.85 (6H, m), 2.55-2.66 (2H, m), 3.48-3.62 (2H, m), 3.56 (3H, s), 3.88-4.07 (2H, m), 7.01-7.20 (6H, m), 7.21-7.34 (4H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 385(4); Yield: 57% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.6 Hz), 1.10-1.45 (24H, m), 1.51-1.80 (6H, m), 2.53-2.65 (2H, m), 3.70-3.83 (2H, m), 3.97 (2H, t, J=6.6 Hz), 7.03 (1H, d, J=1.5 Hz), 7.06-7.34 (9H, m), 7.52-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-heptanol; Yield: 71% (brown oil).
1H-NMR (CDCl3) δ: 0.83-0.94 (3H, m), 1.20-1.56 (8H, m), 1.81-1.94 (2H, m), 4.12 (2H, t, J=6.3 Hz), 7.13-7.20 (2H, m), 7.30-7.37 (2H, m), 7.57-7.64 (2H, m), 7.93 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 386(1); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=6.6 Hz), 1.23-1.56 (8H, m), 1.78-1.90 (2H, m), 3.89 (2H, s), 4.05 (2H, t, J=6.3 Hz), 6.77 (1H, d, J=7.8 Hz), 6.93-7.04 (2H, m), 7.18-7.28 (2H, m), 7.47-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 386(2) and 4-phenylbutyl bromide; Yield: 75% (pale brown solid).
1H-NMR (CDCl3) δ: 0.85-0.94 (3H, m), 1.20-1.95 (14H, m), 2.57-2.73 (2H, m), 3.10-3.25 (2H, m), 4.04 (2H, t, J=6.6 Hz), 4.29 (1H, brs), 6.63 (1H, d, J=8.1 Hz), 6.94 (1H, d, J=2.1 Hz), 7.07 (1H, dd, J=2.1, 8.1 Hz), 7.13-7.33 (7H, m), 7.48-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 386(3) and methyl chloroglyoxylate; Yield: 64% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.85-0.94 (3H, m), 1.20-1.87 (14H, m), 2.57-2.67 (2H, m), 3.50-3.64 (2H, m), 3.56 (3H, s), 3.90-4.09 (2H, m), 7.02-7.20 (6H, m), 7.21-7.35 (4H, m), 7.54-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 386(4); Yield: 67% (colorless oil).
1H-NMR (CDCl3) δ: 0.81-0.97 (3H, m), 1.20-1.47 (8H, m), 1.55-1.79 (6H, m), 2.55-2.66 (2H, m), 3.73-3.83 (2H, m), 3.98 (2H, t, J=6.6 Hz), 7.00-7.34 (10H, m), 7.52-7.62 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and 1-nonanol; Yield: 68% (brown oil).
1H-NMR (CDCl3) δ: 0.84-0.92 (3H, m), 1.20-1.44 (12H, m), 1.71-1.83 (2H, m), 4.09 (2H, t, J=6.6 Hz), 7.00-7.06 (1H, m), 7.23-7.32 (2H, m), 7.53-7.60 (2H, m), 8.20-8.27 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 387(1); Yield: 40% (brown oil).
1H-NMR (CDCl3) δ: 0.84-0.92 (3H, m), 1.20-1.45 (12H, m), 1.57-1.70 (2H, m), 3.48 (2H, brs), 3.82 (2H, t, J=6.6 Hz), 6.63-6.70 (2H, m), 6.82 (1H, d, J=8.4 Hz), 7.17-7.25 (2H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 387(2) and 4-phenylbutyl bromide; Yield: 61% (brown oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.20-1.35 (12H, m), 1.53-1.85 (6H, m), 2.67 (2H, t, J=6.6 Hz), 3.11 (2H, t, J=6.6 Hz), 3.39 (1H, brs), 3.81 (2H, t, J=6.6 Hz), 6.53-6.60 (2H, m), 6.81-6.90 (1H, m), 7.14-7.33 (7H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 387(3) and methyl chloroglyoxylate; Yield: 83% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.20-1.42 (12H, m), 1.53-1.85 (6H, m), 2.61 (2H, t, J=6.6 Hz), 3.57 (3H, s), 3.77 (2H, t, J=6.6 Hz), 3.97 (2H, t, J=6.6 Hz), 6.88-6.95 (1H, m), 7.05-7.19 (5H, m), 7.19-7.28 (4H, m), 7.46-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 387(4); Yield: 77% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.20-1.42 (12H, m), 1.53-1.85 (6H, m), 2.60 (2H, t, J=6.6 Hz), 3.75 (2H, t, J=6.6 Hz), 3.96 (2H, t, J=6.6 Hz), 7.02-7.28 (10H, m), 7.45-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 2-chloro-5-nitrophenol and 1-bromononane; Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.59 (12H, m), 1.82-1.95 (2H, m), 4.12 (2H, t, J=6.6 Hz), 7.47-7.54 (1H, m), 7.73-7.82 (2H, m).
The title compound was obtained in the same manner as the Example 371(1) using the following starting materials.
Starting materials: the intermediate 388(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 76% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.44 (12H, m), 1.71-1.84 (2H, m), 4.08 (2H, t, J=6.6 Hz), 7.24-7.33 (2H, m), 7.44 (1H, d, J=8.1 Hz), 7.53-7.61 (2H, m), 7.83 (1H, d, J=2.1 Hz), 7.90 (1H, dd, J=2.1, 8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 388(2); Yield: 71% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.42 (12H, m), 1.65-1.77 (2H, m), 3.73 (2H, brs), 3.90 (2H, t, J=6.6 Hz), 6.31 (1H, d, J=1.8 Hz), 6.34 (1H, dd, J=1.8, 8.1 Hz), 7.00 (1H, d, J=8.1 Hz), 7.14-7.22 (2H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 388(3) and methyl chloroglyoxylate; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.42 (12H, m), 1.68-1.79 (2H, m), 3.95-4.03 (5H, m), 7.12 (1H, dd, J=2.1, 8.4 Hz), 7.20-7.26 (2H, m), 7.30 (1H, d, J=8.4 Hz), 7.51-7.59 (3H, m), 8.89 (1H, s).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 388(4) and 4-(tert-butyl)benzyl bromide; Yield: 23% (colorless oil).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.39 (21H, m), 1.58-1.70 (2H, m), 3.61 (3H, s), 3.73 (2H, t, J=6.3 Hz), 4.93 (2H, s), 6.55 (1H, d, J=1.8 Hz), 6.76 (1H, dd, J=1.8, 8.1 Hz), 7.15-7.27 (5H, m), 7.30-7.37 (2H, m), 7.47-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 388(5); Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.94 (3H, m), 1.20-1.35 (21H, m), 1.56-1.68 (2H, m), 3.71 (2H, t, J=6.3 Hz), 4.91 (2H, s), 6.50 (1H, d, J=1.8 Hz), 6.75 (1H, dd, J=1.8, 8.1 Hz), 7.15-7.27 (5H, m), 7.30-7.37 (2H, m), 7.48-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 388(3) and 4-phenylbutyl bromide; Yield: 28% (brown oil).
1H-NMR (CDCl3) δ: 0.85-0.93 (3H, m), 1.20-1.42 (12H, m), 1.61-1.83 (6H, m), 2.68 (2H, t, J=7.5 Hz), 3.16 (2H, t, J=6.9 Hz), 3.69 (1H, s), 3.90 (2H, t, J=6.6 Hz), 6.19 (1H, d, J=1.8 Hz), 6.25 (1H, dd, J=1.8, 8.1 Hz), 7.12 (1H, d, J=8.1 Hz), 7.14-7.34 (7H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 389(1) and methyl chloroglyoxylate; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.92 (3H, m), 1.19-1.42 (12H, m), 1.59-1.77 (6H, m), 2.63 (2H, t, J=6.6 Hz), 3.60 (3H, s), 3.77-3.94 (4H, m), 6.76 (1H, d, J=2.1 Hz), 6.81 (1H, dd, J=2.1, 7.8 Hz), 7.10-7.32 (8H, m), 7.50-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 389(2); Yield: 79% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.18-1.40 (12H, m), 1.53-1.73 (6H, m), 2.51-2.65 (2H, m), 3.70-3.90 (4H, m), 6.67-6.79 (2H, m), 7.02-7.27 (8H, m), 7.50-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 378(4) and 4-(trifluoromethyl)phenylboronic acid; Yield: 59% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.97 (3H, m), 1.22-1.51 (4H, m), 1.52-1.74 (4H, m), 1.74-1.87 (2H, m), 2.53-2.67 (2H, m), 3.48-3.62 (5H, m), 3.94-4.08 (2H, m), 7.01 (1H, d, J=8.4 Hz), 7.06-7.25 (5H, m), 7.38 (1H, d, J=1.8 Hz), 7.55 (1H, dd, J=1.8, 8.4 Hz), 7.55-7.62 (2H, m), 7.65-7.72 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 390(1); Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 0.85-0.97 (3H, m), 1.22-1.49 (4H, m), 1.52-1.88 (6H, m), 2.53-2.67 (2H, m), 3.70-3.88 (2H, m), 3.91-4.08 (2H, m), 6.98 (1H, d, J=8.4 Hz), 7.05-7.28 (5H, m), 7.33-7.39 (1H, m), 7.47-7.72 (5H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 378(4) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 39% (pale brown oil).
1H-NMR (CDCl3) δ: 0.84-0.97 (3H, m), 1.22-1.50 (4H, m), 1.52-1.74 (4H, m), 1.73-1.87 (2H, m), 2.53-2.67 (2H, m), 3.49-3.63 (5H, m), 3.94-4.08 (2H, m), 7.00 (1H, d, J=8.7 Hz), 7.07-7.25 (5H, m), 7.30-7.35 (2H, m), 7.37-7.49 (3H, m), 7.51 (1H, dd, J=2.1, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 391(1); Yield: 83% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.96 (3H, m), 1.22-1.43 (4H, m), 1.51-1.79 (6H, m), 2.53-2.64 (2H, m), 3.70-3.85 (2H, m), 3.89-4.00 (2H, m), 6.96 (1H, d, J=8.4 Hz), 7.05-7.26 (6H, m), 7.30-7.37 (2H, m), 7.38-7.46 (2H, m), 7.51 (1H, dd, J=2.1, 8.4 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 376(4) and 4-(trifluoromethyl)phenylboronic acid; Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.97 (3H, m), 1.23-1.50 (4H, m), 1.52-1.74 (4H, m), 1.74-1.87 (2H, m), 2.54-2.67 (2H, m), 3.50-3.64 (5H, m), 3.91-4.09 (2H, m), 7.07-7.29 (8H, m), 7.62-7.75 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 392(1); Yield: 73% (colorless oil).
1H-NMR (CDCl3) δ: 0.86-0.96 (3H, m), 1.26-1.46 (4H, m), 1.55-1.80 (6H, m), 2.56-2.67 (2H, m), 3.70-3.88 (2H, m), 3.94-4.05 (2H, m), 7.05-7.29 (8H, m), 7.62-7.75 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 376(4) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.97 (3H, m), 1.23-1.50 (4H, m), 1.52-1.74 (4H, m), 1.74-1.87 (2H, m), 2.53-2.67 (2H, m), 3.50-3.65 (5H, m), 3.96-4.08 (2H, m), 7.04-7.20 (5H, m), 7.20-7.36 (4H, m), 7.38-7.43 (1H, m), 7.45-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 393(1); Yield: 86% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.97 (3H, m), 1.33-1.45 (4H, m), 1.52-1.83 (6H, m), 2.54-2.67 (2H, m), 3.66-3.87 (2H, m), 3.94-4.08 (2H, m), 7.02-7.20 (9H, m), 7.37-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 211(1) and 1-heptanol; Yield: 94% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.80-0.94 (3H, m), 1.16-1.47 (8H, m), 1.68-1.83 (2H, m), 4.02-4.14 (2H, m), 6.96-7.05 (1H, m), 7.20-7.31 (2H, m), 7.50-7.59 (2H, m), 8.15-8.28 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 394(1); Yield: 42% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.18-1.38 (8H, m), 1.55-1.69 (2H, m), 3.49 (2H, brs), 3.82 (2H, t, J=6.3 Hz), 6.62-6.70 (2H, m), 6.80-6.86 (1H, m), 7.17-7.25 (2H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 394(2) and 4-phenylbutyl bromide; Yield: 59% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.17-1.38 (8H, m), 1.51-1.79 (6H, m), 2.61-2.70 (2H, m), 3.07-3.17 (2H, m), 3.39 (1H, brs), 3.81 (2H, t, J=6.3 Hz), 6.53-6.60 (2H, m), 6.82-6.89 (1H, m), 7.13-7.32 (7H, m), 7.50-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 394(3) and methyl chloroglyoxylate; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.19-1.43 (8H, m), 1.51-1.79 (6H, m), 2.56-2.66 (2H, m), 3.57 (3H, s), 3.73-3.80 (2H, m), 3.97 (2H, t, J=6.3 Hz), 6.91 (1H, d, J=8.4 Hz), 7.07-7.19 (5H, m), 7.19-7.29 (4H, m), 7.47-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 394(4); Yield: 82% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.92 (3H, m), 1.18-1.43 (8H, m), 1.50-1.79 (6H, m), 2.52-2.65 (2H, m), 3.69-3.80 (2H, m), 3.96 (2H, t, J=6.3 Hz), 6.91 (1H, d, J=8.4 Hz), 7.07-7.19 (5H, m), 7.19-7.29 (4H, m), 7.47-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: methyl 5-bromosalicylate and benzyl bromide; Yield: 99% (colorless oil).
1H-NMR (CDCl3) δ: 3.90 (3H, s), 5.17 (2H, s), 6.89 (1H, d, J=9.0 Hz), 7.32-7.54 (6H, m), 7.93 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 401(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 54% (white solid).
1H-NMR (CDCl3) δ: 3.94 (3H, s), 5.24 (2H, s), 7.09 (1H, d, J=8.7 Hz), 7.24-7.44 (5H, m), 7.47-7.53 (2H, m), 7.53-7.59 (2H, m), 7.62 (1H, dd, J=2.4, 8.7 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 401(2); Yield: 91% (white solid).
1H-NMR (DMSO-d6) δ: 5.35 (2H, s), 7.22 (1H, d, J=8.7 Hz), 7.27-7.32 (2H, m), 7.41-7.50 (5H, m), 7.56-7.64 (2H, m), 7.75 (1H, dd, J=2.4, 8.4 Hz), 8.43 (1H, d, J=2.4 Hz), 10.78 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 2,5-dihydroxybenzaldehyde and 4-(trifluoromethoxy)benzyl bromide; Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 5.05 (2H, s), 5.16 (2H, s), 7.00 (1H, d, J=9.0 Hz), 7.17-7.27 (5H, m), 7.43-7.48 (5H, m), 10.50 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 403(1) and malonic acid; Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 5.04 (2H, s), 5.11 (2H, s), 6.49 (1H, d, J=15.9 Hz), 6.88 (1H, d, J=8.7 Hz), 6.96 (1H, dd, J=3.0, 8.7 Hz), 7.17 (1H, d, J=3.0 Hz), 7.23-7.28 (4H, m), 7.42-7.48 (4H, m), 8.13 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 403; Yield: 39% (white solid).
1H-NMR (CDCl3) δ: 2.68 (2H, t, J=7.8 Hz), 2.98 (2H, t, J=7.8 Hz), 4.99 (2H, s), 5.04 (2H, s), 6.75 (1H, dd, J=3.0, 8.7 Hz), 6.80 (1H, d, J=8.7 Hz), 6.86 (1H, d, J=3.0 Hz), 7.22-7.26 (4H, m), 7.43-7.46 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 1-chlorobutane; Yield: 97% (brown oil).
1H-NMR (CDCl3) δ: 1.01 (3H, t, J=7.5 Hz), 1.51-1.59 (2H, m), 1.84-1.89 (2H, m), 4.14 (2H, t, J=6.3 Hz), 7.07 (1H, d, J=8.7 Hz), 7.27 (2H, d, J=8.1 Hz), 7.56-7.59 (2H, m), 7.74 (1H, dd, J=2.7, 8.7 Hz), 8.04 (1H, d, J=2.7 Hz), 10.55 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting material.
Starting material: the intermediate 405(1) and malonic acid; Yield: 74% (white solid).
1H-NMR (CDCl3) δ: 1.02 (3H, t, J=7.2 Hz), 1.52-1.59 (2H, m), 1.86-1.95 (2H, m), 4.10 (2H, t, J=6.6 Hz), 6.64 (1H, d, J=16.2 Hz), 7.00 (1H, d, J=8.4 Hz), 7.28 (2H, d, J=7.8 Hz), 7.55-7.58 (3H, m), 7.71 (1H, d, J=2.4 Hz), 8.13 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 1-chloropentane; Yield: 91% (brown oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.2 Hz), 1.38-1.55 (4H, m), 1.84-1.93 (2H, m), 4.13 (2H, t, J=6.6 Hz), 7.07 (1H, d, J=8.7 Hz), 7.27 (2H, d, J=7.8 Hz), 7.56-7.59 (2H, m), 7.74 (1H, dd, J=2.4, 8.7 Hz), 8.04 (1H, d, J=2.4 Hz), 10.56 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 406(1) and malonic acid; Yield: 67% (white solid).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.39-1.53 (4H, m), 1.86-1.95 (2H, m), 4.10 (2H, t, J=6.6 Hz), 6.65 (1H, d, J=16.2 Hz), 7.00 (1H, d, J=8.4 Hz), 7.28 (2H, d, J=8.7 Hz), 7.52-7.58 (3H, m), 7.71 (1H, d, J=2.4 Hz), 8.13 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 405; Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.2 Hz), 1.45-1.56 (2H, m), 1.76-1.86 (2H, m), 2.71 (2H, t, J=7.8 Hz), 3.01 (2H, t, J=7.8 Hz), 4.02 (2H, t, J=6.3 Hz), 6.90 (1H, d, J=9.0 Hz), 7.24 (2H, d, J=8.7 Hz), 7.35-7.39 (2H, m), 7.51-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 406; Yield: 75% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.9 Hz), 1.36-1.52 (4H, m), 1.78-1.88 (2H, m), 2.72 (2H, t, J=7.8 Hz), 3.01 (2H, t, J=7.8 Hz), 4.01 (2H, t, J=6.3 Hz), 6.89 (1H, d, J=9.0 Hz), 7.24 (2H, d, J=8.7 Hz), 7.35-7.39 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 3,5-dihydroxybenzaldehyde and 4-(tert-butyl)benzyl bromide; Yield: 21% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.05 (2H, s), 5.51 (1H, brs), 6.74-6.76 (1H, m), 6.96-6.98 (1H, m), 7.08-7.09 (1H, m), 7.34-7.44 (4H, m), 9.87 (1H, s).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: the intermediate 409(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 93% (yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, m), 5.06 (2H, s), 6.86-6.87 (1H, m), 7.02-7.09 (3H, m), 7.20-7.26 (3H, m), 7.33-7.44 (4H, m), 9.90 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 409(2) and malonic acid; Yield: 84% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.02 (2H, s), 6.37 (1H, d, J=15.9 Hz), 6.65-6.67 (1H, m), 6.78 (1H, brs), 6.92 (1H, brs), 7.00-7.03 (2H, m), 7.18-7.22 (2H, m), 7.32-7.43 (4H, m), 7.67 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 409; Yield: 97% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.65 (2H, t, J=7.7 Hz), 2.89 (2H, t, J=7.7 Hz), 4.95 (2H, s), 6.46-6.47 (2H, m), 6.61 (1H, brs), 6.95-7.00 (2H, m), 7.14-7.18 (2H, m), 7.30-7.41 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 5-nitrosalicylaldehyde and 4-(tert-butyl)benzyl bromide; Yield: 92% (yellow solid).
1H-NMR (CDCl3): δ 1.34 (9H, s), 5.29 (2H, s), 7.19 (1H, d, J=9.2 Hz), 7.36-7.48 (4H, m), 8.41 (1H, dd, J=2.9, 9.2 Hz), 8.72 (1H, d, J=2.9 Hz), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 26(1) using the following starting materials.
Starting materials: the intermediate 411(1); Yield: 81% (yellow solid).
1H-NMR (CDCl3) δ: 1.32 (3H, t, J=7.1 Hz), 1.33 (9H, s), 4.27 (2H, q, J=7.1 Hz), 5.25 (2H, s), 6.62 (1H, d, J=16.1 Hz), 7.04 (1H, d, J=9.1 Hz), 7.33-7.47 (4H, m), 8.02 (1H, d, J=16.1 Hz), 8.20 (1H, dd, J=2.7, 9.1 Hz), 8.44 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 411(2); Yield: 86% (brown oil).
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.1 Hz), 1.33 (9H, s), 2.60 (2H, t, J=7.8 Hz), 2.92 (2H, t, J=7.8 Hz), 3.38 (2H, brs), 4.11 (2H, q, J=7.1 Hz), 4.97 (2H, s), 6.51 (1H, dd, J=2.9, 8.4 Hz), 6.57 (1H, d, J=2.9 Hz), 6.74 (1H, d, J=8.4 Hz), 7.33-7.41 (4H, m).
Triethylamine (0.265 ml, 1.901 mmol) was added dropwise to a mixture of the intermediate 411(3) (561 mg, 1.579 mmol), 4-(trifluoromethoxy)benzoyl chloride (0.300 ml, 1.903 mmol) and dichloromethane (3.0 ml) at 0° C., and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (0.669 g, 78%) as a white solid.
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.1 Hz), 1.34 (9H, s), 2.65 (2H, t, J=7.7 Hz), 3.00 (2H, t, J=7.7 Hz), 4.11 (2H, q, J=7.1 Hz), 5.07 (2H, s), 6.89-6.92 (1H, m), 7.29-7.43 (7H, m), 7.50-7.54 (1H, m), 7.72 (1H, brs), 7.88-7.91 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 411(4); Yield: 71% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.49-2.54 (2H, m), 2.80-2.85 (2H, m), 5.09 (2H, s), 7.02-7.05 (1H, m), 7.37-7.44 (4H, m), 7.51-7.60 (4H, m), 8.05-8.08 (2H, m), 10.20 (1H, s), 12.15 (1H, brs).
A mixture of the intermediate 411(3) (625 mg, 1.758 mmol), 4-(trifluoromethoxy)phenylboronic acid (724 mg, 3.517 mmol), anhydrous copper(II) acetate (319 mg, 1.759 mmol), triethylamine (0.490 ml, 3.515 mmol) and dichloromethane (9 ml) was stirred at room temperature for 4 days. The reaction mixture was filtered through Celite. After the filtrate was washed with a 5% aqueous solution of ammonia and saturated brine, the organic layer was dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (399 mg, 44%) as a brown oil.
1H-NMR (CDCl3) δ: 1.21 (3H, t, J=7.1 Hz), 1.34 (9H, s), 2.63 (2H, t, J=7.7 Hz), 2.97 (2H, t, J=7.7 Hz), 4.10 (2H, q, J=7.1 Hz), 5.04 (2H, s), 5.49 (1H, brs), 6.83-6.87 (3H, m), 6.92-7.08 (4H, m), 7.35-7.44 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 412(1); Yield: 65% (brown solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.49-2.53 (2H, m), 2.77-2.82 (2H, m), 5.05 (2H, s), 6.90-7.00 (5H, m), 7.12-7.15 (2H, m), 7.36-7.44 (4H, m), 8.06 (1H, s), 12.12 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-hydroxybenzaldehyde and 4-(trifluoromethoxy)benzyl bromide acid; Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 5.14 (2H, s), 7.06-7.09 (2H, m), 7.24-7.27 (2H, m), 7.45-7.48 (2H, m), 7.84-7.88 (2H, m), 9.90 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 413(1); Yield: 65% (yellow solid).
1H-NMR (CDCl3) δ: 4.99 (2H, s), 6.74-6.78 (2H, m), 6.83-6.86 (2H, m), 7.22 (2H, d, J=8.0 Hz), 7.42-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 83(2) using the following starting material.
Starting material: the intermediate 413(2); Yield: 57% (pale yellow solid).
1H-NMR (CDCl3) δ: 5.05 (2H, s), 6.95 (1H, d, J=9.0 Hz), 7.07 (1H, d, J=3.0 Hz), 7.21 (1H, dd, J=3.0, 9.0 Hz), 7.24 (2H, d, J=7.5 Hz), 7.44-7.47 (2H, m), 9.84 (1H, s), 10.68 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 413(3) and 4-(tert-butyl)benzyl bromide; Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.04 (2H, s), 5.12 (2H, s), 7.04 (1H, d, J=9.0 Hz), 7.18 (1H, dd, J=3.0, 9.0 Hz), 7.22-7.26 (2H, m), 7.36 (2H, d, J=8.5 Hz), 7.41-7.47 (5H, m), 10.50 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 413(4) and malonic acid; Yield: 78% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.03 (2H, s), 5.08 (2H, s), 6.49 (1H, d, J=16.0 Hz), 6.90-6.98 (2H, m), 7.16 (1H, d, J=2.5 Hz), 7.22-7.26 (2H, m), 7.33-7.36 (2H, m), 7.39-7.47 (4H, m), 8.13 (1H, d, J=16.0 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 413; Yield: 84% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.68 (2H, t, J=7.5 Hz), 2.97 (2H, t, J=7.5 Hz), 4.98 (2H, s), 5.00 (2H, s), 6.75 (1H, dd, J=3.0, 9.0 Hz), 6.84 (1H, d, J=9.0 Hz), 6.85 (1H, d, J=3.0 Hz), 7.22 (2H, d, J=8.0 Hz), 7.32-7.46 (6H, m).
Triethylamine (0.120 ml, 0.861 mmol) was added dropwise to a mixture of the intermediate 411(3) (237 mg, 0.667 mmol), 4-(trifluoromethoxy)benzenesulfonyl chloride and dichloromethane (1.5 ml) at 0° C., and the mixture was stirred at room temperature for 15 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (306 mg, 79%) as a pale pink solid.
1H-NMR (CDCl3) δ: 1.21 (3H, t, J=7.1 Hz), 1.33 (9H, s), 2.53 (2H, t, J=7.5 Hz), 2.89 (2H, t, J=7.5 Hz), 4.08 (2H, q, J=7.1 Hz), 5.01 (2H, s), 6.39 (1H, brs), 6.77-6.90 (3H, m), 7.23-7.27 (2H, m), 7.31-7.42 (4H, m), 7.72-7.75 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 415(1); Yield: 37% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.38 (2H, t, J=7.6 Hz), 2.70 (2H, t, J=7.6 Hz), 4.99 (2H, s), 6.81-6.93 (3H, m), 7.32-7.41 (4H, m), 7.52-7.55 (2H, m), 7.78-7.82 (2H, m), 9.99 (1H, s), 12.10 (1H, s).
A mixture of the intermediate 411(3) (1.157 g, 3.255 mmol), iodomethane (0.250 ml, 4.016 mmol), potassium carbonate (555 mg, 4.016 mmol) and dimethylformamide (6.5 ml) was stirred at 40° C. for 20 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (352 mg, 29%) as a brown oil.
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.1 Hz), 1.33 (9H, s), 2.61 (2H, t, J=7.8 Hz), 2.79 (3H, s), 2.95 (2H, t, J=7.8 Hz), 3.43 (1H, brs), 4.11 (2H, q, J=7.1 Hz), 4.98 (2H, s), 6.44 (1H, dd, J=2.9, 8.6 Hz), 6.51 (1H, d, J=2.9 Hz), 6.80 (1H, d, J=8.6 Hz), 7.34-7.42 (4H, m).
The title compound was obtained in the same manner as the Example 411(4) using the following starting materials.
Starting materials: the intermediate 416(1) and 4-(trifluoromethoxy)benzoyl chloride; Yield: 49% (brown oil).
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.1 Hz), 1.33 (9H, s), 2.47 (2H, t, J=7.6 Hz), 2.87 (2H, t, J=7.6 Hz), 3.44 (3H, s), 4.08 (2H, q, J=7.1 Hz), 4.99 (2H, s), 6.72-6.89 (3H, m), 6.99-7.02 (2H, m), 7.29-7.42 (6H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 416(2); Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.54 (2H, t, J=7.4 Hz), 2.87 (2H, t, J=7.4 Hz), 3.43 (3H, s), 4.99 (2H, s), 6.71-6.89 (3H, m), 6.99-7.02 (2H, m), 7.28-7.41 (6H, m).
The title compound was obtained in the same manner as the Example 412(1) using the following starting materials.
Starting materials: the intermediate 416(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 39% (brown oil).
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.1 Hz), 1.34 (9H, s), 2.63 (2H, t, J=7.7 Hz), 2.97 (2H, t, J=7.7 Hz), 3.23 (3H, s), 4.08 (2H, q, J=7.1 Hz), 5.06 (2H, s), 6.67-6.71 (2H, m), 6.88-7.03 (5H, m), 7.36-7.44 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 417(1); Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.69 (2H, t, J=7.6 Hz), 2.97 (2H, t, J=7.6 Hz), 3.23 (3H, s), 5.06 (2H, s), 6.68-6.71 (2H, m), 6.89-7.04 (5H, m), 7.35-7.44 (4H, m).
A mixture of 1-bromo-4-(trifluoromethoxy)benzene (711 mg, 2.95 mmol), 1-(tert-buthoxycarbonyl)piperadine (500 mg, 2.68 mmol), sodium tert-butoxide (515 mg, 5.36 mmol), tris(dibenzylideneacetone)dipalladium(0) (245 mg, 0.26 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (333 mg, 0.53 mmol) and toluene (10 ml) was stirred at 100° C. for 4 hours. After the reaction mixture was filtered, the residue obtained by concentration of the filtrate was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1) to give the title compound (1.03 g, 100%) as a yellow solid.
1H-NMR (CDCl3) δ: 1.49 (9H, s), 3.11 (4H, t, J=5.1 Hz), 3.58 (4H, t, J=5.1 Hz), 6.87-6.91 (2H, m), 7.10-7.14 (2H, m).
A mixture of the intermediate 418(1) (1.03 g, 2.97 mmol), ethyl acetate (10 ml) and 4 N hydrochloric acid-ethyl acetate (10 ml) was stirred at room temperature for 1 hour. The precipitated solid was collected by filtration to give the title compound (773 mg, 92%) as a white solid.
1H-NMR (DMSO-d6) δ: 3.21 (4H, brs), 3.37-3.40 (4H, m), 7.07 (2H, d, J=9.3 Hz), 7.25 (2H, d, J=9.3 Hz), 9.13 (1H, brs).
The title compound was obtained in the same manner as the Example 418(1) using the following starting materials.
Starting materials: the intermediate 4(1) and the intermediate 418(2); Yield: 13% (orange solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 3.27-3.33 (8H, m), 5.13 (2H, s), 6.93-6.96 (2H, m), 7.03-7.06 (1H, m), 7.13-7.16 (2H, m), 7.20-7.27 (2H, m), 7.35-7.38 (2H, m), 7.41-7.45 (2H, m), 10.53 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 418(3) and malonic acid; Yield: 60% (yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.23-3.27 (4H, m), 3.32-3.35 (4H, m), 5.10 (2H, s), 6.54 (1H, d, J=16.2 Hz), 6.92-7.04 (4H, m), 7.13-7.18 (3H, m), 7.34-7.43 (4H, m), 8.14 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 418; Yield: 56% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 2.80 (2H, t, J=7.8 Hz), 3.13-3.15 (4H, m), 3.27-3.32 (6H, m), 5.02 (2H, s), 6.78 (1H, dd, J=2.7, 9.0 Hz), 6.88-6.94 (2H, m), 7.06 (2H, d, J=8.7 Hz), 7.21 (2H, d, J=8.7 Hz), 7.34-7.42 (4H, m), 12.12 (1H, brs).
Sodium hydroxide (183 mg, 4.584 mg) was added to a mixture of the intermediate 6(3) (238 mg, 0.573 mmol), 1,1,1-trichloro-2-methyl-2-propanol (203 mg, 1.146 mmol) and acetone (3 ml) at 0° C., and the mixture was stirred at room temperature for 2 hours. The reaction mixture was cooled to 0° C., acidified by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with a mixture of n-hexane and diisopropyl ether to give the title compound (105 mg, 37%) as a white solid.
1H-NMR (CDCl3) δ: 1.29 (9H, s), 1.48 (6H, s), 5.13 (2H, s), 6.72-6.79 (2H, m), 6.96 (1H, d, J=7.8 Hz), 7.36-7.46 (6H, m), 7.61 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: methyl 5-iodosalicylate and 4-(tert-butyl)benzyl bromide; Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.90 (3H, s), 5.13 (2H, s), 6.79 (1H, d, J=9.0 Hz), 7.35-7.44 (4H, m), 7.69 (1H, dd, J=2.5, 9.0 Hz), 8.09 (1H, d, J=2.5 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting material.
Starting material: the intermediate 421(1); Yield: 54% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.94 (3H, s), 5.21 (2H, s), 7.11 (1H, d, J=8.7 Hz), 7.24-7.31 (2H, m), 7.38-7.48 (4H, m), 7.53-7.60 (2H, m), 7.63 (1H, dd, J=2.4, 8.7 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 421(2); Yield: 99% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 5.18 (2H, s), 7.23 (1H, d, J=8.7 Hz), 7.35-7.46 (6H, m), 7.67-7.78 (3H, m), 7.80 (1H, d, J=2.4 Hz).
A 1.65 M solution of n-Butyllithium in hexane (345 μL, 0.570 mmol) was added dropwise to a solution of the compound 12 (130 mg, 0.285 mmol) in anhydrous tetrahydrofuran (2 ml) at −78° C., and the mixture was stirred for 30 minutes. A small portion of trifluoroacetic acid was added to the reaction mixture, and the mixture was left at room temperature. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (35 mg, 24%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=6.9 Hz), 1.23-1.38 (11H, m), 1.50-1.70 (4H, m), 2.80-3.00 (3H, m), 6.87 (1H, d, J=8.4 Hz), 6.91 (2H, m), 7.21-7.28 (2H, m), 7.31 (1H, dd, J=2.1, 8.4 Hz), 7.34-7.38 (2H, m), 7.41 (1H, d, J=2.1 Hz), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 5-bromo-2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99% (brown oil).
1H-NMR (CDCl3) δ: 7.33-7.43 (3H, m), 7.57-7.62 (2H, m), 7.79-7.84 (1H, m), 8.23 (1H, dd, J=2.4, 6.9 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 423(1) and 4-(tert-butyl)phenol; Yield: 100% (whitish-pink solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.01-7.04 (2H, m), 7.08 (1H, d, J=8.4 Hz), 7.30-7.34 (2H, m), 7.40-7.43 (2H, m), 7.56-7.59 (2H, m), 7.65 (1H, dd, J=2.4, 8.4 Hz), 8.13 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 423(2); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.91 (2H, brs), 6.85-7.00 (5H, m), 7.24-7.26 (2H, m), 7.33-7.36 (2H, m), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 423(3) and ethyl 2-bromohexanoate; Yield: 34% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.85-0.91 (3H, m), 1.22-1.56 (16H, m), 1.74-1.89 (2H, m), 4.08-4.24 (3H, m), 4.73 (1H, brs), 6.79-6.89 (3H, m), 6.96-7.02 (2H, m), 7.23-7.27 (2H, m), 7.33-7.38 (2H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 423(4); Yield: 53% (white solid).
1H-NMR (DMSO-d6) δ: 0.78-0.83 (3H, m), 1.23-1.28 (13H, m), 1.52-1.57 (2H, m), 4.21-4.23 (1H, m), 5.10 (1H, brs), 6.83-6.96 (5H, m), 7.36-7.45 (4H, m), 7.70-7.74 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 301(2) and 1-chloropentane; Yield: 76% (yellow oil).
1H-NMR (CDCl3) δ: 0.88-0.95 (9H, m), 1.31-1.49 (12H, m), 1.78-1.87 (6H, m), 4.04 (4H, t, J=6.6 Hz), 4.20 (2H, t, J=6.9 Hz), 4.65 (2H, s), 6.69 (2H, s), 7.25-7.27 (2H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 424(1); Yield: 23% (white solid).
1H-NMR (DMSO-d6) δ: 0.89 (6H, t, J=6.9 Hz), 1.31-1.42 (8H, m), 1.68-1.74 (4H, m), 4.01-4.08 (6H, m), 6.86 (2H, s), 7.39-7.41 (2H, m), 7.75-7.78 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 301(2) and 1-chloroheptane; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 0.88-0.95 (9H, m), 1.31-1.49 (24H, m), 1.78-1.87 (6H, m), 4.04 (4H, t, J=6.6 Hz), 4.20 (2H, t, J=6.9 Hz), 4.65 (2H, s), 6.69 (2H, s), 7.25-7.27 (2H, m), 7.51-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 425(1); Yield: 23% (white solid).
1H-NMR (DMSO-d6) δ: 0.86 (6H, t, J=6.9 Hz), 1.28-1.38 (16H, m), 1.67-1.74 (4H, m), 4.01-4.08 (6H, m), 6.86 (2H, s), 7.39-7.41 (2H, m), 7.75-7.78 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 1-bromo-3,5-dimethoxybenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 95% (pale brown oil).
1H-NMR (CDCl3) δ: 3.85 (6H, s), 6.48 (1H, t, J=2.4 Hz), 6.68 (2H, d, J=2.4 Hz), 7.20-7.33 (2H, m), 7.52-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 83(1) using the following starting material.
Starting material: the intermediate 426(1); Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 5.04 (2H, s), 6.36 (1H, t, J=2.1 Hz), 6.60 (2H, d, J=2.1 Hz), 7.20-7.31 (2H, m), 7.50-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 426(2) and ethyl 2-bromohexanoate; Yield: 24% (pale brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30-1.62 (4H, m), 1.86-2.04 (2H, m), 4.24 (2H, q, J=7.2 Hz), 4.58-4.67 (2H, m), 6.38 (1H, t, J=2.1 Hz), 6.60-6.70 (2H, m), 7.20-7.30 (2H, m), 7.47-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: the intermediate 426(3) and 4-(tert-butyl)phenylboronic acid; Yield: 6% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.18-1.62 (16H, m), 1.84-2.04 (2H, m), 4.21 (2H, q, J=7.2 Hz), 4.55-4.65 (1H, m), 6.47-6.54 (1H, m), 6.75-6.85 (2H, m), 6.93-7.03 (2H, m), 7.20-7.30 (2H, m), 7.31-7.40 (2H, m), 7.45-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 426(4); Yield: 85% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.2 Hz), 1.20-1.62 (13H, m), 1.90-2.06 (2H, m), 4.68 (1H, t, J=6.0 Hz), 6.50-6.58 (1H, m), 6.75-6.84 (2H, m), 6.93-7.02 (2H, m), 7.18-7.28 (2H, m), 7.31-7.40 (2H, m), 7.45-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: the intermediate 426(2) and 4-(tert-butyl)phenylboronic acid; Yield: 24% (brown oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.14 (1H, s), 6.43-6.49 (1H, m), 6.71-6.77 (1H, m), 6.77-6.82 (1H, m), 6.95-7.04 (2H, m), 7.20-7.30 (2H, m), 7.32-7.41 (2H, m), 7.48-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 427(1) and ethyl bromoacetate; Yield: 65% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.29 (3H, t, J=7.2 Hz), 1.33 (9H, s), 4.27 (2H, q, J=7.2 Hz), 4.62 (2H, s), 6.51-6.56 (1H, m), 6.78-6.86 (2H, m), 6.94-7.02 (2H, m), 7.21-7.30 (2H, m), 7.32-7.40 (2H, m), 7.48-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 427(2); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.70 (2H, s), 6.52-6.59 (1H, m), 6.78-6.86 (2H, m), 6.94-7.03 (2H, m), 7.21-7.30 (2H, m), 7.32-7.42 (2H, m), 7.48-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 423(3) and 1-chlorobutane; Yield: 16% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.5 Hz), 1.23-1.47 (11H, m), 1.56-2.04 (2H, m), 3.20 (2H, t, J=6.6 Hz), 4.25 (1H, brs), 6.74-6.78 (1H, m), 6.84-6.88 (2H, m), 6.93-6.99 (2H, m), 7.24-7.27 (2H, m), 7.31-7.37 (2H, m), 7.55-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 428(1) and ethyl bromoacetate; Yield: 39% (colorless oil).
1H-NMR (CDCl3) δ: 0.84 (3H, t, J=7.5 Hz), 1.16 (3H, t, J=7.2 Hz), 1.16-1.26 (2H, m), 1.31 (9H, s), 1.43-1.54 (2H, m), 3.29-3.35 (2H, m), 4.02-4.10 (4H, m), 6.84-6.89 (2H, m), 6.95 (1H, d, J=8.4 Hz), 7.06 (1H, dd, J=2.1, 8.4 Hz), 7.23-7.33 (5H, m), 7.54-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 428(2); Yield: 42% (white solid).
1H-NMR (DMSO-d6) δ: 0.77 (3H, t, J=7.2 Hz), 1.05-1.17 (2H, m), 1.27 (9H, s), 1.35-1.48 (2H, m), 3.26-3.33 (2H, m), 4.00 (2H, s), 6.82-6.86 (2H, m), 6.92 (1H, d, J=8.1 Hz), 7.12-7.16 (1H, m), 7.22-7.24 (1H, m), 7.32-7.36 (2H, m), 7.42-7.46 (2H, m), 7.71-7.74 (2H, m), 12.33 (1H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 5-bromosalicylaldehyde and 1-bromohexane; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=7.0 Hz), 1.28-1.42 (4H, m), 1.42-1.54 (2H, m), 1.79-1.89 (2H, m), 4.06 (2H, t, J=6.4 Hz), 6.88 (1H, d, J=9.0 Hz), 7.60 (1H, dd, J=2.7, 8.9 Hz), 7.92 (1H, d, J=2.6 Hz), 10.42 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 429(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.0 Hz), 1.32-1.42 (4H, m), 1.45-1.57 (2H, m), 1.83-1.93 (2H, m), 4.13 (2H, t, J=6.4 Hz), 7.07 (1H, d, J=8.8 Hz), 7.25-7.30 (2H, m), 7.58 (2H, d, J=8.8 Hz), 7.74 (1H, dd, J=2.6, 8.6 Hz), 8.04 (1H, d, J=2.6 Hz), 10.55 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 429(2); Yield: 69% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.1 Hz), 1.32-1.42 (4H, m), 1.42-1.54 (2H, m), 1.78-1.89 (2H, m), 4.08 (2H, t, J=6.6 Hz), 5.71 (1H, s), 6.90 (1H, d, J=8.4 Hz), 7.03 (1H, dd, J=2.4, 8.4 Hz), 7.15 (1H, d, J=2.2 Hz), 7.22-7.27 (2H, m), 7.54 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 429(3) and ethyl 2-bromooctanoate; Yield: 77% (colorless oil).
1H-NMR (CDCl3) δ: 0.86-0.95 (6H, m), 1.24 (3H, t, J=7.1 Hz), 1.28-2.03 (14H, m), 3.97-4.07 (2H, m), 4.16-4.26 (2H, m), 4.68 (1H, t, J=6.3 Hz), 6.95 (1H, d, J=9.0 Hz), 7.13-7.18 (2H, m), 7.24 (2H, d, J=8.8 Hz), 7.50 (2H, d, J=8.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 429(4); Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 0.82-0.98 (6H, m), 1.25-1.69 (14H, m), 1.81-1.92 (2H, m), 2.00-2.09 (2H, m), 4.07 (2H, t, J=6.7 Hz), 4.62 (1H, t, J=5.7 Hz), 6.99 (1H, d, J=8.4 Hz), 7.17-7.30 (4H, m), 7.50 (2H, d, J=8.6 Hz).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-bromosalicylaldehyde and 1-bromohexane; Yield: 92% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.90-0.95 (3H, m), 1.33-1.39 (4H, m), 1.45-1.53 (2H, m), 1.82-1.91 (2H, m), 4.08 (2H, t, J=6.4 Hz), 7.16 (1H, s), 7.18-7.19 (1H, m), 7.70 (1H, dd, J=0.6, 7.9 Hz), 10.44 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 430(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 0.88-0.94 (3H, m), 1.33-1.40 (4H, m), 1.47-1.56 (2H, m), 1.84-1.93 (2H, m), 4.16 (2H, t, J=6.4 Hz), 7.11 (1H, d, J=1.3 Hz), 7.18-7.21 (1H, m), 7.30-7.34 (2H, m), 7.60-7.65 (2H, m), 7.91 (1H, d, J=7.9 Hz), 10.53 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 430(2); Yield: 81% (pink solid).
1H-NMR (CDCl3) δ: 0.90-0.94 (3H, m), 1.33-1.41 (4H, m), 1.44-1.53 (2H, m), 1.81-1.90 (2H, m), 4.11 (2H, t, J=6.6 Hz), 5.69 (1H, s), 6.98-7.08 (3H, m), 7.24-7.27 (2H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 430(3) and ethyl 2-bromooctanoate; Yield: 83% (colorless oil).
1H-NMR (CDCl3) δ: 0.87-0.94 (6H, m), 1.27 (3H, t, J=7.1 Hz), 1.27-1.38 (10H, m), 1.38-1.61 (4H, m), 1.79-2.05 (4H, m), 3.99-4.12 (2H, m), 4.17-4.28 (2H, m), 4.63-4.67 (1H, m), 6.94 (1H, d, J=8.2 Hz), 7.01-7.07 (2H, m), 7.24-7.27 (2H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 430(4); Yield: 87% (colorless solid).
1H-NMR (CDCl3) δ: 0.88-0.94 (6H, m), 1.24-1.52 (12H, m), 1.58-1.65 (2H, m), 1.83-1.93 (2H, m), 2.01-2.09 (2H, m), 4.08-4.12 (2H, m), 4.60 (1H, t, J=5.5 Hz), 7.04-7.11 (3H, m), 7.27-7.30 (2H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 2-fluoro-5-nitrobenzaldehyde and 4-(tert-butyl)phenol; Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 1.37 (9H, s), 6.93 (1H, d, J=9.0 Hz), 7.06-7.16 (2H, m), 7.47-7.52 (2H, m), 8.30 (1H, dd, J=3.0, 9.0 Hz), 8.79 (1H, d, J=3.0 Hz), 10.60 (1H, s).
A mixture of the intermediate 431(1) (620 mg, 2.07 mmol), ethylene glycol (141 mg, 2.27 mmol), p-toluenesulfonic acid monohydrate (5 mg) and toluene (5 ml) was refluxed for 5 hours. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (730 mg, 100%) as a yellow oil
1H-NMR (CDCl3) δ: 1.34 (9H, s), 4.08-4.10 (2H, m), 4.20-4.22 (2H, m), 6.26 (1H, s), 6.83 (1H, d, J=9.0 Hz), 7.00-7.04 (2H, m), 7.41-7.44 (2H, m), 8.12 (1H, dd, J=2.7, 9.0 Hz), 8.52 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 431(2); Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.62 (2H, brs), 3.96-3.99 (2H, m), 4.10-4.12 (2H, m), 5.99 (1H, s), 6.64 (1H, dd, J=3.0, 9.0 Hz), 6.78 (1H, d, J=9.0 Hz), 6.84-6.88 (2H, m), 6.95 (1H, d, J=3.0 Hz), 7.26-7.29 (2H, m).
The title compound was obtained in the same manner as the Example 412(1) using the following starting materials.
Starting materials: the intermediate 431(3) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 24% (brown oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.97-4.00 (2H, m), 4.10-4.13 (2H, m), 5.68 (1H, s), 6.08 (1H, s), 6.86 (1H, d, J=9.0 Hz), 6.91-6.96 (4H, m), 7.03-7.12 (3H, m), 7.30-7.34 (3H, m).
A mixture of the intermediate 431(4) (220 mg, 0.465 mmol), pyridinium p-toluenesulfonate (35 mg, 0.139 mmol), acetone (10 ml) and water (2 ml) was stirred at 70° C. for 1 hour. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with n-hexane to give the title compound (155 mg, 77%) as a yellow solid.
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.72 (1H, s), 6.91-7.01 (5H, m), 7.11-7.14 (2H, m), 7.23-7.26 (1H, m), 7.36-7.39 (2H, m), 7.59 (1H, d, J=3.0 Hz), 10.42 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 431(5) and malonic acid; Yield: 91% (yellow solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 6.49 (1H, d, J=15.9 Hz), 6.87 (1H, d, J=8.7 Hz), 6.90-6.93 (2H, m), 6.96-6.99 (2H, m), 7.05 (1H, dd, J=2.7, 8.7 Hz), 7.11-7.15 (2H, m), 7.33-7.36 (3H, m), 8.02 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 431; Yield: 83% (whitish-pink solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.19 (2H, t, J=7.2 Hz), 2.65 (2H, t, J=7.2 Hz), 6.76-6.80 (3H, m), 6.92 (1H, dd, J=2.7, 8.7 Hz), 7.05-7.09 (3H, m), 7.16-7.19 (2H, m), 7.30-7.35 (2H, m), 8.28 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-bromo-2-nitrophenol and 4-phenylbutyl bromide; Yield: 82% (yellow oil).
1H-NMR (CDCl3) δ: 1.73-1.95 (4H, m), 2.61-2.77 (2H, m), 4.02-4.12 (2H, m), 6.92 (1H, d, J=9.0 Hz), 7.12-7.24 (3H, m), 7.23-7.36 (2H, m), 7.59 (1H, dd, J=2.4, 9.0 Hz), 7.95 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 433(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 86% (yellow oil).
1H-NMR (CDCl3) δ: 1.78-1.98 (4H, m), 2.63-2.78 (2H, m), 4.10-4.20 (2H, m), 7.11 (1H, d, J=8.7 Hz), 7.15-7.25 (3H, m), 7.25-7.38 (4H, m), 7.51-7.62 (2H, m), 7.68 (1H, dd, J=2.4, 8.7 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 433(2); Yield: 97% (green oil).
1H-NMR (CDCl3) δ: 1.72-1.96 (4H, m), 2.62-2.77 (2H, m), 3.69 (2H, brs), 3.94-4.10 (2H, m), 6.76-6.84 (1H, m), 6.84-6.94 (2H, m), 7.14-7.35 (7H, m), 7.44-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 433(3) and 1-iodobutane; Yield: 38% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.36-1.56 (2H, m), 1.59-1.73 (2H, m), 1.74-1.95 (4H, m), 2.70 (2H, t, J=6.9 Hz), 3.18 (2H, t, J=6.9 Hz), 4.03 (2H, d, J=6.0 Hz), 4.24 (1H, brs), 6.72-6.84 (3H, m), 7.14-7.36 (7H, m), 7.50-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 433(4) and ethyl bromoacetate; Yield: 63% (pale yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.2 Hz), 1.10-1.45 (5H, m), 1.45-1.70 (2H, m), 1.74-1.97 (4H, m), 2.62-2.78 (2H, m), 3.23-3.38 (2H, m), 3.95-4.18 (6H, m), 6.80-6.92 (2H, m), 7.04-7.13 (1H, m), 7.08 (1H, dd, J=2.4, 8.4 Hz), 7.13-7.37 (6H, m), 7.46-7.60 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.2 Hz), 1.10-1.45 (5H, m), 1.45-1.70 (2H, m), 1.74-1.97 (4H, m), 2.62-2.78 (2H, m), 3.23-3.38 (2H, m), 3.95-4.32 (6H, m), 6.80-6.92 (2H, m), 7.04-7.13 (1H, m), 7.08 (1H, dd, J=2.4, 8.4 Hz), 7.13-7.37 (6H, m), 7.46-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 433(5); Yield: 36% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.21-1.42 (2H, m), 1.42-1.58 (2H, m), 1.72-2.00 (4H, m), 2.71 (2H, t, J=7.5 Hz), 3.12 (2H, t, J=7.5 Hz), 3.66 (2H, s), 4.06 (2H, t, J=6.6 Hz), 6.91-6.99 (1H, m), 7.14-7.36 (9H, m), 7.46-7.57 (2H, m).
A mixture of the intermediate 110(1) (118 mg, 0.285 mmol), sodium chlorite (38.0 mg, 0.427 mmol), acetonitrile (3 ml) and water (0.3 ml) was stirred at room temperature for 18 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (45.0 mg, 37%) as a white solid.
1H-NMR (CDCl3) δ: 1.35 (9H, s), 7.02 (1H, d, J=2.1 Hz), 7.07-7.14 (2H, m), 7.22-7.30 (2H, m), 7.39 (1H, dd, J=2.1, 8.1 Hz), 7.42-7.52 (4H, m), 8.30 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 423(3) and 1-iodopropane; Yield: 63% (brown oil).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.5 Hz), 1.32 (9H, s), 1.58-1.76 (2H, m), 3.04-3.28 (2H, m), 4.29 (1H, brs), 6.76 (1H, dd, J=2.1, 8.1 Hz), 6.82-6.91 (2H, m), 6.92-7.01 (2H, m), 7.20-7.30 (2H, m), 7.30-7.40 (2H, m), 7.52-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 435(1) and ethyl bromoacetate; Yield: 15% (brown oil).
1H-NMR (CDCl3) δ: 0.77 (3H, t, J=7.2 Hz), 1.15 (3H, t, J=7.2 Hz), 1.31 (9H, s), 1.44-1.62 (2H, m), 3.20-3.35 (2H, m), 3.96-4.16 (4H, m), 6.81-6.92 (2H, m), 6.95 (1H, d, J=8.4 Hz), 7.05 (1H, dd, J=2.1, 8.4 Hz), 7.21-7.35 (5H, m), 7.51-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 435(2); Yield: 100% (brown oil).
1H-NMR (CDCl3) δ: 0.70-0.86 (3H, m), 1.29 (9H, s), 1.38-1.56 (2H, m), 2.96-3.15 (2H, m), 3.75 (2H, s), 6.80-6.98 (3H, m), 7.05-7.16 (1H, m), 7.19-7.40 (5H, m), 7.44-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 335(1); Yield: 86% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 5.68 (1H, s), 6.83-6.85 (1H, m), 7.10-7.32 (8H, m), 7.44-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 436(1) and ethyl bromoacetate; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.0 Hz), 1.31 (9H, s), 4.24 (2H, q, J=7.0 Hz), 4.73 (2H, s), 6.75-6.79 (1H, m), 7.02 (1H, d, J=8.6 Hz), 7.10-7.28 (7H, m), 7.45-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 436(2); Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.74 (2H, s), 6.76-6.79 (1H, m), 7.07 (1H, d, J=8.4 Hz), 7.13-7.56 (2H, m), 7.20-7.30 (5H, m), 7.45-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and 3-(tert-butyl)phenol; Yield: 96% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.89-6.92 (1H, m), 6.97 (1H, d, J=8.6 Hz), 7.18-7.19 (1H, m), 7.24-7.38 (4H, m), 7.58-7.63 (2H, m), 7.69 (1H, dd, J=2.6, 8.6 Hz), 8.14 (1H, d, J=2.2 Hz), 10.61 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 437(2) and malonic acid; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 6.67 (1H, d, J=16.2 Hz), 6.80-6.85 (1H, m), 6.91 (1H, d, J=8.6 Hz), 7.13-7.15 (1H, m), 7.22-7.34 (4H, m), 7.48 (1H, dd, J=2.2, 8.6 Hz), 7.56-7.60 (2H, m), 7.80 (1H, d, J=2.2 Hz), 8.19 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 437; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.77 (2H, t, J=7.7 Hz), 3.08 (2H, t, J=7.7 Hz), 6.75-6.79 (1H, m), 6.88 (1H, d, J=8.4 Hz), 7.09-7.10 (1H, m), 7.14-7.17 (1H, m), 7.24-7.29 (3H, m), 7.34 (1H, dd, J=2.2, 8.4 Hz), 7.47 (1H, d, J=2.2 Hz), 7.53-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 437(1); Yield: 94% (yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.70 (1H, s), 6.83-6.86 (1H, m), 6.92 (1H, d, J=8.4 Hz), 7.02 (1H, dd, J=2.2, 8.2 Hz), 7.15-7.16 (1H, m), 7.18-7.21 (1H, m), 7.25-7.32 (4H, m), 7.55-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 439(1) and ethyl bromoacetate; Yield: 86% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.1 Hz), 1.32 (9H, s), 4.24 (2H, q, J=7.1 Hz), 4.75 (2H, s), 6.77-6.81 (1H, m), 7.00 (1H, d, J=8.6 Hz), 7.11-7.17 (4H, m), 7.22-7.30 (3H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 439(2); Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 4.77 (2H, s), 6.77-6.81 (1H, m), 7.02-7.05 (1H, m), 7.13-7.23 (7H, m), 7.53-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(pentyloxy)phenylboronic acid; Yield: 86% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.33-1.51 (4H, m), 1.73-1.85 (2H, m), 3.96 (2H, t, J=6.6 Hz), 4.22 (2H, q, J=7.2 Hz), 4.69 (2H, s), 6.87-6.98 (4H, m), 7.01 (1H, d, J=8.4 Hz), 7.18 (1H, d, J=2.4 Hz), 7.25 (1H, dd, J=2.4, 8.4 Hz), 7.27-7.34 (2H, m), 7.36-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 440(1); Yield: 56% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.31 (9H, s), 1.33-1.50 (4H, m), 1.73-1.85 (2H, m), 3.97 (2H, t, J=6.6 Hz), 4.69 (2H, s), 6.90-6.99 (4H, m), 7.06 (1H, d, J=8.4 Hz), 7.21 (1H, d, J=2.4 Hz), 7.29 (1H, dd, J=2.4, 8.4 Hz), 7.31-7.38 (2H, m), 7.37-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(isopropyl)phenylboronic acid; Yield: 52% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (6H, d, J=6.9 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 2.91 (1H, sept, J=6.9 Hz), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.87-6.98 (2H, m), 7.01 (1H, d, J=8.4 Hz), 7.16-7.34 (6H, m), 7.35-7.45 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 441(1); Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=6.9 Hz), 1.30 (9H, s), 2.92 (1H, sept, J=6.9 Hz), 4.73 (2H, s), 6.90-7.00 (2H, m), 7.05 (1H, d, J=8.4 Hz), 7.20-7.29 (4H, m), 7.29-7.36 (2H, m), 7.36-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 4-bromo-2-fluoro-1-nitrobenzene and 4-(trifluoromethoxy)phenylboronic acid; Yield: 91% (yellow solid).
1H-NMR (CDCl3) δ: 7.31-7.41 (2H, m), 7.43-7.53 (2H, m), 7.58-7.68 (2H, m), 8.18 (1H, t, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 442(1) and 4-(tert-butyl)phenol; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 6.98-7.06 (2H, m), 7.18 (1H, d, J=2.1 Hz), 7.24-7.32 (2H, m), 7.34 (1H, dd, J=2.1, 8.4 Hz), 7.37-7.44 (2H, m), 7.46-7.55 (2H, m), 8.05 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 442(2); Yield: 92% (brown oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.91 (2H, brs), 6.88 (1H, d, J=8.1 Hz), 6.91-6.98 (2H, m), 7.11 (1H, d, J=1.8 Hz), 7.16-7.25 (3H, m), 7.30-7.38 (2H, m), 7.44-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 442(3) and ethyl bromoacetate; Yield: 33% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.20-1.38 (12H, m), 3.98 (2H, d, J=5.4 Hz), 4.23 (2H, q, J=7.2 Hz), 4.86-4.98 (1H, m), 6.67 (1H, d, J=8.4 Hz), 6.93-7.02 (2H, m), 7.09 (1H, d, J=2.1 Hz), 7.14-7.28 (3H, m), 7.29-7.38 (2H, m), 7.41-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 442(4); Yield: 87% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 3.91 (2H, s), 5.58 (1H, brs), 6.72 (1H, d, J=8.4 Hz), 6.85-6.96 (2H, m), 7.16 (1H, d, J=1.8 Hz), 7.26-7.43 (5H, m), 7.58-7.69 (2H, m), 12.70 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-butylphenylboronic acid; Yield: 89% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.31-1.34 (2H, m), 1.54-1.65 (2H, m), 2.61 (2H, t, J=7.5 Hz), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.93-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.18-7.22 (3H, m), 7.27-7.34 (3H, m), 7.37-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 443(1); Yield: 82% (white solid).
1H-NMR (DMSO-d6) δ: 0.989 (3H, t, J=6.9 Hz), 1.26 (9H, s), 1.29-1.36 (2H, m), 1.50-1.60 (2H, m), 2.58 (2H, t, J=7.5 Hz), 4.74 (2H, s), 6.87 (2H, d, J=8.7 Hz), 7.10 (1H, d, J=8.7 Hz), 7.22 (2H, d, J=8.1 Hz), 7.26 (1H, d, J=2.1 Hz), 7.33 (2H, d, J=8.7 Hz), 7.43 (1H, dd, J=2.1, 8.7 Hz), 7.48 (2H, d, J=8.7 Hz), 13.06 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-methyphenylboronic acid; Yield: 57% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 2.36 (3H, s), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.92-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.18-7.22 (3H, m), 7.25-7.39 (5H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 444(1); Yield: 83% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.31 (3H, s), 4.74 (2H, s), 6.85-6.89 (2H, m), 7.11 (1H, d, J=8.7 Hz), 7.21 (2H, d, J=8.1 Hz), 7.27 (1H, d, J=2.4 Hz), 7.30-7.34 (2H, m), 7.41-67.49 (3H, m), 13.03 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-methoxyphenylboronic acid; Yield: 80% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 3.82 (3H, s), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.89-6.98 (4H, m), 7.01 (1H, d, J=8.1 Hz), 7.19 (1H, d, J=2.1 Hz), 7.25 (1H, dd, J=2.1, 8.1 Hz), 7.29-7.34 (2H, m), 7.39-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 445(1); Yield: 89% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 3.76 (3H, s), 4.73 (2H, s), 6.86 (2H, d, J=8.4 Hz), 6.96 (2H, d, J=8.7 Hz), 7.09 (1H, d, J=8.4 Hz), 7.24 (1H, d, J=2.4 Hz), 7.33 (2H, d, J=8.7 Hz), 7.39 (1H, dd, J=2.4, 8.7 Hz), 7.52 (2H, d, J=8.7 Hz), 13.03 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(tert-butyl)phenylboronic acid; Yield: 66% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.32 (9H, s), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.91-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.22 (1H, d, J=2.4 Hz), 7.23-7.34 (3H, m), 7.35-7.44 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 446(1); Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 1.34 (9H, s), 4.71 (2H, s), 6.92-7.00 (2H, m), 7.07 (1H, d, J=8.4 Hz), 7.24 (1H, d, J=2.4 Hz), 7.29-7.38 (3H, m), 7.40-7.44 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: 4-bromophenol and 3-bromopentane; Yield: 71% (colorless oil).
1H-NMR (CDCl3) δ: 0.94 (6H, t, J=7.5 Hz), 1.60-1.73 (4H, m), 4.06 (1H, quint, J=6.0 Hz), 6.73-6.82 (2H, m), 7.31-7.38 (2H, m).
A 1.6 M solution of n-Butyllithium in hexane (1.91 ml, 3.05 mmol) was added dropwise to a solution of the intermediate 447(1) (742 mg, 3.05 mmol) in anhydrous tetrahydrofuran (10 ml) at −78° C. After the reaction mixture was allowed to warm to −30° C., triisopropyl borate (0.73 ml, 3.20 mmol) was added to the reaction mixture, followed by stirring at room temperature for 1 hour. 2 N hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (381 mg, 60%) as a white solid.
1H-NMR (CDCl3) δ: 0.99 (6H, t, J=7.5 Hz), 1.63-1.79 (4H, m), 4.25 (1H, quint, J=6.0 Hz), 6.95-7.04 (2H, m), 8.11-8.18 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediates 315 (2) and 447 (2); Yield: 81% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (6H, t, J=7.5 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.61-1.74 (4H, m), 4.11 (1H, quint, J=5.7 Hz), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.96-6.99 (4H, m), 7.01 (1H, d, J=8.4 Hz), 7.18 (1H, d, J=2.4 Hz), 7.24 (1H, dd, J=2.4, 8.4 Hz), 7.28-7.35 (2H, m), 7.35-7.42 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 447(3); Yield: 80% (white solid).
1H-NMR (CDCl3) δ: 0.96 (6H, t, J=7.5 Hz), 1.31 (9H, s), 1.61-1.74 (4H, m), 4.12 (1H, quint, J=5.7 Hz), 4.69 (2H, s), 6.89-6.99 (4H, m), 7.06 (1H, d, J=8.4 Hz), 7.20 (1H, d, J=2.4 Hz), 7.27 (1H, dd, J=2.4, 8.4 Hz), 7.32-7.36 (2H, m), 7.36-7.42 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(methylthio)phenylboronic acid; Yield: 94% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 2.49 (3H, s), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.91-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.21 (1H, d, J=2.4 Hz), 7.23-7.35 (5H, m), 7.36-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 448(1); Yield: 79% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.50 (3H, s), 4.71 (2H, s), 6.92-6.98 (2H, m), 7.07 (1H, d, J=8.4 Hz), 7.22 (1H, d, J=2.4 Hz), 7.24-7.38 (5H, m), 7.37-7.45 (2H, m).
A mixture of the intermediate 448(1) (206 mg, 0.457 mmol), m-chloroperbenzoic acid (819 mg, 2.29 mmol) and chloroform (5 ml) was stirred at room temperature for 1 hour. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (195 mg, 88%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.30 (9H, s), 3.06 (3H, s), 4.24 (2H, q, J=7.2 Hz), 4.74 (2H, s), 6.91-7.00 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.25 (1H, d, J=2.4 Hz), 7.30-7.38 (3H, m), 7.63-7.69 (2H, m), 7.92-7.99 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 449(1); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.07 (3H, s), 4.75 (2H, s), 6.92-7.00 (2H, m), 7.11 (1H, d, J=8.4 Hz), 7.26 (1H, d, J=2.4 Hz), 7.32-7.40 (3H, m), 7.64-7.70 (2H, m), 7.93-8.00 (2H, m).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 110(1) and bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate; Yield: 50% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.72 (3H, s), 6.01 (1H, d, J=12.3 Hz), 6.90-6.97 (2H, m), 6.97-7.11 (1H, m), 7.20-7.27 (2H, m), 7.30-7.37 (4H, m), 7.49-7.57 (2H, m), 7.81 (1H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 450(1); Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 6.03 (1H, d, J=12.3 Hz), 6.91-6.98 (2H, m), 7.07 (1H, d, J=1.8 Hz), 7.20-7.39 (6H, m), 7.46-7.55 (2H, m), 7.80 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 308(1) and ethyl bromoacetate; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.33 (9H, s), 4.20 (2H, q, J=7.2 Hz), 4.66 (2H, s), 5.10 (2H, s), 6.55-6.64 (2H, m), 6.90-6.97 (3H, m), 7.11-7.18 (2H, m), 7.38-7.42 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 451(1); Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.66 (2H, s), 5.10 (2H, s), 6.64-6.74 (2H, m), 6.92-6.99 (3H, m), 7.12-7.19 (2H, m), 7.32-7.46 (4H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 309(2) and ethyl bromoacetate; Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.75-1.94 (4H, m), 2.70 (2H, t, J=7.2 Hz), 4.02 (2H, t, J=6.0 Hz), 4.20 (2H, q, J=7.2 Hz), 4.63 (2H, s), 6.55-6.65 (2H, m), 6.85 (1H, d, J=8.1 Hz), 6.89-6.97 (2H, m), 7.10-7.34 (7H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 452(1); Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 1.73-1.95 (4H, m), 2.70 (2H, t, J=7.2 Hz), 4.04 (2H, t, J=6.0 Hz), 4.64 (2H, s), 6.55-6.64 (2H, m), 6.85-6.98 (3H, m), 7.12-7.34 (7H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 5-bromo-2-fluorobenzaldehyde and 4-(tert-butyl)phenol; Yield: 90% (pale brown solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 6.79 (1H, d, J=8.8 Hz), 6.97-7.02 (2H, m), 7.39-7.44 (2H, m), 7.56 (1H, dd, J=2.6, 8.8 Hz), 8.02 (1H, d, J=2.6 Hz), 10.45 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 453(1); Yield: 69% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 5.63 (1H, s), 6.71 (1H, d, J=8.6 Hz), 6.88-6.95 (3H, m), 7.17 (1H, d, J=2.2 Hz), 7.31-7.36 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 453(2) and ethyl bromoacetate; Yield: 94% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 1.31 (9H, s), 4.23 (2H, q, J=7.1 Hz), 4.66 (2H, s), 6.82-6.85 (1H, m), 6.88-6.93 (2H, m), 7.06-7.10 (2H, m), 7.29-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 453(3) and 4-(tert-butyl)phenylboronic acid; Yield: 26% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.0 Hz), 1.31 (9H, s), 1.36 (9H, s), 4.22 (2H, q, J=7.0 Hz), 4.73 (2H, s), 6.93-7.02 (3H, m), 7.16-7.19 (2H, m), 7.30-7.35 (2H, m), 7.43-7.50 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 453(4); Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.36 (9H, s), 4.73 (2H, s), 6.94-6.99 (2H, m), 7.05 (1H, d, J=8.2 Hz), 7.22-7.26 (2H, m), 7.33-7.39 (2H, m), 7.48 (4H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 453(3) and 4-(n-pentyloxy)phenylboronic acid; Yield: 78% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.1 Hz), 1.25 (3H, t, J=7.1 Hz), 1.31 (9H, s), 1.34-1.52 (4H, m), 1.77-1.86 (2H, m), 4.00 (2H, t, J=6.4 Hz), 4.22 (2H, q, J=7.1 Hz), 4.73 (2H, s), 6.92-7.02 (5H, m), 7.13-7.16 (2H, m), 7.30-7.35 (2H, m), 7.43-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 454(1); Yield: 68% (white solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.0 Hz), 1.31 (9H, s), 1.32-1.52 (4H, m), 1.77-1.86 (2H, m), 4.00 (2H, t, J=6.6 Hz), 4.73 (2H, s), 6.93-6.99 (4H, m), 7.02-7.05 (1H, m), 7.18-7.22 (2H, m), 7.32-7.37 (2H, m), 7.43-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 2,5-dichlorophenylboronic acid; Yield: 82% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.30 (9H, s), 4.24 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.94-6.98 (2H, m), 7.00 (1H, d, J=8.4 Hz), 7.08 (1H, d, J=2.1 Hz), 7.12 (1H, dd, J=2.1, 8.4 Hz), 7.21 (1H, dd, J=2.4, 8.4 Hz), 7.29 (1H, d, J=2.4 Hz), 7.31-7.38 (2H, m), 7.35 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 455(1); Yield: 61% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.79 (2H, s), 6.86-6.92 (2H, m), 7.09 (1H, d, J=2.1 Hz), 7.12 (1H, d, J=8.4 Hz), 7.23 (1H, dd, J=2.1, 8.4 Hz), 7.32-7.38 (2H, m), 7.44 (1H, dd, J=2.7, 8.4 Hz), 7.48 (1H, d, J=2.7 Hz), 7.56 (1H, d, J=8.4 Hz), 13.01 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 2-(trifluoromethoxy)phenylboronic acid; Yield: 77% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 4.24 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.93-6.98 (2H, m), 7.01 (1H, d, J=8.4 Hz), 7.11 (1H, d, J=2.1 Hz), 7.15 (1H, dd, J=2.1, 8.4 Hz), 7.28-7.38 (6H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 456(1); Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.77 (2H, s), 6.85-6.90 (2H, m), 7.07 (1H, d, J=2.1 Hz), 7.13 (1H, d, J=8.4 Hz), 7.23 (1H, dd, J=2.1, 8.4 Hz), 7.31-7.40 (2H, m), 7.43-7.53 (4H, m), 13.12 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-chlorophenylboronic acid; Yield: 77% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.92-6.97 (2H, m), 7.02 (1H, d, J=8.7 Hz), 7.19 (1H, d, J=2.4 Hz), 7.26 (1H, dd, J=2.4, 8.7 Hz), 7.29-7.42 (6H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 457(1); Yield: 86% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.76 (2H, s), 6.85-6.89 (2H, m), 7.13 (1H, d, J=8.7 Hz), 7.30-7.34 (3H, m), 7.44-7.50 (3H, m), 7.61-7.66 (2H, m), 13.05 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and phenylboronic acid; Yield: 52% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.93-6.98 (2H, m), 7.03 (1H, d, J=8.7 Hz), 7.24 (1H, d, J=2.1 Hz), 7.29-7.41 (6H, m), 7.46-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 458(1); Yield: 94% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.76 (2H, s), 6.87 (2H, d, J=9.0 Hz), 7.13 (1H, d, J=8.7 Hz), 7.30-7.48 (7H, m), 7.58 (2H, d, J=7.5 Hz), 13.04 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-fluorophenylboronic acid; Yield: 76% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.93-6.97 (2H, m), 7.02 (1H, d, J=8.7 Hz), 7.04-7.10 (2H, m), 7.18 (1H, d, J=2.4 Hz), 7.23 (1H, dd, J=2.4, 8.7 Hz), 7.29-7.35 (2H, m), 7.41-7.45 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 459(1); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.76 (2H, s), 6.87 (2H, d, J=9.0 Hz), 7.12 (1H, d, J=8.7 Hz), 7.20-7.26 (2H, m), 7.30 (1H, d, J=2.4 Hz), 7.33 (2H, d, J=9.0 Hz), 7.45 (1H, dd, J=2.4, 8.7 Hz), 7.61-7.65 (2H, m), 13.05 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(isopropoxy)phenylboronic acid; Yield: 60% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.34 (6H, d, J=6.0 Hz), 4.22 (2H, q, J=7.2 Hz), 4.55 (1H, sept, J=6.0 Hz), 4.70 (2H, s), 6.87-6.92 (2H, m), 6.93-6.97 (2H, m), 7.01 (1H, d, J=8.4 Hz), 7.19 (1H, d, J=2.4 Hz), 7.24 (1H, dd, J=2.4, 8.4 Hz), 7.29-7.34 (2H, m), 7.37-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 460(1); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 1.256 (9H, s), 1.261 (6H, d, J=6.0 Hz), 4.62 (1H, sept, J=6.0 Hz), 4.74 (2H, s), 6.84-6.89 (2H, m), 6.92-6.96 (2H, m), 7.09 (1H, d, J=8.7 Hz), 7.23 (1H, d, J=2.4 Hz), 7.30-7.35 (2H, m), 7.39 (1H, dd, J=2.4, 8.7 Hz), 7.45-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and p-butoxyphenol; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.2 Hz), 1.50-1.57 (2H, m), 1.75-1.83 (2H, m), 3.97 (2H, t, J=6.6 Hz), 6.92-6.95 (3H, m), 7.05-7.08 (2H, m), 7.23-7.27 (2H, m), 7.29-7.33 (1H, m), 7.47-7.50 (2H, m), 7.99 (1H, d, J=8.1 Hz), 10.59 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 461(1) and malonic acid; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.2 Hz), 1.47-1.55 (2H, m), 1.75-1.83 (2H, m), 3.96 (2H, t, J=6.6 Hz), 6.64 (1H, d, J=16.2 Hz), 6.89-7.02 (5H, m), 7.22-7.28 (3H, m), 7.45-7.50 (2H, m), 7.69 (1H, d, J=8.4 Hz), 8.18 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 461(2); Yield: 34% (white solid).
1H-NMR (DMSO-d6) δ: 0.93 (3H, t, J=7.2 Hz), 1.39-1.46 (2H, m), 1.63-1.73 (2H, m), 2.57 (2H, t, J=7.5 Hz), 2.88 (2H, t, J=7.5 Hz), 3.93 (2H, t, J=6.6 Hz), 6.92-6.99 (5H, m), 7.34-7.42 (4H, m), 7.62-7.65 (2H, m), 12.17 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-(tert-butyl)thiophenol; Yield: 93% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.20-7.29 (3H, m), 7.36-7.46 (6H, m), 7.49 (1H, dd, J=1.8, 8.1 Hz), 7.94 (1H, d, J=8.1 Hz), 10.42 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 462(1) and malonic acid; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 6.43 (1H, d, J=15.9 Hz), 7.22-7.41 (6H, m), 7.46-7.55 (4H, m), 7.73 (1H, d, J=8.1 Hz), 8.42 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and phenol; Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 7.01 (1H, d, J=1.8 Hz), 7.06-7.14 (2H, m), 7.21-7.29 (1H, m), 7.31 (1H, ddd, J=1.2, 2.1, 8.4 Hz), 7.40-7.48 (2H, m), 7.79 (1H, d, J=8.4 Hz), 10.48 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 463(1) and phenylboronic acid; Yield: 95% (pale yellow solid).
1H-NMR (CDCl3) δ: 7.08-7.15 (3H, m), 7.15-7.24 (1H, m), 7.42-7.55 (8H, m), 8.01 (1H, d, J=8.1 Hz), 10.53 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 463(2) and malonic acid; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 6.61 (1H, d, J=16.2 Hz), 7.02-7.19 (4H, m), 7.29-7.45 (6H, m), 7.47-7.54 (2H, m), 7.73 (1H, d, J=8.1 Hz), 8.13 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 463; Yield: 50% (white solid).
1H-NMR (CDCl3) δ: 2.73 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 6.96-7.03 (2H, m), 7.04-7.13 (2H, m), 7.27-7.43 (7H, m), 7.44-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 3-(tert-butyl)phenol; Yield: 87% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.87 (1H, ddd, J=1.2, 2.4, 7.8 Hz), 7.01 (1H, d, J=1.8 Hz), 7.14 (1H, t, J=2.4 Hz), 7.25-7.40 (3H, m), 7.79 (1H, d, J=8.4 Hz), 10.50 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 465(1) and 4-(tert-butyl)phenylboronic acid; Yield: 98% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.34 (9H, s), 6.88 (1H, ddd, J=1.2, 2.4, 7.8 Hz), 7.10 (1H, d, J=1.8 Hz), 7.16-7.36 (3H, m), 7.36-7.48 (5H, m), 7.99 (1H, d, J=8.4 Hz), 10.54 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 465(2); Yield: 94% (pale brown oil).
1H-NMR (CDCl3) δ: 1.32 (18H, s), 5.61 (1H, s), 6.77-6.91 (2H, m), 7.07-7.19 (3H, m), 7.20-7.31 (3H, m), 7.32-7.42 (3H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 465(3) and ethyl bromoacetate; Yield: 38% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.31 (9H, s), 1.33 (9H, s), 4.22 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.77 (1H, ddd, J=0.9, 2.7, 8.1 Hz), 7.01 (1H, d, J=8.4 Hz), 7.07-7.13 (1H, m), 7.13-7.17 (1H, m), 7.18-7.25 (2H, m), 7.29 (1H, dd, J=2.1, 8.4 Hz), 7.38-7.43 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 465(4); Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 1.34 (9H, s), 4.71 (2H, s), 6.77 (1H, ddd, J=0.9, 2.7, 8.1 Hz), 7.06 (1H, d, J=8.4 Hz), 7.11-7.19 (2H, m), 7.20-7.29 (2H, m), 7.33 (1H, dd, J=2.1, 8.4 Hz), 7.40-7.44 (4H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 2-(trifluoromethoxy)phenylboronic acid; Yield: 94% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.02-7.07 (3H, m), 7.24-7.27 (1H, m), 7.31-7.44 (6H, m), 8.00 (1H, d, J=8.1 Hz), 10.58 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 466(1) and malonic acid; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.65 (1H, d, J=16.2 Hz), 6.97-7.03 (3H, m), 7.22 (1H, dd, J=1.5, 8.1 Hz), 7.29-7.42 (6H, m), 7.72 (1H, d, J=8.1 Hz), 8.17 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 466; Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.76 (2H, t, J=7.3 Hz), 3.05 (2H, t, J=7.3 Hz), 6.91-6.93 (2H, m), 6.99 (1H, d, J=1.7 Hz), 7.15 (1H, dd, J=1.7, 7.7 Hz), 7.28-7.38 (7H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-hydroxyphenylboronic acid; Yield: 56% (white solid).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.70 (2H, s), 5.22 (1H, brs), 6.81-6.86 (2H, m), 6.92-6.97 (2H, m), 7.00 (1H, d, J=8.4 Hz), 7.17 (1H, d, J=2.1 Hz), 7.21 (1H, dd, J=2.1, 8.4 Hz), 7.28-7.36 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 468(1) and 1-iodobutane; Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.26 (3H, t, J=7.2 Hz), 1.30 (9H, s), 1.43-1.55 (2H, m), 1.72-1.82 (2H, m), 3.97 (2H, t, J=6.6 Hz), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.88-6.97 (4H, m), 7.01 (1H, d, J=8.7 Hz), 7.19 (1H, d, J=2.1 Hz), 7.25 (1H, dd, J=2.1, 8.7 Hz), 7.29-7.34 (2H, m), 7.37-7.42 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 468(2); Yield: 84% (white solid).
1H-NMR (DMSO-d6) δ: 0.93 (3H, t, J=7.5 Hz), 1.26 (9H, s), 1.43 (2H, sext, J=7.5 Hz), 1.72 (2H, quint, J=6.6 Hz), 3.97 (2H, t, J=6.6 Hz), 4.73 (2H, s), 6.85-6.89 (2H, m), 6.93-6.97 (2H, m), 7.09 (1H, d, J=8.4 Hz), 7.23 (1H, d, J=2.1 Hz), 7.30-7.35 (2H, m), 7.39 (1H, dd, J=2.1, 8.4 Hz), 7.48-7.51 (2H, m), 13.03 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 2-naphthaleneboronic acid; Yield: 92% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.04-7.09 (2H, m), 7.27 (1H, d, J=1.8 Hz), 7.39-7.44 (2H, m), 7.48-7.56 (3H, m), 7.63 (1H, dd, J=1.8, 8.4 Hz), 7.82-7.91 (3H, m), 7.98 (1H, d, J=4.8 Hz), 8.05 (1H, d, J=8.1 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 469(1) and malonic acid; Yield: 96% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 6.69 (1H, d, J=16.2 Hz), 6.94-6.98 (2H, m), 7.39-7.43 (3H, m), 7.51-7.57 (2H, m), 7.72-7.83 (3H, m), 7.97-8.01 (3H, m), 8.07 (1H, d, J=8.1 Hz), 8.26 (1H, s), 12.51 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 469; Yield: 89% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.57 (2H, t, J=7.8 Hz), 2.85 (2H, t, J=7.8 Hz), 6.90-6.93 (2H, m), 7.32 (1H, d, J=1.8 Hz), 7.37-7.40 (2H, m), 7.48-7.55 (3H, m), 7.56 (1H, dd, J=1.8, 8.1 Hz), 7.75 (1H, dd, J=1.8, 8.4 Hz), 7.90-7.98 (3H, m), 8.16 (1H, s), 12.24 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-cyanophenylboronic acid; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.24 (2H, q, J=7.2 Hz), 4.74 (2H, s), 6.93-6.98 (2H, m), 7.4 (1H, d, J=8.7 Hz), 7.24 (1H, d, J=2.4 Hz), 7.30-7.36 (3H, m), 7.56-7.58 (2H, m), 7.66-7.68 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 471(1); Yield: 77% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 4.79 (2H, s), 6.85-6.90 (2H, m), 7.17 (1H, d, J=8.4 Hz), 7.31-7.34 (2H, m), 7.45 (1H, d, J=2.4 Hz), 7.59 (1H, dd, J=2.4, 8.4 Hz), 7.81-7.88 (4H, m), 13.12 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and m-butoxyphenol; Yield: 72% (yellow oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.2 Hz), 1.44-1.54 (2H, m), 1.72-1.80 (2H, m), 3.95 (2H, t, J=6.6 Hz), 6.65-6.75 (3H, m), 7.11 (1H, d, J=1.5 Hz), 7.25-7.31 (3H, m), 7.37-7.40 (1H, m), 7.51-7.56 (2H, m), 8.01 (1H, d, J=8.1 Hz), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 472(1) and malonic acid; Yield: 75% (whitish-pink solid).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.2 Hz), 1.41-1.54 (2H, m), 1.71-1.80 (2H, m), 3.94 (2H, t, J=6.6 Hz), 6.58-6.63 (3H, m), 6.68-6.71 (1H, m), 7.09 (1H, d, J=1.5 Hz), 7.21-7.27 (3H, m), 7.34 (1H, dd, J=1.5, 8.1 Hz), 7.49-7.53 (2H, m), 7.72 (1H, d, J=8.1 Hz), 8.11 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 472(2); Yield: 80% (white solid).
1H-NMR (DMSO-d6) δ: 0.90 (3H, t, J=7.2 Hz), 1.36-1.45 (2H, m), 1.61-1.70 (2H, m), 2.54 (2H, t, J=7.8 Hz), 2.82 (2H, t, J=7.8 Hz), 3.93 (2H, t, J=6.6 Hz), 6.47-6.54 (2H, m), 6.67 (1H, dd, J=2.1, 8.4 Hz), 7.18-7.27 (2H, m), 7.39-7.46 (4H, m), 7.70-7.73 (2H, m), 12.19 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-(tert-butoxy)phenol; Yield: 85% (yellowish-white solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 7.00-7.07 (5H, m), 7.24-7.28 (2H, m), 7.33-7.37 (1H, m), 7.48-7.53 (2H, m), 8.00 (1H, d, J=8.1 Hz), 10.56 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 473(1) and malonic acid; Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 1.35 (9H, s), 6.63 (1H, d, J=15.9 Hz), 6.98-7.00 (5H, m), 7.23-7.28 (2H, m), 7.30 (1H, dd, J=1.8, 8.4 Hz), 7.47-7.50 (2H, m), 7.70 (1H, d, J=8.4 Hz), 8.15 (1H, d, J=15.9 Hz), 10.56 (1H, s).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 473(2); Yield: 88% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.53 (2H, t, J=7.8 Hz), 2.85 (2H, t, J=7.8 Hz), 6.90-6.99 (4H, m), 7.10-7.12 (1H, m), 7.39-7.43 (4H, m), 7.67-7.70 (2H, m), 12.25 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-trifluoromethylphenol; Yield: 67% (white solid).
1H-NMR (CDCl3) δ: 7.15-7.19 (2H, m), 7.26-7.40 (3H, m), 7.48-7.52 (1H, m), 7.55-7.58 (2H, m), 7.65-7.68 (2H, m), 8.06 (1H, d, J=8.1 Hz), 10.44 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 474(1) and malonic acid; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 6.58 (1H, d, J=15.9 Hz), 7.08-7.11 (2H, m), 7.15 (1H, d, J=1.8 Hz), 7.26-7.33 (2H, m), 7.44 (1H, dd, J=1.8, 8.1 Hz), 7.52-7.56 (2H, m), 7.60-7.63 (2H, m), 7.78 (1H, d, J=8.1 Hz), 8.02 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 474(2); Yield: 37% (white solid).
1H-NMR (DMSO-d6) δ: 2.53 (2H, t, J=7.8 Hz), 2.79 (2H, t, J=7.8 Hz), 7.11-7.13 (2H, m), 7.38-7.59 (5H, m), 7.72-7.80 (4H, m), 12.21 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-(tert-pentyl)phenol; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 0.70 (3H, t, J=7.2 Hz), 1.31 (6H, s), 1.65 (2H, q, J=7.2 Hz), 7.03-7.08 (3H, m), 7.22-7.28 (2H, m), 7.33-7.37 (3H, m), 7.50-7.54 (2H, m), 8.01 (1H, d, J=7.8 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 475(1) and malonic acid; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 0.70 (3H, t, J=7.2 Hz), 1.29 (6H, s), 1.64 (2H, q, J=7.2 Hz), 6.63 (1H, d, J=15.9 Hz), 6.97-7.00 (2H, m), 7.06 (1H, d, J=1.8 Hz), 7.23-7.27 (2H, m), 7.31-7.33 (3H, m), 7.48-7.52 (2H, m), 7.72 (1H, d, J=8.1 Hz), 8.15 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 475(2); Yield: 78% (white solid).
1H-NMR (DMSO-d6) δ: 0.62 (3H, t, J=7.2 Hz), 1.23 (6H, s), 1.58 (2H, q, J=7.2 Hz), 2.54 (2H, t, J=7.8 Hz), 2.84 (2H, t, J=7.8 Hz), 6.90-6.92 (2H, m), 7.15 (1H, s), 7.30-7.33 (2H, m), 7.39-7.44 (4H, m), 7.68-7.72 (2H, m), 12.18 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 2-naphthol; Yield: 80% (yellow solid).
1H-NMR (CDCl3) δ: 7.11 (1H, d, J=1.5 Hz), 7.22-7.26 (2H, m), 7.34 (1H, dd, J=2.4, 8.7 Hz), 7.40-7.54 (6H, m), 7.74-7.77 (1H, m), 7.86-7.89 (1H, m), 7.92 (1H, d, J=8.7 Hz), 8.06 (1H, d, J=8.1 Hz), 10.58 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 476(1) and malonic acid; Yield: 84% (white solid).
1H-NMR (CDCl3) δ: 6.65 (1H, d, J=16.2 Hz), 7.10 (1H, d, J=2.1 Hz), 7.22-7.24 (2H, m), 7.30 (1H, dd, J=2.1, 8.7 Hz), 7.36-7.51 (6H, m), 7.72-7.78 (2H, m), 7.83-7.90 (2H, m), 8.17 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 476(2); Yield: 68% (white solid).
1H-NMR (DMSO-d6) δ: 2.58 (2H, t, J=7.8 Hz), 2.88 (2H, t, J=7.8 Hz), 7.26-7.51 (9H, m), 7.71-7.74 (2H, m), 7.79-7.82 (1H, m), 7.90-7.93 (1H, m), 7.98 (1H, d, J=9.0 Hz), 12.22 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-(trifluoromethoxy)phenol; Yield: 91% (yellow solid).
1H-NMR (CDCl3) δ: 7.03 (1H, d, J=1.8 Hz), 7.08-7.15 (2H, m), 7.26-7.33 (2H, m), 7.36 (1H, ddd, J=0.6, 1.8, 8.4 Hz), 7.81 (1H, d, J=8.4 Hz), 10.44 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 477(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 98% (pale yellow solid).
1H-NMR (CDCl3) δ: 7.07-7.18 (3H, m), 7.21-7.34 (4H, m), 7.44 (1H, ddd, J=0.9, 1.8, 8.4 Hz), 7.50-7.59 (2H, m), 8.03 (1H, d, J=8.4 Hz), 10.48 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 477(2) and malonic acid; Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 6.60 (1H, d, J=16.2 Hz), 7.02-7.12 (3H, m), 7.18-7.32 (4H, m), 7.38 (1H, dd, J=1.8, 8.4 Hz), 7.50-7.59 (2H, m), 7.75 (1H, d, J=8.4 Hz), 8.10 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 477(1) and 4-(tert-butyl)phenylboronic acid; Yield: 98% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.09-7.16 (3H, m), 7.21-7.29 (2H, m), 7.43-7.51 (5H, m), 8.01 (1H, d, J=8.4 Hz), 10.47 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 478(1) and malonic acid; Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.58 (1H, d, J=16.2 Hz), 7.02-7.09 (2H, m), 7.11 (1H, d, J=1.5 Hz), 7.16-7.27 (2H, m), 7.40-7.50 (5H, m), 7.73 (1H, d, J=8.4 Hz), 8.09 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 477; Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 2.73 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 6.92-7.03 (2H, m), 7.06 (1H, d, J=1.8 Hz), 7.15-7.28 (4H, m), 7.29 (1H, dd, J=1.8, 7.8 Hz), 7.38 (1H, d, J=7.8 Hz), 7.45-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 478; Yield: 91% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.72 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 6.94-7.02 (2H, m), 7.09 (1H, brs), 7.12-7.20 (2H, m), 7.30-7.36 (2H, m), 7.40-7.47 (4H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-butylphenol; Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.31-1.44 (2H, m), 1.57-1.69 (2H, m), 2.60-2.69 (2H, m), 6.95-7.05 (3H, m), 7.20-7.27 (2H, m), 7.28 (1H, ddd, J=0.9, 1.8, 8.4 Hz), 7.78 (1H, d, J=8.4 Hz), 10.49 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 481(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 90% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.30-1.44 (2H, m), 1.55-1.68 (2H, m), 2.58-2.67 (2H, m), 7.00-7.06 (3H, m), 7.18-7.30 (4H, m), 7.35 (1H, ddd, J=0.9, 1.8, 8.4 Hz), 7.46-7.55 (2H, m), 7.99 (1H, d, J=8.4 Hz), 10.55 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 481(2); Yield: 88% (pale brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.30-1.44 (2H, m), 1.52-1.67 (2H, m), 2.55-2.65 (2H, m), 5.67 (1H, s), 6.94-7.02 (2H, m), 7.05 (1H, d, J=2.4 Hz), 7.10 (1H, d, J=8.4 Hz), 7.13-7.26 (5H, m), 7.40-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 481(3) and ethyl bromoacetate; Yield: 65% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.27 (3H, t, J=7.2 Hz), 1.28-1.44 (2H, m), 1.52-1.65 (2H, m), 2.54-2.62 (2H, m), 4.23 (2H, q, J=7.2 Hz), 4.72 (2H, s), 6.90-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.09-7.17 (2H, m), 7.16 (1H, d, J=1.8 Hz), 7.19-7.29 (3H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 481(4); Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=7.2 Hz), 1.28-1.44 (2H, m), 1.52-1.65 (2H, m), 2.54-2.62 (2H, m), 4.72 (2H, s), 6.90-6.98 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.09-7.17 (2H, m), 7.16 (1H, d, J=1.8 Hz), 7.19-7.29 (3H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and methyl 4-chloro-2-methylbutyrate; Yield: 81% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.29 (3H, d, J=7.2 Hz), 1.92-2.08 (1H, m), 2.22-2.38 (1H, m), 2.71-2.86 (1H, m), 3.70 (3H, s), 4.10-4.28 (2H, m), 7.07 (1H, d, J=8.7 Hz), 7.24-7.34 (2H, m), 7.54-7.64 (2H, m), 7.75 (1H, dd, J=2.4, 8.7 Hz), 8.04 (1H, d, J=2.4 Hz), 10.52 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 482(1); Yield: 92% (yellow solid).
1H-NMR (CDCl3) δ: 1.27 (3H, d, J=7.2 Hz), 1.92-2.10 (1H, m), 2.16-2.33 (1H, m), 2.66-2.83 (1H, m), 3.72 (3H, s), 4.12 (2H, t, J=6.0 Hz), 6.03 (1H, brs), 6.89 (1H, d, J=8.4 Hz), 7.01 (1H, dd, J=2.4, 8.4 Hz), 7.15 (1H, d, J=2.4 Hz), 7.19-7.30 (2H, m), 7.48-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 482(2) and p-(tert-butyl)benzyl bromide; Yield: 67% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (3H, d, J=7.2 Hz), 1.33 (9H, s), 1.84-2.02 (1H, m), 2.16-2.34 (1H, m), 2.73-2.91 (1H, m), 3.67 (3H, s), 4.02-4.18 (2H, m), 5.13 (2H, s), 6.96 (1H, d, J=8.1 Hz), 7.06-7.14 (2H, m), 7.19-7.28 (2H, m), 7.37-7.44 (4H, m), 7.44-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 482(3); Yield: 87% (white solid).
1H-NMR (CDCl3) δ: 1.23 (3H, d, J=6.9 Hz), 1.30 (9H, s), 1.82-2.00 (1H, m), 2.14-2.30 (1H, m), 2.69-2.86 (1H, m), 4.00-4.17 (1H, m), 5.11 (2H, s), 6.92 (1H, d, J=8.1 Hz), 7.04 (1H, dd, J=2.1, 8.1 Hz), 7.08 (1H, d, J=2.1 Hz), 7.15-7.24 (2H, m), 7.32-7.47 (6H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 2,5-dichlorophenylboronic acid; Yield: 95% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 6.98 (1H, d, J=1.5 Hz), 7.02-7.07 (2H, m), 7.18-7.21 (1H, m), 7.25-7.29 (2H, m), 7.36-7.42 (3H, m), 8.00 (1H, d, J=7.8 Hz), 10.56 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 483(1) and malonic acid. Yield: 84% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 6.69 (1H, d, J=16.2 Hz), 6.97-6.99 (3H, m), 7.29 (1H, d, J=8.1 Hz), 7.41-7.60 (5H, m), 7.83 (1H, d, J=16.2 Hz), 8.01 (1H, d, J=8.1 Hz), 12.53 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 483; Yield: 100% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 2.57 (2H, t, J=7.5 Hz), 2.87 (2H, t, J=7.5 Hz), 6.87-6.94 (3H, m), 7.18 (1H, d, J=7.5 Hz), 7.37-7.46 (5H, m), 7.56 (1H, d, J=8.4 Hz), 12.22 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 3-nitrophenylboronic acid; Yield: 55% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.24 (2H, q, J=7.2 Hz), 4.74 (2H, s), 6.93-6.98 (2H, m), 7.06 (1H, d, J=8.7 Hz), 7.27 (1H, d, J=2.4 Hz), 7.31-7.37 (3H, m), 7.55 (1H, t, J=7.8 Hz), 7.78-7.81 (1H, m), 8.13-8.16 (1H, m), 8.33-8.36 (1H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 485(1); Yield: 66% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.80 (2H, s), 6.86-6.90 (2H, m), 7.19 (1H, d, J=8.7 Hz), 7.31-7.35 (2H, m), 7.50 (1H, d, J=2.1 Hz), 7.61 (1H, dd, J=2.1, 8.7 Hz), 7.70 (1H, t, J=8.1 Hz), 8.08-8.18 (2H, m), 8.37 (1H, t, J=2.1 Hz), 13.12 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 315(2) and 3-aminophenylboronic acid; Yield: 53% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.31 (9H, s), 3.71 (2H, brs), 4.22 (2H, q, J=7.2 Hz), 4.71 (2H, s), 6.61-6.64 (1H, m), 6.79 (1H, t, J=1.8 Hz), 6.86-6.90 (1H, m), 6.92-6.97 (2H, m), 7.00 (1H, d, J=8.1 Hz), 7.15 (1H, d, J=7.8 Hz), 7.19-7.21 (1H, m), 7.27-7.34 (3H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 486(1); Yield: 77% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.74 (2H, s), 6.48-6.51 (1H, m), 6.67-6.73 (2H, m), 6.85-6.89 (2H, m), 7.04 (1H, d, J=7.8 Hz), 7.09 (1H, d, J=8.4 Hz), 7.14 (1H, d, J=2.1 Hz), 7.32-7.35 (3H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 4-bromo-2-methoxybenzaldehyde and 4-(trifluoromethoxy)phenylboronic acid; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 4.01 (3H, s), 7.13 (1H, d, J=1.2 Hz), 7.18-7.26 (1H, m), 7.29-7.38 (2H, m), 7.58-7.70 (2H, m), 7.91 (1H, d, J=7.8 Hz), 10.49 (1H, s).
The title compound was obtained in the same manner as the Example 83(1) using the following starting material.
Starting material: the intermediate 487(1); Yield: 48% (white solid).
1H-NMR (CDCl3) δ: 7.18 (1H, d, J=1.8 Hz), 7.22 (1H, dd, J=1.8, 8.1 Hz), 7.29-7.37 (2H, m), 7.61-7.69 (3H, m), 9.94 (1H, s), 11.14 (1H, s).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 487(2) and benzyl 3-bromopropyl ether; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 2.10-2.26 (2H, m), 3.70 (2H, t, J=6.0 Hz), 4.29 (2H, t, J=6.0 Hz), 4.54 (2H, s), 7.14 (1H, d, J=1.2 Hz), 7.16-7.38 (8H, m), 7.58-7.68 (2H, m), 7.90 (1H, d, J=7.8 Hz), 10.44 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 487(3) and malonic acid; Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 2.13-2.27 (2H, m), 3.73 (2H, t, J=6.0 Hz), 4.26 (2H, t, J=6.0 Hz), 4.54 (2H, s), 6.58 (1H, d, J=15.9 Hz), 7.11 (1H, d, J=1.5 Hz), 7.17 (1H, d, J=1.5, 7.8 Hz), 7.21-7.38 (8H, m), 7.55-7.66 (2H, m), 8.08 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 487; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 2.08-2.21 (2H, m), 2.67 (3H, t, J=7.8 Hz), 2.95 (2H, t, J=7.8 Hz), 3.70 (2H, t, J=6.3 Hz), 4.18 (2H, t, J=6.3 Hz), 4.54 (2H, s), 7.01 (1H, d, J=1.5 Hz), 7.06 (1H, dd, J=1.5, 7.5 Hz), 7.20-7.36 (8H, m), 7.52-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 487(2) and 3-chloropropyl phenyl sulfide; Yield: 87% (yellow solid).
1H-NMR (CDCl3) δ: 2.13-2.30 (2H, m), 3.17 (2H, t, J=6.9 Hz), 4.27 (2H, t, J=6.0 Hz), 7.08 (1H, d, J=1.5 Hz), 7.12-7.41 (8H, m), 7.55-7.64 (2H, m), 7.89 (1H, d, J=7.8 Hz), 10.49 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 489(1) and malonic acid; Yield: 93% (pale yellow solid).
1H-NMR (CDCl3) δ: 2.16-2.29 (2H, m), 3.19 (2H, t, J=6.9 Hz), 4.24 (2H, t, J=6.0 Hz), 6.58 (1H, d, J=16.2 Hz), 7.05 (1H, d, J=1.5 Hz), 7.12-7.22 (2H, m), 7.22-7.34 (4H, m), 7.34-7.42 (2H, m), 7.54-7.66 (3H, m), 8.12 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 2-(isopropyl)phenol; Yield: 59% (pale brown oil).
1H-NMR (CDCl3) δ: 1.23 (6H, d, J=7.2 Hz), 3.18 (1H, sept, J=7.2 Hz), 6.87 (1H, d, J=1.8 Hz), 6.92-6.99 (1H, m), 7.22-7.30 (3H, m), 7.38-7.44 (1H, m), 7.79 (1H, d, J=8.4 Hz), 10.56 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 490(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 99% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=7.2 Hz), 3.30 (1H, sept, J=7.2 Hz), 6.88 (1H, d, J=1.8 Hz), 6.92-7.02 (1H, m), 7.19-7.30 (5H, m), 7.38-7.52 (3H, m), 8.01 (1H, d, J=8.4 Hz), 10.62 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 490(2) and malonic acid; Yield: 70% (white solid).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=7.2 Hz), 3.29 (1H, sept, J=7.2 Hz), 6.66 (1H, d, J=15.9 Hz), 6.87 (1H, d, J=1.8 Hz), 6.87-6.93 (2H, m), 7.14-7.32 (4H, m), 7.36-7.50 (3H, m), 7.72 (1H, d, J=8.4 Hz), 8.21 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 490; Yield: 40% (white solid).
1H-NMR (CDCl3) δ: 1.27 (6H, d, J=7.2 Hz), 2.78 (2H, t, J=7.2 Hz), 3.09 (2H, t, J=7.2 Hz), 3.29 (1H, sept, J=7.2 Hz), 6.80-6.85 (2H, m), 6.86 (1H, d, J=1.8 Hz), 7.09-7.24 (4H, m), 7.32-7.39 (2H, m), 7.40-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-(benzyloxy)phenol; Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 5.09 (2H, s), 6.93 (1H, d, J=1.8 Hz), 7.04 (4H, s), 7.22-7.28 (1H, m), 7.31-7.48 (5H, m), 7.77 (1H, d, J=8.4 Hz), 10.51 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 492(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 73% (white solid).
1H-NMR (CDCl3) δ: 5.08 (2H, s), 6.96 (1H, d, J=1.8 Hz), 6.98-7.10 (4H, m), 7.22-7.28 (2H, m), 7.30-7.53 (8H, m), 7.99 (1H, d, J=8.4 Hz), 10.58 (1H, d, J=0.9 Hz).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 492(2); Yield: 66% (white solid).
1H-NMR (CDCl3) δ: 5.06 (2H, s), 5.70 (1H, s), 6.94-7.12 (6H, m), 7.14-7.24 (3H, m), 7.30-7.49 (7H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 492(3) and ethyl bromoacetate; Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 1.28 (3H, t, J=7.2 Hz), 4.24 (2H, q, J=7.2 Hz), 4.73 (2H, s), 5.04 (2H, s), 6.92-7.04 (5H, m), 7.08 (1H, d, J=1.8 Hz), 7.17-7.25 (3H, m), 7.30-7.49 (7H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 492(4); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 4.77 (2H, s), 5.06 (2H, s), 6.92-7.04 (4H, m), 7.13 (1H, d, J=8.1 Hz), 7.21 (1H, d, J=2.4 Hz), 7.28-7.49 (8H, m), 7.63-7.69 (2H, m), 13.06 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 492; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 4.76 (2H, s), 6.76-6.86 (2H, m), 6.90-6.99 (2H, m), 7.01-7.10 (2H, m), 7.17-7.28 (4H, m), 7.41-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 3,5-dimethylphenol; Yield: 92% (pale yellow solid).
1H-NMR (CDCl3) δ: 2.34 (6H, s), 6.70 (2H, s), 6.88 (1H, s), 7.00 (1H, d, J=1.8 Hz), 7.29 (1H, dd, J=1.8, 8.1 Hz), 7.78 (1H, d, J=8.1 Hz), 10.46 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 494(1) and 4-(tert-butyl)phenylboronic acid; Yield: 91% (pale yellow oil).
1H-NMR (CDCl3) δ: 1H-NMR (CDCl3) δ: 1.34 (9H, s), 2.31 (6H, s), 6.71 (2H, s), 6.81 (1H, s), 7.10 (1H, d, J=1.8 Hz), 7.50 (1H, dd, J=1.8, 8.1 Hz), 7.35-7.50 (4H, m), 7.98 (1H, d, J=8.1 Hz), 10.46 (1H, d, J=0.6 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 494(2) and malonic acid; Yield: 85% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.25 (6H, s), 6.60-6.80 (5H, m), 7.15 (1H, d, J=1.8 Hz), 7.42-7.50 (2H, m), 7.51-7.59 (2H, m), 7.76 (1H, d, J=16.2 Hz), 7.96 (1H, d, J=8.1 Hz), 12.42 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 4-(tert-butyl)phenylboronic acid; Yield: 94% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.34 (9H, s), 7.01-7.06 (2H, m), 7.12 (1H, d, J=1.7 Hz), 7.38-7.45 (7H, m), 7.98 (1H, d, J=8.1 Hz), 10.52 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 495(1) and malonic acid; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.33 (18H, s), 6.60 (1H, d, J=16.1 Hz), 6.95-7.00 (2H, m), 7.22 (1H, d, J=1.8 Hz), 7.33-7.39 (3H, m), 7.41-7.47 (4H, m), 7.69 (1H, d, J=8.2 Hz), 8.13 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 3,5-methyphenylboronic acid; Yield: 72% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.34 (6H, s), 7.00-7.05 (3H, m), 7.10-7.15 (3H, m), 7.37-7.42 (3H, m), 7.98 (1H, d, J=7.1 Hz), 10.50 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 496(1) and malonic acid; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.35 (6H, s), 6.61 (1H, d, J=16.1 Hz), 6.95-7.01 (3H, m), 7.09-7.16 (3H, m), 7.34-7.39 (3H, m), 7.70 (1H, d, J=8.1 Hz), 8.13 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 495; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 1.33 (9H, s), 2.74 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 6.89-6.94 (2H, m), 7.08 (1H, d, J=1.7 Hz), 7.26-7.35 (4H, m), 7.38-7.45 (4H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 496; Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.33 (6H, s), 2.73 (2H, t, J=7.3 Hz), 3.01 (2H, t, J=7.3 Hz), 6.88-6.93 (2H, m), 6.95 (1H, brs), 7.10 (3H, brs), 7.26-7.34 (4H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 494; Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.27 (6H, s), 2.72 (2H, t, J=7.2 Hz), 2.97 (2H, t, J=7.2 Hz), 6.60 (2H, s), 6.71 (1H, s), 7.08 (1H, d, J=1.5 Hz), 7.24-7.34 (2H, m), 7.37-7.48 (4H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 487(2) and (1-bromoethyl)benzene; Yield: 84% (white solid).
1H-NMR (CDCl3) δ: 1.75 (3H, d, J=6.6 Hz), 5.51 (1H, q, J=6.6 Hz), 6.99 (1H, d, J=1.5 Hz), 7.10-7.17 (1H, m), 7.21-7.48 (9H, m), 7.88 (1H, d, J=8.1 Hz), 10.66 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 500(1) and malonic acid; Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 1.76 (3H, d, J=6.3 Hz), 5.47 (1H, q, J=6.3 Hz), 6.67 (1H, d, J=16.2 Hz), 6.93 (1H, d, J=1.8 Hz), 7.09 (1H, dd, J=1.8, 8.1 Hz), 7.19-7.33 (3H, m), 7.33-7.46 (6H, m), 7.59 (1H, d, J=8.1 Hz), 8.24 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 500; Yield: 68% (white solid).
1H-NMR (CDCl3) δ: 1.67 (3H, d, J=6.3 Hz), 2.78 (2H, t, J=7.5 Hz), 3.08 (2H, t, J=7.5 Hz), 5.39 (1H, q, J=6.3 Hz), 6.85 (1H, d, J=1.5 Hz), 6.98 (1H, dd, J=1.5, 7.8 Hz), 7.14-7.43 (10H, m).
The title compound was obtained in the same manner as the Example 447(2) using the following starting materials.
Starting materials: 1-bromo-4-(tert-butoxy)benzene and trimethyl borate; Yield: 32% (white solid).
1H-NMR (DMSO-d6) δ: 1.31 (9H, s), 6.96 (2H, d, J=8.4 Hz), 7.78 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediates 502(1) and 315 (2); Yield: 62% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.24 Hz), 1.31 (9H, s), 1.35 (9H, s), 4.22 (2H, q, J=7.2 Hz), 4.70 (2H, s), 6.92-6.96 (2H, m), 6.97-7.02 (2H, m), 7.01 (1H, d, J=8.1 Hz), 7.22 (1H, d, J=2.4 Hz), 7.25-7.33 (3H, m), 7.35-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 502(2); Yield: 80% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 1.30 (9H, s), 4.74 (2H, s), 6.87 (2H, d, J=8.7 Hz), 6.99 (2H, d, J=8.4 Hz), 7.10 (1H, d, J=8.4 Hz), 7.26 (1H, d, J=2.4 Hz), 7.32 (2H, d, J=8.7 Hz), 7.40-7.45 (1H, m), 7.49 (2H, d, J=8.4 Hz), 13.04 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 90% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.02-7.09 (3H, m), 7.22-7.27 (1H, m), 7.33-7.48 (6H, m), 8.02 (1H, d, J=8.1 Hz), 10.54 (1H, d, J=0.7 Hz).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 503(1) and malonic acid; Yield: 90% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.62 (1H, d, J=16.1 Hz), 6.97-7.02 (2H, m), 7.09 (1H, d, J=1.8 Hz), 7.19-7.24 (1H, m), 7.31-7.44 (6H, m), 7.74 (1H, d, J=8.2 Hz), 8.14 (1H, d, J=16.1 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 503; Yield: 91% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.75 (2H, t, J=7.3 Hz), 3.04 (2H, t, J=7.3 Hz), 6.90-6.95 (2H, m), 7.07 (1H, d, J=1.7 Hz), 7.14-7.18 (1H, m), 7.24-7.27 (1H, m), 7.32-7.41 (6H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 314(3) and 4-butylphenylboronic acid; Yield: 84% (colorless oil).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.25 (3H, t, J=7.2 Hz), 1.30-1.47 (2H, m), 1.32 (9H, s), 1.55-1.69 (2H, m), 2.61-2.70 (2H, m), 4.22 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.93-7.04 (3H, m), 7.13-7.20 (2H, m), 7.21-7.29 (2H, m), 7.30-7.37 (2H, m), 7.43-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 505(1); Yield: 91% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.31 (9H, s), 1.32-1.46 (2H, m), 1.56-1.69 (2H, m), 2.61-2.70 (2H, m), 4.74 (2H, s), 6.93-7.04 (3H, m), 7.13-7.20 (2H, m), 7.21-7.29 (2H, m), 7.30-7.37 (2H, m), 7.43-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 487(2) and α-bromodiphenylmethane; Yield: 62% (yellow oil).
1H-NMR (CDCl3) δ: 6.41 (1H, s), 7.11 (1H, d, J=1.5 Hz), 7.14-7.55 (14H, m), 7.60-7.68 (1H, m), 7.92 (1H, d, J=8.1 Hz), 10.67 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 506(1) and malonic acid; Yield: 24% (white solid).
1H-NMR (CDCl3) δ: 6.38 (1H, s), 6.61 (1H, d, J=16.2 Hz), 7.07 (1H, d, J=1.8 Hz), 7.14 (1H, dd, J=1.8, 8.4 Hz), 7.18-7.55 (14H, m), 7.63 (1H, d, J=8.1 Hz), 8.26 (1H, d, J=16.2 Hz), 10.75 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 506; Yield: 52% (white solid).
1H-NMR (CDCl3) δ: 2.77 (2H, d, J=7.8 Hz), 3.11 (2H, d, J=7.8 Hz), 6.31 (1H, s), 6.94-7.00 (1H, m), 7.00-7.06 (1H, m), 7.15-7.41 (11H, m), 7.41-7.51 (4H, m), 11.26 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 489; Yield: 30% (white solid).
1H-NMR (CDCl3) δ: 2.08-2.27 (2H, m), 2.70 (2H, t, J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz), 3.16 (2H, t, J=6.9 Hz), 4.16 (2H, t, J=6.9 Hz), 6.97 (1H, d, J=1.5 Hz), 7.06 (1H, dd, J=1.5, 7.8 Hz), 7.12-7.43 (8H, m), 7.50-7.63 (2H, m), 10.70 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-isopropylphenol; Yield: 84% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (6H, d, J=6.9 Hz), 2.83-3.02 (1H, m), 7.00-7.10 (3H, m), 7.20-7.31 (4H, m), 7.31-7.40 (1H, m), 7.46-7.56 (2H, m), 8.01 (1H, d, J=8.4 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 509(1) and malonic acid; Yield: 73% (white solid).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=6.9 Hz), 2.83-3.02 (1H, m), 6.63 (1H, d, J=16.2 Hz), 6.87-7.01 (2H, m), 7.06 (1H, d, J=1.8 Hz), 7.09-7.35 (5H, m), 7.46-7.55 (2H, m), 7.72 (1H, d, J=8.1 Hz), 8.15 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 509; Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 1.25 (6H, d, J=6.9 Hz), 2.75 (2H, t, J=7.8 Hz), 2.81-2.97 (1H, m), 3.04 (2H, t, J=7.8 Hz), 6.88-6.96 (2H, m), 7.04 (1H, d, J=1.8 Hz), 7.14-7.31 (5H, m), 7.35 (1H, d, J=7.8 Hz), 7.44-7.52 (2H, m), 9.90 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-butylphenol; Yield: 45% (yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.26-1.45 (2H, m), 1.52-1.72 (2H, m), 2.63 (2H, t, J=7.2 Hz), 6.98-7.11 (3H, m), 7.16-7.42 (5H, m), 7.45-7.59 (2H, m), 8.00 (1H, d, J=8.1 Hz), 10.54 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 511(1) and malonic acid; Yield: 58% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.29-1.45 (2H, m), 1.53-1.69 (2H, m), 2.61 (2H, t, J=7.8 Hz), 6.63 (1H, d, J=16.2 Hz), 6.72-7.01 (2H, m), 7.03 (1H, d, J=1.5 Hz), 7.13-7.36 (5H, m), 7.44-7.55 (2H, m), 7.71 (1H, d, J=8.1 Hz), 8.15 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 511; Yield: 59% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.5 Hz), 1.28-1.44 (2H, m), 1.52-1.66 (2H, m), 2.59 (2H, t, J=7.8 Hz), 2.75 (2H, t, J=7.8 Hz), 3.04 (2H, t, J=7.8 Hz), 6.84-6.95 (2H, m), 7.02 (1H, d, J=2.1 Hz), 7.09-7.17 (2H, m), 7.17-7.28 (3H, m), 7.35 (1H, d, J=8.1 Hz), 7.42-7.52 (2H, m), 10.02 (1H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 490(2); Yield: 90% (brown oil).
1H-NMR (CDCl3) δ: 1.27 (6H, d, J=6.6 Hz), 3.34 (1H, sept, J=6.6 Hz), 5.70 (1H, s), 6.87 (1H, d, J=2.1 Hz), 6.88-6.95 (1H, m), 7.11 (1H, d, J=8.4 Hz), 7.15-7.24 (5H, m), 7.35-7.44 (3H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 513(1) and ethyl bromoacetate; Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.28 (6H, d, J=6.6 Hz), 3.42 (1H, sept, J=6.6 Hz), 4.23 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.80-6.87 (1H, m), 7.00-7.14 (4H, m), 7.17-7.25 (3H, m), 7.31-7.38 (1H, m), 7.41-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 513(2); Yield: 60% (colorless oil).
1H-NMR (CDCl3) δ: 1.28 (6H, d, J=6.6 Hz), 3.39 (1H, sept, J=6.6 Hz), 4.76 (2H, s), 6.80-6.86 (1H, m), 7.00-7.16 (4H, m), 7.18-7.27 (3H, m), 7.32-7.39 (1H, m), 7.41-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 465(1) and 3-(trifluoromethoxy)phenylboronic acid; Yield: 87% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.87-6.90 (1H, m), 7.08 (1H, d, J=1.5 Hz), 7.20-7.27 (3H, m), 7.31-7.47 (5H, m), 8.02 (1H, d, J=8.4 Hz), 10.56 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 514(1) and malonic acid; Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 6.69 (1H, d, J=16.2 Hz), 6.77 (1H, ddd, J=1.2, 2.4, 8.1 Hz), 7.17-7.41 (5H, m), 7.56-7.71 (4H, m), 7.82 (1H, d, J=16.2 Hz), 8.03 (1H, d, J=8.1 Hz), 12.49 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 514; Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.55 (2H, t, J=7.5 Hz), 2.86 (2H, t, J=7.5 Hz), 6.69-6.74 (1H, m), 7.09-7.17 (3H, m), 7.28 (1H, d, J=8.1 Hz), 7.32-7.35 (1H, m), 7.44-7.50 (2H, m), 7.53-7.64 (3H, m), 12.00 (1H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-isopropylbenzenethiol; Yield: 87% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.27 (6H, d, J=6.9 Hz), 2.88-3.02 (1H, m), 7.20-7.30 (5H, m), 7.40-7.51 (5H, m), 7.94 (1H, d, J=8.1 Hz), 10.41 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 516(1) and malonic acid; Yield: 67% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.24 (6H, d, J=6.9 Hz), 2.90 (1H, sept, J=6.9 Hz), 6.44 (1H, d, J=15.9 Hz), 7.18-7.31 (6H, m), 7.46-7.52 (4H, m), 7.73 (1H, d, J=8.4 Hz), 8.42 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 462; Yield: 40% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.72 (2H, t, J=7.8 Hz), 3.16 (2H, t, J=7.8 Hz), 7.19-7.25 (4H, m), 7.30-7.49 (7H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 79(1) and 4-(isopropyl)phenylboronic Acid; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=6.6 Hz), 1.34 (9H, s), 2.93 (1H, sept, J=6.6 Hz), 7.01-7.06 (2H, m), 7.11 (1H, d, J=1.5 Hz), 7.29 (2H, d, J=8.4 Hz), 7.37-7.46 (5H, m), 7.98 (1H, d, J=8.1 Hz), 10.52 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 518(1) and malonic acid; Yield: 92% (white solid).
1H-NMR (DMSO-d6) δ: 1.20 (6H, d, J=6.9 Hz), 1.27 (9H, s), 2.90 (1H, sept, J=6.6 Hz), 6.64 (1H, d, J=16.0 Hz), 6.94-6.98 (2H, m), 7.18 (1H, d, J=1.8 Hz), 7.30 (2H, d, J=8.1 Hz), 7.38-7.42 (2H, m), 7.50-7.58 (3H, m), 7.80 (1H, d, J=16.0 Hz), 7.98 (1H, d, J=8.1 Hz), 12.46 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 518; Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 1.20 (6H, d, J=6.9 Hz), 1.27 (9H, s), 2.54 (2H, t, J=7.2 Hz), 2.83 (2H, t, J=7.2 Hz), 2.90 (1H, sept, J=6.9 Hz), 6.88-6.92 (2H, m), 7.06-7.10 (1H, m), 7.28 (2H, d, J=8.4 Hz), 7.36-7.43 (4H, m), 7.47 (2H, d, J=8.4 Hz), 12.19 (1H, brs).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzaldehyde and 4-isopropylphenylboronic acid; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.30 (6H, d, J=6.9 Hz), 2.98 (1H, sept, J=6.9 Hz), 7.32-7.43 (3H, m), 7.47-7.52 (1H, m), 7.53-7.58 (2H, m), 7.92 (1H, t, J=7.8 Hz), 10.38 (1H, s).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 520(1) and 4-(tert-butyl)benzenethiol; Yield: 86% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.26 (6H, d, J=6.9 Hz), 1.34 (9H, m), 2.93 (1H, sept, J=6.9 Hz), 7.23-7.30 (3H, m), 7.36-7.44 (6H, m), 7.52 (1H, dd, J=1.8, 7.8 Hz), 7.92 (1H, d, J=7.8 Hz), 10.41 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 520(2) and malonic acid; Yield: 80% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.27 (6H, d, J=7.2 Hz), 1.30 (9H, m), 2.94 (1H, sept, J=7.2 Hz), 6.42 (1H, d, J=15.9 Hz), 7.24-7.35 (6H, m), 7.44 (2H, d, J=8.4 Hz), 7.52 (1H, dd, J=1.8, 8.1 Hz), 7.56 (1H, d, J=1.8 Hz), 7.72 (1H, d, J=8.1 Hz), 8.43 (1H, d, J=15.9 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediates 79(1) and 447(1); Yield: 88% (yellow oil).
1H-NMR (CDCl3) δ: 0.95 (6H, t, J=7.2 Hz), 1.34 (9H, s), 1.62-1.75 (4H, m), 4.09-4.20 (1H, m), 6.88-6.98 (2H, m), 6.98-7.06 (2H, m), 7.08 (1H, d, J=1.8 Hz), 7.32-7.51 (5H, m), 7.97 (1H, d, J=7.8 Hz), 10.50 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 521(1) and malonic acid; Yield: 81% (pale yellow solid).
1H-NMR (CDCl3) δ: 0.95 (6H, t, J=7.5 Hz), 1.33 (9H, s), 1.61-1.74 (4H, m), 4.07-4.19 (1H, m), 6.59 (1H, d, J=16.2 Hz), 6.86-7.02 (4H, m), 7.08 (1H, d, J=1.8 Hz), 7.28-7.48 (5H, m), 7.68 (1H, d, J=8.4 Hz), 8.13 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 521; Yield: 85% (white solid).
1H-NMR (CDCl3) δ: 0.95 (6H, t, J=7.5 Hz), 1.31 (9H, s), 1.61-1.74 (4H, m), 2.73 (2H, t, J=7.8 Hz), 3.01 (2H, t, J=7.8 Hz), 4.04-4.18 (1H, m), 6.85-6.96 (4H, m), 7.06 (1H, d, J=1.5 Hz), 7.23 (1H, dd, J=1.5, 8.1 Hz), 7.27-7.36 (3H, m), 7.38-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 75(1) using the following starting materials.
Starting materials: the intermediate 333(1) and 4-butoxyphenol; Yield: 88% (yellow oil).
1H-NMR (CDCl3) δ: 0.99 (3H, t, J=7.2 Hz), 1.40-1.59 (2H, m), 1.70-1.85 (2H, m), 3.97 (2H, t, J=6.3 Hz), 6.89-7.00 (3H m), 7.02-7.12 (2H, m), 7.20-7.37 (3H, m), 7.44-7.54 (2H, m), 7.99 (1H, d, J=8.1 Hz), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 523(1); Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 0.98 (3H, t, J=6.9 Hz), 1.40-1.58 (2H, m), 1.70-1.84 (2H, m), 3.94 (2H, t, J=6.6 Hz), 5.78 (1H, s), 6.84-6.93 (2H m), 6.95-7.05 (2H, m), 7.09 (1H, d, J=8.1 Hz), 7.14-7.24 (3H, m), 7.38-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 523(2) and ethyl bromoacetate; Yield: 96% (colorless oil).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.2 Hz), 1.27 (3H, t, J=7.2 Hz), 1.40-1.57 (2H, m), 1.68-1.83 (2H, m), 3.93 (2H, t, J=7.2 Hz), 4.24 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.82-6.92 (2H m), 6.95-7.05 (3H, m), 7.07 (1H, d, J=2.4 Hz), 7.15-7.26 (3H, m), 7.40-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 523(3); Yield: 55% (white solid).
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.5 Hz), 1.40-1.58 (2H, m), 1.67-1.83 (2H, m), 3.93 (2H, t, J=6.6 Hz), 4.71 (2H, s), 6.80-6.92 (2H m), 6.93-7.10 (4H, m), 7.14-7.30 (3H, m), 7.37-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 514(1); Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 5.75 (1H, brs), 6.81-6.85 (1H, m), 7.10-7.20 (5H, m), 7.24-7.31 (3H, m), 7.35-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 524(1) and ethyl bromoacetate; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.24 (2H, q, J=7.2 Hz), 4.73 (2H, s), 6.77 (1H, ddd, J=1.2, 2.4, 8.1 Hz), 7.02 (1H, t, J=8.4 Hz), 7.04-7.16 (3H, m), 7.21-7.31 (4H, m), 7.37-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 524(2); Yield: 62% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.78 (2H, s), 6.60-6.72 (1H, m), 7.05-7.25 (4H, m), 7.28-7.35 (1H, m), 7.42 (1H, d, J=2.4 Hz), 7.51-7.59 (3H, m), 7.62-7.69 (1H, m), 13.09 (1H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 463(1); Yield: 89% (brown oil).
1H-NMR (CDCl3) δ: 5.62 (1H, s), 6.94-6.98 (2H, m), 7.05-7.09 (2H, m), 7.16 (1H, dd, J=2.2, 8.6 Hz), 7.20-7.23 (1H, m), 7.37-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 525(1) and ethyl bromoacetate; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.1 Hz), 4.21 (2H, q, J=7.1 Hz), 4.65 (2H, s), 6.83 (1H, d, J=8.8 Hz), 6.98-7.02 (2H, m), 7.06-7.13 (2H, m), 7.18 (1H, dd, J=2.4, 8.6 Hz), 7.37-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 525(2) and phenylboronic acid; Yield: 68% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 4.23 (2H, q, J=7.1 Hz), 4.70 (2H, s), 6.97-7.90 (4H, m), 7.25-7.42 (7H, m), 7.47-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 525(3); Yield: 78% (pale yellow solid).
1H-NMR (CDCl3) δ: 4.73 (2H, s), 6.99-7.14 (4H, m), 7.27-7.44 (7H, m), 7.48-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 525(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 63% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.1 Hz), 4.23 (2H, q, J=7.1 Hz), 4.71 (2H, s), 6.97-7.11 (4H, m), 7.20-7.36 (6H, m), 7.46-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 526(1); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 4.74 (2H, s), 6.99-7.15 (4H, m), 7.22-7.39 (6H, m), 7.48-7.52 (2H, m).
A mixture of the intermediate 110(1) (300 mg, 0.723 mmol), (methoxymethyl)triphenylphosphonium chloride (545 mg, 1.59 mmol), potassium tert-butoxide (162 mg, 1.45 mmol) and anhydrous N,N-dimethylformamide (3 ml) was stirred at 60° C. for 1 hour. A saturated aqueous solution of ammonium chloride and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (320 mg, 100%) as a colorless oil. This compound was obtained as a mixture of the geometric isomers.
1H-NMR (CDCl3) δ: [1.30 (s), 1.31 (s), 9H in total], [3.65 (s), 3.81 (s), 3H in total], [5.59 (d, J=6.9 Hz), 5.99 (d, J=12.9 Hz), 1H in total], [6.19 (d, J=7.2 Hz), 6.85-6.95 (m), 7.07-7.04 (m), 7.18-7.38 (m), 7.44 (d, J=8.1 Hz), 7.47-7.56 (m), 8.21 (d, J=8.1 Hz), 12H in total].
A mixture of the intermediate 527(1) (320 mg, 0.723 mmol), 2 N hydrochloric acid (2 ml) and tetrahydrofuran (4 ml) was refluxed for 6 hours. The reaction mixture was cooled to room temperature, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (176 mg, 57%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.37 (9H, s), 3.79 (2H, d, J=1.5 Hz), 6.88-6.97 (2H, m), 7.09-7.02 (1H, m), 7.20-7.28 (2H, m), 7.28-7.39 (4H, m), 7.44-7.55 (2H, m), 9.80 (1H, t, J=1.5 Hz).
The title compound was obtained in the same manner as the Example 26(1) using the following starting materials.
Starting materials: the intermediate 527(2) and triethyl phosphonoacetate; Yield: 87% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.32 (9H, s), 3.59 (2H, d, J=6.9 Hz), 4.17 (2H, q, J=7.2 Hz), 5.83 (1H, d, J=15.6 Hz), 6.87-6.95 (2H, m), 7.07-7.11 (1H, m), 7.11 (1H, d, J=6.9, 15.6 Hz), 7.21-7.30 (4H, m), 7.30-7.39 (2H, m), 7.46-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 527(3); Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.2 Hz), 1.32 (9H, s), 2.00 (2H, quint, J=7.5 Hz), 2.35 (2H, t, J=7.5 Hz), 2.73 (2H, t, J=7.5 Hz), 4.11 (2H, q, J=7.2 Hz), 6.87-6.94 (2H, m), 7.06-7.10 (1H, m), 7.20-7.28 (2H, m), 7.30-7.38 (4H, m), 7.47-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 527(4); Yield: 89% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.00 (2H, quint, J=7.5 Hz), 2.40 (2H, t, J=7.5 Hz), 2.75 (2H, t, J=7.5 Hz), 6.87-6.94 (2H, m), 7.07 (1H, d, J=2.1 Hz), 7.20-7.28 (3H, m), 7.29-7.38 (3H, m), 7.46-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 333(1) and thiophenol; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 7.22-7.29 (3H, m), 7.37-7.53 (8H, m), 7.96 (1H, d, J=7.8 Hz), 10.42 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 528(1) and malonic acid; Yield: 94% (yellow solid).
1H-NMR (DMSO-d6) δ: 6.61 (1H, d, J=15.9 Hz), 7.24-7.47 (7H, m), 7.71 (1H, d, J=1.8 Hz), 7.76-7.80 (3H, m), 8.05 (1H, d, J=8.1 Hz), 8.07 (1H, d, J=15.9 Hz), 12.57 (1H, brs).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 462(1) and bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.66 (3H, s), 5.98 (1H, d, J=12.3 Hz), 7.21-7.33 (7H, m), 7.42-7.53 (4H, m), 7.61 (1H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 529(1); Yield: 91% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 6.49 (1H, d, J=12.3 Hz), 7.19 (1H, d, J=12.3 Hz), 7.24-7.27 (2H, m), 7.37-7.49 (5H, m), 7.56-7.65 (2H, m), 7.69-7.72 (2H, m), 12.48 (1H, brs).
A mixture of methyl methylsulfinylmethyl sulfide (115 mg, 0.929 mmol) and sodium hydroxide was stirred at 70° C. for 30 minutes, and the intermediate 462(1) (200 mg, 0.465 mmol) was added to the mixture, followed by refluxing for 1.5 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (0.172 g, 69%) as a white solid.
1H-NMR (CDCl3) δ: 1.28 (9H, s), 2.12 (3H, s), 2.58 (3H, s) 7.19-7.36 (6H, m), 7.50-7.60 (3H, m), 7.62 (1H, d, J=2.1 Hz), 7.95 (1H, d, J=8.1 Hz), 8.04 (1H, s).
A solution of the intermediate 530(1) (0.172 g, 0.320 mmol) in a 2 N solution of hydrochloric acid-ethanol (5 ml) was refluxed for 7 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (0.031 g, 20%) as a white solid.
1H-NMR (CDCl3) δ: 1.23 (3H, t, J=7.2 Hz), 1.28 (9H, s), 3.88 (2H, s), 4.12 (2H, q, J=7.2 Hz), 7.13-7.21 (2H, m), 7.21-7.34 (4H, m), 7.40 (1H, d, J=7.8 Hz), 7.44-7.55 (3H, m), 7.58 (1H, d, J=1.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 530(2); Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.93 (2H, s), 7.14-7.34 (6H, m), 7.39 (1H, d, J=7.8 Hz), 7.44-7.54 (3H, m), 7.57 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 431(2) using the following starting material.
Starting material: the intermediate 79(1); Yield: 100% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.99-4.04 (2H, m), 4.12-4.17 (2H, m), 6.13 (1H, s), 6.93-6.98 (2H, m), 7.16-7.28 (2H, m), 7.34-7.39 (2H, m), 7.48 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 418(1) using the following starting materials.
Starting materials: the intermediate 531(1) and 4-(trifluoromethoxy)aniline; Yield: 83% (brown oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.98-4.07 (2H, m), 4.13-4.18 (2H, m), 5.75 (1H, brs), 6.10 (1H, s), 6.47 (1H, d, J=2.4 Hz), 6.79 (1H, dd, J=2.4, 8.1 Hz), 6.91-6.99 (4H, m), 7.02-7.04 (2H, m), 7.31-7.35 (2H, m), 7.50 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 431(5) using the following starting material.
Starting material: the intermediate 531(2); Yield: 68% (white solid).
1H-NMR (CDCl3) δ: 1.38 (9H, s), 6.13 (1H, brs), 6.30 (1H, d, J=2.1 Hz), 6.69 (1H, dd, J=1.5, 8.7 Hz), 6.98-7.03 (2H, m), 7.07-7.15 (4H, m), 7.37-7.41 (2H, m), 7.83 (1H, d, J=8.7 Hz), 10.30 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 531(3) and malonic acid; Yield: 97% (pale brown solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 6.39 (1H, d, J=16.2 Hz), 6.42 (1H, d, J=3.0 Hz), 6.85 (1H, dd, J=2.4, 8.4 Hz), 7.00 (2H, d, J=9.0 Hz), 7.12 (2H, d, J=9.0 Hz), 7.22 (2H, d, J=9.0 Hz), 7.44 (2H, d, J=9.0 Hz), 7.72 (1H, d, J=98.4 Hz), 7.76 (1H, d, J=16.2 Hz), 8.84 (1H, s), 12.16 (1H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 531; Yield: 80% (pale brown solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 2.48 (2H, t, J=7.2 Hz), 2.75 (2H, t, J=7.2 Hz), 6.45 (1H, d, J=2.1 Hz), 6.81 (1H, dd, J=2.1, 8.4 Hz), 6.84-6.94 (2H, m), 7.00-7.05 (2H, m), 7.13-7.19 (3H, m), 7.36-7.41 (2H, m), 8.35 (1H, s).
A mixture of the intermediate 6313(3) (1.11 g, 2.77 mmol), n-butyryl chloride (0.347 ml, 3.32 mmol), sodium hydrogen carbonate (698 mg, 8.31 mmol), dichloromethane (5 ml) and water (5 ml) was stirred at room temperature for 1 hour. The reaction mixture was diluted with water, and extracted with chloroform. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with a mixture of n-hexane and diisopropyl ether to give the title compound (1.17 g, 90%) as a white solid.
1H-NMR (CDCl3) δ: 0.98 (3H, t, J=7.5 Hz), 1.33 (9H, s), 1.65-1.79 (2H, m), 2.32-2.39 (2H, m), 6.95-7.02 (2H, m), 7.06 (1H, d, J=2.1 Hz), 7.19-7.25 (2H, m), 7.31 (1H, dd, J=2.1, 8.4 Hz), 7.35-7.42 (2H, m), 7.44-7.51 (2H, m), 7.77 (1H, brs), 8.55 (1H, d, J=8.4 Hz).
A solution of the intermediate 533(1) (1.17 g, 2.49 mmol) in anhydrous tetrahydrofuran (2 ml) was added dropwise to a suspension of lithium aluminium hydride (283 mg, 7.47 mmol) in anhydrous tetrahydrofuran (5 ml), and the mixture was refluxed for 3 hours. The reaction mixture was cooled to 0° C., followed by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (1.13 g, 99%) as a brown oil.
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.5 Hz), 1.31 (9H, s), 1.32-1.47 (2H, m), 1.53-1.68 (2H, m), 3.13-3.24 (2H, m), 4.35 (1H, brs), 6.78 (1H, d, J=8.4 Hz), 6.90-6.98 (2H, m), 7.07 (1H, d, J=1.8 Hz), 7.15-7.22 (2H, m), 7.25 (1H, dd, J=1.8, 8.4 Hz), 7.30-7.36 (2H, m), 7.42-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 533(2) and ethyl iodoacetate; Yield: 82% (brown oil).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=7.5 Hz), 1.17 (3H, t, J=7.2 Hz), 1.23-1.34 (2H, m), 1.30 (9H, s), 1.41-1.53 (2H, m), 3.25-3.33 (2H, m), 4.06 (2H, q, J=7.2 Hz), 4.08 (2H, s), 6.81-6.88 (2H, m), 7.12-7.32 (7H, m), 7.45-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 533(3); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.2 Hz), 1.24-1.38 (2H, m), 1.32 (9H, s), 1.44-1.57 (2H, m), 3.12-3.20 (2H, m), 3.81 (2H, s), 6.90-6.97 (2H, m), 7.12 (1H, d, J=1.8 Hz), 7.21-7.31 (4H, m), 7.32-7.39 (2H, m), 7.44-7.51 (2H, m).
A mixture of the intermediate 442(3) (1.11 g, 2.77 mmol), di-tert-butyl dicarbonate (1.81 g, 8.31 nmol), a 4 N solution of sodium hydroxide (5 ml) and tetrahydrofuran (5 ml) was refluxed for 6 hours. 2 N hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (1.24 g, 89%) as a brown oil.
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.53 (9H, s), 6.95-7.02 (2H, m), 7.05 (1H, d, J=2.1 Hz), 7.16 (1H, brs), 7.18-7.25 (2H, m), 7.29 (1H, dd, J=1.8, 8.4 Hz), 7.34-7.41 (2H, m), 7.42-7.50 (2H, m), 8.27 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 533(2) using the following starting material.
Starting material: the intermediate 534(1); Yield: 23% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.90 (3H, d, J=4.8 Hz), 4.32 (1H, q, J=4.5 Hz), 6.78 (1H, d, J=8.4 Hz), 6.90-6.96 (2H, m), 7.09 (1H, d, J=1.8 Hz), 7.15-7.23 (2H, m), 7.27-7.36 (3H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the intermediate 534(2) and ethyl iodoacetate; Yield: 59% (colorless oil).
1H-NMR (CDCl3) δ: 1.17 (3H, t, J=7.2 Hz), 1.30 (9H, s), 3.03 (3H, s), 4.07 (2H, q, J=7.2 Hz), 4.12 (2H, s), 6.85-6.92 (2H, m), 7.09 (1H, d, J=2.1 Hz), 7.11 (1H, d, J=7.8 Hz), 7.16-7.23 (2H, m), 7.25-7.35 (3H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 534(3); Yield: 60% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.94 (3H, s), 3.85 (2H, s), 6.91-6.98 (2H, m), 7.12 (1H, d, J=2.1 Hz), 7.18-7.32 (4H, m), 7.32-7.39 (2H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 12(3) using the following starting materials.
Starting materials: the intermediate 531(3) and bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate; Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.72 (3H, s), 5.84 (1H, brs), 5.85 (1H, d, J=12.6 Hz), 6.44 (1H, d, J=2.1 Hz), 6.74 (1H, dd, J=2.1, 8.7 Hz), 6.90-6.95 (2H, m), 7.01-7.10 (4H, m), 7.17 (1H, d, J=12.6 Hz), 7.31-7.36 (2H, m), 7.90 (1H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 535(1); Yield: 87% (yellow solid).
1H-NMR (DMSO-d6) δ: 1.27 (9H, s), 5.81 (1H, d, J=12.9 Hz), 6.41 (1H, d, J=2.1 Hz), 6.80 (1H, dd, J=2.1, 8.4 Hz), 6.95-7.02 (3H, m), 7.09-7.12 (2H, m), 7.20 (2H, d, J=8.7 Hz), 7.40-7.44 (2H, m), 7.82 (1H, d, J=8.4 Hz), 8.70 (1H, s), 12.33 (1H, brs).
The title compound was obtained in the same manner as the Example 418(1) using the following starting materials.
Starting materials: the intermediate 315(2) and 4-(trifluoromethoxy)aniline; Yield: 33% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=6.9 Hz), 1.30 (9H, s), 4.21 (2H, q, J=6.9 Hz), 4.63 (2H, s), 5.63 (1H, brs), 6.67 (1H, d, J=2.7 Hz), 6.77 (1H, dd, J=2.7, 8.7 Hz), 6.86-6.96 (5H, m), 7.03 (2H, d, J=9.0 Hz), 7.29-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 536(1); Yield: 89.0% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.63 (2H, s), 6.62 (1H, d, J=2.7 Hz), 6.83-6.99 (6H, m), 7.14 (2H, d, J=8.4 Hz), 7.34-7.38 (2H, m), 8.18 (1H, s), 12.96 (1H, brs).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 312(1) and ethyl bromoacetate; Yield: 54% (colorless oil).
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.2 Hz), 1.32 (9H, s), 4.16 (2H, q, J=7.2 Hz), 4.62 (2H, s), 6.63-6.70 (1H, m), 6.89-6.99 (5H, m), 7.00-7.07 (1H, m), 7.13-7.22 (2H, m), 7.32-7.40 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 537(1); Yield: 69% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.66 (2H, s), 6.70-6.77 (1H, m), 6.89-6.98 (5H, m), 7.02-7.09 (1H, m), 7.12-7.22 (2H, m), 7.32-7.41 (2H, m).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 95(3) and benzyl bromide; Yield: 83% (pale yellow oil).
1H-NMR (CDCl3) δ: 5.20 (2H, s), 6.91-6.98 (2H, m), 7.07 (1H, d, J=9.0 Hz), 7.13-7.20 (2H, m), 7.24 (1H, dd, J=3.0, 9.0 Hz), 7.35-7.48 (5H, m), 7.50 (1H, d, J=3.0 Hz), 10.51 (1H, s).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 538(1); Yield: 53% (pale yellow oil).
1H-NMR (CDCl3) δ: 5.09 (2H, s), 6.82-6.90 (2H, m), 6.64-7.04 (4H, m), 7.14-7.20 (2H, m), 7.30-7.42 (4H, m), 8.25 (1H, s).
The title compound was obtained in the same manner as the Example 89(2) using the following starting materials.
Starting materials: the intermediate 538(2) and 4-(tert-butyl)phenylboronic acid; Yield: 50% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 5.08 (2H, s), 6.68-6.76 (2H, m), 6.87-7.04 (8H, m), 7.10-7.18 (2H, m), 7.17-7.42 (4H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 538(3); Yield: 50% (colorless oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 5.49 (1H, s), 6.61 (1H, d, J=2.7 Hz), 6.69 (1H, dd, J=2.7, 8.4 Hz), 6.85-6.94 (2H, m), 6.94-7.00 (2H, m), 7.02 (1H, d, J=8.4 Hz), 7.08-7.16 (2H, m), 7.30-7.39 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 538(4) and ethyl bromoacetate; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.23 (2H, q, J=7.2 Hz), 4.67 (2H, s), 6.64-6.73 (2H, m), 6.90-7.02 (5H, m), 7.10-7.20 (2H, m), 7.29-7.37 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 538(5); Yield: 81% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 4.70 (2H, s), 6.63-6.72 (2H, m), 6.91-6.99 (4H, m), 7.01 (1H, d, J=8.4 Hz), 7.11-7.19 (2H, m), 7.30-7.37 (2H, m).
The title compound was obtained in the same manner as the Example 416(1) using the following starting materials.
Starting materials: the compound 6 (3) and methyl bromoacetate; Yield: 47% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 4.04 (2H, s), 5.11 (2H, s), 6.68 (1H, d, J=1.5 Hz), 6.90-6.97 (2H, m), 7.21-7.28 (2H, m), 7.37-7.56 (6H, m).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediates 12(1) and 67 (3); Yield: 11% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.21 (3H, d, J=7.2 Hz), 1.37 (9H, s), 2.70 (2H, t, J=7.5 Hz), 3.07 (2H, t, J=7.5 Hz), 4.11 (2H, q, J=7.2 Hz), 6.95 (1H, d, J=8.4 Hz), 7.02 (1H, d, J=8.4 Hz), 7.27-7.32 (2H, m), 7.43-7.63 (8H, m), 7.70 (1H, dd, J=2.4, 8.7 Hz), 8.15 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 26(1) using the following starting materials.
Starting materials: the intermediate 540(1) and triethyl phosphonoacetate; Yield: 11% (white solid).
1H-NMR (CDCl3) δ: 1.21 (3H, d, J=6.9 Hz), 1.34 (3H, d, J=7.2 Hz), 1.37 (9H, s), 2.70 (2H, t, J=7.5 Hz), 3.06 (2H, t, J=7.5 Hz), 4.11 (2H, q, J=7.2 Hz), 4.27 (2H, q, J=6.9 Hz), 6.66 (1H, d, J=16.2 Hz), 6.86-6.94 (2H, m), 7.25-7.45 (2H, m), 7.41-7.60 (9H, m), 7.80 (1H, d, J=2.1 Hz), 8.09 (1H, d, J=16.2 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 540(2); Yield: 86% (white solid).
1H-NMR (DMSO-d6) δ: 1.32 (9H, s), 2.60 (2H, t, J=7.8 Hz), 2.92 (2H, t, J=7.8 Hz), 6.85 (1H, d, J=16.2 Hz), 6.87-6.96 (2H, m), 7.44-7.61 (7H, m), 7.66 (1H, d, J=2.4 Hz), 7.73 (1H, dd, J=2.4, 8.7 Hz), 7.86-7.91 (2H, m), 7.92 (1H, d, J=16.2 Hz), 8.21 (1H, d, J=2.4 Hz), 12.32 (2H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 540; Yield: 77% (white solid).
1H-NMR (DMSO-d6) δ: 1.32 (9H, s), 2.59-2.67 (4H, m), 2.91-3.00 (4H, m), 6.82-6.88 (2H, m), 7.42-7.69 (10H, m), 7.75-7.80 (2H, m), 12.17 (2H, brs).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 12(1) and 5-(tert-butyl)-2-hydroxybenzaldehyde; Yield: 59% (pale brown solid).
1H-NMR (CDCl3) δ: 1.37 (9H, s), 6.98 (1H, d, J=8.4 Hz), 7.00 (1H, d, J=8.4 Hz), 7.26-7.37 (2H, m), 7.56-7.69 (3H, m), 7.73 (1H, dd, J=2.4, 8.4 Hz), 8.02 (1H, d, J=2.4 Hz), 8.17 (1H, d, J=2.4 Hz), 10.47 (1H, s), 10.58 (1H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 542(1) and malonic acid; Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 1.25 (9H, s), 3.74 (2H, t, J=4.5 Hz), 3.97 (2H, s), 4.14 (2H, t, J=4.5 Hz), 7.23 (1H, d, J=8.4 Hz), 6.88-6.92 (3H, m), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 542(2); Yield: 80% (white solid).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 2.53 (2H, t, J=8.1 Hz), 2.62 (2H, t, J=8.1 Hz), 2.84 (2H, t, J=8.1 Hz), 2.96 (2H, t, J=8.1 Hz), 6.70 (1H, d, J=8.4 Hz), 6.75 (1H, d, J=8.4 Hz), 7.24 (1H, dd, J=2.4, 8.4 Hz), 7.34-7.54 (4H, m), 7.64 (1H, d, J=2.4 Hz), 7.70-7.82 (2H, m), 12.15 (2H, brs).
The title compound was obtained in the same manner as the Example 2(1) using the following starting materials.
Starting materials: the intermediate 18(1) and 1-bromo-5-chloropentane; Yield: 33% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.70-1.85 (2H, m), 1.93-2.09 (4H, m), 4.20 (4H, t, J=6.0 Hz), 7.08 (2H, d, J=8.5 Hz), 7.24-7.33 (4H, m), 7.54-7.62 (4H, m), 7.75 (2H, dd, J=2.5, 8.5 Hz), 8.04 (2H, d, J=2.5 Hz), 10.55 (2H, s).
The title compound was obtained in the same manner as the Example 2(3) using the following starting materials.
Starting materials: the intermediate 543(1) and malonic acid; Yield: 74% (white solid).
1H-NMR (DMSO-d6) δ: 1.58-1.75 (2H, m), 1.83-1.99 (4H, m), 4.17 (4H, t, J=6.0 Hz), 6.73 (2H, d, J=16.0 Hz), 7.20 (2H, d, J=8.5 Hz), 7.37-7.46 (4H, m), 7.70 (2H, dd, J=2.5, 8.5 Hz), 7.80-7.86 (4H, m), 7.89 (2H, d, J=16.0 Hz), 8.00 (2H, d, J=2.5 Hz), 12.32 (2H, brs).
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the compound 543; Yield: 66% (white solid).
1H-NMR (DMSO-d6) δ: 1.59-1.73 (2H, m), 1.78-1.93 (4H, m), 2.54 (4H, t, J=7.5 Hz), 2.86 (4H, t, J=7.5 Hz), 4.07 (4H, t, J=6.0 Hz), 7.05 (2H, d, J=8.5 Hz), 7.36-7.43 (4H, m), 7.44-7.51 (4H, m), 7.67-7.75 (4H, m), 12.06 (2H, brs).
The title compound was obtained in the same manner as the Example 95(2) using the following starting material.
Starting material: the intermediate 542(1); Yield: 37% (yellow solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 6.18 (2H, brs), 6.78-6.92 (3H, m), 6.96 (1H, dd, J=2.1, 8.7 Hz), 7.08 (1H, d, J=2.1 Hz), 7.18-7.30 (3H, m), 7.44-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting material.
Starting material: the intermediate 545(1); Yield: 55% (colorless oil).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.27 (3H, t, J=7.2 Hz), 1.31 (9H, s), 4.15-4.32 (4H, m), 4.71 (2H, s), 4.80 (2H, s), 6.84-6.96 (2H, m), 6.96-7.05 (2H, m) 7.05-7.16 (1H, m), 7.19 (1H, d, J=2.1 Hz), 7.22-7.30 (2H, m), 7.46-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 545(2); Yield: 60% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.19 (2H, s), 4.31 (2H, s), 6.95 (1H, dd, J=1.8, 8.4 Hz), 6.99-7.10 (2H, m), 7.12 (1H, d, J=1.8 Hz), 7.19 (1H, dd, J=1.8, 8.4 Hz), 7.34-7.39 (1H, m), 7.39-7.50 (2H, m), 7.75-7.86 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the compound 301 (3); Yield: 17% (colorless oil).
1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 4.25 (2H, s), 5.15 (2H, s), 6.70 (1H, d, J=2.1 Hz), 6.82 (1H, d, J=2.1 Hz), 7.38-7.46 (6H, m), 7.69-7.72 (2H, m).
A mixture of 4-bromo-2-fluorobenzoic acid (2.000 g, 9.132 mmol), concentrated sulfuric acid (2 ml) and methanol (20 ml) was refluxed for 2 hours. After the reaction mixture was cooled to room temperature, water was added to the residue obtained by evaporation of the solvent under reduced pressure, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was recrystallized from methanol to give the title compound (1.906 g, 90%) as a white solid.
1H-NMR (CDCl3) δ: 3.93 (3H, s), 7.31-7.40 (2H, m), 7.83 (1H, t, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 547(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 3.96 (3H, s), 7.28-7.38 (3H, m), 7.41 (1H, dd, J=2.1, 7.8 Hz), 7.58-7.67 (2H, m), 8.02 (1H, t, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 547(2) and 4-tert-butylbenzenethiol; Yield: 8% (white solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 3.98 (3H, s), 6.88 (1H, d, J=1.5 Hz), 7.11-7.20 (2H, m), 7.22-7.44 (3H, m), 7.44-7.52 (4H, m), 8.05 (1H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 547(3); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.37 (9H, s), 6.91 (1H, d, J=1.8 Hz), 7.14-7.21 (2H, m), 7.29-7.37 (3H, m), 7.47-7.59 (4H, m), 8.18 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: 4-bromo-2-fluorobenzonitrile and 4-(trifluoromethoxy)phenylboronic acid; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 7.23 (2H, m), 7.41 (1H, dd, J=1.5, 9.9 Hz), 7.46 (1H, dd, J=1.5, 8.1 Hz), 7.57-7.68 (2H, m), 7.71 (1H, dd, J=6.6, 8.1 Hz).
The title compound was obtained in the same manner as the Example 12(2) using the following starting materials.
Starting materials: the intermediate 548(1) and 4-tert-butylbenzenethiol; Yield: 85% (white solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.21-7.29 (3H, m), 7.38-7.50 (7H, m), 7.70 (1H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 530(1) using the following starting materials.
Starting materials: the intermediate 548(2) and methyl (methylsulfinyl)methyl sulfide; Yield: 40% (yellow solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.39 (3H, s), 2.53 (3H, s) 5.45 (2H, brs), 7.17-7.55 (11H, m).
A mixture of the intermediate 548(3) (154 mg, 0.279 mmol), copper(II) chloride dihydrate (48 mg, 0.279 mmol) and ethanol (4 ml) was stirred at room temperature for 16 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (8 mg, 6%) as a yellow solid.
1H-NMR (CDCl3) δ: 1.35 (9H, s), 1.42 (3H, t, J=7.2 Hz), 4.44 (2H, q, J=7.2 Hz), 7.12 (1H, d, J=1.8 Hz), 7.17-7.24 (2H, m), 7.33-7.44 (3H, m), 7.46 (4H, s), 7.89 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 548(4); Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 7.06 (1H, d, J=1.5 Hz), 7.14-7.24 (2H, m), 7.30-7.38 (2H, m), 7.41 (1H, dd, J=1.5, 8.1 Hz), 7.49 (4H, s), 8.54 (1H, d, J=8.1 Hz).
A mixture of the intermediate 18(1) (3.00 g, 10.6 mmol), tert-butyldimethylchlorosilane (1.76 g, 11.7 mmol), imidazole (0.941 g, 13.8 mmol) and dichloromethane (50 ml) was stirred at 0° C. for 18 hours. The reaction mixture was diluted with water, and extracted with dichloromethane. The organic layer was washed saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (3.26 g, 77%) as a colorless oil.
1H-NMR (CDCl3) δ: 0.32 (6H, s), 1.05 (9H, s), 6.97 (1H, d, J=8.4 Hz), 7.22-7.33 (2H, m), 7.52-7.62 (2H, m), 7.66 (1H, dd, J=2.7, 8.4 Hz), 8.02 (1H, d, J=2.4 Hz), 10.51 (1H, s).
A solution of n-butyllithium in hexane (2.50 ml, 4.00 mmol) was added dropwise to a solution of 1-bromo-4-(tert-butyl)benzene (1.28 g, 6.00 mmol) in anhydrous tetrahydrofuran (10 ml) at −78° C., and the mixture was stirred for 30 minutes. A solution of the intermediate 549(1) (793 mg, 2.00 mmol) in anhydrous tetrahydrofuran (1 ml) was added dropwise to the reaction mixture at −78° C., and the mixture was stirred for 1 hours. A saturated aqueous solution of ammonium chloride and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (1.01 g, 95%) as a colorless oil.
1H-NMR (CDCl3) δ: 0.23 (6H, s), 0.90 (9H, s), 1.29 (9H, s), 2.67 (1H, d, J=5.4 Hz), 6.10 (1H, d, J=5.4 Hz), 6.89 (1H, d, J=8.4 Hz), 7.20-7.40 (6H, m), 7.49-7.58 (4H, m).
A mixture of the intermediate 549(2) (2.47 g, 4.65 mmol), pyridinium dichromate (2.62 g, 9.30 mmol), silica gel (10 g) and chloroform (40 ml) was refluxed for 3 hours. The reaction mixture was filtered, and the residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=10:1) to give the title compound (2.36 g, 96%) as a pale yellow oil.
1H-NMR (CDCl3) δ: 0.08 (6H, s), 0.64 (9H, s), 1.33 (9H, s), 6.94 (1H, d, J=8.4 Hz), 7.22-7.29 (3H, m), 7.41-7.49 (2H, m), 7.53-7.62 (3H, m), 7.75-7.83 (2H, m).
A solution of tetrabutylammonium fluoride in tetrahydrofuran (5.35 ml, 5.35 mmol) was added to a solution of the intermediate 549(3) (2.36 g, 4.46 mmol) in tetrahydrofuran (5 ml) at 0° C., and the mixture was stirred for 1 hour. 2 N hydrochloric acid and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with a mixture of n-hexane and diisopropyl ether to give the title compound (2.36 g, 62%) as a white solid.
1H-NMR (CDCl3) δ: 1.38 (9H, s), 7.17 (1H, d, J=8.4 Hz), 7.21-7.29 (2H, m), 7.42-7.52 (2H, m), 7.52-7.58 (2H, m), 7.66-7.75 (3H, m), 7.83 (1H, d, J=2.4 Hz), 12.06 (1H, s).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 549(4) and ethyl bromoacetate; Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.34 (9H, s), 4.20 (2H, q, J=7.2 Hz), 4.61 (2H, s), 6.94 (1H, d, J=8.4 Hz), 7.21-7.30 (2H, m), 7.43-7.50 (2H, m), 7.51-7.59 (3H, m), 7.61 (1H, dd, J=2.4, 8.4 Hz), 7.82-7.89 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 549(5); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 1.37 (9H, s), 4.85 (2H, s), 7.20 (1H, d, J=8.4 Hz), 7.24-7.31 (2H, m), 7.49-7.57 (4H, m), 7.62 (1H, d, J=2.4 Hz), 7.73 (1H, dd, J=2.4, 8.4 Hz), 7.84-7.90 (2H, m).
A mixture of the intermediate 549(300 mg, 0.635 mmol), 10% palladium on activated carbon (34 mg, 5 mol %), 2 N hydrochloric acid (0.1 ml) and methanol (5 ml) was stirred for 18 hours under hydrogen atmosphere. The reaction mixture was filtered. The residue obtained by concentration of the filtrate under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (64 mg, 22%) as a white solid.
1H-NMR (CDCl3) δ: 1.29 (9H, s), 4.07 (2H, s), 4.68 (2H, s), 6.85 (1H, d, J=8.4 Hz), 7.15-7.28 (4H, m), 7.28-7.34 (2H, m), 7.35-7.42 (2H, m), 7.48-7.55 (2H, m).
A mixture of 4-(tert-butyl)benzyl bromide (1.01 ml, 5.50 mmol), triphenylphosphine (1.31 g, 5.00 mmol) and anhydrous tetrahydrofuran was refluxed for 3 hours. The reaction mixture was cooled to room temperature. The precipitated solid was collected by filtration, and washed with diethyl ether to give the title compound (2.31 g, 94%) as a white solid.
1H-NMR (CDCl3) δ: 1.23 (9H, s), 5.35 (2H, d, J=14.1 Hz), 6.98-7.04 (2H, m), 7.10-7.20 (2H, m), 7.54-7.83 (15H, m).
The title compound was obtained in the same manner as the Example 26(1) using the following starting materials.
Starting materials: the intermediates 549(1) and 551(1); Yield: 64% (pale yellow oil).
This compound was obtained as a mixture of the geometric isomers.
1H-NMR (CDCl3) δ: [0.26 (s), 0.27 (s), 6H in total], [1.02 (s), 1.09 (s), 9H in total], [1.31 (s), 1.32 (s), 9H in total], [6.60-6.73 (m), 6.85-6.93 (m), 7.22-7.53 (m), 7.57-7.64 (m), 7.78 (d, J=2.4 Hz), 13H in total].
The title compound was obtained in the same manner as the Example 3 using the following starting material.
Starting material: the intermediate 551(2); Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 0.29 (6H, s), 1.06 (9H, s), 1.32 (9H, s), 2.83-2.98 (4H, m), 6.87 (1H, d, J=8.4 Hz), 7.09-7.17 (2H, m), 7.17-7.36 (6H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 549(4) using the following starting material.
Starting material: the intermediate 551(3); Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 2.87-3.03 (4H, m), 4.70-4.73 (1H, m), 6.83 (1H, d, J=8.4 Hz), 7.11-7.18 (2H, m), 7.18-7.36 (6H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 105(2) using the following starting materials.
Starting materials: the intermediate 551(4) and ethyl bromoacetate; Yield: 64% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.33 (3H, t, J=7.2 Hz), 2.88-3.07 (4H, m), 4.29 (2H, q, J=7.2 Hz), 4.65 (2H, s), 6.79 (1H, d, J=8.4 Hz), 7.11-7.18 (2H, m), 7.18-7.36 (6H, m), 7.42-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 551(5); Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.87-3.07 (4H, m), 4.66 (2H, s), 6.82 (1H, d, J=8.4 Hz), 7.08-7.14 (2H, m), 7.20-7.33 (5H, m), 7.34 (1H, dd, J=2.4, 8.4 Hz), 7.42-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromo-2-fluoroaniline and benzyl bromide; Yield: 80% (pale yellow oil).
1H-NMR (CDCl3) δ: 4.29 (1H, s), 4.34 (2H, s), 6.48-6.54 (1H, m), 7.02-7.39 (7H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 601(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 83% (pale yellow solid).
1H-NMR (CDCl3) δ: 4.39 (1H, s), 4.41 (2H, s), 6.67-6.75 (1H, m), 7.15-7.51 (11H, m).
The title compound was obtained in the same manner as the Example 219(1) using the following starting materials.
Starting materials: the intermediate 601(2) and succinic acid monoethyl ester chloride; Yield: 88% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.2 Hz), 2.31-2.82 (4H, m), 4.14 (2H, q, J=7.2 Hz), 4.54 (1H, d, J=14.4 Hz), 5.27 (1H, d, J=14.4 Hz), 7.03-7.10 (1H, m), 7.19-7.34 (9H, m), 7.52-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 601(3); Yield: 53% (white solid).
1H-NMR (CDCl3) δ: 2.25-2.65 (4H, m), 4.55 (1H, d, J=14.1 Hz), 5.04 (1H, d, J=14.4 Hz), 7.01-7.21 (10H, m), 7.40 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 219(1) using the following starting materials.
Starting materials: the intermediate 601(2) and ethyl malonyl chloride; Yield: 43% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=6.9 Hz), 3.28 (2H, s), 4.14 (2H, q, J=7.2 Hz), 4.51 (1H, d, J=14.4 Hz), 5.35 (1H, d, J=14.4 Hz), 7.22-7.35 (10H, m), 7.51-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 602(1); Yield: 13% (white solid).
1H-NMR (CDCl3) δ: 3.20 (2H, s), 4.58 (2H, s), 7.03-7.30 (10H, m), 7.41 (2H, d, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromobenzylamine hydrochloride and 4-(tert-butyl)benzyl bromide; Yield: 48% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.75 (2H, s), 3.76 (2H, s), 7.20-7.49 (8H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 603(1) and methyl chloroglyoxylate; Yield: 93% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (CDCl3) δ: [1.31 (s), 1.32 (s), 9H in total], [3.87 (s), 3.88 (s), 3H in total], [4.28 (s), 4.29 (s), 2H in total], [4.44 (s), 4.45 (s), 2H in total], [7.06-7.19 (m), 7.32-7.41 (m), 7.42-7.51 (m), 8H in total].
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 603(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 82% (pale brown oil).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (CDCl3) δ: [1.32 (s), 1.33 (s), 9H in total], [3.89 (s), 3.89 (s), 3H in total]. [4.34 (s), 4.38 (s), 2H in total], [4.50 (s), 4.54 (s), 2H in total], [7.06-7.66 (m), 7.06-7.66 (m) 12H in total].
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 603(3); Yield: 85% (white solid).
This compound was obtained as a mixture of the rotational isomers.
1H-NMR (DMSO-d6) δ: 1.26 (9H, m), 1.26 (9H, m), 4.27 (2H, m), 4.32 (2H, m), 4.40 (2H, m), 4.44 (2H, m), 7.10-7.18 (2H, m), 7.10-7.18 (2H, m), 7.26-7.38 (4H, m), 7.26-7.38 (4H, m), 7.41-7.50 (2H, m), 7.41-7.50 (2H, m), 7.73-7.83 (4H, m), 7.73-7.83 (4H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromoaniline and 4-(tert-butyl)benzyl bromide; Yield: 32% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.05 (1H, s), 4.25 (2H, d, J=3.3 Hz), 6.49-6.52 (2H, m), 7.21-7.39 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 604(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 22% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.12 (1H, brs), 4.34 (2H, s), 6.68-6.74 (2H, m), 7.17-7.26 (2H, m), 7.30-7.42 (6H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 219(1) using the following starting materials.
Starting materials: the intermediate 604(2) and ethyl glutaryl chloride; Yield: 100% (pale yellow solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 1.30 (3H, t, J=7.2 Hz), 1.70-2.48 (6H, m), 4.06 (2H, q, J=7.2 Hz), 4.87 (2H, s), 7.05-7.17 (4H, m), 7.26-7.42 (4H, m), 7.50-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 604(3); Yield: 23% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 1.90-2.00 (2H, m), 2.17 (2H, t, J=7.2 Hz), 2.33 (2H, t, J=7.2 Hz), 4.87 (2H, s), 7.05-7.17 (4H, m), 7.27-7.31 (4H, m), 7.49-7.61 (4H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 604(2) and methyl bromoacetate; Yield: 67% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.76 (3H, s), 4.13 (2H, s), 4.66 (2H, s), 6.73-6.79 (2H, m), 7.20-7.25 (4H, m), 7.34-7.45 (4H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 605(1); Yield: 63% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.22 (2H, s), 4.61 (2H, s), 6.63-6.72 (2H, m), 7.18-7.52 (8H, m), 7.61-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 4-(trifluoromethoxy)phenol and 4-fluoro-1-nitrobenzene; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 7.02-7.06 (2H, m), 7.10-7.14 (2H, m), 7.26-7.31 (2H, m), 8.21-8.25 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 606(1); Yield: 93% (yellow oil).
1H-NMR (CDCl3) δ: 3.61 (2H, brs), 6.67-6.70 (2H, m), 6.85-6.88 (2H, m), 6.89-6.92 (2H, m), 7.12 (2H, t, J=9.0 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 606(2) and 4-(tert-butyl)benzyl bromide; Yield: 56% (yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.94 (1H, brs), 4.28 (2H, s), 6.23-6.66 (2H, m), 6.88-6.92 (4H, m), 7.09-7.13 (2H, m), 7.30-7.33 (2H, m), 7.37-7.40 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 606(3) and methyl bromoacetate; Yield: 73% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 3.75 (3H, s), 4.08 (2H, s), 4.61 (2H, s), 6.66-6.70 (2H, m), 6.88-6.94 (4H, m), 7.09-7.13 (2H, m), 7.20-7.29 (2H, m), 7.35-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 606(4); Yield: 30% (brown oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 4.11 (2H, s), 4.59 (2H, s), 6.69-6.72 (2H, m), 6.88-6.94 (4H, m), 7.09-7.13 (2H, m), 7.20-7.23 (2H, m), 7.35-7.38 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 604(1) and ethyl 3-bromopropionate; Yield: 14% (colorless oil).
1H-NMR (CDCl3) δ: 1.21-1.32 (12H, m), 2.62 (2H, t, J=7.8 Hz), 3.73 (2H, t, J=7.8 Hz), 4.10 (2H, q, J=6.9 Hz), 4.51 (2H, s), 6.56-6.59 (2H, m), 7.08-7.11 (2H, m), 7.24-7.33 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 607(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 58% (colorless oil).
1H-NMR (CDCl3) δ: 1.22-1.31 (12H, m), 2.68 (2H, t, J=7.2 Hz), 3.81 (2H, t, J=7.2 Hz), 4.41 (2H, q, J=7.2 Hz), 4.59 (2H, s), 6.77-6.80 (2H, m), 7.15 (2H, d, J=8.4 Hz), 7.21 (2H, d, J=8.4 Hz), 7.32-7.35 (2H, m), 7.40-7.43 (2H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 607(2); Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 2.73 (2H, t, J=7.8 Hz), 3.79 (2H, t, J=7.8 Hz), 4.57 (2H, s), 6.80-6.84 (2H, m), 7.14-7.17 (2H, m), 7.20-7.24 (2H, m), 7.32-7.35 (2H, m), 7.41-7.45 (2H, m), 7.51-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 219(1) using the following starting materials.
Starting materials: the intermediate 604(2) and ethyl malonyl chloride; Yield: 52% (colorless oil).
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.2 Hz), 1.30 (9H, s), 3.27 (2H, s), 4.14 (2H, q, J=7.2 Hz), 4.92 (2H, s), 7.10-7.21 (4H, m), 7.26-7.33 (4H, m), 7.48-7.59 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 608(1); Yield: 65% (white solid).
1H-NMR (CDCl3) δ: 1.21 (9H, s), 3.23 (2H, s), 4.93 (2H, s), 7.06 (2H, d, J=8.4 Hz), 7.13 (2H, d, J=8.1 Hz), 7.18-7.26 (4H, m), 7.32 (2H, d, J=7.8 Hz), 7.37 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 219(1) using the following starting materials.
Starting materials: the intermediate 604(2) and ethyl succinyl chloride; Yield: 23% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=6.9 Hz), 1.29 (9H, s), 2.41 (2H, t, J=6.9 Hz), 2.65 (2H, t, J=6.9 Hz), 4.13 (2H, q, J=6.9 Hz), 4.88 (2H, s), 7.12-7.18 (4H, m), 7.26-7.31 (4H, m), 7.49-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 609(1); Yield: 49% (white solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 2.27 (2H, t, J=6.0 Hz), 2.66 (2H, t, J=6.0 Hz), 4.87 (2H, s), 7.09-7.15 (4H, m), 7.25-7.30 (4H, m), 7.51 (2H, d, J=8.1 Hz), 7.56 (2H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 153(2) and 1-bromo-4-(tert-butyl)benzene; Yield: 73% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 5.48 (1H, s), 6.88-7.12 (8H, m), 7.15-7.32 (4H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 610(1) and methyl bromoacetate; Yield: 98% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.68 (3H, s), 4.42 (2H, s), 6.87-6.95 (3H, m), 6.97-7.04 (5H, m), 7.13-7.28 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 610(2); Yield: 87% (white solid).
1H-NMR (DMSO-d6) δ: 1.26 (9H, s), 4.59 (2H, s), 6.72-6.80 (2H, m), 6.97-7.35 (10H, m), 12.91 (1H, brs).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: aniline and methyl chloroglyoxylate; Yield: 67% (white solid).
H-NMR (CDCl3) δ: 3.98 (3H, s), 7.20 (1H, t, J=7.5 Hz), 7.39 (2H, t, J=7.5 Hz), 7.64 (2H, d, J=7.5 Hz), 8.87 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 611(1) and 4-bromobenzyl bromide; Yield: 48% (colorless oil).
1H-NMR (CDCl3) δ: 3.54 (3H, s), 4.90 (2H, s), 7.00-7.17 (4H, m), 7.28-7.38 (3H, m), 7.38-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 611(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 71% (yellow oil).
1H-NMR (CDCl3) δ: 3.55 (3H, s), 4.99 (2H, s), 7.05-7.15 (2H, m), 7.22-7.39 (7H, m), 7.44-7.52 (2H, m), 7.53-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 611(3); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 4.93 (2H, s), 7.02-7.68 (11H, m), 7.75 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: 4-(tert-butyl)aniline and methyl chloroglyoxylate; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.98 (3H, s), 7.37-7.44 (2H, m), 7.53-7.60 (2H, m), 8.81 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 612(1) and 4-bromomethylbiphenyl; Yield: 45% (white solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.55 (3H, s), 4.96 (2H s), 6.98-7.06 (2H, m), 7.28-7.39 (5H, m), 7.39-7.48 (2H, m), 7.48-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 612(2); Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 1.23 (9H, s), 4.99 (2H, s), 7.03-7.78 (13H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 612(1) and 4-bromobenzyl bromide; Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.53 (3H, s), 4.86 (2H s), 7.12 (2H, d, J=8.5 Hz), 7.31 (2H, d, J=8.5 Hz), 7.42 (2H, d, J=8.5 Hz), 7.96 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 613(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 23% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 4.97 (2H, s), 6.97-7.07 (2H, m), 7.23-7.39 (6H, m), 7.50 (2H, d, J=8.2 Hz), 7.54-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 613(2); Yield: 62% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.90 (2H, s), 7.06-7.53 (8H, m), 7.53-7.68 (2H, m), 7.70-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 2,6-dichloroaniline and methyl chloroglyoxylate; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 4.01 (3H, s), 7.25 (1H, t, J=8.0 Hz), 7.41 (2H, d, J=8.0 Hz), 8.59 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 614(1) and 4-bromobenzyl bromide; Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 3.65 (3H, s), 4.89 (2H, s), 7.07-7.16 (2H, m), 7.18-7.27 (1H, m), 7.29-7.40 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 614(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 11% (colorless oil).
1H-NMR (CDCl3) δ: 3.65 (3H, s), 4.99 (2H, s), 7.15-7.38 (7H, m), 7.38-7.49 (2H, m), 7.51-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 614(3); Yield: 94% (white solid).
1H-NMR (DMSO-d6) δ: 4.82 (2H, s), 7.23-7.66 (9H, m), 7.70-7.87 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: 4-(trifluoromethoxy)aniline and methyl chloroglyoxylate; Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 3.99 (3H, s), 7.21-7.31 (2H, m), 7.65-7.75 (2H, m), 8.91 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 615(1) and 4-bromobenzyl bromide; Yield: 73% (white solid).
1H-NMR (CDCl3) δ: 3.57 (3H, s), 4.88 (2H, s), 7.03-7.14 (4H, m), 7.14-7.22 (2H, m), 7.38-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 615(2) and 4-(tert-butyl)phenylboronic acid; Yield: 29% (colorless oil).
1H-NMR (CDCl3) δ: 1.36 (9H, s), 3.57 (3H, s), 4.96 (2H, s), 7.06-7.23 (4H, m), 7.23-7.33 (2H, m), 7.42-7.49 (2H, m), 7.49-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 615(3); Yield: 42% (white solid).
1H-NMR (DMSO-d6) δ: 1.30 (9H, s), 4.94 (2H, s), 7.15-7.50 (8H, m), 7.50-7.67 (4H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 1-fluoro-4-nitrobenzene and 4-(trifluoromethoxy)benzyl alcohol; Yield: 85% (white solid).
1H-NMR (CDCl3) δ: 5.16 (2H, s), 7.00-7.07 (2H, m), 7.24-7.31 (2H, m), 7.44-7.51 (2H, m), 8.19-8.26 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 616(1); Yield: 97% (gray solid).
1H-NMR (CDCl3) δ: 3.47 (2H, brs), 4.98 (2H, s), 6.62-6.68 (2H, m), 6.76-6.84 (2H, m), 7.19-7.25 (2H, m), 7.41-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 616(2) and methyl chloroglyoxylate; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 3.97 (3H, s), 5.06 (2H, s), 6.93-7.00 (2H, m), 7.21-7.28 (2H, m), 7.43-7.49 (2H, m), 7.54-7.61 (2H, m), 8.78 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 616(3) and 4-(tert-butyl)benzyl bromide; Yield: 71% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.54 (3H, s), 4.86 (2H, s), 5.01 (2H, s), 6.83-6.90 (2H, m), 6.96-7.03 (2H, m), 7.11-7.17 (2H, m), 7.20-7.27 (2H, m), 7.28-7.33 (2H, m), 7.41-7.47 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 616(4); Yield: 95% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.82 (2H, s), 5.07 (2H, s), 6.94-7.01 (2H, m), 7.05-7.15 (4H, m), 7.26-7.42 (4H, m), 7.51-7.59 (2H, m), 13.87 (1H, brs).
Phosphoryl chloride (0.931 ml, 9.90 mmol) was added dropwise to a solution of 4-nitrobenzoic acid (1.50 g, 9.00 mmol) in anhydrous tetrahydrofuran (5 ml) at 0° C., and the mixture was stirred for 30 minutes. Then 4-(trifluoromethoxy)aniline (1.75 g, 9.90 mmol) and pyridine (0.801 g, 9.90 mmol) were added to the mixture at 0° C., and the mixture was stirred at room temperature for 1 hour. 2 N hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was washed with diisopropyl ether to give the title compound (1.41 g, 48%) as a white solid.
1H-NMR (CDCl3) δ: 7.22-7.30 (2H, m), 7.65-7.73 (2H, m), 7.89 (1H, brs), 8.01-8.07 (2H, m), 8.33-8.39 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 617(1); Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 5.81 (2H, brs), 6.57-6.64 (2H, m), 7.28-7.35 (2H, m), 7.69-7.75 (2H, m), 7.83-7.90 (2H, m), 9.95 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 617(2) and 4-(tert-butyl)benzyl bromide; Yield: 68% (white solid).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 4.36 (2H, s), 4.48 (1H, brs), 6.62-6.69 (2H, m), 7.16-7.23 (2H, m), 7.28-7.44 (4H, m), 7.60-7.76 (5H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 617(3) and methyl chloroglyoxylate; Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.61 (3H, s), 4.96 (2H, s), 7.11-7.17 (2H, m), 7.19-7.28 (4H, m), 7.28-7.34 (2H, m), 7.62-7.68 (2H, m), 7.78 (1H, brs), 7.80-7.87 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 617(4); Yield: 95% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.99 (2H, s), 7.11-7.18 (2H, m), 7.30-7.44 (6H, m), 7.81-7.98 (4H, m), 10.48 (1H, brs), 14.21 (1H, brs).
The intermediate 617(4) (372 mg, 0.703 mmol) was added to a suspension of sodium hydride (18.5 mg, 0.773 mmol) in N,N-dimethylformamide (5 ml) at 0° C., and the mixture was stirred for 30 minutes. Then iodomethane (0.087 ml, 1.41 mmol) was added to the mixture, and the mixture was stirred at room temperature for 1 hour. 2N hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (343 mg, 90%) as a white solid.
1H-NMR (CDCl3) δ: 1.28 (9H, s), 3.45 (3H, s), 3.47 (3H, s), 4.84 (2H, s), 6.87-6.95 (2H, m), 6.99-7.12 (6H, m), 7.20-7.29 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 618(1); Yield: 95% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 3.35 (3H, s), 4.83 (2H, s), 6.93-7.01 (2H, m), 7.04-7.12 (2H, m), 7.14-7.40 (8H, m), 13.97 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 4-(trifluoromethoxy)benzyl alcohol and 1,3-dinitrobenzene; Yield: 59% (yellow oil).
1H-NMR (CDCl3) δ: 5.14 (2H, s), 7.25-7.31 (3H, m), 7.46 (1H, t, J=8.1 Hz), 7.47-7.50 (2H, m), 7.82 (1H, t, J=2.4 Hz), 7.85-7.88 (1H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 619(1); Yield: 97% (pale brown solid).
1H-NMR (CDCl3) δ: 3.67 (2H, brs), 5.02 (2H, s), 6.29-6.41 (3H, m), 7.02-7.11 (1H, m), 7.19-7.25 (2H, m), 7.42-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 619(2) and methyl chloroglyoxylate; Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 3.98 (3H, s), 5.08 (2H, s), 6.80 (1H, ddd, J=0.9, 2.4, 8.4 Hz), 7.09 (1H, ddd, J=0.9, 2.4, 8.4 Hz), 7.20-7.27 (2H, m), 7.28 (1H, t, J=8.4 Hz), 7.45-7.51 (2H, m), 7.52 (1H, t, J=2.4 Hz), 8.83 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 619(3) and 4-(tert-butyl)benzyl bromide; Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 4.89 (2H, s), 4.92 (2H, s), 6.65 (1H, t, J=2.4 Hz), 6.71 (1H, ddd, J=0.9, 2.4, 7.8 Hz), 6.91 (1H, ddd, J=0.9, 2.4, 7.8 Hz), 7.12-7.18 (2H, m), 7.19-7.26 (3H, m), 7.28-7.34 (2H, m), 7.36-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 619(4); Yield: 80% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.91 (2H, s), 5.08 (2H, s), 6.78 (1H, ddd, J=0.9, 2.1, 7.8 Hz), 6.92 (1H, t, J=2.1 Hz), 6.97 (1H, ddd, J=0.9, 2.1, 8.1 Hz), 7.05-7.13 (2H, m), 7.25-7.35 (3H, m), 7.36-7.43 (2H, m), 7.51-7.59 (2H, m), 14.03 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 1-fluoro-2-nitrobenzene and 4-(trifluoromethoxy)benzyl alcohol; Yield: 80% (pale yellow solid).
1H-NMR (CDCl3) δ: 5.23 (2H, s), 7.03-7.14 (2H, m), 7.22-7.29 (2H, m), 7.48-7.57 (3H, m), 7.88 (1H, dd, J=1.5, 8.1 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 620(1); Yield: 100% (pale brown solid).
1H-NMR (CDCl3) δ: 3.82 (2H, brs), 5.08 (2H, s), 6.67-6.87 (4H, m), 7.20-7.27 (2H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 620(2) and methyl chloroglyoxylate; Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 3.96 (3H, s), 5.18 (2H, s), 6.96 (1H, dd, J=1.8, 7.8 Hz), 7.04 (1H, dt, J=1.8, 7.8 Hz), 7.13 (1H, dt, J=1.8, 7.8 Hz), 7.24-7.31 (2H, m), 7.45-7.51 (2H, m), 8.43 (1H, dd, J=1.5, 7.8 Hz), 9.56 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 620(3) and 4-(tert-butyl)benzyl bromide; Yield: 94% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (9H, s), 3.51 (3H, s), 4.52 (1H, d, J=14.4 Hz), 4.95 (1H, d, J=12.0 Hz), 5.03 (1H, d, J=12.0 Hz), 5.19 (1H, d, J=14.4 Hz), 6.83-7.00 (3H, m), 7.09-7.14 (2H, m), 7.19-7.30 (5H, m), 7.37-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 620(4); Yield: 88% (white solid).
1H-NMR (DMSO-d6) δ: 1.20 (9H, s), 4.43 (1H, d, J=15.0 Hz), 5.06 (1H, d, J=15.0 Hz), 5.13 (2H, s), 6.88 (1H, dt, J=0.9, 7.5 Hz), 7.01 (1H, dd, J=1.8, 7.8 Hz), 7.04-7.14 (3H, m), 7.18-7.32 (3H, m), 7.34-7.42 (2H, m), 7.51-7.57 (2H, m), 13.71 (1H, brs).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 1-fluoro-4-nitrobenzene and 4-(trifluoromethoxy)thiophenol; Yield: 92% (pale yellow oil).
1H-NMR (CDCl3) δ: 7.18-7.24 (2H, m), 7.27-7.32 (2H, m), 7.54-7.60 (2H, m), 8.08-8.13 (2H, m).
The title compound was obtained in the same manner as the Example 376(2) using the following starting material.
Starting material: the intermediate 621(1); Yield: 65% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.86 (2H, brs), 6.65-6.72 (2H, m), 7.01-7.13 (4H, m), 7.28-7.34 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 621(2) and methyl chloroglyoxylate; Yield: 92% (pale yellow solid).
1H-NMR (DMSO-d6) δ: 3.86 (3H, s), 7.29-7.38 (4H, m), 7.43-7.49 (2H, m), 7.80-7.86 (2H, m), 10.99 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 621(3) and 4-(tert-butyl)benzyl bromide; Yield: 98% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.58 (3H, s), 4.89 (2H, s), 6.97-7.04 (2H, m), 7.11-7.22 (6H, m), 7.28-7.33 (2H, m), 7.34-7.39 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 621(4); Yield: 83% (white solid).
1H-NMR (DMSO-d6) δ: 1.22 (9H, s), 4.88 (2H, s), 7.06-7.13 (2H, m), 7.17-7.24 (2H, m), 7.25-7.35 (4H, m), 7.35-7.46 (4H, m), 14.11 (1H, brs).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 4-nitrobenzcatechin and 4-(trifluoromethoxy)benzyl bromide; Yield: 92% (yellow solid).
1H-NMR (CDCl3) δ: 5.20 (2H, s), 5.24 (2H, s), 6.97 (1H, d, J=8.7 Hz), 7.23-7.26 (4H, m), 7.45-7.51 (4H, m), 7.84 (1H, d, J=2.4 Hz), 7.90 (1H, dd, J=2.4, 8.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 622(1); Yield: 68% (white solid).
1H-NMR (CDCl3) δ: 5.01 (2H, s), 5.07 (2H, s), 6.23 (1H, dd, J=2.7, 8.4 Hz), 6.34 (1H, d, J=2.7 Hz), 6.78 (1H, d, J=8.4 Hz), 7.16-7.26 (4H, m), 7.41-7.46 (4H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 622(2) and methyl chloroglyoxylate; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 3.97 (3H, s), 5.12 (2H, s), 5.16 (2H, s), 6.90 (1H, d, J=8.7 Hz), 6.99 (1H, dd, J=2.7, 8.7 Hz), 7.19-7.23 (4H, m), 7.42-7.50 (4H, m), 7.57 (1H, d, J=2.7 Hz), 8.76 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 622(3) and 4-(tert-butyl)benzyl bromide; Yield: 72% (yellow oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.48 (3H, s), 4.82 (2H, s), 4.91 (2H, s), 5.09 (2H, s), 6.57 (1H, d, J=2.4 Hz), 6.64 (1H, dd, J=2.4, 8.4 Hz), 6.80 (1H, d, J=8.4 Hz), 7.10-7.13 (2H, m), 7.21-7.22 (4H, m), 7.29-7.32 (2H, m), 7.34-7.37 (2H, m), 7.39-7.43 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 622(4); Yield: 39% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 3.48 (2H, s), 5.03 (2H, s), 5.07 (2H, s), 6.75-6.78 (1H, m), 6.90-6.93 (1H, m), 7.02-7.05 (2H, m), 7.20-7.27 (3H, m), 7.34-7.37 (4H, m), 7.51-7.54 (4H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 622(3) and iodomethane; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 3.28 (3H, s), 3.51 (3H, s), 5.11 (2H, s), 5.13 (2H, s), 6.76-6.83 (2H, m), 6.89 (1H, d, J=8.7 Hz), 7.21-7.24 (4H, m), 7.43-7.74 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 623(1); Yield: 79% (white solid).
1H-NMR (DMSO-d6) δ: 3.11 (3H, s), 5.11 (2H, s), 5.13 (2H, s), 6.85-6.87 (1H, m), 6.99-7.02 (1H, m), 7.14-7.16 (1H, m), 7.35-7.39 (4H, m), 7.54-7.60 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the compound 622 (3); Yield: 99% (white solid).
1H-NMR (DMSO-d6) δ: 5.10 (2H, s), 5.11 (2H, s), 6.98 (1H, d, J=9.0 Hz), 7.34-7.39 (5H, m), 7.53-7.64 (5H, m), 10.07 (1H, brs).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 2-methyl-5-nitrophenol and 4-(trifluoromethoxy)benzyl bromide; Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 2.36 (3H, s), 5.16 (2H, s), 7.22-7.32 (3H, m), 7.46-7.54 (2H, m), 7.70-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 625(1); Yield: 100% (gray solid).
1H-NMR (CDCl3) δ: 2.17 (3H, s), 3.55 (2H, brs), 5.02 (2H, s), 6.23-6.28 (2H, m), 6.90-6.97 (1H, m), 7.19-7.26 (2H, m), 7.43-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 625(2) and methyl chloroglyoxylate; Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 2.26 (3H, s), 3.98 (3H, s), 5.10 (2H, s), 6.91 (1H, dd, J=1.8, 7.8 Hz), 7.13 (1H, d, J=7.8 Hz), 7.20-7.27 (2H, m), 7.46-7.53 (2H, m), 7.55 (1H, d, J=1.8 Hz), 8.80 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 625(3) and 4-(tert-butyl)benzyl bromide; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 2.23 (3H, s), 3.53 (3H, s), 4.84 (2H, s), 4.86 (2H, s), 6.48 (1H, d, J=2.1 Hz), 6.62 (1H, dd, J=2.1, 7.5 Hz), 7.06 (1H, d, J=7.5 Hz), 7.11-7.17 (2H, m), 7.19-7.25 (2H, m), 7.28-7.34 (2H, m), 7.35-7.40 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 625(4); Yield: 97% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 2.14 (3H, s), 4.88 (2H, s), 5.06 (2H, s), 6.65 (1H, dd, J=1.8, 8.1 Hz), 6.94 (1H, d, J=1.5 Hz), 7.02-7.09 (2H, m), 7.11 (1H, d, J=8.1 Hz), 7.27-7.32 (2H, m), 7.36-7.43 (2H, m), 7.52-7.59 (2H, m), 13.12 (1H, brs).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-(trifluoromethoxy)aniline; Yield: 93% (brown oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.58 (3H, s), 4.86 (2H, s), 5.90 (1H, s), 6.85-6.99 (4H, m), 6.99-7.09 (2H, m), 7.09-7.22 (4H, m), 7.27-7.36 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 626(1); Yield: 84% (pale brown solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.62-4.90 (2H, m), 6.83-7.00 (2H, m), 7.00-7.38 (10H, m), 8.23-8.40 (1H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: 1-fluoro-4-nitrobenzene and 1-phenylpiperazine; Yield: 92% (yellow solid).
1H-NMR (CDCl3) δ: 3.31-3.42 (4H, m), 3.53-3.66 (4H, m), 6.81-7.03 (5H, m), 7.24-7.35 (2H, m), 8.11-8.20 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 627(1); Yield: 100% (gray solid).
1H-NMR (CDCl3) δ: 3.16-3.23 (4H, m), 3.31-3.37 (4H, m), 3.44 (2H, brs), 6.65-6.71 (2H, m), 6.84-6.92 (3H, m), 6.95-7.02 (2H, m), 7.27-7.33 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 627(2) and methyl chloroglyoxylate; Yield: 99% (yellow solid).
1H-NMR (CDCl3) δ: 3.34 (8H, brs), 3.97 (3H, s), 6.86-7.02 (5H, m), 7.26-7.34 (2H, m), 7.53-7.60 (2H, m), 8.76 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 627(3) and 4-(tert-butyl)benzyl bromide; Yield: 77% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.33 (8H, brs), 3.57 (3H, s), 4.85 (2H, s), 6.80-7.03 (7H, m), 7.13-7.19 (2H, m), 7.26-7.33 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 627(4); Yield: 94% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 3.19-3.35 (8H, m), 4.82 (2H, s), 6.77-7.08 (7H, m), 7.09-7.15 (2H, m), 7.19-7.27 (2H, m), 7.30-7.37 (2H, m), 13.80 (1H, brs).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: 1-fluoro-4-nitrobenzene and 1-[4-(trifluoromethoxy)phenyl]piperazine; Yield: 91% (yellow solid).
1H-NMR (CDCl3) δ: 3.31-3.38 (4H, m), 3.56-3.63 (4H, m), 6.85-6.97 (4H, m), 7.12-7.19 (2H, m), 8.13-8.19 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 628(1); Yield: 97% (pale brown solid).
1H-NMR (CDCl3) δ: 3.14-3.24 (4H, m), 3.29-3.37 (4H, m), 3.55 (2H, brs), 6.63-6.73 (2H, m), 6.84-7.00 (4H, m), 7.09-7.17 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 628(2) and methyl chloroglyoxylate; Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 3.22-3.34 (8H, m), 3.84 (3H, s), 6.97-7.03 (2H, m), 7.04-7.11 (2H, m), 7.19-7.26 (2H, m), 7.59-7.66 (2H, m), 10.64 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 628(3) and 4-(tert-butyl)benzyl bromide; Yield: 72% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.26-3.39 (8H, m), 3.57 (3H, s), 4.85 (2H, s), 6.80-6.87 (2H, m), 6.91-7.01 (4H, m), 7.11-7.20 (4H, m), 7.28-7.33 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 628(4); Yield: 95% (white solid).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 3.22-3.31 (8H, m), 4.81 (2H, s), 6.91-6.98 (2H, m), 7.00-7.15 (6H, m), 7.18-7.25 (2H, m), 7.31-7.37 (2H, m), 13.80 (1H, brs).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 2-chloro-5-nitrophenol and 4-(trifluoromethoxy)benzyl bromide; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 5.23 (2H, s), 7.24-7.31 (2H, m), 7.50-7.58 (3H, m), 7.80-7.87 (2H, m).
The title compound was obtained in the same manner as the Example 376(2) using the following starting material.
Starting material: the intermediate 629(1); Yield: 46% (pale brown solid).
1H-NMR (CDCl3) δ: 3.68 (2H, brs), 5.08 (2H, s), 6.26 (1H, dd, J=2.4, 8.1 Hz), 6.30 (1H, d, J=2.4 Hz), 7.13 (1H, d, J=8.1 Hz), 7.21-7.27 (2H, m), 7.46-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 629(2) and methyl chloroglyoxylate; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 3.99 (3H, s), 5.18 (2H, s), 6.94 (1H, dd, J=2.4, 8.4 Hz), 7.21-7.28 (2H, m), 7.36 (1H, d, J=8.4 Hz), 7.50-7.56 (2H, m), 7.72 (1H, d, J=2.4 Hz), 8.82 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 629(3) and 4-(tert-butyl)benzyl bromide; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.54 (3H, s), 4.85 (2H, s), 4.91 (2H, s), 6.57 (1H, d, J=2.1 Hz), 6.66 (1H, dd, J=2.1, 8.1 Hz), 7.09-7.14 (2H, m), 7.21-7.26 (2H, m), 7.29-7.35 (3H, m), 7.38-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 629(4); Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 1.23 (9H, s), 4.94 (2H, s), 5.19 (2H, s), 6.77 (1H, d, J=2.1, 8.1 Hz), 7.08 (1H, d, J=8.4 Hz), 7.24 (1H, d, J=2.1 Hz), 7.28-7.34 (2H, m), 7.38-7.47 (4H, m), 7.55-7.63 (2H, m), 14.02 (1H, brs).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 4-nitrothiophenol and 4-(trifluoromethoxy)benzyl bromide; Yield: 86% (pale yellow solid).
1H-NMR (CDCl3) δ: 4.24 (2H, s), 7.15-7.21 (2H, m), 7.30-7.35 (2H, m), 7.38-7.44 (2H, m), 8.09-8.14 (2H, m).
The title compound was obtained in the same manner as the Example 376(2) using the following starting material.
Starting material: the intermediate 630(1); Yield: 82% (white solid).
1H-NMR (CDCl3) δ: 3.76 (2H, brs), 3.90 (2H, s), 6.53-6.59 (2H, m), 7.05-7.19 (6H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 630(2) and methyl chloroglyoxylate; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 3.98 (3H, s), 4.07 (2H, s), 7.08-7.15 (2H, m), 7.24-7.32 (4H, m), 7.52-7.58 (2H, m), 8.82 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 630(3) and 4-(tert-butyl)benzyl bromide; Yield: 95% (colorless oil).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.53 (3H, s), 4.08 (2H, s), 4.87 (2H, s), 6.92-6.99 (2H, m), 7.09-7.15 (4H, m), 7.16-7.21 (2H, m), 7.23-7.32 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 630(4); Yield: 95% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.27 (2H, s), 4.86 (2H, s), 7.05-7.16 (4H, m), 7.24-7.36 (6H, m), 7.40-7.47 (2H, m), 13.99 (1H, brs).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 1-fluoro-2-nitrobenzene and 4-(trifluoromethoxy)thiophenol; Yield: 91% (yellow oil).
1H-NMR (CDCl3) δ: 6.86 (1H, dd, J=1.2, 8.1 Hz), 7.22-7.42 (4H, m), 7.59-7.66 (2H, m), 8.24 (1H, dd, J=1.5, 8.1 Hz).
The title compound was obtained in the same manner as the Example 376(2) using the following starting material.
Starting material: the intermediate 631(1); Yield: 79% (colorless oil).
1H-NMR (CDCl3) δ: 4.31 (2H, brs), 6.73-6.83 (2H, m), 7.02-7.12 (4H, m), 7.23-7.30 (1H, m), 7.45 (1H, dd, J=1.5, 7.5 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 631(2) and methyl chloroglyoxylate; Yield: 96% (colorless oil).
1H-NMR (CDCl3) δ: 3.93 (3H, s), 7.06-7.28 (5H, m), 7.47-7.55 (1H, m), 7.66 (1H, dd, J=1.8, 7.8 Hz), 8.53 (1H, dd, J=1.5, 8.1 Hz), 9.99 (1H, brs).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 631(3) and 4-(tert-butyl)benzyl bromide; Yield: 91% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 4.28 (1H, d, J=14.4 Hz), 5.48 (1H, d, J=14.4 Hz), 6.81-6.87 (1H, m), 7.05-7.25 (7H, m), 7.26-7.32 (2H, m), 7.40-7.46 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.55 (3H, s), 4.67 (1H, d, J=15.6 Hz), 4.91 (1H, d, J=15.0 Hz), 6.81-6.87 (1H, m), 7.05-7.25 (7H, m), 7.26-7.32 (2H, m), 7.40-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 631(4); Yield: 97% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.30 (1H, d, J=14.7 Hz), 5.28 (1H, d, J=14.7 Hz), 6.96-7.17 (4H, m), 7.18-7.50 (8H, m), 13.96 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.20 (9H, s), 4.74 (1H, d, J=15.3 Hz), 4.95 (1H, d, J=15.3 Hz), 6.96-7.17 (4H, m), 7.18-7.50 (8H, m), 13.96 (1H, brs).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: 2-aminobiphenyl and methyl chloroglyoxylate; Yield: 88% (pale purple solid).
1H-NMR (CDCl3) δ: 3.88 (3H, s), 7.22-7.55 (8H, m), 8.46 (1H, dd, J=2.1, 8.1 Hz), 9.08 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 632(1) and 4-bromobenzyl bromide; Yield: 100% (pale purple oil).
1H-NMR (CDCl3) δ: 3.38 (1H, d, J=14.7 Hz), 3.64 (3H, s), 5.10 (1H, d, J=14.7 Hz), 6.75-6.79 (1H, m), 6.86-6.91 (2H, m), 7.14-7.21 (1H, m), 7.28-7.33 (2H, m), 7.38-7.52 (5H, m), 7.57-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 632(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 52% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.49 (1H, d, J=14.1 Hz), 3.64 (3H, s), 5.20 (1H, d, J=14.1 Hz), 6.82-6.86 (1H, m), 7.08-7.12 (2H, m), 7.14-7.21 (1H, m), 7.23-7.29 (2H, m), 7.37-7.55 (9H, m), 7.59-7.64 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 632(3); Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 3.40 (1H, d, J=14.7 Hz), 5.01 (1H, d, J=14.7 Hz), 6.97-7.00 (1H, m), 7.08 (2H, d, J=8.4 Hz), 7.27-7.34 (1H, m), 7.38-7.58 (9H, m), 7.66-7.69 (2H, m), 7.71-7.75 (2H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 354(1) and ethyl 7-bromoheptanoate; Yield: 70% (yellow solid).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.41-1.46 (2H, m), 1.49-1.56 (2H, m), 1.62-1.68 (2H, m), 1.70-1.92 (2H, m), 2.32 (2H, t, J=7.2 Hz), 4.10-4.67 (4H, m), 6.97-7.00 (2H, m), 7.04-7.08 (2H, m), 7.18-7.22 (2H, m), 7.50 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 633(1); Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.36-1.56 (4H, m), 1.62-1.68 (2H, m), 1.70-1.90 (2H, m), 2.32 (2H, t, J=7.2 Hz), 3.89 (2H, brs), 4.03 (2H, t, J=6.6 Hz), 4.13 (2H, q, J=7.2 Hz), 6.86 (1H, d, J=8.1 Hz), 6.90-6.92 (2H, m), 7.21-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 633(2) and 4-phenylbutyl bromide; Yield: 42% (colorless oil).
1H-NMR (CDCl3) δ: 1.26 (3H, t, J=7.2 Hz), 1.42-1.90 (12H, m), 2.32 (2H, t, J=7.2 Hz), 2.66-2.69 (2H, m), 3.19-3.22 (2H, m), 3.99-4.04 (2H, m), 4.10-4.14 (2H, m), 4.26 (1H, brs), 6.73-6.79 (3H, m), 7.18-7.30 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 633(3) and methyl chloroglyoxylate; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.2 Hz), 1.38-1.82 (12H, m), 2.31 (2H, t, J=7.2 Hz), 2.56-2.67 (2H, m), 3.48-3.54 (4H, m), 3.99-4.04 (3H, m), 4.13 (2H, q, J=7.2 Hz), 6.98 (1H, d, J=8.7 Hz), 7.10-7.15 (3H, m), 7.19-7.29 (4H, m), 7.32 (1H, d, J=2.4 Hz), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 633(4); Yield: 18% (colorless oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.30-1.59 (10H, m), 1.66-1.70 (2H, m), 2.20 (2H, t, J=7.5 Hz), 2.49-2.57 (2H, m), 3.40-3.53 (1H, m), 3.85-3.91 (1H, m), 3.96-4.10 (2H, m), 7.10-7.13 (3H, m), 7.17-7.21 (3H, m), 7.43-7.48 (3H, m), 7.65-7.71 (3H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.30-1.59 (10H, m), 1.66-1.70 (2H, m), 2.20 (2H, t, J=7.5 Hz), 2.49-2.57 (2H, m), 3.57-3.65 (1H, m), 3.96-4.10 (3H, m), 7.08-7.13 (3H, m), 7.17-7.22 (3H, m), 7.43-7.48 (3H, m), 7.68-7.76 (3H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 2-adamantanol; Yield: 74% (yellow solid).
1H-NMR (CDCl3) δ: 1.52-1.59 (2H, m), 1.77-1.82 (4H, m), 1.90-1.98 (4H, m), 2.15-2.23 (4H, m), 4.63-4.65 (1H, m), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.59 (2H, m), 7.70 (1H, dd, J=2.4, 8.7 Hz), 8.02 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 634(1); Yield: 66% (white solid).
1H-NMR (CDCl3) δ: 1.52-1.59 (2H, m), 1.77-1.82 (4H, m), 1.90-1.98 (4H, m), 2.15-2.23 (4H, m), 3.94 (2H, brs), 4.47-4.49 (1H, m), 6.83 (1H, d, J=8.4 Hz), 6.87 (1H, dd, J=2.1, 8.4 Hz), 6.94 (1H, d, J=2.1 Hz), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 634(2) and 4-phenylbutyl bromide; Yield: 83% (white solid).
1H-NMR (CDCl3) δ: 1.52-1.59 (2H, m), 1.70-1.98 (12H, m), 2.15-2.23 (4H, m), 2.65-2.72 (2H, m), 3.19-3.27 (2H, m), 4.38 (1H, brs), 4.47-4.49 (1H, m), 6.76-6.78 (3H, m), 7.10-7.31 (7H, m), 7.52-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 634(3) and methyl chloroglyoxylate; Yield: 81% (colorless oil).
1H-NMR (CDCl3) δ: 1.52-1.98 (14H, m), 2.15-2.23 (4H, m), 2.57-2.64 (2H, m), 3.43-3.53 (4H, m), 4.16-4.24 (1H, m), 4.46-4.48 (1H, m), 6.96 (1H, d, J=8.7 Hz), 7.10-7.15 (3H, m), 7.19-7.23 (4H, m), 7.31 (1H, d, J=2.4 Hz), 7.44-7.49 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 634(4); Yield: 70% (yellow oil).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.37-1.50 (6H, m), 1.70-1.91 (8H, m), 2.06-2.21 (4H, m), 2.44-2.50 (2H, m), 3.22-3.26 (1H, m), 4.09-4.12 (1H, m), 4.53-4.56 (1H, m), 7.06-7.20 (6H, m), 7.40-7.43 (3H, m), 7.49-7.52 (1H, m), 7.62-7.65 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.37-1.50 (6H, m), 1.70-1.91 (8H, m), 2.06-2.21 (4H, m), 2.44-2.50 (2H, m), 3.22-3.26 (1H, m), 3.66-3.68 (1H, m), 4.53-4.56 (1H, m), 7.02-7.20 (5H, m), 7.30 (1H, d, J=2.4 Hz), 7.40-7.51 (4H, m), 7.64-7.70 (2H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: 4-bromo-2-fluoro-1-nitrobenzene and 4-(tert-butyl)phenol; Yield: 100% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 6.97-7.02 (2H, m), 7.12 (1H, d, J=1.8 Hz), 7.28 (1H, dd, J=1.8, 8.7 Hz), 7.40-7.44 (2H, m), 7.83 (1H, d, J=8.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 635(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 76% (yellow oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 7.00-7.04 (2H, m), 7.18 (1H, d, J=1.8 Hz), 7.26-7.30 (2H, m), 7.34 (1H, dd, J=1.8, 8.4 Hz), 7.38-7.42 (2H, m), 7.49-7.53 (2H, m), 8.05 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 635(2); Yield: 52% (gray solid).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 3.91 (2H, brs), 6.88 (1H, d, J=8.1 Hz), 6.91-6.97 (2H, m), 7.11 (1H, d, J=2.1 Hz), 7.17-7.22 (3H, m), 7.30-7.36 (2H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 635(3) and 4-phenylbutyl bromide; Yield: 45% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.31 (9H, s), 1.62-2.05 (4H, m), 2.64 (2H, d, J=7.2 Hz), 3.14-3.25 (2H, m), 4.26 (1H, brs), 6.76 (1H, d, J=8.4 Hz), 6.91-6.96 (2H, m), 7.07 (1H, d, J=2.1 Hz), 7.14-7.35 (10H, m), 7.43-7.49 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 635(4) and methyl chloroglyoxylate; Yield: 63% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.65-1.68 (4H, m), 2.58-2.62 (2H, m), 3.63 (3H, s), 3.64-3.70 (1H, m), 3.99-4.04 (1H, m), 6.94-7.00 (2H, m), 7.05 (1H, d, J=2.1 Hz), 6.99-7.29 (9H, m), 7.34-7.40 (2H, m), 7.44-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 635(5); Yield: 85% (white solid).
1H-NMR (DMSO-d6) δ: 1.28 (9H, s), 1.45-1.60 (4H, m), 2.49-2.54 (2H, m), 3.48-3.95 (2H, m), 6.95-7.26 (8H, m), 7.38-7.47 (6H, m), 7.65-7.73 (2H, m).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: the intermediate 188(1) and 4-(tert-butyl)phenol; Yield: 100% (whitish-pink solid).
1H-NMR (CDCl3) δ: 1.34 (9H, s), 7.01-7.04 (2H, m), 7.08 (1H, d, J=8.4 Hz), 7.30-7.34 (2H, m), 7.40-7.43 (2H, m), 7.56-7.59 (2H, m), 7.65 (1H, dd, J=2.4, 8.4 Hz), 8.13 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 636(1); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 3.91 (2H, brs), 6.85-7.00 (5H, m), 7.24-7.26 (2H, m), 7.33-7.36 (2H, m), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 636(2) and 4-phenylbutyl bromide; Yield: 57% (colorless oil).
1H-NMR (CDCl3) δ: 1.32 (9H, s), 1.66-1.90 (4H, m), 2.62-2.67 (2H, m), 3.21-3.23 (2H, m), 4.22-4.28 (1H, m), 6.74-6.87 (3H, m), 6.93-6.97 (2H, m), 7.14-7.35 (9H, m), 7.54-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 636(3) and methyl chloroglyoxylate; Yield: 42% (colorless oil).
1H-NMR (CDCl3) δ: 1.33 (9H, s), 1.66-1.70 (4H, m), 2.59-2.62 (2H, m), 3.60-3.71 (4H, m), 4.02-4.10 (1H, m), 6.92 (1H, d, J=8.4 Hz), 6.95-6.99 (2H, m), 7.08-7.24 (5H, m), 7.27-7.30 (2H, m), 7.37-7.44 (4H, m), 7.48-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 636(4); Yield: 84% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 1.48-1.54 (4H, m), 2.44-2.50 (2H, m), 3.15-3.26 (2H, m), 6.82 (1H, d, J=8.4 Hz), 7.08-7.20 (7H, m), 7.37-7.52 (6H, m), 7.62-7.69 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.29 (9H, s), 1.48-1.54 (4H, m), 2.44-2.50 (2H, m), 3.15-3.26 (1H, m), 3.64-3.68 (1H, m), 6.87 (1H, d, J=8.4 Hz), 6.94-6.97 (2H, m), 7.08-7.20 (5H, m), 7.37-7.55 (6H, m), 7.62-7.75 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 4-(butyl)cyclohexanol; Yield: 98% (pale brown oil).
This compound was obtained as a mixture of the geometric isomers (2:1).
Major isomer: 1H-NMR (CDCl3) δ: 0.82-1.64 (15H, m), 1.80-2.23 (3H, m), 4.26-4.39 (1H, m), 7.17 (1H, d, J=6.0 Hz), 7.27-7.32 (2H, m), 7.52-7.58 (2H, m), 7.66 (1H, dd, J=2.7, 8.7 Hz), 7.99 (1H, d, J=2.7 Hz).
Minor isomer: 1H-NMR (CDCl3) δ: 0.82-1.64 (15H, m), 1.80-2.23 (3H, m), 4.71-4.78 (1H, m), 7.14 (1H, d, J=6.0 Hz), 7.27-7.32 (2H, m), 7.52-7.58 (2H, m), 7.66 (1H, dd, J=2.7, 8.7 Hz), 8.01 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 637(1); Yield: 86% (white solid).
This compound was obtained as a mixture of the geometric isomers (3:1).
Major isomer: 1H-NMR (CDCl3) δ: 0.84-1.66 (15H, m), 1.80-2.25 (3H, m), 3.87 (2H, brs), 4.10-4.23 (1H, m), 6.82-6.96 (3H, m), 7.19-7.25 (2H, m), 7.48-7.55 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.84-1.66 (15H, m), 1.80-2.25 (3H, m), 3.87 (2H, brs), 4.61-4.64 (1H, m), 6.82-6.96 (3H, m), 7.19-7.25 (2H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 637(2) and 4-phenylbutyl bromide; Yield: 43% (colorless oil).
This compound was obtained as a mixture of the geometric isomers (3:1).
Major isomer: 1H-NMR (CDCl3) δ: 0.83-2.24 (22H, m), 2.55-2.73 (2H, m), 3.09-3.28 (2H, m), 4.08-4.20 (1H, m), 4.24-4.32 (1H, m), 6.71-6.86 (3H, m), 7.10-7.34 (7H, m), 7.50-7.58 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.83-2.24 (22H, m), 2.55-2.73 (2H, m), 3.09-3.28 (2H, m), 4.29-4.35 (1H, m), 4.53-4.60 (1H, m), 6.71-6.86 (3H, m), 7.10-7.34 (7H, m), 7.50-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 637(3) and methyl chloroglyoxylate; Yield: 66% (colorless oil).
This compound was obtained as a mixture of the geometric isomers (3:1).
Major isomer: 1H-NMR (CDCl3) δ: 0.83-2.18 (22H, m), 2.54-2.65 (2H, m), 3.45-3.62 (1H, m), 3.53 (3H, s), 3.87-4.02 (1H, m), 4.13-4.28 (1H, m), 6.98 (1H, d, J=8.7 Hz), 7.08-7.30 (8H, m), 7.31 (1H, d, J=2.4 Hz), 7.44-7.52 (2H, m).
Minor isomer: 1H-NMR (CDCl3) δ: 0.83-2.18 (22H, m), 2.54-2.65 (2H, m), 3.45-3.62 (1H, m), 3.52 (3H, s), 4.07-4.21 (1H, m), 4.55-4.62 (1H, m), 6.97 (1H, d, J=8.7 Hz), 7.08-7.31 (9H, m), 7.44-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 637(4); Yield: 68% (white solid).
This compound was obtained as a mixture of the geometric isomers (3:1).
Major isomer: 1H-NMR (DMSO-d6) δ: 0.80-2.04 (22H, m), 2.44-2.59 (2H, m), 3.43-3.58 (1H, m), 3.74-3.86 (1H, m), 4.26-4.40 (1H, m), 7.04-7.24 (6H, m), 7.38-7.47 (3H, m), 7.57-7.72 (3H, m), 13.49 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.80-2.04 (22H, m), 2.44-2.59 (2H, m), 3.43-3.58 (1H, m), 3.87-3.99 (1H, m), 4.62-4.69 (1H, m), 7.04-7.24 (6H, m), 7.38-7.47 (3H, m), 7.57-7.72 (3H, m), 13.49 (1H, brs).
The title compound was obtained in the same manner as the Example 132(1) using the following starting materials.
Starting materials: the intermediate 188(1) and phenol; Yield: 92% (brown solid).
1H-NMR (CDCl3) δ: 7.05-7.15 (3H, m), 7.18-7.26 (1H, m), 7.28-7.37 (2H, m), 7.37-7.46 (2H, m), 7.55-7.63 (2H, m), 7.67 (1H, dd, J=2.4, 8.4 Hz), 8.14 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 638(1); Yield: 91% (pale yellow oil).
1H-NMR (CDCl3) δ: 3.91 (2H, s), 6.84-6.96 (2H, m), 6.98-7.14 (4H, m), 7.21-7.30 (2H, m), 7.30-7.39 (2H, m), 7.51-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 638(2) and 4-phenylbutyl bromide; Yield: 49% (yellow oil).
1H-NMR (CDCl3) δ: 1.60-1.79 (4H, m), 2.57-2.72 (2H, m), 3.14-3.28 (2H, m), 4.17-4.26 (1H, m), 6.77 (1H, dd, J=2.7, 8.4 Hz), 6.82-6.91 (2H, m), 6.98-7.38 (12H, m), 7.52-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 638(3) and methyl chloroglyoxylate; Yield: 73% (colorless oil).
1H-NMR (CDCl3) δ: 1.58-1.75 (4H, m), 2.50-2.70 (2H, m), 3.54-3.73 (4H, m), 3.97-4.13 (1H, m), 6.92 (1H, d, J=8.4 Hz), 7.01-7.34 (10H, m), 7.34-7.46 (4H, m), 7.46-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 638(4); Yield: 94% (white solid).
1H-NMR (CDCl3) δ: 1.28-1.60 (4H, m), 2.24-2.47 (2H, m), 3.30-3.54 (1H, m), 3.56-3.80 (1H, m), 6.58-7.50 (17H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and l-menthol; Yield: 66% (brown oil).
1H-NMR (CDCl3) δ: 0.77 (3H, d, J=6.9 Hz), 0.83-1.36 (9H, m), 1.42-1.84 (4H, m), 2.12-2.32 (2H, m), 4.25 (1H, td, J=3.9, 10.5 Hz), 7.16 (1H, d, J=8.7 Hz), 7.24-7.35 (2H, m), 7.50-7.61 (2H, m), 7.66 (1H, dd, J=2.7, 8.7 Hz), 7.97 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 639(1); Yield: 91% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.75-1.36 (11H, m), 1.36-1.64 (3H, m), 1.67-1.82 (2H, m), 2.14-2.33 (2H, m), 3.88 (2H, s), 4.02-4.20 (1H, m), 6.80-6.97 (3H, m), 7.16-7.30 (2H, m), 7.46-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 639(2) and 4-phenylbutyl bromide; Yield: 59% (brown oil).
1H-NMR (CDCl3) δ: 0.70-1.30 (11H, m), 1.36-1.65 (3H, m), 1.65-1.95 (6H, m), 2.08-2.28 (2H, m), 2.53-2.74 (2H, m), 3.02-3.32 (2H, m), 4.02-4.16 (1H, m), 4.24-4.38 (1H, m), 6.72-6.86 (2H, m), 7.05-7.35 (8H, m), 7.46-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 639(3) and methyl chloroglyoxylate; Yield: 72% (colorless oil).
1H-NMR (CDCl3) δ: 0.71-0.86 (2H, m), 0.86-1.32 (9H, m), 1.32-1.88 (9H, m), 2.00-2.30 (2H, m), 2.48-2.72 (2H, m), 3.30-3.45 (1H, m), 3.45-3.64 (3H, m), 4.05-4.29 (2H, m), 6.98-7.07 (1H, m), 7.07-7.17 (3H, m), 7.17-7.39 (5H, m), 7.43-7.57 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 639(4); Yield: 55% (white solid).
1H-NMR (CDCl3) δ: 0.48-1.18 (12H, m), 1.30-1.82 (8H, m), 1.90-2.20 (2H, m), 2.36-2.68 (2H, m), 3.42-3.64 (1H, m), 3.74-3.96 (1H, m), 4.00-4.20 (1H, m), 6.86-7.32 (9H, m), 7.32-7.58 (3H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 226(1) and ethyl bromoacetate; Yield: 56% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.21 (3H, t, J=6.9 Hz), 1.30-1.87 (10H, m), 2.58-2.64 (2H, m), 3.31-3.36 (2H, m), 3.99 (2H, t, J=6.6 Hz), 4.04 (2H, s), 4.11 (2H, t, J=7.2 Hz), 6.88 (1H, d, J=8.4 Hz), 7.09 (1H, dd, J=2.4, 8.4 Hz), 7.11-7.16 (3H, m), 7.17 (1H, d, J=2.4 Hz), 7.21-7.28 (4H, m), 7.47-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 640(1); Yield: 60% (colorless oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.9 Hz), 1.33-1.71 (8H, m), 1.80-1.88 (2H, m), 2.59 (2H, t, J=7.5 Hz), 3.13 (2H, t, J=7.2 Hz), 3.64 (2H, s), 4.04 (2H, t, J=6.9 Hz), 6.97 (1H, d, J=8.4 Hz), 7.08-7.32 (9H, m), 7.45-7.51 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 3-bromoaniline and ethyl 2-bromohexanoate; Yield: 48% (colorless oil).
1H-NMR (CDCl3) δ: 0.88-0.94 (3H, m), 1.24-1.36 (7H, m), 1.70-1.82 (2H, m), 3.99-4.25 (4H, m), 6.50-6.55 (1H, m), 6.75 (1H, t, J=1.8 Hz), 6.81-6.86 (1H, m), 7.01 (1H, t, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 641(1) and 4-(tert-butyl)benzyl bromide; Yield: 57% (colorless oil).
1H-NMR (CDCl3) δ: 0.82 (3H, t, J=7.2 Hz), 1.19-1.37 (16H, m), 1.71-2.12 (2H, m), 4.11 (2H, q, J=7.2 Hz), 4.30-4.33 (1H, m), 4.49-4.62 (2H, m), 6.65-6.68 (1H, m), 6.83-6.86 (1H, m), 6.95 (1H, t, J=2.4 Hz), 6.99 (1H, t, J=8.4 Hz), 7.16-7.29 (2H, m), 7.29-7.32 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 641(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 73% (yellow oil).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=7.2 Hz), 1.19-1.37 (16H, m), 1.71-2.12 (2H, m), 4.13 (2H, q, J=7.2 Hz), 4.30-4.33 (1H, m), 4.49-4.62 (2H, m), 6.78-6.83 (1H, m), 6.89-6.94 (2H, m), 7.19-7.34 (7H, m), 7.40-7.45 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 641(3); Yield: 81% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.78 (3H, t, J=7.2 Hz), 1.11-1.40 (13H, m), 1.74-1.98 (2H, m), 4.44-4.62 (3H, m), 6.70-6.75 (1H, m), 6.89-6.94 (2H, m), 7.17-7.27 (3H, m), 7.31-7.36 (2H, m), 7.37-7.40 (2H, m), 7.57-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: 4-bromoaniline and ethyl 2-bromohexanoate; Yield: 36% (yellow oil).
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.2 Hz), 1.25 (3H, t, J=7.2 Hz), 1.33-1.41 (4H, m), 1.71-1.81 (2H, m), 3.97-4.01 (1H, m), 4.10-4.22 (3H, m), 6.48-6.51 (2H, m), 7.22-7.26 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 642(1) and 4-(tert-butyl)benzyl bromide; Yield: 72% (colorless oil).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=7.2 Hz), 1.21 (3H, t, J=7.2 Hz), 1.25-1.36 (13H, m), 1.75-2.00 (2H, m), 4.11 (2H, q, J=7.2 Hz), 4.31 (1H, t, J=7.2 Hz), 4.43-4.63 (2H, m), 6.63-6.67 (2H, m), 7.15-7.31 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 642(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 85% (yellow oil).
1H-NMR (CDCl3) δ: 0.83 (3H, t, J=7.2 Hz), 1.22-1.43 (16H, m), 1.78-1.90 (1H, m), 1.95-2.07 (1H, m), 4.08-4.18 (2H, m), 4.43 (1H, t, J=7.5 Hz), 4.52-4.72 (2H, m), 6.83-6.86 (2H, m), 7.19-7.26 (4H, m), 7.31-7.40 (4H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 642(3); Yield: 34% (yellowish-white solid).
1H-NMR (DMSO-d6) δ: 0.79 (3H, t, J=7.2 Hz), 1.15-1.40 (13H, m), 1.74-1.78 (1H, m), 1.90-1.96 (1H, m), 4.48-4.53 (3H, m), 6.80-6.83 (2H, m), 7.22-7.25 (2H, m), 7.31-7.36 (4H, m), 7.45-7.48 (2H, m), 7.64-7.67 (2H, m), 12.72 (1H, s).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 367(4) and ethyl bromoacetate; Yield: 77% (pale brown oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.23 (3H, t, J=7.2 Hz), 1.34-1.49 (4H, m), 1.58-1.72 (4H, m), 1.82 (2H, quint, J=6.9 Hz), 2.62 (2H, t, J=7.2 Hz), 3.32 (2H, t, J=6.9 Hz), 4.01 (2H, t, J=6.6 Hz), 4.06 (2H, s), 4.13 (2H, q, J=7.2 Hz), 7.00-7.28 (10H, m), 7.51-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 643(1); Yield: 82% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.6 Hz), 1.34-1.95 (10H, m), 2.60 (2H, t, J=7.2 Hz), 3.13 (2H, t, J=7.5 Hz), 3.65 (2H, s), 4.06 (2H, t, J=6.6 Hz), 7.05-7.30 (10H, m), 7.51-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 351(3) and ethyl bromoacetate; Yield: 58% (white solid).
1H-NMR (CDCl3) δ: 1.19 (3H, t, J=7.2 Hz), 1.23 (9H, s), 1.58-1.76 (4H, m), 2.61 (2H, t, J=6.9 Hz), 3.40 (2H, t, J=6.9 Hz), 3.72 (2H, t, J=5.7 Hz), 4.09 (2H, t, J=7.2 Hz), 4.13 (2H, t, J=5.7 Hz), 4.13 (2H, s), 6.91 (1H, d, J=8.4 Hz), 7.07-7.62 (11H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 644(1); Yield: 46% (colorless oil).
1H-NMR (CDCl3) δ: 1.22 (9H, s), 1.53-1.71 (4H, m), 2.59 (2H, t, J=7.2 Hz), 3.15 (2H, t, J=7.5 Hz), 3.71 (2H, s), 3.72 (2H, t, J=5.4 Hz), 4.14 (2H, t, J=5.1 Hz), 6.98 (1H, d, J=8.1 Hz), 7.10-7.52 (11H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 5-bromosalicylaldehyde and 4-(trifluoromethoxy)phenylboronic acid; Yield: 78% (yellow solid).
1H-NMR (CDCl3) δ: 7.09 (1H, d, J=8.1 Hz), 7.30 (2H, d, J=7.8 Hz), 7.54-7.59 (2H, m), 7.72-7.76 (2H, m), 9.98 (1H, s), 11.03 (1H, s).
The title compound was obtained in the same manner as the Example 354(2) using the following starting material.
Starting material: the intermediate 645(1); Yield: 83% (colorless oil).
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.37-1.55 (4H, m), 1.83-1.91 (2H, m), 4.13 (2H, t, J=6.3 Hz), 7.06 (1H, d, J=8.4 Hz), 7.25-7.29 (2H, m), 7.55-7.59 (2H, m), 7.73 (1H, dd, J=2.4, 8.4 Hz), 8.04 (1H, d, J=2.4 Hz), 10.55 (1H, s).
A mixture of the intermediate 645(2) (875 mg, 2.484 mmol), 4-(tert-butyl)aniline (408 mg, 2.732 mmol), sodium triacetoxyborohydride (790 mg, 3.726 mmol), acetic acid (164 mg, 2.732 mmol) and dichloromethane (7 ml) was stirred at room temperature for 4 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=15:1) to give the title compound (1.21 g, 100%) as a colorless oil.
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.27 (9H, s), 1.35-1.51 (4H, m), 1.80-1.86 (2H, m), 4.05 (2H, t, J=6.3 Hz), 4.11 (1H, s), 4.38 (2H, s), 6.61-6.67 (2H, m), 6.93 (1H, d, J=8.4 Hz), 7.17-7.26 (4H, m), 7.40 (1H, dd, J=2.4, 8.4 Hz), 7.47-7.52 (2H, m), 7.53 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 645(3) and methyl chloroglyoxylate; Yield: 89% (pale brown oil).
1H-NMR (CDCl3) δ: 0.86-0.96 (3H, m), 1.22-1.41 (13H, m), 1.55-1.68 (2H, m), 3.54 (3H, s), 3.82 (2H, t, J=6.6 Hz), 5.04 (2H, s), 6.84 (1H, d, J=8.4 Hz), 6.99-7.08 (2H, m), 7.18-7.33 (4H, m), 7.40 (1H, dd, J=2.4, 8.4 Hz), 7.45-7.55 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 645(4); Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 0.83-0.94 (3H, m), 1.14-1.46 (13H, m), 1.58-1.73 (2H, m), 3.80-4.07 (2H, m), 4.79 (2H, s), 6.90-7.08 (1H, m), 7.08-7.35 (4H, m), 7.35-7.56 (3H, m), 7.56-7.77 (3H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 354(1) and ethyl 9-bromononanoate; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 1.23-1.28 (3H, m), 1.30-1.36 (6H, m), 1.48-1.52 (2H, m), 1.60-1.65 (2H, m), 1.80-1.85 (2H, m), 2.26-2.32 (2H, m), 4.10-4.14 (4H, m), 7.16 (1H, d, J=8.7 Hz), 7.28-7.33 (2H, m), 7.54-7.58 (2H, m), 7.77 (1H, dd, J=2.7, 8.7 Hz), 8.02 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 646(1); Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 1.23-1.28 (3H, m), 1.30-1.36 (6H, m), 1.48-1.52 (2H, m), 1.60-1.65 (2H, m), 1.80-1.85 (2H, m), 2.26-2.32 (2H, m), 3.89 (2H, brs), 4.03 (2H, t, J=6.6 Hz), 4.12 (2H, q, J=7.2 Hz), 6.83 (1H, d, J=8.4 Hz), 6.88-6.94 (2H, m), 7.21-7.24 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 646(2) and 4-phenylbutyl bromide; Yield: 67% (colorless oil).
1H-NMR (CDCl3) δ: 1.23-1.28 (3H, m), 1.30-1.85 (16H, m), 2.26-2.32 (2H, m), 2.68 (2H, t, J=7.2 Hz), 3.18-3.24 (2H, m), 4.03 (2H, t, J=6.6 Hz), 4.12 (2H, q, J=7.2 Hz), 4.25-4.29 (1H, m), 6.73-6.80 (3H, m), 7.18-7.30 (7H, m), 7.52-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 646(3) and methyl chloroglyoxylate; Yield: 78% (colorless oil).
1H-NMR (CDCl3) δ: 1.23-1.28 (3H, m), 1.30-1.85 (16H, m), 2.29 (2H, t, J=7.2 Hz), 2.57-2.63 (2H, m), 3.48-3.58 (4H, m), 3.97-4.09 (3H, m), 4.12 (2H, q, J=7.2 Hz), 6.98 (1H, d, J=8.4 Hz), 7.10-7.15 (3H, m), 7.19-7.28 (4H, m), 7.31 (1H, d, J=2.4 Hz), 7.46-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 646(4); Yield: 29% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.27-1.54 (14H, m), 1.67-1.74 (2H, m), 2.10-2.16 (2H, m), 2.48-2.51 (2H, m), 3.19-4.01 (4H, m), 7.07-7.20 (6H, m), 7.40-7.43 (2H, m), 7.48-7.54 (2H, m), 7.64-7.67 (2H, m), 12.52 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.27-1.54 (14H, m), 1.67-1.74 (2H, m), 2.10-2.16 (2H, m), 2.48-2.51 (2H, m), 3.19-4.01 (4H, m), 7.07-7.20 (5H, m), 7.30 (1H, d, J=2.1 Hz), 7.40-7.43 (2H, m), 7.48-7.59 (2H, m), 7.68-7.71 (2H, m), 12.52 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 645(3) and ethyl bromoacetate; Yield: 51% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.6 Hz), 1.24 (3H, t, J=7.2 Hz), 1.26 (9H, s), 1.30-1.59 (4H, m), 1.76-1.89 (2H, m), 4.03 (2H, t, J=6.6 Hz), 4.12 (2H, s), 4.21 (2H, q, J=7.2 Hz), 4.66 (2H, s), 6.58-6.69 (2H, m), 6.93 (1H, d, J=8.1 Hz), 7.13-7.27 (4H, m), 7.40 (1H, dd, J=2.4, 8.1 Hz), 7.43-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 647(1); Yield: 87% (white solid).
1H-NMR (DMSO-d6) δ: 0.91 (3H, t, J=7.2 Hz), 1.16 (9H, s), 1.28-1.53 (4H, m), 1.70-1.85 (2H, m), 3.85 (2H, s), 4.08 (2H, t, J=6.3 Hz), 4.51 (2H, s), 6.40 (2H, d, J=8.7 Hz), 6.98-7.14 (3H, m), 7.32 (2H, d, J=8.7 Hz), 7.50 (1H, dd, J=2.4, 8.4 Hz), 7.60-7.72 (2H, m), 7.79 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 4-bromo-2-hydroxybenzonitrile and 1-chloropentane; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.36-1.53 (4H, m), 1.86 (2H, quint, J=6.6 Hz), 4.06 (2H, t, J=6.6 Hz), 7.11-7.15 (2H, m), 7.40 (1H, d, J=7.8 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 648(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 95% (white solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=6.9 Hz), 1.35-1.56 (4H, m), 1.89 (2H, quint, J=6.3 Hz), 4.14 (2H, t, J=6.3 Hz), 7.09-7.17 (2H, m), 7.32 (2H, d, J=8.4 Hz), 7.58-7.61 (3H, m).
A solution of the intermediate 648(2) (500 mg, 1.43 mmol) in anhydrous tetrahydrofuran (2 ml) was added dropwise to a suspension of lithium aluminium hydride (163 mg, 4.29 mmol) in anhydrous tetrahydrofuran (3 ml) under reflux, and the mixture was stirred for 40 minutes. The reaction mixture was cooled to 0° C., followed by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (520 mg, 100%) as a pale brown oil.
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.5 Hz), 1.34-1.54 (4H, m), 1.81-1.90 (4H, m), 3.87 (2H, s), 4.06 (2H, t, J=6.6 Hz), 7.01 (1H, d, J=1.8 Hz), 7.08 (1H, dd, J=1.8, 7.5 Hz), 7.26-7.30 (3H, m), 7.55-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 157(2) using the following starting materials.
Starting materials: the intermediate 648(3) and 1-bromo-4-(tert-butyl)benzene; Yield: 42% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.5 Hz), 1.27 (9H, s), 1.30-1.53 (4H, m), 1.78-1.92 (3H, m), 4.07 (2H, t, J=6.6 Hz), 4.37 (2H, s), 6.06-6.65 (2H, m), 7.02-7.40 (7H, m), 7.47-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 648(4) and methyl chloroglyoxylate; Yield: 69% (colorless oil).
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=6.9 Hz), 1.27 (9H, s), 1.31-1.39 (4H, m), 1.56-1.70 (2H, m), 3.54 (3H, s), 3.84 (2H, t, J=6.6 Hz), 5.03 (2H, s), 6.93 (1H, d, J=1.8 Hz), 7.04-7.11 (3H, m), 7.25-7.32 (4H, m), 7.42 (1H, d, J=8.1 Hz), 7.54-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 648(5); Yield: 89% (solid).
1H-NMR (DMSO-d6) δ: 0.87 (3H, t, J=6.9 Hz), 1.23 (9H, s), 1.26-1.35 (4H, m), 1.52-1.70 (2H, m), 3.95 (2H, t, J=6.3 Hz), 4.85 (2H, s), 7.16-7.23 (4H, m), 7.32-7.36 (3H, m), 7.43 (2H, d, J=8.4 Hz), 7.79 (2H, d, J=8.4 Hz), 14.01 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 648(4) and ethyl bromoacetate; Yield: 70% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=6.9 Hz), 1.23 (3H, t, J=6.6 Hz), 1.27 (9H, s), 1.34-1.50 (4H, m), 1.84 (2H, quint, J=6.9 Hz), 4.07 (2H, t, J=6.6 Hz), 4.12 (2H, s), 4.23 (2H, q, J=6.9 Hz), 4.65 (2H, s), 6.58-6.63 (2H, m), 7.03-7.06 (2H, m), 7.20-7.32 (5H, m), 7.55-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 649(1); Yield: 94% (white solid).
1H-NMR (DMSO-d6) δ: 0.91 (3H, t, J=7.5 Hz), 1.20 (9H, s), 1.34-1.48 (4H, m), 1.79 (2H, quint, J=6.9 Hz), 4.08-4.21 (4H, m), 4.52 (2H, s), 6.47 (2H, d, J=9.0 Hz), 7.12-7.25 (5H, m), 7.43 (2H, d, J=9.0 Hz), 7.79 (2H, d, J=9.0 Hz), 12.58 (1H, brs).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: 2-chloro-5-nitrophenol and 1-bromoheptane; Yield: 98% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.84-0.95 (3H, m), 1.33-1.56 (8H, m), 1.80-1.96 (2H, m), 4.12 (2H, t, J=6.3 Hz), 7.47-7.55 (1H, m), 7.74-7.82 (2H, m).
The title compound was obtained in the same manner as the Example 371(1) using the following starting materials.
Starting materials: the intermediate 650(1) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 80% (colorless oil).
1H-NMR (CDCl3) δ: 0.84-0.92 (3H, m), 1.20-1.44 (8H, m), 1.71-1.83 (2H, m), 4.02-4.13 (2H, m), 7.20-7.35 (2H, m), 7.44 (1H, d, J=8.4 Hz), 7.53-7.60 (2H, m), 7.81 (1H, d, J=2.1 Hz), 7.90 (1H, dd, J=2.1, 8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 650(2); Yield: 46% (purple oil).
1H-NMR (CDCl3) δ: 0.83-0.93 (3H, m), 1.20-1.43 (8H, m), 1.64-1.77 (2H, m), 3.74 (2H, brs), 3.91 (2H, t, J=6.6 Hz), 6.31 (1H, d, J=2.4 Hz), 6.35 (1H, dd, J=2.4, 8.1 Hz), 7.10 (1H, d, J=8.1 Hz), 7.15-7.22 (2H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 650(3) and 4-phenylbutyl bromide; Yield: 55% (brown oil).
1H-NMR (CDCl3) δ: 0.83-0.93 (3H, m), 1.20-1.43 (8H, m), 1.61-1.84 (6H, m), 2.68 (2H, t, J=6.9 Hz), 3.16 (2H, t, J=6.9 Hz), 3.69 (1H, brs), 3.94 (2H, t, J=6.6 Hz), 6.19 (1H, d, J=1.8 Hz), 6.25 (1H, dd, J=1.8, 8.4 Hz), 7.12 (1H, d, J=8.4 Hz), 7.14-7.34 (7H, m), 7.48-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 650(4) and methyl chloroglyoxylate; Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.93 (3H, m), 1.20-1.43 (8H, m), 1.59-1.80 (6H, m), 2.63 (2H, t, J=6.9 Hz), 3.56-3.64 (1H, m), 3.60 (3H, s), 3.80-3.88 (1H, m), 3.91 (2H, t, J=6.6 Hz), 6.75 (1H, d, J=1.8 Hz), 6.81 (1H, dd, J=1.8, 8.4 Hz), 7.10-7.31 (8H, m), 7.51-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 650(5); Yield: 93% (colorless oil).
1H-NMR (CDCl3) δ: 0.82-0.92 (3H, m), 1.17-1.38 (8H, m), 1.51-1.71 (6H, m), 2.52-2.63 (2H, m), 3.70-3.89 (4H, m), 6.65-6.78 (2H, m), 7.03-7.27 (8H, m), 7.43-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and sodium methoxide; Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 4.01 (3H, s), 7.18 (1H, d, J=9.0 Hz), 7.28-7.33 (2H, m), 7.54-7.58 (2H, m), 7.74 (1H, dd, J=2.7, 9.0 Hz), 8.05 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 651(1); Yield: 97% (white solid).
1H-NMR (CDCl3) δ: 3.89 (5H, brs), 6.83-6.96 (3H, m), 7.22-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 651(2) and 4-phenylbutyl bromide; Yield: 25% (white solid).
1H-NMR (CDCl3) δ: 1.74-1.77 (4H, m), 2.64-2.70 (2H, m), 3.18-3.23 (2H, m), 3.88 (3H, s), 4.22-4.27 (1H, m), 6.73-6.82 (3H, m), 7.19-7.28 (7H, m), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 651(3) and methyl chloroglyoxylate; Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 1.58-1.70 (4H, m), 2.57-2.63 (2H, m), 3.49-3.58 (4H, m), 3.88 (3H, s), 3.97-4.07 (1H, m), 7.00 (1H, d, J=8.7 Hz), 7.10-7.16 (3H, m), 7.20-7.32 (5H, m), 7.47-7.54 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 651(4); Yield: 88% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.35-1.52 (4H, m), 3.33 (3H, s), 3.56-3.85 (4H, m), 7.07-7.20 (6H, m), 7.40-7.44 (2H, m), 7.48-7.54 (2H, m), 7.62-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.35-1.52 (4H, m), 3.33 (3H, s), 3.56-3.85 (4H, m), 7.07-7.20 (5H, m), 7.27 (1H, d, J=2.1 Hz), 7.40-7.44 (2H, m), 7.48-7.60 (2H, m), 7.68-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-hexanol; Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.38 (4H, m), 1.49-1.56 (2H, m), 1.84-1.90 (2H, m), 4.17 (2H, t, J=6.6 Hz), 7.15-7.19 (2H, m), 7.32-7.35 (2H, m), 7.56-7.62 (2H, m), 7.94 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 652(1); Yield: 89% (white solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.38 (4H, m), 1.49-1.56 (2H, m), 1.80-1.89 (2H, m), 3.90 (2H, brs), 4.06 (2H, t, J=6.6 Hz), 6.77 (1H, d, J=7.8 Hz), 6.97-7.01 (2H, m), 7.22-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 652(2) and 4-phenylbutyl bromide; Yield: 91% (yellow solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.52 (8H, m), 1.75-1.89 (4H, m), 2.68-2.73 (2H, m), 3.17-3.24 (2H, m), 4.06 (2H, t, J=6.6 Hz), 4.26-4.32 (1H, m), 6.64 (1H, d, J=8.4 Hz), 6.95 (1H, d, J=2.7 Hz), 7.07 (1H, dd, J=2.7, 8.4 Hz), 7.18-7.31 (7H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 652(3) and methyl chloroglyoxylate; Yield: 69% (colorless oil).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.52 (6H, m), 1.75-1.89 (6H, m), 2.58-2.65 (2H, m), 3.54-3.60 (4H, m), 3.98-4.16 (3H, m), 7.07-7.18 (6H, m), 7.21-7.31 (4H, m), 7.58-7.61 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 652(4); Yield: 96% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.88 (3H, m), 1.28-1.52 (10H, m), 1.66-1.75 (2H, m), 2.48-2.52 (2H, m), 3.62-4.08 (4H, m), 7.10-7.23 (8H, m), 7.43-7.46 (2H, m), 7.79-7.82 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.88 (3H, m), 1.28-1.52 (10H, m), 1.66-1.75 (2H, m), 2.48-2.52 (2H, m), 3.12-4.08 (4H, m), 7.07-7.29 (8H, m), 7.43-7.46 (2H, m), 7.81-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 367(1) and 1-octanol; Yield: 83% (yellow solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.38 (8H, m), 1.49-1.56 (2H, m), 1.84-1.90 (2H, m), 4.17 (2H, t, J=6.6 Hz), 7.15-7.19 (2H, m), 7.32-7.35 (2H, m), 7.56-7.62 (2H, m), 7.94 (1H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 653(1); Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.56 (10H, m), 1.80-1.89 (2H, m), 3.89 (2H, brs), 4.05 (2H, t, J=6.6 Hz), 6.77 (1H, d, J=7.8 Hz), 6.97-7.01 (2H, m), 7.22-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 653(2) and 4-phenylbutyl bromide; Yield: 57% (white solid).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.52 (12H, m), 1.75-1.89 (4H, m), 2.68-2.73 (2H, m), 3.17-3.24 (2H, m), 4.06 (2H, t, J=6.6 Hz), 4.26-4.32 (1H, m), 6.64 (1H, d, J=8.4 Hz), 6.95 (1H, d, J=2.7 Hz), 7.07 (1H, dd, J=2.7, 8.4 Hz), 7.18-7.31 (7H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 653(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.89-0.94 (3H, m), 1.32-1.52 (10H, m), 1.75-1.89 (6H, m), 2.58-2.65 (2H, m), 3.54-3.60 (4H, m), 3.98-4.16 (3H, m), 7.06-7.18 (6H, m), 7.21-7.31 (4H, m), 7.57-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 653(4); Yield: 64% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.88 (3H, m), 1.23-1.52 (14H, m), 1.66-1.75 (2H, m), 2.48-2.52 (2H, m), 3.62-4.08 (4H, m), 7.10-7.23 (8H, m), 7.43-7.46 (2H, m), 7.79-7.82 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.88 (3H, m), 1.23-1.52 (14H, m), 1.66-1.75 (2H, m), 2.48-2.52 (2H, m), 3.12-4.08 (4H, m), 7.07-7.29 (8H, m), 7.43-7.46 (2H, m), 7.81-7.84 (2H, m).
The title compound was obtained in the same manner as the Example 371(1) using the following starting materials.
Starting materials: 2-chloro-5-nitrophenol and 4-(trifluoromethoxy)phenylboronic acid; Yield: 7% (yellow solid).
1H-NMR (CDCl3) δ: 5.58 (1H, s), 7.36-7.42 (3H, m), 7.53-7.57 (2H, m), 7.84-7.90 (2H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 654(1) and 1-chloropentane; Yield: 75% (yellow solid).
1H-NMR (CDCl3) δ: 0.87-0.92 (3H, m), 1.32-1.38 (4H, m), 1.75-1.81 (2H, m), 4.08 (2H, t, J=6.6 Hz), 7.27-7.30 (2H, m), 7.44 (1H, d, J=8.7 Hz), 7.57-7.60 (2H, m), 7.81 (1H, d, J=2.1 Hz), 7.90 (1H, dd, J=2.1, 8.7 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 654(2); Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.32-1.38 (4H, m), 1.69-1.74 (2H, m), 3.73 (2H, brs), 3.90 (2H, t, J=6.6 Hz), 6.30-6.36 (2H, m), 7.10 (1H, d, J=7.8 Hz), 7.17-7.21 (2H, m), 7.50-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 654(3) and methyl chloroglyoxylate; Yield: 67% (white solid).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.30-1.38 (4H, m), 1.69-1.78 (2H, m), 3.98-4.02 (5H, m), 7.11 (1H, dd, J=2.1, 8.4 Hz), 7.21-7.25 (2H, m), 7.30 (1H, d, J=8.4 Hz), 7.53-7.56 (3H, m), 8.89 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 654(4) and 4-phenylbutyl bromide; Yield: 85% (yellow oil).
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.30-1.38 (4H, m), 1.65-1.75 (6H, m), 2.61-2.65 (2H, m), 3.61 (3H, s), 3.81-3.92 (4H, m), 6.76 (1H, d, J=2.1 Hz), 6.82 (1H, dd, J=2.1, 8.4 Hz), 7.13-7.29 (8H, m), 7.53-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 654(5); Yield: 82% (white solid).
1H-NMR (DMSO-d6) δ: 0.83 (3H, t, J=6.9 Hz), 1.21-1.31 (4H, m), 1.40-1.51 (4H, m), 1.62-1.66 (2H, m), 2.50-2.54 (2H, m), 3.71 (2H, t, J=6.6 Hz), 3.92 (2H, t, J=6.0 Hz), 6.90-6.94 (1H, m), 7.08-7.15 (4H, m), 7.20-7.25 (3H, m), 7.38-7.41 (2H, m), 7.60-7.63 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 194(2) and benzyl 3-bromopropyl ether; Yield: 60% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.34-1.50 (4H, m), 1.80 (2H, quint, J=7.2 Hz), 2.00 (2H, quint, J=6.0 Hz), 3.35 (2H, t, J=6.6 Hz), 3.63 (2H, t, J=5.7 Hz), 4.00 (2H, t, J=6.9 Hz), 4.53 (2H, s), 6.79-6.82 (3H, m), 7.20-7.36 (7H, m), 7.52-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 655(1) and methyl chloroglyoxylate; Yield: 99% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.86-0.95 (3H, m), 1.23-1.48 (4H, m), 1.77-1.95 (4H, m), 3.53-3.57 (5H, m), 3.97-4.14 (4H, m), 4.44 (2H, s), 6.98 (1H, d, J=8.4 Hz), 7.23-7.30 (7H, m), 7.37 (1H, d, J=2.4 Hz), 7.45-7.50 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 655(2); Yield: 61% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.91 (3H, m), 1.24-1.46 (4H, m), 1.60-1.79 (4H, m), 3.34-4.09 (6H, m), 4.32-4.34 (2H, m), 7.09 (1H, d, J=8.4 Hz), 7.20-7.72 (11H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.85-0.91 (3H, m), 1.24-1.46 (4H, m), 1.60-1.79 (4H, m), 3.34-4.09 (6H, m), 4.32-4.34 (2H, m), 7.16 (1H, d, J=8.7 Hz), 7.20-7.72 (11H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and 3-cyclohexyl-1-propanol; Yield: 79% (orange solid).
1H-NMR (CDCl3) δ: 0.88-0.99 (2H, m), 1.16-1.40 (6H, m), 1.63-1.92 (7H, m), 4.13 (2H, t, J=6.6 Hz), 7.15 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m), 7.55-7.58 (2H, m), 7.70 (1H, dd, J=2.4, 8.7 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 656(1); Yield: 88% (white solid).
1H-NMR (CDCl3) δ: 0.88-0.99 (2H, m), 1.16-1.40 (6H, m), 1.63-1.92 (7H, m), 3.88 (2H, brs), 4.01 (2H, t, J=6.6 Hz), 6.83 (1H, d, J=7.8 Hz), 6.88-6.93 (2H, m), 7.22-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 656(2) and 4-phenylbutyl bromide; Yield: 51% (white solid).
1H-NMR (CDCl3) δ: 0.88-0.99 (2H, m), 1.16-1.40 (6H, m), 1.63-1.92 (11H, m), 2.69 (2H, t, J=7.2 Hz), 3.20-3.24 (2H, m), 4.00 (2H, t, J=6.6 Hz), 4.26-4.28 (1H, m), 6.73-6.80 (3H, m), 7.19-7.31 (7H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 656(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.88-0.99 (2H, m), 1.16-1.36 (6H, m), 1.63-1.85 (11H, m), 2.57-2.63 (2H, m), 3.54-3.61 (4H, m), 3.94-4.05 (3H, m), 6.98 (1H, d, J=8.4 Hz), 7.10-7.16 (3H, m), 7.20-7.32 (5H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 656(4); Yield: 99% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ 0.83-0.93 (2H, m), 1.15-1.73 (17H, m), 2.57-2.63 (2H, m), 3.58-3.63 (1H, m), 3.96-4.05 (3H, m), 7.06-7.20 (6H, m), 7.40-7.44 (2H, m), 7.48-7.57 (2H, m), 7.63-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.83-0.93 (2H, m), 1.15-1.73 (17H, m), 2.57-2.63 (2H, m), 3.10-3.28 (1H, m), 3.96-4.05 (3H, m), 7.06-7.20 (5H, m), 7.26-7.29 (1H, m), 7.40-7.44 (2H, m), 7.48-7.57 (2H, m), 7.67-7.70 (2H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 354(1) and 3-phenoxypropyl bromide; Yield: 80% (yellow oil).
1H-NMR (CDCl3) δ: 2.26-2.41 (2H, m), 4.22 (2H, t, J=6.0 Hz), 4.36 (2H, t, J=6.0 Hz), 6.88-7.00 (3H, m), 7.19 (1H, d, J=8.7 Hz), 7.24-7.36 (4H, m), 7.50-7.60 (2H, m), 7.70 (1H, dd, J=2.4, 8.4 Hz), 8.04 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 657(1); Yield: 57% (yellow solid).
1H-NMR (CDCl3) δ: 2.24-2.40 (2H, m), 3.88 (2H, s), 4.18 (2H, t, J=6.0 Hz), 4.25 (2H, t, J=6.0 Hz), 6.83-7.00 (6H, m), 7.18-7.34 (4H, m), 7.47-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 657(2) and iodopentane; Yield: 23% (white solid).
1H-NMR (CDCl3) δ: 0.83-1.00 (3H, m), 1.28-1.48 (4H, m), 1.58-1.74 (2H, m), 2.24-2.40 (2H, m), 3.16 (2H, t, J=6.9 Hz), 4.17 (2H, t, J=6.3 Hz), 4.20-4.32 (3H, m), 6.72-6.87 (3H, m), 6.87-7.01 (3H, m), 7.19-7.35 (4H, m), 7.50-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 657(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.75-0.94 (3H, m), 1.11-1.40 (4H, m), 1.42-1.64 (2H, m), 2.22-2.39 (2H, m), 3.38-3.56 (4H, m), 3.85-4.00 (1H, m), 4.08-4.34 (4H, m), 6.88-6.98 (3H, m), 7.05 (1H, d, J=8.4 Hz), 7.22-7.34 (4H, m), 7.37 (1H, d, J=2.4 Hz), 7.47-7.58 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 657(4); Yield: 80% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.59-0.83 (3H, m), 0.83-1.20 (4H, m), 1.20-1.56 (2H, m), 1.80-2.16 (2H, m), 3.15-4.18 (6H, m), 6.60-6.99 (4H, m), 7.00-7.30 (6H, m), 7.30-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and cyclopentanol; Yield: 70% (orange solid).
1H-NMR (CDCl3) δ: 1.64-1.97 (8H, m), 4.93-4.98 (1H, m), 7.15 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m), 7.55-7.58 (2H, m), 7.68 (1H, dd, J=2.4, 8.7 Hz), 8.00 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 658(1); Yield: 87% (white solid).
1H-NMR (CDCl3) δ: 1.64-1.97 (8H, m), 3.88 (2H, brs), 4.80-4.86 (1H, m), 6.83 (1H, d, J=7.8 Hz), 6.87-6.92 (2H, m), 7.22-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 658(2) and 4-phenylbutyl bromide; Yield: 89% (yellow oil).
1H-NMR (CDCl3) δ: 1.64-1.97 (12H, m), 2.69 (2H, t, J=7.2 Hz), 3.20-3.24 (2H, m), 4.23 (1H, brs), 4.80-4.86 (1H, m), 6.73-6.80 (3H, m), 7.19-7.31 (7H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 658(3) and methyl chloroglyoxylate; Yield: 75% (colorless oil).
1H-NMR (CDCl3) δ: 1.57-1.91 (12H, m), 2.57-2.62 (2H, m), 3.50-3.59 (4H, m), 3.89-4.02 (1H, m), 4.79-4.86 (1H, m), 6.97 (1H, d, J=8.7 Hz), 7.10-7.16 (3H, m), 7.20-7.32 (5H, m), 7.47-7.51 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 658(4); Yield: 90% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.33-1.88 (12H, m), 2.57-2.62 (2H, m), 3.10-4.11 (2H, m), 4.86-4.93 (1H, m), 7.04-7.17 (6H, m), 7.40-7.43 (2H, m), 7.48-7.55 (2H, m), 7.63-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.33-1.88 (12H, m), 2.57-2.62 (2H, m), 3.10-4.11 (2H, m), 4.86-4.93 (1H, m), 7.04-7.17 (5H, m), 7.27-7.29 (1H, m), 7.40-7.43 (2H, m), 7.48-7.55 (2H, m), 7.67-7.70 (2H, m).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: the intermediate 188(1) and cycloheptanol; Yield: 72% (white solid).
1H-NMR (CDCl3) δ: 1.48-2.09 (12H, m), 4.60-4.69 (1H, m), 7.11 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m), 7.54-7.58 (2H, m), 7.67 (1H, dd, J=2.4, 8.7 Hz), 7.98 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 659(1); Yield: 81% (white solid).
1H-NMR (CDCl3) δ: 1.48-1.90 (10H, m), 2.03-2.08 (2H, m), 3.88 (2H, brs), 4.44-4.48 (1H, m), 6.81 (1H, d, J=8.1 Hz), 6.87-6.93 (2H, m), 7.22-7.25 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 659(2) and 4-phenylbutyl bromide; Yield: 72% (yellow oil).
1H-NMR (CDCl3) δ: 1.48-1.90 (14H, m), 2.03-2.08 (2H, m), 2.69 (2H, t, J=7.2 Hz), 3.15-3.21 (2H, m), 4.30 (1H, brs), 4.41-4.49 (1H, m), 6.73-6.80 (3H, m), 7.19-7.31 (7H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 659(3) and methyl chloroglyoxylate; Yield: 80% (colorless oil).
1H-NMR (CDCl3) δ: 1.48-1.85 (14H, m), 1.95-2.05 (2H, m), 2.57-2.62 (2H, m), 3.50-3.59 (4H, m), 3.98-4.05 (1H, m), 4.48-4.51 (1H, m), 6.92 (1H, d, J=8.4 Hz), 7.10-7.16 (3H, m), 7.20-7.22 (2H, m), 7.24-7.28 (2H, m), 7.32 (1H, d, J=2.4 Hz), 7.45-7.50 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 659(4); Yield: 67% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.33-1.73 (14H, m), 1.89-2.01 (2H, m), 2.57-2.62 (2H, m), 3.21-3.97 (2H, m), 4.52-4.63 (1H, m), 7.03-7.20 (6H, m), 7.40-7.43 (2H, m), 7.48-7.55 (2H, m), 7.63-7.67 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.33-1.73 (14H, m), 1.89-2.01 (2H, m), 2.57-2.62 (2H, m), 3.21-3.97 (2H, m), 4.52-4.63 (1H, m), 7.03-7.20 (5H, m), 7.28-7.29 (1H, m), 7.40-7.43 (2H, m), 7.48-7.55 (2H, m), 7.67-7.69 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and methyl 4-(bromomethyl)benzoate; Yield: 63% (white solid).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 3.91 (3H, s), 5.03 (2H, s), 7.09-7.17 (2H, m), 7.24-7.37 (4H, m), 7.47-7.59 (4H, m), 7.93-8.02 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 660(1); Yield: 67% (pale yellow solid).
1H-NMR (CDCl3) δ: 5.04 (2H, s), 7.00-7.62 (10H, m), 7.93-8.02 (2H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 125(3) and 2-(bromomethyl)naphthalene; Yield: 86% (colorless oil).
1H-NMR (CDCl3) δ: 3.60 (3H, s), 5.15 (2H, s), 7.11-7.17 (2H, m), 7.22-7.30 (2H, m), 7.40-7.57 (7H, m), 7.54-7.88 (3H, m), 7.66 (1H, s).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 661(1); Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 5.13 (2H, s), 7.07-7.14 (2H, m), 7.22-7.30 (2H, m), 7.35-7.57 (7H, m), 7.63 (1H, brs), 7.70-7.89 (3H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 354(1) and 3,5-dimethylbenzyl bromide; Yield: 96% (yellow solid).
1H-NMR (CDCl3) δ: 2.34 (6H, s), 5.22 (2H, s), 6.98 (1H, s), 7.08 (2H, s), 7.19 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m), 7.54-7.58 (2H, m), 7.68 (1H, dd, J=2.4, 8.7 Hz), 8.06 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 662(1); Yield: 63% (white solid).
1H-NMR (CDCl3) δ: 2.32 (6H, s), 3.94 (2H, brs), 5.05 (2H, s), 6.90-6.94 (3H, m), 6.99 (1H, s), 7.07 (2H, s), 7.21-7.25 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 662(2) and 4-phenylbutyl bromide; Yield: 25% (white solid).
1H-NMR (CDCl3) δ: 1.46-1.58 (2H, m), 1.70-1.79 (2H, m), 2.33 (6H, s), 2.65-2.69 (2H, m), 3.18-3.23 (2H, m), 4.31-4.35 (1H, m), 5.03 (2H, s), 6.75-6.81 (2H, m), 6.88 (1H, d, J=8.4 Hz), 6.99 (1H, s), 7.05 (2H, s), 7.16-7.29 (7H, m), 7.52-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 662(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.56-1.68 (4H, m), 2.33 (6H, s), 2.50-2.61 (2H, m), 3.50-3.59 (4H, m), 4.01-4.11 (1H, m), 5.09 (2H, s), 6.97 (1H, s), 7.02-7.15 (4H, m), 7.18-7.23 (2H, m), 7.26-7.29 (2H, m), 7.32 (1H, d, J=2.4 Hz), 7.45-7.50 (5H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 662(4); Yield: 98% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.37-1.48 (4H, m), 2.26 (6H, s), 2.48-2.52 (2H, m), 3.20-4.04 (2H, m), 5.11 (2H, s), 6.94 (1H, s), 7.03-7.19 (8H, m), 7.41-7.44 (2H, m), 7.47-7.51 (2H, m), 7.63-7.66 (2H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.37-1.48 (4H, m), 2.26 (6H, s), 2.48-2.52 (2H, m), 3.20-4.04 (2H, m), 5.11 (2H, s), 6.91 (1H, s), 7.03-7.19 (7H, m), 7.32 (1H, d, J=2.7 Hz), 7.41-7.44 (2H, m), 7.47-7.57 (2H, m), 7.68-7.71 (2H, m).
The title compound was obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and cyclopentanone; Yield: 33% (white solid).
1H-NMR (CDCl3) δ: 1.47-1.80 (6H, m), 2.00-2.10 (2H, m), 3.79 (1H, brs), 3.83 (1H, quint, J=6.0 Hz), 6.64-6.69 (2H, m), 7.21-7.25 (2H, m), 7.36-7.41 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 663(1) and methyl chloroglyoxylate; Yield: 79% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.43-1.62 (6H, m), 1.95-2.05 (2H, m), 3.51 (3H, s), 4.80-4.92 (1H, m), 7.27-7.33 (4H, m), 7.56-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 663(2); Yield: 86% (white solid).
1H-NMR (DMSO-d6) δ: 1.34-1.62 (6H, m), 1.83-2.01 (2H, m), 4.70 (1H, quint, J=8.4 Hz), 7.38 (2H, d, J=8.4 Hz), 7.48 (2H, d, J=8.1 Hz), 7.77 (2H, d, J=8.4 Hz), 7.84 (2H, d, J=9.0 Hz), 13.77 (1H, brs).
The title compound was obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and cycloheptanone; Yield: 28% (pale brown solid).
1H-NMR (CDCl3) δ: 1.45-1.80 (10H, m), 1.99-2.07 (2H, m), 3.37-3.54 (1H, m), 3.76 (1H, brs), 6.58-6.65 (2H, m), 7.18-7.23 (2H, m), 7.36-7.40 (2H, m), 7.46-7.53 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 664(1) and methyl chloroglyoxylate; Yield: 77% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.36-1.70 (10H, m), 1.99-2.05 (2H, m), 3.50 (3H, s), 4.50-4.63 (1H, m), 7.27-7.32 (4H, m), 7.54-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 664(2); Yield: 77% (white solid).
1H-NMR (DMSO-d6) δ: 1.38-1.63 (10H, m), 1.88-2.02 (2H, m), 4.35-4.50 (1H, m), 7.38 (2H, d, J=8.4 Hz), 7.48 (2H, d, J=7.8 Hz), 7.76 (2H, d, J=8.4 Hz), 7.84 (2H, d, J=9.0 Hz), 13.74 (1H, brs).
The title compound and the geometric isomer (the intermediate 666(1)) were obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 4-(tert-butyl)cyclohexanone; Yield: 39% (white solid).
1H-NMR (CDCl3) δ: 0.87 (9H, s), 1.05-1.27 (4H, m), 1.51-1.64 (3H, m), 1.97-2.02 (2H, m), 3.66-3.74 (1H, m), 3.95 (1H, brs), 6.66-6.70 (2H, m), 7.20-7.25 (2H, m), 7.37-7.41 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 665(1) and methyl chloroglyoxylate; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 0.81 (9H, s), 1.14-1.39 (5H, m), 1.75-1.91 (2H, m), 1.92-2.20 (2H, m), 3.50 (3H, s), 4.41-4.49 (1H, m), 7.25-7.32 (4H, m), 7.53-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 665(2); Yield: 98% (white solid).
1H-NMR (DMSO-d6) δ: 0.64 (9H, s), 0.73-0.98 (3H, m), 1.25-1.36 (2H, m), 1.58-1.69 (2H, m), 2.01-2.05 (2H, m), 4.40-4.60 (1H, m), 7.46-7.49 (4H, m), 7.76 (2H, d, J=8.1 Hz), 7.82 (2H, d, J=9.0 Hz), 13.66 (1H, brs).
The title compound and the geometric isomer (the intermediate 665(1)) were obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 4-(tert-butyl)cyclohexanone; Yield: 20% (white solid).
1H-NMR (CDCl3) δ: 0.88 (9H, s), 1.04-1.23 (5H, m), 1.83-1.86 (2H, m), 2.18-2.22 (2H, m), 3.16-3.28 (1H, m), 3.61 (1H, brs), 6.62-6.67 (2H, m), 7.20-7.23 (2H, m), 7.35-7.40 (2H, m), 7.47-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 666(1) and methyl chloroglyoxylate; Yield: 98% (white solid).
1H-NMR (CDCl3) δ: 0.69 (9H, s), 0.81-1.09 (3H, m), 1.41-1.47 (2H, m), 1.66-1.77 (2H, m), 2.05-2.12 (2H, m), 3.49 (3H, s), 4.60-4.72 (1H, m), 7.31 (2H, d, J=8.1 Hz), 7.39 (2H, d, J=8.4 Hz), 7.55-7.62 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 666(2); Yield: 90% (white solid).
1H-NMR (DMSO-d6) δ: 0.78 (9H, s), 1.08-1.24 (5H, m), 1.68-1.99 (4H, m), 3.98-4.23 (1H, m), 7.35 (2H, d, J=8.4 Hz), 7.48 (2H, d, J=8.1 Hz), 7.75 (2H, d, J=8.4 Hz), 7.78-7.85 (2H, m), 13.72 (1H, brs).
The title compound and the geometric isomer (the intermediate 668(1)) were obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 4-methylcyclohexanone; Yield: 24% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, d, J=6.3 Hz), 1.18-1.30 (2H, m), 1.55-1.83 (7H, m), 3.57-3.62 (1H, m), 3.89 (1H, brs), 6.64-6.68 (2H, m), 7.20-7.23 (2H, m), 7.36-7.40 (2H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 667(1) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.80 (3H, d, J=7.2 Hz), 1.45-1.56 (4H, m), 1.58-1.74 (4H, m), 1.84-1.99 (1H, m), 3.50 (3H, s), 4.41-4.52 (1H, m), 7.25-7.33 (4H, m), 7.55-7.65 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 667(2); Yield: 89% (white solid).
1H-NMR (DMSO-d6) δ: 0.75 (3H, d, J=6.9 Hz), 1.34-1.83 (9H, m), 4.15-4.35 (1H, m), 7.38 (2H, d, J=8.1 Hz), 7.47 (2H, d, J=8.7 Hz), 7.77 (2H, d, J=8.1 Hz), 7.85 (2H, d, J=8.7 Hz), 13.70 (1H, brs).
The title compound and the geometric isomer (the intermediate 667(1)) were obtained in the same manner as the Example 253(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 4-methylcyclohexanone; Yield: 45% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, d, J=6.6 Hz), 1.00-1.21 (4H, m), 1.30-1.46 (1H, m), 1.75-1.78 (2H, m), 2.11-2.15 (2H, m), 3.17-3.25 (1H, m), 3.60 (1H, brs), 6.61-6.66 (2H, m), 7.20-7.25 (2H, m), 7.36-7.39 (2H, m), 7.49-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 668(1) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.86 (3H, d, J=6.0 Hz), 1.07-1.33 (5H, m), 1.72-1.76 (2H, m), 1.90-1.94 (2H, m), 3.50 (3H, s), 4.41-4.60 (1H, m), 7.24-7.32 (4H, m), 7.54-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 668(2); Yield: 89% (white solid).
1H-NMR (DMSO-d6) δ: 0.83 (3H, d, J=6.0 Hz), 1.05-1.28 (5H, m), 1.68-1.85 (4H, m), 4.19-4.40 (1H, m), 7.35 (2H, d, J=8.4 Hz), 7.48 (2H, d, J=8.4 Hz), 7.75 (2H, d, J=8.4 Hz), 7.82-7.85 (2H, m), 13.67 (1H, brs).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 1-iododecane; Yield: 86% (white solid).
1H-NMR (CDCl3) δ: 0.84-0.95 (3H, m), 1.23-1.49 (14H, m), 1.52-1.70 (2H, m), 3.14 (2H, t, J=7.2 Hz), 3.74 (1H, brs), 6.62-6.71 (2H, m), 7.18-7.28 (2H, m), 7.35-7.43 (2H, m), 7.48-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 669(1) and methyl chloroglyoxylate; Yield: 71% (colorless oil).
1H-NMR (CDCl3) δ: 0.83-0.93 (3H, m), 1.14-1.42 (14H, m), 1.50-1.65 (2H, m), 3.58 (3H, s), 3.75-3.85 (2H, m), 6.62-6.71 (2H, m), 7.18-7.28 (2H, m), 7.35-7.43 (2H, m), 7.48-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 669(2); Yield: 86% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.82-0.92 (3H, m), 1.17-1.37 (14H, m), 1.50-1.65 (2H, m), 3.72-3.82 (2H, m), 7.20-7.33 (4H, m), 7.53-7.62 (4H, m).
A solution of 4-(2,5-dimethylphenyl)butyric acid (271 mg, 1.410 mmol) in anhydrous tetrahydrofuran (1 ml) was added dropwise to a suspension of lithium aluminium hydride (58 mg, 1.410 mmol) in anhydrous tetrahydrofuran (2 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was cooled to 0° C., diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (150 mg, 60%) as a colorless oil.
1H-NMR (CDCl3) δ: 1.58-1.67 (4H, m), 2.26 (3H, s), 2.29 (3H, s), 2.54-2.62 (2H, m), 3.63-3.71 (2H, m), 6.88-6.95 (2H, m), 6.99-7.04 (1H, m).
A mixture of the intermediate 670(1) (150 mg, 0.841 mmol), triphenylphosphine (331 mg, 1.262 mmol), tetrabromomethane (474 mg, 1.430 mmol) and dichloromethane (3 ml) was stirred at room temperature for 2 hours. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=1:1) to give the title compound (174 mg, 86%) as a clear colorless oil.
1H-NMR (CDCl3) δ: 1.68-1.77 (2H, m), 1.89-1.97 (2H, m), 2.26 (3H, s), 2.29 (3H, s), 2.56-2.61 (2H, m), 3.44 (2H, t, J=6.9 Hz), 6.90-6.95 (2H, m), 7.01-7.05 (1H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediates 670 (2) and 194 (2); Yield: 61% (white solid).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.38-1.51 (4H, m), 1.68-1.88 (6H, m), 2.26 (3H, s), 2.28 (3H, s), 2.60-2.65 (2H, m), 3.20-3.26 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.29 (1H, brs), 6.74-6.81 (3H, m), 6.88-6.98 (2H, m), 7.01-7.05 (1H, m), 7.22-7.26 (2H, m), 7.52-7.57 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 670(3) and methyl chloroglyoxylate; Yield: 82% (colorless oil).
1H-NMR (CDCl3) δ: 0.86-0.95 (3H, m), 1.23-1.85 (10H, m), 2.20 (3H, s), 2.23 (3H, s), 2.51-2.57 (2H, m), 3.50-3.60 (1H, m), 3.53 (3H, s), 3.95-4.08 (3H, m), 6.85-7.01 (4H, m), 7.26-7.29 (2H, m), 7.34 (1H, d, J=2.1 Hz), 7.48-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 670(4); Yield: 70% (colorless oil).
1H-NMR (DMSO-d6) δ: 0.83-0.92 (3H, m), 1.24-1.73 (10H, m), 2.10-2.16 (6H, m), 2.38-2.50 (2H, m), 3.15-4.03 (4H, m), 6.65-6.94 (3H, m), 7.06-7.18 (1H, m), 7.30-7.72 (6H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: 1-bromo-4-nitrobenzene and 2-naphthaleneboronic acid; Yield: 99% (white solid).
1H-NMR (CDCl3) δ: 7.53-7.59 (2H, m), 7.75 (1H, dd, J=1.8, 8.4 Hz), 7.84-8.03 (5H, m), 8.10 (1H, d, J=1.8 Hz), 8.31-8.39 (2H, m).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 671(1); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 3.71 (2H, brs), 6.77-6.82 (2H, m), 7.40-7.60 (4H, m), 7.70 (1H, dd, J=1.8, 8.4 Hz), 7.80-7.90 (3H, m), 7.97 (1H, d, J=1.8 Hz).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 671(2) and 4-phenylbutyl bromide; Yield: 15% (brown oil).
1H-NMR (CDCl3) δ: 1.63-1.83 (4H, m), 2.68 (2H, t, J=7.5 Hz), 3.20 (2H, t, J=7.5 Hz), 3.72 (1H, brs), 6.67-6.74 (2H, m), 7.15-7.34 (5H, m), 7.37-7.50 (2H, m), 7.53-7.61 (2H, m), 7.71 (1H, dd, J=1.8, 8.4 Hz), 7.79-7.88 (3H, m), 7.94-7.98 (1H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 671(3) and methyl chloroglyoxylate; Yield: 60% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.58-1.74 (4H, m), 2.63 (2H, t, J=7.5 Hz), 3.59 (3H, s), 3.86 (2H, t, J=7.5 Hz), 7.11-7.33 (7H, m), 7.47-7.57 (2H, m), 7.67-7.76 (3H, m), 7.85-7.97 (3H, m), 8.02-8.05 (1H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 671(4); Yield: 78% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.60-1.74 (4H, m), 2.57-2.67 (2H, m), 3.79-3.88 (2H, m), 7.10-7.31 (7H, m), 7.47-7.57 (2H, m), 7.67-7.76 (3H, m), 7.85-7.97 (3H, m), 8.02-8.05 (1H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 359(4) and 3,5-dimethyphenylboronic acid; Yield: 80% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=6.9 Hz), 1.30-1.49 (4H, m), 1.57-1.69 (4H, m), 1.71-1.86 (2H, m), 2.37 (6H, s), 2.55-2.65 (2H, m), 3.53 (3H, s), 3.86-4.05 (3H, m), 4.70-4.79 (1H, m), 6.44-6.48 (2H, m), 6.54-6.59 (1H, m), 6.92-7.00 (2H, m), 7.08-7.17 (3H, m), 7.17-7.29 (1H, m), 7.35 (1H, d, J=2.4 Hz), 7.51 (1H, dd, J=2.4, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 672(1); Yield: 11% (pale yellow oil).
1H-NMR (CDCl3) δ: 0.84-0.94 (3H, m), 1.12-1.45 (4H, m), 1.50-1.78 (6H, m), 2.35 (6H, s), 2.48-2.63 (2H, m), 3.76 (2H, brs), 3.85-4.00 (2H, m), 6.88-7.00 (2H, m), 7.04-7.38 (7H, m), 7.43-7.52 (2H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and pyrrolidine; Yield: 94% (yellow solid).
1H-NMR (CDCl3) δ: 1.81-1.90 (4H, m), 3.00-3.09 (4H, m), 6.75 (1H, d, J=9.0 Hz), 7.21-7.30 (2H, m), 7.35-7.42 (2H, m), 8.02 (1H, d, J=2.7 Hz), 8.11 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 673(1); Yield: 100% (pale green oil).
1H-NMR (CDCl3) δ: 1.67-1.77 (4H, m), 2.73-2.83 (4H, m), 3.42 (2H, brs), 6.59 (1H, d, J=2.4 Hz), 6.65 (1H, dd, J=2.4, 8.4 Hz), 6.82 (1H, d, J=8.4 Hz), 7.14-7.23 (2H, m), 7.47-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 673(2) and 4-phenylbutyl bromide; Yield: 45% (pale brown oil).
1H-NMR (CDCl3) δ: 1.55-1.79 (8H, m), 2.61-2.71 (4H, m), 2.75 (2H, brs), 3.10 (2H, brs), 3.23 (1H, brs), 6.50 (2H, brs), 6.86 (1H, brs), 7.12-7.24 (6H, m), 7.25-7.31 (1H, m), 7.48-7.57 (2H, brs).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 673(3) and methyl chloroglyoxylate; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 1.57-1.68 (4H, m), 1.74-1.83 (4H, m), 2.56-2.65 (2H, m), 2.86-2.95 (4H, m), 3.57 (3H, s), 3.70-3.79 (2H, m), 6.77 (1H, d, J=8.4 Hz), 6.92 (1H, d, J=2.4 Hz), 7.02 (1H, dd, J=2.4, 8.4 Hz), 7.08-7.26 (7H, m), 7.32-7.39 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 673(4); Yield: 92% (white solid).
1H-NMR (CDCl3) δ: 1.55-1.69 (4H, m), 1.72-1.84 (4H, m), 2.53-2.65 (2H, m), 2.84-2.96 (4H, m), 3.69-3.88 (2H, m), 6.79 (1H, d, J=9.0 Hz), 6.89 (1H, d, J=2.4 Hz), 7.00 (1H, dd, J=2.4, 9.0 Hz), 7.07-7.25 (7H, m), 7.33-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and hexamethyleneimine; Yield: 94% (yellow oil).
1H-NMR (CDCl3) δ: 1.49-1.66 (8H, m), 3.14-3.24 (4H, m), 6.98 (1H, d, J=9.0 Hz), 7.22-7.30 (2H, m), 7.38-7.46 (2H, m), 7.99 (1H, d, J=2.7 Hz), 8.09 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 674(1); Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 1.32-1.54 (8H, m), 2.84-2.94 (4H, m), 3.44 (2H, brs), 6.58 (1H, d, J=2.4 Hz), 6.63 (1H, dd, J=2.4, 8.4 Hz), 6.99 (1H, d, J=8.4 Hz), 7.17-7.25 (2H, m), 7.48-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 674(2) and 4-phenylbutyl bromide; Yield: 80% (brown oil).
1H-NMR (CDCl3) δ: 1.34-1.94 (12H, m), 2.58-3.29 (9H, m), 6.42-6.59 (2H, m), 7.00-7.33 (8H, m), 7.46-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 674(3) and methyl chloroglyoxylate; Yield: 78% (colorless oil).
1H-NMR (CDCl3) δ: 1.40-1.72 (12H, m), 2.56-2.67 (2H, m), 2.96-3.06 (4H, m), 3.56 (3H, s), 3.71-3.78 (2H, m), 6.93-6.97 (1H, m), 7.00-7.04 (2H, m), 7.07-7.27 (7H, m), 7.40-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 674(4); Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 1.40-1.72 (12H, m), 2.54-2.66 (2H, m), 2.96-3.07 (4H, m), 3.68-3.78 (2H, m), 6.91-6.96 (1H, m), 6.98-7.06 (2H, m), 7.07-7.27 (7H, m), 7.39-7.50 (2H, m).
The title compound was obtained in the same manner as the Example 208(1) using the following starting materials.
Starting materials: the intermediate 211(1) and thiomorpholine; Yield: 100% (yellow solid).
1H-NMR (CDCl3) δ: 2.50-2.57 (4H, m), 3.18-3.27 (4H, m), 7.07 (1H, d, J=9.0 Hz), 7.30-7.37 (2H, m), 7.57-7.65 (2H, m), 8.08 (1H, d, J=2.7 Hz), 8.17 (1H, dd, J=2.7, 9.0 Hz).
The title compound was obtained in the same manner as the Example 376(2) using the following starting material.
Starting material: the intermediate 675(1); Yield: 66% (white solid).
1H-NMR (CDCl3) δ: 2.42-2.54 (4H, m), 2.93-3.03 (4H, m), 3.57 (2H, brs), 6.58-6.69 (2H, m), 6.90-6.95 (1H, m), 7.17-7.27 (2H, m), 7.48-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 675(2) and 4-phenylbutyl bromide; Yield: 46% (brown oil).
1H-NMR (CDCl3) δ: 1.59-1.80 (4H, m), 2.44-2.53 (4H, m), 2.66 (2H, t, J=6.9 Hz), 2.93-3.02 (4H, m), 3.07-3.17 (2H, m), 3.51 (1H, brs), 6.47-6.59 (2H, m), 6.94 (1H, d, J=8.4 Hz), 7.14-7.32 (7H, m), 7.53-7.59 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 675(3) and methyl chloroglyoxylate; Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 1.56-1.72 (4H, m), 2.48-2.55 (4H, m), 2.61 (2H, t, J=6.9 Hz), 3.05-3.12 (4H, m), 3.57 (3H, s), 3.77 (2H, t, J=6.9 Hz), 6.96-7.20 (6H, m), 7.20-7.32 (4H, m), 7.52-7.58 (2H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 675(4); Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 1.56-1.74 (4H, m), 2.47-2.55 (4H, m), 2.56-2.66 (2H, m), 3.04-3.13 (4H, m), 3.72-3.81 (2H, m), 6.96-7.20 (6H, m), 7.20-7.31 (4H, m), 7.52-7.60 (2H, m).
The title compound was obtained in the same manner as the Example 354(2) using the following starting materials.
Starting materials: the intermediate 354(1) and 5-bromopentyl acetate; Yield: 93% (white solid).
1H-NMR (CDCl3) δ: 1.57-1.64 (2H, m), 1.70-1.77 (2H, m), 1.88-1.93 (2H, m), 2.07 (3H, s), 4.09-4.18 (4H, m), 7.15 (1H, d, J=9.0 Hz), 7.29-7.32 (2H, m), 7.54-7.58 (2H, m), 7.70 (1H, dd, J=2.4, 9.0 Hz), 8.03 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 676(1); Yield: 66% (white solid).
1H-NMR (CDCl3) δ: 1.54-1.61 (2H, m), 1.70-1.77 (2H, m), 1.83-1.93 (2H, m), 2.06 (3H, s), 3.89 (2H, brs), 4.03-4.13 (4H, m), 6.83 (1H, d, J=8.1 Hz), 6.88-6.93 (2H, m), 7.22-7.27 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 676(2) and 4-phenylbutyl bromide; Yield: 50% (colorless oil).
1H-NMR (CDCl3) δ: 1.49-1.61 (2H, m), 1.70-1.90 (8H, m), 2.04 (3H, s), 2.68 (2H, t, J=7.2 Hz), 3.19-3.23 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.09 (2H, t, J=6.6 Hz), 4.26 (1H, brs), 6.74-6.79 (3H, m), 7.18-7.30 (7H, m), 7.52-7.56 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 676(3) and methyl chloroglyoxylate; Yield: 85% (colorless oil).
1H-NMR (CDCl3) δ: 1.49-1.88 (10H, m), 2.05 (3H, s), 2.58-2.63 (2H, m), 3.47-3.56 (4H, m), 3.95-4.11 (5H, m), 6.99 (1H, d, J=8.7 Hz), 7.10-7.16 (3H, m), 7.20-7.22 (2H, m), 7.24-7.29 (2H, m), 7.32 (1H, d, J=2.4 Hz), 7.46-7.52 (3H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 676(4); Yield: 85% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 1.43-1.60 (8H, m), 1.69-1.74 (2H, m), 2.49-2.59 (2H, m), 3.38-3.52 (3H, m), 3.84-4.10 (3H, m), 7.11-7.13 (3H, m), 7.18-7.22 (3H, m), 7.43-7.48 (3H, m), 7.65-7.71 (3H, m), 13.58 (1H, brs).
Minor isomer: 1H-NMR (DMSO-d6) δ: 1.43-1.60 (8H, m), 1.69-1.74 (2H, m), 2.49-2.59 (2H, m), 3.38-3.62 (3H, m), 3.84-4.38 (3H, m), 7.08-7.13 (3H, m), 7.18-7.22 (3H, m), 7.43-7.48 (3H, m), 7.65-7.76 (3H, m), 13.58 (1H, brs).
The title compound was obtained in the same manner as the Example 185(2) using the following starting materials.
Starting materials: 4-bromo-1-fluoro-2-nitrobenzene and 1-pentanol; Yield: 69% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.34-1.49 (4H, m), 1.79-1.86 (2H, m), 4.08 (2H, t, J=6.6 Hz), 6.96 (1H, d, J=9.0 Hz), 7.60 (1H, dd, J=2.7, 9.0 Hz), 7.95 (1H, d, J=2.7 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 677(1) and 4-methylbenzeneboronic acid; Yield: 90% (yellow solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.34-1.50 (4H, m), 1.81-1.91 (2H, m), 2.40 (3H, s), 4.13 (2H, t, J=6.6 Hz), 7.12 (1H, d, J=8.7 Hz), 7.24-7.27 (2H, m), 7.43-7.47 (2H, m), 7.71 (1H, dd, J=2.4, 8.7 Hz), 8.04 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 677(2); Yield: 96% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.36-1.50 (4H, m), 1.81-1.91 (2H, m), 2.37 (3H, s), 3.86 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.82 (1H, d, J=8.4 Hz), 6.91-6.96 (2H, m), 7.19-7.21 (2H, m), 7.41-7.44 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 677(3) and 4-phenylbutyl bromide; Yield: 93% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.36-1.50 (4H, m), 1.51-1.88 (6H, m), 2.37 (3H, s), 2.64-2.71 (2H, m), 3.19-3.24 (2H, m), 4.00 (2H, t, J=6.6 Hz), 4.24 (1H, brs), 6.78-6.84 (3H, m), 7.11-7.30 (7H, m), 7.43-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 677(4) and methyl chloroglyoxylate; Yield: 75% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.36-1.50 (4H, m), 1.57-1.88 (6H, m), 2.39 (3H, s), 2.56-2.64 (2H, m), 3.52-3.60 (4H, m), 3.96-4.02 (3H, m), 6.96 (1H, d, J=8.7 Hz), 7.10-7.16 (3H, m), 7.20-7.25 (4H, m), 7.33 (1H, d, J=2.4 Hz), 7.37-7.40 (2H, m), 7.51 (1H, dd, J=2.4, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 677(5); Yield: 69% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.91 (3H, m), 1.36-1.52 (8H, m), 1.65-1.74 (2H, m), 2.33 (3H, s), 2.56-2.64 (2H, m), 3.13-4.04 (4H, m), 7.07-7.25 (8H, m), 7.41-7.46 (4H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.91 (3H, m), 1.36-1.52 (8H, m), 1.65-1.74 (2H, m), 2.33 (3H, s), 2.56-2.64 (2H, m), 3.13-4.04 (4H, m), 7.02-7.25 (8H, m), 7.41-7.51 (4H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 677(1) and 4-isopropylbenzeneboronic acid; Yield: 100% (yellow oil).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.29 (6H, d, J=6.9 Hz), 1.38-1.51 (4H, m), 1.81-1.90 (2H, m), 2.92-2.99 (1H, m), 4.13 (2H, t, J=6.6 Hz), 7.12 (1H, d, J=8.7 Hz), 7.30-7.34 (2H, m), 7.46-7.50 (2H, m), 7.71 (1H, dd, J=2.4, 8.7 Hz), 8.04 (1H, d, J=2.4 Hz).
The title compound was obtained in the same manner as the Example 125(2) using the following starting material.
Starting material: the intermediate 678(1); Yield: 85% (white solid).
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.28 (6H, d, J=6.9 Hz), 1.38-1.51 (4H, m), 1.79-1.88 (2H, m), 2.90-2.96 (1H, m), 3.86 (2H, brs), 4.02 (2H, t, J=6.6 Hz), 6.82 (1H, d, J=8.4 Hz), 6.91-6.96 (2H, m), 7.24-7.29 (2H, m), 7.44-7.48 (2H, m).
The title compound was obtained in the same manner as the Example 123(1) using the following starting materials.
Starting materials: the intermediate 678(2) and 4-phenylbutyl bromide; Yield: 89% (yellow oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.28 (6H, d, J=6.9 Hz), 1.36-1.50 (4H, m), 1.51-1.88 (6H, m), 2.64-2.71 (2H, m), 2.92-2.99 (1H, m), 3.19-3.24 (2H, m), 4.00 (2H, t, J=6.6 Hz), 4.24 (1H, brs), 6.78-6.84 (3H, m), 7.11-7.30 (7H, m), 7.43-7.46 (2H, m).
The title compound was obtained in the same manner as the Example 125(3) using the following starting materials.
Starting materials: the intermediate 678(3) and methyl chloroglyoxylate; Yield: 79% (colorless oil).
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.2 Hz), 1.28 (6H, d, J=6.9 Hz), 1.36-1.50 (4H, m), 1.51-1.88 (6H, m), 2.64-2.71 (2H, m), 2.92-2.99 (1H, m), 3.52-3.60 (4H, m), 3.96-4.02 (3H, m), 6.96 (1H, d, J=8.7 Hz), 7.10-7.16 (3H, m), 7.20-7.25 (2H, m), 7.28-7.31 (2H, m), 7.34 (1H, d, J=2.7 Hz), 7.41-7.44 (2H, m), 7.51 (1H, dd, J=2.7, 8.7 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 678(4); Yield: 62% (white solid).
This compound was obtained as a mixture of the rotational isomers.
Major isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.91 (3H, m), 1.23 (6H, d, J=6.9 Hz), 1.33-1.52 (8H, m), 1.65-1.74 (2H, m), 2.56-2.64 (2H, m), 2.87-2.96 (1H, m), 3.13-4.04 (4H, m), 7.07-7.19 (6H, m), 7.28-7.30 (2H, m), 7.44-7.49 (4H, m).
Minor isomer: 1H-NMR (DMSO-d6) δ: 0.84-0.91 (3H, m), 1.23 (6H, d, J=6.9 Hz), 1.33-1.52 (8H, m), 1.65-1.74 (2H, m), 2.56-2.64 (2H, m), 2.87-2.96 (1H, m), 3.13-4.04 (4H, m), 7.03-7.23 (6H, m), 7.29-7.32 (2H, m), 7.44-7.51 (4H, m).
A mixture of the intermediate 125(2) (500 mg, 1.97 mmol), 4-(tert-butyl)cyclohexanecarboxylic acid (mixture of cis- and trans-) (800 mg, 4.34 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (909 mg, 4.74 mmol) and chloroform (20 ml) was stirred at room temperature for 5 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (618 mg, 75%) as a white solid.
1H-NMR (CDCl3) δ: 0.84 (9H, s), 1.00-1.08 (2H, m), 1.21-1.42 (2H, m), 1.56-1.71 (3H, m), 2.21-2.26 (2H, m), 2.62-2.72 (1H, m), 7.25-7.28 (3H, m), 7.38 (1H, brs), 7.49-7.64 (5H, m).
A solution of the intermediate 679(1) (313 mg, 0.746 mmol) in anhydrous tetrahydrofuran (2 ml) was added dropwise to a suspension of lithium aluminium hydride (141 mg, 3.730 mmol) in anhydrous tetrahydrofuran (3 ml) under reflux, and the mixture was stirred for 2 hours. The reaction mixture was cooled to 0° C., followed by addition of 2 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=20:1) to give the title compound (258 mg, 85%) as a white solid.
1H-NMR (CDCl3) δ: 0.85 (9H, s), 0.98-1.14 (4H, m), 1.15-1.57 (3H, m), 1.84-1.86 (2H, m), 1.98-2.19 (1H, m), 3.19 (2H, d, J=7.5 Hz), 3.79 (1H, brs), 6.64-6.70 (2H, m), 7.21-7.23 (2H, m), 7.35-7.43 (2H, m), 7.50-7.55 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 679(2) and methyl chloroglyoxylate; Yield: 90% (colorless oil).
1H-NMR (CDCl3) δ: 0.85 (9H, s), 0.90-1.02 (1H, m), 1.19-1.33 (3H, m), 1.38-1.49 (3H, m), 1.55-1.69 (2H, m), 1.81-1.93 (1H, m), 3.58 (3H, s), 3.92 (2H, d, J=8.1 Hz), 7.27-7.32 (4H, m), 7.55-7.62 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 679(3); Yield: 81% (white solid).
1H-NMR (DMSO-d6) δ: 0.83 (9H, s), 0.90-1.02 (1H, m), 1.23-1.25 (2H, m), 1.31-1.40 (2H, m), 1.47-1.72 (5H, m), 3.87 (2H, d, J=7.5 Hz), 7.41-7.48 (4H, m), 7.75-7.84 (4H, m), 13.90 (1H, brs).
The title compound was obtained in the same manner as the Example 679(1) using the following starting materials.
Starting materials: the intermediate 125(2) and 4-(tert-butyl)cyclohexanecarboxylic acid (mixture of cis- and trans-); Yield: 25% (white solid).
1H-NMR (CDCl3) δ: 0.97 (9H, s), 1.04-1.10 (3H, m), 1.44-1.72 (3H, m), 1.83-2.00 (2H, m), 2.00-2.10 (1H, m), 2.11-2.30 (1H, m), 7.25-7.28 (3H, m), 7.49-7.63 (6H, m).
The title compound was obtained in the same manner as the Example 679(2) using the following starting material.
Starting material: the intermediate 680(1); Yield: 100% (white solid).
1H-NMR (CDCl3) δ: 0.85 (9H, s), 0.93-1.04 (5H, m), 1.45-1.61 (1H, m), 1.78-2.05 (5H, m), 2.99 (2H, d, J=6.6 Hz), 6.65-6.70 (2H, m), 7.21-7.24 (2H, m), 7.36-7.44 (2H, m), 7.50-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(2) using the following starting materials.
Starting materials: the intermediate 680(2) and methyl chloroglyoxylate; Yield: 92% (colorless oil).
1H-NMR (CDCl3) δ: 0.81 (9H, s), 0.87-1.09 (4H, m), 1.43-1.59 (2H, m), 1.71-1.92 (4H, m), 3.58 (3H, s), 3.69 (2H, d, J=7.5 Hz), 7.27-7.34 (4H, m), 7.56-7.63 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 680(3); Yield: 87% (yellow oil).
1H-NMR (DMSO-d6) δ: 0.79 (9H, s), 0.82-0.93 (4H, m), 1.25-1.40 (3H, m), 1.71-1.82 (3H, m), 3.63 (2H, d, J=7.2 Hz), 7.39-7.51 (4H, m), 7.68-7.84 (4H, m), 14.13 (1H, brs).
The title compound was obtained in the same manner as the Example 679(1) using the following starting materials.
Starting materials: the intermediate 3-bromoaniline and 4-phenylbutyric acid; Yield: 90% (white solid).
1H-NMR (CDCl3) δ: 2.00-2.15 (2H, m), 2.34 (2H, t, J=7.5 Hz), 2.71 (2H, t, J=7.5 Hz), 7.06 (1H, brs), 7.12-7.43 (8H, m), 7.71-7.81 (1H, m).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 681(1) and ethyl bromoacetate; Yield: 40% (pale yellow oil).
1H-NMR (CDCl3) δ: 1.28 (3H, t, J=7.2 Hz), 1.83-1.90 (2H, m), 2.14 (2H, t, J=7.5 Hz), 2.57 (2H, t, J=7.5 Hz), 4.20 (2H, q, J=7.2 Hz), 4.32 (2H, s), 7.03-7.33 (7H, m), 7.42-7.54 (2H, m).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 681(2) and 4-(trifluoromethoxy)phenylboronic acid; Yield: 67% (colorless oil).
1H-NMR (CDCl3) δ: 1.27 (3H, t, J=7.2 Hz), 1.85-2.02 (2H, m), 2.20 (2H, t, J=7.2 Hz), 2.58 (2H, t, J=7.2 Hz), 4.21 (2H, q, J=7.2 Hz), 4.39 (2H, s), 7.03-7.35 (8H, m), 7.40-7.60 (5H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 681(3); Yield: 53% (pale black solid).
1H-NMR (CDCl3) δ: 1.60-1.88 (2H, m), 1.88-2.20 (2H, m), 2.20-2.53 (2H, m), 4.19 (2H, s), 6.73-7.61 (13H, m), 10.05 (1H, brs).
The title compound was obtained in the same manner as the Example 679(1) using the following starting materials.
Starting materials: the intermediate 194(2) and 4-phenylbutyric acid; Yield: 63.7% (white solid).
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.2 Hz), 1.39-1.50 (4H, m), 1.81-1.89 (2H, m), 2.05-2.13 (2H, m), 2.42 (2H, t, J=7.2 Hz), 2.74 (2H, t, J=7.2 Hz), 4.07 (2H, t, J=6.6 Hz), 6.92 (1H, d, J=8.4 Hz), 7.19-7.30 (8H, m), 7.58-7.61 (2H, m), 7.78 (1H, brs), 8.69 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 125(4) using the following starting materials.
Starting materials: the intermediate 682(1) and ethyl bromoacetate; Yield: 37% (colorless oil).
1H-NMR (CDCl3) δ: 0.92 (3H, t, J=6.9 Hz), 1.20-1.50 (7H, m), 1.67-2.30 (6H, m), 2.56 (2H, t, J=6.6 Hz), 3.63 (1H, d, J=17.1 Hz), 3.99 (2H, t, J=6.6 Hz), 4.08-4.30 (2H, m), 5.05 (1H, d, J=17.1 Hz), 6.99 (1H, d, J=9.0 Hz), 7.04-7.22 (5H, m), 7.22-7.33 (2H, m), 7.45-7.56 (3H, m), 7.66 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 682(2); Yield: 100% (colorless oil).
1H-NMR (CDCl3) δ: 0.82-0.97 (3H, m), 1.21-1.46 (4H, m), 1.62-1.92 (4H, m), 1.96-2.24 (2H, m), 2.47 (2H, t, J=7.5 Hz), 3.69 (1H, d, J=16.8 Hz), 3.85-4.02 (2H, m), 4.81 (1H, d, J=16.8 Hz), 6.90-7.24 (8H, m), 7.40-7.52 (3H, m), 7.58 (1H, d, J=2.1 Hz).
The title compound was obtained in the same manner as the Example 123(3) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-(2-calboxyethyl)phenylboronic acid; Yield: 36% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.72 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 3.57 (3H, s), 4.94 (2H, s), 7.11-7.20 (4H, m), 7.25-7.34 (4H, m), 7.47-7.54 (4H, m).
The title compound was obtained in the same manner as the Example 126(4) using the following starting material.
Starting material: the intermediate 683(1); Yield: 83% (pale yellow oil).
1H-NMR (DMSO-d6) δ: 1.25 (9H, s), 2.56 (2H, t, J=7.5 Hz), 2.85 (2H, t, J=7.5 Hz), 4.93 (2H, s), 7.16 (2H, d, J=8.4 Hz), 7.26-7.36 (6H, m), 7.56 (2H, d, J=8.4 Hz), 7.65 (2H, d, J=8.4 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-acetylphenylboronic acid; Yield: 50% (white solid).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 2.64 (3H, s), 3.60 (3H, s), 4.96 (2H, s), 7.19 (4H, d, J=8.1 Hz), 7.32 (2H, d, J=8.1 Hz), 7.58 (2H, d, J=8.1 Hz), 7.65 (2H, d, J=8.1 Hz), 8.03 (2H, d, J=8.1 Hz).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 684(1); Yield: 62% (pale yellow solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 2.60 (3H, s), 4.92 (2H, s), 7.06-7.35 (4H, m), 7.39 (2H, d, J=8.5 Hz), 7.67 (2H, d, J=8.5 Hz), 7.79 (2H, d, J=8.5 Hz), 8.01 (2H, d, J=8.5 Hz).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-N-(methanesulfonamide)phenylboronic acid; Yield: 30% (colorless oil).
1H-NMR (CDCl3) δ: 1.30 (9H, s), 3.05 (3H, s), 3.58 (3H, s), 4.94 (2H, s), 6.88 (1H, s), 7.10-7.23 (4H, m), 7.26-7.39 (4H, m), 7.45-7.62 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 685(1); Yield: 35% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 3.01 (3H, s), 4.91 (2H, s), 7.05-7.44 (8H, m), 7.50-7.73 (4H, m), 9.90 (1H, s).
The title compound was obtained in the same manner as the Example 1(2) using the following starting materials.
Starting materials: the intermediate 126(2) and 4-hydroxyphenylboronic acid; Yield: 37% (white solid).
1H-NMR (CDCl3) δ: 1.29 (9H, s), 3.57 (3H, s), 4.94 (2H, s), 6.59 (1H, s), 6.83-6.94 (2H, m), 7.06-7.14 (2H, m), 7.15-7.24 (2H, m), 7.28-7.36 (2H, m), 7.37-7.50 (4H, m).
The title compound was obtained in the same manner as the Example 12(4) using the following starting material.
Starting material: the intermediate 686(1); Yield: 63% (white solid).
1H-NMR (DMSO-d6) δ: 1.24 (9H, s), 4.85 (2H, s), 6.79 (2H, d, J=8.2 Hz), 7.06-7.53 (10H, m).
In a 96-well multiplate (black), 1.5 μl of DMSO solution of the compound according to the present invention, which had been prepared to achieve 80-fold the test concentration (=the final concentration when fluorogenic substrate is added), was diluted with 52.5 μl of pH 7.5 Tris buffer. To this solution, 6 μl of 80 nM recombinant human PAI-1 (Molecular Innovations, Inc.) solution prepared with Tris buffer was added, and the plate was incubated for 5 minutes at room temperature. Furthermore, 30 μl of 800 IU/ml two-chain tPA (Activity Standard; American diagnostica, inc.) prepared with Tris buffer was added, and the mixed solution was incubated for 15 minutes at room temperature. Then, 30 μl of 400 μM fluorogenic substrate (Pyr-Gly-Arg-MCA; Peptide Institute, Inc.) for tPA prepared with Tris buffer was added and reacted for 30 minutes at room temperature. Every 5 minutes from the reaction start, fluorescence (excitation wavelength=360 nm, emission wavelength=465 nm) was measured using SPECTRAFLUOR (TECAN G.M.B.H.) or GENios (TECAN G.M.B.H.), and intensity of fluorescence increased by 30 minute reaction were measured. The increments of fluorescence by 30 minutes reaction in the presence or absence (tPA alone) of PAI-1 in the control wells (DMSO) were calculated respectively, and their differences ([data in the absence of PAI-1]−[data in the presence of PAI-1]) being 100% of PAI-1 activity, the inhibition rates of PAI-1 activity in the presence of the compound according to the present invention were calculated.
50 mM Tris, 150 mM NaCl, 10 μg/ml BSA, 0.01% Tween80 (SIGMA-ALDRICH Corporation)
In the following, inhibition rates of human PAI-1 activity are shown. “NT” on the table means that the measurement was not carried out.
Except using the pH 7.4 HEPES buffer instead of the pH 7.5 Tris buffer, and the change of incubation time from 15 minutes to 10 minutes of the mixed solution added to two-chain tPA solution, tests were carried out in the same manner as the Test Example 1.
0.1 M HEPES, 0.1 M NaCl. 1 mM EDTA. 0.1% Polyethylene glycol 8,000 (Hampton Research Corporation),
2 mM Dimethyldecylphoshine oxide [Apo-10] (Fluka Corporation)
In the following, inhibition rates of human PAI-1 activity are shown.
From the above results, concentrations of the present application compounds that inhibit 50% of the human PAI-1 activity (IC50) were calculated. The results are shown on the following tables.
Except using recombinant rat PAI-1 (Molecular Innovations, Inc) instead of recombinant human PAI-1, tests were carried out in the same manner as the Test Example 2.
In the following, inhibition rates of rat PAI-1 activity are shown.
From the above results, concentrations of the present application compounds that inhibit 50% of the rat PAI-1 activity (IC50) were calculated. The results are shown on the following table.
100 μl of tPA solution, where one-chain recombinant tPA (hereinafter referred to as tPA; American diagnostica, inc.) had been diluted with Buffer A to achieve a concentration of 10 μg/ml, was added to each well of a 96-well plate (Nunc Maxisorp), and the plate was incubated for one night at 4° C. to be coated with tPA. Then, after suction of tPA solution from the 96-well plate, the plate was rinsed successively with Buffer A and Buffer B.
To Buffer B, solutions of the compound according to the present invention dissolved with DMSO (final DMSO concentration: 0.2%) and recombinant human PAI-1 (Molecular Innovations, Inc.) were added. The mixtures were blended so that the final concentrations would be 0.1 to 3.0 μM and 50 ng/ml respectively, and were incubated for 15 minutes on ice. These mixed solutions were added to the rinsed 96-well plate at 100 μl/well, and incubated for 60 minutes at room temperature. To prepare a calibration curve, PAI-1 solutions without the compound according to the present invention (solutions where the final concentrations being 100, 50, 25, 12.5, 6.25, 3.13, or 1.56 ng/ml PAI-1) were added at 100 μl/well, and the plate was incubated for 60 minutes at room temperature, as standard.
After incubation, the reaction mixture was removed by suction, and each well was rinsed with Wash Buffer. Next, anti-human PAI-1 monoclonal antibody (PROGEN Inc.) diluted with Buffer C to be 3.0 μg/ml was added to the 96-well plate at 100 μl/well, and the plate was incubated for 1 hour at room temperature. After rinsing each well with Wash Buffer, alkaline phosphatase-labeled goat anti-mouse IgG (H+L) (Jackson ImmunoResearch, Inc.) diluted with Buffer D to be 0.12 μg/ml was added at 100 μl/well, and the plate was incubated for 1 hour at room temperature. After rinsing each well with Wash Buffer, 1.0 mg/ml p-Nitrophenyl Phosphate (SIGMA) was added to the 96-well plate at 100 μl/well to start the reaction. After 30 to 60 minutes, 25 μl of 0.5 N NaOH was added to stop the reaction, and the absorbance was measured at 405 nm using a multiplate reader (GENios; TECAN G.M.B.H.). Based on the calibration curve prepared from the standard wells, amounts of PAI-1 bound to tPA in the wells that had been treated with the compound according to the present invention were calculated, and the PAI-1 inhibition rates by the compounds according to the present invention were obtained by the following equation. [PAI-1 Inhibition Rate (%)]=[1−(amount of PAI-1 bound to tPA on the well by treatment with the compound according to the present invention)/(amount of PAI-1 bound to tPA on the well by treatment with PAI-1 solution not including the compound according to the present invention (solution having the final concentration of 50 ng/ml PAI-1)]×100
50 mM sodium phosphate, 0.1 M NaCl, 1 mM EDTA, pH 6.6
50 mM sodium phosphate, 100 mM NaCl, pH 7.4
<Composition of p-Nitrophenyl Phosphate Solution>
0.5 mM MgCl2, p-Nitrophenyl phosphate, pH 9.8
In the following, inhibition rates of human PAI-1 activities are shown.
AV shunt model using 7-week old male Crlj: CD (SD) rats were prepared, and anti thrombotic activities when the compounds according to the present invention were administered orally were examined.
Required amount of the test compounds were weighed and suspended by adding 0.5% CMC (carboxymethylcellulose)-Na solution little by little, and the solutions (10 mg/kg or 30 mg/kg solution) were prepared so that their final concentration became 2 mg/ml or 6 mg/ml using a graduated cylinder. 5 ml was prepared for 1 course.
To 7-week old Crlj: CD (SD) male rats, 5 ml/kg of vehicle (0.5% CMC-Na solution) or 5 ml/kg of the administering solution of the test compound (10 mg/kg or 30 mg/kg) were administered orally for 4 days. The administration on the 4th day was carried out about 1 hour before the following perfusion start.
A 6.5 cm silk thread (Matsuda Ika Kogyou; No. 1-0) was put through in an 8 cm No. 7 polyethylene tube (Hibiki), and No. 3 tubes (12.5 cm) were connected to both of the ends via No. 5 tube (1.5 cm), to prepare a catheter for shunt. On the connected part where the silk thread was through, parafilm was wrapped around to avoid blood leakage.
Rats were anesthetized with pentobarbital (50 mg/kg; intraperitoneally). Saline was filled in the above catheter, and each of the ends of the catheter was inserted in right carotid artery and left carotid artery, respectively, and blood was circulated. 30 minutes later, the catheter was pinched with forceps to stop blood flow, and tube parts where the silk thread was through were cut and removed. The silk thread was carefully removed from the tubes, remaining wet weight was weighed after removing the liquid phase with filter paper, and further subtraction of the weight of the silk thread, gave the thrombus weight.
For the thrombus weight in each group, an average value ±standard error (S.E.) was calculated. For the significance test between the vehicle administered group and the compound according to the present invention administered group, Dunnett's multiple comparison was carried out (significance level 5%). For the test, the SAS System Release 8.2 (TS2M0) for Windows (Registered Trademark) (SAS Institute Inc.) and its cooperative system EXSAS Ver. 7.10 (Arm Systex Co. Ltd.) were employed.
Number | Date | Country | |
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61044108 | Apr 2008 | US |