Patent Application
20240132519
The present invention relates to an Nrf2-activating compound.
Nrf2 (NF-E2-related factor 2) is a transcription factor that promotes the expression of oxidative-stress defense genes. Due to its interaction with Keap1 (Kelch-like ECH-associated protein 1), Nrf2 undergoes ubiquitylation and proteasomal degradation. This prevents the interaction between Nrf2 and Keap1 and thus promotes the translocation of Nrf2 into the nucleus, thereby activating the expression of oxidative-stress defense genes. For example, Nrf2 activators are expected to be a therapeutic agent for diseases in the systemic area, such as multiple sclerosis, psoriasis, and diabetic nephropathy, and for diseases in the ophthalmic area, such as dry eyes, diabetic retinopathy, retinitis pigmentosa, and glaucoma.
Patent Literature 1 discloses an Nrf2 activator intended mainly for use in the treatment of chronic obstructive pulmonary disease (COPD).
An object of the present invention is to provide a compound having Nrf2-activating action.
The present inventors conducted extensive research to achieve the object, and found that the compound represented by formula (I), described later, or the compounds of the less-polar group of two groups of diastereomers, described later, in which the carbon atom indicated by * in formula (II) is an asymmetric carbon atom, salts of the compounds, and solvates of the compounds or salts have Nrf2-activating action. They conducted further research based on this finding and completed the present invention.
Specifically, the present invention includes the following subject matter.
A compound represented by formula (I), a salt of the compound, or a solvate of the compound or salt:
A compound that is the less-polar of two diastereomers in which the carbon atom indicated by * in formula (II) is an asymmetric carbon atom:
The compound according to Item 2, a salt of the compound, or a solvate of the compound or salt, wherein the compound is a compound that is first eluted when an isomer mixture containing two diastereomers in which the carbon atom indicated by * in the formula is an asymmetric carbon atom and in which the configuration of R6 is fixed is subjected to column separation (column type: CHIRAL ART Cellulose-SC, and elution solvent: 40/60/0.1 mixed solvent of n-hexane/ethanol/trifluoroacetic acid).
The compound according to any one of Items 1 to 3, a salt of the compound, or a solvate of the compound or salt, wherein the optional substituent of the thienyl group includes an electron-withdrawing group.
The compound according to any one of Items 1 to 4, a salt of the compound, or a solvate of the compound or salt, wherein the optional substituent of the thienyl group includes an acetyl group, a sulfamoyl group, a cyano group, or cycloalkanecarbonyl.
The compound according to any one of Items 1 to 5, a salt of the compound, or a solvate of the compound or salt, wherein R2 is a group represented by formula (R2Aa) or (R2Ab):
The compound according to Item 6, a salt of the compound, or a solvate of the compound or salt, wherein R3 is an acetyl group.
The compound according to Item 6 or 7, a salt of the compound, or a solvate of the compound or salt, wherein R4 and R5 are identical or different and represent a hydrogen atom or an alkyl group.
The compound according to any one of Items 1 to 8, a salt of the compound, or a solvate of the compound or salt, wherein R2 is represented by formula (R2Aa):
A compound of any of the following, a salt of the compound, or a solvate of the compound or salt:
A compound (compound D1) that is first eluted when 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoic acid is subjected to column separation (column type: CHIRAL ART Cellulose-SC, and elution solvent: 40/60/0.1 mixed solvent of n-hexane/ethanol/trifluoroacetic acid),
A medicament comprising at least one member selected from the group consisting of the compound of any one of Items 1 to 9, 9a, and 9b, a salt of the compound, and a solvate of the compound or salt.
The medicament according to Item 10, which is an Nrf2 (NF-E2-related factor 2) activator.
The medicament according to Item 10 or 11, which is a topically administered formulation.
The medicament according to any one of Items 10 to 12, which is an ophthalmic formulation.
The medicament according to Item 10 or 11, which is a parenterally administered formulation.
The medicament according to Item 10, 11, or 14, which is an intravenously administered formulation.
The medicament according to any one of Items 10 to 15, which is a medicament for prevention or treatment of a brain disease, a lung disease, a skin disease, an otologic disease, a kidney disease, or an ophthalmic disease.
A method for preventing or treating a disease in which Nrf2 participates, comprising administering at least one member selected from the group consisting of the compound of any one of Items 1 to 9, 9a, and 9b, a salt of the compound, and a solvate of the compound or salt to a patient.
The method according to Item 17, wherein the patient has a disease in which Nrf2 participates.
The method according to Item 17 or 17a, wherein the disease is a brain disease, a lung disease, a skin disease, an otologic disease, a kidney disease, or an ophthalmic disease.
At least one substance selected from the group consisting of the compound of any one of Items 1 to 9, 9a, and 9b, a salt of the compound, and a solvate of the compound or salt, for use in a medicament.
At least one substance selected from the group consisting of the compound of any one of Items 1 to 9, 9a, and 9b, a salt of the compound, and a solvate of the compound or salt, for use in the prevention or treatment of a disease in which Nrf2 participates.
The substance for use according to Item 19, wherein the disease is a brain disease, a lung disease, a skin disease, an otologic disease, a kidney disease, or an ophthalmic disease.
Use of at least one substance selected from the group consisting of the compound of any one of Items 1 to 9, 9a, and 9b, a salt of the compound, and a solvate of the compound or salt, in the production of a medicament.
The use according to Item 20, wherein the medicament is an Nrf2 (NF-E2-related factor 2) activator.
The use according to Item 20 or 20a, wherein the medicament is a medicament for prevention or treatment of a brain disease, a lung disease, a skin disease, an otologic disease, a kidney disease, or an ophthalmic disease.
The present invention provides a compound having an Nrf2-activating action, a salt of the compound, and a solvate of the compound or salt. The present invention also provides a medicament containing at least one member selected from the compound, the salt, or the solvate; more specifically, the present invention provides a medicament such as an Nrf2 activator, a topically administered formulation, and a medicament for prevention or treatment of a brain disease, a lung disease, a skin disease, an otologic disease, a kidney disease, an ophthalmic disease, or the like.
In the present specification, the expressions “comprising,” “including,” and “containing” include the concepts of “comprising,” “containing,” “consisting essentially of,” and “consisting of.”
In an embodiment, the present invention relates to a compound represented by formula (I):
a salt of the compound, or a solvate of the compound or salt.
In an embodiment, the present invention also relates to a compound that is the less-polar of two diastereomers in which the carbon atom indicated by * in formula (II) is an asymmetric carbon atom:
a salt of the compound, or a solvate of the compound or salt.
These compounds are described below. In the present specification, these compounds may be collectively referred to as “the compound of the present invention.”
1-1. R1, R1a, and R1b
R1 represents an alkyl group.
The alkyl group represented by R1 includes both a linear alkyl group and a branched alkyl group (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 4, preferably 1 to 3, more preferably 1 to 2, and still more preferably 1. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, and a sec-butyl group.
R1a and R1b each represents an alkyl group.
Examples of the alkyl group represented by R1a or R1b include those mentioned as examples of the alkyl group represented by R1. R1a and R1b are generally identical. In a particularly preferable embodiment of the present invention, R1a and R1b are both methyl groups.
R2 represents an optionally substituted thienyl group.
Examples of thienyl groups include a 2-thienyl group, a 3-thienyl group, and the like, among which a 2-thienyl group is preferred.
Examples of substituents of the optionally substituted thienyl group include acyl groups, such as an acetyl group and a cycloalkanecarbonyl group, a sulfamoyl group, a cyano group, —R21—NR22R23 (R21 represents a single bond, a carbonyl group, or an alkylene group; R22 and R23 are identical or different and represent a hydrogen atom, an optionally substituted alkyl group, or R22 and R23 bind with each other to form an alkylene group and form a ring together with an adjacent nitrogen atom), an alkoxy group, a halogen atom, and an alkyl group. The substituent can be at any position, and is, for example, at any ring-constituting atom of a thiophene ring (a carbon atom or a sulfur atom), preferably at a carbon atom of a thiophene ring. The number of substituents is not particularly limited, and can be, for example, 0 to 4, preferably 0 to 2, and more preferably 1 to 2.
The acyl group as a substituent of the optionally substituted thienyl group can be any acyl group that is formed by removing a hydroxy group from a carboxylic acid, and is preferably a group represented by —CO—R24 (R24 represents an alkyl group or a cycloalkyl group, preferably an alkyl group). The alkyl group represented by R24 includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, a sec-butyl group, an n-pentyl group, a neopentyl group, an n-hexyl group, and a 3-methyl pentyl group. The number of carbon atoms of the cycloalkyl group represented by R24 is not particularly limited, and is, for example, 3 to 8, preferably 3 to 6, more preferably 3 to 4, and still more preferably 3. The acyl group as a substituent is preferably, for example, an acetyl group, and a cycloalkanecarbonyl group; from the standpoint of Nrf2-activating action, the acyl group as a substituent is particularly preferably an acetyl group.
R21 of —R21—NR22R23 as a substituent of the optionally substituted thienyl group represents a single bond, a carbonyl group, or an alkylene group (preferably a carbonyl group). The alkylene group represented by R21 includes both linear alkylene groups and branched alkylene groups (preferably a linear alkylene group). The number of carbon atoms of the alkylene group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkylene group include a methylene group, an ethylene group, a propylene group, and a butylene group. R22 and R23 of —R21—NR22R23 as a substituent are identical or different and represent a hydrogen atom, an optionally substituted alkyl group, or R22 and R23 bind with each other to form an alkylene group and form a ring together with an adjacent nitrogen atom (preferably R22 and R23 are identical or different and represent a hydrogen atom or an alkyl group, more preferably one of R22 and R23 is a hydrogen atom and the other is an alkyl group, and still more preferably R22 and R23 both are a hydrogen atom). The alkyl group represented by R22 or R23 includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, a sec-butyl group, an n-pentyl group, an neopentyl group, an n-hexyl group, and a 3-methyl pentyl group. The substituent of the optionally substituted alkyl group is, for example, an alkoxy group. The alkoxy group includes both linear alkoxy groups and branched alkoxy groups (preferably a linear alkoxy group). The number of carbon atoms of the alkoxy group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, an isobutoxy group, a sec-butoxy group, and a tert-butoxy group.
The alkoxy group as a substituent of the optionally substituted thienyl group includes both linear alkoxy groups and branched alkoxy groups (preferably a linear alkoxy group). The number of carbon atoms of the alkoxy group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, an isobutoxy group, a sec-butoxy group, and a tert-butoxy group.
The halogen atom as a substituent of the optionally substituted thienyl group is, for example, a fluorine atom, a chlorine atom, a bromine atom, or an iodine atom, preferably a fluorine atom, or a chlorine atom, and more preferably a fluorine atom.
The alkyl group as a substituent of the optionally substituted thienyl group includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 4, preferably 1 to 3, more preferably 1 to 2, and still more preferably 1. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, and a sec-butyl group.
In a preferable embodiment of the present invention, it is preferred that the substituent of the optionally substituted thienyl group preferably contains an electron-withdrawing group (i.e., when the number of substituents is one, the substituent is an electron-withdrawing group, and when the number of substituents is two or more, at least one substituent is an electron-withdrawing group). More preferably, the substituent of the optionally substituted thienyl group is an acyl group, a sulfamoyl group, or a cyano group (still more preferably an acetyl group, a sulfamoyl group, a cyano group, or a cycloalkanecarbonyl group; particularly from the standpoint of Nrf2-activating action, particularly preferably an acetyl group) (i.e., when the number of substituents is one, the substituent is any one of these groups, and when the number of substituents is two or more, at least one substituent is any of these groups). In these embodiments, preferably, the number of substituents of the group derived from a heterocycle is 0 to 2 (preferably 1 to 2). When the number of substituents is two or more, at least one substituent is an alkyl group, a halogen atom, or an alkoxy group (preferably an alkoxy group).
In a preferable embodiment of the present invention, R2 is preferably, for example, a group represented by formula (R2A):
The substituents represented by R3 and Y are as defined for the substituents of the optionally substituted thienyl group represented by R2.
R3 is preferably an acyl group (preferably, —CO—R24 (R24 represents an alkyl group or a cycloalkyl group)), a sulfamoyl group, or a cyano group, more preferably an acetyl group, a sulfamoyl group, a cyano group, or a cycloalkanecarbonyl group; particularly from the standpoint of Nrf2-activating action, R3 is particularly preferably an acetyl group.
1-3. R4 and R5
R4 and R5 are identical or different and represent a hydrogen atom or an optionally substituted alkyl group, or R4 and R5 bind with each other to form —NH—CH═N—.
The alkyl group represented by R4 or R5 includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 4, preferably 1 to 3, more preferably 1 to 2, and still more preferably 1. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, and a sec-butyl group.
The substituent of the optionally substituted alkyl group represented by R4 or R5 is, for example, a halogen atom. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The number of substituents is not particularly limited, and is, for example, 0 to 3, and preferably 0.
The phrase “R4 and R5 bind with each other to form —NH—CH═N—” means that the following moiety in formula (I)
takes the following structure.
In a preferable embodiment of the present invention, preferably, R4 and R5 are identical or different and represent a hydrogen atom or an alkyl group; more preferably, one of R4 and R5 is an alkyl group, and the other is a hydrogen atom; still more preferably, R4 is a hydrogen atom, and R5 is an alkyl group.
R6 represents an optionally substituted alkyl group.
The alkyl group represented by R6 includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 2. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, a sec-butyl group, an n-pentyl group, an neopentyl group, an n-hexyl group, and a 3-methyl pentyl group.
The substituent of the optionally substituted alkyl group represented by R6 is, for example, a hydroxyl group, an alkoxy group, an aryl alkoxy group, an aryloxy group, or —NR61R62 (R61 and R62 are identical or different and represent a hydrogen atom or an alkyl group). The position of the substituent is not particularly limited; in an embodiment of the present invention, the substituent is preferably at the terminal of the alkyl group. The number of substituents is not particularly limited, and is, for example, 0 to 3, and preferably 0 to 1.
The substituent of the alkoxy group includes both linear alkoxy groups and branched alkoxy groups (preferably a linear alkoxy group). The number of carbon atoms of the alkoxy group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 1. Specific examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, an isobutoxy group, a sec-butoxy group, and a tert-butoxy group.
The aryl alkoxy group as a substituent can be any alkoxy group substituted with an aryl group. The number of carbon atoms of the aryl group is not particularly limited, and is, for example, 6 to 14, and preferably 6 to 8. Specifically, such an aryl group is, for example, a phenyl group, a naphthyl group, a biphenyl group, a pentalenyl group, an indenyl group, an anthryl group, a tetracenyl group, a pentacenyl group, a pyrenyl group, a perylenyl group, a fluorenyl group, or a phenanthryl group, and particularly preferably a phenyl group. The position of substitution with the aryl group in the alkoxy group is not particularly limited; in an embodiment of the present invention, the position of substitution is preferably at the terminal of the alkoxy group. The aryl alkoxy group is, for example, a benzyloxy group, or a phenethyloxy group.
The number of carbon atoms of the aryloxy group as a substituent is not particularly limited, and is, for example, 6 to 14, and preferably 6 to 8. Specifically, the aryl group that constitutes the aryloxy group is, for example, a phenyl group, a naphthyl group, a biphenyl group, a pentalenyl group, an indenyl group, an anthranil group, a tetracenyl group, a pentacenyl group, a pyrenyl group, a perylenyl group, a fluorenyl group, or a phenanthryl group, and particularly preferably a phenyl group. The aryloxy group is, for example, a phenyloxy group.
R61 and R62 that constitute —NR61R62 as a substituent are identical or different, and represent a hydrogen atom or an alkyl group. The alkyl group represented by R61 or R62 includes both linear alkyl groups and branched alkyl groups (preferably a linear alkyl group). The number of carbon atoms of the alkyl group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 to 2, and particularly preferably 2. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a tert-butyl group, a sec-butyl group, an n-pentyl group, an neopentyl group, an n-hexyl group, and a 3-methyl pentyl group.
In a preferable embodiment of the present invention, R6 is preferably an alkyl group optionally substituted with a hydroxyl group, an alkoxy group, or an aryl alkoxy group, more preferably an alkyl group optionally substituted with an aryl alkoxy group, and still more preferably an alkyl group.
The configuration of R6 is not particularly limited, and can be configuration p:
or configuration q:
In a preferable embodiment of the present invention, the configuration of R6 is configuration p.
R7 represents a hydroxy group, a hydrolyzable group, or —NR71R72 (R71 and R72 are identical or different and represent a hydrogen atom or a —[C(═O)]0-1-hydrocarbon group.
The hydrolyzable group is not particularly limited as long as the ester bond formed with the carbonyl group adjacent to R7 is hydrolyzed (preferably under physiological conditions or by an enzyme such as an esterase) to form a hydroxy group. The hydrolyzable group is a group (—O—Rx wherein Rx is an arbitrary substituent) that forms an ester bond with the carbonyl group adjacent to R7. Specific examples thereof include an alkoxy group, an aryloxy group (aryl-O—), an arylalkoxy group (an alkoxy group substituted with an aryl group), an alkylaryloxy group (an aryloxy group substituted with an alkyl group), an aralkyloxy group (an alkoxy group substituted with an aryl group), an alkoxyalkoxy group (an alkoxy group substituted with an alkoxy group), an acyloxy group, and an acyloxyalkoxy group (an alkoxy group substituted with an acyloxy group).
The “—[C(═O)]0-1-hydrocarbon group” is “-hydrocarbon group” when [C(═O)]0 and “—C(═O)-hydrocarbon group” when [C(═O)]1.
The “hydrocarbon group” in the definition of R71 and R72 is not particularly limited, and typical examples include an alkyl group and an aryl group.
R7 is preferably a hydroxy group.
1-6. A1, A2, A3, and A4
A1, A2, A3, and A4 are identical or different and represent CH or N (however, the number of N is 1 or less).
When one of A1, A2, A3, and A4 is N, preferably A1 or A3 is N, and more preferably A3 is N.
In a preferable embodiment of the present invention, preferably, A1, A2, and A4 are all CH, and A3 is CH or N.
Z represents a hydrogen atom or a halogen atom.
The halogen atom represented by Z is, for example, a fluorine atom, a chlorine atom, a bromine atom, or an iodine atom, preferably a fluorine atom or a chlorine atom, and more preferably a fluorine atom.
When Z is a halogen atom, the binding site may be any of A1, A2, A3, and A4, and is, for example A4.
In a preferable embodiment of the present invention, Z is preferably a hydrogen atom.
The compound of formula (II) is a compound that is the less-polar of two diastereomers in which the carbon atom represented by * in formula (II) is an asymmetric carbon atom.
The two diastereomers in which the carbon atom represented by * in formula (II) is an asymmetric carbon atom are, namely, a diastereomer (diastereomer a) in which the configuration of R2 is configuration a:
and a diastereomer (diastereomer b) in which the configuration of R2 is configuration b:
Diastereomer a and diastereomer b each include diastereomer p (the configuration of R6 is configuration p) and diastereomer q (the configuration of R6 is configuration q), in both of which another carbon atom in formula (II) is an asymmetric carbon atom. A diastereomer in which the configuration of R2 is configuration a and the configuration of R6 is configuration p is referred to as “diastereomer ap,” and others are referred to in the same manner. Thus, diastereomer a includes diastereomer ap and diastereomer aq, and diastereomer b includes diastereomer bp and diastereomer bq. The phrase “compound that is the less-polar of two diastereomers” means a compound that is the less-polar of the two diastereomers when the configuration of R6 is fixed (i.e., the configuration of R6 is fixed in configuration p or configuration q), specifically, a compound that is the less-polar of diastereomer ap and diastereomer bp, or a compound that is the less-polar of diastereomer aq and diastereomer bq.
In a preferable embodiment of the present invention, the compound of formula (II) is preferably a compound (diastereomer ap or diastereomer bp; or diastereomer aq or diastereomer bq) that is first eluted when an isomer mixture containing two diastereomers (two diastereomers consisting of diastereomer ap and diastereomer bp, or two diastereomers consisting of diastereomer aq and diastereomer bq) in which the carbon atom indicated by * in formula (II) is an asymmetric carbon atom and in which the configuration of R6 is fixed is subjected to column separation (column type: CHIRAL ART Cellulose-SC, and elution solvent: 40/60/0.1 mixed solvent of n-hexane/ethanol/trifluoroacetic acid), particularly from the viewpoint of the compound being less cytotoxic. More specifically, the column separation is performed under the conditions of flow rate: 2.35 mL/min, temperature: ambient, detection wavelength: UV at 293 nm, injection volume: 18 mg (13 mg/mL), and system: Prominence (Shimadzu).
In an embodiment of the present invention, of the scope of formula (I), formula (IA)
In an embodiment of the present invention, of the scope of formula (II), formula (IIA)
In a preferable embodiment of the present invention, it is preferred that
The salt of the compound can be any pharmaceutically acceptable salt. The salt can be either acidic or basic salts. Examples of acidic salts include inorganic acid salts, such as hydrochloride, hydrobromide, sulfate, nitrate, and phosphate; organic acid salts, such as acetate, propionate, tartarate, fumarate, maleate, malate, citrate, methanesulfonate, and paratoluenesulfonate. Examples of basic salts include alkali metal salts, such as sodium salts and potassium salts; alkaline earth metal salts, such as calcium salts and magnesium salts; salts with ammonia; and salts with organic amines, such as morpholine, piperidine, pyrrolidine, monoalkylamine, dialkylamine, trialkylamine, mono(hydroxyalkyl)amine, di(hydroxyalkyl)amine, and tri(hydroxyalkyl)amine.
The solvate of the compound is not particularly limited. The solvent that constitutes the solvate is, for example, water, or a pharmaceutically acceptable organic solvent (e.g., ethanol, glycerol, and acetic acid).
The compound of the present invention can be produced by various methods.
The compound of the present invention can be produced, for example, by the method described by the following scheme 1 or a method according to this method.
In step a, synthetic intermediate 2 is reacted with synthetic intermediate 3 in the presence of a catalyst and a base to produce synthetic intermediate 4. For example, 1 to 5 equivalents, preferably 1.2 to 3 equivalents, of synthetic intermediate 3 can be used per synthetic intermediate 2. For example, 0.05 to 0.5 equivalents, preferably 0.05 to 0.2 equivalents, of a catalyst can be used per synthetic intermediate 2. For example, 1.5 to 5 equivalents, preferably 1.5 to 3 equivalents, of a base can be used per synthetic intermediate 2. The catalyst is, for example, a rhodium complex, and preferably [RhCl(cod)]2. The base is, for example, N,N-dicyclohexylmethylamine, triethylamine, pyridine, or N,N-diisopropylethylamine; and preferably triethylamine. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, 1,4-dioxane, 1,2-dimethoxyethane, or tetrahydrofuran, and preferably 1,4-dioxane. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 18 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 150° C., and preferably 25° C. to 100° C.
In step b, synthetic intermediate 4 is reacted with iodomethane in the presence of a base to produce synthetic intermediate 5. For example, 1 to 2 equivalents, preferably 1 to 1.8 equivalents, of lithium diisopropylamide can be used per synthetic intermediate 4; and, for example, 1 to 20 equivalents, preferably 1 to 15 equivalents, of iodomethane can be used per synthetic intermediate 4. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 5 hours. The reaction temperature depends on the reagent or solvent for use, but is typically −78° C. to 40° C., and preferably −78° C. to 25° C.
In step c, deprotection of the acetal of synthetic intermediate 5 is performed. An excess amount of hydrochloric acid is used for synthetic intermediate 5. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, methanol, dichloromethane, tetrahydrofuran, or 1,4-dioxane, and preferably methanol or tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 18 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 25° C. to 100° C.
In step d, hydrolysis of synthetic intermediate 4 or its equivalent ester is performed to produce the compound of the present invention. For example, 5 to 20 equivalents, preferably 10 to 20 equivalents, of a base can be used per synthetic intermediate 4. The base is, for example, lithium hydroxide, sodium hydroxide, or potassium hydroxide, and preferably sodium hydroxide or lithium hydroxide. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, methanol, dichloromethane, or tetrahydrofuran, and preferably methanol or tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 18 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 25° C. to 140° C.
The compound of the present invention can also be produced, for example, by the method described by the following scheme 2 or a method according to this method.
Step d of scheme 2 is performed according to scheme 1.
In step e, synthetic intermediate 8 is produced from synthetic intermediate 6 and synthetic intermediate 7. For example, 1 to 1.5 equivalents, preferably 1 to 1.2 equivalents, of synthetic intermediate 7 can be used per synthetic intermediate 6; and, for example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents, of n-butyllithium, can be used per synthetic intermediate 6. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 10 hours, and preferably 1 hour to 4 hours. The reaction temperature depends on the reagent or solvent for use, but is typically −80° C. to 25° C., and preferably −78° C. to 25° C.
In step f, synthetic intermediate 9 is produced from synthetic intermediate 8. For example, 1 to 3 equivalents, preferably 1 to 2 equivalents, of trichloroacetonitrile can be used per synthetic intermediate 8. For example, 0.01 to 0.1 equivalents, preferably 0.01 to 0.05 equivalents, of 1,8-diazabicyclo[5,4,0]-7-undecene can be used per synthetic intermediate 8. For example, 1 to 3 equivalents, preferably 1 to 2.5 equivalents, of dimethylketene methyl trimethylsilyl acetal can be used per synthetic intermediate 8. For example, 0.01 to 0.1 equivalents, preferably 0.05 to 0.1 equivalents, of bis(trifluoromethanesulfonyl)imide can be used per synthetic intermediate 8. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, tetrahydrofuran, or acetonitrile, and preferably acetonitrile. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 10 hours, and preferably 1 hour to 5 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 25° C., and preferably 10° C. to 25° C.
In step g, synthetic intermediate 10 is produced from synthetic intermediate 9. For example, 1 to 3 equivalents, preferably 1 to 2.5 equivalents, of 2,3-dichloro-5,6-dicyano-p-benzoquinone can be used per synthetic intermediate 9. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, a mixed solvent of dichloromethane and water. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 5 hours, and preferably 1 hour to 3 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 25° C., and preferably 10° C. to 25° C.
In step h, synthetic intermediate 12 is produced from synthetic intermediate 10 and synthetic intermediate 11. For example, 1 to 2 equivalents, preferably 1 to 1.2 equivalents, of synthetic intermediate 11 can be used per synthetic intermediate 10. For example, 1 to 2 equivalents, preferably 1 to 1.2 equivalents, of triphenylphosphine can be used per synthetic intermediate 10. For example, 1 to 1.5 equivalents, preferably 1 to 1.2 equivalents, of diethyl azodicarboxylate can be used per synthetic intermediate 10. Instead of diethyl azodicarboxylate, for example, bis(2-methoxyethyl)azodicarboxylate, diisopropyl azodicarboxylate, or cyanomethylenetributylphosphorane can be used. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, 1,4-dioxane, tetrahydrofuran, toluene, or N,N-dimethylformamide, and preferably tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 5 hours to 8 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 40° C., and preferably 0° C. to 25° C.
Synthetic intermediate 2, synthetic intermediate 6, and synthetic intermediate 11 in schemes 1 and 2 can be produced by a known method, such as the method disclosed in PTL 1 (WO2015/092713), the method disclosed in WO2016/202253, or a method according the methods. For example, these synthetic intermediates can be produced in accordance with the following scheme 3.
Step h in scheme 3 is performed according to scheme 2.
In step i, amination of synthetic intermediate 13 is performed to produce synthetic intermediate 14. An excess amount of ammonia water is used for synthetic intermediate 13. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 18 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 25° C. to 40° C.
In step j, synthetic intermediate 14 is reacted with synthetic intermediate 15 to produce synthetic intermediate 11 via synthetic intermediate 16.
In the first step, synthetic intermediate 14 and synthetic intermediate 15 are reacted in the presence of a base. For example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents of a base can be used per synthetic intermediate 14. For example, 0.8 to 1.5 equivalents, preferably 0.8 to 1.2 equivalents, of synthetic intermediate 15 can be used per synthetic intermediate 14. The base is, for example, potassium carbonate, or sodium carbonate, preferably potassium carbonate. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, a mixed solvent of an organic solvent (e.g., tetrahydrofuran or dimethylformamide) and water, and preferably a mixed solvent of tetrahydrofuran and water. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 3 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 25° C. to 40° C.
In the second step, synthetic intermediate 11 is produced from synthetic intermediate 16 in the presence of a base. For example, 1 to 5 equivalents, preferably 2 to 3 equivalents, of a base can be used per synthetic intermediate 16. The base is, for example, potassium tert-butoxide, potassium carbonate, or potassium hydroxide, and preferably potassium tert-butoxide. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dimethyl sulfoxide, or dimethylformamide, and preferably dimethyl sulfoxide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 3 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 60° C. to 100° C.
In step k, a reduction reaction of synthetic intermediate 17 is performed to produce synthetic intermediate 18. For example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents, of a reducing agent can be used per synthetic intermediate 17. The reducing agent is, for example, a borane-tetrahydrofuran complex or a borane-dimethylsulfide complex. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 40 hours, and preferably 1 hour to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 25° C. to 150° C., and preferably 25° C. to 40° C.
In step 1, synthetic intermediate 19 is reacted with bispinacolato diboron in the presence of a base and a catalyst to produce synthetic intermediate 2. For example, 1 to 3 equivalents, preferably 1 to 2.5 equivalents, of a base can be used per synthetic intermediate 19. For example, 0.05 to 0.1 equivalents, preferably 0.05 to 0.08 equivalents, of a catalyst can be used per synthetic intermediate 19. For example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents, of bispinacolato diboron can be used per synthetic intermediate 19. The base for use is, for example, potassium acetate. The catalyst is, for example, a palladium catalyst such as PdCl2(dppf)2·CH2Cl2 or Pd2(dba)3, and preferably PdCl2(dppf)2·CH2Cl2. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, 1,4-dioxane, tetrahydrofuran, dimethyl sulfoxide, or N,N-dimethylformamide, and preferably 1,4-dioxane. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 5 hours to 8 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 60° C. to 120° C., and preferably 60° C. to 100° C.
In step m, synthetic intermediate 20 is produced from synthetic intermediate 18. For example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents, of sodium hydride can be used per synthetic intermediate 20. For example, 1 to 2 equivalents, preferably 1 to 1.2 equivalents, of p-methoxybenzyl chloride can be used per synthetic intermediate 20. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran, or N,N-dimethylformamide, and preferably N,N-dimethylformamide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 5 hours to 15 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 60° C., and preferably 0° C. to 25° C.
In step n, synthetic intermediate 6 is produced from synthetic intermediate 20. For example, 1 to 1.5 equivalents, preferably 1 to 1.2 equivalents, of n-butyllithium can be used per synthetic intermediate 20. For example, 1 to 2 equivalents, preferably 1 to 1.5 equivalents, of N,N-dimethylformamide can be used per synthetic intermediate 20. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 10 hours, and preferably 1 hour to 3 hours. The reaction temperature depends on the reagent or solvent for use, but is typically −80° C. to 25° C., and preferably −78° C. to 25° C.
Synthetic intermediate 3 can be obtained, for example, by the methods described in the following schemes 4 to 7 or a method according to these methods.
In step o, synthetic intermediate 21 is reacted with N,O-dimethylhydroxylamine hydrochloride in the presence of a base, a condensing agent, and an additive to produce synthetic intermediate 22. Typically, 1 to 3 equivalents, preferably 1.5 to 2 equivalents of N,O-dimethylhydroxylamine hydrochloride can be used per synthetic intermediate 21. Typically, 1 to 3 equivalents, preferably 1 to 2 equivalents, of a condensing agent can be used per synthetic intermediate 21. Typically, 0.1 to 2 equivalents, preferably 1 to 2 equivalents, of an additive can be used per synthetic intermediate 21. Typically, 0.5 to 5 equivalents, preferably 2 to 4 equivalents, of a base can be used per synthetic intermediate 21. The condensing agent is, for example, N,N′-dicyclohexylcarbodiimide, 1,1-carbonyldiimidazole, 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride, benzotriazol-1-yl oxytripyrrolidinophosphonium hexafluorophosphate, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate, O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate, diethyl cyanophosphate, diphenylphosphoryl azide, trifluoroacetic acid pentafluorophenyl ester, or isopropylchloroformate, preferably 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride, or O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate. The additive is, for example, 1-hydroxybenzotriazole, 1-hydroxy-7-azabenzotriazole, or N-hydroxysuccinimide, and preferably 1-hydroxybenzotriazole. The base is, for example, triethylamine, pyridine, N,N-diisopropylethylamine, or 4-dimethylaminopyridine, and preferably triethylamine, N,N-diisopropylethylamine, or 4-dimethylaminopyridine. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, diethyl ether, acetonitrile, or N,N-dimethylformamide, and is preferably dichloromethane or N,N-dimethylformamide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 25° C. to 40° C.
In step p, synthetic intermediate 23 or synthetic intermediate 25 is produced from synthetic intermediate 22 or synthetic intermediate 24 by bromination. Typically, 1 to 5 equivalents, preferably 2 to 3 equivalents, of N-bromosuccinimide can be used per synthetic intermediate 22 or synthetic intermediate 24. Typically, 1 to 3 equivalents, preferably 1 to 2 equivalents, of trifluoroacetic acid can be used per synthetic intermediate 22 or synthetic intermediate 24. Instead of trifluoroacetic acid, for example, concentrated sulfuric acid, concentrated hydrochloric acid, or acetic acid can be used. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, carbon tetrachloride, 1,2-dimethoxyethane, or N,N-dimethylformamide, and preferably N,N-dimethylformamide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 25° C. to 40° C.
In step q, synthetic intermediate 25 is produced from synthetic intermediate 23. For example, 1 to 3 equivalents, preferably 1 to 1.5 equivalents, of methyl magnesium bromide can be used per synthetic intermediate 23. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, or diethyl ether, and preferably tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 0° C. to 40° C.
In step r, synthetic intermediate 25 is reacted with ethylene glycol in the presence of an acid catalyst to produce synthetic intermediate 26. For example, 0.1 to 5 equivalents, preferably 0.1 to 0.5 equivalents, of an acid catalyst can be used per synthetic intermediate 25. For example, 5 to 20 equivalents, preferably 10 to 15 equivalents, of ethylene glycol can be used per synthetic intermediate 25. The acid catalyst is, for example, p-toluenesulfonic acid monohydrate, hydrochloric acid, or trifluoroacetic acid, and preferably p-toluenesulfonic acid monohydrate. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, toluene, or benzene, and is preferably toluene. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 40° C. to 150° C., and preferably 100° C. to 130° C.
In step s, synthetic intermediate 25 or synthetic intermediate 26 is reacted with methyl acrylate in the presence of a catalyst, a base, and an additive to produce synthetic intermediate 27. For example, 0.05 to 0.2 equivalents, preferably 0.05 to 0.1 equivalents, of a catalyst can be used per synthetic intermediate 25 or synthetic intermediate 26. For example, 1.5 to equivalents, preferably 1.5 to 3 equivalents, of a base can be used per synthetic intermediate 25 or synthetic intermediate 26. For example, 0.05 to 0.2 equivalents, preferably 0.05 to 0.1 equivalents, of an additive can be used per synthetic intermediate 25 or synthetic intermediate 26. For example, 1.5 to 3 equivalents, preferably 1.5 to 2 equivalents, of methyl acrylate can be used per synthetic intermediate 25 or synthetic intermediate 26. The catalyst is, for example, a palladium catalyst such as PdCl2(dppf)2·CHCl3, Pd(OAc)2, or PdCl2(PPh3)2, Pd(PPh3)4, and preferably PdCl2(dppf)2·CHCl3. The base is, for example, N,N-dicyclohexylmethylamine, triethylamine, pyridine, or N,N-diisopropylethylamine, and preferably N,N-dicyclohexylmethylamine. The additive is, for example, tetrabutyl ammonium chloride, or tetrabutyl ammonium iodide, and preferably tetrabutyl ammonium chloride. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dimethylformamide, or dimethylacetamide, and preferably dimethylacetamide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 1 hour to 8 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 40° C. to 150° C., and preferably 100° C. to 140° C. with a microwave.
Scheme 5 is performed according to steps o and s of scheme 4. In step o, instead of N,O-dimethylhydroxylamine hydrochloride, a corresponding amine is used.
Step s of scheme 6 is performed according to scheme 4.
In step t, synthetic intermediate 29 is produced from synthetic intermediate 28. For example, 1 to 3 equivalents, preferably 1 to 1.5 equivalents, of methyl magnesium bromide can be used per synthetic intermediate 28. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, or diethyl ether, and preferably tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 0° C. to 40° C.
In step u, oxidation of synthetic intermediate 29 is performed by using a sulfur trioxide-pyridine complex in the presence of a base to produce synthetic intermediate 30. For example, 1 to 5 equivalents, preferably 1 to 3 equivalents, of a base can be used per synthetic intermediate 29. For example, 1 to 3 equivalents, preferably 1 to 2.5 equivalents, of a sulfur trioxide-pyridine complex can be used per synthetic intermediate 29. The base is, for example, triethylamine, pyridine, N,N-diisopropylethylamine, or 4-dimethylaminopyridine, and preferably triethylamine. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is preferably dimethyl sulfoxide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 0° C. to 40° C.
Synthetic intermediate 3 can be produced by a known method, such as the method disclosed in JP2008/273924, or a method according this method. For example, synthetic intermediate 3 can be produced in accordance with the following scheme 7.
Steps p and s of scheme 7 are performed according to scheme 4.
In step v, synthetic intermediate 31 is reacted with tert-butyl amine and acetic acid to produce synthetic intermediate 32. For example, 1 to 3 equivalents, preferably 1 to 1.5 equivalents, of tert-butyl amine can be used per synthetic intermediate 31. For example, 1 to 20 equivalents, preferably 2.5 to 5 equivalents, of acetic acid can be used per synthetic intermediate 31. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, or toluene, and preferably dichloromethane. The reaction time depends on the reagent or solvent for use, but is typically 1 to 5 hours, and preferably 2 to 4 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 40° C., and preferably 10 to 30° C.
In step w, deprotection of tert-butyl amine in synthetic intermediate 33 is performed to produce synthetic intermediate 34. A mixed solvent of trifluoroacetic acid and water is preferably used for synthetic intermediate 33. The ratio of trifluoroacetic acid to water of the mixed solvent (trifluoroacetic acid/water) is 10 to 20/1 to 5, and preferably to 12/1 to 2. The reaction time depends on the reagent or solvent for use, but is typically 1 to 5 hours, and preferably 2 to 4 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 150° C., and preferably 90° C. to 110° C.
The compound of the present invention can also be produced by using synthetic intermediate 38 instead of synthetic intermediate 10 in scheme 2. Synthetic intermediate 38 can be produced, for example, by the method described in the following scheme 8 or a method according to this method.
Each step of scheme 8 is performed according to schemes 1 to 3.
The compound of the present invention can also be produced by using synthetic intermediate 47 instead of synthetic intermediate 2 in scheme 1. Synthetic intermediate 47 can be produced, for example, by the method described in the following scheme 9 or a method according to this method.
Step l in scheme 9 is performed according to scheme 3.
In step x, synthetic intermediate 40 is produced from synthetic intermediate 39. For example, 1 to 2 equivalents, preferably 1 to 1.2 equivalents, of bromine can be used per synthetic intermediate 39. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, acetic acid, or trifluoroacetic acid, and preferably acetic acid. The reaction time depends on the reagent or solvent for use, but is typically 0.5 to 3 hours, and preferably 1 to 2 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 40° C., and preferably 0° C. to 25° C.
In step y, synthetic intermediate 41 is produced from synthetic intermediate 40. For example, 1 to 10 equivalents, preferably 2 to 5 equivalents, of tin(II) chloride can be used per synthetic intermediate 40. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, methanol, ethanol, propanol, or isopropanol, and preferably methanol. The reaction time depends on the reagent or solvent for use, but is typically 1 to 6 hours, and preferably 1.5 to 4 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 60° C. to 80° C.
In step z, synthetic intermediate 42 is produced from synthetic intermediate 41. An excess amount of formic acid is used for synthetic intermediate 41. The reaction time is typically 0.5 to 5 hours, and preferably 1 to 2 hours. The reaction temperature is typically 25° C. to 150° C., and preferably 90° C. to 110° C.
in step a-1, synthetic intermediate 43 is produced from synthetic intermediate 42. For example, 1 to 3 equivalents, preferably 1.1 to 1.3 equivalents, of trityl chloride can be used per synthetic intermediate 42. For example, 1 to 3 equivalents, preferably 1.1 to 1.7 equivalents, of a base can be used per synthetic intermediate 42. The base is, for example, triethylamine, N,N-diisopropylethylamine, pyridine, 4-dimethylaminopyridine, or N-methyl morpholine, and preferably N-methyl morpholine or triethylamine. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, diethyl ether, acetonitrile, or N,N-dimethylformamide, and preferably dichloromethane. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 12 hours, and preferably 1 to 2 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 40° C. to 60° C.
In step a-2, synthetic intermediate 44 is produced from synthetic intermediate 43. For example, 1 to 5 equivalents, preferably 1.5 to 3 equivalents, of a reducing agent can be used per synthetic intermediate 43. The reducing agent is, for example, lithium borohydride, lithium aluminum hydride, lithium borohydride, or a borane-tetrahydrofuran complex, and preferably lithium borohydride. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran, diethyl ether, or 1,2-dimethoxyethane, and preferably tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 0.2 to 3 hours, and preferably 0.5 to 1.5 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 60° C., and preferably 0° C. to 30° C.
In step a-3, synthetic intermediate 45 is produced from synthetic intermediate 44 by reacting methanesulfonyl chloride and lithium chloride in the presence of a base. For example, 1 to equivalents, preferably 1.5 to 2.5 equivalents, of methanesulfonyl chloride can be used per synthetic intermediate 44. For example, 1 to 10 equivalents, preferably 3 to 5 equivalents, of lithium chloride can be used per synthetic intermediate 44. For example, 1 to 10 equivalents, preferably 3 to 8 equivalents, of a base can be used per synthetic intermediate 44. The base is, for example, triethylamine, N,N-diisopropylethylamine, pyridine, 4-dimethylaminopyridine, or N-methyl morpholine, and preferably N,N-diisopropylethylamine. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, or N,N-dimethylformamide, preferably dichloromethane. The reaction time depends on the reagent or solvent for use, but is typically 1 to 24 hours, and preferably 1 to 12 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 40° C., and preferably 0° C. to 25° C.
In step a-4, synthetic intermediate 45 is reacted with synthetic intermediate 11 and tetrabutyl ammonium iodide in the presence of a base to produce synthetic intermediate 46. For example, 1 to 3 equivalents, preferably 1 to 1.2 equivalents, of synthetic intermediate 11 can be used per synthetic intermediate 45. For example, 0.1 to 1 equivalents, preferably 0.1 to 0.2 equivalents, of tetrabutyl ammonium iodide can be used per synthetic intermediate 45. For example, 1 to 5 equivalents, preferably 1 to 3 equivalents, of a base can be used per synthetic intermediate 45. The base is, for example, potassium carbonate, sodium carbonate, or sodium hydrogen carbonate, and preferably potassium carbonate. The reaction is typically performed in a solvent. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, tetrahydrofuran, 1,4-dioxane, N,N-dimethylformamide, or N,N-dimethylacetamide, and preferably N,N-dimethylformamide. The reaction time depends on the reagent or solvent for use, but is typically 1 to 24 hours, and preferably 1 to 18 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 60° C., and preferably 25° C. to 40° C.
The compound of the present invention can also be produced, for example, by the method described in the following scheme 10 or a method according to this method.
Steps a-3 and a-4 of scheme 10 are performed according to scheme 9, and step d is performed according to scheme 1.
The compound of the present invention can also be produced, for example, by the method described in the following scheme 11 or a method according to this method.
Steps c and d of scheme 11 are performed according to scheme 1. Step g is performed according to scheme 2, and steps a-3 and a-4 are performed according to scheme 9.
In step a-5, compound 49 is produced from compound 9. Per compound 9, 2 to 5 equivalents, preferably 2 to 3 equivalents, of tetrabutyl ammonium fluoride are used. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, tetrahydrofuran, or N,N-dimethylformamide, and preferably tetrahydrofuran. The reaction time depends on the reagent or solvent for use, but is typically 1 to 24 hours, and preferably 1 to 3 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 25° C. to 40° C.
In step a-6, compound 50 is produced from compound 49. Per compound 49, 10 to 50 equivalents, preferably 25 to 50 equivalents, of manganese dioxide are used. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, acetone, benzene, toluene, tetrahydrofuran, or 1,4-dioxane, and preferably dichloromethane. The reaction time depends on the reagent or solvent for use, but is typically 1 to 24 hours, and preferably 2 to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 25° C. to 40° C.
In step a-7, compound 52 is produced from compound 51. Per compound 51, 1 to 5 equivalents, preferably 3 to 5 equivalents, of TMS ethanol are used. Typically 1 to 3 equivalents, preferably 1.5 to 2 equivalents, of a condensing agent are used. Typically 1 to 5 equivalents, preferably 2 to 5 equivalents, of a base are used. The condensing agent is, for example, N,N′-dicyclohexylcarbodiimide, 1,1′-carbonyldiimidazole, 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride, benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate, O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate, diethylcyanophosphate, diphenylphosphoryl azide, trifluoroacetic acid pentafluorophenyl ester, or isopropylchloroformate, and preferably O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate or O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate. The base is, for example, triethylamine, pyridine, N,N-diisopropylethylamine, or 4-dimethylaminopyridine, and preferably triethylamine, N,N-diisopropylethylamine, or 4-dimethylaminopyridine. The solvent can be any solvent that does not adversely affect the reaction, and is, for example, dichloromethane, chloroform, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, diethyl ether, acetonitrile, or N,N-dimethylformamide, and preferably dichloromethane or N,N-dimethylformamide. The reaction time depends on the reagent or solvent for use, but is typically 1 hour to 24 hours, and preferably 3 hours to 24 hours. The reaction temperature depends on the reagent or solvent for use, but is typically 0° C. to 100° C., and preferably 25° C. to 40° C.
The compound of formula (I) can be obtained, for example, by performing separation into a syn-isomer mixture in which the configuration of R1 and the configuration of R2 are syn (S,S and R,R) and an anti-isomer mixture in which the configuration of R1 and the configuration of R2 are anti (S,R and R,S)(separation 1) at any stage of each scheme described above, performing the subsequent synthesis reaction described in the scheme using the anti-isomer mixture, and separating the compound of formula (I) from the anti-isomer mixture (separation 2) in the final stage. Separation 1 can be performed, for example, by silica gel column chromatography. In separation 1, the anti-isomer mixture has, for example, a longer retention time than the syn-isomer mixture. Separation 2 can be performed, for example, by chromatography using a chiral column. The configuration of the resulting separated product can be identified by analyzing the separated product as described later in Test Example 2.
The compound of formula (II) can be separated and identified as described in section “1-8. Polarity.”
The produced compound of the present invention can be isolated or purified as an educt, or as a salt thereof by performing an ordinary salt-forming treatment. The method for isolation or purification is not particularly limited. For example, a commonly used method, such as crystallization, recrystallization, distillation, liquid separation, or chromatography can be suitably selected. Isolation or purification can also be performed by a combination of these methods. When multiple isomers are present, purification can yield a single isomer or a mixture of multiple isomers. When purification yields a single type of isomers or multiple isomer mixtures, these isomers or isomer mixtures can be used as the compound of the present invention as they are, or in combination. The solvate can be obtained by a known method. The structure of the product can be identified, for example, by elemental analysis, MS (ESI-MS) analysis, IR analysis, 1H-NMR, or 13C-NMR.
The compound of the present invention has Nrf2-activating action. Thus, the compound of the present invention (in the present specification, “the active ingredient of the present invention”) can be used as, for example, a medicament or a reagent. From this viewpoint, in its one embodiment, the present invention relates to a medicament containing the active ingredient of the present invention (in the present specification, “the medicament of the present invention”).
The medicament of the present invention can be used as, for example, an Nrf2 activator, or an oxidative-stress defense gene expression activator, based on the action of the active ingredient of the present invention.
The medicament of the present invention can be used in the prevention or treatment of various diseases. The target disease can be any disease that can be prevented or treated based on the above-described action of the active ingredient of the present invention. The medicament of the present invention can be used in the prevention or treatment of diseases or symptoms in which Nrf2 participates or that are associated with the regulation of Nrf2 activity. The medicament of the present invention can be administered to a patient in need of activation of Nrf2, for example, a patient with a disease in which Nrf2 participates. The term “treatment” refers to preventing the aggravation of a disability or disease, slowing its progress, and maintaining, reducing, or eliminating its condition when the disability or disease develops. The term “prevention” refers to preventing the onset of a disability or disease before it develops. Examples of target ophthalmic diseases include dry eyes, diabetic retinopathy, retinitis pigmentosa, glaucoma, cataracts, age-related macular degeneration, proliferative vitreoretinopathy, retinal artery occlusion, retinal vein occlusion, uveitis, Leber's hereditary optic neuropathy, retinopathy of prematurity, retinal detachment, retinal pigment epithelial detachment, optic neuropathy caused by these diseases, optic neuropathy caused by glaucoma, ischemic optic neuropathy, inflammation suppression after surgery, and pain suppression. Examples of target skin diseases include UV-induced skin damage, UV-induced epidermal blistering, psoriasis, atopic dermatitis, and scleroderma. Examples of target otologic diseases include noise-induced hearing loss, and sensorineural hearing loss. Examples of target brain diseases include Alzheimer's disease, Parkinson's disease, Huntington's disease, Batten disease, dementia, and epilepsy. Examples of target lung diseases include asthma, pulmonary and bronchial infection, and chronic obstructive lung disease. Examples of target kidney diseases include diabetic nephropathy, Alport syndrome, autosomal dominant polycystic kidney disease, focal segmental glomerulosclerosis, and IgA nephropathy. Examples of other target diseases include arteriosclerosis, hypertension, cancer, cardiac arrest, Friedreich's ataxia, amyotrophic lateral sclerosis, hepatitis, rheumatoid arthritis, pancreatitis, vasculitis, esophagitis, ulcerative colitis, neutropenia, cell-mediated immunity, diabetes, mitochondrial myopathy, sickle cell anemia, and multiple sclerosis. Of these, multiple sclerosis, psoriasis, Alzheimer's disease, and ophthalmic diseases such as retinitis pigmentosa, glaucoma, and cataracts are preferable.
The target of administration of the medicament of the present invention is not particularly limited, and is, for example, a mammal (e.g., humans, mice, rats, hamsters, rabbits, cats, dogs, cows, sheep, and monkeys).
The administration route of the medicament of the present invention is not particularly limited. For example, the following administration route can be used: peroral administration, tube feeding, and enteral administration such as enema administration; parenteral administration such as intravenous administration, transarterial administration, intramuscular administration, intracardiac administration, subcutaneous administration, intradermal administration, and intraperitoneal administration; ocular topical administration (e.g., eye drop administration, intravitreal administration, subconjunctival administration, and Sub-Tenon administration); and local administration such as dermal administration, inhalation administration, enema administration, ear drop, intranasal administration, and intravaginal administration. Of these, local administration and parenteral administration are preferable. The medicament of the present invention is preferably in a dosage form suitable for these preferable administration routes. From this viewpoint, the medicament of the present invention is preferably a topically administered formulation or a parenterally administered formulation. In an embodiment, the medicament of the present invention may be an orally administered formulation. In an embodiment, the medicament of the present invention may be, for example, an ophthalmic formulation, an otological formulation, a respiratory formulation, or a dermatological formulation. In the present specification, “X formulation” refers to a formulation applied to diseases treated in the diagnosis and treatment department related to X field in medical facilities. In an embodiment, the medicament of the present invention may be an intravenously administered formulation, an intranasally administered formulation, or a transdermally administered formulation.
The medicament of the present invention can be in a dosage form suitable for the administration route. Examples of dosage forms include eye drops, eye ointments, eye washes, injectable drugs, patches, lotions, creams, powders, granules, tablets, capsules, syrups, fluid medicines, ointments, gels, liniments, suppositories, atomizers, inhalants, sprays, and nasal drops. The medicament in these dosage forms can be prepared by a typical technique widely used in the art. In addition to these formulations, the active ingredient of the present invention can also be made into a formulation of drug delivery system (DDS) such as intraocular implant formulations and microspheres.
The medicament of the present invention may be formed only of the active ingredient of the present invention, or may be a composition optionally containing pharmaceutically acceptable additives (in the present specification, simply “additives”). The medicament of the present invention can be produced by a method known in the technical field of pharmaceutical formulations by mixing the active ingredient of the present invention typically with at least one additive. The additive can be suitably selected according to the dosage form of the formulation preferable for administration. The content of the active ingredient of the present invention in the medicament varies according to the dosage form, dose, etc., and can be suitably selected. For example, the content of the active ingredient of the present invention can be typically 0.01 to 99.9 mass %, and preferably 0.1 to 80 mass % of the entire medicament.
Examples of additives include base materials, carriers, solvents, dispersants, emulsifiers, buffers, stabilizers, excipients, binders, disintegrants, lubricants, thickeners, humectants, colorants, flavors, and chelating agents. These can be suitably selected according to the administration route, dosage form etc.
For example, when an otological formulation containing the active ingredient of the present invention is prepared, the following may be added: water (e.g., purified or sterile water, and injectable distilled water), physiological saline, dextrose solutions, water-soluble organic solvents (lower aliphatic alcohols such as ethanol and isopropanol, and polyalkylene glycols such as ethylene glycol, diethylene glycol, and polyethylene glycol), animal and vegetable oils (vegetable oils such as jojoba oil, olive oil, coconut oil, and cottonseed oil, and animal oils such as squalane), mineral oils (e.g., liquid paraffin, and silicone oil), wax (e.g., beeswax, carnauba wax, lanolin, paraffin, and petrolatum), long-chain fatty acid esters (saturated or unsaturated fatty acid alkyl esters, and esters of fatty acids and polyhydric alcohols (e.g., poly C2-4 alkylene glycol, glycerin or polyglycerin)), hydrogenated oil, higher alcohols (e.g., saturated aliphatic alcohols such as stearyl alcohol, and unsaturated aliphatic alcohols such as oleyl alcohol), and higher fatty acids (e.g., stearic acid, and oleic acid). Additionally, such a formulation may further contain the following: antiseptics or preservatives (e.g., parabens such as methylparaben, and butylparaben), odor-masking agents or fragrances (e.g., deodorizers such as menthol), fresheners, soothing agents (local anesthetics such as lidocaine), and active ingredients for treating infection or inflammation (e.g., antimicrobial agents, antibiotics, anti-inflammatory agents). The amount of these additives varies according to the type and use of the additives for use, and the additives can be added at a concentration that can achieve the purpose of the additives.
For example, when a dermatological formulation containing the active ingredient of the present invention is prepared, a solvent such as purified water, ethanol, isopropanol, or dipropylene glycol can be used singly or in a combination of two or more. The base material includes animal and vegetable fat and oil such as olive oil, soybean oil, camellia oil, sesame oil, peanut oil, cocoa butter, beef tallow, and lard; wax such as carnauba wax, and beeswax; aliphatic alcohols such as octyldodecanol, cetanol, and stearyl alcohol; fatty acids such as oleic acid, palmitic acid, and stearic acid; fat-and-oil base materials such as hydrocarbons (e.g., squalane, white petrolatum, liquid paraffin, ceresin, and microcrystalline wax), and hydrophilic base materials such as gelatin, and macrogol. These can be used singly, or in a combination of two or more. Other additives such as the following can also be added: excipients such as light anhydrous silicic acid, crystalline cellulose, and dextrin; solubilization agents such as diisopropyl adipate, capric acid, crotamiton, and propylene carbonate; suspension agents such as propylene glycol alginate, sodium dioctyl sulfosuccinate, soybean lecithin, and povidone; surfactants or emulsifiers such as polyoxyethylene hydrogenated castor oil, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan monooleate, glycerin monostearate, and sucrose fatty acid ester; viscous agents such as carboxyvinyl polymers, xanthan gum, carboxymethyl cellulose, hydroxypropyl cellulose, and polyvinyl alcohols (partially saponified products); plasticizers such as triacetin, and isopropyl myristate; humectants such as glycerin, 1,3-butylene glycol, sodium DL-pyrrolidone carboxylate, and sodium hyaluronate; stabilizers such as sodium edetate, sorbitol, thymol, and polyoxyethylene polyoxypropylene glycol; antioxidants such as ascorbic acid, sodium erythorbate, tocopheryl acetate, and dibutyl hydroxytoluene; preservatives such as sorbic acid, sodium dehydroacetate, methyl parahydroxybenzoate, ethyl parahydroxybenzoate, and butyl parahydroxybenzoate; and pH adjusters such as hydrochloric acid, citric acid, sodium citrate, acetic acid, sodium acetate, sodium hydroxide, and sodium hydrogenphosphate. The amount of these additives varies according to the type and use of the additives for use, and the additives can be added at a concentration that can achieve the purpose of the additives.
For example, when an ophthalmic formulation containing the active ingredient of the present invention (agents topically applied to the eyes: eye drops, eye ointments, eye washes etc.) is prepared, the following additives may be added: stabilizers (e.g., sodium hydrogen sulfite, sodium thiosulfate, sodium edetate, sodium citrate, ascorbic acid, and dibutylhydroxytoluene), solubilization agents (e.g., glycerin, propylene glycol, macrogol, and polyoxyethylene hydrogenated castor oil), suspension agents (e.g., polyvinyl pyrrolidone, hydroxypropyl methylcellulose, hydroxymethyl cellulose, and sodium carboxymethylcellulose), emulsifiers (e.g., polyvinyl pyrrolidone, soybean lecithin, egg yolk lecithin, polyoxyethylene hydrogenated castor oil, and polysorbate 80), buffers (e.g., phosphate buffer, acetate buffer, borate buffer, carbonate buffer, citrate buffer, Tris buffer, glutamic acid, and epsilon aminocaproic acid), viscous agents (e.g., water-soluble cellulose derivatives such as methylcellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, and carboxymethylcellulose, sodium chondroitin sulfate, sodium hyaluronate, carboxyvinyl polymers, polyvinyl alcohols, polyvinylpyrrolidone, and macrogol), preservatives (e.g., benzalkonium chloride, benzethonium chloride, chlorhexidine gluconate, chlorobutanol, benzyl alcohol, sodium dehydroacetate, parahydroxybenzoic acid esters, sodium edetate, and boric acid), tonicity agents (e.g., sodium chloride, potassium chloride, glycerin, mannitol, sorbitol, boric acid, glucose, and propylene glycol), pH adjusters (e.g., hydrochloric acid, sodium hydroxide, phosphoric acid, acetic acid, boric acid, and citric acid), fresheners (e.g., 1-menthol, d-camphor, d-borneol, and mentha oil), ointment base materials (white petrolatum, refined lanolin, liquid paraffin, and vegetable oil (olive oil, camellia oil, and peanut oil)). The amount of these additives varies according to the type and use of the additives for use, and the additives can be added at a concentration that can achieve the purpose of the additives.
When the medicament of the present invention is formed into an otological composition such as ear drops or nasal drops, the composition can be produced in accordance with a method typically used in the field of pharmaceutical formulations. For example, the composition can be produced in accordance with the method described in the Japanese Pharmacopoeia, 17th Edition (General Rules for Preparations, Preparations for Otic Application, or Preparations for Nasal Application).
When the medicament of the present invention is formed into a dermatological composition, such as an external skin drug, such a composition can be produced in accordance with a method typically used in the field of pharmaceutical formulations. For example, the composition can be produced in accordance with the method described in the Japanese Pharmacopoeia, 17th Edition (General Rules for Preparations, Preparations for Cutaneous Application). When the medicament of the present invention is formed into an ophthalmic composition such as an eye drop or eye ointment, such a composition can be produced in accordance with a method typically used in the field of pharmaceutical formulations. For example, the composition can be produced in accordance with the method described in the Japanese Pharmacopoeia, 17th Edition (General Rules for Preparations, Preparations for Ophthalmic Application (e.g., Ophthalmic Liquids and Solutions, and Ophthalmic Ointments)).
The dose of the medicament of the present invention varies according to the target disease and cannot be generalized. However, the dose can be set such that the concentration of the active ingredient of the present invention in a target tissue where the efficacy is to be exerted is, for example, 0.001 nM to 100 μM, and preferably 0.01 nM to 100 μM.
When the medicament of the present invention is topically used on an eye of an adult, a medicament containing, for example, 0.01 nM to 1000 μM, preferably 0.1 nM to 1000 μM, of the active ingredient of the present invention is preferably applied 1 to 8 times daily, preferably 1 to 5 times daily. An appropriate dose can be suitably determined according to the concentration and dosage form of the active ingredient of the present invention.
The medicament of the present invention may also contain any other one medicinal ingredient, or two or more medicinal ingredients, as long as the effects of the present invention are not impaired.
The present invention is described in more detail below with reference to Reference Examples, Production Examples, Examples, and Test Examples; however, the present invention is not limited thereto.
In the Reference Examples, Production Examples, Examples, and Test Examples, all temperatures were specified in degrees Celsius (° C.) unless otherwise specified. All amounts and percentages are by weight unless otherwise specified. Reagents were purchased from reagent suppliers, such as Sigma-Aldrich Corporation, Tokyo Chemical Industry Co., Ltd., FUJIFIIM Wako Pure Chemical Corporation, and Nacalai Tesque, Inc., and used without purification unless otherwise stated.
The operations in the Reference Examples, Production Examples, and Examples were generally performed under argon atmosphere in an anhydrous solvent. The reaction was analyzed by thin-layer chromatography (TLC), and ended by determination based on the consumption of the starting substance. For TLC, silica gel 60F254 (Merck) was used, samples were developed in appropriate solvents and displayed at appropriate positions, and a UV detector was used for detection. Elution in column chromatography in the Reference Examples, Production Examples, and Examples was carried out under observation by TLC unless otherwise mentioned. The silica gel for column chromatography used was SI silica gel (particle size: 30 to 50 μm) or NH silica gel (particle size: 60 μm) produced by Fuji Silysia Chemical Ltd., or silica gel (particle size: 40 μm) or amino silica gel (particle size: 40 μm) produced by Yamazen Corporation. The term “room temperature” generally means a temperature of about 10° C. to 35° C.
The following abbreviations were used in the Production Examples below.
1H NMR spectra were recorded on a Bruker instrument operating at 400 MHz. NMR spectra were obtained as CDCl3 solutions using chloroform as a reference standard (7.26 ppm) or tetramethylsilane (0.00 ppm) inside as appropriate. Other NMR solvents were also used as needed. When peak multiplicities are reported, the following abbreviations are used: s (singlet), d (doublet), t (triplet), q (quartet), quin (quintet), septd (septet), m (multiplet), br (broad), dd (doublet of doublets), dt (doublet of triplets), and td (triplet of doublets). Coupling constants (J values) are reported in Hertz (Hz).
While stirring ammonia water (about 28%)(84 mL), (R)-(+)-butylene oxide (5.0 mL, 58.2 mmol) was added dropwise over 10 minutes, and the mixture was stirred at room temperature for 22 hours. The solvent of the mixture was distilled under reduced pressure, and the obtained oily substance was dissolved in THF/H2O (72 mL/18 mL). Potassium carbonate (4.55 g, 32.9 mmol) and 2-fluorobenzenesulfonyl chloride (4.3 mL, 32.9 mmol) were added to the solution, and the mixture was stirred at room temperature for 2 hours. The obtained solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was dissolved in DMSO (130 mL), and potassium tert-butoxide (11 g, 98 mmol) was added and stirred at 80° C. for 1 hour. The obtained solution was adjusted to a pH of up to 5 with 2N hydrochloric acid, and then extracted with ethyl acetate. The organic layer was washed with water and then dried over anhydrous sodium sulfate, and the solvent was distilled under reduced pressure. Dichloromethane at 0° C. was added to the obtained residue, followed by filtration. The residue was dried under reduced pressure, thereby obtaining the title compound (3.36 g, 45%) as a white solid. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=3/2→1/1), thereby obtaining the title compound (2.93 g, 39%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.83 (1H, dd, J=7.6, 1.6 Hz), 7.47 (1H, td, J=7.6, 1.6 Hz), 7.19 (1H, td, J=7.6, 1.2 Hz), 7.17 (1H, dd, J=7.6, 1.2 Hz), 4.66 (1H, br s), 3.89-3.82 (1H, m), 3.70-3.62 (1H, m), 3.39 (1H, ddd, J=14.8, 5.2, 2.0 Hz), 1.83-1.71 (1H, m), 1.67-1.56 (1H, m), 1.13 (3H, t, J=7.2 Hz).
(R)-(−)-1-amino-2-propanol (2.89 g, 38.3 mmol), THF/water (125 mL/31.3 mL), potassium carbonate (5.29 g, 38.3 mmol), 2-fluorobenzenesulfonyl chloride (5.0 mL, 38.3 mmol), DMSO (120 mL), and potassium tert-butoxide (10.0 g, 89.1 mmol) were used as raw materials, and the same operation was performed as in step j of Reference Example 1, thereby obtaining the title compound (6.42 g, 79%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.81 (1H, dd, J=8.0, 1.6 Hz), 7.46 (1H, td, J=8.0, 1.6 Hz), 7.19 (1H, td, J=8.0, 1.2 Hz), 7.15 (1H, dd, J=8.0, 1.2 Hz), 4.75 (1H, br s), 4.19-4.12 (1H, m), 3.67-3.59 (1H, m), 3.41 (1H, ddd, J=14.8, 5.2, 2.0 Hz), 1.40 (3H, d, J=6.4 Hz).
Ammonia water (about 28%)(2.9 mL), (R)-(+)-butylene oxide (172 μL, 2 mmol), THF/water (2.4 mL/0.6 mL), potassium carbonate (163.1 mg, 1.18 mmol), 2-chloro-pyridine-3-sulfonyl chloride (250 mg, 1.18 mmol), DMSO (4.7 mL), and potassium tert-butoxide (397 mg, 3.54 mmol) were used as raw materials, and the same operation was performed as in Reference Example 1, thereby obtaining the title compound (210.4 mg, 78%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 8.40 (1H, dd, J=4.8, 2.0 Hz), 8.15 (UH, dd, J=7.6, 2.0 Hz), 7.19 (1H, dd, J=7.6, 4.8 Hz), 6.34 (1H, br s), 4.26-4.21 (1H, m), 3.66-3.58 (1H, m), 3.50-3.44 (1H, m), 1.84-1.75 (1H, m), 1.71-1.65 (1H, m), 1.12 (3H, t, J=7.6 Hz).
Ammonia water (about 28%)(4.35 mL), (R)-(+)-butylene oxide (258 μL, 3 mmol), THF/water (2.5 mL/1.0 mL), potassium carbonate (180 mg, 1.3 mmol), 4-chloro-pyridine-3-sulfonyl chloride (250 mg, 1.18 mmol), DMSO (8.0 mL), and potassium tert-butoxide (397 mg, 3.54 mmol) were used as raw materials, and the same operation was performed as in Reference Example 1, thereby obtaining the title compound (140.8 mg, 52%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 8.82 (1H, s), 8.53 (1H, d, J=5.6 Hz), 7.04 (1H, d, J=5.6, Hz), 5.98 (1H, br s), 4.29-4.23 (1H, m), 3.56-3.46 (2H, m), 1.81-1.74 (1H, m), 1.72-1.63 (1H, m), 1.10 (3H, t, J=7.6 Hz).
Potassium carbonate (203.0 mg, 1.5 mmol) and 2.6-difluorobenzenesulfonyl chloride (150 μL, 1.1 mmol) were added to a THF/water (4/1) (2.0 mL) solution of (R)-1-aminobutan-2-ol (127.6 mg, 1.4 mmol), and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction solution, followed by extraction with ethyl acetate and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (318.1 mg, quant.) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.51 (1H, m), 7.04 (2H, t, J=8.4 Hz), 3.73-3.67 (1H, m), 3.28 (1H, dd, J=12.8, 3.2 Hz), 2.96 (1H, d, J=12.8, 8.0 Hz), 1.55-1.41 (2H, m), 0.94 (3H, t, J=7.6 Hz).
A DMSO (1.5 mL) solution of (R)-2-fluoro-N-(2-hydroxybutyl)benzenesulfonamide (161.0 mg, 0.65 mmol) and potassium tert-butoxide (150.7 mg, 1.3 mmol) was stirred under microwave irradiation at 100° C. for 2 hours. The reaction solution was returned to room temperature, adjusted to a pH of 6 with 1M hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=73/27→52/48), thereby obtaining the title compound (113.2 mg, 71%) as a white solid.
1H NMR (400 MHz, CDCl3) δ7.38-7.33 (1H, m), 6.93-6.88 (2H, m), 5.26 (1H, br t, J=6.0 Hz), 4.34-4.27 (1H, m), 3.54 (1H, ddd, J=14.0, 6.4, 4.0 Hz), 3.23 (1H, ddd, J=14.0, 11.2, 6.8 Hz), 1.78-1.58 (2H, m), 1.07 (3H, t, J=7.6 Hz).
3-Buten-1-ol (2.5 mL, 29.5 mmol) at 0° C. was added to a THF (25 mL) solution of sodium hydride (60%)(2.36 g, 59 mmol), and the mixture was returned to room temperature and stirred for 30 minutes. Benzyl bromide (3.85 mL, 32.4 mmol) was added at 0° C. to the solution, and the mixture was stirred at room temperature for 20 hours. A saturated ammonium chloride aqueous solution was added to the mixture at 0° C. to stop the reaction, followed by extraction with ethyl acetate. The combined organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v) 100/0→91/9), thereby obtaining the title compound (3.95 g, 83%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.38-7.26 (5H, m), 5.91-5.79 (1H, m), 5.15-5.07 (1H, m), 5.08-5.02 (1H, m), 4.53 (2H, s), 3.54 (2H, t, J=6.8 Hz), 2.43-2.35 (2H, m).
mCPBA (about 77%)(7.09 g, 31.6 mmol) was added at 0° C. to a dichloromethane (79 mL) solution of [(but-3-en-1-yloxy)methyl]benzene (3.95 g, 24.3 mmol). The mixture was returned to room temperature and stirred for 14 hours. The reaction mixture was diluted with water, and a saturated sodium hydrogen carbonate aqueous solution and a saturated sodium thiosulfate aqueous solution were added to stop the reaction. The mixture was extracted with dichloromethane, and the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=93/7→72/28), thereby obtaining the title compound (4.11 g, 95%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.38-7.26 (5H, m), 4.54 (2H, s), 3.68-3.58 (2H, m), 3.12-3.06 (1H, m), 2.79 (1H, dd, J=5.0, 4.2 Hz), 2.54 (1H, dd, J=5.0, 3.7 Hz), 1.97-1.86 (1H, m), 1.84-1.73 (1H, m).
2-[2-(Benzyloxy)ethyl]oxirane (4.11 g, 23.1 mmol) was added to ammonia water (about 28%)(86 mL). The reaction mixture was stirred for 15 hours, and then concentrated under reduced pressure, thereby obtaining the title compound (4.45 g, 99%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.37-7.26 (5H, m), 4.52 (2H, s), 3.77-3.63 (3H, m), 2.79 (1H, dd, J=12.8, 3.6 Hz), 2.61 (1H, dd, J=12.8, 7.6 Hz), 1.77-1.71 (2H, m).
Potassium carbonate (2.06 g, 14.9 mmol) and 2-fluorobenzenesulfonyl chloride (1.95 mL, 14.9 mmol) were added to a solution of 1-amino-4-(benzyloxy)butan-2-ol (4.4475 g, 22.8 mmol) in THF (29 mL) and water (7.3 mL). The reaction mixture was stirred for 1 hour, and 1N hydrochloric acid was added to stop the reaction. The mixture was extracted with ethyl acetate, and the organic layer was concentrated under reduced pressure. The obtained residue was dissolved in DMSO (135 mL), and potassium tert-butoxide (5.02 g, 44.7 mmol) was added to the solution. The reaction mixture was stirred at 80° C. for 1 hour, and 1N hydrochloric acid was added to stop the reaction. The mixture was extracted with ethyl acetate, washed with saturated saline, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=91/9→60/40), thereby obtaining the title compound (3.88 g, 78%) as a colorless solid.
1H NMR (400 MHz, CDCl3) δ 7.83 (1H, d, J=7.6 Hz), 7.42 (1H, td, J=7.6, 1.6 Hz), 7.33-7.26 (5H, m), 7.20 (1H, t, J=7.6 Hz), 6.96 (1H, d, J=7.6 Hz), 4.63 (1H, br s), 4.55 (1H, d, J=12.0 Hz), 4.49 (1H, d, J=12.0 Hz), 4.11 (1H, br t, J=9.6 Hz), 3.85-3.63 (3H, m), 3.39-3.35 (1H, m), 2.00-1.86 (2H, m).
After a borane-tetrahydrofuran complex (about 0.9 mmol/L THF solution) (38.8 mL, 34.9 mmol) was added dropwise to a THF (50 mL) solution of 5-bromo-2-methylbenzoate (5.0 g, 25.3 mmol) at 0° C. over 10 minutes, the mixture was stirred at room temperature for 20 hours. Methanol (35 mL) was added to the obtained solution, and the mixture was stirred at room temperature for 2 hours. Then, the solvent was distilled under reduced pressure. Ethyl acetate was added to the residue, followed by washing with 1N hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (5.0 g, 98%) as an oily light yellow substance. 1H NMR (400 MHz, CDCl3) δ 7.53 (1H, d, J=2.0 Hz), 7.32 (1H, dd, J=8.0, 2.0 Hz), 7.03 (1H, d, J=8.0 Hz), 4.66 (2H, d, J=5.6 Hz), 2.27 (3H, s), 1.64 (1H, t, J=5.6 Hz).
A 2.2M DEAD toluene solution (5.1 mL, 11.2 mmol) was added at 0° C. while stirring to a THF (39 mL) solution of (5-bromo-2-methylphenyl)methanol (2.0 g, 9.95 mmol), (R)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (2.26 g, 9.95 mmol), and triphenylphosphine (2.61 g, 9.95 mmol). The solution was stirred at room temperature for 7 hours, and then diluted with water, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→85/15), thereby obtaining the title compound (3.46 g, 85%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, td, J=7.6, 1.6 Hz), 7.39 (1H, d, J=2.0 Hz), 7.35 (1H, dd, J=8.0, 2.0 Hz), 7.26 (1H, td, J=7.6, 1.2 Hz), 7.21 (1H, dd, J=7.6, 1.2 Hz), 7.06 (1H, d, J=8.0 Hz), 4.51 (1H, d, J=14.4 Hz), 4.08-4.02 (1H, m), 3.85 (1H, d, J=14.4 Hz), 3.76 (1H, dd, J=15.2, 10.8 Hz), 3.06 (1H, dd, J=15.2, 2.0 Hz), 2.29 (3H, s), 1.79-1.70 (1H, m), 1.56-1.50 (1H, m), 1.11 (3H, t, J=7.2 Hz).
A 1,4-dioxane solution (36 mL) of (R)-2-(5-bromo-2-methylbenzyl)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (3.4 g, 8.29 mmol), bis(pinacolato)diboron (3.15 g, 12.4 mmol), potassium acetate (2.44 g, 24.9 mmol), and PdCl2(dppf)2-CH2Cl2 (408 mg, 0.5 mmol) was stirred at 100° C. for 6 hours. The reaction solution was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→85/15), thereby obtaining the title compound (3.28 g, 86%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.90 (1H, d, J=7.6 Hz), 7.68 (1H, d, J=7.6 Hz), 7.54 (1H, s), 7.52 (1H, t, J=7.6 Hz), 7.25 (1H, t, J=7.6 Hz), 7.22-7.20 (2H, m), 4.64 (1H, d, J=13.6 Hz), 4.09-4.04 (1H, m), 3.83 (1H, d, J=13.6 Hz), 3.74 (1H, dd, J=15.2, 10.8 Hz), 2.97 (1H, dd, J=15.2, 1.2 Hz), 2.43 (3H, s), 1.77-1.70 (1H, m), 1.51-1.42 (1H, m), 1.32 (12H, s), 1.05 (3H, t, J=7.2 Hz).
Sodium hydride (472 mg, 11.8 mmol) was added to a DMF (16 mL) solution of (5-bromo-2-methylphenyl)methanol (2.16 g, 10.8 mmol). The solution was stirred at room temperature for 30 minutes and then cooled to 0° C., and 4-methoxybenzyl chloride (1.53 mL, 11.3 mmol) was added. The solution was stirred at room temperature for 2 hours, and water was added to stop the reaction, followed by extraction with diethyl ether. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→85/15), thereby obtaining the title compound (1.77 g, 61%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.50 (1H, d, J=2.0 Hz), 7.32-7.28 (3H, m), 7.02 (1H, d, J=8.0 Hz), 6.90 (2H, d, J=8.4 Hz), 4.51 (2H, s), 4.46 (2H, s), 3.81 (3H, s), 2.24 (3H, s).
A 2.3M n-butyllithium hexane solution (980 μL, 2.25 mmol) was added dropwise at −78° C. under argon atmosphere to a THF (6 mL) solution of 4-bromo-2-{[(4-methoxybenzyl)oxy]methyl}-1-methylbenzene (600 mg, 1.87 mmol). The reaction mixture was stirred at −78° C. for 1 hour, DMF (290 μL, 3.75 mmol) was added, and the mixture was heated to room temperature and mixed for 1 hour. A saturated ammonium chloride aqueous solution was added to the mixture to end the reaction, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated saline, and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=99/1→90/10), thereby obtaining the title compound (448.3 mg, 89%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 9.97 (1H, s), 7.87 (1H, d, J=1.6 Hz), 7.72 (1H, dd, J=8.0, 1.6 Hz), 7.33-7.26 (3H, m), 6.90 (2H, br d, J=8.8 Hz), 4.56 (2H, s), 4.54 (2H, s), 3.82 (3H, s), 2.39 (3H, s).
A 1,4-dioxane solution (68 mL) of 4-bromo-2-{[(4-methoxybenzyl)oxy]methyl}-1-methylbenzene (6.67 g, 20.77 mmol), bis(pinacolato)diboron (5.54 g, 21.81 mmol), potassium acetate (6.12 g, 62.31 mmol), and PdCl2(dppf)2-CH2Cl2 (848.1 mg, 1.04 mmol) was stirred at 100° C. for 6 hours. The reaction solution was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→85/15), thereby obtaining the title compound (6.63 g, 87%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.73 (1H, s), 7.65 (1H, dd, J=7.2, 1.2 Hz), 7.27 (2H, d, J=8.8 Hz), 7.18 (1H, d, J=7.2 Hz), 6.88 (2H, br d, J=8.8 Hz), 4.52 (2H, s), 4.47 (2H, s), 3.81 (3H, s), 2.36 (3H, s), 1.34 (12H, s).
Triethylamine (2.7 mL, 19.5 mmol) was added to a 1,4-dioxane/water (9.6 mL/960 μL) solution of methyl (E)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]acrylate (3.30 g, 13.0 mmol), 2-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.39 g, 6.49 mmol), and [RhCl(cod)]2 (160 mg, 0.32 mmol). The reaction mixture was stirred at 50° C. for 2.5 hours. Water was added to the mixture, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→7/3), thereby obtaining the title compound (1.52 g, 47%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.28-7.24 (3H, m), 7.11-7.10 (2H, m), 6.88 (2H, br d, J=8.4 Hz), 6.81 (1H, d, J=3.6 Hz), 6.65 (1H, dd, J=3.6, 0.8 Hz), 4.67 (1H, t, J=7.6 Hz), 4.48 (2H, s), 4.46 (2H, s), 4.00-3.95 (2H, m), 3.94-3.89 (2H, m), 3.81 (3H, s), 3.59 (3H, s), 3.08 (1H, dd, J=15.6, 7.6 Hz), 2.99 (1H, dd, J=15.6, 7.6 Hz), 2.28 (3H, s), 1.71 (3H, s).
A 2M LDA THF/heptane/ethylbenzene solution (1.83 mL, 3.67 mmol) was added under argon atmosphere at −78° C. to a THF (18 mL) solution of methyl 3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (1.40 g, 2.82 mmol). The reaction mixture was stirred at −78° C. for 30 minutes, and then stirred at −40° C. for 20 minutes. Iodomethane (2.6 mL, 42.3 mmol) was added, and the mixture was heated to room temperature and stirred for 4 hours. Water was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=8%), thereby obtaining the title compound. The title compound could be separated into two isomer mixtures; isomer mixture 1 with a shorter retention time (505.7 mg, 31%) and isomer mixture 2 with a longer retention time (853.3 mg, 52%) were obtained as oily light yellow substances. Isomer mixture 2 was used for the next reaction.
Isomer mixture 1: 1H NMR (400 MHz, CDCl3) δ 7.28-7.26 (3H, m), 7.17-7.15 (1H, m), 7.06 (1H, d, J=8.0 Hz), 6.89 (2H, br d, J=8.8 Hz), 6.82 (1H, d, J=3.6 Hz), 6.74 (1H, d, J=3.6 Hz), 4.47 (2H, s), 4.43 (2H, s), 4.25 (1H, d, J=10.8 Hz), 4.01-3.97 (2H, m), 3.96-3.90 (2H, m), 3.81 (3H, s), 3.43 (3H, s), 3.24-3.16 (1H, m), 2.25 (3H, s), 1.71 (3H, s), 1.20 (3H, d, J=6.8 Hz).
Isomer mixture 2: 1H NMR (400 MHz, CDCl3) δ 7.28-7.23 (3H, m), 7.11-7.10 (2H, m), 6.89 (2H, br d, J=8.8 Hz), 6.77 (1H, d, J=3.6 Hz), 6.71 (1H, br d, J=3.6 Hz), 4.48 (2H, s), 4.47 (2H, s), 4.27 (1H, d, J=11.2 Hz), 3.99-3.95 (2H, m), 3.93-3.90 (2H, m), 3.82 (3H, s), 3.58 (3H, s), 3.21-3.16 (1H, m), 2.28 (3H, s), 1.69 (3H, s), 1.05 (3H, d, J=6.8 Hz).
2N hydrochloric acid (1.4 mL) was added to a tetrahydrofuran (2.8 mL) solution of methyl 3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methyl-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (isomer mixture 2) of Reference Example 18 (489 mg, 0.96 mmol), and the mixture was stirred at room temperature for 3 hours. The mixture was neutralized with a 1N sodium hydroxide aqueous solution and extracted with dichloromethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (390.8 mg, 87%) as an oily light yellow substance. 1H NMR (400 MHz, CDCl3) δ 7.46 (1H, d, J=4.0 Hz), 7.29-7.24 (3H, m), 7.11 (2H, s), 6.92-6.89 (3H, m), 4.49 (2H, s), 4.48 (2H, s), 4.36 (1H, d, J=11.2 Hz), 3.82 (3H, s), 3.60 (3H, s), 3.25-3.21 (1H, m), 2.46 (3H, s), 2.26 (3H, s), 1.08 (3H, d, J=6.8 Hz).
DDQ (681 mg, 3.0 mmol) was added at 0° C. to a dichloromethane/water (10/1) (18.2 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{([(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate (700.9 mg, 1.5 mmol). The mixture was stirred at room temperature for 2.5 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=6/4→4/6), thereby obtaining the title compound (436.3 mg, 84%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.46 (1H, d, J=4.0 Hz), 7.28 (1H, br s), 7.13 (2H, br s), 6.93 (1H, d, J=4.0 Hz), 4.68 (2H, d, J=5.6 Hz), 4.37 (1H, d, J=11.2 Hz), 3.60 (3H, s), 3.27-3.23 (1H, m), 2.46 (3H, s), 2.30 (3H, s), 1.09 (3H, d, J=6.8 Hz).
Sodium borohydride (458.2 mg, 12 mmol) was added at 10° C. to a methanol solution (40 mL) of 2-acetyl-5-bromothiophene (1.16 g, 5.6 mmol), and the mixture was stirred at 10° C. for 1 hour and 20 minutes. Water was added to the reaction solution, and the mixture was stirred at 0° C. for 15 minutes. After the reaction solution was concentrated under reduced pressure, ethyl acetate was added, followed by washing with water and saturated saline. After the organic layer was dried over sodium sulfate, the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (1.16 g, 99%) as an oily colorless and transparent substance.
1H NMR (400 MHz, CDCl3) δ 6.90 (1H, d, J=3.6 Hz), 6.72 (1H, d, J=3.6 Hz), 5.04 (1H, dq, J=5.6, 6.4 Hz), 1.97 (1H, d, J=4.8 Hz), 1.57 (3H, d, J=6.4 Hz).
A dichloromethane solution (5.0 mL) of 4-dimethylaminopyridine (76.8 mg, 0.6 mmol), TEA (3.2 mL, 23 mmol), and tert-butyldimethylchlorosilane (1.66 g, 11 mmol) was added at 0° C. to a dichloromethane (12 mL) solution of 1-(5-bromothiophen-2-yl)ethan-1-ol (1.16 g, 5.6 mmol), and the mixture was stirred at room temperature overnight. 4-Dimethylaminopyridine (305.6 mg, 2.5 mmol) and tert-butyldimethylchlorosilane (981.6 mg, 6.5 mmol) were further added to the reaction solution, and the mixture was stirred at room temperature for 3 hours and 45 minutes. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated saline, and the obtained organic layer was dried over sodium sulfate. After the solvent was removed by distillation under reduced pressure, the residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=1/0→95/5), thereby obtaining the title compound (1.28 g, 71%) as an oily colorless and transparent substance.
1H NMR (400 MHz, CDCl3), δ 6.86 (1H, d, J=4.0 Hz), 6.58 (1H, d, J=4.0 Hz), 5.01 (1H, q, J=6.4 Hz), 1.47 (3H, d, J=6.4 Hz), 0.91 (9H, s), 0.09 (3H, s), 0.06 (3H, s).
After an anhydrous THF solution (5.0 mL) of [1-(5-bromothiophen-2-yl)ethoxy](tert-butyl)dimethylsilane (540.9 mg, 1.7 mmol) was cooled to −78° C., 2.5M n-butyllithium (0.75 mL, 1.9 mmol) was added dropwise, and the mixture was stirred at −78° C. for 30 minutes. A THF solution (5 mL) of 3-{[(4-methoxybenzyl)oxy]methyl}-4-methylbenzaldehyde (478.1 mg, 1.8 mmol) was added dropwise to the reaction solution, and the mixture was stirred at −78° C. for 1 hour, and then stirred at room temperature for 30 minutes. The reaction was stopped with a saturated ammonium chloride aqueous solution, followed by extraction with ethyl acetate, and the organic layer was washed with saturated saline. The organic layer was dried over sodium sulfate. After the solvent was removed by distillation under reduced pressure, the obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=90/10→69/31), thereby obtaining the title compound (740.4 mg, 86%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.41 (1H, s), 7.29-7.26 (3H, m), 7.16 (1H, d, J=7.6 Hz), 6.88 (3H, d, J=8.4 Hz), 6.67 (2H, d, J=4.4 Hz), 5.96 (1H, d, J=4.0 Hz), 5.17 (1H, q, J=6.4 Hz), 4.51 (2H, s), 4.48 (2H, s), 3.81 (3H, s), 2.32 (3H, s), 2.29 (1H, d, J=4.0 Hz), 1.47 (3H, d, J=6.4 Hz), 0.90 (9H, s), 0.07 (3H, s), 0.03 (3H, br s).
Trichloroacetonitrile (40 μL, 0.4 mmoL) and DBU (6 μL, 0.1 mmol) were added to an acetonitrile (2.0 mL) solution of ((5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}thiophen-2-yl)(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)methanol (110.7 mg, 0.2 mmol), and the mixture was stirred at room temperature for 30 minutes. Dimethylketene methyl trimethylsilyl acetal (120 μL, 0.6 mmol) and bis(trifluoromethanesulfonyl)imide (8.2 mg, 0.03 mmol) were added to the reaction solution, and the mixture was stirred at room temperature for 1 hour. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction solution to stop the reaction, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v) a 95/5→74/26), thereby obtaining the title compound (824.8 mg, 73%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.32 (1H, dd, J=4.4, 1.2 Hz), 7.29-7.26 (2H, m), 7.21 (1H, td, J=7.6, 1.6 Hz), 7.08 (1H, d, J=7.6 Hz), 6.90 (1H, s), 6.88 (1H, s), 6.76-6.74 (1H, m), 6.64-6.63 (1H, m), 5.00 (1H, q, J=6.4 Hz), 4.63-4.62 (1H, m), 4.49 (2H, s), 4.47 (2H, br s), 3.81 (3H, s), 3.56 (3H, s), 2.27 (3H, s), 1.45 (3H, d, J=6.4 Hz), 1.29 (3H, s), 1.22 (3H, s), 0.89 (9H, br s), 0.05 (3H, s), 0.002 (3H, s).
DDQ (612.2 mg, 2.7 mmol) was added at 0° C. to a mixed solution of methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}thiophen-2-yl)-3-(3-{([(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (773 mg, 1.3 mmol) in dichloromethane (16 mL) and water (1.2 mL), and the mixture was stirred at 0° C. for 1 hour and 20 minutes. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction solution to stop the reaction, followed by extraction with dichloromethane. After the organic layer was dried over sodium sulfate, the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=93/7→72/28→50/50), thereby obtaining the title compound (204.1 mg, 44%) as an oily colorless and transparent substance.
1H NMR (400 MHz, CDCl3) δ 7.50 (1H, d, J=4.0 Hz), 7.34 (1H, d, J=1.6 Hz), 7.20 (1H, dd, J=7.6, 1.6 Hz), 7.11 (1H, d, J=7.6 Hz), 6.97 (1H, d, J=4.0 Hz), 4.17 (1H, s), 4.68 (2H, d, J=5.6 Hz), 3.61 (3H, s), 2.49 (3H, s), 2.31 (3H, s), 1.32 (3H, s), 1.24 (3H, s).
DIPEA (300 μL, 1.7 mmol) and methanesulfonyl chloride (88 μL, 1.1 mmol) were added to a suspension of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (204.1 mg, 0.57 mmol) and lithium chloride (123.1 mg, 2.9 mmol) in dichloromethane (6.0 mL), and the mixture was stirred at room temperature for 4.5 hours. Ethyl acetate was added to the reaction solution, followed by washing with a 10% citric acid aqueous solution, a saturated sodium hydrogen carbonate aqueous solution, and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (218.3 mg, quant.) as an oily transparent light brown substance.
1H NMR (400 MHz, CDCl3) δ 7.51 (1H, d, J=4.0 Hz), 7.31-7.24 (2H, m), 7.14 (1H, d, J=8.0 Hz), 6.87 (1H, d, J=4.0 Hz), 4.70 (1H, s), 4.57 (2H, s), 3.60 (3H, s), 2.50 (3H, s), 2.38 (3H, s), 1.31 (3H, s), 1.24 (3H, s).
A DMF (0.50 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (29.8 mg, 0.079 mmol), (R)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1.1-dioxide (27.8 mg, 0.12 mmol), potassium carbonate (33.9 mg, 0.25 mmol), and tetrabutylammonium iodide (5.7 mg, 0.015 mmol) was stirred at 70° C. for 3 hours and 10 minutes. The reaction solution was cooled to room temperature, and ethyl acetate was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=73/27→52/48), thereby obtaining the title compound (43.1 mg, 96%) as a white solid.
1H NMR (400 Mz, CDCl3) δ 7.87 (1H, dt, J=7.6, 1.2 Hz), 7.55-7.50 (1H, m), 7.49 (1H, d, J=4.0 Hz), 7.27-7.11 (5H, m), 6.97-6.95 (1H, m), 4.69 (1H, br s), 4.56-4.55 (1H, m), 3.83-3.80 (1H, m), 4.04-3.97 (1H, m), 3.73-3.71 (1H, m), 3.60 (3H, br s), 2.96-2.93 (1H, m), 2.49-2.48 (3H, m), 2.33 (3H, s), 1.81-1.56 (1H, m), 1.51-1.35 (1H, m), 1.29 (3H, br s), 1.23-1.21 (3H, m), 1.10-1.08 (3H, m).
An acetic acid solution (5.0 mL) of bromine (5.0 g, 32 mmol) was added to an acetic acid (30 mL) solution of methyl 2-amino-3-nitrobenzoate (5.30 g, 27 mmol), and the mixture was stirred at room temperature for 1 hour. Crushed ice and water were added to the reaction solution, and the mixture was stirred at room temperature for 10 minutes. The resultant was filtered to obtain the precipitated solid, and the solid was washed with water, dissolved in ethyl acetate, washed with a 1M sodium hydroxide aqueous solution and saturated saline, and dried over sodium sulfate. The solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (7.37 g, 99%) as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 8.51 (1H, d, J=2.4 Hz), 8.44 (2H, br s), 8.32 (1H, d, J=2.4 Hz), 3.93 (3H, s).
Tin(II) chloride (13.6 g, 72 mmol) was added to a methanol (100 mL) solution of methyl 2-amino-5-bromo-3-nitrobenzoate (3.97 g, 14 mmol), and the mixture was stirred at 75° C. for 1.5 hours. The reaction solution was returned to room temperature, and the reaction solution was concentrated under reduced pressure. Water was added, and a 1M sodium hydroxide aqueous solution (100 mL) and solid sodium hydrogen carbonate were added to adjust the pH to 9, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=70/30→49/51), thereby obtaining the title compound (2.60 g, 73%) as a brown solid.
1H NMR (400 MHz, CDCl3) δ 7.58 (1H, d, J=1.6 Hz), 6.94 (1H d, J=1.6 Hz), 5.55 (2H, br s), 3.87 (3H, s), 3.39 (2H, br s).
A formic acid (10 mL) solution of methyl 2,3-diamino-5-bromobenzoate (1.02 g, 4.2 mmol) was stirred at 100° C. for 1 hour. The reaction solution was returned to room temperature, and a 1M sodium hydroxide aqueous solution and solid sodium hydrogen carbonate were added to adjust the pH to 9, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (1.06 g, 99%) as a purple solid.
1H NMR (400 MHz, CDCl3) δ 10.5 (1H, br s), 8.18 (1H, d, J=0.8 Hz), 8.14 (1H, s), 8.07 (1H, d, J=0.8 Hz), 4.02 (3H, s).
N-methylmorpholine (550 μL, 5.3 mmol) and trityl chloride (1.17 g, 4.2 mmol) were added to a dichloromethane (16 mL) solution of methyl 6-bromo-1H-benzo[d]imidazole-4-carboxylate (854.6 mg, 3.4 mmol), and the mixture was stirred at 55° C. for 2 hours. The reaction solution was returned to room temperature, and ethyl acetate was added, followed by washing with a saturated sodium carbonate aqueous solution and saturated saline, and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure. The obtained residue was dissolved in THF (12 mL), and a 2M lithium boron hydride THF solution (3.4 mL, 6.8 mmol) was added and stirred at room temperature for 1 hour. Water was added to the reaction solution to stop the reaction, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=72/28→7/93→CH3Cl2/MeOH=100/0→95/5), thereby obtaining the title compound (1.17 g, 74%) as a light purple solid.
1H NMR (400 MHz, CDCl3) δ 7.85 (1H, s), 7.36-7.31 (9H, m), 7.21 (1H, s), 7.17-7.14 (6H, m), 6.50 (1H, s), 5.09 (2H, d, J=6.4 Hz), 3.67 (1H, t, J=6.4 Hz).
DIPEA (0.77 mL, 4.4 mmol) and methanesulfonyl chloride (115 μL, 1.5 mmol) were added to a dichloromethane (2.5 mL) solution of (6-bromo-1-trityl-1H-benzo[d]imidazol-4-yl)methanol (343.7 mg, 0.73 mmol) and lithium chloride (126.3 mg, 3.0 mmol), and the mixture was stirred at 25° C. for 12 hours. The reaction solution was diluted with ethyl acetate, washed with water and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was dissolved in a mixed solvent of DMF (3.0 mL) and dichloromethane (1.0 mL), and (R)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1.1-dioxide (173.9 mg, 0.77 mmol), tetrabutylammonium iodide (55.8 mg, 0.15 mmol), and potassium carbonate (315.6 mg, 2.3 mmol) were added to the reaction solution. The reaction solution was stirred at 40° C. for 5.5 hours, and returned to room temperature. Then, the resultant was diluted with a mixed solvent of ethyl acetate/hexane (1/1), washed with water and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=69/31→48/52), thereby obtaining the title compound (471.8 mg, 95%) as a light orange solid.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.78 (1H, s), 7.49 (1H, td, J=7.6, 1.6 Hz), 7.46 (1H, s), 7.34-7.30 (9H, m), 7.23 (1H, t, J=8.0 Hz), 7.17-7.11 (7H, m), 6.50 (1H, d, J=1.6 Hz), 4.77 (1H, d, J=16.0 Hz), 4.55 (1H, d, J=16.0 Hz), 4.05-3.96 (2H, m), 3.30 (1H, dt, J=13.6, 6.8 Hz), 1.78-1.67 (1H, m), 1.54-1.44 (1H, m), 1.08 (3H, t, J=7.2 Hz).
An anhydrous 1,4-dioxane (2.0 mL) solution of (R)-2-[(6-bromo-1-trityl-1H-benzo[d]imidazol-4-yl)methyl]-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (202.2 mg, 0.30 mmol), bis(pinacolato)diboron (83.0 mg, 0.33 mmol), PdCl2(dppf)2-CH2Cl2 (12.8 mg, 0.016 mmol), and potassium acetate (90.8 mg, 0.93 mmol) was stirred under argon atmosphere at 90° C. for 15.5 hours. The reaction solution was returned to room temperature and filtered through Celite, and the solvent of the obtained filtrate was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=76/24→55/45), thereby obtaining a compound (170.6 mg), about half of which was an unreacted product. An anhydrous 1,4-dioxane (2.0 mL) solution of the obtained compound (0.13 mmol), bis(pinacolato)diboron (83.0 mg, 0.33 mmol), PdCl2(dppf)2-CH2Cl2 (12.8 mg, 0.016 mmol), and potassium acetate (90.8 mg, 0.93 mmol) was stirred again at 90° C. for 15.5 hours. The reaction solution was returned to room temperature and filtered through Celite, and the solvent of the obtained filtrate was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=76/24→55/45), thereby obtaining the title compound (138.9 mg, 64%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.92 (1H, d, J=7.6 Hz), 7.84 (1H, s), 7.71 (1H, s), 7.46 (1H, t, J=7.6 Hz), 7.32-7.28 (9H, m), 7.21 (1H, t, J=7.6 Hz), 7.16-7.14 (7H, m), 6.77 (1H, s), 4.81 (1H, d, J=14.8 Hz), 4.58 (1H, d, J=14.8 Hz), 4.06-3.94 (2H, m), 3.27 (1H, d, J=14.0 Hz), 1.72-1.62 (1H, m), 1.49-1.40 (1H, m), 1.20 (12H, s), 1.03 (3H, t, J=7.2 Hz).
Bromine (5.0 g, 31 mmol) was added at 0° C. to a dichloromethane (25 mL) solution of 3-methylthiophene-2-carboxaldehyde (3.75 g, 30 mmol), and the mixture was stirred at 65° C. for 1 hour. The reaction solution was returned to room temperature, and the reaction solution was diluted with dichloromethane, and washed with a sodium thiosulfate aqueous solution, water, and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. After the obtained residue was purified by silica gel chromatography (hexane/ethyl acetate (v/v)=98/2→90/10), followed by recrystallization with ethyl acetate/hexane, thereby obtaining the title compound (2.06 g, 33%) as a light yellow crystal. Further, after the filtrate was concentrated, hexane was added, and the precipitate was obtained by filtration, thereby obtaining the title compound (1.41 g, 23%) as a light brown solid.
1H NMR (400 MHz, CDCl3) δ 9.90 (1H, s), 6.96 (1H, s), 2.53 (3H, s).
An acetone (3.0 mL) solution of 5-bromo-3-methylthiophene-2-carbaldehyde (317.1 mg, 1.6 mmol) was cooled to 0° C., and 2.5M Jones reagent (3.75 mL, 3.8 mmol)(CrO3:1.01 g, H2SO4: 1.0 mL, H2O: 3.0 mL) was added. The mixture was stirred at 0° C. for 5 minutes, and then stirred at 25° C. for 2 hours and 15 minutes. Water was added to the reaction solution to stop the reaction, ethyl acetate was added to separate the organic layer and the aqueous layer, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (304.2 mg, 89%) as an orange solid.
1H NMR (400 MHz, DMSO-d6) δ 7.20 (1H, s), 2.43 (3H, s).
TEA (439 μL, 3.1 mmol) was added to an acetonitrile (3.3 mL) solution of 5-bromofuran-2-carboxylic acid (500 mg, 2.6 mmol), methylamine hydrochloride (212.3 mg, 3.1 mmol), EDCI (603 mg, 3.1 mmol), and HOBt (106.2 mg, 0.79 mmol). After the reaction mixture was stirred at room temperature for 14 hours, water was added, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=70/30→50/50), thereby obtaining the title compound (391.3 mg, 73%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.04 (1H, d, J=3.6 Hz), 6.62 (1H, s), 6.42 (1H, d, J=3.6 Hz), 2.96 (3H, d, J=4.8 Hz).
5-Bromofuran-2-carboxylic acid (1.0 g, 5.2 mmol), pyrrolidine (517 μL, 6.3 mmol), EDCI (1.2 g, 6.3 mmol), HOBt (212 mg, 1.6 mmol), acetonitrile (6.6 mL), and TEA (878 μL, 6.3 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (748.8 mg, 58%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.04 (1H, d, J=3.6 Hz), 6.43 (1H, d, J=3.6 Hz), 3.82 (2H, t, J=6.8 Hz), 3.63 (2H, t, J=6.8 Hz), 2.01 (2H, quin, J=6.8 Hz), 1.90 (2H, quin, J=6.8 Hz).
5-Bromofuran-2-carboxylic acid (1.0 g, 5.24 mmol), isopropylamine (540 μL, 6.3 mmol), EDCI (1.2 g, 6.3 mmol), HOBt (212 mg, 1.57 mmol), acetonitrile (6.6 mL), and TEA (878 μL, 6.3 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (714.3 mg, 59%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.04 (1H, d, J=3.2 Hz), 6.43 (1H, d, J=3.2 Hz), 6.09 (1H, br s), 4.24 (1H, septd, J=6.4, 1.2 Hz), 1.26 (6H, d, J=6.4 Hz).
5-Bromothiophene-2-carboxylic acid (500 mg, 2.4 mmol), methylamine hydrochloride (325 mg, 4.8 mmol), EDCI (554 mg, 2.9 mmol), HOBt (97.7 mg, 0.72 mmol), acetonitrile (5.0 mL), and TEA (1.0 mL, 7.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (239.8 mg, 45V) as a white solid.
1H NMR (400 MHz, CD3OD) δ 7.40 (1H, d, J=4.0 Hz), 7.13 (1H, d, J=4.0 Hz), 2.86 (3H, s).
5-Bromofuran-2-carboxylic acid (300 mg, 1.6 mmol), 2-methoxyethylamine (340 μL, 5.2 mmol), EDCI (602 mg, 3.1 mmol), HOBt (212 mg, 1.6 mmol), acetonitrile (3.0 mL), and TEA (500 μL, 6.8 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (339.9 mg, 87%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.06 (1H, d, J=3.6 Hz), 6.63 (1H, br s), 6.43 (1H, d, J=3.6 Hz), 3.63-3.59 (2H, m), 3.55-3.53 (2H, m), 3.40 (3H, s).
3-Methylfuran-2-carboxylic acid (720 mg, 5.7 mmol), methylamine hydrochloride (581 mg, 8.6 mmol), EDCI (1.3 g, 6.8 mmol), HOBt (459 mg, 3.4 mmol), acetonitrile (10 mL), and TEA (2.4 mL, 17 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (693.6 mg, 87%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.32 (1H, s), 6.28 (1H, br s), 2.95 (3H, d, J=5.2 Hz), 2.40 (3H, s).
4-Bromothiophene-2-carboxylic acid (1.0 g, 4.83 mmol), methylamine hydrochloride (652 mg, 9.7 mmol), EDCI (1.1 g, 5.8 mmol), HOBt (392 mg, 2.9 mmol), acetonitrile (15 mL), and TEA (2.0 mL, 15 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (789.1 mg, 74%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.37 (1H, d, J=1.2 Hz), 7.35 (1H, d, J=1.2 Hz), 5.93 (1H, br s), 3.00 (3H, d, J=4.8 Hz).
4-Methylthiophene-2-carboxylic acid (1.0 g, 7.0 mmol), methylamine hydrochloride (945.3 mg, 14 mmol), EDCI (1.61 g, 8.4 mmol), HOBt (662 mg, 4.9 mmol), acetonitrile (5.0 mL), dichloromethane (5.0 mL), and TEA (2.94 mL, 21 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (880.5 mg, 81%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.45 (1H, d, J=1.2 Hz), 7.29 (1H, br s), 7.00 (1H, br s), 2.96 (3H, d, J=4.8 Hz), 2.20 (3H, d, J=0.8 Hz).
4-Methylthiophene-2-carboxylic acid (700 mg, 4.9 mmol), N,O-dimethylhydroxylamine hydrochloride (1.44 g, 15 mmol), EDCI (1.88 g, 9.8 mmol), HOBt (1.32 g, 9.8 mmol), dichloromethane (20 mL), and DIPEA (2.6 mL, 15 μmmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (831.5 mg, 91%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.75 (1H, d, J=1.6 Hz), 7.14 (1H, d, J=1.6 Hz), 3.76 (3H, s), 3.36 (3H, s), 2.28 (3H, s).
3-Fluorothiophene-2-carboxylic acid (500 mg, 3.4 mmol), N,O-dimethylhydroxylamine hydrochloride (1.0 g, 10 mmol), EDCI (1.31 g, 6.8 mmol), HOBt (924.3 mg, 6.8 mmol), dichloromethane (20 mL), and DIPEA (1.84 mL, 10 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (604.6 mg, 94%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.38 (1H, dd, J=5.6, 4.0 Hz), 6.84 (1H, d, J=5.6 Hz), 3.74 (3H, s), 3.33 (3H, s).
5-Bromothiophene-2-carboxylic acid (400 mg, 1.9 mmol), 2,4-dimethoxybenzylamine (582 μL, 3.9 mmol), EDCI (1.31 g, 6.8 mmol), HOBt (924.3 mg, 6.8 mmol), dichloromethane (20 mL), and DIPEA (1.84 mL, 10 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (860.9 mg, quant.) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.21 (1H, d, J=8.0 Hz), 7.19 (1H, d, J=4.0 Hz), 6.98 (1H, d, J=4.0 Hz), 6.48 (1H, br s), 6.46 (1H, d, J=2.4 Hz), 6.43 (1H, dd, J=8.0, 2.4 Hz), 4.49 (2H, d, J=5.6 Hz), 3.84 (3H, s), 3.79 (3H, s).
TEA (0.57 mL, 4.1 mmol) was added to a dichloromethane (5.0 mL) solution of 5-bromo-3-methylthiophene-2-carboxylic acid (302.3 mg, 1.4 mmol), N,O-dimethylhydroxylamine hydrochloride (267.4 mg, 2.7 mmol), and EDCI (397.6 mg, 2.1 mmol), and the mixture was stirred at 25° C. for 18 hours. The reaction solution was diluted with ethyl acetate, washed with 1M hydrochloric acid and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (315.3 mg, 87%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 6.87 (1H, s), 3.70 (3H, s), 3.29 (3H, s), 2.51 (3H, s).
TEA (1.5 mL, 11 mmol) was added to a solution of 2-bromothiazole-5-carboxylic acid (707.9 mg, 3.4 mmol), N,O-dimethylhydroxylamine hydrochloride (667.5 mg, 6.8 mmol), and EDCI (977.9 mg, 5.1 mmol) in dichloromethane (17 mL) and IMF (3.0 mL), and the mixture was stirred at 25° C. for 13 hours. Ethyl acetate was added to the reaction solution, followed by washing with 1M hydrochloric acid and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (519.1 mg, 61%) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 8.32 (1H, s), 3.78 (3H, s), 3.36 (3H, s).
TEA (1.0 mL, 7.2 mmol) was added to a solution of 2-bromo-4-methylthiazole-5-carboxylic acid (500.2 mg, 2.3 mmol), N,O-dimethylhydroxylamine hydrochloride (452.8 mg, 4.6 mmol), and EDCI (654.6 mg, 3.4 mmol) in dichloromethane (8.0 mL) and DMF (2.0 mL), and the mixture was stirred at 25° C. for 8 hours. The reaction solution was diluted with ethyl acetate, and washed with 1M hydrochloric acid and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (473.5 mg, 79%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 3.66 (3H, s), 3.26 (3H, s), 2.68 (3H, s).
4-Bromothiophene-2-carboxylic acid (500 mg, 2.4 mmol), N,O-dimethylhydroxylamine hydrochloride (470 mg, 4.8 mmol), EDCI (924 mg, 4.8 mmol), HOBt (708 mg, 5.2 mmol), dichloromethane (20 mL), and DIPEA (1.29 mL, 7.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (510.5 mg, 85%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.83 (1H, d, J=1.6 Hz), 7.44 (1H, d, J=1.6 Hz), 3.78 (3H, s), 3.37 (3H, s).
2-Bromothiophene-3-carboxylic acid (500 mg, 2.4 mmol), N,O-dimethylhydroxylamine hydrochloride (470 mg, 4.8 mmol), EDCI (924 mg, 4.8 mmol), HOBt (326 mg, 4.8 mmol), dichloromethane (20 mL), and DIPEA (1.29 mL, 7.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (606.7 mg, quant.) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) 7.25 (1H, d, J=6.0 Hz), 7.04 (1H, d, J=6.0 Hz), 3.60 (3H, s), 3.34 (3H, s).
5-Bromofuran-2-carboxylic acid (500 mg, 2.6 mmol), N,O-dimethylhydroxylamine hydrochloride (767 mg, 7.9 mmol), EDCI (1.0 g, 5.2 mmol), HOBt (708 mg, 5.2 mmol), dichloromethane (20 mL), and DIPEA (1.4 mL, 7.9 mmol) were used as raw materials, and the same operation was performed as in Reference Example 36, thereby obtaining the title compound (555.3 mg, 90%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.08 (1H, d, J=3.6 Hz), 6.44 (1H, d, J=3.6 Hz), 3.77 (3H, s), 3.33 (3H, s).
Isopropylamine (514 μL, 6.0 mmol) and acetic acid (50 μL, 0.79 mmol) were added to a methanol (7.0 mL) solution of 5-bromofuran-2-carbaldehyde (700 mg, 4.0 mmol), and the mixture was stirred at room temperature for 2 hours. Sodium borohydride (227 mg, 6.0 mmol) was added to the mixture, and stirred at room temperature for 16 hours. The mixture was diluted with a 1N sodium hydroxide aqueous solution, and extracted with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (785.4 mg, 90%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 6.21 (1H, d, J=3.2 Hz), 6.15 (1H, d, J=3.2 Hz), 3.75 (2H, s), 2.82 (1H, septd, J=6.4 Hz), 1.38 (1H, br s), 1.06 (6H, d, J=6.4 Hz).
Tert-butylamine (4.0 mL, 38 mmol) and acetic acid (8.5 mL, 149 mmol) were added at 0° C. to an anhydrous dichloromethane solution (260 mL) of 2,3-thiophenedicarboxaldehyde (4.14 g, 30 mmol), and the mixture was stirred at 0° C. for 15 minutes, and then stirred at room temperature for 3.5 hours. After completion of the reaction, the reaction solution was washed with 1M hydrochloric acid and a saturated sodium hydrogen carbonate aqueous solution, the obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=84/16→63/37), thereby obtaining the title compound (4.03 g, 70%) as a light orange solid.
1H NMR (400 MHz, CDCl3) δ 7.56 (1H, d, J=4.8 Hz), 6.99 (1H, d, J=4.8 Hz), 4.36 (2H, s), 1.54 (9H, s)
N-bromosuccinimide (475.2 mg, 2.7 mmol) was added to a DMF (3.0 mL) solution of 1,5,6,7-tetrahydro-4H-indol-4-one (300 mg, 2.2 mmol), and the mixture was stirred at room temperature for 14 hours. A 4N sodium hydroxide aqueous solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=6/4→5/5), thereby obtaining the title compound (220.5 mg, 76%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 8.49 (1H, br s), 6.51 (1H, d, J=2.4 Hz), 2.79 (2H, t, J=6.4 Hz), 2.48 (2H, t, J=6.4 Hz), 2.15 (2H, quin, J=6.4 Hz).
N,3-dimethylfuran-2-carboxamide (310 mg, 2.2 mmol), DMF (2.3 mL), N-bromosuccinimide (477 mg, 2.7 mmol), and TFA (341 μL, 4.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (205.3 mg, 42%) as an oily yellow substance.
1H NMR (400 MHz, CDCl3) δ 6.28 (1H, br s), 6.27 (1H, s), 2.95 (3H, d, J=4.8 Hz), 2.37 (3H, s).
N,4-dimethylthiophene-2-carboxamide (600 mg, 3.9 mmol), dimethylformamide (6.0 mL), N-bromosuccinimide (822 mg, 4.6 mmol), and TFA (588 μL, 7.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (763.8 mg, 84%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.19 (1H, s), 6.23 (1H, br s), 2.95 (3H, d, J=4.8 Hz), 2.18 (3H, s).
1-(2,4-Dimethyl-1H-pyrrol-3-yl)ethan-1-one (500 mg, 3.6 mmol), DMF (5.0 mL), and N-bromosuccinimide (778 mg, 4.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (538.9 mg, 68%) as a red solid.
1H NMR (400 MHz, CDCl3) δ 8.16 (1H, br s), 2.49 (3H, s), 2.42 (3H, s), 2.22 (3H, s).
1-(4-Methylthiophen-2-yl)ethan-1-one (100 mg, 0.71 mmol), DMF (1.0 mL), N-bromosuccinimide (152.4 mg, 0.86 mmol), and TFA (110 μL, 1.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (118.6 mg, 76%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.36 (1H, s), 2.48 (3H, s), 2.22 (3H, s).
N-bromosuccinimide (1.17 g, 6.6 mmol) and TFA (1.0 mL, 13 mmol) were added to a DMF (6.0 mL) solution of 3-fluoro-N-methoxy-N-methylthiophene-2-carboxamide (620 mg, 3.3 mmol). After the reaction mixture was stirred at room temperature for 24 hours, a 1N sodium hydroxide aqueous solution was added, followed by extraction with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=100/0→80/20), thereby obtaining the title compound (425.5 mg, 48%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.89 (1H, s), 3.75 (3H, s), 3.30 (3H, s).
1-(2,4-Dimethyl-1H-pyrrol-3-yl)ethan-1-one (500 mg, 3.6 mmol), DMF (5.0 mL), and N-bromosuccinimide (778 mg, 4.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (538.9 mg, 68%) as a red solid.
1H NMR (400 MHz, CDCl3) δ 8.16 (1H, br s), 2.49 (3H, s), 2.42 (3H, s), 2.22 (3H, s).
1-(1-Ethyl-1H-pyrrol-2-yl)ethan-1-one (600 μL, 4.3 mmol), DMF (6.0 mL), and N-bromosuccinimide (925 mg, 5.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (752 mg, 80%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.91 (1H, d, J=1.6 Hz), 6.85 (1H, d, J=1.6 Hz), 4.33 (2H, q, J=7.2 Hz), 2.40 (3H, s), 1.35 (3H, t, J=7.2 Hz).
Cyclopropyl(thiophen-2-yl)methanone (593 μL, 4.6 mmol), DMF (5.8 mL), N-bromosuccinimide (979 mg, 5.5 mmol), and TFA (704 μL, 9.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (56.8 mg, 5%) as an oily pale red substance.
1H NMR (400 MHz, CDCl3) δ 7.55 (1H, d, J=4.0 Hz), 7.12 (1H, d, J=4.0 Hz), 2.47-2.41 (1H, m), 1.25-1.21 (2H, m), 1.05-1.01 (2H, m).
N-bromosuccinimide (7.37 g, 41 mmol) and acetic acid (1.3 mL, 23 mmol) were added at 0° C. to a DMF (100 mL) solution of 5-(tert-butyl)-4,5-dihydro-6H-thieno[2,3-c]pyrrol-6-one (4.03 g, 21 mmol), and the mixture was stirred at room temperature for 8 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction solution to stop the reaction, followed by extraction with ethyl acetate/hexane (1/1). The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=96/4→75/25), thereby obtaining the title compound (4.27 g, 76%) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.01 (1H, s), 4.33 (2H, s), 1.53 (9H, s).
1-Methyl-1H-pyrrole-2-carbonitrile (300 mg, 2.8 mmol), DMF (7.0 mL), and N-bromosuccinimide (604.5 mg, 3.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 55, thereby obtaining the title compound (212.5 mg, 41%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 6.81 (1H, d, J=1.6 Hz), 6.75 (1H, d, J=1.6 Hz), 3.76 (3H, s).
A DMSO (4.0 mL) solution of 2-bromo-1,5,6,7-tetrahydro-4H-indol-4-one (200 mg, 0.93 mmol) and potassium tert-butoxide (113.6 mg, 1.0 mmol) was stirred at 60° C. for 30 minutes. Iodomethane (86 μL, 1.4 mmol) was added and stirred at 60° C. for 7 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=7/3→1/1), thereby obtaining the title compound (170.1 mg, 80%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 6.52 (1H, s), 3.50 (3H, s), 2.73 (2H, t, J=6.4 Hz), 2.41 (2H, t, J=6.4 Hz), 2.14 (2H, quin, J=6.4 Hz).
1-(5-Bromo-2,4-dimethyl-1H-pyrrol-3-yl)ethan-1-one (300 mg, 1.4 mmol) was added to a DMF (4.0 mL) solution of sodium hydride (50.4 mg, 1.7 mmol). The mixture was stirred at room temperature for 1 hour, and iodomethane (105 μL, 1.7 mmol) was added and stirred for 20 hours. Further, iodomethane (86 μL, 1.4 mmol) was added and stirred at 60° C. for 7 hours. Water was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=0→9/1), thereby obtaining the title compound (152.8 mg, 48%) as a pale red solid.
1H NMR (400 MHz, CDCl3) δ 3.50 (3H, s), 2.50 (3H, s), 2.41 (3H, s), 2.24 (3H, s).
A methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (0.80 mL, 2.4 mmol) solution was added at 0° C. to a THF (8.0 mL) solution of 5-bromo-3-fluoro-N-methoxy-N-methylthiophene-2-carboxamide (425 mg, 1.6 mmol). After the mixture was stirred at room temperature for 7.5 hours, the reaction was stopped with a saturated ammonium chloride aqueous solution, followed by extraction with diethyl ether. The organic layer was washed with a saturated ammonium chloride aqueous solution and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (190.8 mg, 54%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.90 (1H, d, J=0.8 Hz), 2.52 (3H, d, J=3.2 Hz).
N-methoxy-N,4-dimethylthiophene-2-carboxamide (400 mg, 2.2 mmol), THF (11 mL), and a methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (1.1 mL, 3.2 mmol) solution were used as raw materials, and the same operation was performed as in Reference Example 68, thereby obtaining the title compound (275.1 mg, 91%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.50 (1H, d, J=0.8 Hz), 7.22 (1H, br d, J=0.8 Hz), 2.53 (3H, s), 2.29 (3H, d, J=0.8 Hz).
5-Bromo-N-methoxy-N, 3-dimethylthiophene-2-carboxamide (368 mg, 1.4 mmol), THF (7.0 mL), and a methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (0.70 mL, 2.1 mmol) solution were used as raw materials, and the same operation was performed as in Reference Example 68, thereby obtaining the title compound (216.1 mg, 71%) as an oily yellow substance.
1H NMR (400 MHz, CDCl3) δ 6.93 (1H, s), 2.51 (3H, s), 2.47 (3H, s).
A methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (0.68 mL, 2.0 mmol) solution was added to a THF (7.0 mL) solution of 2-bromo-N-methoxy-N-methylthiazole-5-carboxamide (507.5 mg, 2.0 mmol), and the mixture was stirred at 25° C. for 1 hour. Further, methylmagnesium bromide (3H, 0.15 mL, 0.45 mmol) was added and stirred at room temperature for 5 minutes. A saturated ammonium chloride aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (278 mg, 67%) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 8.05, (1H, s), 2.56 (3H, s).
A methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (0.3 mL, 0.9 mmol) solution was added at 0° C. to a THF (2.0 mL) solution of 2-bromo-N-methoxy-N-4-dimethylthiazole-5-carboxamide (209.0 mg, 0.8 mmol), and the mixture was stirred at room temperature for 10 minutes. A saturated ammonium chloride aqueous solution was added to the reaction solution to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=82/18→61/39), thereby obtaining the title compound (146.8 mg, 85%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 2.72 (3H, s), 2.51 (3H, s).
4-Bromo-N-methoxy-N-methylthiophene-2-carboxamide (510 mg, 2.0 mmol), THF (10 mL), and a methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (1.0 mL, 3.0 mmol) solution were used as raw materials, and the same operation was performed as in Reference Example 68, thereby obtaining the title compound (406.9 mg, 97%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.58 (1H, d, J=1.2 Hz), 7.53 (1H, d, J=1.2 Hz), 2.55 (3H, s).
2-Bromo-N-methoxy-N-methylthiophene-3-carboxamide (550 mg, 2.2 mmol), THF (10 mL), and a methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (1.1 mL, 3.3 mmol) solution were used as raw materials, and the same operation was performed as in Reference Example 68, thereby obtaining the title compound (128.8 mg, 29%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.35 (1H, d, J=5.6 Hz), 7.23 (1H, d, J=5.6 Hz), 2.62 (3H, s).
5-Bromo-N-methoxy-N-methylfuran-2-carboxamide (332.6 mg, 1.4 mmol), THF (7.0 mL), and methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (0.7 mL, 2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 68, thereby obtaining the title compound (223.3 mg, 78%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.12 (1H, d, J=3.6 Hz), 6.49 (1H, d, J=3.6 Hz), 2.46 (3H, s).
Ethylene glycol (0.95 mL, 17 mmol) and p-TsOH-H2O (130 mg, 0.68 mmol) were added to a toluene (34 mL) solution of 1-(5-bromothiophen-2-yl)ethan-1-one (500 mg, 2.4 mmol), and the mixture was stirred under heating and refluxing for 25 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→9/1), thereby obtaining the title compound (183.7 mg, 30%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 6.90 (1H, d, J=4.0 Hz), 6.79 (1H, d, J=4.0 Hz), 4.06-4.00 (m, 2H), 3.99-3.93 (m, 2H), 1.73 (s, 3H).
Ethylene glycol (1.2 mL, 22 mmol) and p-TsOH-H2O (0.11 mmol) were added to a toluene (20 mL) solution of 1-(5-bromo-3-methylthiophen-2-yl)ethan-1-one (491.5 mg, 2.2 mmol), and the mixture was stirred under heating and refluxing for 10 hours. The reaction solution was returned to room temperature, and a saturated sodium hydrogen carbonate aqueous solution was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (577.9 mg, 98%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 6.74 (1H, s), 4.06-3.99 (2H, m), 3.96-3.90 (2H, m), 2.23 (3H, s), 1.71 (3H, s).
Ethylene glycol (800 μL) and p-TsOH-H2O (12.7 mg, 0.067 mmol) were added to a toluene (8.0 mL) solution of 1-(2-bromothiazol-5-yl)ethan-1-one (278 mg, 1.3 mmol), and the mixture was stirred under heating and refluxing for 14 hours. The reaction solution was returned to room temperature, a saturated sodium hydrogen carbonate aqueous solution and ethyl acetate were added to separate the organic layer and the aqueous layer. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (313.6 mg, 93) as an oily yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.49 (1H, s), 4.13-4.03 (2H, m), 3.99-3.91 (2H, m), 1.75 (3H, s).
Ethylene glycol (0.40 mL) and p-TsOH-H2O (6.3 mg, 0.033 mmol) were added to a toluene (8.0 mL) solution of 1-(2-bromo-4-methylthiazol-5-yl)ethan-1-one (146.8 mg, 0.67 mmol), and the mixture was stirred under heating and refluxing for 21 hours. The reaction solution was returned to room temperature, and a saturated sodium hydrogen carbonate aqueous solution was added, followed by extraction with ethyl acetate and washing with saturated saline. The solvent was removed by distillation under reduced pressure. Since the reaction did not proceed completely, toluene (8.0 mL), ethylene glycol (0.80 mL), and p-TsOH-H2O (5.7 mg, 0.030 mmol) were added to the residue, and the mixture was stirred under heating and refluxing for 13 hours. The reaction solution was returned to room temperature, and a saturated sodium hydrogen carbonate aqueous solution was added, followed by extraction with ethyl acetate and washing with saturated saline. The solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (172.2 mg, 98%) as an oily orange substance.
1H NMR (400 MHz, CDCl3) δ 4.09-4.01 (2H, m), 3.94-3.88 (2H, m), 2.43 (3H, s), 1.71 (3H, s).
1-(5-Bromofuran-2-yl)ethan-1-one (533.5 mg, 2.8 mmol), ethylene glycol (1.7 mL, 31 mmol), p-TsOH-H2O (27 mg, 0.14 mmol), and toluene (32 mL) were used as raw materials, and the same operation was performed as in Reference Example 76, thereby obtaining the title compound (496.3 mg, 76%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.29 (1H, d, J=3.2 Hz), 6.23 (1H, d, J=3.2 Hz), 4.07-4.03 (2H, m), 4.01-3.97 (2H, m), 1.71 (3H, s).
1-(5-Bromothiophen-3-yl)ethan-1-one (398 mg, 1.9 mmol), ethylene glycol (1.08 mL, 19. mmol), p-TsOH-H2O (18.5 mg, 0.097 mmol), and toluene (22 mL) were used as raw materials, and the same operation was performed as in Reference Example 76, thereby obtaining the title compound (322.2 mg, 67%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.17 (1H, d, J=1.6 Hz), 7.02 (1H, d, J=1.6 Hz), 4.07-3.98 (2H, m), 3.91-3.82 (2H, m), 1.64 (3H, s).
Methylmagnesium bromide (3H, 2-methyltetrahydrofuran solution) (907 μL, 2.7 mol) was added at 0° C. to a THF (8.0 mL) solution of 5-bromothiophene-3-carbaldehyde (200 μL, 1.8 mmol), and the mixture was stirred at room temperature for 1.5 hours. A saturated ammonium chloride aqueous solution was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with a saturated ammonium chloride aqueous solution and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (503.8 mg, quant.) as a white solid.
1H NMR (400 MHz, CDCl3) δ 6.97 (1H, d, J=0.8 Hz), 6.94 (1H, br s), 4.76 (1H, q, J=6.4 Hz), 2.20 (1H, br s), 1.38 (3H, d, J=6.4 Hz).
TEA (868 μL, 6.2 mmol) and a pyridine-sulfur trioxide complex (832 mg, 5.2 mmol) were added to a DMSO (8.0 mL) solution of 1-(5-bromothiophen-3-yl)ethan-1-ol (503.8 mg, 1.8 mmol), and the mixture was stirred at room temperature for 6 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=95/5→80/20), thereby obtaining the title compound (397.2 mg, quant.) as a white solid.
1H NMR (400 MHz, CDCl3) 7.91 (1H, d, J=1.6 Hz), 7.49 (1H, d, J=1.6 Hz), 2.49 (3H, s).
An anhydrous THF (2.5 mL) solution of 2-bromo-5-(2-methyl-1,3-dioxolan-2-yl)thiazole (215.2 mg, 0.86 mmol) was cooled to −78° C., and n-butyllithium (1.6M hexane solution) (0.6 mL, 0.96 mmol) was added and stirred at −78° C. for 30 minutes. Anhydrous DMF (240 μL, 3.1 mmol) was added to the reaction solution and stirred at −78° C. for 15 minutes. Then, the mixture was heated to −60° C. and further stirred for 50 minutes. A saturated ammonium chloride aqueous solution was added at −60° C. to the reaction solution, followed by extraction with diethyl ether and drying over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography, thereby obtaining the title compound (96.0 mg, 56%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 9.93 (1H, s), 8.01 (1H, s), 4.12-4.06 (2H, m), 3.99-3.93 (2H, m), 1.80 (3H, s).
A solution of 2-bromo-5-(tert-butyl)-4,5-dihydro-6H-thieno[2,3-c]pyrrol-6-one (3.78 g, 14 mmol) in TFA (50 mL) and water (5.0 mL) was stirred at 105° C. for 19 hours. The reaction solution was cooled to room temperature, and the solution was concentrated by distillation under reduced pressure. A saturated sodium hydrogen carbonate aqueous solution was added to the obtained residue, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (3.25 g, quant.) as a brown solid. 1H NMR (400 MHz, CDCl3) δ 7.08 (1H, s), 6.16 (1H, br s), 4.36 (2H, s).
Sodium borohydride (203.5 mg, 5.4 mmol) was added to a methanol (3.6 mL) solution of 1-(5-bromo-3-fluorothiophen-2-yl)ethan-1-one (600.7 mg, 2.7 mmol), and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated under reduced pressure. The reaction was stopped with a 4N sodium hydroxide aqueous solution, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (588.5 mg, 86%) as an oily pale red substance.
1H NMR (400 MHz, CDCl3) δ 6.75 (1H, br s), 5.22-5.17 (1H, m), 2.00 (1H, d, J=4.0 Hz), 1.54 (1H, d, J=6.4 Hz).
A DMF (4.1 mL) solution of tert-butyldimethylsilyl chloride (417.5 mg, 2.8 mmol) was added at 0° C. to a DMP (1.5 mL) solution of 1-(5-bromo-3-fluorothiophen-2-yl)ethan-1-ol (588.5 mg, 2.3 mmol) and imidazole (204.4 mg, 3.0 mmol), and the mixture was stirred at room temperature for 23 hours. The reaction mixture was diluted with water and extracted with diethyl ether. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=1/0→95/5), thereby obtaining the title compound (581 mg, 74%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 6.70 (1H, br s), 5.13 (1H, qd, J=6.4, 1.2 Hz), 1.45 (3H, d, J=6.4 Hz), 0.91 (9H, s), 0.082 (3H, s), 0.036 (3H, s).
Methyl acrylate (215 μL, 2.4 mmol) and N,N-dicyclohexylmethylamine (515 μL, 2.4 mmol) were added to a DMA (1.4 mL) solution of 5-bromo-N-methylfuran-2-carboxamide (163.3 mg, 0.80 mmol), tetrabutylammonium chloride (32.7 mg, 0.04 mmol), and PdCl2(dppf)2-CH2Cl2 (22.2 mg, 0.08 mmol), and the mixture was stirred at 110° C. for 17 hours. The obtained solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=3/2→2/3), thereby obtaining the title compound (103.8 mg, 62%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.41 (1H, d, J=16.0 Hz), 7.13 (1H, d, J=3.6 Hz), 6.67 (1H, d, J=3.6 Hz), 6.52 (1H, br s), 6.41 (1H, d, J=16.0 Hz), 3.80 (3H, s), 3.01 (3H, d, J=4.8 Hz).
(5-Bromofuran-2-yl)(pyrrolidin-1-yl)methanone (583 mg, 2.4 mmol), tetrabutylammonium chloride (66.7 mg, 0.24 mmol), PdCl2(dppf)2-CH2Cl2 (98 mg, 0.12 mmol), DMA (4.8 mL), methyl acrylate (643 μL, 7.2 mmol), and N,N-dicyclohexylmethylamine (761 μL, 3.6 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (478.2 mg, 80%) as a brown solid.
1H NMR (400 MHz, CDCl3) 7.44 (1H, d, J=16.0 Hz), 7.14 (1H, d, J=3.6 Hz), 6.71 (1H, d, J=3.6 Hz), 6.37 (1H, d, J=16.0 Hz), 3.90 (2H, t, J=6.8 Hz), 3.80 (3H, s), 3.65 (2H, t, J=6.8 Hz), 2.05 (2H, quin, J=6.8 Hz), 1.92 (2H, quin, J=6.8 Hz).
5-Bromo-N-isopropylfuran-2-carboxamide (546.2 mg, 2.4 mmol), tetrabutylammonium chloride (65.3 mg, 0.24 mmol), PdCl2(dppf)2-CH2Cl2 (98 mg, 0.12 mmol), DMA (4.5 mL), methyl acrylate (632 μL, 7.1 mmol), and N,N-dicyclohexylmethylamine (748 μL, 3.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (411.6 mg, 74%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.43 (1H, d, J=16.0 Hz), 7.13 (1H, d, J=3.6 Hz), 6.68 (1H, d, J=3.6 Hz), 6.43 (1H, d, J=16.0 Hz), 6.15 (1H, br s), 4.27 (1H, septd, J=6.4, 1.2 Hz), 3.82 (3H, s), 1.28 (6H, d, J=6.4 Hz).
5-Bromo-N-methylthiophene-2-carboxamide (239 mg, 1.1 mmol), tetrabutylammonium chloride (30.6 mg, 0.11 mmol), PdCl2(dppf)2-CH2Cl2 (44.5 mg, 0.05 mmol), DMA (2.2 mL), methyl acrylate (296 μL, 3.3 mmol), and N,N-dicyclohexylmethylamine (347 μL, 1.6 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (16.1 mg, 7%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.72 (1H, d, J=15.6 Hz), 7.39 (1H, d, J=3.6 Hz), 7.19 (1H, d, J=3.6 Hz), 6.31 (1H, d, J=15.6 Hz), 5.96 (1H, br s), 3.80 (3H, s), 3.01 (3H, d, J=4.8 Hz).
5-Bromo-N-(2-methoxyethyl) furan-2-carboxamide (270 mg, 1.1 mmol), tetrabutylammonium chloride (27 mg, 0.097 mmol), PdCl2(dppf)2-CH2Cl2 (40 mg, 0.049 mmol), DMA (2.2 mL), methyl acrylate (411 μL, 4.6 mmol), and N,N-dicyclohexylmethylamine (310 μL, 1.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (221.6 mg, 88%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 7.42 (1H, d, J=16.0 Hz), 7.14 (1H, d, J=3.6 Hz), 6.88 (1H, br s), 6.69 (1H, d, J=3.6 Hz), 6.46 (1H, d, J=16.0 Hz), 3.81 (3H, s), 3.66-3.62 (2H, m), 3.58-3.55 (2H, m), 3.41 (3H, s).
1-(5-Bromothiophen-2-yl)ethan-1-one (700 mg, 3.4 mmol), tetrabutylammonium chloride (95 mg, 0.34 mmol), PdCl2(dppf)2-CH2Cl2 (139.0 mg, 0.17 mmol), DMA (7.0 mL), methyl acrylate (457 μL, 0.17 mmol), and N,N-dicyclohexylmethylamine (1.1 mL, 5.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (304.8 mg, 43%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.73 (1H, d, J=16.0 Hz), 7.60 (1H, d, J=4.0 Hz), 7.24 (1H, d, J=4.0 Hz), 6.39 (1H, d, J=16.0 Hz), 3.81 (3H, s), 2.56 (3H, s).
5-Bromo-N,3-dimethylfuran-2-carboxamide (200 mg, 0.92 mmol), tetrabutylammonium chloride (26 mg, 0.092 mmol), PdCl2(dppf)2-CH2Cl2 (38 mg, 0.046 mmol), DMA (1.5 mL), methyl acrylate (165 μL, 1.8 mmol), and N,N-dicyclohexylmethylamine (292 μL, 1.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (99.6 mg, 48%) as a white solid.
1H NMR (400 MHz, CDCl3) δ7.36 (1H, d, J=15.6 Hz), 6.53 (1H, s), 6.36 (1H, d, J=15.6 Hz), 6.34 (1H, br s), 3.80 (3H, s), 2.98 (3H, d, J=5.2 Hz), 2.39 (3H, s).
5-Bromothiophene-2-sulfonamide (593.2 mg, 2.5 mmol), tetrabutylammonium chloride (68.1 mg, 0.25 mmol), PdCl2(dppf)2-CH2Cl2 (100 mg, 0.12 mmol), DMA (4.0 mL), methyl acrylate (439 μL, 4.9 mmol), and N,N-dicyclohexylmethylamine (780 μL, 3.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (163.7 mg, 27%) as a yellow solid.
1H NMR (400 MHz, CD3OD) δ 7.80 (1H, d, J=16.0 Hz), 7.55 (1H, d, J=4.0 Hz), 7.37 (1H, d, J=4.0 Hz), 6.42 (1H, d, J=16.0 Hz), 3.81 (3H, s).
2-Bromothiophene (235 μL, 2.5 mmol), tetrabutylammonium chloride (68.1 mg, 0.25 mmol), PdCl2(dppf)2-CH2Cl2 (100 mg, 0.12 mmol), DMA (4.0 mL), methyl acrylate (439 μL, 4.9 μmmol), and N,N-dicyclohexylmethylamine (780 μL, 3.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (332.9 mg, 81%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.79 (1H, d, J=16.0 Hz), 7.37 (1H, d, J=5.2 Hz), 7.25 (1H, d, J=3.6 Hz), 7.05 (1H, dd, J=5.2, 3.6 Hz), 6.24 (1H, d, J=16.0 Hz), 3.79 (3H, s).
4-Bromo-N-methylthiophene-2-carboxamide (500 mg, 2.3 mmol), tetrabutylammonium chloride (64 mg, 0.23 mmol), PdCl2(dppf)2-CH2Cl2 (93.0 mg, 0.11 mmol), DMA (4.0 mL), methyl acrylate (407 μL, 4.5 mmol), and N,N-dicyclohexylmethylamine (723 μL, 3.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (213.7 mg, 42%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.63 (1H, s), 7.60 (1H, d, J=16.0 Hz), 7.58 (1H, s), 6.27 (1H, d, J=16.0 Hz), 6.04 (1H, br s), 3.80 (3H, s), 3.01 (3H, d, J=4.8 Hz).
N-[(5-bromofuran-2-yl)methyl]propan-2-amine (600 mg, 2.8 mmol), tetrabutylammonium chloride (78 mg, 0.28 mmol), PdCl2(dppf)2-CH2Cl2 (112 mg, 0.14 mmol), DMA (4.5 mL), methyl acrylate (493 μL, 5.5 mmol), and N,N-dicyclohexylmethylamine (875 μL, 4.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (158 mg, 26%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 7.38 (1H, d, J=15.6 Hz), 6.54 (1H, d, J=3.2 Hz), 6.27 (1H, d, J=15.6 Hz), 6.26 (1H, d, J=3.2 Hz), 3.81 (2H, s), 3.78 (3H, s), 2.85 (1H, septd, J=6.4 Hz), 1.09 (6H, d, J=6.4 Hz).
5-Bromo-N,4-dimethylthiophene-2-carboxamide (200 mg, 0.85 mmol), tetrabutylammonium chloride (24 mg, 0.085 mmol), PdCl2(dppf)2-CH2Cl2 (34.7 mg, 0.043 mmol), DMA (1.2 mL), methyl acrylate (152.5 μL, 1.7 mmol), and N,N-dicyclohexylmethylamine (270 μL, 1.3 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (171.5 mg, 84%) as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.76 (1H, d, J=16.0 Hz), 7.34 (1H, s), 6.94 (1H, br s), 6.20 (1H, d, J=16.0 Hz), 3.79 (3H, s), 2.98 (3H, d, J=4.8 Hz), 2.28 (3H, s).
2-Bromo-1-methyl-1,5,6,7-tetrahydro-4H-indol-4-one (170 mg, 2.3 mmol), tetrabutylammonium chloride (21 mg, 0.085 mmol), PdCl2(dppf)2-CH2Cl2 (31 mg, 0.038 mmol), DMA (0.90 mL), methyl acrylate (135 μL, 1.5 mmol), and N,N-dicyclohexylmethylamine (240 μL, 1.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (154.6 mg, 88%) as a brown solid.
1H NMR (400 MHz, CDCl3) δ 7.56 (1H, d, J=15.6 Hz), 7.00 (1H, s), 6.23 (1H, d, J=15.6 Hz), 3.78 (3H, s), 3.61 (3H, s), 2.79 (2H, t, J=6.4 Hz), 2.47 (2H, t, J=6.4 Hz), 2.17 (2H, quin, J=6.4 Hz).
1-(5-Bromo-1-methyl-1H-pyrrol-2-yl)ethan-1-one (402.7 mg, 1.8 mmol), tetrabutylammonium chloride (66 mg, 0.24 mmol), PdCl2(dppf)2-CH2Cl2 (96.4 mg, 0.12 mmol), dimethylacetamide (1.8 mL), methyl acrylate (423 μL, 4.7 mmol), and N,N-dicyclohexylmethylamine (750 μL, 3.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (153.1 mg, 17%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.64 (1H, d, J=15.6 Hz), 6.95 (1H, d, J=4.4 Hz), 6.60 (1H, d, J=4.4 Hz), 6.37 (1H, d, J=15.6 Hz), 4.01 (3H, s), 3.81 (3H, s), 2.46 (3H, s).
1-(5-Brom-4-methylthiophen-2-yl)ethan-1-one (200 mg, 0.91 mmol), tetrabutylammonium chloride (25.4 mg, 0.091 mmol), PdCl2(dppf)2-CH2Cl2 (37.6 mg, 0.046 mmol), DMA (1.6 mL), methyl acrylate (164 μL, 1.8 mmol), and N,N-dicyclohexylmethylamine (290 μL, 1.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (176.2 mg, 87%) as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.76 (1H, d, J=15.6 Hz), 7.43 (1H, s), 6.29 (1H, d, J=15.6 Hz), 3.80 (3H, s), 2.52 (3H, s), 2.34 (3H, s).
1-(5-Bromo-3-fluorothiophen-2-yl)ethan-1-one (140 mg, 0.46 mmol), tetrabutylammonium chloride (12.8 mg, 0.046 mmol), PdCl2(dppf)2-CH2Cl2 (18.8 mg, 0.023 mmol), DMA (1.0 mL), methyl acrylate (82.5 μL, 0.92 mmol), and N,N-dicyclohexylmethylamine (146 μL, 0.69 mmol) were added and heated under microwave irradiation at 120° C. for 1.5 hours. The obtained solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→7/3), thereby obtaining the title compound (51.3 mg, 49%) as a brown powder.
1H NMR (400 MHz, CDCl3) δ 7.60 (1H, d, J=16.0 Hz), 7.00 (1H, s), 6.39 (1H, d, J=16.0 Hz), 3.81 (3H, s), 2.58 (3H, d, J=2.8 Hz).
5-Bromo-N-(2,4-dimethoxybenzyl)thiophene-2-carboxamide (400 mg, 1.1 mmol), tetrabutylammonium chloride (31 mg, 0.11 mmol), PdCl2(dppf)2-CH2Cl2 (45.7 mg, 0.11 mmol), DMA (2.0 mL), methyl acrylate (201 μL, 2.2 mmol), and N,N-dicyclohexylmethylamine (356 μL, 1.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (99.4 mg, 25%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.67 (1H, d, J=16.0 Hz), 7.41 (1H, d, J=4.0 Hz), 7.19 (1H, d, J=8.4 Hz), 7.13 (1H, d, J=4.0 Hz), 6.85 (1H, t, J=5.6 Hz), 6.43 (1H, d, J=2.4 Hz), 6.41 (1H, dd, J=8.0, 2.4 Hz), 6.26 (1H, d, J=16.0 Hz), 4.49 (2H, d, J=5.6 Hz), 3.81 (3H, s), 3.77 (3H, s), 3.76 (3H, s).
1-(5-Bromo-3-methylthiophen-2-yl)ethan-1-one (216 mg, 0.99 mmol), tetrabutylammonium chloride (14 mg, 0.049 mmol), PdCl2(dppf)2-CH2Cl2 (81 mg, 0.099 mmol), DMA (2.0 mL), methyl acrylate (177 μL, 2.0 mmol), and N,N-dicyclohexylmethylamine (314 μL, 1.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (120.9 mg, 55%) as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.66 (1H, d, J=16.0 Hz), 7.07 (1H, s), 6.35 (1H, d, J=16.0 Hz), 3.81 (3H, s), 2.53 (3H, s), 2.52 (3H, s).
1-(5-Bromo-1,2,4-trimethyl-1H-pyrrol-3-yl)ethan-1-one (120 mg, 0.52 mmol), tetrabutylammonium chloride (14.5 mg, 0.052 μmol), PdCl2(dppf)2-CH2Cl2 (21.2 mg, 0.026 mmol), DMA (0.70 mL), methyl acrylate (93.3 μL, 1.0 mmol), and N,N-dicyclohexylmethylamine (165 μL, 0.78 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (35.2 mg, 29%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.68 (1H, d, J=16.0 Hz), 6.03 (1H, d, J=16.0 Hz), 3.80 (3H, s), 3.59 (3H, s), 2.51 (3H, s), 2.46 (3H, s), 2.40 (3H, s).
1-(5-Bromo-1-ethyl-1H-pyrrol-2-yl)ethan-1-one (500 mg, 2.3 mmol), tetrabutylammonium chloride (64 mg, 0.23 mmol), PdCl2(dppf)2-CH2Cl2 (94.3 mg, 0.12 mmol), DMA (3.5 mL), methyl acrylate (414 μL, 4.6 mmol), and N,N-dicyclohexylmethylamine (733 μL, 3.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (23.2 mg, 5%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.54 (1H, d, J=16.0 Hz), 7.12 (1H, d, J=1.6 Hz), 7.08 (1H, d, J=1.6 Hz), 6.16 (1H, d, J=16.0 Hz), 4.35 (2H, q, J=7.2 Hz), 3.77 (3H, s), 2.46 (3H, s), 1.37 (3H, t, J=7.2 Hz).
(5-Bromothiophen-2-yl)(cyclopropyl)methanone (56 mg, 0.24 mmol), tetrabutylammonium chloride (3.4 mg, 0.012 mmol), PdCl2(dppf)2-CH2Cl2 (20 mg, 0.024 mmol), DMA (0.60 mL), methyl acrylate (43.4 μL, 0.48 mmol), and N,N-dicyclohexylmethylamine (77 μL, 0.36 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (34 mg, 60%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.74 (1H, d, J=16.0 Hz), 7.72 (1H, d, J=4.0 Hz), 7.27 (1H, d, J=4.0 Hz), 6.39 (1H, d, J=16.0 Hz), 3.81 (3H, s), 2.51 (1H, tt, J=8.0, 4.4 Hz), 1.28-1.25 (2H, m), 1.08-1.04 (2H, m).
2-(5-Bromothiophen-2-yl)-2-methyl-1,3-dioxolane (180 mg, 0.72 mmol), tetrabutylammonium chloride (20 mg, 0.072 mmol), PdCl2(dppf)2-CH2Cl2 (29.4 mg, 0.036 mmol), DMA (1.1 mL), methyl acrylate (129 μL, 1.4 mmol), and N,N-dicyclohexylmethylamine (232 μL, 1.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (135.5 mg, 74%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.71 (1H, d, J=15.6 Hz), 7.10 (1H, d, J=3.6 Hz), 6.97 (1H, d, J=3.6 Hz), 6.18 (1H, d, J=15.6 Hz), 4.08-4.02 (m, 2H), 3.98-3.95 (m, 2H), 3.78 (3H, s), 1.76 (s, 3H).
5-Bromothiophene-2-carbonitrile (289 μL, 2.7 mmol), tetrabutylammonium chloride (74 mg, 0.27 mmol), PdCl2(dppf)2-CH2Cl2 (109 mg, 0.13 mmol), DMA (3.3 mL), methyl acrylate (477 μL, 5.3 mmol), and N,N-dicyclohexylmethylamine (845 μL, 4.0 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (77.6 mg, 15%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.71 (1H, d, J=16.0 Hz), 7.55 (1H, d, J=4.0 Hz), 7.23 (1H, d, J=4.0 Hz), 6.36 (1H, d, J=16.0 Hz), 3.82 (3H, s).
2-(5-Bromo-3-methylthiophen-2-yl)-2-methyl-1,3-dioxolone (306.1 mg, 1.2 mmol), PdCl2(dppf)2-CH2Cl2 (48.8 mg, 0.0060 mmol), and tetrabutylammonium chloride (27.8 mg, 0.12 mmol) were added to a flask. DMA (1.7 mL), N,N-dicyclohexylmethylamine (500 μL, 2.4 mmol), and methyl acrylate (210 μL, 2.3 mmol) were added, and the mixture was heated under microwave irradiation at 130° C. for 3 hours. Further, the mixture was heated under microwave irradiation at 130° C. for 1 hour, and the reaction solution was returned to room temperature. The reaction solution was diluted with ethyl acetate, washed with water and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=98/2→77/23), thereby obtaining the title compound (160.8 mg, 52%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.61 (1H, d, J=15.6 Hz), 6.92 (1H, s), 6.11 (1H, d, J=15.6 Hz), 4.07-3.98 (2H, m), 3.94-3.88 (2H, m), 3.74 (3H, s), 2.23 (3H, s), 1.70 (3H, s).
Methyl acrylate (250 μL, 2.8 mmol) and N,N-dicyclohexylamine (600 μL, 2.8 mmol) were added to a DMA (1.8 mL) solution of 2-bromo-4,5-dihydro-6H-thieno[2,3-c]pyrrol-6-one (301.3 mg, 1.4 mmol), PdCl2(dppf)2-CH2Cl2 (59.4 mg, 0.073 mmol), and tetrabutylammonium chloride (40.3 mg, 0.15 mmol), and the mixture was heated under microwave irradiation at 130° C. for 3 hours. The reaction solution was cooled to room temperature, and ethyl acetate and 1M hydrochloric acid were added to separate the organic layer and the aqueous layer. The aqueous layer was extracted with ethyl acetate, and the combined organic layer was washed with saturated saline and dried over sodium sulfate. The solvent was removed by distillation under reduced pressure, followed by purification by silica gel column chromatography (hexane/ethyl acetate (v/v)=19/81→0/100), thereby obtaining the title compound (171 mg, 55%) as an orange solid.
1H NMR (400 MHz, CDCl3) δ 7.77 (1H, d, J=15.6 Hz), 7.18 (1H, s), 6.54 (1H, br s), 6.37 (1H, d, J=15.6 Hz), 4.38 (2H, s), 3.81 (3H, s).
1-(5-Bromofuran-2-yl)ethan-1-one (220 mg, 1.16 mmol), tetrabutylammonium chloride (16 mg, 0.058 mmol), PdCl2(dppf)2-CH2Cl2 (94 mg, 0.115 mmol), DMA (2.0 mL), methyl acrylate (206 μL, 2.3 mmol), and N,N-dicyclohexylmethylamine (364 μL, 1.72 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (90.0 mg, 40%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.43 (1H, d, J=16.0 Hz), 7.17 (1H, d, J=3.6 Hz), 6.69 (1H, d, J=3.6 Hz), 6.54 (1H, d, J=16.0 Hz), 3.79 (1H, s), 2.49 (3H, s).
1-(4-Bromothiophen-2-yl)ethan-1-one (200 mg, 0.98 mmol), tetrabutylammonium chloride (13.6 mg, 0.049 mmol), PdCl2(dppf)2-CH2Cl2 (80 mg, 0.098 mmol), DMA (2.0 mL), methyl acrylate (176 μL, 2.0 mmol), and N,N-dicyclohexylmethylamine (310 μL, 1.47 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (114.3 mg, 56%) as an orange solid.
1H NMR (400 MHz, CDCl3) δ 7.82 (1H, d, J=1.2 Hz), 7.74 (1H, d, J=1.2 Hz), 7.62 (1H, d, J=16.0 Hz), 6.32 (1H, d, J=16.0 Hz), 3.81 (3H, s), 2.59 (3H, s).
1-(5-Bromothiophen-3-yl)ethan-1-one (380 mg, 1.9 mmol), tetrabutylammonium chloride (25.7 mg, 0.093 mmol), PdCl2(dppf)2-CH2Cl2 (151 mg, 0.19 mmol), DMA (3.8 mL), methyl acrylate (344 μL, 3.7 mmol), and N,N-dicyclohexylmethylamine (586 μL, 2.8 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (151.8 mg, 39%) as a pale green powder.
1H NMR (400 MHz, CDCl3) δ 8.03 (1H, s), 7.73 (1H, d, J=16.0 Hz), 7.64 (1H, br s), 6.27 (1H, d, J=16.0 Hz), 3.80 (3H, s), 2.52 (3H, s).
4-Bromo-1-methyl-1H-pyrrole-2-carbonitrile (131.9 mg, 0.71 mmol), tetrabutylammonium chloride (19.7 mg, 0.071 mmol), PdCl2(dppf)2-CH2Cl2 (58 mg, 0.071 mmol), DMA (1.2 mL), methyl acrylate (128 μL, 1.4 mmol), and N,N-dicyclohexylmethylamine (227 μL, 1.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (33.5 mg, 25%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.48 (1H, d, J=16.0 Hz), 7.01 (1H, d, J=1.6 Hz), 6.96 (1H, d, J=1.6 Hz), 6.13 (1H, d, J=16.0 Hz), 3.80 (3H, s), 3.77 (3H, s).
1-(2-Bromothiophen-3-yl)ethan-1-one (128.8 mg, 0.63 mmol), tetrabutylammonium chloride (8.8 mg, 0.032 mmol), PdCl2(dppf)2-CH2Cl2 (51.4 mg, 0.065 mmol), DMA (1.3 mL), methyl acrylate (113 μL, 1.3 mmol), and N,N-dicyclohexylmethylamine (200 μL, 0.95 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (62.1 mg, 47%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) 8.51 (1H, d, J=16.0 Hz), 7.40 (1H, d, J=5.6 Hz), 7.28 (1H, d, J=5.6 Hz), 6.34 (1H, d, J=16.0 Hz), 3.78 (3H, s), 2.54 (3H, s).
2-(5-Bromofuran-2-yl)-2-methyl-1,3-dioxolane (200 mg, 0.86 mmol), tetrabutylammonium chloride (12 mg, 0.043 mmol), PdCl2(dppf)2-CH2Cl2 (70.1 mg, 0.086 mmol), DMA (2.0 mL), methyl acrylate (160 μL, 1.7 mmol), and N,N-dicyclohexylmethylamine (272 μL, 1.3 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (168.8 mg, 83%) as an oily yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.39 (1H, d, J=15.6 Hz), 6.52 (1H, d, J=3.6 Hz), 6.39 (1H, d, J=3.6 Hz), 6.32 (1H, d, J=15.6 Hz), 4.09-4.05 (2H, m), 4.04-4.00 (2H, m), 3.78 (3H, s), 1.75 (3H, s).
2-(5-Bromothiophen-3-yl)-2-methyl-1,3-dioxolane (160 mg, 0.64 mmol), tetrabutylammonium chloride (8.9 mg, 0.032 mmol), PdCl2(dppf)-CH2Cl2 (52.4 mg, 0.064 mmol), DMA (1.3 mL), methyl acrylate (115 μL, 1.3 mmol), and N,N-dicyclohexylmethylamine (203 μL, 0.96 mmol) were used as raw materials, and the same operation was performed as in Reference Example 103, thereby obtaining the title compound (137.7 mg, 84%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.72 (1H, d, J=15.6 Hz), 7.31 (1H, s), 7.21 (1H, s), 6.22 (1H, d, J=15.6 Hz), 4.06-4.02 (2H, m), 3.89-3.86 (2H, m), 3.79 (3H, s), 1.66 (3H, s).
A THF (2.0 mL) solution of potassium tert-butoxide (123.4 mg, 1.1 mmol) and triethyl phosphonoacetate (220 μL, 1.1 mmol) was stirred at −5° C. for 30 minutes. Then, thiazole-5-carboaldehyde (100 mg, 0.88 mmol) was added, and the mixture was stirred at −5° C. for 2 hours, and then stirred at room temperature for 21 hours. The reaction solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→7/3), thereby obtaining the title compound (143.5 mg, 89%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 8.80 (1H, s), 8.01 (1H, s), 7.82 (1H, d, J=15.6 Hz), 6.26 (1H, d, J=15.6 Hz), 4.26 (2H, q, J=7.2 Hz), 1.33 (3H, t, J=7.2 Hz).
Methyl (triphenylphosphoranylidene)acetate (424.2 mg, 1.3 mmol) was added to a toluene (1.5 mL) solution of 5-(2-methyl-1,3-dioxolan-2-yl)thiazole-2-carbaldehyde (85.2 mg, 0.42 mmol), and the mixture was stirred at 120° C. for 1 hour. The reaction solution was returned to room temperature, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=81/19→62/38), thereby obtaining the title compound (111.5 mg, quant.) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.79 (1H, s), 7.70 (1H, d, J=15.6 Hz), 6.65 (1H, d, J=15.6 Hz), 4.14-4.04 (2H, m), 3.99-3.91 (2H, m), 3.82 (3H, s), 1.78 (3H, s).
Methyl (triphenylphosphoranylidene)acetate (160.7 mg, 0.48 mmol) was added to a toluene (1.0 mL) solution of 4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiazole-2-carbaldehyde (32.5 mg, 0.15 mmol), and the mixture was stirred at 120° C. for 1.5 hours. The reaction solution was returned to room temperature, the solvent was distilled under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=86/14→65/35), thereby obtaining the title compound (34.6 mg, 85%) as an oily transparent orange substance.
1H NMR (400 MHz, CDCl3) δ 7.63 (1H, d, J=15.6 Hz), 6.60 (1H, d, J=15.6 Hz), 4.08-4.02 (2H, m), 3.94-3.86 (2H, m), 3.80 (3H, s), 2.49 (3H, s), 1.74 (3H, s).
TEA (168 μL, 1.2 mmol) was added to a 1,4-dioxane/water (3/1) (1.0 mL) solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (165 mg, 0.36 mmol), methyl (E)-3-[5-(methylcarbamoyl)furan-2-yl]acrylate (50 mg, 0.24 mmol), and [RhCl(cod)]2 (5.9 mg, 0.012 mmol), and the mixture was stirred under heating and refluxing for 14 hours. The obtained solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=3/2→2/3), thereby obtaining the title compound (22.9 mg, 18%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, d, J=8.0 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.28-7.21 (3H, m), 7.14-7.07 (2H, m), 6.98 (1H, d, J=3.2 Hz), 6.37 (1H, br s), 6.15 (1H, t, J=3.2 Hz), 4.55-4.49 (2H, m), 4.04-3.99 (1H, m), 3.87-3.84 (1H, m), 3.80-3.73 (1H, m), 3.62 (3H, br s), 3.12-3.00 (3H, m), 2.95-2.94 (3H, m), 2.30 (3H, br s), 1.76-1.66 (1H, m), 1.53-1.41 (1H, m), 1.09 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (240 mg, 0.52 mmol), methyl (E)-3-[5-(pyrrolidine-1-carbonyl)furan-2-yl]acrylate (84 mg, 0.34 mmol), [RhCl(cod)]2 (17.4 mg, 0.035 mmol), 1,4-dioxane/DMA/water (3/3/1) (0.7 mL), and TEA (74 μL, 0.53 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (85.0 mg, 50%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.29-7.12 (5H, m), 6.97 (1H, d, J=3.2 Hz), 6.11 (1H, d, J=3.2 Hz), 4.57-4.53 (2H, m), 4.03-3.98 (1H, m), 3.81 (1H, d, J=14.4 Hz), 3.78-3.67 (3H, m), 3.61-3.58 (5H, m), 3.14-3.10 (1H, m), 2.99-2.87 (2H, m), 2.32 (3H, s), 1.99-1.95 (2H, m), 1.88-1.85 (2H, m), 1.74-1.64 (1H, m), 1.50-1.42 (1H, m), 1.08 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (206 mg, 0.45 mmol), methyl (E)-3-[5-(isopropylcarbamoyl) furan-2-yl]acrylate (70 mg, 0.3 mmol), [RhCl(cod)]2 (15 mg, 0.030 mmol), 1,4-dioxane/water (6/1) (0.7 mL), and TEA (152 μL, 1.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (38.2 mg, 22%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, t, J=8.0 Hz), 7.21 (1H, d, J=8.0 Hz), 7.16-7.08 (3H, m), 6.98 (1H, d, J=3.6 Hz), 6.14-6.10 (1H, m), 6.05 (1H, br s), 4.56-4.51 (2H, m), 4.26-4.19 (1H, m), 4.03-4.00 (1H, m), 3.87-3.74 (2H, m), 3.64 (3H, s), 3.07-2.99 (2H, m), 2.88-2.85 (1H, m), 2.33 (3H, br s), 1.76-1.65 (1H, m), 1.51-1.42 (1H, m), 1.26-1.22 (6H, m), 1.09-1.08 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (240 mg, 0.52 mmol), methyl (E)-3-[5-(methylcarbamoyl)thiophen-2-yl]acrylate (79 mg, 0.35 mmol), [RhCl(cod)]; (17.4 mg, 0.035 mmol), 1,4-dioxane/DMA/water (3/3/1) (0.7 mL), and TEA (74 μL, 0.53 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (48.7 mg, 25%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.29-7.19 (3H, m), 7.14 (2H, br s), 7.07 (1H, d, J=6.8 Hz), 6.78-6.77 (1H, m), 5.99 (1H, br s), 4.69 (1H, t, J=7.6 Hz), 4.56 (1H, dd, J=14.0, 5.2 Hz), 4.02-3.95 (1H, m), 3.82-3.69 (2H, m), 3.60 (3H, s), 3.09 (1H, dd, J=16.0, 7.6 Hz), 3.01-2.90 (5H, m), 2.34 (3H, br s), 1.69-1.62 (1H, m), 1.46-1.38 (1H, m), 1.06 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (192 mg, 0.42 mmol), methyl (E)-3-{5-((2-methoxyethyl)carbamoyl) furan-2-yl}acrylate (70 mg, 0.28 mmol), [RhCl(cod)]2 (13.8 mg, 0.028 mmol), 1,4-dioxane/water (6/1) (0.7 mL), and TEA (60 μL, 0.42 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (11.1 mg, 7%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, t, J=8.0 Hz), 7.23 (1H, d, J=8.0 Hz), 7.16-7.09 (3H, m), 6.99 (1H, d, J=3.6 Hz), 6.55 (1H, br s), 6.12 (1H, t, J=3.6 Hz), 4.57-4.51 (2H, m), 4.04-4.00 (1H, m), 3.87-3.71 (2H, m), 3.63 (3H, s), 3.60-3.51 (4H, m), 3.37 (3H, s), 3.11-2.85 (3H, m), 2.33 (3H, br s), 1.78-1.67 (1H, m), 1.51-1.41 (1H, m), 1.08 (3H, t, J=7.6 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (274.4 mg, 0.6 mmol), methyl (E)-3-(5-acetylthiophen-2-yl)acrylate (105 mg, 0.5 mmol), [RhCl(cod)]2 (12.3 mg, 0.025 mmol), 1,4-dioxane/water (7/1) (1.0 mL), and TEA (210 μL, 1.5 μmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (138.0 mg, 50%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.50 (1H, d, J=4.0 Hz), 7.27-7.20 (2H, m), 7.17-7.12 (2H, m), 7.08 (1H, d, J=8.4 Hz), 6.87 (1H, br t, J=2.4 Hz), 4.72 (1H, t, J=7.6 Hz), 4.58-4.56 (1H, m), 4.03-3.96 (1H, m), 3.83-3.69 (2H, m), 3.61 (3H, s), 3.13-2.91 (3H, m), 2.48 (3H, br s), 2.34 (3H, br s), 1.73-1.63 (1H, m), 1.47-1.39 (1H, m), 1.07 (3H, t, J=7.6 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (247 mg, 0.54 mmol), methyl (E)-3-[4-methyl-5-(methylcarbamoyl)furan-2-yl]acrylate (100 mg, 0.45 mmol), [RhCl(cod)]2 (11.3 mg, 0.023 mmol), 1,4-dioxane/water (6/1) (1.0 mL), and TEA (189 μL, 1.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (48.2 mg, 19%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.27-7.19 (3H, m), 7.13 (1H, d, J=7.6 Hz), 7.10-7.06 (1H, m), 6.27 (1H, br s), 5.98 (1H, d, J=3.2 Hz), 4.49-4.44 (2H, m), 4.05-3.98 (1H, m), 3.89-3.72 (2H, m), 3.63 (3H, s), 3.09-2.84 (6H, m), 2.34-2.30 (6H, m), 1.78-1.59 (1H, m), 1.52-1.41 (1H, m), 1.09 (3H, t, J=7.2 Hz).
TEA (84 μL, 0.6 mmol) was added to a 1,4-dioxane/water (1/1) (0.8 mL) solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (137.2 mg, 0.3 mmol), methyl (E)-3-(5-sulfamoylthiophen-2-yl)acrylate (50 mg, 0.2 mmol), and [RhCl(cod)]2 (9.9 mg, 0.02 mmol), and the mixture was stirred under microwave irradiation at 120° C. for 1 hour. The obtained solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=4/1→3/2), thereby obtaining the title compound (98.9 mg, 85%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.84 (1H, br d, J=8.0 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.42 (1H, d, J=4.0 Hz), 7.27-7.19 (2H, m), 7.15-7.11 (3H, m), 6.78 (1H, d, J=4.0 Hz), 4.71 (1H, t, J=8.0 Hz), 4.51 (1H, d, J=14.4 Hz), 4.03-3.97 (1H, m), 3.83-3.82 (1H, m), 3.77-3.69 (1H, m), 3.61 (3H, s), 3.11-2.95 (3H, m), 2.30 (3H, s), 1.74-1.63 (1H, m), 1.51-1.43 (1H, m), 1.08-1.07 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (247 mg, 0.54 mmol), methyl (E)-3-(thiophen-2-yl)acrylate (76 mg, 0.45 mmol), [RhCl(cod)]2 (11.3 mg, 0.023 mmol), 1,4-dioxane/water (3/1) (1.0 mL), and TEA (189 μL, 1.4 mmol) were used as raw materials, and the same operation was performed as in Reference Example 123, thereby obtaining the title compound (133 mg, 60%) as a white solid.
1H NMR (400 MHz, CDCl3) 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.26-7.12 (5H, m), 7.03 (1H, d, J=14.4 Hz), 6.89 (1H, br t, J=4.0 Hz), 6.81 (1H, br t, J=4.0 Hz), 4.71 (1H, t, J=7.6 Hz), 4.60-4.57 (1H, m), 4.01-3.92 (1H, m), 3.80-3.68 (2H, m), 3.59 (3H, br s), 3.13-3.06 (1H, m), 3.02-2.87 (2H, m), 2.36 (3H, br s), 1.71-1.59 (1H, m), 1.44-1.32 (1H, m), 1.07-1.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (137.2 mg, 0.3 mmol), methyl (E)-3-[5-(methylcarbamoyl)thiophen-3-yl]acrylate (45.1 mg, 0.2 mmol), [RhCl(cod)]2 (9.9 mg, 0.02 mmol), 1,4-dioxane/water (1/1) (0.8 mL), and TEA (84 μL, 0.6 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (77.5 mg, 70%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.85 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.31-7.30 (1H, m), 7.25 (1H, t, J=8.0 Hz), 7.21 (1H, d, J=8.0 Hz), 7.11-7.05 (4H, m), 6.37 (1H, br s), 4.51-4.47 (2H, m), 4.02-3.95 (1H, m), 3.84-3.70 (2H, m), 3.58 (3H, s), 3.05-2.92 (3H, m), 2.89 (3H, d, J=4.8 Hz), 2.28 (3H, s), 1.74-1.61 (1H, m), 1.50-1.39 (1H, m), 1.08-1.07 (3H, m).
(R)-4-ethyl-2-(2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (226.4 mg, 0.5 mmol), methyl (E)-3-[3-methyl-5-(methylcarbamoyl)thiophen-2-yl]acrylate (80 mg, 0.3 mmol), [RhCl(cod)]2 (16.3 mg, 0.03 mmol), 1,4-dioxane/water (1/1) (1.6 mL), and TEA (138.4 μL, 1.0 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (148.1 mg, 78%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, br d, J=8.0 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.26 (1H, d, J=8.0 Hz), 7.23-7.19 (1H, m), 7.17 (1H, br s), 7.14-7.11 (2H, m), 7.05 (1H, br d, J=5.6 Hz), 6.08 (1H, br s), 4.72 (1H, t, J=8.0 Hz), 4.56-4.55 (1H, m), 4.00-3.95 (1H, m), 3.78-3.68 (2H, m), 3.59 (3H, s), 2.99 (2H, dd, J=7.6, 7.6 Hz), 2.94-2.90 (4H, m), 2.33 (3H, br s), 2.10 (3H, s), 1.73-1.60 (1H, m), 1.45-1.38 (1H, m), 1.07-1.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (206 mg, 0.45 mmol), ethyl (E)-3-(thiazol-5-yl)acrylate (55 mg, 0.3 mmol), [RhCl(cod)]2 (15 mg, 0.03 mmol), 1,4-dioxane/water (1/1) (1.0 mL), and TEA (126 μL, 0.9 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (97.3 mg, 63%) as a pale red solid.
1H NMR (400 MHz, CDCl3) δ 8.80 (1H, s), 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.63 (1H, d, J=3.6 Hz), 7.52 (1H, td, J=7.6, 2.0 Hz), 7.25 (1H, td, J=7.6, 1.2 Hz), 7.20 (1H, dd, J=8.0, 0.8 Hz), 7.17-7.12 (2H, m), 7.08 (1H, d, J=7.6 Hz), 4.77 (1H, t, J=8.0 Hz), 4.57 (1H, dd, J=14.0, 5.2 Hz), 4.09-3.98 (3H, m), 3.83-3.69 (2H, m), 3.11-2.91 (3H, m), 2.34 (3H, br s), 1.71-1.65 (1H, m), 1.46-1.40 (1H, m), 1.16 (3H, t, J=7.2 Hz), 1.09-1.05 (3H, m)).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (206 mg, 0.5 mmol), methyl (E)-3-(1-methyl-4-oxo-4,5,6,7-tetrahydro-1H-indol-2-yl)acrylate (70 mg, 0.3 mmol), [RhCl(cod)]2 (15 mg, 0.03 mmol), 1,4-dioxane/water (1/1) (1.0 mL), and TEA (126 μL, 0.9 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (149.8 mg, 91%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.87-7.82 (1H, m), 7.55-7.50 (1H, m), 7.28-7.19 (2H, m), 7.13-7.10 (1H, m), 7.06-7.01 (1H, m), 6.96 (1H, s), 6.48 (1H, d, J=4.0 Hz), 4.52-4.51 (1H, m), 4.41 (1H, t, J=8.0 Hz), 4.00-3.95 (1H, m), 3.80-3.72 (2H, m), 3.61 (1H, s), 3.23 (3H, br s), 3.04-2.87 (2H, m), 2.80-2.73 (1H, m), 2.67-2.62 (2H, m), 2.46-2.42 (2H, m), 2.34 (3H, br s), 2.14-2.10 (2H, m), 1.75-1.62 (1H, m), 1.50-1.39 (1H, m), 1.11-1.04 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (206 mg, 0.5 mmol), methyl (E)-3-(5-acetyl-1-methyl-1H-pyrrol-2-yl)acrylate (62.2 mg, 0.3 mmol), [RhCl(cod)]2 (15 mg, 0.03 mmol), 1,4-dioxane/water (1/1) (1.0 mL), and TEA (126 μL, 0.9 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (129.3 mg, 80%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.25 (1H, t, J=7.6 Hz), 7.20 (1H, d, J=7.6 Hz), 7.12-7.10 (1H, m), 7.02-6.92 (3H, m), 6.13 (1H, d, J=4.4 Hz), 4.57-4.46 (2H, m), 4.00-3.93 (1H, m), 3.80-3.73 (1H, m), 3.68-3.65 (4H, m), 3.63 (3H, br s), 3.05-2.81 (3H, m), 2.39 (3H, s), 2.34-2.31 (3H, m), 1.74-1.61 (1H, m), 1.47-1.40 (1H, m), 1.09-1.05 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (206 mg, 0.5 mmol), methyl (E)-3-(5-acetyl-3-methylthiophen-2-yl)acrylate (67.3 mg, 0.3 mmol), [RhCl(cod)]2 (15 mg, 0.03 mmol), 1,4-dioxane/water (1/1) (2.0 mL), and TEA (126 μL, 0.9 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (123.3 mg, 74%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ7.87 (1H, dt, J=8.0, 2.0 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.38 (1H, s), 7.28-7.20 (2H, m), 7.17-7.12 (2H, m), 7.05 (1H, d, J=8.0 Hz), 4.74-4.73 (1H, m), 4.58-4.55 (1H, m), 4.03-3.95 (1H, m), 3.80-3.66 (2H, m), 3.60 (3H, br s), 3.07-2.86 (3H, m), 2.46 (3H, br s), 2.35 (3H, br s), 2.16 (3H, s), 1.74-1.60 (1H, m), 1.46-1.36 (1H, m), 1.08-1.07 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (75.5 mg, 0.17 mmol), methyl (E)-3-(5-acetyl-4-fluorothiophen-2-yl)acrylate (51.3 mg, 0.23 mmol), [RhCl(cod)]2 (5.4 mg, 0.011 mmol), 1,4-dioxane/water (1/1) (0.9 mL), and TEA (69 μL, 0.49 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (53.6 mg, 56%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, td, J=8.0, 1.2 Hz), 7.21 (1H, dd, J=8.0, 1.2 Hz), 7.18-7.07 (3H, m), 6.64 (1H, s), 4.61-4.53 (2H, m), 4.06-3.98 (1H, m), 3.87-3.69 (2H, m), 3.63 (3H, s), 3.09-2.94 (3H, m), 2.50 (3H, br s), 2.35 (3H, br s), 1.74-1.65 (1H, m), 1.49-1.42 (1H, m), 1.08-1.07 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (150 mg, 0.328 mmol), methyl (E)-3-{5-[(2,4-dimethoxybenzyl)carbamoyl]thiophen-2-yl}acrylate (80 mg, 0.22 mmol), [RhCl(cod)]2 (10.8 mg, 0.022 mmol), 1,4-dioxane/water (1/1) (1.0 mL), and TEA (92.2 μL, 0.66 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (112.4 mg, 74%) as an oily pale brown substance.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, br t, J=8.0 Hz), 7.27-7.24 (2H, m), 7.22-7.18 (2H, m), 7.13 (2H, br s), 7.04 (1H, br d, J=8.0 Hz), 6.76 (1H, br t, J=3.6 Hz), 6.45-6.40 (3H, m), 4.67 (1H, t, J=7.6 Hz), 4.56-4.55 (1H, m), 4.47 (2H, d, J=5.6 Hz), 3.99-3.93 (1H, m), 3.84-3.67 (8H, m), 3.59 (3H, s), 3.09-2.88 (3H, m), 2.33 (3H, s), 1.67-1.58 (1H, m), 1.44-1.36 (1H, m), 1.04-1.03 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (150 mg, 0.3 mmol), methyl (E)-3-(5-acetyl-4-methylthiophen-2-yl)acrylate (50 mg, 0.2 mmol), [RhCl(cod)]2 (10.8 mg, 0.02 mmol), 1,4-dioxane/water (1/1) (1.0 mL), and TEA (92.2 LL, 0.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (77.9 mg, 64%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.89-7.86 (1H, m), 7.52 (1H, br t, J=8.0 Hz), 7.28-7.08 (5H, m), 6.69 (1H, br s), 4.66 (1H, t, J=7.6 Hz), 4.60-4.48 (1H, m), 4.04-3.97 (1H, m), 3.85-3.70 (2H, m), 3.62-3.60 (3H, m), 3.12-2.87 (3H, m), 2.45-2.42 (3H, m), 2.35-2.31 (3H, m), 1.73-1.63 (1H, m), 1.47-1.39 (1H, m), 1.08-1.05 (3H, m)).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (93.3 mg, 0.20 mmol), methyl (E)-3-(4-acetyl-1,3,5-trimethyl-1H-pyrrol-2-yl)acrylate (30 mg, 0.14 mmol), [RhCl(cod)]2 (7.0 mg, 0.014 mmol), 1,4-dioxane/water (1/1) (0.8 mL), and TEA (57 μL, 0.41 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (20.1 mg, 26%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89-7.85 (1H, m), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.11 (1H, br d, J=8.0 Hz), 7.01-6.93 (2H, m), 4.85-4.80 (1H, m), 4.55-4.51 (1H, m), 3.99-3.94 (1H, m), 3.80-3.69 (2H, m), 3.65 (3H, br s), 3.25-3.17 (4H, m), 2.99-2.88 (2H, m), 2.43-2.42 (6H, m), 2.34-2.32 (3H, m), 2.22 (3H, s), 1.75-1.61 (1H, m), 1.48-1.32 (1H, m), 1.07-1.05 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (123.5 mg, 0.27 mmol), methyl (E)-3-(5-acetyl-1-ethyl-1H-pyrrol-2-yl)acrylate (40 mg, 0.18 mmol), [RhCl(cod)]2 (9.0 mg, 0.018 mmol), 1,4-dioxane/water (1/1) (0.8 mL), and TEA (75.5 μL, 0.54 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (37.2 mg, 37%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.15-7.08 (3H, m), 6.70 (1H, dd, J=4.8, 2.0 Hz), 6.62 (1H, dd, J=4.8, 2.0 Hz), 4.55 (1H, d, J=14.0 Hz), 4.35 (1H, t, J=8.0 Hz), 4.26 (1H, q, J=7.2 Hz), 4.03-3.99 (1H, m), 3.84-3.70 (2H, m), 3.60 (3H, s), 3.00-2.93 (2H, m), 2.90-2.82 (1H, m), 2.36 (3H, s), 2.33 (3H, s), 1.73-1.63 (1H, m), 1.47-1.39 (1H, m), 1.30 (3H, t, J=7.2 Hz), 1.07 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (99 mg, 0.2 mmol), methyl (E)-3-[5-(cyclopropanecarbonyl)thiophen-2-yl]acrylate (34 mg, 0.14 mmol), [RhCl(cod)]2 (7.1 mg, 0.014 mmol), 1,4-dioxane/water (1/1) (0.8 mL), and TEA (60 μL, 0.43 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (45.5 mg, 56%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.63 (1H, d, J=3.6 Hz), 7.52 (1H, td, J=7.6, 1.6 Hz), 7.25 (1H, dd, J=7.6, 0.8 Hz), 7.22 (1H, br d, J=7.6 Hz), 7.15 (2H, br s), 7.06 (1H, d, J=10.4 Hz), 6.90-6.88 (1H, m), 4.73 (1H, t, J=7.6 Hz), 4.60-4.54 (1H, m), 4.00-3.97 (1H, m), 3.81-3.77 (1H, m), 3.76-3.71 (1H, m), 3.61 (3H, s), 3.14-2.89 (3H, m), 2.47-2.43 (1H, m), 2.35 (3H, br s), 1.70-1.61 (1H, m), 1.44-1.39 (1H, m), 1.21-1.17 (2H, m), 1.06 (3H, t, J=7.2 Hz), 1.00-0.96 (2H, m).
TEA (132 μL, 0.95 mmol) was added under argon atmosphere to a 1,4-dioxane/water (1/1) (1.7 mL) mixed solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (216 mg, 0.47 mmol), methyl (E)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl)]acrylate (80 mg, 0.32 mmol), and [RhCl(cod)]2 (15.5 mg, 0.032 mmol), and the mixture was heated under microwave irradiation at 140° C. for 2 hours. Water was added to the mixture, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→7/3), thereby obtaining the title compound (90.9 mg, 49%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, br t, J=8.0 Hz), 7.21 (1H, dd, J=8.0, 1.6 Hz), 7.14 (2H, br s), 7.06 (1H, s), 6.81 (1H, d, J=3.6 Hz), 6.62 (1H, d, J=3.6 Hz), 4.63 (1H, t, J=8.0 Hz), 4.58 (1H, d, J=14.0 Hz), 4.03-3.96 (3H, m), 3.93-3.90 (2H, m), 3.81-3.77 (1H, m), 3.73 (1H, dd, J=15.2, 10.8 Hz), 3.59 (3H, s), 3.10-3.07 (1H, m), 3.00-2.93 (2H, m), 2.35 (3H, s), 1.76-1.61 (1H, m), 1.70 (3H, s), 1.49-1.41 (1H, m), 1.11.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (137.2 mg, 0.3 mmol), methyl (E)-3-(5-cyanothiophen-2-yl)acrylate (38.6 mg, 0.2 mmol), [RhCl(cod)]2 (9.9 mg, 0.02 mmol), 1,4-dioxane/water (1/1) (0.8 mL), and TEA (83.9 μL, 0.6 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (22.2 mg, 21%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.44 (1H, dd, J=4.0, 0.8 Hz), 7.28-7.16 (3H, m), 7.13-7.10 (2H, m), 6.85 (1H, br d, J=4.0 Hz), 4.73 (1H, t, J=7.6 Hz), 4.58-4.52 (1H, m), 4.06-3.98 (1H, m), 3.88-3.81 (1H, m), 3.76-3.69 (1H, m), 3.63 (3H, s), 3.13-2.93 (3H, m), 2.34 (3H, br s), 1.77-1.64 (1H, m), 1.50-1.39 (1H, m), 1.12-1.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (499.7 mg, 1.1 mmol), methyl (E)-3-[4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]acrylate (146.8 mg, 1.1 mmol), and [RhCl(cod)]2 (17.1 mg, 0.035 mmol) were purged with an argon atmosphere. 1,4-Dioxane/water (1/1) (1.2 mL) and TEA (250 μL, 1.8 mmol) were added, and the mixture was heated under microwave irradiation at 120° C. for 1.5 hours. The reaction solution was returned to room temperature, diluted with ethyl acetate, and washed with water and saturated saline, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane/TEA=23/75/2), thereby obtaining the title compound (204.3 mg, 62%) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.28-7.24 (1H, m), 7.22 (1H, d, J=8.0 Hz), 7.14 (2H, s), 7.06 (1H, s), 6.45 (1H, s), 4.60-4.53 (2H, m), 4.06-3.95 (3H, m), 3.92-3.86 (2H, m), 3.79 (1H, br d, J=14.0 Hz), 3.74-3.72 (1H, m), 3.58 (3H, s), 3.05-3.01 (1H, m), 3.00-2.89 (2H, m), 2.35 (3H, s), 2.18 (3H, s), 1.74-1.64 (1H, m), 1.67 (3H, s), 1.52-1.42 (1H, m), 1.09-1.08 (3H, m).
TEA (66 μL, 0.47 mmol) was added to a 1,4-dioxane/water (2/1) (0.5 mL) solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (56.7 mg, 0.13 mmol), methyl (E)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiazol-2-yl]acrylate (21.8 mg, 0.085 mml 1), and [RhCl(cod)]2 (7.1 mg, 0.016 mmol), and the mixture was heated under microwave irradiation at 50° C. for 4 hours. The reaction solution was returned to room temperature, diluted with ethyl acetate, washed with water, and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=91/9→70/30), thereby obtaining the title compound (23.7 mg, 47%) as an oily colorless and transparent substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.2 Hz), 7.56 (1H, s), 7.52 (1H, td, J=8.0, 1.2 Hz), 7.24-7.24 (1H, m), 7.22-7.15 (3H, m), 7.13-7.12 (1H, m), 4.72 (1H, t, J=7.6 Hz), 4.58-4.57 (1H, d, J=14.0 Hz), 4.05-3.98 (2H, m), 3.94-3.88 (2H, m), 3.81-3.79 (1H, m), 3.74-3.71 (1H, m), 3.61 (3H, s), 3.42-3.35 (1H,), 3.01-2.92 (2H, m), 2.36 (3H, s), 1.74-1.63 (1H, m), 1.70 (3H, s), 1.53-1.38 (1H, m), 1.09 (3H, t, J=7.6 Hz).
TEA (70 μL, 0.5 mmol) was added to a 1,4-dioxane/water (2/1) (0.5 mL) solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (62.6 mg, 0.1 mmol), methyl (E)-3-[4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiazol-2-yl]acrylate (13.7 mg, 0.05 mmol), and [RhCl(cod)]2 (6.3 mg, 0.01 mmol), and the mixture was heated under microwave irradiation at 50° C. for 4 hours. The reaction solution was returned to room temperature, diluted with ethyl acetate, washed with water and saturated saline, and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=68/32→47/53), thereby obtaining the title compound (32.8 mg, quant.) as an oily colorless and transparent substance.
1H NMR (400 MHz, CDCl3) δ 7.90 (1H, d, J=7.6 Hz), 7.52 (1H t, J=7.2 Hz), 7.28-7.20 (3H, m), 7.17-7.14 (2H, m), 4.68-4.63 (1H, m), 4.58 (1H, d, J=14.0 Hz) 4.06-3.94 (3H, m), 3.88-3.79 (3H, m), 3.76-3.70 (1H, m), 3.60 (3H, s), 3.35 (1H, dt, J=16.0, 6.0 Hz), 3.00-2.93 (2H, m), 2.41 (3H, s), 2.36 (3H, s), 1.74-1.66 (4H, m), 1.51-1.45 (1H, m), 1.09 (3H, t, J=7.2 Hz).
TEA (100 μL, 0.7 mmol) was added to a 1,4-dioxane/water (2/1) (0.7 mL) solution of (R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (64.6 mg, 0.1 mmol), methyl (E)-3-(oxo-5,6-dihydro-4H-thieno[2,3-c]pyrrol-2-yl)acrylate (16.2 mg, 0.07 mmol), and [RhCl(cod)]2 (7.6 mg, 0.02 mmol), and the mixture was heated under microwave irradiation at 50° C. for 3 hours. The reaction solution was cooled to room temperature, then diluted with ethyl acetate, and washed with water and saturated saline. The obtained organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→0/100), thereby obtaining the title compound (20.1 mg, 50%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.27-7.18 (2H, m), 7.16 (2H, s), 7.11 (1H, d, J=3.6 Hz), 6.80 (1H, s), 6.47 (1H, s), 4.75 (1H, t, J=8.0 Hz), 4.56 (1H, d, J=14.4 Hz), 4.28 (2H, s), 4.04-3.97 (1H, m), 3.83-3.81 (1H, m), 3.75-3.68 (1H, m), 3.62 (3H, s), 3.12 (1H, dd, J=15.6, 8.0 Hz), 3.03 (1H, dd, J=15.6, 8.0 Hz), 2.96-2.94 (1H, m), 2.33 (3H, s), 1.73-1.64 (1H, m), 1.47-1.39 (1H, m), 1.07-1.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (120 mg, 0.3 mmol), methyl (E)-3-(5-acetylfuran-2-yl)acrylate (60.2 mg, 0.3 mmol), [RhCl(cod)]2 (6.4 mg, 0.01 mmol), 1,4-dioxane/water (3/1) (0.4 mL), and TEA (109 μL, 0.8 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (29.9 mg, 22%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, td, J=7.6, 1.6 Hz), 7.25 (1H, td, J=7.6, 1.2 Hz), 7.20 (1H, d, J=8.4 Hz), 7.16-7.11 (3H, m), 7.07 (1H, d, J=3.6 Hz), 6.16 (1H, t, J=3.6 Hz), 4.59-4.52 (2H, m), 4.05-3.99 (1H, m), 3.83-3.81 (1H, m), 3.76-3.69 (1H, m), 3.62 (3H, s), 3.17-3.11 (1H, m), 3.00-2.88 (2H, m), 2.40 (3H, s), 2.32 (3H, br s), 1.74-1.66 (1H, m), 1.50-1.41 (1H, m), 1.08-1.07 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (150 mg, 0.33 mmol), methyl (E)-3-(5-acetylthiophen-3-yl)acrylate (102.5 mg, 0.39 mmol), [RhCl(cod)]2 (8.1 mg, 0.016 mmol), 1,4-dioxane/water (3/1) (0.7 mL), and TEA (138 μL, 0.98 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (52.0 mg, 29%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.45 (1H, dd, J=3.2, 1.2 Hz), 7.29 (1H, br s), 7.24 (1H, td, J=8.0, 1.2 Hz), 7.20 (1H, br d, J=8.0 Hz), 7.14-7.12 (1H, m), 7.09-7.06 (2H, m), 4.55-4.51 (2H, m), 4.03-3.96 (1H, m), 3.84-3.66 (2H, m), 3.60 (3H, s), 3.06-3.00 (1H, m), 2.98-2.90 (2H, m), 2.48 (3H, s), 2.31 (3H, br s), 1.72-1.62 (1H, m), 1.46-1.37 (1H, m), 1.06 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (150 mg, 0.33 mmol), methyl (E)-3-(4-acetylthiophen-2-yl)acrylate (102.5 mg, 0.39 mmol), [RhCl(cod)]2 (8.1 mg, 0.016 mmol), 1,4-dioxane/water (3/1) (0.7 mL), and TEA (138 μL, 0.98 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (25.5 mg, 14%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.84 (1H, d, J=1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.27-7.19 (3H, m), 7.16-7.11 (2H, m), 7.05 (1H, d, J=10.4 Hz), 4.66 (1H, t, J=7.6 Hz), 4.57-4.56 (1H, m), 4.00-3.97 (1H, m), 3.82-3.68 (2H, m), 3.61 (3H, s), 3.10 (1H, dd, J=15.6, 7.6 Hz), 3.01-2.99 (2H, m), 2.46 (3H, s), 2.35 (3H, br s), 1.72-1.62 (1H, m), 1.48-1.36 (1H, m), 1.06 (3H, t, J=7.6 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (150 mg, 0.33 mmol), methyl (E)-3-(5-cyano-1-methyl-1H-pyrrol-3-yl)acrylate (74 mg, 0.39 mmol), [RhCl(cod)]2 (8.1 mg, 0.016 mmol), 1,4-dioxane/water (3/1) (0.7 mL), and TEA (138 μL, 0.98 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (52.4 mg, 30%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, td, J=8.0, 1.2 Hz), 7.21 (1H, d, J=8.0 Hz), 7.12 (1H, d, J=8.0 Hz), 7.08-7.04 (2H, m), 6.56-6.53 (2H, m), 4.54-4.53 (1H, m), 4.33 (1H, t, J=8.0 Hz), 4.05-3.98 (1H, m), 3.86-3.69 (2H, m), 3.68 (3H, s), 3.60 (3H, s), 2.99-2.79 (3H, m), 2.32 (3H, s), 1.75-1.66 (1H, m), 1.51-1.39 (1H, m), 1.09-1.08 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (110 mg, 0.2 mmol), methyl (E)-3-(3-acetylthiophen-2-yl)acrylate (61 mg, 0.3 mmol), [RhCl(cod)]2 (5.9 ng, 0.01 mmol), 1,4-dioxane/water (9/1) (0.6 mL), and TEA (101 μL, 0.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (24.6 mg, 19%) as an oily pale brown substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.34 (1H, d, J=5.6 Hz), 7.27-7.20 (3H, m), 7.16-7.10 (3H, m), 5.65 (1H, dd, J=8.0, 8.0 Hz), 4.61-4.59 (1H, m), 4.04-3.99 (1H, m), 3.80-3.72 (2H, m), 3.56 (3H, s), 3.13-3.07 (1H, m), 3.02-2.90 (2H, m), 2.49 (3H, s), 2.35 (3H, br s), 1.71-1.59 (1H, m), 1.51-1.42 (1H, m), 1.13-1.06 (3H, m).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (115 mg, 0.25 mmol), methyl (E)-3-[5-(2-methyl-1,3-dioxolan-2-yl)furan-2-yl]acrylate (60 mg, 0.25 mmol), [RhCl(cod)]2 (6.2 mg, 0.013 mmol), 1,4-dioxane/water (9/1) (0.4 mL), and TEA (106 μL, 0.76 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (13.5 mg, 9%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, t, J=8.0 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.13-7.12 (2H, m), 7.06 (1H, s), 6.17 (1H, d, J=3.2 Hz), 5.85 (1H, d, J=3.2 Hz), 4.56 (1H, d, J=14.0 Hz), 4.48 (1H, t, J=8.0 Hz), 4.04-3.93 (5H, m), 3.81-3.69 (2H, m), 3.60 (3H, s), 3.07 (1H, d, J=15.2, 7.2 Hz), 2.97 (1H, d, J=15.2 Hz), 2.88-2.80 (1H, m), 2.34 (3H, s), 1.75-1.65 (4H, m), 1.50-1.43 (1H, m), 1.08 (3H, t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (165 mg, 0.36 mmol), methyl (E)-3-[4-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]acrylate (137 mg, 0.54 mmol), [RhCl(cod)]2 (8.9 mg, 0.018 mmol), 1,4-dioxane/water (10/1) (0.77 mL), and TEA (151 μL, 1.08 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining the title compound (83.4 mg, 40%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, br t, J=8.0 Hz), 7.20 (1H, br d, J=8.0 Hz), 7.15-7.14 (2H, m), 7.07 (2H, br s), 6.77 (1H, dt, J=4.8, 1.2 Hz), 4.64-4.62 (1H, m), 4.58-4.57 (1H, m), 4.03-3.96 (3H, m), 3.89-3.69 (4H, m), 3.59 (3H, s), 3.08 (1H, dd, J=15.6, 6.8 Hz), 3.00-2.93 (2H, m), 2.35 (3H, br s), 1.73-1.70 (1H, m), 1.62 (3H, s), 1.45-1.41 (1H, m), 1.09-1.07 (3H, m).
A 1M LDA THF/hexane (150 μL, 0.15 mmol) solution was added under argon atmosphere at −78° C. to a THF (0.6 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (49.5 mg, 0.085 mmol). The reaction mixture was stirred at −78° C. for 30 minutes, and stirred at −40° C. for 20 minutes. Iodomethane (106 μL, 1.7 μmol) was added, and the mixture was heated to room temperature and stirred for 3 hours. Water was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=9/1→7/3), thereby obtaining the title compound (40.1 mg, 79%) as an oily colorless substance. The title compound could be separated into two isomer mixtures; isomer 1 with a shorter retention time and isomer 2 with a longer retention time were obtained.
Isomer 1: 1H NMR (400 MHz, CDCl3) δ 7.90 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, br t, J=8.0 Hz), 7.22 (1H, dd, J=8.0, 1.6 Hz), 7.14 (2H, br s), 7.06 (1H, d, J=11.2 Hz), 6.77 (1H, dd, J=3.6, 0.8 Hz), 6.69 (1H, br d, J=3.6 Hz), 4.60-4.57 (1H, m), 4.28-4.25 (1H, m), 4.02-3.88 (5H, m), 3.86-3.69 (2H, m), 3.59 (3H, s), 3.19-3.13 (1H, m), 2.95 (1H, dd, J=15.2, 2.0 Hz), 2.36-2.34 (3H, m), 1.73-1.62 (4H, m), 1.46-1.38 (1H, m), 1.11-1.04 (6H, m).
Isomer 2: 1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.26 (1H, br t, J=8.0 Hz), 7.22 (1H, dd, J=8.0, 1.6 Hz), 7.20-7.17 (1H, m), 7.11-7.07 (2H, m), 6.82 (1H, d, J=3.6 Hz), 6.73 (1H, t, J=3.6 Hz), 4.57 (1H, d, J=14.0 Hz), 4.21 (1H, d, J=11.2 Hz), 4.07-3.89 (5H, m), 3.79-3.68 (2H, m), 3.43 (3H, s), 3.21-3.10 (1H, m), 2.94 (1H, dd, J=15.2, 8.8 Hz), 2.33 (3H, s), 1.73-1.65 (4H, m), 1.51-1.42 (1H, m), 1.20 (3H, d, J=6.8 Hz), 1.15-1.07 (3H, m).
A THF (200 μL) solution of diisopropylamine (30 μL, 0.21 mmol) was cooled to −78° C. and stirred for 10 minutes. A 1.6M n-butyllithium hexane solution (110 μL, 0.18 mmol) was added at −78° C., and the mixture was heated to −40° C. and then stirred for 30 minutes. The resultant was cooled again to −78° C., and a THF (400 μL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (41.5 mcg, 0.069 mmol) was added dropwise to the reaction solution. After stirring at −78° C. for 10 minutes, the resultant was heated to −40° C. and then stirred for 10 minutes. Iodomethane (90 μL, 1.4 mmol) was added to the reaction solution, and the mixture was stirred at −40° C. for 15 minutes, then heated to room temperature, and stirred for 2 hours. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane/TEA (v/v)=23/75/2), thereby obtaining the title compound (31.2 mg, 74%) as an oily brown substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, d, J=7.6 Hz), 7.53 (1H, t, J=7.6 Hz), 7.28-7.21 (2H, m), 7.18-7.04 (3H, m), 6.57-6.51 (1H, m), 4.59-4.57 (1H, m), 4.20-4.19 (1H, m), 4.07-3.94 (3H, m), 3.92-3.82 (3H, m), 3.78-3.69 (1H, m), 3.60-3.42 (3H, m), 3.16-3.08 (1H, m), 3.00-2.92 (1H, m), 2.37-2.33 (3H, m), 2.19-2.16 (3H, m), 1.74-1.62 (1H, m), 1.66-1.65 (3H, m), 1.53-1.37 (1H, m), 1.21-0.99 (6H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)furan-2-yl]propanoate (55.7 mg, 0.098 mmol), a 1M LDA THF/hexane solution (150 μL, 0.15 mmol), iodomethane (106 μL, 1.7 mmol), and THF (0.6 mL) were used as raw materials, and the same operation was performed as in Reference Example 157, thereby obtaining the title compound (40.1 mg, 79%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, br d, J=8.0 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.28-7.23 (1H, m), 7.22-7.04 (4H, m), 6.18-6.14 (1H, m), 6.01-5.92 (1H, m), 4.58-4.51 (1H, m), 4.15-4.08 (1H, m), 4.04-3.94 (5H, m), 3.85-3.71 (2H, m), 3.63-3.44 (3H, m), 3.23-3.16 (1H, m), 2.98-2.93 (1H, m), 2.35-2.31 (3H, m), 1.69-1.66 (4H, m), 1.52-1.48 (1H, m), 1.16-0.98 (6H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (83 mg, 0.14 mmol), THF (0.9 mL), a 2M LDA THF/heptane/ethylbenzene solution (92 μL, 0.18 mmol), and iodomethane (133 μL, 2.1 mmol) were used as raw materials, and the same operation was performed as in Reference Example 157, thereby obtaining the title compound (58.0 mg, 81%) as an oily colorless substance. The title compound could be separated into two isomer mixtures by purification by silica gel column chromatography; isomer 1 with a shorter retention time (17.0 mg) and isomer 2 with a longer retention time (30.7 mg) were obtained as oily colorless substances.
Isomer 1: 1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, br t, J=8.0 Hz), 7.28-7.25 (1H, m), 7.24-7.18 (2H, m), 7.11-7.08 (3H, m), 6.86 (1H, dd, J=6.0, 1.2 Hz), 4.57-4.56 (1H, m), 4.24-4.23 (1H, m), 4.03-3.99 (3H, m), 3.85-3.68 (4H, m), 3.43 (3H, s), 3.19-3.12 (1H, m), 2.96-2.91 (1H, m), 2.32 (3H, s), 1.73-1.69 (1H, m), 1.62 (3H, s), 1.51-1.44 (1H, m), 1.20-1.19 (3H, m), 1.24-1.09 (3H, m).
Isomer 2: 1H NMR (400 MHz, CDCl3) δ 7.89 (1H, br d, J=8.0 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.28-7.24 (1H, m), 7.22-7.19 (1H, m), 7.16-7.14 (2H, m), 7.09-7.07 (1H, m), 7.03 (1H, br 9), 6.83 (1H, br s), 4.60-4.57 (1H, m), 4.28-4.27 (1H, m), 4.04-3.97 (3H, m), 3.87-3.69 (4H, m), 3.58 (3H, br s), 3.19-3.12 (1H, m), 2.97-2.93 (1H, m), 2.36-2.34 (3H, m), 1.71-1.67 (1H, m), 1.62-1.61 (3H, m), 1.46-1.37 (1H, m), 1.11-1.03 (6H, m).
A 1M LDA THF solution (96 μL, 0.096 mmol) was added at −78° C. to a THF (2.0 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(methylcarbamoyl) furan-2-yl]propanoate (43 mg, 0.08 mmol). The reaction mixture was stirred at −78° C. for 20 minutes and at −40° C. for 15 minutes. Iodomethane (100 μL, 1.6 mmol) was added, and the mixture was stirred at room temperature for 3 hours. Then, the reaction was stopped with water, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=3/7→1/1), thereby obtaining the title compound (26.4 mg, 60%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.26 (1H, t, J=7.6 Hz), 7.21 (1H, d, J=7.6 Hz), 7.15-7.10 (3H, m), 6.90 (1H, d, J=3.6 Hz), 6.10 (1H, d, J=3.6 Hz), 4.56-4.52 (2H, m), 4.04-3.99 (1H, m), 3.82 (1H, d, J=14 Hz), 3.76-3.69 (1H, m), 3.61 (3H, s), 3.13-2.86 (9H, m), 2.32 (3H, s), 1.75-1.65 (1H, m), 1.52-1.42 (1H, m), 1.08 (3H, t, J=7.2 Hz).
TFA (750 μL, 9.8 mmol) was added under argon atmosphere to a dichloromethane (1 mL) solution of methyl 3-{5-[(2,4-dimethoxybenzyl)carbamoyl]thiophen-2-yl}-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (83.4 mg, 0.12 mmol), and the mixture was stirred at room temperature for 2 hours. The solvent was concentrated under reduced pressure, and the residue was neutralized with a 1N sodium hydroxide aqueous solution and extracted with methanol/dichloromethane (1/10). The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (99.4 mg, quant.) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.35 (1H, d, J=3.6 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, br d, J=8.0 Hz), 7.14 (2H, br s), 7.08 (1H, d, J=8.4 Hz), 6.81-6.79 (1H, m), 6.01 (2H, br s), 4.70 (1H, t, J=8.0 Hz), 4.57-4.55 (1H, m), 4.02-3.95 (1H, m), 3.82-3.69 (2H, m), 3.60 (3H, s), 3.09 (1H, dd, J=15.6, 7.6 Hz), 3.02-2.91 (2H, m), 2.33 (3H, s), 1.72-1.62 (1H, m), 1.46-1.38 (1H, m), 1.07-1.06 (3H, m).
A DMF (0.50 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (29.8 mg, 0.079 mmol), (R)-4-ethyl-3,4-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (27.8 mg, 0.12 mmol), potassium carbonate (33.9 mg, 0.25 mmol), and tetrabutylammonium iodide (5.7 mg, 0.015 mmol) was stirred at 70° C. for 3 hours. The reaction solution was cooled to room temperature, and ethyl acetate was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=73/27→52/48), thereby obtaining the title compound (43.1 mg, 96%) as a white solid.
1H NMR (400 Mz, CDCl3) δ 7.87 (1H, dt, J=7.6, 1.2 Hz), 7.55-7.50 (1H, m), 7.49 (1H, d, J=4.0 Hz), 7.27-7.11 (5H, m), 6.97-6.95 (1H, m), 4.69-4.67 (1H, m), 4.56-4.55 (1H, m), 4.04-3.97 (1H, m), 3.83-3.69 (2H, m), 3.60 (3H, brs), 2.97-2.90 (1H, m), 2.49-2.48 (3H, m), 2.33 (3H, s), 1.81-1.56 (1H, m), 1.51-1.35 (1H, m), 1.29 (3H, br s), 1.23/−1.21 (3H, m), 1.10-1.08 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (23.4 mg, 0.062 mmol), (R)-4-ethyl-9-fluoro-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (18.3 mg, 0.075 mmol), potassium carbonate (27.2 mg, 0.20 mol), tetrabutylammonium iodide (5.3 mg, 0.014 mmol), and DMF (1.0 mL) were used as raw materials, and the same operation was performed as in Reference Example 163, thereby obtaining the title compound (31.8 mg, 88%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.51 (1H, dd, J=4.0, 1.6 Hz), 7.44-7.39 (1H, m), 7.29-7.28 (1H, m), 7.25-7.22 (1H, m), 7.14 (1H, br d, J=8.0 Hz), 7.00-6.94 (3H, m), 4.72 (1H, s), 4.58-4.55 (1H, m), 4.50-4.43 (1H, m), 4.31-4.28 (1H, m), 3.62 (3H, s), 3.33 (1H, d, J=14.4, 4.0 Hz), 3.10 (1H, d, J=14.4, 1.2 Hz), 2.49 (3H, br s), 2.34 (3H, br s), 1.68-1.56 (1H, m), 1.55-1.45 (1H, m), 1.32 (3H, br s), 1.25 (3H, s), 1.02-1.01 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (50 mg, 0.139 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepine 1,1-dioxide (38.1 mg, 0.167 mmol), triphenylphosphine (73 mg, 0.278 mmol), THF (0.4 mL), and a 2.2M DEAD toluene solution (126 μL, 0.278 mmol) were used as raw materials, and the same operation was performed as in Reference Example 12, thereby obtaining the title compound (39.4 mg, 50%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 8.51-8.49 (1H, m), 8.26 (1H, br d, J=8.0 Hz), 7.51 (1H, d, J=4.0 Hz), 7.30-7.24 (2H, m), 7.21 (1H, s), 7.14 (1H, d, J=8.0 Hz), 6.98 (1H, t, J=4.0 Hz), 4.69 (1H, d, J=5.6 Hz), 4.47-4.42 (2H, m), 4.11-4.05 (1H, m), 3.62-3.59 (4H, m), 3.16 (1H, br d, J=15.2 Hz), 2.50 (3H, s), 2.33 (3H, br s), 1.81-1.68 (1H, m), 1.60-1.52 (1H, m), 1.30 (3H, s), 1.24 (3H, s), 1.09 (3H, t, J=7.2 Hz).
Methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (22 mg, 0.064 mmol), 4-[2-(benzyloxy)ethyl]-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (23 mg, 0.070 mmol), triphenylphosphine (20.1 mg, 0.077 mmol), THF (0.27 mL), and a 2.2M DEAD toluene solution (38 μL, 0.083 mmol) were used as raw materials, and the same operation was performed as in Reference Example 12, thereby obtaining the title compound (29.6 mg, 70) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=8.0 Hz), 7.49 (1H, br t, J=8.0 Hz), 7.43 (1H, t, J=4.0 Hz), 7.35-7.24 (6H, m), 7.14-7.09 (3H, m), 7.00 (1H, br t, J=8.0 Hz), 6.89 (1H, br t, J=4.0 Hz), 4.60-4.47 (3H, m), 4.36-4.31 (2H, m), 3.87-3.73 (3H, m), 3.66-3.61 (1H, m), 3.59 (3H, br s), 3.25-3.18 (1H, m), 2.93-2.88 (1H, m), 2.43 (3H, br s), 2.31 (3H, br s), 1.92-1.83 (1H, m), 1.67-1.60 (1H, m), 1.06 (3H, d, J=7.2 Hz).
Methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2-methylpropanoate (50 mg, 0.14 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (38.1 mg, 0.17 mmol), triphenylphosphine (43.7 mg, 0.17 mmol), THF (3.7 mL), and a 2.2M DEAD toluene solution (100 μL, 0.22 mmol) were used as raw materials, and the same operation was performed as in Reference Example 12, thereby obtaining the title compound (24.8 mg, 31%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 9.03 (1H, s), 8.66 (1H, dd, J=5.6, 2.0 Hz), 7.47 (1H, dd, J=4.0, 2.4 Hz), 7.17 (2H, s), 7.12-7.09 (2H, m), 6.93-6.92 (1H, m), 4.47-4.44 (1H, m), 4.38 (2H, d, J=12.0 Hz), 4.21-4.09 (1H, m), 3.61 (3H, s), 3.51-3.41 (1H, m), 3.23-3.11 (2H, m), 2.47 (3H, br s), 2.33 (3H, s), 1.74-1.63 (1H, m), 1.56-1.47 (1H, m), 1.08-1.02 (6H, m).
Palladium carbon (35.7 mg) was added to a methanol/dichloromethane (0.6 mL/0.4 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-({4-[2-(benzyloxy)ethyl]-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl}methyl)-4-methylphenyl]-2-methylpropanoate (126 mg, 0.19 mmol), and the mixture was stirred at room temperature for 32 hours. The mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=1/1→0/1), thereby obtaining the title compound (44.4 mg, 41%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.69-7.44 (3H, m), 7.29-7.22 (1H, m), 7.17-7.10 (3H, m), 6.93 (1H, d, J=4.0 Hz), 4.77-4.59 (1H, m), 4.44-4.33 (2H, m), 4.02-3.80 (4H, m), 3.60-3.55 (3H, m), 3.31-3.09 (1H, m), 2.92-2.81 (1H, m), 2.49-2.34 (6H, m), 1.96-1.77 (1H, m), 1.62-1.45 (1H, m), 1.07-1.00 (3H, m).
A 2M n-butyllithium cyclohexane solution (354 μL, 0.71 mmol) was added at −78° C. to a THF (2.0 mL) solution of [1-(5-bromo-3-fluorothiophen-2-yl)ethoxy](tert-butyl)dimethylsilane (200 mg, 0.59 mmol). The mixture was stirred at −78° C. for 30 minutes, and a THF (1.5 mL) solution of 3-{[(4-methoxybenzyl)oxy]methyl}-4-methylbenzaldehyde (135.1 ng, 0.50 mmol) was added. The reaction mixture was stirred at −78° C. for 1.5 hours, and heated to room temperature. After the mixture was stirred for 1.5 hours, a saturated ammonium chloride aqueous solution was added to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=1/0→95/5), thereby obtaining the title compound (168.3 mg, 63%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.31 (1H, br s), 7.22-7.16 (3H, m), 7.10 (1H, d, J=7.6 Hz), 6.82 (2H, br d, J=8.8 Hz), 6.40 (1H, d, J=20.8 Hz), 5.76 (1H, br s), 5.09 (1H, q, J=6.4 Hz), 4.44-4.43 (4H, m), 3.74 (3H, s), 2.32 (1H, br s), 2.25 (3H, s), 1.39-1.38 (3H, m), 0.82 (9H, br s), 0.01 (3H, br s), −0.05 (3H, br s).
Trichloroacetonitrile (80 μL, 0.79 mmol) and DBU (3 μL, 0.020 mmol) were added to an acetonitrile (4.8 mL) solution of (5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)(3-{[(4-methoxybenzyl)oxy)]methyl}-4-methylphenyl)methanol (210 mg, 0.40 mmol). The mixture was stirred at room temperature for 45 minutes, and an acetonitrile (111 μL) solution of dimethylketene methyl trimethylsilyl acetal (201 μL, 0.99 mmol) and bis-(trifluoromethanesulfonyl)imide (11.1 mg, 0.040 mmol) was added and stirred at room temperature for 3.5 hours. A saturated potassium carbonate aqueous solution was added to the mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=1/0→85/15), thereby obtaining the title compound (184.3 mg, 76%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.25-7.22 (3H, m), 7.13 (1H, br t, J=8.0 Hz), 7.04 (1H, dd, J=8.0, 3.2 Hz), 6.84 (2H, br d, J=8.8 Hz), 6.55 (1H, d, J=19.6 Hz), 5.07 (1H, q, J=6.4 Hz), 4.45-4.41 (5H, m), 3.77 (3H, s), 3.54 (3H, s), 2.23 (3H, s), 1.39-1.36 (3H, m), 1.24 (3H, s), 1.15 (3H, s), 0.82 (9H, br s), 0.001 (3H, br s), −0.07 (3H, br s).
Methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (204 mg, 0.33 mmol), dichloromethane (2.9 mL), water (290 μL), and DDQ (82.6 mg, 0.36 mmol) were used as raw materials, and the same operation was performed as in Reference Example 25, thereby obtaining the title compound (109.3 mg, 66%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ7.31 (1H, s), 7.18 (1H, br t, J=8.0 Hz), 7.10 (1H, dd, J=8.0, 4.0 Hz), 6.60 (1H, d, J=19.6 Hz), 5.12 (1H, q, J=6.4 Hz), 4.67 (2H, br s), 4.50-4.47 (1H, m), 3.60 (3H, s), 2.31 (3H, s), 2.32 (3H, s), 1.59 (1H, br s), 1.43-1.42 (3H, m), 1.29 (3H, s), 1.20 (3H, br s), 0.87 (9H, br s), 0.054-0.051 (3H, m), 0.00-0.015 (3H, m).
Methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (65 mg, 0.13 mmol), (R)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (33 mg, 0.15 mmol), triphenylphosphine (38 mg, 0.15 mmol), THF (0.4 mL), and a 2.2M DEAD toluene solution (78 μL, 0.17 mmol) were used as raw materials, and the same operation was performed as in Reference Example 12, thereby obtaining the title compound (66.2 mg, 71%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.84 (1H, d, J=8.0 Hz), 7.47 (1H, br t, J=8.0 Hz), 7.23-7.13 (3H, m), 7.11-7.07 (2H, m), 6.57-6.50 (1H, m), 5.09-5.06 (1H, m), 4.52-4.49 (1H, m), 4.42-4.38 (1H, m), 3.99-3.95 (1H, m), 3.80-3.65 (2H, m), 3.55 (3H, br s), 2.95-2.89 (1H, m), 2.29 (3H, br s), 1.69-1.59 (1H, m), 1.39-1.36 (4H, m), 1.22-1.21 (3H, m), 1.14-1.13 (3H, m), 1.06-1.02 (3H, m), 0.82-0.79 (9H, m), 0.004-−0.009 (3H, m), −0.052-−0.091 (3H, m).
A 4N sodium hydroxide aqueous solution (310 μL, 1.2 mmol) was added to a methanol/1,4-dioxane (0.5 mL/0.5 mL) solution of methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (87.2 mg, 0.12 mmol), and the mixture was stirred under microwave irradiation at 100° C. for 1 hour. 1N hydrochloric acid was added to the mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (90.7 mg, quant.) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=8.0 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.27-7.20 (4H, m), 7.13-7.11 (1H, m), 6.69-6.64 (1H, m), 5.13 (1H, q, J=6.4 Hz), 4.58-4.48 (2H, m), 4.02-4.00 (1H, m), 3.86-3.73 (2H, m), 3.01-2.96 (1H, m), 2.32 (3H, s), 1.73-1.60 (1H, m), 1.52-1.48 (3H, m), 1.45-1.41 (1H, m), 1.29 (3H, s), 1.18 (3H, s), 1.10-1.06 (3H, m).
A 1N tetrabutylammonium fluoride THF solution (188 μL, 0.19 mmol) was added to a THF (0.2 mL) solution of methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (66 mg, 0.094 mmol), and the mixture was stirred at roam temperature for 2 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the mixture, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (62.1 mg, quant.) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.27-7.17 (4H, m), 7.12 (1H, d, J=7.6 Hz), 6.63-6.61 (1H, m), 5.15 (1H, q, J=6.4 Hz), 4.54-4.50 (1H, m), 4.48 (1H, br s), 4.05-4.01 (1H, m), 3.83 (1H, d, J=14.0 Hz), 3.76-3.70 (1H, m), 3.62 (3H, br s), 3.39-3.35 (1H, m), 3.00-2.95 (1H, m), 2.33 (3H, s), 1.72-1.66 (1H, m), 1.52-1.50 (3H, m), 1.48-1.42 (1H, m), 1.28 (3H, s), 1.19 (3H, br 9), 1.09 (3H, t, J=7.2 Hz).
TEA (47 μL, 0.34 mmol) and a pyridine-sulfur trioxide complex (32.9 mg, 0.21 mmol) were added to a DMSO (0.4 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-fluoro-5-(1-hydroxyethyl)thiophen-2-yl]-2,2-dimethylpropanoate (62.1 mg, 0.094 mmol). The reaction mixture was stirred at room temperature for 20 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (48.1 mg, 87%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dt, J=8.0, 1.6 Hz), 7.53 (1H, br t, J=8.0 Hz), 7.29-7.14 (5H, m), 6.75 (1H, br d, J=6.8 Hz), 4.57-4.54 (2H, m), 4.06-4.00 (1H, m), 3.85-3.82 (1H, m), 3.77-3.71 (1H, m), 3.64 (3H, br s), 3.00-2.93 (1H, m), 2.51 (3H, br s), 2.34 (3H, s), 1.71-1.65 (1H, m), 1.50-1.38 (1H, m), 1.30 (3H, s), 1.20 (3H, s), 1.09-1.08 (3H, m).
(R)-4-ethyl-2-{[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-trityl-1H-benzo[d]imidazol-4-yl]methyl}-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (126.9 mg, 0.17 mmol), methyl (E)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl)]acrylate (88.4 mg, 0.35 mmol), and [RhCl(cod)]2 (9.3 mg, 0.019 mmol) were added to a flask, and argon replacement was carried out. Then, 1,4-dioxane/water (1/1) (0.8 mL) and TEA (75 μL, 0.54 mmol) were added, and the mixture was heated under microwave irradiation at 140° C. for 3 hours. The reaction solution was returned to room temperature, diluted with ethyl acetate, washed with water and saturated saline, and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=71/29→1/1), thereby obtaining the title compound (86.6 mg, 58) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, d, J=7.6 Hz), 7.78 (1H, s), 7.47-7.42 (1H, m), 7.31-7.26 (9H, m), 7.22-7.18 (1H, m), 7.15-7.11 (8H, m), 6.70 (1H, d, J=2.0 Hz), 6.29-6.26 (2H, m), 4.77 (1H, d, J=15.2 Hz), 4.55-4.54 (1H, m), 4.48 (1H, q, J=7.2 Hz), 4.03-3.84 (6H, m), 3.53 (3H, s), 3.29-3.23 (1H, m), 2.76-2.69 (1H, m), 2.59-2.51 (1H, m), 1.73-1.64 (1H, m), 1.68 (3H, s), 1.45-1.40 (1H, m), 1.03-1.02 (3H, m).
Triethylsilane (0.1 mL) and TFA (1.0 mL) were added to a dichloromethane (0.9 mL) solution of methyl 3-(4-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-1-trityl-1H-benzo[d]imidazol-6-yl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (49.8 mg, 0.058 mmol), and the mixture was stirred at room temperature for 30 minutes. The reaction solution was adjusted to basicity with a saturated sodium hydrogen carbonate aqueous solution, extracted with ethyl acetate, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (dichloromethane/methanol=100/0→95/5) and preparative thin-layer chromatography (dichloromethane/methanol=97/3), thereby obtaining the title compound (23.2 mg, 70%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 10.6 (1H, s), 8.11 (1H, s), 7.90 (1H, dd, J=7.6, 1.2 Hz), 7.74 (1H, s), 7.56 (1H, t, J=7.6 Hz), 7.52-7.48 (1H, m), 7.31-7.24 (2H, m), 6.91 (1H, s), 6.88 (1H, br s), 4.87 (1H, t, J=7.6 Hz), 4.75-4.72 (1H, m), 4.15-4.07 (1H, m), 3.97-3.93 (1H, m), 3.74-3.71 (1H, m), 3.60 (3H, br s), 3.21-3.07 (3H, m), 2.47 (3H, s), 1.82-1.74 (1H, m), 1.59-1.51 (1H, m), 1.15-1.14 (3H, m).
1M hydrochloric acid (0.1 mL, 0.1 mmol) was added to a THF (0.5 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methyl-3-[4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (31.2 mg, 0.05 mmol), and the mixture was stirred at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate, washed with water and saturated saline, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (26.7 mg, 92%) as an oily transparent brown substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, d, J=7.6 Hz), 7.53 (1H, t, J=7.6 Hz), 7.26 (1H, t, J=7.6 Hz), 7.22 (1H, d, J=8.0 Hz), 7.17-7.07 (3H, m), 6.77-6.32 (1H, m), 4.60-4.53 (1H, m), 4.30-4.25 (1H, m), 4.06-3.98 (1H, m), 3.89-3.79 (1H, m), 3.75-3.68 (1H, m), 3.62-3.46 (3H, m), 3.24-3.14 (1H, m), 2.99-2.92 (1H, m), 2.47-2.42 (6H, m), 2.34-2.31 (3H, m), 1.73-1.62 (1H, m), 1.49-1.33 (1H, m), 1.11-1.04 (6H, m).
1M hydrochloric acid (0.1 mL) was added to a THF (0.5 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiazol-2-yl]propanoate (23.7 mg, 0.040 mmol), and the mixture was stirred for 2 hours. Further, 6M hydrochloric acid (0.1 mL) was added, and the mixture was stirred at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate, washed with water, and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (19.0 mg, 89%) an oily white substance.
1H NMR (400 MHz, CDCl3) δ 8.17 (1H, br s), 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, td, J=7.6, 1.6 Hz), 7.28-7.24 (1H, m), 7.22-7.14 (4H, m), 4.79 (1H, t, J=7.6 Hz), 4.57-4.55 (1H, m), 4.07-3.97 (1H, m), 3.84-3.81 (1H, m), 3.76-3.66 (1H, m), 3.63 (3H, s), 3.43-3.42 (1H, m), 3.02-2.96 (2H, m), 2.52 (3H, s), 2.35 (3H, br s), 1.75-1.64 (1H, m), 1.51-1.39 (1H, m), 1.09-1.07 (3H, m).
3M hydrochloric acid (0.1 mL, 0.3 mmol) was added to a THF (0.5 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-methyl-5-(2-methyl-1,3-dioxolan-2-yl)thiazol-2-yl]propanoate (32.8 mg, 0.06 mmol), and the mixture was stirred at room temperature for 5 hours. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1→dichloromethane/methanol=98/2), thereby obtaining the title compound (24.8 mg, 82%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.28-7.24 (1H, m), 7.22-7.15 (4H, m), 4.73 (1H, t, J=7.6 Hz), 4.58-4.56 (1H, m), 4.07-3.98 (1H, m), 3.85-3.82 (1H, m), 3.76-3.70 (1H, m), 3.62 (3H, s), 3.43-3.42 (1H, m), 3.01-2.94 (2H, m), 2.68 (3H, s), 2.44 (3H, s), 2.36 (3H, br s), 1.77-1.62 (1H, m), 1.52-1.38 (1H, m), 1.11-1.05 (3H, m).
A DMF (6.9 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (87.4 mg, 0.231 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (52.7 mg, 0.231 mmol), potassium carbonate (96.0 mg, 0.693 mmol), and tetrabutylammonium iodide (17.1 mg, 0.046 mmol) was stirred at room temperature for 3.5 hours. The reaction solution was cooled to room temperature, and ethyl acetate was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=67/33→46/54), thereby obtaining the title compound (181.0 mg, quant.) as an oily light yellow substance.
1H NMR (400 Mz, CDCl3) δ 9.03 (1H, s), 8.66 (1H, dd, J=5.6, 1.6 Hz), 7.51 (1H, dd, J=4.0, 1.6 Hz), 7.24-7.20 (2H, m), 7.16-7.14 (1H, m), 7.12-7.08 (1H, m), 6.98-6.96 (1H, m), 4.70/4.69 (1H, s), 4.46-4.37 (2H, m), 4.22-4.16 (1H, m), 3.60 (3H, br s). 3.53-3.44 (1H, m), 3.18-3.12 (1H, m), 2.50 (3H, br s), 2.32 (3H, br s), 1.72-1.63 (1H, m), 1.54-1.47 (1H, m), 1.30 (3H, br s), 1.24-1.22 (3H, m), 1.07-1.02 (3H, m).
2N hydrochloric acid (0.9 mL) was added to a tetrahydrofuran (1.8 mL) solution of methyl 3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (297.6 mg, 0.60 mmol), and the mixture was stirred at room temperature for 2 hours. The mixture was diluted with water and extracted with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (230.4 mg, 85%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.49 (1H, d, J=4.0 Hz), 7.28-7.24 (3H, m), 7.11 (2H, br s), 6.90-6.86 (3H, m), 4.74 (1H, t, J=8.0 Hz), 4.48 (2H, s), 4.47 (2H, s), 3.82 (3H, s), 3.62 (3H, s), 3.15-3.00 (2H, m), 2.48 (3H, s), 2.27 (3H, s).
DDQ (231.1 mg, 1.02 mmol) was added at 0° C. to a dichloromethane/water (10/1) (5.28 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)propanoate (230.4 mg, 0.509 mmol). The mixture was stirred at room temperature for 2 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=57/43→36/64), thereby obtaining the title compound (149.6 mg, 85%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.49 (1H, d, J=4.0 Hz), 7.29 (1H, br s), 7.10 (2H, br s), 6.87 (1H, br d, J=4.0 Hz), 4.74 (1H, t, J=8.0 Hz), 4.64 (2H, s), 3.60 (3H, s), 3.15-3.01 (2H, m), 2.46 (3H, s), 2.28 (3H, s).
DIPEA (115.7 μL, 0.68 mmol) and methanesulfonyl chloride (41.8 μL, 0.54 mmol) were added to a dichlormethane (3.5 mL) suspension of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]propanoate (150.0 mg, 0.45 mmol) and lithium chloride (38.4 mg, 0.91 mmol), and the mixture was stirred at roan temperature for 19 hours. Dichloromethane was added to the reaction solution, followed by washing with a saturated sodium hydrogen carbonate aqueous solution and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=67/33→46/54), thereby obtaining the title compound (105.0 mg, 67%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.51 (1H, d, J=4.0 Hz), 7.21 (1H, br s), 7.15 (2H, br s), 6.87 (1H, br d, J=4.0 Hz), 4.74 (1H, t, J=8.0 Hz), 4.56 (2H, s), 3.62 (3H, s), 3.15-3.00 (2H, m), 2.48 (3H, s), 2.38 (3H, s).
A DMF (3.0 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]propanoate (35.0 mg, 0.10 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (23.0 mg, 0.10 mmol), potassium carbonate (41.5 mg, 0.30 mmol), and tetrabutylammonium iodide (7.4 mg, 0.02 mmol) was stirred at room temperature for 4 hours. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=55/45→36/64), thereby obtaining the title compound (48.2 mg, 89%) as an oily colorless substance.
1H NMR (400 Mz, CDCl3) δ 9.02 (1H, s), 8.65 (1H, d, J=5.6 Hz), 7.50 (1H, br d, J=4.0 Hz), 7.17 (2H, br s), 7.11-7.08 (2H, m), 6.88 (1H, br d, J=4.0 Hz), 4.73 (1H, t, J=7.6 Hz), 4.45-4.37 (2H, m), 4.16-4.09 (1H, m), 3.62 (3H, s), 3.51-3.43 (1H, m), 3.17-3.09 (2H, m), 3.05-3.00 (1H, m), 2.49 (3H, s), 2.33 (3H, s), 1.74-1.65 (1H, m), 1.56-1.50 (1H, m), 1.04 (3H, br t, J=7.6 Hz).
A 1N tetrabutylamnonium fluoride THF solution (550 μL, 0.55 mmol) was added to a THF (2.0 mL) solution of methyl 3-(5-{1-[(tert-butyldimethylsilyl)oxy]ethyl}-4-fluorothiophen-2-yl)-3-(3-{([(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (131.8 mg, 0.21 mmol), and the mixture was stirred at roan temperature for 1.5 hours. The solvent was removed by distillation under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=76/24→55/45), thereby obtaining the title compound (95.5 mg, 94%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.29-7.27 (3H, m), 7.16 (1H, d, J=8.0 Hz), 7.10 (1H, d, J=8.0 Hz), 6.89 (2H, d, J=8.4 Hz), 6.64, 6.63 (each 0.5H, s), 5.18-5.12 (1H, m), 4.51-4.48 (5H, m), 3.82 (3H, s), 3.61 (3H, s), 2.28 (3H, s), 1.87 (1H, br s), 1.51, 1.50 (each 1.5H, d, J=6.4 Hz, thiophene β-CH3 regioisomers), 1.30 (3H, s), 1.20 (3H, s).
Manganese dioxide (822.2 mg, 9.45 mmol) was added to a dichloromethane (2.0 mL) solution of methyl 3-[4-fluoro-5-(1-hydroxyethyl)thiophen-2-yl]-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (95.5 mg, 0.19 mmol). The reaction mixture was stirred at room temperature for 2.5 hours. Further, manganese dioxide (317.7 mg, 3.65 mmol) was added, and the mixture was stirred at room temperature for 1 hour. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=86/14→65/35), thereby obtaining the title compound (92.1 mg, 97%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.29-7.27 (3H, m), 7.15 (1H, dd, J=7.6, 1.2 Hz), 7.11 (1H, d, J=7.6 Hz), 6.90 (2H, d, J=8.4 Hz), 6.75 (1H, s), 4.55 (1H, s), 4.49 (2H, s), 4.48 (2H, s), 3.82 (3H, s), 3.62 (3H, s), 2.51, 2.50 (each 1.5H, s), 2.28 (3H, s), 1.32 (3H, s), 1.21 (3H, s).
Methyl 3-[5-acetyl-4-fluorothiophen-2-yl]-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (92.1 mg, 0.18 mmol), dichloromethane (2.5 mL), water (250 μL), and DDQ (63.9 mg, 0.28 mmol) were used as raw materials, and the same operation was performed as in Reference Example 25, thereby obtaining the title compound (65.7 mg, 94%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.31 (1H, d, J=1.6 Hz), 7.15 (1H, dd, J=8.0, 1.6 Hz), 7.11 (1H, d, J=8.0 Hz), 6.75 (1H, s), 4.67 (2H, s), 4.55 (1H, s), 3.63 (3H, s), 2.50, 2.49 (each 1.5H, s, acetyl regioisomers), 2.29 (3H, s), 1.32 (3H, s), 1.20 (3H, s).
DIPEA (90 μL, 0.52 mmol) and methanesulfonyl chloride (27 μL, 0.35 mmol) were added to a dichloromethane (1.5 mL) suspension of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]propanoate (65.7 mg, 0.17 mmol) and lithium chloride (40.1 mg, 0.95 mmol), and the mixture was stirred at room temperature for 20 hours. Ethyl acetate was added to the reaction solution, followed by washing with a 10% citric acid aqueous solution, a saturated sodium hydrogen carbonate aqueous solution, and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (71.8 mg, quant.) as an oily transparent light brown substance.
1H NMR (400 MHz, CDCl3) δ 7.23 (1H, d, J=1.6 Hz), 7.21 (1H, dd, J=8.0, 1.6 Hz), 7.15 (1H, d, J=8.0 Hz), 6.76 (1H, s), 4.57 (2H, s), 4.44 (1H, s), 3.64 (3H, s), 2.514, 2.507 (each 1.5H, s), 2.39 (3H, s), 1.32 (3H, s), 1.22 (3H, s).
A DMF (1.0 mL) solution of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (0.17 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (41.0 mg, 0.18 mmol), potassium carbonate (72.3 mg, 0.52 mmol), and tetrabutylammonium iodide (13.1 mg, 0.035 mmol) was stirred at room temperature for 2 hours. The reaction solution was cooled to room temperature, and ethyl acetate was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=57/43→36/64), thereby obtaining the title compound (93.7 mg, 92%) as an oily colorless substance.
1H NMR (400 Mz, CDCl3) δ 9.02 (1H, s), 8.65 (1H, dd, J=5.6, 0.4 Hz), 7.21 (1H, dd, J=7.6, 1.6 Hz), 7.17-7.14 (2H, m), 7.09 (1H, d, J=5.6, 2.0 Hz), 6.76, 6.75 (each 0.5H, s), 4.55, 4.54 (each 0.5H, s), 4.47-4.36 (2H, m), 4.16, 4.14 (each 0.5H, d, J=14.4 Hz), 3.640, 3.639 (each 1.5H, s), 3.51-3.43 (1H, m), 3.17 (1H, dt, J=15.2, 2.8 Hz), 2.51, 2.50 (each 1.5H, s), 2.33, 2.32 (each 1.5H, s), 1.74-1.63 (1H, m), 1.60-1.49 (1H, m), 1.30, 1.29 (each 1.5H, s), 1.20 (3H, s), 1.05 (3H, t, J=7.2 Hz).
Methyl 3-[5-acetyl-4-fluorothiophen-2-yl]-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (609.6 mg, 1.2 mmol), methanol/1,4-dioxane (1/1) (10.0 mL), and a 4N sodium hydroxide aqueous solution (5.0 mL, 20 mmol) were used as raw materials, and the same operation was performed as in Production Example 43, thereby obtaining the title compound (497.2 mg, 82%) as an orange solid.
1H NMR (400 MHz, CDCl3) δ 7.32 (1H, d, J=2.0 Hz), 7.27 (2H, d, J=8.8 Hz), 7.21 (1H, dd, J=8.0, 2.0 Hz), 7.10 (1H, d, J=8.0 Hz), 6.89 (2H, d, J=8.8 Hz), 6.73 (1H, s), 4.63 (1H, s), 4.48 (4H, s), 3.87 (3H, s), 3.81 (3H, s), 2.46 (3H, s), 2.27 (3H, s), 1.34 (3H, s), 1.25 (3H s).
2-(Trimethylsilyl)ethanol (520 μL, 3.0 mmol), DIPEA (430 μL, 3.0 mmol), and 4-dimethylaminopyridine (63.5 mg, 0.52 mmol) were added to a dimethylformamide (5.0 mL) solution of 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoic acid (491.7 mg, 1.0 mmol), and HBTU (568.4 mg, 1.5 mmol). After the mixture was stirred at room temperature for 22 hours, DMAP (63.1 mg, 0.52 mmol) was further added, and the mixture was stirred at room temperature for 3 hours. Further, 2-(trimethylsilyl)ethanol (280 μL, 2.0 mmol) and DMAP (119.5 mg, 1.0 mmol) were added, and the mixture was stirred at room temperature for 19.5 hours. Then, the reaction solution was diluted with hexane/ethyl acetate (1/1), and washed with 1N hydrochloric acid, a saturated sodium hydrogen carbonate aqueous solution, and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=86/14→65/35), thereby obtaining the title compound (409.4 mg, 69%) as an oily transparent yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.31-7.26 (3H, m), 7.18 (1H, dd, J=7.6, 1.6H), 7.10 (1H, d, J=7.6 Hz), 6.89 (2H, d, J=8.8 Hz), 6.71 (1H, s), 4.61 (1H, s), 4.48 (4H, s), 4.10-4.05 (2H, m), 3.89 (3H, s), 3.81 (3H, s), 2.46, (3H, s), 2.27 (3H, s), 1.32 (3H, s), 1.21 (3H, s), 0.89-0.86 (2H, m), 0.01 (9H, s).
2-(Trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{([(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (409.3 mg, 0.69 mmol), dichloromethane (6.0 mL), water (600 μL), and DDQ (188.4 mg, 0.83 mmol) were used as raw materials, and the same operation was performed as in Reference Example 25, thereby obtaining the title compound (316.9 mg, 97%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.32 (1H, d, J=2.0 Hz), 7.21 (1H, dd, J=8.0, 2.0 Hz), 7.11 (1H, d, J=8.0 Hz), 6.73 (1H, s), 4.67 (2H, d, J=5.6 Hz), 4.62 (1H, s), 4.10-4.06 (2H, m), 3.91 (3H, s), 2.46 (3H, s), 2.31 (3H, s), 1.56 (1H, t, J=5.6 Hz), 1.32 (3H, s), 1.22 (3H, s), 0.90-0.86 (2H, m), 0.02 (9H, s).
DIPEA (115 μL, 0.66 mmol) and methanesulfonyl chloride (34 μL, 0.44 mmol) were added to a dichloromethane (2.0 mL) suspension of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (101.8 mg, 0.22 mmol) and lithium chloride (49.6 mg, 1.2 mmol), and the mixture was stirred at room temperature for 15.5 hours. Ethyl acetate was added to the reaction solution, followed by washing with a 10% citric acid aqueous solution, a saturated sodium hydrogen carbonate aqueous solution, and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (110.3 mg, quant.) as an oily transparent light brown substance.
1H NMR (400 MHz, CDCl3) δ 7.26-7.23 (2H, m), 7.12 (1H, d, J=7.6 Hz), 6.72 (1H, s), 4.60 (1H, s), 4.56 (2H, s), 4.09-4.05 (2H, m), 3.91 (3H, s), 2.73 (3H, s), 2.46 (3H, s), 1.31 (3H, s), 1.22 (3H, s), 0.88-0.84 (2H, m), 0.10 (9H, s).
A DMF (1.0 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2,2-dimethylpropanoate (the entire amount of the compound synthesized in Reference Example 194), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (51.0 mg, 0.22 mmol), potassium carbonate (59.6 mg, 0.43 mmol), and tetrabutylammonium iodide (18.8 mg, 0.051 mmol) was stirred at 25° C. for 1 hour, and then further stirred at 40° C. for 1 hour. The reaction solution was cooled to room temperature, and hexane/ethyl acetate (1/1) was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=63/37→42/58), thereby obtaining the title compound (154.1 mg, quant.) as an oily colorless and transparent substance.
1H NMR (400 Mz, CDCl3) δ 9.01 (1H, s), 8.66, 8.65 (each 0.5H, d, J=5.6 Hz), 7.24-7.22 (2H, m), 7.14 (1H, d, J=8.0 Hz), 7.10, 7.09 (each 0.5H, d, J=5.6 Hz), 6.76, 6.75 (each 0.5H, s), 4.60, 4.59 (each 0.5H, s), 4.45-4.36 (2H, m), 4.16-4.05 (3H, m), 3.933, 3.932 (each 1.5H, s), 3.53-3.44 (1H, m), 3.18-3.11 (1H, m), 2.46 (3H, s), 2.32 (3H, s), 1.73-1.61 (1H, m), 1.58-1.46 (1H, m), 1.30 (3H, s), 1.21, 1.20 (each 1.5H, s), 1.05, 1.03 (each 1.5H, t, J=7.2 Hz), 0.90-0.86 (2H, m), 0.02, 0.01 (each 4.5H, s).
1-(5-Bromo-3-fluorothiophen-2-yl)ethan-1-one (350.0 mg, 1.57 mmol), ethylene glycol (0.957 mL, 17.3 mmol), p-TsOH·H2O (15.0 mg, 0.08 mmol), and toluene (9.7 mL) were used as raw materials, and the same operation was performed as in Reference Example 76, thereby obtaining the title compound (386.9 mg, 92%) as an oily pale dark brown substance.
1H NMR (400 MHz, CDCl3) δ 6.78 (1H, br s), 4.07-4.03 (2H, m), 4.02-3.97 (2H, m), 1.77 (3H, s).
2-(5-Bromo-3-fluorothiophen-2-yl)-2-methyl-1,3-dioxolane (150 mg, 0.56 mmol), tetrabutylammonium chloride (7.8 mg, 0.028 mmol), PdCl2(dppf)2·CH2Cl2 (45.9 mg, 0.056 mmol), DMA (0.74 mL), methyl acrylate (151 μL, 1.7 mmol), and N,N-dicyclohexylmethylamine (359 μL, 1.7 mmol) were used as raw materials, and the same operation was performed as in Reference Example 88, thereby obtaining the title compound (86.3 mg, 56%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.58 (1H, d, J=16.0 Hz), 6.93 (1H, s), 6.20 (1H, d, J=16.0 Hz), 4.10-4.03 (2H, m), 4.02-3.99 (2H, m), 3.79 (3H, s), 1.80 (3H, s).
A 2N potassium hydroxide solution (32 μL, 0.063 mmol) was added under argon atmosphere to a toluene (0.48 mL) solution of 2-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (46.7 mg, 0.13 mmol), methyl (E)-3-[4-fluoro-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]acrylate (86.3 mg, 0.32 mmol), and [RhCl(cod)]2 (6.3 mg, 0.013 mmol), and the mixture was heated at 100° C. for 1.5 hours. Water was added to the mixture, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=87/13→66/34), thereby obtaining the title compound (43.7 mg, 67%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.27 (2H, br d, J=6.8 Hz), 7.21 (1H, br s), 7.13-7.07 (2H, m), 6.89 (2H, br d, J=6.8 Hz), 6.52 (1H, br s), 4.55 (1H, t, J=8.0 Hz), 4.48 (4H, br s), 4.01-3.91 (4H, m), 3.82 (3H, s), 3.61 (3H, s), 3.06-2.92 (2H, m), 2.28 (3H, s), 1.74 (3H, s).
A 2M LDA THF/heptane/ethylbenzene solution (0.17 mL, 0.34 mmol) was added under argon atmosphere at −78° C. to a THF (2.0 mL) solution of methyl 3-[4-fluoro-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)propanoate (170 mg, 0.33 mmol). The reaction mixture was stirred at −78° C. for 30 minutes, and then stirred at −40° C. for 20 minutes. Iodomethane (0.3 mL, 4.9 mmol) was added, and the mixture was heated to room temperature and stirred for 3 hours. Water was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=8%), thereby obtaining the title compound (141.1 mg, 81%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.27 (2H, br d, J=8.8 Hz), 7.24-7.20 (1H, m), 7.13-7.06 (2H, m), 6.90 (2H, br d, J=8.8 Hz), 6.61-6.52 (1H, m), 4.49 (4H, br s), 4.17-4.14 (1H, m), 3.98-3.89 (4H, m), 3.82 (3H, s), 3.63-3.43 (3H, m), 3.19-2.92 (1H, m), 2.28-2.25 (3H, m), 1.74-1.72 (3H, m), 1.23-1.02 (3H, m).
2N hydrochloric acid (1.2 mL) was added to a tetrahydrofuran (3.5 mL) solution of methyl 3-[4-fluoro-5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate (243.2 mg, 0.46 mmol), and the mixture was stirred at room temperature for 15 hours. The mixture was neutralized with a 1N sodium hydroxide aqueous solution and extracted with dichloromethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (216.5 mg, 97%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.28 (2H, d, J=8.4 Hz), 7.24-7.21 (1H, m), 7.14-7.06 (2H, m), 6.90 (2H, d, J=8.4 Hz), 6.71-6.63 (1H, m), 4.50-4.46 (4H, m), 4.27-4.22 (1H, m), 3.82 (3H, s), 3.65 (3H, s), 3.23-3.14 (1H, m), 2.50-2.48 (3H, m), 2.27-2.25 (3H, m), 1.24-1.06 (3H, m).
DDQ (38.1 mg, 0.17 mmol) was added at 0° C. to a dichloromethane/water (10/1) (3.5 mL) solution of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate (68.5 mg, 0.14 mmol). The mixture was stirred at room temperature for 3 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=87/13→66/34), thereby obtaining the title compound (34.5 mg, 68%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.28-7.26 (1H, m), 7.15-7.04 (2H, m), 6.73-6.65 (1H, m), 4.69-4.64 (2H, m), 4.28-4.23 (1H, m), 3.65-3.48 (3H, m), 3.26-2.98 (1H, m), 2.50-2.47 (3H, m), 2.30-2.28 (3H, m), 1.80 (1H, br s), 1.25-1.07 (3H, m).
DIPEA (42.7 μL, 0.25 mmol) and methanesulfonyl chloride (78 μL, 0.17 mmol) were added to a dichloromethane (0.75 mL) suspension of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2-methylpropanoate (30.4 mg, 0.083 mmol) and lithium chloride (64.1 mg, 0.334 mmol), and the mixture was stirred at room temperature for 16 hours. Water was added to the reaction solution, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=97/3→76/24), thereby obtaining the title compound (23.0 mg, 72%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.21-7.11 (3H, m), 6.73-6.70 (1H, m), 4.57-4.55 (2H, m), 4.28-4.21 (1H, m), 3.66-3.48 (3H, m), 3.23-3.14 (1H, m), 2.51-2.48 (3H, m), 2.39-2.36 (3H, m), 1.25-1.07 (3H, m).
A DMF (1.3 mL) solution of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2-methylpropanoate (23.0 mg, 0.06 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (13.7 mg, 0.06 mmol), potassium carbonate (24.9 mg, 0.18 mmol), and tetrabutylammonium iodide (4.4 mg, 0.012 mmol) was stirred at room temperature for 3 hours. The reaction solution was cooled to room temperature, and hexane/ethyl acetate (4/6) was added, followed by washing with water and saturated saline. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=67/33→46/54), thereby obtaining the title compound (29.6 mg, 86%) as an oily light yellow substance.
1H NMR (400 Mz, CDCl3) δ 9.03 (1H, s), 8.66 (1H, br d, J=5.6 Hz), 7.20-7.08 (4H, m), 6.73-6.70 (1H, m), 4.49-4.40 (2H, m), 4.30-4.13 (2H, m), 3.66-3.40 (4H, m), 3.21-3.13 (2H, m), 2.51-2.48 (3H, m), 2.34-2.32 (3H, m), 1.75-1.65 (1H, m), 1.61-1.50 (1H, m), 1.24-1.03 (6H, m).
Methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate (216 mg, 0.45 mmol), methanol/1,4-dioxane (1/1) (3.2 mL), and a 4N sodium hydroxide aqueous solution (1.1 mL, 4.5 mmol) were used as raw materials, and the same operation was performed as in Reference Example 43, thereby obtaining the title compound (248.9 mg, quant.) as an oily dark brown substance.
1H NMR (400 MHz, CDCl3) δ 7.28-7.06 (5H, m), 6.90-6.87 (2H, m), 6.70-6.68 (1H, m), 4.49-4.44 (4H, m), 4.25-4.21 (1H, m), 3.91-3.80 (3H, m), 3.81 (3H, br s), 3.25-3.15 (1H, m), 2.44-2.42 (3H, m), 2.26-2.23 (3H, m), 1.25-1.07 (3H, m).
2-(Trimethylsilyl)ethanol (0.37 mL, 2.58 mmol), DIPEA (0.27 mL, 1.55 mmol), and 4-dimethylaminopyridine (126.1 mg, 1.03 mmol) were added to a dimethylformamide (4.7 mL) solution of 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoic acid (248.9 mg, 0.52 mmol) and HATU (294.3 mg, 0.77 mmol). After the reaction mixture was stirred at room temperature for 22 hours, water was added, followed by extraction with hexane/ethyl acetate (1/1). The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=100/0→85/15), thereby obtaining the title compound (74.7 mg, 25%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.26 (2H, br d, J=8.8 Hz), 7.21 (1H, s), 7.09 (2H, s), 6.88 (2H, br d, J=8.8 Hz), 6.67 (1H, s), 4.47 (2H, s), 4.43 (2H, s), 4.24 (1H, d, J=11.2 Hz), 4.10-4.05 (2H, m), 3.86 (3H, s), 3.80 (3H, s), 3.17-3.09 (1H, m), 2.41 (3H, s), 2.24 (3H, s), 1.04 (3H, d, J=6.8 Hz), 0.89-0.85 (2H, m), −0.00 (9H, s).
Methyl 3-[5-acetyl-4-fluorothiophen-2-yl]-3-(3-{([(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate (74.7 mg, 0.13 mol), dichloromethane (3 mL), water (0.17 mL), and DDQ (34.9 mg, 0.15 mmol) were used as raw materials, and the same operation was performed as in Reference Example 25, thereby obtaining the title compound (57.9 mg, 98%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.28 (1H, s), 7.12 (2H, br s), 6.70 (1H, s), 4.68-4.67 (2H, m), 4.27 (1H, d, J=11.2 Hz), 4.15-4.04 (2H, m), 3.90 (3H, s), 3.19-3.12 (1H, m), 2.43 (3H, s), 2.30 (3H, s), 1.74-1.71 (1H, m), 1.06 (3H, d, J=7.2 Hz), 0.91-0.87 (2H, m), 0.02 (9H, s).
DIPEA (85.7 μL, 0.50 mmol) and methanesulfonyl chloride (29.0 μL, 0.38 mmol) were added to a dichloromethane (1.1 mL) suspension of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2-methylpropanoate (57.9 mg, 0.13 mmol) and lithium chloride (26.5 mg, 0.63 mmol), and the mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction solution, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (77.1 mg, quant.) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.18 (1H, s), 7.13 (2H, br s), 6.68 (1H, s), 4.55 (2H, s), 4.25 (1H, d, J=11.2 Hz), 4.10-4.05 (2H, m), 3.88 (3H, s), 3.16-3.08 (1H, m), 2.42 (3H, s), 2.36 (3H, s), 1.04 (3H, d, J=7.2 Hz), 0.89-0.85 (2H, m), −0.00 (9H, s).
A DMF (3.4 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2-methylpropanoate (75.0 mg, 0.16 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (35.6 mg, 0.16 mmol), potassium carbonate (64.7 mg, 0.47 mmol), and tetrabutylammonium iodide (11.5 mg, 0.031 mmol) was stirred at room temperature for 7 hours. Water was added to the reaction solution, followed by extraction with hexane/ethyl acetate (1/1). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=67/33→46/54), thereby obtaining the title compound (54.2 mg, 52%) as an oily pale yellow substance.
1H NMR (400 Mz, CDCl3) δ 9.02 (1H, s), 8.67-8.65 (1H, m), 7.16-7.09 (4H, m), 6.72 (1H, s), 4.47-4.35 (2H, m), 4.29-4.08 (4H, m), 3.92 (3H, br s), 3.52-3.41 (1H, m), 3.19-3.09 (2H, m), 2.44 (3H, s), 2.33 (3H, s), 1.75-1.64 (1H, m), 1.57-1.49 (1H, m), 1.06-1.02 (6H, m), 0.92-0.87 (2H, m), 0.02 (9H, 6).
A 2N sodium hydroxide aqueous solution (220 μL, 0.44 mmol) was added to a methanol/1,4-dioxane solution (2/1) (0.6 mL) of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(methylcarbamoyl)furan-2-yl]propanoate (47.7 mg, 0.088 mmol), and the mixture was stirred at room temperature for 21 hours. 1N hydrochloric acid was added, followed by extraction with dichloromethane/methanol (10/1). The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by preparative thin-layer chromatography (methanol/dichloromethane (v/v)=1/9), thereby obtaining the title compound (27.7 mg, 60%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.85 (1H, d, J=8.0 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.27-7.20 (3H, m), 7.12-7.06 (2H, m), 6.96 (1H, d, J=3.2 Hz), 6.59 (1H, br s), 6.14-6.21 (1H, m), 4.53-4.47 (2H, m), 4.01-3.97 (1H, m), 3.87-3.73 (2H, m), 3.13-2.87 (6H, m), 2.28 (3H, br s), 1.73-1.63 (1H, m), 1.50-1.40 (1H, m), 1.07-1.06 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(pyrrolidine-1-carbonyl)furan-2-yl]propanoate (85 mg, 0.15 mmol), methanol/dichloromethane (2/1) (0.75 mL), and a 2N sodium hydroxide aqueous solution (570 μL, 1.1 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (38.3 mg, 47%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ7.87 (1H, dd, J=7.6, 1.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.27-7.19 (2H, m), 7.12-7.10 (3H, m), 6.94 (1H, d, J=3.6 Hz), 6.09 (1H, br s), 4.55-4.51 (2H, m), 4.02-3.96 (1H, m), 3.77 (1H, d, J=12.4 Hz). 3.76-3.66 (3H, m), 3.58 (1H, t, J=6.8 Hz), 3.14 (1H, dd, J=16.0, 8.0 Hz), 2.96 (1H, d, J=15.2 Hz), 2.99-2.87 (2H, m), 2.31 (3H, s), 1.96-1.91 (2H, m), 1.88-1.71 (2H, m), 1.69-1.61 (1H, m), 1.48-1.42 (1H, m), 1.06-1.05 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(isopropylcarbamoyl)furan-2-yl]propanoate (70 mg, 0.12 mmol), methanol/dichloromethane (2/1) (0.75 mL), and a 2N sodium hydroxide aqueous solution (510 μL, 1.0 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (37.8 mg, 55%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, t, J=8.0 Hz), 7.27-7.06 (5H, m), 6.95 (1H, d, J=3.6 Hz), 6.21 (1H, d, J=8.0 Hz), 6.10-6.09 (1H, m), 4.52-4.48 (2H, m), 4.22-4.14 (1H, m), 4.02-3.95 (1H, m), 3.85-3.71 (2H, m), 3.08-2.82 (3H, m), 2.30 (3H, br s), 1.72-1.62 (1H, m), 1.49-1.38 (1H, m), 1.20-1.18 (6H, m), 1.07-1.06 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(methylcarbamoyl)thiophen-2-yl]propanoate (38.4 mg, 0.069 mmol), methanol (0.7 mL) and a 4N sodium hydroxide aqueous solution (170 μL, 0.68 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (18.8 mg, 51%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.29-7.18 (3H, m), 7.12-7.06 (3H, m), 6.76-6.75 (1H, m), 6.32 (1H, br s), 4.65 (1H, t, J=8.0 Hz), 4.53-4.52 (1H, m), 3.98-3.93 (1H, m), 3.81-3.67 (2H, m), 3.10-2.90 (3H, m), 2.87 (3H, d, J=4.8 Hz), 2.30 (3H, s), 1.67-1.56 (1H, m), 1.43-1.32 (1H, m), 1.04 (3H, t, J=7.2 Hz).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-{5-[(2-methoxyethyl)carbamoyl]furan-2-yl}propanoate (11.1 mg, 0.019 mmol), methanol (0.3 mL), and a 4N sodium hydroxide aqueous solution (150 μL, 0.6 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (10.8 mg, 92%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.16-7.11 (3H, m), 6.98 (1H, d, J=3.6 Hz), 6.77 (1H, br s), 6.10-6.09 (1H, m), 4.55-4.51 (2H, m), 4.01-3.98 (1H, m), 3.86-3.70 (2H, m), 3.58-3.53 (4H, m), 3.36 (3H, s), 3.16-3.09 (1H, m), 3.01-2.89 (2H, m), 2.32 (3H, br s), 1.73-1.63 (1H, m), 1.49-1.38 (1H, m), 1.07-1.06 (3H, m).
Methyl 3-[5-(dimethylcarbamoyl)furan-2-yl]-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (26 mg, 0.047 mmol), methanol (0.3 mL), and a 4N sodium hydroxide aqueous solution (100 μL, 0.4 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (10.1 mg, 38%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, t, J=8.0 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.12 (3H, br s), 6.88 (1H, d, J=3.6 Hz), 6.08 (1H, d, J=3.6 Hz), 4.55-4.51 (2H, m), 4.03-3.98 (1H, m), 3.82 (1H, d, J=14.4 Hz), 3.75-3.68 (1H, m), 3.16-2.86 (9H, m), 2.31 (3H, s), 1.72-1.63 (1H, m), 1.49-1.40 (1H, m), 1.07-1.06 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (100 mg, 0.18 mmol), methanol/dichloromethane (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (180 μL, 0.72 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (58.9 mg, 62%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, br d, J=8.0 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.50 (1H, d, J=3.6 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, br d, J=8.0 Hz), 7.16-7.12 (2H, m), 7.08 (1H, d, J=9.2 Hz), 6.88-6.86 (1H, m), 4.68 (1H, t, J=7.6 Hz), 4.55-4.54 (1H, m), 4.02-3.95 (1H, m), 3.82-3.79 (1H, m), 3.74-3.67 (1H, m), 3.12 (1H, dd, J=16.0, 7.6 Hz), 3.03 (1H, dd, J=16.0, 8.0 Hz), 2.94-2.92 (1H, m), 2.47 (3H, s), 2.33-2.32 (3H, m), 1.70-1.60 (1H, m), 1.45-1.35 (1H, m), 1.05 (3H, t, J=7.6 Hz).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-methyl-5-(methylcarbamoyl)furan-2-yl]propanoate (45 mg, 0.081 mmol), methanol/dichloromethane (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (101 μL, 0.405 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (25.0 mg, 57%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.27-7.19 (3H, m), 7.12-7.05 (2H, m), 6.38 (1H, br s), 5.96 (1H, d, J=3.6 Hz), 4.51-4.42 (2H, m), 4.03-3.96 (1H, m), 3.88-3.71 (2H, m), 3.08-2.97 (2H, m), 2.88-2.86 (4H, m), 2.28 (6H, br s), 1.73-1.64 (1H, m), 1.51-1.38 (1H, m), 1.07-1.06 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-(5-sulfamoylthiophen-2-yl)propanoate (78.9 mg, 0.14 mmol), methanol/dichloromethane (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (136 μL, 0.55 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (47.5 mg, 62%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.82 (1H, dt, J=8.0, 1.6 Hz), 7.50 (1H, td, J=8.0, 1.6 Hz), 7.37 (1H, d, J=4.0 Hz), 7.25-7.09 (5H, m), 6.77 (1H, d, J=3.6 Hz), 5.40 (2H, br s), 4.67 (1H, t, J=8.0 Hz), 4.48 (1H, d, J=14.4 Hz), 4.00-3.95 (1H, m), 3.83-3.82 (1H, m), 3.78-3.68 (1H, m), 3.13-2.94 (3H, m), 2.27 (3H, s), 1.69-1.59 (1H, m), 1.46-1.40 (1H, m), 1.05-1.04 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-(thiophen-2-yl)propanoate (110 mg, 0.22 mmol), methanol/dichloromethane (2/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (220 μL, 0.88 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (95.6 mg, 90%) as a white solid.
1H NMR (400 MHz, CDCl3) δ7.86 (1H, dd, J=8.0, 1.6 Hz), 7.50 (1H, td, J=8.0, 1.6 Hz), 7.25-7.17 (2H, m), 7.13-7.09 (3H, m), 7.04 (1H, d, J=9.6 Hz), 6.87-6.85 (1H, m), 6.80-6.78 (1H, m), 4.65 (1H, t, J=7.6 Hz), 4.54 (1H, d, J=14.0 Hz), 3.99-3.89 (1H, m), 3.79-3.65 (2H, m), 3.09-2.93 (3H, m), 1.65-1.55 (1H, m), 1.42-1.29 (1H, m), 1.04-1.03 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[5-(methylcarbamoyl)thiophen-3-yl]propanoate (77 mg, 0.14 mmol), methanol/dichloromethane (2/1) (1.2 mL), and a 4N sodium hydroxide aqueous solution (138 μL, 0.55 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (52.4 mg, 70%) as a white solid.
1H NMR (400 MHz, CDCl3) δ7.84 (1H, dt, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.32 (1H, dd, J=6.0, 1.6 Hz), 7.26-7.19 (2H, m), 7.14-7.03 (4H, m), 6.46 (1H, br s), 4.49-4.43 (2H, m), 3.99-3.94 (1H, m), 3.83-3.82 (1H, m), 3.78-3.70 (1H, m), 3.05-2.90 (3H, m), 2.87 (3H, d, J=4.8 Hz), 2.27 (3H, s), 1.70-1.61 (1H, m), 1.46-1.37 (1H, m), 1.05 (3H, br t, J=7.2 Hz).
(R)-4-ethyl-2-[2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (274.4 mg, 0.6 mmol), methyl (E)-3-(5-((isopropylamino)methyl)furan-2-yl)acrylate (89.4 mg, 0.4 mmol), [RhCl(cod)]2 (19.8 mg, 0.04 mmol), 1,4-dioxane/water (1/1) (1.6 mL), and TEA (168 μL, 1.2 mmol) were used as raw materials, and the same operation was performed as in Reference Example 130, thereby obtaining a mixture (14.8 mg), containing the title compound, as an oily pale yellow substance. The mixture was dissolved in methanol/dichloromethane (2/1) (1.2 mL), and a 4N sodium hydroxide aqueous solution (110 μL, 0.44 mmol) was added. The reaction mixture was stirred at room temperature for 8 hours, and the solvent was distilled under reduced pressure. The residue was purified by preparative thin-layer chromatography (methanol/dichloromethane (v/v)=1/10), thereby obtaining the title compound (23.9 mg, 7%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, dd, J=7.6, 1.6 Hz), 7.51 (1H, td, J=7.6, 1.6 Hz), 7.24 (1H, t, J=7.6 Hz), 7.20 (1H, d, J=7.6 Hz), 7.13-7.07 (3H, m), 6.67 (1H, br s), 6.23 (1H, d, J=3.2 Hz), 5.93 (1H, br s), 4.53-4.46 (2H, m), 4.03-3.94 (1H, m), 3.88 (2H, s), 3.84-3.67 (2H, m), 3.12-3.05 (1H, m), 2.99-2.89 (2H, m), 2.69 (1H, d, J=14.4, 5.6 Hz), 2.29 (3H, s), 1.72-1.63 (1H, m), 1.48-1.38 (1H, m), 1.24-1.21 (6H, m), 1.07-1.06 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[3-methyl-5-(methylcarbamoyl)thiophen-2-yl]propanoate (124 mg, 0.22 mmol), methanol/dichloromethane (2/1) (1.2 mL), and a 4N sodium hydroxide aqueous solution (540 μL, 2.2 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (83.0 mg, 69%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.84 (1H, br d, J=7.6 Hz), 7.51 (1H, br t, J=7.6 Hz), 7.25-7.16 (3H, m), 7.11-7.05 (3H, m), 6.57 (1H, br t, J=4.8 Hz), 4.67 (1H, t, J=6.8 Hz), 4.51-4.50 (UH, m), 3.97-3.93 (1H, m), 3.77-3.67 (2H, m), 2.93-2.90 (3H, m), 2.85 (3H, d, J=4.8 Hz), 2.28 (3H, br s), 2.03 (3H, s), 1.67-1.55 (1H, m), 1.42-1.31 (1H, m), 1.04-1.02 (3H, m).
Ethyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-(thiazol-5-yl)propanoate (97.3 mg, 0.19 mmol), methanol/dichloromethane (1/1) (1.6 mL), and a 4N sodium hydroxide aqueous solution (236 μL, 0.95 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (52.7 mg, 57%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 8.63 (1H, s), 7.85 (1H, dt, J=8.0, 1.6 Hz), 7.62 (1H, d, J=3.6 Hz), 7.50 (1H, td, J=8.0, 1.6 Hz), 7.23 (1H, br t, J=8.0 Hz), 7.18 (1H, d, J=8.0 Hz), 7.12-7.07 (3H, m), 4.73 (1H, t, J=7.6 Hz), 4.50 (1H, d, J=14.4 Hz), 4.00-3.92 (1H, m), 3.82-3.67 (2H, m), 3.04-2.91 (3H, m), 2.29 (3H, br s), 1.68-1.60 (1H, m), 1.43-1.27 (1H, m), 1.04-1.03 (3H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-(1-methyl-4-oxo-4,5,6,7-tetrahydro-1H-indol-2-yl)propanoate (149.8 mg, 0.27 mmol), methanol/dichloromethane (1/1) (2.4 mL), and a 4N sodium hydroxide aqueous solution (338 μL, 1.35 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (67.2 mg, 45%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.84 (1H, br t, J=8.0 Hz), 7.54-7.49 (1H, m), 7.27-7.18 (2H, m), 7.11-7.09 (1H, m), 7.06-7.02 (1H, m), 6.98-6.96 (UH, m), 6.56 (1H, s), 4.52-4.50 (1H, m), 4.42 (1H, t, J=6.4 Hz), 3.99-3.94 (1H, m), 3.80-3.64 (2H, m), 3.22-3.20 (3H, m), 3.06-2.87 (2H, m), 2.77 (1H, dd, J=16.0, 6.4 Hz), 2.66-2.59 (2H, m), 2.45-2.41 (2H, m), 2.33-2.31 (3H, m), 2.10-2.09 (2H, m), 1.74-1.58 (1H, m), 1.50-1.33 (1H, m), 1.09-1.02 (3H, m).
Methyl 3-(5-acetyl-1-methyl-1H-pyrrol-2-yl)3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (129.3 mg, 0.24 mmol), methanol/dichloromethane (1/1) (2.4 mL), and a 4N sodium hydroxide aqueous solution (300 μL, 1.2 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (111.8 mg, 89%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, d, J=8.0 Hz), 7.51 (1H, t, J=8.0 Hz), 7.26-7.18 (2H, m), 7.12-7.08 (1H, m), 7.02-6.93 (3H, m), 6.15 (1H, d, J=4.0 Hz), 4.55-4.44 (2H, m), 3.99-3.90 (1H, m), 3.81-3.65 (5H, m), 3.05 (1H, dd, J=16.0, 8.0 Hz), 2.93-2.82 (2H, m), 2.39 (3H, s), 2.32-2.29 (3H, m), 1.71-1.57 (1H, m), 1.45-1.28 (1H, m), 1.07-1.02 (3H, m).
Methyl 3-(5-acetyl-3-methylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (120 mg, 0.22 mmol), methanol/dichloromethane (1/1) (2.0 mL), and a 4N sodium hydroxide aqueous solution (270 μL, 1.1 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (99.8 mg, 85%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ7.85 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.37 (1H, s), 7.27-7.18 (2H, m), 7.14-7.06 (3H, m), 4.70-4.69 (1H, m), 4.54-4.52 (1H, m), 4.00-3.93 (1H, m), 3.80-3.65 (2H, m), 3.05-2.86 (3H, m), 2.45 (3H, br s), 2.31 (3H, br s), 2.14 (3H, s), 1.71-1.56 (1H, m), 1.45-1.31 (1H, m), 1.05-1.04 (3H, m).
Methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (50 mg, 0.089 mmol), methanol/dichloromethane (1/1) (1.2 mL), and a 4N sodium hydroxide aqueous solution (110 μL, 0.45 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (22.9 mg, 47%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.85 (1H, dd, J=8.0, 4.0 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.25-7.05 (5H, m), 6.62 (1H, br s), 4.56 (1H, t, J=7.6 Hz), 4.48 (1H, d, J=14.8 Hz), 4.02-3.94 (1H, m), 3.86-3.69 (2H, m), 3.03-2.88 (3H, m), 2.47 (3H, br s), 2.28 (3H, br s), 1.71-1.62 (1H, m), 1.48-1.40 (1H, m), 1.07-1.06 (3H, m).
Methyl 3-(5-carbamoylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (65.1 mg, 0.12 mmol), methanol/dichloromethane (1/1) (1.6 mL), and a 4N sodium hydroxide aqueous solution (150 μL, 0.6 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (25.8 mg, 41%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.73 (1H, dd, J=8.0, 1.6 Hz), 7.49 (1H, td, J=8.0, 1.6 Hz), 7.41-7.40 (1H, m), 7.20 (1H, td, J=8.0, 1.2 Hz), 7.16-7.06 (3H, m), 7.01 (1H, br d, J=16.8 Hz), 6.83-6.80 (1H, m), 4.59-4.54 (1H, m), 4.49-4.47 (1H, m), 3.92-3.86 (1H, m), 3.71-3.67 (1H, m), 3.60-3.54 (1H, m), 3.02-2.82 (2H, m), 2.78-2.73 (1H, m), 2.25 (3H, br s), 1.53-1.41 (1H, m), 1.34-1.22 (1H, m), 0.95 (3H, t, J=7.2 Hz).
Methyl 3-(5-acetyl-4-methylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (77.0 mg, 0.14 mmol), methanol/dichloromethane (1/1) (1.6 mL), and a 4N sodium hydroxide aqueous solution (175 μL, 0.7 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (47.6 mg, 63%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.89-7.85 (1H, m), 7.54-7.49 (1H, m), 7.27-6.95 (5H, m), 6.69 (1H, br s), 4.62 (1H, t, J=7.6 Hz), 4.55 (1H, d, J=14.0 Hz), 4.03-3.98 (1H, m), 3.84-3.68 (2H, m), 3.11 (1H, dd, J=16.4, 7.2 Hz), 3.04-2.87 (2H, m), 2.45 (3H, s), 2.42 (3H, s), 2.33 (3H, s), 1.70-1.61 (1H, m), 1.45-1.35 (1H, m), 1.07-1.03 (3H, m).
Methyl 3-(4-acetyl-1,3,5-trimethyl-1H-pyrrol-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (20 mg, 0.035 mml), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (42.5 μL, 0.17 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (11.5 mg, 60%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88-7.84 (1H, m), 7.52 (1H, br t, J=8.0 Hz), 7.25 (1H, br t, J=8.0 Hz), 7.20 (1H, dd, J=8.0, 3.2 Hz), 7.14-7.11 (1H, m), 7.02-6.99 (1H, m), 6.96-6.95 (1H, m), 4.81 (1H, t, J=7.6 Hz), 4.54-4.51 (1H, m), 3.99-3.94 (1H, m), 3.80-3.69 (2H, m), 3.28-3.22 (4H, m), 2.99-2.88 (2H, m), 2.42-2.41 (6H, m), 2.34-2.32 (3H, m), 2.21 (3H, s), 1.73-1.60 (1H, m), 1.46-1.32 (1H, m), 1.06-1.04 (3H, m).
Methyl 3-(5-acetyl-1-ethyl-1H-pyrrol-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (37 mg, 0.067 mmol), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (84 μL, 0.34 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (18.9 mg, 52%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dt, J=8.0, 1.6 Hz), 7.51 (1H, t, J=8.0 Hz), 7.25 (1H, t, J=8.0 Hz), 7.20 (1H, d, J=8.0 Hz), 7.14-7.09 (3H, m), 6.71-6.70 (1H, m), 6.63-6.62 (1H, m), 4.54-4.53 (1H, m), 4.35 (1H, t, J=7.6 Hz), 4.25 (2H, q, J=7.2 Hz), 4.03-3.97 (1H, m), 3.82-3.81 (1H, m), 3.75-3.68 (1H, m), 3.01-2.85 (3H, m), 2.35 (3H, s), 2.32 (3H, s), 1.70-1.61 (1H, m), 1.45-1.36 (1H, m), 1.29 (3H, t, J=7.2 Hz), 1.05-1.04 (3H, m).
Methyl 3-[5-(cyclopropanecarbonyl)thiophen-2-yl]-3-(3-{([(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (45 mg, 0.08 mmol), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (100 μL, 0.4 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (14.8 mg, 34%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dt, J=8.0, 1.6 Hz), 7.62 (1H, d, J=3.6 Hz), 7.52 (1H, br t, J=8.0 Hz), 7.25 (1H, br t, J=8.0 Hz), 7.20 (1H, br d, J=8.0 Hz), 7.14 (2H, br s), 7.07 (1H, d, J=10.4 Hz), 6.90-6.88 (1H, m), 4.69 (1H, t, J=7.6 Hz), 4.57-4.52 (1H, m), 4.02-3.93 (1H, m), 3.83-3.74 (1H, m), 3.74-3.67 (1H, m), 3.13 (1H, dd, J=16.0, 7.6 Hz), 3.03 (UH, dd, J=16.0, 7.6 Hz), 2.93 (1H, dd, J=15.2, 10.0 Hz), 2.47-2.41 (1H, m), 2.33 (3H, br s), 1.69-1.59 (1H, m), 1.43-1.34 (1H, m), 1.20-1.16 (2H, m), 1.04 (3H, t, J=7.6 Hz), 1.00-0.95 (2H, m).
Concentrated hydrochloric acid (100 μL) was added to a THF (3.0 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methyl-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (46 mg, 0.077 mmol), and the mixture was stirred at room temperature for 7 hours. The reaction mixture was diluted with water and extracted with dichloromethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The obtained residue was dissolved in methanol/dichloromethane (1/1) (1.0 mL), a 4N sodium hydroxide aqueous solution (100 μL, 0.4 mmol) was added, and the mixture was stirred at 60° C. for 6 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with methanol/dichloromethane (1/10). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=1/4), thereby obtaining the title compound (9.6 mg, 23%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.49-7.47 (1H, m), 7.28-7.24 (1H, m), 7.21 (1H, br d, J=8.0 Hz), 7.17-7.12 (2H, m), 7.11-7.07 (1H, m), 6.96 (1H, d, J=3.6 Hz), 4.61-4.53 (1H, m), 4.34 (1H, d, J=11.2 Hz), 4.06-3.95 (1H, m), 3.89-3.78 (1H, m), 3.76-3.68 (1H, m), 3.23-3.15 (1H, m), 2.98-2.89 (1H, m), 2.46 (3H, s), 2.34-2.33 (3H, m), 1.75-1.58 (1H, m), 1.48-1.32 (1H, m), 1.11-1.05 (6H, m).
Methyl 3-(5-cyanothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (22.2 mg, 0.042 mmol), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (105 μL, 0.42 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (8.0 mg, 38%) as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.43 (1H, dd, J=3.6, 0.8 Hz), 7.27-7.20 (2H, m), 7.17-7.10 (3H, m), 6.86 (1H, br d, J=4.0 Hz), 4.70 (1H, t, J=7.6 Hz), 4.54-4.49 (1H, m), 4.04-3.97 (1H, m), 3.86-3.82 (1H, m), 3.77-3.68 (1H, m), 3.15-3.01 (2H, m), 2.97 (1H, dd, J=14.0, 5.2 Hz), 2.31 (3H, s), 1.75-1.63 (1H, m), 1.47-1.37 (1H, m), 1.11-1.05 (3H, m).
A solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (43.1 mg, 0.076 mmol) in methanol/1,4-dioxane (1/1) (2.0 mL) and a 1M potassium hydroxide aqueous solution (1.0 mL, 1.0 mmol) was heated under microwave irradiation at 100° C. for 3 hours. The reaction solution was cooled to room temperature, and the pH was adjusted to neutrality with 1M hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=45/55→23/77), thereby obtaining the title compound (15.3 mg, 36%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dt, J=7.6, 2.0 Hz), 7.55-7.51 (2H, m), 7.28-7.21 (4H, m), 7.13 (1H, d, J=7.6 Hz), 7.00 (1H, d, J=4.0 Hz), 4.72-4.70 (1H, m), 4.55 (1H, d, J=14.0 Hz), 4.05-3.96 (1H, m), 3.84-3.82 (1H, m), 3.74 (1H, dd, J=15.2, 10.8 Hz), 2.98-2.97 (1H, m), 2.50 (3H, s), 2.33 (3H, s), 1.75-1.58 (1H, m), 1.50-1.39 (1H, m), 1.32 (3H, s), 1.25 (3H, s), 1.10-1.05 (3H, m).
Methanol/1,4-dioxane (1/1) (2.0 mL) of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-9-fluoro-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (31.8 mg, 0.054 mmol), and a 1M potassium hydroxide aqueous solution (1.0 mL, 1.0 mmol) were added, and heated under microwave irradiation at 100° C. for 1.5 hours. The reaction solution was returned to room temperature, and the pH was adjusted to 6 with 1M hydrochloric acid, followed by extraction with ethyl acetate and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=73/27→48/62→2/8→0/1→CH2Cl2/MeOH=9/1), thereby obtaining the title compound (22.7 mg, 73%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.52 (1H, br s), 7.44-7.37 (1H, m), 7.37-7.34 (1H, m), 7.27-7.23 (1H, m), 7.14-7.10 (1H, m), 7.04 (1H, br t, J=4.0 Hz), 6.99-6.94 (1H, m), 6.77-6.75 (1H, m), 4.78-4.55 (1H, m), 4.75 (1H, s), 4.52-4.42 (1H, m), 4.23-4.18 (1H, m), 3.50-3.32 (1H, m), 3.15-2.84 (1H, m), 2.49 (3H, s), 2.34-2.32 (3H, m), 1.61-1.49 (2H, m), 1.33 (3H, s), 1.26 (3H, s), 1.04-0.96 (3H, m).
A 1M potassium hydroxide aqueous solution (0.5 mL, 0.5 mmol) was added to a methanol/1,4-dioxane (1/1) (1.0 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(4-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-1H-benzo[d]imidazol-6-yl)propanoate (23.2 mg, 0.041 mmol), and the mixture was heated under microwave irradiation at 100° C. for 1 hour. The reaction solution was returned to room temperature, and neutralized with 1M hydrochloric acid, followed by extraction with a dichloromethane/methanol (9/1) mixed solvent and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure. The obtained residue was washed with a dichloromethane/hexane mixed solvent, thereby obtaining the title compound (12.6 mg, 56%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 8.11 (1H, s), 7.87 (1H, s), 7.86 (1H, d, J=7.6 Hz), 7.54 (1H, t, J=7.6 Hz), 7.51 (1H, br s), 7.28-7.24 (1H, m), 7.22 (1H, d, J=8.0 Hz), 6.95 (1H, s), 6.89 (1H, br s), 4.97-4.95 (1H, m), 4.69-4.66 (1H, m), 4.08-4.00 (1H, m), 3.97-3.92 (1H, m), 3.70-3.62 (1H, m), 3.24-3.22 (1H, m), 3.14-3.11 (1H, m), 3.04-3.01 (1H, m), 2.47 (3H, s), 1.76-1.67 (1H, m), 1.57-1.47 (1H, m), 1.10-1.08 (3H, m).
A 1M potassium hydroxide aqueous solution (0.8 mL, 0.8 mmol) was added to a methanol/1,4-dioxane (1/1) (1.6 mL) solution of methyl 3-(5-acetyl-4-methylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (26.7 mg, 0.05 mmol), and the mixture was heated under microwave irradiation at 100° C. for 1.5 hours. The reaction solution was returned to room temperature, and the pH was adjusted to 3 with 1M hydrochloric acid, followed by extraction with ethyl acetate and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (dichloromethane/methanol=95/5), thereby obtaining the title compound (10.9 mg, 42%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, d, J=7.6 Hz), 7.53 (1H, d, J=7.6 Hz), 7.26 (1H, t, J=7.2 Hz), 7.21 (1H, d, J=8.0 Hz), 7.18-7.07 (3H, m), 6.78 (UH, a), 4.57-4.54 (1H, d, J=14.0 Hz), 4.29 (1H, d, J=10.8 Hz), 4.07-3.98 (1H, m), 3.83-3.82 (1H, m), 3.75-3.67 (1H, m), 3.23-3.17 (1H, m), 2.93-2.47 (1H, m), 2.44 (3H, s), 2.42 (3H, s), 2.34 (3H, br s), 1.75-1.60 (1H, m), 1.44-1.33 (1H, m), 1.11-1.04 (6H, m).
A 1M potassium hydroxide aqueous solution (0.8 mL, 0.8 mmol) was added to a methanol/1,4-dioxane (1/1) (1.6 mL) solution of methyl 3-(5-acetylthiazol-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-propanoate (19.0 mg, 0.036 mmol), and the mixture was heated under microwave irradiation at 100° C. for 1.5 hours. The reaction solution was returned to room temperature, and the pH was adjusted to 5 with 1M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (dichloromethane/methanol=100/0→95/5, hexane/ethyl acetate=1/1→0/1→dichloromethane/methanol=98/2), thereby obtaining the title compound (3.8 mg, 20%) as a light brown solid.
1H NMR (400 MHz, CDCl3) δ 8.17 (1H, s), 7.87 (1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.25-7.16 (5H, m), 4.78 (1H, br s), 4.53 (1H, d, J=14.0 Hz), 4.06-3.96 (1H, m), 3.84 (1H, t, J=13.2 Hz), 3.76-3.61 (1H, m), 3.47-3.40 (1H, m), 3.04-2.93 (2H, m), 2.50 (3H, s), 2.33 (3H, s), 1.73-1.58 (1H, m), 1.50-1.40 (1H, m), 1.08-1.06 (3H, m).
A 1M potassium hydroxide aqueous solution (0.6 mL, 0.6 mmol) was added to a methanol/1,4-dioxane (1/1) (1.2 mL) solution of methyl 3-(5-acetyl-4-methylthiazol-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-propanoate (24.8 mug, 0.05 mmol), and the mixture was stirred at 100° C. for 14 hours. The reaction solution was returned to room temperature, and the pH was adjusted to 5 with 1M hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained residue was dissolved in ethyl acetate, hexane was added, and the mixture was suspended. Then, the suspension was concentrated under reduced pressure, and hexane was added again, followed by filtration under reduced pressure, thereby obtaining the title compound (21.5 mg, 89%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, d, J=7.6 Hz), 7.51 (1H, t, J=7.6 Hz), 7.25 (1H, t, J=7.6 Hz), 7.20-7.14 (4H, m), 4.69 (1H, t, J=7.2 Hz), 4.55 (1H, d, J=14.0 Hz), 4.05-3.96 (1H, m), 3.84-3.82 (1H, m), 3.75-3.70 (1H, m), 3.44 (1H, dd, J=16.4, 7.6 Hz), 3.04-2.93 (2H, m), 2.67 (3H, s), 2.43 (3H, s), 2.34 (3H, br s), 1.72-1.62 (1H, m), 1.51-1.36 (1H, m), 1.07-1.04 (3H, m).
A 1M potassium hydroxide aqueous solution (0.4 mL, 0.4 mmol) was added to a methanol/1,4-dioxane (1/1) (1.6 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-(6-oxo-5,6-dihydro-4H-thieno[2,3-c]pyrrol-2-yl)propanoate (20.1 mg, 0.03 mmol), and the mixture was refluxed for 1.5 hours. The reaction solution was cooled to room temperature, and the pH was adjusted to 3 with 1M hydrochloric acid, followed by extraction with ethyl acetate and drying over sodium sulfate. The solvent was removed by distillation under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (dichloromethane/methanol=9/1), thereby obtaining the title compound (12.2 mg, 63%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, d, J=7.6 Hz), 7.52 (1H, t, J=7.6 Hz), 7.26-7.23 (1H, m), 7.20 (1H, d, J=8.0 Hz), 7.15-7.21 (4H, m), 6.86 (1H, s), 4.75 (1H, t, J=7.2 Hz), 4.54-4.53 (1H, m), 4.25 (2H, s), 4.03-3.96 (1H, m), 3.84-3.82 (1H, m), 3.73-3.65 (1H, m), 3.12 (1H, dd, J=16.0, 8.0 Hz), 3.03 (1H, d, J=16.0, 7.2 Hz), 2.96 (1H, d, J=14.4 Hz), 2.32 (3H, s), 1.71-1.60 (1H, m), 1.46-1.36 (1H, m), 1.05 (3H, t, J=7.2 Hz).
Methyl 3-(5-acetylfuran-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (29.9 mg, 0.057 mmol), methanol/dichloromethane (1/1) (1.2 mL), and a 4N sodium hydroxide aqueous solution (200 μL, 0.8 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (23.5 mg, 81%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.87 (1H, dd, J=8.0, 1.6 Hz), 7.51 (1H, td, J=8.0, 1.6 Hz), 7.26-7.19 (2H, m), 7.15-7.10 (3H, m), 7.06 (1H, d, J=3.6 Hz), 6.15-6.13 (1H, m), 4.56-4.50 (2H, m), 4.04-3.96 (1H, m), 3.85-3.80 (1H, m), 3.76-3.68 (1H, m), 3.18-3.12 (1H, m), 3.00-2.89 (2H, m), 2.39 (3H, s), 2.31 (3H, s), 1.70-1.64 (1H, m), 1.49-1.38 (1H, m), 1.08-1.04 (3H, m).
Methyl 3-(5-acetylthiophen-3-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (52 mg, 0.096 mmol), methanol/dichloromethane (1/1) (2.0 mL), and a 4N sodium hydroxide aqueous solution (360 μL, 0.14 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (39.2 mg, 77%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.86 (1H, d, J=8.0 Hz), 7.51 (1H, br t, J=8.0 Hz), 7.45 (1H, dd, J=4.0, 1.2 Hz), 7.29 (1H, br s), 7.26-7.18 (2H, m), 7.13-7.05 (3H, m), 4.53-4.49 (2H, m), 4.01-3.94 (1H, m), 3.84-3.79 (1H, m), 3.74-3.67 (1H, m), 3.07-2.92 (3H, m), 2.47 (3H, s), 2.29 (3H, s), 1.69-1.60 (1H, m), 1.45-1.33 (1H, m), 1.04 (3H, t, J=7.2 Hz).
Methyl 3-(4-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (25.5 mg, 0.047 mmol), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (176.5 μL, 0.7 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (10.2 mg, 40%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=8.0 Hz), 7.84 (1H, br s), 7.52 (1H, br t, J=8.0 Hz), 7.27-7.23 (2H, m), 7.21-7.18 (1H, m), 7.16-7.11 (2H, m), 7.08-7.05 (1H, m), 4.65-4.61 (1H, m), 4.55 (1H, d, J=14.0 Hz), 4.02-3.94 (1H, m), 3.83-3.68 (2H, m), 3.15-3.12 (1H, m), 3.04-2.90 (2H, m), 2.47 (3H, s), 2.29 (3H, br s), 1.69-1.60 (1H, m), 1.45-1.33 (1H, m), 1.06-1.02 (3H, m).
Methyl 3-(5-cyano-1-methyl-1H-pyrrol-3-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (52.4 mg, 0.1 mmol), methanol/dichloromethane (1/1) (1.6 mL), and a 4N sodium hydroxide aqueous solution (375 μL, 1.5 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (33.0 mg, 65%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=8.0, 1.6 Hz), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.25 (1H, td, J=8.0, 1.2 Hz), 7.21 (1H, d, J=8.0 Hz), 7.13-7.11 (1H, m), 7.08-7.06 (2H, m), 6.57-6.54 (2H, m), 4.53 (1H, d, J=14.4 Hz), 4.33-4.29 (1H, m), 4.04-3.97 (1H, m), 3.85-3.81 (1H, m), 3.75-3.70 (1H, m), 3.68 (3H, s), 2.99-2.82 (3H, m), 2.31 (3H, s), 1.73-1.64 (1H, m), 1.47-1.38 (1H, m), 1.09-1.06 (3H, m).
Methyl 3-(3-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (24.6 mg, 0.045 mmol), methanol/dichloromethane (2/1) (1.05 mL), and a 4N sodium hydroxide aqueous solution (169 μL, 0.68 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (17.3 mg, 72%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=8.0 Hz), 7.51 (1H, br t, J=8.0 Hz), 7.33 (1H, d, J=5.6 Hz), 7.27-7.19 (3H, m), 7.14-7.10 (3H, m), 5.62-5.57 (UH, m), 4.61-4.56 (1H, m), 4.02-3.96 (1H, m), 3.78-3.66 (2H, m), 3.14-3.07 (1H, m), 3.02-2.89 (2H, m), 2.48 (3H, br s), 2.35 (3H, br s), 1.69-1.56 (1H, m), 1.45-1.35 (1H, m), 1.10-1.02 (3H, m).
A 2M DEAD toluene solution (76 μL, 0.17 mmol) was added at 0° C. to a THF (0.3 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2,2-dimethylpropanoate (50 mg, 0.14 mmol), (R)-4-methyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (29.6 mg, 0.14 mmol), and triphenylphosphine (36.5 mg, 0.14 mmol). The reaction mixture was stirred at room temperature for 29 hours, and water was added, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=70/30→50/50), and the obtained oily colorless substance (35.9 mg) was dissolved in 1,4-dioxane/methanol (1/1) (1.2 mL). A 4N sodium hydroxide aqueous solution (100 μL, 0.4 mmol) was added to the solution, and the mixture was heated under microwave irradiation at 100° C. for 1.5 hours. 1N hydrochloric acid was added, followed by extraction with methanol/dichloromethane (1/9). The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=35/65), thereby obtaining the title compound (8.7 mg, 12%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=8.0 Hz), 7.55-7.50 (2H, m), 7.28-7.20 (4H, m), 7.15-7.12 (1H, m), 7.01-7.00 (1H, m), 4.71 (1H, d, J=4.8 Hz), 4.58-4.57 (1H, m), 4.35-4.26 (1H, m), 3.84-3.70 (2H, m), 2.95-2.91 (1H, m), 2.50 (3H, s), 2.34 (3H, br s), 1.34-1.31 (3H, m), 1.28-1.24 (6H, m).
Methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methyl-3-[5-(2-methyl-1,3-dioxolan-2-yl)furan-2-yl]propanoate (33.9 mg, 0.058 mmol) was dissolved in a 1,4-dioxane (300 μL, 1.2 mol) solution of 4N hydrochloric acid, and the mixture was stirred for 4 hours. The reaction mixture was diluted with water and extracted with dichloromethane. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The obtained residue was dissolved in methanol/THF (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (220 μL, 0.88 mmol) was added and stirred at room temperature for 16 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with methanol/dichlormethane (1/10). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=4/1), thereby obtaining the title compound (5.0 mg, 16%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.28-7.24 (1H, m), 7.23-7.20 (1H, m), 7.18-7.11 (3H, m), 7.06 (1H, br d, J=3.6 Hz), 6.25 (1H, d, J=3.6 Hz), 4.58-4.52 (1H, m), 4.24 (1H, d, J=10.8 Hz), 4.07-3.97 (1H, m), 3.89-3.81 (1H, m), 3.76-3.68 (1H, m), 3.22-3.16 (1H, m), 3.00-2.93 (1H, m), 2.39 (3H, s), 2.33 (3H, s), 1.74-1.63 (1H, m), 1.49-1.35 (1H, m), 1.10-1.04 (6H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (39.4 mg, 0.069 mmol), methanol/dichloromethane (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (259 μL, 1.04 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (16.7 mg, 43%) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 8.22 (1H, br t, J=8.0 Hz), 7.69-7.64 (1H, m), 7.51 (1H, t, J=3.6 Hz), 7.32-7.19 (2H, m), 7.07-7.03 (2H, m), 6.43-6.38 (1H, m), 4.66-4.38 (3H, m), 3.51-3.25 (3H, m), 2.48-2.46 (3H, m), 2.28 (3H, s), 1.33-1.24 (8H, m), 0.81-0.76 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-({4-[2-(benzyloxy)ethyl]-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl}methyl)-4-methylphenyl)-2-methylpropanoate (29.6 mg, 0.045 mmol), methanol/dichloromethane (1/1) (0.66 mL), and a 4N sodium hydroxide aqueous solution (168 μL, 0.67 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (6.7 mg, 23%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.2 Hz), 7.50-7.42 (2H, m), 7.39-7.24 (6H, m), 7.18-7.00 (3H, m), 6.96-6.77 (2H, m), 4.76-4.36 (4H, m), 4.34-4.19 (1H, m), 3.93-3.80 (2H, m), 3.77-3.74 (1H, m), 3.63-3.58 (1H, m), 3.31-3.19 (1H, m), 2.88-2.76 (1H, m), 2.47-2.44 (3H, m), 2.39-2.31 (3H, m), 2.00-1.64 (2H, m), 1.12 (3H, t, J=6.8 Hz).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[4-(2-hydroxyethyl)-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (19 mg, 0.033 mmol), methanol/dichloromethane (1/1) (1.0 mL), and a 4N sodium hydroxide aqueous solution (125 μL, 0.5 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound. The title compound could be separated into two isomer mixtures by preparative thin-layer chromatography; isomer mixture 43a with a shorter retention time (2.7 mg, 15%) was obtained as a pale yellow solid, and isomer mixture 43b with a longer retention time (2.5 mg, 14%) was obtained as a pale yellow solid.
43a: 1H NMR (400 MHz, CDCl3) δ 7.90-7.85 (1H, m), 7.55-7.40 (2H, m), 7.31-7.27 (1H, m), 7.24-7.13 (2H, m), 7.10-7.03 (2H, m), 6.92-6.82 (1H, m), 4.74-4.62 (1H, m), 4.41-4.39 (1H, m), 4.31-4.18 (1H, m), 4.04-3.77 (3H, m), 3.72-3.60 (1H, m), 3.12-3.05 (1H, m), 2.87-2.77 (1H, m), 2.49-2.29 (1H, m), 1.89-1.56 (2H, m), 1.12-0.92 (3H, m).
43b: 1H NMR (400 MHz, CDCl3) δ 7.90-7.85 (1H, m), 7.55-7.47 (1H, m), 7.42-7.32 (1H, m), 7.29-7.24 (1H, m), 7.22-7.13 (2H, m), 7.11-7.03 (2H, m), 6.93-6.84 (1H, m), 4.75-4.61 (1H, m), 4.44-4.18 (2H, m), 4.05-3.79 (3H, m), 3.73-3.60 (1H, m), 3.15-3.09 (1H, m), 2.88-2.77 (1H, m), 2.49-2.30 (6H, m), 1.91-1.77 (1H, m), 1.63-1.53 (1H, m), 1.14-0.96 (3H, m).
Methyl 3-(5-acetyl-4-fluorothiophen-2-yl)3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (48 mg, 0.082 mmol), methanol/1,4-dioxane (1/1) (0.6 mL), and a 4N sodium hydroxide aqueous solution (306 μL, 1.23 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (4.5 mg, 9%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=7.6 Hz), 7.53 (1H, br t, J=7.6 Hz), 7.28-7.20 (5H, m), 7.12 (1H, dd, J=7.6, 2.4 Hz), 6.82-6.80 (1H, m), 4.60 (1H, d, J=3.6 Hz), 4.54 (1H, d, J=14.4 Hz), 4.03-3.99 (1H, m), 3.93 (3H, s), 3.87-3.81 (1H, m), 3.78-3.71 (1H, m), 2.97 (1H, dd, J=7.6, 1.2 Hz), 2.47 (3H, br s), 2.32 (3H, s), 1.74-1.62 (1H, m), 1.49-1.37 (1H, m), 1.33 (3H, br s), 1.25 (3H, br s), 1.11-1.06 (3H, m).
2N hydrochloric acid (150 μL) was added to a THF (0.3 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methyl-3-[4-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (30 mg, 0.05 mmol), and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was neutralized with a 1N sodium hydroxide aqueous solution, and extracted with dichlormethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The obtained residue (26.5 mg) was dissolved in methanol/dichloromethane (1/1) (1.76 mL), and a 4N sodium hydroxide aqueous solution (188 μL, 0.75 mmol) was added and stirred at 60° C. for 6 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with methanol/dichloromethane (1/10). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=7/3), thereby obtaining the title compound (11.2 mg, 41%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, br d, J=7.6 Hz), 7.83 (1H, dd, J=10.4, 1.2 Hz), 7.55-7.50 (1H, m), 7.36-7.35 (1H, m), 7.28-7.25 (1H, m), 7.24-7.19 (1H, m), 7.17-7.04 (3H, m), 4.66-4.53 (1H, m), 4.30 (1H, d, J=10.8 Hz), 4.03-3.64 (3H, m), 3.31-3.02 (1H, m), 2.96-2.88 (1H, m), 2.46-2.44 (3H, m), 2.35-2.33 (3H, m), 1.70-1.60 (1H, m), 1.44-1.32 (1H, m), 1.09-1.03 (6H, s).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (24.8 mg, 0.045 mmol), methanol/THF (1/1) (0.6 mL), and a 4N sodium hydroxide aqueous solution (170 μL, 0.67 mmol) were used as raw materials, and the same operation was performed as in Reference Example 3, thereby obtaining the title compound (5.7 mg, 24%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.67-8.65 (1H, m), 7.49-7.47 (1H, m), 7.17 (2H, s), 7.12-7.10 (2H, m), 6.99-6.97 (1H, m), 4.47-4.36 (3H, m), 4.22-4.10 (1H, m), 3.50-3.40 (1H, m), 3.26-3.12 (2H, m), 2.47 (3H, s), 2.33 (3H, s), 1.74-1.63 (1H, m), 1.56-1.48 (1H, m), 1.12 (3H, d, J=6.8 Hz), 1.06-1.02 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[4-(2-methoxyethyl)-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (5.5 mg, 0.0094 mmol), methanol/THF (1/1) (0.6 mL), and a 4N sodium hydroxide aqueous solution (105 μL, 0.42 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (2.3 mg, 43%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.96-7.89 (1H, m), 7.59-7.54 (1H, m), 7.52-7.46 (1H, m), 7.37-7.27 (2H, m), 7.20-7.10 (3H, m), 6.97-6.88 (1H, m), 4.81-4.73 (1H, m), 4.64-4.43 (1H, m), 4.36-4.21 (1H, m), 3.91-3.72 (3H, m), 3.67-3.54 (1H, m), 3.49-3.41 (3H, m), 3.35-3.16 (1H, m), 2.88-2.69 (1H, m), 2.50-2.35 (6H, m), 1.89-1.74 (1H, m), 1.69-1.66 (1H, m), 1.21-1.12 (3H, m).
Manganese dioxide (647 mg, 7.4 mmol) was added to a dichloromethane (2.0 mL) solution of 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-3-[4-fluoro-5-(1-hydroxyethyl)thiophen-2-yl]-2,2-dimethylpropanoic acid (90.7 mg, 0.12 mmol), and the mixture was stirred under heating and refluxing for 2 hours. The mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=3/2), thereby obtaining the title compound (13.1 mg, 18%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dt, J=8.0, 1.6 Hz), 7.53 (1H, br t, J=8.0 Hz), 7.28-7.20 (4H, m), 7.16-7.14 (1H, m), 6.79 (1H, d, J=5.2 Hz), 4.57-4.54 (2H, m), 4.06-4.01 (1H, m), 3.86-3.84 (1H, m), 3.74 (1H, dd, J=15.2, 10.4 Hz), 2.97 (1H, dd, J=15.2, 5.6 Hz), 2.51 (3H, br s), 2.34 (3H, s), 1.74-1.61 (1H, m), 1.49-1.41 (1H, m), 1.33 (3H, s), 1.26 (3H, br s), 1.08 (3H, br t, J=7.2 Hz).
Lithium iodide (56.2 mg, 0.42 mmol) was added to a pyridine (306 μL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (40.0 mg, 0.070 mmol), and the mixture was heated to reflux at 120° C. for 48 hours. The reaction solution was cooled to room temperature, and the solvent was distilled under reduced pressure. The pH was adjusted to 4 with 1N hydrochloric acid, followed by extraction with dichloromethane. The obtained organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (methanol/ethyl acetate (v/v)=2/98), thereby obtaining the title compound (6.0 mg, 15%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.00 (1H, br s), 8.66-8.63 (1H, m), 7.54 (1H, d, J=3.6 Hz), 7.30-7.26 (2H, m), 7.16-7.10 (2H, m), 7.05-7.03 (1H, m), 4.75-4.74 (1H, m), 4.46-4.37 (2H, m), 4.17-4.11 (1H, m), 3.46-3.43 (1H, m), 3.20-3.14 (1H, m), 2.50 (3H, s), 2.32 (3H, s), 1.73-1.63 (1H, m), 1.57-1.47 (1H, m), 1.32 (3H, s), 1.27-1.26 (3H, m), 1.06-1.02 (3H, m).
Methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)propanoate (48.2 mg, 0.089 mmol), methanol/tetrahydrofuran (1/1) (0.8 mL), and a 4N sodium hydroxide aqueous solution (190 μL, 0.76 mmol) were used as raw materials, and the same operation was performed as in Production Example 1, thereby obtaining the title compound (8.6 mg, 18%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.00 (1H, s), 8.62 (1H, d, J=5.6 Hz), 7.49 (1H, br s), 7.16-7.08 (4H, m), 6.88 (1H, br s), 4.71 (1H, t, J=7.6 Hz) 4.43-4.37 (2H, m), 4.16-4.12 (1H, m), 3.51-3.42 (1H, m), 3.19-3.02 (3H, m), 2.47 (3H, s), 2.32 (3H, s), 1.70-1.61 (1H, m), 1.56-1.48 (1H, m), 1.02 (3H, t, J=7.6 Hz).
Lithium iodide (49.7 mg, 0.37 mmol) was added to a pyridine (300 μL) solution of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (35.9 mg, 0.061 mmol), and the mixture was heated to reflux at 125° C. for 18 hours. The reaction solution was cooled to room temperature, and the solvent was distilled under reduced pressure. The pH was adjusted to 5 with 1N hydrochloric acid, followed by extraction with dichloromethane. The obtained organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (dichloromethane/methanol (v/v)=95/5), thereby obtaining the title compound (10.6 mg, 30%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.00, 8.99 (each 0.5H, s), 8.65, 8.64 (each 0.5H, d, J=5.6 Hz), 7.26-7.23 (3H, m), 7.16 (1H, d, J=7.6 Hz), 7.11, 7.10 (each 0.5H, d, J=5.4 Hz), 6.84, 6.83 (each 0.5H, s), 4.59, 4.58 (each 0.5H, s), 4.51-4.43 (1H, m), 4.39, 4.38 (each 0.5H, d, J=14.4 Hz), 4.17 (1H, d, J=14.4 Hz), 3.50-3.42 (1H, m), 3.21, 3.18 (each 0.5H, dd, J=14.4, 4.8 Hz), 2.52, 2.51 (each 1.5H, s), 2.33, 2.32 (each 1.5H, s), 1.74-1.63 (1H, m), 1.61-1.50 (1H, m), 1.34, 1.33 (each 1.5H, s), 1.25 (3H, s), 1.04 (3H, t, J=7.2 Hz).
A 1M tetrabutylammonium fluoride THF solution (420 μL, 0.42 mmol) was added to a DMF (1.5 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (the entire amount of the compound synthesized in Reference Example 195), and the mixture was stirred at room temperature for 2 hours. Water was added to the mixture, and the pH was adjusted to 5 with 1M hydrochloric acid, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was removed under reduced pressure. Then, the obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v)=1/0/37→96/4), thereby obtaining the title compound (104.5 mg, 83%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.01, 9.00 (each 0.5H, s), 8.65, 8.64 (each 0.5H, d, J=5.6 Hz), 7.29-7.26 (2H, m), 7.14 (1H, d, J=7.6 Hz), 7.11, 7.10 (each 0.5H, d, J=5.6 Hz), 6.83, 6.82 (each 0.5H, s), 4.64, 4.61 (each 0.5H, s), 4.48-4.42 (1H, m), 4.37 (1H, d, J=14.4 Hz), 4.17 (1H, d, J=14.4 Hz), 3.94 (3H, s), 3.50-3.43 (1H, m), 3.22-3.15 (1H, m), 2.47 (3H, s), 2.312, 2.311 (each 1.5H, s), 1.74-1.64 (1H, m), 1.58-1.50 (1H, m), 1.344, 1.341 (each 1.5H, s), 1.28, 1.27 (each 1.5H, s), 1.05, 1.04 (each 1.5H, t, J=7.2 Hz).
Lithium iodide (66.8 mg, 0.5 mmol) was added to a pyridine (200 μL) solution of methyl 3-(5-acetyl-4-fluorothiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (28.7 mg, 0.05 mmol), and the mixture was heated under microwave irradiation at 140° C. for 2.5 hours. The reaction solution was cooled to room temperature, and the solvent was distilled under reduced pressure. The pH was adjusted to 4 with 1N hydrochloric acid, followed by extraction with dichloromethane. The obtained organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (methanol/dichloromethane (v/v)=5/95), thereby obtaining the title compound (2.0 mg, 7%) as a light yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.02-9.00 (1H, m), 8.67-8.64 (1H, m), 7.20-7.09 (4H, m), 6.76-6.74 (1H, m), 4.46-4.35 (2H, m), 4.30-4.10 (2H, m), 3.51-3.40 (1H, m), 3.22-3.15 (2H, m), 2.51-2.48 (3H, m), 2.33-2.31 (3H, m), 1.75-1.66 (1H, m), 1.58-1.52 (1H, m), 1.11 (3H, br d, J=7.2 Hz), 1.05 (3H, br t, J=7.6 Hz).
A 1M tetrabutylammonium fluoride THF solution (315 μL, 0.32 mmol) was added to a THF (0.7 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate (42.4 mg, 0.063 mmol), and the mixture was stirred at room temperature for 2 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with dichloromethane/methanol (95/5). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v)=100/0→99/1), thereby obtaining the title compound (22.5 mg, 62%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.65-8.63 (1H, m), 7.14-7.08 (4H, m), 6.73 (1H, s), 4.46-4.35 (2H, m), 4.29-4.26 (1H, m), 4.22-4.10 (1H, m), 3.87-3.86 (3H, m), 3.55-3.44 (1H, m), 3.22-3.08 (2H, m), 2.38 (3H, br s), 2.31 (3H, s), 1.73-1.65 (1H, m), 1.54-1.49 (1H, m), 1.05-1.01 (6H, m).
Compounds 1 to 53 produced in the Production Examples were used as test substances.
The inhibitory activity of each compound on the binding between NRF2 and KEAP1 was measured by bioluminescence resonance energy transfer (BRET) assay. A plasmid having human NRF2 (Original Clone ID: ha01449s1) sequence fused with NanoLuc (19 kDa, Promega) at the N-terminal was transduced into HCE-T cells (immortalized human corneal epithelial cells) using FuGENE HD (Promega). 48 hours after transduction, the cell lysate was collected and used as an NRF2-expressing cell lysate. A plasmid having human KEAP1 (Original Clone ID: cs00328) sequence fused with HaloTag (33 kDa, Promega) at the C-terminal was transduced into HCE-T cells using FuGENE HD (Promega). After 24 hours, HaloTag Nano BRET 618 Ligand (Promega) was added to the medium. The cell lysate cultured for 24 hours after the addition was used as a KEAP1-expressing cell lysate.
The NRF2-expressing cell lysate and the KEAP1-expressing cell lysate were adjusted so that the luminescence and fluorescence intensities per well were constant. Tables 1 and 2 show the formulation of each reaction solution.
Each test substance at a concentration 100 times higher than the test concentration was dissolved in dimethylsulfoxide for adjustment. 49 μL of KEAP1 solution was added to a 96-well polystyrene microplate (FALCON) to which 1 μL of each test substance solution was added, followed by incubation for 15 minutes. Then, 50 μL of NRF2 solution was added to the above solution, followed by incubation for 1 hour. To measure the binding between NRF2 and KEAP1, NanoBRET Nano-Glo Substrate (Promega) diluted with Opti-Mem (Thermo Fisher Scientific) was added, followed by shaking for 30 seconds. Then, luminescence and fluorescence were measured using the GloMax Discover System (Promega). A 495-nm short pass filter and a 600-nm long pass filter were respectively used to measure donor and acceptor emission values. A value obtained by dividing the acceptor emission value by the donor emission value was regarded as BRET value. A BRET value when the compound was not added, and a BRET value when the KEAP1 solution was not added were respectively used as binding rates of 100% and 0%, and the binding rate when the compound was added was calculated. Further, using this binding rate, the 50% binding inhibitory activity concentration (IC50) was calculated from the following formula. The test was performed at N=2.
IC50(M)=10{circumflex over ( )}(LOG(A/B)×(50−C)/(D−C)+LOG(B))
The NRF2 activating action of the compounds on cells was measured by a reporter gene assay. pGL4.37[luc2P/ARE/Hygro] (Promega) was introduced into HCE-T cells using FuGENE HD. Cells that acquired drug resistance as a result of transduction were screened by culture in the presence of 50 μg/mL hygromycin, and a clone strain, HCE-T/ARE-Luc cells, was established.
HCE-T/ARE-Luc cells were cultured using DMEM/F12 medium containing 10 ng/mL hEGF, 5 μg/mL insulin, 5% FBS, and 40 μg/mL gentamicin. As the assay medium, a medium with the same composition as that for the culture was prepared using phenol red-free DMEM/F12 medium.
HCE-T/ARE-Luc cells were seeded in a 96-well polystyrene microplate (FALCON) with 10000 cells per well. The cells were incubated in a CO2 incubator at 37° C. for 16 hours to allow for cell adhesion. The test substance was dissolved in dimethylsulfoxide to prepare a solution at a concentration 1000 times higher than the test concentration. The cells were treated with the test substance diluted 1000-fold with the assay medium and cultured for 24 hours. When measuring the activity of the reporter, the medium containing the test substance was removed, and then a new medium and a substrate of ONE-GloEX Luciferase Assay System (Promega) were added. The plate was shaken for 1 minute and then allowed to stand at ordinary temperature for 10 minutes, and luminescence was detected using the GloMax Discover System (Promega).
The test was performed at N=3, and the 50% activation concentration of each test substance was calculated by creating a calibration curve between two concentrations across the luminescence incensity of 50%.
Some of the results are shown in Tables 3 to 9. Tables 3 to 6 and 8 show IC50 (nM, binding assay) results, and Tables 7 and 9 show EC50 (nM, reporter assay) results. The structures of the compounds in Tables 3 to 9 are as follows.
The above results show that a compound represented by formula (X):
wherein R1a and R1b are identical or different and represent a hydrogen atom, an alkyl group, or a halogen atom; R4 and R5 are identical or different and represent a hydrogen atom or an optionally substituted alkyl group, or R4 and R5 bind with each other to form —NH—CH═N—; R6 represents an optionally substituted alkyl group; A1, A2, A3, and A4 are identical or different and represent CH or N wherein the number of N is 1 or less; and Z represents a hydrogen atom or a halogen atom, has Nrf2-activating action. In addition, a prodrug form (e.g., in formula (X), —COOH is replaced by —C(═O)—R7a, wherein R7a is hydrolyzable group or —NR71R72 (wherein R71 and R72 are identical or different and represent a hydrogen atom or a —[C(═O)]0-1-hydrocarbon group)) that is hydrolyzed under physiological conditions or hydrolyzed by an enzyme in the body (e.g., an esterase such as carboxylesterase in the body) to produce a compound represented by formula (X) was also considered to be useful as a prodrug of the compound represented by formula (X).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
A 2M LDA THF/heptane/ethylbenzene solution (1.83 mL, 3.67 mmol) was added under argon atmosphere at −78° C. to a THF (18 mL) solution of methyl 3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate (1.40 g, 2.82 mmol). The reaction mixture was stirred at −78° C. for 30 minutes, and then stirred at −40° C. for 20 minutes. Iodomethane (2.6 mL, 42.3 mmol) was added, and the mixture was heated to room temperature and stirred for 4 hours. Water was added to the mixture to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=8%), thereby obtaining a syn-isomer mixture with a shorter retention time (isomer mixture 1) (505.7 mg, 31%) as an oily light yellow substance and an anti-isomer mixture with a longer retention time (isomer mixture 2) (853.3 mg, 52%) as an oily light yellow substance. The title compound is the anti-isomer mixture.
Isomer mixture 1: 1H NMR (400 MHz, CDCl3) δ 7.28-7.26 (3H, m), 7.17-7.15 (1H, m), 7.06 (1H, d, J=8.0 Hz), 6.89 (2H, br d, J=8.8 Hz), 6.82 (1H, d, J=3.6 Hz), 6.74 (1H, d, J=3.6 Hz), 4.47 (2H, s), 4.43 (2H, s), 4.25 (1H, d, J=10.8 Hz), 4.01-3.97 (2H, m), 3.96-3.90 (2H, m), 3.81 (3H, s), 3.43 (3H, s), 3.24-3.16 (1H, m), 2.25 (3H, s), 1.71 (3H, s), 1.20 (3H, d, J=6.8 Hz).
Isomer mixture 2: 1H NMR (400 MHz, CDCl3) δ 7.28-7.23 (3H, m), 7.11-7.10 (2H, m), 6.89 (2H, br d, J=8.8 Hz), 6.77 (1H, d, J=3.6 Hz), 6.71 (1H, br d, J=3.6 Hz), 4.48 (2H, s), 4.47 (2H, s), 4.27 (1H, d, J=11.2 Hz), 3.99-3.95 (2H, m), 3.93-3.90 (2H, m), 3.82 (3H, s), 3.58 (3H, s), 3.21-3.16 (1H, m), 2.28 (3H, s), 1.69 (3H, s), 1.05 (3H, d, J=6.8 Hz).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
2N hydrochloric acid (1.4 mL) was added to a tetrahydrofuran (2.8 mL) solution of methyl 3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methyl-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate, an anti-isomer mixture (isomer mixture 2) of Reference Example 209 (489 mg, 0.96 mmol), and the mixture was stirred at room temperature for 3 hours. The mixture was neutralized with a 1N sodium hydroxide aqueous solution and extracted with dichloromethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was distilled under reduced pressure, thereby obtaining the title compound (390.8 mg, 87%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.46 (1H, d, J=4.0 Hz), 7.29-7.24 (3H, m), 7.11 (2H, s), 6.92-6.89 (3H, m), 4.49 (2H, s), 4.48 (2H, s), 4.36 (1H, d, J=11.2 Hz), 3.82 (3H, s), 3.60 (3H, s), 3.25-3.21 (1H, m), 2.46 (3H, s), 2.26 (3H, s), 1.08 (3H, d, J=6.8 Hz).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
DDQ (681 mg, 3.0 mmol) was added at 0° C. to a dichloromethane/water (10/1) (18.2 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate, an anti-isomer mixture (700.9 mg, 1.5 mmol). The mixture was stirred at room temperature for 2.5 hours. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v) 6/4→4/6), thereby obtaining the title compound (436.3 mg, 84%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.46 (1H, d, J=4.0 Hz), 7.28 (1H, br s), 7.13 (2H, br s), 6.93 (1H, d, J=4.0 Hz), 4.68 (2H, d, J=5.6 Hz), 4.37 (1H, d, J=11.2 Hz), 3.60 (3H, s), 3.27-3.23 (1H, m), 2.46 (3H, s), 2.30 (3H, s), 1.09 (3H, d, J=6.8 Hz).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
DIPEA (430.5 μL, 2.52 mmol) and methanesulfonyl chloride (156.3 μL, 2.02 mmol) were added to a suspension of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2-methylpropanoate, an anti-isomer mixture (583.1 mg, 1.68 mmol) and lithium chloride (142.7 mg, 3.37 mmol) in dichloromethane (13.0 mL), and the mixture was stirred at room temperature for 16.5 hours. Water was added to the reaction solution, followed by extraction with dichloromethane. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=77/23→44/56), thereby obtaining the title compound (553.8 mg, 90%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.47 (1H, d, J=3.6 Hz), 7.21 (1H, s), 7.16 (2H, br s), 6.93 (1H, d, J=3.6 Hz), 4.57 (2H, s), 4.37 (1H, d, J=11.2 Hz), 3.61 (3H, s), 3.25-3.21 (1H, m), 2.47 (3H, s), 2.38 (3H, s), 1.09 (3H, d, J=7.2 Hz).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
A DMF (0.5 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2-methylpropanoate, an anti-isomer mixture (22.8 mg, 0.062 mmol), (R)-4-ethyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide (14.3 mg, 0.063 mmol), potassium carbonate (26.5 mg, 0.19 μmol), and tetrabutyl ammonium iodide (4.7 mg, 0.012 mmol) was stirred at 50° C. for 1.5 hours. The reaction solution was cooled to room temperature, and water was added, followed by extraction with ethyl acetate/hexane (1/1). The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=100/0→50/50), thereby obtaining the title compound (29.9 mg, 86%) as a colorless solid.
1H NMR (400 Mz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.47-7.46 (1H, m), 7.28-7.24 (2H, m), 7.22 (1H, d, J=8.0 Hz), 7.15 (2H, s), 7.10-7.06 (1H, m), 6.91 (1H, d, J=3.2 Hz), 4.61-4.53 (1H, m), 4.36 (1H, d, J=11.2 Hz), 4.06-3.97 (1H, m), 3.88-3.78 (1H, m), 3.75-3.67 (1H, m), 3.61-3.60 (3H, m), 3.24-3.15 (1H, m), 2.98-2.89 (1H, m), 2.46 (3H, s), 2.35-2.33 (3H, m), 1.73-1.61 (1H, m), 1.46-1.34 (1H, m), 1.09-1.04 (6H, m).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
A DMF (7.4 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2-methylpropanoate, an anti-isomer mixture (90.9 mg, 0.249 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (56.9 mg, 0.249 mmol), potassium carbonate (103.2 mg, 0.747 mmol), and tetrabutylammonium iodide (18.4 mg, 0.05 mmol) was stirred at room temperature for 4 hours. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=55/45→36/64), thereby obtaining the title compound (124.9 mg, 90%) as an oily light yellow substance.
1H NMR (400 MHz, CDCl3) δ 9.03 (1H, s), 8.67-8.65 (1H, m), 7.48-7.46 (1H, m), 7.17 (2H, s), 7.12-7.09 (2H, m), 6.93-6.92 (1H, m), 4.47-4.44 (1H, m), 4.38 (2H, d, J=12.0 Hz), 4.21-4.09 (1H, m), 3.61 (3H, s), 3.51-3.41 (1H, m), 3.23-3.11 (2H, m), 2.47 (3H, br s), 2.33 (3H, s), 1.74-1.63 (1H, m), 1.56-1.47 (1H, m), 1.08-1.02 (6H, m).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
2-(Trimethylsilyl)ethanol (0.37 mL, 2.58 mmol), DIPEA (0.27 mL, 1.55 mmol), and 4-dimethylaminopyridine (126.1 mg, 1.03 mmol) were added to a dimethylformamide (4.7 mL) solution of 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoic acid (248.9 mg, 0.52 mmol) and HATU (294.3 mg, 0.77 mmol). After the reaction mixture was stirred at room temperature for 22 hours, water was added, followed by extraction with hexane/ethyl acetate (1/1). The organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=100/0→85/15), thereby obtaining an anti-isomer mixture with a shorter retention time (isomer mixture 1) (74.7 mg, 25%) an oily colorless substance and a syn-isomer mixture with a longer retention time (isomer mixture 2) (36.0 mg, 12%) as an oily yellow substance. The title compound is the anti-isomer mixture.
Isomer mixture 1: 1H NMR (400 MHz, CDCl3) δ 7.26 (2H, br d, J=8.8 Hz), 7.21 (1H, s), 7.09 (2H, s), 6.88 (2H, br d, J=8.8 Hz), 6.67 (1H, s), 4.47 (2H, s), 4.43 (2H, s), 4.24 (1H, d, J=11.2 Hz), 4.10-4.05 (2H, m), 3.86 (3H, s), 3.80 (3H, s), 3.17-3.09 (1H, m), 2.41 (3H, s), 2.24 (3H, s), 1.04 (3H, d, J=6.8 Hz), 0.89-0.85 (2H, m), −0.00 (9H, s),
Isomer mixture 2: 1H NMR (400 MHz, CDCl3) δ 7.34-7.29 (3H, m), 7.23-7.11 (2H, m), 6.95 (2H, br d, J=8.8 Hz), 6.75 (1H, s), 4.55-4.51 (4H, m), 4.27 (1H, d, J=11.2 Hz), 4.00-3.94 (5H, m), 3.87 (3H, br s), 3.26-3.21 (1H, m), 2.51 (3H, s), 2.29 (3H, s), 1.28 (3H, d, J=6.8 Hz), 0.76-0.71 (2H, m), 0.00 (9H, s).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
2-(Trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(4-methoxybenzyl)oxy]methyl}-4-methylphenyl)-2-methylpropanoate, an anti-isomer mixture (isomer mixture 1) of Reference Example 215 (74.7 mg, 0.13 mmol), dichloromethane (3 mL), water (0.17 mL), and DDQ (34.9 mg, 0.15 mmol) were used as raw materials, and the same operation was performed as in Reference Example 20, thereby obtaining the title compound (57.9 mg, 98%) as an oily colorless substance.
1H NMR (400 MHz, CDCl3) δ 7.28 (1H, s), 7.12 (2H, br s), 6.70 (1H, s), 4.68-4.67 (2H, m), 4.27 (1H, d, J=11.2 Hz), 4.15-4.04 (2H, m), 3.90 (3H, s), 3.19-3.12 (1H, m), 2.43 (3H, s), 2.30 (3H, s), 1.74-1.71 (1H, m), 1.06 (3H, d, J=7.2 Hz), 0.91-0.87 (2H, m), 0.02 (9H, s).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
DIPEA (85.7 μL, 0.50 mmol) and methanesulfonyl chloride (29.0 μL, 0.38 mmol) were added to a dichloromethane (1.1 mL) suspension of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(hydroxymethyl)-4-methylphenyl]-2-methylpropanoate, an anti-isomer mixture (57.9 mg, 0.13 mmol) and lithium chloride (26.5 mg, 0.63 mmol), and the mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction solution, followed by extraction with dichloromethane. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure, thereby obtaining the title compound (77.1 mg, quant.) as an oily pale yellow substance.
1H NMR (400 MHz, CDCl3) δ 7.18 (1H, s), 7.13 (2H, br s), 6.68 (1H, s), 4.55 (2H, s), 4.25 (1H, d, J=11.2 Hz), 4.10-4.05 (2H, m), 3.88 (3H, s), 3.16-3.08 (1H, m), 2.42 (3H, s), 2.36 (3H, s), 1.04 (3H, d, J=7.2 Hz), 0.89-0.85 (2H, m), −0.00 (9H, s).
The anti-isomer mixture in the upper row above contains the two compounds in the lower row.
A DMF (3.4 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-[3-(chloromethyl)-4-methylphenyl]-2-methylpropanoate, an anti-isomer mixture (75.0 mg, 0.16 mmol), (R)-4-ethyl-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepine 1,1-dioxide (35.6 mg, 0.16 mmol), potassium carbonate (64.7 mg, 0.47 mmol), and tetrabutylamnonium iodide (11.5 mg, 0.031 mmol) was stirred at room temperature for 7 hours. Water was added to the reaction solution, followed by extraction with hexane/ethyl acetate (1/1). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=67/33→46/54), thereby obtaining the title compound (54.2 mg, 52%) as an oily pale yellow substance.
1H NMR (400 Mz, CDCl3) δ 9.02 (1H, s), 8.67-8.65 (1H, m), 7.16-7.09 (4H, m), 6.72 (1H, s), 4.47-4.35 (2H, m), 4.29-4.08 (4H, m), 3.92 (3H, br s), 3.52-3.41 (1H, m), 3.19-3.09 (2H, m), 2.44 (3H, s), 2.33 (3H, s), 1.75-1.64 (1H, m), 1.57-1.49 (1H, m), 1.06-1.02 (6H, m), 0.92-0.87 (2H, m), 0.02 (9H, s).
A 1M sodium hydroxide aqueous solution (3.8 mL, 3.8 mmol) was added to a methanol (10.0 mL)/THF (2.5 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate, an anti-isomer mixture (1.4099 g, 2.54 mmol), and the mixture was stirred at 100° C. for 1 hour by microwave irradiation. The reaction solution was cooled to room temperature, and the pH was adjusted to 4 with hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=100/1: isocratic, 20 min→1/1: isocratic, 40 min→MeOH/dichloromethane (v/v)=1/9: isocratic, 40 min), thereby obtaining the title compound (687.4 mg, 50%) as a white solid. A syn-isomer mixture (427.5 mg, 31%) with a shorter retention time than that of the title compound was also obtained. This syn-isomer mixture is identical to the syn-isomer mixture produced in Reference Example 219.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.49-7.47 (1H, m), 7.28-7.24 (1H, m), 7.21 (1H, br d, J=8.0 Hz), 7.17-7.12 (2H, m), 7.11-7.07 (1H, m), 6.96 (1H, d, J=3.6 Hz), 4.61-4.53 (1H, m), 4.34 (1H, d, J=11.2 Hz), 4.06-3.95 (1H, m), 3.89-3.78 (1H, m), 3.76-3.68 (1H, m), 3.23-3.15 (1H, m), 2.98-2.89 (1H, m), 2.46 (3H, s), 2.34-2.33 (3H, m), 1.75-1.58 (1H, m), 1.48-1.32 (1H, m), 1.11-1.05 (6H, m).
(2R,3S)/(2S,3R)-3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid (anti-isomer mixture) (9.48 g, 17.5 mmol) was separated into diastereomer 1 (4.16 g. 7.68 μmol, 44%) and diastereomer 2 (4.28 g, 7.90 mmol, 45%) by chiral HPLC (high performance liquid chromatography) under the following conditions. The title compound ((2R,3S)-3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid) (compound A1) was obtained as diastereomer 1. Diastereomer 2 is referred to as compound A2.
Compound A1 (diastereomer 1): 1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=8.0, 1.6 Hz), 7.53 (1H, td, J=8.0, 1.6 Hz), 7.47 (1H, d, J=4.0 Hz), 7.28-7.24 (1H, m), 7.22 (1H, d, J=8.0 Hz), 7.18-7.13 (2H, m), 7.07 (1H, s), 6.96 (1H, d, J=4.0 Hz), 4.58 (1H, d, J=14.4 Hz), 4.35 (1H, d, J=10.8 Hz), 4.06-3.97 (1H, m), 3.80 (1H, d, J=14.4 Hz), 3.72 (1H, dd, J=14.0, 10.4 Hz), 3.25-3.17 (1H, m), 2.91 (1H, d, J=14.0 Hz), 2.47 (3H, s), 2.34 (3H, s), 1.71-1.59 (1H, m), 1.42-1.35 (1H, m), 1.11-1.05 (6H, m),
Compound A2 (diastereomer 2): 1H NMR (400 MHz, CDCl3) δ 7.89 (1H, dd, J=7.6, 1.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.48 (1H, d, J=4.0 Hz), 7.28-7.24 (1H, m), 7.22 (1H, d, J=7.6 Hz), 7.17-7.12 (2H, m), 7.11 (1H, s), 6.96 (1H, d, J=4.0 Hz), 4.54 (1H, d, J=14.4 Hz), 4.35 (1H, d, J=11.2 Hz), 4.06-4.00 (1H, m), 3.87 (1H, d, J=14.4 Hz), 3.70 (1H, dd, J=14.8, 10.8 Hz), 3.26-3.18 (1H, m), 2.96 (1H, d, J=14.8 Hz), 2.47 (3H, s), 2.33 (3H, s), 1.75-1.64 (1H, m), 1.48-1.38 (1H, m), 1.11 (3H, d, J=6.8 Hz), 1.07 (3H, t, J=7.2 Hz).
Lithium hydroxide (10.8 mg, 0.45 mmol) was added to an H2O/methanol/THF (0.48 mL/0.12 mL/0.48 mL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate, an anti-isomer mixture (124.9 mg, 0.224 mmol), and the mixture was stirred at 60° C. for 6 hours. 1N hydrochloric acid was added to the reaction solution, followed by extraction with dichloromethane. The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel column chromatography (hexane/ethyl acetate (v/v)=57/43→7/93→MeOH/dichloromethane (v/v)=20/80), thereby obtaining the title compound (47.4 mg, 39%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.67-8.65 (1H, m), 7.49-7.47 (1H, m), 7.17 (2H, s), 7.12-7.10 (2H, m), 6.99-6.97 (1H, m), 4.47-4.36 (3H, m), 4.22-4.10 (1H, m), 3.50-3.40 (1H, m), 3.26-3.12 (2H, m), 2.47 (3H, s), 2.33 (3H, s), 1.74-1.63 (1H, m), 1.56-1.48 (1H, m), 1.12 (3H, d, J=6.8 Hz), 1.06-1.02 (3H, m).
(2R,3S)/(2S,3R)-3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid (anti-isomer mixture)(4.9 g, 9.0 mmol) was separated into diastereomer 1 (1.7 g, 3.1 mmol, 35%) and diastereomer 2 (1.4 g, 2.6 mmol, 29%) by chiral SFC (supercritical fluid chromatography) under the following conditions. The title compound ((2R,3S)-3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid)(compound B1) was obtained as diastereomer 1. Diastereomer 2 is referred to as compound B2.
Compound B1 (diastereomer 1): 1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.66 (1H, d, J=5.6 Hz), 7.48 (1H, d, J=4.0 Hz), 7.19-7.15 (2H, m), 7.11 (1H, d, J=5.6 Hz), 7.10 (1H, s), 6.97 (1H, d, J=4.0 Hz), 4.45 (1H, d, J=14.0 Hz), 4.43-4.39 (1H, m), 4.38 (1H, d, J=11.2 Hz), 4.12 (1H, d, J=14.0 Hz), 3.47 (1H, dd, J=15.2, 11.2 Hz), 3.27-3.19 (1H, m), 3.14 (1H, br d, J=15.2 Hz), 2.47 (3H, s), 2.33 (3H, s), 1.71-1.61 (1H, m), 1.55-1.45 (1H, m), 1.11 (3H, d, J=6.8 Hz), 1.04 (3H, t, J=7.2 Hz),
Compound B2 (diastereomer 2): 1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.65 (1H, d, J=5.6 Hz), 7.49 (1H, d, J=3.6 Hz), 7.17 (2H, br s), 7.12 (1H, s), 7.11 (1H, d, J=5.6 Hz), 6.98 (1H, d, J=3.6 Hz), 4.48-4.45 (1H, m), 4.37 (2H, d, J=13.2 Hz), 4.20 (1H, d, J=14.0 Hz), 3.43 (1H, dd, J=14.8, 11.2 Hz), 3.24-3.20 (1H, m), 3.17 (1H, br d, J=14.8 Hz), 2.47 (3H, s), 2.33 (3H, s), 1.75-1.64 (1H, m), 1.58-1.48 (1H, m), 1.11 (3H, d, J=7.2 Hz), 1.03 (3H, t, J=7.2 Hz).
A 1M tetrabutylamnonium fluoride THF solution (315 μL, 0.32 mmol) was added to a THF (0.7 mL) solution of 2-(trimethylsilyl)ethyl 3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoate, an anti-isomer mixture (42.4 Mg, 0.063 mmol), and the mixture was stirred at room temperature for 2 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with dichloromethane/methanol (95/5). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v)=100/0→99/1), thereby obtaining the title compound (22.5 mg, 62%) as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.65-8.63 (1H, m), 7.14-7.08 (4H, m), 6.73 (1H, s), 4.46-4.35 (2H, m), 4.29-4.26 (1H, m), 4.22-4.10 (1H, m), 3.87-3.86 (3H, m), 3.55-3.44 (1H, m), 3.22-3.08 (2H, m), 2.38 (3H, br s), 2.31 (3H, s), 1.73-1.65 (1H, m), 1.54-1.49 (1H, m), 1.05-1.01 (6H, m).
(2R,3S)/(2S,3R)-3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid (anti-isomer mixture) (49 mg, 0.086 mmol) was separated into diastereomer 1 (29 mg, 0.051 mmol, 59%, containing solvent) and diastereomer 2 (22 mg, 0.038 mmol, 45%, containing solvent) by chiral HPLC under the following conditions. The title compound ((2R,3S)-3-(5-acetyl-4-methoxythiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methylpropanoic acid) (compound C1) was obtained as diastereomer 1. Diastereomer 2 is referred to as compound C2.
Compound C1 (diastereomer 1): 1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.66 (1H, d, J=5.6 Hz), 7.17 (2H, s), 7.12 (1H, s), 7.11 (1H, d, J=5.6 Hz), 6.76 (1H, s), 4.44 (1H, d, J=14.4 Hz), 4.42-4.38 (1H, m), 4.29 (1H, d, J=10.4 Hz), 4.12 (1H, d, J=14.4 Hz), 3.92 (3H, s), 3.48 (1H, dd, J=14.4, 10.4 Hz), 3.23-3.14 (2H, m), 2.44 (3H, s), 2.32 (3H, s), 1.72-1.64 (1H, m), 1.53-1.51 (1H, m), 1.11 (3H, d, J=6.8 Hz), 1.04 (3H, t, J=7.6 Hz),
Compound C2 (diastereomer 2): 1H NMR (400 MHz, CDCl3) δ 9.02 (1H, s), 8.66 (1H, d, J=5.6 Hz), 7.17 (2H, s), 7.15 (1H, s), 7.11 (1H, d, J=5.6 Hz), 6.76 (1H, s), 4.51-4.45 (1H, m), 4.37 (1H, d, J=14.0 Hz), 4.29 (1H, d, J=10.8 Hz), 4.20 (1H, d, J=14.0 Hz), 3.93 (3H, s), 3.44 (1H, dd, J=14.8, 11.2 Hz), 3.23-3.17 (2H, m), 2.44 (3H, s), 2.32 (3H, s), 1.75-1.66 (1H, m), 1.58-1.51 (1H, m), 1.11 (3H, d, J=7.2 Hz), 1.04 (3H, t, J=7.6 Hz).
Lithium iodide (56.2 mg, 0.42 mmol) was added to a pyridine (306 μL) solution of methyl 3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoate (40.0 mg, 0.070 mmol), and the mixture was heated to reflux at 120° C. for 48 hours. The reaction solution was cooled to room temperature, and the solvent was distilled under reduced pressure. The pH was adjusted to 4 with 1N hydrochloric acid, followed by extraction with dichloromethane. The obtained organic layer was dried over sodium sulfate, and the solvent was distilled under reduced pressure. The obtained residue was purified by preparative thin-layer chromatography (methanol/ethyl acetate (v/v)=2/98), thereby obtaining the title compound (6.0 mg, 15%) as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 9.00 (1H, br s), 8.66-8.63 (1H, m), 7.54 (1H, d, J=3.6 Hz), 7.30-7.26 (2H, m), 7.16-7.10 (2H, m), 7.05-7.03 (1H, m), 4.75-4.74 (1H, m), 4.46-4.37 (2H, m), 4.17-4.11 (1H, m), 3.46-3.43 (1H, m), 3.20-3.14 (1H, m), 2.50 (3H, s), 2.32 (3H, s), 1.73-1.63 (1H, m), 1.57-1.47 (1H, m), 1.32 (3H, s), 1.27-1.26 (3H, m), 1.06-1.02 (3H, m).
3-(5-acetylthiophen-2-yl)-3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-pyrido[4,3-b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2,2-dimethylpropanoic acid (49 mg, 0.088 mmol) was separated into diastereomer 1 (27 mg, 0.049 mmol, 55%, containing solvent) and diastereomer 2 (28 mg, 0.050 mmol, 57%, containing solvent) by chiral HPLC (high performance liquid chromatography) under the following conditions. Diastereomer 1 was eluted before diastereomer 2. The title compound (compound D1) was obtained as diastereomer 1. Diastereomer 2 is referred to as compound D2.
Compound D1 (diastereomer 1): 1H NMR (400 MHz, CDCl3) δ 9.00 (1H, s), 8.65 (1H, d, J=5.6 Hz), 7.53 (1H, d, J=4.0 Hz), 7.30-7.26 (2H, m), 7.15 (1H, d, J=7.6 Hz), 7.11 (1H, d, J=5.6 Hz), 7.04 (1H, d, J=4.0 Hz), 4.74 (1H, s), 4.46-4.41 (1H, m), 4.39 (1H, d, J=14.4 Hz), 4.16 (1H, d, J=14.4 Hz), 3.46 (1H, dd, J=14.8, 10.8 Hz), 3.16 (1H, dd, J=14.8, 2.0 Hz), 2.50 (3H, s), 2.32 (3H, s), 1.71-1.61 (1H, m), 1.56-1.47 (1H, m), 1.33 (3H, s), 1.27 (3H, s), 1.03 (3H, t, J=7.2 Hz),
Compound D2 (diastereomer 2): 1H NMR (400 MHz, CDCl3) δ 9.01 (1H, s), 8.65 (1H, d, J=5.2 Hz), 7.53 (1H, d, J=3.6 Hz), 7.30-7.26 (2H, m), 7.15 (1H, d, J=8.0 Hz), 7.11 (1H, d, J=5.2 Hz), 7.03 (1H, d, J=3.6 Hz), 4.72 (1H, s), 4.48-4.44 (1H, m), 4.39 (1H, d, J=14.4 Hz), 4.16 (1H, d, J=14.4 Hz), 3.45 (1H, dd, J=14.8, 10.8 Hz), 3.18 (1H, dd, J=14.8, 2.0 Hz), 2.50 (3H, s), 2.32 (3H, s), 1.73-1.66 (1H, m), 1.57-1.52 (1H, m), 1.33 (3H, s), 1.28 (3H, s), 1.04 (3H, t, J=7.2 Hz).
Concentrated hydrochloric acid (100 μL) was added to a THF (3.0 mL) solution of methyl 3-(3-{[(R)-4-ethyl-1,1-dioxide-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepin-2-yl]methyl}-4-methylphenyl)-2-methyl-3-[5-(2-methyl-1,3-dioxolan-2-yl)thiophen-2-yl]propanoate of Reference Example 157 (mixture of isomer mixture 1 and isomer mixture 2 of Reference Example 157) (46 mg, 0.077 mmol), and the mixture was stirred at room temperature for 7 hours. The reaction mixture was diluted with water, followed by extraction with dichloromethane. The organic layer was washed with water and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The obtained residue was dissolved in methanol/dichloromethane (1/1) (1.0 mL), a 4N sodium hydroxide aqueous solution (100 μL, 0.4 mmol) was added, and the mixture was stirred at 60° C. for 6 hours. 1N hydrochloric acid was added to the mixture, followed by extraction with methanol/dichloromethane (1/10). The organic layer was washed with saturated saline and dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was separated into a syn-isomer mixture (6.9 mg, 16%) and an anti-isomer mixture (9.6 mg, 23%) by preparative thin-layer chromatography (hexane/ethyl acetate (v/v)=1/4). The title compound was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.88 (1H, d, J=7.6 Hz), 7.53 (1H, td, J=7.6, 1.6 Hz), 7.50-7.49 (1H, m), 7.28-7.17 (3H, m), 7.14-7.09 (2H, m), 6.95-6.92 (1H, m), 4.55-4.50 (1H, m), 4.30 (1H, d, J=10.8 Hz), 4.05-3.97 (1H, m), 3.81-3.66 (2H, m), 3.26-3.15 (1H, m), 2.90 (1H, br d, J=15.2 Hz), 2.48 (3H, s), 2.31 (3H, br s), 1.69-1.59 (1H, m), 1.47-1.37 (1H, m), 1.22 (3H, d, J=6.8 Hz), 1.12-1.05 (3H, m).
X-ray single crystal structure analysis was performed to determine the unknown absolute configuration of the two asymmetric centers of compound A1. A sample was crystallized using ethyl acetate and hexane. The crystallographic data and crystal structure obtained are shown in Table 10 and
The relative configurations and absolute configurations of compound A2, compounds B1/B2, and compounds C1/C2 were determined from H-NMR data based on the three-dimensional structure of compound A1.
As a result of comparing NMR charts of compounds A1/A2, focusing on two protons (* and **) that had large differences in chemical shift values around the asymmetric centers, the proton indicated by * was observed at 7.07 ppm in compound A1, whereas the proton indicated by * was observed at 7.11 ppm in compound A2; compound A2 showed a downfield shift compared with compound A1. The proton indicated by ** was observed at 4.58 ppm and 3.80 ppm in compound A1, whereas the proton indicated by ** was observed at 4.54 ppm and 3.87 ppm in compound A2; compound A2 showed a shift so that the distance between the two protons was narrowed. Since the same behavior as in compounds A1/A2 was observed in compounds B1/B2 and compounds C1/C2 for the chemical shift values of the protons indicated by * and **, the absolute configurations of compounds B1/B2 and compounds C1/C2 were determined so that the individual behaviors of the corresponding protons were consistent.
Compounds A1/A2, compounds B1/B2, compounds C1/C2, and compounds D1/D2 were used as test substances. Binding assay and reporter assay were performed as in Test Example 1-1 and Test Example 1-2. In addition, concentrations that did not affect cell viability were determined as follows.
To confirm cell viability, HCE-T cells were seeded at 10000 cells per well in a 96-well polystyrene microplate (IWAKI). The cells were cultured in a CO2 incubator at 37° C. for 16 hours to allow the cells to adhere. The culture of the HCE-T cells was performed using DMEM/F12 medium containing 10 ng/mL hEGF, 5 μg/mL insulin, 5% FBS, and 40 μg/mL gentamicin.
Each test substance was dissolved in dimethyl sulfoxide to prepare a stock solution with a concentration that is 1000 times the test concentration. DMEM/F12 medium containing 40 μg/mL gentamicin was used as assay medium. The medium containing serum and growth factors was removed and replaced with assay medium in which each test substance was appropriately serially diluted, and the cell viability was measured after 24 hours. Cell Counting Kit-8 (Dojindo Laboratories) was added to each well in an amount that is 1/10 the amount of the medium. Color reaction was performed for 1 hour in a CO2 incubator, and absorbance at 450 nm was measured with a microplate reader (Corona Electric Co., Ltd.). The concentration of each test substance that does not affect cell viability (cytotoxic concentration) was calculated by setting the absorbance in a well containing no test substance as 100% viability, and creating a calibration curve between two concentrations across the absorbance of 100% viability. The test was performed at N=3.
Table 12 shows the results of IC50 (nM, binding assay), EC50 (nM, reporter assay), and cytotoxic concentration (μM, cell viability test) of the diastereomers of each compound (compound n1 and compound n2 (n is A, B, C, or D)). The positions of the symbols in the compounds in Table 12 are shown in the following formula. Each experimental value is expressed as the mean. In comparisons of IC50 between the diastereomers of the compounds, n1 showed 5 times or more higher activity than n2 (N=2). In comparisons of EC50 between the diastereomers of the compounds, n1 showed 50 times or more higher activity than n2. In comparisons of cytotoxic concentration, n2 showed cytotoxicity at a significantly lower concentration than n1. Statistical analysis was performed using Student's t-test in comparisons of EC50 and cytotoxic concentration between the diastereomers (compound n1 and compound n2) of the compounds, and results were considered significantly different if the p value was less than 0.05, and shown in Table 12 (N=3, *0.01<p<0.05, **p<0.01, vs each compound n1).
The above results and the results of Test Example 1 showed that among the compounds represented by formula (X) and prodrugs thereof, the compound represented by formula (I), whose three-dimensional structure was partially specified:
wherein R1 represents an alkyl group; R2 represents an optionally substituted thienyl group; R4 and R5 are identical or different and represent a hydrogen atom or an optionally substituted alkyl group, or R4 and R5 bind with each other to form —NH—CH═N—; R6 represents an optionally substituted alkyl group; R7 represents a hydroxy group, a hydrolyzable group, or —NR71R72 wherein R71 and R72 are identical or different and represent a hydrogen atom or a —[C(═O)]0-1-hydrocarbon group; A1, A2, A3, and A4 are identical or different and represent CH or N wherein the number of N is 1 or less; and Z represents a hydrogen atom or a halogen atom, and compounds of the less-polar group of two groups of diastereomers in which the carbon atom indicated by * in formula (II) is an asymmetric carbon atom:
wherein R1a and R1b represents an alkyl group; R2 represents an optionally substituted thienyl group; R4 and R5 are identical or different and represent a hydrogen atom or an optionally substituted alkyl group, or R4 and R5 bind with each other to form —NH—CH═N—; R4 represents an optionally substituted alkyl group; R7 represents a hydroxy group, a hydrolyzable group, or —NR71R72 wherein R71 and R72 are identical or different and represent a hydrogen atom or a —[C(═O)]0-1-hydrocarbon group; A1, A2, A3, and A4 are identical or different and represent CH or N wherein the number of N is 1 or less; and Z represents a hydrogen atom or a halogen atom, have higher Nrf2-activating action and are less cytotoxic.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-218261 | Dec 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/048868 | 12/28/2021 | WO |
