The present invention relates to an agricultural composition for controlling or preventing plant diseases caused by plant pathogenic microbes, comprising an amide compound, a salt thereof or a hydrate thereof, and a method for controlling or preventing plant diseases caused by plant pathogenic microbes, which comprises applying an effective amount of the aforementioned agricultural composition to useful crops.
Agricultural compositions for controlling plant diseases have conventionally been known. However, it has always desired to produce a more highly active agricultural composition for controlling plant diseases. On the other hand, the amide compound described in PATENT DOCUMENT 1 and the like have been disclosed and thus have been publicly known.
It is an object of the present invention to provide: an agricultural composition for controlling or preventing plant diseases caused by plant pathogenic microbes; a method for controlling or preventing plant diseases caused by plant pathogenic microbes, which comprises applying an effective amount of the aforementioned agricultural composition to useful crops; etc.
As a result of intensive studies, the present inventor has found that a compound represented by the following formula (1) has an excellent effect for controlling or preventing plant diseases caused by plant pathogenic microbes, thereby completing the present invention. Compound represented by formula (1):
wherein Z represents an oxygen atom, a sulfur atom, or NRZ wherein RZ represents a C1-6 alkoxy group or a cyano group;
E represents a furyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a thienyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a pyrrolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a tetrazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a thiazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a pyrazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, or a phenyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2; and
each of R1, R2 and R3 independently represents a hydrogen atom or a group selected from the substituent group a-1 and the substituent group a-2;
[Substituent Group a-1]
halogen atom, amino group, hydroxyl group, mercapto group, cyano group, formyl group, carboxyl group, C1-8 alkyl group, C2-9 alkenyl group, C2-9 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C3-8 cycloalkylidene C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, C6-10 aryl C2-6 alkenyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-8 alkoxy group, C3-9 alkenyloxy group, C3-9 alkynyloxy group, C3-8 cycloalkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C1-8 alkylthio group, C3-9 alkenylthio group, C3-9 alkynylthio group, C3-8 cycloalkylthio group, C6-10 arylthio group, C3-8 cycloalkyl C1-6 alkylthio group, C6-10 aryl C1-6 alkylthio group, 5- to 10-membered heterocyclic C1-6 alkylthio group, mono-C1-8 alkylamino group, mono-C3-9 alkenylamino group, mono-C3-9 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C6-10 arylamino group, mono-C3-8 cycloalkyl C1-6 alkylamino group, mono-C6-10 aryl C1-6 alkylamino group, mono-5- to 10-membered heterocyclic C1-6 alkylamino group, di-C1-6 alkylamino group, N—C3-9 alkenyl-N—C1-8 alkylamino group, N—C3-9 alkynyl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl-N—C1-8 alkylamino group, N—C6-10 aryl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl C1-6 alkyl-N—C1-8 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-8 alkylamino group, N-5- to 10-membered heterocyclic C1-6 alkyl-N—C1-8 alkylamino group, C1-8 alkylcarbonyl group, C6-10 arylcarbonyl group, C1-8 alkoxycarbonyl group, C1-8 alkylsulfonyl group, C1-8 alkylsulfinyl group, a group represented by a formula —C(═N—Ra1)Ra2 (wherein Ra1 represents a hydroxyl group or a C1-8 alkoxy group; and Rat represents a hydrogen atom or a C1-8 alkyl group), C6-10 aryloxy C1-6 alkyl group, 5- to 10-membered heterocyclic oxy C1-6 alkyl group and C1-3 trialkylsilyl C2-9 alkynyl group; and
[Substituent Group a-2]
C1-8 alkyl group, C2-9 alkenyl group, C2-9 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-8 alkoxy group, C3-9 alkenyloxy group, C3-9 alkynyloxy group, C3-8 cycloalkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C1-8 alkylthio group, C3-9 alkenylthio group, C3-9 alkynylthio group, C3-8 cycloalkylthio group, C6-10 arylthio group, C3-8 cycloalkyl C1-6 alkylthio group, C6-10 aryl C1-6 alkylthio group, 5- to 10-membered heterocyclic C1-6 alkylthio group, mono-C1-8 alkylamino group, mono-C3-9 alkenylamino group, mono-C3-9 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C6-10 arylamino group, mono-C3-8 cycloalkyl C1-6 alkylamino group, mono-C6-10 aryl C1-6 alkylamino group, mono-5- to 10-membered heterocyclic C1-6 alkylamino group, di-C1-6 alkylamino group, N—C3-9 alkenyl-N—C1-8 alkylamino group, N—C3-9 alkynyl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl-N—C1-8 alkylamino group, N—C6-10 aryl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl C1-6 alkyl-N—C1-8 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-8 alkylamino group, N-5- to 10-membered heterocyclic C1-6 alkyl-N—C1-8 alkylamino group, C6-10 aryloxy C1-6 alkyl group and 5- to 10-membered heterocyclic oxy C1-6 alkyl group;
wherein each group described in the substituent group a-2 has one to three substituents selected from the following substituent group b:
halogen atom, hydroxyl group, mercapto group, cyano group, carboxyl group, amino group, carbamoyl group, nitro group, C1-6 alkyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C1-6 alkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C1-6 alkoxycarbonyl group, C1-6 alkylthio group, C1-6 alkylsulfonyl group, trifluoromethyl group, trifluoromethoxy group, mono-C1-6 alkylamino group, di-C1-6 alkylamino group, mono-C6-10 arylamino group optionally having one amino group or one aminosulfonyl group, and N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group optionally having one amino group; a salt thereof or a hydrate thereof.
That is to say, the present invention provides the following (1) to (3):
(1) an agricultural composition (hereinafter referred to as the agricultural composition of the present invention at times) comprising the compound represented by the above formula (1), a salt thereof or a hydrate thereof (hereinafter referred to as the present compound at times), which is used for controlling or preventing plant diseases caused by plant pathogenic microbes (except for Aspergillus),
(2) a method for controlling or preventing plant diseases caused by plant pathogenic microbes (except for Aspergillus), comprising applying an effective amount of the agricultural composition to useful crops, and
(3) use of the compound represented by formula (1), a salt thereof or a hydrate thereof for production of the agricultural composition of the present invention.
According to the present invention, it becomes possible to provide an agricultural composition for controlling or preventing plant diseases caused by plant pathogenic microbes (except for Aspergillus), a method for controlling or preventing plant diseases caused by plant pathogenic microbes (except for Aspergillus), comprising applying an effective amount of the agricultural composition to useful crops etc.
In the formula (1) that represents the present compound, each of R1, R2 and R3 independently represents a hydrogen atom or a group selected from the aforementioned substituent group a-1 and substituent group a-2, and preferably represents a hydrogen atom or a group selected from the following substituent group c-1 and substituent group c-2:
[Substituent Group c-1]
halogen atom, amino group, C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, C6-10 aryl C2-6 alkenyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, mono-C1-6 alkylamino group, mono-C3-6 alkenylamino group, mono-C3-6 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C1-6 arylamino group, mono-C6-10 cycloalkyl C1-6 alkylamino group, mono-C1-6 aryl C1-6 alkylamino group, mono-5- to 10-membered heterocyclic C1-6 alkylamino group, C2-6 alkylcarbonyl group and a group represented by a formula —C(═N—OH)Ra2 wherein Ra2 has the same meanings as defined above; and
[Substituent Group c-2]
C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, mono-C1-6 alkylamino group, mono-C3-6 alkenylamino group, mono-C3-6 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C6-10 arylamino group, mono-C3-8 cycloalkyl C1-6 alkylamino group, mono-C6-10 aryl C1-6 alkylamino group and mono-5- to 10-membered heterocyclic C1-6 alkylamino group; wherein each group described in the substituent group c-2 has one to three substituents selected from the following substituent group d:
halogen atom, hydroxyl group, carboxyl group, amino group, carbamoyl group, C1-6 alkyl group, C1-6 alkoxy group, C1-6 alkylthio group, mono-C1-6 alkylamino group, di-C1-6 alkylamino group, mono-C6-10 arylamino group optionally having one amino group or one aminosulfonyl group, N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group optionally having one amino group, cyano group, C6-10 aryl group, 5- to 10-membered heterocyclic group and C1-6 alkoxycarbonyl group.
In the formula (1), each of R1, R2 and R3 more preferably represents a hydrogen atom or a group selected from the following substituent group c-11 and substituent group c-12:
[Substituent Group c-11]
halogen atom, amino group, C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl group, C3-8 cycloalkyl C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C3-8 cycloalkyl C1-6 alkoxy group, mono-C1-6 alkylamino group, mono-C3-6 alkenylamino group, mono-C3-6 alkynylamino group, mono-C3-8 cycloalkylamino group and mono-C3-8 cycloalkyl C1-6 alkylamino group; and
[Substituent Group c-12]
C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl group, C3-8 cycloalkyl C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C3-8 cycloalkyl C1-6 alkoxy group, mono-C1-6 alkylamino group, mono-C3-6 alkenylamino group, mono-C3-6 alkynylamino group, mono-C3-8 cycloalkylamino group, and mono-C3-8 cycloalkyl C1-6 alkylamino group;
wherein each group described in the substituent group c-12 has one to three substituents selected from the following substituent group d1:
[Substituent Group d1]
halogen atom, hydroxyl group, carboxyl group, amino group, carbamoyl group, C1-6 alkyl group, C1-6 alkoxy group, C1-6 alkylthio group, mono-C1-6 alkylamino group, di-C1-6 alkylamino group, and cyano group.
In the formula (1), each of R1, R2 and R3 further preferably represents a hydrogen atom or a group selected from the following substituent group c-21 and substituent group c-22:
[Substituent Group c-21]
halogen atom, amino group, C1-6 alkyl group, C1-6 alkoxy group and mono-C1-6 alkylamino group; and
[Substituent Group c-22]
C1-6 alkyl group, C1-6 alkoxy group and mono-C1-6 alkylamino group;
wherein each group described in the substituent group c-22 has one to three substituents selected from the following substituent group d2:
[Substituent group d2]
halogen atom, C1-6 alkoxy group and C1-6 alkylthio group.
In the formula (1), still further preferably, R1 represents a hydrogen atom, R2 represents a hydrogen atom or a halogen atom (particularly, a fluorine atom or a chlorine atom), and R3 represents a hydrogen atom, a halogen atom (particularly, a fluorine atom or a chlorine atom), an amino group, a mono-C1-3 alkylamino group, C1-3 alkyl group, C1-3 alkoxy group, or a C1-3 alkoxy C1-3 alkyl group.
Moreover, as a combination of R1, R2 and R3 in the compound represented by the formula (1), a combination in which R1 represents a hydrogen atom, R2 represents a hydrogen atom or a halogen atom, and R3 represents a hydrogen atom or a group selected from the substituent group c-21 and the substituent group c-22, is preferable. Further, a combination in which R1, R2 and R3 are all hydrogen atoms is more preferable.
Z in the formula (1) representing the present compound represents an oxygen atom, a sulfur atom, or NRZ wherein RZ represents a C1-6 alkoxy group or a cyano group, and such Z preferably represents an oxygen atom.
E in the formula (1) representing the present compound represents a furyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a thienyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a pyrrolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a tetrazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a thiazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, a pyrazolyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2, or a phenyl group that may optionally have one or two substituents selected from the following substituent group a-1 and substituent group a-2:
[Substituent Group a-1]
halogen atom, amino group, hydroxyl group, mercapto group, cyano group, formyl group, carboxyl group, C1-8 alkyl group, C2-9 alkenyl group, C2-9 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C3-8 cycloalkylidene C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, C6-10 aryl C2-6 alkenyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-8 alkoxy group, C3-9 alkenyloxy group, C3-9 alkynyloxy group, C3-8 cycloalkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C1-8 alkylthio group, C3-9 alkenylthio group, C3-9 alkynylthio group, C3-8 cycloalkylthio group, C6-10 arylthio group, C3-8 cycloalkyl C1-6 alkylthio group, C6-10 aryl C1-6 alkylthio group, 5- to 10-membered heterocyclic C1-6 alkylthio group, mono-C1-8 alkylamino group, mono-C3-9 alkenylamino group, mono-C3-9 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C6-10 arylamino group, mono-C3-8 cycloalkyl C1-6 alkylamino group, mono-C6-10 aryl C1-6 alkylamino group, mono-5- to 10-membered heterocyclic C1-6 alkylamino group, di-C1-6 alkylamino group, N—C3-9 alkenyl-N—C1-8 alkylamino group, N—C3-9 alkynyl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl-N—C1-8 alkylamino group, N—C6-10 aryl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl C1-6 alkyl-N—C1-8 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-8 alkylamino group, N-5- to 10-membered heterocyclic C1-6 alkyl-N—C1-8 alkylamino group, C1-8 alkylcarbonyl group, C6-10 arylcarbonyl group, C1-8 alkoxycarbonyl group, C1-8 alkylsulfonyl group, C1-8 alkylsulfinyl group, a group represented by a formula —C(═N—Ra1)Ra2 (wherein Ra1 represents a hydroxyl group or a C1-8 alkoxy group; and Rat represents a hydrogen atom or a C1-8 alkyl group), C6-10 aryloxy C1-6 alkyl group, 5- to 10-membered heterocyclic oxy C1-6 alkyl group and C1-3 trialkylsilyl C2-9 alkynyl group; and
[Substituent Group a-2]
C1-8 alkyl group, C2-9 alkenyl group, C2-9 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-8 alkoxy group, C3-9 alkenyloxy group, C3-9 alkynyloxy group, C3-8 cycloalkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C1-8 alkylthio group, C3-9 alkenylthio group, C3-9 alkynylthio group, C3-8 cycloalkylthio group, C6-10 arylthio group, C3-8 cycloalkyl C1-6 alkylthio group, C6-10 aryl C1-6 alkylthio group, 5- to 10-membered heterocyclic C1-6 alkylthio group, mono-C1-8 alkylamino group, mono-C3-9 alkenylamino group, mono-C3-9 alkynylamino group, mono-C3-8 cycloalkylamino group, mono-C6-10 arylamino group, mono-C3-8 cycloalkyl C1-6 alkylamino group, mono-C6-10 aryl C1-6 alkylamino group, mono-5- to 10-membered heterocyclic C1-6 alkylamino group, di-C1-6 alkylamino group, N—C3-9 alkenyl-N—C1-8 alkylamino group, N—C3-9 alkynyl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl-N—C1-8 alkylamino group, N—C6-10 aryl-N—C1-8 alkylamino group, N—C3-8 cycloalkyl C1-6 alkyl-N—C1-8 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-8 alkylamino group, N-5- to 10-membered heterocyclic C1-6 alkyl-N—C1-8 alkylamino group, C6-10 aryloxy C1-6 alkyl group and 5- to 10-membered heterocyclic oxy C1-6 alkyl group;
wherein each group described in the substituent group a-2 has one to three substituents selected from the following substituent group b:
halogen atom, hydroxyl group, mercapto group, cyano group, carboxyl group, amino group, carbamoyl group, nitro group, C1-6 alkyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C1-6 alkoxy group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C1-6 alkoxycarbonyl group, C1-6 alkylthio group, C1-6 alkylsulfonyl group, trifluoromethyl group, trifluoromethoxy group, mono-C1-6 alkylamino group, di-C1-6 alkylamino group, mono-C6-10 arylamino group optionally having one amino group or one aminosulfonyl group and N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group optionally having one amino group.
E preferably represents a furyl group that may optionally have one or two substituents selected from the following substituent group e-1 and substituent group e-2, a thienyl group that may optionally have one or two substituents selected from the following substituent group e-1 and substituent group e-2, a pyrrolyl group that may optionally have one or two substituents selected from the following substituent group e-1 and substituent group e-2, or a phenyl group that may optionally have one or two substituents selected from the following substituent group e-1 and substituent group e-2:
[Substituent Group e-1]
halogen atom, C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C6-10 aryl group, C3-8 cycloalkyl C1-6 alkyl group, C3-8 cycloalkylidene C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, C6-10 aryl C2-6 alkenyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C6-10 aryloxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C6-10 arylthio group, C6-10 aryl C1-6 alkylthio group, mono-C6-10 arylamino group, mono-C6-10 aryl C1-6 alkylamino group, N—C6-10 aryl-N—C1-6 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group, C6-10 aryloxy C1-6 alkyl group, and 5- to 10-membered heterocyclic oxy C1-6 alkyl group; and
[Substituent Group e-2]
C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C6-10 aryl group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, 5- to 10-membered heterocyclic C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, C6-10 aryloxy group, C3-8 cycloalkyl C1-6 alkoxy group, C6-10 aryl C1-6 alkoxy group, 5- to 10-membered heterocyclic C1-6 alkoxy group, C6-10 arylthio group, C6-10 aryl C1-6 alkylthio group, mono-C6-10 arylamino group, mono-C6-10 aryl C1-6 alkylamino group, N—C6-10 aryl-N—C1-6 alkylamino group, N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group, C6-10 aryloxy C1-6 alkyl group and 5- to 10-membered heterocyclic oxy C1-6 alkyl group;
wherein each group described in the substituent group e-2 has one to three substituents selected from the following substituent group f:
halogen atom, hydroxyl group, cyano group, amino group, nitro group, C3-8 cycloalkyl group, C1-6 alkoxy group, C1-6 alkylthio group, C6-10 aryloxy group, 5- to 10-membered heterocyclic oxy group, C1-6 alkoxycarbonyl group, C1-6 alkylsulfonyl group, mono-C6-10 arylamino group, trifluoromethyl group, trifluoromethoxy group and C1-6 alkyl group.
More preferably, E represents a furyl group that may optionally have one or two substituents selected from the following substituent group g-1 and substituent group g-2, a thienyl group that may optionally have one or two substituents selected from the following substituent group g-1 and substituent group g-2, a pyrrolyl group that may optionally have one or two substituents selected from the following substituent group g-1 and substituent group g-2 or a phenyl group that may optionally have one or two substituents selected from the following substituent group g-1 and substituent group g-2.
Further preferably, E represents a furyl group that may optionally have one substituent selected from the following substituent group g-1 and substituent group g-2, a thienyl group that may optionally have one substituent selected from the following substituent group g-1 and substituent group g-2, a pyrrolyl group that may optionally have one substituent selected from the following substituent group g-1 and substituent group g-2, or a phenyl group that may optionally have one substituent selected from the following substituent group g-1 and substituent group g-2:
[Substituent Group g-1]
C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl C1-6 alkyl group, phenyl C1-6 alkyl group, furyl C1-6 alkyl group, thienyl C1-6 alkyl group, benzofuryl C1-6 alkyl group, benzothienyl C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, phenoxy group, C3-8 cycloalkyl C1-6 alkoxy group, phenyl C1-6 alkoxy group, furyl C1-6 alkoxy group, thienyl C1-6 alkoxy group, pyridyl C1-6 alkoxy group, phenoxy C1-6 alkyl group and pyridyloxy C1-6 alkyl group; and
[Substituent Group g-2]
C1-6 alkyl group, C2-6 alkenyl group, C2-6 alkynyl group, C3-8 cycloalkyl C1-6 alkyl group, phenyl C1-6 alkyl group, furyl C1-6 alkyl group, thienyl C1-6 alkyl group, benzofuryl C1-6 alkyl group, benzothienyl C1-6 alkyl group, C1-6 alkoxy group, C3-6 alkenyloxy group, C3-6 alkynyloxy group, phenoxy group, C3-8 cycloalkyl C1-6 alkoxy group, phenyl C1-6 alkoxy group, furyl C1-6 alkoxy group, thienyl C1-6 alkoxy group, pyridyl C1-6 alkoxy group, phenoxy C1-6 alkyl group and pyridyloxy C1-6 alkyl group;
wherein each group described in the substituent group g-2 has one to three substituents selected from the following substituent group h:
halogen atom, hydroxyl group, cyano group, trifluoromethyl group, C1-6 alkyl group, C1-6 alkoxy group and C1-6 alkylthio group.
Still further preferably, such E may be a group, wherein one or two hydrogen atoms of any one of a 2-furyl group, a 2-thienyl group, a pyrrolyl group, and a phenyl group may be substituted with (more preferably, may be monosubstituted with) [a fluorine atom, a chlorine atom, a C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups or C1-6 alkyl groups), a C2-6 alkenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups or C1-6 alkyl groups), a C2-6 alkynyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, or C1-6 alkyl groups), a C3-5 cycloalkyl C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-5 cycloalkylidene C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a phenyl C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenyl C2-6 alkenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a 5- or 6-membered heterocyclic C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups or C1-6 alkyl groups), a C1-6 alkoxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-6 alkenyloxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-6 alkynyloxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a phenoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups or C1-6 alkyl groups), a C3-6 cycloalkyl C1-6 alkoxy group optionally substituted with one to three halogen atoms, a phenyl C1-6 alkoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a 5- or 6-membered heterocyclic C1-6 alkoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenoxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, or 5- or 6-membered heterocyclic oxy groups) or a 5- or 6-membered heterocyclic oxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, or C1-6 alkoxy groups).
Particularly preferably, such E may be a group, wherein one or two hydrogen atoms of any one of a 2-furyl group, a 2-thienyl group, and a phenyl group may be substituted with (more preferably, may be monosubstituted with) [a fluorine atom, a chlorine atom, a C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups or C1-6 alkyl groups), a C2-6 alkenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a C2-6 alkynyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, or C1-6 alkyl groups), a C3-5 cycloalkyl C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-5 cycloalkylidene C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a phenyl C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenyl C2-6 alkenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a 5- or 6-membered heterocyclic C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a C1-6 alkoxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-6 alkenyloxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-6 alkynyloxy group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a phenoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a C3-6 cycloalkyl C1-6 alkoxy group optionally substituted with one to three halogen atoms, a phenyl C1-6 alkoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a 5- or 6-membered heterocyclic C1-6 alkoxy group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenoxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, or 5- or 6-membered heterocyclic oxy groups), or a 5- or 6-membered heterocyclic oxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, or C1-6 alkoxy groups)]; or
a 3-pyrrolyl group whose N (nitrogen atom) may be substituted with [a C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a C2-6 alkenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a C2-6 alkynyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, or C1-6 alkyl groups), a C3-5 cycloalkyl C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a C3-5 cycloalkylidene C1-6 alkyl group (optionally substituted with one to three halogen atoms or C1-6 alkyl groups), a phenyl C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a 5- or 6-membered heterocyclic C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, 5- or 6-membered heterocyclic oxy groups, or C1-6 alkyl groups), a phenoxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, C1-6 alkoxy groups, phenoxy groups, or 5- or 6-membered heterocyclic oxy groups), or a 5- or 6-membered heterocyclic oxy C1-6 alkyl group (optionally substituted with one to three halogen atoms, C3-5 cycloalkyl groups, or C1-6 alkoxy groups)].
In the present specification, examples of a halogen atom may include a fluorine atom, a chlorine atom, and a bromine atom. Examples of a C1-6 alkyl group may include a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, an n-pentyl group, an iso-pentyl group, an n-hexyl group, a 4-methylpentyl group, and a 3-methylpentyl group. Examples of a C2-6 alkenyl group may include a vinyl group, an allyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, a 3-pentenyl group, a prenyl group, a 3-methyl-3-butenyl group, a 2-hexenyl group, a 3-hexenyl group, a 4-hexenyl group, a 4-methyl-4-pentenyl group, and a 4-methyl-3-pentenyl group. Examples of a C2-6 alkynyl group may include an ethynyl group, a propargyl group, a 2-butyryl group, a 3-butyryl group, a 2-pentynyl group, a 3-pentynyl group, a 4-pentynyl group, a 2-hexynyl group, a 3-hexynyl group, a 4-hexynyl group, and a 5-hexynyl group. Examples of a C3-8 cycloalkyl group may include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group. Examples of a C6-10 aryl group may include a phenyl group, an indennyl group, and a naphthyl group. Examples of a 5- to 10-membered heterocyclic group may include a furyl group, a thienyl group, a thiazolyl group, a pyrazolyl group, a pyridyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a benzofuranyl group, a benzothienyl group, a benzothiazolyl group, a chromenyl group, an isocromenyl group, a thiocromenyl group, and an isothiocromenyl group. Examples of a C3-8 cycloalkyl C1-6 alkyl group may include a cyclopropylmethyl group, a cyclopropylethyl group, a cyclopropylpropyl group, a cyclopropylbutyl group, a cyclopropylpentyl group, a cyclopropylhexyl group, a cyclobutylmethyl group, a cyclobutylethyl group, a cyclobutylpropyl group, a cyclobutylbutyl group, a cyclobutylpentyl group, a cyclopentylethyl group, a cyclopentylpropyl group, a cyclopentylbutyl group, a cyclohexylethyl group, and a cyclohexylpropyl group. Examples of a C3-8 cycloalkylidene C1-6 alkyl group may include a cyclopropylidenemethyl group, a cyclopropylideneethyl group, a cyclopropylidenepropyl group, a cyclopropylidenebutyl group, a cyclopropylidenepentyl group, a cyclopropylidenehexyl group, a cyclobutylidenemethyl group, a cyclobutylideneethyl group, a cyclobutylidenepropyl group, a cyclobutylidenebutyl group, a cyclobutylidenepentyl group, a cyclopentylideneethyl group, a cyclopentylidenepropyl group, a cyclopentylidenebutyl group, a cyclohexylideneethyl group, and a cyclohexylidenepropyl group. Examples of a C6-10 aryl C1-6 alkyl group may include a benzyl group, a phenethyl group, a phenylpropyl group, a phenylbutyl group, a phenylpentyl group, a 2-methyl-4-phenylbutyl group, a 2-methyl-5-phenylpentyl group, a 3-methyl-5-phenylpentyl group, and a (2-naphthyl)ethyl group. Examples of a 5- to 10-membered heterocyclic C1-6 alkyl group may include a furylmethyl group, a furylethyl group, a furylpropyl group, a furylbutyl group, a furylpentyl group, a furylhexyl group, a thienylmethyl group, a thienylethyl group, a thienylpropyl group, a thienylbutyl group, a thienylpentyl group, and a thienylhexyl group. Examples of a C1-6 alkoxy group may include a methoxy group, an ethoxy group, an n-propyloxy group, an iso-propoxy group, an n-butoxy group, an iso-butoxy group, a sec-butoxy group, an n-pentyloxy group, an iso-pentyloxy group, a sec-pentyloxy group, an n-hexyloxy group, an iso-hexyloxy group, a sec-hexyloxy group, and a 2,3-dimethylbutoxy group. Examples of a C3-6 alkenyloxy group may include an allyloxy group, a 1-methyl-2-propenyloxy group a 2-butenyloxy group, a 3-butenyloxy group, a 2-pentenyloxy group, a 3-pentenyloxy group, a prenyloxy group, a 3-methyl-3-butenyloxy group, a 2-hexenyloxy group, a 3-hexenyloxy group, a 4-hexenyloxy group, a 4-methyl-4-pentenyloxy group, and a 4-methyl-3-pentenyloxy group. Examples of a C3-6 alkynyloxy group may include a propargyloxy group, a 2-butynyloxy group, a 3-butynyloxy group, a 2-pentynyloxy group, a 3-pentynyloxy group, a 4-pentynyloxy group, a 2-hexynyloxy group, a 3-hexynyloxy group, a 4-hexynyloxy group, and a 5-hexynyloxy group. Examples of a C3-8 cycloalkoxy group may include a cyclopropyloxy group, a cyclobutyloxy group, a cyclopentyloxy group, a cyclohexyloxy group, a cycloheptyloxy group, and a cyclooctyloxy group. Examples of a C6-10 aryloxy group may include a phenoxy group and a naphthoxy group. Examples of a C3-8 cycloalkyl C1-6 alkoxy group may include a cyclopropylmethoxy group, a cyclopropylethoxy group, a cyclopropylpropoxy group, a cyclopropylbutoxy group, a cyclopropylpentyloxy group, a cyclopropylhexyloxy group, a cyclobutylmethoxy group, a cyclobutylethoxy group, a cyclobutylpropoxy group, a cyclobutylbutoxy group, a cyclobutylpentyloxy group, a cyclopentylethoxy group, a cyclopentylpropoxy group, a cyclopentylbutoxy group, a cyclohexylethoxy group, and a cyclohexylpropoxy group. Examples of a C6-10 aryl C1-6 alkoxy group may include a benzyloxy group, a phenethyloxy group, a phenylpropyloxy group, a phenylbutyloxy group, a phenylpentyloxy group, a 2-methyl-4-phenylbutyloxy group, a 2-methyl-5-phenylpentyloxy group, a 3-methyl-5-phenylpentyloxy group and a (2-naphthyl)ethyloxy group. Examples of a 5- to 10-membered heterocyclic C1-6 alkoxy group may include a furylmethoxy group, a furylethoxy group, a furylpropyloxy group, a furylbutyloxy group, a furylpentyloxy group, a furylhexyloxy group, a thienylmethoxy group, a thienylethoxy group, a thienylpropyloxy group, a thienylbutyloxy group, a thienylpentyloxy group, and a thienylhexyloxy group. Examples of a C1-6 alkylthio group may include a methylthio group, an ethylthio group, an n-propylthio group, an iso-propylthio group, an n-butylthio group, an iso-butylthio group, an n-penylthio group, an iso-pentylthio group, an n-hexylthio group, a 4-methylpentylthio group, and a 3-methylpentylthio group. Examples of a C3-6 alkenylthio group may include an allylthio group, a 1-methyl-2-propenylthio group, a 2-butenylthio group, a 3-butenylthio group, a 2-pentenylthio group, a 3-pentenylthio group, a prenylthio group, a 3-methyl-3-butenylthio group, a 2-hexenylthio group, a 3-hexenylthio group, a 4-hexenylthio group, a 4-methyl-4-pentenylthio group and a 4-methyl-3-pentenylthio group. Examples of a C3-6 alkynylthio group may include a propargylthio group, a 2-butynylthio group, a 3-butynylthio group, a 2-pentynylthio group, a 3-pentynylthio group, a 4-pentynylthio group, a 2-hexynylthio group, a 3-hexynylthio group, a 4-hexynylthio group, and a 5-hexynylthio group. Examples of a C3-8 cycloalkylthio group may include a cyclopropylthio group, a cyclobutylthio group, a cyclopentylthio group, a cyclohexylthio group, a cycloheptylthio group, and a cyclooctylthio group. Examples of a C6-10 arylthio group may include phenylthio group and naphthylthio group. Examples of a C3-8 cycloalkyl C1-6 alkylthio group may include a cyclopropylmethylthio group, a cyclopropylethylthio group, a cyclopropylpropylthio group, a cyclopropylbutylthio group, a cyclopropylpentylthio group, a cyclopropylhexylthio group, a cyclobutylmethylthio group, a cyclobutylethylthio group, a cyclobutylpropylthio group, a cyclobutylbutylthio group, a cyclobutylpentylthio group, a cyclopentylethylthio group, a cyclopentylpropylthio group, a cyclopentylbutylthio group, a cyclohexylethylthio group, and a cyclohexylpropylthio group. Examples of a C6-10 aryl C1-6 alkylthio group may include a benzylthio group, a phenethylthio group, a phenylpropylthio group, a phenylbutylthio group, a phenylpentylthio group, a 2-methyl-4-phenylbutylthio group, a 2-methyl-5-phenylpentylthio group, and a 3-methyl-5-phenylpentylthio group. Examples of a 5- to 10-membered heterocyclic C1-6 alkylthio group may include a furylmethylthio group, a furylethylthio group, a furylpropylthio group, a furylbutylthio group, a furylpentylthio group, a furylhexylthio group, a thienylethylthio group, a thienylmethylthio group, a thienylpropylthio group, a thienylbutylthio group, a thienylpentylthio group, and a thienylhexylthio group. Examples of a mono-C1-6 alkylamino group may include a methylamino group, an ethylamino group, an n-propylamino group, an iso-propylamino group, an n-butylamino group, an iso-butylamino group, an n-pentylamino group, an iso-pentylamino group, an n-hexylamino group, a 4-methylpentylamino group, and a 3-methylpentylamino group. Examples of a mono-C3-6 alkenylamino group may include an allylamino group, a 2-butenylamino group, a 3-butenylamino group, a 2-pentenylamino group, a 3-pentenylamino group, a prenylamino group, a 3-methyl-3-butenylamino group, a 2-hexenylamino group, a 3-hexenylamino group, a 4-hexenylamino group, a 4-methyl-4-pentenylamino group and a 4-methyl-3-pentenylamino group. Examples of a mono-C3-6 alkynylamino group may include a propargylamino group, a 2-butynylamino group, a 3-butynyl group amino, a 2-pentynylamino group, a 3-pentynylamino group, a 4-pentynylamino group, a 2-hexynylamino group, a 3-hexynylamino group, a 4-hexynylamino group, and a 5-hexynylamino group. Examples of a mono-C3-8 cycloalkylamino group may include a cyclopropylamino group, a cyclobutylamino group, a cyclopentylamino group, a cyclohexylamino group, a cycloheptylamino group, and a cyclooctylamino group. Examples of a mono-C6-10 arylamino group may include a phenylamino group and a naphthylamino group. Examples of a mono-C3-8 cycloalkyl C1-6 alkylamino group may include a cyclopropylmethylamino group, a cyclopropylethylamino group, a cyclopropylpropylamino group, a cyclopropylbutylamino group, a cyclopropylpentylamino group, a cyclopropylhexylamino group, a cyclobutylmethylamino group, a cyclobutylethylamino group, a cyclobutylpropylamino group, a cyclobutylbutylamino group, a cyclobutylpentylamino group, a cyclopentylethylamino group, a cyclopentylpropylamino group, a cyclopentylbutylamino group, a cyclohexylethylamino group, and a cyclohexylpropylamino group. Examples of a mono-C6-10 aryl C1-6 alkylamino group may include a benzylamino group, a phenethylamino group, a phenylpropylamino group, a phenylbutylamino group, a phenylpentylamino group, a 2-methyl-4-phenylbutylamino group, a 2-methyl-5-phenylpentylamino group, a 3-methyl-5-phenylpentylamino group and a (2-naphthyl)ethylamino group. Examples of a mono-5- to 10-membered heterocyclic C1-6 alkylamino group may include a furylmethylamino group, a furylethylamino group, a furylpropylamino group, a furylbutylamino group, a furylpentylamino group, a furylhexylamino group, a thienylethylamino group, a thienylmethylamino group, a thienylpropylamino group, a thienylbutylamino group, a thienylpentylamino group and a thienylhexylamino group. Examples of a di-C1-6 alkylamino group may include a dimethylamino group, a methylethylamino group, a diethylamino group, a methylpropylamino group, and a methylbutylamino group. Examples of an N—C3-6 alkenyl-N—C1-6 alkylamino group may include an N-allyl-N-methylamino group, an N-(2-butenyl)-N-methylamino group, and an N-(3-butenyl)-N-methylamino group. Examples of an N—C3-6 alkynyl-N—C1-6 alkylamino group may include an N-methyl-N-propargylamino group, an N-(2-butynyl)-N-methylamino group, and an N-(3-butynyl)-N-methylamino group. Examples of an N—C3-8 cycloalkyl-N—C1-6 alkylamino group may include an N-cyclopropyl-N-methylamino group, an N-cyclobutyl-N-methylamino group, and an N-cyclopentyl-N-methylamino group. An example of an N—C6-10 aryl-N—C1-6 alkylamino group may include an N-methylanilino group. Examples of an N—C3-8 cycloalkyl C1-6 alkyl-N—C1-6 alkylamino group may include an N-cyclopropylmethyl-N-methylamino group, an N-cyclopropylethyl-N-methylamino group, an N-cyclopropylpropyl-N-methylamino group, an N-cyclobutylmethyl-N-methylamino group, an N-cyclobutylethyl-N-methylamino group and an N-cyclobutylpropyl-N-methylamino group. Examples of an N—C6-10 aryl C1-6 alkyl-N—C1-6 alkylamino group may include an N-benzyl-N-methylamino group, an N-phenethyl-N-methylamino group, an N-phenylpropyl-N-methylamino group, an N-phenylbutyl-N-methylamino group, and an N-phenylpentyl-N-methylamino group. Examples of an N-5- to 10-membered heterocyclic C1-6 heterocyclic C1-6 alkyl-N—C1-6 alkylamino group may include an N-furylmethyl-N-methylamino group, an N-furylethyl-N-methylamino group, an N-furylpropyl-N-methylamino group, an N-furylbutyl-N-methylamino group, an N-furylpentyl-N-methylamino group, an N-thienyl-N-methylamino group, an N-thienylethyl-N-methylamino group, an N-thienylpropyl-N-methylamino group, an N-thienylbutyl-N-methylamino group and an N-thienylpentyl-N-methylamino group. Examples of a C1-6 alkoxycarbonyl group may include a methoxycarbonyl group, an ethoxycarbonyl group, an n-propyloxycarbonyl group, an iso-propoxycarbonyl group, an n-butoxycarbonyl group, an iso-butoxycarbonyl group, a sec-butoxycarbonyl group, an n-pentyloxycarbonyl group, an iso-pentyloxycarbonyl group, a sec-pentyloxycarbonyl group, an n-hexyloxycarbonyl group, an iso-hexyloxycarbonyl group and a sec-hexyloxycarbonyl group. Examples of a C1-6 alkylsulfonyl group may include a methanesulfonyl group, an ethanesulfonyl group, a propanesulfonyl group, a butanesulfonyl group, a pentanesulfonyl group, and a hexanesulfonyl group. Examples of a group represented by a formula —C(═N—Ra1)Ra2 may include a hydroxyiminomethyl group, a hydroxyiminoethyl group, a methoxyiminomethyl group, an ethoxyiminomethyl group, and a methoxyiminoethyl group. Examples of a C6-10 aryloxy C1-6 alkyl group may include a benzyloxymethyl group, a benzyloxyethyl group, a benzyloxypropyl group, a benzyloxybutyl group, a benzyloxypentyl group, and a (2-naphthyl)oxymethyl group. Examples of a 5- to 10-membered heterocyclic oxy C1-6 alkyl group may include a furyloxymethyl group, a furyloxyethyl group, a furyloxypropyl group, a furyloxybutyl group, a furyloxypentyl group, a thienyloxymethyl group, a thienyloxyethyl group, a thienyloxypropyl group, a thienyloxybutyl group, a thienyloxypentyl group, a pyridyloxymethyl group, a pyridyloxyethyl group, a benzofuranyloxymethyl group, and a benzothienyloxymethyl group. Examples of a C6-10 aryl C2-6 alkenyl group may include a styryl group and a phenylpropenyl group.
More specific examples of such E may include a phenyl group, a 2-furyl group, a 3-furyl group, a 2-thienyl group, a 3-thienyl group, a 5-phenylfuran-2-yl group, a 5-phenoxyfuran-2-yl group, a 5-(4-fluorophenoxy)furan-2-yl group, a 5-(3-fluorophenoxy)furan-2-yl group, a 5-(4-methylphenoxy)furan-2-yl group, a 5-(4-chlorophenoxy)furan-2-yl group, a 5-(3-chlorophenoxy)furan-2-yl group, a 5-(3-methylphenoxy)furan-2-yl group, a 544-methoxyphenoxy)furan-2-yl group, a 5-(3-methoxyphenoxy)furan-2-yl group, a 5-benzylfuran-2-yl group, a 5-(4-fluorophenyl)methylfuran-2-yl group, a 5-(3-fluorophenyl)methylfuran-2-yl group, a 5-(4-methylphenyl)methylfuran-2-yl group, a 5-(4-chlorophenyl)methylfuran-2-yl group, a 5-(3-chlorophenyl)methylfuran-2-yl group, a 5-(3-methylphenyl)methylfuran-2-yl group, a 5-(4-methoxyphenyl)methylfuran-2-yl group, a 5-(3-methoxyphenyl)methylfuran-2-yl group, a 5-phenoxythiophen-2-yl group, a 5-(4-fluorophenoxy)thiophen-2-yl group, a 5-(3-fluorophenoxy)thiophen-2-yl group, a 5-(2-fluorophenoxy)thiophen-2-yl group, a 5-(4-methylphenoxy)thiophen-2-yl group, a 5-(4-chlorophenoxy)thiophen-2-yl group, a 5-(3-chlorophenoxy)thiophen-2-yl group, a 5-(3-methylphenoxy)thiophen-2-yl group, a 5-(4-methoxyphenoxy)thiophen-2-yl group, a 5-(3-methoxyphenoxy)thiophen-2-yl group, a 5-(3-cyanophenoxy)thiophen-2-yl group, a 5-benzyloxythiophen-2-yl group, a 5-benzylthiophen-2-yl group, a 5-(4-fluorophenyl)methylthiophen-2-yl group, a 5-(3-fluorophenyl)methylthiophen-2-yl group, a 5-(4-methylphenyl)methylthiophen-2-yl group, a 5-(4-chlorophenyl)methylthiophen-2-yl group, a 5-(3-chlorophenyl)methylthiophen-2-yl group, a 5-(3-methylphenyl)methylthiophen-2-yl group, a 5-(4-methoxyphenyl)methylthiophen-2-yl group, a 5-(3-methoxyphenyl)methylthiophen-2-yl group, a 5-(2-thienyl)methylthiophen-2-yl group, a 5-(2-pyridyl)methylthiophen-2-yl group, a 5-(2-benzofuranyl)methylthiophen-2-yl group, a 5-phenoxythiophen-3-yl group, a 5-(4-fluorophenoxy)thiophen-3-yl group, a 5-(3-fluorophenoxy)thiophen-3-yl group, a 5-(4-methylphenoxy)thiophen-3-yl group, a 5-(4-chlorophenoxy)thiophen-3-yl group, a 5-(3-chlorophenoxy)thiophen-3-yl group, a 5-(3-methylphenoxy)thiophen-3-yl group, a 5-(4-methoxyphenoxy)thiophen-3-yl group, a 5-(3-methoxyphenoxy)thiophen-3-yl group, a 3-methylphenyl group, a 3-ethylphenyl group, a 3-propylphenyl group, a 3-butylphenyl group, a 3-pentylphenyl group, a 3-hexylphenyl group, a 3-heptylphenyl group, a 3-isobutylphenyl group, a 3-(2-isobutenyl)phenyl group, a 3-cyclopentylmethylidenephenyl group, a 3-biphenylyl group, 3-benzylphenyl group, a 3-phenylaminophenyl group, a 3-(N-phenyl-N-methylamino)phenyl group, a 3-phenylthiophenyl group, a 3-phenoxyphenyl group, a 3-(2-fluorophenoxy)phenyl group, a 3-(3-fluorophenoxy)phenyl group, a 3-(4-fluorophenoxy)phenyl group, a 3-(3,5-difluorophenoxy)phenyl group, a 3-(2-chlorophenoxy)phenyl group, a 3-(3-chlorophenoxy)phenyl group, a 3-(4-chlorophenoxy)phenyl group, a 3-(2-methylphenoxy)phenyl group, a 3-(3-methylphenoxy)phenyl group, a 3-(4-methylphenoxy)phenyl group, a 3-(2-methoxyphenoxy)phenyl group, a 3-(3-methoxyphenoxy)phenyl group, a 3-(4-methoxyphenoxy)phenyl group, a 3-(2-cyanophenoxy)phenyl group, a 3-(3-cyanophenoxy)phenyl group, a 3-(4-cyanophenoxy)phenyl group, a 3-benzyloxyphenyl group, a 3-(2-fluorophenylmethoxy)phenyl group, a 3-(3-fluorophenylmethoxy)phenyl group, a 3-(4-fluorophenylmethoxy)phenyl group, a 3-(3,5-difluorophenylmethoxy)phenyl group, a 3-(2-chlorophenylmethoxy)phenyl group, a 3-(3-chlorophenylmethoxy)phenyl group, a 3-(4-chlorophenylmethoxy)phenyl group, a 3-(2-methylphenylmethoxy)phenyl group, a 3-(3-methylphenylmethoxy)phenyl group, a 3-(4-methylphenylmethoxy)phenyl group, a 3-(2-methoxyphenylmethoxy)phenyl group, a 3-(3-methoxyphenylmethoxy)phenyl group, a 3-(4-methoxyphenylmethoxy)phenyl group, a 3-(2-cyanophenylmethoxy)phenyl group, a 3-(3-cyanophenylmethoxy)phenyl group, a 3-(4-cyanophenylmethoxy)phenyl group, a 3-benzylaminophenyl group, a 3-(N-benzyl-N-methylamino)phenyl group, a 3-(2-furylmethoxy)phenyl group, a 3-(3-furylmethoxy)phenyl group, a 3-(2-thienylmethoxy)phenyl group, 3-(3-thienylmethoxy)phenyl group, a 3-(2-pyridylmethoxy)phenyl group, a 3-(3-pyridylmethoxy)phenyl group, a 3-(4-pyridylmethoxy)phenyl group, a 3-(2-pyridyloxy)phenyl group, a 3-(3-pyridyloxy)phenyl group, a 3-(4-pyridyloxy)phenyl group, a 3-(6-trifluoromethylpyridin-2-yloxy)phenyl group, a 3-(5-trifluoromethylpyridin-2-yloxy)phenyl group, a 3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl group, a 3-(2-pyrazinyloxy)phenyl group, a 3-(6-chloropyridazin-3-yloxy)phenyl group, a 3-methoxyphenyl group, a 3-ethoxyphenyl group, a 3-propoxyphenyl group, a 3-(2-methylethoxy)phenyl group, a 3-butoxyphenyl group, a 3-(2-methylbutoxy)phenyl group, a 3-(3-methylbutoxy)phenyl group, a 3-pentyloxyphenyl group, a 3-hexyloxyphenyl group, a 3-heptyloxyphenyl group, a 3-isoprenyloxyphenyl group, a 3-(2-fluoroethoxy)phenyl group, a 3-(3-fluoropropoxy)phenyl group, a 3-(4-fluorobutoxy)phenyl group, a 3-(5-fluoropentyloxy)phenyl group, a 3-(6-fluorohexyloxy)phenyl group, a 3-(7-fluoroheptyloxy)phenyl group, a 3-(2-chloroethoxy)phenyl group, a 3-(3-chloropropoxy)phenyl group, a 3-(4-chlorobutoxy)phenyl group, a 3-(5-chloropentyloxy)phenyl group, a 3-(6-chlorohexyloxy)phenyl group, a 3-(7-chloroheptyloxy)phenyl group, a 3-(2-propenyoxy)phenyl group, a 3-(2-butenyloxy)phenyl group, a 3-(3-butenyloxy)phenyl group, a 3-(2-pentenyloxy)phenyl group, a 3-(3-pentenyloxy)phenyl group, a 3-(4-pentenyloxy)phenyl group, a 3-(2-hexenyloxy)phenyl group, a 3-(3-hexenyloxy)phenyl group, a 3-(4-hexenyloxy)phenyl group, a 3-(5-hexenyloxy)phenyl group, a 3-(2-heptenyloxy)phenyl group, a 3-(3-heptenyloxy)phenyl group, a 3-(4-heptenyloxy)phenyl group, a 3-(5-heptenyloxy)phenyl group, a 3-(6-heptenyloxy)phenyl group, a 3-(3-chloro-2-propenyloxy)phenyl group, a 3-(3,3-dichloro-2-propenyloxy)phenyl group, a 3-(2-methyl-2-butenyloxy)phenyl group, a 3-(3-methyl-2-butenyloxy)phenyl group, a 3-(2-propynyloxy)phenyl group, a 3-(2-butynyloxy)phenyl group, a 3-(3-butynyloxy)phenyl group, a 3-(2-pentynyloxy)phenyl group, a 3-(3-pentynyloxy)phenyl group, a 3-(4-pentynyloxy)phenyl group, a 3-(2-hexynyloxy)phenyl group, a 3-(3-hexynyloxy)phenyl group, a 3-(4-hexynyloxy)phenyl group, a 3-(5-hexynyloxy)phenyl group, a 3-(2-heptynyloxy)phenyl group, a 3-(3-heptynyloxy)phenyl group, a 3-(4-heptynyloxy)phenyl group, a 3-(5-heptynyloxy)phenyl group, a 3-(6-heptynyloxy)phenyl group, a 3-(2-methoxyethoxy)phenyl group, a 3-(3-methoxypropoxy)phenyl group, a 3-(4-methoxybutoxy)phenyl group, a 345-methoxypentyloxy)phenyl group, a 3-(6-methoxyhexyloxy)phenyl group, a 3-(7-methoxyheptyloxy)phenyl group, a 3-(2-ethoxyethoxy)phenyl group, a 3-(3-ethoxypropoxy)phenyl group, a 3-(4-ethoxybutoxy)phenyl group, a 345-ethoxypentyloxy)phenyl group, a 3-(6-ethoxyhexyloxy)phenyl group, a 3-(7-ethoxyheptyloxy)phenyl group, a 3-cyclopropylmethoxyphenyl group, a 3-(2-cyclopropylethoxy)phenyl group, a 3-(3-cyclopropylpropoxy)phenyl group, a 3-(4-cyclopropylbutoxy)phenyl group, a 3-(5-cyclopropylpentyloxy)phenyl group, a 3-(6-cyclopropylhexyloxy)phenyl group, a 3-(7-cyclopropylheptyloxy)phenyl group, a 3-phenoxymethylphenyl group, a 3-(2-phenylethyl)phenyl group, a 3-(3-phenylpropyl)phenyl group, a 3-(4-phenylbutyl)phenyl group, a 3-(5-phenylpentyl)phenyl group, a 3-(2-phenylethoxy)phenyl group, a 3-(3-phenylpropoxy)phenyl group, a 3-(4-phenylbutoxy)phenyl group, a 3-(5-phenylpentyloxy)phenyl group, a (Z)-3-styrylphenyl group, a 2-fluoro-3-methylphenyl group, a 2-fluoro-3-ethylphenyl group, a 2-fluoro-3-propylphenyl group, a 2-fluoro-3-butylphenyl group, a 2-fluoro-3-pentylphenyl group, a 2-fluoro-3-hexylphenyl group, a 2-fluoro-3-heptylphenyl group, a 2-fluoro-3-isobutylphenyl group, a 2-fluoro-3-(2-isobutenyl)phenyl group, a 2-fluoro-3-cyclopentylmethylidenephenyl group, a 2-fluoro-3-biphenylyl group, a 2-fluoro-3-benzylphenyl group, a 2-fluoro-3-phenylaminophenyl group, a 2-fluoro-3-(N-phenyl-N-methylamino)phenyl group, a 2-fluoro-3-phenylthiophenyl group, a 2-fluoro-3-phenoxyphenyl group, a 2-fluoro-3-(2-fluorophenoxy)phenyl group, a 2-fluoro-3-(3-fluorophenoxy)phenyl group, a 2-fluoro-3-(4-fluorophenoxy)phenyl group, a 2-fluoro-3-(3,5-difluorophenoxy)phenyl group, a 2-fluoro-3-(2-chlorophenoxy)phenyl group, a 2-fluoro-3-(3-chlorophenoxy)phenyl group, a 2-fluoro-3-(4-chlorophenoxy)phenyl group, a 2-fluoro-3-(2-methylphenoxy)phenyl group, a 2-fluoro-3-(3-methylphenoxy)phenyl group, a 2-fluoro-3-(4-methylphenoxy)phenyl group, a 2-fluoro-3-(2-methoxyphenoxy)phenyl group, a 2-fluoro-3-(3-methoxyphenoxy)phenyl group, a 2-fluoro-3-(4-methoxyphenoxy)phenyl group, a 2-fluoro-3-(2-cyanophenoxy)phenyl group, a 2-fluoro-3-(3-cyanophenoxy)phenyl group, a 2-fluoro-3-(4-cyanophenoxy)phenyl group, a 3-benzyloxyphenyl group, a 2-fluoro-3-(2-fluorophenylmethoxy)phenyl group, a 2-fluoro-3-(3-fluorophenylmethoxy)phenyl group, a 2-fluoro-3-(4-fluorophenylmethoxy)phenyl group, a 2-fluoro-3-(3,5-difluorophenylmethoxy)phenyl group, a 2-fluoro-3-(2-chlorophenylmethoxy)phenyl group, a 2-fluoro-3-(3-chlorophenylmethoxy)phenyl group, a 2-fluoro-3-(4-chlorophenylmethoxy)phenyl group, a 2-fluoro-3-(2-methylphenylmethoxy)phenyl group, a 2-fluoro-3-(3-methylphenylmethoxy)phenyl group, a 2-fluoro-3-(4-methylphenylmethoxy)phenyl group, a 2-fluoro-3-(2-methoxyphenylmethoxy)phenyl group, a 2-fluoro-3-(3-methoxyphenylmethoxy)phenyl group, a 2-fluoro-3-(4-methoxyphenylmethoxy)phenyl group, a 2-fluoro-3-(2-cyanophenylmethoxy)phenyl group, a 2-fluoro-3-(3-cyanophenylmethoxy)phenyl group, a 2-fluoro-3-(4-cyanophenylmethoxy)phenyl group, a 2-fluoro-3-benzylaminophenyl group, a 2-fluoro-3-(N-benzyl-N-methylamino)phenyl group, a 2-fluoro-3-(2-furylmethoxy)phenyl group, a 2-fluoro-3-(3-furylmethoxy)phenyl group, a 2-fluoro-3-(2-thienylmethoxy)phenyl group, a 2-fluoro-3-(3-thienylmethoxy)phenyl group, a 2-fluoro-3-(2-pyridylmethoxy)phenyl group, a 2-fluoro-3-(3-pyridylmethoxy)phenyl group, a 2-fluoro-3-(4-pyridylmethoxy)phenyl group, a 2-fluoro-3-(2-pyridyloxy)phenyl group, a 2-fluoro-3-(3-pyridyloxy)phenyl group, a 2-fluoro-3-(4-pyridyloxy)phenyl group, a 2-fluoro-3-(6-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-3-(5-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-3-(2-pyrazinyloxy)phenyl group, a 2-fluoro-3-(6-chloropyridazin-3-yloxy)phenyl group, a 2-fluoro-3-methoxyphenyl group, a 2-fluoro-3-ethoxyphenyl group, a 2-fluoro-3-propoxyphenyl group, a 2-fluoro-3-(2-methylethoxy)phenyl group, a 2-fluoro-3-butoxyphenyl group, a 2-fluoro-3-(2-methylbutoxy)phenyl group, a 2-fluoro-3-(3-methylbutoxy)phenyl group, a 2-fluoro-3-pentyloxyphenyl group, a 2-fluoro-3-hexyloxyphenyl group, a 2-fluoro-3-heptyloxyphenyl group, a 2-fluoro-3-isoprenyloxyphenyl group, a 2-fluoro-3-(2-fluoroethoxy)phenyl group, a 2-fluoro-3-(3-fluoropropoxy)phenyl group, a 2-fluoro-3-(4-fluorobutoxy)phenyl group, a 2-fluoro-3-(5-fluoropentyloxy)phenyl group, a 2-fluoro-3-(6-fluorohexyloxy)phenyl group, a 2-fluoro-3-(7-fluoroheptyloxy)phenyl group, a 2-fluoro-3-(2-chloroethoxy)phenyl group, a 2-fluoro-3-(3-chloropropoxy)phenyl group, a 2-fluoro-3-(4-chlorobutoxy)phenyl group, a 2-fluoro-3-(5-chloropentyloxy)phenyl group, a 2-fluoro-3-(6-chlorohexyloxy)phenyl group, a 2-fluoro-(7-chloroheptyloxy)phenyl group, a 2-fluoro-3-(2-propenyloxy)phenyl group, a 2-fluoro-3-(2-butenyloxy)phenyl group, a 2-fluoro-3-(3-butenyloxy)phenyl group, a 2-fluoro-3-(2-pentenyloxy)phenyl group, a 2-fluoro-3-(3-pentenyloxy)phenyl group, a 2-fluoro-3-(4-pentenyloxy)phenyl group, a 2-fluoro-3-(2-hexenyloxy)phenyl group, a 2-fluoro-3-(3-hexenyloxy)phenyl group, a 2-fluoro-3-(4-hexenyloxy)phenyl group, a 2-fluoro-3-(5-hexenyloxy)phenyl group, a 2-fluoro-3-(2-heptenyloxy)phenyl group, a 2-fluoro-3-(3-heptenyloxy)phenyl group, a 2-fluoro-3-(4-heptenyloxy)phenyl group, a 2-fluoro-3-(5-heptenyloxy)phenyl group, a 2-fluoro-3-(6-heptenyloxy)phenyl group, a 2-fluoro-3-(3-chloro-2-propenyloxy)phenyl group, a 2-fluoro-3-(3,3-dichloro-2-propenyloxy)phenyl group, a 2-fluoro-3-(2-methyl-2-butenyloxy)phenyl group, a 2-fluoro-3-(3-methyl-2-butenyloxy)phenyl group, a 2-fluoro-3-(2-propynyloxy)phenyl group, a 2-fluoro-3-(2-butynyloxy)phenyl group, a 2-fluoro-3-(3-butynyloxy)phenyl group, a 2-fluoro-3-(2-pentynyloxy)phenyl group, a 2-fluoro-3-(3-pentynyloxy)phenyl group, a 2-fluoro-3-(4-pentynyloxy)phenyl group, a 2-fluoro-3-(2-hexynyloxy)phenyl group, a 2-fluoro-3-(3-hexynyloxy)phenyl group, a 2-fluoro-3-(4-hexynyloxy)phenyl group, a 2-fluoro-3-(5-hexynyloxy)phenyl group, a 2-fluoro-3-(2-heptynyloxy)phenyl group, a 2-fluoro-3-(3-heptynyloxy)phenyl group, a 2-fluoro-3-(4-heptynyloxy)phenyl group, a 2-fluoro-3-(5-heptynyloxy)phenyl group, a 2-fluoro-3-(6-heptynyloxy)phenyl group, a 3-(2-methoxyethoxy)phenyl group, a 2-fluoro-3-(3-methoxypropoxy)phenyl group, a 2-fluoro-3-(4-methoxybutoxy)phenyl group, a 2-fluoro-3-(5-methoxypentyloxy)phenyl group, a 2-fluoro-3-(6-methoxyhexyloxy)phenyl group, a 2-fluoro-3-(7-methoxyheptyloxy)phenyl group, a 2-fluoro-3-(2-ethoxyethoxy)phenyl group, a 2-fluoro-3-(3-ethoxypropoxy)phenyl group, a 2-fluoro-3-(4-ethoxybutoxy)phenyl group, a 2-fluoro-3-(5-ethoxypentyloxy)phenyl group, a 2-fluoro-3-(6-ethoxyhexyloxy)phenyl group, a 2-fluoro-3-(7-ethoxyheptyloxy)phenyl group, a 2-fluoro-3-cyclopropylmethoxyphenyl group, a 2-fluoro-3-(2-cyclopropylethoxy)phenyl group, a 2-fluoro-3-(3-cyclopropylpropoxy)phenyl group, a 2-fluoro-3-(4-cyclopropylbutoxy)phenyl group, a 2-fluoro-3-(5-cyclopropylpentyloxy)phenyl group, a 2-fluoro-3-(6-cyclopropylhexyloxy)phenyl group, a 2-fluoro-3-(7-cyclopropylheptyloxy)phenyl group, a 2-fluoro-3-phenoxymethylphenyl group, a 2-fluoro-3-(2-phenylethyl)phenyl group, a 2-fluoro-3-(3-phenylpropyl)phenyl group, a 2-fluoro-3-(4-phenylbutyl)phenyl group, a 2-fluoro-3-(5-phenylpentyl)phenyl group, a 2-fluoro-3-(2-phenylethoxy)phenyl group, a 2-fluoro-3-(3-phenylpropoxy)phenyl group, a 2-fluoro-3-(4-phenylbutoxy)phenyl group, a 2-fluoro-3-(5-phenylpentyloxy)phenyl group, a (Z)-2-fluoro-3-styrylphenyl group, a 4-methylphenyl group, a 4-ethylphenyl group, a 4-propylphenyl group, a 4-butylphenyl group, a 4-pentylphenyl group, a 4-hexylphenyl group, a 4-heptylphenyl group, a 4-isobutylphenyl group, a 4-(2-isobutenyl)phenyl group, a 4-cyclopentylmethylidenephenyl group, a 4-biphenylyl group, a 4-benzylphenyl group, a 4-phenylaminophenyl group, a 4-(N-phenyl-N-methylamino)phenyl group, a 4-phenylthiophenyl group, a 4-phenoxyphenyl group, a 4-(2-fluorophenoxy)phenyl group, a 4-(3-fluorophenoxy)phenyl group, a 4-(4-fluorophenoxy)phenyl group, a 4-(3,5-difluorophenoxy)phenyl group, a 4-(2-chlorophenoxy)phenyl group, a 4-(3-chlorophenoxy)phenyl group, a 4-(4-chlorophenoxy)phenyl group, a 4-(2-methylphenoxy)phenyl group, a 4-(3-methylphenoxy)phenyl group, a 4-(4-methylphenoxy)phenyl group, a 4-(2-methoxyphenoxy)phenyl group, a 4-(3-methoxyphenoxy)phenyl group, a 4-(4-methoxyphenoxy)phenyl group, a 4-(2-cyanophenoxy)phenyl group, a 4-(3-cyanophenoxy)phenyl group, a 4-(4-cyanophenoxy)phenyl group, a 4-benzyloxyphenyl group, a 4-(2-fluorophenylmethoxy)phenyl group, a 4-(3-fluorophenylmethoxy)phenyl group, a 4-(4-fluorophenylmethoxy)phenyl group, a 4-(3,5-difluorophenylmethoxy)phenyl group, a 4-(2-chlorophenylmethoxy)phenyl group, a 4-(3-chlorophenylmethoxy)phenyl group, a 4-(4-chlorophenylmethoxy)phenyl group, a 4-(2-methylphenylmethoxy)phenyl group, a 4-(3-methylphenylmethoxy)phenyl group, a 4-(4-methylphenylmethoxy)phenyl group, a 4-(2-methoxyphenylmethoxy)phenyl group, a 4-(3-methoxyphenylmethoxy)phenyl group, a 4-(4-methoxyphenylmethoxy)phenyl group, a 4-(2-cyanophenylmethoxy)phenyl group, a 4-(3-cyanophenylmethoxy)phenyl group, a 4-(4-cyanophenylmethoxy)phenyl group, a 4-benzylaminophenyl group, a 4-(N-benzyl-N-methylamino)phenyl group, a 4-(2-furylmethoxy)phenyl group, a 4-(3-furylmethoxy)phenyl group, a 4-(2-thienylmethoxy)phenyl group, a 4-(3-thienylmethoxy)phenyl group, a 4-(2-pyridylmethoxy)phenyl group, a 4-(3-pyridylmethoxy)phenyl group, a 4-(4-pyridylmethoxy)phenyl group, a 4-(2-pyridyloxy)phenyl group, a 4-(3-pyridyloxy)phenyl group, a 4-(4-pyridyloxy)phenyl group, a 4-(6-trifluoromethylpyridin-2-yloxy)phenyl group, a 4-(5-trifluoromethylpyridin-2-yloxy)phenyl group, a 4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl group, a 4-(2-pyrazinyloxy)phenyl group, a 4-(6-chloropyridazin-3-yloxy)phenyl group, a 4-methoxyphenyl group, a 4-ethoxyphenyl group, a 4-propoxyphenyl group, a 4-(2-methylethoxy)phenyl group, a 4-butoxyphenyl group, a 4-(2-methylbutoxy)phenyl group, a 4-(3-methylbutoxy)phenyl group, a 4-pentyloxyphenyl group, a 4-hexyloxyphenyl group, a 4-heptyloxyphenyl group, a 4-isoprenyloxyphenyl group, a 4-(2-fluoroethoxy)phenyl group, a 4-(3-fluoropropoxy)phenyl group, a 4-(4-fluorobutoxy)phenyl group, a 4-(5-fluoropentyloxy)phenyl group, a 4-(6-fluorohexyloxy)phenyl group, a 4-(7-fluoroheptyloxy)phenyl group, a 4-(2-chloroethoxy)phenyl group, a 4-(3-chloropropoxy)phenyl group, a 4-(4-chlorobutoxy)phenyl group, a 4-(5-chloropentyloxy)phenyl group, a 4-(6-chlorohexyloxy)phenyl group, a 4-(7-chloroheptyloxy)phenyl group, a 4-(2-propenyloxy)phenyl group, a 4-(2-butenyloxy)phenyl group, a 4-(3-butenyloxy)phenyl group, a 4-(2-pentenyloxy)phenyl group, a 4-(3-pentenyloxy)phenyl group, a 4-(4-pentenyloxy)phenyl group, a 4-(2-hexenyloxy)phenyl group, a 4-(3-hexenyloxy)phenyl group, a 4-(4-hexenyloxy)phenyl group, a 4-(5-hexenyloxy)phenyl group, a 4-(2-heptenyloxy)phenyl group, a 4-(3-heptenyloxy)phenyl group, a 4-(4-heptenyloxy)phenyl group, a 4-(5-heptenyloxy)phenyl group, a 4-(6-heptenyloxy)phenyl group, a 4-(3-chloro-2-propenyloxy)phenyl group, a 4-(3,3-dichloro-2-propenyloxy)phenyl group, a 4-(2-methyl-2-butenyloxy)phenyl group, a 4-(3-methyl-2-butenyloxy)phenyl group, a 4-(2-propynyloxy)phenyl group, a 4-(2-butynyloxy)phenyl group, a 4-(3-butynyloxy)phenyl group, a 4-(2-pentynyloxy)phenyl group, a 4-(3-pentynyloxy)phenyl group, a 4-(4-pentynyloxy)phenyl group, a 4-(2-hexynyloxy)phenyl group, a 4-(3-hexynyloxy)phenyl group, a 4-(4-hexynyloxy)phenyl group, a 4-(5-hexynyloxy)phenyl group, a 4-(2-heptynyloxy)phenyl group, a 4-(3-heptynyloxy)phenyl group, a 4-(4-heptynyloxy)phenyl group, a 4-(5-heptynyloxy)phenyl group, a 4-(6-heptynyloxy)phenyl group, a 4-(2-methoxyethoxy)phenyl group, a 4-(3-methoxypropoxy)phenyl group, a 4-(4-methoxybutoxy)phenyl group, a 4-(5-methoxypentyloxy)phenyl group, a 4-(6-methoxyhexyloxy)phenyl group, a 4-(7-methoxyheptyloxy)phenyl group, a 4-(2-ethoxyethoxy)phenyl group, a 4-(3-ethoxypropoxy)phenyl group, a 4-(4-ethoxybutoxy)phenyl group, a 4-(5-ethoxy pentyloxy)phenyl group, a 4-(6-ethoxyhexyloxy)phenyl group, a 4-(7-ethoxyheptyloxy)phenyl group, a 4-cyclopropylmethoxyphenyl group, a 4-(2-cyclopropylethoxy)phenyl group, a 4-(3-cyclopropylpropoxy)phenyl group, a 4-(4-cyclopropylbutoxy)phenyl group, a 4-(5-cyclopropylpentyloxy)phenyl group, a 4-(6-cyclopropylhexyloxy)phenyl group, a 4-(7-cyclopropylheptyloxy)phenyl group, a 4-phenoxymethylphenyl group, a 4-(2-phenylethyl)phenyl group, a 4-(3-phenylpropyl)phenyl group, a 4-(4-phenylbutyl)phenyl group, a 4-(5-phenylpentyl)phenyl group, a 4-(2-phenylethoxy)phenyl group, a 4-(3-phenylpropoxy)phenyl group, a 4-(4-phenylbutoxy)phenyl group, a 4-(5-phenylpentyloxy)phenyl group, a (Z)-4-styrylphenyl group, a 2-fluoro-4-methylphenyl group, a 2-fluoro-4-ethylphenyl group, a 2-fluoro-4-propylphenyl group, a 2-fluoro-4-butylphenyl group, a 2-fluoro-4-pentylphenyl group, a 2-fluoro-4-hexylphenyl group, a 2-fluoro-4-heptylphenyl group, a 2-fluoro-4-isobutylphenyl group, a 2-fluoro-4-(2-isobutenyl)phenyl group, a 2-fluoro-4-cyclopentylmethylidenephenyl group, a 2-fluoro-4-phenylphenyl group, a 2-fluoro-4-benzylphenyl group, a 2-fluoro-4-phenylaminophenyl group, a 2-fluoro-4-(N-phenyl-N-methylamino)phenyl group, a 2-fluoro-4-phenylthiophenyl group, a 2-fluoro-4-phenoxyphenyl group, a 2-fluoro-4-(2-fluorophenoxy)phenyl group, a 2-fluoro-4-(3-fluorophenoxy)phenyl group, a 2-fluoro-4-(4-fluorophenoxy)phenyl group, a 2-fluoro-4-(3,5-difluorophenoxy)phenyl group, a 2-fluoro-4-(2-chlorophenoxy)phenyl group, a 2-fluoro-4-(3-chlorophenoxy)phenyl group, a 2-fluoro-4-(4-chlorophenoxy)phenyl group, a 2-fluoro-4-(2-methylphenoxy)phenyl group, a 2-fluoro-4-(3-methylphenoxy)phenyl group, a 2-fluoro-4-(4-methylphenoxy)phenyl group, a 2-fluoro-4-(2-methoxyphenoxy)phenyl group, a 2-fluoro-4-(3-methoxyphenoxy)phenyl group, a 2-fluoro-4-(4-methoxyphenoxy)phenyl group, a 2-fluoro-4-(2-cyanophenoxy)phenyl group, a 2-fluoro-4-(3-cyanophenoxy)phenyl group, a 2-fluoro-4-(4-cyanophenoxy)phenyl group,
a 4-benzyloxyphenyl group, a 2-fluoro-4-(2-fluorophenylmethoxy)phenyl group, a 2-fluoro-4-(3-fluorophenylmethoxy)phenyl group, a 2-fluoro-4-(4-fluorophenylmethoxy)phenyl group, a 2-fluoro-4-(3,5-difluorophenylmethoxy)phenyl group, a 2-fluoro-4-(2-chlorophenylmethoxy)phenyl group, a 2-fluoro-4-(3-chlorophenylmethoxy)phenyl group, a 2-fluoro-4-(4-chlorophenylmethoxy)phenyl group, a 2-fluoro-4-(2-methylphenylmethoxy)phenyl group, a 2-fluoro-4-(3-methylphenylmethoxy)phenyl group, a 2-fluoro-4-(4-methylphenylmethoxy)phenyl group, a 2-fluoro-4-(2-methoxyphenylmethoxy)phenyl group, a 2-fluoro-4-(3-methoxyphenylmethoxy)phenyl group, a 2-fluoro-4-(4-methoxyphenylmethoxy)phenyl group, a 2-fluoro-4-(2-cyanophenylmethoxy)phenyl group, a 2-fluoro-4-(3-cyanophenylmethoxy)phenyl group, a 2-fluoro-4-(4-cyanophenylmethoxy)phenyl group, a 2-fluoro-4-benzylaminophenyl group, a 2-fluoro-4-(N-benzyl-N-methylamino)phenyl group, a 2-fluoro-4-(2-furylmethoxy)phenyl group, a 2-fluoro-4-(3-furylmethoxy)phenyl group, a 2-fluoro-4-(2-thienylmethoxy)phenyl group, a 2-fluoro-4-(3-thienylmethoxy)phenyl group, a 2-fluoro-4-(2-pyridylmethoxy)phenyl group, a 2-fluoro-4-(3-pyridylmethoxy)phenyl group, a 2-fluoro-4-(4-pyridylmethoxy)phenyl group, a 2-fluoro-4-(2-pyridyloxy)phenyl group, a 2-fluoro-4-(3-pyridyloxy)phenyl group, a 2-fluoro-4-(4-pyridyloxy)phenyl group, a 2-fluoro-4-(6-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-4-(5-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl group, a 2-fluoro-4-(2-pyrazinyloxy)phenyl group, a 2-fluoro-4-(6-chloropyridazin-3-yloxy)phenyl group, a 2-fluoro-4-methoxyphenyl group, a 2-fluoro-4-ethoxyphenyl group, a 2-fluoro-4-propoxyphenyl group, a 2-fluoro-4-(2-methylethoxy)phenyl group, a 2-fluoro-4-butoxyphenyl group, a 2-fluoro-4-(2-methylbutoxy)phenyl group, a 2-fluoro-4-(3-methylbutoxy)phenyl group, a 2-fluoro-4-pentyloxyphenyl group, a 2-fluoro-4-hexyloxyphenyl group, a 2-fluoro-4-heptyloxyphenyl group, a 2-fluoro-4-isoprenyloxyphenyl group, a 2-fluoro-4-(2-fluoroethoxy)phenyl group, a 2-fluoro-4-(3-fluoropropoxy)phenyl group, a 2-fluoro-4-(4-fluorobutoxy)phenyl group, a 2-fluoro-4-(5-fluoropentyloxy)phenyl group, a 2-fluoro-4-(6-fluorohexyloxy)phenyl group, a 2-fluoro-4-(7-fluoroheptyloxy)phenyl group, a 2-fluoro-4-(2-chloroethoxy)phenyl group, a 2-fluoro-4-(3-chloropropoxy)phenyl group, a 2-fluoro-4-(4-chlorobutoxy)phenyl group, a 2-fluoro-4-(5-chloropentyloxy)phenyl group, a 2-fluoro-4-(6-chlorohexyloxy)phenyl group, a 2-fluoro-4-(7-chloroheptyloxy)phenyl group, a 2-fluoro-4-(2-propenyloxy)phenyl group, a 2-fluoro-4-(2-butenyloxy)phenyl group, a 2-fluoro-4-(3-butenyloxy)phenyl group, a 2-fluoro-4-(2-pentenyloxy)phenyl group, a 2-fluoro-4-(3-pentenyloxy)phenyl group, a 2-fluoro-4-(4-pentenyloxy)phenyl group, a 2-fluoro-4-(2-hexenyloxy)phenyl group, a 2-fluoro-4-(3-hexenyloxy)phenyl group, a 2-fluoro-4-(4-hexenyloxy)phenyl group, a 2-fluoro-4-(5-hexenyloxy)phenyl group, a 2-fluoro-4-(2-heptenyloxy)phenyl group, a 2-fluoro-4-(3-heptenyloxy)phenyl group, a 2-fluoro-4-(4-heptenyloxy)phenyl group, a 2-fluoro-4-(5-heptenyloxy)phenyl group, a 2-fluoro-4-(6-heptenyloxy)phenyl group, a 2-fluoro-4-(3-chloro-2-propenyloxy)phenyl group, a 2-fluoro-4-(3,3-dichloro-2-propenyloxy)phenyl group, a 2-fluoro-4-(2-methyl-2-butenyloxy)phenyl group, a 2-fluoro-4-(3-methyl-2-butenyloxy)phenyl group, a 2-fluoro-4-(2-propynyloxy)phenyl group, a 2-fluoro-4-(2-butynyloxy)phenyl group, a 2-fluoro-4-(3-butynyloxy)phenyl group, a 2-fluoro-4-(2-pentynyloxy)phenyl group, a 2-fluoro-4-(3-pentynyloxy)phenyl group, a 2-fluoro-4-(4-pentynyloxy)phenyl group, a 2-fluoro-4-(2-hexynyloxy)phenyl group, a 2-fluoro-4-(3-hexynyloxy)phenyl group, a 2-fluoro-4-(4-hexynyloxy)phenyl group, a 2-fluoro-4-(5-hexynyloxy)phenyl group, a 2-fluoro-4-(2-heptynyloxy)phenyl group, a 2-fluoro-4-(3-heptynyloxy)phenyl group, a 2-fluoro-4-(4-heptynyloxy)phenyl group, a 2-fluoro-4-(5-heptynyloxy)phenyl group, a 2-fluoro-4-(6-heptynyloxy)phenyl group, a 4-(2-methoxyethoxy)phenyl group, a 2-fluoro-4-(3-methoxypropoxy)phenyl group, a 2-fluoro-4-(4-methoxybutoxy)phenyl group, a 2-fluoro-4-(5-methoxypentyloxy)phenyl group, a 2-fluoro-4-(6-methoxyhexyloxy)phenyl group, a 2-fluoro-4-(7-methoxyheptyloxy)phenyl group, a 2-fluoro-4-(2-ethoxyethoxy)phenyl group, a 2-fluoro-4-(3-ethoxypropoxy)phenyl group, a 2-fluoro-4-(4-ethoxybutoxy)phenyl group, a 2-fluoro-4-(5-ethoxypentyloxy)phenyl group, a 2-fluoro-4-(6-ethoxyhexyloxy)phenyl group, a 2-fluoro-4-(7-ethoxyheptyloxy)phenyl group, a 2-fluoro-4-cyclopropylmethoxyphenyl group, a 2-fluoro-4-(2-cyclopropylethoxy)phenyl group, a 2-fluoro-4-(3-cyclopropylpropoxy)phenyl group, a 2-fluoro-4-(4-cyclopropylbutoxy)phenyl group, a 2-fluoro-4-(5-cyclopropylpentyloxy)phenyl group, a 2-fluoro-4-(6-cyclopropylhexyloxy)phenyl group, a 2-fluoro-4-(7-cyclopropylheptyloxy)phenyl group, a 2-fluoro-4-phenoxymethylphenyl group, a 2-fluoro-4-(2-phenylethyl)phenyl group, a 2-fluoro-4-(3-phenylpropyl)phenyl group, a 2-fluoro-4-(4-phenylbutyl)phenyl group, a 2-fluoro-4-(5-phenylpentyl)phenyl group, a 2-fluoro-4-(2-phenylethoxy)phenyl group, a 2-fluoro-4-(3-phenylpropoxy)phenyl group, a 2-fluoro-4-(4-phenylbutoxy)phenyl group, a 2-fluoro-4-(5-phenylpentyloxy)phenyl group, a (Z)-2-fluoro-4-styrylphenyl group, a 1-benzylpyrrol-3-yl group, a 1-(2-fluorophenylmethyl)pyrrol-3-yl group, a 1-(3-fluorophenylmethyl)pyrrol-3-yl group, a 1-(4-fluorophenylmethyl)pyrrol-3-yl group, a 1-(2-phenylethyl)pyrrol-3-yl group, a 1-benzylpyrazol-4-yl group, a 1-phenylpyrazol-4-yl group, a 2-methoxythiazol-5-yl group, a 2-ethoxythiazol-5-yl group, a 2-propoxythiazol-5-yl group, a 2-butoxythiazol-5-yl group, a 2-pentyloxythiazol-5-yl group, a 2-benzyloxythiazol-5-yl group, a 2-phenoxythiazol-5-yl group, a 2-methylthiazol-5-yl group, a 2-butylthiazol-5-yl group, a 2-phenylthiazol-5-yl group and a 2-benzylthiazol-5-yl group.
A preferred example of the present compound may be a compound wherein Z represents an oxygen atom; E represents a 2-furyl group that may optionally have one substituent selected from the substituent group g-1 and the substituent group g-2, a 2-thienyl group that may optionally have one substituent selected from the substituent group g-1 and the substituent group g-2, a 3-pyrrolyl group that may optionally have one substituent selected from the substituent group g-1 and the substituent group g-2, or a phenyl group that may optionally have one substituent selected from the substituent group g-1 and the substituent group g-2; R1 represents a hydrogen atom; R2 represents a hydrogen atom or a halogen atom; and R3 represents a group selected from the substituent group c-21 and the substituent group c-22.
Examples of the present compound include the following compounds.
An amide compound represented by formula (2):
wherein R4 represents a halogen atom, a C1-C3 alkyl group, an ethynyl group, a C1-C4 alkoxy group, a methylthio group, a trifluoromethyl group or a trifluoromethoxy group, n represents 1 or 2 wherein in the case of n being 2, R in each occurrence is the same or different from each other;
an amide compound of the formula (2) wherein n is 1;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 3-position or the 4-position;
an amide compound of the formula (2) wherein R4 is a fluorine atom, a trifluoromethyl group or a trifluoromethoxy group bound to the 3-position or the 4-position;
an amide compound of the formula (2) wherein R4n is one or two halogen atoms;
an amide compound of the formula (2) wherein R4n is one or two C1-C3 alkyl groups;
an amide compound of the formula (2) wherein R4n is one or two ethynyl groups;
an amide compound of the formula (2) wherein R4n is one or two C1-C4 alkoxy groups;
an amide compound of the formula (2) wherein R4n is one or two methylthio groups;
an amide compound of the formula (2) wherein R4n is one or two trifluoromethyl groups;
an amide compound of the formula (2) wherein R4n is one or two trifluoromethoxy groups;
an amide compound of the formula (2) wherein n is 1;
an amide compound of the formula (2) wherein n is 2;
an amide compound of the formula (2) wherein n is 1 and the binding position of R4 is the 3-position;
an amide compound of the formula (2) wherein n is 1 and the binding position of R4 is the 4-position;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 3-position, and R is a halogen atom;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 3-position, and R is a C1-C3 alkyl group;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 3-position, and R is a C1-C4 alkoxy group;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 4-position, and R is a halogen atom;
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 4-position, and R is a C1-C3 alkyl group, and
an amide compound of the formula (2) wherein n is 1, the binding position of R4 is the 4-position and R is a C1-C4 alkoxy group.
An amide compound represented by formula (3)
wherein R5 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group;
an amide compound of formula (3) wherein the binding potion of R5 is the 3-position or the 4-position;
an amide compound of formula (3) wherein R5 is a fluorine atom bound to the 3-position, a fluorine atom bound to the 4-position, a trifluoromethyl group bound to the 3-position, a trifluoromethyl group bound to the 4-position, a trifluoromethoxy group bound to the 3-position or a trifluoromethoxy group bound to the 4-position;
an amide compound of formula (3) wherein R5 is a hydrogen atom;
an amide compound of formula (3) wherein R5 is a halogen atom;
an amide compound of formula (3) wherein R5 is a methyl group;
an amide compound of formula (3) wherein R5 is a methoxy group;
an amide compound of formula (3) wherein R5 is a trifluoromethyl group;
an amide compound of formula (3) wherein R5 is a trifluoromethoxy group;
an amide compound of formula (3) wherein the binding position of R5 is the 2-position;
an amide compound of formula (3) wherein the binding position of R5 is the 3-position;
an amide compound of formula (3) wherein the binding position of R5 is the 4-position;
an amide compound of formula (3) wherein the binding position of R5 is the 2-position and R5 is a halogen atom;
an amide compound of formula (3) wherein the binding position of R5 is the 3-position and R5 is a halogen atom, and
an amide compound of formula (3) wherein the binding position of R5 is the 4-position and R5 is a halogen atom.
An amide compound represented by formula (4)
wherein R6 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group;
an amide compound of the formula (4) wherein the binding position of R6 is the 3-position or the 4-position;
an amide compound of the formula (4) wherein R6 is a fluorine atom bound to the 3-position, a fluorine atom bound to the 4-position, a trifluoromethyl group bound to the 3-position; a trifluoromethyl group bound to the 4-position, a trifluoromethoxy group bound to the 3-position or a trifluoromethoxy group bound to the 4-position;
an amide compound of the formula (4) wherein R6 is a halogen atom;
an amide compound of the formula (4) wherein R6 is a methyl group;
an amide compound of the formula (4) wherein R6 is a methoxy group;
an amide compound of the formula (4) wherein R6 is a trifluoromethyl group;
an amide compound of the formula (4) wherein R6 is a trifluoromethoxy group;
an amide compound of the formula (4) wherein the binding position of R6 is the 2-position;
an amide compound of the formula (4) wherein the binding position of R6 is the 3-position;
an amide compound of the formula (4) wherein the binding position of R6 is the 4-position;
an amide compound of the formula (4) wherein the binding position of R6 is the 2-position and R6 is a halogen atom;
an amide compound of the formula (4) wherein the binding position of R6 is the 3-position and R6 is a halogen atom; and
an amide compound of the formula (4) wherein the binding position of R6 is the 4-position and R6 is a halogen atom.
An amide compound represented by formula (5)
wherein R7 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position or the 4-position;
an amide compound of the formula (5) wherein R7 is a fluorine atom bound to the 3-position, a fluorine atom bound to the 4-position, a trifluoromethyl group bound to the 3-position, a trifluoromethyl group bound to the 4-position, a trifluoromethoxy group bound to the 3-position or a trifluoromethoxy group bound to the 4-position;
an amide compound of the formula (5) wherein R7 is a hydrogen atom;
an amide compound of the formula (5) wherein R7 is a halogen atom;
an amide compound of the formula (5) wherein R7 is a methyl group;
an amide compound of the formula (5) wherein R7 is a methoxy group;
an amide compound of the formula (5) wherein R7 is a trifluoromethyl group;
an amide compound of the formula (5) wherein R7 is a trifluoromethoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position;
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position and R7 is a halogen atom;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position and R7 is a halogen atom;
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position and R7 is a halogen atom;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position and R7 is a methyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position and R7 is a methyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position and R7 is a methyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position and R7 is a methoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position and R7 is a methoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position and R7 is a methoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position and R7 is a trifluoromethyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position and R7 is a trifluoromethyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position and R7 is a trifluoromethyl group;
an amide compound of the formula (5) wherein the binding position of R7 is the 2-position and R7 is a trifluoromethoxy group;
an amide compound of the formula (5) wherein the binding position of R7 is the 3-position and R7 is a trifluoromethoxy group; and
an amide compound of the formula (5) wherein the binding position of R7 is the 4-position and R7 is a trifluoromethoxy group.
An amide compound represented by formula (6)
wherein R8 represents a hydrogen atom, a fluorine atom, a methyl group or a methoxymethyl group, R9 represents a hydrogen atom, a halogen atom, a C1-5 alkyl group, a C1-4 linear alkoxy group, a C1-2 alkylthio group, a trifluoromethyl group, a trifluoromethoxy group or a cyano group, m represents 1, 2 or 3, wherein when m is 2 or 3, R9's are the same or different from each other;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position or the 4-position;
an amide compound of the formula (6) wherein m is 1 and R9 is a fluorine atom bound to the 3-position, a fluorine atom bound to the 4-position, a trifluoromethyl group bound to the 3-position, a trifluoromethyl group bound to the 4-position, a trifluoromethoxy group bound to the 3-position or a trifluoromethoxy group bound to the 4-position;
an amide compound of the formula (6) wherein R8 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom;
an amide compound of the formula (6) wherein R8 is a methyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group;
an amide compound of the formula (6) wherein R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R9 is one, two or three halogen atoms;
an amide compound of the formula (6) wherein R9 is one, two or three C1-5 alkyl groups;
an amide compound of the formula (6) wherein R9 is one, two or three C1-4 linear alkoxy groups;
an amide compound of the formula (6) wherein R9 is one, two or three C1-2 alkylthio groups;
an amide compound of the formula (6) wherein R9 is one, two or three trifluoromethyl groups;
an amide compound of the formula (6) wherein R9 is one, two or three trifluoromethoxy groups;
an amide compound of the formula (6) wherein R9 is one, two or three cyano groups;
an amide compound of the formula (6) wherein m is 1;
an amide compound of the formula (6) wherein m is 2;
an amide compound of the formula (6) wherein m is 3;
an amide compound of the formula (6) wherein m is 1 and the binding position of R9 is the 2-position;
an amide compound of the formula (6) wherein m is 1 and the binding position of R9 is the 3-position;
an amide compound of the formula (6) wherein m is 1 and the binding position of R9 is the 4-position;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and the binding position of R9 is the 2-position;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and the binding position of R9 is the 3-position;
an amide compound of the formula (6) wherein R8 is a hydrogen atom , m is 1 and the binding position of R9 is the 4-position;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and the binding position of R9 is the 2-position;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and the binding position of R9 is the 3-position;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and the binding position of R9 is the 4-position;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and the binding position of R9 is the 2-position;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and the binding position of R9 is the 3-position;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and the binding position of R9 is the 4-position;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and the binding position of R9 is the 2-position;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and the binding position of R9 is the 3-position;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and the binding position of R9 is the 4-position;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1 and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein m is 1, the binding position of R9 is the 4-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a fluorine atom and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methyl group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methoxymethyl group, m is 1, the binding position of R9 is the 2-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a fluorine atom and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methyl group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 3-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a hydrogen atom, m is 1, the binding position of R9 is the 4-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a fluorine atom and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9R7 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a fluorine atom, m is 1, the binding position of R9 is the 4-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methyl group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group;
an amide compound of the formula (6) wherein R8 is a methyl group, m is 1, the binding position of R9 is the 4-position and R9 is a cyano group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group and R9 is a hydrogen atom;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a halogen atom;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-5 alkyl group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-4 linear alkoxy group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a C1-2 alkylthio group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethyl group;
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a trifluoromethoxy group; and
an amide compound of the formula (6) wherein R8 is a methylmethoxy group, m is 1, the binding position of R9 is the 4-position and R9 is a cyano group.
An amide compound represented by formula (7)
wherein R10 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group, R11 represents a C1-C7 linear alkyl group, a C3-C7 linear alkenyl group or a C3-C7 linear alkynyl group;
an amide compound of the formula (7) wherein R11 is a methyl group, a pentyl group, a pentenyl group or a pentynyl group;
an amide compound of the formula (7) wherein R10 is a hydrogen atom;
an amide compound of the formula (7) wherein R10 is a fluorine atom;
an amide compound of the formula (7) wherein R10 is a methyl group;
an amide compound of the formula (7) wherein R10 is a methoxymethyl group;
an amide compound of the formula (7) wherein R11 is a C1-C7 linear alkyl group;
an amide compound of the formula (7) wherein R11 is a C3-C7 linear alkenyl group;
an amide compound of the formula (7) wherein R11 is a C3-C7 linear alkynyl group;
an amide compound of the formula (7) wherein R10 is a hydrogen atom and R11 is a C1-C7 linear alkyl group;
an amide compound of the formula (7) wherein R10 is a hydrogen atom and R11 is a C3-C7 linear alkenyl group;
an amide compound of the formula (7) wherein R10 is a hydrogen atom and R11 is a C3-C7 linear alkynyl group;
an amide compound of the formula (7) wherein R10 is a fluorine atom and R11 is a C1-C7 linear alkyl group;
an amide compound of the formula (7) wherein R10 is a fluorine atom and R11 is a C3-C7 linear alkenyl group;
an amide compound of the formula (7) wherein R10 is a fluorine atom and R11 is a C3-C7 linear alkynyl group;
an amide compound of the formula (7) wherein R10 is a methyl group and R11 is a C1-C7 linear alkyl group;
an amide compound of the formula (7) wherein R10 is a methyl group and R11 is a C3-C7 linear alkenyl group;
an amide compound of the formula (7) wherein R10 is a methyl group and R11 is a C3-C7 linear alkynyl group;
an amide compound of the formula (7) wherein R10 is a methoxymethyl group and R11 is a C1-C7 linear alkyl group;
an amide compound of the formula (7) wherein R10 is a methoxymethyl group and R11 is a C3-C7 linear alkenyl group, and
an amide compound of the formula (7) wherein R10 is a methoxymethyl group and R11 is a C3-C7 linear alkynyl group.
An amide compound represented by formula (8)
wherein R12 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group, R13 represents a C5-C7 linear alkyl group, a C5-C7 linear alkenyl group or a C5-C7 linear alkynyl group;
an amide compound of the formula (8) wherein R13 is a pentyl group, a pentenyl group or a pentynyl group;
an amide compound of the formula (8) wherein R12 is a hydrogen atom ;
an amide compound of the formula (8) wherein R12 is a fluorine atom;
an amide compound of the formula (8) wherein R12 is a methyl group;
an amide compound of the formula (8) wherein R12 is a methoxymethyl group;
an amide compound of the formula (8) wherein R13 is a C5-C7 linear alkyl group;
an amide compound of the formula (8) wherein R13 is a C5-C7 linear alkenyl group;
an amide compound of the formula (8) wherein R13 is a C5-C7 linear alkynyl group;
an amide compound of the formula (8) wherein R12 is a hydrogen atom and R13 is a C5-C7 linear alkyl group;
an amide compound of the formula (8) wherein R12 is a hydrogen atom and R13 is a C5-C7 linear alkenyl group;
an amide compound of the formula (8) wherein R12 is a hydrogen atom and R13 is a C5-C7 linear alkynyl group;
an amide compound of the formula (8) wherein R12 is a fluorine atom and R13 is a C5-C7 linear alkyl group;
an amide compound of the formula (8) wherein R12 is a fluorine atom and R13 is a C5-C7 linear alkenyl group;
an amide compound of the formula (8) wherein R12 is a fluorine atom and R13 is a C5-C7 linear alkynyl group;
an amide compound of the formula (8) wherein R12 is a methyl group and R13 is a C5-C7 linear alkyl group;
an amide compound of the formula (8) wherein R12 is a methyl group and R13 is a C5-C7 linear alkenyl group;
an amide compound of the formula (8) wherein R12 is a methyl group and R13 is a C5-C7 linear alkynyl group;
an amide compound of the formula (8) wherein R12 is a methoxymethyl group and R13 is a C5-C7 linear alkyl group;
an amide compound of the formula (8) wherein R12 is a methoxymethyl group and R13 is a C5-C7 linear alkenyl group and
an amide compound of the formula (8) wherein R12 is a methoxymethyl group and R13 is a C5-C7 linear alkynyl group.
An amide compound represented by formula (9)
wherein R14 represents a hydrogen atom, a halogen atom, a methyl group, a methoxy group, a trifluoromethyl group or a trifluoromethoxy group, R15 represents a C3-7 linear alkyl group;
an amide compound of the formula (9) wherein R14 is a hydrogen atom, R15 is a pentyl group or a hexyl group;
an amide compound of the formula (9) wherein R14 is a hydrogen atom;
an amide compound of the formula (9) wherein R14 is a fluorine atom;
an amide compound of the formula (9) wherein R14 is a methyl group;
an amide compound of the formula (9) wherein R14 is a methoxymethyl group;
an amide compound of the formula (9) wherein R15 is a propyl group;
an amide compound of the formula (9) wherein R15 is a butyl group;
an amide compound of the formula (9) wherein R15 is a pentyl group;
an amide compound of the formula (9) wherein R15 is a hexyl group and
an amide compound of the formula (9) wherein R15 is a heptyl group.
The following compounds 1 to 248 as shown in Tables 1 to 10 are specific examples of the present compound. These compounds are shown as combinations of R1, R2, R3, Z and E in the following formula (2).
As the present compound, the following compounds are specifically mentioned.
N-(3-phenyloxyphenyl)methyl-2-amino-6-methoxymethylnicotinic acid amide,
N-(3-phenyloxyphenyl)methyl-2-amino-6-fluoronicotinic acid amide,
N-[3-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide,
N-(4-phenyloxyphenyl)methyl-2-aminonicotinic acid amide,
N-(2-fluoro-3-methoxyphenyl)methyl-2-aminonicotinic acid amide,
N-(3-pentyloxyphenyl)methyl-2-aminonicotinic acid amide,
N-(4-propylphenyl)methyl-2-aminonicotinic acid amide,
In the present specification, as a matter of convenience, the structural formulae of compounds may indicate certain isomers. However, the present invention includes all active isomers such as geometric isomers, optical isomers, steric isomers and tautomers and isomeric mixtures, which are generated due to the structures of compounds. Thus, the present invention is not limited to the descriptions of such convenient formulae. The present invention may include either such an isomer or such a mixture. Accordingly, the compound of the present invention may have an asymmetric carbon atom in a molecule thereof, and optically active compounds and racemic compounds may be present. However, in the present invention, such optically active compounds or racemic compounds is not particularly limited, and all these cases are included in the present invention.
The present compound can be produced by the production method described in International Patent Application No. WO2005/033079, or by the after-mentioned (production method 1) to (production method 5).
Among the present compounds, compound (4) wherein Z represents an oxygen atom can be produced by allowing compound (2) or a salt thereof (a hydrochloride, for example) to react with compound (3) in the presence of a dehydrating condensing reagent,
wherein R1, R2, R3 and E have the same meanings as defined above.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as tetrahydrofuran (hereinafter referred to as THF, at times), ethylene glycol dimethyl ether, or tert-butyl methyl ether (hereinafter referred to as MTBE, at times); aliphatic hydrocarbons such as hexane, heptane, or octane; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; esters such as butyl acetate or ethyl acetate; nitriles such as acetonitrile; acid amides such as N,N-dimethylformamide (hereinafter referred to as DMF, at times); sulfoxides such as dimethyl sulfoxide (hereinafter referred to as DMSO, at times); and the mixtures thereof.
Examples of a dehydrating condensing reagent used in the reaction include: carbodiimides such as 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (hereinafter referred to as WSC) and 1,3-dicyclohexylcarbodiimide; and phosphonium salts such as (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (hereinafter referred to as a “BOP reagent”).
Compound (3) is generally used in an amount of 1 to 3 moles with respect to 1 mole of compound (2). Such a dehydrating condensing reagent is generally used in an amount of 1 to 5 moles with respect to 1 mole of compound (2).
The reaction temperature applied to the reaction is generally between 0° C. and 140° C. The reaction time is generally between 1 and 24 hours.
After completion of the reaction, the reaction mixture is filtrated, and the filtrate is then extracted with an organic solvent. The organic layer is dried and is then concentrated, so as to isolate compound (4). The isolated compound (4) may be subjected to chromatography, recrystallization, etc., so that it can be further purified.
Among the present compounds, compound (6) wherein Z represents a sulfur atom can be produced by allowing the compound (4) wherein Z represents an oxygen atom to react with 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetan-2,4-disulfide (hereinafter referred to as a “Lawesson's reagent”) or a sulfurizing reagent such as phosphorus pentasulfide,
wherein R1, R2, R3 and E have the same meanings as defined above.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as THF, ethylene glycol dimethyl ether, or MTBE; aliphatic hydrocarbons such as hexane, heptane, or octane; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; organic nitriles such as acetonitrile or butyronitrile; sulfoxides such as dimethyl sulfoxide; and the mixtures thereof.
The Lawesson's reagent is generally used in an amount of 1 to 2 moles with respect to 1 mole of compound (4).
The reaction temperature applied to the reaction is generally between 25° C. and 150° C. The reaction time is generally between 0.1 and 24 hours.
After completion of the reaction, the reaction mixture is extracted with an organic solvent. Thereafter, the organic layer is dried, and it is then concentrated, so as to isolate compound (6). The isolated compound (6) may be subjected to chromatography, recrystallization, etc., so that it can be further purified.
Among the present compounds, compound (9) can be produced by allowing compound (7) to react with compound (8) in the presence of a base,
wherein R1, R2 and R3 have the same meanings as defined above; E1 represents a furyl group, a thienyl group, a pyrrolyl group, a tetrazolyl group, a thiazolyl group, a pyrazolyl group, or a phenyl group wherein E1 may have one substituent selected from the aforementioned substituent group a-1 and substituent group a-2; L represents a chlorine atom, a bromine atom, an iodine atom, a methanesulfonyloxy group, a trifluoromethanesulfonyloxy group or a p-toluenesulfonyloxy group; R2-1 represents a substituent selected from the following substituent group e-1 and substituent group e-2:
[Substituent Group e-1]
C1-8 alkyl group, C3-9 alkenyl group, C3-9 alkynyl group, C3-8 cycloalkyl group, C6-10 aryl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, and 5- to 10-membered heterocylic C1-6 alkyl group; and
[Substituent Group e-2]
C1-8 alkyl group, C3-9 alkenyl group, C3-9 alkynyl group, C3-8 cycloalkyl group, 5- to 10-membered heterocyclic group, C3-8 cycloalkyl C1-6 alkyl group, C6-10 aryl C1-6 alkyl group, and 5- to 10-membered heterocylic C1-6 alkyl group;
wherein each group described in the substituent group e-2 has one to three substituents selected from the following substituent group f:
halogen atom, cyano group, C1-6 alkyl group, C1-6 alkoxy group, and trifluoromethyl group.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as THF, ethylene glycol dimethyl ether, or MTBE; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; nitriles such as acetonitrile; acid amides such as DMF; sulfoxides such as dimethyl sulfoxide; ketones such as acetone, methyl ethyl ketone, or methyl isobutyl ketone; water; and the mixtures thereof.
Examples of a base used in the reaction include: alkali metal carbonates such as sodium carbonate, potassium carbonate, or cesium carbonate; alkali metal hydroxides such as sodium hydroxide; and alkali metal hydrides such as sodium hydride.
Compound (8) is generally used in an amount of 1 to 10 moles with respect to 1 mole of compound (7), and a base is generally used in an amount of 1 to 5 moles with respect to 1 mole of compound (7).
The reaction temperature applied to the reaction is generally between −20° C. and 100° C. The reaction time is generally between 0.1 and 24 hours.
After completion of the reaction, water is added to the reaction mixture. When a solid is precipitated, it is filtrated to isolate compound (9). When such a solid is not precipitated, the reaction mixture is extracted with an organic solvent, and the organic layer is then dried and concentrated, so as to isolate compound (9). The isolated compound (9) may be subjected to chromatography, recrystallization, etc., so that the organic layer can be further purified.
The compound (4) can also be produced by the following scheme:
wherein R1, R2, R3 and E have the same meanings as defined above.
Compound (11) can be produced by allowing compound (2) or a salt thereof (a hydrochloride, for example) to react with compound (10) according to the method described in production method 1.
Compound (4) can be produced by allowing compound (11) to react with ammonia.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as THF, ethylene glycol dimethyl ether, or MTBE; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; nitriles such as acetonitrile; acid amides such as DMF; sulfoxides such as dimethyl sulfoxide; alcohols such as methanol, ethanol, or 1,1-dimethylethanol; water; and the mixtures thereof.
Ammonia is generally used in an amount ranging from 1 mole to an excessive amount with respect to 1 mole of compound (11).
The reaction temperature applied to the reaction is generally between −10° C. and 250° C. The reaction time is generally between 0.1 and 24 hours.
After completion of the reaction, water is added to the reaction mixture. When a solid is precipitated, it is filtrated to isolate compound (4). When such a solid is not precipitated, the reaction mixture is extracted with an organic solvent, and the organic layer is then dried and concentrated, so as to isolate compound (4). The isolated compound (4) may be subjected to chromatography, recrystallization, etc., so that the organic layer can be further purified.
The compound (4) can also be produced by the following scheme:
wherein R1, R2, R3 and E have the same meanings as defined above.
Compound (12) can be produced by allowing compound (11) to react with an azide compound.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as THF, ethylene glycol dimethyl ether, or MTBE; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; nitriles such as acetonitrile; acid amides such as DMF; sulfoxides such as dimethyl sulfoxide; water; and the mixtures thereof.
As an azide compound, sodium azide, trimethylsilylazide, etc. can be used.
Such an azide compound is generally used in an amount of 1 mole to in an excessive amount with respect to 1 mole of compound (11).
The reaction temperature applied to the reaction is generally between 50° C. and 150° C. The reaction time is generally between 0.1 and 24 hours.
After completion of the reaction, water is added to the reaction mixture. When a solid is precipitated, it is filtrated to isolate compound (12). When such a solid is not precipitated, the reaction mixture is extracted with an organic solvent, and the organic layer is then dried and concentrated, so as to isolate compound (12). The isolated compound (12) may be subjected to chromatography, recrystallization, etc., so that it can be further purified.
The compound (4) can be produced by allowing the compound (12) to react with a reducing reagent.
This reaction is generally carried out in the presence of a solvent.
Examples of a solvent used in the reaction include: ethers such as THF, ethylene glycol dimethyl ether, or MTBE; aromatic hydrocarbons such as toluene or xylene; halogenated hydrocarbons such as chlorobenzene; nitriles such as acetonitrile; acid amides such as DMF; sulfoxides such as dimethyl sulfoxide; water; and the mixtures thereof.
A reducing reagent is generally used in an amount ranging from 1 mole to an excessive amount with respect to 1 mole of compound (12).
Examples of such a reducing reagent include tin chloride, hydrogen+palladium catalyst, and triphenylphosphine+water.
The reaction temperature applied to the reaction is generally between −20° C. and 150° C. The reaction time is generally between 0.1 and 24 hours.
After completion of the reaction, water is added to the reaction mixture. When a solid is precipitated, it is filtrated to isolate compound (4). When such a solid is not precipitated, the reaction mixture is extracted with an organic solvent, and the organic layer is then dried and concentrated, so as to isolate compound (4). The isolated compound (4) may be subjected to chromatography, recrystallization, etc., so that it can be further purified.
In the case of the agricultural composition of the present invention, in general, the present compound is mixed with a liquid carrier, a solid carrier, a gas carrier, a surfactant, etc. Thereafter, formulation auxiliary reagents such as a binder or a thickener are added thereto, as necessary, so that the mixture can be formulated into a wettable powder, a granulated wettable powder, a flowable reagent, a granule, a dry flowable reagent, an emulsion, an aqueous liquid reagent, an oil reagent, a smoking reagent, an aerosol, a microcapsule, etc., and the thus produced formulations can be then used. The present compound is comprised in such a formulation at a weight ratio generally between 0.1% and 99%, and preferably between 0.2% and 90%.
Examples of a liquid carrier used in formulation include water, alcohols (e.g. methanol, ethanol, 1-propanol, 2-propanol, ethylene glycol, etc.), ketones (e.g. acetone, methyl ethyl ketone, etc.), ethers (e.g. dioxane, tetrahydrofuran, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, propylene glycol monomethyl ether, etc.), aliphatic hydrocarbons (e.g. hexane, octane, cyclohexane, coal oil, fuel oil, machine oil, etc.), aromatic hydrocarbons (e.g. benzene, toluene, xylene, solvent naphtha, methylnaphthalene, etc.), halogenated hydrocarbons (e.g. dichloromethane, chloroform, carbon tetrachloride, etc.), acid amides (e.g. dimethylformamide, dimethylacetamide, N-methylpyrrolidone, etc.), esters (e.g. ethyl acetate, butyl acetate, fatty acid glycerin ester, etc.), and nitriles (e.g. acetonitrile, propionitrile, etc.). Two or more types of such liquid carriers can be mixed at an appropriate ratio and can be then used.
Examples of a solid carrier used in formulation include vegetable powders (e.g. soybean powder, tobacco powder, wheat flour, wood flour, etc.), mineral powders (e.g. clays such as kaoline, bentonite, acid clay, or clay; talcs such as talcum powder or pyrophyllite powder; silicas such as diatomaceous earth or mica powder; etc.), alumina, sulfur powder, activated carbon, sugars (e.g. lactose, glucose, etc.), inorganic salts (e.g. calcium carbonate, sodium bicarbonate, etc.), and a glass hollow body (produced by subjecting a natural holohyaline to a burning process and then encapsulating air bubbles therein). Two or more types of such solid carriers can be mixed at an appropriate ratio and can be then used. Such liquid carrier or solid carrier is used at a ratio generally between 1% to 99% by weight, and preferably between approximately 10% and 99% by weight, based on the total weight of a pharmaceutical.
As an emulsifier, a dispersant, a spreader, a penetrant, a moisturizer, or the like used in the formulation, a surfactant is generally used. Examples of such a surfactant include: anionic surfactants such as alkyl sulfate ester salts, alkylaryl sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkyl aryl ether phosphates, lignosulfonates, or naphthalenesulfonate formamide polycondensates; and nonionic surfactants such as a polyoxyethylene alkyl ether, a polyoxyethylene alkyl aryl ether, a polyoxyethylene alkyl polyoxy propylene block copolymer, or a sorbitan fatty acid ester. These surfactants can also be used in combination of two or more types. Such a surfactant is used at a ratio generally between 0.1% and 50% by weight, and preferably between approximately 0.1% and 25% by weight, based on the total weight of a pharmaceutical.
Examples of a binder or a thickener include dextrin, sodium salts of carboxymethyl cellulose, a polycarboxylic acid polymer, polyvinylpyrrolidone, polyvinyl alcohol, sodium lignosulfonate, calcium lignosulfonate, sodium polyacrylate, gum Arabic, sodium alginate, mannitol, sorbitol, bentonite mineral matter, polyacrylic acid and a derivative thereof, sodium salts of carboxymethyl cellulose, white carbon, and natural sugar derivatives (e.g. xanthan gum, Cyamoposis Gum, etc.).
Moreover, the agricultural composition of the present invention can be mixed with other types of disinfectants, insecticides, acaricides, nematicides, herbicides, plant growth regulators, fertilizers, or soil improvers, and they can be used. Otherwise, the present agricultural composition can be used together with the aforementioned reagents, without mixing with them.
Examples of such other disinfectants include: azole disinfectant compounds such as propiconazole, prothioconazole, triadimenol, prochloraz, penconazole, tebuconazole, flusilazole, diniconazole, bromuconazole, epoxiconazole, difenoconazole, cyproconazole, metconazole, triflumizole, tetraconazole, microbutanil, fenbuconazole, hexaconazole, fluquinconazole, triticonazole, bitertanol, imazalil, flutriafol, simeconazole, or ipconazole; cyclic amine disinfectant compounds such as fenpropimorph, tridemorph, or fenpropidin; benzimidazole disinfectant compounds such as carbendazim, benomyl, thiabendazole, or thiophanate-methyl; procymidone; cyprodinil; pyrimethanil; diethofencarb; thiuram; fluazinam, mancozeb; iprodione; vinclozolin, chlorothalonil; captan; mepanipyrim, fenpiclonil; fludioxonil; dichlofluanid; folpet; kresoxim-methyl; azoxystrobin; trifloxystrobin; fluoxastrobin; picoxystrobin; pyraclostrobin; dimoxystrobin; pyribencarb; metominostrobin; enestroburin; spiroxamine; quinoxyfen; fenhexamid; famoxadone; fenamidone; zoxamide; etaboxam; amisulbrom; iprovalicarb; benthiavalicarb; cyazofamid; mandipropamid; boscalid; penthiopyrad; metrafenone; fluopyran; bixafen; cyflufenamid; proquinazid; orysastrobin; furametpyr; thifluzamide; mepronil; flutolanil; flusulfamide; fluopicolide; metalaxyl M; kiralaxyl; fosetyl; cymoxanil; pencycuron; tolclofos methyl; carpropamid; diclocymet; fenoxanil; tricyclazole; pyroquilon; probenazole; isotianil; tiadinil; tebufroquin; diclomezine; kasugamycin; ferimzone; fthalide; validamycin; hydroxyisoxazole; iminoctadin-acetate; isoprothiolane; oxolinic acid; oxytetracycline; streptomycin; basic copper chloride; cupric hydroxide; basic copper sulfate; organic copper; and sulfur.
Examples of other insecticides include the following compounds:
acephate, Aluminium phosphide, butathiofos, cadusafos, chlorethoxyfos, chlorfenvinphos, chlorpyrifos, chlorpyrifos-methyl, cyanophos: CYAP, diazinon, DCIP(dichlorodiisopropyl ether), dichlofenthion: ECP, dichlorvos: DDVP, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, etrimfos, fenthion: MPP, fenitrothion: MEP, fosthiazate, formothion, Hydrogen phosphide, isofenphos, isoxathion, malathion, mesulfenfos, methidathion: DMTP, monocrotophos, naled: BRP, oxydeprofos: ESP, parathion, phosalone, phosmet: PMP, pirimiphos-methyl, pyridafenthion, quinalphos, phenthoate: PAP, profenofos, propaphos, prothiofos, pyraclorfos, salithion, sulprofos, tebupirimfos, temephos, tetrachlorvinphos, terbufos, thiometon, trichlorphon: DEP, vamidothion, phorate, cadusafos, etc.;
alanycarb, bendiocarb, benfuracarb, BPMC, carbaryl, carbofuran, carbosulfan, cloethocarb, ethiofencarb, fenobucarb, fenothiocarb, fenoxycarb, furathiocarb, isoprocarb: MIPC, metolcarb, methomyl, methiocarb, NAC, oxamyl, pirimicarb, propoxur: PHC, XMC, thiodicarb, xylylcarb, aldicarb, etc.;
acrinathrin, allethrin, benfluthrin, beta-cyfluthrin, bifenthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin, deltamethrin, esfenvalerate, ethofenprox, fenpropathrin, fenvalerate, flucythrinate, flufenoprox, flumethrin, fluvalinate, halfenprox, imiprothrin, permethrin, prallethrin, pyrethrins, resmethrin, sigma-cypermethrin, silafluofen, tefluthrin, tralomethrin, transfluthrin, tetramethrin, phenothrin, cyphenothrin, alpha-cypermethrin, zeta-cypermethrin, lambda-cyhalothrin, furamethrin, tau-fluvalinate, 2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl(EZ)-(1RS, 3RS; IRS, 3 SR)-2,2-dimethyl-3-prop-1-enyl cyclopropane carboxylate, 2,3,5,6-tetrafluoro-4-methylbenzyl(EZ)-(1RS, 3RS; 1RS, 3SR)-2,2-dimethyl-3-prop-1-enyl cyclopropane carboxylate, 2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl(1RS, 3RS; 1RS, 3SR)-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropane carboxylate, etc.;
cartap, bensultap, thiocyclam, monosultap, bisultap, etc.;
imidacloprid, nitenpyram, acetamiprid, thiamethoxam, thiacloprid, dinotefuran, clothianidin, etc.,
chlorfluazuron, bistrifluoron, diafenthiuron, diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron, triazlon, etc.;
acetoprole, ethiprole, fipronil, vaniliprole, pyriprole, pyrafluprole, etc.;
Fresh spores derived from Bacillus thuringiensis, crystalline toxins generated therefrom, and the mixtures thereof;
chromafenozide, halofenozide, methoxyfenozide, tebufenozide, etc.;
aldrin, dieldrin, dienochlor, endosulfan, methoxychlor, etc.;
machine oil and nicotine-sulfate; and
avermectin-B, bromopropylate, buprofezin, chlorphenapyr, cyromazine, D-D(1,3-Dichloropropene), emamectin-benzoate, fenazaquin, flupyrazofos, hydroprene, methoprene, indoxacarb, metoxadiazone, milbemycin-A, pymetrozine, pyridalyl, pyriproxyfen, spinosad, sulfluramid, tolfenpyrad, triazamate, flubendiamide, lepimectin, Arsenic acid, benclothiaz, Calcium cyanamide, Calcium polysulfide, chlordane, DDT, DSP, flufenerim, flonicamid, flurimfen, formetanate, metam-ammonium, metam-sodium, Methyl bromide, nidinotefuran, Potassium oleate, protrifenbute, spiromesifen, Sulfur, metaflumizone, spirotetramat, pyrifluquinazone, spinetoram, and chlorantraniliprole.
Examples of other types of acaricides (acarcidal active ingredients) include acequinocyl, amitraz, benzoximate, bifenaate, bromopropylate, chinomethionat, chlorobenzilate, CPCBS (chlorfenson), clofentezine, cyflumetofen, kelthane (dicofol), etoxazole, fenbutatin oxide, fenothiocarb, fenpyroximate, fluacrypyrim, fluproxyfen, hexythiazox, propargite: BPPS, polynactins, pyridaben, Pyrimidifen, tebufenpyrad, tetradifon, spirodiclofen, spiromesifen, spirotetramat, amidoflumet, and cyenopyrafen.
Examples of such other types of nematicides (nematicidal active ingredients) include DCIP, fosthiazate, levamisol hydrochloride, methylisothiocyanate; moraltel tartarate, and imicyafos.
The weight ratio between the agricultural composition of the present invention and a disinfectant mixed with or used together with the aforementioned agricultural composition is generally between 1:0.01 and 1:100, and preferably between 1:0.1 and 1:10, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and an insecticide mixed with or used together with the aforementioned agricultural composition is generally between 1:0.01 and 1:100, and preferably between 1:0.1 and 1:10, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and an acaricide mixed with or used together with the aforementioned agricultural composition is generally between 1:0.01 and 1:100, and preferably between 1:0.1 and 1:10, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and a nematicide mixed with or used together with the aforementioned agricultural composition is generally between 1:0.01 and 1:100, and preferably between 1:0.1 and 1:10, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and a herbicide mixed with or used together with the aforementioned agricultural composition is generally between 1:0.01 and 1:100, and preferably between 1:0.1 and 1:10, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and a plant growth regulator mixed with or used together with the aforementioned agricultural composition is generally between 1:0.00001 and 1:100, and preferably between 1:0.0001 and 1:1, in terms of active ingredient.
The weight ratio between the agricultural composition of the present invention and a fertilizer or soil improver mixed with or used together with the aforementioned agricultural composition is generally between 1:0.1 and 1:1000, and preferably between 1:1 and 1:200.
The type of a method of applying the agricultural composition of the present invention is not particularly limited, as long as the agricultural composition of the present invention can be substantially applied by the method. Examples of such an application method: include application of the present agricultural composition to the plant bodies of useful plants, such as foliage application; application of the present agricultural composition to a field in which useful plants are planted or are to be planted, such as a soil treatment; and application of the present agricultural composition to seeds, such as seed sterilization.
The applied amount of the agricultural composition of the present invention differs depending on a climatic condition, a dosage form, an application period, an application method, an application site, a target disease, target crops, etc. In terms of the weight of the present compound contained in the agricultural composition of the present invention, the applied amount is generally between 1 and 500 g, and preferably 2 and 200 g, per 10 ares. An emulsion, a wettable powder, a suspension, etc. are generally diluted with water for application. In such a case, the concentration of the present compound after dilution is generally between 0.0005% and 2% by weight, and preferably between 0.005% and 1% by weight. On the other hand, a powder, a granule, etc. are directly applied without being diluted. When the agricultural composition of the present invention is applied to seeds, the present compound contained in the agricultural composition of the present invention is applied within a range generally between 0.001 and 100 g, and preferably between 0.01 and 50 g, per kg of seeds.
The agricultural composition of the present invention can be used as a reagent for controlling plant diseases caused by plant pathogenic microbes in agricultural lands such as fields, paddy fields, lawns, or orchards. The agricultural composition of the present invention is able to control or prevent plant diseases caused by plant pathogenic microbes in agricultural lands for cultivating the following “crops.”
Examples of the crops are as follows:
crops: corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, peanut, buckwheat, beet, rapeseed, sunflower, sugar cane, tobacco, etc.; vegetables: solanaceous vegetables (eggplant, tomato, pimento, pepper, potato, etc.), cucurbitaceous vegetables (cucumber, pumpkin, zucchini, water melon, melon, etc.), cruciferous vegetables (Japanese radish, white turnip, horseradish, kohlrabi, Chinese cabbage, cabbage, leaf mustard, broccoli, cauliflower, etc.), asteraceous vegetables (burdock, crown daisy, artichoke, lettuce, etc.), liliaceous vegetables (green onion, onion, garlic, and asparagus), ammiaceous vegetables (carrot, parsley, celery, parsnip, etc.), chenopodiaceous vegetables (spinach, Swiss chard, etc.), lamiaceous vegetables (Perilla frutescens, mint, basil, etc.), strawberry, sweet potato, Dioscorea japonica, colocasia, etc.,
flowers;
foliage plants;
fruits: pomaceous fruits (apple, pear, Japanese pear, Chinese quince, quince, etc.), stone fleshy fruits (peach, plum, nectarine, Prunus mume, cherry fruit, apricot, prune, etc.), citrus fruits (Citrus unshiu, orange, lemon, rime, grapefruit, etc.), nuts (chestnuts, walnuts, hazelnuts, almond, pistachio, cashew nuts, macadamia nuts, etc.), berries (blueberry, cranberry, blackberry, raspberry, etc.), grape, kaki fruit, olive, Japanese plum, banana, coffee, date palm, coconuts, etc.,
trees other than fruit trees; tea, mulberry, flowering plant, roadside trees (ash, birch, dogwood, Eucalyptus, Ginkgo biloba, lilac, maple, Quercus, poplar, Judas tree, Liquidambar formosana, plane tree, zelkova, Japanese arborvitae, fir wood, hemlock, juniper, Pinus, Picea, and Taxus cuspidate), etc.
The aforementioned “crops” include crops, to which resistance to HPPD inhibitors such as isoxaflutole, ALS inhibitors such as imazethapyr or thifensulfuron-methyl, EPSP synthetase inhibitors, glutamine synthetase inhibitors, and herbicides such as bromoxynil, has been imparted by a classical breeding method or genetic recombination.
Examples of “crops” to which resistance is imparted by a classical breeding method include Clearfield (registered trademark) canola that is resistant to imidazolinone herbicides such as imazethapyr, and STS soybean that is resistant to sulfonylurea ALS inhibitory herbicides such as thifensulfuron-methyl. In addition, examples of “crops” to which resistance is imparted by genetic recombination include corn varieties resistant to glyphosate or glufosinate. Such corn varieties have already been on the market with product names such as “RoundupReady (registered trademark)” and “LibertyLink (registered trademark).”
The aforementioned “crops” include genetically recombinant crops produced using such genetic recombination techniques, which, for example, are able to synthesize selective toxins as known in genus Bacillus.
Examples of toxins expressed in such genetically recombinant crops include insecticidal proteins derived from Bacillus cereus or Bacillus popilliae; δ-endotoxins such as Cry1Ab, Cry1Ac, Cry1F, Cry1Fa2, Cry2Ab, Cry3A, Cry3Bb1 or Cry9C, derived from Bacillus thuringiensis; insecticidal proteins such as VIP1, VIP2, VIP3, or VIP3A; insecticidal proteins derived from nematodes; toxins generated by animals, such as scorpion toxin, spider toxin, bee toxin, or insect-specific neurotoxins; mold fungi toxins; plant lectin; agglutinin; protease inhibitors such as a trypsin inhibitor, a serine protease inhibitor, patatin, cystatin, or a papain inhibitor; ribosome-inactivating proteins (RIP) such as lycine, corn-RIP, abrin, luffin, saporin, or briodin; steroid-metabolizing enzymes such as 3-hydroxysteroid oxidase, ecdysteroid-UDP-glucosyl transferase, or cholesterol oxidase; an ecdysone inhibitor; HMG-COA reductase; ion channel inhibitors such as a sodium channel inhibitor or calcium channel inhibitor; juvenile hormone esterase; a diuretic hormone receptor; stilbene synthase; bibenzyl synthase; chitinase; and glucanase.
Moreover, toxins expressed in such genetically recombinant crops also include: hybrid toxins of δ-endotoxin proteins such as Cry1Ab, Cry1Ac, Cry1F, Cry1Fa2, Cry2Ab, Cry3A, Cry3Bb1 or Cry9C, and insecticidal proteins such as VIP1, VIP2, VIP3 or VIP3A; partially deleted toxins; and modified toxins. Such hybrid toxins are produced from a new combination of the different domains of such proteins, using a genetic recombination technique. As a partially deleted toxin, Cry1Ab comprising a deletion of a portion of an amino acid sequence has been known. A modified toxin is produced by substitution of one or multiple amino acids of natural toxins.
Examples of such toxins and recombinant plants capable of synthesizing such toxins are described in EP-A-0 374 753, WO 93/07278, WO 95/34656, EP-A-0 427 529, EP-A-451 878, WO 03/052073, etc.
Toxins contained in such recombinant plants are able to impart resistance particularly to insect pests belonging to Coleoptera, Diptera and Lepidoptera, to the plants.
Furthermore, genetically recombinant plants, which comprise one or multiple insecticidal pest-resistant genes and which express one or multiple toxins, have already been known, and some of such genetically recombinant plants have already been on the market. Examples of such genetically recombinant plants include YieldGard (registered trademark) (a corn variety for expressing Cry1Ab toxin), YieldGard Rootworm (registered trademark) (a corn variety for expressing Cry3Bb1 toxin), YieldGard Plus (registered trademark) (a corn variety for expressing Cry1Ab and Cry3Bb1 toxins), Herculex I (registered trademark) (a corn variety for expressing phosphinotricine N-acetyl transferase (PAT) so as to impart resistance to Cry1 Fa2 toxin and gluphosinate), NuCOTN33B (a cotton variety for expressing Cry1Ac toxin), Bollgard I (registered trademark) (a cotton variety for expressing Cry1Ac toxin), Bollgard II (registered trademark) (a cotton variety for expressing CrylAc and Cry2Ab toxins), VIPCOT (registered trademark) (a cotton variety for expressing VIP toxin), NewLeaf (registered trademark) (a potato variety for expressing Cry3A toxin), NatureGard (registered trademark) Agrisure (registered trademark) GT Advantage (GA21 glyphosate-resistant trait), Agrisure (registered trademark) CB Advantage (Bt11 corn borer (CB) trait), and Protecta (registered trademark).
The aforementioned “crops” also include crops produced using a genetic recombinant technique, which have ability to generate antipathogenic substances having selective action.
A PR protein and the like have been known as such antipathogenic substances (PRPs, EP-A-0 392 225). Such antipathogenic substances and genetically recombinant crops that generate them are described in EP-A-0 392 225, WO 95/33818, EP-A-0 353 191, etc.
Examples of such antipathogenic substances expressed in genetically recombinant crops include: ion channel inhibitors such as a sodium channel inhibitor or a calcium channel inhibitor (KP1, KP4 and KP6 toxins, etc., which are produced by viruses, have been known); stilbene synthase; bibenzyl synthase; chitinase; glucanase; a PR protein; and antipathogenic substances generated by microorganisms, such as a peptide antibiotic, an antibiotic having a hetero ring, a protein factor associated with resistance to plant diseases (which is called a plant disease-resistant gene and is described in WO 03/000906).
Examples of plant diseases that can be controlled by the present invention include plant diseases caused by plant pathogenic microbes. More specific examples include the following plant diseases, but examples are not limited thereto.
Magnaporthe grisea, Cochliobolus miyabeanus, Rhizoctonia solani, Gibberella fujikuroi and Sclerophthora macrospora; Erysiphe graminis, Fusarium graminearum, F. avenacerum, F. culmorum, Microdochium nivale, Puccina striiformis, P. graminis, P. recondita, P. hordei, Typhula sp., Micronectriella nivalis, Ustilago tritici, U. nuda, Tilletia caries, Pseudocercosporella herpotrichoides, Rhynchosporium secalis, Septoria tritici, Leptosphaeria nodorum, Pyrenophora teres Drechsler, Gaeumannomyces graminis and Pyrenophoratritici-repentis; Diaporthe citri, Elsinoe fawcetti, Penicillium digitatum and P. italicum; Monilinia mali, Valsa ceratosperma, Podosphaera leucotricha, Alternaria alternata apple pathotype, Venturia inaequalis and Glomerella cingulata; Venturia nashicola, V. pirina, Alternaria alternata Japanese pear pathotype and Gymnosporangium haraeanum; Monilinia fructicola, Cladosporium carpophilum and Phomopsis sp.; Elsinoe ampelina, Glomerella cingulata, Uncinula necator, Phakopsora ampelopsidis, Guignardia bidwellii and Plasmopara viticola; Gloeosporium kaki, Cercospora kaki and Mycosphaerella nawae; Colletotrichum lagenarium, Sphaerotheca fuliginea, Mycosphaerella melonis, Fusarium oxysporum, Pseudoperonospora cubensis, Phytophthora sp. and Pythium sp.; Alternaria solani, Cladosporium fulvum and Phytophthora infestans; Phomopsis vexans and Erysiphe cichoracearum; Alternaria japonica, Cercosporella brassicae, Plasmodiophora brassicae and Peronospora parasitica; Puccinia allii, Cercospora kikuchii, Elsinoe glycines, Diaporthe phaseolorum var. sojae, Phakopsora pachyrhizi, Colletotrichum lindemthianum, Cercospora personata, Cercospora arachidicola and Sclerotium rolfsii; Erysiphe pisi; Alternaria solani, Phytophthora infestans, Verticillium albo-atrum, V. dahliae and V. nigrescens; Sphaerotheca humuli; Exobasidium reticulatum; Elsinoe leucospila, Pestalotiopsis sp., Colletotrichum theae-sinensis, Alternaria longipes, Erysiphe cichoracearum, Colletotrichum tabacum, Peronospora tabacina and Phytophthora nicotianae; Cercospora beticola, Thanatephorus cucumeris, Thanatephorus cucumeris and Aphanomyces sochlioides; Diplocarpon rosae and Sphaerotheca pannosa; Septoria chrysanthemi-indici and Puccinia horiana; Botrytis cinerea, B. byssoidea, B. squamosa and Botrytis alli; Botrytis squamosa, Botrytis cinerea and Sclerotinia sclerotiorum; Alternaria brassicicola; Sclerotinia homeocarpa and Rhizoctonia solani; Hemileia vastatrix; and Mycosphaerella fijiensis and Mycosphaerella musicola.
Next, the present invention will be more specifically described in the following examples such as production examples, formulation examples, and test examples. However, these examples are not intended to limit the scope of the present invention.
1.80 g of 2-chloronicotinic acid chloride, 1.20 g of benzylamine, and 1.50 g of triethylamine were added to 5 ml of THF. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was concentrated, and the obtained residue was then subjected to silica gel column chromatography, so as to obtain 2.50 g of N-phenylmethyl-2-chloronicotinic acid amide.
1H-NMR (CDCl3) δ: 4.62 (2H, d, J=5.6 Hz), 6.95 (1H, br s), 7.25-7.40 (6H, m), 8.03 (1H, dd, J=7.7, 1.9 Hz), 8.39 (1H, dd, J=4.8, 1.9 Hz).
0.50 g of N-phenylmethyl-2-chloronicotinic acid amide and 1 ml of 1,4-dioxane were added to 4 ml of 28% aqueous ammonia. The obtained mixture was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 140° C. for 2 hours. After, water was added to the reaction mixture, it was then extracted with chloroform. The organic layer was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.36 g of N-phenylmethyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 1).
The present compound 1
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.8 Hz), 6.27-6.48 (3H, br m), 6.56 (1H, dd, J=7.7, 4.8 Hz), 7.28-7.38 (5H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.14 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.27 g of 2-aminonicotinic acid, 0.30 g of 1-hydroxybenzotriazole, 0.40 g of WSC, 0.25 g of 4-fluorobenzylamine and 10 ml of DMF was stirred at 100° C. for 5 minutes, and then at a room temperature for 1 hour. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.30 g of N-(4-fluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 2).
The present compound 2
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.9 Hz), 6.29-6.41 (3H, br m), 6.58 (1H, dd, J=7.7, 4.9 Hz), 7.01-7.08 (2H, m), 7.29-7.34 (2H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.88 g of a BOP reagent and 0.40 g of triethylamine were successively added to a mixture of 0.28 g of 2-aminonicotinic acid, 0.40 g of 4-phenoxybenzylamine and 10 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure.
0.80 g of the obtained residue was subjected to silica gel column chromatography, so as to obtain 0.62 g of N-(4-phenoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 3).
The present compound 3
1H-NMR (DMSO-D6) δ: 4.42 (2H, d, J=5.9 Hz), 6.59 (1H, dd, J=7.8, 4.9 Hz), 6.97-6.99 (4H, m), 7.08 (2H, br), 7.10-7.13 (1H, m), 7.32-7.40 (4H, m), 7.95 (1H, dd, J=7.8, 1.7 Hz), 8.08 (1H, dd, J=4.9, 1.7 Hz), 8.98 (1H, t, J=5.9 Hz).
0.88 g of a BOP reagent and 0.40 g of triethylamine were successively added to a mixture of 0.28 g of 2-aminonicotinic acid, 0.37 g of 4-phenylbenzylamine and 10 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. 0.71 g of the obtained residue was subjected to silica gel column chromatography, so as to obtain 0.53 g of N-(4-phenylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 4).
The present compound 4
1H-NMR (DMSO-D6) δ: 4.48 (2H, d, J=5.8 Hz), 6.60 (1H, dd, J=7.8, 4.9 Hz), 7.09 (2H, br), 7.33-7.48 (5H, m), 7.62-7.65 (4H, m), 7.98 (1H, dd, J=7.8, 1.5 Hz), 8.09 (1H, m), 9.01-9.04 (1H, m).
0.88 g of a BOP reagent and 0.40 g of triethylamine were successively added to a mixture of 0.28 g of 2-aminonicotinic acid, 0.37 g of 3-phenylbenzylamine and 10 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. 0.77 g of the obtained residue was subjected to silica gel column chromatography, so as to obtain 0.58 g of N-(3-phenylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 5).
The present compound 5
1H-NMR (DMSO-D6) δ: 4.52 (2H, d, J=5.8 Hz), 6.60 (1H, dd, J=7.8, 4.9 Hz), 7.07 (2H, br), 7.31-7.49 (5H, m), 7.53-7.55 (1H, m), 7.61-7.65 (3H, m), 7.97 (1H, dd, J=7.8, 2.0 Hz), 8.07-8.09 (1H, m), 9.01-9.04 (1H, m).
0.88 g of a BOP reagent and 0.40 g of triethylamine were successively added to a mixture of 0.28 g of 2-aminonicotinic acid, 0.43 g of 3-benzyloxybenzylamine and 10 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. 0.87 g of the obtained residue was subjected to silica gel column chromatography, so as to obtain 0.70 g of N-(3-benzyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 7).
The present compound 7
1H-NMR (DMSO-D6) δ: 4.40 (2H, d, J=5.9 Hz), 5.08 (2H, s), 6.58-6.60 (1H, m), 6.87-6.89 (2H, m), 6.95 (1H, br), 7.06 (2H, br), 7.24 (1H, t, J=7.2 Hz), 7.29-7.38 (3H, m), 7.42-7.44 (2H, m), 7.93-7.95 (1H, m), 8.07-8.08 (1H, m), 8.94-8.97 (1H, m).
0.88 g of a BOP reagent and 0.40 g of triethylamine were successively added to a mixture of 0.28 g of 2-aminonicotinic acid, 0.27 g of 3-methoxybenzylamine and 7 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture and it was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. 0.62 g of the obtained residue was subjected to silica gel column chromatography, so as to obtain 0.52 g of N-(3-methoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 8).
The present compound 8
1H-NMR (DMSO-D6) δ: 3.73 (3H, s), 4.41 (2H, d, J=5.9 Hz), 6.58-6.61 (1H, m), 6.80-6.83 (1H, m), 6.87-6.95 (2H, m), 7.06 (2H, br), 7.22-7.26 (1H, m), 7.95 (1H, dd, J=7.6, 1.7 Hz), 8.08 (1H, dd, J=4.6, 1.4 Hz), 8.96 (1H, t, J=5.9 Hz).
A mixture of 0.18 g of 2-aminonicotinic acid, 0.18 g of 4-methoxybenzylamine, 0.33 g of WSC and 5 ml of pyridine was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.14 g of N-(4-methoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 9).
The present compound 9
1H-NMR (CDCl3) δ: 3.81 (3H, s), 4.53 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.88-6.91 (2H, m), 7.25-7.29 (2H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.18 g of 4-pentylbenzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and MTBE. The resultant was dried, so as to obtain 0.29 g of N-(4-pentylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 10).
The present compound 10
1H-NMR (CDCl3) δ: 0.88-0.91 (3H, m), 1.28-1.35 (4H, m), 1.58-1.68 (2H, m), 2.58-2.62 (2H, m), 4.56 (2H, d, J=5.7 Hz), 6.23 (1H, br), 6.36 (2H, br), 6.57 (1H, dd, J=7.8, 4.9 Hz), 7.14-7.19 (2H, m), 7.21-7.27 (2H, m), 7.58 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.18 g of 3-pentylbenzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and cold MTBE. The resultant was dried, so as to obtain 0.15 g of N-(3-pentylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 11).
The present compound 11
1H-NMR (CDCl3) δ: 0.87-0.91 (3H, m), 1.28-1.38 (4H, m), 1.55-1.65 (2H, m), 2.58-2.63 (2H, m), 4.58 (2H, d, J=5.6 Hz), 6.25 (1H, br), 6.36 (2H, br), 6.57-6.60 (1H, m), 7.12-7.16 (3H, m), 7.26-7.30 (1H, m), 7.58 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.50 g of 2,6-diaminonicotinic acid, 0.53 g of 1-hydroxybenzotriazole, 0.75 g of WSC, 0.49 g of 2-fluorobenzylamine and 10 ml of DMF was stirred at a room temperature for 8 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.30 g of N-(2-fluorophenyl)methyl-2,6-diaminonicotinic acid amide (hereinafter referred to as the present compound 12).
The present compound 12
1H-NMR (CDCl3) δ: 4.50 (2H, br s), 4.62 (2H, d, J=5.8 Hz), 5.78 (1H, dd, J=8.5, 0.5 Hz), 6.11-6.14 (1H, br m), 6.42 (2H, br s), 7.03-7.14 (2H, m), 7.24-7.30 (1H, m), 7.36-7.42 (2H, m).
A mixture of 0.53 g of 2,6-diaminonicotinic acid, 0.59 g of 1-hydroxybenzotriazole, 0.79 g of WSC, 0.77 g of 2-fluoro-3-methoxybenzylamine hydrochloride, 2 ml of triethylamine and 3 ml of DMF was stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The solid was successively washed with a sodium hydroxide aqueous solution, water and hexane, so as to obtain 0.35 g of N-(2-fluoro-3-methoxyphenyl)methyl-2,6-diaminonicotinic acid amide (hereinafter referred to as the present compound 13).
The present compound 13
1H-NMR (CDCl3) δ: 3.89 (3H, s), 4.51 (2H, br s), 4.61 (2H, d, J=5.9 Hz), 5.77 (1H, d, J=8.3 Hz), 6.15 (1H, br s), 6.42 (2H, br s), 6.88-6.97 (2H, m), 7.02-7.06 (1H, m), 7.38 (1H, d, J=8.3 Hz).
A mixture of 0.50 g of 2,6-diaminonicotinic acid, 0.53 g of 1-hydroxybenzotriazole, 0.75 g of WSC, 0.93 g of 3-phenoxybenzylamine hydrochloride and 10 ml of DMF was stirred at a room temperature for 8 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.52 g of N-(3-phenoxyphenyl)methyl-2,6-diaminonicotinic acid amide (hereinafter referred to as the present compound 15).
The present compound 15
1H-NMR (CDCl3) δ: 4.53 (2H, d, J=5.6 Hz), 4.61 (2H, br s), 5.76 (1H, d, J=8.5 Hz), 6.13-6.20 (1H, br m), 6.46 (2H, br s), 6.87-6.91 (1H, m), 6.96-7.13 (5H, m), 7.28-7.40 (4H, m).
A mixture of 1.0 g of 2,6-diaminonicotinic acid, 0.81 g of 1-hydroxybenzotriazole, 1.2 g of WSC, 1.0 g of 4-(4-fluorophenyloxy)benzylamine and 5 ml of pyridine was stirred under heating to reflux for 10 minutes, and then at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 1.2 g of N-[4-(4-fluorophenyloxy)phenyl]methyl-2,6-diaminonicotinic acid amide (hereinafter referred to as the present compound 16).
The present compound 16
1H-NMR (CDCl3) δ: 4.52 (2H, br s), 4.53 (2H, d, J=5.6 Hz), 5.77 (1H, d, J=8.5 Hz), 6.03 (1H, br s), 6.45 (2H, br s), 6.92-7.05 (6H, m), 7.29 (2H, d, J=8.8 Hz), 7.38 (1H, d, J=8.5 Hz).
A mixture of 0.50 g of 2,6-diaminonicotinic acid, 0.57 g of 1-hydroxybenzotriazole, 0.82 g of WSC, 0.65 g of 4-phenoxybenzylamine, 0.50 g of triethylamine and 4 ml of DMF was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.37 g of N-(4-phenoxyphenyl)methyl-2,6-diaminonicotinic acid amide (hereinafter referred to as the present compound 17).
The present compound 17
1H-NMR (CDCl3) δ: 4.50 (2H, br s), 4.54 (2H, d, J=5.6 Hz), 5.78 (1H, dd, J=8.5, 1.2 Hz), 6.02 (1H, br s), 6.45 (2H, br s), 6.97-7.02 (4H, m), 7.08-7.13 (1H, m), 7.29-7.40 (5H, m).
A mixture of 0.28 g of 2-fluoro-3-methoxybenzylamine hydrochloride, 0.20 g of 2-aminonicotinic acid, 0.35 g of WSC and 3 ml of pyridine was stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The solid was successively washed with a sodium hydroxide aqueous solution, water and hexane, so as to obtain 0.16 g of N-(2-fluoro-3-methoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 18).
The present compound 18
1H-NMR (DMSO-D6) δ: 3.83 (3H, s), 4.46 (2H, d, J=5.6 Hz), 6.57-6.62 (1H, m), 6.88-6.91 (1H, m), 7.01-7.11 (4H, m), 7.93-7.96 (1H, m), 8.05-8.09 (1H, m), 8.93-8.98 (1H, m).
A mixture of 0.45 g of 2,6-difluoronicotinic acid, 0.49 g of 1-hydroxybenzotriazole, 0.69 g of WSC, 0.60 g of 4-(4-fluorophenoxy)benzylamine and 4 ml of pyridine was stirred under heating to reflux for 10 minutes, and then at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.80 g of N-[4-(4-fluorophenoxy)phenyl]methyl-2,6-difluoronicotinic acid amide. N-[4-(4-fluorophenoxy)phenyl]methyl-2,6-difluoronicotinic acid amide
1H-NMR (CDCl3) δ: 4.64 (2H, d, J=5.1 Hz), 6.92-7.09 (8H, m), 7.28-7.35 (2H, m), 8.67-8.78 (1H, m).
700 mg of N-[4-(4-fluorophenoxy)phenyl]methyl-2,6-difluoronicotinic acid amide was added to 2 ml of 28% aqueous ammonia. The obtained mixture was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 100° C. for 10 minutes. The reaction mixture was concentrated under reduced pressure, and the obtained residue was then subjected to silica gel column chromatography, so as to obtain 181 mg of N-[4-(4-fluorophenoxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 19), 216 mg of N-[4-(4-fluorophenoxy)phenyl]methyl-6-amino-2-fluoronicotinic acid amide and 124 mg of N-[4-(4-fluorophenoxy)phenyl]methyl-2,6-diaminofluoronicotinic acid amide.
The present compound 19
1H-NMR (CDCl3) δ: 4.55 (2H, d, J=5.6 Hz), 6.15 (1H, dd, J=8.3, 2.9 Hz), 6.18 (1H, br s), 6.61 (2H, br s), 6.93-7.06 (6H, m), 7.28-7.31 (2H, m), 7.68 (1H, dd, J=8.0, 8.3 Hz). N-[4-(4-fluorophenyloxy)phenyl]methyl-6-amino-2-fluoronicotinic acid amide
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.1 Hz), 4.88 (2H, br s), 6.42 (1H, dd, J=8.3, 2.7 Hz), 6.93-7.05 (7H, m), 7.29-7.32 (2H, m), 8.32 (1H, dd, J=10.2, 8.3 Hz).
A mixture of 0.40 g of 2-aminonicotinic acid, 0.51 g of 1-hydroxybenzotriazole, 0.72 g of WSC, 0.62 g of 3-(3-methylphenoxy)benzylamine and 4 ml of DMF was stirred under heating to reflux for 15 minutes, and then at a room temperature for 4 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with a sodium bicarbonate aqueous solution and water, and it was then dried under reduced pressure, so as to obtain 0.58 g of N-[3-(3-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 20).
The present compound 20
1H-NMR (CDCl3) δ: 2.32 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.34 (2H, br s), 6.42 (1H, br s), 6.54-6.60 (1H, m), 6.79-6.84 (2H, m), 6.89-7.07 (4H, m), 7.19-7.32 (2H, m), 7.57-7.60 (1H, m), 8.14 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.40 g of 2-aminonicotinic acid, 0.51 g of 1-hydroxybenzotriazole, 0.72 g of WSC, 0.62 g of 4-(4-methylphenoxy)benzylamine and 4 ml of DMF was stirred under heating to reflux for 15 minutes, and then at a room temperature for 4 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with a sodium bicarbonate aqueous solution and water, and it was then dried under reduced pressure, so as to obtain 0.80 g of N-[4-(4-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 21).
The present compound 21
1H-NMR (CDCl3) δ: 2.33 (3H, s), 4.55 (2H, d, J=4.8 Hz), 6.30-6.39 (3H, br m), 6.57 (1H, dd, J=7.2, 5.1 Hz), 6.91 (2H, d, J=8.5 Hz), 6.96 (2H, d, J=8.5 Hz), 7.14 (2H, d, J=8.7 Hz), 7.25-7.34 (2H, m), 7.57-7.61 (1H, m), 8.14-8.16 (1H, m).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.21 g of 3-(phenoxymethyl)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and cold MTBE. The resultant was dried, so as to obtain 0.23 g of N-[3-(phenoxymethyl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 22).
The present compound 22
1H-NMR (CDCl3) δ: 4.62 (2H, d, J=5.4 Hz), 5.07 (2H, s), 6.36 (3H, br), 6.56-6.59 (1H, m), 6.96-6.98 (3H, m), 7.29-7.41 (6H, m), 7.56-7.58 (1H, m), 8.15-8.16 (1H, m).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.21 g of 4-(phenoxymethyl)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and cold MTBE. The resultant was dried, so as to obtain 0.34 g of N-[4-(phenoxymethyl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 23).
The present compound 23
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.6 Hz), 5.07 (2H, s), 6.30 (1H, br), 6.36 (2H, br), 6.58 (1H, dd, J=7.9, 4.9 Hz), 6.96-6.98 (3H, m), 7.27-7.45 (6H, m), 7.58-7.60 (1H, m), 8.16-8.17 (1H, m).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.21 g of 3-(2-phenylethyl)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.24 g of N-[3-(2-phenylethyl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 24).
The present compound 24
1H-NMR (CDCl3) δ: 2.91 (4H, s), 4.55 (2H, d, J=5.6 Hz), 6.25 (1H, br), 6.37 (2H, br), 6.57-6.60 (1H, m), 7.10-7.30 (9H, m), 7.56 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.21 g of 4-(2-phenylethyl)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture. The obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and cold MTBE. The resultant was dried, so as to obtain 0.24 g of N-[4-(2-phenylethyl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 25).
The present compound 25
1H-NMR (CDCl3) δ: 2.88-2.99 (4H, m), 4.57 (2H, d, J=5.4 Hz), 6.25 (1H, br), 6.36 (2H, br), 6.56-6.59 (1H, m), 7.18-7.30 (9H, m), 7.57-7.59 (1H, m), 8.15-8.16 (1H, m).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.23 g of 3-(2-phenylethyloxy)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.24 g of N-[3-(2-phenylethoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 26).
The present compound 26
1H-NMR (CDCl3) δ: 3.07-3.10 (2H, m), 4.17 (2H, t, J=7.1 Hz), 4.54 (2H, d, J=5.4 Hz), 6.36 (3H, br), 6.56 (1H, dd, J=7.9, 4.9 Hz), 6.81-6.90 (3H, m), 7.21-7.32 (6H, m), 7.58 (1H, dd, J=7.9, 1.7 Hz), 8.13 (1H, dd, J=4.9, 1.7 Hz).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.23 g of 4-(2-phenylethyloxy)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and 30 ml of water were added to the reaction mixture. The obtained mixture was stirred at a room temperature for 30 minutes, and then under cooling on ice for 30 minutes. Thereafter, the precipitated solid was collected by filtration, and it was then successively washed with water and cold MTBE. The resultant was dried, so as to obtain 0.28 g of N-[4-(2-phenylethoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 27).
The present compound 27
1H-NMR (CDCl3) δ: 3.08-3.12 (2H, m), 4.15-4.19 (2H, m), 4.52 (2H, d, J=5.4 Hz), 6.19 (1H, br), 6.35 (2H, br), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.87-6.90 (2H, m), 7.22-7.34 (7H, m), 7.56 (1H, dd, J=7.8, 1.7 Hz), 8.15-8.16 (1H, m).
0.50 g of 2-chloro-6-methyl-nicotinic acid, 0.64 g of 4-phenoxybenzylamine and 0.64 g of WSC were mixed with 5 ml of DMF. The obtained mixture was stirred under heating at 100° C. for 5 minutes, and it was then stirred at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.60 g of N-(4-phenoxyphenyl)methyl-2-chloro-6-methyl-nicotinic acid amide.
1H-NMR (CDCl3) δ: 2.57 (3H, s), 4.64 (2H, d, J=5.8 Hz), 6.87 (1H, br s), 6.98-7.02 (4H, m), 7.09-7.13 (1H, m), 7.20 (1H, d, J=7.7 Hz), 7.31-7.37 (4H, m), 8.09 (1H, d, J=7.7 Hz).
0.30 g of the thus obtained N-(4-phenoxyphenyl)methyl-2-chloro-6-methyl-nicotinic acid amide, 1 ml of 1,4-dioxane and 3 ml of 28% aqueous ammonia were mixed. The obtained mixture was subjected to a microwave reactor at 100° C. for 3 hours to react. The reaction mixture was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.13 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methyl-nicotinic acid amide (hereinafter referred to as the present compound 29).
The present compound 29
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.38 (2H, br s), 6.44 (1H, d, J=8.0 Hz), 6.98-7.02 (4H, m), 7.09-7.13 (1H, m), 7.28-7.36 (4H, m), 7.49 (1H, d, J=7.7 Hz).
A mixture of 0.20 g of 2-aminonicotinic acid, 0.24 g of 1-hydroxybenzotriazole, 0.34 g of WSC, 0.37 g of 4-fluoro-3-phenoxybenzylamine and 4 ml of DMF was stirred at 50° C. for 8 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.30 g of N-(4-fluoro-3-phenoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 33).
The present compound 33
1H-NMR (CDCl3) δ: 4.50 (2H, d, J=5.6 Hz), 6.34 (2H, br s), 6.49 (1H, br s), 6.55 (1H, dd, J=7.6, 4.9 Hz), 6.95-7.16 (6H, m), 7.29-7.35 (2H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.13 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.20 g of 2-aminonicotinic acid, 0.24 g of 1-hydroxybenzotriazole, 0.34 g of WSC, 0.38 g of 4-(4-fluorophenoxy)benzylamine and 4 ml of DMF was stirred at a room temperature for 8 hours, and then at 80° C. for 2 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.50 g of N-[4-(4-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 34).
The present compound 34
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.93-7.06 (6H, m), 7.30 (2H, d, J=8.8 Hz), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.44 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.19 g of 2-aminomethyl-5-phenoxyfuran and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, ice and a saline solution were successively added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was further washed with a saline solution 3 times, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.27 g of N-(5-phenoxyfuran-2-yl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 35).
The present compound 35
1H-NMR (CDCl3) δ: 4.52 (2H, d, J=5.4 Hz), 5.51 (1H, d, J=2.9 Hz), 6.27 (1H, d, J=2.9 Hz), 6.31 (3H, br), 6.59 (1H, dd, J=7.6, 4.9 Hz), 7.04-7.06 (2H, m), 7.12-7.15 (1H, m), 7.32-7.36 (2H, m), 7.59-7.60 (1H, m), 8.16-8.17 (1H, m).
A mixture of 2.0 g of 2-aminonicotinic acid, 2.0 g of 1-hydroxybenzotriazole, 4.1 g of WSC, 4.0 g of (2-chlorothiazol-5-yl)methylamine hydrobromide, 5.0 g of triethylamine and 20 ml of DMF was stirred at 50° C. for 3 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.20 g of N-(2-chlorothiazol-5-yl)methyl-2-aminonicotinic acid amide.
1H-NMR (CDCl3) δ: 4.68 (2H, dd, J=5.9, 0.8 Hz), 6.36 (2H, br s), 6.47 (1H, br s), 6.60 (1H, dd, J=7.8, 4.8 Hz), 7.45 (1H, s), 7.58 (1H, dd, J=7.8, 1.8 Hz), 8.19 (1H, dd, J=4.8, 1.8 Hz).
0.70 g of N-(2-chlorothiazol-5-yl)methyl-2-aminonicotinic acid amide, 1.40 g of benzyl alcohol, and 1.2 g of potassium 1,1-dimethylethoxide were added to 20 ml of 1,2-dimethoxyethane. The obtained mixture was heated to reflux for 4 hours. After, water was added to the reaction mixture, the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.13 g of N-(2-benzyloxythiazol-5-yl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 43).
The present compound 43
1H-NMR (CDCl3) δ: 4.61 (2H, dd, J=5.8, 0.7 Hz), 5.41 (2H, s), 6.27-6.37 (3H, br m), 6.59 (1H, dd, J=7.7, 4.8 Hz), 7.05 (1H, s), 7.35-7.45 (5H, m), 7.56 (1H, dd, J=7.7, 1.7 Hz), 8.17 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.30 g of 2-aminonicotinic acid, 0.30 g of 1-hydroxybenzotriazole, 0.63 g of WSC, 0.60 g of 2-butoxythiazol-5-ylmethylamine and 4 ml of DMF was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.53 g of N-(2-butoxythiazol-5-yl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 44).
The present compound 44
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.4 Hz), 1.41-1.50 (2H, m), 1.73-1.81 (2H, m), 4.36 (2H, t, J=6.6 Hz), 4.60 (2H, dd, J=5.6, 0.7 Hz), 6.31-6.40 (3H, br m), 6.58 (1H, dd, J=7.8, 4.8 Hz), 7.01 (1H, s), 7.58 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 1.0 g of 2,6-difluoronicotinic acid, 1.4 g of WSC, 1.4 g of 4-phenoxybenzylamine and 5 ml of DMF was stirred at a room temperature for 2 days. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.90 g of N-(4-phenoxyphenyl)methyl-2,6-difluoronicotinic acid amide.
1H-NMR (CDCl3) δ: 4.64 (2H, d, J=5.4 Hz), 6.97-7.03 (6H, m), 7.09-7.14 (1H, m), 7.30-7.36 (4H, m), 8.69-8.76 (1H, m).
A mixture of 0.90 g of N-(4-phenoxyphenyl)methyl-2,6-difluoronicotinic acid amide, 1 ml of 1,4-dioxane and 1 ml of 28% aqueous ammonia was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 80° C. for 10 minutes. After the reaction, the reaction mixture was concentrated under reduced pressure, the obtained residue was subjected to silica gel column chromatography, so as to obtain 205 mg of N-(4-phenoxyphenyl)methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 46), 191 mg of N-(4-phenoxyphenyl)methyl-6-amino-2-fluoronicotinic acid amide and 155 mg of N-(4-phenoxyphenyl)methyl-2,6-diaminonicotinic acid amide.
The present compound 46
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.13-6.19 (1H, br m), 6.15 (1H, dd, J=8.2, 2.7 Hz), 6.61 (2H, br s), 6.98-7.02 (4H, m), 7.09-7.14 (1H, m), 7.28-7.37 (4H, m), 7.69 (1H, t, J=8.1 Hz).
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.1 Hz), 4.88 (2H, br s), 6.42 (1H, dd, J=8.2, 2.7 Hz), 6.92-7.04 (5H, m), 7.07-7.13 (1H, m), 7.30-7.35 (4H, m), 8.32 (1H, dd, J=10.3, 8.3 Hz).
A mixture of 0.50 g of 4-(2-methoxyphenoxy)benzylamine, 0.25 g of 2-aminonicotinic acid, 0.25 g of 1-hydroxybenzotriazole, 0.50 g of WSC and 4 ml of DMF was stirred at 140° C. for 4 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.34 g of N-[4-(2-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 47).
The present compound 47
1H-NMR (CDCl3) δ: 3.84 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.90-7.03 (5H, m), 7.15 (1H, ddd, J=8.5, 6.8, 1.4 Hz), 7.24-7.28 (2H, m), 7.58 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.8, 1.8 Hz).
2.0 g of 4-(3-methoxyphenoxy)benzonitrile and 0.50 g of lithium aluminum hydride were added to 40 ml of THF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then left at a room temperature overnight. Thereafter, the reaction mixture was filtrated with Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE was added to the residue, and potassium carbonate was then added to the mixture. The obtained mixture was dried, and it was then filtrated with Celite (registered trade mark). The filtrate was concentrated under reduced pressure, so as to obtain 1.8 g of crude 4-(3-methoxyphenoxy)benzylamine.
A mixture of 0.50 g of the thus obtained crude 4-(3-methoxyphenoxy)benzylamine, 0.25 g of 2,-aminonicotinic acid, 0.25 g of 1-hydroxybenzotriazole, 0.50 g of WSC and 4 ml of DMF was stirred at 140° C. for 4 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.49 g of N-[4-(3-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 48).
The present compound 48
1H-NMR (CDCl3) δ: 3.78 (3H, s), 4.57 (2H, d, J=5.6 Hz), 6.31-6.42 (3H, br m), 6.56-6.60 (3H, m), 6.64-6.68 (1H, m), 6.98-7.03 (2H, m), 7.20-7.25 (1H, m), 7.29-7.32 (2H, m), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=5.0, 1.8 Hz).
2.0 g of 4-(4-methoxyphenoxy)benzonitrile and 0.5 g of lithium aluminum hydride were added to 40 ml of THF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then left at a room temperature overnight. Thereafter, the reaction mixture was filtrated with Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE was added to the residue, and potassium carbonate was then added to the mixture. The obtained mixture was dried, and it was then filtrated with Celite (registered trade mark). The filtrate was concentrated under reduced pressure, so as to obtain 1.9 g of crude 4-(4-methoxyphenoxy)benzylamine.
A mixture of 0.50 g of the thus obtained crude 4-(4-methoxyphenoxy)benzylamine, 0.25 g of 2,-aminonicotinic acid, 0.25 g of 1-hydroxybenzotriazole, 0.50 g of WSC and 4 ml of DMF was stirred at 140° C. for 4 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.29 g of N-[4-(4-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 49).
The present compound 49
1H-NMR (CDCl3) δ: 3.81 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.7, 4.7 Hz), 6.87-7.00 (6H, m), 7.25-7.29 (2H, m), 7.58 (1H, dd, J=7.7, 1.5 Hz), 8.16 (1H, dd, J=4.7, 1.5 Hz).
A mixture of 0.35 g of 3-(2-methoxyphenoxy)benzylamine, 0.20 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.35 g of WSC and 2 ml of DMF was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.47 g of N-[3-(2-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 50).
The present compound 50
1H-NMR (CDCl3) δ: 3.82 (3H, s), 4.56 (2H, d, J=5.8 Hz), 6.29 (1H, br s), 6.33 (2H, br s), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.83 (1H, dd, J=8.2, 1.9 Hz), 6.91-7.02 (5H, m), 7.12-7.18 (1H, m), 7.26 (2H, dd, J=8.1, 7.6 Hz), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 5.4 g of 3-fluorobenzonitrile, 5.8 g of 3-methoxyphenol, 15.9 g of cesium carbonate and 30 ml of DMF was stirred at 140° C. for 3 hours. Thereafter, the reaction mixture solution was cooled to a room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was successively washed with a 15% sodium hydroxide aqueous solution, diluted hydrochloric acid, and a saturated saline solution. The resultant was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 1.1 g of 3-(3-methoxyphenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 3.80 (3H, s), 6.58-6.61 (2H, m), 6.75 (1H, ddd, J=8.4, 2.4, 0.8 Hz), 7.23-7.44 (5H, m).
A mixture of 0.34 g of lithium aluminum hydride and 30 ml of THF was stirred under cooling on ice. A mixture solution of 1.0 g of 3-(3-methoxyphenoxy)benzonitrile and 20 ml of THF was added dropwise to the reaction mixture. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture solution was cooled to 0° C., and 0.3 ml of water, 0.3 ml of 15% sodium hydroxide aqueous solution and 0.9 ml of water were then successively added to the reaction mixture. The mixture was stirred for 1 hour. The mixture was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure, so as to obtain 0.8 g of crude 3-(3-methoxyphenoxy)benzylamine.
A mixture of 0.35 g of the thus obtained crude 3-(3-methoxyphenoxy)benzylamine, 0.20 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.35 g of WSC and 2 ml of DMF was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.36 g of N-[3-(3-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 51).
The present compound 51
1H-NMR (CDCl3) δ: 3.78 (3H, s), 4.58 (2H, d, J=5.6 Hz), 6.30-6.38 (3H, br m), 6.57-6.60 (3H, m), 6.65-6.69 (1H, m), 6.94 (1H, dd, J=7.8, 2.1 Hz), 6.99-7.01 (1H, m), 7.07 (1H, d, J=7.5 Hz), 7.21-7.25 (1H, m), 7.29-7.34 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.9 Hz).
A mixture of 0.35 g of 3-(4-methoxyphenoxy)benzylamine, 0.20 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.35 g of WSC and 2 ml of DMF was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.37 g of N-[3-(4-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 52).
The present compound 52
1H-NMR (CDCl3) δ: 3.81 (3H, s), 4.55 (2H, d, J=5.8 Hz), 6.27-6.37 (3H, br m), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.84-6.91 (4H, m), 6.97-7.02 (3H, m), 7.25-7.29 (1H, m), 7.57 (1H, dd, J=7.7, 1.7 Hz), 8.15-8.17 (1H, m).
1.0 g of 2,6-dichloro-5-fluoronicotinic acid and 1.0 g of thionyl chloride were added to 20 ml of toluene, and the obtained mixture was heated to reflux for 1 hour. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2,6-dichloro-5-fluoronicotinic acid chloride.
The thus obtained crude 2,6-dichloro-5-fluoronicotinic acid chloride was dissolved in 20 ml of THF. A mixture solution of 1.0 g of 4-phenoxybenzylamine, 2.0 g of triethylalmine and 5 ml of THF was then added dropwise to the above obtained solution at 0° C. The obtained solution was stirred at a room temperature for 4 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 1.25 g of N-(4-phenoxyphenyl)methyl-2,6-dichloro-5-fluoronicotinic acid amide.
1H-NMR (CDCl3) δ: 4.64 (2H, d, J=5.6 Hz), 6.90 (1H, br s), 6.98-7.03 (4H, m), 7.10-7.15 (1H, m), 7.30-7.37 (4H, m), 8.04 (1H, d, J=7.5 Hz).
A mixture of 1.0 g of N-(4-phenoxyphenyl)methyl-2,6-dichloro-5-fluoronicotinic acid amide and 2 ml of 28% aqueous ammonia was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 80° C. for 40 minutes. After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 85 mg of N-(4-phenoxyphenyl)methyl-2-amino-6-chloro-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 53) and 600 mg of N-(4-phenoxyphenyl)methyl-6-amino-2-chloro-5-fluoronicotinic acid amide.
The present compound 53
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.16 (1H, br s), 6.38 (2H, br s), 6.98-7.03 (4H, m), 7.10-7.14 (1H, m), 7.27-7.37 (4H, m), 7.42 (1H, d, J=8.0 Hz). N-(4-phenoxyphenyl)methyl-6-amino-2-chloro-5-fluoronicotinic acid amide
1H-NMR (CDCl3) δ: 4.62 (2H, d, J=5.6 Hz), 5.02 (2H, br s), 6.98-7.03 (4H, m), 7.09-7.18 (2H, m), 7.30-7.36 (4H, m), 7.93 (1H, d, J=10.4 Hz).
0.30 g of N-(4-phenoxyphenyl)methyl-6-amino-2-chloro-5-fluoronicotinic acid amide and 0.5 ml of 1,4-dioxane were added to 2 ml of 28% aqueous ammonia. The obtained mixture was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 120° C. for 5 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.22 g of N-(4-phenoxyphenyl)methyl-2,6-diamino-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 54).
The present compound 54
1H-NMR (CDCl3) δ: 4.53 (2H, d, J=5.6 Hz), 4.73 (2H, br s), 5.94 (1H, br s), 6.29 (2H, br s), 6.96-7.02 (4H, m), 7.08-7.13 (1H, m), 7.19 (1H, d, J=10.7 Hz), 7.27-7.37 (4H, m).
A mixture of 0.14 g of 2-aminonicotinic acid, 0.23 g of 4-benzyloxy-2-fluorobenzylamine, 0.25 g of WSC and 3 ml of pyridine was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.15 g of N-(4-benzyloxy-2-fluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 55).
The present compound 55
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 5.05 (2H, s), 6.32 (3H, br s), 6.56-6.60 (1H, m), 6.69-6.76 (2H, m), 7.26-7.41 (6H, m), 7.57 (1H, dd, J=7.7, 1.7 Hz), 8.15 (1H, dd, J=4.6, 1.7 Hz).
A mixture of 0.34 g of sodium {4-[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.19 g of 2-methylbenzyl bromide and 3 ml of DMF was stirred at a room temperature for 2 hours. Subsequently, 0.39 g of cesium carbonate was added thereto, and the obtained mixture was then stirred at a room temperature for 3 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 55 mg of N-[4-(2-methylbenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 58).
The present compound 58
1H-NMR (CDCl3) δ: 2.37 (3H, s), 4.54 (2H, d, J=5.6 Hz), 5.04 (2H, s), 6.22 (1H, br s), 6.36 (2H, br s), 6.56-6.59 (1H, m), 6.96-7.00 (2H, m), 7.20-7.30 (5H, m), 7.38-7.41 (1H, m), 7.56-7.58 (1H, m), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.14 g of 3-methylbenzyl chloride, 0.39 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.16 g of N-[4-(3-methylbenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 59).
The present compound 59
1H-NMR (CDCl3) δ: 2.37 (3H, s), 4.53 (2H, d, J=5.4 Hz), 5.03 (2H, s), 6.20 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.95-6.98 (2H, m), 7.15-7.29 (6H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.14 g of 4-methylbenzyl chloride, 0.39 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.17 g of N-[4-(4-methylbenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 60).
The present compound 60
1H-NMR (CDCl3) δ: 2.36 (3H, s), 4.53 (2H, d, J=5.6 Hz), 5.02 (2H, s), 6.20 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.94-6.97 (2H, m), 7.19 (2H, d, J=7.8 Hz), 7.25-7.27 (2H, m), 7.31 (2H, d, J=7.8 Hz), 7.56 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 1.0 g of 2,6-dichloronicotinic acid, 1.3 g of WSC, 1.3 g of 4-phenoxybenzylamine and 5 ml of DMF was stirred at 100° C. for 4 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.37 g of N-(4-phenoxyphenyl)methyl-2,6-dichloronicotinic acid amide.
1H-NMR (CDCl3) δ: 4.64 (2H, d, J=5.8 Hz), 6.79 (1H, br s), 6.98-7.03 (4H, m), 7.10-7.14 (1H, m), 7.31-7.37 (4H, m), 7.39 (1H, d, J=8.0 Hz), 8.15 (1H, d, J=8.0 Hz).
A mixture of 0.30 g of N-(4-phenoxyphenyl)methyl-2,6-dichloronicotinic acid amide, 0.5 ml of 1,4-dioxane, and 2 ml of 28% aqueous ammonia was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 120° C. for 20 minutes. After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 120 mg of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide (hereinafter referred to as the present compound 61) and 63 mg of N-(4-phenoxyphenyl)methyl-6-amino-2-chloronicotinic acid amide.
The present compound 61
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.55-6.63 (3H, m), 6.98-7.02 (4H, m), 7.09-7.15 (1H, m), 7.29-7.36 (4H, m), 7.53 (1H, d, J=8.2 Hz).
1H-NMR (CDCl3) δ: 4.62 (2H, d, J=5.6 Hz), 4.86 (2H, br s), 6.47 (1H, d, J=8.5 Hz), 6.98-7.13 (6H, m), 7.30-7.37 (4H, m), 8.08 (1H, d, J=8.5 Hz).
0.13 g of 2-amino-6-methoxymethylnicotinic acid, 0.20 g of 4-phenoxybenzylamine, 0.27 g of triethylamine and 0.55 g of a BOP reagent were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 16 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with water, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.17 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 62).
The present compound 62
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.40 (2H, s), 4.57 (2H, d, J=5.8 Hz), 6.23-6.30 (1H, br m), 6.40 (2H, br s), 6.70 (1H, d, J=8.0 Hz), 6.98-7.02 (4H, m), 7.09-7.13 (1H, m), 7.29-7.36 (4H, m), 7.61 (1H, d, J=8.0 Hz).
0.30 g of N-(4-phenoxyphenyl)methyl-2-aminonicotinic acid amide and 0.18 g of N-bromosuccinimide were added to 10 ml of chlorofrom, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.16 g of N-(4-phenoxyphenyl)methyl-2-amino-5-bromonicotinic acid amide (hereinafter referred to as the present compound 63).
The present compound 63
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.38 (2H, br s), 6.98-7.03 (4H, m), 7.09-7.15 (1H, m), 7.28-7.38 (4H, m), 7.67 (1H, d, J=2.4 Hz), 8.18 (1H, d, J=2.4 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.16 g of ethyl iodide, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 86 mg of N-(4-ethoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 64).
The present compound 64
1H-NMR (CDCl3) δ: 1.42 (3H, t, J=7.0 Hz), 4.03 (2H, q, J=7.0 Hz), 4.53 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.86-6.90 (2H, m), 7.25-7.27 (2H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.14 g of bromobutane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel chromatography, so as to obtain 0.12 g of N-(4-butoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 65).
The present compound 65
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.3 Hz), 1.46-1.53 (2H, m), 1.73-1.80 (2H, m), 3.96 (2H, t, J=6.6 Hz), 4.52 (2H, d, J=5.6 Hz), 6.20 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.87-6.90 (2H, m), 7.24-7.27 (2H, m), 7.56 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.20 g of 1-iodopentane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel chromatography, so as to obtain 0.19 g of N-(4-pentyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 66).
The present compound 66
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.35-1.48 (4H, m), 1.76-1.82 (2H, m), 3.95 (2H, t, J=6.6 Hz), 4.52 (2H, d, J=5.4 Hz), 6.22 (1H, s), 6.36 (2H, s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.86-6.90 (2H, m), 7.23-7.27 (2H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.34 g of sodium 4-{[(2-aminopyridin-3-carbonyl)-amino]-methyl}-phenolate, 0.18 g of 1-bromoheptane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was successively washed with water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.18 g of N-(4-heptyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 67).
The present compound 67
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.8 Hz), 1.25-1.49 (8H, m), 1.74-1.82 (2H, m), 3.95 (2H, t, J=6.5 Hz), 4.52 (2H, d, J=5.4 Hz), 6.19 (1H, br s), 6.37 (2H, br s), 6.57 (1H, dd, J=7.8, 4.8 Hz), 6.86-6.89 (2H, m), 7.24-7.27 (2H, m), 7.57 (1H, dd, J=7.8, 1.8 Hz), 8.15 (1H, dd, J=4.8, 1.8 Hz).
14.8 g of triethylamine and 32.1 g of a BOP reagent were added to a mixture of 8.07 g of 2-aminonicotinic acid, 9.33 g of 4-hydroxybenzylamine hydrochloride and 100 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was wased with water, hexane and MTBE, so as to obtain 6.5 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide.
The present compound 68
1H-NMR (DMSO-D6) δ: 4.32 (2H, d, J=5.9 Hz), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.69-6.73 (2H, m), 7.06 (2H, br s), 7.09-7.14 (2H, m), 7.91 (1H, dd, J=7.7, 1.8 Hz), 8.06 (1H, dd, J=4.8, 1.8 Hz), 8.87 (1H, t, J=5.9 Hz), 9.29 (1H, s).
A mixture of 0.28 g of 2-aminonicotinic acid, 0.32 g of 1-hydroxybenzotriazole, 0.57 g of WSC, 0.23 g of 2-furylmethylamine and 2 ml of DMF was subjected to a microwave reactor (production name: MWO-1000; manufactured by EYELA) at 500 W at 60° C. for 5 minutes. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.33 g of N-(furan-2-yl)phenylmethyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 70).
The present compound 70
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.29-6.37 (5H, m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 7.39 (1H, dd, J=1.8, 0.8 Hz), 7.60 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 20 g of N-(4-phenoxyphenyl)methyl-2-chloro-6-methylnicotinic acid amide, 20 ml of 1,4-dioxane, 160 mg of copper(I) bromide and 100 ml of 28% aqueous ammonia was stirred at 180° C. for 9 hours. Thereafter, a saturated saline solution was added to the reaction mixture, and it was then extracted with chloroform four times. The organic layer was dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was successively washed with MTBE, a sodium hydroxide aqueous solution and water, and it was then dried, so as to obtain 13 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide.
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.19 g of 3-methoxypropane methane sulfonate, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 2 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was washed with a sodium hydroxide aqueous solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.20 g of N-[4-(3-methoxypropoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 71).
The present compound 71
1H-NMR (CDCl3) δ: 2.01-2.08 (2H, m), 3.35 (3H, s), 3.55 (2H, t, J=6.2 Hz), 4.05 (2H, t, J=6.2 Hz), 4.52 (2H, d, J=5.6 Hz), 6.33-6.38 (3H, m), 6.56 (1H, dd, J=7.6, 4.8 Hz), 6.87-6.89 (2H, m), 7.24-7.26 (2H, m), 7.58 (1H, dd, J=7.6, 1.7 Hz), 8.14 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.20 g of 1-bromo-5-methoxypentane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 2 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was washed with a sodium hydroxide aqueous solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.20 g of N-[4-(5-methoxypentyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 72).
The present compound 72
1H-NMR (CDCl3) δ: 1.50-1.68 (4H, m), 1.77-1.85 (2H, m), 3.34 (3H, s), 3.40 (2H, t, J=6.3 Hz), 3.96 (2H, t, J=6.6 Hz), 4.52 (2H, d, J=5.4 Hz), 6.20 (1H, s), 6.35 (2H, s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.86-6.89 (2H, m), 7.23-7.27 (2H, m), 7.57 (1H, dd, J=7.6, 1.8 Hz), 8.15 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.23 g of 6-methoxyhexane methane sulfonate, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 2 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.28 g of N-[4-(6-methoxyhexyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 73).
The present compound 73
1H-NMR (CDCl3) δ: 1.36-1.63 (6H, m), 1.75-1.82 (2H, m), 3.33 (3H, s), 3.38 (2H, t, J=6.6 Hz), 3.95 (2H, t, J=6.5 Hz), 4.52 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.86-6.90 (2H, m), 7.24-7.28 (2H, m), 7.56 (1H, dd, J=7.8, 1.6 Hz), 8.15 (1H, dd, J=4.9, 1.6 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.25 g of 7-methoxyheptane methane sulfonate, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 2 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.33 g of N-[4-(7-methoxyheptyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 74).
The present compound 74
1H-NMR (CDCl3) δ: 1.36-1.60 (8H, m), 1.74-1.82 (2H, m), 3.33 (3H, s), 3.37 (2H, t, J=6.6 Hz), 3.94 (2H, t, J=6.6 Hz), 4.52 (2H, d, J=5.4 Hz), 6.24 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.8, 4.9 Hz), 6.85-6.90 (2H, m), 7.23-7.28 (2H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.17 g of 1-bromo-2-ethoxyethane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 2 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.28 g of N-[4-(2-ethoxyethoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 75).
The present compound 75
1H-NMR (CDCl3) δ: 1.25 (3H, t, J=7.1 Hz), 3.60 (2H, q, J=7.1 Hz), 3.76-3.82 (2H, m), 4.10-4.14 (2H, m), 4.53 (2H, d, J=5.4 Hz), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.90-6.93 (2H, m), 7.24-7.27 (2H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.35 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.43 g of 4-ethoxybutan-p-toluene sulfonate, 0.60 g of cesium carbonate and 5 ml of DMF was stirred at 100° C. for 2 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.31 g of N-[4-(4-ethoxybutoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 76).
The present compound 76
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.0 Hz), 1.73-1.90 (4H, m), 3.46-3.51 (4H, m), 3.98 (2H, t, J=6.3 Hz), 4.53 (2H, d, J=5.6 Hz), 6.19 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.87-6.90 (2H, m), 7.24-7.27 (2H, m), 7.57 (1H, dd, J=7.7, 1.9 Hz), 8.15 (1H, dd, J=4.8, 1.9 Hz).
A mixture of 0.15 g of 2-amino-6-methylnicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.30 g of 4-benzyloxybenzylamine hydrochloride, 0.30 of WSC and 10 ml of pyridine was heated to reflux for 2 hours. Thereafter, 8 ml of DMF was added to the reaction mixture, and the obtained mixture was then heated to reflux for 2 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.23 g of N-(4-benzyloxyphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 77).
The present compound 77
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.52 (2H, d, J=5.3 Hz), 5.07 (2H, s), 6.17 (1H, br s), 6.39 (2H, br s), 6.43 (1H, d, J=8.0 Hz), 6.94-6.98 (2H, m), 7.24-7.28 (2H, m), 7.30-7.48 (6H, m).
0.30 g of N-(4-phenoxyphenyl)methyl-2-aminonicotinic acid amide and 0.14 g of N-chlorosuccinimide were added to 10 ml of chloroform. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.19 g of N-(4-phenoxyphenyl)methyl-2-amino-5-chloronicotinic acid amide (hereinafter referred to as the present compound 78).
The present compound 78
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.98-7.03 (4H, m), 7.09-7.15 (1H, m), 7.28-7.38 (4H, m), 7.56 (1H, d, J=2.4 Hz), 8.11 (1H, d, J=2.4 Hz).
A mixture of 0.27 g of 4-(3-methoxyphenoxy)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.25 g of N-[4-(3-methoxyphenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 79).
The present compound 79
1H-NMR (CDCl3) δ: 2.38 (3H, s), 3.78 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.24 (1H, br s), 6.38 (2H, br s), 6.44 (1H, d, J=7.7 Hz), 6.53-6.68 (3H, m), 7.00 (2H, d, J=8.7 Hz), 7.20-7.25 (1H, m), 7.28-7.32 (2H, m), 7.49 (1H, d, J=7.7 Hz).
A mixture of 0.27 g of 3-(4-methoxyphenoxy)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.31 g of N-[3-(4-methoxyphenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 80).
The present compound 80
1H-NMR (CDCl3) δ: 2.38 (3H, s), 3.80 (3H, s), 4.54 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.35 (2H, br s), 6.44 (1H, d, J=8.0 Hz), 6.82-7.02 (7H, m), 7.24-7.29 (1H, m), 7.47 (1H, d, J=8.0 Hz).
A mixture of 0.27 g of 4-(2-phenylethyl)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.16 g of N-[4-(2-phenylethyl)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 81).
The present compound 81
1H-NMR (CDCl3) δ: 2.38 (3H, s), 2.90-2.93 (4H, m), 4.56 (2H, d, J=5.6 Hz), 6.19 (1H, br s), 6.38 (2H, br s), 6.43 (1H, d, J=7.9 Hz), 7.16-7.31 (9H, m), 7.47 (1H, d, J=7.9 Hz).
A mixture of 0.29 g of 4-(4-fluorophenoxy)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.29 g of N-[4-(4-fluorophenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 82).
The present compound 82
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.39 (2H, br s), 6.44 (1H, d, J=7.8 Hz), 6.92-7.06 (6H, m), 7.25-7.31 (2H, m), 7.49 (1H, d, J=7.8 Hz).
A mixture of 0.28 g of 2-phenoxythiophen-5-ylmethylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.11 g of N-(2-phenoxythiophen-5-yl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 83).
The present compound 83
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.64 (2H, d, J=5.1 Hz), 6.25 (1H, br s), 6.35 (2H, br s), 6.39 (1H, d, J=3.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.74 (1H, d, J=3.9 Hz), 7.07-7.13 (3H, m), 7.30-7.36 (2H, m), 7.48 (1H, d, J=7.8 Hz).
A mixture of 0.27 g of 4-(benzyl)benzylamine hydrochloride, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried, so as to obtain 0.21 g of N-(4-benzylphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 84).
The present compound 84
1H-NMR (CDCl3) δ: 2.37 (3H, s), 3.97 (2H, s), 4.54 (2H, d, J=5.6 Hz), 6.20 (1H, br s), 6.38 (2H, br s), 6.42 (1H, d, J=7.7 Hz), 7.16-7.31 (9H, m), 7.46 (1H, d, J=7.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.11 g of 5-chloro-1-pentyne, 0.42 g of cesium carbonate, and 3 ml of DMF was stirred at 100° C. for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.26 g of N-[4-(4-pentynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 85).
The present compound 85
1H-NMR (CDCl3) δ: 1.97 (1H, t, J=2.7 Hz), 1.97-2.04 (2H, m), 2.41 (2H, td, J=7.0, 2.7 Hz), 4.07 (2H, t, J=6.0 Hz), 4.53 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.87-6.92 (2H, m), 7.24-7.28 (2H, m), 7.57 (1H, dd, J=7.7, 1.9 Hz), 8.15 (1H, dd, J=4.8, 1.9 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.13 g of 6-chloro-1-hexyne, 0.42 g of cesium carbonate, and 3 ml of DMF was stirred at 80° C. for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.29 g of N-[4-(5-hexynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 86).
The present compound 86
1H-NMR (CDCl3) δ: 1.69-1.76 (2H, m), 1.88-1.95 (2H, m), 1.97 (1H, t, J=2.5 Hz), 2.28 (2H, td, J=6.9, 2.6 Hz), 3.99 (2H, t, J=6.3 Hz), 4.53 (2H, d, J=5.3 Hz), 6.22 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.86-6.90 (2H, m), 7.24-7.28 (2H, m), 7.56-7.58 (1H, m), 8.15-8.17 (1H, m).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 2-chlorobenzyl chloride, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.28 g of N-[4-(2-chlorophenylmethoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 87).
The present compound 87
1H-NMR (CDCl3) δ: 4.53 (2H, d, J=5.3 Hz), 5.17 (2H, s), 6.26 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.96-6.99 (2H, m), 7.25-7.30 (4H, m), 7.39-7.42 (1H, m), 7.53-7.58 (2H, m), 8.15 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 3-chlorobenzyl chloride, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.34 g of N-[4-(3-chlorobenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 88).
The present compound 88
1H-NMR (CDCl3) δ: 4.53 (2H, d, J=5.6 Hz), 5.04 (2H, s), 6.24 (1H, br s), 6.37 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.93-6.96 (2H, m), 7.26-7.31 (5H, m), 7.43 (1H, s), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.15 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.17 g of 2-methoxybenzyl chloride, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.35 g of N-[4-(2-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 89).
The present compound 89
1H-NMR (CDCl3) δ: 3.87 (3H, s), 4.53 (2H, d, J=5.4 Hz), 5.12 (2H, s), 6.20 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.90-7.00 (4H, m), 7.25-7.32 (3H, m), 7.44 (1H, d, J=7.6 Hz), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.17 g of 3-methoxybenzyl chloride, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.35 g of N-[4-(3-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 90).
The present compound 90
1H-NMR (CDCl3) δ: 3.82 (3H, s), 4.53 (2H, d, J=5.6 Hz), 5.05 (2H, s), 6.21 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.86 (1H, dd, J=8.2, 2.3 Hz), 6.94-7.01 (4H, m), 7.25-7.32 (3H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.17 g of 4-methoxybenzyl chloride, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.34 g of N-[4-(4-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 91).
The present compound 91
1H-NMR (CDCl3) δ: 3.82 (3H, s), 4.53 (2H, d, J=5.4 Hz), 4.99 (2H, s), 6.37 (3H, br s), 6.57 (1H, dd, J=8.0, 4.9 Hz), 6.90-6.96 (4H, m), 7.25-7.27 (2H, m), 7.33-7.36 (2H, m), 7.59 (1H, dd, J=8.0, 1.6 Hz), 8.15 (1H, dd, J=4.9, 1.6 Hz).
A mixture of 0.28 g of 3-phenoxybenzylamine hydrochloride, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium bicarbonate aqueous solution, water, MTBE and hexane, and it was then dried under reduced pressure, so as to obtain 0.20 g of N-(3-phenoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 92).
The present compound 92
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.56 (2H, d, J=5.8 Hz), 6.24 (1H, br s), 6.35 (2H, br s), 6.44 (1H, d, J=7.8 Hz), 6.89-7.14 (6H, m), 7.29-7.36 (3H, m), 7.47 (1H, d, J=7.8 Hz).
A mixture of 0.18 g of N-(2-fluorophenyl)methyl-2-amino-6-chloronicotinic acid amide, 0.27 g of tributyl(methoxymethyl) tin, 2 ml of N-methylpyrrolidone and 0.05 g of bistriphenylphosphine palladium dichloride was stirred at 130° C. for 3 hours. Thereafter, ethyl acetate and diluted hydrochloric acid were added to the reaction mixture, and the obtained mixture was then stirred, so as to separate a water layer. Thereafter, sodium hydroxide was added to the water layer to adjust the pH value to pH 4, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.06 g of N-(2-fluorophenyl)methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 93).
The present compound 93
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.65 (2H, d, J=5.6 Hz), 6.32-6.43 (3H, br m), 6.70 (1H, d, J=7.9 Hz), 7.05-7.16 (2H, m), 7.25-7.33 (1H, m), 7.37-7.43 (1H, m), 7.61 (1H, d, J=7.9 Hz).
A mixture of 0.18 g of 2-fluoro-3-methoxybenzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.23 g of N-(2-fluoro-3-methoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 94).
The present compound 94
1H-NMR (CDCl3) δ: 2.38 (3H, s), 3.89 (3H, s), 4.64 (2H, dd, J=5.8, 1.0 Hz), 6.32-6.39 (3H, br m), 6.44 (1H, d, J=7.7 Hz), 6.89-6.98 (2H, m), 7.03-7.08 (1H, m), 7.49 (1H, d, J=7.7 Hz).
A mixture of 0.17 g of 3-methoxybenzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.22 g of N-(3-methoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 95).
The present compound 95
1H-NMR (CDCl3) δ: 2.38 (3H, s), 3.81 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.39 (2H, br s), 6.44 (1H, d, J=8.0 Hz), 6.82-6.94 (3H, m), 7.24-7.30 (1H, m), 7.49 (1H, d, J=8.0 Hz).
A mixture of 0.25 g of 4-(4-methylphenoxy)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.34 g of N-[4-(4-methylphenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 96).
The present compound 96
1H-NMR (CDCl3) δ: 2.34 (3H, s), 2.38 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.38 (2H, br s), 6.44 (1H, d, J=8.0 Hz), 6.89-6.98 (4H, m), 7.12-7.16 (2H, m), 7.26-7.32 (2H, m), 7.48 (1H, d, J=8.0 Hz).
A mixture of 0.25 g of 3-(3-methylphenoxy)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.27 g of N-[3-(3-methylphenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 97).
The present compound 97
1H-NMR (CDCl3) δ: 2.33 (3H, s), 2.38 (3H, s), 4.56 (2H, d, J=5.8 Hz), 6.25 (1H, br s), 6.37 (2H, br s), 6.44 (1H, d, J=7.8 Hz), 6.79-6.84 (2H, m), 6.89-6.99 (3H, m), 7.03-7.08 (1H, m), 7.19-7.24 (1H, m), 7.27-7.32 (1H, m), 7.48 (1H, d, J=7.8 Hz).
A mixture of 0.21 g of 3-pentylbenzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.22 g of N-(3-pentylphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 98).
The present compound 98
1H-NMR (CDCl3) δ: 0.86-0.91 (3H, m), 1.28-1.36 (4H, m), 1.57-1.66 (2H, m), 2.38 (3H, s), 2.57-2.63 (2H, m), 4.56 (2H, d, J=5.6 Hz), 6.21 (1H, br s), 6.39 (2H, br s), 6.43 (1H, d, J=7.8 Hz), 7.10-7.16 (3H, m), 7.25-7.29 (1H, m), 7.48 (1H, d, J=7.8 Hz).
A mixture of 0.21 g of 4-pentylbenzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.32 g of N-(4-pentylphenyl)methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 99).
The present compound 99
1H-NMR (CDCl3) δ: 0.87-0.91 (3H, m), 1.29-1.36 (4H, m), 1.57-1.64 (2H, m), 2.38 (3H, s), 2.57-2.62 (2H, m), 4.55 (2H, d, J=5.3 Hz), 6.19 (1H, br s), 6.38 (2H, br s), 6.43 (1H, d, J=7.7 Hz), 7.17 (2H, d, J=8.0 Hz), 7.23-7.27 (2H, m), 7.47 (1H, d, J=7.7 Hz).
A mixture of 0.25 g of 4-(phenoxymethyl)benzylamine, 0.15 g of 2-amino-6-methylnicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.32 g of N-[4-(phenoxymethyl)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 100).
The present compound 100
1H-NMR (CDCl3) δ: 2.38 (3H, s), 4.59 (2H, d, J=5.6 Hz), 5.06 (2H, s), 6.27 (1H, br s), 6.40 (2H, br s), 6.43 (1H, d, J=7.8 Hz), 6.94-7.00 (3H, m), 7.24-7.51 (7H, m).
0.28 g of 2-amino-6-chloronicotinic acid, 0.27 g of 2-fluorobenzylamine, 0.30 g of triethylamine and 0.90 g of a BOP reagent were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 48 hours. After water was added to the reaction mixture, the mixture was extracted ethyl acetate. The organic layer was washed with water. The resultant was dried over sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was washed with hexane, so as to obtain 0.38 g of N-(2-fluorophenyl)methyl-2-amino-6-chloronicotinic acid amide (hereinafter referred to as the present compound 101).
The present compound 101
1H-NMR (CDCl3) δ: 4.63 (2H, d, J=5.9 Hz), 6.34 (1H, br s), 6.56 (2H, br s), 6.58 (1H, d, J=8.0 Hz), 7.05-7.16 (2H, m), 7.26-7.33 (1H, m), 7.36-7.41 (1H, m), 7.52 (1H, d, J=8.0 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 81 mg of 3-bromo-1-propyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at 60° C. for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.22 g of N-[4-(2-propynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 102).
The present compound 102
1H-NMR (CDCl3) δ: 2.52-2.53 (1H, m), 4.54 (2H, d, J=5.6 Hz), 4.69-4.70 (2H, m), 6.24 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.95-7.00 (2H, m), 7.26-7.30 (2H, m), 7.57 (1H, d, J=7.6 Hz), 8.16 (1H, d, J=4.9 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.08 g of 3-bromo-1-propene, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 6 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was washed with a sodium hydroxide aqueous solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.14 g of N-[4-(2-propenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 103).
The present compound 103
1H-NMR (CDCl3) δ: 4.52-4.56 (4H, m), 5.30 (1H, d, J=10.7 Hz), 5.42 (1H, d, J=17.3 Hz), 6.02-6.10 (1H, m), 6.21 (1H, br s), 6.36 (2H, br s), 6.56-6.60 (1H, m), 6.90-6.93 (2H, m), 7.25-7.29 (2H, m), 7.57 (1H, d, J=7.8 Hz), 8.16 (1H, d, J=4.9 Hz).
A mixture of 0.21 g of 2-aminonicotinic acid, 0.23 g of 1-hydroxybenzotriazole, 0.37 g of WSC, 0.19 g of 3-fluorobenzylamine and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.26 g of N-(3-fluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 104).
The present compound 104
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.34-6.43 (3H, m), 6.57-6.61 (1H, m), 6.96-7.13 (3H, m), 7.29-7.35 (1H, m), 7.62 (1H, d, J=7.6 Hz), 8.16-8.18 (1H, m).
A mixture of 0.21 g of 2-aminonicotinic acid, 0.23 g of 1-hydroxybenzotriazole, 0.37 g of WSC, 0.18 g of 3-methylbenzylamine and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water, and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.19 g of N-(3-methylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 105).
The present compound 105
1H-NMR (CDCl3) δ: 2.36 (3H, s), 4.57 (2H, d, J=5.4 Hz), 6.26 (1H, br s), 6.37 (2H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 7.12-7.16 (3H, m), 7.24-7.27 (1H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.21 g of 2-aminonicotinic acid, 0.23 g of 1-hydroxybenzotriazole, 0.37 g of WSC, 0.18 g of 4-methylbenzylamine and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.43 g of N-(4-methylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 106).
The present compound 106
1H-NMR (CDCl3) δ: 2.35 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.35 (2H, br s), 6.55-6.59 (1H, m), 7.16-7.26 (4H, m), 7.57 (1H, d, J=7.6 Hz), 8.15-8.17 (1H, m).
0.82 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.21 g of 2-aminonicotinic acid, 0.20 g of 4-ethylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.34 g of N-(4-ethylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 107).
The present compound 107
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.6 Hz), 2.65 (2H, q, J=7.6 Hz), 4.57 (2H, d, J=5.3 Hz), 6.23 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 7.19-7.22 (2H, m), 7.25-7.29 (2H, m), 7.57 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
0.55 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.12 g of 2-methylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.21 g of N-(2-methylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 108).
The present compound 108
1H-NMR (CDCl3) δ: 2.37 (3H, s), 4.60 (2H, d, J=5.1 Hz), 6.12 (1H, br s), 6.37 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 7.19-7.31 (4H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
0.55 g of a BOP reagent and 0.25 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.20 g of 4-butylbenzylamine hydrochloride and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.26 g of N-(4-butylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 109).
The present compound 109
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.3 Hz), 1.32-1.39 (2H, m), 1.54-1.63 (2H, m), 2.61 (2H, t, J=7.7 Hz), 4.56 (2H, d, J=5.4 Hz), 6.24 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 7.17-7.19 (2H, m), 7.24-7.27 (2H, m), 7.58 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.82 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.21 g of 2-aminonicotinic acid, 0.29 g of 4-hexylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.40 g of N-(4-hexylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 110).
The present compound 110
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.9 Hz), 1.27-1.35 (6H, m), 1.56-1.62 (2H, m), 2.60 (2H, t, J=7.7 Hz), 4.56 (2H, d, J=5.6 Hz), 6.24 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 7.16-7.20 (2H, m), 7.24-7.28 (2H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
0.55 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.23 g of 4-heptylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.28 g of N-(4-heptylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound III).
The present compound 111
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.8 Hz), 1.26-1.34 (8H, m), 1.58-1.62 (2H, m), 2.60 (2H, t, J=7.7 Hz), 4.56 (2H, d, J=5.4 Hz), 6.23 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 7.16-7.19 (2H, m), 7.24-7.27 (2H, m), 7.58 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.55 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.22 g of 3-fluoro-4-phenoxybenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.28 g of N-(3-fluoro-4-phenoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 112).
The present compound 112
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.9 Hz), 6.39 (3H, br s), 6.59-6.62 (1H, m), 6.96-7.20 (6H, m), 7.30-7.35 (2H, m), 7.63 (1H, dd, J=7.7, 1.6 Hz), 8.16-8.19 (1H, m).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.21 g of 3,5-difluorobenzyl bromide, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.16 g of N-[4-(3,5-difluorobenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 113).
The present compound 113
1H-NMR (CDCl3) δ: 4.54 (2H, d, J=5.6 Hz), 5.05 (2H, s), 6.23 (1H, br s), 6.37 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.73-6.78 (1H, m), 6.92-6.97 (4H, m), 7.26-7.29 (2H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.23 g of 2-fluoro-3-methoxyphenylmethyl methanesulfonate, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at 100° C. for 3 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water, and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.29 g of N-[4-(2-fluoro-3-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 114).
The present compound 114
1H-NMR (CDCl3) δ: 3.90 (3H, s), 4.53 (2H, d, J=5.4 Hz), 5.14 (2H, s), 6.22 (1H, br s), 6.36 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.92-7.00 (3H, m), 7.05-7.10 (2H, m), 7.26-7.28 (2H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 312 mg of 4-(3-chloro-4-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 200 mg of N-[4-(3-chloro-4-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 115).
The present compound 115
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.32-6.41 (3H, br m), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.86-6.91 (1H, m), 6.95-6.99 (2H, m), 7.01-7.06 (1H, m), 7.08-7.13 (1H, m), 7.31-7.34 (2H, m), 7.61 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
1.0 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide and 0.91 g of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetan-2,4-disulfide (a Lawesson's reagent) were added to 10 ml of 1,4-dioxane. The obtained mixture was heated to reflux for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 197 mg of N-(4-phenoxyphenyl)methyl-2-amino-6-methyl-nicotinic acid thioamide (hereinafter referred to as the present compound 116).
The present compound 116
1H-NMR (CDCl3) δ: 2.36 (3H, s), 4.91 (2H, d, J=5.1 Hz), 5.95 (2H, br s), 6.48 (1H, d, J=7.7 Hz), 6.99-7.04 (4H, m), 7.13 (1H, td, J=7.4, 1.0 Hz), 7.31-7.38 (5H, m), 7.66 (1H, br s).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 332 mg of 4-(4-chloro-4-ethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 244 mg of N-[4-(4-chloro-4-ethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 117).
The present compound 117
1H-NMR (CDCl3) δ: 1.21 (3H, t, J=7.5 Hz), 2.72 (2H, q, J=7.5 Hz), 4.58 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.8, 4.8 Hz), 6.76 (1H, dd, J=8.7, 2.9 Hz), 6.91 (1H, d, J=2.9 Hz), 6.96-6.99 (2H, m), 7.28 (1H, d, J=8.7 Hz), 7.31 (2H, d, J=8.8 Hz), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 292 mg of 4-(2,4-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 266 mg of N-[4-(2,4-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 118).
The present compound 118
1H-NMR (CDCl3) δ: 2.17 (3H, s), 2.32 (3H, s), 4.53 (2H, d, J=5.6 Hz), 6.33-6.43 (1H, br m), 6.48 (2H, br s), 6.56 (1H, dd, J=7.6, 4.9 Hz), 6.81 (1H, d, J=8.1 Hz), 6.82-6.87 (2H, m), 6.95-7.00 (1H, m), 7.06 (1H, s), 7.24 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.6, 1.8 Hz), 8.12 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 237 mg of 4-(3,4-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 214 mg of N-[4-(3,4-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 119).
The present compound 119
1H-NMR (CDCl3) δ: 2.24 (6H, s), 4.56 (2H, d, J=5.6 Hz), 6.32 (1H, br s), 6.41 (2H, br s), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.75 (1H, dd, J=8.2, 2.4 Hz), 6.82 (1H, d, J=2.4 Hz), 6.94-6.97 (2H, m), 7.09 (1H, d, J=8.2 Hz), 7.28 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 311 mg of 4-(2,4,6-trimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 246 mg of N-[4-(2,4,6-trimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 120).
The present compound 120
1H-NMR (CDCl3) δ: 2.07 (6H, s), 2.30 (3H, s), 4.52 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.39 (2H, br s), 6.57 (1H, dd, J=7.8, 4.8 Hz), 6.72-6.76 (2H, m), 6.90 (2H, s), 7.21 (2H, d, J=8.8 Hz), 7.58 (1H, dd, J=7.8, 1.8 Hz), 8.14 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 316 mg of 4-(2,3,6-trimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 242 mg of N-[4-(2,3,6-trimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 121).
The present compound 121
1H-NMR (CDCl3) δ: 2.03 (3H, s), 2.08 (3H, s), 2.27 (3H, s), 4.52 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.42 (2H, br s), 6.57 (1H, dd, J=7.7, 4.9 Hz), 6.71-6.75 (2H, m), 6.96 (1H, d, J=7.8 Hz), 6.99 (1H, d, J=7.8 Hz), 7.22 (2H, d, J=8.8 Hz), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.14 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 328 mg of 4-(3-ethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 171 mg of N-[4-(3-ethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 122).
The present compound 122
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.7 Hz), 2.63 (2H, q, J=7.7 Hz), 4.57 (2H, d, J=5.6 Hz), 6.37 (3H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.81 (1H, dd, J=8.0, 1.9 Hz), 6.86-6.88 (1H, m), 6.94-7.01 (3H, m), 7.23 (1H, d, J=8.0 Hz), 7.29 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.7, 1.7 Hz), 8.15 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 296 mg of 4-[3-(1-methylethyl)phenoxy]benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 194 mg of N-{4-[3-(1-methylethyl)phenoxy]phenyl}methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 123).
The present compound 123
1H-NMR (CDCl3) δ: 1.24 (6H, d, J=7.0 Hz), 2.83-2.94 (1H, m), 4.57 (2H, d, J=5.6 Hz), 6.31-6.44 (3H, br m), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.79 (1H, ddd, J=8.0, 2.2, 1.0 Hz), 6.90-6.92 (1H, m), 6.97-7.01 (3H, m), 7.24 (1H, d, J=8.0 Hz), 7.30 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 302 mg of 4-(4-propylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 125 mg of N-[4-(4-propylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 124).
The present compound 124
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.3 Hz), 1.58-1.69 (2H, m), 2.57 (2H, t, J=7.6 Hz), 4.56 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.91-6.94 (2H, m), 6.95-6.99 (2H, m), 7.14 (2H, d, J=8.6 Hz), 7.29 (2H, d, J=8.6 Hz), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 330 mg of 4-(4-butylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 173 mg of N-[4-(4-butylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 125).
The present compound 125
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.3 Hz), 1.31-1.41 (2H, m), 1.55-1.63 (2H, m), 2.59 (2H, t, J=7.7 Hz), 4.56 (2H, d, J=5.6 Hz), 6.24 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 5.0 Hz), 6.90-6.94 (2H, m), 6.95-6.99 (2H, m), 7.14 (2H, d, J=8.7 Hz), 7.29 (2H, d, J=8.7 Hz), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=5.0, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 247 mg of 4-(2-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 51 mg of N-[4-(2-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 126).
The present compound 126
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.48 (2H, br s), 6.59 (1H, dd, J=7.7, 5.0 Hz), 6.92-6.96 (2H, m), 7.01 (1H, dd, J=8.0, 1.5 Hz), 7.11 (1H, td, J=7.7, 1.5 Hz), 7.21-7.27 (1H, m), 7.31 (2H, d, J=8.8 Hz), 7.47 (1H, dd, J=8.0, 1.6 Hz), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=5.0, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 296 mg of 4-(3,5-dichlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 112 mg of N-[4-(3,5-dichlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 127).
The present compound 127
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.8 Hz), 6.33-6.42 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.86 (2H, d, J=1.8 Hz), 7.00-7.04 (2H, m), 7.08 (1H, t, J=1.8 Hz), 7.34-7.38 (2H, m), 7.62 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 316 mg of 4-(3,4-dichlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 88 mg of N-[4-(3,4-dichlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 128).
The present compound 128
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.30-6.43 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.86 (1H, dd, J=8.7, 2.8 Hz), 6.98-7.02 (2H, m), 7.07 (1H, d, J=2.8 Hz), 7.35 (2H, d, J=8.6 Hz), 7.38 (1H, d, J=8.7 Hz), 7.61 (1H, dd, J=7.7, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 293 mg of 4-(2-chloro-4,5-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 139 mg of N-[4-(2-chloro-4,5-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 129).
The present compound 129
1H-NMR (CDCl3) δ: 2.19 (3H, s), 2.23 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.31-6.39 (3H, br m), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.82 (1H, s), 6.87-6.90 (2H, m), 7.21 (1H, s), 7.27 (2H, d, J=8.6 Hz), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.14 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.28 g of 2-aminonicotinic acid, 0.32 g of 1-hydroxybenzotriazole, 0.57 g of WSC, 0.27 g of 2-thienylmethylamine and 2 ml of DMF was subjected to a microwave reactor (production name: MWO-1000; manufactured by EYELA) at 500 W at 60° C. for 5 minutes. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.34 g of N-[(thiophen-2-yl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 130).
The present compound 130
1H-NMR (CDCl3) δ: 4.78 (2H, d, J=5.6 Hz), 6.29-6.39 (3H, br m), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.98 (1H, dd, J=5.1, 3.5 Hz), 7.03-7.05 (1H, m), 7.25-7.28 (1H, m), 7.58 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 1.0 g of N-(4-phenoxyphenyl)methyl-2-chloro-6-methylnicotinic acid amide, 1.9 g of sodium azide and 15 ml of DMF was heated to reflux for 2 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.76 g of N-(4-phenoxyphenyl)methyl-2-azide-6-methylnicotinic acid amide. N-(4-phenoxyphenyl)methyl-2-azide-6-methylnicotinic acid amide
1H-NMR (CDCl3) δ: 3.03 (3H, d, J=0.7 Hz), 4.76 (2H, d, J=5.8 Hz), 6.97-7.03 (4H, m), 7.07-7.12 (1H, m), 7.18-7.21 (1H, m), 7.30-7.41 (4H, m), 8.56 (1H, d, J=7.2 Hz), 9.37 (1H, br s).
A mixture of 0.76 g of N-(4-phenoxyphenyl)methyl-2-azide-6-methylnicotinic acid amide, 1.5 g of tin chloride dehydrate, 5 ml of methanol and 5 ml of 10N hydrochloric acid was heated to reflux for 1 hour. Thereafter, a sodium hydroxide aqueous solution was added to the reaction mixture, and it was then extracted with chloroform three times. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.50 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide.
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 361 mg of 4-(4-trifluoromethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 253 mg of N-[4-(4-trifluoromethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 131).
The present compound 131
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.98-7.02 (4H, m), 7.18 (2H, d, J=8.3 Hz), 7.33 (2H, d, J=8.8 Hz), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 285 mg of 4-(2,5-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 102 mg of N-[4-(2,5-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 132).
The present compound 132
1H-NMR (CDCl3) δ: 2.17 (3H, s), 2.28 (3H, s), 4.55 (2H, d, J=5.3 Hz), 6.23 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.73 (1H, s), 6.85-6.92 (3H, m), 7.13 (1H, d, J=7.6
Hz), 7.25-7.29 (2H, m), 7.58 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 342 mg of 4-(4-trifluoromethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 234 mg of N-[4-(4-trifluoromethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 133).
The present compound 133
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.6 Hz), 6.37 (3H, br s), 6.59 (1H, dd, J=7.6, 4.8 Hz), 7.02-7.06 (4H, m), 7.36 (2H, d, J=8.6 Hz), 7.57 (2H, d, J=8.3 Hz), 7.61 (1H, dd, J=7.6, 1.7 Hz), 8.17 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.30 g of 3-(4-methylphenoxy)benzylamine, 0.20 g of 2-aminonicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.42 g of N-[3-(4-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 134).
The present compound 134
1H-NMR (CDCl3) δ: 2.34 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.34 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.88-6.96 (4H, m), 7.03 (1H, d, J=7.6 Hz), 7.14 (2H, d, J=8.0 Hz), 7.29 (1H, dd, J=7.6, 8.0 Hz), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.40 g of 4-(3-methylphenoxy)benzylamine, 0.20 g of 2-aminonicotinic acid, 0.15 g of 1-hydroxybenzotriazole, 0.25 g of WSC, 0.35 g of pyridine and 2 ml of DMF was stirred under heating to reflux for 30 minutes, and then at a room temperature for 1 day. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.44 g of N-[4-(3-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 135).
The present compound 135
1H-NMR (CDCl3) δ: 2.33 (3H, s), 4.57 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.79-6.84 (2H, m), 6.91-6.95 (1H, m), 6.96-7.02 (2H, m), 7.19-7.24 (1H, m), 7.30 (2H, d, J=8.5 Hz), 7.60 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
0.51 g of a BOP reagent and 0.25 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.17 g of 3-ethylbenzylamine hydrochloride and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.22 g of N-(3-ethylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 136).
The present compound 136
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.7 Hz), 2.66 (2H, q, J=7.6 Hz), 4.58 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 7.13-7.18 (3H, m), 7.27-7.30 (1H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
0.51 g of a BOP reagent and 0.12 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.15 g of 3-propylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.21 g of N-(3-propylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 137).
The present compound 137
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.4 Hz), 1.60-1.69 (2H, m), 2.59 (2H, t, J=7.7 Hz), 4.58 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 7.12-7.17 (3H, m), 7.26-7.30 (1H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
0.51 g of a BOP reagent and 0.25 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.16 g of 3-butylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water, and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.13 g of N-(3-butylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 138).
The present compound 138
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.4 Hz), 1.34-1.39 (2H, m), 1.57-1.67 (2H, m), 2.61 (2H, t, J=7.7 Hz), 4.58 (2H, d, J=5.3 Hz), 6.24 (1H, br s), 6.39 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 7.10-7.16 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.2 Hz), 8.16 (1H, dd, J=4.8, 1.2 Hz).
0.51 g of a BOP reagent and 0.25 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.19 g of 3-hexylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.17 g of N-(3-hexylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 139).
The present compound 139
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=7.0 Hz), 1.23-1.34 (6H, m), 1.55-1.64 (2H, m), 2.60 (2H, t, J=7.7 Hz), 4.57 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.50 (2H, br s), 6.59 (1H, dd, J=7.8, 4.9 Hz), 7.12-7.16 (3H, m), 7.25-7.29 (1H, m), 7.60 (1H, dd, J=7.8, 1.6 Hz), 8.14 (1H, dd, J=4.9, 1.6 Hz).
0.51 g of a BOP reagent was added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.20 g of 3-isobutylbenzylamine hydrochloride, 0.25 g of triethylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.26 g of N-(3-isobutylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 140).
The present compound 140
1H-NMR (CDCl3) δ: 0.90 (6H, d, J=6.8 Hz), 1.82-1.90 (1H, m), 2.47 (2H, d, J=7.2 Hz), 4.57 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 7.08-7.16 (3H, m), 7.25-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.4 Hz), 8.16 (1H, dd, J=4.8, 1.4 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.15 g of 2-fluorophenylmethyl chloride, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.27 g of N-[3-(2-fluorobenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 141).
The present compound 141
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.4 Hz), 5.13 (2H, s), 6.29 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.91-6.98 (3H, m), 7.05-7.18 (2H, m), 7.26-7.32 (2H, m), 7.46-7.51 (1H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.19 g of 3-fluorophenylmethyl bromide, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.11 g of N-[3-(3-fluorobenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 142).
The present compound 142
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 5.06 (2H, s), 6.28 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.88-7.02 (4H, m), 7.12-7.19 (2H, m), 7.27-7.36 (2H, m), 7.57 (1H, dd, J=7.6, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.20 g of 4-fluorophenylmethyl methanesulfonate, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.21 g of N-[3-(4-fluorobenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 143).
The present compound 143
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 5.03 (2H, s), 6.26 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.88-6.95 (3H, m), 7.03-7.08 (2H, m), 7.26-7.30 (1H, m), 7.37-7.42 (2H, m), 7.55-7.58 (1H, m), 8.17 (1H, dd, J=4.9, 1.5 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.19 g of 2-methylphenylmethyl bromide, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.24 g of N-[3-(2-methylbenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 144).
The present compound 144
1H-NMR (CDCl3) δ: 2.37 (3H, s), 4.58 (2H, d, J=5.6 Hz), 5.04 (2H, s), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.92-6.98 (3H, m), 7.19-7.31 (4H, m), 7.39 (1H, d, J=7.3 Hz), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.14 g of 3-methylphenylmethyl chloride, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.24 g of N-[3-(3-methylbenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 145).
The present compound 145
1H-NMR (CDCl3) δ: 2.36 (3H, s), 4.57 (2H, d, J=5.6 Hz), 5.02 (2H, s), 6.29 (1H, br s), 6.35-6.38 (2H, br m), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.90-6.96 (3H, m), 7.12-7.15 (1H, m), 7.20-7.29 (4H, m), 7.56 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.16 g of 2-methoxyphenylmethyl chloride, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.30 g of N-[3-(2-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 146).
The present compound 146
1H-NMR (CDCl3) δ: 3.85 (3H, s), 4.56 (2H, d, J=5.6 Hz), 5.11 (2H, s), 6.29 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.6, 4.9 Hz), 6.89-6.98 (5H, m), 7.25-7.31 (2H, m), 7.43 (1H, d, J=7.1 Hz), 7.56 (1H, d, J=7.6 Hz), 8.15 (1H, d, J=3.4 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.16 g of 3-methoxyphenylmethyl chloride, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.25 g of N-[3-(3-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 147).
The present compound 147
1H-NMR (CDCl3) δ: 3.81 (3H, s), 4.57 (2H, d, J=5.6 Hz), 5.05 (2H, s), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.85 (1H, dd, J=8.2, 2.1 Hz), 6.90-7.00 (5H, m), 7.25-7.30 (2H, m), 7.56 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.16 g of 4-methoxybenzyl chloride, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.30 g of N-[3-(4-methoxybenzyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 148).
The present compound 148
1H-NMR (CDCl3) δ: 3.81 (3H, s), 4.57 (2H, d, J=5.6 Hz), 4.99 (2H, s), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.87-6.95 (5H, m), 7.25-7.29 (1H, m), 7.32-7.36 (2H, m), 7.57 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 333 mg of 4-(4-ethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 243 mg of N-[4-(4-ethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 149).
The present compound 149
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.6 Hz), 2.64 (2H, q, J=7.6 Hz), 4.56 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.91-6.99 (4H, m), 7.17 (2H, d, J=8.6 Hz), 7.29 (2H, d, J=8.6 Hz), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.35 g of 4-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.10 g of N-[4-(5,6,7,8-tetrahydronaphthalen-2-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 150).
The present compound 150
1H-NMR (CDCl3) δ: 1.76-1.82 (4H, m), 2.70-2.76 (4H, m), 4.56 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.71-6.77 (2H, m), 6.97 (2H, d, J=8.7 Hz), 7.03 (1H, d, J=8.1 Hz), 7.28 (2H, d, J=8.7 Hz), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.33 g of 4-(3-methylphenylthio)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[4-(3-methylphenylthio)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 151).
The present compound 151
1H-NMR (CDCl3) δ: 2.32 (3H, s), 4.58 (2H, d, J=5.6 Hz), 6.26-6.41 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 7.06-7.10 (1H, m), 7.13-7.17 (1H, m), 7.18-7.22 (2H, m), 7.22-7.32 (4H, m), 7.59 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.30 g of 4-(3-methoxyphenylthio)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.16 g of N-[4-(3-methoxyphenylthio)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 152).
The present compound 152
1H-NMR (CDCl3) δ: 3.77 (3H, s), 4.58 (2H, d, J=5.8 Hz), 6.28-6.40 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.79 (1H, ddd, J=8.3, 2.5, 0.8 Hz), 6.87-6.88 (1H, m), 6.90-6.93 (1H, m), 7.20-7.24 (1H, m), 7.25-7.30 (2H, m), 7.31-7.36 (2H, m), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.38 g of 4-(4-methoxyphenylthio)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.14 g of N-[4-(4-methoxyphenylthio)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 153).
The present compound 153
1H-NMR (CDCl3) δ: 3.83 (3H, s), 4.53 (2H, d, J=5.6 Hz), 6.24 (1H, br s), 6.34 (2H, br s), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.88-6.92 (2H, m), 7.14 (2H, d, J=8.6 Hz), 7.21 (2H, d, J=8.6 Hz), 7.40-7.43 (2H, m), 7.57 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 324 mg of 4-(4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 146 mg of N-[4-(4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 154).
The present compound 154
1H-NMR (CDCl3) δ: 2.48 (3H, s), 4.57 (2H, d, J=5.6 Hz), 6.31 (1H, br s), 6.38 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.93-7.00 (4H, m), 7.25-7.32 (4H, m), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 369 mg of 4-(2-methyl-4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 171 mg of N-[4-(2-methyl-4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 155).
The present compound 155
1H-NMR (CDCl3) δ: 2.20 (3H, s), 2.48 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.37 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.83-6.89 (3H, m), 7.09 (1H, dd, J=8.2, 2.1 Hz), 7.18 (1H, d, J=1.8 Hz), 7.25-7.29 (2H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8
Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 342 mg of 4-(2,3-dimethyl-4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 109 mg of N-[4-(2,3-dimethyl-4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 156).
The present compound 156
1H-NMR (CDCl3) δ: 2.16 (3H, s), 2.36 (3H, s), 2.44 (3H, s), 4.54 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.80 (1H, d, J=8.6 Hz), 6.85 (2H, d, J=8.6 Hz), 7.08 (1H, d, J=8.6 Hz), 7.26 (2H, d, J=8.6 Hz), 7.58 (1H, dd, J=7.8, 1.6 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 349 mg of 4-(4-chloro-3,5-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 286 mg of N-[4-(4-chloro-3,5-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 157).
The present compound 157
1H-NMR (CDCl3) δ: 2.34 (6H, s), 4.57 (2H, d, J=5.6 Hz), 6.32-6.42 (3H, br m), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.74 (2H, s), 6.96 (2H, d, J=8.7 Hz), 7.30 (2H, d, J=8.7 Hz), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 391 mg of 4-(3-ethyl-4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 200 mg of N-[4-(3-ethyl-4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 158).
The present compound 158
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.5 Hz), 2.45 (3H, s), 2.73 (2H, q, J=7.5 Hz), 4.57 (2H, d, J=5.6 Hz), 6.28-6.41 (3H, br m), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.83 (1H, dd, J=8.6, 2.8 Hz), 6.89 (1H, d, J=2.5 Hz), 6.97 (2H, d, J=8.6 Hz), 7.20 (1H, d, J=8.6 Hz), 7.30 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 339 mg of 3-(4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 124 mg of N-[3-(4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 159).
The present compound 159
1H-NMR (CDCl3) δ: 2.48 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.32-6.42 (3H, br m), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.90 (1H, dd, J=7.8, 2.0 Hz), 6.94-6.97 (3H, m), 7.06 (1H, d, J=7.6 Hz), 7.24-7.33 (3H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 349 mg of 4-(3-chloro-4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 179 mg of N-[4-(3-chloro-4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 160).
The present compound 160
1H-NMR (CDCl3) δ: 2.47 (3H, s), 4.59 (2H, d, J=5.6 Hz), 6.28-6.42 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.93 (1H, dd, J=8.7, 2.6 Hz), 6.99 (2H, d, J=8.7 Hz), 7.04 (1H, d, J=2.6 Hz), 7.18 (1H, d, J=8.7 Hz), 7.33 (2H, d, J=8.7 Hz), 7.61 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 404 mg of 4-(3-chloro-4-ethylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 278 mg of N-[4-(3-chloro-4-ethylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 161).
The present compound 161
1H-NMR (CDCl3) δ: 1.32 (3H, t, J=7.3 Hz), 2.93 (2H, q, J=7.3 Hz), 4.58 (2H, d, J=5.8 Hz), 6.34-6.41 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.88 (1H, dd, J=8.6, 2.7 Hz), 7.00 (2H, d, J=8.6 Hz), 7.04 (1H, d, J=2.7 Hz), 7.30 (1H, d, J=8.6 Hz), 7.33 (2H, d, J=8.6 Hz), 7.62 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 409 mg of 4-(3-methoxy-4-methylthiophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, and followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 260 mg of N-[4-(3-methoxy-4-methylthiophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 162).
The present compound 162
1H-NMR (CDCl3) δ: 2.42 (3H, s), 3.85 (3H, s), 4.58 (2H, d, J=5.6 Hz), 6.27-6.41 (3H, br m), 6.55-6.61 (3H, m), 6.97-7.01 (2H, m), 7.15 (1H, d, J=8.3 Hz), 7.31 (2H, d, J=8.8 Hz), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 334 mg of 4-(2,6-dimethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 5 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 295 mg of N-[4-(2,6-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 163).
The present compound 163
1H-NMR (CDCl3) δ: 2.12 (6H, s), 4.53 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.72-6.76 (2H, m), 7.04-7.12 (3H, m), 7.22 (2H, d, J=8.8 Hz), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.15 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.20 g of 2-aminonicotinic acid, 0.35 g of WSC, 0.50 g of 4-(4-bromophenoxy)benzylamine hydroxide, 2 ml of pyridine and 2 ml of DMF was stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.26 g of N-[4-(4-bromophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 164).
The present compound 164
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.86-6.90 (2H, m), 6.97-7.01 (2H, m), 7.30-7.34 (2H, m), 7.42-7.45 (2H, m), 7.60 (1H, dd, J=7.6, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.16 g of ethyl iodide, 0.42 g of cesium carbonate and 1 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.22 g of N-(3-ethoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 165).
The present compound 165
1H-NMR (CDCl3) δ: 1.41 (3H, t, J=7.0 Hz), 4.03 (2H, q, J=7.0 Hz), 4.57 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.82-6.91 (3H, m), 7.24-7.28 (1H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.12 g of 1-bromopropane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.25 g of N-(3-propoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 166).
The present compound 166
1H-NMR (CDCl3) δ: 1.03 (3H, t, J=7.4 Hz), 1.76-1.85 (2H, m), 3.92 (2H, t, J=6.5 Hz), 4.57 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.83-6.92 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.6 Hz), 8.16 (1H, dd, J=4.8, 1.6 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 1-iodobutane, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.25 g of N-(3-butoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 167).
The present compound 167
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.3 Hz), 1.44-1.54 (2H, m), 1.73-1.80 (2H, m), 3.96 (2H, t, J=6.5 Hz), 4.57 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.82-6.91 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.20 g of 1-iodopentane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.31 g of N-(3-pentyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 168).
The present compound 168
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.1 Hz), 1.35-1.47 (4H, m), 1.75-1.81 (2H, m), 3.95 (2H, t, J=6.6 Hz), 4.56 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.82-6.92 (3H, m), 7.25-7.28 (1H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.21 g of 1-iodohexane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.27 g of N-(3-hexyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 169).
The present compound 169
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=7.0 Hz), 1.31-1.37 (4H, m), 1.43-1.49 (2H, m), 1.74-1.81 (2H, m), 3.95 (2H, t, J=6.5 Hz), 4.57 (2H, d, J=5.4 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.82-6.91 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, d, J=6.3 Hz), 8.17 (1H, dd, J=4.8, 1.6 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 1-iodoheptane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.29 g of N-(3-heptyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 170).
The present compound 170
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.8 Hz), 1.25-1.48 (8H, m), 1.74-1.81 (2H, m), 3.95 (2H, t, J=6.6 Hz), 4.57 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.82-6.92 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.10 g of 5-chloro-1-pentyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water, and a saturated saline solution. The resultant was then concentrated under reduced pressure, so as to obtain 0.25 g of N-[3-(4-pentynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 171).
The present compound 171
1H-NMR (CDCl3) δ: 1.96-2.03 (3H, m), 2.38-2.43 (2H, m), 4.05-4.09 (2H, m), 4.57 (2H, d, J=5.4 Hz), 6.31-6.40 (3H, m), 6.56-6.60 (1H, m), 6.83-6.94 (3H, m), 7.25-7.29 (1H, m), 7.60 (1H, d, J=7.8 Hz), 8.15-8.17 (1H, m).
A mixture of 0.24 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.12 g of 6-chloro-1-hexyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at 80° C. for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.29 g of N-[4-(5-hexynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 172).
The present compound 172
1H-NMR (CDCl3) δ: 1.69-1.76 (2H, m), 1.88-1.95 (2H, m), 1.97 (1H, t, J=2.5 Hz), 2.28 (2H, td, J=6.9, 2.6 Hz), 3.99 (2H, t, J=6.3 Hz), 4.53 (2H, d, J=5.3 Hz), 6.22 (1H, br s), 6.35 (2H, br s), 6.57 (1H, dd, J=7.7, 4.8 Hz), 6.86-6.90 (2H, m), 7.24-7.28 (2H, m), 7.56-7.58 (1H, m), 8.15-8.17 (1H, m).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.15 g of 1-bromo-2-pentyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.25 g of N-[3-(2-hexynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 174).
The present compound 174
1H-NMR (CDCl3) δ: 1.12 (3H, t, J=7.6 Hz), 2.18-2.25 (2H, m), 4.58 (2H, d, J=5.6 Hz), 4.67 (2H, t, J=2.2 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.90-6.96 (3H, m), 7.26-7.31 (1H, m), 7.59 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 235 mg of 4-(3-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 129 mg of N-[4-(3-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 175).
The present compound 175
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.8 Hz), 6.27-6.44 (3H, br m), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.87-6.91 (1H, m), 6.97-7.09 (4H, m), 7.23-7.27 (2H, m), 7.32-7.36 (2H, m), 7.61 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 239 mg of 4-(3-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 102 mg of N-[4-(3-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 176).
The present compound 176
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.8 Hz), 6.28-6.42 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.67-6.71 (1H, m), 6.76-6.83 (2H, m), 7.00-7.05 (2H, m), 7.24-7.30 (1H, m), 7.34 (2H, d, J=8.6 Hz), 7.61 (1H, dd, J=7.7, 1.6 Hz), 8.17 (1H, dd, J=4.9, 1.6 Hz).
0.33 g of triethylamine, 0.24 g of 2-amino-6-methylnicotinic acid and 0.89 g of a BOP reagent were successively added to a mixture of 0.32 g of 2-fluoro-3-(4-pentynyloxy)benzylamine hydrochloride and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.23 g of N-[2-fluoro-3-(4-pentynyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 177).
The present compound 177
1H-NMR (CDCl3) δ: 1.98 (1H, t, J=2.6 Hz), 2.01-2.07 (2H, m), 2.38 (3H, s), 2.44 (2H, td, J=7.0, 2.6 Hz), 4.14 (2H, t, J=6.2 Hz), 4.64 (2H, d, J=5.9 Hz), 6.34 (3H, br s), 6.44 (1H, d, J=7.8 Hz), 6.91-7.06 (3H, m), 7.48 (1H, d, J=7.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 308 mg of 4-(3-trifluoromethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 227 mg of N-[4-(3-trifluoromethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 178).
The present compound 178
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.31-6.42 (3H, br m), 6.60 (1H, dd, J=7.8, 4.8 Hz), 7.00-7.04 (2H, m), 7.14-7.18 (1H, m), 7.22-7.25 (1H, m), 7.33-7.38 (3H, m), 7.42-7.47 (1H, m), 7.62 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 293 mg of 4-(3-trifluoromethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 207 mg of N-[4-(3-trifluoromethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 179).
The present compound 179
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.31-6.40 (3H, br m), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.84-6.87 (1H, m), 6.89-6.98 (2H, m), 7.00-7.05 (2H, m), 7.31-7.36 (3H, m), 7.61 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 296 mg of 4-(2-methylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 265 mg of N-[4-(2-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 180).
The present compound 180
1H-NMR (CDCl3) δ: 2.23 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.86-6.92 (3H, m), 7.06-7.10 (1H, m), 7.15-7.19 (1H, m), 7.24-7.29 (3H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 311 mg of 4-(2-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 190 mg of N-[4-(2-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 181).
The present compound 181
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 6.31 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.96 (2H, d, J=8.6 Hz), 7.04-7.21 (4H, m), 7.29 (2H, d, J=8.6 Hz), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
0.38 g of triethylamine, 0.21 g of 2-aminonicotinic acid and 0.86 g of a BOP reagent were successively added to a mixture of 0.36 g of [5-(2-methylphenyloxy)thiophen-2-yl]methylamine hydrochloride and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[5-(2-methylphenyloxy)thiophen-2-yl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 182).
The present compound 182
1H-NMR (CDCl3) δ: 2.31 (3H, s), 4.63 (2H, d, J=5.6 Hz), 6.26 (1H, d, J=3.9 Hz), 6.29 (1H, br s), 6.34 (2H, br s), 6.59 (1H, dd, J=7.8, 4.9 Hz), 6.71 (1H, dd, J=3.7, 0.7 Hz), 7.00-7.07 (2H, m), 7.13-7.23 (2H, m), 7.58 (1H, d, J=7.8 Hz), 8.15-8.18 (1H, m).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 314 mg of 4-(2-trifluoromethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 183 mg of N-[4-(2-methoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 183).
The present compound 183
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.33-6.45 (3H, br m), 6.56-6.60 (1H, m), 6.94 (1H, d, J=8.3 Hz), 6.99-7.03 (2H, m), 7.16-7.21 (1H, m), 7.30-7.34 (2H, m), 7.43-7.48 (1H, m), 7.59-7.63 (1H, m), 7.66-7.70 (1H, m), 8.16 (1H, dd, J=4.9, 1.6 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 340 mg of 4-(4-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 129 mg of N-[4-(4-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 184).
The present compound 184
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.6 Hz), 6.29 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.91-7.00 (4H, m), 7.27-7.34 (4H, m), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.22 g of 2-amino-4,6-dimethylnicotinic acid hydrochloride, 0.20 g of 1-hydroxybenzotriazole, 0.30 g of WSC, 0.25 g of 4-phenoxybenzylamine hydrochloride, 0.30 g of pyridine and 2 ml of DMF was stirred at a room temperature for 8 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.26 g of N-(4-phenoxyphenyl)methyl-2-amino-4,6-dimethylnicotinic acid amide (hereinafter referred to as the present compound 185).
The present compound 185
1H-NMR (CDCl3) δ: 2.26 (3H, s), 2.31 (3H, s), 4.60 (2H, d, J=5.9 Hz), 5.06 (2H, br s), 6.02 (1H, br s), 6.35 (1H, s), 6.96-7.02 (4H, m), 7.09-7.14 (1H, m), 7.29-7.37 (4H, m).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 340 mg of 4-(4-ethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 263 mg of N-[4-(4-ethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 186).
The present compound 186
1H-NMR (CDCl3) δ: 1.42 (3H, t, J=7.0 Hz), 4.02 (2H, q, J=7.0 Hz), 4.55 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.86-6.97 (6H, m), 7.25-7.28 (2H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 355 mg of 4-(4-propoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 217 mg of N-[4-(4-propoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 187).
The present compound 187
1H-NMR (CDCl3) δ: 1.04 (3H, t, J=7.5 Hz), 1.76-1.86 (2H, m), 3.91 (2H, t, J=6.6 Hz), 4.55 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.87-6.97 (6H, m), 7.25-7.28 (2H, m), 7.58 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 367 mg of 4-(3-ethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 290 mg of N-[4-(3-ethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 188).
The present compound 188
1H-NMR (CDCl3) δ: 1.40 (3H, t, J=7.0 Hz), 4.00 (2H, q, J=7.0 Hz), 4.58 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.37 (2H, br s), 6.54-6.67 (4H, m), 7.01 (2H, d, J=8.6 Hz), 7.22 (1H, dd, J=8.1, 8.1 Hz), 7.31 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 349 mg of 4-(3-butoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 226 mg of N-[4-(3-butoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 189).
The present compound 189
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.3 Hz), 1.42-1.52 (2H, m), 1.71-1.78 (2H, m), 3.92 (2H, t, J=6.6 Hz), 4.58 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.36 (2H, br s), 6.55-6.61 (3H, m), 6.63-6.67 (1H, m), 6.99-7.03 (2H, m), 7.19-7.23 (1H, m), 7.31 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.42 g of 4-(indan-5-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.29 g of N-[4-(indan-5-yloxy)]phenylmethyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 190).
The present compound 190
1H-NMR (CDCl3) δ: 2.06-2.14 (2H, m), 2.88 (4H, t, J=7.5 Hz), 4.56 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.34-6.37 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.79 (1H, dd, J=8.2, 2.1 Hz), 6.87 (1H, d, J=2.1 Hz), 6.95-6.99 (2H, m), 7.17 (1H, d, J=8.2 Hz), 7.26-7.31 (2H, m), 7.59 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.38 g of 4-(benzo[1,3]dioxol-5-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.19 g of N-[4-(benzo[1,3]dioxol-5-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 191).
The present compound 191
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 5.98 (2H, s), 6.25 (1H, br s), 6.36 (2H, br s), 6.49 (1H, dd, J=8.3, 2.3 Hz), 6.57-6.60 (2H, m), 6.76 (1H, d, J=8.3 Hz), 6.92-6.96 (2H, m), 7.26-7.30 (2H, m), 7.59 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.39 g of 4-(2-naphthyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.27 g of N-[4-(2-naphthyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 192).
The present compound 192
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.29-6.41 (3H, br m), 6.59 (1H, dd, J=7.7, 4.8 Hz), 7.03-7.08 (2H, m), 7.23-7.27 (1H, m), 7.30-7.37 (3H, m), 7.39-7.49 (2H, m), 7.61 (1H, dd, J=7.7, 1.7 Hz), 7.70 (1H, d, J=8.1 Hz), 7.83 (1H, d, J=7.8 Hz), 7.84 (1H, d, J=8.8 Hz), 8.17 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.33 g of 4-(pyridin-3-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.06 g of N-[4-(pyridin-3-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 193).
The present compound 193
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.6 Hz), 6.37 (2H, br s), 6.45 (1H, br s), 6.59 (1H, dd, J=7.6, 4.8 Hz), 6.99-7.03 (2H, m), 7.25-7.35 (4H, m), 7.62 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz), 8.35-8.39 (2H, m).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 4-methoxybutane methanesulfonate, 0.42 g of cesium carbonate and 3 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.24 g of N-[3-(4-methoxybutoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 194).
The present compound 194
1H-NMR (CDCl3) δ: 1.72-1.89 (4H, m), 3.34 (3H, s), 3.44 (2H, t, J=6.2 Hz), 3.98 (2H, t, J=6.2 Hz), 4.57 (2H, d, J=5.6 Hz), 6.26 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.82-6.93 (3H, m), 7.26-7.31 (1H, m), 7.59 (1H, d, J=7.7 Hz), 8.17 (1H, d, J=4.8 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.27 g of 4-ethoxybutan-p-toluenesulfonate, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.26 g of N-[3-(4-ethoxybutoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 195).
The present compound 195
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.1 Hz), 1.72-1.90 (4H, m), 3.46-3.51 (4H, m), 3.99 (2H, t, J=6.3 Hz), 4.57 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.82-6.92 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.17 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 3-ethoxypropane methanesulfonate, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.25 g of N-[3-(3-ethoxypropoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 196).
The present compound 196
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.1 Hz), 2.02-2.08 (2H, m), 3.49 (2H, q, J=7.1 Hz), 3.59 (2H, t, J=6.2 Hz), 4.06 (2H, t, J=6.2 Hz), 4.57 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.83-6.92 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.6, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
0.55 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.18 g of 3-phenylmethylbenzylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure, so as to obtain 0.18 g of N-[(3-phenylmethyl)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 197).
The present compound 197
1H-NMR (CDCl3) δ: 3.98 (2H, s), 4.56 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.38 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 7.13-7.31 (9H, m), 7.56 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
0.33 g of 2-chloro-6-methylnicotinic acid chloride, 0.30 g of 4-(3-methylphenoxy)benzylamine, 0.50 g of triethylamine and 10 ml of THF were stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then subjected to silica gel column chromatography, so as to obtain 0.40 g of N-[4-(3-methylphenoxy)phenyl]methyl-2-chloro-6-methylnicotinic acid amide.
0.40 g of the thus obtained N-[4-(3-methylphenoxy)phenyl]methyl-2-chloro-6-methylnicotinic acid amide, 1 ml of 1,4-dioxane and 4 ml of 28% aqueous ammonia were mixed. The obtained mixture was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 120° C. for 5 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then subjected to silica gel column chromatography, so as to obtain 0.27 g of N-[4-(3-methylphenoxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 198).
The present compound 198
1H-NMR (CDCl3) δ: 2.33 (3H, s), 2.38 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.38 (2H, br s), 6.44 (1H, d, J=7.9 Hz), 6.78-6.84 (2H, m), 6.90-7.00 (3H, m), 7.19-7.30 (3H, m), 7.49 (1H, d, J=7.9 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.15 g of 5-bromo-1-pentene, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The extract was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.26 g of N-[3-(4-heptenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 199).
The present compound 199
1H-NMR (CDCl3) δ: 1.84-1.92 (2H, m), 2.20-2.26 (2H, m), 3.97 (2H, t, J=6.4 Hz), 4.57 (2H, d, J=5.6 Hz), 4.98-5.09 (2H, m), 5.79-5.89 (1H, m), 6.27 (1H, br s), 6.35 (2H, br s), 6.58 (1H, dd, J=7.6, 5.0 Hz), 6.83-6.92 (3H, m), 7.24-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.15 g of 6-bromo-1-hexene, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The extract was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.27 g of N-[3-(5-hexenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 200).
The present compound 200
1H-NMR (CDCl3) δ: 1.53-1.61 (2H, m), 1.76-1.83 (2H, m), 2.10-2.15 (2H, m), 3.96 (2H, t, J=6.5 Hz), 4.56 (2H, d, J=5.6 Hz), 4.95-5.05 (2H, m), 5.77-5.88 (1H, m), 6.30 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.5, 4.8 Hz), 6.82-6.92 (3H, m), 7.23-7.29 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.8, 1.9 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 309 mg of 3-(2-methylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 163 mg of N-[3-(2-methylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 201).
The present compound 201
1H-NMR (CDCl3) δ: 2.23 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.26-6.38 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 6.77-6.82 (1H, m), 6.88-6.94 (2H, m), 7.00-7.03 (1H, m), 7.06-7.11 (1H, m), 7.15-7.20 (1H, m), 7.24-7.30 (2H, m), 7.58 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 320 mg of 3-(2-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 277 mg of N-[3-(2-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 202).
The present compound 202
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.27-6.41 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.86-6.90 (1H, m), 6.94-6.98 (1H, m), 7.03-7.22 (5H, m), 7.28-7.33 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 337 mg of 3-(2-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 254 mg of N-[3-(2-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 203).
The present compound 203
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.27-6.42 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 6.89-6.99 (4H, m), 7.07-7.11 (1H, m), 7.27-7.35 (3H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 336 mg of 3-(3-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 297 mg of N-[3-(3-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 204).
The present compound 204
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.29-6.39 (3H, br m), 6.60 (1H, dd, J=7.6, 4.8 Hz), 6.88-6.92 (1H, m), 6.92-6.96 (1H, m), 6.97-7.02 (2H, m), 7.06-7.15 (2H, m), 7.25-7.28 (1H, m), 7.32-7.37 (1H, m), 7.60 (1H, d, J=7.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 389 mg of 3-(3-trifluoromethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 259 mg of N-[3-(3-trifluoromethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 205).
The present compound 205
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.32-6.40 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 6.93-6.97 (1H, m), 7.00-7.03 (1H, m), 7.12-7.19 (2H, m), 7.23-7.27 (1H, m), 7.34-7.39 (2H, m), 7.42-7.47 (1H, m), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 401 mg of 3-(3-trifluoromethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 175 mg of N-[3-(3-trifluoromethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 206).
The present compound 206
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.30-6.41 (3H, br m), 6.59 (1H, dd, J=7.8, 4.9 Hz), 6.85-6.87 (1H, m), 6.90-6.99 (3H, m), 7.01-7.03 (1H, m), 7.11-7.16 (1H, m), 7.32 (1H, d, J=8.3 Hz), 7.37 (1H, d, J=8.1 Hz), 7.60 (1H, dd, J=7.8, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 354 mg of 3-(3-ethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 269 mg of N-[3-(3-ethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 207).
The present compound 207
1H-NMR (CDCl3) δ: 1.39 (3H, t, J=6.9 Hz), 3.99 (2H, q, J=6.9 Hz), 4.58 (2H, d, J=5.8 Hz), 6.27-6.38 (3H, br m), 6.55-6.60 (3H, m), 6.64-6.67 (1H, m), 6.92-6.96 (1H, m), 6.99-7.01 (1H, m), 7.05-7.09 (1H, m), 7.19-7.24 (1H, m), 7.29-7.34 (1H, m), 7.59 (1H, dd, J=7.7, 1.7 Hz), 8.16 (1H, dd, J=5.1, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 336 mg of 3-(3-ethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 160 mg of N-[3-(3-ethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 208).
The present compound 208
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.7 Hz), 2.63 (2H, q, J=7.7 Hz), 4.57 (2H, d, J=5.6 Hz), 6.29-6.39 (3H, br m), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.80-6.84 (1H, m), 6.86-6.88 (1H, m), 6.90-6.99 (3H, m), 7.04-7.08 (1H, m), 7.22-7.27 (1H, m), 7.28-7.32 (1H, m), 7.58 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 303 mg of 3-(3-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 142 mg of N-[3-(3-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 209).
The present compound 209
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.29-6.40 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9
Hz), 6.68-6.72 (1H, m), 6.77-6.83 (2H, m), 6.94-6.98 (1H, m), 7.01-7.03 (1H, m), 7.11-7.14 (1H, m), 7.24-7.31 (1H, m), 7.32-7.37 (1H, m), 7.60 (1H, dd, J=7.7, 1.6 Hz), 8.17 (1H, dd, J=4.9, 1.6 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.10 g of 5-chloro-1-pentyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.22 g of N-[2-fluoro-3-(4-pentynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 210).
The present compound 210
1H-NMR (CDCl3) δ: 1.98 (1H, t, J=2.7 Hz), 2.01-2.07 (2H, m), 2.44 (2H, td, J=6.9, 2.6 Hz), 4.15 (2H, t, J=6.1 Hz), 4.65 (2H, d, J=5.1 Hz), 6.33 (2H, br s), 6.38 (1H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.91-7.08 (3H, m), 7.59 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 312 mg of 3-(4-fluorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 152 mg of N-[3-(4-fluorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 211).
The present compound 211
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.29-6.39 (3H, br m), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.85-6.89 (1H, m), 6.94-7.08 (6H, m), 7.28-7.32 (1H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 339 mg of 3-(4-chlorophenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 145 mg of N-[3-(4-chlorophenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 212).
The present compound 212
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.29-6.37 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 6.89-6.98 (4H, m), 7.07-7.11 (1H, m), 7.26-7.34 (3H, m), 7.59 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 349 mg of 3-(4-trifluoromethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 125 mg of N-[3-(4-trifluoromethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 213).
The present compound 213
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.6 Hz), 6.31-6.40 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 6.90-6.94 (1H, m), 6.98-7.03 (3H, m), 7.09-7.12 (1H, m), 7.16-7.21 (2H, m), 7.31-7.36 (1H, m), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 329 mg of 3-(4-ethoxyphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 119 mg of N-[3-(4-ethoxyphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 214).
The present compound 214
1H-NMR (CDCl3) δ: 1.42 (3H, t, J=7.0 Hz), 4.02 (2H, q, J=7.0 Hz), 4.55 (2H, d, J=5.8 Hz), 6.24-6.37 (3H, br m), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.83-6.92 (4H, m), 6.94-7.02 (3H, m), 7.25-7.29 (1H, m), 7.57 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 328 mg of 3-(4-ethylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 136 mg of N-[3-(4-ethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 215).
The present compound 215
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.6 Hz), 2.64 (2H, q, J=7.6 Hz), 4.57 (2H, d, J=5.8 Hz), 6.26-6.38 (3H, br m), 6.58 (1H, dd, J=7.6, 4.8 Hz), 6.88-6.97 (4H, m), 7.02-7.05 (1H, m), 7.15-7.19 (2H, m), 7.27-7.31 (1H, m), 7.58 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 248 mg of 2-aminonicotinic acid, 203 mg of 1-hydroxybenzotriazole, 430 mg of WSC, 348 mg of 3-(4-propylphenoxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 232 mg of N-[3-(4-propylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 216).
The present compound 216
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.3 Hz), 1.59-1.68 (2H, m), 2.55-2.59 (2H, m), 4.57 (2H, d, J=5.8 Hz), 6.26-6.37 (3H, br m), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.88-6.97 (4H, m), 7.02-7.06 (1H, m), 7.12-7.16 (2H, m), 7.27-7.31 (1H, m), 7.58 (1H, dd, J=7.7, 1.8 Hz), 8.16 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.32 g of 3-phenylthiobenzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.26 g of N-(3-phenylthiophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 217).
The present compound 217
1H-NMR (CDCl3) δ: 4.55 (2H, d, J=5.6 Hz), 6.22-6.38 (3H, br m), 6.58 (1H, dd, J=7.7, 4.9 Hz), 7.18-7.39 (9H, m), 7.54 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.30 g of 4-phenylthiobenzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.24 g of N-(4-phenylthiophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 218).
The present compound 218
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.26-6.39 (3H, br m), 6.59 (1H, dd, J=7.8, 4.8 Hz), 7.23-7.39 (9H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.17 (1H, dd, J=4.8, 1.7 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.33 g of 3-(indan-5-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.24 g of N-[3-(indan-5-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 219).
The present compound 219
1H-NMR (CDCl3) δ: 2.05-2.14 (2H, m), 2.85-2.91 (4H, m), 4.56 (2H, d, J=5.8 Hz), 6.26 (1H, br s), 6.34 (2H, br s), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.78-6.82 (1H, m), 6.87-6.92 (2H, m), 6.95-6.96 (1H, m), 7.01-7.05 (1H, m), 7.15-7.19 (1H, m), 7.27-7.31 (1H, m), 7.58 (1H, dd, J=7.7, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.37 g of 3-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.18 g of N-[3-(5,6,7,8-tetrahydronaphthalen-2-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 220).
The present compound 220
1H-NMR (CDCl3) δ: 1.76-1.82 (4H, m), 2.70-2.76 (4H, m), 4.56 (2H, d, J=5.8 Hz), 6.27 (1H, br s), 6.34 (2H, br s), 6.58 (1H, dd, J=7.6, 4.9 Hz), 6.72-6.78 (2H, m), 6.89-6.92 (1H, m), 6.95-6.97 (1H, m), 7.01-7.05 (2H, m), 7.27-7.31 (1H, m), 7.58 (1H, dd, J=7.6, 1.8 Hz), 8.17 (1H, dd, J=4.9, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.35 g of 3-[benzo[1,3]dioxol-5-yloxy]benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.16 g of N-[3-(benzo[1,3]dioxol-5-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 221).
The present compound 221
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.6 Hz), 5.98 (2H, s), 6.28 (1H, br s), 6.33 (2H, br s), 6.50 (1H, dd, J=8.5, 2.4 Hz), 6.56-6.61 (2H, m), 6.76 (1H, d, J=8.3 Hz), 6.87 (1H, dd, J=8.0, 2.1 Hz), 6.92-6.94 (1H, m), 7.01-7.04 (1H, m), 7.26-7.31 (1H, m), 7.58 (1H, dd, J=7.6, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.39 g of 3-(2-naphthyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.27 g of N-[3-(2-naphthyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 222).
The present compound 222
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.8 Hz), 6.26-6.34 (3H, br m), 6.56 (1H, dd, J=7.7, 4.9 Hz), 6.97-7.01 (1H, m), 7.03-7.05 (1H, m), 7.09-7.13 (1H, m), 7.23-7.27 (1H, m), 7.32-7.37 (2H, m), 7.40-7.49 (2H, m), 7.57 (1H, dd, J=7.7, 1.7 Hz), 7.71 (1H, d, J=8.1 Hz), 7.81-7.86 (2H, m), 8.16 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.29 g of 3-(pyridin-3-yloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.05 g of N-[3-(pyridin-3-yloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 223).
The present compound 223
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.34 (2H, br s), 6.40 (1H, br s), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.94 (1H, dd, J=7.8, 2.0 Hz), 7.01-7.02 (1H, m), 7.12-7.15 (1H, m), 7.26-7.37 (3H, m), 7.61 (1H, dd, J=7.7, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz), 8.36-8.40 (2H, m).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 1-iodobutane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.27 g of N-(2-fluoro-3-butoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 210).
The present compound 224
1H-NMR (CDCl3) δ: 0.98 (3H, t, J=7.3 Hz), 1.47-1.56 (2H, m), 1.77-1.85 (2H, m), 4.03 (2H, t, J=6.5 Hz), 4.64 (2H, d, J=5.4 Hz), 6.32 (2H, br s), 6.39 (1H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.90-7.05 (3H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.20 g of 1-iodopentane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.25 g of N-(2-fluoro-3-pentyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 225).
The present compound 225
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.2 Hz), 1.34-1.50 (4H, m), 1.79-1.87 (2H, m), 4.02 (2H, t, J=6.7 Hz), 4.64 (2H, d, J=5.1 Hz), 6.33 (2H, br s), 6.39 (1H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.89-7.05 (3H, m), 7.59 (1H, dd, J=7.6, 1.7 Hz), 8.15 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.21 g of 1-iodohexane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution and water, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.27 g of N-(2-fluoro-3-hexyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 226).
The present compound 226
1H-NMR (CDCl3) δ: 0.91 (3H, t, J=6.3 Hz), 1.33-1.49 (6H, m), 1.78-1.86 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.65 (2H, d, J=5.9 Hz), 6.33 (2H, br s), 6.39 (1H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.89-7.05 (3H, m), 7.57-7.61 (1H, m), 8.14-8.17 (1H, m).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.18 g of 1-iodoheptane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the precipitated solid was then collected by filtration. The collected solid was successively washed with water and hexane, so as to obtain 0.23 g of N-(2-fluoro-3-heptyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 227).
The present compound 227
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=6.8 Hz), 1.25-1.50 (8H, m), 1.78-1.86 (2H, m), 4.02 (2H, t, J=6.6 Hz), 4.64 (2H, d, J=5.4 Hz), 6.32 (2H, br s), 6.39 (1H, br s), 6.58 (1H, dd, J=7.7, 4.8 Hz), 6.89-7.05 (3H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.25 g of 2-fluoro-3-phenoxybenzylamine hydrochloride, 0.13 g of 2-aminonicotinic acid, 0.24 g of WSC and 3 ml of pyridine was stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a sodium hydroxide aqueous solution, water and hexane, so as to obtain 0.16 g of N-(2-fluoro-3-phenoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 228).
The present compound 228
1H-NMR (CDCl3) δ: 4.69 (2H, d, J=5.1 Hz), 6.33 (1H, br s), 6.43 (2H, br s), 6.60 (1H, dd, J=7.2, 5.6 Hz), 7.00 (2H, d, J=7.7 Hz), 7.05-7.19 (4H, m), 7.29-7.37 (2H, m), 7.61 (1H, d, J=7.7 Hz), 8.17 (1H, d, J=4.6 Hz).
0.21 g of 2-aminonicotinic acid, 0.23 g of 2-fluorobenzylamine, 0.80 g of a BOP reagent and 0.21 g of triethylamine were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.30 g of N-(2-fluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 229).
The present compound 229
1H-NMR (CDCl3) δ: 4.65 (2H, d, J=5.9 Hz), 6.26-6.48 (3H, br m), 6.59 (1H, dd, J=7.7, 4.9 Hz), 7.05-7.15 (2H, m), 7.26-7.32 (1H, m), 7.37-7.43 (1H, m), 7.60 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.9, 1.8 Hz).
0.21 g of 2-aminonicotinic acid, 0.26 g of 2-chlorobenzylamine, 0.80 g of a BOP reagent and 0.20 g of triethylamine were added to 3 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.32 g of N-(2-chlorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 230).
The present compound 230
1H-NMR (CDCl3) δ: 4.68 (2H, d, J=5.9 Hz), 6.33 (2H, br s), 6.54 (1H, br s), 6.59 (1H, dd, J=7.7, 4.9 Hz), 7.25-7.27 (2H, m), 7.38-7.45 (2H, m), 7.61 (1H, dd, J=7.7, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
0.21 g of 2-aminonicotinic acid, 0.32 g of 3-trifluoromethylbenzylamine, 0.80 g of a BOP reagent and 0.20 g of triethylamine were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 6 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.40 g of N-(3-trifluoromethylphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 231).
The present compound 231
1H-NMR (CDCl3) δ: 4.66 (2H, d, J=5.9 Hz), 6.37 (2H, br s), 6.42 (1H, br s), 6.60 (1H, dd, J=7.7, 4.9 Hz), 7.49-7.59 (4H, m), 7.62 (1H, dd, J=7.7, 1.7 Hz), 8.18 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.19 g of 1-iodopropane, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution and water, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.21 g of N-(2-fluoro-3-propyloxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 232).
The present compound 232
1H-NMR (CDCl3) δ: 1.06 (3H, t, J=7.4 Hz), 1.83-1.89 (2H, m), 3.99 (2H, t, J=6.6 Hz), 4.65 (2H, d, J=5.6 Hz), 6.34 (2H, br s), 6.39 (1H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.90-7.06 (3H, m), 7.60 (1H, d, J=7.8 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.13 g of 3-bromo-1-propene, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution and water, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 0.21 g of N-[2-fluoro-3-(2-propenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 233).
The present compound 233
1H-NMR (CDCl3) δ: 4.61 (2H, dt, J=5.4, 1.5 Hz), 4.65 (2H, d, J=5.6 Hz), 5.30-5.34 (1H, m), 5.41-5.47 (1H, m), 6.01-6.11 (1H, m), 6.33 (2H, br s), 6.42 (1H, br s), 6.58 (1H, dd, J=7.8, 4.9 Hz), 6.90-7.05 (3H, m), 7.59 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.24 g of N-(3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.13 g of 3-bromo-1-propyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.23 g of N-[3-(2-propynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 234).
The present compound 234
1H-NMR (CDCl3) δ: 2.51 (1H, t, J=2.3 Hz), 4.59 (2H, d, J=5.6 Hz), 4.70 (2H, d, J=2.4 Hz), 6.30 (1H, br s), 6.36 (2H, br s), 6.59 (1H, dd, J=7.8, 4.9 Hz), 6.90-6.99 (3H, m), 7.28-7.33 (1H, m), 7.60 (1H, dd, J=7.8, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
A mixture of 0.26 g of N-(2-fluoro-3-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.13 g of 3-bromo-1-propyne, 0.42 g of cesium carbonate and 2 ml of DMF was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution. The resultant was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.13 g of N-[2-fluoro-3-(2-propynyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 235).
The present compound 235
1H-NMR (CDCl3) δ: 2.55 (1H, t, J=2.3 Hz), 4.66 (2H, m), 4.77 (2H, d, J=2.4 Hz), 6.33 (1H, br s), 6.40 (2H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 7.02-7.09 (3H, m), 7.59 (1H, dd, J=7.7, 1.6 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.21 g of 2-aminonicotinic acid, 0.26 g of 2,6-difluorobenzylamine, 0.80 g of a BOP reagent and 0.20 g of triethylamine were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with a sodium bicarbonate aqueous solution and MTBE, and it was then dried, so as to obtain 0.12 g of N-(2,6-difluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 237).
The present compound 237
1H-NMR (CDCl3) δ: 4.71 (2H, d, J=5.9 Hz), 6.32 (2H, br s), 6.36 (1H, br s), 6.58 (1H, dd, J=7.7, 4.9 Hz), 6.90-6.96 (2H, m), 7.24-7.30 (1H, m), 7.57 (1H, dd, J=7.7, 1.8 Hz), 8.15 (1H, dd, J=4.9, 1.8 Hz).
0.21 g of 2-aminonicotinic acid, 0.26 g of 3,5-difluorobenzylamine, 0.80 g of a BOP reagent and 0.20 g of triethylamine were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with a sodium bicarbonate aqueous solution and MTBE, and it was then dried, so as to obtain 0.12 g of N-(3,5-difluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 238).
The present compound 238
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.9 Hz), 6.37 (2H, br s), 6.40 (1H, br s), 6.61 (1H, dd, J=7.7, 4.9 Hz), 6.74 (1H, tt, J=8.9, 2.2 Hz), 6.86 (2H, d, J=6.1 Hz), 7.63 (1H, dd, J=7.7, 1.7 Hz), 8.19 (1H, dd, J=4.9, 1.7 Hz).
0.21 g of 2-aminonicotinic acid, 0.26 g of 3,4-difluorobenzylamine, 0.80 g of a BOP reagent and 0.20 g of triethylamine were added to 2 ml of DMF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with a sodium bicarbonate aqueous solution and MTBE, and it was then dried, so as to obtain 0.12 g of N-(3,4-difluorophenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 239).
The present compound 239
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.9 Hz), 6.35 (3H, br m), 6.60 (1H, dd, J=7.7, 4.8 Hz), 7.04-7.08 (1H, m), 7.11-7.19 (2H, m), 7.61 (1H, dd, J=7.7, 1.7 Hz), 8.18 (1H, dd, J=4.8, 1.7 Hz).
0.86 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.23 g of 2-amino-6-methylnicotinic acid, 0.33 g of [5-(3-methylphenyloxy)thiophen-2-yl]methylamine and 2 ml of DMF. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was subjected to silica gel column chromatography, so as to obtain 0.36 g of N-[5-(3-methylphenoxy)thiophen-2-yl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 241).
The present compound 241
1H-NMR (CDCl3) δ: 2.33 (3H, s), 2.38 (3H, s), 4.64 (2H, d, J=5.4 Hz), 6.28 (1H, br s), 6.35-6.38 (3H, m), 6.44 (1H, d, J=7.8 Hz), 6.73 (1H, d, J=3.9 Hz), 6.87-6.94 (3H, m), 7.18-7.22 (1H, m), 7.48 (1H, d, J=7.8 Hz).
0.58 g of a BOP reagent and 0.25 g of triethylamine were successively added to a mixture of 0.13 g of 2-aminonicotinic acid, 0.25 g of 2-fluoro-5-phenoxybenzylamine hydrochloride and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 20 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with water and hexane, so as to obtain 0.22 g of N-(2-fluoro-5-phenoxyphenyl)methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 243).
The present compound 243
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.9 Hz), 6.31 (2H, br s), 6.41 (1H, br s), 6.59 (1H, dd, J=7.8, 4.9 Hz), 6.88-7.12 (6H, m), 7.31-7.36 (2H, m), 7.58 (1H, dd, J=7.8, 1.7 Hz), 8.15 (1H, dd, J=4.9, 1.7 Hz).
0.86 g of a BOP reagent and 0.20 g of triethylamine were successively added to a mixture of 0.23 g of 2-amino-6-methylnicotinic acid, 0.33 g of [5-(4-methylphenyloxy)thiophen-2-yl]methylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The obtained extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatograph, so as to obtain 0.12 g of N-[5-(4-methylphenoxy)thiophen-2-yl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 244).
The present compound 244
1H-NMR (CDCl3) δ: 2.32 (3H, s), 2.38 (3H, s), 4.63 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.34 (1H, d, J=3.7 Hz), 6.37 (2H, br s), 6.44 (1H, d, J=7.8 Hz), 6.71 (1H, d, J=3.7 Hz), 6.97-7.01 (2H, m), 7.10-7.14 (2H, m), 7.48 (1H, d, J=7.8 Hz).
0.56 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.27 g of 3-(4-trifluoromethylphenoxy)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The obtained extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatograph, so as to obtain 0.33 g of N-[3-(4-trifluoromethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 247).
The present compound 247
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.9 Hz), 6.38 (3H, br s), 6.60 (1H, dd, J=7.6, 4.9 Hz), 6.97 (1H, dd, J=7.9, 2.1 Hz), 7.03-7.07 (3H, m), 7.16 (1H, d, J=8.0 Hz), 7.35-7.39 (1H, m), 7.56-7.63 (3H, m), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.58 g of a BOP reagent and 0.13 g of triethylamine were successively added to a mixture of 0.14 g of 2-aminonicotinic acid, 0.23 g of 4-(3,5-dimethylphenoxy)benzylamine and 3 ml of DMF. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, water and a saturated sodium bicarbonate solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The obtained extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatograph, so as to obtain 0.18 g of N-[4-(3,5-dimethylphenoxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 248).
The present compound 248
1H-NMR (CDCl3) δ: 2.28 (6H, d, J=0.5 Hz), 4.57 (2H, d, J=5.6 Hz), 6.27 (1H, br s), 6.37 (2H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.62-6.63 (2H, m), 6.75-6.77 (1H, m), 6.96-7.01 (2H, m), 7.28-7.32 (2H, m), 7.60 (1H, dd, J=7.6, 1.7 Hz), 8.16 (1H, dd, J=4.9, 1.7 Hz).
0.25 g of triethylamine was added to a mixture solution of 0.14 g of 2-aminonicotinic acid, 0.31 g of [5-(3-trifluoromethylphenyloxy)thiophen-2-yl]methylamine hydrochloride and 3 ml of DMF. Subsequently, 0.57 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 20 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a sodium bicarbonate aqueous solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was washed with hexane, so as to obtain 0.30 g of N-[5-(3-trifluoromethylphenoxy)thiophen-2-yl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 249).
The present compound 249
1H-NMR (CDCl3) δ: 4.67 (2H, d, J=5.9 Hz), 6.35 (1H, br s), 6.40 (2H, br s), 6.45 (1H, d, J=3.9 Hz), 6.60 (1H, dd, J=7.8, 4.9 Hz), 6.78 (1H, d, J=3.9 Hz), 7.24-7.46 (4H, m), 7.61 (1H, dd, J=7.8, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
0.81 ml of a 28% sodium methoxide in methanol was added to a mixture of 0.33 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide and 3 ml of N-methyl-2-pyrrolidone. The obtained mixture was then stirred at 130° C. for 12 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.17 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methoxynicotinic acid amide (hereinafter referred to as the present compound 250).
The present compound 250
1H-NMR (CDCl3) δ: 3.87 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.00 (1H, d, J=8.5 Hz), 6.12 (1H, br s), 6.53 (2H, br s), 6.97-7.01 (4H, m), 7.10 (1H, t, J=7.44 Hz), 7.29-7.35 (4H, m), 7.50 (1H, d, J=8.5 Hz).
A mixture of 0.29 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide, 0.68 ml of propylamine and 2.5 ml of N-methyl-2-pyrrolidone was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 150° C. for 30 minutes. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.11 g of N-(4-phenoxyphenyl)methyl-2-amino-6-propylaminonicotinic acid amide (hereinafter referred to as the present compound 251).
The present compound 251
1H-NMR (CDCl3) δ: 0.97 (3H, t, J=7.5 Hz), 1.57-1.64 (2H, m), 3.21 (2H, dd, J=13.0, 7.0 Hz), 4.54 (2H, d, J=5.6 Hz), 4.62 (1H, br s), 5.68 (1H, d, J=8.7 Hz), 5.99 (1H, br s), 6.43 (2H, br s), 6.98-7.00 (4H, m), 7.09-7.11 (1H, m), 7.27-7.35 (5H, m).
0.31 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide was added to a mixture of 0.18 g of 60% sodium hydride (in oil), 0.66 ml of propyl alcohol and 3 ml of N-methyl-2-pyrrolidone. The obtained mixture was stirred at 130° C. for 5 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was dried under reduced pressure, so as to obtain 0.23 g of N-(4-phenoxyphenyl)methyl-2-amino-6-propoxynicotinic acid amide (hereinafter referred to as the present compound 252).
The present compound 252
1H-NMR (CDCl3) δ: 1.00 (3H, t, J=7.4 Hz), 1.74-1.78 (2H, m), 4.19 (2H, t, J=6.8 Hz), 4.55 (2H, d, J=5.6 Hz), 5.99 (1H, d, J=8.5 Hz), 6.08 (1H, br s), 6.50 (2H, br s), 6.98-6.99 (4H, m), 7.10-7.11 (1H, m), 7.27-7.34 (4H, m), 7.49 (1H, d, J=8.5 Hz).
A mixture of 0.30 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide, 0.38 g of 2,4-dichlorothiazole, 0.60 g of cesium carbonate and 8 ml of DMF was heated to reflux for 2 hours. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.34 g of N-4-(4-chlorothiazol-2-yloxy)phenylmethyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 253).
The present compound 253
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.9 Hz), 6.37 (2H, br s), 6.43 (1H, br s), 6.60 (2H, dd, J=7.9, 4.5 Hz), 7.24-7.27 (2H, m), 7.36-7.39 (2H, m), 7.63 (1H, dd, J=7.6, 1.7 Hz), 8.17 (1H, dd, J=4.9, 1.7 Hz).
0.58 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide was added to a mixture of 0.26 g of 60% sodium hydride (in oil), 0.75 ml of butyl alcohol and 5 ml of N-methyl-2-pyrrolidone. The obtained mixture was stirred at 120° C. for 13 hours 30 minutes. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.39 g of N-(4-phenoxyphenyl)methyl-2-amino-6-butoxynicotinic acid amide (hereinafter referred to as the present compound 254).
The present compound 254
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.45 (2H, m), 1.68-1.75 (2H, m), 4.23 (2H, t, J=6.8 Hz), 4.55 (2H, d, J=5.8 Hz), 5.98 (1H, d, J=8.2 Hz), 6.07 (1H, br s), 6.50 (2H, br s), 6.99-7.00 (4H, m), 7.10-7.11 (1H, m), 7.24-7.36 (4H, m), 7.49 (1H, d, J=8.2 Hz).
0.32 g of 2-amino-3-cyano-5-fluoropyridine and 5 ml of concentrated sulfuric acid were added to 5 ml of water and the obtained mixture was heated to reflux for 6 hours 30 minutes. Thereafter, aqueous ammonia was added to the reaction mixture, so that the pH was adjusted to pH 10. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-5-fluoronicotinic acid.
The thus obtained crude 2-amino-5-fluoronicotinic acid, 0.81 g of 4-phenoxybenzylamine hydrochloride and 0.85 ml of triethylamine were added to 5 ml of DMF. Thereafter, 1.22 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 5 hours. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, so as to obtain 0.43 g of N-(4-phenoxyphenyl)methyl-2-amino-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 255).
The present compound 255
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.18 (2H, br s), 6.24 (1H, br s), 6.97-7.02 (4H, m), 7.12 (1H, t, J=7.4 Hz), 7.30-7.34 (5H, m), 8.07 (1H, d, J=2.7 Hz).
0.22 g of 2-amino-3-cyano-5-fluoropyridine and 1.5 ml of concentrated sulfuric acid were added to 4.5 ml of water, and the obtained mixture was heated to reflux for 8 hours. Thereafter, aqueous ammonia was added to the reaction mixture, so that the pH was adjusted to pH 10. The reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-5-fluoronicotinic acid.
The thus obtained crude 2-amino-5-fluoronicotinic acid, 0.47 g of 2-fluoro-3-(5-hexynyl)oxybenzylamine hydrochloride and 0.59 ml of triethylamine were added to 5 ml of DMF. Thereafter, 0.86 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, and it was then subjected to silica gel column chromatography and recrystallization using a mixed solvent of hexane and ethyl acetate, so as to obtain 0.21 g of N-[2-fluoro-3-(4-hexynyl)oxy]methyl-2-amino-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 256).
The present compound 256
1H-NMR (CDCl3) δ: 1.99-2.06 (3H, m), 2.44-2.46 (2H, m), 4.15 (2H, t, J=6.2 Hz), 4.64 (2H, d, J=5.8 Hz), 6.15 (2H, br s), 6.38 (1H, br s), 6.95 (2H, m), 7.05 (1H, td, J=7.9, 1.5 Hz), 7.38 (1H, dd, J=8.3, 2.9 Hz), 8.06 (1H, d, J=2.9 Hz).
0.27 g of 2-amino-3-cyano-5-fluoropyridine and 2 ml of concentrated sulfuric acid were added to 4 ml of water, and the obtained mixture was heated to reflux for 7 hours 30 minutes. Thereafter, aqueous ammonia was added to the reaction mixture, so that the pH was adjusted to pH 10. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-5-fluoronicotinic acid.
The thus obtained crude 2-amino-5-fluoronicotinic acid, 0.34 g of 2-fluoro-3-methoxybenzylamine and 0.73 ml of triethylamine were added to 5 ml of DMF. Thereafter, 1.06 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 8 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, so as to obtain 0.34 g of N-[(2-fluoro-3-methoxy)phenyl]methyl-2-amino-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 257).
The present compound 257
1H-NMR (CDCl3) δ: 3.90 (3H, s), 4.65 (2H, d, J=5.8 Hz), 6.13 (2H, br s), 6.36 (1H, br s), 6.93-6.96 (2H, m), 7.07 (1H, t, J=7.1 Hz), 7.37 (1H, dd, J=8.0, 2.9 Hz), 8.06 (1H, d, J=2.9 Hz).
0.27 g of 2-amino-3-cyano-5-fluoropyridine and 2 ml of concentrated sulfuric acid were added to 4 ml of water, and the obtained mixture was heated to reflux for 7 hours 30 minutes. Thereafter, aqueous ammonia was added to the reaction mixture, so that the pH was adjusted to pH 10. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-5-fluoronicotinic acid.
The thus obtained crude 2-amino-5-fluoronicotinic acid, 0.49 g of 5-phenoxythiophen-2-yl-methylamine and 0.73 ml of triethylamine were added to 5 ml of DMF. Thereafter, 1.05 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, so as to obtain 0.61 g of N-(5-phenoxythiophen-2-yl)methyl-2-amino-5-fluoronicotinic acid amide (hereinafter referred to as the present compound 258).
The present compound 258
1H-NMR (CDCl3) δ: 4.65 (2H, d, J=5.6 Hz), 6.15 (2H, br s), 6.27 (1H, br s), 6.40 (1H, d, J=3.9 Hz), 6.75 (1H, d, J=3.9 Hz), 7.09-7.14 (3H, m), 7.31-7.38 (3H, m), 8.08 (1H, d, J=2.9 Hz).
0.46 g of 2-chloro-3-carboxyl-6-methoxymethylpyridine and 5 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 6 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-methoxymethylnicotinic acid.
The thus obtained crude 2-amino-6-methoxymethylnicotinic acid 0.57 g of 4-benzyloxybenzylamine hydrochloride, and 0.84 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.21 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 9 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, and it was then subjected to silica gel column chromatography, so as to obtain 0.22 g of N-[(4-benzyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 259).
The present compound 259
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.52 (2H, d, J=5.6 Hz), 5.07 (2H, s), 6.22 (1H, br s), 6.42 (2H, br s), 6.68 (1H, d, J=8.0 Hz), 6.95-6.98 (2H, m), 7.25-7.44 (5H, m), 7.26-7.27 (2H, m), 7.58 (1H, d, J=8.0 Hz).
0.24 g of 2-chloro-3-carboxyl-6-methoxymethylpyridine and 4 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 10 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-methoxymethylnicotinic acid.
The thus obtained crude 2-amino-6-methoxymethylnicotinic acid, 0.25 g of 5-phenoxythiophen-2-yl-methylamine and 0.45 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.60 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 9 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the precipitated crystal was then filtrated. The obtained crystal was washed with a mixed solvent of hexane and MTBE, and it was then subjected to silica gel column chromatography, so as to obtain 0.22 g of N-(5-phenoxythiophen-2-yl)-methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 260).
The present compound 260
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.64 (2H, d, J=5.6 Hz), 6.35-6.39 (4H, br m), 6.69-6.74 (2H, m), 7.08-7.13 (3H, m), 7.32-7.34 (2H, m), 7.61 (1H, d, J=7.7 Hz).
A mixture of 0.63 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 18 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 0.81 g of 5-phenoxythiophen-2-yl-methylamine and 1.45 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.92 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 9 hours 30 minutes. After water was added to the reaction mixture, the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.21 g of N-(5-phenoxythiophen-2-yl)-methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 261).
The present compound 261
1H-NMR (CDCl3) δ: 4.64 (2H, d, J=5.6 Hz), 6.16 (1H, dd, J=8.1, 2.9 Hz), 6.21 (1H, br s), 6.39 (1H, d, J=3.7 Hz), 6.58 (2H, br s), 6.74 (1H, t, J=2.2 Hz), 7.09-7.12 (3H, m), 7.31-7.34 (2H, m), 7.68 (1H, t, J=8.1 Hz).
A mixture of 0.31 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide, 0.91 ml of a 40% methylamine solution and 2.5 ml of N-methyl-2-pyrrolidone was subjected to a microwave reactor (production name: Discover; manufactured by CEM) at 18 kgf/cm2 at 150° C. for 10 minutes. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.16 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methylaminonicotinic acid amide (hereinafter referred to as the present compound 262).
The present compound 262
1H-NMR (CDCl3) δ: 2.90 (3H, d, J=5.1 Hz), 4.54 (2H, d, J=5.6 Hz), 4.61 (1H, br s), 5.69 (1H, d, J=8.5 Hz), 6.00 (1H, br s), 6.45 (2H, br s), 6.98-7.01 (4H, m), 7.08-7.12 (1H, m), 7.25-7.40 (5H, m).
1.0 g of N-(4-phenoxyphenyl)methyl-2-amino-6-methylnicotinic acid amide and 0.91 g of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetan-2,4-disulfide (a Lawesson's reagent) were added to 10 ml of 1,4-dioxane. The obtained mixture was heated to reflux for 8 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 197 mg of N-(4-phenoxyphenyl)methyl-2-amino-6-methyl-nicotinic acid thioamide (hereinafter referred to as the present compound 263).
The present compound 112
1H-NMR (CDCl3) δ: 2.36 (3H, s), 4.91 (2H, d, J=5.1 Hz), 5.95 (2H, br s), 6.48 (1H, d, J=7.7 Hz), 6.99-7.04 (4H, m), 7.13 (1H, td, J=7.4, 1.0 Hz), 7.31-7.38 (5H, m), 7.66 (1H, br s).
0.44 g of a BOP reagent and 0.3 ml of triethylamine were added to a mixture of 0.11 g of 2-aminonicotinic acid, 0.20 g of 3-(3-ethynylphenyloxy)benzylamine hydrochloride and 5 ml of DMF, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with a 5% sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.22 g of N-[3-(3-ethynylphenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 264).
The present compound 264
1H-NMR (CDCl3) δ: 3.07 (1H, s), 4.59 (2H, d, J=5.6 Hz), 6.33 (3H, s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.93 (1H, d, J=8.0 Hz), 6.99-7.03 (2H, m), 7.09-7.11 (2H, m), 7.23-7.35 (3H, m), 7.59 (1H, d, J=8.0 Hz), 8.17 (1H, d, J=4.9 Hz).
0.44 g of triethylamine was added to a mixture solution of 0.20 g of 2-aminonicotinic acid, 0.39 g of 3-(2-trifluoromethylphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.71 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.53 g of N-[3-(2-trifluoromethylphenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 265).
The present compound 265
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=6.1 Hz), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.91 (1H, dd, J=8.0, 2.4 Hz), 7.00-7.09 (4H, m), 7.15 (1H, d, J=7.6 Hz), 7.29-7.34 (1H, m), 7.36-7.41 (1H, m), 7.62-7.66 (1H, m), 7.78 (1H, d, J=7.6 Hz), 7.91 (1H, dd, J=7.6, 1.7 Hz), 8.08 (1H, dd, J=4.6, 1.7 Hz), 8.99 (1H, t, J=5.9 Hz).
0.25 g of 2-amino-6-methoxymethylnicotinic acid, 0.39 g of 3-phenoxybenzylamine hydrochloride, 0.70 g of triethylamine and 0.73 g of a BOP reagent were added to 10 ml of DMF. The obtained mixture was stirred at a room temperature for 16 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with water, and it was then dried over sodium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography, so as to obtain 0.08 g of N-(3-phenoxyphenyl)methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 266).
The present compound 266
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.57 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.37 (2H, br s), 6.69 (1H, d, J=7.8 Hz), 6.91-7.14 (6H, m), 7.26-7.36 (3H, m), 7.59 (1H, d, J=7.8 Hz).
0.54 g of 2-chloro-6-methoxymethylnicotinic acid and 10 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 10 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure, so as to obtain 0.52 g of crude 2-amino-6-methoxymethylnicotinic acid.
0.26 g of the above crude 2-amino-6-methoxymethylnicotinic acid, 0.34 g of 3-(2-fluorophenyloxy)benzylamine and 0.49 ml of triethylamine were added to 5 ml of DMF. Thereafter, 0.65 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.32 g of N-[3-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 267).
The present compound 267
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.57 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.38 (2H, br s), 6.70 (1H, d, J=7.7 Hz), 6.87-6.89 (1H, m), 6.96 (1H, s), 7.05-7.19 (5H, m), 7.26-7.32 (1H, m), 7.60 (1H, d, J=7.7 Hz).
0.26 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 246, 0.34 g of 3-(3-fluorophenyloxy)benzylamine and 0.49 ml of triethylamine were added to 5 ml of DMF. Thereafter, 0.65 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.36 g of N-[3-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 268).
The present compound 268
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.58 (2H, d, J=5.6 Hz), 6.39 (3H, br s), 6.68-6.72 (2H, m), 6.77-6.81 (2H, m), 6.95 (1H, dd, J=8.0, 2.2 Hz), 7.01 (1H, s), 7.12 (1H, d, J=7.7 Hz), 7.28-7.32 (2H, m), 7.61 (1H, d, J=7.7 Hz).
5.94 g of 2-chloro-6-methoxymethylnicotinic acid and 60 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 10 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure, so as to obtain 4.00 g of crude 2-amino-6-methoxymethylnicotinic acid.
0.40 g of the above crude 2-amino-6-methoxymethylnicotinic acid, 0.58 g of 3-(4-fluorophenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.21 g of N-[3-(4-fluorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 269).
The present compound 269
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.57 (2H, d, J=5.6 Hz), 6.29 (1H, s), 6.38 (2H, br s), 6.70 (1H, d, J=7.8 Hz), 6.87 (1H, t, J=5.4 Hz), 6.95-7.07 (6H, m), 7.26-7.32 (1H, m), 7.60 (1H, d, J=7.8 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.61 g of 3-(4-trifluoromethylphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.09 g of N-[3-(4-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 270).
The present compound 270
1H-NMR (CDCl3) δ: 3.42 (3H, s), 4.35 (2H, s), 4.55 (2H, d, J=5.9 Hz), 6.64 (1H, d, J=7.8 Hz), 6.73 (2H, br s), 6.94 (1H, d, J=8.0 Hz), 7.02-7.04 (3H, m), 7.13 (1H, d, J=7.6 Hz), 7.34 (1H, t, J=7.9 Hz), 7.54-7.57 (3H, m), 7.63 (1H, d, J=7.8 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.64 g of 3-(3-trifluoromethoxyphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.14 g of N-[3-(3-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 271).
The present compound 271
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.39 (2H, s), 4.59 (2H, d, J=5.8 Hz), 6.35-6.39 (3H, br m), 6.70 (1H, d, J=8.0 Hz), 6.91-6.97 (4H, m), 7.13 (1H, d, J=7.7 Hz), 7.34 (3H, m), 7.61 (1H, d, J=8.0 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.64 g of 3-(4-trifluoromethoxyphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.29 g of N-[3-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 272).
The present compound 272
1H-NMR (CDCl3) δ: 3.41 (3H, s), 4.35 (2H, s), 4.54 (2H, d, J=5.8 Hz), 6.36 (1H, br s), 6.65 (1H, d, J=7.7 Hz), 6.93-6.97 (2H, m), 7.08-7.18 (6H, m), 7.26-7.34 (2H, m), 7.61 (1H, d, J=7.7 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.64 g of 3-(4-chlorophenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.25 g of N-[3-(4-chlorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 273).
The present compound 273
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.39 (2H, s), 4.56 (2H, d, J=5.7 Hz), 6.34-6.37 (3H, br m), 6.70 (1H, m), 6.87-7.11 (6H, m), 7.27-7.32 (2H, m), 7.60-7.61 (1H, m).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.64 g of 3-(2-trifluoromethylphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 10 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.10 g of N-[3-(2-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 274).
The present compound 274
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.59 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.38 (2H, br s), 6.71 (1H, d, J=7.8 Hz), 6.95-7.01 (3H, m), 7.12-7.36 (3H, m), 7.45-7.47 (1H, m), 7.61 (1H, d, J=6.8 Hz), 7.68 (1H, d, J=7.8 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.48 g of 3-(4-methylphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.13 g of N-[3-(4-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 275).
The present compound 275
1H-NMR (CDCl3) δ: 2.34 (3H, s), 3.46 (3H, s), 4.40 (2H, s), 4.56 (2H, d, J=4.6 Hz), 6.28 (1H, br s), 6.37 (2H, br s), 6.69 (1H, d, J=7.2 Hz), 6.99-7.18 (8H, m), 7.59 (1H, d, J=7.2 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.48 g of 3-(2-methoxyphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 12 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.08 g of N-[3-(2-methoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 276).
The present compound 276
1H-NMR (CDCl3) δ: 3.45 (3H, s), 3.81 (3H, s), 4.39 (2H, s), 4.54 (2H, d, J=5.4 Hz), 6.38 (3H, br s), 6.67 (1H, d, J=7.8 Hz), 6.82 (1H, d, J=7.6 Hz), 6.97 (5H, m), 7.13-7.26 (2H, m), 7.59 (1H, d, J=7.8 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.48 g of 3-(2-methylphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 9 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.13 g of N-[3-(2-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 277).
The present compound 277
1H-NMR (CDCl3) δ: 2.23 (3H, s), 3.46 (3H, s), 4.40 (2H, s), 4.56 (2H, d, J=5.8 Hz), 6.33-6.38 (4H, br m), 6.83-7.15 (8H, m), 7.60 (1H, d, J=8.0 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.52 g of 3-(3-methoxyphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.10 g of N-[3-(3-methoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 278).
The present compound 278
1H-NMR (CDCl3) δ: 3.45 (3H, s), 3.78 (3H, s), 4.39 (2H, s), 4.56 (2H, d, J=5.6 Hz), 6.47 (2H, br s), 6.57-6.59 (2H, m), 6.65-6.68 (2H, m), 6.91-7.09 (4H, m), 7.15-7.35 (2H, m), 7.72 (1H, d, J=7.7 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.52 g of 3-(3-methoxyphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[3-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 279).
The present compound 279
1H-NMR (CDCl3) δ: 3.46 (3H, s), 3.78 (3H, s), 4.40 (2H, s), 4.58 (2H, d, J=5.8 Hz), 6.29 (1H, br s), 6.41 (2H, br s), 6.59 (2H, m), 6.66-6.71 (2H, m), 6.94-7.09 (3H, m), 7.21-7.29 (2H, m), 7.61 (1H, d, J=8.0 Hz).
0.40 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the intermediate of Production example 248, 0.48 g of 3-(3-methylphenyloxy)benzylamine and 0.83 ml of triethylamine were added to 6 ml of DMF. Thereafter, 1.10 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[3-(3-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 280).
The present compound 280
1H-NMR (CDCl3) δ: 2.33 (3H, s), 3.46 (3H, s), 4.39 (2H, s), 4.57 (2H, d, J=5.8 Hz), 6.28 (1H, br s), 6.39 (2H, br s), 6.70 (1H, d, J=8.0 Hz), 6.81-6.82 (2H, m), 6.92-6.96 (3H, m), 7.05-7.07 (1H, m), 7.23-7.29 (2H, m), 7.60 (1H, d, J=8.0 Hz).
0.23 g of 2-amino-6-methoxymethylnicotinic acid, 0.28 g of 3-(3-trifluoromethylphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.05 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.28 g of N-[3-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 281).
The present compound 281
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.60 (2H, d, J=5.8 Hz), 6.33-6.36 (3H, br m), 6.70 (1H, d, J=8.0 Hz), 6.95 (1H, t, J=3.9 Hz), 7.02 (1H, s), 7.16 (2H, t, J=9.7 Hz), 7.31-7.40 (4H, m), 7.61 (1H, d, J=8.0 Hz).
A mixture of 0.64 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 11 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 0.94 g of 3-pheoxybenzylamine hydrochloride and 1.47 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.95 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 6 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.14 g of N-(3-phenoxy)phenylmethyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 282).
The present compound 282
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.8 Hz), 6.15 (1H, dd, J=8.3, 2.8 Hz), 6.20 (1H, br s), 6.58 (2H, br s), 6.91-7.14 (6H, m), 7.29-7.36 (3H, m), 7.68 (1H, t, J=8.1 Hz).
A mixture of 0.63 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 12 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 1.01 g of 3-(2-fluorophenyloxy)benzylamine hydrochloride and 1.46 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.94 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.26 g of N-[3-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 283).
The present compound 283
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.4 Hz), 6.15-6.17 (2H, m), 6.59 (2H, br s), 6.88 (1H, d, J=8.5 Hz), 6.96 (1H, s), 7.04-7.32 (6H, m), 7.68 (1H, t, J=7.7 Hz).
A mixture of 0.62 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 9 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 0.99 g of 3-(4-fluorophenyloxy)benzylamine hydrochloride and 1.43 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.89 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 12 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[3-(4-fluorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 284).
The present compound 284
1H-NMR (CDCl3) δ: 4.56 (2H, d, J=5.9 Hz), 6.15 (1H, dd, J=8.0, 2.7 Hz), 6.19 (1H, br s), 6.59 (2H, br s), 6.87-7.06 (7H, m), 7.27-7.31 (1H, m), 7.69 (1H, t, J=8.0 Hz).
A mixture of 0.61 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 7 hours 30 minutes. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 0.97 g of 3-(3-fluorophenyloxy)benzylamine hydrochloride and 1.41 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.87 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 9 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.12 g of N-[3-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 285).
The present compound 285
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.8 Hz), 6.16 (1H, dd, J=8.2, 2.7 Hz), 6.22 (1H, br s), 6.60 (2H, br s), 6.70 (1H, m), 6.80 (2H, m), 6.98 (3H, m), 7.12 (2H, m), 7.29-7.34 (1H, m), 7.69 (1H, t, J=8.2 Hz).
A mixture of 0.62 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 14 hours 30 minutes. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 0.83 g of 3-(4-methylphenyloxy)benzylamine and 1.42 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.89 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 1 hour 30 minutes. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.12 g of N-[3-(4-methylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 286).
The present compound 286
1H-NMR (CDCl3) δ: 2.34 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.15 (1H, dd, J=8.2, 2.9 Hz), 6.18 (1H, br s), 6.58 (2H, br s), 6.88-6.94 (4H, m), 7.03 (1H, d, J=7.5 Hz), 7.14 (2H, d, J=8.7 Hz), 7.26-7.31 (1H, m), 7.67 (1H, t, J=8.2 Hz).
A mixture of 0.61 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 16 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The thus obtained crude 2-amino-6-fluoronicotinic acid, 1.03 g of 3-(3-trifluoromethylphenyloxy)benzylamine and 1.41 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.87 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.17 g of N-[3-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 287).
The present compound 287
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.8 Hz), 6.16 (1H, dd, J=8.5, 2.7 Hz), 6.21 (1H, br s), 6.59 (2H, br s), 6.95-7.00 (2H, m), 7.14-7.18 (2H, m), 7.24-7.26 (1H, m), 7.35-7.38 (2H, m), 7.44-7.46 (1H, m), 7.69 (1H, t, J=8.5 Hz).
0.18 g of 2-amino-6-fluoronicotinic acid, 0.25 g of 3-(3-methoxyphenyloxy)benzylamine and 0.40 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.53 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.25 g of N-[3-(3-methoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 288).
The present compound 288
1H-NMR (CDCl3) δ: 3.78 (3H, s), 4.57 (2H, d, J=5.6 Hz), 6.14-6.16 (2H, m), 6.60-6.65 (4H, m), 6.95-6.98 (2H, m), 7.07 (1H, d, J=7.7 Hz), 7.25-7.30 (3H, m), 7.68 (1H, t, J=8.0 Hz).
0.16 g of 2-amino-6-fluoronicotinic acid, 0.28 g of 3-(4-trifluoromethoxyphenyloxy)benzylamine and 0.36 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.48 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.27 g of N-[3-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 289).
The present compound 289
1H-NMR (CDCl3) δ: 4.59 (2H, d, J=5.6 Hz), 6.16 (1H, dd, J=8.3, 2.8 Hz), 6.22 (1H,br s), 6.59 (2H,br s), 6.93 (1H, m), 7.01 (3H, m), 7.10 (1H, d, J=7.5 Hz), 7.19 (2H, d, J=9.2 Hz), 7.34 (1H, m), 7.69 (1H, t, J=8.3 Hz).
0.15 g of 2-amino-6-fluoronicotinic acid, 0.26 g of 3-(3-trifluoromethoxyphenyloxy)benzylamine and 0.34 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.45 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.27 g of N-[3-(3-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 290).
The present compound 290
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.9 Hz), 6.15 (1H, dd, J=8.3, 2.7 Hz), 6.24 (1H, br s), 6.60 (2H, br s), 6.85-7.01 (5H, m), 7.12-7.14 (1H, m), 7.33-7.35 (2H, m), 7.69 (1H, t, J=8.3 Hz).
0.16 g of 2-amino-6-fluoronicotinic acid, 0.22 g of 3-(4-methoxyphenyloxy)benzylamine and 0.36 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.47 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 30° C. for 16 hours 30 minutes. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.26 g of N-[3-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 291).
The present compound 291
1H-NMR (CDCl3) δ: 3.80 (3H, s), 4.58 (2H, d, J=5.9 Hz), 6.15 (1H, dd, J=8.3, 2.7 Hz), 6.24 (1H, br s), 6.60 (2H, br s), 6.85-7.01 (5H, m), 7.12-7.14 (1H, m), 7.33-7.35 (2H, m), 7.69 (1H, t, J=8.0 Hz).
0.17 g of 2-amino-6-fluoronicotinic acid, 0.28 g of 3-(2-trifluoromethylphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.31 g of N-[3-(2-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 292).
The present compound 292
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=5.3 Hz), 6.16 (1H, d, J=7.5 Hz), 6.23 (1H, br s), 6.59 (2H, br s), 6.96-7.00 (3H, m), 7.18-7.29 (3H, m), 7.45-7.47 (1H, m), 7.68-7.71 (2H, m).
0.17 g of 2-amino-6-fluoronicotinic acid, 0.24 g of 3-(2-methoxyphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 7 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.30 g of N-[3-(2-methoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 293).
The present compound 292
1H-NMR (CDCl3) δ: 3.83 (3H, s), 4.55 (2H, d, J=5.6 Hz), 6.14-6.16 (2H, m), 6.58 (2H, br s), 6.83 (1H, dd, J=8.2, 2.4 Hz), 6.92-6.94 (2H, m), 6.99-7.01 (3H, m), 7.14-7.18 (1H, m), 7.23-7.29 (1H, m), 7.67 (1H, t, J=8.2 Hz).
0.17 g of 2-amino-6-fluoronicotinic acid, 0.22 g of 3-(3-methylphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 7 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.25 g of N-[3-(3-methylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 294).
The present compound 294
1H-NMR (CDCl3) δ: 2.33 (3H, s), 4.56 (2H, d, J=5.6 Hz), 6.15 (1H, dd, J=8.3, 2.5 Hz), 6.18 (1H, br s), 6.59 (2H, br s), 6.81-6.82 (2H, m), 6.92-6.98 (3H, m), 7.05 (1H, d, J=7.7 Hz), 7.23-7.30 (2H, m), 7.68 (1H, t, J=8.3 Hz).
0.17 g of 2-amino-6-fluoronicotinic acid, 0.24 g of 3-(4-chlorophenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 8 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.17 g of N-[3-(4-chlorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 295).
The present compound 295
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.8 Hz), 6.16 (1H, dd, J=8.0, 2.7 Hz), 6.20 (1H, br s), 6.59 (2H, br s), 6.90-6.97 (4H, m), 7.08 (1H, d, J=7.2 Hz), 7.28-7.33 (3H, m), 7.68 (1H, t, J=8.0 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.33 g of 3-(2-fluorophenyloxy)benzylamine hydroxide and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.36 g of N-[3-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 296).
The present compound 296
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.40 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.8 Hz), 6.81 (1H, d, J=8.0 Hz), 6.92 (1H, s), 7.03-7.08 (3H, m), 7.17-7.25 (3H, m), 7.30-7.42 (2H, m), 7.82 (1H, d, J=7.8 Hz), 8.87 (1H, t, J=5.7 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.33 g of 3-(3-fluorophenyloxy)benzylamine hydroxide and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.34 g of N-[3-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 297).
The present compound 297
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.43 (2H, d, J=5.9 Hz), 6.46 (1H, d, J=7.8 Hz), 6.80-6.88 (2H, m), 6.91-7.16 (6H, m), 7.35-7.43 (2H, m), 7.85 (1H, d, J=7.8 Hz), 8.89 (1H, t, J=5.0 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.33 g of 3-(4-fluorophenyloxy)benzylamine hydroxide and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.37 g of N-[3-(4-fluorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 298).
The present compound 298
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.40 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.84 (1H, d, J=8.0 Hz), 6.92 (1H, s), 7.03-7.09 (5H, m), 7.19-7.25 (2H, m), 7.30-7.35 (1H, m), 7.83 (1H, d, J=7.8 Hz), 8.87 (1H, t, J=5.9 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.31 g of 3-(2-chlorophenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.41 g of N-[3-(2-chlorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 299).
The present compound 299
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.40 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.79 (1H, dd, J=8.3, 2.2 Hz), 6.91 (1H, s), 7.02-7.11 (4H, m), 7.19-7.25 (1H, m), 7.30-7.38 (2H, m), 7.59 (1H, d, J=8.0 Hz), 7.82 (1H, d, J=7.8 Hz), 8.87 (1H, t, J=6.0 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.31 g of 3-(4-chlorophenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. Ethyl acetate and hexane were added to the obtained residue, and the precipitated solid was then collected, so as to obtain 0.33 g of N-[3-(4-chlorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 300).
The present compound 300
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.41 (2H, d, J=5.8 Hz), 6.45 (1H, d, J=7.7 Hz), 6.88-7.15 (7H, m), 7.33-7.38 (1H, m), 7.42 (2H, d, J=8.5 Hz), 7.84 (1H, d, J=7.7 Hz), 8.88 (1H, t, J=5.8 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.28 g of 3-(2-methylphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.36 g of N-[3-(2-methylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 301).
The present compound 301
1H-NMR (DMSO-D6) δ: 2.15 (3H, s), 2.27 (3H, s), 4.38 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.7 Hz), 6.72 (1H, d, J=7.2 Hz), 6.84 (1H, s), 6.89 (1H, d, J=8.0 Hz), 6.99-7.13 (4H, m), 7.18-7.23 (1H, m), 7.25-7.34 (2H, m), 7.81 (1H, d, J=7.7 Hz), 8.86 (1H, t, J=5.6 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.28 g of 3-(4-methylphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.38 g of N-[3-(4-methylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 302234).
The present compound 302
1H-NMR (DMSO-D6) δ: 2.28 (6H, s), 4.39 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.82 (1H, d, J=8.0 Hz), 6.89-6.93 (3H, m), 7.02-7.08 (3H, m), 7.18 (2H, d, J=8.3 Hz), 7.27-7.34 (1H, m), 7.82 (1H, d, J=7.8 Hz), 8.86 (1H, t, J=5.6 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.35 g of 3-(2-trifluoromethylphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.42 g of N-[3-(2-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 303).
The present compound 303
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.43 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.91 (1H, d, J=8.0 Hz), 6.98-7.09 (4H, m), 7.14 (1H, d, J=7.3 Hz), 7.29-7.41 (2H, m), 7.60-7.68 (1H, m), 7.78 (1H, d, J=7.6 Hz), 7.83 (1H, d, J=7.8 Hz), 8.88 (1H, t, J=5.6 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.35 g of 3-(3-trifluoromethylphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.43 g of N-[3-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 304).
The present compound 304
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.43 (2H, d, J=5.4 Hz), 6.45 (1H, d, J=7.6 Hz), 6.97 (1H, d, J=8.3 Hz), 7.02-7.09 (3H, m), 7.16 (1H, d, J=7.6 Hz), 7.26-7.32 (2H, m), 7.37-7.43 (1H, m), 7.49 (1H, d, J=7.3 Hz), 7.59-7.65 (1H, m), 7.84 (1H, d, J=7.6 Hz), 8.89 (1H, s).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.35 g of 3-(4-trifluoromethylphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.43 g of N-[3-(4-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 305).
The present compound 305
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.44 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.8 Hz), 7.00 (1H, d, J=8.3 Hz), 7.04-7.07 (3H, m), 7.14 (2H, d, J=8.5 Hz), 7.18 (1H, d, J=7.6 Hz), 7.39-7.43 (1H, m), 7.73 (2H, d, J=8.5 Hz), 7.84 (1H, d, J=7.8 Hz), 8.89 (1H, t, J=5.4 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.30 g of 3-(2-methoxyphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.39 g of N-[3-(2-methoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 306).
The present compound 306
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 3.71 (3H, s), 4.36 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=7.8 Hz), 6.63-6.66 (1H, m), 6.79 (1H, s), 6.94-6.98 (2H, m), 7.00-7.06 (3H, m), 7.13-7.26 (3H, m), 7.81 (1H, d, J=7.8 Hz), 8.85 (1H, t, J=5.7 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.30 g of 3-(3-methoxyphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.34 g of N-[3-(3-methoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 307).
The present compound 307
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 3.72 (3H, s), 4.41 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.8 Hz), 6.51-6.58 (2H, m), 6.71 (1H, d, J=8.0 Hz), 6.88 (1H, d, J=7.8 Hz), 6.96 (1H, s), 7.02-7.11 (3H, m), 7.24-7.30 (1H, m), 7.31-7.37 (1H, m), 7.83 (1H, d, J=7.8 Hz), 8.88 (1H, t, J=5.4 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.37 g of 3-(3-trifluoromethoxyphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.42 g of N-[3-(3-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 308).
The present compound 308
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.43 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.8 Hz), 6.94-7.17 (8H, m), 7.36-7.41 (1H, m), 7.47-7.53 (1H, m), 7.84 (1H, d, J=7.8 Hz), 8.89 (1H, t, J=5.6 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.37 g of 3-(4-trifluoromethoxyphenyloxy)benzylamine and 5 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 24 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was successively washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.43 g of N-[3-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 309).
The present compound 309
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.42 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.8 Hz), 6.92 (1H, d, J=8.0 Hz), 7.00 (1H, s), 7.03-7.15 (5H, m), 7.33-7.42 (3H, m), 7.84 (1H, d, J=7.8 Hz), 8.88 (1H, t, J=5.4 Hz).
0.60 g of 4-fluorobenzonitrile, 0.30 g of N-(4-hydroxyphenylmethyl)-2-aminonicotinic acid amide and 0.60 g of cesium carbonate were added to 8 ml of DMF, and the mixture was then heated to reflux for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.10 g of N-[4-(4-cyanophenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 310).
The present compound 310
1H-NMR (CDCl3) δ: 4.62 (2H, d, J=5.9 Hz), 6.37 (3H, br s), 6.60 (1H, dd, J=7.6, 4.9 Hz), 7.01-7.06 (4H, m), 7.38-7.40 (2H, m), 7.59-7.62 (3H, m), 8.18 (1H, dd, J=4.9, 1.7 Hz).
1.0 g of 2-fluorobenzonitrile, 0.50 g of N-(4-hydroxyphenylmethyl)-2-aminonicotinic acid amide and 1.0 g of cesium carbonate were added to 10 ml of DMF, and the mixture was then stirred at a room temperature for 4 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.47 g of N-[4-(2-cyanophenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 311).
The present compound 311
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.6 Hz), 6.38 (2H, br s), 6.46 (1H, br s), 6.59 (1H, dd, J=7.6, 4.9 Hz), 6.88 (1H, d, J=8.5 Hz), 7.04-7.06 (2H, m), 7.14-7.16 (1H, m), 7.36-7.37 (2H, m), 7.46-7.49 (1H, m), 7.64-7.66 (2H, m), 8.16 (1H, dd, J=4.9, 1.7 Hz).
1.0 g of 3-fluorobenzonitrile, 0.50 g of N-(4-hydroxyphenylmethyl)-2-aminonicotinic acid amide and 1.0 g of cesium carbonate were added to 10 ml of DMF, and the mixture was then stirred at a room temperature for 4 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.41 g of N-[4-(3-cyanophenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 312).
The present compound 312
1H-NMR (CDCl3) δ: 4.61 (2H, d, J=5.6 Hz), 6.38 (3H, br s), 6.59 (1H, dd, J=7.8, 4.8 Hz), 7.01-7.03 (2H, m), 7.21-7.24 (3H, m), 7.35-7.44 (3H, m), 7.63 (1H, dd, J=7.8, 1.8 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.36 g of 4-(2-chloro-4-trifluoromethylphenyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.21 g of N-[4-(2-chloro-4-trifluoromethylphenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 313).
The present compound 313
1H-NMR (CDCl3) δ: 4.60 (2H, d, J=5.8 Hz), 6.37 (3H, br s), 6.59 (1H, dd, J=7.6, 4.8 Hz), 6.98-7.03 (3H, m), 7.35-7.37 (3H, m), 7.57-7.61 (2H, m), 8.17 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.26 g of 4-(3-bromophenyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.11 g of N-[4-(3-bromophenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 314).
The present compound 314
1H-NMR (CDCl3) δ: 4.58 (2H, d, J=6.3 Hz), 6.35-6.38 (3H, br m), 6.57-6.61 (1H, m), 6.95-7.02 (3H, m), 7.10-7.13 (1H, m), 7.31-7.35 (4H, m), 7.59-7.62 (1H, m), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.20 g of 4-(2-bromophenyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.17 g of N-[4-(2-bromophenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 315).
The present compound 315
1H-NMR (CDCl3) δ: 4.57 (2H, d, J=5.6 Hz), 6.31-6.37 (3H, br m), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.98-7.02 (3H, m), 7.11 (1H, t, J=7.5 Hz), 7.29-7.36 (4H, m), 7.60 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.39 g of 4-(4-pentylphenyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.19 g of N-[4-(4-pentylphenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 316).
The present compound 316
1H-NMR (CDCl3) δ: 0.90 (3H, t, J=6.9 Hz), 1.32-1.33 (4H, m), 1.60-1.66 (2H, m), 2.58 (2H, t, J=7.8 Hz), 4.56 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.36 (2H, br s), 6.58 (1H, dd, J=7.8, 4.8 Hz), 6.92-6.97 (4H, m), 7.14 (2H, d, J=8.6 Hz), 7.27-7.29 (2H, m), 7.59 (1H, dd, J=7.8, 1.8 Hz), 8.16 (1H, dd, J=4.8, 1.8 Hz).
A mixture of 0.25 g of 2-aminonicotinic acid, 0.20 g of 1-hydroxybenzotriazole, 0.43 g of WSC, 0.39 g of 4-(4-chloro-3,5-dimethylphenyloxy)benzylamine and 2 ml of DMF was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with ethyl acetate twice. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.28 g of N-[4-(4-chloro-3,5-dimethylphenyloxy)phenyl]methyl-2-aminonicotinic acid amide (hereinafter referred to as the present compound 317).
The present compound 317
1H-NMR (CDCl3) δ: 2.34 (6H, s), 4.58 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.37 (2H, br s), 6.59 (1H, dd, J=7.6, 4.8 Hz), 6.74 (2H, s), 6.97 (2H, d, J=8.6 Hz), 7.29-7.32 (2H, m), 7.60 (1H, dd, J=7.6, 1.6 Hz), 8.17 (1H, dd, J=4.8, 1.8 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.33 g of 4-(2-fluorophenyloxy)benzylamine hydroxide and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.36 g of N-[4-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 318).
The present compound 318
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.39 (2H, d, J=5.9 Hz), 6.45 (1H, d, J=8.0 Hz), 6.94 (2H, d, J=8.5 Hz), 7.08 (2H, s), 7.10-7.17 (1H, m), 7.18-7.27 (2H, m), 7.31 (2H, d, J=8.5 Hz), 7.34-7.41 (1H, m), 7.87 (1H, d, J=7.8 Hz), 8.86 (1H, t, J=5.4 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.29 g of 4-(3-fluorophenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 6 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.40 g of N-[4-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 319).
The present compound 319
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.42 (2H, d, J=5.9 Hz), 6.46 (1H, d, J=7.8 Hz), 6.77-6.85 (2H, m), 6.92-6.97 (1H, m), 7.04 (2H, d, J=8.3 Hz), 7.09 (2H, s), 7.36 (2H, d, J=8.3 Hz), 7.38-7.42 (1H, m), 7.88 (1H, d, J=7.8 Hz), 8.89 (1H, t, J=5.7 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.35 g of 4-(3-trifluoromethylphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.37 g of N-[4-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 320).
The present compound 320
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.44 (2H, d, J=5.6 Hz), 6.46 (1H, d, J=8.0 Hz), 7.05-7.13 (4H, m), 7.27 (2H, s), 7.38 (2H, d, J=8.2 Hz), 7.47 (1H, d, J=7.5 Hz), 7.58-7.63 (1H, m), 7.88 (1H, d, J=8.0 Hz), 8.90 (1H, t, J=5.4 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.30 g of 4-(4-methoxyphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.32 g of N-[4-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 321).
The present compound 321
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 3.74 (3H, s), 4.38 (2H, d, J=5.6 Hz), 6.45 (1H, d, J=7.7 Hz), 6.88 (2H, d, J=8.2 Hz), 6.92-7.00 (4H, m), 7.08 (2H, s), 7.28 (2H, d, J=8.2 Hz), 7.86 (1H, d, J=7.7 Hz), 8.85 (1H, t, J=5.3 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.37 g of 4-(3-trifluoromethoxyphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction mixture, and the precipitated solid was then collected by filtration. The obtained solid was washed with a saturated sodium bicarbonate aqueous solution, water and a mixed solution of MTBE and hexane, and it was then dried, so as to obtain 0.45 g of N-[4-(3-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 322).
The present compound 322
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.43 (2H, d, J=5.8 Hz), 6.46 (1H, d, J=7.7 Hz), 6.95-6.99 (2H, m), 7.04-7.13 (5H, m), 7.37 (2H, d, J=8.2 Hz), 7.46-7.51 (1H, m), 7.88 (1H, d, J=7.7 Hz), 8.89 (1H, t, J=5.6 Hz).
0.40 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-methylnicotinic acid, 0.42 g of 4-(4-trifluoromethoxyphenyloxy)benzylamine hydrochloride and 3 ml of DMF. Thereafter, 0.64 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The precipitated solid was dried, so as to obtain 0.38 g of N-[4-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methylnicotinic acid amide (hereinafter referred to as the present compound 323).
The present compound 323
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.42 (2H, d, J=5.8 Hz), 6.46 (1H, d, J=7.7 Hz), 7.02-7.14 (6H, m), 7.33-7.43 (4H, m), 7.88 (1H, d, J=7.7 Hz), 8.89 (1H, t, J=5.6 Hz).
3.00 g of 2-chloro-6-methoxymethylnicotinic acid and 45 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred at 180° C. under pressure for 18 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure, so as to obtain 0.52 g of crude 2-amino-6-methoxymethylnicotinic acid.
0.23 g of the above crude 2-amino-6-methoxymethylnicotinic acid, 0.23 g of 4-(3-fluorophenyloxy)benzylamine and 0.39 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.51 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.26 g of N-[4-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 324).
The present compound 324
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.59 (2H, d, J=5.6 Hz), 6.28 (1H, br s), 6.41 (2H, br s), 6.72-6.77 (4H, m), 7.02 (2H, d, J=8.2 Hz), 7.27-7.33 (3H, m), 7.62 (1H, d, J=7.7 Hz).
0.23 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.30 g of 4-(3-trifluoromethoxyphenyloxy)benzylamine and 0.39 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.51 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.33 g of N-[4-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 325).
The present compound 325
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.60 (2H, d, J=5.6 Hz), 6.30 (1H, br s), 6.41 (2H, br s), 6.71 (1H, d, J=8.0 Hz), 6.84-6.87 (2H, m), 6.91-6.96 (2H, m), 7.03 (2H, d, J=8.5 Hz), 7.31-7.36 (2H, m), 7.63 (1H, d, J=8.0 Hz).
0.22 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.33 g of 4-(4-trifluoromethoxyphenyloxy)benzylamine and 0.37 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.34 g of N-[4-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 326).
The present compound 326
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.58 (2H, d, J=5.8 Hz), 6.71 (1H, d, J=8.0 Hz), 7.00-7.01 (4H, m), 7.18 (2H, d, J=9.2 Hz), 7.33 (2H, d, J=8.2 Hz), 7.62 (1H, d, J=8.0 Hz).
0.23 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.26 g of 4-(2-fluorophenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 5 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.30 g of N-[4-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 327).
The present compound 327
1H-NMR (CDCl3) δ: 3.45 (3H, s), 4.40 (2H, s), 4.56 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.40 (2H, br s), 6.70 (1H, d, J=8.0 Hz), 6.96 (2H, d, J=8.7 Hz), 7.05-7.21 (3H, m), 7.27-7.30 (3H, m), 7.60 (1H, d, J=8.0 Hz).
0.23 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.28 g of 4-(3-trifluoromethylphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.51 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 0° C. for 1 hour 30 minutes. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.29 g of N-[4-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 328).
The present compound 328
1H-NMR (CDCl3) δ: 3.46 (3H, s), 4.40 (2H, s), 4.60 (2H, d, J=5.6 Hz), 6.31 (1H, br s), 6.41 (2H, br s), 6.71 (1H, d, J=7.7 Hz), 7.02 (2H, d, J=7.5 Hz), 7.17 (1H, d, J=8.0 Hz), 7.24-7.26 (1H, m), 7.31-7.36 (3H, m), 7.44 (1H, t, J=7.6 Hz), 7.63 (1H, d, J=8.0 Hz).
0.24 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.25 g of 4-(3-methoxyphenyloxy)benzylamine and 0.40 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.53 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 45 minutes. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.10 g of N-[4-(3-methoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 329).
The present compound 329
1H-NMR (CDCl3) δ: 3.46 (3H, s), 3.78 (3H, s), 4.40 (2H, s), 4.57 (2H, d, J=5.3 Hz), 6.27 (1H, s), 6.40 (2H, br s), 6.58 (2H, d, J=7.0 Hz), 6.65-6.71 (2H, m), 7.00-7.02 (2H, m), 7.21-7.32 (3H, m), 7.61 (1H, d, J=7.7 Hz).
0.23 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.25 g of 4-(4-methoxyphenyloxy)benzylamine and 0.39 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.52 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 45 minutes. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.33 g of N-[4-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 330).
The present compound 330
1H-NMR (CDCl3) δ: 3.45 (3H, s), 3.81 (3H, s), 4.40 (2H, d, J=5.8 Hz), 4.55 (2H, d, J=5.6 Hz), 6.23 (1H, br s), 6.40 (2H, br s), 6.69 (1H, d, J=8.0 Hz), 6.87-6.99 (7H, m), 7.27-7.28 (1H, m), 7.59 (1H, d, J=8.0 Hz).
0.22 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.22 g of 4-(2-methylphenyloxy)benzylamine and 0.37 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.49 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.29 g of N-[4-(2-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 331).
The present compound 331
1H-NMR (CDCl3) δ: 2.23 (3H, s), 3.45 (3H, s), 4.39 (2H, s), 4.55 (2H, d, J=5.6 Hz), 6.25 (1H, br s), 6.40 (2H, br s), 6.69 (1H, d, J=8.0 Hz), 6.88-6.91 (3H, m), 7.08 (1H, t, J=7.1 Hz), 7.17 (1H, t, J=7.6 Hz), 7.26-7.27 (3H, m), 7.60 (1H, d, J=8.0 Hz).
0.23 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.22 g of 4-(3-methylphenyloxy)benzylamine and 0.38 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.50 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.27 g of N-[4-(3-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 332).
The present compound 332
1H-NMR (CDCl3) δ: 2.33 (3H, s), 3.46 (3H, s), 4.39 (2H, s), 4.57 (2H, d, J=5.8 Hz), 6.28 (1H, br s), 6.39 (2H, br s), 6.70 (1H, d, J=8.0 Hz), 6.81-6.82 (2H, m), 6.92-6.96 (3H, m), 7.05-7.07 (1H, m), 7.23-7.29 (2H, m), 7.60 (1H, d, J=8.0 Hz).
0.22 g of the crude 2-amino-6-methoxymethylnicotinic acid which is the production intermediate of Production example 303, 0.25 g of 4-(4-methylphenyloxy)benzylamine and 0.36 ml of triethylamine were added to 4 ml of DMF. Thereafter, 0.48 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at 40° C. for 4 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, and the precipitated solid was then filtrated. The obtained solid was washed with a mixed solution of MTBE and hexane, so as to obtain 0.29 g of N-[4-(4-methylphenyloxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 333).
The present compound 333
1H-NMR (CDCl3) δ: 2.33 (3H, s), 3.45 (3H, s), 4.39 (2H, s), 4.55 (2H, d, J=5.6 Hz), 6.43 (2H, br s), 6.69 (1H, d, J=8.0 Hz), 6.76 (1H, br s), 6.90-6.95 (4H, m), 7.14 (2H, d, J=8.0 Hz), 7.26-7.29 (2H, m), 7.68 (1H, d, J=8.0 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.33 g of 4-(2-fluorophenyloxy)benzylamine hydrochloride and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 5 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.28 g of N-[4-(2-fluorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 334).
The present compound 334
1H-NMR (DMSO-D6) δ: 4.40 (2H, d, J=5.8 Hz), 6.26 (1H, dd, J=8.3, 2.8 Hz), 6.94 (2H, d, J=8.5 Hz), 7.11-7.16 (1H, m), 7.19-7.25 (2H, m), 7.32 (2H, d, J=8.2 Hz), 7.35-7.41 (1H, m), 7.56 (2H, s), 8.12-8.18 (1H, m), 8.94 (1H, t, J=5.8 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.28 g of 4-(3-fluorophenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 5 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. Hexane and MTBE were added to the obtained residue, and the precipitated solid was collected by filtration, so as to obtain 0.30 g of N-[4-(3-fluorophenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 335).
The present compound 335
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=5.8 Hz), 6.27 (1H, dd, J=8.2, 2.4 Hz), 6.77-6.85 (2H, m), 6.93-6.98 (1H, m), 7.05 (2H, d, J=8.5 Hz), 7.34-7.43 (3H, m), 7.57 (2H, s), 8.14-8.19 (1H, m), 8.97 (1H, t, J=5.7 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.36 g of 4-(3-trifluoromethoxyphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 5 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.27 g of N-[4-(3-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 336).
The present compound 336
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=5.8 Hz), 6.27 (1H, dd, J=8.3, 2.8 Hz), 6.95-7.00 (2H, m), 7.05-7.13 (3H, m), 7.38 (2H, d, J=8.7 Hz), 7.47-7.52 (1H, m), 7.58 (2H, s), 8.15-8.19 (1H, m), 8.97 (1H, t, J=5.8 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.41 g of 4-(4-trifluoromethoxyphenyloxy)benzylamine hydrochloride and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 5 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.16 g of N-[4-(4-trifluoromethoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 337).
The present compound 337
1H-NMR (DMSO-D6) δ: 4.43 (2H, d, J=5.6 Hz), 6.27 (1H, dd, J=8.5, 2.4 Hz), 7.02-7.09 (4H, m), 7.34-7.40 (4H, m), 7.57 (2H, s), 8.14-8.19 (1H, m), 8.97 (1H, t, J=5.8 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.34 g of 4-(3-trifluoromethylphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.25 g of N-[4-(3-trifluoromethylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 338).
The present compound 338
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=5.9 Hz), 6.27 (1H, dd, J=8.3, 2.7 Hz), 7.08 (2H, d, J=8.5 Hz), 7.24-7.28 (2H, m), 7.38 (2H, d, J=8.5 Hz), 7.47 (1H, d, J=8.0 Hz), 7.55-7.63 (3H, m), 8.14-8.19 (1H, m), 8.97 (1H, t, J=5.9 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.29 g of 4-(3-methoxyphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.17 g of N-[4-(3-methoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 339).
The present compound 339
1H-NMR (DMSO-D6) δ: 3.73 (3H, s), 4.42 (2H, d, J=5.9 Hz), 6.26 (1H, dd, J=8.3, 2.7 Hz), 6.51 (1H, dd, J=7.8, 2.0 Hz), 6.55 (1H, t, J=2.3 Hz), 6.70 (1H, dd, J=8.3, 2.4 Hz), 6.99 (2H, d, J=8.5 Hz), 7.24-7.29 (1H, m), 7.33 (2H, d, J=8.5 Hz), 7.57 (2H, s), 8.13-8.18 (1H, m), 8.95 (1H, t, J=5.9 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.29 g of 4-(4-methoxyphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.27 g of N-[4-(4-methoxyphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 340).
The present compound 340
1H-NMR (DMSO-D6) δ: 3.74 (3H, s), 4.39 (2H, d, J=5.8 Hz), 6.26 (1H, dd, J=8.5, 1.9 Hz), 6.89 (2H, d, J=7.7 Hz), 6.93-7.01 (4H, m), 7.28 (2H, d, J=8.5 Hz), 7.56 (2H, s), 8.12-8.17 (1H, m), 8.92 (1H, t, J=5.8 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.27 g of 4-(3-methylphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.22 g of N-[4-(3-methylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 341).
The present compound 341
1H-NMR (DMSO-D6) δ: 2.27 (3H, s), 4.41 (2H, d, J=5.6 Hz), 6.26 (1H, dd, J=8.5, 2.9 Hz), 6.73-6.81 (2H, m), 6.90-6.98 (3H, m), 7.21-7.27 (1H, m), 7.32 (2H, d, J=8.7 Hz), 7.56 (2H, s), 8.11-8.18 (1H, m), 8.95 (1H, t, J=5.1 Hz).
0.39 g of triethylamine was added to a mixture solution of 0.20 g of 2-amino-6-fluoronicotinic acid, 0.32 g of 4-(4-methylphenyloxy)benzylamine and 3 ml of DMF. Thereafter, 0.62 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, ice water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 0.31 g of N-[4-(4-methylphenyloxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 342).
The present compound 342
1H-NMR (DMSO-D6) δ: 2.28 (3H, s), 4.40 (2H, d, J=5.8 Hz), 6.26 (1H, dd, J=8.5, 2.7 Hz), 6.89 (2H, d, J=8.5 Hz), 6.93 (2H, d, J=8.5 Hz), 7.18 (2H, d, J=8.5 Hz), 7.31 (2H, d, J=8.5 Hz), 7.56 (2H, s), 8.12-8.18 (1H, m), 8.94 (1H, t, J=5.8 Hz).
1.50 ml of a 20% sodium ethoxide ethanol solution was added to a mixture of 0.31 g of N-(4-phenoxyphenyl)methyl-2-amino-6-chloronicotinic acid amide and 3 ml of N-methyl-2-pyrrolidone. The obtained mixture was stirred at 130° C. for 1 hour. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.19 g of N-(4-phenoxyphenyl)methyl-2-amino-6-ethoxynicotinic acid amide (hereinafter referred to as the present compound 343).
The present compound 343
1H-NMR (CDCl3) δ: 1.35 (3H, t, J=7.1 Hz), 4.29 (2H, q, J=7.1 Hz), 4.55 (2H, d, J=5.6 Hz), 5.98 (1H, d, J=8.5 Hz), 6.11 (1H, br s), 6.50 (2H, br s), 6.97-7.02 (4H, m), 7.08-7.12 (1H, m), 7.29-7.35 (4H, m), 7.49 (1H, d, J=8.5 Hz).
0.31 g of 2-chloro-6-methoxymethylnicotinic acid and 5 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 10 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-methoxymethylnicotinic acid.
The above crude 2-amino-6-methoxymethylnicotinic acid, 0.37 g of 2-fluoro-3-(4-pentynyloxy)benzylamine hydrochloride and 0.56 ml of triethylamine were added to 5 ml of DMF. Thereafter, 0.74 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.09 g of N-{3-[2-fluoro-3-(4-pentynyloxy)phenyl]}methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 344).
The present compound 344
1H-NMR (CDCl3) δ: 2.00-2.04 (3H, m), 2.43-2.45 (2H, m), 3.45 (3H, s), 4.14 (2H, t, J=6.0 Hz), 4.39 (2H, s), 4.64 (2H, d, J=5.8 Hz), 6.40 (3H, br s), 6.70 (1H, d, J=8.0 Hz), 6.94-7.01 (3H, m), 7.61 (1H, d, J=8.0 Hz).
0.29 g of 2-chloro-6-methoxymethylnicotinic acid and 50 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 16 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-methoxymethylnicotinic acid.
The above crude 2-amino-6-methoxymethylnicotinic acid, 0.27 g of 2-fluoro-3-methoxybenzylamine and 0.52 ml of triethylamine were added to 5 ml of DMF. Thereafter, 0.69 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 11 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, and it was then subjected to silica gel column chromatography, so as to obtain 0.16 g of N-[3-(2-fluoro-3-methoxy)phenyl]methyl-2-amino-6-methoxymethylnicotinic acid amide (hereinafter referred to as the present compound 345).
The present compound 345
1H-NMR (CDCl3) δ: 3.45 (3H, s), 3.90 (3H, s), 4.39 (2H, s), 4.65 (2H, d, J=5.6 Hz), 6.36-6.38 (3H, br m), 6.69 (1H, d, J=8.0 Hz), 6.93-6.97 (2H, m), 7.05 (1H, m), 7.60 (1H, d, J=8.0 Hz).
A mixture of 0.60 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 12 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-methoxymethylnicotinic acid.
The obtained crude 2-amino-6-fluoronicotinic acid, 0.72 g of 2-fluoro-3-methoxybenzylamine and 1.39 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.84 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours 30 minutes. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.26 g of N-[3-(2-fluoro-3-methoxy)phenyl]methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 346).
The present compound 346
1H-NMR (CDCl3) δ: 3.90 (3H, s), 4.64 (2H, d, J=5.6 Hz), 6.15 (1H, dd, J=8.3, 2.8 Hz), 6.28 (1H, br s), 6.57 (2H, br s), 6.91-7.09 (3H, m), 7.68 (1H, t, J=8.3 Hz).
A mixture of 0.62 g of 2,6-difluoronicotinic acid and 15 ml of 28% aqueous ammonia was stirred at a room temperature for 11 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, so as to obtain crude 2-amino-6-fluoronicotinic acid.
The obtained crude 2-amino-6-fluoronicotinic acid, 0.94 g of 2-fluoro-3-(4-pentynyloxy)benzylamine hydrochloride and 1.42 ml of triethylamine were added to 10 ml of DMF. Thereafter, 1.88 g of a BOP reagent was added to the mixture, and the obtained mixture was then stirred at a room temperature for 7 hours. Thereafter, water was added to the reaction mixture, and the mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, and it was then washed with a mixed solution of MTBE and hexane, so as to obtain 0.26 g of N-{3-[2-fluoro-3-(4-pentynyloxy)]phenyl}methyl-2-amino-6-fluoronicotinic acid amide (hereinafter referred to as the present compound 347).
The present compound 347
1H-NMR (CDCl3) δ: 1.99-2.04 (3H, m), 2.43-2.46 (2H, m), 4.15 (2H, t, J=6.0 Hz), 4.63 (2H, d, J=5.6 Hz), 6.15 (1H, d, J=8.3 Hz), 6.28 (1H, br s), 6.58 (2H, br s), 6.96-7.03 (3H, m), 7.69 (1H, t, J=8.3 Hz).
Next, with regard to production of the intermediate of the present compound, reference production examples will be given below.
12.5 g of triethylamine was added to a mixture of 10.1 g of 3-hydroxybenzylamine hydrobromide and 100 ml of DMF. Subsequently, 6.8 g of 2-aminonicotinic acid was added thereto, and 25.0 g of a BOP reagent was further added thereto. The obtained mixture was stirred at a room temperature for 30 minutes, and then at 80° C. for 5 hours. Thereafter, the reaction mixture was cooled to a room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was washed with water, hexane, and MTBE, so as to obtain 10.9 g of N-(3-hydroxyphenylmethyl)-2-aminonicotinic acid amide.
1H-NMR (DMSO-D6) δ: 4.36 (2H, d, J=5.8 Hz), 6.58-6.64 (2H, m), 6.69-6.74 (2H, m), 7.06-7.14 (3H, m), 7.95 (1H, dd, J=7.7, 1.4 Hz), 8.08 (1H, dd, J=4.8, 1.7 Hz), 8.94 (1H, t, J=5.9 Hz), 9.33 (1H, s).
A mixture of 11.97 g of butyltriphenylphosphonium bromide and 60 ml of DMF was stirred at −10° C. or lower. Thereafter, 1.04 g of 60% sodium hydride (in oil) was added to the mixture, and a mixture solution of 2.62 g of 3-cyanobenzaldehyde and 20 ml of DMF was further added thereto. The obtained mixture was stirred at a room temperature over a day and a night. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The obtained organic layer was successively washed with diluted hydrochloric acid, water, and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 3-(1-pentenyl)benzonitrile.
A mixture of the thus obtained 3-(1-pentenyl)benzonitrile, 0.1 g of 10% palladium on carbon, and 30 ml of ethanol was stirred under a hydrogen atmosphere. Three hours later, the reaction product was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure, so as to obtain 3-pentylbenzonitrile.
A mixture of 1.0 g of lithium aluminum hydride and 30 ml of THF was stirred under cooling on ice. A mixture solution of the above-obtained 3-pentylbenzonitrile and 10 ml of THF was added to the reaction mixture. The obtained mixture was stirred at a room temperature for 30 minutes, and then under heating to reflux for 2 hours. Thereafter, the reaction mixture solution was cooled to 0° C., and a sodium hydroxide aqueous solution was then added thereto. The obtained mixture was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure. MTBE was added to the residue, and the mixture was then dried over magnesium sulfate, followed by concentration under reduced pressure, so as to obtain 2.7 g of 3-pentylbenzylamine.
1H-NMR (CDCl3) δ: 0.89 (3H, t, J=7.0 Hz), 1.30-1.35 (4H, m), 1.45 (2H, br s), 1.58-1.66 (2H, m), 2.60 (2H, t, J=7.8 Hz), 3.85 (2H, s), 7.05-7.26 (4H, m).
A mixture of 6.0 g of 3-fluorobenzonitrile, 6.0 g of 3-methylphenol, 17 g of cesium carbonate and 50 ml of DMF was heated to reflux for 2 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 8.1 g of 3-(3-methylphenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 2.36 (3H, s), 6.81-6.86 (2H, m), 7.00-7.03 (1H, m), 7.18-7.49 (5H, m).
8.1 g of 3-(3-methylphenoxy)benzonitrile was added dropwise at 0° C. to a mixture solution of 1.8 g of lithium aluminum hydride and 50 ml of THF. The obtained solution was stirred at a room temperature for 3 hours. Thereafter, water, a 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. The reaction mixture was filtrated with Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE and potassium carbonate were added to the residue, and the mixture was then filtrated with Celite (registered trade mark), followed by concentration under reduced pressure, so as to obtain 7.5 g of 3-(3-methylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.44 (2H, br s), 2.32 (3H, s), 3.84 (2H, s), 6.79-6.96 (5H, m), 7.01-7.06 (1H, m), 7.19-7.30 (2H, m).
24.2 g of diisopropyl azodicarboxylate (40% toluene solution) was added dropwise at 0° C. to a mixture of 4.8 g of phenethyl alcohol, 4.8 g of 3-hydroxybenzaldehyde, 12.6 g of triphenylphosphine and 200 ml of THF. The obtained mixture was stirred at a room temperature for 8 hours. The reaction mixture solution was concentrated under reduced pressure, and the residue was subjected to silica gel chromatography, so as to obtain 3.9 g of 3-(2-phenylethoxy)benzaldehyde.
1H-NMR (CDCl3) δ: 3.12 (2H, t, J=7.0 Hz), 4.24 (2H, t, J=7.0 Hz), 7.14-7.46 (9H, m), 9.96 (1H, s).
2.1 g of methoxyamine hydrochloride was added to a mixture solution of 3.9 g 3-(2-phenylethoxy)benzaldehyde, 30 ml of tetrahydrofuran, 5 ml of water and 2.4 ml of pyridine. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was concentrated under reduced pressure. Thereafter, diluted hydrochloric acid was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 3.4 g of a mixture of 3-(2-phenylethoxy)benzaldehyde-O-methyl-oxime isomers.
Mixture of 3-(2-phenylethoxy)benzaldehyde-O-methyl-oxime isomers
1H-NMR (CDCl3) δ: 3.11 (2.0H, t, J=7.0 Hz), 3.96 (2.7H, s), 4.02 (0.3H, s), 4.20 (2.0H, t, J=7.1 Hz), 6.90-6.93 (1.0H, m), 7.08-7.11 (1.0H, m), 7.15-7.16 (1.0H, m), 7.24-7.34 (6.0H, m), 7.48 (0.1H, s), 8.01 (0.9H, s).
A mixture of 0.53 g of lithium aluminum hydride and 50 ml of THF was stirred under cooling on ice. Thereafter, a mixture solution of 3.0 of the mixture of 3-(2-phenylethoxy)benzaldehyde-O-methyl-oxime isomers and 20 ml of THF was added to the reaction mixture. The obtained mixture was stirred at a room temperature for 8 hours. Thereafter, the reaction mixture solution was cooled to 0° C. 0.5 ml of water, 0.5 ml of a 15% sodium hydroxide aqueous solution, and 1.5 ml of water were successively added to the reaction mixture. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and it was then concentrated under reduced pressure, so as to obtain 2.0 g of 3-(2-phenylethoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.10 (2H, t, J=7.1 Hz), 3.82 (2H, s), 4.18 (2H, t, J=7.1 Hz), 6.76-6.79 (1H, m), 6.86-6.89 (2H, m), 7.21-7.34 (6H, m).
5.0 g of 4-fluoro-3-phenoxybenzaldehyde, 2.4 g of hydroxylamine hydrochloride and 3.5 g of triethylamine were added to 10 ml of ethanol. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 3.5 g of 4-fluoro-3-phenoxybenzaldehyde oxime.
1H-NMR (CDCl3) δ: 6.98-7.02 (2H, m), 7.10-7.21 (2H, m), 7.25-7.36 (4H, m), 7.87 (1H, br s), 8.02 (1H, s).
1.2 g of lithium aluminum hydride was added to 50 ml of THF. A mixture solution of 3.5 g of 4-fluoro-3-phenoxybenzaldehyde oxime and 5 ml of THF was added dropwise to the above mixture at 0° C. The obtained mixture was stirred at a room temperature for 8 hours. Thereafter, water, 15% sodium hydroxide and water were successively added to the reaction mixture, and the obtained mixture was then stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was filtrated with Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure, so as to obtain 2.9 g of 4-fluoro-3-phenoxybenzylamine.
1H-NMR (CDCl3) δ: 1.47 (2H, br s), 3.79 (2H, s), 6.96-7.15 (6H, m), 7.29-7.34 (2H, m).
3.0 g of 2-chlorothiazolylmethylamine hydrobromide and 4.4 g of potassium 1,1-dimethylethoxide were added to 10 ml of n-butanol, and the obtained mixture was heated to reflux for 1 hour. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and the obtained mixture was then washed with MTBE. The water layer was converted to be alkaline with sodium hydroxide, and it was then extracted with MTBE twice. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure, so as to obtain 1.5 g of 2-butoxythiazol-5-ylmethylamine.
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.4 Hz), 1.38-1.56 (4H, m), 1.75-1.79 (2H, m), 3.91 (2H, s), 4.36 (2H, t, J=6.6 Hz), 6.90 (1H, s).
0.95 g of 4-(2-methoxyphenoxy)benzonitrile and 0.25 g of lithium aluminum hydride were added to 20 ml of THF. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, a 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was filtrated with Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE was added to the residue, and magnesium sulfate was then added to the mixture. The obtained mixture was dried, and it was then filtrated with Celite (registered trade mark). The filtrate was concentrated under reduced pressure, so as to obtain 1.0 g of 4-(2-methoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.64 (2H, br s), 3.84 (2H, s), 6.89-7.05 (5H, m), 7.10-7.14 (1H, m), 7.21-7.26 (2H, m).
2.0 g of potassium carbonate was added to a mixture of 2.0 g of 2-fluoro-4-hydroxybenzonitrile, 2.4 g of benzylbromide and 30 ml of acetonitrile. The obtained mixture was stirred at 50° C. for 3 hours. Thereafter, the reaction mixture was cooled to a room temperature, and it was then filtrated through Celite (registered trade mark), followed by concentration under reduced pressure. The obtained residue was collected by filtration, and it was then washed with hexane and was then dried, so as to obtain 2.8 g of 4-benzyloxy-2-fluorobenzonitrile.
1H-NMR (CDCl3) δ: 5.11 (2H, s), 6.81 (2H, m), 7.36-7.44 (5H, m), 7.52 (1H, dd, J=8.6, 7.6 Hz).
A mixture of 0.93 g of lithium aluminum hydride and 30 ml of THF was stirred under cooling on ice. Thereafter, a mixture solution of 2.8 g of 4-benzyloxy-2-fluorobenzonitrile and 10 ml of THF was added dropwise to the reaction mixture. The obtained mixture was stirred at a room temperature for 6 hours. Thereafter, the reaction mixture solution was cooled to 0° C. 0.9 ml of water, 0.9 ml of a 15% sodium hydroxide aqueous solution, and 2.7 ml of water were successively added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 1 hour. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and it was then concentrated under reduced pressure, so as to obtain 2.5 g of 4-benzyloxy-2-fluorobenzylamine.
1H-NMR (CDCl3) δ: 3.82 (2H, s), 5.04 (2H, s), 6.67-6.75 (2H, m), 7.18-7.24 (1H, m), 7.32-7.45 (5H, m).
A mixture of 5.0 g of 3,4-difluorobenzonitrile, 3.7 g of phenol, 50 ml of DMF and 14 g of cesium carbonate was stirred at a room temperature for 1 hour, and then at 80° C. for 3 hours. Thereafter, the reaction mixture solution was cooled to a room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was successively washed with a 15% sodium hydroxide aqueous solution, diluted hydrochloric acid, and a saturated saline solution. The resultant was dried over magnesium sulfate, and it was then concentrated under reduced pressure, so as to obtain 5.5 g of 3-fluoro-4-phenoxybenzonitrile.
1H-NMR (CDCl3) δ: 6.96 (1H, t, J=8.3 Hz), 7.04-7.08 (2H, m), 7.21-7.25 (1H, m), 7.35-7.44 (3H, m), 7.48 (1H, dd, J=10.0, 2.0 Hz).
A mixture of 1.7 g of lithium aluminum hydride and 40 ml of THF was stirred under cooling on ice. A mixture solution of 5.0 g of 3-fluoro-4-phenoxybenzonitrile and 20 ml of THF was added dropwise to the reaction mixture, and the obtained mixture was stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was cooled to 0° C. 1.7 ml of water, 1.7 ml of a 15% sodium hydroxide aqueous solution and 5.1 ml of water were successively added to the reaction mixture. The obtained mixture was stirred at a room temperature for 1 hour. The reaction mixture was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure, so as to obtain 4.3 g of 3-fluoro-4-phenoxybenzylamine.
1H-NMR (CDCl3) δ: 3.87 (2H, s), 6.96-7.10 (5H, m), 7.15-7.18 (1H, m), 7.29-7.34 (2H, m).
386 mg of 4-(4-chloro-3-ethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 332 mg of 4-(4-chloro-3-ethylphenoxy)benzylamine. 4-(4-chloro-3-ethylphenoxy)benzylamine
1H-NMR (CDCl3) δ: 1.20 (3H, t, J=7.5 Hz), 1.65 (2H, br s), 2.70 (2H, q, J=7.5 Hz), 3.86 (2H, s), 6.70-6.77 (1H, m), 6.89 (1H, d, J=2.8 Hz), 6.95 (2H, d, J=8.3 Hz), 7.23-7.31 (3H, m).
335 mg of 4-(2,4-dimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 292 mg of 4-(2,4-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.83 (2H, br s), 2.17 (3H, s), 2.31 (3H, s), 3.81 (2H, s), 6.77-6.85 (3H, m), 6.93-6.97 (1H, m), 7.05 (1H, s), 7.22 (2H, d, J=8.3 Hz).
356 mg of 4-(2,4,6-trimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 311 mg of 4-(2,4,6-trimethylphenoxy)benzylamine. 4-(2,4,6-trimethylphenoxy)benzylamine
1H-NMR (CDCl3) δ: 1.60 (2H, br s), 2.07 (6H, s), 2.30 (3H, s), 3.80 (2H, s), 6.71 (2H, d, J=8.7 Hz), 6.89 (2H, s), 7.18 (2H, d, J=8.7 Hz).
356 mg of 4-(2,3,6-trimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 316 mg of 4-(2,3,6-trimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.55 (2H, br s), 2.03 (3H, s), 2.07 (3H, s), 2.27 (3H, s), 3.80 (2H, s), 6.70 (2H, d, J=8.6 Hz), 6.95 (1H, d, J=7.8 Hz), 6.99 (1H, d, J=7.6 Hz), 7.18 (2H, d, J=8.6 Hz).
356 mg of 4-(4-propylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 302 mg of 4-(4-propylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 0.94 (3H, t, J=7.3 Hz), 1.53-1.73 (4H, m), 2.53-2.58 (2H, m), 3.84 (2H, s), 6.90 (2H, d, J=8.3 Hz), 6.95 (2H, d, J=8.3 Hz), 7.12 (2H, d, J=8.3 Hz), 7.26 (2H, d, J=8.3 Hz).
378 mg of 4-(4-butylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 330 mg of 4-(4-butylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.3 Hz), 1.31-1.41 (2H, m), 1.50-1.68 (4H, m), 2.58 (2H, t, J=7.7 Hz), 3.84 (2H, s), 6.91 (2H, d, J=8.6 Hz), 6.95 (2H, d, J=8.6 Hz), 7.12 (2H, d, J=8.3 Hz), 7.26 (2H, d, J=8.3 Hz).
394 mg of 4-(3,5-dichlorophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 296 mg of 4-(3,5-dichlorophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.58 (2H, br s), 3.89 (2H, s), 6.84 (2H, d, J=1.8 Hz), 7.00 (2H, d, J=8.4 Hz), 7.05 (1H, t, J=1.8 Hz), 7.34 (2H, d, J=8.4 Hz).
386 mg of 4-(2-chloro-4,5-dimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 293 mg of 4-(2-chloro-4,5-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 2.18 (3H, s), 2.23 (3H, s), 3.84 (2H, s), 6.80 (1H, s), 6.87-6.91 (2H, m), 7.21 (1H, s), 7.23-7.27 (2H, m).
419 mg of 4-(4-trifluoromethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 361 mg of 4-(4-trifluoromethoxyphenoxy)benzylamine. 4-(4-trifluoromethoxyphenoxy)benzylamine
1H-NMR (CDCl3) δ: 1.61 (2H, br s), 3.87 (2H, s), 6.95-7.00 (4H, m), 7.16 (2H, d, J=8.6 Hz), 7.31 (2H, d, J=8.3 Hz).
335 mg of 4-(2,5-dimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 1 ml of ethanol, 2 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 285 mg of 4-(2,5-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.64 (2H, br s), 2.18 (3H, s), 2.26 (3H, s), 3.83 (2H, s), 6.70 (1H, s), 6.83-6.89 (3H, m), 7.11 (1H, d, J=7.6 Hz), 7.24 (2H, d, J=8.6 Hz).
A mixture of 14.5 g of propyltriphenylphosphonium bromide and 100 ml of DMF was stirred at −10° C. or lower. Thereafter, 1.32 g of 60% sodium hydride (in oil) was added to the mixture, and a mixture solution of 1.97 g of 3-cyanobenzaldehyde and 10 ml of DMF was further added thereto. The obtained mixture was stirred at a room temperature over a day and a night. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The obtained organic layer was successively washed with diluted hydrochloric acid, water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 3-(1-butenyl)benzonitrile.
A mixture of the thus obtained 3-(1-butenyl)benzonitrile, 0.1 g of 10% palladium on carbon and 30 ml of ethanol was stirred under a hydrogen atmosphere. Three hours later, the reaction product was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure, so as to obtain 3-butylbenzonitrile.
A mixture of 0.63 g of lithium aluminum hydride and 20 ml of THF was stirred under cooling on ice. A mixture solution of the above-obtained 3-butylbenzonitrile and 10 ml of THF was added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under heating to reflux for 2 hours. Thereafter, the reaction mixture solution was cooled to 0° C., and a sodium hydroxide aqueous solution was then added thereto. The obtained mixture was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure. MTBE was added to the residue, and the mixture was then dried over magnesium sulfate, followed by concentration under reduced pressure, so as to obtain 1.6 g of 3-butylbenzylamine.
1H-NMR (CDCl3) δ: 0.93 (3H, t, J=7.4 Hz), 1.33-1.39 (2H, m), 1.46 (2H, br s), 1.57-1.64 (2H, m), 2.61 (2H, t, J=7.7 Hz), 3.84 (2H, s), 7.05-7.26 (4H, m).
A mixture of 12.4 g of pentyltriphenylphosphonium bromide and 30 ml of DMF was stirred at −10° C. or lower. Thereafter, 1.06 g of 60% sodium hydride (in oil) was added to the mixture, and a mixture solution of 2.62 g of 3-cyanobenzaldehyde and 5 ml of DMF was further added thereto. The obtained mixture was stirred at a room temperature over a day and a night. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The obtained organic layer was successively washed with diluted hydrochloric acid, water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel chromatography, so as to obtain 3-(1-hexenyl)benzonitrile.
A mixture of the thus obtained 3-(1-hexenyl)benzonitrile, 0.1 g of 10% palladium on carbon, and 50 ml of ethanol was stirred under a hydrogen atmosphere. Three hours later, the reaction product was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure, so as to obtain 3-hexylbenzonitrile.
A mixture of 0.91 g of lithium aluminum hydride and 30 ml of THF was stirred under cooling on ice. A mixture solution of the above-obtained 3-hexylbenzonitrile and 10 ml of THF was added to the reaction mixture, and the obtained mixture was stirred at a room temperature for 30 minutes, and then under heating to reflux for 2 hours. Thereafter, the reaction mixture solution was cooled to 0° C., and a sodium hydroxide aqueous solution was then added thereto. The obtained mixture was filtrated through Celite (registered trade mark), and the resultant was then concentrated under reduced pressure. MTBE was added to the residue, and the mixture was then dried over magnesium sulfate, followed by concentration under reduced pressure, so as to obtain 2.5 g of 3-hexylbenzylamine.
1H-NMR (CDCl3) δ: 0.88 (3H, t, J=6.7 Hz), 1.30-1.39 (8H, m), 1.57-1.65 (2H, m), 2.60 (2H, t, J=7.8 Hz), 3.84 (2H, s), 7.11-7.20 (4H, m).
0.37 g of 4-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.35 g of 4-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.47 (2H, br s), 1.76-1.81 (4H, m), 2.70-2.75 (4H, m), 3.84 (2H, s), 6.71 (1H, d, J=2.5 Hz), 6.75 (1H, dd, J=8.2, 2.5 Hz), 6.94-6.98 (2H, m), 7.01 (1H, d, J=8.2 Hz), 7.24-7.27 (2H, m).
0.34 g of 4-(3-methylphenylthio)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.33 g of 4-(3-methylphenylthio)benzylamine.
1H-NMR (CDCl3) δ: 1.46 (2H, br s), 2.30 (3H, s), 3.86 (2H, s), 7.02-7.06 (1H, m), 7.09-7.12 (1H, m), 7.15-7.20 (2H, m), 7.24-7.27 (2H, m), 7.31-7.34 (2H, m).
0.36 g of 4-(3-methoxyphenylthio)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.30 g of 4-(3-methoxyphenylthio)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.76 (3H, s), 3.87 (2H, s), 6.76 (1H, ddd, J=8.3, 2.5, 0.8 Hz), 6.82-6.88 (2H, m), 7.19 (1H, dd, J=8.3, 8.0 Hz), 7.24-7.30 (2H, m), 7.35-7.38 (2H, m).
383 mg of 4-(2-methyl-4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 369 mg of 4-(2-methyl-4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.41 (2H, br s), 2.21 (3H, s), 2.48 (3H, s), 3.83 (2H, s), 6.83 (1H, d, J=8.3 Hz), 6.84-6.87 (2H, m), 7.08 (1H, dd, J=8.3, 2.1 Hz), 7.18 (1H, d, J=2.1 Hz), 7.22-7.25 (2H, m).
404 mg of 4-(2,3-dimethyl-4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 342 mg of 4-(2,3-dimethyl-4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.39 (2H, br s), 2.17 (3H, s), 2.37 (3H, s), 2.43 (3H, s), 3.82 (2H, s), 6.79 (1H, d, J=8.6 Hz), 6.84 (2H, d, J=8.6 Hz), 7.07 (1H, d, J=8.6 Hz), 7.23 (2H, d, J=8.6 Hz).
387 mg of 4-(4-chloro-3,5-dimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 386 mg of 4-(4-chloro-3,5-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.40 (2H, br s), 2.33 (6H, s), 3.86 (2H, s), 6.73 (2H, s), 6.94-6.97 (2H, m), 7.28 (2H, d, J=8.6 Hz).
410 mg of 4-(3-ethyl-4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 391 mg of 4-(3-ethyl-4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.21 (3H, t, J=7.5 Hz), 1.51 (2H, br s), 2.44 (3H, s), 2.73 (2H, q, J=7.5 Hz), 3.85 (2H, s), 6.82 (1H, dd, J=8.6, 2.8 Hz), 6.88 (1H, d, J=2.8 Hz), 6.95-6.98 (2H, m), 7.19 (1H, d, J=8.6 Hz), 7.25-7.29 (2H, m).
362 mg of 3-(4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 339 mg of 3-(4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 2.48 (3H, s), 3.84 (2H, s), 6.86 (1H, dd, J=8.0, 1.9 Hz), 6.94-6.97 (3H, m), 7.03-7.06 (1H, m), 7.24-7.31 (3H, m).
413 mg of 4-(3-chloro-4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 349 mg of 4-(3-chloro-4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.45 (2H, br s), 2.46 (3H, s), 3.86 (2H, s), 6.91 (1H, dd, J=8.7, 2.8 Hz), 6.96-6.99 (2H, m), 7.03 (1H, d, J=2.8 Hz), 7.18 (1H, d, J=8.7 Hz), 7.28-7.32 (2H, m).
434 mg of 4-(3-chloro-4-ethylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 404 mg of 4-(3-chloro-4-ethylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.32 (3H, t, J=7.3 Hz), 1.53 (2H, br s), 2.92 (2H, q, J=7.3 Hz), 3.87 (2H, s), 6.87 (1H, dd, J=8.6, 2.7 Hz), 6.97-7.00 (2H, m), 7.03 (1H, d, J=2.7 Hz), 7.27-7.34 (3H, m).
407 mg of 4-(3-methoxy-4-methylthiophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 409 mg of 4-(3-methoxy-4-methylthiophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.64 (2H, br s), 2.41 (3H, s), 3.84 (3H, s), 3.85 (2H, s), 6.55 (1H, dd, J=8.3, 2.4 Hz), 6.59 (1H, d, J=2.4 Hz), 6.98 (2H, d, J=8.6 Hz), 7.15 (1H, d, J=8.3 Hz), 7.28 (2H, d, J=8.6 Hz).
335 mg of 4-(2,6-dimethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 0.5 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 334 mg of 4-(2,6-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.51 (2H, br s), 2.12 (6H, s), 3.80 (2H, s), 6.70-6.73 (2H, m), 7.03-7.11 (3H, m), 7.16-7.20 (2H, m).
726 mg of 4-fluorobenzonitrile, 890 mg of 3-trifluoromethoxyphenol, and 1.95 g of cesium carbonate were added to 6 ml of DMF. The obtained mixture was stirred at 100° C. for 4 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure. Sodium hydroxide was added to the residue, and the mixture was then extracted with MTBE. The organic layer was washed with water. The resultant was dried over sodium sulfate, and it was then concentrated by centrifugation under reduced pressure, so as to obtain 1.32 g of 4-(3-trifluoromethoxyphenoxy)benzonitrile.
427 mg of 4-(3-trifluoromethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure. A saturated saline solution was added to the obtained residue, and the mixture was then extracted with MTBE. Thereafter, the organic layer was dried over magnesium sulfate, and the resultant was concentrated by centrifugation under reduced pressure, so as to obtain 293 mg of 4-(3-trifluoromethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.68 (2H, br s), 3.87 (2H, s), 6.81-7.03 (5H, m), 7.27-7.37 (3H, m).
605 mg of 4-fluorobenzonitrile, 759 mg of 4-ethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 953 mg of 4-(4-ethoxyphenoxy)benzonitrile.
359 mg of 4-(4-ethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 340 mg of 4-(4-ethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.37 (2H, br s), 1.42 (3H, t, J=7.0 Hz), 3.83 (2H, s), 4.02 (2H, q, J=7.0 Hz), 6.85-6.97 (6H, m), 7.22-7.26 (2H, m).
605 mg of 4-fluorobenzonitrile, 836 mg of 4-propoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1010 mg of 4-(4-propoxyphenoxy)benzonitrile.
380 mg of 4-(4-propoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 355 mg of 4-(4-propoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.04 (3H, t, J=7.3 Hz), 1.36 (2H, br s), 1.76-1.85 (2H, m), 3.83 (2H, t, J=6.9 Hz), 3.90 (2H, t, J=6.6 Hz), 6.85-7.00 (6H, m), 7.22-7.26 (2H, m).
605 mg of 4-fluorobenzonitrile, 759 mg of 3-ethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 948 mg of 4-(3-ethoxyphenoxy)benzonitrile.
359 mg of 4-(3-ethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 367 mg of 4-(3-ethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.39 (3H, t, J=7.0 Hz), 1.42 (2H, br s), 3.85 (2H, s), 3.99 (2H, q, J=7.0 Hz), 6.54-6.58 (2H, m), 6.63 (1H, ddd, J=8.2, 2.4, 1.0 Hz), 6.98-7.01 (2H, m), 7.18-7.22 (1H, m), 7.26-7.30 (2H, m).
605 mg of 4-fluorobenzonitrile, 914 mg of 3-butoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 949 mg of 4-(3-butoxyphenoxy)benzonitrile.
458 mg of 4-(3-butoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 349 mg of 4-(3-butoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.39 (2H, br s), 1.41-1.52 (2H, m), 1.71-1.78 (2H, m), 3.82-3.88 (2H, br m), 3.92 (2H, t, J=6.4 Hz), 6.54-6.57 (2H, m), 6.61-6.65 (1H, m), 6.98-7.01 (2H, m), 7.17-7.22 (1H, m), 7.26-7.29 (2H, m).
0.61 g of 4-fluorobenzonitrile, 0.74 g of 5-hydroxyindane, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.88 g of 4-(indan-5-yloxy)benzonitrile.
0.42 g of 4-(indan-5-yloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.42 g of 4-(indan-5-yloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.42 (2H, br s), 2.06-2.13 (2H, m), 2.87 (4H, t, J=7.3 Hz), 3.84 (2H, s), 6.79 (1H, dd, J=8.2, 2.2 Hz), 6.86 (1H, d, J=2.2 Hz), 6.94-6.97 (2H, m), 7.16 (1H, d, J=8.2 Hz), 7.23-7.27 (2H, m).
0.61 g of 4-fluorobenzonitrile, 0.79 g of 2-hydroxynaphthalene and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was stirred at 100° C. for 7 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.48 g of 4-(2-naphthyloxy)benzonitrile.
0.37 g of 4-(2-naphthyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.39 g of 4-(2-naphthyloxy)benzylamine. 4-(2-naphthyloxy)benzylamine
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.88 (2H, s), 7.03-7.06 (2H, m), 7.24-7.33 (4H, m), 7.37-7.47 (2H, m), 7.69 (1H, d, J=8.1 Hz), 7.82 (1H, d, J=8.1 Hz), 7.83 (1H, d, J=8.6 Hz).
605 mg of 3-fluorobenzonitrile, 594 mg of 2-methylphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 866 mg of 3-(2-methylphenoxy)benzonitrile.
312 mg of 3-(2-methylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 309 mg of 3-(2-methylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.40 (2H, br s), 2.24 (3H, s), 3.83 (2H, s), 6.76 (1H, dd, J=8.1, 2.0 Hz), 6.87-6.93 (2H, m), 6.98-7.01 (1H, m), 7.05-7.10 (1H, m), 7.14-7.20 (1H, m), 7.24-7.28 (2H, m).
605 mg of 3-fluorobenzonitrile, 616 mg of 2-fluorophenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 895 mg of 3-(2-fluorophenoxy)benzonitrile.
320 mg of 3-(2-fluorophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 320 mg of 3-(2-fluorophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.85 (2H, s), 6.84 (1H, dd, J=8.2, 2.1 Hz), 6.94-6.96 (1H, m), 7.03-7.21 (5H, m), 7.26-7.30 (1H, m).
605 mg of 3-fluorobenzonitrile, 704 mg of 2-chlorophenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 992 mg of 3-(2-chlorophenoxy)benzonitrile.
344 mg of 3-(2-chlorophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 337 mg of 3-(2-chlorophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.45 (2H, br s), 3.86 (2H, s), 6.87 (1H, dd, J=8.1, 2.0 Hz), 6.92-6.97 (3H, m), 7.06-7.09 (1H, m), 7.26-7.32 (3H, m).
605 mg of 3-fluorobenzonitrile, 704 mg of 3-chlorophenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 968 mg of 3-(3-chlorophenoxy)benzonitrile.
344 mg of 3-(3-chlorophenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 336 mg of 3-(3-chlorophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.45 (2H, br s), 3.87 (2H, s), 6.87-6.92 (2H, m), 6.97-7.01 (2H, m), 7.05-7.12 (2H, m), 7.22-7.26 (1H, m), 7.30-7.34 (1H, m).
605 mg of 3-fluorobenzonitrile, 979 mg of 3-trifluoromethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1100 mg of 3-(3-trifluoromethoxyphenoxy)benzonitrile.
419 mg of 3-(3-trifluoromethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 401 mg of 3-(3-trifluoromethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.88 (2H, s), 6.84-6.87 (1H, m), 6.89-6.97 (3H, m), 7.00-7.03 (1H, m), 7.10-7.14 (1H, m), 7.30-7.36 (2H, m).
605 mg of 3-fluorobenzonitrile, 759 mg of 3-ethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 991 mg of 3-(3-ethoxyphenoxy)benzonitrile.
359 mg of 3-(3-ethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 354 mg of 3-(3-ethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.32-1.49 (2H, br m), 1.40 (3H, t, J=7.0 Hz), 3.85 (2H, s), 4.00 (2H, q, J=7.0 Hz), 6.55-6.59 (2H, m), 6.64 (1H, ddd, J=8.3, 2.0, 1.0 Hz), 6.90 (1H, dd, J=8.0, 2.0 Hz), 6.97-6.99 (1H, m), 7.04-7.07 (1H, m), 7.19-7.23 (1H, m), 7.27-7.31 (1H, m).
605 mg of 3-fluorobenzonitrile, 671 mg of 3-ethylphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 928 mg of 3-(3-ethylphenoxy)benzonitrile.
335 mg of 3-(3-ethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 336 mg of 3-(3-ethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.22 (3H, t, J=7.6 Hz), 1.40 (2H, br s), 2.63 (2H, q, J=7.6 Hz), 3.85 (2H, s), 6.81 (1H, dd, J=8.1, 1.8 Hz), 6.86-6.90 (2H, m), 6.93-6.98 (2H, m), 7.03-7.06 (1H, m), 7.22-7.31 (2H, m).
605 mg of 3-fluorobenzonitrile, 979 mg of 4-trifluoromethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1130 mg of 3-(4-trifluoromethoxyphenoxy)benzonitrile.
419 mg of 3-(4-trifluoromethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 349 mg of 3-(4-trifluoromethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.50 (2H, br s), 3.87 (2H, s), 6.89 (1H, dd, J=8.1, 1.8 Hz), 6.98-7.02 (3H, m), 7.08-7.11 (1H, m), 7.16-7.20 (2H, m), 7.30-7.34 (1H, m).
605 mg of 3-fluorobenzonitrile, 759 mg of 4-ethoxyphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 941 mg of 3-(4-ethoxyphenoxy)benzonitrile.
359 mg of 3-(4-ethoxyphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 329 mg of 3-(4-ethoxyphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.42 (3H, t, J=7.0 Hz), 1.52 (2H, br s), 3.82 (2H, s), 4.02 (2H, q, J=7.0 Hz), 6.81 (1H, dd, J=8.2, 1.9 Hz), 6.85-6.90 (3H, m), 6.95-7.00 (3H, m), 7.23-7.27 (1H, m).
605 mg of 3-fluorobenzonitrile, 671 mg of 4-ethylphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 994 mg of 3-(4-ethylphenoxy)benzonitrile. 3-(4-ethylphenoxy)benzonitrile
335 mg of 3-(4-ethylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 328 mg of 3-(4-ethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.24 (3H, t, J=7.7 Hz), 1.48 (2H, br s), 2.64 (2H, q, J=7.7 Hz), 3.84 (2H, s), 6.86 (1H, dd, J=8.1, 2.0 Hz), 6.92-6.96 (3H, m), 7.00-7.04 (1H, m), 7.15-7.18 (2H, m), 7.25-7.30 (1H, m).
605 mg of 3-fluorobenzonitrile, 748 mg of 4-propylphenol, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1010 mg of 3-(4-propylphenoxy)benzonitrile.
356 mg of 3-(4-propylphenoxy)benzonitrile was added to 1 ml of THF. Thereafter, 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 348 mg of 3-(4-propylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 0.95 (3H, t, J=7.3 Hz), 1.45 (2H, br s), 1.59-1.69 (2H, m), 2.57 (2H, t, J=7.7 Hz), 3.84 (2H, s), 6.86 (1H, dd, J=7.8, 2.0 Hz), 6.91-6.96 (3H, m), 7.00-7.04 (1H, m), 7.12-7.16 (2H, m), 7.25-7.30 (1H, m).
0.61 g of 3-fluorobenzonitrile, 0.74 g of 5-hydroxyindane, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.90 g of 3-(indan-5-yloxy)benzonitrile.
0.35 g of 3-(indan-5-yloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.33 g of 3-(indan-5-yloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.44 (2H, br s), 2.06-2.14 (2H, m), 2.88 (4H, t, J=7.5 Hz), 3.83 (2H, s), 6.80 (1H, dd, J=8.1, 2.3 Hz), 6.84-6.89 (2H, m), 6.93-6.95 (1H, m), 6.99-7.03 (1H, m), 7.16 (1H, d, J=8.3 Hz), 7.25-7.29 (1H, m).
0.61 g of 3-fluorobenzonitrile, 0.76 g of 2-hydroxy-5,6,7,8-tetrahydronaphthalene, and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1.07 g of 3-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzonitrile.
0.37 g of 3-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.38 g of 3-(5,6,7,8-tetrahydronaphthalen-2-yloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.42 (2H, br s), 1.76-1.82 (4H, m), 2.71-2.76 (4H, m), 3.83 (2H, s), 6.72-6.78 (2H, m), 6.86 (1H, dd, J=8.0, 1.9 Hz), 6.93-6.95 (1H, m), 7.00-7.04 (2H, m), 7.25-7.29 (1H, m).
0.61 g of 3-fluorobenzonitrile, 0.76 g of 5-hydroxybenzo[1,3]dioxole and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.89 g of 3-(benzo[1,3]dioxol-5-yloxy)benzonitrile.
0.36 g of 3-(benzo[1,3]dioxol-5-yloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.35 g of 3-(benzo[1,3]dioxol-5-yloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.53 (2H, br s), 3.83 (2H, s), 5.98 (2H, s), 6.50 (1H, dd, J=8.3, 2.4 Hz), 6.58 (1H, d, J=2.4 Hz), 6.76 (1H, d, J=8.3 Hz), 6.83 (1H, dd, J=8.1, 2.3 Hz), 6.91-6.92 (1H, m), 6.99-7.03 (1H, m), 7.24-7.29 (1H, m).
0.61 g of 3-fluorobenzonitrile, 0.79 g of 2-hydroxynaphthalene and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1.3 g of 3-(2-naphthyloxy)benzonitrile.
0.37 g of 3-(2-naphthyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.39 g of 3-(2-naphthyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.61 (2H, br s), 3.85 (2H, s), 6.95 (1H, dd, J=8.0, 1.9 Hz), 7.01-7.03 (1H, m), 7.07-7.10 (1H, m), 7.24-7.35 (3H, m), 7.38-7.48 (2H, m), 7.69-7.72 (1H, m), 7.81-7.85 (2H, m).
8.0 g of triethylamine was added to a mixture of 7.0 g of 2-fluoro-3-hydroxybenzylamine hydrobromide and 70 ml of DMF. Subsequently, 7.7 g of 2-aminonicotinic acid was added thereto, and 18.1 g of a BOP reagent was further added thereto. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, 30 ml of pyridine was added to the reaction mixture, and the obtained mixture was stirred at 110° C. for 3 hours. Thereafter, the reaction mixture was cooled to a room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was washed with hexane and MTBE, so as to obtain 5.4 g of N-(2-fluoro-3-hydroxyphenylmethyl)-2-aminonicotinic acid amide. N-(2-fluoro-3-hydroxyphenylmethyl)-2-aminonicotinic acid amide
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=5.6 Hz), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.71-6.75 (1H, m), 6.84 (1H, td, J=8.2, 1.7 Hz), 6.90-6.94 (1H, m), 7.06 (2H, br s), 7.95 (1H, dd, J=7.7, 1.9 Hz), 8.08 (1H, dd, J=4.7, 1.8 Hz), 8.91 (1H, t, J=5.8 Hz), 9.77 (1H, s).
A mixture of 22 g of 2-fluorophenol, 2.8 g of copper (I) bromide, 23 g of potassium (1,1-dimethylethoxide), and 125 g of bromobenzene was stirred under heating at 150° C., so that 1,1-dimethylethanol was removed from the reaction system. Thereafter, the mixture was heated to reflux for 2 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and ethyl acetate was then added to the residue, followed by filtration with Celite (registered trade mark). The filtrate was concentrated under reduced pressure, and the residue was then subjected to silica gel column chromatography. The obtained 2-fluorodiphenyl ether was distilled under an ordinary pressure, so as to obtain 22 g of 2-fluorodiphenyl ether.
1H-NMR (CDCl3) δ: 6.96-7.00 (2H, m), 7.03-7.21 (5H, m), 7.29-7.35 (2H, m).
To a mixture of 14 g of 2-fluorodiphenyl ether, 17 ml of N,N,N′,N″,N″-pentamethyldiethylenetriamine and 200 ml of THF, 48.5 ml of a hexane solution of 1.6 mol/liter n-butyllithium was added at −70° C., and the obtained mixture was then stirred at −70° C. for 2 hours. Thereafter, dry ice was mixed with the reaction mixture, and the temperature of the mixture was then gradually raised to a room temperature. THF was distilled under reduced pressure, and 5% hydrochloric acid was then added to the reaction mixture at 0° C., followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was collected by filtration, and it was then washed with hexane. The resultant was dried under reduced pressure, so as to obtain 15 g of 2-fluoro-3-phenoxybenzenecarboxylic acid.
1H-NMR (CDCl3) δ: 7.00 (2H, d, J=8.5 Hz), 7.11-7.20 (2H, m), 7.26-7.30 (1H, m), 7.35 (2H, dd, J=7.9, 7.7 Hz), 7.79 (1H, ddd, J=7.9, 6.2, 1.5 Hz).
10 g of 2-fluoro-3-phenoxybenzenecarboxylic acid, 3.1 ml of thionyl chloride, 1 drop of DMF and 30 ml of toluene were stirred at 80° C. for 1 hour, and then at 110° C. for 2 hours. Thereafter, the reaction mixture was cooled to a room temperature, and it was then concentrated under reduced pressure, so as to obtain 11 g of 2-fluoro-3-phenoxybenzenecarboxylic acid chloride.
1H-NMR (CDCl3) δ: 7.00 (2H, d, J=8.0 Hz), 7.16 (1H, t, J=7.1 Hz), 7.22 (1H, td, J=8.2, 1.0 Hz), 7.30-7.39 (3H, m), 7.84 (1H, ddd, J=7.8, 6.2, 1.5 Hz).
The 2-fluoro-3-phenoxybenzenecarboxylic acid chloride was added dropwise to a mixture of 20 ml of 28% aqueous ammonia and 50 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 1 hour. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then collected by filtration. The resultant was washed with water and hexane, and it was then dried under reduced pressure, so as to obtain 8.9 g of 2-fluoro-3-phenoxybenzamide.
1H-NMR (CDCl3) δ: 6.06 (1H, s), 6.64 (1H, s), 7.00 (2H, d, J=7.2 Hz), 7.12-7.27 (3H, m), 7.36 (2H, t, J=7.2 Hz), 7.85-7.89 (1H, m).
A mixture of 4.4 g of 2-fluoro-3-phenoxybenzamide and 20 ml of THF was added dropwise to a mixture of 58 ml of a THF solution of 1 mol/liter borane-THF complex and 20 ml of THF. The obtained mixture was stirred under heating to reflux for 7 hours. Thereafter, 20 ml of a THF solution of 1 mol/liter borane-THF complex was added to the reaction mixture, and the obtained mixture was stirred under heating to reflux again for 2 hours. The reaction mixture was cooled to 0° C., and diluted hydrochloric acid was added to the mixture. The obtained mixture was further stirred under heating to reflux for 30 minutes. The reaction mixture was cooled to a room temperature, and it was then concentrated under reduced pressure. A 15% sodium hydroxide aqueous solution was added to the obtained residue, and the mixture was then extracted with MTBE. Concentrated hydrochloric acid was added to the organic layer, followed by concentration, so as to obtain 4.0 g of 2-fluoro-3-phenoxybenzylamine hydrochloride.
1H-NMR (DMSO-d6) δ: 4.10 (2H, s), 7.00 (2H, d, J=8.5 Hz), 7.13-7.21 (2H, m), 7.27 (1H, t, J=8.0 Hz), 7.37-7.42 (2H, m), 7.46-7.50 (1H, m), 8.73 (3H, s).
To a mixture of 3.04 g of 4-fluorodiphenyl ether, 3.08 g of N,N,N′, N″,N″-pentamethyldiethylenetriamine and 30 ml of THF, 11 ml of a hexane solution of 1.6 mol/liter n-butyllithium was added at −78° C. The obtained mixture was stirred at −78° C. for 2 hours. Thereafter, dry ice was mixed with the mixture, and the temperature of the mixture was then gradually raised to a room temperature. 5% hydrochloric acid was added to the reaction mixture at 0° C., and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was collected by filtration, and it was then washed with hexane, so as to obtain 3.82 g of 2-fluoro-5-phenoxybenzenecarboxylic acid.
1H-NMR (CDCl3) δ: 6.98-7.01 (2H, m), 7.12-7.17 (2H, m), 7.21-7.25 (1H, m), 7.34-7.39 (2H, m), 7.62 (1H, dd, J=5.9, 3.2 Hz).
2.94 g of thionyl chloride was added to a mixture of 3.82 g of 2-fluoro-5-phenoxybenzenecarboxylic acid and 30 ml of toluene at a room temperature. They were blended at 50° C. for 30 minutes, then at 80° C. for 2 hours, and then at 110° C. for 1 hour. Thereafter, the temperature of the reaction mixture was cooled to a room temperature, and the mixture was then concentrated under reduced pressure, so as to obtain crude 2-fluoro-5-phenoxybenzenecarboxylic acid chloride.
The thus obtained crude 2-fluoro-5-phenoxybenzenecarboxylic acid chloride was added dropwise to a mixture of 20 ml of 28% aqueous ammonia and 50 ml of THF at 0° C., and the obtained mixture was stirred at a room temperature for 1 hour. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then collected by filtration. The residue was washed with water and hexane, and it was then dried under reduced pressure, so as to obtain 3.0 g of 2-fluoro-5-phenoxybenzamide.
1H-NMR (CDCl3) δ: 5.95 (1H, br s), 6.69 (1H, br s), 6.97-7.01 (2H, m), 7.09-7.18 (3H, m), 7.32-7.37 (2H, m), 7.73 (1H, dd, J=6.3, 2.9 Hz).
20 ml of a borane-THF-complex-containing THF solution (0.99 M) was added dropwise to a mixture of 1.5 g of 2-fluoro-5-phenoxybenzamide and 10 ml of THF at 0° C. The obtained mixture was stirred for 30 minutes and it was then stirred under heating to reflux for 3 hours. Thereafter, the reaction mixture was cooled to 5° C., and diluted hydrochloric acid was then added thereto. The obtained mixture was further heated to reflux for 3 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then successively washed with water and hexane, so as to obtain 1.0 g of 2-fluoro-5-phenoxybezylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 4.04 (2H, q, J=5.7 Hz), 7.00-7.42 (8H, m), 8.56 (3H, br s).
A mixture of 4.84 g of 4-fluorobenzonitrile, 9.77 g of 3,5-dimethylphenol, 26.1 g of cesium carbonate and 100 ml of DMF was stirred at 130° C. for 6.5 hours.
Thereafter, the reaction mixture was cooled to a room temperature, and it was then filtrated. Thereafter, water was added to the obtained filtrate, followed by extraction with ethyl acetate. The extract was dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 8.40 g of 4-(3,5-dimethylphenoxy)-benzonitrile.
1H-NMR (CDCl3) δ: 2.32 (6H, d, J=0.5 Hz), 6.66-6.68 (2H, m), 6.85-6.87 (1H, m), 6.96-7.00 (2H, m), 7.56-7.61 (2H, m).
A mixture solution of 8.3 g of 4-(3,5-dimethylphenoxy)-benzonitrile and 20 ml of THF was added dropwise to a mixture solution of 2.11 g of lithium aluminum hydride and 50 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 10 hours. A small amount of ethyl acetate and water was successively added to the reaction mixture. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure, so as to obtain 7.1 g of 4-(3,5-dimethylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 2.28 (6H, d, J=0.5 Hz), 2.28 (3H, s), 2.28 (3H, s), 3.85 (2H, s), 6.61-6.63 (2H, m), 6.72-6.74 (1H, m), 6.95-6.98 (2H, m), 7.25-7.28 (2H, m).
A mixture of 7.57 g of 2-methylphenol and 15 ml of DMF was slowly added to a mixture of 2.94 g of 60% sodium hydride (in oil) and 35 ml of DMF. Subsequently, 5.39 g of 5-nitrothiophen-2-carbonitrile was slowly added thereto, and the obtained mixture was then stirred at a room temperature for 2 days. Thereafter, the reaction mixture was added to ice water, and it was then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 2.50 g of 5-(2-methylphenyloxy)-thiophen-2-carbonitrile.
1H-NMR (CDCl3) δ: 2.27 (3H, s), 6.32 (1H, d, J=4.1 Hz), 7.09 (1H, dd, J=7.8, 1.5 Hz), 7.16-7.30 (3H, m), 7.34 (1H, d, J=4.1 Hz).
18 ml of a borane-THF-complex-containing THF solution (0.99 M) was added dropwise to a mixture of 2.5 g of 5-(2-methylphenyloxy)-thiophen-2-carbonitrile and 20 ml of THF at 0° C. The obtained mixture was stirred for 30 minutes, and it was then stirred under heating to reflux for 3 hours. Thereafter, the reaction mixture was cooled to 5° C., and diluted hydrochloric acid was then added thereto. The obtained mixture was further heated to reflux for 3 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then successively washed with water and hexane, so as to obtain 2.53 g of [5-(2-methylphenyloxy)thiophen-2-yl]methylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 2.26 (3H, s), 4.08-4.14 (2H, m), 6.47 (1H, d, J=3.6 Hz), 6.98 (1H, d, J=3.6 Hz), 7.03-7.06 (1H, m), 7.12-7.16 (1H, m), 7.22-7.26 (1H, m), 7.32-7.34 (1H, m), 8.34 (3H, br s).
A mixture of 27 g of 4-chlorobenzotrifluoride, 12 g of 3-hydroxybenzaldehyde, 12.3 g of potassium 1,1-dimethylethoxide, 4.3 g of copper (I) bromide and 150 ml of DMF was heated to reflux for 2 hours. Thereafter, water and ethyl acetate were added to the reaction mixture. Thereafter, insoluble matter was removed by Celite (registered trade mark), and the organic layer was then separated. The organic layer was successively washed with hydrochloric acid, water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 6.5 g of 3-(4-trifluoromethylphenoxy)benzaldehyde.
1H-NMR (CDCl3) δ: 7.09 (2H, d, J=8.5 Hz), 7.33 (1H, ddd, J=8.1, 2.5, 1.0 Hz), 7.53-7.71 (5H, m), 9.99 (1H, s).
6.5 g of 3-(4-trifluoromethylphenoxy)benzaldehyde, 2.5 g of hydroxylamine hydrochloride, 50 ml of ethanol and 2.4 g of water were blended. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was left overnight. Subsequently, 2.5 ml of 10 N hydrochloric acid and 3.0 g of 10% palladium on carbon were added to the reaction mixture, and the obtained mixture was then stirred under an ordinary pressure in a hydrogen atmosphere for 10 hours. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The residue was washed with water and MTBE, so as to obtain 4.9 g of 3-(4-trifluoromethylphenoxy)benzylamine hydrochloride. 3-(4-trifluoromethylphenoxy)benzylamine hydrochloride
1H-NMR (CDCl3) δ: 1.52 (2H, br s), 3.88 (2H, s), 6.93 (1H, dd, J=8.0, 2.0 Hz), 7.02-7.06 (3H, m), 7.14 (1H, dd, J=7.6, 0.5 Hz), 7.34 (1H, dd, J=8.0, 7.6 Hz), 7.57 (2H, d, J=8.5 Hz).
20 ml of a borane-THF-complex-containing THF solution (0.93 M) was added dropwise to a solution produced by adding 3.5 g of 4-(4-bromophenoxy)benzonitrile and 50 ml of THF at 0° C. The obtained mixture was stirred under heating to reflux for 6 hours. Thereafter, diluted hydrochloric acid was then added the reaction mixture. The obtained mixture was further heated to reflux for 1 hour. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then successively washed with water and chloroform, so as to obtain 3.5 g of 4-(4-bromophenoxy)benzylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 4.00 (2H, s), 6.94-6.98 (2H, m), 7.07-7.10 (2H, m), 7.52-7.60 (4H, m), 8.45 (3H, br s).
A mixture of 12.4 g of 4-fluorobenzaldehyde, 12.0 g of phenol, 18.0 g of potassium carbonate and 60 ml of DMF was heated to reflux for 1 hour. After, water was added to the reaction mixture, it was then extracted with ethyl acetate. The organic layer was successively washed with diluted hydrochloric acid, water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 21.0 g of 4-phenoxybenzaldehyde.
21.0 g of 4-phenoxybenzaldehyde, 10.5 g of hydroxylamine hydrochloride, 200 ml of ethanol and 10 ml of water were blended. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was left overnight. Subsequently, 10 ml of 10 N hydrochloric acid and 3.2 g of 10% palladium on carbon were added to the reaction mixture, and the obtained mixture was then stirred under an ordinary pressure in a hydrogen atmosphere for 6 hours. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The residue was washed with water and chloroform, so as to obtain 19.3 g of 4-phenoxybenzylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 3.99 (2H, s), 6.99-7.04 (4H, m), 7.14-7.19 (1H, m), 7.39-7.44 (2H, m), 7.52-7.56 (2H, m), 8.56 (3H, br s).
35.0 g of 3-phenoxybenzaldehyde, 18.5 g of hydroxylamine hydrochloride, 200 ml of ethanol, and 18.2 g of water were blended. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, the reaction mixture was left overnight. Subsequently, 18 ml of 10 N hydrochloric acid and 2.5 g of 10% palladium on carbon were added to the reaction mixture, and the obtained mixture was then stirred under an ordinary pressure in a hydrogen atmosphere for 6 hours. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The residue was washed with water, so as to obtain 33.5 g of 3-phenoxybenzylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 4.00 (2H, s), 6.97-7.05 (3H, m), 7.14-7.19 (1H, m), 7.22-7.25 (1H, m), 7.28-7.31 (1H, m), 7.38-7.44 (3H, m), 8.59 (3H, br s).
A mixture of 10 g of 4-fluorobenzonitrile, 11 g of 3-methylphenol, 35 g of cesium carbonate and 100 ml of DMF was heated to reflux for 2 hours. Thereafter, ethyl acetate was added to the reaction mixture. Thereafter, insoluble matter was removed by Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 17.5 g of 4-(3-methylphenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 2.36 (3H, s), 6.84-6.89 (2H, m), 6.97-7.06 (3H, m), 7.26-7.31 (1H, m), 7.57-7.61 (2H, m).
A solution produced by dissolving 17.5 g of 4-(3-methylphenoxy)benzonitrile in 10 ml of THF was added dropwise to a mixture solution of 3.8 g of lithium aluminum hydride and 100 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then left overnight. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE and potassium carbonate were added to the residue. The resultant was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure so as to obtain 16 g of crude 4-(3-methylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 2.32 (3H, s), 3.85 (2H, s), 6.77-6.83 (2H, m), 6.88-6.92 (1H, m), 6.95-6.99 (2H, m), 7.17-7.22 (1H, m), 7.25-7.29 (2H, m).
A mixture of 5.0 g of 3-fluorobenzonitrile, 5.3 g of 4-methylphenol, 17.5 g of cesium carbonate and 30 ml of DMF was heated to reflux for 4 hours. Thereafter, ethyl acetate was added to the reaction mixture. Thereafter, insoluble matter was removed by Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 8.0 g of 3-(4-methylphenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 2.37 (3H, s), 6.91-6.95 (2H, m), 7.16-7.22 (4H, m), 7.31-7.41 (2H, m).
A solution produced by dissolving 8.0 g of 3-(4-methylphenoxy)benzonitrile in 5 ml of THF was added dropwise to a mixture solution of 1.8 g of lithium aluminum hydride and 50 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture, and the obtained mixture was then left overnight. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE and potassium carbonate were added to the residue. The resultant was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure so as to obtain 7.0 g of crude 3-(4-methylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.40 (2H, br s), 2.33 (3H, s), 3.82 (2H, s), 6.82-6.87 (1H, m), 6.89-6.95 (3H, m), 6.99-7.03 (1H, m), 7.11-7.15 (2H, m), 7.24-7.28 (1H, m).
A mixture of 6.0 g of 4-fluorobenzonitrile, 6.0 g of 3-fluorophenol, 16 g of cesium carbonate and 50 ml of DMF was heated to reflux for 4 hours. Thereafter, ethyl acetate was added to the reaction mixture. Thereafter, insoluble matter was removed by Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 10.0 g of 4-(3-fluorophenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 6.77-6.81 (1H, m), 6.83-6.87 (1H, m), 6.91-6.96 (1H, m), 7.03-7.07 (2H, m), 7.33-7.40 (1H, m), 7.62-7.65 (2H, m).
10.0 g of 4-(3-fluorophenoxy)benzonitrile was added dropwise to a mixture solution of 2.0 g of lithium aluminum hydride and 100 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture. The obtained mixture was stirred at a room temperature for 2 hours, and it was then left overnight. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE and potassium carbonate were added to the residue. The resultant was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure so as to obtain 7.5 g of 4-(3-fluorophenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.45 (2H, br s), 3.87 (2H, s), 6.66-6.83 (3H, m), 6.99-7.05 (2H, m), 7.22-7.35 (3H, m).
A mixture of 7.0 g of 4-chlorobenzonitrile, 6.0 g of 4-methylphenol, 10 g of cesium carbonate and 100 ml of DMF was heated to reflux for 2 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 9.1 g of 4-(4-methylphenoxy)benzonitrile.
1H-NMR (CDCl3) δ: 2.37 (3H, s), 6.94-6.99 (4H, m), 7.21 (2H, d, J=8.0 Hz), 7.56-7.59 (2H, m).
9.0 g of 4-(4-methylphenoxy)benzonitrile was added dropwise to a mixture solution of 2.0 g of lithium aluminum hydride and 100 ml of THF at 0° C. The obtained mixture was stirred at a room temperature for 3 hours. Thereafter, water, 15% sodium hydroxide aqueous solution and water were successively added to the reaction mixture. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. MTBE and potassium carbonate were added to the residue. The resultant was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure so as to obtain 8.5 g of 4-(4-methylphenoxy)benzylamine.
1H-NMR (CDCl3) δ: 1.48 (2H, br s), 2.33 (3H, s), 3.83 (2H, s), 6.88-6.97 (4H, m), 7.10-7.14 (2H, m), 7.23-7.27 (2H, m).
6.4 g of 2-chloro-6-methylnicotinic acid and 50 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred at 180° C. under pressure for 7 hours. Thereafter, the reaction mixture was left to cool to a room temperature, and it was then concentrated under reduced pressure. Hydrochloric acid was added to the obtained residue, and the precipitated solid was collected by filtration, so as to obtain 3.4 g of 2-amino-6-methylnicotinic acid.
1H-NMR (DMSO-D6) δ: 2.30 (3H, s), 6.47 (1H, d, J=7.8 Hz), 7.15 (2H, br s), 7.91 (1H, d, J=7.8 Hz).
48 g of pivaloyl chloride was added dropwise at 0° C. to a solution produced by adding 20 g of 2,6-diaminopyridine and 46 g of triethylamine to 200 ml of chloroform. The obtained mixture was stirred at a room temperature for 4 hours. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with chloroform. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 31 g of N-[6-(2,2-dimethylpropionylamino)pyridin-2-yl]-2,2-dimethylpropionic acid amide.
1H-NMR (CDCl3) δ: 1.32 (18H, s), 7.69 (1H, t, J=8.0 Hz), 7.74 (2H, br s), 7.92 (2H, d, J=8.0 Hz).
200 ml of a hexane solution of 1.58 M n-butyllithium was added dropwise at −70° C. to a solution produced by adding 25 g of N-(6-(2,2-dimethylpropionylamino)pyridin-2-yl)-2,2-dimethylpropionic acid amide to 250 ml of THF. The obtained mixture was stirred at 0° C. for 8 hours, and 25 g of dry ice was then added to the reaction mixture at −60° C. The obtained mixture was stirred at a room temperature for 2 hours, and 30 ml of 10 N hydrochloric acid was then added thereto, followed by extraction with ethyl acetate. The organic layer was successively washed with water and a saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 33 g of 2,6-di(2,2-dimethylpropionylamino)nicotinic acid.
1H-NMR (CDCl3) δ: 1.35 (9H, s), 1.37 (9H, s), 7.66 (1H, d, J=6.5 Hz), 8.59 (1H, d, J=6.5 Hz).
33 g of 2,6-di(2,2-dimethylpropionylamino)nicotinic acid and 25 g of sodium hydroxide were added to 175 g of water. The obtained mixture was heated to reflux for 2 hours. Thereafter, 50 ml of 10 N hydrochloric acid was added to the reaction mixture, and the precipitated solid was collected by filtration. The obtained solid was washed with water, and it was then dried under reduced pressure at 60° C. The obtained solid was successively washed with MTBE and ethyl acetate, and it was then dried under reduced pressure at 80° C., so as to obtain 13 g of 2,6-diaminonicotinic acid hydrochloride.
1H-NMR (DMSO-D6) δ: 5.84 (1H, d, J=8.7 Hz), 7.14 (2H, br s), 7.39 (2H, br s), 7.78 (1H, d, J=8.7 Hz).
21.6 g of 2-amino-6-methylpyridine and 24 g of triethylamine were added to 200 ml of chloroform, and 26 g of pivaloyl chloride was added dropwise at 0° C. to the mixture. The obtained mixture was stirred at a room temperature for 1 day. Thereafter, a sodium bicarbonate aqueous solution was added to the reaction mixture, and it was then extracted with chloroform twice. The organic layer was dried over magnesium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 36.8 g of N-(6-methylpyridin-2-yl)-2,2-dimethylpropionic acid amide. N-(6-methylpyridin-2-yl)-2,2-dimethylpropionic acid amide
1H-NMR (CDCl3) δ: 1.33 (9H, s), 2.45 (3H, s), 6.88 (1H, d, J=7.7 Hz), 7.58 (1H, dd, J=8.1, 7.7 Hz), 7.94 (1H, br s), 8.05 (1H, d, J=8.1 Hz).
73 ml of a pentane solution of 1.5 mol/l 1,1-dimethylethyllithium was added dropwise at −78° C. to a solution produced by adding 10.0 g of N-(6-methylpyridin-2-yl)-2,2-dimethylpropionic acid amide to 200 ml of diethyl ether. The obtained mixture was stirred at −78° C. for 3 hours, and then at 0° C. for 30 minutes. Thereafter, 10 g of dry ice was then added to the reaction mixture at −78° C. The reaction mixture was stirred until it reached a room temperature, and a citric acid aqueous solution was added to the reaction mixture until the mixture becomes acidic. The obtained mixture was extracted with ethyl acetate 10 times, and it was then washed with a saturated saline solution. The organic layer was dried over magnesium sulfate, followed by concentration under reduced pressure, so as to obtain 6.4 g of 2-(2,2-dimethylpropionylamino)-6-methylnicotinic acid.
1H-NMR (DMSO-D6) δ: 1.22 (9H, s), 2.46 (3H, s), 7.08 (1H, d, J=7.8 Hz), 8.08 (1H, d, J=7.8 Hz), 10.83 (1H, br s).
6.4 g of 2-(2,2-dimethylpropionylamino)-6-methylnicotinic acid was added to 50 ml of a 12.5% sodium hydroxide aqueous solution. The obtained mixture was heated to reflux for 2 hours. Thereafter, diluted hydrochloric acid was added to the reaction mixture, so that the pH thereof was adjusted to pH 3, and the precipitated solid was then collected by filtration. The obtained solid was added to methanol. The obtained mixture was concentrated under reduced pressure, and it was then dried, so as to obtain 2.2 g of 2-amino-6-methylnicotinic acid.
5.0 g of WSC and 3.5 g of 1-hydroxybenzotriazole were added to a mixture of 3.0 g of 2-aminonicotinic acid, 6.5 g of 4-benzyloxybenzylamine hydrochloride and 50 ml of pyridine. The obtained mixture was stirred at a room temperature for 3 hours, and it was then heated to reflux for 4 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and water was then added thereto. The obtained crystal was washed with hexane and was then dried, so as to obtain N-(4-benzyloxyphenyl)methyl-2-aminonicotinic acid amide.
A mixture of the thus obtained N-(4-benzyloxyphenyl)methyl-2-aminonicotinic acid amide, 10% palladium on carbon 2 ml of concentrated hydrochloric acid, and 20 ml of ethanol was stirred under a hydrogen atmosphere. After completion of the reaction, the reaction product was filtrated through Celite (registered trade mark), and the resultant was concentrated under reduced pressure and was then washed with MTBE, so as to obtain 1.2 g of N-(4-hydroxyphenyl)methyl-2-aminonicotinic acid amide.
1H-NMR (DMSO-D6) δ: 3.74 (2H, d, J=5.9 Hz), 6.00 (1H, dd, J=7.7, 4.8 Hz), 6.13 (2H, d, J=8.5 Hz), 6.52-6.54 (4H, m), 7.34 (1H, t, J=3.9 Hz), 7.49 (1H, dd, J=4.8, 1.8 Hz), 8.32 (1H, t, J=5.7 Hz), 8.77 (1H, br s).
4.62 g of 5-nitrothiophen-2-carbonitrile was slowly added to a mixture of 7.29 g of 3-trifluoromethylphenol and 40 ml of DMF under cooling on ice. Subsequently, 19.5 g of cesium carbonate was added thereto, and the obtained mixture was then stirred at a room temperature for 2 days. Thereafter, the reaction mixture was added to ice water, and it was then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and it was then concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 3.0 g of 5-(3-trifluoromethylphenyloxy)-thiophen-2-carbonitrile.
1H-NMR (CDCl3) δ: 6.51 (1H, d, J=4.1 Hz), 7.31-7.35 (1H, m), 7.39-7.41 (1H, m), 7.42 (1H, d, J=4.1 Hz), 7.49-7.56 (2H, m).
17 ml of a borane-THF-complex in THF solution (0.99 M) was added dropwise to a mixture of 3.0 g of 5-(3-trifluoromethylphenyloxy)-thiophen-2-carbonitrile and 20 ml of THF at 0° C. The obtained mixture was stirred for 30 minutes, and it was then stirred under heating to reflux for 3 hours. Thereafter, the reaction mixture was cooled to 5° C., and hydrochloric acid was then added thereto. The obtained mixture was further heated to reflux for 2 hours. Thereafter, the reaction mixture was concentrated under reduced pressure, and the obtained residue was then successively washed with hexane, so as to obtain 2.53 g of [5-(3-trifluoromethylphenyloxy)thiophen-2-yl]methylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 4.16 (2H, s), 6.75 (1H, d, J=3.9 Hz), 7.10 (1H, d, J=3.9 Hz), 7.43-7.45 (2H, m), 7.55-7.57 (1H, m), 7.66-7.69 (1H, m), 8.52 (3H, br s).
5.0 g of 2,6-dichloronicotinic acid and 40 ml of 28% aqueous ammonia were added to an autoclave, and they were then stirred under pressure for 5 hours. Thereafter, concentrated hydrochloric acid was added to the reaction mixture, so that the pH was adjusted to be pH 1. The resultant was extracted with ethyl acetate, and it was washed with a saturated saline solution and was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, so as to obtain 4.2 g of 2-amino-6-chloronicotinic acid.
1H-NMR (DMSO-D6) δ: 6.63 (1H, d, J=8.2 Hz), 7.55 (2H, br s), 8.03 (1H, d, J=8.2 Hz).
A mixture of 101 g of 2-chloro-6-methylnicotinic acid, 85.4 g of potassium carbonate, 40.3 ml of methyl iodide and 1 l of acetonitrile was heated to reflux for 4 hours 30 hours. Thereafter, the reaction mixture solution was cooled to a room temperature, and it was then filtrated through Celite. The solution was concentrated under reduced pressure, so as to obtain crude 2-chloro-6-methylnicotinic acid methyl ester.
1H-NMR (CDCl3) δ: 2.62 (3H, s), 3.97 (3H, s), 7.18 (1H, d, J=8.0 Hz), 8.10 (1H, d, J=8.0 Hz).
A mixture of the crude 2-chloro-6-methylnicotinic acid methyl ester, 21.1 g of 4,4′-thiobis(6-tertiary butyl-3-cresol), 174 g of 70% 3-chloroperbenzoic acid, and 800 ml of chloroform was heated to reflux for 6 hours. Further, the reaction mixture was left to cool to around room temperature, and 14.5 g of 70% 3-chloroperbenzoic acid was then added to the reaction mixture. The obtained mixture was heated to reflux for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and a saturated sodium bicarbonate aqueous solution was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. Crude 2-chloro-6-methylniconitic acid methyl ester-N-oxide was obtained.
1H-NMR (CDCl3) δ: 2.62 (3H, s), 3.99 (3H, s), 7.28 (1H, d, J=8.2 Hz), 7.62 (1H, d, J=8.2 Hz).
A mixture of the crude 2-chloro-6-methylniconitic acid methyl ester-N-oxide and 500 ml of acetic anhydride was stirred at 60° C. for 3 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure, so as to obtain crude 2-chloro-6-acetoxymethylnicotinic acid methyl ester.
1H-NMR (CDCl3) δ: 1.64 (3H, s), 3.40 (3H, s), 4.67 (2H, s), 6.81 (1H, d, J=8.1 Hz), 7.64 (1H, d, J=8.1 Hz).
A mixture of the 2-chloro-6-acetoxymethylnicotinic acid methyl ester, 48.4 g of potassium carbonate and 500 ml of methanol was stirred at a room temperature for 45 minutes. Thereafter, the reaction mixture solution was filtrated through Celite, and the solution was then concentrated under reduced pressure, followed by extraction with ethyl acetate. The extract was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate. Thereafter, the resultant was concentrated under reduced pressure, so as to obtain 28.8 g of 2-chloro-6-hydroxymethylnicotinic acid methyl ester.
1H-NMR (CDCl3) δ: 2.96 (1H, t, J=5.6 Hz), 3.95 (3H, s), 4.80 (2H, s), 7.35-7.38 (1H, d, J=7.8 Hz), 8.19 (1H, d, J=7.8 Hz).
A mixture of 2-chloro-6-hydroxymethylnicotinic acid methyl ester, 36.4 g of silver (I) oxide, 9.8 ml of methyl iodide and 400 ml of toluene was stirred at a room temperature for 5 hours 30 minutes. Thereafter, the reaction mixture solution was filtrated through Celite, and the solution was then concentrated under reduced pressure. Thereafter, the resultant was subjected to silica gel column chromatography, so as to obtain 25.7 g of 2-chloro-6-methoxymethylnicotinic acid methyl ester.
1H-NMR (CDCl3) δ: 3.49 (3H, s), 3.95 (3H, s), 4.58 (2H, s), 7.47 (1H, d, J=7.8 Hz), 8.20 (1H, d, J=7.8 Hz).
A mixture of 25.7 g of 2-chloro-6-methoxymethylnicotinic acid methyl ester, 44 ml of a 6 mol/L sodium hydroxide aqueous solution, and 250 ml of methanol was heated to reflux for 20 minutes. Thereafter, 30 ml of concentrated hydrochloric acid was added to the reaction mixture solution, and the obtained solution was then concentrated under reduced pressure. Thereafter, the precipitated solid was filtrated, and the obtained solid was then washed with a mixed solvent of hexane and MTBE, so as to obtain 22.3 g of 2-chloro-6-methoxymethylnicotinic acid.
1H-NMR (DMSO-D6) δ: 3.51 (3H, s), 4.62 (2H, s), 7.54 (1H, d, J=7.8 Hz), 8.38 (1H, d, J=7.8 Hz).
3.5 ml of bromine was added to a mixture of 5.11 g of 2-amino-5-fluoropyridine and 20 ml of acetic acid, and the obtained mixture was stirred at 80° C. for 30 minutes.
Thereafter, a saturated sodium bisulfite aqueous solution and a saturated sodium bicarbonate aqueous solution were added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 6.07 g of 2-amino-3-bromo-5-fluoropyridine.
1H-NMR (CDCl3) δ: 4.80 (2H, br s), 7.50 (1H, dd, J=7.5, 2.4 Hz), 7.93 (1H, d, J=2.4 Hz).
0.59 g of copper(I) cyanide was added to a mixture of 1.04 g of the 2-amino-3-bromo-5-fluoropyridine and 20 ml of N-methyl-2-pyrrolidone, and the obtained mixture was stirred at 150° C. for 5 hours. Thereafter, 28% aqueous ammonia was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.52 g of 2-amino-3-cyano-5-fluoropyridine.
1H-NMR (CDCl3) δ: 5.10 (2H, br s), 7.45 (1H, dd, J=7.4, 3.0 Hz), 8.16 (1H, d, J=3.0 Hz).
12.3 ml of N,N-diisopropylamine was mixed with 100 ml of THF. Thereafter, 50 ml of a hexane solution containing 1.6 mol/liter n-butyllithium was mixed therewith at −78° C. The obtained mixture was stirred at −78° C. for 20 minutes. Thereafter, 10.1 g of 2,6-difluoropyridine dissolved in 50 ml of THF was added to the reaction mixture at −78° C. over 10 minutes. The obtained mixture was stirred for 30 minutes. Thereafter, dry ice was added to the reaction mixture, and the obtained mixture was stirred for 4 hours, while the temperature thereof was gradually raised to a room temperature. Thereafter, water was added to the reaction mixture, followed by partition with MTBE. Subsequently, concentrated hydrochloric acid was added to the water layer, so that the pH thereof was adjusted to pH 1, followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over sodium sulfate, followed by concentration under reduced pressure. The obtained residue was washed with a mixed solvent of hexane and MTBE, so as to obtain 8.69 g of 2,6-difluoronicotinic acid.
1H-NMR (DMSO-D6) δ: 7.30 (1H, dd, J=8.2, 2.4 Hz), 8.59 (1H, dd, J=8.2, 4.1 Hz).
A mixture of 11 g of 3-iodophenol, 5.5 g of 3-fluorobenzonitrile and 100 ml of DMF was stirred at 120° C. for 5 hours. Thereafter, water was added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was successively washed with a 5% sodium hydroxide aqueous solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure, so as to obtain 17 g of 3-(3-iodophenyloxy)benzonitrile.
100 ml of a borane-THF-complex-containing THF solution (1 M) was added dropwise to the mixture of 17 g of the obtained 3-(3-iodophenyloxy)benzonitrile and 100 ml of THF. The obtained mixture was stirred under heating to reflux for 8 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and 5% hydrochloric acid was then added the reaction mixture. The obtained mixture was further heated to reflux for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure. Thereafter, water was added to the resultant, 27% sodium hydroxide aqueous solution was added thereto, so that the pH thereof became 13 or more, followed by extraction with chloroform. The chloroform layer was dried over anhydrous potassium carbonate, so as to obtain 14 g of [3-(3-iodophenyloxy)phenyl]methylamine.
A mixture of 7 g of the obtained [3-(3-iodophenyloxy)phenyl]methylamine, 11 g of di-tertiary butyl dicarbonate, 9 ml of triethylamine, 0.1 g of dimethylaminopyridine and 200 ml of THF was stirred at a room temperature for 8 hours. Thereafter, water was added to the reaction mixture, and the obtained mixture was then extracted with MTBE. The organic layer was successively washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column purification, so as to obtain 6.0 g of N-[3-(3-iodophenyloxy)phenyl]methylcarbamic acid tertiary butyl ester.
1H-NMR (CDCl3) δ: 1.45 (9H, s), 4.31 (2H, d, J=5.1 Hz), 4.85 (1H, s), 6.88-6.97 (3H, m), 7.04-7.06 (2H, m), 7.28-7.34 (2H, m), 7.43 (1H, dd, J=7.8, 1.0 Hz).
A mixture of 7.0 g of N-[3-(3-iodophenyloxy)phenyl]methylcarbamic acid tertiary butyl ester, 0.16 g of copper iodide, 4.9 g of trimethylsilylacetylene, 0.95 g of tetrakis(triphenylphosphine)paradium(0), 4.6 ml of triethylamine and 50 ml of DMF was stirred at 90° C. for 6 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, water was added to the reaction mixture, and the obtained mixture was then extracted with MTBE. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column purification, so as to obtain 6 g of N-[3-(3-trimethylsilylethynylphenyloxy)phenyl]methylcarbamic acid tertiary butyl ester.
1H-NMR (CDCl3) δ: 0.23 (9H, s), 1.45 (9H, s), 4.30 (2H, d, J=5.3 Hz), 4.83 (1H, s), 6.87-6.91 (2H, m), 6.96-6.98 (1H, m), 7.03-7.07 (2H, m), 7.19-7.31 (3H, m).
A mixture of 5.8 g of N-[3-(3-trimethylsilylethynylphenyloxy)phenyl]methylcarbamic acid tertiary butyl ester, 4.1 g of potassium carbonate and 70 ml of methanol was stirred at a room temperature for 2 hours. Thereafter, MTBE was added to the reaction mixture, and the obtained mixture was filtrated. The filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column purification, so as to obtain 4.6 g of N-[3-(3-ethynylphenyloxy)phenyl]methylcarbamic acid tertiary butyl ester.
A mixture of 4.4 g of N-[3-(3-ethynylphenyloxy)phenyl]methylcarbamic acid tertiary butyl ester, 4.4 ml of trifluoroacetic acid and 40 ml of chloroform was stirred at 50° C. for 8 hours. Thereafter, the reaction mixture was left to cool around room temperature, followed by concentration under reduced pressure. 10 ml of ethanol and 1.5 ml of 36% hydrochloric acid were added to the obtained residue, followed by concentration under reduced pressure. The obtained crystal was washed with hexane, and it was then dried, so as to obtain 2.3 g of 3-(3-ethynylphenyloxy)benzylamine hydrochloride.
1H-NMR (DMSO-D6) δ: 4.02-4.05 (2H, m), 4.27 (1H, s), 7.03-7.10 (3H, m), 7.21-7.30 (3H, m), 7.40-7.48 (2H, m), 8.33 (3H, s).
A mixture of 5.4 g of 3-fluorobenzonitrile, 5.8 g of 3-methoxyphenol, 15.9 g of cesium carbonate and 30 ml of DMF was stirred at 140° C. for 3 hours. Thereafter the reaction mixture was left to cool to around room temperature. Thereafter, water was added to the reaction mixture, and the obtained mixture was then extracted with ethyl acetate. The organic layer was successively washed with a 15% sodium hydroxide aqueous solution, diluted hydrochloric acid and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 1.1 g of 3-(3-methoxyphenyloxy)benzonitrile.
1H-NMR (CDCl3) δ: 3.80 (3H, s), 6.58-6.61 (2H, m), 6.75 (1H, ddd, J=8.4, 2.4, 0.8 Hz), 7.23-7.44 (5H, m).
0.61 g of 3-fluorobenzonitrile, 0.91 g of 3-butoxyphenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 8 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1.09 g of 3-(4-butoxyphenyloxy)benzonitrile.
0.41 g of 3-(3-butoxyphenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.39 g of 3-(3-butoxyphenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 0.96 (3H, t, J=7.5 Hz), 1.39 (2H, br s), 1.45-1.49 (2H, m), 1.71-1.78 (2H, m), 3.85 (2H, s), 3.92 (2H, t, J=6.4 Hz), 6.56-6.58 (2H, m), 6.63-6.66 (1H, m), 6.90 (1H, d, J=7.6 Hz), 6.98 (1H, s), 7.05 (1H, d, J=7.6 Hz), 7.19-7.22 (1H, m), 7.29 (1H, t, J=7.8 Hz).
0.61 g of 3-fluorobenzonitrile, 0.89 g of 2-trifluoromethylphenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.43 g of 3-(2-trifluoromethylphenyloxy)benzonitrile.
0.40 g of 3-(2-trifluoromethylphenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.32 g of 3-(2-trifluoromethylphenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.78 (2H, br s), 3.88 (2H, s), 6.94-6.96 (2H, m), 7.03-7.08 (4H, m), 7.28-7.30 (2H, m).
0.61 g of 3-fluorobenzonitrile, 0.62 g of 4-fluorophenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.92 g of 3-(4-fluorophenyloxy)benzonitrile.
0.32 g of 3-(4-fluorophenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.31 g of 3-(4-fluorophenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.51 (2H, br s), 3.85 (2H, s), 6.84 (1H, dd, J=8.2, 4.1 Hz), 6.93-7.06 (6H, m), 7.27-7.30 (1H, m).
0.61 g of 3-fluorobenzonitrile, 0.62 g of 3-fluorophenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 0.86 g of 3-(3-fluorophenyloxy)benzonitrile.
0.33 g of 3-(3-fluorophenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.30 g of 3-(3-fluorophenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.86 (2H, d, J=5.1 Hz), 6.69 (1H, m), 6.78-6.80 (2H, m), 6.91 (1H, dd, J=8.1, 2.3 Hz), 7.01 (1H, s), 7.10 (1H, d, J=7.6 Hz), 7.24-7.34 (2H, m).
0.61 g of 3-fluorobenzonitrile, 0.70 g of 4-chlorophenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1.00 g of 3-(4-chlorophenyloxy)benzonitrile.
0.34 g of 3-(4-chlorophenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.34 g of 3-(4-chlorophenyloxy)benzylamine. 3-(4-chlorophenyloxy)benzylamine
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.86 (2H, s), 6.86-6.88 (1H, m), 6.92-6.96 (3H, m), 7.07 (1H, d, J=7.6 Hz), 7.28-7.32 (3H, m).
0.61 g of 3-fluorobenzonitrile, 0.89 g of 2-trifluoromethylphenol and 1.95 g of cesium carbonate were added to 5 ml of DMF. The obtained mixture was heated to reflux for 20 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, diluted hydrochloric acid was added to the reaction mixture, and it was then extracted with diethyl ether. The organic layer was successively washed with a sodium hydroxide aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate. The resultant was concentrated by centrifugation under reduced pressure, so as to obtain 1.10 g of 3-(3-trifluoromethylphenyloxy)benzonitrile.
0.40 g of 3-(3-trifluoromethylphenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The mixture solution was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.32 g of 3-(3-trifluoromethylphenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.43 (2H, br s), 3.88 (2H, s), 6.90 (1H, dd, J=8.1, 2.0 Hz), 7.01 (1H, s), 7.13-7.16 (2H, m), 7.24 (1H, s), 7.32-7.36 (2H, m), 7.43-7.45 (1H, m).
12.3 ml of N,N-diisopropylamine was mixed with 100 ml of THF. Thereafter, 50 ml of a hexane solution containing 1.6 mol/liter n-butyllithium was mixed therewith at −78° C. The obtained mixture was stirred at −78° C. for 20 minutes. Thereafter, 10.1 g of 2,6-difluoropyridine dissolved in 50 ml of THF was added to the reaction mixture at −78° C. over 10 minutes. The obtained mixture was stirred for 30 minutes. Thereafter, dry ice was added to the reaction mixture, and the obtained mixture was stirred for 4 hours, while the temperature thereof was gradually raised to a room temperature. Thereafter, water was added to the reaction mixture, followed by partition with MTBE. Subsequently, concentrated hydrochloric acid was added to the water layer, so that the pH thereof was adjusted to pH 1, followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over sodium sulfate, followed by concentration under reduced pressure. The obtained residue was washed with a mixed solvent of hexane and MTBE, so as to obtain 8.69 g of 2,6-difluoronicotinic acid.
1H-NMR (DMSO-D6) δ: 7.30 (1H, dd, J=8.2, 2.4 Hz), 8.59 (1H, dd, J=8.2, 4.1 Hz).
0.45 g of 4-(2-chloro-4-trifluoromethylphenyloxy)benzonitrile was added to 1 ml of THF. 1 ml of a THF solution of lithium aluminum hydride (2.0 M) was added dropwise to the mixture solution at 0° C., and the obtained mixture was stirred at a room temperature for 3 hours. Thereafter, 1 ml of ethanol, 1 ml of water, and 1 ml of a 15% sodium hydroxide aqueous solution were successively added dropwise to the reaction mixture at 0° C. The reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated by centrifugation under reduced pressure, so as to obtain 0.36 g of 4-(2-chloro-4-trifluoromethylphenyloxy)benzylamine.
1H-NMR (CDCl3) δ: 1.52 (2H, br s), 3.89 (2H, s), 6.96-7.04 (2H, m), 7.30-7.36 (2H, m), 7.41-7.43 (1H, m), 7.56-7.58 (1H, m), 7.73 (1H, d, J=2.0 Hz).
A mixture solution of 10 g of 2-fluoro-3-methoxybenzaldehyde and 80 ml of ethanol was added to a mixture solution of 1.8 g of 10% palladium on carbon, 10 ml of water, 6.5 ml of 10N hydrochloric acid and 50 ml of ethanol. Thereafter, 5.4 g of hydroxylamine hydrochloride was added to the mixture. The obtained mixture was stirred at a room temperature for 2 hours. The mixture was stirred at a room temperature under a hydrogen atmosphere at about 1 atm for 3 hours. Thereafter, the reaction mixture was filtrated through Celite (registered trade mark), and the filtrate was then concentrated under reduced pressure. Thereafter, water was added to the residue, followed by extraction with chloroform. 15% sodium hydroxide aqueous solution was added to the extract until the pH of the obtained water layer was adjusted to pH 11, followed by extraction with chloroform. The organic layer was dried over potassium carbonate, followed by concentration under reduced pressure, so as to obtain 8.0 g of 2-fluoro-3-methoxybenzylamine.
1H-NMR (CDCl3) δ: 1.55 (2H, br s), 3.89 (3H, s), 3.90 (2H, br s), 6.86-6.91 (2H, m), 7.02-7.06 (1H, m).
15 ml of 48% hydrobromic acid was added to 4 g of 2-fluoro-3-methoxybenzylamine hydrochloride. The obtained mixture was heated to reflux for 5 hours. Thereafter, the reaction mixture was left to cool to around room temperature, and it was then concentrated under reduced pressure, so as to obtain 4.0 g of 2-fluoro-3-hydroxybenzylamine hydrobromide.
1H-NMR (DMSO-d6) δ: 4.04 (2H, q, J=5.5 Hz), 6.90-6.94 (1H, m), 6.97-7.06 (2H, m), 8.23 (3H, br s), 10.05 (1H, br s).
A mixture of 26 g of 2-fluoro-3-hydroxybenzylamine hydrobromide, 49 g of di-tert-butyl dicarbonate, 64 ml of triethylamine, about 0.1 g of 4-dimethylaminopyridine and 300 ml of tetrahydrofuran was stirred at a room temperature for 6 hours. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with 5% hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure, so as to obtain about 20 g of [2-fluoro-3-(4-hydroxy)phenyl]methylcarbamic acid 1,1-dimethylethyl.
A mixture of about 20 g of the thus obtained [2-fluoro-3-(4-hydroxy)phenyl]methylcarbamic acid 1,1-dimethylethyl, 11 g of 5-chloro-1-pentyne, 44 g of cesium carbonate and 200 ml of DMF was stirred at 80° C. for 4 hours, and then at 100° C. for 2 hours. Thereafter, the reaction mixture was left to cool to around room temperature. Thereafter, water was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was successively washed with 3% sodium hydroxide solution, 5% hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and a saturated saline solution, and it was then dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 18g of [2-fluoro-3-(4-pentynyloxy)phenyl]methylcarbamic acid 1,1-dimethylethyl.
1H-NMR (CDCl3) δ: 1.45 (9H, s), 1.97 (1H, t, J=2.7 Hz), 2.00-2.06 (2H, m), 2.43 (2H, td, J=7.0, 2.7 Hz), 4.13 (2H, t, J=6.1 Hz), 4.35-4.37 (2H, m), 4.88 (1H, s), 6.89-6.92 (1H, m), 6.99-7.03 (1H, m), 7.07-7.14 (1H, m).
17 g of [2-fluoro-3-(4-pentynyloxy)phenyl]methylcarbamic acid 1,1-dimethylethyl was mixed with 17 ml of trifluoroacetic acid and 50 ml of chloroform at a room temperature for 5 hours. The obtained reaction mixture was concentrated under reduced pressure. Thereafter, a mixture of 100 ml of ethanol and 6 ml of acetyl chloride was added to the residue, followed by concentration under reduced pressure, so as to obtain 8.7 g of [2-fluoro-3-(4-pentynyloxy)phenyl]methylamine hydrochloride.
1H -NMR (DMSO-D6) δ: 1.88-1.95 (2H, m), 2.34 (2H, td, J=7.0, 2.6 Hz), 2.84 (1H, dd, J=2.7, 1.9 Hz), 4.01-4.04 (2H, m), 4.13 (2H, t, J=6.0 Hz), 7.12-7.24 (3H, m), 8.51 (3H, s).
8.0 g of triethylamine was added to a mixture of 7.0 g of 2-fluoro-3-hydroxybenzylamine hydrobromide and 70 ml of DMF. Subsequently, 7.7 g of 2-aminonicotinic acid was added thereto, and 18.1 g of a BOP reagent was further added thereto. The obtained mixture was stirred at a room temperature for 10 hours. Thereafter, 30 ml of pyridine was added to the reaction mixture, and the obtained mixture was stirred at 110° C. for 3 hours. Thereafter, the reaction mixture was cooled to a room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was successively washed with a saturated sodium bicarbonate solution, water and a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was washed with hexane and MTBE, so as to obtain 5.4 g of N-(2-fluoro-3-hydroxyphenylmethyl)-2-aminonicotinic acid amide.
1H-NMR (DMSO-D6) δ: 4.44 (2H, d, J=5.6 Hz), 6.59 (1H, dd, J=7.7, 4.8 Hz), 6.71-6.75 (1H, m), 6.84 (1H, td, J=8.2, 1.7 Hz), 6.90-6.94 (1H, m), 7.06 (2H, br s), 7.95 (1H, dd, J=7.7, 1.9 Hz), 8.08 (1H, dd, J=4.7, 1.8 Hz), 8.91 (1H, t, J=5.8 Hz), 9.77 (1H, s).
Next, formulation examples will be given below. It is to be noted that the term “part” indicates “part by weight.”
50 parts of each of the present compounds 1 to 347, 3 parts of calcium lignosulfonate, 2 parts of magnesium lauryl sulfate, and 45 parts of synthetic hydrous silicon oxide were fully crushed and mixed, so as to obtain various types of wettable powders.
20 parts of each of the present compounds 1 to 347 and 1.5 parts of sorbitan trioleate were mixed into 28.5 parts of an aqueous solution that contained 2 parts of polyvinyl alcohol, and the mixture solution was then subjected to fine grinding according to a wet grinding method. Thereafter, 40 parts of an aqueous solution that contained 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate was added to the resultant, and 10 parts of propylene glycol was further added thereto. The obtained mixture was blended by stirring, so as to obtain various types of flowable formulations.
2 parts of each of the present compounds 1 to 347, 88 parts of kaoline clay, and 10 parts of talc were fully crushed and mixed, so as to obtain various types of powder products.
5 parts of each of the present compounds 1 to 347, 14 parts of polyoxyethylene styryl phenyl ether, 6 parts of calcium dodecylbenzenesulfonate, and 75 parts of xylene were fully mixed, so as to obtain various types of emulsions.
2 parts of each of the present compounds 1 to 347, 1 part of synthetic hydrous silicon oxide, 2 parts of calcium lignosulfonate, 30 parts of bentonite, and 65 parts of kaoline clay were fully crushed and mixed. Thereafter, water was added to the mixture, and they were fully blended, followed by granulation and drying, so as to obtain various types of granules.
10 parts of each of the present compounds 1 to 347, 35 parts of white carbon that contained 50 parts of polyoxyethylene alkyl ether sulfate ammonium salts, and 55 parts of water were mixed, and the obtained mixture was then subjected to fine grinding according to a wet grinding method, so as to obtain various types of formulations.
Next, test examples will be given to demonstrate that the present invention is useful for the control of plant diseases.
Such control effect was evaluated by visually observing the area of blotch on a test plant during a test and then comparing the area of the blotch of a plant treated with the controlling reagent of the present invention with the area of the blotch of an untreated plant.
A plastic pot was filled with sandy soil, and cucumber (variety: Sagami-Hanjiro) was then seeded. The cucumber was allowed to grow in a green house for 12 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned cucumber plants. After completion of the foliage application, the plants were air-dried. Thereafter, the spores of the pathogenic microbes were applied onto the plant leaf surface. After such inoculation, the plants were left in a green house at 23° C. for 10 days. Thereafter, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
7, 10, 11, 20, 23, 24, 26, 27, 28, 29, 31, 38, 46, 48, 49, 50, 51, 52, 58, 62, 72, 73, 74, 80, 82, 85, 86, 90, 91, 92, 97, 98, 100, 102, 103, 108, 109, 112, 115, 116, 122, 123, 125, 126, 127, 128, 131, 132, 133, 134, 135, 136, 137, 141, 143, 145, 147, 155, 156, 157, 159, 160, 161, 162, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 181, 183, 188, 189, 191, 193, 194, 195, 199, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 219, 220, 221, 222, 224, 225, 226, 227, 228, 231, 232, 233, 235, 238, 243, 247, 248, 255, 263, 264, 265, 267, 272, 278, 279, 280, 283, 284, 286, 287, 297, 298, 300, 301, 302, 304, 305, 305, 306, 307, 308, 309, 312, 314, 315, 318, 319, 320, 321, 322, 323, 344, and 347.
A plastic pot was filled with sandy soil, and wheat (variety: Apogee) was then seeded. The wheat was allowed to grow in a green house for 10 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned wheat plants. After completion of the foliage application, the plants were air-dried. Two days later, a water suspension containing the wheat leaf blight spores was inoculated into the cotyledona surface by spraying it. After such inoculation, the plants were left at 23° C. at a high humidity for 3 days, and then under illumination for 14 to 18 days. Thereafter, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants. 20, 29, 54, 62, 92, 115, 122, 127, 134, 175, 176, 179, 183, 185, 203, 204, 205, 206, 208, 211, 212, 213, 229, 238, 247, 249, 252, 260, 265, 266, 268, 269, 272, 273, 275, 276, 282, 284, 287, 297, 298, 300, 302, 304, 305, 307, 308, 309, 313, 343, and 344.
A plastic pot was filled with sandy soil, and cucumber (variety: Sagami-Hanjiro) was then seeded. The cucumber was allowed to grow in a green house for 12 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned cucumber plants. After completion of the foliage application, the plants were air-dried. Thereafter, a Botrytis cinerea spore-containing PDA medium was placed on the plant leaf surface. After such inoculation, the plants were left at 12° C. at a high humidity for 4 days. Thereafter, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
3, 11, 16, 17, 19, 20, 21, 22, 23, 28, 29, 31, 34, 35, 37, 38, 39, 40, 46, 48, 54, 55, 57, 59, 61, 62, 77, 82, 83, 84, 87, 90, 92, 94, 95, 96, 98, 100, 112, 115, 116, 118, 119, 122, 126, 132, 135, 149, 152, 171, 173, 175, 176, 178, 179, 180, 181, 182, 183, 188, 190, 191, 198, 199, 210, 218, 225, 227, 236, 240, 241, 242, 244, 245, 246, 249, 250, 251, 255, 257, 258, 259, 260, 261, 262, 263, 280, 282, 286, 308, 309, 314, 315, 318, 319, 320, 321, 323, 346, and 347.
A plastic pot was filled with sandy soil, and cucumber (variety: Sagami-Hanjiro) was then seeded. The cucumber was allowed to grow in a green house for 12 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned cucumber plants. After completion of the foliage application, the plants were air-dried. Thereafter, a cucumber Sclerotinia sclerotiorum hypha-containing PDA medium was placed on the cucumber leaf surface. After such inoculation, the plants were left at 18° C. at a high humidity for 4 days. Thereafter, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
3, 7, 8, 10, 11, 14, 16, 17, 18, 19, 20, 21, 23, 25, 27, 28, 29, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 43, 46, 47, 48, 49, 51, 52, 53, 54, 55, 57, 58, 59, 60, 61, 62, 65, 66, 67, 68, 73, 77, 78, 79, 80, 82, 83, 84, 86, 87, 88, 89, 90, 92, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 106, 107, 109, 110, 111, 112, 113, 115, 116, 117, 118, 119, 122, 123, 124, 126, 127, 128, 131, 132, 133, 134, 135, 139, 141, 142, 145, 149, 150, 151, 152, 153, 154, 164, 165, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 186, 188, 190, 191, 194, 195, 196, 197, 198, 199, 200, 202, 203, 205, 206, 208, 209, 210, 211, 212, 215, 218, 219, 221, 222, 224, 225, 226, 227, 228, 232, 233, 235, 236, 240, 241, 242, 243, 244, 245, 246, 248, 249, 250, 251, 254, 262, 263, 264, 266, 314, 315, and 343.
A plastic pot was filled with sandy soil, and Japanese radish (variety: Wase-Shijunichi) was then seeded. The Japanese radish was allowed to grow in a green house for 5 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned Japanese radish plants. After completion of the foliage application, the plants were air-dried. Thereafter, a water suspension containing the Japanese radish black spot spores was sprayed onto the plant leaf surface. After such inoculation, the plants were first left at 24° C. at a high humidity for 1 day, and then in a green house for 3 days. Thereafter, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
5, 10, 11, 27, 29, 48, 50, 51, 52, 72, 73, 74, 102, 122, 133, 134, 137, 139, 145, 149, 156, 159, 161, 162, 167, 168, 169, 170, 172, 175, 176, 178, 179, 183, 187, 188, 189, 191, 193, 194, 195, 199, 200, 206, 207, 208, 210, 213, 214, 216, 219, 227, 231, 232, 233, 247, and 249.
A plastic pot was filled with sandy soil, and grape (variety: Berry-A or Chardonnay seedling) was then seeded. The grape plants were allowed to grow in a green house for 40 days. A water suspension of zoosporangium of grape Plasmopara viticola was inoculated to the aforementioned pot by spaying it. Thereafter, the grape plants were left at 23° C. at a high humidity for 1 day, and they were then air-dried, so as to obtain grape downy mildew-infected nursery plants. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned nursery grape plants. After completion of the foliage application, the plants were subjected to air-drying, and they were then left at 23° C. in a green house for 5 days. Thereafter, the plants were further left at 23° C. at a high humidity for 1 day. Thereafter, the affected areas thereof were examined. As a result, it was found that the affected areas of plants which had been treated with the present compound 236 were 30% or less of the affected areas of untreated plants.
A plastic pot was filled with sandy soil, and tomato (variety: Patio) was then seeded. The tomato was allowed to grow in a green house for 20 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned nursery tomato plants. The plants were subjected to air-drying to such an extent that the diluted solution on the leave surface could be dried. Thereafter, a Phytophthora infestans spore-containing water suspension was inoculated into the nursery tomato plants by spraying it. After completion of the inoculation, the plants were first left at 23° C. at a high humidity for 1 day, and they were then allowed to grow in a green house for 4 days. Thereafter, the affected areas thereof were examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds were 30% or less of the affected areas of untreated plants.
1, 2, 8, 9, 10, 11, 12, 13, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 29, 31, 32, 34, 35, 39, 41, 43, 44, 48, 49, 51, 52, 64, 71, 75, 85, 86, 89, 90, 92, 95, 96, 97, 98, 102, 103, 104, 105, 106, 108, 110, 119, 124, 133, 134, 135, 138, 139, 140, 141, 143, 144, 146, 147, 148, 149, 152, 153, 156, 157, 158, 159, 160, 161, 162, 163, 173, 176, 183, 184, 186, 187, 188, 189, 190, 191, 193, 199, 201, 202, 203, 208, 209, 212, 213, 216, 224, 230, 247, 248, 253, 256, 257, 283, 296, 297, 298, 300, 301, 302, 305, 307, 310, 311, 312, 315, 317, 319, 321, 323, 343, 346, and 347.
A plastic pot was filled with soil, and rice (variety: Nihonbare) was then seeded. The rice plants were allowed to grow in a green house for 12 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned rice plants. After completion of the foliage application, the plants were subjected to air-drying. Thereafter, pots containing leaves infected with rice blast disease were left at rest around the applied rice plants. All the rice plants were left at a high humidity only during the night. Five days after the inoculation, the affected areas thereof were examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
3, 8, 11, 17, 18, 19, 20, 21, 23, 28, 29, 31, 34, 35, 36, 37, 39, 40, 41, 44, 46, 47, 48, 49, 51, 52, 53, 58, 59, 61, 62, 69, 71, 72, 73, 74, 76, 77, 79, 82, 90, 91, 92, 93, 94, 95, 96, 97, 104, 112, 113, 115, 116, 118, 119, 122, 126, 127, 128, 130, 132, 135, 136, 138, 140, 141, 142, 143, 165, 166, 167, 168, 171, 172, 173, 174, 175, 176, 177, 179, 180, 181, 182, 183, 188, 189, 193, 194, 195, 196, 199, 200, 201, 202, 203, 205, 206, 207, 208, 209, 210, 211, 212, 218, 219, 221, 224, 225, 228, 229, 232, 233, 234, 235, 236, 237, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 255, 256, 257, 258, 259, 260, 261, 263, 365, 266, 268, 269, 271, 273, 279, 280, 282, 293, 284, 285, 286, 297, 298, 300, 301, 311, 312, 314, 315, 318, 319, 320, 343, 344, 345, 346, and 347.
A plastic pot was filled with sandy soil, and wheat (variety: Shirogane) was then seeded. The wheat was allowed to grow in a green house for 10 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned wheat plants. Five days later, spores of wheat brown leaf rust microbes were inoculated into the wheat plants by spraying it. After completion of the inoculation, the plants were first left at 18° C. at a high humidity in a dark place for 1 day, and they were then left under illumination for 9 days. Thereafter, the affected areas thereof were examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
70, 115, 117, 122, 127, 134, 157, 176, 178, 179, 183, 188, 203, 205, 206, 207, 208, 212, 213, 214, 215, 216, 219, 229, 239, 247, 248, 249, 269, 271, 273, 298, 305, 309, and 317.
A plastic pot was filled with soil contaminated with tomato wilt (Fusarium oxysporum), and tomato (variety: Patio) was then seeded. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were then diluted with water. Thereafter, the aforementioned solution was applied to the soil by a soil drench treatment, such that 10 mg of the present compound could be applied to each plastic pot. The tomato plants were then allowed to grow in a green house for 1 month. Thereafter, the growing condition of the plants was examined. As a result, it could be confirmed that when compared with plants grown in soil that had not been subjected to a soil drench treatment with the present compounds 1 to 347 (untreated group), plants grown in soil treated with the present compounds 1 to 347 (treated group) had reduced tomato wilt symptoms.
A plastic pot was filled with soil contaminated with potato blue stem (Verticillium albo-atrum, V. dahliae, V. nigrescens), and potato (variety: Danshaku) was then planted. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were then diluted with water. Thereafter, the aforementioned solution was applied to the soil by a soil drench treatment, such that 10 mg of the present compound could be applied to each plastic pot. The potato plants were then allowed to grow in a green house for 2 months. Thereafter, the growing condition of the plants was examined. As a result, it could be confirmed that when compared with plants grown in soil that had not been subjected to a soil drench treatment with the present compounds 1 to 347 (untreated group), plants grown in soil treated with the present compounds 1 to 347 (treated group) had reduced potato blue stem symptoms.
Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared formulations were diluted with water to 2000 ppm. Thereafter, unhulled rice contaminated with rice bakanae disease (Gibberella fujikuroi) was subjected to a seed treatment by an immersion method. Thereafter, the aforementioned contaminated unhulled rice that had been subjected to the seed treatment was seeded in a nursery box filled with soil, and it was then allowed to grow in a green house for 1 month. Thereafter, the growing condition of the plants was examined. As a result, it could be confirmed that when compared with plants that had not been subjected to a seed treatment with the present compounds 1 to 347 (untreated group), plants subjected to such a seed treatment with the present compounds 1 to 347 (treated group) had reduced rice bakanae disease symptoms.
Flowable formulations were produced from the present compounds in accordance with Formulation example 6. Thereafter, wheat seeds contaminated with malt damping off (Gaeumannomyces graminis) were subjected to a seed treatment by a smear method with a seed dresser. That is, they were treated with the aforementioned flowable formulations, such that 200 g of the present compound could be applied to 100 kg of the contaminated seeds. Thereafter, the aforementioned contaminated seeds that had been subjected to the seed treatment were seeded in a plastic pot filled with sandy soil, and they were then allowed to grow in a green house for 1 month. Thereafter, the growing condition of the plants was examined. As a result, it could be confirmed that when compared with plants that had not been subjected to a seed treatment with the present compounds 1 to 347 (untreated group), plants subjected to such a seed treatment with the present compounds 1 to 347 (treated group) had reduced malt damping off symptoms.
A plastic pot was filled with sandy soil, and kidney beans (variety: Nagauzura) were then seeded. The kidney bean plants were allowed to grow in a green house for 8 days. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned kidney bean plants. After completion of the foliage application, the plants were air-dried. Thereafter, a kidney bean Sclerotinia sclerotiorum hypha-containing PDA medium was placed on the kidney bean leaf surface. After such inoculation, all the kidney bean plants were left at a high humidity only during the night. Five days after the inoculation, the affected areas thereof were then examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds as indicated below were 30% or less of the affected areas of untreated plants.
255, 256, 257, 267, 269, 282, 296, 297, 298, 301, 304, 305, 309, 320, 322, 344, 345, and 346.
A plastic pot was filled with sandy soil, and cucumber (variety:Sagami-Hanjiro) was then seeded. The cucumber plants were allowed to grow in a green house for 12 days. A water suspension of zoosporangium of cucumber Pseudoperonospora cubensis was inoculated to the aforementioned pot by spraying it. Thereafter, the cucumber plants were left at 23° C. at a high humidity for 1 day, and they were then air-dried, so as to obtain cucumber downy mildew-infected nursery plants. Flowable formulations were produced from the present compounds in accordance with Formulation example 6. The prepared flowable formulations were set to a predetermined concentration (500 ppm) by diluting them with water, and they were then subjected to foliage application such that they could be sufficiently attached to the leaves of the aforementioned nursery cucumber plants. After completion of the foliage application, the plants were subjected to air-drying, and they were then left at 23° C. in a green house for 5 days. Thereafter, the plants were further left at 23° C. at a high humidity for 1 day. Thereafter, the affected areas thereof were examined. As a result, it was found that the affected areas of plants which had been treated with the present compounds 298, 300, 305, 309, 318, 319, 320, 321, 323, 346 and 347 were 30% or less of the affected areas of untreated plants.
According to the present invention, plant diseases caused by plant pathogenic microbes (except for Aspergillus) can be controlled or prevented.
Number | Date | Country | Kind |
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2008-045846 | Feb 2008 | JP | national |
2008-224469 | Sep 2008 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2009/053646 | 2/27/2009 | WO | 00 | 8/25/2010 |