发明名称 Cyclic amide derivative
摘要 [Problem];To provide a GPR40 activating agent having, as an active ingredient, a novel compound having a GPR40 agonist action, a salt of the compound, a solvate of the salt or the compound, or the like, particularly, an insulin secretagogues and a prophylactic and/or therapeutic agent against diabetes, obesity, or the like.;[Means of solving the problem];A compound of Formula (III):;(where f is 0 to 2; g is 1 to 4; j is 0 to 3; k is 0 to 2; n is 0 to 2; p is 0 to 4; h is 0 to 3; q1 id 0 to 3; q2 is 0 or 1; r1 is 0 to 2 (with the proviso that q1+q2+r1 is 0 to 5); J1a is —CR11a—, N; J2 is —CR12aR12b—, —CR12c—; T is —CH2—, O, —S(O)i— (i is an integer of 0 to 2) or —NR7—; X is O, S, or —NR7—; ring A′″ is a benzene ring, a pyridine ring; ring B′ is a benzene ring, a pyridine ring, a pyrimidine ring; and R1 to R14 are specific groups),a salt of the compound, or a solvate of the salt or the compound.
申请公布号 US9072758(B2) 申请公布日期 2015.07.07
申请号 US201214114017 申请日期 2012.04.11
申请人 MOCHIDA PHARMACEUTICAL CO., LTD. 发明人 Okano Akihiro;Ohkouchi Munetaka;Makabe Muneyoshi
分类号 C07D279/02;C07D285/10;C07D285/16;C07D417/12;C07D417/14;A61K31/69;A61K31/425;A61K31/4439;A61K31/54;A61K31/541;A61K31/549;A61K45/06;C07D275/03;C07F5/04;A61K9/14;A61K9/16;A61K9/20;A61K9/48 主分类号 C07D279/02
代理机构 Birch, Stewart, Kolasch & Birch, LLP 代理人 Birch, Stewart, Kolasch & Birch, LLP
主权项 1. A compound selected from the following compound group: 5-[4-[[3-(2,6-dimethylphenyl)phenyl]methoxy]phenyl]-1,1-dioxo-1,2-thiazinan-3-one; 5-[4-[[3-(2,6-dimethyl-4-(3-methylsulfonylpropoxy)phenyl]phenyl]methoxy]phenyl]-1,1-dioxo-1,2-thiazinan-3-one; 4-(((1R)-1-(4-(1,1-dioxo-3-oxo-1,2-thiazinan-5-yl)phenoxy)-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile; 5-(4-(((R)-4-bromo-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,1-dioxo-1,2-thiazinan-3-one; 5-(4-(((R)-4-(4-(3-hydroxy-3-methylbutoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,1-dioxo-1,2-thiazinan-3-one; 5-[4-[[3-[6-(3-hydroxy-3-methylbutoxy)-2,4-dimethylpyridin-3-yl]phenyl]methoxy]phenyl]-1,1-dioxo-1,2-thiazinan-3-one 5-(4-(((R)-4-(6-(3-hydroxy-3-methylbutoxy)-2-methylpyridin-3-yl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(2-(trifluoromethyl)phenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(4-(2-ethoxyethoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(4-(3-hydroxy-3-methylbutoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(2,6-dimethyl-4-(3-(methylsulfonyl)propoxy)phenyl)-2,3-dihydro1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(4-methoxy-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-(4-(3-hydroxy-3-methylbutoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yl)oxy)-2-methylphenyl)-1,2-thiazinan-3-one 1,1-dioxide; 5-(4-(((R)-4-phenoxy-2,3-dihydro-1H-inden-1-yl)oxy)phenyl)-1,2-thiazinan-3-one 1,1-dioxide;or a pharmaceutically acceptable salt of the compound, an optical isomer of the compound, or a pharmaceutically acceptable salt of the isomer.
地址 Tokyo JP