首页> 外国专利> 6-Benzyl-2H-pyridazin-3-one derivatives,their preparation and their use as inhibitors of prostaglandin G/H synthase I and II (COX I and COX II)

6-Benzyl-2H-pyridazin-3-one derivatives,their preparation and their use as inhibitors of prostaglandin G/H synthase I and II (COX I and COX II)

机译:6-苄基-2H-哒嗪-3-酮衍生物,其制备及其作为前列腺素G / H合酶I和II(COX I和COX II)的抑制剂的用途

摘要

Compounds of formula I: CHEM where: the dashed line denotes an optional bond; R1 is H, halo, alkyl, alkyloxy, amino, alkylamino, dialkylamino, or acylamino; R3 and R4 are independently H, halo, alkyl, alkyloxy, or hydroxy; R5 is H, halo, alkyl, alkylthio, alkyloxy, alkenyloxy, alkynyl, or alkenyl; provided that at least one of R1, R3, R4, and R5 is H; R7 is H, alkyl, cyano, or amido; R10 is a group represented by formula (A), (B), or (C); CHEM where: X is O or S; R12, R13, R15, and R16 are independently H, halo, alkyl, alkyloxy, or alkylthio; and R14 is H, halo, alkyl, alkylthio, alkyloxy, alkenyloxy, alkynyl, alkenyl, or -SO2R17 where R17 is alkyl, or -SO2NR18R19 where R18 and R19 are independently H or alkyl; provided that at least two of R12, R13, R14, R15, and R16 are H, and that if only two of R12, R13, R15, and R16 are H, the non-hydrogen substituents are not all adjacent; and at least one of R12 and R16 is H when neither R1 nor R3 are H; and R20 is H, alkyl, haloalkyl, hydroxyalkyl, or alkenyl; and their pharmaceutically acceptable salts are inhibitors of prostaglandin G/H synthase and are anti-inflammatory and analgesic agents.
机译:式I的化合物:其中:虚线表示任选的键; R1为H,卤素,烷基,烷氧基,氨基,烷基氨基,二烷基氨基或酰基氨基; R3和R4独立地为H,卤素,烷基,烷氧基或羟基; R5为H,卤素,烷基,烷硫基,烷氧基,烯氧基,炔基或烯基;前提是R1,R3,R4和R5中至少一个是H; R7是H,烷基,氰基或酰胺基; R10是由式(A),(B)或(C)表示的基团; 其中:X为O或S; R12,R13,R15和R16独立地为H,卤素,烷基,烷氧基或烷硫基; R14是H,卤素,烷基,烷硫基,烷氧基,烯氧基,炔基,烯基或-SO2R17,其中R17是烷基,或-SO2NR18R19,其中R18和R19独立地是H或烷基;前提是R 12,R 13,R 14,R 15和R 16中的至少两个是H,并且如果R 12,R 13,R 15和R 16中只有两个是H,则非氢取代基不是全部相邻。当R1和R3都不为H时,R12和R16中的至少一个为H; R 20为H,烷基,卤代烷基,羟烷基或烯基;其药学上可接受的盐是前列腺素G / H合酶的抑制剂,是抗炎和镇痛药。

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