首页> 外国专利> AMIDINE DERIVATIVES OF 2-HETEROARIL-QUINAZOLINAS AND QUINOLINAS; POWERFUL ANALGESIC AND ANTI-INFLAMMATORY AGENTS.

AMIDINE DERIVATIVES OF 2-HETEROARIL-QUINAZOLINAS AND QUINOLINAS; POWERFUL ANALGESIC AND ANTI-INFLAMMATORY AGENTS.

机译:2-杂芳基-喹啉和喹啉的亚胺基衍生物;强大的镇痛剂和抗炎剂。

摘要

Compounds of formula (I): ** (See formula) ** in which: - X is independently selected from a carbon atom or a nitrogen atom; - Z and Y are independently selected from an oxygen atom (-O-), a sulfur atom (-S-) or the groups: -CH2-, -CHR2-, -CH =, -CR2 =; - Q is independently selected from the groups: -CH2-, -CHR2-, -CH =, -CR2 =, -CH2-CH2- or -CHR2-CH2-; with the proviso that the combination of the groups Y, Z and Q results in a hexa-atomic or penta-atomic benzo-condensed heterocycle, preferably selected from 1,3-benzodioxol, 1,3-benzodithiol, benzofuran, 2,3- dihydrobenzofuran, benzothiophene, 2,3-dihydrobenzothiophene, 2H-3,4-dihydrobenzopyran, 2H-3,4-dihydrobenzothiopyran, [1,4] -benzodioxine and 2,3-dihydro- [1,4] benzodioxine- (1, 4-benzodioxane); R1 is independently selected from C1-C4 alkyl or C3-C4 cycloalkyl; the C1-C4 alkyl group being a linear or branched, saturated or unsaturated hydrocarbon chain; R2 is independently selected from C1-C4 alkyl and alkoxy (-OR1); the compounds of formula (I) being in the form of a free base or as their pharmaceutically acceptable salt, hydrate or solvate.
机译:式(I)的化合物:**(参见式)**其中:-X独立地选自碳原子或氮原子; -Z和Y独立地选自氧原子(-O-),硫原子(-S-)或-CH 2-,-CHR 2-,-CH =,-CR 2 =; -Q独立地选自:-CH 2-,-CHR 2-,-CH =,-CR 2 =,-CH 2 -CH 2-或-CHR 2 -CH 2-。前提条件是基团Y,Z和Q的组合会产生六原子或五原子苯并稠合的杂环,优选选自1,3-苯并二恶醇,1,3-苯并二硫醇,苯并呋喃,2,3-二氢苯并呋喃,苯并噻吩,2,3-二氢苯并噻吩,2H-3,4-二氢苯并吡喃,2H-3,4-二氢苯并噻喃,[1,4]-苯并二恶英和2,3-二氢-[1,4]苯并二恶英-(1, 4-苯并二恶烷); R1独立地选自C1-C4烷基或C3-C4环烷基; C1-C4烷基为直链或支链的饱和或不饱和烃链; R2独立地选自C1-C4烷基和烷氧基(-OR1);式(I)化合物为游离碱形式或其可药用盐,水合物或溶剂化物。

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