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QUINOLINE AND QUINOXALINE DERIVATIVES EFFECTIVE AS CYSTEINYL-LEUKOTRIENE ANTAGONISTS

机译:喹啉和喹喔啉衍生物可作为半胱氨酸-白三烯类拮抗剂

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to organic chemistry, specifically to a heterocyclic compound of formula (IA) or to a pharmaceutically acceptable salt thereof, where in each case R1 and R3 are independently selected from a group comprising hydrogen, halogen, -OH, -C1-2alkyl, -O-C1-2alkyl, -O-C1halogenalkoxy, -N(C1alkyl)2; R2 represents hydrogen; W represents a group selected from -CH= or -N=; X represents a group selected from -CH=CH- or -N=CH-, where nitrogen from -N=CH- is directly bonded with ring 'a'; Y represents a group selected from -CH=CH- or -C≡C-; Z denotes a bond or group selected from -(CH2)n- and -CH=CH-; A is a group selected from -OR, -O(CH2)nphenyl, -O(CH2)nthiophene; P is selected from a group comprising -O-; Q is a group selected from -COOH; where R is selected from a group comprising hydrogen, -C1-6alkyl, -C3-6cycloalkyl, -C1alkyl (C3-6cycloalkyl), -C3-6alkenyl and -C3-6alkynyl; 'n' in each case represents an integer, selected from 1, 2 or 3; 'm' in each case represents an integer, selected from 0-3, inclusive. Invention also relates to a compound of formula (Id), where radicals are described in patent claim.;EFFECT: obtaining novel heterocyclic compounds effective as antagonists of cysteinyl-leukotriene.;9 cl, 1 dwg, 2 tbl, 67 ex;
机译:技术领域本发明涉及有机化学,特别是涉及式(IA)的杂环化合物或其药学上可接受的盐,其中在每种情况下,R 1 和R 3 独立地选自氢,卤素,-OH,-C 1-2 烷基,-OC 1-2 烷基,-OC 1 卤代烷氧基,-N(C 1 烷基) 2 ; R 2 代表氢; W代表选自-CH =或-N =的基团; X代表选自-CH = CH-或-N = CH-的基团,其中-N = CH-的氮直接与环“ a”键合; Y代表选自-CH = CH-或-C≡C-的基团; Z表示选自-(CH 2 n -和-CH = CH-的键或基团; A是选自-OR,-O(CH 2 n 苯基,-O(CH 2 n < / Sub>噻吩; P选自-O-; Q是选自-COOH的基团;其中R选自氢,-C 1-6 烷基,-C 3-6 环烷基,-C 1 烷基( C 3-6 环烷基),-C 3-6 烯基和-C 3-6 炔基;在每种情况下,n代表一个整数,选自1、2或3;每种情况下的'm'代表一个整数,从0-3(含0和3)中选择。本发明还涉及式(Id)的化合物,其中基团在专利权利要求中描述。效果:获得有效作为半胱氨酰-白三烯拮抗剂的新型杂环化合物。9 cl,1 dwg,2 tbl,67 ex;

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