where Y means 3-quinolinyl group or 2-indolyl group of the formula (II) where R means hydrogen, acetyl group or group CH2COOR being R means hydrogen or C1-C4-alkyl; X means (hetero)aryl radical taken from a group given in description; Z means hydrogen, C1-C4-alkyl or benzyl, and their salts and solvates also. Invention relates to also a method of synthesis of compounds of the formula (I), intermediate compounds for synthesis and a pharmaceutical composition based on compounds said. Synthesized compounds show agonism with respect to cholecystokinin receptors and can be used for treatment of patients with disorders caused by cholecystokinin. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 12 cl, 4 tbl, 34 ex"/> DERIVATIVES OF POLYSUBSTITUTED 2-AMIDO-4-PHENYLTHIAZOLES, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS FOR SYNTHESIS AND A PHARMACEUTICAL COMPOSITION BASED ON THEREOF
首页> 外国专利> DERIVATIVES OF POLYSUBSTITUTED 2-AMIDO-4-PHENYLTHIAZOLES, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS FOR SYNTHESIS AND A PHARMACEUTICAL COMPOSITION BASED ON THEREOF

DERIVATIVES OF POLYSUBSTITUTED 2-AMIDO-4-PHENYLTHIAZOLES, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS FOR SYNTHESIS AND A PHARMACEUTICAL COMPOSITION BASED ON THEREOF

机译:取代的2-氨基-4-苯基噻唑的衍生物,其合成方法,用于合成的中间化合物和基于其的药物组合物

摘要

FIELD: chemistry of heterocyclic compounds. SUBSTANCE: invention relates to compounds of the formula (I) where Y means 3-quinolinyl group or 2-indolyl group of the formula (II) where R means hydrogen, acetyl group or group CH2COOR being R means hydrogen or C1-C4-alkyl; X means (hetero)aryl radical taken from a group given in description; Z means hydrogen, C1-C4-alkyl or benzyl, and their salts and solvates also. Invention relates to also a method of synthesis of compounds of the formula (I), intermediate compounds for synthesis and a pharmaceutical composition based on compounds said. Synthesized compounds show agonism with respect to cholecystokinin receptors and can be used for treatment of patients with disorders caused by cholecystokinin. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 12 cl, 4 tbl, 34 ex
机译:领域:杂环化合物的化学。物质:本发明涉及式(I)的化合物,其中Y表示3-喹啉基或式(II)的2-吲哚基其中R表示氢,乙酰基或基团CH 2 COOR为R表示氢或C 1 -C 4 -烷基; X表示选自描述中给出的基团的(杂)芳基; Z是指氢,C 1 -C 4 -烷基或苄基,以及它们的盐和溶剂化物。本发明还涉及式(I)的化合物的合成方法,用于合成的中间体化合物以及基于所述化合物的药物组合物。合成的化合物对胆囊收缩素受体表现出激动作用,可用于治疗由胆囊收缩素引起的疾病的患者。效果:改进了合成方法,增强了化合物的有效性。 12厘升,4汤匙,34厘

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