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2,4(OR 2,5)DISUBSTITUTED-4(OR 5)OXAZOLE CARBOXAMIDES

机译:2,4(或2,5)取代的4(或5)恶唑羧酰胺

摘要

1374345 Oxazole derivatives GRUPPO LEPETIT SpA 14 Dec 1972 [7 Aug 1972] 53966/72 Heading C2C Novel oxazole derivatives of the formula wherein A is cyclohexyl, thienyl or phenyl optionally substituted by one or more halogen atoms, or C 1-6 alkyl, halo-C 1-6 alkyl, C 1-6 alkoxy, NO 2 , CN, NH 2 , carbamoyl, sulphamoyl or carboxy radicals, and one of the radicals R 1 and R 2 is C 1-6 alkyl and the other is CON(R 3 )R 4 , wherein R 3 is H, C 1-6 alkyl, C 2-6 alkenyl, cycloalkyl, aryl, aryl-C 1-6 alkyl, hydroxy-C 1-6 alkyl, acyloxy-C 1-6 alkyl, OH, NH 2 , C 1-6 alkylideneamino, cycloalkylideneamino, or aralkylideneamino, and R 2 is H, C 1-6 alkyl, C 2-6 alkenyl, cycloalkyl, aryl, aryl-C 1-6 alkyl, hydroxy- C 1-6 alkyl or acyloxy-C 1-6 alkyl, or R 3 and R 4 , together with the N atom to which they are attached form a 5 to 7 membered saturated heterocyclic ring optionally containing further N, O or S atoms, are prepared by reacting the appropriate C 1-6 alkyl 4-(or 5-)-oxazolecarboxylates or 4- (or 5-)-oxazolecarboxylic acid halides with amines of the formula Alternatively compound in which R 3 is C 1-6 alkylideneamino, cycloalkylideneamino or aralkylideneamino may be obtained by reacting compound in which R 3 is NH 2 with the corresponding aldehydes or ketones, and those in which R 3 and/or R 4 is acyloxy-C 1-6 alkyl by acylating the corresponding hydroxy compounds. Ethyl 2 - phenyl - 4 - methyl - 5 - oxasolecarboxylate, 5 - methyl - 2 - phenyl - 4 - oxazolecarboxylic acid chloride, ethyl 5 - methyl - 2 - (2- thienyl) - 4 - oxazolecarboxylate, ethyl 5 - methyl- 2 - (4 - fluorophenyl) 4 - oxazolecarboxylate, 2- (4 - hclorophenyl) - 5 - methyl - 4- oxazolecarboxylic acid chloride, 5 - methyl - 2 - (p - tolyl) - 4- oxazolecarboxylic acid chloride, and 2-cyclohexyl 5 - methyl - 4 - oxazolecarboxylic acid chloride are obtained by known methods. Pharmaceutical compositions, having antiinflammatory and analgesic activities, contain the above novel compounds together with pharmaceutically acceptable carriers.
机译:1374345恶唑衍生物GRUPPO LEPETIT SpA 1972年12月14日[1972年8月7日]标题C2C具有下式的新型恶唑衍生物,其中A为任选被一个或多个卤素原子取代的环己基,噻吩基或苯基,或C 1-6烷基,卤素-C 1-6烷基,C 1-6烷氧基,NO 2,CN,NH 2,氨基甲酰基,氨磺酰基或羧基,且基团R 1和R 2之一为C 1-6烷基,另一个为CON( R 3)R 4,其中R 3为H,C 1-6烷基,C 2-6烯基,环烷基,芳基,芳基-C 1-6烷基,羟基-C 1-6烷基,酰氧基-C 1-6烷基,OH,NH 2,C 1-6亚烷基亚氨基,环亚烷基亚氨基或芳亚烷基亚氨基,并且R 2是H,C 1-6烷基,C 2-6烯基,环烷基,芳基,芳基-C 1-6烷基,羟基- C 1-6烷基或酰氧基-C 1-6烷基,或R 3和R 4与它们所连接的N原子一起形成5至7元饱和杂环,可选地还包含N,O或S原子,通过使合适的C 1-6烷基4-(或5-)-氧反应制备唑羧酸盐或4-(或5-)-恶唑羧酸卤化物与下式的胺:另外,R 3为C 1-6的亚烷基氨基,环亚烷基氨基或芳烷基亚氨基的化合物可通过使其中R 3为NH 2的化合物与相应的化合物反应而获得。醛或酮,以及其中R 3和/或R 4是酰氧基-C 1-6烷基的那些,可通过酰化相应的羟基化合物来实现。乙基2-苯基-4-甲基-5-恶唑羧酸酯,5-甲基-2-苯基-4-恶唑羧酸氯,乙基5-甲基-2-(2-噻吩基)-4-恶唑羧酸酯,乙基5-甲基-2 -(4-氟苯基)4-恶唑羧酸酯,2-(4-氯苯基)-5-甲基-4-恶唑羧酸氯,5-甲基-2-(对甲苯基)-4-恶唑羧酸氯和2-环己基通过已知方法获得5-甲基-4-恶唑羧酸氯。具有抗炎和止痛活性的药物组合物含有上述新型化合物以及药学上可接受的载体。

著录项

  • 公开/公告号IL40904A

    专利类型

  • 公开/公告日1975-12-31

    原文格式PDF

  • 申请/专利权人 GRUPPO LEPETIT SPA;

    申请/专利号IL19720040904

  • 发明设计人

    申请日1972-11-22

  • 分类号C07D85/44;C07D99/02;

  • 国家 IL

  • 入库时间 2022-08-23 02:53:20

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