首页> 外国专利> 1-Fluoro:phenyl-1,8-naphthyridine-3-carboxylic acid derivs. prodn. - some being new by reacting formamide acetal with pyridyl-acetate ester, and new intermediates, useful as bactericides

1-Fluoro:phenyl-1,8-naphthyridine-3-carboxylic acid derivs. prodn. - some being new by reacting formamide acetal with pyridyl-acetate ester, and new intermediates, useful as bactericides

机译:1-氟:苯基-1,8-萘啶-3-羧酸衍生物。产品-一些是通过使甲酰胺缩醛与乙酸吡啶酯反应而获得的新化合物,以及用作杀菌剂的新中间体

摘要

Prodn. of naphthyridine derivs. of formula (I) or their salts comprises reacting nicotinoyl-acetic acid cpds. (II) with formamide acetal (II), opt. in the presence of an acoid anhydirde, and if required removal of protecting gps. or conversion to a salt or ester. In the formulae, R1 = H or protecting gp. R2 = halo, OH, N3 or (all opt. substd.) alkoxy, alkylthio, arylthio, alkane- or arene-sulphinyl or -sulphonyl, di(alkoxy or aryloxy) phosphinyloxy, or (both opt. N-protected) 3-aminopyrrolidino or piperazino X = H or F R1a = protecting gp. R3 and R4 = alkyl or cycloalkyl or together are alkylene complating the -CH(O)-O- ring R5 and R6 = alkyl, or together complete a heterocycle. (I) are new cpds. where R2 is other than halo or opt. protected 3-aminopyrrolidino or piperazino. Also new are intermediates (II) and their percursors of formula (IV).
机译:产品萘啶的衍生物。式(I)的化合物或其盐包括使烟酰乙酸cpds反应。 (II)与甲酰胺缩醛(II),同上。在有酸酐的情况下,并在需要时除去保护性gps。或转化为盐或酯。式中,R 1 = H或保护性gp。 R 2 =卤素,OH,N 3或(均优选)烷氧基,烷硫基,芳硫基,烷烃-或芳烃-亚磺酰基或-磺酰基,二(烷氧基或芳氧基)次膦酰基氧基或(均受N-保护的)3-氨基吡咯烷或哌嗪子X = H或F R1a =保护gp。 R 3和R 4 =烷基或环烷基,或一起是构成-CH(O)-O-环的亚烷基,R 5和R 6 =烷基,或一起构成一个完整的杂环。 (I)是新的cpds。其中R2不是卤素或opt。受保护的3-aminopyrrolidino或piperazino。中间体(II)及其式(IV)的前体也是新的。

著录项

  • 公开/公告号ES8702362A1

    专利类型

  • 公开/公告日1986-12-16

    原文格式PDF

  • 申请/专利权人 TOYAMA CHEMICAL CO. LTD.;

    申请/专利号ES19860551134

  • 发明设计人

    申请日1986-01-22

  • 分类号C07D221/14;A61K31/435;

  • 国家 ES

  • 入库时间 2022-08-22 07:17:15

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