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Means for foerderung of the growth or to improve the effectiveness of the feed conversion in animals

机译:促进动物生长或提高饲料转化效率的手段

摘要

1495305 5,7-Dihydroxy-3-phenyl-4-oxo-4H- benzopyran carboxaldehydes PFIZER Ltd 10 Sept 1976 [12 Sept 1975] 37552/75 Heading C2C [Also in Division A5] Novel compounds of the Formula II wherein R is formyl in the 6- or 8-position and RSP1/SP is an optional halogen in the 8- or 6-position respectively ; RSP3/SP is hydrogen or alkyl; RSP4/SP is halogen, hydroxy, C 2-8 -alkanoyloxy, alkyl, alkoxy, nitro, amino, C 2-8 alkanoylamino, sulphonylamino or (SO 2 NRSP5/SPRSP6/SP wherein RSP5/SP and RSP6/SP are hydrogen or alkyl or RSP5/SP and RSP6/SP together with the nitrogen atom form a saturated heterocyclic group and n is 0 to 3, or any two of the moieties RSP4/SP represent alkylenedioxy attached to adjacent carbon atoms of the benzene ring, wherein alkyl alkoxy and alkylene groups have 1 to 4 carbon atoms, may be prepared by (1) where R 1 is hydrogen and (RSP4/SP) n does not contain a free amino or a sulphamoyl group, by heating a compound V with hexamine in glacial acetic acid or by reacting V with hydrogen cyanide, a cyanogen halide or zinc cyanide in the presence of hydrogen chloride or a Lewis acid; (2) where R 1 and R 2 are hydrogen and (RSP4/SP) n is other than or does not contain hydroxy, acyloxy, amino or sulphamoyl, reacting a compound III wherein (RSP9/SP) n is as defined for (RSP4/SP) n immediately above, with at least two molar proportions of dimethyl formamide in the presence of a p-toluene sulphonyl chloride; (3) where R 1 is halogen, by halogenation of compounds II in which R 1 is hydrogen; (iv) where (RSP4/SP) n is or includes amino, by the reduction of the corresponding nitro substituted compound II; (v) optional acylation of the product of (iv) to form an alkanoylamino or sulphonylamino group; (vi) where (RSP4/SP) n is or includes sulphamoyl, by chlorosulphonation followed by reaction with ammonia or a dialkyl or cyclic amine. 5 - Hydroxy - 3 - (4 - methoxyphenyl) - 7 - noctanoyloxy - 4 - oxo - 4H - benzopyran - 8 - carboxaldehydedihydrate, pharmaceutical compositions of which are claimed, is prepared by esterification of the corresponding 5,7-dihydroxy compound.
机译:1495305 5,7-二羟基-3-苯基-4-氧代-4H-苯并吡喃甲醛甲醛PFIZER Ltd 1976年9月10日[1975年9月12日] 37552/75标题C2C [A5也在A5部分]其中R为甲酰基的式II新化合物在6位或8位的卤素原子和R 1 分别是在8位或6位的卤素原子; R 3 是氢或烷基; R 4 是卤素,羟基,C 2-8-烷酰氧基,烷基,烷氧基,硝基,氨基,C 2-8烷酰氨基,磺酰氨基或(SO 2 NR 5 R 6 其中R 5 和R 6 是氢或烷基或R 5 和R 6 与氮原子一起形成饱和杂环基团,并且n为0至3,或部分R 4 中的任何两个代表连接于苯环的相邻碳原子的亚烷基二氧基,其中烷基烷氧基和亚烷基具有1-4个碳原子,可以通过加热化合物V通过以下方法制备:(1)其中R 1是氢并且(R 4 )n不包含游离氨基或氨磺酰基。与六胺在冰醋酸中或在氯化氢或路易斯酸存在下使V与氰化氢,卤化氰或氰化锌反应;(2)其中R 1和R 2为氢和(R SP 4 < / SP>)n与或不包含羟基,酰氧基,氨基或氨磺酰基,与化合物III反应,其中(R 9 )n如上对(R 4 )n的定义,在对甲苯磺酰氯存在下,具有至少两个摩尔比例的二甲基甲酰胺; (3)其中R 1为卤素,通过将其中R 1为氢的化合物II卤化; (iv)其中(R 4 )n为或包括氨基,是通过还原相应的硝基取代的化合物II来实现的; (v)(iv)的产物的任选酰化以形成烷酰基氨基或磺酰基氨基; (vi)其中(R 4 )n为或包括氨磺酰基,通过氯磺化,然后与氨或二烷基或环胺反应。通过相应的5,7-二羟基化合物的酯化制备5-羟基-3-(4-甲氧基苯基)-7-十一烷酰氧基-4-氧代-4H-苯并吡喃-8-羧甲醛二水合物,其药物组合物被要求保护。

著录项

  • 公开/公告号DE2640618A1

    专利类型

  • 公开/公告日1977-03-17

    原文格式PDF

  • 申请/专利权人 PFIZER;

    申请/专利号DE19762640618

  • 申请日1976-09-09

  • 分类号C07D311/36;A23K1/16;A61K31/35;

  • 国家 DE

  • 入库时间 2022-08-22 23:59:29

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