首页> 外国专利> New 6alphaalpha - alkyl (c1-c4) - 3 - (C1 - C4) - alkoxy 2,3,5,6,6alpha, 8 - hexahidro 2,3,5,6,6alpha 8.9, respectively.9alphabeta octahidrociclopenta - F - L benzopiran 7 1H - trees and their Derivatives Esterified and etherified substituted at position 3Appropriate as Intermediates in the total synthesis of steroids, devoid of Therapeutic Action and Procedure for obtaining them

New 6alphaalpha - alkyl (c1-c4) - 3 - (C1 - C4) - alkoxy 2,3,5,6,6alpha, 8 - hexahidro 2,3,5,6,6alpha 8.9, respectively.9alphabeta octahidrociclopenta - F - L benzopiran 7 1H - trees and their Derivatives Esterified and etherified substituted at position 3Appropriate as Intermediates in the total synthesis of steroids, devoid of Therapeutic Action and Procedure for obtaining them

机译:新的6alphaalpha-烷基(c1-c4)-3-(C1-C4)-烷氧基2,3,5,6,6alpha,8-六羟基2,3,5,6,6alpha 8.9.9alphabeta octahidrociclopenta-F- L benzopiran 7 1H-树木及其衍生物在3位被酯化和醚化取代适合作为类固醇全合成中的中间体,没有治疗作用和获得它们的步骤

摘要

1431820 Benzopyran derivatives SCHERING AG 7 June 1973 [8 June 1972 (2)] 27236/73 Heading C2C The invention comprises compounds of general Formula II: in which R 1 and R 3 are each C 1 -C 4 alkyl; n is 1 or 2; -A-B- is wherein in the grouping the 9a-hydrogen is trans to the 6a substituent; X is a free, esterified or etherified hydroxyl group and Y is hydrogen, or X and Y together are an oxygen atom; and W is in which V is halogen, Z is a ketalized carbonyl group or a free, esterified or etherified hydroxymethylene group, R 4 and R 5 are C 1 -C 4 alkyl, and R 6 is alkyl, aryl or aralkyl. They may be prepared by cyclization of a compound of Formula IV: in the presence of an acidic catalyst. Any keto group represented by X and Y together with the adjacent carbon atom in the resulting compound may be reduced to form a free hydroxyl group and/or the double bond in the grouping represented by -A-B- may be hydrogenated and/or any free hydroxyl group represented by X may be esterified or etherified.
机译:1431820苯并吡喃衍生物SCHERING AG 1973年6月7日[1972年6月8日(2)] 27236/73标题C2C本发明包含通式II的化合物:其中R 1和R 3各自为C 1 -C 4烷基;和n为1或2; -A-B-其中,在9a-氢的基团中,反式转化为6a-取代基; X为游离,酯化或醚化的羟基,Y为氢,或X和Y一起为氧原子; W为V,其中V为卤素,Z为缩酮化的羰基或游离的,酯化的或醚化的羟亚甲基,R 4和R 5为C 1 -C 4烷基,R 6为烷基,芳基或芳烷基。它们可以通过在酸性催化剂的存在下环化式IV的化合物来制备。 X和Y代表的任何酮基以及相邻化合物中的相邻碳原子都可以还原形成一个游离羟基和/或-AB-代表的基团中的双键可以被氢化和/或任何游离羟基X表示的基团可以被酯化或醚化。

著录项

  • 公开/公告号AR203537A1

    专利类型

  • 公开/公告日1975-09-22

    原文格式PDF

  • 申请/专利权人 SCHERING AG;

    申请/专利号AR19730248482

  • 发明设计人

    申请日1973-06-08

  • 分类号C07D7/26;

  • 国家 AR

  • 入库时间 2022-08-23 04:47:01

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