首页> 外国专利> A SULPHONYL TETRAZOLE COMPOUND, ITS PREPARATION METHOD AND ITS USE FOR PREPARING LAETISPICINE

A SULPHONYL TETRAZOLE COMPOUND, ITS PREPARATION METHOD AND ITS USE FOR PREPARING LAETISPICINE

机译:磺酰四唑化合物,其制备方法及其在制备莱西他滨中的用途

摘要

A sulphonyl tetrazole compound 7 with the following structure, its preparation method and its use for preparing laetispicine. The said sulphonyl tetrazole compound 7, (1-phenyl-5-(3,4-methylenedioxyphenyl ethyl) sulphonyl tetrazole), is obtained from piperonal as raw material and by steps of Darzens condensation, hydrolysis, decarboxylation, reduction, condensation and oxidation. Laetispicine is prepared from the said compound as raw material, by condensation with 9-carbonyl-2E-4E-nonadienoic acid isobutyramide (compound 14), or by reaction with 5-(tetrahydropyran-2-oxo) n-pentanal (compound 10), deprotection, Swern oxidation, Wittig-Horner reaction, hydrolysis and amidation. As shown in H NMR, C NMR, MS and IR, the laetispicine prepared from the above-said compound is consistent with the laetispicine extracted from natural products.
机译:具有以下结构的磺酰基四唑化合物7,其制备方法及其在制备甲氨苄青霉素中的用途。所述磺酰基四唑化合物7(1-苯基-5-(3,4-亚甲基二氧基苯基乙基)磺酰基四唑)是从胡椒醛为原料并通过Darzens缩合,水解,脱羧,还原,缩合和氧化的步骤而获得的。以上述化合物为原料,通过与9-羰基-2E-4E-壬二烯酸异丁酰胺(化合物14)缩合,或与5-(四氢吡喃-2-氧代)正戊醛(化合物10)反应,制备来提西汀,脱保护,Swern氧化,Wittig-Horner反应,水解和酰胺化。如1 H NMR,13 C NMR,MS和IR所示,由上述化合物制备的拉提西汀与从天然产物中提取的拉提西汀一致。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号