首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis of 3-Chloro-1-(2-chlbro-1,8-naphthyridin-7-yl)-4-arylazetidin-2-ones and 3-(2-Chloro-1,8-naphthyridine-7-yl)-2-arylthiazoIidin-4-ones From 2-Amino-7-chloro-1,8-naphthyridine
【24h】

Synthesis of 3-Chloro-1-(2-chlbro-1,8-naphthyridin-7-yl)-4-arylazetidin-2-ones and 3-(2-Chloro-1,8-naphthyridine-7-yl)-2-arylthiazoIidin-4-ones From 2-Amino-7-chloro-1,8-naphthyridine

机译:3-氯-1-(2-氯-1,8-萘啶-7-基)-4-芳氮杂环丁酮-2-酮和3-(2-氯-1,8-萘啶-7-基)-的合成来自2-氨基-7-氯-1,8-萘啶的2-芳基噻唑烷--4-酮

获取原文
获取原文并翻译 | 示例
       

摘要

2-Amino-7-chloro-1,8-napthyridine(1)undergoes condensation with different aromatic aldehydes to form 2-arylideneamino-7-chloro-1,8-naphthyridines(2-6).These imines when treated with different reagents varied substituted derivatives are produced.Compounds 2-6 are converted to different dyes(7-11)by diazotization.Azetidinones(12-16)are obtained by the reaction of 2-6 and chloroacetylchloride in presence of triethylamine.Finally the imines are converted to thiazolidinones(17-21)by treating compounds with thioglycolic acid.
机译:2-氨基-7-氯-1,8-萘啶(1)与不同的芳族醛缩合形成2-芳基亚氨基-7-氯-1,8-萘啶(2-6),这些亚胺用不同的试剂处理生成各种取代的衍生物,将化合物2-6通过重氮化转化为不同的染料(7-11)。在三乙胺存在下,2-6与氯乙酰氯反应制得氮杂环丁酮(12-16),最后将亚胺转化通过用巯基乙酸处理化合物可生成噻唑烷酮(17-21)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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