首页> 外文期刊>Collection of Czechoslovak Chemical Communications >SOME ASPECTS OF REACTION OF 6-AMINOURACIL AND 6-AMINO-2-THIOURACIL WITH ct,p-UNSATURATED KETONES
【24h】

SOME ASPECTS OF REACTION OF 6-AMINOURACIL AND 6-AMINO-2-THIOURACIL WITH ct,p-UNSATURATED KETONES

机译:6-氨基脲和6-氨基-2-硫代尿嘧啶与ct,p-不饱和酮反应的某些方面

获取原文
获取原文并翻译 | 示例
           

摘要

A number of 5,7-diaryl-5,8-dihydropyrido[2,3-d]pyrimidines and 5,7-diarylpyrido[2,3-d]-pyrimidines were obtained by the reaction of 6-aminouracil derivatives with alpha,beta-unsaturated ketones.Basic catalysts decrease yields of the dihydro derivatives whereas acids increase it.In the reactions of ketones containing the dimethylamino group,elimination of the aryl substituent from position 5 of the pyridopyrimidine system was observed.Some aspects of oxidation of 5,8-dihydropyrido[2,3-d]pyrimidines and synthesis of pyrido[2;3-d]pyrimidines were also investigated.
机译:通过6-氨基尿嘧啶衍生物与α的反应,获得了许多5,7-二芳基-5,8-二氢吡啶并[2,3-d]嘧啶和5,7-二芳基吡啶[2,3-d]-嘧啶。 β-不饱和酮。基本催化剂降低了二氢衍生物的收率,而酸则提高了它。在含有二甲氨基的酮反应中,观察到从嘧啶嘧啶体系第5位的芳基取代基被消除.5氧化的某些方面还研究了8-二氢吡啶并[2,3-d]嘧啶和吡啶并[2; 3-d]嘧啶的合成。

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