首页> 外国专利> METHOD FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE SYNTHESIS OF 1,2,4-TRIAZOLO4,3-APYRIDINES

METHOD FOR THE PREPARATION OF INTERMEDIATES USEFUL FOR THE SYNTHESIS OF 1,2,4-TRIAZOLO4,3-APYRIDINES

机译:合成[1,2,4]-三唑并[4,3-A]嘧啶有用的中间体的制备方法

摘要

The present application discloses a method comprising: (A)(i) admixing a methylnicotinate of Formula (I):wherein R3 is Cl, Br, or I, and R4 is alkyl;with 1,3,5-triazine, and a base, under conditions sufficient to form a naphthyridinone of Formula (II):(ii) admixing the naphthyridinone of Formula (II) with methoxyethanol, a base, and a copper (I) catalyst, under conditions sufficient to form 3-(2-methoxyethoxy)-1,6-naphthyridin-5(6H)-one ("NAPH"):or (B):(i) admixing protected 2-alkoxypyridin-4-ylamine with a lithium reagent, under conditions sufficient to form the protected N-(3-formyl-4-amino-2-alkoxy)pyridine:wherein PG is a protecting groupwherein Rsup8/supis an alkyl group;(ii) admixing the protected N-(3-formyl-4-amino-2-alkoxy)pyridine with 1-hydroxy-2-(2-methoxyethoxy)ethane-1 -sulfonate:and base, under conditions sufficient to form a naphthyridine of Formula (III):; and(iii) acidifying the naphthyridine of Formula (III), under conditions sufficient to form 3-(2-methoxyethoxy)-1,6-naphthyridin-5(6H)-one ("NAPH"):
机译:本申请公开了一种方法,该方法包括:(A)(i)将式(I)的烟酸甲酯与其中的1,3,5-三嗪和碱混合,其中R3为Cl,Br或I,R4为烷基。在足以形成式(II)的萘啶酮的条件下:(ii)在足以形成3-(2-甲氧基乙氧基)的条件下将式(II)的萘啶酮与甲氧基乙醇,碱和铜(I)催化剂混合)-1,6-萘啶-5(6H)-一(“ NAPH”):或(B):(i)在足以形成被保护的N的条件下,将受保护的2-烷氧基吡啶-4-基胺与锂试剂混合-(3-甲酰基-4-氨基-2-烷氧基)吡啶:其中PG为保护基,其中R 8 为烷基;(ii)混合受保护的N-(3-甲酰基-4 -氨基-2-烷氧基)吡啶与1-羟基-2-(2-甲氧基乙氧基)乙烷-1-磺酸盐:和碱,在足以形成式(III)的萘啶的条件下: (iii)在足以形成3-(2-甲氧基乙氧基)-1,6-萘啶-5(6H)-一(“ NAPH”)的条件下酸化式(III)的萘啶:

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