홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

5-Bromo-N-methoxy-N-methylpyridine-3-carboxamide → HCID 70817189, 화합물

HRID 82284
노트
인쇄 미리보기

반응식

HRID 82284 반응식
I[C:2]1[C:10]2[CH:9]=[N:8][CH:7]=[N:6][C:5]=2[N:4]([C:11]([CH3:16])([CH3:15])[CH2:12][O:13][CH3:14])[CH:3]=1.[Br:17][C:18]1[CH:19]=[N:20][CH:21]=[C:22]([CH:29]=1)[C:23](N(OC)C)=[O:24]>>[Br:17][C:18]1[CH:29]=[C:22]([C:23]([C:2]2[C:10]3[CH:9]=[N:8][CH:7]=[N:6][C:5]=3[N:4]([C:11]([CH3:16])([CH3:15])[CH2:12][O:13][CH3:14])[CH:3]=2)=[O:24])[CH:21]=[N:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 184722695-Bromo-N-methoxy-N-methylpyridine-3-carboxamideHCID 70817500HCID 70817500, 화합물

생성물 1

HCID 70817189HCID 70817189, 화합물

실험 절차

The title compound was prepared according to the method described for Preparation 64 using 5-Iodo-7-(2-methoxy-1,1-dimethyl-ethyl)-7H-pyrrolo[2,3-d]pyrimidine (Preparation 262) and 5-Bromo-N-methoxy-N-methyl-nicotinamide to afford the title compound as light brown gum in 51% yield, 3 g.

후처리

  1. customThe title compound was prepared

출처 및 근거

ORD 기록
ord-c4b8f0115ce745628a8d60b3993ed75f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846698B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트