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5-Bromo-N-methoxy-N-methylpyridine-3-carboxamide → HCID 86672126, 화합물

HRID 82282
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HRID 82282 반응식
[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[C:10](I)=[CH:9][N:8]([C:12]([CH3:17])([CH3:16])[CH2:13][O:14][CH3:15])[C:6]=2[N:7]=1.[Br:18][C:19]1[CH:20]=[N:21][CH:22]=[C:23]([CH:30]=1)[C:24](N(OC)C)=[O:25]>>[Br:18][C:19]1[CH:30]=[C:23]([C:24]([C:10]2[C:5]3[CH:4]=[N:3][C:2]([Cl:1])=[N:7][C:6]=3[N:8]([C:12]([CH3:17])([CH3:16])[CH2:13][O:14][CH3:15])[CH:9]=2)=[O:25])[CH:22]=[N:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 184722695-Bromo-N-methoxy-N-methylpyridine-3-carboxamideHCID 866721272-Chloro-5-iodo-7-(2-methoxy-1,1-dimethyl-ethyl)-7H-pyrrolo[2,3-d]pyrimidine

생성물 1

HCID 86672126HCID 86672126, 화합물

실험 절차

The title compound was prepared according to the method described for Preparation 64 using 2-Chloro-5-iodo-7-(2-methoxy-1,1-dimethyl-ethyl)-7H-pyrrolo[2,3-d]pyrimidine (Preparation 259) and 5-Bromo-N-methoxy-N-methyl-nicotinamide to afford the title compound as yellow gum in 34% yield, 900 mg.

후처리

  1. customThe title compound was prepared

출처 및 근거

ORD 기록
ord-5c84d76bd7d5413e9deedb1ad3b31d94
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846698B2

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