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Dimethylformamide → 2-(4-bromo-1H-imidazol-1-yl)-3-chloropyridine

HRID 2427118
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인쇄 미리보기

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HRID 2427118 반응식
[Br:1][C:2]1[N:3]=[CH:4][NH:5][CH:6]=1.[Cl:7][C:8]1[C:9](S(C)(=O)=O)=[N:10][CH:11]=[CH:12][CH:13]=1.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C)C=O>O>[Br:1][C:2]1[N:3]=[CH:4][N:5]([C:9]2[C:8]([Cl:7])=[CH:13][CH:12]=[CH:11][N:10]=2)[CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 10796Cesium carbonateHCID 134334253-Chloro-2-methanesulfonylpyridineHCID 178418934HCID 178418934, 화합물

생성물 1

HCID 668538872-(4-bromo-1H-imidazol-1-yl)-3-chloropyridine수율 96.9%

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

A mixture of 1.0 g of 4-bromoimidazole, 1.3 g of 3-chloro-2-(methanesulfonyl)pyridine, 2.7 g of cesium carbonate and 10 ml of N,N-dimethylformamide was stirred at 100° C. for 6 hours. The reaction mixture was allowed to cool to room temperature, and water was poured into the mixture. A deposited precipitate was collected by filtration to obtain 1.7 g of 2-(4-bromo-1H-imidazol-1-yl)-3-chloropyridine of the formula:

후처리

  1. temperatureto cool to room temperature
  2. filtrationA deposited precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-33faa84a5e804a6db083818f7eece76d
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968573B2

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