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Dimethylformamide → 2-(2,6-dichlorophenyl)-3H-benzimidazole-5-carbonyl chloride hydrochloride

HRID 1360734
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인쇄 미리보기

반응식

HRID 1360734 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[NH:10][C:11]2[CH:17]=[C:16]([C:18]([OH:20])=O)[CH:15]=[CH:14][C:12]=2[N:13]=1.CN(C=O)C.C(Cl)[Cl:27]>S(Cl)(Cl)=O>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[NH:10][C:11]2[CH:17]=[C:16]([C:18]([Cl:27])=[O:20])[CH:15]=[CH:14][C:12]=2[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 6344DichloromethaneHCID 433492922-(2,6-Dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid

생성물 1

HCID 866328172-(2,6-dichlorophenyl)-3H-benzimidazole-5-carbonyl chloride hydrochloride

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

실험 절차

A mixture of 2-(2,6-dichlorophenyl)-3H-benzoimidazole-5-carboxylic acid (5 g) in thionyl chloride (10 mL) containing a catalytic quantity of DMF was stirred at RT for 18 h. Methylene chloride was added and the resulting solid was filtered, washed with methylene chloride and dried under reduced pressure to give the title compound as an off-white solid.

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후처리

  1. filtrationthe resulting solid was filtered
  2. washwashed with methylene chloride
  3. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-51180d61d80240ba957d2b1a9bbdfbab
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879850B2

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