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1,1'-Carbonyldiimidazole → n-(6-Bromo-1,3-benzothiazol-2-yl)-1h-imidazole-1-carboxamide

HRID 555986
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인쇄 미리보기

반응식

HRID 555986 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH2:9])[S:8][C:4]=2[CH:3]=1.[CH:12]1[N:16]=[CH:15][N:14]([C:17](N2C=NC=C2)=[O:18])[CH:13]=1>C(Cl)Cl>[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH:9][C:17]([N:14]3[CH:13]=[CH:12][N:16]=[CH:15]3)=[O:18])[S:8][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 682631,1'-CarbonyldiimidazoleHCID 851492-Benzothiazolamine, 6-bromo-

생성물 1

HCID 86643867n-(6-Bromo-1,3-benzothiazol-2-yl)-1h-imidazole-1-carboxamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A suspension of 6-bromo-benzothiazol-2-ylamine (5 g, 21.83 mmol) in DCM (250 ml) is treated with CDI (3.54 g, 21.83 mmol) and the reaction mixture is heated to reflux for 2 hours. The reaction mixture is filtered and the resulting solid is dried in the vacuum oven overnight to afford the title compound.

후처리

  1. temperaturethe reaction mixture is heated
  2. temperatureto reflux for 2 hours
  3. filtrationThe reaction mixture is filtered
  4. customthe resulting solid is dried in the vacuum oven overnight

출처 및 근거

ORD 기록
ord-f27298b6cd944f8994516c973546a063
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053574B2

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