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2-Amino-6-methylbenzothiazole → N-(6-methylbenzo[d]thiazol-2-yl)-1H-imidazole-1-carboxamide

HRID 920130
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인쇄 미리보기

반응식

HRID 920130 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH2:9])[S:8][C:4]=2[CH:3]=1.[N:12]1([C:17](N2C=CN=C2)=[O:18])[CH:16]=[CH:15][N:14]=[CH:13]1>CN(C=O)C>[CH3:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH:9][C:17]([N:12]3[CH:16]=[CH:15][N:14]=[CH:13]3)=[O:18])[S:8][C:4]=2[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 173352-Amino-6-methylbenzothiazoleHCID 682631,1'-Carbonyldiimidazole

생성물 1

HCID 59427382N-(6-methylbenzo[d]thiazol-2-yl)-1H-imidazole-1-carboxamide수율 99%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
25 °C

실험 절차

To a solution of 6-methylbenzo[d]thiazol-2-amine (109, 328 mg, 2 mmol, Sigma-Aldrich) in DMF (5 mL) was added di(1H-imidazol-1-yl)methanone (110, 357 mg, 2.2 mmol, Sigma-Aldrich) at 0° C. Under vigorous stirring, the resulting reaction mixture was slowly allowed to warm to a temperature of about 25° C. over 14 h. A white precipitate formed. The precipitate was collected by filtration under reduced pressure, washed twice with EtOAc (10 mL for each wash), and dried under reduced pressure to provide 108 (yield >99%).

후처리

  1. customUnder vigorous stirring, the resulting reaction mixture
  2. customA white precipitate formed
  3. filtrationThe precipitate was collected by filtration under reduced pressure
  4. washwashed twice with EtOAc (10 mL for
  5. washeach wash), and
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-908c9f7f497e4013bcf80fd5870fb47a
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273043B2

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