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N-[(2-fluoro-5-nitrophenyl)carbamothioyl]benzamide → 5-Nitro-1,3-benzothiazol-2-amine

HRID 723950
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HRID 723950 반응식
C[O-].[Na+].C([NH:12][C:13]([NH:15][C:16]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:17]=1F)=[S:14])(=O)C1C=CC=CC=1>CO>[N+:22]([C:20]1[CH:19]=[CH:18][C:17]2[S:14][C:13]([NH2:12])=[N:15][C:16]=2[CH:21]=1)([O-:24])=[O:23]
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참가 물질

4

반응물 2

HCID 817311N-[(2-fluoro-5-nitrophenyl)carbamothioyl]benzamideHCID 10942334Sodium Methoxide

생성물 1

HCID 27547595-Nitro-1,3-benzothiazol-2-amine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methanol (1.6 L) was added sodium methoxide (8.64 g). While stirring, 1-benzoyl-3-(2-fluoro-5-nitro-phenyl)-thiourea (16 g) was added as a solid and the mixture stirred at room temperature for 17 hours. After this time, the reaction mixture was cooled in an ice bath and then filtered. The precipitate was washed with water (7.10 g, 86%). 1H-NMR δ: 8.05 (d, 1H, J=2.2 Hz), 7.97 (brs, 2H), 7.93 (s, 1H), 7.90 (d, 1H, J=2.2 Hz); MS (ESI) 195.8 (M+1, 100%).

후처리

  1. stirringthe mixture stirred at room temperature for 17 hours
  2. temperatureAfter this time, the reaction mixture was cooled in an ice bath
  3. filtrationfiltered
  4. washThe precipitate was washed with water (7.10 g, 86%)

출처 및 근거

ORD 기록
ord-2bb3380b827d4311a12cc1309e178602
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07141595B2

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