1h-Indazole-1-carboxylic acid,3-(3-fluorophenyl)-5-nitro-,1,1-dimethylethyl ester → 1h-Indazole-1-carboxylic acid,5-amino-3-(3-fluorophenyl)-,1,1-dimethylethyl ester

HRID 503127노트

반응식

HRID 503127 반응식
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([N+:17]([O-])=O)[CH:15]=3)[N:10]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[N:9]=2)[CH:5]=[CH:6][CH:7]=1.[H][H]>O1CCCC1.[Pd]>[C:23]([O:22][C:20]([N:10]1[C:11]2[C:16](=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=2)[C:8]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=2)=[N:9]1)=[O:21])([CH3:26])([CH3:24])[CH3:25]

참가 물질

5

실험 절차

To a solution of 180 mg of tert-butyl 3-(3-fluorophenyl)-5-nitro-1H-1-indazolecarboxylate in 10 ml tetrahydrofuran was added 100 mg of palladium (5%)-carbon, and the mixture was stirred at room temperature in an atmosphere of hydrogen gas at normal pressure for 3 hours. The reaction mixture was filtrated through Celite and the solvent was evaporated, to give 184 mg of the title compound as a light brown oil.

후처리

  1. filtrationThe reaction mixture was filtrated through Celite
  2. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-efc549f82c514b4c9a0a7dbb6497ba3f
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07776890B2

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