Citric Acid → 4-(5-Iodoindazole-1-yl)-benzoic acid

HRID 1098900

반응식

HRID 1098900 반응식
[NH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)[NH2:2].C(=O)([O-])[O-].[Cs+].[Cs+].F[C:19]1[CH:26]=[CH:25][C:24]([I:27])=[CH:23][C:20]=1[CH:21]=O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN1CCCC1=O>[I:27][C:24]1[CH:23]=[C:20]2[C:19](=[CH:26][CH:25]=1)[N:1]([C:3]1[CH:4]=[CH:5][C:6]([C:7]([OH:9])=[O:8])=[CH:10][CH:11]=1)[N:2]=[CH:21]2

참가 물질

6

실험 절차

4-Hydrazinobenzoic acid (11.32 g, 60 mmol) and cesiumcarbonate (58.65 g, 180 mmol) are added to 2-fluoro-5-iodobenzaldehyde (15 g, 60 mmol) in 300 mL N-methylpyrrolidon. After 1 h stirring at r.t., the reaction is heated for 4 h at 150° C. The reaction mixture is allowed to cool off and poured on 1 L ice water. The reaction mixture is acidified with citric acid and vigorously stirred at r.t. for 30 min. The precipitate is filtered off and given in ethyl acetate. The slurry is vigorously stirred for 1 h and sucked off. The filter residue (few material) is discarded and the filtrate evaporated. This residue which is contaminated with N-methylpyrrolidine is treated with 300 mL of a mixture of ethyl acetate/hexane (1:3) and stirred overnight. The precipitated crystals are sucked off and dried. 17.11 g (78.32%) of 4-(5-iodoindazole-1-yl)-benzoic acid are obtained.

후처리

  1. temperaturethe reaction is heated for 4 h at 150° C
  2. temperatureto cool off
  3. stirringvigorously stirred at r.t. for 30 min
  4. filtrationThe precipitate is filtered off
  5. stirringThe slurry is vigorously stirred for 1 h
  6. customthe filtrate evaporated
  7. additionis treated with 300 mL of a mixture of ethyl acetate/hexane (1:3)
  8. stirringstirred overnight
  9. customdried

출처 및 근거

ORD 기록
ord-449b478386e94682a8ae5fca621a1c9d
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08143290B2

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