Pyridine → Methyl 4-[6-(cyclopentyloxycarbonyl)amino-3-methoxyindazol-1-ylmethyl]-3-methoxybenzoate

HRID 1080786노트

반응식

HRID 1080786 반응식
Cl[C:2]([O:4][CH:5]1[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:3].[NH2:10][C:11]1[CH:19]=[C:18]2[C:14]([C:15]([O:33][CH3:34])=[N:16][N:17]2[CH2:20][C:21]2[CH:30]=[CH:29][C:24]([C:25]([O:27][CH3:28])=[O:26])=[CH:23][C:22]=2[O:31][CH3:32])=[CH:13][CH:12]=1.N1C=CC=CC=1>ClCCl.C(OCC)(=O)C>[CH3:28][O:27][C:25](=[O:26])[C:24]1[CH:29]=[CH:30][C:21]([CH2:20][N:17]2[C:18]3[C:14](=[CH:13][CH:12]=[C:11]([NH:10][C:2]([O:4][CH:5]4[CH2:9][CH2:8][CH2:7][CH2:6]4)=[O:3])[CH:19]=3)[C:15]([O:33][CH3:34])=[N:16]2)=[C:22]([O:31][CH3:32])[CH:23]=1

참가 물질

6

실험 절차

Cyclopentyl chloroformate (0.17 ml.) was added to a cooled (-20° C.) solution of methyl 4-[6-amino-3-methoxyindazol-1-ylmethyl]-3-methoxybenzoate (S) (0.381 g.) and pyridine (0.11 ml.) in dichloromethane (3.0 ml.). After warming to ambient temperature, the mixture was diluted with ethyl acetate, and washed with hydrochloric acid (1N), water, brine, dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica gel (56 g.), eluting with 5:95 v/v ethyl acetate: dichloromethane, to give the title compound (0.365 g., 75%) as an oil, with satisfactory NMR spectral data.

후처리

  1. washwashed with hydrochloric acid (1N), water, brine
  2. dry with materialdried (MgSO4)
  3. customevaporated
  4. customThe residue was purified by flash chromatography on silica gel (56 g.)
  5. washeluting with 5:95 v/v ethyl acetate

출처 및 근거

ORD 기록
ord-0a6bc8a57fb84de4a5579a8470962f7f
출처 데이터셋
uspto-grants-1996_12
특허 번호
US05583152

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