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

HRID 1080786Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1080786
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

Komponenten

6

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-0a6bc8a57fb84de4a5579a8470962f7f
Quelldatensatz
uspto-grants-1996_12
Patentnummer
US05583152

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