Hydrochloric Acid → HCID 14800369, compound

HRID 258098Notes

Reaction equation

HRID 258098 reaction equation
C([O:4][C:5]1[CH:6]=[C:7]([CH:39]=[CH:40][C:41]=1[O:42]C(=O)C)[CH2:8][N:9]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[C:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[N:12][CH:11]([NH:26][C:27]([C:29]2[NH:30][C:31]3[C:36]([CH:37]=2)=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:28])[C:10]1=[O:38])(=O)C.CO.C(=O)([O-])[O-].[K+].[K+].Cl>O.C(OCC)(=O)C.O1CCCC1>[OH:4][C:5]1[CH:6]=[C:7]([CH:39]=[CH:40][C:41]=1[OH:42])[CH2:8][N:9]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[C:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[N:12][CH:11]([NH:26][C:27]([C:29]2[NH:30][C:31]3[C:36]([CH:37]=2)=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:28])[C:10]1=[O:38]

Participants

8

Procedure

A mixture of (3RS)-1-(3,4-diacetoxybenzyl)-1,3-dihydro-3-(2-indolylcarbonylamino)-5-phenyl-2H-1,4-benzodiazepine-2-one (287 mg), methanol (5 ml), tetrahydrofuran (5 ml), water (1 ml) and 1N aqueous potassium carbonate (5 ml) was stirred for 1.0 hour at 0°-5° C. and then adjusted to pH 1-2 with 6N hydrochloric acid. Ethyl acetate (50 ml) and water (50 ml) were added to the mixture under stirring. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel with an eluent of a mixture of chloroform and ethyl acetate (4:1) to give (3RS)-1-(3,4-dihydroxybenzyl)-3-(2-indolylcarbonylamino)-5-phenyl-2H-1,4-benzodiazepine-2-one (155 mg).

Workup

  1. stirringunder stirring
  2. washThe separated organic layer was washed with water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customThe residue was chromatographed on silica gel with an eluent of a mixture of chloroform and ethyl acetate (4:1)

Sources & evidence

ORD record
ord-d29d3a60827b42b7bf6ae5b3e7673187
Source dataset
uspto-grants-1993_11
Patent number
US05264433

Reaction notes

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