Hydrochloric Acid → Delapril Hydrochloride
Reaction equation
C(OCC)(=O)C.C(=O)([O-])O.[Na+].Br.[CH2:13]([O:15][C:16]([C@@H:18]([NH:27][C@H:28]([C:30]([N:32]([CH:37]1[CH2:45][C:44]2[C:39](=[CH:40][CH:41]=[CH:42][CH:43]=2)[CH2:38]1)[CH2:33][C:34]([OH:36])=[O:35])=[O:31])[CH3:29])[CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:17])[CH3:14].[ClH:46]>O>[ClH:46].[CH2:13]([O:15][C:16]([C@@H:18]([NH:27][C@H:28]([C:30]([N:32]([CH:37]1[CH2:38][C:39]2[C:44](=[CH:43][CH:42]=[CH:41][CH:40]=2)[CH2:45]1)[CH2:33][C:34]([OH:36])=[O:35])=[O:31])[CH3:29])[CH2:19][CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:17])[CH3:14]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of 500 ml of ethyl acetate, 33 g of sodium hydrogen carbonate and 500 ml of water is added 16.2 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanyl-N-(indan-2-yl)glycine hydrobromide prepared by the procedure of Example 4. After stirring to complete dissolution, the solution was adjusted to pH 4 with 1 N hydrochloric acid. The ethyl acetate layer is separated, washed with water, dried and, after addition of 20 ml of 7 N ethanolic hydrochloric acid, concentrated under reduced pressure. To the residue and added 250 ml of ethyl ether and 250 ml of petroleum ether, and the resulting precipitate is collected by filtration to give 11 g of N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanyl-N-(indan-2-yl)glycine hydrochloride as colorless crystals.
Workup
- customprepared by the procedure of Example 4
- customThe ethyl acetate layer is separated
- washwashed with water
- customdried
- additionafter addition of 20 ml of 7 N ethanolic hydrochloric acid
- concentrationconcentrated under reduced pressure
- additionTo the residue and added 250 ml of ethyl ether and 250 ml of petroleum ether
- filtrationthe resulting precipitate is collected by filtration
Sources & evidence
- ORD record
- ord-42e50726fe1b4af69e217608b6a21416
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05098892
Reaction notes
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