Hydrochloric Acid → HCID 11784360, compound
Reaction equation
C[O:2][C:3]([CH2:5][CH:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[N:10]([C:17](=[O:29])[C:18]2[CH:23]=[CH:22][C:21]([NH:24][CH2:25][CH2:26][CH3:27])=[CH:20][C:19]=2[Cl:28])[CH2:9][CH2:8][CH2:7]1)=[O:4].[OH-].[Na+].Cl>C(O)C>[C:3]([CH2:5][CH:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[N:10]([C:17](=[O:29])[C:18]2[CH:23]=[CH:22][C:21]([NH:24][CH2:25][CH2:26][CH3:27])=[CH:20][C:19]=2[Cl:28])[CH2:9][CH2:8][CH2:7]1)([OH:4])=[O:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The above product, 5-methoxycarbonylmethyl-1-(4-n-propylamino-2-chlorobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (880 mg) is dissolved in ethanol (20 ml), and thereto is added a 6N aqueous sodium hydroxide solution (1 ml), and the mixture is stirred overnight at room temperature. The mixture is acidified with hydrochloric acid, and extracted with ethyl acetate. The extract is dried, and concentrated to give 5-carboxymethyl-1-(4-n-propylamino-2-chlorobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (800 mg) as a white powder.
Workup
- extractionextracted with ethyl acetate
- customThe extract is dried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-98369b32a4f84ad586e8b4e332d469a4
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06096736
Reaction notes
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