Water → HCID 19607844, compound
Reaction equation
[CH3:1][N:2]([CH3:34])[CH:3]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]([C:14](=[O:33])[C:15]2[CH:20]=[CH:19][C:18]([NH:21][C:22](=[O:30])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[CH3:29])=[C:17]([O:31]C)[CH:16]=2)[CH2:6][CH2:5][CH2:4]1.B(Br)(Br)Br.O.C(=O)([O-])O.[Na+]>ClCCl>[CH3:34][N:2]([CH3:1])[CH:3]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]([C:14](=[O:33])[C:15]2[CH:20]=[CH:19][C:18]([NH:21][C:22](=[O:30])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[CH3:29])=[C:17]([OH:31])[CH:16]=2)[CH2:6][CH2:5][CH2:4]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 5-dimethylamino-1-[3-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.50 g) in dichloromethane (30 ml) is added dropwise to a solution of 1M boron tribromide in dichloromethane (5.46 ml) at -45° C. After completion of the dropping, the mixture is stirred for 1 day while the temperature of the reaction mixture is gradually raised to room temperature. To the reaction solution is added water and the mixture is neutralized with sodium hydrogen carbonate, and extracted with dichloromethane. The extract is washed with saturated saline solution and dried over magnesium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (eluent; chloroform:methanol=500:1), and recrystallized from methanol/diethyl ether to give 5-dimethylamino-1-[3-hydroxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.33 g) as white powder, m.p. 201.5°-202.5° C.
Workup
- extractionextracted with dichloromethane
- washThe extract is washed with saturated saline solution
- dry with materialdried over magnesium sulfate
- distillationThe solvent is distilled off
- customthe resulting residue is purified by silica gel column chromatography (eluent; chloroform:methanol=500:1)
- customrecrystallized from methanol/diethyl ether
Sources & evidence
- ORD record
- ord-cf949874a0554a90860e0a5965f4d399
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05559230
Reaction notes
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