Sodium Iodide → HCID 17830871, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]([C:12](=[O:22])[C:13]3[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][C:14]=3[O:20][CH3:21])[CH2:10][CH2:9][CH2:8][CH:7]([CH2:23][C:24]([O:26][CH3:27])=[O:25])[C:6]=2[CH:28]=1.C(=O)([O-])[O-].[Na+].[Na+].[Br-].[Br-].[C:37]1([CH3:44])[C:38]([CH3:43])=[CH:39][CH:40]=[CH:41][CH:42]=1.[I-].[Na+]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]([C:12](=[O:22])[C:13]3[CH:18]=[CH:17][C:16]([N:19]4[CH2:43][C:38]5[C:37](=[CH:42][CH:41]=[CH:40][CH:39]=5)[CH2:44]4)=[CH:15][C:14]=3[O:20][CH3:21])[CH2:10][CH2:9][CH2:8][CH:7]([CH2:23][C:24]([O:26][CH3:27])=[O:25])[C:6]=2[CH:28]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 65 °C
Procedure
To a suspension of 7-chloro-5-methoxycarbonylmethyl-1-(2-methoxy-4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (2.6 g) in ethanol (100 ml) are added sodium carbonate (1.5 g), o-xylene dibromide (1.87 g) and sodium iodide (2.42 g), and the mixture is stirred at 60-70° C. for three hours. The mixture is evaporate to remove the solvent, and to the residue is added water, and the mixture is extracted with ethyl acetate. The extract is dried, and evaporate to remove the solvent. The residue is purified by silica gel column chromatography (solvent; ethyl acetate:n-hexane =1:10→1:5) to give 7-chloro-5-methoxycarbonylmethyl-1-[2-methoxy-4-(2-isoindolinyl)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.32 g) as colorless amorphous.
Workup
- customThe mixture is evaporate
- customto remove the solvent
- additionto the residue is added water
- extractionthe mixture is extracted with ethyl acetate
- customThe extract is dried
- customevaporate
- customto remove the solvent
- customThe residue is purified by silica gel column chromatography (solvent; ethyl acetate:n-hexane =1:10→1:5)
Sources & evidence
- ORD record
- ord-d386f26d0c3642958cb32bfc306d9179
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06096735
Reaction notes
Loading…