Hydrochloric Acid → HCID 14349082, compound
Reaction equation
[C:1](O)(=O)[C:2]([OH:4])=[O:3].[CH3:7][O:8][C:9]1[C:26]([O:27][CH3:28])=[CH:25][C:12]2[CH:13]([O:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:14][NH:15][CH2:16][CH2:17][C:11]=2[CH:10]=1.Cl.[Br:30]N1C(=[O:36])CCC1=O>CO>[C:26]([OH:27])(=[O:36])/[CH:9]=[CH:1]\[C:2]([OH:4])=[O:3].[Br:30][C:22]1[CH:23]=[CH:24][C:19]([O:18][CH:13]2[C:12]3[CH:25]=[C:26]([O:27][CH3:28])[C:9]([O:8][CH3:7])=[CH:10][C:11]=3[CH2:17][CH2:16][NH:15][CH2:14]2)=[CH:20][CH:21]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 7,8-dimethoxy-1-phenoxy-2,3,4,5-tetrahydro-3-benzazepine of Example 35 (6.5 g, 22 mmole) in 300 ml methanol was acidified to pH 1 with ethereal hydrogen chloride. After this solution was cooled with an ice bath, N-bromosuccinimide (4.2 g, 24 mmole) was added. The reaction mixture slowly warmed to ambient temperature, was evaporated, stirred with water, basified with saturated sodium carbonate and was extracted with ethyl acetate-ether. The organic extracts were washed with water, saturated sodium chloride and were dried (anhydrous MgSO4), filtered and evaporated to 8 g of an oil. This oil was converted to the maleate salt (8 g, 74%, m.p. 95°-100° C.) by the addition of ethereal maleic acid of which 4 g was recrystallized twice from isopropanol-ether to give 2.4 g (45%) of 1-(4-bromophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine maleate, d 145°-146° C.
Workup
- temperatureAfter this solution was cooled with an ice bath
- customwas evaporated
- extractionwas extracted with ethyl acetate-ether
- washThe organic extracts were washed with water, saturated sodium chloride
- dry with materialwere dried (anhydrous MgSO4)
- filtrationfiltered
- customevaporated to 8 g of an oil
- additionThis oil was converted to the maleate salt (8 g, 74%, m.p. 95°-100° C.) by the addition of ethereal maleic acid of which 4 g
- customwas recrystallized twice from isopropanol-ether
Sources & evidence
- ORD record
- ord-902cef6902a34cc59d84a67e8f1e8f6f
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04935418
Reaction notes
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