Hydrogen Bromide → HCID 21242944, compound
Reaction equation
[Br:1]C1C=C(OC)C2CCN(C)CCC=2C=1.Cl.C[O:18][C:19]1[C:29]2[CH:28]=[CH:27][N:26]([CH3:30])[CH2:25][CH2:24][C:23]=2[CH:22]=[C:21]([S:31]([CH3:34])(=[O:33])=[O:32])[CH:20]=1.Br>>[BrH:1].[OH:18][C:19]1[C:29]2[CH:28]=[CH:27][N:26]([CH3:30])[CH2:25][CH2:24][C:23]=2[CH:22]=[C:21]([S:31]([CH3:34])(=[O:33])=[O:32])[CH:20]=1Participants
4
Procedure
By the same procedure, 8-bromo-6-methoxy-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine is converted to 6-methoxy-3-methyl-8-methylsulfonyl-1H-3-benzazepine hydrochloride which is treated with 48% hydrobromic acid to give 6-hydroxy-3-methyl-8-methylsulfonyl-1H-3-benzazepine hydrobromide.
Sources & evidence
- ORD record
- ord-a69cd478cca3436f81c89e08eab2f3a0
- Source dataset
- uspto-grants-1989_04
- Patent number
- US04824839
Reaction notes
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