Methyl Bromide → HCID 10136004, compound
Reaction equation
[CH3:1][Br:2].[C:3]([N:7]([CH3:25])[CH2:8][CH2:9][C@@H:10]([C:17]1[CH:22]=[C:21]([CH3:23])[CH:20]=[CH:19][C:18]=1[OH:24])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([CH3:6])([CH3:5])[CH3:4]>>[Br-:2].[C:3]([N+:7]([CH3:1])([CH3:25])[CH2:8][CH2:9][C@@H:10]([C:17]1[CH:22]=[C:21]([CH3:23])[CH:20]=[CH:19][C:18]=1[OH:24])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([CH3:6])([CH3:5])[CH3:4]Participants
3
Procedure
Following the general procedure of Example 2 and making non critical variations, but starting with methyl bromide and 2-{(1R)-3-[tert-butyl(methyl)amino]-1-phenylpropyl}-4-methylphenol, the title compound is obtained.
Sources & evidence
- ORD record
- ord-45c467a6e88b423b97e27b5f05f3254f
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07439397B2
Reaction notes
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