2-Methoxybenzoyl chloride → 1-(2-methoxyphenyl)-1-oxo-2-aza-4-(R)-ethyl-4-phenylbutane
Reaction equation
[C:1]1([C@@H:7]([CH2:10][CH3:11])[CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:12][O:13][C:14]1[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16](Cl)=[O:17]>>[CH3:12][O:13][C:14]1[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16](=[O:17])[CH2:11][CH2:10][C@@H:7]([CH2:8][NH2:9])[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
The title compound was prepared from 0.2 gm of (R)-(−)-2-phenylbutyl amine and 2-mL of 4 methoxybenzoyl chloride according to procedures described in Example 2.
Sources & evidence
- ORD record
- ord-8b06200c802f4a238cfcdbbb2e19237a
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06194458B1
Reaction notes
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