3-Chloro-p-anisic acid → (R)-3-chloro-4-methoxy-N-(1-phenylethyl)benzamide
Reaction equation
[C:1]1([C@H:7]([NH2:9])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:10][C:11]1[CH:12]=[C:13]([CH:17]=[CH:18][C:19]=1[O:20][CH3:21])[C:14](O)=[O:15]>>[Cl:10][C:11]1[CH:12]=[C:13]([CH:17]=[CH:18][C:19]=1[O:20][CH3:21])[C:14]([NH:9][C@@H:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH3:8])=[O:15]Participants
3
Procedure
Prepare in a similar manner to example 4 using (R)-1-phenylethanamine and 3-chloro-4-methoxy benzoic acid. MS (M+H, 290.0).
Sources & evidence
- ORD record
- ord-dc4233b861a740af8bab01207c2f2eea
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07476399B2
Reaction notes
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