1-(p-Chlorophenyl)cyclobutanecarboxylic acid → N-[2-(3-Bromo-4-methoxyphenyl)ethyl]-1-(4-chlorophenyl)cyclobutanecarboxamide
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([C:12]([OH:14])=O)[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[Br:15][C:16]1[CH:17]=[C:18]([CH2:24][CH2:25][NH2:26])[CH:19]=[CH:20][C:21]=1[O:22][CH3:23]>>[Br:15][C:16]1[CH:17]=[C:18]([CH2:24][CH2:25][NH:26][C:12]([C:8]2([C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=3)[CH2:9][CH2:10][CH2:11]2)=[O:14])[CH:19]=[CH:20][C:21]=1[O:22][CH3:23]Participants
3
Procedure
Prepared from 1-(4-chlorophenyl)cyclobutanecarboxylic acid and 2-(3-bromo-4-methoxyphenyl)ethanamine following the procedure described in example 85, step 1.
Sources & evidence
- ORD record
- ord-978d27ff3d1f49339006c3f5b9f3721c
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08653100B2
Reaction notes
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