4-(4-Oxocyclohexyl)benzonitrile → N-({1-[4-(4-Cyano-phenyl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide
Reaction equation
O=[C:2]1[CH2:7][CH2:6][CH:5]([C:8]2[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][CH:9]=2)[CH2:4][CH2:3]1.[NH:16]1[CH2:19][CH:18]([NH:20][C:21]([CH2:23][NH:24][C:25](=[O:36])[C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:34])[F:33])[CH:27]=2)=[O:22])[CH2:17]1>>[C:12]([C:11]1[CH:14]=[CH:15][C:8]([CH:5]2[CH2:6][CH2:7][CH:2]([N:16]3[CH2:19][CH:18]([NH:20][C:21]([CH2:23][NH:24][C:25](=[O:36])[C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:33])[F:34])[CH:27]=4)=[O:22])[CH2:17]3)[CH2:3][CH2:4]2)=[CH:9][CH:10]=1)#[N:13]Participants
3
Procedure
The title compound was prepared as a white solid by the reductive amination of 4-(4-oxo-cyclohexyl)-benzonitrile and N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide (as prepared in step B of Example 4) using the procedure described in Step C of Example 4.
Sources & evidence
- ORD record
- ord-b37c600bf970440abca075570b0d3dd5
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513229B2
Reaction notes
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