2-Chlorobenzoic Acid → 2-Chloro-N-((4,4-difluoro-1-(2-(difluoromethyl)pyrimidin-5-yl)cyclohexyl)methyl)benzamide
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[F:11][CH:12]([F:29])[C:13]1[N:18]=[CH:17][C:16]([C:19]2([CH2:27][NH2:28])[CH2:24][CH2:23][C:22]([F:26])([F:25])[CH2:21][CH2:20]2)=[CH:15][N:14]=1>>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:28][CH2:27][C:19]1([C:16]2[CH:15]=[N:14][C:13]([CH:12]([F:29])[F:11])=[N:18][CH:17]=2)[CH2:24][CH2:23][C:22]([F:25])([F:26])[CH2:21][CH2:20]1)=[O:6]Participants
3
Procedure
From 2-chlorobenzoic acid and (1-(2-(difluoro methyl)pyrimidin-5-yl)-4,4-difluorocyclohexyl)methanamine. LCMS (MH+): m/z=416.1, tR (minutes, Method F)=2.83
Sources & evidence
- ORD record
- ord-9afe5ebbb02e4f79a4e381c2746723bd
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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