2,6-Dichlorobenzoic acid → 2,6-dichloro-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]=[C:7]([Cl:11])[C:3]=1[C:4]([OH:6])=O.[F:12][CH:13]([F:30])[C:14]1[N:19]=[CH:18][C:17]([C:20]2([CH2:28][NH2:29])[CH2:25][CH2:24][C:23]([F:27])([F:26])[CH2:22][CH2:21]2)=[CH:16][N:15]=1>>[Cl:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:2]([Cl:1])[C:3]=1[C:4]([NH:29][CH2:28][C:20]1([C:17]2[CH:16]=[N:15][C:14]([CH:13]([F:30])[F:12])=[N:19][CH:18]=2)[CH2:25][CH2:24][C:23]([F:26])([F:27])[CH2:22][CH2:21]1)=[O:6]Participants
3
Procedure
From 2,6-dichlorobenzoic acid and (1-(2-(difluoromethyl)pyrimidin-5-yl)-4,4-difluorocyclohexyl)methanamine. LCMS (MH+): m/z=450.1, tR (minutes, Method F)=2.93
Sources & evidence
- ORD record
- ord-fcf96c96a1534c32a5befa128835ca02
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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