2,3-Dichlorobenzoic acid → 2,3-Dichloro-N-[3-cyclopropyl-2-[2-(trifluoromethyl)pyrimidin-5-yl]propyl]benzamide
Reaction equation
[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[F:12][C:13]([F:28])([F:27])[C:14]1[N:19]=[CH:18][C:17]([CH:20]([CH2:23][CH:24]2[CH2:26][CH2:25]2)[CH2:21][NH2:22])=[CH:16][N:15]=1>>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:22][CH2:21][CH:20]([C:17]1[CH:16]=[N:15][C:14]([C:13]([F:28])([F:27])[F:12])=[N:19][CH:18]=1)[CH2:23][CH:24]1[CH2:26][CH2:25]1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 2-(2-trifluoromethyl-pyrimidin-5-yl)-3-cyclopropyl-propylamine. LCMS (MH+): m/z=418.1, tR (minutes, Method G)=2.55
Sources & evidence
- ORD record
- ord-ccef48bbc136488fbe2d1bf3e11e4ea0
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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