2-Chlorobenzoic Acid → 2-Chloro-N-(2-isopropoxy-2-(2-methylpyrimidin-5-yl)ethyl)benzamide
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH:11]([O:14][CH:15]([C:18]1[CH:19]=[N:20][C:21]([CH3:24])=[N:22][CH:23]=1)[CH2:16][NH2:17])([CH3:13])[CH3:12]>>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:17][CH2:16][CH:15]([O:14][CH:11]([CH3:13])[CH3:12])[C:18]1[CH:19]=[N:20][C:21]([CH3:24])=[N:22][CH:23]=1)=[O:6]Participants
3
Procedure
From 2-chlorobenzoic acid and 2-isopropoxy-2-(2-methylpyrimidin-5-yl)ethanamine. LCMS (MH+): m/z=334.0, tR (minutes, Method E)=0.52
Sources & evidence
- ORD record
- ord-5948d598d4c34e818687e71b8ebfcf72
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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