2,3-Dichlorobenzoic acid → 2,3-Dichloro-N-(2-isopropoxy-2-(2-methylpyrimidin-5-yl)ethyl)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.[CH:12]([O:15][CH:16]([C:19]1[CH:20]=[N:21][C:22]([CH3:25])=[N:23][CH:24]=1)[CH2:17][NH2:18])([CH3:14])[CH3:13]>>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:18][CH2:17][CH:16]([O:15][CH:12]([CH3:14])[CH3:13])[C:19]1[CH:20]=[N:21][C:22]([CH3:25])=[N:23][CH:24]=1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 2-isopropoxy-2-(2-methylpyrimidin-5-yl)ethanamine. LCMS (MH+): m/z=368.1, tR (minutes, Method D)=0.64
Sources & evidence
- ORD record
- ord-c186680114804e34a19f22e9689b548c
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102591B2
Reaction notes
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