2,3-Dichlorobenzoic acid → 2,3-Dichloro-N-(2-isopropoxy-2-(2-methylpyrimidin-5-yl)ethyl)benzamide

HRID 512377Notes

Reaction equation

HRID 512377 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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