2,3-Dichlorobenzoic acid → HCID 73672828, compound
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.[NH2:12][CH2:13][CH:14]([C:23]1[CH:24]=[N:25][C:26]([N:29]([CH3:31])[CH3:30])=[N:27][CH:28]=1)[N:15]1[CH2:20][CH2:19][C:18]([F:22])([F:21])[CH2:17][CH2:16]1>>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:12][CH2:13][CH:14]([N:15]1[CH2:16][CH2:17][C:18]([F:21])([F:22])[CH2:19][CH2:20]1)[C:23]1[CH:24]=[N:25][C:26]([N:29]([CH3:31])[CH3:30])=[N:27][CH:28]=1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 5-(2-amino-1-(4,4-difluoropiperidin-1-yl)ethyl)-N,N-dimethylpyrimidin-2-amine.
Sources & evidence
- ORD record
- ord-57499f473df243a8905bfe06d08283b7
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415055B2
Reaction notes
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