2,3-Dichlorobenzoic acid → HCID 73672105, 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.[F:12][C:13]([F:32])([F:31])[C:14]1[N:19]=[CH:18][C:17]([CH:20]([N:23]2[CH2:28][CH2:27][C:26]([F:30])([F:29])[CH2:25][CH2:24]2)[CH2:21][NH2:22])=[CH:16][CH: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]([N:23]1[CH2:24][CH2:25][C:26]([F:30])([F:29])[CH2:27][CH2:28]1)[C:17]1[CH:18]=[N:19][C:14]([C:13]([F:12])([F:31])[F:32])=[CH:15][CH:16]=1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 2-(6-(trifluoromethyl)-3-pyridyl)-2-(4,4-difluoro-piperidin-1-yl)-ethylamine.
Sources & evidence
- ORD record
- ord-de616e63c8f74e029be0aa8d9a23a1e6
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415055B2
Reaction notes
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