2-Chlorobenzoic Acid → HCID 73672104, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[F:11][C:12]1[N:17]=[CH:16][C:15]([CH:18]([N:21]2[CH2:26][CH2:25][C:24]([F:28])([F:27])[CH2:23][CH2:22]2)[CH2:19][NH2:20])=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH:20][CH2:19][CH:18]([N:21]1[CH2:26][CH2:25][C:24]([F:28])([F:27])[CH2:23][CH2:22]1)[C:15]1[CH:16]=[N:17][C:12]([F:11])=[CH:13][CH:14]=1)=[O:6]Participants
3
Procedure
From 2-chlorobenzoic acid and 2-(6-fluoro-3-pyridyl)-2-(4,4-difluoro-piperidin-1-yl)-ethylamine.
Sources & evidence
- ORD record
- ord-53c107055d4e4ec1aa9752eaf4fc94e1
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415055B2
Reaction notes
Loading…