2,3-Dichlorobenzoic acid → HCID 86716046, 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]=[CH:25][C:26](=[O:30])[N:27]([CH3:29])[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[CH2:20][CH2:19][C:18]([F:22])([F:21])[CH2:17][CH2:16]1)[C:23]1[CH:24]=[CH:25][C:26](=[O:30])[N:27]([CH3:29])[CH:28]=1)=[O:6]Participants
3
Procedure
From 2,3-dichlorobenzoic acid and 5-(2-amino-1-(4,4-difluoropiperidin-1-yl)ethyl)-1-methylpyridin-2(1H)-one.
Sources & evidence
- ORD record
- ord-518a9df5acce48608989f1fd121d546a
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09415055B2
Reaction notes
Loading…