4-Fluorobenzoic Acid → HCID 56654151, compound
Reaction equation
Cl.Cl.[NH2:3][CH2:4][C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]2[CH:18]=[C:17]([O:19][CH2:20][CH:21]([CH3:23])[CH3:22])[N:16]=[CH:15][N:14]=2)[CH2:9][CH2:8]1)=[O:6].[F:24][C:25]1[CH:33]=[CH:32][C:28]([C:29](O)=[O:30])=[CH:27][CH:26]=1>>[F:24][C:25]1[CH:33]=[CH:32][C:28]([C:29]([NH:3][CH2:4][C:5]([N:7]2[CH2:12][CH2:11][N:10]([C:13]3[CH:18]=[C:17]([O:19][CH2:20][CH:21]([CH3:23])[CH3:22])[N:16]=[CH:15][N:14]=3)[CH2:9][CH2:8]2)=[O:6])=[O:30])=[CH:27][CH:26]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 3 using 2-amino-1-(4-(6-isobutoxypyrimidin-4-yl)piperazin-1-yl)ethanone dihydrochloride and 4-fluorobenzoic acid.
Sources & evidence
- ORD record
- ord-2d814f7359e144fe8f2dbb03a8e6c929
- Source dataset
- uspto-grants-2015_04
- Patent number
- US08999974B2
Reaction notes
Loading…