4-Chlorobenzoic Acid → HCID 16730305, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([NH:9][C:10](=[O:18])[C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[N:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[Cl:8].[Cl:19][C:20]1[CH:28]=[CH:27][C:23]([C:24](O)=[O:25])=[CH:22][CH:21]=1>>[Cl:17][C:14]1[CH:15]=[CH:16][C:11]([C:10]([NH:9][C:4]2[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([NH:1][C:24](=[O:25])[C:23]3[CH:27]=[CH:28][C:20]([Cl:19])=[CH:21][CH:22]=3)[CH:3]=2)=[O:18])=[CH:12][N:13]=1Participants
3
Procedure
N-(3-amino-4-chlorophenyl)-6-chloronicotinamide (0.71 mmol) was used in general procedure 2 with 4-chlorobenzoic acid (0.78 mmol). The product was purified by RP-HPLC to give 6-chloro-N-(4-chloro-3-(4-chlorobenzamido)phenyl)nicotinamide. MS (Q1) 419.8 (M)+
Workup
- customThe product was purified by RP-HPLC
Sources & evidence
- ORD record
- ord-9a86bcb59bd74517a823a635a3f898da
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08101610B2
Reaction notes
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