Ammonia → 2-Amino-5-(4-carbamoyl-phenyl)-N-pyridin-4-yl-nicotinamide
Reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:16]=[CH:15][C:11]([C:12](O)=[O:13])=[CH:10][CH:9]=2)=[CH:4][C:3]=1[C:17](=[O:25])[NH:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1.[NH3:26]>>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:16]=[CH:15][C:11]([C:12](=[O:13])[NH2:26])=[CH:10][CH:9]=2)=[CH:4][C:3]=1[C:17]([NH:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)=[O:25]Participants
3
Procedure
Reaction of 4-[6-amino-5-(pyridin-4-ylcarbamoyl)-pyridin-3-yl]-benzoic acid with ammonia gives “A88”; method 1: HPLC/MS: 1.10 min, [M+H]=334;
Workup
- customgives “A88”
- custom1.10 min, [M+H]=334
Sources & evidence
- ORD record
- ord-c09d451b7b944f82a4ac136516c256e0
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09273029B2
Reaction notes
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