Diethylamine → 2-Amino-5-(4-diethylcarbamoyl-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]([OH:14])=O)=[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.[CH2:26]([NH:28][CH2:29][CH3:30])[CH3:27]>>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:16]=[CH:15][C:11]([C:12](=[O:14])[N:28]([CH2:29][CH3:30])[CH2:26][CH3:27])=[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 diethyl amine gives “A87”; method 1: HPLC/MS: 1.36 min, [M+H]=390;
Workup
- customgives “A87”
- custom1.36 min, [M+H]=390
Sources & evidence
- ORD record
- ord-3113c6bfc75e418dac8e54f1badf3220
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09273029B2
Reaction notes
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