2-Pyridinemethanamine → HCID 67239804, compound
Reaction equation
[OH:1][CH:2]([CH:6]([NH:14][C:15](=[O:33])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][C:17]=1[N:22]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[N:23]1)[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:3]([OH:5])=O.[N:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[CH2:40][NH2:41]>>[OH:1][CH:2]([C:3](=[O:5])[NH:41][CH2:40][C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][N:34]=1)[CH:6]([NH:14][C:15](=[O:33])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][C:17]=1[N:22]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[N:23]1)[CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1Participants
3
Procedure
The reaction was carried out in analogy to reaction step 1.3 by reacting 2-hydroxy-4-phenyl-3-(2-(3-phenyl-1H-pyrazol-1-yl)nicotinamido)butanoic acid with pyridin-2-ylmethylamine; ESI-MS [M+H]+: 533.2
Workup
- customThe reaction was carried out in analogy to reaction step 1.3
Sources & evidence
- ORD record
- ord-82843493df5442d489aaf26ce64c7b03
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598211B2
Reaction notes
Loading…