4-Pyridinecarboxaldehyde → 2-Fluoro-6-[(pyridin-4-ylmethyl)-amino]-benzoic acid
Reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([F:11])[C:3]=1[C:4]([OH:6])=[O:5].[N:12]1[CH:17]=[CH:16][C:15]([CH:18]=O)=[CH:14][CH:13]=1>>[F:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:2]([NH:1][CH2:18][C:15]2[CH:16]=[CH:17][N:12]=[CH:13][CH:14]=2)[C:3]=1[C:4]([OH:6])=[O:5]Participants
3
Procedure
Prepared by a similar procedure as described for preparation 1A, starting from 2-amino-6-fluorobenzoic acid (Aldrich) and pyridine-4-carbaldehyde. 13C-NMR (DMSO-d6) δ 167.7, 162.7, 150.6, 149.5, 148.6, 133.8, 121.9, 107.3, 102.6, 101.9, 45.0.
Workup
- customPrepared by a similar procedure
Sources & evidence
- ORD record
- ord-f9948d00807b4001a19358390c1f14de
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08034811B2
Reaction notes
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