Isonicotinic Acid → N-({[Bis-(3-fluoro-phenyl)-methyl]-carbamoyl}-methyl)-isonicotinamide
Reaction equation
[NH2:1][CH2:2][C:3]([NH:5][CH:6]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([F:20])[CH:15]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[CH:8]=1)=[O:4].[C:21](O)(=[O:28])[C:22]1[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=1>>[F:20][C:16]1[CH:15]=[C:14]([CH:6]([NH:5][C:3]([CH2:2][NH:1][C:21](=[O:28])[C:22]2[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=2)=[O:4])[C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[CH:8]=2)[CH:19]=[CH:18][CH:17]=1Participants
3
Procedure
Prepared in analogy to example 1.12 from 2-amino-N-[bis-(3-fluoro-phenyl)-methyl]-acetamide (example 3.4) and isonicotinic acid.
Sources & evidence
- ORD record
- ord-d76acc28f18441d198fc8b2e5f9dd59e
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964645B2
Reaction notes
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