Nicotinic Acid → HCID 73425723, compound
Reaction equation
[NH2:1][C:2]1[C:10]([F:11])=[C:9]2[C:5]([C:6]([CH3:15])([CH3:14])[C:7](=[O:13])[N:8]2[CH3:12])=[CH:4][CH:3]=1.[C:16](O)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[N:19][CH:18]=1>>[F:11][C:10]1[C:2]([NH:1][C:16](=[O:23])[C:17]2[CH:22]=[CH:21][CH:20]=[N:19][CH:18]=2)=[CH:3][CH:4]=[C:5]2[C:9]=1[N:8]([CH3:12])[C:7](=[O:13])[C:6]2([CH3:15])[CH3:14]Participants
3
Procedure
Prepared in analogy to example 26 from 6-amino-7-fluoro-1,3,3-trimethylindolin-2-one (example 13d) and nicotinic acid. The title compound was obtained as off-white crystals.
Sources & evidence
- ORD record
- ord-292f93b0e9c649cb88e08164687c15b0
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221816B2
Reaction notes
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