Acetic Anhydride → 1-Acetyl-6-fluoro-1,3-dihydro-2H-indol-2-one
Reaction equation
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][C:7](=[O:11])[NH:8]2)=[CH:4][CH:3]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>>[C:12]([N:8]1[C:9]2[C:5](=[CH:4][CH:3]=[C:2]([F:1])[CH:10]=2)[CH2:6][C:7]1=[O:11])(=[O:14])[CH3:13]Participants
3
Procedure
82.5 g 6-fluoro-2-indolinone (educt IV) are stirred in 180 ml acetic anhydride for 3 hours at 130° C. After cooling to ambient temperature the precipitate is suction filtered, washed with 100 ml of petroleum ether and dried.
Workup
- filtrationfiltered
- washwashed with 100 ml of petroleum ether
- customdried
Sources & evidence
- ORD record
- ord-35f07def8a1a43688f4d240ec387559b
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07514468B2
Reaction notes
Loading…