3,5-Dichloro-3-(2-methoxyphenyl)indolin-2-one → HCID 67428719, compound
Reaction equation
Cl[C:2]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[O:19][CH3:20])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[NH:4][C:3]1=[O:12].FC(F)(F)C(O)=O.[NH2:28][C:29]([CH3:36])([CH3:35])[C:30]([N:32]([CH3:34])[CH3:33])=[O:31]>>[Cl:11][C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[NH:4][C:3](=[O:12])[C:2]2([NH:28][C:29]([CH3:36])([CH3:35])[C:30]([N:32]([CH3:34])[CH3:33])=[O:31])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[O:19][CH3:20]Participants
3
Procedure
With 868 mg of 3,5-dichloro-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one and the compound obtained in Step 255-3 (3.10 mmol, crude form) as starting materials, 1.02 g of the title compound (colorless amorphous) was obtained by a similar method to Step 4-2.
Sources & evidence
- ORD record
- ord-a6ab4d720d5841fcbe417286bbb15e6e
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030499B2
Reaction notes
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