Hydrazine → 4-(6-Bromo-7-methyl-2-oxo-2,3-dihydro-indol-1-ylmethyl)-n,n-dimethyl-benzenesulfonamide
Reaction equation
[Br:1][C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([C:6](=O)[C:7](=[O:25])[N:8]2[CH2:12][C:13]2[CH:18]=[CH:17][C:16]([S:19]([N:22]([CH3:24])[CH3:23])(=[O:21])=[O:20])=[CH:15][CH:14]=2)=[CH:4][CH:3]=1.NN>>[Br:1][C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([CH2:6][C:7](=[O:25])[N:8]2[CH2:12][C:13]2[CH:18]=[CH:17][C:16]([S:19]([N:22]([CH3:24])[CH3:23])(=[O:21])=[O:20])=[CH:15][CH:14]=2)=[CH:4][CH:3]=1Participants
3
Procedure
Following the same procedure as described in example 10C, 4-(6-bromo-7-methyl-2,3-dioxo-2,3-dihydro-indol-1-ylmethyl)-N,N-dimethyl-benzenesulfonamide (0.392 g, 0.895 mmol) was treated with hydrazine to provide the crude title compound of 12B.
Sources & evidence
- ORD record
- ord-22982c8bddc34733b1ea4d73037a91a8
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586447B1
Reaction notes
Loading…