Iodoethane → (+/-)-Ethyl (3-ethyl-4-nitro-2-oxo-2,3-dihydro-1H-indol-3-yl)acetate
Reaction equation
[CH3:1][C:2]1([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-:13])=[O:12])[NH:4][C:3]1=[O:14].I[CH2:22]C>>[CH2:1]([C:2]1([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-:13])=[O:12])[NH:4][C:3]1=[O:14])[CH3:22]Participants
3
Procedure
Essentially following the procedures described for Intermediate 16, but using iodoethane in place of iodomethane, the title compound was prepared. MS: m/z=293 (M+1).
Sources & evidence
- ORD record
- ord-7d6656f9202a473a97d6800e0cde57a4
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07968540B2
Reaction notes
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