Acetamide → 5-Bromo-7-ethylindoline-2,3-dione
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:13])[CH:10]=NO)=[C:4]([CH2:14][CH3:15])[CH:3]=1.C(N)(=[O:18])C>>[Br:1][C:2]1[CH:7]=[C:6]2[C:5](=[C:4]([CH2:14][CH3:15])[CH:3]=1)[NH:8][C:9](=[O:13])[C:10]2=[O:18]Participants
3
Procedure
Following the procedure of example 36.B. except using N-(4-Bromo-2-ethyl-phenyl)-2-hydroxyimino-acetamide as the acetamide component afforded the title compound as a solid. ESI (−) MS m/e=252 (MH−).
Sources & evidence
- ORD record
- ord-8bb24b8c0c7a4715bec27885249914e8
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446122B2
Reaction notes
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