5-acetyl-1-ethoxycarbonyl-2,3-dihydro-1H-indole → 5-bromoacetyl-1-ethoxycarbonyl-2,3-dihydro-1H-indole
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:8][CH2:7]2)(=[O:3])[CH3:2].[Br:18]CC(C1C=C2C(=CC=1)CCC2)=O>>[Br:18][CH2:2][C:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:8][CH2:7]2)=[O:3]Participants
3
Procedure
*5-bromoacetyl-1-ethoxycarbonyl-2,3-dihydro-1H-indole was prepared from 5-acetyl-1-ethoxycarbonyl-2,3-dihydro-1H-indole (Y. Ishihara et al., J.Chem.. Soc. Perkin Trans.1, 1992, 3401) according to the procedure for preparing 5-bromoacetylindan described in Example 11.
Sources & evidence
- ORD record
- ord-0faa428d2ebc4c4e8e7e0d0b6be7b28e
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06303628B1
Reaction notes
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