Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 54038903, compound
Reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([OH:11])=[CH:8][CH:9]=2)[C:4]([CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[C:3]1[CH3:20].[CH2:21]([O:23][C:24](=[O:29])[C:25](Br)([CH3:27])[CH3:26])[CH3:22]>>[CH2:21]([O:23][C:24](=[O:29])[C:25]([CH3:27])([O:11][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:2]([CH3:1])[C:3]([CH3:20])=[C:4]2[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH3:26])[CH3:22]Participants
3
Procedure
In accordance with a procedure analogous to that of Example 10, the above compound was prepared from 1,2-dimethyl-3-(2-phenyl-ethyl)-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester.
Sources & evidence
- ORD record
- ord-79fc0f2a08a44e96b1d3cc542e6cf519
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
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