Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 2-Methyl-2-[1,2-dimethyl-3-(4-methyl-phenyl)-1H-indole-5-yloxy]-propanoic acid ethylester

HRID 66848Notes

Reaction equation

HRID 66848 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]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)=[C:3]1[CH3:19].[CH2:20]([O:22][C:23](=[O:28])[C:24](Br)([CH3:26])[CH3:25])[CH3:21]>>[CH2:20]([O:22][C:23](=[O:28])[C:24]([CH3:26])([O:11][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:2]([CH3:1])[C:3]([CH3:19])=[C:4]2[C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)[CH3:25])[CH3:21]

Participants

3

Procedure

The above compound was prepared from 1,2-dimethyl-3-(4-methyl-phenyl)-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester using a procedure analogous to that of Example 10.

Sources & evidence

ORD record
ord-bf0b9e1c790a4db79565bd240823ab95
Source dataset
uspto-grants-1982_08
Patent number
US04343811

Reaction notes

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