Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 2-[3-(4-Fluoro-phenyl)-1-hexyl-2-methyl-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([OH:17])[CH:15]=3)[N:10]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:9]=2[CH3:24])=[CH:4][CH:3]=1.[CH2:25]([O:27][C:28](=[O:33])[C:29](Br)([CH3:31])[CH3:30])[CH3:26]>>[CH2:25]([O:27][C:28](=[O:33])[C:29]([O:17][C:14]1[CH:15]=[C:16]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[C:9]([CH3:24])=[C:8]2[C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=1)([CH3:31])[CH3:30])[CH3:26]Participants
3
Procedure
In accordance with a procedure analogous to that of Example 10, the above compound was prepared from 3-(4-fluoro-phenyl)-1-hexyl-2-methyl-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester.
Sources & evidence
- ORD record
- ord-8f4fd94553d646d78eaabadebcb513e6
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
Loading…