Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 54340937, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[C:17]([OH:20])[CH:18]=3)[N:13]([CH2:21][CH2:22][CH3:23])[C:12]=2[CH3:24])=[CH:5][CH:4]=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:20][C:17]1[CH:18]=[C:19]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH2:21][CH2:22][CH3:23])[C:12]([CH3:24])=[C:11]2[CH2:10][CH2:9][C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=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-[2-(4-methoxy-phenyl)-ethyl]-2-methyl-1-propyl-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester.
Sources & evidence
- ORD record
- ord-9131f46e3b78443391f1c83079156f8f
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
Loading…