Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 54402430, compound
Reaction equation
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([OH:11])[CH:9]=2)[N:4]([CH2:12][CH2:13][CH3:14])[C:3]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[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:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[N:4]([CH2:12][CH2:13][CH3:14])[C:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[C:2]2[CH3:1])[CH3:26])[CH3:22]Participants
3
Procedure
The above compound was prepared from 3-methyl-2-phenyl-1-propyl-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-13e4adb0620b4a3e9e0786af3c31f7d9
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
Loading…