Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 54141958, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[C:8]3[N:9]([CH:16]=[C:17]([OH:19])[CH:18]=3)[C:10]3[C:15]=2[CH2:14][CH2:13][CH2:12][CH:11]=3)=[CH:3][CH:2]=1.[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]([O:19][C:17]1[CH:18]=[C:8]2[C:7]([C:4]3[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=3)=[C:15]3[C:10](=[CH:11][CH2:12][CH2:13][CH2:14]3)[N:9]2[CH:16]=1)([CH3:26])[CH3:25])[CH3:21]Participants
3
Procedure
The above compound was prepared from 7,8-dihydro-9-(4-pyridyl)-6H-pyrrolo[1,2-a]-indole-2-ol and 2-bromo-2-methyl-propanoic acid ethylester using a procedure analogous to that of Example 10.
Sources & evidence
- ORD record
- ord-22fa6106f0b24b2cb7f5336871c5a6fc
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
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