Hydrochloric Acid → HCID 70548639, compound
Reaction equation
C([O:3][C:4](=[O:28])[C:5]([CH3:27])([O:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH2:17][CH2:18][CH3:19])[C:12]([C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)=[C:11]2[CH3:26])[CH3:6])C.[ClH:29]>>[ClH:29].[CH3:6][C:5]([O:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH2:17][CH2:18][CH3:19])[C:12]([C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)=[C:11]2[CH3:26])([CH3:27])[C:4]([OH:28])=[O:3]Participants
3
Procedure
The above compound was prepared from 2-methyl-2-[3-methyl-1-propyl-2-(4-pyridyl)-1H-indole-5-yloxy]propanoic acid ethylester by hydrolysis with diluted hydrochloric acid at the boiling temperature. After the hydrochloric acid was distilled off in vacuo, the reaction product was recrystallized from acetone.
Workup
- distillationAfter the hydrochloric acid was distilled off in vacuo
- customthe reaction product was recrystallized from acetone
Sources & evidence
- ORD record
- ord-406739993b464f6e85a11eda7de205f7
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04343811
Reaction notes
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