Hydrochloric Acid → HCID 14627260, compound
Reaction equation
C([NH:4][C:5]1(C(OCC)=O)[CH2:14][C:13]2[C:8](=[C:9]([CH3:15])[CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=[O:16])(=O)C.[ClH:22]>>[ClH:22].[NH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[C:9]([CH3:15])[CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=[O:16]Participants
3
Procedure
To 2.7 g of ethyl 3-acetylamino-8-methyl-3,4-dihydrocarbostyril-3-carboxylate was added 60 ml of 20%-hydrochloric acid, then the mixture was refluxed by heating for 2 hours. The solvent was removed by evaporation, then water was removed by azetropic distillation with ethanol. The residue thus obtained was recrystallized from methanol-diethyl ether to obtain 1.74 g of 3-amino-8-methyl-3,4-dihydrocarbostyril hydrochloride. Colorless flake-like crystals. Melting point: Over 300° C.
Workup
- temperaturethe mixture was refluxed
- temperatureby heating for 2 hours
- customThe solvent was removed by evaporation
- customwater was removed by azetropic distillation with ethanol
- customThe residue thus obtained
- customwas recrystallized from methanol-diethyl ether
Sources & evidence
- ORD record
- ord-1524071431cc4503975ddcac3cd3b31e
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05358949
Reaction notes
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