Hydrochloric Acid → HCID 16218315, compound
Reaction equation
C([NH:4][CH:5]([CH2:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][C:12](=[O:20])[CH:11]=1)[C:6]([OH:8])=[O:7])(=[O:3])C.[ClH:21]>>[OH2:3].[ClH:21].[NH2:4][CH:5]([CH2:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][C:12](=[O:20])[CH:11]=1)[C:6]([OH:8])=[O:7]Participants
3
Procedure
To 2.7 g of 2-acetylamino-3-(2-quinolon-4-yl)propionic acid was added 30 ml of 20%-hydrochloric acid and the mixture was refluxed for 3 hours. The reaction mixture was concentrated under a reduced pressure to dryness, the residue obtained was recrystallized from ethanol-water to obtain 1.9 g of 2-amino-3-(2-quinolon-4-yl)propionic acid hydrochloride hydrate in the form of colorless prism-like crystals.
Workup
- temperaturethe mixture was refluxed for 3 hours
- concentrationThe reaction mixture was concentrated under a reduced pressure to dryness
- customthe residue obtained
- customwas recrystallized from ethanol-water
Sources & evidence
- ORD record
- ord-86124a456f104e8db5e41a81d90f9862
- Source dataset
- uspto-grants-1986_03
- Patent number
- US04578381
Reaction notes
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