Hydrochloric Acid → HCID 68412119, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=[O:12])[CH:8]([NH:13]C(=O)C)[CH2:7]2.[ClH:17]>>[ClH:17].[ClH:17].[NH2:13][CH:8]1[CH2:7][C:6]2[C:11](=[C:2]([NH2:1])[CH:3]=[CH:4][CH:5]=2)[NH:10][C:9]1=[O:12]Participants
3
Conditions
- Temperature
- 110 °C
Procedure
N-(8-Amino-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)acetamide (8.4 g) was added to concentrated hydrochloric acid (84 mL), and the mixture was heated at 110° C. for three hours while being stirred, followed by stirring under cooling on ice. The formed precipitates were recovered through filtration, and the thus-obtained solid was washed with ethanol, followed by drying, whereby the title compound (9.17 g) was yielded.
Workup
- stirringby stirring
- temperatureunder cooling on ice
- customThe formed precipitates
- filtrationwere recovered through filtration
- washthe thus-obtained solid was washed with ethanol
- customby drying
Sources & evidence
- ORD record
- ord-65d73bdbd2574308bf8b281452ae0ae2
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08299255B2
Reaction notes
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