Hydrochloric Acid → HCID 59828247, compound
Reaction equation
[O:1]=[C:2]1[C:7]([C:8]([O:10]CC)=O)=[CH:6][CH:5]=[C:4]([C:13]([F:19])([F:18])[C:14]([F:17])([F:16])[F:15])[NH:3]1.Cl>CC(N)CC>[CH3:13][CH:4]([NH:3][C:8]([C:7]1[C:2](=[O:1])[NH:3][C:4]([C:13]([F:18])([F:19])[C:14]([F:15])([F:16])[F:17])=[CH:5][CH:6]=1)=[O:10])[CH2:5][CH3:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
At room temperature, 160 mg (0.56 mmol) of ethyl 2-oxo-6-(pentafluoroethyl)-1,2-dihydropyridine-3-carboxylate were stirred in 5 ml of 2-butylamine for 14 h. The pH was then adjusted to 2 by addition of 1N hydrochloric acid, which resulted in the precipitation of a colorless solid. Filtration with suction and drying gave 160 mg (91% of theory) of the product.
Workup
- customresulted in the precipitation of a colorless solid
- filtrationFiltration with suction
- customdrying
- customgave 160 mg (91% of theory) of the product
Sources & evidence
- ORD record
- ord-26c182cdde4e4eb4a9aae8e535865349
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102623B2
Reaction notes
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