HRID368503
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To 5 ml of acetic acid was added 260 mg of ethyl 1-(6-amino-3,5-difluoropyridine-2-yl)-5-benzylamino-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate together with 50 mg of 10% palladium on carbon, and the mixture was hydrogenated at room temperature for 4 hours. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. The procedure of adding 10 ml of ethanol to the residue and concentrating under reduced pressure was repeated twice. The precipitate was dispersed in ethanol, collected by filtration, and washed with ethanol and diisopropylether successively to obtain 160 mg of the title compound as a pale yellow powder.
WORKUP
后处理
- customThe catalyst was separated by filtration
- distillationthe solvent and the like were distilled off under reduced pressure
- additionThe procedure of adding 10 ml of ethanol to the residue
- concentrationconcentrating under reduced pressure
- additionThe precipitate was dispersed in ethanol
- filtrationcollected by filtration
- washwashed with ethanol and diisopropylether successively