Реакция #155332

Уравнение реакции

hydrochloric acid ethyl acetate

tert-butyl 4-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]acetylamino}piperidine-1-carboxylate

→

2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]-N-piperidin-4-ylacetamide

Выход 27.5%

Растворители

ethanol

Условия реакции

Обработка

1. 1
   КонцентрированиеThe resulting mixture was concentrated under reduced pressure
2. 2
   workup.ADDITIONAfter adding an aqueous sodium bicarbonate solution to the residue
3. 3
   Промывкаthe residue was washed with ethyl acetate
4. 4
   workup.ADDITIONA 2N aqueous sodium hydroxide solution was added to the water layer
5. 5
   Экстракцияfollowed by extraction
6. 6
   ПромывкаThe thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution
7. 7
   Сушкаdried over anhydrous magnesium sulfate
8. 8
   Концентрированиеconcentrated under reduced pressure
9. 9
   ДругоеThe residue was recrystallized from ethanol-ethyl acetate

Методика

A 4N hydrochloric acid ethyl acetate solution (25 ml) was added to an ethanol solution (12 ml) of tert-butyl 4-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]acetylamino}piperidine-1-carboxylate (820 mg, 1.44 mmol), followed by stirring at room temperature for 28 hours. The resulting mixture was concentrated under reduced pressure. After adding an aqueous sodium bicarbonate solution to the residue to adjust the pH to 8, the residue was washed with ethyl acetate. A 2N aqueous sodium hydroxide solution was added to the water layer to adjust its pH to 11, followed by extraction using dichloromethane. The thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was recrystallized from ethanol-ethyl acetate, giving a white powder of 2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]-N-piperidin-4-ylacetamide (185 mg, yield: 27%).

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