Réaction #72011

Équation de réaction

Ethyl acetate

cis(±)-4-chloro-N-(3-ethoxypiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamide hydrochloride

(1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydroquinolin-3-yl)carbonyl difluoroborate

→

title compound

Rendement 62.0%

cis(±)-7-(4-{[(4-Chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-ethoxypiperidin-1-yl)-1-cyclopropyl-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Rendement 62.0%

Solvants

Triethylamine

triethylamine

water

Ethanol

DMSO

Conditions de réaction

Traitement

1. 1
   Lavagethe organic layer was washed with saturated aqueous sodium bicarbonate solution
2. 2
   Séchagedried over anhydrous sodium sulfate
3. 3
   Concentrationconcentration under reduced pressure
4. 4
   workup.STIRRINGthe mixture was stirred at 80° C. for six hours
5. 5
   TempératureThe reaction solution was cooled to room temperature
6. 6
   FiltrationThe resulting solid was collected by filtration
7. 7
   Lavagewashed with ethanol

Mode opératoire

Ethyl acetate was added to cis(±)-4-chloro-N-(3-ethoxypiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamide hydrochloride obtained in Example (131a) (100 mg, 0.297 mmol), and the organic layer was washed with saturated aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue and (1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydroquinolin-3-yl)carbonyl difluoroborate obtained in Example (146a) (82 mg, 0.30 mmol) were dissolved in DMSO (0.6 mL). Triethylamine (0.100 mL, 0.721 mmol) was added, and the mixture was stirred at 40° C. overnight. Ethanol (3 mL), water (0.3 mL) and triethylamine (0.3 mL) were added to the reaction solution, and the mixture was stirred at 80° C. for six hours. The reaction solution was cooled to room temperature. The resulting solid was collected by filtration and washed with ethanol to obtain 102.5 mg of the title compound as a pale yellow solid (62%).

Source