Reaktion #1584591

Reaktionsgleichung

water

4-chloro-1-(2-cyclopropyl-3-methyl-2H-indazol-5-yl)pyridin-2(1H)-one

[5-(trifluoromethyl)thiophen-3-yl]methanol

potassium tert-butoxide

→

title compound

Ausbeute 83.1%

1-(2-cyclopropyl-3-methyl-2H-indazol-5-yl)-4-{[5-(trifluoromethyl)thiophen-3-yl]methoxy}pyridin-2(1H)-one

Ausbeute 83.1%

Lösungsmittel

DMA

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at an inside temperature of 70° C. for 1.5 hr
2. 2
   workup.STIRRINGthe obtained suspension was stirred overnight
3. 3
   FiltrationThe precipitated solid was collected by filtration
4. 4
   Waschenwashed with water (2.8 L), ethanol (540 ml) and diisopropyl ether (500 ml)

Vorschrift

To a solution of [5-(trifluoromethyl)thiophen-3-yl]methanol (100 g) in DMA (1363 ml) was added potassium tert-butoxide (61.3 g) at 5° C., and the mixture was stirred at the same temperature for 30 min. To the obtained mixture was added 4-chloro-1-(2-cyclopropyl-3-methyl-2H-indazol-5-yl)pyridin-2(1H)-one (136.5 g), and the mixture was stirred at an inside temperature of 70° C. for 1.5 hr. The reaction mixture was cooled to room temperature, water (1.4 L) was added, and the obtained suspension was stirred overnight. The precipitated solid was collected by filtration, and washed with water (2.8 L), ethanol (540 ml) and diisopropyl ether (500 ml) to give the title compound (168.6 g).

Quelle