Water → N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridine carboxamide (50 g), potassium fluoride (30.85.g), cyclopropylamine (40.43 g) were suspended in o-xylene (150 ml) and heated to 130-140° C. in autoclave for 5-8 h. Then the reaction mass was cooled to 25-30° C., diluted with o-xylene (250 ml) and further heated the reaction mass to 70-75° C. Thereafter, DM water (150 ml) added and stirred for 10 min at 70-75° C. The aqueous layer was separated at hot condition and organic layer was washed with DM water (150 ml) at 70-75° C. and organic layer was concentrated at 60-63° C. under reduced pressure up to residual weight attained is approximately 200 g. The concentrated mass was cooled to 25-30° C. and stirred for 15 min and further cooled to 5-10° C. and stirred for 30 min. Filtered the solid obtained and washed with chilled o-xylene (50 ml, 5-10° C.). Dried the obtained solid at 45-50° C. under reduced pressure.

Herkunft & Nachweise