反应详情

温度

0 °C

With stirring, 3.85 g (41.34 mmol) of aniline were added to water (40 ml) and conc. hydrochloric acid (7.07 ml), and this mixture was cooled to 0° C. A solution of 2.85 g (41.34 mmol) of sodium nitrite in water (21 ml) was then added dropwise at between 0° C. and 5° C., followed by stirring at 0° C. for 15 min. Thereafter, at 0° C., a solution of 4.28 g (52.25 mmol) of sodium acetate in water (19 ml) was added rapidly dropwise, and then, with thorough stirring, a solution of 2.73 g (41.34 mmol) of malononitrile in ethanol (10 ml) was added dropwise. After 2 h at 0° C., the resulting precipitate was isolated by filtration with suction and washed three times with water (50 ml each time) and with petroleum ether (50 ml). The residue, still moist, was dissolved in DMF (46 ml) and added dropwise at precisely 85° C. to a solution of 9.5 g (33.07 mmol) of 5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboximidamide acetate (Example 9A) in DMF (46 ml) and triethylamine (5.76 ml). The mixture was then stirred at 100° C. for 4 h and left to cool to RT overnight. The mixture was poured into water (480 ml) and subjected to extractive stirring at RT for 1 h. After the precipitate had been isolated by filtration with suction, it was washed twice with water (100 ml each time) and twice with methanol (50 ml each time) and then dried under a high vacuum.

1. stirringby stirring at 0° C. for 15 min
2. customthe resulting precipitate was isolated by filtration with suction
3. washwashed three times with water (50 ml each time)
4. dissolutionThe residue, still moist, was dissolved in DMF (46 ml)
5. stirringThe mixture was then stirred at 100° C. for 4 h
6. waitleft
7. temperatureto cool to RT overnight
8. stirringto extractive stirring at RT for 1 h
9. customAfter the precipitate had been isolated by filtration with suction, it
10. washwas washed twice with water (100 ml each time) and twice with methanol (50 ml each time)
11. customdried under a high vacuum