Water → 6-Chloropyridazine-3-carbonitrile

A mixture of 6-chloropyridazine-3-carboxamide (described in reference example 3) (15 g, 95.5 mmol) and pyridine (22.6 g, 23.1 ml, 286.6 mmol) were was suspended in dichloromethane and cooled to −30 ° C. under argon. TFAA was added dropwise to the stirred mixture keeping the internal temperature below −20 ° C. The reaction was stirred for 19.5 hours allowing to warm to ambient temperature. The mixture was poured into water(500 ml) and washed with water (4×500 ml) until the aqueous phase was pale yellow. The organic phase was dried over MgSO4, filtered through a pad of silica (50mm diameter, 30mm deep), and concentrated in vacuo. The resulting solid was purified by MPLC (40% dichloromethane/20%ethyl acetate/hexane) to give 3-chloro-6-cyanopyridazine as a colourless solid (5.25 g, 59%).

1. customthe internal temperature below −20 ° C
2. temperatureto warm to ambient temperature
3. washwashed with water (4×500 ml) until the aqueous phase
4. dry with materialThe organic phase was dried over MgSO4
5. filtrationfiltered through a pad of silica (50mm diameter, 30mm deep)
6. concentrationconcentrated in vacuo
7. customThe resulting solid was purified by MPLC (40% dichloromethane/20%ethyl acetate/hexane)

ORD 기록

ord-eba15fd14e384df78c28c90268558d30

출처 데이터셋

uspto-grants-2002_04

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06365603B1