Pyridine → 2-Amino-6-chloropyridine-3-carbonitrile

Temperatur

0 °C

11.15 g (53.6 mmol) of 2-amino-6-chloropyridine-3-carbaldehyde oxime hydrochloride (Example 27A) were initially charged in dioxane, 13 ml (161 mmol) of pyridine were added and the mixture was cooled to 0° C. 8.3 ml (58.95 mmol) of trifluoroacetic anhydride were added, and the reaction was warmed to RT and then stirred at 60° C. for 2 h. The reaction mixture was taken up in a mixture of ethyl acetate and sodium bicarbonate solution. The organic phase was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated on a rotary evaporator. The residue was suspended in dichloromethane:diethyl ether 3:1, and the solid was filtered off with suction and dried. This gave 5.56 g (66% of theory) of the product as a solid.

1. temperaturethe reaction was warmed to RT
2. washThe organic phase was washed with saturated aqueous sodium chloride solution
3. dry with materialdried over magnesium sulfate
4. concentrationconcentrated on a rotary evaporator
5. filtrationthe solid was filtered off with suction
6. customdried

ORD-Eintrag

ord-b64671c2b5694f00acfa2cdc97cdcd23

Quelldatensatz

uspto-grants-2013_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08476267B2