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HRID 2088674Erstellt: 24. Oktober 2026

Phosphorus oxychloride → 5-Chloro-7-(2,4-dichlorophenyl)-2-[1-(propan-2-yl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidine

https://huagongshe.com/de/reaction/2088674

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
EduktSodium BicarbonateHCID 516892—
Edukt7-(2,4-Dichlorophenyl)-2-[1-(1-methylethyl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-oneHCID 136104184—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
Produkt5-Chloro-7-(2,4-dichlorophenyl)-2-[1-(propan-2-yl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidineHCID 58305977—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

530 mg (1.30 mmol) of 7-(2,4-dichlorophenyl)-2-[1-(1-methylethyl)piperidin-4-yl][1,2,4]-triazolo[1,5-c]pyrimidin-5(6H)-one were initially charged in phosphorus oxychloride (16 ml), and 1.19 g (5.22 mmol) of benzyltriethylammonium chloride were added. The mixture was then stirred at 120° C. for 2.5 h. The reaction mixture was poured onto saturated aqueous sodium bicarbonate solution (150 ml), and solid sodium bicarbonate was added until a pH of 7 had been reached. The mixture was extracted with dichloromethane (3×50 ml), and the combined organic phases were washed with water (50 ml), dried over magnesium sulfate and concentrated. This gave 502 mg (89% of theory) of the product as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436003B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-5e3c396978ab475f8103556eab6cfa93
Quellennotizuspto-grants-2013_05