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HRID 2088676Erstellt: 26. Oktober 2026

Water → tert-Butyl 4-[7-(2,4-dichlorophenyl)-5-oxo-5,6-dihydro [1,2,4]triazolo[1,5-c]pyrimidin-2-yl]-piperidine-1-carboxylate

https://huagongshe.com/reaction/2088676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCalcium ChlorideHCID 5284359—
Edukttert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
EduktEthyl[2-cyano-1-(2,4-dichlorophenyl)ethenyl]carbamateHCID 76754608—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkttert-Butyl 4-[7-(2,4-dichlorophenyl)-5-oxo-5,6-dihydro [1,2,4]triazolo[1,5-c]pyrimidin-2-yl]-piperidine-1-carboxylateHCID 136104185—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

In a round-bottom flask fitted with reflux condenser and a drying tube filled with calcium chloride, 5.86 g (20.6 mmol) of ethyl[2-cyano-1-(2,4-dichlorophenyl)ethenyl]carbamate and 5.00 g (20.6 mmol) of tert-butyl 4-(hydrazinylcarbonyl)piperidine-1-carboxylate were dissolved in 11 ml of 1-methyl-2-pyrrolidone, and the reaction mixture was stirred at 150° C. for 3 h. The reaction solution was cooled to RT, water (150 ml) was added and the mixture was stirred in an ultrasonic bath for another 2 min. The solid was filtered off with suction and dried under high vacuum. This gave 7.23 g (76% of theory) of the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436003B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-0c2b4895ab8e4f2fa572acd5025e5da4
Quellennotizuspto-grants-2013_05