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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263088Generated: November 3, 2026

Pyridine → 2,2,2-Trichloroethyl [2-(acetylamino)pyrimidin-5-yl]carbamate

https://huagongshe.com/reaction/2263088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantN-(5-aminopyrimidin-2-yl)acetamideHCID 20387481—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trichloroethyl [2-(acetylamino)pyrimidin-5-yl]carbamateHCID 866254949.1%

Reaction Steps

To a solution of N-(5-aminopyrimidin-2-yl)acetamide (450 mg, 2.96 mmol) and pyridine (0.718 ml, 8.87 mmol) in tetrahydrofuran (10 ml) was added 2,2,2-trichloroethyl chloroformate (0.612 ml, 4.44 mmol) with ice-cooling, the mixture was stirred for 1 hour with ice-cooling and then at room temperature for 2 hours, the reaction mixture was poured into ice-water and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure to obtain the desired product (88.3 mg, 9.1%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-5a2bd0324af9492eb9f6340a258a7f9f
Source noteuspto-grants-2010_12