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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470307Generated: October 27, 2026

Benzyl Chloride → Ethyl 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1470307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantTriethylamineHCID 8471—
ReactantHCID 178469810HCID 178469810—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylateHCID 6746048242%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylate, 3-a, (0.62 g, 2.7 mmol) in DMF (7 ml) were added benzyl chloride (0.5 g, 3.99 mmol) and Et3N (0.8 g, 7.97 mmol). The resulting mixture was then heated at 60° C. for 12 hours. Then the mixture was cooled to room temperature and diluted with water followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated under vacuum. The residue was purified on silica gel column with the eluent of ethyl acetate/petroleum ether=1/1 (Rf=0.7) to afford the compound, 3-b, (0.36 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006433B2
Source datasetuspto-grants-2015_04
ORD IDord-c225ff1bc3e1456a9679bbc72fb2531f
Source noteuspto-grants-2015_04