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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470303Generated: October 27, 2026

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

https://huagongshe.com/reaction/1470303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178524762HCID 178524762—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylateHCID 67459462—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylic acid, 2-c, (1 g, 4.85 mmol) in DMF (40 ml) was added K2CO3 (2.34 g, 16.98 mmol) and benzyl bromide (1.83 g, 10.67 mmol). The mixture was heated at 70° C. for 16 hours. The solution was then cooled to room temperature and diluted with water followed by extraction with ethyl acetate. The combined organic layer was washed with water, dried over sodium sulfate and concentrated under vacuum to provide the crude product, 2-d, as a solid (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006433B2
Source datasetuspto-grants-2015_04
ORD IDord-6afbb78f902c4bcc86e2da876f358fc6
Source noteuspto-grants-2015_04