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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159681Generated: November 3, 2026

4-Fluorobenzylic alcohol → HCID 59514509, compound

https://huagongshe.com/reaction/1159681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzylic alcoholHCID 68022—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59514548HCID 59514548—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59514509HCID 5951450942%

Reaction Steps

A mixture of methyl (4-(dimethylamino)-2-{4-[(phenoxycarbonyl)amino]benzyl}pyrimidin-5-yl)acetate (100 mg, 0.24 mmol) and 4-fluorobenzyl alcohol (60 mg, 0.48 mmol) in N,N-diisopropylethylamine (0.17 mL, 0.95 mmol) and tetrahydofuran (2 mL) was refluxed for 24 hours. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure and the remaining residue was purified by preparative TLC (chloroform/methanol 30:1) to give methyl {4-(dimethylamino)-2-[4-({[(4-fluorobenzyl)oxy]carbonyl}amino)benzyl]pyrimidin-5-yl}acetate (45 mg, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812160B2
Source datasetuspto-grants-2010_10
ORD IDord-847c72c783594047842525962c9bd493
Source noteuspto-grants-2010_10