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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706035Generated: October 27, 2026

Diisopropylamine → HCID 178494157, compound

https://huagongshe.com/reaction/706035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant5-(2-Methoxypyrimidin-5-ylmethyl)-2-thiouracilHCID 21936244—
Reactant4-(4-Fluorophenoxy)benzylchlorideHCID 22293136—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178494157HCID 17849415755.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-((2-methoxypyrimidin-5-yl)methyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (2.75 g, 10.99 mmol), 1-(chloromethyl)-4-(4-fluorophenoxy)benzene (2.6 g, 10.99 mmol) and diisopropylamine (3.34 g, 33.0 mmol) in DCM (50 mL) was heated at 60° C. overnight. After cooling to room temperature, the mixture was washed with brine, the organic phase was dried over Na2SO4, filtered and concentrated to leave the crude product, which was slurred in EA (20 mL) for 10 min, filtered, washed with EA and concentrated in vacuo to afford the title compound (2.75 g, 51.4% yield) as white solid. LCMS: rt=1.47 min, [M+H]=451.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-d0a8a9b126614314b136dacf6d02cb84
Source noteuspto-grants-2015_11