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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742561Generated: November 2, 2026

Malic Acid → HCID 19006685, compound

https://huagongshe.com/reaction/1742561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalic AcidHCID 525—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 19006688HCID 19006688—
ReactantHCID 20087472HCID 20087472—
ReactantHCID 136169458HCID 136169458—
SolventDichloromethaneHCID 6344—
SolventMethyl Ethyl KetoneHCID 6569—
SolventPotassium CarbonateHCID 11430—
ProductHCID 19006685HCID 19006685—

Reaction Steps

A solution of 0.1 mol of 5-heptyloxy-2-(4-(2-hydroxy-5-oxaoctyloxy)-2-fluorophenyl)pyrimidine (prepared by heating optically active 1,2-epoxy-5-oxaoctane, obtainable from malic acid, with 5-heptyloxy-2-(4-hydroxy-2-fluorophenyl)pyrimidine in the presence of dry potassium carbonate and methyl ethyl ketone as solvent) in methylene chloride is cooled to -40° C. and 0.11 mol of DAST is added to it dropwise with moisture being excluded. The reaction mixture is then stirred for 12 hours while heating slowly to room temperature. Then hydrolysis is carried out with ice cooling and the reaction mixture is washed with dilute sodium hydroxide solution and several times with water. After drying over magnesium sulfate, the solvent is removed on a rotary evaporator and the crude product is purified chromatographically and by crystallization. Optically active 5-heptyloxy-2-(4-(2-fluoro-5-oxaoctyloxy)-2-fluorophenyl)pyrimidine is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05340497
Source datasetuspto-grants-1994_08
ORD IDord-774950b6f0b44f8fae5b098ca217b904
Source noteuspto-grants-1994_08