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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434638Generated: October 30, 2026

Sodium Carbonate → HCID 20491752, compound

https://huagongshe.com/reaction/434638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantIsoxazole, 4-(chloromethyl)-3,5-dimethyl-HCID 88246—
Reactant5-Chloropyrimidin-2-ol hydrochlorideHCID 12648523—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 20491752HCID 2049175232.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-chloropyrimidin-2-one hydrochloride (0.668 g), 4-chloromethyl-3,5-dimethylisoxazole (0.874 g), anhydrous sodium carbonate (1.272 g) and benzyltrimethylammonium chloride (15 mg) in dimethylformamide (20 ml) was stirred and heated at 90° C. After 2.25 h the reaction mixture was diluted with water (200 ml) and extracted with ethyl acetate (100 ml, 2×50 ml). The combined extracts were washed with water (50 ml) and brine (50 ml), dried (MgSO4) and evaporated to an orange crystalline solid (0.811 g). The solid was subjected to preparative layer chromatography (p.l.c.) on silica developing with chloroform-ethyl acetate (1:1) (two runs). The major band was eluted with chloroform-ethanol (1:1) (three times) to give a cream crystalline solid (0.313 g) which was recrystallised from ethanol to give the title pyrimidone (0.189 g) m.p. 218°-219° C. (Kofler), λmax (EtOH) 225 nm (ε 9,300), 310 nm (ε 2,200) inflection at 245 nm (ε 4,300) νmax (CHBr3) 1677 cm-1 (C=O), (Nujol) 1668 cm-1 (C=O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399140
Source datasetuspto-grants-1983_08
ORD IDord-173a9656d0ca47809ff36414d4e0908e
Source noteuspto-grants-1983_08