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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373454Generated: October 26, 2026

Methanol → HCID 15003636, compound

https://huagongshe.com/reaction/373454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiethyl MaleateHCID 5271566—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Benzylthio-7-fluoro-5-methylthio-1,2,4-triazolo[4,3-c]pyrimidineHCID 15003630—
Reactant2-Benzylthio-7-fluoro-5-methylthio-1,2,4-triazolo[1,5-c]pyrimidineHCID 19809851—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 15003636HCID 1500363656.7%

Reaction Steps

A 25 percent solution of sodium methoxide in methanol (1.9 ml, 0.0085 mol) was added to a solution of 19.9 g (0.065 mol) of 3-benzylthio-7-fluoro-5-methylthio-1,2,4-triazolo[4,3-c]pyrimidine containing a small amount of 2-benzylthio-7-fluoro-5-methylthio-1,2,4-triazolo[1,5-c]pyrimidine and 11.2 g (0.065 mol) of diethyl maleate in 250 ml of ethanol at ambient temperature with stirring and allowed to react for about 1 hour. Acetic acid (4 ml) was then added and the volatiles were removed by evaporation under reduced pressure. The residue was dissolved in methylene chloride and the resulting solution was extracted with water, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The residue was triturated with hexane, filtered, and dried to obtain 10.7 g of the title compound as a white powder melting at 121°-122° C. The nmr and uv spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05163995
Source datasetuspto-grants-1992_11
ORD IDord-7a6e954f279e44d4b9354a070500921b
Source noteuspto-grants-1992_11