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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755913Generated: October 29, 2026

2-Acetoxymethyl7-chloro-5-methoxycarbonyl-s-triazolo[1,5-a]pyrimidine → HCID 178498635, compound

https://huagongshe.com/reaction/1755913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Acetoxymethyl7-chloro-5-methoxycarbonyl-s-triazolo[1,5-a]pyrimidineHCID 15672766—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventMethanolHCID 887—
ProductHCID 178498635HCID 17849863598.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 2-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-5-carboxylate (370 mg) (1.3 mmol) are dissolved in 10 ml of methanol. After the addition of 289 mg (3.9 mmol) of sodium hydrogen sulphide hydrate the mixture is stirred at 60° C. for 4 hours. The yellow solution is concentrated in a vacuum. The residue is dissolved in water and the product is precipitated at pH 3 with 3N aqueous hydrochloric acid. The precipitate is filtered off under suction and crystallized from methanol. There are obtained 360 mg of methyl 2-(acetoxymethyl)-7-mercapto-s-triazolo[1,5-a]pyrimidine-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438052
Source datasetuspto-grants-1995_08
ORD IDord-acea53ddaf2c42c282e9444685db86f8
Source noteuspto-grants-1995_08