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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755902Generated: October 31, 2026

Methyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylate → HCID 178499051, compound

https://huagongshe.com/reaction/1755902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylateHCID 19917996—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventMethanolHCID 887—
ProductHCID 178499051HCID 17849905190.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 5-(acetoxymethyl)-7-chloro-s-triazolo[1,5-a]pyrimidine-2-carboxylate (380 mg) (1.33 mmol) are dissolved in 20 ml of methanol. After the addition of 296 mg (4 mmol) of sodium hydrogen sulphide monohydrate the mixture is stirred at 60° C. for 5 hours. The reaction mixture is concentrated and brought to pH 3 with dilute aqueous hydrochloric acid. The product is filtered off under suction, washed with water/methanol and crystallized from methanol. There are obtained 290 mg of methyl 5-(hydroxymethyl)-7-mercapto-s-triazolo[1,5-a]pyrimidine-2-carboxylate as a brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438052
Source datasetuspto-grants-1995_08
ORD IDord-d323a83161a3431cb5431896bd4748b5
Source noteuspto-grants-1995_08