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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755907Generated: October 30, 2026

Methyl 7-chloro-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine-5-carboxylate → HCID 178498634, compound

https://huagongshe.com/reaction/1755907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 7-chloro-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine-5-carboxylateHCID 14852618—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventMethanolHCID 887—
ProductHCID 178498634HCID 17849863483.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 7-chloro-2-methyl-s-triazolo[1,5-a]pyrimidine-5-carboxylate (0.80 g) (3.53 mmol) are suspended in 35 ml of methanol and treated with 0.78 g (10.6 mmol) of sodium hydrogen sulphide hydrate. After stirring at 60° C. for 5 hours the mixture is concentrated and the residue is dissolved in 20 ml of water. The solution is acidified to pH 3 with 3N aqueous hydrochloric acid. The precipitated product is filtered off under suction and washed with water and methanol. After recrystallization from methanol/dichloromethane there is obtained 0.66 g of methyl 7-mercapto-2-methyl-s-triazolo[1,5-a]pyrimidine-5-carboxylate as yellow crystals of melting point 237° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438052
Source datasetuspto-grants-1995_08
ORD IDord-09567eebbc3546739268131d09b09d0d
Source noteuspto-grants-1995_08