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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755911Generated: November 2, 2026

Pyridine → HCID 178498585, compound

https://huagongshe.com/reaction/1755911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178498587HCID 178498587—
SolventDichloromethaneHCID 6344—
ProductHCID 178498585HCID 17849858540.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

Methyl 4,7-dihydro-2-(hydroxymethyl)-7-oxo-s-triazolo[1,5-a]pyrimidine-5-carboxylate (2.5 g) (11.1 mmol) are suspended in 20 ml of dichloromethane. After the addition of 1.76 g (22.3 mmol) of pyridine and 2.27 g (22.2 mmol) of acetic anhydride the mixture is stirred at 55° C. for 8 hours. The mixture is concentrated in a vacuum and the product is precipitated with diethyl ether. After recrystallization from methanol there are obtained 1.2 g of methyl 2-(acetoxymethyl)-4,7-dihydro-7-oxo-s-triazolo[1,5-a]pyrimidine-5-carboxylate as white crystals of melting point 260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438052
Source datasetuspto-grants-1995_08
ORD IDord-806e1a45304f4eba80f593513216625c
Source noteuspto-grants-1995_08