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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802190Generated: October 31, 2026

Ethoxalyl chloride → Ethyl 7-bromo-(1,2,4)triazolo(1,5-a)pyridine-2-carboxylate

https://huagongshe.com/reaction/1802190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
Reactant1,2-Diamino-4-bromo-pyridinium 2,4,6-trimethyl-benzenesulfonateHCID 86666016—
SolventPyridineHCID 1049—
ProductEthyl 7-bromo-(1,2,4)triazolo(1,5-a)pyridine-2-carboxylateHCID 6777463860.5%

Reaction Steps

A mixture of 1,2-diamino-4-bromopyridinium 2,4,6-trimethylbenzenesulfonate (4.18 g, 10.8 mmol) and ethyl 2-chloro-2-oxoacetate (2.4 ml, 21.5 mmol) in pyridine (25 ml) is heated for 18 hours to 100° C. The solvent is evaporated and the orange residue triturated with sat. aqueous sodium hydrogencarbonate solution for 2 hours. The solid is collected by filtration, washed several times with water and dried affording ethyl 7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate (1.759 g, 60.5%) as a light pink solid. mp.: 158-160° C. MS: m/z=270.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-b5a45b56f06e4424b8b79403101c599c
Source noteuspto-grants-2013_01