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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412884Generated: November 2, 2026

Ethyl orthoformate → 4,7-Dimethoxy-[1,2,4]triazolo[4,3-a]quinoxaline

https://huagongshe.com/reaction/2412884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant3,6-Dimethoxy-2-hydrazinoquinoxalineHCID 13385675—
Product4,7-Dimethoxy-[1,2,4]triazolo[4,3-a]quinoxalineHCID 13385692—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture consisting of 1.5 g. (0.068 mole) of 3,6-dimethoxy-2-hydrazinoquinoxaline and 20 ml. of triethylorthoformate was heated with mechanical stirring in a preheated oil bath at 100° C. overnight (~16 hours). The resulting mixture was then cooled to room temperature, and the precipitate which formed was subsequently recovered by means of suction filtration and washed with ethanol to ultimately afford 1.8 g. of pure 4,7-dimethoxy-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 238°-240° C. (decomp.). Mass Spectrum: m/e, 230 (P); m/e, 231 (P+1); m/e, 232 (P+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495187
Source datasetuspto-grants-1985_01
ORD IDord-e515ae203fd4402abc4581d689e149ca
Source noteuspto-grants-1985_01