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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731935Generated: November 1, 2026

Ethylamine → 4-Ethylamino-[1,2,4]triazolo[4,3-a]quinoxaline

https://huagongshe.com/reaction/1731935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-Chloro[1,2,4]triazolo[4,3-a]quinoxalineHCID 1126118—
SolventDimethylformamideHCID 6228—
Product4-Ethylamino-[1,2,4]triazolo[4,3-a]quinoxalineHCID 1338570932%

Reaction Steps

A slurry of 2.0 g. (0.01 mole) of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) in N,N-dimethylformamide (30 ml.) was saturated with monoethylamine gas and stirred at room temperature for 2 hours. Monoethylamine gas was again bubbled through the mixture and stirring was continued for 2 hours. The precipitate was removed by filtration and washed with N,N-dimethylformamide. Recrystallization from methanol afforded 680 mg. (32% yield) 4-ethylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 254°-6° C. Mass spectrum: m/e, 213 (P).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623725
Source datasetuspto-grants-1986_11
ORD IDord-678ae0ed9ab74ee2a1881b5b7d6e3e9e
Source noteuspto-grants-1986_11