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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731938Generated: November 2, 2026

Dimethylformamide → 1-Ethyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amine

https://huagongshe.com/reaction/1731938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Chloro-1-ethyl-[1,2,4]triazolo[4,3-a]quinoxalineHCID 13385706—
Product1-Ethyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amineHCID 1338571122%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ammonia gas was bubbled through a solution of 1.2 g. (0.005 mole) of 4-chloro-1-ethyl-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 4) in N,N-dimethylformamide (20 ml.) at 0° C. for about 2 minutes. The solution was stirred at 0° C. for 30 minutes and at room temperature for one hour. The reaction mixture was then poured over ice and stirred for 20 minutes. The precipitate which formed was removed by filtration, washed with water and air dried. Recrystallization from ethanol afforded 220 mg. (22% yield) of pure 4-amino-1-ethyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 284°-8° C. Mass spectrum: m/e, 213 (P).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623725
Source datasetuspto-grants-1986_11
ORD IDord-d56a7d1adac940c39727e124dec8719b
Source noteuspto-grants-1986_11