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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731940Generated: November 1, 2026

Dimethylamine → 1-ethyl-N,N-dimethyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amine

https://huagongshe.com/reaction/1731940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant4-Chloro-1-ethyl-[1,2,4]triazolo[4,3-a]quinoxalineHCID 13385706—
SolventDimethylformamideHCID 6228—
Product1-ethyl-N,N-dimethyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amineHCID 89929542%

Reaction Steps

4-Chloro-1-ethyl-[1,2,4]triazolo-[4,3-a]quinoxaline (1.2 g., 0.005 mole), the product of Example 4, and 676 mg. (0.015 mole) of anhydrous dimethylamine in N,N-dimethylformamide (50 ml.) were stirred at 0° C. for 30 minutes and at room temperature for 2 hours. The reaction mixture was poured over ice and stirred for 20 minutes. The precipitate which formed was separated by filtration, washed with water and air dried. Recrystallization from chloroform and then from chloroform/cyclohexane afforded 510 mg. (42% yield) of 4-dimethylamino-1-ethyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 155°-8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623725
Source datasetuspto-grants-1986_11
ORD IDord-f438f51f835b4a998c6c758a71ce919f
Source noteuspto-grants-1986_11