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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412907Generated: October 30, 2026

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

https://huagongshe.com/reaction/2412907

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. Mass spectrum: m/e, 241 (P).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495187
Source datasetuspto-grants-1985_01
ORD IDord-69cf0909fdf0440a9287fdc6214bf8c7
Source noteuspto-grants-1985_01