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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464290Generated: October 29, 2026

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

https://huagongshe.com/reaction/464290

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°-158° C. Mass spectrum: m/e, 241 (P).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547501
Source datasetuspto-grants-1985_10
ORD IDord-a44d5a4681ad487292fa1eb849e8aa9d
Source noteuspto-grants-1985_10