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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422240Generated: November 1, 2026

2-Methylaziridine → N-(2,3-dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-2-methylaziridine

https://huagongshe.com/reaction/1422240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylaziridineHCID 6377—
ReactantTetrabutylammonium HydroxideHCID 2723671—
Reactant5-Bromomethyl-7-nitro-2,3-dimethoxyquinoxalineHCID 23297983—
SolventDichloromethaneHCID 6344—
ProductN-(2,3-dimethoxy-7-nitro-quinoxalin-5-ylmethyl)-2-methylaziridineHCID 18706571—

Reaction Steps

200 mg (0.61 mmol) of 5-bromomethyl-2,3-dimethoxy-7-nitro-quinoxaline, 0.086 ml (2 equiv.) of propyleneimine and 0.295 ml (0.3 equiv.) of an aqueous 40% tetrabutylammonium hydroxide solution are stirred in 8 ml of dichloromethane for 20 hours at room temperature. The mixture is concentrated by evaporation and the residue is extracted with ethyl acetate and a 5% sodium carbonate solution. The combined organic phases are washed once with brine, dried over magnesium sulfate and concentrated by evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080743
Source datasetuspto-grants-2000_06
ORD IDord-f364f529c1054243a41dc138abe5b97d
Source noteuspto-grants-2000_06