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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953777Generated: November 2, 2026

Acetaldehyde → Dimethyl N-(7-Nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-aminoethylphosphonate

https://huagongshe.com/reaction/1953777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxalineHCID 17915296—
ReactantDimethylphosphiteHCID 21884954—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductDimethyl N-(7-Nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-aminoethylphosphonateHCID 23297975—

Reaction Steps

500 mg (1.9 mmol) of 5-aminomethyl-7-nitro-2,3-dimethoxyquinoxaline, 834 mg (3.7 eq.) of magnesium sulfate, 335 mg (1.3 eq.) of potassium carbonate and 0.214 ml (2 eq.) of acetaldehyde are stirred at room temperature for 7 hours in 15 ml of dichloromethane. The reaction mixture is filtered off and the filtrate is evaporated. A solution of 0.32 ml (1.2 eq.) of triethylamine, 0.182 ml of dimethyl phosphite and 0.36 ml (1.5 eq.) of trimethylchlorosilane in 10 ml of dichloromethane is stirred at 0° for one hour, and the residue is added to 10 ml of dichloromethane and stirred for 14 hours. Water is added to the reaction mixture and the organic phase is separated off. The aqueous phase is extracted twice with dichloromethane and the combined organic phases are dried over magnesium sulfate. The title compound is obtained as a yellow resin after evaporation of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117873
Source datasetuspto-grants-2000_09
ORD IDord-bc2cd44919154f3abf6da06e70be51a8
Source noteuspto-grants-2000_09