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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953774Generated: October 25, 2026

Silane, bromotriethyl- → N-(2,3-Dioxo-7-nitro-1,2,3,4-tetrahydroquinoxalin-5-ylmethyl)-alpha-(ethylamino)ethylphosphonic acid hydrobromide

https://huagongshe.com/reaction/1953774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilane, bromotriethyl-HCID 70680—
Reactantdimethyl N-(7-nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-(ethylamino)ethylphosphonateHCID 23298022—
SolventDichloromethaneHCID 6344—
ProductN-(2,3-Dioxo-7-nitro-1,2,3,4-tetrahydroquinoxalin-5-ylmethyl)-alpha-(ethylamino)ethylphosphonic acid hydrobromideHCID 17967587—

Reaction Steps

160 mg (0.37 mmol) of dimethyl N-(7-nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-α-(ethylamino)ethylphosphonate are dissolved in 8 ml of dichloromethane and stirred at room temperature for one hour with 0.19 ml (4 eq.) of triethylbromosilane. The solvent and excess reagent are evaporated and the residue is briefly dried in a high vacuum, dissolved in 5 ml of an about 33% hydrogen bromide solution in acetic acid, and stirred at room temperature for 18 hours. The reaction mixture is diluted with diethyl ether, and the solid is filtered off, washed with diethyl ether and dried. The title compound is obtained as a beige solid; m.p.=191° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117873
Source datasetuspto-grants-2000_09
ORD IDord-805450e2d57f40898fcf73124a490141
Source noteuspto-grants-2000_09