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HRID 1953774Erstellt: 26. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSilane, bromotriethyl-HCID 70680—
Eduktdimethyl N-(7-nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-alpha-(ethylamino)ethylphosphonateHCID 23298022—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2,3-Dioxo-7-nitro-1,2,3,4-tetrahydroquinoxalin-5-ylmethyl)-alpha-(ethylamino)ethylphosphonic acid hydrobromideHCID 17967587—

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06117873
Quelldatensatzuspto-grants-2000_09
ORD IDord-805450e2d57f40898fcf73124a490141
Quellennotizuspto-grants-2000_09