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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1430792Erstellt: 25. Oktober 2026

Benzenemethanamine, N-ethyl-4-methoxy- → 7-bromo-2-chloro-N-ethyl-N-(4-methoxybenzyl)imidazo[2,1-f][1,2,4]triazin-4-amine

https://huagongshe.com/reaction/1430792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenemethanamine, N-ethyl-4-methoxy-HCID 296018—
Edukt7-Bromo-2,4-dichloroimidazo[2,1-f][1,2,4]triazineHCID 86708472—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-bromo-2-chloro-N-ethyl-N-(4-methoxybenzyl)imidazo[2,1-f][1,2,4]triazin-4-amineHCID 86708471106,8%

Reaktionsschritte

(I10A): A solution of 7-bromo-2,4-dichloroimidazo[2,1-f][1,2,4]triazine (Intermediate I9F) (10 g, 37.3 mmol) in anhydrous THF (300 ml) was treated with N-(4-methoxybenzyl)ethanamine (8.01 ml, 46.7 mmol), resulting in the immediate precipitation of a solid. The reaction was stirred for 1 hour; the mixture was concentrated in vacuo. To the residue was added EtOAc (100 ml) and the mixture stirred 10 min. The salts were filtered off and the filtrate was washed with 0.5M citric acid, sat. NaHCO3, water and brine. The solution was dried over Na2SO4 and solvents removed to afford 7-bromo-2-chloro-N-ethyl-N-(4-methoxybenzyl)imidazo[2,1-f][1,2,4]triazin-4-amine (15.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08940736B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-19ce917159a64f9090aa927e58eba1c3
Quellennotizuspto-grants-2015_01