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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4297Erstellt: 25. Oktober 2026

Dimethylamine → 8-(2-Chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/4297

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktFormaldehydeHCID 712—
Edukt8-(2-Chlorobenzyloxy)-2-methylimidazo[1,2-a]pyridineHCID 13825932—
LösungsmittelAcetic AcidHCID 176—
Produkt8-(2-Chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridineHCID 1382593685,4%

Reaktionsschritte

To a solution of 37% aqueous formaldehyde (2.38 g) in acetic acid (38 ml) was added dropwise 50% aqueous dimethylamine (2.63 g) with ice-cooling over a period of 10 minutes and the mixture was stirred for an additional 10 minutes. The mixture was heated at 50°-55° C. for 2 hours after an addition of 8-(2-chlorobenzyloxy)-2-methylimidazo[1,2-a]pyridine (7.6 g) thereto and then evaporated in vacuo. The residue was basified with aqueous sodium hydroxide and extracted with methylene chloride. The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residual solid was recrystallized from a mixture of diethyl ether and n-hexane to give 8-(2-chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridine (7.85 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725601
Quelldatensatzuspto-grants-1988_02
ORD IDord-92e60f8984b44a1db9d8ae0442b210af
Quellennotizuspto-grants-1988_02