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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1081731Erstellt: 27. Oktober 2026

Acetonitrile → 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081731

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktBenzenesulfonyl chlorideHCID 7369—
EduktTriethylamineHCID 8471—
Edukt5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochlorideHCID 23362997—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridineHCID 2336297859,5%

Reaktionsschritte

To a suspension of 5-[3-(amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride (2.64 g, 10 mmoles) and triethylamine (4.88 ml, 35 mmoles) in methylene chloride (100 ml)-acetonitrile (30 ml) was added benzenesulfonyl chloride (1.53 ml, 12 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the crude product thus obtained was recrystallized from methylene-ethanol to obtain 1.97 g of the desired product (59.5%, light brown crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05587383
Quelldatensatzuspto-grants-1996_12
ORD IDord-c56ed5989ed84cc5bfbbb44632686694
Quellennotizuspto-grants-1996_12