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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081731Generated: October 26, 2026

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

https://huagongshe.com/reaction/1081731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochlorideHCID 23362997—
SolventDichloromethaneHCID 6344—
Product5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridineHCID 2336297859.5%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-c56ed5989ed84cc5bfbbb44632686694
Source noteuspto-grants-1996_12