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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608615Generated: October 26, 2026

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

https://huagongshe.com/reaction/1608615

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 1 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 numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-962cd643795f45739b968272f8031915
Source noteuspto-grants-1995_03