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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824515Generated: October 25, 2026

Triethylamine → 2-[4-[4-Methanesulfonyloxybutyl]phenyl]-7-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1824515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-[4-[4-Hydroxybutyl]phenyl]-7-methylimidazo[1,2-a]pyridineHCID 22015655—
SolventDichloromethaneHCID 6344—
Product2-[4-[4-Methanesulfonyloxybutyl]phenyl]-7-methylimidazo[1,2-a]pyridineHCID 22015658125.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

The product of Step A (0.33 g) in dichloromethane (20 mL) was treated with triethylamine (0.36 g) and cooled to 0° C. The cold solution was treated with methanesulfonyl chloride (0.338 g) and allowed to stir and warm to ambient temperature over 18 hours. The reaction mixture was washed with water (50 mL), saturated sodium bicarbonate solution (25 mL), water (50 mL), dried over sodium sulfate, filtered and evaporated to give the crude title compound (0.53 g). The crude product was used, Step C, without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041827B2
Source datasetuspto-grants-2006_05
ORD IDord-3298874fa03e4337a906ddb4a2232ba9
Source noteuspto-grants-2006_05