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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727378Generated: November 1, 2026

Dimethyl Sulfoxide → N-{4-[2-Acetyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]pyridin-2-yl}propanamide

https://huagongshe.com/reaction/1727378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantN-{4-[2-(1-Hydroxyethyl)-4-(3-methylphenyl)-1,3-thiazol-5-yl]pyridin-2-yl}propanamideHCID 53432117—
SolventDichloromethaneHCID 6344—
ProductN-{4-[2-Acetyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]pyridin-2-yl}propanamideHCID 5343212160.2%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A solution of dimethylsulfoxide (0.30 mL, 4.2 mmol) in dichloromethane (1.0 mL) was added to a solution of oxalyl chloride (0.11 mL, 1.26 mmol) at −78° C. and the resulting mixture was stirred for 15 minutes. A solution of N-[4-[2-(1-hydroxyethyl)-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]propionamide (0.38 g, 1.0 mmol) in dichloromethane (1.5 mL) was added to the mixture and the resulting mixture was stirred for 45 minutes. The reaction mixture was allowed to warm up to −50° C. and triethylamine (0.72 mL, 5.17 mmol) was added dropwise to the mixture. The resulting mixture was stirred for 30 minutes and poured into aqueous sodium hydrogen carbonate. The mixture was extracted with ethyl acetate and the extracts were washed with aqueous sodium hydrogen carbonate solution and brine. The resulting solution was dried, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate=2:1) to obtain a crude crystal. The obtained crude crystal was recrystallized from isopropyl ether to give a title compound (0.22 g, yield 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495018B2
Source datasetuspto-grants-2009_02
ORD IDord-e37c7190c9db48e1a23c2bc1c38db959
Source noteuspto-grants-2009_02