Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993269Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 22145797, compound

https://huagongshe.com/reaction/993269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22145873HCID 22145873—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 22145797HCID 2214579728.7%

Reaction Steps

Oxalyl chloride (50 mL) in dry dichloromethane (1.5 mL) is cooled to −30° C. under a nitrogen atmosphere. Dimethyl sulphoxide (80 mL) is added, the mixture stirred for 10 minutes then a solution of (±)-1-(4-cyclopentyloxy-5-methoxypyridin-2-yl)-2-(3,5-dichloropyridin-4-yl)ethanol (210 mg) in dichloromethane (2.5 mL) is added and the mixture stirred for 3 hours. Triethylamine (0.2 mL) is added and the mixture is allowed to warm to room temperature. After pouring into water the organic phase is extracted into dichloromethane, the extracts washed sequentially with 1% aqueous sulphuric acid, water, saturated aqueous sodium bicarbonate and water. The extracts are dried (MgSO4) and evaporated to give a solid. The solid is triturated with pentane, collected and dried to give 1-(4-cyclopentyloxy-5-methoxypyridin-2-yl)-2-(3,5-dichloropyridin-4-yl)ethanone (60 mg), as an off-white solid, m.p. 132° C. [Elemental analysis: C, 56.80; H, 4.92; N, 7.10% calculated: C, 56.71; H, 4.78; N, 7.35%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472412B1
Source datasetuspto-grants-2002_10
ORD IDord-16b29e4deeaf4064878551e8c6a341aa
Source noteuspto-grants-2002_10