Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677056Generated: November 1, 2026

Pyridine → HCID 67374254, compound

https://huagongshe.com/reaction/1677056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67374557HCID 67374557—
SolventWaterHCID 962—
ProductHCID 67374254HCID 67374254—

Reaction Steps

Under ice-cooling, oxalyl chloride (0.27 mL) was added dropwise into a dichloromethane (5 mL) solution containing 1-[(3S,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanol (269 mg) and pyridine (5 mL). Stirring was continued for 30 minutes at the same temperature and for 1 hour at room temperature. Water was added, and the organic layer was partitioned, and the resultant was dried over anhydrous magnesium sulfate. The solvent was removed under a vacuum, and the resultant was purified by silica gel column chromatography (heptane/ethyl acetate→ethyl acetate), and the title compound (136 mg) was obtained. The physical property values are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008293B2
Source datasetuspto-grants-2011_08
ORD IDord-67debe9f2b4f4e35bff7c36e03d49cd8
Source noteuspto-grants-2011_08