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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984443Generated: October 30, 2026

Ethylmorpholine → HCID 22558362, compound

https://huagongshe.com/reaction/984443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22558433HCID 22558433—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22558362HCID 22558362—

Reaction Steps

14 mg (0.12 mmol) of methanesulphonyl chloride were added to a solution of 40 mg (0.1 mmol) of N-[3-methoxy-4-(5-oxazolyl)phenyl-N′-[1,1-dimethyl-2-(4-piperidinyl)ethyl]oxalamide in 1 ml of dichloromethane followed by 17 mg (0.15 mmol) of N-ethylmorpholine and the mixture stirred at room temperature for 4 hours. The resulting solution was diluted with ethyl acetate, washed with 2M hydrochloric acid and saturated sodium bicarbonate solution, dried over magnesium sulphate, evaporated to dryness and the residue triturated with diethyl ether. There was obtained 23 mg of N-[2-[1-(methanesulfonyl)-4-piperidinyl]-1,1-dimethylethyl]-N′-(3-methoxy-4-(5-oxazolyl)phenyl]oxalamide as an off-white solid. MS m/e 479 [M+]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867299B2
Source datasetuspto-grants-2005_03
ORD IDord-1b275c0aa4df400f906ab55657739a66
Source noteuspto-grants-2005_03