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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914668Generated: November 2, 2026

Pyridine → HCID 178432776, compound

https://huagongshe.com/reaction/1914668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178432775HCID 178432775—
SolventDichloromethaneHCID 6344—
ProductHCID 178432776HCID 178432776—

Reaction Steps

A solution of Trans-5-chloro-N-(4-hydroxymethyl-cyclohexyl)-2-methyl-nicotinamide (step 1) (100 mg, 0.354 mmol) and pyridine (3.6 ml) in dry DCM (3.5 ml) under nitrogen is cooled to approx. 0° C. using an ice-water bath. Methanesulfonyl chloride (0.030 ml, 0.389 mmol) is added dropwise. The reaction mixture is allowed to warm to room temp and stirred at this temp for 4 hours. The reaction is quenched by the addition of sat. NH4Cl at room temp and then extracted with diethyl ether (3×20 ml). The Et2O extracts are combined, washed with sat brine (20 mL), dried (MgSO4), filtered and evaporated to give the title compound as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614213B2
Source datasetuspto-grants-2013_12
ORD IDord-be95e368f3df4c46ae8f8c3e7d73279f
Source noteuspto-grants-2013_12