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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396916Generated: October 29, 2026

Methanesulfonyl chloride → HCID 54334405, compound

https://huagongshe.com/reaction/2396916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 54352395HCID 54352395—
SolventPyridineHCID 1049—
ProductHCID 54334405HCID 54334405—

Reaction Steps

A solution of N-(4-ethyl-2,4-hexadien-1-yl)-6-amino-3-pyridinecarboxamide (3.0 g) and methanesulfonyl chloride (1.54 g) in pyridine (25 ml) was stirred at 50° C. for 3 hours. The reaction mixture was evaporated in vacuo and the residue was dissolved in ethyl acetate. The solution was washed with 0.5N hydrochloric acid and brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (3% methanol-chloroform) to give N-(4-ethyl-2,4-hexadien-1-yl)-6-methansulfonamido-3-pyridinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05495023
Source datasetuspto-grants-1996_02
ORD IDord-07bcfa5d29fc4b1f88b1e0a63ae5badd
Source noteuspto-grants-1996_02