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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295020Generated: November 1, 2026

Methanesulfonyl chloride → HCID 54334405, compound

https://huagongshe.com/reaction/2295020

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 numberUS05691366
Source datasetuspto-grants-1997_11
ORD IDord-16233c20b2e748d89d2ea434b612fb7c
Source noteuspto-grants-1997_11