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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031965Generated: October 30, 2026

Ethanol → N-(6-Methanesulphonamido-2-quinolylmethyl)-N-methyl-4-methanesulphonamidophenethylamine

https://huagongshe.com/reaction/1031965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Chloromethyl-6-methanesulphonamidoquinolineHCID 19045572—
ProductN-(6-Methanesulphonamido-2-quinolylmethyl)-N-methyl-4-methanesulphonamidophenethylamineHCID 19813423—

Reaction Steps

4-[2-(Methylamino)ethyl]methanesulphonanilide (0.228 g, 1 mmol--see Preparation 14(B)) and 2-chloromethyl-6-methanesulphonamidoquinoline (0.135 g, 0.5 mmol--see Preparation 12(D)) were heated in ethanol solution (5 ml) at reflux for 4 hours. The solvent was then evaporated in vacuo and the residue dissolved in methylene chloride, washed with water, dried (MgSO4), filtered and evaporated in vacuo. The resulting gum was purified by column chromatography on silica eluting with methylene chloride containing methanol (0% up to 1%). The product-containing fractions were combined and evaporated in vacuo to give a foam which crystallised from ethanol, yield of the title compound 0.45 g, m.p. 165°-166°, confirmed spectroscopically to be identical to the product of Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956382
Source datasetuspto-grants-1990_09
ORD IDord-f6e2e1a2fd424c3ba325b18ff7fb0eef
Source noteuspto-grants-1990_09