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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084901Generated: October 31, 2026

Methanesulfonyl chloride → 2-[N-(4-Methanesulphonamidobenzyl)-N-methylamino]-5-methanesulphonamidoindane

https://huagongshe.com/reaction/1084901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indaneHCID 15023223—
SolventPyridineHCID 1049—
Product2-[N-(4-Methanesulphonamidobenzyl)-N-methylamino]-5-methanesulphonamidoindaneHCID 15014992—

Reaction Steps

Methanesulphonyl chloride (0.53 ml) was added to 5-amino-2-[N-(4-aminobenzyl)-N-methylamino]indane (1.1 g) in pyridine and the reaction mixture was stirred at room temperature for 17 hours. The solvent was then removed by evaportion in vacuo and the residue taken up in methylene chloride, washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo. The resulting gum was purified by column chromatography on silica eluting with methylene chloride containing methanol (0% up to 2%). The product-containing fractions were combined and evaporated to dryness in vacuo to give the title compound as a colourless foam. This foam was dissolved in chloroform and the solution was evaporated to dryness in vacuo to give the title compound as a colourless foam, yield 0.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006561
Source datasetuspto-grants-1991_04
ORD IDord-7cfae9147c274e2294095c92f2aa80b3
Source noteuspto-grants-1991_04