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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761873Generated: October 28, 2026

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

https://huagongshe.com/reaction/1761873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indaneHCID 15023223—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
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 evaporation 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 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 numberUS04829071
Source datasetuspto-grants-1989_05
ORD IDord-9652492b00294be1a172c2e304feac5b
Source noteuspto-grants-1989_05