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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057372Generated: October 26, 2026

2-(3-Chloropyrid-2-ylmethylthio)ethylamine → N-Methyl-N'-[2-(3-chloropyrid-2-ylmethylthio)ethyl]-amidinosulphonic acid

https://huagongshe.com/reaction/2057372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Chloropyrid-2-ylmethylthio)ethylamineHCID 12951532—
Reactant1-Methylthio-1-methyliminomethanesulphonateHCID 86737078—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductN-Methyl-N'-[2-(3-chloropyrid-2-ylmethylthio)ethyl]-amidinosulphonic acidHCID 178484988—

Reaction Steps

A solution of 2-(3-chloropyrid-2-ylmethylthio)ethylamine (2.03 g) in dry acetonitrile (150 ml) was added dropwise, with stirring, to a solution of 1-methylthio-1-methyliminomethanesulphonate (1.69 g) in dry acetonitrile (150 ml) at 50°. The mixture was stirred at 60° for 30 minutes and then allowed to cool. The mixture was stripped to dryness, dissolved in methanol and absorbed onto silica gel. Chromatography on a column of silica gel produced a viscous oil which was collected by eluting the column with a chloroform/methanol mixture and evaporating off the solvent. The viscous oil analysed by micro-analysis and nuclear magnetic resonance spectroscopy to the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04210658
Source datasetuspto-grants-1980_07
ORD IDord-e6c21e35e56d4437b6e99ce321c38cc3
Source noteuspto-grants-1980_07