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

HRID 2286337Notes

Reaction equation

HRID 2286337 reaction equation
[Cl:1][C:2]1[C:3]([CH2:8][S:9][CH2:10][CH2:11][NH2:12])=[N:4][CH:5]=[CH:6][CH:7]=1.CS[C:15](=[N:20][CH3:21])[S:16]([O-:19])(=[O:18])=[O:17]>C(#N)C>[Cl:1][C:2]1[C:3]([CH2:8][S:9][CH2:10][CH2:11][NH:12][C:15]([S:16]([OH:19])(=[O:17])=[O:18])=[N:20][CH2:21][CH2:10][S:9][CH2:8][C:3]2[C:2]([Cl:1])=[CH:7][CH:6]=[CH:5][N:4]=2)=[N:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 129515322-(3-Chloropyrid-2-ylmethylthio)ethylamineHCID 867370781-Methylthio-1-methyliminomethanesulphonate

Product 1

HCID 53709668N,N'-bis-[2-(3-chloropyrid-2-ylmethylthio)ethyl]amidinosulphonic acid

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent2×

Procedure

A solution of 2-(3-chloropyrid-2-ylmethylthio)ethylamine (4.06 g) in dry acetonitrile (200 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 1 hour and then allowed to cool. The mixture was evaporated 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 microanalysis and nuclear magnetic resonance spectroscopy to the title compound.

Workup

  1. temperatureto cool
  2. customThe mixture was evaporated to dryness
  3. dissolutiondissolved in methanol
  4. customabsorbed onto silica gel
  5. customChromatography on a column of silica gel produced a viscous oil which
  6. customwas collected
  7. washby eluting the column with a chloroform/methanol mixture
  8. customevaporating off the solvent

Sources & evidence

ORD record
ord-3a1c40ac682643caa6a482aa0893cdbb
Source dataset
uspto-grants-1981_05
Patent number
US04265896

Reaction notes

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