Réaction #54200

ord-16bc665813b143e29c93a98dc8764fd4

Équation de réaction

CS(=O)(=O)Nc1ccc(NS(C)(=O)=O)c(S)c1
2-mercapto-N,N'-p-phenylenebismethanesulfonamide
ClCCN1CCCCC1
2-(1-piperidinyl)ethyl chloride
CS(=O)(=O)Nc1ccc(NS(C)(=O)=O)c(SCCN2CCCCC2)c1.Cl
title compound
CS(=O)(=O)Nc1ccc(NS(C)(=O)=O)c(SCCN2CCCCC2)c1.Cl
2-(2-(1-Piperidinyl)ethylthio)-N,N'-p-phenylenebismethanesulfonamide Hydrochloride

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction flask was then removed from the heat
  2. 2
    AutreAt the end of a period of 15 hours the precipitated white solid product (8.9 g) was collected on
  3. 3
    Filtrationa filter
  4. 4
    Autredried
  5. 5
    AutreRecrystallization
  6. 6
    workup.ADDITIONfrom a mixture of nitromethane and dimethylformamide

Mode opératoire

To a solution containing 8.9 g (0.030 mole) of 2-mercapto-N,N'-p-phenylenebismethanesulfonamide dissolved in 500 ml of ethanol at 60° C. was added 4.7 g (0.032 mole) of 2-(1-piperidinyl)ethyl chloride with stirring. The reaction flask was then removed from the heat, and the mixture was allowed to cool to room temperature. At the end of a period of 15 hours the precipitated white solid product (8.9 g) was collected on a filter and dried. Recrystallization from a mixture of nitromethane and dimethylformamide gave the title compound as white crystals, m.p. 218°-218.5° C. dec.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04147723uspto-grants-1979_04