Réaction #81685

ord-18fec9a30f8d426199d4e419529c510e

Équation de réaction

CCCN=C=O
n-propyl isocyanate
NS(=O)(=O)c1ccccc1I
2-iodo benzene sulfonamide
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(C)=O.CC(C)OC(C)C
acetone isopropyl ether
CCCS(=O)(=O)NC(N)=O.Ic1ccccc1
title compound
CCCS(=O)(=O)NC(N)=O.Ic1ccccc1
2-iodobenzene n-propylsulfonylurea

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe mixture is refluxed under N2 -atmosphere
  2. 2
    TempératureAfter 2 hours reflux
  3. 3
    Concentrationconcentrated to dryness
  4. 4
    workup.ADDITIONWater (200 ml) is added
  5. 5
    Filtrationfiltered
  6. 6
    AutreThe precipitate obtained

Mode opératoire

To a stirred solution of 2-iodo benzene sulfonamide (4 g) in acetone (40 mi) solid K2CO3 (3.92 g) is added in one portion and the mixture is refluxed under N2 -atmosphere, n-propyl isocyanate is added dropwise to the heated mixture. After 2 hours reflux, the reaction is cooled to room temperature and concentrated to dryness. Water (200 ml) is added and the cooled mixture is acidified with 2N HCl to pH 4 and filtered. The precipitate obtained is recristallised with acetone/isopropyl ether mixture to give 4.1 g solid of the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05618975uspto-grants-1997_04