Reaktion #1280636

ord-515d729af01a4916b94c28052f22c858

Reaktionsgleichung

[CH3][Al]([CH3])[CH3]
trimethylaluminum
Cn1cc(-c2ccccc2S(N)(=O)=O)cn1
2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide
COC(=O)Nc1nc(C)nc(OC)n1
methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-c2cnn(C)c2)n1
title compound
Ausbeute 17.6%
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-c2cnn(C)c2)n1
N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide
Ausbeute 17.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter work up and evaporation of the methylene chloride solvent
  2. 2
    Sonstigethe residue was triturated with ethyl acetate

Vorschrift

By the procedure of Example 14, 2 g of 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide, prepared in Example 19, was reacted in 100 ml of methylene chloride with 0.7 g of trimethylaluminum (5 ml of 2M toluene solution) followed by 1.7 g of methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate. After work up and evaporation of the methylene chloride solvent, the residue was triturated with ethyl acetate to yield 0.6 g of the title compound; m.p. 221°-224° C. The IR spectrum showed a carbonyl absorption at 1700 cm-1 indicative for a sulfonylurea.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04810282uspto-grants-1989_03