Reacción #1502969

ord-12c681ee31a34fa283d467b9400ced7e

Ecuación de reacción

CC(C=O)CC(=O)c1ccc(Cl)cc1
2-(4-chlorophenacyl)propionaldehyde
Nc1ccc(S(N)(=O)=O)cc1
4-sulfamoylaniline
Cc1cc(-c2ccc(Cl)cc2)n(-c2ccc(S(N)(=O)=O)cc2)c1
title compound
Cc1cc(-c2ccc(Cl)cc2)n(-c2ccc(S(N)(=O)=O)cc2)c1
2-(4-Chlorophenyl)-4-methyl-1-(4-sulfamoylphenyl)pyrrole

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Following a procedure similar to that described in Example 64(iii), but using 2-(4-chlorophenacyl)propionaldehyde [prepared as described in step (ii) above] and 4-sulfamoylaniline as starting materials, the title compound was obtained as a pale brown powder (yield 35%), melting at 196-198° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05908858uspto-grants-1999_06