Reacción #925

ord-a5a19d2e3ccc4cb7bff13f06f043ffc0

Ecuación de reacción

Cl
HCl
COC(=O)c1ccn(C)c1S(N)(=O)=O
Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylate
COc1nc(C)nc(NC(=O)Oc2ccccc2)n1
phenyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate
C1CCC2=NCCCN2CC1
DBU
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)NC1=NC(OC)=CN(C)N1
oil
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)NC1=NC(OC)=CN(C)N1
Methyl 2-[[[[(4-Methoxy-6-methyl-1,3,6-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrrole-3-carboxylate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe resulting precipitate was collected by filtration
  2. 2
    Lavadorinsed successively with water and ether
  3. 3
    Otrodried

Procedimiento

Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylate (0.10 g, 0.46 mmol) and 0.13 g (0.50 mmol) of phenyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate were combined in 2 mL of acetonitrile and 0.075 mL of DBU was added and the resulting amber solution was stirred at ambient temperature for 30 min. The reaction mixture was diluted with 15 mL of water and acidified with 0.5 mL 1N HCl and the resulting precipitate was collected by filtration and rinsed successively with water and ether, then dried to afford 0.13 g oil the title compound as a white solid, m.p. 189°-190° C. (dec).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723410uspto-grants-1998_03