Reaktion #925

ord-a5a19d2e3ccc4cb7bff13f06f043ffc0

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe resulting precipitate was collected by filtration
  2. 2
    Waschenrinsed successively with water and ether
  3. 3
    Sonstigedried

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723410uspto-grants-1998_03