Reaktion #8718

ord-6f110095d41b437f9aec3433c29d3d1d

Reaktionsgleichung

CCOc1ccccc1-c1nc2c(C3CCCC3)nc(C)n2c(=O)[nH]1
8-cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one
CCOc1ccccc1-c1nc2c(C3CCCC3)nc(C)n2c(=O)[nH]1
8-Cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one
O=S(=O)(O)Cl
chlorosulfonic acid
CCOc1ccc(S(=O)(=O)Cl)cc1-c1nc2c(C3CCCC3)nc(C)n2c(=O)[nH]1
4-Ethoxy-3-(8-cyclopentyl-6-methyl-4-oxo-3,4-dihydro-imidazol[1,5-a][1,3,5]-triazin-2-yl)-benzenesulfonyl chloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONpoured onto ice water
  2. 2
    SonstigeThe organic phase is separated off
  3. 3
    ExtraktionThe aqueous phase is extracted once again with dichloromethane
  4. 4
    Sonstigedried
  5. 5
    Sonstigeevaporated

Vorschrift

372.3 mg (1.1 mmol) of 8-cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one (example IX) are added in portions to 0.66 ml (9.9 mmol) of ice-cooled chlorosulfonic acid. The mixture is subsequently stirred overnight at room temperature before being diluted with dichloromethane and poured onto ice water. The organic phase is separated off. The aqueous phase is extracted once again with dichloromethane and the organic phases are combined, dried and evaporated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091203B2uspto-grants-2006_08