Reacción #51740

ord-6a1054619fbc4fcb904c96e147584521

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe organic layer was washed with 2N HCl, H2O, saturated sodium bicarbonate solution and brine
  2. 2
    Secadowas dried (MgSO4)
  3. 3
    OtroThe solvents were evaporated
  4. 4
    Otrothe residue was purified by flash chromatography (100% hexanes to 25% EtOAc in hexanes)

Procedimiento

To 4-isopropyl-7-methyl-6-thiocyanato-benzothiazol-2-yl-amine (Example L-4; 4.0 g, 17 mmol) dissolved in CH2Cl2 (25 mL) and pyridine (5 mL), was added methyl chloroformate at 0° C. The reaction mixture was stirred at room temperature for 2 hours. H2O was added to the reaction mixture followed by EtOAc (100 mL). The organic layer was washed with 2N HCl, H2O, saturated sodium bicarbonate solution and brine, and was dried (MgSO4). The solvents were evaporated, and the residue was purified by flash chromatography (100% hexanes to 25% EtOAc in hexanes) to give 2-(methyloxycarbonyl)amino-4-isopropyl-7-methyl-6-thiocyanato-benzothiazole. MS (APCI): 322 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06852711B2uspto-grants-2005_02