Reacción #9256

ord-955b7113daa34b80b77e74e52f6c7686

Disolventes

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe toluene was removed in vacuo
  2. 2
    LavadoThe organic phase was washed with 0.5 M NaOH (2 times)
  3. 3
    Secadodried over MgSO4
  4. 4
    OtroThe crude oil was purified by flash chromatography on SiO2 (EtOAc/CH2Cl2 5/95)
  5. 5
    Otro445 mg (85%, 2 steps) of pure product was isolated

Procedimiento

To a mixture of N-ethyl-N′-[7-(phenylsulfanyl)-4,5-dihydro-1,3-benzothiazol-2-yl]urea (crude product from the previous reaction, 1.59 mmol) in toluene (35.0 mL) was added DDQ (500 mg, 2.17 mmol). The reaction mixture was stirred at about 20° C. for about 2 hrs. The toluene was removed in vacuo and the crude material was taken up in CH2Cl2. The organic phase was washed with 0.5 M NaOH (2 times) and dried over MgSO4. The crude oil was purified by flash chromatography on SiO2 (EtOAc/CH2Cl2 5/95). 445 mg (85%, 2 steps) of pure product was isolated. LC/MS 330 (MH+); RP-HPLC RT 17.56 min.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091227B2uspto-grants-2006_08