Reacción #76610

ord-38230e1caae94cd4895788b5ea884686

Condiciones de reacción

Temperatura
95°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe mixture was partitioned between 12 ml of water and 3×4 ml of dichloromethane
  2. 2
    SecadoThe combined organic portions were dried (magnesium sulphate)
  3. 3
    Filtraciónfiltered
  4. 4
    Otroevaporated
  5. 5
    OtroThe product was purified by column chromatography (20 g IST pre-packed column)
  6. 6
    Lavadoeluting with ethyl acetate
  7. 7
    workup.ADDITIONtreated with 0.15 ml of 4M hydrogen chloride in dioxan
  8. 8
    OtroThe solvent was evaporated
  9. 9
    Otroto leave a red gum which
  10. 10
    Otrowas recrystallised from acetone/ethyl acetate/diethyl ether

Procedimiento

To a mixture of 56 mg (0.45 mmol) of 2-fluorobenzaldehyde and 64 mg (50 mmol) of 4-chlorophenol in 2.5 ml of dimethylformamide was added 75 mg (0.54 mmol) of sodium hydrogen carbonate. The mixture was heated at 95° C. for 18 hours. To the mixture at ambient temperature was added 118 mg (0.36 mmol) of (8-fluoro-1-methyl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl ester followed by 25 mg (0.63 mmol) of sodium hydride (60% dispersion in mineral oil). The mixture was stirred for 2 hours. The mixture was partitioned between 12 ml of water and 3×4 ml of dichloromethane. The combined organic portions were dried (magnesium sulphate), filtered and evaporated. The product was purified by column chromatography (20 g IST pre-packed column) eluting with ethyl acetate and treated with 0.15 ml of 4M hydrogen chloride in dioxan. The solvent was evaporated to leave a red gum which was recrystallised from acetone/ethyl acetate/diethyl ether to give 17 mg of (E)-5-[2-(4-chlorophenoxy)styryl]-8-fluoro-2,3-dihydro-1-methyl-1H-1,4-benzodiazepine dihydrochloride as a red solid; MS: m/e 452 (M+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06703387B2uspto-grants-2004_03