Réaction #1003499

ord-142e262cbb384408977646cb6917763c

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added
  2. 2
    AutreThe tube was capped
  3. 3
    Autrethe reaction tube was exposed to microwave irradiation (100° C., 3 min)
  4. 4
    AutreThe pyrrolidine was evaporated
  5. 5
    Autrethe reaction mixture was transferred to a separation funnel with ethyl acetate
  6. 6
    Lavagewashed with 2 M NaOH
  7. 7
    Extractionextracted with ethyl acetate
  8. 8
    AutreThe organic phases were collected
  9. 9
    Séchagedried over Na2SO4
  10. 10
    Filtrationfiltered
  11. 11
    Concentrationconcentrated

Mode opératoire

154BG85-11 (156 mg, 0.7 mmol) was transferred to a Pyrex tube and pyrrolidine (1 mL) was added. The tube was capped and the reaction tube was exposed to microwave irradiation (100° C., 3 min). The microwave exposure was repeated for 5 min at 130° C. The pyrrolidine was evaporated and the reaction mixture was transferred to a separation funnel with ethyl acetate and washed with 2 M NaOH. The aqueous phase was acidified with 2 M HCl and extracted with ethyl acetate. The organic phases were collected, dried over Na2SO4, filtered and concentrated to yield 135 mg (70%) of the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07268232B2uspto-grants-2007_09