Reacción #69152

ord-bec13ed6940f480b9c2f51608e0d42b8

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONcompletely dissolved
  2. 2
    Otroto remove organic solvents
  3. 3
    FiltraciónThe resulting solution was then filtered through a 0.65 μm cartridge
  4. 4
    workup.ADDITIONdiluted with water (2.1 liter)
  5. 5
    Lavadoto rinse the reactor and pipelines
  6. 6
    TemperaturaThe solution was cooled down to 50° C.
  7. 7
    workup.ADDITION7 g of Nalmefene hydrochloride dihydrate seeding material was added
  8. 8
    TemperaturaThe mixture was cooled down to 0-5° C. in one hour
  9. 9
    Temperaturamaintained
  10. 10
    workup.STIRRINGunder stirring for one additional hour
  11. 11
    FiltraciónThe solid was filtered
  12. 12
    Lavadowashed with acetone
  13. 13
    OtroThe wet product was dried at 25° C. under vacuum

Procedimiento

Crude Nalmefene hydrochloride (7.67 Kg, assay 93.9%) and water (8.6 liter) were charged into a suitable reactor. The suspension was heated up to 80° C. until the substrate completely dissolved. Vacuum was then applied to remove organic solvents. The resulting solution was then filtered through a 0.65 μm cartridge and then diluted with water (2.1 liter) used to rinse the reactor and pipelines. The solution was cooled down to 50° C. and 7 g of Nalmefene hydrochloride dihydrate seeding material was added. The mixture was cooled down to 0-5° C. in one hour under efficient stirring and then maintained under stirring for one additional hour. The solid was filtered and washed with acetone. The wet product was dried at 25° C. under vacuum to provide Nalmefene hydrochloride dihydrate (5.4 Kg; yield 73%) with a chemical purity of 99.89% (HPLC).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08530495B2uspto-grants-2013_09