Réaction #2358564

ord-145b19df304a427094b3575e194e6e8e

Équation de réaction

COc1cc2c(cc1OC)CC(=O)N(CCCN(C)C[C@H]1Cc3cc(OC)c(OC)cc31)CC2
ivabradine
CC#N.Cl
acetonitrile hydrochloric acid
COc1cc2c(cc1OC)CC(=O)N(CCCN(C)C[C@H]1Cc3cc(OC)c(OC)cc31)CC2.Cl
ivabradine hydrochloride
Rendement 75.0%

Solvants

Conditions de réaction

Température
62.5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températuremaintained for 60 minutes
  2. 2
    FiltrationThe product was filtered under nitrogen
  3. 3
    Lavagewashed with chilled acetonitrile
  4. 4
    workup.STIRRINGstirred for 30 min
  5. 5
    TempératureThe reaction mixture was gradually cooled to 25° C.
  6. 6
    workup.STIRRINGstirred for 1 hour
  7. 7
    FiltrationThe product was filtered under vacuum and nitrogen atmosphere
  8. 8
    LavageThe wet-cake was washed with chilled acetonitrile
  9. 9
    AutreThe product was dried under vacuum at 50-55° C.

Mode opératoire

100 g of ivabradine base and 300 mL acetonitrile were cooled to 0° C. to 5° C. and acetonitrile hydrochloric acid solution was added drop wise by adjusting the pH to about 1-2. The resulting mass was stirred till complete precipitation and maintained for 60 minutes. The product was filtered under nitrogen and washed with chilled acetonitrile. The wet-cake and acetonitrile were heated at 60-65° C. and stirred for 30 min. The reaction mixture was gradually cooled to 25° C. and stirred for 1 hour. The product was filtered under vacuum and nitrogen atmosphere. The wet-cake was washed with chilled acetonitrile. The product was dried under vacuum at 50-55° C. to obtain 75% 80 g crude ivabradine hydrochloride. The product was packed in double polyethene bag under nitrogen.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09120755B2uspto-grants-2015_09