反应 #2358564

ord-145b19df304a427094b3575e194e6e8e

反应方程式

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
收率 75.0%

反应条件

温度
62.5°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度maintained for 60 minutes
  2. 2
    过滤The product was filtered under nitrogen
  3. 3
    洗涤washed with chilled acetonitrile
  4. 4
    workup.STIRRINGstirred for 30 min
  5. 5
    温度The reaction mixture was gradually cooled to 25° C.
  6. 6
    workup.STIRRINGstirred for 1 hour
  7. 7
    过滤The product was filtered under vacuum and nitrogen atmosphere
  8. 8
    洗涤The wet-cake was washed with chilled acetonitrile
  9. 9
    其他The product was dried under vacuum at 50-55° C.

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09120755B2uspto-grants-2015_09