반응 #1947

ord-dbb3e314646f42c4828e49ee8c678c63

용매

반응 조건

온도
65°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the stirred reaction mixture
  2. 2
    온도to cool to ambient temperature
  3. 3
    농축concentrated in vacuo in order
  4. 4
    기타to remove all of the pyridine
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in 60 mL of methylene chloride
  6. 6
    세척the methylene chloride solution was washed with 60 mL of water
  7. 7
    추출The aqueous layer was extracted with 2 X 60 mL of methylene chloride
  8. 8
    건조the combined methylene chloride solutions were dried over anhydrous sodium sulfate
  9. 9
    여과filtered
  10. 10
    농축concentrated
  11. 11
    기타dried in vacuo

실험 절차

Ethyl 8-chloro-1-ethyl-4H-quinolizin-4-one-3-carboxylate (558 mg, 2.0 mmol), the product of Step 3 of Example 62, was dissolved in 10 mL of dry pyridine under a nitrogen atmosphere. To the resultant solution was added 600 mg (6.0 mmol) of 2-methylpiperazine and the stirred reaction mixture was heated at 65° C. for 3 hours. The reaction mixture was allowed to cool to ambient temperature and then concentrated in vacuo in order to remove all of the pyridine. The residue was dissolved in 60 mL of methylene chloride and the methylene chloride solution was washed with 60 mL of water. The aqueous layer was extracted with 2 X 60 mL of methylene chloride and the combined methylene chloride solutions were dried over anhydrous sodium sulfate, filtered and concentrated and dried in vacuo to afford 690 mg of the title compound. The product was carried on to the next step without purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726182uspto-grants-1998_03