반응 #6211

ord-a551cb2a1c7144368de100ddce8580d5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooling
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature for 30 minutes
  3. 3
    세척The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water
  4. 4
    기타dried
  5. 5
    workup.DISTILLATIONthe solvent was distilled off
  6. 6
    기타The residue was purified by column chromatography (eluent: methanol/ethyl acetate=1:10)
  7. 7
    기타to obtain powder
  8. 8
    세척The powder was washed with ether
  9. 9
    기타dried

실험 절차

To a solution of 396 mg (1.64 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 0.27 ml (1.97 mmol) of triethylamine in 20 ml of methylene chloride, 500 mg (1.96 mmol) of 3-quinolineacryloyl chloride hydrochlride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: methanol/ethyl acetate=1:10) to obtain powder. The powder was washed with ether and dried to obtain the desired compound (480 mg, yield: 83.8%, pale yellow powder).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246948uspto-grants-1993_09