반응 #1787796

ord-0339d7586cff4b1ea550047c02006054

용매

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The reaction solution was concentrated under reduced pressure
  2. 2
    workup.ADDITIONto the residue were added ethyl acetate (30 ml), tetrahydrofuran (20 ml) and 0.2 N sodium hydroxide (15 ml)
  3. 3
    workup.STIRRINGThe mixture was shaken
  4. 4
    세척the separated upper layer was washed with 0.2 N sodium hydroxide (10 ml) and water (10 ml, thrice)
  5. 5
    workup.ADDITIONTo the upper layer was added 2 N hydrochloric acid (0.5 ml)
  6. 6
    농축the mixture was concentrated under reduced pressure
  7. 7
    세척The residue was washed with a mixture of ether (3 ml) and ethanol (1.5 ml)
  8. 8
    기타dried

실험 절차

A mixture of 7-(2,6-dichlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one (153 mg), 1-amino-3-hydroxyguanidine p-toluenesulfonate (262 mg) and concentrated hydrochloric acid (0.1 ml) in ethanol (3 ml) was stirred at 90° C. (bath temperature) for 1.5 hours. The reaction solution was concentrated under reduced pressure, and to the residue were added ethyl acetate (30 ml), tetrahydrofuran (20 ml) and 0.2 N sodium hydroxide (15 ml). The mixture was shaken, and the separated upper layer was washed with 0.2 N sodium hydroxide (10 ml) and water (10 ml, thrice). To the upper layer was added 2 N hydrochloric acid (0.5 ml), and the mixture was concentrated under reduced pressure. The residue was washed with a mixture of ether (3 ml) and ethanol (1.5 ml) and dried to give 7-(2,6-dichlorophenyl)-5-(1-hydroxyguanidin-3-yl)imino-4-methyl-5,6,7,8-tetrahydroquinoline hydrochloride (Compound 96) as pale yellow crystals.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06350749B1uspto-grants-2002_02