반응 #78163

ord-2d57d14ff339450ebd4864938eadbeb0

반응 조건

온도
200°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도is heated
  2. 2
    기타has formed
  3. 3
    workup.STIRRINGthe reaction mixture stirred for a further 3.5 h at 205° C
  4. 4
    온도After cooling to about 170° C.
  5. 5
    workup.STIRRINGThe mixture is stirred for a further 30 min
  6. 6
    온도while cooling to RT
  7. 7
    건조The organic phase dried over sodium sulfate
  8. 8
    농축is concentrated by evaporation
  9. 9
    기타the residue purified on silica gel by flash chromatography

실험 절차

A mixture of 2.39 g (16.8 mmol) phosphorus pentoxide, 2.31 g (16.8 mmol) triethylamine hydrochloride, and 1.82 ml (16.8 mmol) m-toluidine is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 1 g (4.2 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3.5 h at 205° C. After cooling to about 170° C., 4 ml tetramethylurea is added to the reaction mixture, followed by 2 ml water at about 110° C. The mixture is stirred for a further 30 min while cooling to RT and then distributed between dichloromethane and a mixture of 20 ml water and 5 ml conc. ammonia. The organic phase dried over sodium sulfate is concentrated by evaporation and the residue purified on silica gel by flash chromatography using acetate and acetate/methanol (99:1 and 19:1). Title compound is obtained after crystallization of the product-containing fractions from acetonitrile and subsequent recrystallization from acetate; m.p. 141-143° C.; ESI-MS: (M+H)+=327.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06710047B2uspto-grants-2004_03