반응 #78174

ord-16b3b8617bca4dd182de9a05e435f45d

반응 조건

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

후처리

  1. 1
    기타has formed
  2. 2
    기타The cooled reaction mixture
  3. 3
    workup.STIRRINGwith thorough stirring
  4. 4
    세척The organic phase washed with water and brine
  5. 5
    건조is dried over anhydrous sodium sulfate
  6. 6
    기타evaporated under vacuum
  7. 7
    기타the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm

실험 절차

A mixture of 910 mg (6.36 mmol) phosphorus pentoxide, 876 mg (6.36 mmol) triethylamine hydrochloride, and 812 mg (6.36 mmol) 4-chloroaniline is heated at 200° C. until a homogeneous melt has formed. To the melt, 400 g (1.59 mmol) 4-[(2-methyl-pyridin-4-yl)-methyl]-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 16 h at 200° C. The cooled reaction mixture is distributed with thorough stirring and use of an ultrasonic bath between a dichloromethane/methanol mixture (about 20:1) and saturated aqueous sodium carbonate solution. The organic phase washed with water and brine is dried over anhydrous sodium sulfate, evaporated under vacuum, and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using an acetate/methanol mixture (19:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and crystallization of the residue from acetonitrile; m.p. 158-159° C.; ESI-MS: (M+H)+=361. The starting material is prepared as follows:

출처

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