تفاعل #11886

ord-7e15299e24944a1ea8f3d98132393c75

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture was washed with hexanes (50 mL×3)
  2. 2
    أخرىthe supernatant was decanted off after each time
  3. 3
    workup.DISSOLUTIONThe residue was then dissolved in ethyl acetate (100 mL)
  4. 4
    غسيلsuccessively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL)
  5. 5
    تجفيفdried over anhydrous sodium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىThe residue was then purified by flash column chromatography

الإجراء التجريبي

A mixture of 3-(2,4-dichloro-pyrimidin-5-yl)-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester (440 mg, 1.1 mmol) (from Example 11a supra) and aniline (2.0 mL) (Aldrich) was heated at 110° C. for 2 hours. The reaction mixture was washed with hexanes (50 mL×3) and the supernatant was decanted off after each time. The residue was then dissolved in ethyl acetate (100 mL) and successively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was then purified by flash column chromatography to give the crude 3-(2,4-diphenylamino-pyrimidin-5-yl)-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester as an off-white solid. (Yield 470 mg, 86%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07098332B2uspto-grants-2006_08