반응 #172126

ord-fad7574bf7b346bd8d9f520537762d70

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타In a flask under nitrogen was placed
  2. 2
    온도cooled
  3. 3
    workup.STIRRINGstirred for 15 minutes
  4. 4
    여과The mixture was filtered
  5. 5
    세척the precipitate washed with 25 mL of ethyl acetate
  6. 6
    농축The filtrate was concentrated

실험 절차

In a flask under nitrogen was placed tris(dibenzylideneacetone)dipalladium(0) (313 mg, 0.34 mmol) in 25 mL of 1,4-dioxane followed by the product obtained from Example 97A (4.5 g, 16.7 mmol), N-methyldicyclohexylamine (3.91 g, 20.0 mmol), tri-tert-butylphosphine (0.68 mL of a 1.0 M solution in toluene, 0.68 mmol) and acrylonitrile (1.06 g, 20.0 mmol). The mixture was stirred and heated at 50° C. under nitrogen for 90 minutes and then cooled and diluted with 100 mL of ethyl acetate and stirred for 15 minutes. The mixture was filtered and the precipitate washed with 25 mL of ethyl acetate. The filtrate was concentrated and worked up as described in Example 55B to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.92 (s, 3H) 6.55 (d, J=17.29 Hz, 1H) 7.54-7.66 (m, 2H) 8.13-8.25 (m, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846951B2uspto-grants-2014_09