反応 #3622

ord-753e4a858f2c476d8ba39b9fa7affcdf

反応方程式

O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
c1ccc2c(c1)NCc1cccn1-2
4,5-dihydropyrrolo[1,2-a]quinoxaline
CCN(CC)CC
triethylamine
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2-c2ccccc21
desired product
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2-c2ccccc21
4,5-Dihydro-5-(4-nitrobenzoyl)pyrrolo[1,2-a]quinoxaline

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他followed by ice bath
  2. 2
    温度cooling
  3. 3
    workup.ADDITIONaddition
  4. 4
    その他the ice bath is removed
  5. 5
    その他The volatiles are removed in vacuo
  6. 6
    その他to give a residue which
  7. 7
    洗浄The solution is washed with water, 1N HCl, NaHCO3, and brine
  8. 8
    乾燥The reaction mixture is dried with Na2SO4
  9. 9
    ろ過filtered
  10. 10
    その他evaporated in vacuo
  11. 11
    その他to give a solid which
  12. 12
    その他is purified by flash chromatography

実験手順

To a solution of 5 mmol of 4,5-dihydropyrrolo[1,2-a]quinoxaline in 50 ml of methylene chloride under argon is added 10 mmol of triethylamine followed by ice bath cooling. A solution of 5 mmol of 4-nitrobenzoyl chloride in 10 ml of methylene chloride is added dropwise. Following complete addition, the ice bath is removed and the reaction mixture stirred at room temperature for 2 hours. The volatiles are removed in vacuo to give a residue which is dissolved in ethyl acetate. The solution is washed with water, 1N HCl, NaHCO3, and brine. The reaction mixture is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography to give the desired product (from ethyl acetate) as a solid, m.p. 174°-178° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733905uspto-grants-1998_03