تفاعل #3648

ord-3790b2a5481d44819f7ce4004894689f

معادلة التفاعل

O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
c1ccc2c(c1)NCCc1cccn1-2
6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine
CCN(CC)CC
triethylamine
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2cccn2-c2ccccc21
desired product
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2cccn2-c2ccccc21
6,7-Dihydro-5-(4-nitrobenzoyl)-5H-pyrrolo[1,2-a][1,5]benzodiazepine

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfollowed by ice bath
  2. 2
    درجة الحرارةcooling
  3. 3
    workup.ADDITIONaddition
  4. 4
    أخرىthe ice bath is removed
  5. 5
    أخرىThe volatiles are removed in vacuo
  6. 6
    أخرىto give a residue which
  7. 7
    غسيلThe solution is washed with water, 2N citric acid, NaHCO3, and brine
  8. 8
    أخرىThe reaction mixture is dried with Na2 SO4
  9. 9
    ترشيحfiltered
  10. 10
    أخرىevaporated in vacuo
  11. 11
    أخرىto give a solid which
  12. 12
    أخرىis purified by flash chromatography on silica gel

الإجراء التجريبي

To a solution of 10 mmol of 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine in 30 ml of methylene chloride under argon is added 15 mmol of triethylamine followed by ice bath cooling. A solution of 11 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, 2N citric acid, NaHCO3, and brine. The reaction mixture is dried with Na2 SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography on silica gel to give the desired product as a solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733905uspto-grants-1998_03