تفاعل #3618

ord-bf3f22d548784dd98df4216671f83cda

معادلة التفاعل

O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
c1ccc2c(c1)Cn1ccnc1CN2
10,11-dihydro-5H-imidazo[2,1-c][1,4]benzodiazepine
CCN(CC)CC
triethylamine
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2nccn2Cc2ccccc21
desired product
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2nccn2Cc2ccccc21
10,11-Dihydro-10-(4-nitrobenzoyl)-5H-imidazo[2,1-c][1,4]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, and brine
  8. 8
    تجفيفThe organic layer is dried with Na2SO4
  9. 9
    ترشيحfiltered
  10. 10
    أخرىevaporated in vacuo
  11. 11
    أخرىto give a solid which
  12. 12
    أخرىis purified by flash chromatography

الإجراء التجريبي

To a solution of 10 mmol of 10,11-dihydro-5H-imidazo[2,1-c][1,4]benzodiazepine in 50 ml of methylene chloride under argon is added 15 mmol of triethylamine followed by ice bath cooling. A solution of 10 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, and brine. The organic layer is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography to give desired product as a solid.

المصدر

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