تفاعل #3639

ord-35c9189d6c304adeac0dada394886b55

معادلة التفاعل

O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
c1cc2n(c1)Cc1ccsc1NC2
9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine
CCN(CC)CC
triethylamine
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccsc21
desired product
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccsc21
9,10-Dihydro-10-(4-nitrobenzoyl)-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine

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, 1N HCl, NaHCO3, 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 on silica gel

الإجراء التجريبي

To a solution of 10 mmol of 9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine in 50 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, 1N HCl, NaHCO3, and brine. The organic layer is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography on silica gel to give desired product as a solid.

المصدر

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