تفاعل #3632

ord-7d2a5ee88619484c8d74a7550ba9b6d4

معادلة التفاعل

Nc1ccc(C(=O)N2Cc3cccn3Cc3ccoc32)cc1
9,10-dihydro-10-(4-aminobenzoyl)-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine
Cc1ccccc1C(=O)Cl
2-methylbenzoyl chloride
CCN(CC)CC
triethylamine
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccoc32)cc1
desired product
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccoc32)cc1
N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture is washed with water, 1N citric acid, NaHCO3, and brine
  2. 2
    تجفيفThe reaction mixture is dried with Na2SO4
  3. 3
    ترشيحfiltered
  4. 4
    أخرىevaporated in vacuo
  5. 5
    أخرىto give a solid which
  6. 6
    أخرىis purified by flash chromatography on silica gel with ethyl acetate-hexane as solvent

الإجراء التجريبي

To a stirred solution of 1.1 mmol of 2-methylbenzoyl chloride in 10 ml of methylene chloride is added 1.5 mmol of triethylamine. To the mixture is added 1.1 mmol of 9,10-dihydro-10-(4-aminobenzoyl)-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine and the mixture is stirred for 5 hours. The reaction mixture is washed with water, 1N citric acid, 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 on silica gel with ethyl acetate-hexane as solvent to give the desired product as a solid.

المصدر

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