تفاعل #3642

ord-e2444919c6b4455d88ef28dab32fb982

معادلة التفاعل

Cc1ccccc1C(=O)Cl
2-methylbenzoyl chloride
CCN(CC)CC
triethylamine
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccsc32)cc1
9,10-dihydro-10-(4-aminobenzoyl)-4H-pyrrolo-[1,2-a]thieno[2,3-e][1,4]diazepine
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccsc32)cc1
desired product
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccsc32)cc1
N-[4-(4H-Pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepin-10(9H)-ylcarbonyl)phenyl]-2-methylbenzamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture is washed with water, 2N citric acid, NaHCO3, and brine
  2. 2
    تجفيفThe organic layer 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

الإجراء التجريبي

To a stirred solution of 5 mmol of 2-methylbenzoyl chloride in 10 ml of methylene chloride is added 7 mmol of triethylamine and 5 mmol of 9,10-dihydro-10-(4-aminobenzoyl)-4H-pyrrolo-[1,2-a]thieno[2,3-e][1,4]diazepine and the mixture stirred for 5 hours. The reaction mixture is washed with water, 2N citric acid, 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 the desired product as a solid.

المصدر

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