반응 #3652

ord-7ff22cdac5b94a6fa902c99d2482bd2d

반응 방정식

Cc1ccccc1C(=O)Cl
2-methylbenzoyl chloride
CCN(CC)CC
triethylamine
Nc1ccc(C(=O)N2CCc3cccn3-c3ccccc32)cc1
6,7-dihydro-5-(4-aminobenzoyl)-5H-pyrrolo[1,2-a][1,5]benzodiazepine
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCc3cccn3-c3ccccc32)cc1
desired product
Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCc3cccn3-c3ccccc32)cc1
N-[4-[(6,7-Dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepin-5-yl)carbonyl)phenyl]-2-methyl-benzamide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척The reaction mixture is washed with water, 2M citric acid, NaHCO3, and brine
  2. 2
    건조The organic layer is dried with Na2SO4
  3. 3
    여과filtered
  4. 4
    기타evaporated in vacuo
  5. 5
    기타to give a solid which
  6. 6
    기타is purified by flash chromatography on silica gel

실험 절차

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 6,7-dihydro-5-(4-aminobenzoyl)-5H-pyrrolo[1,2-a][1,5]benzodiazepine. The reaction mixture is washed with water, 2M 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; mass spectrum (CI): 422(M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733905uspto-grants-1998_03