反応 #3692

ord-917010d59ebf4aef9603f2501a624c6d

反応方程式

O=C(Cl)CCl
chloroacetyl chloride
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]-benzodiazepine
CCN(CC)CC
triethylamine
O=C(CCl)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
beige solid
収率 100.1%
O=C(CCl)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
2-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]acetamide
収率 100.1%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他then partitioned with 10 ml of 50% NaHCO3
  2. 2
    その他the methylene chloride evaporated in vacuo
  3. 3
    ろ過The remaining suspension is filtered
  4. 4
    洗浄washed with 50% NaHCO3, H2O, EtOAc (2×2 ml), ether (2×5 ml)
  5. 5
    その他dried in vacuo

実験手順

To a stirred solution of 0.91 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]-benzodiazepine in 10 ml of methylene chloride is added 0.46 g of triethylamine and 36 mg of dimethylaminopyridine followed by the slow addition of 0.42 g of chloroacetyl chloride in 5 ml of methylene chloride. The resulting mixture is stirred at room temperature for 3 hours then partitioned with 10 ml of 50% NaHCO3 and the methylene chloride evaporated in vacuo. The remaining suspension is filtered, washed with 50% NaHCO3, H2O, EtOAc (2×2 ml), ether (2×5 ml) and dried in vacuo to give 1.14 g of beige solid. MS(CI): 380(M+H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733905uspto-grants-1998_03