반응 #46596

ord-1395cd279e864ba28644241d779103fc

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도to reflux under N2 overnight
  3. 3
    여과The dark mixture was filtered through a pad of Celite®
  4. 4
    세척the filter pad was rinsed with acetonitrile (250 mL)
  5. 5
    농축The filtrate was concentrated in vacuo
  6. 6
    기타the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3)

실험 절차

A solution of 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (0.64 g, 2.80 mmole), N-(1H-indol-3-ylmethyl)-N-methylacrylamide (0.60 g, 2.80 mmole), Pd(OAc)2 (0.06 g, 0.28 mmole), tri-ortho-tolylphosphine (0.17 g, 0.56 mmole) and diisopropylethylamine (0.73 mL, 4.2 mmole) in propionitrile (50 mL) was deoxygenated, then was heated to reflux under N2 overnight. The dark mixture was filtered through a pad of Celite®, and the filter pad was rinsed with acetonitrile (250 mL). The filtrate was concentrated in vacuo, and the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3). The title compound (0.37 g, 37%) was obtained as a light yellow solid after drying in vacuo: MS (ES) m/e 361 (M+H)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741339B2uspto-grants-2010_06