反応 #46610

ord-7521f4df9bb640d88cf03f314724404e

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction was heated
  2. 2
    温度at reflux under argon for 10 h
  3. 3
    ろ過filtered through supercel
  4. 4
    濃縮The filtrate was concentrated
  5. 5
    その他the residue was purified by flash chromatography on silica gel

実験手順

A mixture of N-methyl-N-(1,2,7-trimethyl-1H-indol-3-ylmethyl)acrylamide (256 mg, 1 mmole) and 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (227 mg, 1 mmole) in propionitrile (20 mL) was treated with DIEA (0.3 mL), Pd(OAc)2 (29 mg, 0.13 mmole), and tri-o-tolylphosphine (50 mg, 0.16 mmole). The reaction was heated at reflux under argon for 10 h, then was cooled to RT and filtered through supercel. The filtrate was concentrated and the residue was purified by flash chromatography on silica gel to afford the title compound (100 mg, 25%) as an off-white solid: MS (ES) m/e 403.2 (M+H)+. Anal. Calcd for C24H26N4O2.2.75H2O: C, 63.77; H, 7.02; N, 12.39. Found: C, 63.81; H, 7.25; N, 11.90.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741339B2uspto-grants-2010_06