反応 #2300

ord-dec26e4a500a423b998283ba15ea943b

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The supernatent was decanted from the solid
  2. 2
    その他formed
  3. 3
    濃縮concentrated in vacuo
  4. 4
    その他purified by flash chromatography on neutral alumina
  5. 5
    洗浄eluting with dichloromethane

実験手順

A solution of methyl 4-chloroacetylphenylacetate (260 mg) in acetonitrile (4 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (375 mg) in acetonitrile (10 ml) and the mixture stirred overnight. The supernatent was decanted from the solid formed, concentrated in vacuo and purified by flash chromatography on neutral alumina, eluting with dichloromethane then 0.25% v/v methanol/dichloromethane and finally 0.5% v/v methanol dichloromethane. Concentration of the fractions in vacuo gave the title compound, 96 mg, as a white crystalline solid: m.p. 127°-129° C.; NMR (d6 DMSO) δ 8.15(2H,d), 7.98(2H,d), 7.41(2H,d), 6.81(2H,d), 3.91(2H,s), 3.78(2H,s), 3.53(3H,s), 3.33(4H,t), 2.64(4H,t); m/e 354(M+H )+ ; calculated for C20H23N3O3 : C, 68.0; H, 6.6; N, 11.9. found: C, 68.2; H, 6.6; N, 11.9%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05728701uspto-grants-1998_03