反応 #1372622

ord-00f2d85bf9d44e13b1808a40929e5695

反応方程式

CCC(C(O)c1ccc2c(c1)CCC(=O)N2)N1CCNCC1
6-(1-hydroxy-2-piperazinylbutyl)-3,4-dihydrocarbostyril
O=[N+]([O-])Nc1ccc(Br)cc1
p-bromonitroaniline
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C1CCc2ccccc2N1
3,4-dihydrocarbostyril

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度refluxed
  2. 2
    温度by heating for 5 hours
  3. 3
    ろ過The reaction mixture was filtered
  4. 4
    濃縮the mother liquor was concentrated by distillation under a reduced pressure to dryness
  5. 5
    その他The residue thus obtained
  6. 6
    抽出was extracted with methanol-chloroform
  7. 7
    その他the solvent was removed by distillation
  8. 8
    その他to obtain a residue
  9. 9
    その他The residue was purified
  10. 10
    その他separated by a preparative silica-gel thin layer chromatograph

実験手順

5.0 Grams of 6-(1-hydroxy-2-piperazinylbutyl)-3,4-dihydrocarbostyril, 3.5 g of p-bromonitroaniline, 1.8 g of potassium carbonate and 0.2 g of copper powder were mixed in 60 ml of 3-methoxybutanol and refluxed by heating for 5 hours. The reaction mixture was filtered and the mother liquor was concentrated by distillation under a reduced pressure to dryness. The residue thus obtained was extracted with methanol-chloroform and the solvent was removed by distillation to obtain a residue. The residue was purified and separated by a preparative silica-gel thin layer chromatograph to obtain 0.21 g of 6-{1-hydroxy-2-[4-nitrophenyl)-1-piperazinyl]butyl}-3,4-dihydrocarbostyril in yellow powdery crystals.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04567187uspto-grants-1986_01