反応 #322835

ord-f64cd5b988b14d4f8e6425d0bb08320b

反応方程式

CCN1CCCC(N)C1
3-Amino-1-ethylpiperidine
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Cl.O=S(=O)(Cl)c1ccc(Nc2cnnc3cc(Cl)ccc23)cc1
4-(7-chloro-4-cinnolinylamino)benzenesulphonylchloride hydrochloride
CCN1CCCC(NS(=O)(=O)c2ccc(Nc3cnnc4cc(Cl)ccc34)cc2)C1
title compound
CCN1CCCC(NS(=O)(=O)c2ccc(Nc3cnnc4cc(Cl)ccc34)cc2)C1
4-[7-Chloro-4-cinnolinylamino]-N-(1-ethyl-3-piperidyl) benzenesulphonamide

反応条件

温度
3°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe dark orange mixture was stirred at 3° C. for 15 minutes
  2. 2
    workup.WAITDuring this period the colour lightened considerably
  3. 3
    その他The chloroform layer was separated
  4. 4
    乾燥dried over magnesium sulphate
  5. 5
    その他The residue on evaporation
  6. 6
    その他triturated with methanol

実験手順

3-Amino-1-ethylpiperidine (0.4 ml) in chloroform (15 ml) was treated with anhydrous sodium carbonate (2.94 g) in water (15 ml) and cooled to 3° C. The mixture was vigorously stirred and treated with 4-(7-chloro-4-cinnolinylamino)benzenesulphonylchloride hydrochloride (1.0 g). The dark orange mixture was stirred at 3° C. for 15 minutes, then at room temperature for 45 minutes. During this period the colour lightened considerably. The chloroform layer was separated and dried over magnesium sulphate. The residue on evaporation solidified when triturated with methanol, to give the title compound (0.5 g), m.p. 213°-15° C. (with decomposition).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04640920uspto-grants-1987_02