反応 #2028888

ord-a3509b647b3842c88b265ff08cce847b

反応方程式

O=CCC(=O)c1ccc(Cl)cc1
3-[4-(Chloro)phenyl]-propane-1,3-dione
O=CCC(=O)c1ccc(Cl)cc1
3-[4-(chloro)phenyl]-propane-1,3-dione
Cl.NNc1ccc(S(N)(=O)=O)cc1
4-sulfonamidophenylhydrazine hydrochloride
c1cn[nH]c1
pyrazole
NS(=O)(=O)c1ccc(-n2nccc2-c2ccc(Cl)cc2)cc1
white solid
収率 25.2%
NS(=O)(=O)c1ccc(-n2nccc2-c2ccc(Cl)cc2)cc1
4-[5-(4-chlorophenyl)-1H-pyrazol-1-yl]benzenesulfonamide
収率 25.2%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度heated
  2. 2
    温度to reflux for 16 hours
  3. 3
    その他formed
  4. 4
    その他that were isolated by filtration

実験手順

3-[4-(Chloro)phenyl]-propane-1,3-dione from Step 1 (18.3 g, 0.1 mol) and 4-sulfonamidophenylhydrazine hydrochloride (22.4 g, 0.1 mol) were dissolved in 150 mL of absolute ethanol and heated to reflux for 16 hours. The solution was cooled to room temperature, diluted with 100 mL of water and let stand, whereupon crystals of pyrazole formed that were isolated by filtration to provide 8.4 g (25%) of a white solid: mp 185°-187° C.; 1H NMR (CDCl3/300 MHz) 7.89 (d, J=8.7Hz, 2H), 7.76 (d, J=1.8Hz, 1H), 7.43 (d,J=8.7Hz, 2H), 7.34 (d, J=8.7Hz, 2H), 7.17 (d, J=8.7Hz, 2H), 6.53 (d, J=1.8Hz, 1H), 4.93 (brs 2H). Anal. Calc'd for C15H12N3SO2Cl: C, 53.97; H, 3.62; N, 12.59. Found: C, 54.08; H, 3.57; N, 12.64.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE044048E1uspto-grants-2013_03