تفاعل #2028888

ord-a3509b647b3842c88b265ff08cce847b

معادلة التفاعل

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
المردود 25.2%
NS(=O)(=O)c1ccc(-n2nccc2-c2ccc(Cl)cc2)cc1
4-[5-(4-chlorophenyl)-1H-pyrazol-1-yl]benzenesulfonamide
المردود 25.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated
  2. 2
    درجة الحرارةto reflux for 16 hours
  3. 3
    أخرىformed
  4. 4
    أخرىthat were isolated by filtration

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE044048E1uspto-grants-2013_03