반응 #2186221

ord-7bd453fc0daf4f3ea55041f1c5a346dd

반응 방정식

C#CC(N)=O.Nc1c(SC(F)(F)F)c(C(=O)O)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-I H-pyrazole-3-carboxylic acid propargylamide
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
O=C([O-])O.O=S([O-])[O-].[Na+].[Na+].[Na+]
sodium sulfite sodium hydrogen carbonate
C#CC(N)=O.Nc1c(S(=O)C(F)(F)F)c(C(=O)O)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
title compound
수율 86.0%
C#CC(N)=O.Nc1c(S(=O)C(F)(F)F)c(C(=O)O)nn1-c1c(Cl)cc(C(F)(F)F)cc1Cl
5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinyl-1H-pyrazole-3-carboxylic acid propargylamide
수율 86.0%

반응 조건

온도
20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITcontinued for 15 minutes
  3. 3
    추출The aqueous phase was extracted with dichloromethane
  4. 4
    건조dried over magnesium sulfate
  5. 5
    기타evaporated
  6. 6
    기타purified by flash chomatography (silica, heptane/ethyl acetate)

실험 절차

To a suspension of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-I H-pyrazole-3-carboxylic acid propargylamide (0.71 g, 1.43 mmol) in dichloromethane was slowly added a solution of m-chloroperbenzoic acid (70%, 0.41 g, 1.68 mmol) in dichloromethane. After stirring for 17 hours at 20° C., an aqueous solution of sodium sulfite/sodium hydrogen carbonate (5%:5%, 25 ml) was added and stirring continued for 15 minutes. The aqueous phase was extracted with dichloromethane, dried over magnesium sulfate, evaporated and purified by flash chomatography (silica, heptane/ethyl acetate) to give the title compound (0.604 g, yield 86%) as white crystals, mp 207° C., 1H NMR (CDCl3): 2.28 (t, 1H, propargyl), 4.20 (m, 2H, propargyl), 5.17 (bs, 2H, NH2), 6.88 (bt, 1H, C(O)NH), and 7.83 (s, 2H, Ar—H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07569516B2uspto-grants-2009_08