تفاعل #1005966

ord-7402d408b2154b1fb88c350284346916

معادلة التفاعل

O=C(OO)c1cccc(Cl)c1
3-chloroperoxybenzoic acid
CCSc1ccccc1-c1cn2cc(C(F)(F)F)ccc2n1
2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
CCS(=O)(=O)c1ccccc1-c1cn2cc(C(F)(F)F)ccc2n1
2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe mixture was extracted with chloroform
  2. 2
    غسيلThe organic layer was washed with a saturated aqueous sodium bicarbonate solution
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

552 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 370 mg of 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine and 5 ml of chloroform under ice cooling, and the mixture was stirred at room temperature for 2 hours. A 10% aqueous sodium thiosulfate solution was poured to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 260 mg of 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine (hereinafter, referred to as Compound of Present Invention 5).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09271500B2uspto-grants-2016_03