반응 #1583814

ord-0c546883ac6a4eeb9386a2bcfbc1e624

반응 방정식

OO
hydrogen peroxide
CCc1nc(-c2ccc(F)cc2)c(-c2ccncc2)s1
4-[2-ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine
CCc1nc(-c2ccc(F)cc2)c(-c2cc[n+]([O-])cc2)s1
desired product
수율 85.0%
CCc1nc(-c2ccc(F)cc2)c(-c2cc[n+]([O-])cc2)s1
4-[2-Ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine 1-oxide
수율 85.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타does not exceed 15° C.
  2. 2
    세척the organic phase is washed successively with 30 ml of a saturated aqueous NaHCO3 solution, 30 ml of a saturated Na2SO3 solution and 30 ml of water
  3. 3
    건조dried over MgSO4

실험 절차

3.9 ml (44 mmol) of a 30% strength hydrogen peroxide solution are added dropwise with cooling to a solution of 2.18 g (7.24 mmol) of 4-[2-ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine and 46.2 mg (0.19 mmol) of methyltrioxorhenium (VII) in 10 ml dichloromethane such that the temperature of the reaction mixture does not exceed 15° C., and the mixture is stirred at room temperature for 16 h. The reaction mixture is then diluted with 100 ml of dichloromethane, and the organic phase is washed successively with 30 ml of a saturated aqueous NaHCO3 solution, 30 ml of a saturated Na2SO3 solution and 30 ml of water and dried over MgSO4. Under reduced pressure, the product is freed from the solvent, giving 1.98 g (85%) of the desired product; 1H-NMR(DMSO-d6) δ: 8.12 (d, 2H), 7.53 (m, 2H), 7.25 (d, 2H), 7.21 (m, 2H), 3.03 (q, 2H), 1.36 (t, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09198426B2uspto-grants-2015_12