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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 623422생성일: 2026년 10월 27일

Sodium Bicarbonate → (R)-2-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)propane-2-sulfinamide

https://huagongshe.com/reaction/623422

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Sodium borohydrideHCID 4311764—
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물Ethanone, 1-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-HCID 58629124—
촉매Titanium(IV)ethoxideHCID 2724286—
용매TetrahydrofuranHCID 8028—
생성물(R)-2-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)propane-2-sulfinamideHCID 6751090294%

반응 조건

온도70 °C

반응 단계

A mixture of 1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethanone (4.51 g, 20.58 mmol, Step-3), (R)-2-methylpropane-2-sulfinamide (3.74 g, 30.9 mmol) and tetraethyl orthotitanate (6.47 mL, 30.9 mmol) in tetrahydrofuran (23 mL) is stirred at 70° C. for 17 hours. The reaction mixture is cooled to 0° C., sodium borohydride (2.72 g, 72.0 mmol) is added there, and the mixture is stirred at same temperature for 1 hour. Saturated aqueous sodium hydrogen carbonate (50 mL) is added to the reaction mixture, and the mixture is stirred for 10 minutes. After filtration through a pad of celite (registered trademark), the filtrate is extracted with ethyl acetate (300 mL). The organic layer is washed with water (100 mL×2) and dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (4:1 to 1:1) to give 6.25 g (94% yield) of the title compound as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09302991B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-1bfcdc8639d14458b470d8a6783ffaca
출처 메모uspto-grants-2016_04