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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68368생성일: 2026년 10월 24일

Water → HCID 57415378, 화합물

https://huagongshe.com/ko/reaction/68368

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물[5-(Trifluoromethyl)pyridin-3-yl]boronic acidHCID 45158900—
반응물tert-Butyl[(4aS,5R,7aS)-7a-(5-bromo-2-fluorophenyl)-5-methyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]imidodicarbonateHCID 86707808—
촉매Triphenylphosphine palladium dichlorideHCID 13169693—
용매EthanolHCID 702—
용매1,2-DimethoxyethaneHCID 8071—
용매Sodium BicarbonateHCID 516892—
생성물HCID 57415378HCID 5741537825%

반응 조건

온도100 °C

반응 단계

tert-Butyl[(4aS,5R,7aS)-7a-(5-bromo-2-fluorophenyl)-5-methyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]imidodicarbonate (0.15 g, 0.34 mmol) was dissolved in 1,2-dimethoxyethane (1.5 mL), water (0.7 mL) and ethanol (0.5 mL). The resulting solution was heated to 100° C. and to it was added [5-(trifluoromethyl)pyridin-3-yl]boronic acid (0.32 g, 1.68 mmol), cesium carbonate (0.659 g, 2.02 mmol) and dichloropalladium-triphenylphosphane (0.047 g, 0.067 mmol) and the reaction was stirred at 100° C. After 1 hour, the reaction mixture was cooled to room temperature, diluted with saturated aqueous NaHCO3 and extracted with EtOAc (×3). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo. The residue was purified using column chromatography (gradient 0-60% EtOAc in hexane). The purified product was dissolved in DCM (2 mL) and trifluoroacetic acid (2 L). After 1 hour, the solvents were removed in vacuo. The residue was neutralised with saturated aqueous NaHCO3 and extracted with DCM (×2). The combined organic layers were dried (MgSO4), filtered and concentrated to give the title compound (35 mg, colourless solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822455B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9ce01cdf0d4646c2ad86ada256a3921f
출처 메모uspto-grants-2014_09