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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445810생성일: 2026년 10월 26일

Sodium Carbonate → 2-(4'-Methanesulfinyl-biphenyl-4-yl)-5-methyl-4-(2-pyrrolidin-1-yl-ethyl)-oxazole

https://huagongshe.com/reaction/1445810

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물(4-(Methylsulfinyl)phenyl)boronic acidHCID 2773531—
반응물2-(4-Bromo-phenyl)-5-methyl-4-(2-pyrrolidin-1-yl-ethyl)-oxazoleHCID 11681546—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물2-(4'-Methanesulfinyl-biphenyl-4-yl)-5-methyl-4-(2-pyrrolidin-1-yl-ethyl)-oxazoleHCID 1166836530.3%

반응 단계

To a stirred solution of 2-(4-Bromo-phenyl)-5-methyl-4-(2-pyrrolidin-1-yl-ethyl)-oxazole (50 mg, 0.149 mmol), sodium carbonate (47.5 mg, 0.448 mmol) and 4-Methylsulfinylbenzene boronic acid (137.3 mg, 0.75 mmol) in toluene (2.5 mL), water (0.75 mL) and ethanol (1 mL) under nitrogen was added Tetrakis(triphenylphosphine) palladium (0) (17. 2 mg, 0.015 mmol). The reaction was then heated to reflux for 48 h. The reaction was allowed to cool and bound to a SCX-2 cartridge (5 g). The cartridge was washed with one cartridge volume of dimethylformamide and two volumes of methanol. The product was eluted using 2M ammonia in methanol. The ammonia/methanol solution was evaporated on a Genevac® HT4. The sample was further purified by prep-LCMS. The resulting acetonitrile/water fractions were combined and evaporated using a Genevac® HT4 to give 17.8 mg of a colourless oil (30%). MS (m/e): 395.2 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666871B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-62040ce2fea94c37b7258bfd3a19f6ab
출처 메모uspto-grants-2010_02