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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 914350생성일: 2026년 10월 25일

Water → 2-Methyl-2-({4-[2-({5-[3-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)ethyl]-1,3-thiazol-2-yl}thio)propionic acid tert-butyl ester

https://huagongshe.com/reaction/914350

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물HCID 22283558HCID 22283558—
반응물2-[(4-{2-[(5-Bromopyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl esterHCID 59758804—
촉매HCID 178418397HCID 178418397—
용매Sodium CarbonateHCID 10340—
용매1,4-DioxaneHCID 31275—
생성물2-Methyl-2-({4-[2-({5-[3-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)ethyl]-1,3-thiazol-2-yl}thio)propionic acid tert-butyl esterHCID 5975933991.9%

반응 단계

Under nitrogen atmosphere, 2-[(4-{2-[(5-bromopyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester (920 mg) synthesized in Example 162-1 and 3-(trifluoromethyl)phenylboric acid (380 mg) were dissolved in dioxane (10 mL) and 2 mol/L sodium carbonate (5 mL), tetrakis(triphenylphosphine)palladium (115 mg) was added, and the mixture was refluxed for 4 hr. The reaction mixture was cooled, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate=5:1 to 2:1) to give the title compound (890 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026370B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-87e393a3bdf0492bb0e23df698e7f679
출처 메모uspto-grants-2011_09