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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732196생성일: 2026년 10월 25일

Water → Methyl 3-[4-({4-[((3-methylbutyl){4-[4-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}amino)methyl]-benzyl)oxy)phenyl]propanoate

https://huagongshe.com/reaction/732196

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-(4-([4-(chloromethyl)benzyl]oxy)phenyl)propanoateHCID 23082857—
반응물N-(3-Methylbutyl)-4-[4-(trifluoromethyl)phenyl]-1,3-thiazol-2-amineHCID 23143261—
용매DimethylformamideHCID 6228—
생성물Methyl 3-[4-({4-[((3-methylbutyl){4-[4-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}amino)methyl]-benzyl)oxy)phenyl]propanoateHCID 2314328957%

반응 단계

To a solution of N-(3-methylbutyl)-4-[4-(trifluoromethyl)phenyl]-1,3-thiazole-2-amine (500 mg, 1.59 mmol) in N,N-dimethylformamide (10 mL) was added 60% sodium hydride (63.6 mg, 1.59 mmol) and the mixture was stirred for 30 min. Methyl 3-(4-{[4-(chloromethyl)benzyl]oxy}phenyl)propanoate (462 mg, 1.45 mmol) was added and the obtained mixture was stirred at room temperature for 13 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-40:60) to give the title compound (490 mg, yield 57%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585880B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-ef1bb3c0697b493ca71438db3a9fc9d6
출처 메모uspto-grants-2009_09