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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1051400생성일: 2026년 10월 25일

Toluene → 1-{2-[5-(4-Chloro-phenyl)-oxazol-2-ylmethyl]-3,3,3-trifluoro-propyl}-3-(3-trifluoromethyl-phenyl)-piperidine

https://huagongshe.com/reaction/1051400

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium CarbonateHCID 10340—
반응물Phosphorus oxychlorideHCID 24813—
반응물N-(2-(4-chlorophenyl)-2-oxoethyl)-4,4,4-trifluoro-3-((3-(3-(trifluoromethyl)phenyl)piperidin-1-yl)methyl)butanamideHCID 90133968—
용매Ethyl AcetateHCID 8857—
생성물1-{2-[5-(4-Chloro-phenyl)-oxazol-2-ylmethyl]-3,3,3-trifluoro-propyl}-3-(3-trifluoromethyl-phenyl)-piperidineHCID 75201374—

반응 조건

온도100 °C

반응 단계

In a 5 mL round-bottomed flask, N-(2-(4-chlorophenyl)-2-oxoethyl)-4,4,4-trifluoro-3-((3-(3-(trifluoromethyl)phenyl)piperidin-1-yl)methyl)butanamide (30 mg, 56.1 μmol) and POCl3 (51.6 mg, 336 μmol) were combined with toluene (1 ml) to give a colorless solution. The reaction mixture was heated to 100° C. and stirred for 4 h. The reaction mixture was diluted with ethyl acetate (30 ml), poured into ice-water and made basic with saturated solution of Na2CO3. The organic layer was separated and washed with brine and H2O, dried over MgSO4, filtered and concentrated in vacuo to give an oil. The resultant oil was purified by flash chromatography (silica gel, 12 g, 0% to 50% ethyl acetate in hexane gradient) to afford 1-{2-[5-(4-chloro-phenyl)-oxazol-2-ylmethyl]-3,3,3-trifluoro-propyl}-3-(3-trifluoromethyl-phenyl)-piperidine as an oil. It was dissolved in Et2O/Hexane, treated with 4N HCl in dioxane (0.1 ml) and concentrated in vacuo to afford 23 mg (76%) of 1-{2-[5-(4-chloro-phenyl)-oxazol-2-ylmethyl]-3,3,3-trifluoro-propyl}-3-(3-trifluoromethyl-phenyl)-piperidine hydrochloride as a white solid. MH+=517.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09388172B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-2ca2c454b95a4d71993a5bf63918575b
출처 메모uspto-grants-2016_07