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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442706생성일: 2026년 10월 25일

Triphenylphosphine → 3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-[3-(3-methyl-[1,2,4]oxadiazol-5-yl)phenylethynyl]cyclohexan-1-one

https://huagongshe.com/reaction/442706

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-ethynylcyclohexan-1-oneHCID 15392007—
반응물5-(3-Iodophenyl)-3-methyl-1,2,4-oxadiazoleHCID 19349979—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TriethylamineHCID 8471—
생성물3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-[3-(3-methyl-[1,2,4]oxadiazol-5-yl)phenylethynyl]cyclohexan-1-oneHCID 15434165—

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온도80 °C

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To a solution of the compound from Example 3 (0.125 g, 0.4 mmol) and 1-iodo-3-(3-methyl-[1,2,4]oxadiazol-5-yl)benzene (0.09 g, 0.32 mmol) in triethylamine (3 mL) under an argon atmosphere was added trace tetrakis(triphenylphosphine)-palladium(0), copper(I) iodide and triphenylphosphine. The mixture was heated at 80° C. for 0.2 h, was cooled to room temperature and was concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, was dried (MgSO4) and was evaporated. The residue was purified by flash chromatography, eluting with 2:1 hexanes/ethyl acetate, followed by trituration from hexanes/ethyl acetate, to provide the title compound as a white solid, m.p. 122°-123° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891883
출처 데이터셋uspto-grants-1999_04
ORD IDord-e8c23b57c71c429d9a705583ca8d6623
출처 메모uspto-grants-1999_04