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HRID 442706作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-ethynylcyclohexan-1-oneHCID 15392007—
反応物5-(3-Iodophenyl)-3-methyl-1,2,4-oxadiazoleHCID 19349979—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TriethylamineHCID 8471—
生成物3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-[3-(3-methyl-[1,2,4]oxadiazol-5-yl)phenylethynyl]cyclohexan-1-oneHCID 15434165—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05891883
出典データセットuspto-grants-1999_04
ORD IDord-e8c23b57c71c429d9a705583ca8d6623
出典メモuspto-grants-1999_04