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HRID 77797作成日:2026年10月26日

Water → 3-((Trimethylsilyl)ethynyl)pyridin-2-amine

https://huagongshe.com/reaction/77797

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TrimethylsilylacetyleneHCID 66111—
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-3-bromopyridineHCID 817700—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物3-((Trimethylsilyl)ethynyl)pyridin-2-amineHCID 5747566694.3%

反応条件

温度70 °C

反応手順

To a solution of 2-amino-3-bromopyridine (5.72 g, 33.1 mmol) in N-methylpyrrolidinone (120 mL) were added trimethylsilyl acetylene (9.36 mL, 66.2 mmol), tetrakis(triphenylphosphine)palladium (0) (1.91 g, 1.66 mmol), copper (I) iodide (630 mg, 3.31 mmol) and N,N-diisopropylethylamine (11.5 mL, 66.2 mmol) at room temperature, which was stirred under nitrogen atmosphere for 6 hours at 70° C. Water was added to the reaction solution, which was then extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the title compound (5.94 g, 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-1037695923d3435a9d15a1f5f3ee14cc
出典メモuspto-grants-2014_09