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HRID 77833作成日:2026年10月24日

Trimethylsilylacetylene → 2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-

https://huagongshe.com/ja/reaction/77833

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilylacetyleneHCID 66111—
反応物3-Iodopyridine-2,6-diamineHCID 476218—
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2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-HCID 5925547160%

反応手順

To a mixture of 3-iodo-pyridin-2,6-diamine (20.0 g, 85.2 mmol) described in Manufacturing Example 13-1-1, trimethylsilyl acetylene (24.2 mL, 170 mmol), copper (I) iodide (3.25 g, 17.0 mmol) N,N-diisopropylethylamine (19.1 g, 148 mmol) and N-methylpyrrolidinone (286 mL) was added tetrakis(triphenylphosphine)palladium (0) (9.81 g, 8.52 mmol) under argon atmosphere, which was stirred for 30 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The ethyl acetate layer was washed with water 4 times and dried over sodium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel chromatography (heptane:ethyl acetate=4:1 then 1:1). The solids obtained by concentrating the eluate under a reduced pressure were washed with heptane containing a small amount of ethyl acetate to obtain the title compound (10.5 g, 60.0%).

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-8b516c37d4ea4c2baa72aa8bf98345ef
出典メモuspto-grants-2014_09