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HRID 471753作成日:2026年10月26日

Trimethyl-2-propynylsilane → 2-Amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile

https://huagongshe.com/reaction/471753

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl-2-propynylsilaneHCID 83378—
反応物2-Amino-6-bromobenzonitrileHCID 9813038—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
溶媒TriethylamineHCID 8471—
生成物2-Amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrileHCID 67400216125.2%

反応手順

To a stirred solution of trimethyl(prop-2-ynyl)silane (1.12 g, 10 mmol), 2-amino-6-bromobenzonitrile (Klaubert, D. H.; Sellstedt, J. H.; Guinosso, C. J.; Capetola, R. J.; Bell, S. C. J. Med. Chem. 1981, 24, 742) (1.0 g, 5 mmol), CuI (0.01 equiv.) in triethylamine (50 mL) was added Pd(PPh3)4 (0.1 equiv.) at room temperature under nitrogen. The reaction mixture was then refluxed under nitrogen overnight. The solvent was evaporated, and the residue was titrated with EtOAc/water. The organic layer was separated, were washed with brine, and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 15% EtOAc in hexanes to give the title compound (1.43 g, 63%) as a as a liquid. MS 229 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633186B2
出典データセットuspto-grants-2014_01
ORD IDord-b169c76aac034637bdeed3ed70a44150
出典メモuspto-grants-2014_01