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HRID 563946作成日:2026年10月27日

3-Aminopyridine → N-pyridin-3-ylpyridin-3-amine

https://huagongshe.com/reaction/563946

反応式

関与物質

役割名称HCID仕込み量
反応物3-AminopyridineHCID 10009—
反応物3-BromopyridineHCID 12286—
反応物Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物N-pyridin-3-ylpyridin-3-amineHCID 59877584.4%

反応手順

To a solution of 3-bromopyridine (4.75 gm, 30 mmol) and 3-aminopyridine (1.88 gm, 20 mmol) in dry toluene (8 mL) was added sodium t-butoxide (2.3 gm, 24 mmol), tris(dibenylideneacetone) dipalladium(0) (63 mg, 0.069 mmol), and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (XANTPHOS) (183 mg, 0.317 mmol). The vessel was capped with a septum, degassed (3×), and heated at 100 C for ˜24 hours. The cooled reaction was diluted with methylene chloride, washed with NaHCO3 solution, water, and the organic layer dried over anhydrous sodium sulfate, filtered and the solvent concentrated to a small volume. Upon addition of diethyl ether and a few drops of methanol the product precipitated. After stirring this mixture for ˜15 hours the purified product was isolated by filtration to give 2.89 gm (84% yield) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067607B2
出典データセットuspto-grants-2011_11
ORD IDord-33bd4cb3980b4265898ae7d7d3085f54
出典メモuspto-grants-2011_11