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HRID 75939作成日:2026年10月23日

Iodine → 2,6-Dichloro-5-fluoro-4-iodonicotinonitrile

https://huagongshe.com/ja/reaction/75939

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物DiisopropylamineHCID 7912—
反応物Sodium ThiosulfateHCID 24477—
反応物Lithium diisopropylamideHCID 2724682—
反応物2,6-Dichloro-5-fluoro-3-pyridinecarbonitrileHCID 2733849—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2,6-Dichloro-5-fluoro-4-iodonicotinonitrileHCID 8662062387.5%

反応条件

温度-78 °C

反応手順

To a solution of diisopropylamine (15.9 g, 157 mmol) in THF (400 ml) at −78° C. was added n-butyllithium (2.5 M hexanes, 154 mmol), and the solution was stirred at −78° C. for 30 minutes. The lithium diisopropylamide solution was then added slowly dropwise to a −78° C. solution of 2,6-dichloro-5-fluoronicotinonitrile (10.0 g, 52.3 mmol) and iodine (26.5 g, 104 mmol) in THF (175 ml). Upon completion of the addition, the reaction was allowed to warm slowly to room temperature, and stirred at room temperature for 12 hours. An aqueous 10% Na2S2O3 solution (500 ml) was added and the reaction was extracted with EtOAc (3×300 ml). The combined organic fractions were dried over Na2SO4, filtered, and then concentrated to give the title compound (14.5 g, 87%) as a brown solid that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835465B2
出典データセットuspto-grants-2014_09
ORD IDord-808231e5a3284e5489291033d5ce8883
出典メモuspto-grants-2014_09