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HRID 1178573作成日:2026年10月27日

Diisopropyl Ether → 1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanone

https://huagongshe.com/reaction/1178573

反応式

関与物質

役割名称HCID仕込み量
反応物Diisopropyl EtherHCID 7914—
反応物TetrahydrofuranHCID 8028—
反応物HexaneHCID 8058—
反応物tert-butyl N-(4-methylpyridin-2-yl)carbamateHCID 11063648—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
生成物1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanoneHCID 1161709269%

反応条件

温度-78 °C

反応手順

A solution of 2-tert-butoxycarbonylamino-4-methylpyridine (20 g, 97 mmol) in anhydrous tetrahydrofuran (300 mL) was cooled to −78° C. and a solution of 1.6 M n-butyllithium in hexane (140 mL, 0.22 mol) was added dropwise with stirring. After complete addition, the mixture was stirred at room temperature for 30 minutes. And then, the mixture was cooled to −78° C. A solution of N-(4-methoxybenzoyl)propyleneimine in anhydrous tetrahydrofuran (50 mL) was added dropwise to the mixture. After complete addition, the mixture was stirred at room temperature for 2 hours. Water (100 mL) and diisopropyl ether (300 mL) were added to the reaction mixture and the resulting crude crystals were collected by filtration. The crude crystals were recrystallized from tetrahydrofuran-hexane to obtain 23 g of the title compound (67 mmol, yield 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07276527B2
出典データセットuspto-grants-2007_10
ORD IDord-b48b84cf9965492cb367662e8a36f82e
出典メモuspto-grants-2007_10