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HRID 1064415作成日:2026年10月27日

Water → Tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamate

https://huagongshe.com/reaction/1064415

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PhenolHCID 996—
反応物Sodium hydrideHCID 24758—
反応物Tert-butyl 2-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]ethylcarbamateHCID 21973801—
溶媒DiglymeHCID 8150—
生成物Tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamateHCID 2197382359.1%

反応条件

温度90 °C

反応手順

Phenol (1.19 g, 12.6 mmol) was added in portions to a chilled (0° C.) suspension of sodium hydride (0.52 g of 60%, 13.1 mmol) in diglyme (4 mL). The reaction mixture was then stirred for 30 minutes. A warm solution of tert-butyl 2-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]ethylcarbamate (3.0 g, 8.70 mmol) in diglyme (6 mL) was added and the reaction mixture was heated at 90° C. overnight. The reaction mixture was cooled and poured slowly into water (100 mL). The resulting tan solid was isolated by filtration, washed with water, dried and then recrystallized from isopropanol (25 mL) to provide 2.07 g of tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamate as white needles. The reaction was repeated using 66.5 g of starting material to provide 50.4 g of product as white needles, m.p. 158-160° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06969722B2
出典データセットuspto-grants-2005_11
ORD IDord-2863eaa1ce8d4c9f8f10645bc10c028f
出典メモuspto-grants-2005_11