戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1877507作成日:2026年10月27日

Water → 2-Cyano-5-fluoro-3-(1,2,2,6,6-pentamethylpiperidin-4-yl)aminopyridine

https://huagongshe.com/reaction/1877507

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl AcetateHCID 8857—
反応物4-Amino-1,2,2,6,6-pentamethylpiperidineHCID 693792—
反応物2-Cyano-3,5-difluoropyridineHCID 2783253—
触媒Potassium CarbonateHCID 11430—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-Cyano-5-fluoro-3-(1,2,2,6,6-pentamethylpiperidin-4-yl)aminopyridineHCID 5833835320.5%

反応条件

温度115 °C

反応手順

682 mg of 2-cyano-3,5-difluoropyridine, 995 mg of 4-amino-1,2,2,6,6-pentamethylpiperidine and 1.346 mg of potassium carbonate in 10 ml of dimethyl sulphoxide are introduced into a 20 ml microwave tube reactor. The mixture is then heated in the microwave for 1 hour at 115° C. The reaction medium is run into 100 ml of water and 100 ml of ethyl acetate. The aqueous phase is re-extracted twice with 50 ml of ethyl acetate. The combined organic phases are washed with water and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. After purification by flash chromatography on 70 g of silica gel, elution being carried out with a mixture of dichloromethane, methanol and 4N aqueous ammonia (99/1/0.8 by volume), and the first eluted product being recovered, 290 mg of 2-cyano-5-fluoro-3-(1,2,2,6,6-pentamethylpiperidin-4-yl)aminopyridine are thus obtained in the form of an ecru powder, the characteristics of which are the following:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309721B2
出典データセットuspto-grants-2012_11
ORD IDord-ebbd255367b446169d7e52e2837024fa
出典メモuspto-grants-2012_11