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HRID 516726作成日:2026年10月27日

Hydrochloric Acid → 4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/516726

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物OxygenHCID 977—
反応物CyanoacetamideHCID 7898—
反応物Hexen-2-alHCID 12990—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 1564180031.7%

反応手順

To a stirred solution of t-BuOK (22.85 g, 204.08 mmol) and cyanoacetamide (18.8 g, 224.1 mmol) in DMSO (300 mL) was added hex-3-en-2-one (20 g, 204.08 mmol) under argon atmosphere at room temperature. The reaction mixture was then stirred at room temperature for 30 min and then added additional t-BuOK (68.5 g, 612.05 mmol) was added. Argon gas was displaced by oxygen gas and the mixture stirred for 48 hrs at room temperature in presence of oxygen. Reaction was monitored by TLC. The reaction mixture was cooled to 0° C. and diluted with water (100 mL) followed by 4 N HCl (120 mL). The mixture was stirred for 15 min and the resulting solid was filtered. The solid was washed with water (1 L) and dried to afford the title compound, 4-ethyl-1,2-dihydro-6-methyl-2-oxopyridine-3-carbonitrile (10.5 g, 31%), as an off white solid. 1H NMR (CDCl3, 400 MHz): δ ppm 1.148-1.185 (t, 3H, J=7.4 Hz), 2.237 (s, 3H), 2.557-2.614 (m, 2H), 6.211 (s, 1H), 12.330 (broad s, 1H). MS(ES) [M+H]+ 161.06.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09114141B2
出典データセットuspto-grants-2015_08
ORD IDord-931e3b087f9d49a8a4cd60c449ab3cfe
出典メモuspto-grants-2015_08