戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1708190作成日:2026年10月27日

2,4,6-Trimethylpyridine → (4R)-N-(2-Nitrooxyethyl)-2-oxothiazolidine-4-carboxamide

https://huagongshe.com/reaction/1708190

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Nitronium tetrafluoroborateHCID 11073463—
反応物(4R)-N-(2-Hydroxyethyl)-2-oxothiazolidine-4-carboxamideHCID 53943884—
溶媒AcetonitrileHCID 6342—
生成物(4R)-N-(2-Nitrooxyethyl)-2-oxothiazolidine-4-carboxamideHCID 985610113.9%

反応手順

0.44 g of nitronium tetrafluoroborate and a solution of 0.41 g of 2,4,6-collidine in 20 ml of acetonitrile were added at a temperature of from -10° C. to 0° C. to 30 ml of acetonitrile, and the resulting mixture was stirred at the same temperature for 30 minutes. At the end of this time, 0.50 g of (4R)-N-(2-hydroxyethyl)-2-oxothiazolidine-4-carboxamide was added to the mixture, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was then freed from the solvent by distillation under reduced pressure. The residue was mixed with ethyl acetate and insoluble materials were filtered off. The filtrate was concentrated by evaporation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent. The pale yellow crystals thus obtained were recrystallized from ethyl acetate, to give 86 mg of the title compound as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05356918
出典データセットuspto-grants-1994_10
ORD IDord-4377a5b977344fe6ba8cd0d85621ec80
出典メモuspto-grants-1994_10