戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 45405作成日:2026年10月23日

Pyridine → Ethyl 2-benzamido-4-methylthiazole-5-carboxylate

https://huagongshe.com/ja/reaction/45405

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzoyl chlorideHCID 7412—
反応物Ethyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-benzamido-4-methylthiazole-5-carboxylateHCID 68399197%

反応手順

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (2.00 g, 10.00 mmol) in anhydrous dichloromethane (40 mL) was added pyridine (2.50 g, 32.00 mmol), followed by the addition of benzoyl chloride (1.90 g, 13.00 mmol) dropwise. The reaction mixture was stirred at ambient temperature for 18 h, then washed sequentially with 1 N hydrochloric acid (15 mL), saturated aqueous sodium bicarbonate (2×15 mL), and water (15 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was purified by column chromatography to afford the title compound as a white solid in 97% yield (3.0 g); 1H NMR (CDCl3, 300 MHz) δ 11.35 (s, br, 1H), 7.89 (d, J=7.4 Hz, 2H), 7.59 (t, J=7.4 Hz, 1H), 7.47 (t, J=7.6 Hz, 2H), 4.29 (q, J=7.1 Hz, 2H), 2.28 (s, 3H), 1.35 (t, J=7.1 Hz, 3H); MS (ES+) m/z 291.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541457B2
出典データセットuspto-grants-2013_09
ORD IDord-a688f488a9d64955b03427bc47f03263
出典メモuspto-grants-2013_09