戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 347540作成日:2026年10月26日

3-Aminopyridine → Methyl 2-oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/347540

反応式

関与物質

役割名称HCID仕込み量
反応物3-AminopyridineHCID 10009—
反応物Methyl 2-oxo-2H-pyran-3-carboxylateHCID 117704—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylateHCID 2108172672.4%

反応手順

To a solution of methyl 2-oxo-2H-pyran-3-carboxylate (462 mg, 3 mmol, Aldrich) in DMF (6 mL) at rt was added 3-aminopyridine (282 mg, 3 mmol). The reaction mixture was stirred at rt for 12 h and treated with EDCI.HCl (650 mg, 3.4 mmol) and DMAP (200 mg). The reaction mixture was stirred for 2.5 days at rt, and most of the DMF was removed in vacuo. The residue was purified by preparative HPLC to afford the desired product (500 mg, 72%) as a glassy material. 1H NMR (CDCl3) δ 8.53 (d, 1H, J=5.0 Hz), 8.20 (dd, 1H, J=9.2, 2.2 Hz), 8.06 (dd, 1H, J=6.0, 1.1 Hz), 7.89–7.82 (m, 2H), 7.32 (dd, 1H, J=6.6, 5.0 Hz), 6.36 (t, 1H, J=6.6 Hz), 3.86 (s, 3H); MS(ESI+) m/z 231.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173031B2
出典データセットuspto-grants-2007_02
ORD IDord-2e3a6493ad854b05b7f49e29a62bab58
出典メモuspto-grants-2007_02