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HRID 2117147作成日:2026年10月25日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Methyl 1-(4-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2117147

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物4-FluorobenzylamineHCID 67326—
反応物Methyl 2-oxo-2H-pyran-3-carboxylateHCID 117704—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物Methyl 1-(4-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 2108172273.6%

反応手順

A heterogeneous mixture of methyl 2-oxo-2H-pyran-3-carboxylate (2.0 g, 13 mmol, 1.0 eq, Aldrich) and 4-fluorobenzylamine (1.5 mL, 13 mmol, 1.0 eq) in DMF (10 mL) was stirred at room temperature for 3 h. The reaction mixture was treated with EDCI (3.4 g, 18 mmol, 1.4 eq) and DMAP (0.11 g, 9.91 mmol, 0.07 eq) at room temperature and the resulting solution was stirred for 12 h. The reaction mixture was quenched with 1 N aqueous HCl and the solution was extracted with ethyl acetate (4×50 mL). The combined organic extracts were washed with 10% aqueous LiCl (3×70 mL), dried (Na2SO4), filtered and the filtrate concentrated in vacuo to afford the product (2.5 g, 73%) as a solid, which was used without further purification. 1H NMR (DMSO-d6) δ 8.17-8.20 (m, 1H), 8.03-8.05 (m, 1H), 7.38-7.46 (m, 2H),7.16-7.22 (m, 2H), 6.37 (dd, 1H, J=6.94 Hz), 5.13 (s, 2H), 3.73 (s, 3H); HRMS(ESI): calcd.: 262.0879, found: 262.0885.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07439246B2
出典データセットuspto-grants-2008_10
ORD IDord-144982ab1a93445da490c4fefe1196f8
出典メモuspto-grants-2008_10