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HRID 411210作成日:2026年10月25日

Diethyl (ethoxymethylene)malonate → Diethyl 2-(((2-(Morpholin-4-ylmethyl)-1,3-thiazol-5-yl)amino)methylene)malonate

https://huagongshe.com/reaction/411210

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (ethoxymethylene)malonateHCID 6871—
反応物2-(Morpholin-4-ylmethyl)-1,3-thiazol-5-amineHCID 22397141—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物Diethyl 2-(((2-(Morpholin-4-ylmethyl)-1,3-thiazol-5-yl)amino)methylene)malonateHCID 2239721586%

反応手順

To a solution of 2-(morpholin-4-ylmethyl)-1,3-thiazol-5-amine (Preparation 27, 1.13 g) in pyridine (10 mL) at 45° C. is added diethyl ethoxymethylenemalonate (2.26 mL). The mixture is stirred overnight, diluted with water (100 mL), and extracted with EtOAc (3×75 mL). The organic layer is dried (MgSO4) and the solvent removed. The residue is purified by column chromatography (eluent 50% EtOAc/hexane) to afford 1.51 g (86%) of the title compound as a brown oil. Physical characteristics: 1H NMR (CDCl3) δ 1.27-1.37, 2.58, 3.72, 3.73, 4.20-4.30, 8.10, 11.02; IR (diffuse reflectance) 1687, 1637, 1596, 1416, 1337, 1301, 1274, 1268, 1243, 1234, 1114, 1094, 1011, 867, 801 cm−1; HRMS (FAB) m/z 370.1420 (C16H23N3O5S+H). Anal. Found: C, 51.80; H, 6.32; N, 11.26.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559145B2
出典データセットuspto-grants-2003_05
ORD IDord-8466d0b4da954502ae6632e5211f861a
出典メモuspto-grants-2003_05