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HRID 75772作成日:2026年10月24日

Ethyl 3-(4-aminophenyl)isoxazole-5-carboxylate → HCID 67353512、化合物

https://huagongshe.com/ja/reaction/75772

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 3-(4-aminophenyl)isoxazole-5-carboxylateHCID 53407704—
反応物3-(4-Nitro-phenyl)-5-phenyl-isoxazole-4-carboxylic acid ethyl esterHCID 67353264—
生成物HCID 67353512HCID 67353512—

反応条件

温度80 °C

反応手順

The title compound was prepared using 3-(4-nitro-phenyl)-5-phenyl-isoxazole-4-carboxylic acid ethyl ester by the same procedure as described for the preparation of 3-(4-amino-phenyl)-isoxazol-5-carboxylic acid ethyl ester in Example 1. The reaction mixture was refluxed for 16 hours instead of heating at 80° C. for 3 hours. The crude product was purified by flash chromatography over silica gel with 10% EtOAc in chloroform to give the title compound in 74% yield. IR (KBr): 3374, 1712 (br), 1628, 1610, 1439; 1H NMR (DMSO-d6) δ: 1.15 (t, 3H), 4.20 (q, 2H), 5.57 (s, 2H), 6.63 (d, 2H), 7.34 (d, 2H), 7.53-7.62 (m, 3H), 7.75-7.89 (m, 2H); Mass (ES+), 309 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835428B2
出典データセットuspto-grants-2014_09
ORD IDord-65db4f55613543d984c30967f7bf855e
出典メモuspto-grants-2014_09