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HRID 237349作成日:2026年10月25日

3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester → Methyl-4-(2-fluoro-4-iodo-phenylamino)-2,3-dihydro-thiophene-3-carboxylate

https://huagongshe.com/reaction/237349

反応式

関与物質

役割名称HCID仕込み量
反応物3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl esterHCID 98424—
反応物2-Fluoro-4-iodoanilineHCID 185694—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
生成物Methyl-4-(2-fluoro-4-iodo-phenylamino)-2,3-dihydro-thiophene-3-carboxylateHCID 6661758042%

反応手順

A solution of methyl-4-oxo-tetrahydro-thiophene-3-carboxylate (5.75 g, 35.9 mmol) and 2-fluoro-4-iodo-aniline (9.4 g, 40.9 mmol) were heated to reflux in a mixture of ethanol (25 mL) and acetic acid (0.3 mL) for 18 hours. The solution was cooled to room temperature, filtered and the solid product dried in vacuo to provide methyl-4-(2-fluoro-4-iodo-phenylamino)-2,3-dihydro-thiophene-3-carboxylate (5.70 g, 42% yield). MS (EI) for C12H11FINO2S: 380 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642584B2
出典データセットuspto-grants-2014_02
ORD IDord-2b0c61ca66c2446087e7accda5ed23b4
出典メモuspto-grants-2014_02