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HRID 11984作成日:2026年10月25日

Triethylamine → 2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2'-iodo-6'-methoxyphenyl)acetamide

https://huagongshe.com/reaction/11984

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Chloro-1-methylpyridinium iodideHCID 167069—
反応物2-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)acetic acidHCID 11287090—
反応物2-Iodo-6-methoxyanilineHCID 11379663—
溶媒DichloromethaneHCID 6344—
生成物2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2'-iodo-6'-methoxyphenyl)acetamideHCID 2195169089.6%

反応手順

A solution of (1,4-dioxaspiro[4.5]dec-7-en-8-yl) acetic acid (567 mg; 2.86 mmol; 1 eq) (7) and 2-iodo-6-methoxyaniline (1 g; 2.86 mmol; 1 eq) in anhydrous dichloromethane (30 mL) is admixed with 2-chloro-1-methylpyridinium iodide (1.46 g; 5.73 mmol; 2 eq) and triethylamine (3.98 mL; 28.65 mmol; 10 eq). The reaction mixture is heated at reflux for 20 hours. After cooling and acidification with 1N HCl solution to pH=5-6, the mixture is extracted with dichloromethane. The organic phases are washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and evaporated under vacuum. Purification by flash chromatography on silica gel (eluent: heptane/ethyl acetate 4/6) gives 1.10 g of 2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2′-iodo-6′-methoxy-phenyl)acetamide (16) in the form of a yellow foam (yield: 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE041366E1
出典データセットuspto-grants-2010_06
ORD IDord-d73a86df4d0d4a32a23007aeff1a94e4
出典メモuspto-grants-2010_06