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HRID 7070作成日:2026年10月23日

Pentafluorophenol → N-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamide

https://huagongshe.com/ja/reaction/7070

反応式

関与物質

役割名称HCID仕込み量
反応物PentafluorophenolHCID 13041—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物N-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamideHCID 22019637—
溶媒DichloromethaneHCID 6344—
生成物N-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamideHCID 2201959894.7%

反応条件

温度25 °C

反応手順

A mixture of N-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamide (500 mg), pentafluorophenol (305 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (320 mg) and methylene chloride (10 ml) is stirred at 25° C. for 18 hours. The reaction solution is washed with water, and the solvent is evaporated under reduced pressure. To the residue are added ethyl acetate (10 ml) and cyclohexylamine (174 mg), and the mixture is heated with stirring at 60° C. for 18 hours. The solvent is evaporated and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (600 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084176B2
出典データセットuspto-grants-2006_08
ORD IDord-e923ca3883c74703a1879eb55299542a
出典メモuspto-grants-2006_08