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HRID 15014作成日:2026年10月25日

p-Toluenesulfonic acid → 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol

https://huagongshe.com/reaction/15014

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物ChloroformHCID 6212—
反応物1-(2-Chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dioneHCID 16090339—
反応物Acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl esterHCID 59341182—
溶媒2-Methylphenethyl alcoholHCID 88267—
生成物2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanolHCID 5934120032.6%

反応条件

温度100 °C

反応手順

To a solution of 0.2 gm of acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester (0.8 mmol) in 3 mL of 5:1 toluene-ethanol was added 0.20 gm of 1-(2-chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione and 10 mg of p-TsOH. The reaction mixture stirred at 100° C. for 72 h. The reaction mixture was poured into 200 mL of CHCl3 and washed twice with water (100 mL), saturated brine, dried (Na2SO4), and the solvents removed under reduced pressure. The residue was purified by column chromatography using 4% methanol-chloroform as an eluent to give 100 mg (25% yield) of an oil. This was used without further purification or characterization.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732457B2
出典データセットuspto-grants-2010_06
ORD IDord-54e07e9af4464f6988cfab1ed5303406
出典メモuspto-grants-2010_06