戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 30723作成日:2026年10月24日

Sodium Hydroxide → diethyl [4-({(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]prop-2-enoyl}amino)benzyl]phosphonate

https://huagongshe.com/ja/reaction/30723

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Thionyl ChlorideHCID 24386—
反応物DiisopropylethylamineHCID 81531—
反応物Diethyl p-aminobenzylphosphonateHCID 88358—
反応物(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acidHCID 69208981—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物diethyl [4-({(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]prop-2-enoyl}amino)benzyl]phosphonateHCID 2481121592%

反応手順

To a mixture of (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (35.0 g), acetonitrile (245 mL) and dimethylformamide (0.175 mL) was added thionyl chloride (11.4 mL) at 40-45° C. and the mixture was stirred for 1 hr. Then diethyl 4-aminobenzylphosphonate (36.3 g) was added at 5° C. and diisopropylethylamine (61.9 mL) was further added dropwise. The mixture was stirred at room temperature for 1 hr. A 1N aqueous sodium hydroxide solution (140 mL) was added to neutralize the reaction mixture and water (472.5 mL) was further added. The mixture was stirred at room temperature for 1 hr. The precipitated crystals were collected by filtration and washed with 30% acetonitrile to give diethyl [4-({(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]prop-2-enoyl}amino)benzyl]phosphonate (61.5 g, yield 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-30212eeeda4043e3a529b20fbb5fdb4d
出典メモuspto-grants-2008_09