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HRID 280769作成日:2026年10月25日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylester

https://huagongshe.com/reaction/280769

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Tyrosine ethyl ester hydrochlorideHCID 2724939—
反応物Dibenzylphosphory-L-alanyl-L-prolineHCID 53804723—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物dibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylesterHCID 7004048079.8%

反応条件

温度-15 °C

反応手順

Dibenzylphosphoryl-L-alanyl-L-proline (1.2 g, 2.5 m mole), HOBt (338 mg, 2.5 m mole) and L-tyrosine ethylester hydrochloride (737 mg, 3 m mole) was suspended in DMF (10 ml), and WSC (0.5 ml) was added gradually thereto while cooling to -15° C. and stirring. The reaction was carried out for 3 hours under cooling and then overnight at room temperature. To the reaction solution ethyl acetate (100 ml) was added, and the mixture was washed with 1N hydrochloric acid and water in order, and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to obtain an oily dibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylester (1.4 g). This oily material gave a single spot with Rf 0.50 by thin layer chromatography (developing solvent; chloroform:methanol:acetic acid=95:5:3, colour forming method: spraying of 25% hydrobromic acid and 0.1% ninhydrine, and heating).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04590178
出典データセットuspto-grants-1986_05
ORD IDord-d749272700094d689289500c76c638b9
出典メモuspto-grants-1986_05