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HRID 248323作成日:2026年10月26日

N-Methylpiperidine → N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide

https://huagongshe.com/reaction/248323

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylpiperidineHCID 12291—
反応物Isobutyl chloroformateHCID 62365—
反応物Boc-L-ValineHCID 83693—
反応物1-(4-Methoxyphenyl)ethanamineHCID 238181—
溶媒DichloromethaneHCID 6344—
生成物N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamideHCID 14774435217.1%

反応条件

温度-60 °C

反応手順

2.3 g (0.023 mol) of N-methylpiperidine are added to 5.0 g of t-butoxycarbonyl-L-valine (0.023 mol), dissolved in 50 ml of CH2Cl2, at -20° C. 3.2 g (0.023 mol) of isobutyl chloroformate are then rapidly added dropwise at -20° C., the mixture is subsequently stirred at the same temperature for 10 minutes and cooled to -60° C. and 3.5 g (0.023 mol) of 4-methoxy-1-phenylethylamine are allowed to run in, the temperature being kept below -15° C. After 2 hours at -15° C., the mixture is subsequently stirred at room temperature for 15 hours, the solid is filtered off and rinsed with CH2Cl2, the filtrate is concentrated, the residue is introduced into water, the mixture is extracted twice with ethyl acetate and the combined ethyl acetate phases are washed with NaHCO3 solution and water, dried and concentrated. 17.5 g (85% of theory) of N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide of melting point 126°-127° C. are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210084
出典データセットuspto-grants-1993_05
ORD IDord-82146073056f4aa1ba339f9fa262aa86
出典メモuspto-grants-1993_05