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HRID 776作成日:2026年10月23日

N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamide → alpha-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamide

https://huagongshe.com/ja/reaction/776

反応式

関与物質

役割名称HCID仕込み量
反応物N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamideHCID 54314208—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物alpha-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamideHCID 5421338550.3%

反応条件

温度40 °C

反応手順

To a suspension of 1.20 g (1.99 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide in 50 ml of methanol and 10 ml of water was added 0.30 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen under heat at 40°C., 40 ml of water was added thereto, the catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to 5 ml. The crystal thus precipitated was removed by filtration and dried to obtain 0.38 g (1.00 mmol, 50.3%) of α-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723165
出典データセットuspto-grants-1998_03
ORD IDord-29bd294101a04d54b49813c6be393808
出典メモuspto-grants-1998_03