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HRID 774作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/774

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-methoxymethylbenzylamideHCID 53886295—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物alpha-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 1179321770.1%

反応条件

温度40 °C

反応手順

To a suspension of 6.20 g (10.5 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide in 200 ml of methanol and 50 ml of water was added 1.50 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen under heat at 40° C. The catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to 15 ml. The crystal thus precipitated was removed by filtration and dried to obtain 2.69 g (7.36 mmols, 70.0% ) of α-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide.

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-1b033c485fa54b2cb55a6e97a581a99c
出典メモuspto-grants-1998_03