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HRID 770作成日:2026年10月23日

N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamide → alpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamide

https://huagongshe.com/ja/reaction/770

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-isoleucine (S)-alpha-ethylbenzylamideHCID 53679369—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物alpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 5426267272.3%

反応手順

To a suspension of 2.81 g (4.7 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide in 150 ml of methanol and 50 ml of water was added 2.0 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen at room temperature for 5 hours. The catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to be 20 ml. The crystals thus precipitated were taken out by filtration and dried to obtain 1.22 g (3.4 mmols) of α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide.

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-b4a1a9f06c874053b3ad0f85aaa15884
出典メモuspto-grants-1998_03