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HRID 774生成日期: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/zh-CN/reaction/774

反应方程式

参与物

角色名称HCID投料
反应物N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 53886295—
催化剂HCID 178418390HCID 178418390—
溶剂(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮HCID 887—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
产物alpha-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 1179321770.1%

反应条件

温度40 °C

反应步骤

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.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05723165
来源数据集uspto-grants-1998_03
ORD IDord-1b033c485fa54b2cb55a6e97a581a99c
来源说明uspto-grants-1998_03