Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231179Generated: November 1, 2026

HCID 54198277, compound → L-Aspartyl-D-serine-(2,2,5-trimethylcyclopentyl)ester

https://huagongshe.com/reaction/2231179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54198277HCID 54198277—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductL-Aspartyl-D-serine-(2,2,5-trimethylcyclopentyl)esterHCID 22839474—

Reaction Steps

To a magnetically stirred solution of 0.1 mole 2,2,5-trimethylcyclopentyl-D-serinate in 100 ml dry DMF at 0° C. under an argon atmosphere is added 1 equivalent of N-Cbz-L-aspartic acid β-benzyl ester followed by addition of 1 equivalent each of Cu(II) chloride and dicyclohexylcarbodiimide. After 18 hours the mixture is poured into 200 ml 0.1N HCl and extracted with 300 ml ethyl acetate which is successively washed with saturated NaHCO3, H2O, and dried over MgSO4. Filtration and evaporation yields N-Cbz-β-benzyl-L-aspartyl-D-serine 2,2,5-trimethylcyclopentyl ester. 2 g N-Cbz-β-benzyl-L-aspartyl-D-serine 2,2,5-trimethylcyclopentyl ester in 50 ml dry CH3OH is hydrogenated in a Paar apparatus over 5% Pd/C. Upon completion of the reaction, the mixture is filtered through Celite and concentrated to dryness to yield the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04781927
Source datasetuspto-grants-1988_11
ORD IDord-c1e3003e99064f0198f6b2137074f1d1
Source noteuspto-grants-1988_11