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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984749Generated: October 29, 2026

Leucine, N-carboxy-, N-benzyl ester, L- → HCID 57163670, compound

https://huagongshe.com/reaction/984749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLeucine, N-carboxy-, N-benzyl ester, L-HCID 74840—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantL-Tyrosine 1,1-dimethylethyl esterHCID 6950582—
SolventAcetonitrileHCID 6342—
ProductHCID 57163670HCID 5716367096%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of N-carbobenzyloxy-L-leucine (8.6 g) in acetonitrile (150 ml), under a nitrogen atmosphere, was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (6.83 g) and 1-hydroxybenzotriazole (4.81 g). After stirring for 30 mins at 20° C. L-tyrosine tert-butyl ester (7.7 g) was added and stirring was continued for 18 h. The mixture was concentrated in vacuo to ca. 10 ml and the residue was partitioned between 1M hydrochloric acid (300 ml) and ethyl acetate (150 ml). The layers were separated and the aqueous phase was further extracted with ethyl acetate (150 ml). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate (150 ml), water (2×150 ml) and brine (100 ml), dried over sodium sulphate and evaporated in vacuo. The residue was co-evaporated with chloroform to give the title compound as a white foam (15 g, 96%). LCMS: Rt 3.56 min; m/z 485 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867192B1
Source datasetuspto-grants-2005_03
ORD IDord-3f59995ff68d40fca1b31a5b73d632d9
Source noteuspto-grants-2005_03