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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Leucine, N-carboxy-, N-benzyl ester, L- | HCID 74840 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | L-Tyrosine 1,1-dimethylethyl ester | HCID 6950582 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57163670 | HCID 57163670 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867192B1 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-3f59995ff68d40fca1b31a5b73d632d9 |
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| Source note | uspto-grants-2005_03 |
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