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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369796Generated: October 30, 2026

17-{3-[(2-Benzyloxycarbonylethyl)tert-butoxycarbonylamino]propionylamino}heptadecanoic acid tert-butyl ester → 17-{3-[tert-Butoxycarbonyl (2-carboxyethyl)amino]propionylamino}heptadecanoic acid tert-butyl ester

https://huagongshe.com/reaction/2369796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17-{3-[(2-Benzyloxycarbonylethyl)tert-butoxycarbonylamino]propionylamino}heptadecanoic acid tert-butyl esterHCID 68769049—
SolventTetrahydrofuranHCID 8028—
Product17-{3-[tert-Butoxycarbonyl (2-carboxyethyl)amino]propionylamino}heptadecanoic acid tert-butyl esterHCID 86647130102.6%

Reaction Steps

17-{3-[(2-Benzyloxycarbonylethyl)tert-butoxycarbonylamino]propionylamino}heptadecanoic acid tert-butyl ester (0.135 g, 0.2 mmol) was dissolved in THF (10 mL) in a flask. The flask was filled with nitrogen and purged under vacuum several times. Pd/C, wet 10% (0.03 g) was added and the flask was equipped with a balloon filled with the mixture was stirred for 16 h. The mixture was filtered through a celite, eluting with THF. The filtrate was concentrated under vacuum. TLC indicated the reaction was not complete, so the process was repeated twice more. The filtrate was concentrated under vacuum to yield a yellow oil (0.12 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710000B2
Source datasetuspto-grants-2014_04
ORD IDord-a56a7a4af1394f78af270315569bf34c
Source noteuspto-grants-2014_04