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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488656Generated: October 28, 2026

methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate → methyl N-{[4-(aminomethyl)cyclohexyl]carbonyl}-L-norleucinate

https://huagongshe.com/reaction/488656

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinateHCID 69803360—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productmethyl N-{[4-(aminomethyl)cyclohexyl]carbonyl}-L-norleucinateHCID 66920885—

Reaction Steps

A mixture of methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate (830 mg, 1.98 mmol), 10% palladium on C (0.056 g) in methanol (10 mL) was stirred under an atmosphere of hydrogen for 4 hours. The mixture was filtered through diatomaceous earth and the filter cake washed with methanol (2×15 mL). The combined methanol was concentrated under reduced pressure to provide the titled compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972340B2
Source datasetuspto-grants-2005_12
ORD IDord-007b4075ba5344d39cd1463e8a2d0912
Source noteuspto-grants-2005_12