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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296219Generated: October 26, 2026

2-{[(Benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl ester → Methyl 2-amino-3-(3-[(tert-butoxycarbonyl)amino]methyl-4-methoxyphenyl)propanoate

https://huagongshe.com/reaction/1296219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-{[(Benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl esterHCID 69485806—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178418361HCID 178418361—
ProductMethyl 2-amino-3-(3-[(tert-butoxycarbonyl)amino]methyl-4-methoxyphenyl)propanoateHCID 22494331—

Reaction Steps

4.09 g of 2-{([(benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl ester was dissolved in 50 ml of methanol and 20 ml of tetrahydrofuran. 0.41 g of 10% palladium carbon was added, followed by stirring for 64 hours at room temperature in hydrogen atmosphere. The catalyst was removed by filtration and washed with ethyl acetate. The filtrate was evaporated, to give 2.92 g of (2-amino)-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)propionic acid methyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244861B2
Source datasetuspto-grants-2007_07
ORD IDord-cb97139285394dcba5763f7a514b8bbc
Source noteuspto-grants-2007_07