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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194968Generated: November 1, 2026

HCID 54313272, compound → HCID 54438115, compound

https://huagongshe.com/reaction/1194968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54313272HCID 54313272—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 54438115HCID 5443811570.6%

Reaction Steps

In 20 ml of methanol is dissolved 0.5 g of N-[N-[(S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-carboxypentyl]-L-alanyl]-N-(indan-2-yl)glycine tert-butyl ester, and a catalytic reduction is carried out at ambient temperature and under atmospheric pressure using 10% palladium-carbon (50% wet., 0.5 g) as a catalyst. After stirring at room temperature for 4 hours, the catalyst is filtered off, and the filtrate is concentrated under reduced pressure to give 0.28 g of N-[N-[(S)-5-(4-piperidyl)-1-carboxypentyl]-L-alanyl]-N-(indan-2-yl)glycine tert-butyl ester as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816466
Source datasetuspto-grants-1989_03
ORD IDord-875502f4a2804977bef596f74303ce8d
Source noteuspto-grants-1989_03