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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843720Generated: October 31, 2026

HCID 54105171, compound → HCID 53986216, compound

https://huagongshe.com/reaction/843720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54105171HCID 54105171—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 53986216HCID 5398621680.8%

Reaction Steps

A mixture of N-(3-pyridyl)-3(R)-(tert-butoxycarbonylamino)succinamic acid ethyl ester (0.62 g) and PtO2 (0.06 g) in acetic acid (12 ml) was hydrogenated. at atmospheric pressure for 6 hours. After the catalyst was removed by filtration, the filtrate was concentrated in vacuo. The residue was dissolved in water. The solution was adjusted to pH 10 with saturated aqueous potassium carbonate solution, and extracted with ethyl acetate. The extract was washed with water and brine, and dried over MgSO4, and evaporated in vacuo to give N-(3-piperidyl)-3(R)-(tert-butoxycarbonylamino)succinamic acid ethyl ester (0.51 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380215B1
Source datasetuspto-grants-2002_04
ORD IDord-6e14fb2e45ac4e6dbd9943ada48016fa
Source noteuspto-grants-2002_04