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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580907Generated: October 29, 2026

4-(6-Bromo-[1,8]naphthyridin-2-yl)piperidin-1-yl-carbonyl-2-(S)-phenylsulfonylamino-beta-alanine t-butyl ester → 4-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)piperidin-1-yl-carbonyl-2-(S)-phenylsulfonylamino-beta-alanine t-butyl ester

https://huagongshe.com/reaction/580907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6-Bromo-[1,8]naphthyridin-2-yl)piperidin-1-yl-carbonyl-2-(S)-phenylsulfonylamino-beta-alanine t-butyl esterHCID 86754153—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)piperidin-1-yl-carbonyl-2-(S)-phenylsulfonylamino-beta-alanine t-butyl esterHCID 86754152—

Reaction Steps

A solution of bromide 3-6 (125 mg, 0.2021 mmol), 10% Pd/C (125 mg) and EtOH (5 ml) was stirred under 1 atm H2 for 1.0 h. The reaction mixture was then filtered through a celite pad and the filtrate concentrated to give urea 3-7 as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919792
Source datasetuspto-grants-1999_07
ORD IDord-b9ca9e98237749c89ea1a49b6822c851
Source noteuspto-grants-1999_07