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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664804Generated: October 30, 2026

Benzyl 3-methyl-2-oxo-2,2',3,3'-tetrahydro-1H,1'H-spiro[1,8-naphthyridine-4,4'-pyridine]-1'-carboxylate → 3-Methyl-1H-spiro[1,8-naphthyridine-4,4'-piperidin]

https://huagongshe.com/reaction/1664804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-methyl-2-oxo-2,2',3,3'-tetrahydro-1H,1'H-spiro[1,8-naphthyridine-4,4'-pyridine]-1'-carboxylateHCID 67440213—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Methyl-1H-spiro[1,8-naphthyridine-4,4'-piperidin]HCID 86620120—

Reaction Steps

Benzyl 3-methyl-2-oxo-2,2′,3,3′-tetrahydro-1H,1′H-spiro[1,8-naphthyridine-4,4′-pyridine]-1′-carboxylate (73 mg, 0.20 mmol) was diluted in ethanol (10 mL) and palladium (10% on carbon; 100 mg) was added. The reaction vessel was evacuated and back-filled with nitrogen (3×), then back-filled with hydrogen (1 atm). After 6 h, the mixture was filtered with celite, washed with ethanol and methanol. The filtrate was concentrated to give the title compound. MS 232.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-b08268ab758448fa835e83b2334c30f1
Source noteuspto-grants-2011_10