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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385579Generated: October 30, 2026

HCID 57815315, compound → HCID 57815387, compound

https://huagongshe.com/reaction/385579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57815315HCID 57815315—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 57815387HCID 5781538759.7%

Reaction Conditions

Temperature47.5 °C

Reaction Steps

To a solution of 0.30 g of tert-butyl ((7-oxo-7,8-dihydro-1,8-naphthyridin-2-yl)methyl)(1-(trifluoroacetyl)piperidin-4-yl)carbamate in 40 mL of methanol, 0.10 g of 10% palladium-carbon was added, and the mixture was stirred at 45 to 50° C. for 9 hours 30 minutes under a hydrogen atmosphere. The reaction mixture was cooled to room temperature, the insoluble substance was filtered off, and the filtration residue was washed with methanol. The solvent was distilled off under reduced pressure, and the resultant residue was purified by silica gel column chromatography using an eluent of chloroform:methanol=100:3 to obtain 0.18 g of tert-butyl ((7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)methyl)(1-(trifluoroacetyl)piperidin-4-yl)carbamate as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-21e6899c73ae448eaf10f0ae1dccd495
Source noteuspto-grants-2013_02