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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561171Generated: October 31, 2026

HCID 59002855, compound → HCID 59002956, compound

https://huagongshe.com/reaction/561171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59002855HCID 59002855—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 59002956HCID 5900295689%

Reaction Steps

To a suspension of ethyl 5-benzylamino-6,7-difluoro-1,4-dihydro-4-oxo-1-(2-phenylethyl)-3-quinolinecarboxylate (700 mg, 1.51 mmol) in a mixture of EtOH (2 mL) and AcOH (2 mL), was added 10% Pd—C (70.0 mg), the whole mixture was stirred at room temperature for 4 h under H2 atmosphere (1 atm). After insoluble materials were filtered off, the filtrate was concentrated in vacuo. To a solution of the residue in AcOH (2 mL), a suspension of 10% Pd—C (70 mg) in AcOH (2 mL) was added, the whole mixture was stirred at room temperature for 4 h under H2 atmosphere (1 atm). After insoluble materials were filtered off and washed with DMF, the combined filtrate and washing was concentrated in vacuo. Trituration of the residue with EtOH gave ethyl 5-amino-6,7-difluoro-1,4-dihydro-4-oxo-1-(2-phenylethyl)-3-quinolinecarboxylate (499 mg, 89%) as pale brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063221B2
Source datasetuspto-grants-2011_11
ORD IDord-7c3bc00da01349f8b2ac7afddd4273c3
Source noteuspto-grants-2011_11