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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638691Generated: November 3, 2026

HCID 19841134, compound → HCID 19841155, compound

https://huagongshe.com/reaction/1638691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19841134HCID 19841134—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 19841155HCID 1984115532.4%

Reaction Steps

To 1-cyclopropyl-7-(4-benzyl-1-piperazinyl)-6-fluoro-8-hydroxymethyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (132 mg) are added 10% Pd-C (68 mg) and ethanol (10 ml), and the mixture is subjected to catalytic reduction under hydrogen gas atmosphere at 60° C. for 6.5 hours. After filtering off the catalyst, the filtrate is concentrated. The resulting residue is recrystallized from ethanol-acetone-dichloromethane to give 1-cyclopropyl-7-(1-piperazinyl)-6-fluoro-8-hydroxymethyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (34.2 mg), as white powder, m.p. 149°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880806
Source datasetuspto-grants-1989_11
ORD IDord-22529f3fa8c94bb1a26bdb83a1d74f71
Source noteuspto-grants-1989_11