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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417238Generated: November 3, 2026

N-Methylpiperidine → HCID 12982235, compound

https://huagongshe.com/reaction/2417238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
Reactant5-amino-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 11023362—
ReactantHCID 11075684HCID 11075684—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 12982235HCID 12982235—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture consisting of 5-amino-6,7-difluoro-1-[(1R,2S)-2-fluoro-1-cyclopropyl]-1,4-dihydro-8-methyl-4-oxoquinoline-3-carboxylic acid (45 mg, 0.144 mmol), (3S,4R)-4-(1-tert-butoxycarbonylaminocyclopropyl)-3-fluoropyrrolidine (52.8 mg, 0.216 mmol), 1-methylpiperidine (18.5 mg, 0.186 mmol) and dimethyl sulfoxide (1.8 ml) was stirred at an outer temperature of 80° C. for 7 hours. When analysis was carried out by a high performance liquid chromatography after completion of the reaction, formed ratio of the compound of interest 5-amino-7-[(3S,4R)-4-(1-tert-butoxycarbonylaminocyclopropyl)-3-fluoropyrrolidinyl]-6-fluoro-1-[(1R,2S)-2-fluoro-1-cyclopropyl]-1,4-dihydro-8-methyl-4-oxoquinoline-3-carboxylic acid was 4%. Also, residual ratio of the starting material was 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825353B2
Source datasetuspto-grants-2004_11
ORD IDord-d633c4fdb8a444ce9a25e72a82f8a7d8
Source noteuspto-grants-2004_11