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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198575Generated: October 31, 2026

4-(Aminomethyl)piperidine → HCID 13402008, compound

https://huagongshe.com/reaction/1198575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)piperidineHCID 23527—
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 12790859—
SolventAcetonitrileHCID 6342—
ProductHCID 13402008HCID 13402008634.5%

Reaction Steps

A mixture of 0.52 g (0.19 mmole) of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8 -naphthyridine-3-carboxylic acid, 150 mL acetonitrile, and 0.66 g (5.76 mmole) 4-aminomethylpiperidine [J. Med. Chem., 9 441 (1966)] was stirred at room temperature for four days. The reaction was filtered and the precipitate dissolved in 500 mL of aqueous ammonium hydroxide at pH 10.5. The solution was filtered and the solvent was removed at reduced pressure. The precipitate was washed with 5 mL of water, then ether until dry to give 0.42 g of 7-[4-(aminomethyl)-1-piperidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4 -oxo-1,8-naphthyridine-3-carboxylic acid, mp 203°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281612
Source datasetuspto-grants-1994_01
ORD IDord-3e56eaca3f51404ca1b6a2b87000785d
Source noteuspto-grants-1994_01