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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978498Generated: October 29, 2026

1-(Piperidin-3-yl)methanamine → 7-[3-(Aminomethyl)-1-piperidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/978498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Piperidin-3-yl)methanamineHCID 90880—
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 12790859—
SolventAcetonitrileHCID 6342—
Product7-[3-(Aminomethyl)-1-piperidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 1377273991.9%

Reaction Steps

A mixture of 1.04 g (3.84 mmole) of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, 100 ml of acetonitrile and 1.32 g (11.5 mmole) of 3-aminomethylpiperidine [J. Org. Chem., 44, 4536 (1979)] were stirred at room temperature for four days. The reaction was filtered and the precipitate dissolved in aqueous ammonia, pH 10.5. The solution was filtered and the solvent removed at reduced pressure. The product was washed with water, then ether until dry to give 1.23 g of 7-[3-(aminomethyl)-1-piperidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, mp 120°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665079
Source datasetuspto-grants-1987_05
ORD IDord-8f90a4dd2e454846a956f394e8f42fad
Source noteuspto-grants-1987_05