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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868039Generated: October 28, 2026

4-(Aminomethyl)piperidine → HCID 13402008, compound

https://huagongshe.com/reaction/868039

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)] were 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-(aminomethy)-1-piperidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8naphthyridine-3-carboxylic acid, mp 203°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777175
Source datasetuspto-grants-1988_10
ORD IDord-aa400be3778e4ef6964e2d3234a14430
Source noteuspto-grants-1988_10