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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978489Generated: October 27, 2026

7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid → 1-Ethyl-6-fluoro-7-{3-[(methylamino)methyl]pyrrolidin-1-yl}-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/978489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 12790859—
ReactantN-Methyl-1-(pyrrolidin-3-yl)methanamineHCID 13491795—
SolventAcetonitrileHCID 6342—
Product1-Ethyl-6-fluoro-7-{3-[(methylamino)methyl]pyrrolidin-1-yl}-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 48350244.4%

Reaction Steps

1.00 g (3.69 mmole) 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-napthyridine-3-carboxylic acid, 40 ml acetonitrile, and 1.27 g (11.08 mmole) N-methyl3-pyrrolidinemethanamine are stirred at room temperature for three days. The reaction was filtered and the precipitate dissolved in aqueous ammonium hydroxide at pH 11. The solution was filtered and the solvent removed at reduced pressure. The product was washed with 5 ml of water, 10 ml ethanol/ether (1:1), and finally with ether until dry to give 0.571 g of 1-ethyl-6-fluoro-1,4-dihydro-7-[3-[(methylamino)-methyl]-1-pyrrolidinyl]-4-oxo-1,8-naphthyridine-3-carboxylic acid, mp 251°-253° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665079
Source datasetuspto-grants-1987_05
ORD IDord-e00e0ffbc7164879ab0b7f4447348478
Source noteuspto-grants-1987_05