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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198576Generated: October 27, 2026

7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid → HCID 13772742, compound

https://huagongshe.com/reaction/1198576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 12790859—
Reactant1-(Azetidin-3-yl)-N-methylmethanamineHCID 14280898—
SolventAcetonitrileHCID 6342—
ProductHCID 13772742HCID 1377274226.9%

Reaction Conditions

Temperature5 °C

Reaction Steps

A suspension of 0.81 g (3.0 mmole) of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8 -naphthyridine-3-carboxylic acid, 0.9 g (9.0 mmole) of N-methyl-3-azetidinemethanamine and 30 mL of acetonitrile was refluxed for six hours. The reaction was cooled to 5° C. The filtered solids were washed with acetonitrile, ether, and dried in vacuo. The dried solid was suspended in 70 mL of water and made basic to pH 11.0 after filtering through a fiber glass pad to clarify, the filtrate was acidified to pH 7.4 with 1.0M hydrochloric acid. The resulting precipitate was removed by filtration, washed successively with water, 2-propanol, ether and dried in vacuo to give 270 mg of 1-ethyl-6-fluoro-1,4-dihydro-7-[3-[(methylamino)methyl]-1-azetidinyl]-4-oxo-1,8 -naphthyridine-3-carboxylic acid, mp 180°-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281612
Source datasetuspto-grants-1994_01
ORD IDord-6434b6fb1afb48d4b51b005f7fbd35d1
Source noteuspto-grants-1994_01