7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid CAS 100361-18-

Introduction:Basic information about 7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid CAS 100361-18-, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid Basic information

Product Name:7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid
Synonyms:7-Chloro-1-Cyclopropyl-6-Fluoro-4-Oxo-1,4-Dihydro-1,8-Naphthyridin-3-Carboxylic Acid;1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyl ridine carbox.acid;7-Chloro-1-Cyclopropyl-6-Fluoro-1,4-Dihydro-4-Qxoquinoline-3-CarboxylicAcid98%;7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;7-Chloro-1-cyclopropyl-6-fluor;7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-Ox;7-Chloro-1-cyclopropyl-1,4-dihydro-3-oxo-1,8-naphthyridine-3-carboxylic aci;1-CYCLOPROPYL-6-FLUORO-1,4-DIHYDRO-4-OXO-1,8-NAPHTHYLRIDINE CARBOXYLIC ACID 99%
CAS:100361-18-0
MF:C12H8ClFN2O3
MW:282.65
EINECS:600-082-3
Product Categories:Fluorine series;Heterocycles;Intermediate;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:100361-18-0.mol

7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid Chemical Properties

Melting point 209-212 °C
Boiling point 485.9±45.0 °C(Predicted)
density 1.727±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka5.96±0.70(Predicted)
form powder to crystal
color White to Almost white
CAS DataBase Reference100361-18-0

Safety Information

HS Code 2933998090

7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid Usage And Synthesis

Chemical PropertiesOff-white or light yellow powder
UsesGemifloxacin intermediate as antibacterial agent.
Synthesis

96568-07-9

100361-18-0

Ethyl 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate (0.1 g, 0.32 mmol) was used as a raw material and dissolved in THF (5 ml). Concentrated HCl (45 μL, 0.7 mmol) was added to this solution. The reaction mixture was heated to reflux and the reaction was continued for 2 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was cooled to room temperature. The precipitated solid was collected by filtration to afford the target product 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid in a yield of 70 mg with 78% yield.

References[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 7, p. 2428 - 2433
[2] Journal of Medicinal Chemistry, 2002, vol. 45, # 25, p. 5564 - 5575
[3] Patent: WO2005/40164, 2005, A1. Location in patent: Page/Page column 10-12

7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid Preparation Products And Raw materials

Raw materials1,8-Naphthyridine-3-carboxylic acid, 1-cyclopropyl-6-fluoro-1,4,7,8-tetrahydro-4,7-dioxo--->Water-->Tetrahydrofuran-->Hydrochloric acid-->7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic Acid Ethyl Ester
7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid CAS 86393-33-1
7-CHLORO-8-METHYLQUINOLINE CAS 78941-93-2
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