Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Application of novel stable prulifloxacin mesylate in preparing anti-infectives

A drug and a new technology are applied in the application field of preparing an anti-bacterial infection drug, which can solve the problems of difficult clinical treatment of bacterial drug resistance and the like

Active Publication Date: 2012-05-30
HANGZHOU GUOGUANG PHARMA
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these antibacterial drugs cannot meet the growing and refractory diseases in recent years, namely the treatment of chronic Pseudomonas aeruginosa infection and Gram-negative bacterial infection, and with the wide application of antibacterial drugs, bacterial drug resistance The production has become a difficult problem in clinical treatment

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Application of novel stable prulifloxacin mesylate in preparing anti-infectives
  • Application of novel stable prulifloxacin mesylate in preparing anti-infectives
  • Application of novel stable prulifloxacin mesylate in preparing anti-infectives

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0062] Preparation 1: 6-fluoro-1-methyl-7-[4-(5-methyl-2-oxo-1,3-dioxol-4-yl)-methyl-1- Preparation of piperidinyl]-4-oxo-4H-[1,3]thiazetidino[3,2-a]quinoline-3-carboxylic acid

[0063] 1) Preparation of 3,4-difluoro-dithioformic acid-aniline-triethylamine salt (A):

[0064] Under nitrogen protection, put 129g (1.00mol) of difluoroaniline in a 1L reaction flask, then add 202g (2.00mol) of triethylamine, cool to 5°C, slowly add 84g (1.10mol) of carbon disulfide dropwise, and complete the addition in 5 ~10°C, stirred and reacted overnight, filtered, rinsed the filter cake with diethyl ether, and dried under vacuum at room temperature to obtain 294.2 g of light yellow solid with a yield of 96.0%. TLC developer: petroleum ether: ethyl acetate: 4:1, Rf=0.60

[0065] 2) Preparation of 3,4-difluorophenylisothiocyanate (B):

[0066] Under the protection of nitrogen, add 306g (1.00mol) of homemade A and 450mL of dichloromethane to a 1L reaction flask in sequence, stir evenly, cool t...

Embodiment 1

[0086] a. Preparation of prulifloxacin mesylate

[0087] Add 10 g of prulifloxacin prepared in Preparation Example 1 and 500 mL of acetonitrile into a 1 L three-necked flask, stir for half an hour under reflux to dissolve, then add 2.70 g of methanesulfonic acid under continuous stirring, stir for 30 minutes, add 50 mL of distilled water and 1.0 g of activated carbon , gradually warming up to reflux, and keeping warm for 2h. The reaction was almost complete, the solution became clear, filtered while it was hot, and the filtrate was refrigerated overnight, a large number of crystals were precipitated, filtered with suction, and the filter cake was washed twice with ethanol, 25 mL each time. The obtained solid was dried under reduced pressure at 40° C. for 10 h to obtain 9.74 g of off-white or light yellow solid, with a yield of 83.0%.

[0088] b. Preparation of prulifloxacin mesylate for injection

[0089] Take 50g of prulifloxacin mesylate raw material, put it in a suitable ...

Embodiment 3

[0094] Example 3: In vivo protective effect of prepared prulifloxacin mesylate on mice infected with Escherichia coli and Klebsiella pneumoniae

[0095] Taking prulifloxacin as a control, the in vivo protective effect of prulifloxacin mesylate on mice infected with Escherichia coli and Klebsiella pneumoniae was compared. In this study, Kunming mice were used as the test object, and the test strains (Escherichia coli, Klebsiella pneumoniae) were isolated from the hospital. The animals were divided into 7 groups, and the doses of the test drug given to the animals in each group were 3.5, 2.45, 1.715, 1.20, 0.84, 0.59 and 0.41 mg / kg body weight (calculated as prulifloxacin), and the mice were injected intraperitoneally with the bacterial solution for 10 minutes. Afterwards, administered by subcutaneous injection. During the test period, the mice were fed under normal conditions, and the survival of the mice within 48 hours after administration was observed.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

Prulifloxacin has low bioavailability due to poor water solubility. The invention relates to a novel prulifloxacin mesylate and a preparation thereof, a kit comprising an antibiotic preparation of the novel prulifloxacin mesylate, and application of the novel prulifloxacin mesylate in preparing an anti-bacterial infection medicine. Specifically, the invention particularly relates to a novel preparation for injection of a medicine, with a chemical name of 6-fluoro-1-methyl-7-[4-(5-methyl-2-oxo-1,3-dioxole-4-yl)-methyl-1-piperazinyl]-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-mesylate, which can be stably stored. Prulifloxacin is directly injected for administration in the form of thiabutyldine quinoline mesylate, so that the solubility, bioavailability and curative effect of prulifloxacin are improved.

Description

Technical field: [0001] The present invention relates to a new prulifloxacin mesylate and its preparation, a kit containing the pharmaceutical antibiotic preparation, and an application of the new prulifloxacin mesylate in preparing an antibacterial infection drug. Specifically, it particularly relates to a new chemical name for injection that can be stored stably: 6-fluoro-1-methyl-7-[4-(5-methyl-2-oxo-1,3-di Oxol-4-yl)-methyl-1-piperidinyl]-4-oxo-4H-[1,3]thiazetidino[3,2-a]quinoline- Pharmaceutical preparations of 3-mesylate. Background technique: [0002] Microbial infection is the main factor that threatens human health. In the process of fighting against diseases, humans have discovered a variety of antibacterial drugs: β-lactams, macrolides, aminoglycosides, other antibiotics and synthetic drugs. Synthetic drugs include the largest class of antibacterial drugs: quinolones, among which ciprofloxacin, ofloxacin, levofloxacin, pefloxacin, etc. have been widely used in c...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K31/496A61P31/04
Inventor 胡定国
Owner HANGZHOU GUOGUANG PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com