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

A kind of ofloxacin (rhodanine unsaturated ketone) amide derivative and its preparation method and application

A technology of amide derivatives, ofloxacin, used in drug combination, organic chemistry, antitumor drugs, etc.

Active Publication Date: 2016-05-18
JIANGSU SHAXING CHEM
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the molecular structure construction between the fluoroquinolone skeleton and the rhodanine skeleton has not been reported yet.

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
  • A kind of ofloxacin (rhodanine unsaturated ketone) amide derivative and its preparation method and application
  • A kind of ofloxacin (rhodanine unsaturated ketone) amide derivative and its preparation method and application
  • A kind of ofloxacin (rhodanine unsaturated ketone) amide derivative and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Ofloxacin (5-benzylidene-rhodanine-3-yl)-amide (I-1), its chemical structural formula is:

[0046]

[0047] That is, Ar in formula I is phenyl.

[0048] The preparation method of this compound is: get ofloxacin (rhodanine-3-base)-amide (IV) 1.0g (2.0mmol) and anhydrous sodium acetate 0.20g (2.4mmol) are dissolved in 15mL glacial acetic acid, 0.25 g (2.4 mmol) of benzaldehyde was added, and the mixed reactant was refluxed for 12 h. The solvent was distilled off under reduced pressure, the residue was dissolved in water (20 mL), and 0.1 g of activated carbon was added to decolorize at 60° C. for 0.5 h, and filtered. The filtrate was basified with concentrated ammonia water to pH 9.0, extracted with chloroform (3×15 mL), and the combined organic phases were dried over anhydrous sodium sulfate. The solvent was recovered under reduced pressure to dryness, and recrystallized from ethanol-DMF (V:V=5:1) to obtain a light yellow crystal (I-1), with a yield of 72.8%, m.p.193...

Embodiment 2

[0050] Ofloxacin (5-p-methoxybenzyl-rhodanine-3-yl)-amide (I-2), its chemical structural formula is:

[0051]

[0052] That is, Ar in formula I is p-methoxyphenyl.

[0053] The preparation method of this compound is: get ofloxacin (rhodanine-3-base)-amide (IV) 1.0g (2.0mmol) and anhydrous sodium acetate 0.20g (2.4mmol) are dissolved in 15mL glacial acetic acid, 0.30 g (2.2 mmol) of p-methoxybenzaldehyde was added, and the mixed reactant was refluxed for 12 h. The solvent was distilled off under reduced pressure, the residue was dissolved in water (20 mL), and 0.1 g of activated carbon was added to decolorize at 60° C. for 0.5 h, and filtered. The filtrate was basified with concentrated ammonia water to pH 9.0, extracted with chloroform (3×15 mL), and the combined organic phases were dried over anhydrous sodium sulfate. The solvent was recovered under reduced pressure to dryness, and recrystallized from ethanol-DMF (V:V=5:1) to obtain a light yellow crystal (I-2), with a y...

Embodiment 3

[0055] Ofloxacin (5-o-methoxybenzyl-rhodanine-3-yl) amide (I-3), its chemical structural formula is:

[0056]

[0057] That is, Ar in formula I is o-methoxyphenyl.

[0058] The preparation method of this compound is: get ofloxacin (rhodanine-3-base) amide (IV) 1.0g (2.0mmol) and anhydrous sodium acetate 0.20g (2.4mmol) and dissolve in 15mL glacial acetic acid, add 0.30 g (2.2 mmol) of o-methoxybenzaldehyde, and the mixed reactants were refluxed for 12 hours. The solvent was distilled off under reduced pressure, the residue was dissolved in water (20 mL), and 0.1 g of activated carbon was added to decolorize at 60° C. for 0.5 h, and filtered. The filtrate was basified with concentrated ammonia water to pH 9.0, extracted with chloroform (3×15 mL), and the combined organic phases were dried over anhydrous sodium sulfate. The solvent was recovered under reduced pressure to dryness, and recrystallized from ethanol-DMF (V:V=5:1) to obtain a light yellow crystal (I-3), with a yi...

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

The invention discloses an ofloxacin (rhodanine unsaturated ketone) amide derivative and a preparation method and an application thereof. The ofloxacin (rhodanine unsaturated ketone) amide derivative adopts the following chemical structural general formula I (shown in the specification); and in the formula I, Ar represents a benzene ring or a substituted benzene ring or a furan ring or a pyridine ring. On the basis of a medicine molecule construction strategy of pharmacophore splice, the ofloxacin (rhodanine unsaturated ketone) amide derivative disclosed by the invention implements superposition of four pharmacophores of a chiral tricyclic fluoroquinolone skeleton, amide, rhodanine and alpha, beta-unsaturated ketone, so that the antineoplastic activity of a new compound is improved, and the toxic or side effects on normal cells are reduced, and the ofloxacin (rhodanine unsaturated ketone) amide derivative can be used as an antineoplastic active substance for developing an antineoplastic medicament of a brand-new structure.

Description

technical field [0001] The invention belongs to the technical field of innovative drug synthesis, and specifically relates to a kind of ofloxacin (rhodanine unsaturated ketone) amide derivative, and also relates to the preparation of ofloxacin (rhodanine unsaturated ketone) amide derivative The preparation method and its application in the preparation of antitumor drugs. Background technique [0002] New drug innovation originates from the discovery of lead substances, and rational drug design based on structure or mechanism is an effective method to discover lead substances. Antibacterial fluoroquinolones are based on 1-substituted-6-fluoro-quinoline (naphthyridine)-4-one-3-carboxylic acid as the dominant skeleton, and its target is topoisomerase (Topo). Functionally, it is similar to the corresponding Topo in mammalian cells, and this enzyme is also an important target of anti-tumor drugs. Therefore, structural modification of existing fluoroquinolone drugs can convert t...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C07D498/06A61P35/00A61P35/02
CPCC07D498/06
Inventor 刘彬王蕊付建民闫强吴书敏倪礼礼胡国强
Owner JIANGSU SHAXING CHEM
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