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

Preparation method of polysubstituted benzofuran derivative

A technology for benzofuran and derivatives, which is applied in the field of preparation of multi-substituted benzofuran derivatives, can solve problems such as pollution and complicated preparation methods, and achieve the effect of strong operability and simple process

Active Publication Date: 2016-06-15
北京普诺旺康医药科技有限公司
View PDF0 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Aiming at the above-mentioned technical problems in the prior art, the present invention provides a method for preparing multi-substituted benzofuran derivatives, which solves the problems in the prior art. The technical problems of complex process and serious pollution

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
  • Preparation method of polysubstituted benzofuran derivative
  • Preparation method of polysubstituted benzofuran derivative
  • Preparation method of polysubstituted benzofuran derivative

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Example 12-Phenyl-3-(phenylthio)benzofuran

[0019]

[0020] In a 25mL three-neck flask, add D-1 (220mg, 1mmol), and then add Cs 2 CO 3 (652mg, 2mmol), diphenyl disulfide (109mg, 0.5mmol), L-proline (34.5mg, 0.3mmol), cuprous iodide (19mg, 0.1mmol), phenylacetylene (102mg, 1mmol) , 5mLDMSO, under the protection of nitrogen, react in an oil bath at 90°C for 20h, add 5mL water after cooling, extract with 5mL ethyl acetate each time, after repeating four times, the extract is washed with saturated brine, anhydrous sulfuric acid After drying over sodium, the filtered liquid was distilled under reduced pressure, and the distillate was separated through a silica gel column (petroleum ether as the eluent) to obtain 248.4 mg of a yellow viscous liquid with a yield of 82%.

[0021] 1 HNMR (500MHz, CDCl 3 )δ7.67–7.58(m,2H),7.58–7.49(m,2H),7.38(t,J=7.4Hz,2H),7.35–7.27(m,5H),7.21(dd,J=12.4, 4.6Hz, 2H), 7.11(t, J=7.3Hz, 1H).

Embodiment 2

[0022] Example 22-n-Butyl-3-(phenylthio)benzofuran

[0023]

[0024] In a 25mL three-neck flask, add D-1 (220mg, 1mmol), and then add Cs 2 CO 3 (652mg, 2mmol), diphenyl disulfide (109mg, 0.5mmol), L-proline (34.5mg, 0.3mmol), cuprous iodide (19mg, 0.1mmol), 1-hexyne (82mg, 1mmol), 5mLDMSO, under the protection of nitrogen, react in an oil bath at 90°C for 20h, add 5mL water after cooling, extract with 5mL ethyl acetate each time, after repeating four times, the extract is washed with saturated brine, no After drying with sodium sulfate, the filtered liquid was distilled under reduced pressure, and the distillate was separated through a silica gel column (petroleum ether as the eluent) to obtain 203.4 mg of a yellow viscous liquid with a yield of 72%.

[0025] 1 HNMR (500MHz, CDCl 3 )δ7.61(s,1H),7.44(s,1H),7.20(s,1H),7.19-7.16(m,3H),7.09-7.01(m,3H),2.94(s,2H),1.68 (s,2H),1.37(s,2H),0.92(s,3H).

Embodiment 3

[0026] Example 32-(4-methoxyphenyl)-3-(phenylthio)benzofuran

[0027]

[0028] In a 25mL three-neck flask, D-1 (220mg, 1mmol), then add K 2 CO 3 (276mg, 2mmol), diphenyl disulfide (109mg, 0.5mmol), L-proline (34.5mg, 0.3mmol), cuprous chloride (9.9mg, 0.1mmol), p-methoxyphenylacetylene (132mg, 1mmol), 5mLDMSO, under the protection of nitrogen, react in an oil bath at 100°C for 20h, add 5mL of water after cooling, extract with 5mL of ethyl acetate each time, after repeating four times, extract the solution with saturated saline After washing, drying over anhydrous sodium sulfate, the filtered liquid was distilled under reduced pressure, and the distillate was separated through a silica gel column (petroleum ether as the eluent) to obtain 282.6 mg of a light yellow viscous liquid with a yield of 85%.

[0029] 1HNMR (500MHz, CDCl3) δ7.54–7.46(m,4H),7.36(t,J=7.5Hz,2H),7.32–7.27(m,2H),7.19(t,J=7.7Hz,2H), 7.14(s,1H),7.10(t,J=7.3Hz,1H),6.79(d,J=8.8Hz,2H),3.75(s,3H).

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 belongs to the technical field of organic chemical industry, and in particular, relates to a preparation method of a polysubstituted benzofuran derivative. The method is a coupling-tandem one-pot method, terminal alkyne, a halogenated phenol derivative and disulfide or diselenide undergo a reaction, amino acid is used as an additive, a copper salt is used as a catalyst, and under a condition of adding an alkali and in an organic solvent, a reaction is carried out to prepare the polysubstituted benzofuran derivative. An expensive palladium catalyst easily polluting the environment is not adopted, the reaction conditions are relatively mild, the process is simple, the operation is high, and the method has the prospect of industrial application.

Description

technical field [0001] The invention relates to the technical field of organic chemical industry, in particular to a preparation method of multi-substituted benzofuran derivatives. Background technique [0002] Benzofurans, an important class of heterocyclic compounds, widely exist in many biologically active compounds and natural products. They have been identified in the field of therapy as having anti-cancer, anti-tumor and immunosuppressive potentials, and are important intermediates for drug development and synthesis. Among them, 3-chalcogen-benzofuran is a very good skeleton structure, and more complex benzofuran derivatives can be prepared through 3-chalcogen-benzofuran. Therefore, it is of great significance to explore the synthesis method of 3-chalcogen-benzofuran compounds. Laroque and colleagues reported that using 2-(phenylethynyl)anisole and 4-NO 2 C 6 h 4 Synthesis of 3-chalcogen-benzofuran via electrophilic cyclization with SCl or PhSeCl. Through the cont...

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): C07D307/82
CPCC07D307/82
Inventor 刘烽张奕潘仙华
Owner 北京普诺旺康医药科技有限公司
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