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

Preparation method of 1,2,3-bistriazole ligand and its application in cuaac reaction

A bistriazole and reaction technology, applied in the field of synthesis of functional structural molecules, can solve the problems of inconvenient mass synthesis, difficulty in mass synthesis, harsh reaction conditions, etc., and achieve large-scale industrial production, broad development space, and low price Effect

Active Publication Date: 2018-06-12
HENAN NORMAL UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In recent years, although compounds with one-valent copper ligands have been reported one after another, the demand for ligand research and development is far from enough for the wide application of click reactions.
In the past, for the synthesis of such ligands, the synthesis conditions often required expensive reaction raw materials, it was difficult to synthesize in large quantities, and the reaction conditions were relatively harsh.
More importantly, when synthesizing such ligands, more expensive metal ligands are often required as catalysts to promote the synthesis of target ligand compounds. The reaction conditions are uneconomical and inconvenient for large-scale synthesis.

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 1,2,3-bistriazole ligand and its application in cuaac reaction
  • Preparation method of 1,2,3-bistriazole ligand and its application in cuaac reaction
  • Preparation method of 1,2,3-bistriazole ligand and its application in cuaac reaction

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] To synthesize glycine methyl ester TMS-diyne, add glycine methyl ester hydrochloride (1.251g, 10mmol, 1equiv.), trimethylsilyl acetylene (3.27mL, 25mmol, 2.5equiv.), mass 37% aqueous formaldehyde solution (1.85mL, 25mmol, 2.5quiv.), sodium bicarbonate (0.84g, 25mmol, 1equiv.) and cuprous chloride (0.1g, 1mmol, 1equiv.), mixed and stirred at 35°C After 18 hours, the progress of the reaction was monitored by TLC. After the reaction was completed, it was extracted three times with dichloromethane / water, the organic phase was washed and dried, and separated by silica gel column chromatography to obtain 2.86 g of pure target product with a yield of 92%. The product is a colorless liquid. 1 H NMR (CDCl 3, 300 MHz, 22 °C): 3.72 (s, 3H),3.53 (s, 4H), 3.43 (s, 2H), 0.15 (s, 18H). 13 C NMR (CDCl 3 , 75 MHz, 22 °C):170.76, 100.41, 90.72, 53.25, 51.86, 43.88, -0.08.HRMS (ESI) calculated forC 15 h 28 NO 2 Si 2 ([M+H] + ) 310.1653, found 310.1647.

Embodiment 2

[0031] To synthesize glycine methyl ester diyne, add glycine methyl ester TMS-diyne (3.11g, 10mmol, 1equiv.) in 10mL tetrahydrofuran solution in a 100mL round bottom flask, and then add tetrabutylammonium fluoride (7.9g, 25mmol , 2.5equiv,), mixed and stirred at room temperature for 3 hours, the reaction process was monitored by TLC. After the reaction was completed, it was extracted three times with dichloromethane / water, and the organic phase was washed and dried, and separated by silica gel column chromatography to obtain 1.49 g of pure target product with a yield of 90%. The product is a colorless liquid. 1 H NMR (CDCl 3 , 300 MHz, 22 °C): 1 H NMR (400 MHz, CDCl 3 ) δ3.73 (s, 3H), 3.56 (s, 4H), 3.47 (s, 2H), 2.28 (s, 2H). 13 C NMR (CDCl 3 , 75MHz, 22 °C): 170.76, 100.41, 90.72, 53.25, 51.86, 43.88, -0.08. HRMS (ESI) calculated for C 9 h 11 NO 2 ([M+H] + ) 165.0790, found 165.0812.

Embodiment 3

[0033] Add 1mmol glycine methyl ester diyne, 2mmol benzyl azide, 1.2mmol N,N-diisopropylethylamine and 0.1mmol cuprous iodide into a 10mL round bottom flask, mix and stir at room temperature for 3 hours, and react The process was monitored by TLC. After the reaction was completed, it was extracted with ethyl acetate, and the organic phase was washed and separated by silica gel column chromatography to obtain the pure product of the target product. The yield was 85%. The product is a viscous liquid. 1 H NMR (400 MHz, CDCl 3 ) δ 7.38-7.28 (m, 6H), 6.85-6.79 (m,4H), 5.57 (s, 4H), 4.25 (s, 4H), 3.75 (s, 3H), 3.38 (s, 2H). 13 C NMR (101 MHz, CDCl 3 ) δ 170.8, 146.9, 134.0, 129.1, 128.6, 126.1, 123.2, 56.5, 53.3, 52.0, 50.6. HRMS (ESI) m / z calculate for (M+H + ) C 23 h 24 N 7 o 2 + 430.1986, Found: 430.1977.

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 a preparation method of 1,2,3-bis-triazole ligands and an application of the 1,2,3-bis-triazole ligands in a CuAAC reaction. With cheap and easily available glycine methyl ester hydrochloride as a base raw material, and through derivation and conversion of functional groups, a diyne compound with glycine as a structure is obtained; then under a condition of room temperature and with organic azide as a raw material and copper iodide as a catalyst, 1,2,3-bis-triazole seven-membered-ring compounds are synthesized; and with the bis-triazole compounds and derivatives thereof as substrates, a series of methods for synthesis of the 1,2,3-bis-triazole derivatives are developed. A variety of novel, highly efficient, simple and easily available ligand catalysts are provided for a click reaction, and the 1,2,3-bis-triazole ligands have obvious effect on accelerating the reaction when used as the ligands and have quite practical application.

Description

technical field [0001] The invention belongs to the technical field of synthesis of functional structure molecules, and in particular relates to a preparation method of a 1,2,3-bistriazole ligand and its application in CuAAC reaction. Background technique [0002] Since the Sharpless and Medal working groups reported in 2002 that azide and terminal alkyne can generate a five-membered triazole ring (click reaction) under the catalysis of copper, the click reaction has developed very rapidly in all aspects of biochemistry. application. In order to improve the biocompatibility of the click reaction and reduce the toxic effect of Cu(I) on living cells, two important research areas of click chemistry work today: one is the copper-free catalyzed SPAAC reaction, and the other is the ability to react with monovalent copper Ligand compounds that coordinate ions and act as facilitators. The ligand has a very good effect on reducing the toxicity of copper ions to cells while accelera...

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): C07D487/14C07H13/04C07H1/00B01J31/22C07D405/04
CPCB01J31/183B01J2231/324B01J2531/0238B01J2531/16C07D405/04C07D487/14C07H1/00C07H13/04
Inventor 李凌君尚同鹏黄申龙朱安莲
Owner HENAN NORMAL UNIV
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