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

A kind of preparation method and application of whole acyl-protected 1-glucosinolate, glucose 1-thiol

A technology of glucosinolate and glucose, which is applied in the fields of medicine and sugar chemical synthesis, can solve the problems of inability to carry out the reaction, small solubility, and no effect, and achieve high reaction efficiency and yield, no irritation and odor, and mild conditions Effect

Active Publication Date: 2022-03-11
HUAZHONG UNIV OF SCI & TECH
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The inventor of the present application conjectures and confirms through experiment, why traditional one-step method uses the thioacetic acid of poisonous malodorous, and does not directly use potassium thioacetate, is because using potassium thioacetate under traditional one-step method condition can cause very low yield
This result may be due to the very small solubility of potassium thioacetate in the solvent dichloromethane at room temperature
So, is it feasible to replace the solvent with dimethylformamide, which has better solubility to potassium thioacetate, under the traditional one-step method? The experimental results show that under these conditions, the reaction cannot proceed at all, even if the reaction temperature is raised, it has no effect

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 preparation method and application of whole acyl-protected 1-glucosinolate, glucose 1-thiol
  • A kind of preparation method and application of whole acyl-protected 1-glucosinolate, glucose 1-thiol
  • A kind of preparation method and application of whole acyl-protected 1-glucosinolate, glucose 1-thiol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Weigh 1,2,3,4,6-penta-O-acetyl-D-glucose (1g, 2.6mmol) and dissolve it in ethyl acetate (15mL), add potassium thioacetate (590mg, 5.2mmol), Stir and mix, add boron trifluoride diethyl ether (1.3mL, 10.4mmol), react at a constant temperature of 50°C for 4 hours, cool the reaction solution to room temperature, add triethylamine dropwise to neutralize to pH = 7, concentrate under reduced pressure and column Chromatography yielded 987 mg of 2,3,4,6-tetra-O-acetyl-1-S-acetyl-β-D-glucose with a yield of 95%. 1 H NMR (400MHz, CDCl 3 ): δ5.29-5.24(2H,m,H-3,H-1),5.15-5.08(2H,m,H-2,H-4),4.26(1H,dd,J=12.4Hz,J =4.4Hz, H-6a), 4.09(1H, dd, J=12.4Hz, J=2.0Hz, H-6b), 3.83(1H, ddd, J=10.0Hz, J=4.4Hz, J=2.0Hz ,H-5),2.38(3H,s,SCOCH 3 ),2.07,2.03,2.02,2.00(12H,4×s,COCH 3 ).

Embodiment 2

[0045] Under traditional one-step conditions, direct use of potassium thioacetate leads to extremely low yields:

[0046] Weigh 1,2,3,4,6-penta-O-acetyl-D-glucose (1g, 2.6mmol) and dissolve it in dichloromethane (15mL), add potassium thioacetate (590mg, 5.2mmol), Stir and mix, add boron trifluoride diethyl ether (578 μL, 5.2 mmol), react at room temperature for 24 hours, dropwise add triethylamine to neutralize to pH = 7, concentrate under reduced pressure and column chromatography to obtain 2,3,4,6-tetra -O-acetyl-1-S-acetyl-β-D-glucose 312 mg, yield 30%.

Embodiment 3

[0048] Under the traditional one-step process conditions, the use of potassium thioacetate while using dimethylformamide as a solvent causes the raw materials to not react:

[0049] Weigh 1,2,3,4,6-penta-O-acetyl-D-glucose (1g, 2.6mmol) and dissolve it in dimethylformamide (15mL), add potassium thioacetate (590mg, 5.2mmol ), stirring and mixing, adding boron trifluoride diethyl ether (578 μL, 5.2 mmol), and reacting at a constant temperature of 50° C. for 4 hours, the raw materials did not react, and the yield was 0.

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 medicine and sugar chemical synthesis, and in particular relates to a preparation method and application of fully acyl-protected 1-glucosinolate and glucose 1-thiol. The preparation method is to react fully acetyl-protected glucose and potassium thioacetate in an organic solvent, catalyzed by boron trifluoride ether, and react at room temperature to 50°C for 4-8 hours to prepare fully-acetyl-protected 1-thioacetate Glucose; after the prepared all-acetyl-protected 1-thioglucose is dissolved in dimethylformamide, the thioacetyl group can be removed with hydrazine hydrate to obtain the full-acetyl-protected glucose 1-thiol; Glucose 1-thiol can be further used to prepare auranofin and ggliflozin thioglycoside analogues. The method of the invention has mild reaction conditions, easy operation, low synthesis cost, relatively green, and high yield. Auranofin is a medicine for treating rheumatoid arthritis, and ggliflozin thioglycoside analogues are potential medicines for treating type 2 diabetes. drug.

Description

technical field [0001] The invention belongs to the technical field of medicine and sugar chemical synthesis, and in particular relates to a preparation method and application of fully acyl-protected 1-thioglucose and glucose 1-thiol. Background technique [0002] Auranofin is an oral drug that has been on the market for many years and can be used to treat rheumatoid arthritis. Recent studies have shown that it also has anti-inflammatory and potential anti-tumor activities. It is usually prepared from peracetyl-protected glucose 1-thiol, triethylphosphine and potassium chloroaurate. Gliflozin drugs are drugs developed from bark bark glycosides (phlorizin) for the treatment of type 2 diabetes. They are both inhibitors of the glucose cotransporter (SGLT-2), as follows: [0003] [0004] Ggliflozin SGLT-2 Inhibitors [0005] Since bark glycoside is an oxygen glycoside, it is easily hydrolyzed by β-glucosidase, so it cannot be used as a drug. Ggliflozin drugs are all car...

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): C07H15/26C07H15/203C07H1/00C07H23/00A61P19/02A61P29/00A61P3/10C07H13/04
CPCC07H15/26C07H15/203C07H1/00C07H23/00A61P19/02A61P29/00A61P3/10C07H13/04
Inventor 董海冯广京
Owner HUAZHONG UNIV OF SCI & TECH
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