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

Anticoagulant pentasaccharide compound, preparation method and medical use thereof

Active Publication Date: 2021-09-28
NANJING CHIA TAI TIANQING PHARMA
View PDF11 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the case of bleeding, it is necessary to turn off the anticoagulant effect as soon as possible, and the half-life is too long, which will increase the risk of bleeding

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
  • Anticoagulant pentasaccharide compound, preparation method and medical use thereof
  • Anticoagulant pentasaccharide compound, preparation method and medical use thereof
  • Anticoagulant pentasaccharide compound, preparation method and medical use thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0083] Preparation of compound D1: Dissolve D0 (748g) in tetrahydrofuran, use excess potassium hydroxide as a base, add dimethyl sulfate dropwise at 0°C for 2 hours, add potassium hydroxide aqueous solution to quench for 4 hours after the reaction, and then extract the fraction with ethyl acetate solution, spin-dried to obtain D1 (804g), yield 100%.

[0084] The preparation of compound D2: Add D1 (804g) to the solution of acetic acid: water: sulfuric acid = 2000g:400g:98g, add ethyl acetate and water after reflux reaction for 1h, and evaporate the organic phase to dryness to obtain D2 (690g). 89%.

[0085] Preparation of compound D3: Dissolve D2 (388g) in anhydrous dichloromethane, add 288g of trichloroacetonitrile and 15g of DBU to react for 1h, then spin to dry column chromatography to obtain D3 (490g) with a yield of 92%.

[0086] The second part preparation of monosaccharide E ring

[0087] synthetic route:

[0088]

[0089] a) dimethyl sulfate, KOH, tetrahydrofuran,...

Embodiment 1 5

[0159] Embodiment 1 pentasaccharide II-1 (R 1 for the preparation of methyl, sodium salt)

[0160] synthetic route:

[0161]

[0162] Preparation of compound DEFGH10: Dissolve DE16 (32g) and FGH5 (50g) in anhydrous dichloromethane, add TMSOTf 1g dropwise at 0°C, add triethylamine to quench after reacting for 1h, and obtain DEFGH10 (61g, Yield 81%). 1 H NMR (300MHz, CDCl 3 )δ8.05-7.55(m,5H),7.34-7.29(m,40H),5.99(d,1H),5.60(m,4H),5.17(dd,J=9.0,3.4Hz,1H),4.64 –4.62(m,18H),4.23-4.19(m,3H),4.00(m,3H),3.80-3.77(m,8H),3.70(s,6H),3.61(d,3H),3.50(d ,3H),3.41-3.40(m,18H),3.36(m,3H).MS(ESI):1815.8[M+Na] +

[0163] Preparation of compound DEFGH11: Dissolve DEFGH10 (60 g) in anhydrous methanol, add 10% palladium carbon, reduce with hydrogen under normal pressure for 24 h, filter and spin dry to obtain DEFGH11 (34 g, yield 95%). 1 H NMR (300MHz, CDCl 3 )δ8.05-7.55 (m, 5H), 5.99 (d, J = 3.6Hz, 1H), 5.60 (d, J = 8Hz, 1H), 5.40 (m, 3H), 5.17 (dd, J = 9.0, 3.4Hz, 1H), 4.77(d, 3H), 4...

Embodiment 2 5

[0166] The preparation of embodiment 2 pentasaccharide II-2 (sodium salt)

[0167] synthetic route:

[0168]

[0169] Referring to the preparation method of Example 1, DE15 and FGH5 were used as raw materials to react, and then the pentasaccharide II-2 (sodium salt) was obtained through hydrogenolysis reaction to remove benzyl group, sulfation reaction, and hydrolysis reaction.

[0170] Compound DEFGH20: 1 H NMR (300MHz, CDCl 3 )δ8.05-7.55(m,5H),7.34-7.29(m,40H),5.99(d,1H),5.97(d,J=3.4Hz,,1H),5.60(m,3H),5.17( dd,J=9.0,3.4Hz,2H),4.64–4.62(m,18H),4.23-4.19(m,4H),4.00(m,3H),3.80-3.77(m,6H),3.70(s, 6H),3.61(d,3H),3.50(d,3H),3.41-3.40(m,18H),3.36(m,2H),2.02(s,3H).MS(ESI):1843.8[M+Na ] +

[0171] Compound DEFGH21: 1 H NMR (300MHz, CDCl 3 )δ8.05-7.55 (m, 5H), 5.99 (d, J = 3.6Hz, 2H), 5.40 (m, 3H), 5.17 (dd, J = 9.0, 3.4Hz, 2H), 4.77 (d, 3H ),4.71(d,2H),4.64–4.62(m,2H),4.23-4.19(m,4H),4.10(m,1H),3.94-3.80(m,10H),3.70(d,6H), 3.57-3.50(m,8H),3.41-3.40(m,15H),3.30(m,2H),2.02...

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 relates to anticoagulant drugs, in particular to a class of synthetic pentasaccharide compounds and their salts, their preparation methods and their pharmaceutical use. The present invention synthesizes a class of ionic pentasaccharide compounds or their acids or salts as shown in II, which has stronger anticoagulant factor Xa activity and longer elimination half-life than fondaparinux sodium. The pentasaccharide compound of the present invention can be used to prepare medicines for preventing and treating diseases related to blood coagulation disorders, such as deep vein thrombosis, thrombophlebitis, arterial blockage caused by thrombosis or embolism, postoperative venous thrombosis or embolism, etc. disease.

Description

technical field [0001] The invention relates to a pentasaccharide compound used as an anticoagulant, its preparation method and its medical application in anticoagulation. Background technique [0002] Thrombotic disease is a class of diseases that seriously endanger human health, and its incidence rate ranks first among various diseases, and it has gradually increased in recent years. It is mainly divided into arterial thrombosis and venous thrombosis. Venous thrombosis is common in deep veins, clinically manifested as local pain and swelling due to thrombus formation, distal blood reflux disorder, and embolism caused by thrombus dislodgment leading to organ dysfunction. Arterial thrombosis begins with atherosclerotic lesions on the arterial wall and activation of platelets, which can lead to serious cardiovascular diseases such as acute myocardial infarction and stroke. Treatment methods include anticoagulant therapy, antiplatelet therapy, and thrombolytic therapy, and a...

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): C07H15/04C07H15/18A61K31/7028A61P7/02A61P9/10
CPCC07H15/04C07H15/18
Inventor 宋洁梅张林林吴舰赵建良王华萍徐丹朱春霞田舟山
Owner NANJING CHIA TAI TIANQING 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