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

A class of biarylpyridine deubiquitinase inhibitors, its preparation method and application

A pyridyl and halogen technology, applied in organic chemistry, pharmaceutical formulation, bulk chemical production, etc., can solve the problems of unsatisfactory micromolar level specificity and low efficiency, and achieve reasonable route design, simple operation and high yield Effect

Active Publication Date: 2021-09-03
杭州市西溪医院
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] DUBs as an anti-tumor drug target is a current research hotspot, but the inhibitors targeting DUBs have low efficacy and the IC of most inhibitors 50 At the micromolar level and unsatisfactory specificity, there is currently no highly specific DUBs inhibitor that has been officially approved for marketing in clinical practice

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 class of biarylpyridine deubiquitinase inhibitors, its preparation method and application
  • A class of biarylpyridine deubiquitinase inhibitors, its preparation method and application
  • A class of biarylpyridine deubiquitinase inhibitors, its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0103] Example 1 3-bromo-5-(4-methoxybenzylthio)pyridine

[0104]

[0105] 4-Methoxybenzylthiol (32.55g, 211.07mmol) was dissolved in 500mL dimethylformamide, NaH (9.29g, 232.18mmol) was added, and reacted at 20°C for 30min, then, 3,5-dibromopyridine ( 1,50.00g, 211.07mmol), react at 20°C for 16 hours, add 100mL of water to terminate the reaction, extract with ethyl acetate (100mL x 3), wash the organic layer with water (200mL x 3), dry over anhydrous sodium sulfate, and recover under reduced pressure The solvent was separated by column chromatography to obtain 48.0 g of white solid (compound 2), with a yield of 73%. 1 HNMR (400MHz, CDCl 3 ): δ=8.38(d, J=2.1Hz, 1H), 8.31(d, J=1.9Hz, 1H), 7.60(t, J=2.0Hz, 1H), 7.13-7.08(m, 2H, Ar- H),6.79-6.73(m,2H,Ar-H),4.00(s,2H,CH 2 ),3.71(s,3H,CH 3 ).ESI-MS: m / z=311[M+H] + .

Embodiment 2

[0106] Example 2 3-(2-isopropylphenyl)-5-(4-methoxybenzylthio)pyridine

[0107]

[0108] Compound 2 (15.00g, 48.35mmol), 2-isopropylphenylboronic acid (8.72g, 53.19mmol), Pd(dppf)Cl 2 (3.54g, 4.84mmol) and sodium carbonate (10.25g, 96.71mmol) were added to 150mL of dioxane / water (10 / 1), stirred and reacted at 100°C for 16 hours, and the solvent was recovered under reduced pressure after the reaction, and 20mL of water was added , extracted with dichloromethane (50mL x 3), dried over anhydrous sodium sulfate, recovered the solvent under reduced pressure, and obtained 13.6g of yellow oil (compound 3) by column chromatography with a yield of 78%. 1 H NMR (400MHz, CDCl 3 ): δ=8.52(d, J=2.2Hz, 1H, pyridine-H), 8.36(d, J=1.9Hz, 1H, pyridine-H), 7.48(t, J=2.1Hz, 1H, pyridine-H ),7.42-7.35(m,2H,Ar-H),7.25-7.16(m,2H,Ar-H),7.11-7.02(m,1H,Ar-H),6.81(d,J=8.6Hz, 2H,Ar-H),4.10(s,2H,CH 2 ),3.78(s,3H,CH 3 ),2.86(q,J=13.7,6.8Hz,1H,CH),1.15(t,J=10.8Hz,6H,CH 3 ).ESI-MS: m / z=359.5[M+H] ...

Embodiment 3

[0109] Example 3 3-benzyl-5-(4-methoxybenzylthio)pyridine

[0110]

[0111] Synthesis of Compound 4: Using Compound 2 and 2-ethylphenylboronic acid as raw materials, the synthesis and post-treatment were the same as in Example 2. 11.7 g of a yellow oil (compound 4) was obtained, yield 72%. 1 H NMR (400MHz, CDCl 3): δ=8.52(d, J=2.1Hz, 1H, pyridine-H), 8.38(d, J=1.8Hz, 1H, pyridine-H), 7.50(t, J=2.0Hz, 1H, pyridine-H ),7.39–7.15(m,5H,Ar-H),7.10(d,J=7.7Hz,1H,Ar-H),6.81(d,J=8.6Hz,2H,Ar-H),4.11(d ,J=7.4Hz,2H,CH2),3.78(s,3H,CH3),2.50(q,J=7.5Hz,2H,CH2),1.07(t,J=7.5Hz,3H,CH3).ESI- MS:m / z=336.5[M+H] + .

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 present invention designs and synthesizes a class of biarylpyridine deubiquitinase inhibitors, which have the structure of general formula (I): Formula (I) The biarylpyridine deubiquitinase inhibitors provided by the present invention have Sutinase has good inhibitory activity, and has good in vitro proliferation inhibitory effect on tumor cells such as K562 cells, Hep‑G2 cells, HCT‑116 cells, WSD‑DLCL2 cells and A549 cells. The raw materials required for the synthesis of the compound of the invention are easily available, the route design is reasonable, the reaction conditions are mild, the yield of each step is high, the operation is simple and convenient, and the method is suitable for industrial production.

Description

technical field [0001] The invention relates to the field of medicine, in particular, the invention relates to a new class of biarylpyridine deubiquitinase inhibitors, its preparation method and application, and the application of the compound in the preparation of antitumor drugs. Background technique [0002] Malignant tumor is one of the major diseases that seriously endanger human health. The prevention and treatment of tumors has become a subject of widespread attention worldwide, and the research and development of antitumor drugs is also in an extremely urgent need. The morbidity and mortality of various tumors continue to rise, and the treatment of tumors is facing great challenges (CA-Cancer.J.Clin.2016,66,115-132). The high morbidity and mortality of tumors also provides a broad market space for tumor therapeutic drugs. In 2014, the global anti-tumor drug market has reached 60 billion US dollars. Therefore, it is imminent to find new drug targets for tumor treatm...

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): C07D213/70C07D417/12C07D333/42C07D333/44C07D409/12C07D417/14C07D409/14C07D405/14C07D401/14C07D413/12C07D405/06C07D413/14A61K31/44A61K31/4439A61K31/381A61K31/4436A61K31/4545A61K31/444A61K31/495A61K31/496A61K31/443A61K31/454A61P35/00A61P35/02
CPCC07D213/70C07D333/42C07D333/44C07D401/14C07D405/06C07D405/14C07D409/12C07D409/14C07D413/12C07D413/14C07D417/12C07D417/14Y02P20/55
Inventor 蔡兆斌张建康席建军邵益丹潘旭旺赵艳梅何若愚刘寿荣茅维嘉方红英俞哲黄斌朱元东柯云玲史婷婷琚立萍庄让笑
Owner 杭州市西溪医院
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