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

Arylpiperazine derivative ii and its salt, preparation method and use

A technology of arylpiperazine and derivatives, which is applied in the discovery of drug lead compounds and the field of medicinal chemistry, can solve the problems of inability to cure prostate cancer, inability to improve treatment results or survival rate, etc.

Active Publication Date: 2018-10-30
广州市广金创展投资有限公司 +1
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, metastatic prostate cancer is not curable and androgen ablation therapy becomes standard therapy
None of the conventional cancer treatments for prostate cancer have been very successful, although various chemotherapeutic drugs alone or in combination with radiation therapy are used to treat patients with advanced disease
Other studies have shown that once tumor cells become hormone-resistant, standard cytotoxic agents do little to improve treatment outcomes or survival in hormone-insensitive prostate cancer, although they do provide some pain relief for patients

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
  • Arylpiperazine derivative ii and its salt, preparation method and use
  • Arylpiperazine derivative ii and its salt, preparation method and use
  • Arylpiperazine derivative ii and its salt, preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Embodiment 1: the preparation of intermediate 2

[0038]

[0039] Add 5g (0.021mol) 4-(bromoethane) phenylacetic acid, 100mL tetrahydrofuran into a 250mL round bottom flask, slowly add 21.9mL borane dimethyl sulfide complex (BMS, 2M in THF) at 0°C . The reaction mixture was reacted at 0° C. for 1 h, and then gradually returned to normal temperature. After the reaction was completed, water was slowly added to terminate the reaction, extracted with ethyl acetate (100 mL×3), the organic phases were combined, washed with water and saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude product was directly used in the next reaction without purification.

Embodiment 2

[0040] Embodiment 2: the preparation of intermediate 3

[0041]

[0042] Add 4g (18.7mmol) of intermediate 2, 3.85g (18.7mmol) of sodium saccharin, 10.32g (74.8mmol) of potassium carbonate, and 150mL of acetone into a 250mL round bottom flask, and react at 60°C for 16h. TLC showed the starting material was completely reacted. The reaction was stopped, filtered and concentrated. The crude product was purified by silica gel column chromatography, eluent: V (ethyl acetate): V (petroleum ether) = 1:6, to obtain 5.90 g of white solid, yield: 85% (using raw material 4-(bromoethane ) phenylacetic acid calculation). M.p.:97-98℃; MS(ESI,m / z):318.07[M+H] + ; 1 H NMR (500MHz, DMSO-d 6 )δin ppm: 8.33 (d, J = 7.7Hz, 1H, Ar-H), 8.15–7.98 (m, 3H, Ar-H), 7.33 (d, J = 8.0Hz, 2H, Ar-H), 7.20 (d, J=8.0Hz, 2H, Ar-H), 4.87(s, 2H, CH 2 ), 3.58 (td, J=7.0, 5.4Hz, 2H, CH 2 ),2.70(t,J=7.0Hz,2H,CH 2 ),2.23(t,J=5.2Hz,1H,OH); 13 C NMR (126MHz, DMSO-d 6 )δin ppm: 158.58, 139.19, 136.82, 135....

Embodiment 3

[0043] Embodiment 3: the preparation of intermediate 4

[0044]

[0045] In a 250 mL round bottom flask, add 4 g (12.62 mmol) of intermediate 3, 5.09 g (50.48 mmol) of triethylamine, 0.15 g of 4-(N,N-dimethyl)aminopyridine (catalytic amount), 100 mL of dichloromethane , a dichloromethane solution of 3.59 g (18.93 mmol) p-toluenesulfonyl chloride (TsCl) was slowly added at 0°C. The reaction mixture was reacted at 0° C. for 16 h, and TLC showed that the starting material was completely reacted. Slowly add water to terminate the reaction, extract with dichloromethane (100 mL×3), combine the organic phases, wash with water and saturated brine, dry over anhydrous magnesium sulfate, filter, and concentrate. The crude product was purified by silica gel column chromatography, eluent: V (ethyl acetate): V (petroleum ether) = 1:8, to obtain 4.75 g of white solid, yield: 80%. M.p.:119-120℃; MS(ESI,m / z):472.08[M+H] + ; 1 H NMR (400MHz, CDCl 3 )δin ppm: 8.33 (d, J = 7.7Hz, 1H, Ar-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 invention relates to the fields of pharmaceutical chemistry and medicament lead compound discovery, and concretely relates to arylpiperazine derivatives (1) and (2). The invention also discloses a preparation method for the novel arylpiperazine derivatives and application of the arylpiperazine derivatives to resist tumors. The compounds are subjected to preliminary pharmacodynamics research and in-vitro antineoplastic experiment, results show that the compounds show relatively good antineoplastic activity and can be used to develop and exploit novel antitumor drugs.

Description

technical field [0001] The invention relates to the field of medicinal chemistry and discovery of drug lead compounds, in particular to a class of novel arylpiperazine derivatives, their preparation method and application in antitumor drugs. Background technique [0002] Prostate cancer (PCa) is a very common disease in men, ranking second in male fatal cancers, and its morbidity and mortality are second only to lung cancer (Cancer Metast. Rev, 2005, 12, 631; CA-Cancer J . Clin, 2012.62, 10). The incidence of PCa in European and American countries is much higher than that in China, Japan and other East Asian countries, and now the incidence of prostate cancer in my country is also showing an increasing trend (Journal of Clinical Oncology, 2013, 18, 330), prostate cancer has become a global problem ( Int. J. Cancer, 1984, 33, 223). [0003] Clinically, localized disease can be cured by surgery or radiation therapy to remove or destroy cancer cells. However, metastatic prost...

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): C07D417/12A61P35/00
CPCC07D417/12
Inventor 袁牧陈洪许芳叶碧波郭洁文许冰冰梁雪邵斌豪杨宗琳黄珺珺朱柳
Owner 广州市广金创展投资有限公司
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