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

Novel substituted thiophenepyrimidinone derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase

A hydroxyl and substituent technology, applied in the field of thienyl pyrimidone derivatives, can solve problems such as insolubility and membrane permeability difficulties

Inactive Publication Date: 2011-09-07
SOLVAY PHARMA GMBH
View PDF12 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, at least some of these compounds are rather insoluble and have difficulty with membrane permeability

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
  • Novel substituted thiophenepyrimidinone derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase
  • Novel substituted thiophenepyrimidinone derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase
  • Novel substituted thiophenepyrimidinone derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0382] In order to more fully illustrate the nature of the invention and the mode of carrying it out, the following examples are provided but should not be construed as limiting.

[0383] Preparation of the following No.1 to No.17 compounds falling within the scope of general formula (I):

[0384] Compound No.1: 3-Benzyl-5-methyl-2-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydro-3H-benzo[4,5 ]thieno[2,3-d]pyrimidin-4-one

[0385]

[0386] 2-Amino-4-methyl-4,5,6,7-tetrahydro-benzo[b]-thiophene-3-carboxylic acid ethyl ester (26.6mmol, 100mol-%) and N-benzyl-3, 4,5-Trimethoxy-benzamide (34.6 mmol, 130 mol-%) was dissolved in anhydrous 1,2-dichloroethane. Cool the reaction mixture with an ice-salt bath, add POCl 3 (1.7ml, 24.6mmol, 130mol-%). The reaction mixture was refluxed for 24 hours. Add POCl twice during reflux 3 (340 μl). The reaction mixture was poured into ice water, and after neutralization with sodium acetate, the product was extracted into dichloromethane. The ...

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

This invention relates to novel substituted thiophenepyrimidinone derivatives and their use in therapy, especially for use in the treatment and / or prevention of a steroid hormone dependent diseases or disorder, such as steroid hormone dependent diseases or disorders requiring inhibition of 17beta-hydroxysteroid dehydrogenase enzymes.

Description

field of invention [0001] The present invention relates to novel substituted compounds representing inhibitors of 17β-hydroxysteroid dehydrogenase, preferably type 1 (17β-HSD1), type 2 (17β-HSD2) or type 3 (17β-HSD3) 17β-hydroxysteroid dehydrogenase The thienopyrimidinone derivatives, their salts, pharmaceutical preparations containing these compounds and the preparation methods of these compounds. Furthermore, the present invention also relates to the therapeutic use of said benzothienone derivatives, in particular their use in the treatment or prevention of steroid hormone-dependent diseases or conditions, for example where inhibition of 17β-hydroxysteroid dehydrogenase, in particular type I 17β - HSD enzyme and / or use in steroid hormone-dependent diseases or conditions requiring regulation of endogenous 17[beta]-estradiol and / or testosterone concentrations. Background of the invention [0002] The publications and other materials used herein to illustrate the background ...

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): C07D495/04A61K31/519
CPCC07D495/04A61P15/00A61P15/08A61P17/00A61P17/02A61P17/08A61P17/10A61P17/14A61P19/10A61P25/28A61P27/12A61P29/00A61P35/00A61P43/00A61P5/24
Inventor L·希尔韦莱B·胡森J·基维尼米P·科斯克米斯P·莱赫托沃里J·梅辛格O·T·彭蒂凯宁L·比尔卡拉P·萨仑凯托H-H·索尔M·昂基拉B·J·范斯蒂恩
Owner SOLVAY PHARMA GMBH
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