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

Imide derivatives ar Salts thereof

A technology of amide derivatives and salts, which is applied in the field of amide derivatives or their salts and therapeutic agents for treating diabetes, and can solve problems such as not indicating insulin secretion and enhancing insulin sensitivity

Inactive Publication Date: 2004-01-28
ASTELLAS PHARMA INC
View PDF3 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the patent does not indicate that these compounds have the effect of promoting insulin secretion and enhancing insulin sensitivity

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
  • Imide derivatives ar Salts thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0080] Add 4N hydrogen chloride-ethyl acetate solution (10ml) to 458mg of (R)-N-(2-hydroxy-2-phenylethyl)-N-[2-[4-[(2-pyridinecarbonyl)amino]benzene base] ethyl] tert-butyl carbamate in 10 ml ethanol solution. The reaction solution was stirred at room temperature for 3 hours, then the solvent was evaporated under vacuum. The obtained crude crystals were recrystallized from methanol-ethanol-ethyl acetate to obtain 289 mg of (R)-4'-[2-[(2-hydroxy-2-phenylethyl)amino]ethyl]-2-pyridine Carboxanilide Hydrogen Chloride.

Embodiment 2

[0083] (R)-2-[1-(4-chlorobenzyl)-1H-imidazol-2-yl]-4'-[2-[(2-hydroxyl-2-phenylethyl)amino]ethyl] Acetanilide Hydrogen Chloride

Embodiment 3

[0085] (R)-2-[1-(3,4-dichlorobenzyl)-1H-tetrazol-5-yl]-4'-[2-[(2-hydroxyl-2-phenylethyl)amino ]ethyl]acetanilide hydrochloride

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

An amide derivative represented by the following formula: wherein the ring B is a heteroaryl group; X is a bond or a lower alkylene group; and R is a hydrogen atom, a halogen atom, a lower alkyl group, an amino group, an aryl lower alkyl group or a haloaryl lower alkyl group, or a salt thereof, is disclosed. A therapeutic agent for diabetes mellitus having both an insulin secretion promoting action and an insulin sensitivity potentiating action and also having anti-obesity and anti-hyperlipemia actions due to a selective stimulating action to beta3-receptors, is also disclosed.

Description

technical field [0001] The present invention relates to a class of medicines, more specifically to novel amide derivatives or their salts and therapeutic agents for treating diabetes. Background technique [0002] Diabetes mellitus, a disease accompanied by symptoms of persistent hyperglycemia, is now thought to be due to a number of environmental and genetic factors. The main control factor of blood sugar is insulin, and it has been recognized that hyperglycemia is caused by a lack of insulin or an excess of factors that inhibit insulin response (such as genetic reasons, lack of exercise, obesity and stress). [0003] There are two main types of diabetes. One is insulin-dependent diabetes mellitus (IDDM) caused by autoimmune diseases that reduce the function of pancreas to secrete insulin, and the other is non-insulin-dependent diabetes mellitus (IDDM) that is caused by the fatigue of continuous high-level secretion of insulin by the pancreas, which reduces the function of...

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): C07C233/07A61K31/16A61P3/10C07C229/38C07C233/65C07D213/30C07D213/56C07D213/81C07D215/48C07D231/12C07D233/26C07D233/64C07D235/16C07D235/30C07D239/26C07D241/12C07D257/04C07D277/36C07D277/40C07D277/82C07D401/04C07D513/04
CPCC07D231/12C07D213/30C07D213/56C07D233/26C07D235/30C07D277/82C07D513/04C07D241/12C07D257/04C07D215/48C07D235/16C07D277/36C07D213/81C07D239/26C07D401/04A61P3/10A61P3/04A61P3/06A61P43/00C07D213/24
Inventor 丸山龙也铃木贵之恩田健一早川昌彦森友博幸君塚哲也松井哲夫
Owner ASTELLAS PHARMA INC
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