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

Synthesis method of alogliptin benzoate

A synthesis method and technology of benzoic acid, applied in carboxylate salt preparation, organic chemistry, etc., can solve the problems that impurity content is difficult to meet the qualified requirements of raw materials, resulting in reduced yield, high anhydrous requirements, etc., to achieve industrial production and easy Control, less environmental pollution effect

Active Publication Date: 2014-12-10
JIANGSU DEYUAN PHARMA
View PDF3 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Its main disadvantages are: sodium hydride is used, and the anhydrous requirement of the reagent is relatively high; methyl iodide is used, which is highly toxic; and by-products will be generated in the first step , difficult to remove in subsequent steps, and will further generate other by-products
The disadvantage of this scheme is that the solvent used in the second step is n-butanol, the reaction temperature is too high, resulting in a decrease in yield, and the impurity content in the product is difficult to meet the qualified requirements of the raw material drug

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
  • Synthesis method of alogliptin benzoate
  • Synthesis method of alogliptin benzoate
  • Synthesis method of alogliptin benzoate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] Embodiment 1, a kind of synthetic method of alogliptin benzoate comprises the following steps:

[0043] (1) 2-Cyanobenzyl bromide and 3-methyl-6-chlorouracil were stirred and reacted in toluene in the presence of tri-n-butylamine, cooled and added with water to stir and crystallize, filtered and washed to obtain 2-(6-chloro- 3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-benzonitrile;

[0044] (2) 2-(6-Chloro-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-benzonitrile and (R)-3- Aminopiperidine dihydrochloride and alkali were added to ethanol, stirred and reacted, and after purification, it was salified with benzoic acid to obtain 2-({6-[(3R)-3-aminopiperidin-1-yl]-3- Methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl}methyl)-benzonitrile monobenzoate.

Embodiment 2

[0045] Example 2, in the step (2) of the synthetic method of alogliptin benzoate described in Example 1, the amount of the substance used (R)-3-aminopiperidine dihydrochloride is 2-( 1.0 to 1.5 times the amount of 6-chloro-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-benzonitrile.

Embodiment 3

[0046] Example 3, in the step (2) of the synthesis method of alogliptin benzoate described in Example 1 or 2, the base is sodium bicarbonate or sodium carbonate.

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 discloses a synthesis method of alogliptin benzoate. The synthesis method comprises the following steps: putting 2-cyano benzyl bromide, 3-3metyl-6-chlorouracil and tri-n-butylamine in methylbenzene and stirring for reaction; cooling, adding water and stirring for crystallization; filtering and washing with water to obtain 2-(6-chlorine-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimdine-1-metyl)-benzonitrile; adding 2-(6-chlorine-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimdine-1-metyl)-benzonitrile, (R)-3-piperidinamine dihydrochloride and alkali into ethyl alcohol and stirring for reaction; purifying and salifying with benzoic acid to obtain alogliptin benzoate. The synthesis method disclosed by the invention is mild in condition, easy to control, non-toxic, environment-friendly, high in purity and high in yield.

Description

technical field [0001] The invention belongs to the technical field of medicinal chemistry, and in particular relates to alogliptin benzoate: 2-({6-[(3R)-3-aminopiperidin-1-yl]-3-methyl Synthetic method of base-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl}methyl)-benzonitrile monobenzoate. Background technique [0002] Dipeptidyl peptidase IV (DPP4) is a type II membrane protein, a nonclassical serine amino dipeptidase. It is constitutively expressed on epithelial and endothelial cells of a variety of different tissues (gut, liver, lung, kidney and placenta) and is also found in body fluids. DPP4 is also expressed on circulating T-lymphocytes and has been shown to be synonymous with the cell surface antigen CD-26. [0003] According to the introduction of Chinese published patent document CN 101309689, DPP4 is the cause of GLP-1 (7-36) (glucagon) metabolic cracking in vivo, and it has been proved that many other peptides (CHRH, NPY, GLP- 2. VIP) has proteolytic activity. GLP...

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
IPC IPC(8): C07D401/04C07C51/41C07C63/08
CPCC07D401/04
Inventor 郑家通杨汉跃董超陈学民朱思梅
Owner JIANGSU DEYUAN 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