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

4,6-dihydrofuran [3,4-d] imidazole-6- ketone derivative and salt and preparation method thereof

A technology of dihydrofuran and derivatives, applied in 4, can solve problems such as low yield, harsh reaction conditions, and subsequent separation difficulties

Inactive Publication Date: 2004-01-14
SHANGHAI INST OF PHARMA IND
View PDF0 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Japanese Patent JP (31) 27098, European Patent EP503785, CN106563A, CN1381453A, Journal of Medical Chemistry, 1996, Vol.39, No: 1323-338 have reported the preparation method of olmesartan, the method adopted When the intermediate is used to prepare an angiotensin II receptor antagonist (such as: olmesartan), there are many by-products, the reaction conditions are harsh, subsequent separation is difficult, and the yield is low

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
  • 4,6-dihydrofuran [3,4-d] imidazole-6- ketone derivative and salt and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 12

[0070] Embodiment 12-Propylimidazole-4, the preparation of 5-dicarboxylate diethyl ester:

[0071] In a 2L four-neck round bottom flask equipped with a magnetic stirrer, a thermometer, a reflux condenser, and an oil bath heating, add 80 grams of 2-propylimidazole-4,5 dicarboxylic acid, 1000 ml of absolute ethanol, and a catalytic amount of concentrated sulfuric acid. The temperature was raised to reflux, and after 16 hours of reaction, the reaction solution was concentrated to 400ml. After cooling to room temperature, the reaction solution was transferred to a 3L beaker equipped with mechanical stirring and cooled by a water bath, 400ml of ethyl acetate and 600ml of water were added, and solid sodium bicarbonate was added in batches to adjust the solution to neutral. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate 200ml×3. The combined organic layers were washed once with water, dried over magnesium sulfate, fil...

Embodiment 24

[0073] Preparation of CH 3 MgI ether solution

[0074] In a 1L four-neck round bottom flask equipped with a mechanical stirrer, a thermometer, and a reflux condenser, 18.88 grams of magnesium powder and 100 ml of ether were added, and a solution of 49 ml of methyl iodide in 49 ml of ether was added dropwise at room temperature. After the addition, reflux for 15 minutes to obtain CH 3 MgI ether solution. 2(b) Preparation of ethyl 4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylate:

[0075] In a 2L four-necked round-bottomed flask equipped with a mechanical stirrer, a thermometer, and a reflux condenser, add 40 grams of 2-propylimidazole-4,5-diethyl ether, 800 ml of ether, and stir until dissolved. Add CH dropwise 3 MgI ether solution, and completed. The reaction mixture was further stirred at room temperature for 1 hour. Add 200 ml of ethyl acetate, dropwise add 350 ml of saturated ammonium chloride solution, add 200 ml of water, separate ...

Embodiment 34

[0077] Example 34-(1-hydroxyl-1-methylethyl)-2-propylimidazole-5-carboxylic acid

[0078] In a 1L four-necked round-bottomed flask equipped with a magnetic stirrer, a thermometer, a reflux condenser, and an oil bath, add 73.35 grams of 4-(1-hydroxyl-1-methylethyl)-2-propylimidazole-5 - Ethyl carboxylate, 150 ml acetone, 367 ml 10% sodium hydroxide solution. The temperature was raised to reflux, and the reaction was carried out for 2 hours. Cool to 0°C with an ice-water bath, add concentrated hydrochloric acid to adjust the solution to neutrality, stir for 30 minutes, filter with suction, wash, and dry to obtain 33.46 g of the title compound. 1 H NMR (CDCl 3 , 400MHz): δ2.60 (2H, triplet), 1.65 (2H, sextet), 1.48 (6H, singlet), 0.86 (3H, triplet) MS (Q-Tofmicro, ESI + ): 195.10, 213.12(M+1), 235.10(M+Na), 447.21(2M+Na)

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

A 4,6-dihydrofurano[3,4-d] imidazole-6-ketone derivative, its pharmacological receptible salt, and the preparing process of said derivatives are disclosed. Said compound can be used as the intermediate for synthesizing the antagon of angiotensin II receptor.

Description

technical field [0001] The present invention relates to a series of 4,6-dihydrofuro[3,4-d]imidazol-6-one derivatives and pharmaceutically acceptable salts thereof and preparation methods of such compounds. Background technique: [0002] 4,6-dihydrofuro[3,4-d]imidazol-6-one derivatives and pharmaceutically acceptable salts thereof are a class of novel compounds, which can be used as angiotensin II receptor antagonists (such as: Olmesartan) is an important intermediate. Japanese Patent JP (31) 27098, European Patent EP503785, CN106563A, CN1381453A, Journal of Medical Chemistry, 1996, Vol.39, No: 1323-338 have reported the preparation method of olmesartan, the method adopted When the intermediate is used to prepare an angiotensin II receptor antagonist (such as: olmesartan), there are many by-products, the reaction conditions are harsh, subsequent separation is difficult, and the yield is low. Contents of the invention [0003] The technical problem to be solved in the pres...

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): C07D491/04
CPCC07D491/04
Inventor 张福利吴泰志
Owner SHANGHAI INST OF PHARMA IND
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