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

A kind of preparation 2, the method for 3-dihydroquinazoline-4 (1h)-ketone and derivatives thereof

A technology for dihydroquinazoline and derivatives, applied in chemical recovery, organic chemistry, etc., which can solve the problems of complex preparation process, difficult biodegradation, and high preparation cost, and achieve good selectivity, high utilization rate, and low loss Effect

Active Publication Date: 2017-07-14
平邑现代中药产业园有限公司
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The purpose of the present invention is to overcome the preparation of 2 in the prior art, the acidic ionic liquid catalyst that exists in 3-dihydroquinazolin-4 (1H)-ketone and derivatives thereof causes the use amount is very big because acidity is lower, preparation The cost is high, the preparation process is complicated, and it is not easy to biodegrade. However, a high-acidity ionic liquid with relatively low preparation price, easy biodegradation, small usage, more recyclable times and simplified operation process is provided as a catalyst. Method for preparing 2,3-dihydroquinazolin-4(1H)-one and derivatives thereof with mixed solution of water and ethanol as solvent

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
  • A kind of preparation 2, the method for 3-dihydroquinazoline-4 (1h)-ketone and derivatives thereof
  • A kind of preparation 2, the method for 3-dihydroquinazoline-4 (1h)-ketone and derivatives thereof
  • A kind of preparation 2, the method for 3-dihydroquinazoline-4 (1h)-ketone and derivatives thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Add 5mmol isatoic anhydride, 5mmol aniline, 5mmol benzaldehyde and 0.4mmol high acidity ionic liquid catalyst respectively to 15ml of water and ethanol mixed solution (V (water): V (ethanol) = 1:2) with stirring In a 50ml single-necked bottle, the reflux reaction time was 12min, followed by TLC (thin plate chromatography). After the reaction was completed, a large amount of solids were precipitated after cooling to room temperature. The solids were crushed, left standing, and suction filtered. 2,3-Diphenyl-2,3-dihydroquinazolin-4(1H)-one, yield 94%. The filtrate was directly added with isatoic anhydride, aniline and benzaldehyde for reuse.

[0025] 2,3-diphenyl-2,3-dihydroquinazolin-4(1H)-one: m.p.208~209℃; 1 H NMR (400MHz, DMSO-d 6 ): δ=6.27(d, J=2.4Hz, 1H, CH), 6.68(t, J=7.2Hz, 1H, ArH), 6.75(d, J=8.0Hz, 1H, ArH), 7.16(t, J=7.2Hz, 1H, ArH), 7.24~7.33(m, 8H, ArH), 7.35(d, J=7.2Hz, 2H, ArH), 7.64(d, J=2.4Hz, 1H, NH), 7.70 (d, J=8.0Hz, 1H, ArH)

Embodiment 2

[0027] Add 5mmol isatoic anhydride, 5mmol aniline, 5mmol p-methoxybenzaldehyde and 0.5mmol high acidity ionic liquid catalyst to 15ml water and ethanol mixed solution (V (water): V (ethanol) = 1:2) In a 50ml single-necked bottle with a stirrer, the reflux reaction time is 8min, TLC (thin plate chromatography) tracking detection, after the reaction is completed, a large amount of solids are precipitated when cooled to room temperature, the solids are crushed, left to stand, and suction filtered, and the resulting filter residue is vacuum After drying, pure 2-p-methoxyphenyl-3-phenyl-2,3-dihydroquinazolin-4(1H)-one was obtained in a yield of 90%. The filtrate was directly added with isatoic anhydride, aniline and p-methoxybenzaldehyde and reused.

[0028] 2-p-methoxyphenyl-3-phenyl-2,3-dihydroquinazolin-4(1H)-one: m.p.204~206℃; 1 H NMR (400MHz, DMSO-d 6 ): δ=3.64(s, 3H, OCH 3), 6.21(d, J=2.4Hz, 1H, CH), 6.69(t, J=7.6Hz, 1H, ArH), 6.76(d, J=8.0Hz, 1H, ArH), 6.88(d, J= 8.4Hz, ...

Embodiment 3

[0030] 5mmol isatoic anhydride, 5mmol p-chloroaniline, 5mmol p-tolualdehyde and 0.6mmol high acidity ionic liquid catalyst were respectively added to 25ml water and ethanol mixed solution (V (water): V (ethanol) = 1:2 ) in a 100ml single-necked bottle with a stirrer, the reflux reaction time is 20min, TLC (thin plate chromatography) tracking detection, after the reaction is completed, a large amount of solids are precipitated when cooled to room temperature, the solids are crushed, left standing, and suction filtered, the obtained filter residue Pure 2-p-chlorophenyl-3-p-methylphenyl-2,3-dihydroquinazolin-4(1H)-one was obtained after vacuum drying with a yield of 91%. Repeat use after directly adding isatoic anhydride, p-chloroaniline and p-tolualdehyde in the filtrate.

[0031] 2-p-chlorophenyl-3-p-methylphenyl-2,3-dihydroquinazolin-4(1H)-one: m.p.258~260°C; 1 H NMR (400MHz, DMSO-d 6 ): δ=2.23(s, 3H, CH 3 ), 6.24(d, J=2.4Hz, 1H, CH), 6.77(dd, J=7.6Hz, 2H, ArH), 7.11(s, 4H,...

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 method for preparing 2,3-dihydroquinazolin-4(1H)-one and its derivatives, belonging to the technical field of organic chemical synthesis. In the preparation reaction, the molar ratio of isatoic anhydride, aromatic amine and aromatic aldehyde is 1:1:1, the molar amount of high-acidity ionic liquid catalyst is 8-12% of the isatoic anhydride used, and the reflux reaction time is 4-30min , the volume of the reaction solvent water and ethanol mixture is 3 to 6 times the molar weight of isatoic anhydride, and the reaction pressure is one atmospheric pressure. After the reaction is completed, it is cooled to room temperature and filtered with suction, and the obtained filter residue is vacuum-dried to obtain pure 2,3- Dihydroquinazolin-4(1H)-one and its derivatives. Compared with the preparation methods using other catalysts, the present invention has the characteristics of less catalyst toxicity, recyclable use, better biodegradability, green and economical whole preparation process, simple and convenient operation, and convenient industrialized large-scale production.

Description

technical field [0001] The invention belongs to the technical field of organic synthesis, in particular to a method for preparing 2,3-dihydroquinazolin-4(1H)-one and derivatives thereof. Background technique [0002] 2,3-Dihydroquinazolin-4(1H)-one and its derivatives are a class of nitrogen-containing heterocyclic compounds with good biological activity and pharmacological activity. It has excellent biological activity in blood pressure, anti-rheumatic, anti-hypertensive, diuretic and other aspects, and has broad application prospects in medicine. In addition, they also have important applications in agriculture and can be used as fungicides, herbicides, etc. Therefore, the preparation of 2,3-dihydroquinazolin-4(1H)-one and its derivatives has attracted widespread attention. The traditional method for preparing 2,3-dihydroquinazolin-4(1H)-one and its derivatives is to use the "one-pot" method of three components under various catalytic systems, but this method is more or ...

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): C07D239/91
CPCY02P20/584
Inventor 沈智培卢华
Owner 平邑现代中药产业园有限公司
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