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

Sulfonyl pyridine amide derivatives and preparation method thereof

A technology for sulfonyl pyridine amides and derivatives, which is applied in the field of sulfonyl pyridine amide derivatives and their preparation, can solve problems such as reaction conditions restricting practicability, and achieve scientific and reasonable synthesis methods, industrialization promotion, and efficient recycling capabilities. Effect

Active Publication Date: 2020-12-29
HANGZHOU VOCATIONAL & TECHN COLLEGE
View PDF1 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the presence of noble metals and toxic transition metals, harsh reaction conditions, and high catalytic loading greatly limit the practicality of these methods

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
  • Sulfonyl pyridine amide derivatives and preparation method thereof
  • Sulfonyl pyridine amide derivatives and preparation method thereof
  • Sulfonyl pyridine amide derivatives and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0046] Preparation of Chitosan-supported Copper-Carbon Nanocatalysts

[0047] In a 100 mL round bottom flask equipped with a reflux condenser and a magnetic stir bar, anhydrous copper acetate (90.83 mg, 0.500 mmol) was dissolved in H 2 O (40mL). Chitosan (690 mg) was then added to the solution to obtain a suspension which was stirred at 50 °C for 3 h. After the solution was cooled to room temperature, the H was slowly removed by suction filtration under reduced pressure. 2 O, the filter cake was washed three times with ethanol and water to give a light blue solid. The light blue solid obtained was dried at 60° C. under vacuum for 12 hours. The dried samples were evenly transferred into porcelain boats and then put into a tube furnace. The tube furnace was evacuated and then flushed with nitrogen for half an hour. Keep nitrogen flowing in the tube furnace, heat the tube furnace to 200 °C with a temperature gradient of 2 °C / min, and keep it in nitrogen atmosphere for 2 hour...

Embodiment 1

[0049] The preparation of N-(2-ethylphenyl) pyridine-2-carboxamide (R in structural formula II 1 is pyridyl, R 2 Ortho-substituted ethyl)

[0050]In a 150mL round-bottomed flask, add 2-pyridinium formate (12mmol, 1.48g), 2-ethylaniline (10mmol, 1.21g) and 50mL of dichloromethane (DCM), stir in an ice bath, and then pour into the round-bottomed flask DCM solution mixed with dicyclohexylcarbodiimide (DCC) (15mmol, 3.1g) and 4-dimethylaminopyridine (DMAP) (5mmol, 0.61g) was added dropwise, and the reaction was continued at room temperature after the dropwise addition was completed. Hours, the reaction was checked by TLC. After the reaction is completed, the reaction solution is suction-filtered, the filtrate is collected, spin-dried, and the eluent is purified through the column with the ratio of petroleum ether and ethyl acetate (25:1), and N-(2-ethyl phenyl)pyridine-2-carboxamide.

[0051] The preparation of pyridine-3-sodium sulfinate (R in the formula III 3 for meta-subs...

Embodiment 2

[0061] The preparation of N-(2-methoxyphenyl) pyridine-2-carboxamide (R in structural formula II 1 is pyridyl, R 2 for ortho methoxy)

[0062] In a 150mL round bottom flask, add 2-pyridinium formate (12mmol, 1.48g), 2-methoxyaniline (10mmol, 1.23g) and 50mL of dichloromethane (DCM), stir under ice bath, and then pour A DCM solution mixed with dicyclohexylcarbodiimide (DCC) (15mmol, 3.1g) and 4-dimethylaminopyridine (DMAP) (5mmol, 0.61g) was added dropwise in the flask, and the reaction was continued at room temperature after the addition was complete After 6 hours, the reaction was checked by TLC. After the reaction is completed, the reaction solution is suction-filtered, the filtrate is collected, spin-dried, and the eluent is purified by column with the ratio of petroleum ether and ethyl acetate (25:1), and N-(2-methoxy phenyl)pyridine-2-carboxamide.

[0063] The preparation of N-[4-(benzenesulfonyl)-2-methoxyphenyl]pyridine-2-carboxamide (R in structural formula I 1 is...

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 relates to a Sulfonyl pyridine amide derivatives and a preparation method thereof; the preparation method comprises the following steps: adding a compound as shown in a structural formula (II), a compound as shown in a structural formula (III), an oxidant, an additive and a heterogeneous biomass supported copper catalyst into a reaction container, adding a solvent, and carrying out astirring reaction at room temperature; and after the reaction is finished, filtering, extracting, concentrating, separating and purifying to obtain the sulfonyl pyridine amide derivative with the structural formula shown in the formula (I). The synthesis method of the sulfonyl pyridine amide derivatives is scientific and reasonable, and a series of sulfonyl pyridine amide derivatives are synthesized by a green and efficient synthesis method by adopting a heterogeneous biomass copper-loaded catalyst for catalytic reaction.

Description

technical field [0001] The invention belongs to the technical field of chemical synthesis, and in particular relates to a sulfonyl pyridine amide derivative and a preparation method thereof. Background technique [0002] Arylamines are common and basic industrial raw materials, which are widely used in agriculture, materials and pharmaceutical synthesis. Sulfur-containing compounds are important components of natural products, functional materials and drugs, such as the herbicide mesotrione, the anti-migraine drugs sumatriptan and eletriptan, etc., and their structural formulas are as follows: [0003] [0004] They play an important role in biology and medicine, so it is necessary to continuously explore more efficient and concise C-S bond formation methods. [0005] Typical methods for the synthesis of sulfones include oxidation of sulfides, alkylation of sulfinates, Friedel-Crafts-type sulfonation of arenes, and electrophilic substitution of arenes with sulfonyl halid...

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 Applications(China)
IPC IPC(8): C07D213/81C07D215/48C07D217/26C07D401/12B01J31/06
CPCC07D213/81C07D215/48C07D217/26C07D401/12B01J31/06B01J2231/4294
Inventor 于文博朱军陈郁冯海霞
Owner HANGZHOU VOCATIONAL & TECHN COLLEGE
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