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

Benzylamine compound, and its preparing method and use

A technology of benzylamine derivatives, applied in the field of new benzylamine derivatives

Active Publication Date: 2008-04-16
ZHEJIANG RES INST OF CHEM IND CO LTD +1
View PDF20 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although pyrimidine salicylates have high herbicidal activity, they are currently only suitable for weed control in cotton fields and rice fields

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
  • Benzylamine compound, and its preparing method and use
  • Benzylamine compound, and its preparing method and use
  • Benzylamine compound, and its preparing method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Synthesis of intermediate 2-methyl-3-chlorothiophenol (V):

[0056] Add 80ml of concentrated hydrochloric acid to the flask, ice bath, add 64.5g (0.4mol) of 2-methyl-3-chloroaniline under mechanical stirring, it takes about half an hour, stir for another half an hour, keep 0℃ and add 34g (0.4mol) dropwise The solution of sodium nitrite and 68ml water takes about half an hour. Stir at 0℃ for 1 hour to obtain the diazonium salt solution. Add 64g (0.4mol) potassium ethanoxanthate and 100ml water in a 1000ml flask, stir and heat to 40 -45℃, keep the temperature, drop into the above diazonium salt solution for about 2 hours, stir for 1 hour after the addition, cool, separate the lower oily substance, extract the water layer with ether, evaporate the ether, add 200mL anhydrous Ethanol, add 90 grams (1.6 mol) of potassium hydroxide in batches. The addition speed is appropriate to maintain a slight boiling. After the addition, heat to reflux for 6 hours, cool and reduce the pressur...

Embodiment 2

[0058] Preparation of Intermediate 2-(4.6-Dimethoxy-2-pyrimidinethiol)-6chlorotoluene (VI-1):

[0059] Add 15.8 grams of 2-methyl-3-chlorothiophenol (0.1 mol), 13.8 grams of anhydrous potassium carbonate (0.1 mol), 21.8 grams (0.1 mol) of 4.6-dimethoxy-2-methanesulfon to a 250 mL flask Acylpyrimidine and 200mL tetrahydrofuran, reflux for 4 hours, cool, filter with suction, wash a small amount of tetrahydrofuran, evaporate the tetrahydrofuran, add 100mL methanol, stir to precipitate a white solid, filter and dry, obtain 18.9 g, then concentrate and cool to crystallize to obtain 3.6 g, yield 76%.

Embodiment 3

[0061] Preparation of intermediate 2-(4.6-dimethoxy-2-pyrimidinyl mercapto)-6-chlorobenzyl bromide (VII-1):

[0062] Add 5.93 grams (20m mol) of 2-(3,5-dimethoxypyrimidinylmercapto)-6-chlorotoluene, 3.63 grams (20m mol) of N-bromosuccinimide, 0.3g Nitrogen diisobutyronitrile, dry CCl 4 100mL, connected to reflux condenser and drying tube, heated to reflux for 4 hours, cooled, filtered, and dissolved under reduced pressure. 15mL of methanol was added and stirred at room temperature. A white solid was precipitated, filtered and dried to obtain 5.9 g. The yield was 78.7%.

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

PropertyMeasurementUnit
diameteraaaaaaaaaa
diameteraaaaaaaaaa
Login to View More

Abstract

This invention relates to a group of benzyl amine derivatives and their preparation method, as well as their application as chemical herbicide in agriculture. In their general structural formula at right, D or E = H, halogens, C1~C4 alkyl, C1~C4 alkoxy, C1~C4 halogenated alkyl and C1~C4 halogenated alkyloxyl; R1, which can be placed on either of positions on benzene ring from 3 to 6, is = H, halogens, nitro, C1~C4 alkyl, C1~C4 alkyloxyl; R2 and R3=C1~C4 alkyl, C1~C4 halogenoalkyl, -CH2COOCH3, aryl-substituted C1~C4 alkyl, phenyl, R5-(or R6)-substituted phenyl or naphthyl and heterocyclic radical ( including pyridyl, thienyl, thiazyl and pyrimidinyl); or R2 , R3 and N combine to form circular amidogen, n= 0-2; R5 (or R6) is among H, halogens, nitro, hydroxyl, methyl, ethyl, teriarybutyl, chloromethyl, methoxyl, trifluoromethyl, trifluromethoxyl, ethoxyl, cyano and phenoxyl.

Description

Invention field [0001] The present invention relates to a new class of benzylamine derivatives, specifically 2-pyrimidine sulfoxide or sulfoxide, and sulfone benzylamine compounds, a preparation method and their use as agrochemical herbicides. Background technique [0002] Pesticides are an indispensable means of production for humans to obtain food and to ensure stable and high yields in agriculture. In the past century, pesticides such as pesticides, fungicides, and herbicides have made great contributions to mankind. In recent years, as the world’s population continues to grow, human needs for food are also increasing, but the growth rate of cultivated land is far behind the rate of population growth. To solve this worldwide problem, we must rely on increasing the amount of food per unit area. Yield and improvement of crop quality require various means, such as breeding, cultivation, fertilization, etc. The application of pesticides is also one of the indispensable means. Howe...

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): C07D239/38A01N43/54
Inventor 王国超唐庆红付群梅傅荣幸董德臻彭伟立陈杰吕龙
Owner ZHEJIANG RES INST OF CHEM IND CO LTD
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