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

Carboxylic acid derivative substituted imino aryl compound as well as preparation method, weeding composition and application thereof

A technology of carboxylic acid derivatives and imino groups, which is applied in the field of pesticides and can solve the problem of unsatisfactory crop selectivity in the herbicidal performance of harmful plants

Active Publication Date: 2021-07-13
QINGDAO KINGAGROOT CHEM COMPOUNDS CO LTD
View PDF14 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the herbicidal properties of these known compounds against harmful plants and the selectivity to crops are not entirely satisfactory

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
  • Carboxylic acid derivative substituted imino aryl compound as well as preparation method, weeding composition and application thereof
  • Carboxylic acid derivative substituted imino aryl compound as well as preparation method, weeding composition and application thereof
  • Carboxylic acid derivative substituted imino aryl compound as well as preparation method, weeding composition and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0164] The following examples serve to illustrate the invention and should not be construed as limiting the invention in any way. The protection scope of the present invention is described by the claims.

[0165]In view of the economy and diversity of the compounds, we preferably synthesized some compounds. Among the synthesized compounds, selected parts are listed in Table 1 and Table A below. The specific compound structures and corresponding compound information are shown in Table 1 and Table A. The compounds in Table 1 and Table A are just to better illustrate the present invention, but do not limit the present invention. For those skilled in the art, it should not be understood that the scope of the above subject of the present invention is limited to the following compounds.

[0166] Table 1 Compound structure and its 1 HNMR

[0167]

[0168]

[0169]

[0170]

[0171]

[0172]

[0173]

[0174]

[0175]

[0176]

[0177]

[0178]

...

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 belongs to the technical field of pesticides, and particularly relates to a carboxylic acid derivative substituted imino aryl compound, a preparation method thereof, a weeding composition and application. The compound is shown as a ralgene formula I, wherein Q represents Y represents halogen, halogenated alkyl or cyano; Z represents halogen; M represents CH or N; W represents OX5, SX5 or N (X5) 2; X represents -CX < 1 > X < 2 >-(alkyl) n-,-alkyl-CX < 1 > X < 2 >-(alkyl) n-or-(CH2) r-; and X3 and X4 each independently represent O, S, NH, N-alkyl or the like. The compound has excellent herbicidal activity against grassy weeds, broadleaf weeds, cyperaceae weeds and the like even at a low application rate, and has high selectivity against crops.

Description

technical field [0001] The invention belongs to the technical field of pesticides, and specifically relates to an iminoaryl compound substituted by a carboxylic acid derivative, a preparation method thereof, a herbicidal composition and application thereof. Background technique [0002] The control of weeds is a crucial link in the process of realizing high-efficiency agriculture. Although there are various types of herbicides on the market, such as patent WO00 / 50409, etc. disclose the general formula compound 1-aryl-4-thiotriazine as a herbicide WO95 / 06641 discloses substituted 1-amino-3-phenyluracil compounds with herbicidal activity, and WO95 / 25725 discloses pyrimidyl aryl ketoxime compounds with herbicide and insecticide activity. However, the herbicidal properties of these known compounds against harmful plants and the selectivity against crops are not entirely satisfactory. And due to the continuous expansion of the market, the resistance of weeds, the service life of...

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): C07D251/38C07D405/12C07D409/12C07D403/12C07D413/12C07D417/12C07D401/12C07D403/04C07D405/04C07D401/06C07D405/06C07D239/54C07D239/56C07D239/545A01N43/66A01N47/06A01N43/76A01N43/78A01N43/80A01N43/836A01N47/36A01N43/54A01N47/12A01N43/56A01N43/653A01N43/647A01N43/58A01P13/00
CPCC07D251/38C07D405/12C07D409/12C07D403/12C07D413/12C07D417/12C07D401/12C07D403/04C07D405/04C07D401/06C07D405/06C07D239/54C07D239/56C07D239/545A01N43/66A01N47/06A01N43/76A01N43/78A01N43/80A01N43/82A01N47/36A01N43/54A01N47/12A01N43/56A01N43/653A01N43/647A01N43/58C07D409/10C07D239/22A01P13/02A01N33/18A01N33/22A01N35/10A01N37/22A01N37/26A01N37/40A01N41/10A01N43/08A01N43/40A01N43/50A01N43/60A01N43/68A01N43/70A01N43/707A01N43/84A01N43/88A01N43/90A01N47/22A01N47/30A01N47/38A01N57/14A01N57/20C07D401/04A01P13/00
Inventor 连磊华荣保彭学岗赵德崔琦
Owner QINGDAO KINGAGROOT CHEM COMPOUNDS 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