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

Application of 2-arylmorpholine and salt thereof serving as insecticide

An aryl morpholine salt and aryl morpholine technology are applied in the application field of 2-aryl morpholine and its salt as the preparation of pesticides, and can solve the problems of no research and development reports on the application and the like

Inactive Publication Date: 2011-09-14
HUNAN UNIV
View PDF7 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are no research and development reports on the application of 2-arylmorpholines and their salts as pesticides;

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
  • Application of 2-arylmorpholine and salt thereof serving as insecticide
  • Application of 2-arylmorpholine and salt thereof serving as insecticide
  • Application of 2-arylmorpholine and salt thereof serving as insecticide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 12

[0018] Preparation of embodiment 12-aryl morpholines and salts thereof

[0019] According to literature [Organic Chemistry, 2004, 24(8): 902-905; Applied Chemistry, 2005, 22(3): 343-345; Journal of Hunan University, 2004, 31(4): 11-14; 2005, 32( 4): 72-76] method to prepare 2-arylmorpholine and its salt (I).

[0020]

[0021] Among them, R 2 Selected from: H, OH or OR 1 , where R 1 Selected from: C 1 ~C 2 Alkyl, C 3 ~C 4 Straight chain alkyl or branched chain alkyl; R 3 From: H, C 1 ~C 2 Alkyl, C 3 ~C 4 Straight chain alkyl or branched chain alkyl; R 4 From: H, C 1 ~C 2 Alkyl, C 3 ~C 4 Straight chain alkyl or branched chain alkyl, hydroxyethyl, Ar'CH 2 , wherein Ar' is selected from: phenyl, 4-methoxyphenyl, 4-fluorophenyl, 4-chlorophenyl, 4-bromophenyl, 4-nitrophenyl, 4-aminophenyl, 4 -Acetamidophenyl, 2-methanesulfonylaminophenyl, 3-methanesulfonylaminophenyl, 4-methanesulfonylaminophenyl, 4-trifluoromethylphenyl, 4-isobutylphenyl or 6-methoxy-2-napht...

Embodiment 22

[0022] Example 22-Arylmorpholine or its salts are tested for poisonous activity against armyworm, broad bean aphid and cotton spider mite

[0023] 1 test target

[0024] Armyworm (My, thimna sepatara) is a sensitive strain that has been raised on fresh corn leaves for many years; the test insects are 3rd instar larvae; broad bean aphid (Aphis fabae) is a sensitive strain that has been raised on broad bean seedlings indoors for many years, and the test insects are 3-day The cotton spider mite (Tetranychus urticae) is a sensitive strain that has been raised indoors with broad bean seedlings for many years. The test insects were healthy adult mites.

[0025] 2 culture conditions

[0026] The culture conditions of the tested target and the target after the test are temperature 25±5° C., relative humidity 65±5%, and photoperiod 12 / 12h (L / D).

[0027]3 Test drug (original drug): 2-arylmorpholine or its salt.

[0028] 4 Preparation of the original drug: use an electronic balance ...

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 application of 2-arylmorpholine as shown in the chemical structural formula I or salt thereof serving as an insecticide. The formula I is shown in the specification, wherein, R<2> is chosen from H, OH or OR<1>, and R<1> is chosen from C1-C2 alkyl and C3-C4 linear alkyl or branched alkyl; R<3> is chosen from H, C1-C2 alkyl and C3-C4 linear alkyl or branched alkyl; R<4> is chosen from H, C1-C2 alkyl, C3-C4 linear alkyl or branched alkyl, ethoxyl and benzyl; R<5> is chosen from H, C1-C2 alkyl, C3-C4 linear alkyl or branched alkyl, phenyl or substituted phenyl; Ar is chosen from phenyl, substituted phenyl or 6-methoxy-2-naphthyl; and the salt of the 2-arylmorpholine is chosen from hydrochloride, hydrobromate, sulphate, nitrate or phosphate.

Description

technical field [0001] The present invention relates to the application of a class of compounds as the preparation of insecticides, in particular to the application of 2-arylmorpholine and its salts as the preparation of insecticides. Background technique [0002] Shao Ling et al. described that 4-aryl-5-triazolylthiazole-2-imine compounds have fungicidal activity against Pleurotus spp. (Chemical Journal of Chinese Universities, 2007, 28, 270). He Daohang et al. described the synthesis and bactericidal activity of 4-aryl-2-(2-hydroxybenzimino)thiazole [Journal of South China University of Technology, Natural Science Edition, 2008, (3): 60]; Chinese patent (CN 101602761) describes The bactericidal activity of 4-tert-butyl-5-(1,2,4-triazol-1-yl)-2-benziminothiazole; Chinese patents (CN 101653127, CN 101632366) described a Alcohol or pyrimethol and morpholine fungicide pesticide composition, the pesticide composition has fungicidal activity on the prevention and treatment of a...

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): A01N43/84A01P7/04A01P7/02A01P13/00
Inventor 胡艾希周溪石磊叶姣窦杰
Owner HUNAN UNIV
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