A kind of triazine compound and its application in controlling chicken coccidiosis

A triazine compound and the technology of the compound are applied in the triazine compound and its application field in the control of chicken coccidiosis, which can solve the problems of increasing the difficulty and inconvenience of preparation preparation, high concentration of use, and easy drug resistance, etc., and achieve Good preventive and curative effect

Active Publication Date: 2011-12-21
SHANGHAI VETERINARY RES INST CHINESE ACAD OF AGRI SCI
View PDF3 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In terms of application, diclazuril is mainly used for the prevention of coccidiosis; it can also be used for treatment, but it is easy to produce drug resistance; In the treatment of coccidiosis, it is also prone to drug resistance
[0008] In terms of physical and chemical properties, diclazuril is almost insoluble in common solvents such as water and ethanol (edited by the Chinese Veterinary Pharmacopoeia Committee, the 2005 edition of the Veterinary Pharmacopoeia of the People's Republic of China, China Ag

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 triazine compound and its application in controlling chicken coccidiosis
  • A kind of triazine compound and its application in controlling chicken coccidiosis
  • A kind of triazine compound and its application in controlling chicken coccidiosis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] 2-{3-methyl-4-(4'-nitrophenoxy)phenyl}-1,2,4-triazine-3,5(2H,4H)-dione (compound of formula (I) ) preparation

[0034] Add compound Ⅱ (15 grams, 0.068mol), anhydrous sodium carbonate (7.9 grams, 0.075mol), p-chloronitrobenzene (11.8 grams, 0.075mol) and DMF (150ml) into a four-necked flask and heat to 120°C After reacting for 10 hours, after cooling down to room temperature, the reaction solution was poured into 1000ml of water, adjusted to pH=3 with 10% dilute hydrochloric acid, and a pale yellow solid was precipitated, filtered, washed with water, and dried to obtain the compound of formula (I) (16.2 g, 69.5%)

[0035] mp: 169 – 171.5°C. ESI-MS (m / z): 339.2(M-H) - , 1HNMR (CDCl 3): 2.25 (s, 3H), 7.00 (d, 2H), 7.09 (d, 1H), 7.44(d,1H), 7.50(s,1H), 7.60(s,1H), 8.22(d,2H) , 9.69 (s, 1H).

Embodiment 2

[0037] 2-{3-methyl-4-(4'-nitrophenoxy)phenyl}-1,2,4-triazine-3,5(2H,4H)-dione (compound of formula (I) ) preparation

[0038] Compound II (15 g, 0.068 mol), anhydrous potassium carbonate (10.4 g, 0.075 mol), p-chloronitrobenzene (11.8 g, 0.075 mol) and DMSO (100 ml), were added to a four-necked flask and heated to 130°C After reacting for 8 hours, after cooling down to room temperature, the reaction solution was poured into 1000ml of water, adjusted to pH=3 with 10% dilute sulfuric acid, and a pale yellow solid was precipitated, filtered, washed with water, and dried to obtain the compound of formula (I) (15 g, 64.3%).

Embodiment 3

[0040] Preparation of 2-(3-methyl-4-hydroxyphenyl)-1,2,4-triazine-3,5(2H,4H)-diketonol sodium salt

[0041] Compound Ⅱ (150 g, 0.68 mol), 500 g toluene, heated to dissolve, 30% sodium methoxide solution was added dropwise, a yellow powder was precipitated, filtered, washed with methanol, and dried to obtain 2-(3-methyl-4-hydroxybenzene base)-1,2,4-triazine-3,5(2H,4H)-diketone sodium salt (147.5 g, 90%).

[0042] ESI-MS (m / z): 218.1(M-Na) - .

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 compound represented by a formula (I) and application thereof to chicken coccidiosis disease control. The compound represented by the formula (I) is obtained by condensation of a compound represented by a formula (II) or sodium phenolate thereof with a compound represented by a formula (III) under the alkaline condition, wherein a substituent group x in the compound represented by the formula (III) is halogen. The compound represented by the formula (I) has the effects of preventing and treating a chicken coccidiosis disease, and has good chicken coccidiosis resisting activity when in concentration of 0.5-20mg/kg.

Description

technical field [0001] The present invention relates to compound and the application of compound, especially a kind of new triazine compound and its application in controlling chicken coccidiosis, and the synthesis method of the compound. Background technique [0002] Chicken coccidiosis is an intracellular parasitic disease mainly caused by intestinal lesions caused by one or several Eimeria chickens. It is a highly contagious parasitic disease that can cause chicken growth rate and The reduction of feed conversion rate and the decline of meat and egg quality. In severe cases, it can cause death of chickens. According to statistics, the incidence of coccidiosis in chickens is 50-70%, and the outbreak mortality rate reaches 20-30%. The economic loss caused by chicken coccidiosis in the world reaches 5 billion US dollars every year. my country is a big chicken raising country, accounting for 10% of the world's total chicken raising, and the direct and indirect economic loss...

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): C07D253/075A61K31/53A61P33/00A23K1/16
CPCA23K1/1612A23K1/1628A61K31/53A23K1/1826C07D253/075A23K20/111A23K20/137A23K50/75A61P33/00
Inventor 张丽芳薛飞群费陈忠韩春周张可煜郑文丽王霄旸王米孟新宇裘敏琪
Owner SHANGHAI VETERINARY RES INST CHINESE ACAD OF AGRI SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap