n-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazole-2-yl]amide and its preparation and application

A technology of thiazole and phenyl, which is applied in the field of preparation and application of N-[4-phenyl-5-thiazol-2-yl]amide, can solve the problems of high price and strong irritation, and achieve good anticancer active effect

Inactive Publication Date: 2018-03-23
HUNAN UNIV
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] In this bromination reaction, NBS has high selectivity, but it has a strong irritant and is relatively expensive

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
  • n-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazole-2-yl]amide and its preparation and application
  • n-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazole-2-yl]amide and its preparation and application
  • n-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazole-2-yl]amide and its preparation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Preparation of 2-bromo-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)ethanone

[0038] Add 0.1mol of 1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)ethanone, 3mL of acetic acid, and 0.14mol of sodium bromide into the reaction flask, and stir at 70°C , add 0.3mol30% hydrogen peroxide dropwise, and react for 3.0h; Rate 85.0%. 1 H NMR (CDCl 3 , 400MHz) δ: 8.80 (s, 1H, triazole 5-H), 8.03 (s, 1H, triazole 3-H), 7.71 (s, 1H, CH), 7.66 (d, J=8.0Hz, 1H , C 6 h 3 6-H), 7.52(d, J=8.0Hz, 1H, C 6 h 3 3-H), 7.44~7.42(m, 1H, C 6 h 3 5-H).

Embodiment 2

[0040] Preparation of 2-bromo-1-(2,4-dichloro-5-fluorophenyl-2-(1,2,4-triazol-1-yl)ethanone

[0041] 0.1mol 1-(2,4-dichloro-5-fluorophenyl)-2-(1,2,4-triazol-1-yl)ethanone, 3mL acetic acid, 0.14mol sodium bromide were added to the reaction flask, 70 Stir at ℃, add 0.3mol30% hydrogen peroxide dropwise, react for 3.0h; get 2-bromo-1-(2,4-dichloro-5-fluorophenyl)-2-(1,2,4-triazole-1 -base) ethyl ketone, yield 88.0%. 1 H NMR (CDCl 3 , 400MHz) δ: 8.76 (s, 1H, triazole 5-H), 8.03 (s, 1H, triazole 3-H), 7.73 (s, 1H, CH), 7.59~7.54 (m, 2H, C6H23, 6-H).

Embodiment 3

[0043] Preparation of 4-(2,4-dichloro-5-fluorophenyl)-5-(1,2,4-triazol-1-yl)thiazol-2-amine

[0044] 1mmol 2-bromo-1-(2,4-dichloro-5-fluorophenyl)-2-(1,2,4-triazol-1-yl)ethanone, 20mL ethanol, reflux, add 1mmo l Thiourea, monitored by TLC, reacted for 10 minutes, cooled to 40°C, added dropwise dilute ammonia water to pH=7-8, and filtered with suction to obtain light yellow solid 4-(2,4-dichloro-5-fluorophenyl)-5- (1,2,4-Triazol-1-yl)thiazol-2-amine, yield 80.3%, m.p.251-253°C. 1 H NMR (CDCl 3 , 400MHz) δ: 8.02 (s, 1H, triazole 5-H), 7.94 (s, 1H, triazole 3-H), 7.49~7.47 (m, 1H, phenyl 3-H), 7.26~7.25 ( m, 1H, phenyl 6-H), 5.78 (s, 2H, NH 2 ).

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
wavelengthaaaaaaaaaa
Login to view more

Abstract

The present invention relates to N-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazole-2-yl]amide shown in chemical structural formula I: wherein, X1, X3 are selected from: chlorine , bromine, fluorine, iodine; X4 is selected from: hydrogen, deuterium, methyl, ethyl, chlorine, bromine, fluorine, iodine; X2, X5 is selected from: hydrogen, deuterium, methyl, ethyl; R is selected from: hydrogen , methyl; n is selected from: 0, 1, 2, 3; Y is selected from: hydrogen, C1 ~ C2 alkyl, C3 ~ C11 straight chain alkyl or branched chain alkyl, C1 ~ C2 haloalkyl or dihaloalkyl , C3-C5 halogenated straight chain alkyl or halogenated branched chain alkyl, phenyl. N-[4-phenyl-5-(1,2,4-triazole-1-yl)thiazol-2-yl]amide is used in the preparation of anticancer drugs or neuraminidase inhibitors for Hela cells.

Description

technical field [0001] The present invention relates to the preparation and application of novel compounds, specifically the preparation and application of N-[4-phenyl-5-(1,2,4-triazol-1-yl)thiazol-2-yl]amide. Background technique [0002] 2-Bromo-1-phenyl-2-(1,2,4-triazol-1-yl)ethanone is the preparation of 4-phenyl-5-(1,2,4-triazol-1-yl) - The key intermediate of 1,3-thiazol-2-amine and its derivatives. The preparation of 2-bromo-1-phenyl-2-(1,2,4-triazol-1-yl)ethanone and its use in the synthesis of thiazole derivatives has been described [J.Organomet.Chem. 2006, 691: 2686; Synth.Commun.2007, 37: 199; Heteroat Chem 2007, 18: 55; Chemical Journal of Higher Schools, 2007, 28: 270-273; Organic Chemistry, 2012, 32: 1715-1718]. Fang Jianxin et al. describe bromination of 1-phenyl-2-(1,2,4-triazol-1-yl)ethanone with molecular bromine in acetic acid to obtain 2-bromo-1-phenyl-2-(1 , 2,4-triazol-1-yl) ethanone; The preparation reaction is as follows: [0003] [0004] In t...

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): C07D417/04A61K31/427A61P35/00A61P31/16
Inventor 胡艾希张明明丁娜叶姣颜晓维向建南
Owner HUNAN UNIV
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