Starting from amino(di)azines and 2-chloro-6-methyliso(thio)cyanate a series of aryl-substituted urea and thiourea derivatives was prepared and screened as potential antiepileptics. Among the new derivatives tested, only 2b and 3c exhibited adequate anticonvulsant effects, whereas 3d and 4d were fou
The synthesis and larvicidal activity of N -aroyl- N ′-(5-aryl-2-furoyl)ureas
✍ Scribed by Yang, Xin-Ling; Wang, Dao-Quan; Chen, Fu-Heng; Zhang, Zhong-Ning
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 147 KB
- Volume
- 52
- Category
- Article
- ISSN
- 1526-498X
No coin nor oath required. For personal study only.
✦ Synopsis
A novel type of diarolyurea compound containing a furan ring has been designed and prepared. Thus, a series of N-aroyl-N@-(5-aryl-2-furoyl)ureas were synthesized by a nucleophilic addition reaction between 5-substituted furamide and aroyl isocyanate in high yield ([80%). Their structures were con-Ðrmed by IR, [1H]NMR and elemental analyses. Bioassay showed that some of them exhibited activity against second-instar larvae of the yellow fever mosquito (Aedes aegypti L.). With the aid of artiÐcial neural network combined with multivariable regression, a preliminary study was made of structureÈactivity relationship.
1998 SCI.
📜 SIMILAR VOLUMES
## Abstract We describe the synthesis of __N__‐aryl‐2‐methyl‐3‐carbethoxy‐5‐pyrrolinones benzylidene derivatives, their condensation with azomethines and substitution with aniline. The compounds have been tested for antimicrobial and fungicide activity: they have better fungicidal than bactericidal
## Abstract Isatin and 5‐methylisatin were condensed with various aryloxyacetylhydrazides to furnish the 3‐(aryloxyacetylhydrazono)‐5‐alkylindolin‐2‐ones **1–4**. When **1–4** were subjected to __Mannich__ reaction, the __N,N__‐disubstituted 1‐(aminomethyl)‐5‐alkyl‐3‐(aryloxyacetylhydrazono)indolin
## Abstract The synthesis of N‐[5‐(2‐phenoxyphenyl)‐1, 3, 4‐oxadiazole‐2‐yl]‐N′‐phenylurea derivatives is reported. The structures of these compounds are supported by their IR, ^1^H‐NMR and mass spectra. Conformational analysis and superimposition of energy minima conformers of these compounds on L
In view of the isosterism of the sulfonyl group(-SO 2 -) and the phosphoryl group, two new types of compounds N-(N-aryl-O-alkyl phosphoryl)-NЈ-(4,6dimethoxypyrimidin-2-yl) ureas (2) and N-(N-aryl-Nalkylphosphoryl) -NЈ -(4, 6 -dimethoxypyrimidin -2-yl) ureas (3) were designed and synthesized by treat