Your browser doesn't support javascript.
loading
Pyridine Derivatives as Insecticides. Part 5. New Thieno[2,3-b]pyridines and Pyrazolo[3,4-b]pyridines Containing Mainly Ethyl Nicotinate Scaffold and Their Insecticidal Activity toward Aphis gossypii (Glover,1887).
Abuelhassan, Suzan; Abdel-Rahman, Abdu E; Gad, Mohamed A; Youssef, Mohamed A M; Abdel-Hafez, Shams H; Bakhite, Etify A.
Afiliación
  • Abuelhassan S; Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.
  • Abdel-Rahman AE; Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.
  • Gad MA; Research Institute of Plant Protection, Agriculture Research Center, Giza 12112, Egypt.
  • Youssef MAM; Research Institute of Plant Protection, Agriculture Research Center, Giza 12112, Egypt.
  • Abdel-Hafez SH; Department of Chemistry, College of Science, Taif University, Taif 21944, Saudi Arabia.
  • Bakhite EA; Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.
J Agric Food Chem ; 72(31): 17271-17282, 2024 Aug 07.
Article en En | MEDLINE | ID: mdl-39052523
ABSTRACT
Ethyl 5-cyano-1,6-dihydro-2-methyl-4-(2'-thienyl)-6-thioxonicotinate (A) was synthesized and reacted with ethyl chloroacetate in the presence of sodium acetate or sodium carbonate to give ethyl 5-cyano-6-((2-ethoxy-2-oxoethyl)thio)-2-methyl-4-(2'-thienyl)nicotinate (1a) or its isomeric thieno[2,3-b]pyridine 2a. 3-Aminothieno[2,3-b]pyridine-2-carboxamide 2b was also synthesized by the reaction of A with 2-chloroacetamide. The reaction of 1a with hydrazine hydrate in boiling ethanol gave acethydrazide 3. Heating ester 1a with hydrazine hydrate under neat conditions afforded 3-amino-1H-pyrazolo[3,4-b]pyridine 10. Compounds 2b, 3, and 10 were used as precursors for synthesizing other new thieno[2,3-b]pyridines and pyrazolo[3,4-b]pyridines containing mainly the ethyl nicotinate scaffold. Structures of all new compounds were confirmed by elemental and spectral analyses. Most of the obtained compounds were evaluated for their insecticidal activity toward the nymphs and adults of Aphis gossypii (Glover,1887). Some compounds such as 4, 9b, and 9c showed promising results. The effect of some sublethal concentrations, less than LC50, of compounds 4, 9b, and 9c on the examined Aphis was subjected to a further study. The results demonstrated that exposure of A. gossypii nymphs to sublethal concentrations of compounds 4, 9b, and 9c had noticeable effects on their biological parameters, i.e., nymphal instar duration, generation time, and adult longevity. The highest concentration C1 of all three compounds increased the nymphal instar duration and generation time and decreased adult longevity and vice versa.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Áfidos / Piridinas / Insecticidas Límite: Animals Idioma: En Revista: J Agric Food Chem Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Áfidos / Piridinas / Insecticidas Límite: Animals Idioma: En Revista: J Agric Food Chem Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos