UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES
HUSSEIN, A., ABDEL HAFIZ, I., KHODAIR, A., BAKER, S., HUSSEIN, A. (2008). UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES. EKB Journal Management System, 2008(12), 119-134. doi: 10.21608/absb.2008.10502
A. HUSSEIN; I. S. ABDEL HAFIZ; A. E. KHODAIR; SAFAA M. BAKER; A. M. HUSSEIN. "UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES". EKB Journal Management System, 2008, 12, 2008, 119-134. doi: 10.21608/absb.2008.10502
HUSSEIN, A., ABDEL HAFIZ, I., KHODAIR, A., BAKER, S., HUSSEIN, A. (2008). 'UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES', EKB Journal Management System, 2008(12), pp. 119-134. doi: 10.21608/absb.2008.10502
HUSSEIN, A., ABDEL HAFIZ, I., KHODAIR, A., BAKER, S., HUSSEIN, A. UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES. EKB Journal Management System, 2008; 2008(12): 119-134. doi: 10.21608/absb.2008.10502

UTILITY OF N-2-PYRIDYL–3-OXOBUTANAMIDE IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF NEW DIHYDROPYRIDINE, FUSED PYRIDINE, PYRIDOPYRIDONE, PYRIDAZINE AND PYRIDOPYRIMIDINETHIONE DERIVATIVES

Al-Azhar Bulletin of Science
Article 1, Volume 2008, Issue 12, December 2008, Pages 119-134    PDF (343.69 K)
Document Type: Original Article
DOI: 10.21608/absb.2008.10502
Authors
A. HUSSEIN1; I. S. ABDEL HAFIZ* 2; A. E. KHODAIR3; SAFAA M. BAKER2; A. M. HUSSEIN1
1Department of Chemistry, Faculty of Science, Al Azhar University, Assiut 71524, Egypt.
2Department of Chemistry, Faculty of Education, Suez Canal University, Al-ArisH, Egypt.
3Department of Chemistry, Faculty of Science, Suez Canal University, ismailia, Egypt.
Abstract
2-Aminopyridine was fused with ethyl acetoacetate for two hours to yield the N-2-pyridyl–3-oxobutanamide (1). However, when the reaction time was increased to 5 hours compound 3 was obtained. Condensation of 3 with benzaldehyde gave 4. The reaction of pyridopyridone 3 with arylidenemalononitrile 7a-c afforded 4H-pyran derivatives 10a-c. In contrast to the behavior of arylidenemalononitriles 7a-c towards pyridopyridine 3, benzylidenemalononitrile 7d reacted with compound 3 to give the product 11. Compound 1 was allowed to react with arylidenemalononitriles  to give the dihydropyridine derivatives 17a-d. Alkylation of compound 1 with alkylating agents has been also reported. Thus, compound 1 was condensed with [DMF-DMA] in refluxing dioxane to yield 18, but under the reaction conditions we obtained only 21. The pyridopyridone 3 reacted with benzoyl isothiocyanates 25a,b to give thiourea derivatives 26a,b. Cyclization of 26a,b in dry dioxane and conc. sulphuric acid afforded pyridopyrimidine-2-thione derivatives 27a,b. On the other hand, coupling of pyridopyridone 3 with the aryl diazonium salts 28a-e afforded the corresponding azo products 29a-e. Boiling of compound 29 in ethanol and HCl afforded the azo products 30a-e. Treatment of arylhydrazone 30a with malononitrile afforded the pyridazine derivative 31.
Keywords
Pyridine; pyridopyridone; pyridazine; pyridopyrimidinethione derivatives
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