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1989
DOI: 10.3987/com-89-4901
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Synthesis of 3-Carboethixy-4-oxo-4H-pyrimido[1',2':1,5][1,2,4]triazolo[3,4-b]benzoxazole and 5H-Pyrido[3",2":5',6']pyrimido[1',2':1,5][1,2,4]triazolo[3,4-b]benzoxazole-5-one: Novel Heterocycles

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Cited by 13 publications
(16 citation statements)
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“…In this system a part of the heterocyclic moiety (1,2,4-triazole) is incorporated with the Schiff base comprising a heterodiene system and attribute as 4π component in Diels-Alder reactions. [4 + 2] cycloaddition reaction was carried out by dropwise addition of a solution of phenylacetyl chloride or diphenylacetyl chloride in dry 1,4-dioxan to a cold, stirred solution of 3benzylidineamino [1,2,4]triazole in dry 1,4-dioxan and triethylamine for a period of 30 min. After the complete addition of acid chloride, the reaction mixture was stirred for a further period of 8 h at 80°C (Fig.…”
Section: Resultsmentioning
confidence: 99%
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“…In this system a part of the heterocyclic moiety (1,2,4-triazole) is incorporated with the Schiff base comprising a heterodiene system and attribute as 4π component in Diels-Alder reactions. [4 + 2] cycloaddition reaction was carried out by dropwise addition of a solution of phenylacetyl chloride or diphenylacetyl chloride in dry 1,4-dioxan to a cold, stirred solution of 3benzylidineamino [1,2,4]triazole in dry 1,4-dioxan and triethylamine for a period of 30 min. After the complete addition of acid chloride, the reaction mixture was stirred for a further period of 8 h at 80°C (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Cultures of the test fungi were grown on PDA for 7 days at Figure 1. Synthesis of 5,7-Disubstituted [1,2,4] triazolo [1,5-a] pyrimidin-6-one derivatives by [4+2] cycloaddition reaction. Table 1 Physical data of 5,7-diaryl- [1,2,4]-triazolo [1,5-a]pyrimidin-6-one (3a-g)and 5,5,7-triaryl- [1,2,4]-triazolo [1,5-a]pyrimidin-6-one(4a-g).…”
Section: Resultsmentioning
confidence: 99%
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