1991
DOI: 10.3987/com-90-5622
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Pyridazine Derivatives and Related Compounds Part 5. Pyrazolo[3,4-c]pyridazine: Synthesis and Some Reactions

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Cited by 12 publications
(5 citation statements)
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“…and superimposable IR) with an authentic sample synthesised unambiguously by acetylation of the 3-amino-4,5-diphenyl-1H-pyrazolo [3,4-c]pyridazine with acetic anhydride. 9 Analogous results were obtained when the diazo compound 1 was irradiated in dimethyl sulfoxide, dimethyl formamide and in morpholine, where 8-10 were produced, respectively. The structures of photoproducts 8-10 were elucidated on the basis of spectral data and analytical results.…”
mentioning
confidence: 64%
See 1 more Smart Citation
“…and superimposable IR) with an authentic sample synthesised unambiguously by acetylation of the 3-amino-4,5-diphenyl-1H-pyrazolo [3,4-c]pyridazine with acetic anhydride. 9 Analogous results were obtained when the diazo compound 1 was irradiated in dimethyl sulfoxide, dimethyl formamide and in morpholine, where 8-10 were produced, respectively. The structures of photoproducts 8-10 were elucidated on the basis of spectral data and analytical results.…”
mentioning
confidence: 64%
“…162°C (dec), was prepared from the corresponding 3-amino derivative, as reported previously. 8 General procedure for photochemical reactions A sample of compound 1 in the appropriate anhydrous solvent/ reagent, was irradiated until the starting material disappeared. After removing the solvent under reduced pressure, the residue was recrystallised from an appropriate solvent.…”
Section: Methodsmentioning
confidence: 99%
“…244-245 °C) according to the reported procedures [7] by refluxing 3-chloro-5,6-diphenylpyridazine-4-carbonitrile 1 with hydrazine hydrate for 3 hours, (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of 3-amino-4,5-diphenyl-1H-pyrazolo [3,4-c]pyridazine 2 (Scheme 1) [7], and azobenzene compounds 3a-e and 4a-i [8], were conducted according to known procedures. Spectral data for compounds 3a-e and 4a-i were described in the previous parts (Scheme 2 and 3) [9,10].…”
Section: Synthesismentioning
confidence: 99%
“…Heterocyclic systems containing pyrazole and imidazole rings are characterized by several biological properties (Avasthi et al, 2002(Avasthi et al, , 2003 including a medicinal character which can be utilized in the management of inflammation (Deeb et al, , 1991Tisler and Stanounic, 1973;Seada et al, 1989). Various synthetic routes have been followed for synthesizing the fused ring pyrazolo-pyridazine system and their derivatives (Druey, 1958;Caronna et al, 1986;Kobayashi et al, 1971;Kasuga et al, 1974;Shawali, 1977;Kurihara et al, 1980).…”
Section: Introductionmentioning
confidence: 99%