The multistep synthesis of two pyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-one derivatives, a new class of fused 1,2,3,5-tetrazepinones with potential antiproliferative activity, has been carried out. Owing to the instability of the above compounds, the last step of the synthesis was performed at -5/0 degrees C. The obtained tetrazepinones, when allowed to stand at r.t. for 24 h, afforded quantitatively 1-phenyl-3,6-dimethylpyrazolo [3,4-d][1,2,3] triazole.

MAGGIO B, RAFFA D, RAIMONDI MV, PLESCIA F, CASCIOFERRO S, DAIDONE G (2006). Synthesis of alkyl-5,8-dimethyl-6-phenyl-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-ones of pharmaceutical interest. ARKIVOC, XV, 120-126 [http://dx.doi.org/10.3998/ark.5550190.0007.f14].

Synthesis of alkyl-5,8-dimethyl-6-phenyl-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-ones of pharmaceutical interest

MAGGIO, Benedetta;RAFFA, Demetrio;RAIMONDI, Maria Valeria;PLESCIA, Fabiana;CASCIOFERRO, Stella Maria;DAIDONE, Giuseppe
2006-01-01

Abstract

The multistep synthesis of two pyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-one derivatives, a new class of fused 1,2,3,5-tetrazepinones with potential antiproliferative activity, has been carried out. Owing to the instability of the above compounds, the last step of the synthesis was performed at -5/0 degrees C. The obtained tetrazepinones, when allowed to stand at r.t. for 24 h, afforded quantitatively 1-phenyl-3,6-dimethylpyrazolo [3,4-d][1,2,3] triazole.
2006
MAGGIO B, RAFFA D, RAIMONDI MV, PLESCIA F, CASCIOFERRO S, DAIDONE G (2006). Synthesis of alkyl-5,8-dimethyl-6-phenyl-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-ones of pharmaceutical interest. ARKIVOC, XV, 120-126 [http://dx.doi.org/10.3998/ark.5550190.0007.f14].
File in questo prodotto:
File Dimensione Formato  
Synthesis of alkyl-5,8-dimethyl-6-phenyl-5,6-dihydropyrazolo[3,4-f].pdf

Solo gestori archvio

Dimensione 222.14 kB
Formato Adobe PDF
222.14 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
06-2179GP.pdf

accesso aperto

Dimensione 226.01 kB
Formato Adobe PDF
226.01 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/19902
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 5
social impact