Regioselective synthesis of novel N2- and N4-substituted 7-methylpyrazolo[4,5-e][1,2,4]thiadiazines.

Autor: Liu X; Institute of Medicinal Chemistry, School of Pharmacy, Shandong University, Jinan 250012, PR China. xinyongl@sdu.edu.cn, Yan R, Chen N, Xu W, Molina MT, Vega S
Jazyk: angličtina
Zdroj: Molecules (Basel, Switzerland) [Molecules] 2006 Nov 01; Vol. 11 (11), pp. 827-36. Date of Electronic Publication: 2006 Nov 01.
DOI: 10.3390/11110827
Abstrakt: The new compound 7-methylpyrazolo[4,5-e][1,2,4]thiadiazin-3(2H,4H)-one1,1-dioxide (5) was synthesized and its novel mono N2- or N4-substituted derivatives 6 and 7 were prepared by regioselective N-alkylation of 5 with different molar ratios of NaH and alkyl halides. Based on the regioselective alkylation conditions found a facile one-pot synthesis of N2,N4-disubstituted pyrazolo[4,5-e][1,2,4] thiadiazines 8 was developed. The structures of the newly synthesized compounds were confirmed by IR,(1)H-NMR, (13)C-NMR and MS spectral analysis.
Databáze: MEDLINE