SYNTHESIS OF 4,7-DIHYDRO[1,2,4]TRIAZOLO[1,5-<i>a</i>]PYRIMIDINE-6-SULFONAMIDE DERIVATIVES
DOI:
https://doi.org/10.1007/2511Keywords:
4, 7-dihydro[1, 2, 4]triazolo[1, 5-a]pyrimidine-6-sulfonamides, 1-(1-piperidinylsulfonyl)acetones, alkylation, metalation, three-component condensationAbstract
A three-component condensation of 1-(1-piperidinylsulfonyl)acetones, aromatic aldehydes, and 3-amino-1,2,4-triazole in DMF leads to the formation of 5-alkyl-6-(1-piperidinylsulfonyl)-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine derivatives. If 4-nitrobenzaldehyde is employed, 5-methyl-7-(4-nitrophenyl)[1,2,4]triazolo[1,5-a]pyrimidine is the single isolated reaction product. The starting 1-(1-piperidinylsulfonyl)acetones were obtained from 1-(methylsulfonyl)piperidine in sequential metalation with n-butyllithium, reaction with aliphatic aldehydes, and oxidation of the obtained sulfoalcohols.
How to Cite
Kolosov, M. A.; Al-Ogaili, M. J. K.; Kulyk, O. G.; Orlov, V. D. Chem. Heterocycl. Compd. 2015, 51, 691. [Khim. Geterotsikl. Soedin. 2015, 51, 691.]
For this article in the English edition see DOI 10.1007/s10593-015-1759-5