NMR Properties of 5,7-Disubstituted Derivatives of 1,2,4-Triazolo[1,5a] pyrimidines
✍ Scribed by A. Grodzicki; E. Szłyk; L. Pazderski; A. Goliński; J. G. Haasnoot
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 247 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Some 5,7-disubstituted derivatives of 1,2, 4-triatolo[l ,%]pyrimidines with methyl, tert-butyl, phenyl and trifluoromethyl substituents were studied. The syntheses and 'H, l3C* 1 6 N and lgF N M R and mass spectra are reported. Natural abundance 1 6 N N M R spectra and signal assignments, based on chemical shifts and selective decoupling experiments, are discussed. The influence of substituents on the chemical shifts of 'H, 13C, "N and "F signals was considered. '6N-'sF and "N-'H spin-spin couplings in relation to the structural changes caused by the substituents examined were characterized.
📜 SIMILAR VOLUMES
With sodium borohydride in tetrahydrofuran/ethanol (5 : 1). the product ( I ) gives a 75 yield of a compound, m.p. 233 "C, that is identical with the recently prepared 2-(diphenylmethyl)imidaz0le[~1. When product ( I ) is boiled for 2 h in tetrahydrofuran/water (2: I ) it affords 2-(hydroxy-dipheny