6533b874fe1ef96bd12d5ff3
RESEARCH PRODUCT
Mass spectrometry of 3,4-dihydroquinazolin-4-ones of pharmaceutical interest. Part3. Electron ionization mass spectra of 2-substituted-3-(5′-pyrazolyl)-4(3H)-quinazolinones
Mirella FerrugiaSalvatore PlesciaM. L. BajardiLeopoldo Ceraulosubject
chemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Organic ChemistryPolyatomic ionMass spectrumPhysical chemistryPyrazoleMass spectrometryElectron ionizationSpectral lineIondescription
The fragmentation reactions induced by electron impact of eighteen title compounds has been investigated with the aid of low beam energy spectra (14 eV, nom. value), metastable ion detection, high resolution measurements and labelling experiments. The loss of the 4-carbonyl oxygen together with the 3-substituent, which constitutes a characteristic fragmentation route of 3-aryl and 3-heteroaromatic substituted-4(3H)-quinazolinones, is again observed, but the presence of a carboxyethyl group at the 4′-position of the pyrazole ring is responsible of an anomalous loss of 47 daltons from the molecular ion. Lastly, a comparison with the previously described behaviour of 3-(5′-isoxazolyl) derivatives was carried out.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1992-03-01 | Journal of Heterocyclic Chemistry |