A mass spectrometric identification and differentiation of pyrimidin-4(3H)-and -4(lH)-ones was carried out. NSubstitution at position 1 or 3 made the distinction of tbe two sets of compounds very easy because of their characteristic fragmentation pathways. Most interesting were the spectra of the N-
Electron impact mass spectra of 1,3,4-thiadiazolo[3,2-a]pyrimidin-7-one and isomeric-5-one derivatives
✍ Scribed by S. Foti; F. Russo; A. Santagati; M. Santagati
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 401 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
The 70 eV electron impact mass spectra of some 1,3,4‐thiadiazolo[3,2‐a]pyrimidin‐7‐one and isomeric‐5‐one derivatives are discussed with the aid of defocused metastable spectra and exact mass measurements. The compounds are shown to be very stable to electron impact and ring contraction reactions are in most cases the characterstic fragmentations. Most importantly, the 7‐one derivatives fragment by a retro‐Diels–Alder process which does not occur in the 5‐one isomers. This provides a diagnostic tool for differentiation between the isomers and for the unequivocal assignment of the structure.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
The electron impact mass spectra of two series of 5-oxo-te~hydro-SH-tlriPzolo13,hl pyrimidine+ etbylcarboxylates and 7sxo-tetrahyBro-7H-thirzolo[ 3 , k l pyrimidine-6-ethykarboxylates were measured and fragmentation patterns examined. Structures were assigned from analysis of 0x0 molecular ion fragm