S[sub.N]Ar Reactions on 2-Amino-4,6-dichloropyrimidine-5-carbaldehyde
We report the experimental results of unexpected aromatic nucleophilic substitution reaction products on 2-amino-4,6-dichloropyrimidine-5-carbaldehyde. The isolated compounds are products of amination, solvolysis, and condensation processes under mild and environmentally friendly conditions, due to...
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Veröffentlicht in: | MolBank 2022-08, Vol.2022 (3) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report the experimental results of unexpected aromatic nucleophilic substitution reaction products on 2-amino-4,6-dichloropyrimidine-5-carbaldehyde. The isolated compounds are products of amination, solvolysis, and condensation processes under mild and environmentally friendly conditions, due to the influence of structural factors of the starting pyrimidine and a high concentration of alkoxide ions. This method allows the building of pyrimidine-based compound precursors of N-heterocyclic systems. |
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ISSN: | 1422-8599 1422-8599 |
DOI: | 10.3390/M1426 |