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Heterocyclizations with Tosylmethyl Isocyanide Derivatives. A New Approach to Substituted Azolopyrimidines
24
Citations
9
References
2005
Year
Derivative (Chemistry)DerivativesSubstituted AzolopyrimidinesHeterocyclicTosylmethyl IsocyanideBenzyltriethylammonium ChlorideNew ApproachOrganic ChemistryEfficient SynthesisChemistryHeterocycle ChemistryTosylmethyl Isocyanide DerivativesPharmacologyChemical DerivativeSynthetic Chemistry
An efficient synthesis of substituted azolopyrimidines such as pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidines, pyrimido[1,6-a]indoles, benzo[4,5]imidazo-[1,2-c]pyrimidines, an imidazo[1,2-c]pyrimidine, and pyrazolo[1,5-c]pyrimidines is described. The method involves the reaction of N-protected bromomethylazoles and tosylmethyl isocyanide (TosMIC) derivatives in nonanhydrous media. The study of the reaction conditions shows that the method is only successful under phase-transfer conditions (CH2Cl2/30% aq NaOH) using benzyltriethylammonium chloride as a catalyst.
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