Publication | Closed Access
Formylation and Bromination of Pyrrolo[2,1-<i>a</i>]isoquinoline Derivatives with Bromoisobutyrate and Dimethyl Sulfoxide
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Citations
44
References
2021
Year
Efficient FormylationDerivative (Chemistry)Dimethyl SulfoxideBioorganic ChemistryDerivativesCarbonyl ReagentNatural SciencesBromination ReagentOrganic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyPharmaceutical ChemistrySynthetic ChemistryNatural Product Synthesis
We have developed an efficient formylation of pyrroloisoquinolines using bromoisobutyrate and dimethyl sulfoxide as carbonyl reagent. Various formylated pyrroloisoquinolines could be prepared in good yields (up to 94%). This formylation process can be easily scaled up to gram scale with good yield. In most cases of pyrroloisoquinolines without methoxy groups, the combination of bromoisobutyrate and dimethyl sulfoxide could act as a bromination reagent, delivering brominated pyrroloisoquinolines in acceptable to good yields (up to 82%).
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