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A General and Efficient Synthesis of Sulfonylbenzotriazoles from <i>N</i>-Chlorobenzotriazole and Sulfinic Acid Salts
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Citations
17
References
2004
Year
Chemical EngineeringEnantioselective SynthesisEngineeringHeterocyclicOrganometallic ReagentsOrganic ChemistryEfficient SynthesisChemistryHeterocycle ChemistryStereoselective SynthesisCorresponding SulfonamidesSynthetic ChemistrySulfinic Acid Salts
One-pot reactions of sulfinic acid salts (produced from organometallic reagents with SO2) with N-chlorobenzotriazole gave the corresponding N-alkane-, N-arene-, and N-heteroenesulfonylbenzotriazoles 3a-j in 41-93% yields. Reagents 3a-j are efficient sulfonylating agents, reacting at 20-80 degrees C with various primary and secondary aliphatic amines to yield the corresponding sulfonamides in 64-100% yields.
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