摘要 |
An improved process is described for preparing a N-(substituted arylmethyl)-4-substituted-4-(disubstituted methyl)piperidine of formula (I): wherein R<SUP>1 </SUP>and R<SUP>2 </SUP>are independently selected from the group consisting of halogen, CF<SUB>3</SUB>, OCF<SUB>3</SUB>, OCHF<SUB>2</SUB>, OCF<SUB>2</SUB>CHF<SUB>2 </SUB>and SF<SUB>5</SUB>; and Z and B are independently selected from the group consisting of CH and N; as well as processes for preparing intermediates useful in the overall process.
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