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Hydro-de-halogenation and consecutive deprotection of chlorinated N-amido-pyrrolidin-2-ones with Raney-Ni: an effective approach to gabapentin |
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| Authors: | Rita CagnoliFranco Ghelfi Ugo M PagnoniAndrew F Parsons Luisa Schenetti |
| Affiliation: | a Dipartimento di Chimica, Università degli Studi di Modena e Reggio Emilia, Via Campi 183, I-41100 Modena, Italy b Department of Chemistry, University of York, Heslington, York YO10 5DD, UK |
| Abstract: | The benzoylamino group was identified as a useful radical cyclization auxiliary that can be smoothly removed on hydro-de-halogenation of chlorinated N-substituted-pyrrolidin-2-ones with Raney-Ni. This methodology was successfully implemented in a new and appealing route to the anti-epileptic drug gabapentin. |
| Keywords: | hydrazides cyclizations pyrrolidinones hydrogenolysis |
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