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Title:

A convenient route to 4-carboxy-4-anilidopiperidine esters and acids.

Document type:
Journal Article
Author(s):
Marton, J; Glaenzel, B; Roessler, J; Golaszewski, D; Henriksen, G
Abstract:
The route selection and development of a convenient synthesis of 4-carboxy-4-anilidopiperidines is described. Previous routes were hampered by the low yield of the target esters as well as the inability to convert the esters to the required free acids. Considerations for large-scale production led to a modified synthesis that utilised a tert-butyl ester of 4-carboxy-4-anilidopiperidines which resulted in a dramatic increase in the overall yield of the target N-propionylated- 4-anilidopiperidine-...     »
Journal title abbreviation:
Molecules
Year:
2012
Journal volume:
17
Journal issue:
3
Pages contribution:
2823-32
Language:
eng
Fulltext / DOI:
doi:10.3390/molecules17032823
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/22399137
Print-ISSN:
1420-3049
TUM Institution:
Klinik und Poliklinik für Nuklearmedizin
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