tert-Butyl 4-carbamoyl-3-methoxy­imino-4-methyl­piperidine-1-carboxyl­ate

The title compound, C(13)H(23)N(3)O(4), was prepared starting from ethyl N-benzyl-3-oxopiperidine-4-carboxyl­ate through a nine-step reaction, including hydrogenation, Boc (tert-butoxy­carbon­yl) protection, methyl­ation, oximation, hydrolysis, esterification and ammonolysis. In the crystal structur...

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Detalles Bibliográficos
Autores principales: Wang, Juxian, Liu, Mingliang, Cao, Jue, Wang, Yucheng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960090/
https://www.ncbi.nlm.nih.gov/pubmed/21581272
http://dx.doi.org/10.1107/S1600536808036106
Descripción
Sumario:The title compound, C(13)H(23)N(3)O(4), was prepared starting from ethyl N-benzyl-3-oxopiperidine-4-carboxyl­ate through a nine-step reaction, including hydrogenation, Boc (tert-butoxy­carbon­yl) protection, methyl­ation, oximation, hydrolysis, esterification and ammonolysis. In the crystal structure, mol­ecules are linked by inter­molecular N—H⋯O hydrogen bonds to form a porous three-dimensional network with solvent-free hydro­phobic channels extending along the c axis.

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