The title compound, C(18)H(33)N(3)O(5), was prepared from N-tert-butoxy-carbonyl-4-piperidone using a nine-step reaction, including condensation, methyl-ation, oximation, hydrolysis, esterification, ammonolysis, Hoffmann degradation, tert-butoxy-carbonyl protection and methyl-ation. The E configuration of the methyl-oxime geometry of the compound is confirmed.
tert-Butyl 3-[N-(tert-butoxy-carbonyl)methyl-amino]-4-methoxy-imino-3-methyl-piperidine-1-carboxyl-ate.
叔丁基 3-[N-(叔丁氧羰基)甲基氨基]-4-甲氧基亚氨基-3-甲基哌啶-1-羧酸酯
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作者:Wan Zhilong, Chai Yun, Liu Mingliang, Guo Huiyuan
| 期刊: | Acta Crystallographica Section E-Structure Reports Online | 影响因子: | 0.600 |
| 时间: | 2009 | 起止号: | 2009 Jan 8; 65(Pt 2):o256 |
| doi: | 10.1107/S1600536808044255 | ||
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