25-06-2014 дата публикации
Номер: CN103880746A
Принадлежит:
The invention relates to a chemical synthetic method for (s)-3-(Boc-amino)azacycloheptane. The (s)-3-(Boc-amino)azacycloheptane is synthesized through esterification, cyclization, reduction, protection and deprotection by taking L-lysine as a raw material. The method comprises the steps of adding L-lysine into ethanol, adding a catalyst concentrated sulfuric acid, reacting to a reflux state, and esterifying to prepare L-lysine ester; adding the L-lysine ester into ethanol, and reacting to synthesize (s)-3-aminocyclocaprolactam; adding (s)-3-aminocyclocaprolactam and lithium aluminum hydride into a tetrahydrofuran solvent, reacting and controlling to be in a reflux state, and performing reduction reaction to obtain (s)-3-amino-azacycloheptane; reacting to prepare (s)-3-(N'-cbz-amino)-1-N-cbz-azacycloheptane; reacting to obtain (s)-3-(N'-Boc-N'-cbz-amino)-1-N-cbz-azacycloheptane; reacting to obtain the (s)-3-(Boc-amino)azacycloheptane. The synthesis method utilizes the chirality of amino ...
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