Preparation method of cycleanine

The invention provides a preparation method of cycleanine, and belongs to the field of organic synthesis. The invention provides a preparation method of cycleanine, which comprises the following reaction steps: a 1, 4, 7, 10-tetraazacyclododecane derivative is contacted with a carbonyl reducing agen...

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Hauptverfasser: ZHANG TANGZHI, KYOITSU, LU QIAN
Format: Patent
Sprache:chi ; eng
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Zusammenfassung:The invention provides a preparation method of cycleanine, and belongs to the field of organic synthesis. The invention provides a preparation method of cycleanine, which comprises the following reaction steps: a 1, 4, 7, 10-tetraazacyclododecane derivative is contacted with a carbonyl reducing agent to obtain cycleanine, the 1, 4, 7, 10-tetraazacyclododecane derivative is a compound with at least one carbon atom on the ring of 1, 4, 7, 10-tetraazacyclododecane being oxo, and the carbonyl reducing agent is a compound with at least one carbon atom on the ring of 1, 4, 7, 10-tetraazacyclododecane being oxo. The carbonyl reducing agent is lithium aluminum hydride, sodium borohydride or potassium borohydride. According to the technical scheme, the invention provides a brand-new cycleanine synthesis route which does not involve a ring-closing reaction and has high yield. 本发明提供了一种轮环藤宁的制备方法,属于有机合成领域。本发明提供了一种轮环藤宁的制备方法,包括如下反应步骤:将1,4,7,10-四氮杂环十二烷衍生物与羰基还原剂接触,得到轮环藤宁,其中,1,4,7,10-四氮杂环十二烷衍生物为1,4,7,10-四氮杂环十二烷的环上至少一个碳原子被氧代的化合