CAS: 887587-15-7; 3-Ethylamino-Pyrrolidine-1-Carboxylic Acid Tert-Butyl Ester

该化合物是有机合成的多用途中间体,对制造含氮乙酸循环极有价值,其保护的氨基磺酸组确保在各种反应条件下保持稳定,同时允许在必要时有选择地取消保护.乙基氨基替代体增强了其在医药化学中的用途,使药物发现应用能够进一步发挥作用.该复合体表现出高纯度和一贯性能,适合用于浸泡物的改造,催化剂开发和制药研究.其明确界定的结构和活性特征有助于高效合成途径,减少侧面反应,提高多步工艺的产量.

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CAS号75-07-0 乙醛 | CAS号147081-49-0 (R)-(+)-N-叔丁氧羰基...

合成工艺路线路线简述

    📜3-氨基吡咯烷-1-羧酸叔丁酯置于palladium 10% On Activated Carbon,氢气,Sodium Hydride,N,N-二异丙基乙胺体系中,用 乙醇,二氯甲烷,N,N-二甲基甲酰胺 作为反应溶剂,20.0 °C,101.33 Kpa 条件下,反应 3.0H,反应生成 3-(乙基氨基)-1-吡咯烷甲酸叔丁酯
    参考文献:Discovery Of Quinazoline-2,4(1H,3H)-Dione Derivatives As Novel Parp-1/2 Inhibitors: Design,Synthesis And Their Antitumor Activity
    标题:Discovery Of Quinazoline-2,4(1H,3H)-Dione Derivatives As Novel Parp-1/2 Inhibitors: Design,Synthesis And Their Antitumor Activity
    摘要:新型喹唑啉-2,4(1H,3H)-二酮衍生物,带有3-氨基吡咯烷基团,被确认为具有独特结合特性的有效parp-1/2抑制剂.
    DOI:10.1039/c8Ob00286J

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    专利信息


    专利号:US-8030501-B2
    优先权日:2006-07-28
    标题 :Process for producing optically active 3-amino nitrogen-containing compounds
    发明人:OHNUKI MASATOSHI; IZUMIDA MASASHI; NISHIYAMA AKIRA; MATSUMOTO SHINGO
    权利人:KANEKA CORP
    摘要:Aiming at production of an optically active 3-amino nitrogen-containing compound which is useful as an intermediate in synthesis of medicines and pesticides, in particular, an optically active 1-protected-3-aminopyrrolidine derivative, from an inexpensive and readily available raw material by a process which is efficient and can be practiced industrially, an optically active 3-amino nitrogen-containing compound is produced by performing a reaction of an optically active 3-substituted nitrogen-containing compound with ammonia, methylamine, ethylamine or dimethylamine in the presence of water. In addition, a 1-protected-3-aminopyrrolidine derivative is produced by performing a reaction of an optically active 1-protected-3-(sulfonyloxy)pyrrolidine derivative with ammonia, methylamine, ethylamine, or dimethylamine in the presence of methanol, ethanol, n-propanol, or isopropanol under a pressure of less than 30 barr.

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    合成参考文献

    参考DOI号:10.1039/c8ob00286j
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