CAS: 65412-03-5; 4-(2-Aminoethyl)Tetrahydro-2H-Pyran

该化合物是一种多用途的地雷化合物,其特点是四氢丙烯(oxane)环,与乙胺协会相连,这种结构具有平衡的亲脂性和极性,使它成为制药和农用化学合成中有价值的中间体.它的氧气环增强了稳定性,而主要地雷群体则为进一步的功能化提供了反应性,如氨化形成或再消化.该化合物的僵硬但灵活的脚架对于药物发现特别有用,以调节物理化学特性和生物利用率.由于对地雷的敏感性,它通常在惰性条件下处理.对于研究和工业应用来说,它是一个可靠的建筑块,可以用来进行热循环和生物活性分子的发展.

结构式图片

相似化合物

389621-77-6 1314961-38-0 1083216-46-9

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号29943-42-8 四氢吡喃酮 | CAS号2537-48-6 氰甲基磷酸二乙酯 | CAS号40500-10-5 四氢-2H-吡喃-4-丙酸

合成工艺路线路线简述

    📜4-氰基甲基四氢吡喃置于palladium On Activated Charcoal,氢气体系中,用 乙醇 作为反应溶剂,25.0 °C,1.0 Mpa 条件下,反应 12.0H,以76.1%的收率获得产物4-(2-氨乙基)四氢吡喃
    参考文献:一种4-(2-氨乙基)四氢吡喃的合成方法
    标题:一种4-(2-氨乙基)四氢吡喃的合成方法
    摘要:本发明属于化学药物中间体的合成技术领域,具体涉及一种药物贝福普兰中间体4‑(2‑氨乙基)四氢吡喃的合成方法.该方法包括如下步骤:(1)4‑氯四氢吡喃与氰乙酸甲酯反应得到2‑氰基‑2‑(四氢‑4‑吡喃基)乙酸甲酯;(2)2‑氰基‑2‑(四氢‑4‑吡喃基)乙酸甲酯脱酯得到(四氢‑4‑吡喃基)‑乙腈;(3)(四氢‑4‑吡喃基)‑乙腈 C加氢反应得到4‑(2‑氨乙基)四氢吡喃.该方法采用4‑氯四氢吡喃,氰乙酸甲酯为原料,该方法反应时间短,成本较低,原料易得,无剧毒管制及不稳定的化学原料,安全有效,产率较高,杂质较少.

    海关参考信息

    专利信息


    专利号:US-2025129021-A1
    优先权日:2023-09-19
    标 题:Small molecule protein synthesis modulators
    发明人:GYGI DAVID; BAHMANYAR SOGOLE SAMI; HAMANN LAWRENCE
    权利人:INTERDICT BIO INC
    摘要:The present disclosure provides compounds of the formulae herein (e.g., Formula (I), Formula (V)), and pharmaceutically acceptable salts thereof, which are useful for modulating protein synthesis (e.g., modulating synthesis of BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D). The present disclosure also provides pharmaceutical compositions and kits comprising the compounds, or pharmaceutically acceptable salts thereof, and methods of treating or preventing diseases or disorders (e.g., diseases or disorders associated with BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D) by administering to a subject in need thereof the compounds, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.

    专利号:US-7468375-B2
    优先权日:2004-04-26
    标题:Inhibitors of the HIV integrase enzyme
    发明人:DRESS KLAUS RUPRECHT; HU QIYUE; JOHNSON TED WILLIAM; PLEWE MICHAEL BRUNO; TANIS STEVEN PAUL; WANG HAI; YANG ANLE; YIN CHUNFENG; ZHANG JUNHU
    权利人:PFIZER
    摘要:The present invention is directed to compounds of formula (I), and pharmaceutically acceptable salts and solvates thereof, their synthesis, and their use as modulators or inhibitors of the human immunodeficiency virus (“HIVâ€?) integrase enzyme.

    专利号:EP-3103803-B1
    优先权日:2008-10-27
    标 题 :Intermediates for the synthesis of mtor kinase inhibitors

    专利号:EP-3660020-A1
    优先权日:2008-10-27
    标题 :Process for the synthesis of mtor kinase inhibitors

    专利号:EP-3103803-A1
    优先权日:2008-10-27
    标 题 :Intermediates for the synthesis of mtor kinase inhibitors

    专利号:EP-3660020-B1
    优先权日:2008-10-27
    标题:Process for the synthesis of mtor kinase inhibitors

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1134/s1070363217070313
    摘要:Arutyunyan NS, Nazaryan RL, Akopyan LA, Akopyan NZ, Panosyan GA, Gevorgyan GA. Synthesis and some transformations of 2-(4-isopropyl-2-methyl-2-ethyltetrahydro-2H-pyran-4-yl)ethanamine. Russian Journal of General Chemistry. 2017 Jul;87(7):1634–7. doi: 10.1134/s1070363217070313.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知