CAS: 85006-25-3; Tert-Butyl (Tert-Butoxycarbonyl)Oxycarbamate

该化合物是一种化学化合物,其特性是其功能组,特别是氢氧辛基磺酸和两个三氧碳基(Boc)保护组,该化合物通常用于有机合成,特别是在化学反应期间保护氨和氢氧基胺.该化合物的存在增强了氢氧基胺的稳定性,使该物质在某些条件下的响应性较低,这在多步骤合成过程中是有利的.在酸性条件下可以去除三氧基碳基化合物,允许在需要时恢复活性氢氧基胺功能.该化合物一般是白色的对非白色固体,在有机溶剂中可溶解.其应用范围扩大到制药化学,可以作为各种生物活性分子合成的中间体.在处理该化合物时,应当注意安全防范措施,因为如果摄入或吸入,可能会对健康造成危害,而且应当使用适当的个人防护设备.

结构式图片

相似化合物

58377-44-9 36016-38-3 42989-85-5

欧盟法规

ECHA物质C&L通报REACH预注册

合成工艺路线路线简述

  • 合成目标产物 Tert-Butyl N-(Tert-Butoxycarbonyloxy)Carbamate 主要起始原料 Di-Tert-Butyl Dicarbonate And Hydroxylamine Hydrochloride
  • 24424-99-5 = 85006-25-3
    反应条件:1.1 Reagents: Triethylamine,Hydroxyamine Hydrochloride Solvents: Tert-Butyl Methyl Ether,Water
    标题:A Facile Synthesis Of N,O-Bis(Tert-Butoxycarbonyl)Hydroxylamine
    作者:Staszak,Michael A.; Et Al
    参考文献:Tetrahedron Letters 日期:1993 卷标:34(44) 页码:7043-4
二碳酸二叔丁酯置于盐酸羟胺,三乙胺体系中,用 水,Petroleum Ether 作为反应溶剂,以85%的收率获得产物n,O-二叔丁氧羰基-羟胺
参考文献:的简便合成ñ,ø-双(叔丁氧羰基)-羟胺
标题:的简便合成ñ,ø-双(叔丁氧羰基)-羟胺
摘要:N,O-二(叔丁氧羰基)羟胺在从盐酸羟胺和二-85%产率合成叔丁基二碳酸酯在三乙胺的存在下进行.该化学方法很容易,利用了现成的试剂,与以前公开的方法相比,安全性得到了提高.
DOI:10.1016/s0040-4039(00)61592-7

海关参考信息

专利信息


专利号:US-8987504-B2
优先权日:2010-06-18
标题 :Aminohydroxylation of alkenes
发明人:MEE SIMON PETER HAROLD; LUXENBURGER ANDREAS; HARRIS LAWRENCE DANIEL
权利人:MEE SIMON PETER HAROLD; LUXENBURGER ANDREAS; HARRIS LAWRENCE DANIEL; VICTORIA LINK LTD
摘要:The invention relates to a process for the aminohydroxylation of alkenes using N-oxycarbamate reagents, e.g. N-acyloxycarbamate, N-alkyloxycarbonyloxycarbamate and N-aralkoxycarbonyloxycarbamate reagents. The invention particularly relates to an intermolecular aminohydroxylation reaction that can be carried out in the absence of added base. The invention also relates to novel N-oxycarbamate reagents that are stable crystalline materials. The process of the invention is useful in the synthesis of compounds having a vicinal amino alcohol moiety, such as biologically active compounds.

专利号:US-2007099915-A1
优先权日:2005-10-07
标题 :Inhibitors of the hiv integrase enzyme
发明人:DRESS KLAUS R; JOHNSON TED W; PLEWE MICHAEL B; TANIS STEVEN P; ZHU HUICHUN
权利人:PFIZER
摘要:The present invention is directed to compounds of formula (I), n nand 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: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:US-2009170846-A1
优先权日:2005-10-03
标题 :Inhibitors of the hiv integrase enzyme
发明人:DRESS KLAUS RUPRECHT; PLEWE MICHAEL BRUNO; JOHNSON TED WILLIAM; TANIS STEVEN PAUL; TRAN KHANH TUAN
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. Formula (I).
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合成参考文献


摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 210.
摘要:Geffken, D.; Köllner, M. A., Science of Synthesis, (2009) 40, 939.
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