CAS: 152120-54-2; Tert-Butyl (((Tert-Butoxycarbonyl)Amino)(1H-Pyrazol-1-yl)Methylene)Carbamate

该化合物是一种化学化合物,其独特结构包括一个丙烯环和两个丁氧碳酸基(Boc)保护组,该化合物通常用于有机合成和医药化学,特别是用于药品的开发.Boc组在反应过程中保护矿物质功能,允许有选择地修改双甲醇.N,N'Bis-Boc-1-guanylpyrarole因其潜在的生物活动而闻名,经常作为合成瓜尼丁衍生物的前体,可以展示各种药用特性.该化合物在标准实验室条件下一般稳定,但可能需要特定的处理和储存以保持其完整性.其溶解性因所使用的溶剂而异,在理想的合成途径中考虑其再活性十分重要.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号24424-99-5 二碳酸二叔丁酯 | CAS号152120-61-1 N-B°C-1H-吡唑-1-甲脒 | CAS号4023-02-3 1H-吡唑-1-甲脒盐酸盐 | CAS号4023-00-1 吡唑-1-羧酰胺 | CAS号143824-77-5 N-芴甲氧羰基-N',N''-... | CAS号1143571-96-3 Carbamic acid, ... | CAS号41651-87-0 4-[(hydrazinylm...

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-7067554-B2
    优先权日:2000-05-30
    标 题 :Method for the synthesis of compounds of formula I and their uses thereof
    发明人:MJALLI ADNAN M M; GOPALASWAMY RAMESH; AVOR KWASI A; WYSONG CHRISTOPHER L; ANDREW PATRON
    权利人:TRANSTECH PHARMA INC
    摘要:This invention provides certain compounds, methods of their preparation, pharmaceutical compositions comprising the compounds, their use in treating human or animal disorders. The compounds of the invention are useful as modulators of the interaction between the receptor for advanced glycated end products (RAGE) and its ligands, such as advanced glycated end products (AGEs), S100/calgranulin/EN-RAGE, β-amyloid and amphoterin, and for the management, treatment, control, or as an adjunct treatment for diseases in humans caused by RAGE. Such diseases or disease states include acute and chronic inflammation, the development of diabetic late complications such as increased vascular permeability, nephropathy, atherosclerosis, and retinopathy, the development of Alzheimer's disease, erectile dysfunction, and tumor invasion and metastasis.

    专利号:US-9550000-B2
    优先权日:2011-09-09
    标题 :Compositions, methods, and systems for the synthesis and use of imaging agents
    发明人:ROBINSON SIMON P; YU MING
    权利人:ROBINSON SIMON P; YU MING; LANTHEUS MEDICAL IMAGING INC
    摘要:The present invention relates to systems, compositions, and methods for the synthesis and use of imaging agents, or precursors thereof. An imaging agent precursor may be converted to an imaging agent using the methods described herein. In some cases, the imaging agent is enriched in 18 F. In some cases, an imaging agent may be used to image an area of interest in a subject, including, but not limited to, the heart, cardiovascular system, cardiac vessels, brain, and other organs. In some embodiments, methods and compositions for assessing perfusion and innervation mismatch in a portion of a subject are provided.

    专利号:US-2004053999-A1
    优先权日:1997-09-17
    标题 :Novel compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; DAHL TERRENCE C; HITCHCOCK MICHAEL J M; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; MILLS ROGER G; WILLIAMS MATTHEW A
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:US-6225341-B1
    优先权日:1995-02-27
    标 题:Compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; WILLIAMS MATTHEW A
    权利人:GILEAD SCIENCES INC
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:WO-2022260918-A1
    优先权日:2021-06-07
    标 题:Composition and method for dual targeting in treatment of neuroendocrine tumors
    发明人:MOUSA SHAKER; RAJABI MEHDI; KARAKUS OZLEM O
    权利人:NANOPHARMACEUTICALS LLC
    摘要:Chemical compositions and methods of synthesis thereof. The compositions disclosed and described herein are directed toward thyroid hormone ανβ3 integrin receptor antagonists conjugated to targets of the norepinephrine transporter (NET) or the catecholamine transporter. The compositions have a dual targeting effect and increased targeting efficiency in the treatment and diagnostic imaging of neuroendocrine tumors.

    专利号:US-2023065387-A1
    优先权日:2019-10-14
    标题:Synthesis of tyrosine kinase inhibitors
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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Design And Synthesis Of Short Amphiphilic Cationic Peptidomimetics Based On Biphenyl Backbone As Antibacterial Agents
    作者:Rajesh Kuppusamy,Muhammad Yasir,Thomas Berry,Charles G. Cranfield,Shashidhar Nizalapur,Eugene Yee,Onder Kimyon,Aditi Taunk,Kitty K.K. Ho,Bruce Cornell,Mike Manefield,Mark Willcox,David Stc Black,Naresh Kumar |发布日期:2018.1
    摘要:Antimicrobial Peptides (Amps) And Their Synthetic Mimics Have Received Recent Interest As New Alternatives To Traditional Antibiotics In Attempts To Overcome The Rise Of Antibiotic Resistance In Many Microbes. Amps Are Part Of The Natural Defenses Of Most Living Organisms And They Also Have A Unique Mechanism Of Action Against Bacteria. Herein, A New Series Of Short Amphiphilic Cationic Peptidomimetics

    合成参考文献


    摘要:Simmons, N.; Chheda, P.; Schuman, D., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 404.
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