CAS: 271-95-4; 1,2-Benzisoxazole

该化合物是一种杂交循环化合物,其特征为引信苯和异氧环系,其分子式为C8H7NO,表明碳,氢,氮和氧的存在.该化合物一般是白色的黄色晶状固体,以其芳香性能而闻名,有助于其稳定性和再活性. 1,2-Benzisoxolole在乙醇和二氯乙烷等有机溶剂中表现出中等溶解性,但水溶性较低.该化合物对医药化学具有兴趣,因为其潜在的生物活动,包括抗微生物和抗炎特性.此外,该化合物是各种药物和农用化学合成的一个建筑块.该杂物的存在具有独特的电子特性,因此成为进一步进行化学修改的宝贵目标.安全数据表明,与许多有机化合物一样,它应谨慎处理,因为如果吸入或吸入,可能会对健康造成危害.

结构式图片

相似化合物

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合成工艺路线路线简述

    (E)-2-羟基苯甲醛肟置于三苯基膦,偶氮二甲酸二乙酯体系中,用 四氢呋喃 用作溶剂,化学反应 5.0H,以66%的收率获得1,2-苯异唑
    参考文献:6' Substituted Compounds Having 5-Ht6 Receptor Affinity
    标题:6' Substituted Compounds Having 5-Ht6 Receptor Affinity
    摘要:本公开提供了具有亲和力的化合物,其对5-Ht6受体具有亲和力,其化学式为(i): 其中r1-R4,A,B,D,E和g如本文所定义.该公开还涉及制备这种化合物的方法,含有这种化合物的组合物,以及这些化合物的使用方法.

    海关参考信息

    专利信息


    专利号:US-11548898-B2
    优先权日:2017-07-06
    标题 :Synthesis of halichondrins
    发明人:KISHI YOSHITO; AI YANRAN; YE NING; WANG QIAOYI; YAHATA KENZO; ISO Kentaro; NAINI SANTHOSH REDDY; YAMASHITA SHUJI; LEE JIHOON; OHASHI ISAO; FUKUYAMA TAKASHI
    权利人:HARVARD COLLEGE; EISAI R&D MAN CO LTD
    摘要:The present invention provides methods for the synthesis of ketones involving a Ni/Zr-mediated coupling reaction. The Ni/Zr-mediated ketolization reactions can be used in the synthesis of halichondrins (e.g., halichondrin A, B, C; homohalichondrin A, B, C; norhalichondrin A, B, C), and analogs thereof. Therefore, the present invention also provides synthetic methods useful for the synthesis of halichondrins, and analogs thereof. Also provided herein are compounds (i.e., intermediates) useful in the synthesis of halichondrins, and analogs thereof. In particular, the present invention provides methods and compounds useful in the synthesis of compound of Formula (H3-A).

    专利号:US-10889599-B2
    优先权日:2018-02-27
    标 题:1,1-diborylalkyl-1-metal compounds, preparation method thereof, and their applications toward synthesis of 1,1-diboronate ester compounds
    发明人:CHO SEUNG HWAN; LEE YEOSAN
    权利人:POSTECH ACAD IND FOUND
    摘要:The present invention relates to a 1,1-diborylalkyl-1-metal compound including one metal group together with two identical boron groups at the sp3 carbon center, and its use. Specifically, the present invention relates to development of novel organic reactions, synthesis of functional molecules, and synthesis of new drugs by applying the novel 1,1-diboryl-1-metal substituted alkyl compounds to various molecular libraries which could not be synthesized by conventional methodologies.

    专利号:US-8569560-B2
    优先权日:2006-10-13
    标题 :Synthesis of terminal alkenes from internal alkenes via olefin metathesis
    发明人:SCHRODI YANN; PEDERSON RICHARD L; KAIDO HIROKI; TUPY MICHAEL J
    权利人:ELEVANCE RENEWABLE SCIENCES
    摘要:This disclosure relates generally to olefin metathesis, and more particularly relates to the synthesis of terminal alkenes from internal alkenes using a cross-metathesis reaction catalyzed by an olefin metathesis catalyst. According to one aspect, for example, a method is provided for synthesizing a terminal olefin, the method comprising contacting, in the presence of a ruthenium alkylidene metathesis catalyst, an olefinic substrate comprised of at least one internal olefin with a cross metathesis partner comprised of an alpha olefinic reactant, under reaction conditions effective to allow cross-metathesis to occur, wherein the reaction conditions include a reaction temperature of at least 35° C. The methods, compositions, reactions and reaction systems herein disclosed have utility in the fields of catalysis, organic synthesis, and industrial chemistry.

    专利号:WO-0027627-A1
    优先权日:1998-11-12
    标题 :Aryloxime linkers in the solid-phase synthesis of 3-aminobenzisoxazoles
    发明人:WILEY MICHAEL ROBERT; LEPORE SALVATORE DONATO
    权利人:LILLY CO ELI; WILEY MICHAEL ROBERT; LEPORE SALVATORE DONATO
    摘要:In its first aspect, the invention is directed to a solid support mediated method for the synthesis of diverse polycyclic heterocycles according to general formula (V). A second aspect of the invention is directed to a solid support bound intermediate compound that optionally can be derivatized before a cyclization and displacement procedure provides a product. The intermediate is preferably stable to a wide range of chemical conditions thus allowing, if desired, for the chemical derivatization of the intermediate. A third aspect of the invention is directed to a library of polycyclic heterocycle compounds where said library contains a plurality of diverse library compounds of general formula (V). A fourth aspect of the invention is directed to a method for the synthesis of a library of diverse polycyclic heterocycles by the general method described. A fifth aspect of the invention is directed to an assay kit for the identification of lead compounds of the library described therein.

    专利号:WO-2024012791-A1
    优先权日:2022-07-11
    标题 :Electrochemical synthesis of pyrazolines and pyrazoles
    发明人:BÄR ROBIN MAXIMILIAN; FORD MARK JAMES; KALDAS SHERIF JAMES; WALDVOGEL SIEGFRIED; HOFMANN SILJA; LINDEN MARTIN
    权利人:BAYER AG
    摘要:The present invention relates to an electrochemical process for the synthesis of pyrazolines and pyrazoles of formula (I). The process can be especially used for the synthesis of the herbicide safener mefenpyr-diethyl.

    专利号:WO-2023102600-A1
    优先权日:2021-12-06
    标题:Synthesis of amphiphilic block copolymers and polymeric nanofibers produced therefrom
    发明人:ZETTERLUND PER B; ISHIZUKA FUMI; KIM HYUN JIN; CHATANI SHUNSUKE; NIINO HIROSHI
    权利人:NEWSOUTH INNOVATIONS PTY LTD
    摘要:The present disclosure relates to the field of synthesis of block copolymers, and polymeric nanofibers having a core-shell morphology produced therefrom. The present disclosure relates to the field of synthesis of block copolymers where one block is more hydrophobic than the other block and is a different composition. The disclosure also relates to uses of these polymeric nanofibers in various applications, such as reinforcing a polymeric matrix and for coatings applications.
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    主要参考文献


    1: Su MD. Theoretical investigations of the photochemical isomerizations of indoxazene and isoxazole. J Org Chem. 2009 Aug 21;74(16):6055-63. doi: 10.1021/jo901010q.

    合成参考文献


    参考文献:10.2165/11203810-000000000-00000
    摘要:Hoy SM, Scott LJ, Keating GM. Intramuscular paliperidone palmitate. CNS Drugs. 2010 Mar;24(3):227–44. doi: 10.2165/11203810-000000000-00000.
    参考文献:10.1016/j.bmc.2005.11.014
    摘要:Deng BL, Cullen MD, Zhou Z, Hartman TL, Buckheit RW, Pannecouque C, De Clercq E, Fanwick PE, Cushman M. Synthesis and anti-HIV activity of new alkenyldiarylmethane (ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs) incorporating benzoxazolone and benzisoxazole rings. Bioorg Med Chem. 2006 Apr 01;14(7):2366–74. doi: 10.1016/j.bmc.2005.11.014.
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