CAS: 10004-44-1; 5-Methylisoxazol-3(2H)-One

该化合物是一种环环有机化合物,在3级由羟基组取代,在5级由甲基组取代.这种结构具有独特的回活动性,使其成为制药和农用化学合成中有价值的中间体.它的功能组可以进行多种变异,包括核循环替代和凝聚,促进生物活性分子的开发.该化合物在标准条件下表现出稳定性,确保可靠的处理和储存.其定义明确的化学特性和与各种反应条件的兼容性使它成为设计新型治疗剂或作物保护化学品的研究人员的首选.该化合物的纯度和一贯性对于合成应用的再生效果至关重要.

结构式图片

相似化合物

2682-41-9 83014-80-6 930-83-6

欧盟法规

统一分类与标签ECHA物质ECHA物质工作场所安全标识要求食品接触材料-禁用CMR物质C&L通报欧盟农药活性物质化妆品禁用物质清单REACH预注册废弃物危险特性清单

上下游产品

CAS号141-97-9 乙酰乙酸乙酯 | CAS号87318-59-0 N-(trimethylsil... | CAS号10004-24-7 Ethyl tetrolate | CAS号674-82-8 双乙烯酮 | CAS号3075-23-8 3-Oxothiobutyri... | CAS号105-45-3 乙酰乙酸甲酯 | CAS号16864-45-2 3-甲氧基-5-甲基-异噁唑 | CAS号26347-19-3 2,5-dimethyl-4-... | CAS号127020-20-6 3-乙氧基-5-甲基异噁唑 | CAS号69513-43-5 2-(chloromethyl... | CAS号73028-21-4 2-benzyl-5-meth... | CAS号115886-00-5 3-benzyloxy-5-m... | CAS号54489-27-9 (3-Oxo-2,3-dihy...

合成工艺路线路线简述

    乙酰乙酸乙酯置于sodium Hydroxide,盐酸羟胺体系中,化学反应 1.0H,以61%的收率获得恶霉灵
    参考文献:Synthesis Of 3-Isoxazolols Revisited. Diketene And (β-Ketoesters As Starting Materials
    标题:Synthesis Of 3-Isoxazolols Revisited. Diketene And (β-Ketoesters As Starting Materials
    摘要:3-异噁唑醇可以通过β-酮酸酯或二酮乙烯和羟胺在非常好收率下制备,前提是在整个反应过程中保持ph值约为10,并且用过量的强矿酸淬灭反应混合物.这样可以抑制5-异噁唑酮的形成,否则这些通常是反应的主要产物.
    Doi:10.1139/v84-333

    专利信息


    专利号:US-6225329-B1
    优先权日:1998-03-12
    标 题 :Modulators of protein tyrosine phosphatases (PTPases)
    发明人:RICHTER LUTZ STEFAN; ANDERSEN HENRIK SUNE; VAGNER JOSEF; JEPPESEN CLAUS BEKKER; MOELLER NIELS PETER HUNDAHL; BRANNER SVEN; SU JING; BAKIR FARID; JUDGE LUKE MILBURN
    权利人:NOVO NORDISK AS
    摘要:The present invention provides novel compounds of Formula 1, compositions containing these compounds, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like, n wherein A, R 1 , R 2 , R 3 , R 4 , R 16 and R 17 are as defined in the specification. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:US-2005119332-A1
    优先权日:1998-03-12
    标 题 :Substituted thiophene compounds as modulators of protein tyrosine phosphatases (PTPases)
    发明人:JEPPESEN LONE; ANDERSEN HENRIK S; OLSEN OLE H; JUDGE LUKE M; HOLSWORTH DANIEL D; BAKIR FARID; AXE FRANK U; GE YU
    摘要:The present invention provides novel compounds of formula 1a, n nnovel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:WO-9946244-A1
    优先权日:1998-03-12
    标题 :Modulators of protein tyrosine phosphatases (ptpases)
    发明人:JEPPESEN LONE; ANDERSEN HENRIK SUNE; OLSEN OLE HVILSTED; JUDGE LUKE MILBURN; HOLSWORTH DANIEL DALE; BAKIR FARID; AXE FRANK URBAN; GE YU
    权利人:NOVO NORDISK AS; ONTOGEN CORP
    摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:US-6951878-B2
    优先权日:1998-03-12
    标 题:Benzo[b]thiophenyl or tetrahydro-benzo[b]thiophenyl modulators of protein tyrosine phosphatases (PTPases)
    发明人:MOELLER NIELS PETER HUNDAHL; ANDERSEN HENRIK SUNE; IVERSEN LARS FOGH; OLSEN OLE HVILSTED; BRANNER SVEN; HOLSWORTH DANIEL DALE; BAKIR FARID; JUDGE LUKE MILBURN; AXE FRANK URBAN; JONES TODD KEVIN; RIPKA WILLIAM CHARLES; GE YU; UYEDA ROY TERUYUKI
    权利人:NOVO NORDISK AS
    摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. n The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:WO-9946268-A1
    优先权日:1998-03-12
    标题 :MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPases)
    发明人:ANDERSEN HENRIK SUNE; JONES TODD KEVIN; HOLSWORTH DANIEL DALE
    权利人:NOVO NORDISK AS; ONTOGEN CORP
    摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPases) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:US-2002019412-A1
    优先权日:1998-03-12
    标题:Modulators of protein tyrosine phosphatases (ptpases)
    发明人:ANDERSEN HENRIK SUNE; JONES TODD KEVIN; HOLSWORTH DANIEL DALE
    摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
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    1: Zhang Y, Wei D, Wu X, Duan T, Xu J, Dong F, Pan X, Zheng Y. Occurrence and impact of carbendazim and hymexazol residues on yeast growth and ochratoxin A contamination during wine production. J Sci Food Agric. 2023 Oct;103(13):6280-6287. doi: 10.1002/jsfa.12699. Epub 2023 Jun 11. 57(40):15138-15152. doi: 10.1021/acs.est.2c03095. Epub 2023 Oct 2. 70(30):9520-9535. doi: 10.1021/acs.jafc.2c02507. Epub 2022 Jul 25. 7(9):685. doi: 10.3390/jof7090685.
    5: Antypenko L, Meyer F, Sadyk Z, Shabelnyk K, Kovalenko S, Steffens KG, Garbe LA. Combined Application of Tacrolimus with Cyproconazole, Hymexazol and Novel {2-(3-R-1H-1,2,4-triazol-5-yl)phenyl}amines as Antifungals: In Vitro Growth Inhibition and In Silico Molecular Docking Analysis to Fungal Chitin Deacetylase. J Fungi (Basel). 2023 Jan 5;9(1):79. doi: 10.3390/jof9010079.
    6: Deng H, Ma X, Wang Y, Zhou S, Li X, Li W, Liu Z. Preparation of multi- modified/carbonized/gelatinized starch and its de-risking effect on Cd(II) and hymexazol in wastewater. Int J Biol Macromol. 2024 Oct;278(Pt 2):134768. doi: 10.1016/j.ijbiomac.2024.134768. Epub 2024 Aug 14.

    合成参考文献


    摘要:Gigiena i Sanitariya. For English translation, see HYSAAV., 56(4)(53), 1991
    摘要:Guide to the Chemicals Used in Crop Protection., 6(302), 1973
    摘要:Japan Pesticide Information., (40)(32), 1982
    摘要:Gigiena i Sanitariya. For English translation, see HYSAAV., 55(5)(72), 1990
    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
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