CAS: 931-03-3; 1H-Pyrrole-3-Carboxylic Acid

该化合物是一种有机化合物,其特点是其火花环结构,即五人组成的含有一个氮原子的芳香热循环,该化合物在火花环的三处有一个碳盒酸功能组(COOH),该组有助于其酸性. 糖浆-3-碳盒酸通常是一种白色到浅黄色的固体,由于存在碳盒酸组,在水和酒精等极溶剂中溶解. 它显示出了五人种含有一个氮原子的芳香气循环的典型特性,包括火瓶衍生物和碳盒酸的特性,包括各种化学反应和恐吓等化学反应中的潜在再活动.这一化合物对各个领域都感兴趣,包括医药化学和材料科学领域,因为它可能从事生物活动,并且用于合成更为复杂的有机分子.此外,它可能作为合成药物和农用化学物的建筑块.与许多有机化合物一样,处理应该谨慎,并遵循适当的安全议定书.

结构式图片

相似化合物

7126-39-8 2703-17-5 7126-38-7

欧盟法规

ECHA物质C&L通报

上下游产品

3-吡咯甲酸甲酯 Methyl 1H-Pyrrole-3-Carboxylate 2703-17-5
乙基 1H-吡咯-3-羧酸 Ethyl 1H-Pyrrole-3-Carboxylate 37964-17-3
吡咯-3-甲醛 Pyrrole-3-Carboxaldehyde 7126-39-8

合成工艺路线路线简述

  • 合成目标产物 Pyrrole-3-Carboxylic Acid 主要起始原料 Methyl 1H-Pyrrole-3-Carboxylate
  • 1013405-49-6 = 931-03-3
    反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Acetonitrile,Water; 24 H,Rt
    标题:A New Synthetic Route To 3-Polyfluoroalkyl-Containing Pyrroles
    作者:Shaitanova,Elena N.; Gerus,Igor I.; Kukhar,Valery P.
    参考文献:Tetrahedron Letters 日期:2008 卷标:49(7) 页码:1184-1187]

    931-03-3 = 931-03-3
    反应条件:1.1 Reagents: Cupric Chloride; 3 H,Rt
    标题:Coordinated Molecularly Imprinted-Based Ratiometric Sensor For Electrochemical Sensing Of Hazardous Ciprofloxacin Based On Nitrogen And Sulfur Co-Doped Porous Carbon/silver Nanoparticles Hybrid
    作者:Mahmoud,Ashraf M.; Abu-Alrub,Samer S.; Al-Qarni,Ali O.; Alshareef,F. M.; El-Wekil,Mohamed M.
    参考文献:Microchemical Journal 日期:2023 卷标:193]

    93362-49-3 = 931-03-3 [标题:Reaction Conditions
    标题:Product Subclass 14: Aryllithium And Hetaryllithium Compounds
    作者:Gribble,Gordon W.
    参考文献:Science Of Synthesis 日期:2006 卷标:8 页码:357-426]

    87630-35-1 = 931-03-3 [标题:Reaction Conditions
    标题:N-(Triisopropylsilyl)Pyrrole. A Progenitor "Par Excellence" Of 3-Substituted Pyrroles
    作者:Bray,Brian L.; Mathies,Peter H.; Naef,Reto; Solas,Dennis R.; Tidwell,Thomas T.; Et Al
    参考文献:Journal Of Organic Chemistry 日期:1990 卷标:55(26) 页码:6317-28]

    = 931-03-3 [标题:Reaction Conditions
    标题:Screening Of A Custom-Designed Acid Fragment Library Identifies 1-Phenylpyrroles And 1-Phenylpyrrolidines As Inhibitors Of Notum Carboxylesterase Activity
    作者:Mahy,William; Patel,Mikesh; Steadman,David; Woodward,Hannah L.; Atkinson,Benjamin N.; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2020 卷标:63(17) 页码:9464-9483]

    = 931-03-3 [标题:Reaction Conditions
    标题:Functionalization Of 2-Trifluoromethyl-1H-Pyrrole: A Convenient Entry Into Advanced Fluorinated Building Blocks Including All Isomeric 2-(Trifluoromethyl)Prolines
    作者:Hys,Vasyl Yu.; Shevchuk,Oleksandr I.; Vashchenko,Bohdan V.; Karpenko,Oleksandr V.; Gorlova,Alina O.; Et Al
    参考文献:European Journal Of Organic Chemistry 日期:2020 卷标:2020(25) 页码:3896-3905]

    = 931-03-3 [标题:Reaction Conditions
    标题:Structure Of Batrachotoxin,A Steroidal Alkaloid From The Colombian Arrow Poison Frog,Phyllobates Aurotaenia,And Partial Synthesis Of Batrachotoxin And Its Analogs And Homologs
    作者:Tokuyama,Takashi; Daly,J.
    参考文献:Journal Of The American Chemical Society 日期:1969 卷标:91(14) 页码:3931-8]

    106058-86-0 = 931-03-3
    反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Water
    标题:A Facile And Efficient Synthesis Of Pyrrole-3-Carboxylic Acid From Pyrrole
    作者:Cativiela,Carlos; Garcia,Jose I.
    参考文献:Organic Preparations And Procedures International 日期:1986 卷标:18(4) 页码:283-5]

    134439-96-6 = 931-03-3
    反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Methanol,Water; Rt -> Reflux; 4 H,Reflux1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 1
    标题:Synthesis Of Pyrrole-3-Carboxylic Acid
    作者:Liu,Zhi-Da; Teng,Da-Wei
    参考文献:Yingyong Huagong 日期:2013 卷标:42(5) 页码:860-862]

    7126-39-8 = 931-03-3
    反应条件:1.1 Reagents: Sodium Hypochlorite Catalysts: Sodium Hydroxide Solvents: Water; 1 H,100 °C; 100 °C -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 3 - 4,Rt
    标题:Oxidation Of Aldehydes And Alcohols To Carboxylic Acids Using Naclo Under Microwave Irradiation Or Classical Heating Without A Catalyst
    作者:Pujol,Maria Dolors; Navarro,Lorena
    参考文献:Letters In Organic Chemistry 日期:2018 卷标:15(6) 页码:534-539]

    = 931-03-3
    反应条件:1.1 Reagents: Lithium Tert-Butoxide Solvents: Dimethylformamide; 24 H,100 °C; Cooled1.2 Reagents: Hydrochloric Acid Solvents: Water; Cooled
    标题:Synthesis Of Cyclic Chiral α-Amino Boronates By Copper-Catalyzed Asymmetric Dearomative Borylation Of Indoles
    作者:Chen,Lili; Shen,Jun-Jian; Gao,Qian; Xu,Senmiao
    参考文献:Chemical Science 日期:2018 卷标:9(26) 页码:5855-5859]

    85684-93-1 = 931-03-3 [标题:Reaction Conditions
    标题:Product Class 13: 1H-Pyrroles
    作者:Black,D. Stc.
    参考文献:Science Of Synthesis 日期:2002 卷标:9 页码:441-552]

    7126-39-8 = 931-03-3
    反应条件:1.1 Reagents: Silver Oxide (Ag2O)
    标题:Studies Of The Maillard Reaction. I. Reaction Of Amino Sugars With Malondialdehyde
    作者:Gomez-Sanchez,Antonio; Maya,Ines; Hermosin,Isidro
    参考文献:Carbohydrate Research 日期:1990 卷标:200 页码:167-80]

    85684-93-1 = 931-03-3
    反应条件:1.1 Reagents: Ammonia Solvents: Methanol
    标题:The Protecting-Directing Role Of The Trityl Group In Syntheses Of Pyrrole Derivatives: Efficient Preparations Of 1H-Pyrrole-3-Carboxylic Acid And 3-Acyl-,3-Amino-,And 3-Bromo-1-Tritylpyrroles
    作者:Chadwick,Derek J.; Hodgson,Simon T.
    参考文献:Journal Of The Chemical Society 日期:1983 卷标:(1) 页码:93-102]

    = 931-03-3 [标题:Reaction Conditions
    标题:Preparation Of Novobiocin Analogs Having Modified Glycoside Moieties As Antitumor Agents
    参考文献:United States]

    = 931-03-3 [标题:Reaction Conditions
    标题:3-Lithiopyrroles By Halogen-Metal Interchange Of 3-Bromo-1-(Triisopropylsilyl)Pyrroles. Synthesis Of Verrucarin E And Other 3-Substituted Pyrroles
    作者:Muchowski,Joseph M.; Naef,Reto
    参考文献:Helvetica Chimica Acta 日期:1984 卷标:67(4) 页码:1168-72]

    = 931-03-3 + 634-97-9
    反应条件:1.1 Reagents: Chlorodimethylaluminum Solvents: Toluene,Hexane; 3 H,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Rt1.3 Reagents: Sodium Carbonate Solvents: Water; Rt1.4 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Rt
    标题:Carboxylation Of Indoles And Pyrroles With Co2 In The Presence Of Dialkylaluminum Halides
    作者:Nemoto,Koji; Onozawa,Satoru; Egusa,Naoki; Morohashi,Naoya; Hattori,Tetsutaro
    参考文献:Tetrahedron Letters 日期:2009 卷标:50(31) 页码:4512-4514
📜3-氰基吡咯置于sodium Hydroxide,Sodium Amide体系中,用 甲苯 作为反应溶剂,化学反应 10.0H,反应生成 3-吡咯羧酸
参考文献:Pyrrole-3-Carbamidine:来自 Nierembergia Hippomanica 的致死原理
标题:Pyrrole-3-Carbamidine:来自 Nierembergia Hippomanica 的致死原理
摘要:摘要 Pyrrole-3-Carbamidine 已被分离并鉴定为 Nierembergia Hippomanica 的致死成分.
DOI:10.1016/s0031-9422(00)84810-4

海关参考信息

专利信息


专利号:US-6683189-B1
优先权日:1996-02-26
标 题 :Method for the synthesis of pyrrole and imidazole carboxamides on a solid support
发明人:DERVAN PETER B; BAIRD ELDON
权利人:CALIFORNIA INST OF TECHN
摘要:The present invention describes a novel method for the solid phase synthesis of polyamides containing imidazole and pyrrole carboxamides. The polyamides are prepared on a solid support from aromatic carboxylic acids and aromatic amines with high stepwise coupling yields (>99%), providing milligram quantities of highly pure polyamides. The present invention also describes the synthesis of analogs of the natural products Netropsin and Distamycin A, two antiviral antibiotics. The present invention also describes a novel method for the solid phase synthesis of imidazole and pyrrole carboxamide polyamide-oligonucleotide conjugates. This methodology will greatly increase both the complexity and quantity of minor-groove binding polyamides and minor-groove binding polyamide-oligonucleotide conjugates which can be synthesized and tested.

专利号:WO-2024185775-A1
优先权日:2023-03-06
标 题:Long-chain alkenyloxy–substituted benzoyl derivative and oligonucleotide synthesis method using same
发明人:OKADA YOHEI; INANAGA KAZATO; SHOJI Yukiya; MIZUFUNE HIDEYA; SUDO TATSUYA; ADACHI Sota; HOSOI Kazushi
权利人:SPERA PHARMA INC; TOKYO UNIV OF AGRICULTURE AND TECHNOLOGY
摘要:The purpose of the present invention is to provide a novel pseudo–solid phase protecting group that can be used in liquid-phase oligonucleotide synthesis. The purpose of the present invention is also to provide an oligonucleotide synthesis method that uses a novel pseudo–solid phase protecting group. The present invention provides a compound represented by formula (1) (in which R represents a C14–60 alkenyl group, n represents 2 or 3, m represents 0 or 1, p represents 1 or 2, X represents C, N, O, or S, Y represents a single bond or B(CH 2 ) t * or may form a ring with X, and Z represents a single bond or (CH 2 ) s (s being an integer from 1 to 5)). The present invention also provides an oligonucleotide production method that uses the compound.

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-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.

专利号:US-7951905-B2
优先权日:2006-09-18
标 题 :Synthesis of carbohydrate-templated amino acids and methods of using same
发明人:SCHWEIZER FRANK; ZHANG KAIDONG; OWENS NEIL; ZHANEL GEORGE
权利人:UNIV MANITOBA
摘要:The present invention generally relates to tetrahydropyranyl-derivatized amino acids, their syntheses and their incorporation into peptides and peptidomimetics. The tetrahydropyran moiety constrains the side chain of an amino acid, thereby providing a molecule that may act as a sugar- or amino acid-mimetic as well as a scaffold for combinatorial synthesis.

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合成参考文献


摘要:M. Scrocco and R. Nicolaus, Atti accad. naz. Lincei, Rend. Classe sci. fis. mat. e nat. 22, 311 (1957); CA 52, 50i.
摘要:H. Rapoport and C. D. Willson, J. Org. Chem. 26, 1102 (1961).
摘要:M. M. T. Khan and A. E. Martell, J. Am. Chem. Soc. 91, 4668 (1969).
参考文献:10.1021/acs.jmedchem.0c00660
摘要:Mahy W, Patel M, Steadman D, Woodward HL, Atkinson BN, Svensson F, Willis NJ, Flint A, Papatheodorou D, Zhao Y, Vecchia L, Ruza RR, Hillier J, Frew S, Monaghan A, Costa A, Bictash M, Walter MW, Jones EY, Fish PV. Screening of a Custom-Designed Acid Fragment Library Identifies 1-Phenylpyrroles and 1-Phenylpyrrolidines as Inhibitors of Notum Carboxylesterase Activity. J Med Chem. 2020 Sep 10;63(17):9464–83. doi: 10.1021/acs.jmedchem.0c00660.
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