CAS: 90905-33-2; 2-Methylpyrimidine-5-Carbaldehyde

该化合物是具有青米丁环结构特征的有机化合物,其结构为六人芳香环,含有1号位置和3号位置的两个氮原子. 该化合物的特征是2位置的一组甲基和5位置的甲酰胺功能组,有助于其反应和有机合成的潜在应用.该物质一般是无色的,可粉黄黄色液体或固体,视温度和纯度而定. 甲酰胺组的存在使其在各种药物和农用化学合成中成为多功能中间体.此外,2甲基胺-5-碳代苯丁可能会由于电离性氮和氧原子的特性而表现出极性特征,影响其极地溶剂的溶性.该物质的再活动可包括典型的碱性添加核嗜血反应,使其在形成更复杂的有机分子时有用.应当参考安全数据,以便处理和储存,作为任何化学物质.

结构式图片

相似化合物

5194-32-1 2239-83-0 5571-03-9

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上下游产品

CAS号124-42-5 乙脒盐酸盐 | CAS号79-08-3 溴乙酸 | CAS号68-12-2 N,N-二甲基甲酰胺 | CAS号2009-81-6 [3-(dimethylami... | CAS号1071435-99-8 1-(2-甲基嘧啶-5-基)乙胺 | CAS号2239-83-0 2-甲基-5-嘧啶甲醇

合成工艺路线路线简述

  • 14874-70-5 + 45084-94-4 + 124-42-5 = 90905-33-2
    反应条件:1.1 Reagents: Sodium Ethoxide Solvents: Ethanol; 4 H,Reflux
    标题:Physical And Chemical Rationalization For Asymmetric Amplification In Autocatalytic Reactions
    作者:Buono,Frederic G.; Iwamura,Hiroshi; Blackmond,Donna G.
    参考文献:Angewandte Chemie 日期:2004 卷标:43(16) 页码:2099-2103]

    14874-70-5 + 45084-94-4 + 124-42-5 = 90905-33-2
    反应条件:1.1 Reagents: Sodium Ethoxide Solvents: Ethanol; Rt; 3 H,Reflux
    标题:Nonpeptide αvβ3 Antagonists. Part 11: Discovery And Preclinical Evaluation Of Potent αvβ3 Antagonists For The Prevention And Treatment Of Osteoporosis
    作者:Coleman,Paul J.; Brashear,Karen M.; Askew,Ben C.; Hutchinson,John H.; Mcvean,Carol A.; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2004 卷标:47(20) 页码:4829-4837]

    79-08-3 + 143-37-3 = 90905-33-2
    反应条件:1.1 Reagents: Phosphorus Oxychloride Solvents: Dimethylformamide; 6 H,90 °C1.2 Reagents: Sodium Tetrafluoroborate1.3 Reagents: Sodium Ethoxide Solvents: Ethanol; 3 H,Reflux
    标题:The Effect Of Carbon Nanotubes On Chiral Chemical Reactions
    作者:Rance,Graham A.; Miners,Scott A.; Chamberlain,Thomas W.; Khlobystov,Andrei N.
    参考文献:Chemical Physics Letters 日期:2013 卷标:557 页码:10-14
📜盐酸乙脒,2-Dimethylaminomethylene-1,3-Bis(Dimethylimmonio)Propane Bistetrafluoroborate置于sodium体系中,用 乙醇 作为反应溶剂,化学反应 5.0H,以10 G的收率获得产物2-甲基-5-嘧啶甲醛
参考文献:Benzamides
标题:Benzamides
摘要:本发明涉及含有抑制p2X7受体的苯甲酰胺类化合物.

海关参考信息

专利信息


专利号:US-2024309003-A1
优先权日:2021-05-04
标题 :Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
发明人:HOUZE JONATHAN B; BOS MAXENCE; MANCUSO JOHN; FRANZONI IVAN; PANDYA BHAUMIK; KAPLAN ALAN
权利人:VIGIL NEUROSCIENCE INC
摘要:The present disclosure provides compounds of Formula I, useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 (“TREM2â€?). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula I.

专利号:US-12428425-B2
优先权日:2020-05-04
标 题:Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
发明人:CZABANIUK LARA C; HOPPER TIMOTHY; HOUZE JONATHAN B; PANTELEEV JANE; RESCOURIO GWENAELLA; SANTORA VINCENT; WANG HAOXUAN; WHITE RYAN D; WONG ALICE R; WU YONGWEI; BOS MAXENCE; MANCUSO JOHN; FRANZONI IVAN
权利人:AMGEN INC; VIGIL NEUROSCIENCE INC
摘要:The present disclosure provides compounds of Formula I, useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 (“TREM2â€?).This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula I.

专利号:US-6764842-B2
优先权日:2001-03-28
标题 :Enantioselective bioreduction for the preparation of integrin receptor antagonist intermediates
发明人:STURR MICHAEL G; BOYD RUSSELL FIELDON; GBEWONYO KODZO; NTI-GYABAAH JOSEPH; POLLARD DAVID J; MCWILLIAMS JAMES CHRISTOPHER; TELARI KATHLEEN A
权利人:MERCK & CO INC
摘要:The present invention relates to a novel enantioselective bioreduction using a yeast microorganism for the preparation of the chiral allylic alcohols of structural formula I (R is hydrogen or methyl) which are useful in the asymmetric synthesis of integrin αvβ 3 receptor antagonists.

专利号:US-6410526-B1
优先权日:1999-06-02
标题 :αv integrin receptor antagonists
发明人:DUGGAN MARK E; HARTMAN GEORGE D; MEISSNER ROBERT S; PERKINS JAMES J
权利人:MERCK & CO INC
摘要:The present invention relates to novel nonanoic acid derivatives, their synthesis, and their use as alphav integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors alphavbeta3 and alphavbeta5 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, inflammatory arthritis, viral disease, cancer, and metastatic tumor growth.

专利号:US-6413955-B1
优先权日:1999-10-04
标 题:Integrin receptor antagonists
发明人:ASKEW BEN C; SMITH GARRY R
权利人:MERCK & CO INC
摘要:The present invention relates to compounds and derivatives thereof, their synthesis, and their use as vitronectin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors αvβ3 and/or αvβ5 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammatory arthritis, cancer, and metastatic tumor growth.

专利号:US-9428490-B2
优先权日:2011-07-29
标 题 :Nuclear transport modulators and uses thereof
发明人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD
权利人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD; KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to nuclear transport modulators, e.g CRM1 inhibitors, and more particularly to a compound represented by formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g, in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.

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合成参考文献


参考文献:10.1007/978-3-540-76886-9_10
摘要:Meierhenrich U. Accelerating the Carousel: Amplification Mechanisms. 2008. In: Advances in Astrobiology and Biogeophysics.
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