CAS: 107-90-4; Butyrimidamide

该化合物是多功能的米介质化合物, 其应用在有机合成和制药研究中. 它的结构由四碳链组成, 由一个米介质集团终止, 使得它能够用作三环化合物和生物活性分子的构件. 水介质功能提供了很强的核循环和基本特性, 便利了凝聚和循环等反应. 丁胺化因其在温和条件下的稳定性和再活性而特别受到重视, 使其适合受控合成工艺. 它作为准备伊米卓, 皮米丁和其他含氮的乙型循环的前体, 有助于其在医药化学和材料科学中的用途 .

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CAS号109-74-0 正丁腈 | CAS号924-74-3 O-ethyl butanet...

合成工艺路线路线简述

    📜丁腈置于氨,溴化铵体系中,化学反应生成丁脒
    参考文献:Preparation Of Amidine Salts By Reaction Of Nitriles With Ammonium Salts In The Presence Of Ammonia
    标题:Preparation Of Amidine Salts By Reaction Of Nitriles With Ammonium Salts In The Presence Of Ammonia
    摘要:
    Doi:10.1021/jo01051A033

    专利信息


    专利号:US-2004092003-A1
    优先权日:1997-03-19
    标题:Multifunctional ceramic particles as solid supports for solid phase and combinatorial solid phase synthesis
    发明人:BOSCHETTI EGISTO; KOCIS PETR
    权利人:INVITROGEN CORP
    摘要:Inert, thermally and mechanically stable porous ceramic solid phase supports for use in solid phase synthesis of molecules wherein the porous ceramic solid supports can be used under a wide variety of reaction conditions and in synthesis methods, including but not limited to organic, regular, multiple parallel, or combinatorial organic synthesis on a solid phase. Methods of using the porous ceramic solid supports for solid phase synthesis of molecules, for solid phase synthesis of polypeptides or peptidomimetics, for generating combinatorial libraries of linkers, and for combinatorial synthesis of compounds, including small molecules and aromatic and heteroaromatic compounds.

    专利号:US-2003180804-A1
    优先权日:2001-10-29
    标题:Solid phase synthesis of chemical libraries
    发明人:PRYOR KENT E; LEWIS RONALD D; BROWN JASON W
    权利人:CORVAS INT INC
    摘要:The present invention provides compounds and compound libraries that are useful as protease modulators. The compounds and compound libraries are preferably made using the methods of the present invention which utilize peptide synthesis and combinatorial chemistry methods on a solid phase.

    专利号:US-5712407-A
    优先权日:1997-01-14
    标题 :Method for the preparation of alpha-chlorinated chloroformates
    发明人:KREUTZBERGER CHARLES B; ESWARAKRISHNAN SEETHA; DAMLE SURESH B
    权利人:PPG INDUSTRIES INC
    摘要:Novel catalysts for the synthesis of a alpha-chlorinated chloroformate from an aldehyde and phosgene are described. The catalysts include alkyl substituted guanidines, hexasubstituted guanidinium chlorides, substituted biguanidinium chloride, phenyldialkyliminiumtetraalkylguanidinium chloride, dialkylimidazolinium tetraalkylguanidinium chloride, phenyltetraalkylamidinium chloride and N,N-dialkyl-N'-alkylpyrrolidinium chloride.

    专利号:US-4443629-A
    优先权日:1981-07-03
    标 题 :Preparation of hydrazidines
    发明人:BONSE GERHARD; SCHMIDT THOMAS
    权利人:BAYER AG
    摘要:A one-step process for the preparation of hydrazidines of the general formula (I) in which R represents an optionally substituted alkyl group, an optionally substituted cycloalkyl group, an optionally substituted aryl group or an optionally substituted aralkyl group, or their acid addition salts, in high yield, comprises reacting appropriate amidines or their acid addition salts with hydrazine in solvents at reduced pressure and at temperatures between -80 DEG C. and +100 DEG C., the reaction being effected in the presence of water present in the solvent and/or in the hydrazine by employing it as hydrazine hydrate. The hydrazidines of formula (I) and their salts are valuable intermediates in heterocyclic chemistry, for example for the synthesis of herbicidally active as-triazinones.

    专利号:US-12286405-B2
    优先权日:2019-05-17
    标题 :Scalable synthesis of dual-target inhibitor of cannabinoid-1 receptor and inducible nitric oxide synthase
    发明人:ALIMARDANOV ASAF RAGIM; HUANG JUNFENG
    权利人:US HEALTH
    摘要:A process for the preparation of racemic and optically active (1E,NE)-N-(1-aminoethylidene)-3-(4-chlorophenyl)-4-phenyl-N′-((4-(trifluoromethyl)phenyl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide in high enantiomerical purity is provided.

    专利号:US-6040440-A
    优先权日:1998-03-06
    标题:Hypophosphite deoxygenation reactions in the synthesis of erythromycin derivatives
    发明人:GRAHAM ALEXANDRA E; THOMAS ALBERT V; YANG RACHEL R P
    权利人:ABBOTT LAB
    摘要:A process for the preparation of 4''-deoxyerythromycins, having the formula: wherein R is H or OH, R1 is H or loweralkyl, and R2 is H or CH3 by treatment of the starting material, 2'-O-acetyl-4''-imidazolylthiocarbamoyl-erythromycin, with a hypophosphite reagent, in a water-miscible protic solvent optionally comprising a phase transfer agent. In a preferred embodiment, the water-miscible solvent is an alcohol and the starting material is reacted with sodium hypophosphite, ACVA and tetra-n-butylammonium hydroxide.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 180.
    摘要:Kang, F.-A.; Yang, S.-M., Science of Synthesis Knowledge Updates, (2015) 2, 185.
    参考文献:10.1007/bf03033561
    摘要:Sapcanin A, Sofic E, Tahirovic I, Salkovic-Petrisic M, Hoyer S, Riederer P. Antioxidant capacity in rat brain after intracerebroventricular treatment with streptozotocin and alloxan--a preliminary study. Neurotox Res. 2008 Apr;13(2):97–104. doi: 10.1007/bf03033561.
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