CAS: 66521-54-8; 3-(Dimethylamino)-1-(Pyridin-2-yl)Prop-2-En-1-One

该化合物是一种具有二甲基氨基替代物和丙烯基酰基的共聚酶系统,其结构可应用于合成化学,特别是作为三环化合物和药物的构件.富乙基甲基氨基电组可增强迈克尔添加物和循环反应的回弹性,而环则提供金属复合物的协调点.该化合物因其稳定性,定义明确的再活动性以及生物活性分子合成的效用而备受重视,通常用于学术和工业研究,以开发具有潜在药理活动的新型化学实体.

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123367-25-9 63285-43-8 112677-15-3

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2-acetylpyridine N,N-dimethyl-formamide dimethyl acetalN,N-dimethyl-formamide dimethyl acetal N,N-dimethylformamide diethyl diacetal N,N-dimethyl-formamide 2-(1H-pyrazol-3-yl)pyridine pyridin(+)-2-1-(1-Phenylethyl)-5-pyrazolylpyridin 4-(pyridin-2-yl)pyrimidine 2,2':6,2''-terpyridine

合成工艺路线路线简述

    📜2-乙酰基吡啶,N,N-二甲基甲酰胺二甲基缩醛 以 甲苯 作为反应溶剂,化学反应 12.0H,以98%的收率获得产物3-(二甲氨基)-1-(2-吡啶基)-2-丙烯-1-酮
    参考文献:铱(iii)光催化还原剂的合成,表征及应用
    标题:铱(iii)光催化还原剂的合成,表征及应用
    摘要:通式为[ir Iii(c ^ N)2(n ^ N)] +(c ^ N:环金属化苯基吡啶配体,N ^ N:中性的新型单阳离子铱(iii)光敏剂(ir-Pss)的合成描述了二齿配体.通过循环伏安法,Uv / Vis和光致发光光谱法和x射线分析检查获得的结构.测试了所有铱配合物作为光敏剂的能力,以促进从水中均匀催化的氢气反应生成.在[hnet 3] [hfe 3(co)11]作为减水催化剂(wrc)和三乙胺作为牺牲性还原剂(sr)的存在下,七个新的铱络合物表现出活性.[ir(6‐ Ipr-Bpy)(ppy)2] Pf 6(bpy:2,2'-联吡啶,Ppy:2-苯基吡啶)被证明是最有效的光敏剂.还对该复合物与其他基于铑,铂,钴和锰的wrc进行了测试.在所有情况下,都会发生大量的氢气逸出.从[hnet 3] [hfe 3(co)11]和三[3,5-双(三氟甲基)苯基]膦现场反应生成的ir-Ps的最大周转数为4550,Fe
    DOI:10.1002/chem.201100235

    海关参考信息

    专利信息


    专利号:US-5064963-A
    优先权日:1990-04-25
    标 题 :Process for the synthesis of n-(3-(1h-imidazol-1-yl)phenyl-4-(substituted)-2-pyrimidinamines
    发明人:DEAN WILLIAM D
    权利人:AMERICAN CYANAMID CO
    摘要:The invention provides a novel process for producing N-[3-(1H-imidazol-1-yl)phenyl]-4-(substituted)-2 pyrimidinamine compounds in which the substituent is a 2-pyridinyl, 3-pyrindinyl, 4-pyridinyl, 2-furanyl or 2-thienyl group. The process includes the steps of (1) reacting a 3-(1H-imidazol-1-yl)benzamine with cyanamide and a halogen acid while controlling the pH of the reaction between pH about 2 to abourt 3.5 and recovering a [3-(1H-imidazol-1-yl)phenyl] guanidine dihydrohalide and (2) reacting the [3-(1H-imidazol-1-yl)phenyl] guanidine dihydrohalide so recovered with an appropriately substituted 3-dimethylamino-1-(substituted)-2-propen-1-one and a base at a pH of from about 10.5 to about 11.5 and recovering the N-[3-(1H-imidazol-1-yl)phenyl-4-(substituted)-2-pyrimidamine compound so produced. The novel process provides improved yield and purity by adhering to the stated crucial pH ranges.

    专利号:EP-0453731-A2
    优先权日:1990-04-25
    标题 :Improved process for the synthesis of N-3-(1H-imidazol-1-yl)phenyl-4-(substituted)-2-pyrimidinamines

    专利号:HU-211774-B
    优先权日:1990-04-25
    标 题:Improved process for the synthesis of n-[3-(1h-imidazol-1-yl)phenyl]-4-substituted-2-pyrimidinamines

    专利号:EP-0453731-B1
    优先权日:1990-04-25
    标 题:Improved process for the synthesis of N-3-(1H-imidazol-1-yl)phenyl-4-(substituted)-2-pyrimidinamines

    专利号:EP-0453731-A3
    优先权日:1990-04-25
    标 题 :Improved process for the synthesis of n-3-(1h-imidazol-1-yl)phenyl-4-(substituted)-2-pyrimidinamines

    专利号:JP-H04225975-A
    优先权日:1990-04-25
    标题:Improved method for synthesis of N-[3-(1H-imidazol-1-yl)phenyl]-4-(substituted)-2-pyrimidinamine

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/s10593-023-03253-4
    摘要:Nikolaenkova EB, Shekhovtsov NA, Bushuev MB, Krivopalov VP. Synthesis of azinyl azolyl pyrimidines as new hybrid N,N,N-tridentate ligands for coordination chemistry. Chem Heterocycl Comp. 2023 Sep;59(9-10):672–84. doi: 10.1007/s10593-023-03253-4.
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