CAS: 18202-73-8; Pivalimidamide Hydrochloride

该化合物是一种高纯度的化学化合物,主要用于有机合成和制药研究,其稳定的中间体结构以α-碳的二甲基替代为特征,增强了其作为三环化合物和中间体的构件的活性.盐的盐状提高了溶解性和水溶剂或极地溶剂系统中的处理能力.该化合物因其一贯质量,低杂质特征和适合核循环生物添加或凝聚反应而特别受重视.它作为发展生物活性分子(包括酶抑制剂和农用化学品)的关键前体,建议在无水条件下适当储存以保持稳定性.

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合成工艺路线路线简述

    📜三甲基乙腈置于盐酸,氨体系中,用 甲醇 用作溶剂,化学反应 3.0H,反应生成2,2-二甲基丙亚胺盐酸
    参考文献:胍的合成:As作为胍基化剂的用途
    标题:胍的合成:As作为胍基化剂的用途
    摘要:据报道of可用于胍的串联或一锅合成.胍是通过将易得的稳定stable稳定氧化成碳二亚胺,然后与胺进行原位反应而获得的.该方案可以在绿色溶剂(碳酸二甲酯)中,在温和的反应条件下(30oc)执行.胺的范围很广,包括位阻胺,对氧化敏感的胺和手性胺.提供了合成无环和环状胍的实例.由氧化剂[ N-(p可以高产率地分离出[甲苯磺酰基]亚氨基](2-丙氧基苯基)碘烷(2-Prophints),从而使高价碘试剂的再生成为可能.合成方法与最新技术相比,其实用性和绿色性通过抗高血压药物pinacidil的新途径得以证明.新路线的过程质量强度(pmi)仅是经典路线的24%.
    Doi:10.1002/adsc.201501146

    专利信息


    专利号:US-7897762-B2
    优先权日:2006-09-14
    标 题:Kinase inhibitors useful for the treatment of proliferative diseases
    发明人:FLYNN DANIEL L; PETILLO PETER A; KAUFMAN MICHAEL D; PATT WILLIAM C
    权利人:DECIPHERA PHARMACEUTICALS LLC
    摘要:The present invention relates to novel kinase inhibitors and modulator compounds useful for the treatment of various diseases. More particularly, the invention is concerned with such compounds, kinase/compound adducts, methods of treating diseases, and methods of synthesis of the compounds. Preferably, the compounds are useful for the modulation of kinase activity of Raf kinases and disease polymorphs thereof. Compounds of the present invention find utility in the treatment of mammalian cancers and especially human cancers including but not limited to malignant melanoma, colorectal cancer, ovarian cancer, papillary thyroid carcinoma, non small cell lung cancer, and mesothelioma. Compounds of the present invention also find utility in the treatment of rheumatoid arthritis and retinopathies including diabetic retinal neuropathy and macular degeneration.

    专利号:US-9018387-B2
    优先权日:2010-06-11
    标 题:Complexes of imidazole ligands
    发明人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; LEI XINJIAN; SPENCE DANIEL P; IVANOV SERGEI VLADIMIROVICH; BAILEY III WADE HAMPTON
    权利人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; LEI XINJIAN; SPENCE DANIEL P; IVANOV SERGEI VLADIMIROVICH; BAILEY III WADE HAMPTON; AIR PROD & CHEM
    摘要:Metal imidazolate complexes are described where imidazoles ligands functionalized with bulky groups and their anionic counterpart, i.e., imidazolates are described. Compounds comprising one or more such polyalkylated imidazolate anions coordinated to a metal or more than one metal, selected from the group consisting of alkali metals, transition metals, lanthanide metals, actinide metals, main group metals, including the chalcogenides, are contemplated. Alternatively, multiple different imidazole anions, in addition to other different anions, can be coordinated to metals to make new complexes. The synthesis of novel compounds and their use to form thin metal containing films is also contemplated.

    专利号:US-8188113-B2
    优先权日:2006-09-14
    标 题 :Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
    发明人:FLYNN DANIEL L; PETILLO PETER A; KAUFMAN MICHAEL D; PATT WILLIAM C
    权利人:FLYNN DANIEL L; PETILLO PETER A; KAUFMAN MICHAEL D; PATT WILLIAM C; DECIPHERA PHARMACEUTICALS INC
    摘要:The present invention relates to novel dihydropyridopyrimidinyl, dihydronaphthyridinyl, and related compounds which are kinase inhibitors and modulator useful for the treatment of various diseases. More particularly, the invention is concerned with such compounds, kinase/compound adducts, methods of treating diseases, and methods of synthesis of the compounds. Preferably, the compounds are useful for the modulation of kinase activity of Raf kinases and disease polymorphs thereof. Compounds of the present invention find utility in the treatment of mammalian cancers and especially human cancers including but not limited to malignant melanoma, colorectal cancer, ovarian cancer, papillary thyroid carcinoma, non small cell lung cancer, and mesothelioma. Compounds of the present invention also find utility in the treatment of rheumatoid arthritis and retinopathies including diabetic retinal neuropathy and macular degeneration.

    专利号:US-8703103-B2
    优先权日:2010-02-05
    标题 :Volatile imidazoles and group 2 imidazole based metal precursors
    发明人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; KIM MOO-SUNG
    权利人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; KIM MOO-SUNG; AIR PROD & CHEM
    摘要:Sterically hindered imidazole ligands are described, along with their synthesis, which are capable of coordinating to Group 2 metals, such as: calcium, magnesium, strontium, in an eta-5 coordination mode which permits the formation of monomeric or dimeric volatile complexes. n A compound comprising one or more polysubstituted imidazolate anions coordinated to a metal selected from the group consisting of barium, strontium, magnesium, radium or calcium or mixtures thereof. Alternatively, one anion can be substituted with and a second non-imidazolate anion. n Synthesis of the novel compounds and their use to form BST films is also contemplated.

    专利号:TW-572896-B
    优先权日:2000-05-26
    标 题:Process for the synthesis of amine ethers from secondary amino oxides

    专利号:TW-200811122-A
    优先权日:2006-03-27
    标题:A convergent process for the synthesis of taxane derivatives

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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


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 188.
    摘要:Xiao, X., Science of Synthesis: Knowledge Updates, (2023) 2, 205.
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