CAS: 41789-95-1; 1-(3-Methoxyphenyl)-N-Methylmethanamine

该化合物是一种二类甲胺衍生物,具有甲基代氧苯基环.该化合物因其结构多功能性,作为更复杂的分子的构件,对有机合成和制药研究具有兴趣.甲氧基混合物组会提高电子密度,影响电除尘替代或金属催化联动反应中的再活动.其次类安咪功能允许进一步衍生,如再降解或串联.该化合物通常用于生物活性分子的开发,包括潜在的离子体或药物发现中间体.建议由于对氧化的潜在敏感性,在惰性条件下进行妥善处理.常见有机溶剂中易溶性,便于其在合成应用中使用.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

methylamine hydr°Chloride 3-methoxy-benzaldehyde methylamine 1-bromomethyl-3-methoxybenzene (3-methoxy-benzyl)-(4-methoxy-benzyl)-methyl-amine 2-[(3-Methoxy-benzyl)-methyl-amino]-6,6-dimethyl-4-oxo-cyclohex-2-enecarbonitrile N-methyl-3-methoxybenzylammonium chloride N-nitroso-N-(3-methoxybenzyl)methylamine

合成工艺路线路线简述

    3-甲氧基溴苄置于palladium On Activated Charcoal 氢气体系中,用 四氢呋喃,甲苯 作为反应溶剂,化学反应生成 N-甲基-3-甲氧基苄胺
    参考文献:Valentini,Piero; Rampa,Angela; Bisi,Alessandra,Medicinal Chemistry Research,1995,Vol. 5,# 4,P. 255-264
    标题:Valentini,Piero; Rampa,Angela; Bisi,Alessandra,Medicinal Chemistry Research,1995,Vol. 5,# 4,P. 255-264

    海关参考信息

    专利信息


    专利号:WO-2011050245-A1
    优先权日:2009-10-23
    标 题:Bicyclic heteroaryls as kinase inhibitors
    发明人:FENG YANGBO; CHEN YEN TING; SESSIONS HAMPTON; MISHRA JITENDRA K; CHOWDHURY SARWAT; YIN YAN; LOGRASSO PHILIP; LUO JUN-LI; BANNISTER THOMAS; SCHROETER THOMAS
    权利人:FENG YANGBO; CHEN YEN TING; SESSIONS HAMPTON; MISHRA JITENDRA K; CHOWDHURY SARWAT; YIN YAN; LOGRASSO PHILIP; LUO JUN-LI; BANNISTER THOMAS; SCHROETER THOMAS
    摘要:The invention is directed to heteroaryl compounds useful as inhibitors of various kinase enzymes. In various embodiments, the invention provides a heteroaryl compound having inhibitory bioactivity with respect to a Rho kinase, an AKT kinase, a p70S6K kinase, a LIM kinase, an IKK kinase, a Flt kinase, an Aurora kinase, or a Src kinase, or any combination thereof. Compounds of the invention include bicyclic heteroaryl compounds of formula (I), which can contain a bridging nitrogen atom at a ring junction. The invention further provides methods of synthesis of compounds of the invention, pharmaceutical compositions, pharmaceutical combinations, and methods of treatment of malconditions using compounds of the invention.

    专利号:US-10766863-B2
    优先权日:2014-11-17
    标 题 :Monocarboxylate transport modulators and uses thereof
    发明人:SANDANAYAKA VINCENT; WU QIONG
    权利人:NIROGYONE THERAPEUTICS INC
    摘要:The invention generally relates to the field of monocarboxylate transport modulators, e.g., monocarboxylate transport inhibitors, and more particularly to new substituted-quinolone compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in treating, modulating, forestalling and/or reducing physiological conditions associated with monocarboxylate transport activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, obesity, diabetes, cardiovascular diseases, tissue and organ transplant rejection, and malaria.

    专利号:US-2008194590-A1
    优先权日:2005-03-28
    标 题:4-Piperazinylthieno [2,3-D] Pyrimidine Compounds as Platelet Aggregation Inhibitors
    发明人:ENNIS MICHAEL DALTON; KORTUM STEVEN WADE; TENBRINK RUTH ELIZABETH
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula (I) wherein A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 , A 8 , X 4 , X 6 , X 2k , R 2l , R 4 , R 5 , and R 6 are as defined in the detailed description of the invention. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
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    合成参考文献


    参考文献:10.1055/s-0035-1561767
    摘要:Synthesis of (+)-BMS-820836. Synfacts. 2016 Mar 15;12(04):0338. doi: 10.1055/s-0035-1561767.
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