CAS: 62732-44-9; 2,3,5,6,7,8-Hexahydro-1H-Cyclopenta[b]Quinolin-9-Amine

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    📜1',5',6',7'-四氢螺[环己烷-1,2'-环戊二烯并[d]嘧啶]-4(3'H)-酮置于三氯氧磷体系中,用 甲苯 作为反应溶剂,化学反应 24.0H,以79%的收率获得产物2,3,5,6,7,8-六氢-1H-环戊并[b]喹啉-9-胺
    参考文献:Recyclization Of 2,2-Disubstituted 4(3H)-Oxo-And 4-Chloro-1,2-Dihydropyrimidines To 4-Aminopyridine Derivatives
    标题:Recyclization Of 2,2-Disubstituted 4(3H)-Oxo-And 4-Chloro-1,2-Dihydropyrimidines To 4-Aminopyridine Derivatives
    摘要:
    DOI:10.1007/bf00512825

    海关参考信息

    专利信息


    专利号:US-8063062-B2
    优先权日:2006-12-20
    标 题 :Compounds with a combination of cannabinoid-CB1 antagonism and acetylcholinesterase inhibition
    发明人:LANGE JOSEPHUS H M; KRUSE CORNELIS G; SHADID BELAL
    权利人:LANGE JOSEPHUS H M; KRUSE CORNELIS G; SHADID BELAL; SOLVAY PHARM BV
    摘要:Embodiments of this invention relate to compounds having a combination of cannabinoid-CB 1 antagonism and cholinesterase inhibition, to pharmaceutical compositions comprising these compounds, to methods for preparing these compounds, methods for preparing novel intermediates useful for the synthesis of these compounds, and methods for preparing compositions comprising these compounds. The invention also relates to methods of treating Alzheimer's disease, cognitive disorders, memory disorders, dementia, attention deficit disorder, traumatic brain injury, drug dependence, addiction or substance abuse by administering a pharmaceutical composition comprising these compounds to a patient in need thereof. A compound with a combination of cannabinoid-CB 1 antagonism and cholinesterase inhibition is a compound of formula (1) n nwherein the symbols have the meanings given in the specification.

    专利号:EP-2091939-B1
    优先权日:2006-12-20
    标 题 :Compounds with a combination of cannabinoid-cb1 antagonism and acetylcholinesterase inhibition
    发明人:LANGE JOSEPHUS H M; KRUSE CORNELIS G; SHADID BELAL
    权利人:ABBOTT HEALTHCARE PRODUCTS BV
    摘要:Thisinvention concerns compounds with a combination of cannabinoid-CB1antagonism and cholinesterase inhibition, to pharmaceutical compositions containing these compounds, to methods for preparing the compounds, methods for preparing novel intermediates useful for their synthesis, and methods for preparing compositions. The invention also relates to the uses of such compounds and compositions, particularly for treating Alzheimer's disease, cognitive disorders, memory disorders, dementia, attention deficits, traumatic brain injury, drug dependence, addiction and substance abuse. In particular the invention relates to compounds of the general Formula (1) wherein the symbols have the meanings given in the specification.

    专利号:US-2014315720-A1
    优先权日:2012-10-24
    标 题 :Polysaccharide ester microspheres and methods and articles relating thereto
    发明人:FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
    权利人:CELANESE ACETATE LLC
    摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Chernus VP, Vanchakova NP, Sivkova SK, Sivkov AS, Gorenkov RV. Ipidacrine in combination therapy regimens of functional constipation. Ter Arkh. 2018 Dec 30;90(12):48-55. doi: 10.26442/00403660.2018.12.000008.

    合成参考文献


    摘要:Pharmaceutical Chemistry Journal, 11(184), 1977
    摘要:Pharmaceutical Chemistry Journal, 23(709), 1989
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