CAS: 485-64-3; (R)-((1S,2S,4S,5R)-5-Ethylquinuclidin-2-yl)(Quinolin-4-yl)Methanol

该化合物其独特的行动机制有助于其预防感染和促进伤口愈合的功效. 辛卡米迪因毒性低和与各种皮肤类型高度兼容而特别有利,因此它成为医疗和药物应用的适当选择.

结构式图片

相似化合物

485-65-4 5962-19-6 118-10-5

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号486-74-8 4-喹啉羧酸 | CAS号491-35-0 4-甲基喹啉 | CAS号612-11-3 3,4-二乙吡啶

合成工艺路线路线简述

    📜辛可尼丁置于palladium On Activated Charcoal 氢气体系中,用 甲醇 作为反应溶剂,化学反应 12.0H,以86%的收率获得产物(8Alpha,9R)-10,11-二氢脱氧辛可宁-9-醇
    参考文献:相转移催化的不对称酰基咪唑烷基化.
    标题:相转移催化的不对称酰基咪唑烷基化.
    摘要:在2-辛基吡啶鎓催化剂的相转移条件下,将2-酰基咪唑与烯丙基和苄基亲电子试剂在-40oc下以高收率和优异的对映选择性(79至> 99%ee)烷基化.酰基咪唑底物由溴乙酸经n-酰基吗啉加合物分三步制备.该催化剂以高纯度制备,可在温和条件下形成s产物(6-20小时),这与离子对机理相符.使用三氟甲磺酸甲酯和甲醇钠,经由二甲基酰基咪唑鎓中间体容易地将产物转化为有用的酯产物,而没有外消旋作用.该过程是有效的,直接的,并且适合于通过烯醇化中间体进行的其他亲电试剂和转化.
    DOI:10.1021/ol702197R

    海关参考信息

    专利信息


    专利号:US-9126995-B2
    优先权日:2011-11-08
    标题:Method for catalytic asymmetric synthesis of optically active isoxazoline compound and optically active isoxazoline compound
    发明人:TOYAMA KEN-ICHI; MORIYAMA YUJI; MATOBA KAZUTAKA; YAOSAKA MANABU; IKEDA EITATSU
    权利人:NISSAN CHEMICAL IND LTD
    摘要:There is provided a method for catalytic asymmetric synthesis of optically active isoxazoline compound and an optically active isoxazoline compound. A method for catalytic asymmetric synthesis of optically active isoxazoline compound of a formula (6) including reacting an α,β-unsaturated carbonyl compound of a formula (1) and a hydroxylamine in a solvent in the presence of a base by adding a chiral phase transfer catalyst. An optically active isoxazoline compound of a formula (13) that can be synthesized by the method.

    专利号:US-9593071-B2
    优先权日:2011-11-22
    标题 :Process for the preparation of gamma amino acids and intermediates used in said process
    发明人:ADAMO MAURO
    权利人:ROYAL COLLEGE SURGEONS IRELAND
    摘要:The invention relates to the preparation of gamma amino acids of formula (I) and pharmaceutically acceptable salts, solvates and prodrugs thereof, and to intermediates used for their preparation. (formula I) wherein R 1 is selected from an alkyl group, an alkenyl group, an alkynyl group and a cycloalkyl group, each of which may be optionally substituted and * denotes a chiral center. In particular, the present invention provides an efficient synthesis of (S)-pregabalin which is suitable for carrying out on an industrial scale.

    专利号:US-2014350261-A1
    优先权日:2011-11-08
    标 题 :Method for catalytic asymmetric synthesis of optically active isoxazoline compound, and optically active isoxazoline compound

    专利号:WO-2011138625-A1
    优先权日:2010-05-07
    标题 :Industrial process for the synthesis of ivabradine salts

    专利号:WO-2013069731-A1
    优先权日:2011-11-08
    标题 :Method for catalytic asymmetric synthesis of optically active isoxazoline compound, and optically active isoxazoline compound

    专利号:NL-9100854-A
    优先权日:1990-05-17
    标 题 :METHOD FOR PREPARING INTERMEDIATES USE FOR THE SYNTHESIS OF BENZODIAZEPINES.

    供应商参考报价(招募中)

    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

    主要参考文献


    1: Bartók M, Szabó PT, Bartók T, Szöllösi G. Identification of ethyl pyruvate and dihydrocinchonidine adducts by electrospray ionization mass spectrometry. Rapid Commun Mass Spectrom. 2000;14(6):509-14. doi: 10.1002/(SICI)1097-0231(20000331)14:6<509::AID-RCM902>3.0.CO;2-P. 5(14):2283-90. doi: 10.1039/b706546a. Epub 2007 Jun 13. 19(24):3743-8. doi: 10.1002/rcm.2252.

    合成参考文献


    摘要:Chemler, S. R.; Zabawa, T. P., Science of Synthesis, (2007) 20, 1216.
    摘要:Chemler, S. R.; Zabawa, T. P., Science of Synthesis, (2007) 20, 1217.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知