CAS: 2217-41-6; 1-Amino-5,6,7,8-Tetrahydronaphthalene

该化合物是一种有机化合物,其特点是双环结构,由部分饱和的环环环系统组成;该化合物具有一个有矿功能的组,使其成为氯化萘的衍生物;该化合物一般是无色的,根据纯度和温度,淡黄色液体或固态是无色的;该矿组的存在具有基本特性,允许其参与各种化学反应,例如核循环替代和混合反应;该化合物经常用于染料,药品和其他有机化合物合成;此外,5,6,7,7,8-四氢-1-甲苯胺在有机溶剂中可能表现出中等溶解性,而其在水中的溶解性一般较低;应当参考安全数据,因为吸入或摄取会给健康带来风险,因此应在实验室环境中采取适当的防范措施.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

tetralin 1-Nitronaphthalene 6-nitrotetralin 5-nitro-1,2,3,4-tetrahydronaphthalene N-(5,6,7,8-tetrahydro-[1]naphthyl)-phthalamic acidN-(5,6,7,8-tetrahydro-[1]naphthyl)-phthalamic acid N-phenyl-N'-(5,6,7,8-tetrahydro-[1]naphthyl)-ureaN-phenyl-N'-(5,6,7,8-tetrahydro-[1]naphthyl)-urea N-phenyl-N'-(5,6,7,8-tetrahydro-[1]naphthyl)-thioureaN-phenyl-N'-(5,6,7,8-tetrahydro-[1]naphthyl)-thiourea 1-(Chloroacetamido)-5,6,7,8-tetrahydronaphthalin

合成工艺路线路线简述

  • 合成目标产物 5,6,7,8-Tetrahydro-1-Naphthylamine 主要起始原料 1,8-Diaminonaphthalene
  • (文献来源)合成步骤主要原料 1,8-Diaminonaphthalene
1,8-二氨基萘置于氢气体系中,用 甲醇 用作溶剂,150.0 °C,2.2 Mpa 条件下,反应 4.0H,以98.3%的收率获得1-氨基四氢化萘
参考文献:一种以1,8-二氨基萘为原料制备5,6,7,8-四氢-1-萘胺的方法
标题:一种以1,8-二氨基萘为原料制备5,6,7,8-四氢-1-萘胺的方法
摘要:本发明公开了一种以1,8‑二氨基萘为原料制备5,6,7,8‑四氢‑1‑萘胺的方法,所述的方法为:以1,8‑二氨基萘为原料,以雷尼镍为催化剂,以氢气为还原剂,在有机溶剂中,于氢气压力1.5~2.5Mpa,温度120~180oc的条件下反应2‑10小时,反应液过滤浓缩即制得5,6,7,8‑四氢‑1‑萘胺.本发明所述的合成方法操作简便安全,催化加氢是一种绿色合成方法,产品收率高,三废少.

海关参考信息

专利信息


专利号:US-2022281888-A1
优先权日:2019-09-25
标题:Bicyclic carboxylates as modulators of transporters and uses thereof
发明人:SANDANAYAKA VINCENT; GORECZNY GREGORY
权利人:NIROGY THERAPEUTICS INC
摘要:The present invention generally relates to the field of transporter modulators, e.g., monocarboxylate transporter inhibitors, and more particularly to new bicyclic enone carboxylate compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with monocarboxylate transporter activity such as in treating cancer and other neoplastic disorders, tissue and organ transplant rejection.

专利号:US-6531470-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

专利号:US-5916899-A
优先权日:1996-10-18
标 题:Isoquinoline derivatives and isoquinoline combinatorial libraries
发明人:KIELY JOHN S; GRIFFITH MICHAEL C
权利人:TREGA BIOSCIENCES INC
摘要:The present invention provides the synthesis of heterocyclic compounds based on the isoquinoline ring. More specifically, the invention provides novel isoquinolines as well as novel libraries comprised of many such compounds, and methods of synthesizing the libraries.

专利号:US-10458995-B2
优先权日:2016-03-25
标 题 :Combinatorial synthesis and biomarker development
发明人:MOOLA MURALIDHAR REDDY
权利人:MOOLA MURALIDHAR REDDY
摘要:Provided herein are methods, kits, and compositions for use in the diagnosis and treatment of diseases. Peptoids recognized by Alzheimers disease specific antibodies are identified.

专利号:US-2011098483-A1
优先权日:2008-03-27
标题 :Substituted Nitrogen Heterocycles and Synthesis and Uses Thereof
发明人:PETASIS NICOS A; MYSLINSKA MALGORZATA
权利人:UNIV SOUTHERN CALIFORNIA
摘要:The invention relates to a nitrogen heterocycle compound of formula 1: n n n n n n n n n n Also disclosed are a method of synthesizing the compound and use of the compound for treating various diseases and conditions.

专利号:US-6562844-B2
优先权日:1998-01-23
标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
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合成参考文献


摘要:Dai, X.; Shi, F., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 135.
摘要:Virchows Archiv fuer Pathologische, Anatomie und Physiologie, und fuer Klinische Medizin., 115(14), 1889
摘要:Fogel, M. S.; Shellnutt, Z. S.; Koide, K., Science of Synthesis: Dearomatizations, (2026) .
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