CAS: 1069-72-3; 2-Bromo-N,N-Diethylethylamine Hydrobromide

该化合物是一种化学化合物,其结构特征包括一个与氮原子相连的溴原子,该化学原子又与两个乙基组和一个乙基组相连接;该化合物是一种四硝基铵盐,通常以白晶状固体的形式出现;在水和极有机溶剂中溶解,使其在各种化学应用中有用;溴原子的存在有助于其再活性,使其得以参与核生殖替代反应;作为氢溴化盐,该化合物是由碱与水溴酸的反应形成,该盐可增强该物质的稳定性和溶解性;该化合物经常用于有机合成,可作为生产药品或其他有机化合物的中间体;在处理该物质时,应注意安全防范,因为如果浸入或吸入,可能会对健康造成危害,因此应使用适当的个人防护设备.

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CAS号100-37-8 二乙氨基乙醇 | CAS号589-32-2 四乙基胱胺-13C4 | CAS号104-79-0 N,N-二乙基-N'-甲基乙二胺 | CAS号125906-52-7 N,N-diethyl-2-q... | CAS号109-89-7 二乙胺 | CAS号84434-83-3 N-[(4-chlorophe... | CAS号5392-81-4 2-溴-N,N-二乙基乙胺氢溴酸 | CAS号5427-35-0 N-(4-chlorophen...

合成工艺路线路线简述

  • 合成目标产物 2-Bromo-N,N-Diethylethylamine Hydrobromide 主要起始原料 Diethylaminoethanol
  • (文献来源)合成步骤主要原料 Diethylaminoethanol
📜二乙氨基乙醇置于三溴化磷体系中,用 甲苯 用作溶剂,化学反应生成2-二乙氨基-1-溴乙烷氢溴酸盐
参考文献:一种盐酸胺碘酮的制备方法
标题:一种盐酸胺碘酮的制备方法
摘要:本发明公开了一种盐酸胺碘酮的制备方法,具体步骤为:首先以2‑丁基苯并呋喃为起始原料,与对甲氧基苯甲酰氯发生傅克酰基化反应和去甲基反应,得到2‑丁基‑3‑(4‑羟基苯甲酰基)苯并呋喃,然后2‑丁基‑3‑(4‑羟基苯甲酰基)苯并呋喃与碘发生碘代反应,得到2‑丁基‑3‑(3,5‑二碘‑4‑羟基苯甲酰基)苯并呋喃,最后2‑丁基‑3‑(3,5‑二碘‑4‑羟基苯甲酰基)苯并呋喃与2‑二乙氨基溴乙烷氢溴酸盐发生缩合反应,调节ph浓缩析晶重结晶,即得盐酸胺碘酮.本发明缩合反应采用2‑二乙氨基溴乙烷氢溴酸盐,规避了起始原料不易购买的问题,同时提高了反应效率,成品的质量也有所提高,并且制备工艺简单,操作方便,生产周期更短,更适合于工业化生产.

专利信息


专利号:US-2024409495-A1
优先权日:2021-10-20
标 题 :Process for the preparation of 2,7-dihydroxy-9-fluorenone useful for the synthesis of tilorone and its salts
发明人:JAISANKAR PARASURAMAN; DEB INDUBHUSAN; BHATTACHARJEE PINAKI
权利人:COUNCIL SCIENT IND RES
摘要:Methods involving preparation of building blocks of 2,7-dihydroxy-9-fluorenone toward the synthesis of tilorone dihydrochloride salt and other salts (bromide, iodide, fluoride, citrate, oxalate, maleate, phosphate, tartrate, triflate, trifluoroacetate, tetrafluoroborate) of tilorone, and an efficient, safe, cost effective method for the preparation of 2,7-bis-[2-(diethylamino)ethoxy]-fluorenone-9 and its various salts are developed. The methods involve oxygenation of fluorene, nitration of fluorenone, followed by reduction and diazotization toward the formation of 2,7-dihydroxy-9-fluorenone, which is the key intermediate for the formation of 2,7-bis-[2-(diethylamino)ethoxy]-9-fluorenone-dihydrochloride (Tilorone dihydrochloride) and other tilorone salts. The synthesis method has relatively simple operation, mild reaction conditions, high yield, and simple process with yields of 80-97%. Subsequent product purification of this method uses filtration and crystallization methods, avoiding the existing methods of column chromatography. Therefore, the research of its synthetic method being with a wide range of applications from the drug development and material synthesis point of view.

专利号:WO-2023067624-A1
优先权日:2021-10-20
标 题 :A process for the preparation of 2,7-dihydroxy-9-fluorenone useful for the synthesis of tilorone and its salts

专利号:CN-118175999-A
优先权日:2021-10-20
标题 :Process for the preparation of 2, 7-dihydroxy-9-fluorenone useful for the synthesis of telulone and its salts

专利号:CA-3235754-A1
优先权日:2021-10-20
标 题 :A process for the preparation of 2,7-dihydroxy-9-fluorenone useful for the synthesis of tilorone and its salts

专利号:EP-0617288-B1
优先权日:1993-03-19
标题 :Long emission wavelength chemiluminescent compounds and their use in test assays
发明人:LAW SAY-JONG; JIANG QINGPING; FISCHER WALTER; UNGER JOHN T; KRODEL ELIZABETH K
权利人:NOVARTIS AG; BAYER AG
摘要:An assay method incorporating at least two different chemiluminescent compounds for detection and/or quantitation of at least two substances in a test sample is described. The synthesis of chemiluminescent reagents or conjugates for use in such methods as well as kits incorporating such reagents are also disclosed. The assays have particular application in the field of clinical diagnostics.

专利号:US-7189749-B2
优先权日:1999-06-25
标 题 :Substituted phenoxyacetic acids
发明人:VAN ZANDT MICHAEL C
权利人:INST FOR PHARM DISCOVERY INC
摘要:Disclosed are substituted phenoxyacetic acids useful in the treatment of chronic complications arising from diabetes mellitus. Also disclosed are pharmaceutical compositions containing the compounds, alone or in combination with other therapeutic agents, and methods of treatment employing the compounds and pharmaceutical compositions, as well as methods for their synthesis.

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主要参考文献

[参考文献]: Luca Boselli, Et Al. Synthesis, Structures, And Selective Toxicity To Cancer Cells Of Gold(I) Complexes Involving N-Heterocyclic Carbene Ligands. Eur J Med Chem. 2014 Oct 6:85:87-94.

合成参考文献


参考文献:10.1007/s11164-015-2086-2
摘要:Senthilkumar N, Ravichandran YD, Kumar KM, Ramaiah S. Synthesis of a new series of pyrimidine derivatives: exploration of anti-proliferative activity on EAT cells and molecular docking. Research on Chemical Intermediates. 2015 May 21;42(2):1295–313. doi: 10.1007/s11164-015-2086-2.
参考文献:10.1007/s10870-009-9554-8
摘要:Bentivoglio G, Schwärzler A, Wurst K, Kahlenberg V, Nauer G, Bonn G, Schottenberger H, Laus G. Hydrogen Bonding in the Crystal Structures of New Imidazolium Triflimide Protic Ionic Liquids. Journal of Chemical Crystallography. 2009 Mar 20;39(9):662–8. doi: 10.1007/s10870-009-9554-8.
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