CAS: 2216-69-5; 1-Methoxynaphthalene

相似化合物

3900-49-0 10075-62-4 10075-63-5

上下游产品

CAS号90-15-3 1-萘酚 | CAS号77-78-1 硫酸二甲酯 | CAS号112183-02-5 4-methoxynaphth... | CAS号5961-55-7 4-甲氧基-1-萘甲腈 | CAS号67-56-1 甲醇 | CAS号90-11-9 1-溴代萘 | CAS号1201594-02-6 4-methoxynaphth... | CAS号412041-47-5 1,2-diethynyl-3... | CAS号124-41-4 甲醇钠 | CAS号5467-58-3 1-溴-4-甲氧基萘 | CAS号10465-20-0 1-Naphthalenebu... | CAS号119-64-2 1,2,3,4-四氢萘(THN) | CAS号1008-19-1 5-甲氧基-1,2,3,4-四氢萘 | CAS号66324-83-2 1,2,3,4-tetrahy... | CAS号3562-99-0 孟布酮 | CAS号4900-63-4 1-甲氧基-4-硝基萘 | CAS号605-69-6 马休黄 | CAS号5961-55-7 4-甲氧基-1-萘甲腈 | CAS号4900-62-3 1-methoxy-2-nit... | CAS号13041-62-8 4-甲氧基-1-萘甲酸

N,N-二甲基-1-萘胺 以 二氯甲烷,N,N-二甲基甲酰胺 用作溶剂,化学反应 3.0H,反应生成1-甲氧基萘
参考文献:从苯胺到芳醚:一种温和条件下的简便,高效且多功能的合成方法
标题:从苯胺到芳醚:一种温和条件下的简便,高效且多功能的合成方法
摘要:我们通过醇/酚(roh)与芳基铵盐(arnme反应开发了用于芳基醚的合成的简单且直接的方法3 +),它很容易从苯胺制备(arnr' 2,R'= H或me) .该反应在室温下顺利地且快速地进行(在几个小时内)在市售的碱,例如ko的存在吨卜或khmds,并具有相对于二者roh和arnr'宽的底物范围2.它具有可扩展性,并且与各种功能组兼容.
Doi:10.1002/anie.201712618

专利信息

专利号:US-2013338369-A1
优先权日:2011-03-07
标 题 :Process for the Synthesis of Aminobiphenylene
发明人：HEINRICH MARKUS; PRATSCH GERALD
权利人:HEINRICH MARKUS; PRATSCH GERALD; BASF SE
摘要:The present invention relates to a process for the synthesis of 2-aminobiphenylene and derivatives thereof by reacting a benzene diazonium salt with an aniline compound under basic reaction conditions.

专利号:US-2008280855-A1
优先权日:2005-06-22
标 题 :Process For the Production of Intermediates For the Preparation of Tricyclic Benzimidazoles
发明人：CHIESA MARIA VITTORIA; PALMER ANDREAS; BUHR WILM; ZIMMERMANN PETER JAN; BREHM CHRISTOF; SIMON WOLFGANG-ALEXANDER; POSTIUS STEFAN; KROMER WOLFGANG; ZANOTTI-GEROSA ANTONIO
权利人:NYCOMED GMBH
摘要:The invention relates to a process for the synthesis of compounds of the formula 1-a and compounds of the formula 1-b. n n n n n n n n n n The compounds of the formula 1-a and the compounds of the formula 1-b, in which the substituents R1, R2, R3, and Ar have the meanings indicated in the description, are valuable intermediates for the preparation of pharmaceutically active compounds.

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-5783577-A
优先权日:1995-09-15
标题 :Synthesis of quinazolinone libraries and derivatives thereof
发明人：HOUGHTEN RICHARD A; OSTRESH JOHN M
权利人:TREGA BIOSCIENCES INC
摘要:The present invention provides synthetic combinatorial libraries of organic compounds based on the quinazolinone ring.

专利号:US-6664282-B2
优先权日:1999-09-17
标 题:Synthesis of [3,5,7]-1H-imidazo [1,5-a]imidazol-2 (3H)- one compounds
发明人：ELABDELLAOUI HASSAN M; OSTRESH JOHN M; HOUGHTEN RICHARD A
权利人:TORREY PINES INST
摘要:Individual substituted [3,5,7]-1H-imidazo[1,5-a]imidazol-2(3H)-one compounds and their pharmaceutically-acceptable salts are disclosed, as are libraries of such compounds. Methods of preparing and using the libraries of compounds as well as individual compounds of the libraries are also disclosed.

专利号:US-8329880-B2
优先权日:2008-04-25
标 题 :Process for the preparation of naphthalen-2-yl-pyrazol-3-one intermediates useful in the synthesis of sigma receptor inhibitors
发明人：JOVER ANTONI TORRENS; ARJONA JORDI CORBERA; CUBERES-ALTISENT MARIA ROSA
权利人:JOVER ANTONI TORRENS; ARJONA JORDI CORBERA; CUBERES-ALTISENT MARIA ROSA; ESTEVE LABOR DR
摘要:The invention relates to a process for preparing naphthalen-2-yl-pyrazol-3-one intermediates, tautomers, and salts thereof, to novel intermediates, and to the use of the intermediates in the preparation of sigma receptor inhibitors.