专利号:WO-9948868-A9 优先权日:1998-03-26 标 题 :Heterocyclic classes of compounds for the modulating tyrosine protein kinase 发明人:FONG ANNIE; HANNAH ALISON; HARRIS G DAVIS; HIRTH PETER; HUBBARD STEVEN R; LANGECKER PETER; LIANG CONGXIN; MCMAHON GERALD; MOHAMMADI MOOSA; SCHLESSINGER JOSEPH; SHAWVER LAURA K; SUN LI; TANG PENG C; ULLRICH AXEL 权利人:SUGEN INC; UNIV NEW YORK; MAX PLANCK INST FUR BIOCHEMIE; FONG ANNIE; HANNAH ALISON; HARRIS G DAVIS; HIRTH PETER; HUBBARD STEVEN R; LANGECKER PETER; LIANG CONGXIN; MCMAHON GERALD; MOHAMMADI MOOSA; SCHLESSINGER JOSEPH; SHAWVER LAURA K; SUN LI; TANG PENG C; ULLRICH AXEL 摘要:The invention relates to certain indolinone-based and pyrazolylamide-based compounds, their method of synthesis, and combinatorial libraries consisting of the compounds. The invention also relates to methods of modulating the function of protein kinases using these compounds and methods of treating diseases by modulating the function of protein kinases and related signal transduction pathways.
专利号:US-6514981-B1 优先权日:1998-04-02 标题:Methods of modulating tyrosine protein kinase function with indolinone compounds 发明人:TANG PENG CHO; SUN LI 权利人:SUGEN INC 摘要:The invention relates to certain indolinone compounds, their method of synthesis, and a combinatorial library consisting of the indolinone compounds. The invention also relates to methods of modulating the function of protein tyrosine kinases using indolinone compounds and methods of treating diseases by modulating the function of protein tyrosine kinases and related signal transduction pathways.
专利号:CN-108997177-A 优先权日:2018-09-04 标题 :A kind of microwave-promoted method for the synthesis of N-benzenesulfonylnitroaniline compounds
专利号:US-2011046395-A1 优先权日:2008-01-25 标 题 :Process for the manufacture of a 6-fluoro-1,2-dihydro-2-oxo-3h-indol-3-ylidene derivative 发明人:RALL WERNER; PFRENGLE WALDEMAR; SCHNAUBELT JUERGEN 权利人:BOEHRINGER INGELHEIM INT 摘要:The present invention relates to a process for the manufacture of the compound 4-[(Z)-[[4-[(dimethylamino)methyl]phenyl]amino](6-fluoro-1,2-dihydro-2-oxo-3H-in-dol-3-ylidene)methyl]-benzenepropanoic acid and to a new intermediate for the synthesis.
专利号:CN-101811973-A 优先权日:2010-04-23 标 题 :A method for the synthesis of halogenated arylamines by highly selective liquid-phase hydrogenation under solvent-free conditions
专利号:US-6096763-A 优先权日:1995-02-23 标题 :α1a adrenergic receptor antagonists 发明人:HOFFMAN JACOB M; CHANG RAYMOND S L 权利人:MERCK & CO INC 摘要:This invention relates to novel compounds, their synthesis and use as selective α 1a adrenergic receptor antagonists. One application of the compounds is in the treatment of benign prostatic hyperplasia. The compounds are selective in their ability to relax smooth muscle tissue enriched in the α 1a receptor subtype without at the same time inducing hypotension. One such tissue is found surrounding the urethral lining. Therefore, one utility of the instant compounds is to provide acute relief to males suffering from benign prostatic hyperplasia, by permitting less hindered urine flow. Another utility of the instant compounds is provided by combination with a human 5-alpha reductase inhibitory compound, such that both acute and chronic relief from the effects of benign prostatic hyperplasia are achieved.
[参考文献]: I M Rietjens, Et Al. Different Metabolic Pathways Of 2,5-Difluoronitrobenzene And 2,5-Difluoroaminobenzene Compared To Molecular Orbital Substrate Characteristics. Chem Biol Interact. 1995 Jan;94(1):49-72. [参考文献]: Manuel A V Ribeiro Da Silva, Et Al. A Combined Experimental And Computational Thermodynamic Study Of Difluoronitrobenzene Isomers. J Phys Chem B. 2010 Oct 14;114(40):12914-25.
合成参考文献
摘要:Tomé, A. C., Science of Synthesis Knowledge Updates, (2015) 2, 119.