专利号:WO-0168615-A1 优先权日:2000-03-13 标题 :Quinazoline synthesis 发明人:DENER JEFFREY MARK; LEASE TIMOTHY G; NOVACK AARON ROBERT 权利人:CHEMRX ADVANCED TECHNOLOGIES I; DENER JEFFREY MARK; LEASE TIMOTHY G; NOVACK AARON ROBERT 摘要:The present invention relates to a method for making a compound of Formulas I, II and III. The method of the present invention also enables parallel and simultaneous synthesis of a plurality of compounds represented by Formulas I, II and III.
专利号:US-8895747-B2 优先权日:2009-07-27 标 题 :Method and substances for preparation of N-substituted pyridinium compounds 发明人:HEINDL DIETER; MAERZ HERIBERT; SCHMIDT AXEL 权利人:HEINDL DIETER; MAERZ HERIBERT; SCHMIDT AXEL; ROCHE DIAGNOSTICS OPERATIONS 摘要:Methods for the synthesis of N-substituted pyridinium compounds by using an N-heteroaryl substituted pyridinium salt (Zincke salt) and reacting it with a nucleophilic amine are provided. Novel purine-substituted pyridyl compounds, which may be useful reagents in the above reaction, are also disclosed.
专利号:US-2008039473-A1 优先权日:2006-08-08 标题:Preparation and utility of substituted quinazoline compounds with alpha-adrenergic blocking effects 发明人:GANT THOMAS G; SARSHAR SEPEHR 权利人:AUSPEX PHARMACEUTICALS INC 摘要:The present disclosure is directed to modulators of alpha-adrenergic receptors and pharmaceutically acceptable salts and prodrugs thereof, the chemical synthesis thereof, and the use of such compounds for the treatment and/or management of hypertension, cardiac failure, prostatitis, and benign prostatic hyperplasia, and any other condition in which it is beneficial to modulate an alpha-adrenergic receptor.
专利号:EP-1370552-B1 优先权日:2001-03-23 标题:Rho-kinase inhibitors 发明人:NAGARATHNAM DHANAPALAN; WANG CHUNGUANG 权利人:BAYER PHARMACEUTICALS CORP 摘要:Disclosed are compounds and derivatives thereof, their synthesis, and their use as Rho-kinase inhibitors. These compounds of the present invention are useful for inhibiting tumor growth, treating erectile dysfunction, and treating other indications mediated by Rho-kinase, e.g., coronary heart disease.
参考标题:An Expeditious, Practical Large Scale Synthesis Of 4-Amino-2-Chloro-6,7-Dimethoxyquinazolinazoline 作者:G. Kumaraswamy,Nivedita Jena,M. N. V. Sastry,B. Ashok Kumar |发布日期:2004.8 摘要:Converted To 8 By Treatment With Anhydrous Ammonia At Ambient Temperature In Dilute Thf. In Connection With Our Process Development Of (F)-Doxazocin Mesylate," We Had An Opportunity To Evaluate The Synthesis Of 8. Three Major Challenges Were Encountered In Course Of Reproducing The Above Synthetic Route: (I) Oxidation Of Vanillin (1) To Vaniliic Acid (2) Using Traditional Methods Such As Koh Melt5 Or
合成参考文献
摘要:Ghosh, B.; Maleczka, R. E., Jr., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 355.