合成目标产物 Methyl Bromopyruvate 主要起始原料 Methanol And 3-Bromopyruvic Acid
(文献来源)合成步骤主要原料 Methanol 和 3-Bromopyruvic Acid
丙酮酸甲酯置于溴,溶剂黄146体系中,化学反应生成 溴代丙酮酸甲酯 参考文献: Efficient And Scalable Systhesis Of 2-(1'H-Indole-3'-Carbonyl)-Thiazole-4-Carboxylic Acid Methyl Ester And Its Structural Analogs[fr] Procédés De Synthèse Efficaces Et Adaptables De L'Ester De Méthyle D'Acide 2-(1'H-Indole-3'-Carbonyl)-Thiazole-4-Carboxylique Et De Ses Analogues Structuraux 标题: Efficient And Scalable Systhesis Of 2-(1'H-Indole-3'-Carbonyl)-Thiazole-4-Carboxylic Acid Methyl Ester And Its Structural Analogs[fr] Procédés De Synthèse Efficaces Et Adaptables De L'Ester De Méthyle D'Acide 2-(1'H-Indole-3'-Carbonyl)-Thiazole-4-Carboxylique Et De Ses Analogues Structuraux 摘要:合成2-(1'H-吲哚-3'-甲酰基)-噻唑-4-羧酸甲酯(ite)及其结构类似物的方法.这些方法包括缩合反应或缩合和氧化反应,以形成ite或其结构类似物的噻唑啉或噻唑基团.
专利号:US-4316029-A 优先权日:1979-06-22 标 题:Synthesis of vincaminic acid derivatives 发明人:ROSSEY GUY 权利人:SYNTHELABO 摘要:Vincaminic acid derivatives of formula (A) ##STR1## useful in treating cerebral insufficiency, are prepared by reacting 1-ethyl-2,3,4,6,7,12-hexahydroindolo[2,3-a]quinolizine with the 2,4-DNP hydrazone of ethyl or methyl bromopyruvate followed by (i) reduction of the Câ•?N bond and (ii) simultaneous cyclization with removal of the ketone-protecting group in either order.
专利号:US-10081610-B2 优先权日:2014-09-12 标题 :Efficient and scalable synthesis of 2-(1′h-indole-3′-carbonyl)-thiazole-4-carboxylic acid methyl ester and its structural analogs 发明人:SONG JIASHENG; ZHANG SUOMING; LI GUODONG; YANG LUQUING 权利人:ARIAGEN INC 摘要:Methods of synthesizing 2-(1′H-indole-3′-carbonyl)-thiazole-4-carboxylic acid methyl ester (ITE) and structural analogs thereof. The methods include condensation reactions or condensation and oxidation reactions to form the thiazoline or thiazole moiety of ITE or its structural analogs.
专利号:US-11465997-B2 优先权日:2017-06-22 标 题 :Synthesis of disorazoles and analogs thereof as potent anticancer agents 发明人:NICOLAOU KYRIACOS C; BELLAVANCE GABRIEL; BUCHMAN MAREK; PULUKURI KIRAN KUMAR; RIGOL STEPHAN 权利人:UNIV RICE WILLIAM M 摘要:In one aspect, the present disclosure provides disorazole analogs of the formula: Formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, drug conjugates with cell targeting moieties of the compounds are also provided.
专利号:US-2017291881-A1 优先权日:2014-09-12 标 题:Efficient and scalable synthesis of 2-(1'h-indole-3'-carbonyl)-thiazole-4-carboxylic acid methyl ester and its structural analogs
专利号:EP-3641891-A1 优先权日:2017-06-22 标 题 :Synthesis of disorazoles and analogs thereof as potent anticancer agents
专利号:US-2021155616-A1 优先权日:2017-06-22 标 题 :Synthesis of disorazoles and analogs thereof as potent anticancer agents
[参考文献]: Anne Katrine Kehler, Et Al. Variable Involvement Of The Perivascular Retinal Tissue In Carbonic Anhydrase Inhibitor Induced Relaxation Of Porcine Retinal Arterioles In Vitro. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4688-93. [参考文献]: Pinhong Chen, Et Al. Protecting-Group-Free Total Synthesis Of (+/-)-Subincanadine F. J Org Chem. 2009 Oct 2;74(19):7533-5.
合成参考文献
摘要:Westbrook, J. A.; Schaus, S. E., Science of Synthesis, (2007) 20, 1117. 摘要:Tang, Y.; Sun, X.-L., Science of Synthesis, (2008) 39, 505.