合成目标产物 Ethyl 2,4-Dioxovalerate 主要起始原料 Diethyl Oxalate And Acetone
(文献来源)合成步骤主要原料 Diethyl Oxalate 和 Acetone
草酸二乙酯置于ammonium Chloride体系中,用 乙醇,丙酮 作为反应溶剂,化学反应生成 乙酰丙酮酸乙酯 参考文献:Synthesis Of Camptothecin And Analogs Thereof 标题:Synthesis Of Camptothecin And Analogs Thereof 摘要:使用一种新型含羟基的三环中间体合成紫杉醇和紫杉醇类似物的方法,以及由该过程产生的紫杉醇类似物.这些紫杉醇类似物是有效的拓扑异构酶i抑制剂,并显示出抗白血病和抗肿瘤活性.
专利号:US-6096898-A 优先权日:1999-10-22 标 题:One pot synthesis of 1,2,4-triazoles 发明人:PODHOREZ DAVID E; HULL JR JOHN W; BRADY CHRISTINE H 权利人:DOW AGROSCIENCES LLC 摘要:One pot synthesis of 1,2,4-triazoles uses thioimidate intermediate and 1,2-dichloroethane solvent.
专利号:WO-2025128848-A1 优先权日:2023-12-12 标题:Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use 发明人:HOUZE JONATHAN B; PANDYA BHAUMIK 权利人:VIGIL NEUROSCIENCE INC 摘要:The present disclosure provides compounds of Formula (I), useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 ('TREM2'). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).
专利号:WO-2025128873-A1 优先权日:2023-12-12 标题:Heterocyclic pyridinone compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use 发明人:HOUZE JONATHAN B; PANDYA BHAUMIK 权利人:VIGIL NEUROSCIENCE INC 摘要:The present disclosure provides compounds of Formula (I), useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 ('TREM2'). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).
专利号:US-4894456-A 优先权日:1987-03-31 标题 :Synthesis of camptothecin and analogs thereof 发明人:WALL MONROE E; WANI MANSUKH C; NICHOLAS ALLAN W; MANIKUMAR GOVINDARAJAN 权利人:RES TRIANGLE INST 摘要:A method for synthesizing camptothecin and camptothecin analogs using a novel hydroxyl-containing tricyclic intermediate and the camptothecin analogs produced by the process. The camptothecin analogs are effective inhibitors of topoisomerase I and show anti-leukemic and anti-tumor activity.
专利号:US-4981968-A 优先权日:1987-03-31 标题:Synthesis of camptothecin and analogs thereof 发明人:WALL MONROE E; WANI MANSUKH C; NICHOLAS ALLAN W; MANIKUMAR GOVINDARAJAN 权利人:RES TRIANGLE INST 摘要:A method for synthesizing camptothecin and camptothecin analogs using a novel hydroxyl-containing tricyclic intermediate and the camptothecin analogs produced by the process. The camptothecin analogs are effective inhibitors of topoisomerase I and show anti-leukemic and anti-tumor activity.
专利号:EP-0436653-A4 优先权日:1988-09-28 标题 :Synthesis of camptothecin and analogs thereof
[参考文献]: John M Fevig, Et Al. Preparation Of 1-(4-Methoxyphenyl)-1H-Pyrazolo[参考文献]: Stephen C Mckeown, Et Al. Identification Of Novel Pyrazole Acid Antagonists For The Ep1 Receptor. Bioorg Med Chem Lett. 2006 Sep 15;16(18):4767-71.
合成参考文献
摘要:Aitken, R. A.; Meehan, A., Science of Synthesis Knowledge Updates, (2014) 3, 162.