专利号:US-4013658-A 优先权日:1975-07-03 标 题 :Synthesis of 3,5-diphenyl-4(1h)-pyridazinones 发明人:ABDULLA RIAZ F 权利人:LILLY CO ELI 摘要:A series of 3,5-diphenyl-4(1H)-pyridazinones are synthesized by a two-step process, both steps of which are new. In the first step, a phenylglyoxyloyl halide is reacted with a styrylamine in the presence of a base to form a 1-amino-2,4-diphenyl-1-buten-3,4-dione. In the second step, the enaminoketone formed in the first step is reacted with hydrazine or an alkylhydrazine to form the pyridazinone. Both steps of the reaction proceed in good yields at temperatures in the range of from about 0° C. to about 40° C. in the common reaction solvents.
专利号:US-8957254-B2 优先权日:2009-07-06 标题 :Process for chemical synthesis from an alkenone made from a halogenated precursor 发明人:BRAUN MAX; PALSHERM STEFAN; CLAASSEN UTA; LAMBERT ALAIN 权利人:BRAUN MAX; PALSHERM STEFAN; CLAASSEN UTA; LAMBERT ALAIN; SOLVAY 摘要:Process for synthesizing a chemical, in particular an agriculturally or pharmaceutically active compound, including: a first step comprising reacting a carboxylic acid halide with a vinyl ether to prepare a halogenated precursor of an alkenone; a second step comprising eliminating hydrogen halide from such precursor to form an alkenone, preferably by thermolysis under specific conditions; and a third step which uses the formed alkenone as a building block to synthesize the chemical. First step may be done in a liquid reaction medium comprising an alkenone or a halogenated alkenone precursor, or in a liquid reaction medium in turbulent state, specifically by creation of gas bubbles of the carboxylic acid halide herein. Second step may include a flash thermolysis, vacuum thermolysis, thermolysis under stripping with inert gas, and/or a thermolysis at a temperature from >90° C. to 120° C. Third step preferably comprises reacting the alkenone with a nitrogen-containing compound.
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参考标题:Synthesis Of 3-(5H-Pyrazolyl)Cyclobutanone Derivatives 作者:Pengfei Fu,Zeqing Li,Yuqiang Wang,Pei Yu 摘要:A 3-(5H-Pyrazolyl)-Cyclobutanone Derivative Was Synthesized Via Two Different Optimized Routes. In The First Route, The Substitutional Pyrazole Olefins Was Prepared As A Precursor, The Target Molecule Was Synthesized Via [2 + 2]-Cycloaddition By Using Pyrazols Olefins And Ketene In Total Yield Of 3 %. In The Second Route, The Four-Member Ring Cyclobutanone Fragment Was Made First, Then The Pyrazole Ring Was Obtained Through Cyclization, Offering The Target Molecule With A Yield Of 8.6 %.
合成参考文献
参考文献:10.1007/s11030-025-11121-w 摘要:Abdel-Maksoud MS, Eitah HE, Hassan RM, Abd-Allah WH. Design and synthesis of novel pyrimidine-pyrazole hybrids with dual anticancer and anti-inflammatory effects targeting BRAFV600E and JNK. Mol Divers. 2025 Feb 22;29(6):6205–25. doi: 10.1007/s11030-025-11121-w.