2,4-二氯氟苯 反应生成 2,4-二氯-5-氟苯乙酮 参考文献:5-Hydroxymethyl-Oxazolidin-2-One-Derivatives And Their Uses As Antibacterials 标题:5-Hydroxymethyl-Oxazolidin-2-One-Derivatives And Their Uses As Antibacterials 摘要:本发明涉及一种新的嵌合抗生素,其化学式为i式,其中r1代表oh,Opo3H2或ocor5;r2代表h,Oh或opo3H2;a代表n或cr6;r3代表h或氟;r4是h,(C1-C3)烷基或环烷基;r5是天然氨基酸残基,天然氨基酸对映体或二甲氨基甘氨酸残基;r6代表h,烷氧基或卤素;n为0或1;以及i式化合物的盐(特别是药学上可接受的盐).这些嵌合化合物在制造治疗感染(例如细菌感染)的药物方面是有用的.
专利号:WO-2010058421-A3 优先权日:2008-11-18 标题 :A process for synthesis of 2, 4-dichloro-5- fluoroacetophenone (dcfa) 发明人:MANDAL SISIR; PATIL NARENDRA; SULEMAN INAMDUR; MORE VINOD; PURI PRASHANT 权利人:ADITYA BIRLA SCI & TECH CO LTD; MANDAL SISIR; PATIL NARENDRA; SULEMAN INAMDUR; MORE VINOD; PURI PRASHANT 摘要:A process for synthesis of 2,4-dichloro-5-fluoro acetophenone (DCFA) is disclosed. The process comprises first reacting 3,4-dichloronitrobenzene with potassium fluoride having bulk density in the range of 0.2 to 1.3, to form a fluorinated intermediate product, then reacting the intermediate product with chlorine to form dichlorofluorobenzene and finally acylating dichlorofluorobenzene using an acylating agent to form a mixture containing DCFA along with impurities, followed by purification and enrichment of DCFA in the mixture by melt crystallization.
专利号:WO-2010058421-A2 优先权日:2008-11-18 标题:A process for synthesis of 2, 4-dichloro-5- fluoroacetophenone (dcfa)
专利号:CN-116693375-B 优先权日:2023-08-08 标 题 :A kind of synthesis method of 2,4-dichloro-5-fluoroacetophenone
专利号:CN-116836114-A 优先权日:2023-08-31 标题 :Synthesis method of cyclopropanecarboxylic acid
专利号:CN-103304422-A 优先权日:2013-07-15 标 题 :A kind of one-pot synthesis method of 2,4-dichloro-3-nitro-5-fluorobenzoic acid
参考标题:Synthesis Of Some New 2,4-Disubstituted Thiazoles As Possible Antibacterial And Anti-Inflammatory Agents 作者:B.Shivarama Holla,K.V. Malini,B.Sooryanarayana Rao,B.K. Sarojini,N.Suchetha Kumari |发布日期:2003.3 摘要:A Series Of Arylthioureas (1), Aromatic Aldehyde Thiosemicarbazones (2) And 5-Aryl-2-Furfuraldehyde Thiosemicarbazones (3) Were Condensed With 2,4-Dichloro-5-Fluorophenacyl Bromide To Yield Respective Arylaminothiazoles, Arylidene/5-Aryl-2-Furfurylidene Hydrazinothiazoles (4). The Newly Synthesized Compounds Were Characterized By Ir, 1H-Nmr And Mass Spectral Studies. These Compounds Were Also Screened