3-氯氟苯置于硫酸,Potassium Nitrate体系中,化学反应生成 4-氯-2-氟硝基苯 参考文献:Synthesis,Structure-activity Relationships,And In Vivo Efficacy Of The Novel Potent And Selective Anaplastic Lymphoma Kinase (Alk) Inhibitor 5-Chloro-N2-(2-Isopropoxy-5-Methyl-4-(Piperidin-4-yl)Phenyl)-N4-(2-(Isopropylsulfonyl)Phenyl)Pyrimidine-2,4-Diamine (Ldk378) Currently In Phase 1 And Phase 2 Clinical Trials 标题:Synthesis,Structure-activity Relationships,And In Vivo Efficacy Of The Novel Potent And Selective Anaplastic Lymphoma Kinase (Alk) Inhibitor 5-Chloro-N2-(2-Isopropoxy-5-Methyl-4-(Piperidin-4-yl)Phenyl)-N4-(2-(Isopropylsulfonyl)Phenyl)Pyrimidine-2,4-Diamine (Ldk378) Currently In Phase 1 And Phase 2 Clinical Trials 摘要:The Synthesis,Preclinical Profile,And In Vivo Efficacy In Rat Xenograft Models Of The Novel And Selective Anaplastic Lymphoma Kinase Inhibitor 15B (Ldk378) Are Described. In This Initial Report,Preliminary Structure-Activity Relationships (Sars) Are Described As Well As The Rational Design Strategy Employed To Overcome The Development Deficiencies Of The First Generation Alk Inhibitor 4 (Tae684). Compound 15B Is Currently In Phase 1 And Phase 2 Clinical Trials With Substantial Antitumor Activity Being Observed In Alk-Positive Cancer Patients. DOI:10.1021/jm400402Q
专利号:US-5354439-A 优先权日:1990-07-16 标 题 :Process for the synthesis of fluorinated derivatives 发明人:FORAT GERARD; GILBERT LAURENT; LANGLOIS BERNARD 权利人:RHONE POULENC CHIMIE 摘要:A process for the synthesis of fluorinated organic compounds and a reagent suitable for use in the process. The process is carried out by exchange with fluorides, while preferably agitating the reaction medium with ultrasonic sound.
专利号:US-7217842-B2 优先权日:2001-04-12 标题:Catalysts for nucleophilic substitution, synthesis thereof, composition containing them and use thereof 发明人:SCHANEN VINCENT; CRISTAU HENRI-JEAN; TAILLEFER MARC 权利人:RHONE POULENC CHIMIE 摘要:The invention concerns novel catalysts for aromatic nucleophilic substitution. Said catalysts are compounds of the general formula (I), wherein: R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , identical or different, are selected among hydrocarbon radicals; the Pn's, advantageously the same, are selected among metalloid elements of column V of a period higher than nitrogen; Z is a metalloid element of column V, advantageously distinct from Pn; preferably a nitrogen (N, P, As, Sb). The invention is applicable to organic synthesis
专利号:FR-2664589-A1 优先权日:1990-07-16 标题 :PROCESS AND REAGENT FOR THE SYNTHESIS OF ARYLIC FLUORINE DERIVATIVES.
专利号:JP-H04244049-A 优先权日:1990-07-16 标 题 :Method for the synthesis of fluorinated derivatives
专利号:RU-2193554-C2 优先权日:1996-12-24 标题 :DERIVATIVES OF AROMATIC AMINES ELICITING EFFECT INHIBITING OAC, METHOD OF THEIR SYNTHESIS AND INHIBITOR OF нOAC
专利号:CN-120247709-A 优先权日:2025-05-27 标题 :Synthesis method of 2, 4-difluoronitrobenzene and 2-fluoro-5-chloronitrobenzene
参考文献:10.1055/s-0039-1691524 摘要:Roux A, Cisnetti F. Click Variations on the Synthesis of 2-Nitrophenyl-4-aryl-1,2,3-triazoles without Isolation of 2-Nitrophenyl Azides. Synlett. 2019 Dec 02;31(06):610–4. doi: 10.1055/s-0039-1691524. 参考文献:10.1055/s-2006-955596 摘要:Thomas A, Krafft E, Pinard E. Synthesis of Lu AA20465. Synfacts. 2006 Dec;2006(12):1205. doi: 10.1055/s-2006-955596.