2-amino-9H-thioxanthen-9-one3-(Dimethylamino)propyl chloride2-carboxyphenyl 4-chlorophenyl sulphideThiosalicylic acid2-chloro-9-(3-dimethylamino-propyl)-thioxanthen-9-olsulfure de pentamethylenethioxanthene2-Chloro-9-(4-tetrahydrothiopyranyl)thioxanthen-9-ol
合成工艺路线路线简述
合成目标产物 2-Chlorothioxanthone 主要起始原料 Nsc54679
6469-85-8 = 86-39-5 反应条件:1.1 Reagents: Sulfuric Acid; 1 H,100 °C 标题:Catalyst-Controlled Stereoselective Barton-Kellogg Olefination 作者:Schmidt,Tanno A.; Et Al 参考文献:Angewandte Chemie 日期:2021 卷标:60(44) 页码:23911-23916]
22096-70-4 = 86-39-5 反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Methanol; Rt; 1 H,80 °C; 80 °C -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water1.3 Reagents: Sulfuric Acid; Rt; 12 H,100 °C; 100 °C -> Rt1.4 Reagents: Sodium Bicarbonate Solvents: Water 标题:A Mild And Facile Synthesis Of Aryl And Alkenyl Sulfides Via Copper-Catalyzed Deborylthiolation Of Organoborons With Thiosulfonates 作者:Yoshida,Suguru; Et Al 参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(93) 页码:16613-16616]
113-59-7 = 86-39-5 反应条件:1.1 Reagents: Oxygen Catalysts: N-Hydroxysuccinimide,1,3,5-Triazine-2,4,6-Triamine Homopolymer Solvents: Acetonitrile; 16 - 40 H,Rt 标题:A Metal-Free Heterogeneous Photocatalyst For The Selective Oxidative Cleavage Of C=c Bonds In Aryl Olefins Via Harvesting Direct Solar Energy 作者:Zhang,Yu; Et Al 参考文献:Green Chemistry 日期:2020 卷标:22(14) 页码:4516-4522]
107572-07-6 = 86-39-5 反应条件:1.1 Reagents: Pyridine Catalysts: Cobalt,Bis[[2,3-Butanedione Di(Oximato-Kn)](1-)]Chloro(Pyridine)-,(Oc-6-42)- Solvents: Dichloromethane; 24 H,Rt 标题:Direct Excitation Of Aldehyde To Activate The C(Sp2)-H Bond By Cobaloxime Catalysis Toward Fluorenones Synthesis With Hydrogen Evolution 作者:Guo,Jia-Dong; Et Al 参考文献:Angewandte Chemie 日期:2023 卷标:62(7)]
73129-22-3 = 86-39-5 [标题:Reaction Conditions 标题:Neurotropic And Psychotropic Agents. Clxviii. Tricyclic Psychotropic Agents Containing Two Chalcogen Atoms In The Central Ring: 8-Substituted 6-(4-Piperidyl)-6H-Dibenz[b,E]-1,4-Oxathiepins 作者:Sindelar,Karel; Et Al 参考文献:Collection Of Czechoslovak Chemical Communications 日期:1982 卷标:47(11) 页码:3077-93]
446-52-6 = 86-39-5 反应条件:1.1 Reagents: Potassium Carbonate Solvents: Dimethylformamide; 150 °C2.1 Reagents: Pyridine Catalysts: Cobalt,Bis[[2,3-Butanedione Di(Oximato-Kn)](1-)]Chloro(Pyridine)-,(Oc-6-42)- Solvents: Dichloromethane; 24 H,Rt 标题:Direct Excitation Of Aldehyde To Activate The C(Sp2)-H Bond By Cobaloxime Catalysis Toward Fluorenones Synthesis With Hydrogen Evolution 作者:Guo,Jia-Dong; Et Al 参考文献:Angewandte Chemie 日期:2023 卷标:62(7)]
92-38-6 = 86-39-5 反应条件:1.1 Reagents: Oxygen Catalysts: Acetic Acid,2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone,Tert-Butyl Nitrite Solvents: 1,2-Dichloroethane; 12 H,Rt 标题:Visible-Light-Induced Aerobic Oxidation Of Benzylic C(Sp 3 )-H Of Alkylarenes Promoted By Ddq,Tert -Butyl Nitrite,And Acetic Acid 作者:Pan,Decheng; Et Al 参考文献:Synlett 日期:2019 卷标:30(2) 页码:218-224]
1449571-63-4 = 86-39-5 反应条件:1.1 Reagents: Disodium Sulfide Solvents: Dimethylformamide; 1 H,60 °C 标题:A Convenient Synthesis Of 9H-Thioxanthen-9-Ones And Their Aza-Analogs 作者:Kobayashi,Kazuhiro; Et Al 参考文献:Heterocycles 日期:2013 卷标:87(12) 页码:2577-2587]
6469-93-8 = 86-39-5 反应条件:1.1 Reagents: 3,5-Dinitrobenzotrifluoride,1,1,1,3,3,3-Hexafluoro-2-Propanol Solvents: Dichloromethane; 24 H,-30 °C1.2 Reagents: Formaldehyde Solvents: Acetonitrile,Water; -30 °C; 16 H,Rt1.3 Reagents: Dipotassium Phosphate; 20 H 标题:Photoexcited Nitroarenes For The Oxidative Cleavage Of Alkenes 作者:Ruffoni,Alessandro; Et Al 参考文献:Nature (London 日期:2022 卷标:610(7930) 页码:81-86]
41932-38-1 = 86-39-5 反应条件:1.1 Reagents: Hexadecyltrimethylammonium Bromide,Oxygen Catalysts: Bismuth Tungsten Oxide (Bi2Wo6) Solvents: Water; 24 H,Rt 标题:Rapid Microwave Synthesis Of Bi2Wo6 For C=c Bonds Oxidative Cleavage To Ketones With Visible Light Irradiation In Aerobic Micellar Medium 作者:Liu,Tianxiang; Et Al 参考文献:Journal Of Catalysis 日期:2023 卷标:417 页码:41-51]
1229-38-5 = 86-39-5 反应条件:1.1 Reagents: Permanganic Acid (Hmno4),Potassium Salt (1:1) 标题:Selective Oxidation Of Thioxanthene Derivatives 作者:Tammilehto,Seija; Et Al 参考文献:Acta Pharmaceutica Suecica 日期:1986 卷标:23(5) 页码:289-94]
119-80-2 = 86-39-5 反应条件:1.1 Catalysts: Sulfuric Acid Solvents: Water; Rt; 4 H,Cooled1.2 Reagents: Water 标题:Synthesis Of Thiaxanthone Derivatives 作者:Mao,Xue-Feng; Et Al 参考文献:Huaxue Shiji 日期:2008 卷标:30(12) 页码:932-934]
专利号:US-9969823-B1 优先权日:2011-09-01 标题 :Synthesis and polymerization of vinyl triazolium ionic liquids 发明人:LUEBKE DAVID; NULWALA HUNAID; MATYJASZEWSKI KRZYSZTOF; ADZIMA BRIAN 权利人:US ENERGY; THE US DEPARTMENT OF ENERGY 摘要:Herein, we describe polymerized ionic liquids, demonstrate the synthesis of polymerized ionic liquids, and demonstrate the polymerization of triazolium monomers. One embodiment shows the polymeriazation of the triazolium monomers with bis(trifluoromethanesulfonyl)imide anions. In another embodiment we show the feasibility of copolymerizing with commodity monomers such as styrene using free radical polymerization techniques.
专利号:EP-4428168-A1 优先权日:2023-03-08 标 题 :Polyurethane/oligomeric urethane synthesis method by radiation 发明人:AKBULUT HÜSEYIN; ÇEL KBA SENA; ENADA SEHER; U AKLI MÜGE; DEM RBAY DUYGU 权利人:CHT TURKEY KIMYA SANAYI VE TICARET A S 摘要:In particular, the invention relates to the synthesis of radiation-curable polyurethane/oligomeric urethane dispersions of anionic and cationic characters, containing neutralization techniques characterized by the selection of counter ions as monomers and/or agents which can be polymers acting as promoters under radiation, to a radiation polyurethane/oligomeric urethane synthesis method that enables the creation of radiation curable binder systems without using cosolvents, surfactants, emulsifiers, defoamers, stabilizers and additives, wherein all components of the radiation-curable binder systems can be polymerized.
专利号:US-6031014-A 优先权日:1998-12-08 标题:Initiator compositions and methods for their synthesis and use 发明人:CRIVELLO JAMES V 摘要:Cationic polymerization initiators of formula ##STR1## are disclosed. The acyl sulfonium salts of the present invention differ from known acyl sulfonium initiators in that the substituents R 2 and R 3 on the sulfur are larger and more complex than the lower alkyl and lower alkylene of known photoinitiators. Processes for the synthesis of the novel acyl sulfonium salts and prepolymer compositions containing them are also disclosed.
专利号:US-9175026-B2 优先权日:2011-03-23 标题:Synthesis of thioether containing trialkoxysilanes 发明人:GARRELL ROBIN L; TUCKER-SCHWARTZ ALEXANDER K 权利人:GARRELL ROBIN L; TUCKER-SCHWARTZ ALEXANDER K; UNIV CALIFORNIA 摘要:The invention relates to a radical-initiated thiol-ene or thiol-yne “clickâ€? reaction that provides a simple and efficient route to diverse trialkoxysilanes. Trialkoxysilanes made in this way are obtained in quantitative to near-quantitative yields with high purity without any or minimal purification. A wide range of functional groups is tolerated in this approach, and even complex alkenes click with the silane precursors. The modular nature of these radical-based thiol-ene or thiol-yne “clickâ€? reactions allows a wide variety of pendant groups to be coupled to silane compounds that can then be coupled to a wide variety surfaces in order to modify their material properties. Consequently, such radical initiated thiol-ene and thiol-yne reactions provide facile and efficient methods for preparing an enormous number of surface-active functional trialkoxysilanes.
专利号:US-8475998-B2 优先权日:2010-12-20 标 题 :Compound synthesis method, microarray, acid-transfer composition, and biochip composition 发明人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI 权利人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI; SAMSUNG ELECTRONICS CO LTD; JSR CORP 摘要:A compound synthesis method includes bonding a first compound to a substrate to form a first film. A second film is formed on the first film using an acid-transfer composition including (A) a polymer that includes a structural unit shown by a following formula (1) and a structural unit shown by a following formula (2), (B) a photoacid generator shown by a following formula (3), and (C) a sensitizer shown by a following formula (4). The second film is exposed to remove the protecting group from the first compound under an exposed area of the second film. An acid generated in the exposed area of the second film is transferred to the first film. The second film after being exposed is removed. A second compound is bonded to the first compound from which the protecting group has been removed.
专利号:US-2005170281-A1 优先权日:2002-06-21 标题:Method of cleaving labile functional groups from chemical compounds 发明人:STENGELE KLAUS-PETER 摘要:The present invention provides a method of cleaving labile functional groups from molecules by exposure to electromagnetic radiation in which the molecules are contacted with a chemical compound whose triplet state is energetically higher than the triplet state of the labile functional group and are then exposed to electromagnetic radiation, with the labile functional group and the suitable chemical compound having different absorption maxima for electromagnetic radiation. Further, the invention provides a method of manufacturing DNA chips by spatially addressed, light-controlled nucleotide synthesis on solid substrates. In addition, the present invention provides a chemical composition comprising a molecule with a labile functional group and a chemical compound whose triplet state is higher than the triplet state of the labile functional group, with the labile functional group and the chemical compound having different absorption maxima for electromagnetic radiation, and describes the use of the chemical composition in the manufacture of DNA chips.
[参考文献]: J E Pettersen, Et Al. Identification Of 2-Chlorothioxanthen-9-One In Gastric Aspirate In A Case Of Chlorprothixene Poisoning. J Pharm Sci. 1981 Jul;70(7):812-3.