2242-77-5 = 86-96-4 反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Methanol,Water; Ph 10,Reflux 标题:Discovery Of Novel Quinazolines As Potential Anti-Tubulin Agents Occupying Three Zones Of Colchicine Domain 作者:Li,Wenlong; Et Al 参考文献:Bioorganic Chemistry 日期:2019 卷标:83 页码:380-390]
88-68-6 = 86-96-4 反应条件:1.1 Reagents: Potassium Carbonate,Sulfur Solvents: Dimethylformamide1.2 Reagents: Oxygen1.3 Reagents: Hydrochloric Acid Solvents: Water 标题:Convenient Synthesis Of Heterocycles By Sulfur-Assisted Carbonylation At Ordinary Pressure And Temperature 作者:Mizuno,Takumi; Et Al 参考文献:Heteroatom Chemistry 日期:1994 卷标:5 页码:437-40]
57-13-6 = 86-96-4 反应条件:1.1 Solvents: Dimethylacetamide; 3 Min; Rt 标题:A Green,Facile,And One-Pot Synthesis Of 2,4-(1H,3H)-Quinazolinediones Under Microwave Irradiations 作者:Nikpour,Farzad; Et Al 参考文献:Chemistry Letters 日期:2005 卷标:34(10) 页码:1438-1439]
57-13-6 = 86-96-4 反应条件:1.1 3 H,180 °C; 180 °C -> 120 °C1.2 Reagents: Sodium Hydroxide Solvents: Water1.3 Reagents: Hydrochloric Acid Solvents: Water; Acidified 标题:Synthesis,Characterisation And Biological Evaluation Of Quinazoline Derivatives As Novel Anti-Microbial Agents 作者:Prabhakar,V.; Et Al 参考文献:Organic Chemistry: Current Research 日期:2016 卷标:5(4) 页码:174/1-174/14]
= 86-96-4 反应条件:1.1 Solvents: Water 标题:4H-3,1-Benzoxazin-4-Ones. Ii. Reaction Of 1,2-Dihydro-2-Imino-4H-3,1-Benzoxazin-4-Ones With Nucleophilic Reagents And Their Conversion To 1,2,3,4-Tetrahydroquinazoline-2,4-Diones; Mechanism Of Condensation Reactions Of The Carboxyl Group Triggered By Carbodiimides 作者:Doleschall,Gabor; Et Al 参考文献:Monatshefte Fuer Chemie 日期:1964 卷标:95(4-5) 页码:1068-82]
590-28-3 = 86-96-4 反应条件:1.1 Reagents: Acetic Acid Solvents: Polyethylene Glycol; Rt -> 60 °C; 10 Min,50 - 60 °C 标题:A Facile And Convenient Approach For The One-Pot Synthesis Of 2,4(1H,3H)-Quinazolinediones 作者:Sharafi-Kolkeshvandi,Mahnaz; Et Al 参考文献:Chinese Chemical Letters 日期:2012 卷标:23(4) 页码:431-433]
590-28-3 = 86-96-4 反应条件:1.1 Reagents: Acetic Acid Solvents: Water; Overnight,Rt1.2 Reagents: Sodium Hydroxide; 4 H,Rt1.3 Reagents: Hydrochloric Acid Solvents: Water; < Ph 1,Rt 标题:Eco-Efficient One-Pot Synthesis Of Quinazoline-2,4(1H,3H)-Diones At Room Temperature In Water 作者:Tian,Xin-Chuan; Et Al 参考文献:Chemical & Pharmaceutical Bulletin 日期:2014 卷标:62(8) 页码:824-829]
610-15-1 = 86-96-4 反应条件:1.1 Reagents: Triethylamine Catalysts: Selenium Solvents: Tetrahydrofuran; 11 H,2 Mpa,170 °C 标题:Metal And Phosgene-Free Synthesis Of 1H-Quinazoline-2,4-Diones By Selenium-Catalyzed Carbonylation Of O-Nitrobenzamides 作者:Wu,Xiaowei; Et Al 参考文献:Tetrahedron Letters 日期:2010 卷标:51(11) 页码:1500-1503]
118-48-9 = 86-96-4 反应条件:1.1 Reagents: Urea Solvents: Dimethylformamide 标题:Syntheses Of Heterocycles. Lxxxix. Reactions Of Isatoic Anhydride With Derivatives Of Urea And Thiourea 作者:Kappe,Thomas; Et Al 参考文献:Monatshefte Fuer Chemie 日期:1967 卷标:98(1) 页码:214-18]
1885-29-6 = 86-96-4 反应条件:1.1 Reagents: 1,8-Diazabicyclo[5.4.0]Undec-7-Ene Solvents: Ethylene Glycol; 24 H,1 Bar,60 °C 标题:Room-Temperature Conversion Of Co2 Into Quinazoline-2,4(1H,3H)-Dione Using Deep Eutectic Solvents At Atmospheric Pressure With High Efficiency 作者:Chen,Yu; Et Al 参考文献:Reaction Chemistry & Engineering 日期:2022 卷标:7(9) 页码:1968-1977]
1885-29-6 = 86-96-4 反应条件:1.1 Catalysts: Phosphonium,Tributylethyl-,Salt With 1-Methyl-2,4-Imidazolidinedione (1:1); 30 H,0.1 Mpa,353.15 K 标题:Efficient Synthesis Of Quinazoline-2,4(1H,3H)-Dione Via Simultaneous Activated Co2 And 2-Aminobenzonitrile By 1-Methylhydantoin Anion-Functionalized Ionic Liquid Through The Multiple-Site Cooperative Interactions 作者:Chen,Tingting; Et Al 参考文献:Acs Sustainable Chemistry & Engineering 日期:2022 卷标:10(32) 页码:10699-10711]
1885-29-6 = 86-96-4 反应条件:1.1 Reagents: Carbon Dioxide Solvents: Water; Rt -> 150 °C; 5 H,5 Mpa,150 °C 标题:Carbon Dioxide Mediated Novel Synthesis Of Quinazoline-2,4(1H,3H)-Dione In Water 作者:Rasal,Kalidas B.; Et Al 参考文献:Organic Process Research & Development 日期:2016 卷标:20(12) 页码:2067-2073]
2242-77-5 = 86-96-4 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Methanol,Water; 3 H,Ph 10,Reflux; Reflux -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 3,Rt 标题:Discovery Of Novel Potent And Selective Ligands For 5-Ht2A Receptor With Quinazoline Scaffold 作者:Deng,Xinxian; Et Al 参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2015 卷标:25(18) 页码:3970-3974]
88-68-6 = 86-96-4 反应条件:1.1 Reagents: Diglyme; 5 H,Reflux 标题:Synthesis And Characterization Of New Bistriazole Quinazolinediones And Their Urease Inhibition Activities 作者:Akyuz,Gulay; Et Al 参考文献:Letters In Organic Chemistry 日期:2023 卷标:20(3) 页码:258-264]
88-68-6 = 86-96-4 反应条件:1.1 Reagents: 1,8-Diazabicyclo[5.4.0]Undec-7-Ene,Sulfur Solvents: Tetrahydrofuran 标题:Facile Synthesis Of 2,4-Dioxo-1,2,3,4-Tetrahydroquinazolines By Sulfur-Assisted Carbonylation With Carbon Monoxide 作者:Miyata,Toshiyuki; Et Al 参考文献:Heteroatom Chemistry 日期:1991 卷标:2(4) 页码:473-5]
88-68-6 = 86-96-4 反应条件:1.1 Reagents: Oxygen Catalysts: Cobalt Salen Solvents: Methanol 标题:Salcomine 作者:Parker,Kathlyn A.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001 卷标:1 页码:1-3]
= 86-96-4 反应条件:1.1 Reagents: Diisopropylcarbodiimide Solvents: Dimethylformamide; 20 Min,130 °C2.1 Reagents: Sulfuric Acid Solvents: Acetic Acid; 15 Min,110 °C3.1 Reagents: Potassium Hydroxide Solvents: Water; 15 Min,Reflux3.2 Reagents: Acetic Acid; Acidified 标题:Oxidative Ring Expansion Of Spirocyclic Oxindole Derivatives 作者:Bergman,Jan; Et Al 参考文献:Journal Of Organic Chemistry 日期:2014 卷标:79(19) 页码:9065-9073]
530-62-1 + 118-48-9 = 86-96-4 反应条件:1.1 Reagents: Ammonia Solvents: Dichloromethane; 30 Min,Reflux1.2 2 H,Reflux 标题:One-Pot Syntheses Of Some New 2,4(1H,3H)-Quinazolinedione Derivatives In The Absence Of Catalyst 作者:Mohammadi,Ali Asghar 参考文献:Journal Of Heterocyclic Chemistry 日期:2017 卷标:54(3) 页码:2075-2078]
88-68-6 = 86-96-4 反应条件:1.1 Reagents: Triphenyl Phosphite,1,5-Diazabicyclo[4.3.0]Non-5-Ene Solvents: Acetonitrile; 1 H,Rt 标题:Synthesis Of N-Unsubstituted And N3-Substituted Quinazoline-2,4(1H,3H)-Diones From O-Aminobenzamides And Co2 At Atmospheric Pressure And Room Temperature 作者:Zhang,Lin; Et Al 参考文献:Organic Letters 日期:2023 卷标:25(14) 页码:2471-2475]
610-15-1 = 86-96-4 反应条件:1.1 Catalysts: Stannous Chloride,Dichlorobis(Triphenylphosphine)Palladium Solvents: Tetrahydrofuran 标题:Palladium Complex-Catalyzed Intermolecular Reductive N-Heterocyclization: Novel Synthesis Of Quinazoline Derivatives From 2-Nitrobenzaldehyde Or 2-Nitrophenyl Ketones With Formamide 作者:Akazome,Motohiro; Et Al 参考文献:Journal Of Organometallic Chemistry 日期:1995 卷标:494(1-2) 页码:229-33]
88-96-0 = 86-96-4 反应条件:1.1 Reagents: Iodobenzene Diacetate Solvents: Methanol; Rt 标题:Onsh: Optimization Of Oxidative Alkylamination Reactions Through Study Of The Reaction Mechanism 作者:Verbeeck,Stefan; Et Al 参考文献:Journal Of Organic Chemistry 日期:2010 卷标:75(15) 页码:5126-5133]
88-96-0 = 86-96-4 反应条件:1.1 Reagents: Iodobenzene Diacetate Solvents: Methanol 标题:Oxidative Cyclization Of Diamides By Phenyliodoso Acetate 作者:Beckwith,Athelstan L. J.; Et Al 参考文献:Australian Journal Of Chemistry 日期:1990 卷标:43(3) 页码:451-61]
24424-99-5 + 88-68-6 = 86-96-4 反应条件:1.1 Catalysts: 4-(Dimethylamino)Pyridine Solvents: Acetonitrile; 12 H,Rt 标题:Dmap-Catalyzed One-Pot Synthesis Of Quinazoline-2,4-Diones From 2-Aminobenzamides And Di-Tert-Butyl Dicarbonate 作者:Chen,Hui; Et Al 参考文献:Acs Omega 日期:2020 卷标:5(16) 页码:9614-9623]
118-48-9 = 86-96-4 反应条件:1.1 Reagents: Urea; Rt 标题:Synthesis And Analgesic Activity Of 6-Amino-2-Piperazinylquinazolines 作者:Kornylov,A. Yu.; Et Al 参考文献:Visnik Odes'Koho Natsional'Noho Universitetu 日期:2021 卷标:26(1) 页码:74-84]
118-48-9 = 86-96-4 [标题:Reaction Conditions 标题:Product Class 13: Quinazolines 作者:Kikelj,D. 参考文献:Science Of Synthesis 日期:2004 卷标:16 页码:573-749]
917-61-3 = 86-96-4 反应条件:1.1 Solvents: Acetic Acid,Water; 35 °C; 30 Min,35 °C1.2 Reagents: Sodium Hydroxide; Cooled; 12 H,Cooled1.3 Reagents: Sulfuric Acid Solvents: Water; Ph 7 标题:Synthesis,Spectroscopic Characterization And X-Ray Analysis Of 6-Nitroquinazoline-2,4(1H,3H)-Dione 作者:Kesternich,Viictor; Et Al 参考文献:Journal Of The Chilean Chemical Society 日期:2013 卷标:58(3) 页码:1817-1819]
31143-83-6 + 590-28-3 = 86-96-4 反应条件:1.1 Reagents: Acetic Acid Solvents: Polyethylene Glycol; 25 Min,50 - 60 °C 标题:Condensation Reaction Of Ethyl 4-Oxo-4H-Benzo[d][1,3]Oxazine-2-Carboxylates With Potassium Cyanate: 2,4(1H,3H)-Quinazolinediones Synthesis 作者:Nikpour,Farzad; Et Al 参考文献:Heterocycles 日期:2012 卷标:85(11) 页码:2745-2748]
88-68-6 = 86-96-4 反应条件:1.1 Catalysts: Iodine Solvents: 1-Butyl-3-Methylimidazolium Tetrafluoroborate; 45 Min,80 °C; 80 °C -> Rt 标题:Green Synthesis Of Quinazolinone Derivatives Catalyzed By Iodine In Ionic Liquid 作者:Wang,Shu-Liang; Et Al 参考文献:Synthetic Communications 日期:2012 卷标:42(3) 页码:341-349]
= 86-96-4 反应条件:1.1 Reagents: Sulfuric Acid,Potassium Peroxymonosulfate Sulfate (2Khso5.Khso4.K2So4) Solvents: Tetrahydrofuran; Rt -> 40 °C; Overnight,40 °C 标题:A Radical Approach For The Selective C-H Borylation Of Azines 作者:Kim,Ji Hye; Et Al 参考文献:Nature (London 日期:2021 卷标:595(7869) 页码:677-683
专利号:US-11542269-B2 优先权日:2018-01-03 标 题:Prins reaction and compounds useful in the synthesis of halichondrin macrolides and analogs thereof 发明人:CHOI HYEONG-WOOK; FANG FRANCIS G 权利人:EISAI R&D MAN CO LTD 摘要:The invention provides methods utilizing Prins reaction in the preparation of compounds that may be useful as intermediates in the synthesis of halichondrin macrolides and analogs thereof. The invention also provides compounds that may be useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.
专利号:US-10913749-B2 优先权日:2015-05-07 标 题 :Macrocyclization reactions and intermediates and other fragments useful in the synthesis of halichondrin macrolides 发明人:FANG FRANCIS G; KIM DAE-SHIK; CHOI HYEONG-WOOK; CHASE CHARLES E 权利人:EISAI R&D MAN CO LTD 摘要:The invention provides methods for the synthesis of a halichondrin macrolides through a macrocyclization strategy. The macrocyclization strategy of the present invention involves subjecting a non-macrocyclic intermediate to a carbon-carbon bond-forming reaction (e.g., an olefination reaction (e.g., Horner-Wadsworth-Emmons olefination), catalytic Ring-Closing Olefin Metathesis, or Nozaki-Hiyama-Kishi reaction) to afford a macrocyclic macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.
专利号:US-11136335-B2 优先权日:2016-06-30 标题:Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof 发明人:CHASE CHARLES E; CHOI HYEONG-WOOK; ENDO ATSUSHI; FANG FRANCIS G; KIM DAE-SHIK 权利人:EISAI R&D MAN CO LTD 摘要:The invention provides methods for the synthesis of a halichondrin macrolides or analogs thereof through a cyclization reaction strategy. The strategy of the present invention involves subjecting an intermediate to Prins reaction conditions to afford a macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides or analogs thereof and methods for preparing the same.
专利号:US-6376667-B1 优先权日:1997-11-26 标 题 :Solid phase synthesis of heterocycles 发明人:CASTELHANO ARLINDO L; SHAO HUI 权利人:OSI PHARM INC 摘要:Methods and compounds for the synthesis of heterocycles, including pyrimidine-2,4-diones, are disclosed. Also disclosed are solid supports useful for solid phase synthesis, and methods for making the solid supports.
专利号:US-5783698-A 优先权日:1996-01-23 标题:Chemical synthesis of 1,3-disubstituted quinazolinediones 发明人:SMITH ADRIAN LEONARD 权利人:MERCK SHARP & DOHME 摘要:The present invention relates to a method for the synthesis of 1,3-disubstituted quinazolinedione derivatives which comprises: n (a) reacting a haloformate functionalized polystyrene resin with a substituted anthranilic acid derivative under conditions effective to form a urethane-linkage; n (b) reacting the product of step (a) with a primary amine under conditions effective to form an anthranilamide derivative; n (c) heating the anthranilamide to effect intramolecular cyclization thereby liberating the 1,3-disubstituted quinazolinedione derivative from the resin into solution; and n (d) isolating the 1,3-disubstituted quinazolinedione by filtration and solvent removal.
专利号:US-9315483-B2 优先权日:2007-09-13 标题 :Synthesis of deuterated catechols and benzo[D][1,3]dioxoles and derivatives thereof 发明人:JONES ANDREW D; ZELLE ROBERT E; SILVERMAN I ROBERT 权利人:CONCERT PHARMACEUTICALS INC 摘要:The present invention provides a convenient and efficient process for the synthesis of d 2 -benzo[d][1,3]dioxoles.
摘要:Kang, F.-A.; Yang, S.-M., Science of Synthesis Knowledge Updates, (2015) 2, 209. 摘要:Sellars, J. D., Science of Synthesis Knowledge Updates, (2014) 1, 400. 摘要:Chimica Therapeutica., 3(100), 1968 摘要:A. Albert and J. N. Phillips. J. Chem. Soc. 1956, 1294. 摘要:J. Gut, M. Prystas, J. Jonas and F. Sorm, Collect. Czech. Chem. Commun. 26, 974 (1961).