CAS: 93-98-1; Benzanilide

该化合物是属于氨化物类的有机化合物,其特征是通过碳基(C=O)链接将苯环附于一个Aniline组,该化合物一般是白色的脱白晶状固体,以其在水中的溶性相对较低而闻名,但在乙醇和乙酮等有机溶剂中可溶解.Benzanilide有一个熔点,一般范围为130-135C,表明其在室温中的固态状态,经常用于有机合成和作为生产各种药品和染料的中间体.此外,该化合物还展示了某些生物活动,使其对药用化学具有兴趣.安全考虑,如同许多有机化合物一样,包括适当的处理和储存以避免接触.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

pyridine Benzophenone oxime benzenesulfonyl chloride benzoic acid methyl esterN,N-dibenzoylaniline N,N'-diphenylbenzamidine N-(4-chlorophenyl)benzamide N-(2-chlorophenyI)benzamide

合成工艺路线路线简述

  • 4686-14-0 = 93-98-1
    反应条件:1.1 Catalysts: Water Solvents: Dimethylformamide; 24 H,120 °C1.2 Reagents: Sodium Hydroxide Solvents: Water; 10 Min,Rt
    标题:Formation Of Amides From Imines Via Cyanide-Mediated Metal-Free Aerobic Oxidation
    作者:Seo,Hong-Ahn; Cho,Yeon-Ho; Lee,Ye-Sol; Cheon,Cheol-Hong
    参考文献:Journal Of Organic Chemistry 日期:2015 卷标:80(24) 页码:11993-11998]

    65-85-0 = 93-98-1
    反应条件:1.1 Reagents: Diisopropylethylamine,N-[1-(Cyano-2-Ethoxy-2-Oxoethylideneaminooxy)Dimethylamino(Morpholino)Uronium He... Solvents: Tetrahydrofuran,Water; 24 H,Ph 10.8,25 °C
    标题:Evaluation Of Safe Mixed Solvents In N-Phenylbenzamide Synthesis For Alteration Of Hazardous Dipolar Aprotic Solvents In Amide Drug Syntheses
    作者:Islam,Tariqul; Sarker,Zaidul Islam Md; Uddin,Abm Helal; Rashid,Shah Samiur; Bin,Liew Kai
    参考文献:Tetrahedron 日期:2023 卷标:131]

    98-88-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Solvents: Tetrahydrofuran; 0 °C; 0 °C -> Rt; 12 H,Rt
    标题:α-Imino Iridium Carbenes From Imidoyl Sulfoxonium Ylides: Application In The One-Step Synthesis Of Indoles
    作者:Caiuby,Clarice A. D.; De Jesus,Matheus P.; Burtoloso,Antonio C. B.
    参考文献:Journal Of Organic Chemistry 日期:2020 卷标:85(11) 页码:7433-7445]

    591-50-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Catalysts: (Sp-4-1)-(Acetonitrile)Dichloro[1-(4,6-Dimethoxy-1,3,5-Triazin-2-Yl)-1,3-Dihydro... Solvents: 1,4-Dioxane; 6 H,3 Atm,100 °C
    标题:N-Heterocyclic Carbine Palladium Complex Crystal And Its Synthesis Method And Application In Preparing Amide Compound
    参考文献:China]

    591-50-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Catalysts: (Sp-4-3)-[3′,4′-Bis(4,5-Dihydro-4,4-Dimethyl-2-Oxazolyl-Kn3)[1,1′-Biphenyl]-4-Ol... (Solid-Supported) Solvents: Acetonitrile; Rt -> 120 °C; 6 H,100 Psi,120 °C
    标题:Catalytic Process For Synthesizing Ester Compounds And Amide Compounds
    参考文献:United States]

    98-88-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Solvents: Dichloromethane; 0.5 H,0 °C; 0 °C -> Rt; 2 H,Rt
    标题:Substituted 2,4-Diaminopyrimidine Compounds As Protein Kinase Inhibitors And Their Preparation,Pharmaceutical Compositions And Use In The Treatment Of Diseases
    参考文献:China]

    7510-33-0 = 93-98-1
    反应条件:1.1 Reagents: Tetrabutylammonium Perchlorate,4-Methyl-N,N-Bis[2-[[(4-Methylphenyl)Sulfonyl]Oxy]Ethyl]Benzenesulfonamide Solvents: Dimethylformamide; 25 °C1.2 Reagents: Sodium Bicarbonate Solvents: Water; Basified,25 °C
    标题:Electrochemical Reduction Of α-Diketones And α-Diimines In The Presence Of A Bielectrophilic Substrate: Synthesis Of New Aza-Crown Compounds
    作者:Medini,Hayet Khemis; Mekni,Nejib Hussein; Aoun,Sami Ben; Boujlel,Khaled
    参考文献:Journal Of The Electrochemical Society 日期:2017 卷标:164(2)]

    591-50-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Catalysts: Palladium (Merrifield Resin-Supported Bisoxazoline Complexes),3′,4′-Bis(4,5-Dihydro-4,4-Dimethyl-2-Oxazolyl)[1,1′-Biphenyl]-4-Ol (Palladium Complexes,Merrifield Resin-Supported) Solvents: Acetonitrile; 100 Psi,Rt -> 120 °C; 6 H,120 °C
    标题:A Palladium-Bisoxazoline Supported Catalyst For Selective Synthesis Of Aryl Esters And Aryl Amides Via Carbonylative Coupling Reactions
    作者:Ibrahim,Mansur B.; Suleiman,Rami; Fettouhi,Mohammed; El Ali,Bassam
    参考文献:Rsc Advances 日期:2016 卷标:6(82) 页码:78826-78837]

    591-50-4 = 93-98-1
    反应条件:1.1 Reagents: 1,8-Diazabicyclo[5.4.0]Undec-7-Ene Catalysts: Palladium Solvents: Dimethylacetamide; 115 °C
    标题:1,8-Diazabicyclo[5.4.0]Undec-7-Ene
    作者:Savoca,Ann C.; Urgaonkar,Sameer
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2006 卷标:1 页码:1-11]

    574-66-3 = 93-98-1
    反应条件:1.1 Catalysts: Benzenesulfonic Acid,4-Ethenyl-,Sodium Salt (1:1),Polymer With Diethenylbenze... (Neutralized) Solvents: Benzonitrile; 1 H,130 °C
    标题:In Situ Functionalized Sulfonic Copolymer Toward Recyclable Heterogeneous Catalyst For Efficient Beckmann Rearrangement Of Cyclohexanone Oxime
    作者:Li,Difan; Mao,Dan; Li,Jing; Zhou,Yu; Wang,Jun
    参考文献:Applied Catalysis 日期:2016 卷标:510 页码:125-133]

    93-97-0 = 93-98-1
    反应条件:1.1 Catalysts: Titania Solvents: Ethanol; 2.5 H,25 - 35 °C
    标题:Photocatalytic Synthesis Of Anilides From Nitrobenzenes Under Visible Light Irradiation: 2 In 1 Reaction
    作者:Zand,Zahra; Kazemi,Foad; Partovi,Adel
    参考文献:Journal Of Photochemistry And Photobiology 日期:2015 卷标:152 页码:58-62]

    93-58-3 = 93-98-1
    反应条件:1.1 Catalysts: Phosphoric Acid,Aluminum Iron Salt; 4 H,92 °C
    标题:Mesoporous Iron Aluminophosphate: An Efficient Catalyst For One Pot Synthesis Of Amides By Ester-Amide Exchange Reaction
    作者:Vijayasankar,A. V.; Kathyayini,H.; Tumma,Harikrishna; Nagaraju,N.
    参考文献:Ceramic Transactions 日期:2012 卷标:233 页码:127-140]

    591-50-4 + 55-21-0 = 93-98-1
    反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: N,N′-Dimethylethylenediamine,Cuprous Iodide Solvents: Dimethyl Sulfoxide; 24 H,50 °C1.2 Reagents: Ethyl Acetate
    标题:Orthogonal Discrimination Among Functional Groups In Ullmann-Type C-O And C-N Couplings
    作者:Rovira,Mireia; Soler,Marta; Guell,Imma; Wang,Ming-Zheng; Gomez,Laura; Et Al
    参考文献:Journal Of Organic Chemistry 日期:2016 卷标:81(17) 页码:7315-7325]

    65-85-0 = 93-98-1
    反应条件:1.1 Reagents: Lithium Hydroxide,Oxygen Catalysts: Gold (Mesoporous Alumina-Supported) Solvents: Water; 14 H,Rt
    标题:Efficient Synthesis Of Amides And Esters From Alcohols Under Aerobic Ambient Conditions Catalyzed By A Au/mesoporous Al2O3 Nanocatalyst
    作者:Chng,Leng Leng; Yang,Jinhua; Ying,Jackie Y.
    参考文献:Chemsuschem 日期:2015 卷标:8(11) 页码:1916-1925]

    98-88-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Solvents: Tetrahydrofuran; 0 °C; 2 - 6 H,Rt
    标题:Innovative Strategy Toward Mutant Cftr Rescue In Cystic Fibrosis: Design And Synthesis Of Thiadiazole Inhibitors Of The E3 Ligase Rnf5
    作者:Brusa,Irene; Sondo,Elvira; Pesce,Emanuela; Tomati,Valeria; Gioia,Dario; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2023 卷标:66(14) 页码:9797-9822]

    7702-38-7 = 93-98-1
    反应条件:1.1 Reagents: Sodium Formate Solvents: Dimethyl Sulfoxide; 1 H,120 °C
    标题:Reductive Hydrodehalogenation Of Halogenated Carboxylic Acid Derivatives Using A Dmso/hcoona.2H2O System
    作者:Liu,Guyue; Hao,Feiyue; Liang,Lingling; Jin,Zhengneng; Wu,Jiashou
    参考文献:Organic Letters 日期:2023 卷标:25(15) 页码:2691-2695]

    591-50-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine,1,8-Diazabicyclo[5.4.0]Undec-7-Ene Catalysts: 2211997-02-1 (Silica Supported; Reaction Product With Pd2(Dba)3.CHCL3) Solvents: Dimethylformamide,Toluene; 3 H,30 Bar,100 °C
    标题:Double Carbonylation Of Iodoarenes In The Presence Of Reusable Palladium Catalysts Immobilised On Supported Phosphonium Ionic Liquid Phases
    作者:Urban,Bela; Szabo,Peter; Sranko,David; Safran,Gyorgy; Kollar,Laszlo; Et Al
    参考文献:Molecular Catalysis 日期:2018 卷标:445 页码:195-205]

    1548-84-1 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Solvents: Dimethylformamide; 16 H,100 °C
    标题:A Cross-Coupling Approach To Amide Bond Formation From Esters
    作者:Ben Halima,Taoufik; Vandavasi,Jaya Kishore; Shkoor,Mohanad; Newman,Stephen G.
    参考文献:Acs Catalysis 日期:2017 卷标:7(3) 页码:2176-2180]

    = 93-98-1
    反应条件:1.1 Catalysts: Acetic Anhydride
    标题:Acetic Anhydride
    作者:Zibuck,Regina
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001 卷标:1 页码:1-8]

    98-88-4 = 93-98-1
    反应条件:1.1 Reagents: Triethylamine Solvents: Dichloromethane; 0 °C; 0 °C -> Rt; 16 H,Rt1.2 Reagents: Water; Rt
    标题:Oxidative Fluorination Of N-Arylsulfonamides
    作者:Buckingham,Faye; Calderwood,Samuel; Checa,Begona; Keller,Thomas; Tredwell,Matthew; Et Al
    参考文献:Journal Of Fluorine Chemistry 日期:2015 卷标:180 页码:33-39
N-苄叉苯胺置于吡啶,甲醇,Oxone||potassium Monopersulfate Triple Salt,Copper(II) Oxide体系中,用32 %的收率获得产物n-苯甲酰替苯胺
参考文献:铜促进的亚胺氧化酰胺化:一种简便的酰胺化途径
标题:铜促进的亚胺氧化酰胺化:一种简便的酰胺化途径
摘要:开发了一种以醛和胺为原料,亚胺氧化制备酰胺的方法.以氧化铜为催化剂,Oxone为氧化剂,不使用任何偶联剂,反应条件温和.包括农药和药物分子在内的多种底物已被证明具有 32-90% 的产率.
DOI:10.1002/ejoc.202400315

海关参考信息

专利信息


专利号:WO-2024013769-A1
优先权日:2022-07-12
标题:Process for solvent free continuous synthesis of amides and peptides
发明人:KULKARNI AMOL ARVINDRAO; ATAPALKAR RANJIT SHABU
权利人:COUNCIL SCIENT IND RES
摘要:The present invention relates to a novel process for the solvent free continuous synthesis of amides and peptides. More particularly, the invention relates to a process for synthesizing amides and peptides using coupling reagents where the process is done at room temperature with lower residence time and solvent free synthesis, producing enhanced yields and purity products.

专利号:US-8735586-B2
优先权日:2007-06-26
标 题 :Regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR
权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR; SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

专利号:US-8188282-B2
优先权日:2006-07-15
标 题:Regioselective palladium catalyzed synthesis of benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; HALLAND NIS; RKYEK OMAR; URMANN MATTHIAS
权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; HALLAND NIS; RKYEK OMAR; URMANN MATTHIAS; SANOFI AVENTIS
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct palladium catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.

专利号:US-8124790-B2
优先权日:2008-01-02
标题:Preparation process useful in synthesis of atorvastatin
发明人:CHO DONG-OCK; KWON YOUNJA; CHA KYEONG-HOI; KIM YEONGSOOK; TAE HYUN-SEOP
权利人:CHO DONG-OCK; KWON YOUNJA; CHA KYEONG-HOI; KIM YEONGSOOK; TAE HYUN-SEOP; MEDICHEM KOREA CO LTD
摘要:The present invention relates to a preparation process useful in synthesis of atorvastatin, more particularly a process for preparing atorvastatin is effective in treating hyperlipemia, comprising protecting the dihydroxy group at C3 and C5 positions of the starting material cis-t-butyl-6-substituted-3,5-dihydroxy-hexanoate with trialkyl orthoformate, reducing the terminal nitro or cyano group to amine group, performing JV-alkylation by sequentially reacting with ethyl 4-fluorobenzene-2-haloacetate and isobutyryl chloride, cyclizing with JV,3-diphenylpropynamide, and performing deprotection and hydrolysis.

专利号:US-6765117-B2
优先权日:1997-10-24
标题:Process for stereoselective synthesis of prostacyclin derivatives
发明人:MORIARTY ROBERT M; PENMASTA RAJU; GUO LIANG; RAO MUNAGALA S; STASZEWSKI JAMES P
权利人:UNITED THERAPEUTIC CORP
摘要:An improved method is described for making 9-deoxy-PGF 1 -type compounds. In contrast to the prior art, the method is stereoselective and requires fewer steps than the known methods for making these compounds. The invention also relates to novel intermediates prepared during the synthesis of the 9-deoxy-PGF 1 -type compounds.

专利号:US-9656927-B2
优先权日:2013-11-01
标题 :Process for the synthesis of carboxylic acid derivatives
发明人:KISHORE PRASAD PRAGATI; SUDALAI ARUMUGAM
权利人:COUNCIL SCIENT IND RES; COUNCIL SCIENT IND RES
摘要:The present invention discloses one-pot synthesis of various carboxylic acid derivatives using copper catalyst and sodium cyanide as the cyanide source for bringing in carbonylative coupling in a single step.
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合成参考文献


摘要:Wu, X.-F., Science of Synthesis Knowledge Updates, (2014) 1, 302.
摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 281.
摘要:Silva, V. L. M.; Pinto, D. C. G. A.; Santos, C. M. M.; Rocha, D. H. A., Science of Synthesis Knowledge Updates, (2022) 3, 308.
摘要:Glushkov, V. A.; Shklyaev, Yu. V., Science of Synthesis Knowledge Updates, (2018) 3, 251.
摘要:Kang, F.-A.; Yang, S.-M., Science of Synthesis Knowledge Updates, (2015) 2, 216.
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