Water mediated chemoselective synthesis of 1,2-disubstituted benzimidazoles using o-phenylenediamine and the extended synthesis of quinoxalines

By applying water as the reaction medium, the one-pot synthesis of 1,2-disubstituted benzimidazoles has been achieved in excellent efficiency and selectivity at room temperature viatrimethylsilyl chloride promoted reaction of o-phenylenediamine with aldehyde. This green catalyst system has also been successfully extended to the synthesis of quinoxalines via the reaction of o-phenylenediamine with α-bromoketone. Water displayed a specific functionality in mediating the selectivity, and remarkable advantages over organic solvents in terms of yields as well as in the work up procedure of the reactions.

[1]  B. Ranu,et al.  Remarkable influence of substituent in ionic liquid in control of reaction: simple, efficient and hazardous organic solvent free procedure for the synthesis of 2-aryl benzimidazoles promoted by ionic liquid, [pmim]BF4 , 2009 .

[2]  Jie‐Ping Wan,et al.  Chemo-/regioselective synthesis of 6-unsubstituted dihydropyrimidinones, 1,3-thiazines and chromones via novel variants of Biginelli reaction. , 2009, Chemical communications.

[3]  Jie‐Ping Wan,et al.  Novel regioselectivity: three-component cascade synthesis of unsymmetrical 1,4- and 1,2-dihydropyridines. , 2009, The Journal of organic chemistry.

[4]  A. Wu,et al.  A new diastereoselective multicomponent, one-pot strategy for the synthesis of 3-substituted isoindolinones via efficient C–C bond formation , 2008 .

[5]  Wei Zhang,et al.  Efficient aerobic oxidative synthesis of 2-substituted benzoxazoles, benzothiazoles, and benzimidazoles catalyzed by 4-methoxy-TEMPO. , 2008, Angewandte Chemie.

[6]  H. Sharghi,et al.  Reusable Cobalt(III)‐Salen Complex Supported on Activated Carbon as an Efficient Heterogeneous Catalyst for Synthesis of 2‐Arylbenzimidazole Derivatives , 2008 .

[7]  S. Suib,et al.  Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines , 2008 .

[8]  H. Iwaasa,et al.  Design, syntheses, and structure-activity relationships of novel NPY Y5 receptor antagonists: 2-{3-Oxospiro[isobenzofuran-1(3H),4'-piperidin]-1'-yl}benzimidazole derivatives. , 2008, Bioorganic & medicinal chemistry letters.

[9]  Mikhail Nikulnikov,et al.  Poorly reactive 5-piperazin-1-yl-1,3,4-thiadiazol-2-amines rendered as valid substrates for Groebke–Blackburn type multi-component reaction with aldehydes and isocyanides using TMSCl as a promoter , 2008 .

[10]  Y. Bansal,et al.  Angiotensin II--AT1 receptor antagonists: design, synthesis and evaluation of substituted carboxamido benzimidazole derivatives. , 2008, European journal of medicinal chemistry.

[11]  S. Bhattacharya,et al.  Medical implications of benzimidazole derivatives as drugs designed for targeting DNA and DNA associated processes. , 2008, Current medicinal chemistry.

[12]  K. Bahrami,et al.  Mild and highly efficient method for the synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles. , 2008, The Journal of organic chemistry.

[13]  B. Sreedhar,et al.  FeCl3/TMSCl:An Effective Catalytic System for the Conjugate Addition of Sodium p-Toluenesulfinate to α,β-Enones , 2008 .

[14]  Eric F. Johnson,et al.  Synthesis and SAR of novel, potent and orally bioavailable benzimidazole inhibitors of poly(ADP-ribose) polymerase (PARP) with a quaternary methylene-amino substituent. , 2008, Bioorganic & medicinal chemistry letters.

[15]  K. S. Shankar,et al.  Bismuth(III)-catalyzed rapid and highly efficient synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles in water , 2008 .

[16]  C. Cho,et al.  Copper-catalyzed oxidative cyclization of α-hydroxyketones with o-phenylenediamines leading to quinoxalines , 2007 .

[17]  Y. Harigaya,et al.  Tosic Acid-on-Silica Gel: A Cheap and Eco-friendly Catalyst for a Convenient One-pot Synthesis of Substituted Benzimidazoles , 2007 .

[18]  E. Ramu,et al.  Zn-proline catalyzed selective synthesis of 1,2-disubstituted benzimidazoles in water. , 2007, Chemical & pharmaceutical bulletin.

[19]  B. Das,et al.  An efficient and convenient protocol for the synthesis of quinoxalines and dihydropyrazines via cyclization–oxidation processes using HClO4·SiO2 as a heterogeneous recyclable catalyst ☆ , 2007 .

[20]  K. Bahrami,et al.  A Simple and Efficient One-Pot Synthesis of 2-Substituted Benzimidazoles , 2007 .

[21]  C. Yao,et al.  Cerium (IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient and green approach for the synthesis of quinoxalines , 2006 .

[22]  C. Cho,et al.  A new ruthenium-catalyzed approach for quinoxalines from o-phenylenediamines and vicinal-diols , 2006 .

[23]  A. Wu,et al.  Two novel diastereoselective three-component reactions of alkenes or 3,4-dihydro-(2H)-pyran with urea/thiourea-aldehyde mixtures: [4 + 2] cycloaddition vs Biginelli-type reaction. , 2006, Organic letters.

[24]  M. Zolfigol,et al.  Selective synthesis of 2-aryl-1-arylmethyl-1H-1,3-benzimidazoles in water at ambient temperature , 2006 .

[25]  A. Iwashita,et al.  Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling. , 2006, Bioorganic & medicinal chemistry.

[26]  R. Gibbs,et al.  A convenient one-pot synthesis of 2-substituted benzimidazoles , 2006 .

[27]  Mercedes González,et al.  Imidazole and benzimidazole derivatives as chemotherapeutic agents. , 2005, Mini reviews in medicinal chemistry.

[28]  K. Park,et al.  Manganese(IV) dioxide-catalyzed synthesis of quinoxalines under microwave irradiation. , 2005, Chemical communications.

[29]  A. Brukštus,et al.  Synthesis and Antiinflammatory Activity of Some New 1-Acyl Derivatives of 2-Methylthio-5,6-Diethoxybenzimidazole , 2004, Pharmaceutical Chemistry Journal.

[30]  C. Lindsley,et al.  General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines , 2004 .

[31]  C. Xia,et al.  Highly efficient phosphine-catalyzed aza-Michael reactions of α,β-unsaturated compounds with carbamates in the presence of TMSCl , 2004 .

[32]  C. D. Wilfred,et al.  Tandem oxidation processes for the preparation of nitrogen-containing heteroaromatic and heterocyclic compounds. , 2004, Organic & biomolecular chemistry.

[33]  C. D. Wilfred,et al.  Preparation of quinoxalines, dihydropyrazines, pyrazines and piperazines using tandem oxidation processes. , 2003, Chemical communications.

[34]  P. Beaulieu,et al.  A Practical Oxone®-Mediated, High-Throughput, Solution-Phase Synthesis of Benzimidazoles from 1,2-Phenylenediamines and Aldehydes and its Application to Preparative Scale Synthesis , 2003 .

[35]  A. J. Blake,et al.  Synthesis of benzimidazoles in high-temperature water , 2003 .

[36]  Douglas A. Horton,et al.  The combinatorial synthesis of bicyclic privileged structures or privileged substructures. , 2003, Chemical reviews.

[37]  S. Ioffe,et al.  Carbon-carbon bond forming reactions mediated by silicon Lewis acids. , 2003, Chemical reviews.

[38]  R. Reynolds,et al.  Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives. , 2002, Journal of medicinal chemistry.

[39]  V. Lynch,et al.  Quinoxaline-bridged porphyrinoids. , 2002, Journal of the American Chemical Society.

[40]  Rajkumar J. Sevak,et al.  GASTROPROTECTIVE EFFECT OF β3 ADRENOCEPTOR AGONISTS ZD 7114 AND CGP 12177A IN RATS , 2002 .

[41]  D. M. Boghaei,et al.  Non-symmetrical tetradentate vanadyl Schiff base complexes derived from 1,2-phenylene diamine and 1,3-naphthalene diamine as catalysts for the oxidation of cyclohexene , 2002 .

[42]  S. Antoniotti,et al.  Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines , 2002 .

[43]  B. Ganem,et al.  Metal-promoted variants of the Passerini reaction leading to functionalized heterocycles. , 2002, Organic letters.

[44]  C. Brain,et al.  An intramolecular palladium-catalysed aryl amination reaction to produce benzimidazoles , 2002 .

[45]  L. Scott,et al.  Esomeprazole , 2012, Drugs.

[46]  I. Sage,et al.  Synthesis and device characterisation of side-chain polymer electron transport materials for organic semiconductor applications , 2001 .

[47]  P. Rea,et al.  ‘One-pot’ nitro reduction–cyclisation solid phase route to benzimidazoles , 2000 .

[48]  E. Buyukbingol,et al.  A study on the antioxidant capacities of some benzimidazoles in rat tissues. , 1998, Chemico-biological interactions.

[49]  H. Al-Muhaimeed A Parallel-Group Comparison of Astemizole and Loratadine for the Treatment of Perennial Allergic Rhinitis , 1997, The Journal of international medical research.

[50]  G. Mcmahon,et al.  Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins. , 1996, Journal of medicinal chemistry.

[51]  A. Benazzouz,et al.  Riluzole prevents MPTP-induced parkinsonism in the rhesus monkey: a pilot study. , 1995, European journal of pharmacology.

[52]  R. Perry,et al.  A novel palladium-catalyzed synthesis of 2-arylbenzimidazoles , 1993 .

[53]  W. R. Jackson,et al.  Synthesis of benzimidazoles containing a fused alicyclic ring by Rhodium - catalysed hydroformylation of N-alkenyl-1,2-diaminobenzenes , 1992 .

[54]  R. G. Browne,et al.  4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. , 1990, Journal of medicinal chemistry.

[55]  W. Denny,et al.  Potential antitumor agents. 59. Structure-activity relationships for 2-phenylbenzimidazole-4-carboxamides, a new class of "minimal" DNA-intercalating agents which may not act via topoisomerase II. , 1990, Journal of medicinal chemistry.

[56]  P. N. Preston,et al.  Synthesis, reactions, and spectroscopic properties of benzimidazoles , 1974 .