Kabachnik–Fields Reaction by Mechanochemistry: New Horizons from Old Methods

.  -Aminophosphonates are an important class of biologically active compounds, attracting considerable attention in medicinal chemistry, by inhibiting enzymes involved in amino acid metabolism. Herein, the Kabachnik-Fields domino reaction was investigated by mechanochemistry for the first-time preparation of  -aminophosphonate derivatives in high yields and with full selectivity, outperforming comparable solution procedures. The reaction occurs without the addition of any external catalyst, possibly via a metal-mediated process occurring on the surface of jar (zirconium oxide was used as the milling media). The mechanism of the mechanochemical reaction was also investigated by in situ Raman spectroscopy, the kinetic behavior was disclosed. The solid-state structures of two representative compounds have been determined by single-crystal X-ray diffractions.  Aminophosphonates were prepared by mechanochemical Kabachnick-Fields domino reaction and fully characterized at the solid state. The reaction mechanism and the kinetics were disclosed.

[1]  F. Delogu,et al.  Kinetics of mechanochemical transformations. , 2020, Physical chemistry chemical physics : PCCP.

[2]  F. Delogu,et al.  Metal-Mediated and Metal-Catalyzed Reactions Under Mechanochemical Conditions , 2020, ACS Catalysis.

[3]  M. Baláž,et al.  European Research in Focus: Mechanochemistry for Sustainable Industry (COST Action MechSustInd ) , 2020 .

[4]  H. Titi,et al.  Mechanochemistry for Synthesis. , 2019, Angewandte Chemie.

[5]  M. Etter,et al.  Direct Mechanocatalysis: Palladium as Milling Media and Catalyst in the Mechanochemical Suzuki Polymerization , 2019, Angewandte Chemie.

[6]  Francesco Delogu,et al.  From enabling technologies to medicinal mechanochemistry: an eco-friendly access to hydantoin-based active pharmaceutical ingredients , 2019, Reaction Chemistry & Engineering.

[7]  T. Friščić,et al.  Introducing Students to Mechanochemistry via Environmentally Friendly Organic Synthesis Using a Solvent-Free Mechanochemical Preparation of the Antidiabetic Drug Tolbutamide , 2019, Journal of Chemical Education.

[8]  G. Keglevich,et al.  Synthesis of phosphonates in a continuous flow manner , 2019, Phosphorus, Sulfur, and Silicon and the Related Elements.

[9]  G. Keglevich,et al.  The typical crystal structures of a few representative α-aryl-α-hydroxyphosphonates. , 2019, Acta crystallographica. Section C, Structural chemistry.

[10]  G. Keglevich,et al.  Continuous flow synthesis of α-aryl-α-aminophosphonates , 2018, Pure and Applied Chemistry.

[11]  P. Ricci,et al.  Processing and Investigation Methods in Mechanochemical Kinetics , 2018, ACS omega.

[12]  M. Mirzaei,et al.  Investigation of non-covalent and hydrogen bonding interactions on the formation of crystalline networks and supramolecular synthons of a series of α-aminophosphonates: Crystallography and DFT studies , 2018 .

[13]  G. Keglevich,et al.  Microwave irradiation and catalysis in organophosphorus reactions , 2018, Pure and Applied Chemistry.

[14]  Julie B. Zimmerman,et al.  The Green ChemisTREE: 20 years after taking root with the 12 principles , 2018 .

[15]  J. Mack,et al.  Recyclable heterogeneous metal foil-catalyzed cyclopropenation of alkynes and diazoacetates under solvent-free mechanochemical reaction conditions† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc00443a , 2018, Chemical science.

[16]  E. Bálint,et al.  Synthesis of α-aminophosphonates by the Kabachnik–Fields reaction and by the Pudovik reaction , 2018 .

[17]  D. Browne,et al.  Mechanochemistry as an emerging tool for molecular synthesis: what can it offer? , 2018, Chemical science.

[18]  Marco Leonardi,et al.  Multicomponent mechanochemical synthesis , 2018, Chemical science.

[19]  G. Keglevich,et al.  Advantages of the Microwave Tool in Organophosphorus Syntheses , 2017, Synthesis.

[20]  William Jones,et al.  Screening for new pharmaceutical solid forms using mechanochemistry: A practical guide☆ , 2017, Advanced drug delivery reviews.

[21]  Jean Martínez,et al.  N-Acyl Benzotriazole Derivatives for the Synthesis of Dipeptides and Tripeptides and Peptide Biotinylation by Mechanochemistry , 2017 .

[22]  Jean Martínez,et al.  Sonochemistry in non-conventional, green solvents or solvent-free reactions , 2017 .

[23]  Y. Békro,et al.  5-H-1,2-Oxaphosphole 2-oxides, key building blocks for diversity oriented chemical libraries , 2016 .

[24]  Jun-jie Wang,et al.  Manganese(III) Acetate‐Promoted Cross‐Coupling Reaction of Benzothiazole/Thiazole Derivatives with Organophosphorus Compounds under Ball‐Milling Conditions. , 2016 .

[25]  Jean Martínez,et al.  Mechanochemical Preparation of 3,5-Disubstituted Hydantoins from Dipeptides and Unsymmetrical Ureas of Amino Acid Derivatives. , 2016, The Journal of organic chemistry.

[26]  W. Gao,et al.  Synthesis, X-Ray Crystallographic Analysis and BSA Interaction of a New α-Aminophosphonate , 2016 .

[27]  G. Keglevich,et al.  Synthesis of α-aminophosphonates from α-hydroxyphosphonates; a theoretical study , 2016 .

[28]  Davin Tan,et al.  Towards medicinal mechanochemistry: evolution of milling from pharmaceutical solid form screening to the synthesis of active pharmaceutical ingredients (APIs). , 2016, Chemical communications.

[29]  Jean Martínez,et al.  Poly(ethylene) glycols and mechanochemistry for the preparation of bioactive 3,5-disubstituted hydantoins , 2016 .

[30]  James Mack,et al.  Nickel Catalysis in a High Speed Ball Mill: A Recyclable Mechanochemical Method for Producing Substituted Cyclooctatetraene Compounds , 2016 .

[31]  T. Hanusa,et al.  Advances in organometallic synthesis with mechanochemical methods. , 2016, Dalton transactions.

[32]  Jean Martínez,et al.  Mechanochemical 1,1′-Carbonyldiimidazole-Mediated Synthesis of Carbamates , 2015 .

[33]  K. Bijak,et al.  Optical and electrochemical properties of novel thermally stable Schiff bases bearing naphthalene unit , 2015 .

[34]  T. Ali,et al.  Methods for the Synthesis of α‐Heterocyclic/Heteroaryl‐α‐Aminophosphonic Acids and Their Esters , 2015 .

[35]  Amanda B Maginty,et al.  Nucleoside Azide–Alkyne Cycloaddition Reactions Under Solvothermal Conditions or Using Copper Vials in a Ball Mill , 2015, Nucleosides, nucleotides & nucleic acids.

[36]  Mei-Xiang Wang,et al.  Multicomponent reactions in organic synthesis , 2014 .

[37]  K. Suslick Mechanochemistry and sonochemistry: concluding remarks. , 2014, Faraday discussions.

[38]  Jean Martínez,et al.  Mechanochemical preparation of hydantoins from amino esters: application to the synthesis of the antiepileptic drug phenytoin. , 2014, The Journal of organic chemistry.

[39]  G. Keglevich,et al.  A Critical Overview of the Kabachnik–Fields Reactions Utilizing Trialkyl Phosphites in Water as the Reaction Medium: A Study of the Benzaldehyde‐Benzylamine Triethyl Phosphite/Diethyl Phosphite Models , 2014 .

[40]  Tomislav Friščić,et al.  Laboratory real-time and in situ monitoring of mechanochemical milling reactions by Raman spectroscopy. , 2014, Angewandte Chemie.

[41]  Magnus Rueping,et al.  Catalytic C-C bond-forming multi-component cascade or domino reactions: pushing the boundaries of complexity in asymmetric organocatalysis. , 2014, Chemical reviews.

[42]  S. Yin,et al.  Air-stable zirconocene bis(perfluorobutanesulfonate) as a highly efficient catalyst for synthesis of α-aminophosphonates via Kabachnik–Fields reaction under solvent-free condition , 2014 .

[43]  Müller Third Component Phosphonate (Kabachnik–Fields Reaction) , 2014 .

[44]  R. Luque,et al.  Solvent-free and catalysts-free chemistry: a benign pathway to sustainability. , 2014, ChemSusChem.

[45]  Jean Martínez,et al.  Solventless Synthesis of N-Protected Amino Acids in a Ball Mill , 2013 .

[46]  P. R. Sharma,et al.  Grinding-induced rapid, convenient and solvent free approach for the one pot synthesis of α-aminophosphonates using aluminium pillared interlayered clay catalyst , 2013 .

[47]  James Mack,et al.  Scratching the catalytic surface of mechanochemistry: a multi-component CuAAC reaction using a copper reaction vial , 2013 .

[48]  Tomislav Friščić,et al.  Real-time and in situ monitoring of mechanochemical milling reactions. , 2013, Nature chemistry.

[49]  G. Keglevich,et al.  The Kabachnik–Fields Reaction: Mechanism and Synthetic Use , 2012, Molecules.

[50]  M. Gray,et al.  Incorporation of steroidal biomarkers into petroleum model compounds , 2012 .

[51]  G. Cravotto,et al.  Harnessing mechanochemical effects with ultrasound-induced reactions , 2012 .

[52]  James Mack,et al.  Mechanochemistry: opportunities for new and cleaner synthesis. , 2012, Chemical Society reviews.

[53]  Yufen Zhao,et al.  Copper (I) Iodide-Catalyzed Solvent-Free Synthesis of α-Aminophosphonates , 2011 .

[54]  G. Keglevich,et al.  Microwave‐Assisted Synthesis of α‐Hydroxybenzylphosphonates and ‐benzylphosphine Oxides. , 2011 .

[55]  Zhi‐Hua Yu,et al.  Synthesis, Crystal Structure, and Herbicidal Activity of Pyrimidinyl Benzylamine Analogues Containing a Phosphonyl Group. , 2010 .

[56]  M. Garland,et al.  On the Tautomerism of Secondary Phosphane Oxides , 2010 .

[57]  L. I. Minaeva,et al.  Catalytic synthesis of α-hydroxyphosphonates , 2009 .

[58]  Anna Szekrényi,et al.  Eco‐Friendly Accomplishment of the Extended Kabachnik—Fields Reaction; a Solvent‐ and Catalyst‐Free Microwave‐Assisted Synthesis of α‐Aminophosphonates and α‐Aminophosphine Oxides. , 2009 .

[59]  M. G. Babashkina,et al.  Synthesis of a new α-aminophosphonate library. Crystal structure of p-XC6H4–NH–CH(p-BrC6H4)–P(O)(OiPr)2 (X = H, Br, CH3O) , 2009 .

[60]  A. Chakraborti,et al.  Zirconium(IV) compounds as efficient catalysts for synthesis of alpha-aminophosphonates. , 2008, The Journal of organic chemistry.

[61]  N. Zefirov,et al.  On the mechanism of the Kabachnik-Fields reaction: Does a mechanism of nucleophilic amination of α-hydroxyphosphonates exist? , 2008 .

[62]  N. S. Zefirov,et al.  Catalytic Kabachnik-Fields reaction: new horizons for old reaction , 2008 .

[63]  M. Xia,et al.  Ultrasound-assisted one-pot approach to alpha-amino phosphonates under solvent-free and catalyst-free conditions. , 2007, Ultrasonics sonochemistry.

[64]  N. Iranpoor,et al.  Metal Triflate Catalyzed One‐Pot Synthesis of α‐Aminophosphonates from Carbonyl Compounds in the Absence of Solvent. , 2005 .

[65]  A. Manjula,et al.  One-Pot Synthesis of α-Aminophosphonates: An Inexpensive Approach , 2003 .

[66]  T. James,et al.  Saccharide-accelerated hydrolysis of boronic acid imines , 2002 .

[67]  Frank H. Allen,et al.  Cambridge Structural Database , 2002 .

[68]  J. Yadav,et al.  Zr4+‐Catalyzed Efficient Synthesis of α‐Aminophosphonates. , 2002 .

[69]  S. Price,et al.  Dimer or catemer? Low-energy crystal packings for small carboxylic acids , 2000 .

[70]  R. Cherkasov,et al.  The Kabachnik–Fields reaction: synthetic potential and the problem of the mechanism , 1998 .

[71]  E. LaVoie,et al.  Bioisosterism: A Rational Approach in Drug Design. , 1996, Chemical reviews.

[72]  P. Moles Zirconium-based coupling agents and adhesion promoters , 1992 .

[73]  C. Blaise,et al.  Zirconium toxicity assessment using bacteria, algae and fish assays , 1989 .

[74]  B. Kojić-Prodić,et al.  dl-Diethyl α-anilinobenzylphosphonate , 1978 .

[75]  V. Jagodić INFRARED SPECTRA OF ORGANOPHOSPHORUS COMPOUNDS. III , 1977 .

[76]  V. Jagodić SYNTHESIS AND BASIC HYDROLYSIS OF DIESTERS OF α‐ANILINOBENZYLPHOSPHONIC ACID. CONFORMATIONAL STUDY OF ESTERS BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY , 1977 .

[77]  L. Orgel,et al.  Mechanism of Enzyme Inhibition by Phosphate Esters , 1959, Science.

[78]  Ellis K. Fields,et al.  The Synthesis of Esters of Substituted Amino Phosphonic Acids1a , 1952 .