Click chemistry reactions in medicinal chemistry: Applications of the 1,3‐dipolar cycloaddition between azides and alkynes

In recent years, there has been an ever‐increasing need for rapid reactions that meet the three main criteria of an ideal synthesis: efficiency, versatility, and selectivity. Such reactions would allow medicinal chemistry to keep pace with the multitude of information derived from modern biological screening techniques. The present review describes one of these reactions, the 1,3‐dipolar cycloaddition (“click‐reaction”) between azides and alkynes catalyzed by copper (I) salts. The simplicity of this reaction and the ease of purification of the resulting products have opened new opportunities in generating vast arrays of compounds with biological potential. The present review will outline the accomplishments of this strategy achieved so far and outline some of medicinal chemistry applications in which click‐chemistry might be relevant in the future. © 2007 Wiley Periodicals, Inc. Med Res Rev, 28, No. 2, 278–308, 2008

[1]  K. Sharpless,et al.  Direct synthesis of 1,5-disubstituted-4-magnesio-1,2,3-triazoles, revisited. , 2004, Organic letters.

[2]  R. Fisher,et al.  Application of azide-alkyne cycloaddition 'click chemistry' for the synthesis of Grb2 SH2 domain-binding macrocycles. , 2006, Bioorganic & medicinal chemistry letters.

[3]  Wen‐Shan Li,et al.  Lithocholic acid analogues, new and potent α-2,3-sialyltransferase inhibitors , 2006 .

[4]  Sachiko Sato,et al.  Carbohydrate triazoles and isoxazoles as inhibitors of galectins-1 and -3. , 2006, Chemical communications.

[5]  Sanghee Kim,et al.  Synthesis and Evaluation of 1,2,3-Triazole Containing Analogues of the Immunostimulant α-GalCer , 2007 .

[6]  C. B. Naylor,et al.  Synthesis and muscarinic activities of quinuclidin-3-yltriazole and -tetrazole derivatives. , 1992, Journal of medicinal chemistry.

[7]  Luke G Green,et al.  A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.

[8]  F. Matsumura,et al.  Synthesis and structure-activity relationships of 1-phenyl-1H-1,2,3-triazoles as selective insect GABA receptor antagonists. , 2006, Journal of agricultural and food chemistry.

[9]  D. Leigh,et al.  Chemoselective formation of successive triazole linkages in one pot: "click-click" chemistry. , 2006, Organic letters.

[10]  S. Schreiber,et al.  Macrocycloadditions leading to conformationally restricted small molecules. , 2006, Organic letters.

[11]  C. Hawker,et al.  Structurally diverse dendritic libraries : A highly efficient functionalization approach using Click chemistry , 2005 .

[12]  N. F. Osborne,et al.  6-(SUBSTITUTED METHYLENE)PENEMS, POTENT BROAD SPECTRUM INHIBITORS OF BACTERIAL β-LACTAMASE , 1991 .

[13]  Jean-François Lutz,et al.  1,3-dipolar cycloadditions of azides and alkynes: a universal ligation tool in polymer and materials science. , 2007, Angewandte Chemie.

[14]  P. Gmeiner,et al.  Click chemistry on solid phase: parallel synthesis of N-benzyltriazole carboxamides as super-potent G-protein coupled receptor ligands. , 2006, Journal of combinatorial chemistry.

[15]  Kalyan C. Tirupula,et al.  Click Chemistry on Azidoproline: High‐Affinity Dual Antagonist for HIV‐1 Envelope Glycoprotein gp120 , 2006, ChemMedChem.

[16]  C. Seto,et al.  A two stage click-based library of protein tyrosine phosphatase inhibitors. , 2007, Bioorganic & medicinal chemistry.

[17]  Yuguo Du,et al.  A practical synthesis of a (1→6)-linked β-d-glucosamine nonasaccharide , 2003 .

[18]  F. Sasse,et al.  Synthesis of a Benzolactone Collection using Click Chemistry , 2007 .

[19]  Spencer J. Williams,et al.  Use of Click Chemistry to Define the Substrate Specificity of Leishmania β‐1,2‐Mannosyltransferases , 2006, Chembiochem : a European journal of chemical biology.

[20]  P. Taylor,et al.  Click chemistry in situ: acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks. , 2002, Angewandte Chemie.

[21]  S. Handy,et al.  Towards the Ideal Synthesis , 1998 .

[22]  I. Akritopoulou‐Zanze,et al.  A Versatile Synthesis of Fused Triazolo Derivatives by Sequential Ugi/Alkyne—Azide Cycloaddition Reactions. , 2005 .

[23]  Mahesh Uttamchandani,et al.  Rapid assembly and in situ screening of bidentate inhibitors of protein tyrosine phosphatases. , 2006, Organic letters.

[24]  (-)-FR182877 is a potent and selective inhibitor of carboxylesterase-1. , 2003, Angewandte Chemie.

[25]  Chun Xing Li,et al.  'Click chemistry' on polysaccharides: a convenient, general, and monitorable approach to develop (1-->3)-beta-D-glucans with various functional appendages. , 2005, Carbohydrate research.

[26]  M. Kaiser,et al.  Toward Semisynthetic Lipoproteins by Convergent Strategies Based on Click and Ligation Chemistry , 2005, Chembiochem : a European journal of chemical biology.

[27]  G. Marriott,et al.  Synthesis and characterization of the 7-(4-aminomethyl-1H-1,2,3-triazol-1-yl) analogue of kabiramide C. , 2005, Journal of natural products.

[28]  G. Lessene,et al.  Synthesis of azide-alkyne fragments for ‘click’ chemical applications; formation of oligomers from orthogonally protected trialkylsilyl-propargyl azides and propargyl alcohols , 2006 .

[29]  M. Ghadiri,et al.  Heterocyclic Peptide Backbone Modifications in an α-Helical Coiled Coil , 2004 .

[30]  M. Kume,et al.  Orally active cephalosporins. III. Synthesis and structure-activity relationships of new 3-heterocyclicthiomethylthio-7 beta-[(Z)- 2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-3-cephem-4 -carboxylic acids. , 1993, The Journal of antibiotics.

[31]  B. Lipshutz,et al.  Heterogeneous copper-in-charcoal-catalyzed click chemistry. , 2006, Angewandte Chemie.

[32]  K. Sharpless,et al.  Polytriazoles as copper(I)-stabilizing ligands in catalysis. , 2004, Organic letters.

[33]  C. Aldrich,et al.  Rationally designed nucleoside antibiotics that inhibit siderophore biosynthesis of Mycobacterium tuberculosis. , 2006, Journal of medicinal chemistry.

[34]  Günter Szeimies,et al.  1.3-Dipolare Cycloadditionen, XXXII. Kinetik der Additionen organischer Azide an CC-Mehrfachbindungen , 1967 .

[35]  B. Suh,et al.  Vitamin D side chain triazole analogs via cycloaddition `click' chemistry , 2004 .

[36]  F. Santoyo-González,et al.  Multivalent neoglycoconjugates by regiospecific cycloaddition of alkynes and azides using organic-soluble copper catalysts. , 2003, Organic letters.

[37]  J. Porco,et al.  Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by copper-catalyzed cycloaddition-coupling of azides and terminal alkynes , 2006 .

[38]  O. Makabe,et al.  SYNTHESES OF D‐ARABINOFURANOSYL AND 2′‐DEOXY‐D‐RIBOFURANOSYL 1,2,3‐TRIAZOLECARBOXAMIDES , 1977 .

[39]  D. Hlasta,et al.  Trimethylsilyl-directed 1,3-dipolar cycloaddition reactions in the solid-phase synthesis of 1,2,3-triazoles. , 2005, Organic letters.

[40]  E. Kool,et al.  Chemoselective covalent coupling of oligonucleotide probes to self-assembled monolayers. , 2005, Journal of the American Chemical Society.

[41]  Chi-Huey Wong,et al.  In situ click chemistry: enzyme-generated inhibitors of carbonic anhydrase II. , 2004, Angewandte Chemie.

[42]  William Lindstrom,et al.  Inhibitors of HIV-1 protease by using in situ click chemistry. , 2006, Angewandte Chemie.

[43]  Xue-Long Sun,et al.  Carbohydrate and protein immobilization onto solid surfaces by sequential Diels-Alder and azide-alkyne cycloadditions. , 2006, Bioconjugate chemistry.

[44]  H. Kolb,et al.  The growing impact of click chemistry on drug discovery. , 2003, Drug discovery today.

[45]  G. Tron,et al.  Rapid synthesis of triazole-modified resveratrol analogues via click chemistry. , 2006, Journal of medicinal chemistry.

[46]  S. Weinreb,et al.  β-Tosylethylazide: a useful synthon for preparation of N-protected 1,2,3-triazoles via click chemistry , 2006 .

[47]  Qian Wang,et al.  Bioconjugation by copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition. , 2003, Journal of the American Chemical Society.

[48]  G. H. Coombs,et al.  Combinatorial library of peptidotriazoles: identification of [1,2,3]-triazole inhibitors against a recombinant Leishmania mexicana cysteine protease. , 2004, Journal of combinatorial chemistry.

[49]  M. Kume,et al.  ORALLY ACTIVE CEPHALOSPORINS , 1993 .

[50]  Xumu Zhang,et al.  Triazole-based monophosphines for Suzuki-Miyaura coupling and amination reactions of aryl chlorides. , 2005, Organic letters.

[51]  Thomas Carell,et al.  Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA. , 2006, Organic letters.

[52]  S. Weinreb,et al.  A study of the scope and regioselectivity of the ruthenium-catalyzed [3 + 2]-cycloaddition of azides with internal alkynes. , 2006, The Journal of organic chemistry.

[53]  H. Hiemstra,et al.  CuI‐Catalyzed Alkyne—Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective , 2006 .

[54]  K. Kirshenbaum,et al.  Click to fit: versatile polyvalent display on a peptidomimetic scaffold. , 2005, Organic letters.

[55]  L. Moro,et al.  Estrogenic Analogues Synthesized by Click Chemistry , 2007, ChemMedChem.

[56]  D. Speijer,et al.  1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics. , 2007, Organic & biomolecular chemistry.

[57]  U. Nilsson,et al.  C2-symmetric macrocyclic carbohydrate/amino acid hybrids through copper(I)-catalyzed formation of 1,2,3-triazoles. , 2005, The Journal of organic chemistry.

[58]  D. Hlasta,et al.  Steric Effects on the Regioselectivity of an Azide-Alkyne Dipolar Cycloaddition Reaction: The Synthesis of Human Leukocyte Elastase Inhibitors. , 1995 .

[59]  C. Walsh,et al.  A chemoenzymatic approach to glycopeptide antibiotics. , 2004, Journal of the American Chemical Society.

[60]  M. Uttamchandani,et al.  Rapid assembly of matrix metalloprotease inhibitors using click chemistry. , 2006, Organic letters.

[61]  Anna E Speers,et al.  Profiling enzyme activities in vivo using click chemistry methods. , 2004, Chemistry & biology.

[62]  M. Finn,et al.  Accelerated bioorthogonal conjugation: a practical method for the ligation of diverse functional molecules to a polyvalent virus scaffold. , 2005, Bioconjugate chemistry.

[63]  S. Neidle,et al.  Stabilization of G-quadruplex DNA by highly selective ligands via click chemistry. , 2006, Journal of the American Chemical Society.

[64]  P. Arora,et al.  Nonpeptidic foldamers from amino acids: synthesis and characterization of 1,3-substituted triazole oligomers. , 2005, Journal of the American Chemical Society.

[65]  Q. Wang,et al.  A fluorogenic 1,3-dipolar cycloaddition reaction of 3-azidocoumarins and acetylenes. , 2004, Organic letters.

[66]  Yuguo Du,et al.  Synthesis of a C3-symmetric (1-->6)-N-acetyl-beta-D-glucosamine octadecasaccharide using click chemistry. , 2005, Carbohydrate research.

[67]  Ian D. Williams,et al.  Ruthenium-catalyzed cycloaddition of alkynes and organic azides. , 2006, Journal of the American Chemical Society.

[68]  J. Gawroński,et al.  THE LIBRARY OF CINCHONA ALKALOIDS-1,2,3-TRIAZOLE DERIVATIVES: STRUCTURE AND FACILE ACCESS BY "CLICK CHEMISTRY" , 2005 .

[69]  Zoran Radić,et al.  In situ click chemistry: enzyme inhibitors made to their own specifications. , 2004, Journal of the American Chemical Society.

[70]  C. K. Chu,et al.  Synthesis of cyclopentenyl carbocyclic nucleosides as potential antiviral agents against orthopoxviruses and SARS. , 2006, Journal of medicinal chemistry.

[71]  Weiliang Zhu,et al.  Syntheses of triazole-modified zanamivir analogues via click chemistry and anti-AIV activities. , 2006, Bioorganic & medicinal chemistry letters.

[72]  Chi-Huey Wong,et al.  A potent and highly selective inhibitor of human alpha-1,3-fucosyltransferase via click chemistry. , 2003, Journal of the American Chemical Society.

[73]  O. Makabe,et al.  Syntheses of D-Arabinofuranosyl and 2′-Deoxy-D-ribofuranosyl 1,2,3-Triazolecarboxamides , 1976 .

[74]  Doris Dallinger,et al.  Combining Biginelli multicomponent and click chemistry: generation of 6-(1,2,3-triazol-1-yl)-dihydropyrimidone libraries. , 2004, Journal of combinatorial chemistry.

[75]  M. Finn,et al.  "Clickable" agarose for affinity chromatography. , 2005, Bioconjugate chemistry.

[76]  K. Burgess,et al.  Ring Closure to β-Turn Mimics via Copper-Catalyzed Azide/Alkyne Cycloadditions , 2005 .

[77]  Chi‐Huey Wong,et al.  High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays. , 2004, Bioorganic & medicinal chemistry letters.

[78]  J. Thorson,et al.  Diversifying vancomycin via chemoenzymatic strategies. , 2005, Organic letters.

[79]  F. Santoyo-González,et al.  Synthesis of Glyco‐Silicas by Cu(I)‐Catalyzed “Click‐Chemistry” and their Applications in Affinity Chromatography , 2006 .

[80]  K. Bogeso,et al.  Bioisosteres of arecoline: 1,2,3,6-tetrahydro-5-pyridyl-substituted and 3-piperidyl-substituted derivatives of tetrazoles and 1,2,3-triazoles. Synthesis and muscarinic activity. , 1994, Journal of medicinal chemistry.

[81]  J. V. van Maarseveen,et al.  Click chemistry as a route to cyclic tetrapeptide analogues: synthesis of cyclo-[Pro-Val-psi(triazole)-Pro-Tyr]. , 2006, Organic letters.

[82]  Wolfgang H. Binder and Christian Kluger Azide/Alkyne-“Click” Reactions: Applications in Material Science and Organic Synthesis , 2006 .

[83]  K. Sharpless,et al.  In situ click chemistry: a powerful means for lead discovery , 2006, Expert opinion on drug discovery.

[84]  B. Westermann,et al.  A short route for the synthesis of "sweet" macrocycles via a click-dimerization-ring-closing metathesis approach. , 2005, Chemical communications.

[85]  S. Danishefsky,et al.  A potentially valuable advance in the synthesis of carbohydrate-based anticancer vaccines through extended cycloaddition chemistry. , 2006, The Journal of organic chemistry.

[86]  T. Kauffmann The Arenology Principle , 1971 .

[87]  Anna E Speers,et al.  Activity-based protein profiling in vivo using a copper(i)-catalyzed azide-alkyne [3 + 2] cycloaddition. , 2003, Journal of the American Chemical Society.

[88]  C. Barbas,et al.  Towards organo-click chemistry: development of organocatalytic multicomponent reactions through combinations of aldol, Wittig, Knoevenagel, Michael, Diels-Alder and Huisgen cycloaddition reactions. , 2004, Chemistry.

[89]  Craig J Hawker,et al.  Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(i)-catalyzed ligation of azides and alkynes. , 2004, Angewandte Chemie.

[90]  Morten Meldal,et al.  Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. , 2002, The Journal of organic chemistry.

[91]  Chi‐Huey Wong,et al.  A Potent and Highly Selective Inhibitor of Human α-1,3-Fucosyltransferase via Click Chemistry , 2003 .

[92]  G. Szakács,et al.  Discovery of a daunorubicin analogue that exhibits potent antitumor activity and overcomes P-gp-mediated drug resistance. , 2006, Journal of Medicinal Chemistry.

[93]  Anna E Speers,et al.  Chemical Strategies for Activity‐Based Proteomics , 2004, Chembiochem : a European journal of chemical biology.

[94]  David S Goodsell,et al.  Rapid Diversity‐Oriented Synthesis in Microtiter Plates for In Situ Screening of HIV Protease Inhibitors , 2003, Chembiochem : a European journal of chemical biology.

[95]  B. Frisch,et al.  Targeted liposomes: convenient coupling of ligands to preformed vesicles using "click chemistry". , 2006, Bioconjugate chemistry.

[96]  Zoran Radić,et al.  In situ selection of lead compounds by click chemistry: target-guided optimization of acetylcholinesterase inhibitors. , 2005, Journal of the American Chemical Society.

[97]  S. Hotha,et al.  "Click chemistry" inspired synthesis of pseudo-oligosaccharides and amino acid glycoconjugates. , 2006, The Journal of organic chemistry.

[98]  M. Finn,et al.  Head-to-tail peptide cyclodimerization by copper-catalyzed azide-alkyne cycloaddition. , 2005, Angewandte Chemie.

[99]  Ludger A. Wessjohann,et al.  What can a chemist learn from nature’s macrocycles? – A brief, conceptual view , 2005, Molecular Diversity.

[100]  Brendan L Wilkinson,et al.  A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing". , 2006, Journal of medicinal chemistry.

[101]  M. Congreve,et al.  Fragment-based lead discovery , 2004, Nature Reviews Drug Discovery.

[102]  M. G. Finn,et al.  Click Chemistry: Diverse Chemical Function from a Few Good Reactions. , 2001, Angewandte Chemie.

[103]  W. Dehaen,et al.  The application of "click chemistry" for the decoration of 2(1H)-pyrazinone scaffold: generation of templates. , 2005, Journal of combinatorial chemistry.

[104]  K. Jacobson,et al.  2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonists. , 2006, Journal of medicinal chemistry.

[105]  P. Wang,et al.  Syntheses and biological activity of bisdaunorubicins. , 2006, Bioorganic & medicinal chemistry.

[106]  N. F. Osborne,et al.  6-(substituted methylene)penems, potent broad spectrum inhibitors of bacterial beta-lactamase. IV. Kidney stability, serum binding and additional biological evaluation of racemic derivatives. , 1991, The Journal of antibiotics.

[107]  Jieping Zhu,et al.  Multicomponent Reactions: ZHU:MULTICOMPONENT REACTIONS O-BK , 2005 .

[108]  Mark L. Smythe,et al.  Exploring privileged structures: the combinatorial synthesis of cyclic peptides , 2002, J. Comput. Aided Mol. Des..

[109]  L. Capitán-Vallvey,et al.  Convenient methods for the synthesis of ferrocene-carbohydrate conjugates. , 2004, Organic letters.

[110]  A. Kros,et al.  The chemical modification of liposome surfaces via a copper-mediated [3 + 2] azide-alkyne cycloaddition monitored by a colorimetric assay. , 2006, Chemical communications.

[111]  G. Tron,et al.  One-pot synthesis of macrocycles by a tandem three-component reaction and intramolecular [3+2] cycloaddition. , 2006, Organic letters.

[112]  Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides. , 2005, Organic letters.

[113]  Z. Guan,et al.  A convergent synthesis of new β-turn mimics by click chemistry , 2006 .

[114]  Bradley D. Smith,et al.  Phosphatidylcholine-derived bolaamphiphiles via click chemistry. , 2007, Organic letters.

[115]  J. Thorson,et al.  Antibiotic optimization via in vitro glycorandomization , 2003, Nature Biotechnology.

[116]  Zoran Radić,et al.  Freeze-frame inhibitor captures acetylcholinesterase in a unique conformation. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[117]  David S Goodsell,et al.  1,2,3‐Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV‐1 Protease Inhibitors , 2005, Chembiochem : a European journal of chemical biology.

[118]  S. Chandrasekhar,et al.  Three-component coupling of alkynes, baylis-hillman adducts and sodium azide : a new synthesis of substituted triazoles , 2006 .