Continuous Flow Hydrogenation of Functionalized Pyridines

The heterogeneous hydrogenation of substituted pyridines has been accomplished by employing a continuous flow hydrogenation device that incorporates in situ hydrogen generation by electrolysis of H2O and pre-packed catalyst cartridges. In general, the hydrogenation reactions proceeded smoothly regardless of the supported precious metal catalyst (Pd/C, Pt/C, or Rh/C). By using 30–80 bar of hydrogen pressure at 60–80 °C full conversion was typically achieved in all cases at a flow rate of 0.5 mL min–1, providing the corresponding piperidines in high yields. For disubstituted pyridines, variations in stereoselectivity were observed depending on both the metal catalyst and the temperature/pressure of the hydrogenation reaction. For ethyl nicotinate the selectivity between partial and full hydrogenation could be tuned depending on the hydrogen pressure, solvent, and the choice of supported metal catalyst. Changing the hydrogen source from H2O to D2O allowed the preparation of deuteriated derivatives. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

[1]  C. Kappe,et al.  Controlled microwave heating in modern organic synthesis. , 2004, Angewandte Chemie.

[2]  F. Fülöp,et al.  New data to the origin of rate enhancement on the Pt-cinchona catalyzed enantioselective hydrogenation of activated ketones using continuous-flow fixed-bed reactor system , 2008 .

[3]  F. Fülöp,et al.  Continuous enantioselective hydrogenation of activated ketones on a pt-cd chiral catalyst: use of h-cube reactor system , 2006 .

[4]  M. Freifelder Hydrogenation of Pyridinecarboxylic Acids with Platinum Catalyst , 1962 .

[5]  C. Oliver Kappe,et al.  Practical microwave synthesis for organic chemists , 2008 .

[6]  C. Larpent,et al.  Mechanistic aspects of alkenes hydrogenation and deuteration catalyzed by dispersion of hydroxyhydridorhodium colloids in aqueous medium , 1990 .

[7]  Steven V. Ley,et al.  Optimisation of Conditions for O‐Benzyl and N‐Benzyloxycarbonyl Protecting Group Removal using an Automated Flow Hydrogenator , 2007 .

[8]  Steven V Ley,et al.  The use of a continuous flow-reactor employing a mixed hydrogen-liquid flow stream for the efficient reduction of imines to amines. , 2005, Chemical communications.

[9]  R. Chěnevert,et al.  Enzymatic Route to Chiral, Nonracemic cis-2,6- and cis,cis-2,4,6-Substituted Piperidines. Synthesis of (+)-Dihydropinidine and Dendrobate Alkaloid (+)-241D , 1996 .

[10]  T. Donohoe,et al.  PROSPECTS FOR STEREOCONTROL IN THE REDUCTION OF AROMATIC COMPOUNDS , 1996 .

[11]  L. D. Quin,et al.  1,4,5,6-Tetrahydropyridines from Catalytic Reduction of Nicotinoyl Derivatives and Their Ring Opening with Hydrazine , 1966 .

[12]  J. Concellón,et al.  Highly Selective Reaction of α-Halo-α,β-unsaturated Esters with Ketones or Aldehydes Promoted by SmI2: An Efficient Alternative Access to Baylis−Hillman Adducts , 2005 .

[13]  M. Freifelder Hydrogenation of Pyridines and Quinolines , 1963 .

[14]  G. Ertl,et al.  Handbook of Heterogeneous Catalysis , 1997 .

[15]  W. Houlihan,et al.  Synthesis and antiinflammatory acitivity of 2-aryl-2-alpha-piperidyl-1,3-dioxanes. , 1969, Journal of medicinal chemistry.

[16]  D. Vos,et al.  Microwave-promoted racemization and dynamic kinetic resolution of chiral amines over Pd on alkaline earth supports and lipases , 2008 .

[17]  J. Kremsner,et al.  Investigating the existence of nonthermal/specific microwave effects using silicon carbide heating elements as power modulators. , 2008, The Journal of organic chemistry.

[18]  J. Daly,et al.  Alkaloids from amphibian skin: a tabulation of over eight-hundred compounds. , 2005, Journal of natural products.

[19]  Ferenc Darvas,et al.  Continuous-flow high pressure hydrogenation reactor for optimization and high-throughput synthesis. , 2006, Journal of combinatorial chemistry.

[20]  Michael B. Smith,et al.  Cis-3,5-dimethyl-3,5-piperidinedicarboxylic acid, an amino diacid variant of Kemp's triacid , 1994 .

[21]  V. Háda,et al.  Diastereoselective heterogeneous catalytic hydrogenation of N-heterocycles. Part I. Hydrogenation of pyridines , 2000 .

[22]  E. Kornfeld,et al.  Conidine—Synthesis, Polymerization and Derivatives , 1960 .

[23]  S. Chandrasekhar,et al.  A novel one-pot conversion of amines to homologated esters in poly(ethylene glycol) ☆ , 2007 .

[24]  P. Ornstein,et al.  An improved synthesis of homoproline and derivatives , 1990 .

[25]  M. Freifelder,et al.  Reductions with Ruthenium. II. Its Use in the Hydrogenation of Pyridines1 , 1961 .

[26]  F. Fülöp,et al.  New Data on the Orito Reaction: Effect of Substrate Structure on Nonlinear Phenomenon , 2008 .

[27]  Araceli G. Campaña,et al.  Unprecedented hydrogen transfer from water to alkenes and alkynes mediated by TiIII and late transition metals. , 2007, Organic letters.

[28]  D. Murzin,et al.  Ethyl pyruvate hydrogenation under microwave irradiation , 2007 .

[29]  R. Lyle,et al.  METHYL 1-METHYL-1,2,3,6-TETRAHYDROISONICOTINATE , 1955 .

[30]  M. Moriguchi,et al.  An efficient access to both enantiomers of pipecolic acid , 2005 .

[31]  D. Mingos,et al.  Arcing and other microwave characteristics of metal powders in liquid systems , 2000 .

[32]  D. Knight,et al.  Biocides under REACH , 2007 .

[33]  J Jan Meuldijk,et al.  Vanishing microwave effects : Influence of heterogeneity , 2007 .

[34]  F. Fülöp,et al.  Enantioselective hydrogenation of α,β-unsaturated carboxylic acids in fixed-bed reactor , 2007 .

[35]  A. Potthast,et al.  A general, selective, high-yield N-demethylation procedure for tertiary amines by solid reagents in a convenient column chromatography-like setup. , 2004, Organic letters.

[36]  G. N. Walker Vinylogous Amides of 2-Methylaminoethanol and Their Behavior with Lithium Aluminum Hydride. Vinylogous Urethanes of Ethanolamines and Their Acetylation , 1962 .

[37]  Ferenc Darvas,et al.  A Novel Method for High-Throughput Reduction of Compounds through Automated Sequential Injection into a Continuous-Flow Microfluidic Reactor , 2005 .

[38]  G. Vanier Simple and Efficient Microwave-Assisted Hydrogenation Reactions at ­Moderate Temperature and Pressure , 2007 .

[39]  C. Kappe,et al.  Heterogeneous hydrogenation reactions using a continuous flow high pressure device. , 2005, Journal of combinatorial chemistry.

[40]  R. Varma,et al.  Hydrodechlorination of chlorinated benzenes in a continuous microwave reactor , 2004 .

[41]  H. Blaser,et al.  Enantioselective synthesis of ethyl nipecotinate using cinchona modified heterogeneous catalysts , 1999 .

[42]  R. Adams,et al.  REDUCTION OF PYRIDINE HYDROCHLORIDE AND PYRIDONIUM SALTS BY MEANS OF HYDROGEN AND PLATINUM-OXIDE PLATINUM BLACK. XVIII1 , 1928 .

[43]  M. Freifelder,et al.  Hydrogenation of Substituted Pyridines with Rhodium on Carbon Catalyst1 , 1962 .

[44]  U. Holzgrabe,et al.  Microwave-enhanced hydrogenations at medium pressure using a newly constructed reactor , 2005 .

[45]  Christian C. Gruber,et al.  An algorithm for the deconvolution of mass spectroscopic patterns in isotope labeling studies. Evaluation for the hydrogen-deuterium exchange reaction in ketones. , 2007, The Journal of organic chemistry.

[46]  I. Horibe,et al.  Selective reduction of aryl halides and α,β-unsaturated esters with sodium borohydride-cuprous chloride in methanol and its application to deuterium labeling , 1989 .

[47]  J. Kane,et al.  Recent Advances in the Synthesis of Piperidones and Piperidines , 2003 .

[48]  Mao Chen,et al.  Asymmetric Hydrogenation of Pyridines: Enantioselective Synthesis of Nipecotic Acid Derivatives , 2006 .

[49]  Jeffrey Y. Pan,et al.  Construction and validation of an automated flow hydrogenation instrument for application in high-throughput organic chemistry. , 2008, Journal of combinatorial chemistry.

[50]  C. Kappe,et al.  Microwave-assisted solution phase synthesis of dihydropyrimidine C5 amides and esters , 2006 .

[51]  S. Schaus,et al.  Asymmetric Mannich reaction of dicarbonyl compounds with alpha-amido sulfones catalyzed by cinchona alkaloids and synthesis of chiral dihydropyrimidones. , 2007, The Journal of organic chemistry.

[52]  F. Glorius Asymmetric hydrogenation of aromatic compounds. , 2005, Organic & biomolecular chemistry.

[53]  G. Fodor,et al.  Diastereoisomeric 2-aryl-6-methyl-3,4 (1,2-piperido)-oxazines , 1968 .