2-Hydroxy-6-(Trifluoromethyl) Pyridine - Globy

18 Aug.,2025

 

2-Hydroxy-6-(Trifluoromethyl) Pyridine - Globy

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Thieme E-Journals - Synthesis / Full Text

Synthesis (7): -  
DOI: 10./s-- PAPER© Georg Thieme Verlag Stuttgart ˙ New York

Catalytic Hydrogenation of 3-Amino-6-(trifluoromethyl)-5,6-dihydropyridin-2(1H)-ones and Its Use in the Synthesis of Trifluoromethyl-Containing Mimetics of Ornithine and Thalidomide

Nataliya A. Tolmachovaa, Violetta G. Dolovanyuka, Igor I. Gerusa, Ivan S. Kondratova, Vitaliy V. Polovinkob, Klaus Berganderc, Günter Haufe*c
a Institute of Bioorganic Chemistry and Petrochemistry, National Ukrainian Academy of Science, Murmanska 1, Kiev 94 , Ukraine
b Enamine Ltd., Alexandra Matrosova str. 23, Kiev, Ukraine
c Organisch-Chemisches Institut der Universität Münster, Corrensstraße 40, Münster, Germany
Fax: +49(251); : ;
Further Information

Publication History

Received 8 December
Publication Date:
01 March (online)
  • Abstract
  • Full Text
  • References
  • Supplementary Material

Abstract

A series of 3-amino-6-(trifluoromethyl)-5,6-dihydropyridin-2(1H)-ones and 6-hydroxy-5,6-dihydropyridin-2(1H)-ones were hydrogenated to give the corresponding piperidinones. These lactams were used for the synthesis of novel trifluoromethyl-containing ornithine analogues and thalidomide mimetics.

Key words

amino acids - catalysis - halides - heterocycles - hydrogenation - piperidinones

    References

  • For some recent examples, see:
  • 1a Boeglin D. Hamdan FF. Melendez RE. Cluzeau J. Laperriere A. Héroux M. Bouvier M. Lubell WD. J. Med. Chem.  ,  50:   
  • 1b Manzoni L. Bassanini M. Belvisi L. Motto I. Scolastico C. Castorina M. Pisano C. Eur. J. Org. Chem.  ,   
  • 1c Smallheer JM. Wang S. Laws ML. Nakajima S. Hu Z. Han W. Jacobson I. Luettgen JM. Rossi KA. Rendina AR. Knabb RM. Wexler RR. Lam PYS. Quan ML. Bioorg. Med. Chem. Lett.  ,  18:   
  • 1d Mezo AR. McDonnell KA. Castro A. Fraley C. Bioorg. Med. Chem.  ,  16:   
  • 1e Lewis JA. Daniels RN. Lindsley CW. Org. Lett.  ,  10:   
  • 2a Kirsch P. Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications   Wiley-VCH; Weinheim: . 
  • 2b Uneyama K. Organofluorine Chemistry   Blackwell; Oxford: . 
  • 3a Bégué J.-P. Bonnet-Delpon D. Bioorganic and Medicinal Chemistry of Fluorine   John Wiley; Hoboken: .  p.365 
  • 3b Fluorine in Medicinal Chemistry and Chemical Biology   Ojima I. Wiley; Chichester: . 
  • 3c Fluorinated Heterocyclic Compounds: Synthesis, Chemistry, and Applications   Petrov VA. John Wiley; Hoboken: .  p.399-507  
  • 3d Theodoridis G. Adv. Fluorine Sci.  ,  2:  121 
  • 4 Nishimura S. Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis   Wiley-Interscience; New York: .  p.511-513  
  • For some recent examples, see:
  • 5a Shi G.-F. Li J.-Q. Jiang X.-P. Cheng Y. Tetrahedron  ,  64:   
  • 5b Jiang X.-P. Cheng Y. Shi G.-F. Kang Z.-M. J. Org. Chem.  ,  72:   
  • 5c Padwa A. Heidelbaugh TM. Kuethe JT. J. Org. Chem.  ,  65:   
  • For some recent examples, see:
  • 6a Liang G.-B. Qian X. Biftu T. Singh S. Gao Y.-D. Scapin G. Patel S. Leiting B. Patel R. Wu J. Zhang X. Thornberry NA. Weber AE. Bioorg. Med. Chem. Lett.  ,  18:   
  • 6b McCarthy AR. Hartmann RW. Abell AD. Bioorg. Med. Chem. Lett.  ,  17:   
  • 6c Guthikonda RN. Shah SK. Pacholok SG. Humes JL. Mumford RA. Grant SK. Chabin RM. Green BG. Tsou N. Ball R. Fletcher DS. Luell S. MacIntyre DE. MacCoss M. Bioorg. Med. Chem. Lett.  ,  15:   
  • 6d Fischer C, Munoz B, Zultanski S, Methot J, Zhou H, and Brown WC. inventors; WO  .  ; Chem Abstr. , 150,
  • 7 Tolmacheva NA. Gerus II. Dolovanyuk VG. Kondratov IS. Haufe G. Eur. J. Org. Chem.  ,   
  • 8 Gerus II. Tolmachova NA. Vdovenko SI. Fröhlich R. Haufe G. Synthesis  ,   
  • 10a Molteni M. Pesenti C. Sani M. Volonterio A. Zanda M. J. Fluorine Chem.  ,  125:   
  • 10b Bigotti S. Meille SV. Volonterio A. Zanda M. J. Fluorine Chem.  ,  129:  767 
  • 10c Molteni M. Bellucci MC. Bigotti S. Mazzini S. Volonterio A. Zanda M. Org. Biomol. Chem.  ,  7:   
  • 10d Black WC. Bayly CI. Davis DE. Desmarais S. Falgueyret J.-P. Leger S. Li CS. Masse F. McKay DJ. Palmer JT. Percival MD. Robichaud J. Tsoub N. Zambonia R. Bioorg. Med. Chem. Lett.  ,  15:   
  • 10e Li CS. Deschenes D. Desmarais S. Falgueyret J.-P. Gauthier JY. Kimmel DB. Leger S. Masse F. McGrath ME. McKay DJ. Percival MD. Riendeau D. Rodan SB. Therien M. Truong VL. Weslowski G. Zamboni R. Black WC. Bioorg. Med. Chem. Lett.  ,  16:   
  • For recent reviews, see
  • 11a Melchert M. List A. Int. J. Biochem. Cell Biol.  ,  39:   
  • 11b Huang Y.-T. Hsu CW. Chiu TH. Tzu Chi Med. J.  ,  20:  188 
  • 12 Weiss J. Weiss T. Handbook of Ion Chromatography   3rd ed.:  Wiley-VCH; Weinheim: . 
9

Crystallographic data for compounds cis-10a and cis-2a have been deposited with the Cambridge Crystallographic Data Centre as supplementary publications CCDC and CCDC , respectively; copies can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44() or : ].

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  • Supplementary Material