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 YorkCatalytic 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
Supporting Information for this article is available online:
- Supporting Information
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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