Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2009(11): 1865-1875
DOI: 10.1055/s-0029-1216802
DOI: 10.1055/s-0029-1216802
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Facile Synthesis of Fluorinated 1-Desazapurines
Further Information
Received
3 December 2008
Publication Date:
12 May 2009 (online)
Publication History
Publication Date:
12 May 2009 (online)
Abstract
A preparative approach towards 1-desazapurines, starting from 4(5)-aminoimidazoles and polyfluoroalkyl-containing 1,3-CCC-biselectrophiles was developed. As a result, a set of fluorinated 1-desazapurines was synthesized. Additionally, a synthetic route to 1-desazapurines bearing a sugar-mimicking group is proposed.
Key words
imidazoles - pyridines - annulations - fluorine - diketones - regioselectivity
-
1a
Dubey PK.Kumar RV.Naidu A.Kulkarni SMA. Asian J. Chem. 2002, 14: 1129 -
1b
Lee SCh,Choi JS,Oh JH,Park B,Kim YE,Lee JH,Shin D,Kim ChM,Hyun Y.-L,Lee ChS,Cho J.-M, andRo S. inventors; WO 83978 . ; Chem. Abstr. 2007, 147, 817587 -
1c
Kelly MG,Kincaid J,Duncton M,Sahasrabudhe K,Janagani S,Upasani RB,Wu G,Fang Y, andWei Zh.-L. inventors; US 194801 . ; Chem. Abstr. 2006, 145, 889269 -
1d
Randolph JT,Chen H,Degoey DA,Flentge ChA,Flosi WJ,Grampovnik DJ,Huang PP,Hutchinson DK,Kempf DJ,Klein LL, andYeung MC. inventors; US 159469 . ; Chem. Abstr. 2005, 143, 641882 -
1e
Kivlighn SD.Zingaro GJ.Gabel RA.Broten TP.Schorn TW.Schaffer LW.Naylor EM.Chakravarty PK.Patchett AA.Greenlee WJ.Siegl PKS. Am. J. Hypertens. 1995, 8: 58 -
2a
Pagani ED.Dundore RL.Bode DC.Bacon ER.Singh B.Lesher GY.Buchholz RA.Silver PJ. J. Cardiovasc. Pharmacol. 1994, 24: 403 -
2b
Joseph EC.Rees JA.Dayan A. Toxicol. Pathol. 1996, 24: 436 -
2c
Garvey DS,Saenz de Tejada I,Earl RA, andKhanapure SP. inventors; US 6331543. ; Chem. Abstr. 2001, 136, 916407 -
3a
Ida K,Otsubo N,Kuboyama T,Arai H,Watanabe A,Saki M,Hiura N,Manabe H,Takada H, andSaito J. inventors; WO 82905. ; Chem. Abstr. 2005, 143, 979654 -
3b
Magnuson S,Dixon J,Phillips B,Khire U,Wang L,Zhang Z,Patel M,Kumarasinghe E. S,Wickens P, andOblague A. inventors; WO 64932. ; Chem. Abstr. 2007, 147, 618350 -
3c
Bavetsias V.Sun C.Bouloc N.Reynisson J.Workman P.Linardopoulos S.McDonald E. Bioorg. Med. Chem. Lett. 2007, 17: 6567 -
4a
Hackova D.Hocek M.Dvorakova H.Votruba I. Tetrahedron 1999, 55: 11109 -
4b
Koch M,Den H,Jacobus A,Koomen J,Wanner G.-J,Martinus J, andRoelof FW. inventors; WO 27365. -
4c
Erion MDM.Reddy R. J. Am. Chem. Soc. 1998, 120: 3295 -
4d
Veliz EA.Stephens OM.Beal PA. Org. Lett. 2001, 3: 2969 - For ‘de novo’ synthesis, see, for example:
-
5a
Rolfes RJ. Biochem. Soc. Trans. 2006, 34: 786 -
5b
Christopherson RJ.Lyons SD.Wilson PK. Acc. Chem. Res. 2002, 35: 961 -
5c
Zalkin H.Dixon JE. Prog. Nucleic Acid Res. Mol. Biol. 1992, 42: 259 - For ‘salvage’ synthesis, see, for example:
-
6a
Manfredi JP.Holmes EW. Annu. Rev. Physiol. 1985, 47: 691 -
6b
Berens RL.Krug EC.Marr JJ. Biochem. Mol. Biol. Parasites 1995, 89 -
7a
Lawhorn BG.Mehl RA.Begley TP. Org. Biomol. Chem. 2004, 2: 2538 ; and references cited therein -
7b
Humpfries MJ.Ramsden CA. Synlett 1995, 203 -
7c
Vyskocilova P.Hornik P.Friedecky D.Frycak P.Lemr K.Adam T. Nucleosides, Nucleotides Nucleic Acids 2006, 25: 9 -
8a
Al-Shaar AH.Gilmour DW.Lythgoe DJ.McClenaghan I.Ramsden Ch. J. Chem. Soc., Chem. Commun. 1989, 551 -
8b
Clayton R.Davis ML.Fraser W.Li W.Ramsden ChA. Synlett 2002, 1483 -
8c
Wang Z.Huynh HK.Han B.Krishnamurthy R.Eschenmoser A. Org. Lett. 2003, 5: 2067 -
8d
Al-Shaar AHM.Gilmour DW.Lythgoe DJ.McClenaghan I.Ramsden ChA. J. Chem. Soc., Perkin Trans. 1 1992, 2779 -
8e
Al-Shaar Adnan HM.Chambers RK.Gilmour DW.Lythgoe DJ.McClenaghan I.Ramsden ChA. J. Chem. Soc., Perkin Trans. 1 1992, 2789 -
8f
Iaroshenko VO.Volochnyuk DM.Wang Y.Vovk MV.Boiko VJ.Rusanov EB.Groth UM.Tolmachev AO. Synthesis 2007, 3309 -
9a
Iaroshenko VO.Volochnyuk DM.Wang Y.Vovk MV.Boiko VJ.Rusanov EB.Groth UM.Tolmachev AO. Synthesis 2007, 3309 -
9b
Iaroshenko VO.Groth U.Kryvokhyzha NV.Obeid S.Tolmachev AA.Wesch T. Synlett 2008, 343 -
9c
Volochnyuk DM.Pushechnikov AO.Krotko DG.Sibgatulin DA.Kovalyova SA.Tolmachev AA. Synthesis 2003, 1531 -
9d
Vovk MV.Bolbut AV.Boiko VI.Pirozhenko VV.Chernega AN.Tolmachev AA. Chem. Heterocycl. Compd. (N. Y., NY,
U. S.) 2004, 40: 370 -
9e
Vovk MV.Bol’but AV.Dorokhov VI.Pyrozhenko VV. Synth. Commun. 2002, 32: 3749 -
9f
Iaroshenko VO.Volochnyuk DM.Kryvokhyzha NV.Martyloga A.Sevenard DV.Groth U.Brand J.Chernega AN.Shivanyuk AN.Tolmachev AA. Synthesis 2008, 2337 -
9g
Iaroshenko VO.Sevenard DV.Kotljarov AV.Volochnyuk DM.Tolmachev AO.Sosnovskikh VYa. Synthesis 2008, 731 -
10a
Lythgoe DJ.Ramsden CA. Adv. Heterocycl. Chem. 1994, 61: 1 -
10b
Groziak MP.Ding H. Acta Chim. Slov. 2000, 47: 1 -
11a
Kinoshita T.Watanabe H.Sato S.Tamura C. Bull. Chem. Soc. Jpn. 1980, 53: 442 -
11b
Hosmane RS.Burnett FN.Albert MS. J. Org. Chem. 1984, 49: 1212 -
11c
Naylor RN.Shaw G.Wilson DV.Butler DN. J. Chem. Soc. 1961, 4845 - 12
Lissel M. Liebigs Ann. Chem. 1987, 77 - 13
D’Aurio M.D’Onofrio F.Suwinski J.Swierczek K. Tetrahedron 1993, 49: 3899 -
14a
Beauchamp LM.Serling BL.Kelsey JE.Biron KK.Collins P.Selway J.Lin JC.Schaeffer HJ. J. Med. Chem. 1988, 31: 144 -
14b
Kumar R.Semaine W.Johar M.Tyrrell DLJ.Agrawal B. J. Med. Chem. 2006, 49: 3693 - 15
Yang M.Ye W.Schneller SW. J. Org. Chem. 2004, 69: 3993 - 16
Hodgson DM.Witherington J.Moloney BA. J. Chem. Soc., Perkin Trans. 1 1994, 3373 - 17
Ichiro H.Tsuneo M.Michiko K.Shigeyuki Y. J. Am. Chem. Soc. 2007, 129: 15549 -
18a
Luscombe C.Pedersen J.Uren E.Locarnini S. J. Hepatol. 1996, 24: 766 -
18b
Kruining J.Heijtink RA.Schalm SW. J. Hepatol. 1995, 22: 263 -
19a
Husaka T.Yamamoto H.Shibata M.Muroi M.Kishi T.Mizuno K. J. Antibiot. 1967, 21: 255 -
19b
Kishi T.Muroi M.Kusaka T.Nishikawa M.Kamiya K.Mizuno K. Chem. Pharm. Bull. 1972, 20: 940 -
19c
Crimmins MT. Tetrahedron 1998, 54: 9229 - 20
Vince R.Hua M. J. Med. Chem. 1990, 33: 17 -
21a
Reid JC.Calvin M. J. Am. Chem. Soc. 1950, 72: 2948 -
21b
Park JD.Brown HA.Lacher JR. J. Am. Chem. Soc. 1953, 75: 4753 -
21c
Pashkevich KI.Khomutov OG.Sevenard DV. Russ. J. Org. Chem. 1998, 34: 1727 ; Zh. Org. Khim. 1998, 34, 1798 -
21d
Sevenard DV.Lork E. J. Fluorine Chem. 2004, 125: 125 -
21e
Sevenard, D. V.; Sosnovskikh, V. Ya.; Iaroshenko, V. O. unpublished results.
-
22a
Malliet P,Le Brun A,Thompson F, andTiraboschi G. inventors; WO 108685. -
22b
Decreau RA.Collman JP.Yang Y.Yan Y.Devarai NK. J. Org. Chem. 2007, 72: 2794