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DOI: 10.1055/s-2006-942446
Synthesis of 2-(Arylsulfonyl)-4-hydroxypyridines by Hetero-Diels-Alder Reaction of 1,3-Bis-Silyl Enol Ethers with Arylsulfonyl Cyanides
Publication History
Publication Date:
28 June 2006 (online)
Abstract
2-(Arylsulfonyl)-4-hydroxypyridines were prepared by Hetero-Diels-Alder reaction of 1,3-bis(trimethylsiloxy)buta-1,3-dienes (1,3-bis-silyl enol ethers) with arylsulfonyl cyanides. The products were transformed into 4-aryl-2-(arylsulfonyl)pyridines by Suzuki cross-coupling reactions of the corresponding enol triflates.
Key words
1,3-bis-silyl enol ethers - hetero-Diels-Alder - arylsulfonyl cyanide - pyridine
-
1a
Boger DL.Weinreb SM. Hetero-Diels-Alder Methodology in Organic Synthesis Academic Press; San Diego CA: 1987. -
1b
Tietze LF.Schneider C. J. Org. Chem. 1991, 56: 2476 - 2 For cycloaddition reactions of nitriles, see:
Collier S.Langer P. In Science of SynthesisShinkai I.Murahashi S. Thieme; Stuttgart: 2004. Chap. 19.5.15. - 3
Breitmaier E.Rüffer U. Synthesis 1989, 623 - Sulfonyl cyanides have been used as electrophilic cyanation reagents, see:
-
4a
Christophersen C.Begrup M.Ebdrup S.Petersen H.Vedsoe P. J. Org. Chem. 2003, 68: 9513 -
4b
Boymond L.Rottlaender M.Cahiez G.Knochel P. Angew. Chem. Int. Ed. 1998, 37: 1701 -
4c
Jensen T.Teiler J.Waernmark K. J. Org. Chem. 2002, 67: 6008 - 5
Wang T.Hendrickson J. Org. Prep. Proced. Int. 2003, 35: 623 - 6
van Leusen AM.Jagt JC. , - 7
McClure CK.Link JS. J. Org. Chem. 2003, 68: 8256 - 8 For a review of 1,3-bis-silyl enol ethers, see:
Langer P. Synthesis 2002, 441 -
9a
Hirokawa Y.Horikawa T.Kato S. Chem. Pharm. Bull. 2000, 48: 1847 -
9b
Cutshall NS.Ursino R.Kucera KA.Latham J.Ihle NC. Bioorg. Med. Chem. Lett. 2001, 14: 1951 -
9c
Bonnet V.Mongin F.Trecourt F.Queguiner G.Knochel P. Tetrahedron 2002, 58: 4429 -
9d
Ohnmacht CJ.Russell K.Empfield JR.Frank CA.Gibson KH. J. Med. Chem. 1996, 39: 4592 -
9e
Yogi S.Hokama K.Tsuge O. Bull. Chem. Soc. Jpn. 1987, 60: 335 -
9f
Reiffenrath V.Bremer M. Angew. Chem., Int. Ed. Engl. 1994, 33: 1386 ; Angew. Chem. 1994, 106, 1435 -
9g
Furukawa N.Tsuruoka M.Fujihara H. Heterocycles 1986, 24: 3337 - 10
Molander GA.Cameron KO. J. Am. Chem. Soc. 1993, 115: 830 - 11
Anderson G.Cameron DW.Feutrill GI.Read RW. Tetrahedron Lett. 1981, 22: 4347
References
Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-295095(3c) and CCDC-297417(3e). Copies of this data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033 or e-mail: deposit@ccdc.cam.ac.uk) or via www.ccdc.cam.ac.uk/conts/retrieving.html.