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DOI: 10.1055/s-2002-35978
Synthesis of the Precursor of Anti-Inflammatory Agents by Cross-Coupling Using Electrogenerated Highly Reactive Zinc
Publication History
Publication Date:
06 December 2002 (online)
Abstract
Highly reactive zinc metal was readily prepared by electrolysis of a DMF solution containing naphthalene and a supporting electrolyte in a one-compartment cell fitted with a platinum cathode and a zinc anode. This reactive zinc was used for efficient transformation of ethyl 2-bromoacrylate into the corresponding organozinc compound, which was reacted with various aryl iodides in the presence of palladium catalyst to give the corresponding cross-coupling products, ethyl 2-arylpropenoates, in high yields. These cross-coupling reactions were successfully applied to a synthesis of the precursors of non-steroidal anti-inflammatory agents such as ibuprofen, naproxen, ketoprofen, loxoprofen, indoprofen, suprofen, cicloprofen, and flurbiprofen.
Key words
anti-inflammatory agents - cross-coupling - reactive zinc - organometallic reagents - electrolysis
- 1
Rieu JP.Boucherle A.Cousse H.Mouzin G. Tetrahedron 1986, 42: 4095 -
2a
Kenyon WG.Kaiser EM.Hauser ChR. J. Org. Chem. 1965, 30: 2937 -
2b
Hicks TA.Smith CE.Williamson WRN.Day EH. J. Med. Chem. 1979, 22: 1460 -
2c
Harrison IT.Lewis B.Nelson P.Rooks W.Roszkiwski A.Tomolonis A.Fried JH. J. Med. Chem. 1969, 13: 203 -
2d
Closse A.Haefliger W.Hauser D.Gubler HU.Dewald B.Baggiolini M. J. Med. Chem. 1981, 24: 1465 -
2e
Tamura Y.Yoshimoto Y.Kunimoto K.Tada S.Matsumura S.Maruyama M.Shibata Y.Enomoto H. J. Med. Chem. 1981, 24: 43 -
2f
Fadel A. Synlett 1992, 48 -
3a
Kobler H.Schuster KM.Simchen G. Liebigs Ann. Chem. 1978, 1946 -
3b
Foulkes JA.Hutton J. Synth. Commun. 1979, 9: 625 -
3c
Bakshi SP.Turner EE. J. Chem. Soc. 1961, 171 -
4a
Lawrence NJ.Liddle J.Bushell SM.Jackson DA. J. Org. Chem. 2002, 67: 457 -
4b
Arai A.Ohara Y.Lizumi T.Takakuwa Y. Tetrahedron Lett. 1983, 24: 1531 -
4c
Pinhey JT.Rowe BA. Tetrahedron Lett. 1980, 21: 965 -
4d
Sprague PW.Heikes JE. J. Med. Chem. 1977, 20: 726 -
4e
Hino K.Nakamura H.Nagai Y.Uno H.Nishimura H. J. Med. Chem. 1983, 26: 222 -
5a
Higgins SD.Thomas CB. J. Chem. Soc., Perkin Trans. 1 1982, 235 -
5b
Fujii K.Nakao K.Yamauchi T. Synthesis 1982, 456 -
5c
Tamura Y.Shirouchi Y.Haruta JI. Synthesis 1984, 231 -
5d
Fujii K.Nakao K.Yamauchi T. Synthesis 1983, 444 -
5e
Giordano C.Castaldi G.Casagrande F.Belli A. J. Chem. Soc., Perkin Trans. 1 1982, 2575 -
5f
Castaldi G.Belli A.Uggeri F.Giordano C. J. Org. Chem. 1983, 48: 4658 -
5g
Goosen A.Cleland CW. J. Chem. Soc., Chem. Commun. 1982, 1311 -
5h
Tsuchihashi G.Mitamura S.Kitajima K.Kobayashi K. Tetrahedron Lett. 1982, 23: 5427 -
5i
Shioiri T.Kawai N. J. Org. Chem. 1978, 43: 2936 -
6a
Hamon DPG.M-Westropp RA.Newton JL. Tetrahedron Lett. 1993, 34: 5333 -
6b
Hamon DPG.M-Westropp RA.Newton JL. Tetrahedron: Asymmetry 1993, 4: 1435 -
7a
Ohta T.Takaya H.Kitamura M.Nagai K.Noyori R. J. Org. Chem. 1987, 52: 3176 -
7b
Ashby MT.Halpern J. J. Am. Chem. Soc. 1991, 113: 589 -
7c
Manimaran T.Wu T.-C.Klobucar WD.Kolich CH.Stahly GP. Organometallics 1993, 12: 1467 -
7d
Zhang X.Uemura T.Matsumura K.Sayo N.Kumobayashi H.Takaya H. Synlett 1994, 501 -
7e
Mashima K.Kusano K.Sato N.Matsumura Y.Nozaki K.Kumobayashi H.Sayo N.Hori Y.Ishizaki T.Akutagawa S.Takaya H. J. Org. Chem. 1994, 59: 3064 - 8
Kamekawa H.Senboku H.Tokuda M. Electrochimica Acta 1997, 42: 2117 - 9
Aishah AJ.Kurono N.Tokuda M. Synlett 2001, 1944 - 10
Aishah AJ.Kurono N.Tokuda M. Tetrahedron 2002, 58: 7477 - 11
Levin JI. Tetrahedron Lett. 1993, 34: 6211 - 12
Tokuda M.Mimura N.Karasawa T.Fujita H.Suginome H. Tetrahedron Lett. 1993, 47: 7607 - 13 Tokuda M., Kurono N., Mimura N.; Chem. Lett.; 1996, 1091
- 14
Tokuda M. Novel Trends in Electroorganic SynthesisTorii S. Kodansha Ltd.; Tokyo: 1995. p.241 - 15
Kurono N.Sugita K.Takasugi S.Tokuda M. Tetrahedron 1999, 55: 6097 - 16
Rachon J.Goedken V.Walborsky HM. J. Org. Chem. 1989, 54: 1006 - 17
Barluenga J.Campos PJ.Gonzalez JM.Asensio G. J. Chem. Soc., Perkin Trans. 1 1984, 2623 - 18 2-(4-Bromobenzoyl)thiophene was
prepared according to the reported procedure:
McKean DR.Parrinello G.Renaldo AF.Stille JK. J. Org. Chem. 1987, 52: 422 -
19a
Bando T.Namba Y.Shishido K. Tetrahedron: Asymmetry 1997, 8: 2159 -
19b
DMF was used instead of HMPA
-
20a
Wagner PJ.Waite CI. J. Phys. Chem. 1995, 99: 7388 -
20b
Ebert GW.Klein WR. J. Org. Chem. 1991, 56: 4744 - 21
Minabe M.Suzuki K. Bull. Chem. Soc. Jpn. 1972, 45: 3196 - 22
Cho WS.Kim HJ.Littler BJ.Millar MA.Lee CH.Lindsey JSJ. J. Org. Chem. 1999, 64: 7890