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DOI: 10.1055/s-0030-1258478
Synthesis of 3-Alkyl-4-(chloromethyl)-1-RSO2-1H-pyrrol-2(5H)-ones, Using a Sequential ATRC/[1,2]-Elimination, from 2,2-Dichloro-N-(2-chloroallyl)-N-RSO2-amides
Publikationsverlauf
Publikationsdatum:
16. März 2011 (online)

Abstract
The preparation of 3-alkyl-4-(chloromethyl)-1-RSO2-1H-pyrrol-2(5H)-ones was efficiently accomplished through a [1,2]-elimination of γ-lactams derived from the copper(I)-catalysed ATRC of 2,2-dichloro-N-(2-chloroallyl)-N-RSO2-amides. The two reactions can be integrated into a sequential one-pot process.
Key words
copper - cyclization - elimination - lactams - radical reaction
- 1a
Rowlands GJ. Tetrahedron 2010, 66: 1593 - 1b
Eckenhoff WT.Pintauer T. Catal. Rev. 2010, 52: 1 - 1c
Clark AJ. Chem. Soc. Rev. 2002, 31: 1 - 1d
Kobrakov KI.Ivanov AV. Chem. Heterocycl. Compd. (Engl. Transl.) 2001, 37: 529 - 1e
Ram RN.Kumar N.Singh N. J. Org. Chem. 2010, 75: 7408 - 1f
Udding JH.Tuijp KCJM.van Zandem MNA.Hiemstra H.Speckamp WN. J. Org. Chem. 1994, 59: 1993 - 1g
Alcaide B.Almendros P.Luna A. Chem. Rev. 2009, 109: 3817 - 1h
Severin K. Curr. Org. Chem. 2006, 10: 217 - 1i
Nagashima H.Itoh K. J. Synth. Org. Chem., Jpn. 1995, 53: 298 - 2a
Pattarozzi M.Roncaglia F.Giangiordano V.Davoli P.Prati F.Ghelfi F. Synthesis 2010, 694 - 2b
Rowlands GJ. Tetrahedron 2009, 65: 8603 - 3a
Motoyama Y.Kamo K.Yuasa A.Nagashima H. Chem. Commun. 2010, 46: 2256 - 3b
McGonacle FI.Brown L.Cooke A.Sutherland A. Org. Biomol. Chem. 2010, 8: 3418 - 3c
Clark AJ.Wilson P. Tetrahedron Lett. 2008, 49: 4848 - 3d
Bull JA.Hutchings MG.Luján C.Quayle P. Tetrahedron Lett. 2008, 49: 1356 - 3e
Thommes K.Içli B.Scopelliti R.Severin K. Chem. Eur. J. 2007, 13: 6899 - 3f
Clark AJ.Geden JV.Thom S. J. Org. Chem. 2006, 71: 1471 - 4a
Ghelfi F.Pattarozzi M.Roncaglia F.Giangiordano V.Parsons AF. Synth. Commun. 2010, 40: 1040 - 4b
Bellesia F.Danieli C.De Buyck L.Galeazzi R.Ghelfi F.Mucci A.Orena M.Pagnoni UM.Parsons AF.Roncaglia F. Tetrahedron 2006, 62: 746 - 4c
De Buyck L.Cagnoli R.Ghelfi F.Merighi G.Mucci A.Pagnoni UM.Parsons AF. Synthesis 2004, 1680 - 4d
De Buyck L.Danieli C.Ghelfi F.Pagnoni UM.Parsons AF.Pattarozzi M.Roncaglia F. Tetrahedron 2005, 61: 2871 - 4e
Roncaglia F.Stevens CV.Ghelfi F.Van der Steen M.Pattarozzi M.De Buyck L. Tetrahedron 2009, 65: 1481 - 4f
Cagnoli R.Ghelfi F.Pagnoni UM.Parsons AF.Schenetti L. Tetrahedron 2003, 59: 9951 - 4g
Bryans JS.Chessum NEA.Huther N.Parsons AF.Ghelfi F. Tetrahedron 2003, 59: 6221 - 4h
Ghelfi F.Bellesia F.Forti L.Ghirardini G.Grandi R.Libertini E.Montemaggi MC.Pagnoni UM.Pinetti A.De Buyck L.Parsons AF. Tetrahedron 1999, 55: 5839 - 4i
Masahiko I.Masahiko S.Hitoshi N.Hiroshi K.Hiroshi Y. Pest Manag. Sci. 2004, 60: 981 - 4j
Ishibashi H.Uemura N.Nakatani H.Okazaki M.Sato T.Nakamura N.Ikeda M. J. Org. Chem. 1993, 58: 2360 - 5a
Di Lena F.Matyjaszewski K. Prog. Polym. Sci. 2010, 35: 959 - 5b
Tang W.Kwak Y.Braunecker W.Tsarevsky NV.Coote ML.Matyjaszewski K. J. Am. Chem. Soc. 2008, 130: 10702 - 5c
Clark AJ.Battle GM.Hemings AM.Haddlenton DM.Bridge A. Tetrahedron Lett. 2001, 42: 2003 - 5d
Clark AJ.Filik RP.Thomas GH. Tetrahedron Lett. 1999, 40: 4885 - 6a
di Lena F.Chai CLL. Polym. Chem. 2010, 1: 922 - 6b
Lin CY.Coote ML.Gennaro A.Matyjaszewski K. J. Am. Chem. Soc. 2008, 130: 12762 - 6c
Lucchese B.Humphreys KJ.Lee D.-H.Incarvito CD.Sommer RD.Rheingold AL.Karlin KD. Inorg. Chem. 2004, 43: 5987 - 6d
Navon N.Burg A.Cohen H.van Eldik R.Meyerstein D. Eur. J. Inorg. Chem. 2002, 423 - 6e
Matyjaszewski K. Macromol. Symp. 1998, 1: 105 - 6f
Kochi JK. Angew. Chem. Int. Ed. 1988, 27: 1227 - 6g
Jenkins CL.Kochi JK. J. Am. Chem. Soc. 1972, 94: 856 - 6h
Kochi JK. Science 1967, 155: 415 - 7a
Motoyama Y.Hanada S.Shimamoto N.Nagashima H. Tetrahedron 2006, 62: 2779 - 7b
Iwamatsu S.Matsubara K.Nagashima H. J. Org. Chem. 1999, 64: 9625 - 7c
Benedetti M.Forti L.Ghelfi F.Pagnoni UM.Ronzoni R. Tetrahedron 1997, 53: 14031 - 7d
Curran DP.Tamine J. J. Org. Chem. 1991, 56: 2746 - 8a
Ghelfi F.Pattarozzi M.Roncaglia F.Parsons AF.Felluga F.Pagnoni UM.Valentin E.Mucci A.Bellesia F. Synthesis 2008, 3131 - 8b
Iwamatsu S.Kondo H.Matsubara K.Nagashima H. Tetrahedron 1999, 55: 1687 - 8c
Rachita MA.Slough GA. Tetrahedron Lett. 1993, 34: 6825 - 9a
Motoyama Y.Gondo M.Masuda S.Iwashita Y.Nagashima H. Chem. Lett. 2004, 33: 442 - 9b
Nagashima H.Wakamatsu H.Ozaki N.Ishii T.Watanabe M.Tajima T.Itoh K. J. Org. Chem. 1992, 57: 1682 - 10a
Pattarozzi M.Roncaglia F.Accorsi L.Parsons AF.Ghelfi F. Tetrahedron 2010, 66: 1357 - 10b
Ghelfi F.Stevens C.Laureyn I.Van Meenen E.Rogge TM.De Buyck L.Nikitin KV.Grandi R.Libertini MC.Pagnoni UM.Schenetti L. Tetrahedron 2003, 59: 1147 - 11a
Thommes K.Kiefer G.Scopelliti R.Severin K. Angew. Chem. Int. Ed. 2009, 48: 8115 - 11b
Forti L.Ghelfi F.Levizzani S.Pagnoni UM. Tetrahedron Lett. 1999, 40: 3233 - 11c
Baldovini N.Bertrand M.-P.Carrière A.Nougurier R.Plancher J.-M. J. Org. Chem. 1996, 61: 3205 - 12
Ishibashi H.Nakatani H.Iwami S.Sato T.Nakamura N.Ikeda M. J. Chem. Soc., Chem. Commun. 1989, 1767 - 13
Seijas JA.Vázquez-Tato MP.Castedo L.Estévez RJ.Ónega MG.Ruíz M. Tetrahedron 1992, 48: 1637 - 14
Casolari R.Felluga F.Frenna V.Ghelfi F.Pagnoni UM.Parsons AF.Spinelli D. Tetrahedron 2011, 67: 408 - 15a
Padmarani K.Kinoshita H.Inomata K. Bull. Chem. Soc. Jpn. 2000, 73: 497 - 15b
Clark AJ.Battle GM.Bridge A. Tetrahedron Lett. 2001, 42: 1999 - 16a
Muzart J. Tetrahedron 2009, 65: 8313 - 16b
Antonaccio LD.Serpa LMF.Wanderley W.Florio E. An. Acad. Bras. Ciênc. 1972, 44: 419 - 16c
Pizey JS. Synthetic Reagents Vol. 1: Wiley; New York: 1974. p.18-21 - 16d We deem that elimination
follows an E2H mechanism; for a different view, see:
Smith MB.March J. March’s Advanced Organic Chemistry Wiley; Hoboken: 2007. p.1495-1496 - 18a
Smith MB.March J. March’s Advanced Organic Chemistry Wiley; Hoboken: 2007. p.503 - 18b
Carey FA.Sundberg RJ. Advanced Organic Chemistry. Part A: Structure and Mechanisms Springer; New York: 2007. p.417-419 - 19a
Brzozowski Z.Slawiński J. Synth. Commun. 2010, 40: 1639 - 19b
Srinivasan S.Manisankar P. Synth. Commun. 2010, 40: 3538 - 19c
Obviously with NMP as reagent/solvent, no pressure build-up was observed.
- 20
Bruckner R. Advanced Organic Chemistry Harcourt-Academic Press; Burlington: 2002. p.140 - 21 The ATRC cyclization of N-allyl-N-Ts-α-monohaloamides is
noted, see ref. 11b and:
Clark AJ.Filik RP.Haddleton DM.Radigue A.Sanders CJ.Thomas GH.Smith ME. J. Org. Chem. 1999, 64: 8954 - 22a
Schnyder A.Beller M.Mehltretter G.Nsenda T.Studer M.Indolese AF. J. Org. Chem. 2001, 66: 4311 - 22b
Wan Y.Alterman M.Larhed M.Hallberg A.
J. Comb. Chem. 2003, 5: 82 - 23
Clark AJ.De Campo F.Deeth RJ.Filik RP.Gatard S.Hunt NA.Lastécouères D.Gerard HT.Verlhac J.-B.Wongtap H. J. Chem. Soc., Perkin Trans. 1 2000, 671 - 24
Moore GGI, andConway AC. inventors; US 3609187. ; Chem. Abstr. 1971, 75, 151529 - 25a
Whitehead CW.Traverso JJ. J. Am. Chem. Soc. 1958, 80: 2182 - 25b
Patel MC.Livinghouse T.Pagenkopf BL. Org. Synth. 2003, 80: 93 - 25c
Siska DP.Shriver DF. Chem. Mater. 2001, 13: 4698 - 26
Carlsen HJ.Jørgensen KB. J. Heterocycl. Chem. 1997, 34: 797
References
A small configuration reversal, unexploitable in practical terms, operated at C3 by MeONa during the functional rearrangement of 3-chloro-4-(chloromethyl)-1-(pyridinyl)- and -1-[(2-pyrimidyl)methyl]pyrrolidin-2-one in MeONa/MeOH.8a