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 2013; 45(22): 3106-3117
DOI: 10.1055/s-0033-1338543
DOI: 10.1055/s-0033-1338543
paper
Biology- and Diversity-Oriented Domino Reactions for Synthesis of AMPA Receptor Antagonist IKM-159 and Analogues
Further Information
Publication History
Received: 02 August 2013
Accepted after revision: 19 August 2013
Publication Date:
12 September 2013 (online)

Abstract
By natural product inspired diversity-oriented synthesis, we had developed a new class of selective antagonist, IKM-159, for the AMPA receptor. Here, we report syntheses of IKM-159 and skeletally diverse five analogues in racemic forms, two of which are heterotricycles and the other three compounds are truncated analogues, to study the structure–activity relationships. The key reactions are two domino reactions including Ugi/Diels–Alder reaction and domino metathesis reaction. An exceptionally high level of regiocontrol in the cross metathesis reaction is also reported.
Key words
domino reaction - heterocycles - medicinal chemistry - metathesis - multicomponent reactionSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
References
- 2 Schreiber SL. Science 2000; 287: 1964
- 3 Burke MD, Schreiber SL. Angew. Chem. Int. Ed. 2004; 43: 46
- 4 Nielsen TE, Schreiber SL. Angew. Chem. Int. Ed. 2008; 47: 48
- 5 Nören-Müller A, Reis-Corrêa I, Prinz H, Rosenbaum C, Saxena K, Schwalbe HJ, Vestweber D, Cagna G, Schunk S, Schwarz O, Schiewe H, Waldmann H. Proc. Natl. Acad. Sci. U.S.A. 2006; 103: 10606
- 6a de Graaff C, Ruijter E, Orru RV. A. Chem. Soc. Rev. 2012; 41: 3969
- 6b Shiri M. Chem. Rev. 2012; 112: 3508
- 6c van Berkel SS, Bögels BG. M, Wijdeven MA, Westermann B, Rutjes FP. J. T. Eur. J. Org. Chem. 2012; 3543
- 7a Nicolaou KC, Chen JS. Chem. Soc. Rev. 2009; 38: 2993
- 7b Núñez MG, García P, Moro RF, Díez D. Tetrahedron 2010; 66: 2089
- 7c Grossmann A, Enders D. Angew. Chem. Int. Ed. 2012; 51: 314
- 7d Lu L.-Q, Chen J.-R, Xiao W.-J. Acc. Chem. Res. 2012; 45: 1278
- 8 Robinson R. J. Chem. Soc., Trans. 1917; 111: 762
- 9 Tietze LF. Chem. Rev. 1996; 96: 115
- 10 Oh CH, Karmakar S, Park H, Ahn Y, Kim JW. J. Am. Chem. Soc. 2010; 132: 1792
- 11 Dückert H, Pries V, Khedkar V, Menninger S, Bruss H, Bird AW, Maliga Z, Brockmeyer A, Janning P, Hyman A, Grimme S, Schürmann M, Preut H, Hübel K, Ziegler S, Kumar K, Waldmann H. Nat. Chem. Biol. 2012; 8: 179
- 12 Aydillo C, Jiménez-Osés G, Avenoza A, Busto JH, Peregrina JM, Zurbano MM. J. Org. Chem. 2011; 76: 6990
- 13 Hong B.-C, Nimje RY, Lin C.-W, Liao J.-H. Org. Lett. 2011; 13: 1278
- 14 Barluenga J, Mendoza A, Rodríguez F, Fañanás FJ. Angew. Chem. Int. Ed. 2008; 120: 7152
- 15 Hong B.-C, Kotame P, Tsai C.-W, Liao J.-H. Org. Lett. 2010; 12: 776
- 17 Akritopoulou-Zanze I, Djuric SW. Heterocycles 2007; 73: 125
- 18 Paulvannan K. Tetrahedron Lett. 1999; 40: 1851
- 19 Lee DS, Sello JK, Schreiber SL. Org. Lett. 2000; 2: 709
- 20a Oikawa M, Ikoma M, Sasaki M. Tetrahedron Lett. 2005; 46: 5863
- 20b Oikawa M, Ikoma M, Sasaki M. Tetrahedron Lett. 2005; 46: 415
- 20c Ikoma M, Oikawa M, Sasaki M. Tetrahedron 2008; 64: 2740
- 20d Ikoma M, Oikawa M, Sasaki M. Eur. J. Org. Chem. 2009; 72
- 21a Sakai R, Kamiya H, Murata M, Shimamoto K. J. Am. Chem. Soc. 1997; 119: 4112
- 21b Sakai R, Koike T, Sasaki M, Shimamoto K, Oiwa C, Yano A, Suzuki K, Tachibana K, Kamiya H. Org. Lett. 2001; 3: 1479
- 22 Parsons AF. Tetrahedron 1996; 52: 4149
- 23a Ikoma M, Oikawa M, Gill MB, Swanson GT, Sakai R, Shimamoto K, Sasaki M. Eur. J. Org. Chem. 2008; 5215
- 23b Oikawa M, Ikoma M, Sasaki M, Gill MB, Swanson GT, Shimamoto K, Sakai R. Eur. J. Org. Chem. 2009; 5531
- 23c Oikawa M, Ikoma M, Sasaki M, Gill MB, Swanson GT, Shimamoto K, Sakai R. Bioorg. Med. Chem. 2010; 18: 3795
- 24 Gill MB, Frausto S, Ikoma M, Sasaki M, Oikawa M, Sakai R, Swanson GT. Br. J. Pharmacol. 2010; 160: 1417
- 25 Juknaitė L, Sugamata Y, Tokiwa K, Ishikawa Y, Takamizawa S, Eng A, Sakai R, Pickering DS, Frydenvang K, Swanson GT, Kastrup JS, Oikawa M. J. Med. Chem. 2013; 56: 2283
- 26a Fukuyama T, Jow CK, Cheung M. Tetrahedron Lett. 1995; 36: 6373
- 26b Kan T, Fukuyama T. Chem. Commun. 2004; 353
- 27 Francais A, Bedel O, Haudrechy A. Tetrahedron 2008; 64: 2495
- 28 Takeuchi R, Tanabe K, Tanaka S. J. Org. Chem. 2000; 65: 1558
- 29 Garber SB, Kingsbury JS, Gray BL, Hoveyda AH. J. Am. Chem. Soc. 2000; 122: 8168
- 30a Weeresakare GM, Liu Z, Rainier JD. Org. Lett. 2004; 6: 1625
- 30b Liu Z, Rainier JD. Org. Lett. 2005; 7: 131
- 31a Kraus GA, Taschner MJ. J. Org. Chem. 1980; 45: 1175
- 31b Bal BS, Childers Jr WE, Pinnick HW. Tetrahedron 1981; 37: 2091
- 31c Dalcanale E, Montanari F. J. Org. Chem. 1986; 51: 567
- 32 Brown HC, Liu K.-T. J. Am. Chem. Soc. 1970; 92: 3502
- 33 Sakai, R., personal communication.
For recent reviews, see:
For recent reviews, see: