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Synthesis 2016; 48(24): 4541-4547
DOI: 10.1055/s-0036-1588308
DOI: 10.1055/s-0036-1588308
paper
Facile Synthesis of 3-Arylidene-3H-1,4-benzodiazepines by a Sequential Ugi/Staudinger/Aza-Wittig Reaction
Further Information
Publication History
Received: 10 August 2016
Accepted after revision: 12 August 2016
Publication Date:
14 September 2016 (online)
Abstract
N-[2-(Alkylamino)-1-(2-azidophenyl)-2-oxoethyl]-N-(3-oxoprop-1-en-2-yl)amides, obtained from the Ugi reaction of a vinyliminophosphorane, 2-azidobenzaldehyde, a carboxylic acid, and an alkyl isocyanide, reacted with triphenylphosphine to give various 3-arylidene-3H-1,4-benzodiazepine in good yields via sequential Staudinger and intramolecular aza-Wittig reaction.
Key words
3H-1,4-benzodiazepine - Ugi reaction - Staudinger reaction - aza-Wittig reaction - vinyliminophosphorane - azidesSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0036-1588308.
- Supporting Information
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References
- 1 Rivas FM, Stables JP, Murphree L, Edwankar RV, Edwankar CR, Huang S, Jain HD, Zhou H, Majumder S, Sankar S, Roth BL, Ramerstorfer J, Furtmüller R, Sieghart W, Cook JM. J. Med. Chem. 2009; 52: 1795
- 2 Anzini M, Braile C, Valenti S, Cappelli A, Vomero S, Marinelli L, Limongelli V, Novellino E, Betti L, Giannaccini G, Lucacchini A, Ghelardini C, Norcini M, Makovec F, Giorgi G, Fryer RI. J. Med. Chem. 2008; 51: 4730
- 3 Clark RL, Carter KC, Mullen AB, Coxon GD, Owusu-Dapaah G, McFarlane E, Thi MD. D, Grant MH, Tettey JN. A, Mackay SP. Bioorg. Med. Chem. Lett. 2007; 17: 624
- 4 Galli U, Travelli C, Aprile S, Arrigoni E, Torretta S, Grosa G, Massarotti A, Sorba G, Canonico PL, Genazzani AA, Tron GC. J. Med. Chem. 2015; 58: 1345
- 5a Liu J.-J, Higgins B, Ju G, Kolinsky K, Luk K.-C, Packman K, Pizzolato G, Ren Y, Thakkar K, Tovar C, Zhang Z, Wovkulich PM. ACS Med. Chem. Lett. 2013; 4: 259
- 5b Hunt JT, Ding CZ, Batorsky R, Bednarz M, Bhide R, Cho Y, Chong S, Chao S, Gullo-Brown J, Guo P, Kim SH, Lee FY. F, Leftheris K, Miller A, Mitt T, Patel M, Penhallow BA, Ricca C, Rose WC, Schmidt R, Slusarchyk WA, Vite G, Manne V. J. Med. Chem. 2000; 43: 3587
- 6 Nadin A, López JM. S, Owens AP, Howells DM, Talbot AC, Harrison T. J. Org. Chem. 2003; 68: 2844
- 7 Breslin HJ, Kukla MJ, Ludovici DW, Mohrbacher R, Ho W, Miranda M, Rodgers JD, Hitchens TK, Leo G, Gauthier DA, Ho CY, Scott MK, De Clercq E, Pauwels R, Andries K, Janssen MA. C, Janssen PA. J. J. Med. Chem. 1995; 38: 771
- 8a Katritzky AR, Xu Y.-J, He H.-Y. J. Chem. Soc., Perkin Trans. 1 2002; 592
- 8b Welmaker GS, Sebalski JE. Tetrahedron Lett. 2004; 45: 4851
- 9 Nguyen HH, Palazzo TA, Kurth MJ. Org. Lett. 2013; 15: 4492
- 10a Sañudo M, García-Valverde M, Marcaccini S, Delgado JJ, Rojo J, Torroba T. J. Org. Chem. 2009; 74: 2189
- 10b Pertejo P, Corres N, Torroba T, García-Valverde M. Org. Lett. 2015; 17: 612
- 10c Wang Y, Chen M, Ding MW. Tetrahedron 2013; 69: 9056
- 10d Lecinska P, Corres N, Moreno D, García-Valverde M, Marcaccini S, Torroba T. Tetrahedron 2010; 66: 6783
- 11a Rotstein BH, Zaretsky S, Rai V, Yudin AK. Chem. Rev. 2014; 114: 8323
- 11b Dömling A, Wang W, Wang K. Chem. Rev. 2012; 112: 3083
- 12a Azuaje J, Pérez-Rubio JM, Yaziji V, Maatougui AE, González-Gomez JC, Sańchez-Pedregal VM, Navarro-Vázquez A, Masaguer CF, Teijeira M, Sotelo E. J. Org. Chem. 2015; 80: 1533
- 12b Peshkov AA, Peshkov VA, Pereshivko OP, Van der Eycken EV. Tetrahedron 2015; 71: 3863
- 12c Patil P, Khoury K, Herdtweck E, Dömling A. Org. Lett. 2014; 16: 5736
- 12d Alvarez-Rodríguez NV, Dos Santos A, El Kaïm L, Gámez-Montaño R. Synlett 2015; 26: 2253
- 12e Vachhani DD, Kumar A, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. Synthesis 2015; 47: 1337
- 13a Kumar R, Ermolat’ev DS, Van der Eycken EV. J. Org. Chem. 2013; 78: 5737
- 13b Fesenko AA, Shutalev AD. Tetrahedron 2014; 70: 5398
- 13c Okamoto K, Shimbayashi T, Tamura E, Ohe K. Chem. Eur. J. 2014; 20: 1490
- 13d Hu Y, Li X, Wan B. Tetrahedron 2015; 71: 6935
- 13e Liu Y, Sun X, Zhang X, Liu J, Du Y. Org. Biomol. Chem. 2014; 12: 8453
- 13f Qu F, Hu R.-F, Gao L, Wu J, Cheng X.-H, Wang S, He P. Synthesis 2015; 47: 3701
- 14a Yang YY, Shou WG, Chen ZB, Hong D, Wang YG. J. Org. Chem. 2008; 73: 3928
- 14b Nishimura Y, Cho H. Synlett 2015; 26: 233
- 14c Wang L, Ren ZL, Chen M, Ding MW. Synlett 2014; 25: 721
- 14d Xie H, Yuan D, Ding MW. J. Org. Chem. 2012; 77: 2954
- 14e Nie YB, Wang L, Ding MW. J. Org. Chem. 2012; 77: 696
- 14f Xie H, Liu JC, Wu L, Ding MW. Tetrahedron 2012; 68: 7984
- 14g Xie H, Yu JB, Ding MW. Eur. J. Org. Chem. 2011; 6933