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Synthesis 2017; 49(12): 2683-2690
DOI: 10.1055/s-0036-1588742
DOI: 10.1055/s-0036-1588742
paper
Synthesis of Multisubstituted 1,4-Dihydrobenzoxazin-2-ones through a One-Pot Nucleophilic N-Alkylation/C-Alkylation of Cyclic α-Imino Esters
Further Information
Publication History
Received: 03 January 2017
Accepted after revision: 17 February 2017
Publication Date:
09 March 2017 (online)

Abstract
A nucleophilic N-alkylation of 2-oxobenzoxazine-2-carboxylates with organozinc reagents with good selectivities and in moderate to good yields is described. Moreover, the synthesis of multisubstituted 1,4-dihydrobenzoxazine-2-ones bearing a tetrasubstituted carbon atom via a one-pot N-alkylation/C-alkylation reactions is reported.
Key words
dihydrobenzoxazinone - umpolung - zinc - tetrasubstituted carbon - one-pot reaction - cyclic α-imino estersSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0036-1588742.
- Supporting Information
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References
- 1a Ilaš J, Anderluh PŠ, Dolenc MS, Kikelj D. Tetrahedron 2005; 61: 7325-7325
- 1b Achari B, Mandal SB, Dutta PK, Chowdhury C. Synlett 2004; 2449-2449
- 1c Patel M, McHush RJ, Cordova BC, Klabe RM, Erickson-Viitanen S, Trainor GL, Rodgers JD. Bioorg. Med. Chem. Lett. 2000; 10: 1729-1729
- 1d Pamerla M, Reddy DR. S, Battula S, Bodipati N, Murthy YL. N. Med. Chem. Res. 2015; 24: 611-611
- 1e Bouyssou T, Casarosa P, Naline E, Pestel S, Konetzki I, Devillier P, Schnapp A. J. Pharmacol. Exp. Ther. 2010; 334: 53-53
- 1f Liu C, Tan JL, Xiao SY, Liao JF, Zou GR, Ai XX, Chen JB, Xiang Y, Yang Q, Zuo H. Chem. Pharm. Bull. 2014; 62: 915-915
- 1g Combs DW, Rampulla MS, Bell SC, Klaubert DH, Tobia AJ, Falotico R, Haertlein B, Lakas-Weiss C, Moore JB. J. Med. Chem. 1990; 33: 380-380
- 1h Blass B. ACS Med. Chem. Lett. 2013; 4: 1020-1020
- 1i Ilaš J, Jakopin Ž, Borštnar T, Stegnar M, Kikelj D. J. Med. Chem. 2008; 51: 5617-5617
- 1j Moffett RB. J. Med. Chem. 1966; 9: 475-475
- 2 Miles DH, Petrovna KO, Naser S, Yurjevich SS, Goun EA, Michailovich SV. US Patent 6 649 610, 2003
- 3 Lestage P, Lockhart B, Fleury MB, Largeron M. WO Patent Appl. 03033481, 2003
- 4a Sanna P, Carta A, Loriga M, Zanetti S, Sechi L. Farmaco 1999; 54: 161-161
- 4b Balzarini J, De Clercq E, Carbonez A, Burt V, Kleim J.-P. AIDS Res. Hum. Retroviruses 2000; 16: 517-517
- 4c Goldfarb DS. US Patent Appl. Publ. US 20090163545A1 20090625, 2009
- 5 Tanimori S, Nishimira T, Kirihata M. Bioorg. Med. Chem. Lett. 2009; 19: 4119-4119
- 6 Abu Shuheil MY, Hassuneh MR, Al-Hiari YM, Qaisi AM, El-Abadelah MM. Heterocycles 2007; 71: 2155-2155
- 7a Li X, Liu N, Zhang H, Knudson SE, Slayden RA, Tonge PJ. Bioorg. Med. Chem. Lett. 2010; 20: 6306-6306
- 7b Semenova TD, Krasnykh OP. Russ. J. Org. Chem. 2005; 41: 1222-1222
- 7c Zykova SS, Karmanova OG. Pharm. Chem. J. 2015; 49: 362-362
- 7d Venable JD, Kindrachuk DE, Peterson ML, Edwards JP. Tetrahedron Lett. 2010; 51: 337-337
- 7e Koz’minykh O, Goncharov VI, Koz’minykh EN. Russ. J. Org. Chem. 2006; 42: 1715-1715
- 7f Yao Q.-C, Wu D.-E, Ma R.-Z, Xia M. J. Organomet. Chem. 2013; 743: 1-1
- 7g López-Iglesias M, Busto E, Gotor V, Gotor-Fernández V. J. Org. Chem. 2015; 80: 3815-3815
- 7h Konda S, Raparti S, Bhaskar K, Munaganti RK, Guguloth V, Nagarapu L, Akkewar DM. Bioorg. Med. Chem. Lett. 2015; 25: 1643-1643
- 7i Nguyen KM. H, Schwendimann L, Gressens P, Largeron M. Org. Biomol. Chem. 2015; 13: 3749-3749
- 7j Ramesh C, Raju BR, Kavala V, Kuo C.-W, Yao C.-F. Tetrahedron 2011; 67: 1187-1187
- 8a Alapour S, Ramjugernathand D, Koorbanally NA. RSC Adv. 2015; 5: 83576-83576
- 8b Liu Z.-T, Wang Y.-H, Zhu F.-L, Hu X.-P. Org. Lett. 2016; 18: 1190-1190
- 8c Li D, Ma H, Yu W. Adv. Synth. Catal. 2015; 357: 3696-3696
- 8d Balalaie S, Bararjanian M, Hosseinzadeh S, Rominger F, Bijanzadeh HR, Wolf E. Tetrahedron 2011; 67: 7294-7294
- 8e Tanimori S, Inaba U, Kato Y, Ura H, Kashiwagi H, Nishimura T, Kirihata M. Res. Chem. Intermed. 2014; 40: 2157-2157
- 8f Luo X, Chenard E, Martens P, Cheng Y.-X, Tomaszewski MJ. Org. Lett. 2010; 12: 3574-3574
- 8g Luo X, Chenard E, Martens P, Srikanth Y.-G, Ramakrishna KV. S, Sharma GV. M. Org. Lett. 2015; 17: 4576-4576
- 9a Lou H, Wang Y, Jin E, Lin X. J. Org. Chem. 2016; 81: 2019-2019
- 9b Wu L.-L, Xiang Y, Yang D.-C, Guanand Z, He Y.-H. Catal. Sci. Technol. 2016; 6: 3963-3963
- 9c Wang Y.-Q, Zhang Y, Pan K, You J, Zhao J. Adv. Synth. Catal. 2013; 355: 3381-3381
- 9d Shinkevich EY, Novikov MS, Khlebnikov AF. Synthesis 2007; 225-225
- 9e Banzatti C, Heidempergher F, Melloni P. J. Hetererocycl. Chem. 1983; 20: 259-259
- 9f Shao P.-L, Liao J.-Y, Ho YA, Zhao Y. Angew. Chem. Int. Ed. 2014; 53: 5435-5435
- 9g Miyabe H, Yamaoka Y, Takemoto Y. Synlett 2004; 2597-2597
- 9h Xue Z.-Y, Jiang Y, Peng X.-Z, Yuan W.-C, Zhang X.-M. Adv. Synth. Catal. 2010; 352: 2132-2132
- 9i Yu J.-S, Zhou J. Org. Biomol. Chem. 2015; 13: 10968-10968
- 9j Kano T, Takechi R, Kobayashi R, Maruoka K. Org. Biomol. Chem. 2014; 12: 724-724
- 9k Kano T, Song S, Kubota Y, Maruoka K. Angew. Chem. Int. Ed. 2012; 51: 1191-1191
- 10a Fiaud J.-C, Kagan HB. Tetrahedron Lett. 1970; 11: 1813-1813
- 10b Fiaud J.-C, Kagan HB. Tetrahedron Lett. 1971; 12: 1019-1019
- 11a Münster P, Steglich W. Synthesis 1987; 223-223
- 11b Ermert P, Meyer J, Stucki C, Schneebeli J, Obrecht J.-P. Tetrahedron Lett. 1988; 29: 1265-1265
- 11c Calí P, Begtrup M. Synthesis 2002; 63-63
- 11d Chiev KP, Roland S, Mangeney P. Tetrahedron: Asymmetry 2002; 13: 2205-2205
- 11e Basra S, Fennie MW, Kozlowski MC. Org. Lett. 2006; 8: 2659-2659
- 11f Mitani M, Tanaka Y, Sawada A, Misu A, Matsumoto Y. Eur. J. Org. Chem. 2008; 1383-1383
- 11g Lin L, Fu X, Ma X, Zhang J, Wang R. Synlett 2012; 23: 2559-2559
- 11h Hatano M, Yamashita K, Mizuno M, Ito O, Ishihara K. Angew. Chem. Int. Ed. 2015; 54: 2707-2707
- 11i Yamamoto Y, Nishii S, Maruyama K, Komatsu T, Ito W. J. Am. Chem. Soc. 1986; 108: 7778-7778
- 12a Dickstein JS, Kozlowski MC. Chem. Soc. Rev. 2008; 37: 1166-1166
- 12b Shimizu M, Hachiya I, Mizota I. Chem. Commun. 2009; 874-874
- 12c Koyama K, Mizata I, Shimizu M. Pure Appl. Chem. 2014; 86: 755-755
- 13a Niwa Y, Takayama K, Shimizu M. Bull. Chem. Soc. Jpn. 2002; 75: 1819-1819
- 13b Niwa Y, Takayama K, Shimizu M. Tetrahedron Lett. 2001; 42: 5473-5473
- 13c Mizota I, Matsuda Y, Kamimura S, Tanaka H, Shimizu M. Org. Lett. 2013; 15: 4206-4206
- 13d Mizota I, Maeda T, Shimizu M. Tetrahedron 2015; 71: 5793-5793
- 13e Dickstein JS, Fennie MW, Norman AL, Paulose BJ, Kozlowski MC. J. Am. Chem. Soc. 2008; 130: 15794-15794
- 13f Curto JM, Dickstein JS, Berritt S, Kozlowski MC. Org. Lett. 2014; 16: 1948-1948
- 13g Curto JM, Kozlowski MC. J. Org. Chem. 2014; 79: 5359-5359
- 13h Mizutani Y, Tanimoto H, Morimoto T, Nishiyama Y, Kakiuchi K. Tetrahedron Lett. 2012; 53: 5903-5903
- 13i Tanaka H, Mizota I, Shimizu M. Org. Lett. 2014; 16: 2276-2276
- 13j Hatano M, Yamashita K, Ishihara K. Org. Lett. 2015; 17: 2412-2412
- 13k Yoo S.-E, Gong Y.-D. Heterocycles 1997; 45: 1251-1251
- 14a Niwa Y, Shimizu M. J. Am. Chem. Soc. 2003; 125: 3720-3720
- 14b Shimizu M, Takao Y, Katsurayama H, Mizota I. Asian J. Org. Chem. 2013; 2: 130-130
- 14c Sano T, Mizota I, Shimizu M. Chem. Lett. 2013; 42: 995-995
- 14d Mizota I, Tanaka K, Shimizu M. Tetrahedron Lett. 2012; 53: 1847-1847
- 14e Shimizu M, Niwa Y. Tetrahedron Lett. 2001; 42: 2829-2829
- 14f Yamamoto Y, Ito W. Tetrahedron 1988; 44: 5415-5415
- 15a van Vliet MR. P, Jastrzebski J, Klaver WJ, Goubitz K, van Koten G. Recl. Trav. Chim. Pays-Bas 1987; 106: 132-132
- 15b van der Steen FH, Kleijn H, Jastrzebski TB. H, van Koten G. J. Org. Chem. 1991; 56: 5147-5147
- 15c Uneyama K, Yan F, Hirama S, Katagiri T. Tetrahedron Lett. 1996; 37: 2045-2045
- 16 For a recent tandem N-alkylation/C-alkylation of quinoxalinone derivatives using Grignard reagents, see: Miyamaru S, Umezu K, Ito A, Shimizu M. Eur. J. Org. Chem. 2015; 3327-3327
- 17 For a C-selective alkylation of cyclic α-imino esters, see: Harwood LM, Vines KJ, Drew MG. B. Synlett 1996; 1051-1051
- 18 When we tried the N-alkylation of quinoxaline derivatives with Me2Zn, full conversion was not achieved yielding a mixture of approximately 1:1 starting material/product that was difficult to purify by column chromatography.
- 19 Li D, Ma H, Yu W. Adv. Synth. Catal. 2015; 357: 3696-3696
For pioneering work of Kagan, see:
For selected C-selective alkylation of α-imino esters, see:
For a review, see:
For accounts, see:
With Grignard reagents:
With organoaluminum reagents:
With organozinc reagents: