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Journal of Heterocyclic Chemistry

Volumn 45, Issue 5, 2008, Pages 1481-1484

A three-component, one-pot synthesis of oxazinoquinolin-3-one derivatives

(4) Shakibaei, Gazaleh Imani a Khavasi, Hamid Reza a Mirzaei, Peiman a Bazgir, Ayoob a

a SHAHID BEHESHTI UNIVERSITY (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DIHYDRO 1 (2 CHLOROPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (2 METHOXYPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (3 BROMOPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (4 BROMOPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (4 CHLOROPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (4 FLUOROPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (4 METHOXYPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 (4 METHYLPHENYL) [1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; 1,2 DIHYDRO 1 PHENYL[1,3]OXAZINO[5,6 F]QUINOLIN 3 ONE; ALDEHYDE; QUINOLINE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DERIVATIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; MICROWAVE RADIATION; ONE POT SYNTHESIS; POLYMERIZATION;

EID: 51849143188 PISSN: 0022152X EISSN: None Source Type: Journal
DOI: 10.1002/jhet.5570450538 Document Type: Article

Times cited : (18)

References (23)

1
- 15844376844
- (a) Larsen R. D.; Corley E. G.; King A. O.; Carrol J. D.; Davis P.; Verhoeven T. R.; Reider P. J.; Labelle M.; Gauthier J. Y.; Xiang Y. B.; Zamboni R. J. J. Org. Chem. 1996, 61, 3398.
- (1996) J. Org. Chem , vol.61 , pp. 3398
- Larsen, R.D.¹ Corley, E.G.² King, A.O.³ Carrol, J.D.⁴ Davis, P.⁵ Verhoeven, T.R.⁶ Reider, P.J.⁷ Labelle, M.⁸ Gauthier, J.Y.⁹ Xiang, Y.B.¹⁰ Zamboni, R.J.¹¹

2
- 0035811449
- (b) Chen Y. L.; Fang K. C.; Shen J. Y.; Hsu S. L.; Tzeng C. C. J. Med. Chem. 2001, 44, 2374.
- (2001) J. Med. Chem , vol.44 , pp. 2374
- Chen, Y.L.¹ Fang, K.C.² Shen, J.Y.³ Hsu, S.L.⁴ Tzeng, C.C.⁵

3
- 0032580925
- (a) Kalluraya B.; Sreenivasa S. Farmaco 1998, 53, 399.
- (1998) Farmaco , vol.53 , pp. 399
- Kalluraya, B.¹ Sreenivasa, S.²

4
- 17544392459
- (b) Doube D.; Blouin M.; Brideau C.; Chan C.; Desmarais S.; Eithier D.; Falgueyret J. P.; Friesen R. W.; Girrard M.; Girard Y.; Guay J.; Tagari P.; Young R. N. Bioorg. Med. Chem. Lett. 1998, 8, 1255.
- (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 1255
- Doube, D.¹ Blouin, M.² Brideau, C.³ Chan, C.⁴ Desmarais, S.⁵ Eithier, D.⁶ Falgueyret, J.P.⁷ Friesen, R.W.⁸ Girrard, M.⁹ Girard, Y.¹⁰ Guay, J.¹¹ Tagari, P.¹² Young, R.N.¹³

5
- 0028243048
- Maguire M. P.; Sheets K. R.; McVety K.; Spada A. P.; Zilberstein A. J. Med. Chem. 1994, 37, 2129.
- (1994) J. Med. Chem , vol.37 , pp. 2129
- Maguire, M.P.¹ Sheets, K.R.² McVety, K.³ Spada, A.P.⁴ Zilberstein, A.⁵

6
- 0033571566
- (a) Patel M.; McHugh R. J.; Beverly Jr. Bioorg. Med. Chem. Lett. 1999, 9, 3221.
- (1999) Bioorg. Med. Chem. Lett , vol.9 , pp. 3221
- Patel, M.¹ McHugh, R.J.² Beverly, Jr.³

7
- 11244287919
- (b) El-Shafei H. A.; Badr-Eldin S. M. Egypt J. Microbiol. 1994, 27, 353.
- (1994) Egypt J. Microbiol , vol.27 , pp. 353
- El-Shafei, H.A.¹ Badr-Eldin, S.M.²

8
- 0033972803
- (c) Waxman L.; Darke P. L. Antiviral Chem. Chemother. 2000, 11, 1.
- (2000) Antiviral Chem. Chemother , vol.11 , pp. 1
- Waxman, L.¹ Darke, P.L.²

9
- 0005164801
- (d) Girgis A. S. Pharmazie 2000, 466.
- (2000) Pharmazie , pp. 466
- Girgis, A.S.¹

10
- 0019997677
- Latif N.; Mishriky N.; Assad F. M. Aust. J. Chem. 1982, 35, 1037.
- (1982) Aust. J. Chem , vol.35 , pp. 1037
- Latif, N.¹ Mishriky, N.² Assad, F.M.³

11
- 0033523619
- Patel M.; Ko S. S.; McHugh R. J. Jr.; Markwalder J. A.; Srivastava A. S.; Cordova B. C.; Klabe R. M.; Erickson-Viitanen S.; Trainor G. L.; Seitz S. P. Bioorg. Med. Chem. Lett. 1999, 9, 2805.
- (1999) Bioorg. Med. Chem. Lett , vol.9 , pp. 2805
- Patel, M.¹ Ko, S.S.² McHugh Jr., R.J.³ Markwalder, J.A.⁴ Srivastava, A.S.⁵ Cordova, B.C.⁶ Klabe, R.M.⁷ Erickson-Viitanen, S.⁸ Trainor, G.L.⁹ Seitz, S.P.¹⁰

12
- 85007952708
- (a) Ikeda K.; Morimoto T.; Sekia M. Chem. Pharm. Bull. 1980, 1178.
- (1980) Chem. Pharm. Bull , pp. 1178
- Ikeda, K.¹ Morimoto, T.² Sekia, M.³

13
- 8644226045
- (a) Yadav L. D. S.; Kapoor R. J. Org. Chem. 2004, 69, 8118.
- (2004) J. Org. Chem , vol.69 , pp. 8118
- Yadav, L.D.S.¹ Kapoor, R.²

14
- 2542489586
- (b) Yadav L. D. S.; Saigal S.; Pal D. R. J. Chem. Res. (S) 1998, 307.
- (1998) J. Chem. Res. (S) , pp. 307
- Yadav, L.D.S.¹ Saigal, S.² Pal, D.R.³

15
- 11244305953
- Cimarelli C.; Palmieri G.; Volpini E. Can. J. Chem. 2004, 82, 1314.
- (2004) Can. J. Chem , vol.82 , pp. 1314
- Cimarelli, C.¹ Palmieri, G.² Volpini, E.³

16
- 18544412716
- Szatmari I.; Hetenyi A.; Lazar L; Fulop F. J. Heterocycl. Chem. 2004, 41, 367.
- (2004) J. Heterocycl. Chem , vol.41 , pp. 367
- Szatmari, I.¹ Hetenyi, A.² Lazar, L.³ Fulop, F.⁴

17
- 33947730183
- Dabiri, M.; Delbari, A. S., Bazgir, A. Synlett 2007, 821
- (2007) Synlett , pp. 821
- Dabiri, M.¹ Delbari, A.S.² Bazgir, A.³

18
- 0030732273
- (a) Kappe, C. O. J. Org. Chem. 1997, 62, 7201.
- (1997) J. Org. Chem , vol.62 , pp. 7201
- Kappe, C.O.¹

19
- 24044514966
- (b) Huang, S.; Pan, Y.; Zhu, Y.; Wu, A. Org. Lett. 2005, 7, 3797.
- (2005) Org. Lett , vol.7 , pp. 3797
- Huang, S.¹ Pan, Y.² Zhu, Y.³ Wu, A.⁴

20
- 0037492348
- (c) Cristau, P.; Vors, J.; Zhu, J. P. Tetrahedron Lett. 2003, 44, 5575.
- (2003) Tetrahedron Lett , vol.44 , pp. 5575
- Cristau, P.¹ Vors, J.² Zhu, J.P.³

21
- 1242328670
- (d) Dondoni, A.; Massi, A.; Minghini, E.; Bertolasi, V. Tetrahedron 2004, 60, 2311.
- (2004) Tetrahedron , vol.60 , pp. 2311
- Dondoni, A.¹ Massi, A.² Minghini, E.³ Bertolasi, V.⁴

22
- 51849143499
- Crystal data analyses: Stoe IPDS-II two-circle diffractometer, MoK α radiation (λ, 0.71073, T =293(2) K; Graphite monochromator; numerical absorption correction. Structure solution by direct methods using SHELXS and refinement by full-matrix least-squares on F 2 using SHELXL of the X-STEP32 suite of programs [14] all non-hydrogen atoms were refined anisotropically. Crystal data for 4b: C17H11ClN2O2.(CH3) 2SO, M, 387.86 gmol-1; crystal dimensions 0.30 x 0.25 x 0.20 mm3; Triclinic, space group P1, Z=2; a, 8.7331(17, b, 9.1208(18, c, 13.834(3) Å, α, 72.82(3)°, β, 89.37(3)°, γ, 64.76(3)°; V, 943.8(3) Å3; F000, 402, ρcalc, 1.365 g cm-3; 2. 57°<θ<29.32°; section of the reciprocal lattice: -9 ≤ h ≤ 12, 12 ≤ k ≤ 12, 16 ≤ 1 ≤ 18; of 1
- -3). Crystallographic data for 4b have been deposited with the Cambridge Crystallographic Data Centre. Copies of the data can be obtained, free of charge, on application to The Director, CCDC 664117, Union Road, Cambridge CB2 1EZ, UK. Fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk.

23
- 51849102679
- X-STEP32 Version 1.07b, X-ray structure evaluation package, 2000, Stoe & Cie, Darm-stadt, Germany
- X-STEP32 Version 1.07b, X-ray structure evaluation package, 2000, Stoe & Cie, Darm-stadt, Germany.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.