Convenient chlorination of some special aromatic compounds using N-chlorosuccinimide

Synthesis

Volumn 44, Issue 7, 2012, Pages 1074-1078

  Gan, Zongjie ^a   Hu, Bin ^a   Song, Qiao ^a   Xu, Yungen ^a  

^a CHINA PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

benzofurans; carbazoles; chlorination; indoles; N chlorosuccinimide; pyridines

Indexed keywords

ANILINE DERIVATIVES; BENZOFURANS; CARBAZOLES; CHLORINATED AROMATIC COMPOUNDS; EFFICIENT SYNTHESIS; ENVIRONMENTALLY-FRIENDLY; FACILE PROCEDURE; HIGH YIELD; INDOLES; N-CHLOROSUCCINIMIDE; REACTION CONDITIONS;

AROMATIZATION; ELECTROPOLYMERIZATION; POLYCYCLIC AROMATIC HYDROCARBONS; PYRIDINE; SYNTHESIS (CHEMICAL);

CHLORINATION;

2 AMINO 5 CHLOROPYRIDINE; 2 CHLORO 3 NITROANILINE; 3 CHLORO 4 HYDROXYPYRIDINE; 3 CHLOROCARBAZOLE; 4 CHLORO 3 METHOXYANILINE; 5 CHLORO 2 HYDROXYPYRIDINE; AROMATIC COMPOUND; METHYL 2 CHLORO 1H INDOLE 3 CARBOXYLATE; METHYL 2 CHLOROBENZOFURAN 3 CARBOXYLATE; N CHLOROSUCCINIMIDE; SOLVENT; SUCCINIMIDE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHLORINATION; DRUG STRUCTURE; DRUG SYNTHESIS; PROCESS OPTIMIZATION; TEMPERATURE;

EID: 84862783280     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289732     Document Type: Article

References (30)

1. These authors contributed equally to this work.
2. Dewkar G K., Narina S V., Sudalai A, Org. Lett. 2003 5 4501
3. Yu G.-X, Mason H J., Galdi K, Wu X.-M, Cornelius L, Zhao N, Witkus M, Ewing W R., Macor J E., Synthesis 2003 403
4. Jayachandran B, Phukan P, Daniel T, Sudalai A, Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2006 45 972
5. U.S. Statutes. Clean Air Act Amendments of 1990 (Public Law 101-549).
6. Nickson T E., Roche-Dolson C A., Synthesis 1985 669
7. Bovonsombat P, Ali R, Khan C, Leykajarakul J, Pla-on K, Aphimanchindakul S, Pungcharoenpong N, Timsuea N, Arunrat A, Punpongjareorn N, Tetrahedron 2010 66 6928
8. Yamamoto T, Toyota K, Morita N, Tetrahedron Lett. 2010 51 1364
9. Zysman-Colman E, Arias K, Siegel J S., Can. J. Chem. 2009 87 440
10. Bartoli S, Cipollone A, Squarcia A, Madami A, Fattori D, Synthesis 2009 1035
11. Surya Prakash G K., Mathew T, Hoole D, Esteves P M., Wang Q, Rasul G, Olah G A., J. Am. Chem. Soc. 2004 126 15770
12. Kunzer A R., Wendt M D., Tetrahedron Lett. 2011 52 1815
13. Showalter H D. H., Sercel A D., Leja B M., Wolfangel C D., Ambroso L A., Elliott W L., Fry D W., Kraker A J., Howard C T., Lu G H., Moore C W., Nelson J M., Roberts B J., Vincent P W., Denny W A., Thompson A M., J. Med. Chem. 1997 40 413
14. Marchetti L, Andreani A, Ann. Chim. (Rome) 1973 63 681
15. Tang S, Li J.-H, Xie Y.-X, Wang N.-X, Synthesis 2007 1535
16. Yamada K, Kanbayashi Y, Tomioka S, Somei M, Heterocycles 2002 57 1627
17. Bogdal D, Lukasiewicz M, Pielichowski J, Green Chem. 2004 6 110
18. Bowyer P M., Iles D H., Ledwith A, J. Chem. Soc. C 1971 2775
19. Bonesi M S., Erra-Balsells R, J. Heterocycl. Chem. 1997 34 877
20. Orlov V Y., Begunov R S., Demidova N Y., Rusakov A I., Russ. J. Gen. Chem. 2006 76 76
21. Sonavane S U., Jayaram R V., Synth. Commun. 2003 33 843
22. Farhadi S, Kazem M, Siadatnasab F, Polyhedron 2011 30 606
23. Mohapatra S K., Sonavane S U., Jayaram R V., Selvam P, Tetrahedron Lett. 2002 43 8527
24. Farhadi S, Siadatnasab F, J. Mol. Catal. A: Chem. 2011 339 108
25. Stokes B J., Jovanovic B, Dong H.-J, Richert K J., Riell D R., Driver T G., J. Org. Chem. 2009 74 3225
26. Kalatzis E, Mastrokalos C, J. Chem. Soc., Perkin Trans. 2 1977 1835
27. Raju R R., Mohan S K., Reddy S J., Tetrahedron Lett. 2003 44 4133
28. Talik T, Rocz. Chem. 1963 37 69
29. Crowther A F., Curd F H. S., Davey D G., Hendry J A., Hepworth W, Rose F L., J. Chem. Soc. 1951 1774
30. Sbarbati N E., J. Org. Chem. 1965 30 3365