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 2022(3): 480-484
DOI: 10.1055/s-2004-834939
DOI: 10.1055/s-2004-834939
PAPER
© Georg Thieme Verlag Stuttgart · New York
Indium(III) Bromide: A Novel and Efficient Reagent for the Rapid Synthesis of 1,5-Benzodiazepines under Solvent-Free Conditions
Further Information
Received
27 July 2004
Publication Date:
01 December 2004 (online)
Publication History
Publication Date:
01 December 2004 (online)
Abstract
o-Phenylenediamines (OPDA) undergo rapid condensation with ketones having hydrogens at the α-position in the presence of 10 mol% indium(III) bromide under extremely mild reaction conditions to afford the corresponding 1,5-benzodiazepines in excellent yields with high selectivity. The remarkable features of this new procedure are high conversions, short reaction times, cleaner reaction profiles, high regioselectivity in the case of unsymmetrical ketones, solvent-free conditions, and simple experimental and work-up procedures. This method works well for both electron-rich as well as electron-deficient o-phenylenediamines.
Keywords
indium - ketones - heterocycles - benzodiazepines - solvent-free reaction - drugs
-
1a
Schutz H. Benzodiazepines Springer; Heidelberg: 1982. -
1b
Landquist JK. In Comprehensive Heterocyclic Chemistry Vol. 1:Katritzky AR.Rees CW. Pergamon; Oxford: 1984. p.166-170 -
1c
Fryer RI. Bicyclic Diazapines, In The Chemistry of Heterocyclic Compounds Vol. 50:Taylor EC. Wiley; New York: 1991. Chap. II. - 2
Randall LO.Kappel B. BenzodiazepinesGarattini S.Mussini E.Randall LO. Raven Press; New York: 1973. p.27 - 3
Haris RC, andStraley JM. inventors; U. S. Patent 1537757. ; Chem. Abstr. 1970, 73, 100054w - 4
De Baun JR,Pallos FM, andBaker DR. inventors; U. S. Patent 3978227. ; Chem. Abstr. 1977, 86, 5498d -
5a
Aversa MC.Ferlazzo A.Gionnetto P.Kohnke FH. Synthesis 1986, 230 -
5b
Essaber M.Baouid A.Hasnaoui A.Benharref A.Lavergne JP. Synth. Commun. 1998, 28: 4097 -
5c
El-Sayed AM.Abdel-Ghany H.El-Saghier AMM. Synth. Commun. 1999, 29: 3561 -
5d
Chimirri A.Grasso S.Ottana R.Romeo G.Zappala M. J. Heterocycl. Chem. 1990, 27: 371 -
6a
Stahlhofen P.Ried W. Chem. Ber. 1957, 90: 815 -
6b
Reid W.Torinus E. Chem. Ber. 1959, 92: 2902 -
6c
Herbert JAL.Suschitzky H. J. Chem. Soc., Perkin Trans. 1 1974, 2657 -
6d
Kaupp G.Pogodda U.Schmeyers J. Chem. Ber. 1994, 127: 2249 -
7a
Balakrishna MS.Kaboudin B. Tetrahedron Lett. 2001, 42: 1127 -
7b
Curini M.Epifano F.Marcotullio MC.Rosati O. Tetrahedron Lett. 2001, 42: 3193 -
7c
Morales HR.Bulbarela A.Contreras R. Heterocycles 1986, 24: 135 -
7d
Kaboudin B.Navaee K. Heterocycles 2001, 55: 1443 -
8a
Pozarentzi M.Stephanatou JS.Tsoleridis CA. Tetrahedron Lett. 2002, 43: 1755 -
8b
Reddy BM.Sreekanth PM. Tetrahedron Lett. 2003, 44: 4447 -
8c
Jarikote DV.Siddiqui SA.Rajagopal R.Daniel T.Lahoti RJ.Srinivasan KV. Tetrahedron Lett. 2003, 44: 1835 -
9a
Li CJ.Chan TH. Tetrahedron 1999, 55: 11149 -
9b
Babu G.Perumal PT. Aldrichima Acta 2000, 33: 16 -
9c
Ghosh R. Indian J. Chem. 2001, 40B: 550 -
10a
Ceschi MA.Felix LA.Peppe C. Tetrahedron Lett. 2000, 41: 9695 -
10b
Bandini M.Cozzi PG.Giocomini M.Melchiorre P.Selva S.Umani-Ronchi A. J. Org. Chem. 2002, 67: 3700 -
11a
Yadav JS.Reddy BVS. Synthesis 2002, 511 -
11b
Yadav JS.Reddy BVS.Raju AK.Rao CV. Tetrahedron Lett. 2002, 43: 5437 -
11c
Yadav JS.Reddy BVS.Satheesh G.Prabhakar A.Kunwar AC. Tetrahedron Lett. 2003, 44: 2221 -
11d
Yadav JS.Reddy BVS.Baishya G. Synlett 2003, 396