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Synthesis 2003(8): 1231-1235
DOI: 10.1055/s-2003-39392
DOI: 10.1055/s-2003-39392
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York
Annulated 1,2,4-Triazoles. A Convenient Synthesis of Thieno[2,3-f][1,2,4]triazolo[1,5-a]azepines: A Novel Triheterocyclic Ring System
Weitere Informationen
Received
7 January 2003
Publikationsdatum:
26. Mai 2003 (online)
Publikationsverlauf
Publikationsdatum:
26. Mai 2003 (online)
Abstract
A synthetic approach to the previously unknown thieno[2,3-f][1,2,4]triazolo[1,5-a]azepine derivatives was efficiently accomplished by cycloaddition of the bicyclic 1-aza-2-azoniaallene salts 6, derived from 6,7-dihydrobenzo[b]thiophen-4(5H)-one hydrazones 4, to the triple bond of nitriles, followed by ring enlargement. The X-ray crystal diffraction analysis of the picrate 10a provided affirmative proof for the structural assignment made.
Key words
1-aza-2-azoniaallene cations - cycloaddition - nitriles - ring enlargement - thieno[2,3-f][1,2,4]triazolo[1,5-a]azepines
- 1
Moriwaki M,Kawakami Y,Koga Y,Okamoto H, andTerasawa M. inventors; Jpn. Kokai Tokkyo Koho JP 05345785. ; Chem. Abstr. 1994, 121, 300897 - 2
Yamamoto Y,Shindo M, andNakamura T. inventors; PCT Int. Appl. WO 9747622. ; Chem. Abstr. 1998, 128, 75427 - 3
Tanaka H,Kuroita T,Ishibuchi S,Ushio H,Futamura T,Ohasha Y, andYano K. inventors; PCT Int. Appl. WO 9703986. ; Chem. Abstr. 1997, 126, 199585 - 4
Janssens FE,Lacrampe JFA, andPilatte INC. inventors; PCT Int. Appl. WO 9413681. ; Chem. Abstr. 1994, 121, 205360 - 5
Tanaka H.Nakao T. J. Heterocycl. Chem. 1997, 34: 921 - 6
Gu ZQ.Wong G.Dominguez C.de-Costa BR.Rice KC.Skolnick P. J. Med. Chem. 1993, 36: 1001 - 7
Kawakami Y.Kitani H.Yuasa S.Abe M.Moriwaki M.Kagoshima M.Terasawa M.Tahara T. Eur. J. Med. Chem. 1996, 31: 683 - 8
Liu X.Liu Y.Wang Q.Zou J. Synth. Commun. 2000, 30: 119 - 9
Wang Q.Liu X.Li F.Ding Z.Tao F. Synth. Commun. 2002, 32: 1327 - 10
Liu X.Wang Q.Liu Y.Fan Y.Ding Z. Synthesis 2000, 435 - 11
Cho H.Matsuki S. Heterocycles 1996, 43: 127 - 12
Fieser LF.Kennelly RG. J. Am. Chem. Soc. 1935, 57: 1611 - 13
Napier RP.Chu C. Int. J. Sulfur Chem., Part A 1971, 1: 62 - 14
Kajigaeshi S.Kakinami T.Moriwaki M.Fujisaki S.Maeno K.Okamoto T. Synthesis 1989, 545 - 15
Gstach H.Seil P. Synthesis 1990, 803 - 16
Wang Q.Jochims JC.Köhlbrandt S.Dahlenburg L.Al-Talib M.Hamed A.Ismail AE. Synthesis 1992, 710 - 17
Allen FH.Kennard O.Watson DG.Brammer L.Orpen AG.Taylor R. J. Chem. Soc., Perkin Trans. 2 1987, 12: S1 - 18
Dewar MJS.Thiel W. J. Am. Chem. Soc. 1977, 99: 4907 - 19
Ding Z.Xia S.Ji X.Yang H.Tao F.Wang Q. Synthesis 2002, 349 - 20
Mintz MJ.Walling C. Org. Synth., Coll. Vol. V Wiley; New York: 1973. p.184