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 2009(21): 3642-3648
DOI: 10.1055/s-0029-1217004
DOI: 10.1055/s-0029-1217004
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
A New Approach to Methoxyisatins Leading to the Total Synthesis of Ophiuroidine and Other Hydroxytryptanthrins
Further Information
Received
9 June 2009
Publication Date:
08 September 2009 (online)
Publication History
Publication Date:
08 September 2009 (online)
Abstract
A new method for the preparation of methoxyisatins from the corresponding methoxyanilines is described. The resulting methoxyisatins were used in the syntheses of several methoxytryptanthrin compounds. The natural product ophiuroidine (4,8,9-trihydroxytryptanthrin) was obtained from the appropriate trimethoxy precursor using a microwave-mediated Prey demethylation.
Key words
isatin - tryptanthrin - ophiuroidine - Prey demethylation - microwave irradiation
- 1
Seidel P. Indigo-Studien BASF; Ludwigshafen: 1938. and references therein -
2a
Tafel J. Ber. Dtsch. Chem. Ges. 1892, 25: 1619 -
2b
Friedländer P.Roschdestwensky N. Ber. Dtsch. Chem. Ges. 1915, 48: 1841 -
2c
Machemer H. Ber. Dtsch. Chem. Ges. B. 1930, 63: 1341 -
2d
Heller G. Ber. Dtsch. Chem. Ges. B. 1936, 69: 563 -
2e
Bird CW. Tetrahedron 1963, 19: 901 - 3
Novotná P.Boon JJ.van der Horst J.Pacáková V. Color Technol. 2003, 119: 121 - 4
Witt A.Bergman J. Curr. Org. Chem. 2003, 7: 659 - 5
Utkina NK.Denisenko VA. Tetrahedron Lett. 2007, 48: 4445 - 6
Taylor A. J. Chem. Res., Miniprint 1980, 10: 4154 -
7a
Sumpter WC. Chem. Rev. 1954, 3: 393 -
7b
Popp FD. Adv. Heterocycl. Chem. 1975, 18: 2 -
7c
da Silva JFM.Garden SJ.Pinto AC. J. Braz. Chem. Soc. 2001, 12: 273 - 8
Kaila N.Janz K.DeBernardo S.Bedard PW.Camphausen RTJ.Tam S.Tsao DHH.Keith CK.Nickerson-Nutter C.Shilling A.Young-Sciame R.Wang Q. J. Med. Chem. 2007, 50: 21 - 9
Hewawasam P.Meanwell NA. Tetrahedron Lett. 1994, 35: 7303 - 10
Sadler PW. J. Org. Chem. 1956, 21: 169 - 11
Sharma VM.Prasanna P.Adi Sheshu KV.Renuka B.Laxman Rao CV.Sunil Kumar G.Prasad Narasimuhulu C.Arvind Babu P.Puranik RC.Subramanyam D.Venkateswarlu A.Rajagopal S.Sunil Kumar KB.Seshagiri Rao C.Rao Mamidi NVS.Deevi DS.Ajaykumar R.Rajagopalan R. Bioorg. Med. Chem. Lett. 2002, 12: 2303 - 12
Bergman J.Lindström J.Tilstam U. Tetrahedron 1985, 41: 2879 - 13
Tartar A.Gesquiere JC. J. Org. Chem. 1979, 44: 5000 -
14a
Prey V. Ber. 1941, 1219 -
14b
Wahlström N.Bergman J. Tetrahedron Lett. 2004, 45: 7273 -
14c
Protective
Groups in Organic Synthesis
3rd ed.:
Greene TW.Wuts PGM. John Wiley & Sons; New York: 1999. - 15
Kulkarni PP.Kadam AJ.Mane RB.Desai UV.Wadgaonk PP. J. Chem. Res., Synop. 1999, 394 -
16a
Wagner EC.Fegley MF. Org. Synth. 1917, 27: 15 -
16b
Hess HJ.Cronin TH.Scriabine A. J. Med. Chem. 1968, 11: 130 - 17
Sellstedt JH.Guinosso CJ.Begany AJ.Bell SC.Rosenthale M. J. Med. Chem. 1975, 18: 926 - 18
Love B.Jones H.Brown RE.Huang F.Khandwala A.Leibowitz MJ.Sonnino-Goldman P. J. Med. Chem. 1985, 28: 24 - 19
Cowell WT.Horner JK.Skinner WA. Public Bulletin Report, AD 435,889 United States Department of Commerce, Office of Technical Services; Washington, DC: 1964. - 20
Giovannini E.Portman P. Helv. Chim. Acta 1948, 31: 1381 - 21
Baker WL, andMitscher LA. inventors; PCT Int. Appl. WO 9513807, . ; Chem. Abstr. 1995, 123, 256757