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(11): 1897-1903
DOI: 10.1055/s-0028-1088048
DOI: 10.1055/s-0028-1088048
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Complementary Synthetic Approaches to Constitutionally Diverse N-Aminoalkylated Isoindolinones: Application to the Synthesis of Falipamil and 5-HT1A Receptor Ligand Analogues
Further Information
Received
21 January 2009
Publication Date:
14 April 2009 (online)
Publication History
Publication Date:
14 April 2009 (online)
Abstract
Different synthetic approaches for the elaboration of poly and diversely substituted isoindolinones tailed with constitutionally diverse aminoalkylated chains have been developed. The key step is based upon the preliminary assembly of the isoindolinone template equipped with hydroxyalkyl appendages. Subsequent manipulation of the terminal hydroxy functionality afforded the targeted compounds and the synthetic utility of these approaches has been emphasized by the synthesis of the bradycardic agent falipamil and 5-HT1A receptor ligand analogues.
Key words
carbanions - metalation - lactams - ring closure - ring opening
-
1a
Zhao XZ.Semenova EA.Vu BC.Maddali K.Marchand C.Hughes SH.Pommier Y.Burke TR. J. Med. Chem. 2008, 51: 251 -
1b
Maugeri C.Alisi MA.Apicella C.Cellai L.Dragone P.Fioravanzo E.Florio S.Furlotti G.Mangano G.Ombrato R.Luisi R.Pompei R.Rincicotti V.Russo V.Vitiello M.Cazzolla N. Bioorg. Med. Chem. 2008, 16: 3091 -
1c
Govindachari TR.Ravindranath KR.Viswanathan N. J. Chem. Soc., Perkin Trans. 1 1974, 1215 -
1d
Pendrak I.Barney S.Wittrock R.Lambert DM.Kingsbury WD. J. Org. Chem. 1994, 59: 2623 -
1e
Yeo H.Li Y.Fu L.Zhu J.-L.Gullen EA.Dutschman GE.Lee Y.Chung R.Huang E.-S.Austin DJ.Cheng Y.-C. J. Med. Chem. 2005, 48: 534 -
2a
Taylor EC.Zhou P.Jennings LD.Mao Z.Hu B.Jun J.-G. Tetrahedron Lett. 1997, 38: 521 -
2b
Fuska J.Fuskova A.Proksa B. Zb. Pr. Chemickotechnol Fak, SVST 1979-1981 (pub. 1986), 285 ; Chem. Abstr. 1987, 106, 95582 -
3a
Zeldis JB. inventors; PCT Int. Appl. WO 043378, . ; Chem. Abstr. 2004, 140, 417925 -
3b
Hardcastle IR.Ahmed SU.Atkins H.Calvert AH.Curtin NJ.Farnie G.Golding BT.Griffin RJ.Guyenne S.Hutton C.Källblad P.Kemp SJ.Kitching MS.Newell DR.Norbedo S.Northen JS.Reid RJ.Saravanan K.Willems HMG.Lunec J. Bioorg. Med. Chem. Lett. 2005, 15: 1515 -
3c
Shinji C.Maeda S.Imai K.Yoshida M.Hashimoto Y.Miyachi H. Bioorg. Med. Chem. 2006, 14: 7625 -
4a
Linden M.Hadler D.Hofmann S. Hum. Psychopharmacol. 1997, 12: 445 -
4b
Zhuang Z.-P.Kung M.-P.Mu M.Kung HF. J. Med. Chem. 1998, 41: 157 -
4c
Norman MH.Minick DJ.Rigdon GC. J. Med. Chem. 1996, 39: 149 - 5
Lippmann W. inventors; US Patent 4 267 189, . ; Chem. Abstr. 1981, 95, 61988 - 6
Lee HJ.Lim SJ.Oh SJ.Moon DH.Kim DJ.Tae J.Yoo KH. Bioorg. Med. Chem. Lett. 2008, 18: 1628 -
7a
Hamprecht D.Micheli F.Tedesco G.Checchia A.Donati D.Petrone M.Terreni S.Wood M. Bioorg. Med. Chem. Lett. 2007, 17: 428 -
7b
Cappelli A.Anzini M.Vomero S.Mennuni L.Makovec F.Doucet E.Hamon M.Menziani MC.De Benedetti PG.Giorgi G.Ghelardini C.Collina S. Bioorg. Med. Chem. 2002, 10: 779 - 8
Shinozuka T.Yamamoto Y.Hasegawa T.Saito K.Naito S. Tetrahedron Lett. 2008, 49: 1619 - 9
Reiffen M.Eberlein W.Mueller P.Psiorz M.Noll K.Heider J.Lillie C.Kobinger W.Luger P. J. Med. Chem. 1990, 33: 1496 -
10a
Dai-Ho G.Mariano PS. J. Org. Chem. 1987, 52: 704 -
10b
Lorion M.Couture A.Deniau E.Grandclaudon P. Synthesis 2008, 2141 - 11
Sarabu R.Cooper JP.Cook CM.Cook CM.Gillespie P.Perrotta AV.Olson GL. Drug Des. Discov. 1998, 15: 191 - 12
Lillie C.Kobinger W. J. Cardiovasc. Pharmacol. 1983, 5: 1048 -
13a
Brachmann J.Senges J.Hammann HD.Anders G.Beck L.Braun W.Kubler W. Z. Kardiol. 1979, 68: 635 -
13b
Daemmgen JW.Kadatz R.Diederen W. Arzneim.-Forsch. (Drug Res.) 1981, 31: 666 -
14a
Gross GJ.Daemmgen JW. J. Cardiovasc. Pharmacol. 1987, 10: 123 -
14b
Diederen W.van Meel JCA. J. Mol. Cell. Cardiol. 1986, 18 (Suppl. 2): 16 -
14c
Trach V.Daemmgen JW. J. Mol. Cell. Cardiol. 1986, 18 (Suppl. 2): 20 -
14d
Gross GJ.Daemmgen JW. J. Pharmacol. Exp. Ther. 1986, 238: 422 -
14e
Wenger HC.Siegl PKS. J. Cardiovasc. Pharmacol. 1987, 9: 246 -
14f
Siegl PKS.Morgan G. Can. J. Physiol. Pharmacol. 1987, 65: 146 -
14g
Siegl PKS.Wenger HC.Sweet CS. J. Cardiovasc. Pharmacol. 1984, 6: 565 -
15a
Levy S.Metge M.Hilaire J.Cointe R.Bru P.Eychenne JL.Grerard R. Eur. Heart J. 1987, 8: 1236 -
15b
Tryba M.Zenz M. Arzneim.-Forsch. (Drug Res.) 1987, 37: 1298 -
15c
Jost S.Schulz W.Kober G. Arzneim.-Forsch. (Drug Res.) 1985, 35 (II): 1279 -
15d
Herzog H.Simon H. Herz-Kreislauf 1983, 7: 354 -
15e
Gulker H. Eur. Heart J. 1987, 8 (Suppl. L): 141 -
15f
Gilfrich HJ.Oberhoffer M.Witzke J. Eur. Heart J. 1987, 8 (Suppl. L): 147 -
15g
Hilaire J.Broustet JP.Colle JP.Theron M. Br. J. Clin. Pharmacol. 1983, 16: 627 - 16
Siegl PKS.Morgan G. Can. J. Physiol. Pharmacol. 1987, 65: 146 - 17
Nakasaki M.Yamagami K.Isoe S. Bull. Chem. Soc. Jpn. 1961, 34: 1189 - 18
Lipshutz BH.Liu Z.-P.Kayser F. Tetrahedron Lett. 1994, 35: 5567 - 19
Dai-Ho G.Mariano PS. J. Org. Chem. 1987, 52: 704 - 20
Chauncey DM.Andrews LJ.Keefer RM. J. Am. Chem. Soc. 1974, 96: 1850 - 21
Olivera R.SanMartin R.Dominguez E.Solans X.Urtiaga MK.Arriortua MI. J. Org. Chem. 2000, 65: 6398 - 22
Markaryan EA.Markaryan RE.Arustamyan ZS.Airepetyan GK.Sukasyan RS.Markaryan KZ.Asatryan TO. Pharm. Chem. J. 1997, 31: 13 - 23
Lu Y.Taylor RT. Heterocycles 2004, 62: 869 - 24
Murata K. Bull. Chem. Soc. Jpn. 1973, 46: 1752