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 2005(18): 3063-3066
DOI: 10.1055/s-2005-916032
DOI: 10.1055/s-2005-916032
PAPER
© Georg Thieme Verlag Stuttgart · New YorkSynthesis of Novel Fatty Acid Derivatives of Etidronic Acid
Further Information
Received
14 April 2005
Publication Date:
29 September 2005 (online)
Publication History
Publication Date:
29 September 2005 (online)

Abstract
Synthesis of (1-acyloxyethylidene)-1,1-bisphosphonic acids, where the acyl group is decanoyl (1a), lauroyl (1b), palmitoyl (1c), stearoyl (1d) or oleoyl (1e) have been described. Preparation of (1-oleoyloxyethylidene)-1,1-bisphosphonic acid tetramethyl ester (2) and its P,P′-dimethyl ester (disodium salt 3 and acid form 4) in multigram scale has also been reported. Solubility of 1e in organic solvents and water was tested.
Key words
bisphosphonate - etidronate - fatty acids - synthesis - prodrug
- 1a
Fleisch H. Bisphosphonates in Bone Disease: From the Laboratory to the Patient The Parthenon Publishing Group Inc.; New York: 1995. - 1b
Papapoulos SE.Landman JO.Bijvoet OLM.Löwik CWGM.Valkema R.Pauwels EKJ.Vermeij P. Bone 1992, 13: S41 - 1c
Yates AJ.Rodan GA. DDT 1998, 3: 69 - 1d
Socrates E.Papapoulos MD. Am. J. Med. 1993, 95: 48S - 1e
Giannini S.D’Angelo AL.Sartori LG.Passeri G.Garbonare LD.Crebaldi C. Obst. Gynecol. 1996, 88: 431 - 2a
Szajnman SH.Montalvetti A.Wang Y.Docampo R.Rodriguez JB. Bioorg. Med. Chem. Lett. 2003, 13: 3231 - 2b
Szajnman SH.Bailey BN.Docampo R.Rodriguez JB. Bioorg. Med. Chem. Lett. 2001, 11: 789 - 2c
Martin MB.Sanders JM.Kendrick H.Luca-Fradley K.Lewis JC.Grimley JS.Van Brussel EM.Olsen JR.Meints GA.Burzynska A.Kafarski P.Croft SL.Oldfield E. J. Med. Chem. 2002, 45: 2904 - 2d
Garzoni LR.Caldera A.Nazareth L.Meirelles M.Castro SL.Docampo R.Meints GA.Oldfield E.Urbina JA. Int. J. Antimicrob. Agents 2004, 23: 273 - 2e
Garzoni LR.Waghabi MC.Baptista MM.Castro SL.Nazareth L.Meirelles M.Britto CC.Docampo R.Oldfield E.Urbina JA. Int. J. Antimicrob. Agents 2004, 23: 286 - 3
Ylitalo R. Gen. Pharmacol. 2002, 35: 287 - 4a
Vepsäläinen JJ. Curr. Med. Chem. 2002, 9: 1201 - 4b
Lin JH. Bone 1996, 18: 75 - 4c
Recker RR.Saville PD. Toxicol. Appl. Pharmacol. 1973, 24: 580 - 5a
Turhanen PA.Niemi R.Peräkylä M.Järvinen T.Vepsäläinen JJ. Org. Biomol. Chem. 2003, 1: 3223 - 5b
Ahlmark M.Vepsäläinen J.Taipale H.Niemi R.Järvinen T. J. Med. Chem. 1999, 42: 1473 - 5c
Niemi R.Vepsäläinen J.Taipale H.Järvinen T. J. Med. Chem. 1999, 42: 5053 - 5d
Niemi R.Turhanen P.Vepsäläinen J.Taipale H.Järvinen T. Eur. J. Pharm. Sci. 2000, 11: 173 - 5e
Turhanen PA.Ahlgren MJ.Järvinen T.Vepsäläinen JJ. Synthesis 2001, 633 - 5f
Turhanen PA.Vepsäläinen JJ. Synthesis 2004, 992 - 6
Turhanen PA.Vepsäläinen JJ. Synthesis 2005, 2119 - 8a
Pudovik AN.Konovalova IV. J. Gen. Chem. USSR 1963, 33: 91 - 8b
Pudovik AN.Gazizov TKh. J. Gen. Chem. USSR 1968, 38: 139 - 8c
Prentice JB.Quimby OT.Grabenstetter RJ.Nicholson DA. J. Am. Chem. Soc. 1972, 94: 6119 - 8d
Chopard PA. Helv. Chim. Acta 1967, 50: 1021 - 8e
Ruel R.Bouvier J.-P.Young RN. J. Org. Chem. 1995, 60: 5209 - 8f
Guenin E.Degache E.Liquier J.Lecouvey M. Eur. J. Org. Chem. 2004, 2983 - 9a
Nicholson DA.Vaughn H. J. Org. Chem. 1971, 36: 3843 - 9b
Turhanen PA.Ahlgren MJ.Järvinen T.Vepsäläinen JJ. Phosphorus, Sulfur Silicon Relat. Elem. 2001, 170: 115 - 10a
Mc Kenna CE.Shen P. J. Org. Chem. 1981, 46: 4573 - 10b
Vaghefi MM.Bernacki RJ.Hennen WJ.Robins RK. J. Med. Chem. 1987, 30: 1391 - 10c
Nguyen LM.Niesor E.Bentzen CL. J. Med. Chem. 1987, 30: 1426 - 10d
Ebetino FH.Degenhardt CR.Jamieson LA.Burdsall DC. Heterocycles 1990, 30: 855 - 10e
Nugent RA.Murphy M.Schlachter ST.Dunn CJ.Smith RJ.Staite ND.Galinet LA.Shields SK.Aspar DG.Richard KA.Rohloff NA. J. Med. Chem. 1993, 36: 134 - 11
Van Gelder JM.Breuer E.Ornoy A.Schlossman A.Patlas N.Golomb G. Bone 1995, 16: 511
References
Turhanen, P. A.; Vepsäläinen, J. J., Synthesis, submitted.