Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Patent
1995-04-03
1997-03-11
Marquis, Melvyn I.
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
549229, 560 56, 560174, 562463, 562577, C07D32100
Patent
active
056103140
ABSTRACT:
A process is provided for preparing dioxolenone derivatives of the structure ##STR1## wherein R is alkyl or aryl and R.sub.3 is CO.sub.2 R.sub.2 (where R.sub.2 is alkyl or arylalkyl such as benzyl, diphenylmethyl or para-methoxybenzyl). Intermediates produced in the above process are also provided as well as a method for preparing squalene synthetase inhibitors employing such intermediates.
REFERENCES:
Hiyama, T. et al, "The Photochemistry of 4,5-Disubstituted 1,3-Dioxolen-2-ones", Bull. Chem. Society of Japan, vol. 45, 2797-2801 (1972).
Ikeda, S. et al, "Studies on Prodrugs. III. A Convenient and Practical Preparation of Ampicillin Prodrugs", Chem. Pharm. Bull. vol. 32(11), 4316-4322 (1984).
Sakamoto, F. et al, "Studies on Prodrugs. II. Preparation and Characterization of (5-Substituted 2-Oxo-1,3-dioxolen-4-yl)methyl Esters of Ampicillin", Chem. Pharm. Bull. vol. 32(6) 2241-2248 (1984).
Ikeda, S. et al, "A Convenient and Practical Preparation of 4-Chloromethyl-5-methyl-1,3-dioxol-2-one", Chem. Pharm. Bull. vol. 36(1), 394-397 (1988).
Sakamoto, F. et al, "Studies on Prodrugs. VI. Preparation and Characterization of (5-Substituted 2-Oxo-1,3-dioxol-4-yl)methyl Esters of Mecillinam", Chem. Pharm. Bull., vol. 35(2), 642-646 (1987).
Sakamoto, F. et al, "Studies on Prodrugs. IV. Preparation and Characterization of N-(5-Substituted 2-oxo-1,3-dioxol-4-yl)methyl Norfloxacin", Chem. Pharm. Bull., vol. 33(11) 4870-4877 (1985).
Kawai, H. et al, "2-Oxo-1,3-dixoels as Specific Substrates for Measurement of Arylesterase Activity", Chem. Pharm. Bull., vol 39(6), 1422-1425 (1991).
Miyauchi, M. et al, "Studies on Penem and Carbapenem. II. An Improved Synthesis of Orally Active Penem Antibiotic (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl (5R,6S)-2-(2-Fluoroethylthio)-6-[(1R)-1-hydroxyethyl]penem-3-carboxylate", Chem. Pharm. Bull., vol. 38(4) 1077-1078 (1990).
Saari, W. S. et al, "3-Hydroxy-.alpha.-methyltyrosine Progenitors: Synthesis and evaluation of Some (2-Oxo-1,3-dioxol-4-yl)methyl Esters", J. Med. Chem. 27, 713-717, (1984).
Alpegiani, M. et al, "On the Preparation of 4-Hydroxymethyl-5-Methyl-1,3-Dioxol-2-One", Synthetic Communications, vol. 22(9), 1277-1282 (1992).
Fischer, H. J. et al, "Darstellung Einiger Dialkylsubstituierter Cycloaddition an Athylen", Tetrahedron Letters No. 17, pp. 1701-1704 (1972).
Stahlke, K.-R. et al, "Zur Photochemie ary-substituierter Vinylencarbonate" Liebigs Ann. Chem. 764, 116-124 (1972).
Cheng Peter T. W.
Poss Michael A.
Sun Chong-Oing
Bristol--Myers Squibb Company
Marquis Melvyn I.
Rodney Burton
LandOfFree
Process for preparing dioxolenone derivatives used for making pr does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Process for preparing dioxolenone derivatives used for making pr, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for preparing dioxolenone derivatives used for making pr will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-444750