Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters
Patent
1995-07-14
1996-07-16
Geist, Gary
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acid esters
C07C22924
Patent
active
055368697
ABSTRACT:
The present invention relates to a novel process for the preparation of ethyl 3S-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentyno ate and pharmaceutically acceptable acid addition salt thereof which comprises treating (trimethylsilyl)acetylene sequentially with n-butyllithium and 4-formylmorpholine followed by acid hydrolysis to give 3-(trimethylsilyl)-2-propynal; treating 3-(trimethylsilyl)-2-propynal with lithium bis(trimethylsilyl)amide to give in situ N,3-bis(trimethylsilyl)-2-propyn-1-imine; condensation of N,3-bis(trimethylsilyl)-2-propyn-1-imine with lithium t-butyl acetate to give (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate; treating (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate- with p-toluenesulfonic acid to give (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate, mono p-toluenesulfonic acid salt, treatment of resulting salt with ethanol in the presence of p-toluenesulfonic acid to give (.+-.)ethyl 3-amino-5-(trimethylsilyl)-4-pentynoate; desilylation of (.+-.)ethyl 3-amino-5-(trimethylsilyl)-4-pentynoate to give in situ (.+-.)ethyl 3-amino-4-pentynoate; resolution of (.+-.)ethyl 3-amino-4-pentynoate using (R)-(-)-mandelic acid and treatment of the resolved product with gaseous hydrochloric acid to give ethyl 3S-amino-4-pentynoate, monohydrochloride; coupling the ethyl 3S-amino-4-pentynoate, monohydrochloride to 4-[[4-(aminoiminomethyl)phenyl]amino]-4-oxobutanoic acid, monohydrochloride in the presence of isobutyl chloroformate and N-methylmorpholine to give ethyl 3S-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentyno ate, monohydrochloride.
REFERENCES:
patent: 5239113 (1993-08-01), Bovy et al.
patent: 5344957 (1994-09-01), Bovy et al.
D. Hua et al. "Synthesis of 4-Substituted 2-Azetidinones", Tetrahedron Letters, vol. 26, No. 5, pp. 547-550 (1985), Great Britain.
T. Kametani "Synthesis of Carbapenem Antibiotics", Heterocycles, vol. 17, pp. 463-506, (1982), Tokyo, Japan.
D. Cole "Recent Stereoselective Synthetic Approaches to .beta.-Amino Acids", Tetrahedron vol. 50, No. 32, pp. 9517-9582 (1994), Great Britain.
J. Rico, et al. "A Highly Stereoselective Michael Addition To An .alpha.,.beta.-Unsaturated Ester As The Crucial Step In the Synthesis Of A Novel .beta.-Amino Acid-Containing Fibrinogen Receptor Antagonist", J. Org. Chem, 58, pp. 7948-7951 (1993), Washington, D.C., U.S.A.
E. Juaristi, et al. "Enantioselective Synthesis of .beta.-Amino Acids", Aldrichimica Acta, vol. 27, No. 1 (1994), Milwaukee, WI, U.S.A.
K. Hattori, et al. "Highly Selective And Operationally Simple Synthesis of Enantiomerically Pure .beta.-Amino Esters Via Double Stereodifferentiation", J. Am. Chem. Soc., 115, pp. 1151-1152 (1993), Washington, D.C., U.S.A.
G. Iwasaki, et al. "Further Studies On the Stereochemistry Of Metal Enolate-Imine Condensation Reactions", Tetrahedron Let., vol. 28, No. 28, pp. 3257-3260 (1987), Great Britain.
K. Hattori, et al. "A Novel Stereocontrolled Synthesis of 3-(1'-Hydroxyethyl)-2-Azetidinone", Synlett (3) pp. 239-240 (1993), Stuttgart, Germany.
Babiak Kevin A.
Babu Srinivasan
Behling James R.
Boys Mark L.
Cain-Janicki Kimberly J.
Conrad, III Joseph M.
G. D. Searle & Co.
Geist Gary
Serauskas Joy Ann
Williams Roger A.
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