Timothy L. Stuk - Lindenhurst IL Michael S. Allen - Silver Lake WI Anthony R. Haight - Mundelein IL Francis A. Kerdesky - Grayslake IL Denton C. Langridge - Wildwood IL M. Robert Leanna - Grayslake IL Linda M. Lijewski - Milwaukee WI Laura Melcher - Deerfield IL Howard E. Morton - Gurnee IL Daniel W. Norbeck - Crystal Lake IL Daniel S. Reno - Kenosha WI Timothy A. Robbins - Gurnee IL Hing L. Sham - Mundelein IL Thomas J. Sowin - Grayslake IL Chen Zhao - Gurnee IL David Scarpetti - Baltimore MD
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
C07C25178 C07C22114 C07C20944
US Classification:
546 99
Abstract:
A substantially pure compound of formula: ##STR1## wherein R. sub. 6 and R. sub. 7 are independently selected from ##STR2## wherein R. sub. a and R. sub. b are independently selected from hydrogen, loweralkyl and phenyl and R. sub. c, R. sub. d and R. sub. e are independently selected from hydrogen, loweralkyl, trifluoromethyl, alkoxy, halo and phenyl; and ##STR3## wherein the naphthyl ring is unsubstituted or substituted with one, two or three substitutents independently selected from loweralkyl, trifluoromethyl, alkoxy and halo; or R. sub. 6 is as defined above and R. sub. 7 is R. sub. 7a OC(O)-- wherein R. sub. 7a is loweralkyl; or R. sub. 6 and R. sub. 7 taken together with the nitrogen atom to which they are bonded are ##STR4## wherein R. sub. f, R. sub. g, R. sub. h and R. sub. l are independently selected from hydrogen, loweralkyl, alkoxy, halogen and trifluoromethyl; and R. sub. g is hydrogen, loweralkyl or benzyl; or an acid addition salt thereof.
Process For The Preparation Of A Substituted 2.5-Diamino-3-Hydroxyhexane
Timothy L. Stuk - Lindenhurst IL Michael S. Allen - Silver Lake WI Anthony R. Haight - Mundelein IL Francis A. Kerdesky - Grayslake IL Denton C. Langridge - Wildwood IL M. Robert Leanna - Grayslake IL Linda M. Lijewski - Milwaukee WI Laura Melcher - Deerfield IL Howard E. Morton - Gurnee IL Daniel W. Norbeck - Crystal Lake IL Daniel S. Reno - Kenosha WI Timothy A. Robbins - Gurnee IL Hing L. Sham - Mundelein IL Thomas J. Sowin - Grayslake IL Chen Zhao - Gurnee IL David Scarpetti - Baltimore MD
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
C07C26100 C07C23300 C07D20904
US Classification:
560 24
Abstract:
Intermediates and processes are disclosed which are useful for the preparation of a substantially pure compound of the formula: ##STR1## wherein R. sub. 6 and R. sub. 7 are each hydrogen or R. sub. 6 and R. sub. 7 are independently selected from ##STR2## wherein R. sub. a and R. sub. b are independently selected from hydrogen, loweralkyl and phenyl and R. sub. c, R. sub. d and R. sub. e are independently selected from hydrogen, loweralkyl, trifluoromethyl, alkoxy, halo and phenyl; and ##STR3## wherein the naphthyl ring is unsubstituted or substituted with one, two or three substitutents independently selected from loweralkyl, trifluoromethyl, alkoxy and halo; or R. sub. 6 is as defined above and R. sub. 7 is R. sub. 7a OC(O)-- wherein R. sub. 7a is loweralkyl or benzyl; or R. sub. 6 and R. sub.
Process For The Preparation Of A Substituted 2.5-Diamono-3-Hydroxy-Hexane
Timothy L. Stuk - Lindenhurst IL Anthony R. Haight - Mundelein IL Francis A. J. Kerdesky - Grayslake IL M. Robert Leanna - Grayslake IL Howard E. Morton - Gurnee IL Timothy A. Robbins - Gurnee IL David Scarpetti - Baltimore MD
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
C07C26100 C07C23300
US Classification:
560 27
Abstract:
Intermediates and processes are disclosed which are useful for the preparation of a substantially pure compound of the formula: ##STR1## wherein R. sub. 6 and R. sub. 7 are each hydrogen or R. sub. 6 and R. sub. 7 are independently selected from ##STR2## wherein R. sub. a and R. sub. b are independently selected from hydrogen, loweralkyl and phenyl and R. sub. c, R. sub. d and R. sub. e are independently selected from hydrogen, loweralkyl, trifluoromethyl, alkoxy, halo and phenyl; and ##STR3## wherein the naphthyl ring is unsubstituted or substituted with one, two or three substitutents independently selected from loweralkyl, trifluoromethyl, alkoxy and halo; or R. sub. 6 is as defined above and R. sub. 7 is R. sub. 7a OC(O)-- wherein R. sub.
Guilford Pharmaceuticals 1998 - 2000
Senior Scientist
Cas 1998 - 2000
Scientific Information Analyst
Fda 1994 - 1998
Chemist, Center For Drug Evaluation and Research
Abbott 1991 - 1994
Chemist, Process Reasearch and Development
Education:
Purdue University 1986 - 1991
Doctorates, Doctor of Philosophy, Organic Chemistry
University of Massachusetts Boston 1981 - 1986
Bachelors, Bachelor of Science, Chemistry
Skills:
Intellectual Property Gmp Patent Searching Data Curation Quality Assurance Searching All Files on Stn Active Pharmaceutical Ingredients Patent Applications Organic Chemistry Analytical Chemistry Hp Quality Center Jira Technology Transfer
2000 to 2000 Scientific Information AnalystGuilford Pharmaceuticals Baltimore, MD 1998 to 2000 Senior ScientistFood and Drug Administration Rockville, MD 1994 to 1998 Chemist in Center of Drug Evaluation and ResearchAbbott Laboratories North Chicago, IL 1991 to 1994 Process Research and Development Chemist
Education:
Purdue University 1991 Ph.D. in ChemistryUniversity of Massachusetts/Boston Boston, MA 1986 B.S. in Chemistry