Guanidino compounds

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S309000, C514S367000, C514S394000, C514S395000, C514S414000, C514S416000, C514S417000, C544S373000, C546S141000, C548S178000, C548S306100, C548S306400, C548S307100, C548S307400, C548S309400, C548S309700, C548S466000, C548S467000, C548S470000, C548S471000, C548S472000, C548S473000, C548S476000, C548S477000, C548S480000, C548S481000

Reexamination Certificate

active

07456183

ABSTRACT:
Compounds having the general structure I are provided. X and Y are independently selected from the group consisting of CH2, N, NR9, C═O, C═S, S═O, SO2, S, O, (CR6R7)n, C(═O)—(CR6R7)n, and C(═S)—(CR6R7)n, where n is 1, 2, or 3. W is selected from the group consisting of (formula I) and L is selected from the group consisting of N, O, S═O, SO2, C(O), NC(O), NC(S), OC(O), OC(S), C(NR10), C(NOR10), and a covalent bond. Z1, Z2, and Z3are independently selected from the group consisting of substituted carbon and nitrogen. Compounds of formula I are agonists of the melanocortin-4 receptor (“MC-4r2) and therefore may have useful properties for controlling diseases related to MC-4r action in humans, such as obesity and type II diabetes.

REFERENCES:
patent: 3177218 (1965-04-01), Brown
patent: 4128643 (1978-12-01), Merkel et al.
patent: 4287341 (1981-09-01), Hess et al.
patent: 4496571 (1985-01-01), Yellin et al.
patent: 4732916 (1988-03-01), Satoh et al.
patent: 4748165 (1988-05-01), Jones et al.
patent: 4824835 (1989-04-01), Mertens et al.
patent: 4874864 (1989-10-01), Schnur et al.
patent: 4948891 (1990-08-01), Schnur et al.
patent: 4948901 (1990-08-01), Schnur et al.
patent: 5086057 (1992-02-01), Sasagawa et al.
patent: 5124328 (1992-06-01), Fisher et al.
patent: 5352704 (1994-10-01), Okuyama et al.
patent: 5362902 (1994-11-01), Barnish et al.
patent: 5547966 (1996-08-01), Atwal et al.
patent: 5637439 (1997-06-01), Kaneko et al.
patent: 5731408 (1998-03-01), Hadley et al.
patent: 5750573 (1998-05-01), Bianchi et al.
patent: 5866579 (1999-02-01), Wong et al.
patent: 5885985 (1999-03-01), MacDonald et al.
patent: 5889025 (1999-03-01), Lohray et al.
patent: 5952381 (1999-09-01), Chen et al.
patent: 5962530 (1999-10-01), Engel et al.
patent: 6020349 (2000-02-01), Ankersen et al.
patent: 6030985 (2000-02-01), Gentile et al.
patent: 6054556 (2000-04-01), Huby et al.
patent: 6060589 (2000-05-01), Stark et al.
patent: 6127343 (2000-10-01), Ankersen et al.
patent: 6225331 (2001-05-01), Cupps et al.
patent: 6297233 (2001-10-01), Stein et al.
patent: 6391878 (2002-05-01), Cupps et al.
patent: 6638927 (2003-10-01), Renhowe et al.
patent: 6716840 (2004-04-01), Chu et al.
patent: 6960582 (2005-11-01), Boyce
patent: 2004/0024211 (2004-02-01), Boyce et al.
patent: 2005/0038027 (2005-02-01), Boyce et al.
patent: 0 354 553 (1990-02-01), None
patent: 0 343 894 (1992-06-01), None
patent: WO 96/04270 (1996-02-01), None
patent: WO 96/24580 (1996-08-01), None
patent: WO 97/19911 (1997-06-01), None
patent: WO 97/41119 (1997-11-01), None
patent: WO 98/07420 (1998-02-01), None
patent: WO 98/11095 (1998-03-01), None
patent: WO 98/23596 (1998-06-01), None
patent: WO 98/46572 (1998-10-01), None
patent: WO 99/26942 (1999-06-01), None
patent: WO 99/64002 (1999-12-01), None
patent: WO 00/03973 (2000-01-01), None
patent: WO 00/17191 (2000-03-01), None
patent: WO 00/74679 (2000-12-01), None
patent: WO 01/10842 (2001-02-01), None
patent: WO 01/55106 (2001-08-01), None
patent: WO 01/55107 (2001-08-01), None
patent: WO 01/55109 (2001-08-01), None
patent: WO 01/55148 (2001-08-01), None
patent: WO 01/70337 (2001-09-01), None
patent: WO 01/70708 (2001-09-01), None
patent: WO 01/83485 (2001-11-01), None
patent: WO 02/062776 (2002-08-01), None
patent: WO 03/099818 (2003-12-01), None
Wolff (Ed.),Burger's Medicinal Chemistry and Drug Discovery, 5thEdition, vol. 1: Principles and Practice, 1995, pp. 975-977, John Wiley & Sons, Inc.
Banker et al. (Eds.),Modern Pharmaceutics, 3rdEdition, Revised and Expanded, 1996, pp. 451 and 596, Marcel Dekker, Inc.
West,Solid State Chemistry and its Applications, 1988, pp. 358 and 365, John Wiley & Sons, Inc.
Goodfellow et al., “The Melanocortin System and its Role in Obesity and Cachexia,”Current Topics in Medicinal Chemistry, 2003, pp. 855-883, vol. 3, No. 8, Bentham Science Publishers Ltd.
Fisher et al., “Melanocortin-4 receptor: A novel signaling pathwway involved in body weight regulation,”International Journal of Obesity, 1999, pp. 54-58, vol. 23, Suppl. 1, Stockton Press.
Runti et al., “Fusaric Acid Derivatives and Analogues as Possible Antihypertensive Drugs,”Il Farmaco—Ed. Sc., 1981, pp. 260-268, vol. 36, No. 4.
Alexander et al., “(Acyloxy)alkyl Carbamates as Novel Bioreversible Prodrugs for Amines: Increased Permeation through Biological Membranes,”J. Med. Chem., 1988, pp. 318-322, vol. 31, No. 2.
Bell et al., “Efficient synthesis of 1-heterocyclic-3-aminopyrrolidinones,”Tetrahedron Letters, 2000, pp. 1141-1145, vol. 41, Elsevier Science Ltd.
Bhattacharyya et al., “Selective Monoalkylation of Ammonia: A High Throughput Synthesis of Primary Amides,”Synlett, 1999, pp. 1781-1783, No. 11, Thieme Stuttgart, New York.
Brown et al., “Organoboranes for Synthesis. 7. An Improved General Synthesis of Primary Amines From Alkene via Hydroboration-Organoborane Chemistry,”Tetrahedron, 1987, pp. 4071-4078, vol. 43, No. 18, Pergamon Journals Ltd., Great Britain.
Carey et al.,Advanced Organic Chemistry, Part A: Structure and Mechanisms, 3rdEdition, 1990, Table of Contents Only, Plenum Press, New York and London.
Fong et al., “ART (Protein Product of Agouti-Related Transcript) as a Antagonist of MC-3 and MC-4 Receptors,”Biochemical and Biophysical Research Communications, 1997, pp. 629-631, vol. 237, No. 3, Article No. RC977200, Academic Press.
Furniss et al.,Vogel's Textbook of Practical Organic Chemistry, 5thEdition, 1989, Table of Contents Only, Longman Scientific & Technical and John Wiley & Sons, Inc., New York, USA.
Greene,Protective Groups in Organic Synthesis, 1981, Table of Contents Only, John Wiley & Sons, New York, USA.
Hadley et al., “The Proopiomelanocortin System,”Annals New York Academy of Sciences, 1999, pp. 1-21, vol. 885.
http://www.idealibrary.com/links.doi/10.1006/bbrc.1997, Fong et al., “ART (Protein Product of Agouti-Related Transcript) as an Antagonist of MC-3 and MC-4 Receptors,”Biochemical and Biophysical Research Communications, Aug. 28, 1997, pp. 629-631, vol. 237, No. 3, ISSN:0006-291X, EISSN:1090-2104, Abstract Only.
http://www.sciencemag.org/...ar=2001&hits=10&sendit.x=36&sendit.y, Ollman et al., “Antagonism of Central Melanocortin Receptors in Vitro and in Vivo by Agouti-Related Protein,”Science, Oct. 3, 1997, pp. 135-138, vol. 278.
Huszar et al., “Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in Mice,”Cell, Jan. 10, 1997, pp. 131-141, vol. 38, Cell Press.
Julia et al., “Amidines et guanidines apparentées á la congocidine,”Bulletin De La Société Chimique De France, 1968, pp. 376-382, No. 1.
Kiefer et al., “Mutations in the Carboxyl Terminus of the Agouti Protein Decrease Agouti Inhibition of Ligand Binding to the Melanocortin Receptors,”Biochemistry, 1997, pp. 2084-2090, vol. 36, American Chemical Society.
LaRock,Comprehensive Organic Transformations, A Guide to Functional Group Preparations, 1989, Table of Contents Only, VCH Publishers, Inc., USA.
Lu et al., “Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor,”Nature, Oct. 27, 1994, pp. 799-802, vol. 371.
March,Advanced Organic Chemistry, Reactions, Mechanisms, and Structure, 3rdEdition, 1985, Table of Contents Only, John Wiley & Sons.
Mickelson et al., “Asymmetric Synthesis of 2,6-Methylated Piperazines,”J. Org. Chem., 1995, pp. 4177-4183, vol. 60, No. 13, American Chemical Society.
Mountjoy et al., “The Cloning of a Family of Genes that Encode the Melanocortin Receptors,”Science, Aug. 28, 1992, pp. 1248-1251, vol. 257.
Nevy et al., “Transition State Imbalance in the Deprotonation of Substituted 2-Tetralones by Hydroxide Ion,”J. Am. Chem. Soc., 1997, pp. 12722-12726, vol. 119, No. 52, American Chemical Society.
Ollmann et al., “Antagonism of Central Melanocortin Receptors in Vitro

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