Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2011-03-22
2011-03-22
Chandrakumar, Nizal S (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C549S356000
Reexamination Certificate
active
07910751
ABSTRACT:
A compound represented by formula (I′):(wherein m, n, and p each represent 0 to 2; q represents 0 or 1; R1represents halogen, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, a sulfamoyl group, a CN group, an NO2group, or the like; R2represents halogen, amino, a hydrocarbon group, an aromatic heterocyclic group, or an oxo group; X1represents O, —NR3—, or —S(O)r-; X2represents a methylene group, O, —NR3—, or —S(O)r-; Q′ represents a heteroaryl group, a heteroarylalkyl group, a substituted aryl group, or an aralkyl group; Cycle moiety represents an aryl ring or a heteroaryl ring; and the wavy line represents an E-isomer or a Z-isomer), a salt of the compound, or a solvate of the compound or the salt. A pharmaceutical composition and a transient receptor potential type I (TRPV1) receptor antagonist each contain, as an active ingredient, at least one of the compound, a salt of the compound, and a solvate of the compound or the salt.
REFERENCES:
patent: 4977166 (1990-12-01), Hardy et al.
patent: 5710150 (1998-01-01), Taniguchi et al.
patent: 6120964 (2000-09-01), Wilson et al.
patent: 6340678 (2002-01-01), Matsuhisa et al.
patent: 2004/0038969 (2004-02-01), Doherty et al.
patent: 2004/0204477 (2004-10-01), Moll et al.
patent: 2005/0004103 (2005-01-01), Koshio et al.
patent: 2006/0035882 (2006-02-01), Koga et al.
patent: 2007/0167444 (2007-07-01), Kuramochi et al.
patent: 2008/0287428 (2008-11-01), Uchida et al.
patent: 2010/0016285 (2010-01-01), Uchida et al.
patent: 0 411 751 (1991-02-01), None
patent: 1 109 071 (2001-06-01), None
patent: 1 619 185 (2006-01-01), None
patent: 1 829 864 (2007-09-01), None
patent: A-4-178381 (1992-06-01), None
patent: 05-339223 (1993-12-01), None
patent: A-9-221475 (1997-08-01), None
patent: A-2001-213870 (2001-08-01), None
patent: A-2005-187449 (2005-07-01), None
patent: WO 94/26692 (1994-11-01), None
patent: WO 95-06035 (1995-03-01), None
patent: WO 97/12870 (1997-04-01), None
patent: WO 98/07704 (1998-02-01), None
patent: WO 98/39325 (1998-09-01), None
patent: WO 98/42673 (1998-10-01), None
patent: WO 03/042181 (2003-05-01), None
patent: WO 03/049702 (2003-06-01), None
patent: WO 2004/052846 (2004-06-01), None
patent: WO 2004/056774 (2004-07-01), None
patent: WO 2004/069792 (2004-08-01), None
patent: WO 2004/100865 (2004-11-01), None
patent: WO 2004/110986 (2004-12-01), None
patent: WO 2005/016922 (2005-02-01), None
patent: WO 2005/030766 (2005-04-01), None
patent: WO 2005/040100 (2005-05-01), None
patent: WO 2005/040119 (2005-05-01), None
patent: WO 2005/040121 (2005-05-01), None
patent: WO 2005/046683 (2005-05-01), None
patent: WO 2005/070885 (2005-08-01), None
patent: WO 2005/095329 (2005-10-01), None
patent: WO 2006/006741 (2006-01-01), None
patent: WO 2006/038871 (2006-04-01), None
patent: WO 2006/058338 (2006-06-01), None
patent: WO 2006/064075 (2006-06-01), None
patent: WO 2007/010383 (2007-01-01), None
patent: WO 2008/091021 (2008-07-01), None
patent: WO 2010/010933 (2010-01-01), None
patent: WO 2010/010934 (2010-01-01), None
patent: WO 2010/010935 (2010-01-01), None
patent: WO 2010/038803 (2010-04-01), None
Dorwald F. A. Side Reactions in Organic Synthesis, 2005, Wiley: VCH, Weinheim p. IX of Preface p. 1-15.
West, Solid State Chemistry and its applications, John Wiley & Sons, 1984, p. 358.
Di Fabio et al., “Benzoazepine derivative as potent antagonists of the glycine binding site associated to the NMDA receptor,”Il Farmaco, vol. 58, No. 9, 2003, pp. 723-738.
Messeri et al., “Efficient synthesis of novel benzo-[e]-[1,4]-diazepine derivatives,”Tetrahedron Letters, vol. 42, No. 18, 2001, pp. 3227-3230.
Matsuhisa et al., “Nonpeptide Arginine Vasopressin Antagonists for Both V1Aand V2Receptors: Synthesis and Pharmacological Properties of 4′-[5-(Substituted Methylidene)-2,3,4,5-tetrahydro-1H-1-benzoazepine-1-carbonyl]benzanilide and 4′-[5-(Substituted Methyl)-2,3-dihydro-1H-1benzoazepine-1-carbonyl]benzanilide Derivatives,”Chemical Pharmaceutical Bulletin, vol. 47, No. 3, 1999, pp. 329-339.
Tacconi, “Reazione di Schmidt su ossindolil e ossindolidenchetoni,”Gazzetta Chimica Italiana, vol. 98, No. 3, 1968, pp. 344-357 (with abstract).
Barberan et al., “Synthesis ofE- andZ-substituted methylene-3,4-dihydro-2H-1 benzopyrans by region- and stereocontrolled palladium-catalyzed intramolecular cyclization,”Tetrahedron Letters, vol. 42, No. 14, 2001.
Canoira et al., “Synthesis of Oxindole Derivatives fromN-Alkenyl-o-Chloranilides with Zero-Valent Nickel Complex,”Journal of Heterocyclic Chemistry, vol. 22, No. 6, 1985, pp. 1511-1518.
R. Di Fabio, “Enantiomerically Pure Tetrahydroquinoline Derivatives as In Vivo Potent Antagonists of the Glycine Binding Site Associated to the NMDA Receptor”,Bioorganic&Medicinal Chemistry Letters, vol. 13, No. 21, pp. 3863-3866, Nov. 2003.
Supplementary European Search Report dated Sep. 10, 2009.
Bannon et al., “Involvement of TRPV1 in the Regulation of Body Temprature in Rats and Mice”, Society for Neuroscience Abstract 30:890.24, pp. 1-2, 2004.
Gavva et al., “The Vanilloid Receptor TRPV1 is Tonically ActivatedIn Vitro and Involved in Body Temperature Regulation”, The Journal of Neuroscience, vol. 27, No. 13, pp. 3366-3374, Mar. 28, 2007.
Gavva, “Body-Temperature Maintenance as the Predominant Function of The Vanilloid Receptor TRPV1”, Trends in Pharmacological Science, vol. 29, No. 11, pp. 550-557, Sep. 19, 2008.
Swanson et al., “Identification and Biological Evaluation of 4(3-Trifluoromethylpyridin-2-yl)peperazine-1-carboxylic Acid (5-Trifluoromethylpyridin-2-yl)amide, a High Affinity TRPV1 (VR1) Vanilloid Receptor Antagonist”, J. Med. Chem., vol. 48, pp. 1857-1872, 2005.
Akada Yasushige
Amano Ken-ichi
Hotta Daido
Kamino Tomoyuki
Kosuga Naoto
Chandrakumar Nizal S
Mochida Pharmaceutical Co. Ltd.
Oliff & Berridg,e PLC
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