Pyridyl substituted heterocycles useful for treating or...

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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C514S333000, C514S340000, C514S342000, C546S255000, C546S256000, C546S268100, C546S269700

Reexamination Certificate

active

10646348

ABSTRACT:
The present invention relates to pyridyl substituted heterocycles and hydro isomers thereof and pharmaceutical compositions thereof that inhibit replication and/or proliferation of HCV virus. The present invention also relates to the use of the pyridyl heterocycles and hydro isomers thereof and/or pharmaceutical compositions comprising the compounds to treat or prevent HCV infections.

REFERENCES:
patent: 2852503 (1958-09-01), Edward et al.
patent: 3257203 (1966-06-01), Klupfel et al.
patent: 3335149 (1967-08-01), Preston
patent: 3910942 (1975-10-01), Narayanan et al.
patent: 3964896 (1976-06-01), Neidermyer et al.
patent: 4752324 (1988-06-01), Thomas et al.
patent: 5151441 (1992-09-01), Mueller et al.
patent: 5256666 (1993-10-01), Mueller et al.
patent: 5463071 (1995-10-01), Himmelsbach et al.
patent: 5814627 (1998-09-01), Schwab et al.
patent: 6355669 (2002-03-01), Yamauchi et al.
patent: 2002/0035156 (2002-03-01), Roniker et al.
patent: 2002/0049213 (2002-04-01), Weidner-Wells et al.
patent: 559 195 (1975-02-01), None
patent: 21 37 719 (1973-02-01), None
patent: 27 21 955 (1978-11-01), None
patent: 100 32 874 (2002-01-01), None
patent: 101 48 598 (2002-10-01), None
patent: 563686 (1993-03-01), None
patent: 0 776 894 (1997-06-01), None
patent: 92/7992 (1999-07-01), None
patent: 1 180 518 (2002-02-01), None
patent: 1 348 706 (2003-10-01), None
patent: 1 459 375 (1966-04-01), None
patent: 04124178 (1992-04-01), None
patent: WO 93/17671 (1993-09-01), None
patent: WO 94/17059 (1994-06-01), None
patent: WO 95/24397 (1995-09-01), None
patent: WO 98/17652 (1998-04-01), None
patent: WO 98/47509 (1998-10-01), None
patent: WO 99/04390 (1999-01-01), None
patent: WO 99/20309 (1999-04-01), None
patent: WO 02/20436 (2000-03-01), None
patent: WO 00/40242 (2000-07-01), None
patent: WO 00/45799 (2000-08-01), None
patent: WO 00/78726 (2000-12-01), None
patent: WO 01/74811 (2001-10-01), None
patent: WO 01/78648 (2001-10-01), None
patent: WO 02/46186 (2002-06-01), None
patent: WO 02/055025 (2002-07-01), None
patent: WO 03/029210 (2003-04-01), None
patent: WO 03/040112 (2003-05-01), None
patent: WO 04/018463 (2004-03-01), None
patent: WO 04/103366 (2004-12-01), None
Roth et al., “Zur Kondensation von Chalkonoxyden mit Hydroxylamin”,Arch. Pharm., vol. 94, pp. 769-774, 1961.
Samula, “Oksymowanic Azachalkonow”,Roczniki Chemll, Ann. Soc. Chim. Polonorum, vol. 45, pp. 2063, 1971.
Samula, “Cyclization of Azachalcones and β-Hydroxyketones Oximes”,Roczniki Chemll, Ann. soc. Chim, Polonorum, vol. 48, pp. 959-964, 1974.
Howe, et al., “Nitrile Oxide Cycloaddition Routes to 2-(Isoxazoly)-benzoates and 2-(1,2,4-Oxadiazol-3-yl)benzoates”,Heterocycl. Chem., vol. 19, No. 4, pp. 721-726, 1982.
Belgodere et al., “Studies on Isomeric Pyridylisoxazoles”,Heterocycles, vol. 20, No. 3, pp. 501-504, 1983.
Batori et al., “Photoinduced Ring Transformation of Pyrido[1,2-b]pyridazinium-4-olate”,Tetrehedron, vol. 50, No. 16, pp. 4699-4708, 1994.
Kanbara et al., “Preparation of Soluble and Fluorescent Poly(arylene)s by 1,3-Dipolar Polycycloaddition and Properties of the Polymers”,Polymer Bulletin, vol. 36, pp. 673-679, 1996.
Ku et al., “Use of Iodoacetylene as a Dipolarphile in the Synthesis of 5-Iodoisoxazole Derivatives”,Organic Letters, vol. 3, No. 26, pp. 4185-4187, 2001.
Maybridge, plc, Trevillett, Tintagel, Catalogue No. RF01972, Cornwall PL34 OHW, England.
Maybridge, plc, Trevillett, Tintagel, Catalog No. RF01996, Cornwall PL34 OHW, England.
Gatta et al, “Synthesis of [1,2,4]Triazoloquinazoline and [1,2,4]Triazolo-1,4-benzodiazepine derivatives”,J. Heterocyclic. Chem., vol. 30, pp. 11-16, 1993.
International Search Report.
Gatta et al. Synthesis of [1,2,4] Triazoloquinazoline and [1,2,4] Triazolo- 1,4-benzodiazepine derivatives. Journal of Heterocyclic Chemistry. (1993), vol. 30, pp. 11-16.
Database Chemcats Online! 1999m XP-002310049, Databased accession No. RN 247059-16-1.
Maybridge Hts, Order No. BTB 09742; RN 247059-16-1 Maybridge PLC, Trevillett, Tintagel, Cornwall, PL340HW, UK, Jan. 8, 2004 XP002297442.
STN File CA, Abstract 135:46129 & V.M. Barot et al, Asian Journal of Chemistry (2001), 13(1), pp. 341-343.
STN File CA, Abstract 132:265141 & S.V. Damle et al, Indian Journal of Heterocyclic Chemistry (1999), 9(2), pp. 81-86.
STN File CA, Abstract 132:180505 & V.R. Naik et al, Asian Journal of Chemistry (2000), 12(1), pp. 305-307.
STN File CA, Abstract 129:216539 & S.M. Naik et al, Oriental Journal of Chemistry (1998), 14(1), pp. 167-168.
STN File CA, Abstract 126:74789 & M. Shah et al, Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (1996), 35B(12), pp. 1282-1286.
STN File CA, Abstract 122:81186 & S.R. Modi et al, Oriental Journal of Chemistry (1994), 10(1), pp. 85-86.
STN File CA, Abstract 118:191597 & T. Bandiera et al, Journal of Heterocyclic Chemistry (1992), 29(6), pp. 1423-1428.

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