Bicyclic imidazo-5-yl-amine derivatives

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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Details

C514S393000, C548S262400, C548S303100

Reexamination Certificate

active

06936631

ABSTRACT:
A novel bicyclic imidazo-5-yl-amine derivative of Formula I,wherein X denotes CR5, N or S, and Y in the case where X denotes S, denotes CR6or N and in all other cases denotes N, and methods for preparation thereof are disclosed. Also disclosed are methods for treating pain using the compound of Formula I, and pharmaceutical compositions comprising the compound of Formula I.

REFERENCES:
patent: 6657064 (2003-12-01), Gerlach et al.
patent: 0518033 (1992-12-01), None
Lantos et. al., “Novel Synthesis of Fused-Imidazoles III. Simplified Construction of the Imidazo[2,1-b]Thiazoline System”, Heterocycles, vol. 24, No. 4, 1996.
Ca 81:105382b, Cyclization of w-chLoro-w-acyLamido acetophenones, Drach et al., vol. 81, 1974.
Ca 58:2443e, “Bicyclic heterocyclic componds with a common N atom amnoimidazo [2,1-b]tioazoles”, Pyl et. al. See RN 95315-23-4 and 95315-26-7.
Hugues Bienayme, et al. “A New Heterocyclic Multicomponent Reaction for the Combinatorial Synthesis of Fused 3-Aminoimidazoles” Angew. Chem. Int. Ed. vol. 37, No. 16, 1998, pp. 2234-2237.
Katrin Groebke, et al., “Synthesis of Imidazo [1,2-a] annulated Pyridines, Pyrazines and Pyrimidines by a Novel Three-Component Condensation” Synlett, Jun. 1998.
Hugues Bienayme, et al., “A New Heterocyclic Multicomponent Reaction for the Combinatorial Synthesis of Fused 3-Aminoimidazoles” Angew. Chem. Int. Ed. vol. 37, No. 16, 1998.

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