Heterocyclic 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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Details

C514S345000, C514S340000, C514S344000, C514S895000, C546S290000, C546S296000, C546S300000, C546S302000

Reexamination Certificate

active

07629365

ABSTRACT:
3-Chloro-6-(hydroxymethyl)-2-methyl-5-[4-({4-[(trifluoromethyl)oxy]phenyl}oxy)phenyl]-4(1H)-pyridinone, having the following formula:is described along with its pharmaceutically acceptable salts, processes for its preparation, pharmaceutical formulations thereof and its uses in treatment of certain parasitic infections such as malaria.

REFERENCES:
patent: 5403934 (1995-04-01), Batchelor et al.
patent: 0447164 (1991-09-01), None
patent: WO-9113873 (1991-09-01), None
Nitta et al, Mo(CO)n induced N-O bond cleavage of isoxazoles a convenient route to pyridin-4(1H) ones, Heterocycles, vol. 38, No. 4 1994.
Patani et al , bioisosterism: A rational Approach in drug design, Chemical reviews, 1996, vol. 96, pp. 3147-3176.

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