Intermediate of 6-substituted 1-methyl-1-H-benzimidazole...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters

Reexamination Certificate

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C564S280000

Reexamination Certificate

active

07816552

ABSTRACT:
A method for preparing a compound having the following formula (I)by reducing a nitro group of the following formula (III)followed by carrying out an intramolecular dehydration condensation, wherein R2is hydrogen, alkyl, cycloalkyl, phenyl or a 5- or 6-membered heterocyclic, and X is oxygen, sulfur or nitrogen.

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Junya Ohmori et al., “Novel AMPA Receptor Antagonists: Synthesis and Structure-Activity Relationships of 1-Hydroxy-7-(1H-imidazol-1-yl)-6-nitro-2,3(1H,4H)—quinoxalinedione and Related Compounds,”J. Med. Chem., vol. 39, pp. 3971-3979, (1996), USA.
English-language International Preliminary Report on Patentability and Written Opinion of the International Searching Aughority, dated Apr. 12, 2007 for International application PCT/JP2005/017573 filed Sep. 28, 2005; Applicants: Sankyo Company Limited et al.
Junya Ohmori et al., “Novel AMPA Receptor Antagonists: Synthesis and Structure-Activity Relationships of 1-Hydroxy-7-(1H-imidazol-1-yl)-6-nitro-2,3) (1H, 4H)—quinoxalinedione and Related Compounds”,Journal of Medicinal Chemistry, (1996), 39, 3971-3979.
Supplementary European Search Report dated Oct. 24, 2008 in European Application EP 05785694.

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