Method for producing asymmetric tetrasubstituted carbon...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C546S015000, C548S408000, C562S506000

Reexamination Certificate

active

07928232

ABSTRACT:
The invention provides an industrial method for producing a spiroaminopyrrolidone derivative, which is an intermediate for producing a quinolone antibacterial agent.The invention provides a method for producing a compound represented by formula (2):(wherein n is an integer of 2 to 5; R1represents a (substituted) alkyl group or a (substituted) aryl group; and R2represents a (substituted) alkoxycarbonyl group, a (substituted) aralkyloxycarbonyl group, a (substituted) aliphatic acyl group, or a (substituted) aromatic acyl group), which includes treating a compound represented by formula (1):(wherein n, R1, and R2are the same as defined above; and R3represents a hydrogen atom, a (substituted) alkyl group, or a (substituted) aralkyl group) under a hydrogen gas atmosphere in the presence of a metallic catalyst.

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patent: 7563805 (2009-07-01), Takahashi et al.
patent: 2008/0300403 (2008-12-01), Nishimoto
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Extended European Search Report issued Sep. 27, 2010, in Application No. 06746652.4-2101 / 1882685 PCT/JP2006309996.
Toshihiko Yoshida, et al., “Studies on Quinolone Antibacterials. V.1) Synthesis and Antibacterial Activity of Chiral 5-Amino-7-(-4-substituted-3-amino-1-pyrrolidinyl)-6-fluoro-1,4-dihydro-8-methyl-4-oxoquinoline-3-carboxylic Acid and Derivatives”, Chem. Pharm. Bull., vol. 44, No. 7, (Pharmaceutical Society of Japan, XP002942278, 1996, pp. 1376-1386.

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