Method for producing 3-substituted...

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

Reexamination Certificate

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C546S286000, C546S316000

Reexamination Certificate

active

07414136

ABSTRACT:
To provide a method for producing a 3-substituted 2-chloro-5-fluoro-pyridine or its salt in high yield from a readily available material through a short process under mild reaction conditions using a reagent which is easy for handling and simple in the reaction operation. Namely, a method for producing the following compound (2) or its salt which comprises selectively reducing a chlorine atom at the 6-position of the following compound (1) or its salt, is provided. Further, a method for producing the following compound (4) or its salt which comprises substituting a Z1group of the following compound (2) or its salt obtained by the reduction reaction, by a Z2group, is provided. Here, Z1is —CO2R1, etc., and R1is a hydrogen atom, an alkyl group, an alkenyl group, an aryl group, an aralkyl group or a cycloalkyl group. Z2is a group different from Z1and is —CO2R5, etc., and R5is an alkyl group, an alkenyl group, an aryl group, an aralkyl group or a cycloalkyl group.

REFERENCES:
patent: 5250548 (1993-10-01), Winn et al.
patent: 0254982 (1987-07-01), None
patent: 634413 (1995-01-01), None
patent: WO 98/50362 (1998-11-01), None
Winn et. al., “2-(Alkylamino)nicotinic Acid and Analogs. Potent Angiotensin II Antagonists”, J. Med. Chem. 1993, 36, 2676-2688.
Setliff et al, J. Chemical and Engineering Data, 1972, vol. 17, No. 4, pp. 515-516.

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