Isoxazole derivatives and process for producing the same

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

Reexamination Certificate

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Reexamination Certificate

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07453001

ABSTRACT:
The present invention provides isoxazole derivatives represented by the following formula (I):(wherein R1represents a hydrogen atom, C1-C20hydrocarbon group or —C(═O)OR1a(wherein R1arepresents a C1-C10alkyl group, etc.); R2and R3represent a hydrogen atom, halogen atom, hydroxy group, C1-C20alkyl group or C6-C20aryl group, etc.; R4represents a hydrogen atom, halogen atom, hydroxy group, cyano group, nitro group, amino group, C1-C20hydrocarbon group, C1-C10alkoxy group, C1-C10acyl group, 5- to 7-membered heterocyclic group, etc.; R5represents a hydrogen atom, halogen atom, hydroxy group, optionally substituted C1-C20hydrocarbon group, C1-C20alkoxy group, 5- to 7-membered heterocyclic group, etc.; and, n represents 0, 1, 2, 3 or 4), and a process of producing the same. The compounds are useful as intermediates for synthesis of pharmaceutical compounds, agricultural chemicals, dye compounds, etc. having the isoxazole skeleton.

REFERENCES:
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Easton, C.J. et al., Reversal of Regiochemistry in the Synthesis of Isoxazoles by Nitrile Oxide Cycloadditions, Tetrahedron Letters, 1994, vol. 35, No. 21, pp. 3589 to 3592, formula 3a, scheme 1.
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Supplementary European Search Report for EP 02 79 2015 completed Oct. 19, 2005.
Shutske, G. M. “A Novel Synthesis of the Isoxazolo [5, 4, 3-kl] acridine Ring System.” J. Heterocyclic Chem. vol. 27, No. 6, pp. 1617-1621, Formula 1 (1990).
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