Process for preparation of amidine derivatives

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

Reexamination Certificate

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C546S089000, C546S153000, C546S159000, C546S160000

Reexamination Certificate

active

06987187

ABSTRACT:
A process for producing amidine derivatives represented by the following reaction scheme, characterized in that the reactions of steps 1 and 3 are conducted in acetonitrile and the reaction of step 2 is conducted in acetone.

REFERENCES:
patent: 5461062 (1995-10-01), Takada et al.
patent: 556008 (1993-08-01), None
patent: 1 270 578 (2003-01-01), None
patent: 0157443 (1992-05-01), None
patent: 01/74821 (2001-10-01), None
Volovenko et al, Chem. Abs. vol. 117 No. 233799, “Synthesis and biological activity of alpha sub. 2-pyridylacetonitirl;es” (1992) (Best Available).
M. Adachi et al., “Intermolecular transfer of an alkenyl group in enamines: application to synthesis of [b]-fused pyridins”, Tetrahedron Letters, 1996, vol. 37, No. 49, pp. 8871-8874.
M. Dolezal et al., “Synthesis and antimycobacterial, antigungal, and photosynthesis-inhibiting evaluation of some anilides of substituted pyrazine-2-carboxylic acids”, Chemical Papers, 2000, vol. 54, No. 4, pp. 245-248.
M. Adachi et al., “Intermolecular transfer of an alkenyl group in enamines: application to synthesis of [b]-fused pyridins”, Tetrahedron Letters, 1996, vol. 37, No. 49, pp. 8871-8874.
M. Dolezal et al., “Synthesis and antimycobacterial, antigungal, and photosynthesis-inhibiting evaluation of some anilides of substituted pyrazine-2-carboxylic acids”, Chemical Papers, 2000, vol. 54, No. 4, pp. 245-248.

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