Plant protecting and regulating compositions – Plant growth regulating compositions – Organic active compound containing
Reexamination Certificate
2007-07-10
2007-07-10
Saeed, Kamal A. (Department: 1626)
Plant protecting and regulating compositions
Plant growth regulating compositions
Organic active compound containing
C514S406000, C548S374100
Reexamination Certificate
active
10540036
ABSTRACT:
A fungicidally active compound of formula (I): where Het is a substituted 5- or 6-membered heterocyclic ring; R1is hydrogen, formyl, CO—C1-4alkyl, COO—C1-4alkyl, C1-4alkoxy(C1-4)alkylene, CO—C1-4alkylenoxy(C1-4)alkyl, propargyl or allenyl; R2, R3, R4and R5are each, independently, hydrogen, halogen, methyl or CF3; each R6is, independently, halogen, methyl or CF3; R7is (Z)mC═C(Y1), (Z)mC(Y1)═C(Y2)(Y3) or tri(C1-4)alkylsilyl; X is O or S; Y1, Y2and Y3are each, independently, hydrogen, halogen, C1-6alkyl [optionally substituted by one or more substituents each independently selected from halogen, hydroxy, C1-4alkoxy, C1-4haloalkoxy, C1-4alkylthio, C1-4haloalkylthio, C1-4alkylamino, di(C1-4)alkylamino, C1-4alkoxycarbonyl, C1-4alkylcarbonyloxy and tri(C1-4)alkylsilyl], C2-4alkenyl [optionally substituted by one or more substituents each independently selected from halogen], C2-4alkynyl [optionally substituted by one or more substituents each independently selected from halogen], C3-7cycloalkyl [optionally substituted by one or more substituents each independently selected from halogen, C1-4alkyl and C1-4haloalkyl] or tri(C1-4)alkylsilyl; Z is C1-4alkylene [optionally substituted by one or more substituents each independently selected from hydroxy, cyano, C1-4alkoxy, halogen, C1-4haloalkyl, C1-4haloalkoxy, C1-4alkylthio, COOH and COO—C1-4alkyl]; m is 0 or 1; and n is 0, 1 or 2; the invention also relates to novel intermediates used in the preparation of these compounds, to agrochemical compositions which comprise at least one of the novel compounds as active ingredient and to the use of the active ingredients or compositions in agriculture or horticulture for controlling or preventing infestation of plants by phytopathogenic microorganisms, preferably fungi
REFERENCES:
patent: 3859338 (1975-01-01), Engel et al.
patent: 3928364 (1975-12-01), Seeger et al.
patent: 4016214 (1977-04-01), Douglas et al.
patent: 4036989 (1977-07-01), Armitage et al.
patent: 6503932 (2003-01-01), Eicken
patent: 6515000 (2003-02-01), Eicken
patent: 7098227 (2006-08-01), Dunkel et al.
patent: 2004/0029930 (2004-02-01), Eicken
patent: 2004/0044060 (2004-03-01), Muller
patent: 2004/0077692 (2004-04-01), Eicken
patent: 2005/0124815 (2005-06-01), Elbe et al.
patent: 2006/0116414 (2006-06-01), Dunkel et al.
patent: 2006/0148886 (2006-07-01), Dunkel et al.
patent: 2205732 (1973-08-01), None
patent: 2205732 (1976-05-01), None
patent: 10204390 (2003-08-01), None
patent: 10204391 (2003-08-01), None
patent: 10215292 (2003-08-01), None
patent: 10218231 (2003-11-01), None
patent: 2001302605 (2001-10-01), None
patent: 0208197 (2002-01-01), None
patent: WO 0208195 (2002-01-01), None
patent: 2004045282 (2004-06-01), None
D.C. Naae et al.: “The solid-gas chlorination and bromination of a fluorinated of a fluorinated olefin.” Tetrahedron Letters, vol. 32, 1976, pp. 2761-2764, p. 2762, table.
J.L. Chanal, et al., “Comparison of the Metabolism and Pharmacokinetics of Metbufen and Itanoxone and their Analogues in Rats.” Arzneimittel Forschung, vol. 38, No. 10, 1988, pp. 1454-1460, p. 1456, compound la.
D.G. Naae: “Reaction of Crystalline Fluoro Olefins with Bromine Vapour.” Journal of Organic Chemistry, vol. 42, No. 10, 1977, pp. 1780-1783, p. 1781, compound 4.
M.W. Renoll: “Vinyl Aromatic Compounds III, Fluorinated Derivatives.” Journal of the Americal Chemical Society, vol. 68, 1946, pp. 1159-1161, p. 1159, compound 2.
H. Cousse et al.: “Synthese, structure et activite hypocholereroleminante d'une serie d'acides gamma-aryl, gamma-oxo butyriques substitutes et derives.” European Journal of Medicinal Chemistry, vol. 22, 1987, pp. 45-57, tables, VI, VII.
D.C. Naae et al: “The solid-gas chlorinateion and bromination of a fluorinated olefin.” Tetrahedron Letters, vol. 32, 1976, pp. 2761-2764, XP001181810, p. 2762, table.
J.L Chanal et al.: “Comparison of the Metabolism and Pharmacokinetics of Metbufen and Itanoxone and their Analogues in Rats.” Arzneimittel Forschung, vol. 38, No. 10, 1988, pp. 1454-1460, XP002230049, p. 1781, compound 4.
D.G. Naae: “Reaction of Crystalline Fluoro Olefins with Bromine Vapour.” Journal of Organic Chemistry, vol. 42, No. 10, 1977, pp. 1780-1783, XP002230049, p. 1781, compound 4.
M.W. Renoll: “Vinyl Aromatic Compounds III. Fluorinated Derivatives.”, Journal of the American Chemical Society, vol. 68, 1946, pp. 1159-1161, XP001181808, p. 1159, compound 2.
H. Cousse et al: “Synthese, structure et activite hypocholereroleminate d'une serie d'acides gamma-aryl, gamma-oxo butyriques substitutes et derives,” European Journal of Medicinal Chemistry, vol. 22, 1987, pp. 45-57, XP001181809, Tables VI, VII.
Ehrenfreund Josef
Lamberth Clemens
Tobler Hans
Walter Harald
Gegick Rebecca
Kosack Joseph R.
Saeed Kamal A.
Syngenta Crop Protection Inc.
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