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Pyridyloxyalkanoic Acid Amide Derivatives Useful As Fungicides

Abstract: Fungicidal compounds of the general formula (I): wherein X and Y are independently H, halo, C¿1-8? alkyl, C¿3-6? cycloalkyl, C¿2-8? alkenyl, C¿2-8? alkynyl, C¿1-8? alkoxy, C¿1-8? alkylthio, nitro, amino, mono- or di-(C¿1-6?)alkylamino, mono- or di-(C¿2-6?)alkenylamino, mono- or di-(C¿2-6?)alkynylamino, formylamino, C¿1-4? alkyl(formyl)amino, C¿1-4? alkylcarbonylamino, C¿1-4? alkyl(C¿1-4? alkylcarbonyl)amino, cyano, formyl, C¿1-4? alkylcarbonyl, C¿1-4? alkoxycarbonyl, aminocarbonyl, mono- or di-(C¿1-4?)alkylaminocarbonyl, carboxy, C¿1-4? alkylcarbonyloxy, aryl(C¿1-4?)alkylcarbonyloxy, C¿1-4? alkylsulphinyl, C¿1-4? alkylsulphonyl, C¿1-4? alkylsulphonyloxy, aryl, heteroaryl, aryloxy, arylthio, heteroaryloxy or heteroarylthio wherein any of the foregoing alkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, groups or moieties are optionally substituted; R?1¿ is phenyl, cyano, C¿1-4? alkyl, C¿2-4? alkenyl or C¿2-4? alkynyl in which the alkyl, alkenyl and alkynyl groups are optionally substituted on their terminal carbon atom with one, two or three halogen atoms, with a cyano group, with a C¿1-4? alkylcarbonyl group, with a C¿1-4? alkoxycarbonyl group or with a hydroxy group, or R?1¿ is alkoxyalkyl, alkylthioalkyl, alkylsulphinylalkyl or alkylsulphonylalkyl in which the total number of carbon atoms is 2 or 3; R?2¿ is H, C¿1-4? alkyl, C¿1-4? alkoxymethyl or benzyloxymethyl in which the phenyl ring of the benzyl moiety is optionally substituted with C¿1-4? alkoxy; R?3¿ and R?4¿ are independently H, C¿1-3? alkyl, C¿2-3? alkenyl or C¿2-3? alkynyl provided that both are not H and that when both are other than H their combined total of carbon atoms does not exceed 4, or R?3¿ and R?4¿ join with the carbon atom to which they are attached to form a 3 or 4 membered carbocyclic ring optionally containing one O, S or N atom and optionally substituted with halo or C¿1-4? alkyl; and R?5¿ is halo, C¿1-4? alkyl or C¿3-4? cycloalkyl in which the alkyl or cycloalkyl group is optionally substituted with halo, hydroxy, C¿1-6? alkoxy, C¿1-6? alkylthio, cyano, C¿1-4? alkylcarbonyloxy, aminocarbonyloxy, mono- or di(C¿1-4?)alkylaminocarbonyloxy, or tri(C¿1-4?)alkylsilyloxy. The compounds and compositions containing them are especially useful for combating fungal infections of plants.

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Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
18 May 2004
Publication Number
06/2007
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
Parent Application

Applicants

SYNGENTA LIMITED
EUROPEAN REGIONAL CENTRE, PRIESTLEY ROAD, SURREY RESEARCH PARK, GUILDFORD, SURREY GU2 7YH UNITED KINGDOM.
SYNGENTA PARTICIPATIONS AG
SCHWARZWALDALLEE 215, CH-4058 BASEL SWITZERLAND.

Inventors

1. WILLIAM GUY WHITTINGHAM
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
2. KEVIN ROBERT LAWSON
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
3. PAUL ANTHONY WORTHINGTON
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
4. CHARLES ADAM RUSSELL
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
5. ROGER SALMON
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
6. LESLIE FRANCIS MAY
SYNGENTA LIMITED, JEALOTT'S HILL INTERNATIONAL RESEARCH CENTRE, BRACKNELL, BERKSHIRE RG42 6EY UNITED KINGDOM.
7. MARIO JORG
SCHWARZWALDALLEE 215, CH-4058 BASEL SWITZERLAND.
8. PACHLATKO, JOHANNES, PAUL
SCHWARZWALDALLEE 215, CH-4058 BASEL SWITZERLAND.

Specification

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