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公开(公告)号:AU2005266555A1
公开(公告)日:2006-02-02
申请号:AU2005266555
申请日:2005-07-22
Applicant: BASF AG
Inventor: GROTE THOMAS , MULLER BERND , STIERL REINHARD , RHEINHEIMER JOACHIM , SCHWOGLER ANJA , GRAMMENOS WASSILIOS , SCHERER MARIA , SCHOFL ULRICH , GEWEHR MARKUS , SCHAFER PETER , STRATHMANN SIEGFRIED , RETHER JAN , BLETTNER CARSTEN , HUNGER UDO , SCHIEWECK FRANK , KOHLE HARALD
IPC: C07D401/04 , A01N43/54
Abstract: 2-Pyridyl pyrimidine derivatives (I) are new. 2-Pyridyl pyrimidine derivatives of formula (I) and their salts are new. k : 0-3; m : 0-5; n : 1-5; R 1>halo, OH, CN, NO 2, 1-4C (halo)alkyl, 104C (halo)alkoxy, 2-4C alkenyl, 2-4C alkynyl, 3-8C cycloalkyl, (1-4C)alkoxy(1-4C)alkyl, NH 2, phenoxy (optionally substituted with halo or 1-4C alkyl), NHR, NRR, C(Ra)=NORb, SO pA 1> or COA 2>; or R 1>+R 1>1-4C (halo)alkylenedioxy; R : 1-4C alkyl or 1-4C alkylcarbonyl; Ra : H or 1-4C alkyl; Rb : 1-4C alkyl, 3-4C alkenyl or 3-4C alkynyl; p : 0-2; A 1>1-4C alkyl, or also NH 2, 1-4C alkylamino or di(1-4C alkyl)amino when p = 2; A 2>H, OH, 1-4C alkyl, 1-4C alkylamino, di(1-4C alkyl)amino, 2-4C alkenyl or 1-4C (halo)alkoxy; R 2>1-4C haloalkyl, 1-4C (halo)alkoxy, OH, halo, CN or NO 2, or R 2> can be H or 1-4C alkyl if n = 3-5 and/or k = 1-3 and/or at least one R 1> is other than halo, 1-4C (halo)alkyl and 1-4C alkoxy; and R 3>1-4C alkyl. An independent claim is also included for controlling phytopathogenic fungi by treating the fungi, or materials, plants, soil or seeds to be protected from fungal attack, with a compound (I). [Image] ACTIVITY : Plant antifungal. In a protective test against Alternaria solani on tomato plants, plants treated with 2-(5-methyl-6-phenyl-2-pyridyl)-4,5-pentamethylene-pyrimidine (250 ppm) suffered no attack, whereas 90% of untreated plants were attacked. MECHANISM OF ACTION : None given.
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公开(公告)号:PE20050882A1
公开(公告)日:2005-12-01
申请号:PE2004000707
申请日:2004-07-22
Applicant: BASF AG
Inventor: SCHWOGLER ANJA , GEWEHR MARKUS , MULLER BERND , GROTE THOMAS , GRAMMENOS WASSILIOS , TORMO I BLASCO JORDI , GYPSER ANDREAS , RHEINHEIMER JOACHIM , BLETTNER CARSTEN , SCHAFER PETER , SCHIEWECK FRANK , WAGNER OLIVER , STIERL REINHARD , SCHOFL ULRICH , STRATHMANN SIEGFRIED , SCHERER MARIA
IPC: C07D239/42
Abstract: DE FORMULA (I), DONDE: n ES UN NUMERO ENTERO DE 1 A 5; L ES HALOGENO, CIANO, CIANATO, ALQUILO C1-C8, ALQUENILO o ALQUINILO o ALQUENILOXI o ALQUINILOXI C2-C8, ALCOXI C1-C6, CICLOALQUILO o CICLOALQUILOXI C3-C6, CICLOALQUENILO C4-C6, NITRO, -C(=O)-A, -C(=O)-O-A, -C(=O)-N(A')A, C(A')(=N-OA), N(A')A, N(A')-C(=O)-A, N(A")-C(=O)-N(A')A, S(=O)m-A, S(=O)m-O-A o S(=O)m-N(A')A, PUDIENDO LOS GRUPOS ALIFATICOS DE L ESTAR PARCIAL O COMPLETAMENTE HALOGENADOS; m ES 0, 1 o 2; A, A', A'' SON H, ALQUILO C1-C6, ALQUENILO o ALQUINILO C2-C6, CICLOALQUILO o CICLOALQUENILO C3-C8, FENILO, CON RADICALES ORGANICOS PARCIAL O COMPLETAMENTE HALOGENADOS O SUSTITUIDOS POR NITRO, CIANATO, CIANO O ALCOXI C1-C4; R1, R2 SON ALQUILO C1-C6, ALQUENILO o ALQUINILO C2-C6, CICLOALQUILO o HALOGENOCICLOAQUILO C3-C6, ENTRE OTROS; R3 ES HALOGENO, CIANO, ALQUILO C1-C4, ALQUENILO o ALQUINILO C2-C4, CICLOALQUILO C3-C6, ALCOXI C1-C4, ALQUENILOXI o ALQUINILOXI C3-C4, ALQUILTIO C1-C6, ENTRE OTROS, PUDIENDO LOS GRUPOS ALIFATICOS DE R1 Y R2 ESTAR PARCIAL O COMPLETAMENTE HALOGENADOS; R4 CORRESPONDE A LAS FORMULAS (II) o (III) DONDE: X ES -(C=O), -(C=O)-NH, -(C=O)-O, -O, -NRc ENTRE OTROS; Ra ES H, ALQUILO C1-C6, ALQUENILO o ALQUINILO C2-C8, o BENCILO; Rb ES H, ALQUILO C1-C6, ALQUENILO o ALQUINILO C2-C6; Rc ES H, ALQUILO C1-C6, ALQUENILO O ALQUINILO C2-C6, BENCILO O ACILO C1-C6. ADEMAS SE REFIERE A UN PRODUCTO PESTICIDA QUE CONTIENE UN SOPORTE SOLIDO O LIQUIDO Y EL COMPUESTO DE FORMULA (I),PARA COMBATIR HONGOS NOCIVOS FITOPATOGENOS
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公开(公告)号:PE08122005A1
公开(公告)日:2005-11-03
申请号:PE0000082005
申请日:2005-01-03
Applicant: BASF AG
Inventor: TORMO I BLASCO JORDI , BLETTNER CARSTEN , MULLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , WAGNER OLIVIER , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOFL ULRICH , STIERL REINHARD
IPC: A01N43/653 , C07D487/04
CPC classification number: C07D487/04 , A01N43/90
Abstract: SE REFIERE A TRIAZOLOPIRIMIDINAS DE FORMULA (I), DONDE L ES H, CLORO O BROMO; R1 Y R2 SON INDEPENDIENTEMENTE ALQUILO C1-C8, HALOGENOALQUILO C1-C8. CICLOALQUILO C3-C8 o FENILO, NAFTILO o UN HETEROCICLO SATURADO, PARCIALMENTE INSATURADO O AROMATICO, CON 5 o 6 MIEMBROS, QUE CONTIENEN UNO A CUATRO HETEROATOMOS DEL GRUPO: O, N o S; R3 ES ALQUILO C1-C8, HALOGENOALQUILO C1-C8, ALQUENILO C3-C8, HALOGENOALQUILO C-C8, ALQUINILO C3-C8, ENTRE OTROS; DONDE R1 Y/O R2 PUEDEN LLEVAR 1 A 4 GRUPOS Ra, SIENDO Ra HALOGENO, CIANO, NITRO, HIDROXI, ALQUILO C1-C6, HALOGENOALQUILO, FENILO, NAFTILO, HETEROCICLO SATURADO, PARCIALMENTE INSATURADO O AROMATICO DE CINCO o DIEZ MIEMBROS, QUE CONTIENE UNO A CUATRO HETEROATOMOS DE: O, N o S, PUDIENDO ESTOS GRUPOS ALIFATICOS, ALICICLICOS o AROMATICOS POR SU PARTE ESTAR PARCIAL O COMPLETAMENTE HALOGENADOS O LLEVAR UNO A TRES GRUPOS Rb; DONDE Rb ES HALOGENO, CIANO, NITRO, MERCAPTO, AMINO, ALCOXI, FORMILO, ALQUILCARBONILO, ALQUILCARBONILOXI, DIALQUILAMINOTIOCARBONILO, ENTRE OTROS, CONTENIENDO LOS GRUPOS ALQUILO 1 A 6 ATOMOS DE CARBONO Y LOS GRUPOS ALQUENILO O ALQUINILO MENCIONADOS DE A 8 ATOMOS DE CARBONO; Y, UNO A TRES DE LOS RADICALES SIGUIENTES: CICLOALQUILO, CICLOALCOXI, DONDE, LOS SISTEMAS CICLICOS PUEDEN CONTENER 3 A 10 MIEMBROS ANULARES, ARILO, ARILOXI, ARILTIO, ARIL-ALCOXI C1-C6, HETARILOXI, ENTRE OTROS; Y, X ES HALOGENO, CIANO, ALQUILO C1-C4, HALOGENOALQUILO C1-C4, ALCOXI C1-C4, ENTRE OTROS. TIENE APLICACION PARA COMBATIR HONGOS NOCIVOS
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公开(公告)号:NZ531169A
公开(公告)日:2005-09-30
申请号:NZ53116902
申请日:2002-07-16
Applicant: BASF AG
Inventor: TORMO I BLASCO JORDI , SAUTER HUBERT , MULLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC: A01N43/90 , C07D487/04 , C07D249/00 , C07D239/00
Abstract: Disclosed are 7-aminotriazolopyrimidine compounds of formula I, wherein: R1 and R2 are independently H, alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, naphthyl, heterocyclyl, or heteroaryl, or R1 and R2 together may form a heterocyclic ring, R3 is alkyl, alkenyl, alkynyl, cycloalkyl, phenyl-alkyl, or haloalkyl, X is halo, cyano, alkoxy, haloalkyl, or phenyl. The compounds are used for preparing compositions suitable for controlling harmful fungi.
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公开(公告)号:CO5550500A2
公开(公告)日:2005-08-31
申请号:CO04002809
申请日:2004-01-16
Applicant: BASF AG
Inventor: TORMO BLASCO JORDI , HUBERT SAUTER , MULLER BERND , GEWEHR MARKUS , WASSILIOS GRAMMENOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , INGO ROSE , SCHAFER PETER , SCHIEWECK FRANK , RACK MICHAEL , MERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC: A01N43/90 , C07D487/04
Abstract: 1.- 6-(2-tolil)-triazolopirimidinas sustituidas de la fórmula IEn la cualR1 y R2 independientemente significan hidrogeno o alquiloC1-C10, alquenilo C2-C10, alquenilo C2-C10, o alcadienilo C4-C10, haloalquilo C2-C10, haloalquenilo C2-C10, o cicloalquilo C3-C10, fenilo, naftilo, oheterociclilo de 5 o 6 miembros, que contiene de 1 a 4 átomos de nitrógeno o 1 a 3 átomos de nitrógeno y un átomo de azufre u oxígeno, oheteroarilo 5 o 6 miembros que contiene 1 a 4 átomos de nitrógeno o 1 a 3 átomos de nitrógeno y un átomo de azufre u oxígeno, odonde los radicales R1 y R2 pueden ser no sustituidos o parcial o completamente halogenados o pueden llevar 1 a 3 grupos Ra,Ra es ciano, nitro, hidroxilo, alquilo C1-C6, cicloalquilo C3-C6, alcoxi C1-C6, alquiltio C1-C6, alquilamino C1-C6, di-C1-C6 alquilamino, alquenilo C2-C6, alqueniloxi C2-C6, alquinilo C2-C6, alquiniloxi C3-C6 y alquilenedioxi C1-C4;oR1 y R2 juntos con el átomo de nitrógeno interyacente representan un anillo heterocíclico de 5 o 6 miembros, que contiene 1 a 4 átomos de nitrógeno o 1 a 3 átomos de nitrógeno y un átomo de azufre u oxígeno, que puede ser sustituido por 1 a 3 radicales Ra; R3 es halógeno, ciano, alquilo C1-C10, alcoxi C1-C10, haloalquilo C1-C10, o C(=O)A, en dondeA es halógeno, hidroxi, alquilo C1-C8, alcoxi C1-C8, amino, alquilamino C1-C8, o di- (alquil C1-C8)-amino;N es un entero de 1 a 4; yX es halógeno, ciano, alquilo C1-C6, alcoxi C1-C6, haloalcoxi C1-C6 o alqueniloxi C3-C8.
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公开(公告)号:AU2004299255A1
公开(公告)日:2005-06-30
申请号:AU2004299255
申请日:2004-12-15
Applicant: BASF AG
Inventor: SCHOFL ULRICH , SCHIEWECK FRANK , MULLER BERND , SCHWOGLER ANJA , STIERL REINHARD , SCHAFER PETER , BLETTNER CARSTEN , RHEINHEIMER JOACHIM , WAGNER OLIVER , GROTE THOMAS , SCHERER MARIA , STRATHMANN SIEGFRIED , GRAMMENOS WASSILIOS , GEWEHR MARKUS , BLASCO JORDI TORMO I
IPC: C07D487/04
Abstract: Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: L is hydrogen, chlorine or bromine; R 1 , R 2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R 1 and R 2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain a further heteroatom from the group consisting of O, N and S as ring member and/or may be substituted as defined in the description; R 3 is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkyl, halocycloalkyl or phenylalkyl; R 1 , R 2 and/or R 3 may be substituted as defined in the description; X is halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
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公开(公告)号:AU2004242850A1
公开(公告)日:2004-12-09
申请号:AU2004242850
申请日:2004-05-27
Applicant: BASF AG
Inventor: SCHWOGLER ANJA , STRATHMANN SIEGFRIED , SPEAKMAN JOHN-BRYAN , GROTE THOMAS , GYPSER ANDREAS , SCHIEWECK FRANK , STIERL REINHARD , BLETTNER CARSTEN , AKERS ALAN , MULLER BERND , SCHERER MARIA , GEWEHR MARKUS , SCHAFER PETER , RHEINHEIMER JOACHIM , SCHOFL ULRICH , RACK MICHAEL , WAGNER OLIVER , BLASCO JORDI TORMO I , GRAMMENOS WASSILIOS
IPC: C07D487/04 , A01N43/90
Abstract: The invention relates to substituted pyrazolopyrimidines of formula (I) wherein the substituents have the following designations: L represents halogen, alkyl, halogenalkyl, alkenyl, alkoxy, amino, NHR, NR 2 , cyano, S(-O) n A 1 or C(-O)A 2 , R representing alkyl or alkylcarbonyl, A 1 representing hydrogen, hydroxy, alkyl, alkylamino or dialkylamino, n representing 0, 1 or 2, and A 2 representing alkenyl, alkoxy, halogenalkoxy or one of the groups cited for A 1 ; m represents 0 or 1 to 5; R 1 represents alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, alkadienyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl, phenyl, naphthyl, or a five-membered to ten-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group O, N or S; and R 2 represents hydrogen or one of the groups cited for R 1 . Together with the nitrogen atom to which they are bonded, R 1 and R 2 can form a five-membered to six-membered ring that can be interrupted by an atom from the groups O, N and S, and R 1 and/or R 2 can also be substituted according to the description. Furthermore, in formula (I): X represents halogen, cyano, OH, alkyl, alkoxy or halogenalkoxy; Y represents a five-membered to ten-membered saturated, partially unsaturated or aromatic heterocycle according to the description, or a group X or another group according to the description; p represents 1 or 2, the groups Y being potentially different when p=2; and p represents 0, when X is according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing the same, and the use thereof for controlling phytopathogenic fungi.
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公开(公告)号:AU2003296662A1
公开(公告)日:2004-07-22
申请号:AU2003296662
申请日:2003-12-17
Applicant: BASF AG
Inventor: MULLER BERND , BLASCO JORDI TORMO I , GROTE THOMAS , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , SCHOFL ULRICH , STIERL REINHARD
IPC: A01N43/90 , C07D487/04
Abstract: Triazolopyrimidines of the formula I in which the index n and the substituents R 1 , R 2 and R 3 are as defined in the description, and processes for preparing these compounds, compositions comprising them and their use for controlling harmful fungi are described.
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公开(公告)号:SK14002003A3
公开(公告)日:2004-06-08
申请号:SK14002003
申请日:2002-05-17
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , GYPSER ANDREAS , ROSE INGO , GROTE THOMAS , SCHAFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , SPEAKMAN JOHN-BRYAN , STRATHMANN SIEGFRIED , LORENZ GISELA
IPC: A01N43/86 , A01N43/90 , C07D265/24 , C07D498/04 , C07D513/04
Abstract: Oxazin(ethi)one compounds of the formula I: in which the variables Z, R 1 , R 2 , R 3 and n are as defined in claim 1 and A is a 5- or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1, 2 or 3 heteroatoms selected from the group consisting of N, O and S, each of which cycles is attached via two carbon atoms to the oxazin(ethi)one ring, and the agriculturally useful salts of the oxazin(ethi)one compounds I are described. Moreover, the invention describes the use of compounds I and their salts for controlling phytopathogenic fungi, compositions which comprise the compounds I and/or their salts in a fungicidally effective amount and a method for controlling phytopathogenic fungi which comprises treating the fungi or the materials, plants, seeds or the soil threatened by fungal attack with a fungicidally effective amount of at least one compound of the formula I as claimed in claim 1 and/or a salt of I.
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公开(公告)号:AU2003232227A1
公开(公告)日:2003-11-17
申请号:AU2003232227
申请日:2003-04-30
Applicant: BASF AG
Inventor: GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHIEWECK FRANK , SCHWOGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD , BLASCO JORDI TORMO I , BLETTNER CARSTEN , MULLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS
IPC: A01N43/90 , C07C69/65 , C07D487/04 , C07C69/612 , C07C69/738
Abstract: Disclosed are a method for producing fungicidal triazolopyrimidine compounds, agents containing said compounds, and the use thereof for controlling harmful fungi. Also disclosed are triazolopyrimidines of formula (1), in which the substituents have the following meaning: L 1 represents alkyl; L 2 represents halogen; L 3 represents hydrogen or halogen; X represents halogen, cyano, alkyl, alkoxy, or haloalkoxy; R 1 , R 2 represent hydrogen, alkyl, haloalkyl, cycloalkyl, alkenyl, alkadienyl, alkinyl, or cycloalkinyl, phenyl, naphthyl, or a five-unit to ten-unit saturated, partially unsaturated, or aromatic heterocycle containing one to four heteroatoms from the group O, N, or S. R 1 and R 2 can also form a five-unit or six-unit ring along with the nitrogen atom to which they are linked. Said ring can be interrupted and/or substituted by an atom from the group O, N, and S while R 1 and/or R 2 can be substituted according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing said compounds, and the use thereof for controlling harmful fungi.
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