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公开(公告)号:EA014098B1
公开(公告)日:2010-08-30
申请号:EA200701582
申请日:2006-01-30
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , GROTE THOMAS , MULLER BERND , NAVE BARBARA , SCHIEWECK FRANK , SCHWOGLER ANJA , JABS THORSTEN , BLETTNER CARSTEN
IPC: A61K31/506 , A61K31/505 , C07D239/42 , C07D239/48 , C07D401/04 , C07D403/04 , C07D417/04
Abstract: Настоящееизобретениеотноситсяк замещенным 5-фенилпиримидинамформулы I, которыенесутрадикал X в 4-ойпозициипиримидиновогокольца, радикал Y в 6-ойпозициипиримидиновогокольца, где X означаетгруппуформулы NRR, вкоторой Rозначает C-C-алкил, C-C-алкенил, C-C-галоалкил, C-C-циклоалкил, которыемогутбытьзамещены C-C-алкилом, Rозначаетводород, C-C-алкилили C-C-алкенил, радикал Y выбираетсяизгруппы, состоящейизгалогенаи С-С-алкилаи фармацевтическиприемлемымсолямзамещенного 5-фенилпиримидина I дляпримененияв терапииилилечениираковыхзаболеваний.
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公开(公告)号:MA28878B1
公开(公告)日:2007-09-03
申请号:MA29781
申请日:2007-03-28
Applicant: BASF AG
Inventor: BLETTNER CARSTEN , TORMO I BLASCO JORDI , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , DIETZ JOCHEN , SPEAKMAN JOHN-BRYAN , JABS THORSTEN , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , SCHERER MARIA , STIERL REINHARD
IPC: A01N43/90 , C07D239/00 , C07D249/00 , C07D487/04
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公开(公告)号:MA28672B1
公开(公告)日:2007-06-01
申请号:MA29544
申请日:2006-12-20
Applicant: BASF AG
Inventor: BLETTNER CARSTEN , SCHIEWECK FRANK , TORMO I BLASCO JORDI , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHWOEGLER ANJA , WAGNER OLIVER , SPEAKMAN JOHN-BRYAN , JABS THORSTEN , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , SCHERER MARIA , STIERL REINHARD
IPC: A01N43/90 , C07D487/04
Abstract: La présente invention se rapporte à de nouveaux composés triazolopyrimidine de la formule I dans laquelle: X est halogène, cyano, alkyle C1-C4, haloalkyle C1-C4, alkoxy C1-C4 ou haloalcoxy C1-C2 ; W est oxygène ou soufre; Y est O-R4 ou un groupe NR5R6; A est une liaison chimique ou un groupe CR7R8; et les variables L, R1 à R7 sont telles que définies dans la revendication 1. La présente inventron assure en outre l'utilisation des composés triazolopyrimidine de la formule I, leurs tautomères et leurs sels acceptables en agriculture pour lutter contre les champignons phytopathogéniques (= champignons nuisibles), et un procédé pour lutter contre les champignons phytopathogéniques, lequel procédé comprend le traitement des champignons ou des matériels, des plantes, du sol ou de la semence à protéger contre l'attaque des champignons avec une quantité efficace d'un composé de la formule I, un tautomère de I et/ou avec un sel acceptable en agriculture de I ou un de ses tautomères.
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公开(公告)号:MXPA06013943A
公开(公告)日:2007-03-15
申请号:MXPA06013943
申请日:2005-06-24
Applicant: BASF AG
Inventor: WAGNER OLIVER , MULLER BERND , GRAMMENOS WASSILIOS , GROTE THOMAS , GEWEHR MARKUS , JABS THORSTEN , STRATHMANN SIEGFRIED , SCHERER MARIA , RHEINHEIMER JOACHIM , SCHAFER PETER , STIERL REINHARD , SCHIEWECK FRANK , BLASCO JORDI TORMO I , SCHOFL ULRICH , BLETTNER CARSTEN , SCHWOGLER ANJA , SPEAKMAN JOHN-BRYAN
IPC: C07D487/04
Abstract: Nuevos compuestos de triazolopirimidina de la formula I (ver formula (I)) en donde: X es halogeno, ciano, alquilo C1-C4, haloalquilo C1-C4, alcoxi C1-C4 o haloalcoxi C1-C2 W es oxigeno o azufre; Y es O-R4 o un grupo NR5R6 A es un enlace quimico o un grupo CR7R8 y las variables L, R1 a R7 son como se define en la reivindicacion 1 El uso de los compuestos de triazolopirimidina de la formula 1, sus tautomeros y sus sales aceptables en agricultura para el control de hongos fitopatogenos (= hongos daninos) y un metodo para controlar hongos daninos fitopatogenos, en donde el metodo comprende tratar el hongo o los materiales, plantas, el suelo o las semillas que se protegen contra el ataque de hongos con una cantidad efectiva de un compuesto de la formula I, un tautomero de I y/o una sal de I de aceptacion en agricultura aceptable o su tautomero.
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公开(公告)号:PE04452006A1
公开(公告)日:2006-06-20
申请号:PE0010272005
申请日:2005-09-06
Applicant: BASF AG
Inventor: MULLER BERND , TORMO I BLASCO JORDI , GROTE THOMAS , SCHERER MARIA , STIERL REINHARD , STRATHMANN SIEGFRIED , SCHOFL ULRICH , SCHIEWECK FRANK , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , SCHAFER PETER , SCHWOGLER ANJA , SPEAKMAN JOHN-BRYAN , HUNGER UDO , DIETZ JOCHEN , JABS THORSTEN
IPC: A01N43/90 , C07D239/00 , C07D249/00 , C07D487/04
CPC classification number: A01N43/90 , A01N47/06 , A01N47/12 , A01N47/16 , C07D487/04
Abstract: SE REFIERE TRIAZOLOPIRIMIDINAS DE FORMULA (I), EN DONDE R1 ES H, ALQUILO(C1-C12), HALOGENOALQUILO(C1-C12), ENTRE OTROS; R2 ES ALQUILO(C1-C8), HALOGENOALQUILO(C1-C6), ALQUENILO(C2-C8), ENTRE OTROS; R3, R4, R5, R6, R7 SON INDEPENDIENTES Y SIGNIFICAN H, ALQUILO(C1-C8), HALOGENOALQUILO(C1-C6), ENTRE OTROS; P ES 0 Y 1; L ES HALOGENO, ALQUILO(C1-C4), HALOGENOALQUILO(C1-C2), ENTRE OTROS; M ES 1 A 5; X ES HALOGENO, CIANO, ALQUILO(C1-C4), ENTRE OTROS; Y ES O O S; Z ES H, ALQUILO(C1-C8), HALOGENOALQUILO(C1-C6), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-[5-CLORO-6-(2,4,6-TRIFLUORO-FENIL)-[1,2,4]TRIAZOLO[1,5-A]PIRIMIDIN-7-ILAMINO]BUTAN-1-OL, 2-[5-CLORO-6-(2,4,6-TRIFLUORO-FENIL)-[1,2,4]TRIAZOLO[1,5-A]PIRIMIDIN-7-ILAMINO]BUTILO, [5-CLORO-6-(2,4,6-TRIFLUORO-FENIL)-[1,2,4]TRIAZOLO[1,5-A]PIRIMIDIN-7-IL]-(1-ETOXIMETIL-PROPIL)-AMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION. ESTOS COMPUESTOS SE UTILIZAN CONTRA HONGOS FITOPATOGENOS
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公开(公告)号:AU5970500A
公开(公告)日:2001-01-09
申请号:AU5970500
申请日:2000-06-07
Applicant: BASF AG
Inventor: RADEMACHER WILHELM , SPEAKMAN JOHN-BRYAN , AMMERMANN EBERHARD , JABS THORSTEN , HERBERS KARIN
IPC: A01H1/00 , A01H5/00 , C12N5/10 , C12N9/02 , C12N15/09 , C12N15/29 , C12N15/53 , C12N15/82 , C12N15/11 , A01N65/00
Abstract: The invention relates to a method of increasing the resistance of cultivated plants to bacterial and fungal pathogens by producing a plant by means of molecular genetics in which the activity of the enzyme flavonone-3-hydroxylase is reduced.
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公开(公告)号:BRPI0607108A2
公开(公告)日:2010-03-09
申请号:BRPI0607108
申请日:2006-01-30
Applicant: BASF AG
Inventor: SCHIEWECK FRANK , GROTE THOMAS , NAVE BARBARA , SCHWIGLER ANJA , JABS THORSTEN , BLETTNER CARSTEN , RHEINHEIMER JOACHIM , MUELLER BERND
IPC: A61K31/506 , A61K31/505 , C07D239/42 , C07D239/48 , C07D401/04 , C07D403/04 , C07D417/04
Abstract: The present invention relates to substituted 5-phenyl pyrimidines I, which carry a radical X in the 4-position of the pyrimidine ring, a radical Y in the 6-position of the pyrimidine ring, the radical X denoting a group of the formula NR 1 R 2 , OR 1a or SR 1a , in which R 1 , R 2 , independently of each other, denote hydrogen, C 1 -C 10 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 10 -haloalkyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, phenyl, or 5- or 6-membered heteroaryl or 5- or 6-membered heterocyclyl, containing 1, 2, 3 or 4 nitrogen atoms or 1, 2 or 3 nitrogen atoms and one sulfur or oxygen atom as ring members, which radicals may be unsubstituted or may carry 1, 2, 3 or 4 radicals R a1 ; or the radical NR 1 R 2 may also form a 5- or 6-membered optionally substituted heterocyclic ring, containing 1, 2, 3 or 4 nitrogen atoms or 1, 2 or 3 nitrogen atoms and one sulfur or oxygen atom as ring members, which are non-adjacent to the nitrogen of NR 1 R 2 , in which two adjacent C atoms or one N atom and one adjacent C atom can be linked by a C 1 -C 4 -alkylene chain and wherein the heterocyclic ring may be unsubstituted or may carry 1, 2, 3 or 4 radicals R a1 as defined in claim 1 , R 1a has one of the meanings given for R 1 except for hydrogen; the radical Y being selected from the group consisting of halogen, cyano, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -alkoxy, C 3 -C 4 -alkenyloxy, C 3 -C 4 -alkynyloxy, C 1 -C 6 -alkylthio, di-(C 1 -C 6 -alkyl)amino or C 1 -C 6 -alkylamino, where the alkyl, alkenyl and alkynyl radicals of Y may be substituted by halogen, cyano, nitro, C 1 -C 2 -alkoxy or C 1 -C 4 -alkoxycarbonyl; and wherein the pyrimidine radical may also carry a radical different from hydrogen in the 2-position and wherein the phenyl ring in the 5-position of the pyrimidine ring may be unsubstituted or carry 1, 2, 3, 4 or 5 radicals L which are different from hydrogen, and the pharmaceutically acceptable salts substituted 5-phenyl pyrimidines for use in therapy, in particular in therapy or treatment of cancerous diseases.
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公开(公告)号:BRPI0512557A
公开(公告)日:2008-03-25
申请号:BRPI0512557
申请日:2005-06-24
Applicant: BASF AG
Inventor: BLETTNER CARSTEN , SCHIEWECK FRANK , BLASCO JORDI TORMO I , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , RHEINHEIMER JOACHIM , SCHOFER PETER , SCHWOEGLER ANJA , WAGNER OLIVER , SPEAKMAN JOHN-BRYAN , JABS THORSTEN , STRATHMANN SIEGFRIED , FL ULRICH SCH , SCHERER MARIA , STIERL REINHARD
IPC: C07D487/04 , A01N43/90
Abstract: The present invention relates to novel triazolopyrimidine compounds of the formula I in which: X is halogen, cyano, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy or C 1 -C 2 -haloalkoxy; W is oxygen or sulfur; Y is O-R 4 or a group NR 5 R 6 ; A is a chemical bond or a group CR 7 R 8 ; and the variables L, R 1 to R 7 are as defined in claim 1. The present invention furthermore provides the use of the triazolopyrimidine compounds of the formula I, their tautomers and their agriculturally acceptable salts for controlling phytopathogenic fungi (=harmful fungi) and a method for controlling phytopathogenic harmful fungi, which method comprises treating the fungi or the materials, plants, the soil or seed to be protected against fungal attack with an effective amount of a compound of the formula I, a tautomer of I and/or an agriculturally acceptable salt of I or a tautomer thereof.
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公开(公告)号:PE01122006A1
公开(公告)日:2006-03-24
申请号:PE0007352005
申请日:2005-06-24
Applicant: BASF AG
Inventor: MULLER BERND , TORMO I BLASCO JORDI , GROTE THOMAS , SCHIEWECK FRANK , GEWEHR MARKUS , GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , STRATHAMANN SIEGFRIED , STIERL REINHARD , SCHERER MARIA , SCHOFL ULRICH , JABS THORSTEN , SCHAFER PETER , WAGNER OLIVER , BLETTNER CARSTEN , SPEAKMAN JOHN-BRYAN , SCHWOGLER ANJA
IPC: A01N43/90 , A01N53/12 , C07D487/04
CPC classification number: A01N43/90 , C07D487/04
Abstract: SE REFIERE A UNA TRIAZOLOPIRIMIDINA DE FORMULA (I) , DONDE X ES HALOGENO, CIANO, ALQUILO C1-4, ENTRE OTROS; W ES -O-,-S-; Y ES O-R4 O UN GRUPO NR5R6, DONDE R4 ES H, ALQUILO C1-8, HIDROXIALQUILO C1-4, ENTRE OTROS; R5 Y R6 SON H, ALQUILO C1-8, CICLOALQUILO C3-6, ENTRE OTROS; A ES UN ENLACE QUIMICO O UN GRUPO CR7R8, DONDE R7 Y R8 SON H, ALQUILO C1-4, ALCOXI C1-4, ENTRE OTROS; L ES HALOGENO, ALQUILO C1-6, ALQUELINO C2-6, ENTRE OTROS; M ES 0 A 5 ; R3 ES H, ALQUILO C1-4, ALCOXI C1-4, ENTRE OTROS, R2 ES H, ALCOXI C1-4, HALOALQUILO C1-4, ENTRE OTROS; R1 ES H, ALQUILO C1-4, FORMILO, ENTRE OTROS. UN COMPUESTO PREFERIDO ES LA FORMULA (II). SE REFIERE A COMPUESTOS DE TRIAZOLOPIRIMIDINAS UTIL EN EL CONTROL DE HONGOS DANINOS FITOPATOGENOS
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公开(公告)号:CA2577041A1
公开(公告)日:2006-03-16
申请号:CA2577041
申请日:2005-09-02
Applicant: BASF AG
Inventor: STRATHMANN SIEGFRIED , BLETTNER CARSTEN , SCHOEFL ULRICH , GEWEHR MARKUS , TORMO I BLASCO JORDI , SCHERER MARIA , STIERL REINHARD , MUELLER BERND , SCHIEWECK FRANK , GRAMMENOS WASSILIOS , JABS THORSTEN , SPEAKMAN JOHN-BRYAN , GROTE THOMAS , HUENGER UDO , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHWOEGLER ANJA , DIETZ JOCHEN
IPC: C07D487/04 , A01N43/90 , C07D239/00 , C07D249/00
Abstract: 6-Phenyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below: R 1 is 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 comprises one to four heteroatoms from the group consisting of O, N and S, R 2 is 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 comprises one to four heteroatoms from the group consisting of O, N and S, R 3 ,R 4 ,R 5 ,R 6 ,R 7 are hydrogen or one of the groups mentioned under R 2 , R 4 , together with R 3 or R 6 , may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms, may comprise one to three further heteroatoms from the group consisting of O, N and S as ring members; R 2 with R 3 , R 4 with R 5 , R 6 with R 7 may in each case together, with formation of spiro groups, also form a C 2 -C 5 -alkylene, or alkenylene or alkynylene chain which may be interrupted by one to three heteroatoms from the group consisting of O, N and S; p is zero or 1; L is halogen, alkyl, haloalkyl, alkoxy, cyano, nitro, amino, alkylamino, dialkylamino, alkylcarbonylamino, C(O)-R, S(O) n -R; where n is zero, 1 or 2; R is hydrogen, alkyl, haloalkyl, alkoxy, alkenyloxy, alkynyloxy, amino, alkylamino, dialkylamino; m is 1, 2, 3, 4 or 5; X is halogen, cyano, alkyl, alkoxy, alkenyloxy, alkynyloxy or haloalkoxy; Y is oxygen or sulfur; Z is hydrogen, alkyl, haloalkyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, alkenyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl, phenyl, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S; or Z together with R 4 or R 6 may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms and Y, may comprise one or two further heteroatoms from the group consisting of O, N and S as ring members the groups R 1 to R 7 , Z and R may be substituted according to the description; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
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