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    Substituted 5-phenyl pyrimidines I in therapy
    2.
    发明专利
    Substituted 5-phenyl pyrimidines I in therapy 未知

    公开(公告)号：ZA200707315B

    公开(公告)日：2008-11-26

    申请号：ZA200707315

    申请日：2007-08-29

    Applicant: BASF AG

    Inventor： JOACHIM RHEINHEIMER ,  THOMAS GROTE ,  BERND MUELLER ,  FRANK SCHIEWECK ,  ANJA SCHWOEGLER ,  THORSTEN JABS ,  CARSTEN BLETTNER ,  BARBARA NAVE

    IPC: A61K20090101 ,  C07D20090101

    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.

    TRIAZOLOPIRIMIDINAS FUNGICIDAS, PROCEDIMIENTOS PARA SU OBTENCION Y EL USO DE LAS MISMAS PARA COMBATIR HONGOS NOCIVOS, ASI COMO PRODUCTOS QUE LAS CONTIENEN
    8.
    发明专利
    TRIAZOLOPIRIMIDINAS FUNGICIDAS, PROCEDIMIENTOS PARA SU OBTENCION Y EL USO DE LAS MISMAS PARA COMBATIR HONGOS NOCIVOS, ASI COMO PRODUCTOS QUE LAS CONTIENEN 未知

    公开(公告)号：CO5611066A2

    公开(公告)日：2006-02-28

    申请号：CO04105369

    申请日：2004-10-20

    Applicant: BASF AG

    Inventor： TORMO BLASCO JORDI ,  CARSTEN BLETTNER ,  MULLER BERND ,  GEWEHR MARKUS ,  WASSILIOS GRAMMENOS ,  GROTE THOMAS ,  GYPSER ANDREAS ,  RHEINHEIMER JOACHIM ,  SCHAFER PETER ,  SCHIEWECK FRANK ,  ANJA SCHWOGLER ,  AMMERMANN EBERHARD ,  STRATHMANN SIGFRIED ,  LORENZ GISELA ,  STIERL REINHARD ,  SCHOFL ULRICH

    IPC: A01N43/90 ,  C07C255/57 ,  C07D487/04

    Abstract: 1.- Triazolopirimidinas de la fórmula Ien la que los sustituyentes tienen los significados siguientes:L1 significa ciano, S(=O)nA1 o C(=O)A2, dondeA1 es hidrógeno, hidroxi, alquilo-C1-C8, alquilamino-C1-C8 o di-(alquilC1-C8)amino;A2 es alcoxi-C1-C8, halógenoalcoxi-C1-C6 o uno de los grupos mencionados en A1;n es 0, 1 ó 2; L2,L3 significan hidrógeno o halógeno;L4,L5 significan hidrógeno, halógeno o alquilo-C1-C4;X es halógeno, ciano, alquilo-C1-C4, halógenoalquilo-C1-C4, alcoxi-C1-C4 o halógenoalcoxi-C1-C2;R1 es alquilo-C1-C8, halógenoalquilo-C1-C8, cicloalquilo-C3-C6, halógenocicloalquilo-C3-C6, alquenilo-C2-C8, alcadienilo-C4-C10, halógenoalquenilo-C2-C8, cicloalquenilo-C3-C6, alquinilo-C2-C8, halógenoalquinilo-C2-C8 o cicloalquinilo-C3-C6, fenilo, naftilo, o un heterociclo saturado, parcialmente insaturado o aromático de cinco a diez miembros, que contiene uno a cuatro heteroátomos del grupo O, N o S;R2 es hidrógeno o uno de los grupos mencionados para R1,R1 y R2 también pueden formar junto con el átomo de nitrógeno, con el que están ligados, un anillo de cinco o seis miembros, que puede estar interrumpido por un átomo del grupo O, N y S y/o llevar uno o varios sustituyentes del grupo halógeno, alquilo-C1-C6, halógenoalquilo-C1-C6 y oxi-alquilenoxi-C1-C3 o en el que un átomo de N y un átomo de C vecino pueden estar ligados mediante una cadena de alquileno-C1-C4;pudiendo R1 y/o R2 estar sustituidos por uno a cuatro grupos Ra iguales o diferentes:Ra es halógeno, ciano, nitro, hidroxi, C1-C6-alquilo-, halógenoalquiloC1-C6-, alquilcarbonilo-C1-C6, cicloalquilo-C3-C6-, alcoxi-C1-C6-, halógenoalcoxi-C1-C6-, alcoxicarbonilo-C1-C6-, alquiltio-C1-C6-, alquilamino-C1-C6-, di-alquilamino-C1-C6, alquenilo-C2-C6-, alqueniloxi-C2-C6, ...

    2-(pyridin-2-yl)-pyrimidines and their use for controlling pathogenic fungi
    9.
    发明专利
    2-(pyridin-2-yl)-pyrimidines and their use for controlling pathogenic fungi 未知

    公开(公告)号：ZA200701518B

    公开(公告)日：2008-12-31

    申请号：ZA200701518

    申请日：2007-02-21

    Applicant: BASF AG

    Inventor： WASSILIOS GRAMMENOS ,  THOMAS GROTE ,  CARSTEN BLETTNER ,  MARKUS GEWEHR ,  UDO HUENGER ,  BERND MUELLER ,  JOACHIM RHEINHEIMER ,  PETER SCHAEFER ,  FRANK SCHIEWECK ,  ANJA SCHWOEGLER ,  ULRICH SCHOEFL ,  HARALD KOEHLE ,  SIEGFRIED STRATHMANN ,  MARIA SCHRERER ,  REINHARD STIERL ,  JAN RETHER

    IPC: A01N20090101 ,  A01N43/54 ,  C07D20090101 ,  C07D401/04

    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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