2-(PIRIDIN-2-IL)-PIRIMIDINAS Y SU USO PARA COMBATIR HONGOS DANINOS.

    公开(公告)号:MX2007000620A

    公开(公告)日:2007-03-30

    申请号:MX2007000620

    申请日:2005-07-22

    Applicant: BASF AG

    Abstract: Compuestos de 2-(piridin--2-il)-pirimidinas de la formula general 1 y su uso para combatir hongos daninos, asi como los agentes fitosanitarios que contienen estos compuestos como componente activo. aqui, k esO, 1,2,63, mes 0, 1,2,3,4 o 5, n es 1,2,3,4,65; R1 es, de modo independiente entre si, halogeno, OH, CN, NO2, alquilo C-C4, halogenalquilo C1-C4, alcoxi C1-C4, halogenalcoxi C1-C4, alquenilo C2-C4, alquinilo C2-C4, cicloalquilo C3-C8, alcoxi C1-C4-alquilo C1-C4, amino, fenoxi, que eventualmente esta sustituido por halogeno o alquilo C1-C4, NHR, NR2, C(Ra)=N_ ORb, S(=O)A1 o C(=O)A2, o dos radicales R1 unidos a atomos de C adyacentes tambien pueden ser juntos un grupo -O-Alk-O-, en donde Alk es alquileno C-C4 lineal o ramificado, en donde 1, 2, 3 6 4 atomos de hidrogeno tambien pueden estar reemplazados por halogeno; R2 es halogenalquilo C1-C4, alcoxi C1-C4, halogenalcoxi C1-C4, hidroxi, halogeno, CN o NO2 en donde R2 tambien puede ser hidrogeno o alquilo C1-C4, cuando se cumple al menos una de las tres condiciones siguientes: - nes3,4o5, - kesl,263, - para m O, al menos uno de los radicales R1 es un radical distinto de halogeno, alquilo C1-C4, alcoxi C1-C4 y halogenalquilo C1-C4 yR3 es alquilo C1-C4.

    124.
    发明专利
    未知

    公开(公告)号:AT353901T

    公开(公告)日:2007-03-15

    申请号:AT02758297

    申请日:2002-07-03

    Applicant: BASF AG

    Abstract: 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines (I) are new. 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines of formula (I) are new. [Image] n : 0-5; R : halo, CN, OH or OCN, or alkyl, alkenyl, alkynyl, T', haloalkenyl, OT, alkenyloxy, alkynyloxy, OT', cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, CONH 2, mono- or dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkynyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, cycloalkylcarbonyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); T : 1-6C alkyl; T' : 1-6C haloalkyl; Het : 5-10 membered, saturated, partially unsaturated or aromatic heterocycle containing 1-4 of O, N and/or S heteroatoms; R 11-10C alkyl, alkenyl, alkynyl, 3-12C cycloalkyl, 3-10C cycloalkenyl, phenyl, naphthyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); R ahalo, CN, NO 2, OH, T, T', COT, cycloalkyl, OT, OT', COOT, NHT, NT 2, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C alkynyloxy, alkoximino, alkenyloximino, alkynyloximino, aralkoximino, alkynyl, alkynyloxycarbonyl, phenyl, naphthyl or Het (where all aliphatic, alicyclic or aromatic groups are optionally partially or completely halogenated and optionally substituted by 1-3 R aand/or 1-3 R c); R bhalo, CN, NO 2, OH, SH, NH 2, COOH, CONH 2, CSNH 2, T, T', 2-8C alkenyl, 2-8C alkenyloxy, 2-8C alkynyloxy, OT, OT', ST, NHT, NT 2, CHO, COT, SO 2T, SOT, COOT, OCOT, CONHT, CONT 2, CSNHT or CSNT 2; R ccycloalkyl, -O-cycloalkyl, heterocyclyl, -O-heterocyclyl, aryl, -O-aryl, -S-aryl, -O-T-aryl, -T-aryl, heteroaryl, -O-heteroaryl or -S-heteroaryl (where cycloalkyl or heterocyclyl rings are 3-10 membered, aryl rings are preferably 6-10 membered and heteroaryl rings are preferably 5-6 membered; and all rings are optionally partially or completely halogenated and optionally substituted by alkyl or haloalkyl); and R 21-4C alkyl, 2-4C alkynyl or 2-4C alkynyl (all optionally substituted by halo, CN, NO 2, OMe, OEt or 1-4C alkoxycarbonyl; Unless specified otherwise alkyl moieties have 1-8C, alkenyl or alkynyl moieties 2-10C and cycloalkyl or cycloalkenyl moieties 3-6C. Independent claims are also included for: (1) preparation of (I); and (2) dicarbonyl compound intermediates of formula (III), provided that n is not 0 and R 1and R 2are not both Me. [Image] ACTIVITY : Fungicide. 7-Cyclohexyl-5-methyl-6-(2-chloro-6-fluorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine (Ia) at a concentration of 63 ppm gave at least 90 % protection of tomato plants against Alternaria solani. MECHANISM OF ACTION : None given.

    ФУНГИЦИДНЫЕ СМЕСИ
    125.
    发明专利

    公开(公告)号:EA007925B1

    公开(公告)日:2007-02-27

    申请号:EA200500705

    申请日:2003-11-14

    Applicant: BASF AG

    Abstract: Фунгицидныесмеси, содержащиеА) производноетриазолопиримидинаформулы IиВ) карбаматыформулы IIвкоторой n равно 1 или 2, и X означаетгалоген, С-Салкили С-Сгалогеналкил, причемостатки X могутбытьразличными, если n равно 2, всинергическиэффективномколичестве, способборьбыс фитопатогеннымигрибамисмесямисоединений I и II, содержащееихсредствои применениесоединения I исоединения II дляполученияподобныхсмесей.

    ФУНГИЦИДНЫЕ СМЕСИ НА БАЗЕ ПРОИЗВОДНЫХ ИМИДАЗОЛА

    公开(公告)号:EA007899B1

    公开(公告)日:2007-02-27

    申请号:EA200500710

    申请日:2003-11-14

    Applicant: BASF AG

    Abstract: Фунгицидныесмеси, содержащие: А) триазолопиримидинформулы IиВ) производныеимидазолаформулы IIвкоторой Xи Xозначаютгалогени фенил, которыйможетбытьзамещенгалогеномилиалкилом, или Xи Xвместес соединяющеймостикомуглерод-углероднойдвойнойсвязьюобразуютдифторметилендиоксифенильнуюгруппу; Xозначаетцианоилигалогени Xозначаетдиалкилтиоилиизоксазол-4-ил, которыйможетиметьдваалкильныхостатка, всинергическиэффективномколичестве, способборьбыс фитопатогеннымигрибамисмесямисоединений I и II, содержащиеихсредстваи применениесоединений I и II дляполученияподобныхсмесей.

    MEZCLAS FUNGICIDAS
    130.
    发明专利

    公开(公告)号:ECSP066945A

    公开(公告)日:2007-01-26

    申请号:ECSP066945

    申请日:2006-10-23

    Applicant: BASF AG

    Abstract: Mezclas fungicidas, que contienen como componentes activos: 1) el derivado de tiazolopirimidina de la fórmula I, y2) pirifenox de la fórmula II, en una cantidad sinergética activa, procedimiento para combatir hongos nocivos fitopatógenos con mezclas del compuesto I con el compuesto II y el uso de los compuestos I y II para la preparación de tales mezclas, así como productos que contienen estas mezclas.

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