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    QUINOLINE DERIVATIVES AND THEIR USE AS PESTICIDES
    122.
    发明专利
    QUINOLINE DERIVATIVES AND THEIR USE AS PESTICIDES 未知

    公开(公告)号：CA2645069A1

    公开(公告)日：2007-09-20

    申请号：CA2645069

    申请日：2007-03-12

    Applicant: BASF SE

    Inventor： KUHN DAVID G ,  PUHL MICHAEL ,  GRAMMENOS WASSILIOS ,  VAN TUYL COTTER HENRY ,  RHEINHEIMER JOACHIM ,  LOHMANN JAN KLAAS ,  OLOUMI-SADEGHI HASSAN ,  LANGEWALD JUERGEN ,  KORADIN CHRISTOPHER ,  CULBERTSON DEBORAH L ,  RACK MICHAEL ,  ANSPAUGH DOUGLAS D ,  PARRA RAPADO LILIANA

    IPC: C07D215/12 ,  A01N43/42 ,  C07D215/60

    Abstract: This invention relates to quinoline derivatives of formula I wherein R1, R2, R3 are each independently halogen, hydroxy, cyano, amino, nitro, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, C1-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C1-C4-alkoxy-C1-C4-alkoxy, C3-C7-cycloalkyl-C1-C4-alkoxy, C(OH)(CF3)2, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, C(Ra)-O, C(Ra)-NORb, C(-O)ORx, or C(-O)NRxRy; Ra is hydrogen or C1-C4-alkyl; Rb is hydrogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, or C2-C4-haloalkenyl; Rx, Ry are each independently hydrogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-thioalkyl-C1-C4-alkyl, C1-C4-alkyl-S(-O)C1-C4-alkyl, C1-C4-alkyl-S(-O)2C1-C4-alkyl, C3-C6-cyloalkyl, C1-C4-alkyl-C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl; R4, R5, R6, R7 are each independently hydrogen, halogen, cyano, amino, nitro, hydroxy, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, or C(-O)ORc; Rc is hydrogen, C1-C6-alkyl, C2-C6-alkenyl, or C2-C6-alkinyl; m and n are each independently 1, 2, 3, 4, or 5; p is 0, 1, 2, 3, 4, or 5; and the N-oxides, enantiomers, diastereomers and salts thereof, processes and intermediates for the preparation of compounds I, use of compounds I for combating insects, acarids, or nematodes and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds I.

    METHOD FOR MANUFACTURING ARYL CARBOXAMIDES
    128.
    发明专利
    METHOD FOR MANUFACTURING ARYL CARBOXAMIDES 未知

    公开(公告)号：CA2721695C

    公开(公告)日：2016-04-12

    申请号：CA2721695

    申请日：2009-05-06

    Applicant: BASF SE

    Inventor： REICHERT WOLFGANG ,  KORADIN CHRISTOPHER ,  SMIDT SEBASTIAN PEER ,  MAYWALD VOLKER ,  WOLF BERND ,  RACK MICHAEL ,  ZIERKE THOMAS ,  KEIL MICHAEL

    IPC: C07D213/82 ,  C07C231/02 ,  C07C233/57 ,  C07C233/64 ,  C07D231/14 ,  C07D231/16

    Abstract: Method for manufacturing aryl carboxamides of the formula (I), with Ar = singly to triply substituted phenyl , pyridyl or pyrazolyl rings, wherein the substituents are selected from halogen, C1-C4 alkyl and C1-C4 halogen alkyl; M = thienyl or phenyl, which can contain a halogen substituent; Q = direct bond, cyclopropylene, annulated bicyclo [2.2.1]heptane or bicyclo[2.2.1]heptene ring; R1 = hydrogen, halogen, C1-C6 alkyl, C1-C4 alkoxy, C1-C4 halogen alkoxy, singly to triply substituted phenyl, wherein the substituents are selected from halogen and trifluoromethylthio, or cyclopropyl; through reaction of an acid chloride of the formula (II) with an aryl amine (III) in a suitable non-aqueous solvent, wherein in the absence of an auxiliary base a) the acid chloride (II) is added, b) a pressure of 0 to 700 mbar is established, c) the aryl amine (III) is added in approximately stoichiometric amounts and d) the valuable product is isolated.

    Method for preparing a pyripyropene compound
    129.
    发明专利
    Method for preparing a pyripyropene compound 未知

    公开(公告)号：AU2014206958A1

    公开(公告)日：2015-08-06

    申请号：AU2014206958

    申请日：2014-01-15

    Applicant: BASF SE

    Inventor： BONNEKESSEL MELANIE ,  REICHERT WOLFGANG ,  HOOCK RALF ,  KAEDING THOMAS ,  KORADIN CHRISTOPHER ,  PLETSCH ANDREAS ,  EHRESMANN MANFRED ,  SCHRODER HARTWIG

    IPC: C07D493/04 ,  A01N43/90

    Abstract: The present invention relates to a method for preparing the pyripyropene compound of the formula (I) which method comprises the following steps: i) subjecting a pyripyropene compound of formula Pyripyropene A to an alkaline hydrolysis to yield a 1,7,11-trideacetylpyripyropene A, ii) reacting 1,7,11-trideacetylpyripyropene A obtained in step i) with cyclopropane carbonyl chloride to yield a raw product containing the pyripyropene compound of formula (I); iii) subjecting the raw product of step ii) to crystallization to yield a crystalline pyripyropene compound of formula (I) and a mother liquor;and iv) recycling the mother liquor or a pyripyropene compound containing fraction thereof to the alkaline hydrolysis of step i).

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