91.
    发明专利
    未知

    公开(公告)号:DE502006001074D1

    公开(公告)日:2008-08-21

    申请号:DE502006001074

    申请日:2006-02-14

    Applicant: BASF SE

    Abstract: 5-Alkoxyalkyl-6-alkyl-7-aminoazolopyrimidines of the formula I in which the substituents are defined as follows: R 1 is alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, cyanoalkyl, and benzyloxyalkyl, where the groups in the aliphatic or aromatic moiety may be unsubstituted or may have substitution by from one to three groups R a : R a is halogen, cyano, nitro, hydroxy, cycloalkyl, alkoxy, alkylthio, and NR A R B ; R A , R B are hydrogen and alkyl; R 2 is alkoxyalkyl, phenoxyalkyl, alkylthioalkyl, and phenylthioalkyl, which groups may have no substitution or may have substitution according to the description; R 3 is hydrogen and alkyl; A is N and C-R A ; processes for preparation of these compounds, compositions comprising them, and their use for controlling phytopathogenic harmful fungi.

    92.
    发明专利
    未知

    公开(公告)号:AT400576T

    公开(公告)日:2008-07-15

    申请号:AT06708259

    申请日:2006-02-14

    Applicant: BASF SE

    Abstract: 5-Alkoxyalkyl-6-alkyl-7-aminoazolopyrimidines of the formula I in which the substituents are defined as follows: R 1 is alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, cyanoalkyl, and benzyloxyalkyl, where the groups in the aliphatic or aromatic moiety may be unsubstituted or may have substitution by from one to three groups R a : R a is halogen, cyano, nitro, hydroxy, cycloalkyl, alkoxy, alkylthio, and NR A R B ; R A , R B are hydrogen and alkyl; R 2 is alkoxyalkyl, phenoxyalkyl, alkylthioalkyl, and phenylthioalkyl, which groups may have no substitution or may have substitution according to the description; R 3 is hydrogen and alkyl; A is N and C-R A ; processes for preparation of these compounds, compositions comprising them, and their use for controlling phytopathogenic harmful fungi.

    93.
    发明专利
    未知

    公开(公告)号:AT388152T

    公开(公告)日:2008-03-15

    申请号:AT04803851

    申请日:2004-12-14

    Applicant: BASF SE

    Abstract: 6-(2-Halo-4-alkoxyphenyl)triazolopyrimidines of the formula I in which the substituents are as defined below: R 1 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 contains one to four heteroatoms from the group consisting of O, N and S, R 2 is hydrogen or one of the groups mentioned under R 1 , 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 one to three further heteroatoms from the group consisting of O, N and S as ring members; R 3 is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, phenylalkyl, mono- or dialkoxyalkyl; R 1 , R 2 and/or R 3 may be substituted as mentioned in the description; L is hydrogen, fluorine or chlorine; X is cyano, alkyl, alkoxy, alkenyloxy, haloalkoxy or haloalkenyloxy; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

    Process for preparing substituted biphenyls

    公开(公告)号:AU2007267055A1

    公开(公告)日:2007-12-06

    申请号:AU2007267055

    申请日:2007-05-31

    Applicant: BASF SE

    Abstract: A process for preparing substituted biphenyls of the formula I in which the substituents are defined as follows: X is fluorine or chlorine; R1 is nitro, amino or NHR3; R2 is cyano, nitro, halogen, C1-C6-alkyl, C1-C-6-alkenyl, C1-C6-alkynyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-alkylcarbonyl or phenyl; R3 is C1-C4-alkyl, C1-C4-alkenyl or C1-C4-alkynyl; n is 1, 2 or 3, where in case that n is 2 or 3, the R.sup.2 radicals may also be different, which comprises reacting the compound of the formula II in which Hal is halogen and X and R1 are as defined above, in the presence of a base and of a palladium catalyst selected from the group of:3 a) palladium-triarylphosphine or -trialkylphosphine complex with palladium in the zero oxidation state, b) salt of palladium in the presence of triarylphospine or trialkylphosphine as a complex ligand or c) metallic palladium, optionally applied to support, in the presence of triarylphosphine or trialkylphosphine, in a solvent, with a diphenylborinic acid (III) in which R2 and n are as defined above, where the triarylphosphines or trialkylphosphines used may be substituted.

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