公开(公告)号：AU2006319263A1

公开(公告)日：2007-06-07

申请号：AU2006319263

申请日：2006-11-23

Applicant: BASF SE

Inventor： KEIL MICHAEL ,  MAYER GUIDO ,  RACK MICHAEL ,  LOHR SANDRA ,  PLESCHKE AXEL ,  GEBHARDT JOACHIM ,  SCHMIDT THOMAS ,  WEVERS JAN HENDRIK

IPC: C07C303/38 ,  C07C201/12 ,  C07C205/58 ,  C07C303/40 ,  C07C311/51

Abstract: A process for preparing sulfonamides I where the variables are each as defined in the description, by reacting m-nitrobenzoyl chlorides II with amino sulfones III, under the influence of B equivalents of base IV, wherein, in step a), the amino sulfone III is reacted with B1 equivalents of base IV, and, in step b), the reaction mixture resulting from step a) is reacted with m-nitrobenzoyl chlorides II and B2 equivalents of base IV; where B, B1 and B2 are each as defined in the description.

公开(公告)号：BRPI0818408A2

公开(公告)日：2015-09-15

申请号：BRPI0818408

申请日：2008-10-10

Applicant: BASF SE

Inventor： PLESCHKE AXEL ,  WEVERS JAN HENDRIK ,  GEBHARDT JOACHIM ,  KEIL MICHAEL ,  LÖHR SANDRA ,  SCHMIDT THOMAS

IPC: C07C303/34 ,  C07C307/06 ,  C07D239/54

公开(公告)号：AU2007306271B2

公开(公告)日：2013-09-26

申请号：AU2007306271

申请日：2007-10-12

Applicant: BASF SE

Inventor： ZAGAR CYRILL ,  SEITZ WERNER ,  KEIL MICHAEL ,  SAXELL HEIDI EMILIA ,  MAYER GUIDO ,  GEBHARDT JOACHIM ,  WOLF BERND ,  LOHR SANDRA ,  SIEVERNICH BERND ,  SCHMIDT THOMAS ,  COX GERHARD ,  ERK PETER ,  REINHARD ROBERT ,  MICHEL ALFRED ,  HAMPRECHT GERHARD ,  WEVERS JAN HENDRIK

IPC: C07D239/54 ,  A01N43/48

Abstract: The present invention relates to hydrates of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N-[[methyl-(1-methylethyl)amino]sulphonyl]benzamide. The invention also relates to a method for preparing these hydrates, and to formulations for crop protection which comprise hydrates of the phenyluracil I.

公开(公告)号：AU2006319263B2

公开(公告)日：2012-06-28

申请号：AU2006319263

申请日：2006-11-23

Applicant: BASF SE

Inventor： RACK MICHAEL ,  PLESCHKE AXEL ,  SCHMIDT THOMAS ,  LOHR SANDRA ,  MAYER GUIDO ,  KEIL MICHAEL ,  WEVERS JAN HENDRIK ,  GEBHARDT JOACHIM

IPC: C07C303/38 ,  C07C201/12 ,  C07C205/58 ,  C07C303/40 ,  C07C311/51

Abstract: The invention relates to methods for producing sulfonamides of formula I, wherein the variables have the designations cited in the description, by reacting m-nitro-benzoic acid chlorides of formula II with aminosulfons of formula III, under the influence of B equivalents of base IV. Said method is characterised in that, during step a) the aminosulfon of formula III is reacted with B1 equivalents of base IV, and during step b), the reaction mixture resulting from step a) is reacted with m-nitro-benzoic acid chlorides of formula II and B2 equivalents of base IV; B, B1 and B2 having the designations cited in the description.

公开(公告)号：ES2361206T3

公开(公告)日：2011-06-14

申请号：ES07821246

申请日：2007-10-12

Applicant: BASF SE

Inventor： SCHMIDT THOMAS ,  GEBHARDT JOACHIM ,  LOEHR SANDRA ,  KEIL MICHAEL ,  WEVERS JAN HENDRIK ,  ERK PETER ,  SAXELL HEIDI EMILIA ,  HAMPRECHT GERHARD ,  SEITZ WERNER ,  MAYER GUIDO ,  WOLF BERND ,  COX GERHARD ,  MICHEL ALFRED ,  ZAGAR CYRILL ,  REINHARD ROBERT ,  SIEVERNICH BERND

IPC: C07D239/54 ,  A01N43/48

Abstract: Forma cristalina II de 2-cloro-5-[3,6-dihidro-3-metil-2,6-dioxo-4-(trifluormetil)-1-(2H)-pirimidinil]-4-fluor-N-[[metil-(1metiletil)amino]sulfonil]-benzamida, en la que la porción de solvente en la red cristalina se encuentra por debajo de 10 % molar respecto de 2-Cloro-5-[3,6-dihidro-3-metil-2,6-dioxo-4-(trifluormetil)-1-(2H)-pirimidinil]-4-fluor-N-[[metil-(1metiletil)amino]sulfonil]benzamida.

公开(公告)号：DE502007006624D1

公开(公告)日：2011-04-14

申请号：DE502007006624

申请日：2007-10-12

Applicant: BASF SE

Inventor： SCHMIDT THOMAS ,  GEBHARDT JOACHIM ,  LOEHR SANDRA ,  KEIL MICHAEL ,  WEVERS JAN HENDRIK ,  ERK PETER ,  SAXELL HEIDI EMILIA ,  HAMPRECHT GERHARD ,  SEITZ WERNER ,  MAYER GUIDO ,  WOLF BERND ,  COX GERHARD ,  MICHEL ALFRED ,  ZAGAR CYRILL ,  REINHARD ROBERT ,  SIEVERNICH BERND

IPC: C07D239/54 ,  A01N43/48

公开(公告)号：UA90767C2

公开(公告)日：2010-05-25

申请号：UAA200807261

申请日：2006-10-26

Applicant: BASF SE

Inventor： BRINK MONIKA ,  KNELL MARCUS ,  WEVERS JAN HENDRIK

IPC: C07D213/81 ,  C07D213/79

公开(公告)号：AT460400T

公开(公告)日：2010-03-15

申请号：AT06807578

申请日：2006-10-26

Applicant: BASF SE

Inventor： BRINK MONIKA ,  KNELL MARCUS ,  WEVERS JAN HENDRIK

IPC: C07D213/81 ,  C07D213/79

Abstract: The invention relates to a process for the preparation of pyridylcarboxylic amides and esters I, Formula (I) wherein Hal, X and R1 have the meanings given in claim 1, which comprises the following steps: (a) heating a mixture consisting essentially of trichloromethylpyridine II, Formula (II), wherein Hal has the meaning given, and 1.0 to 1.5 equivalents of concentrated sulfuric acid, characterized in that the trichloromethylpyridine II in a liquid form is added to the concentrated sulfuric acid at a temperature from 110° C. to 160° C.; and (b) reacting the intermediate product obtained in step (a) with an amine or alcohol III, HXR1, wherein X and R1 have the meaning given, optionally in the presence of a solvent and/or a base.

公开(公告)号：ZA200805691B

公开(公告)日：2009-11-25

申请号：ZA200805691

申请日：2008-06-30

Applicant: BASF SE

Inventor： THOMAS SCHMIDT ,  JOACHIM GEBHARDT ,  SANDRA LOEHR ,  MICHAEL KEIL ,  WEVERS JAN HENDRIK ,  MICHAEL RACK ,  GUIDO MAYER ,  AXEL PLESCHKE

IPC: C07C20100101

公开(公告)号：ZA200804849B

公开(公告)日：2009-11-25

申请号：ZA200804849

申请日：2008-06-04

Applicant: BASF SE

Inventor： MARCUS KNELL ,  WEVERS JAN HENDRIK ,  MONIKA BRINK

IPC: C07D20100101

Abstract: The invention relates to a process for the preparation of pyridylcarboxylic amides and esters I, Formula (I) wherein Hal, X and R1 have the meanings given in claim 1, which comprises the following steps: (a) heating a mixture consisting essentially of trichloromethylpyridine II, Formula (II), wherein Hal has the meaning given, and 1.0 to 1.5 equivalents of concentrated sulfuric acid, characterized in that the trichloromethylpyridine II in a liquid form is added to the concentrated sulfuric acid at a temperature from 110° C. to 160° C.; and (b) reacting the intermediate product obtained in step (a) with an amine or alcohol III, HXR1, wherein X and R1 have the meaning given, optionally in the presence of a solvent and/or a base.