公开(公告)号：UA100677C2

公开(公告)日：2013-01-25

申请号：UAA200904213

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 ,  A01N43/54

Abstract: Данноеизобретениекасаетсякристаллическойформы 2-хлор-5-[3,6-дигидро-3-метил-2,6-диоксо-4-(трифторметил)-1-(2Н)-пиримидинил]-4-фтор-N-[[метил-(1-метилэтил)амино] сульфонил]бензамида, способаегополучения, атакжепрепаратовдлязащитырастений, которыесодержатуказанноесоединение.

公开(公告)号：NZ575890A

公开(公告)日：2011-07-29

申请号：NZ57589007

申请日：2007-10-12

Applicant: BASF SE

Inventor： SCHMIDT THOMAS ,  GEBHARDT JOACHIM ,  LOHR 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: Disclosed is a crystalline form 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 of formula I. Also disclosed is a method for preparing the phenyluracil crystalline form, and formulations for crop protection which comprise the crystalline form.

公开(公告)号：AT500232T

公开(公告)日：2011-03-15

申请号：AT07821246

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: The present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)-amino]sulfonyl]benzamide. The invention also relates to a process for the preparation of this crystalline form and to plant protection formulations which comprise this crystalline form of the phenyluracil.

公开(公告)号：ZA200903230B

公开(公告)日：2010-07-28

申请号：ZA200903230

申请日：2009-05-11

Applicant: BASF SE

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

IPC: A01N20100101 ,  C07D20100101

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]-sulfonyl]benzamide. The invention also relates to a process for the preparation of these hydrates and to plant protection formulations which comprise hydrates of the phenyluracil I.

公开(公告)号：DE59814338D1

公开(公告)日：2009-03-12

申请号：DE59814338

申请日：1998-01-08

Applicant: BASF SE

Inventor： VON DEYN WOLFGANG ,  HILL REGINA LUISE ,  KARDORFF UWE ,  BAUMANN ERNST ,  ENGEL STEFAN ,  MAYER GUIDO ,  WITSCHEL MATTHIAS ,  RACK MICHAEL ,  GOETZ NORBERT ,  GEBHARDT JOACHIM ,  MISSLITZ ULF ,  WALTER HELMUT ,  WESTPHALEN KARL-OTTO ,  OTTEN MARTINA ,  RHEINHEIMER JOACHIM

IPC: C07D277/10 ,  C07D413/10 ,  A01N43/72 ,  A01N43/76 ,  A01N43/78 ,  A01N43/80 ,  C07D231/20 ,  C07D237/00 ,  C07D261/00 ,  C07D261/04 ,  C07D261/20 ,  C07D263/10 ,  C07D273/00 ,  C07D277/20 ,  C07D277/34 ,  C07D291/04 ,  C07D311/00 ,  C07D403/10 ,  C07D417/10 ,  C07D419/10 ,  C07D498/10

Abstract: Benzoyl derivatives of the formula I where the variables have the following meanings: R1, R2 are hydrogen, nitro, halogen, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl or C1-C6-haloalkylsulfonyl; R3 is hydrogen, halogen or alkyl; R4, R5 are hydrogen, halogen, cyano, nitro, alkyl, alkoxy, alkylthio, dialkylamino, phenyl or carbonyl, it being possible for the 6 last-mentioned radicals to be substituted; X is O, S, NR9, CO or CR10R11; Y is O, S, NR12, CO or CR13R14; R15 is pyrazole which is unsubstituted or substituted, linked in the 4-position and has attached to it in the 5-position a hydroxyl or sulfonyloxy radical; and the agriculturally useful salts thereof; processes and intermediates for the preparation of the 3-heterocyclyl-substituted benzoyl derivatives; compositions comprising them; and the use of these derivatives or compositions comprising them for controlling undesirable plants.

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：BRPI0719214B1

公开(公告)日：2016-11-22

申请号：BRPI0719214

申请日：2007-10-12

Applicant: BASF SE

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

IPC: C07D239/54 ,  A01N43/48

公开(公告)号：AU2007306270B2

公开(公告)日：2013-09-26

申请号：AU2007306270

申请日：2007-10-12

Applicant: BASF SE

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

IPC: C07D239/54 ,  A01N43/48

Abstract: The present invention relates to a crystalline form 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 this crystalline form and to formulations for crop protection which comprise this crystalline form of the phenyluracil.

公开(公告)号：UA98291C2

公开(公告)日：2012-04-25

申请号：UAA201101802

申请日：2006-11-23

Applicant: BASF SE

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

IPC: C07C303/40 ,  C07C201/00 ,  C07C205/00 ,  C07C311/00

Abstract: Способполучениясульфонамидовформулы I EMBED ISISServer I, гдезаместителиимеютзначение, приведенныев описании, реакциейхлоридовм-нитробензойнойкислотыформулы II саминосульфонамиформулы III, вприсутствииВ эквивалентовоснованияформулы IV, причемнастадииа) аминосульфоныформулы III реагируютс В1 эквивалентамиоснованияформулы IV, инастадии b) реакционнуюсмесь, полученнуюнастадииа), подвергаютвзаимодействиюс хлоридамим-нитробензойнойкислотыформулы II иВ2 эквивалентамиоснованияформулы IV, гдеВ, В1 иВ2 имеютзначение, приведенныев описании.

公开(公告)号：BRPI0619760A2

公开(公告)日：2012-02-22

申请号：BRPI0619760

申请日：2006-11-23

Applicant: BASF SE

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

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.