公开(公告)号：UA89546C2

公开(公告)日：2010-02-10

申请号：UAA200801151

申请日：2006-06-30

Applicant: BASF SE

Inventor： SCHMIDT THOMAS ,  PUHL MICHAEL ,  DICKHAUT JOACHIM ,  BASTIAANS HENRICUS MARIA MARTI ,  RACK MICHAEL ,  CULBERTSON DEBORAH L ,  ANSPAUGH DOUGLAS D ,  BRAUN FRANZ-JOSEF ,  BUCCI TONI ,  COTTER HENRY VAN TUYL ,  KUHN DAVID G ,  OLOUMI-SADEGHI HASSAN

IPC: C07D401/04 ,  A01N43/56 ,  A01P5/00 ,  A01P7/00

Abstract: N-ТіоантраніламіднісполукиформулиІ EMBED ISISServer , (I) деА означаєгрупу, вибрануз А1 таА2 EMBED ISISServer , дезміннітаіндексиприймаютьзначення, визначеніу описі, способиодержаннясполукІ, пестициднікомпозиції, яківключаютьсполукиІ, застосуваннясполукІ дляборотьбиз комахами, акаридамиабонематодами, таспособилікування, боротьби, попередженняабозахистутваринвіднашестяабозараженняпаразитамишляхомзастосуваннясполукформулиІ.

公开(公告)号：DE50312258D1

公开(公告)日：2010-02-04

申请号：DE50312258

申请日：2003-05-15

Applicant: BASF SE

Inventor： HAMPRECHT GERHARD ,  PUHL MICHAEL ,  REINHARD ROBERT ,  SAGASSER INGO ,  SCHMIDT THOMAS ,  GOETZ NORBERT ,  ZIERKE THOMAS

IPC: C07C307/02 ,  C07D239/54 ,  C07C303/34 ,  C07C303/38 ,  C07C303/40 ,  C07C307/00 ,  C07C307/06 ,  C07C307/08 ,  C07C307/10 ,  C07D207/48 ,  C07D211/96 ,  C07D239/46 ,  C07D295/26

Abstract: The present invention relates to a process for preparing sulfamoyl halides of primary or secondary amines, comprising the following steps: i) reacting a primary or secondary amine A1 with at least equimolar amounts of SO 3 or an SO 3 source in the presence of at least equimolar amounts of a tertiary amine A2, based in each case on the amine A1, and ii) reacting the reaction mixture obtained in step i) with at least the amount of a phosphorus halide required by the stoichiometry; The invention further relates to a process for preparing sulfonic diamides, comprising the preparation of sulfamoyl halides by means of carrying out steps i) and ii) and subsequently reacting the sulfamoyl halide obtained with ammonia. The invention further relates to the use of this process for preparing active herbicidal ingredients having a sulfuric diamide structure. The invention further relates to novel sulfamoyl chlorides.

公开(公告)号：DK1893586T3

公开(公告)日：2009-01-05

申请号：DK06755248

申请日：2006-05-18

Applicant: BASF SE

Inventor： GEBHARDT JOACHIM ,  LOEHR SANDRA ,  KEIL MICHAEL ,  SCHMIDT THOMAS ,  WEVERS JAN HENDRIK ,  ZECH HELMUT ,  HAEBERLE RUDOLF

IPC: C07D239/54

Abstract: The present invention relates to a process for preparing 1-alkyl-3-phenyluracils of the formula I where the variables R1 to R7 are as defined in the description by reacting 3-phenyluracils of the formula II and alkylating agents of the formula III R1-L1  III, with one another, wherein during the entire reaction the pH is kept in a range from 1 to 6 by adding base a little at a time.

公开(公告)号：DE502006001614D1

公开(公告)日：2008-10-30

申请号：DE502006001614

申请日：2006-05-18

Applicant: BASF SE

Inventor： GEBHARDT JOACHIM ,  LOEHR SANDRA ,  KEIL MICHAEL ,  SCHMIDT THOMAS ,  WEVERS JAN HENDRIK ,  ZECH HELMUT ,  HAEBERLE RUDOLF

IPC: C07D239/54

Abstract: The present invention relates to a process for preparing 1-alkyl-3-phenyluracils of the formula I where the variables R1 to R7 are as defined in the description by reacting 3-phenyluracils of the formula II and alkylating agents of the formula III R1-L1  III, with one another, wherein during the entire reaction the pH is kept in a range from 1 to 6 by adding base a little at a time.

公开(公告)号：DE60316982T2

公开(公告)日：2008-07-31

申请号：DE60316982

申请日：2003-11-21

Applicant: BASF SE

Inventor： KORDES MARKUS ,  VON DEYN WOLFGANG ,  HOFMANN MICHAEL ,  SCHMIDT THOMAS ,  STEINER GERD ,  TREACY MICHAEL F ,  VAN TUYL COTTER HENRY ,  CULBERTSON DEBORAH ,  SHIEH HONG-MING

IPC: A01N47/06

Abstract: The present invention relates to the use of compounds of formula (I), wherein R is C1-C8-alkyl, unsubstituted or substituted with 1, 2 or 3 radicals selected from the group consisting of halogen, amino, nitro, cyano, C1-C4-alkenyl, C1-C4-haloalkenyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, 5- to 10-membered heteroaryl containing as ring members 1, 2, 3 or 4 heteroatoms selected from oxygen, sulfur and nitrogen, and phenyl, wherein the heteroaryl and phenyl radicals may be substituted for the control of nematodes, a method for the control of nematodes, and a method for the protection of plants from infestation or attack by nematodes.

公开(公告)号：CA2666196A1

公开(公告)日：2008-04-17

申请号：CA2666196

申请日：2007-10-12

Applicant: BASF SE

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

IPC: C07D239/54 ,  A01N43/48

Abstract: The present invention relates to a crystalline form of 2-chloro-5-[3,6-di hydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N- [[methyl-(1-methylethyl)amino]sulphonyl]benzamide. The invention also relate s to a method for preparing this crystalline form and to formulations for cr op protection which comprise this crystalline form of the phenyluracil.

公开(公告)号：AU2007306270A1

公开(公告)日：2008-04-17

申请号：AU2007306270

申请日：2007-10-12

Applicant: BASF SE

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

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：ES2291735T3

公开(公告)日：2008-03-01

申请号：ES03795837

申请日：2003-11-21

Applicant: BASF SE

Inventor： KORDES MARKUS ,  VON DEYN WOLFGANG ,  HOFMANN MICHAEL ,  SCHMIDT THOMAS ,  STEINER GERD ,  TREACY MICHAEL F

IPC: A01N47/06

Abstract: Uso de compuestos de fórmula I: (Ver fórmula) en la que R es alquilo C1-C8, no substituido o substituido con 1, 2 ó 3 radicales seleccionados del grupo que consiste en halógeno, amino, nitro, ciano, alquenilo C1-C4, haloalquenilo C1-C4, alcoxi C1-C4, haloalcoxi C1-C4, alquiltio C1-C4, heteroarilo de 5 a 10 miembros que contiene como miembros de anillo 1, 2, 3 ó 4 heteroátomos seleccionados de oxígeno, azufre y nitrógeno, y fenilo, en donde los radicales heteroarilo y fenilo pueden estar substituidos con cualquier combinación de 1 a 5 átomos de halógeno, 1 ó 2 grupos ciano, 1 ó 2 grupos nitro, de 1 a 3 grupos alquilo C1-C4, de 1 a 4 grupos haloalquilo C1-C4, de 1 a 3 grupos alcoxi C1-C4 o de 1 a 3 grupos haloalcoxi C1-C4, para el control de nematodos parásitos de plantas.

公开(公告)号：CA2821517A1

公开(公告)日：2007-06-07

申请号：CA2821517

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: C07C201/12 ,  C07C205/57 ,  C07C253/30 ,  C07C255/57

Abstract: The invention relates to a process for preparing fluorinated m-nitrobenzoyl chlorides IIA where R1, R2, R3 and R4 are each hydrogen, halogen, cyano, nitro, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy or C1-C6-haloalkoxy, and at least one of the radicals R1 to R4 is fluorine, by hydrolyzing fluorinated m-nitrobenzotrichlorides wherein the reaction takes places in the presence of a catalyst or in a weakly acidic medium and also at temperatures less than 80°C.

公开(公告)号：CA2821516A1

公开(公告)日：2007-06-07

申请号：CA2821516

申请日：2006-11-23

Applicant: BASF SE

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

IPC: C07C201/12 ,  C07C205/57 ,  C07C253/30 ,  C07C255/57

Abstract: The invention relates to a process for preparing fluorinated m-nitrobenzoyl chlorides IIA where R1, R2, R3 and R4 are each hydrogen, halogen, cyano, nitro, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy or C1-C6-haloalkoxy, and at least one of the R1 to R4 radicals is fluorine, by reacting fluorinated m-nitrobenzoic acids with chlorinating agents, the reaction taking place in the presence of catalytic amounts of a phosphine derivative.