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公开(公告)号:ES2169480T3
公开(公告)日:2002-07-01
申请号:ES98306988
申请日:1998-09-01
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07D239/52 , C07D401/12 , C07D403/12 , C07D413/12 , C07D417/12
Abstract: Preparation of an unsymmetrical 4,6-bis(aryloxy)pyrimidine derivatives of formula (I) is new. The process comprises reacting a 4-halo-6-(aryloxy)pyrimidine compound of formula (II) with >=1 molar equivalent of a 1-4C trialkylamine, a 5-14 membered unsaturated heterocyclic amine optionally substituted to 1-3 1-4C alkyl, or 1-4C alkoxy groups in the presence of an aromatic hydrocarbon and/or a halogenated aromatic hydrocarbon solvents, to form an ammonium halide of formula (III), and reacting the ammonium halide with >=1 phenyl compound of formula (IV) and a base. R1, R8 = H or halo; R1, R7 = H halo, CN, NO2 alkyl, haloalkyl, alkoxy, alkylthio, amino, alkylamino, dialkylamino, alkoxyalkyl, haloalkoxyalkyl or alkoxycarbonyl; R2, R6 = H, halo, alkyl, haloalkyl, haloalkoxy, haloalkoxyalkyl, alkoxycarbonyl, haloalkoxycarbonyl, haloalkylsulphinyl, haloalkylsulphonyl, nitro, or cyano; R3, R5 = H, halo, alkyl or alkoxy; and R4 = H, cyano, alkyl, haloalkyl, alkoxy, alkylthio, alkylsulphinyl, or phenyl; provided that >= 1 of R2 and R6 is not H, and that the aryloxy groups are different. Q = R10N(R9)(R11) or substituted heteroaryl groups of formulae (a)-(g). R9, R10, R11 = 1-4C alkyl, or R910 = 5-6 membered ring with 3-5 O, S or NR-14 atoms; R11 = 1-4C alkyl; Z = O, S or NR14; R12, R13 = H, 1-4C alkyl, 1-4C alkoxy; or R12, R13 = 5-6 membered saturated or unsaturated ring optionally interrupted with O, S, or NR14, and optionally substituted with 1-3 1-4C alkyl or 1-4C alkoxy groups; and R14 = 1-4C alkyl.
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公开(公告)号:CA2416039A1
公开(公告)日:2002-01-24
申请号:CA2416039
申请日:2001-07-13
Applicant: BASF AG
Inventor: SINGH BIJAY K , PEDERSEN MARIANNE K , TECLE BERHANE , KAMESWARAN VENKATARAMAN , BIRK IWONA T , ORTH ANN B , SZUCS STEPHEN S
IPC: A01N43/56 , C07D231/20 , C07D231/32 , C07D401/12 , C07D409/12 , G01N33/50 , C12Q1/37
Abstract: This invention relates to a method for identifying compounds that specifical ly inhibit a metabolic target site or pathway in plants. Enzymes which are specifically affected by the method of the invention include plant pyramidin e biosynthetic pathway enzymes, and particularly the enzymes involved in the conversion of orotate to uridine-5'-monophosphate (UMP). Further, the invention relates to a method for control of undesirable monocotyledonous an d dicotyledenous plant species.
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公开(公告)号:DE60014471D1
公开(公告)日:2004-11-11
申请号:DE60014471
申请日:2000-03-06
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07D405/04 , C07C233/66 , C07C233/69 , C07C251/24 , C07C257/02 , C07D207/02 , C07D207/34 , C07D207/42 , C07D409/04
Abstract: There is provided a process for the preparation of 2-aryl-5-(perfluoroalkyl)pyrrole compounds of formula I from N-Ä1-chloro-1-(perfluoroalkyl)methylÜarylimidoyl chloride compounds. The 2-aryl-5-(perfluoroalkyl)pyrrole compounds are useful for the control of insect and acarid pests, and may also be used to prepare other pesticidal arylpyrrole compounds. In addition, the present invention provides compounds which are useful as intermediates in the preparation of arylpyrrole compounds.
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公开(公告)号:MXPA01008188A
公开(公告)日:2003-07-21
申请号:MXPA01008188
申请日:2000-02-14
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07B61/00 , C07C273/18 , C07C275/20 , C07D239/54 , C07D261/20 , C07D265/06 , C07D275/04 , C07D295/215 , C07D413/04 , C07D417/04 , C07D207/02 , C07D263/44
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公开(公告)号:DE69133140T2
公开(公告)日:2003-03-20
申请号:DE69133140
申请日:1991-11-28
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN , DOEHNER ROBERT FRANCIS JR , BARTON JERRY MICHAEL , KUHN DAVID GEORG
IPC: A01N43/36 , A01P7/02 , A01P7/04 , C07C20060101 , C07C231/02 , C07C233/47 , C07C233/51 , C07C255/58 , C07C255/60 , C07C317/14 , C07C317/50 , C07C321/28 , C07C323/09 , C07C323/63 , C07D20060101 , C07D207/22 , C07D207/34 , C07D207/40 , C07D207/416 , C07D207/42 , C07D317/46 , C07D317/48 , C07D317/60 , C07D317/62
Abstract: There are provided important pyrroline and glycine intermediates, methods for the preparation of said intermediates and the use thereof in the manufacture of arylpyrrole insecticidal agents.
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公开(公告)号:HU0201513A2
公开(公告)日:2002-08-28
申请号:HU0201513
申请日:2000-02-14
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07B61/00 , C07D239/54 , C07D261/20 , C07D275/04 , C07D333/64 , C07D417/04
Abstract: An improved process for the preparation of 6-(perfluoroalkyl) uracil compounds having structural formula (I) from urea compounds having structural formula (II).
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公开(公告)号:ES2170785T3
公开(公告)日:2002-08-16
申请号:ES95308298
申请日:1995-11-21
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07D263/48 , A01N43/36 , C07D207/327 , C07D207/335 , C07D207/34 , C07D405/04 , C07D409/04 , C07D413/04
Abstract: Prodn. of 2-aryl-5-perfluoroalkyl-pyrrole-3-carbonitriles of formula (I) comprises reacting a 5-acylamino-4-aryl-2-perfluoroalkyloxazole of formula (II) or a tautomer of (II), with at least 1 molar equiv. of a 2-haloacrylonitrile or 2,-3-dihalopropionitrile in the presence of a base and opt. a solvent. n = 1-8; A = a gp. of formula e.g. (A1): L = H or halo; M,Q = H, halo, CN, NO2,etc.; or adjacent M+Q = OCH2O, OCF2O or CH=CH-CH=CH; R = 1-6C alkyl, 1-6C haloalkyl, COOR1,etc.; R1 = 1-4C alkyl or 1-4C haloalkyl.
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公开(公告)号:DE69802636T2
公开(公告)日:2002-08-01
申请号:DE69802636
申请日:1998-09-01
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07D239/52 , C07D401/12 , C07D403/12 , C07D413/12 , C07D417/12
Abstract: Preparation of an unsymmetrical 4,6-bis(aryloxy)pyrimidine derivatives of formula (I) is new. The process comprises reacting a 4-halo-6-(aryloxy)pyrimidine compound of formula (II) with >=1 molar equivalent of a 1-4C trialkylamine, a 5-14 membered unsaturated heterocyclic amine optionally substituted to 1-3 1-4C alkyl, or 1-4C alkoxy groups in the presence of an aromatic hydrocarbon and/or a halogenated aromatic hydrocarbon solvents, to form an ammonium halide of formula (III), and reacting the ammonium halide with >=1 phenyl compound of formula (IV) and a base. R1, R8 = H or halo; R1, R7 = H halo, CN, NO2 alkyl, haloalkyl, alkoxy, alkylthio, amino, alkylamino, dialkylamino, alkoxyalkyl, haloalkoxyalkyl or alkoxycarbonyl; R2, R6 = H, halo, alkyl, haloalkyl, haloalkoxy, haloalkoxyalkyl, alkoxycarbonyl, haloalkoxycarbonyl, haloalkylsulphinyl, haloalkylsulphonyl, nitro, or cyano; R3, R5 = H, halo, alkyl or alkoxy; and R4 = H, cyano, alkyl, haloalkyl, alkoxy, alkylthio, alkylsulphinyl, or phenyl; provided that >= 1 of R2 and R6 is not H, and that the aryloxy groups are different. Q = R10N(R9)(R11) or substituted heteroaryl groups of formulae (a)-(g). R9, R10, R11 = 1-4C alkyl, or R910 = 5-6 membered ring with 3-5 O, S or NR-14 atoms; R11 = 1-4C alkyl; Z = O, S or NR14; R12, R13 = H, 1-4C alkyl, 1-4C alkoxy; or R12, R13 = 5-6 membered saturated or unsaturated ring optionally interrupted with O, S, or NR14, and optionally substituted with 1-3 1-4C alkyl or 1-4C alkoxy groups; and R14 = 1-4C alkyl.
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公开(公告)号:DE69525021T2
公开(公告)日:2002-07-18
申请号:DE69525021
申请日:1995-11-21
Applicant: BASF AG
Inventor: KAMESWARAN VENKATARAMAN
IPC: C07D263/48 , A01N43/36 , C07D207/327 , C07D207/335 , C07D207/34 , C07D405/04 , C07D409/04 , C07D413/04
Abstract: Prodn. of 2-aryl-5-perfluoroalkyl-pyrrole-3-carbonitriles of formula (I) comprises reacting a 5-acylamino-4-aryl-2-perfluoroalkyloxazole of formula (II) or a tautomer of (II), with at least 1 molar equiv. of a 2-haloacrylonitrile or 2,-3-dihalopropionitrile in the presence of a base and opt. a solvent. n = 1-8; A = a gp. of formula e.g. (A1): L = H or halo; M,Q = H, halo, CN, NO2,etc.; or adjacent M+Q = OCH2O, OCF2O or CH=CH-CH=CH; R = 1-6C alkyl, 1-6C haloalkyl, COOR1,etc.; R1 = 1-4C alkyl or 1-4C haloalkyl.
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公开(公告)号:CZ20012949A3
公开(公告)日:2002-07-17
申请号:CZ20012949
申请日:2000-02-14
Applicant: BASF AG
Inventor: RAMPULLA RICHARD ANTHONY , KAMESWARAN VENKATARAMAN , WEPPLO PETER JOHN
IPC: C07B61/00 , C07D239/54 , C07D261/20 , C07D275/04 , C07D413/04 , C07D417/04 , C07D417/10 , C07D413/10
Abstract: An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having the structural formula I from 2-(N,N-disubstituted)amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds having the structural formula II
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