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公开(公告)号:DE50100541D1
公开(公告)日:2003-10-02
申请号:DE50100541
申请日:2001-06-21
Applicant: BASF AG
Inventor: GYPSER DR , GROTE DR , RHEINHEIMER DR , ROSE DR , CULLMANN DR , GEWEHR DR , GRAMMENOS DR , TORMO I BLASCO DR , MUELLER DR , SAUTER DR , AMMERMANN DR , STRATHMANN DR , LORENZ DR , STIERL DR
IPC: C07C251/80 , A01N33/26 , A01N37/50 , C07C249/16 , C07C251/86
Abstract: Hydrazonomethyl-salicylic acid (I) derivatives are new. The hydrazonomethyl-salicylic acid derivatives are compounds of formula (I). X = halo, NO2, CN, 1-4C alkyl, or 1-4C alkoxy; m = 0-3; A = OH, 1-4C alkoxy, NH2, NHCH3, or N(CH3)2; R = phenyl, naphthyl, 3-10C cycloalkyl, 5- or 6-membered heteroaryl or heterocyclyl containing 1-3 N and/or 1 O or S or 1 or 2 O and/or S (each optionally substituted with 1-3 Ra); Ra = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, phenyl, phenoxy, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, C(=NOR alpha )-OR beta , or OC(R alpha )2-C(R beta )=NOR beta , and cyclic groups are optionally substituted with 1-3 Rb; Rb = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C cycloalkenyl, phenyl, phenoxy, phenylthio, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, or C(=NOR alpha )-OR beta ; R alpha and R beta = H or 1-6C alkyl; R = H, CN, or 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl, 1-6C haloalkyl, 1-6C alkoxy or 1-6C alkylthio (each optionally substituted with 1 or more halo and/or 1-3 Rc); Rc = halo, CN, NO2, OH; 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo); 1-6C alkylcarbonyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 2-6C alkenyl, 3-6C alkenyloxy, 3-6C alkynyloxy, or 1-4C alkylenedioxy (optionally halogenated). An Independent claim is also included for the preparation of compounds (I).
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公开(公告)号:DE59409830D1
公开(公告)日:2001-09-20
申请号:DE59409830
申请日:1994-10-04
Applicant: BASF AG
Inventor: GRAMMENOS DR , KIRSTGEN DR , KOENIG DR , OBERDORF DR , SAUTER DR , LORENZ DR , AMMERMANN DR
IPC: A01N37/38 , A01N37/42 , A01N37/44 , A01N37/50 , A01N43/40 , A01N43/54 , A01N43/60 , A01N43/66 , A01N43/707 , A01N43/76 , A01N43/78 , A01N43/82 , C07C69/738 , C07C251/42 , C07C251/48 , C07D213/79 , C07D239/34 , C07D239/52 , C07D241/18 , C07D285/13 , C07D333/32
Abstract: Naphthyl ethers of the formula I in which the index and the substituents have the following meaning: A is optionally substituted phenyl or optionally substituted 5- to 6-membered heteroaryl which, in addition to carbon ring members, can contain one to three nitrogen atoms or one or two nitrogen atoms and an oxygen or sulphur atom or an oxygen or sulphur atom as further ring members; n is 0 or 1; X is oxygen, sulphur or nitrogen, the nitrogen atom carrying one of the following radicals: hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C3-C6-cycloalkyl, optionally substituted phenyl or optionally substituted benzyl; Y is oxygen or in the case where Z is NOCH3: oxygen or nitrogen, where the nitrogen atom carries one of the following radicals: hydrogen, C1-C4-alkyl or C1-C4-alkoxy; Z is CHOCH3, NOCH3, CHCH3 or CHCH2CH3; R is C1-C4-alkyl; R is optionally substituted C1-C6-alkyl, C3-C6-cycloalkyl, C2-C6-alkenyl or C3-C6-alkynyl; optionally substituted phenyl; optionally substituted 5- or 6-membered heteroaryl containing, in addition to carbon ring members, one to three nitrogen atoms or one or two nitrogen atoms and an oxygen or sulphur atom as further ring members; or in the case where the value of n is 0 additionally to the above meanings: halogen, C1-C6-alkoxy, C1-C4-alkylsulphoxyl or phenylsulphoxyl, where the phenyl ring can in turn carry substituents, process for the preparation of the naphthyl ethers I, compositions containing them and their use for the control of animal pests or harmful fungi.
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公开(公告)号:DE50200390D1
公开(公告)日:2004-06-03
申请号:DE50200390
申请日:2002-10-18
Applicant: BASF AG
Inventor: ROSE DR , TORMO I BLASCO DR , GEWEHR DR , GRAMMENOS DR , MUELLER DR , RHEINHEIMER DR , SCHAEFER DR , SCHIEWECK DR , GROTE DR , GYPSER DR , AMMERMANN DR , LORENZ DR , STIERL DR , STRATHMANN DR , CARTER DR , CURTZE DR
IPC: A01N31/14 , A01N31/16 , A01N33/10 , A01N37/38 , A01N37/40 , C07B61/00 , C07C39/42 , C07C41/26 , C07C43/23 , C07C69/017 , C07C69/14 , C07C323/19 , C07C323/25
Abstract: Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives (I) are new. Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives of formula (I) are new: X = O or S; R , R = halo, CN, NO2, OH, SH, NH2, alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylcarbonyloxy, OCHO, alkylthio, alkenylthio, alkynylthio, mono- or dialkylamino, alkylcarbonyl or CHO (where all hydrocarbyl moieties are optionally mono- or polyhalogenated); R = halo, CN, NO2, OH, SH, NH2, alkyl, alkoxy, haloalkyl or haloalkoxy; R = alkyl, alkenyl or alkynyl (all optionally mono- or polyhalogenated); R , R = OH, alkyl, alkenyl, haloalkyl, haloalkenyl, alkoxy, alkenyloxy, haloalkoxy, haloalkenyloxy, cycloalkyl, cycloalkyl-(1-3C) alkyl, cycloalkoxy or cycloalkyl-(1-3C) alkoxy; and n = 0-2. Unless specified otherwise alkyl moieties have 1-6C, alkenyl or alkynyl moieties 2-6C and cycloalkyl moieties 3-8C. An Independent claim is also included for the preparation of (I).
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公开(公告)号:DE59410323D1
公开(公告)日:2003-10-16
申请号:DE59410323
申请日:1994-02-12
Applicant: BASF AG
Inventor: KIRSTGEN DR , GRAMMENOS DR , BAYER DR , DOETZER DR , KOENIG DR , OBERDORF DR , SAUTER DR , WINGERT DR , LORENZ DR , AMMERMANN DR , HARRIES DR
IPC: C07C251/48 , A01N37/50 , A01N43/50 , A01N43/56 , A01N43/647 , A01N43/653 , A01N43/74 , A01N43/76 , A01N43/78 , A01N43/80 , A01N43/82 , A01N43/824 , A01N43/828 , A01N43/836 , A01P3/00 , A01P7/02 , A01P7/04 , C07D207/00 , C07D231/18 , C07D231/20 , C07D231/22 , C07D233/70 , C07D233/84 , C07D249/04 , C07D249/08 , C07D249/12 , C07D261/12 , C07D263/20 , C07D263/38 , C07D263/40 , C07D263/46 , C07D271/06 , C07D271/07 , C07D271/10 , C07D271/113 , C07D277/20 , C07D277/28 , C07D277/34 , C07D277/36 , C07D285/08 , C07D285/125 , C07D401/04 , C07D403/04 , C07D405/04 , C07D409/04 , C07D413/04 , C07D417/04 , C07D417/14
Abstract: Ortho-substd. 2-methoxyiminophenyl ethanoic acid methyl amide derivs. of formula (I) are new. In (I), n = 0-4, X = O or S, Y = 5-membered heteroaromatic ring, which in addn. to R2 can also contain up to 3 gps. chosen from Cl, Me, CF3 or OMe, each R1 is NO2, CN, halogen, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio opt. substd. Ph or PhO. R2 = H, opt. substd. alkyl, alkenyl or alkynyl, on opt. substd. satd. or mono- or di-unsatd. ring contg. in addn. to C, 1-3 heteroatoms as ring members chosen from O, S and N or an opt. substd. mono- or di-nuclear aromatic ring contg. in addn. to C, 1-4 N or 1-2 N and 1 O or S heteroatoms as ring members.
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