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EP1716120A1 - Amides de phenylalanine substitues par un reste heteroaroyle a activite herbicide. - Google Patents

Amides de phenylalanine substitues par un reste heteroaroyle a activite herbicide.

Info

Publication number
EP1716120A1
EP1716120A1 EP04803998A EP04803998A EP1716120A1 EP 1716120 A1 EP1716120 A1 EP 1716120A1 EP 04803998 A EP04803998 A EP 04803998A EP 04803998 A EP04803998 A EP 04803998A EP 1716120 A1 EP1716120 A1 EP 1716120A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
formula
alkoxy
aminocarbonyl
heteroaroyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04803998A
Other languages
German (de)
English (en)
Inventor
Matthias Witschel
Michael Puhl
Michael Rack
Liliana Parra Rapado
Ulf Misslitz
Cyrill Zagar
Peter Plath
Robert Reinhard
Bernd Sievernich
Rex Liebl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP1716120A1 publication Critical patent/EP1716120A1/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/20—N-Aryl derivatives thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C07D213/82—Amides; Imides in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Definitions

  • the present invention relates to heteroaroyl-substituted phenylalanine amides of the formula I.
  • R 1 , R 2 is hydrogen, hydroxy or CC 6 alkoxy
  • Rr C is Ce-alkyl, CC 4 is cyanoalkyl or C 1 -C 6 -haloalkyl;
  • R 5 * is hydrogen, d-C ⁇ -Al yl. CC 6 -haloalkyl, OR ", SR" or NR ⁇ d R 14 ; R 5 is hydrogen or CC 6 alkyl;
  • R 6 , R 7 are hydrogen, halogen, cyano, CC 6 alkyl, dC 6 -haloalkyl, hydroxy, C 1 -C 6 -alkoxy or CC 6 -haloalkoxy;
  • R 8 , R 9 , R 10 are hydrogen, halogen, cyano, C 1 -C 6 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy or CC 6 -haloalkoxy;
  • R 11, R 12, R 13 is hydrogen, 6 -alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 alkenyl, C 3 -C 6 - Alkinyi, C 3 -C 6 -Halogenaikenyl, C 3 -C 6 haloalkynyl, formyl, CC 6 - alkylcarbonyl, C 3 -C 6 cycloalkylcarbonyl, C 6 -C alkenylcarbonyl, C 2 -C 6 - alkynylcarbonyl, dC 6 alkoxycarbonyl, C 3 -C 6 alkenyloxycarbonyl, C 3 -C 6 - alkynyloxycarbonyl, dC 6 alkylaminocarbonyl, C 3 -C 6 -Alkenylamino- carbonyl, C 3 -C 6 -Alkinylaminocarbonyl, C.-Ce-AIkylsul
  • alkyl, cycloalkyl and alkoxy radicals may be partially or completely halogenated and / or may carry one to three of the following groups: cyano, hydroxy, C 3 -C 6 Cycloalkyl, CC 4 alkoxy, C 1 -C 4 alkylthio, di (C 1 -C 4 alkyl) amino, C 1 -C 6 -cycloyl, hydroxycarbonyl, C 1 -C 4 -alkoxycarbonyl, aminocarbonyl, C 1 -C 4 -alkylaminocarbonyl, di- (CC
  • heterocyclyl (heterocyclyl) -aminocarbonyl, or heterocyclyl-dC 6 -alkylcarbonyl, wherein the phenyl and the heterocyclyl radical of the 17 latter substituents may be partially or fully halogenated and / or may carry one to three of the following groups: nitro, cyano, CC 4- alkyl, dC-haloalkyl, C.-C 4 -alkoxy or CC 4 -haloalkoxy; or SO 2 R 15 ;
  • Alkyl and cycloalkyl radicals may be partially or completely halogenated and / or may carry one to three of the following groups: cyano, hydroxy, C 3 -C 6 -cycloalkyl, C 4 -alkoxy, C 4 -alkylthio, di- (C- C 1 -C 4 alkyl) amino, C 1 -C 4 -alkylcarbonyl, hydroxycarbonyl, C 1 -C 4 -alkoxycarbonyl, aminocarboxylic carbonyl, C.
  • C 6 -alkyl, heterocyclyl or heterocycIyl-C 6 -alkyI where the phenyl and the heterocyclyl radical of the 4 last-mentioned substituents can be partially or completely halogenated and / or can carry one to three of the following groups: nitro, cyano, dC dC -Alky !, 4 haloalkyl, dC 4 alkoxy or CC 4 - haloalkoxy;
  • R 15 C r C 6 alkyl, C is Ce-haloalkyl or phenyl, where the phenyl radical may be partially or fully halogenated and / or may carry one to three of the following groups: d-Ce-alkyl, dC 6 -haloalkyl or CC 6 alkoxy;
  • the invention relates to processes and intermediates for the preparation of compounds of formula I, compositions containing them and the use of these derivatives or agents containing them for controlling harmful plants.
  • WO 01/55146, WO 02/06995 and WO 02/40469 inter alia, describe heterocyclylcarbonyl-substituted phenylalanine amides having pharmaceutical activity.
  • herbicidal agents were found which contain the compounds I and have a very good herbicidal activity.
  • methods for the preparation of these compositions and methods for controlling undesired plant growth with the compounds I have been found.
  • the compounds of the formula I contain two or more chiral centers and are then present as enantiomer or diastereomer mixtures.
  • the invention provides both the pure enantiomers or diastereomers and mixtures thereof.
  • the compounds of the formula I can also be present in the form of their agriculturally useful salts, wherein the type of salt generally does not matter.
  • the salts of those cations or the acid addition salts of those acids into consideration, the cations, or anions, the herbicidal effect of the compounds I do not adversely affect.
  • Alkali metals preferably lithium, sodium and potassium, the alkaline earth metals, preferably calcium and magnesium, and the transition metals, preferably manganese, copper, zinc and iron, and ammonium, where, if desired, one to four hydrogen atoms are replaced by C- 4- alkyl, hydroxy C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-d-d-alkyl, hydroxyC 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropylammonium, tetramethylammonium, tetrabutylammonium, 2- ( 2-hydroxy-eth-1-oxy) eth-1-ylammonium, di (2-hydroxyeth-1-yl) ammonium, trimethylbenzylammonium, furthermore phosphonium ions, s
  • Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate,
  • the organic moieties mentioned for the substituents R 1 -R 19 or as radicals on phenyl or heterocyclic rings represent collective terms for individual lists of the individual group members.
  • All hydrocarbon chains ie all alkyl, alkenyl, alkynyl, cyanoalkyl, haloalkyl , Haloalkenyl, haloalkynyl, alkoxy, haloalkoxy, alkoxyalkyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, alkylamino, alkylaminocarbonyl, alkenylaminocarbonyl, alkynylaminocarbonyl, Alkylsulfonylaminocarbonyl, dialkylaminocarbonyl, N-alkenyl-N-alkylaminocarbonyl, N-alkynyl-N
  • halogenated substituents preferably carry one to five identical or different halogen atoms.
  • the meaning halogen in each case represents fluorine, chlorine, bromine or iodine.
  • C 1 -C 4 -alkylcarbonyl C 1 -C 4 -alkylcarbonyl, as mentioned above, and also, for example, pentylcarbonyl , 1-methylbutylcarbonyl, 2-methylbutylcarbonyl, 3-methylbutylcarbonyl, 2,2-dimethylpropylcarbonyl, 1-ethylpropylcarbonyl, hexylcarbonyl, 1,1-dimethylpropylcarbonyl, 1, 2-dimethylpropylcarbonyI, 1-methylpentylcarbonyl, 2-methylpentylcarbonyl, 3 Methyl ethylpentylcarbonyl, 4-methylpentylcarbonylcarbonyl,
  • C 3 -C 6 -cycloalkyl and the cycloalkyl portions of C 3 -C 6 -cycloalkylcarbonyl monocyclic, saturated hydrocarbon having 3 to 6 ring members, such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl;
  • Pentenyl 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl 2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1, 2-Dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1 - pentenyl, 2-
  • Pentynyl 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3 Methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2- pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-d
  • d-C-cyanoalkyl e.g. Cyanomethyl, 1-cyanoeth-1-yl, 2-cyanoeth-1-yl, 1-cyanoprop-1-yl, 2-cyanoprop-1-yl, 3-cyanoprop-1-yl, 1-cyanoprop-2-yl, 2-cyanoprop-2-yl, 1-cyanobut-1-yl, 2-cyanobut-1-yl, 3-cyanobut-1-yl, 4-cyanobut-1-yl, 1-cyanobut-2-yl, 2 Cyanobut-2-yl, 1-cyanobut-3-yl, 2-cyanobut-3-yl, 1
  • C ⁇ C haloalkyl t called a DC 4 -AIkylrest as mentioned above which is chlorine, bromine and / or iodine partially or fully substituted by fluorine, eg
  • dC 6 -haloalkyl C. C 4 haloalkyl as mentioned above, and also, for example, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl, 6-iodohexyl and dodecafluorohexyl;
  • C 3 -C 6 -haloalkenyl a C 3 -C 6 -alkenyl radical, as mentioned above, which is partially or completely substituted by fluorine, chlorine, bromine and / or iodine, for example 2-chloroprop-2-en-1-yl , 3-chloroprop-2-en-1-yl, 2,3-dichloroprop-2-en-1-yl, 3,3-dichloroprop-2-en-1-yl, 2,3,3-trichloro-2 -en-1-yl, 2,3-dichloro-2-en-1-yl, 2-bromoprop-2-en-1-yl, 3-bromoprop-2-en-1-yl, 2,3-dibromoprop -2-en-1-yl, 3,3- Dibromoprop-2-en-1-yl, 2,3,3-tribromo-2-en-1-yl or 2,3-dibromobut-2-en-1-yl;
  • C 3 -C 6 -haloalkynyl a C 3 -C 6 -alkynyl radical as mentioned above which is partially or completely substituted by fluorine, chlorine, bromine and / or iodine, for example 1,1-difluoro-prop-2-yn 1-yl, 3-iodo-prop-2-yn-1-yl, 4-fluorobut-2-yn-1-yl, 4-chlorobutyl
  • dC 4 -alkoxy eg methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy and 1, 1-dimethylethoxy;
  • C 1 -C 4 -alkoxy as mentioned above, as well as e.g. Pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methoxylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2- Methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy,
  • C 1 -C 4 -haloalkoxy a C 1 -C 4 -alkoxy radical as mentioned above which is partially or completely substituted by fluorine, chlorine, bromine and / or iodine, eg fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy, 2- Chloroethoxy, 2-bromomethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2- fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy, 3-fluoropropoxy, 2-chloropropoxy, 3-
  • C 1 -C 6 -haloalkoxy dC -halogenoalkoxy as mentioned above, and also, for example, 5-fluoropentoxy, 5-chloropentoxy, 5-bromopentoxy, 5-iodopentoxy, undecamluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy, 6-bromohexoxy, 6-iodohexoxy and dodecafluorohexoxy;
  • d-C ⁇ -alkoxy-dd-alkyl by C 6 -alkoxy as mentioned above, and substituted C ⁇ -C4 alkyl, eg methoxymethyl, ethoxymethyl, propoxymethyl,
  • -C 4 - alkoxycarbonyl and di (C ⁇ -C4 alkyl) amino-dC 4 alkoxycarbonyl for example methodological xycarbonyl, ethoxycarbonyl, propoxycarbonyl, 1-methylethoxycarbonyl, butoxycarbonyl, 1-methylpropoxycarbonyl, 2-methylpropoxycarbonyl or 1,1-dimethylethoxycarbonyl;
  • C. C 6 alkoxycarbonyl C 1 -C 4 alkoxycarbonyl as mentioned above, and also, for example, pentoxycarbonyl, 1-methylbutoxycarbonyl, 2-methylbutoxycarbonyl, 3-methylbutoxycarbonyl, 2,2-dimethylpropoxycarbonyl, 1-ethylpropoxycarbonyl, hexoxycarbonyl, 1,1 Dimethylpropoxycarbonyl, 1, 2-dimethylpropoxycarbonyl, 1-methylpentoxycarbonyl, 2-methylpentoxycarbonyl, 3-methylpentoxycarbonyl, 4-methylpentoxycarbonyl, 1,1-dimethylbutoxycarbonyl, 1,2-
  • C 1 -C 4 -alkylthio for example methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio and 1,1-dimethylethylthio;
  • C ⁇ -alkyl eg methylamino, ethylamino, propylamino, 1-methylethylamino, butylamino, 1-methylpropylamino, 2-methylpropylamino, 1,1-dimethylethylamino, pentylamino, 1-methylbutylamino, 2-methylbutylamino, 3-methylbutylamino, 2,2- Dimethylpropylamino, 1-ethylpropylamino, hexylamino, 1,1-dimethylpropylamino, 1, 2-dimethylpropylamino, 1-methylpentylamino, 2-methylpentylamino, 3-methylpentylamino, 4-methylpentylamino, 1,1-dimethylbutylamino,
  • Di (C 1 -C 4 alkyl) amino for example N, N-dimethylamino, N, N-diethylamino, N, N-dipropylamino, N, N -di (1-methylethyl) amino, N, N Dibutylamino, N, N -di (1-methylpropyl) amino, N, N -di (2-methylpropyl) -amino, N, N-di- (1, 1-dimethyl-ethyl) -amino, N-ethyl- N-methylamino, N-methyl-N-propylamino, N -methyl-N- (1-methylethyl) amino, N -butyl-N-methylamino, N -methyl-N- (1-methylpropyl) amino, N -methyl- N- (2-methylpropyl) amino, N- (1, 1-dimethylethyl) -N-methylamino, N-ethyl
  • N Di (C.-C 6 alkyl) amino and the dialkylamino radicals of N- (di-dC 6 - alkylaminoHmino-Ci-Ce-alkyl: di- (C 1 -C 4) -alkyl as mentioned above and: for example N , N-dipentyl-amino, N, N-dihexylamino, N-methyl-N-pentylamino, N-ethyl-N-pentylamino, N-methyl-N-hexylamino and N-ethyl-N-hexylamino; (dd-alkylamino) carbonyl: for example, methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, 1-methylethylaminocarbonyl, butylaminocarbonyl, 1-methylpropylaminocarbonyl, 2-methylpropylaminocarbonyl or 1,1-di
  • Di- (C r C4) alkylaminocarbonyl for example N, N-dimethylaminocarbonyl, N, N-diethyl-aminocarbonyl, N, N-di (1-methylethyl) aminocarbonyl, N, N-dipropylaminocarbonyl, N, N-Dibutyiaminocarbonyl , N, N-di (1-methylpropyl) aminocarbonyl, N, N-di (2-methylpropyl) aminocarbonyl, N, N -di (1,1-dimethylethyl) aminocarbonyl, N-ethyl-N-methylaminocarbonyl, N-methyl-N-propylaminocarbonyl, N-methyl-N- (1-methylethyl) aminocarbonyl, N-butyl-N-methylaminocarbonyl, N-methyl-N- (1-methylethyl) -aminocarbonyl, N-methyl- N
  • (C 1 -C 6 -alkylamino) carbonyl (C 1 -C 4 -alkylamino) carbonyl, as mentioned above, and also, for example, pentylaminocarbonyl, 1-methylbutylaminocarbonyl, 2-methylbutylaminocarbonyl, 3-methylbutylaminocarbonyl, 2,2-dimethylpropylamino carbonyl, 1-ethylpropylaminocarbonyl, hexylaminocarbonyl, 1,1-dimethylpropylaminocarbonyl, 1, 2-dimethylpropylaminocarbonyl, 1-methylpentylaminocarbonyl, 2-methylpentylaminocarbonyl, 3-methylpentylaminocarbonyl, 4-methylpentylaminocarbonyl, 1, 1-dimethylbutylaminocarbonyi, 1, 2
  • Dimethylbutylaminocarbonyl 1,3-dimethylbutylaminocarbonyl, 2,2-dimethylbutylaminocarbonyl, 2,3-dimethylbutylaminocarbonyl, 3,3-dimethylbutylaminocarbonyl, 1-ethylbutylaminocarbonyl, 2-ethylbutylaminocarbonyl, 1, 1, 2-trimethylpropylaminocarbonyl, 1, 2,2- Trimethyl-propylaminocarbonyl, 1-ethyl-1-methylpropylaminocarbonyl or 1-ethyl-2-methylpropylaminocarbonyl; Di- (C 1 -C 6 -alkyl) aminocarbonyl: di- (C 1 -C 4 -alkyl) aminocarbonyl as mentioned above, and also, for example, N-methyl-N-pentylaminocarbonyl, N-methyl-N- (1-methylbutyl) -aminocarbonyl, N-methyl-N- (2
  • Di- (C 1 -C 6 -alkyl) -aminothiocarbonyl eg N, N-dimethylaminothiocarbonyl, N, N-diethylaminothiocarbonyl, N, N-di (1-methylethyl) aminothiocarbonyl, N, N-dipropylaminothiocarbonyl, N, N Dibutylaminothiocarbonyl, N, N -di (1-methylpropyl) -amino-thiocarbonyl, N, N -di (2-methylpropyl) -aminothiocarbonyl, N, N-di- (1, 1-dimethyl-ethyl) -aminothiocarbonyl, N-ethyl-N-methylaminothiocarbonyl, N-methyl-N-propylaminothiocarbonyl, N-methyl-N- (1-methylethyl) -aminothiocarbonyl
  • N-propylaminothiocarbonyl N-ethyl-N- (1-methylethyl) -aminothiocarbonyl, N-butyl-N-ethylaminothiocarbonyl, N-ethyl-
  • N- (1-methylpropyl) -aminothiocarbonyl N-ethyl-N- (2-methylpropyl) -aminothiocarbonyl, N-ethyl-N- (1, 1-dimethylethyl) -aminothiocarbonyl, N- (1-methylethyl) -N- propylaminothiocarbonyl, N-butyl-N-propylaminothiocarbonyl, N-
  • heterocyclyl (heterocyclyl) -aminocarbonyl and heterocyclyl-C .
  • -C 6 -alkylcarbonyl a saturated, partially unsaturated or aromatic 5- or 6-membered heterocyclic ring containing one to four identical or different heteroatoms selected from the group oxygen, sulfur or nitrogen, and be bonded via C or N.
  • N-linked, 5-membered, saturated rings such as: Tetrahydropyrrol-1-yl, tetrahydropyrazol-1-yl, tetrahydroisoxazol-2-yl, tetrahydroisothiazol-2-yl, tetrahydroimidazol-1-yl, tetrahydrooxazol-3-yl, tetrahydrothiazol-3-yl;
  • N-linked, 5-membered, partially unsaturated rings such as: 2,3-dihydro-1H-pyrrol-1-yl, 2,5-dihydro-1H-pyrrol-1-yl, 4,5-dihydro-1 H-pyrazol-1-yl, 2,5-dihydro-1H-pyrazol-1-yl, 2,3-dihydro-1H-pyrazol-1-yl, 2,5-dihydroisoxazol-2-yl, 2,3- Dihydroisoxazol-2-yl, 2,5-dihydroisothiazol-2-yl, 2,3-dihydroisoxazol-2-yl, 4,5-dihydro-1H-imidazol-1-yl, 2,5-dihydro-1H, imidazol-1-yl, 2,3-dihydro-1H-imidazol-1-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrothia
  • Triazolin-1-yl 2,4- ⁇ 3 -triazolin-1-yl, 1, 2,4- ⁇ 1 -triazolin-4-yl;
  • N-linked, 5-membered, aromatic rings such as:
  • N-linked, 6-membered, saturated rings such as:
  • C-linked, 6-membered, partially unsaturated rings such as: 2H-3,4-dihydropyran-6-yl, 2H-3,4-dihydropyran-5-yl, 2H-3,4-dihydropyran-
  • Tetrahydropyridin-1-yl 2,5,6-tetrahydropyridin-5-yl, 1, 2,5,6-tetrahydropyridin-6-yl, 2,3,4,5-tetrahydropyridin-2-yl, 2 , 3,4,5-Tetrahydropyridin-3-yl, 2,3,4,5-tetrahydropyridin-4-yl, 2,3,4,5-tetrahydropyridin-5-yl, 2,3,4,5-tetrahydropyridine 6-yl, 4H-pyran-2-yl, 4H-pyran-3-yl, 4H-pyran-4-yl, 4H-thiopyran-2-yl, 4H-thiopyran-3-yl, 4H-
  • Tetrahydropyrimidin-6-yl 1,2,3,4-tetrahydropyrazino-2-yl, 1,2,3,4-tetrahydropyrazine-5-yl, 1,2,3,4-tetrahydropyrimidin-2-yl, 1, 2,3,4-tetrahydropyrimidin-4-yl, 1,2,3,4-tetrahydropyrimidin-5-yl, 1,2,3,4-tetrahydropyrimidin-6-yl, 2,3-dihydro-1, 4-thiazine-2-yl, 2,3-dihydro-1, 4-thiazine-3-yl, 2,3-dihydro-1,4-thiazin-5-yl, 2,3-dihydro-1, 4 thiazine-6-yl, 2H-
  • N-linked, 6-membered, partially unsaturated rings such as: 1, 2,3,4-tetrahydropyridin-1-yl, 1, 2,5,6-tetrahydropyridin-1-yl, 1, 4-dihydro-pyridin-1 - yl, 1,2-dihydropyridin-1-yl, 2H-5,6-dihydro-1,2-oxazin-2-yl, 2H-5,6-dihydro-1,2-thiazin-2-yl, 2H 3,6-dihydro-1,2-oxazin-2-yl, 2H-3.6-dihydro-1,2-thiazin-2-yl, 2H-3,4-dihydro-1,2-oxazin-2-yl , 2H-3,4-dihydro-1,2-thiazin-2-yl, 2,3,4,5-tetrahydropyridazin-2-yl, 1,2,5,6-tetrahydropyridazin-1-yl, 1,2
  • C-linked 5- or 6-membered heteroaryl having one to four nitrogen atoms, or one to three nitrogen atoms and one oxygen or sulfur atom, or having one oxygen or sulfur atom: for example, via a C atom-linked aromatic 5-membered ring HeterocycIen which in addition to carbon atoms one to four nitrogen atoms, or one to three nitrogen atoms and a sulfur or oxygen atom, or a sulfur or oxygen atom may contain as ring members, for example 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 3-pyrazolyl, 4- Pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazoly
  • -N-heterocyclylaminocarbonyl and heterocyclyl-CrC ⁇ -alkylcarbonyl are preferably unsubstituted or carry one to three halogen atoms and / or one nitro group, one cyano radical and / or one or two methyl, trifluoromethyl, Me - thoxy or Trifluormethoxysubstituenten.
  • variables of the compounds of the formula I have the following meanings, these considered individually and in combination with one another representing particular embodiments of the compounds of the formula I:
  • heteroaroyl-substituted phenylalanine amides of the formula I in which A is C-linked 5-membered heteroaryl having one to four nitrogen atoms, or one to three nitrogen atoms and one oxygen or sulfur atom, or with one oxygen or sulfur atom; particularly preferably 5-membered heteroaryl selected from the group of thienyl, furyl, pyrazolyl, imidazolyl, thiazolyl and oxazolyl; especially preferred 5-membered heteroaryl selected from the group thienyl, furyl, pyrazolyl and imidazolyl; where the heteroaryl radicals mentioned may be partially or fully halogenated and / or 1 to 3 radicals from the group cyano, C ⁇ C 6 alkyl, C 3 -C 6 - cycloalkyl, CC 6 haloalkyl, CC 6 -alkoxy, C ⁇ -C 6 - Haloalkoxy, CC 6 - alk
  • heteroaroyl-substituted phenylatanine amides of the formula I in which
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • a C-linked 5- or 6-membered heteroaryl selected from the group pyrrolyl, thienyl, furyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, tetrazolyl, pyridyl and pyrimidinyl; where the heteroaryl radicals mentioned may be partially or fully halogenated and / or 1 to 3 radicals from the group cyano, CC 6 alkyl, C 3 -C 6 cycloalkyl, C.-C 6 -HalogenaIkyl, CC 6 -alkoxy, C. -C 6 - haloalkoxy, C.
  • -C 6 alkoxy-CrC-alkyl amino, (CC 6 alkyl) amino and di (dC 6 -alkyl) can carry amino; particularly preferably C-linked 5- or 6-membered heteroaryl selected from the group of thienyl, furyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl and pyridyl; where the heteroaryl radicals mentioned may be partially or fully halogenated and / or 1 to 3 radicals from the group Ci-Ce-alkyl, C 3 -C 6 - cycloalkyl, and dC can carry 6 -Haiogenalkyl; particularly preferably C-linked 5-membered heteroaryl selected from the group of thienyl, furyl, pyrazolyl, imidazolyl, thiazolyl and oxazolyl; in which said heteroaryl radicals may be partially halogenated and / or may carry from 1 to 2 radicals selected from the
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • a C-linked 5- or 6-membered heteroaryl selected from the group A1 to A14 with
  • R 16 is hydrogen, CC 6 alkyl, C 3 -C 6 cycloalkyl, CC 6 haloalkyl or d- C 6 alkoxy C C 4 alkyl, more preferably CC -AlkyI 4, C 3 -C 6 cycloalkyl, CC -HaIogenalkyl or -C 4 -alkoxy-CrC alkyl, particularly preferably CC alkyl or CC 4 -HalogenalkyI extremely preferably CC 4 alkyl, very extraordinarily preferably CH 3;
  • R 17 is hydrogen, halogen, C. -C 6 alkyl or C 6 haloalkyl, more preferably hydrogen, alkyl or DC 4 DC 4 - haloalkyl, particularly preferably hydrogen or C- ⁇ -C alkyl, extraordinarily preferably hydrogen;
  • R 18 halogen, C 6 alkyl, dC 6 haloalkyl or C 6 haloalkoxy, more preferably halo, CC 4 alkyl or dC 4 haloalkyl, more preferably halo or C r C 4 -HalogenaIkyl extremely preferably CF 3;
  • R 19 is hydrogen, halogen, C.
  • -C 6 alkyl or C 6 haloalkyl more preferably hydrogen, halogen or -C 4 -haloalkyl, particularly preferably hydrogen or halogen, very preferably hydrogen; and mean; particularly preferably A1, A2, A3, A4, A5, A6, A8 or A9; wherein R 16 to R 19 are defined as mentioned above; most preferably A1, A2, A5 or A6; wherein R 16 to R 19 are defined as mentioned above; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • a 3-PyrazolyI which may be partially or fully halogenated and / or by a 6 alkyl to three radicals from the group consisting of C ⁇ -C, C 3 -C 6 cycloalkyl, C. -C 6 - haloalkyl and d-Ce-alkoxy-C .
  • -d-alkyl may be substituted; more preferably 3-pyrazolyl, which may be partially halogenated and / or by a 6 alkyl to three radicals from the group CC, C 3 -C 6 cycloalkyl, CC 6 - haloalkyl and C ⁇ -C 6 -alkoxy-C 4 C -alkyl may be substituted; particularly preferably 3-pyrazolyl, which may be substituted by one to three radicals from the group CC-alkyl, C 3 -C 6 -cycloalkyl, CC 4 -haloalkyl and C.-d-alkoxy-C 1 -C 4 -alkyl; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • a 4-pyrazolyl which may be partially or fully halogenated and / or by one to three radicals from the group dC 6 alkyl, C 3 -C 6 cycloalkyl, dC 6 - haloalkyl and may be substituted; particularly preferably 4-pyrazolyl, which may be partially halogenated and / or by one to three radicals from the group dC 6 alkyl, C 3 -C 6 -cycloalkyl, dC 6 - haloalkyl and C.-C 6 -alkoxy-dC 4 -alkyl may be substituted; more preferably 4-pyrazolyl, which is substituted by one to three radicals from the group CC 4 alkyl, C 3 -C 4 -alkoxy-C C.- 4 may be alkyl substituted 6 cycloalkyl, CC 4 haloalkyl and dC; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • a C-linked pyrazolyl selected from the group A1a to A4a with
  • R 16 denotes d-Ce-alkyl, C 3 -C 6 -cycloalkyl, C r C 6 -haloalkyl or C r C 6 -alkoxy-C 4 -alkyl, particularly preferably C 4 -Atkyl, C 3 -C 6 cycloalkyl, CC 4 haloalkyl or -C 4 -alkoxy-CrC 4 alkyl, particularly preferably CC alkyl or C 4 haloalkyl, extraordinarily preferably CC 4 alkyl, most preferably CH 3 ;
  • R 17 is hydrogen, halogen, CC 6 -alkyl or C.-C 6 -haloalkyl, particularly preferably hydrogen, CC-alkyl or CC 4 -haloalkyl, particularly preferably hydrogen or C 1 -C -alkyl, very preferably hydrogen; and R 18 is halogen, CC 6 alkyl or C.
  • C6 haloalkyl more preferably halo, dC dC -AlkyI or 4 -HaIogenalkyl, particularly preferably C 4 haloalkyl, preferably CF extremely g; mean; particularly preferably A1a, A2a, or A3a, wherein R 6 to R 18 are defined as mentioned above; Most preference is A1a or A2a, wherein R 6 are defined 18 as mentioned above to R;
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 1 is hydrogen or hydroxy, more preferably hydrogen
  • R 2 is hydrogen; mean.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 3 C.-Ce-Alky! or C.-C 6 -haloalkyl, particularly preferably C 1 -C 6 -alkyl, particularly preferably C 1 -C 4 -alkyl, very preferably CH 3 ; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 4 is hydrogen, C. C 4 alkyl, CC 4 haloalkyl, OR 11 , SR 12 or NR 13 R 14 , more preferably hydrogen, C r C 4 alkyl, OR 11 , SR 12 or NR 13 R 14 , particularly preferably hydrogen or C. C 4 alkyl, very particularly preferably hydrogen, also very particularly preferably C 1 -C 4 alkyl; means.
  • R 4 is hydrogen, C. C 4 alkyl or OR 11 , more preferably dC 4 alkyl or OR 11 , more preferably OR 11 ; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 4 OR 11 , SR 12 or NR 13 R 14 , more preferably OR 11 or SR 12 , particularly preferably OR 11 ; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 5 is hydrogen or CC 4 -alkyl, preferably hydrogen or CH 3 , in particular preferably hydrogen; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 6 is hydrogen, halogen, cyano, CC 6 alkyl, hydroxy or C 6 alkoxy, particularly preferably hydrogen, halogen, cyano or C 6 -alkyl, particularly preferably hydrogen, halogen, cyano or C. C 4 alkyl, most preferably hydrogen, fluorine or CH 3 ; means.
  • heteroaroyl-substituted phenylalanine amides of formula I in which R 7 is hydrogen, halogen, cyano, CC 6 alkyl or C 6 haloalkyl, more preferably hydrogen, halogen, cyano or -C 6 -alkyl, particularly preferably hydrogen Halogen, cyano or CC 4 -alkyl, exceptionally preferably hydrogen, halogen or cyano, very particularly preferably hydrogen, fluorine or chlorine; means.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 8, R 9 and R 10 are each independently hydrogen, halogen, cyano, C. -d-alkyl or -CC 4 -haloalkyl, particularly preferably hydrogen, halogen or cyano, particularly preferably hydrogen, fluorine or chlorine, very preferably hydrogen; mean.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 11, R 12 and R 13 are each independently hydrogen, CC 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C. -AIkylcarbonyl -C 6, C 2 - C 6 alkenylcarbonyl, C 3 -C 6 cycloalkylcarbonyl, dC 6 alkoxycarbonyl, d-C ⁇ - alkylaminocarbonyl, CrC 6 -Alkylsulfonylaminocarbonyl, di- (dC 6 alkyl) - aminocarbonyl, N- (C 1 -C 6 -alkoxy) -N- (C 1 -C 6 alkyl) aminocarbonyl, di- (dC 6 alkyl) - aminothicarbonyl, d-C ⁇ -alkoxyimino-CRCE-alkyl, wherein said Alkyl, cycloalkyl and alkoxy radicals can be partially or completely halogenated and /
  • C 6 -alkylcarbonyl where the phenyl radical of the 6 last-mentioned substituents can be partially or completely halogenated and / or can carry one to three of the following groups: nitro, cyano, C 1 -C 4 -alkyl, CC 4 -haloalkyl, CC 4 - Alkoxy or CC 4 haloalkoxy; or SO 2 R 15 ; particularly preferred are hydrogen, C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 -alkynyl, CC 6 alkylcarbonyl, C 2 -C 6 alkenylcarbonyl, -C 6 alkoxycarbonyl, C.
  • C6 - alkylsulfonylaminocarbonyl di- (C 1 -C 6 alkyl) aminocarbonyl, N- (CC 6 -alkoxy) -N- (C -C 6 alkyl.)
  • Aminocarbonyl or di (CrC 6 alkyl ) aminothiocarbonyl where the alkyl or alkoxy radicals mentioned may be partially or fully halogenated and / or may carry one to three of the following groups: cyano, -C 4 alkoxy, CC 4 alkoxycarbonyl, CC 4 - alkylaminocarbonyl, di- (dC -alkyl) -aminocarbonyl or C 1 -alkylcarbonyloxy; Phenyl-C 1 -C 6 -alkyl, phenylcarbonyl, phenylcarbonyl-C 1 -C 6 -alkyl, phenylsulfonylaminocarbonyl or phen
  • alkyl, cycloalkyl or alkoxy radicals in part may be or fully halogenated and / or may carry one to three of the following groups: cyano, hydroxyl, C 3 -C 6 cycloalkyl, dC 4 - alkoxy, C r C alkylthio, di- (dC alkyl) amino, dC 4 alkylcarbonyl, hydroxycarbonyl, dC 4 alkoxycarbonyl, aminocarbonyl, dC 4 - alkylaminocarbonyl, di- (dC 4 alkyl) aminocarbonyl or dd- alkylcarbonyloxy; or SO 2 R 15 ; mean.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which R 11 and R 13 are each independently hydrogen, CC 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, CC 6 - alkylcarbonyl, C Ce-alkoxycarbonyl, C.
  • alkyl and alkoxy radicals are partially or completely may be halogenated and / or may carry one to three of the following groups: cyano, dC 4 -alkoxy, C.
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 12 is hydrogen, C r C 6 alkylcarbonyl, alkoxycarbonyl CC 6, CC 6 - alkylaminocarbonyl, di- (CC 6 alkyl) aminocarbonyl or N- (C ⁇ -C 6 -alkoxy) -N- (d- C 6 -alkyl) -amino-carbonyl, wherein said alkyl and alkoxy radicals may be partially or completely halogenated and / or may carry one to three of the following groups: cyano or dC 4 -alkoxy; particularly preferably hydrogen, dC 4 -AIkylcarbonyl, CC 4 alkoxycarbonyl, CC alkylaminocarbonyl, di- (dC 4 alkyl) aminocarbonyl or N- (dC - alkoxy) -N- (CC alkyl) aminocarbonyl, wherein said Alkyl, and alkoxy radicals may be partially or completely halogenated and / or may carry one to three of
  • -C 4 -haloalkyl CC - alkoxy or CC -haloalkoxy; particularly preferably hydrogen, CC 6 -alkyl, C 3 -C 6 -alkenyl or C 3 -C 6 -alkynyl, where the 3 radicals mentioned can be partially or completely halogenated and / or can carry one to three of the following groups: Cyano, CC 4 alkoxy, C 1 -C 4 alkoxycarbonyl, C 1 -C 4 -alkylaminocarbonyl, di (dd-alkyl-aminocarbonyl or C 1 -C 4 -alkylcarbonyloxy; or phenyl or phenyl-C 1 -C 4 -alkyl, where the phenyl ring of the latter two substituents partially C.-C nitro, cyano, dC 4 alkyl, 4 haloalkyl, CC 4 - alkoxy or C 4 -Halogen
  • heteroaroyl-substituted phenylalanine amides of the formula I in which
  • R 15 is dCe-AIkyl, CC 6 -haloalkyl or phenyl, where the phenyl radical may be partially or partially halogenated and / or may be substituted by C 4 -alkyl; particularly preferably C 1 -C 4 -alkyl, C 1 -C -haloalkyl or phenyl; especially preferably methyl, trifluoromethyl or phenyl. means.
  • R 1 and R 2 are hydrogen;
  • R 3 is dC 4 -alkyl, more preferably CH 3 ;
  • R 4 is hydrogen, dC 4 alkyl, C r C 4 -Haolgenalkyl, OR 11, SR 12 or NR 13 R 14;
  • R 5 is hydrogen
  • R 6 is hydrogen, halogen, cyano or C 1 -C 4 -alkyl, particularly preferably hydrogen, fluorine or CH 3 ;
  • R 7 is hydrogen, halogen or cyano, particularly preferably hydrogen, fluorine or chlorine;
  • R 8 , R 9 and R 10 independently of one another are hydrogen, fluorine or chlorine, particularly preferably hydrogen;
  • R 11 and R 13 are independently hydrogen, C 1 -C 4 -alkylcarbonyl, C 1 -C 4 -alkylaminocarbonyl, di- (C 2 -C 4 -alkyl) aminocarbonyl, phenylaminocarbonyl, N- (C 1 -C 4 -alkyl) -N- (phenyl) aminocarbonyl , SO 2 CH 3 , SO 2 CF 3 or SO 2 (C 6 H 5 );
  • R 2 is hydrogen, CC 4 alkylcarbonyl, CC 4 alkoxycarbonyl, d -C 4 - alkylaminocarbonyl, di- (dC 4 alkyl) aminocarbonyl, N- (CC 4 -alkoxy) -N- (dC
  • the compounds of the formula Ib in particular the compounds of the formulas Ib 1 to Ib 630, which differ from the corresponding compounds of the formulas Ia1 to Ia630 in that R 16 is CH 2 CH 3 .
  • the compounds of the formula Ic in particular the compounds of the formula Ic1 to Ic630, which differ from the corresponding compounds of the formula Ia1 to Ia630 in that R 16 is CH 2 CF 3 .
  • the compounds of the formula Ip in particular the compounds of the formulas Ipl to Ip630, which differ from the corresponding compounds of the formulas Ia1 to Ia630 in that A for A 3 comprises stands.
  • heteroaroyl-substituted phenylalanine amides of the formula I can be obtained in various ways, for example by the following processes:
  • a phenylalanine of the formula V is first reacted with heteroaryl acid (derivatives) of the formula IV to give the corresponding heteroaroyl derivative of the formula III, which subsequently reacts with an amine of the formula II to give the desired heteroaroyl-substituted phenylalanine amide of the formula I: V III
  • L 1 is a nucleophilically displaceable leaving group, for example for hydroxy or d-Ce-alkoxy.
  • L 2 is a nucleophilically displaceable leaving group, for example, hydroxy, halogen, d-Ce-alkylcarbonyl, C.-Ce-alkoxycarbonyl, -CC 4 -alkylsulfonyl, phosphoryl or isoureyl.
  • Suitable activating reagents are condensing agents such as, for example, polystyrene-bonded dicyclohexylcarbodiimide, diisopropylcarbodiimide, carbonyldiimidazole, chlorocarbonic acid esters such as methyl chloroformate, ethyl chloroformate, isophoryl chloroformate, isobutyl chloroformate, sec-butyl chloroformate or allyl chloroformate, pivaloyl chloride, Polyphosphoric acid, propanephosphonic anhydride, bis (2-oxo-3-oxazolidinyl) - phosphoryl chloride (BOPCI) or sulfonyl chlorides such as methanesulfonyl chloride, toluenesulfonyl chloride or benzenesulfonyl chloride.
  • condensing agents such as, for example, polystyrene-bonded dicyclohexylcar
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether , Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran (THF), nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert.
  • aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene
  • halogenated hydrocarbons such
  • DMF dimethylformamide
  • DMA dimethylacetamide
  • NMP N-methylpyrrolidone
  • Suitable bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and Calcium hydride, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal bicarbonates such as sodium bicarbonate, also organic bases, eg tertiary amines such as trimethylamine, triethylamine, diisopropylethylamine, N-methylmorpholine, and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration. Particularly preferred are sodium hydroxide, triethyl
  • the bases are generally used in equimolar amounts. But they can also be used in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use IV in an excess relative to V.
  • reaction mixtures are worked up in customary manner, for example by mixing with water, separation of the phases and optionally chromatographic purification of the crude products.
  • the intermediate and end products fall z. T. in the form of viscous oils, which are freed or purified under reduced pressure and at moderately elevated temperature of volatile fractions. If the intermediate and final products are obtained as solids, the purification can also by recrystallization or Diggering done.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether , Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran (THF), nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert.
  • aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene
  • halogenated hydrocarbons such
  • Bases generally include inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal bicarbonates such as sodium bicarbonate, as well as organic bases, eg tertiary amines such as trimethylamine, triethylamine, diisopropylethylamine, N-methylmorpholine, and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration. Particularly preferred are sodium hydroxide, triethy
  • the bases are generally used in equimolar amounts. But they can also be used in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use IV in an excess relative to V.
  • the phenylalanines of the formula V can first be reacted with amines of the formula II to give the corresponding amines, which then react with heteroaryl acid (derivatives) n of the formula IV to give the desired heteroaroyl-substituted phenylalanine amides of the formula I.
  • R 4 OR 11 : by condensation of glycinenolate equivalents with benzaldehydes (Hvidt, T. et al., Tetrahedron Lett 27 (33), 3807-3810 (1986); Saeed, A. et al., Tetrahedron 48 (12 ), 2507-2514 (1992); Kikuchi, J. et al., Chem. Lett. (3), 553-556 (1993); Soloshonok, VA et al., Tetrahedron Lett. 35 (17), 2713-2716 (1994); Soloshonok, VA; et al.; Tetrahedron 52 (1), 245-254 (1996); Rozenberg, V. et al., Angew. Chem.
  • R 4 SR 12 : by cleavage of 2-acylamino-3-thioalkyl-phenylalanine derivatives (Villeneuve, G. et al., J. Chem. Soc. Perkin Trans. 1 (16), 1897-1904 (1993)) by ring-opening of Thiazolidinethiones (Cook, AH et al., J. Chem. Soc. 1337 (1948).)
  • R 4 NR 13 R 14 : by ring opening of substituted imidazolinones (Kavrakova, IK et al., Org. Prep. Proced. Int. 28 (3), 333-338 (1996)) by ring-opening of substituted imidazolines (Meyer R. , Liebigs Ann. Chem., 1183 (1977); Hayashi, T. et al., Tetrahedron Lett. 37 (28), 4969-4972 (1996); Lin, YR et al., J. Org. Chem. 6), 1799-1803 (1997); Zhou, XT et al., Tatrahedron Assym.
  • R 4 OR 11 : by condensation of glycinenolate equivalents with aldehydes: Nicolaou, KC et al., J. Am. Chem. Soc. 124 (35), 10451-10455 (2002); Carrara, G. et al., Gazz. Chim. Ital. 82, 325 (1952); Fuganti, C. et al., J. Org. Chem. 51 (7), 1126-1128 (1986); Boger, D.L. et al., J. Org. Chem. 62 (14), 4721-4736 (1997); Honig, H. et al., Tetrahedron (46), 3841 (1990); Kanemasa, S.
  • R 4 SR 12 : by ring opening of substituted thiazolidines (Nagai, U. et al., Heterocycles 28 (2), 589-592 (1989)) by ring opening of substituted aziridines with thiols (Legters, J. et al., Recl. Trav. Chim. Pays-Bas 111 (1), 16-21 (1992))
  • R 4 NR 13 R 14 : by reduction of substituted 2-azido-3-amino-phenylalanine derivatives (Lee SH, Tetrahedron 57 (11), 2139-2145 (2001)) by ring opening of substituted imidazolines (Zhou, XT et al., Tetrahedron Asymmetr. 10 (5), 855-862 (1999); Hayashi, T. et al., Tetrahedron Lett. 37 (28), 4969-4972 (1996))
  • heteroaryl acid (derivatives) of the formula IV required for the preparation of the heteroaroyl derivatives of the formula III can be purchased or can be prepared analogously to the rules known from the literature via a Grignard reaction from the corresponding halide [e.g. A. Mannschuk et. AI, Angew. Chem. 100, 299 (1988)].
  • Suitable activating reagents are condensing agents, e.g. polystyrene-bonded dicyclohexylcarbodiimide, diisopropylcarbodiimide, carbonyldiimidazole, chlorocarbonic acid esters such as methyl chloroformate, ethyl chloroformate, isoropyl chloroformate, isobutyl chloroformate, sec-butyl chloroformate or allyl chloroformate, pivaloyl chloride, polyphosphoric acid, propanephosphonic anhydride, bis (2-oxo-3-oxazolidinyl) phosphoryl chloride (BOPCI) or sulfonyl chlorides such as methanesulfonyl chloride, toluene sul - Fonyl chloride or benzenesulfonyl chloride.
  • condensing agents e.g. polystyrene-bonded dicyclohexyl
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether , Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran (THF), nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butyl Butan
  • Suitable bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and Calcium hydride, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal bicarbonates such as sodium bicarbonate, also organic bases, for example tertiary amines such as trimethylamine, triethylamine, Dtisopropylethylamin, N-methylmorpholine, and N-methylpiperidine, pyridine, substituted pyridines such as collidine Lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration. Particularly preferred
  • the bases are generally used in catalytic amounts, but they can also be used equimolar, in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use II in an excess relative to III.
  • the workup and isolation of the products can be done in a conventional manner.
  • Amides of formula I is usually carried out at temperatures of 0 ° C to the boiling point of the reaction mixture, preferably 0 ° C to 100 ° C, more preferably at room temperature in an inert organic solvent, optionally in the presence of a base [cf. Kawahata, N.H. et al., Tetrahedron Lett. 43 (40), 7221-7223 (2002); Takahashi, K. et al., J. Org. Chem. 50 (18), 3414-3415 (1985); Lee, Y. et al., J. Am. Chem. Soc. 121 (36), 8407-8408 (1999)].
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as benzene, toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether , Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran (THF), nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butyl Butan
  • the reaction may optionally be carried out in the presence of a base.
  • bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal hydrogen carbonates such as sodium bicarbonate, as well as organic bases, eg tertiary amines such as trimethylamine, triethylamine, diisopropylethylamine, N-methylmorpholine, and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-
  • Dimethylaminopyridine and bicyclic amines into consideration are particularly preferred.
  • Particularly preferred are sodium hydroxide, triethylamine, ethyldiisopropylamine, N-methylmorpholine and pyridine.
  • the bases are generally used in catalytic amounts, but they can also be used equimolar, in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use II in an excess relative to III.
  • the workup and isolation of the products can be done in a conventional manner.
  • the amines of the formula II required for the preparation of the heteroaroyl-substituted serine amides of the formula I can be purchased.
  • VIIIb L 1 is a nucleophilically displaceable leaving group, for example for hydroxy or dC 6 - alkoxy.
  • L 2 is a nucleophilically displaceable leaving group, for example for hydroxy, halogen, d-Ce-alkylcarbonyl, CC 6 -alkoxycarbonyl, CC 4 -alkylsulfonyl, phosphoryl or isoureyl.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, Anisole and tetrahydrofuran, and dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably diethyl ether, dioxane and tetrahydrofuran.
  • aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes
  • aromatic hydrocarbons such as toluene, o-, m- and p-xylene
  • ethers such as die
  • Suitable bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal azides such as lithium hexamethyldisilazide, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyllithium, and also alkali metal and alkaline earth metal alcoholates such as sodium methoxide, sodium methoxide.
  • alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride
  • alkali metal azides such as lithium hexamethyldisilazide
  • organometallic compounds in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyllithium
  • alkali metal and alkaline earth metal alcoholates such as sodium methoxide, sodium methoxide.
  • Potassium ethoxide, potassium tert-butoxide, potassium tert-pentoxide and Dimethoxymagnesium also organic bases, eg tertiary amines such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines such as collidine, lutidine and 4-dimethylaminopyridine and bicyclic amines into consideration.
  • Particularly preferred are sodium hydride, lithium hexamethyldisilazide and lithium diisopropylamide.
  • the bases are generally used in equimolar amounts, but they can also be used catalytically, in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use the base and / or the heterocyclylcarbonyl compounds VII in an excess based on the glycine derivatives VIII.
  • the workup and isolation of the products can be done in a conventional manner.
  • the glycine derivatives of the formula VIII required for the preparation of the compounds I can be purchased, are known in the literature [z. H. Pessoa-Mahana et al., Synth. Comm. 32, 1437 (2002) or can be prepared according to the cited literature.
  • L 1 is a nucleophilically displaceable leaving group, for example for hydroxy or dC 6 - alkoxy.
  • L 3 is a nucleophilically displaceable leaving group, for example halogen, hydroxy, or d-Ce-alkoxy.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propinonitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-rButylmethylketon, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert .-Butano
  • Suitable bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal hydrogencarbonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyllithium, alkylmagnesium halides such as methylmagnesium chloride and alkali metal and alkaline earth metal alkoxides such Sodium methoxide, sodium ethoxide, potassium,
  • the bases are generally used in equimolar amounts, but they can also be used catalytically, in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use the base and / or IX in an excess based on IM or I.
  • the workup and isolation of the products can be done in a conventional manner.
  • the required compounds of formula VIII can be purchased.
  • L 1 is a nucleophilically displaceable leaving group, for example for hydroxy or dC 6 - alkoxy.
  • L 2 is a nucleophilically displaceable leaving group, for example hydroxy, halogen, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -alkylsulfonyl, phosphoryl or isopropyl.
  • L 4 represents a nucleophilic displaceable leaving group, for example for hydroxy or -CC 6 - alkoxy.
  • the formula X is usually carried out analogously to the reaction of the phenylalanines of the formula V mentioned under process A with heteroaryl acid (derivatives) n of the formula IV to give the corresponding heteroaroyl derivatives of the formula III.
  • L 4 in the case of the N-acylaminomalonyl compounds of the formula X is C 1 -C 6 -oxy, it is advantageous to first prepare L 4 by ester hydrolysis [eg Hellmann, H. et al., Liebigs Ann. Chem. 631, 175-179 (1960)] into a hydroxy group.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 -alkanes, aromatic hydrocarbons such as toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, Diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butyl Butanol and tert-butan
  • Suitable bases are generally inorganic compounds such as alkali metal and alkaline earth metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides such as lithium oxide, sodium oxide, calcium oxide and magnesium oxide, alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, Alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, potassium carbonate and calcium carbonate and alkali metal hydrogencarbonates such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls such as methyllithium, butyl lithium and phenyllithium, alkylmagnesium halides such as methylmagnesium chloride and alkali metal and alkaline earth metal alkoxides such Sodium methoxide, sodium ethoxide, potassium,
  • the bases are generally used in catalytic amounts, but they can also be used equimolar, in excess or optionally as a solvent.
  • the starting materials are generally reacted with one another in equimolar amounts. It may be advantageous to use the base in an excess based on X.
  • the workup and isolation of the products can be done in a conventional manner.
  • the required aminomalonyl compounds of the formula XI can be purchased or are known in the literature [z. US 4904674; Hellmann, H. et al., Liebigs Ann. Chem. 631, 175-179 (1960)] or can be prepared according to the cited literature.
  • the required heterocyclic compounds of formula VII can be purchased.
  • L 1 is a nucleophilically displaceable leaving group, for example for hydroxy or dC 6 - alkoxy.
  • L 2 is a nucleophilically displaceable leaving group, for example hydroxyl, halogen, d-Ce-alkylcarbonyl, C. -Ce-alkoxycarbonyl, dC 6 -alkylsulfonyl, phosphoryl or isopropyl.
  • acylation of the keto compounds of the formula XIII with heteroaryl acid (derivatives) n of the formula IV to N-acyl keto compounds of the formula XII is usually carried out analogously to the reaction of the phenylalanines of the formula V with heteroaryl acid (derivatives) n of the formula IV mentioned in process A. corresponding heteroaroyl derivatives of the formula IM.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of C 5 -C 8 alkanes, aromatic hydrocarbons such as Toluene, o-, m- and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone , Diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and
  • Suitable reducing agents are e.g. Sodium borohydride, zinc borohydride, sodium cyanoborohydride, lithium triethylborohydride (Superhydrid®), lithium tri-sec.butylborohydride (L-Selectrid®), lithium aluminum hydride or borane [cf. e.g. WO 00/20424; Marchi, C. et al., Tetrahedron 58 (28), 5699 (2002); Blank, S. et al., Liebigs Ann. Chem. (8), 889-896 (1993); Kuwano, R. et al., J. Org. Chem. 63 (10), 3499-3503 (1998); Clariana, J. et al., Tetrahedron 55 (23), 7331-7344 (1999)].
  • the reduction can also be carried out in the presence of hydrogen and a catalyst.
  • Suitable catalysts are, for. B. [Ru (BINAP) CI 2 ] or Pd / C [see. Noyori, R. et al., J. Am. Chem. Soc. 111 (25), 9134-9135 (1989); Bolhofer, A. et al., J. Am. Chem. Soc. 75, 4469 (1953)].
  • the reduction can also take place the presence of a microorganism.
  • a microorganism e.g. Saccharomyces Rouxii [cf. Soukup, M. et al., Helv. Chim. Acta 70, 232 (1987)].
  • N-acyl keto compounds of the formula XII and the respective reducing agent are generally reacted with one another in equimolar amounts. It may be advantageous to use the reducing agent in an excess relative to XII.
  • the workup and isolation of the products can be done in a conventional manner.
  • A, R 1 and R 4 to R 10 are as defined in claim 1 and L is a nucleophilically displaceable leaving group, for example for hydroxy or dC 6 - alkoxy, are also an object of the present invention.
  • a 5- or 6-membered heteroaryl selected from the group of thienyl, furyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl and pyridyl; wherein said heteroaryl may be partially or fully halogenated and / or may carry from 1 to 3 of dC 6 alkyl, C 3 -C 6 cycloalkyl, and dC 6 haloalkyl;
  • R 1 is hydrogen
  • R 4 is hydrogen, CC 4 alkyl, C r C 4 haloalkyl, OR 11 , SR 12 or NR 13 R 14 ;
  • R 5 is hydrogen;
  • R 6 is hydrogen, fluorine or CH 3 ;
  • R 7 is hydrogen, fluorine or chlorine
  • R 8 , R 9 and R 10 are hydrogen;
  • R 11 and R 13 are independently hydrogen, dC alkylcarbonyl, dC 4 - alkylaminocarbonyl, di- (dC 4 alkyl) aminocarbonyl, phenylaminocarbonyl, N- (C1 -C4 -alkyl) -N- (phenyl) aminocarbonyl, SO 2 CH 3 or SO 2 (C 6 H 5 );
  • R 12 is hydrogen, CC 4 alkylcarbonyl, dC 4 alkylaminocarbonyl, di- (dC 4 - alkyl) aminocarbonyl, phenylaminocarbonyl, N- (C r C 4 -alkyl) -N- (phenyl) - aminocarbonyl; and R 14 is hydrogen or C 1 -C -alkyl.
  • heteroaroyl derivatives of the formula III in which A C-linked pyrazolyl selected from the group A1 to A4 with
  • R 17 is hydrogen, halogen, C 1 -C 6 -alkyl or C 1 -C 6 -haloalkyl; particularly preferably hydrogen, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl; especially preferably hydrogen or C 1 -C 4 -alkyl; most preferably hydrogen; and
  • R 18 is halogen, CC 6 alkyl or CC 6 haloalkyl; particularly preferably halogen, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl; particularly preferably CC 4 -haloalkyl; most preferably CF 3 ; particularly preferably A1a, A2a, or A3a, wherein R 16 to R 18 are defined as mentioned above; Most preference is A1a or A2a, wherein R 6 are defined 18 as mentioned above to R;
  • R 1 is hydrogen
  • R 4 is hydrogen, CC 4 alkyl, CC 4 haloalkyl, OR 11 , SR 12 or NR 13 R 14 ;
  • R 5 is hydrogen
  • R 6 is hydrogen, fluorine or CH 3 ;
  • R 7 is hydrogen, fluorine or chlorine;
  • R 8 , R 9 and R 10 are hydrogen;
  • R 1 and R 13 are independently hydrogen, dC 4 alkylcarbonyl, C. -C 4 -alkylaminocarbonyl, di- (CC-alkyl) -aminocarbonyl, phenylaminocarbonyl, N- (C 1 -C 4 -alkyl) -N- (phenyl) -aminocarbonyl, SO 2 CH 3 or SO 2 (C 6 H 5 ) ; .12 hydrogen, dC 4 alkylcarbonyl, C ⁇ -C 4 alkylaminocarbonyl, di- (CC 4 - alkyl) aminocarbonyl, phenylaminocarbonyl, N- (dC alkyl) -N- (phenyl) - aminocarbonyl; and
  • R 1 ' 4 4 is hydrogen or CC 4 alkyl
  • the pyrazolylcarbonyl-substituted phenylalanine amides of the formula I and their agriculturally useful salts are suitable - both as mixtures of isomers and in the form of pure isomers - as herbicides.
  • the compounds of the formula I containing herbicidal agents control plant growth on non-crop areas very well, especially at high application rates. In crops such as wheat, rice, corn, soybeans and cotton, they act against weeds and grass weeds without significantly damaging the crops. This effect occurs especially at low application rates.
  • the compounds of the formula I or herbicidal compositions containing them can be used in a further number of crop plants for the removal of unwanted plants.
  • the following cultures may be considered:
  • the compounds of formula I may also be used in cultures tolerant to the action of herbicides by breeding, including genetic engineering.
  • the compounds of formula I or the herbicidal compositions containing them for example, in the form of directly sprayable aqueous solutions, powders, suspensions, even high-percentage aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, scattering agents or Gra - nulaten be applied by spraying, atomizing, dusting, scattering or pouring.
  • the forms of application depend on the intended use; In any case, they should ensure the finest possible distribution of the active compounds according to the invention.
  • the herbicidal compositions contain a herbicidally effective amount of at least one compound of the formula I or an agriculturally useful salt of I and auxiliaries customary for the formulation of crop protection agents.
  • Suitable inert auxiliaries are essentially:
  • Medium to high boiling mineral oil fractions such as kerosene and diesel oil, coal tar oils and vegetable or animal oils, aliphatic, cyclic and aromatic hydrocarbons, e.g. Paraffins, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone, strong polar solvents, e.g. Amines such as N-methylpyrrolidone and water.
  • mineral oil fractions such as kerosene and diesel oil, coal tar oils and vegetable or animal oils, aliphatic, cyclic and aromatic hydrocarbons, e.g. Paraffins, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols
  • Aqueous application forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water.
  • the substrates as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agents, tackifiers, dispersants or emulsifiers.
  • concentrates consisting of active substance, wetting, adhesion, dispersing or emulsifying agent and possibly solvent or oil, which are suitable for dilution with water.
  • Suitable surface-active substances are the alkali metal, alkaline earth metal, ammonium salts of aromatic sulfonic acids, for example lignin, phenol, naphthalene and dibutylnaphthalenesulfonic acid, and of fatty acids, alkyl and alkylaryl sulfonates, alkyl, lauryl ether and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols and also of fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and its derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethyl tocylphenol ether, ethoxylated isooctyl, octyl or nonylphenol , Alkyl tocylphenol
  • Granules e.g. Coating, impregnation and homogeneous granules can be prepared by binding the active compounds to solid carriers.
  • Solid carriers are mineral soils such as silicic acids, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bolus, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, Ureas and vegetable products such as cereal flour, tree bark, wood and nut shell flour, cellulose powder or other solid carriers.
  • the concentrations of the compounds of the formula I in the ready-to-use formulations can be varied within wide limits.
  • the formulations contain from about 0.001 to 98 wt .-%, preferably 0.01 to 95 wt .-%, of at least one active ingredient.
  • the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • the application of the compounds of the formula I or of the herbicidal compositions can be carried out in the preemergence or postemergence process. If the active ingredients are less compatible with certain crops, application techniques may be used in which the herbicidal agents are sprayed with the help of the sprayers so as not to hit the leaves of the sensitive crops, while the active ingredients on the leaves below grow undesirable plants or the uncovered soil surface (post-directed, lay-by).
  • the application rates of compound of the formula I depending on the control target, season, target plants and growth stage from 0.001 to 3.0, preferably 0.01 to 1, 0 kg / ha of active substance (aS).
  • the pyrazolylcarbonyl-substituted phenylalanine amides of the formula I can be mixed with numerous representatives of other herbicidal or growth-regulating active ingredient groups and applied together.
  • the culture vessels used were plastic flower pots with loamy sand with about 3.0% humus as substrate.
  • the seeds of the test plants were sown separately by species.
  • the active ingredients suspended or emulsified in water were applied directly after sowing by means of finely distributing nozzles.
  • the jars were lightly rained to promote germination and growth and then covered with clear plastic hoods until the plants had grown. This cover causes a uniform germination of the test plants, if it was not affected by the active ingredients.
  • test plants were grown depending on the growth form only to a stature height of 3 to 15 cm and only then treated with the suspended or emulsified in water agents.
  • the test plants were either sown directly and grown in the same containers or they were first grown separately as seedlings and transplanted into the test containers a few days before the treatment.
  • the application rate for postemergence treatment was 0.5, 0.25, 0.125 and 0.0625 kg / ha a.s. (active substance).
  • the plants were kept species-specific at temperatures of 10 to 25 ° C and 20 to 35 ° C.
  • the trial period lasted for 2 to 4 weeks. During this time, the plants were cared for, and their response to each treatment was evaluated.
  • the rating was based on a scale of 0 to 100. 100 means no emergence of the plants or complete destruction of at least the above-ground parts and 0 no damage or normal growth course.
  • the plants used in the greenhouse experiments were composed of the following species:

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
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  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Furan Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Pyrrole Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

La présente invention concerne des amides de phénylalanine à substituant hétéroaroyle de formule (I) dans laquelle A représente un hétéroaryle à liaison carbone, et leurs sels qui peuvent être employés en agriculture. L'invention a également pour objet des procédés et des produits intermédiaires pour les produire, ainsi que l'utilisation de ces composés ou d'agents contenant ces composés, pour lutter contre des végétaux indésirables.
EP04803998A 2003-12-19 2004-12-17 Amides de phenylalanine substitues par un reste heteroaroyle a activite herbicide. Withdrawn EP1716120A1 (fr)

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DE10360463 2003-12-19
PCT/EP2004/014391 WO2005061464A1 (fr) 2003-12-19 2004-12-17 Amides de phenylalanine a substituant heteroaroyle herbicides

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AU (1) AU2004303491A1 (fr)
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CA (1) CA2548354A1 (fr)
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PE (1) PE20051057A1 (fr)
UA (1) UA81567C2 (fr)
UY (1) UY28680A1 (fr)
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UY28680A1 (es) 2005-08-31
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AU2004303491A1 (en) 2005-07-07
US20070060480A1 (en) 2007-03-15
MXPA06005991A (es) 2006-08-23
PE20051057A1 (es) 2006-01-17
CN1898213A (zh) 2007-01-17
KR20060111582A (ko) 2006-10-27
EA011928B1 (ru) 2009-06-30
UA81567C2 (en) 2008-01-10
BRPI0417813A (pt) 2007-03-27
EA200601095A1 (ru) 2007-02-27
ZA200605925B (en) 2008-06-25
CA2548354A1 (fr) 2005-07-07
IL175883A0 (en) 2006-10-05
JP2007514692A (ja) 2007-06-07
CR8476A (es) 2006-12-07
AR046792A1 (es) 2005-12-21

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