Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
  • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
  • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
  • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
  • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
  • C07D239/52—Two oxygen atoms
  • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C255/00—Carboxylic acid nitriles
  • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
  • C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
  • C07C255/60—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton at least one of the singly-bound nitrogen atoms being acylated
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
  • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
  • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
  • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
  • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
  • C07D239/52—Two oxygen atoms
  • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
  • C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
  • C07D239/553—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil

Definitions

• the invention relates to a new process for the preparation of substituted cyanophenyluracils, which are known as herbicidally active compounds, new substituted aminoalkenoic acid cyanophenyl amides as intermediates therefor and an inventive process for their preparation.
• the present invention relates to
• R 1 represents optionally substituted alkyl
• R 2 represents hydrogen, halogen or alkyl
• R 3 represents hydrogen or halogen
• R 4 represents amino, halogen or the grouping -N (R 5 ) SO 2 R 6 ,
• R 5 represents hydrogen or alkyl which is optionally substituted
• R 6 represents optionally substituted alkyl, cycloalkyl or aryl
• R 1 , R 2 , R 3 and R 4 have the meanings given above,
• Z 1 and Z 2 are identical or different and represent halogen, alkoxy, aryloxy, imidazolyl or triazolyl, if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, at temperatures between -20 ° C. and + 150 ° C.,
• R 1 represents optionally substituted alkyl
• R ⁇ 2 represents hydrogen, halogen or alkyl
• R represents hydrogen or halogen
• R 4 represents amino, halogen or the grouping -N (R) SO 2 R,
• R stands for hydrogen or for optionally substituted alkyl, alkylcarbonyl, alkylsulfonyl, cycloalkylcarbonyl, cycloalkylsulfonyl, arylcarbonyl or arylsulfonyl and
• R represents in each case optionally substituted alkyl, cycloalkyl or aryl
• R 1, R, R and R have the meanings given above,
• the invention also relates to the new route for the preparation of substituted cyanophenyluracils of the general formula (I), in which the steps generally set out above under (c) and (a) are carried out.
• the invention preferably relates to the preparation of compounds of the formula (I) and new compounds of the formula (II), in each of which
• R 1 represents optionally substituted by fluorine and or chlorine alkyl having 1 to 4 carbon atoms
• R 2 represents hydrogen, fluorine, chlorine, bromine or alkyl having 1 to 4 carbon atoms
• R represents hydrogen, fluorine, chlorine or bromine and R 4 represents amino, fluorine, chlorine or the grouping -N (R 5 ) SO 2 R 6 , in which
• R 5 for hydrogen or for alkyl, alkylcarbonyl or alkylsulfonyl, each optionally substituted by fluorine and / or chlorine, each having 1 to 6 carbon atoms in the alkyl groups, for cycloalkylcarbonyl or cycloalkylsulfonyl, each optionally substituted by fluorine and / or chlorine, each having 3 to 6 Carbon atoms in the cycloalkyl groups, or phenylcarbonyl or phenylsulfonyl optionally substituted by fluorine and / or chlorine, and
• R 6 represents alkyl with 1 to 6 carbon atoms optionally substituted by fluorine and / or chlorine, cycloalkyl with 3 to 6 carbon atoms optionally substituted by fluorine and / or chlorine, or phenyl optionally substituted by fluorine and / or chlorine
• the invention relates in particular to the preparation of compounds of the formula (I) and new compounds of the formula (II), in each of which
• R 1 each represents methyl or ethyl optionally substituted by fluorine and or chlorine
• R 2 represents hydrogen, fluorine, chlorine, bromine, methyl or ethyl
• R represents hydrogen, fluorine or chlorine
• R 4 represents fluorine, chlorine or the grouping -N (R 5 ) SO 2 R 6 , in which
• R represents hydrogen or methyl, ethyl, n- or i-propyl, acetyl, propionyl, methylsulfonyl or ethyl sulfonyl, optionally substituted by fluorine and / or chlorine, for cyclopropylcarbonyl, cyclobutyl optionally substituted by fluorine and / or chlorine carbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl, cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl or cyclohexylsulfonyl, or phenylcarbonyl or phenylsulfonyl optionally substituted by fluorine and / or chlorine, and R 6 for methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl
• Formula (III) provides a general definition of the carbonic acid derivatives to be used as starting materials in process (a) according to the invention for the preparation of compounds of formula (I).
• Z 1 and Z 2 are the same or different and are preferably fluorine, chlorine, bromine, C 1 -C 4 alkoxy, phenoxy, imidazolyl or triazolyl, in particular chlorine, methoxy, ethoxy or phenoxy.
• Formula (IV) provides a general definition of the cyanophenylpyrimidinones to be used as starting materials in process (c) according to the invention for the preparation of compounds of the formula (II).
• R 1 , R 2 , R 3 and R 4 preferably or in particular have those meanings which have already been mentioned above in connection with the description of the compounds of the formula (I) according to the invention preferably or as particularly preferred for R 1 , R 2 , R 3 and R 4 were given.
• the starting materials of the formula (IV) are known and / or can be prepared by known processes (cf. DE 4431218, production examples).
• Process (c) according to the invention is carried out using a basic compound.
• All conventional inorganic or organic bases are suitable as such. These include, for example, alkaline earth metal or alkali metal hydrides, hydroxides, amides, alcoholates, acetates, carbonates or hydrogen carbonates, such as, for example, lithium, sodium, potassium or calcium hydride, sodium or potassium amide, sodium - or potassium methylate, sodium or potassium ethylate, sodium or potassium n- or i-propylate, sodium or potassium t-butoxide, lithium, sodium, potassium, magnesium or calcium hydroxide, Ammonium hydroxide, sodium or potassium acetate, ammonium acetate, sodium, potassium, magnesium or calcium carbonate, sodium or potassium hydrogen carbonate, ammonium carbonate and tertiary amines, such as trimethylamine, triethylamine, tributylamine, N, N-dimethylaniline, pyridine, N-methylpiperidine, N, N-dimethyl
• Alkali metal carbonates e.g. Sodium or potassium carbonate
• alkali metal hydroxides such as e.g. Sodium or potassium hydroxide
• alkali metal alcoholates such as e.g. Sodium or potassium methylate, sodium or potassium ethylate, sodium or potassium t-butoxide are particularly preferably used as basic compounds in process (c) according to the invention.
• Suitable diluents for carrying out process (c) according to the invention are water and organic solvents. These include in particular aliphatic, alicyclic or aromatic, optionally halogenated Hydrocarbons such as gasoline, benzene, toluene, xylene, chlorobenzene, dichlorobenzene, petroleum ether, hexane, cyelohexane, dichloromethane, chloroform, carbon tetrachloride; Ethers such as diethyl ether, diisopropyl ether, dioxane, tetrahydrofuran or ethylene glycol dimethyl or diethyl ether; Ketones, such as acetone, butanone or methyl isobutyl ketone; Nitriles such as acetonitrile, propionitrile or benzonitrile; Amides such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-formanil
• Water or alcohols e.g. Methanol or ethanol are particularly preferably used as diluents in process (c) according to the invention.
• reaction temperatures can be carried out when carrying out the process according to the invention.
• Process (c) can be varied over a wide range. In general, temperatures between -20 ° C and + 100 ° C, preferably between -5 ° C and + 80 ° C, in particular between + 10 ° C and + 60 ° C.
• Process (c) according to the invention is generally carried out under normal pressure. However, it is also possible to carry out process (c) according to the invention under elevated or reduced pressure - generally between 0.1 bar and 10 bar.
• reaction components are generally mixed at room temperature - or, if appropriate, with gentle cooling - and the reaction mixture is stirred at the temperature required in each case until the end of the reaction.
• the products can be worked up and isolated in the customary manner.
• the organic is shaken with water and a practically immiscible organic solvent, such as methylene chloride, with water Phase separated and dried.
• the solvent is distilled off under reduced pressure and the residue is optionally purified by a customary method (for example chromatography, recrystallization).
• the crude product from process (c) can, however, optionally also be used for the reaction according to process (a) without further purification.
• Process (a) according to the invention for the preparation of the compounds of the formula (I) is preferably carried out in the presence of a suitable reaction auxiliary.
• the usual inorganic or organic bases or acid acceptors are generally suitable as reaction auxiliaries. These preferably include alkali metal or alkaline earth metal acetates, amides, carbonates, hydrogen bicarbonates, hydrides, hydroxides or alkanolates, such as, for example, sodium, potassium or calcium acetate, lithium, sodium , Potassium or calcium amide, sodium, potassium or calcium carbonate, sodium, potassium or calcium bicarbonate, lithium, sodium, potassium or calcium hydride, lithium, sodium, potassium or Calcium hydroxide, sodium or potassium methoxide, ethanolate, n- or i-propanolate, n-, i-, s- or t-butanolate; basic organic nitrogen compounds such as trimethylamine, triethylamine, tripropylamine, tributylamine, ethyldiis
• DAB-CO 1,4-diazabicyclo [2,2, 2] octane
• DBN 1,5-diazabicyclo [4,3,0] non-5-ene
• DBU 1,8 diazabicyclo [5,4,0] -undec-7-ene
• Suitable diluents for carrying out process (a) according to the invention are preferably inert organic solvents. These include, in particular, aliphatic, alicyclic or aromatic, optionally halogenated hydrocarbons, such as, for example, gasoline, benzene, toluene, xylene, chlorobenzene, dichlorobenzene, petroleum ether, hexane, cyelohexane, dichloromethane, chloroform, carbon tetrachloride; Ethers, such as diethyl ether, diisopropyl ether,
• Dioxane tetrahydrofuran or ethylene glycol dimethyl or diethyl ether
• Ketones such as acetone, butanone or methyl isobutyl ketone
• Nitriles such as acetonitrile, propionitrile or benzonitrile
• Amides such as N, N-dimethylformamide, NN-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone or hexamethylphosphoric acid triamid
• Esters such as methyl acetate or ethyl acetate, and sulfoxides such as dimethyl sulfoxide.
• reaction temperatures can be varied within a substantial range when carrying out process (a) according to the invention.
• temperatures between -20 ° C and + 150 ° C, preferably between -10 ° C and + 120 ° C, in particular between 0 ° C and 100 ° C.
• Process (a) according to the invention is generally carried out under normal pressure. However, it is also possible to carry out process (a) according to the invention under elevated or reduced pressure - generally between 0.1 bar and 10 bar.
• process (a) generally 1.0 to 5.0 mol, preferably 1.1 to 2.5 mol, of carbonic acid derivative of the formula (III) and. are employed per mol of substituted aminocrotonic acid-cyanophenylamide of the formula (II) optionally 1.0 to 5.0 mol, preferably 1.2 to 2.5 mol, of reaction auxiliaries.
• the reaction is carried out, worked up and isolated according to known methods.
• cyanophenyluracils to be prepared according to the invention are already known as herbicidally active compounds (cf. EP 648749).

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Plural Heterocyclic Compounds (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)

Applications Claiming Priority (3)

Publications (1)

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• 1996
  • 1996-02-08 DE DE19604582A patent/DE19604582A1/de not_active Withdrawn
• 1997
  • 1997-01-27 EP EP97902232A patent/EP0880506A1/de not_active Withdrawn
  • 1997-01-27 WO PCT/EP1997/000353 patent/WO1997029094A1/de not_active Application Discontinuation
  • 1997-01-27 US US09/117,518 patent/US6169182B1/en not_active Expired - Fee Related
  • 1997-01-27 JP JP9528101A patent/JP2000504675A/ja not_active Ceased
  • 1997-01-27 AU AU15953/97A patent/AU1595397A/en not_active Abandoned
  • 1997-01-31 TW TW086101084A patent/TW394762B/zh active
• 1998
  • 1998-07-31 MX MX9806195A patent/MX9806195A/es not_active IP Right Cessation
• 2000
  • 2000-09-14 US US09/661,690 patent/US6262291B1/en not_active Expired - Fee Related

Non-Patent Citations (1)

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