Process for the preparation of 2-(5,5-disubstituted-4-oxo-2-imidazolin-2-yl)nicotinic acids and quinoline-3-carboxylic acids

{
  "publication_number": "US4518780A",
  "country": "US",
  "kind": "A",
  "title": "Process for the preparation of 2-(5,5-disubstituted-4-oxo-2-imidazolin-2-yl)nicotinic acids and quinoline-3-carboxylic acids",
  "abstract": "A novel process for the preparation of 2-(5,5-disubstituted-4-oxoor thiono)-2-imidazolin-2-yl)nicotinic acids, quinoline-3-carboxylic acids and benzoic acids by the base-catalyzed cyclization of appropriately substituted 2-carbamoyl nicotinic acids, 3-quinolinecarboxylic, or benzoic acids. The products are useful as herbicides.",
  "claims": [
    "1. A process for the preparation of a 2-(5,5-disubstituted-4-oxo-2-imidazolin-2-yl)nicotinic acid, 3-quinolinecarboxylic acid or benzoic acid of the formula: ##STR33## wherein R 9 is N or CH; R 1 is C 1 -C 4 alkyl; R 2 is C 1 -C 4 alkyl or C 3 -C 6 cycloalkyl; and when R 1 and R 2 are taken together along with the carbon to which they are attached, they may represent C 3 -C 6 cycloalkyl optionally substituted with methyl, and when R 1 and R 2 are not the same, the optical isomers thereof; X is hydrogen, or C 1 -C 4 alkyl, Y is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, trifluoromethyl, trichloromethyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl or phenoxy optionally substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen; Z is hydrogen, C 1 -C 4 alkyl, trifluoromethyl, trichloromethyl, phenyl or phenyl substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen; and when taken together, Y and Z may form a ring in which YZ are represented by the structure: --(CH 2) n --, where n is an integer from 3 to 5, provided that X is hydrogen; or YZ is ##STR34## where L, M, Q and R 7 are each hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl, phenoxy or mono-substituted phenyl or phenoxy where the substituent is C 1 -C 4 alkoxy or halogen; with the proviso that only one of L, M, Q or R 7, may represent a substituent other than hydrogen, halogen, C 1 -C 4 alkyl or C 1 -C 4 alkoxy; comprising, reacting a compound of the structure: ##STR35## wherein R 9, X, Y, Z, W, R 1 and R 2 are as described above, with from 2 to 20 molar equivalents of an aqueous or aqueous alcoholic sodium or potassium hydroxide of a concentration of 10% or greater and from 0 to 10 molar equivalents of 30 to 90% aqueous hydrogen peroxide at a temperature of from 25° to 100° C. and thereafter acidifying the thus-formed reaction mixture to a pH between 2 and 4 with a strong mineral acid to give the formula (I) acid.",
    "2. A process according to claim 1, wherein the base concentration is from 10 to 40% of the total reaction mixture on a weight basis, used in sufficient quantities to provide from two to six molar equivalents of base for each equivalent of acid amidonitrile reactant.",
    "3. A process for the preparation of a compound having the structure: (IA): ##STR36## wherein R 9 is N or CH; R 1 is C 1 -C 4 alkyl; R 2 is C 1 -C 4 alkyl or C 3 -C 6 cycloalkyl; and when R 1 and R 2 are taken together along with the carbon to which they are attached, they may represent C 3 -C 6 cycloalkyl optionally substituted with methyl, and when R 1 and R 2 are not the same, the optical isomers thereof; X is hydrogen, or C 1 -C 4 alkyl, Y is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, trifluoromethyl, trichloromethyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl or phenoxy optionally substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen; Z is hydrogen, C 1 -C 4 alkyl, trifluoromethyl, trichloromethyl, phenyl or phenyl substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen; and when taken together, Y and Z may form a ring in which YZ are represented by the structure: --(CH 2) n --, where n is an integer from 3 to 5, provided that X is hydrogen; or YZ is ##STR37## where L, M, Q and R 7 are each hydrogen, halogen C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl, phenoxy or monosubstituted phenyl or phenoxy where the substituent is C 1 -C 4 alkoxy or halogen; with the proviso that only one of L, M, Q or R 7, may represent a substituent other than hydrogen, halogen, C 1 -C 4 alkyl or C 1 -C 4 alkoxy; comprising, reacting a compound of the formula: ##STR38## with an equivalent amount of a compound of the formula: ##STR39## in the presence of a solvent of diethyl ether, tetrahydrofuran, dimethoxyethane, acetonitrile or a low-boiling halogenated hydrocarbon, at a temperature between 20° and 60° C. under a blanket of nitrogen, to obtain an isomeric mixture of the compounds having the structures (a) and (b): ##STR40## treating the thus-formed reaction product with 2 to 10 moles of aqueous or aqueous C 1 -C 4 alcoholic sodium or potassium hydroxide and 2 to 5 moles of 30 to 90% aqueous hydrogen peroxide per mole of formula (a) and (b) compound, at a temperature of 25° to 110° C., acidifying the thus-formed reaction mixture to a pH between 2 and 4 with hydrochloric acid or sulfuric acid, extracting the acidified reaction mixture with an organic solvent and separating the solvent from the formula (IA) acid product.",
    "4. A process according to claim 1 wherein R 1 is methyl; R 2 is isopropyl; X is hydrogen; Y is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, trifluoromethyl, trichloromethyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl, phenoxy, or phenyl or phenoxy substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen and Z represents hydrogen, C 1 -C 4 alkyl, trifluoromethyl, trichloromethyl, phenyl or phenyl substituted with one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen.",
    "5. A process according to claim 1 wherein R 1 is methyl; R 2 is isopropyl; X is hydrogen and Y and Z are taken together to form a ring in which YZ represents ##STR41## where L, M, Q and R 7 each are hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, difluoromethoxy, diloweralkylamino, C 1 -C 4 alkylthio, nitro, phenyl, phenoxy or substituted phenyl or phenoxy where the substituent is one C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen; with the proviso that only one of L, M, Q or R 7 may represent a substituent other than hydrogen, halogen, C 1 -C 4 alkyl or C 1 -C 4 alkoxy.",
    "6. A process according to claim 1 for the preparation of (+)-2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid.",
    "7. A process according to claim 1 for the preparation of (+)-2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)nicotinic acid.",
    "8. A process according to claim 1 for the preparation of the mixture of compounds 2-(5-isopropyl-5-methyl-4-oxo-2-imidazolinyl-2-yl)-p-toluic acid and 6-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-m-toluic acid."
  ],
  "cpc": [
    "C07D 213/81",
    "C07D 213/82",
    "C07D 215/54",
    "C07D 233/70",
    "C07D 401/04"
  ],
  "assignees": [
    "AMERICAN CYANAMID CO"
  ],
  "filing_date": "1983-05-05",
  "publication_date": "1985-05-21",
  "grant_date": "1985-05-21",
  "priority_date": "1982-05-25",
  "application_number": "US-48940083-A",
  "family_id": "27009527",
  "citations": [
    "US4017510A"
  ]
}