USRE39607E1 - Herbicidal sulphonylamino(thio) carbonyl compounds - Google Patents

Herbicidal sulphonylamino(thio) carbonyl compounds Download PDF

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USRE39607E1
USRE39607E1 US10/603,997 US60399703A USRE39607E US RE39607 E1 USRE39607 E1 US RE39607E1 US 60399703 A US60399703 A US 60399703A US RE39607 E USRE39607 E US RE39607E
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chloro
substituted
case optionally
cyano
methoxy
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Klaus-Helmut Müller
Rolf Kirsten
Ernst Rudolf F. Gesing
Joachim Kluth
Mark Wilhelm Drewes
Kurt Findeisen
Johannes Rudolf Jansen
Klaus König
Hans-Jochem Riebel
Otto Schallner
Markus Dollinger
Hans-Joachim Santel
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Bayer AG
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole 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
    • 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
    • A01N43/72—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
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • 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
    • A01N43/72—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
    • A01N43/82—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 three ring hetero atoms
    • 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<
    • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C249/04—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
    • C07C249/12—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes by reactions not involving the formation of oxyimino groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/78—Halides of sulfonic acids
    • C07C309/86—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/87—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/65—N-sulfonylisocyanates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
    • C07C331/16—Isothiocyanates
    • C07C331/32—Isothiocyanates having isothiocyanate groups acylated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/12—Oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/14—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole 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
    • C07D263/36—One oxygen atom
    • C07D263/42—One oxygen atom attached in position 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Definitions

  • the invention relates to novel sulphonylamino(thio) carbonyl compounds, to a number of processes and to novel intermediates for their preparation, and to their use as herbicides.
  • certain sulphonylaminocarbonyl compounds such as, for example, the compounds 4,5-dimethoxy-2-(2-methoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl-1H-pyrazole-3-carboxamide possess herbicidal properties (cf. EP 341489, EP 422469, EP 425948, EP 431291, EP 5071
  • novel sulphonylamino(thio)carbonyl compounds of the general formula (I) are obtained if (a) aminosulphonyl compounds of the general formula (II) in which
  • novel sulphonylamino(thio)carbonyl compounds of the general formula (I) are distinguished by a strong herbicidal activity.
  • the invention relates preferably to compounds of the formula (I) in which
  • the invention also relates preferably to sodium, potassium, magnesium, calcium, ammonium, C 1 -C 4 -alkyl-ammonium, di-(C 1 -C 4 -alkyl)-ammonium, tri-(C 1 -C 4 -alkyl)-ammonium, tetra-(C 1 -C 4 -alkyl)-ammonium, tri-(C 1 -C 4 -alkyl)-sulphonium, C 5 - or C 6 -cycloalkyl-ammonium and di-(C 1 -C 2 -alkyl)-benzyl-ammonium salts
  • the invention relates in particular to compounds of the formula (I) in which
  • a very particularly preferred group of compounds according to the invention are the compounds of the formula (I), in which
  • radical definitions listed above apply not only to the end products of the formula (I) but also, correspondingly, to the starting materials and/or intermediates required in each case of the preparation. These radical definitions can be combined as desired with one another, thus including combinations between the preferred ranges indicated.
  • a general definition of the aminosulphonyl compounds to be used as starting materials in the process (a) according to the invention for the preparation of compounds of the formula (I) is given by the formula (II).
  • R 1 and R 2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or, respectively, particularly preferable for A, R 1 and R 2 .
  • the starting materials of the formula (II) are known and/or can be prepared by methods known per se (cf. EP 216504, DE 3208189, EP 44807, EP 23422).
  • the starting materials of the formula (II) can in general be obtained also by reacting phenol derivatives of the formula (IIb) in which
  • phenol derivatives of the formula (IIb) required as precursors are known and/or can be prepared by methods known per se (cf. EP 44807, Metalloberflache [Metal surface]—Angew. Elektrochemie 27 (1973), 217-227—cited in Chem. Abstracts 79:86733; Preparation Examples).
  • alkylating agents of the formula (XI) which are also required as precursors are known synthesis chemicals.
  • a general definition of the (thio)carboxylic acid derivatives also to be used as starting materials in the process (a) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (III).
  • Q and R 3 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or, respectively, particularly preferable for Q and R 3 ;
  • Z preferably represents fluorine, chlorine, bromine, C 1 -C 4 -alkoxy, phenoxy or benzyloxy, and in particular represents chlorine, methoxy, ethoxy or phenoxy.
  • the starting materials of the formula (III) are known and/or can be prepared by methods known per se (cf. EP 459244, EP 341489, EP 422469, EP 425948, EP 431291, EP 507171, EP 534266).
  • a general definition of the sulphonyl iso(thio)cyanate to be used as starting materials in the process (b) according to the invention for the preparation of the compounds of the formula (I) is given with the formula (IV).
  • A, Q, R 1 and R 2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, Q, R 1 and R 2 .
  • the starting materials of the formula (IV) are known and/or can be prepared by methods known per se (cf. EP 23422, EP 216504).
  • novel sulphonyl iso(thio)cyanates of the formula (IVa) are obtained if sulphonamides of the formula (IIa)—above—are reacted with phosgene or, respectively, thiophosgene, optionally in the presence of an alkyl isocyanate, for example butyl isocyanate, optionally in the presence of a reaction auxiliary, for example diazabicyclo [2.2.2]octane, and in the presence of a diluent, for example toluene, xylene or chlorobenzene, at temperatures between 80° C. and 150° C., and, after the end of the reaction, the volatile components are distilled off under reduced pressure.
  • an alkyl isocyanate for example butyl isocyanate
  • a reaction auxiliary for example diazabicyclo [2.2.2]octane
  • a diluent for example toluene, xylene or chlorobenzene
  • R 3 preferably or in particular has that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for R 3 .
  • the starting materials of the formula (V) are known and/or can be prepared by methods known per se (cf. EP 341489, EP 422469, EP 425948, EP 431291, EP 507171, EP 534266).
  • a general definition of the chlorosulphonyl compounds to be used as starting materials in the processes (c) and (d) according to the invention for the preparation of compounds of the formula (I) is given by the formula (VI).
  • A, R 1 and R 2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, R 1 and R 2 .
  • the starting materials of the formula (VI) are known and/or can be prepared by methods known per se (cf. EP 511826, DE 3208189, EP23422).
  • aniline derivatives of the formula (XII) required as precursors are known and/or can be prepared by methods known per se (cf. EP 511826, US 4992091, EP 185128, DE 2405479, Preparation Examples).
  • the starting materials of the formula (VIII) are known and/or can be prepared by methods known per se (cf. EP 459244).
  • a general definition of the sulphonylamino(thio)carbonyl compounds to be used as starting materials in the process (e) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (IX).
  • A, Q, R 1 and R 2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, Q, R 1 and R 2 ;
  • Z preferably represents fluoro, chloro, bromo, C 1 -C 4 -alkoxy, phenoxy or benzyloxy, and in particular represents chlorine, methoxy, ethoxy or phenoxy.
  • a general definition of the benzene derivatives to be used as starting materials in the process (f) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (X).
  • A, R 1 and R 2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, R 1 and R 2 .
  • aliphatic and aromatic, optionally halogenated hydrocarbons such as pentane, hexane, heptane, cyclohexane, petroleum ether, benzine, ligroin, benzene, toluene, xylene, methylene chloride, ethylene chloride, chloroform, tetrachloromethane, chlorobenzene and o-dichlorobenzene; ethers such as diethyl ether and dibutyl ether, glycol dimethyl ether and diglycol dimethyl ether, tetrahydrofuran and dioxanes; ketones such as acetone, methyl ethyl ketone, methyl isopropyl ketone and methyl isobutyl ketone; esters such as methyl acetate and ethyl acetate; nitrites, for example acetonitrile and propionitrile; amides, for example pentane
  • reaction auxiliaries and/or as acid acceptors in the processes (a), (b), (c), (d), (e) and (f) according to the invention it is possible to employ all acid-binding agents which can customarily be used for such reactions.
  • suitable examples are alkali metal hydroxides, for example sodium, hydroxide and potassium hydroxide, alkaline earth metal hydroxides, for example calcium hydroxide, alkali metal carbonates and alcoholates, such as sodium carbonate and potassium carbonate, sodium tert-butylate and potassium tert-butylate, and also basic nitrogen compounds such as trimethylamine, triethylamine, tripropylamine, tributylamine, diisobutylamine, dicyclohexylamine, ethyldiisopropylamine, ethyldicyclohexylamine, N,N-dimethylbenzylamine, N,N-dimethyl-aniline, pyridine, 2-methyl-, 3-methyl-, 4-methyl
  • reaction temperatures in the processes (a), (b), (c), (d), (e) and (f) according to the invention can be varied within a relatively wide range. They are in general carried out at temperatures of between ⁇ 20° C. and +150° C., preferably at temperatures between 0° C. and +100° C.
  • the starting materials required in each case are in general employed in approximately equimolar quantities. However, it is also possible to use one of the components employed in each case in a relatively large excess.
  • the reactions are in general carried out in a suitable diluent in the presence of an acid acceptor, and the reaction mixture is stirred for a number of hours at the particular temperature required.
  • Working up in the case of the processes (a), (b), (c), (d), (e) and (f) according to the invention is in each case by customary methods (cf. the Preparation Examples).
  • Salts of the compounds of the general formula (I) according to the invention can be prepared if desired. Such salts are obtained in a simple manner by customary methods of forming salts, for example by dissolving or dispersing a compound of the formula (I) in an appropriate solvent, for example methylene chloride, acetone, tert-butyl methyl ether or toluene, and adding an appropriate base. The salts can then—if desired after prolonged stirring—be isolated by concentration or filtration with suction.
  • an appropriate solvent for example methylene chloride, acetone, tert-butyl methyl ether or toluene
  • the active compounds according to the invention can be used as defoliants, desiccants, agents for destroying broad-leaved plants and, especially, as weed-killers.
  • weeds in the broadest sense, there are to be understood all plants which grow in locations where they are not wanted. Whether the substances according to the invention act as total or selective herbicides depends essentially on the amount used.
  • the active compounds according to the invention can be used, for example, in connection with the following plants:
  • the compounds are suitable, depending on the concentration, for the total combating of weeds, for example on industrial terrain and rail tracks, and on paths and squares with or without tree plantings. Equally, the compounds can be employed for combating weeds in perennial cultures, for example afforestations, decorative tree plantings, orchards, vineyards, citrus groves, nut orchards, banana plantations, coffee plantations, tea plantations, rubber plantations, oil palm plantations, cocoa plantations, soft fruit plantings and hopfields, in lawns, turf and pasture-land, and for the selective combating of weeds in annual cultures.
  • the compounds of the formula (I) according to the invention are preferably suitable for combating monoctyledon and dicotyledon broad-leaved weeds, both pre-emergence and post-emergence. They exhibit strong herbicidal activity and a broad spectrum action when used on the soil and on above-ground parts of the plants.
  • the active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusting agents, pastes, soluble powders, granules, suspension-emulsion concentrates, natural and synthetic materials impregnated with active compound, and very fine capsules in polymeric substances.
  • formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surface-active agents, that is emulsifying agents and/or dispersing agents and/or foam-forming agents.
  • organic solvents can, for example, also be used as auxiliary solvents.
  • liquid solvents there are suitable in the main: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulphoxide, as well as water.
  • aromatics such as xylene, toluene or alkylnaphthalenes
  • Adhesives such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latexes, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations. Further additives can be mineral and vegetable oils.
  • colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyes, such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • the formulations in general contain between 0.1 and 95 per cent by weight of active compound, preferably between 0.5 and 90%.
  • the active compounds according to the invention can also be used as mixtures with known herbicides, finished formulations or tank mixes being possible.
  • herbicides for example anilides, for example diflufenican and propanil; arylcarboxylic acids, for example dichloropicolinic acid, dicamba and picloram; aryloxyalkanoic acids, for example 2,4-D, 2,4-DB, 2,4-DP, fluroxypyr, MCPA, MCPP and triclopyr; aryloxy-phenoxy-alkanoic esters, for example diclofop-methyl, fenoxaprop-ethyl, fluazifop-butyl, haloxyfop-methyl and quizalofop-ethyl; azinones, for example chloridazon and norflurazon; carbamates, for example chlorpropham, desmedipham, phenmedipham and propham; chloroacetanilides, for example alachlor, acetochlor, butachlor, metazachlor, metolachlor, pretilachlor and propachlor
  • the active compounds can be used as such, in the form of their formulations or in the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in the customary manner, for example by watering, spraying, atomizing or scattering.
  • the active compounds according to the invention can be applied either before or after emergence of the plants. They can also be incorporated into the soil before sowing.
  • the amount of active compound used can vary within a substantial range. It depends essentially on the nature of the desired effect. In general, the amounts used are between 1 and 10 kg of active compound per hectare of soil surface, preferably between 5 g and 5 kg per ha.
  • DBU diazabicyclo [5.4.0]undec-7-ene
  • a mixture of 3.2 g (25 mmol) of 5-methyl-1,2,4-oxadiazole-3-carboxamide, 4.2 g (75 mmol) of potassium hydroxide (powder) and 200 ml of dioxane is stirred at 60° C. for 30 minutes. It is then concentrated to about half its volume under a water pump vacuum, and a solution of 7 g (30 mmol) of 2-ethoxy-6-methyl-benzenesulphochloride in 10 ml of dioxane is added dropwise at about 20° C. The reaction mixture is then stirred at 20° C. for about 15 hours more.
  • Example 9 The compound listed in Table 1 as Example 9 can be prepared, for example, as follows: (Process (b))
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
  • Seeds of the test plants are sown in normal soil, and, after 24 hours, the soil is watered with the preparation of the active compound. It is expedient to keep constant the amount of water per unit area.
  • the concentration of the active compound in the preparation is of no importance, only the amount of active compound applied per unit area being decisive.
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
  • Test plants which have a height of 5-15 cm are sprayed with the preparation of the active compound in such a way as to apply the particular amounts of active compound desired per unit area.
  • the concentration of the spray liquor is chosen so that the particular amounts of active compound desired are applied in 2,000 l of water/ha.
  • the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control.

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Abstract

The invention relates to novel sulphonylamino(thio) carbonyl compounds of the formula (I),
Figure USRE039607-20070501-C00001
in which
    • A represents a single bond, oxygen, sulphur or the group N—R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl,
    • Q represents oxygen or sulphur,
    • R1 represents hydrogen or formyl or represents in each case optionally substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkoxycarbonyl, alkylsulphonyl, cycloalkyl, cycloalkylcarbonyl or cycloalkylsulphonyl,
    • R2 represents cyano or halogen or represents in each case optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy or alkinyloxy, and
    • R3 represents in each case optionally substituted heterocyclyl having 5 ring members of which at least one is oxygen, sulphur or nitrogen and from one to three further ring members can be nitrogen,
      and salts of compounds of the formula (I),
    • the previously known compounds 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
    • and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl-1H-pyrazole-3-carboxamide being excluded by disclaimer;
    • and also to processes and novel intermediates for the preparation of the novel substances and to their use as herbicides.

Description

This is a Continuation of U.S. Ser. No. 09/006,686, filed on Jan. 8, 1998 (now abandoned); which is a Continuation-in-Part of International Application PCT/EP96/02826, filed on Jun. 28, 1996.
The invention relates to novel sulphonylamino(thio) carbonyl compounds, to a number of processes and to novel intermediates for their preparation, and to their use as herbicides.
It is already known that certain sulphonylaminocarbonyl compounds, such as, for example, the compounds 4,5-dimethoxy-2-(2-methoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl-1H-pyrazole-3-carboxamide possess herbicidal properties (cf. EP 341489, EP 422469, EP 425948, EP 431291, EP 507171, EP 534266, DE 4029753). The action of these compounds, however, is not in every respect satisfactory.
The novel sulphonylamino(thio)carbonyl compounds have now been found of the ageneral formula (I),
Figure USRE039607-20070501-C00002
in which
    • A represents a single bond, oxygen, sulphur or the group N—R, in which R represents hydrogen, alkyl, alkenyl, alkinyl or cycloalkyl,
    • Q represents oxygen or sulphur,
    • R1 represents hydrogen or formyl or represents in each case optionally substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkoxycarbonyl, alkylsulphonyl, cycloalkyl, cycloalkylcarbonyl or cycloalkylsulphonyl,
    • R2 represents cyano or halogen or represents in each case optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy or alkinyloxy, and
    • R3 represents in each case optionally substituted heterocyclyl having 5 ring members of which at least one is oxygen, sulphur or nitrogen and from one to three further ring members can be nitrogen,
      and salts of compounds of the formula (I),
    • the previously known compounds 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl-1H-pyrazole-3-carboxamide being excluded by disclaimer;
The novel sulphonylamino(thio)carbonyl compounds of the general formula (I) are obtained if
(a) aminosulphonyl compounds of the general formula (II)
Figure USRE039607-20070501-C00003
in which
    • A, R1 and R2 have the meanings given above
      are reacted with (thio)carboxylic acid derivatives of the general formula (III)
      Figure USRE039607-20070501-C00004
      in which
    • Q and R3 have the meanings given above and
    • Z represents halogen, alkoxy, aryloxy or arylalkoxy,
    • optionally in the presence of an acid acceptor and optionally in the presence of a diluent,
      or if
      (b) sulphonyl iso(thio)cyanates of the general formula (IV)
      Figure USRE039607-20070501-C00005
      in which
    • A, Q, R1 and R2 have the meanings given above
      are reacted with heterocycles of the general formula (V)
      H—R3  (V)
      in which
    • R3 has the meaning given above,
    • optionally in the presence of a reaction auxiliary and optionally in the presence of a diluent,
      or if
      (c) chlorosulphonyl compounds of the general formula (VI)
      Figure USRE039607-20070501-C00006
      in which
    • A, R1 and R2 have the meanings given above
      are reacted with heterocycles of the general formula (V)
      H—R3  (V)
      in which
    • R3 has the meaning given above
      and metal (thio)cyanates of the general formula (VII)
      MOCN  (VII)
      in which
    • Q has the meaning given above, and
    • M represents an alkali metal or alkaline earth metal equivalent,
    • optionally in the presence of a reaction auxiliary and optionally in the presence of a diluent,
      or if
      (d) chlorosulphonyl compounds of the general formula (VI)
      Figure USRE039607-20070501-C00007
      in which
    • A, R1 and R2 have the meanings given above
      are reacted with (thio)carboxamides of the general formula (VIII)
      Figure USRE039607-20070501-C00008
      in which
    • Q and R3 have the meanings given above,
    • optionally in the presence of an acid acceptor and optionally in the presence of a diluent,
      or if
      (e) sulphonylamino(thio)carbonyl compounds of the general formula (IX)
      Figure USRE039607-20070501-C00009
      in which
    • A, Q, R1 and R2 have the meanings given above, and
    • Z represents halogen, alkoxy, aryloxy or arylalkoxy,
      are reacted with heterocycles of the general formula (V)
      H—R3  (V)
      in which
    • R3 has the meaning given above,
    • optionally in the presence of an acid acceptor and optionally in the presence of a diluent,
      or if
      (f) heterocycles of the general formula (V)
      H—R3  (V)
      in which
    • R3 has the meaning given above,
      are reacted with chlorosulphonyl iso(thio)cyanate, optionally in the presence of a diluent, and the adducts formed in this reaction are reacted in situ with benzene derivatives of the general formula (X)
      Figure USRE039607-20070501-C00010
      in which
    • A, R1 and R2 have the meanings given above,
    • optionally in the presence of an acid acceptor and optionally in the presence of a diluent,
    • and, if desired, the compounds of the formula (I) obtained by processes (a), (b), (c), (d), (e) or (f) are converted into salts by customary methods.
The novel sulphonylamino(thio)carbonyl compounds of the general formula (I) are distinguished by a strong herbicidal activity.
The invention relates preferably to compounds of the formula (I) in which
    • A represents a single bond, oxygen, sulphur or the group N—R, in which R represents hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkinyl or C3-C6-cycloalkyl,
    • Q represents oxygen or sulphur,
    • R1 represents hydrogen or formyl or represents in each case optionally cyano-, fluoro-, chloro-, bromo-, phenyl- or C1-C4-alkoxy-substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkoxycarbonyl or alkylsulphonyl having in each case up to 6 carbon atoms, or represents in each case optionally cyano-, fluoro-, chloro-, bromo- or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C3-C6-cycloalkyl-carbonyl or C3-C6-cycloalkyl-sulphonyl,
    • R2 represents cyano, fluoro, chloro or bromo or represents in each case optionally cyano-, fluoro-, chloro-, bromo- or C1-C4-alkoxy-substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy or alkinyloxy having in each case up to 6 carbon atoms, and
    • R3 represents in each case optionally substituted heterocyclyl of the formulae below,
      Figure USRE039607-20070501-C00011
      in which
    • Q1, Q2 and Q3 each represent oxygen or sulphur, and
    • R4 represents hydrogen, hydroxyl, amino or cyano, or represents C2-C10-alkylideneamino, or represents optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy-, C1-C4-alkyl-carbonyl- or C1-C4-alkoxy-carbonyl-substituted C1-C6--alkyl, or represents in each case optionally fluoro-, chloro- and/or bromo-substituted C2-C6-alkenyl or C2-C6-alkinyl, or represents in each case optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkoxy, C1-C6-alkylamino or C1-C6-alkyl-carbonylamino, or represents C3-C6-alkenyloxy, or represents di-(C1-C6-alkyl)-amino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano- and/or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C3-C6-cycloalkylamino or C3-C6-cycloalkyl-C1-C4-alkyl, or represents in each case optionally fluoro-, chloro-, bromo-, cyano-, nitro-, C1-C4-alkyl-, trifluoromethyl- and/or C1-C4-alkoxy-substituted phenyl, phenylamino or phenyl-C1-C4-alkyl,
    • R5 represents hydrogen, hydroxyl, mercapto, amino, cyano, fluoro, chloro, bromo or iodo, or represents optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy-, C1-C4-alkyl-carbonyl- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkyl, or represents in each case optionally fluoro-, chloro- and/or bromo-substituted C2-C6-alkenyl or C2-C6-alkinyl, or represents in each case optionally fluoro-, chloro-, cyano-, C1-C4-alkoxy- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylamino or C1-C6-alkyl-carbonylamino, or represents C3-C6-alkenyloxy, C3-C6-alkinyloxy, C3-C6-alkenylthio, C3-C6-alkinylthio, C3-C6-alkenylamino or C3-C6-alkinylamino, or represents di-(C1-C4-alkyl)-amino, or represents in each case optionally methyl- and/or ethyl-substituted aziridino, pyrrolidino, piperidino or morpholino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano- and/or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C5-C6-cycloalkenyl, C3-C6-cycloalkyloxy, C3-C6-cycloalkylthio, C3-C6-cycloalkylamino, C3-C6-cycloalkyl-C1-C4-alkyl, C3-C6-cycloalkyl-C1-C4-alkoxy, C3-C6-cycloalkyl-C1-C4-alkylthio or C3-C6-cycloalkyl-C1-C-alkylamino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano-, nitro-, C1-C4-alkyl-, trifluoromethyl-, C1-C4-alkoxy- and/or C1-C4-alkoxy-carbonyl-substituted phenyl, phenyl-C1-C4-alkyl, phenoxy, phenyl-C1-C4-alkoxy, phenylthio, phenyl-C1-C4-alkylthio, phenylamino or phenyl-C1-C4-alkylamino, or
    • R4 and R5 together represent optionally branched alkanediyl having 3 to 11 carbon atoms, and also
    • R6, R7 and R8 are identical or different and represent hydrogen, cyano, fluoro, chloro or bromo, or represent in each case optionally fluoro-, chloro-, bromo- or C1-C4-alkoxy-substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy, alkylthio, alkenylthio, alkinylthio, alkylsulphinyl and alkylsulphonyl having in each case up to 6 carbon atoms, or represents in each case optionally cyano-, fluoro-, chloro-, bromo- or C1-C4-alkyl-substituted cycloalkyl having 3 to 6 carbon atoms,
    • the previously known compounds 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl-1H-pyrazole-3-carboxamide being excluded by disclaimer.
The invention also relates preferably to sodium, potassium, magnesium, calcium, ammonium, C1-C4-alkyl-ammonium, di-(C1-C4-alkyl)-ammonium, tri-(C1-C4-alkyl)-ammonium, tetra-(C1-C4-alkyl)-ammonium, tri-(C1-C4-alkyl)-sulphonium, C5- or C6-cycloalkyl-ammonium and di-(C1-C2-alkyl)-benzyl-ammonium salts
of compounds of the formula (I) in which A, Q, R1, R2 and R3 have the meanings indicated above as preferred.
The invention relates in particular to compounds of the formula (I) in which
    • A represents a single bond, oxygen or the group N—R, in which R represents hydrogen, methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, propenyl, butenyl, propinyl, butinyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
    • Q represents oxygen or sulphur,
    • R1 represents hydrogen or formyl, or represents in each case optionally fluoro-, chloro-, bromo-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, propenyl, butenyl, propinyl, butinyl, acetyl, propionyl, butyroyl, methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, n-, i-, s- or t-butylsulphonyl, or represents in each case optionally fluoro-, chloro- or methyl-substituted cyclopropyl, cyclopropylcarbonyl or cyclopropylsulphonyl,
    • R2 represents cyano, fluoro, chloro or bromo, or represents in each case optionally fluoro-, chloro-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, propenyl, butenyl, propinyl, butinyl, methoxy, ethoxy, n- or i-propoxy, n-, i- or s-butoxy, propenyloxy, butenyloxy, propinyloxy or butinyloxy and
    • R3 represents in each case optionally substituted heterocyclyl of the formulae below,
      Figure USRE039607-20070501-C00012
    •  in which
      • Q1, Q2 and Q3 each represent oxygen or sulphur, and
    • R4 represents hydrogen, hydroxyl or amino, or represents C3-C8-alkyli-deneamino, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, or represents in each case optionally fluoro-, chloro- or bromo-substituted propenyl, butenyl, propinyl or butinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, or represents propenyloxy or butenyloxy, or represents dimethylamino or diethylamino, or represents in each case optionally fluoro-, chloro-, methyl- and/or ethyl-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, or represents in each case optionally fluoro-, chloro-, methyl-, trifluoromethyl- and/or methoxy-substituted phenyl or benzyl,
    • R5 represents hydrogen, hydroxyl, mercapto, amino, fluoro, chloro or bromo, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, or represents in each case optionally fluoro-, chloro- or bromo-substituted ethenyl, propenyl, butenyl, propinyl or butinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, or represents propenyloxy, butenyloxy, propinyloxy, butinyloxy, propenylthio, propadienylthio, butenylthio, propinylthio, butinylthio, propenylamino, butenylamino, propinylamino or butinylamino, or represents dimethylamino, diethylamino or dipropylamino, or represents in each case optionally fluoro-, chloro-, methyl- and/or ethyl-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl, cyclohexenyl, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexymethoxy, cyclopropylmethylthio, cyclobutylmethylthio, cyclopentylmethylthio, cyclohexylmethylthio, cyclopropylmethylamino, cyclobutylmethylamino, cyclopentylmethylamino or cyclohexylmethylamino, or represents in each case optionally fluoro-, chloro-, methyl-, trifluoromethyl-, methoxy- and/or methoxy-carbonyl substituted phenyl, benzyl, phenoxy, benzyloxy, phenylthio, benzylthio, phenylamino or benzylamino, or
    • R4 and R5 together represent optionally branched alkanediyl having 3 to 11 carbon atoms, and also
    • R6, R7 and R8 are identical or different and represent hydrogen, cyano, fluoro, chloro or bromo, or represent in each case optionally fluoro-, chloro-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, propenyl, butenyl, propinyl, butinyl methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, propenyloxy, butenyloxy, propinyloxy, butinyloxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, propenylthio, butenylthio, propinylthio, butinylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl or ethylsulphonyl, or represent cyclopropyl,
    • the previously known compounds 4,5-dimethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, 4,5-diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one and N-(2,5-dimethoxy-phenylsulphonyl)-1,5-dimethyl1H-pyrazole-3-carboxamide being excluded by disclaimer.
A very particularly preferred group of compounds according to the invention are the compounds of the formula (I), in which
    • A represents a single bond,
    • Q represents oxygen or sulphur,
    • R1 represents methyl, ethyl, n- or i-propyl,
    • R2 represents chloro or methyl- in each case in position 5 or 6- and
    • R3 represents optionally substituted triazolinyl of the formula below,
      Figure USRE039607-20070501-C00013
    •  in which
      • Q1 represents oxygen or sulphur, and
      • R4 represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, or represents propenyl or propinyl, or represents methoxy, ethoxy, n- or i-propoxy, or represents cyclopropyl, and
      • R5 represents hydrogen, chloro or bromo, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, or represents in each case optionally fluoro and/or chloro-substituted propenyl or propinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, or represents propenyloxy or cyclopropyl.
The radical definitions listed above, whether general or listed in ranges of preference, apply not only to the end products of the formula (I) but also, correspondingly, to the starting materials and/or intermediates required in each case of the preparation. These radical definitions can be combined as desired with one another, thus including combinations between the preferred ranges indicated.
Using, for example, 2-fluoro-6-methoxy-benzenesulphonamide and 5-ethoxy-4-methyl-2-phenoxycarbonyl-2,4-dihydro-3H-1,2,4-triazol-3-thi one as starting materials, the course of reaction in the process (b) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00014
Using, for example, 2-ethoxy-6-methyl-phenylsulphonyl-isothiocyanate and 5-ethyl-4-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one as starting materials, the course of reaction in the process (b) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00015
Using, for example, 2-rnethoxy-3-methyl-benzenesulphochloride, 5-ethylthio-4-methoxy-2,4-dihydro-3H-1,2,4-triazol-3-one and potassium cyanate as starting materials, the course of reaction in the process (c) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00016
Using, for example, 2-ethoxy-4-fluoro-benzenesulphochloride and 5-methyl-1,2,4-oxadiazole-3-carboxamide as starting materials, the course of reaction in the process (d) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00017
Using, for example, N-(2-chloro-6-propoxy-phenylsulphonyl)-O-methyl-urethane and 4-methyl-5-methylthio-2,4-dihydro-3H-1,2,4-triazol-3-one as starting materials, the course of reaction in the process (e) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00018
Using, for example, 5-chloro-4-ethyl-2,4-dihydro-3H-1,2,4-triazol-3-one and chlorosulphonylisocyanate and then 2-ethoxy-6-methyl-aniline as starting materials, the course of reaction in the process (f) according to the invention can be illustrated by the following equation:
Figure USRE039607-20070501-C00019
A general definition of the aminosulphonyl compounds to be used as starting materials in the process (a) according to the invention for the preparation of compounds of the formula (I) is given by the formula (II). In the formula (II) A, R1 and R2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or, respectively, particularly preferable for A, R1 and R2.
The starting materials of the formula (II) are known and/or can be prepared by methods known per se (cf. EP 216504, DE 3208189, EP 44807, EP 23422).
Compounds not yet known from the literature, and which as novel substances are likewise a subject of the present application, are the sulphonamides of the general formula (IIa),
Figure USRE039607-20070501-C00020
in which
    • A1 represents ethyl, n- or i-propyl, n-, i-, s- or t-butyl, trifluoromethyl, fluoroethyl, chloroethyl, difluoroethyl, trifluoroethyl, chlorotrifluoroethyl, methoxyethyl, ethoxyethyl, allyl, propargyl or benzyl, and
    • A2 represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl.
The novel sulphonamides of the formula (IIa) are obtained if sulphonyl chlorides of the formula (VIa)
Figure USRE039607-20070501-C00021
in which
    • A1 and A2 have the meanings given above
    • are reacted with ammonia, optionally in the presence of a diluent, for example water, at temperatures between 0° C. and 50° C. (cf. the Preparation Examples).
The starting materials of the formula (II) can in general be obtained also by reacting phenol derivatives of the formula (IIb)
Figure USRE039607-20070501-C00022
in which
    • A and R2 have the meanings given above
      with alkylating agents of the formula (XI)
      X—R1  (XI)
      in which
    • R1 has the meaning given above, and
    • X represents halogen or the group R1—O—SO2—O—,
    • optionally in the presence of an acid acceptor, for example potassium carbonate, and optionally in the presence of a diluent, for example toluene, at temperatures between 10° C. and 150° C. (cf. the Preparation Examples).
The phenol derivatives of the formula (IIb) required as precursors are known and/or can be prepared by methods known per se (cf. EP 44807, Metalloberflache [Metal surface]—Angew. Elektrochemie 27 (1973), 217-227—cited in Chem. Abstracts 79:86733; Preparation Examples).
The alkylating agents of the formula (XI) which are also required as precursors are known synthesis chemicals.
A general definition of the (thio)carboxylic acid derivatives also to be used as starting materials in the process (a) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (III). In the formula (III), Q and R3 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or, respectively, particularly preferable for Q and R3; Z preferably represents fluorine, chlorine, bromine, C1-C4-alkoxy, phenoxy or benzyloxy, and in particular represents chlorine, methoxy, ethoxy or phenoxy.
The starting materials of the formula (III) are known and/or can be prepared by methods known per se (cf. EP 459244, EP 341489, EP 422469, EP 425948, EP 431291, EP 507171, EP 534266).
A general definition of the sulphonyl iso(thio)cyanate to be used as starting materials in the process (b) according to the invention for the preparation of the compounds of the formula (I) is given with the formula (IV). In the formula (IV), A, Q, R1 and R2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, Q, R1 and R2.
The starting materials of the formula (IV) are known and/or can be prepared by methods known per se (cf. EP 23422, EP 216504).
Compounds not yet known from the literature, and which as novel substances are likewise a subject of the present application, are the sulphonyl iso(thio)cyanates of the general formula (IVa)
Figure USRE039607-20070501-C00023
in which
    • Q represents oxygen or sulphur,
    • A1 represents ethyl, n- or i-propyl, n-, i-, s- or t-butyl, trifluoromethyl, fluoroethyl, chloroethyl, difluoroethyl, trifluoroethyl, chlorotrifluoroethyl, methoxyethyl, ethoxyethyl, allyl, propargyl or benzyl, and
    • A2 represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl.
The novel sulphonyl iso(thio)cyanates of the formula (IVa) are obtained if sulphonamides of the formula (IIa)—above—are reacted with phosgene or, respectively, thiophosgene, optionally in the presence of an alkyl isocyanate, for example butyl isocyanate, optionally in the presence of a reaction auxiliary, for example diazabicyclo [2.2.2]octane, and in the presence of a diluent, for example toluene, xylene or chlorobenzene, at temperatures between 80° C. and 150° C., and, after the end of the reaction, the volatile components are distilled off under reduced pressure.
A general definition of the heterocycles also to be used as starting materials in the processes (b), (c), (e) and (f) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (V). In the formula (V), R3 preferably or in particular has that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for R3.
The starting materials of the formula (V) are known and/or can be prepared by methods known per se (cf. EP 341489, EP 422469, EP 425948, EP 431291, EP 507171, EP 534266).
A general definition of the chlorosulphonyl compounds to be used as starting materials in the processes (c) and (d) according to the invention for the preparation of compounds of the formula (I) is given by the formula (VI). In the formula (VI), A, R1 and R2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, R1 and R2.
The starting materials of the formula (VI) are known and/or can be prepared by methods known per se (cf. EP 511826, DE 3208189, EP23422).
Compounds not yet known from the literature, which as novel substances are likewise a subject of the present application, are the sulphonyl chlorides of the formula (VIa)
Figure USRE039607-20070501-C00024
in which
    • A1 represents ethyl, n- or i-propyl, n-, i-, s- or t-butyl, trifluoromethyl, fluoroethyl, chloroethyl, difluoroethyl, trifluoroethyl, chlorotrifluoroethyl, methoxyethyl, ethoxyethyl, allyl, propargyl or benzyl, and
    • A2 represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl.
The novel sulphonyl chlorides of the formula (VIa) are obtained if aniline derivatives of the formula (XII)
Figure USRE039607-20070501-C00025
in which
    • A1 and A2 have the meanings given above
      dare reacted with an alkali metal nitrite, for example sodium nitrite, in the presence if hydrochloric acid at temperatures between −10° C. and +10° C., and the diazonium salt solution thus obtained is reacted with sulphur dioxide in the presence of a diluent, for example dichioromethane or 1,2-dichioro-ethane, and in the presence of a catalyst, for example copper(I) chloride, optionally in the presence of a further catalyst, for example dodecyltrimethylammonium bromide, at temperatures between −10° C. and +50° C. (cf. the Preparation Examples).
The aniline derivatives of the formula (XII) required as precursors are known and/or can be prepared by methods known per se (cf. EP 511826, US 4992091, EP 185128, DE 2405479, Preparation Examples).
The abovementioned novel benzenesulphonic acid derivatives of the formulae (IIa), (IVa) and (VIa) can be defined comprehensively by the following formula (XIII):
Figure USRE039607-20070501-C00026
in which
    • E represents —NH2, —N═C+Q or —Cl, where
    • Q represents O or S, and also
    • A1 represents ethyl, n- or i-propyl, n-, i-, s- or t-butyl, trifluoromethyl, fluoroethyl, chloroethyl, difluoroethyl, trifluoroethy, chlorotrifluoroethyl, methoxyethyl, ethoxyethyl, allyl, propargyl or benzyl, and
    • A2 represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl.
A general definition of the (thio)carboxamides to be used as starting materials in the process (d) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (VIII). In the formula (VIII), Q and R3 preferably or in particular have that meaning which has already been indicated above, in connection with a description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for Q and R3.
The starting materials of the formula (VIII) are known and/or can be prepared by methods known per se (cf. EP 459244).
A general definition of the sulphonylamino(thio)carbonyl compounds to be used as starting materials in the process (e) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (IX). In the formula (IX), A, Q, R1 and R2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, Q, R1 and R2; Z preferably represents fluoro, chloro, bromo, C1-C4-alkoxy, phenoxy or benzyloxy, and in particular represents chlorine, methoxy, ethoxy or phenoxy.
A general definition of the benzene derivatives to be used as starting materials in the process (f) according to the invention for the preparation of the compounds of the formula (I) is given by the formula (X). In the formula (X), A, R1 and R2 preferably or in particular have that meaning which has already been indicated above, in connection with the description of the compounds of the formula (I) to be prepared in accordance with the invention, as being preferable or particularly preferable for A, R1 and R2.
Starting materials of the formula (X) are known and/or can be prepared by methods known per se (cf. EP 511826, U.S. Pat. No. 4,992,091, EP 185128, DE 2405479, Preparation Examples).
The processes (a), (b), (c), (d), (e) and (f) according to the invention for the preparation of the novel compounds of the formula (I) are preferably carried out using diluents. Suitable diluents in this context are virtually all inert organic solvents. These include, preferably, aliphatic and aromatic, optionally halogenated hydrocarbons such as pentane, hexane, heptane, cyclohexane, petroleum ether, benzine, ligroin, benzene, toluene, xylene, methylene chloride, ethylene chloride, chloroform, tetrachloromethane, chlorobenzene and o-dichlorobenzene; ethers such as diethyl ether and dibutyl ether, glycol dimethyl ether and diglycol dimethyl ether, tetrahydrofuran and dioxanes; ketones such as acetone, methyl ethyl ketone, methyl isopropyl ketone and methyl isobutyl ketone; esters such as methyl acetate and ethyl acetate; nitrites, for example acetonitrile and propionitrile; amides, for example dimethylformamide, dimethylacetamide and N-methylpyrrolidone, and also dimethyl sulphoxide, tetramethylene sulphone and hexamethylphosphoric triamide.
As reaction auxiliaries and/or as acid acceptors in the processes (a), (b), (c), (d), (e) and (f) according to the invention it is possible to employ all acid-binding agents which can customarily be used for such reactions. Preferred among suitable examples are alkali metal hydroxides, for example sodium, hydroxide and potassium hydroxide, alkaline earth metal hydroxides, for example calcium hydroxide, alkali metal carbonates and alcoholates, such as sodium carbonate and potassium carbonate, sodium tert-butylate and potassium tert-butylate, and also basic nitrogen compounds such as trimethylamine, triethylamine, tripropylamine, tributylamine, diisobutylamine, dicyclohexylamine, ethyldiisopropylamine, ethyldicyclohexylamine, N,N-dimethylbenzylamine, N,N-dimethyl-aniline, pyridine, 2-methyl-, 3-methyl-, 4-methyl-, 2,4-dimethyl-, 2,6-dimethyl-, 2-ethyl-, 4-ethyl- and 5-ethyl-2-methyl-pyridine, 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN), 1,8-diazabicyclo [5.4.0]-undec-7-ene (DBU) and 1,4-diazabicyclo-[2.2.2]-octane (DABCO).
The reaction temperatures in the processes (a), (b), (c), (d), (e) and (f) according to the invention can be varied within a relatively wide range. They are in general carried out at temperatures of between −20° C. and +150° C., preferably at temperatures between 0° C. and +100° C.
The processes (a), (b), (c), (d), (e) and (f) according to the invention are generally carried out under atmospheric pressure. However it is also possible to operate under increased or reduced pressure.
For carrying out processes (a), (b), (c), (d), (e) and (f) according to the invention, the starting materials required in each case are in general employed in approximately equimolar quantities. However, it is also possible to use one of the components employed in each case in a relatively large excess. The reactions are in general carried out in a suitable diluent in the presence of an acid acceptor, and the reaction mixture is stirred for a number of hours at the particular temperature required. Working up in the case of the processes (a), (b), (c), (d), (e) and (f) according to the invention is in each case by customary methods (cf. the Preparation Examples).
Salts of the compounds of the general formula (I) according to the invention can be prepared if desired. Such salts are obtained in a simple manner by customary methods of forming salts, for example by dissolving or dispersing a compound of the formula (I) in an appropriate solvent, for example methylene chloride, acetone, tert-butyl methyl ether or toluene, and adding an appropriate base. The salts can then—if desired after prolonged stirring—be isolated by concentration or filtration with suction.
The active compounds according to the invention can be used as defoliants, desiccants, agents for destroying broad-leaved plants and, especially, as weed-killers. By weeds, in the broadest sense, there are to be understood all plants which grow in locations where they are not wanted. Whether the substances according to the invention act as total or selective herbicides depends essentially on the amount used.
The active compounds according to the invention can be used, for example, in connection with the following plants:
Dicotyledon weeds of the genera: Sinapis, Lepidium, Galium, Stellaria, Matricaria, Anthemis, Galinsoga, Chenopodium, Urtica, Senecio, Amaranthus, Portulaca, Xanthium, Convolvulus, Ipomoea, Polygonum, Sesbania, Ambrosis, Cirsium, Carduus, Sonchus, Solanum, Rorippa, Rotala, Lindernia, Lamium, Veronica, Abutilon, Emex, Datura, Viola, Galeopsis, Papaver Centaurea, Trifolium, Ranunculus and Taraxacum.
Dicotyledon cultures of the genera: Gossypium, Glycine, Beta, Daucus, Phaseolus, Pisum, Solanum, Linum, Ipomoea, Vicia, Nicotians, Lycopersicon, Arachis, Brassica, Lactuca, Cucumis and Cucurbita.
Monocotyledon weeds of the genera: Echinochloa, Setaria, Panicum, Digitaria, Phleum, Poa, Festuca, Eleusine, Brachiaria, Lolium, Bromus, Avena, Cyperus, Sorghum, Agropyron, Cynodon, Monochoria, Fimbristylis, Sagittaria, Eleocharis, Scirpus, Paspalum, Ischaemum, Sphenoclea, Dactyloctenium, Agrostis, Alopecurus and Apera.
Monocotyledon cultures of the genera: Oryza, Zea, Triticum, Hordeum, Avena, Secale, Sorghum, Panicum, Saccharum, Ananas, Asparagus and Allium.
However, the use of the active compounds according to the invention is in no way restricted to these genera, but also extends in the same manner to other plants.
The compounds are suitable, depending on the concentration, for the total combating of weeds, for example on industrial terrain and rail tracks, and on paths and squares with or without tree plantings. Equally, the compounds can be employed for combating weeds in perennial cultures, for example afforestations, decorative tree plantings, orchards, vineyards, citrus groves, nut orchards, banana plantations, coffee plantations, tea plantations, rubber plantations, oil palm plantations, cocoa plantations, soft fruit plantings and hopfields, in lawns, turf and pasture-land, and for the selective combating of weeds in annual cultures.
The compounds of the formula (I) according to the invention are preferably suitable for combating monoctyledon and dicotyledon broad-leaved weeds, both pre-emergence and post-emergence. They exhibit strong herbicidal activity and a broad spectrum action when used on the soil and on above-ground parts of the plants.
The active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusting agents, pastes, soluble powders, granules, suspension-emulsion concentrates, natural and synthetic materials impregnated with active compound, and very fine capsules in polymeric substances.
These formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surface-active agents, that is emulsifying agents and/or dispersing agents and/or foam-forming agents.
In the case of the use of water as an extender, organic solvents can, for example, also be used as auxiliary solvents. As liquid solvents, there are suitable in the main: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulphoxide, as well as water.
As solid carriers there are suitable:
    • for example ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as highly disperse silica, alumina and silicates, as solid carriers for granules there are suitable: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, as well as synthetic granules of inorganic and organic meals, and granules of organic material such as sawdust, coconut shells, maize cobs and tobacco stalks; as emulsifying and/or foam forming agents there are suitable: for example non-ionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates as well as albumen hydrolysis products; as dispersing agents there are suitable: for example lignin-sulphite waste liquors and methylcellulose.
Adhesives such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latexes, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations. Further additives can be mineral and vegetable oils.
It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyes, such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
The formulations in general contain between 0.1 and 95 per cent by weight of active compound, preferably between 0.5 and 90%.
For controlling weeds, the active compounds according to the invention, as such or in the form of their formulations, can also be used as mixtures with known herbicides, finished formulations or tank mixes being possible.
Possible components for the mixtures are known herbicides, for example anilides, for example diflufenican and propanil; arylcarboxylic acids, for example dichloropicolinic acid, dicamba and picloram; aryloxyalkanoic acids, for example 2,4-D, 2,4-DB, 2,4-DP, fluroxypyr, MCPA, MCPP and triclopyr; aryloxy-phenoxy-alkanoic esters, for example diclofop-methyl, fenoxaprop-ethyl, fluazifop-butyl, haloxyfop-methyl and quizalofop-ethyl; azinones, for example chloridazon and norflurazon; carbamates, for example chlorpropham, desmedipham, phenmedipham and propham; chloroacetanilides, for example alachlor, acetochlor, butachlor, metazachlor, metolachlor, pretilachlor and propachlor; dinitroanilines, for example oryzalin, pendimethalin and trifluralin; diphenyl ethers, for example acifluorfen, bifenox, fluoroglycofen, fomesafen, halosafen, lactofen and oxyfluorfen; ureas, for example chlorotoluron, diuron, fluometuron, isoproturon, linuron and methabenzthiazuron; hydroxylamines, for example alloxydim; clethodim, cycloxydim, sethoxydim and tralkoxydim; imidazolinones, for example imazethapyr, imazamethabenz, imazapyr and imazaquin; nitriles, for example bromoxynil, dichlobenil and ioxynil; oxyacetamides, for example mefenacet; sulphonyl-ureas, for example amidosulfuron, bensulfuron-methyl, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, metsulfuron-methyl, nicosulfuron, primisulfuron, pyrazosulfuron-ethyl, thifensulfuron-methyl, triasulfuron and tribenuron-methyl; thiocarbamates, for example, butylate, cycloate, diallate, EPTC, esprocarb, molinate, prosulfocarb, thiobencarb and triallate; triazines, for example atrazine, cyanazine, simazine, simetryne, terbutryne and terbutylazine; triazinones, for example hexazinone, metamitron and metribuzin; others, for example aminotriazole, benfuresate, bentazone, cinmethylin, clomazone, clopyralid, difenzoquat, dithiopyr, ethofumesate, fluorochloridone, glufosinate, glyphosate, isoxaben, pyridate, quinchlorac, quimerac, sulphosate and tridiphane.
Mixtures with other known active compounds, such as fungicides, insecticides, acaricides, nematicides, bird repellants, plant nutrients and agents which improve soil structure, are also possible.
The active compounds can be used as such, in the form of their formulations or in the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in the customary manner, for example by watering, spraying, atomizing or scattering.
The active compounds according to the invention can be applied either before or after emergence of the plants. They can also be incorporated into the soil before sowing.
The amount of active compound used can vary within a substantial range. It depends essentially on the nature of the desired effect. In general, the amounts used are between 1 and 10 kg of active compound per hectare of soil surface, preferably between 5 g and 5 kg per ha.
The preparation and use of the active compounds according to the invention can be seen from the following examples.
PREPARATION EXAMPLES
Figure USRE039607-20070501-C00027
 (Process (a))
A mixture of 2.5 g (10 mmol) of 5-ethoxy-4-methyl-2-phenoxycarbonyl-2,4-dihydro-3H-1,2,4-triazol-3-one, 2.3 g (10 mmol) of 2-isopropoxy-6-methyl-benzenesulphonamide, 1.5 g (10 mmol) of diazabicyclo [5.4.0]undec-7-ene (DBU) and 50 ml of acetonitrile is stirred at 20° C. for 5 hours. It is then concentrated under a water pump vacuum and the residue is stirred with 50 ml of 1N hydrochloric acid, the mixture is filtered with suction, the filter product is stirred with diethyl ether and the mixture is again filtered with suction.
2.4 g (60% of theory) of 5-ethoxy-4-methyl-2-(2-isopropoxy-6-methyl-phenylsulphonyl-aminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained of melting point 155° C.
Figure USRE039607-20070501-C00028
(Process (c))
A mixture of 1.7 g (10 mmol) of 4-methyl-5-propargylthio-2,4-dihydro-3H-1,2,4-triazol-3-one, 1.3 g (20 mmol) of sodium cyanate, 2.5 g (10 mmol) of 2-methyl-6-n-propoxy-benzenesulphochloride and 50 ml of acetonitrile is heated under reflux for 3 hours. It is then concentrated under a water pump vacuum, the residue is stirred with 1N hydrochloric acid and the mixture is subjected three times to extraction with 50 ml of methylene chloride each time. The combined organic extraction solutions are concentrated, the residue is digested with isopropanol and the crystalline product is isolated by filtration with suction.
2.2 g (52% of theory) of 4-methyl-5-propargylthio-2-(2-methyl-6-n-propoxy-phenylsulphonyl-aminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained of melting point 151° C.
Figure USRE039607-20070501-C00029
(Process (d))
A mixture of 3.2 g (25 mmol) of 5-methyl-1,2,4-oxadiazole-3-carboxamide, 4.2 g (75 mmol) of potassium hydroxide (powder) and 200 ml of dioxane is stirred at 60° C. for 30 minutes. It is then concentrated to about half its volume under a water pump vacuum, and a solution of 7 g (30 mmol) of 2-ethoxy-6-methyl-benzenesulphochloride in 10 ml of dioxane is added dropwise at about 20° C. The reaction mixture is then stirred at 20° C. for about 15 hours more. It is then concentrated under a water pump vacuum, the residue is stirred with 50 ml of 1N hydrochloric acid and the crystalline product is isolated by filtration with suction. 4.0 g (49% of theory) of N-(2-ethoxy-6-methyl-phenylsulphonyl)-5-methyl-1,2,4-oxadiazole-3-carboxamide are obtained of melting point 168° C.
Figure USRE039607-20070501-C00030
(Process (f))
1.7 g (12 mmol) of chlorosulphonyl isocyanate are added to a solution, cooled to 5° C., of 1.4 g (10 mmol) of 5-ethoxy-4-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one in 50 ml of methylene chloride, and then a solution of 1.5 g (10 mmol) of 2-ethoxy-6-methyl-aniline and 1.0 g (10 mmol) of triethylamine in 10 ml of methylene chloride is added dropwise, likewise at 5° C. The reaction mixture is then stirred at about 20° C. For 15 hours. Subsequently, 100 ml of 1N hydrochloric acid are added. After a thorough stirring, the organic phase is separated off, dried over sodium sulphate and filtered. The filtrate is concentrated under water pump vacuum, the residue is digested with isopropanol and the crystalline product is isolated by filtration with suction.
1.8 g (45% of theory) of 5-ethoxy-4-methyl-2-(2-ethoxy-6-methyl-phenyl-aminosulphonyl-aminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained of melting point 147° C.
In analogy to Example 1 to 4 and in accordance with the general description of the preparation processes according to the invention, it is also possible, for example, to prepare the compounds of the formula (I) listed in Table 1 below (showing Examples Nos. 5-965), as well as the compounds of the formula (IA) listed in Table IA thereafter (showing Examples Nos. 966-1637):
TABLE 1
Examples of the compounds of the formula (I)
(I)
Figure USRE039607-20070501-C00031
Melting
Ex. (position-) point
No. A Q R1 R2 R3 (° C.)
 5 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00032
 		117
 6 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00033
 		156
 7 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00034
 		110
 8 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00035
 		141
 9 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00036
 		162
 10 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00037
 		126
 11 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00038
 		150
 12 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00039
 		129
 13 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00040
 		153
 14 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00041
 		167
 15 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00042
 		167
 16 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00043
 		125
 17 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00044
 		131
 18 — O C2H5 (5-)CH3
Figure USRE039607-20070501-C00045
 		222
 19 — O C2H5 (5-)CH3
Figure USRE039607-20070501-C00046
 		139
 20 — O C2H5 (4-)CH3
Figure USRE039607-20070501-C00047
 		189
 21 — O C2H5 (5-)CH3
Figure USRE039607-20070501-C00048
 		131
 22 — O —C2H4OC2H5 (6-)CH3
Figure USRE039607-20070501-C00049
 		118
 23 — O —CH2CH2Cl (6-)CH3
Figure USRE039607-20070501-C00050
 		137
 24 — O —CH2CH2Cl (6-)CH3
Figure USRE039607-20070501-C00051
 		149
 25 — O i-C3H7 (5-)CH3
Figure USRE039607-20070501-C00052
 		125
 26 — O i-C3H7 (5-)CH3
Figure USRE039607-20070501-C00053
 		140
 27 — O n-C3H7 (5-)CH3
Figure USRE039607-20070501-C00054
 		119
 28 — O n-C3H7 (5-)CH3
Figure USRE039607-20070501-C00055
 		134
 29 — O n-C3H7 (5-)CH3
Figure USRE039607-20070501-C00056
 		110
 30 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00057
 		108
 31 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00058
 		173
 32 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00059
 		119
 33 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00060
 		121
 34 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00061
 		109
 35 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00062
 		111
 36 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00063
 		 91
 37 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00064
 		130
 38 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00065
 		126
 39 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00066
 		101
 40 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00067
 		152
 41 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00068
 		100
 42 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00069
 		120
 43 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00070
 		117
 44 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00071
 		126
 45 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00072
 		113
 46 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00073
 		130
 47 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00074
 		139
 48 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00075
 		121
 49 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00076
 		119
 50 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00077
 		128
 51 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00078
 		134
 52 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00079
 		130
 53 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00080
 		117
 54 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00081
 		134
 55 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00082
 		141
 56 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00083
 		132
 57 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00084
 		166
 58 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00085
 		118
 59 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00086
 		150
 60 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00087
 		144
 61 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00088
 		170
 62 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00089
 		120
 63 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00090
 		124
 64 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00091
 		125
 65 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00092
 		116
 66 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00093
 		152
 67 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00094
 		143
 68 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00095
 		160
 69 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00096
 		133
 70 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00097
 		 97
 71 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00098
 		 96
 72 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00099
 		156
 73 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00100
 		145
 74 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00101
 		120
 75 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00102
 		125
 76 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00103
 		140
 77 — O H (6-)CH3
Figure USRE039607-20070501-C00104
 		 88
 78 — O C2H5 (5-)CH3
Figure USRE039607-20070501-C00105
 		130
 79 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00106
 		141
 80 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00107
 		 98
 81 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00108
 		141
 82 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00109
 		101
 83 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00110
 		136
 84 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00111
 		 96
 85 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00112
 		 90
 86 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00113
 		136
 87 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00114
 		122
 88 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00115
 		154
 89 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00116
 		139
 90 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00117
 		142
 91 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00118
 		153
 92 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00119
 		145
 93 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00120
 		132
 94 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00121
 		141
 95 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00122
 		130
 96 — O CH3 (5-)CH3
Figure USRE039607-20070501-C00123
 		156
 97 — O CH3 (5-)CH3
Figure USRE039607-20070501-C00124
 		177
 98 — O CH3 (4-)CH3
Figure USRE039607-20070501-C00125
 		115
 99 — O CH3 (4-)CH3
Figure USRE039607-20070501-C00126
 		166
100 — O CH3 (3-)CH3
Figure USRE039607-20070501-C00127
 		162
101 — O CH3 (3-)CH3
Figure USRE039607-20070501-C00128
 		143
102 — O CH3 (3-)CH3
Figure USRE039607-20070501-C00129
 		165
103 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00130
 		176
104 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00131
 		119
105 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00132
 		126
106 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00133
 		151
107 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00134
 		188
108 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00135
 		137
109 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00136
 		117
110 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00137
 		155
111 — O CHF2 (4-)CH3
Figure USRE039607-20070501-C00138
 		152
112 — O CHF2 (4-)CH3
Figure USRE039607-20070501-C00139
 		176
113 — O CHF2 (4-)CH3
Figure USRE039607-20070501-C00140
 		108
114 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00141
 		163
115 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00142
 		136
116 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00143
 		118
117 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00144
 		104
118 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00145
 		 98
119 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00146
 		128
120 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00147
 		165
121 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00148
 		155
122 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00149
 		105
123 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00150
 		 81
124 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00151
 		174
125 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00152
 		150
126 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00153
 		124
127 — O CHF2 (6-)CH3
Figure USRE039607-20070501-C00154
 		200
128 — S n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00155
 		160
129 — S n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00156
 		148
130 — S C2H5 (6-)CH3
Figure USRE039607-20070501-C00157
 		141
131 — S C2H5 (6-)CH3
Figure USRE039607-20070501-C00158
 		125
132 — S C2H5 (6-)CH3
Figure USRE039607-20070501-C00159
 		158
133 — S i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00160
 		155
134 — S n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00161
 		153
135 — S n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00162
 		131
136 — S n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00163
 		120
137 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00164
 		149
138 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00165
 		 99
139 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00166
 		176
140 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00167
 		192
141 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00168
 		144
142 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00169
 		114
143 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00170
 		144
144 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00171
 		157
145 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00172
 		142
146 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00173
 		191
147 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00174
 		116
148 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00175
 		205
149 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00176
 		147
150 — O C2H5 (6-)Cl
Figure USRE039607-20070501-C00177
 		117
151 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00178
 		149
152 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00179
 		176
153 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00180
 		150
154 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00181
 		146
155 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00182
 		191
156 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00183
 		127
157 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00184
 		174
158 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00185
 		117
159 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00186
 		134
160 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00187
 		115
161 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00188
 		137
162 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00189
 		125
163 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00190
 		119
164 — O H (6-)Cl
Figure USRE039607-20070501-C00191
 		147
165 — O n-C3H7 (6-)Cl
Figure USRE039607-20070501-C00192
 		148
166 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00193
 		143
167 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00194
 		122
168 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00195
 		165
169 — O n-C3H7 (5-)Cl
Figure USRE039607-20070501-C00196
 		154
170 — O n-C3H7 (5-)Cl
Figure USRE039607-20070501-C00197
 		136
171 — O n-C3H7 (5-)Cl
Figure USRE039607-20070501-C00198
 		128
172 — O CH3 (6-)Cl
Figure USRE039607-20070501-C00199
 		143
173 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00200
 		136
174 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00201
 		121
175 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00202
 		158
176 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00203
 		141
177 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00204
 		127
178 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00205
 		143
179 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00206
 		129
180 — O i-C3H7 (6-)Cl
Figure USRE039607-20070501-C00207
 		 95
181 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00208
 		 74
182 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00209
 		114
183 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00210
 		140
184 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00211
 		159
185 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00212
 		107
186 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00213
 		132
187 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00214
 		132
188 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00215
 		110
189 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00216
 		159
190 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00217
 		138
191 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00218
 		147
192 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00219
 		114
193 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00220
 		125
194 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00221
 		126
195 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00222
 		151
196 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00223
 		121
197 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00224
 		147
198 NH O C2H5 (6-)CH3
Figure USRE039607-20070501-C00225
 		135
199 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00226
 		263 (Sodium salt)
200 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00227
 		119
201 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00228
 		146
202 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00229
 		128
203 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00230
 		186
204 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00231
 		239
205 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00232
 		152
206 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00233
 		155
207 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00234
 		145 (Na salt)
208 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00235
 		209 (Na salt)
209 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00236
 		147 (Na salt)
210 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00237
 		140
211 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00238
 		118
212 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00239
 		156
213 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00240
 		110
214 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00241
 		133
215 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00242
 		138
216 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00243
 		154
217 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00244
 		149
218 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00245
 		112
219 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00246
 		162
220 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00247
 		 99
221 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00248
 		146
222 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00249
 		134
223 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00250
 		199
224 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00251
 		176
225 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00252
 		145
226 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00253
 		133
227 NH O n-C3H7 (5-)CH3
Figure USRE039607-20070501-C00254
 		127
228 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00255
 		144
229 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00256
 		141
230 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00257
 		152
231 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00258
 		132
232 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00259
 		147
233 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00260
 		163
234 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00261
 		102
235 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00262
 		121
236 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00263
 		113
237 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00264
 		145
238 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00265
 		137
239 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00266
 		172
240 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00267
 		148
241 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00268
 		157
242 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00269
 		186
243 NH O CH3 (6-)OCH3
Figure USRE039607-20070501-C00270
 		170
244 — O CHF2 (5-)CH3
Figure USRE039607-20070501-C00271
245 — S i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00272
 		160
246 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00273
 		205
247 — S CH3 (6-)CF3
Figure USRE039607-20070501-C00274
 		 92
248 — S CH3 (6-)CF3
Figure USRE039607-20070501-C00275
 		154
249 — S CH3 (6-)CF3
Figure USRE039607-20070501-C00276
 		157
250 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00277
 		176
251 — O n-C3H7-n (6-)CF3
Figure USRE039607-20070501-C00278
 		166
252 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00279
 		190
253 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00280
 		203
254 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00281
 		156
255 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00282
 		170
256 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00283
 		198
257 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00284
 		213
258 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00285
 		152
259 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00286
 		187
260 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00287
 		210
261 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00288
 		172
262 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00289
 		145
263 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00290
 		136
264 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00291
 		153
265 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00292
 		136
266 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00293
 		210
267 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00294
 		147
268 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00295
 		169
269 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00296
 		215
270 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00297
 		138
271 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00298
 		182
272 — S C2H5 (6-)CF3
Figure USRE039607-20070501-C00299
 		112
273 — S C2H5 (6-)CF3
Figure USRE039607-20070501-C00300
 		167
274 — S C2H5 (6-)CF3
Figure USRE039607-20070501-C00301
 		152
275 — S n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00302
 		119
276 — S n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00303
 		157
277 — S n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00304
 		154
278 — S i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00305
 		137
279 — S i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00306
 		167
280 — S i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00307
 		137
281 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00308
 		154
282 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00309
 		160
283 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00310
 		139
284 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00311
 		134
285 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00312
 		142
286 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00313
 		120
287 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00314
 		130
288 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00315
 		127
289 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00316
 		116
290 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00317
 		126
291 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00318
 		113
292 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00319
 		151
293 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00320
 		157
294 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00321
 		171
295 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00322
 		137
296 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00323
 		125
297 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00324
 		109
298 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00325
 		138
299 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00326
 		130
300 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00327
 		165
301 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00328
 		148
302 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00329
 		147
303 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00330
 		172
304 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00331
 		147
305 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00332
 		136
306 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00333
 		124
307 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00334
 		 98
308 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00335
 		125
309 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00336
 		179
310 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00337
 		153
311 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00338
 		171
312 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00339
 		113
313 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00340
 		138
314 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00341
 		110
315 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00342
 		134
316 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00343
 		167
317 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00344
 		120
318 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00345
 		117
319 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00346
 		160
320 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00347
 		154
321 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00348
 		159
322 — O n-C3H7 (6-)CF3
Figure USRE039607-20070501-C00349
 		141
323 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00350
 		146
324 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00351
 		134
325 — O i-C3H7 (6-)CF3
Figure USRE039607-20070501-C00352
 		168
326 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00353
 		158
327 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00354
 		172
328 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00355
 		147
329 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00356
 		 66
330 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00357
 		134
331 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00358
 		149
332 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00359
 		114
333 — O H (6-)Cl
Figure USRE039607-20070501-C00360
 		102
334 — O H (6-)Cl
Figure USRE039607-20070501-C00361
 		143
335 — O
Figure USRE039607-20070501-C00362
 		(6-)Cl
Figure USRE039607-20070501-C00363
 		130
336 — O —CH2C6H5 (6-)Cl
Figure USRE039607-20070501-C00364
 		143
337 — O —CH2C6H5 (6-)Cl
Figure USRE039607-20070501-C00365
 		 99
338 — O —CH2O≡CH (6-)Cl
Figure USRE039607-20070501-C00366
 		161
339 — O n-C3H7 (6-)CH3
Figure USRE039607-20070501-C00367
 		133
340 — O H (6-)CH3
Figure USRE039607-20070501-C00368
 		100
341 — O H (6-)CH3
Figure USRE039607-20070501-C00369
 		147
342 — O —CH2C6H5 (6-)CH3
Figure USRE039607-20070501-C00370
 		157
343 — O
Figure USRE039607-20070501-C00371
 		(6-)CH3
Figure USRE039607-20070501-C00372
 		150
344 — O —CH2C≡CH (6-)CH3
Figure USRE039607-20070501-C00373
 		172
345 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00374
 		263 (Na salt)
346 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00375
 		136
347 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00376
 		113
348 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00377
 		175
349 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00378
 		135
350 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00379
 		 78
351 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00380
 		125
352 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00381
 		140
353 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00382
 		161
354 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00383
 		142
355 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00384
 		124
356 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00385
 		153
357 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00386
 		170
358 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00387
 		116
359 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00388
 		120
360 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00389
 		172
361 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00390
 		175
362 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00391
 		192
363 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00392
 		195
364 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00393
 		174
365 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00394
 		160
366 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00395
 		214
367 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00396
 		185
368 — O CH3 (5-)Cl
Figure USRE039607-20070501-C00397
 		191
369 NH O CH3 (6-)CH3
Figure USRE039607-20070501-C00398
 		161
370 NH O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00399
 		132
371 NH O CH3 (6-)OCH3
Figure USRE039607-20070501-C00400
 		151
372 NH O CH3 (6-)CH3
Figure USRE039607-20070501-C00401
 		161
373 NH O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00402
 		128
374 NH O CH3 (6-)CH3
Figure USRE039607-20070501-C00403
 		140
375 — S i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00404
 		108
376 — O CHF2 (4-)CH3
Figure USRE039607-20070501-C00405
 		131
377 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00406
 		187
378 — O CH3 (6-)CF3
Figure USRE039607-20070501-C00407
 		154
379 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00408
 		179
380 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00409
 		178
381 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00410
 		167
382 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00411
 		135
383 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00412
 		146
384 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00413
 		174
385 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00414
 		130
386 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00415
 		195
387 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00416
 		183
388 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00417
 		135
389 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00418
 		149
390 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00419
 		193
391 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00420
 		125
392 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00421
 		182
393 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00422
 		120
394 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00423
 		158
395 — O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00424
 		180
396 — O n-C4H9 (6-)CH3
Figure USRE039607-20070501-C00425
 		132
397 — O n-C4H9 (6-)CH3
Figure USRE039607-20070501-C00426
 		143
398 — O n-C4H9 (6-)CH3
Figure USRE039607-20070501-C00427
 		106
399 — O n-C4H9 (6-)CH3
Figure USRE039607-20070501-C00428
 		 98
400 — O n-C4H9 (6-)CH3
Figure USRE039607-20070501-C00429
 		140
401 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00430
 		147
402 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00431
 		123
403 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00432
 		185
404 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00433
 		154
405 NH O i-C3H7 (6-)CH3
Figure USRE039607-20070501-C00434
 		150
406 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00435
 		135
407 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00436
 		134
408 — O C2H5 (6-)C2H5
Figure USRE039607-20070501-C00437
 		178
409 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00438
 		109
410 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00439
 		125
411 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00440
 		161
412 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00441
 		114
413 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00442
 		142
414 — O C3H7-i (6-)C2H5
Figure USRE039607-20070501-C00443
 		124
415 — O CH3 (6-)C2H5
Figure USRE039607-20070501-C00444
 		175 (Na salt)
416 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00445
 		126
417 — O C2H5 (6-)C3H7-n
Figure USRE039607-20070501-C00446
 		121
418 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00447
 		109
419 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00448
 		145
420 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00449
 		126
421 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00450
 		130
422 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00451
 		155
423 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00452
 		133
424 — O CH3 (6-)C3H7-n
Figure USRE039607-20070501-C00453
 		145
425 — O —SO2CH3 (6-)CH3
Figure USRE039607-20070501-C00454
 		 95
426 — O —SO2CH3 (6-)CH3
Figure USRE039607-20070501-C00455
 		153
427 — O C4H9-n (6-)CH3
Figure USRE039607-20070501-C00456
 		154
428 — O —CH2C≡CH (6-)CH3
Figure USRE039607-20070501-C00457
 		167
429 — O —CH2C≡CH (6-)CH3
Figure USRE039607-20070501-C00458
 		170
430 — O —CH2C≡CH (6-)CH3
Figure USRE039607-20070501-C00459
 		153
431 — O C4H9-i (6-)CH3
Figure USRE039607-20070501-C00460
 		123
432 — O C4H9-i (6-)CH3
Figure USRE039607-20070501-C00461
 		145
433 — O C4H9-i (6-)CH3
Figure USRE039607-20070501-C00462
 		143
434 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00463
 		138
435 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00464
 		161
436 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00465
 		128
437 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00466
 		177
438 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00467
 		165
439 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00468
 		157
440 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00469
 		168
441 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00470
 		164
442 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00471
 		125
443 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00472
 		162
444 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00473
 		154
445 — S CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00474
 		116
446 — S CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00475
 		110
447 — S CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00476
 		134
448 — O CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00477
 		152
449 — O CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00478
 		159
450 — O CH3 (4-)C3H7-i
Figure USRE039607-20070501-C00479
 		150
451 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00480
 		107
452 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00481
 		104
453 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00482
 		100
454 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00483
 		103
455 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00484
 		 95
456 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00485
 		105
457 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00486
 		130
458 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00487
 		100
459 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00488
 		114
460 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00489
 		125
461 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00490
 		143
462 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00491
 		120
463 — O —CF2CHFCl (6-)CH3
Figure USRE039607-20070501-C00492
 		124
464 — O —CF2CHFCl (6-)CH3
Figure USRE039607-20070501-C00493
 		115
465 — O —CF2CHFCl (6-)CH3
Figure USRE039607-20070501-C00494
 		150
466 — O CH3 (3-)CH3
Figure USRE039607-20070501-C00495
 		178
467 — O CH3 (3-)Cl
Figure USRE039607-20070501-C00496
 		188
468 — O C2H5 (3-)Cl
Figure USRE039607-20070501-C00497
 		159
469 — O CH3 (3-)F
Figure USRE039607-20070501-C00498
 		176
470 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00499
 		124
471 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00500
 		 34
472 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00501
 		 68
473 — O C3H7-i (6-)CF3
Figure USRE039607-20070501-C00502
 		 41
474 — O C2H5 (6-)CF3
Figure USRE039607-20070501-C00503
 		127
475 — O H (6-)CF3
Figure USRE039607-20070501-C00504
 		125
476 — S C2H5 (6-)CH3
Figure USRE039607-20070501-C00505
 		214 (Na salt)
477 NH O C2H5 (6-)CH3
Figure USRE039607-20070501-C00506
 		128
478 NH O C2H5 (6-)CH3
Figure USRE039607-20070501-C00507
 		148
479 NH O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00508
 		127
480 NH O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00509
 		 57
481 NH O C2H5 (6-)CH3
Figure USRE039607-20070501-C00510
 		125
482 NH O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00511
 		115
483 NH O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00512
 		151
484 NH O C2H5 (5-)CH3
Figure USRE039607-20070501-C00513
 		132
485 NH O C2H5 (5-)CH3
Figure USRE039607-20070501-C00514
 		106
486 NH O C2H5 (5-)CH3
Figure USRE039607-20070501-C00515
 		163
487 NH O C2H5 (5-)CH3
Figure USRE039607-20070501-C00516
 		137
488 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00517
 		166
489 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00518
 		169
490 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00519
 		130
491 NH O
Figure USRE039607-20070501-C00520
 		(6-)CH3
Figure USRE039607-20070501-C00521
 		148
492 NH O
Figure USRE039607-20070501-C00522
 		(6-)CH3
Figure USRE039607-20070501-C00523
 		138
493 NH O
Figure USRE039607-20070501-C00524
 		(6-)CH3
Figure USRE039607-20070501-C00525
 		147
494 — O
Figure USRE039607-20070501-C00526
 		(6-)CH3
Figure USRE039607-20070501-C00527
 		124
495 — O
Figure USRE039607-20070501-C00528
 		(6-)CH3
Figure USRE039607-20070501-C00529
 		152
496 — O
Figure USRE039607-20070501-C00530
 		(6-)CH3
Figure USRE039607-20070501-C00531
 		141
497 — O
Figure USRE039607-20070501-C00532
 		(6-)CH3
Figure USRE039607-20070501-C00533
 		127
498 — O
Figure USRE039607-20070501-C00534
 		(6-)CH3
Figure USRE039607-20070501-C00535
 		144
499 — O
Figure USRE039607-20070501-C00536
 		(6-)CH3
Figure USRE039607-20070501-C00537
 		107
500 — O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00538
 		265 (Na salt)
501 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00539
 		269 (Na salt)
502 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00540
 		237 (Na salt)
503 — O
Figure USRE039607-20070501-C00541
 		(6-)CH3
Figure USRE039607-20070501-C00542
 		 73
504 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00543
 		220 (Na salt)
505 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00544
 		140
506 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00545
 		120
507 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00546
 		117
508 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00547
 		128
509 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00548
 		232
510 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00549
 		268
511 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00550
 		130
512 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00551
 		137
513 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00552
 		145
514 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00553
 		164
515 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00554
 		 89
516 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00555
 		 86
517 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00556
 		 98
518 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00557
 		122
519 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00558
 		135
520 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00559
 		142
521 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00560
 		157
522 — O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00561
 		126
523 — O C4H9-s (6-)CH3
Figure USRE039607-20070501-C00562
 		140
524 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00563
 		164
525 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00564
 		166
526 — O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00565
 		145
527 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00566
 		239 (Na salt)
528 — O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00567
 		206 (Na salt)
529 — O C2H5 (6-)CH3
Figure USRE039607-20070501-C00568
 		211 (Na salt)
530 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00569
 		166
531 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00570
 		178
532 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00571
 		131
533 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00572
 		130
534 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00573
 		133
535 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00574
 		116
536 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00575
 		192
537 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00576
 		200
538 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00577
 		200
539 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00578
 		105
540 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00579
 		154
541 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00580
 		152
542 — O C3H7-n (6-)C3H7-i
Figure USRE039607-20070501-C00581
 		132
543 — O C3H7-n (6-)C3H7-i
Figure USRE039607-20070501-C00582
 		129
544 — O C3H7-n (6-)C3H7-i
Figure USRE039607-20070501-C00583
 		179
545 — O CH3 (6-)C3H7-i
Figure USRE039607-20070501-C00584
 		174 (Na salt)
546 — O C3H7-n (6-)C3H7-i
Figure USRE039607-20070501-C00585
 		158 (Na salt)
547 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00586
 		200
548 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00587
 		147
549 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00588
 		149
550 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00589
 		136
551 — O C2H5 (6-)C3H7-i
Figure USRE039607-20070501-C00590
 		134
552 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00591
 		175
553 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00592
 		147
554 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00593
 		167
555 — O C3H7-i (6-)C3H7-i
Figure USRE039607-20070501-C00594
 		173
556 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00595
 		188
557 NH O CH3 (6-)CH3
Figure USRE039607-20070501-C00596
 		181
558 NH O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00597
 		136
559 — O CH3 (6-)CH3
Figure USRE039607-20070501-C00598
 		241 (Na salt)
560 NH O C3H7-n (6-)CH3
Figure USRE039607-20070501-C00599
 		129
561 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00600
 		 94
562 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00601
 		 80
563 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00602
 		 68
564 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00603
 		 91
565 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00604
 		123
566 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00605
 		104
567 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00606
 		 90
568 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00607
 		107
569 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00608
 		 70
570 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00609
 		132
571 — S CH3 (6-)OCH3
Figure USRE039607-20070501-C00610
 		150
572 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00611
 		127
573 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00612
 		110
574 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00613
 		130
575 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00614
 		135
576 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00615
 		199 (Na salt)
577 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00616
 		173
578 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00617
 		168
579 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00618
 		125
580 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00619
 		140
581 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00620
 		115
582 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00621
 		111
583 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00622
 		138
584 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00623
 		127
585 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00624
 		142
586 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00625
 		143
587 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00626
 		104
588 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00627
 		118
589 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00628
 		 70
590 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00629
 		110
591 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00630
 		156
592 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00631
 		140
593 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00632
 		148
594 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00633
 		145
595 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00634
 		120
596 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00635
 		100
597 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00636
 		130
598 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00637
 		103
599 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00638
 		104
600 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00639
 		185
601 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00640
 		100
602 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00641
 		138
603 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00642
 		106
604 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00643
 		112
605 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00644
 		140
606 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00645
 		160
607 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00646
 		180
608 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00647
 		142
609 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00648
 		158
610 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00649
 		134
611 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00650
 		140
612 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00651
 		142
613 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00652
 		148
614 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00653
 		146
615 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00654
 		104
616 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00655
 		123
617 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00656
 		123
618 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00657
 		 82
619 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00658
 		 81
620 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00659
 		 88
621 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00660
 		145
622 — S C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00661
 		147
623 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00662
 		205
624 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00663
 		202
625 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00664
 		152
626 — S C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00665
 		168
627 — S C3H7-n (6-)C3H7-n
Figure USRE039607-20070501-C00666
 		145
628 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00667
 		158
629 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00668
 		155
630 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00669
 		145
631 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00670
 		111
632 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00671
 		122
633 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00672
 		171
634 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00673
 		160
635 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00674
 		142
636 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00675
 		106
637 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00676
 		106
638 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00677
 		159
639 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00678
 		148
640 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00679
 		126
641 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00680
 		111
642 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00681
 		171
643 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00682
 		127
644 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00683
 		148
645 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00684
 		123
646 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00685
 		138
647 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00686
 		 95
648 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00687
 		130
649 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00688
 		 74
650 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00689
 		109
651 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00690
 		 75
652 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00691
 		147
653 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00692
 		 99
654 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00693
 		102
655 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00694
 		 98
656 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00695
 		138
657 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00696
 		127
658 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00697
 		160
659 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00698
 		115
660 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00699
 		108
661 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00700
 		154
662 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00701
 		144
663 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00702
 		124
664 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00703
 		138
665 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00704
 		130
666 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00705
 		132
667 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00706
 		100
668 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00707
 		108
669 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00708
 		130
670 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00709
 		133
671 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00710
 		125
672 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00711
 		108
673 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00712
 		110
674 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00713
 		144
675 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00714
 		116
676 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00715
 		139
677 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00716
 		174
678 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00717
 		149
679 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00718
 		104
680 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00719
 		 98
681 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00720
 		112
682 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00721
 		100
683 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00722
 		 92
684 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00723
 		115
685 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00724
 		 99
686 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00725
 		102
687 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00726
 		106
688 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00727
 		120
689 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00728
 		 98
690 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00729
 		138
691 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00730
 		118
692 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00731
 		138
693 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00732
 		 94
694 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00733
 		 94
695 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00734
 		 65
696 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00735
 		 60
697 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00736
 		104
698 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00737
 		104
699 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00738
 		137
700 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00739
 		 70
701 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00740
 		110
702 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00741
 		102
703 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00742
 		137
704 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00743
 		160
705 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00744
 		 94
706 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00745
 		155
707 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00746
 		130
708 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00747
 		142
709 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00748
 		 85
710 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00749
 		106
711 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00750
 		 87
712 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00751
 		120
713 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00752
 		143
714 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00753
 		152
715 — S C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00754
 		112
716 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00755
 		130
717 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00756
 		165
718 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00757
 		161
719 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00758
 		111
720 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00759
 		156
721 — S C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00760
 		137
722 — S CH3 (6-)OCH3
Figure USRE039607-20070501-C00761
 		163
723 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00762
 		113
724 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00763
 		130
725 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00764
 		154
726 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00765
 		157
727 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00766
 		142
728 — S C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00767
 		162
729 — S CH3 (6-)OCH3
Figure USRE039607-20070501-C00768
 		157
730 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00769
 		108
731 — S CH3 (6-)OCH3
Figure USRE039607-20070501-C00770
 		172
732 — S CH3 (6-)OCH3
Figure USRE039607-20070501-C00771
 		147
733 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00772
 		160
734 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00773
 		103
735 — O C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00774
 		172
736 — S C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00775
 		137
737 — S C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00776
 		156
738 — S C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00777
 		103
739 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00778
 		134
740 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00779
 		 87
741 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00780
 		110
742 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00781
 		 88
743 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00782
 		 98
744 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00783
 		 98
745 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00784
 		 88
746 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00785
 		104
747 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00786
 		 75
748 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00787
 		145
749 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00788
 		131
750 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00789
 		158
751 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00790
 		132
752 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00791
 		142
753 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00792
 		130
754 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00793
 		170
755 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00794
 		152
756 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00795
 		138
757 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00796
 		130
758 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00797
 		150
759 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00798
 		156
760 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00799
 		110
761 — S C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00800
 		120
762 — S C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00801
 		104
763 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00802
 		105
764 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00803
 		120
765 — S C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00804
 		135
766 — S C3H7-n (6-)OC3H7-n
Figure USRE039607-20070501-C00805
 		116
767 — S C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00806
 		110
768 — S C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00807
 		 95
769 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00808
 		112
770 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00809
 		 70
771 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00810
 		132
772 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00811
 		 75
773 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00812
 		118
774 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00813
 		 85
775 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00814
 		130
776 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00815
 		120
777 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00816
 		124
778 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00817
 		130
779 — O C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00818
 		100
780 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00819
 		172
781 — O C2H5 (6-)OCH3
Figure USRE039607-20070501-C00820
 		164
782 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00821
 		118
783 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00822
 		 88
784 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00823
 		124
785 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00824
 		100
786 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00825
 		106
787 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00826
 		108
788 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00827
 		105
789 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00828
 		112
790 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00829
 		 80
791 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00830
 		130
792 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00831
 		120
793 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00832
 		 95
794 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00833
 		 96
795 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00834
 		130
796 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00835
 		118
797 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00836
 		134
798 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00837
 		118
799 — O C4H9-s (6-)OC2H5
Figure USRE039607-20070501-C00838
 		 90
800 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00839
 		 78
801 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00840
 		112
802 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00841
 		 78
803 — O C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00842
 		 80
804 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00843
 		 55
805 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00844
 		100
806 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00845
 		 92
807 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00846
 		 74
808 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00847
 		143
809 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00848
 		102
810 — O C3H7-n (6-)OC2H5
Figure USRE039607-20070501-C00849
 		 95
811 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00850
 		 82
812 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00851
 		 92
813 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00852
 		 90
814 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00853
 		124
815 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00854
 		 85
816 — O C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00855
 		 90
817 — O C2H4OC2H5 (6-)OCH3
Figure USRE039607-20070501-C00856
 		 90
818 — O
Figure USRE039607-20070501-C00857
 		(6-)OCH3
Figure USRE039607-20070501-C00858
 		165
819 — O
Figure USRE039607-20070501-C00859
 		(6-)OCH3
Figure USRE039607-20070501-C00860
 		130
820 — O
Figure USRE039607-20070501-C00861
 		(6-)OCH3
Figure USRE039607-20070501-C00862
 		149
821 — O C4H9-s (6-)OC4H9-s
Figure USRE039607-20070501-C00863
 		125
822 — O
Figure USRE039607-20070501-C00864
 		(6-)OCH3
Figure USRE039607-20070501-C00865
 		112
823 — O
Figure USRE039607-20070501-C00866
 		(6-)OCH3
Figure USRE039607-20070501-C00867
 		156
824 — O
Figure USRE039607-20070501-C00868
 		(6-)OCH3
Figure USRE039607-20070501-C00869
 		148
825 — O
Figure USRE039607-20070501-C00870
 		(6-)OCH3
Figure USRE039607-20070501-C00871
 		145
826 — O
Figure USRE039607-20070501-C00872
 		(6-)OCH3
Figure USRE039607-20070501-C00873
 		156
827 — O
Figure USRE039607-20070501-C00874
 		(6-)OCH3
Figure USRE039607-20070501-C00875
 		126
828 — O
Figure USRE039607-20070501-C00876
 		(6-)OCH3
Figure USRE039607-20070501-C00877
 		134
829 — O
Figure USRE039607-20070501-C00878
 		(6-)OCH3
Figure USRE039607-20070501-C00879
 		114
830 — O
Figure USRE039607-20070501-C00880
 		(6-)OCH3
Figure USRE039607-20070501-C00881
 		141
831 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00882
 		125
832 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00883
 		128
833 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00884
 		106
834 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00885
 		 88
835 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00886
 		112
836 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00887
 		125
837 — O C4H9-i (6-)OC2H5
Figure USRE039607-20070501-C00888
 		106
838 — O H (6-)OH
Figure USRE039607-20070501-C00889
 		172
839 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00890
 		102
840 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00891
 		114
841 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00892
 		124
842 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00893
 		 98
843 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00894
 		146
844 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00895
 		 97
845 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00896
 		117
846 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00897
 		142
847 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00898
 		109
848 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00899
 		138
849 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00900
 		135
850 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00901
 		155
851 — S C2H5 (6-)OCH3
Figure USRE039607-20070501-C00902
 		160
852 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00903
 		108
853 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00904
 		143
854 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00905
 		105
855 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00906
 		 65
856 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00907
 		114
857 — O C2H5 (3-)CH3
Figure USRE039607-20070501-C00908
 		179
858 — S C4H9-s (6-)OCH3
Figure USRE039607-20070501-C00909
 		146
859 — S C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00910
 		146
860 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00911
 		132
861 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00912
 		112
862 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00913
 		100
863 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00914
 		138
864 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00915
 		155
865 — S C3H7-i (6-)OC2H5
Figure USRE039607-20070501-C00916
 		140
866 — S C4H9-n (6-)OCH3
Figure USRE039607-20070501-C00917
 		140
867 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00918
 		131
868 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00919
 		135
869 — O C4H9-i (6-)OCH3
Figure USRE039607-20070501-C00920
 		137
870 — O C4H9-n (6-)OC4H9-n
Figure USRE039607-20070501-C00921
 		123
871 — O C4H9-n (6-)OC2H5
Figure USRE039607-20070501-C00922
 		118
872 — O
Figure USRE039607-20070501-C00923
 		(6-)OCH3
Figure USRE039607-20070501-C00924
 		164
873 — O C3H7-i (6-)OCH3
Figure USRE039607-20070501-C00925
 		150
874 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00926
 		148
875 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00927
 		147
876 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00928
 		108
877 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00929
 		108
878 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00930
 		148
879 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00931
 		176
880 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00932
 		144
881 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00933
 		167
882 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00934
 		135
883 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00935
 		100
884 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00936
 		158
885 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00937
 		108
886 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00938
 		164
887 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00939
 		157
888 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00940
 		113
889 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00941
 		132
890 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00942
 		 92
891 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00943
 		141
892 — O C3H7-i (6-)OC3H7-i
Figure USRE039607-20070501-C00944
 		159
893 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00945
 		139
894 — O C2H5 (6-)OC2H5
Figure USRE039607-20070501-C00946
 		150
895 — O C3H7-n (6-)OCH3
Figure USRE039607-20070501-C00947
 		126
896 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00948
 		148
897 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00949
 		157
898 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00950
 		125
899 NH O CH3 (6-)OCH3
Figure USRE039607-20070501-C00951
 		182
900 NH O CH3 (6-)OCH3
Figure USRE039607-20070501-C00952
 		175
901 — O CF3 (6-)CH3
Figure USRE039607-20070501-C00953
 		198 (Na salt)
902 — O CF3 (6-)CH3
Figure USRE039607-20070501-C00954
 		129
903 — O CF3 (6-)CH3
Figure USRE039607-20070501-C00955
 		149
904 — O CF3 (6-)CH3
Figure USRE039607-20070501-C00956
 		163
905 — O CF3 (6-)C2H5
Figure USRE039607-20070501-C00957
 		121
906 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00958
 		170
907 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00959
 		125
908 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00960
 		129
909 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00961
 		156
910 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00962
 		157
911 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00963
 		177
912 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00964
 		172
913 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00965
 		132
914 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00966
 		153
915 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00967
 		150
916 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00968
 		110
917 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00969
 		131
918 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00970
 		133
919 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00971
 		153
920 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00972
 		122
921 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00973
 		147
922 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00974
 		160
923 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00975
 		182
924 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00976
 		142
925 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00977
 		178
926 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00978
 		151
927 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00979
 		178
928 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00980
 		130
929 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00981
 		124
930 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00982
 		153
931 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00983
 		157
932 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00984
 		114
933 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00985
 		130
934 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00986
 		151
935 — O C3H7-i (6-)CH3
Figure USRE039607-20070501-C00987
 		153
936 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00988
 		167
937 — O CF2Cl (6-)CH3
Figure USRE039607-20070501-C00989
 		180 (Na salt)
938 — O CH3 (6-)OCH3
Figure USRE039607-20070501-C00990
 		157 (Na salt)
939 NH O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00991
 		163
940 NH O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C00992
 		160
941 NH O CF2CHFCl (6-)CH3
Figure USRE039607-20070501-C00993
 		 88
942 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00994
 		178
943 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00995
 		135
944 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00996
 		127
945 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00997
 		139
946 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00998
 		280 (Na salt)
947 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C00999
 		171
948 — O CH2CH2F (6-)CH3
Figure USRE039607-20070501-C01000
 		144
949 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01001
 		273 (Na salt)
950 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01002
 		181
951 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01003
 		142
952 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01004
 		114
953 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01005
 		108
954 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01006
 		185
955 — O CH2CHF2 (6-)CH3
Figure USRE039607-20070501-C01007
 		150
956 — O CF3 (6-)C2H5
Figure USRE039607-20070501-C01008
 		143 (Na salt)
957 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01009
 		155
958 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01010
 		112
959 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01011
 		166
960 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01012
 		137
961 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01013
 		132
962 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01014
 		172
963 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01015
 		139
964 — O CF3 (6-)CH3
Figure USRE039607-20070501-C01016
 		130
965 — O C2H5 (3-)CH3
Figure USRE039607-20070501-C01017
 		184
TABLE 1A
Examples of the compounds of the formula (IA)
(IA)
Figure USRE039607-20070501-C01018
Ex. (Position-) Melting
No. A Q R1 R2 Q1 R4 R5 point ° C.
 966 NH O C4H9 (6-)CH3 O
Figure USRE039607-20070501-C01019
 		OC2H5 121
 967 NH O CH2CH(CH3)2 (6-)CH3 O
Figure USRE039607-20070501-C01020
 		OC2H5 127
 968 NH O CH2CF3 (6-)CH3 O CH3 OCH3 164
 969 NH O CH2CF3 (6-)CH3 O CH3 OC2H5 138
 970 NH O CH2CF3 (6-)CH3 O CH3 OC3H7 123
 971 NH O CH2CF3 (6-)CH3 O CH3 OCH(CH3)2 141
 972 — O CH2CH2F (3-)Cl O CH3 OC2H5 139
 973 — O CH2CH2F (3-)CH3 O CH3 OC2H5 154
 974 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01021
 		C4H9-s
 975 — O C3H7-i (6-)CF3 O CH3 C4H9-s
 976 — O C3H7-i (6-)CF3 O CH3 C4H9
 977 — O C3H7-i (6-)CF3 O CH3 C4H9-i
 978 — S C3H7-i (6-)CF3 O CH3 C2H5
 979 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01022
 		OC2H5
 980 — S C3H7 (6-)CH3 O C2H5 OC2H5
 981 — 3 C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01023
 		OC2H5
 982 — S C3H7-i (6-)CH3 O C2H5 OC2H5
 983 — S C3H7 (6-)CH3 O CH3 OC3H7-i
 984 — S C3H7-i (6-)CH3 O CH3 OC3H7-i
 985 — S C3H7 (6-)CH3 O CH3 OC3H7
 986 — S C3H7-i (6-)CH3 O CH3 OC3H7
 987 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01024
 		OCH3
 988 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01025
 		C4H9-s
 989 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01026
 		C4H9-s
 990 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01027
 		C4H9-s
 991 — O CH3 (6-)CF3 O CH3 C4H9-s
 992 — O C2H5 (6-)CF3 O CH3 C4H9-s
 993 — O CH3 (6-)CF3 O CH3 C4H9
 994 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01028
 		C4H9-t
 995 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01029
 		OC3H7
 996 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01030
 		OC3H7
 997 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01031
 		OC3H7
 998 — O C2H5 (6-)CF3 O CH3 C4H9
 999 — O C3H7 (6-)CF3 O CH3 C4H9
1000 — O CH3 (6-)CF3 O CH3 C4H9-i
1001 — S CH3 (6-)CF3 O CH3 SCH3
1002 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01032
 		OC2H5
1003 — S CH3 (6-)CF3 O CH3 OC3H7-i
1004 — S CH3 (6-)CF3 O C2H5 OC2H5
1005 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01033
 		OC3H7
1006 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01034
 		OC3H7-i
1007 — S CH3 (6-)CF3 O CH3 OCH2CF3
1008 — S CH3 (6-)CF3 O CH3 OC3H7
1009 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01035
Figure USRE039607-20070501-C01036
1010 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01037
 		OCH3
1011 — S CH3 (6-)CF3 O
Figure USRE039607-20070501-C01038
 		OCH2CF3
1012 — S CH3 (6-)CH3 O CH3 CH3
1013 — S CH3 (6-)CH3 O CH3 OCH3
1014 — S CH3 (6-)CH3 O CH3 OC2H5
1015 — S CH3 (6-)CH3 O CH3 C2H5
1016 — S C2H5 (6-)CH3 O CH3 C2H5
1017 — S CH3 (6-)CH3 O CH3 SCH3
1018 — S C2H5 (6-)CH3 O CH3 SCH3
1019 — S CH3 (6-)CH3 O
Figure USRE039607-20070501-C01039
 		OC2H5
1020 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01040
 		OC2H5
1021 — S CH3 (6-)CH3 O CH3 OC3H7-i
1022 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01041
 		OC3H7
1023 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01042
 		OCH2CF3
1024 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01043
 		C3H7-i
1025 — O CH3 (6-)CF3 O CH3 C4H9-t
1026 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01044
 		C3H7
1027 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01045
 		C3H7-i
1028 — O CH3 (6-)CF3 O C2H5 C2H5
1029 — O CH3 (6-)CF3 O C3H7 C2H5
1030 — O CH3 (6-)CF3 O C3H7-i C2H5
1031 — O CH3 (6-)CF3 O C2H5 C3H7
1032 — O CH3 (6-)CF3 O C3H7 C3H7
1033 — O CH3 (6-)CF3 O N(CH3)2 CH3
1034 — O CH3 (6-)CF3 O CH3 H
1035 — O CH3 (6-)CF3 O CH3 CH2CH2O
1036 — O CH3 (6-)CF3 O CH3
Figure USRE039607-20070501-C01046
1037 — O CH3 (6-)CF3 O C3H7-i C3H7
1038 — O CH3 (6-)CF3 O C2H5 C3H7-i
1039 — O CH3 (6-)CF3 O C3H7 C3H7-i
1040 — O CH3 (6-)CF3 O C3H7-i C3H7-i
1041 — O CH3 (6-)CF3 O C2H5
Figure USRE039607-20070501-C01047
1042 — O CH3 (6-)CF3 O C3H7
Figure USRE039607-20070501-C01048
1043 — O CH3 (6-)CF3 O C3H7-i
Figure USRE039607-20070501-C01049
1044 — O C2H5 (6-)CF3 O C3H7-i
Figure USRE039607-20070501-C01050
1045 — O C3H7 (6-)CF3 O C3H7-i
Figure USRE039607-20070501-C01051
1046 — O CH3 (6-)CF3 O CH3 OCH2CF2CHF2
1047 — O C3H7 (6-)CF3 O CH3 OCH2CF2CHF2
1048 — O CH3 (6-)CF3 O CH3 OC6H11
1049 — O C2H5 (6-)CF3 O CH3 OC6H11
1050 — O C3H7 (6-)CF3 O CH3 OC6H11
1051 — O CH3 (6-)CF3 O CH3
Figure USRE039607-20070501-C01052
1052 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01053
 		C4H9-i
1053 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01054
 		C4H9
1054 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01055
 		CH3
1055 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01056
 		C2H5
1056 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01057
Figure USRE039607-20070501-C01058
1057 — O CH3 (6-)CF3 O C2H5 CH3
1058 — O C3H7-i (6-)CF3 O C3H7-i
Figure USRE039607-20070501-C01059
1059 — O C3H7-i (6-)CF3 O CH3 OCH2CF2CHF2
1060 — O C3H7 (6-)CF3 O CH3 CH3
1061 — O C3H7 (6-)CF3 O CH3 C3H7-i
1062 — O C3H7 (6-)CF3 O CH3 CH2OCH3
1063 — O C3H7 (6-)CF3 O CH3 Br
1064 — O C2H5 (6-)CF3 O CH3 OCH2CF3
1065 — O C3H7 (6-)CF3 O OCH3 C3H7
1066 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01060
 		Br
1067 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01061
 		CH2OCH3
1068 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01062
 		CH2OCH3
1069 — S C2H5 (6-)CF3 O CH3 SCH3
1070 — S C3H7 (6-)CF3 O CH3 SCH3
1071 — S C3H7-i (6-)CF3 O CH3 SCH3
1072 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01063
 		OC2H5
1073 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01064
 		OC2H5
1074 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01065
 		OC2H5
1075 — S C2H5 (6-)CF3 O CH3 OC3H7-i
1076 — S C3H7 (6-)CF3 O CH3 OC3H7-i
1077 — S C3H7-i (6-)CF3 O CH3 OC3H7-i
1078 — S C2H5 (6-)CF3 O C2H5 OC2H5
1079 — S C3H7 (6-)CF3 O C2H5 OC2H5
1080 — S C3H7-i (6-)CF3 O C2H5 OC2H5
1081 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01066
 		OC3H7
1082 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01067
 		OC3H7
1083 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01068
 		OC3H7
1084 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01069
 		C4H9-t
1085 — O C2H5 (6-)CF3 O CH3 OC4H9-s
1086 — O C3H7 (6-)CF3 O CH3
Figure USRE039607-20070501-C01070
1087 — O C3H7-i (6-)CF3 O CH3 OC4H9-s
1088 — O C2H5 (6-)CF3 O CH3 OC6H5
1089 — O C3H7 (6-)CF3 O CH3 OC6H5
1090 — O C3H7-i (6-)CF3 O CH3 OC6H5
1091 — O C2H5 (6-)CF3 O CH2CH═CH2 OCH2CF3
1092 — O C3H7 (6-)CF3 O CH2CH═CH2 OCH2CF3
1093 — O C3H7-i (6-)CF3 O CH2CH═CH2 OCH2CF3
1094 — O C2H5 (6-)CF3 O CH3 OCH2C6H5
1095 — O C3H7 (6-)CF3 O CH3 OCH3C6H5
1096 — O C3H7-i (6-)CF3 O CH3 OCH2C6H5
1097 — O C2H5 (6-)CF3 O N(CH3)2 CH3
1098 — O C3H7 (6-)CF3 O N(CH3)2 CH3
1099 — O C3H7-i (6-)CF3 O N(CH3)2 CH3
1100 — O C3H7 (6-)CF3 O CH3 H
1101 — O C2H5 (6-)CF3 O CH3 CH2CH2OC3H7-i
1102 — O C3H7-i (6-)CF3 O CH3 CH2CH2OC3H7-i
1103 — O C2H5 (6-)CF3 O CH3
Figure USRE039607-20070501-C01071
1104 — O C3H7 (6-)CF3 O CH3
Figure USRE039607-20070501-C01072
1105 — O C3H7-i (6-)CF3 O CH3
Figure USRE039607-20070501-C01073
1106 — O C2H5 (6-)CF3 O CH3 OCH2CF2CHF2
1107 — S C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01074
 		OCH3
1108 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01075
 		OC3H7-i
1109 — S C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01076
 		OC3H7-i
1110 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01077
 		OC3H7
1111 — S C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01078
 		OC3H7
1112 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01079
 		C4H9-i
1113 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01080
 		C4H9-i
1114 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01081
 		C4H9-i
1115 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01082
 		C4H9
1116 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01083
 		C4H9
1117 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01084
 		C4H9
1118 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01085
 		CH3
1119 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01086
 		CH3
1120 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01087
 		CH3
1121 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01088
 		C2H5
1122 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01089
 		C2H5
1123 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01090
 		C2H5
1124 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01091
Figure USRE039607-20070501-C01092
1125 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01093
Figure USRE039607-20070501-C01094
1126 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01095
Figure USRE039607-20070501-C01096
1127 — O C2H5 (6-)CF3 O C3H7
Figure USRE039607-20070501-C01097
1128 — O C3H7 (6-)CF3 O C3H7
Figure USRE039607-20070501-C01098
1129 — O C3H7-i (6-)CF3 O C3H7
Figure USRE039607-20070501-C01099
1130 — O C2H5 (6-)CF3 O C2H5 CH3
1131 — O C3H7 (6-)CF3 O C2H5 CH3
1132 — O C3H7-i (6-)CF3 O C2H5 CH3
1133 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01100
 		C3H7
1134 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01101
 		C3H7
1135 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01102
 		C3H7
1136 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01103
 		C3H7-i
1137 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01104
 		C3H7-i
1138 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01105
 		C3H7-i
1139 — O C2H5 (6-)CF3 O C2H5 C2H5
1140 — O C3H7 (6-)CF3 O C2H5 C2H5
1141 — O C3H7-i (6-)CF3 O C2H5 C2H5
1142 — O C2H5 (6-)CF3 O C3H7 C2H5
1143 — O C3H7 (6-)CF3 O C3H7 C2H5
1144 — O C3H7-i (6-)CF3 O C3H7 C2H5
1145 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01106
 		OC3H7-i
1146 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01107
 		OC3H7-i
1147 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01108
 		OC3H7-i
1148 — S C2H5 (6-)CF3 O CH3 OCH2CF3
1149 — S C3H7 (6-)CF3 O CH3 OCH2CF3
1150 — S C3H7-i (6-)CF3 O CH3 OCH2CF3
1151 — S C2H5 (6-)CF3 O CH3 OC3H7
1152 — S C3H7 (6-)CF3 O CH3 OC3H7
1153 — S C3H7-i (6-)CF3 O CH3 OC3H7
1154 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01109
Figure USRE039607-20070501-C01110
1155 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01111
Figure USRE039607-20070501-C01112
1156 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01113
Figure USRE039607-20070501-C01114
1157 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01115
 		OCH3
1158 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01116
 		OCH3
1159 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01117
 		OCH3
1160 — S C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01118
 		OCH2CF3
1161 — S C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01119
 		OCH2CF3
1162 — S C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01120
 		OCH2CF3
1163 — O C2H5 (6-)CF3 O C3H7-i C3H7
1164 — O C3H7 (6-)CF3 O C3H7-i C3H7
1165 — O C3H7-i (6-)CF3 O C3H7-i C3H7
1166 — O C2H5 (6-)CF3 O C2H5 C3H7-i
1167 — O C3H7 (6-)CF3 O C2H5 C3H7-i
1168 — O C3H7-i (6-)CF3 O C2H5 C3H7-i
1169 — O C2H5 (6-)CF3 O C3H7 C3H7-i
1170 — O C3H7 (6-)CF3 O C3H7 C3H7-i
1171 — O C3H7-i (6-)CF3 O C3H7 C3H7-i
1172 — O C2H5 (6-)CF3 O C3H7-i C3H7-i
1173 — O C3H7 (6-)CF3 O C3H7-i C3H7-i
1174 — O C3H7-i (6-)CF3 O C3H7-i C3H7-i
1175 — O C2H5 (6-)CF3 O C3H7-i C2H5
1176 — O C3H7 (6-)CF3 O C3H7-i C2H5
1177 — O C3H7-i (6-)CF3 O C3H7-i C2H5
1178 — O C2H5 (6-)CF3 O C2H5 C3H7
1179 — O C3H7 (6-)CF3 O C2H5 C3H7
1180 — O C3H7-i (6-)CF3 O C2H5 C3H7
1181 — O C2H5 (6-)CF3 O C3H7 C3H7
1182 — O C3H7 (6-)CF3 O C3H7 C3H7
1183 — O C3H7-i (6-)CF3 O C3H7 C3H7
1184 — O C2H5 (6-)CF3 O CH3 C4H9-t
1185 — O C3H7 (6-)CF3 O CH3 C4H9-t
1186 — O C3H7-i (6-)CF3 O CH3 C4H9-t
1187 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01121
 		C4H9-t
1188 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01122
 		C4H9-t
1189 — O C2H5 (6-)CF3 O C2H5
Figure USRE039607-20070501-C01123
1190 — O C3H7 (6-)CF3 O C2H5
Figure USRE039607-20070501-C01124
1191 — O C3H7-i (6-)CF3 O C2H5
Figure USRE039607-20070501-C01125
1192 — O C3H7-i (6-)CF3 O CH3 OC6H11
1193 — S C3H7 (6-)CH3 O CH3 OCH2CF3
1194 — S C3H7-i (6-)CH3 O CH3 OCH2CF3
1195 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01126
 		OCH2CF3
1196 — S C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01127
 		OCH2CF3
1197 — S C3H7-i (6-)CH3 O CH3 C2H5
1198 — S CH3 (6-)CF3 O CH3 C2H5
1199 — S C2H5 (6-)CF3 O CH3 C2H5
1200 — S C3H7 (6-)CF3 O CH3 C2H5
1201 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01128
 		H
1202 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01129
 		H
1203 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01130
 		H
1204 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01131
 		H
1205 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01132
 		OCH3
1206 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01133
 		OCH3
1207 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01134
 		OCH3
1208 — O CH3 (6-)CF3 O CH2CH═CH2 OC3H7
1209 — O C2H5 (6-)CF3 O CH2CH═CH2 OC3H7
1210 — O CH3 (6-)CF3 O CH3 OCH2C4H9-t
1211 — O C2H5 (6-)CF3 O CH3 OCH2C4H9-t
1212 — O C3H7 (6-)CF3 O CH3 OCH2C4H9-t
1213 — O C3H7-i (6-)CF3 O CH3 OCH2C4H9-t
1214 — O CH3 (6-)CF3 O CH3 OCH2CCl3
1215 — O C2H5 (6-)CF3 O CH3 OCH2CCl3
1216 — O C3H7 (6-)CF3 O CH3 OCH2CCl3
1217 — O C3H7-i (6-)CF3 O CH3 OCH2CCl3
1218 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01135
 		CH═CHCH3
1219 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01136
 		CH═CHCH3
1220 — O CH3 (4-)CH3 O CH3 OCH3
1221 — O CH3 (4-)CH3 O CH3 OC2H5
1222 — O CH3 (4-)CH3 O
Figure USRE039607-20070501-C01137
 		OC2H5
1223 — O CH3 (4-)CH3 O
Figure USRE039607-20070501-C01138
 		OC3H7
1224 — O CH3 (4-)CH3 O CH3 OC3H7
1225 — O CH3 (4-)CH3 O
Figure USRE039607-20070501-C01139
 		OCH3
1226 — O CH3 (6-)CF3 O CH3 OCH2C6H5
1227 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01140
 		CH═CHCH3
1228 — O CH3 (6-)CF3 O CH3 CH2CH2OCH3
1229 — O C2H5 (6-)CF3 O CH3 CH2CH2OCH3
1230 — O C2H5 (6-)CF3 O
Figure USRE039607-20070501-C01141
 		CH═CHCH3
1231 — O C3H7 (6-)CF3 O
Figure USRE039607-20070501-C01142
 		CH═CHCH3
1232 — O C3H7-i (6-)CF3 O CH3 CH2CH2OCH3
1233 — O C3H7-i (6-)CF3 O
Figure USRE039607-20070501-C01143
 		CH═CHCH3
1234 — S CH3 (6-)CH3 O
Figure USRE039607-20070501-C01144
 		OC3H7-i
1235 — S CH3 (6-)CH3 O CH3 OCH2CF3
1236 — S CH3 (6-)CH3 O CH3 OC3H7
1237 — S CH3 (6-)CH3 O
Figure USRE039607-20070501-C01145
 		OCH3
1238 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01146
 		OC3H7-i
1239 — S C2H5 (6-)CH3 O CH3 OCH2CF3
1240 — S C2H5 (6-)CH3 O CH3 OC3H7
1241 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01147
 		OCH3
1242 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01148
 		OCH2CF3
1243 — S CH3 (6-)CH3 O
Figure USRE039607-20070501-C01149
1244 — S C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01150
1245 — S C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01151
1246 — S C3H7-i (6-)CH3 O
Figure USRE039607-20070501-C01152
1247 — O CH3 (6-)CF3 O
Figure USRE039607-20070501-C01153
 		OCH3
1248 — O CH2CH2F (6-)CF3 O CH3 OCH3
1249 — O CH2CH2F (6-)CF3 O CH3 OC2H5
1250 — O CH2CH2F (6-)CF3 O
Figure USRE039607-20070501-C01154
 		OC2H5
1251 — O CH2CH2F (6-)CF3 O CH3 OC3H7
1252 — O CH2CH2F (6-)CF3 O CH3 OC3H7-i
1253 — O CH2CH2F (6-)CF3 O
Figure USRE039607-20070501-C01155
 		OC3H7
1254 — O CH2CH2F (6-)CF3 O
Figure USRE039607-20070501-C01156
 		OC3H7-i
1255 — O CH2CH2F (6-)CF3 O
Figure USRE039607-20070501-C01157
1256 — O CH3 (6-)C2H5 O CH3 CH2OCH3 124
1257 — O CH3 (6-)C2H5 O CH3 OCH2CF3 156
1258 — O CH3 (6-)C2H5 O CH3 SC═CH 147
1259 — O CH3 (6-)C2H5 O CH3 CH(CH3)2 113
1260 — O CH3 (6-)C2H5 O CH3 CH(CH3)2 125
1261 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01158
 		Br 154
1262 — O CH3 (6-)C2H5 O C2H5 OC2H5 >250
1263 — O CH3 (6-)C2H5 O CH3 OC3H7 200
1264 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01159
 		OC2H5 178
1265 — O CH3 (6-)Br O CH3 OC2H5 228
1266 — O C2H5 (6-)C2H5 O C2H5 OC2H5
1267 — O C2H5 (6-)C2H5 O CH3 OC3H7
1268 — O CH(CH3)2 (6-)C2H5 O C2H5 OC2H5
1269 — O CH(CH3)2 (6-)C2H5 O CH3 OC3H7
1270 — O C2H5 (6-)C2H5 O CH3 CH2OCH3
1271 — O C2H5 (6-)C2H5 O CH3 OCH2CF3
1272 — O CH(CH3)2 (6-)C2H5 O CH3 CH2OCH3
1273 — O CH(CH3)2 (6-)C2H5 O CH3 OCH2CF3
1274 — O CF3 (6-)Br O CH3 OC2H5
1275 — O C2H5 (6-)C2H5 O CH3 OCH(CH3)2
1276 — O C2H5 (6-)C2H5 O
Figure USRE039607-20070501-C01160
 		OC2H5
1277 — O C2H5 (6-)C2H5 O
Figure USRE039607-20070501-C01161
 		CH2OCH3
1278 — O CH(CH3)2 (6-)C2H5 O CH3 OCH(CH3)2
1279 — O CH(CH3)2 (6-)C2H5 O OC2H5
1280 — O CH(CH3)2 (6-)C2H5 O
Figure USRE039607-20070501-C01162
 		CH2OCH3
1281 — O C3H7 (6-)Br O CH3 OC2H5
1282 — O C2H5 (6-)C2H5 O CH3 OCH3
1283 — O C2H5 (6-)F O CH3 OC2H5 165
1284 — O CH3 (6-)F O CH3 OC2H5 211
1285 — O CH3 (6-)CN O CH3 OC2H5 255
1286 — O CH3 (6-)CN O CH3 OC2H5
1287 — O CH3 (6-)CN O CH3 C2H5 162
1288 — O CH3 (6-)CN O CH3 SCH3 268
1289 — O CH3 (6-)CN O CH3 OCH3 242
1290 — O CH3 (6-)CH(CH3)2 O CH3 OCH3 183
1291 — O C2H5 (6-)CH(CH3)2 O CH3 CH3 283
1292 — O C2H5 (6-)CH(CH3)2 O CH3 OCH3 227
1293 — O CH3 (6-)F O CH3 OC2H5
1294 — O CH3 (6-)F O CH3 C2H5 156
1295 — O CH3 (6-)F O CH3 CH3 179
1296 — O CH3 (6-)F O CH3 CH3 217
1297 — O CH3 (6-)F O
Figure USRE039607-20070501-C01163
 		OCH(CH3)2 147
1298 — O CH(CH3)2 (6-)F O CH3 OC2H5 165
1299 — O CH(CH3)2 (6-)F O CH3 C2H5 113
1300 — O CH(CH3)2 (6-)F O CH3 OCH3 149
1301 — O CH(CH3)2 (6-)F O
Figure USRE039607-20070501-C01164
 		CH3 147
1302 — O CH(CH3)2 (6-)F O
Figure USRE039607-20070501-C01165
 		OCH(CH3)2 127
1303 — O C3H7 (6-)F O CH3 OC2H5 139
1304 — O C3H7 (6-)F O CH3 C2H5 116
1305 — O C3H7 (6-)F O CH3 OCH3 129
1306 — O C3H7 (6-)F O
Figure USRE039607-20070501-C01166
 		CH3 120
1307 — O C3H7 (6-)F O CH3 OC2H5 >160
1308 — O C2H5 (6-)CH3 O CH3 OC4H9 114
1309 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01167
 		OC4H9 126
1310 — O C2H5 (6-)CH3 O CH3 OCH2CH(CH3)2 144
1311 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01168
 		OCH2CH(CH3)2 145
1312 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01169
 		OCH2CF3 133
1313 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01170
 		OCH3 181
1314 — O C2H5 (6-)CH(CH3)2 O CH3 OC4H9 170
1315 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01171
 		OC4H9 129
1316 — O CH3 (6-)CH3 O CH3 OCH2CH(CH3)2 137
1317 — O CH3 (6-)CH3 O
Figure USRE039607-20070501-C01172
 		OCH2CH(CH3)2 165
1318 — O CH3 (6-)CH3 O CH3
Figure USRE039607-20070501-C01173
 		150
1319 — O CH3 (6-)CH3 O
Figure USRE039607-20070501-C01174
Figure USRE039607-20070501-C01175
 		186
1320 — O C2H5 (6-)CH(CH3)2 O CH3 OCH2CH(CH3)2 163
1321 — O C2H5 (6-)CH(CH3)2 O CH3
Figure USRE039607-20070501-C01176
 		134
1322 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01177
Figure USRE039607-20070501-C01178
 		187
1323 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01179
 		CH3 158
1324 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01180
 		C2H5 172
1325 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01181
 		C3H7 142
1326 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01182
 		OCH2CF3 150
1327 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01183
 		OCH3 137
1328 — O C2H5 (6-)CH(CH3)2 O
Figure USRE039607-20070501-C01184
 		CH(CH3)2 168
1329 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01185
 		SCH3 167
1330 — O CH(CH3)2 (6-)CH3 O
Figure USRE039607-20070501-C01186
 		SCH3 167
1331 — O C2H5 (6-)CH3 O
Figure USRE039607-20070501-C01187
 		SC2H5 150
1332 — O CH(CH3)2 (6-)CH3 O
Figure USRE039607-20070501-C01188
 		SC2H5 150
1333 — O C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01189
 		SC2H5 140
1334 — O C2H5 (6-)F O CH3 SCH3 165
1335 — O C2H5 (6-)F O CH3 C2H5 135
1336 — O C2H5 (6-)F O CH3 OCH3 168
1337 — O C2H5 (6-)F O CH3 CH3 140
1338 — O C2H5 (6-)F O
Figure USRE039607-20070501-C01190
 		OCH3 138
1339 — O C3H7 (6-)OC3H7 O CH3 OC2H5
1340 — O C3H7 (6-)OC3H7 O CH3 OC2H5
1341 — O C3H7 (6-)OCH3 O CH3 OC2H5
1342 — O CH(CH3)2 (6-)OCH(CH3)2 O CH3 OC2H5
1343 — O C2H5 (6-)OC2H5 O CH3 OC2H5
1344 — O C4H9 (6-)OC4H9 O CH3 OC2H5
1345 — O CH(CH3)C2H5 (6-)OCH3 O CH3 CH3 157
1346 — O CH(CH3)C2H5 (6-)OCH3 O CH3 C3H7 86
1347 — O CH2CH(CH3)2 (6-)OC2H5 O CH3 Br 108
1348 — O CH2CH(CH3)2 (6-)OC2H5 O CH3 CH3 82
1349 — O CH2CH(CH3)2 (6-)OC2H5 O
Figure USRE039607-20070501-C01191
 		Br 120
1350 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01192
 		OCH(CH3)2 141
1351 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01193
 		OC3H7 102
1352 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01194
 		OCH(CH3)2 110
1353 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01195
 		OC3H7 132
1354 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01196
 		OCH2CF3 114
1355 — O CH(CH3)2 (6-)OCH3 O
Figure USRE039607-20070501-C01197
 		OCH(CH3)2 172
1356 — O CH(CH3)2 (6-)OCH3 O
Figure USRE039607-20070501-C01198
 		OC3H7 156
1357 — O C3H7 (6-)OC3H7 O
Figure USRE039607-20070501-C01199
 		OCH(CH3)2 141
1358 — O C2H5 (6-)OCH3 O
Figure USRE039607-20070501-C01200
 		OC3H7 134
1359 — O C2H5 (6-)OC3H7 O
Figure USRE039607-20070501-C01201
 		OCH(CH3)2 132
1360 — O CH(CH3)2 (6-)OC2H5 O
Figure USRE039607-20070501-C01202
 		OCH(CH3)2 147
1361 — O (CH2)2OC3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01203
 		OCH2CF3 134
1362 — O CH2CH(CH3)2 (6-)OC2H5 O
Figure USRE039607-20070501-C01204
 		OCH(CH3)2 96
1363 — O C3H7 (6-)OC2H5 O
Figure USRE039607-20070501-C01205
 		OCH3 120
1364 — O CH(CH3)2 (6-)OC2H5 O
Figure USRE039607-20070501-C01206
 		OCH3 108
1365 — O CH(CH3)2 (6-)OC2H5 O
Figure USRE039607-20070501-C01207
 		OC3H7 127
1366 — O C4H9 (6-)OC4H9 O
Figure USRE039607-20070501-C01208
 		OCH3 118
1367 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01209
 		154
1368 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01210
 		CH3 122
1369 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01211
 		CH3 134
1370 — O CH(CH3)2 (6-)OCH(CH3)2 O CH3 CH(CH3)C2H5 97
1371 — O C3H7 (6-)OCH3 O CH3 CH(CH3)2 76
1372 — O C3H7 (6-)OCH3 O CH3 SC2H5 91
1373 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01212
Figure USRE039607-20070501-C01213
 		102
1374 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01214
 		CH3 125
1375 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01215
 		C2H5 112
1376 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01216
 		C3H7 113
1377 — O C2H5 (6-)OC2H5 O CH3 CH(CH3)C2H5 100
1378 — O C2H5 (6-)OC2H5 O CH3 CH(CH3)2 118
1379 — O C2H5 (6-)OC2H5 O CH3 C4H9 81
1380 — O C2H5 (6-)OC2H5 O CH3 CH2CH(CH3)2 93
1381 — O C3H7 (6-)OCH3 O CH3 CH(CH3)C2H5 79
1382 — O C3H7 (6-)OCH3 O CH3 CH2CH(CH3)2 83
1383 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01217
 		OC2H5 67
1384 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01218
 		C3H7 105
1385 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01219
 		OCH(CH3)2 97
1386 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01220
 		OCH(CH3)2 82
1387 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01221
 		CH2CH(CH3)2 103
1388 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01222
 		CH2CH(CH3)2 116
1389 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01223
 		OCH3 104
1390 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01224
 		OCH3 127
1391 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01225
 		OCH3 93
1392 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01226
 		OC3H7 107
1393 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01227
 		OC3H7 130
1394 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01228
 		OC3H7 80
1395 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01229
 		C4H9 77
1396 — O C3H7 (6-)CH3 O
Figure USRE039607-20070501-C01230
 		C4H9 107
1397 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01231
Figure USRE039607-20070501-C01232
 		107
1398 — O C3H7 (6-)OCH3 O
Figure USRE039607-20070501-C01233
Figure USRE039607-20070501-C01234
 		85
1399 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01235
 		C4H9 89
1400 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01236
Figure USRE039607-20070501-C01237
 		100
1401 — O CH(CH3)2 (6-)OCH(CH3)2 O CH3 CH(CH3)2 118
1402 — O CH(CH3)2 (6-)OCH(CH3)2 O CH3 C4H9 82
1403 — O C3H7 (6-)OCH3 O CH3 C4H9 75
1404 — O CH(CH3)2 (6-)OCH(CH3)2 O
Figure USRE039607-20070501-C01238
 		CH2CH(CH3)2 95
1405 — O C2H5 (6-)OC2H5 O CH3 C(CH3)═CH2 118
1406 — O CH(CH3)2 (6-)OCH(CH3)2 O CH3 C(CH3)═CH2 103
1407 — O C3H7 (6-)OCH3 O CH3 C(CH3)═CH2 92
1408 — O C3H7 (6-)OH O CH3 OC2H5 152
1409 — O C3H7 (6-)OH O CH3 OCH3 137
1410 — O C3H7 (6-)OH O CH3 OC3H7 88
1411 — O C3H7 (6-)OH O CH3 OCH(CH3)2 125
1412 — O CH3 (6-)OH O CH3 OCH3 148
1413 — O CH3 (6-)OH O CH3 OC2H5 144
1414 — O CH3 (6-)OH O CH3 OC3H7 128
1415 — O CH3 (6-)OH O CH3 OCH(CH3)2 158
1416 — O CH3 (6-)OH O
Figure USRE039607-20070501-C01239
 		OCH(CH3)2 137
1417 — O CH3 (6-)OH O
Figure USRE039607-20070501-C01240
 		OC2H5 125
1418 — O CH3 (6-)OH O C2H5 OCH3 137
1419 — O CH3 (6-)OH O CH3 SCH3 130
1420 — O CH3 (6-)OH O CH3 C2H5 40
1421 — O C3H7 (6-)OCHF2 O CH3 OC2H5 230
1422 — O CH3 (6-)OCHF2 O CH3 OC2H5 202
1423 — O CH3 (6-)OCHF2 O CH3 SCH3 202
1424 — O CH3 (6-)OCHF2 O CH3 C2H5 98
1425 — S C3H7 (6-)OCHF2 O CH3 OC3H7 198
1426 — O C3H7 (6-)OCHF2 O
Figure USRE039607-20070501-C01241
 		OC2H5 124
1427 — O CHF2 (6-)OCRF2 O CH3 OCH3 145
1428 — O CHF2 (6-)OCHF2 O CH3 OC2H5 177
1429 — O CHF2 (6-)OCHF2 O CH3 OC2H5 >220
1430 — O CHF2 (6-)OCHF2 O
Figure USRE039607-20070501-C01242
 		OC2H5 148
1431 — O CHF2 (6-)OCHF2 O CH3 C2H5 123
1432 — O CHF2 (6-)OCHF2 O CH3 SCH3 133
1433 — O CHF2 (6-)OCHF2 O
Figure USRE039607-20070501-C01243
 		CH(CH3)2 130
1434 — O C3H7 (6-)OCHF2 O CH3 OCH(CH3)2
1435 — O CH2CH═CH2 (6-)OC2H5 O
Figure USRE039607-20070501-C01244
 		OC2H5 84
1436 — O CH2CH═CH2 (6-)OC2H5 O
Figure USRE039607-20070501-C01245
 		OCH3 120
1437 — O CH2CH═CH2 (6-)OC2H5 O CH3 OCH(CH3)2 133
1438 — O CH2CH═CH2 (6-)OC2H5 O CH3 C2H5 137
1439 — O CH2CH═CH2 (6-)OC2H5 O CH3 OC2H5 100
1440 — O CH2CH═CH2 (6-)OC2H5 O CH3 OCH3 94
1441 — O CH3 (6-)OCH3 O CH3 N(CH3)2 168
1442 — O CH3 (6-)C2H5 O CH3 N(CH3)2 172
1443 — O CF3 (6-)C2H5 O CH3 N(CH3)2 128
1444 — O CF3 (6-)CH3 O CH3 OC2H5 224
1445 — O CH3 (6-)OCH3 O OCH3 SCH3 157
1446 — O CH3 (6-)OCH3 O OCH3 SC2H5 149
1447 — O CH3 (6-)OCH3 O OC2H5 SCH3 147
1448 — O CH3 (6-)OCH3 O OC2H5 SC2H5 124
1449 — O CH3 (6-)C2H5 O NH2 CH3 204
1450 — O C2H5 (6-)OC2H5 O OCH3 SCH3 130
1451 — O C2H5 (6-)OC2H5 O OCH3 SC2H5 112
1452 — O C2H5 (6-)OC2H5 O OC2H5 SCH3 113
1453 — O OC2H5 (6-)OC2H5 O OC2H5 SC2H5 157
1454 — O CF2CF2H (6-)CH3 O CH3 OCH3 127
1455 — O CF2CF2H (6-)CH3 O CH3 OC2H5 156
1456 — O CF2CF2H (6-)CH3 O CH3 OC3H7 132
1457 — O CF2CF2H (6-)CH3 O CH3 OCH(CH3)2 172
1458 — O CF2CF2H (6-)CH3 O CH3 C3H7 90
1459 — O CF3 (6-)C2H5 O CH3 OC3H7 185
1460 — O CF3 (6-)C2H5 O CH3 OCH(CH3)2 192
1461 — O CF3 (6-)C2H5 O CH3 OCH2CF3 159
1462 — O CF3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01246
 		192
1463 — O CF3 (6-)C2H5 O CH3 CH3 >270
1464 — O CF3 (6-)C2H5 O CH3 C2H5 259
1465 — O CF3 (6-)C2H5 O CH3 C3H7 241
1466 — O CF3 (6-)C2H5 O CH3 SCH3 174
1467 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01247
 		OCH3 165
1468 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01248
 		OC2H5 145
1469 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01249
 		OC3H7 196
1470 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01250
 		OCH(CH3)2 170
1471 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01251
 		OCH2CF3 183
1472 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01252
Figure USRE039607-20070501-C01253
 		154
1473 — O CF3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01254
 		188
1474 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01255
 		C2H5 163
1475 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01256
 		C3H7 190
1476 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01257
 		SCH3 159
1477 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01258
 		CH3 151
1478 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01259
 		C3H7 163
1479 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01260
 		CH═CH(CH3) 176
1480 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01261
Figure USRE039607-20070501-C01262
 		156
1481 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01263
 		CH2OCH3 146
1482 — O CH3 (6-)C2H5 O OCH3 SCH3 149
1483 — O CH3 (6-)C2H5 O OCH3 SC2H5 137
1484 — O CH3 (6-)C2H5 O OC2H5 SCH3 115
1485 — O CH3 (6-)C2H5 O OC2H5 SC2H5 99
1486 — O CH(CH3)2 (6-)CH3 O
Figure USRE039607-20070501-C01264
 		CH(CH3)2 132
1487 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01265
 		CH(CH3)2 108
1488 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01266
 		CH(CH3)2 151
1489 — O CH3 (6-)OCH3 O
Figure USRE039607-20070501-C01267
 		CH(CH3)2 163
1490 — O C2H5 (6-)OC2H5 O
Figure USRE039607-20070501-C01268
 		CH(CH3)2 111
1491 — O CH3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01269
 		118
1492 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01270
Figure USRE039607-20070501-C01271
 		147
1493 — O CF3CF3H (6-)CH3 O
Figure USRE039607-20070501-C01272
 		OCH3 160
1494 — O CF3CF3H (6-)CH3 O
Figure USRE039607-20070501-C01273
 		OC2H5 155
1495 — O CF3CF3H (6-)CH3 O
Figure USRE039607-20070501-C01274
 		OCH(CH3)2 149
1496 — O CH2CF3 (6-)CH3 O CH3 OCH3 149
1497 — O CH2CF3 (6-)CH3 O CH3 OC2H5 230
1498 — O CH2CF3 (6-)CH3 O CH3 OC3H7 238
1499 — O CH2CF3 (6-)CH3 O CH3 OCH(CH3)2 89
1500 — O CH2CF3 (6-)CH3 O CH3
Figure USRE039607-20070501-C01275
 		134
1501 — O CH2CF3 (6-)CH3 O
Figure USRE039607-20070501-C01276
 		OCH3 189
1502 — O CH2CF3 (6-)CH3 O
Figure USRE039607-20070501-C01277
 		OC2H5 129
1503 — O CH2CF3 (6-)CH3 O
Figure USRE039607-20070501-C01278
 		OC3H7 126
1504 — O CH2CF3 (6-)CH3 O
Figure USRE039607-20070501-C01279
 		OCH(CH3)2 161
1505 — O CH2CF3 (6-)CH3 O
Figure USRE039607-20070501-C01280
Figure USRE039607-20070501-C01281
 		128
1506 — O CH2CF3 (6-)CH3 O CH3 C3H7 148
1507 — O CH3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01282
 		144
1508 — O CH3 (6-)C2H5 O CH3 CH═CH(CH3) 138
1509 — O CH3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01283
 		160
1510 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01284
 		CH3 168
1511 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01285
 		C2H5 143
1512 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01286
 		C3H7 140
1513 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01287
Figure USRE039607-20070501-C01288
 		170
1514 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01289
 		CH═CH(CH3) 127
1515 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01290
 		N(CH3)2 214
1516 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01291
 		SCH3 167
1517 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01292
 		SC2H5 137
1518 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01293
 		OCH3 165
1519 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01294
 		OCH2CF3 163
1520 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01295
 		OC2H7 125
1521 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01296
Figure USRE039607-20070501-C01297
 		133
1522 — O CH3 (6-)C2H5 O CH3
Figure USRE039607-20070501-C01298
 		136
1523 — O CF2H (6-)C2H5 O CH3 OCH3 121
1524 — O CF2H (6-)C2H5 O CH3 OC2H5 150
1525 — O CF2H (6-)C2H5 O CH3 OC3H7 119
1526 — O CF2H (6-)C2H5 O CH3 OCH(CH3)2 122
1527 — O CF2H (6-)C2H5 O CH3
Figure USRE039607-20070501-C01299
 		146
1528 — O CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01300
 		OCH3 163
1529 — O CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01301
 		OC2H5 140
1530 — O CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01302
 		OC3H7 129
1531 — O CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01303
 		OCH(CH3)2 118
1532 — O CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01304
Figure USRE039607-20070501-C01305
 		133
1533 — O CH2CH2F (6-)C2H5 O CH3 CH3 290
1534 — O CH2CH2F (6-)C2H5 O CH3 C3H7 274
1535 — O CH2CH2F (6-)C2H5 O OC2H5 C2H5 118
1536 — O CH2CH2F (6-)C2H5 O CH3 N(CH3)2 170
1537 — O CH2CH2F (6-)C2H5 O CH3 SCH3 168
1538 — O CH2CH2F (6-)C2H5 O CH3 OCH3 166
1539 — O CH2CH2F (6-)C2H5 O CH3 OC2H5 140
1540 — O CH2CH2F (6-)C2H5 O CH3 OC3H7 138
1541 — O CH2CH2F (6-)C2H5 O CH3 OCH(CH3)2 136
1542 — O CH2CH2F (6-)C2H5 O CH3
Figure USRE039607-20070501-C01306
 		139
1543 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01307
 		OCH3 156
1544 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01308
 		OC2H5 138
1545 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01309
 		OC3H7 125
1546 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01310
 		OCH(CH3)2 140
1547 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01311
Figure USRE039607-20070501-C01312
 		158
1548 — O CH3 (6-)C2H5 O
Figure USRE039607-20070501-C01313
 		C4H9 149
1549 — O CH3 (6-)C2H5 O CH3 C3H7 118
1550 — O CF3 (6-)C3H7 O CH3 OCH3 94
1551 — O CF3 (6-)C3H7 O CH3 OC2H5 175
1552 — O CF3 (6-)C3H7 O CH3 OC3H7 166
1553 — O CF3 (6-)C3H7 O CH3 OCH(CH3)2 164
1554 — O CF3 (6-)C3H7 O CH3 OCH2CF3 221
1555 — O CF3 (6-)C3H7 O CH3
Figure USRE039607-20070501-C01314
 		189
1556 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01315
 		OCH3 182
1557 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01316
 		OCH2CH3 134
1558 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01317
 		OC3H7 207
1559 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01318
 		OCH(CH3)2 148
1560 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01319
 		OCH2CF3 204
1561 — O CF3 (6-)C3H7 O
Figure USRE039607-20070501-C01320
Figure USRE039607-20070501-C01321
 		186
1562 — O CH3 (6-)C2H5 O CH2CH2OCH2 163
1563 — O CH3 (6-)C2H5 O CH2CH2CH2OCH2 191
1564 — O CF3 (6-)CH3 O
Figure USRE039607-20070501-C01322
 		OCH3 197
1565 — O CH2CF2H (6-)CH3 O CH3 OCH3 231
1566 — O CH2CF2H (6-)C2H5 O CH3 OCH3 174
1567 — O CH2CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01323
 		OCH3 160
1568 — O CH2CF2H (6-)C2H5 O
Figure USRE039607-20070501-C01324
 		OCH(CH3)2 162
1569 — O CH2CF2H (6-)C2H5 O CH3 CH3 >250
1570 — O CH2CF2H (6-)CH3 O CH3 OCH2CF3 117
1571 — O CH2CF2H (6-)CH3 O CH3
Figure USRE039607-20070501-C01325
 		128
1572 — O CH2CF2H (6-)CH3 O
Figure USRE039607-20070501-C01326
Figure USRE039607-20070501-C01327
 		124
1573 — O CH2CF2H (6-)CH3 O CH3 C2H5 137
1574 — O CH2CF2H (6-)CH3 O CH3 C3H7 139
1575 — O CH2CF2H (6-)CH3 O CH3
Figure USRE039607-20070501-C01328
 		150
1576 — O CH2CF2H (6-)CH3 O CH3 CH2OCH3 114
1577 — O CH2CF2H (6-)CH3 O CH3 SCH3 155
1578 — O CH2CF2H (6-)C3H7 O CH3 CH3 290
1579 — O CH2CF2H (6-)CH3 O CH3 N(CH3)2 116
1580 — O CH2CF2H (6-)CH3 O OC2H5 C2H5 125
1581 — O CH2CF2H (6-)CH3 O
Figure USRE039607-20070501-C01329
 		CH3 137
1582 — O CH2CF2H (6-)CH3 O
Figure USRE039607-20070501-C01330
 		OC2H5 99
1583 — O CH2CF2H (6-)CH3 O
Figure USRE039607-20070501-C01331
 		OC3H7 130
1584 — O CH2CF2H (6-)CH3 O CH3 OC2H5 147
1585 — O CH2CF2H (6-)CH3 O CH3 OCH(CH3)2 151
1586 — O CH3 (6-)C2H5 O CH3 N(CH3)2 199
1587 — O CF3 (6-)C2H5 O CH3 CH═CH(CH3) 128
1588 — O CF3 (6-)C2H5 O CH3 CH2OCH3 101
1589 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01332
 		N(CH3)2 154
1590 — O CF3 (6-)C2H5 O
Figure USRE039607-20070501-C01333
 		SC2H5 143
1591 — O CF3 (6-)C2H5 O CH3 SC2H5 113
1592 — O CF3 (6-)C2H5 O OC2H5 C2H5 122
1593 — O CF3 (6-)C2H5 O OC2H5 SC2H5 133
1594 — O CF3 (6-)C2H5 O CH3 OC6H9 193
1595 — O CH2CH2F (6-)CH3 O CH3 C2H5 109
1596 — O CH2CH2F (6-)CH3 O CH3
Figure USRE039607-20070501-C01334
 		157
1597 — O CH2CH2F (6-)CH3 O CH3 CH2OCH3 106
1598 — O CH2CH2F (6-)CH3 O CH3 SCH3 135
1599 — O CH2CH2F (6-)CH3 O CH3 N(CH3)2 141
1600 — O CH2CH2F (6-)CH3 O OC2H5 C2H5 129
1601 — O CH2CH2F (6-)CH3 O
Figure USRE039607-20070501-C01335
 		CH3 169
1602 — O CH2CH2F (6-)CH3 O
Figure USRE039607-20070501-C01336
 		OC2H5 125
1603 — O CH2CH2F (6-)CH3 O
Figure USRE039607-20070501-C01337
 		OC3H7 117
1604 — O CH2CH2F (6-)CH3 O CH3
Figure USRE039607-20070501-C01338
 		145
1605 — O CH2CH2F (6-)CH3 O
Figure USRE039607-20070501-C01339
Figure USRE039607-20070501-C01340
 		118
1606 — O CH2CH2CH2F (6-)C3H7 O CH3 OCH3 127
1607 — O CH2CH2CH2F (6-)C3H7 O CH3 OCH(CH3)2 155
1608 — O CH2CH2CH2F (6-)C3H7 O
Figure USRE039607-20070501-C01341
 		OCH3 106
1609 — O CH2CH2CH2F (6-)C3H7 O
Figure USRE039607-20070501-C01342
 		OCH(CH3)2 138
1610 — O CH2CH2F (6-)C2H5 O CH3
Figure USRE039607-20070501-C01343
 		157
1611 — O CH2CH2F (6-)C2H5 O CH3 CH2OCH3 101
1612 — O CH2CH2F (6-)C2H5 O
Figure USRE039607-20070501-C01344
 		CH3 147
1613 — O CH2CH2F (6-)CH3 O CH3 C3H7 280
1614 — O CH2CH2CH2F (6-)C3H7 O CH3 CH3 302
1615 — O CH2CH2CH2F (6-)C3H7 O CH3 C3H7 261
1616 — O CH2CH2F (6-)C3H7 O CH3 C3H7 108
1617 — O CH2CH2F (6-)C3H7 O CH3 OCH3 158
1618 — O CH2CH2F (6-)C3H7 O CH3 OC2H5 152
1619 — O CH2CH2F (6-)C3H7 O CH3 OCH(CH3)2 164
1620 — O CH2CH2F (6-)C3H7 O
Figure USRE039607-20070501-C01345
 		OCH3 137
1621 — O CH2CH2F (6-)C3H7 O
Figure USRE039607-20070501-C01346
 		OC2H5 117
1622 — O CH2CH2F (6-)C3H7 O
Figure USRE039607-20070501-C01347
 		OCH(CH3)2 158
1623 — O CH2CH2F (6-)C3H7 O CH3 N(CH3)2 147
1624 — O CH2CH2F (6-)C3H7 O OC2H5 C2H5 237
1625 — O CH2CH2F (6-)C3H7 O CH3 SCH3 130
1626 — O CHF2 (6-)Br O CH3 OCH3 160
1627 — O CHF2 (6-)Br O CH3 CH3 146
1628 — O CHF2 (6-)Br O CH3 C3H7 127
1629 — O CHF2 (6-)Br O CH3 OC2H5 168
1630 — O CHF2 (6-)Br O CH3 OCH(CH3)2 126
1631 — O CHF2 (6-)Br O
Figure USRE039607-20070501-C01348
 		OCH3 145
1632 — O CHF2 (6-)Br O
Figure USRE039607-20070501-C01349
 		OC2H5 125
1633 — O CHF2 (6-)Br O
Figure USRE039607-20070501-C01350
 		OCH(CH3)2 148
1634 — O CHF2 (6-)Br O CH3 N(CH3)2 173
1635 — O CF3 (6-)F O CH3 SCH3
1636 — O CF3 (6-)F O CH3 C2H5
1637 — O CF3 (6-)F O CH3 OC2H5
The compound listed in Table 1 as Example 9 can be prepared, for example, as follows:
Figure USRE039607-20070501-C01351
(Process (b))
1.4 g (0.01 mol) of 5-ethoxy-4-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one and 2.4 g (0.01 mol) of 2-ethoxy-6-methyl-phenylsulphonyl isocyanate are stirred at 20° C. For 15 hours in 50 ml of acetonitrile. The solvent is distilled off, the residue is stirred with diethyl ether and the precipitate is filtered off with suction.
3.3 g (85% of theory) of 5-ethoxy-4-methyl-2-(2-ethoxy-6-methyl-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained of melting point 160° C.
Starting Materials of the Formula (II) or (IIa):
Figure USRE039607-20070501-C01352
64.6 g (0.26 mol) of 2-isopropoxy-6-methyl-benzenesulphochloride are stirred at 20° C. For 12 hours in 350 ml of 25% strength aqueous ammonia solution. The crystalline product is subsequently isolated by filtration with suction. 54 g (90% of theory) of 2-isopropoxy-6-methyl-benzenesulphonamide are obtained of melting point 78° C.
Figure USRE039607-20070501-C01353
A mixture of 1.9 g (10 mmol) of 2-hydroxy-6-methyl-benzenesulphonamide, 1.2 g (10 mmol) of propargyl bromide (in the form of an 80% strength solution in toluene) and 1.4 g (10 mmol) of potassium carbonate is heated under reflux for 2 hours. The mixture is then filtered, the filtrate is concentrated under a water pump vacuum, the residue is digested with petroleum ether and the crystalline product obtained from this digestion is isolated by filtration with suction.
2.1 g (93% of theory) of 6-methyl-2-propargyloxy-benzenesulphonamide are obtained of melting point 129° C.
Figure USRE039607-20070501-C01354
188 ml of a 1-molar solution of boron(II) bromide in methylene chloride are added dropwise at 20° C. with stirring to a solution of 32.3 g (0.15 mol) of 2-ethoxy-6-methylbenzenesulphonamide in 300 ml of methylene chloride, and the reaction mixture is stirred at 20° C. for 30 minutes. Then 300 ml of methanol are added dropwise at from 0° C. to 5° C. (ice cooling). After heating to 20° C., the reaction mixture is concentrated under a water pump vacuum and the residue is stirred with ethyl acetate. The solution obtained is washed with water, dried over sodium sulphate and filtered. The filtrate is concentrated under a water pump vacuum, the residue is crystallized by stirring with petroleum ether, and the crystalline product is isolated by filtration with suction.
20.3 g (72% of theory) of 2-hydroxy-6-methyl-benzenesulphonamide are obtained of melting point 126° C.
In analogy to Examples (II-1) to (II-3) and in accordance with the general description of the preparation process according to the invention, it is also possible, for example, to prepare the compounds of the formula (II) or (IIa) listed in Table 2 below,
TABLE 2
Examples of the compounds of the formula (II)
(II)
Figure USRE039607-20070501-C01355
(position-) Melting
Ex. No. A R1 R2 point (° C.)
II-4 — C2H5 (6-)CH3 104
II-5 — n-C3H7 (6-)CH3 63
II-6 — —CH2CH2Cl (6-)CH3 102
II-7 — CH3 (6-)CH3 132
II-8 — —CH2C6H9 (6-)CH3 131
II-9 — —CH2COOCH3 (6-)CH3 90
II-10 — CH3 (6-)C3H7-n 108
II-11 — C2H5 (6-)C3H7-n 80
II-12 — C2H5 (5-)CH3 131
II-13 — CH3 (6-)Cl 166
II-14 — C2H5 (6-)Cl 121
II-15 — H (6-)Cl 118
II-16 — i-C3H7 (6-)Cl 85
II-17 — —CH2CH═CH2 (6-)Cl 106
II-18 — —CH2C≡CH (6-)Cl 181
II-19 — CF3 (5-)Cl
II-20 — CHF2 (5-)CH3 127
II-21 — CHF2 (6-)CH3 89
II-22 — CH3 (5-)C(CH3)2 160
II-23 — CH3 (5-)Cl
II-24 — CHF2 (4-)CH3 153
II-25 — —CF2CHFCl (6-)CH3 85
II-26 — C2H5 (6-)CH2Cl

Starting Materials of the Formula (IV):
Figure USRE039607-20070501-C01356
21.5 g (0.1 mol) of 2-ethoxy-6-methyl-benzenesulphonamide and 10 g (0.1 mol) of n-butyl isocyanate are heated to boiling in 100 ml of chlorobenzene. At reflux temperature, phosgene is passed in for 4 hours. The clear solution is concentrated under reduced pressure and the residue is subjected to precision distillation. At a pressure of 0.8 bar and an overhead temperature of 135-140° C., 2-ethoxy-6-methyl-phenylsulphonyl isocyanate goes over and solidifies in the receiver.
7.9 g of 2-ethoxy-6-methyl-phenylsulphonyl isocyanate are obtained as a colourless product of melting point 40° C.
Starting Materials of the Formula (VI) or (VIa):
Figure USRE039607-20070501-C01357
47.8 g (0.29 mol) of 2-isopropoxy-6-methyl-aniline are dissolved in a mixture of 87 ml of 1N hydrochloric acid and 145 ml of conc. hydrochloric acid, and the solution is cooled to −5° C. At −5° C. to 0° C., a solution of 22 g (0.32 mol) of sodium nitrite in 87 ml of water is then added dropwise with stirring and the mixture is stirred at about 0° C. for a further hour. After removal of the nitrite excess with amidosulphonic acid, the diazonium salt solution obtained is added dropwise at −5° C. to 0° C. to a saturated solution of sulphur dioxide in 175 ml of 1,2-dichloro-ethane. After about 30 minutes, 1.7 g of copper(I) chloride and 1.7 g of dodecyl-trimethylammonium bromide are added, and the reaction mixture is allowed to rise to room temperature over the course of about 60 minutes, heated to about 40° C. over a further hour, and stirred at this temperature for about 12 hours. At about 20° C., 14.2 g of a 35% strength hydrogen peroxide solution are then added and the mixture is stirred for about 30 minutes. It is subsequently stirred with 300 ml of methylene chloride, and the organic phase is separated off, washed with water, dried over sodium sulphate and filtered. The solvent is carefully removed from the filtrate by distillation under a water pump vacuum.
65.9 g (90% of theory) of 2-isopropoxy-6-methyl-benzenesulphochloride are obtained as a brownish oily residue.
1H-NMR (CDCl3, TMS, δ ppm): 1.47 (d, J=6.1 Hz, 2×CH3); 2.68 (s, CH3); 4.79 (sept., J=6.1 Hz, 1H); 6.83 (d, J=7.5 Hz, 1H); 6.95 (d, J=8.4 Hz, 1H); 7.45 (pseudo t, J=8.3 Hz, 1H).
In analogy to Example (VI-1) it is also possible, for example, to prepare the compounds of the formula (VI) or (VIa) listed in Table 3 below.
TABLE 3
Examples of the compounds of the formula (VI)
(IV)
Figure USRE039607-20070501-C01358
Ex. (position-)
No. A R1 R2 Physical data
VI-2 — CH3 (6-)CH3 Fp.: 52° C.
VI-3 — C2H5 (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.55(t, J=
6.97Hz, CH3), 2.69(s,
CH3), 4.24(q, J=6.97Hz,
CH2), 6.87(d, J=7.68Hz,
1H), 6.95(d, J=8.34Hz,
1H), 7.46(pseudo t,
J=8.1Hz, 1H)
VI-4 — n-C3H7 (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.33 (t, J=
7.38Hz, CH3), 1.95(m,
CH2), 2.69(s, CH2),
4.12(t, J=6.3Hz, CH2),
6.86(d, J=7.69Hz, 1H),
6.94(d, J=8.37Hz, 1H),
7.46(pseudo t, J=7.8Hz,
1H)
VI-5 — —CH2CH3Cl (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 2.71(s, CH3),
3.94(t, J=6.1Hz, CH2),
4.41(t, J=6.1Hz, CH2),
6.96(t, J=7.1Hz, 2H),
7.5(t, J=7.8Hz, 1H)
VI-6 — —CH2CH2OC2H5 (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.23(t, J=7Hz,
CH3), 2.69(s, CH2),
3.65(q, J=7Hz, CH2),
3.91(t, J=5.16Hz, CH2),
4.30(t, J=5.16Hz, CH2),
6.89(d, J=7.7Hz, 1H),
7.0(d, J=8.3Hz, 1H),
7.47(pseudo t, J=8.1Hz,
1H)
VI-7 — C2H5 (5-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.53(t, J=7Hz,
CH3), 2.36(s, CH3),
4.25(q, J=7Hz, CH2),
7.0(d, J=8.53Hz, 1H),
7.45(d, J1=8.53Hz,
J2=2.15Hz, 1H),
7.75(d, J=2.15Hz, 1H)
VI-8 — n-C3H7 (5-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.08(t, J=
7.38Hz, CH3), 1.85(m,
CH2), 2.23(s, CH3),
3.99(t, J=6.5Hz), 6.74(d,
J=8.2Hz, 1H), 6.92(m,
1H), 7.34(d, J=1.65Hz,
1H)
VI-9 — i-C3H7 (5-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 1.45(d, J=6.06,
2xCH3), 2.35(s, CH3),
4.77(sept, J=6.06Hz,
1H), 6.99(d, J=8.57Hz,
1H), 7.43(dd, J1=
8.56Hz, 1H, J2=2.1Hz,
1H), 7.74(d, J=2.1Hz,
1H)
VI-10 — C2H5 (6-)CH2Cl (Oil)
VI-11 — —CF2CHFCl (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 2.78(s, CH3),
6.46(td, CHFCl),
7.2-7.6(Ar—H)
VI-12 — CHF2 (6-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 2.76(s, CH3),
6.61(t, CHF2), 7.27-
7.59(Ar—H)
VI-13 — CH3 (5-)C(CH3)3 Fp.: 62° C.
VI-14 — CHF2 (4-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 2.50(s, CH2),
6.68(t, CHF2), 7.05-
7.92(Ar—H)
VI-15 — CHF2 (5-)CH3 1H-NMR(CDCl3, TMS,
δ, ppm): 2.45(s, CH3),
6.64(t, CHF2), 7.35-
7.86(AR—H)
VI-16 — —CH2CH2Cl (6-)CH3
VI-17 — —CH2CH═CH2 (6-)CH3
VI-18 — —CH2C≡CH (6-)CH3
VI-19 — —CH2C6H5 (6-)CH3

Starting Materials of the Formula (X):
Figure USRE039607-20070501-C01359
Step 1: Preparation of 2-isopropoxy-6-methyl-nitrobenzene
A mixture of 153 g (1.0 mol) of 3-methyl-2-nitro-phenol, 172.5 g (1.25 mol) of potassium carbonate, 170 g (1.0 mol) of 2-iodo-propane and 400 ml of acetone is heated under reflux for 12 hours. It is subsequently concentrated under a water pump vacuum, the residue is stirred with 400 ml of methylene chloride, the mixture is filtered and the filter product is washed with methylene chloride. The solvent is removed carefully from the filtrate by distillation under a water pump vacuum.
183.4 g of 2-isopropoxy-6-methyl-nitrobenzene are obtained as a yellow oily residue.
1H-NMR (CDCl3, TMS, δ, ppm): 1.33 (d, J=6.1 Hz, 2×CH3), 2.28 (s, CH3), 4.6 (sept., J=6.1 Hz, 1H), 6.8 (d, J=7.7 Hz, 1H), 6.87 (d, J=8.4 Hz, 1H), 7.26 (pseudo t, J=8.1 Hz, 1H).
Step 2: Preparation of 2-isopropoxy-6-methyl-aniline
183.3 g (0.94 mol) of 2-isopropoxy-6-methyl-nitrobenzene are hydrogenated in 1 litre of ethyl acetate in the presence of 9.5 g of Raney nickel under a hydrogen pressure of from 40 to 60 bar for 5 hours. The mixture is then filtered and the solvent is carefully removed from the filtrate by distillation under a water pump vacuum.
139.4 g (90% of theory) of 2-isopropoxy-6-methyl-aniline are obtained as an orange-coloured oily residue. 1H-NMR (CDCl3, TMS, δ, ppm): 1.36 (d, J=6.1 Hz, 2×CH3), 2.16 (s, CH3), 3.72 (s, NH2), 4.51 (sept., J=6.1 Hz, 1H), 6.65-6.70 (m, 3H).
USE EXAMPLES
In the Use Examples, the compounds specified below are used as comparison substances
Figure USRE039607-20070501-C01360
4,5-Dimethoxy-2-(2-methoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one (known from EP 534266);
Figure USRE039607-20070501-C01361
4,5-Diethoxy-2-(2,5-dimethoxy-phenylsulphonylaminocarbonyl)-2,4-dihydro-3H-, 1,2,4-triazol-3-one (known from EP 534266).
Example A
Pre-emergence Test
Solvent: 5 parts by weight of acetone
Emulsifier: 1 part by weight of alkylaryl polyglycol ether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
Seeds of the test plants are sown in normal soil, and, after 24 hours, the soil is watered with the preparation of the active compound. It is expedient to keep constant the amount of water per unit area. The concentration of the active compound in the preparation is of no importance, only the amount of active compound applied per unit area being decisive.
After three weeks, the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control. The figures denote:
0%=no action (like untreated control)
100%=total destruction
In this test, the compounds according to Preparation Examples 1, 7-21, 23-41, 46-49, 51, 54, 55, 57, 60, 62, 65, 68, 72-74, 76, 78, 79, 88, 89, 199, 207, 209, 222 and 901 for example, exhibit a very strong action against broad-leaved weeds.
Example B
Post-emergence Test
Solvent: 5 parts by weight of acetone
Emulsifier: 1 part by weight of alkylaryl polyglycol ether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.
Test plants which have a height of 5-15 cm are sprayed with the preparation of the active compound in such a way as to apply the particular amounts of active compound desired per unit area. The concentration of the spray liquor is chosen so that the particular amounts of active compound desired are applied in 2,000 l of water/ha. After three weeks, the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control.
The figures denote:
0%=no action (like untreated control)
100%=total destruction
In this test, the compounds according to Preparation Examples 1, 7-10, 12, 13, 15, 16, 17, 25, 30, 31, 38, 40, 41, 46 and 47, for example, exhibit a very strong action against broad-leaved weeds.

Claims (6)

1. A compound of the formula (I),
Figure USRE039607-20070501-C01362
wherein
A represents a single bond,
Q represents oxygen or sulphur,
R1 represents hydrogen or formyl or represents in each case optionally cyano-, fluoro-, chloro-, bromo-, phenyl- or C1-C4-alkoxy-substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkoxycarbonyl or alkylsulphonyl having in each case up to 6 carbon atoms, or represents in each case optionally cyano-, fluoro-, chloro-, bromo- or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C3-C6-cycloalkyl-carbonyl or C3-C6-cycloalkyl-sulphonyl,
R2 represents cyano, fluoro, chloro or bromo or represents in each case optionally cyano-, fluoro-, chloro-, bromo- or C1-C4-alkoxy-substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy or alkinyloxy having in each case up to 6 carbon atoms, and
R3 represents in each case optionally substituted heterocyclyl of the formula below,
Figure USRE039607-20070501-C01363
 in which
Q1 represents oxygen or sulphur, and
R4 represents hydrogen, or amino, or represents C2-C10-alkylideneamino, or represents optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy-, C1-C4-alkyl-carbonyl- or C1-C4-alkoxy-carbonyl-substituted C1-C6 C6 alkyl, or represents in each case optionally fluoro-, chloro- and/or bromo-substituted C2-6 C2 -C 6-alkenyl or C2-6 C2 -C 6-alkinyl, or represents in each case optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkoxy, C1-C6-alkylamino or C1-C6-alkyl-carbonylamino, or represents C3-C6-alkenyloxy, or represents di-(C1-C6-alkyl)-amino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano- and/or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C3-C6-cycloalkylamino or C3-C6-cycloalkyl-C1-C4-alkyl,
R5 represents hydrogen, or represents optionally fluoro-, chloro-, bromo-, cyano-, C1-C4-alkoxy-, C1-C4-alkyl-carbonyl- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkyl, or represents in each case optionally fluoro-, chloro- and/or bromo-substituted C2-C6-alkenyl or C2-C6-alkinyl, or represents in each case optionally fluoro-, chloro-, cyano-, C1-C4-alkoxy- or C1-C4-alkoxy-carbonyl-substituted C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylamino or C1-C6-alkyl-carbonylamino, or represents C3-C6-alkenyloxy, C3-C6-alkinyloxy, C3-C6-alkenylthio, C3-C6-alkinylthio, C3-C6-alkenylamino or C3-C6-alkinylamino, or represents di-(C1-C6-alkyl)-amino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano- and/or C1-C4-alkyl-substituted C3-C6-cycloalkyl, C5-C6-cycloalkenyl, C3-C6-cycloalkyloxy, C3-C6-cycloalkylthio, C3-C6-cycloalkylamino, C3-C6-cycloalkyl-C1-C4-alkyl, C3-C6-cycloalkyl-C1-C4-alkoxy, C3-C6-cycloalkyl-C1-C4-alkylthio or C3-C6-cycloalkyl-C1-C4-alkylamino, or represents in each case optionally fluoro-, chloro-, bromo-, cyano-, nitro-, C1-C4-alkyl-, trifluoromethyl-, C1-C4-alkoxy- and/or C1-C4-alkoxy-carbonyl-substituted phenyl, phenoxy, phenyl-C1-C4-alkoxy, phenylthio, phenyl-C1-C4-alkylthio, or
R4 and R5 together represent optionally branched alkanediyl having 3 to 11 carbon atoms,
or a salt of the compound of formula (I),
and with the proviso that if R1 represents methyl then R2 does not represent 5-methoxy and if R1 represents ethyl then R2 does not represent 5-ethoxy.
2. A compound of the formula (I), according to claim 1, wherein
A represents a single bond,
Q represents oxygen or sulphur,
R1 represents methyl, ethyl, n- or i-propyl,
R2 represents chloro or methyl- , in each case in position 5 or 6- , and
R3 represents optionally substituted triazolinyl of the formula below,
Figure USRE039607-20070501-C01364
 in which
Q1 represents oxygen or sulphur, and
R4 represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, or represents propenyl or propinyl or represents methoxy, ethoxy, n- or i-propoxy, or represents cyclopropyl, and
R5 represents hydrogen, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, or represents in each case optionally fluoro and/or chloro-substituted propenyl or propinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, or represents propenyloxy or cyclopropyl,
and with the proviso that if R1 represents methyl then R2 does not represent 5-methoxy and if R1 represents ethyl then R2 does not represent 5-ethoxy.
3. A compound of the formula (I), according to claim 1, wherein
A represents a single bond,
Q represents oxygen or sulphur,
R1 represents hydrogen or formyl, or represents in each case optionally fluoro-, chloro-, bromo-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, propenyl, butenyl, propinyl, butinyl, acetyl, propionyl, butyroyl, methoxycarbonyl, ethoxycarbonyl, n- or i-propoxycarbonyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, n-, i-, s- or t-butylsulphonyl, or represents in each case optionally fluoro-, chloro- or methyl-substituted cyclopropyl, cyclopropylcarbonyl or cyclopropylsulphonyl,
R2 represents cyano, fluoro, chloro or bromo, or represents in each case optionally fluoro-, chloro-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, propenyl, butenyl, propinyl, butinyl, methoxy, ethoxy, n- or i-propoxy, n-, i- or s-butoxy, propenyloxy, butenyloxy, propinyloxy or butinyloxy and
R3 represents in each case optionally substituted heterocyclyl of the formula below,
Figure USRE039607-20070501-C01365
 in which
Q1 represents oxygen or sulphur, and
R4 represents hydrogen, or amino, or represents C3-C4-alkylideneamino, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, or represents in each case optionally fluoro-, chloro- or bromo-substituted propenyl, butenyl, propinyl or butinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, or represents propenyloxy or butenyloxy, or represents dimethylamino or diethylamino, or represents in each case optionally fluoro-, chloro-, methyl- and/or ethyl-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl,
R5 represents hydrogen, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, or represents in each case optionally fluoro-, chloro- or bromo-substituted ethenyl, propenyl, butenyl, propinyl or butinyl, or represents in each case optionally fluoro-, chloro-, cyano-, methoxy- or ethoxy-substituted methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, or represents propenyloxy, butenyloxy, propinyloxy, butinyloxy, propenylthio, propadienylthio, butenylthio, propinylthio, butinylthio, propenylamino, butenylamino, propinylamino or butinylamino, or represents dimethylamino, diethylamino or dipropylamino, or represents in each case optionally fluoro-, chloro-, methyl- and/or ethyl-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl, cyclohexenyl, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclopropylmethylthio, cyclobutylmethylthio, cyclopentylmethylthio, cyclohexylmethylthio, cyclopropylmethylamino, cyclobutylmethylamino, cyclopentylmethylamino or cyclohexylmethylamino, or represents in each case optionally fluoro-, chloro-, methyl-, trifluoromethyl-, methoxy-and/or methoxy-carbonyl substituted phenoxy, benzyloxy, phenylthio, benzylthio, or
R4 and R5 together represent optionally branched alkanediyl having 3 to 11 carbon atoms,
with the proviso that if R1 represents methyl then R2 does not represent 5-methoxy and if R1 represents ethyl then R2 does not represent 5-ethoxy.
4. The compound of formula (I) according to claim 1 wherein
A represents a single bond,
Q represents oxygen,
R1 represents 2,2-difluoro-ethyl,
R2 represents (6-)ethyl, and
R3 represents 4,5-dimethyl-2,4-dihydro-3H-1,2,4-triazol-3-on-2-yl.
5. An herbicidal composition composing an herbicidally effective amount of a compound according to claim 1 and an inert carrier.
6. A method of controlling unwanted vegetation which comprises applying to such vegetation or to a locus from which it is desired to exclude such vegetation an herbicidally effective amount of a compound according to claim 1.
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