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    • 专利摘要:
    Imidazole derivatives of the formula: <IMAGE> wherein R1 represents hydrogen, or an alkyl group containing from 1 to 10 carbon atoms or an alkenyl or alkynyl group containing from 2 to 10 carbon atoms, and R2, R3 and R4, which may be the same or different, each represent hydrogen, halogen or trifluoromethoxy, or a methyl, ethyl, propyl or isopropyl group optionally substituted by one or more fluorine atoms, or one of the symbols R2, R3 and R4 represents methoxy and at least one of the other symbols R2, R3 and R4 represents halogen or trifluoromethoxy or a methyl, ethyl, propyl or isopropyl group optionally substituted by one or more fluorine atoms, are new compounds useful as herbicides.
    公开号:SU805946A3
    申请号:SU782672299
    申请日:1978-10-12
    公开日:1981-02-15
    发明作者:Джилмоур Джеймс；Рой Хаттон Лесли；Вильям Парнелл Эдгар；Барбертон Деннис；Джордж Лидс Вильям
    申请人:Мэй Энд Бейкер Лимитед (Фирма)；
    IPC主号:
    专利说明:

    (54) METHOD FOR OBTAINING IMIDAZOLE DERIVATIVES
    one
    This invention relates to a process for the preparation of imidazole derivatives of the formula I
     - | N
    JANOSA Ayf
    -Y
    where R is a hydrogen atom, a linear or branched alkyl group containing 1-10 carbon atoms, a linear or branched alkenyl or alkynyl group containing 2-10 carbon atoms,
    R, .R and R may be the same or different, and each of them may be a hydrogen atom or a halogen atom or a trifluoromethoxy group or methyl, ethylpropyl or isopropyl groups, which may, if necessary, be replaced by one or several fluorine atoms, or one of R, ft and R represents a methoxy group and. at least one of R, R and R is a halogen atom, a trifluoromethoxy group or a methyl, ethyl, propyl or isopropyl group, if necessary, substituted by one
    or several fluorine atoms and at least one of the symbols R, R, R R other than hydrogen,
    possessing biological, biological activity.
    The hydrogen substitution reaction of the imino group in the imidazole ring by the action of halide alkyls is known.
    The purpose of the invention is the synthesis of new
    o compounds with biological activity.
    The goal is achieved by the fact that the compound of formula II
    .ЛкГ1 «Чд
    X is a halogen atom,
    where is r. R, R and R have
    the above values
    is reacted with an alkali metal salt of imidazole-N, H-dimethyl-4,5-dicarboxamide, with the separation of the target product.
    Example. Imidazole-N, N-dimethyl-4, 5-dicarboxamide is partially dissolved in dry dimethylformamide (10 ml) with stirring. Sodium hydride (0.24 g) is added to the mixture.
    and the temperature rises to 60 ° C,
    it is maintained by an external heat source until the solution is completed (15 min). 3,4-Dichlorobeneyl chloride (1.95 g) was added to the solution which was heated for 6 hours. The cooled reaction mixture was diluted with chloroform (50 ml) and the solution was washed with water (100 ml), dried over magnesium sulfate and evaporated to give a colorless oil, which solidifies upon rubbing with water. The solid is dried and recrystallized from a mixture of toluene (15 ml) and hexane (15 ml) to give 1- (3,4-dichlorobenzyl) -imidazole-N, m-dimethyl-4, 5-dicarb Ksamid, melting point 128-129 C, (2.0) as colorless crystals.
    Using the procedure of Example 1, but using the corresponding benzyl halide instead of 3,4-dichlorobenzyl halide, the following compounds can be obtained:
    i .- (4-bromo-3-chlorobenzyl) imidazole-N, M-dimethyl-4,5-dicarboxamide with a melting point of 127-128 (after crystallization from ethanol), obtained from 4-bromo-3-chlorobenzyl bromide;
    1- (3-bromo-4-methylbenzyl) imidazo-N, N-dimethyl-4,5-dicarboxamide with a melting point of 121.5-122 ° C (after crystallization from ethanol), obtained from 3-bromo-4-methylbenzyl chloride
    1- (3-chloro-4-methylbenzyl) imidazole-N, M-dimethyl-4,5-dicarboxamide with a melting point of 110.5-111.0 ° C (after crystallization from a mixture consisting of toluene and petroleum ether (temperature boiling C-BO) and obtained from 3-chloro-4-methylbenzyl chloride.
    1- (4-chloro-3-methylbenzyl) imidazol-N, N-dimethyl-4,5-dicarboxamide, melting point 149-15lc (after crystallization from ethanol) and obtained from 4-chloro-3-methylbenzyl chloride , f (i) -l- (.1- (3-chlorophenyl) et et al imidazole-N, .M-dimethyl-4, 5-dicarboxamide, with a melting point of 86-88 ° C (after crystallization from ethanol), and obtained from (1) (3-chlorophenyl) ethyl chloride ...,.
    (±) -1- l- (4-chlorophenyl) ethyl-imidazol-N, m-dimethyl-4, 5-dicarboxamide, with a melting point of 129-130 ° C (after crystallization from ethanol) and obtained from (±) -1- ( 4-chlorophenyl) ethyl chloride.
    (i), (3,4-dibromophenyl) ethyl lmidazol-N, N-dimethyl-4, 5-dicarbok samide, with melting point 118-120 ° C (after crystallization from cyclohexane). and obtained from (t) -l- (3,4-dibromophenyl) ethyl chloride.
    (+) (3-trifluoromethylphenyl) ethyl imidazole-N, M-dimethyl-4,5-dicarboxamide, with a boiling point of 197199 C (at 0.3 mm Hg) and obtained from (±) -1- (3 trifluoromethylphenyl) ethyl bromide;
    (±) (4-trifluoromethylphenyl), ethyl imidazole-N, N-dimethyl-4,5-dicarboxMid, with a melting point of 9597 ° C (after crystallization from cyclohexane) and obtained from (±) -1- (4-trifluoromethylphenyl) etyl bromide; d (±) -1- (3., 4-dichlorophenyl) propyl Jimidazole-H, M-dimethyl-4,5-dicarboxamide, with a melting point of 91-93 ° C (after crystallization from cyclohexane), and obtained from (±) -1- (3,4-dichlorophenyl) propyl chloride. 5 (±) (3.4 gdiulorph nyl) butyl imidazole-N, M-dimethyl-4,5-dicarboxamide, with a melting point of 134135 s (after crystallization from toluene) and obtained from (+) (3,4-di0 chlorophenyl) butyl chloride.
    The benzyl halides used as starting materials in the preparation of these compounds were obtained in the following manner:
    5 (a) in accordance with the procedure described in Example No. 4, and. intended to produce -3,4-dibromobenzyl chloride, but replacing 3,4-dibromobenzyl alcohol with the corresponding
    Q benzyl alcohol:
    3-bromo-4-methylbenzyl chloride, as a pure mobile oil, obtained from 3-bromo-4g methylbenzyl alcohol; (±) -1- (3,4-dibromophenyl) ethyl
    c chloride, with boiling point. 90-100 s (at 0.25. Mm Hg), obtained from (+) - 1- (3, 4-dlbromophenyl). ethanol (as described by Coton et al. in the Journal of Applied Chemistry, 26, p. 666.1953; (±) -1- (3,4-dichlorophenyl) propyl
     chloride, with a boiling point of 82-85 ° C
    (at 0.25 mm Hg), obtained from (±) -1- (3,4-dichlorophenyl) propanol and (±) -1- (3,4-dichlorophenyl butyl chloride), which is a light brown oil) obtained from (±) -1- (3,4-dichlorophenyl) butanol;
    c) 32.5 g of bromine (10.4 ml) was added over 15 minutes to the stirred mixture consisting of (±) -1- (30-trifluoromethylphenyl) ethanol (38 g), triphenylphosphine (56 g) and anhydrous dimethylformamide (200 ml) under a nitrogen atmosphere. The temperature of the reaction mixture is maintained at 40-50 ° C, using
    cooling with ice. Add drop by drop
    bromine, with a constant orange color, and after stirring for 15 minutes, the reaction mixture. poured into a mixture of ice water (1 l) and hexane (400 ml).
    60 The resulting mixture is filtered, the solid material is thoroughly injected with .hexane. The hexane solutions are mixed, washed with water (4 p 100 ml each), dried with sodium sulfate and distilled to give (i) -1- (3-trifluoromethylphenyl) ethyl bromide, with a boiling point of 98-105 s (at 15 mm Hg is a pure mobile oil. Using a similar procedure, but replacing (±) -1- (3-trifluoromethylphenyl) ethanol with the corresponding benelic alcohol, were obtained: (±) -1- (4-trifluoromethylphenyl) -ethyl bromide, with a boiling point, 81-84 ° C (at 13 mm Hg) and obtained from (±) -1- (4-trifluoro-mvtilphenyl) ethanol. (c) 4-bromo-3-chlorotoluene (31 , 8 g under They are heated together with bromine succinimide (27.5 g) and benzoyl peroxide (3, Ü g) in carbon tetrachloride (75 ml) while refluxing for 10 hours. The solution obtained in this way is cooled, filtered, washed with an aqueous solution of bivalent sulfate iron, dried with magnesium sulfate, filtered and evaporated to a dry product, to obtain 44 g of 4-bromo-3-chlorobenzoyl bromide, in the form of a pale-orange oil. The benzyl alcohols used as starting materials in methods (a) and (c) were obtained as follows: (1) in accordance with the procedure described in Example No. 4, intended for the preparation of 3,4-dibromobenzyl alcohol, but Replacing 3,4-dibryumbenzoic acid with 3-bromo-4-methylbenzoic acid, 3-bromo-4-methyl-benzyl alcohol was obtained in the preparation, in the form of pure orange oil of sufficient purity, suitable for subsequent reaction. (1) sodium borohydride (14.9 g) is added in portions, over 30 minutes, to a stirred solution of 3,4-dichlorobutyrophenone (65.3 g) at a temperature of 0-10 ° C. The reaction mixture thus obtained is subjected. heating by defleating for 2 hours, cooled, then sodium hydroxide solution (300 ml 2 n) is added and the reaction mixture thus obtained is heated under refluxing for 30 minutes. Methanol was removed by evaporation, and the aqueous solution was extracted with diethyl ether (5 times 200 ml). The mixed extras are washed with water (200 ml) with 2N hydrochloric acid (200 ml) and water (5 times 200 ml each time), dried with magnesium sulfate and evaporated to obtain a dry product. As a result, (±) -1- ( 3,4-dichlorophenyl) butanol, (65 g) as a light brown oil of sufficient purity that can be used for the subsequent reaction. Example 3. Using the procedure described in Example 1, but replacing 3,4-dichlserbenzyl chloride with the corresponding benzyl halide, were obtained:, 1- (3,4-diiodobenzyl) imidazole-M, N-dimethyl-4, 5-dicarboxamide, s melting point, 155-15 hp (after crystallization from ethanol) and obtained from 3,4-diiodobenzyl bromide; 1- (3,4,5-trichlorobenzyl) imidazole-N, M-dimethyl-4,5-dicarboxamide, with a melting point of 128-130 ° C (after crystallization from ethanol), and obtained from 3.4, 5-. 1: richlorobenzyl chloride. , 4-bis (trifluoromethyl) benzyl imidazole-N, M - dimethyl-4, 5-dicarboxamide, with a melting point of 142-144 ° C (after crystallization from cyclohexane) and obtained from 3,5-bis (trifluoromethyl) benzyl bromide. I ±) (4-iodophenyl) ethyl) imidazole-N, N-dimethyl-4,5-dicarboxamide, with a melting point; .132-134s (after crystallization from aqueous ethanol), and obtained from (t) -l- (4-iodophenyl) ethyl bromide; (±) (4-trifluoromethoxyphenyl) ethyl imidazbl-N, m-dimethyl-4, 5-dicarboxamide, melting point, 7879c (after crystallization from petroleum ether, with a boiling point of 60-80 ° C), and obtained from ( +) - 1- (4-trifluoromethoxyphenyl) ethyl bromide; (1) -1 l-, (3,4-dichlorophenyl) pentyl J imidazole-N, M-dimethyl-4,5-dicarboxamide, with a melting point of 142-143 ° C (after crystallization from petroleum ether, with a boiling point, 6080 ° C) and obtained from (t) -l- (3,4-dichlorophenyl) pentylorome; . (±) (3, 47dichlorophenyl) hexyl imidazole-M, H-dimethyl-4, 5-dicarboxamide, with a melting point of 114-115 ° C (after crystallization from petroleum ether, with a boiling point of 60-80 ° C) and the resulting from (±) -1- (3,4-dichlorophenyl) hexyl bromide; (+) (3,4-dichlorophenyl heptyl-imidazole-N, M - dimethyl-4, 5-dicarboxamide, melting point 97.5-99 ° C (after crystallization from petroleum ether, with a boiling point, 60-80 ° C) and obtained from (±) -1- (3,4-dichlorophenyl) heptylbromide; (±) -1-1 - (3,4-dichlorophenyl) ion :: l imidazole-N, H-dimethyl-4,5- dicarboxamide, m.p. 79-79, (after crystallization from petroleum ether, boiling point, 60-80 ° C) and obtained from (±) -1- (3,4-dichlorophenyl) ionyl chloride. Benzyl halides used as starting materials materials upon receipt of the above compounds were obtained following them way:
    (a) The procedure described in Example 4 for the preparation of 3,4-dibromobenzyl chloride, but used instead of 3,4-dibromobenzyl alcohol () (3,4-dichlorophenyl) heptanol;
    (±) -1- (3,4-dichlorophenyl) heptyl chloride, in the form of a colorless oil;
    (c) using the procedure described in example 2 (b) and intended to produce:
    (±) -1- (3-trifluoromethylphenyl) ethyl bromide, but replacing (t) -l- (3-trifluoromethylphenyl) ethanol with the corresponding alcohol;
    (±) -1- (4-trifluoromethoxyphenyl) these bromide, in the form of an orange oil, obtained from (±) l- (4-triftopermethylphenyl) -ethanol;
    (±) -, 5-bis (trifluoromethyl) phenyl ethyl bromide, with a boiling point of 97-98 ° C (at 100 mm Hg) and obtained from (t), 5-bis (triphterophenyl) phenylJethenol;
    (+) - 1- (3,4-dichlorophenyl) pentyl bromide, in the form of a small pale orange color, obtained from (+) (3,4-dichlorophenyl) pentanol;
    {j :) 3,4 - dichlorophenyl) hexyl bromide, in the form of a yellow oil, obtained from (H;) - 1- (3,4-dichlorophenyl) - hexanol;
    (f) 1 (3,4-dichlorophenyl) nonyl bromide, in the form of a yellow oil, obtained from (±) -1- (3,4-dichlorophenyl) nonanol;
    (c) According to the procedure described in Example 2 (c), for the preparation of 4-bromo-3-chlorobenzyl bromide, but instead of 4-bromo-3-chlorotoluene, 3,4-diiodotoluene is used.
    3,4-Diiodobenzyl bromide: with a melting point of 85-87 ° C.
    Some of the benzyl alcohols that were used as starting materials in the preparation of the above compounds were obtained according to the procedure described in Example 2 (c), intended for (+) - 1- {3,4-dichlorophenyl) butanol, but using instead of 3,4-dichlorobutyrophenone, the corresponding alkanophenone:
    (±) -1- (4-Iodophenyl) ethanol, in the form of an orange oil, obtained from 4-iodoacetophenone;
    (±) -1- (3,4-dichlorophenyl) pentanol, prepared from 3,4-dichloroalerophenone;
    (+) (3,4-dichlorophenyl) hexanol, in the form of a pale yellow oil, obtained from 3,4-dichlorohexaphenone
    (+) - 1- (3,4-dichlorophenyl) heptanol, in the form of a nearly colorless oil, obtained from 3,4-dichloroheptanophenone;
    (±) -1- (3,4-dichlorophenyl) nonanol, in the form of a nearly colorless oil, obtained from 3,4-dichlorononanophenone;
    (±) - 1- (4-trifluoromethoxyphenyl) ethanol was obtained as follows:
    Methyl Magnesium Yardide, obtained from magnesium (3.5 g) and Methyl iodide (20.5 in diethyl ether (50 ml), was treated with a solution of 4-trifluoromethoxybenzaldehyde (20 g), in diethyl ether (25 ml) with refluxing and re-sewing. After adding , the resulting mixture is heated at reflux for 6 hours. The resulting mixture is cooled and treated with a solution of a1 4 4Ol chloride, (35 g) in water (100 ml) at. The organic layer is separated and the aqueous layer is washed with diethyl ether (3 times 50 ml). The ether solution and the solutions obtained the result of washing is mixed, washed with water (2 times 100 ml each time), dried with sodium sulfate and evaporated to obtain a dry product. As a result, (+) (4-trifluoromethoxyphenyl) ethanol (20.3 g) is obtained as a pure colorless oil with sufficient purity for the subsequent reaction,
    The 3,4-dichloroalerophenone used in one of the above operations was obtained as follows:
    valeryl chloride (60.3 g) is added to a thoroughly mixed solution of aluminum chloride (70 g) in ortho-dichloro-benole (73.5 g). As a result, the temperature rose from 25 ° C to 47 ° C. The resulting solution was gently heated in a steam bath for 3 hours, cooled and poured into a mixture consisting of a gallon (500 g) and concentrated hydrochloric acid (100 ml) . The layers thus obtained are separated and the aqueous phase is extracted with diethyl ether (3 times 250 ml each time).
    The resulting organic phase and ether extracts are mixed, washed with water (2 times 260 ml), saturated aqueous sodium carbonate (4 times 100 ml) and water (3 times 250 ml), dried with sodium sulfate and evaporated to a dry product. The resulting solid residue is crystallized from petroleum ether with a boiling point of 60-80 ° (150 ml), resulting in 3,4-dichloro-orvalerophenone (41 g), melting point, 4041 ° C, in the form of light brown crystals.
    Using a similar technique, but using the corresponding alkanoyl chlorides instead of valeryl chloride, we obtained:
    3,4-dichlorohexanophenone, with a boiling point of 115-150 s (at 0.2 mm Hg) with a melting point less than 35 ° C, 5 and obtained from hexane-ohl chloride;
    3,4-dichloroheptafenone, with a boiling point of 140-200 ° C (at 0.3 mm Hg and obtained from heptanoyl chloride;
    3,4-Dichlorononanophenone, boiling point 155-157 ° C (at 0.25 mm Hg) and obtained from nonanoyl chloride.
    Example 4. According to the method described in example 1, but the substitutions of the above 3,4-dichlorobenzyl chloride with the corresponding benzyl halide were obtained :,
    1- (3-fluorobenzyl) imidazole-H, M-dimethyl-4, 5-dicarboxamide / melting point: 103.5-104 s (after crystallization from ethanol) and obtained from 3-fluorobenzyl chloride;
    1- (4-fluorobenzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide, with a melting point of 94-95 ° C (after crystallization from hexane) and obtained from 4-fluorobenzyl chloride; ,
    1- (3-chlorobenzyl) imidazole-M, N-dimethyl-4, 5-dicarboxamide, with a melting point of 121-121 (after crystallization from ethanol) and obtained from 3-chlorobenzyl chloride;
    1- (4-chlorobenzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide with a melting point, 13.1-132 ° C (after crystallization from ethanol) and obtained from 4-chlorobenzyl chloride; ,
    1- (3-bromobenzyl) imidazole-N, M-dimethyl-4, 5-dicarboxamide with a melting point of 114-115 ° C (after crystallization from ethanol), and obtained from 3-bromobenzyl chloride; ,
    1- (4-bromobenzyl) imidazole-N, N-dimethyl-4, 5-dicarbox.mide with a melting point of 149-150 s and obtained from 4-bromobenzyl chloride; ,
    1- (3-iodobenzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide with a melting point of 112-114 s (after crystallization from ethanol) and obtained from 3-iodobenzyl bromide ;,
    1- (4-iodobenzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide with a melting point of 150-151 ° C (after crystallization from ethanol) and obtained from 4-iodobenzyl bromide; i
    1- (3, 4-dibromobenzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide with a melting point of 118-119 ° C (after crystallization from ethanol), and obtained from 3,4-dibromobenzyl chloride; ,
    1- (3,5-dichlorobenzyl) imidazole-N, N-dimethyl-4, 5-dicarbox 1Mid, with a boiling point of 135-136 ° C (after crystallization from ethanol) and obtained from 3,5-dichlorobenzyl chloride; ,
    1- (3-methylbenzyl) imidazole-M, N-dimethyl-4, 5-dicarboxamide, with a boiling point of 84-85-s (after crystallization from ether) and obtained from 3-methylbenzyl chloride; ,
    1- (4-methyl-benzyl) imidazole-N, N-dimethyl-4, 5-dicarboxamide, with a melting point of 115-116 ° C (after crystallization from aqueous ethanol) and obtained from 4-methylbenzyl chloride;
    1- (4-ethylbenzyl) imidazole-N, yd di methyl-4,5-dicarboxamide with a melting point of 68-69 ° C (after crystallization from cyclohexane) and obtained from 4-ethylbenzyl chloride;
    1- (4-isopropylbenzyl) imidazole-N, N-dimethyl-4,5-dicarboxamide with a melting point of 54-5b (after crystallization from hexane) and obtained from 4-isopropylbenzyl chloride;
    1 p (3,4-dimethylbenzyl) imidazole-N, N-dimethyl-4 5-carboxamide, with a melting point of 168-170 seconds (after crystallization from a mixture consisting of toluene and petroleum ether, and a boiling point of 60- 80 seconds) and the resulting from 3,4-dimethylbenzyl chloride;
    1- (3-trifluoromethylbenzyl) imidazole-N, N-jediyl yl-4, 5-dicarboxamide, with a melting point of 108-110 ° C (after
    0 crystallization from a mixture consisting of hexane and ethanol) and obtained from 3-trifluoromethylbenzyl chloride;
    1- (4-trifluoromethylbenzyl) imidazole-N, N-dimethyl-4,5-dicarboxamide, with
    5 melting point 131-132 s (after crystallization from cyclohexane) and obtained from 4-trifluoromethylbenzyl chloride;
    ly (4-trifluoromethoxybenzyl) imidazole-N, 1 1-dimethyl-4, 5-dicarboxamide with a melting point of 110.5 s (after crystallization From ethanol) and obtained from 4-trifluoromethoxy benzyl chloride;
    five
    1- (3-chloro-4-methoxybenzyl) imidoaojj-N, M-dimethyl-4, 5-dicarboxamide, with a melting point of 122-12 ° C (after crystallization from a mixture consisting of toluene and cyclohexane) and semi-
    0 from 3-chloro-4-methoxybenzo chloride;
    rt) -1, (3, 4-dichlorophenyl) ethkl imidazole-i, L-dimethyl-4, 5-dicarbot: samide, with a melting point of 124-126 ° C (after crystallization from methanol)
    5 and the resulting (+) - 1- {3,4-dichloro (benyl) ethyl chloride.
    The 3,4-dibromobenzyl chloride used in one of the above processes was prepared as follows: 3,4-dibromobenzoic acid (28 g), was suspended (t), (150 ml) with stirring at 50 s. Di-Hydrobis- (2-methoxy) -aluminate
    5 Sodium to 70% by weight to volume in 52 ml of toluene) is added further over 30 minutes at 50 ° C. The mixture thus obtained is further heated in a steam bath for 1 hour, then cooled.
    权利要求:
    Claims (1)
    [1]
    Q to 20c and hydrolyzed by adding 150 ml of 6N hydrochloric acid, while cooling. The mixture thus obtained was separated and the aqueous phase was extracted with diethyl ether (100 ml). The combined organic extracts are washed with saturated sodium bicarbonate solution and water, dried with sodium sulfate, filtered and evaporated to give 3,4-dibromobenzyl alcohol, as a light red oil (19 g). The crude alcohol is dissolved in 60 ml of chloroform , and then the resulting solution is heated at reflux. Tioni chloride, in an amount of 20 ml, is added in portions, over a period of 20 minutes, to the previously obtained reaction mixture, and the resulting solution is heated under refluxing for 1 hour. The resulting reaction mixture is further subjected to evaporation to obtain a light oily residue. which is then re-diluted with chloroform (3 times 50 ml) and the mixed chloroform solutions are evaporated. The resulting residue was dissolved in ethyl ether, washed with saturated sodium bicarbonate, dried with sodium sulfate, filtered and evaporated. As a result, 3,4-dibromobenzyl chloride (20 g) was obtained, which is a pure mobile oil of satisfactory purely suitable for subsequent reactions. Using a similar procedure, but using 4-trifluoromethoxybenzoic acid instead of 3,4-dibromobenzoic acid, 4-trifluorometo-sibenzyl chloride is obtained, which is also used in one of the above processes, as a pure mobile oil. The invention method for producing azole derivatives of the general formula I (iHaNHOd-rN dHjHHOC (iH where ((is a hydrogen atom, a linear or branched alkyl group containing 1-10 carbon atoms, a linear or branched alkenyl or alkynyl group containing 2-10 carbon atoms carbon, ft. R and R can be the same or different, and each of them can be an atom: a hydrogen or a halogen atom or a trifluoromethoxy group or an methyl, ethyl, propyl or isopropyl group, which can be, if necessary replaced by one or several either fluorine atoms, or one of R, R, and R is a methoxy group, and at least one of R, R is a halogen atom, a trifluoromethoxy group, a methyl, ethyl, propyl or isopropyl group, unsubstituted or substituted one or more fluorine atoms and at least one of the symbols R, R, R and R is other than a hydrogen atom, characterized in that the compound of the formula where X is a halogen atom, R, R, R and R have the above values are reacted with the alkali metal salt of imidazole-N, M-diL | ethyl-4, 5-dicarboxamcd, with the selection of the target product. Sources of information taken into account in the examination 1. R. Elderfield. Heterocyclic compounds, M., Ed. I.L., 1961, p. 167.
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    IT7820800D0|1978-03-01|
    IE46502B1|1983-06-29|
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    法律状态:
    优先权:
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