• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1446239 Aroyl-substituted-phenyl acetic acid derivatives JANSSEN PHARMACEUTICA NV 24 Oct 1973 [24 Oct 1972 10 Sept 1973] 49580/73 Heading C2C Novel compounds of the Formula I ArCO is an aroyl-substituent the Ar function of which is a 2-thienyl, 5-alkyl-2-thienyl, 5-halo-2- thienyl, 2 - naphthyl or 3 - pyridyl group, said ArCO being in the meta- or para-position relative to the acetic acid function; R is a hydrogen atom, a halogen atom or an alkyl group, provided that when said R is a halogen atom or an alkyl group, then R 1 is a hydrogen atom and said ArCO is in the aforementioned para-position, and provided that when said R is a halogen atom, then said Ar is a 2-thienyl, 5- alkyl-2-thienyl or 5-halo-2-thienyl group; R 1 is a hydrogen atom, a halogen atom or an alkyl group, provided that, when said R 1 is a halogen atom or an alkyl group, then R is a hydrogenatom and said ArCO is in the aforementioned meta position, and provided that when said R 1 is a halogen atom, then said Ar is a 2-thienyl, 5- alkyl-2-thienyl or 5-halo-2-thienyl group; R 2 is a hydrogen atom, an allyl or alkyl group; R 3 is a hydrogen atom or an alkyl group, provided that when said R 2 is an allyl group, then said R 3 is a hydrogen atom; R 2 and R 3 may also form together an alkylene bridge, having from 2 to 5 carbon atoms; Y is a hydroxy, alkoxy, having from 1 to 8 carbon atoms; dialkylamino-alkyloxy, or an amino containing group which is an amino, anilino, halo-substituted anilino, alkylanilino, alkyloxyanilino, piperidino, 2 - hydroxyethylamino, 2 - (2 - thiazolinyl)-amino or hydroxyamino group, wherein unless otherwise stated alkyl groups contain from 1 to 5 carbon atoms, may be prepared by (1) hydrolysing a compound of the Formula IV to produce a compound of the Formula Ia (b) hydrolysing a compound of the Formula VI (c) subjecting a compound of the Formula XVIa to a Willgerodt reaction in the presence of sulphur and morpholine to form a compound of the Formula Id (d) subjecting a compound XVIa to a modified Willgerodt in the presence of rhodamine to prepare a compound of the Formula Ie (e) mono or dialkylating free acids or esters of the Formula I in which one or both of R 2 and R 3 are hydrogen to introduce alkyl groups at R 2 and R 3 (f) reacting a compound of the Formula XXI with ArH under Friedel-Crafts conditions to prepare a compound of the Formula Ij (g) hydrolysing and decarboxylating a compound of the Formula XXIII to produce a free acid of the Formula I in which R 3 is hydrogen, (h) reacting a compound of the Formula XXX with ArCOCl under Friedel-Crafts conditions to yield a free acid of the Formula I, optionally followed by esterification or amidation of compounds I in which Y is hydroxy and/or hydrolysis to form the free acid and/or forming salts thereof. Intermediates of the Formula IV are prepared by reacting ArH with a halobenzoyl chloride in a Friedel-Crafts reaction to form a halophenylarylketone which is reacted with a diethyl malonate derivative in the presence of strong base to yield the required compound. Nitriles of the Formula VI are prepared by reacting ArH with an alkyl benzoyl chloride in a Friedel-Crafts reaction to form an alkylphenylketone; which is brominated under free radical conditions to form a bromoalkylphenylarylketone which is converted to the cyanoalkylphenylarylketone and optionally when the alkyl is -CH 2 -, mono or dimethylating the methylene group. Several α - chloroalkylphenyl - 2 - thienylketones are prepared by reacting an appropriate bromo benzonitrile with an alkylmagnesium halide to form a bromophenylalkylketone which is reacted with ethylene glycol to form a 2- bromphenyl - 2 - alkyl - 1,3 - dioxolane which is reacted with magnesium and then 2-thenonitrile and the intermediate ketimine hydrolysed to form a 2-thenoylphenylalkylketone which is reduced to a α-hydroxyalkylphenyl-2-thienylketone which is chlorinated to give the required compound. Several p(α - hydroxyalkyl)phenyl- 2 - thienylketones are prepared by reacting a p-(α-hydroxyalkyl)bromobenzene with 2H-3,4-dihydropyran to form a 2 - (p - bromo - benzyloxy) - tetrahydropyran which yields the required compound on reaction with magnesium and then 2-thio phenecarbonitrile. Pharmaceutical compositions of the compounds I with the usual excipients show antiinflammatory activity and inhibit platelet aggregation when administered orally or parenterally.
    公开号:SU719490A3
    申请号:SU731973680
    申请日:1973-10-23
    公开日:1980-02-29
    发明作者:Андриан Жан Жансен Поль；Анри Поль Ван Даель Жорж；Мартин Боей Жозеф
    申请人:Жансен Фармасетика Н.В. (Фирма)；
    IPC主号:
    专利说明:

    (54) METHOD FOR OBTAINING AROMA-FERROUS-SUBSTITUTED PHENYLACETIC ACIDS
    My hydrolysis, and the resulting compound of General formula III
     snsoon
    Agso
    Sh
    where Ar, RI and R2 have the above value, i
    if necessary, they are converted into an acid halide or a complex of ethnr, which, if necessary, are reacted with an amine or alkylated, followed by isolation of the desired product.
    Example 1. To a stirred mixture of 25.25 parts of thiophene, 58.1 parts of 2-chloro-4-fluorobenzoyl chloride and 200 parts of anhydrous benzene, 78.16 parts of chlorine tin are added dropwise at room temperature. The resulting reaction mixture was poured into a mixture of ice and concentrated hydrochloric acid, stirred for several minutes and the layers were separated. The organic layer is diluted with 80 parts of toluene, washed with 200 parts of a 5% sodium hydroxide solution and 200 parts of water, dried and evaporated, the residue is distilled off, to obtain 2-chloro-4-fluorophenyl-2-thienyl ketone; t. kin. 129-130 ° C (0.5 mm Hg. Art.).
    EXAMPLE 2 To a stirred mixture of 29.5 parts of 2-methylthofen, 39.65 parts of pfluorobenzonyl chloride and 280 parts of methylene chloride, 40 parts of aluminum chloride were added portionwise, maintaining the temperature at 20 ° C (water bath), The mixture is continued for 4 hours at room temperature. The reaction mass is then poured into a mixture of ice and 50 parts of hydrochloric acid with strong unmixing. The layers are separated and the aqueous phase is washed with chloroform. The organic layer is dried and evaporated. The residue is kept in benzene and the latter is evaporated again, the residue is solidified in petroleum ether. The solid product is filtered off and the crystallization of ethanol is removed at -20 ° C to give α-fluorophenyl-5-methyl-2-thienyl ketone; m.p. 68 ° C.
    Example 3. To a stirred mixture of 29.2 parts of 2-tenoyl chloride, 22 parts of l4-fluorotoluene and 200 parts of methylene chloride, 37.4 parts of aluminum chloride were added in portions, and stirred at an boiling point for 3 hours. The reaction mixture is poured onto ice, the resulting product is extracted with chlorine methylene. The organic layer is washed with sodium bicarbonate solution and water, dried and evaporated. The residue was distilled twice, to obtain 4-fluoro-toll-2-thienol ketone; m.p. 105-106 ° C (0.2 mm Hg. Art.).
    Example 4. To a stirred mixture of 88 parts of hydrochloride chloride nkotinonla in 400 parts of fluorobenzene by the addition of 719490
    165 parts of AluMiMiMi chloride at 5-10 ° C, then the mixture is boiled for an hour, left overnight at room temperature, then poured into a mixture of ice and hydrochloric acid, the layers are separated. The aqueous phase is extracted three times with ether. The combined organic layers are discarded, and the aqueous phase is alkalinized with 40% sodium hydroxide solution. The product is extracted several times.
    chloroform. The extracts are washed twice with water, dried and evaporated. The residue is dissolved in ether. The solution is filtered, the filtrate is subjected to crystallization after diluted with petroleum ether.
    with p-fluorophenl-3-niridyl ketone; m.p. /four,.
    Example 5. 9.6 parts of a 55% sodium hydride dispersion are suspended three times in anhydrous benzene, which each time
    decant. Then 200 parts of hexamethylphosphoramide and 34.8 parts of diethyl-2-methylmalonate are added in a dropwise manner. The mixture is heated, a hot reaction occurs. After stopping the reaction, the mixture is cooled and 41.2 parts of l-fluorophenyl-2-thienyl ketone are added. The resulting mixture is heated to 100 ° C and unmixed at this temperature for 10 hours. The reaction mixture is diluted with 400 parts of benzene,
    washed twice with water, dried and evaporated. The oily precipitate is distilled off to yield diethyl-2-methyl-2-l- (2-theioyl) -phenyl malonate; t. kin. 205-210 ° С (0.4 mmHg).
    Under the conditions of this nimer they get:
    diethyl-2-methyl-2- {4- (2-tenoyl) -. "- tolyl malonate; t. kin. 186-193 ° С (0.2 mmHg); diethyl 2- 3-chloro-4- (2-tenoyl) -fenl-2 methyl malonate; t. kin. 225-235 C (0.6-0.8 mm Hg);
    diethyl - 2-methyl-2-: / g- (5-methyl-2-thenoyl) phenylmalonate; t. kin. 235-240 ° С (1 mm of mercury);
    diethyl-2-methyl- (2-naphthoyl) -phenyl-malonate;
    diethyl-2-methyl- (3-pyridylcarbonyl) -phenyl malonate; DIETHIL-2-ETHIL - (2-tenoyl) - fenl malonate; tn kn. 175-199 ° C (0.1 mmHg);
    diethyl 2-allyl-2-: l- (2-thenoyl) -phenyl malonate; m.p. 215-220 ° C (0.2 mm Hg. Art.).
    Example 6. A mixture of 30.3 parts of diethyl-2methyl-2-l- (tenoyl) phenyl-malonate and
    200 parts of a 5% sodium hydroxide solution are boiled for 6 hours. The reaction mixture is filtered and the aqueous phase is separated. The latter is sprinkled with benzene, added with concentrated hydrochloric acid solution.
    mix for 15 minutes. The product is extracted with chloroform. The extract is washed with water, dried, filtered, and evaporated. The oily residue is triturated twice with non-trapped ether. The resulting solid product is filtered off and
    twice subjected to crystallization from acetonitrile: first at -20 ° C, then at 0 ° C, receive p- (2-tenoyl) -hydratropic acid; m.p. 124.3 ° C.
    Under the conditions of this example, receive:
    H-chloro-4- (2-theioyl) -hydratropic acid; m.p. 82.5 ° C;
    p- (5-methyl-2-theioyl) -hydratropic acid; T. Il. 93.7 ° C;
    p- (2-paftoyl) - hydratropic acid; m.p. 149.7 ° C;
    (2-thioyl) - feiyl-butyl acid; m.p. 122.8 ° C;
     (2-tenopl) -feiyl-4-peitic acid; m.p. P7.1 ° C;
    3-methyl-4- (2-tepoyl) -hydratropic acid; m.p. 100.2 ° C.
    PRPMER 7. Under conditions of irimer 5, except that the equivalent of the corresponding d-fluorophenyl arylketoia and the equivalent diethyl malloiate are used for the ieropach and then repeat the conditions of example 6 with the diethylrophenylmalonates and the following results:
    p- (2-paftoyl) -cc-ethylfeiylsuccinic acid;
    p- (5-methyl-2-theioyl) -a - ethylfeiplucose acid;
    p- (3-pyridylcarboiyl) -a-ethylphenylacetic acid;
    / g- (3-pyridylcarboiyl) - a - allyl-ester and acid;
    p- (5-methyl-2-theioyl) -a - allylphenyl-acetic acid Yu;
    p- (2-iaftoyl) -allylphenylacetic acid;
    Example 8. 60 parts of diethl-2-methyl-2 - (3-iridylcarbonyl) -feiyl-maloiate are distilled, and about 20.3 parts of ethyl-3- (3-pridylcarboiyl) -hydrate are obtained: t. 235-244 ° С (3 mm of mercury.) -.
    A mixture of 10 parts of ethyl-p- {3-iridylcarboiyl) -hydrodro-irate and 50 parts of 4% sodium hydroxide solution was refluxed for 6 hours and left at room temperature. This mixture is then extracted with ether. The organic layer is discarded and the aqueous phase is acidified with a solution of hydrochloric acid. The dirty product is filtered, washed with ether and suspended in acetone. The suspension is acidified with an excess of 2-propanol, which has previously been pasted with gaseous hydrogen chloride. The salt is washed with acetone and dried; a hydrochloride of i- (3-pyridylcarbonyl) -hylratropic acid is obtained; m.p. 210 ° C.
    Example 9. A mixture of 269 parts of p-bromo-methylbenzyl alcohol and 225 parts of 2H-3,4-digitsropyraia is stirred at 0 ° C. Then 10 drops of concentrated hydrochloric acid are added and the mixture is transferred in an ice bath 24 hours. Then it is poured into 12.00 hours of asters, ether. Organized, meek.
    the phase is washed twice with sodium bicarbonate solution and twice with water, dried, filtered and evaporated.
    The residue is distilled to give 2- (7g-bromo-methyl-isyloxy) -tetrahydropran; m.p. 165-177 ° C (20 mm Hg. Art.).
    The p-bromo-a-methylbenzyl residue is measured with an equivalent amount of ./it- bromo-amethylbeisyl alcohol, obtained from 2 and (.-Bromo-o: -methylnibisyloxy) -tetrahydropiropane; kiyeni point 168-169 ° C (12 mm Hg).
    Example 10. To 400 parts of liquid ammonia, some ferric chloride and 3 parts of sodium are added, stirred for 30 minutes, after which 14.8 parts of (2-tenoyl) phenyl acetic acid are added to the medium over 30 minutes, stirred for 45 minutes . Then, 13.6 parts of methyl iodide are added dropwise to the reaction mixture, and the mixture is stirred for 2.5 hours. Then 400 parts of ether are added and stirred overnight. The ammonia is extracted and the resulting solution is acidified with dilute hydrochloric acid. The ether layer is separated and extracted with 10% sodium hydroxide solution. The extract is washed with ether, acidified and extracted with ether. The ether solution was dried over sodium sulfate and the ether evaporated under vacuum. The residue is triturated in petroleum ether, filtered and twice subjected to crystallization from acetointryl, first at -20 ° C, then 0 ° C, to obtain p- (2-thioyl) hydratotic acid.
    Example 11. A mixture of 5.2 parts of l- (2-tepoyl) -hydratropic acid, 40 parts of absolutous epochol and 0.5 parts of hydrochloric acid is boiled, then the solvent is evaporated and the residue is dissolved in ether. The ether solution was shaken with an alkali solution, separated and shaken twice with water. The ether phase is dried, filtered and evaporated to give ethyl L- (2-tenoyl) -hydratropate.
    The following esters of the formula I are obtained in the form of the corresponding and products, and the second is the process of esterification, except for using an equivalent amount of the appropriate aroyl substitution of feiyl acetic acid:
    ethyl l- (2-theionl) - a-allylphenyl acetate;
    ethyl - l- (2-theioyl) -a-ethylfeiacetate;
    ethyl - g- (2-tenoyl) -a-ethylphenylacetate;
    ethyl - l- (2-thoyl) -a-methylphenyl acetate;
    ethyl l- (2-Japhtoyl) -a-methylphenylacetate; .. -: -
    ethyl l- (5-methyl-2-tenoyl) -a-methylphenyl acetate;
    ethyl-3-chloro-4- (2-tenoyl) -a-methyl phenyl acetate ... -,,, Example 12. For a displaceable mixture of 5.2 parts of l- (2-theioyl) hydrated hydrochloric acid in parts 0.86 parts of 55i3% -HO "sodium hydride dispersion was added and stirred for 1.5 hours. Then 3.86 parts of octyl bromide and 0.01 parts of potassium iodide were added, stirring was continued for 18 hours at room temperature. The reaction mixture is poured into benzene and shaken twice with water, twice with caustic soda and soya solution twice with water. The organic phase is dried, filtered and evaporated. The residue is dissolved in ether and stirred with activated charcoal, filtered and the filtrate is evaporated again. The residue is purified by column chromatography over silica gel with chloroform. Pure fractions are collected and the solvent is evaporated, octyl - "- (2-thenoyl) hydratronate is obtained. Under these conditions, the following esters are obtained: propyl - - (2-thooyl) -a - allylphenylacetate; butyl- (g- (2-theoyl) -cc-ethylphenylacetate; octyl-l - {2-tenoyl) -a-methylphenylacetate; propyl - p- (2-naphthoyl) - a-methylphenylacetate; pentyl - 3-chloro-4- (2-theioyl) -a - methylphenylacetate. Example 13. A mixture of 1 part caustic patra in 96 parts of 2-propanol was boiled until a homogeneous mixture was obtained. 6.25 parts / g- (2-thenoyl) -hydratropic acid are then added and the mixture is stirred at reflux for 1 hour. The mixture is treated with 0.5 parts of activated charcoal and filtered through diatomaceous earth. After stirring the filtrate for 24 hours at room temperature, the product is filtered off and dried in vacuum over calcium chloride at 70 ° C, to obtain the sodium salt of - (2-thooyl) -hydratropic acid; T. Il. 187.4 ° C. 56.8 parts of methyl iodide are added to a mixture of 28.2 parts of this salt and 250 parts of hexamethylphosphoramide at room temperature, stirred at room temperature for 1 hour. The reaction mixture is poured into 1000 parts of water and the product is extracted three times with 140 parts of diisopropyl ether . The combined extracts are washed with 200 parts of water, dried, filtered and evaporated. The residue is subjected to crystallization from 35 parts of diisopropyl ether at 0 ° C, washed with cooled ether and extruded, to obtain methyl p- (2-thenoyl) -hydratropate; m.p. 62 ° C. Under similar conditions, from 1-bromopropane, the cropil- (2-tenoyl) -hydratropate is obtained as a yellow oil. Example 14. 1.3 parts of a 78% sodium hydride dispersion are suspended three times in anhydrous benzene and the latter is decanted each time. Then, 75 parts of hexamethylphosphoramide and 10.4 parts / g- (2-thooyl) -hydrate carboxylic acid are added, heated to 50 ° C and after termination of the reaction (formation of sodium salt) the mixture is cooled to room temperature. 7 parts of M- (2-chloroethyl) -Y, K-dimethylamine are added and the mixture is stirred for 18 hours at 50 ° C. The reaction mixture is cooled and extracted with 240 parts of benzene. The organic layer is washed with 100 parts of water, dilute sodium hydroxide solution and again with 100 parts of water, dried, filtered and evaporated. The residue is purified twice by column chromatography over silica gel, using chloroform first as eluent and then a mixture of chloroform and 5% methanol. After evaporation of the solvent, the residue is converted to oxalate in 2-propanol. The crude salt is filtered off and crystallized from 2-propaiol (activated charcoal) and -20 ° C to give 2- (dimethylaminoethyl) -l- (2-theioyl) -hydrate oxalate; m.p. 117.4 ° C. Repeating this example and replacing N- (2-chloroethyl) -K, K-dimethylamine with an equivalent amount of N- (3-chloropropyl) M, -dimethylamine or N- (2-chloroethyl) -N, N-diethylamine, the following compounds are obtained: oxalate 3- (dimethylaminopropyl) -p- (2-thenoyl) -hydratropate; m.p. 135-145 ° C; hydrochloride - 2 - (diethylamioethyl) -rt- (2-tenoyl) -hydropropate; m.p. 126.4 ° C. Example 15. A mixture of 4.27 parts of lithium diisoyropylamide and 50 parts of tetragus Drofuran is cooled to -78 ° C. Then 10.4 parts of methyl 2-l- (tenoylphenyl) -acetate are added and the mixture is stirred for 40 minutes. 6.25 parts of methyl iodide, dissolved in 2.15 parts of hexamethylphosphoramide, are added at -78 ° C and the mixture is then stirred for 1 hour, after which it is warmed to room temperature, poured into water. The resulting mixture is extracted with diisopropyl ether. The organic phase is washed with water, dried and evaporated. The residue is subjected to crystallization from diisopropyl ether at 0 ° C, to obtain methyl- / g- (2-tenoyl) -hydratropate. Example 16. A mixture of 5.2 parts of p- (2-tenoyl) -hydratropic acid, 4.8 parts of thioiyl chloride and 32 parts of anhydrous benzene and refluxed for 3.5 hours. The reaction mixture is evaporated, the residue is evaporated once more from benzene, L- (2-thenoyl) -hydratropoyl chloride is obtained. To a solution of 3.7 parts of p-methoxyaniline in 20 parts of dioxane, a solution of 4.2 parts of L- (2-thooyl) -hydratropoyl chloride in 25 parts of dioxane, 30 parts of dioxane is added and refluxed for 1 h. The reaction mixture is cooled to room temperature,
    filtered, the filtrate is treated with activated charcoal, filtered and evaporated in vacuo. The oily residue is triturated in ether. The solid product is filtered off, stirred twice in ether and filtered again. The product is crystallized from 2-propanol, obtained after drying in vacuum p- (2-tenoyl) hydrate-p-anisidide; m.p. 149 ° C.
    Under these conditions, the following compounds are obtained;
    L- (2-thiazoline - 2-yl) - / g- (2-thenoyl) -hydratropamid; m.p. 186.4 ° C;
    p- (2-thenoyl) -hydratropanilide; m.p. 139.8 ° C;
    p- (2-tenoyl) -hydratrop - “- toluid; T. pl. 158.3 ° C;
    4-chloro-4- (2-tenoyl) -hydrate; m.p. 169.4 ° C;
    -, ", - (2-tenoyl) -hydratroyl-piperidine; m.p. 70.3 ° C.
    Example 17. To a solution of 2.44 parts of 2-aminoethanol in 15 parts of chloroform was added a solution of 5.6 parts of L- (2-thooyl) -hydratropoyl chloride in 15 parts of chloroform at room temperature (exothermic reaction). t for 1 h. The reaction mixture is cooled and washed with a solution of 1 n. hydrochloric acid. The organic layer is separated, washed twice with water, dried, filtered and evaporated. The oily residue is triturated in petroleum ether. The solid product is filtered off and crystallized from a batch of its ether, to obtain N- (2-oxyethyl) -rt- (2-tenoyl) - hydratropamide; m.p. 87.1 ° C.
    Example 18 Gaseous ammonia was introduced into a solution of 5.8 parts of L- (2-penoyl) -hydratropoyl chloride in 80 parts of ether, and the product was expected to be an oil. The solvent is decanted and the oil is mixed twice in petroleum ether. The solvent is decanted each time. The oily residue is dissolved in 2-propanol, the solvent is evaporated. The residue is dissolved in e-liquid and after adding petroleum ether, the product is precipitated. It is filtered off and opened using silica gel column chromatography using a mixture of chloroform, methanol and acetone (8: 1: 1). The pure fractions are collected and the solvent is evaporated. The oily residue is triturated in ether. The solid product is filtered off and dried, get p- (2-tenoyl) - hydratropamide; T. P.71. 108-124 ° C.
    Example 19 To a solution of 12.6 parts of ethyl "- (2-tenoyl) -hydratropate in 35 parts of methanol, was sequentially added with cooling first a solution of 6.05 parts of hydroxylamine hydrochloride in 35 parts of methanol, and then a solution of 7.3 parts potassium hydroxide in 35 parts of methanol, stirred for 30 minutes. The mixture is filtered
    and the filtrate is stirred for 3 days at room temperature. The reaction mixture is evaporated and the residue is dissolved in water. The aqueous solution is acidified with ether. The extract is washed with water, dried, filtered and evaporated. The residue is dissolved in water, alkalized with sodium hydroxide solution, washed with ether and the aqueous phase is acidified with concentrated hydrochloric acid. The product is extracted with ether. The latter is washed with a node, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel, using a mixture of chloroform and 10% methanol as the eluent. Pure fractions are collected, the solvent is evaporated. The residue is triturated in a mixture of petroleum ether and diisopropyl ether. The solid product is filtered and subjected to crystallization from 2-propanol, get l- (2-thenoyl) -hydraterohydroxamic acid; m.p. 143.5 ° C.
    25
    权利要求:
    Claims (1)
    [1]
    1. A method for preparing aroyl substituted phenl acetic acids of the general formula
    thirty
    AgSO
    35
    where Ar is in the meta or para position to the accelerating acid group, the radical is thienyl-2-, unsubstituted or substituted by a lower alkyl group or a pyridyl-3 atom, naphthyl-2;
    RI is hydrogen, halo, or lower alkyl;
    R2 is hydrogen, allyl, or lower alkyl;
    Cs is hydrogen or lower alkyl, and if RS is lower alkyl, Ro is lower alkyl;
    Y, characterized in that the compound of the general formula
    Lgso
    60
    where Ar, RI and R2 have the above meaning, R is lower alkyl, is subjected to w, e65
    11, in this case, the hydrolysis obtained by the general formula is the compound of the general formula CH2. Where Ar, RI, and R2 have the above meaning, and if necessary, is converted to an acid halide or ester, which, if necessary, is reacted with an amine or alkylated, followed by isolation of the desired product. Sources of information taken into account during the examination 1. K. Buhler and D. Pearson. Organic syntheses, M., “World, 1973, p. 233. Priority on the signs: 10/24/72 with Ar - being in the meta position or para position to the accelerated acid
    12 5 10 15 20 group thienyl-2 radicals, unsubstituted or substituted pyridyl-3, naphthyl-2 lower alkyl group; RI is hydrogen, halo; R2 is hydrogen, allyl, or lower alkyl; Rs is hydrogen; Y is hydroxy, Ci-Sv-alkoxy. 10.09.73 with a Y-amino group, lower alkoxygroup, substituted by dialkylamino group with lower alkyl groups, anilinogroup, unsubstituted or substituted with lower alkyl radical, lower alkoxy group, halogen atom, piperidino group, hydroxyethyl amino group, 2 sets, 2-hourly, 3-hourly, oxyethyl amino group, 2-x groups, 0-halogen atom, hydroxyethyl amino group, 2-h, o-ethyl, oxyethyl amino group, 2 h, halogen atom, piperidino, oxyethyl amino group, 2; A — thienyl-2 in meta- or para-position to the acetic acid group, substituted by a halogen atom; RI is lower alkyl; R2 is lower alkyl.
    类似技术:
    公开号 | 公开日 | 专利标题
    RU2463292C2|2012-10-10|4-substituted phenoxyphenylacetic acid derivatives
    SU719490A3|1980-02-29|Method of preparing aroyl-substituted phenylacetic acids
    CA1317964C|1993-05-18|N-phenyl butenamides with pharmaceutical properties
    JP4136865B2|2008-08-20|Novel industrial synthesis of methyl diesters of 5-amino-3-carboxymethyl-4-cyano-2-thiophenecarboxylic acid and its application to the synthesis of divalent salts of ranelic acid and their hydrates
    EA007108B1|2006-06-30|New process for the industrial synthesis of tetraesters of 5-[bis|amino]-3carboxymethyl-4-cyano-2-thiophenecarboxylic acid, and application to the synthesis of vivalent salts of ranelic acid and their hydrates
    US2734904A|1956-02-14|Xcxnhxc-nh
    US4857543A|1989-08-15|Thiophene derivative and process for preparing the same
    US2443598A|1948-06-22|3-amino-4-carbethoxy-2-alkyl derivatives of thiophene
    US6657070B2|2003-12-02|Production of chirally pure α-amino acids and N-sulfonyl α-amino acids
    US3257420A|1966-06-21|Carboxylic acids alpha-substituted by at least one cyclic radical
    CN111233707B|2020-08-18|Synthesis and refining method of 4-fluorobenzoylacetonitrile
    RU1837765C|1993-08-30|Emulsifiable fungicide concentrate
    JP2001233870A|2001-08-28|3-|-5-nitro-3h-benzofuran-2-one, method for producing the same and use thereof
    US3454562A|1969-07-08|5 - carbamoylsulfamoyl - n - substitutedanthranilic acids and esters thereof
    US4098791A|1978-07-04|Process for preparing 3-|-3-amino-propionitriles
    US4927970A|1990-05-22|Substituted 3-cyclobutene-1,2-dione intermediates
    Hoek et al.1966|The synthesis of ω‐functionalized 1‐adamantylalkanes
    SU526285A3|1976-08-25|The method of obtaining derivatives of 3-and / or 2-butenoic acid
    SU722480A3|1980-03-15|Method of preparing omega-aminoalkoxycycloalkanes or their salts
    US3936443A|1976-02-03|Penicillin antibiotics
    JP3869531B2|2007-01-17|Production method of biphenyl derivatives
    WO2003050062A2|2003-06-19|PRODUCTION OF CHIRALLY PURE α-AMINO ACIDS ADN N-SULFONYL α-AMINO ACIDS
    CA2103663A1|1992-09-07|1-oxa-2,9-diphenyl-spiro|nonane derivatives as paf antagonists
    SU294329A1|METHOD FOR PRODUCING PIPERIDINE DERIVATIVES
    AT254867B|1967-06-12|Process for the preparation of new 3,5-disubstituted isoxazole derivatives
    同族专利:
    公开号 | 公开日
    DD110044A5|1974-12-05|
    AU6176573A|1975-04-24|
    ES419871A1|1976-08-01|
    YU37106B|1984-08-31|
    DE2353357A1|1974-05-09|
    JPS4993346A|1974-09-05|
    NL7314629A|1974-04-26|
    NO141651B|1980-01-07|
    NL179583C|1986-10-01|
    FI66369C|1984-10-10|
    CA1007643A|1977-03-29|
    DE2353357C2|1982-04-01|
    CH597219A5|1978-03-31|
    CS183719B2|1978-07-31|
    ATA900773A|1976-03-15|
    FR2203635A1|1974-05-17|
    IE38402B1|1978-03-01|
    HU168046B|1976-02-28|
    AT333269B|1976-11-10|
    DK154899C|1989-05-29|
    JPS5865243A|1983-04-18|
    JPS5940811B2|1984-10-03|
    IL43570A|1977-05-31|
    JPS5938237B2|1984-09-14|
    GB1446239A|1976-08-18|
    YU275973A|1982-06-18|
    IE38402L|1974-04-24|
    BG25209A3|1978-08-10|
    IL43570D0|1974-03-14|
    SE403911B|1978-09-11|
    NO141651C|1980-04-16|
    BE806389A|1974-04-23|
    FI66369B|1984-06-29|
    LU68666A1|1974-01-03|
    DK154899B|1989-01-02|
    FR2203635B1|1977-09-09|
    PH12124A|1978-11-07|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    GB1226344A|1967-07-31|1971-03-24|
    FR2113760B1|1970-11-10|1975-04-18|Roussel Uclaf|IT1036466B|1975-07-08|1979-10-30|Sigurta Farmaceutici Spa|PROCESS FOR THE PREPARATION OF DERIVATIVES OF ALPHA PHENYLPROPIONIC ACID|
    FR2345148B1|1976-03-24|1978-10-20|Lipha|
    FR2374033B1|1976-12-16|1979-04-06|Rhone Poulenc Ind|
    GB1569404A|1977-04-22|1980-06-11|Soc D Etudes Prod Chimique|-5-methyl) phenoxy acetic acid|
    GB2030131B|1978-09-12|1982-12-22|Taiyo Pharma Ind|Process for producing 2- phenyl) propionic acid|
    JPS5728709B2|1978-09-12|1982-06-18|
    JPS5728708B2|1978-09-12|1982-06-18|
    JPS5825675B2|1979-02-02|1983-05-28|Sagami Chem Res|
    JPS5823873B2|1979-02-02|1983-05-18|Sagami Chem Res|
    ES479300A1|1979-04-04|1979-07-01|Cusi Lab|An alpha-methyl-4phenyl acetic acid derivative, process for its preparation and its pharmaceutical use.|
    EP0046337A3|1980-08-20|1982-09-15|Imperial Chemical Industries Plc|Triazole compounds, a process for preparing them, their use as plant and pharmaceutical fungicides and as plant growth regulators and compositions containing them|
    CA2023954C|1989-10-17|1999-05-04|Hiroyuki Nohira|Process for the optical resolution of 2- phenylpropionic acid|
    JP6290947B2|2016-02-05|2018-03-07|テックフィールズ バイオケム カンパニー リミテッド|Positively charged water-soluble prodrugs of aryl- and heteroarylpropionic acids with very fast skin permeability|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US30007972A| true| 1972-10-24|1972-10-24|
    US39587773A| true| 1973-09-10|1973-09-10|
    [返回顶部]