• 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:
    A process for the preparation of compounds of general formula (I), (wherein R and R<1> stand for an aliphatic acyloxy group comprising 2-5 carbon atoms and optionally substituted by halogen or for an aromatic acyloxy group comprising 7-11 carbon atoms), which comprises reacting a compound of general formula (II), (wherein R<2> stands for hydrogen or alkyl comprising 1-4 carbon atoms) with a borone derivative of general formula (III), (wherein R<3>, R<4> and R<5> stand for an alkyl group comprising 1-4 carbon atoms and optionally substituted by halogen or for an aryl group comprising 6-10 carbon atoms). The new compounds of general formula (I) are useful pharmaceutical intermediates.
    公开号:SU1604156A3
    申请号:SU874203191
    申请日:1987-08-07
    公开日:1990-10-30
    发明作者:Хермец Иштван；Керестури Геза；Вашвари Лелле；Хорват Агнеш；Балог Мария；Ковач Габор；Месарош Золтан；Ритли Петер；Шипош Юдит；Пайор Анико
    申请人:Хиноин Дьедьсер Еш Ведьесети Термекек Дьяра Рт (Инопредприятие)；
    IPC主号:
    专利说明:

    where R (is an aliphatic acyloxy group, which can be more effectively used in the synthesis in the preparation of 1-ethyl-6-fluoro-7-substituted-A-oxo-1,4-dihydro-quinolin-3-carboxylic acids having antibacterial thermal properties.
    The purpose of the invention is to obtain new intermediates (I) in the synthesis of norfloxacin, which have advantages over known analogues.
    Example 1. A mixture of 9.3 g of boric acid and 70 g of propionic anhydride is stirred at 100 ° C for 15 minutes, after which the reaction mixture is heated to the boiling point. After half an hour, the temperature is lowered to 110 ° C and 29.8 g of ethyl - ethyl-6-fluoro-7-chloro-4-oxo-1, .4 dihydroquinoline-3-carboxylate is added. The reaction mixture, which after a few minutes turns into a thick suspension, is stirred at 110 ° C for 2 hours, then cooled to room temperature and diluted with 30 ml of water. The reaction mixture was cooled, the precipitated crystals were filtered off. In this way, 41.5 g of ethyl-6-fluoro-7-chloro-4-oxo-i, 4-dihydro-quinolin-3-carboxylic acid-boro-di (propionyloxy) anhydride is obtained, yield: 97.7 % m.p., 252 ° C (with decomposition).
    Calculated,%: C 50.70; H 4.26; N 3.29.
    C gHjgBFClNOr
     Found,%: C 50.94 H H 4.15, N 3.41.
    EXAMPLE 2 A mixture of 46.3 g of boric acid and 345 g of propionic anhydride is stirred at 100 ° C for 15 minutes, after which the reaction mixture is heated to a boil. After half an hour, the reaction temperature is lowered to PO C and 134.5 g of 1-ethyl-6-fluoro-7-chloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid is added. The reaction mixture is stirred at for 2 hours and cooled at 10 ° C. The reaction mixture is diluted with 150 ml of water and left to crystallize overnight in a refrigerator. The next morning, the precipitated crystals are filtered, washed with water and dried in vacuo. In this way, 208.6 g of boron-propionyloxy anhydride 1-ethyl-6-fluoro-7-. Is obtained; chloro-4-oxo-1,4-dihydro-quinoline-3
    with
    5 0 5 o
    five
    .
    0
    carboxylic acid, yield 98%. The product melts at (with decomposition). A mixture of the product formed with a certain amount of the compound obtained in accordance with Example 1 does not detect any decrease in the melting point.
    Froze A mixture of 9.3 g of boric acid and 54.1 g of acetic anhydride is heated at 30 minutes. The reaction mixture is cooled before and 29 are added (8 g of ethyl -1-ethyl-6-fluoro-7-chloro-4-oxo-1 4-dig hydroquinoline-3-carboxylate. The reaction mixture is stirred at 110 ° C for 2 hours, cooled to below 10 ° C and diluted with 100 ml of water. The cooled reaction mixture is left to crystallize in the refrigerator overnight. the next morning, the precipitated crystals are filtered off, washed with water and sups, thus obtaining 33.5 g of bordeaux (acetoxy) anhydride of 1-ethyl-6-fluoro-7-chloro-4-oxo-1,4-dihydro-zinoline-3-carboxylic acid, yield: 84.4%. The product decomposes at 274 C.
    Calculated,%: C 48.34, H 3.54 N 3.52i
     С Н „FC1BN0.7
    Found,% J C 48.48; H 3.43; N 3.57. I
    Example4. 2.74 g of boric acid and 22.6 g of acetic anhydride are reacted in the presence of 2 mg of zinc chloride. Boric acid is gradually added to acetic anhydride, and the reaction temperature rises to. The temperature of the reaction mixture is then slowly lowered to I and 8.79 g of ethyl 1-ethyl-6-fluoro-1,4-dihydro-7-chloro-4-oxo-3-quinoline carboxylate, which has been previously dissolved in 18 ml hot 96 wt.% / / Volume of acetic acid. The orange-red clear solution is stirred for 2 hours at 110 ° C, and then allowed to cool. The precipitated crystals are filtered and washed several times with water and once with methanol and sups. 10.8 g (92.1%) of off-white (1-ethyl-6-fluoro-7-chloro-1,4-di-gvdro-4-oxo-3-quinoline-carboxylate-0, O (-bis / acetate-0) -boron, decomposing at 273 ° C.
    i
    Calculated,%: C 48.35%; , 55%; N 3.52.
    C, ell, BC1FNO,:,
    Found,%; From 48.2%; H 3, N 3.2%.
    Example 5: 19.5 g Boron di propionyloxy anhydride derivative of 1-ethyl-6-fluoro-7-chloro-4-oxo-1,4-dihydrononoline-3-carboxylic acid and 11.9 g piperazine is reacted in 72 ml of dimethyl sulfoxide at PU C for one hour. The reaction mixture is cooled to 90 ° C.
    and add 116 ml of a 6% j (w / v) aqueous solution of sodium hydroxide. The aqueous reaction mixture is held for 1 hour at low boiling, after which it is cooled. Thus, using the desired products I, the synthesis of the final pharmacologically active derivatives of 1,4-di-hydroquinoline-3-carboxylic acids is simplified.
    权利要求:
    Claims (1)
    [1]
    Claims 1. Method for preparing anhydrides of 1 carbon to room temperature. Size-20 ethyl-6-fluoro-7-chloro-4-oxo-1,4-digvadro the pH of the solution is adjusted to 7 s, quinoline-3-carboxylic acid and boron using 96% (w / v) acetic acid acids of general formula I acid. The reaction mixture allows Rj i
    crystallize overnight in the refrigerator The next morning, the precipitated crystals are filtered, washed with water and dried under vacuum at 90-95 ° C to constant weight. Thus, 14.0 g of 1-ethyl-6-fluoro-4-oxo-1,4-dihydro-30 ro-7-piperazinoquinoline-3-carboxylic acid is obtained, yield 95.9%. The reaction product decomposes at 221. 222 ° C (from a mixture of dichloromethane and methanol).
    Calculated,%: C 60.18 H 5.68; N 13.16.
    C, eHi8FN303
    Found,%: C 60.07; H 5.74; N 13.18 „
    The starting material is obtained as follows.
    A mixture of 9.3 g of boric acid and 70 g of propionic anhydride is stirred at 100 ° C for 15 minutes, after
    Where
     aliphatic acyloxy35
    Group,
    characterized in that the compound is total II
    ; ABOUT
    COOR,
    40
    After the preparation, the temperature is lowered to 110 ° C and the mixture is increased to 29.8 g of 1-ethyl-6-fluoro-7-chloro-4-oxo-1,4-dihydroquinoline ethyl ester. 3-carboxylic acid. The reaction mixture, which turns into a thick suspension within a few minutes, is stirred at 2 hours, cooled to room temperature and diluted with 300 ml of water. The reaction mixture is cooled and the precipitated crystals are filtered. In this way, 41.5 g of boron di (propionyloxy-en
    Q
    1-ethyl-6-fluoro-7-chloro-4-hydroxy-1J 4-dihydroquinoline-3-carboxylic acid hydride derivative, yield 97.7%. The reaction product decomposes when
    Calculated,%: C 50.79; H 4.26; N 4.29.
    C gHvsAFClNOT
    Found,%: C 50.94; H 4.15; N 3.41.
    Thus, with the help of the target products I, the synthesis of the final pharmacologically active derivatives of 1,4-di-hydroquinoline-3-carboxylic acids is simplified.
    Claims 1. Method for preparing anhydrides 1 where
     aliphatic acyloxy
    Group,
    most commonly by the fact that common II
    ; ABOUT
    COOR,
    40
    45
    where Rg is hydrogen or C -C-alkyl, is reacted with a boron derivative of general formula III
    AT
    OCORs
    OCQRj
    Ocorj
    c, c group
    where R 3 is alkyl at 80-PO®C.
    2 o The method is pop. 15 distinguished by the fact that the process is carried out in the presence of a solvent, such as acetic acid.
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    同族专利:
    公开号 | 公开日
    FI873443A0|1987-08-07|
    DK412587D0|1987-08-07|
    KR940009028B1|1994-09-29|
    FI84072C|1991-10-10|
    SI8612108A8|1996-10-31|
    CA1284800C|1991-06-11|
    NO169076C|1992-05-06|
    NO873247D0|1987-08-03|
    CS908986A2|1988-03-15|
    YU210886A|1987-12-31|
    FI84072B|1991-06-28|
    HRP930558A2|1996-04-30|
    AT53212T|1990-06-15|
    CS265228B2|1989-10-13|
    HUT44566A|1988-03-28|
    JPH0742299B2|1995-05-10|
    NO169076B|1992-01-27|
    NO873247L|1987-08-03|
    KR880700803A|1988-04-12|
    US4803274A|1989-02-07|
    DD252608A5|1987-12-23|
    EP0250535B1|1990-05-30|
    JPS63501955A|1988-08-04|
    WO1987003595A1|1987-06-18|
    DE3671628D1|1990-07-05|
    DK412587A|1987-08-07|
    HU196218B|1988-10-28|
    YU45388B|1992-05-28|
    FI873443A|1987-08-07|
    EP0250535A1|1988-01-07|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    GB1195749A|1966-12-19|1970-06-24|Lubrizol Corp|Sulfur-Containing Cycloaliphatic Reaction Products and their use in Lubricant Compositions|
    JPS5534144B2|1977-05-16|1980-09-04|
    SE444566B|1977-09-20|1986-04-21|Bellon Labor Sa Roger|7-DIALKYLAMINE-6-HALOGEN-4-OXO-1,4-DIHYDROQINOLINE-3-CARBOXYLIC ACID, PROCEDURES FOR PREPARING THEREOF AND PHARMACEUTICAL PREPARATION OF THEREOF|
    JPS6011913B2|1977-12-27|1985-03-28|Koei Chemical Co|
    JPS54138582A|1978-04-19|1979-10-27|Kyorin Seiyaku Kk|Substituted quinolinecarboxylic acid|
    FR2424919B1|1978-05-03|1980-10-31|Kyorin Seiyaku Kk|SUBSTITUTED QUINOLEINECARBOXYLIC ACID AND DERIVATIVES THEREOF AND THEIR USE AS ANTIBACTERIAL AGENTS|
    JPS5533453A|1978-08-31|1980-03-08|Dainippon Pharmaceut Co Ltd|Preventive and remedy for infectious disease of fish|
    JPS5845426B2|1978-09-29|1983-10-08|Kyorin Seiyaku Kk|
    JPH0130823B2|1980-09-05|1989-06-22|Kyorin Seiyaku Kk|
    JPH0240066B2|1982-12-27|1990-09-10|Daiichi Seiyaku Co|
    JPH0833453B2|1987-05-30|1996-03-29|大阪瓦斯株式会社|Method of detecting contact position of metal pipe|HU198709B|1987-04-08|1989-11-28|Chinoin Gyogyszer Es Vegyeszet|Process for producing quinoline-carboxylic acid derivatives|
    SI8810667A8|1987-04-08|1996-04-30|Chinoin Gyogyszer Es Vegyeszet|Anhydride of quinoline carboxylic acid of boron acid and process for their production.|
    US5380845A|1987-06-24|1995-01-10|Chinoin Gyogyszer- Es Vegyeszeti Termekek Gyara Rt.|Process for the preparation of quinoline carboxylic acid derivatives|
    GR910100517A|1991-12-30|1993-08-31|Kyorin Seiyaku Kk| bis |
    ES2077490B1|1992-11-18|1996-10-16|Marga Investigacion|TRIMETILSILILIC ESTERS AND SOLVATES OF CHELATES OF QUINOLIN-3-CARBOXYL ACIDS. PREPARATION AND APPLICATION TO THE QUINOLON PROCESS.|
    ES2092963B1|1995-04-12|1997-12-16|Sint Quimica Sa|PROCEDURE FOR THE PREPARATION OF ACID 1-CICLOPROPIL-6-FLUORO-1, 4-DIHIDRO-7--5-METHYL-2,5-DIAZABICICLOHEPT-2-IL) -4 -OXO-3-QUINOLINCARBOXILICO AND ITS SALTS.|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    HU854693A|HU196218B|1985-12-09|1985-12-09|Process for preparing quinoline carboxylic acid boric acid anhydrides|
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