• 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:
    The invention relates to 1,8-benzo (c) naphthyridine derivatives, in particular the preparation of compounds of the general formula Hat R, NVR where RH, n- or iso-C1-C4-alkyl, fluorine l kil, cyclopropyl, alkoxy, alkylamino or N-formylalkyl ; pi; Nai-f. C if Rt-H, or Hal-Ri-fluorine atoms; Afk-Ci-Ch-alkyl, for the synthesis of substances with activity, such as antibacterial, which can be used in medicine. The goal is to create new intermediates of the specified purpose. The synthesis is carried out by the reaction of the corresponding amine of the f-ly R-NH2 or 3-amino-1,2,4-triazine and the quinoline derivative f-LA Q «VwW i where R N. followed by cyclization of the obtained product.
    公开号:SU1746883A3
    申请号:SU904742811
    申请日:1990-01-15
    公开日:1992-07-07
    发明作者:Антуан Мишель；Барро Мишель；Деконклуа Жан-Франсуа；Жирар Филипп；Пико Ги
    申请人:Лаборатуар Роже Беллон (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to the preparation of new 1,8-benzo derivatives (c) of naphthyridine of the general formula
    Fy y yCOOAlk
    H "VvV
    "Fc
    where R is hydrogen, linear or branched C1-C alkyl. fluoroalkyl, cyclopropyl, alkoxy, alkylamino or N-formylalkylamino. Na) -fluorine or chlorine, if RI is hydrogen, or Hal and Ri are both fluorine and Alk-alkyl, which are intermediates in the synthesis of compounds with biological activity, in particular antibacterial.
    The aim of the invention is the development, on the basis of known methods, of a method for the preparation of novel intermediates used for the synthesis of valuable biologically active substances.
    Example 1. In suspension with stirring from 19.3 g of 2- (2,7-dichloro-6-fluoro-3-quinolincarbonyl CZ-dimethylaminoethylacrylate in 250 cm of ethanol, supported
    2
    About 00 00
    with

    00
    between 10 and 15 ° C, methylamine is bubbled until 16 g of gas is absorbed. Raise the temperature to approximately 20 ° C, add 0.8 g of 1,8-diaza-5.4.0 bicyclo-7-undecene (DVI) and heat to about 75 ° C for 2 hours. After cooling to about 20 ° The product is dried, washed 2 times with 150 cm of ethanol and 2 times with 100 cm3 of ethyl ether. 15 g of 8-chloro-3-ethoxycarbonyl-7-fluoro-1-methyl-4-OXO-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a yellow solid with mp. 360-362 ° C.
    Example 2. To the suspension, with stirring, from 13.5 g of 2- (2,7-dichloro-6-fluoro-3-quinoline-carbonyl) -3-dimethylaminoethyl acrylate in 135 cm3 of ethanol is added in 5 minutes at a temperature between 10 and 15 ° C 16 g of ethylamins, increase the temperature to approximately 20 ° C, add 0.5 g of DVI and heat with stirring for 2 hours to a temperature of about 75 ° C. After cooling to a temperature of about 20 ° C, the precipitate is dried, washed with 2 times 100 cm of ethanol, 2 times 100 cm3 of ethyl ether. 10.4 g of 8-chloro-3-ethoxycarbonyl-1-ethyl-7-fluoro-4-oxo-1,4-dihydro-1,8-benzo- (c) naphthyridine are obtained in the form of a yellow solid with mp . 300-301 ° C.
    EXAMPLE 3: 8-chloro-3-ethoxycarbonyl-7-fluoro-1- (M-formyl-M-methylamino 4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine is obtained under the conditions described in example 1, but from 19.25 g of 2- {2,7-dichloro-6-fluoro-3-quinolinecarbonyl} -3-dimethylaminoethyl acrylate, 4.05 g of N-formyl-M- methyl hydrazine and 1.6 g DVI in 200 cm3 of ethanol. 16.4 g of 8-hl or-3-ethoxy-carbonyl-7-fluoro-1 - {M-for-mil-M-methylamino) -4 Oxo are obtained. -1,4-dihydro-1,8-benzo (c) naphthyridine in the form of a colorless solid with so pl. 296-298 ° C.
    PRI me R 4. A solution of 20.6 g of 2- {2,7-dichloro-6-fluoro-3-quinolinecarbonyl) -3-dimethylaminoethyl acrylate and 6 g of cyclopropylamine in 100 cm3 of trichloromethane is stirred at temperature of about 20 ° C for 24 hours. The reaction mixture is concentrated under reduced pressure (20 kPa) at 50 ° C. The residue is absorbed in. 180 cm3 of ethanol and 10 g DVI, and the resulting solution is heated to a temperature of about 78 ° C for 4 hours. After cooling to a temperature of about 20 ° C, the resulting precipitate is dried and washed with 2 times 60 cm3 of ethanol. 13.65 g of 8-chloro-1-cyclopropyl-3-ethoxycarbonyl-G-fluoro-4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a pale yellow solid with m.p. 256 ° C, which is used without further purification for the subsequent steps.
    ExampleB 8-chloro-3-ethoxycarbonyl-7-fluoro-4-oxo-1-tert-butyl-1,4-dihydro-1,8-benzo (c) naphthyridine is prepared under the conditions of example 4, but from 8.86 g of 2- {2,7-dichloro-6-fluoro-3-quinolinecarbonyl) -3-dimethyl-aminoethyl-acrylate, 4.03 g of tert-butylamine in 45 cm3 of trichloromethane, then in 4.53 g of dir and 45 cm3 of ethanol. 5 g of 8-chloro-3-ethoxycarbonyl-7-fluoro-4-oxo-1-tert-butyl-1,4-dihydro0 1,8-benzo (c) naphthyridine are obtained in the form of a yellow solid with m.p. 239 ° C.
    Example A mixture of 11.3 g of 2- {2,7-dichloro-6-fluoro-3-quinolinecarbonyl) -3-dimethyl amino ethyl acrylate and 5.65 g of 3-amino-1,2,45 triazine in 60 cm of trichloromethane is stirred 16h at a temperature of about 20 ° C. The reaction mixture is concentrated to dryness under reduced pressure (20 kPa) at a temperature of about 30 ° C. 60 absorbs residue
    0 cm of ethanol and 5.6 g DVI and heated to a temperature of about 75 ° C for 20 hours. After cooling to 20 ° C, the insoluble part is dried and washed with 2 times 40 cm of ethanol. 6.1 g of 8-chloro-3-ethoxycar5 bonyl-7-fluoro-4-oxo-1,4-dihydro-1,8-benzo- (c) naphthyridine are obtained in the form of a brown solid decomposing at 378-380 ° C, which can be used without any other purification for the subsequent stages.
    Example. To a suspension of 1.9 g of 2-fluoro-ethylamine hydrochloride in 25 cm3 of trichloromethane, 2.7 cm3 of triethylamine are added. At the temperature of about 20 ° C, 3.5 g of 2- (2,7-dichloro-6-fluoro-3-quinolinecarbonyl) -3-dimethylamino-ethyl acrylate are added to the resulting solution. After 16 hours of stirring at this temperature, the solution is concentrated to dryness under reduced pressure (20
    0 kPa) at a temperature of about 50 ° C. The residue is taken up in 20 cm of ethanol and 3 cm3 of triethylamine and heated at 75 ° C with stirring for 2 hours. After cooling to approximately 20 ° C, insoluble
    Part 5 is dried, washed with 2 times 10 cm of ethanol, 2 times with 10 cm3 of isopropyl ether. 1.9 g of 8-chloro-3-ethoxy-carbonyl-7-fluoro-1- (2-fluoroethyl) -4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained.
    0 form a yellow solid with so pl. 268 ° C, which can be used without other purification for the subsequent steps.
    PRI me R 8. A suspension with stirring of 5.27 g of 2- (2-chloro-b, 7-difluoro-3-hino5 lincarbonyl) -3-cyclopropylamino-ethyl amylate in 2.22 g of 1.8-diaza- (5 , 4,0) bicyclo-7-undecene (DWI) and 120 cm of ethanol are heated at a temperature of about 75 ° C for 35 minutes. After cooling to a temperature of about 20 ° C, the reaction mixture is absorbed
    100 cm of water, extracted once with 100 cm3 and 2 times with 50 cm3 of trichloromethane. The combined organic extracts are washed 3 times with 50 cm of water, dried on magnesium sulphate, filtered and concentrated under reduced pressure (20 kPa) at a temperature of about 20 ° C. The obtained dry extract absorbs 30 cm3 of dried isopropyl ether and recrystallizes from a mixture of 75 cm3 of ethanol and 75 cm3 of dimethylformamide. 3.57 g of 1-cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a yellow solid with mp. 229-230 ° C.
    PRI me R 9. A suspension of 1.7 g of methoxyamine hydrochloride in 40 cm3 of trichloromethane is added to 2.13 gtriethylamine. After 15 minutes of stirring at a temperature of about 20 ° C, 3.39 g of 2- {2-chloro-6,7-difluoro-3-quinoline-carbonyl) -3-dimethylamino-ethyl acrylate is added to the resulting solution and stirred for 4 hours. h 30 min at a temperature of about 20 ° C. The reaction mixture is concentrated to dryness under reduced pressure (20 kPa) at a temperature of about 50 ° C. The residue is absorbed by 70 cm3 of ethanol, 3.6 g of triethylamine and heated to a temperature of about 75 ° C for 30 minutes. After cooling to a temperature of about 20 ° C, the obtained precipitate is dried and washed 3 times with 30 cm3 of ethanol. 2.67 g of 3-ethoxycarbonyl-7,8-difluoro-1-methoxy-4-oxo-1, 4-dihydro-1.8-benzo (c) naphthyridine are obtained in the form of a pale yellow solid with m.p. 266-268 ° C.
    PRI me R 10. In suspension with stirring from 22.3 g of 2- (2-chloro-6.7-difluoro-3-quinoline-carbonyl U-dimethylaminoethyl acrylate in 480 cm of ethanol, maintained at a temperature of about 0 ° C, in 10 minutes at a temperature between 0 and 5 ° C, a solution of 11.3 g at a temperature of about 0 ° C of methylamine in 50 cm3 of ethanol is added, the mixture is stirred for 1 hour between 0 and 5 ° C, the temperature is raised to approximately 25 ° C and mix for another 16 hours at the same temperature. The insoluble part is dried, washed 3 times with 100 cm of ethanol and 2 times with 100 cm 3 of ethyl ether. After 1 recrystallization from 250 cm 3 of di Ethyl formamide gives 16 g of 3-ethoxycarbonyl-7,8-difluoro-1-methyl-4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine in the form of a yellow solid with mp 323-324 ° s
    Example 11. To a suspension of 20 g of 2- (2-chloro-6,7-difluoro-3-quinolinecarbonyl) -3-dimethylamino-ethyl acrylate in 200 cm3 of ethanol at approximately 2 ° C is added in 10 minutes at a temperature between 2 and 5 ° C at
    stirring the solution at approximately 2 ° C from 14.6 g of ethylamine in 200 cm3 of ethanol, stir for another 40 minutes between 2 and 5 ° C, then raise the temperature to approximately 20 ° C in 2 hours. After 24 hours at a temperature of about 20 ° C the insoluble part is dried, washed with 2 times 30 cm of ethanol and 2 times with 50 cm3 of isopropyl ether. 16.35 g of 3-ethoxycarbonyl-1-ethyl-7,8-difluoro-4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a beige solid with .pl. 290 ° C.
    PRI me R 12. In suspension with stirring from 19.3 g of 2- {2-chloro-6,7,8-trifluoro-3-quinolinecarbonyl) -3-dimethylaminoethylacrylate in 150 cm3 of ethanol, maintained at a temperature of about 5 ° C, add for 10 minutes between 5 and 10 ° C. the solution at-temperature is approximately 5 ° C from 10 g of methylamine in 50 cm3 of ethanol, stirred for 1 hour between 5 and 10 ° C and increase the temperature to approximately 20 ° C . The resulting solution is combined with 7.7 g DVI and heated to approximately 30 ° C for 1 hour. After cooling to a temperature of about 20 ° C, the product is dried, washed 2 times with 100 cm of ethanol and 2 times with 100 cm 3 of isopropyl ether. 13.4 g of 3-ethoxycarbonyl-7.8,9-trifluoro-1-methyl-4-oxo-1.4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a yellow solid with m.p. 320 ° C. it is used without further purification for the subsequent steps.
    Example13. Under stirring from 7.1 g of 2- (2-chloro-6,7,8-trifluoro-3-quinolinecarbonyl) -3-dimethylaminoethyl acrylate in 100 cm3 of ethanol, maintained at a temperature of about 5 ° C, added to the suspension over 10 min between 5 and 10 ° C 4.5 g of ethylamine, stirred for 1 h between 5 and 10 ° C and increase the temperature to approximately 20 ° C. To the resulting solution, 4 g of 1,8-diaz-OZDOE-bicyclo-undecene (DWI) is added and heated to a temperature of about 75 ° C for 1 h 30 min. After cooling to a temperature of about 20 ° C, the product is dried, washed with 2 times 30 cm3 of ethanol and 2 times 50 cm3 of isopropyl ether. 4 g of 3-ethoxycarbonyl-1-ethyl-7.8,9-trifluoro-4-oxo-1,4-dihydro-1,8-benzo (c) n-aftiridine are obtained in the form of a cream solid with mp, 284 ° C, which is used without further purification for the subsequent steps.
    Example 14. In a solution with stirring, from 11.7 g of 2- (2-chloro-6,7,8-trifluoro-3-quinoline-carbonyl) -3-dimethylaminoethyl acrylate in 150 cm3 of trichloromethane at a temperature of about 20 ° C at the same temperature for 5 minutes, 9.5 g of t-butylamine.
    After 4 hours of stirring at about 20 ° C, the solution is concentrated to dryness under reduced pressure (20 kPa) at a temperature of about 50 ° C. The residue obtained absorbs 100 cm3 of ethanol. To the resulting solution, add 5 g of DVI and heat to about 75 ° C for 3 hours. After cooling to about 20 ° C, the resulting precipitate is dried, washed with 2 times 50 cm3 of ethanol and 2 times 50 cm3 of isopropyl ether. 9.5 g of 3-ethoxycarbonyl-7,8,9-trifluoro-4-oxo-1-t-butyl-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a colorless solid with m.p. 229 ° C, which can be used without other purification for the subsequent steps.
    Example 15. To a solution of 7 g of 2- (2-chloro-6,7,8-trifluoro-3-quinolinecarbonyl) -3-dimethylaminoethyl acrylate in 100 cm 3 of trichloromethane, maintained at a temperature of about 20 ° C, in 5 minutes 4.12 g cyclopropylamine and stirred for another 4 hours at the same temperature. The reaction mixture is concentrated under reduced pressure (20 kPa) at approximately 50 ° C. The oily residue obtained absorbs 100 cm3 of ethanol and 3 g of DWI. The mixture is heated to 80 ° C and maintained under stirring at this temperature for 1 hour and 30 minutes. After cooling to approximately 20 ° C, the insoluble part is dried, washed with 2 times 30 cm3 of ethanol and 2 times with 30 cm3 of isopropyl ether. 4.5 g of 1-cyclopropyl-3-ethoxycarbonyl-7,8,9-trifluoro-4-oxo-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a colorless solid with mp. 260 ° C.
    Example 6. To a suspension of 5.1 g of methyl hydroxylamine hydrochloride in 120 cm3 of trichloromethane was added 8.7 cm of triethylamine. 7.8 g of 2- {2-chloro-6,7,8-trifluor-3-quinolinecarbonyl) -3-dimethylamino-t-acylate are added to the resulting solution at approximately 20 ° C. After 2 hours of stirring at this temperature, the solution is concentrated to dryness under reduced pressure (20 kPa) at approximately 50 ° C. The residue obtained absorbs 150 cm3 of ethanol and 10 cm3
    triethylamine and heated with stirring for 30 minutes. After cooling to approximately 20 ° C, the insoluble part is dried, washed 3 times 50 cm
    ethanol and 2 times 50 cm3 of simple isopropyl ether. After 1 recrystallization from 120 cm3 of dimethylformamide, 9 g of 3-ethoxycarbonyl-6,7,8-trifluoro-1-methoxy-4-OXO-1,4-dihydro-1,8-benzo (c) naphthyridine are obtained in the form of a yellow solid. from m.p. 298-300 ° C.
    权利要求:
    Claims (1)
    [1]
    The invention The method of obtaining derivatives of 1,8-biszo (c) naphthyridine of the general formula
    ABOUT
    СООА1К
    (I)
    20
    R,
    where R is hydrogen, linear or branched Ci-Gi-alkyl, fluoroalkyl, cyclopropyl, alkoxy, alkylamino or M-formylalkylamino, Hal is fluorine or chlorine, if RI is hydrogen, or Hal and RI are both fluorine, Alk - C1-C4-alkyl, characterized in that 3-amino-1.2,4-triazine, in the case when in compound IR is hydrogen, or an amine of the general formula
    R-NHa,
    where R has the indicated meanings, in addition to hydrogen, is reacted with a quinoline derivative of the general formula
    about
    YYYr СООА1 Hat TN-a
    where Ri, Alk and Hal are as indicated, followed by cyclization of the resulting product.
    The priority is following signs: 01/16/89 when R is hydrogen, alkyl, cyclopropyl, alkylamino or M-formylalkylamino, Ri is hydrogen. Na - chlorine.
    07.28.89 when R is hydrogen, alkyl, cyclopropyl, alkyloxy, alkylamino or M-formylalkylamino, RI is hydrogen, Na is fluorine.
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    同族专利:
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    KR0145181B1|1998-07-15|
    PT92877B|1995-11-30|
    US4970213A|1990-11-13|
    AT98961T|1994-01-15|
    HU900140D0|1990-03-28|
    JPH02247177A|1990-10-02|
    JP2865761B2|1999-03-08|
    HUT53365A|1990-10-28|
    PT92877A|1990-07-31|
    EP0379414B1|1993-12-22|
    KR900011769A|1990-08-02|
    NZ232092A|1992-05-26|
    PT92878B|1995-11-30|
    IE900159L|1990-07-16|
    ES2062427T3|1994-12-16|
    IL93063D0|1990-11-05|
    AU623473B2|1992-05-14|
    IE63065B1|1995-03-22|
    DE69005319D1|1994-02-03|
    IL93063A|1994-05-30|
    HU205114B|1992-03-30|
    EP0379414A1|1990-07-25|
    PT92878A|1990-07-31|
    AU4794690A|1990-07-19|
    CA2007761C|2001-03-20|
    DE69005319T2|1994-05-05|
    CA2007761A1|1990-07-16|
    DK0379414T3|1994-02-14|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US4229456A|1977-07-18|1980-10-21|Merck & Co., Inc.|Substituted naphthyridinones and processes for their preparations|
    US4133885A|1977-07-18|1979-01-09|Merck & Co., Inc.|Substituted naphthyridinones|
    DE3302126A1|1983-01-22|1984-07-26|Boehringer Ingelheim KG, 6507 Ingelheim|Amino acid derivatives, process for their preparation and use|
    CS274601B2|1983-07-27|1991-09-15|Dainippon Pharmaceutical Co|Method of 1,8-naphthyridine derivative production|
    NZ232091A|1989-01-16|1990-12-21|Bellon Labor Sa Roger|7-fluoro-8--4-oxo-1,4-dihydro-benzonaphthyridine-3-carboxylic acid derivatives, preparation and pharmaceutical compositions thereof|
    AU623475B2|1989-01-16|1992-05-14|Laboratoire Roger Bellon|New benzonaphthyridine derivatives, their preparation and compositions containing them|NZ232091A|1989-01-16|1990-12-21|Bellon Labor Sa Roger|7-fluoro-8--4-oxo-1,4-dihydro-benzonaphthyridine-3-carboxylic acid derivatives, preparation and pharmaceutical compositions thereof|
    AU623475B2|1989-01-16|1992-05-14|Laboratoire Roger Bellon|New benzonaphthyridine derivatives, their preparation and compositions containing them|
    FR2682384B1|1991-10-10|1995-04-07|Bellon Laboratoires|PROCESS FOR THE PREPARATION OF BENZONAPHTYRIDINES.|
    FR2682378B1|1991-10-10|1995-04-07|Bellon Laboratoires|NOVEL DERIVATIVES OF FLUOROQUINOLEINE ACID CARBOXYLIC-3 AND THEIR PREPARATION.|
    FR2703681B1|1993-04-08|1995-05-12|Bellon Labor Sa Roger|PROCESS FOR PREPARING FLUORO-6-HALOGENO-2 QUINOLEINE|
    法律状态:
    2007-12-20| REG| Reference to a code of a succession state|Ref country code: RU Ref legal event code: MM4A Effective date: 20060116 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR898900430A|FR2641783B1|1989-01-16|1989-01-16|NOVEL BENZONAPHTYRIDINE-1,8 DERIVATIVES, THEIR PREPARATION AND THE COMPOSITIONS CONTAINING THEM|
    FR8910220A|FR2650277B1|1989-07-28|1989-07-28|NOVEL BENZONAPHTYRIDINE-1,8 DERIVATIVES AND THEIR PREPARATION|
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