• 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:
    New bicyclic compounds of the general formula (I), <IMAGE> (I) wherein R1 and R2 each represent a C1-6 alkyl group, and R3 is an etherified hydroxy group of the formula -CR4, wherein R4 is benzyl group, benzhydryl group or a phenyl group bearing optionally a phenyl or a trihalomethyl substituent or one or more halogen substituent(s), or R3 is an esterified hydroxy group of the formula -OCO-R5, which represents a phenyl-(C1-5 alkyl)-carbonyloxy group, a cinnamoyloxy group having optionally a halogen or one or more C1-4 alkoxy substituent(s), a benzoyloxy group having optionally a C1-4 alkyl, phenyl or trihalomethyl substituent or one or more C1-4 alkoxy substituent(s), one or more halo substituent(s) and/or nitro substituent, a benzyloyloxy group, a xanthene-9-carbonyloxy group, an optionally substituted naphthoyloxy group, or an acyloxy group derived from a five- or six-membered heterocyclic carboxylic acid bearing optionally a halo substituent on the ring, are prepared by etherifying or esterifying a bicyclic compound of the general formula (II), <IMAGE> (II) wherein R1 and R2 are as defined above. The new compounds according to the invention possess anti-arrhythmic effects and can be applied to advantage in the therapy of cardiac rhythm disorders.
    公开号:SU1222197A3
    申请号:SU823465423
    申请日:1982-07-19
    公开日:1986-03-30
    发明作者:Надор Карой；Крайшш Габор；Шинко Каталин；Пароцаи Маргит；Карпати Эгон；Спорни Ласло
    申请人:Рихтер Гедеон Ведьесети Дьяр Рт (Инопредприятие)；
    IPC主号:
    专利说明:

    12221
    This invention relates to a process for the preparation of new bicyclic compounds of the formula I
    one /
    Nt sh
    1 n
     about
    , -R
    V
    20
    . 25
    thirty
    de R and R is a methyl or ethyl group R is an esterified hydroxyl group of the formula OR, where R is phenyl unsubstituted or substituted by halogen, benzhydryl,
    or stereoisomers of these compounds, or their pharmaceutically acceptable salts with acids, which have an antiarrhythmic effect.
    The aim of the invention is to develop a method for the preparation of new bispikononan ring-substituted bicyclonane ring derivatives with a higher level of antiarrhythmic effect compared to structural analogs — bispidin derivatives, which are not substituted in position 9.
    Example 1. To a solution of 5.0 g of 3,7-dimethyl-3, 7-diazabicyclo (3.3. I) nonan-9-ol in 50 ml of dry dimethylformamide in a nitrogen atmosphere was added 1.08 g of sodium hydride. When the spontaneous evolution of hydrogen ceases, the reaction mixture is moved at 30 minutes, after which 4.8 g of fluorobenzene is added in one portion. The reaction mixture is then held at 60-100 ° C for 30 minutes until the reaction is complete. When the reaction was stopped, the reaction mixture was diluted with 10 ml of methanol to decompose excess sodium hydride, after which the mixture was acidified with 7 ml of hydrochloric acid and evaporated in vacuo. The residue is dissolved in 50 ml of water. and the resulting solution is extracted twice with 50 ml of diethyl ether to remove a non-basic substance. Then, potassium carbonate is added to the aqueous phase until the oily residue is separated, which is extracted in a separator thief with diethyl ether (3 times 50 ml). The ether extracts are combined, dried over anhydrous magnesium sulphate, filtered and the filtrate is evaporated to dryness, after which the resulting free base is converted into
    40
    50
    55
    20
    25
    thirty

     . ,
    40
    50
    55
    97
    fumarate by treatment with an equivalent amount of fumaric acid. Said salt was obtained in 71.9% yield based on the free base.
    The fumarate 3,7-dimethyl-9-phenoxy-3,7-diazabicyclo (3.3.1) nonane obtained in this way has a melting point of 196-197 ° C (after recrystallization from a mixture of ethanol and diethyl ether). The corresponding free base is a colorless oily substance with m, kip. 121-122 ° C at a residual pressure of 10-Pa; refractive index, 5472.
    The 3,7-dimethyl-3,7-diazabicyclo (3.3.1) nonan-9-ol used as the starting material was obtained from the known compound 3,7-dimethyl-3, 7-diazabicyclo (3.3.1) nonane - 9-one by catalytic hydrogenation. 3.7-Dimethyl-3, 7-diazabicyclo (3.3.I) nonan-9-ol is a crystalline substance with mp 131-131 ° C (after recrystallization from hexane).
    Example 2. 1 mol-eq of 3,7-dimethyl-3, 7-diazabicyclo (3.3.1) nonan-9-ol is reacted with 1.5 mol-eq. 4-chlorophenyl fluoride, as described in Example 1, to produce 3,7-dimethyl-9- (4-chlorophenoxy) -3,7-diazabicyclo (3.3.1) nonane fumarate; the yield of the target product is 51% of theory; T.PL.211 C (after recrystallization from a mixture of methanol and diisopropyl ether).
    Example The south of 3,7-dimethyl-3,7-diazabicyclo (3.3.1) nonan-9-ol is reacted with 24.7 g of benzhydryl bromide using the procedure described in Example 1. The product obtained as a free base is converted into fumarate, the salt is dissolved in methanol and precipitated with methyl ethyl ketone. The target fumarate 3,7-dimethyl-9-benzhydyloxy-3,7-diazabicyclo (3.3.1) nonane is obtained in a yield of 50%; m.p. D
    200-201 s.
    ft Example4. South 3-meter-7-7
     ethyl 3,7-diazabicyclo (3.3.1) nonan-9-ol is dissolved in 50 ml of dry dimethylformamide and reacted with 8.93 g of fluorobenzene as described in Example 1. The product is purified by vacuum distillation. The target Z-me-a of til-7-ethyl-9o-phenoxy-3,7-diazabicyclo (3.3.1) nonane is obtained with a yield of 69.3%; bp free base
    .3
    132-134 ° C at a residual pressure of 18 Pa; the refractive index is 1.5412.
    The dihydrochloride obtained from this base has a melting point of 230-231 ° C (after recrystallization from a mixture of isoprpanol and methyl ethyl ketone). 3-Metsch-7-ethyl-3,7-diazabicyclo (3.3.1) nonan-9-ol, used as the starting material in the described reaction, is prepared in accordance with the following procedure.
    3-Methyl-7-ethyl-3, 7-diaza6-cyclo (3.3.1) noNan-9-one is obtained from 1-methyl-4-piperidone, paraformaldehyde and ethylamine, b.p. 96-9T with (3 Pa) n5 -U4971.
    18.2 g of the obtained 3-methyl-7-these 3,7-diazabuikylo (3.3.1) nonan-9-one is dissolved in 150 ml of ethanol and the solution is hydrogenated for about 4 hours at a pressure of 4 MPa in the presence of 1 g of platinum oxide (IV) used as a catalyst. The reaction mixture contains, upon completion of the reaction, two possible isomers in a 50:50 ratio. The isomer, in the structure of which the hydroxyl group in position 9 is on the side of the K-ethyl group, is called the oL-isomer, while the isomer in which the hydroxyl group in position 9 is on one side with the K-methyl nyy group, is called the isomer.
    This mixture of isomers is treated with an alcoholic solution of hydrogen chloride in isopropanol. The oL-isomer, which is added as a dihydrochloride, is separated from the mother liquor and twice recrystallized from isopropanol. As a result, a hydrochloric salt weighing 7.7 g (60% yield) is obtained, mp. 250 C (with decomposition).
    According to the analysis by thin layer chromatography on plates with a thin layer of Kieselgel 60 adsorbent and when used as mobile phases (eluents) solvent mixtures consisting of ethanol and 25% aqueous ammonia in a ratio of from 9: 1 to 7: 3 This compound is characterized by homogeneity (one spot on the chromatograms obtained in different solvent systems).
    Uterine solutions resulting from the crystallization of the ot-isomer
    22197
    combined and evaporated, after which the resulting 18 g salt was dissolved in 50 ml of water. The solution is saturated with potassium carbonate and in excess of 5 EC, the free base is extracted with chloroform (5 times 60 ml). The chloroform extracts are combined, dried over anhydrous1-1 magnesium sulfate, filtered from the drying agent and the filtrate
    10 evaporated in vacuo to dryness. Crystallization of the residue from petroleum ether (bp) results in the production of stereochemically pure 3-methyl-7-ethyl-3,7-diazabicyclo (3.3.1) but 15 nan-9p-ol, which represents
    is a colorless crystalline substance with so pl. 98-99 C. The yield of this product after four stages of recrystallization is 2.7 g (30%). Uniformity of the treatment thus obtained. isomer was proved by thin layer chromatography; the spatial position of the 9 p -hydroxyl group is confirmed by the data of 1Н NMR-spectroscopic 25 FDI.
    Example 5. 3-Methyl-7-etsh1-3,7-diazabicyclo (3.3.1) nonan-9L-ol, prepared as described in Example 4, is converted into the following 9c (.-Aryloxypropan 30 derivatives, following the procedure described in example 1:.
    a) Z-methyl-7-ethnl- .. 9o (- (4-chlorophenoxy) -3,7-diazabicyclo dihydrochloride (3.3. Ononan; yield 51.5%; mp 139-141 C (after recrystallization from mixtures of isopropanol and diethyl ether);
    b) 3-Metsh1-7-etsh1-9o / - (2-chlorophenoxy) -3,7-diazabicyc dihydrochloride Q lo (3.3. Ononan; yield 40%; mp, 241 242 C (after recrystallization from ethanol, acetone and diethyl ether).
    The biological effect of the new compounds of formula I was studied as follows.
    The rats were first injected with 1 mg / kg of aconitine intravenously in order to cause a heart rhythm disorder, after which they were administered intravenously. but compound T and determined the dose required to restore the heart rate in 50% of the animals (, mg / kg).
    50
    55 The acute toxicity of these compounds was studied in experiments on mice with intravenous administration and the results of these experiments were used to determine s that caused 50% mortality of experimental animals (mg / kg). Lidocaine was used as a reference substance in both tests.
    The results of the pharmacological tests are given in the table in which the therapeutic indices (EDdr / LDdd) of the tested compounds are also given, as well as the ratio of the therapeutic indices (the therapeutic index of compound 1: the therapeutic index of lidocaine)
    Good results were obtained when studying the antianginal and antiarrhythmic effects of the compounds. I guinea pigs, which were previously injected intravenously with 1 mg / kg of ouabaina, in order to cause heart rhythm disturbances.
    Compounds 1 do not have a blocking effect on the p-receptors, although in their local anesthetic effect they are close to lidocaine. It is particularly beneficial that compounds 1 also have calcium ion antagonist properties. The antagonistic effect on calcium ions (pA,) of 3-methyl-7-methyl-961- (4-chlorobenzoyl-oxy) -3,7-diazabicyclo (3.3.1) dihydrochloride (3.3.1) nanoane has approximately the same magnitude , as in Verapramil, a compound successfully used in therapeutic
    1, 1539,00,029

    0,952,00,017
    1,221,00,057
    five
    : practice (4.33-4.6 for the proposed substance and 4.58-4.7 for verapramil),
    It has also been studied how the compounds affect the electrophysiological parameters of the heart. It was found that the new compounds do not have an irritating effect and increase the stimulation threshold, the duration of the impulse conduction and the refractory period, thereby affecting the stimulus-developing and impulse-driving system of the heart and the elimination of heart rhythm disturbances.
    The most likely therapeutic doses of compounds 1 when administered intravenously vary in the range of 0.5-1.0 mg / kg, and when administered orally} is about 10 mg / kg. This amount of active agent can be administered to the patient either once or in several doses, per day, depending on the nature and severity of the heart rhythm disorders.
    3-metsh1-7-ztil-9- - (4-chlorobenzoyloxy) -3, -7-d, and azabicyclo (3.3.1) nonane dihydrochloride is a substance for which the ratio of ED in oral administration to ED in intravenous administration is Em 16.7 seems to be particularly suitable for oral administration.
    0
    five
    12
    21
    3-methyl-7-ethyl-9o1- (4-chlorophenoxy) -3,7-diazabicyclo (3.3.1) nonane dihydrochloride
    3-Methyl-7-eth1-9o1 .- (2-chlorophenoxy) -3,7-diazabicyclo (3.3.1) nonane dihydrochloride
    Structural analogue of N, N -dibenzylbispidine
    Lidocaine
    Editor M. Tsitkina
    Compiled by I. Korsakova Tehred: G. Gerber Proofreader; L. Patay
    Order 1623/61 Circulation 379 Subscription VNIIPI USSR State Committee
    for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab ,, d, 4/5
    Branch ShSh Patent, Uzhgorod, 4 Project St.
    Continuation of table 5
    1.25
    41.0
    0.030
    12
    1.15
    28.0
    0.041
    22 10,028,50,3511
    权利要求:
    Claims (1)
    [1]
    A method for producing bicyclic compounds of the general formula I wherein R and R are methyl or ethyl group;
    R, 3 is an esterified hydroxyl group of the formula OR, where fefe, nil, unsubstituted or substituted by halogen, benzhydryl, or stereoisomers of these compounds or their pharmaceutically acceptable with acids, as long as the compound is common forl from a mule 0 I it / where R 4 and R 2 have the indicated meanings, in a dimethylformamide medium is reacted with sodium hydride and a compound of the general formula
    R ** X
    1 / where R has the indicated meanings;
    X is halogen, and, if necessary, compounds of the general formula G are converted into pharmaceutically acceptable salts.
    类似技术:
    公开号 | 公开日 | 专利标题
    US5451587A|1995-09-19|Quinuclidines, their use as medicaments and processes for their preparation
    CH643736A5|1984-06-29|PHARMACEUTICAL PREPARATIONS CONTAINING IMIDAZOLE DERIVATIVES OR THEIR SALTS.
    CH636096A5|1983-05-13|BICYCLIC PROSTAGLANDINE, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL PREPARATIONS.
    SU1222197A3|1986-03-30|Method of producing bicyclic compounds or stereoisomers of the compounds or their pharmaceutically acceptable salts with acids
    DE1518452C3|1973-10-04|4 substituted 2 benzhydryl 2 butanol derivatives and process for their preparation
    US8207192B2|2012-06-26|Quinuclidine compounds having quaternary ammonium group, its preparation method and use as blocking agents of acetylcholine
    DE3314878C2|1993-09-23|
    DD229407A5|1985-11-06|METHOD FOR THE PRODUCTION OF PIPERIDINDE DERIVATIVES, WHICH, AS MYOCARD PROTECTION, HAVE AN ANTIARRHYTMIC ACTIVITY
    CH638510A5|1983-09-30|PROSTACYCLINANALOGA.
    DE3625738A1|1988-02-11|2-ACYLOXYPROPYLAMINE DERIVATIVES, METHOD FOR THE PRODUCTION AND THEIR USE
    CH636353A5|1983-05-31|ENOLAETHER AND METHOD FOR THE PRODUCTION THEREOF.
    FR2503705A1|1982-10-15|PHENETHANOLAMINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
    EP0004335A2|1979-10-03|Prostacyclin analogs, process and intermediates for their preparation and their use as medicines
    US4478841A|1984-10-23|3-[2-|-ethyl]-indoles and their use as medicaments
    EP0013955A1|1980-08-06|Analogues of prostacyclin, their intermediates, a process for their preparation and medicaments containing them
    US3825590A|1974-07-23|Hydroxy-hydroxymethyl-substituted phenylalanine derivatives
    US4594421A|1986-06-10|Imidazopyridine compounds
    DE2828738A1|1979-02-01|ALPHA -HALOGENMETHYL-AMINOSAEUREN AND METHOD FOR THE PRODUCTION THEREOF
    US3317526A|1967-05-02|Omega-tertiaryamino butynol-1-phenylcycloalkane carboxylates
    US4792553A|1988-12-20|Diene derivatives and vasodilators containing the same
    EP0014996B1|1982-04-28|Heterocyclic spiro-amidines, their stereoisomers and optical isomers, methods for their preparation and medicaments containing them
    US4503058A|1985-03-05|Therapeutically useful 3,7a-diazacyclohepta[j,k]fluorene derivatives
    US3022310A|1962-02-20|Beta-yohimbine and beta-yohimbic acid 17-esters
    DD141927A5|1980-05-28|PROCESS FOR THE PREPARATION OF 1,1-DISUBSTITUTED OCTAHYDROINDOLO SQUARE BRACKET TO 2,3-A CORNER CLAUSE TO CHINOLIZINES
    EP0462150B1|1994-09-07|Novel aryloxy alkyl amines, their production and medicaments containing them
    同族专利:
    公开号 | 公开日
    NO157421B|1987-12-07|
    PL135878B1|1985-12-31|
    MX159288A|1989-05-12|
    IL66277A|1985-08-30|
    SE8204393L|1983-01-21|
    SE450704B|1987-07-20|
    IL66277D0|1982-11-30|
    FI71320C|1986-12-19|
    CA1254208A|1989-05-16|
    ES520567A0|1984-05-01|
    HU184960B|1984-11-28|
    PT75265B|1984-07-02|
    US4451473A|1984-05-29|
    PL244329A1|1984-05-07|
    IT1190920B|1988-02-24|
    NL8202908A|1983-02-16|
    PL237566A1|1984-03-12|
    IN155994B|1985-04-20|
    SU1272990A3|1986-11-23|
    FR2510575B1|1986-02-07|
    DE3226921C2|1994-03-10|
    AU552770B2|1986-06-19|
    DK160875B|1991-04-29|
    GB2102801B|1985-03-27|
    FI822526A0|1982-07-15|
    DK160875C|1991-10-14|
    NO822485L|1983-01-21|
    DK319982A|1983-01-21|
    NO157421C|1988-03-16|
    PH18502A|1985-08-02|
    DD202575A5|1983-09-21|
    PT75265A|1982-08-01|
    ES8401972A1|1984-01-01|
    BE893891A|1983-01-20|
    IT8222448D0|1982-07-19|
    AR230447A1|1984-04-30|
    PL135814B1|1985-12-31|
    CH653032A5|1985-12-13|
    CS235302B2|1985-05-15|
    AT379809B|1986-03-10|
    YU157182A|1986-10-31|
    FR2510575A1|1983-02-04|
    ATA272382A|1985-07-15|
    AU8617682A|1983-01-27|
    FI71320B|1986-09-09|
    DE3226921A1|1983-02-10|
    YU45867B|1992-09-07|
    FI822526L|1983-01-21|
    SE8204393D0|1982-07-19|
    ES8404354A1|1984-05-01|
    JPS5849383A|1983-03-23|
    GR76874B|1984-09-04|
    GB2102801A|1983-02-09|
    ZA824809B|1983-04-27|
    ES514126A0|1984-01-01|
    JPH0352465B2|1991-08-12|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    RU2503663C2|2007-04-27|2014-01-10|Актелион Фармасьютиклз Лтд|Bridge six-member cyclic compounds|US3078272A|1963-02-19|N-aza-bicyclo-alkylene-imino |
    DE2428792A1|1974-06-14|1976-01-02|Knoll Ag|NEW ANTIARRHYTHMICS|
    DE2726571A1|1977-06-13|1978-12-21|Basf Ag|NEW BISPIDINE DERIVATIVES, PROCESS FOR THEIR MANUFACTURING AND MEDICINAL PRODUCTS CONTAINING THEM|US5036153A|1989-05-11|1991-07-30|Braish Tamim F|Preparation of 2,5-diazabicyclo[2.2.1]heptanes and intermediates|
    GB9726630D0|1997-12-18|1998-02-18|Glaxo Group Ltd|Kv2.1 Antagonists|
    AU1996301A|1999-12-14|2001-06-25|Neurosearch A/S|Novel heteroaryl-diazabicycloalkanes|
    AU2005228289B2|2004-03-31|2008-01-10|Nippon Soda Co., Ltd.|Cyclic amine compound and pest control agent|
    SI1947098T1|2005-10-06|2012-02-29|Nippon Soda Co|Cyclic amine compounds and pest control agent|
    UA86328C2|2005-10-06|2009-04-10|Ниппон Сода Ко., Лтд.|Bridged cyclic amine compound and pest control agent|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    HU812112A|HU184960B|1981-07-20|1981-07-20|Process for preparing new derivatives of 3,7-diazabicyclo/3.3.1/ nonane|LV930048A| LV5259A3|1981-07-20|1993-01-18|Saturation of Bicyclic Compounds or Stereoisomers of Bicyclic Compounds or Compounds thereof, or a pharmaceutically acceptable salt thereof|
    [返回顶部]