• 专利附录
  • 专利说明
  • 权利要求
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    • 专利摘要:
    1. A process for the preparation of prostadcycline derivatives of the general formula iH A-C-B or their epimers, where R is hydrogen, alkali metal or lower alkyl; 1 is hydrogen or methyl; --CH -CH--, trans-CHA CHA y-, trans-1-nn-; 1 ((CKl}, - SU (or –C (P in the hegexyl cycle; 1 and R are the same or different, hydrogen or ethyl), and with the fact that the compound of the general formula OH is J.) and R2 have the indicated values where A, B Y and the same or different, R are hydrogen, or the protective group of tetrahydropyranyl or trimethylsilyl, is reacted in an organic solvent medium in an inert atmosphere at 0-30 ° C in the presence of a strong base with 1-6 {SbH5) sR-Sh2-O 1, in Hai 41 I-Ch41LPT 6 JOOR where in is hydrogen, methyl or ethyl; Hal is bromine or d, 6 and then, when K is hydrogenated, is esterified with diazomethane at 0-30 ° C, and when R and R 5 are a protective group, the latter are split off to give the compound of the general formula OH a S but soov A-C -BCO2 where R, .A and B have the indicated values: R- methyl or ethyl, which: is brominated or iodinated in the presence of an inert solvent and, if necessary, in the presence of an acid acceptor at 0-30 s and cycled into a compound of the general formula. where t, I, A and B have the indicated meanings; X is bromine or iodine, and halogen-water is split off from the resulting compound of the formula B at 0-90 ° C.
    公开号:SU1072801A3
    申请号:SU813314353
    申请日:1981-08-07
    公开日:1984-02-07
    发明作者:Зайпп Ульрих；Фолленберг Вернер；Мюллер Бернд；Михель Гудрун
    申请人:Грюненталь Гмбх (Фирма)；
    IPC主号:
    专利说明:

    genus 1-5 times the number of bases and, if necessary, in the resulting compound of the general formula
    COOR
    A-C-B:
    HOV
    where R, R, A, and B have the indicated values, the ester group in the aqueous alcohol solution is washed with an alkali metal hydroxide at 10-50 ° C, and the resulting target products are separated and, if desired, separated into 5E and 5z isomers by liquid chromatography under high pressure.
    2. A method according to claim 1, characterized in that the reaction of the compound of formula P with the compound of formula III is carried out with the addition of catalytic amounts of benzoic acid.
    3. Method POP1, characterized in that halogenated and cyclizing a compound of the formula fV iodine, potassium iodide or bromosuccinimide are used, if necessary in the presence of water and sodium bicarbonate magnesium oxide or calcium carbonate.
    4. The method according to claim 1, about tl and h ay shchi and the fact that the sodium hydroxide, potassium hydroxide or 1,5-diazabicyclo (4,3,0) -non-5- en.
     , ; ,:; The invention relates to a process for the preparation of new derivatives of prostacyclins of a general formula, but BUT R2 epimers, is hydrogen, alkali metal: at tall or lower alkyl R is hydrogen or methyl; A -., Trans-CK 3 4 MCH2) e-CH3 or cyclohexyl; R and R are the same OR different hydrogen or ethyl with valuable pharmacological properties. The known method of obtaining simple glandinov of the series and E2 by condensation of y-lactol with the corresponding triphenylphosphonium halide according to Witt in an inert organic solvent medium in the presence of a strong base of Cu. The purpose of the invention is to obtain new prostacyclin derivatives, which allowed the expansion of the arsenal of tools to a living organism, with improved properties compared to the closest structural analogues, for example PGF2o (, This goal is achieved by the fact that the compound of the general formula :( AMJ-B R have the indicated meanings A, B and neither i are the same or different, hydrogen or the protective group — tetrahydropyranyl or trimethylsilyl is reacted in an organic solvent medium in an inert atmosphere with in the presence of a strong base 1-b multiple molar amount of the compound of the general formula Iv yjjtfM. / - 1., e, G (SbH5) s®-CH, L where R is hydrogen, methyl or ethyl; Hal is brpm or iodine, and then R is hydrogen, is esterified with diazomethane at 0-30 ° C, and when R and R are a protective group, the latter are cleaved to give a compound of the general formula A-C-B OOR, but where R2, A and B have the indicated values; R is methyl or ethyl, which is brominated or iodinated in the presence of an inert solvent and, if necessary, in the presence of an acid acceptor, when and cyclized into a compound of the general formula -4Г О-j-dH- - Chook NO R1 15 co union of in 2 mL of diethyl ef pa. The reaction mixture was stirred for 45 min. At dark and stirred at room temperature, and then treated with sodium thiosulfate solution. The colorless reaction mixture is poured into a nasic ice-cold solution of sodium chloride and extracted three times thoroughly by shaking with 20 ml of diethyl ether each time. The ether phase is dried over magnesium sulphate, filtered and in a cold state in the dark under vacuum, concentrated on a rotary ISPA Itel. The raw material obtained in the form of a yellow oil (180 mg, P 0.58, ethyl acetate) is processed without further purification. t) Methyl ether C (5EZ, 13E, 9e, Hot, 155) -2,3,9-trinor-1,5-inter-mphenylene-B, 9-zpoxy-11,15-Dioxy-15methylZ-simple-5 , 13-diene acid General formula I; And trins ns nn- | v -n-SdNu ,. 180 mg of the compound described in Example 1 are dissolved in 2 ml of toluene, diluted with 100 µl of DBN and stirred in the dark for 4.5 hours. Toluene is blown away with nitrogen at room temperature. The residue after column chromatography on silica gel with ethyl acetate gives 90 mg of a yellowish oil consisting of two components. R 0,55 and 0,6 (ethyl acetate). ) Sodium salt of l (5EZ, 13E, 9 (3i Hoi., 15S) -2,3,4-trinor-1,5-inter-LAphenylene-b, 9-epoxy-11,15-dioxy-15-: methylJ -npocTa-5,13-diene acid General formula I: R Na, R r-CHj A-Tr "ns-CH CH-; B.,.,. §0 mg of 1 g of the compound obtained in Example is dissolved in 1 ml methanol, diluted with 600 µl of 1N NaOH is stirred at 30–40 ° C for 12 hours. R 0.36 and 0.44 (silica gel RP methanol - water 80:20). Liquid chromatography, high pressure methanol-water 40/60 on silica gel after freeze-drying, gives: 1) sodium salt of C (5Z, 13E, 9ot, Hot, 15s) -2,3,4-trinor-1,5-inter- "phenylene b, 9-EPOXI-11,15 -dioxy-15methyl -simply-5, 13-di Enoic acid Yield 35 mg, Rr 0.36 {silica gel, methanol-water 80:20). H-NMR (methanol-a.): 0.9, t, 3N; l, 28, s, 3N; 3.63-4.2%, 1H) 5.28 S expanded, 1H, - 5.55-5.73, t, 2H; 7.06-7.48, t 2H, 7.53-5.8, t, 2H; 7.96-8.1, t, 1H. ii) sodium salt (5E, 13E, 9ot, llfli, 158) -2,3,3-trinor-1,5-inte-M-phenylene-6,9-epoxy-11.15-dioxy-15-methyl-prost-5, 13 -diene acid. Yield 18 mg, Hf 0.44 (silica gel RP-8, methanol-water 80:20). H-NMR (methanol-d) 0.9, t, 3N; 1.3, S, 3N; 3.56-4.16, m, 1H) 5.55, 7, t, 2H, 5.9, s expanded, 1H; 7.13-7.48, m, 2H; 7.53-7.9, m, 2H. PRI mme R 2. Using the method described in Example 1, the corresponding starting materials give: a) sodium salt G (5E, 13E, 9oL, Hod, 158) -2,3,4-trinor-1,5- interphenylene-6, 9-epoxy-11,15-dioxy} is simple-5, 13-diene acid. General formula I: p Na; hydrogen A -tryns-CH SYa-; B - n-CjH H-NMR (methanol-a): 0.9, lt, 3N; 1.3, s., NN; 3.6-4.15, t, 2K; 5.5-5.7 t, 2H, 5.86-6.05, S expanded, 1H; 7.15-7.5, t, 2H {7.58-8, m, 2H. Wg 0.44 (silica gel RPs8, methanol-water 80:40). b) sodium salt (5z, 13E, 9oi, iloi, 15s) -2,3,4-trinor-1,5-inter-A "phenylene-b, 9-epoxy-11,15-dioxy-prosta-5, 13-diene acid. General I: p Na R hydrogen; A -tr "Hc-CH CH-; B - H-NMR (methanol-a4): 0.9, t, 3N; 3.5-4.1, t, 3N; 5.25, S expanded., 1H; 5.45-5.7, t, 2K; 7.7.5, t / 1H, 7, 5-7.85, m,., S, expanded ,, lH, j Cl 0.34 (silica gel RP-8, methanol-water 80: 20). Example 3. Analogously to the method described in example 1, from m-carboxyphenyl-methyl-triphenylphosphonium bromide and the corresponding compound of formula II, a) sodium salt (5E, 13E, Bet-, lleL, 15z) -2,3, .4 is obtained. -trinor-1,5-interl-phenylene-b, 9-epoxy-11,15-dioxy-15cyclohexyl-16, 17,18,19,20-pentanor simple-5,13-diene to the acid. General formula i: R Na, R hydrogen; A-France-CH CH-; B - cyclohexyl. H-NMR (methanol-d.): 3.65-4.1, t, 3N; 5.5-5.7, m, 2H; 5.97, s expanded., 1H, 7.2-7.5, m, 2H; 7.5-8, t, 2H. Rf 0.52 (silica gel RP-8, methanol-water 80 .: 20). b) sodium salt of f (5z, 13E, 9ei, Hot, 158) -2,3,4-trinor-1,5-inter-l phenylene-6, 9-epoxy-11,15-dioxy-15g cyclohexyl-16 , 17,18,19,20-pentanorJprost-5, 13-diene acid. General formula i: Ri Na; in, dorod; And - rpoiHC-CH CH-; B - cyclohexyl. H H-NMR (methanol-a) 3.67-3.95, t, 2H; 4-4.2, m, 2H) 5.37.5, enlarged, 1H / 5.5-5.7, m, 2H; 7.15-7.4, y, 1H; 7.6-8.15, m, 3N. R "0.38 (silica gel RP-8, methanol-water 80:20). Example 4. Using the above methods in the above examples, the following are prepared: a) USE sodium salt, 13E, 11, -158, 16RS) -2,3,4-TpHHOp-1, 5-HHter-m-phenylene-b, 9-epoxy-11,15- Dioxy 1b-et1 | l-simple-5,13-diene acid Obpa formula itR - Ma; vodorod, - A-Grans-CH "CH-; B — CfR, R) - (CH 2) 3CHj, where R C is water H-NMR (methanol-d4) 0.9, t, bN; 3.6-4.2, t, ЗН; 5.5-5.7, m, 2H / 5.95 S dilated, 1H; 7.15-7.35, m, 2H; 7.6-7.95, m, 2H. Rf 0.68 (silica gel RP-8, methanol-water 80:20). b) sodium salt (5Z, 13E 9eL, Hot 15s, 16RS) -2,3,4-TpHHOp-l, 5Invr-m-phenylene-6, 9-epoxy-11,15 DIOXI-16-ETHIL iJ-process-5 , 13-dienoic acid. The general formula I: R is hydrogen, - A-Tp «ns-CH CH-; B - CHCCjlU- (СН2), - СНз. % NMR (methanol-a4): 0.9.1, 6H, 3.75-4.55, and, 3N; 5.35.3, expanded. 1 TO; 5.5-5.7, ™, 2H, - 7.1-7.4, t, 1I; 7.55-7.95, m, 1H, - 8.05, m, IH. Y - i f f Ш f f. 1l f f - f at f Rr 0.68 (Silkkagel RP-8, MeTanol-water 80:20). Example 5. Starting from M-carboxy-phenylmethyl-triphenylphosphonium bromide and ZoC5o-dioxy-2 - (3RS) -3oxy-1-octyl3-1ticlopentane-1c (-acetaldehyde- | -lactol-bis-tetrahydropyranyl ether in the manner described in Example 1 / receive: a) sodium salt (5E, 9 ° C, 11 °, 15BS) -2,3,4-trinor-1,5-inter-mphenylene-6, 9-epoxy-11,15-dioxy Jiprota-5-new acid. l: R Nfi, hydrogen; A - -sNg-sng -, - in -n -SuN. % NMR (methanol-a4): 0.9, t, 3H 5.9, S expanded, IH; 7.18-8.15, m, 4Hf no signal at 5.5-5.7. R 0.48 (silica gel RP-8, meta “ol-water 80:20).
    Relative
    1.0 exposure Table 2 shows the relative effect on thrombocytopenia in vivo on anesthetized rat, 45 10
    0.86
    1.2
    1.2 18.0
    0.31 1 ft) sodium salt t (5z, 9ei, llci, 15RS) -2,3,4-trinor-1,5-inter-l-phenylene-6, 9-EPOXI-11,15-dioxy-prost -5-enoic acid. Na; In general, the formula I: R Prenatum; And - - SNG-SNG-; 3 - H-NMR (methanol- (14): 0.9, t, 3N; 5.3, S expanded., 1H; 7.1-8.05, ha, 4H; no signal at 5.5-5 , 7. Rf 0.41 (silica gel RP-8, metag 80:20). Compounds of formula I affect platelet aggregation in vitro and in vivo, as well as blood pressure in the same way as acyclin, but they differ from prostacyclin. stability. Compared with 5,6-dihydroprostacyclin used as a chemically stable reference substance, the product of example 35 is many times higher than the effect of the comparative substance. In the substances obtained according to the invention In addition, an active ratio of the inhibiting platelet aggregation to blood pressure lowering activity was unexpected: as opposed to 5,6-dihydroprostacycl in which both effects appear at the same doses, while using compounds of Formula I, the effect of lowering blood pressure is observed only at higher doses than the effect inhibiting the aggregation of trismocytes, which is confirmed by the data of Tables 1–4, in which some substances of Formula I are given experimentally (in experiments on groups of 4-6 animals) by the obtained data of relative efficiency in comparison with 5,6-dihydrprostacyclin. . Table 1 shows the relative effect on human platelet aggregation in vitro, induced by arachidonic acid (LCjjj means a concentration that in 50% of cases under the conditions of the experiment does not allow platelet aggregation, for 5 6-dihydroprocyclcycline is 0.18 0, 18 µmol / l) .. induced by adenosine diphosphoric acid (LDF), anesthesia with urethane, administration of the test substances is internal.
    An EUt for 5; b-dihydroprostacyclin under these conditions of experience is 0.0114 mg / kg.
    Table 2 Relative. impact, 1.0 0.97 1; 3 5.0 0.2 tvii It should be noted that the product of example 3, both in vitro (Table 1) and in vivo (Table 2), is much more effective than p 5, b - dihydroprostacyclic on. Table 3 shows the relative effect of reducing blood pressure on non-narcotized rats with spontaneous hypertension; measuring with a constant catheter, intravenous application of the test substances; for 5,6-dihydroprost cyclin, under these conditions the test is 0.005 mg / kg. Table 3 Relative impact, 014 0.1 0.25 0.0 SST 1.0 Table 4 shows the selectivity index / action, inhibitory aggregation effect, lowering blood pressure / compared to 5,6-dihydroprostatic (calculated from the data of Table 2 and 3). From these data it follows that the compounds of formula 1 can be used both in diseases in which it is desirable to inhibit aggregation without a decrease in blood pressure (for example, hyper-aggregability in coronary heart disease), and in higher doses in diseases which it is advisable concomitant vasodilator action (for example, in case of blockage of the peripheral arteries). Natural prostacyclin, as well as chemically stable 5,6-dihydroprostacyclin, in vivo has only a short-term effect, inhibiting aggregation and reducing blood pressure. Therefore, these compounds can be used for therapeutic purposes only as a long-term intravenous infusion. In addition to the spontaneous hydrolytic inactivation of natural prostacyclin, the mechanisms of inactivation, which only lead to the short duration of action of even chemically stable 5,6-dihydroprostacycline in vivo, are currently only partially clarified. The compounds of formula I have a longer duration than 5,6-dihydroprostacyclin, which means that, as follows from Table 5 and b, they are also suitable for achieving long-term effects, slowing down aggregation and reducing blood pressure after taking single doses. Table 5 shows the duration of action. Inhibition of platelet aggregation in vivo (measured on a model of ADP-induced thrombocytopenia in an anesthetized rat by intravenous administration of the test substances). The tabl.b shows the results of the action that lowers blood pressure,
    Tables a5 on non-narcotized rats with spontaneous hypertension. I-table b
    权利要求:
    Claims (4)
    [1]
    1. A method of obtaining derivatives of prostacyclin of the general formula where R4 is hydrogen, methyl or ethyl; Hal is bromine or iodine, and then, when R 6 is water-ether, it is esterified with diazomethane at 0-30 ° C, and when R ^ and RU are a protecting group, the latter are cleaved to give a compound of the general formula
    BUT'
    A-C-B H0 ZX R 2 epimers,
    - hydrogen, alkali metal or lower alkyl;
    - hydrogen or methyl; -CH - CH g -, trans-CH = CH-; -C (P -) (R 4 ) - (CH,), - CH 'or cyclohexyl; 3 a ggi. R 4 is the same or different, hydrogen or ethyl, and so on, a compound of the general formula
    OH or them where R 1
    And B - that where A A and B have the indicated meanings; R 7 is methyl or ethyl, which is brominated or iodinated in the presence of an inert solvent and, if necessary, in the presence of an acid acceptor at 0-30 ° C and cyclized to a compound of the general formula
    B and R 2 have the indicated meanings of R y and R y * - the same or the same where R 2 , R 7 , A and B have the indicated meanings;
    X is bromine or iodine, and halide-water SU 1072801 genus of 1-5 times the amount of base and, if necessary, the resulting compound of the General formula are removed from the obtained compound of the formula y at 0-90 ° C
    A-C-B but R2 where R 2 , r a and B have the indicated meanings, saponify the ester group in an aqueous-alcoholic solution with alkali metal hydroxide at 10-50 ° C, and the obtained target products are isolated and, if desired, separated into 5E- and 5Zomers using high pressure liquid chromatography.
    [2]
    2. The method according to claim 1, characterized in that the interaction of the compounds of formula P with the compound of formula f is carried out with the addition of catalytic amounts of benzoic acid.
    [3]
    3. The method according to claim 1, characterized in that. For halogenation and cyclization of the compounds of formula IV, iodine, potassium iodide or bromosuccinnimide are used, if necessary, in the presence of water and sodium bicarbonate, magnesium oxide or calcium carbonate.
    [4]
    4. The method according to claim 1, characterized in that when the removal of hydrogen halide, sodium hydroxide, potassium hydroxide or 1,5-diazabicyclo- (4,3,0) non-5-ene are used as the base.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
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    DE2902809A1|1979-01-25|1980-08-07|Hoechst Ag|NEW PROSTACYCLIN ANALOGS|IL65387D0|1981-04-14|1982-05-31|Chinoin Gyogyszer Es Vegyeszet|2,3,4-trinor-m-inter-phenylene-prostaglandin derivatives and a process for the preparation thereof|
    IL67332A|1981-12-01|1985-12-31|Chinoin Gyogyszer Es Vegyeszet|Inter-m-phenylene-prostacyclin analogues,process for the preparation thereof and pharmaceutical compositions containing them|
    HU188559B|1981-12-01|1986-04-28|Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu|Process for preparing new inter-m-phenylene-prostacyclin derivatives|
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    DE3317159C2|1982-05-27|1992-02-06|Gruenenthal Gmbh, 5100 Aachen, De|
    DE3914735A1|1989-05-05|1990-11-08|Gruenenthal Gmbh|PHARMACOLOGICALLY ESTER, THE MEDICAMENTS CONTAINING THEM AND THE MANUFACTURE OF THIS ESTER AND MEDICAMENT|
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