CN1031232A - Etoposide glucoside 4 '-phosphate derivative and preparation method thereof - Google Patents

Abstract

The present invention relates to new antineoplastic agent 4 '-phosphate derivative and the salt thereof of demethylation Etoposide glucoside, their preparation method.This class novel anti-tumor medical instrument has highly water-soluble.

Description

Etoposide glucoside 4 '-phosphate derivative and preparation method thereof

The part continuation application of the application's U.S. Patent Application Serial 081,493 that to be on August 4th, 1987 submit to United States Patent (USP) trademark office.

The application relate to Etoposide glucoside 4 '-phosphate derivative, their antitumor application and contain the pharmaceutical composition of these new medicaments.Etoposide formaldehyde glucosides (Etoposide, VP-16, I) and Etoposide thiophene aldehyde glucosides (teniposide, VM-26, II) is the carcinostatic agent of clinical use, to make by naturally occurring lignanoid Etoposide (III), this compounds that comprises Etoposide formaldehyde glucosides and Etoposide thiophene aldehyde glucosides is called 4 sometimes '-demethylation Etoposide glucoside.Etoposide formaldehyde glucosides and Etoposide thiophene aldehyde glucosides comprise carcinoma of testis in treatment, small cell lung cancer, and ovarian cancer, mammary cancer, thyroid carcinoma, bladder cancer, brain tumor, non-lymphocytic leukemia, various cancers such as Hokdkin disease aspect is effective.

Chemical compounds I and II and production method thereof are disclosed in United States Patent (USP) 3,408 by Wartbury etc., 441 and Kellev-Juslen etc. be disclosed in United States Patent (USP) 3,524,844.Compound wherein particularly Etoposide formaldehyde glucosides and Etoposide thiophene aldehyde glucosides as the present invention prepare Etoposide glucoside 4 '-raw material of phosphate derivative.

The phosphorylation of hydroxyl therapeutical agent has been used as a kind of means of drug latenciation; Phosphorylated derivative discharges the reactive precursor molecule through the phosphoesterase cracking in vivo.(Sinkula and Yalkowsky, Jphavm.Sci 1975,64, in comment 181-210) for " principle of design of biological reversibility medicaments derivative: prodrug " to be included in exercise question as the short discussion of potential prodrug.The example of the phosphoric acid ester of known antitumour drug has camptothecine (the open 21-95 of Japanese Patent, 394 and 21-95,393; Derwent Abst. № 87-281016 and 87-281015) and zhengdingmeisu (United States Patent (USP) 4,185,111).

Podophyllotoxin organic phosphate disodium salt IV is made by Seligman etc.But this phosphoric acid ester can not be through prostate acid phosphatase hydrolysis and toxicity unlike parent Etoposide low (Cancer chemotherapy Reports I, 1975,5: 233-242).

The invention provides have 4 of anti-tumor activity '-phosphoric acid ester of demethylation Etoposide glucoside.Particularly, 4 '-the dihydrogen phosphoric acid ester of demethylation Etoposide glucoside and salt thereof are water-soluble strong, in having provided existing this class therapeutical agent Etoposide formaldehyde glucosides of a kind of ratio and the better medicament of Etoposide thiophene aldehyde glucosides (water-soluble little).

The invention provides 4 of general formula V '-demethylation Etoposide glucoside 4 '-phosphate derivative and pharmacy acceptable salt thereof,

R in the general formula ⁶Be H; R ¹Be to be selected from (C _1-10) alkyl, (C _2-10) alkenyl, (C _5-6) cycloalkyl, 2-furyl, 2-thienyl, (C _6-10) aryl, (C _1-14) aralkyl and (C _8-14) arylalkenyl, these aromatic rings can not replace or be substituted with one or more fontanel element, (C of being selected from _1-8) alkyl, (C _1-8) alcoxyl alkane, hydroxyl, nitro and amino group; Or R ¹And R ⁶(C respectively does for oneself _5-6) alkyl; Or R ⁷And R ⁸Coupled carbon atom forms (C together _5-6) cycloalkyl; X is oxygen or sulphur; R ⁷And R ⁸Be selected from H independently of one another, (C _1-5) alkyl, A-replaces (C _1-5) alkyl, (C _3-6) cycloalkyl, A-replaces (C _3-6) cycloalkyl, (C _6-10) aryl, A-substituted aryl, the aryl that alkyl replaces, (C _7-14) aralkyl, the aralkyl that aralkyl that A-replaces and alkyl replace; Here said A-substituting group is to be selected from hydroxyl, alkoxyl group, alkanoyloxy, cyano group, amino, alkylamino; dialkylamino, carboxyl, alkylthio, sulfydryl, mercapto sulfenyl; nitropyridine base disulfide base, alkyl amido, alkyloyl, formamyl, one or more groups of nitro and fontanel element.

The salt of compound V comprises single anion salt and two anion salts.Positively charged ion can be for example basic metal or alkaline-earth metal ions or other plain metal ion of metal ion; Or organic nitrogen-containing base ammonium for example, one, two or three alkane ammonium or pyridiniums.Positively charged ion preferably is selected from sodium, potassium, lithium, caesium, magnesium, calcium, aluminium, ammonium and, two and three alkane ammoniums.Preferred version provides R ⁷And R ⁸All be acceptable salt on the general formula V compound of H and the pharmacology thereof.Preferred plan provide Etoposide formaldehyde glucosides 4 '-dihydrogen phosphoric acid ester and thiophosphatephosphorothioate and corresponding disodium salt VI a and VI b.

Another preferred version provides R ⁷And R ⁸Identical and be selected from 2,2,2-three fontanel ethyls, 2-cyano ethyl, (C _1-5) alkyl, the general formula V compound of phenyl and phenylalkyl, the phenyl ring here is substituted with alkyl arbitrarily, fontanel element or nitro.

Another aspect of the present invention has provided the antitumor phosphoramidic acid ester derivative and the pharmacy acceptable salt thereof of general formula VII,

R in the general formula ¹, R ⁶With the definition of X as above; Y is Cl, H or NR ⁵R ⁶; R ², R ³, R ⁴And R ⁵Be selected from H independently of one another, (C _1-5) alkyl, (C _2-5) thiazolinyl, (C _3-6) cycloalkyl, (the C that A-replaces _1-5) alkyl, (the C that A-replaces _2-5) thiazolinyl, (the C that A-replaces _3-6) cycloalkyl; Or R ², R ³Be unified into 3-6 unit ring together with the nitrogen that is attached thereto; Or R ⁴, R ⁵Become 3-6 unit ring together with the nitrogen that is attached thereto; Here said A-substituting group definition as above.

Another aspect of the present invention provides the dichloro phosphoric acid ester intermediate of general formula VIII, wherein R ¹, R ⁶With the definition of X as above; These intermediates are useful in preparation general formula V compound.

Further aspect of the present invention has provided preparation R ⁷And R ⁸All be the general formula V compound of H and the method for pharmacy acceptable salt thereof, this method comprises that (a) is converted into the compound of general formula X, wherein R with the compound of general formula IX ¹, R ⁶With the definition of X as above, G is the phosphoric acid ester protecting group,

(b) remove the phosphoric acid ester protecting group, (c) product that at random (b) is gone on foot is converted into pharmacy acceptable salt.The phosphoric acid ester protecting group comprises top R ⁷Those groups (except the H) of definition, but be not limited to this.

Except as otherwise noted, terminology used here " alkyl " refers to the straight or branched alkyl; " fontanel element " refers to bromine, chlorine, fluorine and iodine; " etopofos " be meant Etoposide formaldehyde glucosides 4 '-organic phosphate disodium salt (be the compound VI a).

4 '-phenolic group of demethylation Etoposide glucoside can turn to corresponding dichloro phosphoric acid ester and dichloro thiophosphatephosphorothioate (general formula VIII) by phosphoryl chloride and thiophosphoryl chloride phosphinylidyne.This phosphorus acylation reaction is preferably in and tertiary amine base such as N in suitable anhydrous organic solvent such as acetonitrile, and the N-diisopropylethylamine carries out under existing.Reaction process can be used thin-layer chromatography (TLC) monitoring, i.e. the disappearance of appearance by product and raw material or both come together to judge optimum reacting time.The empirical response cycle according to us can be from about 4 hours to 72 hours.As if the length in required reaction times relevant with the quality of used phosphorus reagent.

4 of general formula VIII '-the dichloro phosphoric acid ester is multiduty intermediate, can obtain various phosphoric acid ester and phosphorothioate derivative with the nucleophilic reagent reaction afterwards.This intermediate hydrolyzable is phosphoric acid ester and obtains phosphoric acid salt in the presence of alkali.For example, general formula VIII compound with the excess bicarbonate aqueous solution handle obtain corresponding 4 '-disodium phosphate and 4 '-the thiophosphatephosphorothioate disodium salt.The supercarbonate of other positively charged ion such as potassium and ammonium also can be used for providing corresponding salt.Dichloro phosphoric acid ester intermediate VIII can generate corresponding di(2-ethylhexyl)phosphate carboxylic acid amide esters or chlorine mono phosphoric acid ester carboxylic acid amide esters with the amine reaction.Suitable amine comprises ammonia, primary amine such as ethamine, chlorethamin, allylamine, dimethylaminopropylamine, oxyethylamine, hexahydroaniline and Trans-4-Amino Cyclohexanol, and secondary amine such as diethylamine, piperidines, ethylmethylamine, methylethylolamine, N-Ethylbutylamine etc., but be not only limited to these.The amine amount used with respect to Etoposide dichloro phosphoric acid ester can be regulated so that help the generation of one or another kind of reaction product.For example, when using more excessive amine with respect to Etoposide, obtaining symmetric di(2-ethylhexyl)phosphate carboxylic acid amide esters is that Y also is NR in the general formula VII ²R ³Compound; When using the amine of manipulated variable, obtain chlorine mono phosphoric acid ester carboxylic acid amide esters, promptly Y is the compound of chlorine in the general formula VII.Chlorine mono phosphoric acid ester carboxylic acid amide esters hydrolyzable is that Y is the compound or its salt of OH in the general formula VII, and perhaps it can further obtain asymmetric di(2-ethylhexyl)phosphate carboxylic acid amide esters with the secondary amine reaction, and promptly Y is NR in the general formula VII ⁴R ⁵Rather than NR ²R ³Compound.

Above-mentioned reaction process can be with following reaction formula explanation.

Phosphotriester is R in the general formula V ⁷And R ⁸Be not the compound of hydrogen, these compounds can [be (OR of fontanel element-P(X) by the fontanel phosphodiester ⁷) (OR ⁸)] processing 4 '-preparation of demethylation Etoposide glucoside.Have found that, this be reflected in the presence of organic three alkanamine alkali, carry out in the acetonitrile the most effective.Only alkali is diisopropyl ethyl amine.The consumption of fontanel phosphoric acid ester and amine is monovalent at least, but compares with the consumption of Etoposide glucoside, and these two kinds of reaction reagents are the molar equivalent of the handy amount of skipping over.This reaction can be carried out under the temperature that product forms in any helping, as if but, high slightly temperature can be quickened the reaction that this will finish originally as 30～40 ℃ in a couple of days.Symmetric fontanel phosphodiester [is R ⁷=R ⁸] can prepare easily from pure and mild for example phosphoryl chloride, asymmetric fontanel phosphoric acid acid esters [is R ⁷≠ R ⁸] can be from pure and mild two fontanel phosphoric acid ester preparation.By other path of preparing phosphotriester also is possible, for example phenol by with (C ₆H ₅CH ₂O) ₂PN(i-C ₃H ₇) ₂Such reagent react becomes phosphorous acid ester earlier, is phosphotriester with for example this phosphorous acid ester of metachloroperbenzoic acid oxidation then.

Phosphotriester also can be used as the intermediate of preparation general formula V compound and its esters.For example, when diphenyl phosphate (in the V formula, R ⁷=R ⁸=phenyl) obtain during catalytic hydrogenation the dihydroxyl phosphoric acid ester (in the formula V, R ⁷=R ⁸=H).Other suitable phosphoric acid ester protecting group includes, but is not limited to 2,2,2-three chloroethyls, benzyl, cyanoethyl, phenyl, benzyl, styroyl and right-bromophenyl that right-nitro replaces.Dihydroxyl phosphoric acid ester (R in the formula V ⁷=R ⁸=H) with suitable alkali sodium bicarbonate for example, bicarbonate of ammonia or organic amine reaction are converted into salt.In addition, make this dihydroxyl phosphoric acid ester want cationic ion exchange resin column also can produce this salt by containing.

Though the present invention's phosphoryl chloride, fontanel phosphodiester and corresponding sulfur analogs thereof be as phosphorus esterification reagent, but also can use other phosphorus reagent of Pyrogentisinic Acid's phosphorylated, suitable reaction conditions and medium can be selected according to selected phosphorus esterification reagent.Exercise question be " modernism of biomolecules phosphorylated " (Synthesis, 1977, commentary article 737-52) has comprised the other example of phosphorus esterification reagent, therefore, is received in for referencial use here.

Representative compounds of the present invention is estimated anti-tumor activity with mouse transplantability P388 leukemia.In all tests, with 10 of P388 murine leukemia ⁶Ascites cells is inoculated in the female CDF mouse.Use in the test Etoposide formaldehyde glucosides 4 '-phosphoric acid ester, its disodium salt and 4 '-during the thiophosphatephosphorothioate disodium salt, tumor inoculation and pharmacological agent all are through intravenous injection.In other test, tumor inoculation and pharmacological agent are through abdominal injection at all.And in all tests, make positive control with abdominal injection Etoposide formaldehyde glucosides.Test duration 28-48 days, the number of mice of the whole survival in latter stage of record.Anti-tumor activity represents that with %T/C this is the ratio of the mean survival time (MST) of medication therapy groups to the mean survival time of brine treatment control group.

It is generally acknowledged that in P388 test, the %T/C value is 125 or bigger compound, has notable antitumor activity.Table 1 has been listed the result of above-mentioned evaluation.Report maximum %T/C value in the table and reached the dosage of such effect.

Table 1

To the leukemic anti-tumor activity of mouse P388

Compound dosage * approach MST(d) % T/C

(mg/kg/ injection)

Intravenously implantation tumour cell

Embodiment 1 140 veins 29.0 363

Etoposide formaldehyde glucosides 50 abdominal cavities 20.5 256

Embodiment 4 200 abdominal cavities 18.0 225

Etoposide formaldehyde glucosides 100 abdominal cavities 21.5 269

Embodiment 8 125 veins 24.5 306

Etoposide formaldehyde glucosides 100 abdominal cavities 29.5 369

Show 1-to continue-

Compound dosage * approach MST(d) % T/C

(mg/kg/ injection)

The intraperitoneal inoculation tumour cell

Embodiment 2 240 abdominal cavities 16.5 165

Etoposide formaldehyde glucosides 60 abdominal cavities 25.0 250

Embodiment 3 200 abdominal cavities 15.5 155

Etoposide formaldehyde glucosides 100 abdominal cavities 27.0 270

Embodiment 7 240 abdominal cavities 25.0 250

Etoposide formaldehyde glucosides 100 abdominal cavities 26.0 260

Embodiment 9 150 abdominal cavities 19.5 217

Etoposide formaldehyde glucosides 100 abdominal cavities 24.0 267

* as not illustrating in addition, is the 5th day and administration in the 8th day (the 1st day is the same day of tumor inoculation).

Confirmed already that antineoplastic compound of the present invention had the activity of anti-transplant tumor in laboratory animal.General formula VI a(" etopofos " particularly) compound of representative has than the much higher anti-tumor activity of Etoposide formaldehyde glucosides in the P388 test.This selectivity medicament has been represented the prodrug (anti-tumor activity that exsomatizes is low) of the Etoposide formaldehyde glucosides of a class highly water-soluble, disengages Etoposide formaldehyde glucosides through rapid decomposition of alkaline phosphatase.The Etoposide formaldehyde glucosides that disengages presents with the parent medicine same cytotoxicity.

Therefore, the invention provides a kind of method that suppresses mammal tumor, this method is with the general formula V of effective inhibition tumor dose or the antineoplastic compound of VII to tumor host.For this reason, can include but not limited to intravenous injection, intramuscularly, intratumor injection, injection and oral in the intra-arterial injection, lymph with the ordinary method administration.

Another aspect of the present invention has provided a kind of pharmaceutical composition, and said composition comprises the compound and the pharmaceutically acceptable carrier of general formula V and VII.This anti-tumor compositions can be constituted with any pharmaceutical dosage form that is appropriate to desired medicine-feeding way.The example of such composition comprises solid dosage such as tablet, capsule, pill, pulvis and the granule of oral administration, the preparation of the liquid dosage form of oral administration such as solution, suspension, syrup or agent and parenteral admin such as aseptic solution, suspension or emulsion; Also can make the aseptic solid composite form, this solids composition can be dissolved in sterilized water, physiological saline or other Injectable sterile medium before use.

About the optimal dose and the usage of mammals host administration, the people who is familiar with this technology is easy to determine.Certainly, actual amount will be according to specific prescription formulation, used specific compound, application method and medicine-feeding part, with the host that will receive treatment and disease and change.Changing pharmaceutically-active many factors must take into account, as making in year, body weight, sex, food, administration time, route of administration, drainage rate, patient's states, drug regimen, the tube ∏ of Xi houses of prostitutes or actresses in the Jin and Yuan Dynasties spinulose tree fern being taken in drug reaction

Below some embodiment just to explanation the present invention and not limiting the scope of the invention, invention scope is only limited by the claim that is attached to the application.

Among the embodiment, proton and nuclear magnetic resonance of carbon spectrum (NMR) (are used CDCl below ₃Or D ₂O makes internal standard substance) and phosphorus NMR spectrum (use 85%H ₃PO ₄The aqueous solution is made internal standard substance) on Bruker WM360 spectrograph, carry out.Infrared spectra (IR) is measured with Perkin-Elmer 1800 Fourier transform spectrometers." flash chromatography " is meant method (Still, the W.C. of Still; Kahn, M.; Mitra, A; J.Org.Chem., 1978,43,2923) carry out with E.Merck silica gel (230-400 order).Reverse-phase chromatography is used the C18(octadecylsilane that is bonded on the silica gel, 40-μ m particle diameter, J.T.Baker manufacturer under positive nitrogen pressure) carry out.

Embodiment 1

Etoposide formaldehyde glucosides 4 '-(the compound VI is a) for organic phosphate disodium salt

2.30g(3.91mmol) suspension induction stirring and the warm generation closely completely solution of Etoposide formaldehyde glucosides in the dry acetonitrile of 210ml.This solution is chilled to room temperature, adds 2.36ml(13.5mmol) N, the N-diisopropyl ethyl amine.Then, this mixture is chilled to 0 ℃ and in 30 seconds, add 666mg(4.34mmol with syringe) POCl ₃This mixture slowly rises to room temperature and continues under room temperature and stirred 63 hours in 2-3 hour.Then, shifting out the 20%(volume) content and resembling handles with diethylamine the embodiment 2.Rest part 6.0g(71.4mmol) sodium bicarbonate is in the solution-treated of 110ml deionized water (110ml), this mixture at room temperature stirred 80 minutes, then, use the 20ml saturated sodium bicarbonate aqueous solution, 125ml deionized water and 350ml ethyl acetate are distributed.Organic layer extracts with the 50ml deionized water, combining water layer and with the washing of 250ml ethyl acetate, and 0.5mm vacuum-treat 1 hour is desolvated to remove under room temperature then.The aqueous solution is partly used the pillar processing (after the methyl alcohol filling, watering balance) that 15cm is bonded to the 4cm internal diameter of the octadecylsilane on the silica gel is housed.Behind all aqueous solution part upper props, so that remove inorganic salt, use 4: 1 H then with the 175ml water elution ₂O: CH ₃The OH eluted product.Under 0.5 torr, concentrate, obtain 744mg(36%) pure title compound, be colorless solid.Or use lyophilize, and obtain pure title compound, be very loose low density solid.

IR（KBr）3426，1775，1593，1505，1486，1337，1239，1191，1122，1078，1034，983，927，888，876，851，840，697，684，664，547cm ^-1.

360 MHz ¹H NMR(D ₂O) δ 6.93(s, 1H), 6.59(s, 1H), 6.27(s, 2H), 5.93(d, 2H), 5.09(d, 1H, J=2.8Hz), 4.83(q, 1H, J=5.0Hz), 4.68(d, 1H, J=7.9Hz), 4.62(d, 1H, J=5.7Hz), 4.47-4.35(m, 2H), 4.24(dd, 1H, J=4.4 and 10.4Hz), 3.64(s, 6H), 3.68-3.52(m, 3H), 3.44-3.30(m, 3H), 3.17-3.07(m, 1H), and 1.31(d, 3H, J=5.0Hz).

90 MHz ¹³C NMR（D ₂O）δ178.5，151.8，148.1，146.1，135.0，132.6，130.9，127.4，109.9，109.5，107.4，101.3，100.4，99.6，79.2，73.7，72.7，72.2，69.1，67.1，65.4，55.6，42.8，40.3，37.5，18.8.

146 MHz ³¹P NMR（D ₂O）δ3.79.

Mass spectrum (FAB), m/e, 713(M ⁺+ H) .C ₂₉H ₃₁Na ₂O ₁₆P requires M ⁺, 712.

Analytical calculation C ₂₉H ₃₁Na ₂O ₁₆P:C, 48.89; H, 4.39; Na, 6.45.

Actual measurement ^*: C, 48.72; H, 4.56; Na, 6.56.

* use Karl Fischer assay 8.16%H ₂O is proofreaied and correct.

Embodiment 2

Etoposide formaldehyde glucosides 4 '-(two-[N, N-diethyl] phosphamide) (VII, X=O, R ¹=methyl, R ⁶=H, Y=N(C ₂H ₅) ₂, R ²=R ³=ethyl)

As embodiment 1, the 20%(volume) Etoposide formaldehyde glucosides and POCl ₃Mixture of reaction products, be added in the 4ml diethylamine and under room temperature, stirred 3 hours.Vacuum is steamed and is desolventized, and the light orange residue is purified through flash chromatography on silica gel.Methylene dichloride wash-out with containing 4% methyl alcohol obtains 271.3mg(46.9%) pure title compound, be light yellow solid.

IR（KBr）3408，2974，2936，2877，1774，1598，1508，1486，1467，1421，1383，1339，1234，1191，1162，1130，1098，1079，1037，902，858，795，713，700，544cm ^-1.

360 MHz ¹H NMR（CDCl ₃）δ6.79，（s，1H），6.50（s，1H），6.20（s，2H），5.96（ABq，2H），4.87（d，1H，J＝3.2Hz），4.71（q，1H，J＝5.1Hz），4.61（d，1H，J＝7.6Hz），4.57（d，1H，J＝5.2Hz），4.39（dd，1H，J＝9.1 and 10.2Hz），4.22-4.13（m，2H），3.74（m，1H），3.65（s，6H），3.55（m，1H），3.40（m，1H），3.32-3.10（m，11H），2.94-2.83（m，1H），1.37（d，3H，J＝5.1Hz），1.10（m，12H）.

146 MHz ³¹P NMR（CDCl ₃）δ16.49.

Mass spectrum (FAB), m/e, 779(M ⁺+ H), 573(M ⁺-sucrose) .C ₃₇H ₅₁N ₂O ₁₄P requires M ⁺, 778.

Embodiment 3

Etoposide formaldehyde glucosides 4 '-(N, N-[2-chloroethyl] phosphoryl chloride) (VII, R ¹=methyl, R ⁶=H, X=O, Y=Cl, R ²=R ³=CH ₂CH ₂Cl)

2.00g(3.40mmol) Etoposide formaldehyde glucosides under induction stirring, is warmed to nearly perfect solution in the suspension of the dry acetonitrile of 220ml.This mixture is chilled to room temperature and uses 2.05ml(11.8mmol) N, the N-diisopropyl ethyl amine is handled.Under nitrogen atmosphere, this mixture is chilled to again 0 ℃ and in 30 seconds, add 624mg(4.01mmol with syringe) phosphoryl chloride.Stirred the mixture 2.5 hours in 0 ℃ of following magnetic, under room temperature, stirred 1.5 hours again.Add 1.82(10.2mmol rapidly) two-(2-chloroethyl amine) hydrochloride, add 2.10ml(12.0mmol again) and N, the N-diisopropyl ethyl amine.Stirred this mixture 84 minutes under room temperature, vacuum concentration is dissolved in 400ml ethyl acetate and the 5ml methyl alcohol to 5ml.(2 * 200ml), the solution of water (150ml) and salt solution (150ml) washing gained is also used Na with the damping fluid of pH5 ₂SO ₄/ Mg SO ₄Dry.Solvent evaporated obtains orange/yellow solid, and this solid of dichloromethane solution wash-out with flash chromatography on silica gel and 3～4% methyl alcohol obtains 1.25g(45.4%) pure title compound, be colorless solid.

360 MHz ¹H NMR（CDCl ₃）δ6.82（s，1H），6.52（s，1H），6.27（s，2H），5.99（d，2H），4.90（d，1H，J＝3.4Hz），4.73（q，1H，J＝5.0Hz），4.65-4.60（m，2H），4.41（m，1H），4.25-4.15（m，2H），3.75-3.65（m，5H），3.72（s，6H），3.60-3.23（m，9H），2.91-2.80（m，1H），1.38（d，3H，J＝5.0Hz）.

146 MHz ³¹P NMR(CDCl ₃) δ 11.16 and 10.96(be because chirality phosphorus has two peaks).

Mass spectrum (FAB), m/e, 812,810,808.

C ₃₃H ₃₉Cl ₃NO ₁₄P requires M ⁺( ³⁵Cl) 809.

Embodiment 4

Etoposide formaldehyde glucosides 4 '-thiophosphatephosphorothioate disodium salt (compound VI b)

2.04g(3.47mmol) Etoposide formaldehyde glucosides is warmed to nearly perfect solution under the suspension induction stirring of 175ml acetonitrile.Add 2.00ml(11.5mmol after this solution is chilled to room temperature) N, the N-diisopropyl ethyl amine.Again this mixture is chilled to 0 ℃ and in 30 seconds, add 0.720g(4.17mmol with syringe) thiophosphoryl chloride.In 2～3 hours this mixture slowly being warmed to room temperature also at room temperature continues to stir 16 hours.Then, this mixture is warmed to 30～35 ℃ and under this temperature, kept 4 hours.Dichloromethane solution through TLC(50% methyl alcohol) observe, the Rf value of main new spot is than Etoposide formaldehyde glucosides height.Reaction mixture is handled with the 7.4g solid sodium bicarbonate, adds the 100ml deionized water then.This mixture stirred 1.5 hours down at 28～25 ℃, at room temperature stirred then 1.5 hours.Mixture is with the 200ml deionized water, and 30ml saturated sodium bicarbonate and 300ml ethyl acetate are distributed.Further operation and flash chromatography carry out according to the method for embodiment 1, obtain 1.03g(40.8%) pure title compound, be colorless solid.

360 MHz ¹H NMR(D ₂O) δ 6.93(s, 1H), 6.60(s, 1H), 6.27(s, 2H), 5.93(d, 2H), 5.09(d, 1H, J=2.8Hz), 4.83(q, 1H, J=5.0Hz), 4.68(d, 1H, J=7.8Hz), 4.63(d, 1H, J=5.7Hz), 4.47-4.35(m, 2H), 4.24(dd, 1H, J=4.3 and 10.5Hz), 3.64(s, 6H), 3.67-3.52(m, 3H), 3.47-3.29(m, 3H), 3.17-3.07(m, 1H), and 1.31(d, 3H, J=5.0Hz).

Mass spectrum (FAB), m/e 728(M ⁺), 706(M ⁺+ H=Na).

C ₂₉H ₃₁Na ₂O ₁₅PS requires M ⁺, 728.

Embodiment 5

Etoposide formaldehyde glucosides 4 '-[[N, two (2-chloroethyl) amino of N-]-[and the N-(3-hydroxypropyl) amino]] phosphoric acid ester (VII, X=O, R ¹=methyl, R ⁶=H, R ²=R ³=2-chloroethyl, Y=-NH(CH ₂) ₃OH)

280mg(0.346mmol) the solution magnetic of embodiment 3 compounds and 3ml methylene dichloride stirs and use 33.5mg(0.446mmol down) 3-amino-1-propyl alcohol and the processing of 1ml dichloromethane solution.After 5 minutes, add 31.0mg(0.413mmol again) solution of 3-amino-1-propyl alcohol and the absolute anhydrous methanol of 0.5ml.With 4 preparation type TLC plates (1mm, E.Merck silica gel) this reaction mixture of purifying, with the dichloromethane solution expansion of 5～8% methyl alcohol.The bands of a spectrum of the product of wanting are with the ethyl acetate solution wash-out of 5% methyl alcohol, then, vacuum-evaporation, dry under 0.1 torr again, obtain 185mg(63%) pure title compound, be colorless solid (non-enantiomer mixture of phosphorus).

360 MHz ¹H NMR(CDCl ₃) δ 7.20(br s, 1H), 6.80(s, 1H), 6.50 and 6.48(2s, 1H), 6.26 and 6.25(2s, 2H), 5.97(d, 2H), 4.88(m, 1H), 4.73(q, 1H), 4.64-4.57(m, 2H), 4.40(m, 1H), 4.21-4.13(m, 2H), 3.71,3.70(2s, 6H), 3.71-3.06(m, 18H), 2.90-2.80(m, 1H), 1.37(d, 3H).

Mass spectrum (FAB), m/e, 849,851(M ⁺+ H, ³⁵Cl, ³⁷Cl) .C ₃₆H ₄₇Cl ₂N ₂O ₁₅P requires M ⁺848( ³⁵Cl) and 850( ³⁷Cl).

Embodiment 6

Etoposide formaldehyde glucosides 4 '-[[N, two (2-chloroethyl) amino of N-]-[and N-[(3-nitropyridine-2-yl) two sulphur] ethyl] amino] phosphoric acid ester (VII, X=O, R ¹=methyl, R ⁶=H, R ²=R ³=2-chloroethyl, Y=-NH(CH ₂) ₂-SS-(3-nitropyridine-2-yl)

248mg(0.306mmol) embodiment 3 compounds and 105mg(0.393mmol) 2-(3-nitropyridine base)-the 1-(2-amino-ethyl) mixture of disulphide hydrochloride handles with the 7ml methylene dichloride, adds 100 μ l(0.570mmol again) diisopropyl ethyl amine and the dry methyl alcohol of 0.5ml.Gained solution stirred under room temperature 1.5 hours, then, directly purified with 4 preparation type TLC plates (1mm, E.Merck silica gel), with the ethyl acetate solution expansion of 4-5% methyl alcohol.Obtain requiring the elutriant of product bands of a spectrum with the ethyl acetate solution wash-out of 5% methyl alcohol, vacuum-evaporation, dry under 0.1 torr then, obtain 231.7mg(75.3%) pure title compound, be Huang-brown solid (non-enantiomer mixture of phosphorus).

IR（KBr）1774，1598，1584，1559，1509，1486，1456，1421，1397，1342，1236，1160，1128，1096，1038，1004，926，857，747，699cm ^-1.

360 MHz ¹H NMR(CDCl ₃) δ 8.81 and 8.77(2m, 1H), 8.48(m, 1H), 7.33(m, 1H), 6.81(s, 1H), 6.51 and 6.50(2s, 1H), 6.26(br s, 2H), 5.97(d, 2H), 4.89(m, 1H), 4.73(q, 1H), 4.65-4.52(m, 3H), 4.41(m, 1H), 4.24-4.14(m, 2H), 3.71,3.70(2s, 6H), 3.71-2.85(m, 19H), 2.68(br s, 1H, OH), 2.37(br s, 1H, OH), 1.37(d, 3H).

Mass mass spectrum (FAB), m/e, 1005,1007(M ⁺+ H, ³⁵Cl, ³⁷Cl) .C ₄₀H ₄₇Cl ₂N ₄O ₁₆PS ₂Require M ⁺, 1004( ³⁵Cl) and 1006( ³⁷Cl).

Embodiment 7

Etoposide formaldehyde glucosides 4 '-diphenyl phosphoester (R '=methyl, R ⁶=H, R ⁷=R ⁸=phenyl)

10.50g(17.84mmol) Etoposide formaldehyde glucosides is (at 80 ℃/0.5 torr pressure Long  Cha ₂O ₅The dry mistake) suspension in the dry acetonitrile of 450ml, magnetic stirs use 4.20ml(24.1mmol down) the diisopropyl ethyl amine processing, then, add 2.00ml(9.65mmol with syringe) diphenyl phosphate chloride.Under nitrogen atmosphere, stirred the mixture the whole solvolysises of Etoposide formaldehyde glucosides 2 hours in 50 ℃.Add 1.80ml(8.68mmol again) diphenyl phosphate chloride and kept 72 hours in 45 ℃.Add 0.75ml(4.3mmol in addition) diisopropyl ethyl amine and 0.80ml(3.86mmol) behind the diphenyl phosphate chloride, this mixture was in 40～45 ℃ of restir 72 hours.Use 0.40ml(1.93mmol again) diphenyl phosphate chloride handles and kept 22 hours down in 40～45 ℃.Add the 20ml Virahol, vacuum-evaporation is dissolved in solid residue in the 500ml methylene dichloride and uses the 400ml water dispenser.Water layer 100ml dichloromethane extraction merges organic layer, with the water washing of 250ml salt, sodium sulfate/dried over mgso.Do flash chromatography on silica gel with the methylene dichloride of 2-3% methyl alcohol behind the rotary evaporation, obtain 12.50g(85%) pure title compound, be colorless solid.

FAB MS m/e(relative density) 820(M+H) ⁺.

IR（KBr）3460，2925，1775，1601，1490cm ^-1.

¹H NMR（CDCl ₃）δ7.28（m，8H），7.15（m，2H），6.78（s，1H），6.47（s，1H），5.95（m，2H），4.85（d，J＝3.5Hz，1H），4.71（m，1H），4.60（d，J＝7.6Hz，1H），4.56（d，J＝5.1Hz，1H），4.38（m，1H），4.22-4.13（m，2H），3.72-3.60（m，1H），3.48（s，6H），3.54-3.28（m，3H），3.23（dd，J＝14.2，5.3Hz，1H），2.78m，1H），1.35（d，J＝5.1Hz，3H）.

Analysis requires C ₄₁H ₄₁O ₁₆P:C, 60.00; H, 5.04. surveys C, 60.20; H, 5.16.

Embodiment 8

Etoposide formaldehyde glucosides 4 '-phosphoric acid ester (V; R ¹=CH ₃; R ⁶=H, R ⁷=R ⁸=H)

With the 0.198g(0.87mmol that takes out in the new uncork) platinum oxide (Aldrich chemical company product) is added to 0.79g(0.962mmol) the Etoposide formaldehyde glucosides 4 of embodiment 7 preparations '-solution of diphenyl phosphate and the absolute dehydrated alcohol of 95ml in.Under room temperature and 45～50PS1 pressure in the Parr hydrogenator this solution of hydrogenation 4 hours.Through the Celite pad filter reaction mixture and use ethanol elution.Vacuum concentration was also used five phosphorus oxide dry 14 hours in a vacuum, obtained required product 0.627g(94%), be white solid.

FAB MS m/e(relative density) 669(M+H) ⁺

IR（KBr）3440，2930，1778，1604，1498cm ^-1.

¹H NMR（DMSO-d ₆）δ6.93（s，1H），6.46（s，1H），6.12（s，2H），5.94（m，2H），5.17（bs，1H），4.86（d，J＝3.93Hz，1H），4.64（q，J＝7.5，5.8Hz，1H），4.51-4.42（m，2H），4.20（d，J＝10.7Hz，1H），4.01（dd，J＝12.1，5.3Hz，1H），3.51（s，6H），3.51-2.75（m，7H），2.83（m，1H），1.16（d，J＝5.1Hz，3H）.

¹³C NMR（DMSO-d ₆）δ174.5，151.2，151.1，147.7，146.2，126.1，132.3，128.8，109.8，109.7，107.9，101.5，101.2，98.5，80.0，74.3，72.7，71.7，67.6，67.2，65.7，55.8，43.0，37.1，20.2，18.5.

Analytical calculation C ₂₉H ₃₃O ₁₆P.0.85%H ₂O:C, 50.95; H, 5.11. surveys C, 51.42; H, 4.97.

Embodiment 9

Etoposide formaldehyde glucosides 4 '-two (2,2,2-three chloroethyls) phosphoric acid ester (VII; R ¹=methyl, R ⁶=H, R ⁷=R ⁸=CH ₂CCl ₃)

Repeat embodiment 7 described processes with two (2,2,2-three chloroethyls) chlorine phosphoric acid ester, obtain the title compound of 100% productive rate, after doing flash chromatography on the silica gel, be colorless solid.

IR（KBr）1780，1610，1490，1415，1345，1240，1040，960，725cm ^-1.

300 MHz ¹H NMR（CDCl ₃）δ6.81（s，1H），6.49（s，1H），6.27（s，2H），5.98（dd，2H），4.88（d，1H，J＝3.4Hz），4.82-4.70（m，5H），4.64（d，1H，J＝7.6Hz），4.61（d，1H，J＝5.3Hz），4.41（dd，1H），4.25-4.13（m?H），3.75（m，1H），3.73（s，6H），3.56（m，1H），3.43（dd，1H），3.34-3.24（m，3H），2.91-2.82（m，1H），1.38（d，3H，J＝4.9Hz）.

Mass spectrum (FAB), m/e=928.9848(M ⁺+ H).

C ₃₃H ₃₆Cl ₆O ₁₆P requires 928.9872.

Embodiment 10

From Etoposide formaldehyde glucosides 4 '-phosphoric acid ester prepare Etoposide formaldehyde glucosides 4 '-organic phosphate disodium salt

Method A

20g commodity Dowex 50 * 8～100 hydrogen type cation exchange resins (Aldrich chemical company product) are with excessive 1N sodium-hydroxide treatment.With pack into 2cm post and of gained sodium type resin with water balance.With 1.25g(1.87mmol) Etoposide formaldehyde glucosides 4 '-phosphoric acid ester (embodiment 8 preparation) is dissolved in the 25ml deionized water and from capital and adds exchange column, water wash-out.Collection contains the flow point of title compound, filters, and freeze-drying gets the 1.15g title compound, is white bulk materials.

Method B

With 50ml deionized water and 3.00g(35.7mmol) sodium bicarbonate is added to 2.90g(4.34mmol) crude product Etoposide formaldehyde glucosides 4 '-phosphoric acid ester (embodiment 8 preparations) in.At room temperature stirred this mixture 30 minutes, at this moment dioxo carbon stops to discharge.Then, as described in embodiment 1, do chromatogram.Earlier use 4: 1 water/methanol-eluted fractions again, obtain 1.90g(61% with the 300ml deionized water) pure title compound is loose white solid after the freeze-drying.

Embodiment 11

Repeat embodiment 2 described logical methods, but used diethylamine replaces with following listed amine, obtain corresponding Etoposide formaldehyde glucosides 4 '-the di(2-ethylhexyl)phosphate carboxylic acid amide esters.

The amine compound VII

(X=O, R ¹=methyl, R ⁶=H, Y=NR ²R ³)

R ²R ³

- -

Propylamine H CH ₂CH ₂CH ₃

Thanomin H CH ₂CH ₂OH

Methoxyethyl amine H CH ₂CH ₂OCH ₃

N-acetylethylenediamine H CH ₂CH ₂NC(O) CH ₃

2-methacrylic amine H CH ₂CH(CH ₃)=CH ₂

Allyl amine H CH ₂CH=CH ₂

Dimethylaminopropylamine H (CH ₂) N(CH ₃) ₂

N-methyl ethylenediamine H CH ₂CH ₂NCH ₃

Trifluoro ethamine H CH ₂CF ₃

2-aminoothyl mercaptan H CH ₂CH ₂SH

Hexahydroaniline H cyclohexyl

2-amino-1-methoxyl group H CH(CH ₃) CH ₂OCH ₃

Propane

The 2-(ethylmercapto group)-ethamine H CH ₂CH ₂SCH ₂CH ₃

Chlorethamin H CH ₂CH ₂Cl

4-Trans-4-Amino Cyclohexanol H

Ethylmethylamine CH ₃CH ₂CH ₃

N-Ethylbutylamine CH ₂CH ₃(CH ₂) ₃CH ₃

Methylethylolamine CH ₃CH ₂CH ₂O

Two (2-chloroethyl) amine CH ₂CH ₂Cl CH ₂CH ₂Cl

The 2-third monoethanolamine CH ₂CH ₂CH ₃CH ₂CH ₂OH

3-methylamino-propionitrile CH ₃CH ₂CH ₂CN

Piperidines R ²+ R ³=-(CH ₂) ₅-

Embodiment 12

Repeat embodiment 3 described logical methods, but used two (2-chloroethyl) amine replace with following listed amine, obtain corresponding Etoposide formaldehyde glucosides chlorine phosphoramidate.

The amine compound VII

(X=O, R ¹=methyl, R ⁶=H, Y=Cl)

R ²R ³

- -

Propylamine H CH ₂CH ₂CH ₃

Thanomin H CH ₂CH ₂OH

Methoxyethyl amine H CH ₂CH ₂OCH ₃

N-acetylethylenediamine H CH ₂CHNC(O) CH ₃

2-methacrylic amine H CH ₂CH(CH ₃)=CH ₂

Allyl amine H CH ₂CH=CH ₂

Dimethylaminopropylamine H (CH ₂) ₃N(CH ₃) ₂

N-methyl ethylenediamine H CH ₂CH ₂NCH ₃

Trifluoro ethamine H CH ₂CF ₃

2-aminoothyl mercaptan H CH ₂CH ₂SH

Hexahydroaniline H cyclohexyl

2-amino-1-methoxyl group H CH(CH ₃) CH ₂OCH ₃

Propane

The 2-(ethylmercapto group)-ethamine H CH ₂CH ₂SCH ₂CH ₃

Chlorethamin H CH ₂CH ₂Cl

4-Trans-4-Amino Cyclohexanol H 4-hydroxy-cyclohexyl

Ethylmethylamine CH ₃CH ₂CH ₃

N-Ethylbutylamine CH ₂CH ₃(CH ₂) ₃CH ₃

Methylethylolamine CH ₃CH ₂CH ₂OH

Diethylamine CH ₂CH ₃CH ₂CH ₃

The 2-third monoethanolamine CH ₂CH ₂CH ₃CH ₂CH ₂OH

3-methylamino-propionitrile CH ₃CH ₂CH ₂CN

Piperidines R ²+ R ³=-(CH ₂) ₅-

Embodiment 13

Repeat embodiment 5 described logical methods, but used 3-aminopropanol obtains corresponding asymmetric Etoposide formaldehyde glucosides phosphoryl diamine ester with following amine replacement.

The amine compound VII

(X=O, R ¹=methyl, R ⁶=H, Y=NR ⁴R ⁵,

R ²＝R ³＝CH ₂CH ₂Cl

R ⁴R ⁵

- -

Propylamine H CH ₂CH ₂CH ₃

Thanomin H CH ₂CH ₂OH

Methoxyethyl amine H CH ₂CH ₂OCH ₃

N-acetylethylenediamine H CH ₂CHNC(O) CH ₃

2-methacrylic amine H CH ₂CH(CH ₃)=CH ₂

Allyl amine H CH ₂CH=CH ₂

Dimethylaminopropylamine H (CH ₂) N(CH ₃) ₂

N-methyl ethylenediamine H CH ₂CH ₂NCH ₃

Trifluoro ethamine H CH ₂CF ₃

2-aminoothyl mercaptan H CH ₂CH ₂SH

Hexahydroaniline H cyclohexyl

2-amino-1-methoxyl group H CH(CH ₃) CH ₂OCH ₃

Propane

The 2-(ethylmercapto group)-ethamine H CH ₂CH ₂SCH ₂CH ₃

Chlorethamin H CH ₂CH ₂Cl

4-Trans-4-Amino Cyclohexanol H 4-hydroxy-cyclohexyl

Ethylmethylamine CH ₃CH ₂CH ₃

N-Ethylbutylamine CH ₂CH ₃(CH ₂) ₃CH ₃

Methylethylolamine CH ₃CH ₂CH ₂OH

Two (2-chloroethyl) amine CH ₂CH ₂Cl CH ₂CH ₂Cl

The 2-third monoethanolamine CH ₂CH ₂CH ₃CH ₂CH ₂OH

3-methylamino-propionitrile CH ₃CH ₂CH ₂CN

Piperidines R ²+ R ³=-(CH ₂) ₅-

Embodiment 14

Repeat the logical method of embodiment 7, but used diphenyl phosphate chloride replaces with following listed chlorine phosphoric acid ester, obtain corresponding Etoposide formaldehyde glucosides 4 '-phosphodiester (X=O, R ¹=methyl, R ⁶=H, R ⁷=R ⁸=following R).

The chlorine phosphoric acid ester [(RO) ₂P(O) Cl]

The R=methyl

Ethyl

Benzyl

Right-nitrobenzyl

Right-nitrophenyl

Right-bromobenzyl

Right-the oil of mirbane ethyl

Cyanoethyl

Neighbour-(tertiary butyl) phenyl

Embodiment 15

Repeat embodiment 1～16 described logical method, but used Etoposide formaldehyde glucosides raw material replaces with corresponding Etoposide thiophene aldehyde glycoside compounds, obtain corresponding Etoposide thiophene aldehyde glucosides product.

Claims (30)

1, the preparation method of general formula (V) compound or its pharmacy acceptable salt,

R in the general formula ⁶Be H; R ¹Be selected from (C _1-10) alkyl, (C _2-10) thiazolinyl, (C _5-6) cycloalkyl, 2-furyl, 2-thienyl, (C _6-10) aryl, (C _7-14) aralkyl and (C _8-14) arylalkenyl, wherein each aromatic ring can not or have one or more to be selected from fontanel element (C _1-8) alkyl, (C _1-8) alkoxyl group, hydroxyl, nitro and amino substituting group; Or R ¹And R ⁶(C respectively does for oneself _1-8) alkyl; Or R ¹And R ⁶Form (C with the carbon that links to each other _5-6) cycloalkyl; X is oxygen or sulphur; R ⁷And R ⁸Be selected from H separately, (C _1-5) alkyl, A-replaces (C _1-5) alkyl, (C _3-6) cycloalkyl, A-replaces (C _3-6) cycloalkyl, (C _6-10) aryl, A-substituted aryl, the aryl that alkyl replaces, (C _7-14) aralkyl, the aralkyl that A-substituted aralkyl and alkyl replace, it is to be selected from hydroxyl that wherein said A-replaces; alkoxyl group, alkane carbonyl oxygen base, cyano group; amino, alkylamino, dialkylamino; carboxyl, alkylthio, sulfydryl; the sulfydryl sulfenyl, nitropyridine base disulfide base, alkyl amido; alkyloyl, formamyl, one or more groups of nitro and fontanel element.

This method may further comprise the steps:

(a) general formula (1) compound and general formula P (x) Cl ₃Compound reacts the intermediate that forms general formula (2) in the presence of the hydrogen receptor;

R in the general formula ¹, R ⁶With the definition of X the same and

(b) randomly in the presence of alkali, hydrolysis general formula (2) compound becomes general formula (3) compound or its pharmacy acceptable salt, or

(c) compound of general formula (2) and at least one normal ROH and ROH react, wherein R ⁷And R ⁸Definition the same, condition is R ⁷And R ⁸Not hydrogen and reaction in the presence of the hydrogen receptor; And R ⁷And R ⁸One of be hydrogen, can randomly transform this compound through alkaline purification is pharmacy acceptable salt.

2, according to the method for claim 1, prepare following compound or its pharmaceutically acceptable salt of general formula,

R in the formula ¹, R ⁶With the definition of X with claim 1.

3, the process of claim 1 wherein R ⁶Be H and R ¹Be methyl or 2-thienyl.

4, the method for claim 2, wherein R ⁶Be H and R ¹Be methyl or 2-thienyl.

5, the method for claim 2, wherein R ⁶Be H and R ¹It is methyl.

6, the method for claim 5, wherein X is an oxygen.

7, the method for claim 5, wherein X is a sulphur.

8, the process of claim 1 wherein that pharmacy acceptable salt is a sodium salt.

9, with the method for claim 1 prepare Etoposide formaldehyde glucosides 4 '-disodic alkaliine.

10, with the method for claim 1 prepare Etoposide formaldehyde glucosides 4 '-the thiophosphoric acid disodium salt.

11, the process of claim 1 wherein R ⁷Be selected from (C _1-5) alkyl, (the C that A-replaces _1-5) alkyl, (C _3-6) cycloalkyl, (the C that A-replaces _3-6) cycloalkyl, (C _6-10) aryl, the aryl that A-replaces, the aryl that alkyl replaces, (C _1-14) aralkyl, the aralkyl that aralkyl that A-replaces and alkyl replace, R ⁸Be H or R ⁷Defined certain group, the definition of substituent A is the same.

12, the method for claim 11, wherein R ⁶Be H and R ¹Be methyl or 2-thienyl.

13, the method for claim 12, wherein R ⁷And R ⁸Be selected from (C separately _1-5) alkyl, fontanel generation (C _1-5) alkyl, (the C that cyanogen replaces _1-5) alkyl, (C _6-10) aryl and (C _7-14) aralkyl, the aromatic ring of wherein said aryl or civilian alkyl is substituted with arbitrarily and is selected from alkyl, the group of fontanel element and nitro.

14, the method for claim 13, wherein R ¹It is methyl.

15, the method for claim 14, wherein X is an oxygen.

16, the method for claim 15, wherein R ⁷And R ⁸The phenyl of respectively doing for oneself.

17, the method for claim 15, wherein R ⁷And R ⁸Respectively do for oneself 2,2,2-three chloroethyls.

18, the following compound of general formula or the preparation method of its pharmacy acceptable salt,

R in the formula ¹, R ⁶The same with the definition of X; Y is Cl, OH or NR ⁴R ⁵; R ², R ³, R ⁴And R ⁵Be selected from H separately, (C _1-5) alkyl, (C _2-5) thiazolinyl, (C _3-6) cycloalkyl, (the C that A-replaces _1-5) alkyl, (the C that A-replaces _3-5) thiazolinyl, (the C that A-replaces _3-6) cycloalkyl; Or R ², R ³Form 3-6 unit ring together with the nitrogen that links to each other; Or R ⁴, R ⁵Form 3-6 unit ring together with the nitrogen that links to each other; Wherein said A-substituent definition is the same,

This method comprises the steps:

(a) intermediate of mantoquita (2) and general formula are HNR ²R ³Amine reaction generate the compound of general formula (4).

R wherein ²And R ³Definition the same; With

(b) compound of general formula (4) is HNR with second kind of general formula randomly ⁴R ⁵Amine or its acid addition salt reaction generate the compound that reactant salt generates general formula (5),

R wherein ⁴And R ⁵Definition the same, or

(c) hydrolysis compound (4) on alkali exists randomly generates general formula (6) compound or its pharmacy acceptable salt.

19, the method for claim 18, wherein R ⁶Be H; R ¹Be methyl or 2-thienyl; Y is Cl or NR ⁴R ⁵; X is oxygen or sulphur, R ², R ³, R ⁴And R ⁵Be selected from H separately, (C _1-5) alkyl, fontanel generation (C _1-5) alkyl, (the C that hydroxyl replaces _1-5) (the C that replaces of alkyl and nitropyridine base two sulphur silicon _1-5) alkyl.

20, the method for claim 19, wherein X is an oxygen.

21, the method for claim 20, wherein R ¹It is methyl.

22, the method for claim 21, wherein R ²And R ³The 2-chloroethyl of respectively doing for oneself, Y is Cl.

23, the method for claim 21, wherein Y is NR ⁴R ⁵

24, the method for claim 23, wherein R ², R ³, R ⁴And R ⁵The ethyl of respectively doing for oneself.

25, the method for claim 23, wherein R ²And R ³The 2-chloroethyl of respectively doing for oneself, R ⁴Be H, R ⁵It is the 3-hydroxypropyl.

26, the method for claim 23, wherein R ²And R ³The 2-chloroethyl of respectively doing for oneself, R ⁴Be H, R ⁵Be

27, a kind of pharmaceutical composition, said composition contain the claim 1 of antitumor significant quantity or the compound and the pharmaceutically acceptable carrier of 18 preparations.

28, the pharmaceutical composition of claim 27, wherein said compound be Etoposide formaldehyde glucosides 4 '-organic phosphate disodium salt.

29, a kind of method that suppresses mammal tumor, this method comprise to tumor host with the claim 1 of effective antitumor amount or the compound of 18 preparations.

30, the method for claim 29, wherein said compound be Etoposide thiophene aldehyde glucosides 4 '-organic phosphate disodium salt.