CN1092654C - 4-phenylpiperidine compound - Google Patents

4-phenylpiperidine compound Download PDF

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CN1092654C
CN1092654C CN97182237A CN97182237A CN1092654C CN 1092654 C CN1092654 C CN 1092654C CN 97182237 A CN97182237 A CN 97182237A CN 97182237 A CN97182237 A CN 97182237A CN 1092654 C CN1092654 C CN 1092654C
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acid
alkyl
described compound
paroxetine
compound
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CN1256692A (en
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F·B·G·贝恩克
F·范达仁
J·M·莱蒙斯
T·H·A·彼得
F·皮查
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Synthon BV
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Abstract

The present invention relates to a compound shown in a formula (I) and medical salt thereof, and the formula (I) is disclosed in the specification, wherein R stands for alkyl or alkynyl which contains 1 to 4 carbon atoms, or phenyl optionally substituted by C1 to 4 alkyl, alkyl sulphide radical, alkoxy, halogen, nitro, acylamino, methylsulfonyl and methylene dioxy, or stands for tetralyl, R<1> stands for hydrogen, trifluoro (C1 to 4) alkyl, alkyl or alkynyl, X stands for hydrogen, alkyl which contains 1 to 4 carbon atoms, alkoxy, trifluoroalkyl, hydroxyl, halogen, methylthio or aralkoxy, and R<2> stands for C1 to C10 alkyl, or phenyl optionally substituted by one of the following groups or a plurality of the following groups: C1 to C10 alkyl, halogen, nitro, hydroxyl and/or alkoxy.

Description

The 4-phenylpiperidine compound
The present invention relates to three to replace 4-phenylpiperidine compounds, its preparation method, contained the medicine of these compounds, and the application in making medicine of this compounds.
The compound paroxetine that is shown below, trans-4-(4 '-fluorophenyl)-3-(3 ', 4 '-methylenedioxy benzene oxygen ylmethyl) piperidines is a known compound, and has been used in already in the medicine of treatment dysthymia disorders.
Figure C9718223700051
Paroxetine be with the salifiable form of pharmaceutically acceptable acid shape as therapeutical agent.What clinical trial was first adopted is acetate.
A kind of known salts of paroxetine is a hydrochloride.This salt is considered active substance in some kinds of marketed drugs products such as Paxil or Seroxat.The Tagonis of various ways is disclosed so far:
The anhydrous form of-several crystal modifications (PCT applies for WO 96/24595);
-hydrated form, a kind of semihydrate (EP 223403) and solvation form.
At international journal of Practical Pharmacy (Intl.Journal of Pharmaceutics), 42, the comparison of the characteristic of the anhydrous form of Tagonis and paroxetine hydrated form has been described among the 135-143 (1988).
EP 223403 discloses the semihydrate and the pharmaceutical composition thereof of Tagonis.
The physics-chem characteristic of many known paroxetine salt is not suitable for operating safely and effectively and making final formulation in its manufacturing processed, this is owing to their instabilities (acetate, maleate), and has unsuitable water absorbability.
In addition, the general yield of paroxetine salt that forms by crystallization in water or non-aqueous solvent is lower, and trouble be they usually contain uncertain and unpredictable amount, be difficult to slough in conjunction with solvent.
Crystallization paroxetine hydrochloride hemihydrate compound is close to and addresses the above problem, but claims according to WO95/16448, and its limited light stability causes unnecessary painted in typical wet method pressed disc method.
And crystallization paroxetine hydrochloride hemihydrate compound only shows limited solubleness in water.
Generally believe that so far water-soluble low, as less than 3mg/ml, the dissolution rate of vivo medicine-feeding will play the speed limit effect in the absorption process.Under the paroxetine semihydrate room temperature water-soluble surpasses this threshold value with less amount.
An object of the present invention is to provide a kind of compound that improves characteristic that has.
First aspect the present invention relates to a kind of compound shown by formula I and pharmacologically acceptable salt thereof: -R representative contains the alkyl or the alkynyl of 1-4 carbon atom, or by C 1-4The optional phenyl that replaces of alkyl, alkylthio, alkoxyl group, halogen, nitro, amido, methyl sulphonyl or methylene-dioxy, or represent tetralyl;-R 1Represent hydrogen, trifluoro (C 1-4) alkyl, alkyl or alkynyl;-X represents hydrogen, contains the alkyl of 1-4 carbon atom, alkoxyl group, trifluoroalkyl, hydroxyl, halogen, methylthio group or aralkoxy;-R 2Representative
-C1-C10 alkyl,
-by the optional phenyl that replaces of or several following groups:
-C1-C10 alkyl,
-halogen,
-nitro,
-hydroxyl,
-and/or alkoxyl group.
The inventor finds that these compounds have satisfactory stability and high solubleness.Consequent superiority is that compound can reach higher concentration in smaller volume.
Preferred R group is 3 shown in the following formula, 4-methylenedioxyphenyl base:
Figure C9718223700071
Preferred X group is the fluorine that is connected on 4 of the phenyl ring.
Preferred R 2Group is represented the C1-C4 alkyl, and R most preferably 2Represent the C1-C2 alkyl, so that solubleness the best.
Under about 20 ℃, the solubleness of described compound is at least about 10mg/ml water, and the preferred dissolution degree is at least 100mg/ml water, 500mg/ml water for example, and most preferably be at least 1000mg/ml water.
According to a second aspect of the invention, provide a kind of method for preparing above-claimed cpd, the step of this method comprises: will be suc as formula 4-Phenylpiperidine compound, its salt and/or alkali and the general formula R shown in the II 2-SO 3The sulfonic acid that H represents mixes, and forms a solution, isolates the compound of solution formation thus subsequently, formula II:
Figure C9718223700072
Wherein :-R representative contains the alkyl or the alkynyl of 1-4 carbon atom, or by C 1-4The optional phenyl that replaces of alkyl, alkylthio, alkoxyl group, halogen, nitro, amido, methylsulfonyl or methylene-dioxy, or represent tetralyl;-R 1Represent hydrogen, trifluoro (C 1-4) alkyl, alkyl or alkynyl;-X represents hydrogen, contains the alkyl of 1-4 carbon atom, alkoxyl group, trifluoroalkyl, hydroxyl, halogen, methylthio group or aralkoxy; At general formula R 2-SO 3Among the H-R 2Representative
-C1-C10 alkyl,
-by the optional phenyl that replaces of or several following groups:
-C1-C10 alkyl,
-halogen,
-nitro,
-hydroxyl,
-and/or alkoxyl group.
Can be in appropriate solvent, with the free alkali of 4-Phenylpiperidine shown in the formula II, preferred paroxetine forms required acid salt solution with sulfonic acid processing as defined above, is settled out this salt subsequently in solution, thereby makes compound of the present invention.
The reaction formula of paroxetine free alkali and sulfonic compound is as follows:
Figure C9718223700081
Preferably to the temperature of solvent boiling point, form solution at about 0 ℃.
Can be randomly with gac, silica gel, diatomite or other suitable material processing solution to be purified.
And, can generate salts solution of the present invention with the organic sulfonic acid dissolving by salt with 4-Phenylpiperidine shown in the formula II.
For example, corresponding organic sulfonic acid can be joined in the solution of C1-C5 carboxylate salt (as acetate) of paroxetine and make compound of the present invention, as follows:
Figure C9718223700082
According to a third aspect of the invention we, provide the compound that obtains by aforesaid method.
According to a forth aspect of the invention, provide the application of above-claimed cpd as medicine; A fifth aspect of the present invention has related to a kind of medicine that contains this compound, and the application in the dysthymia disorders that anxiety causes before treating dysthymia disorders, obsessional idea and behavior disorder disease, Phobias, Bulimia nerovsa, apocleisis, pain, obesity, senile dementia, migraine, anorexia, social phobia, passing through.
According to a sixth aspect of the invention, provide The compounds of this invention purposes as reagent in further synthetic.Particularly, compound of the present invention can be used as initial reagent further with suitable reagent, promptly corresponding acid-respons generates further acid salt, for example generates the acid salt of paroxetine.For example, form the maleate of paroxetine with following reaction formula according to the present invention:
Figure C9718223700091
With, generate the acetate of paroxetine according to following formula:
Figure C9718223700092
This is a favourable reaction scheme, and as initial reactant, when preparing next step salt, the salt of generation has high purity owing to the sulfonate of the present invention that has adopted substantially pure for it.The inventor has demonstrated these salt and has had wonderful high purity.
Equally, compound of the present invention can with alkali such as the reaction of inorganic and/or organic bases, generate the free alkali of (disengaging) respective compound.With the paroxetine is example, and reaction is carried out according to following formula:
Compare with the free alkali for preparing according to ordinary method, the free alkali that discharges from The compounds of this invention unexpectedly has higher purity, and this is particularly important in the situation of making medicine with it.
Therefore, the new compound that the present invention at first provides can also with corresponding co-reactant, promptly contact and form hydrate and/or solvate with water and/or with solvent phase.The example of further salt, hydrate and the solvate of paroxetine is: hydrochloride oxalate dihydrate hydrobromate succinate trihydrate hydriodate tartrate hexahydrate acetate Citrate trianion methylate propionic salt embonate ethylate maleate semihydrate fumarate hydrate
The inventor proves that above-mentioned salt has wonderful high purity.
The alkali that is applicable to the preparation free alkali can be for example: sodium hydroxide, potassium hydroxide, calcium hydroxide, ammonium hydroxide, yellow soda ash, methylamine, dimethylamine, triethylamine, pyridine etc.
Because compound of the present invention shows very high solubleness, so, these compounds can come administration by the solution of for example injecting high density, small volume, and this medication is particularly advantageous for some sufferer such as manic-depressive illness patient (promptly can't or being unwilling to swallow the sufferer of medicine).
Compound of the present invention the different types of drugs composition be can be mixed with and human body and animal are used for the treatment of.Pharmaceutical composition of the present invention can only contain The compounds of this invention, or contains the The compounds of this invention that share with pharmaceutically acceptable carrier or thinner.Preferred formulation is the formulation (tablet, capsule) of those oral administration administrations, but the preparation of parenterai administration or topical also belongs to protection scope of the present invention.The highly water-soluble of The compounds of this invention has guaranteed to have high-dissolution based on the solid dosage of The compounds of this invention in the release in vitro process, and has also guaranteed after the oral administration administration good biological availability in vivo.
When preparation contains the tablet of The compounds of this invention, can there be moisture to have (for example wet granulation process) in the compressing tablet operation, also can be anhydrous compressing tablet (direct compression process, dry granulation method), and can utilize suitable coating way to carry out dressing.
Now, the present invention describes with the following example and result.Test
The crystal seed of POT.mes is prepared as follows:
2.7g (8.2mmol) paroxetine is dissolved in the 15ml hot ethanol.Adding 15ml contains the ethanol of 1.0g (10.4mmol) methylsulfonic acid, and this mixture is cooled to room temperature.When mixture reaches room temperature, mixture is placed in-20 ℃ the refrigerator and spends the night.Do not obtain the crystalline form compound.
This mixture is evaporated to dried, residual down oily matter.
It was at room temperature placed 1 month, obtain waxy solid.Take out this solid of a part and remainder is dissolved in the 10ml ethyl acetate.Add the crystallization of wax shape and this mixture is placed in-20 ℃ the refrigerator and spend the night.Be settled out white crystals.Filter and vacuum-drying.
Obtain 2.5g (5.9mmol) POT.mes.
Yield 72%.
Subsequently this crystal seed is used for following embodiment 1 and 3.
Embodiment
Embodiment 1 prepares POT.mes by paroxetine
In the 150ml boiling ethyl acetate solution that contains 43.5g (132mmol) paroxetine (according to the preparation of US 4007196 disclosed methods), add 12.7g (132mmol) methylsulfonic acid.This mixture was at room temperature placed 2 hours.Adding crystal seed subsequently also spends the night the placement under-20 ℃ of this mixture.Wash with the gained solid filtering and with the 50ml ether.The white solid vacuum-drying that generates is spent the night.Obtain 47.1g (111mol) product.
Yield 99.5%.
List the analytical characteristic that obtains by this compound in the table 1.The purity of this compound is 98% (HPLC).
Embodiment 2 prepares the paroxetine benzene sulfonate by paroxetine
3.8g (11.5mmol) paroxetine is dissolved in the 10ml hot ethyl acetate.Add 1.82g (11.5mmol) dry-out benzene sulfonic acid.Mixture was at room temperature placed 2 hours.Mixture is evaporated to dry doubling and is dissolved in the methylene dichloride, be evaporated to driedly again, obtain oily matter.
Through high vacuum (0.1mmHg) evaporation this oily matter is solidified, obtain 5.0g (1.3mmol) white-yellowish solid.In this solid, add 5ml acetone and, obtain white suspension during this period this suspension stirring 5 minutes.Filter out solid and vacuum-drying.
Obtain 4.8g (9.9mmol) product.
Yield 85%.
List the analytical characteristic that obtains by this compound in the table 1.The purity of this compound is 99.4% (HPLC).
Embodiment 3 prepares the paroxetine tosilate from paroxetine
5.0g (15mmol) paroxetine is dissolved in the 25ml hot ethyl acetate.Add 2.9g (15mmol) right-toluenesulphonic acids.Mixture is at room temperature placed 2 hours, and then in mixture, add crystal seed and in refrigerator, placed 14 hours.Leach solid and use the washing of 10ml normal hexane once.The vacuum-drying of gained white solid is spent the night.
Obtain 4.8g (10mmol) product.
Yield 67%.
List the analytical characteristic that obtains by this compound in the table 1.The purity of this compound is 99.4% (HPLC).
Embodiment 4 from paroxetine prepare paroxetine right-closilate
1.1g (3.3mmol) paroxetine is dissolved in the 3ml hot ethyl acetate.Add 90% pair-chlorobenzenesulfonic acid of 0.76g (3.3mmol).The 5ml water washing was at room temperature placed 1 hour and used to mixture.Use the dried over sodium sulfate organic layer, filter and be evaporated to dried, obtain 1.5g (2.9mmol) yellow-white product.
Yield 88%.
List the analytical characteristic that obtains by this compound in the table 1.The purity of this compound is 99.4% (HPLC).
Embodiment 5 prepares paroxetine maleate from POT.mes
1.0g (2.4mmol) POT.mes is dissolved in the 5ml hot water.In this solution, add 0.32g (2.8mmol) toxilic acid.Mixture placement under 4 ℃ is spent the night, and after this bottom settlings at flask goes out solid and yellow oil.Filter out solid/oil, with 10ml ether washing 3 times, vacuum-drying.Obtain the crystallization of 0.8g (2.0mmol) yellow-white.
Yield 85%.
The purity of gained compound is 99.5% (HPLC).
Embodiment 6 prepares paroxetine acetate from POT.mes
1.0g (2.4mmol) POT.mes is dissolved in the hot Virahol of 5ml.In this solution, add 0.2g (3.2mmol) acetate.Mixture placement under 4 ℃ is spent the night, after this be settled out solid.Cross filter solid and wash vacuum-drying 3 times with the 10ml ether.Obtain the crystallization of 0.5g (1.3mmol) yellow-white.
Yield 54%.
The purity of gained compound is 99.5% (HPLC).
Embodiment 7 prepares the paroxetine free alkali from POT.mes
10.0g (24.0mmol) POT.mes is dissolved in 150ml water and the 200ml ethyl acetate.To wherein adding 12.4g (31mmol) 10 (weight) % aqueous sodium hydroxide solution, and this suspension stirred 15 minutes.Separate 50ml ethyl acetate extraction 1 time of each layer and water layer.The organic layer that merges is with 100ml water washing 1 time and use dried over sodium sulfate.Filter sodium sulfate and use 50ml ethyl acetate washing 1 time.Evaporate ethyl acetate, obtain 7.5g (22.8mmol) oily product.
Yield 95%
The purity of this compound is 99.5% (HPLC).
Analyze a plurality of compounds of gained, it the results are shown among the following table 1-5:
Table 1 paroxetine and some organic sulfonic acid R-SO 3The salifiable feature of H
R=CH 3M.p.:142 '-144 ℃ of-(POT.mes). DSC curve (closed disk .10 ℃/minute): (kBr is with cm to start from 145.8 ℃ of .79.0J/g. IR spectrum -1Meter) 531,546,777,838,931.962.1038,1100,1169. 1208,1469,1500,1515,1615,2577,2869,2900,3023. 1H-NMR (ppm): 1.99 (br d, H 5eq,1H);2.27(ddd,H 5ax,1H);2.48-2.65(m,H 3, 1H);2.82-2.92(m,H 4,CH 3,4H);2.95-3.20(m,H 2ax,H 6ax,2H);3.47(dd, H 7,1H);3.58-3.74(m,H 2eq,H 6eq,H 7,3H);5.88(s,H 7″,2H);6.10(dd,H 6″, 1H);6.33(d,H 2″,1H);6.61(d,H 5″,1H);7.09(dd,H 3′,H 5′,2H);7.22(dd,H 2′, H 6′,2H);8.85(br?d,NH cq,1H);9.11(br?d,NH ax,1H). 13C-NMR(ppm);30.0(s,C 5);39.3(s,C 3);39.5(s,C 4);41.7(s,sC);44.6(s, C 6);46.8(s,C 2);67.4(s,C 7);97.8(s,C 2″);101.2(s,C 7″);105.4(s,C 6″);107.8 (s,C 5″);115.8(d,C 3′,C 5′);128.4(s,C 6′,C 2′);137.1(s,C 4″);142.0(s,C 1′); 148.2(s,C 3″);153.7(s,C 1″);161.9(d,C 4′).
R=C 6H 5Mp.:55 °-60 ℃ of-(paroxetine benzene sulfonates). (kBr is with cm for IR spectrum -1Meter): 530,564,614,689,728,764,828,929,993,1007,1029,1121,1179,1229,1443,1471,1486,1514,1600,1628,2557,2842,3029. 1H-NMR (ppm): 1.90 (br d, H 5eq,1H);2.10-2.28(m,H 5ax,1H);2.38-2.52(m, H 3,1H);2.82(ddd,H 4,1H);3.02-3.18(m,H 2ax,H 6ax,2H);3.37(dd,H 7,1H); 3.48(d,H 7,1H);3.60-3.82(m,H 2eq,H 6cq,2H);5.87(s,H 7″,2H);6.06(dd, H 6″,1H);6.29(d,H 2″,1H);6.60(d,H 5″,1H);6.90(dd,H 3′,H 5′,2H);7.04(dd, H 2′,H 6′,2H);7.40(d,ArH,3H);7.94(d,SArH,2H);8.81(br?d,NH cq,1H); 9.04(br?d,NH ax?1H). 13C-NMR(ppm):29.9(s,C 5);39.2(s,C 3);41.5(s,C 4);44.8(s,C 6);47.0(s, C 2);67.3(s,C 7);97.9(s,C 2″);101.2(s,C 7″);105.5(s,C 6″)107.8(s,C 5″); 115.7(d,C 3′,C 5′);125.9(s,C b);128.6(s,C d);128.8(s,C 6′,C 2′);130.6(s, C );137.1(s,C 4″);141.9(s,C 1′);144.1(s,C a);148.2(s,C 3″);153.7(s,C 1″); 161.8(s,C 4′).
R=p-CH 3C 6H 4(paroxetine tosilate) m.p.:148 °-150 ℃. DSC curve (closed disk, 10 ℃/minute): start from 151.6 ℃, 71.6 (kBr is with cm for J/g. IR spectrum -1Meter): 529,557,671,771,800,814,921,936,1000,1029,1100,1157,1186,1229,1471,1486,1507,1600,2557,2829,3029 1H-NMR (ppm): 1.89 (br d, H 5eq,1H);2.10-2.50(m,H 5ax,H 3,CH 3,5H);2.82 (ddd,H 4,1H):2.97-3.18(m,H 2ax,H 6ax,2H);3.36(dd,H 7,1H);3.48(dd,H 7, 1H);3.52-3.77(m,H 2eq,H 6eq,2H);5.87(s,H 7″,2H);6.06(dd,H 6″,1H);6.28
Table 1 (continuing) paroxetine and some organic sulfonic acid R-SO 3The salifiable feature of H
(d,H 2″,1H);6.59(d,H 5″,1H);6.90(dd,H 3′,H 5′,2H);7.05(dd,H 2′,H 6′,2H); 7.24(d,CH 3ArH,2H);7.83(d,SArH,2H);8.91(br?d,MH cq,1H);9.17(br?d, NH ax,1H). 13C-NMR(ppm):21.3(s,C e);29.9(s,C 5);39.2(s,C 3);41.5(s,C 4);44.7(s, C 6);46.9(s,C 2);67.3(s,C 7);97.8(s,C 2″);101.1(s,C 7″);105.5(s,C 6″);107.8 (s,C 5″);115.6(d,C 3′,C 5′);125.8(s,C b);129.0(s,C 6′,C 2′);129.1(s,C c); 137.2(s,C 4″);140.8(s,C d);141.5(s,C a);141.9(s,C 1′);148.2(s,C 3″);153.8 (s,C 1″);161.8(d,C 4′).
R=p-ClC 6H 4(paroxetine closilate) m.p.:75 °-80 ℃. (kBr is with cm for IR spectrum -1Meter) 486,557,643,736,821,1000,1029,1086,1114,1186,1229,1471,1486,1514,1600,1657,2857,3029. 1H-NMR (ppm): 1.91 (br d, H 5eq,1H);2.15(ddd,H 5ax,1H);2.37-2.52(m,H 3, 1H);2.81(ddd,H 4,1H);2.93-3.21(m,H 2ax,H 6ax,2H):3.37(dd,H 7,1H);3.49 (d,H 7,1H);3.61-3.81(m,H 2eq,H 6eq,2H);5.88(s,H 7″,2H);6.05(dd,H 6″, 1H);6.27(d,H 2″,1H);6.59(d,H 5″,1H);6.91(dd,H 3′,H 5′,2H);7.03(dd,H 2′, H 6′,2H);7.39(d,ClArH,2H);7.86(d,SArH,2H);8.78(br?d,NH eq,1H); 9.02(br?d,NH ax,1H). 13C-NMR(ppm);30.0(s,C 5);39.3(s,C 3);41.5(s,C 4);44.9(s,C 6);47.1(s, C 2);67.3(s,C 7);97.9(s,C 2″);101.2(s,C 7″);105.5(s,C 6″);107.9(s,C 5″); 115.8(d,C 3′,C 5′);127.6(s,C b);128.8(s,C 6′,C 2′);132.0(s,C d);137.0(s,C c); 137.2(s,C 4″);141.8(s,C 1′);142.0(s,C a);148.2(s,C 3″);153.6(s,C 1″);161.8 (d,C 4′).
Compound of the present invention is crystallization, has definite fusing point, DSC curve and IR spectrum.Under its different formation condition and under the specified conditions, can not get rid of these compounds and can also have other crystallization or polymorphic variant different with those crystallizations described here.The generally very stable and no hygroscopicity of compound of the present invention.
Should be understood that not conform to basically the bonded organic solvent is arranged with organic sulfonic acid synthetic acid salt of the present invention.In anhydrous compound, the content of preferred combination organic solvent is less than 2.0% (w/w).But they can also contain crystal water and not combination water, the just water except that crystal water.
In following table 2 and 3, provide wettability test and stability test (comparing) result's example with known paroxetine salt.
The water absorbability of some paroxetine salt of table 2 (40 ℃, 75% relative humidity)
0.35+0.04 pair-toluene fulfonate of moisture (%) t=0 t=4 week mesylate, 0.70<0.02 hydrochloride-+2.5
The solubleness (mg/ml) of table 3 paroxetine salt in water
20 ℃ of 50 ℃ of mesylates>1,000 1300 pair-toluene fulfonate>1000>1000 hydrochloride semihydrates, 4.9 12.6 anhydrous salt hydrochlorates 8.2 24.2
The paroxetine salt-stable that table 4 is measured by HPLC (total degradation amount, %)
The 20 ℃ of 80 ℃ of mesylates of degrading do not observe<and 0.2%, 3 months right-tosylates do not observe<and 0.2%, maleate 0.2% in 3 months, 12 months>50%, 5 day
The solubleness (mg/ml) of table 5 paroxetine salt in non-aqueous solvent
Mesylate is right-20 ℃<0.05<0.05 69 ℃ 0.05<0.05 of 20 ℃ 2 22 77 ℃ 25>500 n-hexane of 20 ℃ 5 16 56 ℃ 37 125 ethyl acetate of 20 ℃ 7 14 82 ℃ 330>500 acetone of 20 ℃ 36 50 78 ℃ 250>500 2-propyl alcohol of toluene fulfonate ethanol
The example of the paroxetine salt for preparing in embodiment 5-7 and the analytical data of free alkali is listed in the table 6.
The feature of table 6 paroxetine salt/free alkali
Paroxetine maleate: m.p.:128-130 ℃. 1H-NMR (ppm): 1.65-2.00 (m, H 5eq,H 5ax,2H);2.00-2.50(m,H 3,1H);2.55- 3.15(m,H 2ax,H 6ax,H 4,3H);3.15-3.75(m,H 2eq,H 6eq,H 7,3H);5.67(s,H 7″, 2H);5.97(s,H a,1H);6.12(dd,H 6″,1H);6.42(d,H 2″,1H);6.67(d,H 5″,1H); 6.95-7.35(m,H 2′,H 3′,H 5′,H 6′,4H).
Paroxetine acetate: m.p.:123-125 ℃. 1H-NMR (ppm): 1.70-2.00 (m, H 5eq,H 5ax,2H);1.97(s,H 2,3H);2.05-2.50(m, H 3,1H);2.50-3.00(m,H 4,H 2ax,H 6ax,3H);3.05-3.75(m,H 2eq,H 6eq,H 7,3H); 6.05(s,H 7″,2H);6.28(dd,H 6″,1H);6.58(d,H 2″,1H);6.65(d,H 5″,1H);7.10- 7.50(m,H 2′,H 3′,H 5′,H 6′,4H).
Paroxetine 1H-NMR (ppm): 1.60-2.00 (m.H 5ax,H 5eq,2H);2.00-2.35(m,H 3,1H);2.40- 2.95(m,H 4,H 2ax,H 6ax,3H);3.15-3.70(m,H 2eq,H 6eq,H 7,2H);5.67(s,H 7″, 2H);6.11(dd,H 6″,1H);6.43(d,H 2″,1H);6.62(d,H 5″,1H);6.80-7.35(m,H 2′, H 3′,H 5′,H 6′,4H).
Obviously, the present invention is not limited to above-mentioned explanation, and as following claims regulation.Reference
Psychopharmacology, 57,151-153 (1978); Ibid, and 68,229-233 (1980),
Europe pharmacology magazine, 47,351-358 (1978),
Among the USP 4007196 " preparation of paroxetine maleate " of report.

Claims (17)

1. the compound and pharmacologically acceptable salt or the solvate that have formula I:
Figure C9718223700021
Wherein-R represents 3 ' 4 '-methylene radical-dioxy base phenyl;-R 1Represent hydrogen or C 1-C 4Alkyl;-X represents hydrogen or halogen;-R 2Representative-C1-C10 alkyl ,-by the optional phenyl that replaces of or several following groups:
-C1-C10 alkyl,
-halogen.
2. the described compound of claim 1, wherein radicals R is 3,4-methylene radical-dioxy base phenyl, and R 1Represent hydrogen.
3. claim 1 or 2 described compounds, wherein radicals X is the fluorine that is connected on 4 of the phenyl ring.
4. claim 1 or 2 described compound, wherein R 2It is the C1-C4 alkyl.
5. claim 1 or 2 described compound, wherein R 2It is the C1-C2 alkyl.
6. claim 1 or 2 described compounds, wherein X is the fluorine in contraposition, R is 3,4-methylenedioxyphenyl base, R 1Be hydrogen and R 2It is methyl.
7. claim 1 or 2 described compounds are selected from:
-POT.mes,
-paroxetine benzene sulfonate,
-paroxetine is right-tosylate,
-paroxetine is right-closilate.
8. the preparation method of each described compound of claim 1-7, the step of this method comprises: will be suc as formula the compound shown in the II, its salt and/or alkali and general formula R 2-SO 3Sulfonic acid shown in the H mixes in solvent, forms a solution, isolates formed solid subsequently, in formula II:
Figure C9718223700031
Wherein :-R represents 3 ' 4 '-methylene radical-dioxy base phenyl;-R 1Represent hydrogen or C 1-C 4Alkyl;-X represents hydrogen or halogen; At general formula R 2-SO 3Among the H-R 2Representative
-C 1-C 10Alkyl,
-by the optional phenyl that replaces of one or more following groups:
-C 1-C 10Alkyl,
-halogen.
9. according to the method for claim 8, further comprise the step of the solvate forms that obtains each described compound of claim 1-7, this step comprises: with each described compound of claim 1-7 with mainly be selected from following reagent mix together: water, methyl alcohol, ethanol.
10. according to the method for claim 8, further comprise the step of the pharmaceutical acceptable salt that obtains each described compound of claim 1-7, this step comprises: each described compound of claim 1-7 is mixed with organic and/or mineral acid.
11. according to the method for claim 10, wherein said acid mainly is selected from:
Hydrochloric acid methyl ethyl oxalate sulfonic acid
Hydrogen bromide succsinic acid Phenylsulfonic acid
Hydroiodic acid HI tartrate tosic acid
Acetic acid citric acid p-chlorobenzenesulfonic acid
Propionic acid is pounced on acid/pamoic acid
Toxilic acid sulfuric acid
Fumaric acid.
12. according to the method for claim 8, further comprise the step of the free alkali that obtains each described compound of claim 1-7, this step comprises: each described compound of claim 1-7 and organic and/or mineral alkali are mixed.
13. the described method of claim 12, wherein said alkali mainly is selected from following material: sodium hydroxide, potassium hydroxide, calcium hydroxide, ammonium hydroxide, yellow soda ash, methylamine, dimethylamine, triethylamine, pyridine.
14. contain the medicine of each described compound of claim 1-7, its pharmacologically acceptable salt or solvate and pharmaceutically acceptable carrier/thinner.
15. the medicine of claim 14, it is tablet, coated tablet or capsular form.
16. the application of each described compound of claim 1-7 in the preparation medicine.
The dysthymia disorders that 17. the application of claim 16, wherein said medicine are used for the treatment of dysthymia disorders, obsessional idea and behavior disorder disease, Phobias, Bulimia nerovsa, apocleisis, pain, obesity, senile dementia, migraine, anorexia, social phobia, the preceding anxiety of passing through causes.
CN97182237A 1997-06-10 1997-06-10 4-phenylpiperidine compound Expired - Fee Related CN1092654C (en)

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US4007196A (en) * 1973-01-30 1977-02-08 A/S Ferrosan 4-Phenylpiperidine compounds

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4007196A (en) * 1973-01-30 1977-02-08 A/S Ferrosan 4-Phenylpiperidine compounds

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