Isolation of Uteroevacuant Substances From Plant Extracts

In co-pending application Ser. No. 672,918, now U.S. Pat. No. 4,086,358 a method is described for isolating and purifying the active principles in the zoapatle plant. These materials have been shown to possess uteroevacuant properties. In the process described in the above-noted application, a crude extract is first obtained by a series of extraction and purification steps and the crude extract is further purified by chromatography over silicic acid. As a result of the chromatography, a semi-purified mixture containing at least three major components is obtained. This mixture is then chromatographed through a column of a polymeric gel. A number of fractions are collected and the composition of each fraction is monitored by either gas chromatography or thin layer chromatography. As a result of the second chromatogram, two chemically distinct compounds are obtained as evidenced by gas chromatography and spectral analyses. These copounds have the following formulae. ##STR1##

The present invention relates to a chemical method of isolating, separating and purifying crude extracts or semi-purified mixtures obtained from the zoapatle plant to obtain the biologically-active compounds.

The zoapatle plant is a bush about 2 m. high that grows wild in Mexico. Botanically it is known as Montanoa tomentosa according to Cervantes, Fam. Compositae, Tribe Heliantheae; another variety of the species is Montanoa floribunda. The plant is described in great detail in Las Plantas Medicinales de Mexico, third edition, Ediciones Botas (1944).

The plant has been used for centuries in the form of a "tea" or other crude aqueous preparations primarily as a labor inducer or menses inducer for humans. Its use as a uteroevacuant agent has been documented in the literature, but definitive chemical and pharmacological studies have not been described. By uteroevacuant is meant an agent which causes the uterus of warm blooded animals to contract or expel its contents. Such agents are generally employed to induce menses, expel a hydatiform mole, expel or resorb a fetus, induce abortion or delayed labor and in situations in which the contents of the uterus, such as the fetus or placenta, should be evacuated.

The process of the present invention is illustrated by the following reaction sequence wherein R is an acyl group derived from an aliphatic acid. ##STR2##

As the starting material in the process of the present invention, either the crude extract or the semi-purified material containing at least three major components obtained as described in Ser. No. 672,918 can be employed. The semi-purified residue is first converted to the acyl derivatives by reaction with an excess of an acyl halide or an acid anhydride. The acylation step is preferably carried out in the presence of a base. Acyl halides or acid anhydrides having 1-10 carbon atoms in the acyl group may be employed. The preferred acylating agents are the acetyl, propionyl, butyryl and valeryl halides and the corresponding anhyrides. Bases which may be employed in the acylation step include trialkylamines such as triethylamine, trimethylamine and tripropylamine, and tertiary amines such as pyridine, N,N-dimethylaniline and N,N-diethylaniline. The reaction is preferably carried out in an inert atmosphere such as nitrogen or argon, for example, and at a temperature between about 0.degree.-30.degree. C. The reaction may be carried out in an organic solvent such as, for example, benzene, ether, tetrahydrofuran, toluene and the like. The acylated materials are obtained from the reaction mixture by techniques known to those skilled in the art. For example, the organic base can be removed by extraction with a dilute aqueous acid solution or an aqueous saturated copper sulfate solution. The crude mixture of acyl derivatives is then obtained by removal of the solvent.

Treatment of the mixture of acyl derivatives with an excess of reducing agent such as sodium borohydride or lithium tritertiarybutoxy aluminum hydride, for example, converts the compounds to the hydroxy derivatives (III-a and III-b). The reduction step is preferably carried out in an inert atmosphere, such as nitrogen or argon, and in an organic solvent such as ethanol, methanol or tetrahydrofuran. The particular solvent employed will depend upon the particular reducing agent employed in the reaction. It is preferred to carry out the reaction at room temperature, however, temperatures as low as 0.degree. C may be employed in the reduction step. The reaction mixture is generally quenched with dilute aqueous acids such as, for example, dilute hydrochloric acid or a saturated ammonium chloride solution. After removal of the solvent, the crude mixture of hydroxy derivatives is used as such in the next step.

Treatment of the mixture of hydroxy derivatives with an oxidizing agent such as manganese dioxide selectively oxidizes III-b to II-b. It is preferred to carry out the reaction at room temperature with an excess of the oxidizing agent, although elevated temperatures may be employed. The reaction may be carried out in an organic solvent such as methylene chloride, chloroform, hexane or benzene. The compounds are then separated by physical means. For example, the inorganic materials can be removed by filtration and the residue left after removal of the solvent can be chromatographed over an adsorbent material such as silica gel to afford III-a and II-b.

The hydroxy derivative (III-a) is converted to the corresponding ketone (II-a) by treatment with a suitable oxidizing agent such as a mixture of chromium trioxide-sulfuric acid and chromium trioxide-pyridine. The reaction is preferably carried out in an inert atmosphere such as nitrogen or argon, for example, at a temperature of about 0.degree. C, although lower temperatures may also be employed. The reaction is generally carried out in an organic solvent such as acetone, 2-butanone, methylene chloride or chloroform, depending upon the particular oxidizing agent employed. The acetyl derivative (II-a) is converted to the underivatized uteroevacuant material (I-a) by hydrolysis with a suitable base such as, for example, sodium hydroxide, potassium hydroxide or tetra n-butyl ammonium hydroxide. The reaction is preferably carried out in an inert atmosphere such as nitrogen or argon at room temperature; however, temperatures as high as the reflux temperature of the solvent may also be employed. Methanol, ethanol, isopropanol, benzene, ether or tetrahydrofuran may be employed as the solvent. Aqueous media may also be employed. The crude product (I-a) can be further purified by column chromatography over an adsorbent material such as silica gel, alumina or florisil.

The acetyl derivative first obtained above (II-b) is converted to the underivatized uteroevacuant material (I-b) by hydrolysis with a suitable base as described above. The crude product (I-b) can be further purified by column chromatography over an adsorbent material such as silica gel, alumina or florisil. The presence of uteroevacuant materials in the products obtained from the reactions is determined through procedures employed for the detection of uterine contractions and interruption of pregnancy. The compounds are identified by thin layer chromatography and spectral analysis.

The purified compounds are effective in inducing uterine contractions when administered in doses ranging from about 1.0 mg. to about 85 mg./kg. The purified compounds are effective in interrupting pregnancy at dosage levels between about 15 to about 100 mg./kg. The preferred dosage range is from about 20-85 mg./kg. As central nervous system depressants, the compounds are active in doses as low as 3.7 mg./kg. The actual dosage employed will depend upon the species of animal to which the compound is administered. The compounds can be administered in formulations prepared according to acceptable pharmaceutical practices. Suitable formulations include solutions, suspensions and solid dosage forms in pharmaceutically acceptable carriers. They can be administered perorally or intravenously or in any conventional manner in accordance with acceptable pharmaceutical practices.

The semi-purified starting material (1.172 g.) is dissolved in a solution of benzene (30 ml.) and pyridine (10 ml.) and the solution is treated while stirring at 0.degree. C with acetyl chloride (5 ml.) under nitrogen. The reaction mixture is allowed to warm to room temperature and is stirred for 4 hrs. The resulting mixture is treated with ice water (10 ml.) and ether (200 ml.). The organic layer is washed and saturated cupric sulfate solution (3 .times. 100 ml.) and dried (MgSO.sub.4). After removal of the solvent in vacuo, the crude mixture of II-a and II-b (1.212 g.) is used as such in the next step.

The mixture (1.212 g.) obtained in A above is dissolved in methanol (100 ml.) and treated with sodium borohydride (400 mg.) at room temperature under nitrogen. The resulting mixture is stirred for 5 mins. and then treated with a saturated ammonium chloride solution (100 ml.). The aqueous mixture is extracted with methylene chloride (300 ml.). The organic layer is dried (MgSO.sub.4) and then evaporated in vacuo to give a yellow oil (1.1 g.) The crude mixture of III-a and III-b is used as such in the next step.

The crude mixture (III=a and III-b) obtained in B above (1.1 g.) is dissolved in methylene chloride (100 ml.) and the resulting solution is treated at room temperature with manganese dioxide (4 g.). The resulting mixture is stirred for 16 hrs. and then filtered through a pad of celite. The organic layer is dried (MgSO.sub.4) and evaporated in vacuo to yield a yellow oil. The oil is chromatographed on a SilicAR (a neutral silica gel product sold by Mallinckrodt, Inc., St. Louis, Missouri) column (20 g.). The keto derivative II-b (243 mg.) is eluted with 25:75 ether-petroleum ether; the hydroxy derivative III-a (754 mg.) is eluted with 75:25 ether-petroleum ether. The spectral characteristics of II-b and III-a are as follows:

II-b - I.R. (Neat) .mu. : 5.75, 5.95, 6.2 and 8.1; N.M.R. (CDCl.sub.3) .delta.: 6.03 (bs, 1H, ##STR3## 5.35 (m, 1H, >C.dbd.CH--CH.sub.2 --O); 4.62 (d, J=6Hz, >C.dbd.CH--CH.sub.2 OAc); 4.08 (bs, 2H ##STR4## 2.03 (s, 6H, ##STR5##

III-a - I.R. (Neat) .mu. : 2.86 and 5.75;

N.m.r. (cdcl.sub.3) .delta.: 5.3 (m, 2H, >C.dbd.CH--CH.sub.2 OAc and ##STR6## 4.7 (d, J=6Hz, 2H, >C.dbd.CH--CH.sub.2 --OAc); 4.1 (bs, 2H ##STR7## 3.45 (m, 1H, Ac--O--CH<); 2.03 (s, 6H, ##STR8##

The hydroxy derivative (III-a, 333 mg.) obtained as in C above is dissolved in acetone (5 ml.) and treated slowly with Jones reagent (2 mmole) at 0.degree. C under nitrogen. The resulting mixture is stirred for 7 mins, and then treated with ether (30 ml.) and water (20 ml.). The layers are separated and the aqueous layer is extracted with ether (20 ml.). The combined organic layer is washed with water (30 ml.), dried (MgSO.sub.4) and evaporated in vacuo to give an oil. The crude product (II-a) is used as such as in the next step.

The crude product (II-a) obtained in D above (161 mg.) is dissolved in tetrahydrofuran (5 ml.) and water (5 ml.). To this mixture, tetra n-butyl ammonium hydroxide (20% solution in methanol, 1 ml.) is added under nitrogen at room temperature and the result mixture is stirred for 40 hours. The mixture is treated with 50 ml. of ether and the organic layer is washed with 10% hydrochloric acid (2 .times. 15 ml.), dried (MgSO.sub.4) and evaporated in vacuo to give an oil. This crude product is purified by chromatography on a SilicAR column (5 g.). The compound I-a (81.8 mg.) is eluted with ether. Its ir, nmr spectra, R.sub.f on thin layer and retention time on gas chromatography are identical to those of compound I reported in co-pending application Ser. No. 672,918. The compound has the following spectral characteristics:

I.R. (Neat) .mu. : 2.91 and 5.88; N.M.R. .sub.TMS.sup.CDCl.sbsp.3 .delta. : 5.41 (m, 2H, >C.dbd.CH--CH.sub.2 OH and ##STR9## 4.20 (d, 2H, >C.dbd.CH.sub.13 CH.sub.2 OH); 4.15 (s, 2H, ##STR10## 3.58 [broad t, 1H, >CH(OH]; 3.18 (d, 2H, ##STR11## 1.71 [d, 6H, >C.dbd.C--(CH.sub.3).sub.2 ]; 1.15 (s, 3H ##STR12##

Mass spec [m/e]: 320 [M-18] , 251, 233, 221, 171, 143, 141, 137, 125, 113, 97, 95, 81, 69

Chemical Ionization: M.sup.+ + H = 339; M.W. = 338.

The keto derivative (II-b) obtained as in C above (243 mg.) is dissolved in tetrahydrofuran (5 ml.) and water (5 ml.). To this mixture tetra n-butyl ammonium hydroxide (20% solution in methaol, 1.5 ml.) is added under nitrogen at room temperature and the resulting mixture is stirred for 16 hrs. The mixture is treated with 50 ml. of ether and 20 ml. of water. The organic layer is separated, dried (MgSO.sub.4) and evaporated in vacuo to give an oil. This crude product is further purified by chromatography on a SilicAR column (10 g.). The product I-b (152 mg.) is eluted with ether. Its ir, nmr spectra, R.sub.f on thin layer and retention time on gas chromatography are identical to those of compound II, reported in co-pending application Ser. No. 672,918. The compound has the following spectral characteristics:

I.R. (Neat) .mu. : 2.90, 5.96 and 6.21; N.M.R. .sub.TMS.sup.CDCl.sbsp.3 .delta.: 6.11 (broad s, 1H, ##STR13## 5.48 (m, 1H, >C.dbd.CH--CH.sub.2 OH); 4.19 (d, 2H, >C.dbd.CH--CH.sub.2 OH); 4.13 (s, 2H ##STR14## 3.56 [broad t, 1H, ##STR15## 2.10 (d, 3H, ##STR16## 1.13 (s, 3H, ##STR17## 1.07 [d, 6H, ##STR18##

Mass Spec [m/e]: 334 [M-18] , 225, 240, 111, 95, 81, 69.

U.V. - A max (EtOH): .about. 239 nm [.epsilon.=8500] .

Chemical Ionization: M.sup.+ + H = 353; M.W. = 352.

Ten kg. of dried or fresh leaves from the zoapatle plant (Mantanoa tomentosa) and 30 gallons of water are added to a 100 gallon steam-jacketed stainless steel tank. The mixture is heated at 90.degree.-100.degree. C for 2.5 hours with periodic stirring. The hot mixture is filtered through gauze to afford a clear dark tea, about 25 gallons in volume. The solid residue in the tank is washed with 4 gallons of hot water, filtered, and the filtrate combined with the tea obtained above. The combined aqueous extracts are extracted with 30 gallons of ethyl acetate. The mixture is stirred vigorously and allowed to settle. The top frothy layer is siphoned off to break the emulsion, and as much ethyl acetate separated as possible. Another 20 gallons of ethyl acetate are added to the mixture and the above process repeated. The combined ethyl acetate extracts are evaporated at 50.degree. C under vacuum. The residue is extracted with three portions of hot (75.degree.-80.degree.) benzene (10 liters total). The benzene extracts are evaporated at 50.degree. C under vacuum and the residue is washed three times with a total of 8 liters of refluxing hexane. The hexane-washed residue is dissolved in 2 liters of acetone, 10 g. of Nuchar is added, and the mixture is stirred for 1 hour at room temperature. The charcoal is removed by filtration, and the filtrate evaporated by distillation at 30.degree. C under vacuum to afford 69 g. of crude extract.

The crude residue obtained in A above (50 g.) is dissolved in ether (5 l.) and the resulting solution is filtered and washed with saturated sodium bicarbonate solution (500 ml.). The ether is dried over anhydrous sodium sulfate, filtered and concentrated to dryness to afford a light yellow oil (44.6 g.). This oil is then dissolved in chloroform (400 ml.) and the solution added to a column (4 in. .times. 4 ft.) of 2.5 kg. of neutral silicic acid packed in chloroform. The column is eluted with chloroform, chloroform-isopropanol mixtures, and 110 fractions are collected. The fractions are evaporated to dryness in vacuo at a temperature below 40.degree. C. The column is eluted as follows:

The composition of the fractions is monitored by thin layer chromatography [silica gel, isopropanol-chloroform (1:12.5)] and by gas chromatography -- 3% OV17 [methyl silicone - phenyl silicone (1:1)] column using a programmed run (150.degree.-250.degree.). Fractions Nos. 78-84 are combined and the solvent removed in vacuo to afford an oily residue (5.1 g.) which contains at least three major components as indicated by gas chromatography.

A portion of the residue (3.2 g.) is then dissolved in benzene (50 ml.) and the solution added to a column (4 in. .times. 35 in.) packed with 2 kg. of OR-PVA Merck-O-Gel 2000 (A vinyl acetate copolymer which swells in organic solvents, produced by E. M. Merck, Inc. and sold under the trademark EM Gel.RTM. Type OR-PVA.) prepared in benzene. The column is eluted with benzene and a total of 47 fractions is collected. Thin layer chromatography and gas chromatography are used to monitor the composition of the fractions.

Fractions 23-33 contain 1.73 g. (54%) of the applied material.

(1) Fractions 24-25 are evaporated to give compound I-b as an oil (0.251 g.).

(2) Fraction 31 is evaporated to give compound I-a as an oil (0.326 g.).

The following general procedure is a standard procedure employed to detect uterine contractions in female animals.

Mature female New Zealand rabbits are anesthetized with sodium pentobarbital and ovariectomized. Following a recovery period of one week, the rabbits are treated with 8 .mu.g./day s.c. of 17.beta.-estradiol for 6 consecutive days, followed by treatment with 1.0 .mu.g./day s.c. of progesterone for 7 consecutive days. The uterus and oviducts of the rabbits are perfused 72 hours after the last dose of progesterone according to the method of Heilman, et al., (Fertil. Steril. 23:221-229) with slight modifications. The oviduct and uterus are perfused at a rate of 53 .mu.l./min. The uterus is perfused with a tube extending 1.0 cm. into the lumen of the uterus from the oviducal end. The uterus is ligated at the utero-tubal junction. Another cannula is inserted 1.0 cm. into the uterus through a small incision in the vagina in order to collect perfusate. The material to be tested is administered i.v. through the jugular vein in a vehicle that contains polyethylene glycol 200, polyethylene glycol 400, ethanol and a phosphate buffer. The cannula is attached to a P23-Dc Stathan transducer which in turn is coupled to a Grass Model 5 polygraph and the uterine contractility measured.

Intravenous administration of the compound obtained from Fraction 31 (I-a) is effective in inducing uterine contractions and relaxing the oviduct in 72-hour progesterone withdrawn rabbits in a dose range of 1.0-4.0 mg./kg. The compound obtained from Fractions 24-45 (I-b) is effective when administered in a dose range of from 25-40 mg./kg.

The following general procedure is a standard procedure employed to detect interruption of pregnancy after implantation has occurred.

Mature, Hartley strain, female guinea pigs are continuously cohabited (monogamously) with males until a vaginal plug (copulation plug) is found in the cage. This time is considered to be day 1 of gestation. Groups of 5-6 females are given test materials intraperitoneally in the vehicle described in Procedure I on day 22 of gestation. The pigs are sacrificed between the 25th and 45th day of gestation and examined for evidence of resorption or abortion.

Intraperitoneal administration of the material obtained from Fraction 31 (I-a) is effective in interrupting pregnancy when administered in a dose range from 25-85 mg./kg.