Patent Grant
8293947
1. Field of the Invention
This invention relates to the preparation of two triphenylbutene derivatives, valuable in therapy as selective estrogen receptor modulators.
2. Description of Related Art
The publications and other materials used herein to illuminate the background of the invention, and in particular, cases to provide additional details respecting the practice, are incorporated by reference.
“SERMs” (selective estrogen receptor modulators) have both estrogen-like and antiestrogenic properties (Kauffman & Bryant, Drug News Perspect. 8:531-539, 1995). The effects may be tissue-specific as in the case of tamoxifen and toremifene which have estrogen-like effects in the bone, partial estrogen-like effect in the uterus and liver, and pure antiestrogenic effect in breast tissue. Based on the published information, many SERMs are more likely to cause menopausal symptoms than to prevent them. They have, however, other important benefits in elderly women: they decrease total and LDL cholesterol, thus minimizing the risk of cardiovascular diseases, and they may prevent osteoporosis and inhibit breast cancer growth in postmenopausal women.
Ospemifene, (Z)-2-[4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenoxy]ethanol, which is one of the main metabolites of toremifene, is known as an estrogen agonist and antagonist (Kangas, Cancer Chemother. Pharmacol. (1990) 27:8-12; WO 96/07402 and WO 97/32574). Ospemifene has relatively weak estrogenic and antiestrogenic effects in the classical hormonal tests (Kangas, 1990). It has anti-osteoporosis actions and it decreases total and LDL cholesterol levels in both experimental models and in human volunteers. It also has antitumor activity in an early stage of breast cancer development in an animal breast cancer model. Ospemifene is also the first SERM which has been shown to have beneficial effects in climacteric syndromes in healthy women. The use of ospemifene for the treatment of certain climacteric disorders and atrophy-related diseases or disorders in postmenopausal women is disclosed in WO 02/07718 and WO 03/103649.
WO 01/36360 describes a group of SERMs, which are tissue-specific estrogens and which can be used in women in the treatment of climacteric symptoms, osteoporosis, Alzheimer's disease and/or cardiovascular diseases without the carcinogenic risk. Certain compounds can be given to men to protect them against osteoporosis, cardiovascular diseases and Alzheimer's disease without estrogenic adverse events (gynecomastia, decreased libido etc.). Of the compounds described in said patent publication, the compound (Z)-2-{2-[4-(4-chloro-1,2-diphenylbut-1-enyl)phenoxy]ethoxy}ethanol (also known under the generic name fispemifene) has shown a very interesting hormonal profile suggesting that it will be especially valuable for treating disorders in men. WO 2004/108645 and WO 2006/024689 suggest the use of fispemifene for treatment or prevention of age-related symptoms in men, such as lower urinary tract symptoms and diseases or disorders related to androgen deficiency in men.
Known methods for the syntheses of compounds like ospemifene and fispemifene include rather many steps. WO 02/090305 describes a method for the preparation of fispemifene, where in a first step a triphenylbutane compound with a dihydroxy substituted butane chain is obtained. This compound is in a second step converted to a triphenylbutene where the chain is 4-chlorosubstituted. Then the desired Z-isomer is crystallized. Finally, the protecting group is removed to release the ethanol-ethoxy chain of the molecule.
In the known methods, the separation of the desired Z isomer is tedious. The protection group used to protect the ethanol-ethoxy chain during the reaction steps, benzyl, is rather difficult to remove.
Both ospemifene and fispemifene are likely to be commercialized in the near future. Thus, there is a great need for powerful methods for the preparation of these compounds in large scale.
Another object is to provide methods having common features so that the syntheses of the compounds easily can be run by using the same kind of equipment and materials.
Thus, according to one aspect, this invention concerns a method for the preparation of a compound of formula (Ia) or (Ib):
wherein a compound of formula (II)
a) is alkylated with an alkylating reagent of the formula X—(CH2)2—O—(CH2)2—O—Pr,
where X is Cl, Br, I, mesyloxy or tosyloxy, and Pr is a protecting group, to give a compound of formula (III)
which is subjected to removal of the protecting group Pr to give the compound of formula (Ia), or
b) is alkylated with an alkylating reagent of the formula X—(CH2)2—O—Pr, where X is Cl, Br, I, mesyloxy or tosyloxy, and Pr is a protecting group, to give a compound of formula (IV)
which is subjected to removal of the protecting group Pr to give the compound of formula (Ib), or
c) is alkylated with an alkylating reagent of the formula X—CH2—COOR, wherein X is Cl, Br, I, mesyloxy or tosyloxy, and R is an alkyl, to give a compound of formula (V)
and the ester is reduced to give the compound of formula (Ib).
Fispemifene is the Z-isomer of the compound of formula (Ia)
and ospemifene is the Z-isomer of the compound of formula (Ib)
The common starting material in the syntheses of (Ia) or (Ib), namely compound (II), is previously known (Toivola, 1990; EP 0095875). According to a method disclosed in EP 095875, this compound was prepared by dealkylation of a corresponding ether to give (II). The method may be used to produce a mixture of isomers of compounds (Ia) and (Ib), but most preferably is used to prepare the pure E- and Z-isomers of those compounds.
Particularly in case Z-isomers of the compounds (Ia) or (Ib) are desired, a preferable method for the synthesis of compound (II) is a McMurry reaction of commercially available starting materials, 4-hydroxybenzophenone with 3-chloropropiophenone. The McMurry reaction is a well-known reductive coupling of ketones involving two steps: (1) a single electron transfer to the carbonyl groups from an alkali metal, followed by (2) deoxygenation of the 1,2-diol with low-valent titanium to yield the alkene. This reaction produces mainly the Z-isomer of compound (II).
The alkylation in steps a) and b) is carried out in an organic solvent, preferably carried out in tetrahydrofuran. It is also preferable to add a base to the solvent, most preferably sodium hydride.
The step of alkylation is performed at a temperature and a time to achieve substantial alkylation of compound II.
The protecting group Pr can be any suitable protecting group such as benzyl, substituted benzyl, allyl, tetrahydropyranyl or any other alcohol protecting group obvious to one skilled in the art; see for example Protecting Groups in Organic Synthesis, Third Edition, T. W. Greene and P. G. M. Wuts. Wiley Interscience, 1999 pp 23-200. In a preferable embodiment the protecting group is tetrahydropyranyl. This protecting group is very easily removable by methods known to those of ordinary skill in the art. For example, acid labile alcohol protecting groups such as a tetrahydropyranyl group (e.g., 2-tetrahydropyranyl) can be removed using acid such as HCl. A benzyl group can be removed using methods such as hydrogenation with Pd on carbon as a catalyst, or reacting with Zn powder and acetyl chloride.
X is preferably I or Br in the alkylating reagent in steps a) and b).
In the alkylating reagent in step c) X is preferably I, Br, or Cl, most preferably Br.
The alkyl substituent R in the alkylating reagent in step c) is preferably a C1-4-alkyl, most preferably ethyl.
The reduction of compound (V) obtained in step c) is carried out with a reducing agent, preferably lithium aluminum hydride. Other reducing agents are well known to those of ordinary skill in the art.
The steps of the methods described herein are carried out at temperatures and for times sufficient to achieve the desired compounds (Ia) and (Ib). The selection of the parameters based on the disclosure herein can readily be made by one of ordinary skill without undue experimentation.
To sum up, the preferred embodiments according to the present invention provides considerable advantages over known methods for producing compounds of formula (Ia) or (Ib):
The invention will be illuminated by the following non-restrictive Examples.
Zinc (15.0 g, 0.23 mol) and tetrahydrofuran (THF) (180 ml) was added to the reaction vessel and cooled to −10° C. Titan tetrachloride was added dropwise to the mixture (21.6 g, 0.114 mol) at about −10° C. After the addition was completed the mixture was refluxed for two hours. Then the mixture was cooled to 40° C. and 4-hydroxybenzophenone (7.68 g, 0.039 mol) and 3-chloropropiophenone (6.48 g, 0.039 mol) dissolved in THF (75 ml) were added to the mixture. Refluxing was continued for additional 3.5 hours. The cooled reaction mixture was poured in aqueous potassium carbonate solution (21 g K2CO3+210 ml water) and allowed to stand overnight at the ambient temperature. The mixture was filtered and the precipitate was washed with THF. The filtrate was evaporated to dryness. The residue was dissolved in ethyl acetate and washed with water. Ethyl acetate phase was evaporated to dryness and the residue was crystallized first from methanol-water (8:2) and then from methanol-water (9:1). Yield 5.4 g.
Z-isomer: 1H NMR (CDCl3): 2.92 (t, 2H, ═CH2CH2Cl), 3.42 (t, 2H, ═CH2CH2Cl), 6.48 (d, 2H, aromatic proton ortho to hydroxy), 6.75 (d, 2H, aromatic proton meta to hydroxy), 7.1-7.4 (m, 10H, aromatic protons)
4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenol (0.33 g, 0.001 mol) was dissolved in tetrahydrofuran (3 ml) under a nitrogen atmosphere. Sodium hydride (0.036 g, 0.0015 mol) was added to the solution and the mixture was stirred at room temperature for an hour. 2-[2-(2-iodo-ethoxy)-ethoxy)-tetrahydropyran (0.6 g, 0.002 mol) was added and the mixture was refluxed for 3 hours. After cooling and adding water the mixture was extracted three times with ethyl acetate. The organic phase was dried with sodium sulphate and evaporated to dryness. The residue was used in the next reaction step without further purification.
The residue of the previous reaction step (Example 2) was dissolved in ethanol (10 ml) and the solution was acidified with 2 N aqueous hydrogen chloride. The mixture was stirred over night at ambient temperature. Then the solvent was evaporated, water was added and the mixture was extracted three times with dichloromethane. The organic phase was washed with water, dried with sodium sulphate and evaporated to dryness. The residue was crystallized from heptane-ethyl acetate (8:2). Yield 0.216 g.
Z-isomer, 1H NMR (CDCl3): 2.92 (t, 2H, ═CH2CH2Cl), 3.42 (t, 2H, ═CH2CH2Cl), 3.58-3.65 (m, 2H, OCH2CH2OH), 3.7-3.82 (m, 4H, —CH2OCH2CH2OH), 3.97-4.04 (m, 2H, ArOCH2—), 6.56 (d, 2H, aromatic proton ortho to hydroxy), 6.78 (d, 2H, aromatic proton meta to hydroxy), 7.1-7.43 (m, 10H, aromatic protons)
4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenol (0.23 g, 0.689 mmol) was dissolved in tetrahydrofuran (3 ml) under nitrogen atmosphere. Sodium hydride (0.025 g, 1.03 mmol) was added to the solution and the mixture was stirred at room temperature for an hour. 2-(2-iodo-ethoxy)-tetrahydropyran (0.3 g, 1.17 mmol) was added and the mixture was refluxed for 2 hours. Additional portions of 2-(2-iodo-ethoxy)-tetrahydro-pyran (0.5 g, 2 mmol) were added to the mixture during seven hours. After cooling and adding water, THF was evaporated and the mixture was extracted three times with ethyl acetate. The organic phase was washed with 2 N aqueous sodium hydroxide and water, dried with sodium sulphate and evaporated to dryness. The residue (which is Compound (IV) where Pr is tetrahydropyranyl) was dissolved in ethanol and acidified with 2 N aqueous hydrogen chloride solution. The mixture was stirred at room temperature over night, evaporated and extracted with dichloromethane. After washing with water the organic phase was dried (Na2SO4) and evaporated. The residue was purified by flash chromatography with dichloromethane/methanol 9.5/0.5 as eluent. Yield 0.17 g, 59%.
Z-isomer, 1H NMR (CDCl3): 2.92 (t, 2H, ═CH2CH2Cl), 3.42 (t, 2H, ═CH2CH2Cl), 3.85-3.89 (m, 4H, OCH2CH2), 6.56 (d, 2H, aromatic proton ortho to hydroxy), 6.80 (d, 2H, aromatic proton meta to hydroxy), 7.1-7.43 (m, 10H, aromatic protons).
The compound was prepared by the same method as described in Example 4 using 2-(2-iodo-ethoxymethyl)-benzene as a reagent and removing the benzylic protecting group using the method described in Example (e) of U.S. Pat. No. 6,891,070 B2, herein incorporated by reference. Briefly, the removal is carried out under a nitrogen atmosphere, in the presence of Zn powder and acetyl chloride.
4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenol (0.5 g, 0.0015 mol), absolute ethanol (10 ml), potassium carbonate (0.62 g, 0.0045 mol) and ethyl bromo acetate (0.373 g, 0.00224 mol) are mixed under nitrogen atmosphere and refluxed for 2.5 hours. Then the hot mixture was filtered and the precipitate was washed with absolute ethanol. The filtrate was evaporated, extracted with ethyl acetate and washed with water. Ethyl acetate was dried (Na2SO4) and evaporated to dryness. Yield 260 mg, 52%. The product was used without further purification in the next reaction step.
1H NMR (CDCl3+ MeOH-d4): 1.25 (t, 3H, CH2CH3), 2.92 (t, 2H, ═CH2CH2Cl), 3.42 (t, 2H, ═CH2CH2Cl), 4.22 (q, 2H, OCH2CH3), 4.49 (s, 2H, ArOCH2—), 6.56 (d, 2H, aromatic proton ortho to hydroxy), 6.80 (d, 2H, aromatic proton meta to hydroxy), 7.1-7.43 (m, 10H, aromatic protons).
An alternative way to carry out the alkylation described in Example 6 is to replace absolute ethanol and potassium carbonate by sodium hydride and tetrahydrofuran. Preliminary experiments gave the product in high yield (90%) after a short reaction time (about 1 hour) at room temperature.
[4-(4-Chloro-1,2-diphenyl-but-1-enyl)-phenoxy]-acetic acid ethyl ester (Example 7) was dissolved in tetrahydrofuran at room temperature under nitrogen atmosphere. Lithium aluminium hydride was added to the solution in small portions until the reaction was complete. The reaction was quenched by adding saturated ammonium chloride solution to the mixture. The product was extracted into toluene, which was dried and evaporated in vacuo. The yield 100 mg, 43%.
1H NMR (CDCl3): 2.92 (t, 2H, ═CH2CH2Cl), 3.42 (t, 2H, ═CH2CH2Cl), 3.85-3.89 (m, 4H, OCH2CH2), 6.56 (d, 2H, aromatic proton ortho to hydroxy), 6.80 (d, 2H, aromatic proton meta to hydroxy), 7.1-7.43 (m, 10H, aromatic protons).
It will be appreciated that the methods of the present invention can be incorporated in the form of a variety of embodiments, only a few of which are disclosed herein. It will be apparent to one of ordinary skill in the art that other embodiments exist and do not depart from the spirit of the invention. Thus, the described embodiments are illustrative and should not be construed as restrictive.
This application is a Divisional Application of U.S. Ser. No. 12/030,420, filed Feb. 13, 2008, now U.S. Pat. No. 7,812,197, which is application claims priority to U.S. Provisional Patent Application No. 60/889,838 filed Feb. 14, 2007, all of which are incorporated herein by reference in their entirety.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4177121 | Ando et al. | Dec 1979 | A |
| 4656187 | Black et al. | Apr 1987 | A |
| 4696949 | Toivola et al. | Sep 1987 | A |
| 4894373 | Young | Jan 1990 | A |
| 4935243 | Borkan et al. | Jun 1990 | A |
| 4996225 | Toivola et al. | Feb 1991 | A |
| 5118667 | Adams et al. | Jun 1992 | A |
| 5189212 | Ruenitz | Feb 1993 | A |
| 5192525 | Yang et al. | Mar 1993 | A |
| 5196435 | Clemens et al. | Mar 1993 | A |
| 5352699 | Jackson | Oct 1994 | A |
| 5446203 | McNelis | Aug 1995 | A |
| 5470883 | Stromberg | Nov 1995 | A |
| 5491173 | Toivola et al. | Feb 1996 | A |
| 5567714 | Bruns | Oct 1996 | A |
| 5658931 | Bryant et al. | Aug 1997 | A |
| 5691355 | Bryant et al. | Nov 1997 | A |
| 5693674 | Bitonti | Dec 1997 | A |
| 5719136 | Chwalisz et al. | Feb 1998 | A |
| 5747059 | Korsgaard et al. | May 1998 | A |
| 5750576 | DeGregorio et al. | May 1998 | A |
| 5807899 | Bohlmann et al. | Sep 1998 | A |
| 5821254 | Sporn et al. | Oct 1998 | A |
| 5827892 | Loser et al. | Oct 1998 | A |
| 5852059 | Thompson | Dec 1998 | A |
| 5877219 | Willson | Mar 1999 | A |
| 5912273 | DeGregorio et al. | Jun 1999 | A |
| 6037379 | Harkonen et al. | Mar 2000 | A |
| 6245342 | Golz-Berner et al. | Jun 2001 | B1 |
| 6245352 | Arbuthnot et al. | Jun 2001 | B1 |
| 6245819 | Halonen et al. | Jun 2001 | B1 |
| 6525084 | Rasmussen et al. | Feb 2003 | B2 |
| 6576645 | Sodervall et al. | Jun 2003 | B1 |
| 6632447 | Steiner et al. | Oct 2003 | B1 |
| 6875775 | Sodervall et al. | Apr 2005 | B2 |
| 6984665 | Blom et al. | Jan 2006 | B2 |
| 7504530 | Sodervall et al. | Mar 2009 | B2 |
| 20010034340 | Pickar | Oct 2001 | A1 |
| 20040248989 | Santti et al. | Dec 2004 | A1 |
| 20050182143 | Anttila | Aug 2005 | A1 |
| 20050187302 | Blom | Aug 2005 | A1 |
| 20050215528 | Furuya et al. | Sep 2005 | A1 |
| 20070104742 | Lehtola et al. | May 2007 | A1 |
| 20070197664 | Steiner et al. | Aug 2007 | A1 |
| 20070203180 | Hoekstra et al. | Aug 2007 | A1 |
| 20080207956 | Sodervall et al. | Aug 2008 | A1 |
| Number | Date | Country |
|---|---|---|
| 0 095 875 | Dec 1983 | EP |
| 0 664 124 | Jul 1995 | EP |
| 0 779 808 | Aug 1999 | EP |
| 0 760 651 | Jul 2001 | EP |
| 1 125 582 | Aug 2001 | EP |
| WO 9206068 | Apr 1992 | WO |
| WO 9319746 | Oct 1993 | WO |
| WO 9526720 | Oct 1995 | WO |
| WO 9607402 | Mar 1996 | WO |
| WO 9635417 | Nov 1996 | WO |
| WO 9640616 | Dec 1996 | WO |
| WO 9732574 | Sep 1997 | WO |
| WO 9942427 | Aug 1999 | WO |
| WO 9963974 | Dec 1999 | WO |
| WO 0136360 | May 2001 | WO |
| WO 0154699 | Aug 2001 | WO |
| WO 0207718 | Jan 2002 | WO |
| WO 02090305 | Nov 2002 | WO |
| WO 03047504 | Jun 2003 | WO |
| WO 03103649 | Dec 2003 | WO |
| WO 2005079777 | Sep 2005 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20110015448 A1 | Jan 2011 | US |
| Number | Date | Country | |
|---|---|---|---|
| 60889838 | Feb 2007 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12030420 | Feb 2008 | US |
| Child | 12883680 | US |
