Patent Application
20100087661
The invention deals with a new method of preparation of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1
which is used for the production of 2-(4-hydroxyphenyl)-1-[4-(2-azepan-1-yl-ethoxy)benzyl]-3-methyl-1H-indol-5-ol (bazedoxifen) of formula 2.
Bazedoxifen is an agonist of oestrogen; it is used within hormone substitution therapy for prevention of bone tissue loss, replacement of oestrogen and prevention of heart and vein diseases in post-menopausal women.
In literature two analogous methods for the preparation of bazedoxifen have been found—see Scheme 1. The methods differ in the protective group (PG—methyl, benzyl), in the way of preparation and connection of the chain to the nitrogen of the indole heterocycle and the way of removal of the protective group.
5-Methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole of formula 3a is prepared by the Bischler method (J. Med. Chem. 1984, 27, 1439-1447; WO 9603375) from 2-bromo-4′-methoxypropiophenone of formula 5 and p-anisidine of formula 6 in o-xylene in the presence of N,N-dimethylaniline. 2-Bromo-4′-methoxypropiophenone of formula 5 is obtained by bromination of 4-methoxypropiophenone of formula 4 with bromine in acetic acid (WO 9603375), see Scheme 2.
The total yield of the two-stage synthesis is 22%.
5-Benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 is also prepared by the Bischler method from 2-bromo-4′-benzyloxypropiophenone of formula 8 and 4-benzyloxyaniline hydrochloride of formula 9 in N,N-dimethylformamide (EP 0802183). 2-Bromo-4′-benzyloxypropiophenone of formula 8 is obtained by bromination of 4-benzyloxypropiophenone of formula 7 with bromine in acetic acid. The total yield of the two-stage synthesis (see Scheme 3) is 47%.
Patent application no. WO 9919293 mentions carrying the second stage out in toluene with N,N-diisopropylethylamine under reflux; however, without any further specification in the examples or reference to literature.
Verification syntheses have shown that with the above mentioned preparation methods the compound of formula 1 cannot be obtained with a sufficiently high yield and, especially, in sufficient purity.
In reproducing the process in accordance with patent no. EP 802183 (Scheme 4) it has been found out that during this synthesis high quantities of undesired substances are generated.
Isolation of the compound of formula 1 prepared this way is considerably complicated and its purification significantly reduces the yield of the synthesis.
In carrying the reaction out in accordance with the patent application no. WO 9919293, which describes preparation of the compound of formula 1 in the environment of toluene and N,N-diisopropylethylamine under simultaneous removal of water by azeotropic distillation, it has been found out that the reaction time takes several tens of hour. During this time already a substantial amount of secondary substances are generated that reduce the yield and quality of the product.
For this reason there was an effort to find a more efficient way of synthesis, the result of which is the new method for the preparation of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1, which consists the object of the present invention.
The invention deals with a new method for the preparation of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1, which is based on isolation of the intermediate N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10. This intermediate product is preferably obtained by reaction of 4-benzyloxyaniline or its salt with a substance of formula 11
wherein LG is a leaving group, e.g. Cl, Br, I, alkylsufonyl or arylsulfonyl.
The preparation process comprises
a) Reaction of 2-bromo-4′-benzyloxypropiophenone of formula 8 with p-benzyloxyaniline hydrochloride of formula 9, the reaction being carried out in the environment of an organic solvent from the group of C1 to C4 alcohols, toluene, acetone, methyltetrahydrofuran and in the presence of an inorganic or organic base from the group including sodium carbonate, potassium carbonate DIPEA and triethylamine;
b) Isolation of N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10 in the solid state;
c) Cyclization of N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10 by reaction with p-benzyloxyaniline hydrochloride of formula 9 in the environment of a suitable organic solvent from the group of C1 to C4 alcohols, toluene, acetone, methyltetrahydrofuran to give 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 in the solid state.
It has been found out that it is advantageous to carry out synthesis of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 in 2 stages with isolation of the intermediate of formula 10 in accordance with Scheme 7.
In the first stage the starting compounds 8 and 9 are reacted in the environment of an organic solvent from the group of C1 to C4 alcohols, toluene, ketones, methyltetrahydrofuran, preferably ethanol, and an inorganic or organic base from the group including sodium carbonate, triethylamine and DIPEA, preferably triethylamine, at the reflux temperature for 4-6 hours. In this manner a suspension of the intermediate 10 and possibly inorganic salts (corresponding to the base used) is formed after several hours. The intermediate is isolated by filtration. The product yield is 81 to 100%.
The product can be re-crystallized by dissolution in a mixture of a polar and non-polar solvent (ethyl acetate-ethanol, toluene-methanol, THF-methanol).
In the second stage N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10 is suspended, together with p-benzyloxyaniline hydrochloride of formula 9 (molar ratio 1:20 to 1:1, preferably 1:5 with respect to the compound of formula 10), in an organic solvent from the group of C1-C4 alcohols, toluene, and methyltetrahydrofuran, preferably ethanol, and the mixture is heated up in a pressure vessel under inert atmosphere to 100 to 120° C. After several hours (4 to 5) the reaction mixture is cooled to the laboratory temperature. The crystallized product 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 is filtered, washed with ethanol and optionally re-crystallized from a mixture of a polar and non-polar solvent (ethyl acetate-ethanol, toluene-methanol, THF-methanol). The yield of the reaction is 75 to 80%.
It is advantageous that the starting aniline of formula 9 can be obtained from the mother liquor, after concentrating and stirring the concentrated matter up in ethyl acetate, back with nearly 100% yield.
This original method is based on the preparation and isolation of a new substance, the intermediate N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10. The main advantages of the method include a higher yield (60 to 75%) as compared to the published methods (35 to 53%), easy isolation of the intermediate N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone of formula 10 as well as the final product 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 by filtration directly from the reaction mixture without using any additional chemicals and, above all, the achievement of a high quality of the crude product already (HPLC 98 to 100%). Another advantage is that the starting benzyloxyaniline hydrochloride of formula 9, used for the cyclization reaction, is not consumed and can be obtained from the mother liquors after isolation of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole of formula 1 in a quantitative yield.
The invention is described in more detail in the following examples.
1) α-Bromo-4-benzyloxypropiophenone (20 g; 62.7 mmol), 4-benzyloxyaniline (16 g; 67.9 mmol) and triethylamine (19 ml; 136.4 mmol) were suspended in 250 ml of toluene and the mixture was refluxed for 5 hours. Then, the reaction mixture was filtered and concentrated to ca. ⅓ of the volume. Ethanol (80 ml) was added to the concentrated matter and the mixture was cooled to 5° C. With filtration 19.2 g (71%) of a grey product, N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (10), were obtained with the melting temperature of 124.5-126° C.
2) α-Bromo-4-benzyloxypropiophenone (26 g; 81.5 mmol), 4-benzyloxyaniline (23 g; 97.8 mmol) and sodium carbonate (20.7 g; 196 mmol) were suspended in 300 ml of ethanol and the mixture was refluxed for 5 hours. During said period the product precipitates. After cooling of the reaction mixture a mixture of the salts (NaBr, NaCl, sodium carbonate) and the crystallized product was isolated by filtration. The isolated mixture of substances was dissolved in a toluene-water mixture. After separation of the aqueous phase the organic phase was concentrated. Ethanol was added to the concentrated residue. The precipitated slightly yellowish crystalline product was isolated by filtration and washed with ethanol. 30.2 g (85%) of N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (10) were obtained. Melting temperature 126.0-127.1° C.
3) α-Bromo-4-benzyloxypropiophenone (16.1 g; 50.5 mmol), 4-benzyloxyaniline (14.2 g; 60.1 mmol) and triethylamine (16.1 ml; 115.6 mmol) were suspended in 130 ml of ethanol and the mixture was refluxed for 5 hours. Then, being stirred the mixture was cooled to the laboratory temperature within 1 hour. The filtered product was washed with ethanol and dried. 21.9 g (99.5%) of N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (10) were obtained. Melting temperature 122.6-125.4° C.
The crude product, N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (10) (15.4 g) was dissolved in toluene (40 ml) by heating up to 60° C. The solution was filtered and ethanol (40 ml) was added to the filtrate. After cooling to 10 to 15° C. 13.8 g (89.6%) of a white product with the melting temperature of 126.1-127.1° C. were obtained. 1H-NMR (DMSO) δ 8.10 (d, 2H); 7.3-7.5 (m, 12H); 7.19 (d, 2H); 7.06 (d, 2H); 5.5 (q, 1H); 5.24 (s, 2H); 5.08 (s, 2H); 1.48 (d, 3H).
The X-ray difractogram of the obtained product is shown in
1) The starting N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (22) (30.4 g; 69.7 mmol) and 4-benzyloxyaniline hydrochloride (3.3 g; 13.9 mmol) were suspended in ethanol (380 ml) and the mixture was heated to 110-115° C. under an inert atmosphere in a pressure vessel. After 5 hours the heating was disconnected and the reaction mixture was stirred overnight. The crystallized white product was filtered and washed with ethanol. 23.3 g (79%) of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole (3b) with the melting temperature of 152.4-153.4° C. were obtained. 1H-NMR (DMSO) δ 10.65 (s, 1H); 7.55 (d, 2H); 7.50 (d, 4H); 7.30-7.45 (m, 6H); 7.21(d, 1H); 7.10 (d, 2H); 7.10 (d, 1H); 6.91 (dd, 1H); 5.16 (s, 2H); 5.11 (s, 2H); 2.33 (s, 3H). MS eI m/z 419.
2) The starting N-(4-benzyloxyphenyl)-α-amino-4-benzyloxypropiophenone (22) (30.4 g; 69.7 mmol) and 4-benzyloxyaniline hydrochloride (3.3 g; 13.9 mmol) were suspended in propan-2-ol (380 ml) and the mixture was heated up to 110-115° C. under an inert atmosphere in a pressure vessel. After 5 hours the heating was disconnected and the reaction mixture was stirred overnight. The crystallized beige product was filtered and washed with a small quantity of propan-2-ol. 24.2 g (82%) of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-methyl-1H-indole (3b) with the melting temperature of 152.0-153.2° C. were obtained.
The mother liquors after the filtration were concentrated and the concentrated matter was stirred up in ethyl acetate (30 ml). The precipitated crystalline substance was filtered. 3.3 g of beige 4-benzyloxyaniline hydrochloride were obtained.
| Number | Date | Country | Kind |
|---|---|---|---|
| PV 2007-110 | Feb 2007 | CZ | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CZ08/00016 | 2/11/2007 | WO | 00 | 8/11/2009 |
