Patent Application
20090221837
The present invention relates to the process for the preparation of pure Anastrozole.
Aromatase is an enzyme, which effects aromatisation of ring A in the metabolic formation of various steroid hormones. Various cancers for example breast cancer are dependent upon circulating steroid hormones, which have an aromatic ring A. Such cancers can be treated by removing the source of ring A aromatised steroid hormones, for example by the combination of oophorectomy and adrenalectomy. An alternative way of obtaining the same effect is by administering a chemical compound, which inhibits the aromatisation of the steroid ring A.
Anastrozole is a non-steroidal antineoplastic, claimed to inhibit the aromatase (oestrogen synthase) activity. It is useful in the treatment of advanced breast cancer in postmenopausal women.
Synthesis of Anastrozole is reported in U.S. Pat. No. 4,935,437 and European Patent Application No. EP 0,296,749. In the above patents the synthesis of Anastrozole is started from intermediate 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1), which undergoes bromination to provide 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2) followed by condensation with 1,2,4-triazole (4) to form Anastrozole (5). (Scheme-1)
The major problem with the synthesis of Anastrozole is the formation of regioisomer impurity in the said process. The regioisomer (6), which forms in 10-20% during the reaction of 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2) with 1,2,4-triazole (4), is removed by the purification by crystallization from suitable solvents with a major loss in yield of desired product.
To overcome the formation of regioisomer (6), another synthetic route is reported in U.S. Pat. No. 4,935,437; in which intermediate (2) is reacted with 4-amino-1,2,4-triazole (7) to form quaternary ammonium salt (8), which further undergoes diazotisation reaction to give Anastrozole (5) free from any isomeric impurity (Scheme-2). This process avoids the formation of Anastrozole regioisomer (6), but possibilities of other impurities remain same, which arise from impure intermediate (2) contaminated with unreacted starting material (1) and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3). Thus the main objective of the present invention relates to an improved process for the preparation of pure Anastrozole (5) free from impurities arises due to impure intermediate (2) contaminated with unreacted starting material (1) and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3).
To avoid the formation of regioisomer (6) during the formation of Anastrozole (5); intermediate (2) is treated with 4-amino-1,2,4-triazole (7) to form quaternary ammonium salt (8), which further undergoes diazotisation reaction to give Anastrozole (5) free from any isomeric impurity.
The said process avoids the formation of Anastrozole regioisomer (6), but possibilities of other impurities still remain unaffected, which arise from impure intermediate (2) contaminated with unreacted starting material (1) and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3).
The present invention relates to an improved process for the preparation of pure Anastrozole (5) free from impurities arising due to impure intermediate (2) contaminated with unreacted starting material (1) and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3).
Intermediate (2) of more than 80% HPLC purity contaminated with dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3) less than 5% and unreacted starting material 2,2-(5-methyl-1,3-phenylene)-bis(2-methyl-propionitrile) (1) less than 15%, undergoes condensation with 4-amino-1,2,4-triazole (7) in a suitable solvent to give 4-Amino-1-[3,5-bis-(1-cyano-1-methylethyl)benzyl]-1H-[1,2,4]triazolium bromide (Q.A.-salt) (8) in good yield. Quaternary ammonium salt (Q.A.-salt) (8) on HPLC analysis shows excellent purity, but still contaminated with 2,2-(5-methyl-1,3-phenylene)-bis(2-methyl-propionitrile) (1) and unreacted 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2). However, HPLC analysis of mother liquor shows that majority of 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1) and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3) are being removed in mother liquor. These results reveal the separations of major part of above impurities in mother liquor during the filtration of Q.A.-salt, but still some extent of related impurities are observed in the HPLC analysis of Q.A.-salt.
Further the Q.A.-salt undergoes diazotisation reaction to give Anastrozole. During the said process, an acidic salt of Anastrozole is prepared in between the process and other impurities are removed by washing acidic Anastrozole salt with an organic solvent. The acidic Anastrozole salt on further basifying and isolation in a suitable solvent affords Anastrozole, which is further purified using organic solvents preferably isopropanol, ethyl acetate or mixture of solvents preferably cyclohexane/ethyl acetate, cyclohexane/isopropanol or a mixture of solvents with water. Thus another embodiment of the present invention relates to the process for the preparation of Anastrozole comprising:
During the formation of Q.A.-salt (8), on reaction of intermediate (2) with 4-amino-1,2,4-triazole (7), 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1) and dibrominated by-product (3) remain unreacted. HPLC analysis of mother liquor shows the presence of 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1) and dibrominated by-product (3) in mother liquor. However, some extents of these two impurities are also observed in the Q.A.-salt (8), which are removed by washing of acidic aqueous layer of Anastrozole with suitable organic solvent.
The present invention also relates to an improved and safe process for the preparation of 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2), which involves replacing hazardous chlorinated solvent with a safe and environmentally more friendly solvents as the reaction media. The preferred solvents for this purpose are selected from hydrocarbons, preferably aliphatic hydrocarbons, more preferably cyclic aliphatic hydrocarbons and most preferably cyclohexane. Thus another embodiment of the present invention relates to an improved process for the preparation of 3,5-bis-(1-cyano-1-methylethyl)benzylbromide of structural formula (2) comprising:
Accordingly, the present invention provides aprocess for the preparation of Anastrozole free from 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) of structural formula (1) and 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene of structural formula (3)
each of them preferably less than 0.1% and more preferably below quantitation limits, and all other known/unknown impurities less than 0.1% comprising:
Preferably, the organic solvent in employed in step (b) is a hydrocarbon, preferably, aromatic hydrocarbon and more preferably toluene.
In another preferred feature, the solvent empployed for extraction in step (c) comprises one or more water immiscible organic solvents.
In another preferred feature, said solvents employed in the purification of Anastrozole in step (d) are selected from alcohols, ketones, nitrites, esters, hydrocarbons and water independently or mixture thereof.
In another embodiment, the present invention provides an improved process for the preparation of 3,5-bis-(1-cyano-1-methylethyl)benzylbromide of structural formula (2) comprising:
In another preferred feature, said hydrocarbon employed in step (a) is preferably an aliphatic hydrocarbon and more preferably, a aliphatic cyclic hydrocarbon.
In another preferred feature, the said aliphatic cyclic hydrocarbon is cyclohexane.
In another preferred feature, the said brominating reagent used in operation (a) is preferably N-bromosuccinimide or 1,3-dibromo-5,5-dimethylhydantoin.
In another preferred feature, said solvent employed in said crystallization is an alcohol preferably, a C1-C10 and more preferably, methanol or isopropanol.
The present invention will now be described with reference to the following non-limiting examples which are merely for the purposes of illustrating the invention. It will be apparent to a person skilled in the art that various modifications may be possible within the present invention without departing from the scope thereof.
In a 5 L R. B. Flask, fitted with double surface condenser and thermometer pocket on a water bath cyclohexane (1.5 L), 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1) (50 g), 2,2-Azo-bis(isobutyronitrile) (AIBN) (2 g) and 1,3-dibromo-5,5-dimethylhydantoin (130 g) were charged at 25-35° C. The reaction mixture was heated at 80-85° C. with vigorous stirring for 4 hours. The reaction mass was cooled to 25-35° C. and washed with water (500 mL×2) followed by washing with 2% aqueous solution of sodium thiosulphate (500 mL). Cyclohexane layer was separated and distilled under vacuum at 50-55° C. to get residue, which was crystallised from cyclohexane (250 mL) and further dried at 55-60° C. for 3 hours, to get crude product 52 gm, which on crystallization from methanol gave product (37 gm). HPLC-purity shows 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2) as product >80%, contaminated with unreacted 2,2-(5-methyl-1,3-phenylene)-bis(2-methylpropionitrile) (1) <15% and dibrominated by-product 3,5-bis(1-cyano-1-methylethyl)-α,α-dibromotoluene (3) <5%.
Isopropanol (1.5 L), 3,5-bis-(1-cyano-1-methylethyl)benzylbromide (2) (100 g) and 4-amino-1,2,4-triazole (22.5 g) were charged in a flask at room temperature. The reaction mass was heated at 80-85° C. for next 5 hours. The reaction mass was further cooled down to room temperature and stirred for next one hour at 25-35° C. The precipitated solid QA-salt was filtered and washed with fresh isopropanol (100 mL×2). The Q.A.-salt was dried at 60-70° C. till LOD is less than 1.0%, giving solid product (74.4 g). m.p.: 198-200° C.
4-Amino-1-[3,5-bis-(1-cyano-1-methylethyl)benzyl]-1H-[1,2,4]triazolium bromide (8) (70 g) was dissolved in conc. HCl (280 mL) in a 5 L R.B. flask and cooled to −5° C. A solution of sodium nitrite (15 g) in water (70 mL) was slowly added to the reaction mixture at 0-5° C. in 4 hrs and the reaction mixture was stirred for one hour at 0-5° C. and further at 10-20° C. for next 3 hours. The reaction mixture was quenched by the addition of a solution of urea (4.5 g) in water (15 mL). Toluene (700 mL) was added to the reaction mixture and the heterogeneous solution was further cooled down to 0-5° C. The solution was basified by the addition of liquor ammonia (365 mL) slowly in 4 hours at 5-25° C. Organic layer was separated and further washed with water (200 mL). Aqueous layer was removed and a solution of conc. HCl (140 mL) in water (140 mL) was added to the organic layer slowly in 30 minutes at 25-30° C. and reaction mass was heated at 60-65° C. for 30 minutes. The lower aqueous layer (280-300 mL) containing product was collected in a conical flask maintaining at 50° C. The aqueous part was again washed with toluene (700 mL) at 60-65° C. for 30 minutes. The lower aqueous layer, containing product was charged in a separating funnel and again washed with fresh toluene (700 mL). The aqueous layer, containing product was transferred in a R.B. flask and ethyl acetate (350, mL) was added to it. The heterogeneous solution was cooled to 0-5° C. basified by the slow addition of liquor ammonia (280 mL) in 2-3 hours at 5-25° C. The solution was stirred for one hour at 25-35° C., and the upper organic layer (360-375 mL) containing product was separated and filtered through hyflow super cell bed. Solvent was distilled out below 50° C. under vacuum leaving approximately 100 mL ethyl acetate in the flask. The content of the flask was cooled down to 25-35° C. and cyclohexane (500 mL) was added to the solution slowly in 30 minutes. The precipitated solid product was filtered and washed with fresh cyclohexane (20 mL×2). The product was dried at 45-50° C. till LOD was less than 1.0% to get Anastrozole (44 g). HPLC-purity: not less than 98%.
In a R.B. flask Anastrozole (32 g) from example-3 was dissolved completely in ethyl acetate (64 mL) at 35-40° C. The solution was cooled down to 25-35° C. and cyclohexane (320 mL) was added slowly to the solution under stirring in 1 hour. The solution was further stirred at 25-35° C. for 2 hours, and the precipitated solid product was filtered, washed with fresh cyclohexane (15 mL×2) at 25-35° C. The solid product was dried at 50° C., till LOD was less than 0.5%. Weight of dry Anastrozole: 30 g. HPLC-purity: not less than 99.5%.
Anastrozole (110 g) from example-3 was dissolved in isopropanol (330 mL) at 45-50° C. The solution was cooled down to 25-35° C. and cyclohexane (330 mL) was added drop wise in 30 minutes. The solution was stirred at 25-35° C. for 2 hours; the precipitated solid product was filtered and washed with fresh cyclohexane (30 mL×2) and dried at 50° C. to get 92 g of pure Anastrozole. HPLC-purity: not less than 99.5%.
Anastrozole (5 g) from example-3 was dissolved in ethanol (10 mL) at 45-50° C. The solution was cooled down to 25-35° C. and cyclohexane (50 mL) was added drop wise in 30 minutes. The solution was stirred at 25-35° C. for 2 hours; the precipitated solid product was filtered and washed with fresh cyclohexane (5 mL×2) and dried at 50° C. to get 4.0 g of pure Anastrozole. HPLC-purity: not less than 99.5%.
Anastrozole (5 g) from example-3 was dissolved in isopropanol (20 mL) at 50-55° C. The solution was cooled down to 5-10° C. and stirred for 2 hours; the precipitated solid product was filtered and washed with chilled fresh isopropanol (5 mL) and dried at 50° C. to get 4.5 g of pure Anastrozole. HPLC-purity: not less than 99.5%.
Anastrozole (5 g) from example-3 was dissolved in isopropanol (5 mL) and water (20 mL) at 65-70° C. The solution was cooled down to 25-35° C. and stirred for 1 hour; the precipitated solid product was filtered and dried at 50° C. to get 4.5 g of pure Anastrozole. HPLC-purity: not less than 99.5%.
Anastrozdle (5 g) from example-3 was dissolved in ethanol (5 mL) and water (40 mL) at 50-55° C. The solution was cooled down to 25-35° C. and stirred for 1 hour; the precipitated solid product was filtered and dried at 50° C. to get 4.5 g of pure Anastrozole. HPLC-purity: not less than 99.5%.
Anastrozole (5 g) from example-3 was dissolved in methanol (5 mL) and water (20 mL) at 50-55° C. The solution was cooled down to 25-35° C. stirred for 2 hours; the precipitated solid product was filtered and dried at 50° C. to get 4.5 g of pure Anastrozole. IPLC-purity: not less than 99.5%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1216-MUM-2005 | Sep 2005 | IN | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IN2006/000336 | 9/4/2006 | WO | 00 | 4/16/2009 |
