Title of Invention

PROCESS FOR THE PREPARATION OF A SUBSTITUTED BENZENE DICARBOXYLIC ACID DICHLORIDE

Abstract

(ST) Abstract The present invention refers to a process for the preparation of S-(-)-5-"[2-( acetyXoxy)-l-oxopropy]-amino] -2,4,6-triiodo1 ,3-benzenedicarboxyllc acid dichloride of formula (I) comprising the reaction between S-(-)-[2- (aoetyloxy)] propionic acid chloride and 5-amino-2,4t 6-triiodo-1,3- benzenedioarboxylic acid dichioride, in an aprotic dipolar solvent and in presence of a halogenhydrio acid and recovering the said compound from the reaction mixture by know means. PRICE : THIRTY RUPEES

Full Text

This invention refers to a new process for the synthesis of S-5-[[2-(acetyloxy)-1-oxopropyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride of formula (I). The compound of formula (I) has been previously described in patent GB 1472050 and used as intermediate for the synthesis of S-N,N'-bis[2-hydroxy-l-(hydroxyme-thyl)ethyl]-5-[(2-hydroxy-l-oxopropyl)amino]-2,4,6-tri-iodol,3-benzenedicarboxamide, from now on called Compound A. The synthesis of the compound of formula (I) described in the above mentioned patent foresees the following reaction as in Scheme 1. The reaction of 5-amino-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride (compound of formula (II)) is carried out, according to GB 1472050, with 2.5 equivalents of S-(- )-[2-(acetyloxy)]propionic acid chloride, in dimethylacetamide at 3-5°C. Recently, patent application GB 2271990 has been published, which describes a process for the preparation of compound (I) characterized by the use, in the reaction of Scheme 1, of a Lewis acid in catalytic amounts. According to the authors, the improvement brought by the invention lies in the quantitative conversions. The reaction solvent can be varied thus avoiding the drawbacks deriving from the removal of dimethylacetamide. As previously cited, Compound A is a product containing a chiral centre and whose pharmacopoeia standards (for instance USP XXV; FU IX ed.) indicate a specific minimum rotatory optical power ranging between [a]436 = -4.6° and -5.2° (c = 40, H20). It has been found, and this is one of the aspects of this invention, that the reaction of the Scheme 1 when carried out in dimethylacetamide or in another aprotic dipolar solvent, in presence of an halogenhydric acid, leads to a reaction mixture containing an optical and chemical pure final product. Furthermore, the present invention refers to a in¬dustrially convenient process for the purification of this reaction mixture, which leads to the pure product of formula (I) in high yield and with a specific rota¬tory optical power ranging between [a]D = -13.7 and -14.7° (c = 10, CH3CN) and with a chemical purity better than 99%. Said product, used as intermediate in the synthesis of Compound A, leads to a contrast agent which meets the pharmacopoeia standards and particularly those referring to specific rotatory optical power. Therefore, the scope of this invention is a process for the preparation of the compound of formula (I)/ which comprises the reaction between S-(-)-[2-(acetyloxy)]propionic acid chloride with the compound of formula (II), 5-amino-2,4,6-triiodo-l,3-benzenedicar-boxylic acid dichloride, in an aprotic dipolar solvent and in presence of a halogenhydric acid. In a preferred embodiment of the invention the aprotic dipolar solvent is selected from the group con¬sisting of N,N-dimethylacetamide, N,N-dimethylformamide and N-methyl-2-pyrrolidone, preferably N,N-dime-thylacetamide. Particularly preferred are the conditions of reac¬tion, in which the halogenhydric acid is added as an anhydrous gas in a 0.1:3 molar ratio for the product of formula (II). Equally preferred are the conditions of reaction under which the amount of halogenhydric acid is added as a salt of the above cited aprotic dipolar solvents. Par¬ticularly preferred is the dimethylacetamide hydrochlo¬ride. Equally preferred are the conditions of reaction, under which the temperature ranges between 0 and 40°C. This invention also refers to the process for the purification and isolation of S-5-[[2-(acetyloxy)-l-oxo-propyl]amino]-2,4, 6-triiodo-l,3-benzenedicarboxylie acid dichloride coming from the reaction of formation of the same. It has been found that the dilution of the reaction mix¬ture, containing the final product and the aprotic dipo¬lar solvent, with a solvent selected from the group con¬sisting of: acetic acid esters with linear or branched (C3-C5) alcohols; secondary or tertiary alcohols, linear or branched (C3-C5); mono-, di- or polychloro (C1-C4) alkanes, followed by addition of water allows the iso¬lation of the desired product with excellent yield, the removal of the aprotic dipolar solvent in an easy and complete way, and gives a product which has all the ne¬cessary chemical-physical characteristics to carry out the synthesis of Compound A in accordance with pharmaco¬poeia standards. This invention also refers to the process of puri¬fication and isolation of S-(-)-5-[[2-(acetyloxy)-l-oxo-propyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride, comprising the following steps: the dilution of the reaction mixture with acetic acid esters with linear or branched (C3-C5) al- conois or mono-, cu- or polycnioro (C1-C4) alkanes in a ratio between the dilution solvent and the aprotic dipolar solvent of 0.3:1 to 2.5:1 w/w; the extraction of the aprotic dipolar solvent with water in a ratio of water to the dilution solvent ranging from 0.5:1 to 4:1 w/w; the precipitation of the product with water. Particularly preferred are the solvents selected from propyl acetate, n-butyl acetate and methylchloro-form. It has been surprisingly found that the purifica¬tion of the reaction mixture can be advantageously car¬ried out by using an alternative method based on the use of a continuous extractor, fed by the same solvent used for the dilution of the reaction mixture and with water to the two ends and with the reaction mixture on an in¬termediate plate. The product is isolated by concentra¬tion of the solvent phase. Also in this case the product meets the desired chemical-physical standards of purity. As far as the use of secondary or tertiary (C^-Cg) linear or branched alcohols is concerned, the dilution can be performed either through the addition of the se¬lected solvent to the reaction mixture, or by adding the reaction mixture to the hydroalcoholic solution contai¬ning the selected alcohol, always in a ratio of dilution solvent to the aprotic dipolar solvent present in the reaction mixture ranging from 0 to 1.5 w/w, preferably in a ratio ranging from 0.3 to 0.6 w/w. Accordingly the present invention provides a process lor the preparation of S-(-)-5£ [2-(acetyloxy)-1-oxopropyl] aminq]-2,4,6-triipdo-1,3-benzenedicarbdxylic acid dichloride of formula (I) comprising the reaction between S-(-)-[2-(acetyloxy£]propionic acid chloride and 5-amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid dichloride, in an aprotic dipolar solvent in presence of a halogenhydric acid and recovering the compound of formula I from the reaction mixture by known methods. The following examples of the practice of the present invention are meant to be illustrative and are in no way limiting the scope of the invention. EXAMPLE 1 (S)-5-[[2-(acetyloxy)-l-oxopropyl]amino]-2,4,6-triiodo-1,3-benzenedicarboxylic acid dichloride. A) S-(-)-[2-{acetyloxy)]propionic acid sodium salt 560 g of S-(-)lactic acid sodium salt are dissolved in 1.5 kg of acetic acid. 180 g of HC1 (35-38% w/w) and 650 g of acetic anhydride are added with stirring without exceeding a temperature of 40°C. The solution is cooled to 20°C and 20 g of anhydrous sodium acetate are added with stirring for 30 min. The resulting suspension is filtered trough celite and the filter is washed with 50 g of acetic acid. The filtrate is concentrated by di¬stillation under vacuum of a mixture formed by acetic acid-acetic anhydride (5-12% anhydride). The concen¬trate, corresponding to the desired product, is used as such in the successive step. B) S-(-)-[2-(acetyloxy)]propionic acid chloride 640 g of technical S0C12 are dropwise added to the concentrate obtained through step A), at a temperature of 80"C by keeping during this phase a temperature of 65-70°C. At the end of the addition the exceeding SOCl2 is eliminated via concentration under vacuum. The desi¬red product is distilled at a temperature of 45-70"C and at a pressure of 11-15 mmHg. 677 g of said product are obtained. Yield: 90% Gas-chromatography: 99.5% [aP = -35.8° (on the product) 1H-NMR, 13C-NMR, IR and MS spectra are consistent with the structure. C) 5-amino-l,3-benzenedicarboxylic acid 325 g 5-nitro-l,3-benzenedicarboxylic acid (product available on the market) are loaded into a reactor with 2.8 1 of water. It is heated to 60-70°C and the starting product dissolved by addition of 410 g of 30% NaOH. Then 10 g of charcoal are added; the slurry is filtered and the filter is washed with 200 ml of water. 8 g of Pd/C 5% (product available on the market ) are then loaded and conditioned with approx. 0.01 m2 ni¬trogen. 0.1 m3 hydrogen are added under a pressure of 30 kPa. The temperature spontaneously reaches 50°C and is kept by cooling. When the hydrogen consumption stops, the solution is kept under pressure for 1 h and then the residual hydrogen is removed by washing with 0.02 m3 of nitrogen. The suspension is filtered and the filter wa¬shed with 100 ml of water giving approx. 3.85 kg of so¬lution containing 5-amino-l,3-benzenedicarboxylic acid sodium salt. D) 5-amino-2,4,6-triiodo-l,3-benzenedicarboxylic acid In a reactor loaded with 2.75 1 of water, are added in sequence 0.08 kg of HCl (34% w/w), 3.85 kg of solu¬tion of 5-amino-l,3-benzenedicarboxylic acid sodium salt coming from the previous reaction and 375 g of H2SO4 (1:1 aqueous solution). The content is heated to 70°C, and during 3 hours 1.35 kg of a solution of ICl in HCl (44.5% iodine, molar ratio IC1:HC1=1:1) (product availa¬ble on the market) is added. When the addition is com¬plete the solution is heated to 90°C and the temperature kept for 6h. Then the content is cooled to 60°C and transferred to another reactor, where it is cooled to 30°C. The slurry is decolourised by adding 45 g of so¬dium bisulfite under stirring, then centrifuged and the product washed with 0.3 kg of water thus giving 935 g of the desired wet product. After drying, 830 g of the de¬sired product are obtained. Total yield of the two steps (on the anhydrous product): 95.0% Water content: 2% Potentiometric assay: 99.3% 1H-NMR, 13C-NMR, IR and MS spectra are consistent with the structure. E) 5-amino-2/4,6-triiodo-l/3-benzenedicarboxylic acid dichloride A mixture of 1.2 kg of compound D), 6 g of quino-line and 970 g of dodecane is heated at 65-70°C, with stirring in a nitrogen atmosphere. Then in 2h, 500-600 g of a mixture of SOC12/10% n-dodecane are added and then, in 4-6 h, 1 kg of S0C12 is added keeping the temperature between 65 and 70°C. When the addition is complete the content is heated at 80-85"C in 2h keeping the tempera¬ture for 6 h, to complete the reaction. Then the content under vacuum is cooled to 40-50 °C/and the temperature is kept to 80- 85°C with stirring, distilling a SOC12/10% n-dodecane mixture, which can be re-used. The pressure is taken to normal values through ni¬trogen, the content is cooled to a temperature of less than 55°C and always under' nitrogen atmosphere and with stirring, 1.3 kg of diethylenglycol dimethyl ether (diglyme) are added, keeping the temperature between 40 and 50°C. Then 280-240 g of NaOH are added (13-15% aqueous solution), while the temperature increases to approx. 60°C with a resulting final pH of 2.5-3. 300 g of water are added and pH is adjusted to 6 by adding 690-590 g of NaOH (13-15% aqueous solution); the mixture is then di¬luted with 150-180 g of water; at a temperature of 30oC. The suspension is filtered under nitrogen atmo¬sphere and the wet product washed with water. The pro¬duct is dried at 50-65°C, thus giving 1.237 kg of the desired product. Yield on anhydrous product: 95.6% Water content: 1% HPLC: 98.5% Stationary phase: column E. Merck LichrospherS) RP-18 5 urn 4 mm x 12.5 cm Mobile phase gradient elution A = water B = CH3CN min % B 0 60 3 60 12 80 19 80 20 60 Flow: 1.2 ml min-1 Temperature: 30°C UV detection: 240 nm 1H-NMR, 13C-NMR, IR and MS spectra are consistent with the structure. F) (S)-5-[[2-(acetyloxy)-1-oxopropy1]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride. 700 g of compound (E) are dissolved, at room tempe¬rature and with stirring, in 1 kg of dimethylacetamide and after cooling at 15°C, 15 g of HC1/ % are added. Then 288 g of compound B) are added in 4 h and the tem¬perature is kept between 8-15°C. The reaction terminates after keeping the solution for 30-40 h at a temperature of 6-15°C. 488 g of n-butylacetate and 1.28 kg of water are added to the reaction mixture with stirring in 5 min. Then the stirring is stopped for 15 minutes to separate the phases. The lower organic phase is formed by n-butyl acetate, final product and a small amount of dimethyla¬cetamide. After separation, the pH is adjusted at 4 by adding 450 g of 5% NaHC03 solution. Then 405 g of water are added with stirring obtaining a suspension which is filtered. The wet product is washed with 42.5 g of n-butyl acetate and with 600 g of water in two parts. The same operations are performed on the two remaining parts of the organic phase. The wet final product is dried at a temperature of 55°C, thus giving 755 g of the desired product. Yield on anhydrous product: 90.0% Water content: 1% [aJD = -14.2° (c = 10, CHoCN) 20 ° HPLC: 99.2% Stationary phase: column E. Merck LichrospherS)RP-18 5 pm 4 mm x 12.5 cm Mobile phase: gradient elution A = water B = CH3CN min % B 0 45 3 45 9.5 45 15 100 17 45 Flow: 1.0 ml min-1 Temperature: 30°C UV detection: 245 nm ^H-NMR, 13C-NMR, IR and MS spectra are consistent with the structure. EXAMPLE 2 Preparation of S-(-)-5-[[2-(acetyloxy)-l-oxopropyl]-amino]-2,4,6-triiodo-l/3-benzenedicarboxylic acid di-chloride in presence of dimethylacetamide hydrochloride (DMAC.HC1) 362 g of S-(-)-[2-(acetyloxy)]propionic acid chlo¬ride are dissolved, at a temperature of 15-17°C and with stirring, into 657 g of dimethylacetamide (DMAC) and 31 g of DMAC.HC1. Then a solution of 894 g of 5-amino-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride in 657 g of DMAC is added to the previous solution in 2h while keeping the temperature at 17°C. The reaction is completed after 20 h at the temperature of 17°C. 1300 g of n-butyl acetate are added and most of DMAC hydrochloride precipitates. The hydrochloride is removed through filtration. The extraction and washing operations are carried out in a 45-mm- diameter continuous extraction column equipped with rotating and pulsing plates (LABORTEC TK 40/15), fed as follows: plate flow rate total quantity plate 1 (bottom) n-butylacetate 4.7 1/h 7 kg plate 5 solution containing the product 2.3 1/h plate 13 K2C03 23%w/w solution 1.2 1/h 0.48 kg plate 15 (head) washing water 0.9 1/h 1.4 kg The solutions are fed by 3 dosing impulse-pumps PROMINENT and one peristaltic pump WATSON MARLOW 503U with con 3.2-mm tubing (for n-butylacetate). The pulsation and rotation rate are set at 60% and 20%. The area of the cross section of the extractor is approx. 16 cm2, which is partly occupied by the stirring system; the average free section is equal to 10 cm2. The extraction takes Ih and 30 min at a temperature lower than 30 °C, keeping n-butylacetate as continuous phase. The final organic phase is concentrated by di¬ stilling first heterogeneous azeotropic mixture H20/n- butylacetate at 20 Torr and at 27°C and then only the organic solvent at 35°C. In the final step of the con¬ centration the precipitation of the desired product oc¬ curs. After cooling, the product is filtered. After drying 925 g of the desired product are obtained. Yield on anhydrous product: 87% HPLC: 99.0% Chemical-physical characteristics are consistent with those previously described. EXAMPLE 3 Alternative purification of S-(-)-5-[[2-(acetyloxy)-l- oxopropyl]amino]2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride. 680 g of S-5-[[2-(acetyloxy)-l-oxopropyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid solution (prepared according to EXAMPLE 1) are diluted with 550 ml of CH3CCI3. After 15 min stirring at room temperature the solution is cooled at 17-18"C, and the pH is adju¬sted at 6-6.2 by adding 30% NaOH solution, keeping a temperature between 20-25°C. The reaction mixture, which contains NaCl, is diluted with 500 ml of water and kept under stirring for 30 min. The two phases are separated and the organic phase is poured into water at room tem¬perature under stirring with a resulting precipitation of the product. The solution is kept with stirring for 1 h at 20-23°C and then is filtered under pressure washing first with CH3CCI3 and then with water. 267 g of the de¬sired product are obtained. Isolation yield: 95% The characteristics are consistent with those pre¬viously described. EXAMPLE 4 Alternative purification of S-(-)-5-[[2-(acetyloxy)-l-oxopropyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride. 680 g of solution of S-5-[[2-(acetyloxy)-l-oxo-propyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic (prepared according to EXAMPLE 1) are diluted with 256 g of tBuOH. 1040 g of 7% NaOH solution are dropwise added at 30'C to pH 4.5-5.5. When the addition terminates the slurry is kept for 1 h under stirring by controlling the pH. The solid is filtered and washed with water. 256 g of the desired product are obtained. Isolation yield: 89.0% Chemical-physical characteristics are consistent with those previously described. EXAMPLE 5 Alternative purification of S-(-)-5-[[2-(acetyloxy)-l- oxopropyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic acid dichloride. 680 g of S-5-[[2-(acetyloxy)-l-oxopropyl]amino]-2,4,6-triiodo-l,3-benzenedicarboxylic solution (prepared according to EXAMPLE 1) are dropwise added to a hydroal-coholic solution of 496.4 g 30%wt of tert-butanol at a temperature of 20-40"C. Simultaneously approx. 612 g of 7% NaOH are added, to keep the pH between 3.5-5.5. When the dropping terminates the slurry is kept un¬der stirring at pH 3.5-4.5 for lh. The solid is filte¬red, and washed with water. 271 g of the desired product are obtained. Isolation yield: 95% Chemical-physical characteristics are consistent with those previously described. EXAMPLE 6 Following the method of EXAMPLE 4, tBuOH is substituted with 2-BuOH giving 241 g of the desired product. Isolation yield: 85.0% Chemical-physical characteristics are consistent with those previously described. We claim: 1. A process for the preparation oi S-(-)-5-r [2-Cacetyloxy)l-oxopropyl} aminq2,-2,4,6-triipdo-1,3-benze-nedicarboxylic acid dichloride oi formula (I) comprising the reaction between S-(-)-|2-(acetyloxy)] propionic acid chloride and 5-amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid dichloride, in an aprotic dipolar solvent in presence of a halogenhydric acid and recovering the compound of formula I from the reaction mixture by known methods. 2. The process as claimed in claim 1, wherein the halogenhydric acid is added as gas to the solution of 5-amino-2, 4,6-triiodo-1,3-benzenedicarboxylic acid dichloride before adding S-(-)-{2-(acetyloxy]propionic acid chloride. 3. The process as claimed is claim 3 wherein the added halogenhydric said is hydrochloric said. 4. Tha process as claimh in claim 3, wherein hydrochloric acid ia added ad in gaeousform in a solar ratio of 0.1;3 with respect to the substituted beazenedicarboxylic acid dichloride. 5. The process as claimed in any one of the claims from 1 to 4, wherein the apretic dipolar solvent is an organic solvent selected from a group consisting of N-N-dimethylacetanide and N-methyl-2-pyrolidineas, preferably the N-N-dimethyl acetamide dimethylasetamide. jj 9 The process as claimed in claim 6,wherein said hydrochloride of dimethylacatanida ia addad in a solar ratio of 0.1 to 3 with respect to tha aubatitutad bensane dicarboxylic acid dishloride. 8. The process aa claimed in claim1, wherein the reaction temperature ranges between 0 and 40C.

Documents:

861-mas-1996 abstract.pdf

861-mas-1996 claims.pdf

861-mas-1996 correspondence -others.pdf

861-mas-1996 correspondence -po.pdf

861-mas-1996 description (complete).pdf

861-mas-1996 form-2.pdf

861-mas-1996 form-26.pdf

861-mas-1996 form-4.pdf

861-mas-1996 form-8.pdf

861-mas-1996 others.pdf

861-mas-1996 petition.pdf