Method for preparing S-Bz-MAG3 as a precursor of contrast media

Abstract

The present invention provides a method for preparing S-Bz-MAG3 as a precursor of contrast media. Thioglycolic acid and benzoyl chloride are taken for the thiol protection reaction. Next, N,N′-dicyclohexylcarbodiimide and N-hydroxysuccinimide are converted to corresponding ester compounds. The corresponding ester compounds then react with triglycine by amide bonding reaction. The product of the reaction is recrystallized using acetone, filtered, and finally flushed using flushing agent to give the final product. This is a bifunctional chelator and can be bridged with 99mTc and 186/188Re effectively and applied to nuclear medicine imaging and tumor radiotherapy. By taking advantage of fewer synthesis steps and ease of operations, complicated separation and purification reactions can be reduced and thus achieving highly productivity of S-Bz-MAG3.

Claims

1. A method for preparing S-Bz-MAG3 as a precursor of contrast media, comprising steps of: taking thioglycolic acid and benzoyl chloride and stirring for 2 hours at room temperature for performing a thiol protection reaction and producing a first product; using concentrated hydrochloric acid to adjust pH value of said first product until pH=1, then filtering said first product; flushing said first product using water and drying said first product; taking N,N′-dicyclohexylcarbodiimide and N-hydroxysuccinimide to react with said first product for converting to a second product, wherein said second product includes a byproduct dicyclohexylurea; flushing and filtering said second product using ethyl acetate for eliminating said dicyclohexylurea; taking said second product and triglycine to perform an amide bonding reaction and producing a reaction product; using acetone to recrystallize said reaction product for forming a crystal product; filtering said crystal product; and using a flushing agent having an alkyl structure to flush the crystal product and producing a final product.

2. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 1, wherein said first product is S-benzoylsulfanylacetic acid.

3. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 1, wherein said first product and said N,N′-dicyclohexylcarbodiimide are carboxylated first to form an unstable complex.

4. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 3, wherein nucleophilic substitution of said complex by said N-hydroxysuccinimide is performed to produce said second product.

5. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 1, wherein said second product is an ester compound corresponding to said S-benzoylsulfanylacetic acid.

6. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 1, wherein said reaction product and said final product have different crystalline shapes.

7. The method for preparing S-Bz-MAG3 as a precursor of contrast media of claim 1, wherein said flushing agent utilized to flush the crystal product is dichloromethane.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows a flowchart of the method for preparing according to the present invention;

(2) FIG. 2 shows a path diagram for preparing S-Bz-MAG3 according to the present invention; and

(3) FIG. 3 shows a comparison table for preparing S-Bz-MAG3 according to the present invention.

DETAILED DESCRIPTION

(4) In order to make the structure and characteristics as well as the effectiveness of the present invention to be further understood and recognized, the detailed description of the present invention is provided as follows along with embodiments and accompanying figures.

(5) Given that the demands in domestic nuclear medicine imaging is increasing, the present invention provides a method for preparing S-Bz-MAG3 as a precursor of contrast media to solve the problems.

(6) In the following, the properties, the accompanying structures, and the method provided by the method for preparing S-Bz-MAG3 as a precursor of contrast media according to the present invention will be described.

(7) Please refer to FIG. 1 and FIG. 2, which show a flowchart of the method for preparing and a path diagram for preparing S-Bz-MAG3 according to the present invention. As shown in the figures, the method for preparing S-Bz-MAG3 as a precursor of contrast media according to the present invention comprises steps of:

(8) S1: Taking thioglycolic acid and benzoyl chloride for performing a thiol protection reaction and producing a first product;

(9) S3: Taking N,N′-dicyclohexylcarbodiimide and N-hydroxysuccinimide to react with the first product for converting to a second product;

(10) S5: Taking the second product and triglycine to perform an amide bonding reaction and producing a reaction product;

(11) S7: Using acetone to recrystallize the reaction product for forming a crystal product;

(12) S9: Filtering the crystal product; and

(13) S11: Using a flushing agent having an alkyl structure to flush the crystal product and producing a final product.

(14) As shown in the step S1, while adding the benzoyl chloride to the thioglycolic acid, the speed must be quite slow. The rate of adjusting the pH value should not be too fast. Otherwise, the productivity will be influenced.

(15) Thereby, as shown in the step S1, when the reaction time is longer, such as the time required for recovering to the room temperature and the time of adding the benzoyl chloride and stirring slowly (extending from 30 minutes to 2 hours), the productivity of a first product can be increased from 83% to 92%.

(16) In addition, as shown in the step S1, after the step of performing the thiol protection reaction, the method further comprises steps of filtering the first product and flushing the first product using water; and drying the first product for increasing the productivity of the first product.

(17) The first product produced in the step S1 is S-benzoylsulfanylacetic acid. As shown in the step S3, the first product and the N,N′-dicyclohexylcarbodiimide are carboxylated first to form an unstable highly active complex.

(18) Next, in the step S3, nucleophilic substitution of the highly active complex by the N-hydroxysuccinimide is performed to produce a second product.

(19) The second product produced in the step S3 is an ester compound corresponding to the S-benzoylsulfanylacetic acid.

(20) Besides, as shown in the step S3, the second product further includes a byproduct dicyclohexylurea.

(21) The dicyclohexylurea produced in the above step S3 is not solvable in organic solvents. Although the filtering method can be adopted for elimination, minor dicyclohexylurea still might be residual in the solution. Once elimination is not complete before the next experiment, the melting point of the S-Bz-MAG3 will be influence and hence influencing the productivity.

(22) Accordingly, as shown in the step S5, before the step of performing the amide bonding reaction, the method further comprises a step of flushing and filtering the second product using a solvent having a methyl structure for eliminating the dicyclohexylurea of the second product.

(23) In addition, as the above step S5, the solvent further includes ethyl acetate and acetone. Moreover, the flushing and filtering should be repeated for two more times for eliminating the dicyclohexylurea completely.

(24) As shown in the steps S5, S7, S9, S11, a reaction product produced in the step S5 and the final product, which is produced by recrystallizing by acetone in the step S7, filtering in the step S9, and flushing using a flushing agent having an alkyl structure in the step S11, have different crystalline shapes.

(25) As shown in the step S11, the flushing agent is dichloromethane.

(26) Compared with the total productivity of the prior art (24˜52%), the total productivity using the method for preparing S-Bz-MAG3 as a precursor of contrast media according to the present invention (64%) is higher with the purity greater than or equal to 98%.

(27) In the following, an experimental flow according to a preferred embodiment of the present invention will be described.

(28) The method for preparing the first product according to a preferred embodiment of the present invention is to solve thioglycolate (4.6 g, 0.10 mol) in 37.5 mL methylbenzene solution and sodium hydroxide (4.4 g, 0.22 mol) in 37.5 mL deionized water. The both are mixed in an ice bath and the temperature is maintained at around 10□. The reaction bottle is equipped with an isobaric tube and the benzoyl chloride (7.0 g, 0.10 mol) is added drop by drop. Stir for 30 minutes at 10□. Then continue to stir for 2 hours at the room temperature (28□). After the reaction is finished, the solution is placed in a separatory funnel. Take the lower layer (the water layer), and flush the organic layer using deionized water for four times. Next, adjust the pH value of the whole liquid-phase aqueous solution to 1 using concentrated hydrochloric acid. Filter to keep the white solid matter. Flush the solid matter using iced water and dry it to produce the white solid product (8.9 g, 92%).

(29) The data analysis for the first product according to the present invention is: IR (KBr): 1708 cm.sup.−1 (—COOH), 1665 (—S—C═O) cm.sup.−1. 1H NMR (CDCl3, 300 MHz): δ 7.99-7.95 (dd, 2H), 7.62-7.57 (t, 1H), 7.49-7.44 (t, 2H), 3.92 (s, 2H). 13C NMR (CDCl3, 75 MHz): 190.73, 175.33, 136.57, 134.67, 129.45, 128.16, 31.81. ESI-MS: m/z 197.01 (M+H)+.

(30) The method for preparing the second product according to a preferred embodiment of the present invention is to solve the first product (2 g, 0.0102 mmole) and NHS (1.17 g, 0.01017 mol) in 12.5 mL anhydrous tetrahydrofuran (THF) and lower the temperature to 0° C. Solve DCC (2.52 g) in 8.5 mL anhydrous THF and add the solution to the above solution using an isobaric tube. Afterwards, the for 2 hours at 0° C. Then recover to the room temperature and react overnight. Filter the reaction solution and flush twice using hot THF. Then dry the filtered solution. After recrystallizing using ethyl acetate, the white solid product (2.6 g, 86%) will be produced.

(31) The data analysis for the second product according to the present invention is: IR (KBr): 1820 cm.sup.−1, 1780 cm.sup.−1 and 1750 (ester) cm.sup.−1, 1680 (—S—C═O) cm.sup.−1, 1630 (—N—C═O) cm.sup.−1. 1H NMR (CDCl3, 300 MHz): δ 8.00-7.96 (dd, 2H), 7.64-7.47 (t, 1H), 7.47-7.44 (t, 2H), 4.17 (s, 2H), 2.83 (s, 4H). 13C NMR (CDCl3, 75 MHz): 189.28, 169.29, 165.42, 136.25, 134.81, 129.49, 128.24, 28.91, 26.22.

(32) The method for preparing the final product according to a preferred embodiment of the present invention is to mix the second product (1.35 g, 4.6 mmol) in 7 mL acetonitrile and heat it to around 60° C. for solving it. In addition, solve triglycine (870.82 mg, 4.6 mmol) in 1 N sodium hydroxide (4.5 mL). The solution is added to the previous solution and stir for 1 hour at 60° C. Then cool down to the room temperature and react for 5 hours. Filter out the insoluble matter and flush using water. Next, add concentrated hydrochloric acid (0.55 mL) to the filtered solution. The acidized solution is moved to a refrigerator (around 4° C.) for 4 hours. Filter the sediment, flush using cold water, and dry it. The coarse product is suspended in water and heated to 65° C. Besides, hot acetone is added to help solving. By cooling slowly, crystals are produced. After filtering the crystals and flushing using dichloromethane, the pure final product (1.38 g, 82%) will be produced.

(33) The data analysis for the final product according to the present invention is: IR (KBr): 3290 (—NH), 1708 (—COOH), 1665 (—S—C═O), 1649 (—N—C═O). 1H NMR (DMSO-d6, 300 MHz) 12.5 (s, COOH), 8.48-8.44 (t, 1H), 8.20-8.12 (q, 2H), 7.96-7.92 (dd, 2H), 7.71-7.67 (t, 1H), 7.56-7.54 (t, 2H), 3.88 (s, 2H), 3.74-3.77 (m, 6H). 13C NMR (DMSO-d6, 75 MHz): 190.30, 171.02, 169.04, 168.82, 167.17, 135.92, 134.05, 129.13, 126.86, 42.46, 42.71, 32.42. ESI-MS: m/z 368.12 (M+H)+, 390.11 (M+Na)+. DSC: melting point 200.97° C. HPLC: Purity 99.5% (Elution A: 1% Acetic acid, Elution B: Methanol, Elution A/Elution B=1/9 (v/v); Column: Chromolith Performance RP-18e (4.6 mm*100 mm); Detection: UV 254 nm; flow rate: 0.3 mL/min, RT=10.4 min).

(34) Please refer to FIG. 3, which shows a comparison table for preparing S-Bz-MAG3 according to the present invention. The examination specifications for raw material of the radiopharmaceutical MAG3 Betiatide (final product) must comply with the following four standards: 1. White power, slightly soluble in water, soluble in dimethyl sulfoxide (DMSO); 2. The range of melting point; 3. Purity lower than 98%; and 4. The NMR diagram compliance.

(35) According to documents, the melting point of S-Bz-MAG3 is 195˜197□. According to the website of the ABX, the range of melting point of the commercial S-Bz-MAG3 (Product code: 7100) is 192˜205□. The most possible impurity in the present synthesis method is the byproduct DCU produced while synthesizing the second product. DCU is not soluble in organic solvents. Although it be can eliminated by filtering, minor residues can still exist in the solution. It is inferred that the solution is not processed clean. The cleaner the sample is processed, the high the melting point will be.

(36) As shown in FIG. 3, the residual DCU indeed will influence the melting point. It is recommended to flush using ethyl acetate or acetone and filter twice before it is completely clean.

(37) Accordingly, the present invention conforms to the legal requirements owing to its novelty, nonobviousness, and utility. However, the foregoing description is only embodiments of the present invention, not used to limit the scope and range of the present invention. Those equivalent changes or modifications made according to the shape, structure, feature, or spirit described in the claims of the present invention are included in the appended claims of the present invention.