GB2090252A - N-substituted Iminodiacetic Acids - Google Patents

Abstract

New compounds having the formula <IMAGE> or a pharmaceutically acceptable, water soluble salt thereof, wherein R1 and R4 are each independently hydrogen, methyl or ethyl; one of R2 and R3 is alkyl of 1 to 4 carbons and the other is bromine or iodine; and n is 0, 1 or 2, when complexed with technetium-99m in the presence of a reducing agent provide compositions which are useful for the external imaging of the hepatobiliary system.

Description

SPECIFICATION N-Substituted Iminodiacetic Acids The present invention relates to a compound having the formula

or a pharmaceutically acceptable, water soluble salt thereof, wherein R, and R4 are each independently hydrogen, methyl or ethyl; one of R2 and R3 is alkyl of 1 to 4 carbons and the other is bromine or iodine; and n is 0, 1 or 2: and this invention also encompasses compositions comprising the compounds of formula I (and salts thereof) and a reducing agent, which are suitable for complexing with technetium99m. In formula I, and throughout the specification, the symbols are as defined above.

Complexes of technetium-99m and a compound of formula I are useful for the external imaging of the hepatobiliary system. The complexes have good specificity (i.e., when injected into a mammal a large percentage of the complex passes through the liver into the bile) and they exhibit rapid transport from liver to bile allowing for good biliary measurements.

With the exception of the brain, the liver is the organ most frequently examined by nuclear medicine procedures. Most of these studies involve the intravenous administration of labeled particles such as Tc-99m sulfur colloid which are effectively trapped by the Kupffer cells. The diagnostic information thus obtained is useful for studying liver morphology and Kupffer cell function. The optimum agent for these studies would have rapid, exclusive uptake into healthy Kupffer cells and would be biodegradeable and non-toxic.

Radionuclide studies are also used to measure hepatocyte function and bile duct patency (including gallbladder function). The optimum agent for these studies would have rapid, exclusive uptake by the hepatocytes, rapid intrahepatic transit, and prompt excretion into the biliary system. High specificity is required to obtain maximum diagnostic information while limiting patient radiation dose.

The time to maximum liver concentration (tax) and the time for the liver concentration to decrease to 50% of the concentration at tmax (t50) should both be short to reduce the time required for a study. This is important in patients that cannot be immobilized for long periods of time. Shorter study times increase the number of patients that can be handled in a given period of time maximizing the use of imaging equipment. A short t50 also means an increase in the ratio of radioactivity within the bile to that within the liver, thereby resolving the intrahepatic ducts from the liver and thus improving the quality of the image and of the resultant diagnosis.

Until recently, most of the nuclear medicine biliary function studies were performed with 1-131 rose bengal or 1-131 bromosulfophthalein. Although 1-1 31 rose bengal is usually the standard for comparing liver function agents, its photon energy is not optimum for gamma camera imaging, and the patient exposure to non-diagnostic beta radiation limits the dose which can safely be administered.

Image resolution and, therefore, diagnostic information is limited.

The development of Tc-99m penicillamine by Tubis et al (Radiopharmaceuticals, Subramanian et al, eds., The Society of Nuclear Medicine, Inc., New York, 1975, pgs 55-62) in 1974 was a significant step in overcoming the limitations of the iodine-131 label and in stimulating research interest in technetium-99m labeled hepatobiliary agents, Among the most useful technetium-99m labeled agents developed to date are the N-substituted iminodiacetic acids (hepatoiminodiacetic acids HIDA's). Loberg et al., in United States patent 4,017,596 disclose, inter alia, the use of a chelate of technetium-99m and a substituted iminodiacetic acid for external organ imaging. Eckelman et al., in United States patent 3,725,295 disclose the labeling of diethylenetriaminepentaacetic acid (DTPA) with technetium-99m.

The various HIDA derivatives which have been disclosed in the literature can be represented by the formula

The analogs discussed include the 2,6-dimethyl derivative (Loberg et al., U.S. Patent 4,017,596); 2,6 diethyl, 2,6-diisopropyl, 2-butoxy, 4-butoxy, 4-butyl, 4-isopropyl, 4-ethoxy and 4-iodo derivatives (Wistow et al., Radiology, 128: 793-794, 1 978); 2,3-dimethyl, 2,4-dimethyl, 2,5-dimethyl, 3,4- dimethyl and 3,5-dimethyl derivatives (Van Wyk et al., Eur.J. Nucl. Med., 4: 44548, (1979); and 2,4,6-trisubstituted derivatives wherein at least two of the substituents are alkyl of 1 to 4 carbons, the third substituent is hydrogen or alkyl of 1 to 4 carbons, and together the substituents contain at least three carbons (Belgian patent 855,107): and 2,6-dimethyl, 2,6-diethyl, 2,6-diisopropyl, 4-methyl, 4- ethyl, 4-isopropyl, 4-n-butyl, 4-n-pentyl, 4-t-butyl, 4-phenyl, 4-methoxy, 3,5-dimethyl, 2,4,6-trimethyl, 2,4, 5-trimethyl, 44luoro, 2,4-difluoro, 2,5-difluoro, and 2,3,4,5,6-pentafl uoro derivatives (Molten et al., 3rd Int. Symp. Radiopharm, Chem., St. Louis, Mo., June 1980).Fields et al, Journal ofLabelled Compounds andRadiopharmaceuticals, XV: 387-399 (1978) disclose N-(2phenethylcarbamoylmethyl)-iminodiacetic acid.

Van Wyk et al., Eur. J. Nucl. Med, 4: 44548, 1979, in their work with dimethyl HIDA derivatives have shown that steric effects of substituents are important for biliary uptake. Chiotellis et al., tnt. J. Null. Med. Blot., 7: 7:1-7, 1980, working with 4-butyl HIDA compounds, have shown that molecular size of substituents is important for biliary uptake.

Compounds of formula I of the present invention, and salts thereof, can be labeled with technetium-99m and subsequently administered intravenously into a patient for the purpose of imaging the hepatobiliary system. The radiolabeling of compounds of formula i, and salts thereof, can be accomplished using procedures well known in the art. In a preferred procedure, technetium-99m in the form of an aqueous sodium pertechnetate solution (Na99mTcO4) is combined with a reducing agent and a compound of formula I, or salt thereof. While the order of mixing of the three abovedescribed components is not critical it is most preferred that the reducing agent be first combined with a compound of formula I of this invention.This composition (a non-radioactive composition) can then be supplied to radiochemists, technicians, radiopharmacists, doctors and the like for labeling with technetium-99m just prior to use.

Stannous ion is the preferred reducing agent. Exemplary stannous reducing agents are stannous chloride and stannous fluoride. Technetium-99m in the form of an aqueous solution of sodium pertechnetate is readily obtainable from commercially available molybdenum-99/technetium-99m generators which are conventionally eluted with saline.

The compounds of formula I of this invention can be prepared using as starting materials nitrilotriacetic acid, acetic anhydride, and an amine derivative having the formula

Nitrilotriacetic acid and acetic anhydride are first reacted to give nitrilotriacetic anhydride which is then reacted with an amine of formula Il to give the corresponding compound of formula I. The reactions proceed most readily if the reactants are present in stoichiometric amounts.

The compounds of formula I can be converted to pharmaceutically acceptable, water-soluble salts using art-recognized procedures. Preferred salts are alkali metal salts and alkaline earth metal salts.

The compounds of formula I (and salts thereof) can be prepared for complexing with technetium 99m using art-recognized procedures. For example, a "wet kit" can be prepared by first dissolving a compound of formula I (or salt thereof) in base (e.g., sodium hydroxide) to give a solution of about pH 6 to 7. To this solution is added an acidic solution of reducing agent (e.g., stannous fluoride) in hydrochloric acid. Water can be added to give the desired volume. To this solution technetium-99m, preferably an aqueous solution of sodium pertechnetate, can be added. Lyophilized kits can be prepared using the above-described procedure, except that prior to the addition of technetium-99m the solution is lyophilized. The lyophilized material may be stored in an inert atmosphere.

Preferred compounds of this invention are those compounds of formula I wherein n is 0.

Particularly preferred are those compounds having the formula

or a pharmaceutically acceptable, water soluble salt thereof, wherein one of R2, and R3, is methyl or ethyl and the other is bromine or iodine.

The following examples are specific embodiments of this invention.

Example 1 2,2'-[(2-[(3-Bromo-2,4,6-trimethylphenyl)amino]-2-oxethyl] imino]bisacetic Acid A) 3-Bromo-2,4,6-trimethylaniline Concentrated hydrochloric acid (80 ml) is cooled in an ice-water bath to 50C. 2,4,6- Trimethylaniline (13.5 g) is added over a period of 20 minutes with vigorous stirring while keeping the temperature below 1 50C. The thick slurry is cooled to 30C and 16.8 g of bromine in 80 ml of concentrated hydrochloric acid is added over a period of 25 minutes. The slurry is heated in a water bath for one hour and then cooled in an ice bath for one hour. The reaction mixture is then filtered and the salt is washed with three 50 ml portions of cold distilled water.After drying, the crude product is dissolved in 600 ml of distilled water, treated with 3.0 g of Darco and filtered on a Hyflo-bed to give a solution. Neutralization with concentrated ammonium hydroxide gives a milky solution from which the product solidifies upon cooling to 1 00C. After refrigeration for about 1 6 hours, the tan product is filtered, washed with cold distilled water and dried under vacuum for about 1 6 hours to give 12.0 g of the title compound, melting point 34.0--35.00C.

B) 2,2'-[[2-[(3-Bromo-2,4,6-trimethylphenyl)amino]-2-oXoethyl]imino]bisacetic Acid A suspension of 9.56 g of nitrilotriacetic acid in pyridine (dried over molecular sieves) is prepared with the exclusion of moisture (CaSO4 drying tube) and heated to 500C. Acetic anhydride (5.11 g) is added dropwise. The reaction mixture clears and is heated to 1000C. After maintaining the temperature for 40 minutes, the reaction mixture is cooled to 550C and a solution of 10.7 g 3-bromo2,4,6-trimethylaniline in 25 ml of dry pyridine is added slowly. The reaction is heated to 1000C and after 1.5 hours at this temperature, the solution is cooled in an icebath.The reaction mixture is rotary evaporated to a semisolid which is dissolved in 125 ml of 10% sodium hydroxide w/v. The basic layer is than extracted with two 100 ml portions of methylene chloride. Distilled water (100 ml) is added to the basic layer which is then brought to pH 3 with concentrated hydrochloric acid to give a precipitate.

After refrigeration for about 1 6 hours, the crude product is filtered, washed with cold distilled water and dried under vacuum at 400 C. The crude product is dissolved in 100 ml of 60% aqueous ethanol, treated with 3.0 g of Darco and filtered hot through a Hyflo-bed to give a solution. Crystals precipitate and are filtered, washed with three 25 ml portions of 50% aqueous ethanol and dried under vacuum at 400 C. The reaction yields 9.1 g of the title compound, melting point 1 98--2000C, dec.

Example 2 2,2'-[[2-[(3-[(3-Bromo-2,6-diethyl-4-methylphenyl)-amino]-2-oxoethyl]imino]bisacetic Acid A) 3-Bromo-2,6-diethyl-4-methylaniline Concentrated HC1 (10 ml) is cooled to 50C in an ice-water bath and 1.63 g of 2,6-diethyl-4methylaniline is added dropwise to give a slurry. Bromine (1.59 g) with 10 ml of concentrated HCI is added dropwise over 30 minutes. The reaction is allowed to stir for 3.75 hours and 25 ml of distilled water is added. After cooling for 1.0 hour, the reaction mixture is filtered and washedstwice with 25 ml of cold distilled water.After drying under vacuum for about 1 6 hours, the crude solid (2.3 g) is dissolved in 100 ml of 10% NaOH and extracted with a 1 50 ml portion and with a 100 ml portion of methylene chloride. After drying over sodium sulfate, the methylene chloride solution is rotary evaporated to 1.9 g of crude product.

B) 2,2'-[[2-[(3-Bromo-2,6-diethyl-4-methylphenyl)-aminoi-2-oxethyl]iminojbisacetic Acid A slurry of 1.34 g of nitrilotriacetic acid in 1 5 ml of dry pyridine (dried over molecular sieves) is prepared and heated to 460C. Acetic anhydride (0.72 g) is added (1 ml pyridine rinse) and the solution is heated to 1000C. After heating for 0.5 hour, the solution is allowed to cool to 460C and a solution of 1.7 g of crude 3-bromo-2,6-diethyl-4-methylaniline in 6 ml of pyridine is slowly added. The solution is heated at 1000C for 2 hours, cooled, and rotary evaporated to a pasty product. The product is dissolved in 25 ml of 10% sodium hydroxide and the resulting solution is extracted twice with 25 ml portions of methylene chloride.The aqueous solution is diluted with 50 ml of distilled water, neutralized with concentrated HC1 to pH 3.0, and refrigerated for about 16 hours. Filtration gives a solid which upon drying for 3 hours at 600C under vacuum gives 1.4 g of crude product.

Recrystallization from 25 ml of 50% ethanol gives 1.04 g of needles, melting point 194.5--195.50C.

Example 3 2,2'-[[2-[(3-lodo-4-methylphenyl)amino]-2-oxoethyl]-imino]bisacetic Acid A slurry of 4.78 g of nitrilotriacetic acid in 40 ml of dry pyridine (dried over molecular sieves) is heated to 600 C. Acetic anhydride (2.55 g) is added slowly and the solution is heated to 1000C. After heating for 0.5 hour, the solution is cooled to 400C and a solution of 5.8 g of 3-iodo-4-methylaniline in 20 ml of dry pyridine is added over 25 minutes. The solution is heated at 1000C for 1.0 hour. The reaction is cooled and rotary evaporated to a residue which is dissolved in 65 ml of 10% sodium hydroxide. This solution is extracted twice with 50 ml portions of methylene chloride diluted with 100 ml of distilled water, and neutralized with concentrated HC1 to pH 3.2.The crude product is refrigerated for about 1 6 hours, filtered, washed twice with 50 ml portions of distilled water, and dried under vacuum at 400 C. The crude product (8.0 g) is recrystallized after Darco treatment to yield 5.7 g of product, melting point 213.5--21 5.000 (dec).

Example 4 2,2'-[[2-[(4-Bromo-3-methylphenyl)a minoj-2-oxoethyljimino]bisacetic Acid A slurry of 9.56 g of nitrilotriacetic acid in 80 ml of dry pyridine (dried over molecular sieves) is heated to 550C. Acetic anhydride (7.66 g) is added and the solution is heated to 1000C. After heating for 0.5 hour, the solution is cooled to 550C and 9.30 g of 4-bromo-3-methylaniline is added with a 5 ml pyridine rinse. The solution is heated at 1000C for 1.0 hour. The reaction is cooled and rotary evaporated to a pasty solid which is dissolved in 120 ml of aqueous ammonium hydroxide (30 ml concentrated ammonium hydroxide/90 ml distilled water).The clear brown solution is extracted with two 100 ml portions of methylene chloride and neutralized to pH 3 with 35 ml of concentrated HC1.

The white solid is filtered, washed with three 25 ml portions of cold distilled water, and dried under vacuum for 2.75 hours at 600C. The crude product (12.9 g) is recrystallized from 360 ml of 50% ethanol to give 9.85 g.of product, melting point 206.5--209.00C.

Example 5 2,21-[[2-[(3-Brnmo-4-methylphenyl)aminoj-2-oxoethyl]-imino]bisacetic Acid A slurry of 4.78 g of nitrilotriacetic acid in 40 ml of dry pyridine (dried over molecular sieves) is prepared and heated to 500 C. Acetic anhydride (2.55 g) is added slowly and the solution is heated to 1000C. After heating for 0.5 hour, the solution is cooled to 420C and 4.81 g of 3-bromo-4methylaniline in 5 ml of pyridine is slowly added. The solution is heated to 1000C. After heating for 2.0 hours, the reaction is cooled and rotary evaporated. This material is dissolved in 75 ml of 10% sodium hydroxide, and extracted twice with 50 ml portions of methylene chloride.The aqueous portion is diluted with 100 ml of distilled water, neutralized to pH 3.2 with concentrated HCI, and refrigerated for about 1 6 hours overnight. The reaction is filtered and washed with cold distilled water After drying for 3 hours under vacuum at 600C, 7.14 g of crude product is obtained, melting point 206.0- 208.00 C. Recrystallization from 1 50 ml of 75% ethanol gives 6.4 g of solid, melting point 209.0- 210.000.

Example 6 Formulations for Complexing with Technetium-99m The table below presents exemplary formulations of compounds of formula I with stannous fluoride reducing agent. The formulations are prepared by dissolving the ligand in 0.46 M sodium hydroxide to give a solution of final pH of about 6 to 7.5. To this is added 0.01 ml of a 70 mg/ml solution of stannous fluoride in 6M hydrochloric acid and the volume is brought to 5 ml with water for injection. The formulations in the following table have a preferred molar ratio of ligand: tin of 150:1.

Table Concentration (mg/mt) stannous Ligand ligand fluoride pH 2,2'-[[2-[(3-Bromo-2,4,6-trimethylphenyl)- 48.6 0.14 6.76 amino]-2-oxoethyllimino]bisacetic acid 2,2'-[[2-[(3-[(3-Bromo-2,6-diethyl-4- 51.9 0.14 5.99 methylphenyl)amino]-2-oxoethyl]imino] bisacetic acid l 2,2'-[[2-[(3-lodo-4-methylphenyl)amino]- 50.4 0.14 7.55 2-oxoethyl]imino]bisacetic acid 2,2'-[[2-[(4-Bromo-3-methylphenyl)aminoj- 44.6 0.14 5.96 2-oxoethyl]imino]bisacetic acid 2,2'-[[2-[(3-Bromo-4-methylphenyl)amino]- 44.9 0.14 7.39 2-oxoethyl]imino]bisacetic acid

Claims (9)

Claims

1. A compound having the formula

or a pharmaceutically acceptable, water soluble salt thereof, wherein: R, and R4 are each independently hydrogen, methyl or ethyl; one of R2 and R3 is alkyl of 1 to 4 carbons and the other is bromine or iodine; and n is O, 1 or 2.

2. A compound in accordance with claim 1 having the formula:

or a pharmaceutically acceptable, water-soluble salt thereof.

3. A compound in accordance with claim 1 or 2 wherein R1 and R4 are both methyl.

4. A compound in accordance with claim 1,2 or 3, or a pharmaceutically acceptable, watersoluble salt thereof, wherein one of R2 and R3 is methyl or ethyl.

5. The compound in accordance with claim 1, 2,2'-[2-[(3-brnmo-2,4,6-tflmethylphenyl)amino]- 2-oxoethyl]imino]bisacetic acid.

6. The compound in accordance with claim 1, 2,2'-[[2-[(3-bromo-2,6-diethyl-4- methylphenyl)amino]-2-oxoethyl]imino]bisacetic acid.

7. The compound in accordance with claim 1, 2,2'-[[2-((3-iodo-4-methylphenyl)aminoj-2- oxoethyl]-imino]bisacetic acid.

8. The compound in accordance with claim 1, 2,2'-[[2-[(4-bromo-3-methylphenyl)amino]-2- oxoethyl]imino]bisacetic acid.

9. The compound in accordance with claim 1, 2,2'-[[2-3-brnmo-4-methylphenyl)aminoj-2- oxoethyl]i mino]bisacetic acid.

1 0. A composition comprising a stannous reducing agent and a compound in accordance with any one of claims 1 to 9.