BACKGROUND OF THE INVENTION Technical Field The subject matter of the present invention relates to bifunctional cyclohexyl DTPA ligands and methods of using these compounds. Specifically, such ligands are useful for radiolabeling proteins with radio¬ active metals, and can consequently be utilized with respect to radioimmunoimaging and/or radioimmunotherapy. Background Information

This invention relates to metal chelates and the use of metal-chelate protein conjugates.

Interest in the art of metal chelates and in methods for forming metal chelate-protein conjugates for diagnostic and therapeutic purposes continues. Represen¬ tative type chelates and conjugates and methods for forming conjugates are disclosed, inter alia, in U.S. Pat. Nos. 4,454,106, 4,472,509, 4,339,426, in EPA 0 279 307 and in German Patent 1,155,122. Other proteins including antibodies, monoclonal antibodies and fragments thereof, monoclonal antibodies and fragments thereof which have been structurally altered by recombinant DNA techniques (i.e., chimeric antibodies), polyclonal antibodies, antigens, blood proteins, or proteins bound to blood lymphocytes or other cells can also be employed in the formation of conjugates.

A method for synthesis of bifunctional metal chelates for conjugation to proteins involves reduction of amino acid amides to ethylenediamines to form monosubsti- tuted derivatives which are converted to bifunctional ethylenedia inetetraacetic acid (EDTA) chelates by alkyla- tion with haloacetic acid. (Yeh et al., Anal. Biochem. 100: 152 (1979)). Similarly, a monosubstituted diethylenetria ine is synthesized by reaction of ethylene- diamine with an amino acid ester and reduction of the resulting amide carbonyl. (Brechbiel et al. Inor . Chem. 25: 2772-81 (1986)). Alkylation of the diethylenetriamine with haloacetic acid produces a monosubstituted bifunc-

with haloacetic acid produces a monosubstituted bifunc¬ tional diethylenetriaminepentaacetic acid (DTPA) chelate.

Another method of synthesis of a bifunctional DTPA involves reaction of a DTPA or EDTA carboxylate with a chloroformate ester to form a reactive anhydride. (Krejcarek et al., Biochem. Biophys Res. Commun. 77:581 (1977)). The dianhydride of DTPA used as a bifunctional chelate is prepared by dehydration of the parent DTPA. (Hnatowich et al., Int. J. APPI. Rad. Isot. 33:327 (1982)). The practice of using an EDTA chelate monosub¬ stituted at the carbon-1 position to better retard the release of metal from chelate in vitro. than the unsubsti- tuted EDTA chelate, has also been reported. (Meares et al., Anal. Biochem. 142:68 (1984)). The prior art has formed metal-protein chelate conjugates by mixing monosubstituted bifunctional EDTA or DTPA chelates, or DTPA anhydrides with proteins followed by reaction with the metal to be chelated. (Krejcarek et al., Biochem. Biophys. Res. Commun. 77:581, (1987); Brechbiel et al., Inor . Chem. 25:5783 (1986)). Imaging of tumor target sites in vivo with metal chelate conju¬ gated monoclonal antibodies prepared according to these methods has been reported. (Khaw et al., Science 209:295, (1980); Sheinberg et al., Science 215:151, (1982)). Diagnosis of human cancer in vivo using metal chelate conjugated monoclonal antibody has also been reported. (Rainsbury et al., Lancet 2:694 (1983)). The use of chimeric antibodies and advantages thereof have been discussed by Morrison, S.L., Hospital Practice (Office Edition) 24:64-65, 72-74, 77-80 (1989). The potential efficacy of using a linking group within a chelate conju¬ gated protein has also been discussed (Paik et al., J. Nucl. Med. 30:1693-1701 (1989)).

However, attempts to employ the tumor localizing properties of metal chelate conjugated monoclonal anti¬ bodies for therapeutic purposes have not found common usage. This is, in part, because metals may be (and often are) released from the metal chelate conjugate in vivo.

Particularly, radioactive metal salts may produce unde¬ sirable concentrations of toxic radionucleotides in bone marrow or kidney or the like, even if the conjugates are rigorously purged of adventitiously bonded metal. A process for purifying metal chelate protein conjugates of adventitiously bonded metals is disclosed in U.S. Pat. No. 4,472,509. The importance of using very strong metal chelates to firmly link radiometals to monoclonal anti¬ bodies and of rigorous purification of the conjugates to effect maximal tumor localization and minimize delivery to non-target tissues is discussed in Brechbiel et al., Inor . Chem. 25:2772-81 (1986)). Undesirable localization of potentially therapeutic radionuclides released in mice in vivo from metal chelate conjugated polyclonal anti- bodies have precluded some therapy investigations in humans. (Vaughn et al., EIR-Bericht. Vol. 78, (1986)). Increased in vivo bone uptake of radiometal injected for therapy as a metal chelate conjugated monoclonal antibody has also been reported. (Hnatowich et al., J. Nucl. Med. 26:503 (1985)). The amount of potentially therapeutic doses in humans of radiometal chelated polyclonal antibody has been limited by bone marrow toxicity (Order et al., Int. J. Rad. Oncol. 12:277 (1986)). Kidney uptake of radiometal has recently been reported as preventing human use. (Macklis et al, Science. 240:1024-26 (1988)).

Disubstituted bifunctional DTPA derivatives have proven useful for the labeling of proteins with radioac¬ tive metals (Kozak, et al., Cancer Research 49:2639-44 (1989)). The introduction of a second substituent on the carbon backbone of DTPA was seen to retard the loss of metal from the DTPA ligand when linked to an antibody and injected into the circulation of animals.

The usefulness of radionuclide materials in cancer therapy is disclosed in the article, Kozak et al., "Radio- nuclide-conjugated monoclonal antibodies: A synthesis of Immunology, in Organic Chemistry and Nuclear Science" Trends in Biotechnology. 4(10):259-64 (1985). This article discusses the use of antibody conjugates to

deliver either alpha or beta radiation. The value of alpha radiation for bismuth-212 in radionuclide therapy is further discussed in the two articles, Kozak et al., "Bismuth-212-labeled anti-Tac monoclonal antibody: Alpha- particle-emitting Radionuclides as Modalities for Radio- mmunotherapy," Proc. Natl. Acd. Sci. U.S.A. 83:474-478 (1986) and Gansow et al., "Generator-produced Bi-212 Chelated to Chemically Modified Monoclonal Antibody for Use in Radiotherapy," Am. Chem. So. Symposium Series 15:215-227 (1984). Ligands, for the secure linkage of bismuth to proteins, have not been available. (Macklis et al., Science 240:1024-2 (1988)).

Examples of other uses for chelated metal ions are disclosed in the following articles. Magerstadt et al. , "Gd(DOTA) : An alternative to Gd(DPTA) as a T _1/2 Relax¬ ation Agent for NMR Imaging or Spectroscopy," Magnetic Resonance in Medicine 3:808-812 (1986), discloses the usefulness of gadolinium as a relaxation agent for NMR imaging. The article, Spirlet et al., "Structural Charac- terization of a Terbium (III) Complex with 1,4,8,11- Tetraazacyclotetradecane-1,4,8,11 tetraacetic acid. Lanthanide ^' Ions and Conformation of the 14-Membered Ring," Inorgan. Chem. 23:4278-4783 (1984), disclosed the useful¬ ness of lanthanide chelates. All patents and publications referred to herein are hereby incorporated by reference.

It is evident from the above that there continues to be a need for more effective metal chelate protein conjugates that firmly link metals to proteins to minimize metal release and permit highly selective delivery of metals to targeted sites in vivo.

SUMMARY OF THE INVENTION It is, therefore, an object of the present inven¬ tion to provide novel polysubstituted cyclohexyl diethylenetriamines.

It is another object of the present invention to provide novel polysubstituted bifunctional cyclohexyl diethylenetriaminepentaacetic acid ligands or chelates.

It is yet another object of this invention to provide novel ligand and chelate-hapten conjugates.

It is still a further object of this invention to provide novel metal chelate protein conjugates. It should be noted that the present invention overcomes an inherent synthetic barrier which limits the prior art to less than three ligand substituents without stereo-control.

The present invention includes a ligand co pris- ing:

(I)

wherein n is an integer from 1 to 5;

X equals -N0 ₂ , -NH ₂ , -NCS, or -NHCOCH ₂ -Z;

T denotes the trans isomer of the cyclohexyldiamine substructure; and

Z is chloride, bromide or iodide.

The invention also includes a metal chelate of the ligand wherein n is an integer from 1 to 5, X equals -NO,,

-NH-, -NCS, or -NHC0CH ₂ -Z, the metal is chosen from the elements consisting of Cu, Pb, In, Yt, Bi, the lan- thanides, Au, Ag, and Ga, and Z is chloride, bromide or iodide.

In addition, the invention includes a ligand- hapten conjugate comprising:

(ID wherein n is an integer from 1 to 5; X ¹ is NH-Q, NHCS-Q or -NHCOCH ₂ where Q is a hapten chosen from the group consisting of steroids, enzymes, proteins, monoclonal antibodies, chimeric antibodies,, or fragments thereof; and T denotes the trans isomer of the cyclohexyldiamine substructure.

Another embodiment of the invention includes the ligand-hapten conjugate wherein n is an integer from 1 to 5, X' is -NH-L-Q, -NHCS-L-Q, or -NHCOCH ₂ -L-Q, where Q is a hapten selected from the group consisting of steroids, enzymes, proteins, monoclonal antibodies, chimeric anti¬ bodies, or fragments thereof, and L is a covalent linking group.

A further embodiment includes the situation where L of the ligand-hapten conjugate is selected from the group consisting of an organic radical, or a substituted aliphatic hydrocarbon chain. The chain may be interrupted by one or more hetero atoms selected from -O- or -S-, or one or more -NR'- groups, where R' is a hydrogen atom or a C-l alkyl group, -CONR'- groups, -NR'CO- groups, cyclo- aliphatic, aromatic or heteroaromatic groups, or a mixture thereof.

A further embodiment includes the metal chelates of the ligand-hapten conjugate wherein n is an integer from 1 to 5, X' is equal to -NH-Q, -NHCS-Q or -NHCOCH ₂ .-Q,

where Q is a hapten selected from the group consisting of steroids, enzymes, proteins, monoclonal antibodies, chimeric antibodies, or fragments thereof, and the metal is selected from the group consisting of Cu, Pb, In, Yt, Bi, the lanthanides, Au, Ag, and Ga.

An additional embodiment includes the metal chelates of the ligand-hapten conjugate wherein n is an integer from 1 to 5, X' is equal to -NH-L-Q, -NHCS-L-Q or -NHCOCH ₂ -L-Q, where Q is a hapten selected from the group consisting of steroids, enzymes, proteins, monoclonal antibodies, chimeric antibodies, or fragments thereof, and the metal is selected from the group consisting of Cu, Pb, In, Yt, Bi, the lanthanides, Au, Ag, and Ga, and L is a covalent linking group. Another embodiment includes the situation where L of the metal chelates of the conjugate is selected from the group consisting of an organic radical or a substi¬ tuted aliphatic hydrocarbon chain. The chain may be interrupted by one or more hetero atoms selected from -0- or -S- or by one or more -NR'- groups, where R' is a hydrogen atom or a C,_ alkyl group, -CONR'- groups, -NCR'O- groups, cycloaliphatic groups, aromatic or hetero- aromatic groups, or a mixture thereof.

The present invention also includes the method of using the metal chelates of the ligand-hapten conjugate wherein said conjugate is administered to a patient as a therapeutic agent or diagnostic agent.

Furthermore, the present invention includes the method of using the metal chelates of the ligand-hapten conjugate possessing a linking group wherein the chelate as a therapeutic or diagnostic agent.

BRIEF DESCRIPTION OF THE DRAWINGS •FIGURE 1 represents a scheme for the preparation of a substituted cyclohexyl diethylenetriaminepentaacetic acid ligand (DTPA).

DETAILED DESCRIPTION OF INVENTION Unless specifically defined otherwise, all tech¬ nical or scientific terms used herein have the same

meaning as commonly understood by one or ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described.

The subject matter of the present invention relates to bifunctional cyclohexyl DTPA chelating agents or ligands and methods for using these compounds. Specif- ically, the ligands can be used in radioim unoimaging and/or radioim unotherapy, as the compounds may be uti¬ lized for labeling proteins with radioactive metals.

Monoclonal antibodies are immunoglobulins of well- defined chemical structure, in contrast to polyclonal antibodies which are heterogeneous mixtures of immuno¬ globulins. A characteristic feature of monoclonal anti¬ bodies is reproducibility of function and specificity, and such antibodies can be and have been developed for a wide variety of target antigens, including tumor cells.' More recently, chimeric monoclonal antibodies and fragments have been prepared by recombinant techniques (Morrison, S.L., Hospital Practice (Office EditionT 24: 64-65, 72-74, 77-80 (1989)).

Methods for obtaining monoclonal antibodies or fragments have been extensively discussed and are well- known in the art. A useful text is Monoclonal Antibodies (R. H. Kennett, T. J. McKearn & K. B. Bechtol eds. 1980). See also Koprowski et al.(U.S. Pat. No. 4,196,265). The selection of a monoclonal antibody for the practice of this invention will depend upon the end use for which the metal chelate conjugated monoclonal antibody will be employed. Such selection is within the skill of the art.

A wide variety of organic chelating agents or ligands can be conjugated to monoclonal antibodies. Organic ligands to be conjugated to monoclonal antibodies may be chosen from among either the natural or synthetic amines, porphyrins, aminocarboxylic acids, imi ocarboxylic acids, ethers, thiolε, phenols, glycols and alcohols or

the polyamines, polyaminocarboxylic acids, polyiminocar- boxylic acids, aminopolycarboxylic acids, i inopolycar- boxylic acids, nitrilocarboxylic acids, .dinitrilopolycar- boxlic acid, polynitrilopolycarboxylic acids, ethylenedia- minetetracetates, diethylenetriaminepenta or tetraace- tates, polyethers, polythiols, cryptands, polyether- phenolates, polyetherthiols, ethers of thioglycols or alcohols, polyaminephenols, all either acyclic, macro- cyclic, cyclic, macrobicyclic or polycyclic, or other similar ligands which produce highly stable metal chelates or cryptates.

The ligand of this invention possesses a nonmetal bonded organic functional group suitable for bonding to the monoclonal antibody. Functional groups may be chosen from among the carboxylic acid groups, diazotiazable amine groups, N-hydroxy-succinimidyl, esters, anhydrides, mixed anhydrides, maleimides, hydrazines, benzimidates, nitrenes, isothiocyanates, azides, sulfonamides, bro o- acetamides, iodocetamides, carbodiimides, sulfonyl- chlorides, hydroxides, thioglyols, or any reactive func¬ tional group known in the art as a biomolecular conju¬ gating or coupling agent.

The present invention is a derivative of diethyl- enetriaminepentaacetic acid (DTPA) . It has been found that DTPA ligands tightly bind metal ions and that the DTPA derivative of this invention forms a chelate conju¬ gated monoclonal antibody that is highly stable, both with respect to the metal chelate binding and with respect to chelate-antibody conjugate. These properties are of great importance, particularly for in vivo applications. For example, if the chelate releases the metal ion after introduction into the blood, these ions tend to be bound by transferrin, or the like, and be distributed generally in the circulatory system of the body. Moreover, the ions will ultimately tend to collect and remain in organs such as the liver and spleen, bone or kidney. These effects can have serious consequences depending on the toxicity of the metal and its radioactivity. Furthermore, if the

- 10 - chelate does not form a highly stable conjugate with the antibody, there is a significant reduction in the amount of metal delivered to the target site and a corresponding decrease in efficacy. If the conjugate is used for diagnostic purposes, release of the metal can undesirably increase background radiation.

The metals which may be employed in the present invention may include radioactive or nonradioactive elements with a valance of two or higher. Monovalent metals generally do not form sufficiently stable chelates for the purposes of this invention. Representative radioactive elements may include d-block transition metals, the group IIIA, IVA, VA metals, the lanthanides or the actinides. Nonradioactive metals may be selected, for example, for their useful physical properties such as paramagnetism, fluorescence, or phosphorescence. Repre¬ sentative nonradioactive metals include most lanthanides and some first row d-block elements. While this invention is discussed in terms of metals or metal chelates, it will be understood that metal ions are, in fact, chelated in the conjugate.

If ^" the metal chelate conjugated monoclonal anti¬ body is to be used for imaging in vivo, a gamma or posi¬ tron emitting radiometal, such as indium-Ill (gamma)- or gallium-68 (positron) , can be used depending upon the chosen method of detection. For purposes of therapy, the radiometals may be alpha (e.g. bismuth-212), beta (e.g. Pb-212, Y-90 or Cu-67 scandium -47) or Auger electron emitter. An alpha emitter, such as bismuth-212 is desir- ably employed for therapy. Paramagnetism, fluorescence and phosphorescence can be used, for example, for in vitro tests. The choice of any particular metal and valence state is within the skill of the art.

Metal chela ion is carried out in a solution and, desirably avoids the use of strong acids or bases. Metal chelation for any chelate-antibody conjugate is carried out at a pH which does not significantly reduce the biological activity or specificity of the antibody.

Generally, the acceptable range is from about pH 3.2 to about pH 9, however, particular antibodies may have to be restricted to a narrower range. At a pH above 3.5, adventitious binding of metal ions to antibodies is substantially impaired for many metals. A preferred range, therefore, is often from about pH 3.2 to about pH 3.5. Factors peculiar to solutions of the metal employed, however, may permit a pH about 3.5. The selection of the appropriate pH within the range is within the skill of the art.

Linkage of Bismuth ions to antibodies by use of metal chelates is a particularly difficult process. Only the iodide complexes label ligand linked antibodies effectively (Kozak et al., Proc. Nat. Acad. Sci. 83:474- 78 (1986)). Moreover, no chelating agents are currently available which bind bismuth securely in vivo (Macklis et al., Science. 240:1024-26 (1988)).

The functionalized DTPA ligand of the present invention is substituted at three carbon positions as is drawn in Formula I (shown below) in which X represents the nitro, amino, isothiocyanate or haloacetimide functional groups, n = 1 to 5., and the symbol T in the cyclohexane ring denotes the trans isomer of the diaminecyclohexyl substructure. The structure of Formula I is as follows:

The invention also includes the metal chelates of the ligand of Formula I. Preferably, the metals are chosen from the elements including copper, lead, indium,

yttrium, bismuth, the lanthanides, gold, silver, and gallium.

Particularly preferred embodiments of the inven¬ tion involve metal chelates of the ligand of Formula I with the radioactive isotopes In-Ill, Y-90, Bi-212, Pb- 202, Pb-212, Ga-66, Ga-67, Ga-68, and Cu-67.

The presence of three substituents on the carbon backbone of DTPA induces a maximal control of the stereo- chemical predisposition of the ligand towards effective metal complexation. In particular, it is well known to introduce the trans structure of the cyclohexyldiamine substructure of Formula I to increase metal complex thermodynamic stability as opposed to the incorporation of similar cis cyclohexyldiamine isomer as is the practice for the well characterized cis arid trans cyclohexyl-EDTA complexes. See data in A. E. Martell, Critical stability Constants, Vol. 1, Plenum Press, New York, (1974) . Additionally, the stereochemical constraint of the cyclo- hexane ring serves to direct and focus the lone pairs of the two amines to impart maximal overlap with available empty metal orbitals, as well as to maximize ligand-dipole to metal electrostatic bonding. This results in a DTPA ligand with optimized pre-control and pre-organization for metal ion binding thus reducing the entropy of metal complex formation as recorded in the reference above.

Other functionalized DTPA ligands which feature trisubstitution on the carbon backbone have been envi¬ sioned, but they lack the critical stereochemistry of the trans cyclohexyldiamine substructure of Formula I. See U. ^" S. Patent No. 4,831,175.

A principal advantage of the ligand of Formula I is that it forms complexes with bismuth ions that are stable in vivo. Such complexes of other substituted DTPA ligands are not stable in vivo, thus precluding their use in cancer therapy when linked to antibodies.

An additional feature of the ligands of this invention is that they form stable complexes in vivo with a wide variety of other radio etals which are used in

cancer detection and therapy. Such metal ions include- trivalent indium, yttrium, or scandium and divalent lead and copper. Indium-Ill is often used for tumor imaging. Thus, a patient could be imaged with the In-lll antibody conjugate of the ligand of this invention and thereafter treated with the bismuth-212 complex of the same antibody chelate conjugate, thus facilitating calculation of the dose of radioactivity transported to the patients tumor and so increasing likelihood of the effective application of the therapy. With dosimetry information, multiple dosing therapies can be designed.

Another embodiment of the invention is a ligand- hapten conjugate as is drawn in Formula II (shown below) in which the T in the cyclohexane ring denotes the trans isomer of the cyclohexyldiamine substructure, n is 1 to 5, and X' is -NH-Q, -NHC0CH--Q or NHCS-Q, where Q is a hapten chosen from the group consisting of steroids, enzymes, or proteins. Of particular interest within the subset of proteins are monoclonal antibodies, chimeric monoclonal antibodies, and the fragments thereof. The structure of Formula II is as follows:

A further embodiment of the invention is a ligand-hapten conjugate as is drawn in Formula II (shown above) in which the T in the cyclohexane ring denotes the trans isomer of the diamino cyclohexane substructure, n is 1 to 5, X' is -NH-L-Q, or -NHCS-L-Q, where Q is a hapten chosen from the group consisting of steroids, enzymes, or proteins, and L is a covalent linking group. Of particu¬ lar interest within the subset of proteins are monoclonal antibodies, chimeric monoclonal antibodies, and the fragments thereof. Such conjugates may be utilized as therapeutic and diagnostic agents.

The nature of the L group as a linker group is such that it may be varied widely without affecting the usefulness of the compounds of Formula I and Formula II, and the metal complexes thereof. Thus, L may be any suitable organic radical and may be, for instance, an optionally substituted aliphatic hydrocarbon chain, optionally interrupted by one or more hetero atoms selected from -0- or -S-or by one or more -NR ¹ - groups (where R' is a hydrogen atom or a C-l alkyl group) , -CONR'- groups, -NR'CO- groups, cycloaliphatic groups, aromatic groups, heteroaromatic groups, or a mixture thereof.

Yet another embodiment of the present invention includes the metal chelates of the conjugate of Formula

II. Preferably, the metals are chosen from the elements including copper, lead, indium, yttrium, bismuth, the lanthanides, gold, silver, and gallium. Such metal chelates may also be utilized as therapeutic and diagnos- tic agents.

Particularly preferred embodiments of the present invention involve metal chelates of the ligand of Formula II with the radioactive isotopes In-lll, Y-90, Bi-212, Pb- 202, Pb-212, Ga-66, Ga-67, Ga-68, and Cu-67. The metal chelate conjugated antibodies of this invention can be administered in vivo in any suitable pharmaceutical carrier. As noted earlier, a physiologic normal saline solution can appropriately be employed.

Often the carrier will include a minor amount of carrier protein such as human serum albumin to stabilize the antibody. The concentration of metal chelate conjugated antibodies within the solution will be a matter of choice. Levels of 0.5 mg per ml are readily attainable but the concentrations may vary considerably depending upon the specifics of any given application. Appropriate concen¬ trations of biologically active materials in a carrier are routinely determined in the art. The effective dose of radiation or metal content to be utilized for any application will also depend upon the particulars of that application. In treating tumors, for example, the dose will depend, inter alia, upon tumor burden, accessibility and the like. Somewhat similarly, the use of metal chelate conjugated antibodies for diag¬ nostic purposes will depend, inter alia, upon the sensing apparatus employed, the location of the site to be exam¬ ined and the like. In the event that the patient has circulating antigen in addition to those located at the site, the circulating antigens can be removed prior to treatment. Such removal of antigens can be accomplished, for example, by the use of unlabeled antibodies, or by plas apheresis in which the patient's serum is treated to removed antigens. The invention can be better illustrated by the use of the following non-limiting examples, all of which relate to the synthesis represented in Figure 1.

Example 1

Preparation of BOC-p-nitro phenylalanine trans-cvclo- hexyldiamine monoamide

The typical procedure used to prepare the active ester was to dissolve the BOC acid, N-hydroxysuc- cinamide, and EDC (48 mmol) in ethyl acetate ((400mL).

The mixture was stirred for 12 hours. The reaction solution was then filtered, and the filtrate was washed sequentially with saturated salt solution, 1M HCl, 5%

NaHCO,, and saturated salt solution (200 mL each). The organic layer was separated and dried over MgS0 ₄ - After

filtering, the solution was rotary evaporated to a solid. The solid was taken up in DMF (200 mL) and added dropwise to trans-l,2-diaminocyclohexane over a period of 18 hours. The precipitated diamide was filtered off, and the solu- tion was rotary evaporated to a thick oil. The residue was taken up in chloroform and washed, as above, to remove any of the starting materials. The chloroform solution was dried as before, filtered, and concentrated to a gel¬ like consistency. This material was poured onto a Buchner funnel and triturated with petroleum ether to leave the product as a light tan solid.

Example 2 Preparation of p-Nitrobenzyl-"CHX" diethylenetriamine

The BOC group was cleaved by stirring the amide (4.6 g) overnight in dioxane (300 mL) saturated with HC1. Addition of diethyl ether (200 mL) , followed by cooling to 4°C, added significant precipitate. The dihydrochloride was collected on a Buchner funnel under argon and vacuum dried. The amide dihydrochloride was suspended in THF (50 mL) in a three neck round bottom flask held in an ice bath. The flask was fitted with a condenser, thermometer, and a septum. Diborane/THF (6 eqv's) were injected into the flask, and the temperature was raised to 50°C and maintained there until the reduction was complete. The progress of the reaction was monitored by HPLC using a ten minute gradient of 100% 0.1M HOAc in water to 100% 0.1M HOAc in methanol. The column was a Waters DeltaPak C _.

After the reaction was finished, the solution was cooled to room temperature, and methanol (50mL) was added to decompose any excess hydride. The solution was taken to dryness on a rotary evaporator, and the residue was taken up in 100% ethanol (100 mL) . This solution was taken to dryness using a high vacuum rotary evaporator. Dioxane (150 mL) , previously saturated with HC1, was added to the solid and the suspension was refluxed for four hours. The final suspension was left at 4°C for 18 hours.

The product was collected on a Buchner funnel under argon and then vacuum dried.

Example 3 Preparation of p-Nitrobenzyl CHX DTPA The triamine (1.0 g, 2.49 mmol) was dissolved in

DMF (25 mL) with sodium carbonate (1.992 g) , and tert- butyl bromoacetate (2.915 g, 14.95 mmol) was added. The solution was heated to about 80°C overnight under argon, after which the reaction mixture was poured into H_0 (100 mL) and extracted with CH ₂ C1 (100 mL) . The organic layer was washed with water (3 x 100 mL) , separated, dried over MgSO. , filtered, and rotary evaporated to an oil. The oil was further concentrated to a thick oil by high vacuum rotary evaporation. A CI-MS of this oil indicated that the penta ester was by far the principal product (greater than 70%) .

The oil was treated with TFA (25 mL) overnight. The excess reagent was removed by rotary evaporation. HPLC revealed essentially two major peaks, 10.95 minutes and 11.9 minutes. The HPLC method was a gradient of 0.05M Et ₃ N/HOAc to 100% MeOH over 25 minutes. Preparative HPLC was performed to separate and collect the two peaks. After completion of the pre-HPLC, the HPLC buffer was removed by ion-exchange chromatography (AG50 Wx8 200/400 mesh H+ form) . Analytical HPLC of the two separated fractions indicated two separated pure products. After lyophilization, the two fractions were each treated with bis(trimethylsilyl) trifluoracetamide and EI-MS's were obtained. Each EI-MS gave the same M+ which in turn corresponded to the desired pentaacetic acid, each peak therefore being a separated pair of diastereomers now labeled a CHX-A or CHX-B.

Example 4 Preparation of p-Aminobenzyl CHX DTPA-A. -B Atmospheric hydrogenation of each fraction was performed using 100 mg of each nitro compound with 10% Pd/C (100 mg) at pH 8.5. The reaction was allowed to proceed until the H_ uptake had halted. The reaction

mixture was filtered on a fine frit with Celite 577. The filtrate was lyophilized to leave an off-white residue.

Example 5

Preparation of p-Isothiocyanatobenzyl CHX DTPA-A. -B

Each fraction was dissolved in H ₂ 0 (5mL) and treated with thiophosgene (20uL) in CHCl (lOmL) with maximum stirring under argon for two hours. The organic layer was removed by room temperature rotary evaporation, and the aqueous layer was lyophilized to leave an off- white solid. I.R. spectrum of each fraction showed a good, strong ban'd at 2100 cm ^" for the aryl SCN group.