IL114175A - Nitroheterocyclic boronic acid derivatives - Google Patents

Description

NITROHETEROCYCLIC BORONIC ACID DERIVATIVES The present specification relates to nitroheterocyclic boronic acid derivatives, and is divided from Israel Specification 96946.

Israel Specification 96946 is directed to boronic acid derivatives, diagnostic methods and kits containing the same, as described hereinafter, while the present invention is directed to novel nitro-heterocyclic compounds which are intermediates for the preparation of said boronic acid derivatives.

In order that the invention may be better understood and appreciated, description from Israel Specification 96946 is included herein, it being understood that this is for background purposes only, the subject matter of Israel Specification 96946 being specifically disclaimed and not forming a part of the present invention.

Radiolabelled, biochemically active groups are of increasing interest in the field of diagnostic imaging. Essentially, a biochemically active group is a metabolic substrate or inhibitor, or a molecule with an affinity for a specific receptor. Knowledge of certain properties, such as receptor binding or metabolism, involving various biochemically active groups suggests, at least in theory, that radiolabelled versions of such groups may be useful in imaging the function and/or condition of a specific organ, rather than merely the blood flow to that organ. An effective complex is one wherein the radionuclide and biochemically active group are stably bound to each other and further, wherein the complex behaves, or is "taken up," substantially as the free biochemically active group would behave .

Numerous attempts to prepare effective complexes of this nature have been reported. For example, Fowler, et al. ( "2-deoxy-2 [ 1βΓ]ΐluoro-D-glucose for Metabolic Studies: Current Status," Int. J. Appl. Radiat. Isot. , Vol. 27, pp. 663-668 (1986)) have investigated the radiolabelling of the metabolic substrate, deoxyglucose , with 18F for use in diagnostic imaging of the brain. Brain and lung imaging has also been attempted by Winchell et al. (J. Nucl. Wed., 1980, 21, p. 940-6, "Development of I-123-Labeled Amines for Brain •Studies: Localization of 1-123 Iodophenylalkyl Amines in Rat Brain" and J. Nucl . Med. , 1980, 21, p. 947-52, "N-Isopropyl- [ 1231 ]p-Iodoamphetamine : Single-Pass Brain Uptake and Washout; Binding to Brain Synaptosomes ; and Localization in Dog and Monkey Brain") who report radiolabeling of amphetamines, known to interact with specific receptors, with 123I. The radio-iodinated amphetamine known as "spectamine" is currently marketed for brain imaging.

Free fatty acids are primary substrates of the normally perfused myocardium and, as such, are viewed as potentially useful in studying free fatty acid metabolism via the beta-oxidation pathway.. Accordingly, van der Wall et al.

(Eur. J. Nucl. Med., 1986, 12, p. S11-S15, "Myocardial imaging with radiolabeled free fatty acids: Applications and limitations") have studied free fatty acid labeled with positron emitting isotopes, e.g., llC, 13N and 150, as well as with the gamma-emitting isotope 1231. Additionally, Jones et al. (J. Nucl. Med., 1988, 29(5), p. 935, "Synthesis of a Novel [Tc99m] -Diaminodithiol-Fatty Acid (TcN2S2FA) Complex and Its Evaluation as a Myocardial Imaging Agent") have disclosed attempts to image normal myocardium utilizing fatty acids with technetium-99m (99mTc).

The discovery of specific estrogen receptors in breast carcinoma has led to work in the radiolabeling of various steroids, e.g., estrogens or derivatives thereof, e.g., estradiols. It is believed that a radiolabeled estrogen may be able to indicate receptor levels and help determine types and levels of therapy for breast carcinoma. In this regard, Jagoda et al . , (J. Nucl. Med., 1984, 25, p. 472-7, "[125I]-17- Iodovinyl 11-Methoxyestradiol : In vivo and In vitro Properties of a High Affinity Estrogenic) Receptor Radiopharmaceutical") have studied 1251 labeled methoxy estradiol for such diagnostic uses.

Gibson et al . (Biochem Pharm. , Vol. 32, No. 12, p. 1851-56, 1983, "Differences in Affinities of Muscarinic Acetylcholine Receptor Antagonists for 15 Brain and Heart Receptors" and J. Nucl . Med. , Vol.

, No. 2, p. 214-222, February 1984, "The Characteristics of 1-125 4-IQNB and H-3QNB In vivo and In vitro") have studied the substrates for muscarinic receptors, e.g. 3-guinuclidinyl 0 benzilate (QNB) and derivatives thereof, radiolabeled with 1251 and 3H in heart and brain tissue.

As reported by Martin et al. ("Enhanced Binding of the Hypoxic Cell Marker [3H] Fluoro- 5 misonidazole" , J. Nucl. Med. , Vol 30, No. 2, 194-201 (1989)) and Hoffman et al. ("Binding of the Hypoxic Tracer [H-3] Misonidazole in Cerebral Ischemia", Stroke, 1987, 18, 168), hypoxia-mediated nitro-heterocyclic groups (e.g., nitroimidazoles , 0 and derivatives thereof) are known to be retained in tissue in the body which is hypoxic, i.e., deficient in oxygen. Hypoxic tissue in the brain or heart typically follows ischemic episodes produced by, for example, arterial occlusions or by a combination of increased demand and insufficient flow. Additionally, Koh et al . , (J. Nucl . Med., 19Θ9, 3_0, p. 789, "Hypoxia Imaging of Tumors Using [ F-18 ] Fluoromisonidazole" ) have attempted diagnostic imaging of tumors using a nitroimidazole radiolabeled with 18F.

The above-mentioned attempts at diagnostic imaging with various radiolabeled biochemically active groups have provided less than ideal results to this point. For example, the positron emitting isotopes are cyclotron produced and require extensive equipment for imaging which is not widely available. Similarly, 123i has a thirteen hour half life and is expensive to produce.

Further, the complexes with fatty acids have not demonstrated the characteristics of the free fatty acids in myocardial uptake. Finally, the tritium labeled nitroimidazoles are beta-emitting nuclides useful only for autoradiographic studies and not suitable for diagnostic imaging.

Radiolabeled complexes of biochemically active groups which retain the biochemical behavior and affinity of such groups, and which are labeled with a suitable, easy-to-use radionuclide would be a useful addition to the art.

In accordance with the invention of Israel Specification 96946, boronic acid adducts of rhenium dioxime and technetium-99m dioxime complexes are bonded to a biochemically active group and are useful, for example, as diagnostic imaging agents in the case of technetium-99m and as agents for radiotherapy in the case of rhenium radionuclides. These novel complexes are represented by the formula I X(Y3 )z, wherein M is technet um-99m or rhenium. Unless otherwise noted, rhenium includes 186Re and 188Re radionuclides, including mixtures thereof, and may also include amounts of ,85Re and 187Re. In formula I, and throughout the specification, the symbols are as defined below X is an anion; Y is a vicinal dioxime having the formula II HO-N=C—C=N-OH or a pharmaceutically acceptable salt thereof, and Ri and R2 are each independently hydrogen, halogen, alkyl, aryl, amino or a 5- or 6-membered nitrogen or oxygen containing heterocycle, or together Rx and R2 are -(CRe 9)n- wherein n is 3, 4, 5 or 6 and R8 and R9 are each independently hydrogen or alkyl; Z is a boron derivative having the formula III B-(Aa)p-R3 wherein R3 is, or contains, a biochemically active group, and wherein (Ax ) is absent when p = 0 or is a spacer group when p is > 1.

As shown, in the case where the biochemically active group may be inhibited in its action by the close proximity of the remainder of the complex, it (the biochemically active group) can be bound to the complex via the spacer or linking group, (Aj ) .

This spacer group can be any chemical moiety which can serve to physically distance, or otherwise isolate, the biochemically active group at R3 from the rest of the complex of formula I. For example, in the spacer group, wherein p is one, Aj , or the various Aj units in forming a straight or branched chain if p > 1, are independently selected from ~CH2 ~ , —CHR — , -CR4R5 — , —CH=CH— , —CH=CR4 — , —CR4=CR5— , -C≡C-, cycloalkyl, cycloalkenyl , aryl, heterocyclo, 0 II oxygen, sulfur, -C-, -ΝΉ- , -HC=N- , -CR4=N- , - R4 - , -CS-; wherein R4 and R5 are independently selected from alkyl, alkenyl, alkoxy, aryl, 5- or 6-membered nitrogen or oxygen containing heterocycle, halogen, hydroxy or hydroxyalkyl .

In considering the various spacer groups known in the art, it is understood that p could be any convenient value depending upon the design choices for the desired complex. Preferably, p is < 100 and most preferably p 20.

Listed below are definitions of the terms used to describe the complexes of this invention. These definitions apply to the terms as they are used throughout the specification (unless they are otherwise limited in specific instances) either individually or as part of a larger group.

The terms "alkyl", "alkenyl" and "alkoxy" refer to both straight and branched chain groups. Those groups having 1 to 10 carbon atoms are preferred.

The term "aryl" refers to phenyl and substituted phenyl. Preferred are phenyl and phenyl substituted with 1, 2 or 3 alkyl, haloalkyl, aminoalkyl, alkylaminoalkyl , dialkylaminoalkyl , alkoxy, alkoxyalkyl, halogen, amino, hydroxy, or formyl groups.

The terms "halide" , "halo" and' "halogen" refer to fluorine, chlorine, bromine and iodine.

The expression "5- or 6-membered nitrogen containing heterocycle" refers to all 5- and 6-membered rings containing at least one nitrogen atom. Exemplary aliphatic groups are dehydro derivatives of a compound having the formula wherein m is 0 or 1 and A is -0-, -N-R6 , -S- or -CH-R6 wherein R6 is hydrogen, alkyl, aryl or arylalkyl. Such groups include pyrrolidinyl , piperidinyl, morpholinyl, piperazinyl, 4-alkyl-piperazinyl, 4-alkylpiperidinyl , and 3-alkyl-pyrrolidinyl groups. Also included within the expression "5- or 6-membered nitrogen containing heterocycle" are aromatic groups. Exemplary aromatic groups are pyrrolyl, imidazolyl, oxazolyl, pyrazolyl, pyridinyl, and pyrimidinyl groups. The above groups can be linked via a hetero atom or a carbon atom.

The expression "5- or 6-membered nitrogen or oxygen containing heterocycle" refers to all 5-and 6-membered rings containing at least one nitrogen or oxygen atom. Exemplary groups are those described above under the definition of the expression "5- or 6-membered nitrogen containing heterocycle" . Additional exemplary groups are 1.4-dioxanvl and furanyl .

For those complexes of said invention wherein M is rhenium, the biochemically active group is bound to complexes as defined in U. S. 4,871,836 issued October 3, 1989. For those complexes of formula I where M is Tc-99m, the biochemically active group is bound to a complex as defined in U. S. 4,705,849, issued November 10, 1987. The present invention provides complexes comprising radiolabeled biochemically active groups. A biochemically active group suitable for use in the present invention is any metabolic substrate or inhibitor, or a molecule with an affinity for a specific receptor/ It is understood that for the purpose of this invention the category of biochemically active groups which are molecules with an affinity for specific receptor sites is limited to those groups capable of being incorporated into the complexes of formula I by the methodology described hereinafter.

Examples of suitable biochemically active groups include, but are not limited to, hypoxia-mediated nitro-heterocyclic groups, amphetamines, steroids (such as an estrogen or estradiol), sugars (e.g. glucose derivatives), fatty acids, barbiturates, sulfonamides, monoamine oxidase substrates and inhibitors, antihypertensives, substrates for muscarinic receptors (e.g., 3-quinuclidinyl benzilate), and substrates for dopamine receptors (e.g., spiperone).

Complexes of said invention have not been heretofore disclosed and are useful in that they utilize properties, e.g., receptor binding, metabolism, etc., of a particular biochemically active group, to provide imaging or treatment of a particular site. The complexes of said invention, wherein M is 99mTc, provide highly effective, relatively easy to use, diagnostic imaging products which are characterized by a covalent bond between the radionuclide complex and the biochemically active group, while substantially retaining the uptake properties of the free biochemical group. It can be appreciated that typical examples of diagnostic uses for the complexes of the present invention, when M is 99mTc, include, but are not limited to, imaging of hypoxic tissue, e.g., in the heart, brain, lungs or in tumors when the biochemically active group is a nitro-heterocyclic group trapped by hypoxia-mediated reduction of the nitro moiety (hereinafter referred to as "hypoxia-mediated nitro-heterocyclic group" ) ; imaging of the brain and lungs when the biochemically active group is a lipophilic amine-containing compound, e.g., an amphetamine; imaging of the brain, heart or tumors when the biochemically active group is a sugar (e.g., a glucose derivative); imaging of the heart when the biochemically active group is a fatty acid; and imaging of steroid receptor sites when the biologically active group is a steroid (e.g., an estrogen for imaging breast carcinoma) .

Additionally, said invention provides stably bound complexes when M is Re for radiotherapeutic indications. For example, the above-mentioned U.S. Patent 4,871,836, issued October 3, 1989, describes Re complexes for radiotherapy. Re complexes of said invention which include estradiols can be used in the treatment of breast carcinoma. Also, to the extent that hypoxic tissue is known to be present in tumors, Re complexes of said invention wherein the biochemically active group is a hypoxia-mediated nitro-heterocyclic group are suitable for radiotherapy. The compounds of said invention when is Re for use in radiotherapy can be injected into humans and concentrate at the desired site. This allows for the targeting of radionuclides to the desired sites with great specificity. It is understood, however, that radiotherapy will only be possible in those areas where a sufficient quantity of interacting sites (i.e., estrogen receptors or hypoxic tissue) are present so as to provide therapeutic levels of rhenium to the area needing treatment.

Examples of hypoxia-mediated nitro-heterocyclic groups, (i.e., nitro-heterocyclic groups trapped by hypoxia-mediated reduction of the nitro moiety) , in addition to the Koh, et al. and Hoffman, et al. references mentioned above, include those described in G.L. Kedderis, et al., "The Metabolic Activation of Nitro-Heterocyclic Therapeutic Agents," Drug Metabolism Reviews, Vol. 19, No. 1, pp. 33-62 (1988); G.E. Adams, et al., "Hypoxia Mediated Nitro-Heterocyclic Drugs in the Radio- and Chemotherapy of Cancer," Biochem. Pharmacology, Vol. 35, No. 1, pp. 71-76 (1986); D.M. Brown, et al., "Structure-Activity Relationships of 1-Substituted 2-Nitroimidazoles : Effect of Partition Coefficient and Sidechain Hydroxyl Groups on Radiosensitization in Vitro, " Rad. Research, Vol. 90, pp. 98-108 (1982); G.E. Adams, et al., "Structure-Activity Relationships in the Development of Hypoxic Cell Radiosensitizers , " Int. J. Radiat. Biol., Vol. 35, No. 2, pp. 133-150 (1979); and G.E. Adams, et al., "Structure-Activity Relationships in the Development of Hypoxic Cell Radiosensitizers," Int. J. Radiat. Biol., Vol. 38, No. 6, pp. 613-626 (1980). These all disclose various nitro-heterocyclic compounds suitable for use at R3 in the complexes of said invention, and are incorporated herein by reference. These compounds comprise a nitro-heterocyclic group which may include a sidechain A^, which can serve as the spacer group linking the nitro-heterocyclic portion to the boron atom and the rest of the complex of formula I of said invention.

When the biochemically active group is a hypoxia-mediated nitro-heterocyclic group, the spacer-R3 portion of the complex can be represented by: the ring portion being a 5- or 6-membered cyclic or aromatic ring, wherein n is the total number of substitution positions available on the 5- or 6-membered ring; the one or more R substituents are independently selected from hydrogen, halogen, alkyl, aryl, alkoxy, oxa-alkyl, hydroxyalkoxy , alkenyl, arylalkyl, arylalkylamide , alkylamide, alkylamine and ( alkylamine) alkyl ; Xj can be nitrogen, oxygen, sulfur, -CR= or -CRR- ; and (Ax ) can be absent in which case the R3 group of formula IV, IV* or IV" is linked to the rest of the complex of this invention via a nitrogen or carbon atom, or (Ax ) is the linking group and (hi ) can be as defined above.

The references, above, regarding hypoxia-mediated nitro-heterocyclic groups serve to illustrate that the present thinking in the art is that the reduction potential of the nitro-heterocyclic group directly affects its retention in hypoxic tissue. The spacer group, (A:)p, may therefore (in the case where R3 is a hypoxia-mediated nitro-heterocyclic group) be selected not only according to its capacity to distance R3 from the rest of the complex, but also in accordance with its effect on the reduction potential of the hypoxia-mediated nitro-heterocyclic group.

Similarly, the present knowledge in this art provides that one skilled in the art would understand to select the values and/or positions for Aj , R, Xi and -N02 in the groups of formula IV, IV and IV" according to their known effects on the reduction potential as pointed out in the literature .

Preferred hypoxia-mediated nitro-hetero- cyclic groups are 2-, 4- and 5-nitroimidazoles which can be represented by and nitrofuran and nitrothiazole derivatives, such Exemplary groups (including (At ) spacers) include, but are not limited to, CH2-0-C-NH2 -CH2 -N N / N02 Most preferred when R3 is a hypoxia-mediated nitro heterocyclic group are 2-nitroimidazoles and-derivatives thereof.

When the biochemically active group at R3 is a steroid it is understood that either a steroid, a substituted steroid derivative or a non-steroidal derivative can be employed provided that the R3 group chosen has an affinity for the steroid receptor. For example, when R3 is estradiol OH the (Aj ) linking group, or the boron atom in the case where p = 0, can be at any available position on the molecule but preferably Ai is linked either to an atom in the B ring or to an atom in the D ring. Additionally, the estradiol molecule may be substituted at available positions by one or more of R, wherein R is as defined above. Alternatively, the steroid molecule can be replaced by a nonsteroidal diol with a known affinity for the estrogen receptor, such as wherein (Aj ) and R are as defined above.

When the biochemically active group is a substrate for a muscarinic receptor, the spacer-R3 portion of the complex can be represented by wherein (Ai ) and R are as defined above and R 1 is a tertiary or quaternary amine, such as 3-quinuclidinol or substituted 3-quinuclidinol.

All of the examples and the following process description in the case where M is rhenium involve the use of "carrier rhenium" except as otherwise noted. The phrase "carrier rhenium" means that the rhenium compounds used contain -7 non-radioactive rhenium at concentrations of 10 M to 10"5M.

Preparation of the complexes of said invention wherein M is rhenium can be accomplished using rhenium in the +3, +4, +5 or +7 oxidation state. Examples of compounds in which rhenium is available in the +3 oxidation state are ReCl3 ( CH3CN) (PPh3 )2 and [ Re2 Cl b ] ( NBu4 ) 2 wherein Ph = phenyl and Bu = butyl. Re(IV) is available as K2ReCle and Re(VII) is available as NH4Re04 or KRe04. Re(V) is available as ( ReOCl4 ] ( NBu4 ) and [ReOCl4 ] ( AsPh4 ) and as ReOCl3 ( PPh3 ) 2 and as ReO (pyridine),,®. Other Re ( 111 ) , Re(IV), Re(V), Re(VII) reagents known to those skilled in the art can also be used.

Preferably, the Re complexes of said invention are prepared using Re intermediate complexes of the formula V ReX(Y)3 (wherein X and Y are as defined above) which have been described in EP 91/441491, entitled "RHE IUM TRIS DIOXIME COMPLEX". By reacting intermediates of formula V with a boronic acid derivative of the formula the rhenium complexes of said invention are provided. Intermediates of formula V can be prepared using Re(III), Re(IV), Re(V) or Re(VII) reagents as described above, combined with a source of anion moiety (X), and a vicinal dioxime of formula II. This mixture should be reacted/heated at about 25°C to 100°C for about 5 minutes to 8 hours. If Re(IV), Re(V) or Re(VII) are used, known methodologies for adding a reducing agent sufficient to reduce these starting materials to Re(III) should be employed.

Preparation of the complexes of said invention wherein M is technetium-99m can best be accomplished using technetium-99m in the form of the pertechnetate ion. The pertechnetate ion can be obtained from commercially available technetium-99m parent-daughter generators; such technetium is in the +7 oxidation state. The generation of the pertechnetate ion using this type of generator is well known in the art, and is described in more detail in U. S. Patent No. 3,369,121 and 3,920,995. These generators are usually feluted with saline solution and the pertechnetate ion is obtained as the sodium salt.

A method to prepare ^"^Tc complexes, which is an alternative method to prepare Re complexes of this invention, includes the combining of the Re(III), Re(IV), Re(V), Re(VII) or pertechnetate ion (in the form of a salt) with a source of anion, a boronic acid derivative having formula VI or a pharmaceutically acceptable salt thereof, (wherein R7 and R7 ' are each independently hydrogen, alkyl or aryl, or where R7 and R7 ' taken together are -(CR8R9)n- wherein n is 2-6) and a dioxime having the formula f1 *2 II HO-N=C—C=N-OH , or a pharmaceutically acceptable salt thereof.

Compounds of formula VI wherein R3 is a hypoxia-mediated nitro-heterocyclic group as defined in formula IV, IV or IV", that is, N02 are novel intermediates and are the subject matter of the present invention.

More specifically, the present invention provid nitro-heterocyclic compound of the formula: NO- or wherein the ring portion is a 5- or 6-membered cyclic or aromatic ring; n is the total number of substitution positions available on said 5- or 6-membered ring; said one or more R groups are independently hydrogen, halogen, alkyl, aryl, alkoxy, oxa-alkyl, hydroxyalkoxy, alkenyl, arylalkyl, arylalkylamide , alkylamide, alkylamine and ( alkylamine) alkyl; Xj is nitrogen, sulfur, oxygen, -CR= or -CRR- ; and (A: ) can be absent when p is zero in which case said ring is linked to the boron atom via a nitrogen or carbon atom, or (AjJ^, when p is an - 20 - 114,175/2 between said ring and the boron atom; wherein Alf or the various Aa. units in forming a straight or branched chain if p > 1, are independently selected from -CH2-, -CHR4-, -CR4RS-, -CH=CH=, -CH=CR4-, -CR4=CRS-, -C≡C- , cycloakyl, O II cycloalkenyl, aryl, heterocyclo, oxygen, sulfur, -C-, -NH-, -HC=N-, -CR4=N, -NR4- , -CS-; wherein R4 and Rs are independently selected from alkyl, alkenyl, alkoxy, aryl, 5- or 6-membered nitrogen or oxygen containing heterocycle, halogen, hydroxy or hydroxyalkyl ; and wherein Rv and Rv' are each independently hydrogen, alkyl, or aryl, or where Rv and R7' taken together are -(CReRs)2-6- and Ra and R«, are independently hydrogen or alkyl.

In preferred embodiments of the present invention, said ring portion is a 2-, 4-, or 5-nitroimidazole, a nitrofuran or a nitrothiazole, including derivatives thereof.

Preferably, said is absent or is selected from alkyl, alkyl with one or more ether linkages, hydroxyalkyl, hydroxyalkoxy, alkenyl, arylalkyl, arylalkylamide , alkylamide, alkylamine and (alkylamine) alkyl.

Especially preferred according to the present invention is a compound wherein said ring portion is a 2-nitroimidazole ; - 21 - 114,175/2 (Ai) is selected from -(CH2)2_3-, 0 -CH2-CH=CH-CH2-, -(CH2 ) ^-C-NH- < CH2 )1-3-, OCH2-, -(A3-NH-A3 ' )1.3- wherein A3 and A31 are the same or different alkyl .

Preferred compounds of the present invention are l-( 2-nitroimidazole) -benzylboronic acid; 4-(2-nitro-imidazolyl ethyDphenyl boronic acid; 2-nitroimidazolyl-N].-[ 2-propenyl]-3-boronic acid (Bpropen 02 ) ; 2-nitroimidazolyl-Ni-propyl-3 -boronic acid (BpropN02); 1- ( 4-nitroimidazole ) -benzylboronic acid (BB4N02); (R) -l-azabicyclo[ 2 , 2 , 2 ]oct-3-yl- ( R) -α-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (R,R-QNB boronic acid); ( S) -l-azabicyclo[ 2 , 2 , 2 ]oct-3-yl- ( R) -a-hydroxy-α- ( 4 ) -phenylboronic acid-a-phenylacetate (R,S-QNB boronic acid); ( S ) -l-azabicyclo[ 2 , 2 , 2 ]oct-3-yl- ( S ) -a-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (S,S-QNB boronic acid); and (R) -l-azabicyclo[ 2,2, 2 ]oct-3-yl- ( S ) -a-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (S,R-QNB boronic acid) .

These can be prepared using known methodology. For example, a boronic acid derivative of the formula VIII -L here L is a leaving group, e.g., halogen, etc. an be coupled with a compound of the formula in a solvent, e.g., dimethylforma ide and in the presence of a base, e.g., potassium carbonate.

This is the preferred method for preparing the novel intermediates of formula VII.

Preferably, the novel intermediates of formula VII1 and VII" can be prepared by coupling a compound of the formula with a compound of the formula or in a solvent and in the presence of a base.

The source of the anion moiety (X) can be water or it can be an acid or salt which dissociates to release an appropriate anion.

Exemplary anionic moieties are hydroxyl, halide, 9 Q isothiocyanato (N=C=S ) and thiocyanato (S-C=N ). The preferred anionic moieties are the halides, and chloride is the most preferred halide. If the source of the anion is not water, the source should be present in an appropriate concentration to compete effectively with any water that may be present during the reaction. It has been found that the source of anion should be present in the reaction mixture in a concentration of about 0.1 to about 2.0 molar.

The boronic acid derivative of formula VI, VII, VII' or VII" should preferably be present in a concentration of about 5 to 400 millimolar. The dioxime of formula II should preferably be present in a concentration of about 9 to 250 millimolar. 9m The formation of the TC complexes proceeds best if the mixture of pertechnetate ion, source of anion, boronic acid derivative, and dioxime is heated at about 25°C to 100°C for about 5 minutes to about 3 hours. The reaction is preferably run in an aqueous medium or aqueous alcohol mixture at a pH of less than, or equal to, about 5. Re complexes starting with Re(III), Re (IV), Re(V) or Re(VII) can also be formed using this methodology. However, as mentioned previously, for Re complexes, and also for Tc-99m complexes wherein the R3 or (Aj ) group may be sensitive to the above-described temperature and pH parameters, it is preferable to react an intermediate complex MX(Y)3 with a boronic acid derivative of formula VI, VII,' VII' or VII". This can be done in an aqueous medium or aqueous alcohol mixture at about 25-100°C for about 5 minutes to 8 hours at a pH <5.

If pertechnetate or Re (IV), Re(V) or Re (VI I) containing compounds are employed, then the reaction mixture should also contain a reducing agent.

Stannous ion is the preferred reducing agent, and can be introduced in the form of a stannous salt such as a stannous halide (e.g., stannous chloride or stannous fluoride). The reducing agent should be present in a concentration of about 10 millimolar to 150 millimolar.

With specific reference now to the examples and figures in detail, it is stressed that the particulars described and shown are by way of example and for purposes of illustrative discussion of the preferred embodiments of the present invention only, and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the invention. In this context, it is to be noted that only subject matter embraced in the scope of the claims appended hereto, whether in the manner defined in the claims or. in a manner similar thereto and involving the main features, as defined in the claims, is intended to be included in the scope of the present invention, while subject matter of Israel Specification 96946, although described and exemplified to provide background and better understanding of the invention, is not intended for inclusion as part of the present invention.

Exemple 1 [ 99Tc( chloride ) ( dimethylglyoxime )3 [4- [2- [ ( 1-methyl-ethyl ) amino 1 ropy 1 1 pheny1 ]boron ]PF6 0.20429 g (1.76 mmol) of dimethylglyoxime and 0.13508 g (0.6 mmol) of [4- [2- [ ( 1-methylethyl )-amino jpropyl ]phenyl ]boronic acid were dissolved in 20 mL of ethanol and 5 mL of water. 0.09035 g (0.5 mmol) of ammonium pertechnetate dissolved in 6 mL of 3 M HCl was added. While stirring, 0.21492 g (1.1 mmol) of stannous chloride dissolved in 5 mL of 4 M HCl was added dropwise over 5 minutes. The solution became an intense orange-brown in color. 20 mL of water were added and the reaction mixture was stirred at reflux for 2 hours. The reaction mixture was exhaustively extracted with dichloromethane , the combined CH2C12 fractions were dried through anhydrous sodium sulfate, and concentrated by rotoevaporation. Methanol, 4 M HCl and NH4PF6 in methanol were added to the CH2C12 concentrate.

The desired product, as the PF6~ salt, precipitated on evaporation. The orange precipitate was collected by filtration, washed with water and vacuum dried. Yield: 0.122 g (31%).

Elemental analyses calc'd for TcClC24H39 706BPF6 ¾ CH2 Cl 2 ' C, 34.43; H, 4.68; N, 11.48; Found: C, 34.25; H, 4.45; N, 11.66.

E ample 2 99mTc ( chloride ) ( dimethylglyoxime )3 [4- [2- [ ( 1-methyl-ethyl ) amino] propyl] phenyl] boron Into a 5 mL siliconized serum vial were measured 1.7 mg of dimethylglyoxime, 7.0 mg of [4- [ 2- [ ( 1-methyl -ethyl ) amino ]propyl ] phenyl jboronic acid, 20 mg of citric acid, 2 mg of DTPA, 100 mg of NaCl, and 50 g of SnCl2 (in 4 M HC1) in a total volume of 0.5 mL of saline. 0.5 mL of 99mTc04~ generator eluent was added and the mixture was heated at 100°C for 15 minutes, yielding 76% of the desired product as determined by HPLC. The product was purified chromatographically to give the product with 91% purity.

Example 3 Biodistribution Results for Amine-substituted Boron complexes, 99mTc ( chloride )( dimethylglyoxime )aB-R (wherein R is or contains an amine) Since it is well known that lipophilic amines demonstrate high lung uptake through specific binding, the lung uptake of a series of (BATO) complexes containing amine substituents in the boronic acid "cap", including the complex described in Example 2, were determined in rats. The other complexes listed were prepared using the methodology described in Example 2. Lung uptake at 5 and 60 minutes post I.V. administration of these compounds was noted. Table 1 below shows the lung uptake of the amine-containing complexes.

Table 1 Amine-Containinq % Injected Dose in Lungs at 5 min. and 60 min. Post -injec • % in Dioxime Amine 5 min . P.I.

DMG1 4- [2- [ ( 1-methylethyl ) amino1propyl ]phenyl boronic acid 3. 25 II N, N-Dimethyl-p-aminomethylphenylboronic acid 1. 05 II N-Methyl-N-phenethyl-p-aminomethylphenylboronic acid 10. 59 II N-Isopropyl-p-aminophenylphenylboronic acid 1. 49 1 II N, N-Di-isopropyl-p-aminomethylphenylboronic acid 0. 98 II p-(N,N-Diisopropyl-l-aminoethyl )phenylboronic acid 3. 37 'DMG = Dimethylglyoxime Table 1 (cont'd) Amine-Containinq % Injected Dose in Lungs at 5 min. and 60 min. Post -injecti % in L Dioxime Amine 5 min . P.I.

CDO2 N, N-Dimethyl-p-aminomethylphenylboronic acid 1. 15 •1 N-Met yl-N-phenethyl-p-aminomethylphenyl- boronic acid 4. 76 II N-Isopropyl-p-aminophenylphenylboronic acid 3. 07 II N, N-Di-isopropyl-p-aminomethylphenylboronic acid 5. Θ9 II p-(N,N-Diisopropyl-l-aminoethyl )phenylboronic acid 3. 12 II N-Ethyl-N-isopropyl-p-aminomethylphenylboronic acid 5. 59 2 CDO = 1 , 2-Cyclohexanedione dioxime Example 4 99Tc( chloride ) (dimethylglyoxime )3 (estradiol boron ) 0.02796 g (0.058 mmol ) of 99Tc ( chloride ) -dimethylglyoxime )3 was dissolved in 10 mL of acetonitrile . While stirring, 0.02449 g (0.072 mmol) of estradiol boronic acid, [ 17a (E )-3 , 17-dihydroxy-1 ,3,5 ( 10 )-estratrien-17-yl ] ethenyl-boronic acid, was added as a solid. 2 mL of 1 M HCl were added and the reaction mixture was stirred with gentle heating for 1 to 2 hours.

Addition of 1 M HCl (3 to 5 mL) resulted in the precipitation of the product. The product was recrystallized from acetonitrile/1 M HCl. Yield: 0.022 g (48%).

Elemental analyses calc'd for: TcClC32H4 SN608B H H20: C, 48.27; H, 5.78; N, 10.56; Found: C, 48.26; H, 5.70; N, 10.50.

. Example 5 ( chloride ) dimethylglyoxime )3 (estradiol boron) Into a 5 mL siliconized serum vial were measured 2.0 mg of dimethylglyoxime, 2.2 mg of estradiol boronic acid, 20 mg of citric acid, 100 mg of NaCl and 100 ug of SnCl2 (in 4 M HCl) in a total volume of 0.6 mL of 33% ethanol/saline. 0.5 mL of 99mTc04~ generator eluent was added and the mixture was heated at 100°C for 15 minutes, yielding 70% of the desired compound as determined by HPLC.

ExajTple 6 99m '99 Tc(chloride) ( dimethylglyoxime ) 3 (estradiol boron) of known specific activity for in vitro estrogen receptor binding studies Samples were prepared containing both "Tc 99m_ and TC in order to determine the specific activity (Ci/mmol) accurately. Samples were prepared in the following manner: 2 mg of estradiol boronic acid, 0.2 mL of dimethylglyoxime (10 mg/mL of ethanol ) , 0.2 mL of citric acid (100 mg/mL of H20), 0.2 mL of saturated NaCl (in H20), 0.100 mL of NH4"Tc04 (3.66 x 10"4 M in H20) and 0.1 mL to 0.5 mL of 99mTc04" (eluent from a Mo99/Tc99m generator), to give the desired specific activity, were combined in a 5 mL siliconized vial. 10 L of SnCl2 (0.100 g dissolved in 1 mL of cone. HC1 and diluted to 4 mL with H20) were added to the reaction vial. The sample was heated for 15 minutes at 100°C, cooled for 5 minutes and purified chromatographicaily (PRP-1 resin) to yield the product in >95% purity.

Example 7 In vitro estrogen receptor binding studies using 99m/99Tc ^ chioride ) dimethylglyoxime ) 3 (estradiol The methods used for the receptor binding studies have been previously described by E. M. Jagoda et al., J. Nucl . Med. 1984, 25 472-7. " [ 125 I ]-17-Iodovinyl-ll-Methoxyestradiol : In Vivo and In Vitro Properties of a High Affinity Estrogen Receptor Radiopharmaceutical". Receptor binding studies using cytosolic preparations of isolated rat uteri from 20-25 day old female rats were performed to determine the affinity of the technetium labeled estradiol for the estrogen receptor. Preparations of the compound ranged in specific activity from 400 to 2000 Ci/mmol and the specific binding ranged from 10-30% of the total bound activity.

Example 8 TcCl(dimethylglyoxime)3 (QNB-boron) of known specific activity for in vitro muscarinic receptor binding studies 99 Samples were prepared containing both Tc and 99mTc in order to determine the specific activity (Ci/mmol) accurately. Samples were prepared in the following manner: 2 mg of 3-Quinuclidinyl- (4-boronobenzilate ) (QNB-boronic acid prepared as described by G. W. Kabalka et al., Nucl. Med. Biol. 1989, 16(4), 359-360), 0.2 mL of dimethylglyoxime (10 mg/mL of ethanol), 0.2 mL of citric acid (100 mg/mL of H20), 0.2 mL of saturated NaCl (in H20), 0.1 mL of DTPA (20 mg/mL of 0.5 M NaOH), 0.2 mL of gamma-cyclodextrin (25% w/v H20), 0.100 mL of NH499Tc04 (3.66 x 10"4 M in H20) and 0.1 to 0.5 mL of 99mTc04~ (eluent from a Mo99/Tc99m generator), to give the desired specific activity, were combined in a 5 mL siliconized vial. 10 yiL of SnCl2 (0.100 g dissolved in 1 mL of concentrated HC1 and diluted to 4 mL with H20) were added to the reaction vial. The sample was heated for 15 minutes at 100°C, cooled for 5 minutes and purified chromatographically (PRP-1 resin) to yield the product in 90-95% purity.

Example 9 In vitro muscarinic receptor binding studies using 99m/99Tc ( chloride ) (dimethylglyoxime).-, (QNB boron) The methods used for the receptor binding studies have been previously described by R. E. Gibson, W. J. Rzeszotarski , W. C. Eckelman, E. M . Jagoda, D. J. Weckstein, R. C. Reba, Biochemical Pharmacology, 1983, 32(12), 1851-1856. Receptor binding studies using rat caudate putameri isolated from rat brain were performed to determine the affinity of the technetium labeled QNB for the muscarinic receptor. Preparations of the compound ranged in specific activity from 600-1000 Ci/mmol and the specific binding ranged from 5-20% of the total bound activity.

Example 10 Preparation of l-(2-Nitroimidazole)-benzylboronic acid A. Preparation of p-tolylboronic acid p-Bromotoluene (17.1 g, 0.1 mole) in 150 mL of ether was added dropwise into a mixture of magnesium (2.5 g, 0.105 mole) in 30 mL of ether in a 200 ml reaction vessel. The reaction mixture was stirred overnight at room temperature. The dark brown solution was transferred into an addition funnel via a transfer needle, by nitrogen gas pressure.

This Grignard reagent was added dropwise over a period of 1.5 hours into a solution of trimethylborate (10.4 g, 0.1 mole) in 200 mL of ether at -78°C under nitrogen gas. After stirring overnight at ambient temperature, the resultant off-white reaction mixture was hydrolysed with 200 mL of water and acidified with 35 mL of 3N sulfuric acid. The aqueous layer was extracted with ether (4 x 80 mL). The combined organic layer was washed and dried over sodium sulfate. Removal of solvent afforded a white solid which was recrystallized from water. Yield 6.1 g (45%), m.p. 251-256°C (Lit. 259°C) 1H MR (DMSO) δ 2.25 (s, 3H,-CH3); 7.12 and 7.64 (d, 4H, ArH); 7.86 (s, 2H, -BOH) .

B . p-bromomethylbenzene boronic acid -2 mL of bromine solution (2.4 g, 1.5 x 10 mole) in 20 mL of carbon tetrachloride was added to a solution of p-tolylboronic acid (2.0 g, 1.47 x 10 mole) in 40 mL of carbon tetrachloride. The reaction was initiated by illumination with a 150 Watt light bulb. The bromine color faded in 5 minutes and the remaining bromine solution was added over 15 minutes. A solid product precipitated during bromine addition. The solid was filtered and crystallized from chloroform. washed with water, dried, concentrated and distilled under vacuum. Yield 6.0 g (95%), b.p. 115-117°C/0.7 mm, M.S. 314 and 316(m/e) *H NMR (CDC13), 0.05 (s, 6H), 0.9 (s, 9H), 2.8 (t, 2H), 3.85 (t, 2H) and 7.5 (AB q, 4H).

B. Preparation of 4-(2-hydroxy ethyl )phenyl boronic acid To a suspension of magnesium (0.264 g, 11 mmol) in dry tetrahydrofuran (10 ml) under nitrogen gas was added dropwise over ½ hour the t-butyl dimethyl silyl ether of 4-bromophenyl ethyl alcohol (a, 3.45 g, 10.9 mmol) in tetrahydrofuran (10 ml). Magnesium was then activated by the addition of dibromoethane (0.1 g). The metal went into solution slowly over a period of 8 hours. The Grignard reagent was then cooled to -78°C and treated with freshly distilled trimethyl borate (1.15 g, 11 mmol) added dropwise with stirring. The reaction mixture was then warmed to room temperature and stirred overnight. It was then treated with 2N hydrochloric acid till acidic and the tetrahydrofuran layer was separated from the aqueous layer. The aqueous portion was thoroughly extracted with ethyl acetate (5 x 50 ml) and the combined organic layer was washed with water and. finally with saturated sodium chloride. The organic phase was then dried, concentrated and chromatographed (flash silica gel). Elution with ethyl acetate/methanol (95:5) provided the boronic acid, which was recrystallized from ethyl acetate/ hexane. Yield: 0.69 g (38%), m.p. 218-220°C, M.S. 184 (M+NH4), 156, 140, JH NMR (DMSO-d6 ) : 2.7 (t, 2H), 4.6 (t, 2H), 7.1 and 7.7 (2d, 4H) and 7.9 (s, 2H) .

C. Preparation of 4- ( 2-bromoethyl )phenyl boronic acid To a solution of 4- ( 2-hydroxyethyl )phenyl boronic acid (1.66 g, 10 nunol) in dry dimethyl-formamide (25 ml), was added ethylene glycol (0.62 g, 10 nunol). The mixture was stirred under nitrogen at room temperature for 16 hours.

Dimethyl formamide was removed under reduced pressure and the resulting oil was kept under vacuum for 6 hours more. The oil was dissolved again in dry dimethylformamide (10 ml), cooled in an ice-bath, treated with triphenyl phosphine (5.25 g, 20 mmol) and N-bromosuccinimide (3.56 g, 20 mmol), and stirred under nitrogen for 6 hours at room temperature. Solvent was removed under reduced pressure and the residue was taken up in ether (100 ml). This was washed with water, dried and concentrated to give an oil which was chromatographed to furnish the bromo boronic acid as a colorless solid (flash silica gel, 1:1 ethyl acetate/Hexane ) . The product was recrystallized from dichloromethane/hexane . Yield: 1.4 g, m.p. 146-148°C.

D. Preparation of 4-(2-Nitroimidazolyl ethyl )- phenyl boronic acid 4-(2-Bromoethyl Jphenyl boronic acid (0.525 g, 2.72 mmol) and 2-nitroimidazole (0.3 g, 2.72 mmol) were heated in dry di ethylformamide (15 ml) in presence of anhydrous potassium carbonate (1.38 g, 10 mmol) under nitrogen with stirring at 60-70°C for 48 hours. Dimethyl formamide was removed under reduced pressure and the resulting gum was dissolved in a minimum amount of water and acidified with 2N hydrochloric acid. The precipitated solid was filtered off and washed with water. The combined aqueous portion was again extracted with ethyl acetate (5 x 50 ml). The organic layer was dried, concentrated and combined with the previously precipitated solid and then chromatographed (flash silica gel). Elution with 1:1 ethyl acetate/hexane yielded some unreacted starting bromide (0.1 g); continued elution with 2:1 ethyl acetate/hexane provided the required boronic acid as a pale yellow crystalline solid. The product was recrystallized from tetrahydrofuran/hexane . Yield: 0.25 g (36%), m.p. 229-231°C, M.S. (M+H)+ 262. 1E NMR (DMSO-d6): 3.1 (t, 2H), 4.65 (t, 2H), 7.11 (d, 2H), 7.14 (s, 1H), 7.5 (s, 1H), 7.69 (d, 2H) and 7.94 (s, 2H) .

Example 12 Preparation of 99mTc ( chlorine ) (1, 2-cyclohexane-dionedioxime ) 31- ( 2-nitroimidazoyl )benzylboron To a mixture of 10 mg citric acid, 100 mg of sodium chloride, 2 mg of 1 , 2-cyclohexanedione dioxime, 2 mg of diethylenetriamine-penta-acetic acid, 50 mg of gammacyclodextrin, 50 ug of stannous chloride, and 3 mg of 1- ( 2-nitroimidazoyl )benzyl boronic acid was added 1 mL of sodium pertechnetate (99mTc04"") in physiological saline.

The kit was heated at 100°C for 15 minutes. The yield of the title compound, as determined by high pressure liquid chromatography (HPLC), was 91.4%. Samples of this complex coeluted from Nucleosil HPLC columns at a retention time identical to that ooff aann aauutthheennttiicc Tc standard that was prepared as described below.

Example 13 99 Preparation of Tc( chlorine )( 1 , 2-cyclohexanedione-dioxime ) 31- ( 2-nitroimida2oyl ) benzyl boron 99 To 90.3 mg (0.11 mmol) of Tc( 1 , 2-cyclo-hexanedione dioxime )3 (u-OH)SnCl3 dissolved in 10 mL of warm acetonitrile was added 1- ( 2-nitroimida-zoyl )benzylboronic acid (31 mg, 0.125 mmol) and 1.5 mL of 3N hydrochloric acid. The solution was heated gently, with stirring. After 30 minutes, 10 mL of- 1 hydrochloric acid was added, and the solution was cooled to room temperature. The resulting orange precipitate (61 mg, 78% yield) was recrystallized from warm acetonitrile/lM hydrochloric acid.

Analysis calc'd for C28H34N9BCl08 c: C, 43.59; H, 4.43; N, 16.20; Found: C, 43.68; H, 4.45; N, 16.37.

A strong protonated molecular ion (M+H)+ was observed at m/z = 770. Samples of this complex eluted from Nucleosil HPLC columns at a retention time of 2.34 minutes (80/20 ACN/0.1 M citric acid, 1.5 mL/minutes).

Example 14 Preparation of "^(chlorine) (dimethylglyoxime )3-1- ( 2-nitroimida2oyl )benzylboron To a freeze-dried mixture of 2 mg of dimethylglyoxime, 18 mg citric acid, 100 mg of sodium chloride, 1 mg of diethylenetriamine-penta-acetic acid, 50 mg of gammacyclodextrin, 50 ug of stannous chloride, and 3 mg of 1- ( 2-nitroimidazoyl ) -benzyl boronic acid was added 1 mL of sodium 99m — pertechnetate ( Tc04 ) in physiological saline.

The kit was heated at 100°C for 15 minutes. The yield of the title compound, as determined by high pressure liquid chromatography (HPLC), was 73.4%.

Samples of this complex eluted from Nucleosil HPLC columns at a retention time identical to that of 99 an authentic Tc standard that was prepared as described below.

Example 15 99 Preparation of Tc ( chlorine )( dimethylglyoxime )3-1- ( 2-nitroimidazoyl )benzylboron 99 To 55 mg of Tc ( dimethylglyoxime ) 3 (u-OH)-SnCl3 (0.074 mmol) was added 25 mg (0.10 mmol) of l-( 2-nitroimidazoyl )benzylboronic acid, dissolved in 10 mL of acetonitrile. One mL of 3N hydrochloric acid was added, and the solution was heated gently for 30 minutes. Ten mL of 1M hydrochloric acid was added, and the solution was cooled to room temperature. The resultant orange crystals (32 mg, 62.3% yield) were recrystallized from a warm acetonitrile/lM hydrochloric acid solution to give analytically pure complex, isolated as the 0.5 H20 hydrate.

Analysis calc'd for 5Tc: C, 37.62; H, 4.33; N, 17.63; Found: C, 37.71; H, 4.17; N, 17.99.

Samples of this complex eluted from Nucleosil HPLC columns at a retention time of 3.45 minutes (60/40 ACN/0.1 M citric acid, 1.5 mL/minutes ) .

Example 16 9Qro Preparation of Tc ( chlorine )( dimethylglyoxime ) 3 -4- ( 2-nitroimidazolylethyl )phenyl Boron To a mixture of 18 mg citric acid, 100 mg of sodium chloride, 2 mg of dimethylglyoxime, 1 mg of diethylenetriamine-penta-acetic acid, 50 mg of gammacyclodextrin, 50 pg of stannous chloride and 3 mg of 4-(2-nitroimidazolyl ethyl )phenyl boronic acid was added 20 mCi of 99mTc0 ~ in 1 ml of physiological saline. The kit was heated at 100°C for 15 minutes to give 93% yield of the title complex, as determined by HPLC.

Example 17 Compounds containing nitro-heterocyclic groups are retained in hypoxic tissue by reduction of the nitro-moiety in such groups. Therefore, redox potential for nitro-heterocyclic groups is considered to be an indicator of the degree to which such groups can be retained by hypoxic tissue .

Cyclic voltammetry studies in DMF solvents were performed using a standard 3-electrode configuration (Heinze, J. Ang. Chem. Int., Ed. Eng., 23, 831, 1984). Data were obtained using a PAR 174A polarographic analyzer interfaced with PAR 303 static mercury drop electrode apparatus and recorded on a PAR RE0074 X-Y recorder. The reference electrode was Ag/AgN03 in acetonitrile ; the working electrode was mercury.

Sample solutions, typically 0.3-1.2 mM, contained 0.1 tetrabutyl mmonium tetrafluoroborate supporting electrolyte, and were degassed with solvent-saturated N2 before measurements .

Table 2 Electrochemistry Results from DMF Peak Potential (EP) Values-(scan rate=100 mV/sec) 1Έ>ΑΊΟ is boronic acid technetium oxime and refers to the boronic trioxime complexes of technetium. 2Technetium( chloride) (dimethylglyoxime) 3 (methyl boron) .

Example 18 Previous in vitro and in vivo studies with nitroimidazole containing compounds have demonstrated that a probable mechanism for intracellular binding of nitroimidazoles results from enzymatic reduction of the nitro group to a chemically reactive species (for example, Clarke, Wardman, and Goulding, Biochem. Pharmacol. (1980) 29, 2684 - 2687). The nitroimizole boronic acids in this invention were examined in an assay using the enzyme xanthine oxidase. Assay solutions contained the following Hypoxanthine 1 ml of 0.01M solution moles of substrate xanthine oxidase 0.5 Units of 500 μΐ of pH 7.4 Na phosphate Na phosphate buffer 1.0 ml, 0.1 , pH 7.4, mg/L Na2EDTA Nitro compound 0.25 Moles in 20 μΐ of dimethylformamide Reactions were initiated by adding enzyme to a solution of all other reagents in a septum-sealed cuvette. All reagents were degassed prior to mixing by passage of argon over the surface for minutes. Loss of the nitro group (an indication of reduction) was monitored every 5 minutes using a UV/Visible spectrophotometer set at 326nm. The half-lives of disappearance of the nitro compounds were determined by plotting log (concentration) mmole/ml vs time for all compounds studied. The results are shown in table 2, with data on two the two reference compounds, misonidazole and metronidazole shown for comparison.

Table 2 COMPOUND half life Epc (DMT)■·'■" Epc (Aqueous ) (enzyme assay) Metronidazole >24 hr •1.62 V -0.46 V (0H)2BB4N02 95 min. ■1.80 V -0.50 V Misonidazole 45 min. ■1.49 V -0.33 V (0H)2BPhEtN02 42.5 min ■1.53 V -0.30 V (0H)2BPropeneN02 24 min. ■1.56 V -0.30 V (0H)2BBN02 11 min. ■1.52 V -0.32 V Example 19 Preparation of 2-Nitroimidazolyl-N^- [2-propenyl ] -3- boronic acid ( BpropenNO., ) 2-Nitroimidazole (1.0 g, 8.84 mmol) in dry dimethyl formamide (15 ml) was treated with anhydrous potassium carbonate (6.9 g, 50 mmol) and stirred for 0.5 hr. at room temperature under nitrogen. The solution was cooled to 0°C and then treated with 2-bromoethyl-2-ethenyl-l , 3 , 2-benzo-dioxoborole (4.23 g, 17.7 mmol) in dry tetrahydro-furan (10 ml) over a period of 1 hour with stirring under nitrogen at 0°C. The reaction mixture was then heated at 60 - 70°C for 48 hours with stirring under nitrogen, dimethyl formamide was removed under reduced pressure and the residue was dissolved in methanol (100 ml). The solution was acidified with Dowex 50X8 resin (H+) and filtered. The resin was washed with methanol and the combined filtrate and wash was concentrated and chromatographed to yield a semi solid (silica gel, 230 - 400 mesh, 2% methanol in EtOAc) which was recrystallized from dichloromethane to give a pale yellow crystalline solid. Yield: 0.3 g, m.p. 138 - 140°C.

½NMR (D SO-d6): δ 5.2 (d, 2H), 6.6 (m, 1H), 7.15 (s, 1H), 7.4 (s, 1H) and 7.7 (s, 2H) Analysis: Calculated for C6HgB 304, C 36.59, H 4.09, N 21.34, Found C 36.79, H 3.66, N 21.41.

Example 20 Preparation of 2-Nitroimidazolyl-N1-propyl-3-boronic acid (BpropNO^) A mixture of hydroxylamine hydrochloride (0.417 g, 6 m ol ) , sodium acetate (0.492g, 6 mmol), ethylacetate (0.176 g, 2 mmol) and BpropenN02 (Example 19, 0.2 g, 1 mmol) in ethanol (25 ml) was refluxed with stirring under argon for 30 hours. After cooling, the solvent was removed, and the crude product was directly loaded on to a flash silica gel column and chromatographed. The isolated product was rechromatographed twice more to yield the product as a pale yellow solid.

Yield: 0.02 to 0.025 g (20 - 25%) m.p. 122 -124°C.

½ NMR (DMSO-d6): 6 0.8 (t, 2H, B-CH2 ) , 1.9 (m, 2H), 4.4 (t, 2H, N-CH2), 7.2 (s, 1H), 7.8 (s, 2H, B-OH) and 7.85 (s, 1H) M.S. (M + H)+ - 200, 172, 154 and 109. Analysis: Calculated for C6H1QN3B04:: C 36.22, H 5.02, N 21.11 Found: C 36.87, H 4.84, N 21.56.

Example 21 Preparation of 1- ( 4-Nitroimidazole ) -benzylboronic acid ( BB4NQ2 ) This compound was prepared by reaction of 4-nitroimidazole (1.13 g, lOmmol) and 4-bromo-methylphenyl boric acid (3.25 g, 15 mmol), by the method described in Example 10. Yield: 1.7 g m.p. 163 - 165°C.

½ NMR [DMSO-d,]: δ 5.4 (s, 2H), 7.4 (d, 2H), 7.9 13 (d, 2H), 8.2 (bs, 2H) and 8.6 (s, 1H). JC NMR [DMSO-d6]: δ 50.76, 121.59, 126.86, 134.54, 134.66, 137.45, 137.89 and 147.18. Analysis: Calculated for C10H1QBN3O4 C 48.62, H 4.08 N 17.01. Found C 49.39, H 4.21, N 16.83. M.S.

[M+Gly-2 H20 + H]+ 304.

Example 22 Preparation of "TCCI ( DMG ) 3BPhEtN02 To Tc(DMG)3(M-OHSnCl3.3H20 (77.1 mg, 0.104 mmol ) in 5 ml of acetonitrile was added (OH)2BPhEtN02 (Example 11, 28.8 mg, 0.11 mmol), followed by 2 drops of cone. HCl. The solution was heated at a boil for 30 minutes during which time an orange solid precipirated (68 mg, 93% yield). 'The precipitate was isolated by filtration and was washed well with acetonitrile and dried in vacuo. This solid was dissolved in 1 ml of dimethylformamide, 2 ml of acetonitrile and 1 ml of 1M hydrochloric acid and the solution was boiled for 30 minutes. Crystals of the product (31 mg, 40% overall yield) formed upon cooling overnight. Anal. Calcd for TcCl(DMG)3BPhEtN02. 0.5DMF, C24 5H33Ng 5BC10Q 5Tc. Found: C, 39.80, H, 4.60; N, 17.55. Calcd: C, 39.64; H, 4.81; N, 17.92 Example 23 Preparation of 99m, [Tc ( chlorine ) ( dimethylqlyoxime )-,-!-( n-propyl- 2-nitroimidazolyl )boron The title compound was prepared as described in Example 14, except that 4 mg of BpropN02 (example 20) was substituted for the l-(2-nitro-imidazolyl )-benzyl boronic acid. The yield of title complex, as determined by high pressure liquid chromatography (HPLC), was 52%. Samples of this complex eluted from a Nucleosil HPLC, was 52%. Samples of this complex eluted from a Nucle-sil HPLC column with a retention time identical to 99 that of an authentic Tc standard that was prepared as described in Example 24.

Example 24 Preparation of 99 Tc ( chlorine ) ( dimethylglyoxime )-,-!- ' (n-propyl-2-nitroimidazolyl ) boron To Tc(DMG)3(M-OH)SnCl3-3H20 in 10 ml of acetonitrile was added (OH)2BPropN02 (example 20, 41.8 mg, 0.21 mmol), followed by 3 ml of 2N HC1. The reaction mixture was heated gently for 30 minutes', 50 ml of IN hydrochlorice acid was added, and the solution was cooled to room temperature. The resultant flocculant orange solid was isolated by suction filtration, washed with 1M hydrochloric acid and H20 and dried in vacuo to yield 97 mg (78%) crude product. This was dissolved in 1 ml of CHCl^ and chromatographed on a 1 x 10 cm silica gel column that was conditioned and eluted with CHCl-j . The major orange band was evaporated to dryness, redissolved in 3 ml of CH2C12 and treated with 30 ml of hexane. Analytically pure solid was isolated in 57% yield overall. Anal. Calc for C18H28 9BC10gTc. Found: C, 33.66; H, 4.20; N, 19.28. Calc: C, 33.58; H, 4.38; N, 19.58.

Example 25 Preparation of 99mTc( chlorine ) ( dimethylglyoxime )..- 1- (propene-2-nitroimidazolyl )boron (KL L498-178) The title compound was prepared as described in Example 14, except that 3 mg of BpropenN02 (Example Ί9 ) was substituted for the l-(2-nitro-imidazolyl )-benzyl boronic acid. The yield of title complex, as determined by high pressure liquid chromatography (HPLC), was 58%.

Example 26 Preparation of 99mTC ( chlorine ) ( dimethylqlyoxime ) 3-I- (4-nitroimidazolyl )benzylboron The title compound was prepared as described in Example 14, except that 3 mg of BB4N02 (Example 21) was substituted for the 1- ( 2-nitroimidazolyl ) -benzyl boronic acid. The yield of the title complex, as determined by high pressure liquid chromatography (HPLC), was 82%. Samples of this complex eluted from a PRP-1 HPLC column with a retention time identical to that of any authentic 99 Tc standard, prepared as described m Example 27.

Example 27 Preparation of 99 · .

Tc(chlorine ) ( dimethylglyoxime )^-l- (4-nitroimidazolyl )benzylboron A mixture of TcCl (DMG)3 (32.7 mg, 0.068 mmol) and BB4N02 (example 21, 17.7 mg, 0.073 mmol) in 5 ml of acetonitrile and 0.5 ml of 2N HC1 was heated with stirring for 15 minutes. Solvents were then removed by evaporation. The product was purified on a silica gel column eluted with 40/60 ACN/CH-Cl,. The major orange band was evaporated to dryness and recrystallized from ether (61% yield). Anal. Calcd for TcCl (DMG )3BB 02.0.2 C4H1Q0 (C22HgNgOaBCITc.0.2C4H10O. Found: C, 38.39; H, 4.21; N, 17.44. Calcd: C, 38.75; H, 4.28; , 17.84. FAB-MS(+): m/z 692, [ +H] ; 656, [M-Cl; 579, [M-4-nitroimidazole] . 1H NMR (270 MHz, CDC13): δ 2.9 (m, 12H, CDO), 3.0 (m, 12 H, COO), 5.2 (s, 2H, Bz), 7.2 (d, 2H, Ph), 7.4 (s, 1H, imidazole), 7.7 (s, 1H, imidazole), 7.8 (d, 2H, Ph), 14.8 (s, 2H, oxime ) . IR (KBr) (cm-1): 3505 br, 1634, 1545, 1491, 1399, 1338, 1228, 1206 s, 1089 s, 990 s, 928, 909, 824, 808. UV-VIS (CH3CN) :Amax(Loge ) 288(4.08), 382(3.80), 460(3.41) Example 28 Preparation of 99m Tc( chlorine ) ( 1 , 2-cyclohexane-dionedioxime )^- 1- (4-nitroimidazolyl )benzylboron The title compound was prepared as described in Example 12, except that 3 mg of BBNC^ (Example 21) was substituted for the 1- ( 2-nitroimidazolyl )-benzyl boronic acid. The yield of title complex, as determined by high pressure liquid chromato-graphy (HPLC), was 86%. Samples of this complex eluted from PRP-1 HPLC columns at a retention time 99 identical to that of an authentic Tc standard that was prepared as described below.

Example 29 Preparation of 99m Tc(chlorine ) ( 1 , 2-cyclohexane-dionedioxime ) ., - 1- ( 4-nitroimidazolyl )benzylboron A mixture of TcCl(CDO)3 (25.7 mg, 0.046 mmol) and BB4N0,, (Example 21, 11.6 mg, 0.48 nvmol ) was dissolved in 5 ml of ACN and 0.5 ml of 3M hydrochloric acid and heated with stirring for 30 minutes. Orange solid was precipitated by adding 5 ml of 1M hydrochloric acid and collected by filtration (crude yield, 83%).

Anal. Calcd. for . 0.5 C4H1Q0: C, 44.65; H, 4.87; N, 15.62. Found: C, 44.81; H, 4.95; N, 16.05. FAB-MS (+) : m/z 769, M; 734, [M-Cl]; 657, [M-4-nitroimidazole] . ½ NMR (270 MHz , CDC13): δ 2.4 (m, 18H, Me), 5.2 (s, 2H, Bz ) , 7.2 (d, 2H, Ph), 7.5 (s, 1H, imidazole), 7.7 (s, 1H, imidazole), 7.8 (d, 2H, Ph), 14.8 (s, 2H, oxime). IR (KBr) (cm"1): 3450 br, 1631, 1546, 1446, 1430, 1380, 1337, 1286, 1229, 1203 s, 1061 s, 960 s, 924, 902, 866, 847. UV-VIS (CH3CN) :\max(Log ε) 290(4.35), 386(4.11), 462(3.76) Example 30 Preparation of 99mTc ( hydroxy ) ( dimethylglyoxime )3 )- 1- ( 2-nitroimidazolyl )benzylboron The compound "^Tc ( chlorine )( dimethylglyoxime )3-l-( 2-nitroimidazolyl )benzylboron was prepared as described in Example 14. It was then purified by adsorption onto PRP-1 reverse phase resin. The resin was washed with 1 ml of saline and 1 ml of 1:1 ethanol/saline , and then the complex was eluted with 0.4 ml of 95% ethanol. A 400 μΐ aliquot of pH 8.0 phosphate buffer (0.1M) was added and the mixture was heated at 37 °C for minutes. During this time, theaxial chloro ligand was replaced by a hydroxyl group in 96% yield as determined by HPLC. Sample of this complex coeluted with authrntic samples of 99 Tc( OH(dimethyl glyoxime ) _-l- ( 2-nitroimidaoyl ) - 99 benzyl boron, prepared by treatment of the Tc-chloro complex with aqueous sodium hydroxide.

Example 31 Preparation of Tc( chlorine ) ( 1 , 2-cyclohexane- dionedioxime )^-l- (propane-nitroimidazolyl )boron The title compound was prepared as described in Example 12, except that 3 mg of BpropNC^ (Example 20) was substituted for the l-(2-nitroimi-dazolyl ) -benzyl boronic acid. The yield of title complex, as determined by high pressure liquid chromatography (HPLC), was 95%.

Example 32 Preparation of 99m, Tc(chlorine ) ( 1 , 2-cyclohexane-dione- dioxime )^-l- (propene-nitroimidazolyl )boron The title compound was prepared as described in Example 12, except that 3 mg of BpropenNC^ (Example 19) was substituted for the l-(2-nitro-imidazolyl ) -benzyl boronic acid. The yield of title complex, as determined by high pressure liquid chromatography (HPLC), was 83%.

Example 33 Preparation of (R)-l-Azabicyclo [2 , 2 , 2 ]oct-3-yl-(R)-a- (4 ) -Phenylboronic acid-a-phenylacetate ( R , R-QNB boronic acid) This compound was prepared by the following reaction scheme: A. (RS )-3-Acetoxyquinucldine A solution of (RS )-3-quinuclidinol (25 g, 0.2 mmol) in pyridine (100 ml) was treated with acetic anhydride (100 ml), kept at 50°C for 4 hours and left at room temperature for 15 hours After removal of the pyridine and excess acetic anhydride under vacuum, the clear light brown o was then dissolved in water (25 ml) and made slightly alkaline with saturated potassium carbonate. The ester was then extracted with chloroform (5 x 50 ml) and extracts were dried over K2C03. After evaporation of the solvent in vacuo the residue was distilled yielding 20.6 g (62%) of ( RS )-3-acetoxyquinuclidine as a colorless liquid. 1HNMR (CDC13) δ 1.31 - 2.01 (m, 6H), 2.11 (s, 3H, OCOCH3), 2.62 - 2.95 (m, 5H), 3.18 - 3.31 (m, 1H), 4.80 (m, 1H, 3H).

B. (R)-(+ )-3-Acetoxyquinuclidine ( RS ) -3-Acetoxyquinuclidine (34 g, 0.2 mmol ) was added to a solution of L- ( + )-tartaric acid (30.13 g, 0.2 mmol) dissolved in ethanol (80%, 142 ml). The solution was kept overnight at room temperature. The colorless crystalline solid (40 g) filtered and recrystallized twice from ethanol (80%), 280 ml) providing 25.5 g (65%) of resolved* tartrate salt of (R)-(+)-3-acetoxyqui-nuclidine mp 96 - 98°C. Lit. 2 mp 94 - 95.5°C. The resolved tartrate salt of (R)-(+) —3-acetoxy-quinuclidine (25.0 g) was dissolved in water (5 ml) and the solution made faintly alkaline with saturated K2C03, and extracted with chloroform (5 x 25 ml). The combined CHC1- extracts were dried over anhydrous Na2S04 and filtered. After evaporation of the solvent in vacuo the residue was distilled to provide ( R ) - ( + ) -3-acetoxyquinucli-dine as a colorless liquid. Yield: 10.7 g (88%) [a]D25+29.96° (c 2.93, ethanol ) . Lit. (Cohen et al. J. Pharm. Sci., (1989), 78, 833 - 836 (c 3.0, ethanol). ) δ 1.30 - 2.01 (m, 6H), 2.13 (s, 3H, OCOCH3), 2.62 - 2.98 (m, 5H), 3.18 - 3.30 (m, 1H), 4.82 (m, 1H, 3-H).

C. (R)-(+)-4-Nitrobenzilic acid To a suspension of quinidine (39.6 g, 90%, 1.1 mmol) in boiling ethyl acetate (250 ml) was added the racemic (RS ) -4-nitrobenzilic acid (30.0 g, 1.1 mmol) and kept at room temperature for 18 hours. The salt which crystallized was filtered, and after four crystallization from ethyl acetate had a constant melting point of 120 - 122°C; Yield 19.5 g (59.4%) TLC [silica gel, toluene-HOAc 9:1] Rf 0.24.' The quinidine salt (lg, 1.68 mmol) was then treated with an excess of 6M hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous MgS04 and the solvent was removed under reduced pressure to afford a past which was then loaded onto a silica gel (8 g) column and eluted with CH2Cl2- eOH (95:5). The fractions with compound were pooled together and evaporated to a colorless paste which crystallized slowly to a cream colored solid. Yield: 0.35 (77%) mp 104 - 106 C thin layer chromatography [silica gel, toluene-HOAc 9:l]Rf 0.3; [o]D25 + 50.11° (c 1.34, acetone). Lit. ( Rzeszotarski et al. J. Med. Chem., (1981), 27, 156 - 160). [a]D24 + 49.4° (c 1.34, acetone).

½ NMR (CDCl3) 64.80(bs, 2H, COOH and OH, 7.35 (m, 5H, C6H5), 7.71 and 8.21 (2d, 4H, 6H4).

D. (R)-4-Aminobenzilic acid A solution of (R)-4-nitrobenzilic acid (2.0 g, 7.33 mmol) in ethanol (25 ml) was treated with hydrazine (1.0 ml) and Raney-Ni (0.8 g) and stirred at room temperature for 18 hours unders nitrogen atmosphere. The Raney-Ni powder was removed by filtration, washed with ethanol, the ethanol layer concentrated to a small volume and diluted with water (75 ml). The aqueous layer was extracted with ether (2 x 50 ml) and the aqueous layer was evaporated under vacuum to provide a light yellow solid of (R)-4-aminobenzilic acid in 82% yield (1.4.6 g); mp 139 - 140°C (decomp); TLC [silica gel, acetone]Rf 0.20; ½ NMR (D20) δ 6.75 and 7.18 (2d, 4H, &H4) and 7.31 (s, 5H, C&H5 ) .

(R)-4-Iodobenzilic acid The iodobenzilic acid was prepared by adding se over 30 minutes a solution of soidum nitrite (1.7 g, 24.64 mmol) in water (10 ml) to a solution of (R)-4-aminobenzilic acid (3.0 g, 12.35 mmol) in 10% hydrochloric acid (100 ml) at -5°C. Stirring was continued for an additional 30 minutes at -5°C, then a solution of potassium iodide (4.09 g, 24.64 mmol) in water (10 ml) was added slowly. The reaction mixture was then stirred at 0°C for 1. hour, then at ambient temperature for 1 hour. The resultant mixture was extracted with exthyl acetate (3 x 75 ml), and the combined extracts were washed with aqueous sodium thiosulfate (10%, 2 x 50 ml), water (2 x 50 ml) and dried over sodium sulfate. Removal of solvent afforded a brown past, which was purified by column chromatography (silica gel, eluted with ethanol/dichloromethant) to give the product as a light yellow solid. Yield 2.18 g (50%); mp 80 -81°C; TLC [silica gel, toluene-acetic acid 9:1] Rf 0.40; [a]D25 + 24.7° (c 0.132, acetone); ½ NMR (CDC13) δ 5.50 (bs, 2H, COOH and OH), 7.21 and 7.69 (2d; 4H, CgH4) and 7.41 (s, 5H, CgH-j ) .

F . ( R ) -3-Quinuclidinyl- ( R ) -4-iodobenzilate A solution of (R)-4-iodobenzilic acid (0.26 g, 0.74 mmol) in dry dimethyl formamide (2 ml) was treated with 1 , 1 ' -carbonyldiimidazole (0.12 g, 0.74 mmol) in small portions and stirred at room temperature for 1 hour under nitrogen atmosphere.

To this light yellow colored solution, was added (R)-3-quinuclidinol (0.93 g, 0.73 mmol) and stirring was continued for an additional 15 hours at room temperature. The reaction mixture was concentrated under vacuum and added to water (50 ml) and extracted with ether (3 x 30 ml). The combined ether extracts were washed with saturated sodium bicarbonate (2 x 20 ml), water (2 x 20 ml) and dried over anhydrous sodium sulfate. To the paste thus obtained, added silica gel (0.5 g), ether (5 ml) and dried. The dry silica gel powder with compound was loaded onto a silica gel column (10 g) and eluted with 5% methanol in dichloro-methane solvent mixture. The fractions with compound were pooled together and evaporated on a rotary evaporator to afford a light yellow solid in 75% yield (0.256 g); mp 124 - 127°C; TLC[silica gel, MeOH- H4OH 98:2] Rf 0.65; ½ NMR (CDC13) δ 1.15 - 1.89 (m, 4H), 2.01 (s, 1H) 2.42 - 2.81 (m, 5H), 3.21 (m, 1H), 4.52 (bs, 1H, OH), 5.01 (m, 1H), 5.01 (m, 1H) and 7.15 - 7.82 (m, 9H, Ar-H).

G. (RR)-QNB boronic acid To a solution of (R)-3-quinuclidinyl-(R)-4-iodobenzilate (0.60 g, 1.3 mmol ) in freshly distilled tetrahydrofuran (2.0 ml) in dry 10 ml RB flask at -78°C was added via syringe n-BuLi (0.2 g, 2.5 M, 1.25 ml, 3.13 mmol) slowly and stirred at the same temperature for 20 minutes. Then a freshly distilled triethyl borate (0.378 g, 0.441 ml, 2.59 m ol ) was added to this reaction mixture and stirred for an additional 1 hour at -78°C, allowed to raise its temperature to ambient condition, and stirred for 18 hours. The reaction mixture was then treated with few drops of water, decanted to remove solution phase from the semisolid which was then repeatedly washed with ether and finally triturated with ether to a colorless solid. The solid was then dissolved in water containing <5% acetonitrile, filtered and loaded onto a reverse phase C^g HPLC column (Dynamax C^g, 4.14 x 25 cm, 8 micron) and eluted under isocratic condition with 12.5% acetonitrile containing 0.1% trifluoroacetic acid/H20. The fractions were checked via analytical HPLC (Dynamax 0.46 x cm, 8 micron, 18% acetonitrile with 0.1% tri-fluoroacetic acid in 0.1% trifluoroacetic acid/-water) and the fractions with the title compound in >98% purity were pooled, and freeze-dried to afford (RR)-QNB boronic acid as a colorless solid in trifluoroacetic acid salt form; yield: 0.025 g (4.4%); ½ NMR (CD3OD) δ 1.68 (m, 2H), 1.95 (m, 2H), 2.35 (s, 1H), 2.81 - 3.35 (m, 5H), 3.80 (m, 1H), 5.31 (m, 1H) and 7.28 - 7.71 (m, 9H, Ar-H). MS: Exact Mass calculated for 438.2092; experimental, 438.2088.

Example 34 Preparation of (S)-l-Azabicyclo [2,2,2 Toct-3-yl-(R)-a- Hydroxy-a - ( 4 ) -Phenylboronic acid-a - phenylacetate (R, S-QNB boronic acid) This compound was prepared by the reaction scheme outline in Example 33, substituting S-quinuclidinol for R-quinuclidinol .

A. ( S ) -3-acetoxyquinuclidine The mother liquors from Example 33A (preparation of (R)-3-acetoxyquinuclidine ) , were concentrated in vacuo and the residue was made alkaline with potassium carbonate. The ester was extracted with chloroform (3 x 50 ml) and dried with sodium sulfate. The solvent was evaporated yielding 7.5g of the crude ester. The ester was added to a solution of (-)-tartaric acid 6.5 g in 80% ethanol and the salt formed was purified as described in Example 33A. mp. 95 - 96°C. lit(Cohen et al . J. Pharm. Sci., (1989), 78, 833 -836) mp 94 - 96°C.

B . ( S ) -3-Quinuclidinyl- ( R ) -4-iodobenzilate The title compound was prepared as a colorless past in 73% yield (0.25 g) from (R)-4-iodobenzilic acid (0.26 g, 0.73 mmol), 1,1'- carbonyldiimidazole (0.12 g, 0.74 mmol) and (R)-3-quinuclidinol (0.93 g, 0.73 mmol) in dry dimethyl (2 ml) as described for the synthesis of (R)-3-quinuclidinyl-(R)-4-iodobenzilate (Example 33); TLC [silica gel, MeOH-NH^OH 98:2]Rf 0.69; 1H NMR (CDC13) δ 1.15 - 1.89 (m, 4H), 2.01 (s, 1H), 2.42 - 2.81 (m, 5H), 3.21 (m, 1H), 4.52 (bs, 1H, OH), 5.01 (m, 1H), 5.01 (m, 1H) and 7.15 - 7.82 (m, 9H, Ar-H) .

C. (S)-l-Azabicyclo[2, 2 , 2 ] oct-3-yl- ( R ) -a - Hydroxy-a- (4 )-Phenylboronic acid-a- phenylacetate The above mentioned compound was synthesized as a colorless solid (TFA salt form) in 11% yield (58 mg) from ( S ) -3-quinuclidinyl- ( R ) -4-iodobenzi-late (0.6 g, 1.3 mmol), n-BuLi (0.2 g, 2.5 M, 1.25 ml, 3.13 mmol) and triethyl borate (0.378 g, 0.441 ml, 2.59 mmol) in dry tetrahydrofuran at -78°C as described for the synthesis of (RR)-QNB boronic acid (Example 33); ½ NMR (CD3OD) δ 1.68(m, 2H), 1.95(m, 2H), 2.35(s, 1H), 2.81 - 3.35(m, 5H), 3.80 (m, 1H), 5.31(m, 1H)) and 7.28 - 7.71 (m, 9H, Ar-H). MS: Exact Mass calculated for C24H2g06NB: 438.2092; experimental, 438.1190.

Example 35 Preparation of ( S )-l-Azabicyclo [2,2,21oct-3-yl- ( S )-α· Hydroxy-g - ( 4 ) -Phenylboronic acid-a- phenylacetate (S,S-QNB boronic acid) This compound was prepared by the following reaction scheme: A. (RS )-4-Bromobenzilic acid To a solution of 4-bromobenzophenone (54.81 g, 0.21 mol ) in dry dichloromethane (500 ml) was added zinc iodide (0.5 g) and stirred at room temperature under N2 atmosphere. Then trimethylsilyl cyanide (25 g, 0.25 mol) was added in drops from an addition flask over a period of 1 hour and stirred at room temperature for 72 hours. The reaction mixture was then treated with saturated sodiumbicarbonate (200 ml) and stirred for 1 hour. The organic layer was separated, washed with water (2 x 150 ml) and concentrated. The residue was suspended in H20:HCl:AcOH (1:3L3; 500 ml) and heated at 85 - 90°C via an oil-bath for 48 hours. The solution was then concentrated under vacuum to about 100 ml and treated with saturated sodiumbicarbonate (400 ml) and extracted with ether (3 x 100 ml). The aqueous layer was then acidified with 6N hydrochloric acid and the separated solid was dissolved in ether (300 ml).

This organic layer was washed with water, filtered and the filtrate was evaporated to provide a colorless crystalline solid of (RS )-4-bromobenzilic acid in 19% yield (12 g); mp 125 - 126°C; TLC[silica gel, toluene-acetic acid] Rf 0.32; ½ NMR (DMSO-d6) 6 2.38 (bs, 2H, COOH and OH) and 7.38 - 7.70 (m, 9H, AR-H).

B. 3-S-Quinuclidinyl 4 ' -bromobenzilate Ν,Ν'-Carbonyldiimidazole (0.810 g, 0.005 mol ) was added to solution of racemic p-bromo-benzilic acid (1.53 g, 0.005 mol) in dimethyl-formamide (5 ml) under nitrogen atmosphere and the mixture was stirred for 1 hour at 40°C. S-Qui-nuclidinol (0.8 g, 0.0063 mol) was added and the mixture was stirred at 40°C for 24 hours. Workup afforded 1.12 g of 3-S-quinuclidinyl 4'-bromo-benzilate. mp . 151-53°C. ½ NMR (DMSO-d6) δ 1.3 - 3.3 (m, Quinuclidinylprotons ) , 4.9 (m, 1H,CH0), 7.3 - 7.7 ( m , 9H, ArH ) . MS: (M2 + H)+ = 416+ and 418+'.

C. (S)-l-Azabicyclo[2,2,2]oct-3-yl-(S)-cf- Hydroxy-a- ( 4 ) -Phenylboronic acid-a - phenylacetate To a cooled (-78°C) solution of 3-S-quinuclidinyl 4 ' -bromobenzilate (417 mg, 0.001 mol) in dry tetrahydrofuran (30 ml) was added n-BuLi (2.5 M solution in hexane, 1.0 ml, 0.165 g, 0.0025 mol) via a syringe. The mixture was stirred for 1 hour at -78 °C and triethylborate (2 ml) was added at -78°C. The mixture was stirred for an additional 1 hour at -78°C and 4 hours at room temperature. Tetrahydrofuran was removed and the residue was treated with water and extracted with ethyl acetate and dried with sodium sulfate.

The solvent was evaporated to yield a semisolid which was triturated with ether to give 100 mg of (RS ) , S-QNB-boronic acid, mp 212 - 215°C (decomp). The S,S stereoisomer was isolated from this mixture of diastereoisomers by preparative HPLC, as described in Example 33G. ½ NMR of the S , S-stereoisomer (D20): δ 1.40 -1.70 (m, 2H), 1.17 -3.03 (m, 2H), 2.32 (s, 1H), 2.65 - 2.85 (m, 1H ) , 3.)) - 3.22 (m, 4H), 3.60 (m. 1H ) , 5.28 (m, 1H), 7.35 (m, 7H), 7.72 (d, 2H).

Example 36 Preparation of (R)-l-Azabicyclo[2, 2 , 21 oct-3-yl- ( S ) -a - ( 4 ) -Phenylboronic acid-a -phenyl acetate ( S , R-QNB boronic acid) This compound was prepared by the reaction scheme shown in Example 35.

A. 3-R-Quinuclidinyl 4 ' -bromobenzilate Ν,Ν' -Carbonyldiimidazole (0.810g, 0.005 mmol ) was added to a solution of p-bromobenzilic acid (Example 35A, 1.53 g, 0.005 mmol) in dimethyl-formamide (5 ml) under nitrogen and the mixture was stirred for 1 hour at 40°C. R-Quinuclidinol (0.8 g, 0.0063 mol ) was added and the mixture was stirred at 40°C for 24 hours. Dimethyl formamide was removed under vacuum and the residue was poured into water. The precipitated solid was filtered and air dried. Yield 1.2 g (58%). ½ NMR (DMSO-d6) δ 1.3 - 3.3 (m, Quinuclidinyl protons), 4.9 (m, 1H, CHO ) , 7.3 - 7.7 (m, 9H, ArH ) . MS M2 - H)+ = 416+ and 418+.

B. (R)-l-Azabicyclo[2, 2 , 2 ] oct-3-yl- ( S ) -a- Hydroxy-o-(4 ) -Phenylboronic acid-cr- phenylacetate To a cooled (-78°C) solution of 3-quinucli-dinyl 4 ' -bromobenzilate (316 mg, 0.00076 mol) in dry tetrahydrofuran (30 ml) was added n-BuLi (2.5 M solution in hexane, 0.72 ml, 0.12, 0.0018 mol) via a syringe. The mixture was stirred for 1 hour at -78°C and triethylborate ( 1 ml ) was added at -78 °C. The mixture was stirred for an additional 1 hour at -78°C and 4 hours at room temperature. Tetrahydrofuran was removed and the residue was treated with water and extracted with ethyl acetate and dried with sodium sulfate. The solvent was evaporated to yield a semisolid which was triturated with ether to give a solid. Yield 50 mg. The S,R stereoisomer was isolated from this mixture of diastereoisomers by preparative HPLC, as described in Example 33G. mp 213 - 215°C (decomp). ½ NMR (D20) δ 1.41 - 1.70 (m, 2H), 1.71 - 2.02 (m, 2H), 2.32 (s, 1H), 2.65 - 2.85 (m, 1H), 3.00 - 3.22 (m, 4H)( 3.60 ( , 1H), 5.28 (m, 1H), 7.35 (m, 7H), 7.72 (d, 2H).

Example 37 Preparation of [TcCl(DMG)3 [ (RR or RS)QNB boron] Into a 5 ml siliconized serum vial were measured 2.0 mg of dimethyl glyoxime, 1.5 mg of 3-R-quinuclidinyl- ( 4-borono-Rbenzilate ) ( RR-QNB-boronic acid) or 3-R-guinuclidinyl- ( 4-borono-S-benzilate ) ( RS-QNB-boronic acid), 20 mg of citric acid, 100 mg of NaCl, 2.0 mg of diethylenetriaminepenta-acetic acid, and 125 g of SnC^ (in 4 M HC1) in a total volume 0.7 ml of 28% 99m ethanol/saline . 0.5 ml of TcO^-generator eluent was added and the mixture was heated at 70°C for 15 minutes, yielding 60 - 70% of the desired compound as determined by HPLC. Chromatographic purification of the reaction mixture on PRP-1 resin yielded the product in >90% purity.

Example 38 Preparation of 99mTcCl ( CDO ) 2 ( QNB-boron ) Into a 5 ml siliconized serum vial were measured 2.0 mg of 1 , 2-cyclohexanedione dioxime, 1.5 mg of 3-quinuclid nyl- (4-borono-benzilate ) (QNB-boronic acid), 20 mg of citric acid, 100 mg of NaCl, 2.0 mg of diethylenetriaminepenta-acetic acid, and 125 pg of SnCl, (in 4M HCL) in a total volume 0.7 ml of 28% ethanol/sal ine . 0.5 ml of 99m Tc04~ generator eluent was added and the mixture was heated at 70°C for 15 minutes, yielding 83% of the desired compound as determined by HPLC. Chromatographic purification of the reaction mixture on PRP-1 resin yielded the product in >90% purity.

ST l'CTURES OF BORONIC ACFDS IN THE EXA fPLES

Claims (13)

WHAT IS CLAIMED IS:

1. A nitro-heterocyclic compound of the formul 10 15 or wherein the ring portion is a 5- or 6-membered cyclic or aromatic ring; n is the total number of substitution 25 positions available on said 5- or 6-membered ring; said one or more R groups are independently hydrogen, halogen, alkyl, aryl, alkoxy, oxa-alkyl, hydroxyalkoxy, alkenyl, arylalkyl, arylalkylamide, alkylamide, alkyla ine and (alkylamine)alkyl; 30 Xj is nitrogen, sulfur, oxygen, -CR= or -CRR-; and (Ax ) can be absent when p is zero in which case said ring is linked to the boron atom via a nitrogen or carbon atom, or (Αχ)^, when p is an 35 integer greater than zero, comprises the linX - 74 - 114,175/2 between said ring and the boron atom; wherein Αχ, or the various Α units in forming a straight or branched chain if p > 1, are independently selected from -CH2-, -CHR4-, -CR4RS-, -CH=CH=, -CH=CR4-, -CR4=CR5-, -C≡C- , cycloakyl, 0 II. cycloalkenyl, aryl, heterocyclo, oxygen, sulfur, -C-, -NH-, -HC=N- , -CR4=N, -NR4- , -CS-; wherein R4 and R5 are independently selected from alkyl, alkenyl, alkoxy, aryl, 5- or 6-membered nitrogen or oxygen containing heterocycle, halogen, hydroxy or hydroxyalkyl ; and wherein Rv and R-,' are each independently hydrogen, alkyl, or aryl, or where RT and R7' taken together are -(CReR9 ) 2_6- and Ra and R9 are independently hydrogen or alkyl .

2. A compound of claim 1, wherein said ring portion is a 2-, 4-, or 5-nitroimidazole, a nitrofuran or a nitrothiazole, including derivatives thereof.

3. A compound of claim 1, wherein said ( ) v is absent or is selected from alkyl, alkyl with one or more ether linkages, hydroxyalkyl, hydroxyalkoxy, alkenyl, arylalkyl, arylalkylamide , alkylamide, alkylamine and ( alkylamine ) alkyl .

4. A compound of claim 1, wherein said ring portion 2-nitroimidazole ; (Aj ) is selected from -(CH2)2_3- 0 II -CH2-CH=CH-CH2-, -(CH2 ) ^-C-NH- ( CH2 )1_3', 2OCH2-, -(A3-NH-A3 · )1_3* wherein A3 and A3 ' are the same or different alkyl .

5. A compound of claim 1, having the name l-(2-nitroimidazole ) -benzylboronic acid .

6. A compound of claim 1, having the name 4-(2-nitro-imidazolyl ethyl) phenyl boronic acid.

7. A compound of claim 1, having the name 2-nitro-imidazolyl-Nj.- [ 2-propenyl] -3-boronic acid (BpropenN02 ) .

8. A compound of claim 1, having the name 2-nitro-imidazolyl- N^-propyl-S-boronic acid (BpropN02).

9. A compound of claim 1, having the name l-(4-nitro-imidazole) -benzylboronic acid (BB4N02).

10. A compound of claim 1, having the name (R)-l-aza-bicyclof 2 , 2 , 2 ] oct-3- yl- (R) -α-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (R,R-QNB boronic acid).

11. A compound of claim 1, having the name (S)-l-aza-bicyclo[2,2,2]oct-3-yl- ( ) -α-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (R,S-QNB boronic acid).

12. A compound of claim 1, having the name (S)-l-aza-bicyclo [ 2 , 2 , 2 ] oct-3-y1- ( S ) -α-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (S,S-QNB boronic acid).

13. A compound of claim 1, having the name (R)-l-aza-bicyclo[2,2,2] oct-3-yl- ( S ) -α-hydroxy-a- ( 4 ) -phenylboronic acid-a-phenylacetate (S,R-QNB boronic acid). for the Applicant: WOLFF, BREGMAN AND GOLLER