BACKGROUND OF THE INVENTION

Radiopharmaceutical chelate systems have been used to couple with peptides and proteins, for the purpose of diagnostic imaging. Many such chelate systems have a central "N2S2", "N3S3" moiety; a few have a "N3S2" moiety.

The N3S2 containing system is preferred due to the combination of one central alkyl amino group and two other alkyl/amide nitrogens and two thiols which are responsible for the chelating properties, and which form stable compounds with Group Vllb metals at reasonable temperatures (i.e., <_60°C) and which also allow simple attachment to peptides and proteins under aqueous conditions.

SUMMARY OF THE INVENTION

The present invention relates to novel N3S2 chelating ligands and a process for their production. These are useful for attachment to peptides and proteins, and thereafter chelated with appropriate radio metallic isotopes for treatment of appropriate receptor positive tumors or as in vivo diagnostic imaging agents.

These chelates are "N3S2" type compounds of the following structure:

wherein R is hydrogen, loweralkyl of 1-4 carbon atoms, or loweralkyl carboxyl, wherein loweralkyl is 1-4 carbon atoms; R! is hydrogen, a suitable protecting group such as p-loweralkyloxyl (1-4 carbon atoms) benzyl such as p-methoxylbenzyl; trityl; or R* and Rl are linked together to form a bond between the two "S" groups;

and R2 is either a free amino or an isothiocyanato group, which can be

=C=S or — H ₂ ;

and n or m are independently an integer from 1-4.

These ligands are prepared by using either a cyclic approach, when R1 and R are linked together to form the disulfide bond; or an open chain approach when Rl and Rl are either hydrogen or the protecting group.

The cyclic approach reacts a tris(2-aminoethyl)amine with the appropriate dithio-dialdehyde in a suitable solvent such as lower alkanol at reflux. Thereafter, the cyclic amine is optionally reacted on the secondary amine groups, to provide the desired R groups, and subsequently with the appropriate N-hydroxy succinimide ester in triethylamine and dichloromethane to yield compounds in which R2 is

the amino group; and subsequently optionally reacted with thiophosgene to yield the corresponding isothiocyanato derivatives.

The open chain approach utilizes a diethylenetriamine reaction with first phthalic anhydride; second, p-nitrobenzyl bromide; and third, 6N HC1 at reflux to yield the appropriate N'-(4-nitrobenzyl)- bis-(2'-phthalimidoethyl)amine, to which subsequently the pendent blocking groups are attached, followed by reaction of the amino group to isothiocyanato if desired.

The novel N3S2 ligands can then be labelled with the appropriate radioisotope by reacting with the radioisotope in the form of a transfer chelate such as a glucoheptonate complex (available commercially) and heating at 40-80°C for 1-4 hours. Alternatively, the N3S2 ligands can be coupled with the appropriate peptide or protein and then radiolabelled using a similar procedure. After labelling, the N3S2 ligands are useful as radioimaging agents or as radio therapeutic agents for the treatment of appropriate tumors. When the ligands are to be first coupled with the peptide or protein, the isothiocyanate group at R2 is first prepared for reaction with the amino group of the peptide or protein; and thereafter chelated with the appropriate radioisotope.

The preferred peptide or protein to be used includes natural and synthetic somatostatin and analogues, atrial natriuretic factor peptides, fibrin binding domain peptides, and monoclonal antibodies or fragments thereof, F(ab)2, Fab, Fv regions; oxytocin; substance P; vasopression; as well as any peptidomimetics containing an amino group. The preferred radioisotope is one of those of rhenium or technetium, preferably Re- 186, Re- 188 or Tc-m99.

Other radio isotopes can be used which can be any detectable element. By detectable element is meant any element, preferably a metal ion which exhibits a property detectable in therapeutic or in vivo diagnostic techniques, e.g., a metal ion which emits a detectable radiation or a metal ion which is capable of influencing NMR relaxation properties, and which is capable of forming a chelate with the N3S2 system-

Suitable detectable metal ions include, for example heavy elements or rate earth ions, e.g., paramagnetic ions, e.g., Gd3 ⁺ , Fe^+, Mn2+ and Cr^+, fluorescent metal ions, e.g., Eu3+, and radionuclides, e.g., γ-emitting radionuclides, β-emitting radionuclides, α-emitting radionuclides, positron-emitting radionuclides, e.g., 68Ga.

The products of this invention are useful either as a diagnostic imaging agent, e.g., visualization of the particular (peptide) receptor positive tumors and metastases when complexed with a paramagnetic, a γ-emitting metal ion or a positron-emitting radionuclide, or as a therapeutic radiopharmaceutical for the treatment in vivo of

(peptide) receptor positive tumors and metastases when complexed with α- or β-radionuclide, as indicated by standard tests.

The particular radioisotope chosen is relevant to the organ o system to be radioimaged. For instance, in the last few years a high incidence of somatostatin receptors has been demonstrated in a variety of human tumors, e.g., pituitary tumors, central nervous system tumors, breast tumors, gastoenteropancreatic tumors and their metastases. Some of them are small or slow-growing tumors which are difficult to precisely localize by conventional diagnosis methods, but in vitro visualization of somatostatin receptors has been performed through autoradiography of tumoral tissues using radioiodinated somatostatin analogues.

The products of this invention when used as imaging agents may be administered parenterally, preferably intravenously, e.g., in the form of injectable solutions or suspensions, preferably in a single injection. The appropriate dosage will of course vary depending upon, for example, the precise chelating ligand and the type of detectable element used, e.g., the radionuclide. A suitable dose to be injected is in the range to enable imaging by photoscanning procedures known in the art. It may advantageously be administered in a dose having a radioactivity of from 0.1 to 50 mCi, preferably 0.1 to 30 mCi, more preferably 0.1 to 20 mCi. An indicated dosage range may be of from 1 t 200 μg product labelled with 0.1 to 50 mCi, preferably 0.1 to 30 mCi, e.g., 3 to 15 mCi, γ-emitting radionuclide, depending on the γ-emitting radionuclide used.

The enrichment in the tumorigenic sites with the products may be followed by the corresponding imaging techniques, e.g., using nuclear medicine imaging instrumentation, for example a scanner, planar or rotating γ-camera, each preferably computer assisted; PET-scanner (Positron emission tomography) or MRI equipment.

These products can also be used for in vivo treatment of peptide receptor positive tumors and metastases in a subject in need of such a treatment which comprises administering to said subject a therapeutically effective amount of the product. Dosages employed in practicing the therapeutic method of the present invention will of course vary depending, e.g., on the particular condition to be treated, for example the volume of the tumor, the particular product employed, for example the half-life of the product in the tumor, and the therapy desired. In general, the dose is calculated on the basis of radioactivity distribution to each organ and on observed target uptake. For example, the product may be administered at a daily dosage range having a radioactivity of from 0.1 to 3 mCi kg body weight, e.g., 1 to 3 mCi, preferably 1 to 1.5 mCi/kg body weight. An indicated daily dosage range is of from 1 to 200 μg ligand labelled with 0.1 to 3 mCi/kg body weight, e.g., 0.1 to 1.5/kg body weight a- or β-emitting radionuclide, conveniently administered in divided doses up to 4 times a day.

These products may be administered by any conventional route, in particular parenterally, e.g., in the form of injectable solutions or suspensions. They may also be administered advantageously by infusion, e.g., an infusion of 30 to 60 min. Depending on the site of the tumor, they may be administered as close as possible to the tumor site, e.g., by means of a catheter. The mode of administration selected may depend on the dissociation rate of the product used and the excretion rate. These products may be administered in free form or in pharmaceutically acceptable form, such as salts which may be prepared in conventional manner and exhibit the same order of activity as the free compounds.

The products for use in the method of the present invention may preferably be prepared shortly before the administration to a subject, i.e., the radiolabelling with the desired detectable metal ion, particularly the desired α-, β- or γ- radionuclide, may be performed shortly before the administration.

They are then suitable for imaging or treating tumors such as pituitary, gastroenteropancreatic, central nervous system, breast, prostatic, ovarian or colonic tumors, small cell lung cancer, paragangliomas, neuroblastomas, pheochromocytomas, medullary thyroid carcinomas, myelomas, etc. and metastases thereof, as well as lymphomas.

According to a further aspect of the invention, there is provided: i. a pharmaceutical composition comprising the radiolabelled product of the invention in free or in pharmaceutically acceptable salt form, together with one or more pharmaceutically acceptable carriers or diluents therefor; or

ii. a pharmaceutical composition comprising a chelate- peptide product according to the invention in free or in pharmaceutically acceptable salt form, together with one or more pharmaceutically acceptable carriers or diluents therefor.

Such compositions may be manufactured in conventional manner.

A composition according to the invention may also be presented in separate package with instructions for mixing the chelate- peptide product with the metal ion and for the administration of the resulting radiolabelled product. It may also be presented in twin-pack form, that is, as a single package containing separate unit dosages of the ligand and the detectable metal ion with instructions for mixing them and

for administration of the product. A diluent or carrier may be present in the unit dosage forms.

A preferred use of the N3S2 ligands of this invention is then coupling to a novel synthetic somatostatin receptor-binding peptide. The best somatostatin receptor-binding peptide is a synthetic hexapeptide.

Me \ / Tyr Phe

Lys^ J-ys

Val

wherein Phe, Tyr, Trp, Lys, Val, and Lys are the usual amino acids. This and other suitable peptides are disclosed in Tet. Letters, Vol. 22, No. 36, pp. 4675-4678, 1991. This cyclic hexapeptide can be linked via the isothiocyanato moiety to any of the N3S2 ligands in this application, and then labelled with Tc-99. The chelated and/or radiolabelled product is not a part of this invention, but is disclosed and claimed in a separate application, Attorney docket Case 19312, filed simultaneously with the instant application.

EXPERIMENTAL

Materials and methods. Unless otherwise specified, all reactions were carried out in oven-dried flasks at room temperature under an argon atmosphere with magnetic stirring. After extraction, organic solvents were dried over MgSθ4, filtered, and removed under reduced pressure on a rotary evaporator. Reagent grade solvents, starting materials and deuterated solvents were purchased from Aldrich Chemical Co. (Milwaukee, WI) and used without further purification.

^H NMR spectra were obtained on a Bruker Model AM 500, AM 400, and AM 300. Samples were dissolved in CDCI3, MeOD4, or DMSO-d6 and chemical shifts were reported as δ values with the solvent or tetramethylsilane resonance as the internal standard. The multiplicity

is defined by s(singlet), d(doublet), t(triplet), q(quartet), and m(multiplet). The relative peak heights of the resonances are reported as integers following the multiplicity. ^C NMR spectra were recorded on a Bruker AM-300 spectrometer at 75.5 MHz and the degree of substitution of each carbon atom was determined by complete decoupling and DEPT composed 135° pulsed sequence experiments. For l-^C the carbon and proton signals were assigned by heterocorrelation experiments.

Infrared(IR) spectra (solution cells-CDCl3 as solvent) were recorded on a Perkin Elmer 681 infrared spectrophotometer. Melting points were determined on a Thomas Hoover capillary melting point apparatus and are uncorrected. Mass spectra(MS) were recorded either in the CI(methane gas) or FAB mode using Finnigan 4500 single quadrupole mass spectrometer and were run by Oneida Research Services, Inc. (Whitesboro, NY). Flash chromatography was performed essentially as described in the literature 1 using Merck silica gel 60 (230- 400 mesh) as stationary phase with the use of the following solvents: methanol(M), methylene chloride(C), ammonium hydroxide(H).

Part 1: Cyclic Approaches to N3S Chelates

Synthesis of N^S -isothiocyanate (i n TPPBI

3,3,13,13-Tetramethyl-l,2-dithia-5,8,l l-triazacyclotridecan-8-yl- ethanamine (4) A round bottom flask was charged with tris(2-aminoethyl)- amine (1) (989 mg, 6.76 mmol), α,α'-dithiodiiso-butyraldehyde (2) (1,380 mg, 6.69 mmol prepared according to reference 2b) and ethanol (200 ml). The mixture was stirred at room temperature for 1.5 hours and then refluxed for 3 hours. After cooling the volatile materials were removed in vacuo to give the crude di-imine as a glassy solid. *H

NMR analysis of the di-imine 2 gave three singlets centered at 7.58 ppm (17:67:17) confirming the formation of an imine.

To the crude di-imine 2. in refluxing ethanol (200 mL) was added sodium borohydride (1.346 g, 35.58 mmol) in two portions over

3.5 hours. The reaction mixture was refluxed for a total of 17 hours and acetone (100 ml) was added to destroy excess reagent. After cooling the solvent was removed in vacuo, water was added, and the product was extracted with 5% MeOH CH2CL2. The organic layer was dried (MgSθ4), filtered, and concentrated in vacuo to give a yellow oil. Flash chromatography of this oil using 82.5% C/15.0% M/2.5% H gave amine 4 as a light yellow viscous oil (1.268 g, 59.5% yield). lH NMR (in CDCI3): δ 2.83 (t,j=5.9 Hz,2H,N-CH2CH2-NH2), 2.72 (s,4H,2N-CH2-C-S), 2.70 (m,4H,2N-CH2CH2-NH), 2.58 (m,4H,2N- CH2-CH2-NH), 2.50 (t,j=5.9 Hz,2H,N-CH2CH2-NH2), 1.73 (br s,4H,4NH), 1.33 (s,12H,4CH3-C-S) ppm. 13c NMR (in CDCI3): 59.2 (t,2NH-CH2-C-S), 56.6 (t,N-CH2CH2-NH2), 54.5 (t,2N-CH2CH2-NH), 50.5 (s,2CH3-C-S), 47.4 (t,2N-CH2CH2-NH), 39.6 (t,N-CH2CH2-NH2), 27.4 (q,4CH3-C-S) ppm. MS (m/z,CI): 321(100, M++1). IR (CDCI3): 3350, 2940, 2820, 1455, 1360, 1120 cirri.

3,3, 13, 13-Tetramethyl- 1 ,2-dithia-5,8, 11 -triazacyclotridecan-8-yl-(2'-N- phthaloyl Vethanamine (5)

A round bottom flask was charged with amine 4 (111.2 mg, 0.347 mmol), N-carboethoxyphthalimide (108.3 mg, 0.494 mmol), and dichloromethane (10 mL). The reaction mixture was stirred at room temperature for 1 hour and the solvent was removed in vacuo. Flash chromatography of the residue using 90% C/9.5% M/0.5% H gave the phthalate 5 as a yellowish oil (119.2 mg, 76.3%). iH NMR (in CDCI3): δ 7.86 (m,2H,H2&H5-Ar), 7.71 (m,2H,H3&H4- Ar), 3.84 (t,j=6.4 Hz,2H,N-CH2CH2-NPhth), 2.81 (t,j=6.4 Hz,2H,N- CH2CH2-NPhth), 2.69 (m,4H,2N-CH2CH2-NH), 2.66 (m,4H,2N- CH2CH2-NH), 2.59 (s,4H,2N-CH2-C-S), 1.87 (br m,2H,2NH), 1.23 (s,12H,4CH3-C-S) ppm. 13c NMR (in CDCI3): 168.1 (s,2CO), 133.7 (d,C3&C4-Ar), 131.9(s,Cl&C6-Ar), 123.3 (d,C2&C5-Ar),58.7(t,2NH- CH2-C-S),53.9(t,2N-CH2CH2-NH),52.8 (t,N-CH2CH2-NPhTh),50.2 (s,2CH3-C-S),47.6(t,2N-CH2CH2-NH),35.8 (t,N-CH2CH2-NPhTh), 27.3(q,4CH3-C-S)ppm. MS (m/z,CI):451(100,M++1). IR(CDCI3): 3400,2950,2810, 1770, 1705, 1465, 1395cm-1.

3,3,5,11,13, 13-Hexamethy 1-1, 2-dithia-5, 8,11 -triazacyclotridecan-8-yl- ethanamine (1)

A round bottom flask was charged with phthalate _ (775.7 mg, 1.72 mmol), formic acid (10 mL, 265 mmol), and formaldehyde (37% wt in water, 15 mL, 200 mmol). The reaction mixture was refluxed for 20 hours and then allowed to cool and the solvent was removed in vacuo. A solution of 10% KOH was added to the solid residue and the compound extracted with 5% MeOH/CH2CL2- The organic solvent was dried (MgS04), filtered, and concentrated in vacuo to give crude 6 as a viscous oil.

To a round bottom flask was added crude _,, hydrazine monohydrate (1 mL, 20.6 mmol), and ethanol (40 mL). The reaction mixture was refluxed for 20 hours and then allowed to cool. The solvent was removed in vacuo, water added, and the residue extracted with 5% MeOH/CH2CL2- The organic solvent was dried (MgS04), filtered, and concentrated in vacuo to give a yellowish viscous oil. Flash chromatography of the crude product using 80% C/19.5% M/1.0% H gave dimethyltetramine 7 as a light yellow oil (375 mg, 62.4% overall yield from 4). lH NMR (in CDCI3): δ 2.78 (t,j=5.9 Hz,2H,N-CH2CH2-NH2), 2.72 (t,j=5.5 Hz,4H,2N-CH2CH2-NCH3), 2.63 (s,4H,2N-CH2-C-S), 2.60 (t,j=5.5 Hz,4H,2N-CH2CH2-NCH3), 2.42 (t,j=5.9 Hz,2H,N-CH2CH2- NH2), 2.36 (s,6H,2NCH3), 1.77 (br s,2H,NH2), 1.28 (s,12H,4CH3-C-S) ppm. 13c NMR (in CDCI3): 67.2 (t,2N-CH2-C-S), 57.9 (t,2N-CH2CH2- NCH3), 55.6 (t,N-CH2CH2-NH2), 52.1 (1.2N-CH2CH2-NCH3), 51.3 (s,2CH3-C-S) 45.1 (q,2NCH3), 39.5 (t,N-CH2CH2-NH2), 27.4 (q,4CH3- C-S) ppm. MS (m/z,CI): 349(100,M++1). IR (CDCI3): 2960, 2800, 1455, 1355, 1310, 1100 cm-1.

4-Amino-N-[2-(3,3,5, 11,13,13-hexamethyl- 1 ,2-dithia-5,8, 11-triazacyclo- tridecan-8-yl ^' )ethylibenzamide ⁽ 10 ^{^} 1

A round bottom flask was charged with the dimethyl¬ tetramine 7 (514.9 mg, 1.48 mmol), tBoc-p-aminobenzoyl N-

hydroxysuccinimide ester (_) (493.8 mg, 1.48 mmol, prepared according to reference 3), triethylamine (0.21 mL, 1.51 mmol), and dichloromethane (40 mL). The reaction mixture was stirred at room temperature for 12 hours and the solvent was removed in vacuo to give crude 2.

To a round bottom flask was added crude _\, dichloro¬ methane (10 mL), and trifluoroacetic acid (10 mL) and the resulting mixture was stirred at room temperature for 1 hour. The solvent was removed in vacuo and purification by flash chromatography of the residue using 94.5% C/ 5.0% M/0.5% H gave the aniline \_ as a yellowish white solid (345.8 mg, 50.8% overall yield from dimethyltetramine 7). lH NMR (in CDCI3): δ 7.65 (d,j=8.6 Hz,2H,H2&H6-Ar), 6.87 (br s,lH,NH-CO), 6.67 (d,j=8.6 Hz,2H,H3&H5-Ar), 3.95 (s,2H,NH2), 3.49 (t,j=5.4 Hz,2H,N-CH2CH2-NCO), 2.74 (m,4H,2N-CH2CH2-NCH3),

2.65 (m,4H,2N-CH2CH2-NCH3), 2.61 (s,4H,2N-CH2-C-S), 2.53 (t,j=5.4 Hz,2H,N-CH2CH2-NCO), 2.30 (s,6H,2NCH3), 1.29 (s,12H,4CH3-C-S) ppm. 13C NMR (in CDCI3): 167.1 (s,NHCO), 149.6 (s,Cl-Ar), 128.6 (d,C3&C5-Ar), 123.9 (s,C4-Ar), 113.9 (d,C2&C6-Ar), 67.2 (t,N-CH2-C- S), 57.6 (t,2N-CH2CH2-NCH3), 53.7 (t,N-CH2CH2-NHCO), 53.4

(s,2CH3-C-S),51.4(t,2N-CH2CH2-NCH3)45.0(q,2NCH3),37.0(t,N - CH2CH2-NHCO),27.2(q,4CH3-C-S)ppm. MS(m/z,FAB):468.2(100, M++1). IR(CDCI3): 3405,2960,2800, 1620, 1495, 1280, 1100, 835 cm-l.

4-Isothiocyanato-N-[2-(3,3,5, 11 , 13, 13-hexamethyl- 1 ,2-dithia-5,8, 11 - triazacyclotridecan-8-yl)ethyl1benzamide (11) ITPPBII

To a round bottom flask with the aniline 1Q (53.3 mg, 0.114 mmol) and dichloromethane (5 mL) was added 0.2007 M solution of thiophosgene (0.60 mL, 0.120 mmol) in dichloromethane. The heterogeneous reaction mixture was stirred at room temperature for 1 hour and the solvent was removed in vacuo to give the isothiocyanate ϋ as a reddish solid (67.8 mg, 116%).

iH NMR (in DMSO-d6): δ 8.88 (br s,lH,NH-CO), 7.99 (d,j=8.4 Hz,2H,H2«feH6-Ar), 7.54 (d,j=8.4 Hz,2H,H3&H5-Ar), 3.49 (m,2H,N- CH2CH2-NCO), 3.40 (m,8H,2N-CH2CH2-NCH3), 3.01 (s,4H,2N-CH2- C-S), 2.89 (s,6H,2NCH3), 2.71 (m,2H,N-CH2CH2-NCO), 1.45 (s,12H,4CH3-C-S) ppm. MS (m/z,CI): 510(100, M++1). IR (CDCI3) : 3400, 2960, 2100, 1640, 1600, 1545, 1500, 1470, 1300 cm"l.

Preparation of Somatoscan(Fmoc)TPPBI (13

In a 5 mL Reacti-Vial (Pierce) a solution of Somatoscan- Fmoc (12) [cyclo(Trp-Lys(Fmoc)-Val-Lys-NMe-Phe-Tyr)] (1.97 mg; 1.515 umol), TPPBI (11) (8.4 mg, 16.495 umol), and DMF (400 μL) was stirred while bicarbonate/phosphate buffer (0.2 M, pH 8.2, 100 μL, freshly prepared) was added. The heterogeneous solution was monitored by HPLC and stirred for 4 hours at room temperature. The solvents were removed in vacuo and the residue was partitioned with IN HCl (300 μL) and MeOH (100 μL). Purification of this solution by HPLC (Hamilton PRP-1 12-20 μm preparative column 250 x 21.5 mm) using a 30% to 100% gradient of acetonitrile : water (containing 0.1% TFA) over 40 minutes (flow rate of 12 mL/min) afforded pure Somatoscan(Fmoc)- TPPBI (11) (R _t = 20.64 min).

MS (Electrospray, Hypermass) 799.4(z=2), Calc. Compound Mass = 1596.8, Meas. Compound Mass = 1597.8.

Part 2: Acyclic Approaches to N3S Chelates

Synthesis of Acyclic Dimercaptoanisidine Arylisothiocyanates

Synthesis of open chain ^S -aryl isothiocvanate (21)

Bis(2'-phthalimidoethyl)amine. ( 15)

This was prepared according to reference 4.

Phthalic anhydride (32 g; 0.22 mol) was dissolved in 333 mL of hot chloroform and the mixture was filtered to eliminate phthalic acid . A Diethylenetriamine 14 (7.97 g; 0.077 mol) solution in

chloroform (64 mL) was slowly added (over a period of 50 minutes) to the phthalic anhydride mixture maintained at a temperature of 50°C. Temperature was raised to 110°C after the addition was over. The reaction mixture was then stirred for 48 hours and slowly concentrated. The concentrate solution was then treated with activated charcoal. 31.8 g of a yellow solid was recovered after evaporation of the solvent under reduced pressure. The solid was triturated successively with ether, ethanol and then dissolved in methylene chloride. The methylene chloride solution was washed with 10% sodium carbonate (3 x 500 mL), water and saturated sodium chloride solution. The organic phase was dried with magnesium sulfate, filtered and evaporated to dryness under reduced pressure. A pale yellow solid (14.47 g; 52%) was obtained. A portion (4.45 g) of that product was purified by flash chromatography (silica gel) using a mixture of methylene chloride, ethyl acetate and triethylamine as elution system (79/20/1). The purification give 2.798 g of bis(phthalimidoethyl)amine (15).

6.96 g of phthalic acid was recovered. iH NMR (in CDCI3): δ 7.70 (m,8H,H-Ar(phth)), 3.77 (t,J=6Hz,4H, -NH(-CH2-CH2-NPhth)2), 2.95 (t,J=6Hz,4H,-NH(-CH2-CH2-NPhth)2), 1.41 (broad,lH,-NH(-CH2-CH2-NPhth)2) ppm. IR (in CDCl3/NaCl): 3460 (N-H,w, sec amine), 2940-2820 (C-H), 1770-1710 (C=0, Phth), 1465, 1425, 1390, 1360, 1185, 1035 cπrl. MS (El; m/z): 363(0.4,M+), 364(4,M++1), 216(3,M+-Phth), 204(18), 203(100,M+-(Phth-CH2 ^# )), 174(57,Phth-CH2-CH2 ⁺ ), 160(5), 147(6), 130(12) and 56(6).

vV'-(4-Nitrobenzyl) bis(2'-phtalimidoethyl)amine (16)

(See Ref. 4) In a 250 mL round bottom flask potassium hydroxyde (1.6 g; 28 mmol) was dissolved in hot ethanol (100 mL). To that ethanolic solution Bis(2'-phthalimidoethyl)amine Q_Y) (10.02 g; 28 mmol) was added. The solution was magnetically stirred and refluxed for 2 1/2 hours before p-nitrobenzyl bromide (5.95 g; 28 mmol; 1 eq) was added. The reaction mixture was heated at reflux for 16 additional hours then filtered hot. The solid obtained previously was washed with absolute ethanol and dried under vacuum to yield 7.441 g (54%) of a

white solid (p-nitrobenzyl bisphthalimide). The filtrate was evaporated under reduced pressure to give 8.19 g of a yellow solid. That residue was purified by flash chromatography (silica gel: 400 g) using methylene chloride-methanol (98/2) system as eluent. The purification by chromatography produced 3.13 g (23%) of the desired product. The alkylation reaction yielded 10.571 g of N'-(4-nitrobenzyl) bis(2'- phtalimidoethyl)amine. (16) lH NMR (in CDCI3): δ 7.70 (m,10H,H-Ar(Phth)+o(H)-Ar-Nθ2), 7.20 (d, J=9Hz,2H, m(H)-Ar-Nθ2), 3.75 (t, J=6Hz, 4H,-NH (-CH2-CH2-NPhth)2), 3.71 (s, 2H,-N-CH2-Ar-Nθ2) and 2.80 (t,

J=6Hz,4H,-NH(-CH2-CH2-NPhth)2) ppm. MS (El; m/z): 498(1, M+), 499(0.6,M++1), 362(l,M+- ^* CH2Ar-N02), 339 (32, M++l-(Phth-CH2 ^* )), 338 (100, M+-(Phth-CH2')), 324 (2, M+-(Phth-CH2-CH2*)), 174(58,Phth-CH2-CH2+), 173(42), 165(6), 163(8), 161(6), 160(43), 149(12), 136(24), 130(12), 106(21), 105(12), 104(17), 90(22), 89(18), 78(23), 77(21) and 76(12).

Hydrolysis of _V'-(4-nitrobenzyl) bis(2'-phtalimidoethyl)amine

In a 250 mL round bottom flask, provided with a condenser, N'-(4-nitrobenzyl) bis(2'-phtalimidoethyl)amine (1_) (2.80 g; 5.62 mmol) and 6 N hydrochloric acid (150 mL) were introduced. The reaction mixture was stirred and refluxed for 23 hours. The solution was cooled with an ice bath and filtered. The filtrate was washed with ether (3 x 100 mL) and dried by vacuum to give a yellow foam-like material (2.17 g). The residue was dissolved in water (10 mL) and the pH of that solution was brought basic with 1 N sodium hydroxide (25 mL). Then the mixture was extracted with methylene chloride (3 x 75 mL). The organic extracts were combined, dried with magnesium sulfate, filtered and evaporated to dryness to yield 1.347 g of N'-(4-nitrobenzyl) bis(2'- aminoethyl)amine (17) as a light orange oil (which turn dark red with time).

Note: The p-nitrobenzyltriamine (17) is stored for short term away from light and in an inert atmosphere of argon. For long term storage it is better to keep that compound as the hydrochlorate form.

iH-NMR (in CDCI3): δ 8.13 (d,J=9Hz,2H,o(H)-Ar-N02), 7.46 (d, J=9Hz, 2H,m(H)-Ar-N02), 3.65 (s,2H,-N-CH2-Ar-Nθ2), 2.74 (t,J=6Hz, 4H, -N(-CH2-CH2-NH2)2), 2.50 (t,J=6Hz,4H,-N(-CH2-CH2-NH2)2) and 1.43 (broad s, 4H, -N(-CH2-CH2-NH2)2) ppm. IR (film): 3370-3290 (N-H,-NH2), 2940-2800(C-H), 1605 (C=C,Ar), 1510 (N=0,Ar), 1450, 1340 (N=0,Ar), 1105, 1010, 850 (C-N,Ar-Nθ2) and 730 cm-1.

N'-4- Aminobenzyl-diethylenetriamine (18)

This was prepared according to reference 4. lH NMR (in CDCI3): δ 7.08 (d,j=8.3 Hz,2H,H3&H5-Ar), 6.64 (d,j=8.3 Hz,2H,H2&H6-Ar), 3.62 (br s,2H,Ar-NH2), 3.48 (s,2H,N-CH2-Ar), 2.74 (t,j=6.0 Hz,4H,2N-CH2CH2-NH2), 2.50 (t,j=6.0 Hz,4H,2N-CH2CH2- NH2), 1.52 (br s,4H,2NH2) ppm.

N,N"-Bis[2-((4-methoxybenzyl)Aio)-2-methyl-propionyl]-N'- (4- aminobenzvD-diethylenetriamine (20)

To a solution of the aniline __, (230 mg, 1.10 mmol, freshly prepared) in ethanol (20 mL) was added a solution of 2-[(p-methoxy- benzyl)thio]-2-methylpropionic acid chloride 19 (1.33 g, 5.10 mmol, prepared according to reference 5) in dichloromethane (10 mL) over 15 minutes. The resulting solution was stirred for 48 hours and the solvent was removed in vacuo, 1 N NaOH was added, and the product was extracted with CH2CI2. The organic layer was washed with water, dried (MgS04), filtered, and concentrated in vacuo to give a red oil. Flash chromatography of this oil using 5% MeOH CH2Cl2 gave the aniline 20 as a yellow oil (126. mg, 17.5% yield). lH NMR (in CDCI3): δ 7.15 (d,j=8.6 Hz,4H,2H3&H5-Ar-OCH3), 7.07 (t,j=8.2 Hz,2H,H3&H5-Ar-NH2), 7.07 (m,2H,2NHCO), 6.78 (d,j=8.6 Hz,4H,2H2&H6-Ar-OCH3), 6.58 (d,j=8.2 Hz,2H,H2&H6-Ar-NH2), 3.74

(s,6H,2CH3θ), 3.72 (br s,2H,NH2), 3.65 (s,4H,2S-CH2-Ar), 3.49 (s,2H,N-CH2-Ar), 3.24 (q,j=5.9 Hz,4H,2N-CH2CH2-NHCO), 2.55 (t,j=6.2 Hz,4H,2N-CH2CH2-NHCO), 1.50 (s,12H,4CH3-C-S) ppm. 13c NMR (in CDCI3): δ 174.6 (s,2NCO), 158.9 (s,2Cl-Ar-OCH3), 146.0 (s,Cl-Ar-NH2), 130.2 (d,C3&C5-Ar-NH2 + 2C3&C5-Ar-OCH3), 129.6 (s,2Cl«&C4-Ar-OCH3), 129.1 (s,C4-Ar-NH2), 115.4 (d,C2&C6-Ar- NH2), 114.3 (d,2C2&C6-Ar-OCH3), 58.3 (t,N-CH2-Ar), 55.5 (q,2CH3θ), 53.0 (t,2N-CH2CH2-NHCO), 50.3 (s,2S-C-CH3), 37.8 (t,2N-CH2CH2-NHCO), 34.4 (t,2S-CH2-Ar), 27.1 (q,4CH3-C-S) ppm. MS (m/z,FAB): 653.5(100, MH+). IR (CDCI3): 3380, 3000, 2930, 2835, 1665, 1510, 1245, 1195, 1175, 1035 cm"l .

N,N"-Bis[2-((4-memoxybenzyl)thio)-2-memyl-propionyl]-N'-( 4- isothiocvanatobenzvD-diethylenetriamine (21) To a round bottom flask with the aniline 20 (55.7 mg,

0.0853 mmol) and dichloromethane (5 mL) was added 0.2011 M solution of thiophosgene (0.42 mL, 0.0845 mmol) in dichloromethane. The heterogeneous reaction mixture was stirred at room temperature for 1 hour and the solvent was removed in vacuo to give the isothiocyanate 21 as a brown solid (68.9 mg, 116%). lH NMR (in CDCI3): δ 7.72 (m,2H,2NHCO), 7.65 (d,j=8.3 Hz,2H,H2&H6-Ar-NCS), 7.25 (t,j=8.3 Hz,2H,H3&H5-Ar-NCS), 7.17 (d,j=8.5 Hz,4H,2H3&H5-Ar-OCH3), 6.80 (d,j=8.5 Hz,4H,2H2&H6-Ar- OCH3), 4.14 (s,2H,N-CH2-Ar), 3.77 (s,6H,2CH3θ), 3.70 (s,4H,2S- CH2-Ar),3.58 (m,4H,2N-CH2CH2-NHCO),3.01 (m,4H,2N-CH2CH2- NHCO), 1.53 (s,12H,4CH3-C-S)ppm. IR(CDCI3): 3300,2930,2080, 1655, 1605, 1510, 1245, 1170, 1030cπrl.

Part 3: Synthesis of acyclic dimercaptoanisidine alkyl isothio- cyanates

Synthesis of open chain N3S2-alkylanisidine 26

N,N-Bis(2-aminoethyl)-N'-tert-butyl-oxycarbonyl- 1 ,2-ethanediamine

(22)

A solution of tris(2-aminoethyl)amine (1) (19.5 g, 133.6 mmol) in CH2CI2 (300 mL) was cooled to -78°C in a dry ice-acetone bath while di- rt-butyl dicarbonate (14.6 g, 66.9 mmol) in CH2CI2 (100 mL) was added slowly over 30 minutes. The reaction mixture was slowly allowed to warm up to room temperature and stirred for 18 hours. 1 N NaOH was added and the organic phase was dried (MgSθ4), filtered, and concentrated in vacuo to give the amine 2 as a light yellow oil (9.07 g, 55%). lH NMR (in CDCI3): δ 5.62 (br m,lH,NH-CO), 3.18 (m,2H,N- CH2CH2-NCO), 2.98 (m,4H,2N-CH2CH2-NH2), 2.80 (m,4H,2N- CH2CH2-NH2), 2.57 (m,2H,N-CH2CH2-NHCO), 2.57 (m,4H,2NH2), 1.44 (s,9H,3CH3-C-0) ppm. MS (m z,CI): 247 (100, MH+). IR (CDCI3): 3280, 2965,2815, 1695, 1500, 1165,905,730cπrl.

N,N"-Bis[2-((4-methoxybenzyl)thio)-2-methyl-propionyl]-N' -[2-(N-tert- butoxycarbonyl)aminoethyl]-diethylenetriamine (23)

A solution of the ^l Boc derivative 22 (555.3 mg, 2.25 mmol) in CH2CI2 (25 mL) was cooled to 0°C while 2-[(p-methoxy-benzyl)thio]- 2-methylpropionic acid chloride 19 (1.54 g, 6.85 mmol, prepared according to reference 5) in dichloromethane (10 mL) was added over 5 minutes. The resulting solution was allowed to warm to room temperature and stirred for 12 hours. The solvent was removed in vacuo, I N NaOH was added, and the product was extracted with CH2CI2. The organic layer was washed with water, dried (MgSθ4), filtered, and concentrated in vacuo to give a yellow oil. Rash chromatography of this oil using 5% MeOH/CH2θ2 gave the Φoc derivative 22. as a yellow oil (938 mg, 60.2% yield).

lHNMR(inCDCI3): δ7.16(d,j=8.5Hz,4H,2H3&H5-Ar-OCH3), 7.07 (t,j=5.2Hz,2H,2NH-CO),6.81 (d,j=8.5 Hz,4H,2H2&H6-Ar-OCH3),4.98 (brs,lH,NH-CO),3.77 (s,6H,2CH3θ), 3.63 (s,4H,2S-CH2-Ar), 3.17 (m,6H,3N-CH2CH2-NHCO),2.56(m,6H,3N-CH2CH2-NHCO), 1.53 (s,12H,4CH3-C-S), 1.42 (s,9H,3CH3-C-0)ppm. MS (m/z,CI): 691 (9, MH+). IR(CDCI3): 3380,2970, 2930,2830, 1700, 1650, 1500, 1245, 1170, 1030, 830cm-1.

N,N"-Bis[2-((4-methoxybenzyl)thio)-2-methyl-propionyl]-N' -(2- aminoethyD-diethylenetriamine (24)

A solution of 22 (858.3 mg, 1.24 mmol) in 50% TFA in CH2CI2 (30 mL) was stirred at room temperature for 1 hour. The solvent was removed in vacuo, 1 N NaOH was added, and the product was extracted with CH2CI2. The organic layer was washed with water, dried (MgSθ4), filtered, and concentrated in vacuo to give a yellow oil. Flash chromatography of this oil using 90.5% C/ 9.5% M/ 0.5% H gave the amine 24 as a yellow oil (734 mg, 95.1% yield). lH NMR (in CDCI3): δ 7.25 (m,2H,2NH-CO), 7.16 (d,j=8.5 Hz,4H,2H3&H5-Ar-OCH3), 6.81 (d,j=8.5 Hz,4H,2H2&H6-Ar-OCH3), 3.77 (s,6H,2CH3θ), 3.69 (s,4H,2S-CH2-Ar), 3.23 (q,j=6.1 Hz,4H,2N- CH2CH2-NHCO), 2.72 (t,j=5.9 Hz,2H,N-CH2CH2-NH2), 2.54 (m,6H,N-CH2CH2-NH2 + 2N-CH2CH2-NH-CO), 1.60 (br s,2H,NH2), 1.52 (s,12H,4CH3-C-S) ppm. 13c NMR (in CDCI3): δ 174.3 (s,2NH- CO), 158.3 (s,2Cl-Ar-OCH3), 129.6 (d,2C2&C6-Ar-OCH3), 128.9 (s,2C4-Ar-OCH3), 113.6 (d,2C3&C5-Ar-OCH3), 54.8 (q,2CH3θ), 54.2 (t,N-CH2CH2-NH2), 53.6 (t,2N-CH2CH2-NHCO), 49.4 (s,2S-C-CH3), 38.5 (t,2N-CH2CH2-NHCO), 37.6 (t,N-CH2CH2-NH2), 33.6 (t,2S-CH2- Ar), 26.4 (q,4CH3-C-S) ppm. MS (m/z,CI): 591(31, MH+). IR (CDCI3): 3770, 2930, 2830, 1655, 1510, 1245, 1170, 1030, 830 cm"l.

N,N"-Bis[2-((4-memoxybenzyl)thio)-2-methyl-propionyl]-N'- (2- isothiocvanoethvD-diethylenetriamine (25 )

To a round bottom flask containing the aniline 24 (28.8 mg, 0.0487 mmol) and dichloromethane (10 mL) was added 0.2211 M

solution of thiophosgene (0.22 mL, 0.0509 mmol) in dichloromethane. The heterogeneous reaction mixture was stirred at room temperature for 1 hour and the solvent was removed in vacuo. Flash chromatography of this crude product using 100% EtOAc gave the isothiocyanate __, as a clear oil (18.9 mg, 61.3% yield). lH NMR (in CDCI3): δ 7.17 (d,j ^* =8.5 Hz,4H,2H3&H5-Ar-OCH3), 7.07 (m,2H,2NH-CO), 6.82 (d,j=8.5 Hz,4H,2H2&H6-Ar-OCH3), 3.78 (s,6H, 2CH3O), 3.70 (s,4H,2S-CH2-Ar), 3.49 (t,j=5.9 Hz,2H,N-CH2CH2- NCS), 3.21 (q,j=6.2 Hz,4H,2N-CH2CH2-NHCO), 2.78 (t,j=5.9 Hz,2H,N- CH2CH2-NCS), 2.58 (t,j=6.4 Hz,4H, 2N-CH2CH2-NHCO), 1.54 (s,12H,4CH3-C-S) ppm. MS (m/z,CI): 633(25, MH+). IR (CDCI3): 3370, 2950, 2920, 2850, 2100, 1720, 1655, 1610, 1510, 1245, 1170, 1030, 830 cm-1.

N,N"-Bis[2-((4-methoxybenzyl)thio)-2-methyl-propionyl]-N' -(2-[[[4- memoxyphenyl)amino]mioxomemyl]aminoemyl]-diemylenetriamine

(26)

A solution of the isothiocyanate 2^ (18.9 mg, 0.02986 mmol), triethylamine (7.26 mg, 0.07175 mmol), anisidine (6.9 mg, 0.05602 mmol), and CHCI3 (15 mL) was refluxed for 3 hours and the solvent was removed in vacuo. Flash chromatography of this crude product using 100% EtOAc gave the anisidine derivative 26 as a clear oil (19.8 mg, 87.6% yield). iH NMR (in CDCI3): δ 8.17 (brs,lH,NH-CS-NH-Ar), 7.28 (d,j=8.8 Hz,2H,H2&H6-Ar-N), 7.15 (d,j=8.6 Hz,4H,2H3&H5-Ar-OCH3), 7.06 (brs,lH,NH-CS-NH-Ar), 7.06 (t,j=5.7 Hz,2H,2NH-CO), 6.90 (d,j=8.9 Hz,2H,H3&H5-Ar-N), 6.82 (d,j=8.6 Hz,4H,2H2&H6-Ar-OCH3), 3.79 (s,3H,CH3θ-Ar-N), 3.77 (s,6H,2CH3θ-Ar-CH2), 3.67 (s,4H,2S-CH2- Ar), 3.61 (q,j=5.3 Hz,2H,N-CH2CH2-NHCS), 3.14 (q,j=6.2 Hz,4H,2N- CH2CH2-NHCO), 2.69 (t,j=5.6 Hz,2H,N-CH2CH2-NHCS), 2.52

(t,j=6.3Hz,4H 2N-CH2CH2-NH-CO), 1.51 (br s,12H,4CH3-C-S) ppm. 13C NMR (in CDCI3): δ 181.9 (s,N-CS-N), 175.2 (s,2NH-CO), 158.8 (s,3Cl-Ar-OCH3), 130.0 (s,Cl-Ar-N), 130.0 (d,2C2&C6-Ar-OCH3), 129.2 (s,2C4-Ar-OCH3), 127.0 (d,C2&C6-Ar-N), 114.5 (d,C3&C5-Ar-

N), 114.2 (d,2C3&C5-Ar-OCH3), 55.4 (q,3CH3θ), 54.4 (t,2N-CH2CH2- NHCO), 52.9 (t,N-CH2CH2-NHCS), 50.1 (s,2S-C-CH3), 42.8 (t,N- CH2CH2-NHCS), 38.3 (t,2N-CH2CH2-NHCO), 34.2 (t,2S-CH2-Ar), 28.3 (q,4CH3-C-S) ppm. MS (m/z,FAB): 756(4.2, M+). IR (CDCI3): 3320, 2960, 1720, 1655, 1510, 1290, 1245, 1030 cπrl.

Part 4: Labeling of an N3S2 Chelate

Synthesis of acvclic dimercapto-N.N.N-tris(2-aminoethyl)amine

Preparation of N,N-dimethyl-2-(3 ,3,5 ,11,13,13-hexamethyl- 1 ,2-dithia- 5.8.1 l-triaza-cvclotridecan-8-yl) ethylamine (27)6

To 2-(3,3,13,13-tetramethyl-l,2-dithia-5,8,l 1-triaza- cyclotridecan-8-yl) ethylamine 4 (202.6 mg, 0.63 mmol), in a 25 mL round bottom flask, concentrated formic acid (4 mL) and 37% formaldehyde solution (3.7 mL) was added. The mixture was heated under reflux and stirred for 25 hours. The solution was then cooled to room temperature and extracted three times with ether (50 mL). The aqueous phase was rendered basic (-10-11) by adding 27% ammonium hydroxide and extracted with methylene chloride (4 x 50 mL). The organic phase was washed successively with water (50 mL) and saturated sodium chloride solution (2 x 50 mL), dried with anhydrous magnesium sulfate, and filtered. The solvent was removed under vacuum to give 176 mg (74%) of tetramethylated tetraamine disulfide 22 as a yellow oil. The crude product was purified by flash chromatography (silica gel) using a mixture of methylene chloride, methanol, and ammonium hydroxide (84.5/15/0.5) as eluent. Pure N/V-dimethyl-2-(3,3,5,l 1,13,13- hexamethyl-l,2-dithia-5,8,l l-triaza-cyclotridecan-8-yl) ethylamine 27 (108 mg) was recovered from the purification process.

NτV-dimethyl-2-(3,3,5, 11 , 13, 13-hexamethyl- 1 ,2-dithia-5,8, 11 -triaza- cyclotridecan-8-yl) ethylamine 27 lH NMR (300MHz,in CDCI3): δ 2.71 (t,J=6Hz,4H,-N-CH2-CH2- N(CH3)-), 2.64 (s,4H,-N-CH2-C(CH3)2-S-), 2.62 (t,J=6Hz,4H,-N-CH2-

CH2-N(CH3)-), 2.52 (m,2H,-CH2-CH2-N(CH3)2), 2.46 (m,2H,-CH2- CH2-N(CH3)2), 2.37 (s,6H,-CH2-N(CH3)-CH2-), 2.25 (s,6H,-CH2- CH2-N(CH3)2) and 1.28 (s,12H,-S-C(CH3)2-) ppm. 13c NMR (75MHz,in CDCI3): δ 74.8, 67.7, 57.6, 57.2, 53.9, 51.7, 51.3, 45.9, 45.1 and 26.9 ppm. MS (El; m/z): 376(4,M+), 377(2,M++1), 378(0.6,M++2), 318(1,M+-((CH3)2N-CH2 ^# )). 262 (3), 255 (1), 246(1), 187(7), 156(9), 144(8), 133(9), 130(16), 113 (17), 101(27), 99(21), 98(12), 72(32), 71(28), 70(42), 58(100), 56(13), 55(13), 43(31), and 42(38).

Reduction of 7V,_V-dimethyl-2-(3,3,5,l l,13,13-hexamethyl-l,2-dithia- 5.8.1 l-triaza-cvclotridecan-8-yl) ethylamine (27)"

In a 50 mL three-necked flask equipped with a gas inlet device, a magnetic stirring bar, a stopper and a dry ice condenser 18.9 mg (0.5 μmol) of the tetramethylated tetraamine disulfide (27) was introduced. The condenser was filled with acetone and dry ice, and the contents of the flask was cooled with a dry ice bath. Liquid ammonia was then introduced in the flask until about 25 mL was added. The solution was stirred for several minutes and 36 mg (1.6 mmol) of sodium was added. The mixture was stirred for thirty minutes, and ammonium chloride (172 mg) was cautiously added. The cooling bath was then removed to allow the ammonia to evaporate. The white residue was dissolved with 45 mL of Milli-Q water and concentrated hydrochloric acid was added to brougth the pH of this solution to 1. The mixture was extracted with ether (3 x 50 mL) and the pH was raised to about 9 with 37% ammonium hydroxide. The basic solution was extracted four times with ether (50 mL). The organic phases were combined, washed successively with water (1 x 30 mL) and brine (2 x 30 mL). The ethereal phase was dried with anhydrous magnesium sulfate and filtered. The solvent was then removed under reduced pressure to yield 16 mg of a yellow oil. This oil was used as it is to perform the 99mt _e chnetium labeling study.

Note: The HPLC analysis of this oil has shown that it is a mixture of two component in a ratio of 2.5/1 : the starting material and the reduced compound. The HPLC conditions used for analysis were as followed: column Hamilton PRP-I 10 μm analytical, gradient of 10 to 50% of acetonitrile (with 0.1%

TFA) in 40 minutes. Retention times: tetramethyl tetraamine disulfide= 7.73 min; tetramethyl tetraamine dithiol= 21.55 min.

99mj _{ecnnet m} labeling of a mixture obtained from the reduction of N/V-dimethyl-2-(3,3,5,l 1 , 13, 13-hexamethyl- 1 ,2-dithia-5,8, 11 -triaza- cyclotridecan-8-yl) ethylamine

Experiment A:

In a 1.5 mL plastic conical vial 30 μL of a methanolic solution (~2 μg/μL) of the mixture obtained from the reduction of N,N- dimethyl-2-(3,3,5,l l,13,13-hexamethyl-l,2-dithia-5,8,l 1-triaza- cyclotridecan-8-yl) ethylamine, 0.1 mL Tc-m99 tectnetium glucoheptonate (prepared by the reconstitution of a vial from a FROSST/MAGE GLUCOHEPTONATE kit with 1 mL of sodium Tc-m99 pertechnetate) were introduced. This solution was stirred for 20 seconds with a vortex mixer and heated at 63 °C for 2 1/2 hours. The mixture was then analyzed by ITLC® (Instant Thin Layer Chromatography) ran in acetone and in normal saline and demonstrated that 90% of the radioactivity was tagged with the chelate. HPLC analysis § of the labeling mixture showed the presence of three radioactive products. The first radioactive compound was identified as "" ^m technetium glucoheptonate (Rτ:2.59 min; 19%) while the two others are 99m j _c _ N3S2 chelated species (Rτ:20.72 and 23.08 min; 68 and 8% respectively).

Experiment B:

In a 1.5 mL plastic conical vial 30 μL of a methanolic solution (~2 μg/μL) of the mixture obtained from the reduction of N,N- dimethyl-2-(3,3,5,l l,13,13-hexamethyl-l,2-dithia-5,8,l 1-triaza-

cyclotridecan-8-yl) ethylamine, 0.2 mL Tc-m99 technetium glucoheptonate (prepared by the reconstitution of a vial from a FROSSTIMAGE GLUCOHEPTONATE kit with 1 mL of sodium Tc-m99 pertechnetate) were introduced. This solution was stirred for 20 seconds with a vortex mixer and heated at 65 °C for 1 hour. The mixture was then analyzed by ITLCΛ (Instant Thin Layer Chromatography) ran in acetone and in normal saline and demonstrated that 85% of the radioactivity was tagged with the chelate. HPLC analysis** of the labeling mixture showed the presence of three radioactive products. The first radioactive compound was identified as Tc-m99 technetium glucoheptonate (Rτ.2.72 min; 30%) while the two others are Tc-m99-N3S2 chelated species (RT:20.70 and 23.08 min; 56 and 8% respectively).

% Gelman SG chromatography paper.

§: The high performance liquid chromatography analysis was performed with a Waters 625LC instrument equipped with a Hamilton PRP-I 10 μm analytical column using a 10 to 50% acetonitrile (+TFA) gradient in 40 minutes and a flow rate of 1 mL/min.

1. W.C. Still, M. Kahn, and A. Mitra, J. Org. Chem., __ _. , 2923- 2925 (1978).

2. a) J.J. D'Amico and W.E. Dahl, J. Org. Chem., 4_, 1224-1227 (1975) b) K. Masao, T. Ueno, K. Kojima and Y. Morimoto, (Nippon Shokubai Kagaku Kogyo Co., Ltd.) Jpn. Kokai Tokkyo Koho JP 63,222,155 [88,222,155].

3. E.A. Bayer, B. Haya and M. Wilchek, Biochem. and Biophys. Res. Commun., ___., 872-879 (1986).

4. M.R.A. Pillai, J.M. Lo, C.S. John and D.E. Troutner, Nucl. Med. Biol, IS, 791 (1992).

5. Y. Ohmomo, L. Francesconi, M.P. Kung and H.F. Kung, J. Med. Chem., 21, 157 (1992).

6. M. Apparu, S. DrouiUard, J.P. Mathieu, A. DuMoulinet

D'Hardemare, R. Pasqualini, and M. Vidal, Appl. Radiat. hot., 43 (5), 585-596 (1992).