Field of the Invention The invention generally relates to methods for treating fungal infections.

Background of the Invention The incidence of fungal infections in the immunocompromised population has significantly increased over the past severa ! years, in particular, Candida species, especially Candida albicans, are often significant pathogens in patients infected with human immunodeficinecy virus (HIV). As an example, infections can range from somewhat mild oropharyngeal or vulvovaginal candidiasis to severe debilitating mucocutaneous candidiasis.

Moreover, AIDS patients suffering from oral candidiasis may also experience esophageal candidiasis which has been known to lead to gastrointestinal bleeding and perforation. Candida albicans is a species which is commonly isolated from patients with the above-mentioned infections.

Treatment of candidiasis has typically involved two classes of drugs: (1) polyenes such as amphotericin B and nystatin; and (2) azoles such as clotrimazole, ketoconozole, fluconozole, and itraconazole. Since

immunosuppression in AIDS-infected patients often occurs over an extended period of time, fungal reinfection may be common. Accordingly, these patients commonly receive prolonge antifungal therapy. Widespread antifungal therapy, however, has raised issues regarding the increased level of resistance among isolates of the Candida species, especially with respect to fluconozole. See Pfaller, M. A., et al., Joumal of Clinical Microbiology, Jan 1994, pp. 59-64; and Cameron, M. L., et al., AntimicrobialAgents and Chemotherapy, Nov. 1993, pp. 2449-2453.

In view of the above, there remains a need in the art to develop new antifungal treatment methods utilizing compounds which address the problems noted above. It would especially be desirable if the use of such compounds displayed increased fungal activity at acceptable dosage ievels.

Accordingly, it is an object of the present invention to provide new antifungal treatment methods exhibiting increased fungal activity at acceptable dosage levels.

Summary of the Invention The above object as well as others is provided by the present invention.

In one aspect, the invention provides a method of combating a fungal infection in a subject in need of such a treatment. The method comprises administering to the subject an effective fungal infection-combating amount of a compound (I)-(VI) selected from the group consisting of: wherein R, and R2 may be the same or different and selected from the group consisting of H, loweralkyl, aryl, alkylaryl, aminoalkyl, aminoaryl, halogen, oxyalkyl, oxyaryl, and oxyarylalkyl; and

wherein Y5 and Y6 are present in the meta or para positions and may the same or different and are represented by the formula (a) or (b) selected from the group consisting of: wherein: each R22 is independently selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, cycloalkyl, aryl, or alkylaryl or two R22 groups together represent C2-C10 alkyl, hydroxyalkyl, or alkylene; and R23 is H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; and wherein Y3 is selected from the group consisting of NR"'and O; wherein R"'is selected from the group consisting of H and loweralkyl; and wherein Y4 is represented by the formula: wherein R20 is selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, cycloalkyl, aryl, or alkylaryl; wherein R2, is selected from the group consisting of hydroxy, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, and alkylaryl;

wherein Y s and Y, 6 may be the same or different and represented by the formula: wherein: each R22 is independently selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, alkylamino, cycloalkyl, aryi, or alkylaryl or two R22 groups together represent C2-C, 0 aikyl, hydroxyalkyl, or alkylene; and R23 is H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; wherein each R2s is independently selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, cycloalkyl,

aryl, or alkylaryl or two R25groups together represent substituted or unsubstituted C2-C10 alkyl, hydroxyalkyl, or alkylene; and R26 is H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; R"is hydroxy, alkoxyalkyl, hydroxyalkyl, alkoxyaryl, aryl, or the substituent selected from the formula (i) and (ii) consisting of: wherein: n and m may be independently selected and each range from 0 to 6; each R22 is independently selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, cycloalkyl, aryl, or alkylaryl or two R22 groups together represent C2-C10 alkyl, hydroxyalkyl, or alkylene; and R23 is H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl;

wherein: n is from 2 to 6; X is selected from the group consisting of O, NH, and S; Yg and Y, o may be in the meta or para position, are independently selected and are each represented by the formula: wherein each Rgo is selected from the group consisting of H, hydroxy, loweralkyl, oxyalkyl, alkoxyalkyl, cycloalkyl, aryl, hydroxyalkyl, aminoalkyl, and alkylaminoalkyl; and wherein each of the two R30 groups together may represent C2-C, 0 alkyl, hydroxyalkyl, or alkylene; wherein R3, is selected from the group consisting of H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; wherein R3 and R4 may be the same or different and are selected from the group consisting of H, amino nitro, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, cycloalkyl, aryl, or alkylaryl; wherein X may be O, NH, or S; n and m may be the same or different and range from 2 to 6; wherein Yl, andyl2may be the same or different and represented by the formula:

wherein each R30 is selected from the group consisting of H, loweralkyl, oxyalkyl, alkoxyalkyl, cycloalkyl, aryl, hydroxyalkyl, aminoalkyl, and alkylaminoalkyl; and wherein each of the two R30 groups together may represent represent C2-C, o alkyl, hydroxyalkyl, or alkylene; wherein R3, is selected from the group consisting of H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; wherein Rs is selected from the group consisting of H, hydroxy, and

wherein n ranges from 0 to 3;

wherein X is C, to C, 2 linear or branched, saturated or unsaturated alkyl containing up to four double bonds, or is substituted or unsubstituted aryl; wherein Y, 3 and Y, 4 may be the same or different and are represented by the formula:

wherein R40 and R42are each independently selected from the group consisting of H, loweralkyl, cycloalkyl, substituted aryl, and unsubstituted aryl, or wherein R40 and R42 together may represent represent C2-C, 0 alkyl, hydroxyalkyl, alkylene, substituted aryl, or unsubstituted aryl; and wherein R4, may be H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl.

In yet another aspect, the invention provides compounds for administering to a subject in need of fungal treatment. The compounds are represented by the formula: wherein Yrs and Y, 6 may be the same or different and represented by the formula: wherein: each R22 is independently selected from the group consisting of H, loweralkyl, alkoxyalkyl, hydroxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, aryl, or alkylaryl or two R22groups together represent C2-C, 0 alkyl, hydroxyalkyl, or alkylene; R23 is H, hydroxy, loweralkyl, alkoxyalkyl, aminoalkyl, alkylamino, alkylaminoalkyl, cycloalkyl, hydroxycycloalkyl, alkoxycycloalkyl, aryl, or alkylaryl; and pharmaceutically acceptable salts thereof.

Further, the invention provides the above mentioned compounds and salts thereof as pharmaceutical formulations as described in greater detail herein.

The fungal infections that are addressed by the methods of the invention are generally selected from the group consisting of Candida albicans, Cryptococcus neoformans, Aspergillus fumigatus, Fusarium solani, and combinations thereof. Also, the methods of the invention may be used in combating Candida species other than C. albicans as well as fluconazole- resistant strains of Candida albicans and Cryptococcus neoformans.

The foregoing and other objects and aspects of the present invention are described in greater detail in the specification set forth hereinbelow.

Detailed Description of the Preferred Embodiments The present invention now will be described more fully hereinafter with reference to the accompanying specification and examples, in which preferred embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.

As used herein, the term"lower alkyl"refers to C1 to C4 linear or branched alkyl, such as methyl, ethyl, propyl, butyl, isopropyl, sec-butyl, and tert-butyl. The term"cycloalkyl"as used herein refers to C3 to C6 cyclic alkyl, such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. The term"aryl" as used herein refers to C3 to C10 cyclic aromatic groups such as phenyl, naphthyl, and the like, and includes substituted aryl groups such as tolyl. The term"hydroxyalkyl"as used herein refers to C1 to C4 linear or branched hydroxy-substituted alkyl, i. e.,-CH2OH,- (CH2) 2OH, etc. The term"aminoalkyl" as used herein refers to C1 to C4 linear or branched amino-substituted alkyl, wherein the term"amino"refers to the group NR'R", wherein R'and R"are independently selected from H or lower alkyl as defined above, i. e.,-NH2,- NHCH3,-N (CH3) 2, etc. The term"oxyalkyl"as used herein refers to C1 to C4

oxygen-substituted alkyl, i. e.,-OCH3, and the term"oxyaryl"as used herein refers to C3 to C10 oxygen-substituted cyclic aromatic groups. The term "lower alkoxy"as used herein refers to C1 to C4 linear or branched alkoxy, such as methoxy, ethoxy, propyloxy, butyloxy, isopropyloxy, and t-butyloxy. It should be appreciated that the various groups referred to above may be substituted or unsubstituted with various functional groups known to one skilled in the art.

As noted above, the methods of the present invention are useful for treating antifungal infections attributable to, for example, Candida albicans, Cryptococcus neoformans, Aspergillus fumigatus, Fusarium solani, and combinations thereof. The methods of the invention are useful for treating these conditions in that they inhibit the onset, growth, or spread of the condition, cause regression of the condition, cure the condition, or otherwise improve the general well-being of a subject inflicted with, or at risk of contracting the condition.

Subjects to be treated by the methods of the present invention are typically human subjects, although the methods of the present invention may be useful with any suitable subject known to those skilled in the art.

As noted above, the present invention provides pharmaceutical formulations comprising the aforementioned active compounds, or pharmaceutically acceptable salts thereof, in pharmaceutically acceptable carriers for oral, intravenous, or aerosol administration as discussed in greater detail below. Also, the present invention provides such compounds or salts thereof which have been lyophilized and which may be reconstituted to form pharmaceutically acceptable formulations for administration, as by intravenous or intramuscular injection.

The therapeutically effective dosage of any specific compound, the use of which is in the scope of present invention, will vary somewhat from compound to compound, patient to patient, and will depend upon the condition of the patient and the route of delivery. As a general proposition, a dosage from about 0.1 to about 50 mg/kg will have therapeutic efficacy, with all weights being calculated based upon the weight of the active based,

including the cases where a salt is employed. Toxicity concerns at the higher level may restrict intravenous dosages to a lower level such as up to about 10 mg/kg, with all weights being calculated based upon the weight of the active base, including the cases where a salt is employed.. A dosage from about 10 mg/kg to about 50 mg/kg may be employed for oral administration. Typically, a dosage from about 0.5 mg/kg to 5 mg/kg may be employed for intravenous or intramuscular injection. The duration of the treatment is usually once per day for a period of two to three weeks or until the fungal infection is essentially controlled. Lower doses given less frequently can be used to prevent or reduce the incidence of recurrence of the infection.

In accordance with the present method, pharmaceutically active compounds as described herein, or pharmaceutically acceptable salts thereof, may be administered orally as a solid or as a liquid, or may be administered intramuscularly or intravenously as a solution, suspension, or mulsion. Alternatively, the compounds or salts may also be administered by inhalation, intravenously or intramuscularly as a liposomal suspension. When administered through inhalation the active compound or salt should be in the form of a plurality of solid particles or droplets having a particle size from about 0.5 to about 5 microns, preferably from about 1 to about 2 microns.

The present invention also provides a pharmaceutical composition suitable for intravenous or intramuscular injection. The pharmaceutical composition comprises a compound of Formulas (I) through (VI) described herein, or a pharmaceutically acceptable salt thereof, in any pharmaceutically acceptable carrier. If a solution is desired, water is the carrier of choice with respect to water-soluble compounds or salts. With respect to the water- insoluble compounds or salts, an organic vehicle, such as glycerol, propylene glycol, polyethylene glycol, or mixtures thereof, may be suitable. In the latter instance, the organic vehicle may contain a substantial amount of water. The solution in either instance may then be sterilized in any suitable manner, typically by filtration through a 0.22 micron filter. Subsequent to sterilization, the solution may be filled into appropriate receptacles, such as depyrogenated glass vials. Of course, the filling should be done by an

aseptic method. Sterilized closures may then be placed on the vials and, if desired, the vial contents may be lyophilized.

In addition to compounds of Formula (I) through (VI) or their salts, the pharmaceutical compositions may contain other additives, such as pH- adjusting additives. In particular, useful pH-adjusting agents include acids, such as hydrochloric acid, bases or buffers, such as sodium lactate, sodium acetate, sodium phosphate, sodium citrate, sodium borate, or sodium gluconate. Further, the compositions may contain microbial preservatives.

Useful microbial preservatives include methylparaben, propylparaben, and benzyl alcool. The microbial preservative is typically employed when the formulation is placed in a vial designed for multidose use. Of course, as indicated, the pharmaceutical compositions of the present invention may be lyophilized using techniques well known in the art.

In yet another aspect of the present invention, there is provided an injectable, stable, sterile composition comprising a compound of Formula (I) through (VI), or a salt thereof, in a unit dosage form in a sealed container.

The compound or salt is provided in the form of a lyophilizate which is capable of being reconstituted with a suitable pharmaceutically acceptable carrier to form a liquid composition suitable for injection thereof into a subject.

The unit dosage form typically comprises from about 10 mg to about 10 grams of the compound or salt. When the compound or salt is substantially water-insoluble, a sufficient amount of emulsifying agent which is physiologically acceptable may be employed in sufficient quantity to emulsify the compound or salt in an aqueous carrier. One such useful emulsifying agent is phosphatidyl choline.

Other pharmaceutical compositions may be prepared from the water- insoluble compounds disclosed herein, or salts thereof, such as aqueous base mulsions. In such an instance, the composition will contain a sufficient amount of pharmaceutically acceptable emulsifying agent to emulsify the desired amount of the compound or salt thereof. Particularly useful emulsifying agents include phosphatidyl cholines, and lecithin.

Further, the present invention provides liposomal formulations of the

compounds disclosed herein and salts thereof. The technology for forming liposomal suspensions is well known in the art. When the compound or salt thereof is an aqueous-soluble salt, using conventional liposome technology, the same may be incorporated into lipid vesicles. In such an instance, due to the water solubility of the compound or salt, the compound or salt will be substantially entrained within the hydrophilic center or core of the liposomes.

The lipid layer employed may be of any conventional composition and may either contain cholesterol or may be cholesterol-free. When the compound or salt of interest is water-insoluble, again employing conventional liposome formation technology, the salt may be substantially entrained within the hydrophobic lipid bilayer which forms the structure of the liposome. In either instance, the liposomes which are produced may be reduced in size, as through the use of standard sonication and homogenization techniques.

Of course, the liposomal formulations containing the compounds disclosed herein or salts thereof, may be lyophilized to produce a lyophilizate which may be reconstituted with a pharmaceutically acceptable carrier, such as water, to regenerate a liposomal suspension.

Pharmaceutical formulations are also provided which are suitable for administration as an aerosol, by inhalation. These formulations comprise a solution or suspension of a desired compound described herein or a salt thereof, or a plurality of solid particles of the compound or salt. The desired formulation may be placed in a small chamber and nebulized. Nebulization may be accomplished by compressed air or by ultrasonic energy to form a plurality of liquid droplets or solid particles comprising the compounds or salts.

The liquid droplets or solid particles should have a particle size in the range of about 0.5 to about 10 microns, more preferably from about 0.5 to about 5 microns. The solid particles can be obtained by processing the solid compound or a salt thereof, in any appropriate manner known in the art, such as by micronization. Most preferably, the size of the solid particles or droplets will be from about 1 to about 2 microns. In this respect, commercial nebulizers are available to achieve this purpose. The compounds may be administered via an aerosol suspension of respirable particles in a manner

set forth in U. S. Patent No. 5,628,984, the disclosure of which is incorporated herein by reference in its entirety.

Preferably, when the pharmaceutical formulation suitable for administration as an aerosol is in the form of a liquid, the formulation will comprise a water-soluble compound or a salt thereof, in a carrier which comprises water. A surfactant may be present which lowers the surface tension of the formulation sufficiently to result in the formation of droplets within the desired size range when subjected to nebulization.

As indicated, the present invention provides both water-soluble and water-insoluble compounds and salts thereof. As used in the present specification, the term"water-soluble"is meant to define any composition which is soluble in water in an amount of about 50 mg/mL, or greater. Also, as used in the present specification, the term"water-insoluble"is meant to define any composition which has solubility in water of less than about 20 mg/mL. For certain applications, water soluble compounds or salts may be desirable whereas for other applications water-insoluble compounds or salts likewise may be desirable.

Examples of compounds for use in the methods of the invention include, but are not limited to: 4- (N-cyclopentylamidino)-1, 2-phenylene diamine hydrochloride 2,5-Bis 2- (5-amidino) benzimidazoyl furan hydrochloride 2,5-Bis 2- {5- (2-imidazolino)} benzimidazoyl furan hydrochloride 2,5-Bis 2- (5-N-isopropylamidino) benzimidazoyl furan hydrochloride 2,5-Bis2- (5-N-cyclopentylamidino) benzimidazoyl furan hydrochloride 2,5-Bis2- (5-amidino) benzimidazoyl pyrrole hydrochloride 2,5-Bis2- {5- (2-imidazolino)} benzimidazoyl pyrrole hydrochloride 2,5-Bis2- (5-N-isopropylamidino) benzimidazoyl pyrrole hydrochloride 2,5-Bis2- (5-N-cyclopentylamidino) benzimidazoyl pyrrole hydrochloride 1-Methyl-2,5-Bis2- (5-amidino) benzimidazoyl pyrrole hydrochloride 2,5-Bis2-{5-(2-imidazolino)} benzimidazoyl-1-methylpyrrole hydrochloride 2,5-Bis2- (5-N-cyclopentylamidino) benzimidazoyl 1-methylpyrrole

hydrochloride 2,5-Bis 2- (5-N-isopropylamidino) benzimidazoyl thiophene hydrochloride 2,6-Bis[2-{5-(2-imidazolino)}benzimidazoyl]pyridine hydrochloride 2,6-Bis 2- (5-amidino) benzimidazoyl pyridine hydrochloride 4,4'-Bis 2- (5-N-isopropylamidino) benzimidazoyl-1, 2-diphenylethane hydrochloride 4,4'-Bis [2- (5-N-cyctopentylamidino) benzimidazoyl]-2, 5-diphenylfuran hydrochloride 2,5-Bis 2- (5-amidino) benzimidazoyl benzo [b] furan hydrochloride 2,5-Bis 2- (5-N-cyclopentylamidino) benzimidazoyl benzo [b] furan hydrochloride 2,7-Bis 2- (5-N-isopropylamidino) benzimidazoyl fluorene hydrochloride 2,5-Bis- [4- (3- (N-morpholinopropyl) carbamoyl) phenyl] furan dihydrochloride 2,5-Bis 4- (2-N, N-dimethylaminoethylcarbamoyl) phenyl furan dihydrochloride 2,5-Bis [4- (3-N, N-dimethylaminopropylcarbamoyl) phenyl] furan dihydrochloride 2,5-Bis [4- (3-N-methyl-3-N-phenylaminopropylcarbamoyl) phenyl] furan dihydrochloride 2,5-Bis 4- (3-N, N8, N"-trimethylaminopropylcarbamoyl) phenyl furan dihydrochloride 2,5-Bis 3-amidinophenyl furan dihydrochloride 2,5-Bis- [3- (N-isopropylamidino) amidinophenyl] furan dihydrochloride 2,5-Bis [3 (N-(2-dimethylaminoethyl) amidino phenylfuran dihydrochloride As indicated, the compounds used in the present invention may be present as pharmaceutically acceptable salts. Such salts include the gluconate, lactate, acetate, tartarate, citrate, phosphate, borate, nitrate, sulfate, and hydrochloride salts.

The salts of the present invention may be prepared, in general, by reacting two equivalents of the pyrimidine base compound with the desired acid, in solution. After the reaction is complete, the salts are crystallized from solution by the addition of an appropriate amount of solvent in which the salt is insoluble.

Compounds employed in carrying out the methods of the present invention may be prepared in accordance with techniques known to those skilled in the art, particularly in light of the disclosure and examples set forth below. Exemplary techniques for preparing the compounds are set forth in U. S. Patent Nos. 5,602,172; 4,933,347; 5,723,495; 5,428,051; 5,643,935; 5,639,755; 4,963,589; and 5,578,631, the disclosures of which are incorporated by reference herein in their entirety. For example, the compounds described in Formula (I) can be prepared by: (a) cyclodehydrative furanization of 1,4-diketones according to the procedure taught by R. E. Lutz, et al., J. Am. Chem. Soc. 56: 2698 (1934) to form 2,5-bis- (4-bromophenyl) furan; (b) nitriiization of 2,5-bis (4-bromophenyl) furan using copper (I) cyanide to produce the corresponding bis-nitrile 2,5-bis- (4-cyanophenyl) furan; and (c) conversion of the bis-nitrile to the desired bis-dicationic aryl furan used in the invention.

According to a second method, compounds of Formula (I) may be prepared by (a) converting the appropriate bromoacetophenone to the ethyl bromophenyl-oxopropionate using sodium hydride and diethylcarbonate in tetrahydrofuran, (b) converting the ethyl bromophenyl-oxopropionate to the ethyl bis-bromobenzoyl-propionate using bromophenacyl bromide, (c) converting the bis-bromobenzoyl-propionate to the ethyl bis-bromophenyl furan using ethanol and hydrochloric acid, (d) hydrolysis of the ethyl bis- bromophenyl furan to the bis-bromophenyl furan carboxylic acid using potassium hydroxide followed by hydrochloric acid, (e) converting the carboxylic acid to the corresponding bis-nitrile with copper (I) cyanide and heat, and converting the bis-nitrile to the appropriate bis-dicationic aryl furan.

Conversion of the bis-nitrile to the bis-dicationic aryl furan of Formula (I) may be accomplished according to several methods known to those skilled in the art. According to one method, conversion of the bis-nitrile to the bis-dicationic aryl furan is carried out by conversion into intermediate imidate esters using classical Pinner methodology, followed by reaction of these intermediates with ammonia or the appropriate diamine for example, ethylenediamine, 1,3-propanediamine, etc. According to another method, the

bis-nitrile is converted to the bis-dicationic aryl furan by fusion of the bis-nitrile directly with the hydrochloride salt of the appropriate diamine by thermolysis. This technique is particularly useful for the preparation of compounds wherein two R groups together form a cyclic alkyl.

Compounds described by Formulas (IV) and (V) can be prepared, for example, according to the following procedure with reference to Charts 1-111 described in U. S. Patent No. 4,933,347. Such compounds can also be synthesized according to techniques described in U. S. Patent No. 5,723,495.

More specifically, the compounds may be prepared by first synthesizing known bis-nitriles using Allen's procedure for alkylation of phenols. See J. N.

Ashley et al., J. Chem. Soc. 103-116 (1942); C. F. H. Allen et al., Org. Synth.

Coll. III, (1955). The compounds can then be obtained by using variations of the known techniques of Clement and Raether and by using appropriate reagents. See B. Clement and W. Raether, Arzneim. Forsch. 35,1009-1014 (1985).

Examples The invention will now be described in greater detail with reference to the following examples. It should be noted that these examples are for illustrative purposes only, and are not meant to limit the invention.

Compounds used in the methods of the invention were synthesized in the laboratories of the inventors. The synthesis and physical properties for the following compounds have been previously described as follows: Compounds 1-4 & 7-14,16-20 (Tidwell, R. R., J. Med. Chem., 33: pp. 1252-1257 (1990)); Compound 15 (Jones, S. K., et al., Antimicrob. Agents Chemother. 34: pp.

1026-1030 (1990)); Compounds 21-27 (Berger, B. J., et al., J. Pharmacol. Exp.

Therapeut. 256: pp. 883-889 (1991)); Compounds 28,30,32, and 47 (Fairley, T., et al., J. Med. Chem., 36: pp. 1746-1753 (1993); Tidwell, R. R., et al., J.

Med. Chem. 21: pp. 613-623 (1978)); Compounds 29,31,33,34, and 48-50 (Fairley, T., et al., J. Med. Chem., 36: pp. 1746-1753 (1993)). The synthesis of the remaining compounds, 35-46, and 51-57, along with their physical properties are described below.

The compound melting points were recorded using a Thomas Hoover (Uni-Melt) capillary melting point apparatus and were not corrected. Proton ('H) and Carbon ("C) Nuclear Magnetic Resonance (NMR) spectra of the compounds were recorded employing a Varian GX400 spectrometer and chemical shifts (d) are given in ppm relative to tetramethylsilane (TMS).

Coupling constants (J) are reported in Hertz. Mass spectra (MS) were recorded on a VG Instruments 70-SE spectometer (Georgia Institute of Technology, Atlanta, GA). IR spectra were recorded using a Michelson 100 (Bomen, Inc.) instrument. Elemental analysis was obtained from Atlantic Microlab In.

(Norcross, GA) and are with in 0.4 of the theoretical values. All chemicals and solvents were purchased from Aldrich Chemical Co., St. Louis, MO or Fisher Scientific, Pittsburgh, PA.

Example 1 4-(N-cyclopentylamidino)-1, 2-phenylene(N-cyclopentylamidino)-1, 2-phenylene diamine hydrochloride This compound is used as an intermediate in the synthesis of compounds 38,42,45,54, and 56. Distille cyclopentylamine (1.83 g, 0.021 mol) was added to a stirred suspension of the imidate ester hydrochloride (4.91 g, 0.02 mol) formed from 4-cyano-2-nitroaniline under Pinner type conditions in 30 ml of dry ethanol, the mixture was stirred for 12 h at room temperature and for 1 h at 50°C. The solvent was removed under reduced pressure and the residual thick oily mass was triturated with dry ether and dried under vacuum to yield 4.7 g (95%), mp 168-179°C dec.'H NMR (DMSO-d6): 9. 29 (br, 3H), 8.45 (d, 2H, J = 2.4), 803 (s, 2H), 7.77 (dd. 1H, J = 2.4,8.8), 4.20 (quintet, 1H, J = 6.0), 2.04-2.0 (m, 2H), 1.73-1.65 (m, 4H), 1.57-1.49 (m. 2H). 13C NMR (DMSO-d6): 160.4,148. 5,134.1,129.4,127.3,118. 9,114.6,54.1,31.2,23. 5.

The 4- (N-cyclopentylamidino)-2-nitroaniline (5.0g, 0.02 mol) mp 238-240°C dec; used directly without further characterization (5.0 g, 0.02 mol) and 1.0 g of 10% Pd/C in 130 ml of dry methanol was subjected to hydrogenation at 50 psi for approximately 1 h. The catalyst was filtered over Celite, washed with hot methanol and the solvent of the filtrate was removed under reduced pressure, the residue was triturated with dry ether, and the solid was filtered and dried

under vacuum at 45°C 24 h. The yield of light brown hygroscopic solid was 3.91 g (72%); The compound yielded the following physical properties: mp 170-178°C.'H NMR (DMSO-d6): 8.97 (br s, 1 H), 8.82 (br s, 1 H), 8.64 (br s, 1 H), 6.89 (s, 1 H), 6.88 (d, 1 H, J = 8.4), 6.59 (d, 1 H, J = 8.4), 5.40 (br, 2H), 5.0 (br, 2H) 4.17 (m, 2H), 2.10-1.98 (m, 2H), 1.82-1.76 (m, 4H)."C NMR (DMSO-d6): 162.4,140.8,134.0,118.4,115.6,113.0,112.5,53.7,31.3,23.5. MS (FAB) 219 (M++1). Anal. calc. for C12H18N4#HCl#H2O): 52.84; H, 7.76; N, 20.54. Found: C, 53.10; H, 7.77; N, 20.72.

Example 2 2,5-Bis 2- (5-amidino) benzimidazoyl furan hydrochloride (Compound 35).

A solution of furan-2, 5-dicaboxaldehyde (S. Morikawa, (1979)"Synthesis of hydroxymethylfural and 2,5-furandicarboxaldehydes", Noguchi kenkyusho Jiho, 21: pp. 25-33) (0.8 g 2 mmol), 4-amidino-1, 2-phenylene diamino hydrochloride hydrate (0.8 g, 4 mmol) and 1,4-benzoquinone (0.432 g, 4 mmol) in ethanol (40 ml) was heated at reflux for 4 h (under nitrogen) (Bajic, M. et al., Hetero. Com. 1: 225-230 (1995)). The reaction mixture was cooled to room temperature and the dark solid was collecte by filtration, washed with cold ethanol and then anhydrous ether, and dried to yield 0.55 g (71%) of the free base. This solid was dissolve slowly in hot ethanol (300 ml) and filtered. The filtrate volume was reduced to 70 ml and acidified with HCI saturated ethanol.

After standing overnight in the refrigerator, the green solid was collecte by filtration, washed with anhydrous ether and dried under vacuum to yield 0.4 g (52%) yield of solid. The compound demonstrated the following physical properties: mp > 300°C.'H NMR (DMSO-d6): 9.30 (s, 4H); 8.19 (2s, 2H), 7.81, (d, 2H, J = 8.8), 7.72 (d, 2H, J = 8.4). 7.60 (s, 2H)."C NMR (DMSO-d6/D2O): 166.8,146. 4,146.1,142.2,139.7,123.4,122. 7,117.1,116.1,115.4, MS (FAB): m/z 385 (M++1); HRMS: calc. mass (free base) 385.1525 (M++1); observed mass: 385.1535. Anal. calc. for C2oH, 6N8O2HCI-1.5 H20: C, 49.59; H, 4.37; N, 23.14. Found: C, 49.40; H, 4.31; N, 22.96.

Example 3 2,5-Bis [2- {5- (2-imidazolino)} benzimidazoyl] furan hydrochloride (Compound 36).

A procedure similar to that described above was employed for the condensation of 2, 5-furandicarboxaldehyde (S. Morikawa, (1979)"Synthesis of hydroxymethylfural and 2,5-furandicarboxaldehydes", Noguchi kenkyusho Jiho, 21: pp. 25-33) and 2- (3, 4-diaminophenyl) imidazoline (Fairley, T., (1993) J. Med.

Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to give a 38% yield of a green powder. This compound demonstrated the following physical properties: mp <300°C,'H NMR (DMSO-d6): 10.53 (s, 4H), 8.38 (s, 2H), 7.87 (d, 2H, J = 8.5), 7.83 ( d, 2H, J = 8.2), 7.62 (s, 2H), 4.04 ( s, 8H).'3MR (DMSO-d6/D20): 166.3,146.2,146. 1,142.3,139.8,123.7,117.6, 116.9,116.1,115.5,45.0. MS (FAB): m/z 437 (M++1); HRMS: calc. mass (free base): 437.1838 (M++1); observed mass: 437.1832. Anal. calc. for C24H2oN8O. 2HCI. 5H2O: C, 48.08; H, 5.38; N, 18.69. Found: C, 48.22; H, 5.25; N, 18.51.

Example 4 2,5-Bis [2- (5-N-isopropylamidino) benzimidazoyl] furan hydrochloride (Compound 37).

A procedure similar to that described above was employed for the condensation of 2, 5-furandicarboxaldehyde (S. Morikawa, (1979)"Synthesis of hydroxymethylfural and 2,5-furandicarboxaldehydes", Noguchi kenkyusho Jiho, 21: pp. 25-33) and 4- (N-isopropylamidino)-1, 2-phenylene diamine (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to give a 54% yield of a yellow-green powder. This compound displayed the following physical properties: mp > 300°C. ¹H NMR(DMSO-d6): 9.60 (s, 1 H), 9.58 (s, 1 H), 9.45 (s, 2H), 9.04 (s, 2H), 8.06 (s, 2H), 7.82 (d, 2H, J = 8.4), 7.69 ( s, 2H), 7.62 (d, 2H, J = 8.2), 4.09 (m, 2H, J = 7.0), 1.32 (d, 12H, J = 6.3)."C NMR (DMSO-d6/D2O): 162.8,145. 9,145.1,140.9,138.5,124.5, 124.0,116.9,115.9,115.8,45.9,21.7. MS (FAB): m/z 469 (M++1); HRMS: calc.

mass (free base): 469.2464 (M++1); observed mass: 469.2475. Anal. calc. for: C26H28N8O. 3HCI. 2. 5H2O: C, 50.12; H, 5.83; N, 17.99. Found: C, 50.45; H, 5.76; N, 17.64.

Example 5 2,5-Bis 2- (5-N-cyclopentylamidino) benzimidazoyl furan hydrochloride (Compound 38).

A procedure similar to that described above in the previous examples was employed for the condensation of 2, 5-furandicarboxaldehyde and 4- (N- cyclopentylamidino)-1, 2-phenylene diamine to give a 77% yield of a yellow- green powder. The following physical properties were obtained: mp 287-289 °C dec.'H NMR (DMSO-d6'D20): 8.07 (s, 2H), 7.82 (d, 2H, J = 8.4), 7.66 (s, 2H), 7.63 (d, 2H, J = 8.4), 4.22-4.14 (m, 2H), 2.14- 2.04 (m, 4H), 1.82-1.67 (m, 8H), 1.64-1.56 (m, 4H). 13C NMR (DMSO-d6): 163.0,145.4,144.5,140.4,137.7, 123.9,116.4,115.5,115.2,54.6,31.5,23.7. MS (FAB) 521 (M++1). Anal. calc. for C3oH32N804HCI: C, 54.06; H, 5.44; N, 16.81. Found: C, 53.80; H, 5.51; N, 16.68.

Example 6 2,5-Bis 2- (5-amidino) benzimidazoyl pyrrole hydrochloride (Compound 39).

A procedure similar to that described in the above examples was employed for the condensation of 4-amidino-1, 2-phenylene diamino hydrochloride hydrate (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) with pyrrole-2,-5- dicarboxaldehyde (Miller, R., (1981) Acta Chem. Scand., B: 303-304) to yield 0.83 g (76%) of solid. The compound displayed the following physical properties: mp > 300 °C.'H NMR (DMSO-d6): 9.48 (brs, 1H), 9.18 (brs, 1H), 8.25 (s, 2H), 7.87 (d, J = 8.4,2H), 7.80 (dd, J = 8. 8 and 0.8,2H). 7.54 (s, 2H).

MS (free base): m/e 384 (M++1). Anal., calc. for C2oH, 7Ng. 3HCl. 3H2O: C, 43.93; H, 4.73; N, 23.05. Found: C, 43.61; H, 4.62; N, 22.79.

Example 7 2,5-Bis[2-{5-(2-imidazolino)}benzimidazoyl]pyrrole hydrochloride (Compound 40).

A procedure similar to that described in the above examples was used for the condensation of pyrrole-2, 5-dicarboxaldehyde and 2- (3,4- diaminophenyl) imidazoline (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to give a 86% yield of solid.

The compound dispalyed the following physical properties: mp > 300 °C.'H NMR (DMSO-d6): 10.71 (s, 1H), 8.44 (s, 2H), 7.92 (dd, J = 8.4 and 1.6,2H), 7.86 (d, J = 8.8,2H), 7.39 (s, 2H), 4.04 (s, 8H). MS (free base): m/e 436 (M++1).

Anal. calc. for C24H21N9#3HCl#4H2O: 46.72; H, 5.23; N, 20.43. Found: C, 46.49; H, 5.11 ; N, 20.28.

Example 8 2,5-Bis 2- (5-N-isopropylamidino) benzimidazoyl pyrrole hydrochloride (Compound 41).

A procedure similar to that described in the above examples was used for the condensation of pyrrole-2,5-dicarboxaldehyde and 4- (N- isopropylamidino)-1,2-phenylene diamine (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to yield (79%) of a yellow-green solid. The compound displayed the following physical properties: mp 287-289°C NMR (DMSO-ds/D2O): 8.06 (s, 2H), 7.81 (d, 2H, J = 8.4), 7.65 (d, 2H, J = 8.4), 7.41 (s, 2H), 4.06 (septet, 2H, J = 6.4), 1.30 (d, 12H, J = 6.4).'3C NMR (DMSO-d6/D2O): 162.3,145. 8,138.6,135.7,124.7, 124.2,123.9,115. 7,115.5,114.9,45.7,21.4. MS (FAB) 468 (M'+1). Anal. calc. for C26H29Ng. 4HCl: C, 50.90; H, 5.42; N, 20.55. Found: C 51.54; H 5.57; N 20.30.

Example 9 2,5-Bis [2- (5-N-cyclopentylamidino) benzimidazoyl] pyrrole hydrochloride (Compound 42).

A procedure similar to that described in the above examples was employed for the condensation of 4- (N-cyclopentylamidino)-1, 2-phenylene diamine with pyrrole-2,-5-dicarboxaldehyde (Miller, R., (1981) Acta Chem.

Scand., B: 303-304) to yield (71 %) a blue-green solid. The compound displayed the following physical properties: mp 290-294°C.'H NMR (DMSO- d6/D2O): 8.0 (s, 2H), 7.77 (d, 2H, J = 8.4), 7.60 (d, 2H, J = 8.4), 7.32 (s, 2H), 4.09 (br m, 2H), 2.11-1.97 (m, 4H), 1.77-1.62 (m, 8H), 1.61-1.50 (m, 4H).'3C NMR (DMSO-d6/D20): 163.1,145.7,138.6,135.6,124.6,124.3,123.8,115.8, 115.5,115.1,55.0,31.7,23. 9. MS (FAB) m/z 520 (M++1). Anal. calc. for C3oH33Ng. 4HC !. 0. 0. 5 H20: C, 53.42; H, 5.63; N, 18.68. Found: C 53.90; H 5.75; N 18.16.

Example 10 1-Methyl-2, 5-Bis 2- (5-amidino) benzimidazoyl pyrrole hydrochloride (Compound 43).

A procedure similar to that described in the above examples was employed for the condensation of 4-amidino-1, 2-phenylene diamine hydrochioride hydrate (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) with 1-methylpyrrole-2,-5- dicarboxaldehyde (Cresp, T. M., (1973) J. Chem. Soc., Perkin Trans. 1: 2961- 2971) to give a 70 % yield of product. The compound displayed the following physical properties: mp>300°C;'H NMR (DMSO-d6): 9.38 (brs, 1H), 9.11 (br s, 1 H), 8.19 (s, 2H), 7.80 (d, J = 8.4), 7.73 (dd, J = 8 and 1.2,2H), 7.33 (s, 2H), 4.72 (s, 3H). MS (free base): m/z 398 (M++1). Anal. calc. for C2, H,: C, 48.06; H, 4.61; N, 24.02. Found : C, 48.16; H, 4.58; N, 23.93.

Example 11 2,5-Bis 2- 5- (2-imidazolino)} benzimidazoyl-1-methylpyrrole hydrochloride (Compound 44).

A procedure similar to that described in the above examples was employed for the condensation of 2- (3, 4-diaminophenyl) imidazoline (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) with 1-methylpyrrole-2,-5-dicarboxaldehyde. A yield of 83% of solid mp > 300°C was obtained. The following additional physical properties were determined:'H NMR (DMSO-d6): 10.60 (s, 1H), 8.36 (s, 2H), 7.84 (dd, J = 8.4 and 8,4H), 7.30 (s, 2H), 4.72 (s, 3H), 4.04 (s, 8H). MS (free base): m/e 450 (M++1). Anal. calc. for C2sH23Ng. 3HCl. 3H2O: C, 48.98; H, 5.26; N, 20.57.

Found: C, 49.20; H, 4.79; N, 20.51.

Example 12 2,5-Bis 2- (5-N-cyclopentylamidino) benzimidazoyl 1-methylpyrrole hydrochloride (Compound 45).

A procedure similar to that described in the above examples was employed for the condensation of 4- (N-cyclopentylamidino)-1, 2-phenylene diamine with 1-methyl-2,-5-pyrrole dicarboxaldehyde (Cresp, T. M., (1973) J.

Chem. Soc., Perkin Trans. 1: 2961-2971) to yield (85%) a blue solid having a mp of 324-326°C. The following addition physical properties were determined: dec.'H NMR (DMSO-d6/D2O): 8.0 (s, 2H), 7.73 (d, 2H, J = 8.4), 7.55 (d, 2H, J=8. 4), 7.13 (s, 2H), 4.57 (s, 3H), 4.14 (quintet, 2H, J=5. 2), 2.12- 2.02 (m, 4H), 1.80-1.58 (m, 12H). MS (FAB) 534 (M++1). Anal. calc. for C31H35N9#3HCl#H2O, C: 56.32; H, 6.10; N, 19.07. Found: C 56.90; H 5.97; N 18.83.

Example 13 2,5-Bis 2- (5-N-isopropylamidino) benzimidazoyl thiophene hydrochloride (Compound 46).

A procedure similar to that described in the above examples was employed for the condensation of 2, 5-thiophenedicarboxaldehyde and 4- (N- isopropylamidino)-1, 2-phenylene diamine (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to give a 75% yield a green yellow solid 290-292 °C. The physical properties for this compound were determined to be: dec.'H NMR (DMSO-d6/D2O): 8.18 (s, 2H), 8.05 (s, 2H), 7.77 (d, 2H, J = 8.4); 7.60 (d, 2H, J = 8.4), 4.11 (quintet, 2H, J = 6.4), 1.31 (d, 12H, J = 6.4). MS (FAB) m/z 485 (M++1). Anal. calc. for C26H2aN8S. 3HCl. H2O. C, 51.02; H, 5.43; N, 18.31; Cl, 17.38. Found: C 51.56; H 5.54; N 18.09; Cl, 17.37.

Example 14 2,6-Bis[2-{5-(2-imidazolino)}benzimidazoyl]pyridine hydrochloride (Compound 51).

A procedure similar to that described in the above examples was used for the condensation of 2,6-pyridine carboxyaldehyde and 2- (3,4- diaminophenyl) imidazoiine (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to give an 85% yield of solid mp > 300°C. The physical properties for this compound were found to be:'H NMR (DMSO-d6): 10.71 (s, 1 H), 8.51-8.49 (m, 4H), 8.30 (m, 1 H), 7.96 (m, 4H), 4.05 (s, 8H). MS (free base): m/e 448 (M++1). Anal. calc. for C25H21N9#3HCl#3H2O: C, 49.15; H, 4.94; N, 20.63. Found: C, 49.14; H, 4.68; N, 20.51.

Example 15 2,6-Bis[2-(5-amidino)benzimidazoyl]pyridine hydrochloride(Compound 52).

A procedure similar to that described in the above examples was used to condense 2,6-pyridine dicarboxaldehyde with 4-amidino-1,2-phenylene diamine hydrochloride hydrate (Fairley, T., (1993) J. Med. Chem., 36: 1746-1753; Tidwell, R. R., (1978) J. Med. Chem., 21: 613-623) to yield 89% of a solid mp > 300 °C. The physical properties for this compound were determined to be:'H NMR (DMSO-d6): 9.45 (brs, 1H), 9.12 (brs, 1H), 8.51 (d, J = 8,2H), 8.34-8.28 (m, 3H), 7.94 (d, J = 8.4,2H), 7.79 (dd, J = 8.4 and 1.6,2H). MS (free base): m/z 396 (M++1). Anal. calc. for C2, H, 7Ng. 3HCl. 3H2O: C, 45.13; H, 4.69; N, 22.56. Found: C, 45.16; H, 4.58; N, 22.45.

Example 16 4,4'-Bis 2- (5-N-isopropylamidino) benzimidazoyl-1, 2-diphenylethane hydrochloride (Compound 53).

1,2-Bis- (4-cyanophenyl) ethane was prepared in one step from 2,3-bis- (4-bromophenyl) propanoic acid (Dann, O., (1971) LiebigsAnn. Chem., 749: 68- 89) by the action of CuCN in DMF (Das, B. P., et al., J. Med. Chem., 20: 531-536) in a 50% yield; mp 195-197 °C.'H NMR (DMSO-d6): 7.68 (d, 4H, J = 8), 7.40 (d, 4H, J = 8), 3.01 (s, 4H).'3NMR (DMSO-d6): 146.7,131.9,129.3, 118.6,108.6,35.8. MS m/e 232 (M++1). 1,2-Bis- (4-cyanophenyl) ethane was used without further characterization and on treatment with DIBAL gave a white crystalline solid (CHCI3: ether) 76% mp 121-122 °C of 1,2-bis- (4- formylphenyl) ethane.'H NMR (DMSO-d6): 9.96 (s, 2H), 7.80 (d, 4H, J = 8), 7.44 (d, 4H J = 8), 3.05 (s, 4H). 13C NMR (DMSO-d6/D2O): 192.0,184.0,134.2, 129.1,128.8,36. 0. Anal. Calc. for C, 6H, 402@0. 1 H2O: C, 80.04; H, 5.96. Found: C, 80.09; H, 5.98. A protocol similar to that described above was employed for the condensation of 1,2-bis- (4-formylphenyl) ethane and 4- (N-isopropylamidino)- 1,2-phenylene diamine (18,35). A 75% yield of a purple solid mp > 320 °C.'H NMR (DMSO-d6/D2O): 8.09 (d, 4H, J = 8), 8.06 (s, 2H), 7.83 (d, 2H, J = 8.4),

7.65 (d, 2H, J = 8.4), 7.48 (d, 4H, J = 8), 4.03 (br m, 2H), 3.07 (br, 1.29 (d, 12H, J = 6). ¹³NMR(DMSO-d6/D2O): 162.4,153. 0, 146. 6, 138.3, 135. 4, 129.8, 127.9,124.8,124.1,123. 5,115.5,115. 0,45.6,36.2,21.2. MS (FAB) 583 (M++1)Anal. calc. for C36H38N8#4HCl#0.5H2O: C, 58.61; H, 5.87; N, 15.19.

Found: C, 58.31; H, 5.79; N, 15.02.

Example 17 4,4'-Bis 2- (5-N-cyclopentylamidino) benzimidazoyl-2, 5-diphenylfuran hydrochloride (Compound 54).

2,5-Bis (4-formylphenyl) furan was prepared by reduction of 2,5-bis- (4- cyanophenyl) furan (Bajic, M., (1996) Heterocyclic Com. 2: 135-140) (1.12 g 0.004 mol) using 1M DIBAL in CH2Cl2 (1.83g, 0.012 mol) to yield apale yellow solid, 0.77 g (70%), mp 173-4 °C (CHC ! g: ether).'H NMR (DMSO-d6/D2O) 10.0 (s, 2H), 8.05 (d, 4H, J = 7.5), 7.97 (d, 4H, J = 7.5), 7.37 (s, 2H). ¹³C NMR (DMSO-d6/D2O) 192.0,125.7,135. 0,134.6,130.1,123.9,111.6. MS m/e 276.

Anal. calc. for C, 8H, 203: C, 91.49; H, 5.12. Found: C, 91.22; H, 5.38.

A procedure similar to that described in the above examples was employed for the condensation of 4-(N-cyclopentylamidino)-1,2-phenylene diamine with 2,5-bis (4-formylphenyl) furan to yield (77%) of a yellow solid mp 295-297 °C dec.'H NMR (DMSO-d6/D2O): 8.30 (d, 4H, J = 8.4), 8.05 (d, 4H, J = 8.4), 8.01 (s, 1H), 7.77 (d, 2H, J = 8.4), 56 (d, 2H, J = 8.4), 7. 27 (s, 2H), 4.15 (br, 2H), 2.13-2.03 (m, 4H), 1.81-1.55 (m, 12H).'3C NMR (DMSO-d6/D2O): 163.7,154.0,153.1,141.2,138.6,132.8,127.9,126.1,124.6,123. 3,123.1, 115.9, 115. 7, 111. 0, 55. 7, 32. 3, 24. 4. MS (FAB) m/z 673 (M++1). Anal. calc. for C42H4oN8Oo4HCI: C, 61.61; H, 5.42; N, 13.69. Found: C 62.28; H 5.74; N 13.62.

Example 18 2,5-Bis [2-(5-amidino)benzimidazoyl]benzo[b]furan hydrochloride (Compound 55).

A procedure similar to that in the above-described examples was employed for the condensation of benzo b furan-2, 5-dicarboxaldehyde and 4-

amidino-1, 2-phenylene diamine hydrochloride hydrate to give a 70% yield a blue-gray solid mp 338-340°C dec.'H NMR (DMSO-d6/D2O) 8.6 (s, 1H), 8.27 (d, 1 H, J = 8), 8.19 (d, 2H, J = 9.6), 7.89 (d, 1 H, J = 8.8), 7.87 (s, 1H), 7.83 (d, 1 H, J = 8.4), 7.78 (d, 1H, J = 7.73 (d, 1H, J = 7.68 (d, 1 H, J = 8).

'3C NMR (DMSO-d6/D2O) 166.4,165.9,156.6,153.5,147.4,145. 4, 141.6,139.9,139.1,136.9,128.6,126.2,123.3,122.9,122. 6,122.2, 122.1,116.9,115.8,115.5,115. 0,112.8,108.6. MS (FAB) 435 (M++1). Anal. calc. for C24H18N8O#3HCl#H2O: 51.30; H, 4.12; N, 19.94. Found: C, 51.72; H, 4.14; N, 15.64.

Example 19 2,5-Bis [2- (5-N-cyclopentylamidino) benzimidazoyl] benzo b furan hydrochloride (Compound 56) 2-Acetyl-5-bromobenzo [b] furan was prepared as reported in the literature (Dann, O., (1972) Liebigs Ann. Chem., 760: 37-87) in an 86% yield; mp 110-111 °C (lit = 108-111 °C)'H NMR (DMSO-d6): 8.02 (d, 1 H, J = 1.6), 7.79 (s, 1 H), 7.68 (d, 1 H, J = 9.2), 7.65 (dd, 1H, J = 9.2,1.6), 2.58 (s, 3H).'3C NMR(DMSO-d6):(DMSO-d6): 181.6, 153.5, 152.9, 130.9, 128.8, 125.7, 115.9, 114.1, 112.9,26.2. MS m/z The acetyl compound was converted into 5- bromobenzo b furan-2-carboxylic acid in a 77% yield as reported (15) mp 258- 262 °C(lit = 258-262 °C). ¹H NMR (DMSO-d6/D2O): 7.95 (d, 1H, J = 1.6), 7.64 (d, 1 H, J = 8.8), 7.58 (dd, 1 H, J = 8.8,1. 6), 7.57 (s, 1 H).'3C NMR (DMSO- d6/D2O): 159.5,153. 6,147.3,129. 9,128.9,125.2,115.8,113.9,112.5. MS m/z 241 (M+). 5-Bromobenzo [b] furan-2-carboxylic acid, used without further characterization, was converted, using standard procedures via the acid chloride, into 5-bromo-2-carboxamidobenzo [b] furan in a 81 % yield; mp 208- 210 °C.'H NMR (DMSO-d6): 8.2 (brs, 1H), 7.99 (s, 1H), 7.77 (brs, 1H), 7.61 (d, 1 H, J = 8.8), 7.57 (dd, 1 H, J = 8.8,2) 7.51 (s, 1 H).'3C NMR (DMSO-d6/D2O): 159.4,153.0,150.5,129.4,128.3,125.2,115.9,113.9,109.0. MS m/e 240 (M+). The amide, used without further characterization, was dehydrated employing POCI3 to form 5-bromo-2-cyanobenzo [b] furan in a 88% yield mp

147-148 °C.'H NMR (DMSO-d6) 8.0 (s, 1H), 7.97 (s, 1H), 67 (brs, 2H).'3C NMR (DMSO-d6) 153.7,131.1 127.2,127.1,125.2,118.8,116. 7,113.7,111.1.

MS m/e 222 (M+). 5-Bromo-2-cyanobenzo [b] furan, used without further characterization, was converted via a standard procedure (Newman, M. S., (1961) J. Org. Chem., 26: 2525) into 2,5-dicyanobenzo [b] furan in a 79% yield; mp 166-167 °C.'H NMR (DMSO-d6): 8.39 (s, 1H), 8.14 (s, 1H), 7.97(d, 1H, J = 8.8) 7.92 (d, 1H, J = 8.8).'3C NMR (DMSO-d6): 156.3,131.5 128.5,128.2, 125.8,119.3,117.9,113. 4,110.8,107.7. MS m/e 168 (M+). Anal. calc. for ClOH4N20 : C, 71.42; H, 2.39; N, 16.16. Found: C, 71.78; H, 2.46; N, 16.51.2,5- Diformylbenzo [b] furan was prepared by reduction of the bis-nitrile using DIBAL which was added dropwise to a stirred solution of the bis-nitrile (1.68 g, 0.01 mol) in 150 mi dry methylene chloride under nitrogen. The mixture was stirred for 15 min, allowed to reflux for 40 min and the mixture was cooled. 100 ml of 1MH2SO4 was added dropwise while maintaining the solution temperature below 25°C. The methylene chloride layer was separated, the aqueous layer was extracted with 100 ml of methylene chloride, and the combined organic phases were washed with 20% NaHCO3, dried over Na2SO4. The solvent was removed under reduced pressure and the residue was triturated with 1: 1 ether: hexane. The resulting white solid was filtered, dried in a vacuum to yield 1.2 g (69%) mp 141-142 °C. 'H NMR (DMSO-d6): 10.1 (s, 1H), 9.92 (s, 1H), 8.48 (d, 1H, J = 8.10 (s, 1H), 8.08 (dd, 1 H, J = 0.8,8.88), 7.90 (d, 1H, J = 8.8).'3C NMR (DMSO-d6): 191.8,180.6,158.1,153.6,132.9,128.9,127.5, 126.9,118.8,113.1. Anal. calc. for C, oH6N2. 0. 2 H2O: C, 67.75; H, 3.67. Found: C, 67.83; H, 3.59. A protocol similar to that described above was employed for the condensation of 4- (N-cyclopentylamidino)-1, 2-phenylene diamine with benzo [b] furan-2,5-dicarboxaldehyde to yield gray solid in a 73% yield; mp 290-292 °C dec.'H NMR (DMSO-d6/D2O): 8.62 (s, 1 H), 8.27 (d, 1 H, J = 8.8), 8.08 (s, 1H), 8.05 (s, 1H), 7.95 (d, 1H, J = 8.8), 7.90 (s, 1H), 7.84 (d, 1H, J = 8.8), 7.79 (d, 1H, J = 7.64 (d, 1H, J = 7.57 (d, 1H, J = 4.14 (br 2H), 2.13-2.06 (m, 4H), 1.81-1.56 (m, 12H).'3C NMR (DMSO-d6/D2O): 163.4,163.1,156.9, 153.2,147.6,145.2,141.2,138.8,136. 2, 128.9,126.5,124.5,124.1 123. 9,

123.5 122.5, 122.4,116.9, 116.1,115.8,115.7,115.1,113.2,108.8,54.9,54.8, <BR> <BR> <BR> <BR> 31.7,23.9. MS (FAB) m/z 571(M++1).Anal. calc. for C34H34N8O#4HCl: 56.99; H, 5.34; N, 15.64. Found: C, 56.89; H, 5.34; N, 15.53.

Example 20 2,7-Bis [2- (5-N-isopropylamidino) benzimidazoyl] fluorene hydrochloride (Compound 57).

A mixture of 2, 7-dibromofluorene 6.48 g (0.02 mol) and cuprous cyanide 5.37 g (0.06 mol) in 35 ml quinoline was heated under reflux for 2 h (followed by Thin Layer Chromatography, silica gel Kodak), benzene mobile phase). The mixture was cooled and extracted with 2X 150 ml chloroform. organic layer was stirred with 200 ml 2M. HCI for 2 h, washed with water, dried over anhydrous Na2SO4, filtered, dried, concentrated, redissolved in minimum amount of chloroform, chromatographed over neutral alumina. Thecolumn was first eluted with hexane: ether (2: 1) to remove residual quinoline and finally with ether: CHOC'3 (1 : 1) to CHCI3 to afford fluffy pale solid 2.72 g (63%) mp 282-4 °C of 2,7-dicyanofluorene.'H NMR (DMSO-d6/D2O): 8.16 (d, 2H, J = 8.4), 8.04 (s, 2H), 7.83 (d, 2H, J = 8.4), 4.07 (s, 2H).'3C NMR (DMSO-d6/D2O): 144. 2, 143.3,130.8,128.5,121.7,118.5,110.1,36.0. MS m/z 216(M+). Anal. calc. for C, 5H8N2 : C, 83.21; H, 3.72; N, 12.95. Found: C 83.21; H 3.78; N 12.99. To a stirred solution of 2,7- dicyanofluorene (2.16 g, 0.01 mol) in 150 ml of dry CH2CI2 was added DIBAL (1 M in cyclohexane, 4.26 g, 0.03 mol) under nitrogen at room temperature. The suspension was heated at 40 °C for 1 h, cooled, 100 ml 1M H2SO4 was added dropwise and stirred for 1h, the precipitated yellow solid was filtered, recrystallized from CHCI3: ether to yield 2,7- diformylfluorene as pale crystalline solid, mp 218-220 °C, 1.6 g (72%).'H NMR (DMSO-d6/D2O) 10.08 (s, 2H), 8.16 (d, 2H, J = 8.0), 8.11 (s, 2H), 7.95 (d, 2H, J = 8.0), 4.10 (s, 2H).'3C NMR (DMSO-d6/D2O) 191. 9) 145.0,144.7,135.6,128.5,125.4,121.1, 36.0. MS m/e 222 (M+). Anal. calc. for C15H10O2#0.1 C, 80.41; H, 4.49.

Found: C, 80.32; H, 4.63. A procedure similar to that in the above-described examples was used for the condensation of 2, 7-diformylfluorene and 4- (N-

isopropylamidino)-1,2-phenylene diamine to yield (72%) of a green solid mp 310-313 °C dec.'H NMR (DMSO-d6/D2O): 8.53 (s, 2H), 8.34 (d, 2H, J = 8.4), 8.22 (d, 2H, J = 8.4), 8.11 (s, 2H), 7.85 (d, 2H, J = 8.4), 7.65 (d, 2H, J = 8.4), 4.23 (s, 2H), 4.09 (quintet, 2H, J = 6.4), 1.33 (d, 12H, J = 6.4)."C NMR (DMSO-d6/D2O) 162.2,153.1,144.9,143.5,138.7,136. 3,126.9,125.7,124.3, 123.6,121. 7,115.6,114.7,45.3,36.7,21.1. MS m/z (FAB) 567 (M++1). Anal. calc. for C3sH34N2. 4HCI: C, 58.99; H, 5.37; N, 15.73. Found: C, 59.14; H, 5.59; N, 15.43.

Examples 21-25 Compounds described in these examples were synthesized in the laboratories of the inventors. Stock solutions of 10,000 Xug were made in sterile distilled water or dimethyl sulfoxide (DMSO). The solutions were filter sterilized by passage through a 0.22 pm Millex Durapore membrane filter, and stored at-70°C until use. The synthesis and physical properties for the following compounds are set forth in the following references: compounds 1- 15 (Patrick, D. A., et al., Eur. J. Med. Chem., 32: pp. 781-793 (1997)); compounds 16 and 17 (Das, B. P., et al., J. Med. Chem. 20: pp. 531-536 (1977)); compound 18 (Boykin, D. W., et al., Biorg. and Med. Chem. Letters 6: pp. 3017-3020 (1996)); compounds 19 and 25 (Trent, J. O., et al., J. Med.

Chem. 39: pp. 4554-4562 (1996)); compounds 20-24 (Boykin, D. W., et al., J.

Med. Chem., 41: pp. 124-129 (1998)); compounds 48-63 (Czarny, A. W., et al., J. Heterocyclic Chemistry, 33: pp. 1393-1397 (1996)), and compounds 64- 67 (Tidwell, R. R., et al., J. Med. Chem., 21: pp. 613-623 (1978). A brief description of the synthesis and physical properties of the other compounds (33-38, and 40-41) is as follows.

Melting points were recorded using a Thomas Hoover (Uni-Melt) capillary melting point apparatus or a Fischer-Johns apparatus and are uncorrected.'H NMR and 13C NMR spectra were recorded employing a Varian GX400 spectrometer and chemical shifts (6) are in ppm relative to TMS and coupling constants (J) are reported in Hertz. Mass spectra were recorded on a VG Instrument 70-SE spectrometer (Georgia Institute of

Technology, Atlanta, GA). IR spectra were recorded using a Michelson 100 instrument (Bomem, Inc.). Elemental analysis were obtained from Atlanta Microlab Inc. (Norcross, GA) and are within a tolerance of 0.4 of the theoretical values. All chemicals and solvents were Aldrich Chemical Co. or Fisher Scientific.

In Examples 21-25, to a suspension of 2,5-bis 4-carboxyphenyl furan diacid chloride (0.69g, 0.002mol) in 75 ml dry CH2CI2 a substituted diamine (0.002 mol) was added, the mixture was stirred at room temperature for 6 h.

The solvent was removed by distillation, the residue was treated with ice- water, the pH of the mixture was adjusted to 10 with 2M NaOH and the separated solid was filtered, washed with cold water and crystallized from ether: CHCI3 or ether : methanol to yield pale yellow solids in yields of 75-85%.

The free base was converted to its HCI salt by treating with saturated ethanolic-HCI in yields of 75-90%.

Example 21 2,5-Bis- [4- (3- (N-morpholinopropyl) carbamoyl) phenyl] furan dihydrochloride (Compound 33) An 83% yield of yellow crystalline solid mp 140-142°C dec was obtained using a procedure described above. The following data was obtained:'H NMR (DMSO-d6/D2O) 7.93 (d, 4H, J = 8.4), 7.86 (d, 4H, J = 8.4), 7.15 (s, 2H), 3.86 (br m, 8H), 3.38 (br m, 12H), 3.16 (t, 4H, J = 7.6), 2.0 (quintet, 4H, J = 7.6).'3C NMR (DMSO-d6/D2O) 166.5,152.7,133.1,132.4, 128.0,123.4,110.0,63.3,54.3,51.3,36.6,23.4. MS m/e 560 (M+). Anal. calcd. for C32H40N4Os ! 2HCI C, 60.65; H, 6.68; N, 8.84. Found: C, 60.59; H, 6.77; N, 8.87.

Example 22 2,5-Bis [4- (2-N, N-dimethylaminoethylcarbamoyl) phenyl] furan dihydrochloride (Compound 34) The procedure used for Example 21 was followed and an 80% yield of pale yellow crystalline solid mp 189-191 °C dec was obtained. The following

data was obtained:'H NMR (DMSO-d6/D2O) 7.94 (d, 4H, J = 8.4), 7.84 (d, 4H, J = 8.4), 7.12 (s, 2H), 3.66 (t, 4H, J = 6.0), 3.30 (t, 4H, J = 6.0), 2.84 (s, 12H).'3C NMR (DMSO-d6/D2O) 167.4,152.9,132.9,132.7,128.4,123.7, 110.4,56.6,43.1,34.9. MS m/e 448 (M+). Anal. calcd. for C26H32N403! 2HCI C, 59.88; H, 6.57; N, 10.74,. Found: C, 59.78; H, 6.66; N, 10.64.

Example 23 2,5-Bis [4- (3-N, N-dimethylaminopropylcarbamoyl) phenyl] furan dihydrochloride (Compound 35) The procedure used in Example 21 was followed and a 75% yield of yellow hygroscopic solid mp 205-208°C dec was obtained. The following data were also obtained:'H NMR (DMSO-d6) 10. 91 (br, 2H), 8.80 (b s 2H), 8.03 (d, 4H, J = 8.4), 7.92 (d, 4H, J = 8.4), 7.23 (s, 2H), 3.40 (q, 4H, J = 6), 3.15 (quintet, 4H, J = 5.2), 2.76 (s, 6H), 2.75 (s, 6H), 2.02 (quintet, 4H, J = 6.8).

'3C NMR (DMSO-d6/D2O) 165.6,152.4,132.8,131.9,127.7,122.9,109.6, 54.3,41.7,36.2,23.8. MS m/e 476 (M+). Anal. calcd. for C28H36N403! 2HCI! 0.5 H20 C, 60.21; H, 7.03; N, 10.03. Found: C, 60.51; H, 7.13; N, 9.95.

Example 24 2,5-Bis [4- (3-N-methyl-3-N-phenylaminopropylcarbamoyl) phenyl] furan dihydrochloride (Compound 36) The procedure used for Example 21 was employed and a 78% yield of yellow solid, 85-88°C dec was obtained. The following data was also obtained:'H NMR (DMSO-d6/D2O) 7.93 (d, 4H, J = 8.4), 7.89 (d, 4H, J = 8.4), 7.58 (d, 2H, J = 8.8), 7.55-7.48 (m, 6H), 7.37 (S, 2H), 7.18 (s, 2H), 3.59 (m, 4H), 3.35 (t, 4H, J = 7.2), 3.16 (s, 6H), 1.83 (quintet, 4H, J = 7.2).'3C NMR (DMSO-d6/D2O) 166.4,152.7,133.1,132.4,130.1,130. 0,128.0,123. 4, 119.7,109.9,55.3,43.6,36.5,25.3. MS m/e. Anal. calcd for: C38H4oN403! 2HCI ! 0. 75H2O C; 66.37; H, 6.34; N, 8.15. Found: C, 66.43; H, 6.34; N, 8.21.

Example 25 2,5-Bisl4-(3-N, N8, N"-trimethylaminopropylcarbamoyl) phenyl] furan dihydrochloride (Compound 37) The procedure used in Example 21 was employed and an 85% yield of yellow solid mp245-247°C dec was obtained. The following data were also obtained:'H NMR (DMSO-d6/D2O) 7.82 (d, 4H, J = 8), 7.56 (d, 4H, J = 8), 7.07 (s, 2H), 3.5-3.48 (m, 4H), 3.03 (brm, 4H), 2.94 (s, 6H), 2.76 (s, 12H), 1.98 (quintet, 4H, J = 7.6).'3C NMR (DMSO-d6/D2O) 171.2,152.8,135. 4, 131.2,127.9,123.8,109.7,54.9,42. 7,38.7,22. 4. MS m/e 504 (M+). Anal.

Calcd. For: C30H40N403 ! 2HCI ! 0. 5H2O. C, 61.42; H, 7.38; N, 9.45. Found: C, 61.11; H, 7.27; N, 9.61.

Example 26 2,5-Bis 3-amidinophenyl furan dihydrochloride (Compound 38) A suspension of the imidate ester dihydrochloride (0.87 g, 0.002 mol), prepared from 2,5-bis 3-cyanophenyl furan in 30 ml absolute ethanol was saturated with dry ammonia at 0-5°C and the mixture was stirred at room temperature for 2 h. The solvent was removed and the solid treated with ice-water, filtered, basified with cold aqueous 2 M NaOH and the off-white precipitate which formed was filtered. The solid washed with water and dried to yield 0.49 g (80.6%), mp 198-200 C. The free base (0.3 g, 0.001 mol) was converted into the HCI salt by treating with ethanolic HCI to yield 0.35 g (90%) mp 221-224°C dec. the following data was obtained:'H NMR (DMSO-d6/D2O) 8.18 (br s, 2H), 8.10 (d, 2H, J = 7.6), 7.68 (t, 2H, J = 7.6), 7.64 (d, 2H, J = 7.6), 7.14 (s, 2H).'3C NMR (DMSO-d6) 166.1,152.5,131.3, 130.6,129.3,129.0,127.4,123.3,110.5. MS (FAB) m/e 305 (M++1). Anal.

Calcd. For: C18H,16N4Ol2HCl!0.25H2O#C, ; H, 4.88; N, 14.67. Found: C, 56.75; H, 4.84; N, 14.26.

Example 27 2,5-Bis- [3- (N-isopropylamidino) amidinophenyl] furan dihydrochloride (Compound 40) The imidate ester hydrochloride (0.435 g, 0.001 mol), prepared from 2,5-bis 3-cyanophenyl furan and isopropyl amine (0.124 g, 0.0022 mol) in 10 ml ethanol were stirred for 12 h and yielded, after standard work-up, 0.13 g (80%) of beige free base having a mp 180-181 C (crystallized from hexane: ether 3: 1). The free base on treatment with saturated ethanolic HCI yielded 0.29 g (75%) crystalline solid, mp 225-227 C dec. The following addition data were also obtained:'H NMR (DMSO-d6) 8.18-8.12 (m, 4H), 7.71-7.62 (m, 4H), 7.27 (s, 2H), 4.09 (quintet, 2H, J = 6.4), 1.30 (d, 12H, J = 6.4).'3C NMR (DMSO-d6) 161.6,152.1,130.4,129.9,129.7,127.9,127.3, 123.3,110.1,45.2,21.2. MS (FAB) m/e 339 (M'+ 1). Anal. calcd. for: C24H28N40! 2HCI! 0.25 H20 (465.92) C, 61.86; H, 6.59; N, 12.02. Found: C, 61.82; H, 6.27; N, 11.76.

Example 28 2,5-Bis [3 (N-(2-dimethylaminoethyl) amidino phenylfuran dihydrochloride (Compound 41) A mixture of imidate ester hydrochloride (0.435 g, 0.001 mol), prepared from 2,5-bis 3-cyanophenyl furan and 2-dimethylaminoethylamine (0.185g, 0.0021 mol) in 10 ml ethanol was stirred at room temperature for 12 h.

Subsequent to standard work up, 0.33g (74%) crystalline solid mp 75-77°C was obtained. The free base (0.30 g, 0.00072 mol) on treatment with saturated ethanolic HCI yielded 0.35 g (82%) of hydrochloride salt (very hygroscopic) which was dried at 75°C for 24 h; mp 260-263°C dec. The following additional data were also obtained:'H NMR (DMSO-d6) 8.28 (brs, 2H), 8.12 (d, 2H, J = 8), 7.72 (d, 2H, J = 8), 7.65 (t, 2H, J = 8), 7.21 (s, 2H), 3.9 (t, 4H, J = 4.2), 3.50 (t, 3H, J = 4.2), 2.89 (s, 12H)."C NMR (DMSO-d6) 164.1,152.4,130.9,130.3,129.6,128.8,127.6,123.7,110.5, 54.5,43.2,38.4. MS (FAB) m/e 447 (M+ +1). Anal. calcd. for: C26H34N60 ! 4HCI (592.44) C, 52.70; H, 6.46; N, 14.19. Found: C, 52.43; H, 6.42; N, 13.99.

Examples 1-20 Antifungal Test Results Antifungal susceptibility testing for compounds set forth in Examples 1- 20 is discussed hereinbelow. The fungi that were employed included two reference strains, C. neoformans var. neoformans H99 and C. albicans A39 and the following clinical isolates: (1) two strains of fluconazole-resistant C. neoformans var. neoformans (135. 95 and 114.96); (2) two strains of C. neoformans var. gattii (119.95 and 114.95); (3) two strains of fluconazole- resistant C. albicans (102.96 and 103.96); and (4) one strain each of Torulopsis glabrata (142.91), Candida parapsilosis (111.96), Candida krusei (132.91), C. tropicalis (110.96), Candida lusitaniae (111.92), Fusarium solani (152.89), Aspergillus fumigatus (168.95), and Aspergillus flavus (112.96).

Antifungal susceptibility testing was performed using an RPMI-1640 medium (Sigma Chemical Co., St. Louis, MO) with glutamine, without sodium bicarbonate, and buffered at pH 7.0 with 0.165 M morpholine-propanesulfonic acid (MOPS).

In vitro susceptibility testing in the form of Minimum Inhibitory Concentration (MIC) experiments were performed using the broth macrodilution method according to the recommendations of the National Committee for Clinical Laboratory Standards (see 1995 manual). The only difference compared to the standardized procedure was the choice of drug dilutions ranging from 100 to 0.09 pg/ml. Briefly, this procedure specifies an inoculum grown at 35°C and adjusted to a concentration of 0.5-2.5 x 103 CFU/ml with an incubation of the test performed at 35°C and reading at 48 hours for all yeasts except for C. neoformans which is interpreted at 72 hr.

The MIC was defined as the lowest drug concentration which showed a visual turbidity less than or equal to an 80 percent inhibition compared to that produced by the growth control tube.

Minimum Fungicidal Concentration (MFC) experiments were adapted from a method by McGinnis (McGinnis, M. R., (1980)"Susceptibility testing and bioassay procedure", p. 431, Academic Press, Inc., New York). Briefly, 10, ul aliquots from tubes with growth inhibition were plated onto Sabouraud agar plates. The lowest drug concentration that yielded three or fewer yeasts colonies was recorded as the MFC.

Molds were tested by the National Committee for Clinical Laboratory Standards method cited above using the below-referenced modifications.

Isolates were grown on Sabouraud dextrose agar at 30°C and subcultured twice to insure viability. After adequate sporulation occurred (4-12 days), conidia were harvested by flooding colonies with a sterile solution of 0.85 percent NaCI and 0.05 percent Tween 80 in sterile distilled water. Inocula were prepared using a hemocytometer for counting, then diluted with RPMI 1640 medium to obtain a final inoculum size of approximately 0.5-2.5 x 103 CFU/ml.

The inoculum size was verified by plating an aliquot of the inoculum. Tests were incubated at 30°C for 48-72 h or until growth in the control tube was visible. In each experiment, the quality control included the testing of C. albicans A 39 and C. neoformans H99 against fluconazole and amphotericin B.

Examples 21-28 Antifungal Test Results Antifungal susceptibility testing for compounds set forth in Examples 21-28 is discussed hereinbelow. The fungi that were employed included two quality control reference strains, C. neoformans var. neoformans H99 and C. albicans A39 and the following clinical isolates: (1) four strains of C. neoformans var. neoformans (167.95; 135.95; 114.96; and 133.95) of which three were fluconazole-resistant >64, ug/ml (135.95; 114.96; and 133.95); (2) two strains of C. neoformans var. gattii (119.95 and 114.95); (3) two strains of fluconazole-resistant >64, ug/ml C. albicans (102.96 and 103.96); and (4) one strain each of C. glabrata (142.91), Candida parapsilosis (111.96), Candida krusei (132.91), C. tropicalis (110.96), Candida lusitaniae (111.92),

Fusarium solani (152.89), Aspergillus fumigatus (168.95), Rhizopus arrhizus (117.89), Paecilomyces lilacinus (137.90), and Aspergillus flavus (112.96).

Antifungal susceptibility testing was performed using an RPMI-1640 medium (Sigma Chemical Co., St. Louis, MO) with glutamine, without sodium bicarbonate, and buffered at pH 7.0 with 0.165 M morpholinepropanesulfonic acid (MOPS).

In vitro susceptibility testing in the form of Minimum Inhibitory Concentration (MIC) experiments were performed using the broth macrodilution method according to the recommendations of the National Committee for Clinical Laboratory Standards (see 1995 manual). The only difference compared to the standardized procedure was the choice of drug dilutions ranging from 100 to 0.09, ug/ml. Briefly, this procedure specifies an inoculum grown at 35°C and adjusted to a concentration of 0.5-2.5 x 103 CFU/ml with an incubation of the test performed at 35°C and reading at 48 hours for all yeasts except for C. neoformans which is interpreted at 72 hr.

The MIC was defined as the lowest drug concentration which showed a visual turbidity less than or equal to an 80 percent inhibition compared to that produced by the growth control tube.

Minimum Fungicidal Concentration (MFC) experiments were adapted from a method by McGinnis (McGinnis, M. R., (1980)"Susceptibility testing and bioassay procedure", p. 431, Academic Press, Inc., New York). Briefly, 10 pl aliquots from tubes with growth inhibition were plated onto Sabouraud agar plates. The lowest drug concentration that yielded 3 or fewer yeasts colonies was recorded as the MFC. Several drugs were also rescreened with a subculture of 100 ul aliquots from tubes with no growth and there was no change in MFC.

Molds were tested by the National Committee for Clinical Laboratory Standards method cited above using the below-referenced modifications.

Isolates were grown on Sabouraud dextrose agar at 30°C and subcultured twice to insure viability. After adequate sporulation occurred (4-12 days),

conidia were harvested by flooding colonies with a sterile solution of 0.85 percent NaCI and 0.05 percent Tween 80 in sterile distilled water. Inoculum suspensions were prepared using a hemocytometer for counting, then diluted with RPMI 1640 medium to obtain a final inoculum size of approximately 0.5- 2.5 x 103 CFU/ml. The inoculum size was verified by plating an aliquot of the final concentration. Tests were incubated at 30°C for 48-72 h or until growth in the control tube was visible. The reproducibility of the method was quality controlled by testing fluconazole and amphotericin B against C. albicans A39 and C. neoformans H99 in each experiment. MlCs for fluconazole against C. albicans A39 and C. neoformans H99 were 0.25 ug/ml and 2 ug/ml respectively. Miss for amphotericin B were 1 ug/ml against both isolates.

Tables 1-9 illustrate the antifungal activity according to the methods of the invention. As shown therein, the compounds used in the methods of the invention are effective in combating fungal infections, particularly in comparison to amphotericin, fluconazole, and pentamidine.

In the specification, and examples there have been disclosed typical preferred embodiments of the invention and, although specific terms are employed, they are used in a generic and descriptive sense only and not for the purposes of limitation, the scope of the invention being set forth in the following claims: