WO2001029010A1

WO2001029010A1 - Gram-positive selective antibacterial compounds, compositions containing such compounds and methods of treatment

Info

Publication number: WO2001029010A1
Application number: PCT/US2000/028809
Authority: WO
Inventors: Amjad Ali; Gayle E. Taylor; Donald W. Graham
Original assignee: Merck & Co., Inc.
Priority date: 1999-10-21
Filing date: 2000-10-18
Publication date: 2001-04-26
Also published as: AU2247701A

Abstract

The compounds of formula (I) including pharmaceutically acceptable salts, stereoisomers or esters thereof are disclosed.

Description

TITLE OF THE INVENTION

GRAM-POSITIVE SELECTIVE ANTIBACTERIAL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT

BACKGROUND OF THE INVENTION

DNA polymerase m (DNA pol HI) enzyme has been shown to be crucial in the replicative DNA synthesis of Gram-positive bacteria. Since DNA pol HI shows little homology to mammalian or gram-negative bacterial DNA polymerases it represents an attractive target for inhibition in the discovery of new Gram-positive selective antibacterial agents.

G.E. Wright et al., J. Med. Chem 1974, 12, 1277-1282; 1977, 20, 1181- 1185; 1980, 23, 34-38;and 1984, 27, 181-185; Pharmac Ther. 1990, 47, 447-497; and Nucleic acids research 1990, 24, 7381 have reported on a series of guanine and uracil based DNA pol HI inhibitors. See also WO 96/06614. Inhibitory action of these compounds is reversed by specific purine deoxyribonucleoside 5'-triphosphates, dGTP in the case of uracil derivatives and dATP in the case of isocytosines. Enzyme inhibition results directly from the immobilization of pol HI in a ternary complex composed of the DNA template, the inhibitor and the enzyme (see, e.g., G. Wright, et al, J. Med. Chem 1974, 12, 1277-1282). However, these compounds are insoluble and contain unsuitable functionalities and therefore unattractive.

The present invention relates to DNA polymerase HI inhibitors which are useful against gram positive microorganisms, especially methicillin resistant Staphylococcus aureus (MRSA), methicillin resistant Staphylococcus epidermidis (MRSE), B. subtilis, Enterococcus fecalis/fecium, Streptococus pneumoniae and methicillin resistant coagulase negative Staphylococci (MRCNS). The compounds represent a novel class of DNA pol HI inhibitors which have advantages with respect to efficacy, toxicity and/or metabolism. The antibacterial compounds of the present invention thus comprise an important contribution to therapy for treating infections caused by these difficult to control pathogens. There is an increasing need for agents effective against such pathogens (MRSA/MRCNS) which are at the same time relatively free from undesirable side effects. SUMMARY OF THE INVENTION

The compounds of the invention are represented by formula I:

I including pharmaceutically acceptable salts, stereoisomers or esters thereof, wherein:

R¹ represents H, Ci-10 alkyl, C2-10 alkenyl, C2-10 alkynyl, (CH2)nC3-10 alicyclic, (CH2)_nC3-10 heterocyclic, (CH2)_nC5-10 aryl, (CH2)_nC5-lθheteroaryl, (CH₂)_ndiaryl, (CH₂)_nOR², (CH₂)mCO₂R², (CH₂)_nN(R2)₂, (CH₂)_nCON(R2)₂,

said alkyl, alkenyl, alkynyl, aryl, heteroaryl, optionally substituted with 1 to 3 groups of R^a; and providing that when R¹ is H, CH3, CH2CH3, CH2CH=CH2 or (CH2)2-5CH3, R3 cannot be 3,4-trimethyleneanilino or when R! is H, CH3, CH2CH3, CH2CH-CH2 or (CH2)2-5CH3, R3 cannot be 3-ethyl-4-methylanilino;

m is 0 to 5; n is 0 to 5; p is 0 to 2;

R2 represents H, Ci-10 alkyl;

3 R is C3-ioalicyclic, C3-ioheterocyclic, (CH2)nC5-10aryl,

(CH2)_nC5-10 heteroaryl, NH(CH2)_nC5-10^aryl, or NH(CH2)_nC5-lθheteroaryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R;

R is H, C 1 -6 alkyl, C 1 -6 alkyl-OH, halo, C 1 -6 alkylhalo, OR², CN,

CF3, N(R²)2, CO2R², NO2, NHCOR², SO2R² or SR²; R^a represents Ci-io alkyl, C3-8 cycloalkyl, halo, C1 -6 alkyl-OH, OH, C1-6 alkylhalo, CF3, NH2, C1 -6 alkylNH₂, -SH, -SC_]-4alkyl, -CN, -COC,_-8alkyl, -C_5-ιo aryl, -COC -ι₀ aryl, -Cs-io heteroaryl, -COC₅.10 heteroaryl,

CONR⁶R⁷, NHCOR², OCOR⁶, -NR⁶(CO)R⁷, NR⁶(CO)NHR⁷, NHSO₂R⁶, OR⁶, CO₂R⁶, or NR⁶R^{7 and}

R⁶ & R⁷ independently represent H, Cι _8 alkyl, C3-8 cycloalkyl, or - C5-10 aryl.

DETAILED DESCRIPTION OF THE INVENTION

The invention is described herein in detail using the terms defined below unless otherwise specified. The term "alkyl" refers to a monovalent alkane (hydrocarbon) derived radical containing from 1 to 15 carbon atoms unless otherwise defined. It may be straight or branched, saturated or unsaturated. Preferred alkyl groups include methyl, ethyl, propyl, hexyl, isopropyl, butyl and t-butyl. When substituted, alkyl groups may be substituted with up to 3 substituent groups, selected from R^a as defined, at any available point of attachment. When the alkyl group is said to be substituted with an alkyl group, this is used interchangeably with "branched alkyl group".

Cycloalkyl is a specie of alkyl containing from 3 to 15 carbon atoms, without alternating or resonating double bonds between carbon atoms. It may contain from 1 to 4 rings which are fused. Preferred cycloalkyl groups are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. When substituted, cycloalkyl groups may be substituted with up to 3 substituents selected from R^a as defined.

The term unsaturated alkyl refers to "alkenyl" or "alkynyl". The term "alkenyl" refers to an unsaturated alkyl such as a hydrocarbon radical, straight or branched containing from 2 to 6 carbon atoms and at least one carbon to carbon double bond. Preferred alkenyl groups include propenyl, hexenyl and butenyl. The term "alkynyl" refers to an unsaturated alkyl such as a hydrocarbon radical straight or branched, containing from 2 to 16 carbon atoms and at least one carbon to carbon triple bond. Preferred alkynyl groups include propynyl, hexenyl and butynyl. The term "alicyclic" refers to non-aromatic monocyclic or bicyclic C3- C10 hydrocarbons, including unsaturated, which can be substituted with 0-3 groups of R. Examples of said groups include cycloalkyls such as cyclohexyl, cyclopentyl, bicyclo[2.2.1]heρtyl, bicyclo[2.2.1]hepta-2,5-dienyl, bicyclo[2.2.2]octyl, bicyclo[2.2.2]octa-2,5-dienyl.

The term "heterocyclic" refers to a monocyclic non-aromatic moiety containing 3-8 ring atoms or a bicyclic non-aromatic moiety containing 6-10 ring atoms, at least one of which ring atoms is a heteroatom selected from nitrogen, oxygen and sulfur and where one additional ring atom may be oxygen or sulfur. Examples of heterocyclic groups are furanyl, pyranyl, morpholinyl, dioxanyl and quinuclidinyl.

Aryl refers to aromatic rings e.g., phenyl, substituted phenyl and the like, as well as rings which are fused, e.g., naphthyl, phenanthrenyl and the like. An aryl group thus contains at least one ring having at least 6 atoms, with up to five such rings being present, containing up to 22 atoms therein, with alternating (resonating) double bonds between adjacent carbon atoms. The preferred aryl groups are phenyl, naphthyl and phenanthrenyl. Aryl groups may likewise be substituted as defined. Preferred substituted aryls include phenyl and naphthyl.

The term "heteroaryl" (Het) refers to a monocyclic aromatic hydrocarbon group having 5 or 6 ring atoms, or a bicyclic aromatic group having 8 to 10 atoms, containing at least one heteroatom, O, S or N, in which a carbon or nitrogen atom is the point of attachment, and in which one or two additional carbon atoms is optionally replaced by a heteroatom selected from O or S, and in which from 1 to 3 additional carbon atoms are optionally replaced by nitrogen heteroatoms, said heteroaryl group being optionally substituted as described herein. Examples of this type are pyrrole, pyridine, oxazole, thiazole benzimidazolyl, and oxazine. Additional nitrogen atoms may be present together with the first nitrogen and oxygen or sulfur, giving, e.g., thiadiazole. Heteroaryl groups may likewise be substituted with 1 to 3 groups of R^a as defined. Examples include the following: N r^;^ N, H N r- % pyrrole (pyrrolyl) pmidazole (imidazolyl) thiazole (thiazolyl)

oxazole (oxazolyl) furan (furyl) thio ophene (thienyl)

X NH tπazole (tπazolyl) pyrazole (pyrazolyl) isoxazole (tsoxazolyl)

isothiazole (isothiazolyl) pyπdine (pyπdinyl) pyrazme (pyrazinyl)

N pyπmidine pyπdazine (pyπdazinyl) (pyπmidinyl) triazme (tπazinyl)

The term "heteroatom" means O, S or N, selected on an independent basis. Halogen and "halo" refer to bromine, chlorine, fluorine and iodine.

When a group is termed "substituted", unless otherwise indicated, this means that the group contains from 1 to 3 substituents thereon.

When a functional group is termed "protected", this means that the group is in modified form to preclude undesired side reactions at the protected site. Suitable protecting groups for the compounds of the present invention will be recognized from the present application taking into account the level of skill in the art, and with reference to standard textbooks, such as Greene, T. W. et al. Protective Groups in Organic Synthesis Wiley, New York (1991). Examples of suitable protecting groups are contained throughout the specification. Some of the compounds of the present invention may be protected by protecting groups. Conventional protecting groups consist of groups which are used to protectively block the hydroxyl or carboxyl group during the synthesis procedures described herein. These conventional blocking groups are readily removable, i.e., they can be removed, if desired, by procedures which will not cause cleavage or other disruption of the remaining portions of the molecule. Such procedures include chemical and enzymatic hydrolysis, treatment with chemical reducing or oxidizing agents under mild conditions, treatment with a transition metal catalyst and a nucleophile and catalytic hydrogenation. Examples of carboxyl protecting groups include allyl, benzhydryl, 2-naphthylmethyl, benzyl, silyl such as t-butyldimethylsilyl (TBDMS), phenacyl, p-methoxybenzyl, o-nitrobenzyl, p-methoxyphenyl, p-nitrobenzyl, 4-pyridylmethyl and t-butyl.

Examples of suitable hydroxy protecting groups include triethylsilyl, t- butyldimethylsilyl, o-nitrobenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, benzyloxycarbonyl, allyloxycarbonyl, t-butyloxycarbonyl, 2,2,2- trichloroethyloxycarbonyl and the like. The compounds of the present invention are useful per se and in their pharmaceutically acceptable salt and ester forms for the treatment of bacterial infections in animal and human subjects. The term "pharmaceutically acceptable ester, salt or hydrate," refers to those salts, esters and hydrated forms of the compounds of the present invention which would be apparent to the pharmaceutical chemist, i.e., those which are substantially non-toxic and which may favorably affect the pharmacokinetic properties of said compounds, such as palatability, absorption, distribution, metabolism and excretion. Other factors, more practical in nature, which are also important in the selection, are cost of the raw materials, ease of crystallization, yield, stability, solubility, hygroscopicity and flowability of the resulting bulk drug. Conveniently, pharmaceutical compositions may be prepared from the active ingredients in combination with pharmaceutically acceptable carriers. Thus, the present invention is also concerned with pharmaceutical compositions and methods of treating bacterial infections utilizing as an active ingredient the novel carbapenem compounds. The pharmaceutically acceptable salts referred to above may take the form of a negative charge, which is balanced by a counterion, e.g., an alkali metal cation such as sodium or potassium. Other pharmaceutically acceptable counterions may be calcium, magnesium, zinc, ammonium, or alkylammonium cations such as tetramethylammonium, tetrabutylammonium, choline, triethylhydroammonium, meglumine, triethanolhydroammonium, etc.

The pharmaceutically acceptable salts referred to above also include acid addition salts. Thus, the Formula I compounds can be used in the form of salts derived from inorganic or organic acids. Included among such salts are the following: acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2- hydroxyethanesulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, pamoate, pectinate, persulfate, 3-phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, thiocyanate, tosylate and undecanoate.

Acid addition salts of the compounds of formula I include compounds that contain a protonated, basic moiety. Compounds containing a basic moiety are capable of protonation in aqueous media near pH 7, so that the basic moiety can exist as an equilibrium mixture of its neutral form and acid addition (protonated) form. The more basic the group, the greater the degree of protonation near pH 7. All such compounds are included in the present invention.

The pharmaceutically acceptable esters are such as would be readily apparent to a medicinal chemist, and include, for example, those described in detail in U.S. Pat. No. 4,309,438. Included within such pharmaceutically acceptable esters are those which are hydrolyzed under physiological conditions, such as pivaloyloxymethyl, acetoxymethyl, phthalidyl, indanyl and methoxymethyl, and others described in detail in U.S. Pat. No. 4,479,947. These are also referred to as "biolabile esters".

Biolabile esters are biologically hydrolizable, and may be suitable for oral administration, due to good absorption through the stomach or intenstinal mucosa, resistance to gastric acid degradation and other factors. Examples of biolabile esters include compounds in which M represents an alkoxyalkyl, alkylcarbonyloxyalkyl, alkoxycarbonyloxyalkyl, cycloalkoxyalkyl, alkenyloxyalkyl, aryloxyalkyl, alkoxyaryl, alkylthioalkyl, cycloalkylthioalkyl, alkenylthioalkyl, arylthioalkyl or alkylthioaryl group. These groups can be substituted in the alkyl or aryl portions thereof with acyl or halo groups. The following M species are examples of biolabile ester forming moieties.: acetoxymethyl, 1-acetoxyethyl, 1-acetoxypropyl, pivaloyloxymethyl, 1 -isopropyloxycarbonyloxyethyl, 1 -cyclohexyloxycarbonyl- oxyethyl, phthalidyl and (2-oxo-5-methyl-l,3-dioxolen-4-yl)methyl. A subset of compounds of formula I which is of interest relates to those compounds where R represents Cj_-8 alkyl, C _-8 alkenyl, (CH2)nC5-10 aryl, or (CH2)nC5-lO alicyclic, said alkyl, alkenyl, aryl or alicyclic optionally substituted with 1-3 groups of R^a. Within this subset, all other variables are as originally defined. Another subset of compounds of formula I which is of interest relates 3 to those compounds where R is C3-I oalicyclic, (CH2)nC5-ioaryl_;

(CH2)nC5-lθh.eteroaryl, or NH(CH2)nC5-lθaryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R. Within this subset, all other variables are as originally defined.

A preferred subset of compounds of formula I that is of interest relates to compounds where R represents Cι_-8 alkyl, C _-8 alkenyl, (CH2)nC5-lθ aryl, or

(CH2)nC5-10 alicyclic, said alkyl, alkenyl, aryl or alicyclic optionally substituted with

3 1-3 groups of R^a; and R represents C3-I oalicyclic, (CH2)nC5-l()aryl₅ (CH2)nC5-lθheteroaryl, or NH(CH2)nC5-10aryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R, optionally substituted with 1 to 3 groups of R. Within this subset, all other variables are as originally defined.

Also included in this invention is a pharmaceutical composition comprised of a compound in accordance with formula I in combination with a pharmaceutically acceptable carrier.

Also included in this invention is a method of treating a bacterial infection comprising administering to a mammalian patient in need of such treatment a compound as defined in claim 1 in an amount which is effective for treating a bacterial infection. Still included within the scope of this invention is a method of treating a bacterial infection involving methicillin resistant Staphylococcus aureus, methicillin resistant Staphylococcus epidermidis, B. subtilis, Enterococcus facalis/fecium, Streptococcus pneumoniae, methicillin resistant coagulase negative Staphylococci microoganisms or any combination thereof comprising administering to a mammalian patient in need of such treatment a compound of formula I in an amount which is effective for treating a bacterial infection.

Representative examples of compounds of the invention are found in Table I. TABLE 1

Table 1 Cont'd

The process is illustrated using the general conditions shown in the accompanying flow chart.

Flow Chart A:

1

POCI₃

Δ H₂O

With reference to Flow Chart A above Ri and R₂ are defined with respect to the compounds of Formula I. The compounds of the present invention wherein Ri is ethyl and R₃ is 3-iodo-4-methyl phenyl, can be prepared by reacting ethylurea with malonic acid in the presence of acetic anhydride and acetic acid to give N-ethyl barbituric acid 1. Further reaction with phosphorus oxychloride and water affords chloride 2 which is treated with the appropriately substituted amine using 2- methoxyethanol and water as the co-solvent to yield the desired compounds of Formula I.

The synthesis of the target compound is completed by removing any protecting groups which are present in the penultimate intermediate using standard techniques which are well known to those skilled in the art. The deprotected final product is then purified, as necessary, using standard techniques such as ion exchange chroma-tography, HPLC on reverse phase silica gel, MPLC on reverse phase polystyrene gel, and the like or by recrystallization.

The final product may be characterized structurally by standard techniques such as ΝMR, IR, MS, and UV. For ease of handling, the final product, if not crystalline, may be lyophilized from water to afford an amorphous, easily handled solid. The compounds of the present invention are valuable antibacterial agents active against various Gram-positive and to a lesser extent Gram-negative bacteria, and accordingly find utility in human and veterinary medicine.

Many of compounds of the present invention are biologically active against MRSA/MRCNS. In vitro antibacterial activity is predictive of in vivo activity when the compounds are administered to a mammal infected with a susceptible bacterial organism.

Using standard susceptibility tests, the compounds of the invention are determined to be active against MRSA. The compounds of the invention can be formulated in pharmaceutical compositions by combining the compound with a pharmaceutically acceptable carrier. Examples of such carriers are set forth below.

The compounds may be employed in powder or crystalline form, in liquid solution, or in suspension. They may be administered by a variety of means; those of principal interest include: topically, orally and parenterally by injection (intravenously or intramuscularly).

Compositions for injection, a preferred route of delivery, may be prepared in unit dosage form in ampules, or in multidose containers. The injectable compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain various formulating agents. Alternatively, the active ingredient may be in powder (lyophillized or non- lyophillized) form for reconstitution at the time of delivery with a suitable vehicle, such as sterile water. In injectable compositions, the carrier is typically comprised of sterile water, saline or another injectable liquid, e.g., peanut oil for intramuscular injections. Also, various buffering agents, preservatives and the like can be included.

Topical applications may be formulated in carriers such as hydrophobic or hydrophilic bases to form ointments, creams, lotions, in aqueous, oleaginous or alcoholic liquids to form paints or in dry diluents to form powders. Oral compositions may take such forms as tablets, capsules, oral suspensions and oral solutions. The oral composions may utilize carriers such as conventional formulating agents, and may include sustained release properties as well as rapid delivery forms. The dosage to be administered depends to a large extent upon the condition and size of the subject being treated, the route and frequency of administration, the sensitivity of the pathogen to the particular compound selected, the virulence of the infection and other factors. Such matters, however, are left to the routine discretion of the physician according to principles of treatment well known in the antibacterial arts. Another factor influencing the precise dosage regimen, apart from the nature of the infection and peculiar identity of the individual being treated, is the molecular weight of the compound.

The compositions for human delivery per unit dosage, whether liquid or solid, may contain from about 0.01% to as high as about 99% of active material, the preferred range being from about 10-60%. The composition will generally contain from about 15 mg to about 2.5 g of the active ingredient; however, in general, it is preferable to employ dosage amounts in the range of from about 250 mg to 1000 mg. In parenteral administration, the unit dosage will typically include the pure compound in sterile water solution or in the form of a soluble powder intended for solution, which can be adjusted to neutral pH and isotonic.

The invention described herein also includes a method of treating a bacterial infection in a mammal in need of such treatment comprising administering to said mammal a compound of formula I in an amount effective to treat said infection.

The preferred methods of administration of the Formula I antibacterial compounds include oral and parenteral, e.g., i.v. infusion, i.v. bolus and i.m. injection. For adults, about 5-50 mg of Formula I antibacterial compound per kg of body weight given one to four times daily is preferred. The preferred dosage is 250 mg to 1000 mg of the antibacterial given one to four times per day. More specifically, for mild infections a dose of about 250 mg two or three times daily is recommended. For moderate infections against highly susceptible gram positive organisms a dose of about 500 mg three or four times daily is recommended. For severe, life-threatening infections against organisms at the upper limits of sensitivity to the antibiotic, a dose of about 1000-2000 mg three to four times daily may be recommended.

For children, a dose of about 5-25 mg/kg of body weight given 2, 3, or 4 times per day is preferred; a dose of 10 mg/kg is typically recommended. The invention is further described in connection with the non-limiting examples below, wherein the concentration of solutions were carried out on a rotary evaporator under reduced pressure. Flash chromatography was carried out on silica gel (230-400 mesh). NMR spectra were obtained at ambient temperature in deuterated dimethyl sulfoxide unless otherwise indicated. Coupling constants (J) are in hertz (Hz). All temperatures given in the following examples are in degrees Celsius.

Abbreviations: diethyl ether (ether), room temperature (rt), hour(s) (h), minute(s) (min). "NMR," unless otherwise specified, refers to 1H nuclear magnetic resonance spectroscopy and "TLC" refers to thin-layer SiO₂ chromatography. "MS" refers to mass spectroscopy and "HPLC" refers to high-pressure liquid chromatography.

MS CONDITIONS

MS A. Samples were run on a Finnigan TSQ700 by Flow Injection Electrospray Ionization MS. Mobile phase: 82% AcN with 1.3M TFA-NH Formate.

MS B. Samples were run on a Finnigan SSQ710 by Flow Injection

Particle Beam Election Impact Ionization MS. Mobile phase: 80:20 MeOH:CH₂Cl .

HPLC CONDITIONS

HPLC A. Retention time using the following conditions: Column:

YMC ODS A, 5μ, 4.6 x 50 mm; Gradient Eluant: 10:90 to 90:10 v/v H₂O/CH₃CN + 0.5% TFA over 4.5 min, hold 30 sec; Detection: PDA, 210-400 nm; Flow Rate: 2.5 mL/min.

HPLC B. Retention time using the following conditions: Column:

YMC ODS A, 5μ, 4.6 x 33 mm C18; Gradient Eluant: 10:90 to 90:10 v/v H₂O/CH₃CN + 0.5%o TFA over 4.5 min, hold 30 sec; Detection: PDA, 210-400 nm; Flow Rate: 2.5 mL/min. EXAMPLE 1

Step A: Preparation of 1

1

A mixture of benzylurea (2 g, 13.32 mmol), malonic acid (1.61 g, 15.45 mmol) and glacial acetic acid (5 mL) was stirred at 70° for 1 h. Acetic anhydride (3 mL) was added dropwise over 10 min and the reaction stirred at 90° for a further 2 h. The reaction was concentrated in vacuo and the resultant residue triturated with EtOH (20 mL). The product was collected by filtration and the solid washed with EtOH (2 x 5 mL) and dried (vacuum oven, 60°) to afford 1 as a white powder. HPLC C: 1.92 min.

Step B: Preparation of 2

A mixture of N-benzylbarbituric acid 1 (1 g, 4.58 mmol) and phosphorus oxychloride (6 mL) was treated cautiously over 10 min with water (0.15 mL). The mixture was stirred at 135° for 1 h and the excess phosphorus oxychloride removed in vacuo. The remaining residue was poured into water (20 mL) and the crude product collected by filtration. Further purification by recrystallization from EtOH gave 2 as yellow powder. ΝMR: δ 5.08 (s, 2 H), 5.89 (s, 1 H), 7.28-7.47 (m, 5 H), 9.9 (bs, 1 H). HPLC C: 2.21 min. Step C: Preparation of 3

A mixture of 3-benzyl-6-chlorouracil 2 (50 mg, 0.21 mmol) and 3,4- dichlorobenzylamine (0.111 g, 0.63 mmol) in 2-methoxyethanol (3 mL) / H₂O (1 mL) was heated at reflux for 12 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with CHC1₃ (2 x 10 mL), dried (vacuum oven, 60°) and purified by chromatography on silica gel with EtOAC-hexane (1 :39) to afford 3 as a white powder. NMR: δ 4.30 (d, J 6.2 Hz, 2 H), 4.6 (bs, 1 H), 4.82 (bs, 2 H), 6.74 (s, 1 H), 7.19-7.34 (m, 6 H), 7.59-7.64 (m, 2 H), 10.6 (s, 1 H). HPLC C: 3.17 min.

EXAMPLE 2

Using the procedure in Example 1 , Step C 3-benzyl-6-chlorouracil 2 was reacted with 3-ethyl-4-methyl aniline [G. E. Wright et al, J. Med. Chem., 27, 181-185 (1984)] to afford 4 as light yellow powder. NMR: δ 1.12 (t, J7.6 Hz, 1 H), 2.22 (s, 3 H), 2.56 (q, J7.6 Hz, 2 H), 4.75 (s, 1 H), 4.87 (s, 2 H), 7.93-7.39 (m, 8 H), 8.21 (bs, 1 H), 10.48 (bs, 1 H). HPLC A: 3.28 min. EXAMPLE 3

Step A:

Using the procedure in Example 1 , Step A N-phenylurea was reacted with malonic acid to give N-phenylbarbituric acid 5. ΝMR: δ 3.71 (s, 2 H), 7.07-7.51 (m, 5 H), 11.5 (bs, 1 H). HPLC C: 3.09 min.

Step B:

Using the procedure in Example 1 , Step B N-phenylbarbituric acid 5 was reacted with phosphorus oxychloride to give 3-phenyl-6-chlorouracil 6. ΝMR: δ 5.99 (s, 1 H), 7.23-7.54 (m, 5 H), 8.46 (bs, 1 H). HPLC A: 1.89 min.

Step C:

Using the procedure in Example 1, Step C 3-phenyl-6-chlorouracil 6 was reacted with 3-ethyl-4-methyl aniline [G. E. Wright et al, J. Med. Chem., 27, 181-185 (1984)] to afford 7 as light yellow powder. NMR: δ 1.15 (t, J7.6 Hz, 1 H), 2.23 (s, 3 H), 2.58 (q, J7.6 Hz, 2 H), 4.77 (s, 1 H), 7.01-7.41 (m, 8 H), 8.12 (bs, 1 H), 10.56 (bs, 1 H). HPLC C: 2.75 min.

EXAMPLE 4

Using the procedure in Example 1, Step C 3-phenyl-6-chlorouracil 6 was reacted with 3,4-dichlorobenzylamine to afford 8 as a white powder. NMR: 4.32 (d, J6.2 Hz, 2 H), 4.61 (bs, 1 H), 6.84 (bs, 1 H), 7.11-7.38 (m, 2 H), 7.35-7.40 (m, 4 H), 7.62-7.69 (m, 2 H). HPLC C: 2.67 min.

EXAMPLE 5

Step A:

Using the procedure in Example 1 , Step A N-allylurea was reacted with malonic acid to give N-allylbarbituric acid 9. ΝMR: δ 4.25 (m, 4 H), 5.05 (dd, J 10.2 and 1.7 Hz, 1 H), 5.15 (dd, J 17.2 and 1.7 Hz, 1 H), 5.84 (ddt, J 17.2, 10.2 and 1.7 Hz, 1 H), 11.4 (bs, 1 H).

Step B:

10

Using the procedure in Example 1 , Step B N-allylbarbituric acid 9 was reacted with phosphorus oxychloride to give 3-allyl-6-chlorouracil 10. ΝMR: δ 4.25 (m, 2 H), 5.06 (m, 2 H), 5.85 (m, 1 H), 5.98 (s, 1 H), 12.38 (bs, 1 H). HPLC A: 1.17 min.

Step C:

11

Using the procedure in Example 1, Step C 3-allyl-6-chlorouracil 10 was reacted with 3-iodo-4-methyl aniline to afford 11 as a light yellow powder. NMR: δ 2.33 (s, 3 H), 4.27 (d, J5.2 Hz, 2 H), 4.74 (s, 1 H), 5.00-5.06 (m, 2 H), 5.74 (m, I H), 7.14 (dd, J8.2 and 2.1 Hz, I H), 7.31 (d, J 8.5 Hz, 1 H), 7.63 (d, J2.1 Hz, 1 H), 8.28 (bs, 1 H), 10.6 (bs, 1 H). HPLC C: 2.61 min.

EXAMPLE 6

12

A mixture of 3-ethyl-6-chlorouracil (100 mg, 0.57 mmol) [N. C. Brown et al, J. Med. Chem., 42, 2035-2040 (1999)] and 3-iodo-4-methylaniline (0.267 g, 1.80 mmol) in 2-methoxyethanol (6 mL) / H O (2 mL) was heated at reflux for 6 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1₃ (2 x 10 mL) and dried (vacuum oven, 60°) to afford 12 as a white powder. NMR: δ 1.04 (t, J6.9 Hz, 3 H), 2.32 (s, 3 H), 3.69 (q, J6.9 Hz, 2 H), 4.73 (s, 1 H), 7.16 (m, 1 H), 7.30 (d, J8.2 Hz, 1 H), 7.62 (bs, 1 H), 8.24 (bs, 1 H), 10.6 (bs, 1 H). HPLC A: 2.61 min. EXAMPLE 7

13

A mixture of 3-ethyl-6-chlorouracil (100 mg, 0.57 mmol) [N. C. Brown et al, J. Med. Chem., 42, 2035-2040 (1999)] and 3-bromo-4-methylaniline (0.267 g, 1.15 mmol) in 2-methoxyethanol (6 mL) / H O (2 mL) was heated at reflux for 6 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1₃ (2 x 10 mL) and dried (vacuum oven, 60°) to give 13 as a white powder. NMR: δ 1.03 (t, J6.9 Hz, 3 H), 2.31 (s, 3 H), 3.67 (q, J6.9 Hz, 2 H), 4.71 (s, 1 H), 7.14 (m, 1 H), 7.33 (d, J8.3 Hz, 1 H), 7.4 (bs, 1 H), 8.29 (bs, 1 H), 10.57 (bs, 1 H).

EXAMPLE 8

14

A mixture of 3-methyl-6-chlorouracil (40 mg, 0.25 mmole) [N. C. Brown et al, J. Med. Chem., 42, 2035-2040 (1999)] and 3-iodo-4-methylaniline (0.174 g, 0.75 mmol) in 2-methoxyethanol (3 mL) / H₂O (1 mL) was heated at reflux for 12 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1 (2 x 10 mL) and dried (vacuum oven, 60°) to give 14 as a white powder. NMR: δ 2.32 (s, 3 H), 3.05 (s, 3 H), 4.74 (s, 1 H), 7.15 (m, 1 H), 7.31 (d, J8.2 Hz, 1 H), 7.4 (s, 1 H), 8.26 (bs, 1 H), 10.61 (bs, 1 H). HPLC C: 2.37 min. EXAMPLE 9

15

A mixture of 3-propyl-6-chlorouracil (25 mg, 0.13 mmol) [N. C. Brown et al, J. Med. Chem., 42, 2035-2040 (1999)] and 3-iodo-4-methylaniline (47 mg, 0.20 mmol) [G. E. Wright et al., J. Med. Chem., 27, 181-185 (1984)] in 2- methoxyethanol (3 mL) / H₂O (1 mL) was heated at reflux for 12 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1₃ (2 x 10 mL) and dried (vacuum oven, 60°) to give 15 as a white powder. NMR: δ 0.81 (t, J7.3 Hz, 3 H), 1.48 (m, 2 H), 2.31 (s, 3 H), 3.65 (t, J 7.3 Hz, 2 H), 4.72 (s, 1 H), 7.12 (m, 1 H), 7.31 (d, J8.0 Hz, 1 H), 7.63 (s, 1 H), 8.18 (bs, 1 H), 10.6 (bs, 1 H). HPLC A: 2.75 min.

A mixture of 3-propyl-6-chlorouracil (25 mg, 0.13 mmol) [N. C.

Brown et al, J Med. Chem., 42, 2035-2040 (1999)] and 3,4-dichlorobenzylamine (69 mg, 0.39 mmol) in 2-methoxyethanol (1.5 mL) / H₂O (0.5 mL) was heated at reflux for 12 h. The reaction was diluted with H O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1₃ (2 x 10 mL) and dried (vacuum oven, 60°) to give 16 as a white powder. NMR: δ 0.78 (t, J7.3 Hz, 3 H), 1.44 (q, J7.3 Hz, 2 H), 3.58 (t, J7.3 Hz, 2 H), 4.28 (d, J 5.9 Hz, 2 H), 4.56 (s, 1 H), 6.66 (m, 1 H), 7.31 (d, J 8.0 Hz, 1 H), 7.57 (s, 1 H), 7.59 (d, J 8.0 Hz, 1 H), 10.21 (bs, 1 H). HPLC C: 2.59 min.

EXAMPLE 11

A mixture of 3-ethyl-6-chlorouracil (100 mg, 0.57 mmol) [N. C. Brown et al., J. Med. Chem., 42, 2035-2040 (1999)] and 3,4-dichlorobenzylamine (0.324 g, 1.84 mmol) in 2-methoxyethanol (6 mL) / H₂O (2 mL) was heated at reflux for 6 h. The reaction was diluted with H₂O (10 mL) and the product collected by filtration. The solid was washed with hot CHC1₃ (2 x 10 mL) and dried (vacuum oven, 60°) to afford 17 as a white powder. NMR (CDC1₃): δ 1.00 (t, J7.0 Hz, 3 H), 3.69 (q, J7.0 Hz, 2 H), 4.26 (d, J6.2 Hz, 2 H), 4.45 (s, 1 H), 6.69 (m, 1 H), 7.30 (dd, J8.2 and 2.1 Hz, 1 H), 7.57 (d, J 1.8 Hz, 1 H), 7.61 (d, J8.2 Hz, 1 H), 8.24 (bs, 1 H), 10.28 (bs, 1 H).

EXAMPLE 12

Step A:

Using the procedure in Example 1 , Step A N-cyclohexylurea was reacted with malonic acid to give N-cyclohexylbarbituric acid 18. ΝMR: δ 1.03-1.13 (m, 1 H), 1.18-1.29 (m, 2 H), 1.52-1.62 (m, 3 H), 1.71-1.78 (m, 2 H), 2.07-2.17 (m, 2 H), 3.56 (s, 1 H), 4.36-4.44 (m, 1 H), 11.17 (s, 1 H). Step B:

Using the procedure in Example 1 , Step B N-cyclohexylbarbituric acid 19 was reacted with phosphorus oxychloride to give 3-cyclohexyl-6-chlorouracil 19. ΝMR: δ 1.03-1.13 (m, 1 H), 1.18-1.29 (m, 2 H), 1.46-1.52 (m, 2 H), 1.55-1.62 (m, 1 H), 1.71-1.78 (m, 2 H), 2.19-2.28 (m, 2 H), 4.49-4.56 (m, 1 H), 5.8 (s, 1 H), 12.2 (bs, I H). HPLC C: 1.81 min.

Step C:

20

Using the procedure in Example 1, Step C 3-cyclohexyl-6-chlorouracil 20 was reacted with 3-iodo-4-methyl aniline to afford 20 as a light tan powder. ΝMR: δ 1.03-1.13 (m, 1 H), 1.18-1.29 (m, 2 H), 1.42-1.48 (m, 2 H), 1.55-1.61 (m, 1 H), 1.71-1.77 (m, 2 H), 2.23-2.32 (m, 2 H), 2.32 (s, 3 H), 4.51-4.58 (m, 1 H), 4.69 (s, 1 H), 7.14 (dd, J 8.15 and 2.3 Hz, 1 H), 7.29 (d, J 8.1 Hz, 1 H), 7.61 (d, J2.3 Hz, 1 H), 8.16 (s, 1 H), 10.4 (bs, 1 H). HPLC A: 3.31 min.

EXAMPLE 13

21

Using the procedure in Example 1, Step C 3-cyclohexyl-6-chlorouracil 20 was reacted with 3,4-dichlorobenzylamine to afford 21 as a yellow powder. NMR: δ 1.0-1.1 (m, 1 H), 1.15-1.28 (m, 2 H), 1.37-1.43 (m, 2 H), 1.55-1.59 (m, 1 H), 1.68- 1.74 (m, 2 H), 2.2-2.29 (m, 2 H), 4.26 (d, J6.2 Hz, 2 H), 4.46 (s, 1 H), 4.46-4.54 (m, 1 H), 6.61 (bm, 1 H), 7.29 (dd, J 8.2 and 1.8 Hz, 1 H), 7.58 (d, J 1.8 Hz, 1 H), 7.6 (d, J8.2 Hz, 1 H), 10.3 (bs, 1 H). HPLC C: 3.12min.

Biological Assays

Cloning, Expression, and Purification DNA polymerase HI (Pol HI) was cloned by PCR from S. aureus genomic DNA. The Pol HI gene was cloned into pETl 5. Poi m/pET15 was transformed into BL21 cells. The cells were grown at 29°C in M9ZB media containing ampicillin and chloramphenicol to an OD of 1.0. The cells were induced by adding 1 mM IPTG and grown for three hours. The cells were centrifuged at 2500 x g for 10 minutes. The cell pellet was resuspended in 50 mM Tris, pH 7.4, 0.1 % Triton XI 00, 1 mM EDTA, 20%> glycerol, and complete protease inhibitor cocktail (Boehringer Mannheim) and lysed by freeze/thawing three times in a dry ice and methanol bath. The lysate was centrifuged at 10,000 x g for one hour. The supernatant was loaded onto a HiTrapQ column that was equilibrated in 50 mM Tris, pH 7.4, 20% glycerol, and 1 mM EDTA. Following loading, the column was washed with 20 column volumes of buffer. The Pol IH was eluted using a linear NaCl gradient from 0-0.5 M. The Pol HI activity eluted between 0.3 and 0.4 M NaCl. The peak of activity was loaded onto a HiTrap Blue column equilibrated in 50 mM Tris, Ph 7.4, 20%) glycerol, lmM EDTA, and 1 mg/ml BSA. The column was washed with 10 column volumes of equilibration buffer, followed by a wash with 20 column volumes of equilibration buffer containing 0.5 M NaCl. The Pol HI was eluted by washing the column with equilibration buffer containing 3 M NaCl.

Inhibition Assay

The reaction mix consisted of 30 mM Tris HC1, pH 7.5, 20% glycerol, 4 mM DTT, 10 mM MgOAc, 0.003 mM dATP, 0.003 mM dGTP, 0.001 mM dCTP, 0.001 mM ³H-dTTP, and 0.35 mg/ml 'activated' calf thymus DNA (Worthington Enzymes) in a final volume of 0.1 ml. The assay was initiated by the addition of enzyme and incubated for 30 minutes at 30°C. The assay was stopped by the addition of cold 10%TCA/0.1%) NaPPi. The incorporation of ³H-dTTP into the calf thymus DNA was monitored by capturing the precipitated DNA onto a GF/C filter, followed by counting in a scintillation counter. The range of activity for the compounds of Formulas I and H in this assay were about 2 to about 25 μM.

PICA (DNA Polymerase HI Inhibition Whole-Cell-based Assay) Standard Operating

Procedures

Assay organism growth and storage conditions:

Five organisms were tested in the PICA assay. Specific conditions for the growth and storage of these cultures are provided in the table below. Standard microbiological techniques were used in the routine maintenance of the cultures.

Media Inoculum

Strain Species Long term Working slant Overnight MIC Purity Dilution storage broth assay plate

F2 B. subtilis LB slant room L LBB L LBB LB LB 1 to 100 temp

MB4926¹ E. coli envA Frozen vial B BHHII T TSSBB MH LB & LB+ 1 to 100

TSB rif¹

R A-1 E.faecium Frozen vial B BHHII TTSSBB BHI BHI 1 to 10

BHI

MB2865 S. aureus Frozen slant Thaw reedd ssllaanntt TTSSBB MH BHI 1 to 100

TSB TSB

MCL5350 S. Frozen slant Thawed slant TSB+ BHI Blood 1 to 10 pneumoniae BHI+10%HS BHI+10%HS 10%HS Agar ¹ This strain was replaced at the end of the program by a more sensitive strain (MB5746).

MLC assay:

Samples from were tested initially in three concentrations, 100 μM, 10 μM, and 1 μM final. Samples were resuspended at a concentration of 2 or 10 mM in DMSO (if required), then serial 10-fold dilutions of this stock were prepared to achieve the final concentrations indicated. Samples were diluted either by hand or using a Denley Wellpro liquid handling system (manufactured by Labsystems). Five μl of each concentration were transferred from the dilution plate to replica assay plates either by hand or using a Quadra-96 model 320 liquid handling device (manufactured by Tomtec). Media was added either by hand or using the Denley to a final assay volume of 100 μl to give a final DMSO concentration of 5%. DMSO was run as the vehicle control. Media used were specific for each strain as indicated in the table above. Assay plates were inoculated using an MIC-2000 (manufactured by Dynex Technologies) from cultures diluted into phosphate-buffered saline (made by Gibco-BRL)as indicated in the table above. Assay plates were incubated overnight at 37°C and then examined for the presence/absence of growth of the bacteria in the wells.

Results are expressed as the MLC, that is, the minimum log concentration that gives inhibition of the growth of the indicated organism (ie >100, 100, 10, and ^.). Any sample which was active on one or more strains was then tested in a more shallow dilution series to give a more specific measure of activity (see MIC below). The range of activity for the compounds of Formulas I and π in this assay were about 10 to about 100 μM.

MIC assay:

The procedures for the MIC assay were essentially as described above for the MLC assay, except that serial two-fold dilutions of the compounds were made from a final initial high concentration of 100 μM. In addition, the effect of serum albumin on the activity of the compounds was examined by testing MICs against the MB2865 strain in the presence and absence of a final 4.3 mg/ml concentration of human serum fraction V (Calbiochem). Results are expressed as the minimum inhibitory concentration (MIC); the lowest two-fold dilution which gives inhibition of growth (>100, 100, 50, 25, 12.5 etc., in μM). The range of activity for the compounds of Formulas I and II in this assay were about <0.5 to about 50 μM.

MOA assay:

Compounds which were active in the MIC assay were tested for the mode of action (MOA) by whole-cell dose-response labeling. Each compound was tested versus five different labeled precursors to investigate the effect on DNA synthesis (6- ³H Thymidine, 1 μCi/ml final, plus uridine at 50 μg/ml final concentration), RNA synthesis (5,6- ³H Uracil, 1 μCi/ml final), protein synthesis (4,5- H Leucine, 5 μCi/ml final), phospholipid synthesis (2-³H Glycerol, 1 μCi/ml final), and cell wall synthesis (2,3- ³H-alanine, 5 μCi/ml final, plus chloramphenicol at 100 μg/ml final). All labeled precursors were either from Amersham or New England Nuclear. In most cases MB2865 was the assay organism, but in cases where compounds had activity against the Bacillus strain and not MB2865, then that strain was used. Overnight cultures grown in Muller-Hinton medium were diluted 1 : 100 (3 ml) into 300 ml (pre- warmed) MH broth containing 50 μg/ml uridine,. incubated at 37°C with shaking to an OD of 0.1 (mid- log), and harvested by centrifugation. The cells were resuspended to an OD of 0.5 in pre- warmed MH medium.

Test and control compounds were serially diluted either two-fold or three- fold (depending on potency) in the appropriate diluent for the compound (water or DMSO) and then 5 μl of each transferred to each of five assay plates. A final assay volume of 100 μl also included precursor diluted into MH medium to obtain the final concentration indicated above and 70 μl of cells at OD 0.5. Addition of cells began the reaction allowed to proceed for 20 min. and stopped by addition of 50%> TCA to a final concentration of 10%. TCA precipitable counts were collected onto glass fiber filters (Wallac) using a Skatron Micro96 harvester. Filter mats were placed in bags with 10 ml scintillation fluid and loaded into cassettes for measurement in an LKB 1205 Betaplate counter (Wallac).

Results are expressed as the percentage of control counts (vehicle alone, no drug) present in each sample well plotted as a function of percent of control versus concentration of compound on a semi-log plot. The concentration of compound giving 50%> inhibition of each macromolecular synthesis (IC₅₀) is determined from this plot. The range of activity for the compounds of Formulas I and H in this assay were about 1.0 to about 25 μM.

Claims

WHAT IS CLAIMED IS:

1. A compound represented by formula I:

including pharmaceutically acceptable salts, stereoisomers or esters thereof, wherein:

Ri represents H, Ci-i o alkyl, C2-10 alkenyl, C2-10 alkynyl, (CH2)nC3-10 alicyclic, (CH2)_nC3-10 heterocyclic, (CH2)_nC5-10 aryl, (CH2)_nC5-lθheteroaryl,

(CH₂)_ndiaryl, (CH₂)_nOR , (CH₂)_mCO₂R², (CH₂)_nN(R2)₂, (CH₂)_nCON(R2)₂,

said alkyl, alkenyl, alkynyl, aryl, heteroaryl, optionally substituted with 1 to 3 groups of R^a; and providing that when R¹ is H, CH3, CH2CH3, CH2CH=CH2 or (CH2)2-5CH3, R3 cannot be 3,4-trimethyleneanilino or when R is H, CH3, CH2CH3, CH2CH-CH2 or (CH2)2-5CH3, R3 cannot be 3-ethyl-4-methylanilino;

m is 0 to 5; n is 0 to 5; p is 0 to 2;

R2 represents H, Ci-10 alkyl;

3 R is C3-1 oalicyclic, C3-i()heterocyclic, (CH2)nC5-10aryl,

(CH2)nC5-10 heteroaryl, NH(CH2)nC5-10aryl, or NH(CH2)nC5-lθheteroaryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R; R is H, Ci-6 alkyl, Ci-6 alkyl-OH, halo, Ci-6 alkylhalo, OR², CN, CF3, N(R²)2, CO2R², NO2, NHCOR², SO2R² or SR²;

R^a represents Ci-io alkyl, C3-8 cycloalkyl, halo, Ci -6 alkyl-OH, OH, Cl _6 alkylhalo, CF3, NH2, Ci-6 alkylNH₂, -SH, -SCι_-4alkyl, -CN, -COC,_-8alkyl, -Cs-io aryl, -COC_5-1o aryl, -C_5-1o heteroaryl, -COC₅-1₀ heteroaryl, Cι_-4alkyl-aryl, CONR⁶R⁷, NHCOR², OCOR⁶, -NR⁶(CO)R⁷, NR⁶(CO)NHR⁷, NHSO₂R⁶, OR⁶, CO₂R⁶, or NR⁶R^{7 and}

R⁶ & R⁷ independently represent H, Ci-8 alkyl, C3-8 cycloalkyl, or -

C_5-ιo aryl.

2. A compound in accordance with claim 1 wherein R represents Cι_-8 alkyl, C_2-8 alkenyl, (CH2)nC5-10 aryl, or (CH2)nC5-lθ alicyclic, said alkyl, alkenyl, aryl or alicyclic optionally substituted with 1-3 groups of R^a.

3

3. A compound in accordance with claim 1 wherein R C3-I oalicyclic,

(CH2)_nC5-10aryl, (CH2)_nC5-lθheteroaryl, or NH(CH2)_nC5-iθaryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R.

4. A compound in accordance with claim 1 wherein where R represents Cι_-8 alkyl, C_2-8 alkenyl, (CH2)_nC5-l0 aryl, or (CH2)nC5-lθ alicyclic, said alkyl, alkenyl, aryl or alicyclic optionally substituted with 1-3 groups of R^a; and R represents C3-I oalicyclic, (CH2)nC5-10aryl_? (CH2)nC5-lθheteroaryl, or NH(CH2)nC5-10aryl, said aryl or heteroaryl optionally substituted with 1 to 3 groups of R, optionally substituted with 1 to 3 groups of R.

5. A compound in accordance with claim 1 which is represented in Table TABLE 1

Table 1 Cont'd

6. A pharmaceutical composition comprised of a compound in accordance with claim 1 in combination with a pharmaceutically acceptable carrier.

7. A method of treating a bacterial infection comprising administering to a mammalian patient in need of such treatment a compound as defined in claim 1 in an amount which is effective for treating a bacterial infection.

8. A method of treating a bacterial infection involving methicillin resistant Staphylococcus aureus, methicillin resistant Staphylococcus epidermidis, B. subtilis, Enterococcus facalis/fecium, Streptococcus pneumomae, methicillin resistant coagulase negative Staphylococci microoganisms or any combination thereof comprising administering to a mammalian patient in need of such treatment a compound as defined in claim 1 in an amount which is effective for treating a bacterial infection.