AU2004200500A1 - IL-8 receptor antagonists - Google Patents

Description

11-02-'04 18:28 FROM-DCC +61392542770 T-632 P05/55 U-654

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT: SmithKline Beecham Corporation ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Nicholson Street Melbourne, 3000.

INVENTION TITLE: "IL-8 receptor antagonists" The following statement is a full description of this invention, including the best method of performing it known to us: COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:28 FROM-DCC +61392542770 T-632 P06/55 U-654 IL-8 RECEPTOR ANTAGONISTS This application is a divisional application of Australian Patent Application No. 58750/00, the contents of which are incorporated herein by reference.

FIELD OF THE INVENTION This invention relates to a novel group of phenyl urea compounds processes for the preparation thereof, the use thereof in treating IL-8, GROa. GROP, GROy,, NAP-2, and ENA-78 mediated diseases and pharmaceutical compositions for use in such therapy.

BACKGROUND OF THE INVENTION Many different names have been applied to Interlcukin-8 such as neutrophil attractantlactivation protein-I (NAP-1), monocyte derived neutrophil chemotactic factor (MDNCF), neutrophil activating factor (NAF), and T-cell lymphocyte chemotactic factor. Interleukin-8 is a chemoattractant for neutrophils, basophils, and a subset of T-cells. It is produced by a majority of nucleated cells including mnacrophages, fibroblasts, endothelial and epithelial cells exposed to TNF.

IL- laL- 10 or LPS, and by neutrophils themselves when exposed to LPS or chemotactic factors such as FMLP. M. Baggiolini et al, J. Clin. Invest. 84, 1045 (1989); J. Schroder et al, J. _Irrmunol. 139, 3474 (1987) and J. Immunol. 144, 2223 (1990) Stricter, et al, Science 243, 1467 (1989) and J. Biol. Chem. 264. 10621 (1989); Cassatella et al, J. Immunol. 148, 3216 (1992).

GROca, GROJ, GROy and NAP-2 also belong to the chemokine a family.

Like IL-8 these chemokines have also been referred to by different names. For instance GROa, 13, y have been referred to as MGSAc. 0 and yrespectively (Melanoma Growth Stimulating Activity), see Richmond et al, J. Cell Physiology 129, 375 (1986) and Chang et al, 1. Immunol 148, 451 (1992). All of the chemokines of the a-family which possess the ELR motif directly preceding the CXC motif bind to the IL-8 p receptor.

IL-8, GROa, GROp, GROy, NAP-2 and ENA-78 stimulate a number of functions in vitro. They have all been shown to have chemoattractant properties for neutrophils, while IL-8 and GROct have demonstrated T-lymphocytes, and basophiles chemotactic activity. In addition IL-8 can induce histamine release from 1- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:28 FROM-DCC +61392542770 T-632 P07/55 U-654 basophils from both normal and atopic individuals GROa and IL-8 can in addition, induce lysozomal enzyme release and respiratory burst from neutrophils. IL-8 has also beon shown to increase the surface expression of Mac-1 (CD1 lb/CD18) on neutrophils without dc novo protein synthesis. This may contribute to increased adhesion of the neutrophils to vascular endothelial cells. Many known diseases are characterized by massive neutrophil infiltration. As IL-8, GRO GROR, GROy and NAP-2 promote the accumulation and activation of neutrophils, these chemokines have been implicated in a wide range of acute and chronic inflammatory disorders including psoriasis and rheumatoid arthritis, Baggiolini et al, FEBS Lett. 307, 97 (1992); Miller et al, Crit. Rev. ImmunoL 12, 17 (1992); Oppenheim et al, Annu.

Rev. Immunol. 9, 617 (1991); Seitz et al., J. in. Invest. 87.463 (1991); Miller et al., Am. Rev. Respir. Dis. 14, 427 (1992); Donnely et al., Lancet 341, 643 (1993).

In addition the ELR chemokines (those containing the amino acids ELR motif just prior to the CXC motif) have also been implicated in angiostasis. Stricter et al., Science 258, 1798 (1992).

In vitro, IL-8, GROc, GROI, GROy, and NAP-2 induce neutrophil shape change, chemotaxis, granule release, and respiratory burst, by binding to and activating receptors of the seven-transmembrane, G-protein-linked family, in particular by binding to IL-8 receptors, most notably the p-receptor. Thomas et al., J. Biol. Cher. 266. 14839 (1991); and Holmes et al., Science 253, 1278 (1991). The development of non-peptide small molecule antagonists for members of this receptor family has precedent. For a review see R. Freidinger in: Progress in rugr Research, Vol. 40, pp. 33-98, Birkhauser Verlag, Basel 1993. Hence, the IL-8 receptor represents, a promising target for the development of novel anti-inflammatory agents.

Two high affinity human IL-8 receptors (77% homology) have been characterized: IL-SRo, which binds only IL-8 with high affinity, and IL-8RP, which has high affinity for IL-8 as well as for GROa, GROp, GROy and NAP-2. See Holmes et al., supra; Murphy et al., Science 253, 1280 (1991); Lee et al., J. Biol.

Chem. 267, 16283 (1992): LaRosa et al., J. Biol. Chem. 267. 25402 (1992); and Gayle et al., J. BioL Chem. 268, 7283 (1993).

-2- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:28 FROM-DCC +61392542770 T-632 P08/55 U-654 There remains a need for treatment, in this field, for compounds which are capable of binding to the IL-8 a or j3 receptor. Therefore, conditions associated with an increase in IL-8 production (which is responsible for chemotaxis of neutrophil and T-cells subsets into the inflammatory site) would benefit by compounds which are inhibitors of IL-8 receptor binding.

SUMMARY OF THE INVENTION This invention provides for a method of treating a chemokine mediated disease, wherein the chemokine is one which binds to an IL-8 a or A receptor and which method comprises administering an effective amount of a compound of Formula or a pharmaceutically acceptable salt thereof. In particular the chemokine is IL-8.

This invention also relates to a method of inhibiting the binding of IL-8 to its receptors in a mammal in need thereof which comprises administering to said mammal an effective amount of a compound of Formula Compounds of Formula useful in the present invention are represented by the structure:

X

W-N N-(CRR, 1 )v -R wherein X is oxygen or sulfur; R is (CRgRg)r C(0) 2 R, (CRgR 8 )r NH-C(O)Ra, (CRgRg)r C(O)NR6'R7', (CR8R8)rNHS(0)2Rb, (CR8Rg)r S(0)2NHRc, (CRgRg)r NHC(X2)NHRb, or a tetrazolyl ring; X2 is oxygen or sulfur; RI is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted alkyl; CI-10 alkyl; C2-10 alkenyl; CI-10 alkoxy; halosubstituted alkoxy; azide; (CRgRg)q S(O)tR 4 hydroxy; bydroxy Cl-4alkyl; aryl; aryl C1-4 -3- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:29 FROM-DCC +61392542770 T-632 P09/55 U-654 alkyl; aryloxy; aryl C 1-4 alkyloxy; heteroaryl; heteroarylalkyl; heterocyclic, heterocyclic CI-4alkyl; heteroaryl Ci-4 alkyloxy; aryl C2-10 alkenyl; heteroaryl C2-10 alkenyl; heterocyclic C2-10 alkenyl; (CRgR8)qNR4R5; C2-10 alkenyl

(CR

8

R

8 )q C(O)NR4R5; (CR 8

R

8 )q C(O)NR4RIO; S(0)3Rg; S (CRgR8)q C(O)RI 1; C2-10 alkenyl C(O)RI 1; C2-10 alkenyl C(O)ORi I(CR 8 Rg)q C(0)ORI2; (CRgRg)q OC(O) RI l; (CRgR8)qNR4C(O)Rl 1; (CRSgR)q NHS(0) 2 R17; (CRgRg)q S(0) 2

NR

4

R

5 or two RI moieties together may fonn O-(CH12)so- or a 5 to 6 membered saturated or unsaturated ring; and wherein the aryl. hetcroaryl, and heterocyclic containing moieties may be optionally substituted; provided that there is no ionizable hydrogen having a pKa of 3 to 10 in the 2-position of the phenyl ring; n is an integer having a value of 1 to 3; m is an integer having a value of I to 3; q is 0, or an integer having a value of 1 to r is 0 or an integer of 1 to 4; s is an integer having a value of 1 to 3; t is 0, or an integer having a value of I or 2; v is an integer having a value of 1 to 4; R4 and R5 are independently hydrogen, optionally substituted C1-4 alkyl, optionally substituted aryl, optionally substituted aryl Cl-4alkyl, optionally substituted heteroaryl. optionally substituted heteroaryl C I-4alkyl, heterocyclic, heterocyclic CI-4 alkyl, or R4 and R5 together with the nitrogen to which they are attached form a 5 to 7 member ring which may optionally comprise an additional heteroatom selected from O/N/S; R6 and R7 are independently hydrogen or a C 1-4 alkyl group, or R6 and R7 together with the nitrogen to which they are attached form a 5 to 7 member ring which ring may optionally contain an additional heteroatom which heteroatom is selected from oxygen, nitrogen or sulfur; -4- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:29 FROM-DCC +61392542770 T-632 P10/55 U-654 R6' and R- ware independently hydrogen. CI-4 alkyl, aryl, arylC -4alkyl, arylC2-4alkenyl, heteroaryl, heteroarylC.4alkyl, heteroarylC2-4 alkenyl.

heterocyclic, heterocyclic C1-4alkyl, beterocyclic C2-4alkenyl moiety, provided that one of R6' and R7' is a hydrogen, but not both; Y is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted alkyl; Cl-10 alkyl; C2-10 alkenyl; C1-10 alkoxy; halosubstituted alkoxy; azide; (CR 8

R

8 )q S(0)tR4; hydroxy; hydroxyCl-4alkyl; aryl; aryl CI4 alkyl; aryloxy; arylCl-4 alkyloxy; heteroaryl; heteroarylalkyl; heteroaryl C-4 alkyloxy; heterocyclic, heterocyclic C-4alkyl; aryl C2-10 alkenyl; heteroaryl C2-10 alkenyl; heterocyclic C2-10 alkenyl; (CRgRg)q NR4R5;.C2-10 alkenyl (CRgR 8 )q C(O)NR4R5; (CRgR8)q C(O)NR4RIO; S(O)3R8; (CR8Rg)q C(O)R11; C2-10 alkenyl C(O)R11; .C2-10 alkenyl C(O)OR 1; C(O)R 1; (CRgRg)q C(0)OR12; (CRgRg)q OC(O) Rj 1; (CRgR 8 )qNR4C(O)Rl 1; (CRgRg)q NHS(0)2Rd; (CR8Rs)q 5(0)2NR4R5; or two Y moieties together may form O-(CH2)sO- or a 5 to 6 membered saturated or unsaturated ring; and wherein the aryl, heteroaryl, and heterocyclic containing moieties may be optionally substituted; Rg is independently selected from hydrogen or C1-4 alkyl; RIO is Cio10 alkyl C(0)2R8; R11 is hydrogen, C1-4 alkyl, optionally substituted aryl, optionally substituted aryl C 1-4alkyl, optionally substituted heteroaryl, optionally substituted heteroarylC 1-4alkyl, optionally substituted heterocyclic, or optionally substituted heterocyclicCi-4alkyl; R12 is hydrogen, C I-10 alkyl, optionally substituted aryl or optionally substituted arylalkyl; Rl3 and R14 are independently hydrogen, optionally substituted C1-4 alkyl, or one of Rl3 and R14 may be optionally substituted aryl; COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:29 FROM-DCC +61392542770 T-632 P11/55 U-654 R17 is Ci-4alkyl, aryl, arylalkyl, heteroaryl, heteroarylCl14alkyl, heterocyclic, or hezcrocyclicC1-4alkyl, wherein the aryl, heteroaryl and heterocyclic rings may all be optionally substituted; Ra is an alkyl, aryl, azyl Cl-4alkyl, heteroaryl, beteroaryl Cj4alkyl. heterocyclic, or a heterocyclic Ci -4alkyl moiety, wherein all of these moieties may be optionally substituted; Rb is a NR6R7, alkyl, aryl, arylCl4alkyL, arylC2-4alkenyl, heteroaryl, heteroarylCl-4alkyl, heteroarylC2.4 alkenyl, heterocyclic, heterocyclic Cj.4ialkyl, heterocyclic C 2 -4alkenyl moiety, or camphor, wherein all of these moieties may be optionally substituted; Re is alkyl. aryl, arylC14alkyl, arylC2-4alkenyl, heteroaryl, heteroaryIC14alkyl, heteroarylC2-4alkeuyl, heterocyclic, heterocyclic C 1-4alkyl, or a heterocyclic C2-4alkenyl moiety, wherein all of thesc moieties may be optionally substituted; Rd is NR6R 7 ,'alkyl, ary1C1-4 alkyl. aTyIC 2-4 alkenyl, beteroaryl, heteroaryl-Cj-4alkyl, heteroarylC 2 -4 alkenyl, heterocyclic, beterocyclicC 1 4 alkyl, wherein the aryl, beteroaryl and heterocyclic containing rings may be optionally substituted;

R

(R)m W is ,or the E containing ring is optionally selected from 0 s

(R

1 )m

R,

0 0 1 or Ri ;the asterix 'Sdenoting point of attachment of the ring: and -6- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:30 FROM-DCC +61392542770 T-632 P12/55 U-654

R

2 0 is WI, optionally substituted heteroaryl, optionally substituted C 5 8 cycloalkyl, optionally substituted C1-10 alkyl, optionally substituted C 2 10 alkenyl, or an optionally substituted C 2 10 alkynyl; Y)n Wi is K.E ,or S the E' containing ring is optionally selected from 0 8 0o n(Y) :or (Y) the asterix denoting point of attachment of the ring; or a pharmaceutically acceptable salt thereof.

DETAILED DESCRIPTION OF THE INVENTION The compounds of Formula may also be used in association with the veterinary treatment of mammals, other than humans, in need of inhibition of IL-8 or other chemokines which bind to the IL-8a and P receptors. Chemokine mediated diseases for treatment, therapeutically or prophylactically, in animals include disease states such as those noted herein in the Methods of Treatment section.

In compounds of Formula R is (CRgR 8 )r C(0)2H, (CRgRg)r NH-C(O)Ra,

(CR

8 Rg)r C(O)NR6R7', (CRSRB)rNHS(0)2Rb, (CRgRg)r S(0)2NHRc, (CRgR 8 )r NHC(X2)NHRb, or a tetrazolyl ring. Each of these moieties may be directly attached to the ring in the 3-position or through the linker (CRgRg)r to the 3-position of the ring.

Suitably, r is 0 or an integer of I to 4, preferably 0.

Suitably, X2 is oxygen or sulfur, preferably oxygen, wherein r is 0 or an integer having a value of I to 4.

7.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:30 FROM-DCC +61392542770 T-632 P13/55 U-654 Suitably, R6 and R7 are independently hydrogen or a C 1-4 alkyl group, or R6 and R7 together with the nitrogen to which they are attached form a 5 to 7 member ring which ring may optionally contain an additional heteroatom which heteroatom is selected from oxygen, nitrogen or sulfur.

Suitably, R6' and R7' are hydrogen, CI)4 alkyl, aryl, arylC l-4alkyl, arylC24alkenyl, heteroaryl, heteroarylC 1-4alkyl, beteroarylC2-4 alkenyl, heterocyclic, beterocyclic C1-4alkyl, or a heterocyclic C2-4alkenyl moiety- provided that one of R6' and R7' are hydrogen, but not both of R6,' and R7: All of these moieties may be optionally substituted one to three times independently by halogen; io nitro; halosubstituted C1-4 alkyl, such as CF3; C1-4 alkyl, such as methyl; Ci-4 alkoxy, such as methoxy; NRgC(O)Ra; C(O)NR 6

R

7 S(0)3H; or C(0)OCl-4 alkyl.

Suitably Ra is an alkyl, aryl, arylC -4alkyl, heteroaryl, heteroarylCI-4alkyl, heterocyclic, or a heterocyclic Cj -4alkyl moiety, wherein all of these moieties may be optionally substituted as defined herein.

Suitably, Rb is a NR6R7, alkyi, aryl, arylCI-4alkyl, arylC2-4alkenyl, heteroaryl, heteroarylCi-4alkyl, heteroarylC2-4 alkenyl, heterocyclic, heterocyclic CI-4alkcyl, or a heterocyclic C2-4alkenyl moiety, or camphor, wherein the alkyl, aryl, beteroaryl and heterocyclic containing moieties may all be optionally substituted one to three times independently by halogen; nitro; halosubstituted C1-4 alkyl, such as CF3; C1-4 alkyl, such as methyl; C1-4 alkoxy, such as methoxy; NR9C(O)Ra; C(O)NR6R7; S(0)3H; orC(0)OCi-4 alkyl. Rb is preferably an optionally substituted phenyl, benzyl, or styryl. When Rb is a heteroaryl ring, it is preferably an optionally substituted thiazole, an optionally substituted thienyl, or an optionally substituted quinolinyl ring.

Suitably, R9 is hydrogen or a C 1-4 alkyl group, preferably a hydrogen.

When R9 is in the substituent group NR9C(O)Ra, then Ra is preferably an alkyl group, such as methyl.

-8- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:30 FROM-DCC +61392542770 T-632 P14/55 U-654 Suitably Rc is hydrogen, alkyl, aryl, arylCi-4alkyl, arylCj.4alkenyl, heteroaryl, heteroarylC 1 -4alkyl, heteroarylC 1 -4alkenyl, heterocyclic, or heterocyclic C14alkyl, or a heterocyclic C -4alkenyl moiety, all of which may be optionally substituted one to three times independently by halogen, nitro, halosubstituted C I-4 alkyl, C1-4 alkyl, C1-4 alkoxy, NRgC(O)Ra, C(O)NR6R7. S(0)3H, or C(O)OC1-4 alkyl. Preferably, Rc is an optionally substituted phenyL

R

O(RM)m Suitably, W is or Suitably, the E containing ring is an optionally substituent which is selected from 0 O0, R "I or R1 wherein the asterix denotes the point of attachment of the ring.

In compounds of Formula suitably RI is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted CI-10 alkyl, such as CF3; alkyl, such as methyl, ethyl, isopropyl, or n-propyl; C2-10 alkenyl; C -10 alkoxy, such as methoxy, or ethoxy; halosubstituted C1-10 alkoxy, such as trifluoromethoxy; azide; (CRgR 8 )q S(O)tR4; hydroxy; hydroxy C l4alkyl, such as methanol or ethanol; aryl,. such as phenyl or naphthyl; aryl Ci-4 alkyl, such as benzyl; aryloxy, such as phenoxy; aryl Cl-4 alkyloxy. such as benzyloxy; heteroaryl; beteroarylalkyl; heteroaryl C1-4 alkyloxy; aryl C2-10 alkenyl; heteroaryl C 2 10 alkenyl: heterocyclic 9- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:30 FROM-DCC +61392542770 T-632 P15/55 U-654 C2-10 alkenyl; (CRsR8)qNR4RS; C2-10 alkenyl C(O)NR4R5; (CRgRg)q C(O)NR4RS; (CRgRg)q C(0)NR4R10; S(0)3Rg such as S(0)3H; (CRgRg)q C(O)RI 1; C2-10 alkenyl C(O)RI 1; C2-10 alkenyl C(O)OR I; C(O)Rj1; (CR 8 Rg)q C(O)ORI2; (CRgRg)qOC(O)Ri i; (CRgRg)q NR4C(0)R 11; (CRgR8)q NHS(0)2RI7; (CRgRS)qS(0) 2 NR4R5; or two RI moieties together may form O-(CH2)sO- or a 5 to 6 membered saturated or unsaturated ring. The aryl, heteroaryl, and heterocyclic containing moieties may all be optionally substituted as defined herein below.

Suitable, t is 0, an integer having a value of 1 or 2.

Suitably, s is an integer having a value of 1 to 3.

Suitably, q is 0, or an integer having a value of I to When RI forms a dioxybridge, s is preferably 1. When RI forms an additional saturated or unsaturated ring, it is preferably a 6 membered ring resulting in a naphthylene ring system. These saturated and unsaturated ring systems may be optionally substituted independently, 1 to 3 times by the other RI moieties as defined above.

Suitably, R4 and RS are independently hydrogen, optionally substituted C1.-4 Alkyl, optionally substituted aryl, optionally substituted aryl C1-4alkyl, optionally substituted heteroaryl, optionally substituted heteroaryl C l.4alkyl, heterocyclic, or heterocyclicC 1-4 alkyl, or R4 and RS together with the nitrogen to which they are attached form a 5 to 7 member ring which may optionally comprise an additional heteroatom selected from O/N/S.

Rg is suitably independently selected from hydrogen or C 1-4 alkyL- RIO is suitably C1-10 alkyl C(0)2R8, such as CH2C(0)2H or CH2C(0)2CH3.

RII is suitably independently hydrogen, C1-4 alkyl, aryl, aryl CI-4 alkyl, heteroaryl, hbeteroaryl Cl-4alkyl, heterocyclic, or heterocyclic C1-4alkyl.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:31 FROM-DCC +61392542770 T-632 P16/55 U-654 R12 is suitably hydrogen, Cl-10 alkyl, optionally substituted aryl or optionally substituted arylalkyl.

R17 is suitably C1-4alkyl, aryl, arylalkyl, heteroaryl, heteroarylCj-4alkyl, heterocyclic, or heterocyclicC-.4alkyl, wherein the aryl, heteroaryl and heterocyclic rings may all be optionally substituted, Preferably RI is halogen, cyano, nitro, CF3, C(Q)NR 4 R5, alkeny] C(O) R4RI0, alkenyl C(0)OR12, heteroaryl, heteroarylalkyl, heteroaryl alkenyl, or S(O)NR4R5, and preferably R4 and R5 are both hydrogen or one of R4 and R5 is phenyl, A preferred ring substitution for the RI group is in the 4-position of the phenyl ring.

When R is (CRsgRg) OH, (CR8R8)r SH or (CRsgR)r NHS(0)2Rb than R I is preferably substituted in the 4- position, or disubstituted in the 2,4-position.

Preferably, the RI substituent group is an electron withdrawing moiety, such as nitro, halogen, cyano, trifluoromethyl, or When R is a carboxylic acid, than RI is preferably hydrogen, or RI is preferably substituted in the 4-position, more preferably substituted by trifluoromethyl or chloro.

In compounds of Formula suitably R13 and RI4 are independently hydrogen, an optionally substituted Ci-4 alkyl which may be straight or branched as defined herein, or one of RI3 and R14 is an optionally substituted aryl.

When R 1 3 or R 14 are an optionally substituted alkyl, the alkyl moiety may be substituted one to three times independently by halogen; halosubstituted C1-4 alkyl such as trifluoromethyl; hydroxy; hydroxy C -4alkyl, C1-4 alkoxy; such as methoxy, or ethoxy; halosubstituted CI-10 alkoxy; S(0)tR4; aryl; NHC(O)R4; C(O)NR4R5; or C(O)ORg.

Suitably, v is 0 or an integer having a value of I to 4.

Suitably, Y is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted C-10io alkyl; C1-10 alkyl; C2-10 alkenyl; CI-10 alkoxy; -11- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:31 FROM-DCC +61392542770 T-632 P17/55 U-654 halosubstituted CI-10 alkoxy; azide; (CRgRg)q S(O)tR4; hydroxy; hydroxyC 1-4alkyl; aryl; aryl Cl-4 alkyl; aryloxy; arylC -4 alkyloxy; heteroaryl; heteroarylalkyl; heteroaryl Ci-4 alkyloxy; heterocyclic, heterocyclic C -4alkyl; aryl C2-10 alkenyl; heteroaryl C2-10 alkenyl; heterocyclic C2-10 alkenyl; (CRgRg)q NR4R5; C2-10 alkenyl C(O)NR4R5; (CR 8 Rg)q C(O)NR4R5; (CR 8 Rg)q C(O)NR4RIO; S(0)3H; S(0)3R8., such as S(0)3H; (CR8Rg)q C(O)RI 1; C2-10 alkenyl C(O)RI 1; C2-10 alkcnyl C(O)ORl 1; (CR g

R

8 g)q C(0)ORI2; (CR 8 R)q OC(O) R11: (CRgRg)q NR4C(O)R 1l; (CRgRg)q NHS(0)2Rd; (CR 8 Rg)q S(0) 2

NR

4 R5 or two Y moieties together may form O-(CH2)sO- or a 5 to 6 membered saturated or unsaturated ring. The aryl, heteroaryl, and heterocyclic containing moieties may all be optionally substituted, When Y fornms a dioxybridge, s is preferably 1. When Y forms an additional unsaturated ring, it is preferably 6 membered resulting in a naphthylene ring system.

These saturated and unsaturated rings may be optionally substituted 1 to 3 times by the other Y moieties as defined above.

Suitably, R d is a NR 6

R

7 alkyl, aryl C 1 .4 alkyl, arylC 2-4 alkenyl, heteroaryl, heteroaryl-C 1-4alkyl, heteroarylC2-4 alkenyl, heterocyclic.

heterocyclicC 1-4 alkyl, or heterocyclic C 2-4 alkenyl moiety, wherein the aryl, heteroaryl, and heterocyclic containing moieties may all be optionally substituted as defined herein.

Y is preferably a halogen, C 1-4 alkoxy, optionally substituted aryl, optionally substituted aryloxy or arylalkoxy, methylene dioxy, NR4R5, thio C 14alkyl, thioaryl, halosubstituted alkoxy, optionally substituted C -4 alkyl, or hydroxy alkyl. Y is more preferably a mono-substituted halogen, disubstituted halogen, mono-substituted alkoxy, disubstituted alkoxy, methylenedioxy, aryl, or alkyl. More preferably these groups are mono or di-substituted in the position or 3'-position of the phenyl ring.

12- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:31 FROM-DCC +61392542770 T-632 P18/55 U-654 While Y may be substituted in any of the 5 ring positions, preferably when R is (CRsRS)rC(0)2H, Y is preferably mono-substituted in the 2'-position or 3'-position. with the preferably being unsubstituted. If the ring is disubstituted, when R is (CR8Rg)rC(0) 2 H, substituents are preferably in the 2' or 3'position of a monocyclic ring. While both R 1 and Y can both be hydrogen, it is preferred that at least one of the rings be substituted, and more preferably that both rings are substituted.

In compounds of Formula X is suitably oxygen or sulfur, preferably oxygen.

The E and EF rings, denoted by its point of attachment through the asterix may optionally be present. If it is not present the ring is a phenyl moiety which is substituted by the RI and Y terms as shown herein. The E and E' ring may be substituted by the R and Y moiety, respectively, in any ring, saturated or unsaturated, and is shown for purposes herein substituted only in the unsaturated ring(s).

In compounds of Formula R20 is W 1 an optionally substituted beteroaryl, an optionally substituted C5.8 cycloalkyl, an optionally substituted C-10 alkyl, an optionally substituted C2- 10 alkenyl, or an optionally substituted C2.

10 alkynyl.

When R 2 0 is an optionally substituted C 5 .8 cycloalkyl ring, the ring may be substituted by (Y)n as defined above.

When R20 is an optionally substituted C i10 alkyl, an optionally substituted

C

2 .10 alkenyl, or an optionally substituted C 2 10 alkynyl, these moieties may be optionally substituted one or more times independently by halogen; nitro; cyano; halosubstituted C I-10 alkyl, such as trifluoromcthyl; C1-10i alkoxy; halosubstituted Ci-10 alkoxy; S(O)tR4; hydroxy; hydroxy C1-4alkyl;; aryloxy; arylCl-4 alkyloxy; heteroaryloxy; beteroaryl C1- 4 alkyloxy; heterocyclic, heterocyclic Cl-4alkyl; heterocyclicoxy; heterocyclic CI- 4 alkyloxy; NR4R5; C(O)NR4RS; C(O)NR4RIO; S(0)3H; S(0)3R8; C(O)Rl 1; C(0)OR12; OC(O)R1l; or NR4C(O)Rl1.

-13- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:31 FROM-DCC +61392542770 T-632 P19/55 U-654 When R 2 0 is an optionally substituted C 2 10 alkenyl, or an optionally substituted C 2 10 alkynyl these moieties may also, in addition to those moieties noted above, be optionally substituted with aryl, aryl CI-4 alkyl, heteroaryl, or a heteroaryl C -4 alkyl (and wherein these aryl and heteroaryl containing rings may be optionally substituted).

Yn Suitably. W 1 is or Suitably, the E' containing ring is optionally selected from 0 S.(Y)n o .o n(Y) Qn* n(Y n(Y) or In compounds of Formula when R20 is a beteroaryl (HET) ring, it is suitably a heteroaryl ring or ring system. If the HET moiety is a multi-ring system, the ring containing the heteroatom does not need to be directly attached to the urea moiety or the (CR 3 R14)v term- All the rings in this ring system may be optionally substituted by the term as defined above. Preferably, the HET moiety is a pyridyl, which may be 3- or 4-pyridyL If the ring is a multi system ring it is preferably a benzimidazole, dibenzothiophene, or indole ring. Other heterocyclic rings of interest include, but are not limited to thiophene, furan, pyrimidine, pyrrole, .14- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:32 FROM-DCC +61392542770 T-632 P20/55 U-654 pyrazole, quinoline, isoquinoline, quinazolinyl, pyridine, oxazole, thiazole, thiadiazole, triazole, or imidazole.

R2 is preferably an optionally substituted phenyl, allyl, CjI- 10 alkyl, ethoxy carbonyl ethyl, dimethylacetal, 2-methoxy isopropyl, or 2-methoxy ethyl group.

Exemplified compounds of Formula include: N-(3-Carboxypbenyl)-N'-(2-bromnphenyl)urea N-(3-Carboxymethylphenyl)-N'-(2-bromopbenyl)urea N-(3-Carboxymethylphenyl)-N'-(2,3-dichlorophenyl)urea N-(3-Carboxypbenyl)-N'-(2,3-dichlorophenyl)urea 1o N-[3-(2-Carboxyethyl)phenyl]-N-(2,3-dichlorophenyl) urea N-(2,4-Dichloro-3-carboxy)-N'-(2-bromophenyl) urea N-(4-Chloro-3-carboxyphenyl)-N'-(2-bromophenyl)urea N-(4-Chloro-3-carboxyphenyl) N'-(2,3-dichlorophenyl) urea; and N-(4-Chloro-3-carboxyphenyl)-N-(3-chlorophenyl)urea is or a pharmaceutically acceptable salt thereof.

As used herein, "optionally substituted" unless specifically defined shall mean such groups as halogen, such as fluorine, chlorine, bromine or iodine; hydroxy: hydroxy substituted C1-1oalkyl; CI-10 alkoxy, such as methoxy or ethoxy;

S(

0 C1.10 alkyl, wherein m'Is 0, 1 or 2, such as methyl thio, methyl sulfinyl or methyl sulfonyl; amino, mono di-substituted amino, such as in the NR4R5 group; NHC(O)R4; C(0)NR4R5; C(O)OH; S(0)2NR4R5; NHS(0)2R2, CI-1o alkyl. such as methyl, ethyl, propyl, isopropyl, or t-butyl; halosubstituted CI-10 alkyl, such CF3; an optionally substituted aryl, such as phenyl, or an optionally substituted arylalkyl, such as benzyl or phenethyl, optionally substituted heteracylic, optionally substituted heterocylicalkyl. optionally substituted heteroaryl, optionally substituted heteroaryl alkyl, and wherein these aryl heteroaryl, or heterocyclic moieties may be substituted one to two times by halogen; hydroxy; hydroxy substituted alkyl; Cl-o alkoxy; S(O)mCI-10 alkyl; amino, mono di- C1-4 alkyl substituted amino, such as in the NR4R5 group; CI-10 alkyl, or halosubstituted Cl.1o alkyl, such as CF3.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-' 04 18:32 FROM-DCC +61392542770 T-632 P21/55 U-654 R2 is suitably Cl -4 alkyl, aryl, aryl Ci-4alkyl, beteroaryl, beteroaryl- C1-4alkyl, heterocyclic, or heterocyclicCI-4alkyl.

Suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, sulphuric acid, phosphoric acid, methane sulphonic acid, ethane sulphonic acid, acetic acid, malic acid, tartaric acid, citric acid, lactic acid, oxalic acid, succinic acid, fumaric acid, maleic acid, benzoic acid, salicylic acid, phcnylacetic acid and mandelic acid. In addition, pharmaceutically acceptable salts of compounds of Formula may also be formed with a pharmaceutically acceptable cation, for instance, if a substituent group comprises a carboxy moiety.

Suitable pharmaceutically acceptable cations are well known to those skilled in the art and include alkaline, alkaline earth, ammonium and quaternary ammonium cations.

The following terms, as used herein, refer to: "halo" all halogens, that is chloro, fluoro, bromo and iodo.

"Cl-1oalkyl" or "alkyl" both straight and branched chain radicals of 1 to carbon atoms, unless the chain length is otherwise limited, including, but not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tertbutyl, n-pentyl and the like.

"cycloalkyl" is used herein to mean cyclic radicals, preferably of 3 to 8 carbons, including but not limited to cyclopropyl, cyclopentyl, cyclohexyl, and the like.

"alkenyl" is used herein at all occurrences to mean straight or branched chain radical of 2-10 carbon atoms, unless the chain length is limited thereto.

including, but not limited to ethenyl, 1-propenyl, 2-propenyl, 2-methyl-l-propenyl.

1-butenyl. 2-butenyl and the like.

"aryl" phenyl and naphthyl; "heteroaryl" (on its own or in any combination, such as "heteroaryloxy", or "heteroaryl alkyl") a 5-10 membered aromatic ring system in which one or more rings contain one or more heteroatoms selected from the group consisting of N, 0 or -16- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:32 FROM-DCC +61392542770 T-632 P22/55 U-654 S, such as, but not limited, to pyrrole, pyrazole, furan, thiophene, quinoline, isoquinoline, quinazolinyl, pyridine. pynrimidine, oxazole, thiazole, thiadiazole, triazole, imidazolc, or benzimidazole.

"beterocyclic" (on its own or in any combination, such as "heterocyclicalkyl") a saturated or partially unsaturated 4-10 membered ring system in which one or more rings contain one or more heteroatoms selected from the group consisting of N, O, or S; such as, but not limited to, pyrrolidine, piperidine, piperazine, morpholine, tetrahydropyran, or imidazolidine.

"arylalkyl" or "heteroarylalkyl" or "heterocyclicalkyl" is used herein to mean C 10 allcyl, as defined above, attached to an aryl. heteroaryl or heterocyclic moiety, as also defined herein, unless otherwise indicated, "sulfinyl" the oxide S of the corresponding sulfide, the term "thio" refers to the sulfide, and the term "sulfonyl" refers to the fully oxidized 5(0)2 moiety.

1 5 the term "wherein two RI moieties (or two Y moieties) may together form a 5 or 6 membered saturated or unsaturated ring" is used herein to mean the formation of a napthylene ring system or a phenyl moiety having attached a 6 membered partially unsaturated ring such as a C6 cycloalkenyl, i.e. hexene, or a cycloalkenyl moiety, such as a cyclopentene ring.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgmnent or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

-17- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:32 FROM-DCC +61392542770 T-632 P23/55 U-654 rO PFW i',47*W I ZZlS cl.it2,j METHODS OF PREPARATION The compounds of Formula may be obtained by applying synthetic procedures, some of which, are illustrated in the Schemes below. The synthesis provided for in these Schemes is applicable for the producing compounds of Formula having a variety of different R, R I, and aryl groups which are reacted, employing optional substituents which are suitably protected, to achieve compatibility with the reactions outlined herein- Subsequent deprotection, in those cases, then affords compounds of the nature generally disclosed. Once the urea nucleus has been established, further compounds of these formulas may be prepared 10 by applying standard techniques for functional group interconversion, well known in 17A- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:33 FROM-DCC +61392542770 T-632 P24/55 U-654 the art. While the schemes are shown with W and R 2 0 as phenyl this is merely for illustration purposes only.

The desired aniline 2-scheme-1 can be synthesized by the reduction of the corresponding nitro if it is not available commercially. This reduction can be accomplished by a number of reducing agents such as hydrogen and catalytic Palladium on carbon or tin chloride in a polar solvent such as DMF or ethyl acetate.

This aniline (2-scheme 1) can then be condensed with a commercially available isocyanate in an aprotic solvent such as DMF, DMSO or toluene.

Scheme I a N fb N 0 H H 0 I z a R=CH2CH 2 COOH, COOH, CH 2

COOH

a)H 2 Pd/C b)PhCNO Alternately, the desired compound could synthesized by the protection of the carboxylic acid by conditions well known in art, such as diazomethane to form the methyl ester. This compound could then be reduced by a number of reducing agents such as hydrogen and catalytic Palladium on carbon or tin chloride in a polar solvent such as DMF or ethyl acetate. Condensation with a phosgene equivalent such as dior triphosgene in the presence of a base such as triethyl amine or bicarbonate would form the isocyanate 4-scheme-2. This compound could then be reacted with the desired commercially available aniline. The carboxylic acid could then be deprotected by conditions standard in the art, such as metal hydroxide in a polar solvent such as THF/water, then acidified with an acid such as HCI to form 3, scheme 2.

18- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:33 FROM-DCC -61392542770 T-632 P25/55 U-654 rl PrOcMCR 0 4 2

R-CH

2

CH

2 COOH, COOH, or CH 2 COOH; Protected R wherein R=CH 2

CH

2 COOMe, COOMe, or CH 2 COOMo a) CH 2

N

2 ether b) H2,5%Pd/C c) uiphosgene. Et3N d) PhNH2,DMF e) LiOH,

THF/H

2 0 f) HCI/H 2 0 Pharmaceutically acceptable salts of compounds of Formula may be obtained in known manner, for example by treatment thereof with an appropriate amount of acid or base in the presence of a suitable solvent.

Another aspect of the present invention is the analogous process for producing a compound of Formula which process comprises reacting a compound of the formula

R

(R)m N (A) wherein R, RI and m are as defined for Formula with a compound of the formula: -N(X)(CR 13 R 1i4)vR20; wherein X, Ri 3

R

14 v and R 2 0 are as defined in Formula to yield a compound of Formula Alternatively, a compound of Formula (Al) 19- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:33 FROM-DCC .61392542770 T-632 P26/55 U-654 T N NH,

(R

1 )m wherein E, R, RI and m are as defined for Formula or a compound of Formula (A2)

R

I r-NH 2 wherein E, R, R 1 and m are as defined for Formula or may instead be reacted with a compound of the formula:

-N(X)-(CRI

3 Ri 4 )v wherein X, R 13

R

1 4, v and R 2 0 are as defined in Formula to yield a compound of Formula Another aspect of the present invention is the alternative process for producing a compound of Formula which process comprises reacting a compound of the formula:

R

(R,)rnm N0 (B) wherein RI, m and R are as defined for formula with a compound of the formula: NH2-(CRI3RI 4 )v wherein R13, R14, v and R20 are as defined in Formula to yield a compound of Formula and deprotecing the R group if necessary.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:33 FROM-DCC *61392542770 T-632 P27/55 U-654 As above, one may alternatively use a compound of Formula (B 1)

(R

1 )m wherein E, R, RI and m are as defined for Formula or a compound of Formula (B2) R N-0 wherein E, R, R and m are as defined for Formula or may instead be reacted with a compound of the formula: NH2-(CR3RI4)v R 20 wherein R 1 3 R 14, v and R 20 are as defined in Formula to yield a compound of Formula and deprotecting the R group if necessary.

In the Examples, all temperatures are in degrees Centigrade Mass spectra were performed upon a VG Zab mass spectrometer using fast atom bombardment, unless otherwise indicated. 1 H-NMR (hereinafter "NMR") spectra were recorded at 250 MHz or 400MHz using a Bruker AM 250 or Am 400 spectrometer, respectively. Multiplicities indicated are: s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet and br indicates a broad signal. Sat. indicates a saturated solution, equiv. indicates the proportion of a molar equivalent of reagent relative to the principal reactant.

Flash chromatography is run over Merck Silica gel 60 (230 400 mesh).

SYNTHETIC EXAMPLES The invention will now be described by reference to the foUowing examples which are merely illustrative and are not to be construed as a limitation of the scope -21.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:34 FROM-DCC +61392542770 T-632 P28/55 U-654 of the present invention. All temperatures are given in degrees centigrade, all solvents used herein are of the highest available purity and all reactions are run under anhydrous conditions in an argon atmosphere unless otherwise indicated.

Example 1 Preoaration of N-(3-Carboxyphenvl)-N'-(2-bromoohelyv)urea A solution of 3-amino benzoic acid (1 equivalent (hereinafter 1.37 gram (hereinafter in DMF was treated with 2-bromo phenyl isocyanate (1 eq.

1.98 g) at about 80C for about 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 1.28g of the titled compound as white solid. MS(ES)M-H=333Example 2 Preoaration of N-(3-Carboxvmethvlhpenvl)-N(2-bromohenyl)urea A solution of 3-amino phenyl acetic acid (leq, .151 g) in DMF was treated with 2-bromo phenyl isocyanate (1 eq, .198 g) at about 80 OC for about 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 0.32g of the titled compound as white solid.

MS(ES)M-H=347Examle 3 Pr paration of N-(3-Carboxvmethvlphenvl)-N'-(2.3-dichlorophenvllurea A solution of 3-amino phenyl acetic acid (leq, 151 milligrams (hereinafter in DMF was treated with 2,3-dichloro phenyl isocyanate (1 eq, 188 mg) at °C for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 12 g of the titled compound as white solid- MS(ES)M-H=337 Example 4 Preparation of N-(3-Carboxyphenvl)-N'-(2.3-dichlorophenvl)urea A solution of 3-amino benzoic acid (1 eq, 1.37 g) in DMF was treated with 2,3-dichloro phenyl isocyanate (1 eq, 1.88 g) at 80 oC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 1.01 g of the titled compound as white solid. MS(ES)M-H=323 Example 22.

COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:34 FROM-DCC +61392542770 T-632 P29/55 U-654 Preparation of N-3-(2-Carbovethyl)vheDvi1-N'-(2.3-dichloroPhepvl) urea a) 3-amino dihydrocinnamic acid A solution of 3-nitro dihydrocinnamic acid (500 mg) in ethyl acetate was treated with 10%Pd/C (500 mg). The resulting suspension was flushed with hydrogen and allowed to stir overnight at room temperature. The reaction mixture was purged with argon and then filtered through celite. The filtrate was concentrated and the residue was recrystallized from toluene and ethyl acetate. 1H NMR (DMSO) 6.95 t 6.4 m (3 2.7 t 2.45 t (2H) b) N-[3-(2-carboxyethyl)phenyl]-N'-(2,3-dicblorophenyl) urea A solution of 3-amino dihydro cinnamic acid (1 eq. 83 mg) in DMF was treated with 2,3-dichloro phenyl isocyanate (1 eq, 94 mg) at 80 oC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 0.037g of the titled compound as white solid. 1

H

NMR (DMSO) 9.45 s 8.47 s 8.17 d 7.31 m 7.24 t 6.88 d 2.73 t 2H), 2.54 t (2H) ExamplS 6 Preparation of N-(2.4-Dichloro-3-carboxy)-N-(2-bromophenyl) urea a) 5-amino 2,6-dichloro beozoic acid A solution of 5-nitro-2, 6-dichloro benzoic acid (2.0 g) in ethyl acetate was treated with 10% Pd/C(1.5g). The suspension was flushed with hydrogen and allowed to stir at room temperature overnight. The reaction mixture was purged with argon and filtered through celite. The filtrate was concentrated and the residue was purified by recrystalization from ethyl acetate and hexanes to afford the title compound (0.7g) as a white solid. IH NMR (DMSO) 7.15 d 6.8.d 5.74 s (IH, br) b) N-(2,4-Dichloro-3-carboxy)-N'-(2-bromophenyl) urea 23- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:34 FROM-DCC +61392542770 T-632 P30/55 U-654 A solution of 5-amino-2.6-dichloro benzoic acid (1 cq, 250 mng) in DMF was treated with 2-bromo phenyl isocyanate (1 eq, 153 uL-) at 80 oC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 35 mg of the titled compound as white solid.

MS(ES)M-H=401 Example 7 Preaaration of N-4-Chloro-3-carboxwhenvl-N'-(2-bromophcnvl)ura A solution of 5-amino-2-chloro benzoic acid (1 eq, 1.71 g) in DMF was treated with 2-bromo phenyl isocyanate (1 eq, 1.98 g) at 80 oC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 0.880 g of the titled compound as white solid. MS(ES)M-H=367 Examle 8 Preparation of N-(4-Chloro-3-carboxvhcnvl) N'-(2.3-dichlorohenyl urea A solution of S-amino-2-chloro beazoic acid (1 eq, 1.71 g) in DMF was treated with 2,3-dichloro phenyl isocyanate (1 eq, 1.88 g) at 80 oC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 1.57g of the utled compound as white solid- MS(ES)M- H=357EMmle 9 Preparation of N-(4-Chloro-3-carboxyphenvl)-N-(3-chlorophenyl)urea A solution of 5-amino-2-chloro benzoic acid (1 eq, 1.71 g) in DMF was treated with 3-chloro phenyl isocyanate (1 eq, 1.53 g) at 80 OC for 2 hours. The solution was cooled and the product was purified by recrystalization from methylene chloride and hexanes to afford 0.66g of the titled compound as white solid.

MS(ES)M-H=323 METHOD OF TREATMENT The compounds of Formula or a pharmaceutically acceptable salt thereof can be used in the manufacture of a medicament for the prophylactic or therapeutic treatment of any disease state in a human, or other mammal, which is exacerbated or caused by excessive or unregulated IL-8 cytokine production by such mammal's cell, -24- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:34 FROM-DCC +61392542770 T-632 P31/55 U-654 such as but not limited to monocytes and/or macrophages, or other chemokines which bind to the IL-8 a or |3 receptor, also referred to as the type I or type II receptor.

Accordingly, the present invention provides a method of treating a chemokine mediated disease, wherein the chbemokine is one which binds to an IL-S a or 0 receptor and which method comprises administering an effective amount of a compound of Formula or a pharmaceutically acceptable salt thereof. In particular, the chemokines are IL-8, GROoc, GROp, GROy, NAP-2 or ENA-78.

The compounds of Formula are administered in an amount sufficient to inhibit cytokine function, in particular IL-8, GROc. GROp, GROy, NAP-2 or ENA-78, such that they are biologically regulated down to normal levels of physiological function, or in some case to subnormal levels, so as to ameliorate the disease state.

Abnormal levels of IL-8, GROa, GROp, GROy, NAP-2 or ENA-78 for instance in the context of the present invention, constitute: levels of free IL-8 greater than or equal to I picogram per mL; (ii) any cell associated IL-8 GROG, GROO, GRy, NAP-2 or ENA-78 above normal physiological levels; or (iii) the presence IL-8, GROa, GRO0, GROy, NAP-2 or ENA-78 above basal levels in cells or tissues in IL-8, GROa, GROp, GROyNAP-2 or ENA-78 respectively, is produced.

The association of interleukin-8 and rhinovirus may be found in articles such as: Turner,et al., Clin. Infect. Dis. (1998), 26(4), 840-846; Sanders, et al., J. Virol.

(1998), 72(2). 934-942; Sethi, et al., Clin. Exp. Immunol. (1997), 110(3), 362-369; Zhu, et al., Am. J. Physiol. (1997), 273(4, Pt. L814-L824; Terajima, et al., Am. J.

Physiol. (1997), 273(4. Pt. L749-L759; Grunberg, et al., Clin- Exp. Allergy (1997), 27(1), 36-45; and Johnston, et al., J. Infect. Dis. (1997), 175(2), 323-329.

The association of interleukin-8 and osteoporosis may be found in articles such as: Streckfus et al., J. Gerontol., Ser. A (1997), 52A(6). M343-M351; Hermann, T. WO 95/31722; and Chaudhary, et al., Endocrinology (Baltimore) (1992), 130(5), 2528-34.

These diseases are primarily characterized by massive neutrophil infiltration, T-cell infiltration, or neovascular growth, and are associated with increased IL-8, COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:35 FROM-DCC +61392542770 T-632 P32/55 U-654 GROa, GRO. GROyor NAP-2 production which is responsible for the chermotaxis of neutrophils into the inflammatory site or the directional growth of endothelial cells. In contrast to other inflammatory cytokines (IL-1, TNF, and IL-6), IL-8.

GROo, GROJ, GROy or NAP-2 has the unique property of promoting neutrophil chcmotaxis, enzyme release including but not limited to elastase release as well as superoxide production and activation. The a-chemokines but particularly, GROo., GRO3, GROy or NAP-2, working through the IL-8 type I or II receptor can promote the neovaseularization of tumors by promoting the directional growth of endothelial cells. Therefore, the inhibition of IL-8 induced chemotaxis or activation would lead to a direct reduction in the neutrophil infiltration.

Recent evidence also implicates the role of chemokines in the treatment of HIV infections, Littleman et al., Nature 381, pp 661 (1996) and Koup et al., Nature 381, pp 667 (1996).

The present invention also provides for a means of treating, in an acute setting, as is well as preventing, in those individuals deemed susceptible to, CNS injuries by the chemokine receptor antagonist compounds of Formula CNS injuries as defined herein include both open or penetrating head trauma, such as by surgery, or a closed head trauma injury, such as by an injury to the head' region. Also included within this definition is ischemic stroke, particularly to the brain area.

Ischemic stroke may be defined as a focal neurologic disorder that results from insufficient blood supply to a particular brain area, usually as a consequence of an embolus, thrombi, or local atheromatous closure of the blood vessel. The role of inflanmmnatory cytokines in this are has been emerging and the present invention provides a mean for the potential treatment of these injuries. Relatively little treatment, for an acute injury such as these has been available.

Present evidence also indicates the use of IL-8 inhibitors in the treatment of atherosclerosis. The first reference, Boisvert et al., J Clia Invest, 1998, 101:353- 363 shows, through bone marrow transplantation, that the absence of IL-8 receptors on stem cells (and, therefore, on monocytes/macrophages) leads to a reduction in the -26- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:35 FROM-DCC +61392542770 T-632 P33/55 U-654 development of atherosclerotic plaques in LDL receptor deficient mice. Additional supporting references are: Apostolopoulos et al., Arterioscler Thromb Vase Biol.

1996, 16:1007-1012; Liu et al., Arterioscler Thromb Vasc Biol, 1997, 17:317-323; Rus et al., Atherosclerosis. 1996, 127:263-271.; Wang et al., J Biol Chem. 1996, 3 271:8837-8842; Yue et al., Eur J Pharmacol. 1993, 240:81-84; Koch et al., Am J Pathol, 1993, 142:1423-1431.; Lee et al., Immunol Lett, 1996, 53, 109-113.; and Terkeltaub et al., Arterioscler Thromb, 1994, 14:47-53.

TNF-a is a cytokine with proinflammatory actions, including endothelial leukocyte adhesion molecule expression. Leukocytes infiltrate into ischemic brain lesions and hence compounds which inhibit or decrease levels of TNF would be useful for treatment of ischeraic brain injury. See Liu et al., Stoke, Vol. 25., No. 7, pp 1481-88 (1994) whose disclosure is incorporated herein by reference.

Models of closed head injuries and treatment with mixed 5-LO/CO agents is discussed in Shohami et aL, J. of Vaise Clinical Physiology and Pharmacology, Vol. 3, No. 2, pp. 99-107 (1992) whose disclosure is incorporated herein by reference. Treatment which reduced edema formation was found to improve functional outcome in those animals treated.

The compounds of Formula are administered in an amount sufficient to inhibit IL-8, binding to the IL-8 alpha or beta receptors, from binding to these receptors, such as evidenced by a reduction in neutrophil chemotaxis and activation.

The discovery that the compounds of Formula are inhibitors of IL-8 binding is based upon the effects of the compounds of Formulas in the in vitro receptor binding assays which are described herein. The compounds of Formula have been shown, in some instances, to be dual inhibitors of both recombinant type'I and type I IL-8 receptors. Preferably the compounds are inhibitors of only one receptor, more preferably Type II.

As used herein, the term "IL-8 mediated disease or disease state" refers to any and all disease states in which IL-8, GROc, GROp. GROy, NAP-2 or ENA-78 plays a role, either by production of IL-8, GROc, GROp, GROy, NAP-2 or ENA-78 themselves, or by IL-8, GROc, GRO,. GROy, NAP-2 or ENA-78 causing another 27- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:35 FROM-DCC +61392542770 T-632 P34/55 U-654 monokine to be released, such as but not limited to IL-1, IL-6 or TNF. A disease state in which, for instance, IL-I is a major component, and whose production or action, is exacerbated or secreted in response to IL-8, would therefore be considered a disease stated mediated by IL-8.

As used herein, the term "chemokine mediated disease or disease state" refers to any and all disease states in which a chemokine which binds to an IL-8a or P receptor plays a role, such as but not limited IL-8, GROa, GROP, GROy, NAP-2 or ENA-78. This would include a disease state in which, IL-8 plays a role. either by production of IL-8 itself, or by IL-8 causing another monokine to be released, such as but not limited to IL-1, IL-6 or TNF. A disease state in which, for instance, IL- I is a major component, and whose production or action, is exacerbated or secreted in response to IL-8, would therefore be considered a disease stated mediated by IL-8.

Such diseases include but are not limited to psoriasis, atopic dermatitis, arthritis, asthma, chronic obstructive pulmonary disease, adult respiratory distress syndrome, inflammatory bowel disease, Crobn's disease, ulcerative colitis, stroke, septic shock, endotoxic shock, gram negative sepsis, toxic shock syndrome, cardiac and renal reperfusion injury, glomerulonephritis, thrombosis, graft vs. host reaction, alzheimers disease, allograft rejections, malaria, restinosis, angiogenesis, atherosclerosis, osteoporosis, gingivitis, undesired hematopoietic stem cells release and diseases caused by respiratory viruses, including but not limited to rhinovirus and influenza virus, herpesviruses, including but not limited to herpes simplex I and II, and hepatitis viruses, including but not limited to Hepatitis B and Hepatitis C virus.

As used herein, the term "cytokine" refers to any secreted polypeptide that affects the functions of cells and is a molecule which modulates interactions between cells in the immune, inflammatory or hematopoietic response. A cytokine includes, but is not limited to, monokines and lymphokines, regardless of which cells produce them. For instance, a monokine is generally referred to as being produced and secreted by a mononuclear cell, such as a macrophage and/or monocyte. Many other cells however also produce monokines, such as natural killer cells, fibroblasts, -28- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:36 FROM-DCC +61392542770 T-632 P35/55 U-654 basophils, neutrophils, endothelial cells, brain astrocytes, bone marrow stromal cells, epidermal keratinocytes and B-lympbocytes. Lymphokinecs are generally referred to as being produced by lymphocyte cells. Examples of cytokines include, but are not limited to, Interleukin-1 Interleukin-6 Interleukin-8 Tumor Necrosis Factor-alpha (TNF-j) and Tumor Necrosis Factor beta (TNF-B).

As used herein, the term "chemokine" refers to any secreted polypeptide that affects the functions of cells and is a molecule which modulates interactions between cells in the immune, inflammatory or hematopoietic response, similar to the term "cytokine" above. A chemokine is primarily secreted through cell transmembranes and causes chemotaxis and activation of specific white blood cells and leukocytes, neutrophils, monocytes, macrophages, T-cells, B-cells, endothelial cells and smooth muscle cells. Examples of chemokines include, but are not limited to, IL-8, GROo.

GROP, GROy, NAP-2, ENA-78, IP-10, MIP-la, MIP-P3 PF4, and MCP 1, 2, and 3.

In order to use a compound of Formula or a pharmaceutically acceptable salt thereof in therapy, it will normally be formulated into a pharmaceutical composition in accordance with standard pharmaceutical practice. This invention, therefore, also relates to a pharmaceutical composition comprising an effective, nontoxic amount of a compound of Formula and a pharmaceutically acceptable carrier or diluent.

Compounds of Formula pharmaceutically acceptable salts thereof and pharmaceutical compositions incorporating such may conveniently be administered by any of the routes conventionally used for drug administration, for instance, orally, topically, parenterally or by inhalation. The compounds of Formula may be administered in conventional dosage forms prepared by combining a compound of Formula with standard pharmaceutical carriers according to conventional procedures. The compounds of Formula may also be administered in conventional dosages in combination with a known, second therapeutically active compound. These procedures may involve mixing, granulating and compressing or dissolving the ingredients as appropriate to the desired preparation. It will be appreciated that the form and character of the pharmaceutically acceptable character 29- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:36 FROM-DCC +61392542770 T-632 P36/55 U-654 or diluent is dictated by the amount of active ingredient with which it is to be combined, the route of administration and other well-known variables. The carrier(s) must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.

The pharmaceutical carrier employed may be, for example, either a solid or liquid. Exemplary of solid carriers are lactose, terra alba, sucrose, tale, gelatin, agar, pectin. acacia, magnesium stearate, stearic acid and the like. Exemplary of liquid carriers are syrup, peanut oil, olive oil, water and the like. Similarly, the carrier or diluent may include time delay material well known to the art, such as glyceryl mono-stearate or glyceryl distearate alone or with a wax.

A wide variety of pharmaceutical forms can be employed. Thus, if a solid carrier is used, the preparation can be tableted, placed in a hard gelatin capsule in powder or pellet form or in the form of a troche or lozenge. The amount of solid carrier will vary widely but preferably will be from about 25mg. to about 1g. When is a liquid carrier is used, the preparation will be in the form of a syrup, emulsion, soft gelatin capsule, sterile injectable liquid such as an ampule or nonaqueous liquid suspension.

Compounds of Formula may be administered topically, that is by nonsystemic administration. This includes the application of a compound of Formula (I) externally to the epidermis or the buccal cavity and the instillation of such a compound into the ear, eye and nose, such that the compound does not significantly enter the blood stream. In contrast, systemic administration refers to oral, intravenous, intraperitoneal and intramuscular administration.

Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin to the site of inflammation such as liniments, lotions, creams, ointments or pastes, and drops suitable for administration to the eye, car or nose. The active ingredient may comprise, for topical administration, from 0.001% to 10% wlw, for instance from 1% to 2% by weight of the Formulation. It may however comprise as much as 10% w/w but COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:36 FHOII-DGC -61392542770 T-632 P37/55 U-654 preferably will comprise less than 5% w/w, more preferably from 0.1 to I% w/w of the Formulation.

Lotions according to the present in vention include those suitable for application to the skin or eye, An eye lotion may comprise a sterile aqueous solution optionally containing a bactericide and may be prepared by methods similar to those for the preparation of drops. Lotions or liniments for application to the skin may also include an agent to hasten drying and to cool the skin, such as an alcohol or acetone, and/or a moisturizer such as glycerol or an oil such as castor oil or arachis Oil.

Creams, ointments or pastes according to the present invention are semni-solid formulations of the active ingredient for external application. They -may be made by mixing the active ingredient in finely-.divided or powdered form, alone or in solution or suspension in an aqueous or nogn-aqueous fluid, with the aid of suitable machinery, with a greasy or non-greasy base. The base may comprise hydrocarbons such as hard, soft or liquid paraffin, glycerol, beeswax, a metallic soap; a mucilage; an oil of natural origin such as almond, corn, arachis, castor Or olive oil; wool fat or its derivatives or a fatty acid such as steric or olcic acid together with an alcohol such as propylene glycol or a maarogel. The formulation may incorporate any suitable surface active agent such as an anionic, cationic or non-ionic surfactant such as a sorbitan ester or a polyoxyetbylene derivative thereof. Suspending agents such as natural gums, cellulose derivatives or inorganic materials such as siicaceous silicas, and other ingredients such as lanolin, may also be included.

Drops according to the present invention may comprise sterile aqueous or oily solutions or suspensions and may be prepared by dissolving the active ingredient in a suitable aqueous solution of a bactericidal and/or fungicidal agent and/or any other suitable preservative, and preferably including a surface active agent. The resulting solution may then be clarified by filtration, trasferred to a suitable container which is then sealed and sterilized by autoclaving or maintaining at 98-100 0 C. for hlll an hour, Alternatively, the solution may be sterilized by filtration and transferred to the container by an aseptic technique. Examples of -31- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:37 FROM-DCC +61392542770 T-632 P38/55 U-654 bactericidal and fungicidal agents suitable for inclusion in the drops are phenylmercuric nitrate or acetate benzalkonium chloride and chlorhexidine acetate Suitable solvents for the preparation of an oily solution include glycerol, diluted alcohol and propylene glycol.

Compounds of formula may be administered parenterally. that is by intravenous, intramuscular, subcutaneous intranasal, intrarectal, intravagina] or intraperitoneal administration. The subcutaneous and intramuscular forms of parcnteral administration are generally preferred. Appropriate dosage forms for such administration may be prepared by conventional techniques. Compounds of Formula may also be administered by inhalation, that is by intranasal and oral inhalation administration. Appropriate dosage forms for such administration, such as an aerosol formulation or a metered dose inhaler, may be prepared by conventional techniques.

For all methods of use disclosed herein for the compounds of Formula the daily oral dosage regimen will preferably be from about 0.01 to about 80 mg/kg of total body weight. The daily parenteral dosage regimen about 0.001 to about mg/kg of total body weight- The daily topical dosage regimen will preferably be from 0.1 mg to 150 rmg, administered one to four, preferably two or three times daily. The daily inhalation dosage regimen will preferably be from about 0.01 mg/kg to about 1 mg/kg per day It will also be recognized by one of skill in the art that the optimal quantity and spacing of individual dosages of a compound of Formula or a pharmaceutically acceptable salt thereof will be determined by the nature and extent of the condition being treated, the form, route and site of administration, and the particular patient being treated, and that such optimums can be determined by conventional techniques. It will also be appreciated by one of skill in the art that the optimal course of treatment, the number of doses of a compound of Formula or a pharmaceutically acceptable salt thereof given per day for a defined number of days. can be ascertained by those skilled in the art using conventional course of treatment determination tests.

-32- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:37 FROM-DCC +61392542770 T-632 P39/55 U-654 The invention will now be described by reference to the following biological examples which are merely illustrative and are not to be construed as a limitation of the scope of the present invention.

BIOLOGICAL EXAMPLES The IL-8, and GRO-a chemokine inhibitory effects of compounds of the present invention were determined by the following in vitro assay: Receptor Binding Assays: [1251] IL-8 (human recombinant) was obtained from Amersham Corp., Arlington Heights, IL, with specific activity 2000 Ci/mmol. GRO-ca was obtained from NEN- New England Nuclear. All other chemicals were of analytical grade.

High levels of recombinant human IL-8 type ca and (3 receptors were individually expressed in Chinese hamster ovary cells as described previously (Holmes, et al., Science, 1991, 253, 1278). The Chinese hamster ovary membranes were homogenized according to a previously described protocol (Haour, et al., J Biol Chem., 249 pp 2195-2205 (1974)). Except that the homogenization buffer was changed to 10mM Tris-HCL, ImM MgS04, 0.5mM EDTA (ethylene-diaminetetraacetic acid), ImMPMSF (a-toluenesulphonyl fluoride), 0.5 mg/L Leupeptin, pH Membrane protein concentration was determined using Pierce Co. micro-assay kit using bovine serum albumin as a standard. All assays were performed in a 96-well micro plate format. Each reaction mixture contained 1251 IL-8 (0.25 nM) or 1251 Gro-ca and 0.5 pg/mL of IL-8Ra or 1.0 pg/mL of IL-8Ra membranes in 20 mM Bis- Trispropane and 0.4 mM Tris HCI buffers, pH 8.0, containing 1.2 rumM MgSO4, 0.1 mM EDTA, 25 mM NaCl and 0.03% CHAPS. In addition, drug or compound of interest was added which had been pre-dissolved in DMSO so as to reach a final concentration of between O.01uM and 100 uM. The assay was initiated by addition of 12 5 I-IL-8. After 1 hour at room temperature the plate was harvested using a Tomtec 96-well harvester onto a glass fiber filtermat blocked with 1% BSA and washed 3 times with 25 mM NaCl, 10 mM TrisHCl, 1 mM MgS04, 0.5 mM EDTA. 0.03 CHAPS, pH 7.4. The filter was -33- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:37 FROM-DCC *61392542770 T-632 P40/55 U-654 then dried and counted on the Betaplate liquid scintillation counter. The recombinant IL-8 Ra or Type I, receptor is also referred to herein as the nonpermissive receptor and the recombinant IL-8 Ra or Type II. receptor is referred to as the permissive receptor.

All of the exemplified compounds of Formulas noted herein in the Synthetic Chemistry Section, Example I to 9, demonstrated inhibitory in the permissive models for IL-8 receptor inhibition. The following compounds were found to be inactive in this assay: N-(2,4-Dichloro-3-carboxy)-N'-(2,3dichlorophenyl)urea; N-(3-Carboxyphenyl)-N'-(phenyl)urea and N-(3-Methylcarboxyphenyl)-N- (phenyl)urea.

Chemotaxis Assay; The in vitro inhibitory properties of these compounds are determined in the neutrophil chemotaxis assay as described in Current Protocols in Immunology, vol.

I, Supil 1, Unit 6.12.3., whose disclosure is incorporated herein by reference in its entirety. Neutrophils where isolated from human blood as described in Current Protocols in Immunology Vol. 1, Suppl 1 Unit 7.23.1, whose disclosure is incorporated herein by reference in its entirety. The chemoattractants IL-8, GROa, GROi, GROy and NAP-2 are placed in the bottom chamber of a 48 multiwell chamber (Neuro Probe, Cabin John, MD) at a concentration between 0.1 and 100 nM. The two chambers are separated by a 5um polycarbonate filter. When compounds of this invention are tested, they are mixed with the cells (0.001 1000 nM) just prior to the addition of the cells to the upper chamber. Incubation is allowed to proceed for between about 45 and 90 min. at about 37oC in a humidified incubator with 5% CO 2 At the end of the incubation period, the polycarbonate membrane is removed and the top side washed, the membrane then stained using the Diff Quick staining protocol (Baxter Products, McGaw Park. IL, USA). Cells which have chemotaxed to the cbemokine are visually counted using a microscope.

Generally, four fields are counted for each sample, these numbers are averaged to give the average number of cells which had migrated. Each sample is tested in -34- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:38 FROM-DCC +61392542770 T-632 P41/55 0-654 triplicate and each compound repeated at least four times. To certain cells (positive control cells) no compound is added, these cells represent the maximum chemotactic response of the cells. In the case where a negative control (unstimulated) is desired, no chemokine is added to the bottom chamber. The difference between the positive control and the negative control represents the chemotactic activity of the cells.

Elastase Release Assay: The compounds of this invention are tested for their ability to prevent Elastase release from human neutrophils. Neutrophils are isolated from human blood as described in Current Protocols in Immunology Vol. I, SuppI 1 Unit 7.23.1.

PMNs 0.88 x 106 cells suspended in Ringer's Solution (NaCl 118. KCI 4.56, NaHCO 3 25, KH 2

PO

4 1.03, Glucose 11.1, HEPES 5 mM, pH 7.4) are placed in each well of a 96 well plate in a volume of 50 ul. To this plate is added the test compound (0.001 1000 nM) in a volume of 50 ul, Cytochalasin B in a volume of ul (20ug/ml) and Ringers buffer in a volume of 50 ul. These cells are allowed to warm (37 5% C02, 95% RH) for 5 min. before IL-8, GROc, GROq3, GROy or NAP-2 at a final concentration of 0.01 1000 nM was added. The reaction is allowed to proceed for 45 min. before the 96 well plate is centrifuged (800 xg min.) and 100 ul of the supernatant removed. This supernatant is added to a second 96 well plate followed by an artificial elastase substrate (MeOSuc-Ala-Ala-Pro-Val- AMC, Nova Biochem, La Jolla, CA) to a final concentration of 6 ug/ml dissolved in phosphate buffered saline. Immediately, the plate is placed in a fluorescent 96 well plate reader (Cytofluor 2350. Millipore, Bedford, MA) and data collected at 3 min.

intervals according to the method of Nakajima et a] J. Biol. Chem. 254 4027 (1979).

The amount of Elastase released from the PMNs is calculated by measuring the rate of MeOSuc-Ala-Ala-Pro-Val-AMC degradation.

TNF-a in Traumatic Brain Injury Assay This assay provides for examination of the expression of tumor necrosis factor mRNA in specific brain regions, which follow experimentally, induced lateral fluidpercussion traumatic brain injury (TBI) in rats. Since TNF-c is able to induce nerve growth factor (NGF) and stimulate the release of other cytokines from activated COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:38 FROM-DCC -61392542770 T-632 P42/55 U-654 astrocytes, this post-traumatic alteration in gene expression of TNF-a plays an important role in both the acute and regenerative response to CNS trauma- A suitable assay may be found in WO 97/35856 or WO 97/49286 whose disclosures are incorporated herein by reference.

CNS Injury model for IL- mRNA This assay characterizes the regional expression of interleukin-lI (IL-1I) mRNA in specific brain regions following experimental lateral fluid-percussion traumatic brain injury (TBI) in rats. Results from these assays indicate that following TBI, the temporal expression of IL- 3 mRNA is regionally stimulated in specific brain regions. These regional changes in cycokines, such as IL-1B play a role in the posttraumatic pathologic or regenerative sequelae of brain injury. A suitable assay may be found in WO 97/35856 or WO 97/49286 whose disclosures are incorporated herein by reference.

In vivo Athereoschlerosis assay: In vivo models for measuring atherosclerosis in mice is based on the assay of Paigen et al with small modifications as described below. See Paigen B, Morrow A, Holmes PA, Mitchell D, Williams RA. Quantitative assessment of atherosclerotic lesions in mice. Atherosclerosis 68; 231-240 (1987); and Groot PHE, van Vlijmen BJM, Benson GM, Hofker MH, Schiffelers R, Vidgeon-Hart M, Havekes LM.

Quantitative assessment of aortic atherosclerosis in APOE*3 Leiden transgenic mice and its relationship to serum cholesterol exposure. Arterioscler Throrob Vase Biol.

16: 926-933 (1996).

Sectioning and staining of the aortic sinus Cross-sections of the aortic root arc taken as has been described previously Briefly, the hearts arc bisected just below the level of the atria and the base of the heart plus aortic root arc taken for analysis. After equilibrating the tissue in OCT compound overnight the hearts are immersed in OCT compound on a ciyostat chuck (Bright Instrument Company Ltd., UK) with the aorta facing the chuck- The tissue is frozen by surrounding the chuck with dry ice. The hearts are then sectioned perpendicular to the axis of the aorta, starting within the heart and working in the direction of the aorta. Once 36- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:38 FROM-ICC *61392542770 T-632 P43/55 U-654 the aortic root has been identified by the appearance of the three valve leaflets, alternate sections are taken and mounted on gelatinised slides. Sections arm air dried for I hour and subsequently rinsed briefly in 60% isopropyl alcohol. The sections are stained with Oil Red 0, counterstained with Mayer's haematoxylin, cover slipped using glycerol gelatin and sealed with nail varnish.

Quantification of atherosclerosis in the aortic root Ten alternate sections of the aortic root are imaged using an Olympus BH-2 microscope equipped with an 4x objective and a video camera (Hitachi, HV-C 10). Twenty-four bit colour images are acquired and analyzed using a PC (Datacell Pentium P5-133, Datacell, Berks, UK-) fitted with a franegrabbing board (Snapper, Active Imaging Ltd, Berks, and running Optinas software (version 5.1, Optimas Corp., WA, The images are captured under identical lighting, microscope, camera and PC conditions.

Quantification of the atherosclerotic lesion areas is performed by drawing around the lesions by hand using the Optimas software. Colour thresholds are set that quantify the areas that are stained red within the lesions. Absolute values for the cross-sectional areas of the lesions and the areas stained red are obtained by calibrating the software using an image of the grid on a haemocytomtr slide.

All publications, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fufly set forth.

The above description fully discloses the invention including prefen-ed embodiments thereof. Modifications and improvements of the embodiments specifically disclosed herein are within the scope of the following claims. Without further elaboration, it is believed that one skilled in the are can, using the preceding description, utilize the present invention to its fullest extent. Therefore the Examples herein are to be construed as merely illustrative and not a limitation of the -37- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:38 FROM-DCC +61392542770 T-632 P44/55 U-654 scope of the present invention in any way. The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows.

38- I I I COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11

Claims (2)

11-02-'04 18:39 FROM-DCC 61392542770 T-632 P45/55 U1-654 THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS: 1. A method of treating a chemokine mediated disease state, selected from the group consisting of malaria, restinosis, anglogenesis, atherosclerosis, osteoporosis, gingivitis, undesired hematopoictic stem cells release and diseases caused by respiratory viruses, herpesviruses, and hepatitis viruses, wherein the chemokine binds to an IL-8 a or A receptor in a mammal, which comprises administwring to said mammal an effective amount of a compound of the formula: W-N N-(CRR,.)v -R z I) wherein X is oxygen or sulfur; R is (CR 8 R 8 )r C(0) 2 H, (CR 8 R 8 )r NH-C(O)Ra, (CR8Rg)r C(O)NR 6 (CR 5 Rg)r NHS(0)2Rb. (CR 8 RS)r S(0)2NHRc, (CR 8 Rg)r NHC(X2)NHRb, or a tetrazolyl ring; X2 is oxygen or sulfur; RI is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted Cl- 10 alkyl; Cl- 1 o alkyl; C2-10 alkenyl; Ci-1o alkoxy; halosubstituted Cl- 0 alkoxy; (CRgRg)q S(O)tR4.: hydroxy: hydroxy Cl-4alkyl; aryl; aryl CI-4 alkyl; aryloxy; aryl Cl-4 alkyloxy; heteroaryl; heteroarylalkyl. heterocyclic, beterocyclic CI-4alkyl; heteroaryl C1-4 alkyloxy; aryl C2-10 alkenyl; beteroaryl C2-10 alkenyl; heterocyclic C2-10 alkenyl; (CRSRS)qNR 4 R 5 C2-1o alkenyl C(O)NR 4 R 5 (CRgR 8 )q C(O)NR 4 R 5 (CR 8 R 8 )q C(0)NR4R 1 o; S(0)3R 8 (CRgRg)q C(O)R 1 I C210 alkenyl C(O)Rj 1; C210 alkenyl QCO)ORI l(CR 8 Rg)q C(O)OR 12 (CR8R 8 )q OC(O) Rl (CRSR)qNR4C(o)Rll; (CRgRg)q NHS(0) 2 R 1 7 (CRgRg)q S(0)2NRAR; or two RI moieties together may form O-(CH 2 )sO- or a 5 to 6 membered saturated -39- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:39 FROM-DCC +61392542770 T-632 P46/55 U-654 or unsaturated ring; and wherein the aryl, heteroaryl, and heterocyclic containing moieties may be optionally substituted; n is an integer having a value of 1 to 3; m is an integer having a value of I to 3; i q is 0, or an integer having a value of I to r is 0, or an integer having a value of 1 to 4; s is an integer having a value of I to 3; t is 0, or an integer having a value of 1 or 2; v is an integer having a value of 1 to 4; R4 and R5 are independently hydrogen, optionally substituted CI-4 alkyl, optionally substituted aryl, optionally substituted aryl Cl-4alkyl, optionally substituted heteroaryl, optionally substituted heteroaryl Cl-4alkyl,. heterocyclic, or beterocyclic C 1.4 alkyl, or R4 and R5 together with the nitrogen to which they are attached form a 5 to 7 member ring which may optionally comprise an additional heteroatom selected from O/N/S; R6 and R7 are independently hydrogen or a CI-4 alkyl group, or R 6 and R7 together with the nitrogen to which they are attached form a 5 to 7 member ring which ring may optionally contain an additional heteroatom which heteroatom is selected from oxygen, nitrogen or sulfur; R6' and R7' are independently hydrogen, CI-4 alkyl, aryl, arylCi-4alkyl arylC2-4alkenyl, heteroaryl, heteroarylC-4alkyl, heteroarylC 2 4 alkenyl, heterocyclic, heterocyclic ClAalkyl, heterocyclic C2-4alkenyl moiety, provided that one of R6' and R7' are hydrogen, but not both; Y is independently selected from hydrogen; halogen; nitro; cyano; halosubstituted C- 1 10 alkyl; CI-10 alkyl; C2-IO alkenyl; CI-10 alkoxy; halosubstituted Cl. 10 alkoxy; azide; (CRsRg)q S(O)tR4; hydroxy; hydroxyCI-4alkyl; aryl; aryl C 1 4 alkyl; aryloxy: arylCl-4 alkyloxy; heteroaryl; heteroarylalkyl; heteroaryl C1-4 alkyloxy; heterocyclic, heterocyclic CI-4alkyl; aryl C2.1 0 alkenyl; heteroaryl C2-10 alkenyl; heterocyclic C 2 10 alkenyl; (CRgRg)q NR4R 5 C2-10 alkenyl COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:39 FROM-DCC +61392542770 T-632 P47/55 U-654 (CRgRs)q C(O)NR4R5; (CR8Rg)q C(O)NR4R10; S(0)3H; S(0)3R8; (CRgRg)q C(O)RI 1; C2-10 alkenyl C(O)R 1 i; C2-10 alkenyl C(O)OR 1; C(O)R 11; (CR 8 Rg)q C(O)ORI 2 (CRgR 8 )q OC(O) R 1 1 1 1 (CRgR8)q NHS(0) 2 Rd: (CR8Rg)q S(0)2NR 4 R 5 or two Y moieties together may form O-(CH2)sO- or a 5 to 6 membered saturated or unsaturated ring; and wherein the aryl, heteroaryl, and beterocyclic containing moieties may be optionally substituted; RS is independently selected from hydrogen or C1-4 alkyl; RIO is CI-10 alkyl C(0)2R8: RI is hydrogen, CI-4 alkyl. optionally substituted aryl, optionally.substituted aryl CI-4alkyl, optionally substituted heteroaryl, optionally substituted hcteroarylC1-4alkyl, optionally substituted heterocyclic, or optionally substituted heterocyclicC lI4alkyl; R12 is hydrogen, CI-10 alkyl, optionally substituted aryl or optionally substituted arylalkyl; R 1 3 and R14 are independently hydrogen, optionally substituted C 1- 4 alkyl, or one of R13 and RJ4 may be optionally substituted aryl; R 7 is CI-4alkyl, aryl, arylalkyl, heteroaryl, beteroarylCI 4alkyl, heterocyclic, or heterocyclicC1.4alkyl, wherein the aryl, beteroaryl and heterocyclic rings may all be optionally substituted; Ra is an alkyl, aryl, aryl Cl-4alkyl, heteroaryl, heteroaryl Cl-4alkyl, heterocyclic, or a heterocyclie C -4alkyl moiety, wherein all of thesc moieties may be optionally substituted; Rb is a NR6R7, alkyl, aryl. arylCl-4alkyl, arylC2-4alkenyl, heteroaryl, heteroarylC -4alkyl, beteroarylC2-4 alkenyl, heterocyclic, heterocyclic Ci-4alkyl, heterocyclic C24alkenyl moiety, or camphor, wherein all of these moieties may be optionally substituted; -41- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:39 FROM-DCC +61392542770 T-632 P48/55 U-654 Rc is alkyl. aryl, arylCi4alkyl. arylC2-4alkcuyl, heteroaryl, heteroarylC.-4alkyl, hetcroarylC2-4alkenyl, hetcrocyclic, heterocyclic C -4alkyl, or a hoterocyclic C2-4alkenyl moiety, all of which may be optionally substituted one to three times independently by halogen, nitro, halosubstituted C -4 alkyl, C -4 alkyl. CI-4 aikoxy, NRgC(O)Ra, C(O)NR6R7. S(0)3H, or C(O)OCI-4 alkyl; Rd is NR 6 alky), arylCi.4 alkyl, arylC 2-4 alkenyl, heteroaryl, heteroaryl-C l-4alkyl, heteroarylC 2 4 alkenyl, heterocyclic, or heterocyclicC 1-4 alkyl, wherein the aryl, hetcroaryl and heterocyclic containing moieties may all be optionally substituted; R R Y ((R 1 )m W is or E the E containing ring is optionally selected from O (R 1 )m 0 Ri or R1 the asterix denoting point of attachment of the ring; R 20 is WI, optionally substituted heteroaryl,. optionally substituted C 5 cycloalkyl, optionally substituted CI- 10 alkyl, optionally substituted C2- 10 alkenyl, or an optionally substituted C2- 10 alkynyl; n W is 7or -42- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:40 FROM-DCC +61392542770 T-632 P49/55 0-654 the E containing ring is optionally selected from S;n(Y) or n(Y) the asterix denoting point of attachment of the ring; or a pharmaceutically acceptable salt thereof. 2. The method according to Claim I wherein the R is (CRgRg)rC(0) 2 H. 3. The method according to Claim I wherein RI is halogen, cyano, nitro, CF3, alkenyl C(O)NR4RS, C(O) R4RIO, alkenyl C(O)OR12, heteroaryl, i0 beteroarylalkyl, heteroaryl alkenyl, or 4. The method according to Claim I wherein R 2 0 is W 1 The method according to Claim 1 wherein R 20 is heteroaryl. 6. The method according to Claim 4 wherein Y is halogen, C1-4 alkoxy, optionally substituted aryl, optionally substituted arylalkoxy, methylene dioxy, thioC -4alkyl, thioaryl. halosubstituted alkoxy, optionally substituted C1-4alkyl, hydroxy alkyl. 7- The method according to Claim 1 wherein RI is mono substituted in the 2- or 4- position, or di-substituted in the 2,4- position by an electron withdrawing moiety. -43- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'084 18:42 FHOM-DCC +61392542770 T-632 P50/55 U-654 P:e0ftgbDadnto U4.doee-A'O 8. Use of an effective amount of a compound of the formula: W-N A N-(R 13 nT)vF -R wherein X is oxygen or sulfur; R is (CRgR 8 )r C(O)) 2

14. (CRgRg)r NW C(O)Ra, (CRR& C(O)NR6,R7., NHS(Ofl2Rb. (CR 8 R 8 )r (CRgRg)r NHC(XZ)NHRb. or a tWtatolyl ring: X2 is OxYgen or sulfur, RjI is independently selected from hydrogen; halogen:, nitro; Cyano; halostbsuituted CI-j 0 alkyl; Cj.-1 0 alkyl; C 2 10 alkenyl; Cl. 10 alkocy; halosubstiruted Cj 1 alkoxy; (CR8Rg)q S(Q)tR 4 hydroxy; hydroxy Cl-4alkyl; axyl; aryl C 1 4 alkyl; aryloxy; aryl CI-4 aLkyloxy;* hereroaryl; heteroarylalkyl' heterocyclic, heterocyclic C:Aalkyl; fleteroaryl C].4 alkyloxy; aryl C2-1jQ alkeryl; heteroaryl C2- 10 alkenyl; heterocyclic C2-1lo alkenyl; (CRgRg)qNR4I 5 C2-1j 0 alkenyl C(O)NP 4 R 5 (CR 8 Rg)q C(O)Np4Rk 5 (CR 8 Rg)q C(O)NR4Rjo) S(O) 3 R 8 (CRgRg)q C(O)Ri i: C2-1o alkenyl C(O)Rj 1; C2-1lo alkenyl C(Q)0R II(CRg Rg)q C(O)OR 12; (CRgRg)q OC(O) RkII;; (CRsRs)qNR4~c(o)R 11; (CR 8 Rg)q NHiS(O) 2 R 2 1 7 (CRgRg)q S(O)2.NR 4 R 5 or two R I moieties together may form O-(Cl1 2 )sO- or a 5 to 6 mernbered saturated 44 COMS ID No: SMBI400613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02--'04 18:40 FHOM-DCC +632470T62P15 +61392542770 T-632 P51/55 U-654 Or unsaturated ring; and wherein the amyl, hecteroaryi, and hecerocyciic containing moieties may be optionally substituted; n. is an integer having a value of I to 3;, m is ant integer having a value of I to 3; q is 0, or an integer having a value of I to r is 0, or an integer having a value of I to 4; s is an integer having a value of 1 to 3; t is 0, or an integer having a value of 1 or 2; v is an integer having a value of 1 to 4; R4 and R5 are independently hydrogen, optiaonally substituaed C 1 -4 alkyl. Optionally substituted aryl, optionally substituted aryl C1..4alky1, option ally substituted he teroaryl, optionally substituted heteroaryl Cj 4ulkyI, hetrerocyclic, or heterocyclic C 1 -4 alkyl, or R4 and R5 together with the nitrogen~ to which they arc, attached form a 5 to 7 member ring which may optionally compiise an additional heteroacorn selected from 0/Ni'S; R6 and R7 are independently hydrogen or a Cj- 4 aikyl group, or R6 and R 7 together with the nitrogen to which they are attached form a 5 to 7 member ring which ring may optionally contain an additional heteroatom which beteroatom is Selected from oxygen, nitrogen or sulfur; and R7'are independently hydrogen, Ci1 4 alkyl, awyl, arvlCpI 4alky], arYlC2-4alkenyI, hetcroaxyi, heteroar}4c j .4allkyl, heteroaryIC 2 4 alkenyi, heterocyclic, heterocyclic CJI..4aflcyl, heterocyclic CZ..4alkenyl moiety, provided that one of R6, and R,7'are hydrogen, but not both;, Y is independently selected frm hydrogen; halogen; nitro-, cyano; halosubstiute~d C 1 1 0 alkyl; Cp 1 0 alkyl; C2- 10 ailcenyl; CP-lo alicoxy; halosubstimted C1 1 0 alicoxy; azide; (CRgRg)g S(O)tR 4 hydroxy; hydroxyCl- 4 alkj.ayl; ar yl C]I._4 alkyl; aryloxy; aiylCj- 4 alkyloxy; hetcroaryi; heteroaiylaiiyj. beteroaryj C 1 4 aLkyloxy; het erocyciic, heterocycic CjI -4alkyl; aryl C2-1j 0 alkenyi; heteroaiyj C 2 1 0 alkenyJ; heterocyclic C2- lo alienyl; (CRgRg)q NPR&; C 2 10 aikenyl COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:40 FROM-DCC +61392542770 T-632 P52/55 U-654 C(O)NR 4 R 5 (CRsR8)q C(O)NR 4 Rs; (CRgRg)q C(0)NR4 1 0 S(0)3H; S(0)3R8; (CRsR8)q C(0)Rj 1; C2-10 alkenyl C(O)R 1 I; C2-10 alkenyl C(O)ORI C(O)RI 1; (CR 8 Rg)q C(0)OR 12 (CR8R8)q OC(O) R11; (CR8R8)qNR 4 C(0)R 11 (CR8RS)q NHS(O) 2 Rd; (CR8gR)q S(O)2NR4R5; or two Y moieties together may form O-(CH2)sO- or a 5 to 6 membered saturated or unsaturated ring; and wherein the aryl. heteroaryl, and heterocyclic containing moieties may be optionally substituted; R8 is independently selected from hydrogen or C1-4 alkyl; RlO.is CI-10 alkyl C(0)2R 8 Rj is hydrogen, C 1 4 alkyl, optionally substituted aryl, optionallysubstituted aryl Cl-4alkyl, optionally substituted heteroaryl, optionally substituted heteroarylC -i4alky, optionally substituted heterocyclic, or optionally substituted heterocyclicCl-4alkyl; R12 is hydrogen, C1- 0 alkyl. optionally substituted aryl or optionally substituted arylalky; R 13 and R 14 are independently hydrogen, optionally substituted C1- 4 alkyl, or one of R13 and RI4 may be optionally substituted aryl; R 17 is C1-4alkyl, aryl, arylalkyl, heteroaryl, beteroarylC1-4alkyl, heterocyclic, or heterocyclicCl-4alkyl, wherein the aryl, heteroaryi and heterocyclic rings may all be optionally substituted; Ra is an alkyl, aryl, aryl Cl-4alkyl, heteroaryl, heteroaryl Cl-4alkyl, heterocyclic, or a heterocyclic C1.4alkyl moiety, wherein all of these moieties may be optionally substituted; Rb is a NR6R 7 alkyl, aryl, arylCl4alkyl, arylC2-4alkenryl, heteroaryl, heteroarylC 4 alkyl, heteroarylC 2 4 alkenyl, heterocycie, beterocycijc C -4alkyl, heterocyclic C2-4alkenyl moiety, or camphor, wherein all of these moieties may be optionally substituted; 46 COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:41 FROM-DCC +61392542770 T-632 P53/55 U-654 Rc is alkyl, aryl, arylC-4alkyl, ary1C2-4alkenyl, heteroaryl, hcteroarylC 1 .4alkyl, heteroarylC2-4alkenyl, heterocyclic, heterocyclic C -4alkyl. or a heterocyclic C2-4alkenyl moiety, all of which may be optionally substituted one to three times independently by halogen, nitro. halosubstituted CI-4 alkyl, C1- 4 alkyl. C -4 alkoxy, NR9C(O)Ra, C(O)NR6R7, S(0)3H,. or C()OC 1-4 alkyl; Rd is NR 6 R7, alkyl, arylC 14 alkyl, arylC 2-4 alkenyl, beteroaryl, heteroaryl-C -4alkyl, heteroarylC 2 -4 alkenyl, heterocyclic, or heterocyclicC -4 alkyl, wherein the aryl, heteroaryl and heterocyclic containing moieties may all be optionally substituted; R R S (R (R,)r W is or the E containing ring is optionally selected from O or R the asterix denoting point of attachment of the ring; R 2 0 is WI, optionally substituted heteroaryl, optionally substituted C 5 8 cycloalkyl, optionally substituted C.O 1 0 alkyl. optionally substituted C 2 10 alkenyl, or an optionally substituted C2. 10 alkynyl; Y)n Y)n W l is EP or 47 COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11 11-02-'04 18:41 FROM-DCC +61392542770 T-632 P54/55 U-654 the E' containing ring is optionally selected from 0 ;or the asterix denoting point of attachment of the ring; or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for treating a chemokine mediated disease selected from the group consisting of malaria, restinosis, angiogenesis, atherosclerosis, osteoporosis, gingivitis, undesired hematopoictic stem cells release and diseases caused by respiratory viruses, herpesviruses, and hepatitis viruses, wherein the chemokine binds to an IL-8 a or P receptor in a mammal. 9. A method of treating a chemokine mediated disease state according to claim 1, substantially as hereinbefore described. Use of an effective amount of a compound according to claim 8, substantially as hereinbefore described. DATED this 11th day of February SmithKline Beecham Corporation By DAVIES COLLISON CAVE Patent Attorneys for the Applicants -48- COMS ID No: SMBI-00613490 Received by IP Australia: Time 18:27 Date 2004-02-11