NZ515621A - Medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits - Google Patents

Medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits

Info

Publication number
NZ515621A
NZ515621A NZ515621A NZ51562100A NZ515621A NZ 515621 A NZ515621 A NZ 515621A NZ 515621 A NZ515621 A NZ 515621A NZ 51562100 A NZ51562100 A NZ 51562100A NZ 515621 A NZ515621 A NZ 515621A
Authority
NZ
New Zealand
Prior art keywords
phenylamino
phenyl
benzoic acid
ethyl
dichloro
Prior art date
Application number
NZ515621A
Inventor
Corinne Elizab Augelli-Szafran
Mark Robert Barvian
Christopher Franklin Bigge
Shelly Ann Glase
Shunichiro Hachiya
John Steven Kiely
Takenori Kimura
Yingjie Lai
Annette Theresa Sakkab
Mark James Suto
Larycraswell Walker
Tomoyuki Yasunaga
Nian Zhuang
Original Assignee
Warner Lambert Co
Yamanouchi Pharma Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Warner Lambert Co, Yamanouchi Pharma Co Ltd filed Critical Warner Lambert Co
Publication of NZ515621A publication Critical patent/NZ515621A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C07D213/82—Amides; Imides in position 3
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/402—1-aryl substituted, e.g. piretanide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/52—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C229/54—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C229/56—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring with amino and carboxyl groups bound in ortho-position
    • C07C229/58—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring with amino and carboxyl groups bound in ortho-position having the nitrogen atom of at least one of the amino groups further bound to a carbon atom of a six-membered aromatic ring, e.g. N-phenyl-anthranilic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/52—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C229/54—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C229/62—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring with amino groups and at least two carboxyl groups bound to carbon atoms of the same six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/52—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C229/54—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C229/64—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring the carbon skeleton being further substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/51—Y being a hydrogen or a carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/88—Nitrogen atoms, e.g. allantoin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/58—Radicals substituted by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)

Abstract

Described is the use of compounds of formula (I) in the manufacture of medicaments for the treatment of Alzheimer's disease and the inhibition of amyloid deposits, wherein A is CH or N; and the remaining substituents are defined herein.

Description

<div class="application article clearfix" id="description"> <p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number 515621 <br><br> 515621 <br><br> WO 00/76489 PCT/USO0/15071 <br><br> MEDICAMENTS FOR INHIBITING AMYLOID PROTEIN AGGREGATION AND METHODS OF IMAGING AMYLOID DEPOSITS <br><br> FIELD OF THE INVENTION <br><br> This invention relates to medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits. More particularly, this invention relates to medicaments for inhibiting amyloid protein aggregation in order to treat Alzheimer's disease. <br><br> BACKGROUND OF THE INVENTION <br><br> Amyloidosis is a condition characterized by the accumulation of various insoluble, fibrillar proteins in the tissues of a patient. The fibrillar proteins that comprise the accumulations or deposits are called amyloid proteins. While the particular proteins or peptides found in the deposits vary, the presence of fibrillar morphology and a large amount of (5-sheet secondary structure is common to many types of amyloids. An amyloid deposit is formed by the aggregation of amyloid proteins, followed by the further combination of aggregates and/or amyloid proteins. <br><br> The presence of amyloid deposits has been shown in various diseases, <br><br> each with its particular associated protein, such as Mediterranean fever, Muckle- . Wells syndrome, idiopathetic myeloma, amyloid polyneuropathy, amyloid cardiomyopathy, systemic senile amyloidosis, <br><br> hereditary cerebral hemorrhage with amyloidosis, Alzheimer's disease, Down's syndrome, Scrapie, Creutzfeldt-Jacob disease, Kuru, Gerstmann-Straussler-Scheinker syndrome, medullary carcinoma of the thyroid, Isolated atrial amyloid, fb-microglobulin amyloid in dialysis patients, inclusion body myositis, <br><br> fb-amyloid deposits in muscle wasting disease, Sickle Cell Anemia, Parkinson's <br><br> Disease, and Islets of Langerhans diabetes Type II insulinoma. ' 1 <br><br> WO 00/76489 <br><br> PCT/USOO/l 5071 <br><br> -2- <br><br> Alzheimer's disease is a degenerative brain disorder characterized clinically by progressive loss of memory, cognition, reasoning, judgement, and emotional stability that gradually leads to mental deterioration and ultimately death. Because Alzheimer's disease and related degenerative brain disorders are a major medical issue for an increasingly aging population, the need for new treatments and methods for diagnosing the disorders are needed. <br><br> A simple, noninvasive method for detecting and quantitating amyloid deposits in a patient has been eagerly sought. Presently, detection of amyloid deposits involves histological analysis of biopsy or autopsy materials. Both methods have major drawbacks. For example, an autopsy can only be used for a postmortem diagnosis. <br><br> The direct imaging of amyloid deposits in vivo is difficult, as the deposits have many of the same physical properties (i.e., density and water content) as normal tissues. Attempts to image amyloid deposits directly using magnetic resonance imaging (MR!) and computer-assisted tomography (CAT) have been disappointing and have detected amyloid deposits only under certain favorable conditions. In addition, efforts to label amyloid deposits with antibodies, serum amyloid P protein, or other probe molecules has provided some selectivity on the periphery of tissues, but has provided for poor imaging of tissue interiors. <br><br> Thus, it would be useful to have a noninvasive technique for imaging and quantitating amyloid deposits in a patient. In addition, it would be useful to have compounds that inhibit the aggregation of amyloid proteins to form amyloid deposits. <br><br> SUMMARY OF THE INVENTION <br><br> The present invention provides a use of a therapeutically effective amount of a compound of Formula I <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> o- <br><br> R <br><br> R <br><br> \ <br><br> (ch2)- <br><br> R" <br><br> wherein <br><br> 0 <br><br> 1 <br><br> Ra is hydrogen, Cj-Cg alkyl, or -CCj-Cg alkyl; <br><br> n is 1 to 5 inclusive; <br><br> Rl, R^, r3; r4? ^ p7 ^ independently hydrogen, halogen, <br><br> -OH, -NH2, NRbRc, -C02H, -C02C^Cg alkyl, -N02, -OCi-C12 alkyl, -Cj-Cg alkyl, -CF3, -CN, -OCH? phenyl, -OCH2-substituted phenyl,--(CH2)m-phenyl, -0-phenyI, -O-substituted phenyl, <br><br> 0 O <br><br> 1 I! <br><br> -CH=CH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C ! -C6alkyl)(CH2)pNRbRc, <br><br> /CH2OCj-C6 alkyl <br><br> —CH \ <br><br> CH2OCj-C6 alkyl <br><br> R^ is COOH, tetrazolyl, -S02R^, or -C0NHS02R^; <br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m-phenyl, or <br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-C]-Cg alkylpiperazinyl, morpholino, <br><br> thiomorpholino, decahydroisoquinoline, or pyrazolyl; <br><br> R^ is hydrogen, -Cj-Cg alkyl, -CF3, or phenyl; <br><br> m is 0 to 5 inclusive; | <br><br> p is 1 to 5 inclusive; | 11 ^ <br><br> A is CH or N; f f vsr <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -4- <br><br> Rl and R^, when adjacent to one another, can be methylene-dioxy; or pharmaceutically acceptable salts thereof, in the manufacture of a medicament for treating Alzheimer's disease. <br><br> In a preferred embodiment, the _/ group is attached at the 4-position of the phenyl ring. <br><br> In a preferred embodiment of the use, in the compounds of Formula I <br><br> Ra is hydrogen; <br><br> n is 2; and <br><br> R3 and R^ are hydrogen. <br><br> In a preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> Rl is halo; <br><br> R^ is hydrogen or halo; <br><br> r^, r4, r5; and r6 ^ hydrogen; and n is 2 to 5 inclusive. <br><br> In another preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> n is 2 or 3; <br><br> Rl is -NRbRC; and , w j.4 <br><br> r^, r3, r4s r5^ r7 are hydrogen. jj <br><br> In a preferred embodiment of the use, in the compounds of Formula I jj <br><br> Ra is hydrogen; ' = <br><br> n is 2; <br><br> R3 and R^ are hydrogen; and <br><br> Rl, R^, and R^ are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -CF3, phenyl, hydrogen, -OCH2 phenyl, <br><br> WO 00/76489 PCT/USOO/15071 <br><br> -5- <br><br> -0(CH2)bN(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, <br><br> N— <br><br> , -N[(CH2)3CH3]2, substituted phenyl, -OCH2-substituted phenyl, pyrrozolyl, or -N(phenyl)2. <br><br> 5 In a preferred embodiment of the use, in the compounds of Formula I <br><br> Ra is hydrogen; <br><br> n is 3, 4, or 5; <br><br> and R4 are hydrogen; and Rl, R^, and R^ are independently chlorine or hydrogen. <br><br> 10 In a preferred embodiment of the use, in the compounds of Formula I <br><br> Ra is hydrogen; <br><br> n is 2; <br><br> r3 and R4 are hydrogen; and <br><br> R5, r63 and R&amp; are independently hydrogen, -C02H, -N02, -OCH3, <br><br> 15 O <br><br> » <br><br> imidazolyl, -SCH3, -CN, fluorine, -CH3, -CF3, halogen, <br><br> I <br><br> O <br><br> 20 -NH-C1 -Cg alkyl, -N(C]-Cgalkyl)2, -NH2, or pyrrolyl. <br><br> In a preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> nis 2; r'Y'-K <br><br> R3 and R^ are hydrogen; and I , ., ■ <br><br> I 21 <br><br> 25 R^ is -CO?H. | <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> • R <br><br> Also preferred is a use of a therapeutically effective amount of a compound of Formula I <br><br> R3 R5 <br><br> &lt;CH2)^=P^ Ja wherein <br><br> 5 Ra is hydrogen; <br><br> n is 1 to 5 inclusive; <br><br> R^ and R^ are hydrogen; <br><br> R', R^, and R- are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -CF^pEenyl", hydrogen, -OCffvphenyl, TO- -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, <br><br> -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, -N[(CH2)3CH3]2, substituted phenyl, -OCH2-substituted phenyl, pyrazolyl, or -N(phenyl)2; <br><br> r5 and R^ are independently hydrogen, -C02H, -NO2, -OCH3, 15 imidazolyl, -CN, fluorine, -CH3, -CF3, or pyrrolyl; <br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a , medicament for treating Alzheimer's disease. <br><br> In a preferred embodiment of the use, compounds of Formula I are <br><br> 2-{4-[2-(3,4-Dichlorophenyl)ethyl]phenylamino}-benzoic acid; 20 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino } -5-nitrobenzoic acid; <br><br> 2- {4-[4-(3,4-Dichloro-phenyl)-ethyl]phenylamino }-4-methoxy-5-nitrobenzoic acid; <br><br> 2- {4-[2-(3,4-Dihydroxy-phenyl)-ethyl]-phenylamino} benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}benzoic acid; 25 2-{4-[2-(3,4,5-Trihydroxy-phenyI)-ethyl]phenylamino}benzoic acid; <br><br> cry <br><br> &lt; 5 <br><br> 6 U i!-L I] -{O Cxj <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -7- <br><br> 2- {4-[3 -(3,4-Dichlorophenyl)propyl]phenylamino } -4-methoxy-5-nitrobenzoic acid; <br><br> 2- {4-[3 -(3,4-Dichlorophenyl)propyl]phenylamino } -4-imidazo-1 -yl-5-nitrobenzoic acid; <br><br> 2- {4-[3 -(3,4-Dichlorophenyl)-propyI]phenylamino } benzoic acid; 2-{4-[4-(3,4-Dichlorophenyl)butyl]phenylamino}benzoic acid; 2- {4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamino} -5-nitro-benzoic acid; 2-{4-[4-(3,4-Dichlorophenyl)-butyl]phenylamino}-3,5-dinitrobenzoic acid; <br><br> 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino] -benzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyI]-phenylamino}-5-nitro-benzoic acid; 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenyiamino}-5-nitro-benzoic acid; 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid; 2-(4-Phenethyl-phenylamino)-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-terephthalic acid; 2-{4-[2-(3,4-DichIoro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic acid; <br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methanesulfonyl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyIamino}-5-imidazol-l-yl-benzoic acid; <br><br> 2-{4-[2-(3,4-DichIoro-phenyl)-ethyl]-phenyiamino}-6-nitro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-nitro-benzoic acid; 2-{4-[2-(3,4-DichIoro-phenyl)-ethyl]-phenyIamino}-3-nitro-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> acid; acid; <br><br> -8- <br><br> 5-Cyano-2-{4-[2-(3,4-dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-{3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4)6-difluoro-benzoic <br><br> 6-{4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -2,3 -difluoro-benzoic <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-methyl-benzoic acid; <br><br> 10 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-fluoro-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3,5-difluoro-benzoic acid; <br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -3 -trifluoromethyl-benzoic acid; <br><br> 15 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -6-trifluoromethyl- <br><br> benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]-phenylamino}-5-pyrrol-l-yl-benzoic <br><br> 20 acid; <br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4- {2-[4-(3-Dimethylamino-propoxy)-phenyl] -ethyl} -phenylamino)-benzoic acid; <br><br> 2-{4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; 25 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino} -benzoic acid; <br><br> 2-{4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[4-(2-Ethoxy-l-ethoxymethyl-ethyl)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 2- {4- [2-(4-Pyrrol-1 -yl-phenyl)-ethyl] -phenylamino } -benzoic acid; 30 2-{4-[2-(4-Styryl-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4'-Ethyl-biphenyl-4-yl)-ethyl]-phenylamino}-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -9- <br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyl]-phenylamino}-benzoicacid; <br><br> 2-(4- {2- [3 -(3,5-Dichloro-phenoxy)-phenyl] -ethyl} -phenylamino)-benzoic acid; <br><br> 2-(4- {2- [4-(2-Chloro-6-fluoro-benzyloxy)-phenyl]-ethyl} -phenylamino)-benzoic acid; <br><br> 2-{4-[2-(4-Pyrazol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoicacid; 2-(4-{2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-amino-benzoic acid; <br><br> 2- {4- [2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino } -5-trifluoromethyl-benzoic acid; <br><br> 2- {4- [2-(3,4-Dichlorophenyl)]phenylamino } -5 -nitrobenzoic acid; 2- {4-[2-[(3,4-Dichlorophenyl)propyl]phenylamino} -5-nitrobenzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyI)-ethyI] phenylamino}-5-nitrobenzoic acid; 2-[[4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenyI]amino-benzoic acid; <br><br> 2-{4-[3-(4-Diethylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Nitrophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Nitrophenyl)propyl]phenylamino}benzoic acid; 2- {4-[3-(4-Aminophenyl)propyl]phenylamino } benzoic acid; 2-{ 4-[3-(3-Aminophenyl)propyl]phenylamino } benzoic acid; 2-{4-[2-(4-Aminophenyl)ethyl]phenylamino}benzoic acid; 2- {4-[2-(4-Dipropylaminophenyl)ethyl]phenyIamino } benzoic acid monohydrochloride; <br><br> 2-{4-[2-(4-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride monohydrate; <br><br> 2-{4-[3-(3-Dipropylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Dimethylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Ethylaminophenyl)propyl]phenylamino}benzoic acid; 2-(N-{4-[3-(4-Diethylaminophenyl)propyl]phenyl}-N-ethylamino)benzoic acid; <br><br> WO 00/76489 <br><br> PCT/U S00/15071 <br><br> -10- <br><br> 2-{4-[2-(3-Dibenzylaminophenyl)ethyl]phenylamino}benzoic acid; 2-{4-[3-(3-Diethylaminophenyl)propyl]phenylamino}benzoic acid; 2- {4-[2-(3-Aminophenyl)ethyl]phenylamino} benzoic acid; 2-{4-[3-(4-Dimethylaminophenyl)propyl]phenylaimno}benzoic acid; 5 2-{4-[2-(4-Acetylaminophenyl)ethyl]phenylamino}benzoic acid; <br><br> 2-{4-[2-(3-Acetylaminophenyl)ethyl]phenylamino}benzoic acid; 2-{4-[2-(3-Dipropylaminophenyl)ethyl]phenylamino} benzoic acid monohydrochloride; <br><br> 2-{4-[2-(3-Dibutylaminophenyl)ethyl]phenylamino}benzoic acid 10 monohydrochloride; <br><br> 2-{4-[3-(4-Acetylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Acetylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride; <br><br> 15 2-{4-[2-(3-Piperidin-l-ylphenyl)ethyl]phenyiamino}benzoic acid monohydrochloride; <br><br> 2-{4-[3-(4-Dipropylaminophenyl)propyl]phenylamino}benzoic acid; 2- {4-[3 -(4-Dibutylaminophenyl)propyl]phenylamino } benzoic acid; 2-{4-[3-(3-Dibutylaminophenyl)propyl]phenylamino}benzoic acid; 20 2-(4-{3-[4-(lH-Pyrrol-l-yl)phenyl]propyl}phenylamino)benzoic acid; <br><br> 2-{4-[3-(4-Piperidin-l-ylphenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Diethylcarbamoylphenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Carboxyphenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Diethylaminomethylphenyl)propyl]phenylamino}benzoic acid; 25 2-{4-[3-(4-Propylaminophenyl)propyl]phenylamino}benzoic acid; <br><br> 2-{4-[3-(3-Propylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Pyrrolidin-l-yl-phenyl)-propyl]-phenylamino}-benzoic acid; 2-{4-[3-(3-Piperidin-lyl-phenyl)-propyl]-phenylamino}-benzoic acid; 2-{4-[3-(4-[2-Diethylaminoethylamino]phenyl)-propyl]phenylamino}-30 benzoic acid; <br><br> 2-{4-[2-(4-[Hydroxycarbonylmethylamino]phenyl)ethyl]phenylamino}-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/1507] <br><br> -11- <br><br> 2-{4-[2-(4-[2-Diethyiaininoethylamino]phenyl)ethyl]phenylamino}-benzoic acid; <br><br> 2- {4- [3 -(4-Morpholinophenyl)propyl]phenylamino } -benzoic acid; <br><br> 2- {4-[3 -(4-Piperazinylphenyl)propyI]phenylamino } -benzoic acid; and <br><br> 2-[4-(3,4-Dichlorophenyl)phenylamino]benzoic acid. <br><br> The invention also provides the foregoing compounds wherein the benzoic acid portion is replaced with a pyridyl carboxylic acid, for example, 4-[4-(3,4-dichiorophenyl)phenylamino]-3-hydroxycarbonylpyridine. <br><br> Also provided is a use of a compound of Formula I <br><br> Ra is hydrogen, Cj-Cg alkyl, or -CCj-Cg alkyl; <br><br> n is 0 to 5 inclusive; <br><br> Rl, R^, r3, r4? r5} r6? and r7 ^ independently hydrogen, halogen, <br><br> -OH, -NH2, NRbRc, -C02H, -C02C]-C6 alkyl, -N02, -OCi-C12 alkyl, -C]-Cg alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyl, -O-phenyl, -O-substituted phenyl, <br><br> 1 <br><br> wherein <br><br> O <br><br> O <br><br> o <br><br> I <br><br> -CH=CH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C ] -C6alkyl)(CH2)pNRbRc, <br><br> -12- <br><br> /CH^OCj-Cgalkyl <br><br> —CH <br><br> \ <br><br> CH2OCrC6 alkyl R8 is COOH, tetrazolyl, -S02Rd, or -C0NHS02Rd; <br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m-phenyl, or <br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-Cj-Cg alkylpiperazinyl, morpholino, <br><br> thiomorpholino, decahydroisoquinoline, or pyrazolyl; <br><br> Rd is hydrogen, -Cj-Cg alkyl, -CF3, or phenyl; <br><br> m is 0 to 5 inclusive; <br><br> p is 1 to 5 inclusive; <br><br> A is CH or N; <br><br> Rl and R2, when adjacent to one another, can be methylene-dioxy; <br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for inhibiting the aggregation of amyloid proteins to form amyloid deposits. <br><br> In a preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> n is 2; and <br><br> R^ and R^ are hydrogen. <br><br> In a preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> R^ and R^ are hydrogen; and n is 2 to 5 inclusive. <br><br> In a preferred embodiment of the use, <br><br> Ra is hydrogen; <br><br> n is 2; <br><br> R^ and R^ are hydrogen; and in the compounds of Formula I <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -13- <br><br> Rl, R^, and are independently chlorine, -N(CH?CH3)2, -OH, CH3-, fluorine, -CF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, <br><br> In a preferred embodiment of the use, in the compounds of Formula I <br><br> Ra is hydrogen; <br><br> n is 3,4, or 5; <br><br> R^ and R^ are hydrogen; and <br><br> In a preferred embodiment of the use, in the compoimds of Formula I Ra is hydrogen; <br><br> R^ and R^ are independently hydrogen, -CO2H, -N02, -OCH3, imidazolyl, -CN, fluorine, -CH3, -CF3, halogen, -NH-C]-Cg alkyl, -N(C}-Chalky] )2, -NH2, or pyrrolyl. In a preferred embodiment of the use, in the compounds of Formula I Ra is hydrogen; <br><br> n is 2; <br><br> R^ and R^ are hydrogen; and R5 is -C02H. <br><br> , -N[(CH2)3CH3]2, substituted phenyl, <br><br> -OCH2-substituted phenyl, pyrazolyl, or -N(phenyl)2- <br><br> Rl, R-, and R~ are independently chlorine or hydrogen. <br><br> n is 2; <br><br> R^ and R^ are hydrogen; and <br><br> Also provided is a preferred use of a compound of Formula I <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -14- <br><br> 1 <br><br> wherein <br><br> Ra is hydrogen; <br><br> n is 1 to 5 inclusive; R3 and R^ are hydrogen; <br><br> Rl, R^, and R^ are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -CF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, -N[(CH2)3CH3]2, substituted phenyl, -OCH2~substituted phenyl, pyrazolyl, or -N(phenyl)2; <br><br> R-5 and R^ are independently hydrogen, -CO2H, -NO2, -OCH3, <br><br> rmidazolyl, -CN, fluorine, -CH3, -CF3, or pyrrolyl; <br><br> R^ is COOH or tetrazolyl; <br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for inhibiting the aggregation of amyloid proteins to form amyloid deposits. <br><br> The most preferred compounds provided by the invention have Formula II <br><br> (CH2)n <br><br> II <br><br> COOH <br><br> and pharmaceutically acceptable salts thereof, wherein: <br><br> Rl is halo; <br><br> R^ is H or halo; and <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -15- <br><br> n and R.6 are as defined above in Formula I. <br><br> Another preferred group of compounds have Formula III <br><br> iD <br><br> COOH <br><br> and pharmaceutically acceptable salts thereof, <br><br> wherein: <br><br> Rl is halo; <br><br> is H or halo; and n and are as defined above in Formula I. <br><br> Another group of preferred invention compounds have Formula IV -Rt &gt;==% <br><br> ni r2'^&lt;CHA~V/ ^ <br><br> and pharmaceutically acceptable salts thereof, <br><br> wherein: ' ' , <br><br> I <br><br> Rl is halo; : 2 <br><br> R- is H or halo; and n and R^ are as defined above in Formula I. <br><br> In a preferred embodiment of the use, the novel compounds of Formula I are provided which are <br><br> 2- {4-[2-(3,4-Dichlorophenyl)ethyl]phenylamino} -benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[4-(3,4-Dichloro-phenyl)-ethyI]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> 2-{4-[2-(3,4-Dihydroxy-phenyl)-ethyI]-phenylamino)benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -16- <br><br> 2-{4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino}benzoic acid; 2- {4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino} -4-methoxy-5-nitrobenzoic acid; <br><br> 2- {4- [2- [-(3,4-Dichlorophenyl)propyl]phenylamino} -4-imidazo-1 -yl-5 5-nitrobenzoic acid; <br><br> 2-{4-[2-[-(3,4-Dichlorophenyl)-propyl]phenylamino}benzoic acid; 2-{4-[4-(3,4-Dichlorophenyl)butyl]phenylamino}benzoic acid; 2-{4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamino}-5-nitro-benzoic acid; 2-{4-[4-(3,4-Dichlorophenyl)-butyl]phenylamino}-3,5-dinitrobenzoic <br><br> 0 acid; <br><br> 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino]-benzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid; 2-{4-[2-(3,4-Difluoro-phenyl)-ethyI]-phenylamino}-5-nitro-benzoic acid; 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic <br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid; 2-(4-Phenethyl-phenylamino)-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyIamino}-5-methoxy-benzoic <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-terephthalic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic <br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methanesulfonyl-benzoic acid; <br><br> 30 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-imidazol-l-yl- <br><br> benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-nitro-benzoic acid; 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -4-nitro-benzoic acid; <br><br> acid; <br><br> 20 <br><br> acid; <br><br> 25 <br><br> acid; <br><br> WO 00/76489 <br><br> PCT/USO0/15071 <br><br> acid; acid; <br><br> 10 acid; <br><br> acid; <br><br> -17- <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -3 -nitro-benzoic acid; <br><br> 5-Cyano-2-{4-[2-(3,4-dichloro-phenyI)-ethyl]-phenylamino}-benzoic acid; 2- {4- [2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino } -4,6-difluoro-benzoic <br><br> 6- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -2,3-difluoro-benzoic <br><br> 2- {4- [2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino } -6-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -3-fluoro-benzoic acid; 2- {4- [2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino } -3 -methyl-benzoic <br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -4-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3,5-difluoro-benzoic <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifluoromethyl- <br><br> 15 benzoic acid; <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -6-trifluoromethyl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid; <br><br> 20 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -5-pyrrol-1 -yl-benzoic acid; <br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-(4- {2-[4-(3-Dimethylamino-propoxy)-phenyl]-ethyI} -phenylamino)-benzoic acid; <br><br> 25 2-{4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2- {4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino } -benzoic acid; <br><br> 2-(4-{2-[4-(2-Ethoxy-l-ethoxymethyl-ethyl)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 30 2-{4-[2-(4-Pyrrol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-{4-[2-(4-Styry 1-phenyl)-ethyl] -phenylamino} -benzoic acid; <br><br> 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -18- <br><br> 2- {4-[2-(4'-Ethyl-biphenyl-4-yl)-ethyl] -phenylamino } -benzoic acid; <br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-(4- {2- [3 -(3,5-Dichloro-phenoxy)-phenyl] -ethyl} -phenylamino)-benzoic acid; <br><br> 2-(4-{2-[4-(2-ChIoro-6-fluoro-benzyloxy)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 2-{4-[2-(4-Pyrazol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 2-{4-[2-[(3,4-Dichlorophenyl)propyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl] phenylamino } -5-nitrobenzoic acid; 2-[[4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenyl]amino-benzoic acid; or <br><br> 2-[4-(3,4-Dichlorophenyl)phenyl]aminobenzoic acid. <br><br> The present invention also provides the compounds: <br><br> 2-{4-[4-(3,4-Dichloro-phenyl)-ethyI]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> 2-{4-[2-(3,4-Dihydroxy-phenyl)-ethyl]-phenylamino}benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}benzoic acid; 2-{4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino}benzoic acid; 2-{4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> 2- {4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino} -4-imidazo-1 -yl-5-nitrobenzoic acid; <br><br> 2- {4- [4-(3,4-Dichlorophenyl)butyl]phenylamino} benzoic acid; <br><br> 2- {4- [4-(3,4-Dichloro-phenyl)-butyl] -phenylamino } -5-nitro-benzoic acid; <br><br> 2- {4- [4-(3,4-Dichlorophenyl)-butyl]phenylamino} -3,5-dinitrobenzoic acid; <br><br> 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -19- <br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino]-benzoic acid; 2- {4-[2-(3,4-Dimethyl-phenyl)-ethyl] -phenylamino } -5-nitro-benzoic acid; 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid; 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyI-phenylamino)-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-amino-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichlorophenyl)]phenylamino}-5-nitrobenzoic acid; 2-(4-Phenethyl-phenylamino)-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-terephthalic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic acid; <br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methanesulfonyl- <br><br> benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-imidazol-l-yl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-nitro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-nitro-benzoic acid; 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -3-nitro-benzoic acid; <br><br> 5-Cyano-2- {4-[2-(3,4-dichloro-phenyl)-ethyl]-phenylamino } -benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4,6-difluoro-benzoic acid; <br><br> 6- { 4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -2,3 -difluoro-benzoic acid; <br><br> 2-{4-[2-(3,4-DichIoro-phenyl)-ethyl]-phenylamino}-6-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyI)-ethyl]-phenylamino}-3-fluoro-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -20- <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-methyl-benzoic acid; <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -4-fluoro-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3,5-difluoro-benzoic <br><br> 5 acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifluoromethyl-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-trifluoromethyl-benzoic acid; <br><br> 10 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl- <br><br> benzoic acid; <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -5-pyrrol-1 -yl-benzoic acid; <br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 15 2-(4- { 2-[4-(3-Dimethylamino-propoxy)-phenyl] -ethyl} -phenylamino)- <br><br> benzoic acid; <br><br> 2- {4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino} -benzoic acid; 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 20 2-(4- {2-[4-(2-Ethoxy-1 -ethoxymethyl-ethyl)-phenyl] -ethyl} - <br><br> phenylamino)-benzoic acid; <br><br> 2-{4-[2-(4-Pyrrol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Styryl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; 25 2-{4-[2-(4'-Ethyl-biphenyl-4-yl)-ethyl]-phenylamino}-benzoic acid; <br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[3-(3,5-Dichloro-phenoxy)-phenyl]-ethyl}-phenylamino)-benzoic acid; <br><br> 2-(4-{2-[4-(2-Chloro-6-fluoro-benzyloxy)-phenyl]-ethyl}-phenylamino)-30 benzoic acid; <br><br> 2-{4-[2-(4-Pyrazol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -21- <br><br> 2-(4- {2- [4-(3,4-Dichloro-benzyloxy)-phenyl] -ethyl} -phenylamino)-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-amino-benzoic acid; <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]-phenylamino}-5-trifluoromethyl-benzoic acid; <br><br> 2- {4-[2-(3,4-Dichlorophenyl)]phenylamino } -5-nitrobenzoic acid; 2-{4-[2-[(3,4-Dichlorophenyl)propyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyI]phenylamino}-5-nitrobenzoic acid; 2-{4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenylamino}-benzoic acid; <br><br> 2-{4-[3-(4-Diethylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Nitrophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Nitrophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Aminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Aminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[2-(4-Aminophenyl)ethyl]phenylamino}benzoic acid; 2-{4-[2-(4-Dipropylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride; <br><br> 2-{4-[2-(4-DiethylaminophenyI)ethyl]phenylamino}benzoic acid monohydrochloride monohydrate; <br><br> 2- {4-[3 -(3 -Dipropylaminophenyl)propyl]phenylamino } benzoic acid; 2-{4-[3-(3-Dimethylaminophenyl)propyI]phenylamino}benzoic acid; 2- {4- [3 -(4-Ethylaminophenyl)propyl]phenylamino } benzoic acid; 2-(N-{4-[3-(4-Diethylaminophenyl)propyl]phenyl}-N-ethylamino)benzoic acid; <br><br> 2-{4-[2-(3-Dibenzylaminophenyl)ethyl]phenylamino}benzoic acid; 2- { 4-[3 -(3-Diethylaminophenyl)propyl]phenylamino }benzoic acid; 2- {4- [2-(3-Aminophenyl)ethyl]phenylamino } benzoic acid; 2-{4-[3-(4-Dimethylaminophenyl)propyi]phenyIamino}benzoic acid; 2-{4-[2-(4-Acetylaminophenyl)ethyl]phenylamino} benzoic acid; 2-{4-[2-(3-Acetylaminophenyl)ethyl]phenylamino}benzoic acid; <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -22- <br><br> 2-{4-[2-(3-Dipropylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride; <br><br> 2-{4-[2-(3-Dibutylaminophenyl)ethyl]phenylamino}benzoicacid monohydrochloride; <br><br> 5 2-{4-[3-(4-Acetylaminophenyl)propyl]phenylamino}benzoic acid; <br><br> 2-{4-[3-(3-Acetylaminophenyl)propyl]]phenylamino}benzoic acid; 2-{4-[3-(3-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride; <br><br> 2-{4-[2-(3-Piperidin-l-ylphenyl)ethyl]phenylamino}benzoic acid 10 monohydrochloride; <br><br> 2-{4-[3-(4-Dipropylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Dibutylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-DibutyIaminophenyl)propyl]phenylamino}benzoic acid; 2-(4-{3-[4-(lH-Pyrrol-l-yl)phenyl]propyl}phenyIamino)benzoic acid; 15 2-{4-[3-(4-Piperidin-l-ylphenyl)propyl]phenylamino}benzoic acid; <br><br> 2-{4-[3-(4-Diethylcarbamoylphenyl)propyl]phenylamino}benzoic acid; 2- {4-[3-(4-Carboxyphenyl)propyl]phenylamino } benzoic acid; 2-{4-[3-(4-Diethylaminomethylphenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Propylaminophenyl)propyl]phenylamino}benzoic acid; 20 2-{4-[3-(3-Propylaminophenyl)propyl]phenylamino}benzoic acid; <br><br> 2-{4- [3-(4-Pyrrolidin-1 -yl-phenyl)-propyl]-phenylamino} -benzoic acid; <br><br> 2- {4- [3 -(3 -Piperidin-1 yl-phenyl)-propy l]-phenylamino } -benzoic acid; { 5- [(1 -Butyl-1,2,3,4-tetrahydro-6-quinolyl)methylidene] -4-oxo-2- <br><br> thioxothiazolidin-3-yI} acetic acid; <br><br> 25 { 5-[(l -Butyl-2,3-dihydro-1 H-indol-5-yl)methylidene]-4-oxo-2- <br><br> thioxothiazolidin-3-yl} acetic acid; <br><br> 3-{5-[( 1 -Butyl-1,2,3,4-tetrahydroquinolin-6-yl)methylidene]-4-oxo-2-thioxothiazolidin-3 -yl}propanoic acid; <br><br> 4- { 5-[( 1 -Butyl-1,2,3,4-tetrahydroquinolin-6-yl)methylidene]-4-oxo-2-30 thioxothiazolidin-3-yl}butanoic acid; or <br><br> 2-[4-(3,4-Dichlorophenyl)phenyl]aminobenzoic acid. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -23- <br><br> Also provided are the foregoing compounds wherein the terminal phenylalkyl group is attached at the 2- or 3-position of the central phenyl ring, i.e., compounds of the Formula la <br><br> Typical 2- and 3-substituted compounds are: <br><br> 2- { 3 - [2-(3,4-Dichlorophenyl)ethyl]phenylamino } -benzoic acid; <br><br> 2-{2-[2-(3,4-Dichlorophenyl)ethyl]phenylamino}-benzoic acid; <br><br> 2- {3 - [3-(4-Diethylaminophenyl)propyl]phenylamino} -benzoic acid; <br><br> 2- {3-[3 -(4-Di-n-propylaminophenyl)propyl]phenylamino} -benzoic acid; <br><br> 2- {3 -[3-(4-n-Propylaminophenyl)propyl]phenylamino} -benzoic acid; <br><br> 2-{3-[3-(4-[2-Diethylaminoethylamino]phenyl)propyl]phenylamino}-benzoic acid; <br><br> 2-{2-[3-(4-[Hydroxycarbonylmethylamino]phenyl)propyl]phenylamino}-benzoic acid; <br><br> 2- {2- [2-(3 - [2-Diethylaminoethylamino]phenyl)ethyl]phenylamino } -benzoic acid; <br><br> 2- { 3 -[3 -(4-Morpholinophenyl)propyl]phenylamino}-benzoic acid; <br><br> 2- {3-[3-(4-Piperazinylphenyl)propyl]phenylamino} -benzoic acid; <br><br> 2-{3-[2-(4-Chlorophenyl)ethyl]phenylamino}-benzoicacid; <br><br> 2- {3-[3-(3,4-Dichlorophenyl)propyl]phenylamino }-benzoic acid; and <br><br> 2-{4-[4-(4-{4-Methylpiperazinyl}phenyl)butyl]phenylamino}-benzoic <br><br> Pharmaceutical formulations of the novel compounds admixed with a pharmaceutically acceptable diluent, carrier, or excipient are also provided. <br><br> Also provided is a method of imaging amyloid deposits, the method comprising: <br><br> la acid. <br><br> WO 00/76489 <br><br> PCT/USO0/15O71 <br><br> -24- <br><br> a. introducing into a patient a detectable quantity of a labeled compound having the Formula I or a pharmaceutically acceptable salt thereof: <br><br> 10 <br><br> 15 <br><br> 20 <br><br> 7^==/ R4 F <br><br> -R <br><br> R <br><br> wherein <br><br> O <br><br> Ra is hydrogen, Cj-Cg alkyl, or -CCj-Cg alkyl; <br><br> n is 0 to 5 inclusive; <br><br> Rl, R^, r3, r4} r5} r65 ^ r7 are independently hydrogen, <br><br> halogen, -OH, -NH2, NRbRc, -C02H, -C02Ci-C6 alkyl, -N02, -OCj-C12 alkyl, -Ci-C8 alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyI, -O-phenyl, -O-substituted phenyl, <br><br> O O <br><br> II I <br><br> -CH=CH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C i -C6alkyl)(CH2)pNRbRc, <br><br> /CH20CrC6 alkyl <br><br> —CH \ <br><br> CH2OCrC6 alkyl <br><br> R^ is COOH, tetrazolyl, -S02Rd, or -C0NHS02Rd; <br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m- <br><br> phenyl, or Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-C]-C6 <br><br> WO 00/76489 <br><br> PCT/US00/1S071 <br><br> -25- <br><br> alkylpiperazinyl, morpholino, thiomorpholino, decahydroisoquinoline, or pyrazolyl; <br><br> Rd is hydrogen, -C^-Cg alkyl, -CF3, or phenyl; <br><br> m is 0 to 5 inclusive; <br><br> p is 1 to 5 inclusive; <br><br> A is CH or N; <br><br> Rl and R^, when adjacent to one another, can be methylene-dioxy; or the pharmaceutically acceptable salts thereof; <br><br> b. allowing sufficient time for the labeled compound to become associated with amyloid deposits; and c. detecting the labeled compound associated with the amyloid deposits. <br><br> In a preferred embodiment of the method, the patient has or is suspected to have Alzheimer's disease. <br><br> In a preferred embodiment of the method, the labeled compound is a radio labeled compound. <br><br> In a preferred embodiment of the method, the labeled compound is detected using MRI. <br><br> The present invention also provides the preferred compounds: <br><br> 2- {4- [2-(3,4-Dichlorophenyl)ethyl]pheny lamino } -benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid; 2-{4-[3-(3,4-Dichlorophenyl)-propyl]phenylamino}benzoic acid; 2-[[4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenyl]amino-benzoic acid; <br><br> 2- {4-[3-(4-Diethylaminophenyl)propyl]phenylamino } -benzoic acid; and pharmaceutical formulations thereof. <br><br> Pharmaceutically acceptable acid addition salts, amides, and prodrugs of the foregoing compoimds are also provided by this invention. <br><br> 10 <br><br> 15 <br><br> ® 20 <br><br> 25 <br><br> WO 00/76489 PCT/US00/15071 <br><br> -26- <br><br> DETAILED DESCRIPTION OF THE INVENTION <br><br> The term "alkyl" means a straight or branched chain hydrocarbon having from 1 to 12 carbon atoms. Representative examples of alkyl groups are methyl, ethyl, propyl, isopropyl, isobutyl, butyl, tert-butyl, sec-butyl, pentyl, hexyl, octyl, decyl, and 1,1-dimethyloctyl. <br><br> Preferred alkyl groups are Cj-Cg alkyl, and especially Cj-Cg alkyl. <br><br> The term "alkoxy" means an alkyl group attached to an oxygen atom. Representative examples of alkoxy groups include methoxy, ethoxy, tert-butoxy, propoxy, and isobutoxy. Preferred alkoxy groups are C i -C j 2 alkoxy, and especially C\-C$ alkoxy. <br><br> The term "halogen" includes chlorine, fluorine, bromine, and iodine. <br><br> The term "substituted" means that one or more hydrogen atom in a molecule has been replaced with another atom or group of atoms. For example, substituents include halogen, especially chloro, -OH, -CF3, -NO2, -NH2, -NH(C 1 -Cgalkyl), -N^-Cgalkyl^, Ci-C6 alkyl, -OC]-C6 alkyl, -CN, -CF3, -CO2H, and -C02Cj-C6 alkyl. <br><br> The term "substituted phenyl" means a phenyl ring in which from 1 to 4 hydrogen atoms have been independently replaced with a substituent, preferably one selected from the list above. Typical "substituted phenyl" groups include 4-chIorophenyl, 3,4-dibromophenyl, 3-fluoro-4-methylphenyl, <br><br> 3,4-dichlorophenyl, 3,4-methylenedioxyphenyl, and 4-dimethylaminophenyl. <br><br> The symbol"-" means a covalent bond. <br><br> Substituent groups represented by Rl, r3, and R^, for example, include amino(NRbRc) and acylamino (-NHCORb). Rb and Rc can be hydrogen, alkyl and phenylalkyl and substituted phenylalkyl, and typical NRbRc groups include methylamino, diethylamino, isobutyl-propylamino, benzylamino, and 3,4-dimethoxybenzylamino. Examples of acylamino groups include formamido, acetamido, 2-phenylacetamido, and 2-(3-nitrophenyl)acetamido. R', R^, <br><br> and R5 can also be aminoalkoxy (-0(CH2)pNRbRc) such as N-methylaminomethoxy and 2-(N-benzylamino)ethoxy, as well as <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -27- <br><br> aminoalkylamino (-NH(CH2)pNRbRc) such as 3-(dimethylamino)propylamino and 2-(N-ethyl-N-benzylamino)ethylamino. Substituent groups such as R*, R^, and R^ additionally can be cyclic structures, for instance when NRbRc is part of the substituent group, and Rb and Rc are taken together with the nitrogen to which 5 they are attached to form a cyclic ring selected from imidazole, pyrrole, <br><br> piperidine, piperazine, 4-Cj-Cg alkylpiperazine, moipholine, thiomorpholine, <br><br> pyrazole, and decahydroisoquinoline. <br><br> Substituent groups such as R^, R^, r5? r6? and R^ also can be -CH=CH-phenyl (i.e., styryl), phenoxy, O-substituted phenyl such as 3-iodophenoxy, 2,4,6-10 trihydroxyphenoxy, 2-fluoro-3-nitrophenoxy, as well as -O-benzyl and <br><br> -O-substituted benzyl such as 2-trifluoromethylbenzyloxy and 4-aminobenzyloxy. <br><br> The term "pharmaceutically acceptable salt, ester, amide, and prodrug" as used herein refers to those carboxylate salts, amino acid addition salts, esters, amides, and prodrugs of the compounds of the present invention which are, within 15 the scope of sound medical judgement, suitable for use in contact with the tissues of patients without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term "salts" refers to the relatively nontoxic, inorganic and organic 20 acid addition salts of compounds of the present invention. These salts can be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free base form with a suitable organic or inorganic acid and isolating the salt thus formed. Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate, 25 oxalate, valerate, oleate, palmitate, stearate, laureate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate mesylate, glucoheptonate, lactobionate and laurylsulphonate salts, and the like. These may include cations based on the alkali and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium, and the like, as well as, 30 nontoxic ammonium, quaternary ammonium and amine cations including, but not limited to ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like. (See, for <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -28- <br><br> example, Berge S.M., et al., Pharmaceutical Salts, J. Pharm. Set., 66:1-19 (1977) which is incorporated herein by reference.) <br><br> Examples of pharmaceutically acceptable, nontoxic esters of the compounds of this invention include Cj-Cg alkyl esters wherein the alkyl group is a straight or branched chain. Acceptable esters also include C5-C7 cycloalkyl esters as well as arylalkyl esters such as, but not limited to benzyl. C j -C4 alkyl esters are preferred. Esters of the compounds of the present invention may be prepared according to conventional methods, for example by reacting a carboxylic acid of Formula I with an alcohol such as ethanol or benzyl alcohol. <br><br> Examples of pharmaceutically acceptable, nontoxic amides of the compoimds of this invention include amides derived from ammonia, primary Cj-Cg alkyl amines and secondary Cj-Cg dialkyl amines wherein the alkyl groups are straight or branched chain. In the case of secondary amines, the amine may also be in the form of a 5- or 6-membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C1-C3 alkyl primary amides and C4-C2 dialkyl secondary amides are preferred. Amides of the compounds of the invention may be prepared according to conventional methods. <br><br> The term "prodrug" refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formulas, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems. Vol. 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference. <br><br> In addition, the compounds of the present invention can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the present invention. <br><br> The compounds of the present invention can exist in different stereoisometric forms by virtue of the presence of asymmetric centers in the compounds. It is contemplated that all stereoisometric forms of the compounds, as well as mixture thereof, including racemic mixtures, form part of this invention. <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -29- <br><br> In the first step of the present method of imaging, a labeled compound of Formula I is introduced into a tissue or a patient in a detectable quantity. The compound is typically part of a pharmaceutical composition and is administered to the tissue or the patient by methods well-known to those skilled in the art. <br><br> The compound can be administered either orally, rectally, parenterally (intravenous, by intramuscularly or subcutaneously), intracisternally, intravaginally, intraperitoneally, intravesically, locally (powders, ointments or drops), or as a buccal or nasal spray. <br><br> Compositions suitable for parenteral injection may comprise physiologically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, and sterile powders for reconstitution into sterile injectable solutions or dispersions. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents, or vehicles include water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants. <br><br> These compositions may also contain adjuvants such as preserving, wetting, emulsifying, and dispensing agents. Prevention of the action of microorganisms can be ensured by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, and the like. It may also be desirable to include isotonic agents, for example sugars, sodium chloride, and the like. Prolonged absorption of the injectable pharmaceutical form can be brought about by the use of agents delaying absorption, for example, aluminum monostearate and gelatin. <br><br> Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is admixed with at least one inert customary excipient (or carrier) such as sodium citrate or dicalcium phosphate or (a) fillers or extenders, as for example, starches, lactose, sucrose, glucose, mannitol, and silicic acid; (b) binders, as for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidone, sucrose, and acacia; (c) humectants, as for example, glycerol; (d) disintegrating agents, as for <br><br> WO 00/76489 PCT/US00/15071 <br><br> -30- <br><br> example, agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, <br><br> certain complex silicates and sodium carbonate; (e) solution retarders, as for example paraffin; (f) absorption accelerators, as for example, quaternary ammonium compounds; (g) wetting agents, as for example, cetyl alcohol and 5 glycerol monostearate; (h) adsorbents, as for example, kaolin and bentonite; and (i) lubricants, as for example, talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, or mixtures thereof. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents. <br><br> Solid compositions of a similar type may also be employed as fillers in 10 soft- and hard-filled gelatin capsules using such excipients as lactose or milk sugar, as well as high molecular weight polyethyleneglycols, and the like. <br><br> Solid dosage forms such as tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells, such as enteric coatings and others well known in the art. They may contain opacifying agents, and can also be of such 15 composition that they release the active compound or compounds in a certain part of the intestinal tract in a delayed manner. Examples of embedding compositions which can be used are polymeric substances and waxes. The active compounds can also be in microencapsulated form, if appropriate, with one or more of the above-mentioned excipients. <br><br> 20 Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art, such as water or other solvents, solubilizing agents and emulsifiers, as for example, ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, 25 benzyl alcohol, benzyl benzoate, propyleneglycol, 1,3-butyleneglycol, <br><br> dimethylformamide, oils, in particular, cottonseed oil, groundnut oil, corn germ oil, olive oil, castor oil, and sesame oil, glycerol, tetrahydrofurfuryl alcohol, polyethyleneglycols, and fatty acid esters of sorbitan or mixtures of these substances, and the like. <br><br> 30 Besides such inert diluents, the composition can also include adjuvants, <br><br> such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents. <br><br> WO 00/76489 PCT/USO0/15071 <br><br> -31- <br><br> Suspensions, in addition to the active compounds, may contain suspending agents, as for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, <br><br> bentonite, agar-agar and tragacanth, or mixtures of these substances, and the like. <br><br> 5 Compositions for rectal administrations are preferably suppositories which can be prepared by mixing the compounds of the present invention with suitable nonirritating excipients or carriers such as cocoa butter, polyethyleneglycol or a suppository wax, which are solid at ordinary temperatures but liquid at body temperature and therefore, melt in the rectum or vaginal cavity and release the 10 active component. <br><br> Dosage forms for topical administration of a compound of this invention include ointments, powders, sprays, and inhalants. The active component is admixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers or propellants as may be required. Ophthalmic formulations, 15 eye ointments, powders, and solutions are also contemplated as being within the scope of this invention. <br><br> In a preferred embodiment of the invention, the labeled compound is introduced into a patient in a detectable quantity and after sufficient time has passed for the compound to become associated with amyloid deposits, the labeled 20 compound is detected noninvasively inside the patient. In another embodiment of the invention, a labeled compound of Formula I is introduced into a patient, sufficient time is allowed for the compound to become associated with amyloid deposits, and then a sample of tissue from the patient is removed and the labeled compound in the tissue is detected apart from the patient. In a third embodiment 25 of the invention, a tissue sample is removed from a patient and a labeled compound of Formula I is introduced into the tissue sample. After a sufficient amount of time for the compound to become bound to amyloid deposits, the compound is detected. <br><br> The administration of the labeled compound to a patient can be by a 30 general or local administration route. For example, the labeled compound may be administered to the patient such that it is delivered throughout the body. Alternatively, the labeled compound can be administered to a specific organ or tissue of interest. For example, it is desirable to locate and quantitate amyloid <br><br> WO 00/76489 PCT/USOO/15071 <br><br> -32- <br><br> deposits in the brain in order to diagnose or track the progress of Alzheimer's disease in a patient. <br><br> The term "tissue" means a part of a patient's body. Examples of tissues include the brain, heart, liver, blood vessels, and arteries. A detectable quantity is 5 a quantity of labeled compound necessary to be detected by the detection method chosen. The amount of a labeled compound to be introduced into a patient in order to provide for detection can readily be determined by those skilled in the art. For example, increasing amounts of the labeled compound can be given to a patient until the compound is detected by the detection method of choice. A label is 10 introduced into the compoimds to provide for detection of the compounds. <br><br> The term "patient" means humans and other animals. Those skilled in the art are also familiar with determining the amount of time sufficient for a compound to become associated with amyloid deposits. The amount of time necessary can easily be determined by introducing a detectable amount of a 15 labeled compound of Formula I into a patient and then detecting the labeled compound at various times after administration. <br><br> The term "associated" means a chemical interaction between the labeled compound and the amyloid deposit. Examples of associations include covalent bonds, ionic bonds, hydrophilic-hydrophilic interactions, hydrophobic-20 hydrophobic interactions, and complexes. <br><br> Those skilled in the art are familiar with the various ways to detect labeled compounds. For example, magnetic resonance imaging (MRI), positron emission tomography (PET), or single photon emission computed tomography (SPECT) can be used to detect radiolabeled compounds. The label that is introduced into the 25 compound will depend on the detection method desired. For example, if PET is selected as a detection method, the compound must possess a positron-emitting atom, such as He or 18p. <br><br> Another example of a suitable label in a compound of Formula I is an atom such as 13c, l^N, or l^F which can be detected using magnetic resonance 30 imaging (MRI) which is also sometimes called nuclear magnetic resonance <br><br> (NMR). In addition, the labeled compounds of Formula I may also be detected by MRI using paramagnetic contrast agents. <br><br> WO 00/76489 <br><br> PCI7USO0/15071 <br><br> o&gt; <br><br> Another example of detection is electron paramagnetic resonance (EPR). In this case, EPR probes which are well-known in the art, such as nitroxides, can be used. <br><br> The imaging of amyloid deposits can also be carried out quantitatively so that the amount of amyloid deposits can be determined. <br><br> The present invention also provides a use of a compound of Formula I in the manufacture of a medicament for inhibiting the aggregation of amyloid proteins to form amyloid deposits. Those skilled in the art are readily able to determine an amyloid inhibiting amount by simply administering a compound of Formula I to a patient in increasing amounts until the growth of amyloid deposits is decreased or stopped. The rate of growth can be assessed using imagining or by taking a tissue sample from a patient and observing the amyloid deposits therein. <br><br> A patient in need of inhibition of the aggregation of amyloid proteins is a patient having a disease or condition in which amyloid proteins aggregate. Examples of such diseases and conditions include Mediterranean fever, Muckle-Wells syndrome, idiopathetic myeloma, amyloid polyneuropathy, amyloid cardiomyopathy, systemic senile amyloidosis, amyloid polyneuropathy, hereditary cerebral hemorrhage with amyloidosis, Alzheimer's disease, Down's syndrome, Scrapie, Creutzfeldt-Jacob disease, Kuru, Gerstmann-Straussler-Scheinker syndrome, medullary carcinoma of the thyroid, Isolated atrial amyloid, [^-microglobulin amyloid in dialysis patients, inclusion body myositis, <br><br> P2-amyloid deposits in muscle wasting disease, and Islets of Langerhans diabetes Type II insulinoma. <br><br> Also provided by the present invention are compounds of Formula I wherein one or more atom in the compound has been replaced with a radioisotope <br><br> (a labeled compound). The radioisotope can be any radioisotope. However,^H, 123^ 125131 js 1 1q and 18p ^ preferred. Those skilled in the art are familiar with the procedure used to introduce a radioisotope into a compound. For example, a compound of Formula I wherein one carbon atom is or I4C is readily prepared. <br><br> The compounds of the present invention can be administered to a patient at dosage levels in the range of about 0.1 to about 1,000 mg per day. For a normal human adult having a body weight of about 70 kg, a dosage in the range of about 0.01 to about 100 mg per kilogram of body weight per day is sufficient. The specific dosage used, however, can vary. For example, the dosage can depend on a number of factors including the requirements of the patient, the severity of the condition being treated, and the pharmacological activity of the compound being used. The determination of optimum dosages for a particular patient is well-known to those skilled in the art <br><br> Unless the context clearly requires otherwise, throughout the description and the claims, the words "comprise", "comprising" and the like, are to be construed in an inclusive sense as opposed to an exclusive or exhaustive sense, <br><br> that is to say, in the sense of "including, but not limited to". <br><br> The examples presented below are intended to illustrate particular embodiments of the invention and are not intended to limit the scope of the specification, including the claims, in any manner. <br><br> EXAMPLES" ! 2 <br><br> SYNTHESIS <br><br> Compounds of Formula I can be prepared by several routes as illustrated in Schemes 6 through 9. Schemes 1 through 5 show synthetic routes that can be used to obtain the desired starting amines (IV), (VIII), (XV), and (XXI). <br><br> In Scheme 1, the appropriately substituted aldehyde (I) and a nitrophenylacetic acid (II) yield olefin (III) when heated inpiperidine at 150°C. Standard hydrogenation conditions, such as Raney nickel, give desired amine (IV). <br><br> Scheme 2 depicts the synthesis of amine (VIII) which contains a three methylene tether. Condensation of aldehyde (I) and nitro-ketone (V) in the presence of sodium hydroxide gives the desired alpha, beta-unsaturated ketone, which upon standard hydrogenation conditions (Raney nickel) gives (VII) and then Wolff-Kishner conditions yields the desired amine (VIII). <br><br> Scheme 3 is very similar to Scheme 2, except that the aldehyde (I) is condensed with a substituted aniline (IX). <br><br> Scheme 4 illustrates standard Wittig conditions in which the starting materials (XII) and (XIII) are obtained via aldol condensation and ylide chemistry, respectively. Reaction of aldehyde (XII) and bromophosphorane (XIII) in the <br><br> WO 00/76489 PCT/US00/15071 <br><br> -35- <br><br> presence of a base, such as butyl lithium, gives diene (XIV). Standard reduction conditions (e.g., Raney nickel) of (XIV) yields the desired amine (XV). <br><br> Scheme 5 illustrates the synthesis of amine (XXI) which contains a 5-methylene tether. Wittig reaction of the bromophosporane (XVII), which is 5 formed from the corresponding substituted bromide (XVI), and nitro aldehyde (XIX), obtained from Swern oxidation of the corresponding alcohol (XVIII), <br><br> using a base (e.g., LHDMS) yields olefin (XX). Reduction of (XX) using standard conditions (Raney nickel) gives amine (XXI). <br><br> Scheme 6 illustrates one route to obtain compounds of Formula I. Either 10 by Buchwald coupling (Method A) followed by saponification or utilizing the Ullman reaction (Method B), compounds of Formula I can be isolated from amines such as (IV), (VIII), and (XV). Compounds of Formula I that contain hydroxy groups, such as Examples 4 and 6, require demethylation of the hydroxy protecting groups with reagents such as boron tribromide in the final step of the 15 synthesis. <br><br> Protecting groups will also be used when reactive functional groups such as amino and carboxylic acids are present, so as to avoid unwanted side reactions. Carboxy groups typically are converted to esters (e.g., tert-butyl, benzyl), and amino groups generally are acylated (e.g., acetyl or trimethylsilyl). These and 20 other such protecting groups are well-known to organic chemists, and are fully described by Greene and Wuts in Protective Groups in Organic Synthesis. John Wiley and Sons, New York (2nd Ed. 1991). All citations are incorporated herein by reference. <br><br> Scheme 7 illustrates the synthesis of compounds of Formula I by reacting 25 amines such as (IV), (VIII), and (XXI) with fluoro-nitro intermediate (XXIV), in the presence of a base (e.g., LHMDS or Et3N) to give ester (XXV). This ester can then be saponified using standard conditions, such as sodium hydroxide. <br><br> In Scheme 8, amine (XV) can be coupled with readily available fluoro-substituted carboxylic acids [e.g., (XXVI) or (XXVII)] in the presence of various 30 bases (such as DBU or triethylamine) to yield compounds of Formula I. <br><br> Scheme 9 depicts coupling of amine (VIII) with readily available methyl ester (XXVIII) in the presence of a base, such as imidazole, to give ester (XXIX). <br><br> WO 00/76489 PCT/US00/15071 <br><br> -36- <br><br> This ester can then be saponified as usual to give compounds of Formula I. <br><br> Scheme 10 illustrates the synthesis of fluoro-intermediate (XXIV) which is obtained by nitration of readily available methyl ester (XXX) to give (XXVIII). Treatment of (XXVIII) with potassium cyanide gives (XXIV). <br><br> 5 In Scheme 11, the synthesis of compounds related to Example 18 is illustrated. Reaction of the potassium salts of ortho-substituted benzoic acids (XXVI) with substituted anilines (XXVII) in the presence of potassium carbonate and cupric acetate yields various iodo-substituted aminobenzoic acids (XXVIII). Reaction of (XXVIII) with substituted boronic acids and palladium chloride gives 10 the desired substituted aminobenzoic acids (XXX). <br><br> It should, of course, be recognized that several invention compoimds of Formula I can be prepared from other compounds defined by Formula I, utilizing standard organic reactions such as oxidation, reduction, alkylation, condensation, elimination, and similar well-known synthetic processes. For example, 15 compounds of Formula I wherein Ra is hydrogen are readily alkylated to form compounds wherein Ra is Cj-Cg alkyl. Compounds wherein R* is NH2 are readily acylated by reaction with an acid halide or acid anhydride to provide compounds wherein R' is -NHCORb. Similarly, compounds wherein R^ is N02 are easily reduced to provide compounds wherein R* is NH2. The benzoic acids <br><br> 20 (where R^ is COOH) are readily converted to esters and amides, as well as salts and other prodrugs by routine processes. For example, the benzoic acid can be reacted with oxalylchloride to form the acid chloride, which then readily reacts with a sulfonamide such as methanesulfonamide to produce the corresponding invention compound where R** is -C0NHS02CH3- <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> Formation of Amines <br><br> -37- <br><br> Scheme 1 <br><br> R2 __R7 <br><br> R <br><br> y—CHO + H00c, <br><br> (I) <br><br> (II) <br><br> -NO-, <br><br> Step A Piperidine _ ^2 <br><br> 150°C, 5b <br><br> R /=\ <br><br> ,1' <br><br> (in) <br><br> Step B <br><br> / <br><br> Ra-Ni/THFor Pd-C/DMF <br><br> -NO, <br><br> R?_^=\,R7 /=\ <br><br> R <br><br> /J <br><br> /) nh2 <br><br> (IV) <br><br> Scheme 2 <br><br> -CHO + H3C^V \ N0. <br><br> (d <br><br> (vm) <br><br> Step A' R' NaOH(aq) EtOH <br><br> (V) <br><br> Wolff-Kischner reaction Nh2 Step C' <br><br> (VII) <br><br> NOi <br><br> NHo <br><br> WO 00/76489 PCT/US00/15071 <br><br> -38-Scheme 3 <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -39- <br><br> Scheme 4 <br><br> R <br><br> R^==wR7 (I) <br><br> CH3CHO <br><br> NO, <br><br> Br (XI) <br><br> P(Ph)3 <br><br> R1 &gt; f CHO+Br(Ph)3P <br><br> (XII) (XIII) <br><br> NQ2 n-BuLi/THF <br><br> (XIV) <br><br> Ra-Ni <br><br> THF/MeOH <br><br> NH- <br><br> (XV) <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -40- <br><br> Scheme 5 <br><br> \v&gt;/==V^'A\ <br><br> (XVI) <br><br> R1 PPh.Br <br><br> (xvn) <br><br> 0H DMSO,(COCl)2 <br><br> (xvin) <br><br> H2N~\ a <br><br> (XXI) <br><br> R <br><br> Ra-Ni/H2 1 THF <br><br> 0-.N <br><br> LHDMS THF <br><br> '2N—\ // <br><br> (XX) <br><br> CHO <br><br> Rx <br><br> R7 <br><br> ^R1 <br><br> Coupling Routes <br><br> Scheme 6 <br><br> Method A. Step C (l)Pd2(dba)3/BINAP Cs2COj, toluene <br><br> (XXIII) <br><br> WO 00/76489 PCT/US00/15071 <br><br> -41-Scheme 7 <br><br> 2 r7 n=0,l, 3 <br><br> NB <br><br> (iv), (vm), (xxi) <br><br> R <br><br> 2 F <br><br> "N02 (a) LHDMS, THF <br><br> or (b) CH3CN COOR Et3N, reflux <br><br> (XXTV) <br><br> R~ <br><br> COOH <br><br> Compound of Formula I <br><br> R is an ester forming group such as alkyl or benzyl. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -42- <br><br> Scheme 8 <br><br> COOH <br><br> COOH <br><br> (xxvn) <br><br> Compound of Formula I <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -43- <br><br> Scheme 9 <br><br> nh2 + f <br><br> (V m) <br><br> NOo <br><br> H ,N. <br><br> COOMe <br><br> (xxvni) <br><br> o <br><br> N—^ <br><br> ch3cn <br><br> Et^N, reflux <br><br> COOH <br><br> Compound of Formula i <br><br> Synthesis of Fluoro-Intermediate <br><br> Scheme 10 <br><br> (xxx) (xxvm) (xxiv) <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -44- <br><br> Scheme 11 <br><br> COOK <br><br> Br KjCOj/MeOH <br><br> (XXV) <br><br> (XXVI) (XXVE) <br><br> COOH <br><br> (XXVIII) <br><br> CI (XXIX) <br><br> K2C03, PdCl2dppfCH2Cl2 Dioxane <br><br> COOH <br><br> (XXX) <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -45-EXAMPLE 1 <br><br> Preparation of 2-{4-[2-(3,4-Dichlorophenyl)ethyl]phenylamino}-benzoic acid <br><br> Step A (Scheme 1): Preparation of l,2-Dichloro-4-[2-(4-nitrophenyl)ethenyl]-benzene <br><br> 5 A mixture ofp-nitrophenylacetic acid (51.23 g, 0.28 mol) and <br><br> 3,4-dichlorobenzaldehyde (49.50 g, 0.28 mol) in piperidine (50 mL) was heated to 150-160°C for 5 hours under a N2 atmosphere. After cooling the reaction mixture, <br><br> the precipitate was triturated in boiling methanol (MeOH) (50 mL) and then cooled to -5°C for 12 hours. The crystalline precipitate was filtered off, rinsed 10 with cold MeOH and dried at room temperature in a vacuum oven overnight to yield an orange solid, 22.71 g (0.077 mol, 27%) of the desired product, mp 190-191°C. <br><br> MS-.294.9 (M+). <br><br> Step B (Scheme 1): Preparation of 4-[2-(3,4-DichIorophenyl)ethyl]benzenamine 15 A sample of l,2-dichloro-4-[2-(4-nitrophenyl)ethenyl]benzene (98.0 g, <br><br> 0.33 mol) in tetrahydrofuran (THF) (1.6 L) was reduced in the presence of Raney Nickel (Ra-Ni) (20 g) at 25°C to 40°C (AP =13.5 psi) under a hydrogen atmosphere. The reaction mixture was filtered, and the filtrate was concentrated in vacuo to give an orange solid, 85.0 g (0.32 mol, 95.8%) of the desired product. 20 mp 68-70°C. <br><br> MS: 266.1 (M+). <br><br> Step C (Scheme 6): Preparation of <br><br> 2-{4-[2-(3,4-Dichlorophenyl)ethyl]phenylamino}-benzoic acid Method A <br><br> 25 A mixture of 4-[2-(3,4-dichlorophenyl)ethyl]benzenamine (28.37 g, <br><br> 106.59 mmol), methyl 2-bromobenzoate (19.10 g, 88.82 mmol), cesium carbonate (40.52 g, 124.35 mmol), tris(dibenzylideneacetone-dipaladium(0) (2.44 g, 2.67 mmol) and (5}-(2,2'-bis(di-p-tolylphosphino-l,r-binaphthyl (98%, (S)-toI-BINAP) (2.71 g, 4.00 mmol) (Ligand/Pd = 1.5) in anhydrous toluene (300 mL) <br><br> WO 00/76489 PCT/US00/15071 <br><br> -46- <br><br> was heated to 100°C for 34 hours under N2. After cooling to room temperature, the reaction mixture was diluted with ether, filtered through celite and rinsed thoroughly with ether. The filtrate was evaporated to dryness to give a brown residue (68 g). The resulted residue was dissolved in ethanol (EtOH) (50 mL) and 5 THF (100 mL), and then 5N NaOH (aq.) (200 mL) was added, and the mixture was refluxed for 16 hours. The solvent was removed in vacuum. The residue was acidified with concentrated HC1 to pH 3. The resulting precipitate was collected by filtration, triturated with boiling MeOH-H20 (4:1) and dried in a vacuum at room temperature for 16 hours to give Example 1, an orange solid (31.95 g, 10 0.083 mol, 77.6%). mp 175.0-177.0°C. <br><br> Analysis for C2iH17N102Cl2: Calcd: C, 65.30; H, 4.44; N, 3.63. <br><br> Found: C, 65.40; H, 4.54; N, 3.50. <br><br> Method B <br><br> A mixture of 2-chlorobenzoic acid (5.4 g, 0.034 mol), 4-[2-(3,4-15 dichlorophenyl)ethyl]benzenamine (10.0 g, 0.037 mol), anhydrous potassium carbonate (16.9 g, 0.12 mol), copper powder (4.94 g, 0.077 mol), and copper(I) chloride (0.37 g, 0.0037 mol) in dry dimethylformamide (DMF) (85 mL) was heated to reflux for 24 hours at 150°C. The reaction mixture was poured into hot H20 (150 mL) and heated to 90°C on a hot plate. Charcoal was added, and this 20 mixture was stirred at 90°C for 5 minutes. The warm brown mixture was filtered through filter paper. The cooled filtrate was then acidified with concentrated HC1 (pH 1), and the precipitate was collected by filtration, triturated with boiling Me0H-H20 (1:2) and dried under vacuum at room temperature for 16 hours to give Example 1, an orange solid (2.3 g, 0.006 mol, 17.5%). mp 165.0-173.0°C. 25 Analysis for C21H17N1O2CI2: Calcd: C, 65.30; H, 4.44; N, 3.63. <br><br> Found: C, 65.68; H, 4.58; N, 3.60. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -47-EXAMPLE 2 <br><br> Preparation of 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino } -5-nitrobenzoic acid <br><br> Step C (Scheme 6): Preparation of 2-{4-[2-(3,4-Dichloro-phenyl)-5 ethyljphenylamino} -5-nitrobenzoic acid methyl ester <br><br> A mixture of 4-[2-(3,4-dichlorophenyI)ethyl]benzenamine (600 mg, 2.25 mmol), 2-bromo-5-nitrobenzoic acid methyl ester (489 mg, 1.88 mmol), cesium carbonate (857 mg, 2.62 mmol), tris(dibenzylideneacetone-dipaladium(0) (51 mg, 0.056 mmol) and (5)-(2,2'-bis(di-p-tolylphosphino-1,1 '-binaphthyl (98%, 10 (S)-tol-BINAP) (58 mg, 0.085 mmol) (Ligand/Pd = 1.5) in anhydrous toluene <br><br> (16 mL) was heated to 100°C for 12 hours under N2- After cooling, the reaction mixture was diluted with ether, filtered through celite and rinsed thoroughly with ether. The filtrate was evaporated to dryness to give a brown residue. Purification by flash chromatography (silica gel, 5% EtOAc/hexane) yielded 540 mg 15 (1.21 mmol, 64%) of the desired product, mp 107-108°C. <br><br> Analysis for C22Hi8N2Cl204: Calcd: C, 59.34; H, 4.07; N, 6.29. <br><br> Found: C, 59.03; H, 4.04; N, 5.99. <br><br> Preparation of 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid <br><br> 20 A solution of 2-{4-[2-(3,4-dichloro-phenyl)-ethyl]phenylamino}- <br><br> 5-nitrobenzoic acid methyl ester (340 mg, 0.76 mmol) and IN NaOH (aq.) (4.0 mL) in EtOH (4.0 mL) and THF (4.0 mL) was heated to reflux for 16 hours. The solvent was removed in vacuum. The residue was diluted with H2O and acidified with concentrated HC1 to pH 1. The mixture was then extracted with 25 methylene chloride, dried (Na2SC&gt;4), filtered and concentrated in vacuo to yield a yellow solid, 329 mg (0.76 mmol, 100%) of the desired product, mp 214-217°C. Analysis for C2iH16N2Cl204: Calcd: C, 58.49; H, 3.74; N, 6.50. <br><br> Found: C, 58.24; H, 3.81; N, 6.28. <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -48-EXAMPLE 3 <br><br> Preparation of 2- {4-[4-(3,4-Dichloro-phenyl)-ethyl]phenylamino } -4-methoxy-5-nitrobenzoic acid <br><br> To a cooled (-78°C) solution of 4-[2-(3,4-dichloro-phenyl)-ethyl]phenylamine (0.836 g, 3.14 mmol) in THF (20 mL), LHDMS (6.28 mL, 1 M in THF, 6.28 mmol) was added dropwise. The reaction mixture was allowed to stir at -78°C for 10 minutes. A solution of 2-flouro-4-methoxy-5-nitrobenzoic acid methyl ester (0.72 g, 3.14 mmol) in THF (30 mL) was added dropwise, and this solution was stirred for 30 minutes at -78°C. The reaction mixture was allowed to gradually warm to room temperature and stir for 2 hours under a N2 atmosphere. The reaction mixture was diluted with ethyl acetate (EtOAc), and acidified with 5N HC1 (pH 3). The organic layer was dried (Na2S04), filtered and concentrated in vacuo to yield a brown residue. To a solution of this residue in EtOH (20 mL) and THF (40 mL), 5N NaOH (50 mL) was added, and the mixture was refluxed for overnight. The solvent was removed in vacuum, and the residue was acidified with concentrated HC1 (pH 3). The precipitate was collected by filtration, <br><br> triturated with boiling Me0H-H20 (1:1), and dried in a vacuum oven for 16 hours to give Example 3, an orange solid (0.70 g, 1.51 mmol, 48%). mp 208-209°C. Analysis for C22H18N205C12: Calcd: C, 57.28; H, 3.93; N, 6.07. <br><br> Found: C, 57.43; H, 3.69; N, 5.86. <br><br> EXAMPLE 4 <br><br> Preparation of 2-{4-[2-(3,4-Dihydroxy-phenyl)-ethyl]-phenylamino}benzoic acid <br><br> Step A (Scheme 1): Preparation of l,2-Dimethoxy-4-[2-(4-nitrophenyl)ethenyl]-benzene <br><br> The title compound was prepared from j9-nitrophenylacetic acid (25.0 g, 0.14 mol), and 3,4-dimethoxybenzaldehyde (21.0 g, 0.14 mol) in piperidine (5 mL) using the procedure described in Example 1, Step A, to yield a yellow solid, 13.4 g (0.047 mol, 34%) of the desired product, mp: 133-134°C. <br><br> Analysis of CjgH^NjC^: Calcd: C, 67.36; H, 5.30; N, 4.91. Found: C, 66.81; H, 5.27; N, 4.84. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -49- <br><br> Step B (Scheme 1): Preparation of 4-[2-(3,4-Dimethoxy-phenyl)ethyl]-phenylamine l,2-Dimethoxy-4-[2-(4-nitrophenyl)ethenyl]benzene (12.1 g, 0.042 mol) was reduced in the presence of 10% Pd-C (2.0 g) in dimethylformamide (DMF) (120 mL) at 25°C under a hydrogen atmosphere. The reaction mixture was concentrated in vacuo to give a solid. The solid was recrystallized from MeOH (400 mL) to yield a white crystalline product, 6.8 g (0.026 mol, 63%) of the desired product, mp 115-116°C. <br><br> Analysis for C]6Hi9Nj02: Calcd: C, 74.68; H, 7.44; N, 5.44. Found: C, 74.60; H, 7.39; N, 5.35. <br><br> Step C (Scheme 6): Preparation of 2-{4-[2-(3,4-Dimethoxy-phenyl)ethyl]-phenylamino}benzoic acid <br><br> The title compound was prepared from 4-[2-(3,4-dimethoxy-phenyl)-ethyl]phenylamine (9.25 g, 0.036 mol), 2-chlorobenzoic acid (5.2 g, 0.036 mol), anhydrous potassium carbonate (15.0 g, 0.11 mol), copper powder (0.45 g, 0.007 mol), and a catalytic amount of copper(I) chloride in dry DMF (75 mL) using the procedure described in Example 1, Step C, Method B. After crystallization with Me0H/H20,4.5 g (0.012 mol, 33%) of the desired product was obtained, mp: 137-139°C. <br><br> Analysis for C23H23N1O4: Calcd: C, 73.19; H, 6.14; N, 3.71. Found: C, 73.47; H, 6.03; N, 3.78. <br><br> Step D: Preparation of 2-{4-[2-(3,4-Dihydroxy-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> To a solution of 2-{4-[2-(3,4-dimethoxy-phenyl)-ethyl]phenylamino}-benzoic acid (0.28 g, 0.74 mmol) in CH2Cl2 (20 mL), BBr3 (3.5 mL, 1M in CH2Cl2, 3.5 mmol) was added at room temperature under a N2 atmosphere. The reaction mixture was allowed to stir at room temperature for 2 hours and then poured into ice water (50 mL). This mixture was extracted with EtOAc, and the organic layer was washed two times with water, dried (Na2S04), filtered and <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -50- <br><br> concentrated in vacuo to yield 0.24 g (0.69 mmol, 93%) of the desired product, mp 215-217°C. <br><br> Analysis for C21H19NO4: Calcd: C, 72.19; H, 5.48; N, 4.00. Found: C, 71.80; H, 5.46; N, 3.99. <br><br> EXAMPLE 5 <br><br> Preparation of 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}benzoic acid <br><br> Step A (Scheme 1): Preparation of l,l-Dibutylamino-4-[2-(4-nitrophenyl)ethenyl]benzene <br><br> The title compound was prepared from/j-nitrophenylacetic acid (9.92 g, 0.055 mol) and 4-dibutylamino-benzaldehyde (14.32 g, 0.055 mol) in piperidine (5 mL) using the procedure described in Example 1, Step A. This procedure yielded a red solid, 4.12 g (0.012 mol, 16%) of the desired product. <br><br> MS: 352.2. (M+); 353.2. (MH+). <br><br> Step B (Scheme 1): Preparation of 4-[2-(4,4-Dibutylaminophenyl)ethyl]-phenylamine <br><br> The title compound was prepared from l,l-dibutylamino-4-[2-(4-nitrophenyl)ethenyl]benzene (4.10 g, 11.63 mmol) and Ra-Ni (2.0 g) in MeOH (100 mL) at 21°C to 32°C (AP = 3.6 psi) under a hydrogen atmosphere using the procedure described in Example 1, Step B. This procedure yielded a colorless oil, 3.49 g (10.76 mmol, 92.6%) of the desired product. <br><br> MS: 325.3 (MH+). <br><br> Step C (Scheme 6): Preparation of 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}-benzoic acid <br><br> The title compound was prepared from 2-chIorobenzoic acid (1.46 g, 9.36 mmol), 4-[2-(4,4-dibutylaminophenyl)ethyl]phenylamine (3.31 g, 10.20 mmol), anhydrous potassium carbonate (4.27 g, 30.88 mmol), copper powder (1.25 g, 19.65 mmol), and copper(I) chloride (0.092 g, 0.93 mmol) in dry DMF (30 mL) using the procedure described in Example 1, Step C, Method B. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -51- <br><br> This procedure yielded a 0.39 g (0.87 mmol, 8.6%) of the desired product, mp 115-117°C. <br><br> Analysis for C29H36N2O2: Calcd: C, 78.34; H, 8.16; N, 6.30. Found: C, 78.15; H, 8.07; N, 6.10. <br><br> EXAMPLE 6 <br><br> Preparation of 2-{4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino}benzoic acid <br><br> Step A (Scheme 1): Preparation of l,2,3-Trimethoxy-5-[2-(4-nitrophenyl)ethenyl]benzene <br><br> The title compound was prepared from p-nitrophenylacetic acid (18.6 g, 0.10 mol), 3,4,5-trimethoxy-benzaldehyde (19.6 g, 0.10 mol) and piperidine (5 mL) using the procedure described in Example 1, Step A. This procedure yielded a solid, 13.0 g (0.041 mol, 41%) of the desired product. mp:192-195°C. <br><br> Step B (Scheme 1): Preparation of 4-[2-(3,4,5-Trimethoxy-phenyl)ethyl]-phenylamine <br><br> The title compound was prepared from l,2,3-trimethoxy-5-[2-(4-nitrophenyl)ethenyl]benzene (9.5 g, 0.03 mol) and Ra-Ni (1.0 g) in THF (50 mL) at 21-26°C (AP = 9.6 psi) under a hydrogen atmosphere using the procedure described in Example 1, Step B. This procedure yielded a tan powder, 6.6 g (0.023 mol, 74%) of the desired product, mp 91-93°C. <br><br> Step C (Scheme 6): Preparation of 2-{4-[2-(3,4,5-Trimethoxy-phenyl)-ethyl]phenylamino}-benzoic acid methyl ester <br><br> The title compound was prepared from 4-[2-(3,4,5-trmethoxyphenyl)-ethyljphenylamine (0.75 g, 2.61 mmol), methyl 2-bromobenzoate (0.47 g, 2.17 mmol), cesium carbonate (0.99 g, 3.04 mmol), tris(dibenzylideneacetone-dipaladium(O) (0.06 g, 0.065 mmol) and (5)-(-0-2,2'-bis(di-p-tolylphosphino-1,1'-binaphthyl (98% (S)-Tol-BINAP) (0.066 g, 0.098 mmol) (Ligand/Pd = 1.5) in anhydrous toluene (100 mL) using the procedure described in Example 1, Step C, Method A to yield a yellow oil, 0.69 g (1.63 mmol, 76%) of the desired product. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -52- <br><br> Analysis for 025^7^05: Calcd: C, 71.24; H, 6.46; N, 3.32. Found: C, 71.53; H, 6.24; N, 3.14. <br><br> Preparation of 2- {4-[2-(3,4,5-Trimethoxy-phenyl)ethyl]phenylamino} -benzoic acid <br><br> 5 To a solution of 2-{4-[2-(3,4,5-trimethoxyphenyl)ethyI]phenylamino}- <br><br> benzoic acid methyl ester (0.62 g, 1.47 mmol) in THF-EtOH (2:1, 6 mL), IN NaOH solution (4 mL) was added, and the reaction mixture was heated to reflux for 5 hours. The reaction mixture was then concentrated in vacuo to remove the organic solvent. The residue was acidified with concentrated HC1 (pH 3). This 10 precipitate was collected by filtration, triturated with boiling Me0H-H20 (4:1) and dried in vacuum at room temperature for 16 hours to give the title compound as a white solid, 0.59 g (1.45 mmol, 98.5%). mp 146.0-147.0°C. <br><br> Analysis for 024^5^05: Calcd: C, 70.75; H, 6.18; N, 3.44. Found: C, 70.54; H, 6.43; N, 3.15. <br><br> 15 Step D: Preparation of 2-{4-[2-(3,4,5-Trihydroxyphenyl)ethyI]phenylamino}-benzoic acid <br><br> The title compound was prepared from 2-{4-[2-(3,4,5-trimethoxy-phenyl)' ethyl]phenylamino}benzoic acid (0.50 g, 1.23 mmol) in CH2Cl2 (40 mL) and BBrj (10 mL, 1M in CH2CI2, 10.0 mmol) using the procedure described in 20 Example 4, Step D. This procedure yielded a green solid, 0.25 g (0.68 mmol, 65%) of the desired product, mp: 160.0-162.0°C. <br><br> Analysis for C21H19N1O5-I.44 H2O: Calcd: C, 64.46; H, 5.64; N, 3.58. <br><br> Found: C, 64.07; H, 5.27; N, 3.39. <br><br> EXAMPLE 7 <br><br> 25 Preparation of 2- {4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino} -4-methoxy-5-nitrobenzoic acid <br><br> WO 00/76489 PCT/US00/15071 <br><br> -53- <br><br> Step A' (Scheme 2): Preparation of 3-(3,4-Dichlorophenyl)-l-(4-nitro-phenyl)propenone <br><br> Sodium hydroxide (7.3 g, 0.18 mol) was dissolved in water (80 mL) and 95% EtOH (80 mL) and cooled to 10°C with an ice-H20 bath. <br><br> 5 3,4-Dichlorobenzaldehyde (31.8 g, 0.18 mol) was added in one portion. After the addition, the mixture was wanned to 15°C. l-(4-Nitrophenyl)ethanone (30.0 g, 0.18 mol) was added at this temperature with rigorous stirring. After stirring for 5 minutes, the reaction mixture was diluted with 95% EtOH (300 mL). The resulting tan mixture was stirred at room temperature for 30 minutes, then stirred 10 with an ice-H20 bath underneath the flask for 2 hours. The light brown solid was filtered off, washed with H2O, and air-dried. The solid was dissolved in hot THF (1.5 L) and treated with charcoal. The resulting mixture was filtered off, and the filtrate was diluted with 95% EtOH (500 mL). This solution was filtered and oven-dried (40°C) to yield a light brown solid, 38.56 g (0.12 mol, 66%) of the title 15 compound, mp 220-223°C. <br><br> Analysis for C15H9Cl2N03: Calcd: C, 55.93; H, 2.82; CI, 22.01; N, 4.35. <br><br> Found: C, 55.79; H, 2.93; CI, 22.16; N, 4.32. <br><br> Step B' (Scheme 2): Preparation of l-(4-Amino-phenyl)-3-(3,4-dichloropheny l)propan-1-one 20 3-(3,4-Dichlorophenyl)-l-(4-nitro-phenyl)propenone (34.56 g, 0.11 mol) <br><br> was reduced in the presence of Ra-Ni (3.0 g) in THF (250 mL) at 20°C to 32°C (AP = 33.4 psi) under a hydrogen atmosphere. The reaction mixture was concentrated in vacuo and recrystallized from MeOH (100 mL) to give a light yellow solid, 23.5 g (0.080 mol, 75%) of the desired product, mp 127-129°C. 25 Analysis for C15H13CI2NO: Calcd: C, 61.24; H, 4.45; N, 4.76; CI, 24.10. <br><br> Found: C, 60.91; H, 4.60; N, 4.70; CI, 23.98. <br><br> Step C' (Scheme 2): Preparation of 4-[3-(3,4-Dichlorophenyl)propyl]phenylamine <br><br> A mixture of 1 -(4-aminophenyl)-3-(3,4-dichlorophenyl)propan-1 -one (20.0 g, 0.068 mol), NH2NH2-H2O (16 mL), and KOH (85%, 5.6 g) in ethylene <br><br> WO 00/76489 PCT/US00/15071 <br><br> -54- <br><br> glycol (160 mL) was heated to reflux under a N2 atmosphere for 16 hours. After cooling to room temperature, the reaction mixture was poured into ice-H20 and extracted with CH2CI2 (2 L). The layers were separated, and the organic layer was dried (Na2SC&gt;4) and concentrated in vacuo to afford an oil. Purification by 5 flash chromatography (silica gel, CH2CI2) yielded an oil,14.00 g (0.05 mol, 73%) of the desired product. <br><br> Analysis for C15H15Cl2N: Calcd: C, 64.30; H, 5.40; N, 4.99; CI, 25.31. <br><br> Found: C, 64.21; H, 5.59; N, 5.24; CI, 24.87. <br><br> Preparation of 2,4-Difluoro-5-nitrobenzoic acid methyl ester 10 Fuming nitric acid 90% (8.5 mL, 0.19 mol) was added with gentle stirring to concentrated sulfuric acid 98% (125 mL) in a 1 L beaker. After stirring for 10 minutes at room temperature, 2,4-difluorobenzoic acid methyl ester (21.9 g, 0.127 mol) was added dropwise. After the addition, the reaction mixture was allowed to stir gently for 40 minutes at room temperature. The reaction mixture 15 was then poured into ice-H20 (1 L) and stirred for 10 minutes. The mixture was extracted with EtOAc. The layers were separated, and the organic layer was washed sequentially with IN NaCl, saturated NaHCC&gt;3, H2O and brine, dried (Na2SC&gt;4), filtered and concentrated in vacuo to afford a yellow residue. This residue was washed with 10% EtOAc/hexane, filtered, and dried to yield a pale 20 yellow solid, 29.0 g (0.133 mol, 82%). mp 78-80°C. <br><br> Analysis for C8H5F2NC&gt;4: Calcd: C, 44.25; H, 2.32; N, 6.45. Found: C, 44.18; H, 2.39; N, 6.14. <br><br> Preparation of 2-Fluoro-4-methoxy-5-nitrobenzoic acid methyl ester <br><br> A mixture of sodium metal (1.27 g, 0.055 mol) and MeOH ( 250 mL) was 25 stirred at 0°C for 10 minutes. This solution was added to a solution of 2-fluoro-5- <br><br> nitrobenzoic acid methyl ester (10.0 g, 0.046 mol) in MeOH (250 mL), and the mixture was stirred for 20 minutes at 0°C to 5°C. The reaction mixture was then allowed to warm to room temperature and stir for 2 hours. The mixture was then filtered to give an off-white precipitate. Recrystallization with CHCI3 (70 mL) <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -55- <br><br> yielded an off-white crystalline solid, 1.825 g (0.008 mol, 17%) of the title compound. <br><br> Analysis for C9H8F1N1O5: Calcd: C, 47.17; H, 3.52; N, 6.11. Found: C, 47.09; H, 3.47; N, 6.00. <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid methyl ester <br><br> A mixture of 4-[3-(3,4-dichloro-phenyl)propyl]phenylamine (0.94 g, 3.3 mmol), 2-fluoro-4-methoxy-5-nitro-benzoic acid methyl ester (0.75 g, 3.3 mmol), and Et3N (0.46 mL) in'Ct^CN (30 mL) was heated to reflux for 120 hours. The reaction mixture was cooled to room temperature, diluted with CH2CI2 and washed with saturated NaHCC&gt;3. The organic layer was dried (Na2SC&gt;4) and concentrated to give a solid. Recrystallization with MeOH yielded 0.67 g (1.37 mmol, 42%) of the desired product. <br><br> Analysis for C24H22N2Cl205-0.42H20: Calcd: C, 58.01; H, 4.63. N, 5.64; Found: C, 57.61; H, 4.51; N, 5.94. <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid <br><br> To a solution of 2-{4-[3-(3,4-dichlorophenyI)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid methyl ester (0.30 g, 0.061 mol) in THF (5 mL), IN NaOH (aq.) (2.5 mL) was added, and the mixture was stirred for 36 hours at room temperature. The solvent was removed, and the residue was acidified with concentrated HC1 to pH 3. The precipitate was collected by filtration and dried in vacuum for 16 hours. Recrystallization with MeOH gave the title compound as an orange solid 0.21 g (0.043 mol, 70%). mp 200-201°C. <br><br> Analysis for C23H2oN205Cl2-0.2H20: Calcd: C, 57.68; H, 4.29; N, 5.85; CI, 14.81. Found: C, 57.71; H, 4.34; N, 5.58; CI, 14.56. <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -56-EXAMPLE 8 <br><br> Preparation of 2-{4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino}-4-imidazo-l-yl-5-nitrobenzoic acid <br><br> Preparation of 2- {4-[2-[-(3,4-Dichlorophenyl)propyl]phenylamino} -4-imidazo-l-yl-5-nitrobenzoic acid methyl ester <br><br> A mixture of 2,4-difluoro-5-nitrobenzoic acid methyl ester (1.63 g, 7.5 mmol), imidazole (0.56 g, 8.25 mmol), and Et3N (1.14 mL, 8.25 mmol) in CH3CN (50 mL) was stirred for 16 hours at room temperature. To this deep orange solution, 4-[3-(3,4-dichlorophenyl)propyl]phenylamine (2.10 g, 7.5 mmol) and triethylamine (Et3N) (1.14 mL, 8.25 mmol) was added, and the mixture was heated to reflux for overnight. The reaction mixture was cooled and concentrated in vacuo to afford a residue. This residue was diluted with CH2CI2 and washed with a saturated K.2HC03 solution. The organic layer was dried (Na2S04), filtered, and concentrated in vacuo to give a crude oil. Purification by flash chromatography (silica gel, 10% EtOAc/hexane) yielded 1.0 g (1.90 mmol, 25%) of the desired product. <br><br> MS: 524.1 (M+). <br><br> Preparation of 2- {4- [2- [-(3,4-Dichlorophenyl)propyl]phenylamino} -4-imidazo-l-l-yl-5-nitrobenzoic acid <br><br> The title compound was prepared from 2-{4-[2-[-(3,4-dichlorophenyl)propyl]phenylamino } -4-imidazo-1 -yl-5 -nitrobenzoic acid methyl ester (1.0 g, 1.9 mmol), IN NaOH (2.0 mL) in THF (30 mL) using the procedure described in Example 8. This procedure yielded an orange solid, 0.30 g (0.6 mmol, 32%) of the desired product. <br><br> Analysis for C25H2oCl2N404-0.2H20: Calcd: C, 58.31; H, 3.99; N, 10.88; CI, 13.89. Found: C, 58.34; H, 4.07; N, 10.73; CI, 13.41. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -57-EXAMPLE 9 <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)-propyl]phenylamino}-benzoic acid <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-benzoic acid methyl ester <br><br> 5 The title compound was prepared from 4-[3-(3,4-dichlorophenyl)propyl]- <br><br> phenylamine (600 mg, 2.14 mmol), 2-bromobenzoic acid methyl ester (380 mg, 1.78 mmol), cesium carbonate (812 mg, 2.49 mmol), tris(dibenzylideneacetone-dipaladium(O) (49 mg, 0.053 mmol) and (S)-(2,2'-bis(di-p-tolylphosphino-l,r-binaphthyl (98%, (S)-tol-BINAP) (54 mg, 0.080 mmol) (Ligand/Pd = 1.5) in 10 anhydrous toluene (15 mL) using the procedure described in Example 2, Step C. This procedure yielded an yellow oil, 0.61 g (1.47 mmol, 69%) of the desired product. <br><br> MS: 414 (M+), 416 (MH+). <br><br> Analysis for C23H2iCl2O2N-0.4 H20: Calcd: C, 65.25; H, 5.23; N, 3.30. 15 Found: C, 65.76; H, 5.18; N, 3.10. <br><br> Preparation of 2- {4- [3-(3,4-Dichlorophenyl)propyl]phenylamino} -benzoic acid <br><br> The title compound was prepared from 2-{4-[3-(3,4-dichlorophenyl)-propyl]phenylamino}benzoic acid methyl ester (0.41 g, 0.99 mmol), INNaOH (4.0 mL) in EtOH (4 mL) and THF (4 mL) using the procedure described in 20 Example 2. This procedure yielded a yellow solid, 0.32 g (0.80 mmol, 81%) of the desired product, mp 120-126°C. <br><br> Analysis for C22Hi9Cl2O2Nr0.75 H20: Calcd: C, 64.04; H, 5.00; N, 3.39. Found: C, 64.17; H, 4.69; N, 3.18. <br><br> EXAMPLE 10 <br><br> 25 Preparation of 2-{4-[4-(3,4-Dichlorophenyl)butyl]phenylamino}benzoic acid <br><br> Preparation of (/ra«.s)-3-(3,4-Dichlorophenyl)-2-propenal <br><br> A mixture of 3,4-dichlorobenzaldehyde (140.0 g, 0.8 mol) and acetaldehyde (300 mL) was cooled to 5°C. Potassium hydroxide (5.1 g, <br><br> 0.091 mol) was dissolved in hot MeOH (40 mL), and the resulting solution was <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -58- <br><br> added to the above cooled mixture while maintaining the internal temperature at 25°C to 30°C. The mixture was allowed to stir in ice-H20 bath for 40 minutes and then treated with acetic anhydride (400 mL). After the addition, the mixture was heated to 100°C with stirring for 30 minutes and then cooled to 30°C. To this 5 mixture, 12N HCI/H2O (102 mL/1.2 L) was added, and the resulting mixture was heated to reflux for 30 minutes and then cooled to room temperature. This heterogeneous mixture was filtered and washed with H2O to afford a brown solid. The crude product was dissolved in EtOAc and washed with H20, dried (Na2SC&gt;4), and concentrated to dryness. Recrystallization from hexane/EtOAc 10 (9:1) yielded 76.5 g (0.38 mol, 48%) of the title compound, mp: 91-93°C. <br><br> Analysis for C9H6C120: Calcd: C, 53.77; H, 3.01; CI, 35.27. Found: C, 53.75; H, 3.10; CI, 35.58. <br><br> Preparation of (trans), (trans)-1,2-Dichloro-4-[4-(4-nitrophenyl)-1,3-butadienyl]benzene <br><br> 15 A mixture of 4-nitro-benzyl bromide (200.0 g, 0.93 mol) and triphenylphosphine (244.0 g, 0.93 mol) in CHCI3 (1.5 L) was heated to reflux for overnight. The reaction mixture was cooled to room temperature, concentrated in vacuo to remove CHCI3 and then suspended in Et20 and stirred rigorously. The suspension was filtered, and the off-white solid was washed with Et20, dried 20 at 80°C for 16 hours to give 433.0 g (0.91 mol, 98%) of bromo[(4-nitrophenyl)methyl]triphenylphosphorane .A solution of bromo[(4-nitrophenyl)methyl]triphenylphosphorane (100.0 g, 0.23 mol) in dry THF (500 mL) was cooled to 5°C. n-Butyl lithium (n-BuLi) (2.4 M, 96 mL, 0.23 mol) was added dropwise to maintain the temperature between 5°C to 10°C. The 25 cooling bath was then removed, and the reaction mixture was allowed to warm to room temperature. After 4 hours, a solution of (trans)-3-(3,4-dichlorophenyl)-2-propenal (36.2 g, 0.18 mol) in THF (100 mL) was added dropwise, and the resulting mixture was stirred at room temperature for 16 hours. The mixture was filtered, and the filtrate was concentrated in vacuo to give a residue. Purification <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -59- <br><br> by flash chromatography (silica gel, 20% EtOAc/hexane) yielded 16.0 g (0.05 mol, 28%) of the desired product, mp 125-135°C. <br><br> Analysis for C^Hi 1CI2NO2: Calcd: C, 60.02; H, 3.46; N, 4.37, CI, 22.15. <br><br> Found: C, 59.77; H, 3.47; N, 4.40; CI, 22.39. <br><br> Preparation of 4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamine <br><br> The title compound was prepared from (trans), (trans)-1,2-dichloro-4-[4-(4-nitrophenyl)-l,3-butadienyl]benzene (15.42 g, 0.048 mol), Ra-Ni (1 g) at 20°C to 26°C (AP = 19.3 psi) under a hydrogen atmosphere in THF (75 mL) and MeOH (75 mL) using the procedure described in Example 1, Step B. This procedure yield a solid, 10.97 g (0.037 mol, 78%) of the desired product, mp 50-52°C. <br><br> Analysis of C^H^N^: Calcd: C, 65.32; H, 5.82; N, 4.76. Found: C, 65.43; H, 5.84; N, 4.61. <br><br> Preparation of 2-{4-[4-(3,4-Dichlorophenyl)butyl]phenylamino}benzoic acid <br><br> The title compound, mp 98-105°C, was prepared from 4-[4-(3,4-dichlorophenyl)butyl]phenylamine (0.50 g, 1.7 mmol), 2-chlorobenzoic acid (0.24 g, 1.56 mmol), anhydrous potassium carbonate (0.71 g, 5.15 mmol), copper powder (0.21 g, 3.28 mmol), and copper(I) chloride (0.015 g, 0.15 mmol) in dry DMF (5 mL) using the procedure described in Example 1, Step C, Method B. <br><br> EXAMPLE 11 <br><br> Preparation of 2-{4-[4-(3,4-Dichloro-phenyl)-butyI]-phenylamino}-5-nitro-benzoic acid <br><br> A mixture of 2-fluoro-5-nitrobenzoic acid (1.85 g, 0.01 mol), 4-[4-(3,4-dichlorophenyl)butyl]-phenylamine (2.94 g, 0.01 mol) and Et3N (2.80 mL) in acetonitrile (110 mL) was heated to reflux for 48 hours. The reaction mixture was cooled and concentrated in vacuo to remove the solvent. The residue was dissolved in CH2Cl2 and washed with diluted HC1. The organic layer was dried (Na2S04), concentrated in vacuo to give a crude solid. Purification by flash <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -60- <br><br> chromatography (silica gel, CH2CI2) yielded 1.40 g (0.003 mol, 30%) of the desired product. <br><br> Analysis for C23H19N2O4CI2: Calcd: C, 60.27; H, 4.18; N, 6.11; CI, 14.47. Found: C, 60.16; H, 4.41; N, 6.09; CI, 15.69. <br><br> 5 EXAMPLE 12 <br><br> Preparation of 2-{4-[4-(3,4-Dichlorophenyl)-butyl]phenylamino}-3,5-dinitrobenzoic acid <br><br> To a cooled (0°C) solution of 4-[4-(3,4-dichlorophenyl)butyl]-phenylamine (1.47 g, 5.0 mmol) and DBU (0.75 mL, 7.5 mmol) in acetonitrile 10 (25 mL), a solution of 2-fluoro-2,5-dinitrobenzoic acid (1.15 g, 5.0 mmol) in acetonitrile (15 mL) was added dropwise. After stirring for 30 minutes at 0°C, the reaction mixture was neutralized with dilute HCl and extracted with EtOAc, dried (Na2SC&gt;4), filtered and concentrated in vacuo to afford a crude residue. <br><br> Recrystallization with EtOH yielded a bright orange solid, 2.06 g (4.1 mmol, 15 82%) of the title compound. <br><br> Analysis for C23H19Cl2N306: Calcd: C, 54.77; H, 3.80; N, 8.33; CI, 14.06. Found: C, 54.68; H, 4.00; N, 8.12; CI, 13.81. <br><br> EXAMPLE 13 <br><br> Preparation of 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic 20 acid <br><br> Preparation of Bromo[(3,4-dichlorophenyl)methyl]triphenylphosphorane <br><br> A mixture of 4-bromomethyl-l,2-dichlorobenzene (2.40 g, 0.01 mol), and triphenylphosphine (5.24 g, 0.02 mol) in toluene (30 mL) was stirred for 16 hours at room temperature. The solid was filtered, rinsed with toluene, and oven-dried at 25 room temperature to yield a white powder, 3.95 g (0.0078 mol, 78%) of the desired product. <br><br> *HNMR [dimethylsulfoxide (DMSO):ppm] :7.89-7.61 (m, 15H), 7.50 (d, .7=8.3 Hz, 1H), 7.04 (t, J= 2.3 Hz, 1H), 6.97 (m, 1H), 5.20 (d, .7=15.9 Hz, 2H). <br><br> WO 00/76489 PCT/US00/15071 <br><br> -61- <br><br> Preparation of 4-(4-Nitrophenyl)butyraldehyde <br><br> To a cooled solution (-70°C) of oxalyl chloride (2.0 M in CH2CI2, <br><br> 14.1 mL, 28.2 mmol), dimethylsulfoxide (DMSO) (4.40 g, 56.32 mmol) in CH2CI2 (20 mL) was added dropwise. The resulting reaction mixture was then <br><br> 5 stirred for 30 minutes at -70°C under a nitrogen atmosphere. A solution of <br><br> 4-(4-nitrophenyl)butan-l-ol (5.00 g, 25.6 mmol) in CH2CI2 (3 mL) was added dropwise, and the reaction mixture was stirred for 1 hour at -70°C. Et3N (16 mL, <br><br> 115 mmol) was added, and the reaction mixture was then allowed to gradually warm to room temperature and stir for 30 minutes. The mixture was then 10 quenched with H2O and extracted with EtOAc. The organic layers were washed with 0.1N HCl solution, H2O, brine, dried (Na2S04), filtered, and concentrated in vacuo to give a lightly brown oil. Purification by flash chromatography (silica gel, 50% EtOAc/hexane) yielded 3.20 g (16.56 mmol, 65%) of the desired product. <br><br> 15 *H NMR (DMSO:ppm): 9.75 (s, 1H), 8.12 (d, .7=8.3 Hz, 2H), 7.30 (d, 7=8.3 Hz, 2H), 2.72 (t, J= 7.7 Hz, 2H), 2.47 (t, J=l. 1 Hz, 2H), 1.94 (m, 2H). <br><br> Preparation of l,2-Dichloro-4-[5-(4-nitrophenyl)-l-pentenyl]benzene <br><br> A solution of bromo[(3,4-dichlorophenyl)methyl]triphenylphosphorane (3.95 g, 7.9 mmol) in dry THF (20 mL) was cooled to 0°C. LHDMS (1.0 M/THF, 20 9 mL, 9.0 mol) was added dropwise to maintain the temperature at 0°C. After stirring for 30 minutes, a solution of 4-(4-nitro-phenyl)butyraldehyde (1.45 g, 7.5 mmol) in THF (5 mL) was added dropwise, and the mixture was allowed to warm to room temperature within 2 hours. The mixture was then quenched with H2O and extracted with EtOAc. The organic layers were washed with 0.1N HCl 25 solution, H2O, brine, dried (Na2S04), filtered, and concentrated in vacuo to give a lightly brown oil. Purification by flash chromatography (silica gel, 10% EtOAc/hexane) yielded 2.5 g (7.4 mmol, 99%) of the desired product. MS: 335 (M+), 337 (MH+). <br><br> WO 00/76489 PCT/US00/15071 <br><br> -62- <br><br> Preparation of 4-[5-(3,4-Dichlorophenyl)pentyl]phenylamine <br><br> The title compound was prepared from l,2-dichloro-4-[5-(4-nitrophenyl)-l-pentenyl]benzene (2.5 g, 7.4 mmol), Ra-Ni (1 g) in THF (50 mL) at 25°C to 40°C (AP = 9.9 psi) using the procedure described in Example 1, Step B. This 5 procedure yielded 1.06 g (3.4 mmol, 46%) of the desired product. <br><br> *H NMR (DMSO:ppm): 7.45 (d, ^=8.3 Hz, 1H), 7.41 (d, J= 2.2 Hz, 1H), 7.12 (m, 1H), 6.74 (d, .7=8.3 Hz, 2H), 6.40 (d, J=8.3 Hz, 2H), 4.73 (s, 2H), 2.50 (t, J=7.7 Hz, 2H), 2.31 (t, .7=7.6 Hz, 2H), 1.6-1.5 (m, 4H), 1.5-1.4 (m, 2H). <br><br> Preparation of 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-5-nitrobenzoic 10 acid <br><br> To a cooled (-78°C) solution of 4-[5-(3,4-dichlorophenyl)pentyl]-phenylamine (0.231 g, 0.75 mmol) in THF (2 mL), LHDMS (2.25 mL, 1 M in hexane, 2.25 mmol) was added dropwise. The reaction mixture was allowed to stir at -78°C for 10 minutes. A solution of 2-fluoro-5-nitrobenzoic acid (0.139 g, 15 0.75 mmol) in THF (2 mL) was added dropwise, and this solution was stirred for <br><br> 30 minutes at -78°C. The reaction mixture was allowed to gradually warm to room temperature and stir for 2 hours under N2 atmosphere. The reaction mixture was diluted with EtOAc, and acidified with IN HCl (pH 3). The organic layer was dried (Na2S04), filtered and concentrated in vacuo to yield a brown residue. 20 Purification by flash chromatography (silica gel, 2% MeOH/CH2Cl2) then recrystallization with MeOH yielded 265 mg (0.56 mmol, 75%) of the desired product, mp 147-148°C. <br><br> Analysis for C24H22C12N204-0.37H20: Calcd: C, 60.05; H, 4.77; N, 5.84. <br><br> Found: C, 59.67; H, 4.64; N, 5.51. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -63-EXAMPLE 14 <br><br> Preparation of2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid <br><br> Preparation of 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid methyl ester <br><br> The title compound was prepared from 4-[5-(3,4-dichlorophenyl)pentyl]phenylamine (231 mg, 0.75 mmol), LHDMS (6.28 mL, 1 M in THF, 6.28 mmol) and 2-fluoro-4-methoxy-5-nitrobenzoic acid methyl ester (172 g, 0.75 mmol) in THF (5 mL) using the procedure described in Example 13. Purification by flash chromatography (silica gel, 10% EtOAc/hexane) yielded 145 mg (0.28 mmol, 37%) of the desired product. <br><br> MS: 515.2 (M+), 517.2 (MH+). <br><br> Preparation of 2- {4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino }-4-methoxy-5-nitrobenzoic acid <br><br> The title compound was prepared from 2-{4-[5-(3,4-dichlorophenyl)-pentyI]phenylamino}-4-methoxy-5-nitrobenzoic acid methyl ester (145 mg, 0.28 mmol) and IN NaOH (aq.) (0.56 mL) in THF (1.2 mL) using the procedure described in Example 2. Purification by flash chromatography (silica gel, 10% MeOH/CH2Cl2), then recrystallization with MeOH yielded 58 mg (0.12 mmol, 41 %) of the desired product, mp 192-193°C. <br><br> Analysis for C25H24C12N205: Calcd: C, 59.65; H, 4.81; N, 5.56. <br><br> Found: C, 59.29; H, 4.58; N, 5.36. <br><br> EXAMPLE 15 <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-5-nitrobenzoic acid <br><br> Preparation of 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-5-nitrobenzoic acid methyl ester <br><br> The title compound was prepared from 4-[3-(3,4-dichlorophenyl)propyl]-phenylamine (420 mg, 1.50 mmol), 2-bromobenzoic acid methyl ester (310 mg, <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -64- <br><br> 1.25 mmol), cesium carbonate (569 mg, 1.75 mmol), tris(dibenzylideneacetone-dipaladium(O) (34 mg, 0.037 mmol) and (5)-(2,2'-bis(di-p-tolylphosphino-l,r-binaphthyl (98%, (S)-tol-BINAP) (38 mg, 0.056 mmol) (Ligand/Pd=1.5) in anhydrous toluene (15 mL) using the procedure described in Example 2, Step C. This procedure yielded an orange solid 0.51 g (1.11 mmol, 74%) of the desired product, mp 117-118°C. <br><br> MS: 457.1 (M+); 459.1 (MH+) <br><br> Preparation of 2- {4-[3 -(3,4-Dichlorophenyl)propyl]phenylamino} -5-nitrobenzoic acid <br><br> The title compound was 2-{4-[3-(3,4-dichlorophenyl)-propyl]phenylamino}-5-nitrobenzoic acid methyl ester (0.50 g, 1.09 mmol), 2N NaOH (5.0 mL) in EtOH (2 mL) and THF (4 mL) using the procedure described in Example 2. This procedure yielded an orange solid, 0.49 g (1.10 mmol, 100%) of the desired product, mp 153-155°C. <br><br> MS: 443.2 (M+), 445.2 (MH+) <br><br> EXAMPLE 16 <br><br> Preparation of 2- {4-[2-(3,4-Dimethyl-phenyl)-ethyl]phenylamino } -5-nitrobenzoic acid <br><br> Preparation of 2- {4-[2-(3,4-Dimethyl-phenyl)-ethyl]phenylamino} -5-nitrobenzoic acid methyl ester <br><br> The title compound was prepared from 4-[2-(3,4-dimethylphenyl)ethyl]-benzenamine (1.0 g, 4.43 mmol), 2-bromo-5-nitrobenzoic acid methyl ester (0.96 g, 3.69 mmol), cesium carbonate (1.68 g, 5.17 mmol), tris(dibenzylideneacetone-dipaladium(0) (101 mg, 0.11 mmol) and (S)-(2,2'-bis(di-p-tolylphosphino-l,l'-binaphthyl (98%, (5)-tol-BINAP) (113 mg, 0.17 mmol) (Ligand/Pd = 1.5) in anhydrous toluene (32 mL) using the procedure described in Example 2, step C. This procedure yielded an yellow solid, 1.31 g (3.24 mmol, 73%) of the desired product, mp 115-117°C. <br><br> MS: 405 (M+) <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -65- <br><br> Analysis for C24H2404N2-0.25 H2O: Calcd: C, 71.27; H, 5.98; N, 6.93. <br><br> Found: C, 70.48; H, 6.03; N, 6.85. <br><br> Preparation of 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid <br><br> The title compound was prepared 2-{4-[2-(3,4-dimethyl-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid methyl ester (1.12 g, 2.76 mmol), IN NaOH (50 mL) in EtOH (50 mL) and THF (50 mL) using the procedure described in Example 2. This procedure yielded a yellow solid, 1.03 g (2.63 mmol, 81%) of the desired product, mp 214-216°C. <br><br> Analysis for C23H2204N2-0.25 H20: Calcd: C, 69.99; H, 5.74; N, 7.18. <br><br> Found: C, 69.90; H, 5.82; N, 6.81. <br><br> EXAMPLE 17 <br><br> Preparation of 2-[[4-[2-(4-Chloro-3-trifluromethylphenyl)ethyl]phenyl]amino-benzoic acid <br><br> Step A (Scheme 1): Preparation of trans-1 -Chloro-2-trifluoromethyl-4-[2-(4-nitrophenyl)ethenyl]benzene <br><br> A mixture of p-nitrophenylacetic acid (51.85 g, 0.29 mol) and 4-chloro-3-trifluoromethylbenzaldehyde (47.85 g, 0.23 mol) in piperidine (19.5 g, 0.23 mol) was heated under N2 atmosphere to 150°C tol60°°C for 1 hour. The reaction mixture was cooled to 80°C to 100ooC and refluxing i-PrOH (150 mL) was added. The mixture was continued to cool to room temperature and then placed under refrigeration for 5 hours. The crystalline precipitate was filtered off, rinsed with cold /-PrOH, and dried at room temperature in a vacuum oven overnight to yield trans-1 -chloro-2-trifluoromethyl-4- [2-(4-nitrophenyl)ethenyl]benzene as an orange solid, 22.53 g (68.75 mmol, 30%). mp 173-174°C. <br><br> MS: 327.0 (M+) <br><br> Step B (Scheme 1): Preparation of 4-[2-(4-ChIoro-3-trifluoromethylphenyl)ethyl]-benzenamine <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -66- <br><br> The title compound was prepared from trans-1 -chloro-2-trifluoromethyl-4-[2-(4-nitrophenyl)ethenyl]benzene (22.53 g, 0.069 mol) and Ra-Ni (22 g) in THF (0.5 L) at 18°C to 29°C (AP = 20.5 psi) under a hydrogen atmosphere using the procedure described in Example 1, Step B. This procedure yielded a white solid, 5 20.0 g (66.73 mmol, 97%) of the desired product, mp 62-64°C. <br><br> MS: 298.1 (M+) <br><br> Preparation of 2-[[4-[2-(4-Chloro-3-trifluromethylphenyl)ethyl]phenyl]-aminobenzoic acid <br><br> To a cold solution of 4-[2-(4-chloro-3-trifluoromethylphenyl)ethyl]-10 benzenamine (4.33 g, 14.45 mmol) in THF (50 mL) at -78°C, was added LHMDS (43.35 mL, 43.35 mmol) (1M/THF) dropwise. Allowed the reaction mixture to stir for 10 minutes at -78°C. A solution of 2-fluorobenzoic acid (2.02 g, 14.45 mmol) in THF (50 mL) was added dropwise. The mixture was stirred for 2 hours at -78°C, then warmed to room temperature and let stir for additional 3 hours. The 15 reaction mixture was concentrated in vacuo (40°C) to remove the organic solvent. <br><br> This residue was acidified to pH 3 with 3N HCl (aq.). This precipitate was collected by filtration, rinsed with 10% HCl (40 mL), and dried in vacuum for overnight to give as a pale solid , 4.3 g (10.24 mmol, 70%) of the desired product mp 150-152°C. <br><br> 20 Analysis for C22Hi702N1ClF3-0.59 H20: Calcd: C, 61.39; H, 4.26; N, 3.25. Found: C, 61.01; H, 4.34; N, 3.30. <br><br> EXAMPLE 18 <br><br> Preparation of 2-[4-(3,4-Dichlorophenyl)phenylamino]benzoic acid <br><br> Preparation of o-Bromobenzoic acid potassium salt 25 To a solution of o-bromobenzoic acid (201.03 g, 1.0 mol) in MeOH <br><br> (500 mL), K2C03 (69 g, 1.0 mol) was added. The mixture was concentrated to give the desired product (239.1 g, 1.0 mol, 100%). <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -67- <br><br> Preparation of 2-[(4-Iodophenyl)amino] benzoic acid <br><br> A mixture of o-bromobenzoic acid potassium salt (47.8 g, 0.2 mol), 4-iodoaniline (43.8 g, 0.2 mol), K2CO3 (13.8 g, 0.1 mol), and cupric acetate (2.87 g, 6%) in diglyme (100 mL) was heated to reflux for 30 minutes. The reaction mixture was diluted with H2O (1.0 L) and filtered. The filtrate was acidified with diluted AcOH. The resulting precipitate was collected by filtration, washed with H2O and dried in a vacuum at 50°C for 16 hours. Recrystallization from EtOAc gave the desired product, a solid (29.7 g, 0.087 mol, 44%). mp 205-206°C. <br><br> Analysis for C^H^N^I: Calcd: C,45.05; H, 2.97; N, 4.13. Found: C, 45.05; H, 2.97; N, 3.92. <br><br> Preparation of 2-[4-(3,4-Dichlorophenyl)phenylamino]benzoic acid <br><br> A mixture of 3,4-dichlorophenylboronic acid (880 mg, 2.3 mmol), 2-[(4-iodophenyl)amino]benzoic acid (339 mg, 1 mmol), PdCl2"dppfCH2Cl2 [1,1'-bis(diphenylphosphino)ferrocene palladium (II) chloride, complexed with dichloromethane (1:1)] (67 mg, 0.082 mmol), K2CO3 (829 mg, 6 mmol), and H2O (2 mL) in dioxane (15 mL) was heated to reflux for 1 hour. The reaction mixture was diluted with EtOAc and filtered. The filtrate was treated with IN HCl, washed with H2O, brine, dried (Na2S04), and concentrated in vacuum to give a yellow solid. Purification by flash chromatography (silica gel, 10% MeOH/CH2Cl2) yielded 272 mg (0.76 mmol, 76%) of the desired product, mp &gt;220°C. <br><br> Analysis for Ci9Hi302NiCl2: Calcd: C, 63.23; H, 3.71; N, 3.88. <br><br> Found: C, 62.95; H, 3.73; N, 3.63. <br><br> By following the general procedures described above, the following additional invention compounds were prepared: <br><br> WO 00/76489 PCT/US00/1S071 <br><br> -68-EXAMPLE 19 <br><br> 2-{4-[3-(4-Diethylaminophenyl)propyl]phenylamino}benzoic acid MS: 403 (M+). <br><br> Analysis for C26H30^202"0-40 mol H2O: Calcd: C, 69.31; H, 6.87; N, 6.12. 5 Found: C, 69.29; H, 7.04; N, 6.35. <br><br> EXAMPLE 20 <br><br> 2-{4-[3-(4-Nitrophenyl)propyl]phenylamino}benzoic acid, mp 150-153°C. MS: 376 (M4). <br><br> EXAMPLE 21 <br><br> 10 2-{4-[3-(3-Nitrophenyl)propyl]phenylamino}benzoic acid, mp 164-167°C. <br><br> MS: 376 (M+). <br><br> Analysis for C22H20N2O4"2-20 mol H2O: Calcd: C, 63.51; H, 5.91; N, 6.73. <br><br> Found: C, 63.56; H, 5.45; N, 6.46. <br><br> EXAMPLE 22 <br><br> 15 2-{4-[3-(4-Aminophenyl)propyI]phenylamino}benzoic acid, mp 110-112°C. <br><br> MS: 347 (M+1+). <br><br> EXAMPLE 23 <br><br> 2-{4-[3-(3-Aminophenyl)propyl]phenylamino}benzoic acid, mp 109°C. MS: 333 (M+1+). <br><br> 20 EXAMPLE 24 <br><br> 2-{4-[2-(4-Aminophenyl)phenylamino}benzoic acid, mp 198-201°C. <br><br> MS: 333 (M+1+). <br><br> Analysis for C2iH20N2O2'®-l m°l H2O: Calcd: C, 75.47; H, 6.09; N, 8.38. <br><br> Found: C, 75.32; H, 6.12; N, 8.27. Found: C, 75.32; H 6.12; N, 8.27. <br><br> WO 00/76489 PCT/US00/15071 <br><br> -69-EXAMPLE 25 <br><br> 2-{4-[2-(4-Dipropylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride. mp 176-177°C <br><br> MS: 417 (M+I+). <br><br> Analysis for C27H32N2O2: Calcd: C, 71.59; H, 7.34; N, 6.18; CI, 7.83. Found: C, 71.31; H, 7.24; N, 6.19; CI, 7.74. <br><br> EXAMPLE 26 <br><br> 2-{4-[2-(4-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride monohydrate MS: 389 (M+1+). <br><br> Analysis for C25H28N202-HC1-H20: Calcd: C, 67.78; H, 7.05; N, 6.32; CI, 8.00. Found: C, 67.83; H, 7.01; N, 6.30; CI, 7.75. <br><br> EXAMPLE 27 <br><br> 2-{4-[3-(3-Dipropylaminophenyl)propyl]phenylamino}benzoic acid MS: 431 (M+1+). <br><br> Analysis for C28H34N202-0.2 H20: Calcd: C, 77.46; H, 7.99; N, 6.45. <br><br> Found: C, 77.43; H, 7.86; N, 6.40. <br><br> EXAMPLE 28 <br><br> 2- {4-[3-(3 -Dimethylaminophenyl)propyl]phenylamino} benzoic acid. <br><br> mp 115-117°C. <br><br> MS: 374 (M+), 375 (M+1+). <br><br> Analysis for C24H26N2C&gt;2-0.1 H2O: Calcd: C, 76.61; H, 7.02; N, 7.44. Found: C, 76.57; H, 7.21; N, 7.47. <br><br> EXAMPLE 29 <br><br> 2-{4-[3-(4-EthyIaminophenyl)propyl]phenylamino}benzoic acid, mp 133°C. MS: 375 (M+1+). <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -70- <br><br> Analysis for 02/^2^2^2'^^ H2O: Calcd: C, 76.61; H, 7.02; N, 7.44. Found: C, 76.62; H, 7.06; N, 7.36. <br><br> EXAMPLE 30 <br><br> 2-(N-{4-[3-(4-Diethylaminophenyl)propyl]phenyl}-N-ethyIamino)benzoic acid MS: 431 (M+1+). <br><br> Analysis for C28H34N2O2: Calcd: C, 78.10; H, 7.96; N, 6.51. Found: C, 78.02; H, 8.17; N, 6.50. <br><br> EXAMPLE 31 <br><br> 2-{4-[2-(3-Dibenzylaminophenyl)ethyl]phenylamino}benzoic acid, mp 95.5-97.5°C. <br><br> Analysis for C35H32N2O2: Calcd: C, 82.00; H, 6.29; N, 5.46. Found: C, 81.81; H, 6.58; N, 5.44. <br><br> EXAMPLE 32 <br><br> 2- {4-[3 -(3-Diethylaminophenyl)propyl]phenyIamino } benzoic acid MS: 403 (M+l+). <br><br> Analysis for C26H3oN202"0.1 H20: Calcd: C, 77.23; H, 7.53;N, 6.93. Found: C, 77.14; H, 7.82; N, 6.88. <br><br> EXAMPLE 33 <br><br> 2-{4-[2-(3-Aminophenyl)ethyl]phenylamino}benzoic acid, mp 182-184°C. MS: 333 (M+1+). <br><br> Analysis for C2iH2()N202-0.25 H20: Calcd: C, 74.87; H, 6.13; N, 8.43. <br><br> Found: C, 74.86; H, 6.16; N, 8.32. <br><br> EXAMPLE 34 <br><br> 2-{4-[3-(4-Dimethylaminophenyl)propyl]phenylamino}benzoic acid MS: 375 (M+1+). <br><br> Analysis for C24H26N202-0.1 H20: Calcd: C, 76.61; H, 7.02; N, 7.44. Found: C, 76.52; H, 7.22; N, 7.49. <br><br> WO 00/76489 PCT/Us00/I5071 <br><br> -71-EXAMPLE 35 <br><br> 2-{4-[2-(4-AcetyIaminophenyl)ethyl]phenylamino} benzoic acid, mp 224°C. MS: 375 (M+l+). <br><br> EXAMPLE 36 <br><br> 2-{4-[2-(3-Acetylaminophenyl)ethyl]phenylamino}benzoic acid, mp 213-215°C. MS: 375 (M+l+). <br><br> EXAMPLE 37 <br><br> 2- {4-[2-(3 -Dipropylaminophenyl)ethyl]phenylamino} benzoic acid monohydrochloride. mp 189-193°C. <br><br> MS: 417 (M+l+). <br><br> Analysis for C27H32N202-HC1: Calcd: C, 71.58; H, 7.34; N, 6.18; CI, 7.83. <br><br> Found: C, 71.48; H, 7.35; N, 6.10; CI, 7.66. <br><br> EXAMPLE 38 <br><br> 2-{4-[2-(3-Dibutyiaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride. mp 175-180°C. <br><br> MS: 445 (M+). <br><br> Analysis for C29H36N202-HC1: Calcd: C, 72.40; H, 7.75; N, 5.82; CI, 7.37. <br><br> Found: C, 72.61; H, 7.95; N, 5.78; CI, 7.23. <br><br> EXAMPLE 39 <br><br> 2-{4-[3-(4-Acetylaminophenyl)propyl]phenylamino}benzoic acid, mp 176-178°C. MS: 389 (M+l+). <br><br> EXAMPLE 40 <br><br> 2-{4-[3-(3-Acetylaminophenyl)propyl]phenylamino}benzoic acid, mp 140-145°C. MS: 389 (M+1+). <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -72- <br><br> EXAMPLE 41 <br><br> 2-{4-[2-(3-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride. mp 166-171°C. <br><br> MS: 389 (M+l+). <br><br> Analysis for C25H28N202-HC1: Calcd: C, 70.66; H, 6.88; N, 6.59; CI, 8.34. Found: C, 70.48; H, 6.89; N, 6.57; CI, 18.39. <br><br> EXAMPLE 42 <br><br> 2-{4-[2-(3-Piperidin-l-ylphenyl)ethyl]phenylamino}benzoic acid monohydrochloride. mp 187-193°C. <br><br> MS: 401 (M+1+). <br><br> Analysis for C26H28N202-HC1: Calcd: C, 71.46; H, 6.69; N, 6.41; CI, 8.11. Found: C, 71.28; H, 6.73; N, 6.35; CI, 8.30. <br><br> EXAMPLE 43 <br><br> 2-{4-[3-(4-Dipropylaminophenyl)propyl]phenylamino}benzoic acid MS: 431 (M+1+). <br><br> Analysis for C28H34N2O2: Calcd: C, 78.10; H, 7.96; N, 6.51. Found: C, 77.91; H, 8.03; N, 6.43. <br><br> EXAMPLE 44 <br><br> 2-{4-[3-(4-Dibutylaminophenyl)propyl]phenylamino}benzoic acid MS: 459 (M+l+). <br><br> Analysis for C30H38N2O2: Calcd: C, 78.56; H, 8.35; N, 6.11. Found: C, 78.40; H, 8.50; N, 6.19. <br><br> EXAMPLE 45 <br><br> 2- {4-[3 -(3 -Dibutylaminophenyl)propyl]phenylamino } benzoic acid MS: 459 (M+l+). <br><br> Analysis for C30H38N2O2: Calcd: C, 78.56; H, 8.35; N, 6.11. Found: C, 78.40; H, 8.43; N, 6.11. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -73-EXAMPLE 46 <br><br> 2-(4-{3-[4-(lH-Pyrrol-l-yl)phenyl]propyl}phenylamino)benzoic acid, mp 13I-136°C. <br><br> MS: 397 (M+1+). <br><br> Analysis for C26H24N2C&gt;2"0.2 H20: Calcd: C, 78.05; H, 6.15; N, 7.00. Found: C, 77.95; H, 6.17; N, 7.08. <br><br> EXAMPLE 47 <br><br> 2-{4-[3-(4-Piperidin-l-ylphenyl)propyl]phenylamino}benzoic acid MS: 415 (M+l+). <br><br> Analysis for C27H3oN202-0.2 H20: Calcd: C, 77.55; H, 7.33; N, 6.70. Found: C, 77.37; H, 7.35; N, 6.63. <br><br> EXAMPLE 48 <br><br> 2-{4-[3-(4-Diethylcarbamoylphenyl)propyl]phenylamino}benzoic acid, mp 57-62°C. <br><br> MS: 431 (M+l4). <br><br> Analysis for C27H30N2O3-O.3 H2O: Calcd: C, 74.39; H, 7.07; N, 6.43. Found: C, 74.23; H, 6.97; N, 6.27. <br><br> EXAMPLE 49 <br><br> 2-{4-[3-(4-Carboxyphenyl)propyl]phenylamino}benzoic acid, mp 236-239°C. MS: 375 (M+). <br><br> EXAMPLE 50 <br><br> 2-{4-[3-(4-Diethylaminomethylphenyl)propyl]phenylamino}benzoic acid, mp 137°C. <br><br> MS: 417 (M+l+). <br><br> EXAMPLE 51 <br><br> 2- {4-[3 -(4-Propylaminophenyl)propyl]phenylamino} benzoic acid MS: 389 (M+l+). <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -74- <br><br> Analysis for C25H28N202-0.2 H20: Calcd: C, 76.58; H, 7.30; N, 7.14. Found: C, 76.61; H, 7.29; N, 7.03. <br><br> EXAMPLE 52 <br><br> 2-{4-[3-(3-Propylaminophenyl)propyl]phenylamino}benzoic acid MS: 389 (M+1+). <br><br> Analysis for C25H28N2O2O.I H20: Calcd: C, 76.93; H, 7.28; N, 7.18. Found: C, 76.85; H, 7.44; N, 7.06. <br><br> EXAMPLE 53 <br><br> 2- {4- [3-(4-Pyrrolidin-1 -yl-phenyl)-propyl]-phenylamino } -benzoic acid, mp 171-177°C. <br><br> MS: 401 (M+1+). <br><br> Analysis for C26H28N202-0.2 H20: Calcd: C, 77.27; H, 7.08; N, 6.93. Found: C, 77.09; H, 6.97; N, 6.96. <br><br> EXAMPLE 54 <br><br> 2-(4-[3-(3-Piperidin-1 yl-phenyl)-propyl]-phenylamino}-benzoic acid, mp 59-61°C. <br><br> MS: 415 (M+1+). <br><br> Analysis for C27H3qN202-0.3 H20: Calcd: C, 77.22; H, 7.34; N, 6.67. Found: C, 77.18; H, 7.25; N, 6.49. <br><br> EXAMPLE 55 <br><br> {5 - [(1 -Butyl-1,2,3,4-tetrahydro-6-quinolyl)methylidene]-4-oxo-2-thioxothiazolidin-3-yl}acetic acid, mp 222-224°C. <br><br> MS: 391 (M+1+). <br><br> EXAMPLE 56 <br><br> {5-[(l-Butyl-2,3-dihydro-lH-indol-5-yl)methylidene]-4-oxo-2-thioxothiazolidin- <br><br> 3-yl}acetic acid, mp &gt;250°C. <br><br> MS: 377 (M+l+). <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -75- <br><br> Analysis for C] 8H20N203S2-0.4 H2O: Calcd: C, 56.34; H, 5.46; N, 7.30; S, 16.71. Found: C, 56.27; H, 5.18; N, 7.31; S, 16.74. <br><br> EXAMPLE 57 <br><br> 3-{5-[( 1-Butyl-1,2,3,4-tetr ahydroquinolin-6-yl)methylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}propanoic acid, mp 214-215°C. <br><br> MS: 405 (M+1+). <br><br> EXAMPLE 58 <br><br> 4- { 5- [(1 -Butyl-1,2,3,4-tetrahydroquinolin-6-yl)methylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}butanoic acid, mp 152-154°C. <br><br> MS: 417 (M"l+), 418 (M+), 419 (M+l+). <br><br> Analysis for C21H26N2O3S2 O.2 H2O: Calcd: C, 59.74; H, 6.30; N, 6.64; S, 15.19. Found: C, 59.59; H, 6.16; N, 6.52; S, 15.38. <br><br> EXAMPLE 59 <br><br> 2- {4- [3-(3,4-Dichloro-phenyl)-propyl]phenylamino } -5 -methyl-benzoic acid, mp 98-99°C. <br><br> MS: 414 (M+). <br><br> EXAMPLE 60 <br><br> N-(2-{4-[3-(3,4-Dichloro-phenyl)-propyI]-phenylamino}-benzoyl)-methanesulfonamide was prepared by reacting the product from Example 9 with methanesulfonamide. mp 53-61°C. <br><br> Analysis for C23H22Cl2N2O3S-0.13 H20: Calcd: C, 57.58; H, 4.68; N, 5.84. Found: C, 57.20; H, 4.66; N, 5.51. <br><br> EXAMPLE 61 <br><br> 2- {4-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino }-5-nitro-benzoic acid. mp214-216°C. <br><br> Analysis for C23^2^04-0.25 H20: Calcd: C, 69.99; H, 5.74; N, 7.18. <br><br> Found: C, 69.90; H, 5.82; N, 6.81. <br><br> WO 00/76489 PCT/US00/15071 <br><br> -76-EXAMPLE 62 <br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid, mp 239-244°C. MS: 439 (MH+). <br><br> EXAMPLE 63 <br><br> 2- {4- [2-(4-ChIoro-3 -trifluoromethyl-phenyl)-ethyl]-phenyl amino } -5-nitro-benzoic acid, mp 207-209°C. <br><br> Analysis for C22H16CIF3N2O4: Calcd: C, 56.85; H, 3.47; N, 6.03. <br><br> Found: C, 56.75; H, 3.71; N, 5.83. <br><br> EXAMPLE 64 <br><br> 5-Amino-2-{4-[2-(3,4-Dichloro-phenyI)-ethyl]-phenylamino}-benzoic acid was prepared by reacting the product from Example 2 with hydrogen gas in the presence of Raney nickel, mp 137-142°C. <br><br> Analysis for C2iH18Cl2N2020.96 mol THF: Calcd: C, 63.94; H, 4.72; N, 6.00. Found: C, 64.33; H, 4.91; N, 6.35. <br><br> EXAMPLE 65 <br><br> 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid, mp 198-202°C. <br><br> Analysis for C2iH18N2O4-0.11 H20: Calcd: C, 69.22; H, 5.04; N, 7.69. <br><br> Found: C, 69.59; H, 5.27; N, 7.22. <br><br> EXAMPLE 66 <br><br> 2-{4-[2-(4-Fluoro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid, mp 148-150°C. <br><br> Analysis for C22H17F4NO2: Calcd: C, 65.51; H, 4.25; N, 3.47. Found: C, 65.51; H, 4.13; N, 3.46. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -77-EXAMPLE 67 <br><br> 2-{4-[2-(3s4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid mp 203-208°C. <br><br> Analysis for C21H16F2N2O4: Calcd: C, 63.32; H, 4.05; N, 7.03. <br><br> Found: C, 62.94; H, 4.37; N, 6.87. <br><br> EXAMPLE 68 <br><br> {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenyl} -[2-( 1 H-tetrazol-5 -yl)-phenyl] -amine was prepared as described in Example 1, using a tetrazole fluoro intermediate that was synthesized from commercially available 2-fluorobenzonitrile and sodium azide under standard reaction conditions, mp 129 shrink, 152-157°C. <br><br> Analysis for C2iHi7Cl2N5'0.15 EtOAc-O.15 Hexane: Calcd: C, 61.80; H, 4.64; N, 16.12. Found: C, 61.61; H, 4.28; N, 15.83. <br><br> EXAMPLE 69 <br><br> 2- {4-[2-(4-Fluoro-3 -trifluoromethyl-phenyl)-ethyl]-phenylamino} -5-nitro-benzoic acid, mp 190-193°C. <br><br> Analysis for C22H16F4N2O4: Calcd: C, 58.93; H, 3.60; N, 6.25. <br><br> Found: C, 58.69; H, 3.42; N, 6.57. <br><br> EXAMPLE 70 2-(4-Phenethyl-phenylamino)-benzoic acid, mp 173-182°C. <br><br> Analysis for C2iH19N02: Calcd: C, 79.47; H, 6.03; N, 4.41. Found: C, 79.42; H, 5.97; N, 4.47. Found: C, 79.59; H, 6.03; N, 4.50. <br><br> EXAMPLE 71 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-fluoro-benzoic acid, mp 180-182°C. <br><br> Analysis for C2iH]gCl2FN02-0.06 H2O: Calcd: C, 62.23; H, 4.01; N, 3.46. Found: C, 61.83; H, 4.04; N, 3.29. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -78-EXAMPLE 72 <br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -nicotinic acid. <br><br> mp 168-171°C. <br><br> Analysis for C2qH15CI2N2O2: Calcd: C, 62.03; H, 4.16; N, 7.23. <br><br> Found: C, 62.11; H, 4.17; N, 7.07. <br><br> EXAMPLE 73 <br><br> 2-{4-[2-(3-Chloro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid, mp 192.5-194.5°C. <br><br> Analysis for C21H17CIN2O4: Calcd: C, 63.56; H, 4.32; N, 7.06. Found: C, 63.83; H, 4.62; N, 6.79. <br><br> EXAMPLE 74 <br><br> 2- {4-[2-(4-Chloro-phenyl)-ethyl]-phenylamino} -5-nitro-benzoic acid, mp 210-212°C. <br><br> Analysis for C2lH17CIN2O4-0.26 H20: Calcd: C, 62.82; H, 4.40; N, 6.98. Found: C, 62.51; H, 4.34; N, 6.58. <br><br> EXAMPLE 75 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic acid, mp 153-160°C. <br><br> Analysis for C99HiqC1?NC&gt;2-0.61 H2O: Calcd: C, 64.25; H, 4.96; N, 3.41. Found: C, 63.87; H, 4.64; N, 3.55. <br><br> EXAMPLE 76 <br><br> 2- {4-[2-(2-Chloro-phenyl)-ethyl]-phenylamino } -5-nitro-benzoic acid, mp 236-238°C. <br><br> EXAMPLE 77 <br><br> 2-{4-[2-(2,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid, mp 200.5-202.5°C. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -79- <br><br> Analysis for C2iH16Cl2N204: Calcd: C, 58.49; H, 3.74; N, 6.50. <br><br> Found: C, 58.33; H, 3.67; N, 6.29. <br><br> EXAMPLE 78 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-trifluoromethyl-benzoic acid, mp 130-132°C. <br><br> Analysis for C22Hi6Cl2F3N02: Calcd: C, 58.17; H, 3.55; N, 3.08. <br><br> Found: C, 58.25; H, 3.65; N, 3.05. <br><br> EXAMPLE 79 <br><br> 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid, mp &gt;260°C. <br><br> EXAMPLE 80 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]-phenyIamino}-5-dimethylamino-benzoic acid, mp 75-80°C. <br><br> EXAMPLE 81 <br><br> 2-{4-[2-(3,5-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid, mp 191-194°C. Analysis for C2iHi7Cl2N02: Calcd: C, 65.30; H, 4.44; N, 3.63. Found: C, 65.38; H, 4.29; N, 3.52. <br><br> EXAMPLE 82 <br><br> 2-(4-{2-[(4aS,8aR)-4-(Octahydro-isoquinolin-2-yl)-phenyl]-ethyl}-phenylamino)-benzoic acid was prepared according to Example 1 using a decahydroisoquinoline aldehyde which was prepared from trans-decahydroisoquinoline and para-fluorobenzaldehyde under standard reaction conditions, mp 203-206°C. <br><br> Analysis for C3oH34N202-0.12 H20: Calcd: C, 78.89; H, 7.56; N, 6.13. <br><br> Found: C, 78.49; H, 7.58; N, 5.90. <br><br> The following examples are prepared according to the foregoing methods, or by utilizing standard combinatorial synthetic methodology by reacting halo substituted benzoate esters with a substituted aniline to form the corresponding <br><br> wo 00/76489 <br><br> PCT/US00/15071 <br><br> -80- <br><br> diarylamine, followed by saponification to the benzoic acid of Formula I. The reactions are carried out on 0.15 mmol scale as follows. Solutions of each halo benzoate reactant (0.18 M) in toluene are placed in 2 dram reaction vials. Each aniline reactant is dissolved in anhydrous toluene to give 0.15 M solutions. A Distriman pipet is used to add 1 mL (0.15 mmol, 1 eq) of each halo benzoate solution to the appropriate vials containing 1 mL (0.18 mmol, 1.2 eq) of the aniline reactants. A catalyst solution is prepared by dissolving 0.025 M of <br><br> Pd2(dba)3 (dipalladium-tridibenzylidene acetone) and 0.075 M of BINAP (2,2 -bis(diphenylphosphino)-l,l'-binapthyl) in toluene, and 0.25 mL of the catalyst solution is added to each reaction vial. A base, generally cesium carbonate (68 mg, 0.21 mmol, 1.40 eq) is added to each reaction vial, and the vials are capped and placed in a shaker oven and heated at 100°C for 48 hours. The reaction mixtures are then cooled, and the reaction solvents are removed by evaporation. The solid residue is suspended in 400 [J.L of ethyl acetate and filtered to remove all catalyst. The filtrates are concentrated to dryness by evaporation to provide compounds of Formula I, wherein the benzoic acid portion is esterified (e.g., benzyl or methyl ester). The esters are dissolved in 500 jiL of THF/ethanol (1:1 v/v) to which is added 300 jxL of 5 M sodium hydroxide. The solutions are shaken for 5 hours at 60°C and then cooled and concentrated to dryness by evaporation of the solvents to provide the desired compounds of Formula I. Typical compounds prepared by this method are as follows. The structure of the compounds are generally confirmed by mass spectral analysis. <br><br> EXAMPLE 83 <br><br> 2-(3',5'-Dichloro-3-methyl-biphenyl-4-ylamino)-benzoic acid MS: 371; MW: 372.2495. <br><br> EXAMPLE 84 <br><br> 2-(3',5'-Dibromo-3-methyl-biphenyl-4-ylamino)-benzoic acid MS: 459; MW: 461.1515. <br><br> WO 00/76489 PCT/US00/15071 <br><br> -81-EXAMPLE 85 <br><br> 2-(4- l,3-Benzodioxol-5-yl-2-methyl-phenylamino)-benzoic acid MS: 347; MW: 347.3683. <br><br> EXAMPLE 86 2-(2,2',4'-Trichloro-biphenyl-4-ylamino)-benzoic acid MS: 391; MW: 392.6678. <br><br> EXAMPLE 87 <br><br> 2-(2-Chloro-3 ',4'-difluoro-biphenyl-4-ylamino)-benzoic acid MS: 359; MW: 359.7578. <br><br> EXAMPLE 88 2-(3 '-Bromo-2-chloro-biphenyl-4-ylamino)-benzoic acid MS: 401; MW: 402.6737. <br><br> EXAMPLE 89 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]-phenylamino}-5-nitro-benzoic acid <br><br> EXAMPLE 90 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-nitro-benzoic acid <br><br> EXAMPLE 91 <br><br> 3-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 92 <br><br> 5-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid <br><br> EXAMPLE 93 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 94 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4,5-dimethoxy-benzoic acid <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -82-EXAMPLE 95 <br><br> 2-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-3-nitro-benzoic acid <br><br> EXAMPLE 96 <br><br> 3-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 97 <br><br> 5-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-isophthalic acid <br><br> EXAMPLE 98 <br><br> 2-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 99 <br><br> 4-(4-{2-[(4aS,8aR)-4-(Octahydro-isoquinolin-2-yl)-phenyl]-ethyl}-phenylamino)-benzoic acid <br><br> EXAMPLE 100 <br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-5-methoxy-benzoic acid <br><br> EXAMPLE 101 <br><br> 2- {4-[2-(3-Methoxy-phenyl)-ethyl]-phenylamino } -benzoic acid <br><br> EXAMPLE 102 2- {4-[2-(3 -Bromo-phenyl)-ethyl]-phenylamino} -benzoic acid <br><br> EXAMPLE 103 2-{4-[2-(3-Fluoro-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 104 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid <br><br> EXAMPLE 105 <br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-nicotinic acid <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -83-EXAMPLE 106 <br><br> 2-[2-(4-Fluoro-3-trifluoromethyl-phenyl)-2,3-dihydro-lH-isoindoI-5-ylamino]-benzoic acid <br><br> EXAMPLE 107 <br><br> 2-{4-[2-(3-Fluoro-4-methyl-phenyl)-ethyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 108 <br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylammo}-5-nitro-benzoic acid <br><br> EXAMPLE 109 <br><br> 4-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-benzoic acid <br><br> EXAMPLE 110 <br><br> 4- {4-[3 -(4-Diethylamino-phenyl)-propyl]-phenylamino } -3 -methoxy-6-nitro-benzoic acid <br><br> EXAMPLE 111 <br><br> 4- {4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino} -3 -methoxy-benzoic acid <br><br> EXAMPLE 112 <br><br> 2-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid <br><br> EXAMPLE 113 <br><br> {4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenyl}-(2-methoxy-5-nitro-phenyl)-amine <br><br> EXAMPLE 114 <br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-3-nitro-benzoic acid <br><br> EXAMPLE 115 <br><br> 3-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-benzoic acid <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -84-EXAMPLE 116 <br><br> 2-{4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 159-161°C. <br><br> EXAMPLE 117 <br><br> 5 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid monosodium; mp 107-108°C. <br><br> EXAMPLE 118 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid monopotassium; mp &gt;200°C. <br><br> 10 EXAMPLE 119 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid calcium salt (1:1); mp &gt;220°C. <br><br> EXAMPLE 120 <br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -benzoate-2-hy droxy- 1,1-bis-15 hydroxymethyl-ethyl-ammonium; mp 185-187°C. <br><br> EXAMPLE 121 <br><br> 2-{4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamino}-5-methoxy-benzoic acid; mp 155-158°C. <br><br> EXAMPLE 122 <br><br> 20 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 184-185°C. <br><br> EXAMPLE 123 <br><br> 2-{3-[2-(4-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 155-157°C. <br><br> EXAMPLE 124 <br><br> 2-{3-[2-(3,4-Dimethyl-phenyl)-ethyI]-phenylamino}-benzoic acid; mp 182-25 184°C. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -85-EXAMPLE 125 <br><br> 2-{4-[2-(2,4-Dimethoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 180-181°C. <br><br> EXAMPLE 126 <br><br> 2-{4-[2-(2-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 140-143°C. <br><br> EXAMPLE 127 <br><br> 2-{4-[2-(2-Hydroxy-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 218-219°C. <br><br> EXAMPLE 128 <br><br> 2-{4-[2-(3-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 152-154°C. <br><br> EXAMPLE 129 <br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-benzoic acid; mp 200-202°C. <br><br> EXAMPLE 130 <br><br> 2-{4-[2-(2,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 181-183°C. <br><br> EXAMPLE 131 <br><br> 3-{4-[2-(3,4-Dicliloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 137-138°C. <br><br> EXAMPLE 132 <br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 214-215°C. <br><br> EXAMPLE 133 <br><br> 2-{4-[2-(3,4,5-Trimethoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 146-147°C. <br><br> EXAMPLE 134 <br><br> 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; mp 153-154°C. <br><br> WO 00/76489 PCT/USO0/15071 <br><br> -86-EXAMPLE 135 <br><br> 2-{4-[5-(3,4-Dichloro-phenyl)-pentyl]-phenylamino}-benzoic acid; mp 106-108°C. <br><br> EXAMPLE 136 <br><br> 5 2- {4- [2-(4- { 2-Hydroxycarbonylphenylamino}phenyl)ethyl]-phenylamino} - <br><br> benzoic acid; MS 451 (M-*). <br><br> EXAMPLE 137 <br><br> 2-(3',5'-Dichloro-biphenyl-4-ylamino)-benzoic acid; mp &gt;220°C. <br><br> EXAMPLE 138 <br><br> 10 4-{4-[3-(3,4-Dichloro-phenyl)-propyl]-phenyIamino}-2-methoxy-5-nitro-benzoic acid; mp 74-78°C. <br><br> EXAMPLE 139 <br><br> 2-{4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino}-5-fluoro-benzoic acid; mp 122-123°C. <br><br> 15 EXAMPLE 140 <br><br> 5-Amino-2- {4-[5-(3,4-dichloro-phenyl)-pentyl]-phenylamino} -benzoic acid; mp 182-184°C. <br><br> EXAMPLE 141 <br><br> N-(2-{4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino}-benzoyl)-C,C,C-20 trifluoro-methanesulfonamide; MS 531 (M"). <br><br> EXAMPLE 142 <br><br> N-(2- {4- [3 -(3,4-Dichloro-pheny l)-propyl]-phenylamino} -benzoyl)-benzenesulfonamide; MS 539. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -87-EXAMPLE 143 <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -5 -trifluoromethyl-benzoic acid; mp 190-192°C. MS 453 (M"1). <br><br> EXAMPLE 144 <br><br> 5 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid; mp 264-266°C. <br><br> EXAMPLE 145 <br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino} -4-trifluoromethyl-benzoic acid; mp 134-136°C; MS 454 (M+). <br><br> 10 EXAMPLE 146 <br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifluoromethyl-benzoic acid; MS 454 (M+). <br><br> EXAMPLE 147 <br><br> 2-({4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyl}-methyl-amino)-5-dimethylamino-15 benzoic acid; mp 128-131°C. <br><br> EXAMPLE 148 <br><br> 2-({4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyl} -methyl-amino)-benzoic acid; MS 400 (M+). <br><br> EXAMPLE 149 <br><br> 20 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-dipropylamino-benzoic acid; MS 485 (M+). <br><br> EXAMPLE 150 <br><br> 5-Dibutylamino-2-{4-[2-(3,4-dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; MS 513 (M+). <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -88-EXAMPLE 151 <br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -5-diethylamino-benzoic acid; mp 106-110°C. <br><br> EXAMPLE 152 <br><br> 5 2,2'-[l,2-Ethanediylbis (4,l-phenyleneimino)]bis-benzoic acid <br><br> EXAMPLE 153 <br><br> 4-[3-[4-(Diethylamino)phenyl]propyl]-N-(2-methoxy-5-nitrophenyl)-benzinamine <br><br> EXAMPLE 154 2-{3-[2-(4-Chlorophenyl)ethyl]phenylamino}-benzoic acid <br><br> 10 EXAMPLE 155 <br><br> 2-{3-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-benzoic acid <br><br> EXAMPLE 156 <br><br> 2-{3-[3-(4-Diethylaminophenyl)propyl]phenylamino}-benzoicacid <br><br> EXAMPLE 157 <br><br> 15 2-{3-[3-(4-Di-n-propylaminophenyl)propyl]phenylamino}-benzoic acid <br><br> The following Examples 158-163 illustrate the use of invention compounds as starting materials and intermediates in the synthesis of other invention compounds and derivatives. The examples illustrate reduction of nitro groups to amino groups, alkylation of amino group, and esterification of 20 carboxylic acid groups. These reactions are depicted in the following generalized Scheme 12. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -89- <br><br> Scheme 12 <br><br> I <br><br> h2n^,chA0-™^) <br><br> COOH reduction <br><br> COOH <br><br> alkylation \esterification <br><br> R' <br><br> Rb—K <br><br> COOH COOE <br><br> esterification \ / alkylation <br><br> R' <br><br> / <br><br> Rb-N^-,CH2)n^&gt;NH^ <br><br> COOE <br><br> | saponification <br><br> COOH <br><br> where and Rc are as defined above, and E is an ester forming group such as Cj-Cg alkyl (e.g., methyl, 2,2,2-trichloroethyl), benzyl, diphenylmethyl, or the like. <br><br> EXAMPLE 158 2-{4-[3-(4-Nitrophenyl)propyl]phenylamino}benzoic acid <br><br> To a slurry of 4-[3-(4-nitrophenyl)propyl]aniline (4.08 g, 15.9 mmol) and 2-bromobenzoic acid (3.52 g, 17.5 mmol) in i-PrOH (100 mL) was added <br><br> WO 00/76489 PCT/US00/15071 <br><br> -90- <br><br> Cu(OAc)2 (87 mg, 0.478 mmol) and KOAc (3.44 g, 35.0 mmol) at room temperature. The resulting mixture was allowed to heat under reflux for 23 hours, <br><br> then cooled to room temperature. After removing the solvent under reduced pressure, the residue was diluted with water (100 mL) and basified with aqueous 1.0 M-NaOH solution to pH 9.0. The aqueous layer was washed with Et20 (20 mL, twice) and acidified with aqueous 1.0 M-HC1 solution to pH 3.0. The precipitate formed was filtered by suction and dried at 60°C in vacuo, affording the title compound as a beige solid (5.75 g, 96% yield), mp 150-153°C. <br><br> MS (Fab): 376 (MH+). <br><br> EXAMPLE 159 2-{4-[3-(4-Aminophenyl)propyl]phenylamino}benzoic acid <br><br> To a solution of 2-{4-[3-(4-nitrophenyl)propyl]phenylamino}benzoic acid (Example 158) (3.0 g, 7.97 mmol) in DMF (40 mL) was added 10% Pd-C (300 mg) at room temperature under argon atmosphere. Hydrogen gas (1 atm) was introduced into the flask and the mixture was stirred for 14 hours at room temperature. The reaction mixture was filtered through a Celite pad to remove Pd-C and concentrated in vacuo. The residue was diluted with MeOH (ca. 50 mL) and concentrated in vacuo. This operation was repeated 3 times to remove any trace of DMF. The residue was diluted with MeOH again, and insoluble stuff was removed by filtration. Removing the solvent of the filtrate in vacuo afforded an oil, which was diluted with CH3CN (50 mL) and added dropwise water (100 mL) <br><br> slowly. The precipitate formed was filtered and dried at 60°C in vacuo, affording the title compound as a white solid (2.34 g, 85% yield), mp 110-112°C. <br><br> MS (Fab): 347 (MH+). <br><br> EXAMPLE 160 <br><br> 2-{4-[3-(4-Aminophenyl)propyl]phenylamino)benzoic acid methyl ester <br><br> To a solution of 2-{4-[3-(4-aminophenyl)propyl]phenylamino}benzoic acid (Example 159) (2.34 g, 6.75 mmol) in MeOH (50 mL) was added concentrated H2SO4 (1.0 mL) at room temperature. The mixture was stirred under reflux for 3.0 days. The reaction was quenched with Et3N (10 mL) at 5°C, and the <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -91- <br><br> solvent was removed under reduced pressure. The residue was diluted with water (20 mL) and extracted with Et20 (20 mL, 4 times). The combined ether layer was washed with water (10 mL) and brine (10 mL), and dried over anhydrous Na2SC&gt;4. The solvent was removed under reduced pressure and purification by column chromatography afforded crude title compound as a yellow amorphous material (2.59 g). This material was used without further purification. <br><br> EXAMPLE 161 <br><br> 2-{4-[3-(4-Diethylaminophenyl)propyl]phenylamino}benzoic acid methyl ester and 2-{4-[3-(4-Ethylaminophenyl)propyl]phenylamino}benzoic acid methyl ester <br><br> To a solution of the crude ester described above (2.59 g, ca. 6.75 mmol) and CH3CHO (2.0 mL, 35.1 mmol) in CH3CN (50 mL) was added NaBH3CN (1.70 g, 27.0 mmol) at 5°C, and the suspension was stirred for 30 minutes while the pH was monitored and aqueous 1.0 M-HCl solution was added to maintain the mixture moderately acidic (pH 3.0-4.0). The reaction mixture was allowed to warm up to room temperature over 1.0 hour and then basified with aqueous 1.0 M-NaOH solution to pH 9.0. The reaction mixture was concentrated under reduced pressure to remove CH3CN, and the resulting aqueous solution was acidified with aqueous 1.0 M-HCl solution to pH 3.0. The aqueous solution was extracted with CHCI3 (20 mL, 3 times), and the combined extract was washed with brine (5 mL). After drying over anhydrous Na2SC&gt;4, the solvent was removed under reduced pressure and purified by column chromatography (silica gel 60N, n-hexane/CHCl3/Et3N 50:98:2). First eluted was the dialkylated product as a yellow amorphous material (1.07 g, 38%). <br><br> MS (Fab): 417 (MH+). <br><br> Subsequently eluted was the monoalkylated product as a yellow amorphous material (0.79 g, 30%). <br><br> MS (Fab): 389 (MH+). <br><br> EXAMPLE 162 <br><br> 2- {4- [3-(4-Diethylaminophenyl)propyl]phenylamino} benzoic acid <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -92- <br><br> To an emulsion of 2-{4-[3-(4-diethylaminophenyl)propyl]phenylamino}-benzoic acid methyl ester (1.68 g, 4.03 mmol) in EtOH (50 mL) was added aqueous 3 M-KOH solution (4.0 mL, 12.0 mmol) at room temperature, then the mixture was allowed to heat under reflux for 40 minutes. The reaction mixture 5 was cooled to room temperature and neutralized with aqueous 1.0 M-HCl solution to pH 9.0. The mixture was concentrated under reduced pressure to remove EtOH, and the resulting aqueous solution was extracted with CHCI3 (50 mL, 3 times). The combined extract was washed with brine (10 mL) and dried over anhydrous Na2S04- The solvent was removed under reduced pressure and purification by 10 column chromatography (silica gel 60N, conc NH40H/Me0H/CHC 13 0.2:2:100 <br><br> to 0.5:5:100) afforded a yellow oil. This oil was diluted with acetone, and the solution was concentrated under reduced pressure at room temperature to give the title compound as an amorphous solid (1.62 g, 99% for 0.2 hydrate). <br><br> MS (Fab): 403 (MH+). <br><br> 15 Analysis for C26H30N202-0.20 H20: Calcd: C, 76.89; H, 7.54; N, 6.90. <br><br> Found: C, 76.73; H, 7.67; N, 7.10. <br><br> EXAMPLE 163 <br><br> 2-{4-[3-(4-Ethylaminophenyl)propyl]phenylamino}benzoic acid <br><br> The title compound was prepared from 2-{4-[3-(4-ethylaminophenyl)-20 propyl]phenylamino} benzoic acid methyl ester (from Example 161), EtOH (10 mL), and 3 M-KOH solution (1.0 mL) using the procedure described in Example 162. This procedure yielded a yellow solid, 253 mg of the desired product (90% for 0.1 hydrate). <br><br> MS (Fab): 375 (MH+). <br><br> 25 Analysis for C24H26N202-0.10 H20: Calcd: C, 76.61; H, 7.02; N, 7.44. <br><br> Found: C, 76.62; H, 7.06; N, 7.36. <br><br> WO 00/76489 <br><br> PCT/USOO/15071 <br><br> -93- <br><br> BIOLOGICAL EXAMPLES <br><br> Representative compounds of Formula I have been evaluated in several in vitro and in vivo assays which are well-established as indicative of clinical usefulness in treating Alzheimer's disease. <br><br> AMYLOID ASSAYS <br><br> BASSR (Beta-Amvloid Self-Seeding Radioassav) <br><br> An assay for inhibitors of self-seeded amyloid fibril growth <br><br> Materials: <br><br> Stock Solutions: <br><br> Assay Buffer - 50 mM sodium phosphate, pH 7.5, 100 mM NaCl, 0.02% NaN3, 1 M urea (filter and store at 4°C). <br><br> Soluble Aj3(l-40) peptide (Bachem, Torrance, CA) - 2.2 mg/mL in deionized H2O (stored in aliquots at -20°C, keep on ice when thawed) will self-seed after 1 week storage. Typically, the solution should be stored until no lag phase is seen in the assay. <br><br> 125l-labeledA(} (1-40) - 150K-350K cpm/jiL in 100% acetonitrile - 0.1% trifluoroacetic acid (TFA) - 1% J3-mercaptoethanol (aliquots stored at -20°C). 125i-iabeled Afi (1-40) can be made in accordance with the procedure set forth by H. LeVine, III in Neurobiol. Aging, 16, 755, (1995), which is hereby incorporated by reference, or this reagent may be purchased from Amersham, Arlington Heights, Illinois. <br><br> Final assay conditions: 30 (J.M soluble A/7 (1-40) in deionized water in assay buffer + 20K-50K cpm 125|_iatjeled A/3 (1-40) per assay. Compound to be tested is dissolved in dimethylsulfoxide (DMSO), typically 5 to 50 mM stock, such that the final concentration of DMSO is &lt;1% v/v in the assay. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -94- <br><br> Assay: Reaction mixture for 50 assays (on ice) is comprised of 0.1 to 0.2 |lL of <br><br> 125I-labeled A125I-labe!ed A0(1-40) + 1 \lL of soluble ^(1-40) + 13.5 M-L <br><br> assay buffer per assay. The following are the amounts of the components of the reaction mixture sufficient for 50 assay wells: <br><br> 5-10 jxL *25I-labeled Afi(lA0) dried down 675 jiL assay buffer 50 |j.L soluble A/3 (1-40) <br><br> Assay Method <br><br> 1) Prepare reaction mixture above by mixing components and storing on ice. <br><br> 2) Pipet 14.5 |lL of reaction mixture into each of 50 wells on a polypropylene U-bottom 96-well microtiter plate on ice. (Costar 3794). <br><br> 3) Add 1.7 p.L of diluted compound to be tested to each well in a column of eight, including solvent control. Serial 3-fold dilutions from 1 mM (100 |xM final) in assay buffer - urea = 7 dilutions + zero. Each 96-well plate can therefore accommodate 11 samples + 1 Congo Red control (0.039-5 |iM final in 2-fold steps). <br><br> 4) Seal the plate with aluminum film (Beckman 53 8619) and incubate for 10 minutes on ice. <br><br> 5) Raise the temperature to 37°C and incubate for 3 to 5 hours (depending on the lot of the peptide). <br><br> 6) Remove the aluminum film and add 200 pL/well of ice cold assay buffer with urea, collecting the radiolabeled fibrils by vacuum filtration through 0.2 |im pore size GVWP filters in 96-well plates (Millipore MAGV N22, Bedford, MA). Determine the radioactivity of the filters using standard methods well-known to those skilled in the art. <br><br> BASST (Beta-Amyloid Self-seeding. ThioflavinT) <br><br> An assay for inhibitors of self-seeded amyloid fibril growth <br><br> METHODS: <br><br> Materials: <br><br> Stock Solutions: <br><br> WO 00/76489 PCT/USOO/15071 <br><br> -95- <br><br> Assay Buffer - 50 xnM sodium phosphate, pH 7.5, 100 mM NaCl, 0.02% NaN3, 1 M urea (filter and store at 4°C) <br><br> Soluble Ap (1-40) - 2.2 mg/mL in deionized H2O (store in aliquots at -20°C, keep on ice when thawed) will self-seed after 1 week storage. Typically, the solution should be stored until no lag phase is seen in the assay. <br><br> Final assay conditions: 30 flM soluble Ap (1-40) in deionized water in assay buffer. Compound to be tested is dissolved in DMSO, typically 5 to 50 mM stock, such that the final concentration of DMSO is &lt;1% v/v in the assay. <br><br> Assay: Reaction mixture for 50 assays (on ice) comprised of 1 p.L of soluble AP( 1-40) + 13.5 (iL assay buffer per assay. The following are the amounts of the components of the reaction mixture that result in each of the 50 assay wells: 50 |iL soluble .4/2(1-40) <br><br> 675 {J.L assay buffer <br><br> Assay Method <br><br> 1) Prepare the reaction mix above by mixing the components and storing on ice. <br><br> 2) Pipet 14.5 fiL of reaction mixture into each of 50 wells of a polystyrene U-bottom 96-well microtiter plate (Coming 25881-96) on ice. <br><br> 3) Add 1.7 nL of diluted compound to be tested to each well in a column of eight, including solvent control. Serial 3-fold dilutions from 1 mM (100 fiM final) in assay buffer - urea = 7 dilutions + zero. Each 96-well plate can therefore accommodate 11 samples + 1 Congo Red control (0.039-5 |iM final in 2-fold steps). <br><br> 4) Seal the plate with aluminum film and incubate for 10 minutes on ice. <br><br> 5) Raise the temperature to 37°C and incubate for 3 to 5 hours (depends on the lot of the peptide). <br><br> 6) Remove the aluminum film and add 250 |iL/well of 5 p.M thioflavin T (ThT) [T-3516, Sigma-Aldrich] in 50 mM glycine-NaOH, pH 8.5. Read <br><br> WO 00/76489 PCT/US00/15071 <br><br> -96- <br><br> fluorescence on a plate reader (ex = 440 nm/20 nm ; em = 485 nm/20 nm) within 5 minutes. <br><br> BAPA (Beta-Amyloid Peptide Aggregation') <br><br> This assay is used to provide a measure of inhibition by a compound 5 against the aggregation behavior of the beta amyloid peptide. <br><br> The purpose of this assays is to provide a higher volume method of assaying the amount of beta amyloid aggregation using an endpoint assay based on filtration. In this assay, hexafluoroisopropanol (HFIP) is used to break down the initial amyloid peptide to a monomer state and use a concentration of 33 p.M 10 which is high enough so that aggregation will occur at pH 6.0 in several hours. <br><br> METHODS: <br><br> p-Amvloid Peptide Aggregation. pH 6.0 (BAPA") <br><br> In a 96-well plate (Costar 3794), we add 25 jiL 50 mM Phosphate Buffer, pH 6.0, 10 |xL 0.5 mg/mL Ap (1-40) peptide in 20% HFIP + 0.1 |J.L/assay 15 radioiodinated *25] (1-40) [125] Ap(l-40)], and 1 |xL of the compound to be tested starting at 50 mM with a concentration of DMSO &lt;1%. Then, we incubate for 2 to 4 hours at room temperature. We stop the reaction with 200 (xL of 50 mM phosphate buffer, pH 6.0, and filter it through a 0.2 fim 96-well filter plate (Millipore MAGIJ N22). We wash the filter plate with 100 jiL of the same 20 phosphate buffer. Aggregation was detected on a Microbeta counter after impregnating the filters with Meltilex (1450-441) and is corrected for background. <br><br> BATYM ASSAY <br><br> METHODS: <br><br> Required AP (1-42) (California Peptide) was dried from its 25 hexafluoroisopropanol (HFIP) stock solution. The AP (1-42) was dissolved in dimethylsulfoxide (DMSO) and then mixed with phosphate buffered saline (PBS) (pH 7.4). The mixed AP (1-42) solution was filtered with a 0.2 p.m Omnipore membrane syringe filter (Millipore, Bedford, MA). The compound to be tested in DMSO (50 times concentrate) was put into each well (0.5 (j.L/well) of a 96-well <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -97- <br><br> plate. The A(3 (1-42) solution was added into each well (24.5 |aL/well). The plate was centrifuged at 1,000 g for 5 minutes and incubated at 37°C for 1 day (Ap 1-42; final concentration 100 |iM). <br><br> After incubation Thioflavin T (ThT) (30 |J.M) solution in glycine-NaOH buffer (pH 8.5, 50 mM) was added into each well (250 jiL/well), fluorescence was measured (ex = 440/20 nm, em = 485/20 nm) using a fluorescence plate reader. The inhibitory activity was calculated as the reduction of fluorescence with the following formula: <br><br> Inhibition (%) = {(F(AP)-F(A|3+compound)} / {F( AP)-F(solvent + compound)} x 100 <br><br> The IC50S were calculated by a curve fitting program, using the following equation. The data were obtained from two different experiments in triplicate. <br><br> Inhibition(x) = 100-100/ {l+(x/IC5o)n}, <br><br> x = Concentration of tested compound (M), <br><br> IC50 = (M), <br><br> n = Hill coefficient. <br><br> Representative compounds of Formula I have exhibited inhibitory activities (IC50) ranging from 0.1 )lM to greater than 100 p.M in the foregoing assays. <br><br> The results of these assays for specific and representative compounds of the present invention are shown in Table 1 below. <br><br> WO 00/76489 PCT/US00/15071 <br><br> -98- <br><br> Tablc 1. P-Amyloid Inhibitory Activity of Compounds of Formula I <br><br> Example <br><br> BASSR <br><br> BASST <br><br> BATYM <br><br> BAPA <br><br> No. <br><br> o o <br><br> II <br><br> (IC50 = M-M) <br><br> (IC50 = M-M) <br><br> h-H <br><br> O <br><br> 0 II <br><br> 1 <br><br> W <br><br> 1 <br><br> 10 (P), &gt;100 (P) <br><br> 2, 4, 30,10 (P) <br><br> 50, 58.8 (P) <br><br> 60 (P), &gt;100 (P) <br><br> (6x), &gt;100 (Q), <br><br> 3(Q) <br><br> 57.8 (Q) <br><br> 86 (Q), <br><br> &gt;100 (R), <br><br> &gt;100 (R) <br><br> &gt;60 (R), <br><br> &gt;100 (S), <br><br> H(S),11(T) <br><br> &gt;60 (S), <br><br> 52 (T) <br><br> 6(Z) <br><br> 11 (T) <br><br> &gt;100 (Z) <br><br> 2 <br><br> 2.2,4.1,4.1, <br><br> 1, 1.5 (P) <br><br> 6.52 (P) <br><br> 70 (P) <br><br> 12,4.5 <br><br> 3 <br><br> 4.5, 5, 5 <br><br> 2 (P) <br><br> 11.7 (P) <br><br> &gt;60 (P) <br><br> (all 3 V-shaped) <br><br> 3 (Q) <br><br> (P) <br><br> 15 (ppt), 5 (Q) <br><br> 4 <br><br> 30, <br><br> 3,4,8 <br><br> 26.3,30.7 <br><br> 67 <br><br> &gt;100 (3x) <br><br> 5 <br><br> 70, &gt;100 <br><br> 4.5 <br><br> 10 <br><br> 74 <br><br> 6 <br><br> 15,21,20,40 <br><br> 4, 1,3 <br><br> 21.5 <br><br> &gt;60 <br><br> 7 <br><br> 18, 13, 12,20 <br><br> 2 <br><br> 8.83 <br><br> 39 <br><br> 8 <br><br> 15,15,18,15 <br><br> 3, &gt;100 <br><br> 7.17 <br><br> 9 <br><br> 20 (ppt), 30, <br><br> 1,2(P) <br><br> 20.1,28.2 (P) <br><br> 75 (P) <br><br> 52,40 (P) <br><br> 38.6 (R) <br><br> 10 <br><br> 70, 50 <br><br> 4 <br><br> 75.7 <br><br> 67 <br><br> 11 <br><br> 18 (ppt), <br><br> 1, 1,3(P) <br><br> 5.62 (P) <br><br> 23 (P) <br><br> 20 (ppt), <br><br> 1,0.8 (Q) <br><br> 6.78 (Q) <br><br> 9(Q) <br><br> 20 (2x), &gt;100 (P) <br><br> &gt;100,21, 30 (Q) <br><br> 12 <br><br> 20 (4x) <br><br> 1,1 <br><br> 3.93 <br><br> &gt;60 <br><br> 13 <br><br> 21, &gt;100, <br><br> 0.9 <br><br> 6.41 <br><br> 6 <br><br> 20 (ppt), <br><br> 15 (ppt), &gt;100 <br><br> 14 <br><br> 18 (ppt), 8, <br><br> 1.0 <br><br> 10.9 <br><br> &gt;10 <br><br> 6 (ppt), 7 (ppt) <br><br> (V-shaped) <br><br> 15 <br><br> 100 (3x)P <br><br> 1 (P) <br><br> 8.52 (P) <br><br> &gt;60 (P) <br><br> 100, 16 <br><br> 1.2 (Q) <br><br> 7.26 (Q) <br><br> 7(Q) <br><br> (V-shaped) <br><br> 7.07 (Q) <br><br> 12, 15, 11 (Q) <br><br> WO 00/76489 PCT/US00/15071 <br><br> -99- <br><br> Table 1. [3-Amyloid Inhibitory Activity of Compounds of Formula I (cont'd) <br><br> Example <br><br> BASSR <br><br> BASST <br><br> BATYM <br><br> BAPA <br><br> No. <br><br> (IC50 = P-M) <br><br> (IC50 = JiM) <br><br> (IC50 = ^M) <br><br> /»—N &gt;-* <br><br> 0 II <br><br> 1 <br><br> : S-X <br><br> 16 <br><br> 18, 7.5, 10(P) <br><br> 3, 0, 3 (P) <br><br> 12 (P) <br><br> 13 (P) <br><br> 70, 32,42 (Q) <br><br> 1.1,0.8, 0.6 (Q) <br><br> 10.3 (Q) <br><br> 17 <br><br> &gt;100 (ppt) (3x) <br><br> 6.2 <br><br> 64.5 <br><br> &gt;60 (Q), 41 (R) <br><br> 18 <br><br> &gt;100 (5x)(P) <br><br> 30, &gt;100 (P) <br><br> &gt;100(P) <br><br> 9, &gt;40, 53 (P), 12 <br><br> 19 <br><br> 3,4, &gt;100,2.2 <br><br> &gt;100, 1,1,1.5 <br><br> 31.0,34.0 <br><br> &gt;60,43 <br><br> 20 <br><br> 4.2 <br><br> 6 <br><br> 68.6 <br><br> 22 <br><br> 21 <br><br> 3 <br><br> 4 <br><br> 62.7 <br><br> 26 <br><br> 22 <br><br> 3 <br><br> 9 <br><br> &gt;100 <br><br> 24 <br><br> 23 <br><br> 20 <br><br> 2 <br><br> &gt;100 <br><br> 17 <br><br> 24 <br><br> &gt;100 <br><br> 20 <br><br> &gt;100 <br><br> 91 <br><br> 25 <br><br> &gt;100 <br><br> 4 <br><br> 21.1 <br><br> 47 <br><br> 26 <br><br> &gt;100 <br><br> 1 <br><br> &gt;100 <br><br> 57 <br><br> 27 <br><br> &gt;100 <br><br> 3 <br><br> 19.8 <br><br> 74 <br><br> 28 <br><br> &gt;100 <br><br> 5 <br><br> 42.3 <br><br> 27 <br><br> 29 <br><br> &gt;100 <br><br> 4 <br><br> 38.1 <br><br> 30 <br><br> 30 <br><br> 30, 20 <br><br> 4,2 <br><br> 75.3 <br><br> 38 <br><br> 31 <br><br> &gt;100 <br><br> 1 <br><br> 22.6 <br><br> 86 <br><br> 32 <br><br> &gt;100 <br><br> 1 <br><br> 29.2 <br><br> 96 <br><br> 33 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;10 <br><br> 34 <br><br> 45 <br><br> 3 <br><br> 45.0 <br><br> 48 <br><br> 35 <br><br> &gt;100 <br><br> 100 <br><br> &gt;100 <br><br> 154 <br><br> 36 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> 149 <br><br> 37 <br><br> &gt;100 <br><br> 0.8 <br><br> 30.2 <br><br> 25 <br><br> 38 <br><br> 20, 10 (V) <br><br> 3 <br><br> 23.4 <br><br> 184 <br><br> 39 <br><br> &gt;100 <br><br> 20 <br><br> &gt;100 <br><br> 21 <br><br> 40 <br><br> &gt;100 <br><br> 3.0 <br><br> &gt;100 <br><br> 53 <br><br> 41 <br><br> &gt;100 <br><br> 5 <br><br> 49.7 <br><br> 42 <br><br> 42 <br><br> &gt;100 <br><br> 2 <br><br> 55.6 <br><br> 30 <br><br> 43 <br><br> &gt;100 <br><br> 0.3 <br><br> 24.2 <br><br> 63 <br><br> 44 <br><br> &gt;100 <br><br> 1 <br><br> 26.5 <br><br> 52 <br><br> 45 <br><br> &gt;100 <br><br> 1 <br><br> 21.5 <br><br> 32 <br><br> 46 <br><br> &gt;100 <br><br> 6 <br><br> 34.3 <br><br> 47 <br><br> &gt;100 <br><br> 2 <br><br> 38.2 <br><br> 48 <br><br> 25 <br><br> 10 <br><br> &gt;100 <br><br> 49 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> 50 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> 51 <br><br> 85 <br><br> 0.8 <br><br> 39.1 <br><br> WO 00/76489 PCT/USOO/15071 <br><br> -100- <br><br> Table 1. ft-Amyloid Inhibitory Activity of Compounds of Formula I (cont'd) <br><br> Example <br><br> BASSR <br><br> BASST <br><br> BATYM <br><br> BAPA <br><br> No. <br><br> (IC50 = HM) <br><br> (IC50 = ^M) <br><br> (IC50 = HM) <br><br> (IC50 = RM) <br><br> 52 <br><br> 75 <br><br> 0.5 <br><br> 36.5 <br><br> 53 <br><br> &gt;100 <br><br> 0.3 <br><br> 30.0 <br><br> 54 <br><br> &gt;100 <br><br> 0.4 <br><br> 43.9 <br><br> 55 <br><br> 12 <br><br> 2 <br><br> 5.1 <br><br> 101 <br><br> 56 <br><br> &gt;100 <br><br> 3 <br><br> 11.5 <br><br> 30 <br><br> 57 <br><br> 4.8 <br><br> 1.5 <br><br> 4.0 <br><br> 50 <br><br> 58 <br><br> 3.5 <br><br> 1 <br><br> 5.1 <br><br> 60 <br><br> 59 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> 3 <br><br> 60 <br><br> &gt;100 <br><br> 3 <br><br> 40.7 <br><br> 8 <br><br> 61 <br><br> 18, 7.5, 10 <br><br> 3,0.3 <br><br> 12 <br><br> 13 <br><br> 62 <br><br> &gt;100 <br><br> 1.5 <br><br> 8.98 <br><br> 63 <br><br> 15, 15, 18 (ppt) <br><br> 1 <br><br> 9.43 <br><br> 45 <br><br> 64 <br><br> &gt;100 <br><br> 5 <br><br> 35 <br><br> &gt;100 <br><br> 65 <br><br> 60,80 <br><br> 1.5 <br><br> 15.9 <br><br> &gt;100 (V-shaped) <br><br> 66 <br><br> &gt;100 (ppt), <br><br> 2.1 <br><br> 50.1 <br><br> &gt;100 <br><br> &gt;100 (ppt) <br><br> 67 <br><br> 41 <br><br> 4 <br><br> 13.3 <br><br> &gt;60 <br><br> 68 <br><br> &gt;100, &gt;100 <br><br> 1 <br><br> &gt;100 <br><br> 110 <br><br> 69 <br><br> 2 (V-shaped), <br><br> 0.8 <br><br> 11.7 <br><br> 58 <br><br> 3.5 (ppt) <br><br> 70 <br><br> 20, 100 <br><br> 10 <br><br> &gt;100 <br><br> 65 <br><br> 71 <br><br> &gt;100 <br><br> 3 <br><br> &gt;60 <br><br> 72 <br><br> 40, 15, 12 <br><br> 2, 2.5 <br><br> 74.8 <br><br> &gt;60, &gt;60 <br><br> 73 <br><br> 25, 35, 40 <br><br> 0.3 <br><br> 9.43 <br><br> &gt;60 <br><br> 74 <br><br> 6,18,19,18 <br><br> 0.3,0.5 <br><br> 8.36 <br><br> &gt;60 <br><br> 75 <br><br> &gt;100 <br><br> 2.2 <br><br> 46.2 <br><br> &gt;60 <br><br> 76 <br><br> 3 <br><br> 0.5 <br><br> 8.59 <br><br> &gt;60 <br><br> 77 <br><br> 18, 15 <br><br> 8, 0.3 <br><br> 9.49 <br><br> &gt;60 <br><br> 78 <br><br> 70 <br><br> 0.1 <br><br> &gt;100 <br><br> 8 <br><br> 79 <br><br> 3.1,50,38, 70, <br><br> 1,0.3,0.3, 0.3 <br><br> 9.14 <br><br> 51 <br><br> 70, 30, 40 <br><br> 80 <br><br> &gt;100 <br><br> 4 <br><br> 24.8 <br><br> &gt;60 <br><br> 81 <br><br> &gt;100 <br><br> 15 <br><br> 48.4 <br><br> 73 <br><br> 82 <br><br> &gt;100, &gt;100, &gt;100 <br><br> 2, 0.3, 0.3 <br><br> 83 <br><br> &gt;100 <br><br> &gt;100 <br><br> 9,47, 29 <br><br> 84 <br><br> &gt;100 <br><br> &gt;100 <br><br> 5,40,21 <br><br> 85 <br><br> &gt;100 <br><br> 18 <br><br> 8, 77, 45 <br><br> WO 00/76489 PCT/US00/15071 <br><br> -101- <br><br> Table 1, ft-Amyloid Inhibitory Activity of Compounds of Formula I (cont'd) <br><br> Example <br><br> BASSR <br><br> BASST <br><br> BATYM <br><br> BAPA <br><br> No. <br><br> r-s <br><br> I <br><br> II <br><br> O lO <br><br> U <br><br> (IC5o = RM) <br><br> I <br><br> II <br><br> o in y <br><br> (IC50 = RM) <br><br> 86 <br><br> 40 <br><br> 18 <br><br> &gt;10, 89,37 <br><br> 87 <br><br> &gt;100 <br><br> 50 <br><br> &gt;10,15, 32 <br><br> 88 <br><br> &gt;100 <br><br> 10 <br><br> &gt;10, 37, 27 <br><br> 116 <br><br> &gt;100, &gt;100 <br><br> 18, 30 <br><br> 96 <br><br> 117 <br><br> &gt;100 <br><br> 3 <br><br> 61.3 <br><br> &gt;100 <br><br> 118 <br><br> &gt;100, &gt;100 <br><br> 6 <br><br> &gt;60 <br><br> 119 <br><br> &gt;100 <br><br> 3 <br><br> &gt;60 <br><br> 120 <br><br> &gt;100 <br><br> 3 <br><br> &gt;60 <br><br> 121 <br><br> &gt;100, &gt;100 <br><br> 1 <br><br> 122 <br><br> &gt;100 <br><br> 2 <br><br> &gt;100 <br><br> &gt;60 <br><br> 123 <br><br> &gt;100(3 x), 14 <br><br> 3,3 <br><br> 70.8 <br><br> 4, 18, &gt;100, <br><br> 3.2, 4 (Q) <br><br> 85.2 (Q) <br><br> &gt;60 (Q) <br><br> &gt;100 (Q) <br><br> 124 <br><br> &gt;100 <br><br> 10 <br><br> 62.7 <br><br> 125 <br><br> 82 <br><br> 10 <br><br> &gt;100 <br><br> 80 <br><br> 126 <br><br> &gt;100, &gt;100 <br><br> 4,5 <br><br> 84 <br><br> 63 <br><br> 30,100(Q) <br><br> 10,4 (Q) <br><br> 73.9 (Q) <br><br> &gt;60 (Q) <br><br> 127 <br><br> &gt;100 (ppt) <br><br> 10 <br><br> &gt;100 <br><br> 67 <br><br> 128 <br><br> &gt;100 (ppt) (4 x) <br><br> 10,41,6 <br><br> 75 <br><br> 60 <br><br> 11, &gt;100 (3 x) <br><br> 15, 20,10, 7.5 (Q) <br><br> 7, 3, 3 (Q) <br><br> &gt;60 (Q) <br><br> &gt;60 (Q) <br><br> 15, &gt;100 (3 x) Q <br><br> 129 <br><br> 1 (V-shaped) (2 <br><br> 10,3,2,2 <br><br> &gt;100 <br><br> &gt;102 <br><br> x) <br><br> &gt;100 (ppt) <br><br> 130 <br><br> &gt;100 (3 x) <br><br> 2, &gt;100, 50 <br><br> 47.5 <br><br> 238 <br><br> 131 <br><br> &gt;100 <br><br> 10 <br><br> 93.5 <br><br> &gt;60 <br><br> 132 <br><br> &gt;100 <br><br> 10 <br><br> &gt;100 <br><br> 60 <br><br> 133 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;60 <br><br> 134 <br><br> &gt;100 <br><br> 2 <br><br> 36.5 <br><br> &gt;60 <br><br> 135 <br><br> &gt;100 <br><br> 1.2 <br><br> 31.2 <br><br> &gt;60 <br><br> 136 <br><br> &gt;100 <br><br> 3 <br><br> &gt;100 <br><br> 53 <br><br> 137 <br><br> &gt;100, &gt;100 <br><br> 3 <br><br> 52 <br><br> 141 <br><br> &gt;100 <br><br> 7 <br><br> 56.7 <br><br> &gt;50 <br><br> 142 <br><br> &gt;100 <br><br> 2.1 <br><br> 26.9 <br><br> 55 <br><br> 143 <br><br> &gt;100 (4 x) <br><br> 40,30 <br><br> &gt;100 <br><br> 2, &gt;60, &gt;60 <br><br> 144 <br><br> 15, 25 <br><br> 40 <br><br> &gt;100 <br><br> 114 <br><br> WO 00/76489 PCT/US00/15071 <br><br> -102- <br><br> Table 1. p-Amyloid Inhibitory Activity of Compounds of Formula I (cont'd) <br><br> Example <br><br> BASSR <br><br> BASST <br><br> BATYM <br><br> BAPA <br><br> No. <br><br> (IC50 = RM) <br><br> ✓—\ 5 <br><br> t <br><br> 0 II <br><br> •w <br><br> 1 <br><br> (IC50 = RM) <br><br> (ic50 = M-M) <br><br> 145 <br><br> 10,40, 30 <br><br> 4 <br><br> 56.8 <br><br> 9 <br><br> 146 <br><br> &gt;100 <br><br> 30 <br><br> &gt;100 <br><br> &gt;60 <br><br> 147 <br><br> &gt;100 <br><br> 10 <br><br> 93.4 <br><br> &gt;60 <br><br> 148 <br><br> &gt;100 <br><br> &gt;100 <br><br> 149 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;100 <br><br> &gt;60 <br><br> 150 <br><br> &gt;100 <br><br> 10 <br><br> &gt;100 <br><br> 76 <br><br> 151 <br><br> &gt;100, &gt;100 <br><br> 5, &gt;100 <br><br> &gt;100 <br><br> 108 <br><br> 154 <br><br> &gt;100 <br><br> 3,30 <br><br> 70.8 <br><br> 155 <br><br> &gt;100 <br><br> 3 <br><br> 44.6 <br><br> 156 <br><br> 27.8 <br><br> 157 <br><br> 25.9 <br><br> A letter in parentheses after particular value indicates the particular synthetic lot of the compound tested. The terms "P," "Q," "R," "S," "T," and "Z" designate different lots of the same compound. For example, 10 (P) indicates that compound tested was from Lot P. If no lot is specified, the lot of the compound 5 was Lot P. <br><br> The abbreviation "ppt" means precipitate and indicates that a precipitate formed at the indicated concentration. In addition, the term "V-shaped" means that inhibition was observed followed by precipitation. <br><br> A value followed by a number and x (i.e., 4x) means that the compound 10 was tested four times, and each time the result was the same. <br><br> The invention compounds have also shown good activity in standard in vivo assays commonly used to evaluate agents to treat diseases related to aggregation of amyloid proteins, especially Alzheimer's disease and other amyloidoses. In one assay, amyloid protein is induced into the spleen of mice by 15 subcutaneous injections of silver nitrate, Freund's complete adjuvant, and an intravenous injection of amyloid enhancing factor. Silver nitrate is administered each day through Day 11. Test compounds are administered to the mice daily starting on Day 1 through Day 11. On Day 12, the animals are sacrificed, and the spleens are removed, histologically prepared, stained with Congo red, and the 20 percent area of the spleen occupied by birefringent, Congo red-stained amyloid is <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -103- <br><br> quantitated microscopically. Invention compounds evaluated in this test have inhibited splenic amyloid deposition by up to 70% relative to untreated controls. <br><br> Another in vivo assay in which the invention compounds have been evaluated uses transgenic mice. The mice bear a human p-amyloid precursor protein transgene with a prion promoter and are described by Hsiao et al., "Correlative memory deficits, Ap elevation, and amyloid plaques in transgenic mice," Science 1966;274:99-102. These transgenic mice develop (3-amyloid deposits at about 9 months of age. By 15 months, diffuse and compact senile plaques are abundant, primarily in the neocortex, olfactory bulb, and hippocampus. Invention compounds are administered orally to the mice beginning at the age of 8 months (just prior to the onset of amyloid deposits) and continuing for several months (up to about age 14-18 months). The animals are then sacrificed, and the brains are removed. The amount of amyloid in the brain is quantitated both histologically and biochemically. Invention compounds evaluated in this model have inhibited amyloid accumulation in the cortex and hippocampus by up to 49% relative to untreated controls. <br><br> The above data establishes that representative invention compounds are active in standard assays used to measure inhibition of protein aggregation. The compounds exhibit excellent specificity, for example, as shown in the BASST assay, as well as the BATYM and BAPA assays. The compounds are thus useful to clinically inhibit amyloid protein aggregation and to image amyloid deposits for diagnostic use. The compounds will be used in the form of pharmaceutical formulations, and the following examples illustrate typical compositions. <br><br> WO 00/76489 <br><br> PCT/US00/15071 <br><br> -104-EXAMPLE 164 <br><br> Tablet Formulation <br><br> Ingredient <br><br> Amount <br><br> Compound of Example 1 <br><br> 50 mg <br><br> Lactose <br><br> 80 mg <br><br> Cornstarch (for mix) <br><br> 10 mg <br><br> Cornstarch (for paste) <br><br> 8 mg <br><br> Magnesium Stearate (1%) <br><br> 2 mg <br><br> 150 mg <br><br> The compound of Example 1 is mixed with the lactose and cornstarch (for mix) and blended to uniformity to a powder. The cornstarch (for paste) is suspended in 6 mL of water and heated with stirring to form a paste. The paste is added to the mixed powder, and the mixture is granulated. The wet granules are passed through a No. 8 hard screen and dried at 50°C. The mixture is lubricated with 1% magnesium stearate and compressed into a tablet. The tablets are administered to a patient at the rate of 1 to 4 each day for prevention of amyloid protein aggregation and treatment of Alzheimer's disease. <br><br> EXAMPLE 165 <br><br> Parenteral Solution <br><br> In a solution of 700 mL of propylene glycol and 200 mL of water for injection is added 20.0 g of Compound No. 19 (Example 19). The mixture is stirred and the pH is adjusted to 5.5 with hydrochloric acid. The volume is adjusted to 1000 mL with water for injection. The solution is sterilized, filled into 5.0 mL ampoules, each containing 2.0 mL (40 mg of Compound No. 19), and sealed under nitrogen. The solution is administered by injection to a patient suffering from medullary carcinoma of the thyroid and in need of treatment. <br><br></p> </div>

Claims (1)

  1. <div class="application article clearfix printTableText" id="claims"> <p lang="en"> WO 00/76489<br><br> PCT/US00/15071<br><br> -105-EXAMPLE 166<br><br> Patch Formulation<br><br> Ten milligrams of 2-{4-[3-(3,4-dichlorophenyl)propyl]phenylamino} benzoic acid is mixed with 1 mL of propylene glycol and 2 mg of acrylic-based 5 polymer adhesive containing a resinous cross-linking agent. The mixture is applied to an impermeable backing (30 cm2) and applied to the upper back of a patient for sustained release treatment of amyloid polyneuropathy.<br><br> The invention and the manner and process of making and using it, are now described in such full, clear, concise, and exact terms as to enable any person 10 skilled in the art to which it pertains, to make and use the same. It is to be understood that the foregoing describes preferred embodiments of the present invention and that modifications may be made therein without departing from the spirit or scope of the present invention as set forth in the claims. To particularly point out and distinctly claim the subject matter regarded as invention, the 15 following claims conclude this specification.<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -106-CLAIMS<br><br> What is claimed is:<br><br> 1. The use of a compound of Formula I<br><br> 10<br><br> 15<br><br> 20<br><br> R<br><br> ji R<br><br> /Vn<br><br> • R&lt;<br><br> la wherein<br><br> R<br><br> O<br><br> R<br><br> Ra is hydrogen, Cj-Cg alkyl, or -CCj-Cg alkyl;<br><br> n is 1 to 5 inclusive;<br><br> Rl, R2, R^, r4 r5? r65 and r7 gjg independently hydrogen, halogen,<br><br> -OH, -NH2, NRbRc, -C02H, -C02C]-C6 alkyl, -N02, -OCi-C12 alkyl, -C^-Cg alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyl, -O-phenyl, -O-substituted phenyl,<br><br> 0 O<br><br> 1 K<br><br> -CHCH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb -NH(CH2)pNRbRc, -N(C 1 -C6alkyl)(CH2)pNRbRc,<br><br> yCH2OCj-Cg alkyl " ' J<br><br> —CH -<br><br> ^CH2OCj-C6alkyl ^<br><br> R8 is COOH, tetrazolyl, -S02Rd, or -C0NHS02Rd; "■<br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m-phenyl, or<br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl,<br><br> -107-<br><br> imidazolyl, piperazinyl, 4-C]-Cg alkylpiperazinyl, morpholino, thiomorpholino, decahydroisoqurnoline, or pyrazolyl;<br><br> Rd is hydrogen, -Cj-Cg alkyl, -CF3, or phenyl;<br><br> m is 0 to 5 inclusive;<br><br> p is 1 to 5 inclusive;<br><br> A is CH orN;<br><br> Rl and R-, when adjacent to one another, can be methylene-dioxy;<br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for treating Alzheimer's disease.<br><br> The use of Claim 1 wherein Ra is hydrogen;<br><br> n is 2; and<br><br> R3 and R^ are hydrogen.<br><br> The use of Claim 1 wherein Ra is hydrogen;<br><br> R^ and R^ are hydrogen; and n is 2 to 5 inclusive.<br><br> The use of Claim 1 wherein Ra is hydrogen;<br><br> n is 2;<br><br> R^ and R^ are hydrogen; and<br><br> Rl, R2, and R^ are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -CF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl,<br><br> , -N[(CH2)3CH3]2, substituted phenyl,<br><br> -OCH2- substituted phenyl, pyrrozolyl, or -N(phenyl)2-<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -108-<br><br> 5. The use of Claim 1 wherein Ra is hydrogen;<br><br> n is 3, 4, or 5;<br><br> and R^ are hydrogen; and Rl, R2, and R? are independently chlorine or hydrogen.<br><br> 6. The use of Claim 1 wherein Ra is hydrogen;<br><br> nis 2;<br><br> R3 and R^ are hydrogen; and<br><br> R^, r65 and R8 are independently hydrogen, -CO2H, -NO2, -OCH3, imidazolyl, -CN, fluorine, -CH3, -CF3, halogen,<br><br> -NH-C j-Cg alkyl,-NCC j-Cgalkyl)^, -NH2, or pyrrolyl<br><br> 7. The use of Claim 1 wherein Ra is hydrogen;<br><br> n is 2;<br><br> R^ and R^ are hydrogen; and R5 is -C02H.<br><br> I<br><br> 8. The use of a compound of Formula I<br><br> wherein<br><br> Ra is hydrogen; n is ] to 5 inclusive;<br><br> -109-<br><br> and are hydrogen;<br><br> Rl, R^, and R2 are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -OF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, -N[(CH2)3CH3]2, substituted phenyl, -OCH2~substituted phenyl, pyrazolyl, or -N(phenyl)2;<br><br> R^ and are independently hydrogen, -CO2H, -N02, -OCH3,<br><br> imidazolyl, -CN, fluorine, -CH3, -CF3, or pyrrolyl;<br><br> R8 is COOH or tetrazolyl;<br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for treating Alzheimer's disease.<br><br> The use of Claim 1 wherein the compound of Formula I is:<br><br> 2-[[4-[2-(3,4-Dichlorophenyl)ethyl]phenyl]amino-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino}-5-nitrobenzoic acid;<br><br> 2-{4-[4-(3,4-Dichloro-phenyl)-ethyl]phenylamino}-4-methoxy-5-nitrobenzoic acid;<br><br> 2-{4-[2-(3,4-Dihydroxy-phenyl)-ethyI]-phenylamino}benzoic acid; 2- {4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino } benzoic acid; 2- {4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino } benzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid;<br><br> 2- {4-[3 -(3,4-Dichl orophenyl)propyl]phenylamino } -4-imidazo-l-yl-5-nitrobenzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)-propyl]phenylamino}benzoic acid; 2-{4-[4-(3,4-Dichlorophenyl)butyl]phenylamino}benzoic acid; 2- {4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamino } -5-nitrobenzoic acid;<br><br> 00/76489 PCT/US00/1S071<br><br> -110-<br><br> 2-{4-[4-(3,4-Dichlorophenyl)-butyl]phenylamino}-3,5-dinitrobenzoic acid;<br><br> 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic acid;<br><br> 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid;<br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino]-benzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid; 2-(4-Phenethyl-phenylamino)-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -terephthalic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoicacid;<br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino }-5-methanesulfonyl-benzoic acid;<br><br> 2 - {4- [2-(3,4-Dichloro-phenyI)-ethyl]-phenylamino } -5 -imidazol-1 -yl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-nitro-benzoic acid;<br><br> 00/76489 PCT/US00/15071<br><br> -111-<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -3 -nitrobenzoic acid;<br><br> 5-Cyano-2-{4-[2-(3,4-dichloro-phenyl)-etbyl]-phenylamino}-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -4,6-difluoro-benzoic acid;<br><br> 6- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -2,3 -difluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-fluoro-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl] -phenylamino } -3-fluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-methyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-fluoro-benzoic acid;<br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -3, 5-difluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifluoromethyl-benzoic acid;<br><br> 2- {4- [2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -6-trifluoromethyl-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -5-trifluoromethyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-pyrrol-l-yl-benzoic acid;<br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[4-(3-Dimethylamino-propoxy)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 00/76489<br><br> PCT/US00/15071<br><br> -112-<br><br> 2-(4- {2-[4-(2-Ethoxy-1 -ethoxymethyl-ethyl)-phenyl] -ethyl} -phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Pyrrol-l -yl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2- {4-[2-(4-Styryl-phenyl)-ethyl] -phenylamino } -benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2- { 4-[2-(4'-Ethyl-biphenyl-4-yl)-ethyl] -phenylamino } -benzoic acid;<br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyI]-phenylamino}-benzoic acid; 2-(4-{2-[3-(3,5-Dichloro-phenoxy)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-(4- {2-[4-(2-Chloro-6-fluoro-benzyloxy)-phenyl]-ethyl} -phenylamino)-benzoic acid;<br><br> 2- {4-[2-(4-Pyrazol-1 -yl-phenyl)-ethyl]-phenylamino} -benzoic acid;<br><br> 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-(4- {2- [4-(3,4-Dichloro-benzyloxy)-phenyl] -ethyl} -phenylamino)-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-amino-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichlorophenyl)]phenylamino}-5-nitrobenzoic acid; 2-{4-[3-(3,4-Dichlorophenyl)propyI]phenylamino}-5-nitrobenzoic acid;<br><br> 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl] phenylamino} -5-nitrobenzoic acid;<br><br> 2-[[4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenyl]amino-benzoic acid; or<br><br> 2-[4-(3,4-Dichlorophenyl)phenyl]aminobenzoic acid.<br><br> WO 00/76489<br><br> -113-<br><br> 10. The use of a compound of Formula I<br><br> PCT/US00/15071<br><br> 10<br><br> 15<br><br> 20<br><br> 25<br><br> R<br><br> wherein<br><br> RJ //\<br><br> R-<br><br> JO-<br><br> (CH2):<br><br> ■N-<br><br> R<br><br> R<br><br> .R<br><br> R<br><br> R*<br><br> O<br><br> Ra is hydrogen, Cj-Cg alkyl, or -CCj-Cg alkyl;<br><br> n is 0 to 5 inclusive;<br><br> Rl, R2, RJ, r4, r5? r6; and are independently hydrogen, halogen,<br><br> -OH, -NH2, NRbRc, -C02H, -C02C]-C6 alkyl, -N02, -OC]-C12 alkyl, -Ci-Cg alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyl, -O-phenyl, -O-substituted phenyl,<br><br> O O<br><br> D fl<br><br> -CH=CH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C j -Cgalkyl)(CH2)pNRbRc,<br><br> /^OCj-Cg alkyl<br><br> —CH \<br><br> CH2OCrC6 alkyl r8 is COOH, tetrazolyl, -S02Rd, or -C ONHS 02Rd;<br><br> Rb and Rc are independently hydrogen, -C}-Cg alkyl, -(CH^m-phenyl, or<br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-Cj-Cg alkylpiperazinyl, morpholino,<br><br> thiomorpholino, decahydroisoquinoline, or pyrazolyl;<br><br> 2<br><br> Lvvi<br><br> Rd is hydrogen, -C]-Cg alkyl, -CF3, or phenyl;<br><br> m is 0 to 5 inclusive;<br><br> p is 1 to 5 inclusive;<br><br> A is CH orN;<br><br> Rl and R2, when adjacent to one another, can be methylene-dioxy; or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for inhibiting the aggregation of amyloid proteins to form amyloid deposits.<br><br> The use of Claim 10 wherein<br><br> Ra is hydrogen;<br><br> n is 2; and r3 and are hydrogen.<br><br> The use of Claim 10 wherein RaTs~Hydrogeh;<br><br> r3 and R^ are hydrogen; and n is 2 to 5 inclusive.<br><br> The use of Claim 10 wherein Ra is hydrogen;<br><br> n is 2;<br><br> R^ and R^ are hydrogen; and<br><br> Rl, R2, and R"? are independently chlorine, -N(CH2CH3)2, -OH, CH3-fluorine, -CF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2&gt;3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH20CH2CH3)2, pyrrolyl, -CH=CH-phenyl,<br><br> , -N[(CH2)3CH3]2- substituted phenyl,<br><br> -OCH2-substituted phenyl, pyrazolyl, or -N(phenyl)2.<br><br> The use of Claim 10 wherein<br><br> WO 00/76489 PCT/USO0/15071<br><br> -115-<br><br> Ra is hydrogen;<br><br> n is 3, 4, or 5;<br><br> r3 and R^ are hydrogen; and<br><br> Rl, R2, and are independently chlorine or hydrogen.<br><br> 15. The use of Claim 10 wherein Ra is hydrogen;<br><br> n is 2;<br><br> R^ and R^ are hydrogen; and r5 and R^ are independently hydrogen, -CO2H, -NO2, -OCH3, imidazolyl, -CN, fluorine, -CH3, -CF3, halogen, -NH-C]-C6 alkyl, -N(C]-Cgalkyl)2, -NH2, or pyrrolyl.<br><br> 16. The use of Claim 10 wherein Ra is hydrogen;<br><br> n is 2;<br><br> r3 and R^ are hydrogen; and R8 is -C02H.<br><br> 17. The use of a compound of Formula I<br><br> wherein<br><br> Ra is hydrogen;<br><br> n is 1 to 5 inclusive;<br><br> -116-<br><br> R-3 and R^ are hydrogen;<br><br> Rl, R?, and R- are independently chlorine, -N(CH2CH3)2, -OH, CH3-, fluorine, -GF3, phenyl, hydrogen, -OCH2 phenyl, -0(CH2)3N(CH3)2, -O phenyl, -0(CH2)7CH3, -CH(CH2OCH2CH3)2, pyrrolyl, -CH=CH-phenyl, -N[(CH2)3CH3]2, substituted phenyl, -OCH2-substituted phenyl, pyrazolyl, or -N(phenyl^;<br><br> R5 and R^ are independently hydrogen, -CO2H, -NO2, -OCH3,<br><br> imidazolyl, -CN, fluorine, -CH3, -CF3, or pyrrolyl;<br><br> R8 is COOH or tetrazolyl;<br><br> A is CH orN;<br><br> Rl and R2, when adjacent to one another, can be methylene-dioxy;<br><br> or the pharmaceutically acceptable salts thereof, in the manufacture of a medicament for inhibiting the aggregation of amyloid proteins to form amyloid deposits.<br><br> The use of Claim 17 wherein the compound of Formula I is:<br><br> 2-[[4-[2-(3,4-Dichlorophenyl)ethyl]phenyl]amino-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]phenylamino}-5-nitrobenzoic acid;<br><br> 2- {4-[4-(3,4-Dichloro-pheny l)-ethyl]phenylamino } -4-methoxy-5-nitrobenzoic acid;<br><br> 2- {4- [2-(3,4-Dihydroxy-phenyl)-ethyl]-phenylamino} benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]phenylamino}benzoic acid; 2-{4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino}benzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-methoxy-5-nitrobenzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-imidazo-1 -yl-5-nitrobenzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)-propyl]phenylamino}benzoic acid; 2- {4-[4-(3,4-Dichlorophenyl)butyl]phenylamino } benzoic acid;<br><br> 00/76489<br><br> PCT/US00/15071<br><br> -117-<br><br> 2- {4- [4-(3,4-Dichloro-phenyl)-butyl] -phenylamino } -5-nitrobenzoic acid;<br><br> 2- {4- [4-(3,4-Dichlorophenyl)-butyl]phenylamino} -3,5-dinitrobenzoic acid;<br><br> 2-{4-[5-(3,4-Dichlorophenyl)pentyl]phenylamino}-5-nitrobenzoic acid;<br><br> 2- {4- [5-(3,4-Dichloro-phenyl)pentyl]phenylamino } -4-methoxy-5-nitrobenzoic acid;<br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino]-benzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid; 2-(4-Phenethyl-phenylamino)-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl] -phenylamino } -terephthalic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic acid;<br><br> 4- {4- [2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -isophthalic acid;<br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl] -phenylamino } -5-methanesulfonyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino }-5-imidazol-1 -yl-benzoic acid;<br><br> 2- (4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -6-nitro-benzoic acid;<br><br> 00/76489<br><br> PCT/USOO/15071<br><br> -118-<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-nitro-benzoic acid;<br><br> 5-Cyano-2-{4-[2-(3,4-dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4,6-difluoro-benzoic acid;<br><br> 6- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -2,3 -difluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-fluoro-benzoic acid;<br><br> 2-{4-[2~(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-fluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-methyl-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino} -4-fluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3,5-difluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifluoromethyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-6-trifluoromethyl-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl] -phenylamino } -5-trifluoromethyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-pyrrol-l-yl-benzoic acid;<br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-(4-{2-[4-(3-Dimethylamino-propoxy)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -119-<br><br> 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[4-(2-Ethoxy-l-ethoxymethyl-ethyl)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2- {4-[2-(4-Pyrrol-1 -yl-phenyl)-ethyl] -phenylamino } -benzoic acid; 2-{4-[2-(4-Styryl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(4/-Ethyl-biphenyl-4-yl)-ethyl]-phenylamino}-benzoic ^10 acid;<br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4- { 2- [3 -(3,5-Dichloro-phenoxy)-phenyl] -ethyl} -phenylamino)-benzoic acid;<br><br> 2-(4- { 2- [4-(2-Chloro-6-fluoro-benzyloxy)-phenyl]-ethyl} -15 phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Pyrazol-1 -yI-phenyl)-ethyl]-phenylamino} -benzoic acid;<br><br> 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 20 2-(4- (2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethyl} -<br><br> phenylamino)-benzoic acid;<br><br> 2- {4-[2- [(3,4-Dichlorophenyl)propyl]phenylamino } -5-nitrobenzoic acid;<br><br> 2- {4- [2-(3,4-Dimethyl-phenyl)-ethyl] phenylamino } -5 -25 nitrobenzoic acid;<br><br> 2-[ [4-[2-(4-Chloro-3-trifluoromethy Ipheny l)ethy 1] phenyl] amino-benzoic acid; or<br><br> 2-[4-(3,4-Dichlorophenyl)phenyl]aminobenzoic acid.<br><br> 19. The compounds: 30 2- {4-[4-(3,4-Dichloro-phenyl)-ethyl]phenylamino } -4-methoxy-<br><br> 5-nitrobenzoic acid;<br><br> 2-{4-[2-(3,4-Dihydroxy-pheny])-ethyl]-phenylaminojbenzoic acid;<br><br> 00/76489<br><br> PCT/USO0/15071<br><br> -120-<br><br> 2- {4- [2-(4-Dibutylamino-phenyl)-ethyl]phenylamino} benzoic acid; 2-{4-[2-(3,4,5-Trihydroxy-phenyl)-ethyl]phenylamino}benzoic acid;<br><br> 2- {4- [3 -(3,4-Dichlor ophenyl)propyl]phenylamino } -4-methoxy-5-nitrobenzoic acid;<br><br> 2-{4-[3-(3,4-Dichlorophenyl)propyl]phenylamino}-4-imidazo-l-yl-5-nitrobenzoic acid; or<br><br> 2-{4-[4-(3,4-DichlorophenyI)butyl]phenylamino} benzoic acid.<br><br> The compounds:<br><br> 2- {4-[4-(3,4-Dichloro-phenyl)-butyl] -phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[4-(3,4-Dichlorophenyl)-butyl]phenylamino}-3,5-dinitrobenzoic acid;<br><br> 2 - {4-[5-(3,4-Dichlorophenyl)pentyl] phenylamino } -5 -nitrobenzoic acid;<br><br> 2-{4-[5-(3,4-Dichloro-phenyl)pentyl]phenylamino}-4-methoxy-5-nitrobenzoic acid; .<br><br> 2-[4-(3,4-Dichloro-benzyl)-phenylamino]-benzoic acid; 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2- {4- [2-(4-Chloro-3 -trifluoromethyl-phenyl)-ethyl] -phenylamino } -benzoic acid;<br><br> 2-[4-(2-Biphenyl-4-yl-ethyl)-phenylamino]-5-nitro-benzoic acid; 5-Nitro-2-(4-phenethyl-phenylamino)-benzoic acid. 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-amino-benzoic acid;<br><br> 2- {4-{2-(3,4-Dichloro-pheny l)-ethy l]-phenylamino } -5-trifluoromethyl-benzoic acid.<br><br> WO 00/76489 PCT/US00/15071<br><br> -121-<br><br> 21. The compounds:<br><br> 2-(4-Phenethyl-phenylamino)-benzoic acid; 2-{4-[2-(3,4-Dichloro-pheny])-ethyl]-phenylamino} -5-methoxy-benzoic acid;<br><br> 5 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-terephthalic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methyl-benzoic acid;<br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic<br><br> ^^0 acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -5 -methanesulfonyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-imidazol-l-yl-benzoic acid;<br><br> 15 2-{4-[2-(3,4-Dichloro-pheny l)-ethyl] -phenylamino } -6-nitro-<br><br> benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-nitro-benzoic acid; or<br><br> 2-{4-[2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino}-3-nitro-20 benzoic acid.<br><br> The compounds:<br><br> 5-Cyano-2-{4-[2-(3,4-dichloro-phenyl)-ethyl]-phenyIamino}-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4,6-difluoro-benzoic acid;<br><br> 6- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -2,3-difluoro-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -6-fluoro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-fluoro-benzoic acid;<br><br> 22.<br><br> 25<br><br> 30<br><br> 00/76489<br><br> PCT/US00/15071<br><br> -122-<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -3 -methyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-4-fluoro-benzoic acid;<br><br> 2-{4- [2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -3,5-difluoro-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -3-trifluoromethyl-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-pheny l)-ethyl]-pheny lamino} -6-trifluoromethyl-benzoic acid;<br><br> 2-{4-[3-(4-Diethylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Nitrophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Nitrophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Aminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Aminophenyl)propyl]phenylamino}benzoic acid; 2- {4- [2-(4-Aminophenyl)phenylamino} benzoic acid; 2- {4- [2-(4-Dipropylaminophenyl)ethyl]phenylamino } benzoic acid monohydrochloride;<br><br> 2 - {4-[2-(4-DiethylaminophenyI)ethyl]phenylamino } benzoic acid monohydrochloride monohydrate;<br><br> 2-{4-[3-(3 -Dipropylaminophenyl)propyl] phenylamino } benzoic acid;<br><br> 2-{4-[3-(3-Dimethylaminophenyl)propyl]phenylamino}benzoic acid;<br><br> 2-{4-[3-(4-Ethylaminophenyl)propyl]phenylamino}benzoic acid; 2-(N-{4-[3-(4-Diethylaminophenyl)propyl]phenyl}-N-ethylamino)benzoic acid;<br><br> 2-{4-[2-(3-Dibenzylaminophenyl)ethyl]phenylamino}benzoic acid; 2- {4-[3-(3 -DiethyIaminophenyl)propyl]phenylamino } benzoic acid; 2-{4-[2-(3-Aminophenyl)ethyl]phenylamino}benzoic acid; 2-{4-[3-(4-Dimethylaminophenyl)propyl]phenylamino}benzoic acid;<br><br> 2- {4- [2-(4-Acetylaminophenyl)ethyl]phenylamino} benzoic acid;<br><br> 00/76489<br><br> PCT/USOO/15071<br><br> -123-<br><br> 2- {4-[2-(3 -Acetylaminophenyl)ethyl]phenylamino} benzoic acid; 2-{4-[2-(3-Dipropylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride;<br><br> 2-{4-[2-(3-Dibutylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride;<br><br> 2-{4-[3-(4-Acetylaminophenyl)propyl]phenylamino}benzoic acid; 2- {4-[3-(3-Acetylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[2-(3-Diethylaminophenyl)ethyl]phenylamino}benzoic acid monohydrochloride;<br><br> 2- {4-[2-(3 -Piperidin-1 -ylphenyl)ethyl]phenylamino} benzoic acid monohydrochloride;<br><br> 2-{4-[3-(4-Dipropylaminophenyl)propyl]phenylamino}benzoic acid;<br><br> 2-{4-[3-(4-Dibutylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(3-Dibutylaminophenyl)propyl]phenylamino}benzoic acid; 2-(4-{3-[4-(lH-Pyrrol-l-yl)phenyl]propyl}phenylamino)benzoic acid;<br><br> 2-{4-[3-(4-Piperidin-l-ylphenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Diethylcarbamoylphenyl)propyl]phenylamino}benzoic acid;<br><br> 2-{4-[3-(4-Carboxyphenyl)propyl]phenylamino}benzoic acid; 2- { 4- [3 -(4-Diethylaminomethylpheny l)propyl]phenylamino } benzoic acid;<br><br> 2-{4-[3-(4-Propylaminophenyl)propyl]phenylamino}benzoic acid; 2- {4-[3 -(3-Propylaminophenyl)propyl]phenylamino}benzoic acid; 2-{4-[3-(4-Pyrrolidin-l-yl-phenyl)-propyl]-phenylamino}-benzoic acid;<br><br> 2- {4- [3 -(3 -Piperidin-1 yl-phenyl)-propyl]-phenylamino} -benzoic acid;<br><br> 00/76489<br><br> PCT/USO0/15071<br><br> -124-<br><br> 4- { 5-[( 1 -Butyl-1,2,3,4-te1xahydroquinolin-6-yl)rnethylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}butanoic acid;<br><br> 2- {4-[3 -(3,4-Di cruoro-phenyl)-propyl]phenylamino } -5-methyl-benzoic acid;<br><br> N-(2- {4-{3 -(3,4-Dichloro-phenyl)-propyl]-phenylamino } -benzoyl )-methanesulofeamixae;<br><br> 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl]phenylamino}-5-nitro-benzoic acid;<br><br> 2- [4-(2-Biphenyl-4-yl-ethyl)-pheny lamino] - 5-nitro-benzoic acid; 2-{4-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethyl]-phenylainino}-5-nitro-benzoic acid;<br><br> 5-Airano-2-{4-[2-(3,4-DicUoro-phenyl)-ethyl]-phenylammo}-benzoic acid;<br><br> 5-Nitro-2-(4-phenethyl-phenylamino}-benzoic acid; 2-{4-[2-(4-Fluoro-3-trifluoromethyl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(3,4-Difluoro-phenyl)-ethyl]-phenylamino}-5-nitrobenzoic acid;<br><br> {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyl}-[2-( 1 H-tetrazol-5-yl)-phenyl]-amine;<br><br> 2-{4-[2-(4-Fluoro-3-trifluoromethyl-phenyl)-ethyl]-phenylarmno } -5-nitro-benzoic acid;<br><br> 2-(4-Phenethyl-phenylamino)-benzoic acid; 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino} -5-fluoro-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl] -phenylamino } -nicotinic acid; 2-{4-[2-(3-Chloro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(4-Chloro-phenyl)-ethyl]-phenylaniino}-5-nitro-benzoic acid;<br><br> 00/76489<br><br> PCT/USOO/15071<br><br> -125-<br><br> 2-{4-[2-(3,4-Di chl oro-pheny l)-ethyl] -phenylamino } -5-methyl-benzoic acid;<br><br> 2- {4-[2-(2-Chloro-phenyl)-ethyl] -phenylamino } -5-nitro-benzoic acid;<br><br> 2-{4-[2-(2,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2- {4- [2-(3,4-Dichl oro-phenyl)-ethyl]-phenylamino } -6-trifhioromethyl-benzoic acid;<br><br> 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-dimethylamino-benzoic acid;<br><br> 2-{4-[2-(3,5-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4- {2- [(4aS, 8aR)-4-(Octahydro-isoquinolin-2-yl)-phenyl] -ethyl} -phenylamino)-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 3- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino } -benzoic acid; 5-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-isophthalic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(3,4-Dichloro-pheny l)-ethyl]-phenylamino} -4,5-dimethoxy-benzoic acid;<br><br> 2-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyI]-phenylamino}-3-nitro-benzoic acid;<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -126-<br><br> 3-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 5- {4-[2-(3 -Chloro-4-methyl-phenyl)-ethyl] -phenylamino } -isophthalic acid;<br><br> 5 2- {4-[2-(3 -Chloro-4-methyl-phenyl)-ethyl] -phenylamino } -benzoic acid;<br><br> 4-(4-{2-[(4aS,8aR)-4-(Octahydro-isoquinolin-2-yl)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-5-10 methoxy-benzoic acid;<br><br> 2-{4-[2-(3-Methoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2- {4- [2-(3 -Bromo-phenyl)-ethy 1] -phenylamino} -benzoic acid; 2-{4-[2-(3-Fluoro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-methoxy-15 benzoic acid;<br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-nicotinic acid; 2~[2-(4-Fluoro-3-trifluoromethyl-phenyl)-2,3 -dihydro-1 H-isoindol-5-ylamino]-benzoic acid; or<br><br> 2- {4- [2-(3-Fluoro-4-methyl-phenyl)-ethyl] -phenylamino } -benzoic<br><br> 20 acid.<br><br> 23. The compounds:<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-pyrrol-1 -yl-25 benzoic acid;<br><br> 2-{4-[2-(4-Benzyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4-{2-[4-(3-Dimethylamino-propoxy)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Diethylamino-phenyl)-ethyl]-phenylamino}-benzoic<br><br> 30 acid;<br><br> 2- {4-[2-(4-Phenoxy-phenyl)-ethyl] -phenylamino } -benzoic acid; 2-{4-[2-(4-Octyloxy-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 00/76489 PCT/US00/15071<br><br> -127-<br><br> 2-(4- {2- [4-(2 -Ethoxy-1 -ethoxymethyl-ethyl)-phenyl] -ethyl} -phenylamino)-benzoic acid;<br><br> ■ 2-{4-[2-(4-Pyrrol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> or<br><br> 2-{4-[2-(4-Styryl-phenyl)-ethyl]-phenylamino}-benzoic acid.<br><br> The compoimds:<br><br> 2-{4-[2-(4-Dibutylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2- {4-[2-(4'-Ethyl-biphenyl -4-yl)-ethyl] -phenylamino } -benzoic acid;<br><br> 2-{4-[2-(4-Octyl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-(4- {2-[3-(3,5-Dichloro-phenoxy)-phenyl]-ethyl} -phenylamino)-benzoic acid;<br><br> 2-(4-{2-[4-(2-Chloro-6-fluoro-benzyloxy)-phenyl]-ethyl}-phenylamino)-benzoic acid;<br><br> 2-{4-[2-(4-Pyrazol-l-yl-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(4-Diphenylamino-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-(4- {2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethyl} -phenylamino)-benzoic acid;<br><br> 2- {4-[2-(3,4-Di chloro-phenyl)-ethyl]-phenylamino } -5-amino-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid;<br><br> 2- {4-[2-[(3,4-Di chl orophenyl)propyl]phenylamino } -5-nitrobenzoic acid;<br><br> 2-{4-[2-(3,4-Dimethyl-phenyl)-ethyl] phenylamino} -5-nitrobenzoic acid.<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -128-<br><br> 25. 2-[4-[2-(3,4-Dichlorophenyl)ethyl]phenyl]amino-benzoic acid or a pharmaceutically acceptable salt thereof.<br><br> 26. 2- {4- [3 -(3,4-Dichlorophenyl)propyl]phenylamino } benzoic acid or a pharmaceutically acceptable salt thereof.<br><br> 5 27. A compound which is selected from:<br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-5-nitro-benzoic acid;<br><br> 4-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-benzoic acid;<br><br> 10 4- {4- [3-(4-Diethylamino-phenyl)-propyl] -phenylamino } -3-<br><br> methoxy-benzoic acid;<br><br> 2-{4-[2-(3-Chloro-4-methyl-phenyl)-ethyI]-phenylamino}-5-methoxy-benzoic acid;<br><br> {4-[2-(3-Chloro-4-methyl-phenyl)-ethyl]-phenyl}-(2-methoxy-5-<br><br> 15 nitro-phenyl)-amine;<br><br> 2-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-3-nitro-benzoic acid;<br><br> 3-{4-[3-(4-Diethylamino-phenyl)-propyl]-phenylamino}-benzoic acid;<br><br> 20 2- {4-[2-(3,4-Dimethoxy-phenyl)-ethyl] -phenylamino } -benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid monosodium;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyI]-phenylamino}-benzoic acid<br><br> 25 monopotassium;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid calcium salt (1:1);<br><br> 2- {4-[2-(3,4-Di chl oro-phenyl)-ethyl] -phenylamino } -benzoate-2-hydroxy-1,1 -bis-hydroxymethyl-ethyl-ammonium;<br><br> 30 2-{4-[4-(3,4-Dichloro-phenyl)-butyl]-phenylamino}-5-methoxy-<br><br> benzoic acid;<br><br> 00/76489<br><br> PCT/US00/15071<br><br> -129-<br><br> 2- {4- [2-(3,4-Difluoro-phenyl)-ethyl]-phenylamiQO} -benzoic acid; 2-{3-[2-(4-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{3-[2-(3,4-Dimethyl-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(2,4-Dimethoxy-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(2-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(2-Hydroxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(3-Chloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2- [4-(2-Biphenyl~4-yl-ethyl)-phenylamino]-benzoic acid;<br><br> 2-{4-[2-(2,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 3-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid;<br><br> 4-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[2-(3,4,5-Trimethoxy-phenyl)-ethyl]-phenylarnino}-benzoic acid;<br><br> 2-{4-[2-(4-Phenoxy-phenyl)-ethyl]-phenylamino}-benzoic acid; 2-{4-[5-(3,4-Dichloro-phenyl)-pentyl]-phenylamino}-benzoic acid;<br><br> 4- {4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino } -2-methoxy-5-nitro-benzoic acid;<br><br> 2-{4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino }-5-fluoro-benzoic acid;<br><br> 5-Amino-2-{4-[5-(3,4-dichloro-phenyl)-pentyl]-phenylamino}-benzoic acid;<br><br> N-(2- {4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino}-benzoyl)-C,C,C-trifluoro-methanesulfonamide;<br><br> N-(2-{4-[3-(3,4-Dichloro-phenyl)-propyl]-phenylamino}-benzoyl)~ benzenesulfonamide;<br><br> 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-trifluoromethyl-benzoic acid;<br><br> 4-{4-[2-(3,4-Dichioro-phenyl)-ethyl]-phenylamino}risophthalic acid;<br><br> 00/76489<br><br> PCT/USOO/15071<br><br> -130-<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl3-phenylamiiio}-4-trifluoromethyl-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-3-trifiuoromethyl-benzoic acid;<br><br> 2-( {4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenyl} -methyl-amino)-5-. dimethylamino-benzoic acid;<br><br> 2 -({4-[2-(3,4-Di chloro-phenyI)-ethyl]-ph enyl} -methyl-amino)-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-dipropylamino-benzoic acid;<br><br> 5-Dibutylamino-2-{4-[2-(3,4-dichloro-phenyl)-ethyI]-phenylamino}-benzoic acid;<br><br> 2-{4-[2-(3,4-Dichloro-phenyl)-ethyl]-phenylamino}-5-diethylamino^beiizoic.acid;_<br><br> 4-[3-[4-{Diethylamino)phenyI]propyI]-N-(2-inethoxy-5-nitrophenyl)-benzinamine.<br><br> A method of imaging amyloid deposits, the method comprising: a. introducing a detectable quantity of a labeled compound having the Formula I or a pharmaceutically acceptable salt thereof into a patient by non-surgical means<br><br> ■N'<br><br> rs i<br><br> R R6<br><br> I<br><br> wherein<br><br> O<br><br> I<br><br> Ra is hydrogen, Cj-Cg alkyl, or -CC]-Cg alkyl; n is 1 to 5 inclusive;<br><br> WO 00/76489 PCT/US00/15071<br><br> -131-<br><br> r1, R2, r3, r4? r5? r7 ^ independently hydrogen, halogen,<br><br> -OH, -NH2, NRbRc, -C02H, -CO2C1-C6 alkyl, -N02, -OC^C^ alkyl, -Cj-Cg alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyl, -O-phenyl, -O-substituted phenyl, i O O<br><br> R 0<br><br> -CH=CH-phenyl, -0(CH2)pNRbRC, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C j -C6alkyl)(CH2)pNRbRc,<br><br> /CH2OC1-C6 alkyl<br><br> —CH \<br><br> CH2OCrC6 alkyl<br><br> 10 R8 is COOH, tetrazolyl, -S02Rd, or -C0NHS02Rd;<br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m-phenyl, or<br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-Cj-Cg alkylpiperazinyl, morpholino, 15 thiomorpholino, decahydroisoquinoline, or pyrazolyl;<br><br> Rd is hydrogen, -C^-Cg alkyl, -CF3, or phenyl;<br><br> m is 0 to 5 inclusive;<br><br> p is 1 to 5 inclusive;<br><br> AisCHorN;<br><br> 20 Rl and R2, when adjacent to one another, can be methylene-dioxy;<br><br> or the pharmaceutically acceptable salts thereof.<br><br> b. allowing sufficient time for the labeled compound to become associated with amyloid deposits; and c. detecting the labeled compound associated with the amyloid 25 deposits.<br><br> 29.<br><br> The method of Claim 28 wherein the patient has or is suspected to have Alzheimer's disease.<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -132-<br><br> 30. The method of Claim 28 wherein the labeled compound is a radio labeled compound.<br><br> 31. The method of Claim 28 wherein the labeled compound is detected using MRI.<br><br> 5 32. The compounds:<br><br> 2-[4-[2-(3,4-Dichlorophenyl)ethyl]phenyl]amino-benzoic acid; 2- {4-[2-(3,4-Dichloro-phenyl)-ethyl]phenylamino } -5-nitrobenzoic acid;<br><br> 2- (4-[3 -(3,4-Dichlorophenyl)-propyl]phenylamino } benzoic acid;<br><br> 10 2-[4-[2-(4-Chloro-3-trifluoromethylphenyl)ethyl]phenyl]amino-<br><br> benzoic acid; and<br><br> 2-{4-[3-(4-Diethylaminophenyl)propyI]phenylamino}benzoic acid.<br><br> 33. A pharmaceutical formulation comprising a compound of Claim 19 admixed with a pharmaceutically acceptable diluent, excipient, or carrier<br><br> 15 therefor.<br><br> 34. A pharmaceutical formulation comprising a compound of Claim 20 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 35. A pharmaceutical formulation comprising a compound of Claim 21<br><br> 20 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 36.<br><br> A pharmaceutical formulation comprising a compound of Claim 22 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> WO 00/76489<br><br> PCT/US00/15071<br><br> -133-<br><br> 37. A pharmaceutical formulation comprising a compound of Claim 23 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 38. A pharmaceutical formulation comprising a compound of Claim 24<br><br> 5 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 39. A pharmaceutical formulation comprising a compound of Claim 25 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 10 40. A pharmaceutical formulation comprising a compound of Claim 26<br><br> admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefon<br><br> 15<br><br> 41. A pharmaceutical formulation comprising a compound of Claim 32<br><br> admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> 42. A compound of Formula 1.<br><br> R"<br><br> R<br><br> RJ<br><br> =h<br><br> R<br><br> R-<br><br> 20<br><br> wherein<br><br> O<br><br> Ra is hydrogen, C^-Cg alkyl, or -CC]-Cg alkyl; j.<br><br> n is 1 to 5 inclusive;<br><br> Rl, R2, Rj, R^, R^, r6; and R~ are independently hydrogen, halogen,<br><br> -OH, -NH2, NRbRc, -C02H, -C02Ci-C6 alkyl, -N02, -OC]-C12<br><br> 89 PCTAJSOO/15071<br><br> -134-<br><br> alkyl, -C]-Cg alkyl, -CF3, -CN, -OCH2 phenyl, -OCH2-substituted phenyl, -(CH2)m-phenyl, -O-phenyl, -O-substituted phenyl,<br><br> 0 O<br><br> 1 II<br><br> -CH=CH-phenyl, -0(CH2)pNRbRc, -CNRbRc, -NHCRb, -NH(CH2)pNRbRc, -N(C ] -C6alkyl)(CH2)pNRbRc,<br><br> /C^OCj-Cg alkyl<br><br> —CH \<br><br> CH20CrC6 alkyl<br><br> R8 is COOH, tetrazolyl, -S02Rd or -C0NHS02Rd;<br><br> Rb and Rc are independently hydrogen, -Cj-Cg alkyl, -(CH2)m-phenyl, or<br><br> Rb and Rc taken together with the nitrogen atom to which they are attached form a cyclic ring selected from piperidinyl, pyrrolyl, imidazolyl, piperazinyl, 4-Ci-Cg alkylpiperazinyl, morpholino, thiomoipholino, decahydroisoquinoline, or pyrazolyl;<br><br> Rd is hydrogen, -Cj-Cg alkyl, -CF3, or phenyl;<br><br> m is 0 to 5 inclusive;<br><br> p is 1 to 5 inclusive;<br><br> AisCHorN;<br><br> Rl and R2, when adjacent to one another, can be methylene-dioxy;<br><br> or the pharmaceutically acceptable salts thereof.<br><br> A pharmaceutical formulation comprising a compound of Claim 42 admixed with a pharmaceutically acceptable diluent, excipient, or carrier therefor.<br><br> -135 -<br><br> 44. The use of Claim 1 substantially as herein described with reference to any one of Examples 1 to 163.<br><br> 45. The use of Claim 10 substantially as herein described with reference to any one of Examples 1 to 163.<br><br> 46. The use of Claim 17 substantially as herein described with reference to any one of Examples 1 to 163.<br><br> 47. A compound according to any one of Claims 19 to 27 or Claim 32 as specifically set forth herein.<br><br> 48. The method of Claim 28 substantially as herein described with reference to any one of Examples 1 to 163.<br><br> 49. A pharmaceutical formulation of any one of Claims 33 to 41 substantially as herein described with reference to any one of Examples 1 to 163.<br><br> 50. A compound of Claim 42 as specifically set forth herein.<br><br> </p> </div>
NZ515621A 1999-06-10 2000-05-31 Medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits NZ515621A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13855099P 1999-06-10 1999-06-10
PCT/US2000/015071 WO2000076489A2 (en) 1999-06-10 2000-05-31 Method of inhibiting amyloid protein aggregation and imaging amyloid deposits

Publications (1)

Publication Number Publication Date
NZ515621A true NZ515621A (en) 2004-05-28

Family

ID=22482537

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ515621A NZ515621A (en) 1999-06-10 2000-05-31 Medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits

Country Status (30)

Country Link
EP (1) EP1225886A2 (en)
JP (1) JP2003504310A (en)
KR (1) KR20020008224A (en)
CN (1) CN1378446A (en)
AP (1) AP2002002387A0 (en)
AU (1) AU775157B2 (en)
BG (1) BG106293A (en)
BR (1) BR0011728A (en)
CA (1) CA2375551A1 (en)
CR (1) CR6528A (en)
DZ (1) DZ3252A1 (en)
EA (1) EA004632B1 (en)
EE (1) EE200100673A (en)
GE (1) GEP20053423B (en)
HK (1) HK1048258A1 (en)
HR (1) HRP20020026A2 (en)
HU (1) HUP0202508A3 (en)
IL (1) IL146971A0 (en)
IS (1) IS6193A (en)
MA (1) MA26805A1 (en)
MX (1) MXPA01012318A (en)
NO (1) NO20015995L (en)
NZ (1) NZ515621A (en)
OA (1) OA11963A (en)
PL (1) PL352430A1 (en)
SK (1) SK17632001A3 (en)
TR (1) TR200103551T2 (en)
WO (1) WO2000076489A2 (en)
YU (1) YU86701A (en)
ZA (1) ZA200109794B (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030138374A1 (en) * 2000-03-22 2003-07-24 Yukitsuda Kudo Image diagnosis probe based on substituted azobenzene or analogue thereof for disease attributable to amyloid accumulation and composition for image diagnosis containing the same
CA2357450A1 (en) * 2000-09-29 2002-03-29 Warner-Lambert Company Phenoxazine analogs useful as amyloid aggregation inhibitors and treatment of alzheimer's disease and disorders related to amyloidosis
GB0225548D0 (en) 2002-11-01 2002-12-11 Glaxo Group Ltd Compounds
ES2319596B1 (en) 2006-12-22 2010-02-08 Laboratorios Almirall S.A. NEW DERIVATIVES OF THE AMINO-NICOTINIC AND AMINO-ISONICOTINIC ACIDS.
ES2327372B1 (en) * 2007-04-23 2010-08-24 Laboratorios Almirall S.A. NEW DERIVATIVES OF THE AMINO-NICOTINIC AND AMINO-ISONICOTINIC ACIDS.
EP2121633A2 (en) 2007-02-12 2009-11-25 Merck & Co., Inc. Piperazine derivatives for treatment of ad and related conditions
US20080253967A1 (en) * 2007-04-13 2008-10-16 Kung Hank F Halo-Stilbene Derivatives And Their Use For Binding And Imaging Of Amyloid Plaques
UY31272A1 (en) 2007-08-10 2009-01-30 Almirall Lab NEW DERIVATIVES OF AZABIFENILAMINOBENZOIC ACID
EP2135610A1 (en) 2008-06-20 2009-12-23 Laboratorios Almirall, S.A. Combination comprising DHODH inhibitors and methotrexate
CA2735158C (en) 2008-08-29 2016-11-08 Treventis Corporation Compositions and methods of treating amyloid disease
EP2239256A1 (en) 2009-03-13 2010-10-13 Almirall, S.A. Sodium salt of 5-cyclopropyl-2-{[2-(2,6-difluorophenyl)pyrimidin-5-yl]amino}benzoic acid as DHODH inhibitor
EP2228367A1 (en) * 2009-03-13 2010-09-15 Almirall, S.A. Addition salts of amines containing hydroxyl and/or carboxylic groups with amino nicotinic acid derivatives as DHODH inhibitors
EP2314577A1 (en) 2009-10-16 2011-04-27 Almirall, S.A. Process for manufacturing 2-[(3,5-difluoro-3'-methoxy-1,1'-biphenyl-4-yl)amino]nicotinic acid
EP2536405A1 (en) * 2010-02-16 2012-12-26 Universita Degli Studi di Siena Non peptidic 14-3-3 inhibitors and the use thereof
WO2012071186A1 (en) * 2010-11-24 2012-05-31 Allergan, Inc. Modulators of s1p receptors
WO2018157843A1 (en) * 2017-03-02 2018-09-07 中国科学院上海药物研究所 2-(substituted benzene matrix) aromatic formate fto inhibitor, preparation method therefor, and applications thereof
CN111183129B (en) * 2017-08-07 2024-07-23 国立大学法人广岛大学 Novel anthranilic acid compound, pin1 inhibitor using same, and therapeutic agent for inflammatory disease and cancer

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5196444A (en) * 1990-04-27 1993-03-23 Takeda Chemical Industries, Ltd. 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof
US5739169A (en) * 1996-05-31 1998-04-14 Procept, Incorporated Aromatic compounds for inhibiting immune response
SK17622001A3 (en) * 1999-06-10 2003-06-03 Warner-Lambert Company Method of inhibiting amyloid protein aggregation and imaging amyloid deposits using isoindoline derivatives

Also Published As

Publication number Publication date
KR20020008224A (en) 2002-01-29
HUP0202508A2 (en) 2002-12-28
GEP20053423B (en) 2005-01-25
NO20015995D0 (en) 2001-12-07
AP2002002387A0 (en) 2002-03-31
IS6193A (en) 2001-12-07
CN1378446A (en) 2002-11-06
MA26805A1 (en) 2004-12-20
YU86701A (en) 2004-09-03
CA2375551A1 (en) 2000-12-21
JP2003504310A (en) 2003-02-04
WO2000076489A2 (en) 2000-12-21
PL352430A1 (en) 2003-08-25
SK17632001A3 (en) 2003-03-04
AU5455300A (en) 2001-01-02
HK1048258A1 (en) 2003-03-28
IL146971A0 (en) 2002-08-14
WO2000076489A3 (en) 2002-05-30
AU775157B2 (en) 2004-07-22
HRP20020026A2 (en) 2003-08-31
BG106293A (en) 2002-06-28
EP1225886A2 (en) 2002-07-31
EE200100673A (en) 2003-02-17
EA004632B1 (en) 2004-06-24
DZ3252A1 (en) 2000-12-21
HUP0202508A3 (en) 2003-03-28
OA11963A (en) 2006-04-17
CR6528A (en) 2004-02-23
ZA200109794B (en) 2003-07-01
TR200103551T2 (en) 2002-12-23
MXPA01012318A (en) 2002-07-22
EA200101135A1 (en) 2002-06-27
NO20015995L (en) 2002-02-04
BR0011728A (en) 2002-02-26

Similar Documents

Publication Publication Date Title
NZ515621A (en) Medicaments for inhibiting amyloid protein aggregation and methods of imaging amyloid deposits
EP1192131B1 (en) Method of inhibiting amyloid protein aggregation and imaging amyloid deposits using isoindoline derivatives
US6001331A (en) Method of imaging amyloid deposits
US6972287B1 (en) Method of inhibiting amyloid protein aggregation and imaging amyloid deposits
US4086272A (en) Phenyl-alkanolamine, alkylamine and alpha-aminoalkyl ketone derivatives as heart stimulants
EP1284958A1 (en) Method of inhibiting amyloid protein aggregation and imaging amyloid deposits using aminoidane derivatives
US4137328A (en) Phenyl-alkanolamine, alkylamine and α-aminoalkyl ketone derivatives as heart stimulants
DE69600272T2 (en) Quinoline-4-carbonylguanidine derivatives, processes for their preparation and pharmaceutical compositions containing them
JPS60112778A (en) Morpholine derivatives, manufacture and medicinal composition
JP2003502321A (en) Rhodanin derivatives and their use in amyloid inhibition and imaging
CA2374616A1 (en) Rhodanine derivatives for use in a method of inhibiting amyloid protein aggregation and imaging amyloid deposits
EP1193260B1 (en) Phenoxazine analogs for the treatment of amyloidosis
GB2162523A (en) Intermediates for syntheses of indole derivatives
JPH0657687B2 (en) Fluorodinitrobenzene derivative and method for producing the same

Legal Events

Date Code Title Description
RENW Renewal (renewal fees accepted)
PSEA Patent sealed
ASS Change of ownership

Owner name: WARNER-LAMBERT COMPANY, US

Free format text: OLD OWNER(S): WARNER-LAMBERT COMPANY; YAMANOUCHI PHARMACEUTICAL CO, LTD