TRPV1 ANTAGONISTS INCLUDING DIHYDROXY SUBSTITUENT AND USES THEREOF

1. FIELD

The disclosure relates to Compounds of Formula (I), and pharmaceutically acceptable derivatives thereof, compositions comprising an effective amount of a Compound of Formula (I) and methods for treating or preventing a condition such as pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, and IBS, comprising administering to an animal in need thereof an effective amount of a Compound of Formula (I).

2. BACKGROUND

Pain is the most common symptom for which patients seek medical advice and treatment. Pain can be acute or chronic. While acute pain is usually self-limited, chronic pain persists for three months or longer and can lead to significant changes in a patient's personality, lifestyle, functional ability and overall quality of life (Foley, “Pain,” in Cecil Textbook of Medicine, pp. 100-107 (Bennett and Plum eds., 20th ed. 1996)).

Moreover, chronic pain can be classified as either nociceptive or neuropathic. Nociceptive pain includes tissue injury-induced pain and inflammatory pain such as that associated with arthritis.

Neuropathic pain is caused by damage to the peripheral or central nervous system and is maintained by aberrant somatosensory processing. There is a large body of evidence relating activity at vanilloid receptors (Di Marzo et al., “Endovanilloid signaling in pain,” Current Opinion in Neurobiology 12:372-379 (2002)) to pain processing.

Nociceptive pain has been traditionally managed by administering non-opioid analgesics, such as acetylsalicylic acid, choline magnesium trisalicylate, acetaminophen, ibuprofen, fenoprofen, diflusinal, and naproxen; or opioid analgesics, including morphine, hydromorphone, methadone, levorphanol, fentanyl, oxycodone, and oxymorphone. Id. In addition to the above-listed treatments, neuropathic pain, which can be difficult to treat, has also been treated with anti-epileptics (e.g., gabapentin, carbamazepine, valproic acid, topiramate, phenytoin), NMDA antagonists (e.g., ketamine, dextromethorphan), topical lidocaine (for post-herpetic neuralgia), and tricyclic antidepressants (e.g., fluoxetine, sertraline and amitriptyline).

UI is uncontrollable urination, generally caused by bladder-detrusor-muscle instability. UI affects people of all ages and levels of physical health, both in health care settings and in the community at large. Physiologic bladder contraction results in large part from acetylcholine-induced stimulation of post-ganglionic muscarinic-receptor sites on bladder smooth muscle. Treatments for UI include the administration of drugs having bladder-relaxant properties, which help to control bladder-detrusor-muscle overactivity.

None of the existing commercial drug treatments for UI has achieved complete success in all classes of UI patients, nor has treatment occurred without significant adverse side effects.

Treatment of ulcers often involves reducing or inhibiting the aggressive factors. For example, antacids such as aluminum hydroxide, magnesium hydroxide, sodium bicarbonate, and calcium bicarbonate can be used to neutralize stomach acids. Antacids, however, can cause alkalosis, leading to nausea, headache, and weakness. Antacids can also interfere with the absorption of other drugs into the blood stream and cause diarrhea.

H₂antagonists, such as cimetidine, ranitidine, famotidine, and nizatidine, are also used to treat ulcers. H₂antagonists promote ulcer healing by reducing gastric acid and digestive-enzyme secretion elicited by histamine and other H₂agonists in the stomach and duodenum. H₂antagonists, however, can cause breast enlargement and impotence in men, mental changes (especially in the elderly), headache, dizziness, nausea, myalgia, diarrhea, rash, and fever.

H⁺, K⁺-ATPase inhibitors such as omeprazole and lansoprazole are also used to treat ulcers. H⁺, K⁺-ATPase inhibitors inhibit the production of enzymes used by the stomach to secrete acid. Side effects associated with H⁺, K⁺-ATPase inhibitors include nausea, diarrhea, abdominal colic, headache, dizziness, somnolence, skin rashes, and transient elevations of plasma activities of aminotransferases.

Inflammatory-bowel disease (“IBD”) is a chronic disorder in which the bowel becomes inflamed, often causing recurring abdominal cramps and diarrhea. The two types of IBD are Crohn's disease and ulcerative colitis.

Crohn's disease, which can include regional enteritis, granulomatous ileitis, and ileocolitis, is a chronic inflammation of the intestinal wall. Crohn's disease occurs equally in both sexes and is more common in Jews of eastern-European ancestry. Most cases of Crohn's disease begin before age 30 and the majority start between the ages of 14 and 24. The disease often affects the full thickness of the intestinal wall. Generally the disease affects the lowest portion of the small intestine (ileum) and the large intestine, but can occur in any part of the digestive tract.

Cramps and diarrhea, side effects associated with Crohn's disease, can be relieved by anticholinergic drugs, diphenoxylate, loperamide, deodorized opium tincture, or codeine.

When Crohn's disease causes the intestine to be obstructed or when abscesses or fistulas do not heal, surgery can be necessary to remove diseased sections of the intestine. Surgery, however, does not cure the disease, and inflammation tends to recur where the intestine is rejoined. In almost half of the cases a second operation is needed. Berkow et al., eds., “Crohn's Disease,” Merck Manual of Medical Information, pp. 528-530 (1997).

Ulcerative colitis is a chronic disease in which the large intestine becomes inflamed and ulcerated, leading to episodes of bloody diarrhea, abdominal cramps, and fever. Ulcerative colitis usually begins between ages 15 and 30; however, a small group of people have their first attack between ages 50 and 70. Unlike Crohn's disease, ulcerative colitis never affects the small intestine and does not affect the full thickness of the intestine. The disease usually begins in the rectum and the sigmoid colon and eventually spreads partially or completely throughout the large intestine. The cause of ulcerative colitis is unknown.

Treatment of ulcerative colitis is directed to controlling inflammation, reducing symptoms, and replacing lost fluids and nutrients. Anticholinergic drugs and low doses of diphenoxylate or loperamide are administered for treating mild diarrhea. For more intense diarrhea higher doses of diphenoxylate or loperamide, or deodorized opium tincture or codeine are administered.

Irritable-bowel syndrome (“IBS”) is a disorder of motility of the entire gastrointestinal tract, causing abdominal pain, constipation, and/or diarrhea. IBS affects three-times more women than men. In IBS, stimuli such as stress, diet, drugs, hormones, or irritants can cause the gastrointestinal tract to contract abnormally. During an episode of IBS, contractions of the gastrointestinal tract become stronger and more frequent, resulting in the rapid transit of food and feces through the small intestine, often leading to diarrhea. Cramps result from the strong contractions of the large intestine and increased sensitivity of pain receptors in the large intestine.

Treatment of IBS often involves modification of an IBS-patient's diet. Often it is recommended that an IBS patient avoid beans, cabbage, sorbitol, and fructose. A low-fat, high-fiber diet can also help some IBS patients. Regular physical activity can also help keep the gastrointestinal tract functioning properly. Drugs such as propantheline that slow the function of the gastrointestinal tract are generally not effective for treating IBS. Antidiarrheal drugs, such as diphenoxylate and loperamide, help with diarrhea. Berkow et al., eds., “Irritable Bowel Syndrome,” Merck Manual of Medical Information, pp. 525-526 (1997).

International publication no. WO 98/31677 describes a class of aromatic amines derived from cyclic amines that are useful as antidepressant drugs. International publication no. WO 01/027107 describes a class of heterocyclic compounds that are sodium/proton exchange inhibitors. International publication no. WO 99/37304 describes substituted oxoazaheterocyclic compounds useful for inhibiting factor Xa. U.S. Pat. No. 6,248,756 to Anthony et al. and international publication no. WO 97/38665 describe a class of piperidine-containing compounds that inhibit farnesyl-protein transferase (Ftase). International publication no. WO 98/31669 describes a class of aromatic amines derived from cyclic amines useful as antidepressant drugs. International publication no. WO 97/28140 describes a class of piperidines derived from 1-(piperazin-1-yl)aryl(oxy/amino)carbonyl-4-aryl-piperidine that are useful as 5-HT_1Dbreceptor antagonists. International publication no. WO 97/38665 describes a class of piperidine containing compounds that are useful as inhibitors of farnesyl-protein transferase.

U.S. Pat. No. 4,797,419 to Moos et al. describes a class of urea compounds for stimulating the release of acetylcholine and useful for treating symptoms of senile cognitive decline. U.S. Pat. No. 5,891,889 to Anthony et al. describes a class of substituted piperidine compounds that are useful as inhibitors of farnesyl-protein transferase, and the farnesylation of the oncogene protein Ras. U.S. Pat. No. 6,150,129 to Cook et al. describes a class of dinitrogen heterocycles useful as antibiotics. U.S. Pat. No. 5,529,998 to Habich et al. describes a class of benzooxazolyl- and benzothiazolyloxazolidones useful as antibacterials.

International publication no. WO 01/57008 describes a class of 2-benzothiazolyl urea derivatives useful as inhibitors of serine/threonine and tyrosine kinases. International publication no. WO 02/08221 describes aryl piperazine compounds useful for treating chronic and acute pain conditions, itch, and urinary incontinence. International publication no. WO 00/59510 describes aminopyrimidines useful as sorbitol dehydrogenase inhibitors.

Japanese patent application no. 11-199573 to Kiyoshi et al. describes benzothiazole derivatives that are neuronal 5HT3 receptor agonists in the intestinal canal nervous system and useful for treating digestive disorders and pancreatic insufficiency. German patent application no 199 34 799 to Rainer et al. describes a chiral-smectic liquid crystal mixture containing compounds with 2 linked (hetero)aromatic rings or compounds with 3 linked (hetero)aromatic rings.

Chu-Moyer et al., J. Med. Chem. 45:511-528 (2002) describes heterocycle-substituted piperazino-pyrimidines useful as sorbitol dehydrogenase inhibitors. Khadse et al., Bull. Haff. Instt. 1(3):27-32 (1975) describes 2-(N⁴-substituted-N¹-piperazinyl) pyrido(3,2-d)thiazoles and 5-nitro-2-(N⁴-substituted-N¹-piperazinyl)benzthiazoles useful as anthelmintic agents.

U.S. Patent Application Publication No. US 2004/0186111 A1 and International publication no. WO 2004/058754 A1 describe a class of compounds that are useful for treating pain. U.S. Patent Application Publication No. US 2006/0199824 A1 and International publication no. WO 2005/009987 A1 describe a class of compounds that are useful for treating pain. U.S. Patent Application Publication No. US 2006/0128717 A1 and International publication no. WO 2005/009988 A1 describe a class of compounds that are useful for treating pain. U.S. Patent Application Publication Nos. US 2009/0170867 A1, US 2009/0170868 A1, and 2009/0176796 A1 and International publication no. WO 2008/132600 A2 describe a class of compounds that are useful for treating pain.

There remains, however, a clear need in the art for new drugs useful for treating or preventing pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, and IBS. Citation of any reference in Section 2 of this application is not to be construed as an admission that such reference is prior art to the present application.

3. SUMMARY

In a first aspect of the disclosure, new compounds that exhibit affinity for the TRPV1 receptor are described.

In some embodiments, such new compounds exhibit antagonist activity at the TRPV1 receptor. In other embodiments, such new compounds exhibit partial antagonist activity at the TRPV1 receptor.

Certain new compounds of the disclosure can be used to treat an animal suffering from pain, e.g., chronic or acute pain.

In another aspect of the disclosure, methods of treating chronic or acute pain in an animal by administering one or more Compounds of Formula (I) to an animal in need of such treatment are described. In certain embodiments, such new Compounds of Formula (I) effectively treat chronic or acute pain in the animal, while producing fewer or reduced side effects compared to previously available compounds.

Compounds of Formula (I) are herein disclosed:

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or a pharmaceutically acceptable derivative thereof, where:

R₁is -halo or —CF₃;

R₄is —H or —CH₃;

each R₈and R₉is independently —H, -halo, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OR₁₀;

R₁₀is —(C₁-C₄)alkyl;

- each halo is independently —F, —Cl, —Br, or —I; and

m is the integer 0 or 1;

(1) provided that if R₄is —H then m is 1; and

(2) provided that if R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

In another embodiment in connection with a Compound of Formula (I), it is further provided that:

(4) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —F, and R₉is —F, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group or a (S)-3-methyl group; and/or

(5) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, R₉is -halo, and m is 1, then the methyl group bonded to the piperazine ring is a (S)-3-methyl group or a (R)-3-methyl group.

Compounds of Formula (I) are potent at TRPV1 receptors, and are soluble in aqueous solutions at either pH 6.8 or pH 1.2.

A Compound of Formula (I), or a pharmaceutically acceptable derivative thereof, is useful for treating or preventing pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS (each being a “Condition”) in an animal.

The disclosure also relates to compositions comprising an effective amount of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof, and a pharmaceutically acceptable carrier or excipient. The compositions are useful for treating or preventing a Condition in an animal.

The disclosure further relates to methods for treating a Condition comprising administering to an animal in need thereof an effective amount of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof.

The disclosure further relates to a Compound of Formula (I), a pharmaceutically acceptable derivative thereof, a composition containing a Compound of Formula (I), and/or a composition containing a pharmaceutically acceptable derivative of a Compound of Formula (I) for use in the treatment of pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal.

The disclosure further relates to use of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof, in the manufacture of a medicament for treating and/or preventing a Condition, such as pain and/or osteoarthritis. The disclosure further relates to a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof, for use in the treatment and/or prevention of a Condition, such as pain and/or osteoarthritis.

The disclosure further relates to methods for preventing a Condition comprising administering to an animal in need thereof an effective amount of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof.

The disclosure still further relates to methods for inhibiting Transient Receptor Potential Vanilloid 1 (“TRPV1,” formerly known as Vanilloid Receptor 1 or VR1) function in a cell, comprising contacting a cell capable of expressing TRPV1 with an effective amount of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof.

The disclosure still further relates to a method for preparing a composition comprising the step of admixing a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof, and a pharmaceutically acceptable carrier or excipient.

The disclosure still further relates to a kit comprising a container containing an effective amount of a Compound of Formula (I), or a pharmaceutically acceptable derivative thereof.

In one embodiment, preferred Compounds of Formula (I) are Compounds of Formula (II):

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or a pharmaceutically acceptable derivative thereof, where:

R₄is —H or —CH₃;

R₈is —H, —F, or —CH₃;

R₉is —H, -halo, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃; and

each halo is independently —F, —Cl, —Br, or —I;

(1) provided that if R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

In another embodiment in connection with a Compound of Formula (II), it is further provided that:

(2) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group;

(3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —F, and R₉is —F, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group or a (S)-3-methyl group; and/or

(4) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (S)-3-methyl group or a (R)-3-methyl group.

Many Compounds of Formula (II) are soluble, in some cases highly soluble, in aqueous solutions at either pH 6.8 or pH 1.2, are potent at TRPV1 receptors, are orally bioavailable, have a good therapeutic index, and are believed to be highly efficacious in animals for the treatment of pain and/or osteoarthritis. Moreover, Compounds of Formula (II) are capable of ameliorating undesirable side effects, such as an increase in body temperature that can occur upon in vivo administration of some compounds which modulate the TRPV1 receptor.

The disclosure can be understood more fully by reference to the following detailed description and illustrative examples, which are intended to exemplify non-limiting embodiments of the disclosure.

3.1. BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the PXRD pattern (CuKα radiation) of the product prepared with Compound A155(a) and fumaric acid.

FIG. 2 depicts ¹⁵N NMR CP/MAS spectra of the product prepared with Compound A155(a) and fumaric acid, the dihydrochloride-salt of Compound A155(a) and the free base of Compound A155(a).

FIG. 3 depicts the ¹³C NMR CP/MAS spectrum of the product prepared with Compound A155(a) and fumaric acid.

4. DETAILED DESCRIPTION

The invention includes the following:

(1.) A Compound of Formula (I):

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or a pharmaceutically acceptable derivative thereof, wherein:

R₁is -halo or —CF₃;

R₄is —H or —CH₃;

each R₈and R₉is independently —H, -halo, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OR₁₀;

R₁₀is —(C₁-C₄)alkyl;

each halo is independently —F, —Cl, —Br, or —I; and m is the integer 0 or 1;

- (1) provided that if R₄is —H then m is 1; and
- (2) provided that if R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

(2.) The compound of the above (1.) or a pharmaceutically acceptable derivative thereof, wherein it is further provided that:

- (3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group;
- (4) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —F, and R₉is —F, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group or a (S)-3-methyl group; and/or
- (5) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, R₉is -halo, and m is 1, then the methyl group bonded to the piperazine ring is a (S)-3-methyl group or a (R)-3-methyl group.

(3.) The compound of the above (1.) or (2.) or a pharmaceutically acceptable derivative thereof, wherein R₁is —F, —Cl, or —CF₃.

(4.) The compound of any one of the above (1.) to (3.) or a pharmaceutically acceptable derivative thereof, wherein R₁is —F.

(5.) The compound of any one of the above (1.) to (4.) or a pharmaceutically acceptable derivative thereof, wherein R₁₀is —CH₃or —CH₂CH₃.

(6.) The compound of any one of the above (1.) to (5.) or a pharmaceutically acceptable derivative thereof, wherein R₁₀is —CH₂CH₃.

(7.) The compound of any one of the above (1.) to (6.) or a pharmaceutically acceptable derivative thereof, wherein R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃.

(8.) The compound of any one of the above (1.) to (7.) or a pharmaceutically acceptable derivative thereof, wherein R₈is —H, —F, or —CH₃.

(9.) The compound of any one of the above (1.) to (8.) or a pharmaceutically acceptable derivative thereof, wherein R₈is —F or —CH₃.

(10.) The compound of any one of the above (1.) to (9.) or a pharmaceutically acceptable derivative thereof, wherein R₉is —H.

(11.) The compound of any one of the above (1.) to (10.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

(12.) The compound of any one of the above (1.) to (10.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

(13.) The compound of any one of the above (1.) to (10.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration.

(14.) The compound of any one of the above (1.) to (10.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —H and the carbon atom at the a position of the a-b bond is in the (R) configuration.

(15.) The compound of any one of the above (1.) to (14.) or a pharmaceutically acceptable derivative thereof, wherein m is 1 and the methyl group bonded to the piperazine ring is a (S)-2-methyl group.

(16.) The compound of the above (1.) to (15.), wherein the pharmaceutically acceptable derivative is a pharmaceutically acceptable salt, radiolabeled form, a co-crystal, or a combination thereof.

(17.) The compound of the above (15.) or (16.), wherein the pharmaceutically acceptable derivative is a hydrochloride salt, a sodium salt, a potassium salt, a p-toluenesulfonic acid salt, a fumaric acid-salt, or a fumarate co-crystal.

(18.) The compound of any one of the above (15.) to (16.), wherein the pharmaceutically acceptable derivative is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(19.) The compound of any one of the above (1.) to (12.) or a pharmaceutically acceptable derivative thereof, wherein m is 0.

(20.) The compound of the above (19.), wherein the pharmaceutically acceptable derivative is a pharmaceutically acceptable salt, radiolabeled form, or a hydrochlorate, tartrate, benzenesulfonate, p-toluenesulfonate, or fumarate co-crystal.

(21.) The compound of the above (19.) or (20.), wherein the pharmaceutically acceptable derivative is a hydrochloride salt, a sodium salt, a potassium salt, a p-toluenesulfonic acid salt, a fumaric acid-salt, or a fumarate co-crystal.

(22.) The compound of the above (19.), wherein the pharmaceutically acceptable derivative is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(23.) The compound of any one of the above (1.) to (8.), (11.), or (19.) or a pharmaceutically acceptable derivative thereof, which is

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(24.) The compound of any one of the above (1.) to (3.), (5.) to (8.), (11.), or (19.) or a pharmaceutically acceptable derivative thereof, which is

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(25.) The compound of any one of the above (1.) to (8.), (11.), or (19.) or a pharmaceutically acceptable derivative thereof, which is

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(26.) The compound of any one of the above (1.) to (9.), (11.), or (19.) or a pharmaceutically acceptable derivative thereof, which is

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(27.) The compound of any one of the above (23.) to (26.), which is a free base.

(28.) The compound of any one of the above (23.) to (26.), which is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(29.) A composition comprising the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof and a pharmaceutically acceptable carrier or excipient.

(30.) A method for treating pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof.

(31.) A method for treating pain, pain associated with osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof.

(32.) A method for treating pain, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof.

(33.) A method for treating pain, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof.

(34.) A method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of the compound of any one of the above (1.) to (28.) or a pharmaceutically acceptable derivative thereof.

(35.) The product of combining the compound of any one of the above (1.) to (28.) with fumaric acid, where the molar ratio in the product is about 1:0.5 of (the Compound of Formula (I)):(fumaric acid).

(36.) A composition comprising the product of the above (35.) and a pharmaceutically acceptable carrier or excipient.

(37.) A method for treating pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (35.).

(38.) A method for treating pain, pain associated with osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (35.).

(39.) A method for treating pain, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (35.).

(40.) A method for treating pain, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (35.).

(41.) A method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of the product of the above (35.).

(42.) The compound of any one of the above (1.), (4.), (6.), or (8.), which is a compound of formula (II):

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or a pharmaceutically acceptable derivative thereof, wherein:

R₄is —H or —CH₃;

R₈is —H, —F, or —CH₃;

R₉is —H, -halo, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃; and

each halo is independently —F, —Cl, —Br, or —I;

- (1) provided that if R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

(43.) The compound of the above (42.) or a pharmaceutically acceptable derivative thereof, wherein it is further provided that:

- (2) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group;
- (3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —F, and R₉is —F, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group or a (S)-3-methyl group; and/or
- (4) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (S)-3-methyl group or a (R)-3-methyl group.

(44.) The compound of the above (42.) or (43.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

(45.) The compound of the above (42.) or (43.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

(46.) The compound of the above (42.) or (43.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration.

(47.) The compound of the above (42.) or (43.) or a pharmaceutically acceptable derivative thereof, wherein R₄is —H and the carbon atom at the a position of the a-b bond is in the (R) configuration.

(48.) The compound of any one of the above (42.) to (47.) or a pharmaceutically acceptable derivative thereof, wherein the methyl group bonded to the piperazine ring is a (S)-3-methyl group.

(49.) The compound of the above (48.) or a pharmaceutically acceptable derivative thereof, wherein R₉is —H.

(50.) The compound of the above (48.) or (49.) or a pharmaceutically acceptable derivative thereof, wherein R₈is —F.

(51.) The compound of any one of the above (48.) to (50.), wherein the pharmaceutically acceptable derivative is a pharmaceutically acceptable salt, or a fumarate co-crystal.

(52.) The compound of any one of the above (48.) to (51.), wherein the pharmaceutically acceptable derivative is a hydrochloride salt, a sodium salt, a potassium salt, a p-toluenesulfonic acid salt, a fumaric acid-salt, or a fumarate co-crystal.

(53.) The compound of any one of the above (48.) to (50.), wherein the pharmaceutically acceptable derivative is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(54.) The compound of any one of the above (42.) to (47.) or a pharmaceutically acceptable derivative thereof, wherein the methyl group bonded to the piperazine ring is a (S)-2-methyl group.

(55.) The compound of the above (54.) or a pharmaceutically acceptable derivative thereof, wherein R₉is —H.

(56.) The compound of the above (54.) or (55.) or a pharmaceutically acceptable derivative thereof, wherein R₈is —F.

(57.) The compound of any one of the above (54.) to (56.), wherein the pharmaceutically acceptable derivative is a pharmaceutically acceptable salt, or a fumarate co-crystal.

(58.) The compound of any one of the above (54.) to (57.), wherein the pharmaceutically acceptable derivative is a hydrochloride salt, a sodium salt, a potassium salt, a p-toluenesulfonic acid salt, a fumaric acid-salt, or a fumarate co-crystal.

(59.) The compound of any one of the above (54.) to (56.), wherein the pharmaceutically acceptable derivative is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(60.) The compound of any one of the above (42.) to (47.) or a pharmaceutically acceptable derivative thereof, wherein the methyl group bonded to the piperazine ring is a (R)-3-methyl group.

(61.) The compound of the above (60.) or a pharmaceutically acceptable derivative thereof, wherein R₉is —H.

(62.) The compound of the above (60.) or (61.) or a pharmaceutically acceptable derivative thereof, wherein R₈is —F.

(63.) The compound of any one of the above (60.) to (62.), wherein the pharmaceutically acceptable derivative is a pharmaceutically acceptable salt, or a fumarate co-crystal.

(64.) The compound of any one of the above (60.) to (63.), wherein the pharmaceutically acceptable derivative is a hydrochloride salt, a sodium salt, a potassium salt, a p-toluenesulfonic acid salt, a fumaric acid-salt, or a fumarate co-crystal.

(65.) The compound of any one of the above (60.) to (62.), wherein the pharmaceutically acceptable derivative is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(66.) The compound of any one of the above (42.), (43.), (46.), (54.), (55.), or (57.) to (59.) or a pharmaceutically acceptable derivative thereof, which is

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(67.) The compound of any one of the above (42.) to (44.), (60.), or (62.) to (65.) or a pharmaceutically acceptable derivative thereof, which is

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(68.) The compound of any one of the above (42.), (43.), (47.), or (54.) to (59.) or a pharmaceutically acceptable derivative thereof, which is

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(69.) The compound of any one of the above (42.), (43.), (46.), or (54.) to (59.) or a pharmaceutically acceptable derivative thereof, which is

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(70.) The compound of any one of the above (42.), (43.), (46.), (54.), or (57.) to (59.) or a pharmaceutically acceptable derivative thereof, which is

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(71.) The compound of any one of the above (42.), (43.), or (47) or a pharmaceutically acceptable derivative thereof, which is

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(72.) The compound of any one of the above (42.), (43.), (46.), (54.), or (56.) to (59.) or a pharmaceutically acceptable derivative thereof, which is

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(73.) The compound of any one of the above (42.), (43.), (46.), (60.), or (63.) to (65.) or a pharmaceutically acceptable derivative thereof, which is

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(74.) The compound of any one of the above (66.) to (73.), which is a free base.

(75.) The compound of any one of the above (66.) to (73.), which is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof.

(76.) A composition comprising the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof and a pharmaceutically acceptable carrier or excipient.

(77.) A method for treating pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof.

(78.) A method for treating pain, pain associated with osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof.

(79.) A method for treating pain, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof.

(80.) A method for treating pain, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof.

(81.) A method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of the compound of any one of the above (42.) to (75.) or a pharmaceutically acceptable derivative thereof.

(82.) The product of combining the compound of any one of the above (42.) to (74.) with fumaric acid, where the molar ratio in the product is about 1:0.5 of (the Compound of Formula (I)):(fumaric acid).

(83.) A composition comprising the product of the above (82.) and a pharmaceutically acceptable carrier or excipient.

(84.) A method for treating pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (82.).

(85.) A method for treating pain, pain associated with osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (82.).

(86.) A method for treating pain, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (82.).

(87.) A method for treating pain, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the product of the above (82.).

(88.) A method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of the product of the above (82.).

(89.) A compound which is

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or a pharmaceutically acceptable derivative thereof.

(90.) A composition comprising the compound of the above (89.) or a pharmaceutically acceptable derivative thereof and a pharmaceutically acceptable carrier or excipient.

(91.) A method for treating pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of the above (89.) or a pharmaceutically acceptable derivative thereof.

(92.) A method for treating pain, pain associated with osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of the above (89.) or a pharmaceutically acceptable derivative thereof.

(93.) A method for treating pain, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of the above (89.) or a pharmaceutically acceptable derivative thereof.

(94.) A method for treating pain, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of the compound of the above (89.) or a pharmaceutically acceptable derivative thereof.

(95.) A method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of the compound of the above (89.) or a pharmaceutically acceptable derivative thereof.

(96.) The compound of any one of the above (1.) to (95.) or a pharmaceutically acceptable derivative thereof, wherein the % ee of the compound is at least about 90%.

(97.) The compound of any one of the above (1.) to (96.) or a pharmaceutically acceptable derivative thereof, wherein the % ee of the compound is at least about 93%.

(98.) A compound, product or a pharmaceutically acceptable derivative thereof or composition of any one of the above (1.) to (29.), (35.), (36.), (42.) to (76.), (82.), (83.), (89.), (90.), (96.), or (97.) for use in the treatment of pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal.

(99.) A compound, product or a pharmaceutically acceptable derivative thereof or composition of any one of the above (1.) to (29.), (35.), (36.), (42.) to (76.), (82.), (83.), (89.), (90.), or (96.) to (98.) for use in the treatment of pain in an animal.

(100.) A compound, product or composition of any one of the above (1.) to (29.), (35.), (36.), (42.) to (76.), (82.), (83.), (89.), (90.), or (96.) to (98.) for use in the treatment of pain associated with osteoarthritis in an animal.

(101.) A compound, product or a pharmaceutically acceptable derivative thereof or composition of any one of the above (1.) to (29.), (35.), (36.), (42.) to (76.), (82.), (83.), (89.), (90.), or (96.) to (98.) for use in the treatment of osteoarthritis in an animal.

(102.) Use of a compound, product or composition of any one of the above (1.) to (29.), (35.), (36.), (42.) to (76.), (82.), (83.), (89.), (90.), or (96.) to (98.) or a pharmaceutically acceptable derivative thereof in the manufacture of a medicament for the treatment of pain, pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS

4.1 Compounds of Formula (I)

The disclosure encompasses Compounds of Formula (I):

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or a pharmaceutically acceptable derivative thereof,

(1) provided that if R₄is —H then m is 1, and

(2) provided that if R₄is —H and the a-b bond is in the (S) configuration, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group, where R₁, R₄, R₈, R₉, and m are as defined above for Compounds of Formula (I).

Certain embodiments of formula (I) are presented below.

In one embodiment, a Compound of Formula (I) is a free base.

In another embodiment, a Compound of Formula (I) is a pharmaceutically acceptable derivative of a Compound of Formula (I).

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a pharmaceutically acceptable salt. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a fumaric acid-salt. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a fumaric acid-salt where the molar ratio of the Compound of Formula (I):fumaric acid is about 1:0.5.

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a co-crystal. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a fumarate co-crystal. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a fumarate co-crystal where the molar ratio of the Compound of Formula (I):fumarate is about 1:0.5.

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (I) is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof. In another embodiment, the molar ratio of the Compound of Formula (I):(fumaric acid and/or fumarate) is about 1:0.5.

Other embodiments relate to the product of combining a Compound of Formula (I) with fumaric acid, where the molar ratio in the product is about 1:0.5 of (the Compound of Formula (I)):(fumaric acid); a composition comprising that product and a pharmaceutically acceptable carrier or excipient; a method for treating pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of that product; and a method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of that product.

In another embodiment, it is further provided that:

(3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group; and (4) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —F, and R₉is —F, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group or a (S)-3-methyl group.

In another embodiment, it is further provided that:

(3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group; and (5) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, R₉is -halo, and m is 1, then the methyl group bonded to the piperazine ring is a (S)-3-methyl group or a (R)-3-methyl group.

In another embodiment, it is further provided that:

(5) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, R₉is -halo, and m is I, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

In another embodiment, it is further provided that:

(3) if R₄is —H, the carbon atom at the a position of the a-b bond is in the (S) configuration, R₈is —H, and R₉is -halo, then the methyl group bonded to the piperazine ring is a (R)-3-methyl group; and (5) if R₄is —CH₃, the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration, R₈is —H, R₉is -halo, and m is 1, then the methyl group bonded to the piperazine ring is a (S)-2-methyl group, a (S)-3-methyl group, or a (R)-3-methyl group.

In another embodiment, it is further provided that:

In another embodiment, R₁is —F, —Cl, —Br, or —CF₃.

In another embodiment, R₁is —F, —Cl, or —CF₃.

In another embodiment, R₁is —F or —CF₃.

In another embodiment, R₁is —Cl or —CF₃.

In another embodiment, R₁is —F or —Cl.

In another embodiment, R₁is —F.

In another embodiment, R₁is —Cl.

In another embodiment, R₁is —CF₃.

In another embodiment, R₁is —Br.

In another embodiment, R₁₀is —CH₃or —CH₂CH₃.

In another embodiment, R₁₀is —CH₂CH₃.

In another embodiment, R₁₀is —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃.

In another embodiment, R₉is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, or —OCH₃.

In another embodiment, R₉is —H, —F, or —OCF₃.

In another embodiment, R₉is —H, —F, or —Cl.

In another embodiment, R₉is —H or —F.

In another embodiment, R₉is —H or —Cl.

In another embodiment, R₉is —H or —CH₃.

In another embodiment, R₉is —F or —CH₃.

In another embodiment, R₉is —F or —Cl.

In another embodiment, R₉is —Cl or —CH₃.

In another embodiment, R₉is —H.

In another embodiment, R₉is —F.

In another embodiment, R₉is —Cl.

In another embodiment, R₉is —CH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃.

In another embodiment, R₈is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, or —OCF₃.

In another embodiment, R₈is —H, —F, —Cl, —CH₃, or —OCH₃.

In another embodiment, R₈is —H, —F, —Cl, or —CH₃.

In another embodiment, R₈is —H, —F, —Cl, or —OCH₃.

In another embodiment, R₈is —H, —F, —Cl, or —OCF₃.

In another embodiment, R₈is —H, —F, or —CH₃.

In another embodiment, R₈is —H, —F, or —OCH₃.

In another embodiment, R₈is —H, —F, or —OCF₃.

In another embodiment, R₈is —H, —F, or —Cl.

In another embodiment, R₈is —H or —F.

In another embodiment, R₈is —H or —Cl.

In another embodiment, R₈is —H or —CH₃.

In another embodiment, R₈is —F or —CH₃.

In another embodiment, R₈is —F or —Cl.

In another embodiment, R₈is —Cl or —CH₃.

In another embodiment, R₈is —H.

In another embodiment, R₈is —F.

In another embodiment, R₈is —Cl.

In another embodiment, R₈is —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, or —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, or —OCH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, or —OCF₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, or —Cl and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H or —F and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H or —Cl and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H or —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —F or —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —F or —Cl and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —Cl or —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —F and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —Cl and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —CH₃and R₈is —H, —F, or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, or —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, or —OCH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, or —OCF₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, or —Cl and R₈is —F or —CH₃.

In another embodiment, R₉is —H or —F and R₈is —F or —CH₃.

In another embodiment, R₉is —H or —Cl and R₈is —F or —CH₃.

In another embodiment, R₉is —H or —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —F or —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —F or —Cl and R₈is —F or —CH₃.

In another embodiment, R₉is —Cl or —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H and R₈is —F or —CH₃.

In another embodiment, R₉is —F and R₈is —F or —CH₃.

In another embodiment, R₉is —Cl and R₈is —F or —CH₃.

In another embodiment, R₉is —CH₃and R₈is —F or —CH₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, or —CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, or —OCH₃and R₈is —F.

In another embodiment, R₉is —H, —F, or —OCF₃and R₈is —F.

In another embodiment, R₉is —H, —F, or —Cl and R₈is —F.

In another embodiment, R₉is —H or —F and R₈is —F.

In another embodiment, R₉is —H or —Cl and R₈is —F.

In another embodiment, R₉is —H or —CH₃and R₈is —F.

In another embodiment, R₉is —F or —CH₃and R₈is —F.

In another embodiment, R₉is —F or —Cl and R₈is —F.

In another embodiment, R₉is —Cl or —CH₃and R₈is —F.

In another embodiment, R₉is —H and R₈is —F.

In another embodiment, R₉is —F and R₈is —F.

In another embodiment, R₉is —Cl and R₈is —F.

In another embodiment, R₉is —CH₃and R₈is —F.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCF₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —Cl, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —F, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —Cl, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —Cl, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl or —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —CH₃, R₈is —F or —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F, and R₈is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCF₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —Cl, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —F, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —Cl, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —Cl, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl or —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —CH₃, R₈is —F, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —OCF₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, or —Cl, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —F, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —Cl, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H or —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F or —Cl, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl or —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —F, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —Cl, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —CH₃, R₈is —CH₃, and R₁is —Cl or —CF₃.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, —C(O)OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, —CH₂OCH₃, or —C(O)OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, —OCH₂CH₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —OCH₂CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, —OCF₃, or —CH₂OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —Br, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, —OCH₃, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, —CF₃, or —OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, —CH₃, or —OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, or —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, or —OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, —Cl, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, or —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, or —OCH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, or —OCF₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, —F, or —Cl, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H or —F, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H or —Cl, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H or —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —F or —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —F or —Cl, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —Cl or —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —H, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —F, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —Cl, R₈is —F, and R₁is —Cl.

In another embodiment, R₉is —CH₃, R₈is —F, and R₁is —Cl.

In another embodiment, R₄is —H.

In another embodiment, R₄is —CH₃.

In another embodiment, R₄is —H and R₁is —F, —Cl, or —CF₃.

In another embodiment, R₄is —CH₃and R₁is —F, —Cl, or —CF₃.

In another embodiment, R₄is —H and R₁is —F or —CF₃.

In another embodiment, R₄is —CH₃and R₁is —F or —CF₃.

In another embodiment, R₄is —H and R₁is —F or —Cl.

In another embodiment, R₄is —CH₃and R₁is —F or —Cl.

In another embodiment, R₄is —H and R₁is —Cl or —CF₃.

In another embodiment, R₄is —CH₃and R₁is —Cl or —CF₃.

In another embodiment, R₄is —CH₃and m is 0.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃and m is 0.

In another embodiment, R₄is —H and m is 1.

In another embodiment, R₄is —CH₃and m is 1.

In another embodiment, R₄is —H, R₁is —F, —Cl, or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, and m is 0.

In another embodiment, R₄is —H, R₁is —Cl or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, and m is 0.

In another embodiment, R₄is —H, R₁is —F or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, and m is 1

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, and m is 0.

In another embodiment, R₄is —H, R₁is —F or —Cl, and m is 1

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, and m is 1

In another embodiment, R₄is —CH₃, R₁is —Cl, and m is 0.

In another embodiment, R₄is —H, R₁is —Cl, and m is 1.

In another embodiment, R₄is —CH₃, R₁is Cl, and m is 1.

In another embodiment, R₄is —CH₃, R₁is —CF₃, and m is 0.

In another embodiment, R₄is —H, R₁is —CF₃, and m is 1.

In another embodiment, R₄is —CH₃, R₁is —CF₃, and m is 1.

In another embodiment, R₄is —H and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F, —Cl, or —CF₃, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F or —CF₃, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F or —Cl, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —Cl or —CF₃, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F, —Cl, or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₁is —H, R₁is —Cl or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —F or —Cl, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —Cl, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H, R₁is —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (S) configuration.

In another embodiment, R₄is —H and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F, —Cl, or —CF₃, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F or —CF₃, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F or —Cl, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —Cl or —CF₃, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F, —Cl, or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —Cl or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F or —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —F or —Cl, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —Cl, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —H, R₁is —CF₃, m is 1, and the carbon atom at the a position of the a-b bond is in the (R) configuration.

In another embodiment, R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is Cl, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃, R₁is —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (S) configuration.

In another embodiment, R₄is —CH₃and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F, —Cl, or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —F or —Cl, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —Cl, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is Cl, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —CF₃, m is 0, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, R₄is —CH₃, R₁is —CF₃, m is 1, and the carbon atoms at the a and c positions of the a-b bond and the c-d bond are each in the (R) configuration.

In another embodiment, m is 1 and the methyl group bonded to the piperazine ring is a (S)-2-methyl group.

In another embodiment, m is 1 and the methyl group bonded to the piperazine ring is a (S)-3-methyl group.

In another embodiment, m is 1 and the methyl group bonded to the piperazine ring is a (R)-3-methyl group.

Aqueous solubility of compounds is often a desirable feature. For example, aqueous solubility of a compound permits that compound to be more easily formulated into a variety of dosage forms that can be administered to an animal. When a compound is not fully soluble in biological fluids, e.g., blood, it can precipitate and the animal's exposure to the drug will accordingly not correspond to the administered dose. Aqueous solubility increases the likelihood that a compound will have higher dissolution and, for compounds with good permeability, it results in high exposure in an animal's blood, and increases the ability to predict exposure at the target sight of the compound.

Many Compounds of Formula (I) are soluble, and in some cases highly soluble, in aqueous solution. For example, at either pH 6.8 or pH 1.2, compound 200 is insoluble in aqueous solution, i.e., has an aqueous solubility <0.1 μM. In contrast, the aqueous solubility at pH 1.2 of the following Compounds of Formula (I) is >50 μM: A126(a), A155(a), A155(d), A155(e), A158(a), C125(r), and C126(r). The aqueous solubility at pH 6.8, in μM, of Compounds of Formula (I) A126(a), A155(a), A155(d), A155(e), A158(a), C125(r), and C126(r) is 14, 17, 4.0, 5.0, 5.0, 3.0, and 4.0, respectively. Additionally, the aqueous solubility at either pH 1.2 or pH 6.8 of Compound of Formula (I) A122(a) is >50 μM. The aqueous solubility, in μM, at pH 1.2 of compounds 209, 210, 211, 212, 213, 214, and 215 is 9.3, 2.0, 1.3, 10.3, 39.6, >50 and 9.6, respectively. The following compounds are aqueous insoluble at pH 6.8: 203, 207, 200, and 208. The following compounds have low aqueous solubility at pH 6.8: 209, 210, 211, 212, 213, 214, and 215 have aqueous solubility, in μM, of 1.0, 0.4, 0.4, 1.9, 0.8, 1.8, and 0.6, respectively.

The following chemical structures relate to certain of the above-discussed compounds:

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4.2 Compounds of Formula (II)

Preferred Compounds of Formula (I) are Compounds of Formula (II):

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or a pharmaceutically acceptable derivative thereof,

where R₄, R₈, and R₉are as defined above for Compounds of Formula (II).

Certain embodiments of formula (II) are presented below.

In one embodiment, a Compound of Formula (II) is a free base.

In another embodiment, a Compound of Formula (II) is a pharmaceutically acceptable derivative of a Compound of Formula (II).

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a pharmaceutically acceptable salt. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a fumaric acid-salt. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a fumaric acid-salt where the molar ratio of the Compound of Formula (II):fumaric acid is about 1:0.5.

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a co-crystal. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a fumarate co-crystal. In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a fumarate co-crystal where the molar ratio of the Compound of Formula (II):fumarate is about 1:0.5.

In another embodiment, the pharmaceutically acceptable derivative of a Compound of Formula (II) is a fumaric acid-salt, a fumarate co-crystal, or a combination thereof. In another embodiment, the molar ratio of the Compound of Formula (II):(fumaric acid and/or fumarate) is about 1:0.5.

Other embodiments relate to the product of combining a Compound of Formula (II) with fumaric acid, where the molar ratio in the product is about 1:0.5 of (the Compound of Formula (II)):(fumaric acid); a composition comprising that product and a pharmaceutically acceptable carrier or excipient; a method for treating pain, e.g., pain associated with osteoarthritis, osteoarthritis, UI, an ulcer, IBD, or IBS in an animal, comprising administering to an animal in need thereof, an effective amount of that product; and a method of inhibiting TRPV1 function in a cell comprising contacting a cell capable of expressing TRPV1 with an effective amount of that product.