NOVEL COMPOUNDS, ISOMER THEREOF, OR

PHARMACEUTICALLYACCEPTABLE SALTS THEREOFAS

VANILLOID RECEPTOR ANTAGONIST; AND PHARMACEUTICAL

COMPOSITIONS CONTAINING THE SAME

TECHNICAL FIELD ;

The present disclosure relates to novel compounds, isomer thereof or pharmaceutically acceptable salts thereof as TRPVl antagonist; and a i pharmaceutical composition containing the same. j i 1

BACKGROUND ART I

The vanilloid receptor- 1 (VRl, or transient receptor potential vanilloid-1,

TRPVl) is the receptor for capsaicin (8-methyl-N-vaniHyl-6-nonenamide|), a pungent ingredient in hot peppers. The molecular cloning of TRPVl was reported in 1997 (Caterina et al, 1997, Nature, 389, ρρ816-824), which belongs to the TRP j channel family of non-selective cation channel. TRPVl is activated or sensitized

I by stimuli such as capsaicin, resiniferatoxin, heat, acid, anandamide, lipid metabolites or the like; thus it plays a crucial role as a molecular integrator of noxious stimuli in mammals (Tominaga et al, 1998, Neuron, 21 pp531-J543; Hwang et al, 2000, PNAS, 97, pρ6155-6160). The TRPVl is highly expressed in primary afferent sensory neurons, and also reportedly expressed in varjious organs and tissues such as bladder, kidney, lung, intestine, skin, central nervous i system (CNS), and non-neuronal tissues (Mezey et al., 2000, PNAS, 91, pp3655-

3660; Stander et al, 2004, Exp. Dermatol 13, ρpl29-139; Cortright et al, 2Q01, BBRC, 281, ppll83-1189), and besides TRPVl protein is upregulated in painful disease conditions. Activation of the TRPVl by endogenous/exogenous stimuli leads to not only transmission of noxious stimuli, but also liberation of neuropeptides such as substance P, CGRP (Calcitonin Gene-Related Peptide) in the neurons, thereby causing neurogenic inflammation. TRPVl knock-out mice

show normal responses in a wide range of behavioural tests including noxious mechanical and acute thermal stimuli, but exhibit little thermal hypersensitivity in inflammation states. (Caterina et al, 2000, Science, 288, pp306-313; Davis et al, 2000, Nature, 405, ppl83-187; Karai et al, 2004, J. Clin. Invest., 113, ppl344- 1352).

As mentioned above, the TRPVl knock-out mice exhibit reduced responses to thermal or noxious stimuli, which has been supported by the effects of TRPVl antagonists in various animal models of pain (Immke et al., 2006, Semin. Cell. Dev. Biol, 17(5), pp582-91; Ma et al., 2007, Expert Opin. Ther. Targets, 11(3), pp307-20). The well-known TRPVl antagonist, capsazepine, decreases hyperalgesia caused by physical stimuli in several models of inflammatory and neuropathic pain (Walker et al., 2003, JPET, 304, pp56-62; Garcia-Martinez et al, 2002, PNAS, 99, 2374-2379). In addition, treatment of the primary culture of afferent sensory neurons with the TRPVl agonist, capsaicin etc., results in damage to nerve functions and furthermore death of nerve cells. The TRPVl antagonist exerts defense actions against such damage to nerve functions and nerve cell death (Holzer P., 1991, Pharmacological Reviews, 43, ppl43-201; Mezey et al., 2000, PNAS, 97, 3655-3660). The TRPVl is expressed on sensory neurons distributed in all regions of the gastrointestinal tract and is highly expressed in inflammatory disorders such as irritable bowel syndrome and inflammatory bowel disease (Chan et al., 2003, Lancet, 361, pp385-391; Yiangou et al, 2001, Lancet, 357, ρpl338-1339). In addition, activation of the TRPVl stimulates sensory nerves, which in turn causes release of neuropeptides which are known to play a critical role in pathogenesis of gastrointestinal disorders such as gastroesophageal reflux disease (GERD) and stomach duodenal ulcer (Holzer P., 2004, Eur. J. Pharmacol. 500, pρ231-241; Geppetti et al, 2004, Br. J. Pharmacol, 141, ppl313-1320).

The TRPVl -expressing afferent nerves are abundantly distributed in airway mucosa, and bronchial hypersensitivity is very similar mechanism to hyperalgesia. Protons and lipoxygenase products, known as endogenous ligands for the TRPVl, are well known as crucial factors responsible for development of asthma and chronic obstructive pulmonary diseases (Hwang et al, 2002, Curr.

Opin. Pharmacol. pp235-242; Spina et ah, 2002, Curr. Opin. Pharmacol. pp264- 272). Moreover, it has been reported that air-polluting substances which are a kind of asthma-causing substances, i.e., particulate matter specifically acts on the TRPVl and such action is inhibited by capsazepine (Veronesi et ah, 2001, NeuroToxicology, 22, pp795-810). Urinary bladder hypersensitiveness and urinary incontinence are caused by various central/peripheral nerve disorders or injury, and TRPVl expressed in afferent nerves and urothelial cells play an important role in bladder inflammation. (Birder et ah, 2001, PNAS, 98, ρpl3396-13401). Further, TRPVl knock-out mice are anatomically normal but have higher frequency of low-amplitude, non-voiding bladder contractions and reduced reflex voiding during bladder filling as compared to wild type mice, which is thus indicating that the TRPVl affects functions of the bladder (Birder et ah, 2002, Nat. Neuroscience, 5, pp856-860). The TRPVl is distributed in human epidermal keratinocytes as well as in primary afferent sensory nerves (Denda et ah, 2001, Biochem. Biophys. Res. Commun., 285, ppl250-1252; Inoue et ah, 2002, Biochem. Biophys. Res. Commun., 291, ppl24-129), and it is then involved in transmission of various noxious stimuli and pains such as skin irritation and pruritus, thereby having close correlation with etiology of dermatological diseases and disorders, such as skin inflammation, due to neurogenic/non-neurogenic factors. This is supported by the report that the TRPVl antagonist, capsazepine inhibits inflammatory mediators in human skin cells (Southall et ah, 2003, J. Pharmacol. Exp. Ther., 304, pp217-222). Over recent years, evidence has been accumulation on other roles of TRPVl. TRPVl might be involved in the blood flow/pressure regulation via sensory vasoactive neuropeptide release and in the regulation of plasma glucose levels or in the pathogenesis of type 1 diabetes (Inoue et ah, Cir. Res., 2006, 99, pp 119-31; Razavi et ah, 2006, Cell, 127, pρll23-35; Gram et ah, 2007, Eur. J. Neuroscl, 25, ρp213-23). Further, it is reported that TRPVl knock-out mice show less anxiety-related behavior than their wild type littermates with no differences in locomotion (Marsch et ah, 2007, J. Neurosci., 27(4), pp832-9).

Based on the above-mentioned information, development of various TRPVl antagonists is under way, and some patents and patent applications

relating to TRPVl antagonists under development were published. (Szallasi et al, 2007, Nat. Rev. Drug Discov., 6, ρp357-72; Appendino et al, 2006, Progress in Medicinal Chemistry, 44, ppl45-180; Rami et al, 2004, Drug Discovery Today: Therapeutic Strategies, I ₅ pp97-104; Correll et al, 2006, Expert Opin. Ther. Patents, 16, pp783-795; Kyle et al, 2006, Expert Opin. Ther. Patents, 16, pp977- 996)

Compounds of the present disclosure, are useful for prophylaxis and treatment of diseases associated with the activity of TRPVl (Nagy et al., 2004, Eur. J. Pharmacol. 500, 351-369) including but not limited to, pain such as acute pain, chronic pain, neuropathic pain, post-operative pain, rheumatic arthritic pain, osteoarthritic pain, postherpetic neuralgia, neuralgia, headache, dental pain, pelvic pain, migraine, bone cancer pain, mastalgia and visceral pain (Petersen et ah, 2000, Pain 88, pρl25-133; Walker et al., 2003, J. Pharmacol. Exp. Ther., 304, pp56-62; Morgan et al, 2005, J. Orofac. Pain, 19, pp248-60 ; Dinis et al, 2005, Eur. Urol., 48, ppl62-7; Akerman et al, 2004, Br. J. Pharmcol, 142, ppl354- 1360; Ghilardi et al, 2005, J. Neuroscl, 25, 3126-31; Gopinath et al, 2005, BMC Womens Health, 5, 2-9) ; nerve-related diseases such as neuropathies, HIV-related neuropathy, nerve injury, neurodegeneration, and stroke (Park et al, 1999, Arch. Pharm. Res. 22, pρ432-434; Kim et al, 2005, J. Neuroscl 25(3), ρp662-671); diabetic neuropathy (Kamei et al, 2001, Eur. J. Pharmacol 422, pp83-86); fecal urgency; irritable bowel syndrome (Chan et al, 2003, Lancet, 361, pp385-391); inflammatory bowel disease (Yiangou et al, 2001, Lancet 357, ppl338-1339); gastrointestinal disorders such as gastro-esophageal reflux disease (GERD), stomach duodenal ulcer and Crohn's disease (Holzer P, 2004, Eur. J. Pharm., 500, pp231-241; Geppetti et al, 2004, Br. J. Pharmacol, 141, ppl313-1320); respiratory diseases such as asthma, chronic obstructive pulmonary disease, cough (Hwang et al, 2002, Curr. Opin. Pharmacol. ρp235-242; Spina et al, 2002, Curr. Opin. Pharmacol. pp264-272; Geppetti et al, 2006, Eur. J. Pharmacol, 533, pp207-214 ; McLeod et al, 2006, Cough, 2, 10); urinary incontinence (Birder et al, 2002, Nat. Neuroscience 5, pp856-860); urinary bladder hypersensitiveness (Birder et al, 2001, PNAS, 98, ρpl3396-13401); neurotic/allergic/inflammatory skin diseases such as psoriasis, pruritus, prurigo and dermatitis (Southall et al,

2003, J. Pharmacol. Exp. Ther,, 304, pρ217-222); irritation of skin, eye or mucous membrane (Tominaga et al, 1998, Neuron 21 pp531-543); hyperacusis; tinnitus; vestibular hypersensitiveness (Balaban et al, 2003, Hear Res. 175, pp 165-70); cardiac diseases such as myocardial ischemia (Scotland et al., 2004, Circ. Res. 95, ppl027-1034; Pan et al., 2004, Circulation 110, ppl826-1831); haemorrhagic shock (Akabori et al., 2007, Ann. Surg., 245(6), pp964-70); hair growth-related disorders such as hirsutism, effluvium, alopecia (Bodό et al., 2005, Am. J. Patho. 166, pp985-998; Birό et al, 2006, J. Invest. Dermatol, ppl-4); rhinitis (Seki et al., 2006, Rhinoϊogy, 44 _? pp 128-34); pancreatitis (Hutter et al, 2005, Pancreas, 30, pp260-5); cystitis (Dinis et al, 2004, J. Neurosci., 24, pp 11253-63; Sculptoreanu et al, 2005, Neurosci. Lett. 381, pp42-6); vulvodynia (Tympanidis et al.,, 2004, Eur. J. Pain, 8, ppl2-33); psychiatric disorders such as anxiety or fear (Marsch et al, 2007, J. Neurosci., 21 (A), pp832-9).

Compounds that are related to VRl activities are discussed e.g. in WO 02/61317, WO 02/090326, WO 02/16318, WO 02/16319, WO 03/053945, WO 03/099284, WO 03/049702, WO 03/049702, WO 03/029199, WO 03/70247, WO 04/07495, WO 04/72068, WO 04/035549, WO 04/014871, WO 04/024154, WO 04/024710, WO 04/029031, WO 04/089877, WO 04/089881, WO 04/072069, WO 04/111009, WO 05/03084, WO 05/073193, WO 05/05139O ₅ WO 05/049613, WO 05/049601, WO 05/047280, WO 05/047279, WO 05/044802, WO 05/044786, WO 06/097817, WO 06/098554, WO 06/100520, WO 06/101321, WO 06/102645, WO 06/103503, WO 06/111346, WO 06/101321, WO 06/101318, WO 06/1113769, WO 06/116563, WO 06/120481, WO 06/122250, WO 06/122799, WO 06/129164, WO 06/51378, WO 06/95263, WO 07/42906, WO 07/45462, WO 07/50732, WO 07/54474, WO 07/54480, WO 07/63925. WO 07/65663, WO 07/65888, WO 07/67619, WO 07/67710, WO 07/67711, WO 07/67756, WO 07/67757, WO07/63925, WO07/65662, WO07/65663, WO07/65888, WO07/69773, US20070149517, or US20070149513.

More specificically, WO 06/101321 and WO 06/101318 relate to VRl modulators with a biphenyl partial structure. As a result of extensive and intensive studies, the present inventors have consequently synthesized novel

compounds having VRl antagonistic activity. Said new compounds have biphenylic structures, wherein one phenyl ring is substituted in para position to its attachment position to the rest of the molecule with a trifluoromethyl group or a fluoro, and has at least one additional substituent in ortho position (relative to said attachment position). Compared to the specific compounds disclosed in WO 06/101321 or WO 06/101318, which do not show this particular combination of features, the present compounds show remarkable improvement of their physicochemical characteristics, such as metabolic stability or pharmacokinetic profiles. Therefore, it is an object of the present disclosure to provide novel compounds useful as a potent antagonist for a TRPVl, isomer thereof and pharmaceutically acceptable salts thereof; and a pharmaceutical composition comprising the same.

DETAILED DESCRIPTION OFTHE DISCLOSURE

The present disclosure provides a novel compound of the following formula (Ia), an isomer, or a pharmaceutically acceptable salt thereof:

formula (Ia) wherein,

A iS -C=C- Or -CH-CH-;

Ri is hydrogen, or C1-C3 alkyl;

R ₂ and R ₃ are independently hydrogen, halogen, cyano, C1-C3 alkyl, C1-C3 alkoxy, halo(Cl-C3)alkyl, (C2-C5)alkenyl, or (C2-C5)alkynyl; R ₄ is halo(Cl-C3)alkyl or halogen;

R ₅ is C2-C10 alkyl, C2-C10 alkoxy, C1-C5 alkoxy (C1-C5) alkoxy, C1-C5 alkoxy (C1-C5) alkylamino, C2-C10 alkylamino, di(Cl-C5 alkyl)amino, C3-C6 cycloalkylamino, C3-C6 cycloalkoxy, or (C3-C6)cycloalkyl(Cl-C3)alkyloxy; and

R ₆ is hydrogen, Cl-ClO alkyl, Cl-ClO alkoxy, or Cl-ClO alkylamino.

The present disclosure also provides a novel compound of the following formula (I), an isomer, or a pharmaceutically acceptable salt thereof:

formula (I) wherein,

R ₁ is hydrogen, methyl, or ethyl;

R ₂ and R ₃ are independently hydrogen, halogen, cyano, methyl, ethyl, methoxy, trifluoromethyl, vinyl, or acetylenyl; R ₄ is trifluoromethyl or fluoro;

R ₅ is C2-C5 alkyl, C2-C5 alkoxy, C1-C2 alkoxy (C1-C3) alkoxy, C1-C2 alkoxy

(C1-C3) alkylamino, C2-C5 alkylamino, di(Cl-C3 alkyl)amino, C3-C6 cycloalkylamino, C3-C6 cycloalkoxy, or (C3-C6)cycloalkyl(Cl-C3)alkyloxy; and

R ₆ is hydrogen, C1-C5 alkyl, C1-C5 alkoxy, or C1-C5 alkylamino.

Another aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; as described above wherein If R ₅ is ethoxy, butoxy, pentoxy, (C3-C6)cycloalkoxy, or (C3-C6)cycloalkyl(Cl-C3)alkyloxy, then R ₁ is methyl. In another embodiment in the compounds of formula (Ia) or (I) as disclosed further above, if R ₅ is ethoxy, butoxy, or pentoxy, and R4 is simultaneously fluoro, then Ri is methyl.

In another embodiment in the compounds of formula (Ia) or (I) as disclosed further above, if R ₅ is ethoxy, butoxy, or pentoxy, then R4 is trifluoromethyl. In this specific embodiment, Ri is preferably methyl.

Another aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, Ri is hydrogen; R ₂ is halogen; and R ₅ is C2-C4 alkyl or C2-C4

alkylamino.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable . salt thereof; wherein, Ri is hydrogen; R ₂ is fluoro; R ₃ is hydrogen, fluoro, cyano, methyl, vinyl, or acetylenyl; R ₄ is trifluoromethyl; R ₅ is C2-C4 alkyl or C2-C4 alkylamino; and

R ₆ is hydrogen.

Another aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₁ is hydrogen, methyl, ethyl, or preferably methyl.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, Ri is methyl; R ₂ is halogen; and R ₅ is C2-C4 alkyl, C2-C4 alkyloxy, or C2-C4 alkylamino.

Another aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein,

Ri is methyl;

R ₂ is fluoro;

R ₃ is hydrogen, fluoro, vinyl, methyl, or acetylenyl;

R ₅ is C2-C4 alkyl, C2-C4 alkyloxy, or C2-C4 alkylamino; and R ₆ is hydrogen or C1-C3 alkyl.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₂ and R ₃ are independently hydrogen, fluoro, cyano, methyl, ethyl, methoxy, trifluoromethyl, vinyl, acetylenyl, or preferably hydrogen, fluoro, cyano, methyl, vinyl, or acetylenyl.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₂ and R ₃ are both fluoro.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I) ₅ an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₄ is fluoro, or preferably trifluoromethyl.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₅ and R ₆ are both C1-C3 alkyl; or preferably methyl, ethyl, or propyl; or more preferably propyl.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₆ is hydrogen.

One aspect of the present disclosure is a compound according to the above formula (Ia) or (I), an isomer, or a pharmaceutically acceptable salt thereof; wherein, R ₅ is ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, ethylamino, propylamino, isopropylamino, n-butylamino, isobutylamino, sec-butylamino, or cyclohexylmethoxy, provided that if R ₅ is ethoxy, butoxy, pentoxy, or cyclohexylmethoxy, then R ₁ is methyl.

Another aspect of the present disclosure is a compound of the formula (Ia) or (I) as further described herein, an isomer, or a pharmaceutically acceptable salt thereof, wherein, if Ri is methyl or ethyl, then the compound may be a pure enantiomer or may be a mixture of the (R) and (S)-enantiomer; and then, the C- atom to which Ri is attached is preferably in the (Reconfiguration.

Another aspect of the present disclosure is compounds of the formula (Ia)

or (I) as further described herein, an isomer, or a pharmaceutically acceptable salt thereof wherein,

R ₅ is C2-C5 alkyl, (C2~C5)alkyloxy, C1-C4 alkylamino, or (C3-

C6)cycloalkylalkoxyoxy, wherein preferably, R ₅ is C2-C4 alkyl, (C2-C4)alkyloxy, or C2-C4 alkylamino; wherein particularly preferably,

R ₅ is C2-C4 alkyl, or C1-C3 alkylamino; wherein particularly preferably,

R ₅ is ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, ethoxy, propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, ethylamino, n-propylamino, isopropylamino, n-butylamino, isobutylamino, sec-butylamino, or cyclohexylmethoxy, wherein particularly preferably,

R ₅ is C2-C4 alkyl, propoxy, isopropoxy, or C2-C4 alkylamino; wherein even more preferably,

R ₅ is ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, propoxy, isopropoxy, ethylamino, n-propylamino, isopropylamino, n-butylamino, isobutylamino, or sec-butylamino, wherein even more preferably,

R ₅ is n-propyl, n-butyl, isobutyl, isopropoxy, sec-butoxy, ethylamino, n- propylamino, isopropylamino, n-butylamino, wherein more preferably,

R ₅ is n-propyl, n-butyl, isobutyl, n-propoxy, ethylamino, propylamine, isopropylamino, n-butylamino, wherein even more preferably,

R ₅ is propyl, butyl, isobutyl, ethylamino, propylamino, or isopropylamino, wherein even more preferably,

R ₅ is propyl, butyl, ethylamino, propylamino, or isopropylamino.

Preferred examples of compounds according to the disclosure are selected from the group consisting of:

N- [ 1 -(3 , 5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl]-3 -(2-ρropylamino-4- trifluoromethyl-phenyl)-acrylamide,

N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-propy lamino-4- trifluoromethyl-phenyl)-acrylamide,

(i?)-3-(2-Butylamino-4-trifluoromethyl-ρhenyl)-N-[l-(3,5 -difluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

(R)-N- [ 1 -(3 ,5 -Difluoro-4-methanesulfonylamino-ρhenyl)-ethyl] -3 -(2-propoxy-4- trifluoromethyl-phenyl)-acrylamide,

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-eth yl]-3-(2,6-dipropyl-

4-trifluoromethyl-phenyl)-acrylamide, (R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl] -3-(2-ethoxy-4- trifluoromethyl-phenyl)-acrylamide, (R)-N-[ 1 -(3 ,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl]-3 -(2- ethylamino-4-trifluoromethyl-phenyl)-acrylamide,

N-(3-Fluoro-4-methanesulfonylamino-5-methyl-benzyl)-3-(2- propylamino-4- trifluoromethyl-phenyl)-acrylamide,

N-(3-Fluoro-4-methanesulfonylamino-5-vinyl-benzyl)-3-(2-p ropylamino-4- trifluoromethyl-phenyl)-acrylamide,

N-(3 -Cyano-5 -fluoro-4-methanesulfonylamino-benzyl)-3 -(2-propylamino-4- trifluoromethyl-phenyl)-acrylamide, N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2-pr opoxy-4- trifluoromethyl-phenyl)-acrylamide,

(R)-3-(2,6-Dibutyl-4-trifluoromethyl-phenyl)-N-[l-(3,5-di fluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

(R)-3-(2,6-Diethyl-4-trifluoromethyl-ρhenyl)-N-[l-(3,5-d ifluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-ethyl amino-4- trifluoromethyl-phenyl)-acrylamide,

3 -(2-Ethylamino-4-trifluoromethyl-phenyl)-N-(3 -fluoro-4- methanesulfonylamino-5-methyl-benzyl)-acrylamide, N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-isopropo xy-4- trifluoromethyl-phenyl)-acrylamide,

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-eth yl]-3-(2-propyl-4- trifluoromethyl-phenyl)-acrylamide,

N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-propy l-4-trifluoromethyl- phenyl)-acrylamide,

N-(3-Fluoro-4-methanesulfonylamino-5-methyl-benzyl)-3-(2- propyl-4- trifluoromethyl-phenyl)-acrylamide,

(R)-3-(2-Butyl-4-trifluoromethyl-ρhenyl)-N-[l-(3,5-difluoro -4- methanesulfonylamino-phenyl)-ethyl]-acrylamide ₅

(R)-N-[ 1 -(3,5 -Difluoro-4-methanesulfonylamino-ρhenyl)-propyl] -3 -(2-propyl-4- trifluoromethyl-phenyl)-acrylamide, (i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-ρhenyl)-ethy l]-3-(2-isoρropoxy-

4-trifluoromethyl-phenyl)-acrylamide,

(R)-N-[l-(3,5-DifluoiO-4-metlianesulfonylamino-phenyl)-et hyl]-3-(4-fluoro-2- propoxy-phenyl)-acrylamide,

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-eth yl]-3-(4-fluoro-2- propylamino-phenyl)-acrylamide,

(R)-3-(2-Butoxy-4-trifluoromethyl-ρhenyl)-N-[l-(3,5-difl uoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

(R)-3 -(2-Butoxy-4-fluoro-pheny I)-N- [ 1 -(3 , 5-difluoro-4-methanesulfonylamino- phenyl)-ethyl] -acrylamide, N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2-pr opyl-4- trifluoromethyl-phenyl)-acrylamide,

(R)-3 -(2-Butyl-4-trifluoromethyl-ρhenyl)-N- [ 1 -(3 -fluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

(R)-3-(2-sec-Butoxy-4-trifluoromethyl-phenyl)-N-[l-(3,5-d ifluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide,

(R)-3-(2-sec-Butoxy-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4 - methanesulfonylamino-phenyl)-ethyl]-acrylamide, (R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-ρhenyl)-ethyl ]-3-(2- ethylamino-4-fluoro-phenyl)-acrylamide, N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-ethylamm o-4-fluoro- phenyl)-acrylamide,

(R)-N-(2-Fluoro-4-{ l-[3-(2-propyl-4-trifluoromethyl-phenyl)-allylaπiino]-ethyl }- phenyl)-methanesulfonamide ₅

(R)-3-(2-Butylamino-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4 - methanesulfonylamino-phenyl)-ethyl]-acrylamide,

3-(2-Butylamino-4-fluoro-phenyl)-N-(3,5-difluoro-4-methan esulfonylamino- benzyl)-acrylamide,

(i?)~N-[l-(3,5-Difluoro-4-methanesulfonylamino-ρhenyl)-ethy l]-3-(2-isobutyI-4- trifluoromethyl-phenyl)-acrylamide ₃

(R)-3-(2-Cyclohexylmethoxy-4-trifluoromethyl-phenyl)-N-[l -(3,5-difluoro- 4methanesulfonylamino-phenyl)-ethyl]-acrylamide, (i?)-N-[l-(3,5-Difluoro-4-methanesulfonylammo-phenyl)-ethyl] -3-(4-fIuoro-2- ρropyl-phenyl)-acrylamide,

N-(3-Fluoro-4-methanesulfonylamino-5-vinyl-benzyl)-3-(2-isop ropylamino-4- trifluoromethyl-phenyl)-acrylamide ₅ and

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-eth ylJ-3-(2- propylamino-4-trifluoromethyl-phenyl)-propionamide.

Particularly preferred examples of compounds according to the disclosure are selected from the group consisting of:

N-[ 1 -(3 , 5-Difluoro-4-methanesulfonylamiiio-phenyl)-ethyl] -3 -(2-propylamino-4- trifluoromethyl-phenyl)-acrylamide,

(R)-3-(2-Butylamino-4-trifluoromethyl-phenyl)-N-[l-(3,5-d ifluoro-4-methane sulfonylamino-phenyl)-ethyl]-acrylamide,

(i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-et hyl]-3-(2-propoxy-4- trifluoromethyl-ρhenyl)-acrylamide, (i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl ]-3-(2,6-dipropyl-

4-trifluoromethyl-ρhenyl)-acrylamide,

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-eth yl]-3-(2-ethoxy-4- trifluoromethyl-phenyl)-acrylamide,

(R)-N- [ 1 -(3 , 5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl]-3 -(2-ethylamino- 4-trifIuoromethyl-phenyl)-acrylarnide,

N-(3-Fluoro-4-methanesulfonylamino-5-methyl-benzyl)-3-(2- propylamino-4- trifluoromethyl-phenyl)-acrylamide,

N-(3-Fluoro-4-methanesulfonylamino-5-vinyl-benzyl)-3-(2-prop ylamino-4- trifluoromethyl-phenyl)-acrylamide, N-(3-Cyano-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2-pro� �ylamino-4- trifluoromethyl-phenyl)-acrylamide ₅

(R)-3 -(2, 6-Diethyl-4-trifluoromethyl-ρhenyl)-N-[ 1 -(3 ,5-difluoro-4-methane

sulfonylamino-phenyl)-ethyl]-acrylamide,

N-(3 , 5 -Difluoro-4-methanesulfonylamino-benzy l)-3 -(2-ethylamino-4-trifluoro methyl-phenyl)-acrylamide ₅

N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-isopr opoxy-4-trifluoro methyl-phenyl)-acrylamide,

(i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-et hyl]-3-(2-propyl-4- trifluoromethyl-phenyl)-acrylamide,

(R)-3-(2-Butyl-4-trifluoromethyl-phenyl)-N-[l-(3,5-difluo ro-4-methanesulfonyl amino-pheny l)-ethy 1] - aery lamide, (R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl] -3-(2-isoρroρoxy-

4-trifluoromethyl-phenyl)-acrylamide,

(R)-3 -(2-Butoxy-4-trifluoromethyl-phenyl)-N- [l-(3.5 -difluoro-4-methanesulfonyl amino-phenyl)-ethyl]-acrylamide,

(i?)-3-(2-Butoxy-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4-me thanesulfonylamino- phenyl)-ethyl]-acrylamide,

N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2 -propyl-4- trifluoromethyl-phenyl)-acrylamide,

(i?)-3-(2-Butyl-4-trifluoromethyl-ρhenyl)-N-[l-(3-fluoro -4-methanesulfonyl amino-phenyl)-ethyl]-acrylamide, (R)-3 -(2-sec-Butoxy-4-trifluoromethyl-pheny I)-N- [ 1 -(3 , 5-difluoro-4-methane sulfonylamino-phenyl)-ethyl]-acrylamide,

(i?)-3 -(2-sec-Butoxy-4-fluoro-pheny I)-N- [ 1 -(3 , 5 -difluoro-4-methanesulfonyl amino-phenyl)-ethyl] -acrylamide,

(i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-et liyl]-3-(2-ethylamino- 4-fluoro-phenyl)-acrylamide,

(R)-N-(2-Fluoro-4- { 1 - [3 -(2-propyl-4-trifluoromethyl-phenyl)-allylamino]-ethyl } - phenyl)-methanesulfonamide,

(R)-3-(2-Butylamino-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4 -methanesulfonyl amino-phenyl)-ethyl]-acrylamide, (i?)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl ]-3-(2-isobutyl-4- trifluoromethyl-phenyl)-acrylamide, and

N-(3 -Fluoro-4-methanesulfonylamino-5 -vinyl-benzyl)-3 -(2-isoproρylamino-4-

trifluoiOmethyl-phenyl)-acrylamide.

The compounds of the formula (Ia) or (I) of the present disclosure can chemically be synthesized by the following reaction schemes. However, these are given only for illustration of the disclosure and not intended to limit to them.

[Scheme 1] 1

The Scheme 1 shows a proposed process for synthesizing acrylamide compound with various substituents. Substituted benzylamine (1) is reacted with phenylacrylic acid (2) to yield benzyl phenylacrylamide (3) using DMTMM {4- (4,6-dimethoxy-l,3,5-triazin-2-yl)-4-methylmorpholinium chloride} (Tetrahedron Lett., 1999, 40, 5327).

[Scheme 2]

The Scheme 2 shows a proposed process for synthesizing acrylamide compound (11) with various substituents. 4-Substituted 2-aminobenzoic acid (5),

which is prepared by hydrogenation of 4-substituted 2-nitrobenzoic acid (4), is converted to the corresponding alkylamino benzoic acid (6) via reductive animation. The substituted benzoic acid (6) is converted to the corresponding Weinreb amide (7), which is reduced by lithium aluminum hydride to yield substituted benzaldehyde (8). The benzaldehyde (8) is converted to methyl phenyl acrylic ester (9) by Wittig reaction. The methyl phenyl acrylic ester (9) is hydrolyzed with lithium hydroxide to yield phenyl acrylic acid (10). The phenyl acrylic acid (10) is reacted with substituted benzylamine (1) as shown in scheme 1 to yield benzyl phenylacrylamide (11).

[Scheme 3]

The Scheme 3 shows a more efficient process for synthesizing alkylamino benzoic acid (6) which is an intermediate to benzyl phenylacrylamide (11). One pot hydrogenation reaction of 4-substituted 2-nitrobenzoic acid (4) in the presence of an aldehyde and acetic acid replaces the two-step process including hydrogenation of 4 and reductive amination of the corresponding 2-aminobenzoic acid 5.

[Scheme 4]

The Scheme 4 shows an alternative process for synthesizing Weinreb amide (7) which is an intermediate to benzyl phenylacrylamide (11). 4-Substituted

2-nitrobenzoic acid (4) is converted to the corresponding Weinreb amide (12).

Hydrogenation of the weinreb amide (12) followed by reductive amination with

an aldehyde yields Weinreb amide (7).

The Scheme 5 shows a proposed process for synthesizing acrylamide compound (20) with various substituents. 4-Substituted 2-hydroxybenzoic acid (13) is reacted with an alkyl halide and potassium carbonate to yield corresponding alkoxy benzoate (14), which is hydrolyzed with lithium hydroxide to give alkoxy benzoic acid (15). The substituted benzoic acid (15) is converted to benzyl phenylacrylamide (20) by similar processes used for benzyl phenylacrylamide (11) shown in Scheme 2.

[Scheme 6]

The Scheme 6 shows an alternative process for synthesizing methyl phenyl acrylic ester (18) which is an intermediate to benzyl phenylacrylamide

(20). 4-Substituted 2-hydroxybenzaldehyde (21) is converted to corresponding methyl phenyl acrylic ester (22) by Wittig reaction, which is reacted with an alkyl

halide and potassium carbonate to yield methyl phenyl acrylic ester (18).

[Scheme 7]

The Scheme 7 shows a proposed process for synthesizing acrylamide compound (25) with various substituents. 4-Triflurometfiyl iodobenzene is converted to substituted phenyl acrylic acid methyl ester (23) by palladium catalyzed coupling reaction. The phenyl acrylic acid methyl ester (23) is hydrolyzed with lithium hydroxide to yield phenyl acrylic acid (24). The phenyl acrylic acid (24) is reacted with substituted benzylamine (1) as described in Scheme 1 to yield benzyl phenylacrylamide (25).

[Scheme 8]

The Scheme 8 shows a proposed process for synthesizing acrylamide compound (32) with various substituents. Substituted benzoyl chloride (26) is reacted with 2-amino-2-methyl-l-propanol in the present of a base, and the resulting adduct is treated with thionyl chloride followed by sodium hydroxide to afford dihydro-oxazole compound (27). After treated with n-butyl lithium at low temperature, the compound 27 is reacted with an alkyl halide to give disubstituted dihydro-oxazole (28). The compound 28 is hydrolyzed with conc-HCl to the corresponding benzoic acid, which is converted to the Weinreb amide (29). After reducing compound 29 with lithium aluminum hydride, the resulting aldehyde is converted to the phenyl acrylic ester (30) under suitable Wittig reaction conditions. The acrylic ester (30) is hydrolyzed with lithium hydroxide to yield the corresponding acrylic acid (31). Substituted benzylamine (1) is reacted with acrylic acid (31) as described in Scheme 1 to yield benzyl phenylacrylamide (32).

[Scheme 9]

The Scheme 9 shows a proposed process for synthesizing amide compound (33) with various substituents. Substituted acrylamide (3) is reduced with PdVC under hydrogen pressure to yield amide compound (33).

The present disclosure also provides to a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof for use as a medicament.

In one embodiment, the present disclosure also provides a pharmaceutical composition comprising a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof as an active ingredient and a pharmaceutically acceptable carrier.

In another embodiment, the present disclosure also provides a composition comprising a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof; and pharmaceutically acceptable carrier for preventing or treating a condition associated with the pathological stimulation and/or aberrant expression of vanilloid receptor.

In one preferred aspect, the present disclosure provides a pharmaceutical composition comprising a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof, for treating a condition selected from the group consisting of pain, inflammatory disease of the joints, neuropathies, HIV- related neuropathy, nerve injury, neurodegeneration, stroke, urinary bladder hypersensitivity including urinary incontinence, cystitis, stomach duodenal ulcer, irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD), fecal urgency, gastroesophageal reflux disease (GERD), Crohn's disease, asthma, chronic obstructive pulmonary disease, cough, neurotic/allergic/inflammatory skin disease, psoriasis, pruritus, prurigo, irritation of skin, eye or mucous membrane, hyperacusis, tinnitus, vestibular hypersensitivity, episodic vertigo, cardiac diseases such as myocardial ischemia, hair growth-related disorders such as effluvium, alopecia, rhinitis, and pancreatitis.

In a particularly preferred aspect, the present disclosure relates to the pharmaceutical composition comprising a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof for treating pain as described above, wherein the pain is or is associated with a condition selected from the group consisting of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, diabetic neuropathic pain, post-operative pain, dental pain, non- inflammatory musculoskeletal pain (including fibromyalgia, myofascial pain syndrome and back pain), visceral pain, migraine, and other types of headaches. The present disclosure also provides a pharmaceutical composition comprising a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof, which is characterized in that it is adapted for oral administration.

In one aspect, the present disclosure relates to the use of a compound of

formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof for the preparation of a medicament

In another aspect, the present disclosure relates to the use of a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof for the preparation of a medicament for the prevention or treatment of a condition that is associated with the aberrant expression and/or aberrant activation of a vanilloid receptor.

In a preferred aspect, the present disclosure relates to the use of a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof, in preparation of a medicament for the prevention or treatment of a condition that is selected from the group consisting of pain, inflammatory disease of the joints, neuropathies, HIV-related neuropathy, nerve injury, neurodegeneration, stroke, urinary bladder hypersensitivity including urinary incontinence, cystitis, stomach duodenal ulcer, irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD), fecal urgency, gastro-esophageal reflux disease (GERD), Crohn's disease, asthma, chronic obstructive pulmonary disease, cough, neurotic/allergic/inflammatory skin disease, psoriasis, pruritus, prurigo, irritation of skin, eye or mucous membrane, hyperacusis, tinnitus, vestibular hypersensitivity, episodic vertigo, cardiac diseases such as myocardial ischemia, hair growth-related disorders such as effluvium, alopecia, rhinitis and pancreatitis.

In a particularly preferred aspect, the present disclosure relates to the use of the compound of formula (Ia) or (I), an isomer thereof, for preparing a medicament for preventing or treating pain as described above, wherein the condition is pain, which is or which is associated with a condition selected from the group consisting of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, diabetic neuropathic pain, post-operative pain, dental pain, non-inflammatory musculoskeletal pain (including fibromyalgia, myofascial pain syndrome and back pain), visceral pain, migraine, and other types of headaches.

In another aspect, the present disclosure relates to a method for inhibiting vanilloid ligand from binding to vanilloid receptor in a patient, comprising

contacting cells expressing vanilloid receptor in the patient with the compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof.

In another aspect, the present disclosure relates to a method for preventing or treating a condition associated with the pathological stimulation and/or aberrant expression of vanilloid receptors.

In another aspect, the present disclosure also provides a method for preventing or treating a condition selected from the group consisting of pain, inflammatory disease of the joints, neuropathies, HIV-related neuropathy, nerve injury, neurodegeneration, stroke, urinary bladder hypersensitivity including urinary incontinence, cystitis, stomach duodenal ulcer, irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD), fecal urgency, gastro-esophageal reflux disease (GERD), Crohn's disease, asthma, chronic obstructive pulmonary disease, cough, neurotic/allergic/inflammatory skin disease, psoriasis, pruritus, prurigo, irritation of skin, eye or mucous membrane, hyperacusis, tinnitus, vestibular hypersensitivity, episodic vertigo, cardiac diseases such as myocardial ischemia, hair growth-related disorders such as effluvium, alopecia, rhinitis, and pancreatitis, which comprises administering to a mammal including a person in need thereof a therapeutically effective amount of the compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof.

In a particularly preferred aspect, the present disclosure relates to the method of treating pain by administering a compound of formula (Ia) or (I), an isomer thereof, or a pharmaceutically acceptable salt thereof as described above, wherein the pain is or is associated with a condition selected from the group consisting of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, diabetic neuropathic pain, post-operative pain, dental pain, non-inflammatory musculoskeletal pain (including fibromyalgia, myofascial pain syndrome and back pain), visceral pain, migraine, and other types of headaches

Hereinafter, the formulating methods and kinds of excipients will be described, but the present disclosure is not limited to them.

A compound of formula (Ia) or (I), an isomer thereof or a pharmaceutically acceptable salt thereof according to the present disclosure can be prepared as a pharmaceutical composition containing pharmaceutically acceptable carriers, adjuvants, diluents and the like. For instance, the compounds of the present disclosure can be dissolved in oils, propylene glycol or other solvents which are commonly used to produce an injection. Suitable examples of the carriers include, but not limited to, physiological saline, polyethylene glycol, ethanol, vegetable oils, isopropyl myristate, etc. For topical administration, the compounds of the present disclosure can be formulated in the form of ointment or cream.

The compound according to the present disclosure may also be used in the forms of pharmaceutically acceptable salts thereof, and may be used either alone or in combination or in admixture with other pharmaceutically active compounds. The compounds of the present disclosure may be formulated into injections by dissolving, suspending or emulsifying in water-soluble solvent such as saline and 5% dextrose, or in water-insoluble solvents such as vegetable oils, synthetic fatty acid glyceride, higher fatty acid esters and propylene glycol. The formulations of the disclosure may include any of conventional additives such as dissolving agents, isotonic agents, suspending agents, emulsifiers, stabilizers and preservatives.

The preferable dose level of the compounds according to the present disclosure depends upon a variety of factors including the condition and body weight of the patient, severity of the particular disease, dosage form, and route and period of administration, but may appropriately be chosen by those skilled in the art. The compounds of the present disclosure are preferably administered in an amount ranging from 0.001 to 100 mg/kg of body weight per day, and more preferably from 0.01 to 30 mg/kg of body weight per day. Doses may be administered once a day, or several times a day with each divided portions. The compounds of the present disclosure are used in a pharmaceutical composition in an amount of 0.0001 — 10% by weight, and preferably 0.001 — 1% by weight, based on the total amount of the composition.

The pharmaceutical composition of the present disclosure can be

administered to a mammalian subject such as rat, mouse, domestic animals, human being and the like via various routes. The methods of administration which may easily be expected include oral and rectal administration; intravenous, intramuscular, subcutaneous, intrauterine, duramatral and intracerebroventricular injections.

DETAILED DESCRIPTION QF THE DEFINITIONS

When describing the compounds, pharmaceutical compositions containing such compounds, methods of using such compounds and compositions, and use of such compounds and compositions, all terms used in the present application shall have the meaning usually employed by a relevant person skilled in the art, e.g. by a medicinal chemists, pharmacist or physician. By the way of example some definitions of specific groups are given below: "Alkenyl" includes monovalent olefmically unsaturated hydrocarbyl groups being straight-chained or branched and having at least 1 double bond. "Alkenyl" has preferably 2-5 carbon atoms ("C1-C5 alkenyl"), 2-4 carbon atoms ("C2-C4 alkenyl"), or only 2-3 carbon atoms ("C2-C3 alkenyl"). Particular alkenyl groups include ethenyl (-CH=CH ₂ ), n-propenyl (-CHaCH=CH ₂ ), isopropenyl (C (CH ₃ ) =CH ₂ ), and the like. A preferred "alkenyl" group is ethenyl (vinyl).

"Alkoxy" includes the group -OR wherein R is "alkyl" as defined further above. Particular alkoxy groups include, by way of example, methoxy, ethoxy, n- propoxy, isopropoxy, n-butoxy, tert-butoxy, iso-butoxy, sec-butoxy, n-pentoxy, 1,2-dimethyIbutoxy, and the like.

"Alkoxyalkoxy" refers to the group -OROR', wherein R and R' are the same or different "alkyl" groups as defined further above.

"Alkoxyalkylamino" refers to the group -NH(ROR'), wherein R and R' are the same or different "alkyl" groups as defined further above. "Alkyl" includes monovalent saturated aliphatic hydrocarbyl groups. The hydrocarbon chain may be either straight-chained or branched. "Alkyl" has 1-6 carbon atoms ("C1-C6 alkyl"), and in some instances preferably 1-5 carbon atoms

("C1-C5 alkyl"), 1-4 carbon atoms ("C1-C4 alkyl"), or only 1-3 carbon atoms ("C1-C3 alkyl"). This term is exemplified by groups such as methyl, ethyl, n- propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, t-amyl, and the like.

"Alkynyl" includes acetylenically unsaturated hydrocarbyl groups being straight-chained or branched and having at least 1 triple bond. "Alkynyl" has preferably 2-6 carbon atoms ("C2-C6 alkynyl"), and in some instances even more preferably 2-5 carbon atoms ("C1-C5 alkynyl"), 2-4 carbon atoms ("C2-C4 alkynyl"), or only 2-3 carbon atoms ("C2-C3 alkynyl"). A preferred alkynyl group is ethynyl (acetylenyl). "Alkylamino" includes the group -NHR ¹ , wherein R ¹ is alkyl group as defined herein.

"Dialkylamino" includes the group -NR'R", wherein R' and R" are alkyl group as defined herein.

"Cycloalkyl" refers to cyclic saturated aliphatic hydrocarbyl groups. The numbers of C-atoms referenced in connection with a given cycloalkyl group corresponds to the number of ring forming carbon atoms, e.g. "C3-C6 cycloalkyl" refers to a cycloalkyl with between three and six ring-forming C atoms. Examples of "cycloalkyl" are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl etc. If indicated, a "cycloalkyl" group may be unsubstituted or substituted with one or more alkyl groups, e.g. with C1-C6 alkyl groups, preferably with C1-C3 alkyl groups, particularly preferably with methyl groups. If a "cycloalkyl" carries more than one alkyl substituent these substituents may be attached to the same or to different ring-forming carbon atoms.

"Cycloalkoxy" refers to the group -OR, wherein R is "cycloalkyl" group as defined further above.

"Cycloalkylamino" refers to the group -NHR, wherein R is "cycloalkyl" group as defined further above.

"Cycloalkylalkoxy" refers to the group -OR-R', wherein R is "alkyl" group and R' is "cycloalkyl" group as defined further above. Examples of "cycloalkylalkoxy" are cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclopropylethoxy, etc.

"Cyano" refers to the radical -C≡N

"Ethenyl" or "vinyl" refers to -CH=CH ₂ which is also designated "vinyl" in the present application.

"Ethynyl" or "acetylenyl" refers to -C≡CH.

"Halo" or "halogen" refers to fluoro, chloro, bromo, and iodo. Preferred halo groups are either fluoro or chloro.

"Haloalkyl" includes an "alkyl" group as defined further above which is substituted with one or more halogens which may be the same, e.g. in trifluoromethyl or pentafluoroethyl, or which may be different.

"Isomer" refers to especially optical isomers (for example essentially pure enantiomers, essentially pure diastereomers, and mixtures thereof) as well as conformation isomers (i.e. isomers that differ only in their angles of at least one chemical bond), position isomers (particularly tautomers), and geometric isomers

(e.g. cis-trans isomers).

"Essentially pure", e.g. in connection with enantiomers or diastereomers means at least about 90%, preferably at least about 95%, more preferably at least about 97 or at least about 98%, even more preferably at least about 99%, and particularly preferably at least about 99.5% (w/w) of a specified compound, e.g. a particular enantiomer or diastereomer.

"Pharmaceutically acceptable" means being devoid of substantial toxic effects when used in doses usually employed in a medicinal dosage, and thereby being approvable or preferably being approved by a regulatory agency of the Federal or a state government or being listed in the U. S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, and more particularly in humans. "Pharmaceutically acceptable salt" refers to a salt of a compound of the disclosure that is "pharmaceutically acceptable" as further defined herein, and that possesses the desired pharmacological activity of the parent compound. Such salts include: (1) acid addition salts, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid,

benzoic acid,3- (4-hydroxybenzoyl) benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid, 2- hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, 4methylbicyclo [2.2.2]-oct-2-ene-l-carboxylic acid, glucoheptonic acid,3- phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, and the like; or (2) salts formed when an acidic proton present in the parent compound is replaced. "Pharmaceutically acceptable carrier" refers to a diluent, adjuvant, excipient or carrier with which a compound of the disclosure is administered and which is "pharmaceutically acceptable" as further defined herein.

"Preventing" or "prevention" refers to a reduction in risk of acquiring a disease or disorder (i.e., causing at least one of the clinical symptoms of the disease not to develop in a subject that may be exposed to or predisposed to the disease but does not yet experience or display symptoms of the disease).

"Subject" includes humans and non-human mammals. The term "patient" is used interchangeably with "subject" herein and shall include humans and non- human mammals unless specified otherwise. "Therapeutically effective amount" means the amount of a compound that, when administered to a subject for treating a disease, is sufficient to effect such treatment for the disease. The "therapeutically effective amount" can vary depending on the compound, the disease and its severity, and the age, weight, etc., of the subject to be treated. "Treating" or "treatment" of any disease or disorder refers, in one embodiment, to ameliorating the disease or disorder (i.e., arresting or reducing the development of the disease or at least one of the clinical symptoms thereof). In another embodiment "treating" or "treatment" refers to ameliorating at least one physical parameter, which may not be discernible by the subject. In yet another embodiment, "treating" or "treatment" refers to modulating the disease or disorder, either physically, (e. g., stabilization of a discernible symptom),, physiologically,

(e. g., stabilization of a physical parameter), or both. In yet another embodiment,

"treating" or "treatment" refers to delaying the onset of the disease or disorder. In yet another embodiment, "treating" or "treatment" refers to reducing, modifying or removing one or more discernible symptom of a disease or disorder without modulating the cause of the underlying disease.

MODE FOR CARRYING OUT THE DISCLOSURE

The present disclosure is more specifically explained by following examples and experimental examples. However, it should be understood that the extent of the present disclosure is not limited to the following examples and experimental examples

Example 1 : (3f)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl ]-3- (2-propylamino-4-trifluoromethyl-phenyl)-acrylamide

Step 1: Synthesis of 2-amino-4-(trifluoromethyl)-benzoic acid

2-Nitro-4-trifluoromethyl-benzoic acid (3.07 g, 13.0 mmol) was stirred with Pd/C under hydrogen atmosphere for 2 hrs. The reaction mixture was filtered with celite to remove Pd/C. The filterate was concentrated in vacuo. The residue was extracted with CH ₂ Cl ₂ (30 ml x 3) and H ₂ O (30 ml). The combined organic layer was dried over MgSO ₄ and then concentrated to yield title compound (2.66 & 99%). 1H NMR (300MHz, DMSO-d ₆ ): δ 7.82 (d, IH) ₅ 7.02 (s, IH), 7.05(m, IH), 2.41(br, IH)

Step 2: Synthesis of 2-propylamino-4-ftrifluoromethyl)-benzoic acid

2-Amino-4-(trifluoromethyl)benzoic acid (714 mg, 3.48 mmol),

propionylaldehyde (0.27 ml, 3.74 mmol), acetic acid (3.49 mmol) and sodium triacetoxyborohydiϊde (1.12g, 5.25 mmol) were added in THF(40 ml). The reaction mixture was stirred overnight. The reaction mixture was quenched by adding sat. NaHCO ₃ (50 ml). The aqueous mixture was extracted with CH ₂ Cl ₂ (30ml x 3). A combined organic layer was dried over MgSO ₄ , concentrated in vacuo, and purified with column chromatography to yield title compound (155mg, 18%).

¹ H NMR (300MHz, CDCl ₃ ): δ 8.04 (d, IH, J= 8.4 Hz), 6.89 (s, IH), 6.79 (d, IH, J= 8.1 Hz), 3.21 (t, 2H, J= 7.2 Hz), 1.75 (m, 2H), 1.02 (t, 3H, J= 7.8Hz).

Step 3: Synthesis of N-methoxy-N-methyl-2-propylamino-4-trifluoromethyl- benzamide

2-Propylamino-4-(trifluoromethyl)benzoic acid (147 mg, 0.594 mmol) in CH ₂ Cl ₂ WaS reacted with N,O-dimethylhydroxy amine (82 mg), NMM (0.2 ml) and DMTMM (222 mg) at room temperature overnight. The reaction mixture was quenched by adding H ₂ O(3 ml). The reaction solvent was removed under reduced pressure. Water (30 ml) was added to the resulting residue, which was extracted with ethylacetate (30 ml x 3). The combined organic layer was washed with sat. NaHCO ₃ solution (30 ml), IN HCl aqueous solution (30 ml) and brine (30 ml), and then dried over MgSO ₄ . The filterate was concentrated in vacuo. The residue was purified with column chromatography to yield the title compound (98mg,

57%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.43 (d, IH, J= 7.8 Hz) 6,85 (s, IH), 6.82 (d, IH), 3.56(s, 3H), 3.34 (s, 3H), 3.10 (t, 2H, J = 6.9 Hz), 1.71 (m, 2H), 1.01 (t, 3H, J =6.9 Hz).

Step 4: Synthesis of 3-(2-propylamino-4-trifluoromethyl-phenvD-acrylic acid methyl ester

N-Methoxy-N-methyl-2-ρropylamino-4-trifluoromethyl-benza mide (98.3 mg, 0.339 mmol) was reacted with IM lithium aluminum hydride (0.6 ml) in THF

(20ml) at -40 ⁰ C for 1 hr. The reaction mixture was quenched by adding saturated potassium hydrogen sulfate solution. The mixture was stirred for 30min. The reactions solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was extracted with CH ₂ Cl ₂ (30 ml x 3). The combined organic layer was dried over MgSO ₄ and concentrated in vacuo to yield 2-propylamino-4- trifluoromethyl-benzaldehyde (78 mg). 2-Proρylamino-4-trifluoromethyl- benzaldehyde in toluene was reacted with methyl (triphenylphosphoranylidene) acetate (137 mg) at 100 ⁰ C overnight. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was extracted with ethyl acetate (30 ml x 3). The combined organic layer was dried over MgSO ₄ and filtered. The filterate was concentrated in vacuo and purified with column chromatography to yield title compound (67 mg, 69%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.76 (d, IH, J = 15.9 Hz), 7.41 (d, IH, J = 8.1 Hz), 6.92 (d, IH, J = 8.7 Hz), 6.84 (s, IH), 6.38 (d, IH, J = 15.6 Hz), 3.82 (s, 3H), 3.17 (m, 2H), 1.70 (m, 2H), 1.04 (t, 3H ₅ J = 7.8 Hz).

Step 5: Synthesis of 3-(2-propylamino-4-trifluoromethyl-phenyl)-acrylic acid

3-(2-Propylamino-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (67.3 mg, 0.234 mmol) was reacted with aqueous IN LiOH solution (5 ml) in

THF/CH ₃ OH (10ml/5ml) for 1 hr. The reaction solvent removed in vacuo. Water

(30 ml) was added to the resulting residue, which was neutralized with IN HCl solution, an then extracted with ethyl acetate (30ml x 3). The combined organic layer was dried over MgSO ₄ and concentrated in vacuo to yield title compound (55 mg, 0.201 mmol, 86%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.80 (d, IH, J = 15.6 Hz), 7.48 (d, IH, J = 7.5 Hz), 6.82 (s, IH), 6.79 (s, IH), 6.36 (d, IH, J = 15.6 Hz), 3.10 (t, 2H, J = 6.9 Hz), 1.75 (m, 2H), 0.97 (t, 3H, J - 7.5 Hz)

Step 6: Synthesis of ^)-N-[I -(3.5-difluoro-4-methanesulfonylamino-phenyl)- ethvl] _r 3-f2-propylamino-4-trifluoromethyl-phenylVacrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt (70 mg, 0.24 mmol) in THF was reacted with 3-(2-propylamino-4~ trifluoromethyl-ρhenyl)-aerylic acid (55mg, 0.20 mmol), NMM (0.2 ml) and DMTMM (86 mg, 0.34 mmol) at room temperature overnight. The reaction mixture was quenched by adding H ₂ O. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was extracted with ethyl acetate (30 ml x 3). The combined organic layer was dried over MgSO ₄ . The filterate was concentrate under reduced pressure and purified with column chromatography to yield the title compound (35 mg, 59%). 1H NMR (300MHz, CDCl ₃ ): δ 7.79 (d, IH, J = 15 Hz), 7.37 (d, IH, J - 7.8 Hz), 6.96 (d, IH ₅ J = 8.4 Hz), 6.86 (d, IH, J = 8.1 Hz), 6.82 (s, IH), 6.48 (br, IH), 6.33 (d, IH, J = 15.3 Hz), 5.93 (d, IH, J = 7.2 Hz) ₅ 5.15 (t, IH, J = 7.2 Hz), 3.19 (s, 3H) ₅ 3.14 (t, 2H ₅ J = 7.2 Hz), 1.70 (m ₅ 2H) ₅ 0.97 (t, 3H, J - 7.5 Hz) ESI [M-H] ^" : 504

Example 2: N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2- propyIamino-4-trifluoromethyI-phenyI)-acryIamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt (84 mg, 0.308 mmol) was reacted with 3-(2-ρropylamino-4-trifluoromethyl- ρhenyl)-acrylic acid (67 mg, 0.245 mmol), NMM (0.4 ml) and DMTMM (121 mg) to give the title compound (62 mg, 52%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.75 (d, IH, J = 15.6 Hz), 7.33 (d, IH, J = 7.8 Hz), 6.95 (d, IH ₅ J = 8.4 Hz), 6.84 (d, IH, J = 8.1 Hz), 6.79 (s, IH), 6.30 (d, IH, J = 15.6 Hz), 6.03 (br, IH), 4.59 (br, IH, J = 6.9 Hz), 4.50 (d, 2H, J = 6.0 Hz), 3.16 (s,

3H), 3.12 (t, 2H ₅ J = 7.2 Hz), 1.64 (m, 2H), 0.96 (t, 3H, J = 7.5 Hz)

Example 3 : (iJ)-3-(2-Butylamino-4-trifluoromethyl-phenyl)-N-[l-(3,5- difluoro-4-methanesulfonylamino-phenyl)~ethyl]-acrylamide

(R)-N-[4-(l-Amino-ethyl)-2,6-difluoro-phenyl]-methanesulf onamide, HCl salt (25mg, 0.09mmol) was reacted with 3-(2-butylamino-4-trifluoromethyl- phenyl)-acrylic acid (25mg, 0.09mmol) to give the title compound (15mg, 32%) after purification by crystallization from Hex/EtOAc.

¹ R NMR(300MHz, CDCl ₃ ): δ 7.75(d, IH, J =15.3Hz), 7.37(d, IH, J =8.4Hz), 7.00(m, 2H), 6.90(d, IH, J=8.4Hz), 6.83(s, IH), 6.33(d, IH, J =15.3Hz), 6.12(s, IH), 5.83(d, IH, J=7.8Hz), 5.18(m, IH), 4.18(bs, IH), 3.21(s, 3H), 3.17(m, 2H), 1.48(m, 5H) ₃ 0.97(t, 3H, J=7.5Hz). ESI [M-H]-; 518

Example 4: N-(3,5-Difluoro-4-methanesulfonylamino-benzyI)-3-(2-propoxy- 4-trifluoromethyI-phenyl)-acrylamide

Step 1: Synthesis of 2-propoxy-4-trifluoromethyl-benzoic acid propyl ester

2-Hydroxy-4-trifluoromethyl-benzoic acid (673 mg, 3.26 mmol) was reacted with propylbromide (0.85 ml) and K ₂ CO ₃ (1.42 g) in DMF (15 ml) at 65 ⁰ C overnight. The reaction mixture was quenched by adding 10 ml Of H ₂ O. The mixture was extracted with ethylacetate (30 ml x 3). A combined organic layer

was washed with H ₂ O (50 ml x 6) and brine (50 ml), and dried over MgSO ₄ . The filterate was concentrated in vacuo to yield title compound (908 mg, 99%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.83 (d, IH, J = 8.1 Hz), 7.21 (d, IH, J = S.I Hz),

7.15 (s, IH), 4.28 (t, 2H, J = 6.9 Hz), 4.03 (t, 2H, J = 63 Hz), 1.88 (m, 2H), 1.82 (m, 2H), 1.07 (m, 6H)

Step 2: Synthesis of 2-propoxy-4-trifluoromethyl-benzoic acid

2-Propoxy-4-trifluoromethyl-benzoic acid propyl ester (957 mg, 3.44 mmol) was reacted with IN LiOH (10 ml) at room temperature for 4 hrs. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which wasneutralized with 1 N aqueous HCl solution. The aqueous mixture was extracted with ethylacetate (30 ml x 3). A combined organic layer was dried over MgSO ₄ , and concentrated in vacuo to yield quantitatively title compound.

¹ H NMR (300MHz, CDCl ₃ ): δ 8.32 (d, IH, J - 7.8 Hz), 7.40 (d, IH, J = 8.1 Hz),

7.16 (s, IH), 4.28 (t, 2H, J = 6.6 Hz), 1.98 (m, 2H), 1.26 (m, 3H)

Step 3: Synthesis of N-methoxy-N-methyl-2-ρropoxy-4-trifluoromethyl- benzamide

2-Propoxy~4-(trifluoromethyl)benzoic acid (457 mg, 1.93 mmol) in THF was reacted with N,O-dimethylhydroxy amine (378 mg), NMM (0.65 ml) and DMTMM (947mg) at room temperature overnight. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which wasextracted with ethyl acetate (30 ml x 3). The combined organic layer was washed with 1 M NaHCO ₃ (30 ml), IN HCl (30 ml) and brine (30 ml) and dried over MgSO ₄ . The filterate was purified with column chromatography (Hex/EtOAc = 4/1) to yield the title compound (277 mg, 49%). 1H NMR (300MHz, CDCl ₃ ): δ 7.36 (d, IH ₃ J = 7.8 Hz) ₅ 7.25 (d, IH, J = 8.1 Hz), 7.12 (s, IH), 4.01 (t, 2H, J = 6.3 Hz), 3.46 (s, 3H), 3.35 (br, 3H), 1.83 (m, 2H), 1.03 (t, 3H, J = 6.9 Hz)

Step 4: Synthesis of 2-propoxy-4-trifluoromethyl-benzaldehyde

N-Methoxy-N-methyl-2-propoxy-4-trifluoromethyl-benzamide (277 mg) in THF was reacted with 1 M LAH (1 ml) on -50 ⁰ C for 1 hr. The reaction mixture was quenched by adding aqueous potassium hydrogen sulfate (5 ml). The mixture was stirred for 30 min. The reaction solvent was removed in vacuo. Water (30 ml) was added to the resulting residue, which was was extracted with ethyl acetate (30 ml x 3). The combined organic layer was washed with brine (30 ml) and dried over MgSO ₄ and concentrated in vacuo to yield title compound (232 mg, 100%). ¹ H NMR (300MHz, CDCl ₃ ): δ 10.54 (s, IH), 7.93 (d, IH, J - 8.1 Hz), 7.27 (d, IH, J = 8.1 Hz), 7.21 (s, IH), 4.10 (t, 2H, J = 6.6 Hz), 1.91 (m, 2H), 1.10 (t, 3H, J = 7.2 Hz)

Step 5: Synthesis of 3-f2-propoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester

2-Propoxy-4-trifluoromethyl-benzaldehyde (232 mg, 1 mmol) in toluene was reacted with methyl (triphenylphosphoranylidene)acetate (382 mg, 1.14 mmol) at 110 ⁰ C overnight. The reaction solvent was removed under reduced pressure. Water (30 ml) was added to the resulting residue, which was extracted with ethyl acetate (30 ml x3). The combined organic layer was washed with brine (30 ml) and dried over MgSO ₄ . The filterate was purified with column chromatography to yield title compound (198 mg, 69%). 1H NMR (300MHz, CDCl ₃ ): δ 7.98 (d, IH, J = 16.2 Hz), 7.58 (d, IH, J = 8.1 Hz), 7.21 (m, IH), 7.11 (s, IH), 6.60 (d, IH, J = 16.2 Hz), 4.04 (t, 2H, J = 6.0 Hz), 3.81 (s, 3H), 1.91 (m, 2H), 1.09 (t, 3H, J = 7.5 Hz).

Step 6: Synthesis of 3-(2-propoxy-4-trifluoromethyl-phenylVacrylic acid

3-(2-Propoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (198 mg) was reacted with IN LiOH (5 ml) in THF (10 ml) and CH ₃ OH (5 ml) for 1 hr.

The reaction mixture was concentrated in vacuo. Water (30 ml) was added to the resulting residue, which was neutralized with IN HCl solution. The mixture was extracted with ethyl acetate (30 ml x 3). The combined organic layer was dried over MgSO ₄ . The filterate was concentrated in vacuo to yield title compound (136 mg, 72%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.93 (d, IH ₅ J = 16.2 Hz), 7.71 (d, IH, J = 8.4 Hz), 7.21 (m, IH), 7.12 (s, IH), 6.59 (d, IH, J = 16.2 Hz), 4.04 (t, 2H, J = 6.0 Hz), 1.78 (m, 2H), 1.06 (t, 3H, J = 7.5 Hz)

Step 7: Synthesis of N-(3,5-difluoro-4-methanesulfonylamino-benzyl)-3-(2- propoxy-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt

(78 mg, 0.286 mmol) in THF was reacted with 3-(2-propoxy-4-trifluoromethyl- phenyl)-acrylic acid (67 mg, 0.246 mmol), NMM (0.2 ml) and DMTMM (86 mg) to give the title compound (92 mg, 76%) after column chromatography ( Hex/EtOAc = 1/1).

¹ R NMR (300MHz ₅ CDCl ₃ ): δ 7.90 (d, IH, J = 15.9 Hz), 7.52 (d, IH ₅ J = 8.4 Hz),

7.21 (m, IH), 7.06 (s, IH) ₅ 6.93 (d, IH ₅ J = 7.8 Hz), 6.55 (d, IH, J = 16.2 Hz), 5.96 (br, IH) ₅ 4.51 (d, 2H ₅ J - 6.0 Hz), 4.00 (t, 2H, J = 6.0 Hz), 3.16 (s, 3H), 1.87

(m, 2H), 1.04 (t, 3H, J = 7.5 Hz)

ESI [M-H]-: 505

Example 5: (jRj-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyI)-ethy� �]-3- (2-propoxy-4-trifluoromethyI-phenyl)-acryIamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt

(81 mg, 0.28 mmol) was reacted with 3-(2-propoxy-4-trifluoromethyl-phenyl)-

acrylic acid (68 mg, 0.25 mmol), NMM (0.2 ml) and DMTMM (86 mg) at room temperature overnight to yield the title compound (89 mg, 72%) after column chromatography^ Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.92 (d, IH ₅ J = 15.6 Hz), 7.55 (d, IH, J = 7.8 Hz), 7.19 (d, IH, J = 10.8 Hz), 7.10 (s, IH), 6.99 (d, IH ₅ J = 8.7 Hz) ₅ 6.55 (d, IH ₅ J = 15.9 Hz) ₅ 5.99 (br, IH) ₅ 5.78 (br, IH) ₅ 5.19 (m, IH), 4.03 (t ₅ 2H, J = 6.6 Hz), 3.20 (s, 3H), 1.90 (m, 2H), 1.08 (t, 3H ₅ J = 7.5 Hz)

Example 6: (i?)-N-[l-(3 _? 5-Difluoro-4-methaiiesuIfonyIamino-phenyl)-ethyl]-3- (2,6-dipropyl-4-trifluoromethyI-phenyl)-acryIamide

Step 1: Synthesis of 3-(2,6-dipropyl-4-trifluoromethyl-ρhenyl)-acrylic acid methyl ester

In a 100ml flask, 4-iodobenzotrifluoride (Ig, 3.68mmol) was dissolved in 10ml DMF, and Pd(OAc) ₂ (165mg, 0.2eq), K ₂ CO ₃ (2.54g, 5.0eq), KOAc (1.8g, 5.0eq) ₅ norbonylene (692mg, l.Oeq), methyl acrylate (0.33ml, l.Oeq), and iodopropane (3.75g, 6.0eq) were added stepwisely at room temperature. The resulting reaction mixture was stirred for 3 days. After the completion of the reaction, the Na ₂ S ₂ O ₃ solution was poured into the reaction mixture, which was stirred for 30 minutes, extracted with EtOAc 50ml (3 times), and dried with anh.MgSO ₄ . The organic layer was filtered, concentrated in vacuo, and purified with column chromatography (Hexane : EtOAc = 8 : 1) to give the title compound (0.343g, 30%).

¹ H NMR(SOOMHZ, CDCl ₃ ): δ 7.83(d, IH, J= 16.2Hz ), 7.31(s, 2H) ₅ 6.01 (d, IH, J

= 16.2Hz), 3.84(s, 3H), 2.62(m, 4H), 1.58(m, 4H), 0.94(m, 6H).

Step 2: Synthesis of 3-(2,6-dipropyl-4-trifluoromethyl-phenyl)-acrylic acid

3-(2,6-Dipropyl-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (343 mg) was reacted with IN LiOH (5 ml) in THF (10 ml) and CH ₃ OH (5 ml) for 1 hr. The reaction mixture was concentrated in vacuo. Water (30 ml) was added to the resulting residue, which wasneutralized with IN HCl solution. The mixture was extracted with ethyl acetate (30 ml x 3). The combined organic layer was dried over MgSO ₄ . The filterate was concentrated in vacuo to yield title compound (250 mg, 82%).

Step 3: Synthesis of (R)-N-ri~(3,5-difluoro-4-methanesulfonylamino-phenylV ethyl]-3-(2,6-dipropyl-4-trifluoromethyl-phenyl)-acrylamide

(R)-N-[4-(l-Amino-ethyl)-2,6-difluoro-phenyl]-methanesulf onamide, HCl salt (250mg, 0.87mmol) was reacted with 3-(2,6-dipropyl-4-trifluoromethyl- phenyl)-acrylic acid (261mg, 0.87mmol) to give the title compound (181mg,

39%) after purification by crystallization from Hex/EtOAc. 1H NMR(300MHz, DMSO-d6): δ 9.49(s, IH), 8.70(t, IH ₅ J= 7.5Hz), 7.56(d, IH,

J -15.9Hz), 7.42(s, 2H), 7.15(m, 2H), 6.23(d, IH, J =16.2Hz), 5.05(m, IH),

3.05(s, 3H), 2.61(m, 4H), 1.51(m, 4H), 1.41(d, 3H, J=7.2Hz), 0.88(m, 6H).

ESI [M-H] ^" : 531

Example 7: fi?)-N-[l-(3,5-Difluoro-4-methanesulfonylammo-phenyl)-ethyl] -3- (2-ethoxy-4-trifluoromethyl-phenyl)-acryIamide

Step 1 : Synthesis of 2-ethoxy-4-trifluoromethyl-benzoic acid

2-Hydroxy-4-trifluoromethyl-benzoic acid (1.20 g, 5.82 mmol) was reacted with ethyliodide (2.2 eq) and K ₂ CO ₃ (1.69 g) in DMF solution. The reaction mixture was quenched by adding H ₂ O. The mixture was extracted with ethyl acetate (40 ml x 3). A combined organic layer was washed sat NaHCO ₃ solution (30 ml), H ₂ O (40 ml x 5), and brine, and then dried over MgSO ₄ . The filterate was concentrated in vacuo to yield 2-ethoxy-4-trifluoromethyl benzoic acid ethyl ester. The ester obtained above was reacted with 1 N LiOH (15 ml) in THF and CH ₃ OH cosolvent for 2 hrs as described above to yield title compound

(1.2O g, 88%).

¹ H NMR (300MHz, CDCl ₃ ): δ 8.32 (d, IH, J = 8.1 Hz), 7.40 (d, IH, J = 8.1 Hz), 7.26 (s, IH), 4.40 (q, 2H, J = 6.9 Hz), 1.62 (t, 3H, J = 6.9 Hz)

Step 2: Synthesis of N-methoxy-N-methyl-2-ethoxy-4-trifluoromethyl-benzamide

2-Ethoxy-4-trifluoromethyl-benzoic acid (1.20 g, 5.12 mmol) was reacted with N,O-dimethylhydroxy amine (609 mg), NMM (0.95 ml) and DMTMM (1.47 mg) as described above to give the title compound (1.04 g, 73%) after column chromatography (Hex/EtOAc = 5/ 1 ) .

¹ H NMR (300MHz, CDCl ₃ ): δ 7.40 (br, IH), 7.23 (br, IH), 7.10 (s, IH), 4.13 (t, 2H, J = 6.3 Hz) ₅ 3.49 (s, 3H), 3.37 (br, 3H), 1.42 (t, 3H, J = 6.9 Hz)

Step 3: Synthesis of 2-ethoxy-4-trifluoromethyl-benzaldehyde

N-Methoxy-N-methyl-2-ethoxy-4-trifluoromethyl-benzamide (1.04 g) was reacted with 1 M LAH (1 ml) at -40 ⁰ C for 2 hrs as described above to yield title compound (729 mg, 65%)

¹ H NMR (300MHz, CDCl ₃ ): δ 10.52 (s, IH), 7.93 (d, IH, J = 8.1 Hz), 7.27 (d, IH, J = 8.1 Hz), 7.20 (s, IH), 4.21 (q, 2H, J = 6.6 Hz), 1.52 (t, 3H, J = 6.9 Hz)

Step 4: Synthesis of 3-r2-ethoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester

2-Ethoxy-4-trifluoromethyl-benzaldehyde (729 mg, 3.34 mmol) was reacted with methyl (triphenylphosphoranylidene)acetate (1.45 g, 4.34 rnmol) at 110 ⁰ C overnight as described above to yield title compound (476.5 mg, 52%). ¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.97 (d, IH, J = 16.5 Hz), 7.58 (d, IH, J = 16.2 Hz), 7.58 (d, IH, J = 7.8 Hz), 7.21 (m, IH) ₅ 7.11 (s, IH), 6.60 (d, IH, J = 15.9 Hz), 4.14 (q, 2H, J = 6.9 Hz), 3.82 (s, 3H), 1.58 (t, 3H, J = 7.5 Hz)

Step 5: Synthesis of 3-(2-ethoxy-4-trifluoromethyl-phenylVacrylic acid

3-(2-Ethoxy-4-trifluoromethyl-ρhenyl)-acrylic acid methyl ester (477 mg, 1.74 mmol) was reacted with IN LiOH (7.5 ml) in THF and CH ₃ OH for 1.5 hrs as described above to yield title compound (440 mg, 97%)

¹ H NMR (300MHz, CDCl ₃ ): δ 8.07 (d, IH, J = 16.2 Hz), 7.62 (d, IH, J = 8.1 Hz), 7.26 (m, IH), 7.12 (s, IH), 6.62 (d, IH, J = 16.2 Hz), 4.16 (q, 2H, J = 6.9 Hz), 1.52 (t, 3H, J = 6.9 Hz)

Step 6: Synthesis of ffi)-N-ri-(3,5-difluoro-4-methanesulfonylamino-phenyl)- ethyl]-3-(2-ethoxy-4-trifluoromethyl-phenyπ-acrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt

(70 mg, 0.24 mmol) was reacted with 3-(2-ethoxy-4-trifluoromethyl-phenyl)- acrylic acid (59 mg, 0.22 mmol), NMM (0.2 ml) and DMTMM (73 mg, 0.26 mmol) to give the title compound (77 mg, 69%) after column chromatography

(Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.94 (d, IH, J = 15.9 Hz), 7.56 (d, IH, J = 8.1 Hz),

7.19 (d, IH, J = 8.1 Hz), 7.09 (s, IH), 6.75 (d, IH, J = 8.1 Hz), 6.57 (d, IH, J = 15.9 Hz), 6.08 (br, IH), 5.87 (d, IH, J = 7.8 Hz), 5.20 (t, IH) 4.13 (q, 2H, J = 6.9

Hz), 3.20 (s, 3H), 1.52 (t, 3H, J = 7.5 Hz)

ESI [M-H] ^" : 491

Example 8: N-(3,5-Difluoro-4-methanesulfonyIamino-benzyϊ)-3-(2-ethoxy- 4- trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt

(60 mg, 0.22 mmol) was reacted with 3-(2-emoxy-4-trifluoromethyl-phenyl)- acrylic acid (52 mg, 0.20 mmol), NMM (0.2 ml) and DMTMM (73 mg, 0.25 mmol) at room temperature to yield the title compound (50 mg, 52%) after column chromatography (Hex/EtOAc = 1/1). 1H NMR (300MHz, CDCl ₃ ): δ 7.94 (d, IH, J = 15.6 Hz), 7.56 (d, IH, J = 7.8 Hz), 7.21 (d, IH ₅ J = 7.8 Hz), 7.11 (s, IH), 7.00 (m, 2H), 6.77 (d, IH, J = 8.4 Hz), 6.62 (d, IH, J = 15.9 Hz), 6.03 (br, IH), 4.56 (d, 2H, J = 6.0 Hz), 4.15 (q, 2H, J = 7.2 Hz), 3.21 (s, 3H), 1.48 (t, 3H, J = 7.2 Hz)

Example 9: f2?>N-[l-(3-Fluoro-4-methanesulfonylamino-phenyl)-ethyl]- 3-(2- ethoxy-4-trifluoromethyl-phenyl)-acrylamide

(R)-N-(4-Aminoethyl-2-fluoro-phenyl)-methanesulfonamide, HCl salt (60 mg, 0.22 mmol) was reacted with 3-(2-ethoxy-4-trifluoromethyl-phenyl)-acrylic acid (51 mg, 0.19 mmol), NMM (0.2 ml) and DMTMM (72 mg) at room temperature overnight to yield the title compound (62 mg, 0.13 mmol, 68%) after column chromatography (Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.91 (d, IH, J = 15.6 Hz), 7.55 (m, IH), 7.44 (m, IH), 7.15 (d, IH, J = 9.0 Hz), 7.08 (s, IH), 6.93 (m, IH), 6.55 (d, IH, J = 15.0

Hz), 5.95 (br, IH), 5.87 (d, IH, J = 7.8 Hz), 5.21 (t, IH) 4.14 (q, 2H ₃ J = 6.9 Hz),

3.02 (s, 3H), 1.53 (t, 3H, J = 7.5 Hz)

Example 10: (3?j-N-[l-(3,5-Difluoro-4-methanesu]fonyIamino-phenyI)-ethyI ]- 3-(2-ethyIamino-4-trifluoromethyl-phenyl)-acryIamide

Step 1: Synthesis ofN-methoxy-N-methyl-2-nitro-4-trifluoromethyl-benzamide

2-Nitro-4-trifluoromethyl-benzoic acid (2.753 mg, 11.7 mmol) in THF was reacted with N,O-dimethylhydroxy amine (1.277 g, 13.1 mmol), NMM (3 ml) and DMTMM (3.34 g) at room temperature overnight. The reaction mixture was quenched by adding H ₂ O. The mixture was extracted with ethyl acetate (50 ml x 3). The combined organic layer was washed IM NaHCO ₃ (50 ml x 2), 3% HCl (50 ml x 2) and brine (50 ml), and then dried over MgSO ₄ . The fϊlterate was concentrated in vacuo to yield the title compound (2.84 g, 87%). 1H NMR (300MHz, CDCl ₃ ): δ 8.43 (s, IH), 7.99 (d, IH, J = 8.1 Hz), 7.69 (d, IH, J = 7.8 Hz), 3.39 (s, 6H)

Step 2: Synthesis of 2-amino-N-methoxy-N-methyl-4-trifluoromethyl-benzamide

N-Memoxy-N-methyl-2-nitro-44rifluoromethyl-benzamide (2.54 g, 9.12 mmol) was reacted with Pd/C (441 mg) under hydrogen atmosphere as described above to yield title compound.

¹ H NMR (300MHz, CDCl ₃ ): δ 7.47(d, IH, J = 7.8 Hz), 6.93 (s, IH), 6.91 (d, IH, J

= 7.8 Hz), 3.56 (s, 3H), 3.36 (s, 3H).

Step 3: Synthesis of 2-ethylamino-N-methoxy-N-methyl-4-trifluoromethyl- benzamide

2-Amino-N-methoxy-N-methyl-4-trifluoromethyl-benzamide (482 mg,

1.94 mmol) was reacted with acetaldehyde (0.12 ml, 2.14 mmol) and sodium acetoxyborohydride (892 mg, 4.20 mmol) in CH ₂ Cl ₂ at room temperature as described above to yield title compound (95 mg, 17%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.44 (d, IH, J = 8.1 Hz), 6.86 (s, IH), 6.84 (d, IH, J = 7.8 Hz), 3.57 (s, 3H), 3.35 (s, 3H), 3.18 (q, 2H ₅ J =6.9 Hz), 1.28 (t, 3H, J = 7.2 Hz).

Step 4: Synthesis of 2-ethylammo-4-trifluoromethyl-benzaldehyde

2-Ethylamino-N-methoxy-N-methyl-4-trifluoromethyl-benzami de (95 mg,

0.343 mmol) was reacted with LAH in THF at -40 ⁰ C for 1.5 hrs as described above to yield title compound (22 mg, 29%) after column chromatography (hexane/ethylacetate = 20/1). 1H NMR (300MHz, CDCl ₃ ): δ 9.88 (s, IH), 8.35 (br, IH), 7.57 (d, IH, J = 7.8 Hz), 6.88 (s, IH), 6.87 (d, IH ₅ J = 7.8 Hz), 3.30 (q, 2H, J =6.9 Hz), 1.35 (t, 3H, J = 7.2 Hz).

Step 5: Synthesis of 3-(2-ethylamino-4-trifluoromethyl-phenyl)-acrylic acid

2-Ethylamino-4-trifluoromethyl-benzaldehyde (22 mg) was reacted with methyl (triphenylphosphoranylidene)acetate (49 mg, 0.14 mmol) at 110 ⁰ C overnight as described above to yield 3-(2-ethylamino-4-trifluoromethyl-phenyl)- acrylic acid methyl ester. 3-(2-Ethylamino-4-trifiuoromethyl-phenyl)-acrylic acid methyl ester was reacted with IN LiOH (5 ml) as described above to yield the title compound (20.2 mg)

¹ U NMR (300MHz, CDCl ₃ ): δ 7.87 (d, IH, J = 15.6 Hz), 7.45 (d, IH, J = 8.1 Hz), 6.94 (d, IH, J = 7.8 Hz), 6.86 (s, IH), 6.39 (d, IH, J = 15.6 Hz) ₅ 3.27 (q, 2H, J = 7.2 Hz), 1.35 (t, 3H, J = 7.2 Hz).

Step 6: Synthesis of ^J-N-ri-β^-difluoro^-methanesulfonylamino-phenyl)- ethvn-3-(2-ethylamino-4-trifluoromethyl-phenyl)-acrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt (31 mg, 0.108 mmol) was reacted with 3-(2-ethylamino-4-trifluoromethyl- phenyl)-acrylic acid (20mg, 0.078 mmol), NMM (0.1 ml) and DMTMM (27 mg) to give the title compound (11 mg, 29%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.79 (d, IH, J - 15 Hz) ₅ 7.37 (d, IH, J = 7.8 Hz), 6.96 (d, IH, J = 8.1 Hz), 6.62 (s, IH), 6.48 (br, IH), 6.33 (d, IH, J = 15.3 Hz), 5.52 (d, IH), 5.18 (t, IH), 3.16 (s, 3H), 3.14 (t, 2H, J = 7.2 Hz), 1.70 (m, 3H), 1.35 (t, 3H, J = 7.5 Hz) ESI [M-H] ^" : 490

Example 11 : N-(3-Fluoro-4-methanesulfonylamino-5-methyl-benzyl)-3-(2- propylamino-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2-fluoro-6-methyl-phenyl)-methanesulfonamid e, HCl salt (25 mg) was reacted with 3-(2-propylamino-4-trifluoromethyl-phenyl)-acrylic acid (24 mg, 0.086 mmol), NMM (0.1 ml) and DMTMM (27 mg) at room temperature overnight to yield the title compound (21 mg, 50%). 1H NMR (300MHz, CDCl ₃ ): δ 7.80 (d, IH, J = 15.3 Hz), 7.36 (d, IH, J = 8.1 Hz), 7.14 (m, IH), 7.11 (m, IH), 6.88 (m, IH), 6.80 (d, IH, J = 15.3 Hz), 6.15 (t, IH), 4.56 (d, 2H, J = 6.0 Hz), 3.13 (t, 2H, J = 7.2 Hz), 3.02 (s, 3H), 2.24 (s, 3H), 1.70 (m, 2H), 0.96 (t, 3H, J = 7.5 Hz) ESI [M-H]-.- 486

Example 12: N-(3-Fluoro-4-methanesulfonylamino-5-vinyI-benzyl)-3-(2- propylamino-4-trifluoromethyl-phenyI)-acrylamide

N-(4-Aminomethyl-2-fluoro-6-vinyl-phenyl)-methanesulfonamide , HCl salt (36 mg, 0.15 mmol) was reacted with 3-(2-propylammo-4~trifluoromethyl- ρhenyl)-acrylic acid (28 mg, 0.10 mmol), NMM (0.1 ml) and DMTMM (35 mg) at room temperature overnight to yield the title compound (17 mg, 34%) after column chromatography. 1H NMR (300MHz, CDCl ₃ ): δ 7.80 (d, IH, J = 15.3 Hz), 7.38 (m, IH), 7.22 (m, IH), 7.15 (m, IH), 7.11 (m, IH), 6.90 (d, IH, J = 7.2 Hz), 6.83 (s, IH), 6.34 (d, IH, J = 15.0 Hz), 5.95 (br, 2H) ₅ 5.81 (d, IH, J = 17.4 Hz), 5.46 (d, IH ₅ J = 10.8 Hz), 4.58 (d, 2H, J = 6.0 Hz), 3.16 (t, 2H ₉ J = 6.0 Hz), 3.08 (s, 3H), 1.69 (m, 2H), 1.03 (t, 3H ₅ J = 7.5 Hz) ESI [M-H] ^" : 498

Example 13: N-(3-Cyano-5-fluoro-4-methanesulfonylamino-ben2yl)-3-(2- propylamino-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2-fluoro-6-cyano-phenyl)-methanesulfonam ide, HCl salt (26 mg, 0.092 mmol) was reacted with 3-(2-propylammo-4-trifIuoromethyl- phenyl)-acrylic acid (20 mg, 0.073 mmol), NMM (0.1 ml) and DMTMM (28 mg) at room temperature overnight to yield the title compound (8 mg, 22%) after column chromatography.

¹ H NMR (300MHz, CDCl ₃ ): δ 7.82 (d, IH, J = 4.7 Hz), 7.45 (m, IH), 7.40 (m,

IH), 7.37 (m, IH), 7.21 (s, IH), 7.11 (m, IH) ₅ 6.90 (d, IH, J = 7.8 Hz), 6.84 (s, IH), 6.36 (d, IH, J = 15.0 Hz), 6.10 (br, IH), 4.58 (d, 2H, J = 6.3 Hz), 3.32 (s, 3H) ₅ 3.16 (t, 2H, J = 6.0 Hz) ₅ 1.69 (m, 2H) ₅ 1.03 (t, 3H, J = 7.5 Hz) ESI [M-H]-: 497

Example 14: N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2- propoxy-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2-ethynyl-6-fluoro-phenyl)-methanesulfonami de ₅ HCl salt (53 mg, 0.19 mmol) was reacted with 3-(2-ρroρoxy-4-trifluoromethyl- ρhenyl)-acrylic acid (49 mg, 0.18 mmol), NMM (0.1 ml) and DMTMM (60 mg) at room temperature overnight to yield the title compound (63 mg, 70%) after column chromatography (Hex/EtOAc = 1/1). 1H NMR (300MHz, CDCl ₃ ): δ 7.96 (d, IH, J = 15.6 Hz), 7.56 (d, IH, J = 7.8 Hz), 7.30 (s, IH), 7.20 (m IH), 7.11 (d, IH, J = 7.5 Hz), 6.97 (s, IH) ₅ 6.61 (d, IH, J = 15.9 Hz), 6.41 (br, IH), 6.03 (br, IH), 4.54 (d, IH, J = 6.3 Hz) ₅ 4.03 (t, 2H, J = 6.6 Hz), 3.48 (s, IH) ₅ 3.26 (s, 3H), 1.85 (m, 2H) ₅ 1.06 (t, 3H, J = 7.5 Hz)

Example 15: 3-(2-Ethoxy-4-trifluoromethyI-phenyl)-N-(3-fluoro-4- methanesulfonyIamino-5-trifluoromethyl-benzyl)-acrylamide

N-(4-Aminomethyl-2-fluoro-6-trifluoromethyl-phenyl)- methanesulfonamide, HCl salt (61 mg, 0.19 mmol) was reacted with 3-(2-ethoxy- 4-trifluoromethyl-phenyl)-acrylic acid (45 mg, 0.17 mmol), NMM (0.1 ml) and

DMTMM (64 mg, 0.22 mmol) at room temperature to yield the title compound (63 mg, 0.12 mmol, 69%) after column chromatography (Hex/EtOAc = 1/1). ¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.95 (d, IH ₅ J = 15.6 Hz), 7.56 (d, IH, J = 7.5 Hz), 7.40 (m, IH), 7.19 (d, IH ₅ J = 8.1 Hz), 7.10 (s, IH), 6.63 (d, IH, J = 15.6 Hz), 6.22 (br, IH), 4.60 (d, 2H, J = 6.0 Hz), 4.12 (q, 2H, J = 7.2 Hz), 3.28 (s, 3H), 1.50 (t, 3H, J = 7.2 Hz).

Example 16: (i?)-3-(2,6-Dibutyl-4-trifluoromethyl-phenyl)-N-[l-(3,5-difl uoro- 4-methanesuIfonylamino-phenyl)-ethyl]- acrylamide

(R)-N-[4-(l-Amino-ethyl)-2,6-difluoro-phenyl]-methanesulf onamide, HCl salt (43mg, 0.15mmol) was reacted with 3-(2,6-dibutyl-4-trifluoromethyl-ρhenyl)- acrylic acid (50mg, 0.15mmol) to give the title compound (30mg, 35%) after purification by crystallization from Hex/EtOAc.

¹ H NMR(300MHz, CDCl ₃ ): δ 7.80(d, IH, J = 15.9Hz) ₅ 7.29(s, IH), 7.26(s, 2H), 7.05(10, 2H), 6.02(s, IH), 5.95(d, IH ₅ J =15.9Hz), 5.74(s, IH), 5.34(s, IH), 5.21(m, IH) ₅ 3.22(s, 3H), 2.63(m, 4H) ₅ 1.32(m, HH), 0.91(m, 6H). ESI [M+H]+:

Example 17: (λ)-3-(2,6-Diethyl-4-trifluoromethyl-phenyl)-N-[l-(3,5-difl uoro- 4-methanesuIfonylamino-phenyl)-ethyl]- acrylamide)

(R)-N-[4-(l -Amino-ethyl)-2 ₅ 6-difluoro-phenyl]-methanesulfonamide, HCl salt (38mg, 0.13mmol) was reacted with 3-(2,6-diethyl-4-trifluoromethyl-phenyl)- acrylic acid (36mg, 0.13mmol) to give the title compound (20mg, 30%) after purification by crystallization from Hex/EtOAc.

¹ H NMR(SOOMHZ, CDCl ₃ ): δ 7.84(d, IH, J= 16.5Hz), 7.29(s, IH), 7.30(s, 2H), 7.01(m, 2H) ₅ 6.06(s, IH), 6.02(d, IH, J ^" =16.2Hz), 5.72(s, IH), 5.30(m, IH), 5.24(m, IH), 3.19(s, 3H), 2.69(m, 4H), 1.24(m, 9H). ESI [M-H] ^" : 503

Example 18: N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2- ethylamino-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-3 ₅ 5-difluoro-phenyl)-methanesulfonamide, HCl salt

(42mg, 0.154mmol) was reacted with 3-(2-ethylamino-4-trifluoromethyl-phenyl)- acrylic acid (40mg, 0.154mmol) to give the title compound (36mg, 49%) after purification by crystallization from Hex/EtOAc. 1H NMR(300MHz, CDCl ₃ ): δ 7.80(d, IH, J = 15Hz), 7.38(m, 2H), 6.95(m, 2H), 6.84(s, IH), 6.35(d, IH, J -15.6Hz), 5.99(s, IH), 4.55(d, 2H, J =6Hz), 3.26(m, 2H), 3.22(s, 3H), 1.33(m, 3H). ESI [M-H] ^" : 476

Example 19: 3-(2-Ethylamino-4-trifluoromethyl-phenyl)-N-(3-fluoro-4- methanesuIfonylamino-5-methyI-benzyl)-acrylamide

N-(4-aminomethyl-3-fluoro-5-methyl-phenyl)-methanesulfona mide, HCl salt (28mg, 0.104mmol) was reacted with 3-(2-ethylamino-4-trifluoromethyl- ρhenyl)-acrylic acid (27mg, 0.104mmol) to give the title compound (29mg, 59%) after purification by crystallization from Hex/EtOAc.

¹ H NMR(SOOMHZ, DMSO-d6): δ 8.59(bs, IH), 7.67(d, IH, /= 15.6Hz), 7.47(m, 2H), 6.88(m, IH), 6.57(d, IH, J =15.6Hz), 6.04(s, IH), 4.40(d, 2H, J =5.4Hz),

3.15(m ₅ 2H), 2.96(s, 3H), 2.20(s, 3H), 1.18(m, 3H). ESI [M+H]+:

Example 20: N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2- isopropoxy-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-3,5-difluoro-phenyl)-methanesulfonamide, HCl salt (14mg, 0.051mmol) was reacted with 3-(2~isopropoxy-4-trifluoromethyl-phenyl)- acrylic acid (14mg, 0.051mmol) to give the title compound (llmg, 40%) after purification by crystallization from Hex/EtOAc.

¹ H NMR(300MHz, DMSO-d6): δ 9.50(s, IH), 8.70(d, IH, J = 7.8Hz), 7.69(m, 2H), 7.24(m, 4H), 6.78(d, IH, J =15.9Hz), 4.85(m, IH), 4.52(d, 2H, J =6.0Hz), 3.02(S ₅ 3H), 1.31(m, 6H). ESI [M-H]-; 491

Example 21: N-[l-(3,5-DiJfluoro-4-methanesuIfonylamino-phenyl)-ethyl]-3- (2- propyl-4-trifluoromethyI-phenyI)-acrylamide

Step 1: Synthesis of 4.4-dimethyl-2-r4-trifluoromethyl-ρhenyl)-4,5-dihvdro- oxazole

To an ice-cold solution of 2-amino-2-methyl-l-propanol (21.4g, 240mmol) and triethylamine (16.8mL, 120mmol) in THF was added dropwise 4- trifluoromethyl benzyl chloride (25.Og, 120mmol). After the addition, the reaction mixture was stirred at O ⁰ C for 30 mins and then stirred at ambient temperature for 8hrs. The precipitate was removed by filtration and the filtrate was concentrated by evaporating the solvent under reduced pressure. The resulting residue was treated dropwise with thionyl chloride with vigorous stirring at O ⁰ C. After complete addition, the reaction mixture was further stirred at ambient temperature for lhr. Ether was poured into the reaction mixture and the precipitate was collected by filtration. The precipitate was dissolved in water and the aqueous solution was hydrolyzed with 10% (w/v) NaOH. The aqueous phase was extracted three times with ether, and the combined organic layer was washed with brine, dried over anhydrous MgSO ₄ , and concentrated under reduced pressure. The crude residue was purified by column chromatography (Hex/EtOAc = 5/1) to yield the title compound (25.4g, 87%). 1H NMR(300MHz, CDCl ₃ ): δ 8.05(d, 2H, J =7.8Hz), 7.66(6, 2H, J =7.8Hz), 4.14(s, 2H), 1.39(s, 6H).

Step 2: Synthesis of N-methoxy-N-methyl-2-propyl-4-trifiuoromethyl-benzamide.

A solution of 4,4-dimethyl-2-(4-trifluoromethyl-phenyl)-4,5-dihydro- oxazole (2.43g, lO.Ommol) in THF was cooled to -78 ⁰ C under argon, and n-BuLi

(2.5M in hexane, 4.OmL, lO.Ommol) was added dropwise to the solution. The resulting dark brown solution was stirred for 2hrs at -6O ⁰ C and then cooled again to -78 ⁰ C, to which was added propyl iodide (1.88mL, 19.0mmol). The reaction mixture was allowed to warm up to room temperature, and then stirred overnight. The reaction was quenched by adding water and the aqueous phase was extracted three times with EtOAc. The combined organic layer was washed with brine, dried over anhydrous MgSO ₄ , and concentrated under reduced pressure to give

dark brown residue.

A mixture of the crude residue obtained above and 6N HCl (5.OmL) was heated at reflux for 8hrs. After cooling to ambient temperature, water was added to the reaction mixture and the aqueous layer was extracted three times with EtOAc. The combined organic layer was washed with water, brine, dried over anhydrous MgSO ₄ , and concentrated under reduced pressure. The resulting residue dissolved in THF was treated with IN LiOH, and the resulting mixture was stirred 18hrs at ambient temperature and then 18hrs at 7O ⁰ C. After cooling, the reaction mixture was acidified with 2N HCl and then extracted three times with chloroform. The combined organic layer was washed with brine, dried over anhydrous MgSO ₄ , and concentrated under reduced pressure to give crude benzoic acid product.

The resulting crude acid was dissolved in dichloromethane, to which were added successively N,O-dimethylhydroxylamine, HCl (630mg, 6.46mmol), NMM (0.7ImL, 6.46mmol), and EDC (990mg, 7.75mmol). The resulting mixture was stirred overnight at ambient temperature and then quenched by adding water. The aqueous layer was extracted three times with EtOAc, and the combined organic layer was washed with brine, dried over anhydrous MgSO ₄ , and concentrated under reduced pressure. The crude residue was purified by column chromatography (Hex/EtOAc = 2/1) to yield the title compound (230 mg, 8%). ¹ H NMR(300MHz, CDCl ₃ ): δ 7.50(s, IH), 7.48(d, IH, J =7.8Hz), 7.36(d, IH, J =7.8Hz), 3.43(bs, 3H), 3.36(bs, 3H) ₅ 2.65(t, 2H ₅ J =7.8Hz) ₅ 1.67(m, 2H) ₅ 0.97(t, 3H, J=7.2Hz).

Step 3: Synthesis of 3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid methyl ester.

To a solution of N-methoxy-N-methyl-2-piOpyl-4-trifluoromethyl- benzamide (230mg ₅ 0.84mmol) in THF (15mL) was added dropwise 1.0M LiAlH ₄ (0.42mL, 0.42mmol) at -78 ⁰ C. The mixture was warmed up to -2O ⁰ C and stirred for 30mins. An aqueous solution of sodium potassium tartrate (10% w/v) was added to the reaction mixture and the resulting mixture was vigorously stirred

for 30 mins, to which was added Et ₂ O. After separation of two phases, the aqueous layer was extracted three times with ether and the combined organic layer was washed with brine, dried over anhydrous MgSO _4; filtered and concentrated under reduced pressure. The product was vacuum dried to yield the 2-propyl-4-tritluoromethyl-benzaldehyde.

To a solution of the aldehyde obtained above in toluene was added methyl (triphenylphosphoranylidene)acetate (285mg, 0.85mmol), and the resulting mixture was heated at 8O ⁰ C for 3hrs. The reaction mixture was diluted with EtOAc, and washed with water and brine. The organic layer was dried over anhydrous MgSO ₄ and concentrated under reduced pressure. The resulting residue was purified by column chromatography (Hex/EtOAc = 4/1) to give the title compound (220mg, 96%).

¹ R NMR(300MHz, CDCl ₃ ): δ 7.98(d, IH, J =15.9Hz), 7.63(d, IH, J =8.4Hz), 7.46(d, IH, J =8.4Hz), 7.45(s, IH), 6.42(d, IH, J =15.9Hz), 3.83(s, 3H), 2.77(t, 2H, J =7.5Hz), 1.63(m, 2H), 0.98(t, 3H, J=7.5Hz).

Step 4: Synthesis of 3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid.

To a suspension of 3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (220mg, 0.8 lmmol) in THF (3mL) was added a solution of IN-LiOH

(6 ml), and the mixture was stirred for 3 hours at room temperature. The reaction mixture was diluted with H ₂ O, which was washed three times with EtOAc, acidified with IN HCl to pH 1~2. The resulting solution was extracted three times with methylene chloride and then dried over anhydrous MgSO ₄ and concentrated in vacuo to give the title compound (155mg, 74%).

¹ B. NMR(300MHz, CDCl ₃ ): δ 8.09(d, IH, J =15.9Hz), 7.67(d, IH, J =7.8Hz), 7.49(d, IH, J=7.8Hz), 7.47(s, IH), 6.44(d, IH, 7=15.9Hz), 2.79(t, 2H, /=7.5Hz), 1.64(m, 2H), 0.99(t, 3H, /=7.5Hz).

Step 5: Synthesis of fRVN-ri-(3.5-difluoro-4-methanesulfonylamino-phenyl)- ethyl] -3 -C2-propyl-4-trifluoromethyl-phenyl)-acrylamide

To a suspension of (i?)-N-[4-(l-amino-ethyl)-2,6-difluoro-phenyl]- methanesulfonamide, HCl salt (67mg, 0.23mmol) in THF (5mL) was added N- methylmorpholine (51 1, 0.46mmol). The mixture was stirred for 5 minutes, to which were added 3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid (60mg, 0.23mmol) and 4-(4,6-dimemoxy[l,3,5]triazin-2-yl)-4-memylmorpholinium chloride hydrate (DMTMM, 76mg, 0.28mmol). The mixture was stirred overnight at room temperature and was concentrated under reduced pressure. The residue was diluted with EtOAc and water. The organic layer was washed with saturated sodium bicarbonate, IN HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by recrystallization from n-Hex/EtOAc to give title compound (83mg, 74%). 1H NMR(300MHz, CD ₃ OD): δ 7.99 (d, IH, J= 15.6 Hz), 7.86 (d, IH, J= 8.7 Hz), 7.60 (bs, 2H), 7.18 (d, 2H, J= 8.7 Hz), 6.75 (d, IH, J= 15.6 Hz), 5.20 (m, IH), 3.17 (s, 3H), 2.90 (t, 2H, J= 7.8 Hz), 1.70 (m, 2 H), 1.61 (d, 3H, J= 7.2 Hz), 1.06 (t, 3H, J= 7.2 Hz). ESI [M-H]-: 489

Example 22 : N-(3,5-Difluoro-4-methanesuIfonyIamino-benzyI)-3-(2-propyI-4 - trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2,5-difluoro-phenyl)-methanesulfonamide, HCl salt

(33mg, 0.12mmol) was reacted with 3-(2-propyl-4-trifluoromethyl-phenyl)- acrylic acid (25mg, 0.097mmol) to give the title compound (30mg, 65%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex). ¹ R NMR(300MHz, CD ₃ OD): δ 8.05 (d, IH, /= 15.6 Hz), 7.87 (d, IH, J= 8.7 Hz), 7.62 (bs, 2H), 7.16 (d, 2H, J = 8.7 Hz), 6.76 (d, IH, J = 15.6 Hz), 4.61 (s, 2H),

3.18 (S ₅ 3H), 2.93 (t, 2H ₅ J= 7.8 Hz) ₅ 1.71 (m, 2 H), 1.09 (t, 3H ₅ J= 7.5 Hz). ESI [M+H] ⁺ :

Example 23: N-(3-Fluoro-4-methanesulfonylamino-5-methyl-benzyl)-3-(2- propyl-4-trifluoromethyl-phenyI)-acrylamide

N-(4-Ammomethyl-2-fluoro-6-methyl-phenyl)-methanesulfonamide , HCl salt (32mg, 0.12mmol) was reacted with 3-(2-propyl-4-trifluoromethyl-phenyl)- acrylic acid (25mg, 0.097mmol) to give the title compound (30mg, 63%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex). 1H NMR(300MHz, CD ₃ OD): δ 8.05 (d, IH, J= 15.6 Hz) ₅ 7.85 (d, IH, J= 8.1 Hz), 7.60 (m, 2H), 7.30 (m, 2H) ₅ 6.74 (d, IH ₅ J= 15.6 Hz), 4.64 (s, 2H), 3.08 (s, 3H), 2.92 (t, 2H, J= 7.5 Hz), 2.38 (d, 3H, J= 2.1 Hz) ₅ 1.72 (m, 2 H) ₅ 1.08 (t, 3H ₅ J = 7.5 Hz).

ESI [M+H] ⁺ :

Example 24: (i?)~3-(2-Butyϊ-4-trifluoromethyl-phenyl)-N- [l-(3,5-difluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

3-(2-Butyl-4-trifluoromethyl-phenyl)-acrylic acid was obtained by the procedure in example 21.

(R)-N-[4-(l-Amino-ethyl)-2 ₅ 6-difluoro-phenyl]-methanesulfonamide, HCl salt (38mg, 0.13mmol) was reacted with 3-(2-butyl-4-trifluoromethyl-phenyl)- acrylic acid (30mg, O.llmmol) to give the title compound (29mg, 43%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex).

¹ H NMR(300MHz, CD ₃ OD): δ 7. 90 (d, IH, J = 15.6 Hz) ₃ 7.76 (d, IH, J = 8.7 Hz), 7.51 (bs, 2H) ₅ 7.08 (d, 2H, J = 8.7 Hz), 6.65 (d, IH, J = 15.6 Hz), 5.10 (m, IH), 3.07 (s, 3H), 2.82 (t, 2H, J= 7.8 Hz), 1.55 (m, 2 H), 1.51 (d, 3H, J= 7.2 Hz), 1.40 (m, 2 H), 0.94 (t, 3H, J= 7.2 Hz). ESI [M-HP: 503

Example 25: (i?)-N-[l-(3,5-Difluoro-4-methanesuIfonylamino-phenyl)- propyI]-3-(2-propyl-4-trifl«ororaethyI-phenyI)-acryIamide

(R)-N-[4-(l-Amino-propyl)-2,6-difluoro-phenyl]-methanesul fonamide, HCl salt (15mg, 0.050mmol) was reacted with 3-(2-propyl-4-trifluoromethyl- phenyl)-acrylic acid (8mg, 0.031mmol) to give the title compound (15mg, 97%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex).

¹ H NMR(300MHz, DMSO-d6): δ 8.65 (d, IH, J- 8.1 Hz), 7.69 (m, 4H), 7.11 (d, 2H, J= 8.4 Hz), 6.75 (d, IH, J= 15.6 Hz), 4.82 (m, IH), 2.98 (s, 3H) ₅ 2.75 (t, 2H, J= 7.8 Hz), 1.71 (m, 2 H), 1.52 (m, 2 H), 1.23 (m, 2 H), 0.89 (m, 6H). ESI [M+H] ⁺ :

Example 26: (R)-N- [l-(3,5-Difluoro-4-methanesuIfonylamino-phenyl)-ethyl]- 3-(2-isopropoxy-4-trifluoromethyl-phenyl)-acrylamide

Step 1 : Synthesis of 2-isopropoxy-4-trifluoromethyl-benzoic acid isopropyl ester

A mixture of 2-hydroxy-4-trifluoromethyl-benzoic acid (500 mg, 2.42 mmol) in DMF (5 mL) was added potassium carbonate (837 mg, 6.06 mmol) and 2-bromopropane (906 mg, 5.33 mmol). The resulting mixture was stirred for 48 hours at 110 °C . The reaction mixture was diluted with EtOAc, which was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by chromatography^ex/EtOAc^S/l) to give the title compound (200 mg, 28 %). ¹ H NMR(300MHz, CDCl ₃ ): δ 7.73 (d, IH, J = 8.1 Hz), 7.19 (d, IH, J = 8.4 Hz), 7.15 (s, IH), 5.31 - 5.29 (m, IH), 4.68 - 4.60 (m, IH), 1.40 (d, 6H, J= 6.9 Hz), 1.36 (d, 6H, J = 6.6 Hz).

Step 2: Synthesis of 2-isoρropoxy-N-methoxy-N-methyl-4-trifluoromethyl- benzamide.

To a suspension of 2-isopropoxy-4-trifluoromethyl-benzoic acid isopropyl ester (35 mg, 0.12 mmol) in THF (1 ml) was added a solution of 0.5 N-LiOH (2 eq), and the resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was acidified with IN HCl, and hthen extracted with EtOAc. The combined organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The

resulting residue was vacuum dried to yield the 2-isopropoxy-4-trifluoromethyl- benzoic acid. To an ice-cold suspension of 2-isopropoxy-4-trifluoromethyl- benzoic acid and N, (9-dimethylhydroxylamine hydrochloride (13 mg, 0.132 mmol) in CH ₂ Cl ₂ (1 mL) was added ν-methylmorpholine (0.015 ml, 0.132 mmol), and the resulting mixture was stirred for 5 minutes, to which were added N-(3- dimethylammopropyl)~N -ethyl carbodiimide hydrochloride (26 mg, 0.132 mmol). The resulting mixture was stirred for 2 hours at room temperature, and then diluted with EtOAc. The organic layer was washed with IN HCl ₅ water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by chromatographyCHex/EtOAc^S/l) to give the title compound (28 mg, 80 %).

¹ H νMR(300MHz, CDCl ₃ ): δ 7.26 - 7.18 (m, 2H), 7.11 (s, IH), 4.66 - 4.60 (m, IH), 3.46 (s, 3H), 3.35 (s, 3H), 1.34 (d, 6H, J= 6.0 Hz).

Step 3: Synthesis of 3-(2-isopropoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester.

To a suspension of 2-isopropoxy-N~methoxy-N-methyl-4-trifluoromethyl~ benzamide (28 mg, 0.096 mmol) in THF (1.5 mL) was added dropwise 1.0M LiAlH ₄ (0.048 ml, 0.5 eq) at -6O ⁰ C. The mixture was slowly warmed up to -2O ⁰ C until the reaction was completed. The reaction was slowly quenched with sat'd KHSO ₄ (1 mL) and then diluted with water (1 mL). The reaction mixture was extracted with ether and the combined organic layer was dried over anhydrous MgSO _4; filtered and concentrated under reduced pressure. The resulting compound was vacuum dried to yield the 2-isopropoxy-4-trifluoromethyl- benzaldehyde. To the aldehyde prepared above was added toluene (1 mL) followed by portionwise addition of methyl (triρhenylphosphoranylidene)acetate (32 mg, 0.105 mmol) (exothermic). Toluene (1 mL) was added to the reaction mixture, and the resulting mixture was heated at 8O ⁰ C for 3 hours. The reaction mixture was cooled to room temperature, and then was directly loaded to a short silica-gel column and eluted with the solvent (Hex/EtOAc = 20/1) to give the title compound (20 mg, 72 %).

¹ H NMR(SOOMHZ, CDCl ₃ ): δ 7.96 (d, IH, J= 16.2 Hz), 7.58 (d, IH, J- 8.1 Hz), 7.17 (d, IH, J= 7.8 Hz), 7.11 (s, IH), 6.57 (d, IH, J= 16.2 Hz), 4.71 - 4.63 (m, IH) ₃ 3.81 (s, 3H), 1.41 (d, 6H, J= 6.3 Hz).

Step 4: Synthesis of N-ri-(3 _n 5-difluoro-4-methanesulfonylamino-phenyl)-ethyll- 3-(2-isopropoxy-4-trifluoromethyl-phenyl)-acrylamide.

To a suspension of 3-(2-isopropoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (15 mg, 0.052 mmol) in THF (1 ml) was added a solution of 0.5 N- LiOH (0.2 ml), and the resulting mixture was stirred for 3 hours at room temperature. The reaction mixture was acidified with IN HCl to pH 1~2. The mixture solution was extracted three times with methylene chloride, and the combined organic layer was dried over anhydrous Na ₂ SO ₄ and concentrated in vacuo to give 3-(2-isopiOpoxy-4-trifluoromethyl-phenyl)-acrylic acid (14 mg, 98 %). To a suspension of 3-(2-isopropoxy-4-trifluoromethyl-phenyl)-acrylic acid (14 mg, 0.051 mmol) and N-[4-(l-amino-ethyl)-2,6-difiuoro-phenyl]- methanesulfonamide, HCl salt (17.2 mg, 0.060 mmol) in DMF (2 mL) was added N-methylmorpholine (0.007 ml, 0.060 mmol). The mixture was stirred for 5 minutes, to which were added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (26 mg, 0.132 mmol). The mixture was stirred for 12 hours at room temperature, and then diluted with EtOAc (4 mL). The organic layer was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by chromatography (Hex/EtOAc = 1/1) to give the title compound (24 mg, 79 %). ¹ H νMR(300MHz, CDCl ₃ ): δ 7.93 (d, IH, J= 15.6 Hz), 7.56 (d, IH, J= 7.8 Hz), 7.16 (d, IH, J= 8.1 Hz), 7.10 (s, IH), 7.01 (d, IH, J= 8.4 Hz), 6.54 (d, IH, J = 15.6 Hz), 5.82 (d. IH ₅ J= 6.9 Hz), 5.19 (t, IH, J= 6.9 Hz), 4.67 - 4.63 (m, IH), 3.20 (s, 3H), 1.56 (d, 6H, J= 6.3 Hz). 1.40 (d, 3H, J= 5.4 Hz).

ESI [M-H]-; 505

Example 27: (KJ-N-[l-(3,5-Difluoro-4-methanesuIfonyIamino-phenyl)-ethyl] - 3-(4-fluoro-2-propoxy-ρhenyI)-acryIamide

Step 1: Synthesis of 3-(4-fluoro-2-hydroxy-phenyl)-acrylic acid methyl ester.

2-Hydroxy-4-fluoro-benzaldehyde (306 mg, 1.99 mmol) was reacted with methyl (triρhenylphosphoranylidene)acetate (681 g, 2.044 mmol) at 110 ⁰ C overnight as described above to yield title compound (334 mg, 85%).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.93 (d, IH, J = 15.9 Hz), 7.45 (m, IH) ₅ 6.65 (m,

IH), 6.59 (m, IH), 6.56 (s, IH), 6.53 (d, IH, J = 16.2 Hz), 5.27 (br, IH), 3.82 (s,

3H).

Step 2: Synthesis of 3-f4-flu.oiO-2-proρoxy-phenyl)-acrylic acid methyl ester

3-(4-Fluoro-2-hydroxy-phenyl)-acrylic acid methyl ester (110.5 mg) was reacted with K ₂ CO ₃ (111 mg) and propane iodide (0.1 ml) at 80 ⁰ C overnight as described above to yield title compound (134HIg, 100%)

¹ U NMR (300MHz, CDCl ₃ ): δ 7.90 (d, IH, J = 15.9 Hz), 7.45 (t, IH, J = 7.5 Hz), 6.65 (m, IH), 6.59 (m, IH), 6.49 (d, IH, J = 15.9 Hz) ₅ 3.96 (t, 2H, J = 6.6 Hz), 3.78 (s, 3H), 1.89 (m, 2H), 1.07 (t, 3H, J = 7.5 Hz).

Step 3: Synthesis of 3-(4-fluoro-2-propoxy-phenyl)-acrylic acid

3-(4-Fluoro-2-propoxy-ρhenyl)-acrylic acid methyl ester (134 mg, 0.563 mmol) was reacted with aqueous IN LiOH (5 ml) as described above to yield title compound (117 mg, 92%).

¹ H NMR (300MHz ₅ CDCl ₃ ): δ 8.00 (d, IH, J = 16.5 Hz), 7.49 (t, IH, J = 8.4 Hz), 6.67 (m, 2H) 6.50 (d, IH ₅ J = 15.9 Hz), 3.98 (t, 2H, J = 6.6 Hz) ₅ 1.91 (m, 2H) ₅ 1.09 (t, 3H, J = 7.2 Hz).

Step 4: Synthesis of ^gj-N-[l-(3,5-Difluoro-4-methanesulfoiiylamino-phenyl)- emyl]-3-f4-fluoro-2-propoχy-phenyl)-acrvlaniide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt (85 mg, 0.29 mmol) was reacted with 3-(4-fluoro-2-propoxy-phenyl)-acrylic acid (65 mg, 0.29 mmol), NMM (0.15 ml) and DMTMM (98 mg) at room temperature overnight to yield the title compound (77 mg, 58%) after column chromatography( Hex/EtOAc = 1/1).

¹ R NMR (300MHz ₅ CDCl ₃ ): δ 7.84 (d, IH, J = 15.6 Hz) ₅ 7.43 (t, IH ₅ J = 6.9 Hz) ₅ 6.98 (d, IH, J = 8.7 Hz), 6.63 (m, 2H), 6.47 (d, IH ₅ J = 15.6 Hz) ₅ 5.87 (br, IH), 5.18 (m, IH), 4.11 (t, 2H ₅ J = 6.9 Hz) ₅ 3.19 (s, 3H) ₅ 1.87 (m, 2H), 1.09 (t, 3H ₅ J = 7.5 Hz)

Example 28: N-(3,5-Difluoro-4-methanesulfonyIamino-benzyI)-3-(4-fluoro-2 - propoxy-phenyl)~acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide ₅ HCl salt

(66 mg, 0.24 mmol) was reacted with 3-(4-fϊuoro-2-propoxy-ρhenyl)-acrylic acid

(51 mg, 0.23 mmol), NMM (0.15 ml) and DMTMM (78 mg) at room temperature overnight to yield the title compound (52 mg, 0.12 mmol, 53%) after column chromatography( Hex/EtOAc = 1/1).

¹ U NMR (300MHz ₅ CDCl ₃ ): δ 7.90 (d, IH ₅ J = 15.9 Hz) ₅ 7.44 (t, IH, J = 6.6 Hz) ₅ 6.99 (d, IH ₅ J = 8.1 Hz), 6.65 (m, 2H), 6.52 (d, IH, J = 15.6 Hz) ₅ 5.89 (br, IH) ₅

4.55 (d, 2H ₅ J = 6.0 Hz), 3.98 (t, 2H, J = 6.6 Hz), 3.21 (s, 3H) ₅ 1.90 (m, 2H), 1.08

(t, 3H ₅ J = 7.5 Hz).

Example 29: fK)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)ethyI]- 3-(4-fluoro-2- propylaminophenyl)-acrylamide

Step 1. Synthesis of N-methoxy-N-methyl-4-fluoro-2-nitro-benzamide

To a solution of 4-fluoro-2-nitrobenzoic acid (1 g, 5.4 mmol), N ₃ O- dimethylhydroxylamine hydrochloride (0.58 g, 5.95 mmol) and N- methylmorpholine (0.65 mL, 5.91 mmol) in dichloromethane (20 mL) was added l-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.14 g, 5.95 mmol). The mixture was stirred for 80 minutes at room temperature. The mixture was concentrated under reduced pressure and then diluted with EtOAc and water. The organic layer was washed with 3 N HCl, saturated aqueous NaHCO ₃ solution and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give N-methoxy-N-methyl-4-fluoro-2-nitro-benzamide

(1.15 g, 95%).

¹ H NMR(300MHz, CDCl ₃ ): δ 7.89 ~ 7.85 (m, 1 H), 7.58 ~ 7.54 (m, 1 H), 7.47 ~ 7.41 (m, 1 H), 3.37 (s, 3 H), 3.36 (s, 3 H).

Step 2. Synthesis of N-methoxy-N-methyl-2-amino-4-fluoro-benzamide

A mixture of N-methoxy-N-methyl-4-fluoro-2-nitro-benzamide (1.15 g, 5.04 mmol) and 5% palladium charcoal (190 mg) in EtOH (30 mL) was shaken overnight under hydrogen atmosphere (3 atm). The mixture was filtered and concentrated under reduced pressure to give N-methoxy-N-methyl-2-amino-4- fluoro-benzamide (0.9 g, 90%). 1H NMR(SOOMHZ, CDCl ₃ ): δ 7.44 ~ 7.39 (m, 1 H), 6.40 ~ 6.30 (m, 2 H), 4.90 (bs,

2 H), 3.57 (s, 3 H), 3.34 (s, 3 H).

Step 3. Synthesis of N-methoxy-N-methyl-4-fluoro-2-propylamino-benzamide

To a solution of N-methoxy-N-methyl-2-amino-4-fluoro-benzamide (0.27 g, 1.36 mmol), propionaldehyde (0.15 mL, 2.08 mmol), and AcOH (0.12 mL, 2.1 mmol) in dichloromethane (20 mL) was added sodium triacetoxyborohydride (576 mg, 2.72 mmol) at 5 ⁰ C. The mixture was stirred for 90 minutes at the same temperature and then 40 minutes at room temperature. The reaction was quenched by adding water. The organic layer was washed with saturated aqueous NaHCO ₃ solution and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give N-methoxy-N-methyl-4-fiuoro-2- propylamino-benzamide quantitatively. 1H NMR(300MHz, CDCl ₃ ): δ 7.40 (t, 1 H, J= 7.2 Hz), 6.34 ~ 6.25 (m, 2 H), 3.58 (s, 3 H), 3.33 (s, 3 H), 3.03 (t, 2 H, J= 6.9 Hz), 1.72 ~ 1.59 (m, 2 H), 1.00 (t, 3 H, J= 7.2 Hz).

Step 4. Synthesis of 3-(4-fluoro-2-propylamino-phenyl)-acrylic acid methyl ester

To a solution of N-methoxy-N-methyl-4-fluoro-2-propylamino-benzamide

(0.33 g, 1.37 mmol) in THF (4 mL) was added dropwise LiAlH ₄ (1 M in THF, 0.7 mL) at -45 ⁰ C. The mixture was stirred for 40 minutes at -35 ⁰ C and then quenched by adding saturated aqueous KHSO ₄ solution. The mixture was diluted with EtOAc, washed with 3 N HCl, and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was reacted with methyl (triphenylphosphoranylidene)acetate (0.5 g, 1.5 mmol) in toluene (4 mL) overnight at 100 ⁰ C. The mixture was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (0.23 g, 69%) after purification by column chromatography (EtOAc : hexane = 1 : 10).

¹ H NMR(300MHz, CDCl ₃ ): δ 7.72 (d, 1 H, J = 15.6 Hz), 7.34 ~ 7.29 (m, 1 H),

6.41 ~ 6.29 (m, 2 H), 6.27 (d, 1 H, J= 15.6 Hz), 4.16 (bs, 1 H), 3.80 (s, 3 H), 3.12

~ 3.07 (m, 2 H), 1.76 ~ 1.63 (m, 2 H), 1.02 (t, 3 H, J= 7.2 Hz).

Step 5. Synthesis of (R)-N-[I -(3, 5-difluoro-4-methanesulfonylaminophenyl) ethyll-3-(4-fluoro-2-propylamino-phenyl)-acrylamide

To a solution of 3-(4-fluoro-2-propylamino-phenyl)-acrylic acid methyl ester (0.23 g, 0.95 mmol) in THF (4 mL) and MeOH (2 mL) was added 1 N LiOH (4 mL). The mixture was stirred for 2 hours at room temperature, concentrated under reduced pressure, and then acidified with 3 N HCl. The mixture was diluted with EtOAc, washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give 3-(4-fluoro-2-propylamino- phenyl)-acrylic acid (0.17 g, 79%) after purification by crystallization form EtOAc and hexane. To a mixture of 3-(4-fluoro-2-propylamino-phenyl)-acrylic acid (50 mg, 0.22 mmol), (R)-[l-(3,5-difluoro-4-methanesulfonylamino phenyl)ethylamine hydrochloride (64 mg, 0.22 mmol) and N-methylmorpholine (36 μL _s 0.33 mmol) in THF (5 mL) was added 4-(4,6-dimethoxy[l,3,5]triazin-2- yl)-4-methylmorpholirium chloride hydrate (DMTMM, 68 mg, 0.25 mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was diluted with EtOAc and water, and the aqueous layer was washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (35 mg, 34%) after purification by crystallization form EtOAc and hexane, 1H NMR(300MHz, CDCl ₃ ): δ 7.78 (d, 1 H, J= 15 Hz), 7.32 ~ 7.26 (m, 1 H), 6.93 (d, 2 H ₅ J= 8.4 Hz), 6.78 (s, 1 H), 6.37 ~ 6.29 (m, 2 H), 6.22 (d, 1 H, J= 15 Hz), 5.87 (d, 1 H, J= 6.9 Hz), 5.13 (t, 1 H, J= 6.9 Hz), 4.48 (bs, 1 H), 3.18 (s, 3 H), 3.08 (t, 2 H, J= 6.9 Hz), 1.71 ~ 1.58 (m, 2 H), 1.49 (d, 3 H, J= 6.9 Hz), 0.99 (t, 3 H, J= 7.2 Hz).

Example 30: N-[l-(3,5-Difluoro-4-methanesuIfonyIaminobenzyl]-3-(4- fluoro-2-«-propylamino-phenyl)-acrylamide

To a mixture of 3-(4-fluoro-2-propylamino-phenyl)-acrylic acid (50 mg,

0.22 mmol), (3,5-difluoro-4-methanesulfonylamino)benzylamine hydrochloride (61 mg, 0.22 mmol) and N-methylmorpholine (36 μL, 0.33 mmol) in THF (5 mL) was added 4-(4,6-dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholirium chloride hydrate (DMTMM, 68 mg, 0.25 mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was diluted with EtOAc and water, and the aqueous layer was washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (9 mg, 9%) after purification by column chromatography (EtOAc : hexane = 1 : 1). 1H NMR(300MHz, CDCl ₃ ): δ 7.60 (d, 1 H ₅ J= 15 Hz), 7.32 ~ 7.26 (m, 1 H), 6.96 (d, 2 H, J = 8.1 Hz), 6.93 ~ 6.32 (m, 2 H), 6.14 (d, 1 H, J= 15 Hz), 6.13 (br, 1 H), 5.95 (br, 1 H), 4.53 (d, 2 H, J = 5.7 Hz), 4.25 (br, 1 H), 3.21 (s, 3 H), 3.09 (m, 2 H), 1.72 ~ 1.65 (m, 2 H), 1.01 (t, 3 H, J= 7.2 Hz).

Example 31: fi2>3-(2-Butoxy-4-trifluoromethyl-phenyl)-N-[l-(3,5-diflu oro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

Step 1 : Synthesis of 2-butoxy-4-trifluoromethyl-benzoic acid butyl ester

2-Hydroxy-4-trifluoromethyl-benzoic acid (755 mg) was reacted with

butylbromide (0.96 ml) and K ₂ CO ₃ (1.15 g) in DMF solution as described above to yield title compound.

¹ H NMR (300MHz, CDCl ₃ ): δ 8.01 (s, IH), 7.801 (d, IH, J = 7.8 Hz), 7.19 (m, 2H), 4.32 (t, 2H, J = 6.6 Hz), 4.06 (t, 2H, J = 6.3 Hz), 1.82 (m, 2H), 1.75 (m, 2H), 0.98 (m, 6H)

Step 2: Synthesis of 2-butoxy-4-trifluoromethyl-benzoic acid

2-Butoxy-4-trifluoromethyl-benzoic acid butyl ester was reacted with IN LiOH (10 ml) as described above to yield title compound (687 mg).

¹ H NMR (300MHz, CDCl ₃ ): δ 8.29 (d, IH, J = 8.4 Hz), 7.38 (d, IH, J = 8.1 Hz), 4.31 (t, 2H, J = 6.3 Hz), 1.94 (m, 2H), 1.53 (m, 2H), 1.02 (t, 3H, J = 7.5 Hz)

Step 3: Synthesis of 2-butoxy-N-methoxy-N-methyl-4-trifluoromethyl-benzamide

2-Butoxy-4-trifluoromethyl-benzoic acid (687 mg) was reacted with N ₅ O- dimethylhydroxy amine (331 mg), NMM (0.65 ml) and DMTMM (911 mg) as described above to yield the title compound (825 mg) after column chromatography (Hex/EtOAc = 7.5/1). 1H NMR (300MHz, CDCl ₃ ): δ 7.36 (br, IH), 7.22 (d, IH, J = 8.1 Hz), 7.11 (s, IH),

4.04 (t, 2H, J = 6.3 Hz), 3.45 (s, 3H), 3.35 (s, 3H), 1.77 (m, 2H), 1.46 (m, 2H),

0.99 (t, 3H, J = 7.5 Hz)

Step 4: Synthesis of 2-butoxy-4-trifluoromethyl-benzaldehvde

2-Butoxy-N-methoxy-N-methyl-4-trifluoromethyl-benzamide (825 mg) was reacted with 1 M LAH (31 ml) at -50 ⁰ C for 1 hour as described above to yield title compound (423 mg) after column chromatography (Hex/EtOAc = 20/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 10.53 (s, IH), 7.92 (d, IH, J = 7.8 Hz), 7.27 (d, IH, J = 8.7 Hz), 7.21 (s, IH), 4.10 (t, 2H, J = 6.3 Hz), 1.89 (m, 2H) ₅ 1.57 (m, 2H),

1.01 (t, 3H, J = 7.2 Hz)

Step 5: Synthesis of 3-r2-butoxy-4-trifluoromethyl-phenylVacrylic acid methyl ester

2-Butoxy-4-trifluoromethyl-benzaldehyde (420 mg) was reacted with methyl (triphenylphosphoranylidene)acetate (679 mg) at 110 ⁰ C overnight as described above to yield title compound (464 mg) after column chromatography (Hex/EtOAc = 20/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.91 (d, IH ₅ J = 16.5 Hz), 7.53 (d, IH, J = 7.8 Hz), 7.13 (m, IH), 7.06 (s, IH), 6.54 (d, IH, J = 16.2 Hz), 4.03 (t, 2H, J = 6.6 Hz), 3.77 (s, 3H), 1.82 (m, 2H), 1.48 (m, 2H), 0.96 (t, 3H, J = 7.5 Hz)

Step 6: Synthesis of 3-(2-butoxy-4-trifluoromethyl-phenyl)-acrylic acid

3-(2-Butoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester (464 mg) was reacted with IN LiOH (10 ml) in THF and CH ₃ OH for 1 hr as described above to yield title compound

¹ H NMR (300MHz, CDCl ₃ ): δ 8.05 (d, IH, J = 16.2 Hz), 7.60 (d, IH, J = 8.1 Hz), 7.20 (m, IH), 7.12 (s, IH), 6.62 (d, IH, J = 16.2 Hz), 4.09 (t, 2H, J = 6.0 Hz), 1.85 (m, 2H), 1.56 (m, 2H), 1.04 (t, 3H, J = 7.5 Hz)

Step 7: Synthesis of (RJ-3-(2-butoxy-4-trifluoromethyl-phenylVN-ri-(3,5- difluoro-4-methanesulfonylamino-phenyl)-ethyl]-acrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt (75 mg, 0.26 mmol) was reacted with 3-(2-butoxy-4-trifluoromethyl-phenyl)- acrylic acid (63 mg, 0.230 mmol), NMM (0.15 ml) and DMTMM (75 mg) at room temperature overnight to yield the title compound (52 mg, 0.10 mmol, 43%) after column chromatography^ Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.93 (d, IH, J = 15.6 Hz), 7.55 (d, IH, J = 7.8 Hz), 7.18 (d, IH ₅ J = 8.1 Hz), 6.99 (d, IH, J = 6.6 Hz), 6.75 (d, IH ₅ J = 8.4 Hz) ₅ 6.52 (d,

IH, J = 15.6 Hz) ₅ 5.89 (br, IH), 5.18 (t, IH), 4.10 (d, 2H, J = 6.0 Hz), 3.19 (s, 3H) ₅

1.87 (m, 2H) ₅ 1.52 (m, 2H), 0.99 (t, 3H ₅ J = 7.2 Hz).

ESI [M-H]--. 519

Example 32: 3-(2-Butoxy-4-trifluoromethyl-phenyl)-N-(3,5-difluoro-4- methanesulfonylamino-benzyl)-acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt (65 mg, 0.24 mmol) was reacted with 3-(2-butoxy-4-trifluoromethyl-phenyl)- acrylic acid (57 mg, 0.20 mmol), NMM (0.2 ml) and DMTMM (66 mg) to give the title compound (62 mg, 012 mmol, 62%) after column chromatography ( Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.96 (d, IH, J = 15.6 Hz), 7.56 (d, IH, J = 8.1 Hz), 7.20 (d, IH, J = 7.2 Hz), 7.11 (s, IH), 6.99 (d, IH ₅ J = 8.1 Hz), 6.75 (d, IH, J = 8.1 Hz), 6.52 (d, IH, J = 15.6 Hz), 6.05 (br, IH), 4.55 (d, 2H, J = 6.3 Hz), 4.10 (d, 2H, J = 6.9 Hz), 3.20 (s, 3H), 1.88 (m, 2H), 1.57 (m, 2H), 0.98 (t, 3H, J = 7.2 Hz).

Example 33 : (#>3-(2-Butoxy-4-fluoro-phenyl)-N-[l-(3,5-diflιioro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

Step 1: Synthesis of 3-(2-butoxy-4-fluoro-phenyl)-acrylic acid methyl ester

3-(4-Fluoro-2-hydroxy-phenyl)-acrylic acid methyl ester (106 mg) was reacted with K ₂ CO ₃ (125 mg) and butyl iodide (0.1 ml) at 80 ⁰ C for 3 hrs as described above to yield title compound (121 mg).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.90 (d, IH, J = 16.2 Hz), 7.45 (m, IH), 6.64 (m,

2H), 6.47 (d, IH, J = 15.9 Hz), 4.00 (t, 2H ₅ J = 6.6 Hz), 3.79 (s, 3H), 1.84 (m, 2H) ₅ 1.53 (m, 2H) ₅ 0.99 (t, 3H, J = 7.2 Hz)

Step 2: Synthesis of 3-f2-butoxy-4-fruoro-phenyl)-acrylic acid

3-(2-Butoxy-4-fluoro-phenyl)-acrylic acid methyl ester (121 mg) was reacted with IN LiOH (5ml) in THF and CH ₃ OH for 2 hrs as described above to yield title compound (116 mg).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.99 (d, IH, J - 16.2 Hz), 7.48 (m, IH), 6.65 (m, 2H), 6.49 (d, IH ₅ J = 16.2 Hz), 4.02 (t, 2H, J = 6.3 Hz) ₅ 1.86 (m, 2H), 1.54 (m, 2H), 1.00 (t, 3H ₅ J = 7.2 Hz).

Step 3: Synthesis of ^)-3-f2-butoχy-4-fluoro-ρhenyl)-N-[l-f3,5-difluoro-4- methanesulfonylamino-phenvD-ethvll-acrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt (75 mg, 0.26 mmol) was reacted with 3-(2-butoxy-4-fluoro-phenyl)-acryIic acid (60 mg, 0.25 mmol), NMM (0.15 ml) and DMTMM (82 mg) at room temperature overnight to yield the title compound (87 mg ₅ 0.19 mmol, 74%) after column chromatography (Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.85 (d, IH, J = 15.9 Hz), 7.42 (m, IH) ₅ 6.94 (d, 2H, J - 8.4 Hz), 6.62 (m, 2H), 6.47 (d, IH, J = 15.6 Hz), 6.23 (d, IH ₅ J = 7.2 Hz), 5.13 (t, IH), 4.11 (t, 2H, J = 6.3 Hz) ₅ 3.17 (s, 3H) ₅ 1.81 (m, 2H), 1.54 (m, 2H) ₅ 1.46 (d, 3H, J = 6,6 Hz) ₅ 0.90 (t, 3H ₅ J = 7.2 Hz). ESI [M-H] ^" : 469

Example 34: 3-(2-Butoxy-4-fluoro-phenyl)-N-(3,5-difluoro-4- methanesulfonylamino-benzyty-acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt

(73 mg, 0.26 mmol) was reacted with 3-(4-fluoro-2-propoxy-phenyl)-acrylic acid

(55 mg, 0.23 mmol), NMM (0.15 ml) and DMTMM (73 mg) at room temperature overnight to yield the title compound (85 mg, 0.19 mmol, 81%) after column chromatography^ Hex/EtOAc = 1/1).

¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.89 (d, IH, J = 15.6 Hz), 7.45 (m, IH), 6.94 (d, 2H, J = 8.4 Hz), 6.98 (m, IH), 6.64 (m, IH), 6.50 (d, IH, J = 15.6 Hz) ₃ 6.07 (br, IH), 4.55 (d, 2H, J = 6.0 Hz), 4.13 (t, 2H, J = 6.3 Hz), 3.20 (s, 3H) ₅ 1.83 (m, 2H), 1.52 (m, 2H), 0.88 (t, 3H, J = 7.2 Hz).

Example 35: N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-(2- propyl-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2-ethynyl-6-fluoro-phenyl)-methanesulfonami de, HCl salt (14mg, 0.050mmol) was reacted with 3-(2-propyl-4-trifluoromethyl-ρhenyl)- acrylic acid (8mg, 0.031mmol) to give the title compound (12mg, 80%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex). ¹ H NMR(300MHz, DMSO-d ⁶ ): δ 8.79 (t, IH), 7.69 (m, 4H), 7.74 (m, 2H), 7.60 (m, 2H), 7.26 (m, 2H), 6.72 (d, IH, J= 15.6 Hz), 4.45 (s, IH), 4.38 (d, IH, J= 5.4 Hz), 3.01 (s, 3H), 2.70 (t, 2H, J = 7.5 Hz), 1.54 (m, 2 H), 1.23 (m, 2 H), 0.91 (m, 3H). ESI [M+H] ⁺ :

Example 36: (i?)-3-(2-ButyI-4-trifluoromethyI-phenyI)-N-[l-(3-fluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

(R)-N-[4-(l-Amino-ethyl)-2-fluoro-phenyl]-methanesulfonam ide, HCl salt

(20mg, 0.074mmol) was reacted with 3-(2-butyl-4-trifluoromethyl-phenyl)- acrylic acid (8mg, 0.031mmol) to give the title compound (5mg, 35%) after purification by column chromatography (gradient 12% to 100% EtOAc in Hex). 1H NMR(300MHz, DMSO-d ⁶ ): δ 8.66 (d, IH, J= 8.1 Hz), 7.66 (m, 3H) ₅ 7.51 (bs, 2H), 7.31 (t, IH, J= 8.4 Hz), 7.17 (d, IH, J= 11.4 Hz), 7.09 (d, IH, J= 8.1 Hz), 6.70 (d, IH, J = 15.6 Hz), 5.00 (m, IH), 2.91 (s, 3H), 2.78 (t, 2H, J = 7.8 Hz), 1.47 (m, 2 H), 1.40 (d, 3H, J= 12 Hz), 1.32 (m, 2 H), 0.89 (t, 3H, J= 7.2 Hz). ESI [M-H]-; 485

Example 37: N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-propyl]-3- (2-ethoxy-4-trifluoromethyl-phenyl)-acrylamide

To a suspension of 3-(2-ethoxy-4-trifluoromethyl-phenyl)-acrylic acid (39 mg, 0.151 mmol) and N-[4-(l-amino-propyl)-2,6-difluoro-phenyl]- methanesulfonamide, HCl salt (50 mg, 0.166 mmol) in DMF (2 mL) was added

N-methylmorpholine (0.02 ml, 0.018 mmol). The mixture was stirred for 5 minutes, to which were added N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (33 mg, 0.166 mmol). The mixture was stirred for 12 hours at room temperature, and then diluted with EtOAc (4 mL). The organic layer was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by

chromatography (Hex/EtOAc = 1/1) to give the title compound. (43 mg, 51 %). ¹ H NMR(300MHz, DMSO-d ⁶ ): δ 9.50 (bs, IH), 8.65 (d, IH, J= 7.8 Hz) ₅ 7.74 (d, IH ₅ J= 7.8 Hz) ₅ 7.67 (d ₅ IH ₅ J= 15.9 Hz), 7.33 (d, IH ₅ J= 8.1 Hz) ₅ 7.31 (s, IH), 7.15 (d, IH ₅ J= 8.7 Hz), 6.82 (d, IH, J= 15.9 Hz) ₅ 4.87 - 4.80 (m, IH), 4.19 (q, 2H ₅ J= 6.9 Hz), 3.04 (s, 3H), 1.75 - 1.70 (m, 2H), 1.39 (t, 3H, J= 6.9 Hz). 0.88 (t, 3H, J= 6.9 Hz).

Example 38: 3-(2-Butoxy-4-trifluororaethyl-phenyl)-N-[l-(3,5-difluoro-4- methanesulfonylamino-phenyl)-propyl]~acrylamide

N-[4-( 1 -Amino-propyl)-2,6-difluoro-phenyl]-methanesulfonamide ₅ HCl salt (50 mg, 0.166 mmol) was reacted with 3-(2-butoxy-4-trifluoromethyl- phenyl)-acrylic acid (43.5 mg, 0.151 mmol) to give the title compound (43 mg, 54 %) after purification by column chromatography.

¹ H NMR(300MHz, DMSO-d ⁶ ): δ 9.47 (bs, IH) ₅ 8.65 (d, 2H, J= 8.1 Hz) ₅ 7.73 (d, IH, J= 8.4 Hz), 7.68 (d, IH ₅ J= 16.2 Hz), 7.33 (s, IH), 7.15 (d, 2H, J= 8.7 Hz), 6.80 (d, IH ₅ J= 16.2 Hz) ₅ 4.82 (q, IH, J= 7.2 Hz), 4.12 (d, 2H, J= 6.3 Hz), 3.04 (s, 3H), 1.83 - 1.67 (m, 4H), 1.51 - 1.41 (m, 2H) ₅ 0.96 - 0.86 (m, 6H).

Example 39: (λ)-3-(2-sec-Butoxy-4-trifluoromethyl-phenyl)>N-[l-(3,5- difluoro-4-methanesuIfonyIamino-phenyl)-ethyl]-acrylamide

. „ 2009/096701

Step 1: Synthesis of 2-sec-butoxy-N-methoχy-N-methvl-44rifluoromethyl- benzamide

A mixture of 2-hydroxy-4-trifluoromethyl-benzoic acid (300 mg, 1.45 mmol) in DMF was added potassium carbonate (442 mg, 3.20 mmol) followed by 2-iodobutane (589 mg, 3.2 mmol). The mixture was stirred for 48 hours at 110 ⁰ C and then diluted with EtOAc. The organic layer was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was dissolved in THF (2 ml) and then added a solution of 0.5 N-LiOH (2 eq). The mixture was stirred for 2 hours at room temperature and then diluted with EtOAc. The organic layer was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue and N,O- dimethylhydroxylamine hydrochloride (316 mg, 0.16 mmol) in CH ₂ Cl ₂ (5 mL) was added N-methylmorpholine (0.176 ml, 0.160 mmol). The mixture was stirred for 5 minutes, to which were added N-(3-dimethylaminopropyl)-N'- ethylcarbodiimide hydrochloride (316 mg, 0.160 mmol). The mixture was stirred for 2 hours at room temperature and then diluted with EtOAc. The organic layer was washed with IN HCl, water, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by chromatography to give the title compound. (374 mg, 84 %). 1H NMR(300MHz ₅ CDCl ₃ ): δ 7.23 - 7.19 (m, 2H), 7.09 (s, IH), 4.40 - 4.37 (m, IH), 3.42 (s, 3H), 3.34 (s, 3H), 1.77 - 1.67 (m, 2H), 1.30 (d, 3H, J= 3.0 Hz), 0.97 (t, 3H, J= 7.2 Hz).

Step 2: Synthesis of 3-r2-sec-butoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester

2-sec-Butoxy-N-methoxy-N-methyl-4-trifluoromethyl-benzami de (130 mg, 0.425 mmol) was processed with reduction and wittig reaction as described above to give the title compound (100 mg, 61 %) after purification by column chromatography.

¹ H NMR(300MHz, CDCl ₃ ): 7.97 (d, IH, J = 16.2 Hz), 7.58 (d, IH ₅ J = 7.8 Hz), 7.17 (d ₅ IH, J= 7.8 Hz) ₅ 7.09 (s, IH) ₅ 6.57 (d, IH, J= 16.2 Hz), 4.48 - 4.42 (m, IH), 3.81 (s, 3H), 1.86 - 1.69 (m, 2H) ₅ 1.35 (d, 3H ₅ J= 6.0 Hz), 1.01 (t, 3H ₅ J = 7.2 Hz).

Step 3: Synthesis of 3-(2-sec-butoxy-4-trifluoromethyl-phenyl)-N-ri-(3,5- difluoro-4-methanesulfonylamino-phenyl)-ethyl]-acrylamide

N- [4-( 1 - Amino-ethy l)-2,6-difluoro-phenyl]-methanesulfonamide, HCl salt (17.7 mg, 0.062 mmol) was reacted with 3-(2-sec-butoxy-4-trifluoiOmethyl- phenyl)-acrylic acid (16.2 mg, 0.056 mmol) to give the title compound (15 mg,

52 %) after purification by column chromatography.

¹ B. NMR(300MHz, CDCl ₃ ): δ 7.93 (d, IH ₅ J= 15.9 Hz) ₅ 7.56 (d, IH ₅ J= 8.1 Hz) ₅

7.11 (d ₅ IH, J = 8.1 Hz), 7.09 (s, IH), 6.99 (d, 2H, J = 8.1 Hz), 6.53 (d, IH, J = 15.9 Hz) ₅ 5.96 (d, IH, J= 7.2 Hz), 5.23 - 5.14 (m, IH), 4.43 (q, IH ₅ J= 6.0 Hz),

3.19 (s, 3H) ₅ 1.86 - 1.77 (m, IH) ₅ 1.73 - 1.62 (m, IH) ₅ 1.52 (d, 3H, J = 6.9 Hz),

1.33 (d, 3H ₅ J= 6.0 Hz) ₅ 0.99 (t, 3H ₅ J= 7.2 Hz).

ESI [M-H] ^" : 519

Example 40: (i?)-3-(2-sec-Butoxy-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

Step 1 : Synthesis of 3-(2-sec-butoxy-4-fluoro-phenyl)-acrylic acid methyl ester

3-(4-Fluoro-2-hydroxy-phenyl)-acrylic acid methyl ester (120 mg) was reacted with K ₂ CO ₃ (165 mg) and 2-iodobutan (0.12 ml) at 100 ⁰ C for 3 hrs as described above to yield title compound (105 mg)

¹ H NMR (300MHz, CDCl ₃ ): δ 7.90 (d, IH, J = 15.9 Hz) ₅ 7.45 (m ₅ IH) ₅ 6.63 (m,

2H), 6.45 (d, IH ₅ J = 15.9 Hz) ₅ 4.33 (m, IH ₅ J = 6.0 Hz) ₅ 3.79 (s, 3H) ₅ 1.82 (m, IH) ₅ 1.71 (m, IH) ₅ 1.33 (d, 2H ₅ J = 6.0 Hz) ₅ 0.99 (t, 3H ₅ J = 7.2 Hz)

Step 2: Synthesis of 3-f2-sec-butoxy-4-fluoro-phenyl)-acrylic acid

3-(2-sec-Butoxy-4-fluoro-ρhenyl)-acrylic acid methyl ester (105 mg) was reacted with IN LiOH (5 ml) in THF and CH ₃ OH for 2 hrs as described above to yield title compound (82 mg)

¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.97 (d, IH ₅ J = 16.2 Hz) ₅ 7.50 (m, IH) ₅ 6.62 (m ₅ 2H), 6.47 (d, IH ₉ J = 16.2 Hz), 4.02 (m, IH, J = 6.0 Hz) ₅ 1.86 (m, IH), 1.73 (m, IH) ₅ 1.34(d, 3H) ₅ 1.00 (t, 3H, J = 7.2 Hz).

Step 3: Synthesis of rRJ-3-(2-sec-butoxy-4-fluoro-phenvD-N-ri-(3,5-difluoro-4- methanesulfonylamino-phenyl)-ethyl]-acrylamide

(R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonami de, HCl salt (69 mg, 0.24 mmol) was reacted with 3-(2-sec-butoxy-4-fluoro-phenyl)-acrylic acid (55 mg, 0.23 mmol), NMM (0.15 ml) and DMTMM (75 mg) at room temperature overnight to yield the title compound (15 mg, 14%) after column chromatography (Hex/EtOAc = 1/1).

¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.87 (d, IH ₅ J = 15.6 Hz) ₅ 7.43 (m, IH), 6.99 (d, IH ₅ J = 8.7 Hz) ₅ 6.64 (m, 2H), 6.41 (d, IH, J = 15.6 Hz) ₅ 6.11 (s, IH) ₅ 5.80 (d, IH ₅ J= 7.5 Hz) ₅ 5.17 (t, IH) ₅ 4.33 (m, IH, J = 6.0 Hz) ₅ 3.19 (s, 3H) ₅ 1.78 (m, IH), 1.67 (m, IH), 1.49 (d, 3H, J = 7.2 Hz), 1.32 (d, 3H, J = 6.0 Hz), 0.98 (t, 3H, J = 7.2 Hz). ESI [M-H] ^' : 469

Example 41: 3-(2-sec-Butoxy-4-fluoro-phenyI)-N-(3,5-difluoro-4- methanesulfonylamino-benzyl)-acrylamide

N-(4-Aminomethyl-2,6-difluoro-phenyl)-methanesulfonamide, HCl salt

(42 mg, 0.15 lnmol) was reacted with 3-(4-fluoro-2-propoxy-phenyl)-acrylic acid

(34 mg, 0.14 mmol), NMM (0.15 ml) and DMTMM (43 mg) at room temperature overnight to yield the title compound (15 mg, 23%) after column chromatography^ Hex/EtOAc = 1/1).

¹ H NMR (300MHz, CDCl ₃ ): δ 7.89 (d, IH ₅ J = 15.9 Hz), 7.44 (m, IH), 6.97 (d, IH, J = 8.4 Hz), 6.65 (s, IH), 6.60 (d, IH, J = 9.3 Hz), 6.47 (d, IH, J = 15.6 Hz), 6.08 (s, IH), 6.00 (s, IH, J= 7.5 Hz), 4.53 (d, 2H, J = 6.0 Hz), 4.34 (m, IH, J = 6.0 Hz), 3.20 (s, 3H), 1.78 (m, IH), 1.67 (m, IH), 1.49 (d, 3H, J = 7.2 Hz), 1.34 (d, 3H ₅ J = 6.0 Hz), 0.99 (t, 3H, J = 7.2 Hz).

Example 42: fK)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl] - 3-(2-ethylamino-4-fluoro-phenyl)-acrylamide

Step 1: Synthesis ofN-methoxy-N-methyl-4-fluoro-2-ethylamino-benzamide

To a solution of N-methoxy-N-methyl-2-amino-4-fluoro-benzamide (0.20 g, 1.01 mmol), acetaldehyde (86 μL, 1.53 mmol), and AcOH (87 μL, 2.1 mmol) in dichloromethane (20 mL) was added sodium triacetoxyborohydride (430 mg, 2.03 mmol) at 5 ⁰ C. The mixture was stirred for 90 minutes at the same temperature and then 40 minutes at room temperature. The reaction was quenched by adding water. The organic layer was washed with saturated aqueous NaHCO ₃ solution and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give N-methoxy-N-methyl-4-fluoro-2-ethylamino-benzamide quantitatively.

¹ H NMR(300MHz, CDCl ₃ ): δ 7.43 ~ 7.38 (m, 1 H) ₅ 6.35 ~ 6.25 (m, 2 H), 3.58 (s, 3 H), 3.33 (s, 3 H), 3.16 - 3.07 (m, 2 H), 1.27 (t, 3 H, J= 6.9 Hz).

Step 2: Synthesis of 3-(4-fluoro-2-ethylamino-phenylVacrylic acid methyl ester

To a solution of N-methoxy-N-methyl-4-fluoro-2-ethylamino-benzamide (0.23 g, 1.02 mmol) in THF (4 mL) was added dropwise LiAlH ₄ (1 M in THF, 0.51 mL) at -45 ⁰ C. The mixture was stirred for 40 minutes at -35 ⁰ C and then quenched by adding saturated aqueous KHSO ₄ solution. The mixture was diluted with EtOAc, washed with 3 N HCl, and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was reacted with methyl (triphenylphosphoranylidene)acetate (375 mg, 1.12 mmol) in toluene (4 mL) overnight at 100 ⁰ C. The mixture was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (0.13 g, 57%) after purification by column chromatography (EtOAc : hexane = 1 : 10). 1H NMR(300MHz, CDCl ₃ ): δ 7.73 (d, 1 H, J= 15.6 Hz), 7.32 (t, 1 H ₃ J= 7.2 Hz), 6.42 ~ 6.32 (m, 2 H), 6.27 (d, 1 H, J= 15.6 Hz), 4.09 (br, 1 H), 3.80 (s, 3 H), 3.19 ~ 3.15 (m, 2 H), 1.31 (t, 3 H ₅ J= 7.2 Hz).

Step 3: Synthesis of CR)-N-Tl -(3, 5-Difluoro-4-methanesulfonylaminophenyl) ethyl]-3-(4-fluoro-2-ethylaminophenyl)acrylamide

To a solution of 3-(4-fluoro-2-ethylamino-phenyl)-acrylic acid methyl ester (128 mg, 0.57 mmol) in THF (4 mL) and MeOH (2 mL) was added 1 N LiOH (4 mL). The mixture was stirred for 2 hours at room temperature, concentrated under reduced pressure, and then acidified with 3 N HCl. The mixture was diluted with EtOAc, washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give 3-(4- fluoro-2-ethylamino-phenyl)-acrylic acid (88 mg, 73%) after purification by crystallization form EtOAc and hexane. To a mixture of 3-(4-fluoro-2- ethylamino-phenyl)-acrylic acid (40 mg, 0.19 mmol), (R)-[l-(3,5-difluoro-4- methanesulfonylaminophenyl)-ethylamine hydrochloride (55 mg, 0.19 mmol) and N-methylmorpholine (31 μL, 0.28 mmol) in THF (4 mL) was added 4-(4,6- dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholirium chloride hydrate (DMTMM,

58 mg, 0.21 mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was diluted with EtOAc and water, washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (4.9 mg, 6%) after purification by column chromatography (EtOAc : hexane = 1 : 10 to 2:1).

¹ H NMR(300MHz, CDCl ₃ + DMSO-d6): δ 9.05 (br, 1 H), 8.00 (d, 1 H, J = 7.8 Hz), 7.62 (d, 1 H, J = 15.3 Hz), 7.29 (t, 1 H, J= 7.8 Hz), 7.01 (d, 2 H, J= 8.4 Hz), 6.40 (d, 1 H, J= 15.3 Hz), 6.37 ~ 6.28 (m, 2 H) ₅ 5.13 (t, 1 H, J= 6.9 Hz), 4.50 (bs, 1 H), 3.20 ~ 3.10 (m, 2 H), 3.08 (s, 3 H), 1.48 (d, 3 H, J= 6.9 Hz), 1.28 (t, 3 H, J = 7.2 Hz). ESI [M-H]-; 440

Example 43 : N-(3,5-Difluoro-4-methanesulfonylaminobenzyl)-3-(4-fluoro- 2-ethylaminophenyl)acrylamide

To a mixture of 4-fluoro-2-ethylaminocinnamic acid (40 mg, 0.19 mmol), (3,5-difluoro-4-methanesulfonylamino)benzylamine hydrochloride (52 mg, 0.19 mmol) and N-methylmorpholine (31 μL, 0.28 mmol) in THF (4 mL) was added 4- (4,6-dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholirium chloride hydrate (DMTMM, 58 mg, 0.21 mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was diluted with EtOAc and water, and the organic layer was washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (17 mg, 21%) after trituration with ethyl ether.

¹ H NMR(SOOMHZ, CDCl ₃ + DMSO-d6): δ 9.07 (bs, 1 H), 8.14 (br, 1 H), 7.66 (d, 1 H, J= 15.6 Hz), 7.31 (t, 1 H, J= 7.2 Hz), 6.98 (d, 2 H, J= 8.1 Hz), 6.40 (d, 1 H, J= 15.3 Hz), 6.37 ~ 6.29(m, 2 H), 4.55 (br, 1 H), 4.47 (d, 2 H, J= 5.7 Hz), 3.18 ~

3.12 (m, 2 H), 3.09 (s, 3 H), 1.29 (t, 3 H, /= 7.2 Hz).

Example 44: (ϋJ)-N-(2-Fluoro-4-{l-[3-(2-propyl-4-trifluoromethyl-phenyl )- allylamino]-ethyl}-phenyl)-methanesulfonamide

(R)-N- [4-( 1 -Amino-ethyl)-2-fluoro-phenyl]-methanesulfonamide, HCl salt (31mg, 0.12mmol) was reacted with 3-(2-ρropyl-4-trifluoromethyl-phenyl)- acrylic acid (25mg, 0.097mmol) to give the title compound (32mg, 70%) after purification by recrystallization from Hex/EtOAc.

¹ H NMR(300MHz, DMSO-d6): δ 8.70 (d, IH, J= 7.5 Hz), 7.66 (m, 3H), 7.33 (t, IH, J= 8.1 Hz), 7.23 (d, IH, J= 11.7 Hz), 7.15 (d, IH, J= 8.4 Hz), 6.70 (d, IH, J = 15.6 Hz), 5.02 (m, IH), 2.98 (s, 3H), 2.75 (t, 2H, J = 6.9 Hz), 1.50 (m, 2 H), 1.40 (d, 3H, J= 6.9 Hz), 1.32 (m, 2 H), 0.89 (t, 3H, J= 7.5 Hz).

Example 45: (K>3-(2-Butylamino-4-fluoro-phenyl)-N-[l-(3,5-difluoro-4- methanesulfonylamino-phenyl)-ethyl]- acrylamide

Step 1 : Synthesis ofN-memoxy-N-methyl-4-fluoro-2-n-buthylammo-benzamide

To a solution of N-methoxy-N-methyl-2-ammo-4-fluorobezoic acid amide

(0.35 g, 1.75 mmol), butyrylaldehyde (0.23 mL, 2.62 mmol), and AcOH (0.15 mL,

2.62 mmol) in dichloromethane (20 mL) was added sodium triacetoxyborohydride (0.74 g, 3.49 mmol) at 5 ⁰ C. The mixture was stirred for 5 hours at the same temperature and overnight at room temperature. The reaction was quenched by adding water. The organic layer was washed with saturated

aqueous NaHCO ₃ solution and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound quantitatively.

¹ H NMR(300MHz, CDCl ₃ ): δ 7.43 ~ 7.38 (m, 1 H), 6.35 ~ 6.24 (m, 2 H), 3.58 (s, 3 H), 3.33 (s, 3 H), 3.10 ~ 3.02 (m, 2 H), 1.67 ~ 1.35 (m, 4 H), 0.95 (t, 3 H, J - 7.2 Hz).

Step 2: Synthesis of 3-(4-fluoro-2-butylamino-phenyl)-acrylic acid methyl ester

To a solution of N-memoxy~N-methyl-4-fluoro-2-n-butylamino- benzamide (0.5 g, 1.97 mmol) in THF (8 mL) was added dropwise LiAlH ₄ (1 M in THF, 1.0 mL) at -45 ⁰ C. The mixture was stirred for 40 minutes at -35 ⁰ C and then quenched by adding saturated aqueous KHSO ₄ solution. The mixture was diluted with EtOAc, washed with 3 N HCl, and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was reacted with methyl (triρhenylphosphoranylidene)acetate (725 mg, 2.17 mmol) in toluene (4 mL) overnight at 100 ⁰ C. The mixture was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (0.15 g, 30%) after purification by column chromatography (EtOAc : hexane = 1 : 10).

¹ H NMRPOOMHZ ₅ CDCl ₃ ): δ 7.71 (d, 1 H, J= 15.9 Hz) ₅ 7.31 (t, 1 H, J= 8.4 Hz), 6.42 ~ 6.31 (m, 2 H), 6.26 (d, 1 H, J = 15.9 Hz), 4.13 (br ₅ 1 H) ₅ 3.15 ~ 3.09 (m, 2 H), 1.71 ~ 1.61 (m, 2 H), 1.49 ~ 1.41 (m, 2 H), 0.98 (t, 3 H, J= 7.2 Hz).

Step 3: Synthesis of ιffi)-N-fl-(3,5-Difluoro-4-methanesulfonylaminophenyl) ethyl]-3 -(4-fluoro-2-n-butylaminophenyl) acrylamide

To a solution of 3-(4-fluoro-2-butylamino-phenyl)-acrylic acid methyl ester (145 mg, 0.58 mmol) in THF (4 mL) and MeOH (2 mL) was added 1 N LiOH (4 mL). The mixture was stirred for 2 hours at room temperature, concentrated under reduced pressure, and then acidified with 3 N HCl. The mixture was diluted with EtOAc, washed with water, dried over anhydrous

magnesium sulfate, filtered, and concentrated under reduced pressure to give 3-(4- fluoro-2-butylamino-ρhenyi)-acrylic acid (120 mg, 88%) after purification by crystallization form EtOAc and hexane. To a mixture of 3-(4-fluoro~2- butylamino-phenyl)-acrylic acid (52 mg, 0.22 mmoϊ), (R)-[I -(3, 5-difluoro-4- methanesulfonylaminophenyl)ethylamine hydrochloride (64 mg, 0.22 mmol) and N-methylmorpholine (36 μL, 0.33 mmol) in THF (5 mL) was added 4-(4,6- dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholirium chloride hydrate (DMTMM, 68 mg, 0.25 mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was diluted with EtOAc and water, washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (4.5 mg, 4%) after trituration with ethyl ether. 2:1). 1H NMR(300MHz, CDCl ₃ ): δ 7.78 (d, 1 H, J= 14.7 Hz), 7.30 (t, 1 H, J= 6.9 Hz) ₅ 6.95 ~ 6.90 (m, 3 H) ₅ 6.36 ~ 6.30 (m, 2 H), 6.23 (d, 1 H, J= 14.7 Hz), 5.95 (d, 1 H, J= 6.6 Hz), 5.11 (t, 1 H, J= 6.9 Hz), 4.50 (bs, 1 H), 3.18 (s, 3 H), 3.10 (t, 2 H, J= 6.9 Hz), 1.68 ~ 1.58 (m, 2 H), 1.48 (d, 3 H, J- 6.9 Hz), 1.43 ~ 1.38 (m, 2 H), 0.95 (t, 3 H, J= 7.2 Hz). ESI [M-H] ^" : 468

Example 46: 3-(2-Butylamino-4-fluoro-phenyl)-N-(3,5-difluoro-4- methanesulfonylamino-benzyl)- acrylamide

To a mixture of 3-(4-fluoro-2-butylammo-phenyl)-acrylic acid (52 mg, 0.22 mmol), (3,5-difluoro~4-methanesulfonylamino)benzylamine hydrochloride

(61 mg, 0.22 mmol) and N-methylmorpholine (36 μL, 0.33 mmol) in THF (5 mL) was added 4-(4,6-dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholirium chloride hydrate (DMTMM, 68 mg, 0.25mmol). The mixture was stirred overnight at room temperature and then concentrated under reduced pressure. The residue was

. „ . _λ „ 2009/096701

diluted with EtOAc and water, washed with 2 N HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (45 mg, 45%) after trituration with ethyl ether. 1R NMR(300MHz, CDCl ₃ + DMSO-d6): δ 8.71 (bs, 1 H), 7.73 (br, 1 H), 7.68 (d, 1 H, J= 15.6 Hz), 7.30 (t, 1 H, J= 7.5 Hz), 6.97 (d, 2 H, J= 8.4 Hz), 6.40 ~ 6.30 (m, 3 H), 4.49 (d, 2 H, J- 6 Hz), 3.14 - 3.09 (m, 5 H), 1.69 ~ 1.59 (m, 2 H), 1.50 ~ 1.38 (m, 2 H), 0.96 (t, 3 H, J= 1.5 Hz).

Example 47: (λ)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyI ]- 3-(2-isobutyl-4-trifluoromethyI-phenyl)-acrylamide

3-(2-Isopropyl-4-trifluoromethyl-phenyl)-acrylic acid was obtained by the procedure in example 21. (R)-N-[4-(l-Ammo-ethyl)-2,6-difluoro-ρhenyl]-methanesulfona mide, HCl salt (55mg, 0.20mmol) was reacted with 3-(2-isobutyl-4-trifluoromethyl-phenyl)- acrylic acid (40mg, 0.15mmol) to give the title compound (18mg, 24%) after purification by recrystallization from ether.

¹ H NMR(300MHz, DMSO-d ⁶ ): δ 8.74 (d, IH, J= 7.8 Hz), 7.67 (m, 4H), 7.17 (d, 2H, J= 8.7 Hz), 6.70 (d, IH, J= 15.6 Hz), 5.03 (m, IH), 3.04 (s, 3H), 2.78 (t, 2H),

2.67 (m, IH), 1.47 (m, 2 H), 1.41 (d, 3H, J= 6.9 Hz), 1.31 (m, 2 H), 0.87 (m, 9H).

Example 48: (J¥)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyI)-ethy l]> 2-methyl-3-(2-propyI-4-trifluoromethyl-phenyI)-acrylamide

Step 1: Synthesis of 2-methyl-3-f2-propyl-4-trifluoromethyl-phenylVacrylic acid

To a suspension of N-methoxy-N-methyl-2-propyl~4-trifluoromethyl- benzamide (150mg, 0.58mmol) in THF (1OmL) was added dropwise 1.0M LiAlH ₄ (0.3OmL, 0.30mmol) at -78 ⁰ C. The mixture was warmed up to -2O ⁰ C and stirred for 30 mins. An aqueous solution of sodium potassium tartarate (10% w/v) was added to the reaction mixture and the resulting mixture was vigorously stirred for 30mins, to which was added Et ₂ O. After separation of two phases, the aqueous layer was extracted three times with ether and the combined organic layer was washed with brine, dried over anhyd. MgSO _4> filtered and concentrated under reduced pressure. The product was vacuum dried to yield the 2-propyl-4- trifluoromethyl-benzaldehyde. To an ice-cold suspension of NaH (60% in mineral oil, 45mg, 1.13mmol) in THF (2mL) was added triethyl-2-phosphonopropionate (O.lόmL, 0.75mmol), and the resulting mixture was stirred for lOmins at ambient temperature. A solution of aldehyde obtained above in THF was added to the reaction mixture and the resulting mixture was stirred for 3 hrs at ambient temperature. The reaction mixture was diluted with water and EtOAc ₅ and the aqueous layer was extracted three times with EtOAc. The combined organic layer was dried over anhydrous MgSO ₄ and concentrated under reduced pressure. The resulting residue was purified by column chromatography (gradient 12% to 100% EtOAc in Hex) to give 2-methyl-3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid ethyl ester (68mg ₅ 39%).

To a suspension of 2-methyl-3-(2-propyl-4-trifluoromethyl-phenyl)- acrylic acid ethyl ester (68mg, 0.23mmol) in THF (ImL) was added a solution of IN-LiOH (10 ml), and the mixture was stirred for 3 hours at room temperature. The resulting residue was dissolved in H ₂ O and then washed three times with EtOAc, acidified with IN HCl to pH 1-2. The solution was extracted three times

with methylene chloride and then dried over anhydrous MgSO ₄ and concentrated in vacuo to give the title compound (60mg, 96%).

¹ H NMR(300MHz ₅ CDCl ₃ ): δ 7.91(s, IH) ₅ 7.48(bs, 2H), 7.30(d, IH, J =8.7Hz), 2.63(t, 2H, J=8.1Hz), 1.96(s, 3H), 1.61(m, 2H), 0.95(t, 3H, J=7.2Hz).

Step 2: Synthesis of fi?)-N-[l-( ^' 3.,5~difluoro-4-methanesulfonylamino-phenvπ- ethyl]-2-methyl-3-(2-propyl-4-trifluoromethyl-ρhenyl)-acryl amide

To a suspension of (iζ)-N-[4-(l-amino-ethyl)~2,6-difluoro-phenyl]- methanesulfonamide, HCl salt (30mg, O.llmmol) in THF (2mL) was added N- methylmorpholine (23 1, 0.21mmol). The mixture was stirred for 5 minutes, to which were added 2-methyl-3-(2-propyl-4-trifluoromethyl-phenyl)-acrylic acid

(22mg, 0.081mmol) and 4-(4,6-dimethoxy[l,3,5]triazin-2-yl)-4- methylmorpholinium chloride hydrate (DMTMM ₅ 27mg, 0.098mmol). The mixture was stirred overnight at room temperature and was concentrated under reduced pressure. The residue was diluted with EtOAc and water. The organic layer was washed with saturated sodium bicarbonate, IN HCl and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by column chromatography (gradient 12% to 100% EtOAc in Hex) to give title compound (18mg, 44%).

¹ H NMR(SOOMHZ, DMSO-d6): δ 8.41 (d, IH ₅ J= 7.8 Hz), 7.58 (m, 2H) ₅ 7.41 (m, 2H), 7.13 (d, 2H, J = 8.4 Hz), 5.04 (m, IH), 2.97 (s, 3H) ₅ 2.62 (t, 2H), 1.86 (s, 3H), 1.52 (m, 2 H), 1.43 (d, 3H, J= 6.9 Hz) ₅ 0.87 (t, 3H ₅ J= 7.2 Hz).

Example 49: (/?)-N-[l-(3-Fluoro-4-methanesuIfonyIamino-phenyl)-etliyl]-2 - methyI~3-(2-propyl-4-trifluoromethyI-phenyl)-acrylamide

(R)-N-[4-(l-Amino-ethyl)-2-fluoro-phenyl]-methanesulfonam ide, HCl salt (52mg, 0.19mmol) was reacted with 2-methyl-3-(2-propyl-4-trifluoromethyl-

phenyl)-acrylic acid (40mg, 0.15mmol) to give the title compound (68mg, 93%) after purification by column chromatography (gradient 12% to 100% EtOAc in

Hex).

¹ H NMR(SOOMHZ ₅ DMSO-d6): δ 9.51 (bs, IH), 8.41 (d, IH ₅ J= 7.8 Hz) ₅ 7.58 (m,

2H), 7.29 (m, 5H) ₅ 5.06 (m, IH), 3.00 (s, 3H), 2.60 (t, 2H), 1.86 (s, 3H), 1.50 (m,

2 H), 1.44 (d, 3H ₉ J= 7.2 Hz), 0.87 (t, 3H, J= 7.5 Hz).

Example 50: (i?)-3-(2-CyclohexyImethoxy-4-trifluoromethyI-phenyl)-N-[l- (3,5~difluoro-4-methanesuIfonyIamino-phenyI)-ethyl]-acrylami de

1.LAH ₁ THF

Step3 2.Wittig,tolueπe

Step 1: Synthesis of 2-cvclohexylmethoxy-4-trifluoromethyl-benzoic acid cyclohexylmethyl ester

2-Hydroxy-4-trifluoromethyl-benzoic acid (246 mg, 1.19 mmol) was reacted with toluene-4- sulfonic acid cyclohexylmethyl ester (640 mg, 2.34 mmol) as described above to give the title compound (470 mg, 99 %) after purification by column chromatography. 1H NMR(300MHz, CDCl ₃ ): δ 7.83 (d, IH, J= 7.8 Hz), 7.20 (d, IH, 7= 7.8 Hz), 7.13 (s, IH), 4.13 (d, 2H, J-= 6.6 Hz), 3.84 (d, 2H, J= 5.7 Hz), 2.04 - 1.74 (m, 12H), 1.33 - 1.02 (m, 10H).

Step 2: Synthesis of 2-cvclohexylmethoxy-N-methoxy-N-methyl-4-trifluoro methyl-benzamide

2-Cyclohexylmethoxy-4-trifluoromethyl-benzoic acid cyclohexylmethyl ester (528 mg, 1.33 mmol) was reacted with IN LiOH (2.65 mg, 2.65 mmol) as described above to give 2-cyclohexylmethoxy-4-trifhioromethyl-benzoic acid (361 mg, 90 %) after drying by vacuum.

2-Cyclohexylmethoxy-4-trifluoromethyl-benzoic acid (361 mg, 1.19 mmol) was reacted with N,O-dimethylhydroxyamine, HCl salt (128 mg, 1.31 mmol) as described above to give the title compound (363 mg, 88 %) after purification by vacuum dry.

¹ H NMR(SOOMHZ, CDCl ₃ ): δ 7.36 (s, IH), 7.23 (d, IH, J= 7.5 Hz), 7.10 (s, IH), 3.83 (d, 2H, J = 5.7 Hz), 3.42 (s, 3H), 3.37 (s, 3H), 1.84 - 1.73 (m, 6H), 1.49 - 1.05 (m, 5H).

Step 3: Synthesis of 3-(2-cvclohexylmethoxy-4-trifluoromethyl-phenyl)-acrylic acid methyl ester

2-Cyclohexylmethoxy-N-methoxy-N-methyl-4-trifluoromethyl- benzamide (363 mg, 1.05 mmol) was processed by LAH reduction and wittig reaction as described above to give the title compound (250 mg, 69 %) after purification by column chromatography(n-Hex/EtOAc=20/l). 1H NMR(300MHz, CDCl ₃ ): δ 7.97 (d, IH, J= 16.2 Hz), 7.58 (d, IH, J= 7.8 Hz), 7.19 (d, IH, J= 7.8 Hz), 7.09 (s, IH), 6.60 (d, IH, J= 16.2 Hz), 3.86 (d, 2H, J = 5.7 Hz), 3.82 (s, 3H) ₅ 1.91 - 1.77 (m, 6H), 1.43 - 1.05 (m, 5H).

Step 4: Synthesis of 3-(2-cvclohexylmethoxy-4-trifluoromethyl-phenyl)-N-[ ^" l- (3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyll-acrylami de

N-[4-(l-Amino-ethyl)-2,6-difluoro-phenyl]-methanesulfonamide , HCl salt (28.8 mg, 0.101 mmol) was reacted with 3-(2-cyclohexylmethoxy-4- trifluoromethyl-phenyl)-acrylic acid (30 mg, 0.091 mmol) to give the title compound (33 mg, 65 %) after purification by column chromatography. 1H NMR(300MHz, CDCl ₃ ): δ 7.88 (d, IH, J= 15.6 Hz), 7.50 (d, IH, J= 8.1 Hz), 7.12 (d, IH, J- 8.1 Hz), 7.03 (s, IH) ₅ 6.94 (d, 2H, J= 8.4 Hz), 6.51 (d, IH, J = 15.9 Hz), 6.04 (s, IH), 5.82 (d, IH, J= 7.2 Hz), 5.17 - 5.10 (m, IH), 3.80 (d, IH, J- 5.7 Hz), 3.15 (s, 3H), 1.86 - 1.65 (m, 6H), 1.47 (d, 3H, J= 6.9 Hz), 1.28 - 1.02 (m, 5H).

Example 51: N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-piperidm -l-yI-4-trifluoromethyl-phenyl)~acrylaimde

N-(4-Aminomethyl-3,5-difluoro-phenyl)-methanesulfonamide, HCl salt

(59mg, 0.217mmol) was reacted with 3-(2-piperid-l-yl-4-trifluoromethyl- phenyl)-acrylic acid (65mg, 0.217mmol) to give the title compound (25mg, 22%) after purification by crystallization from Hex/EtOAc. 1H NMR(300MHz, CDCl ₃ ): δ 7.98(d, IH, J= 15.6Hz), 7.60(m, 2H), 6.99(m, 2H), 6.79(d, IH, J=8.4Hz), 6.46(d, IH, J=15.6Hz), 6.00(s, IH), 4.37(d, 2H, J=6.3Hz), 3 ,21(s, 3H), 2.92(m, 4H), 1.77(m, H), 1.61(m, 4H)

Example 52: (λ)-N-[l-(3,5-Difluoro-4-methanesuIfonyIamino-phenyl)-3-(2- piperidm~l-yl~4-trifluoromethyl-phenyϊ)~acrylamide

(R)-N-[4-(l-Amino-ethyl)-2,6-difluoro-phenyl]-methanesulfona mide, HCl salt (129mg, 0.451mmol) was reacted with 3-(2-piperid-l-yl-4-trifluoromethyl- phenyl)-acrylic acid (135mg, 0.451mmol) to give the title compound (65mg, 27%) after purification by crystallization from Hex/EtOAc. 1H NMR(300MHz, CDCl ₃ ): δ 7.94(d, IH ₅ J = 15.9Hz) ₅ 7.55(d ₅ IH ₅ J =8.4Hz), 7.23(m, 2H) ₅ 7.01(m, 2H) ₅ 6.43(d, IH ₅ J =15.6Hz), 5.99(s, IH) ₅ 5.83(s ₅ IH) ₅ 5.20(m, IH) ₅ 3.21(s ₅ 3H) ₅ 2.92(m ₅ 4H) ₅ 1.76(m, 4H) ₅ 1.59(m, 2H) ₅ 1.53(d, 3H ₅ J =6.6Hz).

Example 53: (2?)-N-[l-(3,5-Difluoro-4-methanesuIfonyIamino-phenyI)-ethyl ]- 3-(4-fluoro-2-propyI-phenyl)-acrylamide

3-(4-Fluoro-2-propyl-phenyl)-acrylic acid was prepared as described above. (R)-N-(4-Aminoethyl-2,6-difluoro-phenyl)-methanesulfonamide ₅ HCl salt (28 mg, 0.097 mmol) was reacted with 3-(4-fluoro-2-propyl-phenyl)-acrylic acid (15 mg ₅ 0.072 mmol), NMM (0.20 ml) and DMTMM (36 mg) at room temperature overnight to yield the title compound (12 mg, 38%) after column chromatography (Hex/EtOAc = 3/2). 1H NMR (300MHz ₅ CDCl ₃ ): δ 7.91 (d, IH ₅ J = 15.3 Hz), 7.00 (d, IH ₅ J = 8.4 Hz), 7.48 (m, IH) ₅ 6.92 (m, 2H), 6.25 (d, IH, J = 15.3 Hz) ₅ 6.05 (br ₅ IH) ₅ 5,82 (d, IH, J = 6.9 Hz), 5.17 (t, IH ₅ J- 7.1 Hz) ₅ 3.20 (s, IH) ₅ 2.72 (t, 2H, J = 7.5 Hz), 1.60 (m, 2H), 0.95 (t, 3H, J = 7.2 Hz)

Example 54: N-(3-Fluoro-4-methanesulfonylamino-5-vinyl-benzyl)-3-(2- isopropylamino-4-trifluoromethyl-phenyl)-acrylamide

N-(4-Aminomethyl-2,5-difluoro-phenyl)-methanesulfonamide, HCl salt (43mg, 0.154mmol) was reacted with 3-(2-isopropylamino-4-trifluoro-phenyl)- acrylic acid (42mg, 0.154mmol) to give the title compound (34mg, 42%) after purification by crystallization from Hex/EtOAc.

¹ H NMR(SOOMHZ, DMSO-d6): δ 8.71(s, IH), 7.70(d, IH, J =15.3Hz), 7.50(m, 2H), 7.10(m, 3H), 6.83(s, IH), 6.57(d, lH _s J=15.3Hz), 5.85(m, IH), 5.70(m, IH), 5.42(m, IH) ₅ 4.42(d, 2H, J =5.4Hz) ₅ 3.58(m, IH), 2.98(s, 3H) ₅ 1.18(d, 6H ₅ J =6.0Hz). ESI [M-H] ^" : 498

Example 55: (2?J-N-[l-(3,5-Difluoro-4-methanesulfonyIamino-phenyl)-ethyl ]- 3-(2-propylamino-4-trifluoromethyl-phenyl)-propionamide

(R)-N-[l-(3,5-Difluoro-4-methanesulfonylamino-phenyl)-ethyl] -3-(2- propylamino-4-trifluoromethyl-phenyl)-acrylamide (12 mg) was reduced with Pd/C (15 mg) under hydrogen atmosphere to yield title compound (7 mg, 60%). ¹ H NMR (300MHz ₅ CDCl ₃ ): δ 7.02 (d, IH ₅ J = 7.5 Hz), 6.95 (d, IH ₅ J = 8.7 Hz) ₅ 6.87-6.71 (m, 3H) ₅ 6.17 (br, IH), 5.62 (d, IH, J = 7.8 Hz), 4.96 (t, IH ₅ J = 7.2 Hz), 3.15 (s, 3H), 3.00 (m, 2H), 2.83 (m, 2H), 2.47 (m, 2H), 1.32 (d, 3H ₅ J = 6.6 Hz), 0.96 (t, 3H, J = 7.5 Hz).

Example 56: N-(3,5-Difluoro-4-methanesuIfonyIamino-benzyl)-3-(2- propylamino-4-trifluoromethyl-phenyl)-propionamide

N-(3,5-Difluoro-4-methanesulfonylamino-benzyl)-3-(2-propylam ino-4- trifluoromethyl-phenyl)-acrylamide (20 mg, 0.041 mmol) was reduced with Pd/C under hydrogen atmosphere to yield title compound (12 mg ₅ 59%). 1H NMR (300MHz, CDCl ₃ ): δ 7.08 (d, IH, J = 7.5 Hz) ₅ 6.95 (d, IH, J = 8.4 Hz), 36.87 (d, IH, J = 7.8 Hz), 6.78 (s, IH), 6.76 (m, IH), 6.29 (s, IH), 5.93 (t, IH), 4.36 (d, 2H, J = 6.3 Hz), 3.19 (s, 3H), 3.09 (m, 2H), 2.91 (m, 2H), 2.55 (m, 2H), 1.70 (m, 2H), 1.02 (t, 3H, J = 7.5 Hz)

Experimental example: Biological potency test

1. ⁴⁵ Ca influx test

1) Separation of spinal dorsal root ganglia (DRG) in newborn rats and primary culture thereof

Neonatal (2-3 day old or younger than 2-3 day old) SD rats were put in ice for 5 minutes to anesthetize and disinfected with 70% ethanol. DRG of all part of spinal cord were dissected (Wood et al, 1988, J. Neurosci. 8, ρρ3208-3220) and collected in DME/F12 medium to which 1.2g/l sodium bicarbonate and 50mg/l gentamycin were added. The DRG were incubated sequentially at 37 ⁰ C for 30 mins in 200 U/ml collagenase and 2.5mg/ml trypsin, separately. The ganglia were washed twice with DME/F12 medium supplemented with 10% horse serum, triturated through a fire-polished Pasteur pipette, filtered through Nitex 80 membrane to obtain single cell suspension and the suspension was washed once more. This was subjected to centrifugation, then resuspended in cell

culture medium at certain level of cell density. As the cell culture medium, DME/F12 medium supplemented with 10% horse serum was diluted with identical medium conditioned by C6 glioma cells 2 days on a confluent monolayer (1 :1), and NGF (Nerve Growth Factor) was added to adjust 200ng/ml as final concentration. After the cells were grown 2 days in medium where cytosine arabinoside (Ara-C, 100 μM) was added to kill dividing nonneuronal cells, medium was changed to one without Ara-C. The resuspended cells were plated at a density of 1500-2000 neurons/well onto Terasaki plates previously coated with 10 μg/ml poly-D-ornithine.

2) ⁴⁵ Ca influx experiments

DRG nerve cells from the primary culture of 2 days were equilibrated by washing 4 times with HEPES (1OmM, pH 7.4)-buffered Ca ²⁺ , Mg ²⁺ -free HBSS (H-HBSS). The solution in each well was removed from the individual well. Medium containing the test compound plus capsaicin (final concentration 0.5 μM) and ⁴⁵ Ca (final concentration 10 μCi/ml) in H-HBSS was added to each well and incubated at room temperature for 10 mins. Terasaki plates were washed five times with H-HBSS and dried at room temperature. To each well, 0.3% SDS (10 μl) was added to elute ⁴⁵ Ca. After the addition of scintillation cocktail of into each well, the amount of ⁴⁵ Ca influx into neuron was measured by counting radioactivity. Antagonistic activities of test compounds against vanilloid receptor were calculated as percent of the inhibition of maximal response of capsaicin at a concentration of 0.5 μM. The results are displayed in Table 1 below.

[Table 1 J Results of Calcium Influx Test

2. Analgesic activity test: Mouse writhing test by inducing with phenyl-p- quinone

Male ICR mice (mean body weight 25g) were maintained in a controlled lighting environment (12 h on/ 12 h off) for experiment. Animals received an intraperitoneal injection of 0.3ml of the chemical irritant phenyl-p-quinone (dissolved in saline containing 5% ethanol to be a dose of 4.5mg/kg) and 6 mins later, the number of abdominal constrictions was counted in the subsequent 6 mins period. Animals (10 animals/group) received 0.2ml of test compounds solution in vehicle of ethanol/Tween 80/saline (10/10/80) intraperitoneally 30 min before the injection of phenyl-p-quinone. In the case of oral administration, 0.2ml of test compounds solution in vehicle of ethanol/Tween 80/saline (5/5/90) were administered 54 min prior to the 0.2ml of 0.02% phenyl-p-quinone injection. A reduction in the number of writhes responding to the test drug compound relative to the number responding in saline control group was considered to be indicative of an analgesic effect. Analgesic effect was calculated by % inhibition equation (% inhibition^C-TyC x 100), wherein C and T represent the number of writhes in control and compound-treated group, respectively. Most examples of the present disclosure having good in vitro activities, were tested at various doses (ranging from 0.3 to 3 mg/kg) and all compounds tested in vivo showed analgesic effects from 8 to 59% inhibition at each dose, respectively.

3. PK study

Pharmacokinetics of compounds in rats were analyzed using the following experiment. Rats were fasted overnight prior to administration and until approximately 4 hrs after administration. Rats were given a single oral administration of compound at same dose. Administration volume was 10ml/kg.

Blood samples were collected from the retro-orbital sinus at various times over the following 7 hrs. Immediately after each collection, plasmas were separated from blood cells by centrifugation and stored at -20 ^° C until the analysis was performed. The plasma samples were analyzed using a reverse phase high- performance chromatography (HPLC) method. The results are displayed in table 2 below.

[ Table 2 ] PK results for the compound having CF3 -phenyl with meta substituent

4. Comparative examples

As shown in Tables 2 and 3, the PK properties of the compounds of formula (I) of the present disclosure surprisingly have superior PK characteristics compared to compounds with a tert-butyl phenyl partial structure, with or without other substituents on the phenyl group, which were at least in part disclosed in the art, e.g. in WO 06/101318 or WO 06/101321 (also refer Table 3). Substantial increases in absorption and apparent half-life were observed by the replacement of tert-butyl phenyl by F-phenyl or CF ₃ - phenyl (see Table 2 vs 3).

[Table 3] PK results for the compound having tert-butyl-phenyl

a Example number in WO 06/101318 b could not be determined due to low plasma concentration (detection limit : 0.100mcg/ml). c Example number in WO 06/101321

As shown in Tables 2 and 4, the compounds of formula (I) of the present disclosure have superior IC ₅₀ values and in some cases also improved PK characteristics compared to compounds with a CF ₃ -phenyl partial structure but without additional substituents on the phenyl group, which were at least in part disclosed in the art, e.g. in WO 06/101318 or WO 06/101321. Surprisingly, the introduction of an additional substituent in ortho position of the phenyl's attachment position to the cinnamoyl backbone confers improved VRl activity to the compounds. For example, whilst comparative compound "G" has an IC50 value of more than 10 μM, the compounds 1, 3,5-7,10,16-18, 21, 24, 26, 31, 39, 47, 50, and 52 of the present disclosure which all differ from "G" only by additional substituent(s) on phenyl group, all have IC50 values in a range between 0.019 and 0.34 μM. In addition, compound "G" shows only poor PK-properties, while all tested compounds of the present disclosure showed improved PK properties (in terms of T max and AUC). Likewise, while comparative compound "F" has a moderate IC ₅₀ value of 0.57 μM, the IC ₅₀ values of the corresponding examples of the present disclosure Ex 12 (0.15 μM) and 54 (0.027 μM) are significantly improved.

[Table 4] PK results for the compound having CF3-phenyl

a Example number in WO 06/101318 b could not be determined due to low plasma concentration (detection limit : O.lOOmcg/ml).

In summary, the presently disclosed compounds of formula (I) show a significantly improved "balance" between VRl activity and PK properties compared to the compounds disclosed in the art.

INDUSTRIAL APPLICABILITY

As explained above, the compound according to the present disclosure is useful to prevent or to treat pain, inflammatory disease of the joints, neuropathies, HlV-related neuropathy, nerve injury, neurodegeneration, stroke, urinary bladder hypersensitivity including urinary incontinence, cystitis, stomach duodenal ulcer, irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD), fecal urgency, gastro-esophageal reflux disease (GERD), Crohn's disease, asthma, chronic obstructive pulmonary disease, cough, neurotic/allergic/inflammatory skin disease, psoriasis, pruritus, prurigo, irritation of skin, eye or mucous membrane, hyperacusis, tinnitus, vestibular hypersensitivity, episodic vertigo, cardiac diseases such as myocardial ischemia, hair growth-related disorders such as effluvium, alopecia, rhinitis, and pancreatitis.

More specifically, the compound according to the present disclosure is

useful to preventing and treating of pain, which is or which is associated with a condition selected from the group consisting of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, diabetic neuropathic pain, post-operative pain, dental pain, non-inflammatory musculoskeletal pain (including fibromyalgia, myofascial pain syndrom and back pain), migraine, and other types of headaches.

While the invention has been described with respect to the above specific embodiments, it should be recognized that various modifications and changes may be made to the invention by those skilled in the art which also fall within the scope of the invention as defined by the appended claims.