AU2002239884A1 - Imidazolyl derivatives as corticotropin releasing factor inhibitors - Google Patents

Description

IMIDAZOLYL DERIVATIVES AS CORTICOTROPIN RELEASING

FACTOR INHIBITORS

Field of the Invention The present invention relates to antagonists and pharmaceutical compositions comprising said antagonists of the corticotropin releasing factor receptor ("CRF receptor") useful for the treatment of depression, anxiety, affective disorders, feeding disorders, post-traumatic stress disorder, headache, drug addiction, inflammatory disorders, drug or alcohol withdrawal symptoms and other conditions the treatment of which can be effected by the antagonism of the CRF-1 receptor.

Background of the Invention It has been shown that the neuropeptide, corticotropin releasing factor ("CRF"), acting through its binding to the CRF-1 receptor, is a primary mediator of stress- and anxiety-related physiological responses in humans and other mammals by stimulating ACTH secretion from the anterior pituitary gland. See AJ. Dunn, et al., Brain Res. Rev., 15: 71-100 (1990). Antagonists of the CRF-1 receptor, both peptides (J. Gulyas, et al., Proc. Natl. Acad. Sci. U.S.A., 92: 10575-10579 (1995) and small molecules (J.R. McCarthy, et al., Curr. Pharm. Design, 5: 289-315 (1999), have demonstrated the ability to ameliorate the effects of stressful stimuli in several animal models. In addition, marked elevations of CRF in cerebrospinal fluid have been detected in a large portion of individuals diagnosed with major depression and anxiety disorders, and the levels correlate with severity of the disease. See F. Holsboer, J. Psychiatric Res., 33: 181-214 (1999). Following antidepressant treatment, the increased CRF levels observed in depressed patients were reduced. See CM. Banki, et al., Eur. Neuropsychopharmacol., 2: 107-113 (1992); see also Effects of the high-affinity corticotropin-releasing hormone receptor 1 antagonist R121919 in major depression: the first 20 patients treated. Zobel AW, Nickel T, Kunzel HE, Ackl N, Sonntag A. Ising M, Holsboer F J Psychiatr Res 2000, 34, 171- 181. CRF has also been shown to be a key mediator of several immune system functions through its effect on glucocorticoid plasma levels. See E.L. Webster, et al., Ann. N.Y. Acad. Sci., 840: 21-32 (1998). Recent reviews of the activity of CRF-1 antagonists include P J. Gilligan, et al., J. Med. Chem., 43: 1641-1660 (2000) and J.R. McCarthy, et al., Ann. Rep. Med. Chem., 34: 11-20 (1999). There appears a need to discover novel small molecule CRF antagonists in order to treat a wide variety of human disorders including depression, anxiety, bipolar disorder, and other stress-related illnesses. See WO 98/35967, WO 99/01454, WO 99/10350, wo 99/67247, 00/01675, WO 00/01697, WO 00/39127, WO 00/59907, WO 00/59908, EP 778277, EP 812831.

Summary of the Invention Thus according to a first embodiment of the first aspect of the present invention are provided compounds of Formula (I)

and pharmaceutically acceptable salts and solvates thereof wherein

R¹ is H, C_halky!, -βhaloalkyl, cyano, halo, C₃. ₇cycloalkyl, -Cι_₆alkylene-C₃. cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl;

R²is C(D)NR³R⁴, D'- D"(R³)(R⁴) or CH₂N R³R⁴ D' is CH₂ or a bond; D" is C, C-OH or CH wherein said C is attached to R³ by a single or double bond; said C is attached to R⁴by a single or double bond; provided that C is not attached to both R³ and R⁴ by double bonds; said CH is attached to R³ and R⁴ by single bonds; said C of C-OH is attached to R³ and R⁴ by single bonds; D is O or S;

R³ and R⁴ are each independently selected from the group consisting of H, Cι_₆alkyl, C].₆haloalkyl, -Cι_₆hydroxyalkyl, -Ci.

₄alkylene-O-Cι.₄alkyl, -Ci-salkylene-Ci.ethioalkyl, -C₂. ₆alkylidene-(Cι_₄alkoxy)₂, C₃_ cycloalkyl, -Cι_₆alkylene- C₃.₇cycloalkyl, C₂.₆alkenyl, C₃.₆alkynyl, -C^alkylene-CN, -C ₆alkylene-heterocyclo and -Cι.₆alkylene-aryl; wherein said aryl of said -Cι_₆alkylene-aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro, Cι- alkyl and Cι_₃. alkoxy; or

R³ and R⁴ together with the nitrogen to which they are attached form a five or six-membered heterocycle, said heterocycle optionally containing one additional heteroatom selected from the group consisting of N, S and O; and said heterocycle optionally substituted with one or more groups selected from the group consisting of Cι_₆alkyl, Cι_₆alkoxy, aryl, -Cι_₄alkylene- aryl, pyridyl and halogen; wherein said aryl of said -Ci.₄alkylene- aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro and C^alkoxy; X is C; Y is C;

A is

wherein

X¹ is N and is attached to X; Y¹ is N and is attached to Y;

G is

wherein

Y² is N, CH, CH₂, C(O), C(S), CR⁵, CHR⁵ or CE¹ and is attached to Y¹;

J is CH, CH₂ , C(O), C(S), CR⁶, CHR⁶, a bond or CE²;

Z¹ is CH, CH₂, C(O), C(S), CR⁷, CHR⁷ or CE³ and is attached to Z; wherein R⁵, R⁶ and R⁷ are each independently selected from the group consisting of -CN, -Cι- . alk(en)ylene-CN, halo, Cι_₆alkyl, C₂. ₆alkenyl, C₃.₆alkynyl, Cι_₆haloalkyl, aryl, -C_!.₄alk(en)ylene-aryl, -Cι_₄- alk(en)ylene-heterocyclo, heterocyclo, - Cι.₄alk(en)ylene- amino, -C].₄alkylene- amino-Cι_ alkyl, aryl-amino, -amino-(C- ₁.₆alk(en)yl)₁.₂, -amino-aryl, -amino- 5 heterocyclo, Cι_₆alkoxy, -O-aryl and -

O-heterocyclo;

E¹ and E² together form moieties selected from the group consisting of C -alk(en)lyene, N(CH)₃, CHN(CH)₂, N(CH)₂N, 10 N=NCH=N and NCHNCH; wherein said moieties are optionally substituted with halogen, -CN, Cι-C alkyl, C₃-C₆cycloalkyl, substituted or unsubstituted 15 phenyl, hydroxy, C]-C alkoxy,

SH, Cι-C₄thioalkyl, NH₂, NH(Cι-C₄alkyl) orN(Cι- C₄alkyl)₂;

E and E together form moieties selected from 20 the group consisting of C -alk(en)lyene,

N(CH)₃, CHN(CH)₂,N(CH)₂N, N=NCH=N and NCHNCH; wherein said moieties are optionally substituted with halogen, -CN,

25 Ci-C₄alkyl, C₃-C₆cycloalkyl, substituted or unsubstituted phenyl, hydroxy, Cι-C alkoxy, SH, d-C₄thioalkyl, NH₂,

30 C₄alkyl)₂; E¹ and E³ together form moieties selected from the group consisting of C -alk(en)lyene, N(CH)₃, CHN(CH)₂, N(CH)₂N, N=NCH=N and NCHNCH; wherem said moieties are optionally substituted with halogen, -CN, Cι-C₄alkyl, C₃-C₆cycloalkyl, substituted or unsubstituted phenyl, hydroxy, Cι-C₄alkoxy, SH, d-C₄thioalkyl, NH₂,

NH - alkyD orN d- C₄alkyl)₂;

Z is N-V, wherein N is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of C^alkyl, Cι_ alkoxy, Cι_₆thioalkyl, Cι-₄haloalkyl, halogen, Ν(Cι-C alkyl)₂ and CN; and provided that if Y² is N, then J is a bond and Z¹ is not CE³; if Y² is CE¹ and Z¹ is CE³, then I is a bond ; if Y² is not CE¹ and Z¹ is not CE³, then J is not CE²; if J is CE², then

Y² is CE¹ and Z¹ is not CE³, CR⁷ or CHR⁷; or

Z¹ is CE² and Y² is not CE¹, CR⁵ or CHR⁵.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is phenyl or 3-pyridyl and is substituted with two to three of the same or different substitutents selected from the group consisting of Cι- alkyl, Ci- ₄alkoxy, Cι_₆thioalkyl, Cι.₄haloalkyl, halogen, N(Cι-C₄alkyl)₂ and CN; said substituents attached at the 2, 4 or 6-positions of said phenyl or said 3-pyridyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is 2-pyridyl and is substituted with two of the same or different substitutents selected from the group consisting of Cι_ alkyl, Q.₄alkoxy, . ₆thioalkyl, Cι_₄haloalkyl, halogen, N(Cι-C alkyl)₂ and CN; said substituents attached at the 3 and 5-positions of said 2-pyridyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R¹ is Cι_₆alkyl or ^haloalkyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R¹ is methyl or trifluoro methyl. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R²is C(D)NR³R⁴.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is C(D)NR³R⁴ and D is O.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R²is C(D)NR³R⁴ and D is S.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is CH₂N R³R⁴.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is D'- D" (R³)(R⁴), D is a bond and D" is C-OH. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R²is D'- D"(R³)(R⁴), D is a bond and D" is C or CH. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is D'- D" (R³)(R⁴), D is a CH₂ and D" is C-OH.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is D' - D" (R³)(R⁴), D is CH₂ and D" is C or CH.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R³ and R⁴ are each independently selected from the group consisting of H, Cι_₆alkyl, Cι_₆haloalkyl, -Ci..₆hydroxyalkyl, -Cι_

₃alkylene-Cι_₆thioalkyl, -C₂_₆alkylidene-(C₁.₄alkoxy)₂, C₃. cycloalkyl, -Cι_₆alkylene- C₃_ cycloalkyl, C₂.₆alkenyl, C₃_₆alkynyl, -C^alkylene-CN, -Cι_₆alkylene-heterocyclo and -Cι.₆alkylene-aryl; wherein said aryl of said - -_όalkylene-aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro, ^alkyl and Cj.₃alkoxy.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R³ and R⁴ are each independently selected from the group consisting of H, Cj[-₆alkyl, d-₆haloalkyl, -Ci-_όhydroxyalkyl, -C^alkylene-O-C^alkyl, -Cι_ ₃alkylene-Cι_₆thioalkyl, -C₂.₆alkylidene-(C₁.₄alkoxy)₂, C . cycloalkyl, -Cι_₆alkylene- C₃.₇cycloalkyl, C₂.₆alkenyl, C₃.₆alkynyl and -Ci-βalkylene-CN.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R³ and R⁴ together with the nitrogen to which they are attached form a five or six-membered heterocycle, said heterocycle optionally containing one additional heteroatom selected from the group consisting of N, S and O; and said heterocycle optionally substituted with one or more groups selected from the group consisting of Cι_₆alkyl, Ci-₆alkoxy, aryl, -Cι_ alkylene-aryl, pyridyl and halogen; wherein said aryl of said -Cι_ alkylene-aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro and C^alkoxy.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R³ and R⁴ together with the nitrogen to which they are attached form a five or six-membered heterocycle, said heterocycle optionally containing one additional heteroatom selected from the group consisting of N, S and O.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R³ and R⁴ together with the nitrogen to which they are attached form a five or six-membered heterocycle.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein J is a bond .

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹ and Z¹ is CE³ . According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹ and Z¹ is CE³.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein J is CE².

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is substituted 3-pyridyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is substituted phenyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is 2, 4, 6-trimethylphenyl. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein V is 2,4-dichlorophenyl. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R⁵, R⁶ and R⁷ are each independently selected from the group consisting of halogen, Q-βalkyl, Cι_₆haloalkyl, benzyl, phenyl, Cι_₃alkyl-imidazolyl, Ci.₃alkyl-indolyl and Cι.₃alkyl-pyridyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH₂, J is a bond and Z¹ is CH₂.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH, J is a bond and Z¹ is CH.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CR⁵, 1 is a bond and Z¹ is CH wherein said R⁵ is halo. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH, I is a bond and Z¹ is CR⁷ wherein said R⁷ is halo.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH, J is a bond and Z¹ is CR⁷ wherein said R⁷ is halo, cyano or Ci-βalkyl.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is C(O), J is a bond and Z¹ is CH . According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH₂ , J is a bond and Z¹ is C(O).

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CH₂, J is a bond , Z¹ is CH₂, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is ethyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CH₂, J is a bond , Z¹ is CH₂, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R² is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CH₂, J is a bond , Z¹ is CH₂, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is ethyl, R²is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CH₂, J is a bond , Z¹ is CH₂, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein Y² is CH , J is CH₂ and Z¹ is CH₂.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is CN or CF₃ and Y² is CH₂, J is CH₂ and Z¹ is CH₂.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is C(O), J is CH and Z¹ is CH.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CH , J is CH and Z¹ is C(O).

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is C(O), J is CE² and Z¹ is CE³ wherein E² and E³ together form C -alk(en)lyene optionally substituted with halogen.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹, J is CE² and Z¹ is C(O) wherein E¹ and E² together form C₄-alk(en)lyene optionally substituted with halogen. According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is C(O), J is CE² and Z¹ is CE³ wherein E² and E³ together form N(CH)₃, CHN(CH)₂,N(CH)₂N, N=NCH=N or NCHNCH optionally substituted with halogen.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹, J is CE² and Z¹ is C(O) wherein E¹ and E² together form N(CH)₃, CHN(CH)₂, N(CH)₂N, N=NCH=N or NCHNCH optionally substituted with halogen.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form C₄-alk(en)lyene optionally substituted with halogen.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃ optionally substituted with halogen, methoxy, methyl or nitrile.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein R² is CH₂NR³R⁴, R³ is ethyl or propyl, R⁴ is -(CH₂)₂-phenyl, Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃ optionally substituted with halogen, methoxy, methyl or nitrile.

According to another embodiment of the first aspect of the present invention are provided compounds of Formula (I) according to the first embodiment of the first aspect wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃, CHN(CH)₂,N(CH)₂N, N=NCH=N or NCHNCH optionally substituted with halogen.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=C(F)CH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl. According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl. According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is ethyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cycloρroρyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl. According to another embodiment of the first aspect of the present invention

1 9 is provided a compound of Formula (I) wherein R is trifluoromethyl, R is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl- phenyl. According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R²is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4-dichloro-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherem R¹ is ethyl, R² is C(O)NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=C(F)CH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R² is CH NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=C(F)CH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is methyl, R² is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is ethyl, R²is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl. According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R is trifluoromethyl, R is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=CHCH=CH-, Z is N-V and V is 2,4,6-trimethyl- phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein R¹ is ethyl, R² is CH₂NR³R⁴, R³ is propyl, R⁴ is -CH₂-cyclopropyl, Y² is CE¹, J is a bond , Z¹ is CE³, E¹ and E³ together form -CH=C(F)CH=CH-, Z is N-V and V is 2,4,6-trimethyl-phenyl.

According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein "aryl" or "ar-" is phenyl or napthalenyl. According to another embodiment of the first aspect of the present invention is provided a compound of Formula (I) wherein "heterocyclic" or "heterocyclo" is furyl, thienyl, benzothienyl, thiazolyl, imidazolyl, oxazolyl, oxadiazolyl, thiadiazolyl, benzthiazolyl, triazolyl, tetrazolyl, isoxazolyl, isothiazolyl, pyrrolyl, pyranyl, tetrahydropyranyl, pyrazolyl, pyridyl, pyrimidinyl, quinolinyl, isoquinolinyl, purinyl, carbazolyl, benzoxazolyl, benzimidazolyl, indolyl, isoindolyl, pyrazinyl, azetidinyl, piperidyl, piperazinyl, imidazolinyl, thiazolidinyl, 3-pyrrolidin-l-yl, morpholinyl, thiomorpholinyl or tetrahydropyranyl.

According to another embodiment of the first aspect of the present invention are compounds of Formula (I) and salts or solvates thereof selected from the group consisting of 2-methyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazo[l,2- α]imidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, 2-ethyl-7-(2,4,6- trimethylphenyl)-6,7-dihydro-5H-imidazo[l,2-α]imidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, 5-fluoro-2-methyl-8-(2,4,6-trimethylphenyl)-8H- l,3a,8-triaza-cyclopenta[ ]indene-3-carboxylic acid cyclopropylmethyl-propyl- amide, 2-methyl-8-(2,4,6-trimethylphenyl)-8H-l,3a,8-triaza-cyclopenta[a]indene-3- carboxylic acid cyclopropylmethyl-propyl-amide, 2-ethyl-8-(2,4,6-trimethylphenyl)- 8H-l,3a,8-triaza-cyclopenta[α]indene-3-carboxylic acid cyclopropylmethyl-propyl- amide, 2-trifluoromethyl-8-(2,4,6-trimethylphenyl)-8H-l ,3a,8-triaza- cyclopenta[α]indene-3-carboxylic acid cyclopropylmethyl-propyl-amide, 8-(2,4- dichlorophenyl)-2-methyl-8H-l,3a,8-triaza-cyclopenta[α]indene-3-carboxylic acid cyclopropylmethyl-propyl-amide, 2-ethyl-5-fluoro-8-(2,4,6-trimethylphenyl)-8H- 1 ,3a,8-triaza-cyclopenta[ ]indene-3-carboxylic acid cyclopropylmethyl-propyl- amide, cyclopropylmethyl-[5-fluoro-2-methyl-8-(2,4,6-trimethylphenyl)-8H-l,3a,8- triaza-cyclopenta[α]inden~3-ylmethyl]-ρropyl-amine, cyclopropylmethyl-[2-methyl- 8-(2,4,6-trimethylphenyl)-8H-l,3a,8-triaza-cyclopenta[α]inden-3-ylmethyl]-propyl- amine, cyclopropylmethyl-[2-ethyl-8-(2,4,6-trimethylphenyl)-8H-l,3a,8-triaza- cyclopenta[β]inden-3-ylmethyl]-propyl-amine, cyclopropylmethyl-propyl-(2- trifluoromethyl-8-(2,4,6-trimethylphenyl)-8H-l,3a,8-triaza-cyclopenta[ ]inden-3- ylmethyl)-amine and cyclopropylmethyl-[2-ethyl-5-fluoro-8-(2,4,6-trimethyl- phenyl)-8H-l,3a,8-triaza-cyclopenta[α]inden-3-ylmethyl]-propyl-amine. According to another embodiment of the first aspect of the present invention are compounds of Formula (I) and salts or solvates thereof selected from the group consisting of Cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-[2-trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazo[l,2-a]pyrimidin-3-ylmethyl]-amine,

Cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-[2-trifluoromethyl-8-(2,4,6- trimethylphenyl-8H-l,3a,8-triaza-cyclopenta[α]inden-3-ylmethyl]-amine,

Ethyl-[2-methyl-8-(2,4,6-trimethyl-ρhenyl)-8H-l,3a,7,8-tetraaza- cyclopenta[α]inden-3-ylmethyl]-phenethyl-amine,

Cyclobutylmethyl-[2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cycloρenta[α]inden-3-ylmethyl]-propyl-amine, [8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8Η-l,3a,7,8-tetraaza- cyclopenta[a]inden-3-ylmethyl]-phenethyl-propyl-amine,

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[α]inden-3-ylmethyl]-cyclobutylmethyl-propyl-amine,

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8Η-l,3a,7,8-tetraaza- cyclopenta[a]inden-3-ylmethyl]-ethyl-phenethyl-amine,

8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-3-(3-phenyl-pyrrolidin-l- ylmethyl)-8H-l,3a,7,8-tetraaza-cyclopenta[α]indene,

6-Chloro-2-ethyl-7-(2,4-dichlorophenyl)-7Η-imidazo[l,2-a]imidazole-3- carboxylic acid N,N-dipropylamide, 3-[(N,N-Dipropylamino)methyl]-6-chloro-2-ethyl-7-(2,4-diclorophenyl)-7H- imidazo[l ,2-a]imidazole, 6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazo[l,2-a]imidazole-3- carboxylic acid N-cyclopropylmethyl-N-ethylamide,

3-[(N-Cyclopropylmethyl-N-ethylamino)methyl]-6-chloro-2-ethyl-7-(2,4,6- trimethylphenyl)-7H-imidazo [ 1 ,2-a]imidazole, 6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-amine,

6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)-amine,

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclopropylmethyl-ethyl-amine,

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclobutylmethyl-(2,2,2-trifluoro-ethyl)-amine,

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-propyl-(3,3,3-trifluoro-propyl)-amine, [6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-ethyl-phenethyl-amine,

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-(2-cyclopropyl-ethyl)-(3,3,3-trifluoro-propyl)-amine, and

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-(2-cyclopropyl-ethyl)-(2,2,2-trifluoro-ethyl)-amine.

According to various embodiments of a second aspect of the present invention are provided pharmaceutical compositions comprising compounds of Formula (I) as defined herein.

According to various embodiments of a second aspect of the present invention are provided methods of treating depression, anxiety, affective disorders, post- traumatic stress disorder, post-operative stress, headache, drug addiction, eating disorders and obesity, sudden death due to cardiac disorders, iritable bowel syndrome, hypertension, syndrome X, inflammatory disorders, stress-induced immune suppression, infertility, stress-induced insomnia and other sleep disorders, seizures, epilepsy, stroke and cerebral ischemia, traumatic brain injury, yet other disorders requiring neuroprotection, drug or alcohol withdrawal symptoms, other disorders including tachycardia, congestive heart failure, osteoporosis, premature birth, psychosocial dwarfism, ulcers, diarrhea, post-operative ileus and yet other conditions the treatment of which can be effected by the antagonism of the CRF-1 receptor by the administration of pharmaceutical compositions comprising compounds of the present invention as described herein.

According to a first embodiment of a third aspect of the present invention are provided compounds of Formula (WHET)

wherein

R¹ is H, Cι.₆alkyl, Cι„₆haloalkyl, Cι_₆alkoxy, Cι-₆thioalkyl, cyano, halo, C₃.₇cycloalkyl, -Cι_₆alkylene-C₃.₇cycloalkyl, C₂-₆alkenyl or C₃-₆alkynyl;

R⁸ is O-Cι-₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

Xis C;

Y is C;

X¹ is N;

Y¹ is N;

Y² is CH₂;

J is CH₂ or a bond;

Z^l is H₂ r C(P); aaά

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_ alkyl, d.₄alkoxy, Cι.₆thioalkyl, Cι_ haloalkyl, halogen, N(d-C₄alkyl)₂ and CN. According to another embodiment of a third aspect of the present invention are provided processes for preparing compounds of Formula (WHH)

wherein

R¹ is H, Cι.₆alkyl, Cι-₆haloalkyl, Cι_₆alkoxy, d.βthioalkyl, cyano, halo, C₃_₇cycloalkyl, -Cι.₆alkylene-C .₇cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl; R⁸ is O-d_₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C;

X¹ is N;

Y¹ is N; Y² is CH₂;

J is CH₂ or a bond; z s CHa or Q ^ and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_ alkyl, Cι_ alkoxy, C^thioalkyl, d_

₄haloalkyl, halogen, N(Cι-C₄alkyl)₂ and CN;

comprising reacting a compound of Formula (UFF)

wherein

Z, Z¹, J and Y² are defined as for Formula (WHH);

with a compound of Formula (UFF ')

wherein

R¹, R⁸ , X, Y, X¹ and Y¹ are defined as for Formula (WHH); in the presence of a suitable base and polar aprotic solvent to yield a compound of Formula (VGG)

wherein

R¹, R⁸ , X, Y, X¹, Y¹, Y², J, Z¹ and Z are defined as for Formula

(WHH);

and reacting said compound of Formula (VGG) with a high-boiling point polar aprotic solvent and a suitable silver salt under suitably high temperature.

According to another embodiment of a third aspect of the present invention are provided compounds of Formula ( )

wherein

R¹ is H, d_₆alkyl, Cι.₆haloalkyl, d_₆alkoxy, Cι.₆thioalkyl, cyano, halo, C₃.₇cycloalkyl, -Cι-₆alkylene-C₃-₇cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl;

R⁸ is O-Cι.₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C; X¹ is N;

Y¹ is N;

Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -d-4- alk(en)ylene-CN, halo, Cι.₆alkyl, C₂.₆alkenyl, C₃_ ₆alkynyl, Cι.₆haloalkyl, aryl, -Cι_ alk(en)ylene-aryl, -

Ci_₄alk(en)ylene-heterocyclo, heterocyclo, ~d_ ₄alk(en)ylene- amino, -C₁.₄alkylene-amino-Cι-₄alkyl, aryl-amino, -amino-(Cι.₆alk(en)yl)ι-₂, -amino-aryl, - amino-heterocyclo, Cι_₆alkoxy, -O-aryl and -O- heterocyclo;

Z¹ is C(O); and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_ alkyl, Cι_₄alkoxy, Cι_₆thioalkyl, C_\. ₄haloalkyl, halogen, N(C C alkyl)₂ and CN. According to another embodiment of a third aspect of the present invention are provided processes for preparing compounds of Formula (Z')

wherein

R¹ is H, Cι_₆alkyl, Cι_₆haloalkyl, Cι.₆alkoxy, Ci.₆thioalkyl, cyano, halo, C₃.₇cycloalkyl, -d. alkylene-C₃.. cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl; R⁸ is O-d.₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C;

X¹ is N;

Y¹ is N; Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -Cι-₄- alk(en)ylene-CN, halo, d.₆alkyl, C₂.₆alkenyl, C₃. βalkynyf, Ci.₆haloalkyl, aryl, -C₁. alk(en)ylene-aryl, - d_ alk(en)ylene-heterocyclo, heterocyclo, -d_ ₄alk(en)ylene- amino, aryl-amino, -amino-(C₁.₆alk(en)yl)₁.₂, -amino-aryl, - amino-heterocyclo, -O-aryl and -O- heterocyclo;

Z¹ is C(O); and Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_₄alkyl, Cι.₄alkoxy, d_₆thioalkyl, d. ₄haloalkyl, halogen, N(C₁-C alkyl)₂ and CN;

comprising reacting a compound of Formula (X')

HZ. '-" M, °" wherein

Z, Z¹ and Y² are defined as for Formula (Z');

with a compound of Formula (T FF ')

wherein

R¹, R⁸ , X, Y, X¹ and Y¹ are defined as for Formula (Z'); in the presence of a suitable base and polar aprotic solvent to yield a compound of Formula (Y')

wherein R¹, R⁸ , X, Y, X¹, Y¹, Y², Z¹ and Z are defined as for Formula (Z'); and reacting said compound of Formula (Y') with a high-boiling point polar aprotic solvent and a suitable silver salt under suitably high temperature. According to another embodiment of a third aspect of the present invention are provided compounds of Formula (AA')

wherein

R¹ is H, C_halky!, Cι-₆haloalkyl, d-₆alkoxy, Cι-₆thioalkyl, cyano, halo, C₃.₇cycloalkyl, -d-ealkylene-d.-zcycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl; R⁸ is O-Cι.₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C;

X¹ is N;

Y¹ is N; Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -d-4- alk(en)ylene-CN, halo, d-βalkyl, C₂-6alkenyl, C₃. ₆alkynyl, d_₆haloalkyl, aryl, -d. alk(en)ylene-aryl, - Cι_₄alk(en)ylene-heterocyclo, heterocyclo, -Cι_ ₄alk(en)ylene- amino, aryl-amino, -amino-(d.₆alk(en)yl)ι-2, -amino-aryl, - amino-heterocyclo, d_₆alkoxy, -O-aryl and -O- heterocyclo;

Z¹ is CR⁷; wherein R⁷ is chloro or bromo; and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_₄alkyl, d_ alkoxy, Cι_₆thioalkyl, Ci. ₄haloalkyl, halogen, N(Cι-C alkyl)₂ and CN.

According to another embodiment of a third aspect of the present invention are provided processes for preparing compounds of Formula (AA')

wherein

R¹ is H, Cι-₆alkyl, Cι.₆haloalkyl, Cι_₆alkoxy, Cι.₆thioalkyl, cyano, halo, C₃- cycloalkyl, -d-₆alkylene-C₃.₇cycloalkyl, C₂.₆alkenyl or C₃_₆alkynyl;

R⁸ is O-Cι. alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C; X¹ is N;

Y¹ is N;

Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -d-₄- alk(en)ylene-CN, halo, d_₆alkyl, C₂.₆alkenyl, C₃. ₆alkynyl, d.₆haloalkyl, aryl, -Cι.₄alk(en)ylene-aryl, -

Cι. alk(en)ylene-heterocyclo, heterocyclo, -Cι_ alk(en)ylene- amino, aryl-amino, -amino^d-eal ^enjyl)_!^, -amino-aryl, - amino-heterocyclo, Cι_₆alkoxy, -O-aryl and -O- heterocyclo;

Z¹ is CR⁷; wherein R⁷ is chloro or bromo; and Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι. alkyl, Cι_ alkoxy, Cι.₆thioalkyl, d_ haloalkyl, halogen, N(Cι-C₄alkyl)₂ and CN;

comprising reacting a compound of Formula (Z')

wherein R¹, R⁸ , X, Y, X¹, Y¹, Y², and Z are defined as for Formula (AA'); and

Z¹ is C(O); with phosphoryl trichloride or phosphoryl tribromide, neat or with a suitable solvent and without a base or with a suitable base.

Other embodiments of the present invention may comprise a suitable combination of two or more of the embodiments and/or aspects disclosed herein.

Yet other embodiments and aspects of the invention will be apparent according to the description provided below.

Detailed Description of the Invention The description of the invention herein should be construed in congruity with the laws and principals of chemical bonding. An embodiment or aspect which depends from another embodiment or aspect, will describe only the variables having values and provisos that differ from the embodiment or aspect from which it depends. As used herein, "aryl" or "ar-" includes phenyl or napthalenyl. As used herein, "heterocyclic" or "heterocyclo" includes both heteroaryl and heteroalicyclic. "Heteroaryl" includes but is not limited to furyl, thienyl, benzothienyl, thiazolyl, imidazolyl, oxazolyl, oxadiazolyl, thiadiazolyl, benzthiazolyl, triazolyl, tetrazolyl, isoxazolyl, isothiazolyl, pyrrolyl, pyranyl, tetrahydropyranyl, pyrazolyl, pyridyl, pyrimidinyl, quinolinyl, isoquinolinyl, purinyl, carbazolyl, benzoxazolyl, benzimidazolyl, indolyl, isoindolyl or pyrazinyl. "Heteroalicyclic" includes but is not limited to azetidinyl, piperidyl, piperazinyl, imidazolinyl, thiazolidinyl, 3-pyrrolidin-l-yl, morpholinyl, thiomorpholinyl or tetrahydropyranyl. "Heteroalicyclic" further includes moieties otherwise heteroaromatic but for the addition of one or more hydrogen atoms, e.g., dihydropyridine. As used herein, "halo" or "halogen" includes fluoro, chloro, bromo and iodo and further means one or more of the same or different halogens may be substituted on a respective moiety.

Unless specificied otherwise, alkyl, alkenyl and alkynyl may be branched or straight chained. As used herein, "alk(en)yl" or "alk(en)ylene" includes alkyl or alkenyl groups. Alkenyl and alkynyl groups may contain one or more double or triple bonds respectively. Where a range of carbon atoms is designated, e.g., C_\. alk(en)ylene, alkenyl groups it is understood that according to the principals of chemical bonding must have at least two carbons in length.

It is to be understood that the present invention may include any and all possible stereoisomers, geometric isomers, diastereoisomers, enantiomers, anomers and optical isomers, unless a particular description specifies otherwise.

The compounds of this invention may exist in the form of pharmaceutically acceptable salts. Such salts may include addition salts with inorganic acids such as, for example, hydrochloric acid and sulfuric acid, and with organic acids such as, for example, acetic acid, citric acid, methanesulfonic acid, toluenesulfonic acid, tartaric acid and maleic acid. Further, in case the compounds of this invention contain an acidic group, the acidic group may exist in the form of alkali metal salts such as, for example, a potassium salt and a sodium salt; alkaline earth metal salts such as, for example, a magnesium salt and a calcium salt; and salts with organic bases such as a triethylammonium salt and an arginine salt. The compounds of the present invention may be hydrated or non-hydrated.

The compounds of this invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixirs, tinctures, suspensions, syrups and emulsions. The compounds of this invention may also be administered intravenously, intraperitoneally, subcutaneously, or intramuscularly, all using dosage forms well known to those skilled in the pharmaceutical arts. The compounds can be administered alone, but generally will be administered with a pharmaceutical carrier selected upon the basis of the chosen route of administration and standard pharmaceutical practice. Compounds of this invention can also be administered in intranasal form by topical use of suitable intranasal vehicles, or by transdermal routes, using transdermal skin patches. When compounds of this invention are administered transdermally the dosage will be continuous throughout the dosage regimen.

Compounds of the present invention may be used for the treatment of a variety of conditions including depression, anxiety, affective disorders, eating disorders and obesity (see Peripheral administration of CRF and urocortin: effects on food intake and the HPA axis in the marsupial Sminthopsis crassicaudata. Hope, P. J.; Turnbull, H; Farr, S.; Morley, J. E.; Rice, . C; Chrousos, G. P.; Torpy, D. J.; Wittert, G. A. Department of Medicine, University of Adelaide, Royal Adelaide Hospital, South Australia, Australia. Peptides (N. Y.) (2000), 21(5), 669-677), sudden death due to cardiac disorders (see Use of corticotropin releasing factor (CRF) antagonists to prevent sudden death. Fossa, Anthony Andrea. (Pfizer Products Inc., USA). Eur. Pat. Appl. (2000), EP 1040831 A2), post-traumatic stress disorder, headache, post-operative stress (see WO 0158489 Al), drug addiction, iritable bowel syndrome (see Stress and the gastrointestinal tract HI. Stress-related alterations of gut motor function: role of brain corticotropin-releasing factor receptors. Tache Y; Martinez V; Million M; Wang L CURE: Digestive Diseases Research Center, Department of Veterans Affairs Greater Los Angeles Healthcare System, Bldg. 115, Rm. 203, 11301 Wilshire Blvd., Los Angeles, CA 90073, USA. AMERICAN JOURNAL OF PHYSIOLOGY. GASTROINTESTINAL AND LIVER PHYSIOLOGY (2001 Feb), 280(2), G173-7; Role of CRF receptor 1 in central CRF-induced stimulation of colonic propulsion in rats. Martinez, V.; Tache, Y. Digestive Disease Division and Brain Research Institute, Department of Medicine, CURE: Digestive Diseases Research Center, Veterans Administration Greater Los Angeles Healthcare System, University of California at Los Angeles, Los Angeles, CA, USA. Brain Res. (2001), 893(1,2), 29-35; and Peripheral corticotropin- releasing factor and stress-stimulated colonic motor activity involve type 1 receptor in rats. Maillot, Celine; Million, Mulugeta; Wei, Jen Yu; Gauthier, Ariane; Tache, Yvette. Digestive Diseases Research Center, VA Greater Los Angeles Healthcare System, Department of Medicine, Division of Digestive Diseases, and Brain

Research Institute, University of California School of Medicine, Los Angeles, CA, USA. Gastroenterology (2000), 119(6), 1569-1579), hypertension (see Combinations of CRF antagonists and renin-angiotensin system inhibitors. Fossa, Anthony Andrea. (Pfizer Products Inc., USA). Eur. Pat. Appl. (2000), 21 pp. and Antalarmin blockade of corticotropin releasing hormone-induced hypertension in rats. Briscoe, R. J.; Cabrera, C. L.; Baird, T. J.; Rice, K. C; Woods, J. H. Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA. Brain Res. (2000), 881(2), 204-207), syndrome X (also known as metabolic syndrome, plurimetabolic syndrome or insulin resistance syndrome) (see EP1 097 709 A2), inflammatory disorders and stress-induced immune suppression (see Stress, corticotropin-releasing hormone, glucocorticoids, and the immune/inflammatory response: acute and chronic effects. Elenkov, Ilia J.; Webster, Elizabeth L.; Torpy, David J.; Chrousos, George P. Pediatric Endocrinology Section, Developmental Endocrinology Branch, National Institute of Child Health and Human Development, and Inflammatory Joint Diseases Section, Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA. Ann. N. Y. Acad. Sci. (1999), 876(Neuroendocrine Immune Basis of the Rheumatic Diseases), 1-13; Corticotropin- releasing hormone and inflammation. Webster, Elizabeth L.; Torpy, David J.; Elenkov, Ilia J.; Chrousos, George P. Pediatric Endocrinology Section,

Developmental Endocrinology Branch, National Institute of Child Health and Development, National Institutes of Health, Bethesda, MD, USA. Ann. N. Y. Acad. Sci. (1998), 840(Neuroimmunomodulation), 21-32; and Peripheral corticotropin-releasing factor mediates the elevation of plasma IL-6 by immobilization stress in rats. Ando T; Rivier J; Yanaihara H; Arimura A United States- Japan Biomedical Research Laboratories, Tulane University Hebert Center, Belle Chasse, Louisiana 70037-3001, USA AMERICAN JOURNAL OF PHYSIOLOGY (1998 Nov), 275(5 Pt 2), R1461-7), infertility (see Corticotropin- releasing factor (CRF) and stress-related reproductive failure: The brain as a state of the art or the ovary as a novel clue? Nappi, R. E.; Rivest, S. CHUL Research Center, Laval University, PQ, Can. J. Endocrinol. Invest. (1995), 18(11), 872- 80)), stress-induced insomnia and other sleep disorders (see Use of CRF antagonists and related compositions for modifying circadian rhythm and treatment of depression and other conditions. Chen, Yuhpyng Liang. (Pfizer Products Inc., USA). Eur. Pat. Appl. (2001), 29 pp EP 1082960 A2; Middle-Aged Men Show Higher Sensitivity of Sleep to the Arousing Effects of Corticotropin-Releasing Hormone Than Young Men: Clinical Implications. Vgontzas AN, Bixler EO, Wittman AM, Zachman K, Lin HM, Vela-Bueno A, Kales A, Chrousos GP. Sleep Research and Treatment Center, Department of Psychiatry and Department of Health Evaluation Sciences (H.-M.L.), Pennsylvania State University, Hershey, Pennsylvania 17033. J. Clin. Endocrinol. Metab. (2001), 86 (4): 1489-1495; JL-1 is a mediator of increases in slow-wave sleep induced by CRH receptor blockade. Chang, Fang-Chia; Opp, Mark R. Neuroscience Graduate Program, University of Texas Medical Branch, Galveston, TX, USA. Am. J. Physiol. (2000), 279(3, Pt. 2), R793-R802; Blockade of corticotropin-releasing hormone receptors reduces spontaneous waking in the rat. Chang, Fang-Chia; Opp, Mark R. Neuroscience Graduate Program, University of Texas Medical Branch, Galveston, TX, USA. Am. J. Physiol. (1998), 275(3, Pt. 2), R793-R802; Non-peptidic corticotropin-releasing hormone receptor type 1 antagonist reverses restraint stress-induced shortening of sodium pentobarbital-induced sleeping time of rats: evidence that an increase in arousal induced by stress is mediated through CRH receptor type 1. Arai, Keiko; Ohata, Hisayuki; Shibasaki, Tamotsu. Department of Physiology, Nippon Medical School, Tokyo, Japan. Neurosci. Lett. (1998), 255(2), 103-106; Rat strain differences suggest a role for corticotropin-releasing hormone in modulating sleep. Opp, Mark R. Department of Psychiatry and Behavioral Sciences, University of Texas Medical Branch, Galveston, TX, USA. Physiol. Behav. (1997), Volume Date 1998, 63(1), 67-74), seizures (see The effect of 'Astressin', a novel antagonist of corticotropin releasing hormone (CRH), on CRH-induced seizures in the infant rat- comparison with two other antagonists. Baram T Z; Koutsoukos Y; Schultz L; Rivier J Department of Pediatrics, University of California, Irvine 92717, USA MOLECULAR PSYCHIATRY (1996 Jul), 1(3), 223-6; and Astressin, a novel and potent CRF antagonist, is neuroprotective in the hippocampus when administered after a seizure. Maecker H; Desai A; Dash R; Rivier J; Vale W; Sapolsky R Department of Biological Sciences, Stanford University, CA 94305, USA BRAIN RESEARCH (1997 Jan 2), 744(1), 166-70), epilepsy (see Infantile spasms. Hypothesis-driven therapy and pilot human infant experiments using corticotropin- releasing hormone receptor antagonists. Baram, Tallie Z.; Mitchell, Wendy G.; Brunson, Kristen; Haden, Elizabeth. Department Anatomy/Neurobiology, Univ. California Irvine, Irvine, CA, USA. Dev. Neurosci. (Basel) (1999), 21(3-5), 281-289; and The pro-con vulsant actions of corticotropin-releasing hormone in the hippocampus of infant rats. Hollrigel, G. S.; Chen, K.; Baram, T. Z.; Soltesz, I. Department of Anatomy and Neurobiology, University of California, Irvine, CA, USA. Neuroscience (Oxford) (1998), 84(1), 71-79), stroke and cerebral ischemia (see Neuroprotection by corticotropin releasing factor during hypoxia in rat brain. Fox M W; Anderson R E; Meyer F B Department of Neurosurgery, Mayo Clinic, Rochester, MN 55905. STROKE (1993 Jul), 24(7), 1072-5; discussion 1075-6; Neuroprotective effects of corticotropin-releasing factor receptor antagonists. Loddick, S. A.; Chalmers, D. T.; Yatsushiro, K.; McCulloch, J.; Foster, A. C; Rothwell, N. J.; De Souza, E. B. Neurocrine Biosciences, Inc., San Diego, CA, USA. Editor(s): Krieglstein, Josef. Pharmacol. Cereb. Ischemia 1998, [Int. Symp.], 7th (1999), Meeting Date 1998, 371-378. Publisher: Medpharm Scientific Publishers, Stuttgart, Germany CODEN: 68OZA5 Conference; Corticotropin releasing factor antagonist reduces ischemic hippocampal neuronal injury. Lyons, Mark K.; Anderson, Robert E.; Meyer, Fredric B. Mayo Clin., Mayo Grad. Sch. Med., Rochester, MN, USA. Brain Res. (1991), 545(1-2), 339-42; Focal cerebral ischemia induces CRH mRNA in rat cerebral cortex and amygdala. Wong M L; Loddick S A; Bongiorno P B ; Gold P W; Rothwell N J; Licinio J Clinical Neuroendocrinology Branch, NIMH, NIH, Bethesda, Maryland 20892-1284, USA NEUROREPORT (1995 Sep 11), 6(13), 1785-8; ) traumatic brain injury (see Evidence for the involvement of corticotrophin-releasing hormone in the pathogenesis of traumatic brain injury. Roe S Y; McGowan E M; Rothwell N J School of Biological Sciences, University of Manchester, UK EUROPEAN JOURNAL OF NEUROSCIENCE (1998 Feb), 10(2), 553-9; The effects of human corticotrophin releasing factor on motor and cognitive deficits after impact acceleration injury. Beaumont, Andrew; Marmarou, Christina; Marmarou, Anthony. Division of Neurosurgery, Department of Physiology, Medical College of Virginia, Richmond, VA, USA. Neurol. Res. (2000), 22(7), 665-673) and yet other disorders requiring neuroprotection, drug or alcohol withdrawal symptoms, other disorders including tachycardia, congestive heart failure, osteoporosis, premature birth, psychosocial dwarfism, ulcer, diarrhea and post-operative ileus (see New uses for heterocyclic corticotropin-releasing factor (CRF) antagonists in treating cardiovascular diseases, osteoporosis, ulcers, and other disorders. Chen, Yuhpyng Liang; Fossa, Anthony Andrea. (Pfizer Inc., USA). Eur. Pat. Appl. (1997), 15 pp. EP 773023 Al) and yet other conditions the treatment of which can be effected by the antagonism of the CRF-1 receptor by the administration of pharmaceutical compositions comprising compounds of the present invention as described herein.

The dosage and dosage regimen and scheduling of a compounds of the present invention must in each case be carefully adjusted, utilizing sound professional judgment and considering the age, weight and condition of the recipient, the route of administration and the nature and extent of the disease condition. In accordance with good clinical practice, it is preferred to administer the instant compounds at a concentration level which will produce effective beneficial effects without causing any harmful or untoward side effects. Compounds of the present invention may be synthesized according to the general schemes provided below. Variables corresponding to compounds of Formula (I) have been introduced in the schemes below at particular instances to further depict how said compounds may be synthesized. Variables provided in the schemes below are defined in accordance with the description of compounds of Formula (I) unless otherwise specified. Where a variable has been further defined in any one scheme below, said variable should assume the same values in subsequent schemes unless yet further defined. The definitions of compounds in the schemes below are not intended to narrow the scope of compounds described by Formula (I). Moreover, the schemes provided herein may be modified in a manner apparent to one skilled in the art to describe additional processes for making compounds of the present invention. Scheme 1

Inc T

(G) (H)

Scheme 2

Scheme 3

e

Scheme 4

Scheme 6

(EE)

(AA),(BB),(CC),or(DD) Scheme 7

Scheme 8

1.IMBH₃-THF _i10X_LG ^{R NH;} _„,'₀ ^uΛ" "„ ^CHJ^O N,R^{4 H}

" 3. t-butylpyrocarbonate " R^10' N

(MM) H HCI

4.4M HCI/dioxane

(NN) (OO) wherein R¹⁰-CH₂ = R³ LG = leaving group Scheme 9

(TT) (UU) (VV)

Scheme 10

Scheme 11

(III) (JJJ)

(KKK) (LLL) (MMM)

Scheme 13

R and R are the same

(QQQ)

Scheme 14

(NNN) (RRR)

(SSS)

(TTT)

(WWW)

(UUU) (VW)

Other suitable means of synthesizing said compounds may also be available. More detailed descriptions of synthesizing compounds of the present invention are also provided as follows:

General. 1H and ¹³C NMR spectra in CDC1₃ were run on a Bruker 500 or 300 MHz instrument and chemical shifts were reported in ppm (δ) with reference to (CH₃)₄Si. All evaporations were carried out under reduced pressure. Unless otherwise stated, LC/MS analyses were carried out on a Shimadzu instrument using a YMC C18 column (3 x 50 mm) employing a 2 min linear gradient of 0% tol00% solvent B in A in a 3 min run. For LC MS and for Shimadzu Preparative HPLC system, Solvent A- was:10% methanol/90% water/0.1% trifluoroacetic acid, and solvent B was 90% methanol/10% water/0.1% trifluoroacetic acid with a UV detector set at 220 nm.

The following Intermediates 1-5 may be used to synthesize Examples 1-26.

Intermediate 1

N¹-(2,4.6-Trimethyl-phenyI)-ethane-l,2-diamine, scheme 3: (M)

To a solution of 2,4,6-trimethylaniline (100. g, 0.740 mol) in anhydrous toluene (600 mL) was added 2-bromoethylamine hydrobromide (75.8 g, 0.370 mol). The flask containing the reaction mixture was fitted with a Dean-Stark trap/reflux condenser assembly. The reaction mixture was heated at reflux temperature for 5 h, during which time the mixture solidified. Upon cooling to room temperature, the solidified mass was treated with water (240 mL), toluene (160 mL), and 50% aqueous OH (80 mL). The phases were separated, and the aqueous portion was saturated with NaCl and extracted with toluene (2 X 200 mL). The combined organic portions were washed with brine, dried over anhydrous Na₂SO₄, filtered, and concentrated under reduced pressure to remove the solvent. Vacuum distillation (2 mm Hg) afforded 42.4 g of a light yellow liquid, which was 92% pure based on 1H NMR. Eight per cent of the material was unreacted

2,4,6-trimethylaniline. 1H NMR (CDC1₃, 300 MHz) δ 6.83 (s, 2H), 3.00 - 2.96 (m,

2H), 2.92 - 2.88 (m, 2H), 2.28 (s, 6H), 2.23 (s, 3H), 2.21 (s, IH), 2.16 (s, 2H). LC/MS: t_R = 0.87 min., (MH⁺) = 179.19.

Intermediate 2

l-(2,4,6-Trimethyl-phenyl)-4,5-dihydro-lH^r-imidazol-2-ylamine, scheme 3: (N)¹

A solution of cyanogen bromide (1.8 g, 18.5 mmol) in anhydrous ethanol (3 mL) was

added at 0°C to a solution of N¹-(2,4,6-trimethyl-phenyl)-ethane-l,2-diamine (3.0 g,

16.9 mmol) in anhydrous ethanol (9 mL) under nitrogen. The reaction mixture was

warmed up to room temperature for 10 min, then was heated at 155 °C for 40 min

with a flow of nitrogen to remove ethanol. Upon cooling to r.t., the resulting solids were transferred to a separatory funnel via dichloromethane (70 mL), and washed

sequentially with 1 N sodium hydroxide (2 x 35 mL), water and brine. The organic

layer was dried over anhydrous sodium sulfate and solvents were removed in vacuo to afford the title compound as a pale white solid (3.08 g, 90% yield). The solids were used for the next step without further purification. 1H NMR (CDC1₃, 300 MHz)

δ 6.70 (s, 2H), 3.46 (s, 4H), 2.06 (s, 3H), 1.99 (s, 6H); ¹³C NMR (CDCl_3j 75 MHz) δ 160.1, 138.2, 137.8, 132.2, 129.5, 48.8, 43.5, 20.8, 17.5. LC/MS: t_R = 0.99 min., (MH*) = 204.12.

Intermediate 3

3-Ethoxycarbonylmethyl-l-(2,4,6-trimethyl-phenyl)-2-aminoimidazolium bromide, scheme 3: (O)

To a mixture of l-(2,4,6-trimethyl-phenyl)-imidazolidin-2-ylideneamine (3.00 g, 0.0148 mol) and aluminum tri-tert-butoxide (1.0 g, 0.0041 mol) in dimethylformamide (15 mL) was added ethyl bromoacetate (1.65 mL, 2.48 g,

0.00148 mol). The reaction mixture was allowed to stir at room temperature for 1 h, after which LC-MS indicated a 4:1 ratio of desired product to starting material. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure to give a pale orange-yellow solid, which was then treated twice with toluene to azeotropically remove any water. The solid was triturated with toluene, collected by filtration, and placed under high vacuum for 6 h. 1H NMR (CDC1₃, 300

MHz) δ 7.01 (s, 2H), 4,87 (s, 2H), 4.29 (q, J = 7 Hz, 2H), 3.96 - 3.89 (m, 4H), 2.32

(s, 3H), 2.25 (s, 6H), 1.34 (t, J = 7 Hz, 3H). LC/MS: t_R = 0.92 min., (MEf ) = 290.43. Intermediate 4

2-Methyl-7-(2,4,6-trimethvI-phenyI)-6,7-dihvdro-5H-imidazori,2-cylimidazole-3-

carboxylic acid ethyl ester, (scheme 3: (P)² A mixture of 3-ethoxycarbonylmethyl-l-(2,4,6-trimethyl-phenyl)-2- aminoimidazolium bromide (1.0 g, 2.7 mmol), sodium acetate (0.55 g, 6.75 mmol)

and acetic anhydride (5.0 mL) was heated at 160 °C for 12 hr. Upon cooling, the

mixture was poured into a flask containing ice. While stirring, excess sodium bicarbonate was added to the above mixture in small portions, and the resulting mixture was stirred at room temperature for 6 hr. Then, the mixture was extracted

with dichloromethane (2 x 40 mL). The organic extracts were washed with water

and dried over anhydrous sodium sulfate. Solvents were removed in vacuo and the residue was subjected to chromatography using ethyl acetate/hexanes (1:4) as eluent to afford the title compound as a light yellow oil which solidified upon cooling

(0.344 g, 41% yield). 1H NMR (CDC1₃, 300 MHz) δ 6.89 (s, 2H), 4.32 (q, J = 7.1

Hz, 2H), 4.36 - 4.26 (m, 2H), 4.15 - 4.08 (m, 2H), 2.39 (s, 3H), 2.26 (s, 3H), 2.20 (s, 6H), 1.35 (t, J = 7.1 Hz, 3H). Mass spec: 314.15 (MH ). Intermediate 5

2-Ethyl-7-(2.4.6-trimethyI-phenvI)-6,7-dihydro-5H^r-imidazoπ,2-αlimidazole-3-

carboxylic acid ethyl ester, scheme 3: (P)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 6.90 (s,

2H), 4.36 (t, J = 8.4 Hz, 2H), 4.30 (q, J = 7.2 Hz, 2H), 4.14 (t, J = 8.4 Hz, 2H), 2.81 (q, J = 7.4 Hz, 2H), 2.26 (s, 3H), 2.21 (s, 6H), 1.36 (t, J = 7.1 Hz, 3H), 1.11 (t, J = 7.5 Hz, 3H). LC/MS: t_R = 1.35 min., (MH⁺) = 328.19.

Example 1

2-MethvI-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazoπ,2-Q;limidazole-3-

carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q)

A solution of trimethyl aluminum (2.0 M in heptane, 2.2 mL, 4.4 mmol) was added to a solution of N-cyclopropylmethyl-N-propylamine (0.63 mL, 4.4 mmol) in

benzene (3 mL) at 0°C. The mixture was warmed up to room temperature and stirred

at this temperature for 1.5 h, and then added to a stirred solution of 2-methyl-7-

(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-irru^azo[l,2-α]imidazole-3-carboxylic acid ethyl ester (0.172 g, 0.55 mmol) in benzene (8.0 mL). The mixture was refluxed for 12 h. Upon cooling at 0°C, 1 N sodium hydroxide (25 mL) was added dropwise to

the above mixture. The mixture was extracted with dicholoromethane (40 mL), and the organic layer was dried over anhydrous sodium sulfate. Solvents were removed in vacuo and the residue was subjected to chromatography using ethyl acetate/hexanes (1:1) as eluent to afford the title compound as a light yellow oil

which solidified upon cooling (0.209 g, 100% yield). 1HNMR (CDC1₃, 300 MHz) δ

; ¹³C NMR (CDC1₃, 75 MHz) δ 163.1, 156.0, 141.0, 136.5, 136.1, 132.7, 128.7,

115.8, 52.6, 50.3, 47.1, 42.1, 20.1, 19.9, 17.3, 14.6, 10.3, 9.2, 2.8. Mass spec: 381.26 (MT ).

Example 2

2-Ethyl-7-(2,4.6-trimethyl-phenyl)-6,7-dihydro-5H-imidazoπ,2- y|imidazole-3-

carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q) Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 6.83 (s,

2H), 4.12 - 4.01 (m, 4H), 3.56 (t, J = 7.1 Hz, 2H), 3.35 (d, J = 6.8 Hz, 2H), 2.42 (q, J = 7.5 Hz, 2H), 2.21 (s, 3H), 2.17 (s, 6H), 1.59 (quintet, J = 7.2 Hz, 2H), 1.11 (t, J = 7.5 Hz, 3H), 0.99 - 0.95 (m, IH), 0.86 (t, J = 7.3 Hz, 3H), 0.51 - 0.48 (m, 2H), 0.17 -

0.13 (m, 2H); ¹³C NMR (CDC1₃, 75 MHz) δ 164.1, 156.9, 147.6, 137.3, 136.9, 133.9,

129.6, 115.6, 53.6, 51.2, 48.1, 42.9, 22.6, 21.0, 20.9, 18.2, 13.7, 11.3, 10.0, 3.75. LC/MS: t_R = 1.36 min., (MH⁺) = 395.27. Example 3

Cyclopropylmethyl-r2-methyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5fl^r-

imidazori,2-«limidazol-3-ylmethyll-propyl-amine, scheme 3: (R)

A solution of Red-Al (3.3 M in toluene, 0.70 mL, 2.33 mmol) was added dropwise to a solution of 2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazo[l,2-

α]imidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide (0.177 g, 0.46

mmol) in toluene (3 mL) at 0°C. After stirring at room temperature for 24 h, the

reaction mixture was cooled to 0°C and I N sodium hydroxide (10 mL) was added

dropwise. The above mixture was extracted with dichloromethane (40 mL), and the organic extracts were washed with water and dried over anhydrous sodium sulfate. Solvents were removed in vacuo to afford the title compound as a light yellow oil which solidified upon cooling (109 mg, 65% yield). The purity of the product was

determined to be 91% by LC/MS. 1H NMR (CDC1₃, 300 MHz) δ 6.85 (s, 2H), 4.09 -

3.96 (m, 4H), 3.45 (s, 2H), 2.44 (t, J = 7.1 Hz, 2H), 2.29 (d, J = 6.5 Hz, 2H), 2.23 (s, 3H), 2.19 (s, 6H), 2.04 (s, 3H), 1.46 (quintet, J = 7.3 Hz, 2H), 1.28 - 1.25 (m, IH), 0.87 (t, J = 7.2 Hz, 3H), 0.49 - 0.46 (m, 2H), 0.09 - 0.06 (m, 2H); ¹³C NMR (CDC1₃,

75 MHz) δ 155.4, 137.1, 136.9, 136.0, 135.0, 129.7, 117.7, 58.5, 55.5, 53.8, 48.0,

42.4, 20.9, 20.3, 18.2, 13.3, 12.0, 8.9, 4.0. Mass spec: 367.24 (MH^"). Example 4

Cvclopropylmethyl-r2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5g-

imidazori,2-α|imidazol-3-ylmethyn-propyl-amine, scheme 3: (R)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 6.86 (s, 2H), 4.13 - 3.97 (m, 4H), 3.47 (s, 2H), 2.45 (t, J = 7.2 Hz, 2H), 2.39 (q, J = 7.6 Hz, 2H), 2.31 (d, J = 6.5 Hz, 2H), 2.24 (s, 3H), 2.19 (s, 6H), 1.48 - 1.42 (m, 2H), 1.32 - 1.26 (m, IH), 1.06 (t, J = 7.4 Hz, 3H), 0.87 (t, J = 7.2 Hz, 3H), 0.50 - 0.46 (m, 2H), 0.09 - 0.07 (m, 2H). Mass spec: 381.28 (MH^1").

Example 5

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazoIe-3- carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t = 1.51 min., (MH*^") = 435.36. Example 6

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazole-3- carboxylic acid propyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t = 1.25 min., (MH^4") = 423.37.

Example 7

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazoπ,2-a1imidazole-3- carboxylic acid cyclopropylmethyl- (3,3,3,2,2-pentafluoro-propyl)-amide, scheme

3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.43 min., (MH*) = 485.35. Example 8

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid cyclopropylmethyl- ( cyclopropylmethyD-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.28 min., (MET*^") = 407.42.

Example 9

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazori,2-a1imidazole-3- carboxylic acid cyclopropylmethyl-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.28 min., (MH^") = 449.37.

Example 10

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazole-3- carboxylic acid cyclopropylmethyl- (ethyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t = 1.41 min., (MH^") = 381.36.

Example 11

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazori,2-alimidazole-3- carboxylic acid dipropyl-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.26 min., (MET^1") = 383.41.

Example 12

2-Ethyl-7-(2.4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazole-3- carboxylic acid propyl-(3,3,3-trifluoropropyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.28 min., (MH^") = 437.33. Example 13

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazole-3- carboxylic acid phenethyl-propyl-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.45 min., (MET^1") 445.37.

Example 14 ^*

2-Ethyl-7-(2,4,6-trimethyI-phenyl)-6,7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid (4-chloro-benzyl)-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.48 min., (MH^1") 519.35. Example 15

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-a1imidazole-3- carboxylic acid butyl-ethyl-amide, scheme 3: (Q) Prepared as described for the example above, except that N-ethylbutylamine was used rather than its HCI salt. LC/MS: t_R = 1.41 min., (MH*) = 383.37.

Example 16

2-Ethyl-7-(2,4,6-trimethyI-phenyl)-6,7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid (2-cyclopropyl-ethyl)-ethyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.38 min., (MET*^") 395.45.

Example 17

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid (2-cycIopropyl-ethyl)-(3,3,3-trifluoro-propyl)-amide, scheme 3:

(Q)

Prepared as described for the example above. LC/MS: t_R = 1.33 min., (Mrl) = 395.45.

Example 18

2-Ethyl-7-(2,4,6-trimethyl-phenyI)-6.7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid benzyl-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t^ = 1.51 min., (MH⁴) 485.39.

Example 19

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazon,2-alimidazole-3- carboxylic acid allyl-propyl-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.31 min., (MET) 381.36.

Example 20

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazon.2-alimidazole-3- carboxylic acid (2-cycIopropyl-ethyl)-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.33 min., (MH⁺) 409.43.

Example 21

2-Ethyl-7-(2.4.6-trimethyI-phenyl)-6,7-dihydro-5H-imidazon.2-a1imidazole-3- carboxylic acid (4-chloro-benzyl)-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.40 min., (MET^1") 465.35. Example 22

2-Ethyl-7-(2,4,6-trimethyI-phenyl)-6,7-dihydro-5H-imidazori,2-a1imidazole-3- carboxylic acid diallylamide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.39 min., (MH ^") 379.40.

Example 23

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazoIe-3- carboxylic acid phenethyI-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.39 min., (MH ^") 499.38. Example 24

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazori,2-a1imidazole-3- carboxylic acid (3-fluoro-benzyl)-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.50 min., (MH^1") 503.17.

Example 25

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazoπ,2-a1imidazole-3- carboxylic acid benzyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.41 min., (MH^1") 431.34. Example 26

2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazole-3- carboxylic acid (3-fluoro-benzyl)-propyl-amide, scheme 3: (Q) Prepared as described for the example above. LC MS: t_R = 1.38 min., (MH*^") 449.35.

The following Intermediates 6-10 may be used to synthesize Examples 27-29.

Intermediate 6

2-Chloro-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide, scheme 3: (K)

To a solution of 2-chloro-4,6-dimethylaniline (0.300 g, 0.00193 mol) in dichloroethane (6 mL) was added chloroacetic anhydride (0.460 g, 0.0027 mol). The reaction was allowed to stir at room temperature for 1 h and was then quenched with saturated aqueous NaHCO and allowed to stir for another 15 min. The reaction mixture was extracted with ethyl acetate (2 X 15 mL), and the combined organic portions were washed sequentially with saturated aqueous NaHCO₃ and brine. After drying over anhydrous Na₂SO₄, the organic portion was concentrated under reduced pressure to give 0.40 g (0.0017 mol, 90%) of white solid. 1H NMR (CDCI₃, 300 MHz) δ 7.94 (br s, IH), 7.12 (s, IH), 6.98 (s, IH), 4.25 (s, 2H), 2.3 (s, 3H), 2.24 (s,

3H). LC/MS: t_R = 1.22 min., (MH^4") = 232.02.

Intermediate 7

2-Azido-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide, scheme 3: (L)

A mixture of 2-Chloro-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide (0.100 g, 0.00043 mol), potassium iodide (0.0072 g, 0.00043 mol), sodium azide (0.056 g, 0.00086 mol), and anhydrous dimethylformamide (7 mL) was heated in a 50°C oil bath for 4 h. Upon cooling to room temperature, the reaction mixture was cooled to 0°C, water (10 mL) was added, and the solid product was collected by suction filtration, washed several times with water, and placed in a vacuum oven set at low heat for 4 h. The dried product amounted to 0.0934 g (0.391 mmol, 91%). 1H NMR

(CDC1₃, 300 MHz) δ 7.70 (br s IH), 7.12 (s, IH), 6.98 (s, IH), 4.2 (s, 2H), 2.3 (s,

3H), 2.23 (s, 3H). LC/MS: t_R = 1.23 min., (MH^1") = 239.06.

N¹-(2-Chloro-4,6-dimethyl-phenyl)-ethane-l,2-diamine, scheme 3: (M) 2-Azido-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide (0.210 g, 0.00126 mol) was dissolved in cold 1.0 M BH₃- tetrahydrofuran (7.6 mL), and the reaction mixture was allowed to stand for approximately 15 min. and was then heated at reflux temperature for 14 h. Upon cooling to room temperature, the reaction was quenched with excess methanol, and the solvents were removed in vacuo. The residue was dissolved in 10 mL 1:1 methanol: 10% aqueous HCI and heated at reflux temperature for 3 h. Upon cooling to room temperature, the reaction solution was basified with 2 N aqueous NaOH and extracted with ethyl acetate (3 X 20 mL). The combined organic portions were washed with water and brine, dried over anhydrous Na₂SO , and concentrated under reduced pressure to give 0.220 g (0.00111 mol, 88%) of pale yellow liquid. 1H-

NMR δ (CDC1₃, 300 MHz) 2.22 (s, 3H), 2.29 (s, 3H), 2.86 (t, 2H), 3.06 (t, 2H), 6.84

(d, IH), 6.99 (d, IH). LC/MS: t_R = 1.90 min., (MET) = 199.08.

Intermediate 9

l-(2-Chloro-4,6-dimethyl-phenyl)-imidazolidin-2-ylideneamine, scheme 3: (N)

Prepared as described for l-(2,4,6-trimethyl-phenyl)-imidazolidin-2-ylideneamine. 1H-NMR δ (CDC1₃, 300 MHz) 2.22 (s, 3H), 2.26 (s, 3H), 3.63 (m, IH), 3.73 (m, 2H),

3.86 (m, IH), 6.07 (br, 2H), 6.96 (s, IH), 7.08 (s, IH). LC/MS: t_R = 0.87 min., (MH^4") = 224.15.

Intermediate 10

3-EthoxycarbonylmethyI-l-(2-chloro-4,6-dimethyl-phenyl)-2-aminoimidazolium bromide, scheme 3: (O)

Prepared as described for 3-ethoxycarbonylmethyl-l-(2,4,6-trimethyl-phenyl)-2- aminoimidazolium bromide. LC/MS: t_R = 0.98 min., (MH^4") = 310.17.

Intermediate 11

7-(2-Chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid ethyl ester, scheme 3: (P) Prepared as described for 2-ethyl-7-(2,4,6-trimethylphenyl)-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester. LC/MS: t_R = 1.33 min., (MH^4") = 348.17.

7-(2-Chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid cyclopropyImethyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q) Prepared as described for 2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)- amide. LC/MS: t_R = 1.36 min., (MH^4") = 455.19.

Example 28

7-(2-Chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazoπ,2- alimidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.41 min., (MH^4") 415.24.

Example 29

7-(2-ChIoro-4,6-dimethyl-phenyl)-2-ethyl-6.7-dihydro-5H-imidazon,2 alimidazoIe-3-carboxylic acid cvclopropylmethyI-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.38 min., (MH^4") = 469.20. The following Intermediates 12-17 may be used to synthesize Examples 30-33.

Intermediate 12

2-Chloro-N-(2,4-dichIoro-6-methyl-phenyl)-acetamide, scheme 3: (K)

Prepared as described for 2-chloro-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide. Mass spec: 253.94 (MH^4").

Intermediate 13

C

2-Azido-N-(2,4-dichloro-6-methyl-phenyl)-acetamide, scheme 3: (L)

Prepared as described for 2-azido-N-(2-chloro-4,6-dimethyl-phenyl)-acetamide.

N¹-(2,4-Dichloro-6-methyl-phenyl)-ethane-l,2-diamine, scheme 3: (M)

Prepared as described for N¹-(2-chloro-4,6-dimethyl-phenyl)-ethane-l,2-diamine. 1H-

NMR δ (CDC1₃, 300 MHz) 2.28 (s, 3H), 2.84 (t, 2H), 3.07 (t, 2H), 6.98 (d, IH), 7.15

(d, IH); Mass spec: 219.04 (MH^4"). Intermediate 15

l-(2,4-Dichloro-6-methyl-phenyl)-imidazolidin-2-ylideneamine, scheme 3: (N) Prepared as described for l-(2-chloro-4,6-dimethyl-phenyl)-imidazolidin-2- ylideneamine. Mass spec: 244.03 (MH^4").

Intermediate 16

3-Ethoxycarbonylmethyl-l-(2,4-chIoro-6-methyl-phenyl)-2-aminoimidazolium bromide, scheme 3: (O)

Prepared as described for 3-ethoxycarbonylmethyl-l-(2-chloro-4,6-dimethyl-phenyl)- 2-aminoimidazolium bromide. LC/MS: t_R = 1.12 min., (MH^4") = 410.05.

Intermediate 17

^clγV^cl

7-(2,4-Dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazon.2- alimidazole-3-carboxylic acid ethyl ester, scheme 3: (P)

Prepared as described for 7-(2-chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester. LC/MS: t_R = 1.39 min., (MH^4") = 368.16.

Example 30

7-(2,4-Dichloro-6-methyl-phenyl)-2-ethvI-6,7-dihydro-5H-imidazoπ,2- alimidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q)

Prepared as described for 7-(2-chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)- amide. LC/MS: t_R = 1.46 min., (MH⁴) = 475.19.

Example 31

7-(2,4-Dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazon,2- alimidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.42 min., (MH^4") = 435.18.

Example 32

7-(2,4-Dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazon,2- alimidazole-3-carboxylic acid cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)- amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t = 1.50 min., (MH^4-) = 525.13.

Example 33

7-(2,4-Dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid propyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3:

(Q) Prepared as described for the example above. LC/MS: t_R = 1.41 min., (MH⁴ = 463.19.

The following Intermediates 18-23 may be used to synthesize Examples 34-40.

Intermediate 18

N-(2-Bromo-4-isopropyl-phenyl)-2-chloro-acetamide, scheme 3: (K)

Prepared as described for 2-chloro-N-(2,4-dichloro-6-methyl-phenyl)-acetamide. Mass spec: 291.97 (MH^4").

Intermediate 19

2-Azido-N-(2-bromo-4-isopropyI-phenyl)-acetamide, scheme 3: (L) Prepared as described for 2-azido-N-(2,4-dichloro-6-methyl-phenyl)-acetamide.

Intermediate 20

N¹-(2-Bromo-4-isopropyl-phenyl)-ethane-l,2-diamine, scheme 3: (M)

Prepared as described for N¹-(2,4-dichloro-6-methyl-phenyl)-ethane-l,2-diamine. Mass spec: 270.08 (MET").

Intermediate 21

l-(2-Bromo-4-isopropyl-phenyl)-imidazolidin-2-ylideneamine, scheme 3: (N)

Prepared as described for l-(2,4-dichloro-6-methyl-phenyl)-imidazolidm-2- ylideneamine. Mass spec: 284.09 (MH^4").

Intermediate 22

2-Amino-3-(2-bromo-4-isopropyl-phenyl)-l-ethoxycarbonylmethyl-4,5-dihydro- 3H-imidazol-l-ium; bromide, scheme 3: (O)

Prepared as described for 3-ethoxycarbonylmethyl-l-(2,4-chloro-6-methyl-phenyl)-2- aminoimidazolium bromide. LC/MS: t_R = 1.29 min., (MH^4") = 368.20. Intermediate 23

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazori,2- alimidazole-3-carboxylic acid ethyl ester, scheme 3: (P)

Prepared as described for 7-(2,4-dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester. LC/MS: t_R = 1.46 min., (MET^4") = 408.23.

Example 34

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid cvclopropylmethyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q) Prepared as described for 7-(2,4-dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l ,2-a]imidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)- amide. LC/MS: t_R = 1.58 min., (MH^4") = 513.15. Example 35

7-(2-Bromo-4-isopropyl-phenyI)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.47 min., (MH^4") = 473.21.

Example 36

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazori,2- alimidazole-3-carboxy lie acid propyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3:

(Q)

Prepared as described for the example above. LC/MS: t_R = 1.47 min., (MH^4") = 501.02.

Example 37

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazoIe-3-carboxy lie acid cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)- amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.61 min., (MH^4") = 564.29.

Example 38

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazoIe-3-carboxylic acid cyclobutylmethyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.56 min., (MH^4") = 487.21.

Example 39

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid cyclopropylmethyl-(3,3,3-trifluoro-propyl)-amide, scheme 3: (Q) Prepared as described for the example above. LC/MS: t_R = 1.51 min., (MH^4") = 527.15.

Example 40

7-(2-Bromo-4-isopropyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxyIic acid cyclopropylmethyl-ethyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.43 min., (MH^4") = 459.18.

The following Intermediates 24-29 may be used to synthesize Examples 41-49. Intermediate 24

N-(2-bromo-4,6-dimethyl-phenyl)-2-chloro-acetamide, scheme 3: (K)

Prepared as described for 2-chloro-N-(2,4-dichloro-6-methyl-phenyl)-acetamide. Mass spec: 277.95 (MH^4").

Intermediate 25

2-Azido-N-(2-bromo-4,6-dimethyl-phenyl)-acetamide, scheme 3: (L) Prepared as described for 2-azido-N-(2,4-dichloro-6-methyl-phenyl)-acetamide.

Intermediate 26

N¹-(2-bromo-4,6-dimethyl-phenyl)-ethane-l,2-diamine, scheme 3: (M) Prepared as described for N¹-(2,4-dichloro-6-methyl-phenyl)-ethane-l,2-diamine. 1H

NMR δ (CDCI₃, 300 MHz) 2.22 (s, 3H), 2.31 (s, 3H), 2.87 (t, 2H), 3.04 (t, 2H), 6.88

(d, IH), 7.17 (d, IH). Mass spec: 245.11 (MH^4").

Intermediate 27

l-(2-Bromo-4,6-dimethyl-phenyl)-imidazolidin-2-ylideneamine, scheme 3: (N)

Prepared as described for l-(2,4-dichloro-6-methyl-phenyl)-imidazolidin-2- ylideneamine. LC/MS: t_R = 0.91 min., (MH^4") = 270.08.

Intermediate 28

2-Amino-3-(2-bromo-4,6-dimethyl-phenyl)-l-ethoxycarbonylmethyI-4,5- dihydro-3H-imidazoI- 1-ium bromide, scheme 3: (O) Prepared as described for 3-ethoxycarbonylmethyl- 1 -(2,4-chloro-6-methyl-phenyl)-2- aminoimidazolium bromide. LC/MS: tR = 1.03 min., (MH^1") = 356.26.

Intermediate 29

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazon,2- alimidazole-3-carboxylic acid ethyl ester, scheme 3: (P)

Prepared as described for 7-(2,4-dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester. LC/MS: t_R = 1.33 min., (MH^4") = 394.31.

Example 41

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazon,2- alimidazole-3-carboxylic acid phenethyl-propyl-amide, scheme 3: (Q)

Prepared as described for 7-(2,4-dichloro-6~methyl-phenyl)-2-ethyl-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)- amide. LC/MS: t_R = 1.42 min., (MH^1") = 511.35.

Example 42

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyI-6,7-dihvdro-5H imidazon,2- alimidazole-3-carboxylic acid cyclobutylmethyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.68 min., (MH^4") = 475.21.

Example 43

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazole-3-carboxylic acid cyclobutylmethyl-ethyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t = 1.58 min., (MH^4") = 461.35.

Example 44

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihvdro-5H-imidazoπ,2- alimidazole-3-carboxylic acid cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-amide, scheme 3: (Q)

Prepared as described for the example above. LC/MS: t_R = 1.28 min., (MH^4") = 501.16.

Example 45

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- a1imidazole-3-carboxylic acid propyl-(3,3,3-trifluoro-propyl)-amide, scheme 3:

(Q)

Prepared as described for the example above. LC/MS: t_R = 1.60 min., (MH^4") = 503.15.

Example 46

7-(2-Bromo-4,6-dimethyl-phenyl)-2-ethyl-6.7-dihydro-5H-imidazoπ.2- alimidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 3: (Q)

Prepared as described for the example above. LC MS: t_R = 1.56 min., (MH^4") = 461.37.

The following examples 47-48 were prepared from Intermediate 5.

Example 47

4-r2-Ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihvdro-5H-imidazon,2-alimidazol- 3-yll-heptan-4-ol, scheme 11: (DDD)

To a 0°C solution of 2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazo[l,2- a]imidazole-3-carboxylic acid ethyl ester (1 mL of a 0.14M solution in toluene) in tetrahydrofuran (1 mL) was added n-propylmagnesium chloride (0.84 mL of 1.0M in tetrahydrofuran). The resulting solution was removed from the ice bath and allowed to stir for 15 min. It was then heated at reflux for 14h. Upon cooling to room temperature, the reaction solution was quenched with saturated aqueous ammonium chloride, and the phases were separated. The aqueous phase was extracted twice with ether, and the combined organic portions were washed with brine, dried over anhydrous Na₂SO₄, and concentrated under reduced pressure to give a yellow semi- solid (0.0448 g, 86%). LC MS: t_R = 1.58 min., (MET) = 370.31. Example 48

6-Ethyl-5-(l-propyl-but-l-enyl)-l-(2,4,6-trimethyI-phenyl)-2,3-dihydro-lH- imidazori,2-a1imidazole scheme 11: (EEE)

A mixture of 4-[2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H-imidazo[l,2- a]imidazol-3-yl]-heptan-4-ol (0.0444 g, 0.000120 mol) and p-toluenesulfonic acid- H₂O (15 mole %) in toluene (3 mL) was heated at reflux for lh. Upon cooling to room temperature, the solvent was evaporated under reduced pressure, and the residue was partitioned between ether and saturated aqueous sodium bicarbonate. The organic phase was washed with brine, dried over anhydrous Na₂SO₄, and concentrated to give the desired product in quantitative yield. LC-MS indicated the presence of two regioisomers in an approximate ratio of 2:1. LC/MS: t_R = 1.52 min. and 1.63 min., (MH^4") = 352.28.

Example 49

6-Ethyl-5-(l-propyl-butyl)-l-(2,4,6-trimethyl-phenyl)-2,3-dihydro-lH- imidazori,2-a1imidazole, scheme 11: (FFF)

6-Ethyl-5-(l-ρropyl-but-l-enyl)-l-(2,4,6-trimethyl-ρhenyl)-2,3-dihydro-lH- imidazo[l,2-a]imidazole (0.013 g, 0.000037 mol) in anhydrous tetrahydrofuran was treated with cold BH₃-THF (0.15 mL l.OM in tetrahydrofuran), and the mixture was heated at reflux for 1.5 h. The mixture was cooled to 0°C, treated with glacial acetic acid (0.25 mL), heated at reflux for 1.5 h, re-cooled to 0°C, treated with 1.5 mL methanol, and heated again at reflux for lh. Upon cooling to room temperature, the reaction mixture was concentrated under reduced pressure, and the residue was partitioned between 2.5 N NaOH and ether. The organic phase was washed with water and brine, and was then dried over anhydrous Na₂SO and evaporated to give a pale yellow oil. The crude product was chromatographed on silica, eluting with 15% ethyl acetate hexanes to give a glassy solid. LC/MS: t = 1.81 min., (MH^4") = 354.30.

The following examples 50-51 were prepared from Intermediates 11 and 30.

Intermediate 30

4-r7-(2-Chloro-4,6-dimethyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazon,2- a1imidazol-3-γl1-heptan-4-oI, scheme 11: (DDD) Prepared as described for 4-[2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H- imidazo[l,2-a]imidazol-3-yl]-heptan-4-ol. The crude product was chromatographed on silica, eluting with 25% ethyl acetate/hexanes to afford only one of the possible

elimination products. 1H NMR δ (CDC1₃, 300 MHz) 7.12 (s, IH), 7.03 (s, IH), 5.59-

5.34 (t, IH), 4.33-4.08 (br m, 4H), 2.57-2.38 (q, 2H), 2.33 (s, 3H), 2.26(s, 3H), 2.22- 2.15 (t, 2H), 1.74-1.48 (br m, 2H), 1.40-1.33 (q, 2H), 1.25-1.2 (t, 3H), 1.08-1.03 (t, 3H), 0.92-0.88 (t, 3H). LC/MS: t_R = 1.74 min., (MH^4") = 390.25.

Example 50

l-(2-Chloro-4,6-dimethyl-phenyI)-6-ethyl-5-(l-propyl-but-l-enyl)-2,3-dihydro- lH-imidazoπ,2-a1imidazole, scheme 11: (EEE)

Prepared as described for 6-ethyl-5-(l-propyl-but-l-enyl)-l-(2,4,6-trimethyl- phenyl)-2,3-dihydro-lH-imidazo[l,2-a]imidazole. LC/MS: t_R = 1.74 min., (MET") = 372.25.

Example 51

l-(2-Chloro-4,6-dimethyI-phenyl)-6-ethyl-5-(l-propyl-butyl)-2,3-dihvdro-lH- imidazori,2-alimidazole, scheme 11: (FFF)

Prepared as described for 6-ethyl-5-(l-propyl-butyl)-l-(2,4,6-trimethyl-phenyl)-2,3- dihydro-lH-imidazo[l,2-a]imidazole. LC/MS: t_R = 1.74 min., (MH^4") = 374.21.

The following Intermediates 17 and 31 were used to prepare Examples 52 and 53.

Intermediate 31

4-r7-(2,4-Dichloro-6-methyl-phenyl)-2-ethyl-6,7-dihydro-5H-imidazori,2- alimidazol-3-vn-heptan-4-ol, scheme 11: (DDD)

Prepared as described for 4-[2-ethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H- imidazo[l,2-a]imidazol-3-yl]-heptan-4-ol. LC/MS: t_R = 1.74 min., (MH^4") = 410.17.

Example 52

l-(2,4-Dichloro-6-methyl-phenyl)-6-ethyl-5-(l-propyl-but-l-enyl)-2,3-dihydro- lH-imidazori,2-a1imidazole, scheme 11: (EEE)

Prepared as described for 6-ethyl-5-(l-propyl-but-l-enyl)-l-(2,4,6-trimethyl- phenyl)-2,3-dihydro-lH-imidazo[l,2-a]imidazole. LC/MS: t_R = 1.54 min. and 1.65 min., (MET^1") = 392.18.

Example 53

l-(2,4-Dichloro-6-methyl-phenyl)-6-ethyl-5-(l-propyl-butyl)-2,3-dihvdro-lH- imidazori,2-alimidazole, scheme 11: (FFF)

Prepared as described for 6-ethyl-5-(l-propyl-butyl)-l-(2,4,6-trimethyl-phenyl)-2,3- dihydro-lH-imidazo[l,2-a]imidazole. LC/MS: t_R = 1.68 min., (MH⁴) = 394.10.

The following Intermediates 32-43 may be used to synthesize Examples 54-55.

Intermediate 32

(3-Bromo-propyl)-(2,4,6-trimethyl-phenyI)-amine, scheme 7: (FF) To a stirred ice-cold solution of 2,4,6-trimethylaniline (13.5 g, 100 mmol) in dioxane (50 mL) under argon was added 1.2 equivalents of 1.6 M n-BuLi in hexane drop- wise. The brown mixture was allowed to warm up to room temperature during 1 h. At the end 50 mL (approx. 5 equiv.) of 1,3-dibromopropane was added in one lot and stirred for 42 h. Precipitated LiBr was filtered and the volatiles were removed in vacuo. The residue was partitioned between ethyl acetate (300 mL) and water (3x100 mL). The organic layer was dried (Na₂SO₄) and evaporated to give the crude product whose purity by LC-MS analysis was 61%. Silica gel chromatography of the crude product with acetone/hexane (1:9) as eluent gave pure bromopropyl aniline (3.3 g) and an impure fraction which upon crystallization from ethyl acetate hexane gave an additional 2.4 g. (22 % yield). LC/MS: t_R = 1.2 min; [M + H] = 256, 258 (bromine

pattern), 1H NMR (CD₃OD) δ 7.07 (2 H, s), 3.59 (2 H, t, i_c = 6.4 Hz), 3.51 (2 H, t,

i_c = 8.1 Hz), 2.46 (6 H, s), 2.45 - 2.38 (2 H, m), 2.30 (3 H, s).

Intermediate 33

2-Bromo-5-methyl-3-r3-(2,4,6-trimethyl-phenylamino)-propyll-3H-imidazoIe-4- carboxylic acid ethyl ester, scheme 7: GG)

A solution of (1.26 g, 5.4 mmol) bromoimidazole in acetone (43 mL) was combined with (3-bromopropyl)-2,4,6-trimethylaniline (l.lg, 4.25 mmol) and diazabicycloundecene (1.2 equiv). After 96 h, acetone was evaporated and the residue was partitioned between ethyl acetate (250 mL) and water (3 x 50 mL). The organic layer was dried (Na₂SO₄) and evaporated. The residue was purified by silica gel column chromatography using a step gradient of 0% to 70% ethyl acetate in hexane to give 1.1 g (50 % yield) of the required alkylated product. t = 1.3 min.,

MS: [M+H] = 408, 410 (bromine pattern), 1H NMR (CDC1₃) δ 6.82 (2 H, s), 4.45 (2

H, t, i_c = 7.5 Hz), 4.32 (2 H, q, Λi_c = 7.1 Hz), 3.05 (2 H, t, Λi_c = 7.0 Hz), 2.46 (3 H, s), 2.29 (6 H, s), 2.29 (3 H, s), 2.05 (2 H, m), 1.37 (3 H, t, Λi_c = 7.1 Hz). ¹³CNMR

(CDC1₃) δ 160.3, 148.7, 129.7, 124.7, 121.1, 60.6, 46.0, 45.7, 20.6, 18.5, 16.1, 14.3.

A more polar product (0.04g) which corresponded to cyclization product from the N- 3 alkylation of imidazole was also obtained from the later fractions.

Intermediate 34

2-Bromo-5-ethyl-3-r3-(2,4,6-trimethyl-phenylamino)-propyn-3H-imidazole-4- carboxylic acid ethyl ester, scheme 7: (GG)

This compound was prepared from the corresponding 2-bromoimidazole on a 12.9 mmol scale as described in the previous example. Silica gel chromatography of the crude product using a step gradient of 20-70 % ethyl acetate in hexane provided N3- derived cyclization product (0.47g, 11 % yield), t_R = 1.3 min., MS: [M+H] = 342, and Nl-derived alkylation product (2.9g, 54 % yield); LC/MS: t_R = 1.5 min., [M+H]

= 422, 424 (bromine pattern), 1H NMR (CD₃OD) δ 6.74 (2 H, s), 4.40 (2 H, t, Λi_c =

7.6 Hz), 4.31 (2 H, q, Λic = 7.2 Hz), 2.94 (2 H, t, Λi_c = 7.1 Hz), 2.83 (2 H, q, Λi_c = 7.6 Hz), 2.19 (6 H, s), 2.16 (3 H, s), 1.93 (2 H, m), 1.34 (3 H, t, Λi_c = 7.2 Hz), 1.19 (3

H, t, Λic = 7.6 Hz). ¹³CNMR (CD₃OD) δ 161.2, 154.8, 144.0, 132.7, 130.9, 130.5,

126.2, 121.8, 62.0, 47.10, 46.59, 32.2, 23.70, 20.8, 18.7, 14.6, 14.5, 14.3.

2-Bromo-5-trifluoromethyl-3-r3-(2,4,6-trimethyl-phenylamino)-propyl1-3H- imidazole-4-carboxylic acid ethyl ester, scheme 7: (GG)

To a 0.1M dimethylformamide solution containing 5.3 mmol each of the bromoimidazole and bromopropyl aniline was added 1.2 equivalents of Cs₂CO₃. The reaction mixture was stirred at ambient temperature for 96 h. LC-MS indicated approximately 50% conversion to a single alkylated product. Diluted with ethyl acetate (500 mL) and washed with water (3 x 100 mL). Approx. 5 mL ethanol had to be used to break up an emulsion. The ethyl acetate layer was dried (Na₂SO₄), evaporated in vacuo. The crude product was purified by silica gel chromatography with ethyl acetate:hexane (1:9) as eluent. Fractions containing the required compound were combined and evaporated to give 0.5 lg (21 % yield). LC MS: t =

1.5 min., [M+H] = 462, 464 (bromine pattern), 1H NMR (CD₃OD) 6 6.74 (2 H, s),

4.44 (2 H, t, Λi_c = 7.5 Hz), 4.35 (2 H, t, Λi_c = 7.1 Hz), 2.96 (2 H, t, J_vic = 7.1 Hz), 2.20 (6 H, s), 2.15 (3H, s), 1.97 (2 H, m), 1.33 (3 H, t, Λic = 7.1 Hz).

Intermediate 36

2-Methyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazon,2- a]pyrimidine-3-carboxylic acid ethyl ester, scheme 7: (HH) The appropriate Nl-alkylated 2-bromoimidazole (1 g, 2.1 mmol) in sulfolane (50 mL) was heated under argon in the dark with 1.2 equivalents of Ag₂CO₃ for 24h. The reaction mixture was cooled to ambient temperature. Filtered, diluted with water containing 0.1% trifluoroacetic acid to 250 mL. The dark filtrate was applied to an octadecyl silica gel (C18) column (4 x 15 cm) pre-equilibrated with water containing 0.1 % trifluoroacetic acid. Elution with the same solvent was continued until all the sulfolane was removed. The solvent was then changed to methanokO.l % trifluoroacetic acid in water (2:3) collecting 25 mL size fractions which were combined after LC-MS analysis to give 0.9 g of the required product as trifluoroacetate salt of 93 % purity. LC/MS: t_R = 1.1 min., [M+H] = 328, 1H NMR

(CD₃OD) δ 6.94 (2 H, s), 4.29 - 4.24 (4 H, m), 3.47 (2 H, t, Λi_c = 5.5 Hz), 2.27 (3 H,

s), 2.25 (3 H, s), 2.29 (3 H, s), 2.24 (2 H, m), 2.12 (6 H, s), 1.34 (3 H, t, Λi_c = 7.0

Hz). ¹³CNMR (CD₃OD) δ 162.7, 150.3, 147.9, 139.1, 138.8, 137.8, 130.7, 115.2,

60.8, 47.6, 44.4, 23.2, 21.2, 18.3, 15.2, 14.9. Intermediate 37

2-Ethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahvdro-imidazo[l,2-a]pyrimidine- 3-carboxylic acid ethyl ester, scheme 7: (HH) To the Nl-alkylated 2-bromo-4-ethyl imidazole derivative (2.83 g, 6.7 mmol) in sulfolane (67 mL) was added 1.1 equivalents of silver triflate. The resulting solution

was stirred in the dark at 150°C under argon. Within 10 min the solution turned dark and it was stirred for 24 h when LC-MS indicated complete conversion to cyclized product. The reaction mixture was cooled to ambient temperature. Filtered, diluted with water containing 0.1% trifluoroacetic acid to 335 mL and filtered again. The dark filtrate was applied to an octadecyl silica gel (C18) column (4 x 15 cm) pre- equilibrated with water containing 0.1 % trifluoroacetic acid. Elution with the same solvent was continued until all the sulfolane was removed. The solvent was then changed to methanokO.l % trifluoroacetic acid in water (2:3) collecting 25 mL size fractions which were combined after LC-MS analysis to give two major fractions. Cyclization product that was 84 % pure (1.5 g) and pure cyclization product (570 mg). LC/MS : t_R = 1.3 min. , [M+H] = 342,

2-Trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazori,2a1 pyrimidine-3-carboxylic acid ethyl ester, scheme 7: (HH) The appropriate Nl-alkylated-2-bromoimidazole (0.473g, 1.02 mmol) was subjected to silver triflate mediated cyclization in sulfolane (10 mL) as described above except that the reaction was carried out for 48 h. At the end, the mixture was diluted with ethanol (10 mL) filtered through a bed (2 x 4.5 cm) of C18 silica gel and washed with another 50 mL more ethanol. The filtrate was concentrated in vacuo to ca. 20 mL. It was then purified by preparative HPLC using a 20 min. linear gradient (25 min run) of 30-100 % B in A in ten injections. Fractions containing the cyclization product were combined and evaporated. The residue (0.39g) in 20 mL anhydrous ethanol was stirred with (0.168 g, 2 mmol) NaHCO₃ for 1.5 h. Filtered and evaporated to dryness to give 0.23 g (60 % yield) of cyclized product. LC/MS: t_R = 1.8 min., [M+H] = 382.

Intermediate 39

[2-Trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazori,2- a]pyrimidin-3-yl1-methanoI, scheme 7: (II)

The appropriate ethyl ester (0.032g ) in 1 mL of anhydrous tetrahydrofuran was treated with an excess (0.3 mL) of 1 M LiAlBU in tetrahydrofuran at ambient temperature. After lh, 1 M NaOH (5 mL) was carefully added. Most of the tetrahydrofuran was then evaporated. The residue was partitioned between ethyl acetate (2 x 30 mL) and additional 10 mL 1 M NaOH. Organic layer was dried (Na₂SO ) and evaporated. The residue after silica gel chromatography with methanokmethylene chloride (1:99) yielded (0.025g) of alcohol. LC/MS: t_R = 1.0

min., [M+H] = 340, 1H NMR (CD₃OD) δ 6.93 (2 H, s), 4.62 (2 H, s), 4.10 (2 H, t, J_v

= 6.1 Hz), 3.51 (2 H, t, Λi_c = 5.4 Hz), 2.29 (2 H, m), 2.27 (3H, s), 2.13 (6 H, s). Gradient NOES Y experiment revealed NOE between exo methylene group and the methylene at 6 position confirming the regiochemistry.

Intermediate 40

(3-Bromo-propyl)-(2-chloro-4,6-dimethyl-phenyl)-amine, scheme 7: FF)

To a solution of the 2-chloro-4,6-dimethyl aniline (16.9g g, 108 mmol) in 1,4- dioxane (80 mL) was added n-butyl lithium solution (2.5 M in hexanes, 48 mL), dropwise, at 0°C under argon. The reaction mixture was warmed up to rt and stirred for 20 min. 1,3-Dibromopropane (109 g, 543 mmol) was added and the reaction mixture was stirred overnight. The mixture was filtered through celite and concentrated. Purification was carried out by reverse phase chromatography using water, methanol and trifluoroacetic acid to obtain product (20.01 g, 72.5 mmol, 67%)

as brown oil. LC/MS: t_R = 1.5 min. [M+H] 277. 1H NMR (CD₃OD) δ: 7.12 (s, IH),

6.99 (s, IH), 3.52 (t, J = 6.65 Hz, 2H), 3.36 (t, J = 6.75 Hz, 2H), 2.36 (s, 3H), 2.29 (s, 3H), 2.14 (m, 2H).

Intermediate 41

2-Bromo-3-r3-(2-chloro-4,6-dimethyl-phenylamino)-propyll-5-trifluoromethyI- 3H-imidazole-4-carboxylic acid ethyl ester, scheme 7: (GG)

To a solution of the imidazole (5.08 g, 17.7 mmol) in dry dimethylformamide (120 mL) was added the 3-bromopropyl aniline (5.37 g, 19.5 mmol) and cesium carbonate (8.64 g, 26.5 mmol) at RT under argon. The reaction mixture was heated at 55°C overnight, cooled and diluted with ethyl acetate (400 mL). The organic, phase was washed with water (2x), brine and dried (MgSO₄). Purification by silica gel column chromatography using hexanes/ethyl acetate (90:10 to 70:30) afforded product (5.98 g, 12.4 mmol, 70%) as brown oil. LC/MS: t_R= 2.2 min. [M+H] 483. 1HNMR

(CD₃OD) δ: 6.98 (s, IH), 6.86 (s, IH), 4.49 (t, J = 7.55 Hz, 2H), 4.36 (q, J= 7.1 Hz,

2H), 3.10 (t, J= 6.95 Hz, 2H), 2.25 (s, 3H), 2.19 (s, 3H), 2.00 (m, 2H), 1.34 (t, J = 7.1 Hz, 3H). Intermediate 42

l-(2-Chloro-4,6-dimethyl-phenyl)-6-trifluoromethyl-2,3,4,4a-tetrahydro-lH- [l]pyrindine-5-carboxylic acid ethyl ester, scheme 7: HH) To a solution of the alkylated imidazole (5.98 g, 12.4 mmol) in sulfolane (50 mL) was added silver triflate (4.77 g, 18.6 mmol) at rt under argon. The flask was fitted with a reflux condenser and heated at 150°C overnight. The whole setup was covered with aluminum foil to keep the reaction mixture in dark. The reaction mixture was filtered through celite and purified by reverse phase chromatography, using water, methanol and trifluoroacetic acid. Product (3.43 g, 8.54 mmol, 69%) was obtained as

brown solid. LC/MS: to = 2.1 min. [M+H] 402. 1H NMR (CD₃OD) δ: 7.01 (s, IH),

6.92 (s, IH), 4.38 (m, 2H), 4.32 (q, J = 7.15 Hz, 2H), 4.65 (m, 2H), 2.30 (m, 2H), 2.26 (s, 3H), 2.19 (s, 3H), 2.00 (m, 2H), 1.33 (t, /= 7.1 Hz, 3H).

Intermediate 43

r8-(2-Chloro-4.6-dimethyl-phenyl)-2-trifluoromethyI-5.6.7,8-tetrahvdro- imidazo[l,2-a1pyrimidin-3-vπ-methanol, scheme 7: (II) To a solution of the ester (3.43 g, 8.54 mmol) in anhydrous tetrahydrofuran (100 mL) at 0°C under argon was added dropwise a solution of Lithium aluminum hydride (1 M in hexanes, 86 mL). The reaction mixture was stirred for an hour and an aqueous solution of Rochelle salt was added dropwise to quench excess of LAH. The reaction mixture was extracted with ethyl acetate (3x100 mL). The combined organic layer was washed with water (2x), brine and dried (MgSO ). Purification by silica gel column chromatography, using hexanes, ethyl acetate (90:10 to 60:40) afforded product (2.12 g, 5.89 mmol, 69%) as off white solid. LC/MS: t_R= 1.5 min. [M+H]

360. 1H NMR (CDC1₃) δ: 7.10 (s, IH), 6.97 (s, IH), 4.04 (m, 2H), 3.65 (m, 2H), 3.42

(m, 2H), 2.32 ( , 2H), 2.28 (s, 3H), 2.19 (s, 3H).

2-EthyI-8-(2,4,6-trimethyI-phenyl)-5,6,7,8-tetrahydro-imidazori,2-a]pyrimidine- 3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 7: (LL)

A solution of 0.15 g of N-cyclopropylmethyl, N-propyl amine (1.3 mmol) in toluene (5 mL) was treated with 0.47 mL of 2 M trimethylaluminum in hexanes (0.94 mmol). After lh anhydrous toluene solution (2 mL) of the appropriate ethyl ester (59 mg, 0.17 mmol) was added. Refluxed for 4h. Allowed to cool to ambient temperature, diluted with 25 mL dichloromethane and washed with IM NaOH (8 mL), and water (8 mL). Organic layer was evaporated and the residue in 2 mL dimethylformamide was purified by prep HPLC using a 20 min linear gradient of 30-100 % B in A in a 25 min run. Fractions containing the required compound were combined to give

llmg of the amide. LC/MS: t_R = 1.4 min., [M+H] = 409. 1H NMR (CD₃OD) δ 7.10

(2 H, s), 4.20 - 3.20 (8H, 4 x m), 2.47 (2 H, m), 2.38 (2H, m), 2.33 (3 H, s), 2.23 (6 H, s), 1.80 - 1.57 (2 H, m), 1.22 - 0.20 (11 H, 4 x m). Fractions containing unchanged ethyl ester were combined to recover the starting ethyl ester (43 mg) as trifluoroacetate salt.

2-Trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazon,2 alpyrimidine-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 7:

( L)

The corresponding ethyl ester was subjected to Weinreb amidation using standard protocols. The amide obtained was purified by Preparative HPLC with a 15 min linear gradient of B in A in a 20 min run. Combined fractions were evaporated in vacuo to give the required product. LC/MS: t_R = 1.8 min., [M+H] = 449, 1HNMR

(CD₃OD) δ 7.03 (2 H, s), 4.04 - 3.97 (2H, 2 x m), 3.64 (2 H, t, Λi_c = 5.6 Hz), 3.62 -

3.02 (4 H, 4 x m), 2.47 - 2.32 (2 H, m), 2.31 (3 H, s), 2.21 (3 H, s), 2.20 (3H, s), 1.81 - 1.07 (3 H, 3 x m), 1.06 - 0.82 (3 H, 2 x m), 0.70 - 0.02 (4 H, 3 x m).

Intermediate 44

2-Methyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazon,2- a]pyrimidine-3-carboxyIic acid pentafluorophenyl ester, scheme 7: (HH)

The corresponding ethyl ester (0.17 mg, 0.52 mmol) and LiOH-H₂O (110 mg) in

dimethoxyethane:water (1:1, 113 mL) was heated to 55°C for 24 h.

Dimethoxyethane and water were evaporated. The residue in 3 mL dimethyl formamide was treated with pentafluorophenyl trifluoroacetate (2.5 mL) and stirred for 2 h. Volatiles were evaporated and the residue was purified by silica gel column chromatography with methylene chloride and 2-propanol: methylene chloride (3:47). Fractions containing the required activated pentafluorophenyl ester were combined to give 0.15 g, 32 % yield). LC/MS: t_R = 1.5 min., [M+H] = 466.

General Procedure for amide formation preparation of Example 56-58 from Intermediate 44: The pentafluorphenyl ester (15 mg, 0.036 mmol) in 1 mL dimethylformamide was stirred with 0.18 mmol of appropriate amine and 0.18 - 0.36

mmol Cs₂CO₃ at 70°Cfor 18 h. The mixture was diluted with water (0.8 mL) and

trifluoroacetic acid (0.2 mL). The resulting solution was purified by preparative HPLC using a 20 min linear gradient with 30-100 % B in A as eluent in a 25 min run. Fractions containing the required product were combined and evaporated to give the appropriate amide in 20-50 % yield. Example 56

2-MethyI-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazon,2- alpyrimidine-3-carboxylic acid phenethyl-propyl-amide, scheme 7: (LL) Prepared as described for the example above. LC/MS: t^ = 1.3 min., [M+H] = 445,

1H NMR (CD₃OD) δ 7.31 - 7.16 (5 H, m), 7.09 (2 H, s), 4.31 - 2.72 (12 H, 7 x m),

2.32 (3 H, s), 2.20 (6 H, s), 2.05 - 1.43 (5 H, m), 1.28 - 0.77 (3 H, 2 x m).

2-Methyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazori,2- a]pyrimidine-3-carboxyIic acid cyclobutylmethyl-propyl-amide, scheme 7: (LL)

LC/MS: t_R = 1.3 min., [M+H] = 409, 1H NMR (CD₃OD) δ 7.10 (2 H, s), 4.43 - 3.79

(2 H, m), 3.70 (2 H, t, Λi_c = 5.5 Hz), 3.62 - 3.10 (4 H, m), 2.91 - 2.53 (1 H, m), 2.38 - 2.36 (2 H, m), 2.33 (3 H, s), 2.22 (6 H, s), 2.10 - 1.22 (11 H, 4 x m), 1.16 - 0.79 (3 H, m).

2-Methyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahvdro-imidazo[l,2- alpyrimidine-3-carboxylic acid bis-cyclopropylmethyl-amide, scheme 7: (LL)

LC/MS: t_R = 1.4 min., [M+H] = 409, 1H NMR (CD₃OD) δ 7.10 (2 H, s), 4.15 - 3.95

(2 H, m), 3.70 (2 H, t, Λic = 5.5 Hz), 3.68 - 3.36 (4 H, m), 2.39 - 2.36 (2 H, m), 2.33 (3 H, s), 2.23 (6 H, s), 2.09 (3 H, s), 1.25 - 1.05 (4 H, m), 0.41 - 0.05 (4 H, m).

Intermediate 39 was used to prepare Examples 59-95 and 331.

Example 59

Cyclopropylmethyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7 ,8-tetrahydro-imidazori,2-a1pyrimidin-3-ylmethyn-amine, scheme 7: (KK) Intermediate 39 was dissolved in benzene (50 mL)- and treated with with thionyl chloride (5 mL). The solution was heated at reflux for 2h. The volatiles were evaporated. The residue was evaporated twice with heptane (50 mL). The resulting gum was dissolved in acetonitrile (30 mL) and treated with excess N- cyclopropylmethyl, N-propyl-amine (1 mL). After lh LC-MS indicated clean conversion to the required dialkylaminomethyl derivative. Acetonitrile was evaporated and the residue was purified by C18 column chromatography with a step gradient elution using 20-60 % methanol in water containing 0.1 % trifluoroacetic acid. Fractions containing the required product were combined and evaporated in vacuo to give the required amine (0.17g, 51 % overall yield from the cyclization

product). LC/MS: t_R = 1.3 min., [M+H] = 435, 1H NMR (CD₃OD) δ 6.98 (2 H, s),

4.56 (2H, s), 4.16 (2 H, t, Λi_c = 5.8 Hz), 3.60 (2 H, t, Λi_c = 5.5 Hz), 3.23 - 3.18 (4 H, 2 x m), 2.36 (2 H, m), 2.29 (3 H, s), 2.15 (6 H, s), 1.81 - 1.76 (2 H, m), 1.28 -1.21 (1 H, m), 1.02 (3 H, t, Λi_c = 7.3 Hz), 0.86 - 0.82 (2 H, m), 0.51 - 0.47 (2 H, m).

Example 60

3-(3,6-Dihydro-2H-pyridin-l-ylmethyl)-2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-5,6,7,8-tetrahvdro-imidazori,2-a1pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.3 min., MS: [M+H] = 405. Example 61

3-Thiomorpholin-4-ylmethyl-2-trifluoromethyI-8-(2,4,6-trimethyl-phenyl)- 5,6,7,8- tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R = 1.5 min., MS: [M+H]

425.

Example 62

3-Piperidin-l-ylmethyl-2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7.8- tetrahydro-imidazo[l,2-a]pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1-5 min., MS: [M+H] 407. Example 63

3-(2-Methyl-piperidin-l-ylmethyl)-2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min., MS: [M+H] = 421.

Example 64

3-(4-Methyl-piperidin-l-ylmethyl)-2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7 ,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.5 min., MS: [M+H] = 421. Example 65

Benzyl-methyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro- imidazo[l,2-a1pyrimidin-3-yImethyl]-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.5 min., MS: [M+H] = 443.

Example 66

Methyl-phenethyl-r2-trifluoromethyl-8-(2,4,6-trimethvI-phenyl)-5,6,7,8- tetrahydro-imidazori,2-a]pyrimidin-3-ylmethvπ-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.5 min., MS: [M+H] = 457. Example 67

Diallyl-r2-trifluoromethyl-8-(2.4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro- imidazo[l,2-a]pyrimidin-3-ylmethvn-amine, scheme 7: (KK) Prepared as described for the example above. LC MS: to = 1.4 min., MS: [M+H] 419.

Example 68

Dipropyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min., MS: [M+H] 423.

Example 69

Butyl-methyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahvdro- imidazo[l,2-a]pyrimidin-3-ylmethyl1-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min., MS: [M+H] = 409.

Example 70

Butyl-ethyl-[2-trifluoromethyI-8-(2,4,6-trimethyI-phenyl)-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethvn-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.4 min., MS: [M+H] = 423.

Example 71

Ethyl-(2-methyI-allyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5.6.7.8- tetrahvdro-imidazori,2-alpyrimidin-3-yImethyl1-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.6 min., MS: [M+H] = 421.

Example 72

3-(3-Phenyl-pyrrolidin-l-ylmethyl)-2-trifluoromethyI-8-(2,4,6-trimethyl- phenyl)-5,6,7,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = L8 min., MS: [M+H] 469.

Example 73

Cvclopropylmethyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4.6-trimethyl- phenyl)-5,6,7,8-tetrahydro-imidazo[l,2-a]pyrimidin-3-ylmethyll-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] = 475.

Example 74

Cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)-[2trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-5,6,7,8-tetrahvdro-imidazori,2-a1pyrimidin-3-ylmethyn- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min., MS: [M+H] = 525.

Example 75

Cyclopropylmethyl-ethyl-[2-trifluoromethyI-8-(2,4,6-trimethyl-phenyl)-5,6,7,8- tetrahydro-imidazori,2-a1pyrimidin-3-yImethvn-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.3 min., MS: [M+H] = 421.

Example 76

Cvclobutylmethyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-5,6,7,8-tetrahydro-imidazo[l,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK)

Prepared as described for the example above. LC MS: to = 1.9 min., MS: [M+H] = 489.

Example 77

Cvclobutylmethyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyI-phenyl)-5,6,7,8- tetrahydro-imidazori,2-alpyrimidin-3-ylmethyI]-amine. scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.7 min., MS: [M+H] 449.

Example 78

Propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro- imidazori,2-alpyrimidin-3-ylmethyI1-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] = 477.

Example 79

Propyl-(2,2.2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4.6-trimethyl-phenyl>- 5,6,7,8-tetrahvdro-imidazo[l,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK) -Ill-

Prepared as described for the example above. LC/MS: to = L9 min., MS: [M+H] = 463.

Example 80

(2,2,3,3,3-Pentafluoro-propyl)-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-5,6,7,8-tetrahydro-imidazori,2-a]pyrimidin-3-ylmethyl1-amine, scheme

7: (KK)

Prepared as described for the example above. LC/MS: to = 2.0 min., MS: [M+H] = 513.

Phenethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro- imidazo[l,2-a]pyrimidin-3-ylmethyIl-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R = 2.0 min., MS: [M+H] = 539.

Example 82

Phenethyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7,8-tetrahydro-imidazon,2-a1pyrimidin-3-ylmethvI1-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.9 min., MS: [M+H] =

525.

Example 83

Phenethyl-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8- tetrahydro-imidazori,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] 485. Example 84

Ethyl-phenethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8- tetrahvdro-imidazo[l,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.7 min., MS: [M+H] 471.

Example 85

Benzyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4.6-trimethyl-phenyl)- 5,6,7,8-tetrahvdro-imidazori,2-a1pyrimidin-3-ylmethyll-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] = 511.

Benzyl-r2-trifluoromethyl-8-(2,4,6-trimethyI-phenyl)-5,6,7,8-tetrahydro- imidazo[l,2-a1pyrimidin-3-ylmethvn-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = L8 min., MS: [M+H] = 525.

Example 87

(2-Cyclopropyl-ethyl)-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7,8-tetrahydro-imidazori,2-alpyrimidin-3-ylmethyn-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.7 min., MS: [M+H] = 449. Example 88

(2-Cyclopropyl-ethyl)-ethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 5,6,7,8-tetrahydro-imidazo[l,2-a]pyrimidin-3-ylmethyl]-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1-5 min., MS: [M+H] = 435.

(2-Cvclopropyl-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5.6.7.8- tetrahydro-imidazori,2-alpyrimidin-3-ylmethvn-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 2.0 min., MS: [M+H] = 503. Example 90

(2-Cvclopropyl-ethyl)-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazori,2-a1pyrimidin-3-ylmethyl]- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] 489.

Example 91

(4-Fluoro-benzyI)-r2-trifluoromethvI-8-(2,4,6-trimethyl-phenyl)-5.6.7.8- tetrahydro-imidazori,2-a]pyrimidin-3-yImethyl1-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min., MS: [M+H] = 543. Example 92

(4-Fluoro-benzyl)-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8- tetrahydro-imidazo[l,2-a]pyrimidin-3-ylmethvn-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.7 min., MS: [M+H] = 489.

Example 93

(4-Chloro-benzyl)-r2-trifluoromethyl-8-(2.4.6-trimethyl-phenyl)-5,6,7,8- tetrahydro-imidazori,2-a1pyrimidin-3-ylmethyl]-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min., MS: [M+H] = 559. Example 94

(4-Chloro-benzyl)-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8- tetrahydro-imidazori,2-a1pyrimidin-3-ylmethyl1-amine, scheme 7: (KK)

Prepared as described for the example above. LC MS: to = 1.8 min., MS: [M+H] = 505.

Example 95

Allyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahvdro- imidazon.2-alpyrimidin-3-ylmethyn-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.5 min., MS: [M+H] = 421.

Intermediate 43 was used to prepare Examples 96-138. Example 96

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazo[l,2-a1pyrimidin-3-ylmethyl]-cyclopropylmethyl-propyl-amine, scheme 7: (KK)

To a solution of the appropriate alcohol (0.092 mg, 0.25 mmol) in benzene (20 mL)

was added thionyl chloride (0.15 g, 1.28 mmol) at 0°C, under argon. The reaction

mixture was stirred for an hour the solvent was removed on a rotary evaporator. Traces of thionyl chloride were removed by co-evaporating with dichloromethane 3 times. The residue was dissolved in dichloromethane (50 mL) and to that solution was added the N-propyl-cyclopropylmethylamine (0.058 g, 0.512 mmol) and diisopropylethyl amine (0.099 g, 0.768 mmol) at rt. The reaction mixture was stirred overnight. Solvent was concentrated, the residue dissolved in methanol (2 mL) and purification carried out by reverse phase preparative HPLC using water, methanol, , trifluoroacetic acid to obtain the product (0.084 g, 0.15 mmol, 70%) as colorless oil.

LC/MS: to= 1-4 min. [M+H] 455. 1H NMR (CD₃OD) δ: 7.20 (s, IH), 7.11 (s, IH),

4.58 (m, 2H), 4.19 (m, 2H), 3.68 (m, IH), 3.59 (m, IH), 3.23 (m, 4H), 2.39 (m, 2H), 2.33 (s, 3H), 2.23 (s, 3H), 1.79 ( , 2H), 1.22 ( , IH), 1.01 (t, J = 7.3 Hz, 3H0, 0.83 (m, 2H), 0.50 (m, 2H). Example 97

8-(2-Chloro-4,6-dimethyl-phenyl)-3-morphoIin-4-ylmethyl-2-trifluoromethyl- 5,6,7 ,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.3 min. [M+H] 429.

Example 98

8-(2-Chloro-4,6-dimethyl-phenyl)-3-thiomorpholin-4-ylmethyl-2- trifluoromethyl-5,6,7,8-tetrahydro-imidazori,2-a1pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: t_R= 1.3 min. [M+H] 445.

Example 99

8-(2-Chloro-4,6-dimethyl-phenyl)-3-piperidin-l-ylmethyl-2-trifluoromethyl- 5,6,7,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R= 1.4 min. [M+H] 427.

Example 100

8-(2-Chloro-4,6-dimethyl-phenyl)-3-(2-methyl-piperidin-l-ylmethyl)-2- trifluoromethyI-5,6,7,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: t_R= 1.4 min. [M+H] 441.

Example 101

8-(2-ChIoro-4,6-dimethyl-phenyl)-3-(3-methyl-piperidin-l-ylmethyl)-2- trifluoromethyl-5,6,7,8-tetrahvdro-imidazon,2-a1pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.4 min. [M+H] 441. Example 102

8-(2-ChIoro-4,6-dimethyl-phenyI)-3-(4-methyl-piperidin-l-ylmethyI)-2- trifluoromethyl-5,^,7,8-tetrahydro-imidazori,2-a]pyrimidine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.4 min. [M+HJ 441.

Example 103

Diallyl-r8-(2-chIoro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazon,2-a]pyrimidin-3-ylmethyn-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min. [M+H] 439.

Example 104

Butyl-[8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazo[l,2-a]pyrimidin-3-ylmethvn-methyl-amine, scheme 7: (KK) Prepared as described for the example above. LC MS: t_R= 1.4 min. [M+H] 429.

Example 105

Benzyl-butyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyI-5,6,7,8- tetrahydro-imidazori,2-a]pyrimidin-3-ylmethyll-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.6 min. [M+H] 506.

Example 106

[8-(2-ChIoro-4,6-dimethyl-phenyI)-2-trifluoromethyl-5,6.7,8-tetrahvdro- imidazo[l,2-a1pyrimidin-3-ylmethyn-ethyl-(2-methyl-alIyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to= 1.4 min. [M+H] 441. Example 107

Benzyl-[8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethvn-methyI-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.5 min. [M+H] 463.

Butyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazori,2-a]pyrimidin-3-yImethvn-ethyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min. [M+H] 443.

Example 109

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyl]-dipropyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min. [M+HJ 443.

Example 110

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazo[l,2-a]pyrimidin-3-ylmethvn-(2-methoxy-ethyI)-propyl-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R= 1.4 min. [M+H] 459.

r8-(2-Chloro-4.6-dimethyI-phenyl)-2-trifluoromethyl-5.6,7,8-tetrahvdro- imidazori,2-a1pyrimidin-3-yImethyl]-cyclobutylmethyl-propyl-amine, scheme 7:

(KK)

Prepared as described for the example above. LC MS: to = 1.5 min. [M+H] 470. Example 112

[8-(2-ChIoro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-ylmethyll-cyclobutylmethyl-(2,2,2-trifluoro-ethyl)- amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.9 min. [M+H] 509.

Example 113

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5.6,7.8-tetrahydro- imidazo [1 ,2-a]pyrimidin-3-yImethyl1 -cyclopropylmethyl-ethyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.4 min. [M+H] 441.

Example 114

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-ylmethyl]-propyl-(2,2,2-trifluoro-ethyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1-8 min. [M+H] 483.

Example 115

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyI-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-yImethvn-cyclopropyImethyl-(2,2,3,3,3-pentafluoro- propyD-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min. [M+H] 545. Example 116

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyn-propyl-(3,3,3-trifluoro-propyI)-amine, scheme 7: (KK)

Prepared as described for the example above. LC MS: to = 1.7 min. [M+H] 497.

Example 117

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazori,2-a]pyrimidin-3-ylmethyll-(2,2,3,3,3-pentafluoro-propyl)-propyl- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min. [M+ffJ 533. Example 118

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-ylmethyl1-phenethyI-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min. [M+H] 560.

Example 119

r8-(2-ChIoro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7.8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyl]-phenethyl-(2,2,2-trifluoro-ethyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.9 min. [M+H] 545. Example 120

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyn-ethyl-phenethyl-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to= L6 min. [M+H] 491.

Example 121

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethvn-phenethyl-propyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to= 1.6 min. [M+H] 505.

Example 122

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazo[l,2-a]pyrimidin-3-ylmethyll-(2-cyclopropyl-ethyl)-(3,3,3-trifluoro- propyl)-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min. [M+H] 523.

r8-(2-ChIoro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5.6.7.8-tetrahvdro- imidazori,2-a]pyrimidin-3-ylmethyl1-(2-cyclopropyl-ethyl)-ethyl-amine, scheme

7: (KK)

Prepared as described for the example above. LC/MS: t_R= 1.5 min. [M+H] 455. Example 124

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyl]-(2-cyclopropyl-ethyl)-propyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.5 min. [M+H] 469.

Example 125

Benzyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyn-(3,3,3-trifluoro-propyl)-amine, scheme 7:

(KK)

Prepared as described for the example above. LC/MS: to = 1.8 min. [M+H] 545.

Example 126

r8-(2-Chloro-4,6-dimethyl-phenyl)-2>trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-ylmethyl]-(2-cvclopropyl-ethyl)-(2,2,2-trifluoro- ethyl)-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1-8 min. [M+H] 509.

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyI-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-yImethyl]-(4-fluoro-benzyl)-(3,3,3-trifluoro-propyl)- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.8 min. [M+H] 563.

Example 128

(4-Chloro-benzyl)-r8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8- tetrahvdro-imidazori,2-a1pyrimidin-3-ylmethyll-(3,3,3-trifluoro-propyl)-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R= 1.8 min. [M+H] 580.

Example 129

(4-ChIoro-benzyl)-r8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8- tetrahvdro-imidazori,2-a]pyrimidin-3-ylmethyl1-propyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.7 min. [M+HJ 526.

Example 130

Benzyl-r8-(2-chloro-4,6-dimethvI-phenyI)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazo[l,2-a1pyrimidin-3-ylmethyn-propyI-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: t_R = 1.5 min. [M+H] 491.

Example 131

AIlyl-[8-(2-chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a1pyrimidin-3-ylmethyl]-propyl-amine, scheme 7: (KK) Prepared as described for the example above. LC/MS: to = 1.4 min. [M+HJ 441.

Example 132

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazori,2-a1pyrimidin-3-ylmethyl1-(4-fluoro-benzyl)-propyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.6 min. [M+H] 509.

Example 133

r8-(2-Chloro-4,6-dimethyI-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazori,2-a1pyrimidin-3-ylmethyl]-(3-fluoro-benzyl)-(3,3,3-trifluoro-propyl)- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: t = 1.8 min. [M+H] 563.

Example 134

r8-(2-ChIoro-4,6-dimethyl-phenyl)-2-trifluoromethyI-5,6,7,8-tetrahydro- imidazoπ,2-a]pyrimidin-3-ylmethyl1-(3-fluoro-benzyI)-propyl-amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: to = 1.6 min. [M+H] 509.

Example 135

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahvdro- imidazori,2-a1pyrimidin-3-ylmethyl]-cyclopropylmethyl-(2,2,2-trifluoro ethyl)- amine, scheme 7: (KK)

Prepared as described for the example above. LC/MS: t_R= 1.8 min. [M+H] 495.

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5.6.7.8-tetrahydro- imidazo[l,2-a]pyrimidin-3-yImethyl]-(4-nitro-benzyl)-propyl-amine, scheme 7:

(KK) Prepared as described for the example above. LC/MS: to = 1.7 min. [M+H] 536.

Example 137

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-trifluoromethyl-5,6,7,8-tetrahydro- imidazori,2-a]pyrimidin-3-ylmethyn-cycIobutylmethyl-ethyl-amine, scheme 7:

(KK)

Prepared as described for the example above. LC/MS: to = 1.4 min. [M+H] 455.

Example 138

3-(2-Benzyl-pyrrolidin-l-yImethyl)-8-(2-chloro-4,6-dimethvI-phenyl)-2- trifluoromethyl-5,6,7,8-tetrahydro-imidazon,2-a1pyrimidine. scheme 7: (KK)

LC/MS: to= 1-5 min. [M+H] 503.

The following Intermediates 45-94 may be used to synthesize Examples 139-282. Intermediate 45

(4-Fluoro-2-nitro-phenyl)-(2,4,6-trimethyl-phenyl)-amine¹, scheme 1: (B)

A mixture of 2,4,6-trimethlaniline (42.1 mL, 300 mmol), 2,5-difluoro-nitrobenzene (16.3 mL, 150 mmol) and anhydrous potassium fluoride (10.5 g, 180 mmol) was

heated and stirred at 180°C for 60 h. After cooling, the mixture was partitioned

between dichloromethane (170 mL) and water (150 mL). The aqueous layer was extracted with dichloromethane (60 mL). The combined organic layers were washed with water and brine. Solvents were removed in vacuo and the residue purified by silica gel chromatography eluting with 40% dichloromethane/hexanes to afford the

title compound as a red solid (36.92 g, 100% yield). 1H NMR (CDC1₃, 300 MHz) δ

9.00 (s, IH), 7.93 (dd, J = 9.1, 3.0 Hz, IH), 7.12 - 7.05 (m, IH), 6.99 (s, 2H), 6.37

(dd, J = 9.4, 4.7 Hz, IH), 2.33 (s, 3H), 2.14 (s, 6H); ¹³C NMR (CDC1₃, 75 MHz) δ

154.6, 151.4, 141.8, 137.6, 136.3, 132.6, 129.6, 124.9 (d, J = 23.8 Hz), 116.5 (d, J = 7.0 Hz), 111.75 (d, J = 26.2 Hz).

Intermediate 46

(2-Nitro-phenyI)-(2,4,6-trimethyl-phenyl)-amine:³, scheme 1: (B) Prepared as described for the example above. Chromatography using dichloromethane/hexanes (30%) as eluent and recrystallization from anhydrous ethanol afforded the title compound as orange needle crystals (15.4 g, 40% yield). 1H

NMR (CDCI₃, 300 MHz) δ 9.13 (br s, IH), 8.23 (d, J = 8.4 Hz, IH), 7.28 (t, J = 7.2

Hz, IH), 7.00 (s, 2H), 6.70 (t, J = 7.2 Hz, IH), 6.39 (d, J = 8.4 Hz, IH), 2.35 (s, 3H), 2.16 (s, 6H).

Intermediate 47

(2-Bromo-4-isopropyl-phenyl)-(2-nitro-phenyl)-amine, scheme 1: (B)

Prepared as described for the example above. Chromatography using dichloromethane/hexanes (20%) as eluent and vacuum distillation to remove unreacted 2-bromo-4-t^",rø-propylaniline afforded the title compound as a red solid (12

g, 24% yield). 1H NMR (CDCI₃, 300 MHz) δ 9.41 (br s, IH), 8.21 (dd, J = 8.6, 1.6

Hz, IH), 7.54 (d, J = 2.0 Hz, IH), 7.38 - 7.33 (m, 2H), 7.20 (dd, J = 8.1, 2.0 Hz, IH), 7.08 (dd, J = 8.6, 1.0 Hz, IH), 6.81 (t, J = 7.0 Hz, IH), 2.92 (septet, J = 7.0 Hz, IH), 1.27 (d, J = 6.9 Hz, 6H).

Intermediate 48

(2,4-DichIoro-phenyI)-(2-nitro-phenyI)-amine, scheme 1: (B) Prepared as described for the example above. Chromatography using dichloromethane/hexanes (10% and 20%) as eluent and recrystallization from 95% ethanol afforded the title compound as red needle crystals (8.5 g, 20% yield). 1H

NMR (CDC1₃, 400 MHz) δ 9.39 (s, IH), 8.22 (dd, J = 8.5, 1.5 Hz, IH), 7.51 (d, J =

2.3 Hz, IH), 7.45 - 7.38 (m, 2H), 7.27 (dd, J = 8.6, 2.3 Hz, IH), 7.13 (dd, J = 8.6, 1.0

Hz, IH), 6.88 (td, J = 7.8, 1.2 Hz, IH); ¹³C NMR (CDC1₃, 100 MHz) δ 141.0, 135.7,

135.1, 134.6, 130.5, 130.3, 129.3, 127.9, 126.8, 124.8, 118.9, 116.2.

Intermediate 49

(3-Nitro-pyridin-2-yl)-(2,4,6-trimethyl-phenyl)-amine, scheme 1: (B)

A mixture of 2-chloro-3-nitro-pyridine (24.05 g, 152 mmol), 2,4,6-trimethylaniline

(60 ml, 427 mmol), and Cs₂CO₃ (59.4 g, 182.4 mmol) was heated at 100 °C for 24 h.

Flash chromatography using 1) methylene chloride /Hexanes (1:4) and 2) methylene chloride, followed by recrystallization from 95% ethanol. The title compound was obtained as an orange-yellow crystals (17.0 g, 44% yield). ^JH NMR (CDC1₃, 5 MHz)

δ 9.38 (s, IH), 8.51 (d, J = 5.8 Hz, IH), 8.38 (s, IH), 7.00 (s, 2H), 6.73 (s, IH), 2.34

(s, 3H), 2.18(s, 6H); ¹³C NMR (CDC1₃, 100 MHz) δ 156.2, 152.1, 137.2, 135.7,

135.4, 132.3, 129.1, 128.3, 112.8, 21.1, 18.5. Intermediate 50

(2-Chloro-4,6-dimethylphenyl)-(3-nitro-pyridin-2-yl)-amine, scheme 1: (B)

A mixture of 2-chloro-3-nitro-pyridine (55.8 g, 352 mmol), 2-chloro-4,6-

trimethylaniline (110 g, 704 mmol), and KF (28.6 g, 493 mmol) was heated at 190°C

for 40 h. After cooling to room temperature, the mixture was extracted with methylene chloride and IN NaOH. The combined organic layers were washed with water and brine, then dried over MgSO . Solvents were removed in vacuo, and the residue was subjected to vacuum distillation to remove unreacted 2-chloro-4,6- trimethylaniline. The resulting brownish solid was subjected to flash chromatography using 1) methylene chloride /hexanes (1:1) and 2) methylene chloride, followed by recrystallization from 95% ethanol. The title compound was

obtained as yellow crystals (9.8 g, 10% yield). 1H NMR (CDC1₃, 500 MHz) δ 9.39 (br s, IH), 8.51 (dd, J = 8.3, 1.8 Hz, IH), 8.37 (dd, J = 4.5, 1.7 Hz, IH), 7.18 (s, IH), 7.04 (s, IH), 6.78 (dd, J = 8.3, 4.5 Hz, IH), 2.33 (s, 3H), 2.21 (s, 3H).

Intermediate 51

4-Fluoro-N¹-(2,4,6-trimethyl-phenyl)-benzene-l,2-diamine. scheme 1: (C) Palladium on carbon (10%) (0.54 g) was added to a solution of (4-fluoro-2-nitro- phenyl)-(2,4,6-trimethyl-phenyl)-amine (5.32 g, 19.4 mmol) in ethyl acetate (40 mL) under nitrogen at room temperature in a 500 mL round-bottomed flask. The flask was evacuated under high vacuum (<2 mm Hg) and purged with hydrogen six times at room temperature, then it was attached to a balloon filled with hydrogen. After the reaction mixture was stirred at room temperature for 4.0 h under 1 atmosphere of hydrogen, the balloon was removed and a stream of nitrogen was bubbled through the reaction mixture for 10 min. The reaction mixture was filtered through a pad of celite and solvents were removed in vacuo to afford the title compound as a red solid (4.74 g, 100% yield). The purity of this compound was determined to be 98% by

LC/MS. 1H NMR (CDCI3, 300 MHz) δ 6.93 (s, 2H), 6.52 (dd, J = 9.8, 2.7 Hz, IH), 6.32 (td, J = 8.6, 2.7 HZ, IH), 6.22 (dd, J = 8.7, 5.7 Hz, IH), 2.32 (s, 3H), 2.12 (s,

6H); ¹³C NMR (CDC1₃, 75 MHz) δ 159.8, 156.7, 138.2 (d, J = 10.5 Hz), 137.6, 133.5,

132.3, 129.5, 117.3 (d, J = 9.5 Hz), 105.1 (d, J = 22 Hz), 102.9 (d, J = 25.5 Hz),20.8, 18.0; Mass spec: 245.14 (MH^4")

Intermediate 52

N- (2,4,6-Trimethyl-phenvD-benzene- 1 ,2-diamine, scheme 1: (C) Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 6.92 (s,

2H), 6.88 (d, J = 7.5 Hz, IH), 6.78 - 6.70 (m, 2H), 6.25 (d, J = 7.2 Hz, IH), 4.95 (br s, 2H), 2.31 (s, 3H), 2.13 (s, 6H); Mass spec: 227.15 (MH^1")

Intermediate 53

N-(2,4-Dichloro-phenyl)-benzene-l,2-diamine, scheme 1: (C)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.31 -

7.00 (m, 4H), 6.89 - 6.79 (m, 2H), 6.52 (d, J = 8.8 Hz, IH), 5.74 (s, IH), 4.27 (br s, 2H); Mass spec: 253.12 (MH^1")

Intermediate 54

N²-(2,4,6-Trimethyl-phenyl)-pyridine-2,3-diamine, scheme 1: (C) Prepared as described for the example above. Mass spec: 228.16 (MH ^")

Intermediate 55

N-(2-Bromo-4-isopropyl-phenyl)-benzene-l,2-diamine². scheme 1: (C) To a solution of (2-bromo-4-isopropyl-phenyl)-(2-nitro-phenyl)-amine (8.2 g, 24.5 mmol) in tetrahydrofuran (35 mL) and water (35 mL) at room temperature, was added NΗ₄OH (33.6 mL) and Na₂S₂O₄ (21.3 g, 122.5 mmol. After stilting at room temperature for 5 h, water (70 mL) was added and the mixture was extracted with ethyl acetate (175 mL). After separation, the aqueous layer was saturated with NaCl,

and extracted with ethyl acetate (3 x 60 mL). The combined organic layers were

washed with sat. NaHCO₃, water, brine, and dried over Na₂SO₄. Solvents were removed in vacuo to afford the title compound a red viscous liquid (5.3 g, 71% yeld). The purity of this compound was determined to be 95% by LC/MS and it was used for the next step without further purification. Mass spec: 307.08 (MH^4").

Intermediate 56

N²-(2-Chloro-4,6-dimethyl-phenyl)-pyridine-2,3-diamine, scheme 1: (C)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.71

(dd, J = 5.0, 1.5 Hz, IH), 7.11 (s, IH), 6.97 (dd, J = 7.5, 1.6 Hz, IH), 6.96 (s, IH), 6.67 (dd, J = 7.5, 5.0 Hz, IH), 5.89 (br s, IH), 3.53 (br s, 2H), 2.29 (s, 3H), 2.13 (s, 3H); Mass spec: 228.16 (MH^4")

Intermediate 57 5-Fluoro-l-(2,4,6-trimethyl-phenyl)-lH-benzoimidazol-2-ylamine:³, scheme 1:

(D)

A solution of cyanogen bromide (2.67 g, 25.2 mmol) in anhydrous ethanol (10 mL)

was added at 0°C to a solution of 4-fluoro-N¹-(2,4,6-trimethyl-phenyl)-benzene-l,2-

diamine (4.74 g, 19.4 mmol) in anhydrous ethanol (20 mL) under nitrogen. The reaction mixture was warmed up to room temperature for 10 min, then was heated at

155°C for 40 min with a flow of nitrogen to remove ethanol. Upon cooling to room

temperature, the resulting solids were transferred to a separatory funnel via

dichloromethane (70 mL), and washed sequentially with 1 Ν sodium hydroxide (2 x

35 mL), water and brine. The organic layer was dried over anhydrous sodium sulfate and solvents were removed in vacuo to afford the title compound as a red solid (5.11 g, 98% yield). The purity of this compound was determined to be 95% by LC/MS.

1HΝMR (CDCI₃, 300 MHz) δ 7.12 (dd, J = 9.7, 2.4 Hz, IH), 7.06 (s, 2H), 6.69 (td, J

= 9.1, 2.4 Hz, IH), 6.56 (dd, J = 8.5, 4.7 Hz, IH), 2.38 (s, 3H), 1.98 (s, 6H); ¹³C

NMR (CDCI3, 75 MHz) δ 161.0, 157.9, 154.2, 143.3, 139.9, 137.4, 129.8, 128.8,

107.8 (d, J = 10.2 Hz), 106.9 (d, J = 25.3 Hz), 103.1 (d, J = 25.2 Hz)21.1, 17.5; Mass spec: 270.17 (Mϊ ).

Intermediate 58 l-(2,4,6-Trimethyl-phenyl)-lH-benzoimidazol-2-ylamine, scheme 1: (D)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.46 (d,

J = 8.1 Hz, IH), 7.16 (td, J = 7.6, 1.2 Hz, IH), 7.06 (s, 2H), 7.01 (td, J = 7.2, 0.6 Hz, IH), 6.71 (dd, J = 7.8, 0.6 Hz, IH), 2.38 (s, 3H), 1.98 (s, 6H); Mass spec: 252.09 (MH^4")

l-(2,4-Dichloro-phenyl)-l#-benzoimidazol-2-ylamine, scheme 1: (D)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.67 (d, J = 1.5 Hz, IH), 7.49 - 7.41 (m, 2H), 7.23 - 7.16 (m, 2H), 7.04 (t, J = 7.7 Hz, IH), 6.77 (d, J = 7.9 Hz, IH); Mass spec: 278.08 (MH")

Intermediate 60

l-(2-Bromo-4-isopropyI-phenyI)-lH-benzoimidazoI-2-ylamine, scheme 1: (D)

Prepared as described for the example above. Mass spec: 330.08 (MH^1") Intermediate 61

3-(2,4,6-Trimethyl-phenyl)-3H^r-imidazor4,5-b]pyridin-2-ylamine, scheme 1: (D) To a mixture of N²-(2,4,6-Trimethyl-phenyl)-pyridine-2,3-diamine (3.05 g, 13.4

mmol), NaHCO₃ (2.03 g, 24.1 mmol) in ethanol (40 mL) at 0°C, was added a

solution of BrCN (2.55 g, 24.1 mmol) in ethanol (6 mL). The resulting mixture was

stirred at 0°C for 1 h, room temperature for 8 h, and then 80°C for 8 h. Ethanol was

removed in vacuo and the residue was taken up into a separatory funnel with methylene chloride (100 mL). The mixture was washed sequentially with IN NaOH, water and brine, then the organic layer was dried over Na₂SO₄. After removing solvents, a brown solid was obtained. By LC-MS, the solid was a mixture of the desired product and the unreacted starting material in a ratio of 4: 1 in favor of the desired product. Mass spec: 253.17 (MH^4").

Intermediate 62

3-(2-Chloro-4,6-dimethyl-phenyn-3H^r-imidazo[4,5-blpyridin-2-ylamine, scheme 1: (D) Prepared as described for the example above. Mass spec.273.20 (MH^1") Intermediate 63

3-Ethoxycarbonylmethyl-l-(2,4,6-trimethylphenyI)-2-amino-5-fluoro- benimidazolium bromide:⁴, scheme 1: (E)

Ethyl bromoacetate (2.3 mL, 20.9 mmol) was added at room temperature to a solution of 5-fluoro-l-(2,4,6-trimethyl-phenyl)-lH-benzoimidazol-2-ylamine (5.11 g, 19.0 mmol) in acetone (100 mL). The resulting mixture was heated at reflux for 14 h. Upon cooling to room temperature, acetone was removed in vacuo. Solids were

transferred onto a filtering funnel and washed with ether (2x15 mL) to afford the title

compound as a pink solid (7.42 g, 90%). The solids were used for the next step

without further purification. 1H NMR (CDC1₃, 300 MHz) δ 8.44 (s, 2H), 7.11 (s,

2H), 7.11 - 6.96 (m, 2H), 6.78 (dd, J = 8.6, 4.1 Hz, IH), 5.69 (s, 2H), 4.28 (qd, J = 7.1, 1.0 Hz, 2H), 2.38 (s, 3H), 2.02 (s, 6H), 1.32 (tdj = 7.1, 1.2 Hz, 3H); ¹³C NMR

(CDCI₃, 75 MHz) δ 165.8, 162.0, 158.7, 151.1, 142.3, 136.9, 130.7, 126.2, 124.7,

112.4 (d, J = 25.0 Hz), 111.2 (d, J = 9.4 Hz), 98.7 (d, J = 29.2 Hz), 63.0, 46.8, 21.3, 17.4, 14.1. Intermediate 64

3-Ethoχycarbonylmethyl-l-(2,4,6-trimethyIphenyI)-2-aminobenimidazolium bromide, scheme 1: (E)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.21 (s,

2H), 7.37 (dd, J = 7.5, 1.2 Hz, IH), 7.32 - 7.28 (m, 2H), 7.12 (s, 2H), 6.86 (d, J = 7.8 Hz, IH), 5.71 (s, 2H), 4.29 (q, J = 7.2 Hz, 2H), 2.40 (s, 3H), 2.03 (s, 6H), 1.33 (t, J = 7.5 Hz, 3H).

Intermediate 65

3-Ethoxycarbonylmethyl-l-(2,4-dichlorolphenyl)-2-aminobenimidazolium bromide, scheme 1: (E)

Prepared as described for the example above. 1H NMR (CDCI₃, 300 MHz) δ 9.16 (s,

2H), 7.68 (d, J = 1.9 Hz, IH), 7.60 - 7.55 (m, 2H), 7.34 - 7.19 ( , 3H), 6.83 (d, J = 7.8 Hz, IH), 5.55 (s, 2H), 4.26 (q, J = 7.6 Hz, 2H), 1.30 (t, J = 7.8 Hz, 3H).

Intermediate 66

2-Amino-3-(2-bromo-4-isopropyl-phenyl)-l-ethoxycarbonylmethyl-3H- benzoimidazol-1-ium bromide, scheme 1: (E)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.48 (s,

2H), 7.72 (s, IH), 7.47 (s, 2H), 7.39 - 7.24 (m,3H), 6.91 (d, J = 7.8 Hz, IH), 5.66 (s, 2H), 4.30 (q, J = 7.1 Hz, 2H), 3.03 (sept., J = 6.9 Hz, IH), 1.32 (d, J = 6.9 Hz, 6H), 1.30 (t, J = 7.1 Hz, 3H).

Intermediate 67

2-Amino-l-ethoxycarbonylmethyl-3-(2,4,6-trimethyl-phenyl)-3H^r-imidazo[4,5- blpyridin-1-ium bromide, scheme 1: (E)

Prepared as described for the example above. Mass spec: 339.21 (M - HBr + H)^4".

Intermediate 68

2-Amino-3-(2-chloro-4,6-dimethyl-phenyl)-l-ethoxycarbonylmethyl-3H^r- imidazo[4,5-b]pyridin-l-ium bromide, scheme 1: (E) Prepared as described for the example above. Mass spec: 359.20 (M - HBr + H)^4".

Intermediate 69

5-Fluoro-2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cyclopentarα]indene-3-carboxylic acid ethyl ester:⁴, scheme 1: (F)

A mixture of 3-ethoxycarbonylmethyl-l-(2,4,6-trimethylphenyl)-2-amino-5-fluoro- benimidazolium bromide (2.0 g, 4.59 mmol), sodium acetate (0.94 g, 11.4 mmol) and

acetic anhydride (14.0 mL) was heated at 160°C for 20 h. Upon cooling, the mixture was poured into a flask containing ice. While stirring, excess sodium bicarbonate was added to the above mixture in small portions, and the resulting mixture was stirred at room temperature for 6 h. Then, the mixture was extracted with

dichloromethane (2x70 mL). The organic extracts were washed with water and dried

over anhydrous sodium sulfate. Solvents were removed in vacuo and the residue was subjected to chromatography using ethyl acetate/hexanes (1:9) as eluent to afford the

title compound as a white solid (1.33 g, 16% yield). 1H NMR (CDC1₃, 300 MHz) δ

8.39 (d, J = 9.3 Hz, IH), 7.03 (s, 2H), 6.98 (dd, J = 9.0, 2.2 Hz, IH), 6.81 (dd, J = 8.8, 4.5 Hz, IH), 4.47 (q, J = 7.1 Hz, 2H), 2.63 (s, 3H), 2.35 (s, 3H), 1.95 (s, 6H), 1.48 (t,

J = 7.1 Hz, 3H); ¹³C NMR (CDC1₃, 75 MHz) δ 161.1, 159.6, 156.4, 153.1, 149.3,

139.7, 136.9, 129.9 (d, J = 228 Hz), 129.7, 125.8 (d, J = 13.6 Hz), 112.9, 111.1 (d, J = 25.0 Hz), 110.4 (d, J = 9.5 Hz), 103.2 (d, J = 30 Hz), 60.3, 21.1, 17.7, 16.6, 14.7; Mass spec: 380.21 (MH^4").

Intermediate 70

2-Ethyl-5-fluoro-8-(2,4.6-trimethyl-phenyl)-8H-l,3a,8-triaza- cvclopentarαlindene-3-carboxyIic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.38

(dd, J = 9.4, 2.4 Hz, IH), 7.03 (s, 2H), 7.01 - 6.95 (m, IH), 6.80 (dd, J = 8.8, 4.5 Hz, IH), 4.47 (q, J = 7.1 Hz, 2H), 3.01 (q, J = 7.6 Hz, 2H), 2.35 (s, 3H), 1.95 (s, 6H), 1.47

(t, J = 7.1 Hz, 3H), 1.27 (t, J = 7.6 Hz, 3H); ¹³C NMR (CDC1₃, 75 MHz) δ 161.0, 159.6, 159.0, 156.4, 149.7, 139.7, 136.9, 130.0 (d, J = 227 Hz), 129.8, 125.7 (d, J = 14.0 Hz), 112.8, 111.1 (d, J = 24.9 Hz), 110.4 (d, J = 9.6 Hz), 103.3 (d, J = 29.6 Hz), 60.3, 23.7, 21.1, 17.7, 14.6, 14.4; Mass spec: 394.19 (MH ^")

Intermediate 71

2-MethvI-8-(2,4,6-trimethyl-phenyl)-8H^r-l,3a,8-triaza-cycIopentar ]indene-3-

carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.43 -

8.40 (m, IH), 7.12 - 7.06 (m, 2H), 6.85 (s, 2H), 6.73 - 6.70 (m, IH), 4.29 (q, J = 7.2 Hz, 2H), 2.46 (s, 3H), 2.17 (s, 3H), 1.77 (s, 6H), 1.29 (t, J = 7.2 Hz, 3H); ¹³C NMR

(CDC1₃, 75 MHz) δ 161.1, 152.6, 148.4, 139.5, 136.9, 135.0, 129.6, 128.5, 125.8,

123.7, 121.3115.3, 113.0, 110.1, 60.1, 21.1, 17.6, 16.6, 14.6; Mass spec: 362.10 (MH^4")

Intermediate 72

2-Ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza-cyclopentarα1indene-3- carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDCI₃, 300 MHz) δ 8.61 -

8.58 (m, IH), 7.30 - 7.23 (m, 2H), 7.03 (s, 2H), 6.91 - 6.88 (m, IH), 4.48 (q, J = 7.1 Hz, 3H), 3.03 (q, J = 7.5 Hz, 2H), 2.36 (s, 3H), 1.96 (s, 6H), 1.48 (t, J = 7.2 Hz, 3H), 1.28 (t, J = 7.4 Hz); Mass spec: 376.23 (MET^1") Intermediate 73

2-Trifluoromethyl-8-(2,4,6-trimethvI-phenyl)-8H-l,3a,8-triaza- cyclopentaralindene-3-carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above but in a sealed bomb (170°C, 60 h). 1H

NMR (CDCI₃, 300 MHz) δ 8.76 - 8.73 (m, IH), 7.43 - 7.34 (m, 2H), 7.08 (s, 2H),

7.01 - 6.98 (m, IH), 4.54 (q, J = 7.12 Hz, 2H), 2.39 (s, 3H), 1.99 (s, 6H), 1.50 (t, J =

7.2 Hz, 3H); ¹³C NMR (CDC1₃, 75 MHz) δ 159.1, 147.0, 139.9, 139.1 (q, J = 39.0 Hz), 136.9, 135.7, 129.7, 128.0, 125.4, 125.0, 121.9, 120.9 ( q, J = 268 Hz), 116.4, 110.6, 61.4, 21.0, 17.6, 14.0; Mass spec: 416.09 (MH^")

Intermediate 74

8-(2,4-Dichloro-phenyl)-2-methyl-8H-l,3a,8-triaza-cyclopentarfl]indene-3- carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.59 -

8.56 (m, IH), 7.64 (d, J = 2.0 Hz, IH), 7.53 (d, J = 8.5 Hz, IH), 7.44 (dd, J = 8.4, 2.1 Hz, IH), 7.31 - 7.24 (m, 2H), 7.02 - 6.99 (m, IH), 4.44 (q, J = 7.0 Hz, 2H), 2.62 (s,

3H), 1.45 (t, J = 7.1 Hz, 3H); ¹³C NMR (CDC1₃, 75 MHz) δ 161.0, 152.3, 148.4, 136.2, 135.0, 133.9, 131.1, 131.0, 130.5, 128.8, 126.1, 123.9, 122.1, 115.5, 113.5, 110.6, 60.3, 16.6, 14.6; Mass spec: 388.10 (MH^1").

Intermediate 75

8-(2,4-Dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentarαlindene-3-carboxyIic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above but in a sealed bomb (170°C, 60 h). 1H

NMR (CDC1₃, 500 MHz) δ 8.69 (d, J = 8.2 Hz, IH), 7.68 (d, J = 2.2 Hz, IH), 7.54 (d, J = 8.4 Hz, IH), 7.49 (dd, /= 8.5, 2.2 Hz, IH), 7.43 - 7.37 (m, 2H), 7.09 (d, J = 8.2 Hz, IH), 4.51 (q, / = 7.2 Hz, 2H), 1.47 (t, J = 7.2 Hz, 3H); Mass spec: 442.05 (MH^4").

Intermediate 76

8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cyclopentaFαlindene-3-carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above but in a sealed bomb (170°C, 60 h). Mass spec: 494.10 (MET^1"). Intermediate 77

2-Methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopenta[ ]indene-

3-carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example. 1H NMR (CDC1₃, 500 MHz) δ 8.77 (dd, J =

8.1, 1.2 Hz, IH), 8.29 (dd, J = 4.9, 1.2 Hz, IH), 7.23 (dd, J = 8.1, 5.0 Hz, IH), 7.04 (s, 2H), 4.48 (q, J = 7.1 Hz, 2H), 2.65 (s, 3H), 2.34 (s, 3H), 1.98 (s, 6H), 1.49 (t, J = 7.1 Hz, 3H). Mass spec: 363.22 (MET").

Intermediate 78

2-Ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cvclopenta[ lindene-3-

carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.78

(dd, J = 8.1, 1.4 Hz, IH), 8.28 (dd, J = 5.0, 1.4 Hz, IH), 7.23 (dd, J = 8.1, 5.0 Hz, IH), 7.04 (s, 2H), 4.49 (q, J = 7.1 Hz, 2H), 3.01 (q, J = 7.5 HZ, 2H), 2.34 (s, 3H), 1.98 (s, 6H), 1.47 (t, J = 7.1 HZ, 3H), 1.28 (t, J = 7.5 Hz, 3H). Mass spec: 377.20 (MH^4").

2-Trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-

cycIopentarα]indene-3-carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above but in a sealed bomb (170°C, 60 h). 1H

NMR (CDC1₃, 500 MHz) δ 8.93 (dd, J = 8.1, 1.4 Hz, IH), 8.41 (dd, J = 4.9, 1.4 Hz,

IH), 7.32 (dd, J = 8.1, 4.9 HZ, IH), 7.06 (s, 2H), 4.51 (q, J = 7.1 Hz, 2H), 2.36 (s, 3H), 1.98 (s, 6H), 1.47 (t, J = 7.1 Hz, 3H). Mass spec: 417.20 (MH^4").

Intermediate 80

8-(2-Chloro-4,6-dimethylphenyl)-2-methvI-8ff-1.3a,7,8-tetraaza-

cγclopentarαlindene-3-carboxylic acid ethyl ester, scheme 1: (F)

Prepared as described for the example above. 1H NMR (CDCI₃, 300 MHz) δ 8.78

(dd, J = 8.1, 1.4 Hz, IH), 8.29 (dd, J = 5.0, 1.5 Hz, IH), 7.26 (s, IH), 7.25 (dd, J = 8.1, 5.0 Hz, IH), 7.14 (s, IH), 4.48 (q, J = 7.2 Hz, 2H), 2.65 (s, 3H), 2.38 (s, 3H), 2.12 (s, 3H), 1.48 (t, J = 7.2 Hz, 3H). Mass spec: 383.16 (MH^4"). Intermediate 81

r2-Trifluoromethyl-8-(2,4,6-trimethyIphenyl)-8H-l,3a,8-triaza- cyclopenta[α1inden-3-vn-methanol, scheme 2: (I) To a solution of trifluoromethyl-trimethylphenyl-8H-l,3a,8-triaza- cyclopenta[ ]indene-3-carboxylic acid ethyl ester (2.5 lg, 6.05 mmol) in tetrahydrofuran (40 mL) was added LiAlE (1.0 M solution in ether, 18.2 mL, 18.2

mmol) at 0°C. The resulting clear solution was stirred at 0°C for 1 h and then

quenched at 0°C by the sequential additions of water (0.69 mL), 15% aq.NaOΗ (0.69

mL) and water (2.1 mL). The mixture was warmed up to room temperature and filtered through a pad of celite^®. After removing solvents in vacuo, the title

compound was obtained as an off-white solid (2.26 g, 100% yield), which was pure

by LC-MS and 1H NMR. 1H NMR (CDC1₃, 500 MHz) δ 7.97 (dd, J = 7.2, 1.8 Hz,

IH), 7.32 - 7.29 (m, 2H), 7.03 (s, 2H), 6.92 (dd, / = 7.2, 2.0 Hz, IH), 5.14 (s, 2H), 2.35 (s, 3H), 1.98 (s, 6H); Mass spec: 374.23 (MH^4").

Intermediate 82

r8-(2,4-Dichlorophenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza-cyclopenta[αlinden- 3-yll-methanol, scheme 2: (I)

To a solution of 8-(2,4-Dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopenta[α]indene-3-carboxylic acid ethyl ester (490 mg, 1.11 mmol) in methylene

chloride (20 mL), was added at 0°C a toluene solution of DIB AL-Η (5.55 mL, 5.55

mmol). After stirring at 0°C for 75 min, the reaction mixture was cooled down to -

78°C and methanol (2.2 mL) was added dropwise, followed by additions of ground

Na₂SO -10Η₂O (15.2 g) and celite (2.6 mL). The resulting mixture was warmed up to room temperature in 4 h. After filtration, the solvents were removed in vacuo to afford the title compound as an off white solid (443 mg, 100% yield). 1H NMR

(CDC1₃, 500 MHz) δ 8.00 - 7.93 (m, IH), 7.65 (d, J = 2.2 Hz, 1H0, 7.57 (d, J = 7.4 Hz, IH), 7.46 (dd, J = 8.6, 2.3 Hz, IH), 7.37 - 7.33 (m, 2H), 7.08 - 7.05 (m, IH); Mass spec: 400.02 (MH^4").

Intermediate 83

f8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyI-8H-l,3a,8-triaza-

cvclopentarα]inden-3-yπ-methanol, scheme 2: (I)

Prepared as the example shown above (DIB AL-H reduction) in 100% yield and used

for the next step without further purification. 1H NMR (CDC1₃, 300 MHz) δ 7.96 (d,

J = 8.9 Hz, IH), 7.65 (d, J = 1.8 Hz, IH), 7.46 (d, J = 8.1 Hz, IH), 7.36 -7.31 (m, 2H), 7.17 (d, J = 7.3 Hz, IH), 7.08 (d, J = 9.0 Hz, IH), 5.12 (s, 2H), 2.97 (sept, J = 6.9 Hz, IH), 2.36 (s, IH), 1.30 (d, J = 6.9 Hz, 6H); Mass spec: 454.07 (MH⁴").

Intermediate 84

[2-Methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopentar ]inden-3-

yl]-methanol, scheme 2: (I)

Prepared as the example shown above (DIB AL-H reduction). Mass spec: 321.20 (MH^1")

Intermediate 85

[2-Ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopenta[α1inden-3-

yl]-methanol, scheme 2: (I)

Prepared as the example shown above (DIBAL-H reduction). 1H NMR (CDC1₃, 300

MHz) δ 8.22 (dd, J = 5.1, 1.4 Hz, IH), 8.04 (dd, J = 7.9 Hz, IH), 7.16 (dd, J = 7.9,

5.1 Hz, IH), 7.03 (s, 2H), 4.95 (d, J = 4.6 Hz, 2H), 2.68 (q, J = 7.5 Hz, 2H), 2.36 (s, 3H), 2.02 (s, 6H), 1.25 (t, J = 7.5 Hz, 3H); Mass spec: 335.25 (MH ^"). Intermediate 86

F2-Trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-

cyclopenta[ ]inden-3-yll-methanol, scheme 2: (I) Prepared as the example shown above (DIBAL-H reduction). 1H NMR (CDC1₃, 500 MHz) δ 8.34 (dd, J = 5.0, 1.4 Hz, IH), 8.23 (dd, J = 8.0, 1.4 Hz, IH), 7.24 (dd, J= 8.0, 5.0 Hz, IH), 7.04 (s, 2H), 5.11 (s, 2H), 2.33 (s, 3H), 2.01 (s, 6H); Mass spec: 375.20 (MH^4").

Intermediate 87

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-

cyclopenta[ ]inden-3-vn-methanol, scheme 2: (I)

Prepared as the example shown above (DIBAL-H reduction). 1H NMR (CDC1₃, 300

MHz) δ 8.23 (dd, J = 5.1, 1.3 Hz, IH), 8.04n (dd, J = 7.9, 1.4 Hz, IH), 7.24 (s, IH), 7.17 (dd, J = 7.9, 5.1 Hz, IH), 7.11 (s, IH), 4.93 (s, 2H), 2.36 )s, 3H), 2.31 (s, 3H), 2.14 (s, 3H); Mass spec: 341.15 (MH^4"). Intermediate 88

3-Chloromethyl-2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cyclopenta[fl]indene:⁵, scheme 2: (J) A sealed tube containing (trifluoromethyl-trimethylphenyl-8H-l,3a,8-triaza- cyclopenta[α]inden-3-yl)-methanol (1.1 g, 2.95 mmol) and SOCl₂ (3.5 mL) was

heated at 80°C for 1 h. After removing SOCl₂ in vacuo, the title compound was

obtained as a light brown viscous liquid (1.15 g, 100% yield), which was pure by 1H NMR. 1H NMR (CDC1₃, 500 MHz) d 7.94 -7.92 ( , IH), 7.39 - 7.37 (m, 2H), 7.05 (s, 2H), 7.00 - 6.98 (m, IH), 5.18 (s, 2H), 2.37 (s, 3H), 1.99 (s, 6H); Mass spec. 388.30 [M - Cl + OMe + H]^4".

Intermediate 89

3-Chloromethyl-8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza-

cyclopentarαlindene, scheme 2: (J)

Prepared as the example shown above (SOCl₂ neat, 80°C, 30 min). Mass spec

414.08 [M - Cl + OMe + H]^4". Intermediate 90

8-(2-Bromo-4-isopropyl-phenyl)-3-chloromethyl-2-trifluoromethyl-8H-l,3a,8-

triaza-cyclopentarα]indene, scheme 2: (J)

Prepared as the example shown above (SOCl₂ neat, 80°C, 30 min). Mass spec.

466.10 [M - Cl + OMe + H]^4".

Intermediate 91

3-ChloromethyI-2-methyl-8-(2,4,6-trimethyl-phenvI)-8H-l,3a,7,8-tetraaza- cyclopentarαlindene:⁶, scheme 2: (J)

Thionyl chloride (0.164 mL, 2.25 mmol) was added at 0°C to a solution of [2-methyl-

8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopenta[ ]inden-3-yl]-methanol (0.36 g, 1.12 mmol) in CΗ₂C1₂ (10 mL). After 2h, solvents was removed and the title compound was obtained as a brownish oil (100% yield). Mass spec: 335.24 (M - Cl + OMe + H)⁺. Intermediate 92

3-Chloromethyl-2-ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-

cycIopenta[ ]indene, scheme 2: (J)

Prepared as the example shown above (SOCl₂, CH₂C1₂, 0 °C, 2h). Mass spec.

349.22 (M - Cl + OMe + H)^4".

Intermediate 93

3-Chloromethyl-2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8g-1.3a,7,8-

tetraaza-cyclopentar lindene, scheme 2: (J)

Prepared as the example shown above (SOCl₂, CH₂C1₂, 0 °C, 2h). Mass spec.

389.20 (M - Cl + OMe + H)^4".

Intermediate 94

8-(2-Chloro-4,6-dimethyl-phenyl)-3-chloromethyl-2-methyl-8H-l,3a,7,8-

tetraaza-cyclopentarαlindene, scheme 2: (J)

Prepared as the example shown above (SOCl₂, CH₂C1₂, 0 °C, 2h). Mass spec.

355.16 (M - Cl + OMe + H)⁺.

For Examples 139-141 and 143-149, LC/MS were run using the following

conditions: Column, YMC ODS S7 3.0x50 mm; run time, 3 mins. For Example

142, the LC/MS was run using the following conditions: Column, YMC C18 S5

4.6x50 mm; run time, 4 mins.

Example 139

5-FIuoro-2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-1.3a,8-triaza- cyclopentarαlindene-3-carboxylic acid cyclopropylmethyl-propyl-amide:⁷, scheme 1: (G)

A solution of trimethylaluminum (2.0 M in heptane, 1.4 mL, 2.8 mmol) was added to a solution of N-cyclopropylmethyl-N-propylamine (0.40 mL, 2.8 mmol) in benzene

(3 mL) at 0°C. The mixture was warmed up to room temperature and stirred at this

temperature for 1.5 hours, and then added to a stirred solution of 5-fluoro-2-methyl- 8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza-cyclopenta[α]indene-3-carboxylic acid ethyl ester (0.13 g, 0.35 mmol) in benzene (2.0 mL). The mixture was refluxed for 12 hours. Upon cooling at 0°C, 1 N sodium hydroxide (15 mL) was added dropwise

to the above mixture. The mixture was extracted with dicholoromethane (30 mL), and the organic layer was dried over anhydrous sodium sulfate. Solvents were removed in vacuo and the residue was subjected to chromatography using ethyl acetate/hexanes (3:7) as eluent to afford the title compound as an off-white solid

(0.156 g, 100% yield). 1H NMR (CDC1₃, 300 MHz) δ 7.60 (dd, J = 8.7, 2.5 Hz, IH),

6.99 (s, 2H), 6.92 (td, J = 9.0, 2.5 Hz, IH), 6.75 (dd, J = 8.8, 4.4 Hz, IH), 3.66 (t, J = 7.1 Hz, 2H), 3.46 (d, J = 6.9 Hz, 2H), 2.35 (s, 3H), 2.32 (s, 3H), 1.92 (s, 6H), 1.71 - 1.63 (m, 2H), 1.11 - 1.05 (m, IH), 0.88 (t, J = 7.2 Hz, 3H), 0.57 - 0.53 (m, 2H), 0.19

- 0.16 (m, 2H); ¹³C NMR (CDC1₃, 75 MHz) δ 163.6, 159.4, 156.3, 148.9, 143.3,

139.4, 137.0, 131.6, 129.7, 128.7, 124.8 (d, J = 13 Hz), 114.2, 110.6 (d, J = 25 Hz), 101.2 (d, J = 29 Hz), 51.3, 48.6, 21.1, 21.0, 17.8, 15.7, 11.3, 10.1, 3.8. LC/MS: to = 1.95 min, 447.22 (MH^4").

Example 140

2-Methyl-8-(2,4,6-trimethyl-phenyl)-8J -l,3a,8-triaza-cvclopentarα]indene-3- carboxylic acid cyclopropylmethyl-propyl-amide, scheme 1: (G)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.86 -

7.82 (m, IH), 7.23 - 7.19 (m, 2H), 7.02 (s, 2H), 6.89 -6.86 (m, IH), 3.69 (t, J = 7.0 Hz, 2H), 3.49 (d, J = 6.9 Hz, 2H), 2.39 (s, 3H), 2.35 (s, 3H), 1.98 (s, 6H), 1.74 - 1.65 (m, 2H), 1.16 - 1.06 (m, IH), 0.90 (t, J = 7.2 Hz, 3H), 0.59 - 0.53 (m, 2H), 0.23 - 0.20 (m, 2H); ¹³C NMR (CDC1₃, 75 MHz) δ 163.7, 147.9, 139.2, 137.0, 135.2, 129.5,

128.8, 124.8, 123.3, 121.0, 114.2, 113.1, 110.2, 60.3, 51.1, 21.0, 17.7, 15.4, 11.2, 10.1, 3.8; LC/MS: to = L95 min, 429.13 (MET^").

Example 141

2-Ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza-cyclopenta[ ]indene-3- carboxylic acid cyclopropylmethyl-propyl-amide, scheme 1: (G)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.81 - 7.76 (m, IH), 7.23 - 7.16 (m, 2H), 7.02 (s, 2H), 6.87 - 6.84 (m, IH), 3.68 (t, J = 6.6 Hz, 2H), 3.49 (d, J = 6.7 Hz, 2H), 2.70 (q, J = 7.4 Hz, 2H), 2.35 (s, 3H), 1.98 (s, 6H), 1.73 - 1.63 (m, 2H), 1.28 (t, J = 7.4 Hz, 3H), 1.15 - 1.05 (m, IH), 0.89 (t, J = 7.3 Hz, 3H), 0.57 - 0.54 (m, 2H), 0.25 - 0.20 (m, 2H); LC/MS: to = L95 min, 443.23 (MH^4").

Example 142

2-trifluoromethyl-8-(2,4,6-trimethylphenyl)-8H-l,3a.8-triaza- eyclopentaffllindene-3-carboxylic acid cyclopropy methyl-propyl-amide, scheme 1: (G) Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.72 -

7.66 (m, IH), 7.32 - 7.20 (m, 2H), 7.02 (s, 2H), 6.91 (d, J = 7.8 Hz, IH), 3.80 - 3.26 (m, 4H), 2.33 (s, 3H), 1.97 (s, 6H), 1.82 - 1.53 (m, 2H), 1.33 - 1.20 (m, IH), 1.04 (t, J = 7.2 Hz, 3H), 0.95 - 0.83 (m, 2H), 0.74 - 0.59 (m, 2H); LC/MS: to = 2.86 min, 483.30 (MET^").

Example 143

8-(2,4-DichIoro-phenyl)-2-methyl-8H^r-l,3a,8-triaza-cyclopenta[β]indene-3- carboxylic acid cyclopropylmethyl-propyl-amide, scheme 1: (G)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.82 -

7.79 (m, IH), 7.65 (d, J = 2.2 Hz, IH), 7.53 (d, J = 8.5 Hz, IH), 7.44 (dd, J = 8.5, 2.2 Hz, IH), 7.25 - 7.22 (m, 2H), 7.02 - 6.99 (m, IH), 3.68 (t, J = 7.0 Hz, 2H), 3.48 (d, J = 6.8 Hz, 2H), 2.38 (s, 3H), 1.75 - 1.63 (m, 2H), 1.13 - 1.07 (m, IH), 0.90 (t, J = 7.8 Hz, 3H), 0.59 - 0.53 (m, 2H)0.22 - 0.19 (m, 2H); LC/MS: to = 1-88 min, 455.11 (MH^4").

Example 144

2-Ethyl-5-fluoro-8-(2,4,6-trimethyl-phenvI)-8H-l,3a,8-triaza- cyclopenta[ ]indene-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 1: (G)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.58

(dd, J = 8.6, 2.5 Hz, IH), 7.02 (s, 2H), 6.95 (t, J = 9.6 Hz, IH), 6.79 - 6.76 (m,lH), 3.68 (t, J = 6.9 Hz, 2H), 3.49 (d, J = 6.8 Hz, 2H), 2.70 (q, J = 7.3 Hz, 2H), 2.35 (s, 3H), 1.98 (s, 6H), 1.73 - 1.63 (m,2H), 1.28 (t, J = 7.4 Hz, 3H), 1.15 - 1.10 (m, IH), 0.92 (t, J = 7.3 Hz, 3H), 0.59 - 0.54 (m 2H), 0.22 - 0.19 (m, 2H); ¹³C NMR (CDC1₃,

75 MHz) δ 163.7, 159.4, 156.2, 148.9, 139.4, 137.0, 131.6, 129.7, 128.8, 124.7 (d, J

= 9.0 Hz), 113.0, 110.5 (d, J = 11.4 Hz), 110.3, 101.0, 51.4, 48.7, 22.8, 21.1, 17.8, 13.8, 11.3, 10.1, 3.8; LC/MS: to = 2.05 min, 461.26 (MH ^").

Example 145

CycIopropyImethyl-r5-fluoro-2-methyl-8-(2,4,6-trimethvI-phenyl)-8H-l,3a,8- triaza-cyclopentarαlinden-3-ylmethyll-propyl-amine:⁸, scheme 1: (H)

A solution of Red-Al (3.3 M in toluene, 0.25 mL, 0.8 mmol) was added dropwise to a solution of 2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cyclopenta[fl]indene-3-carboxylic acid cyclopropylmethyl-propyl-amide (73 mg, 0.16

mmol) in toluene (2 mL) at 0 °C. After stirring at room temperature for 24 hours, the

reaction mixture was cooled to 0 ° C and 1 N sodium hydroxide (10 mL) was added

dropwise. The above mixture was extracted with dichloromethane (30 mL), and the organic extracts were washed with water and dried over anhydrous sodium sulfate. Solvents were removed in vacuuo and the residue was subjected to chromatography using ethyl acetate/hexanes as eluent to afford the title compound as a white solid

(59.4 mg, 86% yield). 1H NMR (CDC1₃, 300 MHz) δ 7.87 (dd, J = 9.1, 2.2 Hz, IH),

7.00 (s, 2H), 6.88 (td, J =- 9.0, 2.5 Hz, IH), 6.70 (dd, J = 8.8, 4.5 Hz, IH), 3.89 (s, 2H), 2.52 (t, J = 7.3 Hz, 2H), 2.46 (d, J = 6.6 Hz, 2H), 2.34 (s, 3H), 2.29 (s, 3H), 1.97 (s, 6H), 1.49 - 1.42 (m, 2H), 1.05 - 1.00 (m, IH), 0.74 (t, J = 7.3 Hz, 3H), 0.56 -

0.51 (m, 2H), 0.16 - 0.14 (m, 2H); ¹³C NMR (CDC1₃, 75 MHz) 8 159.3, 156.2, 148.3,

139.0, 138.8, 137.2, 130.5 (d, J = 179.5 Hz), 129.6, 125.4 (d, J = 13.0 Hz)115.8, 109.6, 109.3 (d, J = 25.8 Hz), 101.3 (d, J = 29.2 Hz), 59.0, 55.3, 48.8, 21.1, 19.7, 17.7, 13.8, 12.0, 8.7, 4.3; LC/MS: to = 1-57 min, 433.22 (MH*). Example 146

Cyclopropylmethyl-r2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza-

cvclopentaFα]inden-3-ylmethyl]-propyl-amine, scheme 1: (H)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.05 -

7.99 (m, IH), 7.18 - 7.12 (m, 2H), 6.94 (s, 2H), 6.80 -6.74 (m, IH), 3.96 (s, 2H), 2.52 (t, J = 6.8 Hz, 2H), 2.44 (d, J = 6.9 Hz, 2H), 2.36 (s, 3H), 2.30 (s, 3H), 1.98 (s, 6H), 1.50 - 1.44 (m, 2H), 1.05 - 0.98 (m, IH), 0.77 (t, J = 7.2 Hz, 3H), 0.55 - 0.50 (m, 2H), 0.16 - 0.12 (m 2H); LC/MS: to = L39 min, 415.23 (MH ^").

Example 147

Cvclopropylmethyl-r2-ethyl-8-(2.4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cvclopentafølinden-3-ylmethyll-propyl-amine, scheme 1: (H)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 8.05

8.01 (m, IH), 7.19 - 7.12 (m, 2H), 7.11 (s, 2H), 6.82 - 6.79 (m, IH), 3.93 (s, 2H), 2.65 (q, J = 7.5 Hz, 2H), 2.55 (t, J = 7.4 Hz, 2H), 2.48 (d, J = 6.6 Hz, 2H), 2.35 (s, 3H), 1.98 (s, 6H), 1.49 - 1.42 (m, 2H), 1.23 (t, J = 7.5 Hz, 3H), 1.08 - 0.98 (m, IH), 0.74 (t, J = 7.3 Hz, 3H), 0.53 - 0.49 (m, 2H), 0.13 - 0.10 (m, 2H); LC MS: to = 1.71 min, 429.25 (MH^4").

Example 148

Cyclopropylmethyl-propyl-(trifluoromethyl-trimethylphenyl-8H-l,3a,8- triaza-cyclopentarg]inden-3-ylmethyl)-amine, scheme 1: (H)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.37 -

7.33 (m, IH), 7.27 - 7.24 (m, IH), 7.16 (d, J = 7.4 Hz, IH), 7.04 (s, 2H), 6.97 - 6.94 (m, IH), 4.95 (s, 2H), 3.27 - 3.16 (m, 4H), 2.22 (s, 3H), 1.96 (s, 6H), 1.87 - 1.79 (m, 2H), 1.23 - 1.20 (m, IH), 0.97 (t, J = 7.2 Hz, 3H), 0.84 - 0.80 (m, 2H), 0.46 - 0.43 (m, 2H); LC MS: to = 1.57 min, 469.31 (MH^1").

Example 149

Cvclopropylmethyl-r2-ethyl-5-fluoro-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8- triaza-cyclopentar linden-3-ylmethyll-propyl-amine, scheme 1: (H)

Prepared as described for the example above. 1H NMR (CDC1₃, 300 MHz) δ 7.89

(dd, J = 9.1, 2.5 Hz, IH), 7.00 (s, 2H), 6.87 (td, J = 9.1, 2.6 Hz, IH), 6.69 (dd, J = 8.8, 4.5 Hz, IH), 3.90 (s, 2H), 2.63 (q, J = 7.5 Hz, 2H), 2.53 (t, J = 7.3 Hz, 2H), 2.47 (d, J = 6.6 Hz, 2H), 2.34 (s, 3H), 1.97 (s, 6H), 1.48 - 1.41 (m, 2H), 1.23 (t, J = 7.5 Hz, 3H), 1.05 - 0.95 (m, IH), 0.74 (t, J = 7.3 Hz, 3H), 0.56 - 0.52 (m, 2H), 0.15 - 0.12

(m, 2H); ¹³C NMR (CDC1₃, 75 MHz) δ 159.3, 156.1, 148.4, 145.1, 139.0, 137.2,

130.6 (d, J = 174 Hz), 129.6, 125.5 (d, J = 13.3 Hz), 115.0, 109.6, 109.2 (d, J = 24.8 Hz), 101.4 (d, J = 29.2 Hz), 59.1, 55.4, 48.8, 21.4, 21.1, 19.8, 17.8, 15.2, 12.0, 8.8, 4.3; LC/MS: to = L78 min, 447.27 (MH^1").

General Procedure for the Synthesis of Examples 150-282: (For Examples 150-252 LC/MS were run using the following conditions: Column,

YMC S5 4.6x50 mm; run time, 4 mins.)

An amine hydrochloride salt or a free amine (0.65 mmol, 5 equiv.) was added to an oven-dried 11 mL vial. After the addition of anhydrous acetonitrile (1 mL) and anhydrous z-Pr₂NEt (0.16 mL, 0.91 mmol, 7 equiv in the case of an amine-HCl salt,

or 43 μL, 0.26 mmol, 2 equiv in the case of a free amine), the mixture was stirred at

room temperature for 1 h, followed by the addition of a solution of a chloromethyl compound (0.13 mmol) in MeCN (1 mL). The resulting mixture was stirred at room

temperature for 24 h, or heated at 80 °C for 16 h if a trifluoromethyl-containing

amine hydrochloride salt was employed. After removing solvents and excess of i- Pr₂NEt in vacuo, the residue was dissolved in dimethylformamide or acetonitrile (2

mL) and CF₃CO₂H (30 μL) was added. The mixture (in most cases, a clear solution)

was filtered into a Prep-HPLC vial, and title compounds were obtained by Prep- HPLC.

Example 150

Cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-[2-trifluoromethyl-8-(2,4,6- trimethylphenyl-8H-l,3a,8-triaza-cyclopenta[α]inden-3-ylmethyll-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.99 min, 509.23 (MH ^").

Example 151

Bis-cyclopropylmethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8fl^r-

l,3a,8-triaza-cvclopenta[α]inden-3-ylmethvπ-amine. scheme 2: (H)

Prepared as described for the example above. LC/MS: t_R = 2.15 min, 481.28 (MH^4"). Example 152

Cyclopropylmethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-

triaza-cyclopenta[ 1inden-3-yImethyl1-(3,3,3-trifluoro-propyl)-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 2.86 min, 523.24 (MH^4").

Example 148

CyclopropyImethyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-

l,3a,8-triaza-cycIopentarα]inden-3-ylmethyll-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.57 min, 469.26 (MH^1").

Example 153

CvcIobutylmethyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-

l,3a,8-triaza-cyclopenta[α1inden-3-yImethyI]-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.28 min, 483.29 (MH^4").

Example 154

Cyclopropylmethyl-ethyl-r2-trifluoromethyl-8-(2,4,6-trimethyI-phenyl)-8fl^r-

l,3a,8-triaza-cyclopenta[ 1inden-3-ylmethyl]-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.06 min, 455.24 (MH^4").

Example 155

CycIopropylmethvI-(2,2,3,3,3-pentafluoro-propyl)-r2-trifluoromethyl-8-(2,4,6-

trimethyl-phenyl)-8H-l,3a,8-triaza-cvclopenta[a]inden-3-ylmethyl1-amine,

scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.06 min, 559.22 (MH^4").

Example 156

Cyclobutylmethyl-(2,2,2-trifluoro-ethyl)-[2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-8H-l,3a,8-triaza-cycIopentarα]inden-3-ylmethyI]-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 3.08 min, 523.23 (MH^4").

Example 157

Propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H^r-l,3a,8-triaza- cyclopentar 1inden-3-vImethyl1-(3,3,3-trifluoro-propyl)-amine, scheme 2: (H) Prepared as described for the example above. LC MS: to = 2.87 min, 511.23 (MH^1").

Example 158

(2,2,3,3,3-Pentafluoro-propyl)-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl- phenyI)-8H-l,3a,8-triaza-cycIopenta[ ]inden-3-ylmethyll-amine. scheme 2: (H) Prepared as described for the example above. LC/MS: to = 3.06 min, 547.22 (MH^4").

Example 159

Propyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,8-triaza-cyclopentar ]inden-3-ylmethyll-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 2.98 min, 497.23 (MH^4").

Example 160

Diallyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cyclopenta[α]inden-3-ylmethyll-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.26 min, 453.27.

Example 161

Phenethyl-propyI-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8- triaza-cyclopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.42 min, 519.44 (MH^4").

Example 162

(2,2,3,3,3-Pentafluoro-propyl)-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8- (2,4,6-trimethyI-phenyl)-8H-l,3a,8-triaza-cyclopentar 1inden-3-ylmethyl]- amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2:87 min, 551.18 (MET^1").

Example 163

Ethyl-phenethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8- triaza-cyclopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.31 min, 505.43 (MH^4").

Example 164

(2- Cyclopropyl-ethyD-propyl- r2-trifluoromethyl-8- (2,4,6- trimethvI-phenyl)-8H- l,3a,8-triaza-cyclopentar ]inden-3-ylmethyl1-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.25 min, 483.30 (MH ^").

Example 165

Benzyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza-

cyclopenta[ ]inden-3-ylmethyn-(3,3,3-trifluoro-propyI)-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 3.06 min, 559.24 (MH ^").

Example 166

(2-Cyclopropyl-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-

triaza-cycIopentar 1inden-3-ylmethyl]-(3,3,3-trifluoro-propyl)-amine, scheme 2:

(H) Prepared as described for the example above. LC/MS: to = 2.99 min, 537.25 (MH^").

Example 167

Benzyl-methyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyI)-8H-l,3a,8-triaza- cyclopentar 1inden-3-ylmethyl1-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.24 min, 477.25 (MH^4").

Example 168

Phenethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8-triaza- cyclopentar ]inden-3-ylmethyn-(3,3,3-trifluoro-propyI)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.10 min, 585.12 (MH^").

Example 169

(2-Cyclopropyl-ethyl)-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6- trimethyI-phenyI)-8iy-l,3a,8-triaza-cvclopentar ]inden-3-ylmethyn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 3.04 min, 523.24 (MH^4").

Example 170

Butyl-ethyl-r2-trifluoromethyI-8-(2,4,6-trimethyl-phenyl)-8H-l,3a.8-triaza- cyclopentar linden-3-ylmethyll-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.14 min, 457.26 (MH^4").

Example 171

Phenethyl-(2,2,2-trifluoro-ethyl)-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 8H-l,3a,8-triaza-cyclopenta[α]inden-3-ylmethyl]-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 3.06 min, 559.24 (MET^4").

Example 172

(2-Cvclopropyl-ethyl)-ethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,8-triaza-cyclopentar ]inden-3-yImethyl]-amine, scheme 2: (H) Prepared as described for the example above. LC/MS : to = 2.17 min, 469.29 (MH^4").

Example 173

Benzyl-ethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyI)-8H-l,3a,8-triaza-

cycIopenta[ ]inden-3-ylmethyI]-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.70 min, 491.26 (MH^4").

Example 174

Ethyl-phenethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,8- triaza-cyclopentarαlinden-3-ylmethvπ-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: t_R = 3.02 min, 505.43 (MET^4").

Example 175

Benzyl-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyI)-8H-l,3a,8-triaza- cyclopentar linden-3-ylmethvn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.46 min, 505.26 (MET^1"). Example 176

Benzyl'butyI-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a.8-triaza- cycIopentarα]inden-3-ylmethyn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.57 min, 519.27 (MH^4").

Example 177

Bis-cyclopropylmethyl- fS- (2,4-dichloro-phenyl)-2-trifluoromethyl-8H- 1 ,3a,8- triaza-cyclopentarα]inden-3-ylmethyll-amine, scheme 2: (H)

Prepared as described for the example shown above. LC/MS: t_R = 2.08 min, 507.15 (MH^4").

Example 178

Cyclopropylmethyl-[8-(2,4-dichloro-phenyl)-2-trifluoromethyI-8H-l,3a,8- triaza-cyclopenta[ ]inden-3-ylmethyI]-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.07 min, 495.17 (MH^4").

Example 179

CyclopropylmethyI-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8- triaza-cyclopenta[α1inden-3-ylmethyn-(2,2,2-trifluoro-ethyl)-amine, scheme 2:

(H) Prepared as described for the example above. LC/MS: to = 2.92 min, 535.09 (MH^4").

Example 180

CycIopropyImethyl-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-

triaza-cycIopenta[ linden-3-vImethyn-(3,3,3-trifluoro-propyl)-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: t_R - 2.76 min, 549.11 (MET^4").

Example 181

Cyclopropylmethyl-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8- triaza-cyclopentar 1inden-3-ylmethyl]-ethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-98 min, 481.13 (MH^4").

Example 182

[8-(2,4-Dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cvclopentar ]inden-3-ylmethyl]-phenethyl-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.39 min, 545.17 (MET^4").

Example 183

Cyclopropylmethyl-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8- triaza-cyclopenta[ ]inden-3-ylmethyl1-(2,2,3,3,3-pentafluoro-propyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: t_R = 2.99 min, 585.09 (MET^1").

Example 184

Diallyl-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopenta[α]inden-3-ylmethyn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.17 min, 479.14 (MH^1").

Example 185

Cyclobutylmethyl-r8-(2,4-dichloro-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopentar 1inden-3-yImethyl1-(2,2,2-trifluoro-ethyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.00 min, 549.12 (MH^4").

Example 186

Cyclobutylmethyl-r8-(2,4-dichloro-phenyI)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cyclopentar ]inden-3-ylmethyl]-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.18 min, 509.16 (MET^1").

Example 187

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentar linden-3-ylmethyll-bis-cyclopropylmethyl-amine, scheme 2: (H) Prepared as described for the example shown above. LC/MS: t_R = 2.29 min, 559.28 (MH^4").

Example 188

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentarα]inden-3-ylmethyI1-cyclopropylmethyl-(2,2,2-trifluoro-ethyI)-amine,

scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.04 min, 589.22 (MET^4").

Example 189

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentar ]inden-3-vImethyl]-cyclopropylmethyl-(3,3,3-trifluoro-propyl)- amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.87 min, 603.24 (MH^4").

Example 190

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopenta[ ]inden-3-ylmethvI1-cyclopropylmethyl-ethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.32 min, 535.26 (MH^4").

Example 191

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8 -^r-l,3a,8-triaza- cyclopentarα1inden-3-ylmethyn-cyclopropylmethyI-(2,2,3,3,3-pentafluoro- propyD-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.07 min, 639.22 (MET^4").

Example 192

Diallyl-[8-(2-bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cycIopenta[α1inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 2.39 min, 533.24 (MH^4").

Example 193

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopenta[ ]inden-3-ylmethyn-phenethyl-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.53 min, 599.30 (MH^4").

Example 194

[8-(2-Bromo-4-isopropyI-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentar ]inden-3-ylmethyn-cvclobutylmethyl-(2,2,2-trifluoro-ethyl)-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 3.09 min, 603.25 (MH^4").

Example 195

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-1.3a,8-triaza- cyclopentarα1inden-3-ylmethyl]-cvclobutylmethyl-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.38 min, 563.29 (MH^1").

Example 196 r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentar linden-3-ylmethyIl-ethyl-phenethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.42 min, 585.27 (MH^4").

Example 197

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopenta[oc]inden-3-ylmethyn-propyl-(3,3,3-trifluoro-propyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.88 min, 591.24 (MH^4").

Example 198

Allyl-[8-(2-bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cyclopenta[ ]inden-3-yImethyl1-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.29 min, 535.26 (MH^4").

Example 199

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopenta[α1inden-3-ylmethyl1-(4-fluoro-benzyl)-(3,3,3-trifluoro-propyl)-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 3.05 min, 657.22 (MH^4").

Example 200

[8-(2-Bromo-4-isopropyI-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopentar ]inden-3-ylmethyl]-propyl-(2,2,2-trifluoro-ethyl)-amine. scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 3.00 min, 577.23 (MH^4"). Example 201

F8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentarα]inden-3-ylmethyn-phenethyl-(2,2,2-trifluoro-ethyl)-amine, scheme

2: (H)

Prepared as described for the example above. LC/MS: to = 3.08 min, 639.24 (MH^4").

Example 202

Benzyl-r8-(2-bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopenta[α1inden-3-ylmethyll-(3,3,3-trifluoro-propyl)-amine. scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.06 min, 639.23 (MH^4").

Example 203 r8-(2-Bromo-4-isopropyI-phenyI)-2-trifluoromethyl-8H-l,3a,8-triaza-

cyclopentarα]inden-3-ylmethyl]-butyl-ethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.27 min, 537.27 (MH^4").

Example 204

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopenta[ 1inden-3-yImethyl]-(2-cyclopropyl-ethyl)-(2,2,2-trifluoro-ethyl)- amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.07 min, 603.24 (MH ^").

Example 205

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza-

cycIopenta[ ]inden-3-ylmethyI1-(2,2,3,3,3-pentafluoro-propyl)-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 3.06 min, 627.22 (MET^4").

Example 206

r8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cyclopentar ]inden-3-ylmethyl1-dipropyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.36 min, 537.20 (MH^4").

Example 207

[8-(2-Bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H-l,3a,8-triaza- cvclopentar 1inden-3-ylmethyn-(2-cyclopropyl-ethyl)-ethyl-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 3.52 min, 549.29 (MH^4"). Example 208

Benzyl-[8-(2-bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cyclopenta[ ]inden-3-yImethyl1-ethyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.43 min, 571.26 (MH^4").

Example 209

Benzyl-[8-(2-bromo-4-isopropyl-phenyl)-2-trifluoromethyl-8H^r-l,3a,8-triaza- cyclopentar ]inden-3-ylmethyn-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 2.47 min, 585.27 (MH^4").

Example 210

Cvclopropylmethyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cycIopentar 1inden-3-ylmethvn-amine,

scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.86 min, 510.23 (MH^4").

Cyclopropylmethyl-propyl-r2-trifluoromethyI-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,7,8-tetraaza-cyclopenta[a]inden-3-ylmethyl1-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.00 min, 470.26 (MET^4").

Example 212

Cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)-F2-trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.94 min, 560.21 (MH^4"). Example 213

Cyclopropylmethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[α]inden-3-ylmethyl1-(3,3,3-trifluoro-propyl)-amine, scheme

2: (H)

Prepared as described for the example above. LC/MS: to = 2.79 min, 524.24 (MH^4").

Example 214

Bis-cyclopropylmethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8f-^r- l,3a,7,8-tetraaza-cvclopenta[α]inden-3-ylmethvπ-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.01 min, 482.27 (MET^1").

Example 215

CvclobutylmethyI-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,7,8-tetraaza-cyclopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.18 min, 484.28 (MH^4").

Example 216

CyclobutvImethyl-(2.2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl- phenyI)-8fl^r-l,3a,7,8-tetraaza-cvclopentar 1inden-3-ylmethyl]-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.96 min, 524.24 (MH^4").

Example 217

PhenethyI-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopentarαlinden-3-ylmethyπ-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: t_R = 2.45 min, 520.27 (MH^4"). Example 218

Ethyl-phenethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopentar linden-3-ylmethyl]-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.27 min, 506.26 (MH^4").

Example 219

Diallyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cyclopentar ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.15 min, 454.24 (MET^1").

Example 220

Allyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[ ]inden-3-yImethvn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.03 min, 456.25 (MH^4").

Example 221

(4) Propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8g-l,3a,7,8-tetraaza- cyclopenta[α]inden-3-ylmethyn-(3,3,3-trifluoro-propyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.79 min, Mass spec: 512.24 (MH^1").

Example 222

Propyl-f2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4.6-trimethyl-phenyl)-

8H-l,3a,7,8-tetraaza-cvclopenta[ ]inden-3-ylmethyl]-amine. scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.84 min, 498.22 (MET^1"). Example 223

Cyclopropylmethyl-ethyI-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,7,8-tetraaza-cyclopentarα]inden-3-ylmethyl1-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.90 min, 456.25 (MH^4").

Example 224

(2,2,3,3,3-Pentafluoro-propyl)-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-8ff-l,3a,7,8-tetraaza-cyclopentarαlinden-3-ylmethyl]-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 2.94 min, 548.21 (MET^4").

Example 225

(2-Cvclopropyl-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,7,8-tetraaza-cyclopentar Xlmden-3-ylmethyn-(3,3,3-trifluoro-propyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.93 min, 538.26 (MET^4").

Example 226

Phenethyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cyclopenta[a]inden-3-ylmethyl]-(3,3,3-trifluoro-propyl)-amine scheme2:(H) Prepared as described for the example above. LC/MS: to = 2.99 min, 574.25 (MET^4").

Example 227

Benzyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8fl^r-1.3a,7,8-tetraaza-

cvcIopentaFαlinden-3-ylmethyl]-(3,3,3-trifluoro-propyl)-amine. scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.94 min, 560.23 (MH^4"). Example 228

Benzyl-methyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[ ]inden-3-ylmethyI1-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.08 min, 478.23 (MH^4").

Example 229

(2-Cyclopropyl-ethyl)-ethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H- l,3a,7,8-tetraaza-cyclopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.06 min, 470.27 (MH^4").

Example 230

(2-Cyclopropyl-ethyl)-propyl-[2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)- 8H-l,3a,7,8-tetraaza-cyclopenta[ ]inden-3-ylmethyl1-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.17 min, 484.28 (MH^4").

Example 231

Butyl-ethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopentarαlinden-3-ylmethvπ-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.01 min, 458.26 (MH^4").

Example 232

(2-CvcIopropyl-ethyl)-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6- trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cycIopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.94 min, 524.25 (MH^4"). Example 233

Benzyl-ethyl-r2-trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cycIopenta[ ]inden-3-ylmethyn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 2.16 min, 492.25 (MH^4").

Example 234

Phenethyl-(2,2,2-trifluoro-ethyl)-r2-trifluoromethyl-8-(2,4,6-trimethyl- phenyl)-8H^r-l,3a,7,8-tetraaza-cyclopentar 1inden-3-ylmethyn-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 2.96 min, 560.25 (MH ^").

Example 235

Benzyl-butyl-[2-trifluoromethyl-8-(2.4.6-trimethyl-phenyl)-8H-l,3a,7,8-

tetraaza-cyclopentarαlinden-3-yImethyll-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.56 min, 520.27 (MET^4").

Example 236

Benzyl-propyl-r2-trifluoromethyl-8-(2,4,6-trimethyI-phenyl)-8H-l,3a,7,8- tetraaza-cyclopentar ]inden-3-ylmethyI]-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.40 min, 506.26 (MH^4").

Example 237

Ethyl-r2-methyI-8-(2,4,6-trimethvI-phenyl)-8H-l,3a,7,8-tetraaza-

cyclopentar linden-3-ylmethyll-phenethyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-95 min, 452.28 (MH^4"). Example 238

Cvclobutylmethyl-[2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cyclopenta[α]inden-3-yImethyI1-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.84 min, 430.30 (MH^4").

Example 239

Diallyl-r2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cvclopentar ]inden-3-ylmethyn-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.66 min, 400.27 (MH^4").

Example 240

CyclopropyImethyl-r2-methyI-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-

tetraaza-cyclopepta[ ]inden-3-ylmethyll-propyI-amine. scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.68 min, 416.29 (MH^4").

Example 241

Bis-cvcIopropylmethyl-r2-methyl-8-(2.4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[α]inden-3-ylmethyn-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-84 min, 428.29 (MH^4").

Example 242

Allyl-r2-methyl-8-(2,4.6-trimethyl-phenyl)-8H-l,3a,7.8-tetraaza- cyclopenta[α1inden-3-ylmethyl]-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-65 min, 402.28 (MH^4").

Example 243

(2-Cvclopropyl-ethyl)-r2-methyl-8-(2,4,6-trimethyl-phenyl)-8g-l,3a,7,8- tetraaza-cvclopentarαlinden-3-ylmethyIl-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.84 min, 430.31 (MET^4").

Example 244

Cyclopropylmethyl-ethyl-r2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cvclopentaFα]inden-3-ylmethyl]-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-60 min, 402.28 (MH^4").

Example 245

Cyclobutylmethyl-r2-ethyl-8-(2.4.6-trimethyI-phenyl)-8fl^r-l,3a,7,8-tetraaza- cvclopentar linden-3-ylmethyl]-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.95 min, 444.33 (MH^4") Example 246

Bis-cyclopropylmethyl-[2-ethyl-8-(2,4,6-trimethyl-phenyl)-8H^r-l,3a,7,8- tetraaza-cyclopenta[ ]inden-3-yImethyl]-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-82 min, 442.31 (MH^4").

Example 247

CycIopropylmethyl-r2-ethyl-8-(2,4,6-trimethyl-phenyl)-8iy-l,3a,7,8-tetraaza- cyclopenta[κ]inden-3-ylmethyl1-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-68 min, 430.31 (MH^4").

Example 248

EthvH2-ethyl-8-(2A6-trimethyl-phenyl)-8H-1.3a,7,8-tetraaza- cycIopentarαlinden-3-ylmethyII-phenethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 2.05 min, 466.30 (MH^4").

Example 249

Allyl-r2-ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cyclopenta[α]inden-3-ylmethyl]-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.78 min, 416.29 (MH^4").

Example 250

Cvclopropylmethyl-ethyl-r2-ethvI-8-(2,4,6-trimethyl-phenyl)-8H-1.3a.7.8- tetraaza-cvcIopentarα]inden-3-ylmethyl]-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.70 min, 416.31 (MET^4"). Example 251

DiaIlyl-r2-ethyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza- cyclopentarαlinden-3-ylmethyll-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.79 min, 414.28 (MH^1").

Example 252

(2-Cvclopropyl-ethyl)-r2-ethyI-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[ ]inden-3-ylmethyll-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.95 min, 444.33 (MET^4").

For Examples 253-282 LC/MS were run using the following conditions: Column, YMC ODC S7 3.0x50 mm; run time, 3 min. Example 253

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopentara]inden-3-ylmethyl]-phenethyI-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-64 min, 486.27 (MH^4").

Example 254

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-

cyclopentarαlinden-3-ylmethyll-cvclobutylmethvI-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.54 min, 450.30 (MH^4").

Example 255

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cvcIopentaralinden-3-ylmethvH-ethvI-phenethyI-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.60 min, 472.24 (MH^4").

Example 256

8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-3-(3-phenyl-pyrrolidin-l- ylmethyI)-8H-l,3a,7,8-tetraaza-cvclopentaFα]indene, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.60 min, 470.20 (MH^4").

Example 257

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methvI-8H-l,3a,7.8-tetraaza- cycIopentar linden-3-ylmethyll-cyclopropylmethyl-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.47 min, 436.26 (MH^4"). Example 258

Allyl-F8-(2-chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cvcIopentarαlinden-3-ylmethyll-propyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-46 min, Mass spec. 422.30 (MH^4").

Example 259

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-1.3a.7.8-tetraaza- cvclopentar«]inden-3-ylmethyn-(2-cyclopropyl-ethyl)-propyl-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 1.55 min, 450.30 (MET^4").

Example 260

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-

cyclopenta[ 1inden-3-yImethyl]-dipropyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.45 min, 424.24 (MH^4").

Example 261

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cycIopentar linden-3-yImethyII-cyclobutylmethyl-ethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.51 min, 436.30 (MH^4").

Example 262

Dibutyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a.7,8-tetraaza- cvclopentarαlinden-3-ylmethyll-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-60 min, 452.29 (MET^4"). Example 263

Benzyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ ]inden-3-ylmethyn-propyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-59 min, 472.32 (MET^4").

Example 264

DialIyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[a]inden-3-ylmethvH-amine, scheme 2: (H)

Prepared as described for the example above. LC MS: to = 1-45 min, 420.25 (MET^").

Example 265

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a.7.8-tetraaza- cyclopenta[α]inden-3-ylmethyn-cyclopropylmethyI-ethyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-43 min, 422.22 (MH^4").

Example 266

Butyl-r8-(2-chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cycIopentar linden-3-ylmethyll-ethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.48 min, 424.30 (MET^4").

Example 267

3-(2-Benzyl-pyrrolidin-l-ylmethyl)-8-(2-chloro-4,6-dimethyI-phenyl)-2- methyl-SH-l^a ^-tetraaza-cvclopentaE lindene, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.62 min, 484.26 (MH^4"). Example 268

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ ]inden-3-ylmethyl]-(2-cyclopropyl-ethyl)-ethyl-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 1. 1 min, 436.32 (MH^4").

Example 269

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ 1inden-3-ylmethyll-diethyl-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1-36 min, 396.25 (MET^4").

Example 270

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-

cyclopentarα]inden-3-ylmethyl1-methyl-(2-pyridin-3-yl-ethyl)-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 1.31 min, 459.26 (MET^4").

Example 271

8-(2-Chloro-4,6-dimethyl-phenyI)-2-methyl-3-(2-phenyl-pyrrolidin-l- ylmethyD-SH-l^a ^-tetraaza-cycIopentar lindene, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.57 min, 470.24 (MH^4").

Example 272

3-(3-Benzyl-pyrrolidin-l-ylmethyl)-8-(2-chloro-4,6-dimethyl-phenyl)-2-

methyl-8ff-l,3a,7,8-tetraaza-cyclopenta[α]indene, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1-64 min, 484.24 (MET^1"). Example 273

8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-3-(3-phenethyl-pyrrolidin-l- ylmethyl)-8H-l,3a,7,8-tetraaza-cyclopentarα]indene, scheme 2: (H) Prepared as described for the example above. LC/MS: to = 1.71 min, 498.27 (MH^4").

Example 274

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopentarα1inden-3-ylmethyn-methyl-pyridin-4-ylmethyl-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 1.51 min, 445.22 (MH^4").

Example 275

8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-3-(2-phenethyl-pyrrolidin-l-

ylmethyl)-8H-l,3a,7,8-tetraaza-cycIopentar ]indene, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.66 min, 498.27 (MH^4").

Example 276

8-(2-ChIoro-4,6-dimethyl-phenyl)-2-methyl-3-morpholin-4-ylmethyl-8H- l,3a,7,8-tetraaza-cyclopentaFα1indene, scheme 2: (H) Prepared as described for the example above. LC/MS: t_R = 1.35 min, 410.25 (MH^1*).

Example 277

r8-(2-Chloro-4.6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopentar ]inden-3-ylmethyl1-methyl-pyridin-3-ylmethyl-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.34 min, 445.22 (MET^4"). Example 278

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ ]inden-3-ylmethyn-methyl-(2-pyridin-2-yl-ethyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.37 min, 459.20 (MH^4").

Example 279

F8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ 1inden-3-ylmethyl]-(l-ethyI-propyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.44 min, 410.30 (MET^4").

Example 280

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-

cyclopenta[ ]inden-3-ylmethyl1-methyl-(2-pyridin-4-yl-ethyl)-amine, scheme 2:

(H)

Prepared as described for the example above. LC/MS: to = 1.30 min, 459.26 (MH^4").

Example 281

[8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cyclopenta[ ]inden-3-ylmethyl1-bis-(2-methoxy-ethyl)-amine, scheme 2: (H) Prepared as described for the example above. LC/MS: t_R = 1.46 min, 456.27 (MH^4").

Example 282

r8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza- cvcIopentarfl1inden-3-ylmethvn-(2-methoxy-l-methoxymethyl-ethyl)-amine, scheme 2: (H)

Prepared as described for the example above. LC/MS: to = 1.44 min, 442.27 (MH^4").

The following Intermediates 95-112 may be used to synthesize Examples 283-300. Intermediate 95

2-Bromo-5-methyl-3-r(2,4,6-trimethyl-phenyIcarbamoyI)-methyl]-3H-imidazole- 4-carboxylic acid ethyl ester, scheme 5: (V)

To a solution of 2-bromo-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester (1.00 g, 4.291 mmol) and 2-bromo-N-(2,4,6-trimethyl-phenyl)-acetamide (1.209 g, 4.720 mmol) in a mixture of toluene (16 mL) and acetone (8 mL) was added diazabicycloundecene (0.71 mL, 4.720 mmol). The resulting solution was stirred at room temperature for 24 h. Methanol (10 mL) was added to dissolve the precipitate formed, followed by the addition of silica gel (25 g). The solvent was removed under reduced pressure to dryness and the residue was applied to a silica gel-packed column. The isolation of the product was achieved by column chromatography (hexanes - ethyl acetate 4:1 to 1:2). Yield - 0.736 g (42%). 1H NMR (DMSO d-6,

500 MHz) δ 9.52 (s, IH), 6.86 (s, 2H), 5.15 (br s, 2H), 4.25 (q, J = 7.1 Hz, 2H), 2.38

(s, 3H), 2.21 (s, 3H), 2.11 (s, 6H), 1.30 (t, J = 7.1 Hz, 3H); LC/MS: to = 1.46 min., MS: [M+H] = 408. Intermediate 96

2-Methyl-6-oxo-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5fl^r-imidazo[l,2- alimidazole-3-carboxyIic acid ethyl ester, scheme 5: (W) A suspension of 2-bromo-5-methyl-3-[(2,4,6-trimethyl-phenylcarbamoyl)-methyl]- 3H-imidazole-4-carboxylic acid ethyl ester (17.4 mg, 0.038 mmol) and silver

carbonate (11.6 mg, 0.042 mmol) in sulfolane (0.5 mL) was heated at 150°C for 4 h.

The resulting reaction mixture was cooled to room temperature and filtered through a short pad of celite. The final purification was achieved by a reverse-phase preparative ΗPLC to give the desired product as white solid. Yield - 12.2 mg (73%). 1H NMR

(DMSO d-6, 500 MHz) δ 7.04 (s, 2H), 4.99 (s, 2H), 4.26 (q, J = 7.2 Hz, 2H), 2.34 (s,

3H), 2.30 (s, 3H), 2.06 (s, 6H), 1.31 (t, J = 7.2 Hz, 3H); LC MS: to = 1-75 min., MS: [M+H] = 328.

Intermediate 97

6-Chloro-2-methyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2-a1imidazole-3- carboxylic acid ethyl ester, scheme 6: (AA)

A solution of 3-ethoxycarbonyl-2-methyl-6-oxo-7-(2,4,6-trimethyl-phenyl)-6,7- dihydro-5H-imidazo[l,2-a]imidazolium trifluoroacetate (22.2 mg, 0.050 mmol) in

phosphorus oxychloride (1 mL) was heated at 150°C for 48 h. The excess of

phosphorus oxychloride was removed under reduced pressure, the residue was dissolved in saturated aqueous solution of sodium bicarbonate (20 mL) and extracted

with ethyl acetate (5x20 mL). The combined organic extracts were dried with

MgSO₄. The solvent was removed under reduced pressure and the crude product was dried under pump vacuum overnight. Yield - 23.3 mg (99%). LC/MS: to = 1.93 min., MS: [M+Η] = 346.

Intermediate 98

2-Bromo-5-ethyl-3-[(2,4,6-trimethylphenylcarbamoyI)methyl]-3Η-imidazoIe-4- carboxylic acid ethyl ester, scheme 5: (V)

Prepared as described above for intermediate 95. MS: m/e 422 (M+H)^4".

Intermediate 99

2-Ethyl-6-oxo-7-(2,4,6-trimethylphenyl)-6,7-dihydro-5H-imidazon,2- a]imidazole-3-carboxylic acid ethyl ester, scheme 5: (W)

Prepared as described above for intermediate 96. MS: m/e 342 (M+H)^4".

Intermediate 100

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazon,2-a1imidazole-3- carboxylic acid ethyl ester, scheme 6: (A A) Prepared as described above for intermediate 97. MS: m e 360 (M+H)^4".

Intermediate 101

2-Bromo-3-r(2-chloro-4,6-dimethylphenylcarbamoyl)-methyl1-5-ethvI-3H- imidazole-4-carboxylic acid ethyl ester, scheme 5: (V) Prepared as described above for intermediate 95. MS: m/e 442 (M+H)⁴

Intermediate 102

7-(2-ChIoro-4,6-dimethylphenyl)-2-ethyl-6-oxo-6,7-dihydro-5H-imidazon.2- alimidazole-3-carboxyIic acid ethyl ester, scheme 5: (W)

Prepared as described above for intermediate 96. MS: m/e 362 (M+H)^4".

Intermediate 103

6-Chloro-7-(2-chloro-4,6-dimethylphenyl)-2-ethyI-7H-imidazori,2-a]imidazole-

3-carboxylic acid ethyl ester, scheme 6: (AA)

Prepared as described above for intermediate 97. MS: m/e 380 (M+H)^4".

Intermediate 104

2-Bromo-5-ethyl-3-r(2,4,6-trichlorophenylcarbamoyI)-methyI1-3H-imidazole-4- carboxylic acid ethyl ester, scheme 5: (V)

Prepared as described above for intermediate 95. MS: m/e 482 (M+H)^4".

Intermediate 105

2-Ethyl-6-oxo-7-(2,4,6-trichlorophenyl)-6,7-dihydro-5H-imidazo[l,2- a]imidazole-3-carboxylic acid ethyl ester, scheme 5: (W)

Prepared as described above for intermediate 96. MS: m/e 402 (M+H)^4".

Intermediate 106

6-Chloro-2-ethyl-7-(2,4,6-trichlorophenyl)-7H-imidazo[l,2-a]imidazole-3- carboxylic acid ethyl ester, scheme 6 : (AA) Prepared as described above for intermediate 97. MS: m/e 420 (M+H)^4".

Intermediate 107

2-Bromo-5-ethyl-3-[(2-bromo-4-isopropylphenylcarbamoyl)-methyl]-3H- imidazole-4-carboxylic acid ethyl ester, scheme 5: (V)

Prepared as described above for intermediate 95. MS: m/e 500 (M+H)^4".

Intermediate 108

2-Ethyl-6-oxo-7-(2-bromo-4-isopropylphenyl)-6,7-dihvdro-5H-imidazori,2- alimidazole-3-carboxylic acid ethyl ester, scheme 5: (W)

Prepared as described above for intermediate 96. MS: m/e 420 (M+H)^4".

Intermediate 109

6-Chloro-2-ethyl-7-(2-bromo-4-isopropylphenyl)-7H-imidazori,2-a]imidazole-3- carboxylic acid ethyl ester, scheme 6: (AA)

Prepared as described above for intermediate 97. MS: m/e 438 (M+H)^4".

Intermediate 110

2-Bromo-3-f(2,4-dichlorophenylcarbamoyl)-methyl]-5-ethyl-3H-imidazole-4- carboxylic acid ethyl ester, scheme 5: (V) Prepared as described above for intermediate 95. MS: m/e 448 (M+H)^4".

Intermediate 111

7-(2,4-Dichlorophenyl)-2-ethyl-6-oxo-6,7-dihydro-5H-imidazo[l,2-a]imidazole-3- carboxylic acid ethyl ester, scheme 5: (W)

Prepared as described above for intermediate 96. MS: m/e 368 (M+H)^4".

Intermediate 112

6-Chloro-7-(2,4-dichlorophenyl)-2-ethyl-7H-imidazon,2-a]imidazole-3- carboxylic acid ethyl ester, scheme 6: (AA) Prepared as described above for intermediate 97. MS: m/e 386 (M+H)^4".

Example 283

6-Chloro-2-methyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazon,2-a]imidazole-3- carboxylic acid cyclopropylmethyl-propyl-amide , scheme 6: (BB) To a solution of N-cyclopropylmethylpropylamine (0.22 mL, 1.530 mmol) in toluene

(1.5 mL) at 0°C was added 2.0M solution of trimethylaluminum in toluene (0.77 mL,

1.530 mmol). The clear solution was warmed to room temperature and stirred for 1 h. A solution of 6-chloro-2-methyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazole-3-carboxylic acid ethyl ester (32.2 mg, 0.098 mmol) in toluene (1.0 mL)

was added at 0°C via cannula. The reaction mixture was heated at 80°C for 2h. A

solution of Rochelle's salt (2.0 mL) was added carefully at 0°C and the mixture was

vigorously stirred for 30 min. The crude product was extracted with ethylacetate. The combined organic extracts were dried with MgSO . The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative

ΗPLC. Yield - 21.3 mg (42%). 1H NMR (CD₃CN, 500 MHz) δ 7.69 (s, IH), 7.16 (s,

2H), 3.59 (t, J = 7.3 Hz, 2H), 3.39 (d, J = 6.9 Hz, 2H), 2.39 (s, 3H), 2.37 (s, 3H), 2.05 (s, 6H), 1.68 (sextet, J = 7.3 Hz, 2H), 1.11 (m, IH), 0.90 (t, J = 7.3 Hz, 3H), 0.60 (m, 2H), 0.23 (m, 2H); LC/MS: to = 1.71 min., MS: [M+H] = 413.

Example 284

[6-Chloro-2-methyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2-a]imidazol-3- ylmethyll-cyclopropylmethyl-propyl-amine, scheme 6: (DD) A solution of 3-(cyclopropylmethyl-propyl-carbamoyl)-2-methyl-6-oxo-7-(2,4,6- trimethyl-phenyl)-6,7-dihydro-5H-imidazo[l,2-a]imidazole (31.7 mg, 0.077 mmol) in toluene (3 mL) was added a 65% solution of Red-Al in toluene (0.12 mL, 0.384 mmol). The reaction mixture was stirred at room temperature for 14 h. A solution of

Rochelle's salt (2.0 mL) was added carefully at 0°C and the mixture was vigorously

stirred for 30 min. The crude product was extracted with ethylacetate. The combined organic extracts were dried with Na₂SO₄. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative HPLC.

Yield - 25.2 mg (64%). 1H NMR (CD₃OD, 500 MHz) δ 8.09 (s, IH), 7.19 (s, 2H),

4.75 (s, 2H), 3.31 (t, J = 6.5 Hz, 2H), 3.24 (d, J = 7.2 Hz, 2H), 2.44 (s, 3H), 2.39 (s, 3H), 2.06 (s, 6H), 1.24 (m, 3H), 1.05 (t, J = 7.4 Hz, 3H), 0.85-0.82 (m, 2H), 0.50 (m, 2H); LC/MS: to = 1.43 min., MS: [M+H] = 399.

Example 285

: 6-Chloro-2-ethyI-7-(2-bromo-4-isopropylphenyl)-7H-imidazoπ,2-a]imidazole-

3-carboχylic acid N-cyclopropylmethyl-N-propylamide. scheme 6: (BB)

Prepared as described for Example 283. IR(ιilm): 1615 cm^"1. 1H NMR (CDC1₃) δ

7.57 (d, J= 2.0 Hz, IH), 7.36 (d, J= 8.1 Hz, IH), 7.29 (dd, J= 8.1, 2.0 Hz, IH), 7.22 (s, IH), 3.60 (t, J= 7.1 Hz, 2H), 3.39 (d, J= 7.1 Hz, 2H), 2.95 (m, IH), 2.66 (q, J =7.6 Hz, 2H), 1.64 (m, 2H), 1.55 (s, 3H), 1.40 (s, 3H), 1.23 (t, J= 7.1 Hz, 3H), 0.88 (t, J= 7.1 Hz, 3H), 0.54 (m, 2H), 0.17 (m, 2H). MS: m/e 505(M+H)⁺.

Example 286

: 6-Chloro-2-ethyl-7-(2,4-dichlorophenyl)-7H-imidazon,2-alimidazole-3- carboxylic acid N-cyclopropylmethyl-N- (2,2,2- trifluoroethvDamide, scheme 6: (BB)

Prepared as described for Example 283. IR(film): 1630 cm^"1. 1H NMR (CDC1₃) δ

7.60 (m, IH), 7.42 (m, 2H), 7.27 (s, IH), 4.41 (q, J= 9.1 Hz, 2H), 3.52 (d, J= 6.6 Hz, 2H), 2.66 (q, J= 7.6 Hz, 2H), 1.23 (t, J= 7.6 Hz, 3H), 0.94 (m, IH), 0.60 (m, 2H), 0.16 (m, 2H). MS: m/e 493 (M+H)^4".

Example 287

: 6-Chloro-2-ethyl-7-(2,4-dichlorophenyl)-7H-imidazori,2-a1imidazole-3- carboxylic acid N,N-dipropylamide, scheme 6: (BB)

Prepared as described for Example 283. IR(film): 1615 cm^"1. 1H NMR (CDC1₃) δ 7.59 (m, IH), 7.41 (m, 2H), 7.24 (s, IH), 3.47 (t, J= 7.1 Hz, 4H), 2.65 (q, J= 7.6 Hz, 2H), 1.62 (m, 4H), 1.24 (t, J= 7.6Hz, 3H), 0.87 (t, J= 7.1Hz, 6H). MS: m/e 441 (M+H)^4".

Example 288

: 3-r(N,N-Dipropylamino)methvn-6-chloro-2-ethyl-7-(2,4-diclorophenyl)-7H- imidazori,2-a]imidazole, scheme 6: (DD)

Prepared as described for Example 284.

1H NMR (DMSO-d₆) δ 7.98 (m, IH), 7.89 (m, 1H), 7.70 (m, 2H), 4.52 (s, 2H), 3.00 (q, J= 7.6 Hz, 4H), 2.55 (q, J= 7.6 Hz, 2H), 1.68 (m, 4H), 1.12 (t, J= 7.6Hz, 3H), 0.89 (t, J= 7.6Hz, 6H). MS: m/e 427 (M+H)⁺. Example 289

: 3-r(N-Cyclopropylmethyl-N-(2,2,2-trifluoroethyl)amino)methyl]-6-chloro-2- ethyl-7-(2,4-diclorophenyl)-7H-imidazo[l,2-a]imidazole, scheme 6: (DD)

Prepared as described for Example 284. 1H NMR (CDC1₃) δ 7.62 (d, J= 2.0 Hz, IH),

7.53 (d, J= 8.6 Hz, IH), 7.47 (dd, J= 8.6, 2.0 Hz, IH), 7.42 (s, IH), 3.97 (s, 2H), 3.26 (q, J= 9.6 Hz, 2H), 2.69 (q, J= 7.6 Hz, 2H), 2.57 (q, J= 6.6 Hz, IH), 2.47 (q, J= 7.1 Hz, IH), 1.26 (t, J= 7.6 Hz, 3H), 0.86 (m, IH), 0.59 (m, 2H), 0.12 (m, 2H). MS: m/e 479 (M+H)^4".

Example 290

6-Chloro-2-ethyl-7-f2,4,6-trimethylphenyl)-7H-imidazon,2-a]imidazoIe-3- carboxylic acid N-cyclopropylmethyl-N-propylamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.26 (s, IH),

6.98 (s, 2H), 3.60 (t, J= 7.1 Hz, 2H), 3.39 (d, J= 7.1 Hz, 2H), 2.65 (q, J= 7.6 Hz, 2H), 2.32 (s, 3H), 2.01 (s, 6H), 1.64 (m, 3H), 1.22 (t, J= 7.6 Hz, 3H), 0.88 (m, 3H), 0.54 (m, 2H), 0.16 (q, J= 4.6, 6.1 Hz, 2H). MS: m/e: 427 (M+H)^4".

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazon,2-a]imidazole-3- carboxylic acid N-butyl-N-ethylamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.26 (s, IH), 6.98 (s, 2H), 3.53 (m, 4H), 2.65 (q, J= 7.1 Hz, 2H), 2.32 (s, 3H), 2.01 (s, 6H), 1.58 (m, 4H), 1.25 (m, 6H), 0.87 (t, J= 7.1 Hz, 3H). MS: m/e: 415 (M+H)⁺.

Example 292

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazori.2-alimidazole-3- carboxylic acid N,N-dipropylamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.29 (s, IH), 7.02 (s, 2H), 3.50 (t, J= 7.1 Hz, 4H), 2.69 (q, J= 7.1, 7.6 Hz, 2H), 2.36 (s, 3H), 2.05 (s, 6H), 1.64 (m, 4H), 1.26 (t, J= 7.6 Hz, 3H), 0.91 (overlapping d, J= 7.1, 7.6 Hz, 6H). MS: m/e: 415 (M+H)^4".

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazo[1.2-alimidazole-3- carboxylic acid N,N-diethylamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.28 (s, IH),

6.98 (s, 2H), 3.56 (q, J= 7.1 Hz, 4H), 2.65 (q, J= 7.6 Hz, 2H), 2.32 (s, 3H), 2.01 (s, 6H), 1.21 (m, 9H). MS: m e: 387 (M+H)^4".

3-r(N-Butyl-N-ethylamino)methyl1-6-chloro-2-ethyl-7-(2.4.6-trimethylphenyl)- 7H-imidazo[l,2-a]imidazole, scheme 6: (DD)

Prepared as described for Example 284. 1H NMR (CDC1₃, 400 MHz) δ 7.99 (s, IH),

7.11 (s, 2H), 4.54 (d, J= 4.6 Hz, 2H), 3.09 (m, 4H), 2.59 (q, J= 7.58 Hz, 2H), 2.33 (s, 3H), 1.93 (s, 6H), 1.61 (m, 2H), 1.29 (m, 6H), 1.13 (t, J= 7.6 Hz, 3H), 0.89 (dd, J= 7.1, 7.6 Hz, 3H). MS: m/e: 401 (M+H)^4".

Example 295

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazo[l,2-a]imidazole-3- carboxylic acid N,N-diallyIamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.20 (s, IH),

6.93 (s, 2H), 5.77 (m, 2H), 5.17 (m, 4H), 4.07 (d, J= 6.1 Hz, 4H), 2.62 (dd, J= 7.1, 7.6 Hz, 2H), 2.27 (s, 3H), 1.96 (s, 6H), 1.17 (t, J= 7.6 Hz, 3H). MS: m/e: 411 (M+H)^4".

Example 296

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazori,2-alimidazole-3- carboxylic acid N-cyclopropylmethyl-N-(2,2,2-trifluoroethyl)amide, scheme 6: (BB) Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.27 (s, IH),

6.99 (s, 2H), 4.41 (q, J= 9.1 Hz, 2H), 3.53 (d, J= 7.1 Hz, 2H), 2.66 (q, J= 7.6 Hz, 2H), 2.33 (s, 3H), 2.01 (s, 6H), 1.22 (t, J= 7.6 Hz, 3H), 0.93 (m, 1H), 0.59 (m, 2H), 0.15 (dd, J= 4.6, 6.1 Hz, 2H). MS: m/e: 467 (M+H)^4".

6-Chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazon.2-alimidazole-3- carboxylic acid N-ethyl-N-(pyridin-4-yl)methylamide, scheme 6: (BB) Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 8.58 (m, 2H),

7.32 (s, IH), 7.22 (d, J= 6.1 Hz, 2H), 6.98 (s, 2H), 4.74 (s, 2H), 3.54 (dd, J= 7.1, 7.6 Hz, 2H), 2.68 (dd, J = 7.1, 7.6 Hz, 2H), 2.32 (s, 3H), 2.01 (s, 6H). 1.21 (m, 6H). MS: m/e: 450 (M+H)^4".

6-ChIoro-2-ethyl-7-(2,4,6-trimethyIphenyl)-7H-imidazori,2-a1imidazole-3- carboxylic acid N-cyclopropylmethyl-N-ethylamide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.27 (s, IH),

6.97 (s, 2H), 3.69 (q, J= 7.1 Hz, 2H), 3.40 (d, J= 6.6 Hz, 2H), 2.65 (dd, J = 7.1, 7.6 Hz, 2H), 2.32 (s, 3H), 2.01 (s, 6H), 1.22 (t, J= 7.1 Hz, 6H), 1.03 (m, IH), 0.55 (m, 2H), 0.18 (dd, J= 5.1, 5.6 Hz, 2H). MS: m/e: 413 (M+H)^4".

3-[(N-CvcIopropylmethyl-N-ethylamino)methvn-6-chloro-2-ethyl-7-(2,4,6- trimethylphenyl)-7H-imidazoπ,2-a]imidazole, scheme 6: (DD)

Prepared as described for Example 284. 1H NMR (CDC1₃, 400 MHz) δ 7.92 (s, IH),

7.02 (s, 2H), 4.46 (s, 2H), 3.34 (s, 2H), 3.10 (d, J= 7.1 Hz, 2H), 2.74 (m, 2H), 2.34 (s, 3H), 1.97 (s, 6H), 1.41 (t, J= 7.1 Hz, 3H), 1.29 (t, J= 7.1 Hz, 3H), 1.13 (m, IH), 0.86 (m, 2H), 0.46 ( , 2H). MS: m/e: 399 (M+H)^4".

Example 300

6-Chloro-2-ethyI-7-(2,4,6-trimethylphenyl)-7H-imidazori,2-a1imidazole-3- carboxylic acid (3,5-dimethylpiperidin-l-yl)amide, scheme 6: (BB)

Prepared as described for Example 283. 1H NMR (CDC1₃, 400 MHz) δ 7.18 (s, IH),

6.90 (s, 2H), 4.12 (m, 2H), 2.57 (q, J= 7.6 Hz, 2H), 2.36 (t, J= 11.6, 12.6 Hz, 2H), 2.25 (s, 3H), 1.94 (s, 6H), 1.70 (m, 4H), 1.14 (t, J= 7.1, 7.6 Hz, 3H), 0.84 (d, J= 6.6 Hz, 4H), 0.78 (m, 2H). MS: m/e: 427 (M+H)^4".

Intermediates 95 and 96 were used to synthesize Example 301.

Example 301

2-Methyl-6-oxo-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H^r-imidazo[l,2- a]imidazole-3-carboxyIic acid cyclopropylmethyl-propyl-amide. scheme 7: (LL) To a solution of N-cyclopropylmethylpropylamine (0.22 mL, 1.530 mmol) in toluene

(1.5 mL) at 0°C was added 2.0M solution of trimethylaluminum in toluene (0.77 mL,

1.530 mmol). The clear solution was warmed to room temperature and stirred for 1 h. A solution of 6-chloro-2-methyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazole-3-carboxylic acid ethyl ester (20.0 mg, 0.058 mmol) in toluene (1.5 mL)

was added at 0°C via cannula. The reaction mixture was heated at 80°C for 2h. A

solution of Rochelle's salt (2.0 mL) was added carefully at 0°C and the mixture was

vigorously stirred for 30 min. The crude product was extracted with ethyl acetate. The combined organic extracts were dried with MgSO₄. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase

preparative ΗPLC. Yield - 3.6 mg (12%). 1H NMR (CD₃CN, 500 MHz) δ 7.07 (s,

2H), 4.73 (s, 2H), 3.57 (t, J = 7.1 Hz, 2H), 3.37 (d, J = 6.9 Hz, 2H), 2.35 (s, 3H), 2.19 (s, 3H), 2.14 (s, 6H), 1.65 (sextet, J = 7.3 Hz, 2H), 1.08 (m, IH), 0.90 (t, J = 7.4 Hz, 3H), 0.56 (m, 2H), 0.21 (m, 2H); LC/MS: to = 1-67 min., MS: [M+H] = 395.

The following Intermediates 113-115 may be used to synthesize Examples 302 and 303.

Intermediate 113

2-Bromo-5-trifluoromethyl-3-r(2,4,6-trimethyl-phenylcarbamoyl)-methyn-3H- imidazole-4-carboxylic acid ethyl ester, scheme 5: (V)

To a solution of 2-bromo-5-trifluoiOmethyl-3H-imidazole-4-carboxylic acid ethyl ester (3.00 g, 10.45 mmol) and 2-bromo-N-(2,4,6-trimethyl-phenyl)-acetamide (2.94 g, 11.50 mmol) in a mixture of toluene (16 mL) and acetone (8 mL) was added DBU (1.72 mL, 11.50 mmol). The resulting solution was stirred at room temperature for 5 days. Methanol (10 mL) was added to dissolve the precipitate formed, followed by the addition of silica gel (25 g). The solvent was removed under reduced pressure to dryness and the residue was applied to a silica gel-packed column. The isolation of the product was achieved by column chromatography (hexanes-ethyl acetate 4: 1). Yield -4.25 g (88%). LC/MS: to = 1.62 min., MS: [M+H] = 462.

Intermediate 114

2-Bromo-5-trifluoromethyl-3-[(2,4,6-trimethyl-phenylcarbamoyl)-methyn-3H- imidazole-4-carboxylic acid ethyl ester, scheme 5: (W)

A suspension of 2-bromo-5-trifluoromethyl-3-[(2,4,6-trimethyl-phenylcarbamoyl)- methyl]-3H-imidazole-4-carboxylic acid ethyl ester (20.12 g, 0.044 mmol) and silver

triflate (11.87 g, 0.046 mol) in sulfolane (200 mL) was heated at 150°C for 6 h. The

resulting reaction mixture was cooled to room temperature and filtered through a short pad of celite. The final purification was achieved by a reverse-phase preparative HPLC to give the desired product as yellowish solid. Yield - 5.24 g (24%). LC/MS: to = 1.89 min., MS: [M+H] = 382.

Intermediate 115

6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazoπ,2- a]imidazole-3-carboxylic acid ethyl ester, scheme 6: (AA) A solution of 6-oxo-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-6,7-dihydro-5H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester (3.04 g, 6.137 mol) in

phosphorus oxychloride (70 mL) was heated at 150°C for 72 h. The excess of phosphorus oxychloride was removed under reduced pressure, the residue was dissolved in saturated aqueous solution of sodium bicarbonate (100 mL) and

extracted with ethyl acetate (5x50 mL). The combined organic extracts were dried

with MgSO . The solvent was removed under reduced pressure and the crude product was dried under pump vacuum overnight. Yield - 1.192 g (38%). LC/MS: to = 2.17 min., MS: [M+Η] = 400. Example 302

6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyI-phenyl)-7H-imidazo[l,2- alimidazole-3-carboxylic acid cyclopropylmethyl-propyl-amide, scheme 6: (BB) To a solution of N-cyclopropylmethylpropylamine (0.22 mL, 1.530 mmol) in toluene

(1.5 mL) at 0°C was added 2.0M solution of trimethylaluminum in toluene (0.77 mL, 1.530 mmol). The clear solution was warmed to room temperature and stirred for 1 h. A solution of 6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazole-3-carboxylic acid ethyl ester (37.7 mg, 0.094 mmol) in toluene (1.0 mL)

was added at 0°C via cannula. The reaction mixture was heated at 80°C for 2h. A

solution of Rochelle's salt (2.0 mL) was added carefully at 0°C and the mixture was

vigorously stirred for 30 min. The crude product was extracted with ethyl acetate. The combined organic extracts were dried with MgSO₄. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative ΗPLC. Yield - 39.5 mg (90%). LC MS: to = 1.93 min., MS: [M+Η] = 467. Example 303

r6-Chloro-2-trifluoromethvI-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- alimidazoI-3-ylmethyll-cyclopropylmethyl-propyl-amine, scheme 6: (DD) A solution of 6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazole-3 -carboxylic acid cyclopropylmethyl-propyl-amide (27.2 mg, 0.058 mmol) in toluene (3 mL) was added a 65% solution of Red-Al in toluene (0.10 mL, 0.320 mmol). The reaction mixture was stirred at room temperature for 14 h. A

solution of Rochelle's salt (2.0 mL) was added carefully at 0°C and the mixture was vigorously stirred for 30 min. The crude product was extracted with ethyl acetate. The combined organic extracts were dried with Na₂SO₄. The solvent was removed under reduced pressure and the crude product was purified by a reverse-phase preparative ΗPLC. Yield- 12.8 mg (39%). LC/MS: to = 1-77 min., MS: [M+Η] = 453.

The following Intermediates 116 and 117 may be used to synthesize Examples 303- 347. Intermediate 116

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazon,2- alimidazoI-3-vI1-methanol, scheme 6: (CC) To a solution of 6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H- imidazo[l,2-a]imidazole-3-carboxylic acid ethyl ester (978.3 mg, 1.904 mmol) in tetrahydrofuran (100 mL) at 0°C was added a l.OM solution of lithium aluminum hydride in tetrahydrofuran (5.71 mL, 5.71 mmol). The resulting solution was stirred at 0°C for 10 min. Acetone (5 mL) was added and the solution was aded via cannula to a vigorously stirred ice-cold solution of Rochelle's salt (100 mL). The product was

extracted with ethyl acetate (5x50 mL) and the combined organic extracts were dried

over anhydrous Na₂SO . The solvent was removed in vacuo and the crude mixture was chromatographed on short silica gel column (hexanes - ethyl acetate 4:1) to give the desired product (614.8 mg, 90%) which was pure by LC-MS. LC/MS: to = 1.25 min., MS: [M+Η] = 358.

Intermediate 117

2-ChIoro-5-chloromethyl-6-trifluoromethyl-l-(2,4.6-trimethyl-phenyl)-lfl^"- imidazo[l,2-a]imidazole

A solution of [6-chloro-2-trifluoromethyl-7-(2,4,6-trimemyl-phenyl)-7H- imidazo[l,2-a]imidazol-3-yl]-methanol (614.8 mg, 1.718 mmol) and thionyl chloride (1.25 mL) in dichloromethane was stirred at 0°C for 15 min. Thionyl chloride and the solvent were removed in vacuo and the residue was dried under high vacuum to yield the desired product as a yellow solid (646.3 mg, 100%). LC/MS: to = 1.46 min., MS: [MΗ-Cl+OMe] = 373.

Example 303

r6-ChIoro-2-trifluoromethyl-7-(2,4,6-trimethvI-phenyl)-7Η-imidazori,2- alimidazol-3-ylmethyll-cvclopropylmethyl-propyl-amine. scheme 6: (DD)

To a solution of amine (6.1 mg, 0.054 mmol) and Ηύnig's base (0.05 mL) in acetonitrile (0.5 mL) at room temperature was added slowly a solution of 2-chloro-5- chloromethyl-6-trifluoromethyl-l-(2,4,6-trimethyl-phenyl)-lH-imidazo[l,2- a]imidazole (10.0 mg, 0.027 mmol) in acetonitrile (0.5 mL). The reaction mixture was stirred overnight. The final purification was achieved by a reverse-phase preparative ΗPLC to give the desired product as colorless oil. Yield - 9.9 mg (65%). LC/MS: to = 1.77 min., MS: [M+Η] = 453. Example 304

r6-Chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7g-imidazori,2- a1imidazol-3-ylmethyn-cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.31 min., MS: [M+H] = 494.

Example 305

2-ChIoro-5-(3.6-dihvdro-2g-pyridin-l-ylmethyl)-6-trifluoromethyl-l-(2,4.6- trimethyl-phenyl -lH-imidazori.2-a1imidazole, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.59 min., MS: [M+H] 423. Example 306

2-Chloro-5-thiomorphohn-4-ylmethyl-6-trifluoromethyl-l-(2,4,6-trimethyl- phenyl)-lH-imidazon,2-a1imidazoIe, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.63 min., MS: [M+H]

443.

Benzyl-r6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7g-imidazori,2- alimidazoI-3-ylmethyll-methyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.73 min., MS: [M+H] = 461.

[6-Chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7fl^r-imidazori,2- alimidazol-3-ylmethyll-methyI-phenethyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.76 min., MS: [M+H] 475.

Example 309

Benzyl-r6-chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7H-imidazoπ,2- a]imidazol-3-yImethyl]-ethyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.77 min., MS: [M+H] = 475. Example 310

Butyl-r6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7Jy-imidazon,2- alimidazol-3-ylmethyll-methyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = L62 min., MS: [M+H] =

427.

Example 311

Benzyl-butyl-r6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H- imidazori,2-alimidazoI-3-vImethyl1-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = L92 min., MS: [M+H] 503. - o -

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7g-imidazon.2- a1imidazol-3-ylmethvn-ethyl-(2-methyl-alIyl)-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.70 min., MS: [M+H] 439.

Example 313

r6-ChIoro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7g-imidazori,2- a1imidazol-3-ylmethyl1-(4-nitro-benzyl)-propyl-amine. scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.16 min., MS: [M+H] 534. Example 314

r6-Chloro-2-trifluoromethvI-7-(2.4.6-trimethyl-phenyl)-7H-imidazon,2- a1imidazol-3-ylmethvn-furan-2-ylmethyl-methyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.67 min., MS: [M+H] 451.

Example 315

r6-Chloro-2-trifluoromethvI-7-(2.4.6-trimethyl-phenyl)-7Jy-imidazon,2- a1imidazol-3-ylmethyll-(3.4-dichloro-benzyI)-ethyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.14 min., MS: [M+H]

543.

5-(2-BenzvI-pyrrolidin-l-yImethyl)-2-chloro-6-trifluoromethyl-l-(2,4,6- trimethyl-phenyl)- H^"-imidazo[l,2-a1imidazole, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = L80 min., MS: [M+H] 501.

2-Chloro-5-(3-phenyl-pyrrolidin-l-yImethyl)-6-trifluoromethyl-l-(2,4,6- trimethyl-phenyl)-lfi^"-imidazori,2-a1imidazole, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.78 min., MS: [M+H] 487. Example 318

6-Chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7g-imidazoπ,2- a1imidazol-3-ylmethvn-cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.38 min., MS: [M+H] =

543.

Example 319

r6-ChIoro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7g-imidazori,2- alimidazol-3-ylmethvn-cvcIopropyImethyl-ethyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: t = 1.64 min., MS: [M+H] 439. Example 320

r6-Chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl -7H-imidazon,2- a1imidazol-3-ylmethyn-cyclobtttylmethyl-(2,2,2-triflnoro-ethyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.40 min., MS: [M+H] = 507.

Example 321

r6-ChIoro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7g-imidazori,2- a1imidazol-3-ylmethyn-propyI-(3,3,3-trifluoro-propyl)-amine. scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.02 min., MS: [M+H] = 495.

r6-ChIoro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7fl^r-imidazon.2- a1imidazol-3-yImethvn-propyl-(2,2,2-trifluoro-ethyl)-amine. scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.29 min., MS: [M+H] 481.

Example 323

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7g-imidazori.2- a1imidazol-3-ylmethvn-(2,2,3,3.3-pentafluoro-propyl)-propyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.38 min., MS: [M+H] = 531. Example 324

r6-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7g-imidazori,2- a1imidazol-3-ylmethyn-phenethyl-(2.2,2-trifluoro-ethyl)-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 2.32 min., MS: [M+H] = 543.

Example 325

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7fl^r-imidazori,2- alimidazol-3-ylmethvn-phenethyI-propyI-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1-85 min., MS: [M+H] 503. Example 326

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazon.2- alimidazoI-3-vImethyn-ethyl-phenethyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1-79 min., MS: [M+H] 489.

Example 327

Benzyl-r6-chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7H-imidazoπ,2- a1imidazol-3-ylmethyn-(3,3,3-trifluoro-propyl)-amine. scheme 6: (DD)

Prepared as described for the example above. LC/MS: t_R = 2.34 min., MS: [M+H] = 543. Example 328

r6-ChIoro-2-trifluoromethvI-7-(2.4.6-trimethyl-phenyl)-7Jy-imidazon.2- a1imidazol-3-ylmethvn-(2-cyclopropyl-ethyl)-propyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.76 min., MS: [M+H] 467.

Example 329

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazoπ.2- a1imidazol-3-ylmethvn-(2-cvclopropyl-ethyl)-ethyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.71 min., MS: [M+H] 453.

- 0 -

Example 330

r6-Chloro-2-trifluoromethyl-7-(2.4«6-trimethvI-phenyl)-7fl^r-imidazon,2- a]imidazoI-3-ylmethyn-(2-cyclopropyl-ethyl)-(3,3.3-trifluoro-propyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.15 min., MS: [M+H] 521.

Example 331

r6-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7jy-imidazon.2- a]imidazol-3-ylmethyll-(2-cyclopropyl-ethyl)-(2,2.2-trifluoro-ethyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.01 min., MS: [M+H] 507. Example 332

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7g-imidazoπ,2- a]imidazoI-3-ylmethvn-(4-fluoro-benzyl)-(2,2,2-trifluoro-ethyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.33 min., MS: [M+H] =

547.

Example 333

-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7i^[j^r-imidazori.2- alimidazol-3-ylmethyll-(4-fluoro-benzyl)-(3,3,3-trifluoro-propyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.33 min., MS: [M+H] = 561.

r6-ChIoro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7g-imidazon.2- a1imidazol-3-ylmethvn-(4-fluoro-benzyl)-propyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.91 min., MS: [M+H] 507.

Example 335

r6-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7H-imidazon,2- alimidazol-3-ylmethvn-cyclobutylmethyl-propyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1-75 min., MS: [M+H] 467.

(4-Chloro-benzyl)-r6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7fif- imidazori,2-a1imidazol-3-ylmethyn-(3,3,3-trifluoro-propyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.42 min., MS: [M+H] = 577.

(4-Chloro-benzyl)-r6-chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7g- imidazori.2-a1imidazol-3-ylmethyn-propyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.05 min., MS: [M+H] -- 523. Example 338

Benzyl-r6-chloro-2-trifluoromethyl-7-(2,4.6-trimethyl-phenyl)-7g-imidazori,2- alimidazol-3-ylmethyn-propyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = L86 min., MS: [M+H] = 489.

Example 339

Allyl-r6-chIoro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7J^cf-imidazori,2- alimidazol-3-ylmethvn-propyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: t_R = 1.67 min., MS: [M+H] 539.

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7F-imidazori,2- a1imidazol-3-ylmethyl1-(3-fluoro-benzyl)-propyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC MS: to = 1.99 min., MS: [M+H] 507.

Example 341

r6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazori,2- alimidazol-3-ylmethyn-cycIobutvImethyl-ethyl-amine. scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = L72 min., MS: [M+H]

453. Example 342

r6-Chloro-2-trifluoromethyl-7-(2.4,6-trimethyl-phenyl)-7g-imidazori,2- a]imidazol-3-ylmethyll-(2-methoχy-ethyl)-propyl-amine, scheme 6: (DD) Prepared as described for the example above. LC/MS: to = 1.68 min., MS: [M+H]

457.

Example 343

r6-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7^r-imidazori.2- a1imidazoI-3-ylmethvn-(3-fluoro-benzyl)-(3,3,3-trifluoro-propyl)-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 2.32 min., MS: [M+H] = 561. Example 344

r6-Chloro-2-trifluoromethyl-7-(2.4.6-trimethyl-phenyl)-7g-imidazoπ.2- alimidazoI-3-ylmethyn-dipropyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = L68 min., MS: [M+H] 441.

Example 345

DialIyl-r6-chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7 r-imidazori,2- alimidazol-3-ylmethyll-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: to = 1.70 min., MS: [M+H] =

437.

Butyl-r6-chloro-2-trifluoromethyl-7-(2.4,6-trimethyl-phenyl)-7H-imidazoπ.2- alimidazol-3-ylmethvH-ethyl-amine, scheme 6: (DD)

Prepared as described for the example above. LC/MS: t_R = 1.71 min., MS: [M+H] = 441.

Example 347

3-(2-Benzyl-pyrrolidin-l-ylmethyl)-2-trifluoromethyl-8-(2,4,6-trimethyl- phenyI)-5,6,7,8-tetrahvdro-imidazori,2-a1pyrimidine. scheme 7: (KK) LC/MS: to = 1.7 min., MS: [M+H] = 483.

The following amine hydrochloride salts are intermediates that were used in many of the above examples:

Intermediate 118 - /o-

2-Cvclopropylethylamine hydrochloride

A IM solution of borane in tetrahydrofuran (250 mL„ 2 equiv.) that had been cooled to 0°C was added to cyclopropylacetonitrile (10.00 g, 123.3 mmoles) at 0°C under

nitrogen. The stirred mixture was heated at reflux for 12 hours, cooled to 0°C, and then carefully quenched with methanol (50 mL). The mixture was heated at reflux for 2 hours and then, upon re-cooling to 0°C, treated with a solution of t- butylpyrocarbonate (37.67 g, 1.4 equiv.) in methylene chloride (25 mL). The resulting mixture was stirred at room temperature overnight and then evaporated, the residue was partitioned between ethyl acetate and water. The organic was washed with water, brine, dried over magnesium sulfate, and evaporated to give the crude Boc-protected amine. This was dissolved in methylene chloride (25 mL) and treated with 4M hydrogen chloride in dioxane (77 mL, 2.5 equiv.). The mixture was stirred at room temperature overnight and then evaporated. The resulting white solid was triturated with ether and the product was collected by filtration, washed with ether, and dried in vacuo (12.72 g, 85%). 1H-NMR δ (CDC1₃) 0.14 (m, 2H), 0.52 (m, 2H), 0.75 (m, IH), 1.66 (q, 2H), 3.09 (m, 2H), 8.27 (br, 3H).

Intermediate 119

3.3,3-Trifluoroacetic acid N-hydroxysuccinimide active ester, scheme 8: (MM) A stirred solution of 3,3,3-trifluoroacetic acid (9.7 mL, 110 mmoles) and N- hydroxysuccinimide (13.92 g, 1.1 equiv.) in methylene chloride (100 mL) at 0°C was treated with EDC hydrochloride (21.08 g, 1 equiv.). The mixture was allowed to warm to room temperature. After stirring overnight, the solvent was evaporated and the residue partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over magnesium sulfate, and evaporated to give the crude active ester which was used without further purification (22.78 g, 92%). 1H-NMR δ

(CDC ) 2.86 (s, 4H), 3.51 (q, 2H).

Intermediate 120

Cyclopropylmethyl-3,3,3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

A stirred solution of 3,3,3-trifluoroacetic acid N-hydroxysuccinimide active ester (12.98 g, 57.65 mmoles) in methylene chloride (80 mL) at 0°C was treated with cyclopropylmethylamine (5.0 mL, 1 equiv.). The mixture was stirred at room temperature for 14 hours and then evaporated. The residue was partitioned between ethyl acetate and water. The organic phase was washed with water, brine, dried over magnesium sulfate, and evaporated to give the crude amide. This was dried under high vacuum for several hours and then, under a nitrogen atmosphere at 0°C, it was carefully treated with a IM solution of borane in tetrahydrofuran (173 mL, 3 equiv.). The mixture was heated at reflux for 14 hours and then re-cooled to 0°C. Methanol (50 mL) was added very carefully to avoid excess foaming, and the mixture was heated at reflux for 5 hours. Upon re-cooling to 0°C, a solution of t- butylpyrocarbonate (17.62 g, 1.4 equiv.) in methylene chloride (25 mL) was added. The resulting mixture was stirred at room temperature overnight and then evaporated. the residue was partitioned between ethyl acetate and water. The organic was washed with water, brine, dried over magnesium sulfate, and evaporated to give the crude Boc-protected amine. This was dissolved in methylene chloride (25 mL) and treated with 4M hydrogen chloride in dioxane (36 mL, 2.5 equiv.).. The mixture was stirred at room temperature overnight and then evaporated. The resulting white solid was triturated with ether and the product was collected by filtration, washed with ether,

and dried in vacuo (10.10 g, 86%). 1H-NMR δ (D₂O) 0.36 (m, 2H), 0.67 (m, 2H),

1.07 (m, IH), 2.72 (m, 2H), 2.99 (d, 2H), 3.89 (t, 2H).

Similarly prepared: Intermediate 121 2-Cvclopropylethyl-3,3.3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.14 (m, 2H), 0.52 (m, 2H), 0.74 (m, IH), 1.61 (m, 2H), 2.73 (m,

2H), 3.20 (t, 2H), 3.38 (t, 2H).

Intermediate 122 n-Propyl-3,3,3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.98 (t, 3H), 1.71 (q, 2H), 2.72 (m, 2H), 3.06 (t, 2H), 3.36 (t, 2H).

Intermediate 123

Benzyl-3,3.3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 2.73 (m, 2H), 3.40 (t, 2H), 4.31 (s, 2H), 7.51 (brs, 5H).

Intermediate 124 p-Fluoro-benzyl-3,3,3-trifluoropropyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 2.73 (m, 2H), 3.38 (t, 2H), 4.28 (s, 2H), 7.23 (ABq, 2H), 7.51

(ABq, 2H). Intermediate 125 p-Chloro-benzyl-3,3,3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 2.72 (m, 2H), 3.39 (t, 2H), 4.29 (s, 2H), 7.49 (q, 4H).

Intermediate 126 m-Fluoro-benzyl-3,3,3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 2.73 (m, 2H), 3.41 (t, 2H), 4.39 (s, 2H), 7.30 (m, 3H), 7.66 (m, IH).

Intermediate 127

2-PhenylethyI-3.3,3-trifluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 2.73 (m, 2H), 3.07 (t, 2H), 3.40 (m, 4H), 7.42 (m, 5H).

Intermediate 128 Benzyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

A stirred solution of benzylamine (5.0 mL, 45.77 mmoles) and triethylamine (6.4 mL, 1 equiv.) in methylene chloride (50 mL) at 0°C was treated with trifluoroacetic anhydride (6.5 mL, 1 equiv.), dropwise over 10 minutes. After 2 hours, the solvents were evaporated and the residue partitioned between ethyl acetate and 2% phosphoric acid. The organic phase was washed with water and brine, dried over magnesium sulfate, and evaporated. The crude amide was cooled to 0°C under nitrogen and treated with ice-cold IM borane-tetrahydrofuran complex (137 mL, 3 equiv.). The reaction mixture was heated at reflux for 14 hours and then cooled to 0°C. Methanol (50 mL) was carefully added and, when bubbling had largely ceased, the mixture was heated at reflux for 5 hours. Upon cooling to room temperature, the stirred mixture was treated with a solution of t-butylpyrocarbonate (14.00 g, 1.4 equiv.) in methylene chloride (25 mL). After continued stirring overnight at room temperature, the mixture was evaporated and the residue partitioned between ethyl acetate and water. The organic phase was washed with more water and brine, dried over magnesium sulfate, and evaporated. The residue in methylene chloride (25 mL) was treated with 4M hydrogen chloride in dioxane (69 mL, 1.5 equiv.) and the reaction was stirred at room temperature overnight. Evaporation gave a semi-solid that was triturated with ether. The resulting white solid product was collected by filtration, washed with ether, and dried in vacuo (9.28 g, 90%). 1H-NMR δ (D₂O) 3.97 (q, 2H), 4.07 (s, 2H), 7.52 (s, 5H).

Similarly prepared: Intermediate 129 Cvclopropylmethyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.39 (m, 2H), 0.72 (q, 2H), 1.08 (m, IH), 3.11 (d, 2H), 4.00 (q, 2H).

Intermediate 130 Cyclobutylmethyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 1.75-2.02 (m, 4H), 2.12 (m, 2H), 2.71 (m, IH), 3.24 (d, 2H), 3.93

(q, 2H). - oo-

Intermediate 131

2-Cyclopropylethyl-2,2.2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.14 (m, 2H), 0.53 (m, 2H), 0.76 (m, IH), 1.64 (q, 2H), 3.30 (t, 2H), 3.98 (q, 2H).

Intermediate 132 n-Propyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 1.00 (t, 3H), 1.76 (m, 2H), 3.17 (t, 2H), 3.97 (q, 2H).

Intermediate 133 p-Fluorobenzyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 3.98 (q, 2H), 4.40 (s, 2H), 7.24 (t, 2H), 7.53 (m, 2H).

Intermediate 134 m-Fluorobenzyl-2,2,2-trifluoroethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 3.97 (q, 2H), 4.39 (s, 2H), 7.30 (m, 3H), 7.66 (m, IH).

Intermediate 135 p-Chlorobenzyl-2.2.2-trifluoroethyl-amine hydrochloride. scheme 8: (OO) 1H-NMR δ (D₂O) 3.98 (q, 2H), 4.39 (s, 2H), 7.50 (m, 4H).

Intermediate 136

2-Phenylethyl-2.2.2-trifluoroethyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 3.10 (t, 2H), 3.49 (t, 2H), 4.00 (q, 2H), 7.41 (m, 5H). Intermediate 137

Cyclopropylmethyl-2,2,3.3,3-pentafluoropropyl-amine hydrochloride, scheme 8:

(OO) 1H-NMR δ (D₂O) 0.41 (m, 2H), 0.72 (m, 2H), 1.21 (m, IH), 3.14 (d, 2H), 4.06 (t,

2H).

Intermediate 138 n-Propyl-2,2,3,3,3-pentafluoropropyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 1.00 (t, 3H), 1.78 (m, 2H), 3.20 (t, 2H), 4.05 (t, 2H).

Intermediate 139 bis-Cyclopropylmethyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.35 (m, 2H), 0.68 (m, 2H), 1.07 (m, IH), 2.95 (d, 2H).

Intermediate 140

Cyclopropylmethyl-ethyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.34 (m, 2H), 0.67 (m, 2H), 1.04 (m, IH), 1.27 (t, 3H), 2.90 (d,

2H), 3.08 (q, 2H).

Intermediate 141

2-Cvclopropylethyl-ethyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.12 (m, 2H), 0.51 (m, 2H), 0.73 (m, IH), 1.28 (t, 3H), 1.60 (m,

2H), 3.12 (m, 4H). Intermediate 142

2-Cyclopropylethyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.13 (m, 2H), 0.51 (m, 2H), 0.72 (m, IH), 0.97 (t, 3H), 1.58 (q, 2H), 1.66 (m, 2H), 3.00 (t, 2H), 3.13 (t, 2H).

Intermediate 143

Cyclobutylmethyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.95 (t, 3H), 1.60-2.05 (m, 6H), 2.10 (m, 2H), 2.62 (m, IH), 2.96 (t, 2H), 3.06 (t, 2H).

Intermediate 144

Benzyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.96 (t, 3H), 1.71 (m, 2H), 3.04 (t, 2H), 4.23 (s, 2H), 7.50 (m, 5H).

Intermediate 145

3-Pyridylmethyl-propyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.99 (t, 3H), 1.73 (m, 2H), 3.13 (t, 2H), 4.51 (s, 2H), 8.11 (t, IH),

8.67 (d, IH), 8.87 (d, IH), 8.95 (s, IH).

Intermediate 146

2-Pyridylmethyl-propyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.97 (t, 3H), 1.71 (m, 2H), 3.14 (t, 2H), 4.50 (s, 2H), 7.81 (m, 2H),

8.30 (m, IH), 8.56 (d, IH). Intermediate 147

4-Pyridylmethyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 1.00 (t, 3H), 1.77 (m, 2H), 3.21 (t, 2H), 4.61 (s, 2H), 8.18 (d, 2H), 8.91 (d, 2H).

Intermediate 148 p-Fluorobenzyl-propyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.96 (t, 3H), 1.73 (m, 2H), 3.03 (t, 2H), 4.22 (s, 2H), 7.22 (t, 2H), 7.51 (m, 2H).

Intermediate 149 m-Fluorobenzyl-propyl-amine hydrochloride, scheme 8: (OO)

1H-NMR δ (D₂O) 0.98 (t, 3H), 1.73 (m, 2H), 3.14 (t, 2H), 4.39 (s, 2H), 7.30 (m, 3H), 7.65 (m, IH).

Intermediate 150 p- Chlorobenzyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.96 (t, 3H), 1.71 (m, 2H), 3.03 (t, 2H), 4.22 (s, 2H), 7.47 (q, 4H).

Intermediate 151

2-Phenylethyl-propyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 0.95 (t, 3H), 1.69 (m, 2H), 3.05 (m, 4H), 3.32 (t, 2H), 7.37 (m, 5H). Intermediate 152

2-Phenylethyl-ethyl-amine hydrochloride. scheme 8: (OO)

1H-NMR δ (D₂O) 1.26 (t, 3H), 3.11 (m, 4H), 3.32 (t, 2H), 7.41 (m, 5H).

Intermediate 153

Allyl-propylamine hydrochloride, scheme 8: (OO)

A stirred solution of allylamine (10.0 mL, 133.3 mmoles) in methylene chloride (80 mL) at 0°C was treated with propionic anhydride (8.54 mL, 0.5 equi.v), dropwise over 10 minutes. After 2 hours, the solvents were evaporated and the residue partitioned between ethyl acetate and 2% phosphoric acid. The organic phase was washed with brine, dried over magnesium sulfate, and evaporated. The crude amide in toluene (10 mL) was cooled to 0°C under nitrogen and treated with a 3.33M solution of Red-Al in toluene (7.1 mL, 2.5 equiv.). After stirring at room temperature for 14 hours, the mixture was cooled to 0°C and carefully quenched with acetone (12 mL). The reaction was allowed to warm to room temperature and then was treated with methanol (3 mL) and, after a further 1 hour at room temperature, a solution of t- butylpyrocarbonate (2.87 g, 1.4 equiv.) in methylene chloride (5 mL). After 14 hours at room temperature, the solvents were evaporated and the residue partitioned between ethyl acetate and 10% aqueous citric acid. The organic phase was washed with more water and brine, dried over magnesium sulfate, and evaporated. The residue in methylene chloride (5 mL) was treated with 4M hydrogen chloride in dioxane (6 mL, 2.5 equiv.) and the reaction was stirred at room temperature overnight. Evaporation gave a semi-solid that was triturated with ether, the resulting - o-

white solid product was collected by filtration, washed with ether, and dried in vacuo

(0.760 g, 60%). 1H-NMR δ (D₂O) 0.97 (t, 3H), 1.70 (m, 2H), 3.01 (t, 2H), 3.66 (d,

2H), 5.50 (t, 2H), 5.91 (m, IH).

REFERENCES

1. Kulagowski, J. J.; Moody, C. J.; Rees, C. W. Journal of Chemical Society Perkin Transaction I 1985, 2725 - 2733.

2. Zhou, J.; Oh, L. M.; Bakthavatchalay, R.; PCT WO 98/42706, pl6.

3. Scherz, M. W.; Fialeix, M.; Fischer, J. B.; Reddy, N. L.; Server, A. C; Sonders, M. S.; Tester, B. C; Weber, E.; Wong, S.; Keana, J. F. W. Journal ofMedcinal

Chemistry 1990, 33, 2421 - 2429.

4. Anisimova, V. A.; Kuzmenko, T. A.; Spasov, A. A.; Bocharova, I. A.; Orobinskaya, T. A. Pharmaceutical Chemistry Journal 1999, 33, 361 - 365.

5. Weijnen, J. G.; Koudijs, A.; Schellekens, G.; Engbersen, J. F.; Journal of Chemical Society Perkin Transaction II 1992, 829 - 834.

6. Cieplik, J.; Machon, Z.; Farmaco, 1995, 50, 131 - 136.

7. Basha, A.; Lipton, M.; Weinreb, S. M.; Tetrahedron Letters, 1977, 4171.

8. Bazant, V.; Capka, M.; Cerny, M.; Chvalousky, V.; Kochloefl, K.; Kraus, M.; Malek, J.; Tetrahedron Letters, 1968, 3303.

CRFi Receptor Binding Protocol

CRFi. receptor antagonists, by occupying the same receptors, blocks the accessibility of the receptors to CRF, a hypothalamic factor mediating body's responses to physiological and psychological stress. The following radioligand binding assay examines the ability of the antagonists to bind the CRFi receptors by - o -

assessing their ability to compete with binding of CRF to the receptors in cell membrane. Compounds of the present invention exemplified in examples 1-15 all showed Ki values less than 75 micromolar. See Table I.

Tissue culture and membrane preparation. IMR-32 cells were grown at 37°C in 5% CO₂ as a monolayer in medium consisting of MEM supplemented with 10% heat-

inactivated fetal bovine serum, 0.1 mM nonessential amino acids, 1 mM sodium pyruvate and 2 mM L-glutamine. Cells were transformed by exposure to 2.5 μM 5'- bromo-2'-deoxyuridine for 10 days. After transformation, cells were rinsed twice with phosphate-buffered saline, and incubated for 10-15 min. at 4°C in homogenization buffer consisting of 50 mM Tris (pH 7.2), 10 mM MgCl₂ and 2 mM EGTA. Cells were transferred from plates to polypropylene tubes (16 x 100 mm), homogenized and centrifuged at 32,000 x g for 15 min. Pellets were resuspended by homogenization in buffer and centrifuged at 32,000 x g for 15 min. Pellets were resuspended in homogenization buffer then stored at -80°C until needed.

Radioligand binding assays. Membranes (150 μg /well) were incubated with [¹²⁵I]- oCRF (100 pM) and increasing concentrations of test compound for 100 minutes at 25°C in a total volume of 200 μl. The assay buffer consisted of 50 mM Tris (pH 7.2), 10 mM MgCl₂, 0.5% BSA, 0.005% Triton X-100, 10 μg/mL aprotinin and 10 μg/mL leupeptin. Assays were stopped by addition of ice-cold wash buffer (50 mM Tris, pH 7.4 and 0.2% BSA). Filtration over glass fiber filters (Whatman GF/B) previously soaked in 50 mM Tris, pH 7.2 and 1% BSA was carried out using a Brandel cell harvester. Filters were washed with 10 mL of ice-cold wash buffer. Non-specific binding was defined with 10 μM oCRF. IC50 values for oCRF and test compounds were calculated by nonlinear regression using a one-site binding curve (GraphPad Prism).

Table I.

Key A < lOnM, B < 100 nM, C < 1,000 nM D < 10,000 nM

Claims (37)

What is claimed is:

1. A compound of Formula (I)

or a pharmaceutically acceptable salt or solvate thereof wherein

R¹ is H, Ci-βalkyl, -βhaloalkyl, -ealkoxy, -βthioalkyl, cyano, halo, C₃. ₇cycloalkyl, -C_halky lene-C₃. cycloalkyl, C₂.₆alkenyl or C₃_₆alkynyl;

R²is C(D)NR³R⁴, D'- D"(R³)(R⁴) or CH₂N R³R⁴ D' is CH₂ or a bond; D" is C, C-OH or CH wherein said C is attached to R³ by a single or double bond; said C is attached to R by a single or double bond; provided that

C is not attached to both R³ and R⁴ by double bonds; said CH is attached to R³ and R⁴ by single bonds; said C of C-OH is attached to R³ and R⁴ by single bonds; D is O or S;

R and R are each independently selected from the group consisting of H, Ci-βalkyl, Ci-_δhaloalkyl, - . alkylene-O-C₁.₄alkyl, -Ci-salkylene-Ci-βthioalkyl, -C₂_ 6alkylidene-(C₁.₄alkoxy)₂, C₃.₇cycloalkyl, -Ci-βalkylene- C₃.₇cycloalkyl, C₂-₆alkenyl, C₃.₆alkynyl, - -βalkylene-CN, -Ci- ₆alkylene-heterocyclo and -Cι-₆alkylene-aryl; wherein said aryl of said - -δalkylene-aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro, Cι.₄al yl and Cι_₃. alkoxy; or

R³ and R⁴ together with the nitrogen to which they are attached form a five or six-membered heterocycle, said heterocycle optionally containing one additional heteroatom selected from the group consisting of N, S and O; and said heterocycle optionally substituted with one or more groups selected from the group consisting of Ci-βalkyl, C^alkoxy, aryl, -Ci_ alkylene- aryl, pyridyl and halogen; wherein said aryl of said -Cι_₄alkylene- aryl is optionally substituted with one to three of the same or different substituents selected from the group consisting of fluoro, chloro, bromo, cyano, nitro and C^alkoxy;

X is C; Y is C;

A is

wherein

X¹ is N and is attached to X; Y¹ is N and is attached to Y;

G is

wherein Y² is N, CH, CH₂, C(O), C(S), CR⁵, CHR⁵ or CE¹ and is attached to Y¹;

J is CH, CH₂ , C(O), C(S), CR⁶, CHR⁶, a bond or CE²;

Z¹ is CH, CH₂, C(O), C(S), CR⁷, CHR⁷ or CE³ and is attached to Z; wherein

R , R and R are each independently selected from the group consisting of -CN, -Ci-₄. alk(en)ylene-CN, halo, Ci-βalkyl, C₂_ ₆alkenyl, C₃_₆alkynyl, Cι.₆haloalkyl, aryl, -C₁.₄alk(en)ylene-aryl, -Ci_ - alk(en)ylene-heterocyclo, heterocyclo, - amino, -Cι. alkylene- amino-C_Malkyl, aryl-amino, -amino-(C- ₁.₆alk(en)yl)₁.₂, -amino-aryl, -amino- heterocyclo, Cι-₆alkoxy, -O-aryl and - O-heterocyclo;

E¹ and E² together form moieties selected from the group consisting of C -alk(en)lyene, 5 N(CH)₃, CHN(CH)₂,N(CH)₂N,

N=NCH=N and NCHNCH; wherein said moieties are optionally substituted with halogen, -CN, - alkyl, C₃-C₆cycloalkyl, 10 substituted or unsubstituted phenyl, hydroxy, Cι-C₄alkoxy, SH, C C₄thioalkyl, NH₂, NH(C₁-C₄alkyl) orN(C₁- C₄alkyl)₂;

15 E² and E³ together form moieties selected from the group consisting of C₄-alk(en)lyene,

N(CH)₃, CHN(CH)₂,N(CH)₂N, N=NCH=N and NCHNCH; wherein said moieties are optionally 20 substituted with halogen, -CN,

C₁-C₄alkyl, C₃-C₆cycloalkyl, substituted or unsubstituted phenyl, hydroxy, C₁-C₄alkoxy, SH, C C₄thioalkyl, NH₂, 25 NH(C₁-C₄alkyl) or N(C

C₄alkyl)₂;

1 "λ

E and E together form moieties selected from the group consisting of C -alk(en)lyene, N(CH)₃, CHN(CH)₂, N(CH)₂N, 30 N=NCH=N and NCHNCH; wherein said moieties are optionally substituted with halogen, -CN, - alkyl, C₃-C₆cycloalkyl, substituted or unsubstituted phenyl, hydroxy, Cι-C₄alkoxy,

SH, Cι-C₄thioalkyl, NH₂, NH(Cι-C₄alkyl) or N(d- C₄alkyl)₂;

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of C₁.₄alkyl, d^alkoxy, Ci-βthioalkyl, C haloalkyl, halogen, N(C₁-C₄alkyl)₂ and CN; and provided that if Y² is N, then J is a bond and Z¹ is not CE³; if Y² is CE¹ and Z¹ is CE³, then J is a bond ; if Y²is not CE¹ and Z¹ is not CE³, then J is not CE²; if J is CE², then

Y² is CE¹ and Z¹ is not CE³, CR⁷ or CHR⁷; or Z¹ is CE² and Y² is not CE¹, CR⁵ or CHR⁵.

2. A compound according to claim 1 wherein V is phenyl or 3-pyridyl and is substituted with two to three of the same or different substitutents selected from the group consisting of ^alkyl, Cι_ alkoxy, d-ethioalkyl, C₁_₄haloalkyl, halogen, N(Cr C alkyl)₂ and CN; said substituents attached at the 2, 4 or 6-positions of said phenyl or said 3-pyridyl.

3. A compound according to claim 1 wherein V is 2-pyridyl and is substituted with two of the same or different substitutents selected from the group consisting of -βthioalkyl, C₁.₄haloalkyl, halogen, N(Ci-C₄alkyl)₂ and CN; said substituents attached at the 3 and 5-positions of said 2-pyridyl.

4. A compound according to claim 1 wherein R¹ is Ci-βalkyl or Ci-βhaloalkyl.

5. A compound according to claim 1 wherein R¹ is methyl or trifluoromethyl.

6. A compound according to claim 1 wherein R² is C(D)NR³R⁴ and D is O.

7. A compound according to claim 1 wherein R² is CH₂N R³R⁴.

8. A compound according to claim 1 wherein R² is D'- D"(R³)(R⁴), D is a bond and D" is C-OH.

9. A compound according to claim 1 wherein R² is D'- D"(R³)(R⁴), D is a bond and D" is C or CH.

10. A compound according to claim 1 wherein R³ and R⁴ are each independently selected from the group consisting of H, Ci-βalkyl, Ci_₆haloalkyl, - . βhydroxyalkyl, -Cι.₄alkylene-O-C₁_₄alkyl, -C₁-3alkylene-C1.6thioal.kyl, -C _ 6alkylidene-(C₁.₄alkoxy)₂, C₃.₇cycloalkyl, - -ealkylene-Cs^cycloalkyl, C₂. ₆alkenyl, C _₆alkynyl and -Q-βalkylene-CN.

11. A compound according to claim 1 wherein R and R together with the nitrogen to which they are attached form a five or six-membered heterocycle.

12. A compound according to claim 1 wherein V is 2, 4, 6-trimethylphenyl.

13. A compound according to claim 1 wherein V is 2,4-dichlorophenyl.

14. A compound according to claim 1 wherein R⁵, R⁶ and R⁷ are each independently selected from the group consisting of halogen, Ci-ealkyl, Ci-βhaloalkyl, benzyl, phenyl, Ci-salkyl-imidazolyl, Ci_₃alkyl-indolyl and .salkyl-pyridyl.

15. A compound according to claim 1 wherein Y² is CH₂, J is a bond and Z¹ is CH₂.

16. A compound according to claim 1 wherein Y² is CH, J is a bond and Z¹ is CH.

17. A compound according to claim 1 wherein Y² is CR⁵, J is a bond and Z¹ is CH wherein said R⁵ is halo.

18. A compound according to claim 1 wherein Y² is CH, J is a bond and Z¹ is CR⁷ wherein said R⁷ is halo.

19. A compound according to claim 1 wherein Y² is CH, J is a bond and Z¹ is CR⁷ wherein said R⁷ is halo, cyano or C^aUcyl.

20. A compound according to claim 1 wherein Y² is C(O), J is a bond and Z¹ is CH₂.

21. A compound according to claim 1 wherein Y² is CH₂ , J is a bond and Z¹ is C(O).

22. A compound according to claim 1 wherein Y² is CH₂, J is CH₂ and Z¹ is CH₂.

23. A compound according to claim 1 wherein R¹ is CN or CF₃ and Y² is CH₂, J is CH₂and Z¹ is CH₂.

24. A compound according to claim 1 wherein Y² is C(O), J is CH and Z¹ is CH.

25. A compound according to claim 1 wherein Y² is CH , J is CH and Z¹ is C(O).

26. A compound according to claim 1 wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form C -alk(en)lyene optionally substituted with halogen.

27. A compound according to claim 1 wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃ optionally substituted with halogen, methoxy, methyl or nitrile.

28. A compound according to claim 1 wherein R²is CH₂NR³R⁴, R³ is ethyl or propyl, R⁴ is -(CH₂)₂-phenyl, Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃ optionally substituted with halogen, methoxy, methyl or nitrile.

29. A compound according to claim 1 wherein Y² is CE¹, J is a bond , Z¹ is CE³ wherein E¹ and E³ together form N(CH)₃, CHN(CH)₂, N(CH)₂N, N=NCH=N or NCHNCH optionally substituted with halogen.

30. A compound or pharmaceutically acceptable salt of solvate thereof selected from the group consisting of Cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-[2- trifluoromethyl-8-(2,4,6-trimethyl-phenyl)-5,6,7,8-tetrahydro-imidazo[l,2- a]pyrimidin-3-ylmethyl]-amine; Cyclopropylmethyl-(2,2,2-trifluoro-ethyl)-[2- trifluoromethyl-8-(2,4,6-trimethylphenyl-8H-l,3a,8-triaza-cyclopenta[α]inden-3- ylmethyl]-amine; Ethyl-[2-methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8- tetraaza-cyclopenta[α]inden-3-ylmethyl]-phenethyl-amine; Cyclobutylmethyl-[2- methyl-8-(2,4,6-trimethyl-phenyl)-8H-l,3a,7,8-tetraaza-cyclopenta[ ]inden-3- ylmethyl]-propyl-amine; [8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-8Η- l,3a,7,8-tetraaza-cyclopenta[a]inden-3-ylmethyl]-phenethyl-propyl-amine; [8-(2- Chloro-4,6-dimethyl-phenyl)-2-methyl-8H-l,3a,7,8-tetraaza-cyclopenta[α]inden- 3-ylmethyl]-cyclobutylmethyl-propyl-amine; [8-(2-Chloro-4,6-dimethyl-phenyl)- 2-methyl-8H-l,3a,7,8-tetraaza-cyclopenta[a]inden-3-ylmethyl]-ethyl-phenethyl- amine; 8-(2-Chloro-4,6-dimethyl-phenyl)-2-methyl-3-(3-phenyl-pyrrolidin- 1 - ylmethyl)-8H-l,3a,7,8-tetraaza-cyclopenta[ ]indene; 6-Chloro-2-ethyl-7-(2,4- dichlorophenyl)-7H-imidazo[l,2-a]imidazole-3-carboxylic acid N,N- dipropylamide; 3-[(N,N-Dipropylamino)methyl]-6-chloro-2-ethyl-7-(2,4- diclorophenyl)-7H-imidazo[l,2-a]imidazole; 6-Chloro-2-ethyl-7-(2,4,6- trimethylphenyl)-7H-imidazo[l,2-a]imidazole-3-carboxylic acid N- cyclopropylmethyl-N-ethylamide; 3-[(N-Cyclopropylmethyl-N- ethylamino)methyl]-6-chloro-2-ethyl-7-(2,4,6-trimethylphenyl)-7H-imidazo[l,2- ajimidazole; 6-Chloro-2-trifluoromethyl-7-(2,4,6-trlmethyl-phenyl)-7H- imidazo[l,2-a]imidazol-3-ylmethyl]-cyclopropylmethyl-(2,2,2-trifluoro-ethyl)- amine; 6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclopropylmethyl-(2,2,3,3,3-pentafluoro-propyl)-amine;

[6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2- a]imidazol-3-ylmethyl]-cyclopropylmethyl-ethyl-amine; [6-Chloro-2- trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[l,2-a]imidazol-3- ylmethyl]-cyclobutylmethyl-(2,2,2-trifluoro-ethyl)-amine; [6-Chloro-2- 1xifluoromethyl-7-(2,4,6-trimethyl-ρhenyl)-7H-imidazo[l,2-a]imidazol-3- ylmethyl]-propyl-(3,3,3-trifluoro-propyl)-amine; [6-Chloro-2-trifluoromethyl-7- (2,4,6-trimethyl-phenyl)-7H-imidazo[l,2-a]imidazol-3-ylmethyl]-ethyl- phenethyl-amine; [6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H- imidazo[l,2-a]imidazol-3-ylmethyl]-(2-cyclopropyl-ethyl)-(3,3,3-trifluoro- propyl)-amine; and [6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H- imidazo[l,2-a]imidazol-3-ylmethyl]-(2-cyclopropyl-ethyl)-(2,2,2-trifluoro-ethyl)- amine.

31. A method of treating depression, anxiety, affective disorders, post-traumatic stress disorder, post-operative stress, headache, drug addiction, eating disorders and obesity, sudden death due to cardiac disorders, iritable bowel syndrome, hypertension, syndrome X, inflammatory disorders, stress-induced immune suppression, infertility, stress-induced insomnia and other sleep disorders, seizures, epilepsy, stroke and cerebral ischemia, traumatic brain injury, yet other disorders requiring neuroprotection, drug or alcohol withdrawal symptoms, other disorders including tachycardia, congestive heart failure, osteoporosis, premature birth, psychosocial dwarfism, ulcers, diarrhea and post-operative ileus comprising the administration of a pharmaceutical composition comprising a compound according to claim 1.

32. A compound of Formula (WHH)

wherein

R¹ is H, Cι.₆alkyl, Ci_₆haloalkyl, -βalkoxy, -βthioalkyl, cyano, halo, C₃.₇cycloalkyl, -C₁.₆alkylene-C₃_₇cycloalkyl, C₂_6alkenyl or C₃.₆alkynyl;

R⁸ is O-Ci.₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group; X is C;

Y is C;

X¹ is N;

Y¹ is N;

Y² is CH₂; J is CH₂ or a bond;

Z^s CHior C^ and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Ci.₄alkyl, -ethioalkyl, C₁_₄haloalkyl, halogen, N(C₁-C₄alkyl)₂ and CN.

33. A process for preparing a compound of Formula (WHH)

wherein

R¹ is H, C]_..₆alkyl, C^haloalkyl, -βalkoxy, Ci.6thioalkyl, cyano, halo, C₃.₇cycloalkyl, -C₁.₆alkylene-C₃. cycloalkyl, C₂_6alkenyl or C₃.₆alkynyl;

R⁸ is -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C; X¹ is N;

Y¹ is N;

Y² is CH₂;

J is CH₂ or a bond; Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of ^alkyl, C^alkoxy, Q-ethioalkyl, . .jhaloalkyl, halogen, N(Ci-C alkyl)₂ and CN;

comprising reacting a compound of Formula (UFF)

wherein

Z, Z¹, J and Y² are defined as for Formula (WHH); with a compound of Formula (UFF ')

wherein

R¹, R⁸ , X, Y, X¹ and Y¹ are defined as for Formula (WHH); in the presence of a suitable base and polar aprotic solvent to yield a compound of Formula (VGG)

wherein R¹, R° , X, Y, X¹, Y\ Y J, Z¹ and Z are defined as for Formula

(WHH);

and reacting said compound of Formula (VGG) with a high-boiling point polar aprotic solvent and a suitable silver salt under suitably high temperature.

34. A compound of Formula (Z')

wherein R¹ is H, Ci_₆alkyl, Ci.₆haloalkyl, -όal oxy, Ci-βthioalkyl, cyano, halo, C₃. cycloalkyl, -C₁_₆alkylene-C₃.₇cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl;

R⁸ is O-d. alkyl, -N(CH₃)(OCH₃) or other suitable leaving group; X is C;

Y is C;

X¹ is N;

Y¹ is N;

Y² is CHor CR⁵; R⁵ is selected from the group consisting of -CN, -Ci_₄. alk(en)ylene-CN, halo, -βalkyl, C₂_₆alkenyl, C₃.

₆alkynyl, Ci-ehaloalkyl, aryl, -Cι_₄alk(en)ylene-aryl, -

Cι-₄alk(en)ylene-heterocyclo, heterocyclo, -Ci. alk(en)ylene- amino, -C₁-₄alkylene-amino-C₁_₄alkyl, aryl-amino, -amino-(C₁.₆alk(en)yl)₁-₂, -amino-aryl, - amino-heterocyclo, Cι.₆alkoxy, -O-aryl and -O- heterocyclo;

Z¹ is C(O); and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Ci_₄aιkyl, C^alkoxy, Ci-ethioalkyl, Cι_ ₄haloalkyl, halogen, N(C!-C₄alkyl)₂ and CN.

35. A process for preparing a compound of Formula (Z')

wherein

R¹ is H, Ci-ealkyl, Ci-βhaloalkyl, Ci-βalkoxy, Ci-βthioalkyl, cyano, halo, C₃.₇cycloalkyl, -Ci-₆alkylene-C₃.₇cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl;

R⁸ is O-Ci. alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C;

X¹ is N; Y¹ is N;

Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -Ci- . alk(en)ylene-CN, halo, -ealkyl, C₂.₆alkenyl, C₃. ealkynyl, Ci-ehaloalkyl, aryl, -Ci.₄alk(en)ylene-aryl, - C₁.₄alk(en)ylene-heterocyclo, heterocyclo, - .

₄alk(en)ylene- amino, -Cι-₄alkylene-amino-Cι_₄alkyl, aryl-amino, -amino-(Cι-6alk(en)yl)ι_₂, -amino-aryl, - amino-heterocyclo, Ci.₆alkoxy, -O-aryl and -O- heterocyclo; Z¹ is C(O); and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Ci- alkyl, d.₄alkoxy, Ci-βthioalkyl, . haloalkyl, halogen, N(Cι-C alkyl)₂ and CN;

comprising reacting a compound of Formula (X')

HZ, .Y:

-M M, ^<x' wherein Z, Z¹ and Y² are defined as for Formula (Z');

with a compound of Formula (UFF ')

wherein

R¹, R⁸ , X, Y, X¹ and Y¹ are defined as for Formula (Z'); in the presence of a suitable base and polar aprotic solvent to yield a compound of Formula (Y')

wherein

R¹, R⁸ , X, Y, X¹, Y¹, Y², Z¹ and Z are defined as for Formula (Z'); and reacting said compound of Formula (Y') with a high-boiling point polar aprotic solvent and a suitable silver salt under suitably high temperature.

36. A compound of Formula (AA')

wherein

R¹ is H, Ci.₆alkyl, Ci.₆haloalkyl, Ci-βalkoxy, Ci-ethioalkyl, cyano, halo, C₃. cycloalkyl, -Cι-₆alkylene-C₃. cycloalkyl, C₂_₆alkenyl or C₃.₆alkynyl; R⁸ is O-Cι_ alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C;

X¹ is N;

Y¹ is N; Y is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -Ci_₄_ alk(en)ylene-CN, halo, Cι_₆alkyl, C₂_₆alkenyl, C₃. βalkynyl, d-βhaloatkyl, aryl, -Ci.₄alk(en)ylene-aryl, - Ci.₄alk(en)ylene-heterocyclo, heterocyclo, -Cι_ ₄alk(en)ylene- amino, -Cι-₄alkylene-amino-Cι_₄alkyl, aryl-amino, -amino-(Cι-6alk(en)yl)ι- , -amino-aryl, - amino-heterocyclo, Ci-βalkoxy, -O-aryl and -O- heterocyclo;

Z¹ is CR⁷; wherein R⁷ is chloro or bromo; and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_ alkyl, Cι. alkoxy, Ci.₆thioalkyl, Q. haloalkyl, halogen, N(Cι-C₄alkyl)₂ and CN.

37. A process for preparing a compound of Formula (AA')

wherein

R¹ is H, Ci_₆alkyl, Ci_₆haloalkyl, Ci-βalkoxy, Ci_₆thioalkyl, cyano, halo, C₃.₇cycloalkyl, -Ci.₆alkylene-C₃.₇cycloalkyl, C₂.₆alkenyl or C₃.₆alkynyl;

R⁸ is O-Ci.₄alkyl, -N(CH₃)(OCH₃) or other suitable leaving group;

X is C;

Y is C; X¹ is N;

Y¹ is N;

Y² is CHor CR⁵;

R⁵ is selected from the group consisting of -CN, -Ci_₄. alk(en)ylene-CN, halo, Cι_ealkyl, C₂.₆alkenyl, C₃. ₆alkynyl, Ci-βhaloalkyl, aryl, -Ci_₄alk(en)ylene-aryl, -

Ci.₄alk(en)ylene-heterocyclo, heterocyclo, -Ci- ₄alk(en)ylene- amino, -Ci-₄alkylene-amino-Cι. alkyl, aryl-amino, -amino-(Cι-₆alk(en)yl)ι_₂, -amino-aryl, - amino-heterocyclo, Ci-βalkoxy, -O-aryl and -O- heterocyclo;

Z¹ is CR⁷; wherein R⁷ is chloro or bromo; and

Z is N-V, wherein V is phenyl, 2-pyridyl or 3-pyridyl substituted with two to three of the same or different substitutents selected from the group consisting of Cι_ alkyl, Cι_ alkoxy, Ci-ethioalkyl, Q.

.ihaloalkyl, halogen, N(Cι-C₄alkyl)₂ and CN; comprising reacting a compound of Formula (Z')

wherein

R¹, R⁸ , X, Y, X¹, Y¹, Y², and Z are defined as for Formula (AA'); and

Z¹ is C(O); with phosphoryl trichloride or phosphoryl tribromide, neat or with a suitable solvent and without a base or with a suitable base.