BLOOD-BRAIN BARRIER-PENETRANT DOPAMINE-B-HYDROXYLASE INHIBITORS FIELD OF THE INVENTION

This invention relates to: (a) compounds and pharmaceutically acceptable salts or solvates thereof that are useful as dopamines-hydroxylase inhibitors; (b) pharmaceutical compositions comprising such compounds, salts or solvates; (c) the use of such compounds, salts or solvates in therapy; (d) therapeutic methods of treatment using such compounds, salts or solvates; and (e) processes and intermediates useful for the synthesis of such compounds.

BACKGROUND OF THE INVENTION

The enzyme dopamines-hydroxylase (ϋβΗ), also known as dopamine β- monooxygenase, is expressed both in the periphery and the central nervous system (CNS). ϋβΗ catalyses the specific hydro xylation of dopamine (DA) to produce norepinephrine, also known as noradrenaline (NA). As such, inhibitors of ϋβΗ can inhibit the biosynthesis of NA, limiting its concentration and increasing DA levels.

Conventionally, interest in the development of inhibitors of ϋβΗ had centred on the hypothesis that inhibition of this enzyme may provide significant clinical improvements in patients suffering from cardiovascular disorders such as hypertension or chronic heart failure. The rationale for the use of ϋβΗ inhibitors is based on their capacity to inhibit the biosynthesis of NA, which is achieved via enzymatic hydro xylation of DA. Reduction of the biosynthesis of NA via inhibition of ϋβΗ can directly dampen sympathetic nerve function, the activation of which is the principal clinical manifestation of congestive heart failure (Parmley, W.W., Clin. Cardiol., 18: 440-445, 1995). Therefore, peripheral ϋβΗ inhibitors reduce sympathetic drive. ϋβΗ inhibitors may also find application in disorders of the CNS, including drug addiction, psychiatric disorders, reduced cognition or dementia. For example, cocaine primarily acts through inhibition of presynaptic dopamine (DA) transporters as well as the serotonin and norepinephrine transporters. Increased levels of synaptic DA and, thereby, DA receptor binding following cocaine administration is a key mechanism through which cocaine is reinforcing. Cocaine also modulates the endogenous opioid system, especially μ-opioid receptors (MOR), κ- opioid receptors (KOR), and preprodynorphin. Whereas stimulation of dopaminergic pathways may be sufficient to cause the reinforcing effects of cocaine, DA transporter gene deletion studies have shown that this pathway is not essential to the development of cocaine self- administration. Selective gene disruption of the MOR will, however, prevent the development of cocaine self-administration.

Disulfiram (Antabuse), which inhibits aldehyde dehydrogenase (ALDH) and has been used for more than 50 years in the treatment of alcoholism (Fuller, R.K. et al., J. Amer. Med. Assoc., 256: 1449-55, 1986), was found to reduce alcohol and cocaine intake in co-dependent patient population (Carroll, K.M. et al., Arch. Gen. Psychiatry, 61: 264-72, 2000; Carroll, K.M. et al., Addiction, 93: 713-27, 1998; Carroll, K.M. et al., J. Stud. Alcohol, 54: 199-208, 1993). Surprisingly, further studies revealed that disulfiram was at least as effective at treating cocaine addicts who do not consume alcohol, and may even be more effective (Carroll, K.M. et al., Arch. Gen. Psychiatry, 61: 264-72, 2004; George, T.P. et al., Biol Psychiatry, 47: 1080-6, 2000; Petrakis, I.L. et al., Addiction, 95: 219-28, 2000). Therefore, an ALDH- independent mechanism must be responsible for the ability of disulfiram to promote cocaine abstinence (Gaval-Cruz, M. et al., Mol. Interv., 9: 175-87, 2009; Weinshenker, D. et al., Neuropsychopharmacology, 32: 1433-51, 2007). Subsequently, Schroeder et al. tested the effects of disulfiram on cocaine and food self- administration behaviour and drug-primed reinstatement of cocaine seeking in rats (Schroeder, J. P. et al., Neuropsychopharmacology, 35: 2440-9, 2010). Their results suggest that disulfiram's efficacy in the treatment of cocaine addiction is associated with the inhibition of ϋβΗ and interference with the ability of environmental stimuli to trigger relapse (Schroeder, J.P. et al., Neuropsychopharmacology, 35: 2440-9, 2010).

Furthermore, the noradrenergic system plays a role in a number of cognitive domains, including working memory, attention, and memory consolidation (Coull, J.T. et al., Neurolmage, 10: 705-15, 1999; McGaugh, J.L. et al., Psychopharmacology, 202: 3-14, 2009; Sara, S.J., Neuroscience, 10: 211-23, 2009). However, noradrenergic system activity in excess may impair cognition. Animal studies have shown associations between excess noradrenergic activity and impairments in attention and working memory (Arnsten, A.F., Nat. Rev. Neurosci., 10: 410-22, 2009; Sara, S.J., Neuroscience, 10: 211-23, 2009). Other studies show decreased cognitive performance in people placed under stress conditions, suggesting excess noradrenergic activity affects human cognition as well (Campbell, H.L. et al., Pharmacol. Biochem. Behav., 88: 222-9, 2008; Hermans, E.J. et al., Science, 334: 1151-3, 2011). Given this association between cognitive performance and noradrenergic system activity, there remains the question of whether differences in basal levels of activity may relate to differences in cognitive performance and whether this relationship is also influenced by age. Noradrenergic system activity appears higher in older compared with younger adults, both peripherally and in the CNS (Featherstone, J. A. et al., J. Gerontol., 42, 271-6, 1987; Lawlor, B.A. et al., Biol. Psychiatry, 38: 185-8, 1995; Supiano, M.A. et al., Am. J. Physiol., 259: E422-31, 1990). Previously it has been demonstrated that the concentration of cerebrospinal fluid NA was higher in older compared with younger adults, but it is not known whether noradrenergic system age differences may be a factor in cognitive differences. Numerous studies have linked excess noradrenergic activity with cognitive impairment. As such, ϋβΗ inhibitors may find application in enhancing cognition, especially in those suffering from dementia, including frontotemporal dementia (FTD), Parkinson disease and Alzheimer disease (AD), or Mild Cognitive Impairment (MCI).

Several inhibitors of ϋβΗ have been thus far reported in the literature. Early first and second generation examples such as disulfiram (Goldstein, M. et al., Life Sci., 3:763, 1964) and diethyldithiocarbamate (Lippmann, W. et al., Biochem. Pharmacol., 18: 2507, 1969) or fusaric acid (Hidaka, H. Nature, 231, 1971) and aromatic or alkyl thioureas (Johnson, G.A. et al, J. Pharmacol. Exp. Ther., 171: 80, 1970) were found to be of low potency, exhibited poor selectivity for ϋβΗ and caused toxic side effects. The third generation of ϋβΗ inhibitors, however, were found to have much greater potency, such as, for example, nepicastat (RS -25560- 197, ICso 9nM) (Stanley, W.C., et al., Br. J. Pharmacol., 121: 1803-1809, 1997), which was developed to early clinical trials. Although it was initially developed for peripheral indications (hypertension and congestive heart failure), an important discovery was that nepicastat was found to cross the blood-brain barrier (BBB), and was thereby able to cause central as well as peripheral effects.

Nepicastat and its analogues are disclosed in W095/29165. Furthermore, WO 2004/033447 and WO 2008/136695 disclose ϋβΗ inhibitors having high potency and significantly reduced brain access, giving rise to potent and peripherally selective ϋβΗ inhibitors. However, these compounds would either not exhibit an effect in the CNS or would act primarily in the periphery, potentially resulting in unwanted secondary effects in the cardiovascular system or systemic tissues such as reduced sympathetic drive. A review of the mechanism, substrates and inhibitors of ϋβΗ, is given by Beliaev, A., et al. in Current Enzyme Inhibition, 5, 27-43, 2009.

Therefore, there remains an unfulfilled clinical requirement for a potent, non-toxic and CNS-penetrant/active inhibitor of ϋβΗ with suitable pharmacokinetic properties, which could be used for treatment of certain CNS disorders, including cocaine addiction, alcohol addiction, adjunct opioid addiction, cognition decline in FTD, cognition decline in MCI, cognition decline in AD, attention deficit-hyperactive disorder (ADHD), post-traumatic stress disorder (PTSD) and unipolar depression. A ϋβΗ inhibitor with similar or even greater potency than nepicastat and with beneficial CNS effects - including the ability to cross the BBB and exhibit a long residence time in the brain so as to provide a long duration of ϋβΗ inhibition in the CNS - would provide a significant improvement over all ϋβΗ inhibitor compounds thus far described in the prior art. Additionally, such compounds would preferably be orally bioavailable and easier and cheaper to synthesise.

During a SciFinder search, the following compounds were identified as commercially available. However, no reference was made to their disclosure in the scientific or patent literature.

Sejtosztodas Farmakologiaja (1979), 8(1), 79-100 discusses the antimicrobial effect of certain 1,2,4-triazoles and discloses the compound 6-(4-chlorophenyl)-2,5,6,7-tetrahydro-3H- pyrrolo[2,l-c]-l,2,4-triazole-3-thione which is not within the scope of the present invention. WO 2014/127350 Al discloses a genus of compounds that are modulators, such as positive allosteric modulators, of one or more subclasses of vasopressin receptors. The genus disclosed in this publication overlaps to a small extent with the genus of the present invention. However, multiple selections of non-preferred embodiments within the genus of WO 2014/127350 Al would be required to arrive at a compound of the present invention.

SUMMARY OF THE INVENTION

The present invention provides a compound of formula I, or a pharmaceutically acceptable salt or solvate thereof:

wherein:

Ri is hydrogen, Ci-C ₆ alkyl, partially or fully deuterated Ci-C ₆ alkyl, C3-C6 cycloalkyl, C2-C6 cyanoalkyl, Ci-C ₆ mercaptoalkyl or amino;

R ₂ is hydrogen or C1-C3 alkyl;

R ₃ is hydrogen or oxo;

or R ₂ and R3 combine to form a structure of formula la:

wherein:

X is CH ₂ , CR ₆ or N;

is a double bond when X is CR6 or N and is a single bond when X is CH ₂ ;

R ₄ is hydrogen or C1-C3 alkyl;

R5 is hydrogen or C1-C2 alkyl; or R4 and R5 combine, together with the carbon atom to which they are attached, to form a cyclopropyl ring wherein the CH ₂ moiety is optionally substituted with two deuterium (D) atoms;

R6 is hydrogen;

A is C5-C-7 cycloalkyl, furanyl, thiophenyl, methylthiophenyl or

wherein:

Xi is hydrogen, halo or methyl;

Xi' is hydrogen or halo;

X ₂ is hydrogen, halo or methyl;

X ₂ ' is hydrogen or halo;

X ₃ is hydrogen or fluoro;

n is 0 or 1, and when n is 0 a single or double bond joins the carbon atoms to which R3 and R ₄ are attached;

for use in therapy.

This invention is also directed to compounds of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, per se, provided that the following compounds are excluded:

This invention is also directed to compounds of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, for use in the treatment of conditions ameliorated by inhibition of ϋβΗ within the CNS.

This invention is also directed to compounds of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, in the manufacture of a medicament for treatment of conditions ameliorated by inhibition of ϋβΗ within the CNS.

This invention is also directed to a method for treating or preventing conditions ameliorated by inhibition of ϋβΗ within the CNS comprising administering a therapeutically effective amount of a compound of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, to a patient in need thereof.

This invention is also directed to a pharmaceutical composition comprising (i) a therapeutically effective amount of a compound of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof; and (ii) a pharmaceutically acceptable excipient. DETAILED DESCRIPTION OF THE EMBODIMENTS

A. Definitions

"Ci-C ₆ alkyl" means a monovalent unsubstituted saturated straight-chain or branched- chain hydrocarbon radical having from 1 to 6 carbon atoms. "C1-C2 alkyl", "C1-C3 alkyl", "C1-C4 alkyl" and "C1-C5 alkyl" have analogous meanings.

"partially or fully deuterated Ci-C ₆ alkyl" means a Ci-C ₆ alkyl wherein some or all of the hydrogen atoms, respectively, have been selectively replaced by deuterium.

"C3-C6 cycloalkyl" means a monovalent unsubstituted saturated cyclic hydrocarbon radical having from 3 to 6 carbon atoms. "C5-C-7 cycloalkyl" has analogous meaning.

"C2-C6 cyanoalkyl" means a monovalent cyano- substituted saturated straight-chain or branched-chain hydrocarbon radical having from 2 to 6 carbon atoms including that which forms the cyano group.

"Ci-C ₆ mercaptoalkyl" means a monovalent thiol-substituted saturated straight-chain or branched-chain hydrocarbon radical having from 1 to 6 carbon atoms.

"oxo" means an oxo radical, and may be depicted as =0.

"halo" means a fluorine (which may be depicted as -F), chlorine (which may be depicted as -CI), bromine (which may be depicted as -Br) or iodine (which may be depicted as -I) radical, "amino" means -NH ₂ .

"Pharmaceutically acceptable salt" means a salt such as those described in standard texts on salt formation, see for example: P. Stahl, et ah , Handbook of Pharmaceutical Salts: Properties, Selection and Use (VCHA/Wiley-VCH, 2002), or S.M. Berge, et al, "Pharmaceutical Salts" (1977) Journal of Pharmaceutical Sciences, 66, 1-19.

"Pharmaceutically acceptable solvate" means a molecular complex comprising the compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, water or ethanol. The term "hydrate" may be employed when said solvent is water. Pharmaceutically acceptable solvates include hydrates and other solvates wherein the solvent of crystallization may be isotopically substituted, e.g. D ₂ 0, d6-acetone, d ₆ -DMSO.

"Pharmaceutically acceptable excipient" means any ingredient of a pharmaceutical composition other than the compound(s) of the invention, or other known pharmacologically active components. The choice of excipient will to a large extent depend on factors such as the particular mode of administration, the effect of the excipient on solubility and stability, and the nature of the dosage form.

"Therapy", "treatment" and "treating" include both preventative and curative treatment of a condition, disease or disorder. It also includes slowing, interrupting, controlling or stopping the progression of a condition, disease or disorder. It also includes preventing, curing, slowing, interrupting, controlling or stopping the symptoms of a condition, disease or disorder.

Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practicing the claimed invention, from a study of the disclosure, and the appended claims. In the claims, the word "comprising" does not exclude other elements or steps, and the indefinite article "a" or "an" does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage.

B. Compounds

The invention provides a compound of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof:

with the proviso that the following compounds are excluded:

BO. Core structures

In some embodiments R ₂ is hydrogen or C1-C3 alkyl; and R3 is hydrogen or oxo to form a structure of formula II to 14:

Structure 12 is particularly preferred.

In some embodiments R ₂ and R3 of formula I combine to form a structure of formula la:

wherein:

X is CH ₂ , CR ₆ or N;

is a double bond when X is CR6 or N and is a single bond when X is CH ₂ .

In some of these embodiments is a double bond and X is N.

In some of these embodiments is a double bond and X is CR6. This embodiment is particularly preferred.

In some of these embodiments is a single bond and X is CH ₂ .

In some embodiments of formula I, n is 0 and a single bond joins the carbon atoms to which R ₃ and R ₄ are attached to form a structure of formula lb

In some embodiments of formula I, R ₄ and R5 combine, together with the carbon atom to which they are attached, to form a structure of formula Ic having a cyclopropyl ring wherein the CH ₂ moiety is optionally substituted with two deuterium atoms:

In some embodiments more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% of substituents R5 and A of compounds of formula I have the stereochemical configuration of formula Id

In some embodiments more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% of substituents Rs and A of compounds of formula I have the stereochemical configuration of formula Ie

Preferred embodiments of formula I include compounds of formula If, Ig and Ih. Formula Ih is particularly preferred.

(If) (Ig) (Ih) .

In some particularly preferred embodiments of formula If, Ig and Ih more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% have the stereochemical configuration of formulas Is, It and lu. Formula lu is particularly preferred.

(Is) (It) ( ^Ju )

Other preferred embodiments of formula I include compounds of formula Ii, Ij and Ik. Formula Ik is particularly preferred.

(Ii) (ij) (Ik)

In some particularly preferred embodiments of formula Ii, Ij and Ik more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% have the stereochemical configuration of formulas II, Im and In. Formula In is particularly preferred.

Bl. Substituent Ri

Ri is selected from the group consisting of hydrogen, Ci-Ce alkyl, partially or fully deuterated Ci-Ce alkyl, C3-C6 cycloalkyl, C2-C6 cyanoalkyl, Ci-Ce mercaptoalkyl and amino.

Ri is preferably selected from the group consisting of hydrogen and Ci-Ce alkyl.

In some embodiments Ri is hydrogen.

In some embodiments Ri is Ci-Ce alkyl.

In some embodiments Ri is partially deuterated Ci-Ce alkyl.

In some embodiments Ri is fully deuterated Ci-Ce alkyl.

In some embodiments Ri is C3-C6 cycloalkyl.

In some embodiments Ri is C2-C6 cyanoalkyl.

In some embodiments Ri is Ci-Ce mercaptoalkyl.

In some embodiments Ri is amino.

Ri is preferably selected from the group consisting of hydrogen, methyl, <¾-methyl, propyl, cyclopropyl, cyano methyl, mercaptoethyl and amino.

Ri is more preferably selected from the group consisting of hydrogen and methyl. In some embodiments Ri is preferably hydrogen.

In some embodiments Ri is preferably methyl.

In some embodiments Ri is preferably <¾-methyl.

In some embodiments Ri is preferably propyl.

In some embodiments Ri is preferably cyclopropyl.

In some embodiments Ri is preferably cyanomethyl.

In some embodiments Ri is preferably mercaptoethyl.

In some embodiments Ri is preferably amino.

Ri is most preferably hydrogen.

Substituent R ₂ (when not combined with R ₃ )

R ₂ is selected from the group consisting of hydrogen and C1-C3 alkyl.

In some embodiments R ₂ is hydrogen.

In some embodiments R ₂ is C1-C3 alkyl.

R ₂ is preferably selected from the group consisting of hydrogen and methyl.

In some embodiments R ₂ is preferably hydrogen.

In some embodiments R ₂ is preferably methyl.

R ₂ is most preferably hydrogen.

Substituent R ₃ (when not combined with R ₂ )

R ₃ is selected from the group consisting of hydrogen and oxo.

In some embodiments R ₃ is hydrogen.

In some embodiments R ₃ is oxo.

R ₃ is preferably hydrogen.

Substituent R ₄ (when not combined with R5)

R ₄ is selected from the group consisting of hydrogen and C1-C3 alkyl.

In some embodiments R ₄ is hydrogen.

In some embodiments R ₄ is C1-C3 alkyl.

R ₄ is preferably selected from the group consisting of hydrogen and methyl.

In some embodiments R ₄ is preferably hydrogen. In some embodiments R ₄ is preferably methyl.

R ₄ is most preferably hydrogen.

Substituent R5 (when not combined with R ₄ )

Rs is selected from the group consisting of hydrogen and C1-C2 alkyl.

In some embodiments R5 is hydrogen.

In some embodiments R5 is C1-C2 alkyl.

Rs is preferably selected from the group consisting of hydrogen and methyl.

In some embodiments R5 is preferably hydrogen.

In some embodiments R5 is preferably methyl.

Rs is most preferably hydrogen.

B6. Substituent R6

R6 is hydrogen.

B7. Substituent A

A is selected from the group consisting of C5-C-7 cycloalkyl, furanyl, thiophenyl, methylthiophenyl and

wherein:

Xi is hydrogen, halo or methyl;

Xi' is hydrogen or halo;

X ₂ is hydrogen, halo or methyl;

X ₂ ' is hydrogen or halo; and

X ₃ is hydrogen or fluoro.

Preferably A is

wherein Xi, Xi', X ₂ , X ₂ ' and X ₃ are as defined above.

More preferably A is

wherein:

Xi is hydrogen, fluoro, chloro or methyl;

Xi' is hydrogen, fluoro or chloro;

X ₂ is hydrogen, fluoro, chloro, bromo or methyl;

X ₂ ' is hydrogen, fluoro, chloro or bromo; and

X ₃ is hydrogen or fluoro.

In one preferred embodiment not all of Xi, Xi', X ₂ , X ₂ ' and X ₃ are hydrogen. Preferably A is selected from the group consisting of

 Most preferably A is selected from the group consisting of

B8. Specific embodiments of Compounds of Formula I

Various embodiments of substituents Ri, R ₂ , R ₃ , R4, Rs, R6, A, X, Xi, Xi', X ₂ , X ₂ ' and

X ₃ have been discussed in Bl to B7 above. These "substituent" embodiments can be combined with any of the "core structure" embodiments, discussed in BO above, to form further embodiments of compounds of formula I. All embodiments of compounds of formula I formed by combining the "substituent" embodiments and "core structure" embodiments, discussed above, are within the scope of Applicants' invention, and some preferred further embodiments of the compounds of formula I are provided below.

In some embodiments of formula I, structures of formula If, Ii, and II are highly preferred

(If) (Ii) (II)

Ri is selected from the group consisting of hydrogen and methyl;

R ₃ is selected from the group consisting of hydrogen and oxo;

R ₄ (if present) is selected from the group consisting of hydrogen and methyl;

R5 (if present) is selected from the group consisting of hydrogen and methyl; and

A is selected from the group consisting of

In some embodiments of formula I, structures of formula Ih, Ik, and In (in particular formula Ih) are highly preferred

(Ih) (Ik)

wherein:

Ri is selected from the group consisting of hydrogen and methyl;

R ₄ (if present) is selected from the group consisting of hydrogen and methyl;

R5 (if present) is selected from the group consisting of hydrogen and methyl;

R6 is hydrogen; and

A is selected from the group consisting of

In some embodiments of formula I, structures of formula Ih wherein more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% have the stereochemical configuration of formula Iu are even more highly preferred

(lu)

wherein:

Ri is selected from the group consisting of hydrogen and methyl;

R ₄ is selected from the group consisting of hydrogen and methyl;

R5 is selected from the group consisting of hydrogen and methyl;

R6 is hydrogen; and

A is selected from the group consisting of

In some embodiments of formula I, structures of formula Io, Ip and Iq (in particular formula are even more highly preferred

wherein:

A is selected from the group consisting of

In some embodiments of formula I, structures of formula Io wherein more than 50%, preferably more than 90%, more preferably more than 95% and even more preferably more than 99% have the stereochemical config even more highly preferred

(Iv)

wherein: A is selected from the group consisting of

The following compounds represent specific embodiments of the invention:

3-Phenylpyrrolidine- 1 -carbothioamide ;

3-(thiophen-2-yl)pyrrolidine- 1 -carbothioamide;

3-(4-Fluorophenyl)pyrrolidine-l-carbothioamide;

3 -phenylpiperidine- 1 -carbothioamide ;

3-(2,4-difluorophenyl)pyrrolidine-l-carbothioarnide;

(5)-3-phenylpyrrolidine- 1 -carbothioamide ;

3-methyl-3-phenylpyrrolidine- 1 -carbothioamide;

l-phenyl-3-azabicyclo[3.1.0]hexane-3-carbothioamide;

3 -cyclohexylpyrrolidine- 1 -carbothioamide ;

3-(5-methylthiophen-2-yl)pyrrolidine-l-carbothioamide;

( ?)-3-phenylpyrrolidine-l-carbothioamide;

3-(3,5-Difluorophenyl)pyrrolidine- 1-carbothioamide; 3 -o-tolylpyrrolidine- 1 -carbothioamide ;

3 -m-tolylpyrrolidine- 1 -carbothioamide ;

3-(thiophen-3-yl)pyrrolidine- l-carbothioamide;

3-(furan-3-yl)pyrrolidine- l-carbothioamide;

3-(furan-2-yl)pyrrolidine- 1 -carbothioamide;

3-(2,5-difluorophenyl)pyrrolidine- l-carbothioarriide;

3-(2,4,5-trifluorophenyl)pyrrolidine- l-carbothioamide;

3-(3,4-difluorophenyl)pyrrolidine- l-carbothioarriide;

(5)-3-(2,4,6-trifluorophenyl)pyrrolidine- l-carbothioarriide;

3-(2,3,4-trifluorophenyl)pyrrolidine- 1 -carbothioamide;

3-(2,3,5,6-Tetrafluorophenyl)pyrrolidine- l-carbothioamide;

3-(2,3,5-trifluorophenyl)pyrrolidine- l-carbothioamide;

(5)-3-(3 ,5-difluorophenyl)pyrrolidine- 1 -carbothioamide ;

( ?)-3-(3,5-difluorophenyl)pyrrolidine- l-carbothioamide;

(15,55)- l-(thiophen-2-yl)-3-azabicyclo[3 ]hexane-3-carbothioamide;

(1 ?,5 ?)- l-(thiophen-2-yl)-3-azabicyclo[3 ]hexane-3-carbothioamide;

3-(perfluorophenyl)pyrrolidine- l-carbothioamide;

(15,5 ?)- l-(3,5-Difluorophenyl)-N-methyl-3-azabicyclo[3 ]hexane-3-carbothioamide;

N-methyl-3-phenylpyrrolidine- l-carbothioamide;

3-(3,5-difluorophenyl)-N-methylpyrrolidine- 1-carbothioamide;

N-methyl-3-(2,3,5,6-tetrafluorophenyl)pyrrolidine- l-carbothioamide;

l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbot hioamide;

(1 ?,55)- l-(3,5-difluorophenyl)-3-azabicyclo[3 ]hexane-3-carbothioarriide;

(15,5 ?)- l-(3,5-difluorophenyl)-3-azabicyclo[3 ]hexane-3-carbothioarriide;

l-(2,4-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbot hioarriide;

l-(2,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbot hioarriide;

(15,5 ?)- l-(3,5-Difluorophenyl)-N-propyl-3-azabicyclo[3 ]hexane-3-carbothioamide;

l-(2,5-difluorophenyl)-N-(2-mercaptoethyl)-3-azabicyclo[3 ]hexane-3-carbothioamide;

(15,5 ?)- l-(3,5-difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3 ]hexane-3-carbothioamide; 4-(3,5-difluorophenyl)-N-methyl-2-oxopyrrolidine- 1-carbothioamide;

l-(3,5-Difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3 ]hexane-3-carbothioamide; 6-Phenyltetra ydro- lH-pyrrolo[l,2-c]imidazole-3(2H)-thione;

l-(3,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbot hiohydrazide;

1 -(3 ,5-Difluorophenyl)-N,N-dimethyl-3-azabicyclo [3.1.0]hexane-3 -carbothioamide;

N-(cyanomethyl)- l-(2,5-difluorophenyl)-3-azabicyclo[3 ]hexane-3-carbothioamide;

3-(3,5-Difluorophenyl)-N-methyl-2,3-di ydro- lH-pyrrole- 1-carbothioamide;

6-phenyl-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

6-(3,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

6-(2,4-Difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

6-(2,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole-3(2H)- thione;

(5a5,6a ?)-5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a5,6a ?)-5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5aS,6aR)-5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclop ropa[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5aR,6aS)-5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclop ropa[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

( ?)-6-(3,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

(5)-6-(3,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

(5a5,6a ?)-5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[2, l- c] [l,2,4]triazole-3(2H)-thione;

(5)-6-(2,3,5,6-tetrafluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

( ?)-6-(2,3,5,6-tetrafluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

(5a5,6a ?)-5a-(2,3,5-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa [3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a ?,6a5)-5a-(2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione; (5a5,6a ?)-5a-(2,3-difluorophenyl)-5,5a,6,6a-tetra ydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a ?,6a5)-5a-(2,3-difluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a5,6a ?)-5a-(2,3,6-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa [3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a ?,6a5)-5a-(2,3,6-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclop ropa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(2,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a5,6a ?)-5a-(3,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a5,6a ?)-5a-(2,4,5-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa [3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(3-chloro-5-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(2-chloro-5-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(3,5-difluorophenyl)-2-methyl-5,5a,6,6a-tetrahydrocycl opropa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5aS,6a ?)-2-cyclopropyl-5a-(3,5-difluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e;

6-cyclohexyl-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione;

(5)-6-(2,3,5-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[ l,2-c]imidazole-3-thione;

( ?)-6-(2,3,5-trifluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione;

(5)-6-(2,6-difluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione;

(5)-6-(3-chloro-2,6-difluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione; ( ?)-6-(3-chloro-2,6-difluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione;

( ?)-6-(2,6-difluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione; (5a5,6a ?)-5a-(3-chloro-2,6-difluorophenyl)-5,5(3,6,6i3-tetraliydroc yclopropa[3,4]pyrrolo[2,l- c][l,2,4]triazole-3(2H)-thione;

(5a5,6a ?)-5a-(2-chloro-6-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(3-chloro-2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocycl opropa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione-5,5-d2;

(5a5,6a ?)-5a-(3-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(5-bromo-2-fluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(3-bromo-5-fluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(5-chloro-2-fluorophenyl)-2-(methyl-<i3)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e;

5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetra ydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole- 3(2H)-thione-6,6,6a-<¾;

(5a ?,6a5)-5a-(3-chloro-2,6-difluorophenyl)-5,5a,6,6a-tetrahydro cyclopropa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a5)-5a-(3,5-difluorophenyl)-2,5,5a,6,6a,7-hexa ydro-3H-cyclopropa[<i]imidazo[l,5- a]pyridine-3-thione;

(6 ?,75)-7-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole- 3-thione;

(6 ?,7 ?)-7-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole- 3-thione;

(5a5,6a ?)-5a-(3,5-dichlorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole- 3(2H)-thione;

(5a ?,6a5)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocycl opropa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(6 ?)-6-(2,3,5,6-tetrafluorophenyl)tetra ydro-lH-pyrrolo[l,2-c]imidazole-3(2H)-thione; (5)-6-(2,3,6-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[ l,2-c]imidazole-3-thione;

( ?)-6-(2,3,6-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[l ,2-c]imidazole-3-thione;

( ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahydro -3H-pyrrolo[l,2-c]imidazole-3- thione;

(5a5,6a ?)-5a-(3-bromo-2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclo propa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione;

(5a5,6a ?)-5a-(5-chloro-2-fluorophenyl)-2-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e;

(5)-6-(3-bromo-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyr rolo[l,2-c]imidazole-3-thione; ( ?)-6-(3-bromo-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyrr olo[l,2-c]imidazole-3-thione; (5a5,6a ?)-5a-(3-bromo-2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclo propa[3,4]pyrrolo[2, l- c] [ 1 ,2,4]triazole-3(2H)-thione; and

(5a5,6a ?)-5a-(5-bromo-2-fluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[2, l- c] [l,2,4]triazole-3(2H)-thione .

C. Compositions

The compounds of the invention intended for pharmaceutical use may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs (or as any combination thereof). Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients. Accordingly, the present invention is also directed to a pharmaceutical composition comprising (i) a therapeutically effective amount of a compound of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof; and (ii) a pharmaceutically acceptable excipient.

Pharmaceutical compositions suitable for the delivery of compounds of the present invention and methods for their preparation will be readily apparent to those skilled in the art. Such compositions and methods for their preparation may be found, for example, in "Remington's Pharmaceutical Sciences", 19th Edition (Mack Publishing Company, 1995). D. Methods of Use

This invention is also directed to compounds of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, for use in therapy, in particular for the treatment of conditions ameliorated by inhibition of ϋβΗ within the CNS.

This invention is also directed to the use of compounds of formula I, as defined above, or a pharmaceutically acceptable salt or solvate thereof, in the manufacture of a medicament for treatment of conditions ameliorated by inhibition of ϋβΗ within the CNS.

This invention is also directed to a method for treating conditions ameliorated by inhibition of dopamine-beta-hydroxylase within the CNS comprising administering a therapeutically effective amount of a compound of formula I, as defined in claim 1, or a pharmaceutically acceptable salt or solvate thereof, to a patient in need thereof.

Conditions ameliorated by inhibition of ϋβΗ within the CNS can include, but are not limited to: cocaine addiction, alcohol addiction, adjunct opioid addiction, cognition decline in FTD, cognition decline in MCI, cognition decline in AD, ADHD, PTSD and unipolar depression.

E. General synthetic methodology

The methods used for the synthesis of the compounds of the invention are illustrated by the schemes below. The starting materials and reagents used in preparing these compounds are available from commercial suppliers or can be prepared by methods obvious to those skilled in the art. To make the schemes easier to read, the option to incorporate deuterium at certain positions is not shown. Specifically, deuterated products can be produced using specifically deuterated starting materials, including, but not limited to, those used in Examples 1-121.

Compounds of formula 12 can generally be synthesised by the methods outlined in Scheme 1. Scheme 1

Compounds of formula 14 can generally be synthesised by the method outlined in Scheme 2:

Compounds of formula la, where X = CH ₂ can generally be synthesised by the method outlined in Scheme 3:

Scheme 3

Compounds of formula la, where X = CR ₆ can generally be synthesised by the method outlined in Scheme 4:

Scheme 4

When R6 = H, the starting material in Scheme 4 can generally be synthesised by the method outlined in Scheme 5:

Scheme 5

The starting material for Scheme 5, when n = 0, can generally be synthesised by the method outlined in Scheme 6 as either enriched enantiomers or racemates:

Scheme 6

When R6 = H and R ₄ and Rs combine to form a cyclopropyl group, the starting material in Scheme 4 can generally be synthesised by the method outlined in Scheme 7:

Scheme 7

The starting material for Scheme 7 can generally be synthesised by the method outlined in Scheme 8: Scheme 8

Compounds of formula la, where X = N can generally be synthesised by the method outlined in Scheme 9:

Scheme 9

The starting material for Scheme 9, when n = 0 and R ₄ and R ₅ combine to form a cyclopropyl group, can generally be synthesised by the method outlined in Scheme 10:

Scheme 10

In turn, the starting material for Schemes 8 and 10 can generally be synthesised by the method outlined in Scheme 11 as either enriched enantiomers or racemates and including specific deuteration:

Scheme 11

©

In accordance with this synthetic methodology, the invention provides a process for the preparation of compounds of formulae 12 or la wherein is a double bond and X is

CR ₆

which comprises reacting a compound of formula 112 or Ila wherein n, R ₄ , Rs, R6 and A are as defined for formula I above

(Ila)

with a compound of formula R ¹ -N=C=S.

Compounds of formula 112 and Ila wherein n, Rt, Rs, R6 and A are as defined for formula I above are thus useful intermediates representing further embodiments of the present invention.

F. Examples

All compounds and intermediates were characterised by NMR. The spectra were recorded on a Bruker Avance III 600 MHz spectrometer with solvent used as internal standard. ¹³ C spectra were recorded at 150 MHz and ^l H spectra were recorded at 600 MHz. Data are reported in the following order: approximate chemical shift (ppm), number of protons, multiplicity (br, broad; d, doublet; m, multiplet; s, singlet; t, triplet) and coupling constant (Hz).

Room temperature in the following protocols means the temperature ranging from 20 °C to 25 °C.

Example 1; 3-Phenylpyrrolidine- 1-carbothioamide

Step 1: N-(3-phenylpyrrolidine-l-carbonothioyl)benz mide To a solution of ammonium thiocyanate (62 mg, 0.815 mmol) in acetone (2 mL) was added benzoyl chloride (0.087 mL, 0.747 mmol) at room temperature with stirring. After being stirred for 10 min. the resulting precipitate was filtered off and 3-phenylpyrrolidine (CAS#936-44-7) (100 mg, 0.679 mmol) was added to the filtrate in portions. The reaction mixture was stirred at ambient temperature for 20 h, and then evaporated to dryness. Chromatography (petroleum ether - ethyl acetate, 4: 1) gave N-(3-phenylpyrrolidine-l-carbonothioyl)benzamide as an off-white powder (0.067 g, 32% yield).

Step 2: 3-phenylpyrrolidine-l-carbothioamide

To a solution of N-(3-phenylpyrrolidine-l-carbonothioyl)benzamide (0.06 g, 0.193 mmol) in methanol (2 mL) was added 20% aq. sodium hydroxide (0.317 mL, 1.933 mmol) and the mixture was refluxed for 6 h. Thereupon, the reaction was diluted with water (4 mL) and then the organics were removed under vacuum to give the product as an oil that solidified on standing in the cold (5 °C). The crystals were collected, washed with water and dried to give 3- phenylpyrrolidine-l-carbothioamide as an off-white powder (0.018 g, 45% yield).

Ή NMR (DMSO-iM): 7.33 (2H, t, J = 7.3 Hz), 7.29 (2H, d, J = 7.2 Hz), 7.24 (1H, t, J = 7.2 Hz), 7.19 (2H, br s), 4.12 (0.5 H, m), 3.90 (0.5 H, m), 3.78 (0.5 H, m), 3.44-3.61 (2H, m), 3.26 (0.5 H, m), 2.34 (0.5 H, s br), 2.20 (0.5 H, s br), 2.11 (0.5 H, m), 1.97 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.5, 141.2, 141.1, 128.5, 127.1, 126.8, 126.7, 57.5, 53.9, 51.3, 47.5, 44, 42.4, 33,0, 31.9.

Example 2: 3-(thiophen-2-yl)p

3-(Thiophen-2-yl)pyrrolidine (CAS#125067-53-0) was converted to 3-(thiophen-2- yl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 1 and the product was isolated as an off-white powder. Ή NMR (DMSO-ίΜ): 7.39 (1 H, d, J = 4.4 Hz), 7.19 (2 H, br, s), 6.98 (1 H, dd, J = 5.0, 3.5 Hz), 6.96 (1 H, d, J = 2.9 Hz), 4.10 (0.5 H, br s), 3.86 (0.5 H, br s), 3.80 (1 H, br s), 3.66 (0.5 H, br s), 3.53 (1.5 H, m), 3.38 (0.5 H, m), 3.29 (0.5 H, br s), 2.39 (0.5 H, m), 2.26 (0.5 H, br s), 2.09 (0.5 H, br s), 1.95 (0.5 H, tar s).

1 ³ C NMR (DMSO-iM): 178.5, 144.7, 127, 124.1, 124.1, 124, 58.1, 54.6, 51, 47.2, 39.2, 37.9, 34.1, 33,0.

Example 3: 3- -Fluorophenyl)pyrrolidine- 1-carbothioamide

To a solution of Ι, Γ-thiocarbonyldiimidazole (0.570 g, 3.20 mmol) in tetrahydrofuran (6 mL) was added a solution of 3-(4-fluorophenyl)pyrrolidine (CAS#144620-11-1) (0.48 g, 2.91 mmol) in tetrahydrofuran (6.00 mL). The mixture was then stirred for 1 h at room temperature and for an additional 2 h at 55-60 °C. Thereupon, tetrahydrofuran was removed under vacuum and the residue was dissolved in methanol (12 mL). The thus obtained solution was treated with 25% aq. ammonia (3.26 mL, 43.6 mmol) and then the mixture was stirred at room temperature for 5 days. The reaction was diluted with 1M HCl, the resulting precipitate was collected, washed with a mixture of methanol-water (1: 1) and dried under vacuum at 50 °C to give 3-(4- fluorophenyl)pyrrolidine- 1-carbothioamide as a white powder (0.22 g, 34% yield).

Ή NMR (DMSO-iM): 7.33 (2H, m), 7.15 (2H, m), 6.70-7.60 (2 H, br s), 4.11 (0.5 H, m), 3.90 (0.5 H, m), 3.77 (0.5 H, m), 3.52 (1.5 H, m), 3.40 (1.5 H, m), 3.23 (0.5 H, m), 2.33 (0.5 H, br s), 2.18 (0.5 H, br s), 2.09 (0.5 H, m ), 1.96 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.4, 161.8, 160.2, 137.2, 129, 129, 115.3, 115.1, 57.5, 54, 51.3, 47.4, 43.3, 41.7, 33.1, 31.9. Example 4: 3-phenylpiperidine- 1-carbothioamide

3-Phenylpiperidine (CAS#3973-62-4) was converted to 3-phenylpiperidine-l-carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a white powder. Ή NMR (DMSO-iM): 7.38 (2 H, br s), 7.32 (2 H, t, J = 7.8 Hz), 7.29 (2 H, d, J = 7.8 Hz), 7.23 (1 H, mt, J = 7.1 Hz), 4.59 (2 H, m), 2.96 (2 H, m), 2.64 (1 H, m), 1.90 (1 H, m), 1.70 (2 H, m), 1.50 (1 H, m).

¹³ C NMR (DMSC M): 180.5, 143.3, 128.4, 127.1, 126.5, 53.7, 47.6, 42,0, 31.3, 25.0,

Example 5: 3-(2,4-difluorophenyl)pyrrolidine- 1-carbothioamide

3-(2,4-Difluorophenyl)pyrrolidine (CAS#1092108-80-9) was converted to 3-(2,4- difluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a beige powder.

Ή NMR (DMSO-iM): 7.39 (1H, m), 7.19 (1 H, ddd, J = 11.0, 9.2, 2.6 Hz), 7.09 (2H, br s), 7.07 (1H, ddt, J = 1.0, 2.6, 8.5 Hz), 3.34-4.24 (5H, m), 2.28 (1H, br s), 2.09 (1H, br s).

¹³ C NMR (DMSO- 6): 178.6, 178.5, 162, 161.9, 161.2, 160.4, 160.3, 159.6, 129.4, 129.2, 129, 129, 124.9, 124.1, 115.3, 115.1, 111.7, 111.5, 104.1, 103.9, 103.8, 56.1, 52.5, 50.9, 37.1, 35.5, 31.6, 30.4. Example 6: (5)-3-phenylpyrro (S)-3-phenylpyrrolidine (CAS#62624-46-8) was converted to (5)-3-phenylpyrrolidine-l- carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a beige powder.

Ή NMR (DMSO-iM): 7.33 (2H, t, J = 7.2 Hz), 7.29 (2H, d, J = 7.4 Hz), 7.24 (1H, t, J = 7.1 Hz), 7.21 (2H, br s), 4.12 (0.5 H, m), 3.90 (0.5 H, m), 3.78 (0.5 H, m), 3.44-3.61 (2H, m), 3.26 (0.5 H, m), 2.34 (0.5 H, s br), 2.20 (0.5 H, s br), 2.11 (0.5 H, m), 1.97 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.4, 141.2, 141.1, 128.5, 127.1, 126.7, 126.7, 57.5, 53.9, 51.3, 47.5, 44, 42.4, 33,0, 31.9.

Example 7: 3-methyl-3-phenylp

3-Methyl-3-phenylpyrrolidine (CAS#56606-73-6) was converted to 3-methyl-3- phenylpyrrolidine- 1 -carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a white solid.

Ή NMR (DMSO-iM): 6.80-7.60 (7 H, m), 3.89 and 3.82 (1 H, 2 br d, J = 11.4 Hz), 3.68 (1 H, m), 3.60 and 3.54 (1 H, 2 br d, J = 10.8 Hz), 3.45 (0.5 H, m), 2.27 (0.5 H, m), 2.21 (0.5 H, m), 2.10 (1 H, m).

¹³ C NMR (DMSO- 6): 178.9, 178.6, 146.8, 146.6, 128.4, 126.3, 126.2, 125.7, 125.5, 62.3, 58.9, 50.1, 46.4, 46.2, 44.5, 37.7, 36.2, 27.5, 27.1.

Example 8: l-phenyl-3-azabicyc e l-phenyl-3-azabicyclo[3.1.0]hexane (CAS#67644-21-7) was converted to l-phenyl-3- azabicyclo[3.1.0]hexane-3-carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 6.8-7.9 (2H, br s), 7.31 (2H, t, J = 7.6 Hz), 7.31 (3 H, m), 4.39 (0.5H, br s), 4.09 (0.5 H, br s), 3.95 (0.5 H, br s), 3.47-3.80 (2.5 H, m), 1.90-2.21 (1 H, m), 1.10 (1 H, br dd, J = 7.6, 5.0 Hz), 0.72 (1 H, t, J = 4.6 Hz).

¹³ C NMR (DMSO-iM): 179.9, 140.9, 128.4, 126.4, 126.2, 57.3, 54, 53.5, 50.2, 31.8, 30.2, 24.5, 23.6, 19.5.

Example 9: 3-cyclohexylpyrro

3-cyclohexylpyrrolidine (CAS#78813-85-1) was converted to 3-cyclohexylpyrrolidine- 1- carbothioamide by a similar procedure as described for Example 3 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.08 (2 H, br s), 3.87 (0.5 H, br t, J = 9 Hz), 3.81 (0.5 H, br t, J = 9.7 Hz), 3.51 (0.5 H, br t, J = 8.5 Hz), 3.43 (0.5 H, m), 3.32 (0.5 H, m), 3.18 (0.5H, m), 3.03 (0.5 H, t, J = 10.8 Hz), 2.86 (0.5 H, J = 10 Hz), 2.07 (0.5 H, m), 1.94 (1H, m), 1.82 (0.5 H, m), 1.57-1.77 (5.5H, m), 1.42 (0.5 H, m), 1.17 (4.0 H, m), 0.94 (2H, m).

¹³ C NMR (DMSC M): 178.2, 55.6, 51.9, 51.5, 47.7, 45.4, 43.6, 41.1, 40.8, 31.5, 31.4, 30.8, 30,0, 28.9, 25.6, 25.5.

Example 10: 3- -methylthiophen-2-yl)pyrrolidine- 1-carbothioamide

To a stirred solution of Ι, Γ-thiocarbonyldiimidazole (0.469 g, 2.63 mmol) in dry tetrahydrofuran (9 mL) was added a solution of 3-(5-methylthiophen-2-yl)pyrrolidine (CAS#1260863-70-4) (0.44 g, 2.63 mmol) in dry tetrahydrofuran (9 mL). The reaction was stirred for 1 h at room temperature and for an additional 2 h at 55-60 °C. After being cooled to room temperature, the organics were evaporated to dryness under vacuum and the residue was treated with 2 M ethanolic ammonia solution (7.89 mL, 15.78 mmol). The reaction was stirred for 16 h in a sealed vial at 70 °C. The mixture was then cooled again and quenched water (2 mL). The resulting crystals were collected, washed with a mixture of ethanol-water (1: 1) and dried under vacuum at 50 °C to give 3 -(5-methylthiophen-2-yl)pyrrolidine-l -carbothioamide as a white powder (0.3 g, 1.325 mmol, 50.4% yield).

Ή NMR (DMSO-iM): 6.84 (2 H, br d, J = 3.5 Hz), 6.71 (1 H, d, J = 3.2 Hz), 6.63 (1 H, m), 4.04 (0.5 H, br s), 3.83 (0.5 H, br s), 3.72 (1 H, m), 3.50 (2 H, m), 3.35 (0.5 H, m), 3.25 (0.5 H, m), 2.39 (3 H, m), 2.30 (0.5 H, m), 2.22 (0.5 H, br s), 2.04 (0.5 H, br s), 1.90 (0.5 H, br s).

¹³ C NMR (DMSO- 6): 178.6, 178.5, 142.3, 142.3, 137.3, 137.2, 125,0, 123.8, 58,0, 54.4, 51,0, 47.1, 39.4, 38,0, 34,0, 32.9, 15.0,

Example 11: ( ?)-3-phenylpyrro

( ?)-3-phenylpyrrolidine (CAS#61586- 46-7) was converted to ( ?)-3-phenylpyrrolidine-l- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder

Ή NMR (DMSO-iM): 7.33 (2H, t, J = 7.2 Hz), 7.29 (2H, d, J = 7.4 Hz), 7.24 (1H, t, J = 7.1 Hz), 7.21 (2H, br s), 4.12 (0.5 H, m), 3.90 (0.5 H, m), 3.78 (0.5 H, m), 3.44-3.61 (2H, m), 3.26 (0.5 H, m), 2.34 (0.5 H, s br), 2.20 (0.5 H, s br), 2.11 (0.5 H, m), 1.97 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.5, 141.2, 141.1, 128.5, 127.1, 126.8, 126.7, 57.5, 53.9, 51.3, 47.5, 44, 42.4, 33, 31.9.

Example 12: 3-(3,5-Difluorophenyl)pyrrolidine- 1 -carbothioamide

3-(3,5-Difluorophenyl)pyrrolidine (CAS#1092108-82-l) was converted to 3-(3,5- Difluorophenyl)pyrrolidine-l -carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.21 (2 H, br s), 7.09 (3H, m), 4.12 (0.5 H, br m), 3.89 (0.5 H, br m), 3.79 (0.5 H, br m), 3.45 (3 H, br m), 3.27 (0.5 H, m), 2.34 (0.5 H, br m), 2.20 (0.5 H, br m), 2.14 (0.5 H, br m), 1.99 (0.5 H, tar m).

¹³ C NMR (DMSC M): 178.5, 163.3, 163.2, 161.7, 161.6, 145.9, 110.6, 110.6, 110.5, 110.4, 102.4, 102.2, 102, 57, 53.4, 51.2, 47.3, 43.6, 42.1, 32.6, 31.4.

Example 13: 3-o-tolylpyrrolidine- -carbothioamide

3-(o-Tolyl)pyrrolidine (CAS#954220-67-8) was converted to 3-o-tolylpyrrolidine-l- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder

Ή NMR (DMSO- 6): 6.87 - 7.43 (6 H, m), 4.02 (0.5 H, m), 3.85 (0.5 H, m), 3.75 (0.5 H, m), 3.67 (0.5H, m), 3.51 - 3.62 (1.5 H, m), 3.47 (0.5 H, m), 3.40 (0.5 H, m), 3.23 (0.5 H, m), 2.32 (3 H, s), 2.30 (0.5H, m), 2.14 (0.5 H, m), 2.07 (0.5 H, m), 1.98 (0.5 H, m).

¹³ C NMR (DMSC M): 178.4, 139.5, 139.2, 135.9, 130.3, 126.5, 126.4, 126.2, 125.2, 125.1, 56.8, 53.2, 51, 47.1, 40.1, 38.5, 32.3, 30.9, 19.3.

Example 14: 3-m-tolylpyrrolidine- -carbothioamide

3-(m-Tolyl)pyrrolidine (CAS#954220-64-5) was converted to 3-m-tolylpyrrolidine-l- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as an off-white solid. Ή NMR (DMSO-ίΜ): 6.56-7.60 (2H, br s), 7.21 (1 H, t, J = 7.5 Hz), 7.11 (1 H, br s), 7.07 (1 H, br d, J = 6.3 Hz), 7.05 (1 H, br d, J = 7.5 Hz), 4.11 (0.5 H, m), 3.90 (0.5 H, m), 3.77 (0.5 H, m), 3.52 (1 H, m), 3.44 (1 H, m), 3.35 (1 H, m), 3.24 (0.5 H, m), 2.32 (0.5 H, m), 2.28 (3H, s), 2.18 (0.5 H, m), 2.08 (0.5 H, m), 1.96 (0.5 H, m).

1 ³ C NMR (DMSO- 6): 178.4, 178.4, 141.1, 141, 137.6, 128.4, 127.8, 127.4, 127.3, 124.1, 57.5, 53.9, 51.4, 47.5, 44, 42.3, 33,0, 31.8, 21.1.

Example 15: 3-(thiophen-3-yl)p

3-(Thiophen-3-yl)pyrrolidine (CAS#1231907-58-6) was converted to 3-(thiophen-3- yl)pyrrolidine-l -carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.51 (1 H, m), 7.28 (1 H, m), 7.18 (2 H, br s), 7.09 (1 H, m), 4.08 (0.5 H, br s), 3.85 (0.5 H, br s), 3.74 (0.5 H, m), 3.39-3.65 (2.5 H, m), 3.32 (0.5 H, m), 3.25 (0.5 H, m), 2.34 (0.5 H, br s), 2.18 (0.5 H, br s), 2.09 (0.5 H, m), 1.95 (0.5 H, m).

¹³ C NMR (DMSO- 6): 178.5, 178.4, 142.2, 127.2, 127.1, 126.5, 126.4, 120.7, 120.5, 57.2, 53.7, 51.2, 47.3, 39.8, 38.2, 32.9, 31.8.

Example 16: 3-(furan-3-yl)pyrro

3-(Furan-3-yl)pyrrolidine (CAS# 1260650-66-5) was converted to 3-(furan-3-yl)pyrrolidine-l- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a dark beige solid.

Ή NMR (DMSO-iM): 7.61 (1 H, s), 7.54 (1 H, s), 7.12 (2 H, m), 6.49 (1 H, dd, J = 1.8, 0.7 Hz), 4.01 (0.5 H, m), 3.81 (0.5 H, m), 3.67 (0.5 H, m), 3.31-3.57 (2.5 H, m), 3.24 (0.5 H, br s), 3.19 (0.5 H, m), 2.27 (0.5 H, br s), 2.12 (0.5 H, br s), 1.99 (0.5 H, m), 1.87 (0.5 H, m) . ¹³ C NMR (DMSO- 6): 178.5, 178.4, 143.5, 143.5, 138.9, 125.2, 110, 109.9, 57, 53.4, 51.1, 47.3, 35.1, 33.6, 32.5, 31.5.

Example 17: 3-(furan-2-yl)pyrro

3-(Furan-2-yl)pyrrolidine (CAS#1082926-03- 1) was converted to 3-(furan-2-yl)pyrrolidine-l- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white solid.

Ή NMR (DMSO- 6): 7.57 (1 H, s), 7.28 (2 H, br s), 6.38 (1 H, m), 6.21 (1 H, d, J = 3.1 Hz), 3.97 (0.5 H, br s), 3.77 (0.5 H, br s), 3.69 (0.5 H, br s), 3.52-3.66 (1.5 H, m), 3.30-3.51 (2 H, m), 2.31 (0.5 H, br s), 2.16 (0.5 H, m), 2.13 (0.5 H, m), 1.99 (0.5 H, br s).

¹³ C NMR (DMSC M): 178.6, 155.0, 154.8, 142.0, 110.4, 105.2, 105.0, 55.4, 51.8, 50.8, 47,0, 37.7, 36.1, 30.8, 29.6.

Example 18: 3-(2,5-difluorophenyl)pyrrolidine- 1 -carbothioamide

3-(2,5-Difluorophenyl)pyrrolidine (CAS#1203797-48-1) was converted to 3-(2,5- difluorophenyl)pyrrolidine-l -carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white solid.

Ή NMR (DMSO-iM): 6.82-7.61 (5 H, m), 4.09 (0.5 H, m), 3.90 (0.5 H, m), 3.76 (0.5 H, m), 3.71 (0.5 H, m), 3.46-3.64 (1 H, m), 3.38 (1 H, m), 2.33 (0.5 H, m), 2.18 (1 H, m), 2.03 (0.5 H, m). ¹³ C NMR (DMSO- 6): 178.5, 159.1, 157.6, 157.4, 155.7, 129.9, 117.0, 116.8, 114.9, 56.0, 52.4, 51.0, 47.0, 37.4, 35.9, 31.4, 30.3.

Example 19: 3-(2,4,5-trifluorophenyl)pyrrolidine- 1-carbothioamide

3-(2,4,5-Trifluorophenyl)pyrrolidine (CAS#1260814-64-9) was converted to 3-(2,4,5- trifluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white solid.

Ή NMR (DMSO- 6): 7.55 (2 H, m), 7.24 (2 H, br s), 4.09 (0.5 H, m), 3.90 (0.5 H, m), 3.76 (0.5 H, m), 3.69 (0.5 H, m), 3.52 (2 H, m), 3.37 (0.5 H, m), 3.29 (0.5 H, m), 2.31 (0.5 H, m), 2.17 (1 H, m), 2.03 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.5, 156.4, 154.8, 148.8, 147, 145.4, 125.1, 124.9, 116.5, 116.4, 116.3, 106.2, 106.0, 106.0, 105.8, 56.0, 52.5, 51.0, 47.0, 36.9, 35.4, 31.5, 30.4.

Example 20: 3-(3,4-difluorophen l)pyrrolidine- 1-carbothioamide

3-(3,4-Difluorophenyl)pyrrolidine (CAS#848822-98-0) was converted to 3-(3,4- difluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a light orange solid. Ή NMR (DMSO-ίΜ): 7.41 (2H, br m), 7.16 (1H, br s), 6.59-7.86 (2 H, m), 4.12 (0.5 H, m), 3.90 (0.5 H, m), 3.78 (0.5 H, m), 3.51 (1.5 H, m), 3.42 (1.5 H, m 1 H, s), 3.24 (0.5 H, m), 2.32 (0.5 H, m), 2.18 (0.5 H, m), 2.11 (0.5 H, m), 1.98 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.4, 150.2, 150.2, 149.1, 149.0, 148.6, 148.5, 147.5, 147.4, 139.0, 138.9, 124.0, 117.4, 117.3, 116.3, 116.2, 57.3, 53.8, 51.3, 47.4, 43.3, 41.7, 32.8, 31.7.

Example 21: (S)-3-(2,4,6-trifluorophenyl)pyrrolidine- 1-carbothioamide

(S)-3-(2,4,6-Trifluorophenyl)pyrrolidine (CAS#1335508-l l-6) was converted to (5)-3-(2,4,6- trifluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white solid.

Ή NMR (DMSO-iM): 7.22 (2 H, m), 6.50-8.0 (2H, m br), 4.03 (0.5 H, br m), 3.96 (0.5 H, br s),3.81 (0.5 H, br m), 3.68 (1 H, br m), 3.51-3.58 (1.5 H, m), 3.42 (0.5 H, br s), 3.38 (0.5 H, br s), 2.28 (1 H, m), 2.13 (1 H, br s).

1 ³ C NMR (DMSO-iM): 178.6, 162.1, 162, 160.5, 160.4, 112.2, 101.4, 101.2, 101.0, 54.6, 51.2, 50.8, 47.5, 33.7, 32.4, 30.8, 29.7.

Example 22: 3-(2,3,4-trifluorophen l)pyrrolidine- 1-carbothioamide

3-(2,3,4-Trifluorophenyl)pyrrolidine (CAS#1260884-52-3) was converted to 3-(2,3,4- trifluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as an off-white solid. Ή NMR (DMSO-ίΜ): 6.15-8.25 (2H, s br), 7.33 (1 H, br s), 7.21 (1 H, br s), 4.09 (0.5 H, br s), 3.88 (0.5 H, br s), 3.76 (1 H, m), 3.56 (1.5 H, m), 3.50 (0.5 H, br s), 3.30-3.50 (1 H, m), 2.37 (0.5 H, m), 2.18 (1 H, m), 2.03 (0.5 H, br s).

¹³ C NMR (DMSO-iM): 178.6, 178.5, 149.9, 149.7, 148.3, 148.1, 139.8, 138.2, 126.1, 122.4, 112.7, 55.9, 52.4, 50.9, 47.0, 37.0, 35.5, 31.6, 30.4.

Example 23: 3-(2,3,5,6-Tetrafluoro henyl)pyrrolidine- 1-carbothioamide

3-(2,3,5,6-Tetrafluorophenyl)pyrrolidine (CAS#1260865-90-4) was converted to 3-(2,3,5,6- Tetrafluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as an off-white powder.

Ή NMR (DMSO-iM): 7.84 (1 H, br s), 7.26 (2 H, br s), 4.10 (0.5 H, m), 3.95 (1 H, m), 3.78 (1 H, m), 3.47 (2 H, m), 3.41 (0.5 H, m), 2.0-2.40 (2H, m).

¹³ C NMR (DMSO-iM): 178.6, 146.5, 146.4, 146.3, 145.5, 144.8, 144.8, 144.7, 143.9, 143.8, 119.4, 105.6, 105.4, 54.3, 51.1, 50.6, 47.4, 34.7, 33.3, 30.7, 29.6.

Example 24: 3-(2,3,5-trifluorophenyl)pyrrolidine- 1-carbothioamide

3-(2,3,5-Trifluorophenyl)pyrrolidine (CAS#1260885-09-3) was converted to 3-(2,3,5- trifluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder. Ή NMR (DMSO-ίΜ): 7.45 (1 H, br s), 7.25 (2 H, br s), 7.13 (1H, m), 4.10 (0.5 H, m), 3.90 (0.5 H, m), 3.78 (1 H, m), 3.63 (0.5H, m), 3.53 (1.5 H, m), 3.41 (0.5 H, m), 3.35 (0.5 H, m), 2.35 (0.5H, m), 2.19 (1H, m), 2.04 (0.5H, m) .

¹³ C NMR (DMSC M): 178.5, 158.2, 158.1, 156.6, 156.5, 150.5, 150.4, 150.3, 148.9, 148.8, 148.7, 145.8, 144.2, 131.5, 110.1, 104.3, 55.8, 52.3, 50.9, 47, 37.3, 35.8, 31.5, 30.3.

Example 25: (S)-3-(3,5-difluorophenyl)pyrrolidine- 1-carbothioamide

(5)-3-(3,5-difluorophenyl)pyrrolidine (CAS#1336142-75-6) was converted to (5)-3-(3,5- difluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO- 6): 7.21 (2 H, br s), 7.07 (3 H, m), 4.12 (0.5 H, m), 3.89 (0.5 H, m), 3.78 (0.5

H, m), 3.35-3.63 (3 H, m), 3.27 (0.5 H, m), 2.34 (0.5 H, m), 2.20 (0.5 H, m), 2.14 (0.5 H, m),

I .99 (0.5 H, m).

1 ³ C NMR (DMSO-iM): 178.5, 163.3, 163.2, 161.7, 161.6, 146, 145.8, 110.6, 110.6, 110.5, 110.4, 102.3, 102.2, 102.0, 57, 53.4, 51.2, 47.3, 43.7, 42.1, 32.6, 31.4.

Example 26: ( ?)-3-(3,5-difluorophenyl)pyrrolidine- 1-carbothioamide

(tf)-3-(3,5-difluorophenyl)pyrrolidine (CAS#1334824-24-6) was converted to (R)-3-(3,5- difluorophenyl)pyrrolidine- 1-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder. Ή NMR (DMSO- 6): 7.21 (2 H, br s), 7.07 (3 H, m), 4.12 (0.5 H, m), 3.89 (0.5 H, m), 3.78 (0.5

H, m), 3.35-3.63 (3 H, m), 3.27 (0.5 H, m), 2.34 (0.5 H, m), 2.20 (0.5 H, m), 2.14 (0.5 H, m),

I.99 (0.5 H, m).

¹³ C NMR (DMSO-iM): 178.5, 163.3, 163.2, 161.7, 161.6, 146, 145.8, 110.6, 110.5, 110.4, 102.4, 102.2, 102.0, 57.0, 53.4, 51.2, 47.3, 43.7, 42.1, 32.6, 31.4.

Example 27: ( 15,55)- l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane-3-carbothioamide

(15,55)-l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane (CAS#1046141-90-5) was converted to (15,55)-l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane-3-carbot hioamide by a similar procedure as described for Example 10 and the product was isolated as a beige semi- solid.

Ή NMR (CDCls): 7.14 (1 H, br d, J = 4.4 Hz), 6.93 (1 H, dd, J = 5.1, 3.5 Hz), 6.89 (1 H, br), 5.81 (2 H, br s), 4.56 (0.5 H, m), 4.29 (0.5 H, m), 4.02 (0.5 H, m), 3.94 (0.5 H, m), 3.85 (0.5 H, m), 3.73 (1 H, m), 3.60 (0.5 H, br s), 1.97 (0.5 H, br s), 1.92 (0.5 H, br s), 1.39 (1 H, m), 0.96 (1 H, m).

¹³ C NMR (CDCI3): 180.2, 144.1, 143.8, 127, 124.2, 123.8, 123.6, 123.5, 58.9, 55.0, 54.8, 50.5, 28.6, 27.5, 27.2, 26.3, 20.1.

Example 28: (1 ?,5 ?)-l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane-3-carbothioam ide

(1 ?,5 ?)-l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane (CAS#1046141 -89-2) was converted to (1 ?,5 ?)-l-(thiophen-2-yl)-3-azabicyclo[3.1.0]hexane-3-carbothioam ide by a similar procedure as described for Example 10 and the product was isolated as a beige solid.

Ή NMR (DMSO-iM): 7.14 (1 H, br d, J = 4.4 Hz), 6.93 (1 H, dd, J = 5.1, 3.5 Hz), 6.89 (1 H, br), 5.75 (2 H, br s), 4.57 (0.5 H, m), 4.30 (0.5 H, m), 4.03 (0.5 H, m), 3.95 (0.5 H, m), 3.85 (0.5 H, m), 3.73 (1 H, m), 3.59 (0.5 H, br s), 1.98 (0.5 H, br s), 1.93 (0.5 H, br s), 1.39 (1 H, m), 0.96 (1 H, m).

¹³ C NMR (DMSC M): 180.3, 144.1, 143.8, 127, 124.2, 123.8, 123.6, 123.5, 58.9, 55.0, 54.8, 50.5 28.6, 27.5, 27.3, 26.3, 20.1.

3-(Perfluorophenyl)pyrrolidine (CAS#126Q650-30-3) was converted to 3- (perfluorophenyl)pyrrolidine- l-carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO- 6): 7.27 (2 H, br s), 4.09 (0.5 H, br s), 3.94 (1 H, br s), 3.77 (1 H, br s), 3.58 (1.5 H, br s), 3.46 (0.5 H, br s), 3.40 (0.5 H, br s), 2.37 (0.5 H, br s), 2.29 (0.5 H, br s), 2.23 (0.5 H, br s), 2.13 (0.5 H, br s).

¹³ C NMR (DMSC M): 178.6, 145.9, 144.3, 54.3, 51.1, 50.6, 47.3, 34.2, 32.8, 30.7, 29.7.

Example 30: ( IS,5R)- l-(3,5-Difluorophenyl)-N-methyl-3-azabicyclo[3.1.0]hexane-3- carbothioamide

A solution of (lS,5 ?)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) (0.215 g, 1.1 mmol) and methyl isothiocyanate (0.088 g, 1.210 mmol) in acetonitrile (5 mL) was stirred at room temperature for 4 h and then concentrated under reduced pressure. The residue was chromatographed (ethyl acetate - petroleum ether) to give ( IS,5R)- l-(3,5-difluorophenyl)-N-methyl-3-azabicyclo[3.1.0]hexane-3- carbothioamide as a yellowish solid (0.148 g, 50% yield). Ή NMR (CDCls): 6.60-6.71 (3 H, m), 5.51 (1 H, br s), 4.29 (1 H, br s), 3.96 (1 H, m), 3.81 (1 H, br d, J = 8.9 Hz), 3.75 (1 H, d, J = 7.5 Hz), 3.13 (3 H, d, J = 4.5 Hz), 2.02 (1 H, dt, J = 8.4, 4.4 Hz), 1.21 (1 H, dd, J = 5.4, 8.3), 0.94 (1 H, t, J = 4.9 Hz) .

¹³ C NMR (CDCI3): 181, 163.9, 163.8, 162.3, 162.2, 144.4, 144.4, 109.6, 109.5, 109.4, 109.4, 102.2, 102.1, 101.9, 55.5, 51.6, 32.4, 31.1, 24.7, 20.4.

Example 31; N-methyl-3-phenylpyrrolidine- 1 -carbothioamide

3-Phenylpyrrolidine (CAS#936-44-7) was converted to N-methyl-3-phenylpyrrolidine- l- carbothioamide by a similar procedure as described for Example 30 and the product was isolated as a white solid.

Ή NMR (CDCI3): 7.34 (2 H, t, J = 7.8 Hz), 7.27 (1 H, m), 7.23 (2 H, d, J = 7.9 Hz), 5.32 (1 H, br s), 3.68 - 4.46 (2 H, m), 3.62 (1 H, br s), 3.49 (1 H, br s), 3.17 (3 H, d, J = 4.55 Hz), 2.40 (1 H, br s), 2.07 - 2.20 (1 H, m).

¹³ C NMR (CDCI3): 179.8, 140.4, 128.7, 127.1, 126.9, 55.6, 49.2, 43.7, 32.7, 32.4.

Example 32; 3-(3,5-difluorophenyl)-N-methylpyrrolidine-l-carbothioamide

3-(3,5-Difluorophenyl)pyrrolidine (CAS#1092108-82- 1) was converted to 3-(3,5- difluorophenyl)-N-methylpyrrolidine- l-carbothioamide by a similar procedure as described for Example 30 and the product was isolated as a white solid.

Ή NMR (DMSO-iM): 7.31 (1 H, br q, J = 4.0 Hz), 7.11 (1 H, tt, J = 2.3, 9.3 Hz), 7.07 (2 H, m), 3.98 (1 H, br s), 3.73 (1 H, br m), 3.48 (2 H, br m), 3.39 (1 H, m), 2.89 (3 H, d, J = 4.3 Hz), 2.28 (1 H, br m), 2.07 (1 H, br m). ¹³ C NMR (DMSO-J6): 179.4, 163.8, 163.7, 162.2, 162.1, 146.5, 146.5, 146.4, 111, 110.9, 102.8, 102.6, 102.5, 56.2, 50.3, 43.1, 32.4, 32.1.

Example 33: N-methyl-3-(2,3,5,6-tetrafluorophenyl)pyrrolidine-l-carbothi oamide

3-(2,3,5,6-Tetrafluorophenyl)pyrrolidine (CAS# 1260865-90-4) was converted to N-methyl-3- (2,3,5,6-tetrafluorophenyl)pyrrolidine-l-carbothioamide by a similar procedure as described for Example 30 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.83 (1 H, m), 7.36 (1 H, br q, J = 3.7 Hz), 3.99 (1 H, br s), 3.83 (1 H, m), 3.77 (1 H, br s), 3.60 (1 H, m), 3.48 (1 H, m), 2.89 (3 H, d, J = 4.1 Hz), 2.31 (1 H, br s), 2.25 (1 H, br m).

¹³ C NMR (DMSO-iM): 179.1, 146.5, 146.4, 146.3, 145.5, 145.4, 144.9, 144.8, 144.7, 143.9, 143.8, 119.5, 119.4, 119.3, 105.7, 105.5, 105.3, 52.8, 48.4, 33.6, 32.0, 30.0. Example 34: l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio amide

l-(3,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio arriide by a similar procedure as described for Example 10 and the product was isolated as a white powder. Ή NMR (DMSO-iM): 7.30 (2 H, br s), 7.07 (1 H, br t, J = 9.2 Hz), 6.94 (2 H, br s), 4.39 (0.5 H, br s), 4.07 (0.5 H, br s), 3.92 (0.5 H, br s), 3.58-3.80 (2 H, m), 3.53 (0.5 H, br s), 2.21 (0.5 H, br s), 2.12 (0.5 H, br s), 1.20 (1 H, br s), 0.78 (1 H, br s).

¹³ C NMR (DMSC M): 179.9, 163.4, 163.3, 161.7, 161.6, 145.9, 145.9, 145.8, 109.8, 109.7, 109.5, 109.4, 101.8, 101.6, 101.5, 56.5, 53.7, 52.8, 49.9, 31.7, 30.1, 25.4, 24.7, 20.4, 20.0. Example 35: (1 ?,55)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1 ]hexane-3-carbothioamide

(1 ?,5S)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to (lR,55)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.30 (2 H, br s), 7.07 (1 H, br t, J = 9.2 Hz), 6.94 (2 H, br s), 4.39 (0.5 H, br s), 4.07 (0.5 H, br s), 3.92 (0.5 H, br s), 3.58-3.80 (2 H, m), 3.53 (0.5 H, br s), 2.21 (0.5 H, br s), 2.12 (0.5 H, br s), 1.20 (1 H, br s), 0.78 (1 H, br s).

¹³ C NMR (DMSC M): 179.9, 163.4, 163.3, 161.7, 161.6, 145.9, 145.9, 145.8, 109.7, 109.5, 101.8, 101.6, 101.4, 56.5, 53.7, 52.7, 50.0, 31.7, 30.2, 25.4, 24.7, 20.4, 20.0.

Example 36: ( IS,5R)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio amide

(15,5 ?)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to (15,5R)- l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carbothioamide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.30 (2 H, br s), 7.07 (1 H, br t, J = 9.2 Hz), 6.94 (2 H, br s), 4.39 (0.5 H, br s), 4.07 (0.5 H, br s), 3.92 (0.5 H, br s), 3.58-3.80 (2 H, m), 3.53 (0.5 H, br s), 2.21 (0.5 H, br s), 2.12 (0.5 H, br s), 1.20 (1 H, br s), 0.78 (1 H, br s). ¹³ C NMR (DMSC M): 179.9, 163.4, 163.3, 161.7, 161.6, 145.9, 145.9, 109.7, 109.5, 101.8, 101.6, 101.4, 56.5, 53.7, 52.8, 50, 31.7, 30.2, 25.5, 24.7, 20.4, 20.0,

Example 37: l-(2,4-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio amide

l-(2,4-Difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to l-(2,4-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio amide by a similar procedure as described for Example 10 and the product was isolated as a white powder. Ή NMR (DMSO-iM): 7.42 (1 H, m), 7.24 (1 H, br t, J = 9.3 Hz), 7.05 (1 H, br t, J = 7.5 Hz), 6.80-7.60 (2H, br s), 4.30 (0.5 H, m), 4.09 (0.5 H, m), 3.87 (0.5 H, m), 3.71 (0.5 H, m), 3.66 (0.5 H, m), 3.58 (0.5 H, m), 3.48 (0.5 H, m), 3.35 (0.5 H, m), 2.09 (0.5 H, m), 1.93 (0.5 H, m), 1.10 (1 H, br s), 0.70 (1 H, t, J = 4.7 Hz).

¹³ C NMR (DMSC M): 179.8, 162.7, 162.6, 162.3, 162.2, 161, 160.9, 160.7, 160.6, 131.9, 123.5, 111.5, 111.3, 104.2, 104.0, 103.9, 57.9, 54.1, 53.9, 50.0, 27.6, 26.2, 22.8, 21.8, 16.8, 16.7.

Example 38: 1 - (2, 5 -difluoro - carbothio amide

l-(2,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to l-(2,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio amide by a similar procedure as described for Example 10 and the product was isolated as a white powder.

Ή NMR (DMSO-iM): 7.20-7.28 (2 H, m), 7.16 (1 H, m), 6.60-8.00 (2H, br s), 4.33 (0.5 H, br m), 4.09 (0.5 H, br m), 3.90 (0.5 H, br m), 3.71 (0.5 H, br m), 3.65 (0.5 H, br m), 3.46-3.61 (1H, m), 3.40 (0.5 H, br m), 2.18 (0.5 H, br m), 2.03 (0.5 H, br m), 1.14 (1 H, br s), 0.73 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-iM): 179.8, 158.8, 157.2, 129.2, 117, 117, 116.9, 116.8, 115.4, 115.3, 57.5, 53.8, 49.9, 28.2, 26.7, 23, 22.1, 17.4, 17.1. Example 39: ( IS,5R)- l-(3,5-Difluorophenyl)-N-propyl-3-azabicyclo[3.1.0]hexane-3- carbothioamide

Step 1: ((lS,5R)-l-( 3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl)( lH-imidazol-1 - yl)methanethio

To a solution of Ι, -thiocarbonyldiimidazole (0.329 g, 1.844 mmol) in dry tetrahydrofuran (6 mL) was added a solution of (lS,5 ?)-l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) (0.36 g, 1.844 mmol) in dry tetrahydrofuran (6 mL). The solution was stirred at room temperature for 1 h and then at 50-55 °C for 2 h. After being cooled to room temperature, the solution was concentrated under reduced pressure. The residue was chromatographed (ethyl acetate - petroleum ether) to give (( 15,57?)- 1 -(3,5- difluorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl)(lH-irnidazol- l-yl)methanethione (0.31 g, 55% yield).

Step 2: (lS,5R)-l-( -Difluorophenyl)-N-propyl-3-az bicyclo[3.1.0]hexane-3-carbothioamide

To a solution of ((15,5 ?)-l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl)(lH- imidazol-l- yl)methanethione (0.15 g, 0.491 mmol) in dry tetrahydrofuran (3 mL) was added propan-1 -amine (0.081 mL, 0.982 mmol) and the mixture was stirred at 65 °C for 16 h. The solvents were evaporated off and then the residue was chromatographed (petroleum ether - ethyl acetate) to give (15,5 ?)-l-(3,5-difluorophenyl)-N-propyl-3-azabicyclo[3.1.0]hexane -3-carbothioamide as a yellowish viscous oil (0.093 g, 64% yield).

Ή NMR (CDCls): 6.65-6.74 (3 Η, m), 5.30 (1 Η, t, J = 4.7 Hz), 4.29 (1 H, br m), 3.96 (1 H, br m), 3.82 (1 H, br d, J = 8.9 Hz), 3.76 (1 H, br d, J = 7.0 Hz), 3.60 (2 H, m), 2.03 (1 H, dt, J = 4.3, 8.3 Hz), 1.65 (2 H, m), 1.23 (1 H, d m, J = 5.3 Hz), 0.97 (3 H, t, J = 7.5 Hz), 0.97 (1H, m) . ¹³ C NMR (CDCls): 180.2, 164, 163.9, 162.3, 162.2, 144.5, 144.4, 144.4, 109.7, 109.6, 109.5, 109.5, 102.3, 102.1, 102.0, 55.4, 51.5, 47.4, 31.1, 24.7, 22.5, 20.3, 11.4.

Example 40: l-(2,5-difluorophenyl)-N-(2-mercaptoethyl)-3-azabicyclo[3.1. 0]hexane-3- carbothioamide

l-(2,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to l-(2,5-difluorophenyl)-N-(2-mercaptoethyl)-3-azabicyclo[3.1. 0]hexane- 3-carbothioamide by a similar procedure as described for Example 39 and the product was isolated as a colourless oil.

Ή NMR (DMSO-iM): 7.56 (1 H, t br, J = 4.5 Hz), 7.24 (2 H, m), 7.16 (1 H, m), 4.17 (1H, s br), 3.91 (1H, s br), 3.67 (1 H, m), 3.56 (2 H, m), 3.50 (1 H, br s), 2.63 (2 H, q, J = 7.1 Hz), 2.39 (1 H, m), 2.14 (1 H, br s), 1.13 (1 H, dd, J = 8.0, 5.1 Hz), 0.76 (1 H, t, J = 4.8 Hz).

1 ³ C NMR (DMSC M): 179.3, 158.8, 158.7, 157.2, 157.1, 129.3, 129.3, 129.2, 129.2, 117.0, 117.0, 117.0, 116.9, 116.9, 116.8, 115.5, 115.4, 115.3, 115.2, 53.6, 49.6, 47.8, 47, 27.1, 22.8, 22.2, 17.6.

Example 41: ( IS,5R)- l-(3,5-difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3.1.0]hex ane-3- carbothioamide

To a solution of (1 ?,55)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexan-2-one (Example 60, step 2) (0.628 g, 3 mmol) in dry tetrahydrofuran (15 mL) was added sodium hydride (60% in mineral oil) (0.180 g, 4.5 mmol) at 0-5 °C in portions. The mixture was stirred for 30 min at room temperature, and methyl isothiocyanate (0.329 g, 4.5 mmol) was then added at -78 °C. The mixture was allowed to reach room temperature over 3 h, then carefully quenched with aq. ammonium chloride solution, and extracted with a mixture of ethyl acetate - petroleum ether (2: 1). The organic phase was dried over MgSC and evaporated to dryness. The residue was triturated with petroleum ether, then filtered, washed with petroleum ether, and dried under vacuum. Chromatography (ethyl acetate - petroleum ether; 1 : 4) afforded ( 15,57?)- 1 -(3,5- difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3.1.0]hexane-3-c arbothioamide as a white powder (0.036 g, 4% yield).

Ή NMR (DMSO-iM): 10.37 (1 H, br s), 7.18 (2 H, m), 7.15 (1 H, tt, J = 2.3, 9.3 Hz), 4.50 (1 H, dd, J = 11.4, 1.7 Hz), 4.16 (1 H, d, J = 11.3 Hz), 3.02 (3 H, d, J = 2.8 Hz), 2.76 (1 H, ddd, J = 1.7, 3.5, 9.1 Hz), 1.68 (1 H, dd, J = 9.1, 4.8 Hz), 1.43 (1 H, dd, J = 4.8, 3.6 Hz).

1 ³ C NMR (DMSO-iM): 180.5, 174.4, 163.3, 163.2, 161.7, 161.6, 143.3, 143.3, 143.2, 111.0, 111.0, 110.9, 110.8, 102.9, 102.7, 102.6, 56.1, 32.1, 30.1, 26.8, 26.7, 26.7, 20.7.

Example 42: 4-(3,5-difluorophen l)-N-methyl-2-oxopyrrolidine- 1 -carbothioamide

4-(3,5-Difluorophenyl)pyrrolidin-2-one (CAS#1604786-89- l) was converted to 4-(3,5- difluorophenyl)-N-methyl-2-oxopyrrolidine- l-carbothioamide by a similar procedure as described for Example 41 and the product was isolated as a beige powder.

Ή NMR (DMSO-iM): 10.51 (1 H, br q, J = 4.5 Hz), 7.10-7.20 (3 H, m), 4.54 (1 H, dd, J = 10.7, 8.2 Hz), 3.85 (1 H, dd, J = 10.8, 9.0 Hz), 3.68 (1 H, quin, J = 9.0 Hz), 3.05 (3 H, d, J = 4.5 Hz), 2.95-3.05 (2H, m).

1 ³ C NMR (DMSO-iM): 180.1, 174.7, 163.3, 163.3, 161.7, 161.6, 145.5, 145.4, 145.3, 110.8, 110.7, 110.6, 110.6, 102.7, 102.5, 102.4, 56.7, 40.3, 35.1, 32.2.

Example 43: l-(3,5-Difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3.1.0]hex ane-3- carbothioamide

5-(3,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexan-2-one was converted to l-(3,5- Difluorophenyl)-N-methyl-4-oxo-3-azabicyclo[3.1 ]hexane-3-carbothioamide by a similar procedure as described for Example 41 and the product was isolated as a beige powder.

Ή NMR (DMSO- 6): 10.37 (1 H, q, J = 4.5 Hz), 7.18 (2 H, m), 7.15 (1 H, tt, J = 2.3, 9.3 Hz), 4.50 (1 H, dd, J = 11.4, 1.7 Hz), 4.16 (1 H, d, J = 11.3 Hz), 3.02 (3 H, d, J = 4.5 Hz), 2.76 (1 H, ddd, J = 1.7, 3.5, 9.1 Hz), 1.68 (1 H, dd, J = 9.1, 4.8 Hz), 1.43 (1 H, dd, J = 4.8, 3.6 Hz) .

1 ³ C NMR (DMSO-iM): 180.5, 174.4, 163.3, 163.2, 161.7, 161.6, 143.3, 143.3, 143.2, 111.0, 111.0, 110.9, 110.8, 102.9, 102.7, 102.5, 56.1 , 32.1, 30.1, 26.7, 26.7, 20.7.

Example 44: 6-Phenyltetrahydro- lH-pyrrolo[l,2-c]imidazole-3(2H)-thione

A solution of Ι, Γ-thiocarbonyldiimidazole (0.159 g, 0.894 mmol) in dichloromethane (2 mL) was added dropwise to a solution of (4-phenylpyrrolidin-2-yl)methanamine (CAS# 82256-70-0) (0.150 g, 0.851 mmol) in dichloromethane (2 mL) at room temperature. The thus obtained orange solution was allowed to stir at room temperature for 1 h, diluted with dichloromethane, and then washed with water. The organic layer was dried over MgSC and evaporated under vacuum to give the crude product as an orange oil. Chromatography (dichloromethane - methanol) followed by trituration (petroleum ether - ethyl acetate) afforded 6-phenyltetrahydro- lH-pyrrolo[l,2-c]imidazole-3(2H)-thione as a beige solid (0.076 g, 41% yield).

Ή NMR (DMSO-iM): 8.61 (1 Η, s), 7.31 (2 Η, t, J = 7.5 Hz), 7.25 (2 H, d, J = 8.6 Hz), 7.22 (1 H, t m, J = 7.2 Hz), 4.17 (1 H, m, J = 10.1, 4.5 Hz), 3.74 (1 H, dd, J = 7.3, 10.3 Hz), 3.67 (1 H, t, J = 9.8 Hz), 3.60 (1H, t, J = 9.3 Hz), 3.55 (1H, m), 3.44 (1 H, dd, J = 3.7, 10.4 Hz), 2.26 (1 H, m), 1.50 (1 H, q, J = 11.3 Hz).

¹³ C NMR (DMSO-iM): 186.3, 142.6, 128.6, 127.1, 126.5, 63.1, 54.2, 46.2, 45, 39.2. Example 45: l-(3,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothio hydrazide

Step -(3-phenylpyrrolidine-l-carbonothioyl)benz mide

To a solution of Ι,Γ-thiocarbonyldiimidazole (201 mg, 1.127 mmol) in anhydrous tetrahydrofuran (2.6 mL) was added dropwise a solution of l-(3,5-difluorophenyl)-3- azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) (200 mg, 1.025 mmol) in anhydrous tetrahydrofuran (2.6 mL) at room temperature. The reaction was stirred at room temperature for 1 h, then heated at 55 °C for 2 h. Thereupon, the solvent was evaporated off and the resulting yellow oil was dissolved in methanol (2.5 mL) followed by addition of benzyl carbazate (341 mg, 2.049 mmol) in one portion. The reaction was heated at reflux temperature for 24 h, the solvent was then evaporated off and the residue was dissolved in dichloromethane, washed with water, dried over MgSC , filtered and evaporated to dryness. The thus obtained yellow oil was purified by chromatography (dichloromethane - methanol) to give benzyl 2-(l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carbonothioyl)hydrazinecarboxylate as a yellow oil (0.27 g, 0.67 mmol, 65% yield).

Step 2: N- -phenylpyrrolidine-l-carbonothioyl)benz mide

To a stirred solution of benzyl 2-(l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carbonothioyl)hydrazinecarboxylate (270 mg, 0.67 mmol) in dichloromethane (5 mL) was added dropwise boron tribromide (0.19 mL, 2.008 mmol) at -78 °C under nitrogen. The solution was stirred in the cold for 5 min, then was allowed to warm up to room temperature naturally and stirred for 1.5 h. The mixture was then cooled again to 0-5 °C followed by quenching with water. The resulting emulsion then was extracted with a mixture of 30% 2-propanol in dichloromethane, the organic phase was washed with water, dried over MgSC , filtered and evaporated to dryness. The thus obtained yellow oil was purified by chromatography (dichloromethane - methanol), Recrystallization from 2-propanol afforded l-(3,5- difluorophenyl)-3-azabicyclo[3.1.0]hexane-3-carbothiohydrazi de as a pink solid (0.015 g, 8% yield).

Ή NMR (DMSO-iM): 8.80 (1 H, s), 7.08 (1 H, tt, J = 9.4, 2.4 Hz), 6.95 (2 H, m), 4.64 (2 H, br s), 4.17 (1 H, br d, J = 10.9 Hz), 3.89 (1 H, br d, J = 11.0 Hz), 3.68 (1 H, d, J = 10.9 Hz), 3.59 (1 H, br dd, J = 10.9, 4.2 Hz), 2.18 (1 H, dt, J = 8.3, 4.2 Hz), 1.19 (1 H, dd, J = 8.0, 5.1 Hz), 0.77 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 180.7, 163.4, 163.3, 161.8, 161.7, 146, 145.9, 145.8, 109.7, 109.7, 109.6, 109.5, 101.8, 101.7, 101.5, 54.4, 51.7, 30.4, 24.6, 20.3.

Example 46: l-(3,5-Difluorophenyl)-N,N-dimethyl-3-azabicyclo[3.1.0]hexan e-3- carbothioamide

To a solution of Ι, Γ-thiocarbonyldiimidazole (201 mg, 1.127 mmol) in anhydrous tetrahydrofuran (2.6 mL) was added dropwise a solution of l -(3,5-difluorophenyl)-3- azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) (200 mg, 1.025 mmol) in anhydrous tetrahydrofuran (2.6 mL) at room temperature. The solution was stirred at room temperature for 1 h, then was heated at 55 °C for 2 h. The solvent was evaporated off under vacuum and the oily residue was dissolved in methanol (4.1 mL), followed by addition of 1, 1- dimethylhydrazine (0.13 mL 1.690 mmol). The mixture was then heated to reflux and stirred for 24 h, and then cooled to room temperature, whereupon the solvent was evaporated off. The yellow oily residue was dissolved in dichloromethane, washed with water, dried over MgS0 ₄ , filtered and evaporated to dryness. Chromatography (petroleum ether - ethyl acetate) afforded 1- (3,5-difluorophenyl)-N,N-dimethyl-3-azabicyclo[3.1.0]hexane- 3-carbothioamide as a light yellow oil (0.124 g, 26% yield).

Ή NMR (CDCls): 6.70 (2 H, m), 6.67 (1 H, tt, J = 2.3, 8.9 Hz), 4.59 (1 H, d, J = 11.0 Hz), 4.16 (1 H, d, J = 11.0 Hz), 3.72 (1 H, dd, J = 3.6, 10.9 Hz), 3.71 (1 H, dd, J = 1.2, 10.9 Hz), 3.13 (6 H, m), 1.84 (1 H, m), 1.07 (1 H, m), 0.98 (1 H, m) .

¹³ C NMR (CDCls): 191.7, 163.9, 163.8, 162.3, 162.2, 144.8, 109.7, 109.7, 109.6, 109.6, 102.1, 101.9, 101.7, 57.2, 54.4, 43.2, 30.0, 24.3, 17.4. N-(cyanomethyl)- l-(2,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-

l-(2,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane (Feng Xu et al.: Org. Lett. 8(17), 3885-3888, 2006) was converted to N-(cyanomethyl)- l-(2,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carbothioamide by a similar procedure as described for Example 30 and the product was isolated as a brownish red solid.

Ή NMR (DMSO-iM): 7.99 (1 H, br s), 7.25 (2 H, m), 7.17 (1 H, m), 4.45 (2 H, br d, J = 5.1 Hz), 3.44-4.40 (4H, br m), 2.19 (1 H, br s), 1.16 (1 H, m), 0.80 (1 H, m) .

¹³ C NMR (DMSC M): 179.7, 158.8, 158.7, 157.2, 157.1, 129.1, 129.1, 129.0, 129.0, 129.0, 129.0, 117.6, 117.1, 117.0, 117.0, 116.9, 116.8, 116.8, 115.5, 115.5, 115.4, 115.3, 58.3, 54.5, 53.6, 49.9, 33.2, 28.1, 26.4, 23, 21.6, 17.8. Example 48: 3-(3,5-Difluorophenyl)-N-methyl-2,3-dihydro- lH-pyrrole- 1 -carbothioamide Step 1: 4-( 3, 5-difluorophenyl)-2-hydroxy-N-methylpyrrolidine-l -carbothioamide

To a solution of 4-(3,5-difluorophenyl)-N-methyl-2-oxopyrrolidine- l-carbothioamide (Example 42) (0.270 g, 1 mmol) in dry toluene (5 mL) was added dropwise 1 M diisobutylaluminum hydride (2.70 mL, 2.70 mmol) in toluene at 0-5 °C and the reaction was stirred for 1 h in the cold. Thereupon, the mixture was quenched with ice-water, stirred for 1 h in the cold, diluted with ethyl acetate (20 mL) and then filtered through a celite plug. The organic phase was dried over MgS0 ₄ and evaporated to dryness. Purification by chromatography (petroleum ether - ethyl acetate) afforded 4-(3,5-difluorophenyl)-2-hydroxy-N-methylpyrrolidine- l-carbothioamide as a white powder (0.14 g, 51% yield).

Step 2: 3-(3,5-Difluorophenyl)-N-methyl-2, 3 -dihydro-lH-pyrrole-1 -carbothioamide

To a solution of 4-(3,5-difluorophenyl)-2-hydroxy-N-methylpyrrolidine-l-carbo thioamide (0.2 g, 0.734 mmol) in dry toluene (5 mL) was added 2,6-lutidine (0.428 mL, 3.67 mmol) followed by addition of 2,2,2-trifluoroacetic anhydride (0.23 mL, 1.76 mmol) at -10 °C under nitrogen. The reaction was allowed to warm up to room temperature and stirred for 20 h. Thereupon, the mixture was quenched with water (10 mL) and stirred for 30 min. The organic phase was evaporated to dryness, the residue was then dissolved in ethanol (15 mL) and treated with 5 M sodium hydroxide (0.3 mL, 1.469 mmol) at room temperature for 1 h. Thereupon, the mixture was evaporated to dryness and the residue was partitioned between dichloromethane and water. The organic phase was dried over MgSC , evaporated to dryness under vacuum and chromatographed (petroleum ether - ethyl acetate) to give 3-(3,5-difluorophenyl)-N-methyl-2,3- dihydro-lH-pyrrole-l-carbothioamide as a white powder (0.063 g, 33% yield).

Ή NMR (DMSO-iM): 7.80 (1 Η, br s), 7.41 (1 Η, br d, J = 2.3 Hz), 7.11 (1 H, m), 6.93 (2 H, m), 5.37 (1 H, dd, J = 4.1, 2.6 Hz), 4.37 (1 H, m), 4.23 (1 H, t, J = 11.2 Hz), 3.70 (1 H, dd, J = 11.6, 5.7 Hz), 2.91 (3 H, d, J = 4.3 Hz).

¹³ C NMR (DMSO-iM): 176.6, 163.5, 163.4, 161.8, 161.8, 148.5, 148.4, 148.3, 133.4, 112.2, 110.4, 110.2, 102.6, 102.4, 102.2, 55.9, 46.6, 31.9.

Example 49: 6-phenyl-6,7-dihydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione

Step 1: 2-phenylpe -4-enenitrile

To a stirred solution of 2-phenylacetonitrile (3.15 mL, 27.3 mmol) in tetrahydrofuran ( 136 mL) was added lithium hexamethyldisilazane (30 mL, 30.0 mmol) dropwise at -78 °C. The resulting yellow solution was allowed to stir in the cold for 30 min, whereupon 3-bromoprop-l-ene (2.3 mL, 27.2 mmol) was added dropwise and the mixture was stirred at room temperature. The solvent was then removed under vacuum and the product was purified by chromatography (petroleumether - ethyl acetate; 1:0, 9: 1, then 6: 1) and isolated as a yellow oil. (Yield: 2.62g, 63%).

Step 2: 2-phenylpent-4-en-l -amine

To a stirred solution of 2-phenylpent-4-enenitrile (2.82 g, 17.94 mmol) in dry tetrahydrofuran (60 mL) was added lithium aluminum hydride (1.362 g, 35.9 mmol) portionwise at 0 °C. The thus obtained pink suspension was allowed to stir at room temperature for 5 min and then at 60 °C overnight. Thereupon, water (1.5 mL) was added followed by slow addition of a mixture of 50% sodium hydroxide (1.5 mL) and water (3 mL) at 0 °C. The organic layer was diluted with a mixture of dichloro methane - 2-propanol (7:3), dried over MgS0 ₄ and filtered through a celite plug. The filtrate was evaporated to dryness under vacuum to give a clear oil. The product was purified by chromatography (dichloromethane - methanol) and isolated as a dark yellow oil. (Yield: 1.13 g, 39%).

Ste -methyl-N-(2-phenylpent-4-en-l-yl)benzenesulfonamide

To a stirred solution of 2-phenylpent-4-en- 1 -amine (1.13 g, 7.01 mmol) and triethylamine (1.074 mL, 7.71 mmol) in dichloromethane (35 mL) was added tosyl chloride (1.336 g, 7.01 mmol) portionwise at room temperature. The resulting yellow solution was allowed to stir at room temperature overnight. The reaction was then diluted with dichloromethane and quenched with water. The organic layer was separated, dried over MgS0 ₄ and evaporated to dryness under vacuum to give a yellow oil. The product was purified by chromatography (petroleum ether - ethyl acetate 1:0, 9: 1, 6: 1, then 4: 1) and isolated as a yellow oil. (Yield: 1.03 g, 44%).

Step 4: (4-phenyl-l-tosylpyrrolidin-2-yl)methanol

3- Chlorobenzoperoxoic acid (0.676 g, 3.92 mmol) was added portionwise to a stirred solution of

4- methyl-N-(2-phenylpent-4-enyl)benzenesulfonamide (1.03 g, 3.27 mmol) in dichloro methane (16 mL) at 0 °C. The reaction mixture was allowed to warm up to room temperature and stirred for 2 days. Thereupon, water was added, the organic layer was diluted with dichloro methane, separated, dried over MgSC and evaporated to dryness under reduced pressure. The product was purified by chromatography (petroleum ether - ethyl acetate; 1: 1) and isolated as a clear oil. (Yield: 0.215 g, 20%).

Step 5: (4- henylpyrrolidin-2-yl)methanol

Lithium aluminium hydride (0.223 g, 5.88 mmol) was added portionwise to a stirred solution of (4-phenyl-l-tosylpyrrolidin-2-yl)methanol (0.487 g, 1.469 mmol) in dry terahydrofuran (7 mL) at 0 °C under nitrogen. The thus obtained grey suspension was allowed to stir at room temperature overnight, whereupon the reaction was quenched with water (0.3 mL) followed by dropwise addition of a mixture of 50% NaOH (0.3 mL) and water (0.6 mL). The mixture was then dried over MgSC and filtered through a celite plug. The filtrate was evaporated to dryness under vacuum to give a semisolid on trituration with ethyl acetate. The solid was suspended in ethyl acetate, filtered off and the filtrate was evaporated to dryness to leave a clear oil. (Yield: 0.318 g, 122% (intermediate not purified prior to next step)).

Step 6: tert- tyl 2-(hydroxymethyl)-4-phenylpyrrolidine-l-carboxylate

To a stirred solution of (4-phenylpyrrolidin-2-yl)methanol (0.260 g, 1.467 mmol) in ethanol (3 mL) was added di-ie/t-butyl dicarbonate (0.352 g, 1.614 mmol) at 0 °C. The resulting yellow solution was allowed to stir at room temperature overnight. The solvent was then evaporated to dryness under vacuum and the thus obtained mixture was separated by chromatography (petroleum ether - ethyl acetate (1 :0, 3: 1, 2: 1, then 1 : 1). The product was isolated as a clear oil. (Yield: 0.298 g, 73%).

Step 7: tert-but l 2-formyl-4-phenylpyrrolidine-l-carboxylate

Dess-Martin periodinane (3-oxo- l ⁵ -benzo[<i] [l,2]iodaoxole- l, l, l(3H)-triyl triacetate) (0.443 g, 1.046 mmol) was added in one portion to a stirred solution of tert-butyX 2-(hydroxymethyl)-4- phenylpyrrolidine- l-carboxylate (0.290 g, 1.046 mmol) in dichloromethane (13 mL) at room temperature and the reaction was then stirred for 3 h. Thereupon, the solvent was evaporated off and the resulting residue was azeotroped with toluene. The product was purified by chromatography (petroleum ether - ethyl acetate; 1 :0, 4: 1, 3: 1, 2: 1, 1 : 1) and isolated as a clear oil. (Yield: 0.234 g, 81%).

Step 8: 4-phenylpyrrolidine-2-carbaldeh de hydrochloride

A 2 M solution of HCI (3.34 mL, 6.68 mmol) in diethyl ether was added to tert-butyX 2-formyl- 4-phenylpyrrolidine- l-carboxylate (0.230 g, 0.835 mmol) at room temperature and the thus obtained yellow mixture was allowed to stir at room temperature for 3 h. The solvent was then evaporated off under vacuum to leave a yellow oil. (Yield: 0.177 g, 100%).

Step 9: 6-phenyl-6,7-dihydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione

To a stirred solution of 4-phenylpyrrolidine-2-carbaldehyde hydrochloride (0.177 g, 0.836 mmol) in dimethyl formamide (3.5 mL) was added potassium thiocyanate (0.163 g, 1.672 mmol) and the thus obtained yellow solution was allowed to stir at 100 °C for 1 h and 45 min to give a brown solution. The reaction mixture was allowed to cool to room temperature, and then diluted with water (3 mL) and diethyl ether, respectively. The aqueous layer was extracted with ethyl acetate (3 times) and the combined organic layers were washed with water (twice), dried over MgS0 ₄ and evaporated to dryness under vacuum to give a brown solid. Recrystallization from isopropanol afforded a beige solid. (Yield: 24 mg, 12%).

Ή NMR (DMSO-iM): 11.78 (1 H, br s), 7.15-7.45 (5 H, m), 6.63 (1 H, s), 4.17 (1 H, dd, J = 11.2, 8.1 Hz), 4.08 (1 H, quin, J = 8.1 Hz), 3.67 (1 H, dd, J = 11.2, 8.1 Hz), 3.24 (1 H, ddd, J = 15.0, 7.9, 0.7 Hz), 2.86 (1 H, ddd, J = 15.4, 8.5, 1.5 Hz) .

¹³ C NMR (DMSO-iM): 155.9, 141.3, 132.7, 128.7, 127.2, 127.0, 106.7, 50.4, 47.0, 31.2. Example 50: 6-(3,5-difluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2-c]imidazol e-3(5H)-thione

2-(3,5-difluorophenyl)acetonitrile was converted to 6-(3,5-difluorophenyl)-6,7-dihydro-2H- pyrrolo[l,2-c]imidazole-3(5H)-thione by a similar procedure as described for Example 49 and the product was isolated as a dark beige solid.

Ή NMR (DMSO-iM): 11.81 (1 Η, br s), 7.11-7.18 (3 Η, m), 6.64 (1 Η, m), 4.19 (1 Η, dd, J =

11.2, 7.9 Hz), 4.12 (1 H, quin, J = 8.3 Hz), 3.70 (1 H, dd, J = 11.2, 8.5 Hz), 3.23 (1 H, ddd, J =

15.3, 7.9, 0.9 Hz), 2.90 (1 H, ddd, J = 15.3, 8.9, 1.6 Hz) . ¹³ C NMR (DMSO-iM): 163.3, 163.2, 161.7, 161.6, 156.0, 145.5, 145.4, 145.4, 132.3, 110.8, 110.8, 110.7, 110.7, 106.8, 102.7, 102.5, 102.3, 49.9, 46.6, 30.8.

Example 51; 6-(2,4-Difluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2-c]imidazol e-3(5H)-thione Step 1: (E)-N-(2-(2,4-difluorophenyl)-3-(dimethylamino)allylidene)-N -methylm

hexafluoropho sphate( V)

Phosphoryl trichloride (8.12 mL, 87 mmol) was added dropwise to N,N-dimethylformamide (8.32 mL, 107 mmol) at 0 °C to give a clear viscous solution. The mixture was allowed to warm up to room temperature and stirred for 1 h before adding a solution of 2-(2,4- difluorophenyl) acetic acid (5 g, 29.0 mmol) in N,N-dimethylformamide (15 mL). The resulting yellow solution was allowed to stir at 70 °C overnight. The thus obtained brown reaction mixture was cooled to room temperature and slowly poured onto a mixture of ice-water (60 mL) and a solution of potassium hexafluoropho sphate(V) (8.02 g, 43.6 mmol) in water (20 mL). The resulting yellow precipitate was filtered off, washed with cold water and dried under vacuum. (Yield: 10 g, 85%).

Step 2: ethyl 4-(2,4-difluorophenyl)-lH-pyrrole-2-carboxylate

To a stirred solution of ethyl 2-aminoacetate hydrochloride (5.45 g, 39.0 mmol) and (E)-N-(2- (2,4-difluorophenyl)-3-(dimethylamino)allylidene)-N-methylme thanaminium

hexafluoropho sphate(V) (10 g, 26.0 mmol) in N,N-dimethylformamide (240 mL) was added 1,4- diazabicyclo[2.2.2]octane (7.30 g, 65.1 mmol) at room temperature and the thus obtained yellow suspension was allowed to stir at 100 °C overnight. The mixture was then poured onto ice-water (ca. 400 mL) and allowed to stir at room temperature for 1 h. The resulting precipitate was filtered off, washed with water to give the product as a brown solid. (Yield: 4.5 g, 65%).

Step 3: 1-tert-butyl 2-ethyl 4-(2,4-difluorophenyl)-lH-pyrrole-l ,2-dicarboxylate

To a stirred solution of ethyl 4-(2,4-difluorophenyl)-lH-pyrrole-2-carboxylate (4.5 g, 17.91 mmol) and di-ie/t-butyl dicarbonate (4.30 g, 19.70 mmol) in acetonitrile (90 mL) was added N,N-dimethylpyridin-4-amine (0.219 g, 1.791 mmol) at room temperature. The resulting clear solution was allowed to stir at room temperature overnight. Thereupon, the reaction mixture was quenched with water, the organic layer was diluted with dichloro methane, separated, dried over MgS0 ₄ and evaporated to dryness under vacuum to give a brown oil. The product was purified by chromatography (petroleum ether - ethyl acetate; 1:0, 8: 1, then 6: 1) and isolated as a yellow oil. (Yield: 5.46 g, 82%).

Step 4: 1-tert-butyl 2-ethyl 4-(2,4-difluorophenyl)pyrrolidine-l,2-dicarboxylate

A solution of l-ie/t-butyl 2-ethyl 4-(2,4-difluorophenyl)-lH-pyrrole-l,2-dicarboxylate (4.5 g, 12.81 mmol) in ethanol (128 mL) was added to 10% palladium on charcoal (0.341 g, 0.320 mmol) at room temperature under nitrogen. The mixture was allowed to stir at 60 °C under 10 bar of hydrogen for 3h. Thereupon, the mixture was cooled to room temperature, purged with argon, filtered through a celite plug and washed with dichloromethane. The filtrate was evaporated to dryness under vacuum to give a clear oil. (Yield: 5.38g, 93%).

Step 5: (3-(2,4-difluorophenyl)pyrrolidin-2-yl)methanol

To a stirred solution of l-ie/t-butyl 2-ethyl 4-(2,4-difluorophenyl)pyrrolidine-l,2-dicarboxylate (5.38 g, 15.14 mmol) and lithium chloride (2.246 g, 53.0 mmol) in a mixture of methanol (38 mL) and tetrahydrofuran (38 mL) was added sodium borohydride (2.005 g, 53.0 mmol) at 0 °C. The thus obtained white suspension was allowed to stir at room temperature overnight. Thereupon, a second crop of lithium chloride (1 g) and sodium borohydride (1 g) was added and the mixture was allowed to stir for additional 48 h. Water was then added, whereupon the organic layer was diluted with dichloromethane, separated, dried over MgS0 ₄ and evaporated to dryness under vacuum. The product was purified by chromatography (petroleum ether - ethyl acetate) and then isolated as a yellow oil. (Yield: 1.96g, 41%).

Step 6: tert-buty -(2,4-difluorophenyl)-2-formylpyrrolidine-l-carboxylate

To a stirred solution of tert-butyl 4-(2,4-difluorophenyl)-2-(hydroxymethyl)pyrrolidine-l- carboxylate (1.96 g, 6.26 mmol) in dichloromethane (78 mL) was added Dess-Martin periodinane (3-oxo-l ⁵ -benzo[<i][l,2]iodaoxole-l,l,l(3H)-triyl triacetate) (2.65 g, 6.26 mmol) at room temperature. The thus obtained pale pink suspension was allowed to stir at room temperature for 4 h. The solvent was then evaporated off under vacuum and the product was purified by chromatography (petroleum ether - ethyl acetate; 1:0, 8: 1, 6:1, 4:1, then 2: 1). The product was isolated as a colourless oil. (Yield: 1.5 g, 90%).

Step 7: 4-(2,4-difluorophen l)pyrrolidine-2-carbaldehyde hydrochloride

A 2 M solution of HCI (19.27 mL, 38.5 mmol) in diethyl ether was added to ie/t-butyl 4-(2,4- difluorophenyl)-2-formylpyrrolidine-l-carboxylate (1.5 g, 4.82 mmol) at room temperature and the yellow solution was allowed to stir at room temperature for 4 h. The solvent was then evaporated off under vacuum to give the product as a yellow oil. (Yield: 1.19 g, 100%).

Step 8: 6-(2,4-dtfluorophenyl)-6, 7-dihydro-2 -thione

To a stirred solution of 4-(2,4-difluorophenyl)pyrrolidine-2-carbaldehyde hydrochloride (1.19 g,

4.80 mmol) in N,N-dimethylformamide (24 mL) was added potassium thiocyanate (0.934 g, 9.61 mmol) at room temperature, whereupon the resulting brown solution was allowed to stir at 100

°C for 90 min. Thereupon, water was added and the organic layer was diluted with diethyl ether containing few drops of ethyl acetate. The organic layer was separated and the aqueous layer was extracted again. The combined organic layers were washed with water (three times), dried over MgSCn and evaporated to dryness under vacuum to give a brown semisolid. Recrystallisation from ethanol afforded the product as a beige solid. (Yield: 0.08g, 6%).

Ή NMR (DMSO-iM): 11.83 (1 H, br s), 7.45 (1 H, td, J = 8.7, 6.7 Hz), 7.28 (1 H, ddd, J = 2.7, 9.4, 11.5 Hz), 7.09 (1 H, dt, J = 2.6, 8.6 Hz), 6.64 (1 H, s), 4.24 (1 H, quin, J = 8.0 Hz), 4.15 (1 H, dd, J = 11.1, 8.1 Hz), 3.72 (1 H, dd, J = 11.3, 7.8 Hz), 3.24 (1 H, dd, J = 8.2, 15.2 Hz), 2.90 (1 H, ddd, J = 15.5, 8.3, 1.5 Hz).

¹³ C NMR (DMSO- 6): 162.3, 162.2, 161.1, 161, 160.6, 160.5, 159.5, 159.4, 156, 132.2, 129.9, 129.8, 129.8, 129.8, 124.3, 124.3, 124.2, 124.2, 111.8, 111.8, 111.7, 111.7, 106.9, 104.3, 104.2, 104.0, 49.3, 40.1, 30.1.

Example 52: 6-(2,5-difluorophenyl)-6,7-diJiydro-2H-pyrrolo[l,2-c]imidazo le-3(5H)-thione

2-(2,5-Difluorophenyl)acetic acid was converted to 6-(2,5-difluorophenyl)-6,7-dihydro-2H- pyrrolo[l,2-c]imidazole-3(5H)-thione by a similar procedure as described for Example 51 and the product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.83 (1 Η, br s), 7.30 (2 Η, m), 7.19 (1 Η, m), 6.65 (1 Η, s), 4.27 (1 Η, quin, J = 8.1 Hz), 4.16 (1 H, dd, J = 11.2, 8.2 Hz), 3.75 (1 H, dd, J = 8.1, 11.2 Hz), 3.24 (1 H, dd, J = 15.5, 8.0 Hz), 2.94 (1 H, br dd, J = 15.3, 8.4 Hz).

¹³ C NMR (DMSO- 6): 159, 157.5, 157.2, 156, 155.6, 132.1, 129.8, 129.7, 129.7, 129.6, 117.2, 117.1, 117.0, 117.0, 115.5, 115.5, 115.4, 115.4, 115.4, 115.3, 115.3, 115.2, 106.9, 49.1, 40.5, 29.9.

Example 53: 5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]p yrrolo[l,2- c]imidazole-3(2H)-thione

Step 1: (2-(aminomethyl)-2-(3,5-difluorophenyl)cyclopropyl)methanol

To a stirred solution of 3,5-difluorophenylacetonitrile (3 g, 19.59 mmol) in dry terahydrofuran (30 mL), was added 2-(chloromethyl)oxirane (1.839 mL, 23.51 mmol) at room temperature, under nitrogen, The reaction was then cooled to 0° C and 2 M sodium bis(trimethylsilyl)amide in terahydrofuran (17.14 mL, 34.3 mmol) was added, dropwise at 0-5 °C. Thereupon, the thus obtained red mixture was allowed to warm up to room temperature and stirred for 3 h. The reaction was diluted with dry terahydrofuran (30 mL), cooled to 0 °C, whereupon sodium borohydride (2.96 g, 78 mmol) was added, followed by dropwise addition of boron trifluoride diethyl etherate (9.93 mL, 78 mmol). The mixture was allowed to warm up to room temperature and stirred overnight. The resulting pale yellow suspension was cooled to 0 °C and carefully quenched with 2 M HC1 (58.8 mL, 118 mmol). The terahydrofuran was then evaporated off and the aqueous phase was washed with diethyl ether. The pH of the aqueous phase was set to pH = 10 by adding 3 M sodium hydroxide and then extracted with dichloro methane. The organic phase was dried over MgSC , filtered and evaporated to dryness under vacuum to leave a yellow oil. (Yield: 3.01 g, 65%).

Step 2: tert-butyl (l-(3,5-difluorophenyl)-2-(hydroxymethyl)cyclopropyl)methylc arbamate

To an ice-cold solution of (2-(aminomethyl)-2-(3,5-difluorophenyl)cyclopropyl)methanol (3 g, 14.07 mmol) in ethanol (32 mL) was added di-ie/t-butyl dicarbonate (3.38 g, 15.48 mmol). The solution was stirred at room temperature for 4 h and then the solvent was evaporated off under vacuum. The resulting yellow oil was purified by chromatography (dichloromethane - methanol). The product was isolated as a pale yellow oil. (Yield: 3.9 g, 88%).

Step 3: tert-butyl l-(3,5-difluorophenyl)-4-hydroxy-3-az bicyclo[3.1.0]hexane-3-carboxylate

To a stirred solution of oxalyl dichloride (1.194 mL, 13.69 mmol) in dry dichloromethane (33 mL), was added dropwise a solution of dimethylsulfoxide (1.945 mL, 27.4 mmol) in dry dichloromethane (6 mL) at -78 °C. The reaction mixture was stirred in the cold for 5 min, and then a solution of tert-butyl (l-(3,5-difluorophenyl)-2-

(hydroxymethyl)cyclopropyl)methylcarbamate (3.9 g, 12.45 mmol) in dry dichloromethane (12 mL) was added dropwise. The mixture was stirred at -78 °C for 45 min and then triethylamine (8.67 mL, 62.2 mmol) was added. The reaction was allowed to warm up gradually to room temperature and stirred at room temperature for 2 h. Thereupon, the mixture was washed three times with water, dried over MgSC , filtered and evaporated to dryness to give a yellow oil. (Yield: 3.96 g, 82%).

Step 4:

To a stirred solution of tert-butyl l-(3,5-difluorophenyl)-4-hydroxy-3-azabicyclo[3.1.0]hexane- 3-carboxylate (3.9 g, 12.53 mmol) in dry dichloromethane (260 mL) was added trimethylsilanecarbonitrile (4.46 mL, 33.4 mmol) at room temperature under nitrogen. The solution was then cooled to -78 °C and boron trifluoride etherate (4.62 mL, 36.7 mmol) was added dropwise. The reaction mixture was stirred in the cold for 4 h. and then saturated solution of sodium bicarbonate was added and the mixture was allowed to warm up to room temperature. The organic phase was separated and aqueous phase was extracted with dichloromethane. The combined organic phases were dried over MgSC , filtered and evaporated to dryness to leave a pinkish oil. (Yield: 3.88 g, 77%).

Step 5: 3-(tert-butoxycarbonyl)-5-(3,5-difluorophenyl)-3-az bicyclo[3.1.0]hexane-2-carboxylic acid

To a stirred solution of tert-butyl 4-cyano-l-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-3- carboxylate (3.6 g, 11.24 mmol) in ethanol (36 mL), was added a solution of 3 M sodium hydroxide (18.73 mL, 56.2 mmol) at room temperature. The solution was heated at 80 °C for 3 h. and then was cooled to room temperature. Thereupon, ethanol was evaporated off and the aqueous phase was acidified with 2 M HCl solution and then extracted with ethyl acetate. The organic phase was dried over MgS0 ₄ , filtered and evaporated to dryness to leave a yellow solid. (Yield: 2.95 g, 66%).

Step 6: tert-butyl 3-tert-butyl 2-methyl 5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-2,3- dicarboxyla

To a stirred solution of 3-(ieri-butoxycarbonyl)-5-(3,5-difluorophenyl)-3- azabicyclo[3.1.0]hexane-2-carboxylic acid (1.8 g, 5.30 mmol) in N,N-dimethylforamide (18 mL) was added potassium carbonate (2.133 g, 15.44 mmol) followed by addition of methyl iodide (1.658 mL, 26.5 mmol). The reaction was stirred at room temperature for 6 h, water was then added and the mixture was extracted with ethyl acetate. The organic phase was dried over MgS0 ₄ , filtered and evaporated to dryness. The thus obtained yellow oil was purified by chromatography (petroleum ether - ethyl acetate). The product was isolated as a pale yellow oil. (Yield: 1.36 g, 69%).

Step 7: tert-butyl l-(3,5-difluorophenyl)-4-(hydroxymethyl)-3-azabicyclo[3.1.0] hexane-3- carboxylate

To a stirred solution of 3-ie/t-butyl 2-methyl 5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane- 2,3-dicarboxylate (1.35 g, 3.82 mmol) in a mixture of methanol (10 mL) and dry tetrahydrofuran (10 mL), was added lithium chloride (0.274 mL, 13.37 mmol) at 0 °C followed by addition of sodium borohydride (0.506 g, 13.37 mmol). The resulting white suspension was allowed to warm up to room temperature and stirred overnight. Water was then added and the mixture was extracted with dichloromethane. The organic phase was dried over MgSCn, filtered and evaporated to dryness to leave the product as a pale yellow oil. (Yield: 1.23 g, 94%).

Step 8: te -butyl l-(3,5-difluorophenyl)-4-formyl-3-az bicyclo[3.1.0]hexane-3-carboxylate

To a stirred solution of tert-butyl l-(3,5-difluorophenyl)-4-(hydroxymethyl)-3- azabicyclo[3.1.0]hexane-3-carboxylate (1.23 g, 3.78 mmol) in dichloromethane (45 mL) was added , Dess-Martin periodinane (3-oxo-l ⁵ -benzo[< J[l,2]iodaoxole-l,l,l(3H)-triyl triacetate) (1.603 g, 3.78 mmol) at room temperature and the reaction was stirred for 24 h. The mixture was then evaporated to small volume and separated by chromatography (petroleum ether - ethyl acetate). The product was isolated as a pale yellow oil. (Yield: 0.96 g, 79%).

Step 9: 5-(3, -difluorophenyl)-3-azabicyclo[3.1.0]hexane-2-carbaldehyde hydrochloride

2 M HCI in diethyl ether (10.64 mL, 21.28 mmol) was added to ieri-butyl l-(3,5- difluorophenyl)-4-formyl-3-azabicyclo[3.1.0]hexane-3-carboxy late (0.86g, 2.66 mmol) to give a colourless solution. The solution was stirred at room temperature for 3 h, whereupon the solvent was evaporated off and the residues was azeotroped with toluene to leave the product as a yellow oil. (Yield: 0.690 g, 90%).

Step 10: 5a-( 3, 5-difluorophenyl)-5, 5a, 6, 6a-tetrahydrocyclopropa[3,4]pyrrolo[l,2-c Jimidazole- 3(2H)-thione

To a stirred solution of 5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-2-carbaldeh yde hydrochloride (690 mg, 2.66 mmol) in N,N-dimethylformamide (13 mL) was added potassium thiocyanate (516 mg, 5.31 mmol), at room temperature, The solution was then heated at 100 °C for 90 min. Thereupon, the mixture was cooled to room temperature, water was added and then extracted with diethyl ether. The organic phase was washed with water, dried over MgSC , filtered and evaporated to dryness to leave a brown oil. Chromatography (dichloro methane - methanol) followed by recrystallization from 2-propanol afforded the product as a beige solid. (Yield: 0.068 g, 8%).

Ή NMR (DMSO-iM): 11.75 (1 H, br s), 7.12 (3 H, m), 6.67 (1 H, s), 4.22 (1 H, d, J = 12.2 Hz), 4.05 (1 H, d, J = 12.2 Hz), 3.00 (1 H, dd, J = 8.3, 4.3 Hz), 1.67 (1 H, dd, J = 8.4, 5.3 Hz), 1.19 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-iM): 163.4, 163.3, 161.8, 161.7, 156.8, 144.8, 144.8, 144.7, 134.5, 110.1, 110.1, 110.0, 109.9, 105.9, 102.3, 102.1, 101.9, 50.6, 36.4, 25.3, 23.0.

Example 54: (5a5,6a ?)-5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione.

3,5-Difluorophenylacetonitrile and ( ?)-2-(chloromethyl)oxirane was converted to (5aS,6a/?)-5a- (3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-ίΜ): 11.75 (1 H, br s), 7.12 (3 H, m), 6.67 (1 H, s), 4.22 (1 H, d, J = 12.2 Hz), 4.05 (1 H, d, J = 12.2 Hz), 3.00 (1 H, dd, J = 8.3, 4.3 Hz), 1.67 (1 H, dd, J = 8.4, 5.3 Hz), 1.19 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-iM): 163.4, 163.3, 161.8, 161.7, 156.8, 144.9, 144.8, 144.7, 134.5, 110.1, 110.1, 110, 109.9, 105.9, 102.3, 102.1, 101.9, 50.6, 36.4, 25.3, 23.0.

5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-

2,5-Difluorophenylacetonitrile and 2-(chloromethyl)oxirane was converted to 5a-(2,5- difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrrolo[l ,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.30 (2 Η, m), 7.21 (1 Η, m), 6.69 (1 Η, s), 4.11 (1 Η, d, J = 12.4 Hz), 3.83 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.66 (1 H, dd, J = 8.4, 5.3 Hz), 1.18 (1 H, m).

¹³ C NMR (DMSO-iM): 158.8, 158.7, 157.2, 157.1, 156.6, 134.5, 128.6, 128.6, 128.5, 128.4, 117.2, 117.1, 117.0, 117.0, 117.0, 116.8, 116.8, 115.9, 115.9, 115.8, 115.7, 106.2, 51.4, 51.4, 32.7, 22.3, 21.0. Example 56: (5a5,6a ?)-5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,5-Difluorophenylacetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5a5,6a/?)-5a- (2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.30 (2 Η, m), 7.21 (1 Η, m), 6.69 (1 Η, d, J = 2 Hz), 4.11 (1 H, d, J = 12.4 Hz), 3.83 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.66 (1 H, dd, J = 8.4, 5.3 Hz), 1.18 (1 H, m).

¹³ C NMR (DMSO-iM): 158.8, 158.7, 157.2, 157.2, 157.1, 157.1, 156.7, 134.5, 128.6, 128.5, 128.5, 128.4, 117.2, 117.1, 117.0, 117.0, 116.9, 116.8, 116.8, 115.9, 115.9, 115.8, 115.7, 106.1. Example 57: (5a ?,6a5)-5a-(2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,5-Difluorophenylacetonitrile and (5)-2-(chloromethyl)oxirane was converted to (5a ?,6a5)-5a- (2,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.30 (2 Η, m), 7.21 (1 Η, m), 6.69 (1 Η, s), 4.11 (1 Η, d, J = 12.4 Hz), 3.83 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.66 (1 H, dd, J = 8.4, 5.3 Hz), 1.18 (l H, m).

¹³ C NMR (DMSC M): 158.8, 158.7, 158.7, 157.2, 157.1, 156.6, 134.5, 128.6, 128.6, 128.5, 128.4, 117.2, 117.1, 117.0, 117.0, 117.0, 116.8, 116.8, 115.9, 115.9, 115.8, 115.7, 106.2, 51.4, 51.4, 32.7, 22.3, 21.0.

Example 58: ( ?)-6-(3,5-difluorophenyl)-6,7-diJiydro-2H-pyrrolo[l,2-c]imid azole-3(5H)-thione Step 1: (E)-l,3-difluoro-5-(2-nitrovinyl)benzene To a solution of methanol (72 mL), water (36 mL), and 2.5 M sodium hydroxide (32.4 mL, 81 mmol) was added a solution of 3,5-difluorobenzaldehyde (10 g, 70.4 mmol) and nitromethane (4.36 mL, 81 mmol) in methanol (12.00 mL) dropwise over 30 min at 5 °C, while the internal temperature was maintained between 5 and 10 °C with external cooling. The reaction was then agitated in the cold for an additional 0.5 h, and then a solution of cc. HC1 (11.73 mL, 141 mmol) in water (36 mL) was added in one portion at 0-10 °C with stirring. The resulting crystals were collected, washed with water and dried to give the product as a light yellow powder. (Yield: 7.0 g, 54%).

Step 2: -diethyl 2-(l-(3,5-difluorophenyl)-2-nitroethyl)malonate

To a stirred solution of (E)-l,3-difluoro-5-(2-nitrovinyl)benzene (7.4 g, 40.0 mmol) in dry tetrahydrofuran (75 mL) was added 4-((5)-hydroxy((15,2 ?,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol (CAS # 70877-75-7) (0.620 g, 1.999 mmol) at room temperature with stirring followed by addition of diethyl malonate (8.65 mL, 56.7 mmol). The mixture was cooled to -5 to -7 °C under inert atmosphere and stirred for 20 h in the cold. Thereupon, the mixture was evaporated to dryness under vacuum and the residue was taken up in dichloromethane (100 mL), washed with 1 M HC1, brine, dried over MgSC and filtered on a silica pad. The filtrate was concentrated to 20 mL, and the residue was crystallized on dilution with petroleum ether (ca. 50 mL). The mixture was further diluted with petroleum ether (120 mL), and aged at 5-10 °C. The resulting solid was collected, washed with petroleum ether, and dried to give the product as an off-white powder. (Yield: 9.1 g, 70%).

Step 3: (4R)-eth -(3,5-difluorophenyl)-2-oxopyrrolidine-3-carboxylate

To a suspension of (7?)-diethyl 2-(l-(3,5-difluorophenyl)-2-nitroethyl)malonate (9 g, 26.1 mmol) in methanol (150 mL) was added nickel(II) chloride hexahydrate (6.20 g, 26.1 mmol) followed by addition of sodium borohydride (7.89 g, 209 mmol) in portions with ice cooling. The mixture was stirred for 6 h at room temperature, then quenched with ammonium chloride solution (250 mL), diluted with dichloromethane (150 mL), acidified with 6 M HC1 to pH=2, and stirred for 16 h. Thereupon, the mixture was extracted with dichloromethane, the organic phase was dried over MgS0 ₄ and evaporated to dryness to give the product as a beige powder. (Yield: 6.87 g, 98%). Step 4: (4R)-4-(3,5-difluorophenyl)-2-oxopyrrolidine-3-carboxylic acid

To a stirred solution of ( K)-ethyl 4-(3,5-difluorophenyl)-2-oxopyrrolidine-3-carboxylate (6.85 g, 25.4 mmol) in ethanol (100 mL) was added 1 M sodium hydroxide (30.5 mL, 30.5 mmol). The resulting suspension was stirred for 1 h, the organics were then removed under vacuum, and the residue was dissolved in water (250 mL). The product was crystallized on acidification with 6 M HC1. The resulting crystals were collected, washed with cold water and dried under vacuum at 50 °C to give the product as a beige powder Yield: 5.2 g, 21, 85%.

Step 5: (R)-4-(3,5-difluorophenyl)pyrrolidin-2-one

A solution of (4 ?)-4-(3,5-difluorophenyl)-2-oxopyrrolidine-3-carboxylic acid (5.2 g, 21.56 mmol) in toluene (300 mL) was stirred under reflux for 3 h, whereupon the mixture was evaporated to dryness, Crystallization from petroleum ether afforded beige powder. Yield: 4.06 g, 96%.

Step 6: (R)-tert-butyl 4-(3,5-difluorophenyl)-2-oxopyrrolidine-l-carboxylate

To a stirred solution of ( ?)-4-(3,5-difluorophenyl)pyrrolidin-2-one (4.05 g, 20.54 mmol) in dry dichloromethane (15 mL) was added at room temperature di-tert- butyl dicarbonate (6.72 g, 30.8 mmol) followed by addition of N,N-dimethylpyridin-4-amine (2.509 g, 20.54 mmol) and triethyl amine (2.86 mL, 20.54 mmol). The mixture was then stirred at room temperature for 3 h, and then concentrated under vacuum. Chromatography (petroleum ether - ethyl acetate; 4: 1) gave an oil which was crystallized from petroleum ether (60 mL), The product was isolated as a white powder. Yield: 6.24 g, 88 %.

Step 7: (4R)-tert-butyl 4-(3,5-difluorophenyl)-2-hydroxypyrrolidine-l-carboxylate

To a stirred solution of {R)-tert-buty\ 4-(3,5-difluorophenyl)-2-oxopyrrolidine-l-carboxylate (2 g, 6.73 mmol) in dry diethyl ether (30 mL) was added dropwise 65% RED-A1 (bis(2- methoxyethoxy)aluminum(III) sodium hydride) (1.212 mL, 4.04 mmol) in toluene at 0-5 °C under nitrogen and the mixture was stirred for 30 min. in the cold. Thereupon, the mixture was quenched with sodium bicarbonate solution and stirred for 30 min. The organic phase was dried over MgS0 ₄ , and evaporated to dryness to give the product as colourless oil. (Yield: 2.07 g, 93%).

Step 8: (4R)-tert-butyl 2-cyano-4-(3,5-difluorophenyl)pyrrolidine-l-carboxylate

To a stirred solution of {AR)-tert-buty\ 4-(3,5-difluorophenyl)-2-hydroxypyrrolidine-l- carboxylate (2 g, 6.68 mmol) in dry dichloromethane (50 mL) was added trimethylsilanecarbonitrile (1.792 mL, 13.36 mmol) followed by addition of boron trifluoride diethyl etherate (1.863 mL, 14.70 mmol) at -70 °C. The mixture was stirred for 4 h in the cold, quenched with sodium bicarbonate solution, and then allowed to warm up with stirring to room temperature. The organic phase was dried over MgSC , filtered and evaporated to dryness under vacuum. Chromatography (petroleum ether - ethyl acetate; 9: 1) afforded the compound as a colourless oil. (Yield: 1.36 g, 66%).

Step 9: (4R)-l-(tert-butoxycarbonyl)-4-(3,5-difluorophenyl)pyrrolidi ne-2-carboxylic acid

To a stirred solution of {AR)-tert-buty\ 2-cyano-4-(3,5-difluorophenyl)pyrrolidine-l-carboxylate (1.35 g, 4.38 mmol) in ethanol (15 mL) was added 3 M sodium hydroxide (7.30 mL, 21.89 mmol) and the solution was gently refluxed (oil bath at 80 °C) for 3 h. Thereupon, ethanol was removed under vacuum and the residue was diluted with water (10 mL), and then acidified with 2 M HC1 to pH = 2 at 10-15 °C. The mixture was extracted with dichloro methane (40 mL), the insoluble materials in both phases was filtered off, whereupon the organic phase was washed with brine, dried over MgSC and evaporated to dryness to give 0.89 g of yellowish oil. (Yield: 62%).

Step 10: (4R)-tert-butyl 4-(3,5-difluorophenyl)-2-(hydroxymethyl)pyrrolidine-l-carbox ylate

To a stirred solution of (4 ?)-l-(ieri-butoxycarbonyl)-4-(3,5-difluorophenyl)pyrrolidine -2- carboxylic acid (0.45 g, 1.375 mmol) in isopropyl acetate (2 mL) was added sodium borohydride (0.083 g, 2.200 mmol) at 0-5 °C followed by addition of boron trifluoride diethyl etherate (0.348 mL, 2.75 mmol. The mixture was stirred for 2 h in the cold, then quenched with 0.5 M sodium hydroxide (9.90 mL, 4.95 mmol), and allowed to stir at room temperature for 30 min. The organic phase was separated, dried over MgSC , evaporated to dryness to leave an oil. Purification by chromatography (petroleum ether - EtOAc; 4: 1, then 2: 1). The product was isolated as a yellowish oil. (Yield: 0.29 g, 67%).

Step 11: (4R)-tert-butyl 4-(3,5-difluorophenyl)-2-formylpyrrolidine-l-carboxylate

To a stirred solution of (4R)-tert-butyl 4-(3,5-difluorophenyl)-2-(hydroxymethyl)pyrrolidine-l- carboxylate (0.28 g, 0.894 mmol) in dry dichloromethane (8 mL) was added Dess-Martin periodinane (3-oxo- ⁵ -benzo[ ][l,2]iodaoxole-l,l,l(3H)-triyl triacetate) (0.379 g, 0.894 mmol) in one portion to give a clear solution. Thereupon, the mixture was stirred at room temperature for 3 h, concentrated to approximately one third and subjected to chromatography (petroleum ether - ethyl acetate 9: 1, then 4: 1). The product was isolated as yellowish oil. (Yield: 0.25 g, 90%).

Step 12: (R)-6-(3 5-dtfluorophenyl)-6, 7-dihydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione

A solution of (4R)-tert-butyl 4-(3,5-difluorophenyl)-2-formylpyrrolidine-l-carboxylate (0.24 g, 0.771 mmol) in 2 M HCl (3.08 mL, 6.17 mmol) in diethyl ether was stirred at room temperature for 16 h. whereupon diethyl ether was evaporated off under reduced pressure, and the residue dissolved in a mixture of ethanol (5 mL) and water (5 mL). Thereupon, potassium thiocyanate (0.082 g, 0.848 mmol) was added followed by addition of cc. HCl (0.032 mL, 0.385 mmol) and the solution was stirred under reflux for 5 h. The mixture was then cooled in ice-water bath, the resulting solid was collected by filtration, washed with water, isopropanol and petroleum ether, and then dried at 50 °C under vacuum to give the product as a beige powder. (Yield: 0.12 g, 62%). Ή NMR (DMSO-ίΜ): 11.81 (1 H, br s), 7.15 (3 H, m), 6.65 (1 H, s), 4.20 (1 H, dd, J = 11.0, 8.1 Hz), 4.13 (1 H, quin, J = 8.3 Hz), 3.72 (1 H, dd, J = 11.2, 8.5 Hz), 3.24 (1 H, ddd, J = 15.3, 7.9, 0.9 Hz), 2.92 (1 H, ddd, J = 15.3, 9.0, 1.8 Hz).

¹³ C NMR (DMSC M): 163.3, 163.2, 161.7, 161.6, 156, 145.5, 145.5, 145.4, 132.3, 110.8, 110.8, 110.7, 110.7, 106.9, 102.7, 102.5, 102.3, 49.9, 46.6, 30.8.

Example 59: (5)-6-(3,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione

(E)-l,3-Difluoro-5-(2-nitrovinyl)benzene (using 4-(( ?)-hydroxy((15,25,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0)) was converted to (5)- 6-(3,5-difluorophenyl)-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-thione by a similar procedure as described for Example 58 and the product was isolated as a dark beige powder Ή NMR (DMSO-iM): 11.81 (1 Η, br s), 7.15 (3 Η, m), 6.65 (1 Η, s), 4.20 (1 Η, dd, J = 11.0, 8.1 Hz), 4.13 (1 H, quin, J = 8.3 Hz), 3.72 (1 H, dd, J = 11.2, 8.5 Hz), 3.24 (1 H, ddd, J = 15.3, 7.9, 0.9 Hz), 2.92 (1 H, ddd, J = 15.3, 9.0, 1.8 Hz).

¹³ C NMR (DMSC M): 163.3, 163.2, 161.7, 161.6, 156, 145.5, 145.5, 145.4, 132.3, 110.9, 110.8, 110.7, 110.7, 106.9, 102.7, 102.5, 102.4, 49.9, 46.6, 30.8.

Example 60: (5a5,6a ?)-5a-(3,5-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[2,l- c][l,2,4]triazole-3(2H)-thione

Step 1: ( -tert-butyl l-(3, 5-difluorophenyl)-4-oxo-3-azabicyclo[3.1.0 ]hexane-3-carboxylate

To an ice-cooled stirred solution of chromium (VI) oxide (2.137 g, 21.37 mmol) in water (3.77 mL) was added dropwise sulfuric acid (1.125 mL, 21.10 mmol). Thereupon, the obtained orange solution was added dropwise to an ice-cooled solution of tert-butyl (((lS,2 ?)-l-(3,5- difluorophenyl)-2-(hydroxymethyl)cyclopropyl)methyl)carbamat e (2.85 g, 9.10 mmol) in acetone (57 mL) (prepared according to step 1-3 of Example 53 from 2-(3,5- difluorophenyl)acetonitrile and ( ?)-2-(chloromethyl)oxirane). The reaction was stirred in the cold for 1 h, and then 25 mL of isopropanol was added, followed by addition of water. The thus obtained dark aqueous phase was extracted with dichloromethane, whereupon the organic phase was washed with water and evaporated to dryness to give the product as a semi-solid mass. Trituration with disopropyl ether afforded the product as a white powder. (Yield: 1.813 g, 64%). Step 2: (lR,5S)- -(3, 5-difluorophenyl ) -3-azabicyclo[3.1.0 ]hexan-2 -one

To a stirred solution of {\S,5R)-tert-buty\ l-(3,5-difluorophenyl)-4-oxo-3- azabicyclo[3.1.0]hexane-3-carboxylate (1.8 g, 5.82 mmol) in dichloromethane (50 mL) was added 2,2,2-trifluoroacetic acid (3.59 mL, 46.6 mmol) dropwise. The reaction was allowed stir at room temperature for 2 h. Thereupon, the solvent was removed under vacuum, the residue was dissolved in dichloromethane, washed with potassium carbonate solution and evaporated to dryness to leave an off-white crystalline product. Trituration with diethyl ether afforded white crystals. (Yield: 1.135 g, 93%).

Step 3: (lS,5 -l-(3,5-difluorophenyl)-4-methoxy-3-az bicyclo[3.1.0]hex-3-ene

To a stirred solution of (1 ?,55)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexan-2-one (1.0 g, 4.78 mmol) in dry dichloromethane (24 mL) was added trimethyloxonium tetrafluoroborate (0.714 g, 4.83 mmol) under inert atmosphere and the solution was stirred at room temperature for 5 h. The thus obtained turbid solution was treated with saturated aqueous sodium bicarbonate, whereupon the organic phase was washed again with sodium bicarbonate, dried over MgS0 ₄ , filtered and evaporated to dryness to give the product as a colourless oil. (Yield: 1.07 g, 95%).

Step 4: methyl 2-((lR,5S)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hex-2-e n-2- yl)hydrazinecarbodithioate

To a stirred solution of (15,5 ?)-l-(3,5-difluorophenyl)-4-methoxy-3-azabicyclo[3.1.0]hex-3 -ene (1.07 g, 4.79 mmol) in methanol (10 mL) was added methyl hydrazinecarbodithioate (0.586 g, 4.79 mmol) in portions. The solution was stirred at room temperature for 1 h, and then evaporated to dryness to leave a colourless foam. (Yield: 1.5 g, 90%).

Step 5: methyl (5aS,6aR)-5a-(3,5-dtfluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[2,l-c][l,2,4]triazole-3(2H) -thione

A stirred solution of methyl 2-((1 ?,55)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hex-2-en-2- yl)hydrazinecarbodithioate (1.5 g, 4.79 mmol) in N,N-dimethylformamide (25 mL) was heated at reflux under inert atmosphere for 1 h. The mixture was then cooled to room temperature, poured onto ice and stirred for 30 min. The resulting precipitate was filtered off, the filter cake was washed with water and dissolved in ethyl acetate. The organic phase was washed with water again, dried over MgS0 ₄ , filtered and evaporated to dryness. Chromatography (dichloro methane - methanol; 98:2) followed by trituration with a mixture of petroleum ether - diethyl ether afforded the product as an off-white solid. (Yield: 0.104 g, 7%).

Ή NMR (DMSO-iM): 13.19 (1 H, br s), 7.20 (2 H, m), 7.15 (1 H, tt, J = 2.3, 9.3 Hz), 4.25 (1 H, dd, J = 11.9, 0.7 Hz), 4.09 (1 H, d, J = 11.9 Hz), 3.13 (1 H, ddd, J = 0.8, 4.4, 8.7 Hz), 1.80 (1 H, dd, J = 8.7, 5.6 Hz), 1.47 (1 H, dd, J = 5.6, 4.3 Hz). ¹³ C NMR (DMSC M): 163.7, 163.3, 163.2, 161.7, 161.6, 157.9, 143.6, 143.6, 143.5, 110.6, 110.6, 110.5, 110.4, 102.7, 102.5, 102.4, 49.1, 36.9, 23.0, 21.0.

Example 61: (5)-6-(2,3,5,6-tetrafluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2 -c]imidazole-3(5H)- thione

(E)- l,2,4,5-terafluoro-5-(2-nitrovinyl)benzene (using 4-(( ?)-hydroxy((15,25,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0)) was converted to (5)- 6-(2,3,5,6-tetrafluorophenyl)-6,7-diJiydro-2H-pyrrolo[l,2-c] imidazole-3(5H)-thione by a similar procedure as described for Example 59 and the product was isolated as a dark beige powder.

Ή NMR (DMSO-iM): 11.86 (1 Η, br s), 7.86 (1 Η, m), 6.64 (1 Η, s), 4.54 (1 Η, quin, J = 8.5 Hz), 4.20 (1 H, dd, J = 11.6, 9.2 Hz), 3.79 (1 H, dd, J = 11.7, 7.6 Hz), 3.33 (1 H, m), 2.97 (1 H, dd, J = 16.0, 7.6 Hz).

¹³ C NMR (DMSO-iM): 155.9, 146.3, 145.3, 144.7, 143.6, 132.0, 120.5, 120.4, 120.3, 106.7, 105.9, 105.7, 105.6, 48.4, 35.8, 29.4.

Example 62: ( ?)-6-(2,3,5,6-tetrafluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2- c]imidazole-3(5H)- thione

(E)- l,2,4,5-terafluoro-5-(2-nitrovinyl)benzene (using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7)) was converted to ( ?)-6-(2,3,5,6-tetrafluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2- c]imidazole-3(5H)-tM by a similar procedure as described for Example 58 and the product was isolated as a beige powder. Ή NMR (DMSO-iM): 11.86 (1 Η, br s), 7.85 (1 Η, tt, J = 10.4, 7.6 Hz), 6.64 (1 H, m), 4.54 (1 H, m), 4.20 (1 H, dd, J = 11.7, 9.2 Hz), 3.79 (1 H, dd, J = 11.7, 7.6 Hz), 3.33 (1 H, m), 2.97 (1 H, ddd, J = 1.2, 8.0, 16 Hz).

¹³ C NMR (DMSO-iM): 155.9, 146.4, 146.3, 146.3, 145.3, 145.2, 144.8, 144.7, 144.6, 143.7, 143.6, 132, 120.5, 106.7, 105.9, 105.7, 105.6, 48.4, 35.8, 29.4.

Example 63: (5aS,6a7?)-5a-(2,3,5-trifluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

2,3,5-Trifluorophenylacetonitrile and ( ?)-2-(chloromethyl)oxirane was converted to (5aS,6a ?)- 5a-(2,3,5-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole-3(2H)- thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid.

Ή NMR (DMSO- 6): 11.78 (1 Η, br s), 7.50 (1 Η, m), 7.19 (1 Η, m), 6.70 (1 Η, d, J = 2.1 Hz), 4.12 (1 H, d, J = 12.0 Hz), 3.88 (1 H, d, J = 12.0 Hz), 2.95 (1 H, dd, J = 8.5, 4.3 Hz), 1.67 (1 H, dd, J = 8.4, 5.5 Hz), 1.22 (1 H, m).

¹³ C NMR (DMSC M): 157.8, 157.8, 156.7, 156.2, 156.2, 150.5, 150.4, 150.3, 148.9, 148.8, 148.7, 147.3, 147.2, 147.2, 147.2, 145.7, 145.6, 145.6, 145.5, 134.3, 130.2, 130.1, 130.0, 112.3, 112.2, 106.3, 105.3, 105.2, 105.1, 105.0, 51.2, 51.2, 32.6, 32.5, 22.5, 21.1.

Example 64: (5a5,6a ?)-5a-(2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,6-Difluorophenylacetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5aS,6a/?)-5a- (2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclo^

by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.78 (1 H, br s), 7.43 (1 H, m), 7.13 (2 H, m), 6.70 (1 H, s), 4.05 (1 H, d, J = 12.2 Hz), 3.70 (1 H, d, J = 12.2 Hz), 2.71 (1 H, dd, J = 8.3, 4.3 Hz), 1.65 (1 H, dd, J = 8.2, 5.6 Hz), 1.28 (1 H, t, J = 4.9 Hz).

¹³ C NMR (DMSO- 6): 162.7, 162.6, 161, 161, 156.6, 134.6, 130.5, 130.4, 130.3, 115.2, 115.1, 115.0, 112, 112.0, 111.8, 111.8, 106.4, 51.6, 26.4, 21.7, 21.4.

Example 65: (5a ?,6a5)-5a-(2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,6-Difluorophenylacetonitrile and (5)-2-(chloromethyl)oxirane was converted to (5a ?,6a5)-5a- (2,6-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.78 (1 Η, br s), 7.43 (1 Η, m), 7.13 (2 Η, m), 6.70 (1 Η, s), 4.05 (1 Η, d, J = 12.2 Hz), 3.70 (1 H, d, J = 12.2 Hz), 2.71 (1 H, dd, J = 8.3, 4.3 Hz), 1.65 (1 H, dd, J = 8.2, 5.6 Hz), 1.28 (1 H, t, J = 4.9 Hz).

¹³ C NMR (DMSO- 6): 162.7, 162.6, 161, 161, 156.6, 134.6, 130.5, 130.4, 130.3, 115.2, 115.1, 115, 112, 112, 111.9, 111.8, 106.4, 51.6, 26.4, 21.7, 21.4.

Example 66: (5a5,6a ?)-5a-(2,3-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,3-Difluorophenylacetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5a5,6a/?)-5a- (2,3-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a light yellow solid.

Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.39 (1 Η, m), 7.23 (1 Η, m), 7.20 (1 Η, m), 6.70 (1 Η, d, J = 2.2 Hz), 4.12 (1 H, d, J = 12.2 Hz), 3.85 (1 H, d, J = 12.2 Hz), 2.87 (1 H, dd, J = 8.4, 4.3 Hz), 1.65 (1 H, dd, J = 8.4, 5.4 Hz), 1.21 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 156.7, 150.7, 150.6, 150.4, 150.3, 149, 148.9, 148.7, 148.6, 134.5, 129.1, 129.1, 125.6, 124.9, 124.9, 124.9, 124.8, 116.9, 116.8, 106.2, 51.5, 51.5, 32.5, 32.5, 22.1, 20.9.

Example 67: (5a ?,6a5)-5a-(2,3-difluorophenyl)-5,5a,6,6a-tetrahydrocycloprop a[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,3-Difluorophenylacetonitrile and (5)-2-(chloromethyl)oxirane was converted to (5a ?,6a5)-5a- (2,3-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.39 (1 Η, m), 7.23 (1 Η, m), 7.20 (1 Η, m), 6.70 (1 Η, d, J = 2.2 Hz), 4.12 (1 H, d, J = 12.2 Hz), 3.85 (1 H, d, J = 12.2 Hz), 2.87 (1 H, dd, J = 8.4, 4.3 Hz), 1.65 (1 H, dd, J = 8.4, 5.4 Hz), 1.21 (1 H, t, J = 4.8 Hz). ¹³ C NMR (DMSO-J6): 156.7, 150.6, 150.6, 150.4, 150.3, 149, 148.9, 148.7, 148.6, 134.5, 129.1, 129.1, 125.6, 124.9, 124.8, 124.8, 124.8, 116.9, 116.7, 106.2, 51.5, 51.5, 32.5, 32.4, 22.1, 20.9.

Example 68: (5a»S ^, ,6a ?)-5a-(2,3,6-trifluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[ -c]imidazole-3(2H)-thione

2,3,6-Trifluorophenylacetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5a5,6a ?)- 5a-(2,3,6-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole-3(2H)- thione by a similar procedure as described for Example 53 and the product was isolated as a light beige solid.

Ή NMR (DMSO-iM): 11.79 (1 Η, br s), 7.50 (1 Η, m, J = 9.4, 5.0 Hz), 7.17 (1 H, m), 6.71 (1 H, d, J = 2.2 Hz), 4.06 (1 H, d, J = 12.2 Hz), 3.76 (1 H, d, J = 12.2 Hz), 2.77 (1 H, dd, J = 8.3, 4.3 Hz), 1.69 (1 H, dd, J = 8.2, 5.6 Hz), 1.31 (1 H, t, J = 5.0 Hz).

¹³ C NMR (DMSC M): 158.1, 158.1, 156.6, 156.5, 156.5, 150.2, 150.2, 150.1, 150.1, 148.6, 148.5, 148.5, 148.4, 147.4, 147.3, 145.8, 145.7, 134.3, 117.2, 117.2, 117.2, 117.1, 117.1, 117.1, 117.0, 117.0, 111.7, 111.6, 111.6, 111.6, 111.5, 111.5, 111.5, 111.4, 106.5, 51.4, 26.5, 21.5, 21.3.

Example 69: (5a/?,6aS)-5a-(2,3,6-trifluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l -c]imidazole-3(2H)-thione

2,3,6-Trifluorophenylacetonitrile and (S)-2-(chloromethyl)oxirane was converted to (5a ?,6a5)- 5a-(2,3,6-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole-3(2H)- thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.79 (1 Η, br s), 7.50 (1 Η, m, J = 9.4, 5.0 Hz), 7.17 (1 H, m), 6.71 (1 H, d, J = 2.2 Hz), 4.06 (1 H, d, J = 12.2 Hz), 3.76 (1 H, d, J = 12.2 Hz), 2.77 (1 H, dd, J = 8.3, 4.3 Hz), 1.69 (1 H, dd, J = 8.2, 5.6 Hz), 1.31 (1 H, t, J = 5.0 Hz).

¹³ C NMR (DMSC M): 158.1, 156.6, 156.5, 150.2, 150.2, 150.1, 150.1, 148.6, 148.5, 148.5, 148.4, 147.3, 147.3, 145.8, 145.6, 134.3, 117.2, 117.2, 117.1, 117.1, 117.0, 117.0, 117.0, 111.6, 111.4, 106.5, 51.3, 26.5, 21.5, 21.3.

Example 70: (5a5,6a ?)-5a-(2,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione

2,4-Difluorophenylacetonitrile and ( ?)-2-(chloromethyl)oxirane was converted to (5a5,6a/?)-5a- (2,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.47 (1 Η, td, J = 8.7, 6.6 Hz), 7.29 (1 H, ddd, J = 10.9, 9.2, 2.6 Hz), 7.08 (1 H, tdd, J = 1.0, 2.8, 8.6 Hz), 6.68 (1 H, d, J = 2.2 Hz), 4.08 (1 H, d, J = 12.0 Hz), 3.77 (1 H, d, J = 12.2 Hz), 2.77 (1 H, dd, J = 8.3, 4.2 Hz), 1.62 (1 H, dd, J = 8.3, 5.4 Hz), 1.15 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO- 6): 162.7, 162.6, 162.6, 162.6, 161.1, 161, 161, 160.9, 156.6, 134.7, 131.8, 131.8, 131.8, 131.7, 123.1, 123, 123, 122.9, 111.6, 111.5, 111.4, 111.4, 106.1, 104.4, 104.2, 104, 51.7, 32.2, 21.8, 20.7.

Example 71: (5a5,6a ?)-5a-(3,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2- c]imidazole-3(2H)-thione

3,4-Difluorophenylacetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5a5,6a/?)-5a- (3,4-difluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3,4]pyrr olo[l,2-c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid. Ή NMR (DMSO-iM): 11.74 (1 Η, br s), 7.48 (1 Η, ddd, J = 12.1, 7.7, 2.1 Hz), 7.39 (1 H, dt, J = 10.5, 8.7 Hz), 7.21 (1 H, m), 6.66 (1 H, s), 4.20 (1 H, d, J = 12.2 Hz), 3.99 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.64 (1 H, dd, J = 8.2, 5.3 Hz), 1.13 (1 H, t, J = 4.8 Hz) .

1 ³ C NMR (DMSO-iM): 156.7, 150.2, 150.1, 149.2, 149.1, 148.6, 148.5, 147.6, 147.5, 137.9, 137.9, 137.8, 137.8, 134.8, 123.9, 123.9, 123.8, 123.8, 117.5, 117.4, 116.4, 116.3, 105.9, 51.2, 36.1, 24.4.

Example 72: (5a»S ^, ,6a ?)-5a-(2,4,5-trifluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

2,4,5-Trifluorophenylacetonitrile and ( ?)-2-(chloromethyl)oxirane was converted to (5aS,6a ?)- 5a-(2,4,5-trifluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[3, 4]pyrrolo[l,2-c]imidazole-3(2H)- thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.59 (2 Η, m), 6.69 (1 Η, d, J = 2.1 Hz), 4.08 (1 H, d, J = 12.0 Hz), 3.81 (1 H, d, J = 12.0 Hz), 2.86 (1 H, dd, J = 8.3, 4.2 Hz), 1.65 (1 H, dd, J = 8.4, 5.4 Hz), 1.17 (1 H, t, J = 4.8 Hz). ¹³ C NMR (DMSC M): 157.9, 157.8, 156.6, 156.2, 156.2, 149.5, 149.4, 149.4, 147.9, 147.8, 147.7, 146.6, 146.6, 145.0, 145.0, 134.5, 123.8, 123.8, 123.8, 123.7, 118.7, 118.7, 118.6, 118.6, 106.4, 106.3, 106.2, 106.1, 51.5, 51.4, 32.2, 22.2, 21.0. Example 73: (5aS,6a ?)-5a-(3-chloro-5-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

2-(3-Chloro-5-fluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane was converted to (5a5,6a ?)-5a-(3-chloro-5-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.74 (1 Η, br s), 7.31 (2 Η, m), 7.26 (1 Η, ddd, J = 1.7, 2.2, 10.1 Hz), 6.67 (1 H, d, J = 2.2 Hz), 4.23 (1 H, d, J = 12.2 Hz), 4.04 (1 H, d, J = 12.0 Hz), 3.01 (1 H, dd, J = 8.4, 4.3 Hz), 1.67 (1 H, dd, J = 8.4, 5.3 Hz), 1.17 (1 H, dd, J = 4.4, 5.2 Hz).

1 ³ C NMR (DMSO-iM): 163.1, 161.4, 156.8, 144.8, 144.7, 134.5, 134.2, 134.1, 123.1, 123.1, 114.3, 114.2, 113, 112.8, 105.9, 50.7, 36.3, 36.3, 25.1, 22.8.

Example 74: (5a5 ^, ,6a ?)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

2-(5-Chloro-2-fluorophenyl)acetonitrile and ( ?)-2-(chloromethyl)oxirane was converted (5a5,6a ?)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a light yellow solid.

Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.49 (1 Η, dd, J = 6.5, 2.7 Hz), 7.43 (1 H, ddd, J = 8.7, 4.3, 2.8 Hz), 7.30 (1 H, dd, J = 9.9, 8.9 Hz), 6.69 (1 H, s), 4.10 (1 H, d, J = 12.0 Hz), 3.81 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.67 (1 H, dd, J = 8.4, 5.4 Hz), 1.17 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 161.3, 159.7, 156.6, 134.6, 130.2, 130.1, 129.4, 129.3, 128.8, 128.7, 128.3, 128.3, 117.6, 117.4, 106.2, 51.5, 51.5, 32.6, 22.1, 20.9. Example 75: (5a»S ^, ,6a ?)-5a-(2-chloro-5-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

2-(2-Chloro-5-fluorophenyl)acetonitrile and ( ?)-2-(chloromethyl)oxirane was converted to (5a5,6a ?)-5a-(2-chloro-5-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopro pa[3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione by a similar procedure as described for Example 53 and the product was isolated as a light yellow solid.

Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.56 (1 Η, dd, J = 8.8, 5.1 Hz), 7.39 (1 H, dd, J = 9.2, 3.1 Hz), 7.24 (1 H, td, J = 8.5, 3.1 Hz), 6.69 (1 H, d, J = 2.2 Hz), 4.08 (1 H, d, J = 12.2 Hz), 3.76 (1 H, d, J = 12.0 Hz), 2.77 (1 H, dd, J = 8.4, 4.3 Hz), 1.69 (1 H, dd, J = 8.4, 5.4 Hz), 1.20 (1 H, dd, J = 5.3, 4.4 Hz).

¹³ C NMR (DMSC M): 161.5, 159.9, 156.5, 139.2, 139.1, 134.9, 131.2, 131.2, 130.4, 130.4, 118.9, 118.8, 116.6, 116.4, 106.2, 51.2, 36.4, 22.1, 21.8.

Example 76: (5aS,6a/?)-5a-(3,5-difluorophenyl)-2-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

Step 1: (5aS,6aR)-5a-(3,5-difluorophenyl)-l-hydroxy-2- methylhexahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)- thione

To a solution of (1 ?,55)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-2-car baldehyde hydrochloride (analogous to Example 53 step 10) (0,460 g, 1,771 mmol) in dichloromethane (4.4 mL) was added isothiocyanatomethane (0,155 g, 2,126 mmol) and triethylamine (0,299 mL, 2,126 mmol). The reaction mixture was stirred at room temperature for 24 h. Thereupon, the mixture was quenched with water and extracted with dichloromethane. The organic phase was dried over MgSC , filtered and evaporated to dryness. Chromatography (ethyl acetate - petroleum ether; 1:6) afforded the product as a brown solid. (Yield: 0.129 g, 29%).

Step 2: (5aS,6aR)-5a-(3,5-dtfluorophenyl)-2-methyl-5,5a,6,6a- tetrahydrocyclopro a[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thione

To a stirred solution of (5aS,6a ?)-5a-(3,5-difluorophenyl)- 1 -hydro xy-2- methylhexahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)- thione) (0,095 g, 0,321 mmol) in a mixture of ethanol (0,801 mL) and water (0,801 mL) was added 6 M HCI (0,107 mL, 0,641 mmol). The reaction mixture was heated at reflux for 2 h. Thereupon, the mixture was cooled down to room temperature, and ethanol was removed under vacuum. The residue was extracted with dichloromethane, whereupon the organic phase was dried over MgSC , filtrated, concentrated under reduced pressure to give a brown solid which was purified by chromatography (ethyl acetate - petroleum ether; 1: 1). The product was isolated as brown solid. (Yield: 0.067 g, 54%).

Ή NMR (CDCls): 6.78 (2 H, m), 6.74 (1 H, m), 6.44 (1 H, s), 4.31 (1 H, d, J = 12.2 Hz), 4.20 (1

H, d, J = 12.3 Hz), 3.57 (3 H, s), 2.62 (1 H, dd, J = 8.3, 4.0 Hz), 1.69 (1 H, dd, J = 8.2, 5.6 Hz),

I.18 (1 H, dd, J = 5.4, 4.3 Hz). ¹³ C NMR (CDCls): 164.1, 164, 162.4, 162.3, 158, 143.3, 143.2, 143.1, 133.3, 110.3, 110.2, 110.1, 110.1, 109.7, 103.1, 103, 102.8, 52.7, 36.2, 34.8, 24.2, 23.2.

Example 77: (5aS,6a ?)-2-cyclopropyl-5a-(3,5-difluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]p

(1 ?,55)-5-(3,5-Difluorophenyl)-3-azabicyclo[3.1.0]hexane-2-car baldehyde hydrochloride was converted to (5aS,6a ?)-2-cyclopropyl-5a-(3,5-difluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e by a similar procedure as described for Example 76 and the product was isolated as a brown solid.

Ή NMR (DMSO-iM): 7.12 (3 Η, m), 6.79 (1 Η, s), 4.25 (1 Η, d, J = 12.2 Hz), 4.08 (1 H, d, J = 12.2 Hz), 3.37 (1 H, m), 3.00 (1 H, dd, J = 8.4, 4.3 Hz), 1.68 (1 H, dd, J = 8.4, 5.3 Hz), 1.20 (1 H, t, J = 4.8 Hz), 0.93 (2 H, m), 0.86 (2 H, m).

¹³ C NMR (DMSO-iM): 163.4, 163.3, 161.7, 161.7, 158.7, 144.7, 144.6, 144.6, 132.8, 110.2, 110.2, 110.1, 110.0, 107.6, 102.3, 102.2, 102.0, 51.4, 35.8, 35.8, 29.5, 25.1, 23.0, 6.4, 6.4.

Example 78: (5a5,6a/?)-5a-(2,5-difluorophenyl)-l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 80 from (5S)-3-(tert- butoxycarbonyl)-5-(2,5-difluorophenyl)-3-azabicyclo[3.1.0]he xane-2-carboxylic acid and methylmagnesium iodide and isolated as a yellow solid.

Ή NMR (DMSO- 6): 11.66 (1 H, br s), 7.28 (2 H, m), 7.20 (1 H, m), 4.06 (1 H, d, J = 12.0 Hz), 3.78 (1 H, d, J = 12.0 Hz), 2.86 (1 H, dd, J = 8.2, 4.3 Hz), 2.09 (1 H, m), 2.04 (3 H, s), 1.63 (1 H, dd, J = 8.1, 5.4 Hz), 1.13 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-iM): 158.8, 158.7, 157.2, 157.1, 155.7, 130.3, 128.8, 128.8, 128.8, 128.7, 128.6, 117.2, 117.1, 117.0, 116.9, 116.8, 115.9, 115.8, 115.7, 115.7, 114.8, 51.5, 32.5, 22.4, 20.3, 9.4.

Example 79: (5a5,6a/?)-5a-(3,5-difluorophenyl)- l-methyl-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrolo -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 80 from (5S)-3-(tert- butoxycarbonyl)-5-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]he xane-2-carboxylic acid and methylmagnesium iodide and isolated as a yellow solid.

Ή NMR (DMSO-iM): 1.63 (1 Η, br s), 7.10 (3 Η, m), 4.17 (1 Η, d, J = 12.0 Hz), 4.00 (1 H, d, J = 12.2 Hz), 2.97 (1 H, dd, J = 8.3, 4.3 Hz), 2.03 (3 H, s), 1.65 (1 H, dd, J = 8.2, 5.1 Hz), 1.15 (1 H, m).

1 ³ C NMR (DMSC M): 163.4, 163.3, 161.8, 161.7, 156, 145, 130.2, 114.5, 110, 110, 109.9, 109.9, 102.1, 50.7, 36.1, 25.4, 22.4, 9.4.

Example 80: (5)- l-butyl-6-(3,5-difluorophenyl)-6,7-dihydro-2H-pyrrolo[l,2-c] imidazole-3(5H)- thione Step 1: (4S)-tert-butyl 4-(3,5-difluorophenyl)-2-(methoxy(methyl)carbamoyl)pyrrolidi ne-l- carboxylate

To a solution of (4S)-l-(tert-butoxycarbonyl)-4-(3,5-difluorophenyl)pyrrolidi ne-2-carboxylic acid (analogous to Example 58 step 9) (0.982 g, 3 mmol) in dry dichloromethane (10 mL) was added di(lH-imidazol-l-yl)methanone (0.584 g, 3.60 mmol) in portions at room temperature and the mixture was stirred for 30 min. Thereupon, N,0-dimethylhydroxylamine hydrochloride (0.351 g, 3.60 mmol) was added and the stirring was continued at room temperature for 40 h. The reaction was then washed with water, the organic phase was dried over MgS0 ₄ and concentrated under vacuum. Chromatography (petroleum ether - ethyl acetate; 2: 1) afforded the product as an off-white solid. (Yield: 0.92 g, 83%).

Step 2: tert-butyl (4S)-4-(3,5-difluorophenyl)-2-pentanoylpyrrolidine-l-carboxy late

To a solution of (4S)-ie/t-butyl 4-(3,5-difluorophenyl)-2- (methoxy(methyl)carbamoyl)pyrrolidine-l-carboxylate (0.40 g, 1.08 mmol) in dry tetrahydrofuran (2 mL) was added 2 M butylmagnesium bromide (1.62 mL, 3.24 mmol) at 0-5 °C under nitrogen. The mixture was allowed to warm up to room temperature and stirred for 3 h. Thereupon, the mixture was poured onto 1 M HCl and then extracted with diethyl ether. The organic phase was washed with brine, dried over MgS0 ₄ , and evaporated to dryness. Chromatography (petroleum ether - ethyl acetate; 9: 1) afforded the product as a colourless oil. (Yield: 0.2 g, 50%).

Step 3: (S)-l -benzyl-6-( 3,5-difluorophenyl)-6, 7-dihydro-2H-pyrrolo[l,2-c ]imidazole-3( 5H)- thione

A mixture of (45)-tert-butyl 4-(3,5-difluorophenyl)-2-pentanoylpyrrolidine-l-carboxylate (0.19 g, 0.517 mmol) and 4 M HCI (2.59 mL, 10.34 mmol) in dioxane was stirred at room temperature overnight. The mixture was then cooled to room temperature and evaporated to dryness. The thus obtained oily residue was dissolved in a mixture of ethanol (2 mL) and water (2 mL), followed by addition of potassium thiocyanate (0.055 g, 0.569 mmol) and 6 M HCI (0.043 mL, 0.259 mmol). The mixture was stirred under reflux for 1 h, then stirred at room temperature for 30 min. The obtained solid was collected by filtration, washed with a mixture of ethanol water (1: 1) and dried under vacuum at 50 °C to give the product as a light beige powder. (Yield: 0.12 g, 75%).

Ή NMR (DMSO- 6): 11.71 (1 H, s), 7.13 (3 H, m), 4.14 (1 H, dd, J = 11.2, 7.9 Hz), 4.07 (1 H, quin, J = 8.1 Hz), 3.67 (1 H, dd, J = 11.1, 8.3 Hz), 3.20 (1 H, dd, J = 15.0, 7.8 Hz), 2.84 (1 H, dd, J = 15.1, 8.8 Hz), 2.35 (2 H, t, J = 7.5 Hz), 1.50 (2 H, m), 1.26 (2 H, m), 0.86 (3 H, t, J = 7.4 Hz). ¹³ C NMR (DMSO-iM): 163.3, 163.2, 161.7, 161.6, 155.1, 145.8, 145.7, 145.6, 127.6, 120, 110.8, 110.7, 110.6, 110.6, 102.6, 102.5, 102.3, 49.9, 46.5, 30.4, 29.8, 23.6, 21.5, 13.6.

Example 81: 6-cyclohexyl-6,7-dihydro-2H-pyrrolo[l,2-c]imidazole-3(5H)-th ione

Compound was prepared in an analogous manner to Example 58 from diethyl 2-(l-cyclohexyl-2- nitroethyl)malonate (Liu, Jin-ming; Wang, Xin; Ge, Ze-mei; Sun, Qi; Cheng, Tie-ming; Li, Run- tao Tetrahedron (2011), 67(3), 636-640) and isolated as a beige powder. Ή NMR (DMSO-ίΜ): 11.68 (1 H, br s), 6.52 (1 H, s), 3.84 (1 H, dd, J = 11.3, 7.9 Hz), 3.33 (1 H, dd, J = 9.0, 11.5 Hz), 2.86 (1 H, ddd, J = 0.8, 7.8, 15.1 Hz), 2.57 (1 H, m), 2.47 (1 H, m), 1.65 (5 H, m), 1.43 (1 H, m), 1.18 (3 H, m), 0.96 (2 H, m).

¹³ C NMR (DMSC M): 155.6, 133.2, 106.3, 48.4, 47.8, 41, 30.7, 30.4, 27.5, 25.9, 25.5.

Example 82: (5)-6-(2,3,5-trifluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3- thione

Compound was prepared in an analogous manner to Example 59 from (E)-l,2,5-trifluoro-3-(2- nitro vinyl)benzene using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst CAS # 524-63-0) and isolated as a beige powder.

Ή NMR (DMSO-iM): 11.84 (1 Η, br s), 7.48 (1 Η, m), 7.21 (1 Η, m), 6.65 (1 Η, m), 4.33 (1 Η, quin, J = 8.2 Hz), 4.17 (1 H, dd, J = 11.3, 8.1 Hz), 3.77 (1 H, dd, J = 11.4, 8.1 Hz), 3.26 (1 H, ddd, J = 15.4, 8.2, 0.9 Hz), 2.94 (1 H, ddd, J = 15.4, 8.5, 1.5 Hz).

1 ³ C NMR (DMSC M): 158.1, 158.1, 158.0, 158.0, 156.5, 156.5, 156.4, 156.4, 156.1, 150.6,

150.5, 150.4, 148.9, 148.8, 148.7, 145.7, 145.7, 145.6, 145.6, 144.1, 144.1, 144.0, 144.0, 131.9,

131.5, 131.4, 131.4, 131.3, 110.7, 110.5, 107.0, 104.9, 104.7, 104.7, 104.5, 49.0, 40.3, 30.0.

Example 83: ( ?)-6-(2,3,5-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[l ,2-c]imidazole-3- thione

Compound was prepared in an analogous manner to Example 58 from (E)-l,2,5-trifluoro-3-(2- nitrovinyl)benzene using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7) and isolated as a beige powder.

Ή NMR (DMSO-iM): 11.84 (1 H, br s), 7.48 (1 H, m), 7.21 (1 H, m), 6.65 (1 H, m), 4.33 (1 H, quin, J = 8.2 Hz), 4.17 (1 H, dd, J = 11.3, 8.1 Hz), 3.77 (1 H, dd, J = 11.4, 8.1 Hz), 3.26 (1 H, ddd, J = 15.4, 8.2, 0.9 Hz), 2.94 (1 H, ddd, J = 15.4, 8.5, 1.5 Hz).

¹³ C NMR (DMSC M): 158.1, 158.1, 158.0, 158.0, 156.5, 156.5, 156.4, 156.4, 156.1, 150.6, 150.5, 150.4, 148.9, 148.8, 148.7, 145.7, 145.7, 145.6, 145.6, 144.1, 144.1, 144.0, 144.0, 131.9, 131.5, 131.4, 131.4, 131.3, 110.7, 110.5, 107.0, 104.9, 104.7, 104.7, 104.5, 49.1, 40.3, 30.0.

Example 84: (5)-6-(2,6-difluorophenyl)-2,5,6,7-tetra ydro-3H-pyrrolo[l,2-c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 59 from (E)-l,3-difluoro-2-(2- nitrovinyl)benzene using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0) and isolated as a greenish powder.

Ή NMR (DMSO-iM): 11.84 (1 Η, br s), 7.41 (1 Η, m), 7.13 (2 Η, m), 6.63 (1 Η, m), 4.47 (1 Η, quin, J = 8.7 Hz), 4.17 (1 H, dd, J = 10.8, 9.8 Hz), 3.73 (1 H, dd, J = 11.4, 8.2 Hz), 3.29 (1 H, dd, J = 15.8, 9.3 Hz), 2.92 (1 H, dd, J = 15.8, 8.4 Hz).

¹³ C NMR (DMSC M): 161.6, 161.6, 160.0, 159.9, 155.9, 132.3, 129.8, 129.7, 129.7, 116.7, 116.6, 116.4, 112.3, 112.2, 112.1, 112.1, 106.6, 48.6, 35.3, 29.6.

Example 85: (5)-6-(3-chloro-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-py rrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 59 from (E)- l-chloro-2,4-difluoro- 3-(2-nitrovinyl)benzene using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0) and isolated as a white powder.

Ή NMR (DMSO- 6): 11.85 (1 H, br s), 7.61 (1 H, td, J = 8.7, 5.6 Hz), 7.22 (1 H, dt, J = 1.6, 9.6 Hz), 6.63 (1 H, s), 4.50 (1 H, quin, J = 8.5 Hz), 4.18 (1 H, dd, J = 11.5, 9.3 Hz), 3.75 (1 H, dd, J = 11.7, 7.7 Hz), 3.31 (1 H, dd, J = 9.4, 16 Hz), 2.93 (1 H, dd, J = 15.8, 7.8 Hz).

1 ³ C NMR (DMSC M): 160.2, 160.1, 158.5, 158.5, 156.6, 156.5, 155.8, 155, 154.9, 132.3, 129.7, 129.7, 118.9, 118.8, 118.7, 116.1, 116.1, 116, 113.3, 113.3, 113.1, 113.1, 106.6, 48.5, 35.7, 29.5. Example 86: ( ?)-6-(3-chloro-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyr rolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 58 from (E)- l-chloro-2,4-difluoro- 3-(2-nitrovinyl)benzene using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7) and isolated as a white powder.

Ή NMR (DMSO- 6): 11.85 (1 Η, br s), 7.61 (1 Η, td, J = 8.7, 5.6 Hz), 7.22 (1 H, dt, J = 1.6, 9.6 Hz), 6.63 (1 H, s), 4.50 (1 H, quin, J = 8.5 Hz), 4.18 (1 H, dd, J = 11.5, 9.3 Hz), 3.75 (1 H, dd, J = 11.7, 7.7 Hz), 3.31 (1 H, dd, J = 9.4, 16 Hz), 2.93 (1 H, dd, J = 15.8, 7.8 Hz).

1 ³ C NMR (DMSC M): 160.2, 160.1, 158.5, 158.5, 156.6, 156.5, 155.8, 155, 154.9, 132.2, 129.7, 129.6, 118.9, 118.8, 118.7, 116.1, 116.1, 116, 115.9, 113.3, 113.2, 113.1, 113.1, 106.6, 48.5, 35.7, 29.5.

Example 87: ( ?)-6-(2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 58 from (E)-l,3-difluoro-2-(2- nitrovinyl)benzene using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7) and isolated as a white powder.

Ή NMR (DMSO-iM): 11.84 (1 H, br s), 7.41 (1 H, m), 7.13 (2 H, t, J = 8.1 Hz), 6.63 (1 H, s), 4.47 (1 H, quin, J = 8.7 Hz), 4.17 (1 H, m), 3.73 (1 H, dd, J = 11.4, 8.2 Hz), 3.29 (1 H, dd, J = 15.7, 9.2 Hz), 2.92 (1 H, br dd, J = 15.7, 8.4 Hz).

¹³ C NMR (DMSC M): 161.6, 161.6, 160.0, 159.9, 155.8, 132.3, 129.8, 129.8, 129.7, 116.7, 116.6, 116.4, 112.3, 112.2, 112.1, 112.1, 106.6, 48.6, 35.3, 29.6. Example 88: (5a5,6a ?)-5a-(3-chloro-2,6-difluorophenyl)-5,5<3,6,6i3- tetrahydrocyclopropa[3,4]pyrrolo[2 1 -c] [l,2,4]triazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 60 from tert-butyl (((15,2 ?)-l-(3- chloro-2,6-difluorophenyl)-2-(hydroxymethyl)cyclopropyl)meth yl)carbamate and isolated as a pink solid.

Ή NMR (DMSO-iM): 13.30 (1 Η, s), 7.67 (1 Η, td, J = 8.7, 5.6 Hz), 7.24 (1 H, td, J = 9.1, 1.4 Hz), 4.12 (1 H, d, J = 12.6 Hz), 3.86 (1 H, d, J = 12.2 Hz), 2.95 (1 H, dd, J = 8.9, 4.2 Hz), 1.81 (1 H, dd, J = 8.8, 5.9 Hz), 1.68 (1 H, m).

¹³ C NMR (DMSC M): 163.6, 161.2, 161.1, 159.5, 159.5, 157.8, 157.7, 157.5, 156.1, 156.0, 130.8, 130.7, 116.1, 116.0, 115.9, 115.8, 115.8, 115.7, 115.7, 113.0, 113.0, 112.9, 112.8, 49.5, 27.3, 20.1, 19.6.

Example 89: (5a5 ^, ,6a ?)-5a-(2-chloro-6-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

Compound was prepared in an analogous manner to Example 53 from 2-(2-chloro-6- fluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a beige solid.

Ή NMR (DMSO-iM): 11.78 (1 H, br s), 7.42 (1 H, m), 7.38 (1 H, m), 7.27 (1 H, ddd, J = 9.7, 8.3, 1.2 Hz), 6.72 (1 H, d, J = 2.2 Hz), 4.04 (1 H, br d, J = 12.0 Hz), 3.67 (1 H, d, J = 12.0 Hz), 2.73 (1 H, m), 1.67 (1 H, br s), 1.34 (1 H, t, J = 5.1 Hz).

¹³ C NMR (DMSO-iM): 162.7, 161.1, 156.5, 136.4, 134.7, 130.7, 130.6, 125.7, 125.7, 124.8, 124.7, 115.1, 114.9, 106.4, 51, 29.9, 22.8, 22.7, 22.7. Example 90: (5a5,6a ?)-5a-(3-chloro-2,6-difluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrolo[ -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(3-chloro-2,6- difluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as an orange solid. Ή NMR (DMSO-iM): 11.80 (1 Η, br s), 7.64 (1 Η, m), 7.22 (1 Η, t, J = 8.8 Hz), 6.72 (1 H, d, J = 2.1 Hz), 4.06 (1 H, d, J = 12.2 Hz), 3.76 (1 H, d, J = 12.2 Hz), 2.77 (1 H, dd, J = 8.3, 4.3 Hz), 1.69 (1 H, dd, J = 8.1, 5.6 Hz), 1.31 (1 H, t, J = 5.0 Hz).

¹³ C NMR (DMSC M): 161.3, 161.2, 159.6, 159.6, 157.8, 157.8, 156.6, 156.2, 156.1, 134.3, 130.3, 130.3, 117.1, 117.0, 116.8, 115.8, 115.7, 115.6, 115.6, 112.9, 112.9, 112.8, 112.8, 106.5, 51.4, 26.7, 21.6, 21.5. Example 91; (5aS,6a ?)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thione-5,5- d2

Compound was prepared from 2-(5-chloro-2-fluorophenyl)acetonitrile and (R)-2- (chloromethyl)oxirane using NaBD ₄ as reducing agent (Example 53 step 1) and isolated as an off-white solid.

Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.49 (1 Η, dd, J = 6.5, 2.6 Hz), 7.43 (1 H, ddd, J = 8.6, 4.3, 2.8 Hz), 7.30 (1 H, t, J = 9.4 Hz), 6.68 (1 H, s), 2.88 (1 H, dd, J = 8.3, 4.2 Hz), 1.67 (1 H, dd, J = 8.3, 5.4 Hz), 1.17 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 161.3, 159.7, 156.6, 134.6, 130.1, 130.1, 129.3, 129.3, 128.8, 128.7, 128.3, 128.3, 117.5, 117.4, 106.1, 50.9, 32.4, 22.1, 20.8.

Example 92; (5aS,6a ?)-5a-(3-chloro-2-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[ -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(3-chloro-2- fluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a beige solid.

Ή NMR (DMSO-iM): 11.77 (1 Η, br s), 7.54 (1 Η, m), 7.39 (1 Η, m), 7.21 (1 Η, t, J = 7.8 Hz), 6.69 (1 H, d, J = 2.2 Hz), 4.11 (1 H, d, J = 12.0 Hz), 3.83 (1 H, d, J = 12.2 Hz), 2.86 (1 H, dd, J = 8.4, 4.3 Hz), 1.65 (1 H, dd, J = 8.4, 5.3 Hz), 1.20 (1 H, t, J = 4.8 Hz) .

¹³ C NMR (DMSC M): 157.8, 156.7, 156.2, 134.5, 129.9, 129.4, 129.4, 128.6, 128.5, 125.4, 125.4, 119.9, 119.8, 106.2, 51.6, 51.5, 32.8, 22.1, 20.9. Example 93: (5aS,6a ?)-5a-(5-bromo-2-fluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(5-bromo-2- fluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a beige solid.

Ή NMR (DMSO-df5): 11.76 (1 H, br s), 7.61 (1 H, dd, J = 6.7, 2.5 Hz), 7.55 (1 H, ddd, J = 8.7, 4.5, 2.6 Hz), 7.24 (1 H, dd, J = 10.1, 8.8 Hz), 6.68 (1 H, d, J = 2.2 Hz), 4.09 (1 H, d, J = 12.0 Hz), 3.80 (1 H, d, J = 12.0 Hz), 2.88 (1 H, dd, J = 8.4, 4.3 Hz), 1.67 (1 H, dd, J = 8.4, 5.4 Hz), 1.16 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-df5): 161.8, 160.2, 156.6, 134.6, 133.0, 133.0, 132.4, 132.3, 129.2, 129.1, 118.0, 117.8, 116.2, 116.2, 106.2, 51.5, 51.5, 32.6, 22.1, 20.9.

Example 94: (5a5,6a ?)-5a-(3-bromo-5-fluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(3-bromo-5- fluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a dark yellow solid. Ή NMR (DMSO-df5): 11.74 (1 Η, br s), 7.43 (1 Η, s), 7.43 (1 Η, m), 7.29 (1 Η, dt, J = 10.0, 1.9 Hz), 6.66 (1 H, d, J = 2.2 Hz), 4.23 (1 H, d, J = 12.0 Hz), 4.02 (1 H, d, J = 12.2 Hz), 3.01 (1 H, dd, J = 8.4, 4.3 Hz), 1.67 (1 H, dd, J = 8.3, 5.4 Hz), 1.16 (1 H, t, J = 4.8 Hz) . ¹³ C NMR (DMSO-iM): 163.0, 161.4, 156.8, 145.0, 145.0, 134.6, 126.0, 125.9, 122.2, 122.1, 117.1, 117.0, 113.4, 113.3, 105.9, 50.8, 36.3, 36.3, 25.1, 22.8.

Example 95: (5)-6-(3,5-difluorophenyl)-l-methyl-2,5,6,7-tetrahydro-3H-py rrolo[l,2- c]imidazole-3-thione

Step 1: ((4S)-tert-butyl 2-(cyano(hydroxy)methyl)-4-(3,5-difluorophenyl)pyrrolidine-l - carboxylate

To a stirred solution of (4S)-ie/t-butyl 4-(3,5-difluorophenyl)-2-formylpyrrolidine-l -carboxylate (1.2 g, 3.85 mmol) in a mixture of tetrahydrofuran (10 mL) and water (5 mL) was added potassium cyanide (0.301 g, 4.63 mmol) followed by addition of cc HCl (0.319 mL, 3.85 mmol).

The mixture was stirred for 8 h, then extracted with dichloromethane. The organic phase was washed with brine, dried over MgSC and evaporated to dryness to give (4S)-ie/t-butyl 2-

(cyano(hydroxy)methyl)-4-(3,5-difluorophenyl)pyrrolidine- l-carboxylate as a yellowish oil. (Yield: 1.44 g, 99%).

Step 2: (4S)-tert-butyl 4-(3,5-difluorophenyl)-2-(2-ethoxy-l-hydroxy-2-oxoethyl)pyrr olidine-l- carboxylate

A mixture of (4S)-ie/t-butyl 2-(cyano(hydroxy)methyl)-4-(3,5-difluorophenyl)pyrrolidine-l - carboxylate (1.43 g, 3.80 mmol) and 2 M HCl (28.5 mL, 57.1 mmol) was stirred under reflux for

16 h. After cooling to room temperature the mixture was filtered through a celite plug to remove insoluble coloured precipitate and then the filtrate was evaporated to dryness under vacuum. The residue was azeotroped twice with dry ethanol and the residue was taken up in abs. ethanol (20 mL). The thus obtained solution was treated with 4 M HCl (9.51 mL, 38.0 mmol) in dioxane and stirred under reflux for 2 h. The mixture was evaporated to dryness, and then azeotroped with abs. ethanol. The resulting semisolid was taken up in abs. ethanol (30 niL), neutralized by addition of triethylamine to pH = 6-7, then a second crop of triethylamine (0.530 mL, 3.80 mmol) was added followed by addition of di-ie/t-butyl dicarbonate (0.830 g, 3.80 mmol). The reaction was allowed to stir at room temperature for 2 h, and then evaporated to dryness at 40 °C. The residue was partitioned between dichloro methane and water, the organic phase was dried over MgS0 ₄ and concentrated under reduced pressure. Chromatography (petroleum ether - ethyl acetate; 9:1, then 4: 1) gave the product as a yellow oil. (Yield: 1.16 g, 79%).

Step 3: (4S)-tert-buty -(3,5-difluorophenyl)-2-(2-ethoxy-2-oxoacetyl)pyrrolidine-l- carboxylate

To a stirred solution of (4S)-ie/t-butyl 4-(3,5-difluorophenyl)-2-(2-ethoxy-l-hydroxy-2- oxoethyl)pyrrolidine-l-carboxylate (1.15 g, 2.98 mmol) in dry dichloromethane (25 mL) was added Dess-Martin periodinane (3-oxo-l ⁵ -benzo[d][l,2]iodaoxole-l,l,l(3H)-triyl triacetate) (1.266 g, 2.98 mmol) at room temperature in one portion and the mixture was stirred for 2 h. The reaction mixture was concentrated under vacuum, whereupon the reside was purified by chromatography (petroleum ether - ethyl acetate; 4: 1). The product was isolated as a yellowish oil. (1.08 g, 94% yield).

Step 4: ethyl 2-((4S)-4-(3, -dtfluorophenyl)pyrrolidin-2-yl)-2-oxoacetate hydrochloride

To a stirred solution of (4S)-ie/t-butyl 4-(3,5-difluorophenyl)-2-(2-ethoxy-2- oxoacetyl)pyrrolidine-l-carboxylate (0.4 g, 1.043 mmol) in 4 M HC1 (5.22 mL, 20.87 mmol) in dioxane was stirred at room temperature for 4 h. The reaction mixture was diluted with a mixture of diethyl ether (20 mL) and petroleum ether (5 mL) and stirred for 30 min, Thereupon, the resulting precipitate was collected, washed with diethyl ether, petroleum ether and dried under vacuum at 50 °C to give ethyl 2-((4S)-4-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-oxoacetate hydrochloride as a white powder. (Yield: 0.34 g, 92%).

Step 5: (S)-ethyl 6-(3,5-difluorophenyl)-3-thioxo-3,5,6, 7 -tetrahydro-2H-pyrrolo[ 1 ,2-c]imidazole- -carboxylate

A solution of ethyl 2-((45)-4-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-oxoacetate hydrochloride (0.33 g, 1.032 mmol), 6 M HCl (0.086 mL, 0.516 mmol) and potassium thiocyanate (0.110 g, 1.135 mmol) in a mixture of ethanol (5 mL) and water (5 mL) was stirred under reflux for 30 min.. The reaction was then cooled to room temperature, and the resulting solid was collected, washed with a mixture of ethanol and water (1: 1), and dried under vacuum at 50 °C to give (S)- ethyl 6-(3,5-difluorophenyl)-3-thioxo-3,5,6,7-tetrahydro-2H-pyrrol o[l,2-c]imidazole-l- carboxylate as a white solid. (Yield: 0.28 g, 84%).

Step 6: 5)-6-(3,5-difluorophenyl)-l-methyl-6,7-dihydro-2H-pyrrolo[l, 2-c]imidazole-3(5H)- thione

To a solution of (S)-ethyl 6-(3,5-difluorophenyl)-3-thioxo-3,5,6,7-tetrahydro-2H-pyrrol o[l,2- c] imidazole- 1 -carboxylate (0.1 g, 0.308 mmol) in dry tetrahydrofuran (2 mL) was added sodium borohydride (0.058 g, 1.542 mmol) followed by addition of boron trifluoride etherate (0.195 mL, 1.542 mmol) with ice-water bath cooling. The mixture was allowed to warm up to room temperature and stirred for 16 h. Thereupon, the mixture was cooled again to 0-5 °C, and quenched with 2 M HCl (1.233 ml, 2.467 mmol). The organic solvents were removed under vacuum, and then the residue extracted with ethyl acetate. The organic phase was dried over MgS0 ₄ , filtered and evaporated to dryness. Chromatography (petroleum ether - ethyl acetate; 1 : 1 gave (5)-6-(3,5-difluorophenyl)- l-methyl-6,7-di ydro-2H-pyrrolo[l,2-c]imidazole-3(5H)- thione as a white powder (0.021 g, 0.079 mmol, 25.6% yield).

Ή NMR (DMSO-iM): 11.69 (1 Η, br s), 7.13 (3 Η, m), 5.76 (1 Η, s), 4.15 (1 Η, dd, J = 11.2, 7.9 Hz), 4.07 (1 H, quin, J = 7.8 Hz), 3.66 (1 H, dd, J = 11.2, 8.4 Hz), 3.18 (1 H, m), 2.82 (1 H, ddd, J = 15.0, 8.9, 1.3 Hz), 1.98 (3 H, s).

¹³ C NMR (DMSO-iM): 163.3, 163.2, 161.7, 161.6, 155.1, 145.7, 145.7, 145.6, 127.8, 115.4, 110.8, 110.7, 110.6, 110.6, 102.6, 102.5, 102.3, 50.0, 46.5, 30.0, 9.4.

Example 96: ( ?)- l-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahydro-3H -pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 80 from {AR)- \-{tert- butoxycarbonyl)-4-(2,3,5,6-tetrafluorophenyl)pyrrolidine-2-c arboxylic acid and methylmagnesium iodide and isolated as an off-white powder.

Ή NMR (DMSO-iM): 11.74 (1 Η, br s), 7.85 (1 Η, m), 4.49 (1 Η, quin, J = 8.5 Hz), 4.42 (1 H, m), 4.15 (1 H, dd, J = 11.6, 9.2 Hz), 3.76 (1 H, dd, J = 11.7, 7.8 Hz), 3.27 (1 H, dd, J = 15.6, 9.2 Hz), 2.89 (1 H, dd, J = 15.4, 7.9 Hz), 1.97 (3 H, s) .

¹³ C NMR (DMSO-iM): 155.0, 146.4, 146.3, 146.3, 145.3, 145.2, 144.8, 144.7, 144.6, 143.7, 143.6, 127.5, 120.5, 120.4, 120.3, 115.3, 105.9, 105.7, 105.6, 48.4, 35.9, 28.6, 9.3.

Example 97: (5)- l-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahydro-3H -pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 80 from { S)- \-{tert- butoxycarbonyl)-4-(2,3,5,6-tetrafluorophenyl)pyrrolidine-2-c arboxylic acid and methylmagnesium iodide and isolated as a light beige powder.

Ή NMR (DMSO-iM): 11.74 (1 H, br s), 7.85 (1 H, m), 4.49 (1 H, quin, J = 8.5 Hz), 4.15 (1 H, dd, J = 11.6, 9.2 Hz), 3.76 (1 H, dd, J = 11.7, 7.8 Hz), 3.27 (1 H, dd, J = 15.6, 9.2 Hz), 2.89 (1 H, dd, J = 15.4, 7.9 Hz), 1.97 (3 H, s).

¹³ C NMR (DMSO-iM): 155, 146.4, 146.3, 146.3, 145.3, 145.2, 144.8, 144.7, 144.6, 143.7, 143.6, 127.5, 120.5, 120.4, 120.3, 115.3, 105.9, 105.7, 105.6, 48.7, 48.4, 35.9, 28.6, 9.3.

Example 98: (5)-6-(2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 80 from {AS)- \-{tert- butoxycarbonyl)-4-(2,6-difluorophenyl)pyrrolidine-2-carboxyl ic acid and methylmagnesium iodide and isolated as a light beige powder.

Ή NMR (DMSO-iM): 11.72 (1 Η, br s), 7.40 (1 Η, m), 7.13 (2 Η, m), 4.41 (1 Η, quin, J = 8.7 Hz), 4.12 (1 H, br t, J = 10.1 Hz), 3.70 (1 H, dd, J = 8.8, 10.8 Hz), 3.21 (1 H, br dd, J = 15.3, 9.2 Hz), 2.84 (1 H, br dd, J = 15.2, 8.6 Hz), 1.97 (3 H, s) .

1 ³ C NMR (DMSC M): 161.6, 161.6, 160.0, 159.9, 155.0, 129.8, 129.7, 129.7, 127.8, 116.6, 116.5, 116.4, 115.2, 112.3, 112.2, 112.1, 112.1, 48.6, 35.4, 28.8, 9.3. Example 99: (5aS,6a ?)-5a-(5-chloro-2-fluorophenyl)-l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 80 from tert-butyl (15,5 ?)-l-(5- chloro-2-fluorophenyl)-4-(methoxy(methyl)carbamoyl)-3-azabic yclo[3.1.0]hexane-3- carboxylate and methylmagnesium iodide. The product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.65 (1 Η, br s), 7.47 (1 Η, dd, J = 6.5, 2.6 Hz), 7.42 (1 H, ddd, J = 8.8, 4.4, 2.7 Hz), 7.29 (1 H, dd, J = 10.0, 8.9 Hz), 4.06 (1 H, d, J = 11.7 Hz), 3.77 (1 H, d, J = 12.0 Hz), 2.87 (1 H, dd, J = 8.2, 4.3 Hz), 2.04 (3 H, m), 1.64 (1 H, dd, J = 8.1, 5.4 Hz), 1.12 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 161.3, 159.7, 155.7, 130.3, 130.1, 130.1, 129.3, 129.3, 129.0, 128.9, 128.3, 128.3, 117.6, 117.4, 114.8, 51.5, 51.5, 32.3, 22.3, 20.2, 9.4. Example 100: (5a5,6a/?)-5a-(5-chloro-2-fluorophenyl)-l-(methyl-<i3)-5, 5a,6,6a- tetrahydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 80 from tert-butyl (15,5 ?)-l-(5- chloro-2-fluorophenyl)-4-(methoxy(methyl)carbamoyl)-3-azabic yclo[3.1.0]hexane-3- carboxylate and methyl-<¾-magnesium iodide. The product was isolated as a light orange solid. Ή NMR (DMSO-ίΜ): 11.65 (1 H, s), 7.47 (1 H, dd, J = 6.6, 2.8 Hz), 7.42 (1 H, ddd, J = 8.8, 4.4, 2.7 Hz), 7.29 (1 H, m), 4.06 (1 H, d, J = 11.9 Hz), 3.77 (1 H, d, J = 12.0 Hz), 2.87 (1 H, dd, J = 8.3, 4.3 Hz), 1.64 (1 H, dd, J = 8.3, 5.4 Hz), 1.12 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSC M): 161.3, 159.7, 155.7, 155.6, 130.3, 130.1, 130.1, 129.3, 129.3, 129.0, 128.9, 128.3, 128.3, 117.6, 117.4, 114.7, 114.6, 51.5, 51.5, 32.3, 22.3, 20.2.

Example 101: (5a5,6a/?)-5a-(5-chloro-2-fluorophenyl)-2-(methyl-<i3)-5, 5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3 2H)-thione

Compound was prepared in an analogous manner to Example 76 from (17?,5S)-5-(5-chloro-2- fluorophenyl)-3-azabicyclo[3.1.0]hexane-2-carbaldehyde hydrochloride and isothiocyanatomethane-<¾ and isolated as a yellow oil.

Ή NMR (DMSO-iM): 7.50 (1 Η, dd, J = 6.5, 2.5 Hz), 7.43 (1 H, m), 7.30 (1 H, t, J = 9.5 Hz), 6.93 (1 H, s), 4.13 (1 H, br d, J = 12.0 Hz), 3.84 (1 H, d, J = 12.0 Hz), 2.92 (1 H, dd, J = 8.2, 4.1 Hz), 1.69 (1 H, dd, J = 8.3, 5.5 Hz), 1.17 (1 H, t, J = 4.8 Hz).

¹³ C NMR (DMSO-iM): 161.3, 159.7, 157.2, 132.9, 130.2, 130.2, 129.4, 129.4, 128.7, 128.6, 128.3, 128.3, 117.6, 117.4, 110.4, 52.3, 52.3, 32, 22.1, 20.9.

Example 102: 5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a-tetrahydrocyclopropa[ 3,4]pyrrolo[l,2- c]imidazole-3(2H)-thione-6,6,6 -<¾

Compound was prepared in an analogous manner to Example 53 from 2-(5-chloro-2- fluorophenyl)acetonitrile and 2-(chloromethyl-d2)oxirane-2,3,3-<i.? and isolated as a beige solid. Ή NMR (DMSO-iM): 11.76 (1 H, br s), 7.49 (1 H, dd, J = 6.5, 2.7 Hz), 7.43 (1 H, ddd, J = 8.8, 4.4, 2.8 Hz), 7.30 (1 H, dd, J = 10.0, 8.8 Hz), 6.68 (1 H, d, J = 2.3 Hz), 4.10 (1 H, dd, J = 12.0, 1.8 Hz), 3.81 (1 H, d, J = 12.0 Hz).

¹³ C NMR (DMSC M): 161.3, 159.7, 156.6, 134.5, 130.2, 130.2, 129.4, 129.3, 128.8, 128.7, 128.3, 128.3, 117.6, 117.4, 106.2, 51.5, 51.4, 32.4, 21.6, 21.4, 21.2, 20.6, 20.5, 20.3.

Example 103: (5a ?,6aS)-5a-(3-chloro-2,6-difluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrolo[ -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(3-chloro-2,6- difluorophenyl)acetonitrile and (S)-2-(chloromethyl)oxirane and isolated as a beige solid.

Ή NMR (DMSO-iM): 11.79 (1 Η, br s), 7.64 (1 Η, m), 7.21 (1 Η, t, J = 8.7 Hz), 6.71 (1 H, d, J = 2.2 Hz), 4.05 (1 H, d, J = 12.2 Hz), 3.76 (1 H, d, J = 12.3 Hz), 2.76 (1 H, dd, J = 8.4, 4.4 Hz), 1.69 (1 H, dd, J = 8.2, 5.6 Hz), 1.30 (1 H, t, J = 5.0 Hz) .

¹³ C NMR (DMSC M): 161.3, 161.2, 159.6, 159.6, 157.8, 157.8, 156.6, 156.2, 156.1, 134.3, 130.3, 130.3, 117.1, 117.0, 116.8, 115.8, 115.7, 115.7, 115.6, 113.0, 112.9, 112.8, 112.8, 106.5, 51.4, 26.7, 21.6, 21.5.

Example 104: ( ?)-6-(3-chloro-2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 80 from {AS)- \-{tert- butoxycarbonyl)-4-(3-chloro-2,6-difluorophenyl)pyrrolidine-2 -carboxylic acid and methylmagnesium iodide and isolated as an off-white powder.

Ή NMR (DMSO-iM): 11.73 (1 H, br s), 7.61 (1 H, td, J = 8.8, 5.6 Hz), 7.21 (1 H, t, J = 9.5 Hz), 4.44 (1 H, quin, J = 8.6 Hz), 4.13 (1 H, dd, J = 11.4, 9.2 Hz), 3.72 (1 H, dd, J = 11.6, 7.9 Hz), 3.23 (1 H, m), 2.84 (1 H, dd, J = 15.5, 8.1 Hz), 1.97 (3 H, s).

¹³ C NMR (DMSC M): 160.2, 160.1, 158.5, 158.5, 156.6, 156.5, 155, 154.9, 154.9, 129.7, 129.7, 127.7, 118.9, 118.7, 118.6, 116.1, 116.1, 116.0, 116.0, 115.2, 113.3, 113.3, 113.1, 113.1, 48.5, 35.8, 28.7, 9.4.

Example 105: (5)-6-(3-chloro-2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 80 from {AR)- \-{tert- butoxycarbonyl)-4-(3-chloro-2,6-difluorophenyl)pyrrolidine-2 -carboxylic acid and methylmagnesium iodide and isolated as a light beige powder.

Ή NMR (DMSO-iM): 11.73 (1 Η, br s), 7.61 (1 Η, td, J = 8.8, 5.6 Hz), 7.21 (1 H, t, J = 9.5 Hz), 4.44 (1 H, quin, J = 8.6 Hz), 4.13 (1 H, dd, J = 11.4, 9.2 Hz), 3.72 (1 H, dd, J = 11.6, 7.9 Hz), 3.23 (1 H, m), 2.84 (1 H, dd, J = 15.5, 8.1 Hz), 1.97 (3 H, s). ¹³ C NMR (DMSC M): 160.2, 160.1, 158.5, 158.5, 156.6, 156.5, 154.9, 154.9, 129.7, 129.6, 127.7, 118.9, 118.7, 118.6, 116.1, 116.1, 116.0, 115.9, 115.2, 113.3, 113.3, 113.1, 113.1, 48.5, 35.7, 28.7, 9.4. Example 106: (5aS,6aS)-5a-(3,5-difluorophenyl)-2,5,5a,6,6a,7-hexahydro-3H - cyclopropa[d]imidazo[l,5-a]pyridine-3-thione

Step 1: (( lR,2S)-2-( ( ( tert-butoxycarbonyl)amino )methyl)-2-( 3,5- difluorophenyl)cyclopropyl)methyl 4-methylbenzenesulfonate

To a stirred solution of tert-batyl (( \S,2R)- 1-(3, 5-difluorophenyl)-2- (hydroxymethyl)cyclopropyl)methylcarbamate ( 1.0 g, 3.19 mmol) (prepared according to Example 53 from 2-(3,5-difluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane)) in dry dichloromethane (10 mL) was added triethylamine (0.89 mL, 6.38 mmol) followed by addition of N,N-dimethylpyridin-4-amine (0.039 g, 0.319 mmol) and tosyl chloride (0.730 g, 3.83 mmol) at 0-5 °C under nitrogen. The mixture was stirred for 2 h in ice and then allowed to warm up naturally to room temperature over 30 min. Thereupon, the mixture was washed with sodium bicarbonate solution, 10% citric acid, then dried over MgSC and finally evaporated to give the crude product as a light brown oil (1.37 g, 73% yield).

Step 2: tert-butyl (((lS,2S)-2-(cyanomethyl)-l-(3,5- difluorophenyl)cyclopropyl)methyl)carbamate

To a solution of sodium cyanide (0.204 g, 4.16 mmol) in dimethyl solfoxide (12 mL) was added ((1 ?,25)-2-((ieri-butoxycarbonylamino)methyl)-2-(3,5-difluoroph enyl)cyclopropyl)methyl 4- methylbenzenesulfonate (1.35 g, 2.310 mmol) and the mixture was stirred at room temperature for 4 h. The reaction was then diluted with water (30 mL) followed by extraction with diethyl ether. The organic phase was washed with brine, dried over MgSC and evaporated to dryness. The resulting oil was crystallised from petroleum ether, filtered and dried under vacuum to give tert-butyl ((15,25)-2-(cyanomethyl)-l-(3,5-difluorophenyl)cyclopropyl)m ethylcarbamate as a light beige powder (0.57 g, 77% yield).

Step 3: tert-butyl (((lS,2S)-2-(2-amino-2-oxoethyl)-l-(3,5- difluorophenyl)cyclopropyl)methyl)carbamate

To a solution of tert- butyl (( 15,25)-2-(cyano methyl)- 1 -(3,5- difluorophenyl)cyclopropyl)methylcarbamate (1.69 g, 5.24 mmol) in a mixture of acetone (30 mL) and water (10 mL) was added urea hydrogen peroxide addition complex (2.466 g, 26.2 mmol) followed by addition of potassium carbonate (0.145 g, 1.049 mmol) and the mixture was stirred at room temperature for 20 h. Acetone was then removed under vacuum and the residue was partitioned between water and a mixture of ethyl acetate and petroleum ether (1: 1). The organic phase was dried over MgSC and evaporated to dryness to give the title product as a colourless oil (1.98 g, 100% yield).

Step 4: (lS,6S)-l-(3, 5-difluorophenyl)-3-azabicyclo[4.1.0 ]heptan-4-one

ie/t-Butyl ((15,25)-2-(2-amino-2-oxoethyl)-l-(3,5-difluorophenyl)cyclop ropyl)methylcarbamate (1.78 g, 5.23 mmol) was stirred under reflux with 2 M HC1 (39 mL, 78 mmol) for 2 h. Thereupon, the mixture was evaporated to dryness and then azeotroped with abs. ethanol. The oily residue was dissolved in abs. ethanol (80 mL) followed by addition of 4 M HC1 (13.0 mL, 52.1 mmol) in dioxane. The thus obtained solution was stirred under reflux for 30 min and evaporated to dryness. The residue was taken up in methanol (20 mL), and then pH was adjusted to 9-10 by addition of 25% sodium methoxide in methanol. The mixture was stirred overnight at

50-55 °C. Methanol was then removed under vacuum, and the residue crystallized form water.

The resulting solid was collected, washed with water and dried to give (15,65)-l-(3,5- difluorophenyl)-3-azabicyclo[4.1.0]heptan-4-one as a beige powder (0.9 g, 77% yield).

Step 5: tert-butyl (lS,6S)-l-(3,5-difluorophenyl)-4-oxo-3-az bicyclo[4.1.0]heptane-3- carboxylat

To a solution of (15,65)-l-(3,5-difluorophenyl)-3-azabicyclo[4.1.0]heptan-4-o ne (0.88 g, 3.94 mmol) and N,N-dimethylpyridin-4-amine (0.482 g, 3.94 mmol) in dry dichloro methane (3 mL) was added di-ie/t-butyl dicarbonate (1.291 g, 5.91 mmol) at room temperature in portions. The mixture was stirred for 4 h at room temperature, then diluted with dichloromethane to 50 mL and finally washed with 10% citric acid (25 mL). The organic phase was dried over MgSC , filtered on a silica pad, and then the filtrate evaporated to dryness to give {\SfiS)-tert-buty\ l-(3,5- difluorophenyl)-4-oxo-3-azabicyclo[4.1.0]heptane-3-carboxyla te as a light beige powder (1.18 g, 93% yield).

Step 6: tert-butyl (lS,6S)-l-(3,5-difluorophenyl)-4-hydroxy-3-azabicyclo[4.1.0] heptane-3- carboxylate

To a solution of {\SfiS)-tert-buty\ l-(3,5-difluorophenyl)-4-oxo-3-azabicyclo[4.1.0]heptane-3- carboxylate (1.17 g, 3.62 mmol) in a mixture of dry diethyl ether (18 mL) and tetrahydrofuran (6 mL) was added dropwise 65% RED-A1 (bis(2-methoxyethoxy)aluminum(III) sodium hydride) (2.17 mL, 7.24 mmol) in toluene at 0-5 °C and the mixture was stirred for 30 min. under nitrogen. The mixture was then quenched with a cold solution of saturated sodium bicarbonate and allowed to stir at ambient for 30 min. The organic phase was separated, and the aqueous phase was extracted with diethyl ether. The combined organic phases were dried over MgSC and evaporated to dryness to give (lS,6S)-tert-butyl l-(3,5-difluorophenyl)-4-hydroxy-3- azabicyclo[4.1.0]heptane-3-carboxylate as a yellowish oil.(1.15 g, 98% yield).

Step 7 tert-butyl (lS,6S)-l-(3,5-difluorophenyl)-4-methoxy-3-azabicyclo[4.1.0] heptane-3- carboxylate

To a solution of l-(3,5-difluorophenyl)-4-hydroxy-3-azabicyclo[4.1.0]heptane- 3-carboxylate (1.14 g, 3.50 mmol) in methanol (35 mL) was added 4-methylbenzenesulfonic acid hydrate (0.067 g, 0.350 mmol) at room temperature and the solution was stirred for 24 h. Thereupon, the mixture was neutralized with 1 M sodium hydroxide (0.35 mL, 0.350 mmol) and evaporated to dryness. The residue was taken up in a mixture of petroleum ether and ethyl acetate (4:1), then chromatographed in a mixture of petroleum ether - ethyl acetate (9: 1), to give {\SfiS)-tert-buty\ l-(3,5-difluorophenyl)-4-methoxy-3-azabicyclo[4.1.0]heptane- 3-carboxylate as a colourless oil (0.71 g, 60% yield).

Step 8 tert-butyl (lS,6S)-4-cyano-l-(3,5-difluorophenyl)-3-azabicyclo[4.1.0]he ptane-3- carboxylate

To a solution of l-(3,5-difluorophenyl)-4-methoxy-3- azabicyclo[4.1.0]heptane-3-carboxylate (0.71 g, 2.092 mmol) in dry dichloro methane (15 mL) was added trimethylsilanecarbonitrile (0.561 mL, 4.18 mmol) followed by addition of boron trifluoride etherate (0.58 mL, 4.60 mmol) at -70 °C. The mixture was stirred for 4 h in the cold, and then quenched with aqueous sodium bicarbonate and allowed to warm up to room temperature. The organic phase was dried over MgSCn and evaporated to dryness. Chromatography petroleum ether - ethyl acetate; 9: 1) afforded the product as a colourless oil (0.095 g, 13%).

Step 9 tert-butyl (lS,6S)-4-carbamoyl-l-(3,5-difluorophenyl)-3-azabicyclo[4.1. 0]heptane-3- carboxylate

To a solution of 4-cyano-l-(3,5-difluorophenyl)-3-azabicyclo[4.1.0]heptane-3- carboxylate (0.09 g, 0.269 mmol) in a mixture of acetone (1.5 mL) and water (0.5 mL) was added urea hydrogen peroxide addition complex (0.127 g, 1.346 mmol) followed by addition of potassium carbonate (0.0074 mg, 0.054 mmol) and the solution was stirred at room temperature for 16 h. Acetone was then removed under vacuum, the oily residue was diluted with water (2 mL) and then extracted with a mixture of petroleum ether-ethyl acetate (1: 1). The organic phase was dried over MgSC and evaporated to dryness to give {\SfiS)-tert-buty\ 4-carbamoyl-l-(3,5- difluorophenyl)-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.09 g, 95% yield).

Step 10 (lS,6S)-3-(tert-butoxycarbonyl)-l-(3,5-difluorophenyl)-3-aza bicyclo[4.1.0]heptane-4- carboxyl acid

A suspension of (15,65)-ieri-butyl 4-carbamoyl-l-(3,5-difluorophenyl)-3- azabicyclo[4.1.0]heptane-3-carboxylate (0.09 g, 0.255 mmol) in 2 M HCI (1.92 mL, 3.83 mmol) was stirred under reflux for 3 h. The reaction mixture was concentrated under vacuum, the residue was dissolved in water and then the pH was adjusted to 7 by adding 1 M sodium hydroxide (0.511 mL, 0.511 mmol). The solution was concentrated to 2 mL, followed by addition of methanol (2 mL) and di-ie/t-butyl dicarbonate (0.123 g, 0.562 mmol). The mixture was stirred for 45 min, whereupon a second crop of di-ie/t-butyl dicarbonate (0.347 g, 1.592 mmol) was added and the reaction was stirred for 1 h. Thereupon, methanol was removed under vacuum, the residue was diluted with water (10 mL) and washed with petroleum ether. The aqueous phase was acidified to pH = 2 by adding 2 M HC1, and then extracted with dichloromethane. The organic phase was dried over MgSC , filtered and evaporated to dryness to give the product as an off-white powder (0.07 g, 78% yield).

Step 11 tert-butyl (lS,6S)-l-(3,5-difluorophenyl)-4-(hydroxymethyl)-3-az bicyclo[4.1.0]heptane- 3-carboxylate

To a solution of (15,65)-3-(ieri-butoxycarbonyl)-l-(3,5-difluorophenyl)-3- azabicyclo[4.1.0]heptane-4-carboxylic acid (0.07 g, 0.198 mmol) in isopropyl acetate (1.5 mL) was added sodium borohydride (0.018 g, 0.475 mmol) at 0-5 °C followed by addition of boron trifluoride etherate (0.075 mL, 0.594 mmol). The mixture was stirred in the cold for 2 h, then a second crop of sodium borohydride (0.018 g, 0.475 mmol) and boron trifluoride etherate (0.075 mL, 0.594 mmol) was added. After being stirred for 30 min. in the cold the reaction mixture was quenched with 1 M sodium hydroxide (1.070 mL, 1.070 mmol) and stirred at room temperature for 30 min. The organic phase was separated, dried over MgSC and evaporated to dryness to give {\SfiS)-tert-buty\ l-(3,5-difluorophenyl)-4-(hydroxymethyl)-3-azabicyclo[4.1.0] heptane-3- carboxylate as a white powder (0.066 g, 98% yield).

Step 12 tert-butyl (lS,6S)-l-(3,5-difluorophenyl)-4-formyl-3-azabicyclo[4.1.0]h eptane-3- carboxylate

To a solution of l-(3,5-difluorophenyl)-4-(hydroxymethyl)-3- azabicyclo[4.1.0]heptane-3-carboxylate (0.066 g, 0.194 mmol) in dry dichloromethane (2 mL) was added Dess-Martin periodinane (3-oxo- 1 ⁵ -benzo [d] [1,2] iodaoxole- 1,1,1 (3H)-triy 1 triacetate) (0.082 g, 0.194 mmol) in one portion to give a clear solution. The mixture was stirred for 2 h at room temperature, and then concentrated under vacuum. Chromatography (petroleum ether - ethyl acetate; 9: 1, then 4: 1) gave (15,65)-ieri-butyl l-(3,5-difluorophenyl)-4-formyl-3- azabicyclo[4.1.0]heptane-3-carboxylate as a yellowish oil (0.054 g, 82% yield).

Step 13 (5aS,6aS)-5a-(3,5-difluorophenyl)-2,5,5a,6,6a, 7-hexahydro-3H- cyclopropa[ midazo[l,5-a]pyridine-3-thione

A solution of (15,65)-ieri-butyl l-(3,5-difluorophenyl)-4-formyl-3-azabicyclo[4.1.0]heptane-3 - carboxylate (0.054 g, 0.160 mmol) in 4 M HCl (0.6 mL, 2.401 mmol) in dioxane was stirred at room temperature for 2 h. The mixture was then diluted with petroleum ether (10 mL) and stirred for 1 h. The resulting oily precipitate was dissolved in a mixture of ethanol (1 mL) and water (1 mL), and potassium thiocyanate (0.017 g, 0.176 mmol) was then added followed by addition of 6 M HCl (0.013 mL, 0.080 mmo) and the solution was stirred under reflux for 1 h. The product crystallized on cooling to room temperature. The mixture was then stirred at room temperature for 30 min, the crystals were collected and washed with a mixture of ethanol - water (1: 1) to give (5a5,6a5)-5a-(3,5-difluorophenyl)-5a,6,6a,7-tetrahydro-2H-cy clopropa[<i]imidazo[l,5- a]pyridine-3(5H)-thione as alight beige powder (0.023 g, 0.083 mmol, 52% yield).

Ή NMR (DMSO-iM): 12.06 (1 Η, br s), 7.15 (3 Η, m), 6.71 (1 Η, t, J = 1.8 Hz), 4.61 (1 H, d, J = 13.1 Hz), 3.92 (1 H, d, J = 13.1 Hz), 3.11 (1 H, ddd, J = 2.0, 3.3, 15.9 Hz), 2.99 (1 H, dd, J = 2.2, 15.9 Hz), 1.68 (1 H, m), 1.05 (1 H, dd, J = 8.9, 5.8 Hz), 0.52 (1 H, t, J = 5.7 Hz).

1 ³ C NMR (DMSO-iM): 163.4, 163.3, 161.7, 161.7, 159.4, 147.2, 147.2, 147.1, 123.9, 110.9, 110.9, 110.8, 110.7, 110.1, 102.4, 102.3, 102.1, 44.3, 23.5, 20.5, 18.6, 11.6.

Example 107: (6 ?,75)-7-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahy d] pyrrolo[l,2-c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 58 from (E)- 1,2,4, 5-tetrafluoro-2- (2-nitrovinyl)benzene and diethyl 2-methylmalonate using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst CAS # 70877-75-7). The title compound was isolated as an off-white powder.

Ή NMR (DMSO-iM): 11.87 (1 H, br s), 7.89 (1 H, m), 6.70 (1 H, t, J = 2.0 Hz), 4.20 (1 H, dd, J = ), 4.04 (1 H, q, J = 9.1 Hz), 3.84 (1 H, dd, J = 11.2, 9.4 Hz), 3.40 (1 H, m), 1.23 (3 H, d, J = 6.6 Hz).

¹³ C NMR (DMSC M): 156.0, 146.5, 146.4, 146.3, 145.6, 145.5, 144.8, 144.8, 144.7, 144.0, 143.8, 136.7, 118.4, 118.3, 118.2, 106.7, 106.2, 106.1, 105.9, 47.5, 44.6, 37.6, 17.1.

(6 ?,7 ?)-7-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahyd] 3-thion

Compound was prepared in an analogous manner to Example 58 from (E)- 1,2,4, 5-tetrafluoro-2- (2-nitrovinyl)benzene and diethyl 2-methylmalonate using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst CAS # 70877-75-7). The title compound was isolated as a light beige powder.

Ή NMR (DMSO- 6): 11.77 (1 H, br s), 7.86 (1 H, m), 6.63 (1 H, m), 4.56 (1 H, td, J = 8.5, 4.4 Hz), 4.19 (1 H, dd, J = 12.3, 8.3 Hz), 4.04 (1 H, dd, J = 12.3, 4.4 Hz), 3.74 (1 H, quin, J = 7.2 Hz), 0.87 (3 H, d, J = 7.0 Hz). ¹³ C NMR (DMSO-iM): 155.8, 146.4, 146.3, 146.2, 145.5, 145.4, 144.8, 144.7, 144.6, 143.8, 143.7, 137.2, 118.7, 118.5, 118.4, 106.2, 106.0, 105.9, 105.7, 47.7, 41.7, 34.3, 14.2.

Example 109: (5aS,6a/?)-5a-(3,5-dichlorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

Compound was prepared in an analogous manner to Example 53 from 2-(3,5- dichlorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a yellow solid.

Ή NMR (DMSO-iM): 11.74 (1 Η, br s), 7.49 (1 Η, t, J = 1.8 Hz), 7.44 (2 H, d, J = 1.8 Hz), 6.67 (1 H, s), 4.24 (1 H, d, J = 12.2 Hz), 4.02 (1 H, d, J = 12.0 Hz), 3.03 (1 H, dd, J = 8.4, 4.3 Hz), 1.68 (1 H, dd, J = 8.4, 5.3 Hz), 1.16 (1 H, t, J = 4.8 Hz) .

¹³ C NMR (DMSC M): 156.8, 144.4, 134.6, 134.2, 126.4, 105.9, 50.8, 36.3, 24.9, 22.6.

Example 110: (5a/?,6aS)-5a-(5-chloro-2-fluorophenyl)-5,5a,6,6a- tetra ydrocyclopropa[3,4]pyrrol -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 53 from 2-(5-chloro-2- fluorophenyl)acetonitrile and (S)-2-(chloromethyl)oxirane and isolated as a beige solid.

Ή NMR (DMSO-iM): 11.76 (1 Η, br s), 7.49 (1 Η, dd, J = 6.5, 2.7 Hz), 7.43 (1 H, ddd, J = 8.8, 4.4, 2.7 Hz), 7.30 (1 H, dd, J = 10.0, 8.8 Hz), 6.69 (1 H, d, J = 2.3 Hz), 4.10 (1 H, d, J = 12.0 Hz), 3.81 (1 H, d, J = 12.2 Hz), 2.89 (1 H, dd, J = 8.3, 4.2 Hz), 1.67 (1 H, dd, J = 8.4, 5.4 Hz), 1.17 (1 H, t, J = 4.7 Hz). ¹³ C NMR (DMSC M): 161.3, 159.7, 156.6, 134.6, 130.2, 130.1, 129.4, 129.3, 128.8, 128.7, 128.3, 128.3, 117.6, 117.4, 106.2, 51.5, 51.5, 32.6, 22.1, 20.9.

Example 111; (6R)-6-(2,3,5,6-tetrafluorophenyl)tetrahydro-lH-pyrrolo[l,2- c]irrddazole-3(2H)- thione

Step 1: tert-butyl (4R)-2-((l,3-dioxoisoindolin-2-yl)methyl)-4-(2, 3,5,6- tetrafluorophenyl)pyrrolidine-l-carboxylate

To a stirred solution of {AR)-tert-buty\ 2-(hydroxymethyl)-4-(2,3,5,6- tetrafluorophenyl)pyrrolidine-l-carboxylate (analogous to Example 58 step 10) (0.49 g, 1.262 mmol), phtalimide (0.312 g, 2.121 mmol) and triphenylphosphine (0.546 g, 2.083 mmol) in tetrahydrofuran (10 mL) was added dropwise under nitrogen at 0-5 °C with stirring diethyl (E)- diazene-l,2-dicarboxylate (0.32 mL, 2.02 mmol). The mixture was allowed to warm up naturally to room temperature and stirred for 64 h. The mixture was then evaporated to dryness under vacuum and the residue was purified by chromatography (petroleum ether - ethyl acetate; 9: 1, then 4: 1) to give (4R)-tert-butyl 2-((l,3-dioxoisoindolin-2-yl)methyl)-4-(2,3,5,6- tetrafluorophenyl)pyrrolidine-l-carboxylate as a foam (0.502 g, 83% yield),

Step 2: ((4R)-4-(2,3, -tetrafluorophenyl)pyrrolidin-2-yl)methanamine dihydrochloride

A mixture of (4R)-tert-butyl 2-((l,3-dioxoisoindolin-2-yl)methyl)-4-(2,3,5,6- tetrafluorophenyl)pyrrolidine-l-carboxylate (0.49 g, 1.024 mmol) and 8 M HCI (16 mL, 128 mmol) was stirred under reflux for 7 h. The solution was then cooled to room temperature and evaporated to dryness. The residue was slurried in tetrahydrofuran, the resulting solid was collected, washed with tetrahydrofuran, and petroleum ether, and dried under vacuum at 50 °C to give ((4 ?)-4-(2,3,5,6-tetrafluorophenyl)pyrrolidin-2-yl)methanamine dihydrochloride as a white powder (0.265 g, 81% yield).

Step 3: ( -6-(2,3,5,6-tetrafluorophenyl)hexahydro-3H-pyrrolo[l,2-c]imi dazole-3-thione

To a mixture of ((4 ?)-4-(2,3,5,6-tetrafluorophenyl)pyrrolidin-2-yl)methanamine dihydrochloride (0.24 g, 0.747 mmol) and triethylamine (0.229 mL, 1.644 mmol) in dry tetrahydrofuran (7.5 mL) was added in portions with stirring di(lH-imidazol-l-yl)methanethione (0.133 g, 0.747 mmol) and the mixture was stirred at room temperature for 30 min. Tetrahydrofuran was then removed under vacuum, the residue was suspended in 1 M HC1 (20 mL) with sonication. The thus obtained solid was collected, washed with water and dried under vacuum at 50 °C. The crude product was filtered through a short silica pad in a mixture of ethyl acetate - dichloromethane to give (6 ?)-6-(2,3,5,6-tetrafluorophenyl)tetrahydro-lH-pyrrolo[l,2-c] imidazole-3(2H)-thione as a white powder (0.12 g, 55% yield).

Ή NMR (DMSO-iM): 8.87 (0.7 Η, s), 8.62 (0.3 Η, s), 7.80 (1 Η, m), 4.44 (0.7 Η, dd, J = 11.9, 8.5 Hz), 4.29 (0.7 H, qd, J = 8.2, 2.9 Hz), 4.21 (0.3 H, m), 3.93 (0.6 H, m), 3.71 (1 H, m), 3.55 (1 H, m), 3.45 (0.3 H, dd, J = 10.5, 3.7 Hz), 3.39 (0.7 H, m), 3.12 (0.7 H, dd, J = 11.7, 8.9 Hz), 2.18 (1 H, m), 2.06 (0.7 H, m), 1.73 (0.3 H, m).

1 ³ C NMR (DMSO-iM): 186.5, 186.3, 146.4, 146.3, 146.2, 145.2, 145.1, 144.8, 144.7, 144.6, 143.6, 143.5, 121.5, 121.4, 121.3, 120.9, 120.8, 120.7, 105.4, 105.3, 105.2, 105.2, 105.1, 105.0, 62.7, 60.8, 52.2, 51.1, 47.4, 36.6, 35.9, 34.2, 31.7.

Example 112: (5)-6-(2,3,6-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[ l,2-c]imidazole-3- thione

Compound was prepared in an analogous manner to Example 59 from (E)-2,3,6-trifluoro-5-(2- nitrovinyl)benzene using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63 0) and isolated as a light khaki powder.

Ή NMR (DMSO-iM): 11.85 (1 H, br s), 7.47 (1 H, qd, J = 9.5, 4.9 Hz), 7.18 (1 H, tdd, J = 9.6, 9.6, 3.8, 1.9 Hz), 6.63 (1 H, d, J = 1.9 Hz), 4.49 (1 H, quin, J = 8.6 Hz), 4.19 (1 H, dd, J = 11.3, 9.4 Hz), 3.75 (1 H, dd, J = 11.6, 7.8 Hz), 3.32 (1 H, dd, J = 15.9, 9.3 Hz), 2.94 (1 H, dd, J = 15.9, 7.8 Hz).

¹³ C NMR (DMSC M): 157.0, 156.9, 155.9, 155.4, 155.3, 155.3, 155.3, 149.1, 149.1, 149.0, 149.0, 147.6, 147.5, 147.5, 147.4, 147.4, 147.3, 146, 145.9, 145.9, 145.9, 132.2, 119, 118.9, 118.9, 118.8, 116.5, 116.5, 116.4, 116.3, 112.0, 112.0, 112.0, 111.9, 111.8, 111.8, 111.8, 111.8, 106.6, 48.5, 35.7, 29.5.

Example 113: ( ?)-6-(2,3,6-trifluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo[l ,2-c]imidazole-3- thione

Compound was prepared in an analogous manner to Example 58 from (E)-2,3,6-trifluoro-5-(2- nitrovinyl)benzene using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7) and isolated as a light khaki powder. Ή NMR (DMSO-iM): 11.84 (1 Η, br s), 7.46 (1 Η, qd, J = 9.5, 5.1 Hz), 7.17 (1 H, ddt, J = 1.9, 3.9, 9.8 Hz ), 6.62 (1 H, d, J = 2.1 Hz), 4.48 (1 H, quin, J = 8.6 Hz), 4.17 (1 H, dd, J = 11.3, 9.4 Hz), 3.74 (1 H, dd, J = 11.6, 7.9 Hz), 3.31 (1 H, dd, J = 9.6, 16 Hz), 2.93 (1 H, dd, J = 15.8, 7.9 Hz). ¹³ C NMR (DMSO-<ft5): 157, 157, 156.9, 156.9, 155.9, 155.4, 155.4, 155.3, 155.3, 149.1, 149.1, 149, 149, 147.6, 147.6, 147.5, 147.4, 147.4, 147.3, 146, 146, 145.9, 145.9, 132.2, 119, 118.9, 118.9, 118.8, 116.5, 116.5, 116.4, 116.3, 112, 112, 112, 112, 111.9, 111.8, 111.8, 111.8, 106.6, 48.5, 35.7, 29.5.

Example 114: ( ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahydro -3H-pyrrolo[l,2- c]imidazole-3-thione

Step 1: (4R)-4-(2,3,5, -tetrafluorophenyl)pyrrolidine-2-carboxylic acid

A suspension of (4 ?)-l-(ieri-butoxycarbonyl)-4-(2,3,5,6-tetrafluorophenyl)pyrr olidine-2- carboxylic acid (0.45 g, 1.239 mmol) (analogous to Example 58 step 10) in 2 M HCI (9.29 mL, 18.58 mmol) was stirred under reflux for 2 h. Thereupon, the mixture was concentrated under vacuum, the residue was dissolved in water, and then pH was adjusted to 7 with 5 M sodium hydroxide. The resulting precipitate was collected, washed with water and dried to give (4R)-4- (2,3,5,6-tetrafluorophenyl)pyrrolidine-2-carboxylic acid as an off-white powder (0.2 g, 61% yield).

Step 2: (6R)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-3-thioxohexahydr o-lH-pyrrolo[l,2- c ]imidazol-l - ne

To a solution of (4 ?)-4-(2,3,5,6-tetrafluorophenyl)pyrrolidine-2-carboxylic acid (0.18 g, 0.684 mmol) in 0.5 M sodium carbonate (10.94 mL, 5.47 mmol) and dioxane (11 mL) was added methyl isothiocyanate (0.100 g, 1.368 mmol). The mixture was stirred for 1 h at room temperature, then heated at 50-60 °C to give clear solution. Thereupon, the reaction was allowed to cool down naturally to room temperature, and then acidified to pH = 1-2 by adding cc HCI. The reaction was heated under reflux for 1 h, and then evaporate to ca. 5 mL of volume and the separated oily product crystallised on standing. Thereupon, the mixture was diluted with water (10 mL), stirred at 0-5 °C for 30 min, the resulting solid was collected, washed with water and dried under vacuum to give (6 ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-3-thioxohexahydro- lH- pyrrolo[l,2-c]imidazol- l-one as a light cream powder (0.20 g, 92% yield).

Step 3: ( ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-2,5,6,7-tetrahydro -3H-pyrrolo[l,2- c]imidazol -3-thione

To a solution of (6 ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-3-thioxohexahydro- lH-pyrrolo[l,2- c]imidazol- l-one (0.17 g, 0.534 mmol) in dry tetrahydrofuran (3 mL) was added 65% RED-A1 (bis(2-methoxyethoxy)aluminum(III) sodium hydride) (0.104 mL, 0.347 mmol) in toluene dropwise at 0-5 °C under nitrogen and the mixture was allowed to stir in the cold for 30 min. Thereupon, the mixture was quenched with cc HCl (0.445 mL, 5.34 mmol), and allowed to warm up naturally room temperature and stirred for 1 h. The solvents were then evaporated off, and the residue was taken up in ethyl acetate. The organic phase was dried over MgS0 ₄ , filtered, and evaporated to dryness. Chromatography (petroleum ether - ethyl acetate; 2: 1, then 1 : 1) afforded ( ?)-2-methyl-6-(2,3,5,6-tetrafluorophenyl)-6,7-dihydro-2H-pyr rolo[l,2-c]imidazole-3(5H)- thione as a white powder (0.094 g, 58% yield).

Ή NMR (DMSO-iM): 7.86 (1 Η, m), 6.88 (1 Η, s), 4.52 (1 Η, quin, J = 8.4 Hz), 4.23 (1 H, dd, J = 11.4, 9.5 Hz), 3.83 (1 H, dd, J = 11.7, 7.5 Hz), 3.36 (1 H, dd, J = 9.4, 16.1 Hz), 3.34 (3 H, s), 2.99 (l H, dd, J = 16.1, 7.6 Hz).

¹³ C NMR (DMSO-iM): 156.5, 146.4, 146.4, 146.3, 146.3, 146.2, 145.3, 145.3, 145.3, 145.3, 145.3, 145.2, 145.2, 145.2, 144.8, 144.8, 144.7, 144.7, 144.7, 144.6, 144.6, 143.7, 143.7, 143.7, 143.6, 143.6, 143.6, 130.4, 120.6, 120.5, 120.4, 110.8, 105.9, 105.7, 105.6, 49.3, 35, 34.1, 29.4. Example 115: (5a5,6a/?)-5a-(3-bromo-2,6-difluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

Compound was prepared in an analogous manner to Example 53 from 2-(3-bromo-2,6- difluorophenyl)acetonitrile and ( ?)-2-(chloromethyl)oxirane and isolated as a white solid.

Ή NMR (DMSO-df5): 11.78 (1 H, s), 7.74 (1 H, td, J = 8.4, 5.9 Hz), 7.16 (1 H, dt, J = 1, 9.2 Hz), 6.71 (1 H, d, J = 2.2 Hz), 4.05 (1 H, d, J = 12.2 Hz), 3.75 (1 H, d, J = 12.2 Hz), 2.75 (1 H, dd, J = 8.4, 4.4 Hz), 1.69 (1 H, dd, J = 8.3, 5.6 Hz), 1.29 (1 H, t, J = 4.9 Hz) .

¹³ C NMR (DMSO-df5): 162, 161.9, 160.3, 160.3, 158.9, 158.8, 157.2, 157.2, 156.6, 134.4, 133.1, 133.1, 117.1, 117, 116.8, 113.5, 113.5, 113.4, 113.4, 106.6, 103.8, 103.7, 103.6, 103.6, 51.4, 26.8, 21.8, 21.6.

Example 116: (5aS,6a ?)-5a-(5-chloro-2-fluorophenyl)-2-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrro -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 114 from (lR,5S)-3-(tert- butoxycarbonyl)-5-(5-chloro-2-fluorophenyl)-3-azabicyclo[3.1 .0]hexane-2-carboxylic acid and isolated as a light beige solid.

Ή NMR (DMSO- 6): 7.50 (1 Η, dd, J = 6.5, 2.7 Hz), 7.43 (1 H, ddd, J = 8.8, 4.4, 2.7 Hz), 7.30 (1 H, dd, J = 9.9, 8.9 Hz), 6.93 (1 H, s), 4.13 (1 H, d, J = 11.9 Hz), 3.84 (1 H, d, J = 12.0 Hz), 2.92 (1 H, dd, J = 8.4, 4.2 Hz), 1.69 (1 H, dd, J = 8.4, 5.4 Hz), 1.17 (1 H, t, J = 4.8 Hz) .

1 ³ C NMR (DMSO-df5): 161.3, 159.7, 157.2, 132.9, 130.2, 130.2, 129.4, 129.4, 128.7, 128.6, 128.3, 128.3, 117.6, 117.4, 110.4, 52.3, 52.3, 34.1, 31.9, 22.1, 20.9. Example 117: (5)-6-(3-bromo-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyr rolo[l,2- c]imidazole-3-thione

(E)-l-bromo-2,4-difluoro-3-(2-nitrovinyl)benzene (using 4-(( ?)-hydroxy((15,25,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0)) was converted to (5)- 6-(3-bromo-2,6-dilluorophenyl)-2,5,6,7-tetrahydro-3H-pyrrolo [l,2-c]imidazole-3-thione by a similar procedure as described for Example 59 and the product was isolated as a light khaki powder.

Ή NMR (DMSO-iM): 11.85 (1 Η, br s), 7.72 (1 Η, ddd, J = 8.9, 8.1, 5.8 Hz), 7.16 (1 H, t, J = 9.4 Hz), 6.63 (1 H, s), 4.50 (1 H, quin, J = 8.5 Hz), 4.17 (1 H, dd, J = 11.5, 9.3 Hz), 3.74 (1 H, dd, J = 11.7, 7.7 Hz), 3.31 (1 H, dd, J = 16.1, 9.5 Hz), 2.92 (1 H, dd, J = 15.9, 7.8 Hz).

1 ³ C NMR (DMSO-iM): 160.8, 160.8, 159.2, 159.1, 157.6, 157.5, 155.9, 155.9, 155.8, 132.5, 132.4, 132.3, 118.9, 118.8, 118.6, 113.8, 113.8, 113.6, 113.6, 106.6, 104.1, 104.1, 103.9, 103.9, 48.6, 35.7, 29.5.

Example 118: ( ?)-6-(3-bromo-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyrr olo[l,2- c]imidazole-3-thione

(E)-3-bromo-2,6-difluoro-5-(2-nitrovinyl)benzene (using 4-((5)-hydroxy((15,2 ?,45,5 ?)-5- vinylquinuclidin-2-yl)methyl)quinolin-6-ol as catalyst (CAS # 70877-75-7)) was converted to ( ?)-6-(3-bromo-2,6-difluorophenyl)-2,5,6,7-tetrahydro-3H-pyrr olo[l,2-c]imidazole-3-thione by a similar procedure as described for Example 58 and the product was isolated as a light beige powder. Ή NMR (DMSO-ίΜ): 11.85 (1 H, br s), 7.72 (1 H, ddd, J = 8.9, 8.1, 5.8 Hz), 7.16 (1 H, t, J = 9.4 Hz), 6.63 (1 H, s), 4.50 (1 H, quin, J = 8.5 Hz), 4.17 (1 H, dd, J = 11.5, 9.3 Hz), 3.74 (1 H, dd, J = 11.7, 7.7 Hz), 3.31 (1 H, dd, J = 16.1, 9.5 Hz), 2.92 (1 H, dd, J = 15.9, 7.8 Hz).

1 ³ C NMR (DMSC M): 160.8, 160.8, 159.2, 159.1, 157.6, 157.5, 155.9, 155.9, 155.8, 132.5, 132.4, 132.3, 118.9, 118.8, 118.6, 113.8, 113.8, 113.6, 113.6, 106.6, 104.1, 104.1, 103.9, 103.9, 48.6, 35.7, 29.5.

Example 119: (5aS,6a/?)-5a-(3-bromo-2,6-difluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo 2, 1 -c] [l,2,4]triazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 60 from tert-butyl (((15,2 ?)-l-(3- bromo-2,6-difluorophenyl)-2-(hydroxymethyl)cyclopropyl)methy l)carbamate and isolated as a pink solid.

Ή NMR (DMSO-iM): 13.29 (1 Η, s), 7.78 (1 Η, td, J = 8.5, 5.9 Hz), 7.18 (1 H, td, J = 9.2, 1.3 Hz), 4.12 (1 H, d, J = 12.2 Hz), 3.85 (1 H, d, J = 12.2 Hz), 2.94 (1 H, dd, J = 8.8, 4.3 Hz), 1.81 (1 H, dd, J = 8.8, 5.9 Hz), 1.67 (1 H, d, J = 4.7 Hz).

¹³ C NMR (DMSC M): 163.6, 161.8, 161.8, 160.2, 160.2, 158.8, 158.7, 157.6, 157.1, 157.1, 133.5, 133.5, 116.1, 116.0, 115.9, 113.6, 113.5, 113.4, 113.4, 103.8, 103.8, 103.6, 103.6, 49.5, 27.4, 20.1, 19.7.

Example 120: (5aS,6a ?)-5a-(5-bromo-2-fluorophenyl)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo 2,l-c][l,2,4]triazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 60 from tert-butyl (((lS,2 ?)-l-(5- bromo-2-fluorophenyl)-2-(hydroxymethyl)cyclopropyl)methyl)ca rbamate and isolated as a pale brown solid.

Ή NMR (DMSO-df5): 7.69 (1 H, dd, J = 6.7, 2.5 Hz), 7.58 (1 H, ddd, J = 8.8, 4.5, 2.6 Hz), 7.26 (1 H, dd, J = 10.0, 8.8 Hz), 4.15 (1 H, d, J = 11.9 Hz), 3.87 (1 H, d, J = 11.9 Hz), 3.08 (1 H, dd, J = 8.9, 4.0 Hz), 1.78 (1 H, dd, J = 8.7, 5.6 Hz), 1.51 (1 H, dd, J = 4.3, 5.5 Hz).

1 ³ C NMR (DMSO-df5): 163.6, 161.8, 160.1, 157.9, 133.2, 133.2, 132.7, 132.7, 128.3, 128.1, 118.0, 117.9, 116.2, 49.7, 33, 20.6, 19.1. Example 121: (5a5,6a ?)-5a-(3-bromo-2,6-difluorophenyl)-l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l, -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 80 from 2-(5-bromo-2,6- difluorophenyl)acetonitrile and (7?)-2-(chloromethyl)oxirane and isolated as a white solid.

Ή NMR (DMSO-df5): 11.68 (1 Η, br s), 7.74 (1 Η, td, J = 8.4, 5.9 Hz), 7.15 (1 H, td, J = 9.2, 1.2 Hz), 4.01 (1 H, d, J = 12.3 Hz), 3.71 (1 H, d, J = 12.0 Hz), 2.72 (1 H, dd, J = 8.3, 4.5 Hz), 2.05 (3 H, s), 1.65 (1 H, dd, J = 8.2, 5.6 Hz), 1.25 (1 H, t, J = 5.0 Hz).

¹³ C NMR(DMSO-df5): 161.9, 161.9, 160.3, 160.2, 158.8, 158.8, 157.2, 157.1, 155.7, 133.0, 133.0, 130.0, 117.2, 117.1, 115.1, 113.5, 113.3, 103.7, 103.7, 103.6, 51.4, 26.5, 21.8, 20.9, 9.4.

Example 122: (5aS,6a/?)-5a-(5-bromo-2-fluorophenyl)-l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l, -c]imidazole-3(2H)-thione

Step 1: ((lR,2S)-2-(aminomethyl)-2-(5-bromo-2-fluorophenyl)cycloprop yl)methanol

To a stirred solution of 2-(5-bromo-2-fluorophenyl)acetonitrile (10 g, 46.7 mmol) in dry tetrahydrofuran (100 mL), was added ( ?)-2-(chloromethyl)oxirane (4.38 mL, 56.1 mmol) at room temperature, under inert atmosphere, The reaction was then cooled to 0° C and 2 M sodium bis(trimethylsilyl)amide in tetrahydrofuran (40.9 mL, 82 mmol) was added dropwise keeping the temperature between 0-5 °C. Thereupon, the obtained red mixture was allowed to warm up to room temperature and stirred for 3 h. The reaction was diluted with dry tetrahydrofuran (100 mL), cooled to 0 °C and sodium borohydride (7.07 g, 187 mmol) was added, followed by dropwise addition of boron trifluoride etherate (23.68 mL, 187 mmol). The mixture was allowed to warm to room temperature naturally and stirred overnight. The obtained pale yellow suspension was then cooled to 0 °C and carefully quenched with 2 M HC1 ( 140 ml, 280 mmol). The tetrahydrofuran was evaporated off under vacuum, the aqueous phase was washed with diethyl ether (discarded), then was basified to pH = 10 (3 M NaOH) and extracted with dichloromethane. The organic phase was dried over MgSC , filtered and evaporated to leave a yellow oil. Yield: 11.75 g, 73 %.

Step 2: tert-butyl (((lS,2R)-l-(5-bromo-2-fluorophenyl)-2- (hydroxymethyl)cyclopropyl)methyl)carbamate

To an ice-cooled solution of ((1 ?,25)-2-(aminomethyl)-2-(5-bromo-2- fluorophenyl)cyclopropyl)methanol (11.75 g, 42.9 mmol) in ethanol (145 mL), was added di- tert-buty\ dicarbonate (9.35 g, 42.9 mmol). The solution was stirred at room temperature for 4 h. Then the solvent was evaporated and the residue was separated on a column. The titled compound was isolated as a yellow foam. Yield: 10.1 g, 56 %.

Step 3: tert-butyl (lS,5R)-l-(5-bromo-2-fluorophenyl)-4-hydroxy-3-az bicyclo[3.1.0]hexane-3- carboxylate

To a stirred solution of oxalyl dichloride (2.60 mL, 29.7 mmol) in dry dichloro methane (62.8 mL), was added dropwise a solution of DMSO (4.21 mL, 59.4 mmol) in dry dichloromethane (12.5 mL) at -78 °C over 30 min. The reaction mixture was stirred for 5 min in the cold, and then a solution of tert-bvXy\ ((( \S,2R)- l-(5-bromo-2-fluorophenyl)-2-

(hydroxymethyl)cyclopropyl)methyl)carbamate (10.1 g, 27.0 mmol) in dry dichloromethane (25 mL) was added, dropwise over 30 min. The mixture was stirred at -78 °C for 1 h, and then triethylamine (18.8 mL, 135 mmol) was added. The reaction was allowed to warm up gradually to room temperature and stirred for 2 h. Thereupon the mixture was washed three times with water, dried over MgSC , filtered and evaporated to give a yellow oil. Yield: 10.1 g, 85 %.

Step 4: tert-butyl (lS,5R)-l-(5-bromo-2-fluorophenyl)-4-cyano-3-azabicyclo[3.1. 0]hexane-3- carboxylate

To a stirred solution of tert-butyl (15,5 ?)-l-(5-bromo-2-fluorophenyl)-4-hydroxy-3- azabicyclo[3.1.0]hexane-3-carboxylate (10.1 g, 27.1 mmol) in dry dichloromethane (133 mL) was added trimethylsilanecarbonitrile (9.71 mL, 72.4 mmol) at room temperature under inert atmosphere. Then, the solution was cooled to -78 °C and boron trifluoride diethyl etherate (10.08 mL, 80.0 mmol) was added dropwise. The reaction mixture was stirred at -78 °C for 4 h., and then saturated solution of NaHC0 ₃ was added and the mixture was allowed to warm to room temperature. The organic phase was separated and aqueous phase was extracted with dichloromethane. The combined organic phases were dried over MgSC , filtered and evaporated to give 10.3 g of yellow oil. Yield: 85 %.

Step 5: (lR,5S)-5-(5-bromo-2-fluorophenyl)-3-(tert-butoxycarbonyl)-3 -azabicyclo[3.1.0]hexane- 2-carboxylic acid

To a stirred solution of tert-butyl ( IS,5R)- l-(5-bromo-2-fluorophenyl)-4-cyano-3- azabicyclo[3.1.0]hexane-3-carboxylate (10.3 g, 27.0 mmol) in ethanol (93 mL), at room temperature was added a solution of 3 M NaOH (45 mL, 135 mmol). The solution was heated at 80 °C for 3 h. Then, the reaction was cooled to room temperature, ethanol was evaporated and the aq. phase was acidified with 2N HCl solution, the resulting solid was filtered off, dissolved in a mixture of dichloromethane - isopropanol (7:3). The organic phase was dried over MgS04, filtered and evaporated to give the titled product as a yellow semi-solid. Yield: 10.5 g, 78 %. Step 6: tert-butyl (lS,5R)-l-(5-bromo-2-fluorophenyl)-4-(methoxy(methyl)carbamo yl)-3- azabicyclo[3.1.0]hexane-3-carboxylate

To a stirred solution of ((lR,5S)-5-(5-bromo-2-fluorophenyl)-3-(tert-butoxycarbonyl)- 3- azabicyclo[3.1.0]hexane-2-carboxylic acid (2.5 g, 6.25 mmol) in anhydrous dichloromethane (36 mL) was added di(lH-imidazol-l-yl)methanone (1.215 g, 7.50 mmol) portion wise under nitrogen and the reaction stirred for 30 min. Thereupon, N,0-dimethylhydroxylamine hydrochloride (0.731 g, 7.50 mmol) was added and the mixture was stirred overnight. The reaction mixture was then diluted with dichloromethane (ca. to 60 mL) and washed with water. The organic phase was dried over MgS04, filtered and evaporated to give the titled product as a yellow yellow oil. Yield: 1.57 g, 45 %.

Step 7: tert-butyl (lS,5R)-4-acetyl-l-(5-bromo-2-fluorophenyl)-3-az bicyclo[3.1.0]hexane-3- carboxylate

To a stirred solution of (lS,5R)-tert-butyl l-(5-bromo-2-fluorophenyl)-4- (methoxy(methyl)carbamoyl)-3-azabicyclo[3.1.0]hexane-3-carbo xylate (1.57 g, 3.54 mmol) in anhydrous tetrahydrofuran (15 mL) was added methylmagnesium iodide (3.54 ml, 10.62 mmol) dropwise at 0 °C. The reaction mixture was stirred in the cold for 1 h, and then quenched by addition of 1 M HCl (14.17 ml, 14.17 mmol). The mixture was extracted with a mixture of ethyl acetate - petroleum ether (1: 1). The organic phase was washed with brine, dried over MgSC , filtered and evaporated to give 1.34 g of yellow oil. Yield: 86 %.

Step 8: l-((lR,5S)-5-(5-bromo-2-fluorophenyl)-3-az bicyclo[3.1.0]hexan-2-yl)ethan-l-one hydrochlori

To a stirred solution of {\S,5R)-tert-buty\ 4-acetyl-l-(5-bromo-2-fluorophenyl)-3- azabicyclo[3.1.0]hexane-3-carboxylate (1.33 g, 3.34 mmol) was added 4 M HCl in dioxane (6.68 mL, 26.7 mmol) and then the mixture was stirred at room temperature for 2 h. Thereupon, diethyl ether was added and the mixture was evaporated to dryness to give an orange oil. Yield: 1.2 g, 91 %.

Step 9: ( 5aS,6aR)-5a-( 5-bromo-2-fluorophenyl)-l -methyl-5,5a, 6, 6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

To a stirred solution of l-((1 ?,55)-5-(5-bromo-2-fluorophenyl)-3-azabicyclo[3.1.0]hexan-2- yl)ethanone hydrochloride (1.1 g, 3.29 mmol) in a mixture of ethanol (13.5 mL) and water (13.5 mL) was added potassium thiocyanate (0.351 g, 3.62 mmol) followed by addition of cc. HCl (0.135 mL, 1.644 mmol). The solution was heated at reflux for 1 h. The reaction was cooled to room temperature, and then ethanol was removed. The aqueous phase was extracted with dichloromethane, the organic phase was dried over MgSC , filtered and evaporated. Chromatography in a mixture of dichloromethane - methanol afforded the titled compound as a beige foam. Yield: 0.9 g, 77 %. Ή NMR (DMSO-ίΜ): 11.65 (1 H, s), 7.59 (1 H, dd, J=6.7, 2.5 Hz), 7.55 (1 H, ddd, J=8.7, 4.5, 2.6 Hz), 7.24 (1 H, dd, J=10.1, 8.7 Hz), 4.05 (1 H, d, J=12.0 Hz), 3.76 (1 H, d, J=12.0 Hz), 2.87 (1 H, dd, J=8.3, 4.3 Hz), 2.04 (3 H, s), 1.64 (1 H, dd, J=8.2, 5.3 Hz), 1.12 (1 H, t, J=4.8 Hz). ¹³ C NMR (DMSO-iM): 161.8, 160.2, 155.7, 132.9, 132.9, 132.3, 132.2, 130.2, 129.4, 129.3, 118, 117.8, 116.2, 1 16.2, 114.8, 51.5, 51.5, 32.2, 22.2, 20.2, 9.3.

Example 123: (5a5,6a ?)-5a-(3-chloro-2,6-difluorophenyl)- l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l, -c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 122 from 2-(3-chloro-2,6- difluorophenyl)acetonitrile. The product was isolated as a beige solid.

Ή NMR (DMSO-iM): 11.68 (1 Η, s), 7.63 (1 Η, td, J=8.6, 5.8 Hz), 7.21 (1 H, t, J=8.6 Hz), 4.01 (1 H, d, J=12.2 Hz), 3.72 (1 H, d, J=12.2 Hz), 2.73 (1 H, dd, J=8.2, 4.4 Hz), 2.05 (3 H, s), 1.65 (1 H, dd, J=8.2, 5.6 Hz), 1.25 (1 H, t, J=5.0 Hz).

1 ³ C NMR (DMSO-iM): 161.2, 161.2, 159.6, 159.6, 157.8, 157.8, 156.2, 156.1, 155.7, 130.3, 130.2, 129.9, 117.2, 117.1, 117, 115.7, 115.7, 115.6, 115.6, 115.1, 112.9, 112.9, 112.8, 112.8, 51.4, 26.4, 21.7, 20.8, 9.4.

Example 124: ( ?)-6-(3-bromo-2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 129 from 3-bromo-2,6- difluorobenzaldehyde and isolated as a beige powder.

Ή NMR (DMSO-iM): 11.73 (1 H, br s), 7.72 (1 H, ddd, J=8.9, 8.1, 5.8 Hz), 7.16 (1 H, m), 4.44 (1 H, quin, J=8.6 Hz), 4.13 (1 H, dd, J=11.5, 9.2 Hz), 3.71 (1 H, dd, J=11.6, 7.9 Hz), 3.23 (1 H, dd, J=15.5, 9.3 Hz), 2.84 (1 H, dd, J=15.4, 8.1 Hz), 1.97 (3 H, s).

¹³ C NMR (DMSO-iM): 160.8, 160.8, 159.2, 159.1, 157.5, 157.5, 155.9, 155.8, 155, 132.4, 132.4, 127.7, 118.8, 118.7, 118.6, 115.1, 113.8, 113.8, 113.6, 113.6, 104.1, 104, 103.9, 103.9, 48.5, 35.8, 28.7, 9.3. Example 125: (5)-6-(3-bromo-2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 129 from 3-bromo-2,6- difluorobenzaldehyde using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0) and isolated as a beige powder.

Ή NMR (DMSO-iM): 11.72 (1 Η, br s), 7.72 (1 Η, ddd, J=8.9, 8.1, 5.8 Hz), 7.16 (1 H, m), 4.44 (1 H, t, J=8.7 Hz), 4.13 (1 H, dd, J=11.5, 9.2 Hz), 3.71 (1 H, dd, J=11.6, 7.9 Hz), 3.23 (1 H, dd, J=15.5, 9.3 Hz), 2.84 (1 H, dd, J=15.5, 8.1 Hz), 1.97 (3 H, s).

¹³ C NMR (DMSO-iM): 160.8, 160.8, 159.2, 159.1, 157.5, 157.5, 155.9, 155.8, 155, 132.4, 132.4, 127.7, 118.8, 118.7, 118.6, 115.1, 113.8, 113.8, 113.6, 113.6, 104.1, 104, 103.9, 103.9, 48.5, 35.8, 28.7, 9.3.

Example 126: (5a5,6a ?)-5a-(3-chloro-5-fluorophenyl)- l-methyl-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo[l,2-c]imidazole-3(2H)-thion e

Compound was prepared in an analogous manner to Example 122 from 2-(3-chloro-5- fluorophenyl)acetonitrile. The product was isolated as a beige solid.

Ή NMR (DMSO-df5): 11.64 (1 H, s), 7.30 (1 H, dt, J=8.7, 2.1 Hz), 7.28 (1 H, t, J=1.6 Hz), 7.23 (1 H, dt, J=10.0, 1.8 Hz), 4.19 (1 H, d, J=12.2 Hz), 3.99 (1 H, d, J=12.0 Hz), 3.00 (1 H, dd, J=8.3, 4.3 Hz), 2.03 (3 H, s), 1.64 (1 H, dd, J=8.3, 5.2 Hz), 1.14 (1 H, t, J=4.8 Hz).

1 ³ C NMR DMSO-d6): 163.1, 161.4, 156, 145, 144.9, 134.1, 134.1, 130.2, 123, 123, 114.5, 114.3, 114.1, 112.9, 112.8, 50.8, 36, 36, 25.2, 22.2, 9.3. Example 127: (5a5,6a ?)-5a-(5-bromo-2-fluorophenyl)-l-(methyl-<i3)-5,5a,6,6a- tetrahydrocyclopropa[3,4]pyrrolo l,2-c]imidazole-3(2H)-thione

Compound was prepared in an analogous manner to Example 122 from 2-(5-bromo-2- fluorophenyl)acetonitrile. The product was isolated as a beige solid.

Ή NMR (DMSO-df5): 11.65 (1 Η, s), 7.59 (1 Η, dd, J=6.7, 2.6 Hz), 7.55 (1 H, ddd, J=8.7, 4.5, 2.6 Hz), 7.23 (1 H, dd, J=10.1, 8.7 Hz), 4.05 (1 H, d, J=12.0 Hz), 3.76 (1 H, d, J=12.0 Hz), 2.87 (1 H, dd, J=8.2, 4.3 Hz), 1.64 (1 H, dd, J=8.3, 5.4 Hz), 1.12 (1 H, t, J=4.8 Hz).

1 ³ C NMR (DMSO-<i<5): 161.8, 160.2, 155.7, 132.9, 132.9, 132.3, 132.2, 130.3, 129.4, 129.3, 118, 117.8, 116.2, 116.2, 114.7, 51.5, 51.5, 32.3, 22.2, 20.2. Example 128: (5)-6-(5-bromo-2-fluorophenyl)-l-methyl-2,5,6,7-tetrahydro-3 H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 129 from 5-bromo-2- fluorobenzaldehyde using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0) and isolated as an off-white solid.

Ή NMR(DMSO-iM): 11.70 (1 Η, br s), 7.58 (1 Η, dd, J=6.7, 2.5 Hz), 7.53 (1 H, ddd, J=8.7, 4.5, 2.5 Hz), 7.23 (1 H, dd, J=10.3, 8.8 Hz), 4.20 (1 H, quin, J=8.1 Hz), 4.11 (1 H, dd, J=10.9, 8.1 Hz), 3.71 (1 H, dd, J=11.3, 7.9 Hz), 3.18 (1 H, dd, J=15.2, 8.1 Hz), 2.85 (1 H, ddd, J=15.2, 8.3, 1.2 Hz), 1.98 (3 H, s).

¹³ C NMR(DMSO-iM): 160.3, 158.7, 155.1, 131.8, 131.8, 131.4, 131.4, 130.6, 130.5, 127.5, 118, 117.9, 116.5, 116.4, 115.4, 49, 40.5, 29, 9.3.

Example 129: ( ?)-l-methyl-6-(2,3,6-trifluorophenyl)-6,7-dihydro-2H-pyrrolo [l,2-c]imidazole- 3(5H)-thione

Step 1: (E)-l,2, -trifluoro-3-(2-nitrovinyl)benzene

To a solution of methanol (90 mL) and 1.5 M sodium hydroxide (131 mL, 197 mmol) was added a solution of 2,3,6-trifluorobenzaldehyde (30 g, 187 mmol) and nitromethane (16 mL, 299 mmol) in methanol (60 mL) dropwise over 40 min at 5 °C, while the internal temperature was maintained between 5 and 10 °C with external cooling. The reaction was then agitated in the cold for 30 min., and then a solution of acetic acid (16 mL, 281 mmol) was added in one portion at 0- 10 °C with stirring. The resulting mixture extracted with dichloro methane (ca. 200 mL), the organic phase was washed with brine, dried (MgS0 ₄ ), filtered to give l-(3-bromo-2,6- difluorophenyl)-2-nitroethanol solution in dichloromethane. Thereupon, the above solution (ca. 270 mL) was treated with N,N-dimethylpyridin-4-amine (2.289 g, 18.74 mmol) followed by addition of acetic anhydride (21.26 ml, 225 mmol) and the mixture was stirred at room temperature overnight. The reaction mixture was then washed with water and sodium bicarbonate solution, respectively. The organic phase was dried over MgS04, filtered and evaporated to dryness. The crude product was crystallized from a mixture of isopropanol and water to give a light brownish solid. Yield: 38.1 g, 88 %.

Step 2: ethyl (R)-2-(2-nitro-l-(2,3,6-trifluorophenyl)ethyl)malonate

To a cold solution of (E)-l,2,4-trifluoro-3-(2-nitrovinyl)benzene (5 g, 24.62 mmol) and l-(3,5- bis(trifluoromethyl)phenyl)-3-((1 ?,2 ?)-2-(dimethylamino)cyclohexyl)thiourea (CAS # 620960- 26-1) (0.305 g, 0.738 mmol) in dry toluene (40 ml) was added diethyl malonate (4.88 mL, 32.0 mmol) and the solution was kept for 16 h at -20 °C (in the freezer), the reaction was then warmed up to room temperature, washed with 30 mL of 1 M HC1 solution, dried over MgS0 ₄ , filtered through a silica pad and evaporated to dryness to give ( ?)-diethyl 2-(2-nitro-l-(2,3,6- trifluorophenyl)ethyl)malonate as a yellowish oil. Yield: 10.3 g, 98 %.

Step 3: ethyl (4R)- -oxo-4-(2,3,5-trifluorophenyl)pyrrolidine-3-carboxylate

To a suspension of (K)-diethyl 2-(2-nitro-l-(2,3,6-trifluorophenyl)ethyl)malonate (10.3 g, 22.68 mmol) in methanol (115 mL) was added nickel(II) chloride hexahydrate (5.39 g, 22.68 mmol) followed by addition of sodium borohydride (6.86 g, 181 mmol) in portions with ice cooling over 30 min. The mixture was stirred for 5 h at room temperature, then quenched with 2 M HCl solution (60 mL) followed by addition of cc. ammonia (5 mL). The mixture was then diluted with dichloro methane (150 mL), acidified with 6 M HCl to pH=2, and stirred for 16 h to give a clear solution. Thereupon, the mixture was extracted with dichloromethane, the organic phase was dried over MgSC , filtered and evaporated to dryness. Crystallization from petroleum ether gave the titled product as a light beige powder. (Yield: 6.19 g, 95 %).

Step 4: (4R)-2-oxo-4- -trifluorophenyl)pyrrolidine-3-carboxylic acid

To a stirred solution (4R)-ethyl 2-oxo-4-(2,3,6-trifluorophenyl)pyrrolidine-3-carboxylate (6 g, 20.89 mmol) in ethanol (90 mL) was added 1 M sodium hydroxide (25.1 mL, 25.1 mmol). The resulting suspension was stirred for 2 h at room temperature, the organics were then removed under vacuum, and the residue was dissolved in water (50 mL). The product was crystallized on acidification with 6 M HCl. The resulting crystals were collected, washed with cold water and dried under vacuum at 50 °C to give the product as a beige powder. Yield: 4.75 g, 88 %.

Step 5: (R)-4-(2,3,5-trifluorophenyl)pyrrolidin-2-one

A solution of (4R)-2-oxo-4-(2,3,6-trifluorophenyl)pyrrolidine-3-carboxylic acid (4.64 g, 17.90 mmol) in toluene (150 mL) was stirred under reflux for 3 h, thereupon, the mixture was evaporated to 30 mL followed by addition of petroleum ether afforded the titled product as a beige powder. Yield: 3.45 g, 90 %.

Step 6: tert-butyl (R)-2-oxo-4-(2,3,5-trifluorophenyl)pyrrolidine-l-carboxylate

To a stirred solution of ( ?)-4-(2,3,6-trifluorophenyl)pyrrolidin-2-one (3.35 g, 15.57 mmol)) in dry dichloro methane (14 mL) was added at room temperature di-ie/t-butyl dicarbonate (5.10 g, 23.35 mmol) followed by addition of N,N-dimethylpyridin-4-amine (1.902 g, 15.57 mmol). The mixture was then stirred at room temperature for 24 h at room temperature, and then diluted with dichloromethane to 80 mL washed with 10 % citric acid (80 mL). The organic phase was dried (MgS0 ₄ ), filtered through silica pad, and then the filtrate was evaporated to dryness. Crystallization from petroleum ether afforded (R)-te rt-butyl 2-oxo-4-(2,3,6- trifluorophenyl)pyrrolidine-l-carboxylate as an off-white powder. Yield: 4.15 g, 85 %.

Step 7: tert-butyl (4R)-2-hydroxy-4-(2,3,5-trifluorophenyl)pyrrolidine-l-carbox ylate

To a stirred solution of (R) -tert-butyl 2-oxo-4-(2,3,6-trifluorophenyl)pyrrolidine-l-carboxylate (4 g, 12.69 mmol) in a mixture of dry diethyl ether (39 mL) and tetrahydrofuran (13 mL) was added dropwise 65 % RED-A1 (bis(2-methoxyethoxy)aluminum(III) sodium hydride) (2.67 mL, 8.88 mmol) in toluene at 5-7 °C under nitrogen and the mixture was stirred for 1 h in the cold. Thereupon, the mixture was quenched with sodium bicarbonate solution (ca. 40 mL) and stirred for 30 min. The organic phase was dried over MgS0 ₄ , filtered and evaporated to dryness to give the product as a yellowish oil. (Yield: 4.55 g, 96 %).

Step 8: tert-butyl (4R)-2-cyano-4-(2,3,5-trifluorophenyl)pyrrolidine-l-carboxyl ate

To a stirred solution of {AR)-tert-buty\ 2-methoxy-4-(2,3,6-trifluorophenyl)pyrrolidine-l- carboxylate (4.33 g, 11.76 mmol) in dry dichloromethane (90 mL) was added trimethylsilanecarbonitrile (3.15 mL, 23.52 mmol) followed by addition of boron trifluoride diethyl etherate (3.28 mL, 25.9 mmol) at -70 °C. The mixture was stirred for 4 h in the cold, quenched with sodium bicarbonate solution, and then allowed to warm up with stirring to room temperature. The organic phase was dried over MgSC , filtered and evaporated to dryness under vacuum to give the titled compound as a yellowish oil. (Yield: 4.41 g, 98 %).

Step 9: tert-butyl (4R)-2-carbamoyl-4-(2,3,6-trifluorophenyl)pyrrolidine-l-carb oxylate

To a stirred solution of {AR)-tert-buty\ 2-cyano-4-(2,3,6-trifluorophenyl)pyrrolidine-l- carboxylate (4.4 g, 11.46 mmol) in a mixture of acetone (54 mL) and water (18 mL) was added urea hydrogen peroxide complex (5.39 g, 57.3 mmol) followed by potassium carbonate (0.317 g, 2.292 mmol) and the reaction was stirred at room temperature for 16 h. Acetone was then partially removed under vacuum until oil separation. The mixture was diluted with water and petroleum ether, aged with stirring for 1 h at 5-7 °C (crystallization occurred). The solid was collected, washed with water, petroleum ether and dried to give {AR)-tert-buty\ 2-carbamoyl-4- (2,3, 6-trifluorophenyl)pyrrolidine-l-carboxy late. Yield: 3.46 g, 88 %.

Step 10: (4R -l-( tert-butoxycarbonyl)-4-( 2, 3, 6-tri luorophenyl)pyrrolidine-2-carboxylic acid

A stirred suspension of {AR)-tert-buty\ 2-carbamoyl-4-(2,3,6-trifluorophenyl)pyrrolidine-l- carboxylate (3.36 g, 9.76 mmol) in 2 M HC1 (73 mL, 146 mmol) was refluxed for 3 h to give a clear solution with minimum amount of dark insoluble material. After being cooled to room temperature the solid was filtered off and the filtrate was concentrated under vacuum. The residue was dissolved in water (ca. 50 mL), the pH was adjusted to 7 by addition of 1 M NaOH (19.52 mL, 19.52 mmol). The solution was then concentrated to approx. 50 mL and methanol (55 mL) was added followed by addition of di-ie/t-butyl dicarbonate (2.343 g, 10.73 mmol) and the mixture was stirred for 45 min. Methanol was then removed under vacuum, the residue was diluted with water (25 mL) and washed with petroleum ether. The aqueous phase was acidified to pH = 1-2 by addition of 2 M HC1, and then extracted with DCM (50 ml). The organic phase was dried over MgSC , filtered and evaporated to dryness to give (4 ?)-l-(ie/t-butoxycarbonyl)- 4-(2,3,6-trifluorophenyl)pyrrolidine-2-carboxylic acid as a light beige powder. Yield: 2.8 g, 83 %.

Step 11-14: ( ?)-l-methyl-6-(2,3,6-trifluorophenyl)-2,5,6,7-tetrahydro-3H- pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 122 (Steps 6-9) from {AR)-\-{tert- butoxycarbonyl)-4-(2,3,6-trifluorophenyl)pyrrolidine-2-carbo xylic acid and isolated as an off- white powder.

Ή NMR (DMSO-iM): 11.72 (1 Η, br s), 7.47 (1 Η, qd, J=9.4, 5.0 Hz), 7.17 (1 H, tdd, J=9.6, 9.6, 3.7, 1.9 Hz), 4.43 (1 H, quin, J=8.7 Hz), 4.14 (1 H, dd, J=11.3, 9.2 Hz), 3.73 (1 H, dd, J=11.5, 8.1 Hz), 3.24 (1 H, dd, J=15.6, 9.2 Hz), 2.86 (1 H, dd, J=15.4, 8.4 Hz), 1.97 (3 H, s).

1 ³ C NMR (DMSO- 6): 156.9, 156.9, 156.9, 156.9, 155.3, 155.3, 155.3, 155.3, 155, 149.1, 149, 149, 148.9, 147.5, 147.5, 147.4, 147.4, 147.3, 147.3, 145.9, 145.9, 145.8, 145.8, 127.6, 118.9, 118.8, 118.8, 118.7, 116.5, 116.4, 116.3, 116.3, 115.2, 112, 112, 111.9, 111.9, 111.8, 111.8, 111.8, 111.7, 48.4, 35.7, 28.6, 9.3. Example 130: ( ?)-6-(5-bromo-2-fluorophenyl)-l-methyl-2,5,6,7-tetrahydro-3H -pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 129 from 5-bromo-2- fluorobenzaldehyde and isolated as an off-white solid.

Ή NMR (DMSO-iM): 11.70 (1 H, br s), 7.58 (1 H, dd, J=6.6, 2.5 Hz), 7.53 (1 H, ddd, J=8.7, 4.5, 2.5 Hz), 7.23 (1 H, dd, J=10.3, 8.7 Hz), 4.20 (1 H, quin, J=8.1 Hz), 4.11 (1 H, dd, J=10.9, 8.2 Hz), 3.71 (1 H, dd, J=11.3, 7.9 Hz), 3.18 (1 H, dd, J=15.2, 8.1 Hz), 2.85 (1 H, ddd, J=15.2, 8.4, 1.1 Hz), 1.98 (3 H, s).

¹³ C NMR (DMSO-iM): 160.3, 158.7, 155.1, 131.8, 131.8, 131.4, 131.4, 130.6, 130.5, 127.6, 118, 117.9, 116.5, 116.4, 115.4, 49, 40.5, 29, 9.3. Example 131: ( ?)-6-(2,6-difluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2- c]imidazole-3-thione

Compound was prepared in an analogous manner to Example 129 from 2,6- difluorobenzaldehyde and isolated as an off-white solid.

Ή NMR (DMSO-iM): 11.72 (1 Η, br s), 7.40 (1 Η, tt, J=8.4, 6.6 Hz), 7.13 (2 H, m), 4.41 (1 H, quin, J=8.8 Hz), 4.12 (1 H, m), 3.70 (1 H, dd, J=11.4, 8.4 Hz), 3.21 (1 H, dd, J=15.2, 9.2 Hz), 2.84 (1 H, dd, J=15.4, 8.7 Hz), 1.97 (3 H, s).

¹³ C NMR (DMSO- 6): 161.6, 161.6, 160, 159.9, 155, 129.8, 129.7, 129.7, 127.8, 116.6, 116.5, 116.4, 115.2, 112.3, 112.2, 112.1, 112.1, 48.6, 35.4, 28.8, 9.3.

(5)-6-(5-chloro-2-fluorophenyl)- l-methyl-2,5,6,7-tetrahydro-3H-pyrrolo[l,2-

Compound was prepared in an analogous manner to Example 129 from 5-chloro-2- fluorobenzaldehyde using 4-(( ?)-hydroxy((15,25,45,5 ?)-5-vinylquinuclidin-2- yl)methyl)quinolin-6-ol as catalyst (CAS # 524-63-0) and isolated as a beige solid.

Ή NMR (DMSO-iM): 11.70 (1 H, br s), 7.46 (1 H, dd, J=6.5, 2.7 Hz), 7.40 (1 H, ddd, J=8.8, 4.4, 2.6 Hz), 7.29 (1 H, dd, J=10.1, 8.8 Hz), 4.20 (1 H, quin, J=8.1 Hz), 4.11 (1 H, dd, J=10.8, 8.1 Hz), 3.72 (1 H, dd, J=11.3, 7.9 Hz), 3.18 (1 H, dd, J=15.1, 8.1 Hz), 2.85 (1 H, ddd, J=15.2, 8.3, 1.2 Hz), 1.98 (3 H, s).

¹³ C NMR (DMSO-iM): 159.8, 158.2, 155.1, 130.2, 130.1, 128.9, 128.8, 128.5, 128.5, 127.6, 117.6, 117.4, 115.5, 49.1, 49.1, 40.5, 29, 9.3.

G. Dopamine-P-Hydroxylase Inhibition Assays

The ability of a compound to inhibit ϋβΗ activity may be assessed using the following cell assay. For the purposes of the present invention, a compound is considered to be a "ϋβΗ inhibitor" if it exhibits activity in "% of control" of < 20% at 10 μιη in this cell assay. Preferred compounds of the present invention (including most of the specific Examples above) exhibit activity in "% of control" of < 50% at 1.0 μιη in this cell assay. More preferred compounds of the present invention exhibit activity in "% of control" of < 20% at 1.0 μιη in this cell assay. Especially preferred compounds of the present invention exhibit activity in "% of control" of < 50% at 100 nm in this assay.

SK-N-SH cells (ATCC HTB-11), obtained from LGC Standards (Teddington, UK) were cultured in Eagle's minimum essential medium supplemented with 25 mM Hepes, 100 U/mL penicillin G, 0.25 μg/mL amphotericin B, 100 μg/mL streptomycin and 10% Gibco ^® fetal bovine serum. Cells were grown in T162 cm flasks (Corning, NY) in a humidified atmosphere of 5% C0 ₂ -95% air at 37 °C. Fetal bovine serum was removed from cells for 4 h prior to collection.

For the preparation of cellular homogenates, media was removed and cell monolayers were washed with 50 mM Tris-HCl pH 7.4. Cells were subsequently scrapped off the flasks and were resuspended in 50 mM Tris pH 7.4. Cell suspensions were homogenized with SilentCrusher M (Heidolph) for a short stroke and resultant homogenates were aliquoted and stored frozen at - 80 °C.

Total protein was quantified in cellular homogenates with BioRad Protein Assay (BioRad) using a standard curve of BSA (50-250 μg/mL). ϋβΗ activity was measured by a modification of the method of Nagatsu and Udenfriend (Nagatsu, T. and S. Udenfriend: "Photometric assay of dopamine-hydroxylase activity in human blood." Clin. Chem. 18(9): 980-3, 1972) which is based on the enzymatic hydroxy lation of tyramine into octopamine. The octopamine formed is subsequently oxidized to p- hydroxybenzaldehyde and measured by spectrophotometry. In brief, reaction mixture (total volume 500 μΐ) contained: cellular homogenate (75 μg total protein) sodium acetate pH 5.0 (200 mM), NEM (30 mM), CuS0 ₄ (5 μΜ), catalase aqueous solution (0.5 mg/mL), pargyline-HCl (1 mM), sodium fumarate (10 mM), ascorbic acid (10 mM), inhibitor or vehicle and tyramine (25 mM). After a 10 min pre-incubation period at 37 °C, the reaction was initiated by the addition of tyramine. Reaction was carried out for 45 min at 37 °C before termination with 50 μΐ PCA (2 M). Samples were centrifuged for 3 min at 16100 g and supernatants were subjected to solid phase extraction. Solid phase extraction was performed using either SPE cartridges ISOLUTE SCX-3 (100 mg, 1 mL) or SPE 2 mL fixed 96 well plates ISOLUTE SCX-3 (lOOmg) previously equilibrated with MilliQ water. Columns/plates were centrifuged at 150 g for 2 min. Eluate was discarded and matrix was washed with 1 mL of MilliQ water after which octopamine was eluted with 2x 0.25 mL ammonium hydroxide (4 M). The oxidation of octopamine to p- hydroxybenzaldehyde was carried out for 6 min with 100 μΐ sodium periodate (2%) and was stopped with 100 μΐ sodium metabisulfite (10%). Absorbance was measured at 330 nm on a Spectramax microplate reader (Molecular Devices, Sunnyvale, CA). All enzymatic reactions were performed in duplicate. Results are reported in the table below as activity in % of control at the inhibitor concentration tested.

Furthermore, the ability of a compound to inhibit ϋβΗ activity may be assessed in human plasma using the following assay. For the purposes of the present invention, a compound is considered to be a "ϋβΗ inhibitor" if it exhibits activity in "% of control" of < 20% at 10 μιη in this assay. Preferred compounds of the present invention (including most of the specific Examples above) exhibit activity in "% of control" of < 50% at 1.0 μιη in this cell assay. More preferred compounds of the present invention exhibit activity in "% of control" of < 20% at 1.0 μηι in this cell assay. Especially preferred compounds of the present invention exhibit activity in "% of control" of < 50% at 100 nm in this assay. Dopamine beta hydroxylase activity in human plasma was measured by the method previously developed (Nagatsu, T. and Udenfriend, S. Photometric assay of dopamine-β- hydroxylase activity in human blood. Clin. Chem. 18(9) 980-983, 1972) with minor modifications. Catalase, N-ethylmaleimide, tyramine, disodium fumarate, pargyline, sodium acetate, ascorbic acid, copper sulfate and octopamine were obtained from Sigma Chemical Co., St. Louis, Mo. 63178. Human plasma samples were obtained from healthy donors (Instituto Portugues do Sangue Transplantagao, Centra Sangue Transplantagao, Porto, Portugal). From date of collection, plasma was stored at -80 °C until use. Test compounds were initially prepared in dimethyl sulfoxide at a concentration of 10 mM and diluted in dimethyl sulfoxide to the required concentrations. Test compounds were further diluted in ultrapure water to a concentration 20-fold to that of the final concentration to be tested. Final concentrations of test compounds were 10, 100 and 1000 nM. The various reagents used to make up the incubation buffer were premixed and consisted of the following components: sodium acetate buffer (1 M, pH 5.0, 18 ml), sodium fumarate (0.2 M, 4.5 ml), ascorbic acid (0.2 M, 4.5 ml, freshly prepared), pargyline (20 mM, freshly prepared, 4.5 ml), N-ethylmaleimide (0.2 M, 4.5 ml), catalase (10 000 U/ml, 9 ml), copper sulfate (20 μΜ, 4.5 ml) and 4.5 ultrapure water. The standard incubation mixture (total volume, 950 μΐ) contained: 50 μΐ _^ of compound or vehicle (dimethyl sulfoxide 2%); 700 μΐ _^ of incubation buffer; 125 μΐ of plasma (or saline for blank reaction or standard curve); 75 μΐ of saline. The reaction mixture was placed in water bath, shaking at 37°C and pre- incubated for 10 minutes. Tyramine (0.5 M) was added and incubation proceeded for 45 minutes. The reaction contents were exposed to air. A sample of enzyme preparation (with 125 μΐ of plasma) that had been added perchloric acid 2 M at the end of the pre-incubation period was used as blank. A blank for each of the tested compounds was used. For octopamine standard curve, perchloric acid 2 M was replaced by increasing concentrations of octopamine prepared in perchloric acid 2 M (0.5, 1, 2.5, 5, 7.5, 10, 15, 20 μg/ml, final concentration). The incubation was stopped by adding 200 μΐ of 2 M molar perchloric acid, and the mixture was centrifuged at 9000 g for 5 min. The supernatant fluid (800 μί) was transferred to a column (SPE cartridge ISOLUTE SCX-3, 100 mg) and centrifuged at 150 g for 2 min. The column was washed two more times with 0.5 ml of ultrapure water by centrifuging at 150 g for 2 min. The adsorbed octopamine was eluted twice with 0.3 ml of 4 M ammonium hydroxide by centrifuging at 150 g for 2 min. Octopamine in the eluate was then converted to p-hydroxybenzaldehyde by adding 200μ1 of sodium periodate (2%) and incubating for 6 min. Excess periodate was than reduced by adding 200 μΐ of sodium metabisulfite (10%). Absorbance was measured at 330 mm in a 96-well plate by use of a SpectraMAX plus 384 (Molecular Devices) with software SOFTmax® PRO Software 5.3 spectrophotometer. Absorbance was linear with octopamine concentration from 0.5 to 20 μg/ml. Dopamine beta hydroxylase activity is determined as nmol of octopamine formed/ml of plasma/hour and effect of compounds is presented as % control.

Results are reported in the table below (inside brackets) as activity in % of control at the inhibitor concentration tested. H. MDCK Permeability Screening Assay

Madin-Darby canine kidney (MDCK) is a common cell line to assess membrane permeability of compounds. In this experiment, a value of -6 Log(cm/s) is indicative of a compound which is poorly permeable (e.g. Atenolol LogP _app = -6.2 Log(cm/s)) whilst a value of -4 Log(cm/s) is indicative of a compound which is highly permeable (e.g. Propranolol LogP _app = -4.2 Log(cm/s)). Preferred compounds of the present invention (including some of the specific Examples above (other Examples have not been tested)) exhibit a LogP _app higher than -6 Log(cm/s) in this assay. More preferred compounds of the present invention exhibit a P _app higher than -5 Log(cm/s) in this assay. Especially preferred compounds of the present invention exhibit a LogP _app higher than -4.5 Log(cm/s) in this assay.

MDCK-II cells (canine) were grown in MEM supplemented with 100 U/mL penicillin G,

0.25 μg/mL amphotericin B, 100 μg/mL streptomycin, 10% fetal bovine serum and 25 nM Hepes and maintained in a humified atmosphere of 5% C0 ₂ -95% air at 37 °C for 4 to 5 days. Transport experiments are performed in collagen treated 0.4 μιη polycarbonate filter support (12 mm ID, transwell, Co star-Corning) with compounds being applied from the apical (AP) cell border. The upper and lower chambers contained 400 and 1000 μΙ_, of Hank's Balance Salt Solution (HBSS), respectively. On the day of the experiments, cells were washed with HBSS, pH 7.4 and after a 5 min. pre-incubation period under gentle agitation, experiments were started by the addition of test compounds. Compounds are diluted in HBSS in order to have a final concentration of 50 μΜ with less than 1% DMSO. After 30 min. incubation, 250 μΐ _^ of medium was taken from the lower side to determine the optical transport. Samples were mixed with equal volume of acetonitrile with 0.1% formic acid and injected directly onto the LC-MS column. Apparent permeability coefficients (P _apP ) were calculated using the following equation:

V dC

P ^{app ~} AC ₀ ^{~ X ~} dt

Where V is the volume of the solution in the receiving compartment, A is the membrane surface area, Co is the initial concentration and dC/dt is the change in the drug concentration in the receiver over time. (Balimane, P. V.; Chong, S and Morrison, R. A.: J. Pharmacol. Toxicol. Methods, 44(1), 301-312, 2000). Results are reported as LogP _app in Log(cm/s).

I. Evaluation of Pharmacokinetic Profile

Adult male Wistar rats were kept under controlled environmental conditions (12 h light/dark cycle, room temperature 22+1 °C and humidity 50+5 %, food and tap water ad libitum). On the day before the experiment, the animals were fasted. In experiments designed to evaluate the pharmacokinetic profile of the compound of Examples 54, 61, 73, 74, 86 and 113, rats (n=4 per group) were administered orally (p.o.) with compounds (10 mg/kg/4ml; vehicle: 40% kleptose) and plasma and brain samples were collected from anaesthetized animals at 0.5, 1, 2, 4, 8, 15 and 24 h post-dosing. Animals were anaesthetized by intraperitoneal administration of sodium pentobarbital (60 mg/kg). Blood was collected from cardiac punction into heparinised tubes and kept on ice until centrifugation at 1,500 g for 15 min at 4°C. Plasma and brain samples were stored at less than -20°C until analysis.

After thawing, 200 μΐ of acetonitrile with 0.1% formic acid was added to 100 μΐ _^ of plasma. The samples were vortexed and centrifuged for 10 min at 10 000 g. Supernatant was filtered and injected into a mass spectrometer.

After thawing and weighing, water was added to the brain to give a tissue concentration of 0.1 mg/ml. The samples were then homogenized using a Heidolph DIAX 900 mixer and transferred to plastic tubes. Following centrifugation at 10 000 g for 20 min, supernatant was taken and treated as described for plasma.

J. ϋβΗ activity in rat adrenal gland homogenates

Dopamine beta hydroxylase activity in rat adrenal gland homogenates was measured by the method previously developed (Nagatsu, T. and Udenfriend, S. Photometric assay of dopamine-P-hydroxylase activity in human blood. Clin. Chem. 18(9) 980-983, 1972) with minor modifications. Catalase, N-ethylmaleimide, tyramine, disodium fumarate, pargyline, sodium acetate, ascorbic acid, copper sulfate and octopamine were obtained from Sigma Chemical Co., St. Louis, Mo. 63178. Test compounds were prepared in kleptose 40 % at a concentration of 0.75, 2.5 or 7.5 mg/mL to be administered at a dose of 10 mg/kg. Compounds and vehicle (kleptose 40%) were administered to wistar rats and adrenals were collected 0.5 h, 1 h, 2 h, 4 h, 8 h, 15 h and 24 h after administration. Samples were constituted by the right and left adrenals of each animal. Adrenals were stored in 200 μΐ _^ of 50 mM Tris pH 7.4 at -30 °C, from date of collection. The samples were homogenized and homogenates were then quantified for protein. Protein concentration was adjusted to 1.6 mg/ml. The various reagents used to make up the incubation buffer were premixed and consisted of the following components: sodium acetate buffer (1 M, pH 5.0, 6.0 mL), sodium fumarate (0.2 M, 1.5 mL), ascorbic acid (0.2 M, 1.5 mL, freshly prepared), pargyline (20 mM, freshly prepared, 1.5 mL), N-ethylmaleimide (0.2 M, 1.5 mL), catalase (55 000 U/ml, 3 mL), copper sulfate (90 μΜ, 1.67 mL) and ultrapure water (1.33 mL). The standard incubation mixture (total volume, 500 μί) contained: 350 μΐ _^ of incubation buffer; 125 μΐ _^ of protein sample (or buffer for blank reaction or standard curve). The reaction mixture was placed in water bath with shaking at 37 °C and pre-incubated for 10 minutes. Tyramine (0.4 M, 25 μί) was added and incubation proceeded for 45 minutes. The reaction contents were exposed to air. A sample of enzyme preparation (with 125 μL· of protein sample) that had been added perchloric acid 2 M at the end of the pre-incubation period was used as blank. A blank for each of the tested compounds was used. For octopamine standard curve, perchloric acid 2 M was replaced by increasing concentrations of octopamine prepared in perchloric acid 2 M (0.5, 1, 2.5, 5, 7.5, 10 μg/mL, final concentration). The incubation was stopped by adding 50 μΐ _^ of 2 M molar perchloric acid, and the mixture was centrifuged at 16000 g for 3 min. The supernatant fluid (500 μί) was transferred to a column (SPE cartridge ISOLUTE SCX-3, 100 mg) and centrifuged at 150 g for 2 min. The column was washed two more times with 0.5 ml of ultrapure water by centrifuging at 150 g for 2 min. The adsorbed octopamine was eluted twice with 250 μL· oΐ 4 M ammonium hydroxide by centrifuging at 150 g for 2 min. Octopamine in the eluate was then converted to p-hydroxybenzaldehyde by adding 100 μΐ _^ of sodium periodate (2%) and incubating for 6 min. Excess periodate was than reduced by adding 100 μΐ of sodium metabisulfite (10%). Absorbance was measured at 330 mm in a 96 well plate by use of a SpectraMAX plus 384 (Molecular Devices) with software SOFTmax® PRO Software 5.3 spectrophotometer. Absorbance was linear with octopamine concentration from 0.5 to 10 μg/mL. Dopamine beta hydroxylase activity is determined as nmol of octopamine formed/mg of protein/hour and effect of compounds is presented as % of control.

K. Biological data

In vitro experiments:

Example ϋβΗ activity in ϋβΗ activity in ϋβΗ activity in MDCK Permeability

% of Ctrl % of Ctrl % of Ctrl LogPapp

(Ο.ΙμΜ) (ΙμΜ) (10μΜ) (Log(cm/s))

1 75.6 42.4 4 -4.2

2 54.9 0 -3.9

3 89.0 53.8 3.9

4 18.6

5 83.2 0.8

6 97.6 50.3 3.3

7 84.8 37.7 7.5 -4

8 14.5 2.2 -3.9

9 30.9 5.3 -3.6

10 54.9 2.7 0 -3.9

11 86.4 31.4 1.5

12 63.0 11.5 0 -4.1

13 7.2

14 13.1

15 50.1 9.3 -4.1

16 55.5

17 56.8 -4.1

18 57.0 6.4

19 33.4

20 44.8

21 17.5

22 27.4

23 5.9 0 -4

24 40.2 15.9 -4

25 46.1 6.7 -4

26 21.4 -4

27 20.8 -3.9

28 0.2 3.3

29 26.9

30 3.3 2.8 -3.9

31 15.8 -4.1

32 57.3 4.7 -4

33 11.8 1.0

34 12.3 0 -4.2

35 95.0 34.3 0

36 4.0 0

37 59.7 2.4 -4.1

38 3.3 0 -4.1 40.4 0.3

87.9

29.8 0

44.1 -4

43.6 0 -3.7

70.9 13.7

29.1

31.6

45.3

43.0

60.6 -4

89.3 36.6 6.8 -3.9

54.4 -4

27.3 -4

66.5 11.8 -4.6

44.3 8.2 -4.6

61.0 0.4 -4.1

41.7 7.8 -4.8

97.9 58.6 9.2 -4.2

106.5 59.8 -3.9

100.1 27.8 -3.6

60.2

52.2 8.4

43.1 9.8

13.9

39.9 7.2

17.9

51.1 7.9

36.1

5.1

14.6

35.7

48.5

35.0

41.7 5.1

21.9 1.8

18.1

17.4

23.0

10.9

13.0

56.7

59.4

90.0 20.0

84.0 33.1

96.9 41.9

0 0

25.3 0

numbers in brackets represent activity in % of control in human plasma assay In vivo experiments:

Mean concentration-time profile of the compound of Example 54 in plasma and brain after oral administration of 10 mg/kg, to Wistar rats is shown in Figure 1. Each point represents mean + SD of 4 rats.

Mean concentration-time profile of the compounds of Example 54, 61, 73, 74, 86 and

113 in plasma after oral administration of 10 mg/kg to Wistar rats is shown in Figure 2. Each point represents mean + SD of 4 rats.

Mean concentration-time profile of the compounds of Example 54, 61, 73, 74, 86 and 113 in brain after oral administration of 10 mg/kg to Wistar rats is shown in Figure 3. Each point represents mean + SD of 4 rats.

ϋβΗ activity in ADR after oral administration of 10 mg/kg of compounds of Example 54, 61, 73, 74, 86 and 113 is shown in Figure 4. Each point represents mean + SD of 4 rats.