The present invention relates to a compound of formula I,

wherein

R ¹ is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; n is 1, 2 or 3; m is 1, 2 or 3;

Ar is a five or six membered heteroaryl group, selected from

wherein

R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen or lower alkoxy; R is hydrogen or halogen;

-() _m - is -(CH ₂ ) _D or to pharmaceutically active acid addition salts thereof.

Now it has been found that the present compounds of formula I are modulators of γ- secretase, they may be useful for the treatment or prevention of a disease associated with the deposition of β-amyloid in the brain, in particular Alzheimer's disease, and other diseases such as cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, Dutch-type (HCHWA-D), multi-infarct dementia, dementia pugilistica and Down syndrome.

Alzheimer's disease (AD) is the most common cause of dementia in later life.

Pathologically, AD is characterized by the deposition of amyloid in extracellular plaques and intracellular neurofibrillary tangles in the brain. The amyloid plaques are mainly composed of amyloid peptides (Αβ peptides) which originate from the β-Amyloid Precursor Protein (APP) by a series of proteolytic cleavage steps. Several forms of APP have been identified of which the most abundant are proteins of 695, 751 and 770 amino acids length. They all arise from a single gene through differential splicing. The Αβ peptides are derived from the same domain of the APP.

Αβ peptides are produced from APP through the sequential action of two proteolytic enzymes termed β- and γ-secretase. β-Secretase cleaves first in the extracellular domain of APP just outside of the trans-membrane domain (TM) to produce a C-terminal fragment of APP (ΟΓΕβ) containing the TM- and cytoplasmatic domain. CTFβ is the substrate for γ-secretase which cleaves at several adjacent positions within the TM to produce the Αβ peptides and the cytoplasmic fragment. Various proteolytic cleavages mediated by γ-secretase result in Αβ peptides of different chain length, e.g. Αβ38, Αβ40 and Αβ42. The latter one is regarded to be the more pathogenic amyloid peptide because of its strong tendency to form neurotoxic aggregates.

The β-secretase is a typical aspartyl protease. The γ-secretase is a high molecular weight complex that consists of four essential subunits: Presenilin (PS, including PS1 and PS2), nicastrin, anterior pharynx defective 1 (APH-1), and presenilin enhancer 2 (PEN-2). The atomic structure of human γ-secretase at 3.4 A resolution has been published (X. Bai, C. Yan, G. Yang, P. Lu, D. Ma, L. Sun, R. Zhou, S. H. W. Scheres, Y. Shi, Nature 2015, 525, pages 212 - 217. The presenilins are bearing the catalytic site and represent a group of atypical aspartyl proteases which cleave their substrates within the TM of and which are themselves polytopic membrane proteins. The other essential components of γ-secretase , nicastrin and the products of the aphl and pen-2 genes are believed to be responsible for substrate recognition and recruitment. Proven substrates for γ-secretase are APP and the proteins of the Notch receptor family, however, γ- secretase has a loose substrate specificity and many further membrane proteins unrelated to APP and Notch have been reported to be cleaved by the γ-secretase in vitro.

The γ-secretase activity is absolutely required for the production of Αβ peptides. This has been shown both by genetic means, i.e., ablation of the presenilin genes and by low-molecular- weight inhibitory compounds. According to the amyloid cascade hypothesis for AD the production and deposition of Αβ is the ultimate cause for the disease. Therefore, it was believed that selective and potent inhibition of γ-secretase might be useful for the prevention and treatment of AD.

An alternative mode of treatment is the modulation of the γ-secretase activity which results in a selective reduction of the Αβ42 production. This will lead in an increase of shorter Αβ isoforms, such as Αβ38, Αβ37 or others, which have no or reduced capability for aggregation and plaque formation, and are not or less neurotoxic. Compounds which show this effect on modulating γ-secretase activity include certain non-steroidal anti-inflammatory drugs (NSAIDs) and related analogues (Weggen et al., Nature, 414 (2001) 212-16).

Thus, the compounds of this invention will be useful for the treatment or prevention of a disease associated with the deposition of β-amyloid in the brain, in particular Alzheimer's disease, and other diseases such as cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, Dutch-type (HCHWA-D), multi-infarct dementia, dementia pugilistica and Down syndrome.

Numerous documents describe the current knowledge on γ-secretase modulation, for example the following publications:

Morihara et al, J. Neurochem., 83 (2002) 1009-12

Jantzen et al, J.Neuroscience, 22 (2002) 226-54

Takahashi et al, J. Biol. Chem., 278 (2003) 18644-70

Beher et al, J. Biol. Chem. 279 (2004) 43419-26

Lleo et al, Nature Med. 10 (2004) 1065-6

Kukar et al, Nature Med. 11 (2005) 545-50

Perretto et al, J. Med. Chem. 48 (2005) 5705-20

Clarke et al, J. Biol. Chem. 281 (2006) 31279-89

Stock et al, Bioorg. Med. Chem. Lett. 16 (2006) 2219-2223

Narlawar et al, J. Med. Chem. 49 (2006) 7588-91

Ebke et al, J. Biol. Chem., 286 (2011) 37181-86 Oehlich, Gijsen et al, J. Med. Chem., 54 (2011), 669 - 698

Li et al., Biochemistry, 52, (2013), 3197 - 3216

Hall et al, Progress in Med. Chem., 53 (2014) 101-145

Bursavich et al, J. Med. Chem., 59 (2016) DOI: 10.1021/acs.jmedchem.5b01960

The following definitions for compounds of formula I are used:

As used herein, the term "lower alkyl" denotes a saturated straight- or branched-chain group containing from 1 to 7 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, n- butyl, i-butyl, 2-butyl, t-butyl and the like. Preferred alkyl groups are groups with 1 - 4 carbon atoms.

As used herein, the term "lower alkyl substituted by halogen" denotes an alkyl group as defined above, wherein at least one hydrogen atom is replaced by halogen, for example CF ₃ , CHF ₂ , CH ₂ F, CHFCF ₃ , CH ₂ CHF ₂ , CH ₂ CH ₂ F, CH ₂ C(CH ₃ ) ₂ CF ₃ , CH ₂ CF ₂ CF ₃ , CH(CF ₃ ) ₂ , CH ₂ CF ₃ , (CH ₂ ) ₂ CF ₃ , (CH ₂ ) ₃ CF ₃ , CH(CH ₃ )CF ₃ , CF ₂ CF ₃ , and the like. The preferred group is CF ₃ .

The term "lower alkoxy" denotes a lower alkyl group as defined above, which group is connected via an O atom.

The term "lower alkoxy substituted by halogen" denotes a lower alkoxy group as defined above, wherein at least one hydrogen atom is replaced by halogen.

The term "halogen" denotes chlorine, iodine, fluorine and bromine.

The term "pharmaceutically acceptable acid addition salts" embraces salts with inorganic and organic acids, such as hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methane- sulfonic acid, p-toluenesulfonic acid and the like.

Objects of the present invention are compounds of formula I, the use of such compounds for the preparation of medicaments for the treatment of Alzheimer' s disease, cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, Dutch-type (HCHWA-D), multi- infarct dementia, dementia pugilistica or Down syndrome, their manufacture and medicaments based on a compound of formula I in accordance with the invention.

Further objects of the present invention are all forms of optically pure enantiomers, racemates or diastereometric mixtures for compounds of formula I.

One object of the present invention is a compound of formula 1-1, wherein

R ¹ is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; n is 1, 2 or 3; m is 1, 2 or 3;

R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen or lower alkoxy; or a pharmaceutically active acid addition salts thereof, for example the following compounds

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(2-chloro-4-pyridyl)-3-azabicyclo[3.2.1]octa n-8-yl]-4-(3,4-difluorophenyl)-6,7- dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-5,6-dihydroimidazo[l,2-b][l,2,4 ]triazol-2-amine

4-[4-(trifluoromethyl)phenyl]-N-[(lR,5S,8S)-3-[2-(trifluorom ethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

4-[4-(trifluoromethyl)phenyl]-N-[(lR,5S,8S)-3-[2-(trifluorom ethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine

4-(3-fluoro-4-methyl-phenyl)-N-[(lR,5S,8S)-3-[2-(trifluor omethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl) -3-azabicyclo[3.2.1]octan-8-yl]-

6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine 4-(3,4-dif uorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]- 3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo [3.2.1]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4 3-fluorophenyl)-N-[(lR,5S,8S)-3-[2 trifluoromethyl)-4-pyridyl]-3-azabicyclo[3.2^]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

4 4-fluorophenyl)-N-[(lR,5S,8S)-3-[2 trif uoromethyl)-4-pyridyl]-3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-a zabicyclo[3.2.1]octan-8-yl]-6,7- dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,5-dif uorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]- 3- azabicyclo[3.2 ]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin- 2-amine

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl)- 3-azabicyclo[3.2.1]octan-8-yl]-6,7- dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,5-dif uorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-azabicyc lo[3.2.1]octan-8-yl]- 6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine or

4^4-methoxyphenyl)-N-[(lR,5S,8S)-3-[2^trifluoromethyl)-4-pyr idyl]-3-azabicyclo[3.2.1]octan- 8-yl]-6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine.

One further object of the present invention is a compound of formula 1-2,

wherein

R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; n is 1, 2 or 3; m is 1, 2 or 3; R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen or lower alkoxy; R is hydrogen or halogen; or a pharmaceutically active acid addition salts thereof, for example the following compounds 4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-8- yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-8- yl]-5,6-dihydroimidazo[ 1,2-b] [ 1 ,2,4]triazol-2-amine

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-5,6,7,8-tetrahydro-[ 1 ,2,4]triazolo[ 1 ,5-a] [ 1 ,3]diazepin-2-amine

4-(3-fluoro-4-methyl-phenyl)-N-[(lR,5S,8S)-3-(6-methylpyr imidin-4-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-5,6-dihydroimidazo[l,2-b][l,2,4]tri azol-2-amine

N-[(lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-(3-fluoro-4-methyl- phenyl)-6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidi n-4-yl)-3-azabicyclo[3.2.1]octan-8- yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-(3,4- difluorophenyl)-6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(5-fluoro-6-methyl -pyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-8- yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin-2 -amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4 -yl)-3-azabicyclo[3.2.1]octan-8- yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin-2 -amine

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3-azabicyclo[3. 2.1]octan-8-yl]-4-(2,3,4- trif uorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

4 3-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-a zabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H-[ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4 4-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-a zabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H-[ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4^4-iluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)- 3-azabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H-[ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

4 3,5-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl) -3-azabicyclo[3.2.1]octan-8- yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin^^

fluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azab icyclo[3 .1]octan-8-yl]-4-(3- fluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3-f uorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3-azab icyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine or

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(2,3,4- trif uorophenyl)-5,6-dihydroimidazo[ 1 ,2-b] [ 1 ,2,4]triazol-2-amine.

One object of the present invention is a com ound of formula 1-3,

wherein

R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; n is 1, 2 or 3; m is 1, 2 or 3; R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen or lower alkoxy; or a pharmaceutically active acid addition salts thereof, for example the following compounds N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3,4- difluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4 -yl)-3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyridazin-4- yl)-3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3,4- difluorophenyl)-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l, 3]diazepin-2-amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazi n-4-yl)-3-azabicyclo[3.2.1]octan-8- yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin-2 -amine

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyridazin -4-yl)-3-azabicyclo[3.2.1]octan-8- yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin-2 -amine

N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2 .1]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3-azabicyclo[3. 2.1]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[ 1 ,2,4]triazolo[ 1 ,5-a]pyrimidin-2-amine

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl) -3-azabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine or

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl) -3-azabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5-a]pyrimidin-2-amine.

One object of the present invention is a com ound of formula 1-4,

wherein R ¹ is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; n is 1, 2 or 3; m is 1, 2 or 3; or a pharmaceutically active acid addition salts thereof, for example the following compounds

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(3-methyl-l,2,4-oxadi azol-5-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine or 4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(3-methyl-l,2,4-oxadi azol-5-yl)-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine.

Further objects of the present invention are compounds of formulas

wherein

R ¹ is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, lower alkoxy or lower alkoxy substituted by halogen;

R ¹ may be the same or different, if n = 2 or 3; is 1, 2 or 3; is a five or six membered heteroaryl group, selected from

wherein

R is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen or lower alkoxy; R is hydrogen or halogen; or pharmaceutically active acid addition salts thereof.

The present compounds of formula I and their pharmaceutically acceptable salts can prepared by methods known in the art, for example, by processes described below, which processes comprise

a) reacting a compound of formula 9

with a compound of formula 10

to a compound of formula I

wherein the substituents have the meaning as described above, and,

if desired, converting the compounds obtained into pharmaceutically acceptable acid addition salts; more detail, compounds of formula I and their intermediates may be prepared by schemes - 4 and by the description of 50 specific examples.

General synthesis schemes

General Synthesis of derivatives of type la with m = 1

Scheme 1

9

The preparation of derivatives of general formula la with (m =1), where made according to the scheme 1. The synthesis of target compounds commenced by the nucleophilic addition of a commercially available substituted anilines 2 onto the diphenyl cyanocarbonimidate 3 leading to the intermediates 4 in a good yield. Upon N-alkylation with an electrophile [2- (2- bromoethoxy)tetrahydropyran] containing a protected alcohol moiety the compounds 5 were obtained. Upon reaction with hydrazine the corresponding triazoles 6 were obtained.

Deprotection of the alcohol protected by tetrahydropyran (THP) group under standard acidic conditions afforded 7 in nearly quantitative yield, the alcohol precursor for the Mitsunobu reaction forming 8. Finally, a Sandmeyer reaction led to the Versailles intermediates

bromotriazole 9, which can easily undergo a Buchwald type reaction with different amines of type 10 affording final products of formula la. General Synthesis of derivatives of type lb with m

Scheme 2

The preparation of derivatives of general formula lb with (m =2), where made according to the scheme 2. The synthesis of target compounds commenced by the nucleophilic addition of a commercially available substituted anilines 2 onto the diphenyl cyanocarbonimidate 3 leading to the intermediates 4 in a good yield. Upon N-alkylation with an electrophile [2-(3- bromopropoxy)tetrahydropyran] containing a protected alcohol moiety the compounds 11 were obtained. Upon reaction with hydrazine the corresponding triazoles 12 were obtained.

Deprotection of the alcohol protected by tetrahydropyran (THP) group under standard acidic conditions afforded 13 in nearly quantitative yield, the alcohol precursor for the Mitsunobu reaction forming 14. Finally, a Sandmeyer reaction led to the Versailles intermediates bromotriazole 15, which can easily undergo a Buchwald type reaction with different amines of type 10 affording final products of formula lb. General Synthesis of derivatives of type Ic with

Scheme 3

The preparation of derivatives of general formula Ic with (m =3), where made according to the scheme 3. The synthesis of target compounds commenced by the nucleophilic addition of a commercially available substituted anilines 2 onto the diphenyl cyanocarbonimidate 3 leading to the intermediates 4 in a good yield. Upon N-alkylation with an electrophile [2-(4- bromobutoxy)tetrahydropyran] containing a protected alcohol moiety the compounds 16 were obtained. Upon reaction with hydrazine the corresponding triazoles 17 were obtained.

Deprotection of the alcohol protected by tetrahydropyran (THP) group under standard acidic conditions afforded 18 in nearly quantitative yield, the alcohol precursor for the Mitsunobu reaction forming 19. Finally, a Sandmeyer reaction led to the Versailles intermediates bromotriazole 20, which can easily undergo a Buchwald type reaction with different amines of type 10 affording final products of formula Ic. General synthesis of derivatives 10

Scheme 4

21 or Pd coupling _{22 10}

Compounds of formula 10 used in schemes 1-3 can be prepared according to the scheme 4. can be synthesized starting from tert-butyl N-[(lS,5R,8S)-3-azabicyclo[3.2. l]octan-8-yl]carbamate 21 (CAS 847862-26-4 ). The coupling of 21 with heterocyclic halides of general formula Ar-X can be accomplished under thermal conditions in a solvent such as ethanol or NMP in the presence of a base such as Et ₃ N or by using displacement reactions under catalytic conditions (like e.g. palladium(O) or copper(II) catalysis) to provide compounds of formula 22. After deprotection with acid e.g. trifluoro acetic acid compounds of formula 10 were obtained.

The heterocycles halides are either commercial available, known in the literature so they can be prepared by methods known in the art or alternatively could be prepared as described in the specification.

The compounds were investigated in accordance with the test given hereinafter. Description of γ-secretase assay

Cellular γ-secretase assay

Human neuroglioma H4 cells overexpressing human APP695 with the Swedish double mutation (K595N/M596L) were plated at 30,000 cells/well/ 100 μΐ in 96-well plates in EVIDM media containing 10% FCS, 0.2 mg/1 Hygromycin B and incubated at 37°C, 5% C0 ₂ .

3-4 hr post plating, compounds are a diluted in media and 50 μΐ is added as 1.5-fold concentrate to achieve the final concentration. Compound incubation is performed for 24 hr. Final doses typically range from 4 μΜ down to 0.0013 μΜ in half-log steps resulting in a eight point dose response curve.

Appropriate controls using vehicle only and reference compound were applied to this assay. The final concentration of Me ₂ SO was 0.4%.

After incubation at 37°C, 5% C0 ₂ , the supernatant was subjected to quantification of secreted Αβ42 by the means of an AlphaLisa assay kit (Human Amyloid beta 1-42 Kit: Cat# AL203C, Perkin Elmer). 20 μΐ of the cell culture supernatant was transferred to an assay plate. Then 10 μΐ of a mixture of the AlphaLisa coupled capture antibody and the biotinylated detection antibody was added and incubated for 3 hours at room temperature while softly shaking the assay plate. After a further addition of 20 μΐ of the Donor beads the assay plate was incubated for 30 min at room temperature and constant shaking without exposure to direct light. The assay plate was then read on a Paradigm AlphaLisa Reader using the build-in program with excitation at 680 nm and emission at 570 nm.

The measured signals were then used to calculate IC ₅₀ values for inhibition of Αβ42 secretion by nonlinear regression fit analysis using XLfit 5.3 software (IDBS).

The table below shows the data for all compounds for the inhibition of Αβ42 secretion

(nM):

Example No. EC50 Αβ42 Example No. EC50 Αβ42

(uM) (nM)

1 0.0158 26 0.0463

2 0.0059 27 0.0378

3 0.0264 28 0.0593

4 0.0892 29 0.0233

5 0.0356 30 0.0320

6 0.0214 31 0.0294

7 0.0302 32 0.0277

8 0.0117 33 0.0404

9 0.0192 34 0.0144

10 0.0312 35 0.0306

11 0.0278 36 0.0232

12 0.0268 37 0.0344

13 0.0114 38 0.0402

14 0.0155 39 0.0141

15 0.0306 40 0.0092

16 0.0172 41 0.0158

17 0.0580 42 0.0406

18 0.0264 43 0.0259 19 0.0139 44 0.0308

20 0.0231 45 0.0130

21 0.0147 46 0.0103

22 0.0348 47 0.0234

23 0.0233 48 0.0264

24 0.0804 49 0.0064

25 0.0234 50 0.0570

The compounds of formula I and the pharmaceutically acceptable salts of the compounds of formula I can be used as medicaments, e.g. in the form of pharmaceutical preparations. The pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions. The administration can, however, also be effected rectally, e.g. in the form of suppositories, parenterally, e.g. in the form of injection solutions. The administration can also be effected topically, e.g. transdermal administration, or in form of eye drops or ear drops.

The compounds of formula I can be processed with pharmaceutically inert, inorganic or organic carriers for the production of pharmaceutical preparations. Lactose, corn starch or derivatives thereof, talc, stearic acids or its salts and the like can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules. Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like. Depending on the nature of the active substance no carriers are, however, usually required in the case of soft gelatine capsules. Suitable carriers for the production of solutions and syrups are, for example, water, polyols, glycerol, vegetable oil and the like. Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like.

The pharmaceutical preparations can, moreover, contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.

Medicaments containing a compound of formula I or a pharmaceutically acceptable salt thereof and a therapeutically inert carrier are also an object of the present invention, as is a process for their production, which comprises bringing one or more compounds of formula I and/or pharmaceutically acceptable acid addition salts and, if desired, one or more other therapeutically valuable substances into a galenical administration form together with one or more therapeutically inert carriers.

In accordance with the invention compounds of formula I as well as their

pharmaceutically acceptable salts are useful in the control or prevention of illnesses based on the inhibition of Αβ42 secretion, such as of Alzheimer's disease.

The dosage can vary within wide limits and will, of course, have to be adjusted to the individual requirements in each particular case. In the case of oral administration the dosage for adults can vary from about 0.01 mg to about 1000 mg per day of a compound of general formula I or of the corresponding amount of a pharmaceutically acceptable salt thereof. The daily dosage may be administered as single dose or in divided doses and, in addition, the upper limit can also be exceeded when this is found to be indicated.

Tablet Formulation (Wet Granulation)

Item Ingredients mg/tablet

5 25 100 500

1. Compound of formula I 5 25 100 500

2. Lactose Anhydrous DTG 125 105 30 150

3. Sta-Rx 1500 6 6 6 30

4. Microcrystalline Cellulose 30 30 30 150

5. Magnesium Stearate 1 1 1 1

Total 167 167 167 831

Manufacturing Procedure

1. Mix items 1, 2, 3 and 4 and granulate with purified water.

2. Dry the granules at 50°C.

3. Pass the granules through suitable milling equipment.

4. Add item 5 and mix for three minutes; compress on a suitable press. Capsule Formulation

Item Ingredients mg/capsule

5 25 100 500

1. Compound of formula I 5 25 100 500

2. Hydrous Lactose 159 123 148 —

3. Corn Starch 25 35 40 70

4. Talc 10 15 10 25

5. Magnesium Stearate 1 2 2 5

Total 200 200 300 600 Manufacturing Procedure

1. Mix items 1, 2 and 3 in a suitable mixer for 30 minutes.

2. Add items 4 and 5 and mix for 3 minutes.

3. Fill into a suitable capsule.

Experimental Part The following examples are provided for illustration of the invention. They should not be considered as limiting the scope of the invention, but merely as being representative thereof.

General

Analytical methods

HPLC (method LCMS_fastgradient)

Column: Agilent Zorbax Eclipse Plus C18, Rapid Resolution HT, 2.1x30 mm, 1.8μιη,

Part.no. 959731-902

Solvent A: Water 0.01% Formic Acid; Solvent B: acetonitrile (MeCN)

Gradients:

Abbreviations

The following abbreviations were used in the experimental part:

THF = tetrahydrofurane; TBME = methyl-tert-butylether;

DMF = dimethylformamide;

TLC = thin layer chromatography;

RT = room temperature, 20-25°C.

Preparation of intermediates

Intermediates of type 9 (according to scheme 1)

Intermediate 9-1:

2-bromo-4-(3,4-difluorophenyl)-5,6-dihydroimidazo[l,2-b][l,2 ,4]triazole

Step 1: 3,4-Difluoroaniline (3.00 g, 23.20 mmol) and diphenyl cyanocarbonimidate (5.53 g, 23.20 mmol) were dissolved in 2-propanol (64.00 mL). The reaction mixture was stirred at RT overnight. The crude was evaporated in vacuo and purified by column chromatography

(Hept:EtOAc 100:0 to 50:50) to afford (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)

carbamimidate as a white solid (5.00 g, 79%). MS (ES+) m/z: 214.1 [M+H] ⁺ .

Step 2: A solution of 2-(2-bromoethoxy)tetrahydro-2H-pyran (5.74 g, 4.15 mL, 27.40 mmol), (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)carbamimidate (5.00 g, 18.30 mmol) and K ₂ CO ₃ (5.06 g, 36.60 mmol) in DMF (180 mL) was heated at 85°C overnight. An extra amount of 2-(2- bromoethoxy)tetrahydro-2H-pyran (5.74 g, 4.15 mL, 27.40 mmol) and K ₂ C0 ₃ (5.06 g, 36.60 mmol) were added and the reaction stirred at 100°C for a further 8 hours and then at 75°C overnight. The reaction mixture was cooled down to RT, poured onto a saturated aqueous solution of NH ₄ CI and the product extracted three times with EtOAc. The organic layers were combined, washed with water and then with brine, dried over sodium sulfate, filtered and evaporated in vacuo. The residue was then purified by column chromatography using

(Hept:EtOAc 100:0 to 70:30) to afford (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)-N-(2- ((tetrahydro-2H-pyran-2-yl)oxy)ethyl)carbamimidate as a yellow oil (1.75 g, 24%). MS (ES+) m/z: 402.2 [M+H] ⁺ . Step 3: To a solution of (Z)-Phenyl N'-cyano-N-(3,4-difluorophenyl)-N-(2-((tetrahydro-2H- pyran-2-yl)oxy)ethyl) carbamimidate (1.75 g, 4.36 mmol) in methanol (12 mL) was added hydrazine hydrate 25% in H ₂ 0 (873 mg, 864.00 μΐ, 4.36 mmol). The reaction mixture was stirred at 35°C for 1 hour and then evaporated in vacuo to give N3-(3,4-Difluorophenyl)-N3-(2- ((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-4H-l,2,4-triazole-3,5- diamine (1.79 g, 91%) which was used directly for the next step without further purification. (1.79 g, 91%). MS (ES+) m/z: 340.2 [M+H] ⁺ .

Step 4: The crude of N3-(3,4-difluorophenyl)-N3-(2-((tetrahydro-2H-pyran-2-yl)oxy )ethyl)-4H- l,2,4-triazole-3,5-diamine (1.79 g, 5.27 mmol) was dissolved in a mixture of aqueous HC1 2M (9 mL) an methanol (43 mL). The reaction mixture was stirred at RT for 1 hour and concentrated in vacuo. The residue was diluted with EtOAc and washed with an aqueous NaHC0 ₃ solution. The organic layer was dried Na ₂ S0 ₄ and the product purified by combiflash chromatography

(CH ₂ Cl ₂ :MeOH 100:0 to 90: 10) to afford 2-((5-Amino-4H-l,2,4-triazol-3-yl)(3,4- difluorophenyl)amino)ethanol as a white solid (0.39 g, 29%). MS (ES+) m/z: 256.2 [M+H] ⁺ .

Step 5: To a THF (4 mL) solution of 2-((5-Amino-4H-l,2,4-triazol-3-yl)(3,4-difluorophenyl) amino)ethanol (50.00 mg, 196 μιηοΐ) and triphenylphosphine (154 mg, 588 μιηοΐ) was added DEAD (70 mg, 64 μΐ, 392 μιηοΐ) the reaction was stirred at RT for 24 hours. The reaction was stirred for further 7 hours at 50°C and then one extra amount of triphenylphosphine (154 mg, 588 μιηοΐ), DEAD (70 mg, 64 μΐ, 392 μιηοΐ) and THF (4 mL) were added. The reaction mixture was left to stir at RT overnight. The mixture was diluted with EtOAc and washed three times with water and brine; the organic phase was dried over sodium sulfate, filtered and evaporated in vacuo. The crude was purified using combiflash chromatography (CH ₂ Cl ₂ :MeOH 100:0 to 90: 10) to afford 4-(3,4-difluorophenyl)-5,6-dihydro-4H-imidazo[l,2-b][l,2,4]t riazol-2-amine as a white solid (7.2 mg, 15%). MS (ES+) m/z: 238.1 [M+H] ⁺ .

Step 6: iert-Butyl nitrile (232 mg, 268 μΐ, 2.0 mmol) and cupric bromide (452 mg, 96 μΐ, 2.0 mmol) were combined in CH ₃ CN (40 mL) and stirred at 60°C before a solution of 4-(3,4- difluorophenyl)-5,6-dihydro-4H-imidazo[l,2-b][l,2,4]triazol- 2-amine (140 mg, 590 μιηοΐ) in CH ₃ CN (40 mL) was added drop wise. The reaction mixture was stirred at 75°C for 2 hours, concentrated in vacuo, diluted with 1M HC1 and extracted three times with EtOAc. The combined organic layer was dried over sodium sulfate, filtered and evaporated in vacuo. The crude was purified by combiflash chromatography (Hept:EtOAc 100:0 to 50:50) to afford 2- bromo-4-(3,4-difluorophenyl)-5,6-dihydro-4H-imidazo[l,2-b][l ,2,4]triazole (0.12 g, 69%) as off-white solid. MS (ES+) m/z: 301.0 and 303.0 [M+H] ⁺ . (Br isotopes).

Intermediate 9-2:

2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6-dihydroimidazo[l,2 -b][l,2,4]triazole

In analogy to the preparation of the intermediate 9-1, starting from 4-(trifluoromethyl)aniline was prepared 0.12 g of the intermediate 2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6-dihydro imidazo[l,2-b][l,2,4]triazole (9-2) as a white solid. MS (ES+) m/z: 333.0 and 335.0 [M+H] ⁺ . (Br isotopes)

Intermediate 9-3:

2-bromo-4-(2,3,4-trifluorophenyl)-5,6-dihydroimidazo[l,2-b][ l,2,4]triazole

In analogy to the preparation of the intermediate 9-1, starting from 2,3,4-trifluoroaniline was prepared 0.12 g of the intermediate 2-bromo-4-(2,3,4-trifluorophenyl)-5,6-dihydroimidazo[l,2- b][l,2,4]triazole (9-3) as a white solid. MS (ES+) m/z: 319.0 and 321.0 [M+H] ⁺ . (Br isotopes)

Intermediates of type 15

Intermediate 15-1:

2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazol o[l,5-a]pyrimidine

Step 1: 3,4-Difluoroaniline (3.00 g, 23.20 mmol) and diphenyl cyanocarbonimidate (5.53 g, 23.20 mmol) were dissolved in 2-propanol (64.00 mL). The reaction mixture was stirred at RT overnight. The crude was evaporated in vacuo and purified by column chromatography

(Hept:EtOAc 100:0 to 50:50) to afford (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)

carbamimidate as a white solid (5.00 g, 79%). MS (ES+) m/z: IM [M+H] ⁺ .

Step 2: A solution of (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)carbamimidate (17.69 g, 64.70 mmol), 2-(3-bromopropoxy)tetrahydro-2H-pyran (22.80 g, 17.10 mL, 97.10 mmol) and K ₂ CO ₃ (17.90 g, 129.00 mmol) in DMF (200 mL) was heated overnight at 85°C. The reaction mixture was concentrated in vacuo and the residue was purified by column chromatography

(Hept:EtOAc 90: 10 to 50:50) to give 3-cyano-l-(3,4-difluorophenyl)-2-phenyl-l-(3- tetrahydropyran-2-yloxypropyl)isourea as a white solid (26.90 g, 49%). MS (ES+) m/z: 416.2 [M+H] ⁺ .

Step 3: To a solution of of (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)-N-(3-((tetrahydro-2H- pyran-2-yl)oxy)propyl)carbamimidate (10.20 g, 24.60 mmol) in MeOH (70 mL) was added hydrazine hydrate 25% in water (4.92 g, 4.87 mL, 24.60 mmol). The reaction mixture was stirred at RT overnight, evaporated and purified by column chromatography (CH ₂ Cl ₂ :MeOH 99: 1 to 92.5:7.5) to afford N3-(3,4-difluorophenyl)-N3-(3-tetrahydropyran-2-yloxypropyl) -4H-l,2,4- triazole-3,5-diamine as a colourless foam (8.68 g, 78%). MS (ES+) m/z: 354.2 [M+H] ⁺ .

Step 4: To a solution of N3-(3,4-difluorophenyl)-N3-(3-((tetrahydro-2H-pyran-2-yl)oxy )propyl)- 4H-l,2,4-triazole-3,5-diamine (6.75 g, 19.10 mmol) in MeOH (150 mL) followed by addition of aqueous HC1 2M (30 mL). The reaction mixture was stirred at RT for 90 minutes and

concentrated in vacuo. The residue was diluted with EtOAc and washed with an aqueous NaHC0 ₃ solution. The organic layer was dried on Na ₂ S0 ₄ and the product purified by combiflash chromatography to afford 3-(N-(5-Amino-4H-l,2,4-triazol-3-yl)-3,4-difluoro- anilino)propan-l-ol as a white solid (5.14 g, 95%). MS (ES+) m/z: 270.1 [M+H] ⁺ . Step 5: To a solution of 3-((5-amino-4H-l,2,4-triazol-3-yl)(3,4-difluorophenyl)amino) propan-1- ol (4.55 g, 16.90 mmol) in DMF (90 mL) at -15/-20°C, was added triphenylphosphine (6.65 g, 25.30 mmol). The mixture was stirred at -15/-20°C for 15 minutes, then at -30°C, DEAD (4.55 g, 4.10 ml, 25.30 mmol) was added drop wise over of 20 minutes. The mixture was stirred at -30°C for 90 minutes. Water was added to the reaction mixture and then concentrated under vacuo, and the product extracted with EtOAc. The combined organic layers were washed once with brine, dried over sodium sulfate, filtered and evaporated in vacuo. The crude was purified using silica chromatography (CH ₂ Cl ₂ :MeOH 99: 1 to 96:4) to afford 4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidin-2-amine as a white solid (3.41 g, 80%). MS (ES+) m/z: 252.1 [M+H] ⁺ .

Step 6: To a black solution of iert-butyl nitrite (1.01 g, 1.17 mL, 8.86 mmol) and cupric bromide (1.98 g, 420 μΐ, 8.86 mmol) in CH ₃ CN (150 mL) at 60°C, 4-(3,4-difluorophenyl)-4,5,6,7- tetrahydro-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine (1.63 g, 5.90 mmol,) in 50 mL CH ₃ CN was added drop wise. After addition, the reaction mixture was heated to 75°C and stirred for 30 minutes. The reaction mixture was concentrated in vacuo, diluted with 2 mL of 1M HC1 and extracted 3 times with EtOAc. The organic layers were dried over sodium sulfate and

concentrated. The crude was purified by chromatography (CH ₂ Cl ₂ :MeOH 99.5:0.5) to afford 2- bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidine as a light yellow solid (1.86 g, 82%). MS (ES+) m/z: 315.0 and 317.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-2:

2-bromo-4-[4-(trifluoromethyl)phenyl]-6 7-dihyd

In analogy to the preparation of the intermediate 15-1, starting from 4- (trifluoromethyl) aniline was prepared 32 mg of the intermediate 2-bromo-4-[4-(trifluoromethyl)phenyl]-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-2) as a white solid. MS (ES+) m/z: 347.0 and 349.0 [M+H] ⁺ . (Br isotopes). Intermediate 15-3:

2-bromo-4-(3,5-difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazol o[l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 3,5-difluoroaniline was prepared 234 mg of the intermediate 2-bromo-4-(3,5-difluorophenyl)-6,7-dihydro-5H-

[l,2,4]triazlo[l,5-a]pyrimidine (15-3) as a white solid. MS (ES+) m/z: 315.0 and 317.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-4:

2-bromo-4-(3-fluoro-4-methyl-phenyl)-6,7-dihydro-5H-[l,2,4]t riazolo[l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 3-fluoro-4-methyl-aniline was prepared 662 mg of the intermediate 2-bromo-4-(3-fluoro-4-methyl-phenyl)-6,7-dihydro- 5H-[l,2,4]triazolo[l,5-a]pyrimidine (15-4) as a light yellow oil. MS (ES+) m/z: 311.0 and 313.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-5:

2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H-[l,2,4]tria zolo[l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 2,3,4-trifluoroaniline was prepared 134 mg of the intermediate 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) as a light brown solid. MS (ES+) m/z: 333.0 and 335.0 [M+H] ⁺ . (Br isotopes). Intermediate 15-6:

2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 3-fluoroaniline was prepared 210 mg of the intermediate 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5- a]pyrimidine (15-6) as a light yellow solid. MS (ES+) m/z: 297.0 and 299.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-7:

2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo [l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 4-fluoroaniline was prepared 1.11 g of the intermediate 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5- a]pyrimidine (15-7) as a light yellow solid. MS (ES+) m/z: 297.0 and 299.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-8:

2-bromo-4-(3-chlorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 3-chloroaniline was prepared 1.06 g of the intermediate 2-bromo-4-(3-chlorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-8) as a white solid. MS (ES+) m/z: 313.0 and 315.0 [M+H] ⁺ . (Br isotopes). Intermediate 15-9:

2-bromo-4-(2-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 2-fluoroaniline was prepared 1.05 g of the intermediate 2-bromo-4-(2-fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5- a]pyrimidine (15-9) as a white solid. MS (ES+) m/z: 297.1 and 299.1 [M+H] ⁺ . (Br isotopes).

Intermediate 15-10:

2-bromo-4-[2-(trifluoromethyl)phenyl]-6,7-dihydro-5H-[l,2,4] triazolo[l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 2- (trifluoromethyl) aniline was prepared 0.90 g of the intermediate 2-bromo-4-[2-(trifluoromethyl)phenyl]-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-10) as a white solid. MS (ES+) m/z: 347.1 and 349.1

[M+H] ⁺ . (Br isotopes).

Intermediate 15-11:

2-bromo-4-(4-chlorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 4-chloroaniline was prepared 1.2 g of the intermediate 2-bromo-4-(4-chlorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-11) as a white solid. MS (ES+) m/z: 313.1 and 315.1

[M+H] ⁺ . (Br isotopes).

Intermediate 15-12:

2-bromo-4-phenyl-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyr imidine

In analogy to the preparation of the intermediate 15-1, starting from aniline was prepared 240 mg of the intermediate 2-bromo-4-phenyl-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi dine (15-12) as a white solid. MS (ES+) m/z: 279.0 and 281.0 [M+H] ⁺ . (Br isotopes).

Intermediate 15-13:

2-bromo-4-(4-methoxyphenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l ,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 4-methoxyaniline was prepared 1.05 g of the intermediate 2-bromo-4-(4-methoxyphenyl)-6,7-dihydro-5H-

[l,2,4]triazolo[l,5-a]pyrimidine (15-13) as a white solid. MS (ES+) m/z: 309.1 and 311.1

[M+H] ⁺ . (Br isotopes).

Intermediate 15-14:

2-bromo-4-[4-(trifluoromethoxy)phenyl]-6,7-dihydro-5H-[l, 2,4]triazolo[l,5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 4- (trifluoromethoxy) aniline was prepared 1.10 g of the intermediate 2-bromo-4-[4-(trifluoromethoxy)phenyl]-6,7-dihydro- 5H-[l,2,4]triazolo[l,5-a]pyrimidine (15-14) as a white solid. MS (ES+) m/z: 363.1 and 365.1 [M+H] ⁺ . (Br isotopes).

Intermediate 15-15:

2-bromo-4-(2-chlorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l, 5-a]pyrimidine

In analogy to the preparation of the intermediate 15-1, starting from 2-chloroaniline was prepared 1.06 g of the intermediate 2-bromo-4-(2-chlorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-15) as a white solid. MS (ES+) mJz: 313.0 and 315.0 [M+H] ⁺ . (Br isotopes).

Intermediates of type 20

Intermediate 20-1:

2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro-[l,2,4]tri azolo[l,5-a][l,3]diazepine

Step 1: 3,4-Difluoroaniline (3.00 g, 23.20 mmol) and diphenyl cyanocarbonimidate (5.53 g, 23.20 mmol) were dissolved in 2-propanol (64.00 mL). The reaction mixture was stirred at RT overnight. The crude was evaporated in vacuo and purified by column chromatography (Hept:EtOAc 100:0 to 50:50) to afford (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl) carbamimidate as a white solid (5.00 g, 79%). MS (ES+) mJz: 2Ί4Λ [M+H] ⁺ .

Step 2: A solution of (Z)-phenyl N'-cyano-N-(3,4-difluorophenyl)carbamimidate (10.0 g, 36.6 mmol), 2-(3-bromobutoxy)tetrahydro-2H-pyran (13.30 g, 54.90 mmol) and K ₂ C0 ₃ (10.10 g, 73.20 mmol) in DMF (350 mL) was heated overnight at 85°C. The reaction mixture was concentrated in vacuo and the residue was purified by column chromatography (Hept:EtOAc 90:10 to 50:50) to give 3-cyano-l-(3,4-difluorophenyl)-2-phenyl-l-(4-tetrahydropyran -2- yloxybutyl)isourea as a colorless oil (5.31 g, 34%). MS (ES+) mJz: 430.2 [M+H] ⁺ . Step 3: To a solution of 3-cyano-l-(3,4-difluorophenyl)-2-phenyl-l-(4-tetrahydropyran -2- yloxybutyl)isourea (5.29 g, 12.30 mmol) in MeOH (40 mL) was added hydrazine hydrate 25% in water (2.47 g, 2.44 mL, 12.30 mmol). The reaction mixture was stirred at RT for 7 hours, evaporated and purified by column chromatography (CH ₂ Cl ₂ :MeOH 99: 1 to 92.5:7.5) to afford N3-(3,4-difluorophenyl)-N3-(3-tetrahydropyran-2-yloxybutyl)- 4H-l,2,4-triazole-3,5-diamine as a colourless oil (3.54 g, 78%). MS (ES+) m/z: 368.2 [M+H] ⁺ .

Step 4: To a solution of N3-(3,4-difluorophenyl)-N3-(3-tetrahydropyran-2-yloxybutyl)- 4H- 1,2,4- triazole-3,5-diamine (3.50 g, 9.53 mmol) in MeOH (85 mL) was added an aqueous HC1 2M solution (17 mL). The reaction mixture was stirred at RT for 90 minutes and concentrated in vacuo. The residue was diluted with EtOAc and washed with an aqueous NaHC0 ₃ solution. The organic layer was dried on Na ₂ S0 ₄ and the product purified by combiflash chromatography to afford 4-(N-(5-amino-4H-l,2,4-triazol-3-yl)-3,4-difluoro-anilino)bu tan-l-ol as a white solid (2.51 g, 93%). MS (ES+) m/z: 284.1 [M+H] ⁺ .

Step 5: At 0°C, cyanomethylenetrimethylphosphorane 0.5 M in THF (8.47 mL, 4.24 mmol) was added drop wise within 15 minutes to a solution of 4-((5-amino-4H-l,2,4-triazol-3-yl)(3,4- difluorophenyl)amino)butan-l-ol (1.00 g, 3.53 mmol) in THF (120 mL) at 0°C and stirred at RT overnight. The mixture was concentrated under vacuo, and the crude diluted with EtOAc and washed with water. The organic layer was dried over sodium sulfate, filtered and evaporated in vacuo. The crude was purified using silica chromatography (CH ₂ Cl ₂ :MeOH 99: 1 to 96:4) to afford 4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro-[l,2,4]triazolo[l, 5-a][l,3]diazepin-2-amine as a white solid (0.2 g, 21%). MS (ES+) m/z: 266.1 [M+H] ⁺ . Step 6: To a black solution of iert-butyl nitrite (115 mg, 0.13 mL, 1.01 mmol) and cupric bromide (225 mg, 47.7 μΐ, 1.01 mmol) in CH ₃ CN (15 mL) at 60°C, 4-(3,4-difluorophenyl)- 5,6,7, 8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin-2-amine (178 mg, 0.671 mmol,) in 25 mL CH ₃ CN was added drop wise. After addition, the reaction mixture was heated to 75°C and stirred for 30 minutes. The reaction mixture was concentrated in vacuo, diluted with 2 mL of 1M HC1 and extracted 3 times with EtOAc. The organic layers were dried over sodium sulfate and concentrated. The crude was purified by chromatography (CH ₂ Cl ₂ :MeOH 99.5:0.5) to afford 2- bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepine as a light yellow oil (0.13 g, 58%). MS (ES+) m/z: 329.0 and 331.0 [M+H] ⁺ . (Br isotopes). Intermediate 20-2:

2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydro-[l, 2,4]triazolo[l,5- a][l,3]diazepine

In analogy to the preparation of the intermediate 20-1, starting from 4- (trifluoromethyl) aniline was prepared 72 mg of the intermediate 2-bromo-4-[4-(trifluoromethyl)phenyl]-5, 6,7,8- tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepine (20-2) as a white solid. MS (ES+) m/z: 361.0 and 363.0 [M+H] ⁺ . (Br isotopes).

Intermediates of type 10

Intermediate 10-1:

(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1]oct an-8-amine

Step 1: In a sealed tube tert-butyl N-[(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (500 mg, 2.21 mmol) was dissolved in EtOH (10 mL) and 4-chloro-6-methylpyrimidine (869 mg, 6.63 mmol) was added followed by triethylamine (894 mg, 1.23 mL, 8.84 mmol). The reaction mixture was stirred at 130°C overnight. The crude reaction mixture was concentrated in vacuum. The residue was diluted with 20 mL of CH ₂ CI ₂ and 20 mL of water. The organic phase was extracted with CH ₂ CI ₂ (3 x 20 mL), dried over MgS0 ₄ and concentrated in vacuum. The crude material was purified by flash chromatography (0 % to 100 % EtOAc in heptane) to afford tert- butyl N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]carbamate as a yellow solid (496 mg, 71 % yield) . MS (ES+) m/z: 319.2 [(M+H) ⁺ ]

Step 2: To a light yellow solution of tert-butyl N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-yl]carbamate (260 mg, 817 μιηοΐ) in CH ₂ CI ₂ (8 mL) was added TFA (931 mg, 629 μΐ, 8.17 mmol). The reaction mixture was stirred at room temperature over night and concentrated in vacuum. The crude material was purified by Ion-exchange column (Si-SCX- 2, 10 g, washed with MeOH and liberated with MeOH (NH ₃ 2M)) to afford (lR,5S,8S)-3-(6- methylpyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-amine 10-1 (195 mg, 804 μιηοΐ, 98.5 % yield) that was used in the next step without further purification. MS (ES+) m/z: 219.2 [(M+H) ⁺ ] Intermediate 10-2:

(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azabicyclo [3.2.1]octan-8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (200 mg, 884 μιηοΐ) and 4-chloro-5- fluoro-6-methylpyrimidine (194 mg, 1.33 mmol) in a sealed tube at 100 °C and EtOH as solvent in the presence of triethylamine (358 mg, 493 μΐ, 3.53 mmol), tert-butyl N-[(lR,5S,8S)-3-(5- fluoro-6-methyl-pyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-y l]carbamate was obtained as a white solid (255 mg, 758 μηιοΐ, 86 % yield). MS (ES+) m/z: 337.3 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azabicyclo[3.2.1]octa n-8-yl]carbamate (253 mg, 752 μιηοΐ) in CH ₂ C1 ₂ in the presence of aqueuous HC1 37 % (445 mg, 371 μΐ, 4.51 mmol),

(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azabicy clo[3.2.1]octan-8-amine (170 mg, 719 μιηοΐ, 96 % yield) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 237.1 [(M+H) ⁺ ].

Intermediate 10-3:

(lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2.1]oct an-8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (250 mg, 1.1 mmol) and 4-chloro-6- fluoro-pyrimidine (220 mg, 1.66 mmol) in a sealed tube at 100 °C using EtOH as solvent in presence of triethylamine (447 mg, 616 μΐ, 4.42 mmol), tert-butyl N-[(lR,5S,8S)-3-(6- chloropyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-yl]carbamat e (329 mg, 88 % yield) was obtained as a white solid. MS (ES+) m/z: 339.2 [(M+H) ⁺ ]. Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-yl]car bamate (325 mg, 959 μιηοΐ) in CH ₂ C1 ₂ in the presence of HC1 37 % (567 mg, 473 μΐ, 5.76 mmol), (lR,5S,8S)-3-(6- chloropyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-amine (230 mg, 100 % yield) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 239.2 [(M+H) ⁺ ].

Intermediate 10-4:

(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3-azabicyclo[3.2.1]oc tan-8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (250 mg, 1.1 mmol) and 4-iodo-6- methoxypyrimidine (391 mg, 1.66 mmol) in a sealed tube at 100 °C using DMF as solvent in the presence of K ₂ C0 ₃ (458 mg, 3.31 mmol), tert-butyl N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (315 mg, 85 % yield) was obtained as a white solid. MS (ES+) m/z 335.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)-

3- (6-methoxypyrimidin-4-yl)-3-azabicyclo[3.2.1]octan-8-yl]carb amate (330 mg, 987 μιηοΐ) in CH ₂ CI ₂ in the presence of TFA (1.13 g, 760 μΐ, 9.87 mmol), (lR,5S,8S)-3-(6-methoxypyrimidin-

4- yl)-3-azabicyclo[3.2.1]octan-8-amine (222 mg, 96 % yield) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 235.2 [(M+H) ⁺ ].

Intermediate 10-5:

(lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo [3.2.1]octan-8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (1.57 g, 6.87 mmol) and 4-iodo-2- (trifluoromethyl)pyridine (1.5 g, 5.33 mmol) in a sealed tube at 150 °C using NMP as solvent in the presence of DIPEA (964 mg, 1.3 ml, 7.46 mmol), tert-butyl N-[(lR,5S,8S)-3-[2-

(trifluoromethyl)-4-pyridyl]-3-azabicyclo[3.2.1]octan-8-y l]carbamate (1.37 g, 70 % yield) was obtained as a white solid. MS (ES+) m/z: 372.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo[3.2.1]octan-8 -yl]carbamate (1.05 g, 2.82 mmol) in CH ₂ C1 ₂ in the presence of HC1 37 % (1.68 g, 1.4 mL, 17 mmol), (lR,5S,8S)-3-[2- (trifluoromethyl)-4-pyridyl]-3-azabicyclo[3.2.1]octan-8-amin e (735 mg, 96 % yield) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 272.2 [(M+H) ⁺ ].

Intermediate 10-6:

(lR,5S,8S)-3-(2-chloro-4-pyridyl)-3-azabicyclo[3.2.1]octan-8 -amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N-

[(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (120 mg, 0.53 mmol) and 2-chloro-4- fluoro-pyridine (76 mg, 0.58 mmol) in a sealed tube at 150 °C using NMP as solvent in the presence of DIPEA (137 mg, 0.185 ml, 1.06 mmol), tert-butyl N-[(lR,5S,8S)-3-(2-chloro-4- pyridyl)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (150 mg, 82 % yield) was obtained as a white solid. MS (ES+) m/z 338.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo[3.2.1]octan-8 -yl]carbamate (147 mg, 435 μιηοΐ) in CH ₂ C1 ₂ in the presence of HC1 37 % (257 mg, 214 μΐ, 2.61 mmol), (lR,5S,8S)-3-(2-chloro-4- pyridyl)-3-azabicyclo[3.2.1]octan-8-amine (90 mg, 87 % yield) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 238.1 [(M+H) ⁺ ]. Intermediate 10-7:

(lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-azabicyclo[3.2.1]octan- 8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (2.00 g, 8.84 mmol) and 4-fluoro-2- methoxypyridine (1.12 g, 8.84 mmol) in a sealed tube at 140 °C using NMP as solvent in the presence of DIPEA (2.28 g, 3.09 mL, 17.70 mmol), tert-butyl N-[(lR,5S,8S)-3-(2-methoxy-4- pyridyl)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (1.42 g, 48%) was obtained as a white solid. MS (ES+) m/z: 334.3 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-(2-methoxy-4-pyridyl)-3-azabicyclo[3.2.1]octan-8-yl]carbam ate (1.42 g, 4.26 mmol) in CH ₂ C1 ₂ in the presence of TFA (7.38 g, 5.0 mL, 15.2 mmol), (lR,5S,8S)-3-(2-methoxy-4- pyridyl)-3-azabicyclo[3.2.1]octan-8-amine (0.89 g, 89%) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 234.2 [(M+H) ⁺ ].

Intermediate 10-8:

(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1]oct an-8-amine

Step 1: In analogy to the preparation of the intermediate 10-1 (step 1) from tert-butyl N- [(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (2.00 g, 8.84 mmol) and 3,5- dichloropyridazine (2.0 g, 13.4 mmol) in a sealed tube at 90 °C using EtOH as solvent in the presence of Et ₃ N (3.63 g, 5.0 mL, 35.9 mmol), tert-butyl N-[(lR,5S,8S)-3-(6-chloropyridazin-4- yl)-3-azabicyclo[3.2.1]octan-8-yl]carbamate (1.71 g, 54%) was obtained as a white solid. MS (ES+) m/z: 339.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1]octan-8-yl]car bamate (0.93 g, 2.72 mmol) in CH ₂ C1 ₂ in the presence of HC1 37% (1.61 g, 1.34 mL, 16.3 mmol), (lR,5S,8S)-3-(6- chloropyridazin-4-yl)-3-azabicyclo[3.2.1]octan-8-amine (0.65 g, 100%) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 239.1

[(M+H) ⁺ ].

Intermediate 10-9:

( xypyridazin-4-yl)-3-azabicyclo[3.2.1]octan-8-amine

Step 1: To a solution of tert-butyl N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]carbamate (963 mg, 2.70 mmol) in MeOH (22 mL) in a sealed tube was added a methanol solution of NaOMe (25%, 1.9 mL, 8.3 mmol). The reaction mixture was heated at 85 °C over night. The reaction mixture was adsorbed on Isolute HM-N and a column

chromatography gave tert-butyl N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3-azabicyclo[3.2.1 ] octan-8-yl]carbamate (362 mg, 38%) as a white solid. MS (ES+) m/z: 335.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl N-[(1R,5S,8S)- 3-(6-methoxypyridazin-4-yl)-3-azabicyclo[3.2.1]octan-8-yl]ca rbamate (0.93 g, 2.72 mmol) in CH ₂ CI ₂ in the presence of TFA (1.12 g, 0.76 mL, 9.86 mmol), (lR,5S,8S)-3-(6- methoxypyridazin-4-yl)-3-azabicyclo[3.2.1]octan-8-amine (225 mg, 96%) was obtained as a white solid and used directly in the next step without further purification. MS (ES+) m/z: 235.2 [(M+H) ⁺ ].

Intermediate 10-10:

(lR,5S,8S)-3-(3-methyl-l,2,4-oxadiazol-5-yl)-3-azabicyclo[3. 2.1]octan-8-amine

Step 1: To a light yellow solution of tert-butyl N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3- azabicyclo[3.2.1] octan-8-yl]carbamate (250 mg, 1.1 mmol), in EtOH (4 mL) was added sodium bicarbonate (102 mg, 1.22 mmol) followed by cyanogen bromide (129 mg, 1.22 mmol). The reaction was stirred over night at room temperature and the suspension was filtered off and washed with some EtOH. The crude reaction mixture was concentrated in vacuum and the residue was purified by flash chromatography (silica gel, 12 g, 0 % to 100 % EtOAc in heptane) to afford tert-butyl N-[(lR,5S,8S)-3-cyano-3-azabicyclo[3.2.1]octan-8-yl]carbamat e as a light yellow solid (216 mg, 78%). MS (ES+) m/z: 252.2 [(M+H) ⁺ ].

Step 2: Tert-butyl N-[(lR,5S,8S)-3-cyano-3-azabicyclo[3.2. l]octan-8-yl]carbamate (200 mg, 796 μιηοΐ) was dissolved in EtOH (20 mL) and N-hydroxyacetimidamide ((70.7 mg, 955 μιηοΐ) and zinc chloride ((130 mg, 955 μιηοΐ) were added. The reaction mixture was stirred at room temperature for 2 hours. HCl 37 % (199 μΐ, 2.39 mmol) was added and the reaction mixture was warmed and stirred at 60 ⁰ for 3 hours. The solvent was removed in vacuum. The residue was taken up with 25 mL sat. NaHC0 ₃ and extracted with CH ₂ CI ₂ (3 x 25 mL). The organic layers were dried over Na ₂ S0 ₄ and concentrated in vacuum. The crude material was purified by flash chromatography (silica gel, 0 % to 10 % MeOH in CH ₂ C1 ₂ , at the end 7M NH ₃ in MeOH was used) to afford (lR,5S,8S)-3-(3-methyl-l,2,4-oxadiazol-5-yl)-3-azabicyclo[3. 2.1]octan-8-amine as an off-white powder (126 mg, 76 % yield). MS (ES+) m/z: 209.1 [(M+H) ⁺ ].

General procedure 1: Buchwald coupling reaction

To a solution of an intermediate 9, 15 or 20 in 1,4-dioxane was added 1.1 equivalent of an intermediate 10. The reaction mixture was degased and a palladium catalyst [either dibromo-bis- (tritert.-butyl)-phosphine -palladium (0.1 eq. CAS 185812-86-6) or tri(dibenzylidenacetonne) dipalladium(O) CAS51364-51-3 in the presence of 2-di-tert-butylphosphino-2',4',6'- triisopropylbiphenyl CAS564483-19-8 ] and NaOtBu (2.1 eq.) were added. The reaction mixture was heated at 100°C until completion of the reaction (usually between 2 and 8 hours) and concentrated under vacuo. A purification was done either by column chromatography or reverse phase preparative HPLC to afford the desired product. Example 1

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H-

[l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 13 mg of the title compound as a white solid. MS (ES+) m/z 506.2 [(M+H) ⁺ ].

Example 2

N-[(lR,5S,8S)-3-(2-chloro-4-pyridyl)-3-azabicyclo[3.2.1]o ctan-8-yl]-4-(3,4-difluorophenyl)-

6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(2-chloro-4-pyridyl)-3- azabicyclo[3.2.1]octan-8-amine (10-6) was prepared 15 mg of the title compound as a white solid. MS (ES+) m/z: 472.1 [(M+H) ⁺ ].

Example 3

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan- 8-yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5 -a] pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 26 mg of the title compound as a white solid. MS (ES+) m/z: 453.2 [(M+H) ⁺ ] .

Example 4

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-5,6-dihydroimidazo[l,2-b][l,2,4 ]triazol-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6-dihydroimidazo[l,2- b][l,2,4]triazole (9-1) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo[3. 2.1] octan-8-amine (10-5) was prepared 40 mg of the title compound as a white solid. MS (ES+) m/z 492.3 [(M+H) ⁺ ].

Example 5

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-

8-yl]-5,6-dihydroimidazo[l,2-b][l,2,4]triazol-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6-dihydroimidazo[l,2- b][l,2,4]triazole (9-1) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1]oct an-8- amine (10-1) was prepared 24 mg of the title compound as a white solid. MS (ES+) m/z: 439.3 [(M+H) ⁺ ].

Example 6

4-[4-(trifluoromethyl)phenyl]-N-[(lR,5S,8S)-3-[2-(trifluorom ethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-[4-(trifluoromethyl)phenyl]-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-2) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z: 538.2 [(M+H) ⁺ ].

Example 7

4-[4-(trifluoromethyl)phenyl]-N-[(lR,5S,8S)-3-[2-(trifluorom ethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-2) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z 552.2 [(M+H) ⁺ ].

Example 8

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5- a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-[4-(trifluoromethyl)phenyl]-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-2) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 21 mg of the title compound as a white solid. MS (ES+) m/z 484.2 [(M+H) ⁺ ].

Example 9

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[ l,5-a][l,3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-2) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 19 mg of the title compound as a white solid. MS (ES+) m/z 499.2 [(M+H) ⁺ ].

Example 10

4-(3-fluoro-4-methyl-phenyl)-N-[(lR,5S,8S)-3-[2-(trifluorome thyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluoro-4-methyl-phenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-4) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 34 mg of the title compound as a white solid. MS (ES+) m/z: 502.2 [(M+H) ⁺ ].

Example 11

4-(3-fluoro-4-methyl-phenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimi din-4-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluoro-4-methyl-phenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-4) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 29 mg of the title compound as a white solid. MS (ES+) m/z: 449.2 [(M+H) ⁺ ].

Example 12

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-[4- (trifluoromethyl)phenyl]-5,6-dihydroimidazo[l,2-b][l,2,4]tri azol-2-amine

Using the general procedure 1, from 2-bromo-4-[4-(trifluoromethyl)phenyl]-5,6-dihydroimidazo [l,2-b][l,2,4]triazole (9-2) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-amine (10-1) was prepared 35 mg of the title compound as a white solid. MS (ES+) m/z: All [(M+H) ⁺ ].

Example 13

N-[(lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3-fluoro-4- methyl-phenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidi n-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluoro-4-methyl-phenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-4) and (lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-3) was prepared 4 mg of the title compound as a white solid. MS (ES+) m/z: 469.2 [(M+H) ⁺ ] .

Example 14

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4 -yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-4) was prepared 29 mg of the title compound as a white solid. MS (ES+) m/z: 469.2 [(M+H) ⁺ ].

Example 15

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(3-methyl-l,2,4-oxadi azol-5-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(3-methyl-l,2,4-oxadiazol-5-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-10) was prepared 16 mg of the title compound as a white solid. MS (ES+) m/z: 443.2 [(M+H) ⁺ ].

Example 16

N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3,4- difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimid in-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo [3.2.1]octan-8-amine (10-8) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z: 473.1 [(M+H) ⁺ ].

Example 17

N-[(lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3,4- difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimid in-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(6-chloropyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-3) was prepared 4 mg of the title compound as a white solid. MS (ES+) m/z: 473.1 [(M+H) ⁺ ].

Example 18

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazi n-4-yl)-3-azabicyclo[3.2.1]octan- 8-yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5 -a] pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-9) was prepared 24 mg of the title compound as a white solid. MS (ES+) m/z 469.2 [(M+H) ⁺ ] .

Example 19

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(5-fluoro-6-methyl-py rimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H-

[l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-2) was prepared 9 mg of the title compound as a white solid. MS (ES+) m/z: 471.2 [(M+H) ⁺ ].

Example 20

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyridazin-4- yl)-3-azabicyclo[3.2.1]octan- 8-yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5 -a] pyrimidin-2-amine

Step 1: Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) andtert-butyl (lR,5S,8S)-8-amino-3-azabicyclo[3.2.1] octane-3-carboxylate (commercially available) was prepared 130 mg of tert-butyl (lR,5S,8S)-8- [[4-(3,4-difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5- a]pyrimidin-2-yl]amino]-3- azabicyclo[3.2.1]octane-3-carboxylate as a white solid. MS (ES+) m/z: 461.2 [(M+H) ⁺ ].

Step 2: In analogy to the preparation of intermediate 10-1 (step 2) from tert-butyl (lR,5S,8S)-8- [[4-(3,4-difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5- a]pyrimidin-2-yl]amino]-3- azabicyclo[3.2.1]octane-3-carboxylate (128 mg, 0.278 mmol) in CH ₂ C1 ₂ in the presence of TFA (475 mg, 0.321 mL, 4.17 mmol), N-[(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]-4-(3,4- difluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimid in-2-amine (94 mg, 94%) was obtained as a light yellow oil and used directly in the next step without further purification. MS (ES+) m/z: 361.2 [(M+H) ⁺ ].

Step 3: To a solution of N-[(lR,5S,8S)-3-azabicyclo[3.2.1]octan-8-yl]-4-(3,4-difluoro phenyl)- 6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine (30 mg, 0.083 mmol) in NMP (1 mL) was added 5-chloro-3-methylpyridazine (10.7 mg, 0.083 mmol) and DIPEA (32.3 mg, 43.6 \L, 0.25 mmol). The reaction mixture was heated at 110°C for 4 hours, concentrated under vacuo before a purification by reverse phase preparative HPLC gave 4-(3,4-difluorophenyl)-N- [(lR,5S,8S)-3-(6-methylpyridazin-4-yl)-3-azabicyclo[3.2.1]oc tan-8-yl]-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidin-2-amine (4 mg, 12%) as a white solid. MS (ES+) m/z: 453.2 [(M+H) ⁺ ].

Example 21

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl) -3-azabicyclo[3.2.1]octan-8-

-dihydro-5H- [1 ,2,4] triazolo[ 1 ,5 -a] pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-1) and (lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-azabicyclo [3.2.1]octan-8-amine (10-7) was prepared 7 mg of the title compound as a white solid. MS (ES+) m/z: 468.2 [(M+H) ⁺ ].

Example 22

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 6 mg of the title compound as a white solid. MS (ES+) m/z: 520.2 [(M+H) ⁺ ] .

Example 23

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan- 8-yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin -2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z: 467.2 [(M+H) ⁺ ].

Example 24

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4 -yl)-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-4) was prepared 7 mg of the title compound as a white solid. MS (ES+) m/z: 483.2 [(M+H) ⁺ ].

Example 25

N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(3,4- difluorophenyl)-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l, 3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-8) was prepared 4 mg of the title compound as a white solid. MS (ES+) m/z: 4&Ί.2 [(M+H) ⁺ ].

Example 26

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(3-methyl-l,2,4-oxadi azol-5-yl)-3- azabicyclo[3.2.1]octan-8-yl]-5,6,7,8-tetrahydro-[l,2,4]triaz olo[l,5-a][l,3]diazepin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-(3-methyl-l,2,4-oxadiazol-5-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-10) was prepared 5 mg of the title compound as a white solid. MS (ES+) m/z: 457.2 [(M+H) ⁺ ].

Example 27

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4 -yl)-3-azabicyclo[3.2.1]octan- 8-yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin -2-amine

Using the general procedure 1, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) and (lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-9) was prepared 6 mg of the title compound as a white solid. MS (ES+) m/z: 483.2 [(M+H) ⁺ ].

Example 28

4-(3,4-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyridazin-4- yl)-3-azabicyclo[3.2.1]octan- 8-yl]-5,6,7,8-tetrahydro-[l,2,4]triazolo[l,5-a][l,3]diazepin -2-amine

In anlogy to example 20, from 2-bromo-4-(3,4-difluorophenyl)-5,6,7,8-tetrahydro- [l,2,4]triazolo[l,5-a][l,3]diazepine (20-1) was prepared 6 mg of the title compound as a white solid. MS (ES+) m/z: 467.2 [(M+H) ⁺ ].

Example 29

N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3-azabicyclo [3.2.1]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi din-2-amine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 22 mg of the title compound as a white solid. MS (ES+) m/z 524.0 [(M+H) ⁺ ].

Example 30

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi din-2-amine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 9 mg of the title compound as a white solid. MS (ES+) m/z: 471.2 [(M+H) ⁺ ].

Example 31

N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3-azabicyclo[3.2.1 ]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi din-2-amine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) and (lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-4) was prepared 10 mg of the title compound as a white solid. MS (ES+) m/z 487.2 [(M+H) ⁺ ].

Example 32

N-[(lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi din-2-amine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) and (lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-8) was prepared 22 mg of the title compound as a white solid. MS (ES+) m/z 491.1 [(M+H) ⁺ ].

Example 33

N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3-azabicyclo[3.2.1 ]octan-8-yl]-4-(2,3,4- trifluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimi din-2-amine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-5) and (lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-9) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z 487.2 [(M+H) ⁺ ].

Example 34

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-py ridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 20 mg of the title compound as a white solid. MS (ES+) m/z: 488.2 [(M+H) ⁺ ].

Example 35

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)- 3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 14 mg of the title compound as a white solid. MS (ES+) m/z: 435.2 [(M+H) ⁺ ].

Example 36

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-py ridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 14 mg of the title compound as a white solid. MS (ES+) m/z: 488.2 [(M+H) ⁺ ]. Example 37

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)- 3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 7 mg of the title compound as a white solid. MS (ES+) m/z: 435.2 [(M+H) ⁺ ].

Example 38

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4- yl)-3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-4) was prepared 11 mg of the title compound as a white solid. MS (ES+) m/z: 451.3 [(M+H) ⁺ ].

Example 39

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-a zabicyclo[3.2.1]octan-8-yl]- 6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3- azabicyclo[3.2.1]octan-8-amine (10-7) was prepared 7 mg of the title compound as a white solid. MS (ES+) m/z: 450.2 [(M+H) ⁺ ] .

Example 40

4-(3,5-difluorophenyl)-N-[(lR,5S,8S)-3-(6-methylpyrimidin-4- yl)-3-azabicyclo[3.2.1]octan- 8-yl] -6,7-dihydro-5H- [ 1 ,2,4] triazolo[ 1 ,5 -a] pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,5-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-3) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-1) was prepared 7 mg of the title compound as a white solid. MS (ES+) m/z: 453.2 [(M+H) ⁺ ].

Example 41

4-(3,5-difluorophenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)- 4-pyridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,5-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-3) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 8 mg of the title compound as a white solid. MS (ES+) m/z: 506.2 [(M+H) ⁺ ].

Example 42

4-(4-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl) -3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-(6-methoxypyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-9) was prepared 9 mg of the title compound as a white solid. MS (ES+) m/z: 451.2 [(M+H) ⁺ ].

Example 43

N-[(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azabicy clo[3.2.1]octan-8-yl]-4-(4- fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin -2-amine

Using the general procedure 1, from 2-bromo-4-(4-fluorophenyl)-6,7-dihydro-5H-

[l,2,4]triazolo[l,5-a]pyrimidine (15-7) and (lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-2) was prepared 9 mg of the title compound as a white solid. MS (ES+) m/z: 453.2 [(M+H) ⁺ ].

Example 44

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyridazin-4-yl) -3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-(6-chloropyridazin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-8) was prepared 12 mg of the title compound as a white solid. MS (ES+) m/z: 451.2 [(M+H) ⁺ ] .

Example 45

N-[(lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3-azabicy clo[3.2.1]octan-8-yl]-4-(3- fluorophenyl)-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin -2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H-

[l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-(5-fluoro-6-methyl-pyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-2) was prepared 8 mg of the title compound as a white solid. MS (ES+) m/z: 453.2 [(M+H) ⁺ ].

Example 46

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-a zabicyclo[3.2.1]octan-8-yl]-

6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3- azabicyclo[3.2.1]octan-8-amine (10-7) was prepared 36 mg of the title compound as a white solid. MS (ES+) m/z 450.2 [(M+H) ⁺ ]. Example 47

4-(3-fluorophenyl)-N-[(lR,5S,8S)-3-(6-methoxypyrimidin-4-yl) -3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3-fluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-6) and (lR,5S,8S)-3-(6-methoxypyrimidin-4-yl)-3- azabicyclo[3.2.1]octan-8-amine (10-4) was prepared 3 mg of the title compound as a white solid. MS (ES+) m/z: 451.2 [(M+H) ⁺ ].

Example 48

N-[(lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1] octan-8-yl]-4-(2,3,4- trifluorophenyl)-5,6-dihydroimidazo[l,2-b][l,2,4]triazol-2-a mine

Using the general procedure 1, from 2-bromo-4-(2,3,4-trifluorophenyl)-5,6-dihydroimidazo[l,2- b][l,2,4]triazole (9-3) and (lR,5S,8S)-3-(6-methylpyrimidin-4-yl)-3-azabicyclo[3.2.1]oct an-8- amine (10-1) was prepared 40 mg of the title compound as a white solid. MS (ES+) m/z: 457.3 [(M+H) ⁺ ].

Example 49

4-(3,5-difluorophenyl)-N-[(lR,5S,8S)-3-(2-methoxy-4-pyridyl) -3-azabicyclo[3.2.1]octan-8- yl]-6,7-dihydro-5H-[l,2,4]triazolo[l,5-a]pyrimidin-2-amine

Using the general procedure 1, from 2-bromo-4-(3,5-difluorophenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-3) and (lR,5S,8S)-3-(2-methoxy-4-pyridyl)-3-azabicyclo [3.2.1]octan-8-amine (10-7) was prepared 6 mg of the title compound as a white solid. MS (ES+) m/z 468.2 [(M+H) ⁺ ].

Example 50

4-(4-methoxyphenyl)-N-[(lR,5S,8S)-3-[2-(trifluoromethyl)-4-p yridyl]-3- azabicyclo[3.2.1]octan-8-yl]-6,7-dihydro-5H-[l,2,4]triazolo[ l,5-a]pyrimidin-2-amine e

Using the general procedure 1, from 2-bromo-4-(4-methoxyphenyl)-6,7-dihydro-5H- [l,2,4]triazolo[l,5-a]pyrimidine (15-13) and (lR,5S,8S)-3-[2-(trifluoromethyl)-4-pyridyl]-3- azabicyclo[3.2.1]octan-8-amine (10-5) was prepared 48 mg of the title compound as a white solid. MS (ES+) m/z: 500.2 [(M+H) ⁺ ].