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Title:
DIALKYLAMINOARYLPIPERIDINYL-O-PHENOXY AND O-BENZYLOXYPROPYLAMINO DERIVATIVES HAVING MULTIMODAL ACTIVITY AGAINST PAIN
Document Type and Number:
WIPO Patent Application WO/2019/115008
Kind Code:
A1
Abstract:
The present invention relates to dialkylaminoarylpiperidinyl-o-phenoxy and obenzyloxypropylamino derivatives having dual pharmacological activity towards both the α2δ subunit, in particular the α2δ-1 subunit, of the voltage-gated calcium channel and the μ-opioid receptor, to processes of preparation of such compounds, to pharmaceutical compositions comprising them, and to their use in therapy, in particular for the treatment of pain.

Inventors:
ALMANSA-ROSALES CARMEN (ES)
VIRGILI-BERNADÔ MARINA (ES)
ALONSO-XALMA MONICA (ES)
Application Number:
EP2018/000554
Publication Date:
June 20, 2019
Filing Date:
December 11, 2018
Export Citation:
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Assignee:
ESTEVE PHARMACEUTICALS SA (ES)
International Classes:
C07D401/12; A61K31/4468; A61K31/4535; A61K31/4545; A61P25/04; C07D211/58; C07D401/14
Domestic Patent References:
WO2017191304A12017-11-09
Foreign References:
US20100311782A12010-12-09
Other References:
TURK, D.C.; WILSON, H.D.; CAHANA, A., LANCET, vol. 377, 2011, pages 2226 - 2235
GOLDBERG, D.S.; MCGEE, S.J., BMC PUBLIC HEALTH, vol. 11, 2011, pages 770
ZAMPONI ET AL., PHARMACOL REV., vol. 67, 2015, pages 821 - 70
PERRET; LUO, NEUROTHERAPEUTICS, vol. 6, 2009, pages 679 - 92
NEUMAIER ET AL., PROG NEUROBIOL., vol. 129, 2015, pages 1 - 36
VINK; ALEWOOD, BR J PHARMACOL., vol. 167, 2012, pages 970 - 89
DAVIES ET AL., TRENDS PHARMACOL SCI., vol. 28, 2007, pages 220 - 8
DOLPHIN AC, NAT REV NEUROSCI., vol. 13, 2012, pages 542 - 55
BIOCHIM BIOPHYS ACTA, vol. 1828, 2013, pages 1541 - 9
"Opioids and Pain Relief: A Historical Perspective. Progress in Pain Research and Management", vol. 25, 2003, IASP PRESS
DICKENSON, A.H.; SUZUKI, R.: "Opioids in neuropathic pain: Clues from animal studies", EUR J PAIN, vol. 9, 2005, pages 113 - 6, XP004767581, DOI: doi:10.1016/j.ejpain.2004.05.004
LEHAR ET AL., NAT BIOTECHNOL, vol. 27, 2009, pages 659 - 666
GILRON ET AL., LANCET NEUROL., vol. 12, no. 11, November 2013 (2013-11-01), pages 1084 - 95
SCHRODER ET AL., J PHARMACOL EXP THER., vol. 337, 2011, pages 312 - 20
J PHARMACOL EXP THER., vol. 342, 2012, pages 232
ZHANG ET AL., CELL DEATH DIS., vol. 5, 2014, pages e1138
HOPKINS, NAT CHEM BIOL., vol. 4, 2008, pages 682 - 90
MAO, J.; GOLD, M.S.; BACKONJA, M., J. PAIN, vol. 12, 2011, pages 157 - 166
BORNOT A; BAUER U; BROWN A; FIRTH M; HELLAWELL C; ENGKVIST O: "Systematic Exploration of Dual-Acting Modulators from a Combined Medicinal Chemistry and Biology Perspective", J. MED. CHEM, vol. 56, 2013, pages 1197 - 1210
Attorney, Agent or Firm:
PETERS, Hajo et al. (DE)
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Claims:
CLAIMS:

1. Compound of general formula (I),

wherein

X is selected from a bond, -[C(RaRb)]p-, -[CH2]PC(0)[CH2]q-,

[CH2]pC(0)N(Rz)[CH2]q-, -[CH2]pN(Rz)C(0)[CH2]q- and -[CH2]PN(Rz)[CH2]q-;

Ra is selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-e alkynyl;

Rb is selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Ra and Rb, taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

Rz is selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is O, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(Rio -io')-; wherein R10 and Rio· are independently selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C2.6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rio and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y2 is— C(Rio”Rio")-; wherein Rio- and Rio - are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-e alkynyl; alternatively, RKT and Rur may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs·, Rs- and Rs · are independently selected from hydrogen, halogen, substituted or unsubstituted Ci.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R5 and Rs· and/or Rs- and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-e alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Re and Re· and/or R6· and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Ra and Ra· and/or Ra- and Ra- taken together with the carbon atom to which they are attached may form a carbonyl group;

R7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Ra is selected from substituted or unsubstituted Ci-a alkyl, substituted or unsubstituted C2-a alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Ra· is selected from hydrogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and Ra· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl,

R3 is selected from substituted or unsubstituted Ci-a alkyl, substituted or unsubstituted C2-e alkenyl, and substituted or unsubstituted C2-e alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; .

R3' is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-e alkenyl, and substituted or unsubstituted C2-e alkynyl; R4 and R4 are independently selected from halogen, -R4I , -OR4I , -NO2, - wherein R4I , R4r and R r are independently selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C2-e alkenyl and substituted or unsubstituted C2-6 a!kyny!; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

2. Compound according to claim 1 wherein R2 is a substituted or unsubstituted group selected from phenyl and thienyl.

3. Compound according to any one of claims 1 or 2 wherein the compound of Formula (I) is a compound of Formula (G), (la), (I3’), (lb) or (lb),

(lb),

(lb ), wherein R9 and Rg· are independently selected from hydrogen, halogen, -R21, - OR21, -NO2, -NR21R21’, -NR2iC(0)R2r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2i'R2r, -SR21 , -S(0)R2i, -S(0)2R2i , -CN, haloalkyl, haloalkoxy, - C(0)0R2I , -C(0)NR2iR2r, -OCH2CH2OR21, -NR2iS(0)2NR2rR2i” and - C(CH3)2OR2i; wherein R21, R21' and R2r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

4. Compound according to anyone of claims 1 to 3 wherein R7 is selected from substituted or unsubstituted aryl or substituted or unsubstituted aromatic heterocyclyl; preferably R7 is a substituted or unsubstituted group selected from phenyl, pyridinyl and thienyl.

5. Compound according to anyone of claims 1 to 4 wherein selected from

wherein

p is 0, 1 , 2, 3, 4 or 5;

q is 0, 1 , 2, 3, 4 or 5;

and Rz is as defined in the previous claims.

6. Compound according to anyone of claims 1 to 5 wherein X is a bond or a substituted or unsubstituted group selected from -CH2-, -CH2CH2- , C(O), - CH2C(0)-, -CH2CH2C(0)-, -NHC(0)CH2- and NHC(0)CH2CH2-;

7. Compound according to anyone of claims 1 to 6 wherein

p is 0, 1 , 2, 3, 4 or 5; preferably p is 0, 1 or 2.

8. Compound according to anyone of claims 1 to 7 wherein

q is 0, 1 , 2, 3, 4 or 5; preferably q is 1 or 2.

9. Compound according to any one of claims 1 to 8 wherein the compound is selected from

10. Compound according to any one of claims 1 to 8 wherein the compound is selected from

11. Process for the preparation of compounds of Formula (I) as defined in any one of claims 1 to 10

said process comprises one of step a) to k), a) wherein X represents a bond, and wherein Ri, R2, R3, R3', R4, R4·, Yi, Y2 and n have the meanings as defined in the description, said process comprises treating a compound of formula (lla),

wherein Q represents chloro, bromo, iodo or triflate, with a suitable reagent of formula (III-1)

RrH

HI-1 under standard Buchwald-Hartwig arylation conditions, or b) wherein -X- represents -[Chblp-, and wherein R1, R2, R3, R3', R4, R4·, Yi, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (lib) wherein r represents 0 to 4, with a reagent of formula (111-1)

R H

111-1 under standard reductive amination conditions, or c) wherein -X- represents -[CH2]P-, and wherein Ri, R2, R3, Ry, R4, R4 , Ui, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (lla),

wherein Q represents chloro, bromo, iodo or triflate, with an organometallic reagent of formula (MI-2)

wherein M represents a suitable organometallic group, preferably a boron or zinc reagent, and p has the meaning as defined in the description, or d) wherein -X- represents -[CH2]pC(0)[CH2]q- and q is 0, and wherein Ri, R2, R3, R3', R4, R4', YI , Y2, n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (lie)

with a reagent of formula (III-1)

R H

111-1 under conventional amidation conditions, or e) wherein -X- represents -[CH2]pN(Rz)C(0)[CH2]q-, and wherein Ri , R2, R3, R3 , R4, R4·, YI , Y2 , n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (VI)

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, p, q and Rz have the meanings as defined in the description, with a reagent of formula (III-1 ) R H

111-1 under conventional alkylation conditions, or f) wherein -X- represents -[CH2]pN(Rz)C(0)[CH2]q-, and wherein Ri, R2, R3, R3·, R4I R4', Yi, Y2, n, p and q have the meanings as defined in the description, said process comprises treating an amino compound of formula (lid)

wherein p and Rz have the meanings as defined in the description, with an acyl reagent of formula (III-3),

z

III-3 under amidation conditions, wherein Z represents OH or halogen and q has the meaning as defined in the description, or g) wherein -X- represents -[CH2]PN(Rz)C(0)[CH2]q-, p is 0, and wherein Ri, R2,

R3, R3', R4, R4', YI, Y2 , n, p and q have the meanings as defined in the description, said process comprises reacting a compound of formula (lla)

lla wherein Q represents chloro, bromo, iodo or triflate, with a carboxamido compound of formula (III-5)

under Ullmann or Buchwald-Hartwig arylation conditions, wherein q and Rz have the meanings as defined in the description, or h) wherein n is 0, and wherein Ri, R2, R3, R3', R4, R^, X, Y1 and Y2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alkylating agent of formula (VIII) wherein Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, or i) wherein n is 0, and wherein R1, R2, R3, R3', R4, R4·, X, Y1 and Y2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alcohol of formula (VIII), wherein Z represents OH, under conventional Mitsunobu conditions or j) wherein n is 0, and wherein Ri, R2, R3, R3', R4, R4·, X, Y1 and Y2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is halogen,

Vila with an alcohol of formula (VIII) in the presence of a strong base, wherein Z represents OH, or k) wherein n is 1 , and wherein R1, R2, R3, R3', R4, R4 , X, Y1 and Y2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vllb)

with an agent of formula (VIII), under standard alkylation reaction conditions, wherein either Z represents OH and G represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, or alternatively Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate and G represents

OH.

12. Use of a compound of Formula II, ll-LG, lla, lla-LG, lib, llb-LG, lie, llc-LG, lid, lld-LG, 111-1 , III-2, III-3, III-4, MI-5, IV, IVa, IVb, IVc, IVd, IVe, IVf, V, VI, VII, Vila, Vllb, VIII, VIII-LG or IX,

wherein Ri, R2, R3, R3', R4, R4·, X, Ui, Y2 , n, p, q, r and Rz have the meanings as defined in the description, Q represents chloro, bromo, iodo or triflate, LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, have the meanings as defined in the description, M represents a suitable organometallic group, Z represents OH or halogen, and G is OH, halogen or a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, for the preparation of compounds of Formula (I) as defined in any one of claims 1 to 10.

13. A pharmaceutical composition which comprises a compound of Formula (I) as defined in any one of claims 1 to 10 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.

14. A compound of Formula (I) as defined in any one of claims 1 to 10 for use as a medicament. 15. A compound of Formula (I) as defined in any one of claims 1 to 10 for use as a medicament; preferably for use as a medicament for the treatment of pain, especially medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia.

Description:
DIALKYLAMINOARYLPIPERIDINYL-O-PHENOXY AND O- BENZYLOXYPROPYLAMINO DERIVATIVES HAVING MULTIMODAL ACTIVITY AGAINST PAIN

FIELD OF THE INVENTION

The present invention relates to compounds having dual pharmacological activity towards both the a 2 d subunit of the voitage-gated caicium channel, and the m-opioid receptor (MOR or mu-opioid receptor) and more particularly to dialkylaminoarylpiperidinyl-o-phenoxy and o-benzyloxypropylamino derivatives having this pharmacological activity, to processes of preparation of such compounds, to pharmaceutical compositions comprising them, and to their use in therapy, in particular for the treatment of pain.

BACKGROUND OF THE INVENTION

The adequate management of pain constitutes an important challenge, since currently available treatments provide in many cases only modest improvements, leaving many patients unrelieved (Turk, D.C., Wilson, H.D., Cahana, A.; 201 1 ; Lancet, 377; 2226- 2235). Pain affects a big portion of the population with an estimated prevalence of 20 % and its incidence, particularly in the case of chronic pain, is increasing due to the population ageing. Additionally, pain is clearly related to comorbidities, such as depression, anxiety and insomnia, which leads to important productivity losses and socio-economical burden (Goldberg, D.S., McGee, S.J.; 201 1 ; BMC Public Health·, 1 1 ; 770). Existing pain therapies include non-steroidal anti-inflammatory drugs (NSAIDs), opioid agonists, calcium channel blockers and antidepressants, but they are much less than optimal regarding their safety ratio. All of them show limited efficacy and a range of secondary effects that preclude their use, especially in chronic settings.

Voltage-gated calcium channels (VGCC) are required for many key functions in the body. Different subtypes of voltage-gated calcium channels have been described (Zamponi et al., Pharmacol Rev. 2015 67:821-70). The VGCC are assembled through interactions of different subunits, namely on (Ca v ai), b (Ca v ) a 2 d (Ca v a 2 6) and g (Ca v y). The on subunits are the key porous forming units of the channel complex, being responsible for the Ca 2+ conduction and generation of Ca 2+ influx. The a 2 d, b, and g subunits are auxiliary, although very important for the regulation of the channel, since they increase the expression of the oci subunits in the plasma membrane as well as modulate their function, resulting in functional diversity in different cell types. Based on their physiological and pharmacological properties, VGCC can be subdivided into low voltage-activated T-type (Ca v 3.1 , Ca v 3.2, and Ca v 3.3), and high voltage-activated L- (Ca v 1.1 through Ca v 1.4), N-(Ca v 2.2), P/Q-(Ca v 2.1 ), and R-(Ca v 2.3) types, depending on the channel forming Cava subunits. All of these five subclasses are found in the central and peripheral nervous systems. Regulation of intracellular calcium through activation of these VGCC plays obligatory roles in: 1 ) neurotransmitter release, 2) membrane depolarization and hyperpolarization, 3) enzyme activation and inactivation, and 4) gene regulation (Perret and Luo, Neurotherapeutics. 2009 6:679-92; Zamponi et al., 2015 supra ; Neumaier et al., Prog Neurobiol. 2015 129: 1-36.). A large body of data has clearly indicated that VGCC are implicated in mediating various disease states including pain processing. Drugs interacting with the different calcium channel subtypes and subunits have been developed. Current therapeutic agents include drugs targeting L-type Ca v 1.2 calcium channels, particularly 1 ,4-dihydropyridines, which are widely used in the treatment of hypertension. T-type (Ca v 3) channels are the target of ethosuximide, widely used in absence epilepsy. Ziconotide, a peptide blocker of N-type (Ca v 2.2) calcium channels, has been approved as a treatment of intractable pain. (Perret and Luo, 2009, supra\ Vink and Alewood, Br J Pharmacol. 2012 167:970-89.).

The Ca v 1 and Ca v 2 subfamilies contain an auxiliary a 2 d subunit, which is the therapeutic target of the gabapentinoid drugs of value in certain epilepsies and chronic neuropathic pain. To date, there are four known a 2 d subunits, each encoded by a unique gene and all possessing splice variants. Each a 2 d protein is encoded by a single messenger RNA and is post-translationally cleaved and then linked by disulfide bonds. Four genes encoding a 2 d subunits have now been cloned. a 2 d-1 was initially cloned from skeletal muscle and shows a fairly ubiquitous distribution. The a 2 d-2 and a 2 d-3 subunits were subsequently cloned from brain. The most recently identified subunit, a 2 d-4, is largely non-neuronal. The human a 2 d-4 protein sequence shares 30, 32 and 61 % identity with the human a 2 d-1 , a 2 d-2 and a 2 d-3 subunits, respectively. The gene structure of all a 2 d subunits is similar. All a 2 d subunits show several splice variants (Davies et al., Trends Pharmacol Sci. 2007 28:220-8.; Dolphin AC, Nat Rev Neurosci. 2012 13:542-55., Biochim Biophys Acta. 2013 1828:1541-9.). The Ca v a25-1 subunit may play an important role in neuropathic pain development (Perret and Luo, 2009, supra Vink and Alewood, 2012, supra). Biochemical data have indicated a significant Ca v ct26-1 , but not Ca v oi28-2, subunit upregulation in the spinal dorsal horn, and DRG (dorsal root ganglia) after nerve injury that correlates with neuropathic pain development. In addition, blocking axonal transport of injury-induced DRG Ca v oi25-1 subunit to the central presynaptic terminals diminishes tactile allodynia in nerve injured animals, suggesting that elevated DRG Ca v a25-1 subunit contributes to neuropathic allodynia.

The Ca v a 2 5-1 subunit (and the Ca v a 2 6-2, but not Ca v a 2 6-3 and Ca v a 2 5-4, subunits) is the binding site for gabapentin which has anti-allodynic/ hyperalgesic properties in patients and animal models. Because injury-induced Ca v a28-1 expression correlates with neuropathic pain development and maintenance, and various calcium channels are known to contribute to spinal synaptic neurotransmission and DRG neuron excitability, injury-induced Ca v cx25-1 subunit upregulation may contribute to the initiation and maintenance of neuropathic pain by altering the properties and/or distribution of VGCC in the subpopulation of DRG neurons and their central terminals, therefore modulating excitability and/or synaptic neuroplasticity in the dorsal horn. Intrathecal antisense oligonucleotides against the Ca v( X25-1 subunit can block nerve injury-induced Ca v a 2 5-1 upregulation and prevent the onset of allodynia and reserve established allodynia.

As mentioned above, the a å d subunits of VGCC form the binding site for gabapentin and pregabalin, which are structural derivatives of the inhibitory neurotransmitter GABA although they do not bind to GABAA, GABAB, or benzodiazepine receptors, or alter GABA regulation in animal brain preparations. The binding of gabapentin and pregabalin to the Ca v oi28 subunit results in a reduction in the calcium-dependent release of multiple neurotransmitters, leading to efficacy and tolerability for neuropathic pain management. Gabapentinoids may also reduce excitability by inhibiting synaptogenesis (Perret and Luo, 2009, supra ; Vink and Alewood, 2012, supra, Zamponi et al., 2015, supra).

As mentioned before, there are few available therapeutic classes for the treatment of pain, and opioids are among the most effective, especially when addressing severe pain states. They act through three different types of opioid receptors (mu, kappa and gamma) which are transmembrane G-protein coupled receptors (GPCRs). Still, the main analgesic action is attributed to the activation of the m-opioid receptor (MOR). However, the general administration of MOR agonists is limited due to their important side effects, such as constipation, respiratory depression, tolerance, emesis and physical dependence [Meldrum, M.L. (Ed.)· Opioids and Pain Relief: A Historical Perspective. Progress in Pain Research and Management, Vol 25. IASP Press, Seattle, 2003] Additionally, MOR agonists are not optimal for the treatment of chronic pain as indicated by the diminished effectiveness of morphine against chronic pain conditions. This is especially proven for the chronic pain conditions of neuropathic or inflammatory origin, in comparison to its high potency against acute pain. The finding that chronic pain can lead to MOR down-regulation may offer a molecular basis for the relative lack of efficacy of morphine in long-term treatment settings [Dickenson, A.H., Suzuki, R. Opioids in neuropathic pain: Clues from animal studies. Eur J Pain 9, 1 13-6 (2005)]. Moreover, prolonged treatment with morphine may result in tolerance to its analgesic effects, most likely due to treatment-induced MOR down-regulation, internalization and other regulatory mechanisms. As a consequence, long-term treatment can result in substantial increases in dosing in order to maintain a clinically satisfactory pain relief, but the narrow therapeutic window of MOR agonists finally results in unacceptable side effects and poor patient compliance.

Polypharmacology is a phenomenon in which a drug binds multiple rather than a single target with significant affinity. The effect of polypharmacology on therapy can be positive (effective therapy) and/or negative (side effects). Positive and/or negative effects can be caused by binding to the same or different subsets of targets; binding to some targets may have no effect. Multi-component drugs or multi-targeting drugs can overcome toxicity and other side effects associated with high doses of single drugs by countering biological compensation, allowing reduced dosage of each compound or accessing context-specific multitarget mechanisms. Because multitarget mechanisms require their targets to be available for coordinated action, one would expect synergies to occur in a narrower range of cellular phenotypes given differential expression of the drug targets than would the activities of single agents. In fact, it has been experimentally demonstrated that synergistic drug combinations are generally more specific to particular cellular contexts than are single agent activities, such selectivity is achieved through differential expression of the drugs’ targets in cell types associated with therapeutic, but not toxic, effects (Lehar et al., Nat Biotechnol 2009; 27: 659-666.). In the case of chronic pain, which is a multifactorial disease, multi-targeting drugs may produce concerted pharmacological intervention of multiple targets and signaling pathways that drive pain. Because they actually make use of biological complexity, multi-targeting (or multi-component drugs) approaches are among the most promising avenues toward treating multifactorial diseases such as pain (Gilron et al., Lancet Neurol. 2013 Nov; 12(11 ): 1084-95.). In fact, positive synergistic interaction for several compounds, including analgesics, has been described (Schroder et al., J Pharmacol Exp Ther. 201 1 ; 337:312-20. Erratum in: J Pharmacol Exp Ther. 2012; 342:232.; Zhang et al., Cell Death Dis. 2014; 5:e1 138.; Gilron et al., 2013, supra).

Given the significant differences in pharmacokinetics, metabolisms and bioavailability, reformulation of drug combinations (multi-component drugs) is challenging. Further, two drugs that are generally safe when dosed individually cannot be assumed to be safe in combination. In addition to the possibility of adverse drug-drug interactions, if the theory of network pharmacology indicates that an effect on phenotype may derive from hitting multiple targets, then that combined phenotypic perturbation may be efficacious or deleterious. The major challenge to both drug combination strategies is the regulatory requirement for each individual drug to be shown to be safe as an individual agent and in combination (Hopkins, Nat Chem Biol. 2008; 4:682-90.).

An alternative strategy for multitarget therapy is to design a single compound with selective polypharmacology (multi-targeting drug). It has been shown that many approved drugs act on multiple targets. Dosing with a single compound may have advantages over a drug combination in terms of equitable pharmacokinetics and biodistribution. Indeed, troughs in drug exposure due to incompatible pharmacokinetics between components of a combination therapy may create a low-dose window of opportunity where a reduced selection pressure can lead to drug resistance. In terms of drug registration, approval of a single compound acting on multiple targets faces significantly lower regulatory barriers than approval of a combination of new drugs (Hopkins, 2008, supra).

Thus, the present application, relates to the advantages of having dual activity, for m- receptor and the a 2 d-1 subunit of voltage-gated calcium channels, in the same molecule to treat chronic pain. In this way, the present invention relates to compounds having a complementary dual mechanism of action (m-receptor agonist and blocker of the a 2 d subunit, in particular the a 2 d-1 subunit, of voltage-gated calcium channels) which implies a better profile of tolerability than the strong opioids (morphine, oxycodone, fentanyl etc) and/or better efficacy and tolerability than gabapentinoids (pregabalin and gabapentin).

Pain is multimodal in nature, since in nearly all pain states several mediators, signaling pathways and molecular mechanisms are implicated. Consequently, monomodal therapies fail to provide complete pain relief. Currently, combining existing therapies is a common clinical practice and many efforts are directed to assess the best combination of available drugs in clinical studies (Mao, J., Gold, M.S., Backonja, M.; 2011 ; J. Pain; 12; 157-166).

Accordingly, there is still a need to find compounds that have an alternative or improved pharmacological activity in the treatment of pain, being both effective and showing the desired selectivity, and having good“drugability” properties, i.e. good pharmaceutical properties related to administration, distribution, metabolism and excretion.

The authors of the present invention, have found a serie of compounds that show dual pharmacological activity towards both the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel, and the m-opioid receptor (MOR or mu-opioid receptor) resulting in an innovative, effective and alternative solution for the treatment of pain.

In view of the existing results of the currently available therapies and clinical practices, the present invention offers a solution by combining in a single compound binding to two different targets relevant for the treatment of pain. This was mainly achieved by providing the compounds according to the invention that bind both to the m-opioid receptor and to the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel.

SUMMARY OF THE INVENTION

In this invention a family of structurally distinct dialkylaminoarylpiperidinyl-o-phenoxy and o-benzyloxypropylamino derivatives, encompassed by formula (I), which have a dual pharmacological activity towards both the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel, and the m-opioid receptor was identified thus solving the above problem of identifying alternative or improved pain treatments by offering such dual compounds. The main object of the invention is directed to a compound having a dual activity binding to the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor for use in the treatment of pain.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as dual ligands of the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor it is a very preferred embodiment if the compound has a binding expressed as K, responding to the following scales:

Ki(p) is preferably < 1000 nM, more preferably < 500 nM, even more preferably < 100 nM.

K,(a 2 d-1 ) is preferably < 10000 nM, more preferably < 5000 nM, even more preferably

< 500 nM or even more preferably < 100 nM.

The invention is directed in a main aspect to a compound of general Formula (I),

wherein Ri, R 2 , R 3 , R 3 ·, R 4 , R 4' , X, Ui, Y 2 and n are as defined below in the detailed description.

A further object of the invention refers to the processes for preparation of compounds of general formula (I). A still further object of the invention refers to the use of intermediate compounds for the preparation of a compound of general formula (I).

It is also an object of the invention a pharmaceutical composition comprising a compound of formula (I).

Finally, it is an object of the invention the use of compound as a medicament and more particularly for the treatment of pain and pain related conditions.

DETAILED DESCRIPTION OF THE INVENTION

In this invention a family of structurally distinct dialkylaminoarylpiperidinyl-o-phenoxy and o-benzyloxypropylamino derivatives, encompassed by formula (I), which have a dual pharmacological activity towards both the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel, and the m-opioid receptor was identified, thus solving the above problem of identifying alternative or improved pain treatments by offering such dual compounds.

The main object of the invention is directed to a compound having a dual activity binding to the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor, for use in the treatment of pain.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as dual ligands of the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor, it is a very preferred embodiment if the compound has a binding expressed as K, responding to the following scales:

Ki(p) is preferably < 1000 nM, more preferably < 500 nM, even more preferably < 100 nM.

K ί (a 2 d-1) is preferably < 10000 nM, more preferably < 5000 nM, even more preferably < 500 nM or even more preferably < 100 nM.

The applicant has surprisingly found that the problem of providing a new effective and alternative for treating pain and pain related disorders can be solved by using a multimodal balanced analgesic approach combining two different synergistic activities in a single drug (i.e., dual ligands which are bifunctional and bind to m-opioid receptor and to a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel), thereby enhancing through the a 2 d blockade without increasing the undesirable side effects. This supports the therapeutic value of a dual agent, whereby the a 2 d binding component acts as an intrinsic adjuvant of the MOR binding component.

A dual compound that possess binding to both the m-opioid receptor and to the 2 d subunit of the voltage-gated calcium channel shows a highly valuable therapeutic potential by achieving an outstanding analgesia (enhanced in respect to the potency of the opioid component alone) with a reduced side-effect profile (safety margin increased compared to that of the opioid component alone) versus existing opioid therapies.

Advantageously, the dual compounds according to the present invention would in addition show one or more the following functionalities: blockade of the a 2 d subunit, in particular the a 2 d-1 subunit, of the voltage-gated calcium channel and m-opioid receptor agonism

It has to be noted, though, that functionalities“antagonism” and“agonism” are also sub- divided in their effect into subfunctionalities like partial agonism or inverse agonism. Accordingly, the functionalities of the compound should be considered within a relatively broad bandwidth.

An antagonist blocks or dampens agonist-mediated responses. Known subfunctionalities are neutral antagonists or inverse agonists.

An agonist increases the activity of the receptor above its basal level. Known subfunctionalities are full agonists, or partial agonists.

In addition, the two mechanisms complement each other since MOR agonists are only marginally effective in the treatment of neuropathic pain, while the blockers of the a 2 d subunit, in particular the a 2 d-1 subunit, of voltage-gated calcium channels show outstanding effects in preclinical neuropathic pain models. Thus, the a 2 d component, in particular the a 2 d-1 component, adds unique analgesic actions in opioid-resistant pain. Finally, the dual approach has clear advantages over MOR agonists in the treatment of chronic pain as lower and better tolerated doses would be needed based on the potentiation of analgesia but not of the adverse events of MOR agonists. A further advantage of using designed multiple ligands is a lower risk of drug-drug interactions compared to cocktails or multi-component drugs, thus involving simpler pharmacokinetics and less variability among patients. Additionally, this approach may improve patient compliance and broaden the therapeutic application in relation to monomechanistic drugs, by addressing more complex aetiologies. It is also seen as a way of improving the R&D output obtained using the“one drug-one target” approach, which has been questioned over the last years [Bornot A, Bauer U, Brown A, Firth M, Hellawell C, Engkvist O. Systematic Exploration of Dual-Acting Modulators from a Combined Medicinal Chemistry and Biology Perspective. J. Med. Chem, 56, 1 197-1210 (2013)].

In its broader aspect, the present invention is directed to compounds of general Formula (I):

wherein

X is selected from a bond, -[C(R a R b )]p-, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ]pN(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ]q-;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2- e alkynyl; R b is selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 .e alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(RioRio )-; wherein R10 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl; alternatively, R10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y 2 is— C(Rio "Rio ) _ i wherein R10 " and R10- are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R10 · and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is O, 1 , 2, 3, 4 or 5;

Rs, Rs·, Rs- and R 5” are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R5 and Rs· and/or R 5 and Rs - taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

R6, R6', R6” and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2.6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 6 and R 6 - and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and Re· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Re is selected from substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re- is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and Rs· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl,

R 3 is selected from substituted or unsubstituted C 1 -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; R 3' is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 4 and R 4 · are independently selected from halogen, -R 4I , -OR 4I , -NO2, -NR 4i R 4 r, - NR 4i C(0)R r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R 4r , -NR 4i C(0)NR 4 rR 4 r, -SR 41 , -S(0)R i , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R 4 r, -OCH 2 CH 2 OR I , -

NR 4i S(0) 2 NR 4r R 4 r and -C(CH 3 ) 2 OR I ; wherein R 4 I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

These compounds according to the invention are optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a particular embodiment, if X is selected from -[CH 2 ]pC(0)N(R z )[CH 2 ] q -, and - [CH 2 ] p N(Rz)[CH 2 ]q-, q is 1 , 2, 3, 4 or 5.

In another particular embodiment if X is selected from a bond, -[C(R a R b )] P -, - [CH 2 ] p C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )C(0)[CH 2 ] q -, q is 0, 1 , 2, 3, 4 or 5; and if X is selected from -[CH 2 ] p C(0)N(R z )[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -, q is 1 , 2, 3, 4 or 5.

In another embodiment, these compounds according to the invention are optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof.

In a further embodiment the compound according to the invention is a compound of general Formula (I)

wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH2] P C(0)N(R z )[CH 2 ]q-, - [CH 2 ] P N(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted C alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 .e alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-e alkyl; p is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(RioR-io')-; wherein Rio and Ri 0 are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2- e alkynyl; alternatively, R 10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y2 is -C(Rio"Rio ) i wherein R 10 · and Rio- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 -e alkynyl; alternatively, R 10” and RKT may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R5, Rs·, Rs and R5- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 5 and Rs and/or R 5 and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs -, if substituted, is substituted with one or more substituent/s selected from -OR51, halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R5-R5' and/or R5-R5-, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -N0 2 , -NRsiRsr, -NR 5i C(0)R 5 r, -NR 5i S(0) 2 Rsr, -S(0) 2 NR 5i R 5 r, - NR 5i C(0)NR 5 rR 5 r, -SR51 , -S(0)Rsi, -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0Rsi, -C(0)NRsiRsr, -OCH 2 CH 2 OR5i, NR 5i S(0) 2 NR 5i' R5r and -C(CH 3 ) 2 OR 5 I;

wherein R 51 , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 .e alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

Re, Re , Re- and R 6 - are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, Re and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , R 6’ R 6 - and Re-, if substituted, is substituted with one or more substituent/s selected from -ORei , halogen, - CN, haloalkyl, haloalkoxy and -NReiRer;

wherein the cycloalkyl, as defined in R 6 -R 6 · and/or R 6 -R 6 -, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R61 , -OR61, -NO2, -NR61R6I’, -NReiC(0)Rer, -NR6iS(0)2R6r, -S(0)2NR6iR6i’, - NR6iC(0)NRerRer, -SRei , -S(0)Rei , -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -OCH2CH2OR61 ,

NR6iS(0)2N wherein Rei , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R I , -OR 7I , -NO2, - NR 7i R 7r , -NR 7I C(0)R 7V , -NR 7i S(0) 2 R r, -S(0) 2 NR 7i R 7r ,

NR 7i C(0)NR 7 rR 7i " , -SR 7I , -S(0)R 71 , -S(0) 2 R I , -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR 7I R 7I , -OCH2CH 2 OR 7I , NR 7i S(0) 2 NR 7 rR 7i" and -C(CH 3 ) 2 OR 7I ; wherein R I , R r and R 7 r· are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; Re is selected from substituted or unsubstituted Cve alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in Re, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, -CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl defined in Re, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -ORei, -NO2, -NReiRer, -NReiC(0)Rer, -NReiS(0)2Rer, -S(0)2NReiRer, - NReiC(0)NRei Rer, -SRei , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NR 8i Rer, -0CH 2 CH20Rei, NReiS(0)2NRerRei” and -C(CH3)20Rei; wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

Re· is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in R 8 \ if substituted, is substituted with one or more substituent/s selected from -OR 8 2, halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R 82' ; the cyclolakyl defined in R 8 ·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 2,

-OR 82 , -NO2, -NR 8 2R 8 2', -NR 82 C(0)R 82' , -NR 82 S(0) 2 R82', -S(0) 2 NR 82 R 82 ·, - NR 82 U(0)NR 82' K 82” , -SR 82 , -S(0)R 82 , -S(0) 2 R 82 , — CN, haloalkyl, haloalkoxy, -C(0)0R 82 , -C(0)NR 82 R 82 ·, -0CH2CH20R 82 ,

NR 82 S(0)2NR 82' R 82' and -C(CH3)20R 82 ; wherein R 8 2, R 8 2· and R 82" are independently selected from hydrogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

alternatively, R 8 and R 8 · taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in R 8 -R 8 ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 83 , -OR 83 , - NO2, -NR 83 R 83' , -NR 83 C(0)R 83’ , -NR 83 S(0) 2 R 83' , -S(0) 2 NR 83 R 83' ,

NR 83 C(0)NR 83' R 83" , -SR 83 , -S(0)RS3, -S(0) 2 RS3, -CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R 83 ·, -0CH 2 CH20R 83 ,

NR 83 S(0)2NR 83' R 83" and -C(CH3)20R 83 ; wherein R 83 , R 8 3· and R 83" are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl;

R2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen, -R21 , -OR21 , -NO2, -NR21R21', -NR 2i C(0)R2r, -NR2iS(0)2R2i’, -S(0)2NR2iR2r, - NR 2i C(0)NR 2 rR2r, -SR21 , -S(0)R 2 I , -S(0) 2 R 2 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 21 , - C(0)NR 2i R 2 r, -OCH2CH2OR21, -NR2iS(0) 2 NR 2 rR 2 r and -C(CH 3 ) 2 OR2i; wherein R21, R21· and R 2 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R3 is selected from substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 3 I , halogen, -CN, haloalkyl, haloalkoxy and -NR 3i R 3r ; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 3I , -OR 3I , -NO2, -NR 3i R 3 r, -NR 3i C(0)R 3 r, -NR 3i S(0)2R3r, -S(0) 2 NR 3i R 3 r, - NR 3i C(0)NR 3r R 3 r, -SR 3I , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)0R 3i , -C(0)NR 3i R 3r , -OCH 2 CH 2 OR 3I , NR 3i S(0) 2 NR 3 rR 3 r and -C(CH 3 ) 2 OR 3 I ;

wherein R 3I , R 3r and R 3 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted C-i-b alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2 -e alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3' , if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R 32 and R 32' are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R 4I , -OR 4I , -NO2, -NR 4i R r, - NR 4i C(0)R 4 , -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 41 R 4 r, -NR 41 C(0)NR 4 rR 4 r, -SR 4I , -S(0)R 41 , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4I , -C(0)NR 4i R 4 , -OCH 2 CH 2 OR 4I , -

NR 4i S(0) 2 NR 4i' R 4 r and -C(CH 3 ) 2 0R 4I ; wherein R 4I , R 4 r and R 4i - are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR 13 , halogen, -CN, haloalkyl, haloalkoxy and -NR 13 R 13' ; wherein R 13 and R 13' are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -R I4 , -ORu, -NO 2 , -NR I4 R I4 ·, - NR I4 C(0)R I ' , -NR I4 S(0) 2 R I ·, -S(0) 2 NR 14 R 14' , - NR I4 C(0)NR I4' R I4 " , -SR I4 , -S(0)Ri 4 , - S(0) 2 Ri4, -CN, haloalkyl, haloalkoxy, -C(0)ORM, -C(0)NRi 4 Ri4·, -OCH 2 CH 2 ORi4, - NRi 4 S(0) 2 NRi4-Ri4" and -C(CH3) 2 ORi4;

wherein R M , R^ and R^- are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyc!y!;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention is a compound of general Formula (I)

wherein

X is selected from a bond, -[C(R a R b )] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ]pN(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -; R a is selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2- 6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; if X is selected from a bond, -[C(R a Rb)] P -, -[CH 2 ]pC(0)[CH2]q- and -

[CH 2 ]pN(Rz)C(0)[CH 2 ] q -, q is 0, 1 , 2, 3, 4 or 5; and if X is selected from -[CH 2 ]pC(0)N(Rz)[CH 2 ]q- and -[CH 2 ]pN(Rz)[CH 2 ]q-, q is 1 , 2, 3, 4 or 5; p is O, 1 , 2, 3, 4 or 5; n is 0 or 1 ;

Yi is -C(RioRio )-; wherein R 10 and Ri 0 are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y2 is— C(Rio "Rio ) ! wherein Rio- and Rio- are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rio- and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs·, Rs- and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 5 and R 5 · and/or Rs · and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs Rs- and Rs ', if substituted, is substituted with one or more substituent/s selected from -OR51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R5-R5' and/or Rs -Rs ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -NO2, -NRsiRsr, -NRsiC(0)Rsr, -NR5iS(0) 2 Rsr, -S(0) 2 NR5iR 5 r, - NR 5i C(0)NR 5 rR 5 r, -SR51 , -S(0)R 5i , -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0R 5i , -C(0)NR 5i R 5 r, -OCH 2 CH 2 OR 5 I ,

NR5iS(0) 2 NR5i’R5r and -C(CH3) 2 ORSI ;

wherein R51, Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2- 6 alkenyl, and substituted or unsubstituted C 2- 6 alkynyl;

Re, Re·, Re·· and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl; alternatively, Re and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and Re· and/or Re- and Re · taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re- and Re ·, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, - CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl, as defined in R 6 -R 6 · and/or R 6 - 6-', if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -OR61, -N0 2 , -NR61R6I’, -NReiC(0)Rei·, -NReiS(0) 2 Rev, -S(0) 2 NReiRei’ - NR6iC(0)NRerRer, -SRei , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NR 6i R 6 r, -OCH 2 CH 2 ORei,

NReiS(0) 2 NRerRei" and -C(CH3) 2 OR6i; wherein R61, Rer and R 6 r are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2- e alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 7I , -OR 7I , -NO2, - NR 7i R 7 , -NR 7i C(0)R 7 r, -NR 7i S(0) 2 R 7 r, -S(0) 2 NR 71 R 7r ,

NR 71 C(0)NR 7r R 7i ' , -SR 7I , -S(0)R i , -S(0) 2 R 7i , -CN, haloalkyl, haloalkoxy, -C(0)0R i , -C(0)NR 7i R 7r , -OCH 2 CH 2 OR I ,

NR i S(0) 2 NR 7 R 7r and -C(CH 3 ) 2 OR 7I ; wherein R I , R r and R 7 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2- e alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

Rs is selected from substituted or unsubstituted C alkyl, substituted or unsubstituted C 2- e alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -ORsi, halogen, -CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl defined in Re, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rsi, -ORsi, -NO2, -NReiRer, -NR8iC(0)Rer, -NR8iS(0)2R8r, -S(0)2NR8iRer, - NR 8i C(0)NR 8 rR 8i” , -SR 8i , -S(0)R8i, -S(0) 2 R8i, — CN, haloalkyl, haloalkoxy, -C(0)0Rei , -C(0)NR 8i Rer, -OCH2CH2OR81,

NReiS(0)2NR 8 rRer and -C(CH3)20R8i; wherein Rei, Rsr and Rer are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C2-6 alkynyl;

Re· is selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in Re \ if substituted, is substituted with one or more substituent/s selected from -ORs2, halogen, -CN, haloalkyl, haloalkoxy and -NR82R82'; the cyclolakyl defined in R 8 ·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rs 2 , -OR82, -NO2, -NR82R82’, -NR82C(0)R82’, -NR82S(0)2Re2', -S(0)2NRe2R82’, - NR8 2 C(0)NR82'R82” -SRe2 , -S(0)Rs2, _ S(0)2R82, - CN, haloalkyl, haloalkoxy, -C(0)0Re2, -C(0)NRe2R82·, -OCH2CH2OR82,

NR82S(0)2NR82’R82” and -C(CH3)20R82; wherein Re 2 , Re 2' and Re 2 ·· are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

alternatively, R 8 and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in Re-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Re3, -ORe3, - NO2, -NRe3R83', -NRe3C(0)Re3’, -NRe3S(0)2Rs3’, -S(0)2NRe3Re3',

NR 83 C(0)NR83'R83", -SR83 , -S(0)R83, _ S(0)2R83, — CN, haloalkyl, haloalkoxy, -C(0)ORe3, -C(0)NRe3R83·, -OCH2CH2OR83,

NR83S(0)2NR83'R83” and -C(CH 3 )20R 83 ; wherein R 8 3, Rs3· and R 8 3" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, wherein the aryl or heterocyclyl in R2, if substituted, is substituted with one or more substituent/s selected from halogen, -R21, -OR21, -NO2, -NR21R21', -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R2r, -S(0) 2 NR2iR 2 r, - NR 2i C(0)NR 2 rR2r, -SR21 , -S(0)R 21 , -S(0) 2 R 2i , -CN, haloalkyl, haloalkoxy, -C(0)0R2i, - C(0)NR 2i R 2 r, -OCH2CH2OR21, -NR 21 S(0) 2 NR 21 R21” and -C(CH 3 )20R 2I ; wherein R21, R å r and R 2 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; R 3 is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R3, if substituted, is substituted with one or more substituent/s selected from -OR31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31 R31'; wherein the cycloalkyl in R 3 , also in _alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 31 , -OR31, -NO2, -NR31R31’, -NR 3i C(0)R 3 r, -NR3iS(0)2R3 , -S(0)2NR3iR3r, - NR31C(0)NR 31' R31", -SR31 , -S(0)R 31 , -S(0) 2 R 31 , -CN, haloalkyl, haloalkoxy, -C(0)0R 3i , -C(0)NR 3i R 3 r, -OCH2CH2OR31,

NR 3i S(0) 2 NR 3 rR3r and -C(CH3)20R3i ;

wherein R31 , R31· and R31” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3' , if substituted, is substituted with one or more substituent/s selected from -OR32, halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R32 and R32' are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; R 4 and R 4' are independently selected from halogen, -R41, -OR41, -NO2, -NR41R41', - NR 4i C(0)R 4 r, -NR4iS(0) 2 R4r, -S(0) 2 NR4iR 4i ·, -NR 4i C(0)NR 4 rR4r, -SR41 , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR 4 I R 4 I , -OCH2CH2OR41, - NR 4i S(0) 2 NR4rR4i” and -C(CH 3 ) 2 OR4i; wherein R 41 , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR13, halogen, -CN, haloalkyl, haloalkoxy and -NRi3Ri3·; wherein R13 and R13' are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2 -e alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -R14, -OR14, -NO2, -NR14R14 , - NRi 4 C(0)Ri4·, -NRi 4 S(0) 2 Ri4·, -S(0) 2 NRi 4 Ri4·, - NRi 4 C(0)NRi4'Ri4", -SRH , -S(0)Ri 4 , - S(0) 2 Ri 4 , -CN, haloalkyl, haloalkoxy, -C(0)0Ri 4 , -C(0)NRi 4 Ri4·, -OCH2CH2OR14, - NRI 4 S(0)2NRI4'RI4·' and -C(CH 3 )20RI 4 ;

wherein R 14 , Ri 4 and Ru- are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2 -e alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I )

wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, X and n are as defined in the detailed description, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I )

(0 wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH2] P C(0)[CH2] q -, -[CH2] P C(0)N(R z )[CH2] q -, - [CH 2 ] P N(Rz)C(0)[CH 2 ] q - and -[CH 2 ] P N(Rz)[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R 5 , Rs·, Rs- and R 5 are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R5 and Rs· and/or Rs- and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

Re, Re·, Re- and R^ are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R6 and Re· and/or Re- and Re · taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R6 and R6· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Re is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 -6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re· is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and Retaken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl,

R 3 is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

R 3' is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R41, -OR41, -NO2, -NR41R41 , - NR 4i C(0)R 4 r, -NR4iS(0) 2 R 4 r, -S(0) 2 NR 4i R4r, -NR4iC(0)NR 4 rR 4 r, -SR41 , -S(0)R 41 , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR 4 IR 4 I , -OCH2CH2OR41, - NR4iS(0) 2 NR4i'R4r and -C(CH 3 ) 2 OR 4 I; wherein R 41 , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I )

O’) wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH2] P C(0)[CH 2 ]q-, -[CH 2 ]pC(0)N(Rz)[CH 2 ] q -, - [CH 2 ]pN(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R 2 )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R P is selected from hydrogen, halogen, substituted or unsubstituted C 6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2- e alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-6 alkyl;

P is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs\ R5” and R5- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2 -6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rs and Rs· and/or Rs- and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs -, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R 5 -R 5' and/or Rs -Rs , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 51 , -OR51, -NO2, -NR51R51', -NR 5i C(0)R 5 r, -NR 5I S(0) 2 R5V, -S(0) 2 NRsiRsr, - NR 5i C(0)NR 5 rR 5 r, -SR51 , -S(0)R 5i , -S(0) 2 R 5i , -CN; haloalkyl, haloalkoxy, -C(0)0R 5i , -C(0)NR 5i Rsi', -OCH2CH2OR51, NR5iS(0)2NR5rR5i” and -C(CH3)20R5i;

wherein R51, Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 6 and Re' and/or Re- and Re taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and Re· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re- and R 6 -, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, - CN, haloalkyl, haloalkoxy and -NReiRer;

wherein the cycloalkyl, as defined in F Re· and/or Re-Re-, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R61, -ORei, -NO2, -NReiRer, -NR 6i C(0)R 6 r, -NR 6i S(0) 2 R6r, -S(0) 2 NReiRer, - NR 6i C(0)NR 6 rR 6i" , -SR 6I , -S(0)R 6i , -S(0) 2 R 6i , -CN, haloalkyl, haloalkoxy, -C(0)0R6i, -C(0)NR6iR6r, -OCH 2 CH 2 OR6i,

NR 6i S(0) 2 NR6i R 6 r and -C(CH3) 2 OR6i ; wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl, and substituted or unsubstituted C 2- e alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 7i , -OR 7I , -N0 2 , - NR 7i R 7r , -NR 7I C(0)R TT , -NR 7i S(0) 2 R r, -S(0) 2 NR 71 R 7r ,

NR 7i C(0)NR 7r R 7i , -SR 7I , -S(0)R 7i , -S(0) 2 R 7i , -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR 7i R 7r , -OCH 2 CH 2 OR I ,

NR 7i S(0) 2 NR 71 R 7 r and -C(CH 3 ) 2 OR 7I ; wherein R 7I , R 7 r and R 7 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2- e alkynyl; R 8 is selected from substituted or unsubstituted Ci- 8 alkyl, substituted or unsubstituted C 2-8 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -OR 8 I , halogen, -CN, haloalkyl, haloalkoxy and -NR 8 I R 8 I·; wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 I , -OR 8 I , -NO2, -NR 8i R 8 r, -NR 8i C(0)R 8 r, -NR 8i S(0)2R 8i' , -S(0)2NR 8i R 8 r, - NR 8 IC(0)NR 8 I R 8 I ", -SRei , -S(0)Rei, -S(0) 2 R 8i , -CN, haloalkyl, haloalkoxy, -C(0)0R 8i , -C(0)NR 8i R 8 r, -OChhCh^ORsi,

NR 8i S(0)2NR 8 rR 8 r and -C(CH 3 ) 2 0R 8i ;

wherein R 8 I , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Ci. 8 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

Re· is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in Re·, if substituted, is substituted with one or more substituent/s selected from -ORs 2 , halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R82·; the cyclolakyl defined in R 8 ·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Re2, -OR82, -NO2, -NR 82 R82', -NRe2C(0)R82·, -NRe2S(0)2R82’, -S(0)2NR82R82’, - NR8 2 C(0)NR82’ 82‘, -SR82 , -S(0)Rs2, -S(0) 2 R82, CN, naioaikyi, haloalkoxy, -C(0)0Rs2, -C(0)NRs2R82’, -OCH2CH2OR82,

NR82S(0)2NR82'R82” and -C(CH3)20R82; wherein R 82 , Re 2 · and Rs 2" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

alternatively, Rs and Rs· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in Rs-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 83 , -ORe3, - NO2, -NR83R83', -NR83C(0)R83’, -NR83S(0)2R83’, -S(0)2NRe3R83',

NR83C(0)NR83’R83”, -SR83 , -S(0)Re3, -S(0) 2 R83, — CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R83·, -OCH 2 CH 2 OR8 3 ,

NR83S(0)2NR83’R83” and -C(CH3)20R83; wherein R 83 , Re 3 · and R 83 - are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 21 , -OR 21 , -NO 2 , -NR 21 R21', wherein R21, R21' and R 2 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R3 is selected from substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31 R31'; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 31 , -OR31, -NO2, -NR31R31', -NR 3i C(0)R 3 r, -NR 3i S(0) 2 R 3i’ , -S(0) 2 NR 3i R 3 r, - NR 3i C(0)NR 3 rR 3 r, -SR31 , -S(0)R 3i , -S(0) 2 R 31 , -CN, haloalkyl, haloalkoxy, -C(0)OR 3 I, -C(0)NR 3i R3r, -OCH 2 CH 2 OR 31 ,

NR 3i S(0) 2 NR 3 rR3r and -C(CH3) 2 OR3i ;

wherein R31, R 31' and R 3 r are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 ·, if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR 32 R 32 ·; wherein R 32 and R 32 · are independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted C 2- e alkenyl, and substituted or unsubstituted C 2- e alkynyl;

R 4 and R 4' are independently selected from halogen, -R I , -OR 4 I , -NO2, -NR i R r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R r , -NR 4i C(0)NR 4r R 4 r, -SR 4i , -S(0)R i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R 4 r, -OCH 2 CH 2 OR 4 I , - NR 41 S(0) 2 NR rR r and -C(CH 3 ) 2 OR I ; wherein R 4 I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -ORI 3 , halogen, -CN, haloalkyl, haloalkoxy and -NRI 3 RI 3 ·; wherein RI 3 and RI 3 · are independently selected from hydrogen, unsubstituted Ci -6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2- e alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -RI 4 , -ORI 4 , -N0 2 , -NRI 4 RI 4 ·, - NRI 4 C(0)RI ', -NRI 4 S(0) 2 RI 4 ·, -S(0) 2 NRI 4 RI 4' , - NRi 4 C(0)NR 14 R 14 ' , -SR 14 , -S(0)Ri 4 , - S(0) 2 RI 4 , -CN, haloalkyl, haloalkoxy, -C(0)0RM, -C(0)NRI RI 4 ·, -OCH 2 CH 2 ORI 4 , - NR 14 S(0) 2 NRI RI " and -C(CH 3 ) 2 ORI ; wherein Ru, R^ and R I4 - are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a )

wherein Ri, R 3 , R 3 , R 4 , R 4 ·, Rg, Rg·, X, Ui, Y2 and n are as defined in the detailed description, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture Of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a )

wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH2]pC(0)[CH 2 ] q -, -[CH2]pC(0)N(R z )[CH2]q-, - [CH 2 ]pN(Rz)C(0)[CH 2 ] q - and -[CH 2 ]pN(Rz)[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2 -e alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl; R z is selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-e alkyl; p is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(RI Q RIO )-; wherein R 10 and Ri 0 are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 10 and R 10’ may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y 2 is— C(Rio”Rio ) l wherein R 10 · and Rio · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, Rio- and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs·, Rs- and R 5 are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R5 and Rs· and/or R 5 · and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

Re, Re·, Re·· and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 6 and R 6' and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and R 6 and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Re is selected from substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re· is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and R 8 · taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R 3 is selected from substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

R 3' is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 4 and R 4 · are independently selected from halogen, -R 4 I , -OR 4 I , -N0 2 , -NR 4i R r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R r, -S(0) 2 NR 4 I R 4 V, -NR 4i C(0)NR 4r R 4r , -SR 4i , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R 4 r, -OCH 2 CH20R 4 I , - NR 4i S(0) 2 NR 4 rR r and -C(CH 3 ) 2 OR 4 I ; wherein R I , R 4 r and R r are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 9 and R 9 · are independently selected from hydrogen, halogen, -R 21 , -OR 21 , -NO2, - NR21 R21’, -NR 21 C(0)R21·, -NR2I S(0)2R21', -S(0)2NR2iR2i', - NR2iC(0)NR 2 rR 2 r, -SR21 , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH 2 CH 2 OR 2I , -NR 2i S(0) 2 NR 2r R 2 r and -C(CH 3 ) 2 OR 21 ; wherein R 2I , R 2 r and R 2 r are independently selected from hydrogen, substituted or unsubstituted C alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a )

wherein

X is selected from a bond, -[C(R a R b )] P -, -[CH 2 ]pC(0)[CH2] q -, -[CH 2 ]pC(0)N(Rz)[CH2] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -; R a is selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

Rb is selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci.6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is O, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(RioRio)-; wherein R10 and Ri 0 are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y 2 is— C(Rio' io )-l wherein R 10” and R 10 - are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2 - 6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, Ri<r and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R 5 , Re·, R 5” and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 - 6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 5 and R 5 · and/or R 5” and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs-, if substituted, is substituted with one or more substituent/s selected from -OR51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R 5 -R 5' and/or R 5 -R 5” , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 51 , -OR51, -NO2, -NRsiRsr, -NR 5i C(0)R 5 r, -NR 51 S(0)2R 5 r, -S(0) 2 NR5iR 5 r, - NR 5i C(0)NR 5 rR5r , -SR51 , -S(0)R 5i , -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0Rsi, -C(0)NR 5i R 5 r, -OCH2CH2OR51 , NR 5i S(0) 2 NR 5 rR5r and -C(CH 3 ) 2 OR5i;

wherein R 51 , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 6 , R 6' , R 6" and R 6 - are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 6 and R 6 · and/or R 6” and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R 6 and/or Re- and R 6 - taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re- and Re-, if substituted, is substituted with one or more substituent/s selected from -OR 61 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr; wherein the cycloalkyl, as defined in F Re· and/or fV-Re”·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 6 I ,

wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C2.6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 7i , -OR 7I , -NO2, -

NR 7i S(0)2NR 7 rR 7i” and -C(CH 3 ) 2 0R 7 I ; wherein R I , R r and R 7 r are independently selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2 -e alkynyl;

Re is selected from substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -OR 8I , halogen, -CN, haloalkyl, haloalkoxy and -NR 8i R 8 r; wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8I , -OR 8I , -NO2, -NR 8i R 8i’ , -NR 8i C(0)R 8 r, -NR 8i S(0)2R 8 r, -S(0)2NR 8i R 8 r, - NR 8i C(0)NR 8i' R 8i " , -SRei , -S(0)Rei, -S(0) 2 R 8i , -CN, haloalkyl, haloalkoxy, -C(0)OR 8I , -C(0)NR 8i R 8 , -OCH 2 CH 2 OR 8I ,

NR 8i S(0)2NR 8 rR 8 r’ and -C(CH3)20R 8 I ;

wherein R 8 I , Rer and Rsr are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

Re· is selected from hydrogen, substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in Re·, if substituted, is substituted with one or more substituent/s selected from -OR 82 , halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R 82" ; the cyclolakyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 82 , -OR 82 , -NO2, -NR 82 R 82’ , -NR 82 C(0)R 82' , -NR 82 S(0) 2 R 82' , -S(0) 2 NR 82 R 82' , - N R 82 C(0) N R 8 2'R 8 2” , -SR 82 , -S(0)R 82 , -S(0)2R 82 , - CN, haloalkyl, haloalkoxy, -C(0)0R 82 , -C(0)NR 82 R 82' , -OChfeCI-feOR^,

NR 82 S(0) 2 NR 82' R 82" and -C(CH3)20R 82 ; wherein R 82 , R 8 2 and R 82 ” are independently selected from hydrogen, substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

alternatively, Re and Rs· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in Re-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 83 , -ORe3, - NO2, -NR83R83', -NRe3C(0)Re3', -NRe3S(0)2Re3’, -S(0)2NRe3R83’,

NRe3C(0)NRe3’R83", -SR 8 3 , -S(0)R 83 , -S(0)2R 83 , — CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R 83' , -OCH 2 CH 2 OR 83 ,

NR 83 S(0) 2 NR 83' R 83 ' and -C(CH3)20R 83 ; wherein R 83 , R 8 3· and R 8 3- are independently selected from hydrogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R3 is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R3, if substituted, is substituted with one or more substituent/s selected from -OR31, halogen, -CN, haloalkyl, haloalkoxy and -NR31 R31'; wherein the cycloalkyl in R3, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R31, -OR 3 I , -NO 2 , -NR 3i R 3 r, -NR 3i C(0)R 3 r, -NR 3i S(0) 2 R3r, -S(0)2NR3iR3r, - NR 3i C(0)NR 3 rR3r, -SR31 , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)OR3i, -C(0)NR3iR3r, -OCH2CH2OR31,

NR3iS(0)2NR3i'R3i and -C(CH3)20R3i ;

wherein R 3I , R 3 t and R 3r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 ·, if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R 32 and R 32' are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R 4 I , -OR 4 I , -NO 2 , -NR 4i R 4 r, - NR 4i C(0)R 4r , -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R 4 r, -NR 4i C(0)NR 4r R 4r , -SR 4i , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR i R 4r , -OCH 2 CH 2 OR I , - NR 4i S(0) 2 NR 4 R 4r and -C(CH 3 ) 2 OR I ; wherein R 4 I , R r and R r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R 9 and Rg- are independently selected from hydrogen, halogen, -R 2 I , -OR21 , -NO2, - NR21 R21’, -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2i R2i”, -SR21 , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r OCH2CH2OR21, -NR2iS(0) 2 NR 2 rR 2 r and -C(CH 3 ) 2 OR2i; wherein R 21 , R 21 · and R 21 ·· are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2 -e alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR13, halogen, -CN, haloalkyl, haloalkoxy and -NRI 3 RI 3 ·; wherein R 13 and R 13’ are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C2-6 alkenyl, and unsubstituted C2-6 alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -RM, -OR14, -N0 2 , -NRMR ·, - NRi 4 C(0)Ri4', -NRi 4 S(0) 2 Ri4·, -S(0) 2 NRi 4 Ri4', - NRi 4 C(0)NRi4'Ri4', -SRM , -S(0)Ri 4 , - S(0) 2 Ri4, -CN, haloalkyl, haloalkoxy, -C(0)0R 14 , -C(0)NRi 4 Ri4', -OCH 2 CH 2 ORI 4 , - NRi 4 S(0)2NRi4'Ri4” and -C(CH 3 ) 2 ORI 4 ;

wherein R14, Ri b and R - are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C2-6 alkenyl, unsubstituted C2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a ’)

wherein Ri, R 3 , R 3 , R 4 , R 4 ·, R 9 , R 9' , X and n are as defined in the detailed description, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a ’)

wherein

X is selected from a bond, -[C(R a R b )]p-, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-e alkyl; p is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5; n is 0 or 1 ;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R 5 , Rs·, Rs and R 5 are independently selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R5 and Rs· and/or Rs- and Rs-· taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2.6 alkynyl; alternatively, Re and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and Re· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

R 8 is selected from substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C 2- s alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re· is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R3 is selected from substituted or unsubstituted C-i-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

R3' is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R I , -OR 4 I, -NO 2 , -NR 4i R r , - NR 4i C(0)R 4 r, -NR i S(0) 2 R 4 r, -S(0) 2 NR 4i R r , -NR 4i C(0)NR 4r R 4 r, -SR 4 I , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4 I R I , -OCH2CH 2 OR 4 I , - NR 4i S(0) 2 NR 4 rR 4 r and -C(CH 3 ) 2 0R 4 I ; wherein R I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; R g and R g · are independently selected from hydrogen, halogen, -R21, -OR21, -NO2, - NR 21 R 21' , -NR 2i C(0)R 2 r, -NR 2i S(0)2R 2 r, -S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 r, -SR 21 , -S(0)R 2i , -S(0) 2 R 2i , -CN, haloalkyl, haloalkoxy, -C(0)0R2i, -C(0)NR 2i R2r, - OCH 2 CH 2 OR 21 , -N R 21 S(0) 2 N R 2 r R 2 r and -C(CH 3 ) 2 OR2i; wherein R 21 , R 2 r and R 21” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2- 6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l a ’)

wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH 2 ] P C(0)[CH2]q-, -[CH2]pC(0)N(Rz)[CH 2 ]q-, - [CH 2 ]pN(Rz)C(0)[CH 2 ] q - and -[CH2]pN(R z )[CH 2 ] q -; R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2 .s alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2- e alkenyl, substituted or unsubstituted C 2.6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-e alkyl; p is 0, 1 , 2, 3, 4 or 5; q is O, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Ri is wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs-, Rs" and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R5 and Rs· and/or R 5 - and Rs - taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs-, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R 5 -R 5' and/or R 5 -R 5” , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 51 , -OR51, -NO2, -NRsiRsr, -NR 5i C(0)R 5 r, -NR 5 IS(0) 2 R 5 I ·, -S(0) 2 NR 5i R5i·, - NRsiCiOJNRsrRsr, -SR51 , -S(0)Rsi, -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0Rsi, -C(0)NR 5i R 5 r, -OCH2CH2OR51,

NRsiSiOJzNRsrRsr and -C(CH 3 ) 2 OR 5 I ;

wherein R 51 , Rsr and R 51 are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R6 and R6· and/or R6- and R6- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and R 6 · and/or Re- and Re - taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re- and F¾6 -, if substituted, is substituted with one or more substituent/s selected from -OR 61 , halogen, - CN, haloalkyl, haloalkoxy and -NReiRer;

wherein the cycloalkyl, as defined in Re-Re· and/or Re-Re-', if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 6 I , -OR61, -NO2, -NR61R6I', -NReiC(0)Rer, -NR6iS(0)2R6i·, -S(0)2NR 6i R6i’, - NR6iC(0)NR6i'Rer, -SR 6 I , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NR 6i Rer, -OCH 2 CH 2 OR6i, NR6iS(0)2NR6i'R6i” and -C(CH3)20R6i ; wherein Rei, Rev and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R71, -OR71, -NO2, - NR71R71·, -NR 7i C(0)R 7 r, -NR 7i S(0) 2 R7r, -S(0) 2 NR 7i R7r,

NR 7i C(0)NR 7 rR7i ", -SR71 , -S(0)R 7I , -S(0) 2 R 71 , -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR7iR 7i" , -OCH2CH2OR71,

NR7iS(0) 2 NR 7 rR7r and -C(CH 3 ) 2 OR7i; wherein R 71 , R 71 · and R 71 · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 8 is selected from substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2- 6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -ORsi, halogen, -CN, haloalkyl, haloalkoxy and -NRsiRer; wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 I , -OR 8 I , -NO2, -NR 8i R 8 r, -NR 8i C(0)R 8 r, -NR 8 IS(0)2R 8 I’ I -S(0)2NR 8i R 8 r, - NR 8i C(0)NR 8 rR 8i , -SRm , -S(0)R 8 I , -S(0) 2 R 8i , -CN, haloalkyl, haloalkoxy, -C(0)0R 8i , -C(0)NR 8i R 8r , -OCH 2 CH 2 OR 8I ,

NR 8i S(0) 2 NR 8 rR 8i " and -C(CH3)20R 8I ; wherein R 8I , Rsr and R 8 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; Re· is selected from hydrogen, substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in Re·, if substituted, is substituted with one or more substituent/s selected from -OR 82 , halogen, -CN, haloalkyl, haloalkoxy and -NR 8 2R 8 2'; the cyclolakyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 2, -OR 82I -NO2, -NR 8 2R 8 2', -NR 82 C(0)R 82' , -NR 82 S(0) 2 R 82' , -S(0) 2 NR 82 R 82 ·, - N R 82 C(0) N R 8 2'R 8 2 , -SR 82 , -S(0)R 82 , -S(0)2R 82 , — CN, haloalkyl, haloalkoxy, -C(0)OR 82 , -C(0)NR 82 R 82' , -0CH 2 CH20R 82 , NR 82 S(0) 2 NR 82' R 82" and -C(CH3)20R 82 ; wherein R 8 2, R 8 2· and R 8 2- are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

alternatively, R 8 and R 8 · taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in R 8 -R 8 ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 83 , -OR 83 , - NO2, -NR 83 R 83' , -NR 83 C(0)R 83' , -NR 83 S(0) 2 R 83' , -S(0) 2 NR 83 R 83' , NR 83 C(0)NR 83' R 83 " , -SR 83 , -S(0)R 83 , -S(0) 2 R 83 , -CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R 83' , -0CH2CH20R 83 ,

NR 83 S(0)2NR 83 , R 83" and -C(CH3)20R 83 ; wherein R 83 , Rs 3 and R 83" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 3 is selected from substituted or unsubstituted Ci- b alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 a!kyny!, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31R31'; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R31, -OR31, -NO2, -NR31R31’, -NR 3i C(0)R 3 r, -NR 3i S(0) 2 R3i·, -S(0)2NR3iR3r, - NR 3i C(0)NR 3 rR3r, -SR31 , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)0R 3i , -C(0)NR 3i R 3 r, -OCH2CH2OR31,

NR 3i S(0) 2 NR 3 rR 3i” and -C(CH 3 ) 2 0R 3i ;

wherein R 31 , R 31’ and R 3 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3' , if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R 32 and R 37 are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R 4 I, -OR 4I , -NO2, -NR 4i R 4 r, - NR 4i C(0)R r, -NR 41 S(0) 2 R 4 r, -S(0) 2 NR 4i R 4r , -NR 41 C(0)NR 4r R 4 r, -SR I , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR i R r, -OCH 2 CH 2 OR I , - NR 4i S(0) 2 NR 4 rR 4i - and -C(CH 3 ) 2 OR I ; wherein R 4 I, R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2-6 alkynyl;

Rg and Rg· are independently selected from hydrogen, halogen, -R 2I , -OR 2I , -N0 2 , - NR 2i R 2 r, -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R 2 r, -S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 -r, -SR 2I , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH 2 CH 2 OR 2I , -NR 2I S(0) 2 NR 2I’ R 2I " and -C(CH3) 2 OR 2I ; wherein R 2I , R 2 r and R 2 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2- e alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR 13 , halogen, -CN, haloalkyl, haloalkoxy and -NR13R 13' ; wherein R 13 and R 13 are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2.6 alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -Ru, -OR I4 , -NO2, -NR I4 R I4 ·, - NR I4 C(0)R I4 ·, -NR 14 S(0) 2 R I4 ·, -S(0) 2 NR I4 R 14 ·, - NR I4 C(0)NR I4 RI 4 ' , -SRI 4 , -S(0)Ri 4 , - S(0) 2 R I4 , -CN, haloalkyl, haloalkoxy, -C(0)OR I4 , -C(0)NR I4 R I 4 ·, -OCH 2 CH 2 ORI 4 , - NR I4 S(0) 2 NR I4 R I4 " and -C(CH 3 ) 2 0R I4 ;

wherein R I4 , R and R I4 - are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C2-6 alkenyl, unsubstituted C2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b )

wherein Ri, R 3 , R 3 ·, R 4 , R 4 , Rg, Rg·, X, Yi, Y2 and n are as defined below in the detailed description, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b )

wherein

X is selected from a bond, -[C(R a Rb)] P -, -[CH2] P C(0)[CH 2 ]q-, -[CH2] P C(0)N(R z )[CH 2 ]q-, - [CH 2 ] P N(Rz)C(0)[CH 2 ] q - and -[CH 2 ] P N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2 -e alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and Ru, taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -

C(0)-Ci- 6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is O, 1 , 2, 3, 4 or 5;

n is O oM ;

Yi is— C(RioRio)-; wherein R1 0 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2- 6 alkenyl and substituted or unsubstituted C2.6 alkynyl; alternatively, R10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y2 is— C(Rio"Rio”)-; wherein Rio- and Rio- are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rio · and R10- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R5, Rs·, Rs" and Rs” are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 5 and Rs· and/or R 5” and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

R 6 , R 6' , Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2 -e alkynyl; alternatively, Re and Re· and/or Re·· and Re · taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and Re· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Re is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re· is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, Re and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R 3 is selected from substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

R 3 is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R 4I , -OR 4I , -NO2, -NR 4i R 4 r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R 4 r, -NR 41 C(0)NR 4i R 4r , -SR 4I , -S(0)R 41 , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4I , -C(0)NR 4i R 4r , -OCH 2 CH 2 OR 4I , - NR 4i S(0) 2 NR 4 rR4r· and -C(CH3)20R 4i ; wherein R I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R9 and Rg- are independently selected from hydrogen, halogen, -R21, -OR21, -NO2, - NR21R21’, -NR 2i C(0)R 2 r, -NR2iS(0)2R2i\ -S(0)2NR2iR2r, - NR2iC(0)NR2rR2i”, -SR21 , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2r , - OCH 2 CH 2 OR 2I , -NR 2i S(0) 2 NR 2 rR 2i” and -C(CH3) 2 OR 2I ; wherein R 2I , R 2 r and R 2 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b )

wherein X is selected from a bond, -[C(R a Rb)] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ]pN(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted C-ve alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C å -e alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2.6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; p is O, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

Yi is— C(R-ioRio')-; wherein Rio and Rio are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2- e alkynyl; alternatively, Rio and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Y 2 is— C(Rio 'Rio’ " )-; wherein Rio- and Rio- are independently selected from hydrogen, substituted or unsubstituted Ci. 6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rio- and RKT may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

Ri is wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs', Rs- and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rs and Rs· and/or Rs- and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R5, Rs· Rs- and Rs-, if substituted, is substituted with one or more substituent/s selected from -OR51, halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R5-R5' and/or Rs-Rs”, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -NO2, -NRsiRsr, -NR 5i C(0)R 5 r, -NR 5i S(0) 2 Rsr, -S(0) 2 NR5iR 5 r, - NR5iC(0)NR 5 rR5i”, -SR51 , -S(0)Rsi, -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0R5i, -C(0)NRsiRsr, -OCH 2 CH 2 OR5i, NR5iS(0) 2 NR 5 rR 5 r and -C(CH 3 ) 2 OR 5 I ;

wherein R51, Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl;

R 6 , Re·, R 6” and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 6 and R 6 · and/or R 6” and R 6 -· taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R 6 · and/or R 6 - and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , R 6 · Re- and Re ·, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr; wherein the cycloalkyl, as defined in Re-Re· and/or Re-Re· , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -OR61, -N0 2 , -NR61R6I , -NR 6i C(0)R 6 r, -NR6iS(0) 2 Rer, -S(0) 2 NR6iR6r, - NReiC(0)NR 6 rR6i ", -SRei , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0R 6i , -C(0)NR 6i Rei , -OCH 2 CH 2 OR 6 I , NR 6i S(0) 2 NR6i R6i” and -C(CH3) 2 OR6i ; wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2 -e alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 7I , -OR 7I , -NO2, - R 7r , haloalkyl, haloalkoxy, -C(0)0R i , -C(0)NR 7i R 7r , -OCH 2 CH 2 OR 7I ,

NR 7i S(0) 2 NR 7 R 7r and -C(CH 3 ) 2 OR 7I ; wherein R 7I , R 7 r and R 7 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

Re is selected from substituted or unsubstituted alkyl, substituted or unsubstituted C 2- e alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in Re, if substituted, is substituted with one or more substituent/s selected from -OR 8 I , halogen, -CN, haloalkyl, haloalkoxy and -NRsiRar; wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 I , -OR 8 I , -NO2, -NReiRer, -NR 8i C(0)R 8 r, -NR 8i S(0) 2 R 8i' , -S(0)2NR 8i R 8 r, - NR 8i C(0)NR 8 rR 8 r, -SR 81 , -S(0)R 8i , -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)OR 8 I , -C(0)NR 8i R 8r , -OCH 2 CH 2 OR 8 I ,

NR 8i S(0) 2 NR 8i ' R 8i” and -C(CH3)20R 8 I ; wherein R 8 I , R 8 r and R 8 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

Re· is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -OR 82 , halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R 8 2'; the cyclolakyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 2, -OR 82 , -NO2, -NR 8 2R 8 2\ -NRS2C(0)R 82’ , -NR 8 2S(0)2R82’, -S(0) 2 NR 82 R 82’ , - NR 82 C(0)NR 82' R 8 2 ", -SR 8 2 , -S(0)R 82 , -S(0)2R 82 , — CN, haloalkyl, haloalkoxy, -C(0)0R 82 , -C(0)NR 82 R82', -OCH2CH 2 OR 82 ,

NR 82 S(0) 2 NR 82' R 82” and -C(CH3)20R 82 ; wherein R 82 , R 8 2· and R 82 · are independently selected from hydrogen, substituted or unsubstituted Ci. 8 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-8 alkynyl;

alternatively, R 8 and R 8 · taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in R 8 -R 8 ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 3, -OR 8 3, -

NO2, -NR 83 R 83' , -NR 83 C(0)R 83' , -NR 83 S(0) 2 R 83’ , -S(0) 2 NR 83 R 83’ ,

NR 83 C(0)NR 83' R 8 r, -SR 83 , -S(0)R 83 , -S(0)2Re3, — CN, haloalkyl, haloalkoxy, -C(0)0Rs3, -C(0)NR 83 R83’, -OCH2CH2OR83,

NR 83 S(0)2NR 83 R 83 · and -C(CH3)20R 83 ; wherein R 83 , R 83 · and R 83 - are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

R3 is selected from substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R3, if substituted, is substituted with one or more substituent/s selected from -OR31, halogen, -CN, haloalkyl, haloalkoxy and -NR31R31'; wherein the cycloalkyl in R3, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R31, -OR31, -NO2, -NR31R31’, -NR 3i C(0)R 3 r, -NR3iS(0)2R3i’, -S(0)2NR3iR3-r, - NR3iC(0)NR 3 rR3i”, -SR31 , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)0R 3i , -C(0)NR 3i R 3 r, -OCH2CH2OR31,

NR3iS(0) 2 NR 3 rR3i" and -C(CH3)20R3i;

wherein R 31 , R 31' and R 31" are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R 32 and R 32' are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R 4 I , -OR 4 I, -N0 2 , -NR 4i R r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R 4r , -NR 4i C(0)NR 4r R 4r , -SR 4 I , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR 4i R 4 r, -OCH 2 CH 2 OR 4 I , - NR 4i S(0) 2 NR 4r R 4r and -C(CH 3 ) 2 OR 41 ; wherein R 4I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl; R 9 and Rg· are independently selected from hydrogen, halogen, -R 2I , -OR 2I , -N0 2 , - NR 2i R 2 r, -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R 2 r, -S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 r', -SR 2I , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2I , -C(0)NR 2i R 2 , - OCH 2 CH 2 OR 2i , -NR 2i S(0) 2 NR 2r R 2r and -C(CH 3 ) 2 OR 2I ; wherein R 2I , R 2 r and R 2 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR13, halogen, -CN, haloalkyl, haloalkoxy and -NRI 3 RI 3 ·; wherein RI 3 and RI 3 · are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C 2 -e alkenyl, and unsubstituted C 2-6 alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -R14, -OR14, -N0 2 , -NR14R14', - NRi 4 C(0)Ri4·, -NRI 4 S(0) 2 RI4·, -S(0) 2 NR 14 Ri4', - NRi 4 C(0)NRi4'Ri4", -SR14 , -S(0)Ri 4 , - S(0) 2 Ri4, -CN, haloalkyl, haloalkoxy, -C(0)0Ri 4 , -C(0)NR 14 Ri4·, -OCH 2 CH 2 ORI 4 , - NRI4S(0) 2 NRI 4 RI4" and -C(CH 3 ) 2 ORI 4 ;

wherein R14, Ri b and Ru- are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2 -e alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b ’)

(l b ), wherein Ri, R 3 , R 3' , R 4 , R 4 ·, R 9 , R 9' , X and n are as defined below in the detailed description, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b ’)

wherein

X is selected from a bond, -[C(R a R b )] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(Rz)C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2 .e alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2.6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2.6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; p is 0, 1 , 2, 3, 4 or 5; q is 0, 1 , 2, 3, 4 or 5; n is 0 or 1 ;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

R 5 , Rs·, Re·' and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R5 and Rs- and/or Rs- and Rs ·· taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Re and Re· and/or R 6 - and R 6 · taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R6· and/or R 6 and Re - taken together with the carbon atom to which they are attached may form a carbonyl group;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Re is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-0 alkenyl, substituted or unsubstituted C 2 -s alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;

Re· is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 -6 alkenyl, substituted or unsubstituted C 2- 6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; alternatively, R 8 and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl;

R 3 is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted a Iky I cycloalky I;

R 3' is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 4 and R 4' are independently selected from halogen, -R41, -OR41, -NO2, -NR41R41', - NR 4i C(0)R 4i' , -NR 4i S(0) 2 R4r, -S(0) 2 NR 4i R4r, -NR 4i C(0)NR 4 rR4r, -SR41 , -S(0)R 4i , - S(0) 2 R 4i , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R4i·, -OCH2CH2OR41, - NR4iS(0) 2 NR 4 rR4r and -C(CH 3 ) 2 OR 4 I ; wherein R 41 , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; Rg and Rg- are independently selected from hydrogen, halogen, -R21, -OR21, -N0 2 , - NR21R21’, -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2rR2i”, -SR21 , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH2CH2OR21, -NR2iS(0)2NR 2 rR 2 r' and -C(CH 3 ) 2 OR 2I ; wherein R21, R21· and R 2 r are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (l b ’)

(I b ), wherein X is selected from a bond, -[C(R a R b )] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(Rz)C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R z is selected from hydrogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C 2- e alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci-e alkyl; p is 0, 1 , 2, 3, 4 or 5; q is O, 1 , 2, 3, 4 or 5;

n is 0 or 1 ;

wherein m is 0, 1 or 2; r is 0, 1 or 2; t is 0, 1 , 2, 3, 4 or 5;

Rs, Rs , Rs- and R 5 " are independently selected from hydrogen, halogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 5 and Rs· and/or Rs- and R 5 - taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs ·, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R 5 -R 5' and/or R 5 -R 5 , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 51 , -OR51, -NO2, -NR51R51', -NR 5i C(0)R 5 r, -NR 5i S(0) 2 R5i', -S(0) 2 NR5iR 5 r, - NR 5i C(0)NR 5i' R 5 r, -SR51 , -S(0)R 5i , -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0R 5i , -C(0)NR 5i R 5 r, -OCH2CH2OR51,

NR5iS(0) 2 NR 5 rR5r and -C(CH 3 ) 2 OR5i ;

wherein R 51 , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; Re, Re·, Re·· and R 6 - are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 6 and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R 6 · and/or R 6 ·· and Re- taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in Re, Re· Re- and Re- if substituted, is substituted with one or more substituent/s selected from -OR 61 , halogen, - CN, haloalkyl, haloalkoxy and -NReiRer;

wherein the cycloalkyl, as defined in Re-Re· and/or Re-Re-, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 6 I ,

-OR61, -NO2, -NR61R6I', -NReiC(0)Rer, -NR6iS(0)2R6i·, -S(0)2NR6iRer, - NReiC(0)NR6rRer, -SR 6 I , -S(0)Rei, -S(0) 2 R 6i , -CN, haloalkyl, haloalkoxy, -C(0)0R6i, -C(0)NR6iRer, -OCH2CH2OR61, NR6iS(0)2NR6rR6r and -C(CH3)20R6i; wherein Rei, Rer and Rer· are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R71, -OR71, -NO2, - NR71R71', -NR 7i C(0)R 7 r, -NR7iS(0) 2 R 7 r, -S(0) 2 NR 7i R7r,

NR 7i C(0)NR7i R7i ", -SR71 , -S(0)R 7 I , -S(0) 2 R 7 I, -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR 7i R 7 r, -OCH2CH2OR71,

NR7iS(0) 2 NR 7 rR7r and -C(CH 3 )20R 7 I ; wherein R71, R71’ and R71” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 8 is selected from substituted or unsubstituted C 1 -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in Re, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, -CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl defined in Re, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -ORei, -NO2, -NReiRer, -NReiC(0)Rer, -NReiS(0)2Rer, -S(0)2NReiRer, - NR 8i C(0)NRerR8r, -SRei , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)OR 8 I , -C(0)NR 8i Rer, -OCH 2 CH 2 ORei, NReiS(0)2NRerR 8i” and -C(CHe)20Rei;

wherein Rei , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl; Re· is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C 2-8 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in Re·, if substituted, is substituted with one or more substituent/s selected from -ORs2, halogen, -CN, haloalkyl, haloalkoxy and -NR 82 Re2 ; the cyclolakyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rs 2 , -ORe2, -NO2, -NR82R82', -NR82C(0)R82’, -NR82S(0)2R82', -S(0)2NR82R82', - NR 8 2C(0)NR82'R82 ", -SRS2 , -S(0)R 82 , -S(0) 2 R 82 , -CN, haloalkyl, haloalkoxy, -C(0)0Re2, -C(0)NR 82 R82·, -OCH2CH2OR82,

NR82S(0)2NR82'R82’’ and -C(CH3)20Re2! wherein R 82 , Rs 2 · and Re 2 ·· are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

alternatively, Re and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in Re-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Re3, -ORe3, - NO2, -NR83R83’, -NR83C(0)R83’, -NR 83 S(0) 2 R83·, -S(0)2NR83R83',

NR 83 C(0)NR 83 R83", -SRes , -S(0)R 83 , -S(0) 2 R 83 , -CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R83·, -OCH2CH2OR83,

NR83S(0)2NR83'R83 ' and -C(CH3)20R83; wherein Re 3 , Rs 3’ and Re 3 · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R 3 is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 a!kynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31R31'; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 31 , -OR31, -NO2, -NR31R31’, -NR 3i C(0)R 3 r, -NR3iS(0)2R3i’, -S(0)2NR3iR3r, - NR 3i C(0)NR 3 rR3i", -SR31 , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -OCH2CH2OR31,

NR3iS(0) 2 N

wherein R 31 , R 31' and R 31" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 3' is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2 -6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3' , if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR 3 2R32·; wherein R 32 and R 32 · are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

R4 and R 4' are independently selected from halogen, -R41, -OR41, -NO2, -NR41R41', - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R4i , -NR4iC(0)NR 4 vR 4 r, -SR41 , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4 I R 4 I , -OCH 2 CH 2 OR 4 I , - NR 4i S(0) 2 NR 4 rR4r and -C(CH 3 ) 2 OR 4 I ; wherein R41, R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 .e alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R 9 and Rg· are independently selected from hydrogen, halogen, -R 2I , -OR 2I , -N0 2 , - NR 2i R 2 r, -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R 2 r, -S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 r, -SR 2I , -S(0)R 2I , -S(0) 2 R 2I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH 2 CH 2 OR 2I , -NR 2i S(0) 2 NR 2i' R 2i” and -C(CH 3 ) 2 OR 2I ; wherein R 2I , R 2 r and R 2 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -ORI 3 , halogen, -CN, haloalkyl, haloalkoxy and -NRI 3 RI 3 ·; wherein RI 3 and RI 3 · are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2 -e alkynyl;

the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -R14, -OR14, -N0 2 , -NR14R14', - NRi 4 C(0)Ri 4' , -NRI 4 S(0) 2 R 14' , -S(0) 2 NRI 4 R 14' , - NRI 4 C(0)NR I4 .R 14" , -SR H , -S(0)Ri 4 , - S(0) 2 R I4 , -CN, haloalkyl, haloalkoxy, -C(0)0Ri 4 , -C(0)NR I4 R I4 ·, -OCH 2 CH 2 OR I4 , - NR I4 S(0) 2 NR I4 R I4 · and -C(CH 3 ) 2 OR I4 ;

wherein R , R™· and Ri are independently selected from hydrogen, unsubstituted

Ci- 6 alkyl, unsubstituted C2-6 alkenyl, unsubstituted C2-6 a!kyny!, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

For clarity purposes, all groups and definitions described in the present description and referring to compounds of general Formula (I), also apply to compounds of general Markush Formulae (G), (l a ), (l a ), (l b ) and (l b ), (where applicable), and to all intermediate of synthesis, when those groups are present in the mentioned general Markush formulae, since compounds of general Markush Formulae (G), (l a ), (l a ), (l b ) and (l b ), are included within the scope of the larger definition of general Markush Formula (I).

For clarity purposes, the general Markush Formula (I)

is equivalent to

wherein only - CH 2 - is included into the brackets, and n means the number of times that -CH 2 - is repeated. The same would apply, when applicable, to general Markush Formulae (I), (I’), (l a ), (l a’ ), (l b ) and (l b ), and to all intermediates of synthesis.

In addition, and for clarity purposes, it should further be understood that naturally if n is 0, the oxygen atom and/or the phenyl group are still present, when applicable, in general Markush Formulae (I), (G), (l a ), (l a ), (l b ) and (l b ), and to all intermediates of synthesis.

For clarity purposes, the expression“the heterocyclyl in Rs-Re " means the heterocyclyl resulting when R 8 and Re form, together with the nitrogen to which they are attached, a heterocyclyl. This heterocyclyl can then be substituted or not. This definition is also generally applicable and can be also applied as a definition of any Other cycle (preferably cycloalkyl or heterocycl) formed from two different functional groups like e.g. “the cycle in Ri-Ri“ means the cycle resulting when R, and R,· form a cycle together with the atom(s) to which they are attached. This cycle can then be substituted or not.

For clarity purposes, reference is also made to the following statements below in the definitions of substitutions on alkyl etc. or aryl etc. that“wherein when different radicals R 1 to R 83 - are present simultaneously in Formula (I) they may be identical or different”. This statement is reflected in the below general Formula (I 3 ) being derived from and falling into the definition of R 1 within Formula (I), wherein R 5 , Rs·, Rs ·, Rs , R6, Re·, R6·, Re-, R7, Re, Re· and t are as defined in the description. In addition, R6 a , R6 b , R6 c , R6 d , m’ and r’ are added. As said above, this statement is thus reflected in that R6a, R6 b are or could be different from R6 and R6· or not. In the same way, R 6c and R 6d are or could be different from R 6 - and Re - or not. m’ being 0 or 1 and r’ being 0 or 1 naturally resulting from m being o, 1 or 2 or r being 0, 1 or 2.

The same would be applicable mutatis mutandis for general Formulas like general Formula (I) as well as the other general Formulas (I), (G), (l a ), (l a ), (l b ) and (l b ), above and to all intermediates of synthesis.

In the context of this invention, alkyl is understood as meaning saturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses e.g. -CH3 and -CH2-CH3. In these radicals, Ci-2-alkyl represents C1- or C2-alkyl, Ci-3-alkyl represents C1-, C2- or C3-alkyl, Ci-4-alkyl represents C1 -, C2-, C3- or C4-alkyl, Ci-s-alkyl represents C1-, C2-, C3-, C4-, or C5-alkyl, Ci-e-alkyl represents C1-, C2-, C3-, C4-, C5- or C6-alkyl, Ci-7-alkyl represents C1-, C2-, C3-, C4- , C5-, C6- or C7-alkyl, Ci-s-alkyl represents C1 -, C2-, C3-, C4-, C5-, C6-, C7- or C8- alkyl, Ci-10-alkyl represents C1-, C2-, C3-, C4-, C5-, C6-, C7-, C8-, C9- or C10-alkyl and Ci-18-alkyl represents C1-, C2-, C3-, C4-, C5-, C6-, C7-, C8-, C9-, C10-, C1 1-, C12-, C13-, C14-, C15-, C16-, C17- or C18-alkyl. The alkyl radicals are preferably methyl, ethyl, propyl, methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1 ,1-dimethylethyl, pentyl, 1 ,1-dimethylpropyl, 1 ,2-dimethylpropyl, 2,2-dimethylpropyl, hexyl, 1- methylpentyl, if substituted also CHF 2 , CF 3 or CH 2 OH etc. Preferably alkyl is understood in the context of this invention as Ci -8 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, or octyl; preferably is Ci -8 alkyl like methyl, ethyl, propyl, butyl, pentyl, or hexyl; more preferably is Ci- 4 alkyl like methyl, ethyl, propyl or butyl.

Alkenyl is understood as meaning unsaturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses groups like e.g. -CF CH-CH 3 . The alkenyl radicals are preferably vinyl (ethenyl), allyl (2-propenyl). Preferably in the context of this invention alkenyl is C 2 -io-alkenyl or C 2-8 -alkenyl like ethylene, propylene, butylene, pentylene, hexylene, heptylene or octylene; or is C2-6- alkenyl like ethylene, propylene, butylene, pentylene, or hexylene; or is C 2-4 -alkenyl, like ethylene, propylene, or butylenes.

Alkynyl is understood as meaning unsaturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses groups like e.g. -CfC-CF (1-propinyl). Preferably alkynyl in the context of this invention is C2- 10 - alkynyl or C 2-8 -alkynyl like ethyne, propyne, butyene, pentyne, hexyne, heptyne, or octyne; or is C 2-6 -alkynyl like ethyne, propyne, butyene, pentyne, or hexyne; or is C2-4- alkynyl like ethyne, propyne, butyene, pentyne, or hexyne.

In connection with alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl and O-alkyl - unless defined otherwise - the term substituted in the context of this invention is understood as meaning replacement of at least one hydrogen radical on a carbon atom by halogen (F, Cl, Br, I), -NRkRk·, -SRk, -S(0)Rk, -S(0)2Rk, -ORk, - C(0)R k , -C(0)OR k , -CN, -C(0)NR k R k \ haloalkyl, haloalkoxy, being R k represented by R13, R31, 32, R51, Rei, Rei or RS2 (being Rw represented by R13·, R31·, R32', Rsr, Rer, Rer or R 82'; being R k represented by R13 ”, R31 ”, R32”, Rsr, Rer, Rer· or R 82 ) ; wherein R1 to R 83 · and R z are as defined in the description, and wherein when different radicals R 1 to Re and R z are present simultaneously in Formula I they may be identical or different.

Most preferably in connection with alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl or O-alkyl, substituted is understood in the context of this invention that any alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl or O-alkyl which is substituted with one or more of halogen (F, Cl, Br, I), -NR k R k ·, -OR k , -CN, -SRk, haloalkyl, haloalkoxy, being Rk represented by R13, R31, R32, R51, Rei, Rei or RS2, (being R k · represented by RI 3 ·, R31', R32', Rsr, Rer, Rsr or R 82 ·; being Rk" represented by R13 R31 ", R32", Rsr, Rer, Rer or Ra2 ); wherein R1 to Re3- and R z are as defined in the description, and wherein when different radicals R1 to Re3” and R z are present simultaneously in Formula I they may be identical or different.

More than one replacement on the same molecule and also on the same carbon atom is possible with the same or different substituents. This includes for example 3 hydrogens being replaced on the same C atom, as in the case of CF 3 , or at different places of the same molecule, as in the case of e.g. -CH(OH)-CH=CH-CHCi2.

In the context of this invention haloalkyl is understood as meaning an alkyl being substituted once or several times by a halogen (selected from F, Cl, Br, I). It encompasses e.g. -CH 2 CI, -CH 2 F, -CHC , -CHF 2 , -CCI 3 , -CF3 and -CH2-CHCI2. Preferably haloalkyl is understood in the context of this invention as halogen- substituted Ci-4-alkyl representing halogen substituted C1-, C2-, C3- or C4-alkyl. The halogen-substituted alkyl radicals are thus preferably methyl, ethyl, propyl, and butyl. Preferred examples include -CH 2 CI, -CH 2 F, -CHCb, -CHF 2 , and -CF 3 .

In the context of this invention haloalkoxy is understood as meaning an -O-alkyl being substituted once or several times by a halogen (selected from F, Cl, Br, I). It encompasses e.g. -OCH2CI, -OCH2F, -OCHC , -OCHF2, -OCCI3, -OCF3 and - OCH2-CHCI2. Preferably haloalkyl is understood in the context of this invention as halogen-substituted -OCi. 4 -alkyl representing halogen substituted C1 -, C2-, C3- or C4- alkoxy. The halogen-substituted alkyl radicals are thus preferably O-methyl, O-ethyl, O-propyl, and O-butyl. Preferred examples include -OCH2CI, -OCH2F, -OCHCb, - OCHF2, and -OCF3.

In the context of this invention cycloalkyl is understood as meaning saturated and unsaturated (but not aromatic) cyclic hydrocarbons (without a heteroatom in the ring), which can be unsubstituted or once or several times substituted. Furthermore, C3-4- cycloalkyl represents C3- or C4-cycloalkyl, C 3 -5-cycloalkyl represents C3-, C4- or C5- cycloalkyl, C3-6-cycloalkyl represents C3-, C4-, C5- or C6-cycloalkyl, C3-7-cycloalkyl represents C3-, C4-, C5-, C6- or C7-cycloalkyl, C3-e-cycloalkyl represents C3-, C4-, C5- , C6-, C7- or C8-cycloalkyl, C4-5-cycloalkyl represents C4- or C5-cycloalkyl, C4-6- cycloalkyl represents C4-, C5- or C6-cycloalkyl, C 4 -7-cycloalkyl represents C4-, C5-, C6- or C7-cycloalkyl, Cs-e-cycloalkyl represents C5- or C6-cycloalkyl and C5-7-cycloalkyl represents C5-, C6- or C7-cycloalkyl. Examples are cyclopropyl, 2-methylcyclopropyl, cyclopropylmethyl, cyclobutyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cycloheptyl, cyclooctyl, and also adamantyl. Preferably in the context of this invention cycloalkyl is C3-ecycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; or is C 3- 7cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; or is C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, especially cyclopentyl or cyclohexyl.

Aryl is understood as meaning 5 to 18 (preferably 6 to 14) membered mono or polycyclic ring systems with at least one aromatic ring but without heteroatoms even in only one of the rings. Examples are phenyl, naphthyl, fluoranthenyl, fluorenyl, tetralinyl, dihydroindene or indanyl, 9H-fluorenyl or anthracenyl radicals, which can be unsubstituted or once or several times substituted. Most preferably aryl is understood in the context of this invention as phenyl, naphthyl or anthracenyl, preferably is phenyl.

A heterocyclyl radical or group (also called heterocyclyl hereinafter) is understood asmeaning - especially - 5 to 18 membered mono or polycyclic heterocyclic ring systems, with at least one saturated or unsaturated ring which contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring. A heterocyclic group can also be substituted once or several times.

An heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; In general, such a heterocyclyl may contain between 3 and 32 atoms in the rings (preferably 4 to 20 atoms in the rings, or most preferably 5 to 18 atoms in the rings). Thus, a heterocyclyl may contain between 3 and 12 atoms in the ring (preferably 4 to 10 atoms in the ring, or 5 to 8 atoms in the ring, or 5 to 6 atoms in the ring) in case of a heterocyclyl of one saturated or unsaturated ring. Such a heterocyclyl may also contain between 5 and 22 atoms in both rings together (preferably 6 to 16 atoms in both rings together, or 7 to 12 atoms in both rings together or 8 to 10 atoms in both rings together) in case of a heterocyclyl of two saturated or unsaturated rings. Such a heterocyclyl may also contain between 7 and 32 atoms in the 3 rings together (preferably 10 to 22 atoms in the three rings together, or 12 to 20 atoms in the three rings together or 10 to 18 atoms in the three rings together) in case of a heterocyclyl of three saturated or unsaturated rings.

Examples include non-aromatic heterocyclyls such as tetrahydropyrane, oxazepane, morpholine, piperidine, pyrrolidine as well as heteroaryls such as furan, benzofuran, thiophene, benzothiophene, pyrrole, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, phthalazine, thiazole, benzothiazole, indole, benzotriazole, carbazole and quinazoline.

Subgroups inside the heterocyclyls as understood herein include heteroaryls and non- aromatic heterocyclyls.

- the heteroaryl (being equivalent to heteroaromatic radicals or aromatic heterocyclyls, or also to “heterocyclyl containing at least one aromatic ring containing at least one heteroatom”) is an aromatic 5 to 18 membered mono or polycyclic heterocyclic ring system of one or more rings of which at least one aromatic ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a 5 to 18 membered mono or polycyclic aromatic heterocyclic ring system of one or two rings of which at least one aromatic ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from furan, benzofuran, thiophene, benzothiophene, pyrrole, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, phthalazine, benzothiazole, indole, benzotriazole, carbazole, quinazoline, thiazole, imidazole, pyrazole, oxazole, thiophene and benzimidazole;

- the non-aromatic heterocyclyl is a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or more rings of which at least one ring - with this (or these) ring(s) then not being aromatic - contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or two rings of which one or both rings - with this one or two rings then not being aromatic - contain/s one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepam, pyrrolidine, piperidine, piperazine, tetrahydropyran, morpholine, indoline, oxopyrrolidine, benzodioxane, especially is benzodioxane, morpholine, tetrahydropyran, piperidine, oxopyrrolidine and pyrrolidine.

Preferably in the context of this invention heterocyclyl is defined as a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring. Preferably it is a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring.

Preferred examples of heterocyclyls include oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, , benzofuran, benzimidazole, indazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, tetrahydroisoquinoline, phthalazine, benzo-1 ,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline, especially is pyridine, pyrazine, indazole, benzodioxane, thiazole, benzothiazole, morpholine, tetrahydropyrane, pyrazole, imidazole, piperidine, thiophene, indole, benzimidazole, pyrrolo[2,3b]pyridine, benzoxazole, oxopyrrolidine, pyrimidine, oxazepane and pyrrolidine.

In the context of this invention oxopyrrolidine is understood as meaning pyrrolidin-2- one.

In connection with aromatic heterocyclyls (heteroaryls), non-aromatic heterocyclyls, aryls and cycloalkyls, when a ring system falls within two or more of the above cycle definitions simultaneously, then the ring system is defined first as an aromatic heterocyclyl (heteroaryl) if at least one aromatic ring contains a heteroatom. If no aromatic ring contains a heteroatom, then the ring system is defined as a non-aromatic heterocyclyl if at least one non-aromatic ring contains a heteroatom. If no non-aromatic ring contains a heteroatom, then the ring system is defined as an aryl if it contains at least one aryl cycle. If no aryl is present, then the ring system is defined as a cycloalkyl if at least one non-aromatic cyclic hydrocarbon is present.

In the context of this invention alkylaryl is understood as meaning an aryl group (see above) being connected to another atom through a Ci-e-alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylaryl is understood as meaning an aryl group (see above) being connected to another atom through 1 to 4 (-CH 2 -) groups. Most preferably alkylaryl is benzyl (i.e. -Chfe-phenyl).

In the context of this invention alkylheterocyclyl is understood as meaning an heterocyclyl group being connected to another atom through a Ci- 6 -alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylheterocyclyl is understood as meaning an heterocyclyl group (see above) being connected to another atom through 1 to 4 (-CH2-) groups. Most preferably alkylheterocyclyl is -Chfe-pyridine.

In the context of this invention alkylcycloalkyl is understood as meaning an cycloalkyl group being connected to another atom through a Ci- 6 -alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylcycloalkyl is understood as meaning a cycloalkyl group (see above) being connected to another atom through 1 to 4 (-CH 2 -) groups. Most preferably alkylcycloalkyl is -CH 2 -cyclopropyl.

Preferably, the aryl is a monocyclic aryl. More preferably the aryl is a 5, 6 or 7 membered monocyclic aryl. Even more preferably the aryl is a 5 or 6 membered monocyclic aryl.

Preferably, the heteroaryl is a monocyclic heteroaryl. More preferably the heteroaryl is a 5, 6 or 7 membered monocyclic heteroaryl. Even more preferably the heteroaryl is a 5 or 6 membered monocyclic heteroaryl.

Preferably, the non-aromatic heterocyclyl is a monocyclic non-aromatic heterocyclyl. More preferably the non-aromatic heterocyclyl is a 4, 5, 6 or 7 membered monocyclic non-aromatic heterocyclyl. Even more preferably the non-aromatic heterocyclyl is a 5 or 6 membered monocyclic non-aromatic heterocyclyl.

Preferably, the cycloalkyl is a monocyclic cycloalkyl. More preferably the cycloalkyl is a 3, 4, 5, 6, 7 or 8 membered monocyclic cycloalkyl. Even more preferably the cycloalkyl is a 3, 4, 5 or 6 membered monocyclic cycloalkyl.

In connection with aryl (including alkyl-aryl), cycloalkyl (including alkyl-cycloalkyl), or heterocyclyl (including alkyl-heterocyclyl), substituted is understood - unless defined otherwise - as meaning substitution of the ring-system of the aryl or alkyl-aryl, cycloalkyl or alkyl-cycloalkyl; heterocyclyl or alkyl-heterocyclyl with one or more of halogen (F, Cl, Br, I), -Rk ,-ORk, -CN, -N0 2 , -NR k R k ·, -C(0)0R k , NR k C(0)R k · , -C(0)NR k R k' , - NR k S(0) 2 Rk' , =0, -OCH 2 CH 2 OH, -NRkC(0)NR k Rk”, -S(0) 2 NR k R k , -NRkS(0) 2 NR k Rk”, haloalkyl, haloalkoxy, -SRk, -S(0)R k , -S(0) 2 R k or C(CH3)OR k , or substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted alkylheterocyclyl, with R k, R k · and R independently being either H or a saturated or unsaturated, linear or branched, substituted or unsubstituted Ci- 6 -alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted Ci- 6 -alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted -0-Ci- 6 -alkyl (alkoxy); a saturated or unsaturated, linear or branched, substituted or unsubstituted - S-Ci- 6 -alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted -C(0)-Ci- 6 -alkyl-group; a saturated or unsaturated, linear or branched, substituted or unsubstituted -C(0)-0-Ci- 6 -alkyl-group; a substituted or unsubstituted aryl or alkyl-aryl; a substituted or unsubstituted cycloalkyl or alkyl-cycloalkyl; a substituted or unsubstituted heterocyclyl or alkyl-heterocyclyl, being R k one of Ri 4, R 21, R 31 , R 51 , R 61 , R71, Rsi, RS2 or Rs3, (being R^ one of RI 4 ·, R21’, R3i\ Rsr, Rer, R71’, Ret, R 82’ or R 83\ being Rk” one of Ri4”, R21”, R31", R51", Rei”, R71", Rsi”, R 82” or R83"; wherein R1 to R 83” and Rz are as defined in the description, and wherein when different radicals R 1 to R 83 - and R z are present simultaneously in Formula I they may be identical or different.

Most preferably in connection with aryl (including alkyl-aryl), cycloalkyl (including alkyl- cycloalkyl), or heterocyclyl (including alkyl-heterocyclyl), substituted is understood in the context of this invention that any aryl, cycloalkyl and heterocyclyl which is substituted is substituted (also in an alyklaryl, alkylcycloalkyl or alkylheterocyclyl) with one or more of halogen (F, Cl, Br, I), -R k ,-ORk, -CN , -NO2 , -NRkRk”· , NR k C(0)Rk’, - NRkS(0)2Rk· , -S(0)2NRkRk·, -NRkC(0)NRk Rk”, haloalkyl, haloalkoxy, -SRk , -S(0)Rk or S(0) 2 R k , or substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted alkylheterocyclyl, being R k one of RM , R 21 , R 31 , R 51 , Rei, R71 , Rsi, RS2 or R 83 , (being R^ one of RI 4’, R21', R31’, Rsr, Rer, R71', Rsr, R 82’ or R 83’ ; being Rk” one of RI 4 ”, R21 ·, R31”, Rsr, Rer, R71”, R 8 r, R 82 ” or R 83”; wherein R1 to Rs and R z are as defined in the description, and wherein when different radicals R 1 to Rs and R z are present simultaneously in Formula I they may be identical or different.

In connection with cycloalkyl (including alkyl-cycloalkyl), or heterocyclyl (including alkylheterocyclyl) namely non-aromatic heterocyclyl (including non-aromatic alkyl- heterocyclyl), substituted is also understood - unless defined otherwise - as meaning substitution of the ring-system of the cycloalkyl or alkyl-cycloalkyl; non-aromatic

heterocyclyl or non aromatic alkyl-heterocyclyl with V (leading to a spiro structure) and/or with =0.

A ring system is a system consisting of at least one ring of connected atoms but including also systems in which two or more rings of connected atoms are joined with “joined” meaning that the respective rings are sharing one (like a spiro structure), two or more atoms being a member or members of both joined rings.

The term “leaving group” means a molecular fragment that departs with a pair of electrons in heterolytic bond cleavage. Leaving groups can be anions or neutral molecules. Common anionic leaving groups are halides such as CI-, Br- and I-, and sulfonate esters, such as tosylate (TsO-) or mesylate.

The term“salt” is to be understood as meaning any form of the active compound used according to the invention in which it assumes an ionic form or is charged and is coupled with a counter-ion (a cation or anion) or is in solution. By this are also to be understood complexes of the active compound with other molecules and ions, in particular complexes via ionic interactions.

The term“physiologically acceptable salt" means in the context of this invention any salt that is physiologically tolerated (most of the time meaning not being toxic- especially not caused by the counter-ion) if used appropriately for a treatment especially if used on or applied to humans and/or mammals.

These physiologically acceptable salts can be formed with cations or bases and in the context of this invention is understood as meaning salts of at least one of the compounds used according to the invention - usually a (deprotonated) acid - as an anion with at least one, preferably inorganic, cation which is physiologically tolerated - especially if used on humans and/or mammals. The salts of the alkali metals and alkaline earth metals are particularly preferred, and also those with NH 4 , but in particular (mono)- or (di)sodium, (mono)- or (di)potassium, magnesium or calcium salts.

Physiologically acceptable salts can also be formed with anions or acids and in the context of this invention is understood as meaning salts of at least one of the compounds used according to the invention as the cation with at least one anion which are physiologically tolerated - especially if used on humans and/or mammals. By this is understood in particular, in the context of this invention, the salt formed with a physiologically tolerated acid, that is to say salts of the particular active compound with inorganic or organic acids which are physiologically tolerated - especially if used on humans and/or mammals. Examples of physiologically tolerated salts of particular acids are salts of: hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, formic acid, acetic acid, oxalic acid, succinic acid, malic acid, tartaric acid, mandelic acid, fumaric acid, lactic acid or citric acid.

The compounds of the invention may be present in crystalline form or in the form of free compounds like a free base or acid.

Any compound that is a solvate of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention. Methods of solvation are generally known within the art. Suitable solvates are pharmaceutically acceptable solvates. The term“solvate” according to this invention is to be understood as meaning any form of the active compound according to the invention in which this compound has attached to it via non- covalent binding another molecule (most likely a polar solvent). Especially preferred examples include hydrates and alcoholates, like methanolates or ethanolates.

Any compound that is a prodrug of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention. The term“prodrug” is used in its broadest sense and encompasses those derivatives that are converted in vivo to the compounds of the invention. Such derivatives would readily occur to those skilled in the art, and include, depending on the functional groups present in the molecule and without limitation, the following derivatives of the present compounds: esters, amino acid esters, phosphate esters, metal salts sulfonate esters, carbamates, and amides. Examples of well known methods of producing a prodrug of a given acting compound are known to those skilled in the art and can be found e.g. in Krogsgaard-Larsen et al.“Textbook of Drug design and Discovery” Taylor & Francis (April 2002).

Any compound that is a N-oxide of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention.

Unless otherwise stated, the compounds of the invention are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by 13 C- or 14 C-enriched carbon or of a nitrogen by 15 N-enriched nitrogen are within the scope of this invention. This would especially also apply to the provisos described above so that any mentioning of hydrogen or any Ή” in a formula would also cover deuterium or tritium.

The compounds of formula (I) as well as their salts or solvates of the compounds are preferably in pharmaceutically acceptable or substantially pure form. By pharmaceutically acceptable form is meant, inter alia, having a pharmaceutically acceptable level of purity excluding normal pharmaceutical additives such as diluents and carriers, and including no material considered toxic at normal dosage levels. Purity levels for the drug substance are preferably above 50%, more preferably above 70%, most preferably above 90%. In a preferred embodiment it is above 95% of the compound of formula (I), or of its salts. This applies also to its solvates or prodrugs.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

X is selected from a bond, -[C(R a R b )] P -, -[CH2] p C(0)[CH 2 ]q-, -[CH2] P C(0)N(R z )[CH2] q -, - [CH 2 ] P N(Rz)C(0)[CH 2 ] q - and -[CH 2 ] P N(R z )[CH 2 ] q -; R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl;

R b is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

X is selected from a bond, -[C(R a R b )] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R 2 )[CH 2 ] q -; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

-X-Ri is selected from -Ri, -[C(R a R b )]p-Ri, -[CH 2 ] p C(0)[CH 2 ]q-Ri, [CH 2 ] p C(0)N(Rz)[CH 2 ] q -Ri, -[CH 2 ] p N(R z )C(0)[CH 2 ] q -Ri and -[CH 2 ] p N(R z )[CH 2 ] q -Ri; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R a is selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R b is selected from hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkyny!; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R a and R b , taken together with the carbon atom to which they are attached, form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

X is selected from a bond, -[CH 2 ] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R z is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2.6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci- 6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rz is selected from hydrogen, substituted or unsubstituted C alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci- 6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein p is 0, 1 , 2, 3, 4 or 5; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

!n a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein q is O, 1 , 2, 3, 4 or 5; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein n is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Yi is— C(R-ioRio’)-; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Y 2 is— C(Rio' Rio ) ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 3 is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 3 is selected from substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 3 is selected from substituted or unsubstituted Ci-e alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 3 · is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R3' is selected from hydrogen and substituted or unsubstituted C1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 4 and R 4' are independently selected from halogen, -R 4 I , -OR 4 I , -NO2, -NR 4i R 4r , - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 41 R 4r , -NR 4i C(0)NR r R 4i ·, -SR 4 I , -S(0)R 1 , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR 4i R 4r , -OCH 2 CH 2 OR 4 I , - NR 4i S(0) 2 NR 4 rR 4t' and -C(CH3) 2 OR 4 I ; wherein R 4 I , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 4 and R 4' are independently selected from halogen, -R I , -OR 4I , -N0 2 , -NR i R 4 r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R r, -S(0) 2 NR 4I R 4I , -NR 4i C(0)NR 4r R 4i , -SR 4I , -S(0)R i , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R r, -OCH 2 CH 2 OR I , - NR 4i S(0) 2 NR 4i' R 4i” and -C(CH3) 2 OR 4I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

!n a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein

Rs, Rs·, R 5” and R 5 are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2.6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 5 and R 5 · and/or R 5 - and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs, Rs·, Rs and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs, Rs·, Rs- and Rs- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, Rs and Rs· and/or Rs- and Rs - taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R 5 , Rs·, Rs- and Rs - are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R 5 , RS·, Rs- and Rs- are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein

Rs and Re· and/or Rs- and Rs- taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs- and Rs-· taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs- and R5 " taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein

Re, Re·, Re·· and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 6 and R6· and/or Re- and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R 6 · and/or R 6 - and R 6 · taken together with the carbon atom to which they are attached may form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re, Re·, Re·· and R 6 · are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re, Re·, Re- and Re- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 -e alkynyl; alternatively, R 6 and Re· and/or R 6 - and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R6 and R6· and/or R6- and R 6 taken together with the carbon atom to which they are attached may form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R6, Re·, R6” and R · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re, Re·, Re- and R 6 are independently selected from hydrogen and substituted or unsubstituted C alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

6 and Re· and/or R 6 - and Re- taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 6 and Re' taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 6" and Re- taken together with the carbon atom to which they are attached form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 6 and Re· and/or R 6 - and Re- taken together with the carbon atom to which they are attached form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 6” and R 6 "' taken together with the carbon atom to which they are attached form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re- and Re- taken together with the carbon atom to which they are attached form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalky! and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs is selected from substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs is substituted or unsubstituted Ci-s alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re· is selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalky! and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re· is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re· is selected from hydrogen and substituted or unsubstituted C1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re and Re· taken together with the nitrogen atom to which they are attached form a substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rg and Rg· are independently selected from hydrogen, halogen, -R21, -OR21, -N0 2 , - NR 2i R 2 r, -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R 2 r, -S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 r, -SR 2 I , -S(0)R 2 I , -S(0) 2 R 2 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH 2 CH 2 OR 2 I , -NR 2i S(0) 2 NR 2i' R 2i” and -C(CH3) 2 OR 2 I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rg and Rg· are independently selected from hydrogen, halogen and -CN; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 10 and Ri 0 are independently selected from hydrogen, substituted or unsubstituted Ci. e alkyl, substituted or unsubstituted C 2- 6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, R 10 and Rio may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 10 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci- e alkyl, substituted or unsubstituted C 2- 6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R1 0 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci. 6 alkyl optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 10 and Re form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rio·· and Rio- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 - 6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rio- and R 10 - are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rio· and Rio- form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 13 and R I3 · are independently selected from hydrogen, unsubstituted Ci- 6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 13 and Ri 3' are independently selected from hydrogen and unsubstituted C 1 -6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Ri4, Rn and R^- are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 14 , Ri 4’ and R H - are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 21 , R 21' and R 21" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 21 , R 21 · and R 21 · are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 31 , R 31' and R 31" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 31 , R 31' and R 3 r are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 32 and R 32' are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 32 and R 32' are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 41 , R 41' and R 4 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 -6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 41 , R 41' and R 41” are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 51 , R 51' and R 51” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R51 , R51' and R51” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein Rei , R 61' and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R 61 , R 6 V and Rer are independently selected from hydrogen and substituted or unsubstituted Cre alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

!n a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rn, R 71 · and R 7 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2 -e alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 71 , R 71' and R 71” are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 71 is selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rei , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2.6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rei , Rsr and R 8 r are independently selected from hydrogen and substituted or unsubstituted Ci- 6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R S2 , R S2' and R 82 · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re 2 , Re 2' and R 82 - are independently selected from hydrogen and substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re 3 , Re 3' and Re 3 · are independently selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 83 , R 83' and Re 3” are independently selected from hydrogen and substituted or unsubstituted Ci-e alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Yi is— C(RioRio)-; wherein R10 and Rio are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Yi is— C(RioRio)-| wherein R10 and Rio· are independently selected from hydrogen and substituted or unsubstituted C1.6 alkyl; alternatively, R10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Y 2 is— C(Rio"Rio )-; wherein Rio- and Rur are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, Rio- and Rur may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein Y 2 is -C(Rio"Rio")-; wherein Rio- and R KT are independently selected from hydrogen and substituted or unsubstituted Ci-e alkyl; alternatively, Rio- and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen, -R21, -OR21, -NO2, -NR21R21', -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2rR2i", -SR21 , -S(0)R2i, -S(0)2R2i, -CN, haloalkyl, haloalkoxy, -C(0)OR 2I , - C(0)NR 2i R 2 r, -OCH2CH2OR21, -NR2iS(0)2NR2rR2i’’ and -C(CH3)20R2i; wherein R 21 , Riv and R 21 ·· are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein R 3 is selected from substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein, the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 3 I , halogen, -CN, ha!oa!kyl, haloalkoxy and -NR 3i R 3 r; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 3I , -OR 3I , -N0 2 , -NR 3i R 3 r, -NR 3i C(0)R 3 r, -NR 3i S(0) 2 R 3 r, -S(0) 2 NR 3i R 3 r, - NR 3i C(0)NR 3 rR 3i " , -SR 3I , -S(0)R 3I , -S(0) 2 R 3I , -CN, haloalkyl, haloalkoxy, -C(0)OR 3I , -C(0)NR 3i R 3 , -OCH 2 CH 2 OR 3I ,

NR 3i S(0) 2 NR 3i’ R 3i” and -C(CH 3 ) 2 OR 3I ;

wherein R 3I , R 3r and R 3 r are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 3' is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl; wherein, the alkyl, alkenyl or alkynyl defined in R3 , if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R 32 and R 32 are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 5 , Rs·, Rs- and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2 -e alkynyl; alternatively, R 5 and R 5 · and/or R 5 and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs- and Rs-, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R 5 -R 5' and/or R 5 -R 5" , if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -NO2, -NR51R51·, -NR 5i C(0)R 5 r, -NR 5 IS(0) 2 R51', -S(0) 2 NR 5i R 5 r, - NR 5i C(0)NR 5 rR5i”, -SR51 , -S(0)R 5i , -S(0) 2 R5i, -CN, haloalkyl, haloalkoxy, -C(0)ORsi, -C(0)NRsiRsr, -OCH 2 CH 2 OR 5I , NR 5i S(0) 2 NR 5i R5r and -C(CH 3 ) 2 OR 5I ;

wherein R 5I , Rsr and R 5 r are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Rs, Rs , Rs- and Rs- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; alternatively, Rs and Rs· and/or Rs and Rs · taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl;

wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs Rs- and Rs ·, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R5-R5' and/or Rs -Rs ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -N0 2 , -NR51R51', -NRsiC(0)Rsr, -NRsiS(0) 2 Rsr, -S(0) 2 NRsiRsi’, - NR 5I C(0)NR5I'R5I'·, -SR51 , -S(0)Rsi, -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)OR 5I , -C(0)NR 5i R5t, -OCH 2 CH 2 OR 5I ,

NR 5I S(0)2NR 5I R 5I · and -C(CH 3 ) 2 OR5i;

wherein R 51 , Rsr and R 5 r are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re, Re·, Re·· and Re · are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2.6 alkynyl; alternatively, Re and Re· and/or Re·· and Re·· taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Re and Re· and/or R 6 · and R 6 · taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in Re, Re· Re ·· and Re-, if substituted, is substituted with one or more substituent/s selected from -OR 6 I , halogen, - CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl, as defined in R 6 -R 6' and/or Re-Re·”, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 6 I , -ORei, -NO2, -NReiRer, -NReiC(0)Rer, -NR6iS(0)2R6i’, -S(0)2NR6iR6r, - NReiCfOJNRerRer, -SRei , -S(0)R 61 , -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NR6iRer, -OCH2CH2OR61,

NR 6i S(0)2NRerR6i” and -C(CH3)20R 6i ; wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R6, R6', R6” and Re- are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R 6 and R 6 · and/or R 6 - and R 6 - taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and R 6 · and/or R 6 - and Re - taken together with the carbon atom to which they are attached may form a carbonyl group; wherein the alkyl, alkenyl or alkynyl defined in R 6 , R 6 · R 6 - and R 6 , if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, - CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl, as defined in R 6 -R 6 · and/or Re-Re ", if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -OR61, -N0 2 , -NR61R6I’, -NReiC(0)Rer, -NR6iS(0) 2 Rer, -S(0) 2 NR6iR6i', - NR 6i C(0)NR6rRer, -SRei , -S(0)Rei, -S(0) 2 R 61 , -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NReiRer, -OCH 2 CH 2 OR 6 I ,

NR6iS(0) 2 NRerR6i” and -C(CH3) 2 OR6i ; wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2.6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 7 I , -OR 7 I , -NO2, - -NR 7i S(0) 2 R 7 r, -S(0) 2 NR 7i R 7 r, -S(0)R 7i , -S(0) 2 R 7i , -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR 7i R 7r , -OCH 2 CH 2 OR 7 I , NR 7i S(0) 2 NR 7i ' R 7i” and -C(CH 3 ) 2 OR 7 I ; wherein R 7 I , R 7 r and R 7 r· are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl, alkenyl or alkynyl defined in Re, if substituted, is substituted with one or more substituent/s selected from -ORei, halogen, -CN, haloalkyl, haloalkoxy and -NReiRer; wherein the cycloalkyl defined in Re, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -ORei, -NO2, -NReiRer, -NReiC(0)Rer, -NReiS(0)2Rer, -S(0)2NReiRer, - NReiC(0)NRerRei”, -SRei , -S(0)Rei, -S(0) 2 Rei, -CN, haloalkyl, haloalkoxy, -C(0)0Rei, -C(0)NReiRer, -OChbChfeORei, NReiS(0)2NRerRei” and -C(CHe)20Rei;

wherein Rei, Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein

Rs' is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl, alkenyl or alkynyl defined in R 8 ·, if substituted, is substituted with one or more substituent/s selected from -OR 8 2, halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R 8 2'; the cyclolakyl defined in R 8 ·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 2, -OR 8 2, -NO2, -NR 8 2R 8 2’, -NR 82 C(0)R 82' , -NR 82 S(0)2R82’, -S(0) 2 NR 82 R 82 ·, - NR 82 C(0)NR82'R82”, -SR82 , -S(0)Rs2, -S(0)2R82, — CN, haloalkyl, haloalkoxy, -C(0)0R 82 , -C(0)NR 82 R 82' , -0CH2CH20R 82 ,

NR 82 S(0)2NR 82' Re2” and -C(CH3) 2 OR 8 2; wherein R 8 2, Re2 and R 82 - are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Re and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; wherein the heterocyclyl, as defined in Re-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Re3, -ORe3, - NO2, -NR83R83', -NR83C(0)R83', -NR83S(0)2R83’, -S(0)2NR83R83',

NR83C(0)NR83'R83”, -SR83 , -S(0)Re3, -S(0) 2 R 83 , - CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R83', -OCH2CH2OR83,

NR83S(0)2NR83’R83” and -C(CH3)20R83; wherein Re 3 , Re 3 · and Rer are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R g and Rg· are independently selected from hydrogen, halogen, -R 2I , -OR21, -NO2, - NR21 R21 , -NR 2i C(0)R 2 r, -NR2iS(0)2R2i', -S(0)2NR2iR2r, - NR2iC(0)NR2i R2i", -SR21 , -S(0)R 2 I , -S(0) 2 R 2 I , -CN, haloalkyl, haloalkoxy, -C(0)0R 21 , -C(0)NR2iR 2 r, - OCH2CH2OR21, -NR21 S(0)2NR2i’R2i” and -C(CH3)20R2i; wherein R21, R21' and R21” are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR13, halogen, -CN, haloalkyl, haloalkoxy and -NR13R13'; wherein R13 and R I3 · are independently selected from hydrogen, unsubstituted C1-6 alkyl, unsubstituted C2-6 alkenyl, and unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -R14, -OR14, -N0 2 , -NR14R14', - NRi 4 C(0)Ri4', -NRi 4 S(0) 2 Ri4', -S(0) 2 NRi 4 Ri4', - NR 14 C(0)NRi4'Ri4”, -SRM , -S(0)Ri 4 , - S(0) 2 Ri 4 , -CN, haloalkyl, haloalkoxy, -C(0)ORI 4 , -C(0)NRi 4 Ri4·, -OCH2CH2OR14, - NRi4S(0)2NRi4'Ri4” and -C(CH3)20Ri4; wherein Ru, Ru and Ru- are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2 -e alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen, -R21, -OR21, -NO2, -NR21R21·, -NR2iC(0)R 2 r, -NR2iS(0)2R 2 r, - S(0) 2 NR 2i R 2 r, - NR 2i C(0)NR 2 rR 2 r, -SR21 , -S(0)R 2i , -S(0) 2 R2i, -CN, haloalkyl, haloalkoxy, -C(0)0R2i, -C(0)NR2iR2r, -OCH2CH2OR21, -NR2iS(0)2NR2rR2r and - C(CH 3 ) 2 OR 2I ; wherein R21, R 2 r and R21” are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR 3 I , halogen, -CN, haloalkyl, haloalkoxy and -NR 3i R 3 r; wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 3 I , -OR 3 I , -NO2, -NR 3i R 3 r, -NR 3i C(0)R 3 r, -NR 3i S(0) 2 R 3 r, -S(0) 2 NR 3i R 3 r, - NR 3i C(0)NR 3r R 3 r, -SR 3 I , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)0R3i, -C(0)NR 3i R3r, -OCH2CH2OR31 ,

NR3iS(0)2NR3tR3r and -C(CH3)20R3i;

wherein R31 , R31' and R31” are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 ·, if substituted, is substituted with one or more substituent/s selected from -OR32, halogen, -CN, haloalkyl, haloalkoxy and -NR32R32'; wherein R32 and R32- are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 5 , Rs· Rs and Rs···, if substituted, is substituted with one or more substituent/s selected from -OR51, halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr;

wherein the cycloalkyl, as defined in R5-R5· and/or Rs-Rs ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R51, -OR51, -NO2, -NR51R51·, -NR 5i C(0)R 5 r, -NR 5I S(0) 2 R 5I , -S(0) 2 NR 5i R5r, - NR5iC(0)NR 5 rR5i”, -SR51 , -S(0)R 5i , -S(0) 2 R 5i , -CN, haloalkyl, haloalkoxy, -C(0)0R 5i , -C(0)NR 5i R 5 r, -OCH 2 CH 2 OR 5I , NR 5i S(0) 2 NR 5 rR 5 r and -C(CH 3 ) 2 OR 5I ;

wherein R51 , Rsr and R 5 I · are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2- e alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re·· and Re···, if substituted, is substituted with one or more substituent/s selected from -OR61, halogen, - CN, haloalkyl, haloalkoxy and -NReiRer;

wherein the cycloalkyl, as defined in R 6 -R 6 · and/or Re-Re··, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rei, -ORei, -N0 2 , -NReiRer, -NR 6i C(0)Rer, -NR 6I S(0) 2 R 6I ·, -S(0) 2 NR 6i R 6i ·, - NReiC(0)NRerR6i ", -SRei , -S(0)Rei, -S(0) 2 R 6i , -CN, haloalkyl, haloalkoxy, -C(0)0Rei , -C(0)NR6iR6r, -OCH 2 CH 2 OR 6 I ,

NReiS(0) 2 NRerRei" and -C(CH3)20R6i ; wherein R 6 I , R 6 r and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R 71 , -OR 71 , -NO 2 , -

NR71R71·, -NR 7i C(0)R 7 r, -NR7iS(0) 2 R 7 r, -S(0) 2 NR 7i R7r,

NR 71 C(0)NR 7 rR 7 r, -SR71 , -S(0)R 7i , -S(0) 2 R 7i , -CN, haloalkyl, haloalkoxy, -C(0)0R 7i , -C(0)NR7iR 7 r, -OCH2CH2OR71,

NR7iS(0) 2 NR 7 rR7r' and -C(CH 3 ) 2 OR 7 I ; wherein R 71 , R 7 r and R 71” are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 8 , if substituted, is substituted with one or more substituent/s selected from -OR 8 I , halogen, -CN, haloalkyl, haloalkoxy and -NR 8 I R 8 I·; wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 I , -OR 8 I , -NO2, -NR 8i R 8 r, -NR 8i C(0)R 8 r, -NR 8i S(0)2R 8 r, -S(0)2NR 8i R 8 r, - NR 8i C(0)NR 8 rR8i”, -SR 8 I , -S(0)R 8 I , -S(0)2RSI , - CN, haloalkyl, haloalkoxy, -C(0)0R 8i , -C(0)NR 8i R 8r , -OCH 2 CH 2 OR 8 I ,

NR 8i S(0)2NR 8 rR 8i ” and -C(CH 8 )20R 8 I ; wherein R 8I , R 8 r and Rsr are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2.6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 8 ·, if substituted, is substituted with one or more substituent/s selected from -OR 8 2, halogen, -CN, haloalkyl, haloalkoxy and -NR 8 2R 8 2'; the cyclolakyl defined in R 8 ·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 2, -OR 82I -NO2, -NR 8 2R 8 2', -NR 8 2C(0)R 8 2 , -NRS2S(0)2R 82' , -S(0) 2 NR 82 RS2', - NR 82 C(0)NR 82’ R 82 ”, -SR 82 , -S(0)R 82 , -S(0) 2 R 82 , — CN, haloalkyl, haloalkoxy, -C(0)0R 82 , -C(0)NR 82 R 82 ·, -OCH 2 CH 2 OR 82 ,

NR 82 S(0)2NR 8 2'R 8 2" and -C(CH3)20R 82 ; wherein R 82 , R 8 2· and R 8 2· are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein wherein the heterocyclyl, as defined in R 8 -R 8 ·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 3, -OR 8 3, - NO2, -NR 83 R 83’ , -NR 83 C(0)R 83' , -NR 83 S(0)2R83’, -S(0) 2 NR 83 R 83' ,

NR 83 C(0)NR 83' R 83 " , -SR 83 , -S(0)R 83 , -S(0) 2 R 83 , — CN, haloalkyl, haloalkoxy, -C(0)0R 83 , -C(0)NR 83 R 83' , -OCH2CH 2 OR 83 ,

NR 83 S(0) 2 NR 83 R 83" and -C(CH3)20R 83 ; wherein R 83 , R 8 3 and R 83 - are independently selected from hydrogen, substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR 13 , halogen, -CN, haloalkyl, haloalkoxy and -NR 13 R 13' ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding sait thereof, or a corresponding soivate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, -OR13, halogen, -CN, haloalkyl, haloalkoxy and -NR13R13'; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein the aryl, heterocyclyl or cycloalkyl, also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from =0, halogen, -Ru, -OR14, -NO2, -NRi 4 Ri 4' , - NRi 4 C(0)Ri4·, -NRi 4 S(0) 2 Ri4·, -S(0) 2 NRi 4 Ri4 , - NRi 4 C(0)NRi 4 -Ri4··, -SRM , -S(0)Ri 4 , - S(0) 2 Ri4, -CN, haloalkyl, haloalkoxy, -C(0)0Ri 4 , -C(0)NRI 4 RI 4 ·, -OCH 2 CH 2 ORI 4 , - NRi 4 S(0) 2 NRi4'Ri4" and -C(CH3) 2 ORi4! optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen, -R21 , -OR 2I , -N0 2 , -NR 2i R 2r , -NR 2i C(0)R 2 r, -NR 2i S(0) 2 R 2r , - S(0) 2 NR 2i R 2 , - NR 2i C(0)NR 2 rR 2i” , -SR 2 I , -S(0)R 2i , -S(0) 2 R 2i , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, -OCH 2 CH 2 OR 2I , -NR 2i S(0) 2 NR 2 rR 2i” and - C(CH 3 ) 2 OR 2 I; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl in R 2 , if substituted, is substituted with one or more substituent/s selected from halogen and -CN; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s selected from -OR31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31 R31'; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R3, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from -OR31 , halogen, -CN, haloalkyl, haloalkoxy and -NR31 R31'; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 , if substituted, is substituted with one or more substituent/s of halogen·; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s of halogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl in R3, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R31 , -OR31, -NO2, -NR31R31', -NR 3i C(0)R 3 r, - NR 3i S(0) 2 R 3 r, -S(0) 2 NR 3 IR31', - NR3iC(0)NR 3 rR 3 r, -SR31 , -S(0)R 3i , -S(0) 2 R 3i , -CN, haloalkyl, haloalkoxy, -C(0)0R3i, -C(0)NR3iR3r, -OCH 2 CH 2 OR3i, -NR3iS(0) 2 NR3i R3r and -C(CH 3 ) 2 OR 3 I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein wherein the cycloalkyl in R 3 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected -R 31 , -OR 31 , halogen, - CN, haloalkyl, haloalkoxy and -NR31R31·; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 3 ·, if substituted, is substituted with one or more substituent/s selected from -OR 32 , halogen, -CN, haloalkyl, haloalkoxy and -NR 32 R 32 ·; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 5 , R 5 · Rs- and R5-, if substituted, is substituted with one or more substituent/s selected from -OR 51 , halogen, - CN, haloalkyl, haloalkoxy and -NRsiRsr; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl, as defined in R 5 -R 5' and/or Rs-Rs”, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 51 , -OR 51 , -NO 2 , -NR51R51', - NR 5i C(0)Rsr, -NR 5i S(0) 2 R 5 r, -S(0) 2 NR 5i R 5 r, - NR 5i C(0)NR 5 rR 5i , -SR51 , -S(0)R 5i , - S(0) 2 RSI , -CN, haloalkyl, haloalkoxy, -C(0)0R 5i , -C(0)NR 5 IR 5 I·, -OCH 2 CH 2 OR 5 I, - NR 5i S(0) 2 NR 5 rR5r and -C(CH 3 ) 2 OR 5I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl, as defined in R 5 -R 5' and/or Rs-Rs- , if substituted, is substituted with one or more substituent/s selected from selected from -R 51 , -OR 51 , halogen, -CN, haloalkyl, haloalkoxy and -NRsiRsr; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 6 , Re· Re- and Re-, if substituted, is substituted with one or more substituent/s selected from -OR61, halogen, -CN, haloalkyl, haloalkoxy and - R6iR6i·; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl, as defined in Re-Re· and/or Re-Re-, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 6 I , -ORei, -NO2, - NReiRer, -NR6iC(0)Rer, -NR6iS(0) 2 Rer, -S(0) 2 NR6iRer, - NR6iC(0)NRerR6r’, - SRei , -S(0)Rei, -S(0) 2 R 6i , -CN, haloalkyl, haloalkoxy, -C(0)ORei, - C(0)NReiRer, -OCH 2 CH 2 ORei, -NR6iS(0) 2 NRevRei·· and -C(CH 3 ) 2 ORei; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl, as defined in R 6 -R 6' and/or Re-Re ··, if substituted, is substituted with one or more substituent/s selected from halogen, -R 6 I , - ORei, -NReiRer, -CN, haloalkyl, haloalkoxy; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s selected from halogen, -R71, -OR71, -NO2, - NR71R71·, -NR 7i C(0)R 7i' , -NR 7i S(0) 2 R 7 r, -S(0) 2 NR 7i R7r,

NR7iC(0)NR 7i' R 7i " , -SR71 , -S(0)R 7I , -S(0) 2 R 7I , -CN, haloalkyl, haloalkoxy, -C(0)OR 7I , -C(0)NR 7i R 7 r, -OCH 2 CH 2 OR 7I ,

NR 7i S(0) 2 NR 7 rR7r and -C(CH 3 ) 2 OR 7I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the aryl or heterocyclyl, as defined in R 7 , if substituted, is substituted with one or more substituent/s of halogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in Re, if substituted, is substituted with one or more substituent/s selected from -OR 8 I , halogen, -CN, haloalkyl, haloalkoxy and -NReiRer; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from -OR 8 I , halogen, -CN, haloalkyl, haloalkoxy and -NRsiRsr; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding sait thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -R 8 I , -OR 8 I , -NO2, -NR 8i R 8 r, -NR 8i C(0)R 8 r, -NR 8i S(0)2R 8 r, -S(0)2NR 8i R 8 r, - NR 8i C(0)NR 8i R 8 r’, -SR 8 I , -S(0)R 8 I , -S(0)2RSI , - CN, haloalkyl, haloalkoxy, -C(0)0R 8i , -C(0)NR 8i R 8r , -OCH 2 CH 2 OR 8 I ,

NR 8i S(0)2NR 8 rR 8 r and -C(CH 3 ) 2 0R 8 I ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cycloalkyl defined in R 8 , also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from halogen, -R 8 I , - OR 8 I , -NRsiRsr, -CN, haloalkyl and haloalkoxy; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from - ORS 2 , halogen, -CN, haloalkyl, haloalkoxy and -NR 82 RB2'; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the alkyl, alkenyl or alkynyl defined in Re·, if substituted, is substituted with one or more substituent/s selected from -ORs 2 , halogen, -CN, haloalkyl, haloalkoxy and -NR 82 R82·; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cyclolakyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rs2, -OR82, -NO2, -NR82R82’, -NR82C(0)R82’, -NR82S(0)2R82’, -S(0)2NR82Re2’, - NR82C(0)NR82 R82”, -SR82 , -S(0)Re2, -S(0) 2 R 82 , -CN, haloalkyl, haloalkoxy, -C(0)ORe2, -C(0)NR82R82·, -OCH2CH2OR82,

NR82S(0)2NR82’R82·' and -C(CH 3 )20R 82 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein the cyclolakyl defined in Re·, also in alkylcycloalkyl, if substituted, is substituted with one or more substituent/s selected from halogen, -Rs 2 , - OR S2 , -NR 82 R 82' , -CN, haloalkyl and haloalkoxy; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein wherein the heterocyclyl, as defined in Re-Re·, if substituted, is substituted with one or more substituent/s selected from =0, halogen, -Rs 3 , -ORs 3 , - NO2, -NR83R83’, -NR83C(0)R83’, -NR83S(0)2R83’, -S(0)2NR83R83’,

NR83C(0)NR83’R83 m , -SR83 , -S(0)Re3, -S(0) 2 R 83 , - CN, haloalkyl, haloalkoxy, -C(0)ORe3, -C(0)NR 83 R83·, -OCH2CH2OR83,

NR83S(0)2NR83’R83” 3nd -C(CH3)20Re3; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

!n a further embodiment the compound according to the invention of genera! Formula (I) is a compound wherein any cycloalkyl, also in alkylcycloalkyl, if substituted and the substitution has not been defined otherwise, it is substituted with one or more substituent/s selected from -R 14 , - OR 14 , halogen, -CN, haloalkyl, haloalkoxy and -NR 14 R 14' optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in an mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

X is a bond, -[C(R a R b )] P -, -[C(R a R b )] p C(0)[C(R c Rd)]q-, -[C(R a R b )]pC(0)N(R z )[C(R c Rd)] q - , -[C(R a R b )]pN(R z )C(0)[C(R c Rd)]q- or -[C(R a R b )] p N(R z )[C(R c Rd)] q -;

R z is selected from hydrogen, substituted or unsubstituted C alkyl, substituted or unsubstituted C 2.6 alkenyl, substituted or unsubstituted C 2.6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl;

R a is selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; R b is selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; alternatively, R a and R b , taken together with the carbon atom to which they are attached, may form a substituted or unsubstituted cycloalkyl;

R c is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl;

R d is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

X is a bond, - -[C(R a Rb)]pN( optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R z is selected from hydrogen, substituted or unsubstituted C 1 -6 alkyl, substituted or unsubstituted C 2.6 alkenyl, substituted or unsubstituted C 2 -6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and - C(0)-Ci- 6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein R a is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

Rb is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein R a and R b , taken together with the carbon atom to which they are attached, form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein R c is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R d is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein X is selected from a bond, -[CH 2 ] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -; preferably X is selected from a bond, -[CH 2 ] p -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ]pN(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -; more preferably bond or a substituted or unsubstituted group selected from -CH 2 -, -CH 2 CH 2 - , C(O), -CH 2 C(0)-, -CH 2 CH 2 C(0)-, -NHC(0)CH 2 - and NHC(0)CH 2 CH 2 -; and/or

Ri is and/or

R z is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2- e alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci- 6 alkyl; preferably R z is selected from hydrogen; and/or p is 0, 1 , 2, 3, 4 or 5; preferably p is 0, 1 or 2; and/or q is 0, 1 , 2, 3, 4 or 5; preferably q is 0 or 1 ; and/or

Yi is -C(RioRio )-; preferably Yi is -CH 2 -; and/or Y2 is -C(RioRio·)-; preferably and/or n is 0 or 1 ; and/or m is O or l ; and/or r is 0 or 1 ; and/or t is 0 or 1 ;

and/or

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, preferably R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl, more preferably R 2 is a substituted or unsubstituted group selected from phenyl and thiophen; and/or

R 3 is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;preferably R 3 is substituted or unsubstituted C 1-6 alkyl; more preferably R 3 is substituted or unsubstituted methyl or substituted or unsubstituted ethyl; and/or

R 3' is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R 3 is hydrogen or substituted or unsubstituted methyl; and/or

R 4 and RA· are independently selected from halogen, -R 4 I , -OR 4I , -N0 2 , -NR 4i R 4 r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 , -S(0) 2 NR 4i R 4 , -NR 4i C(0)NR 4r R 4r , -SR 4 I , -S(0)R 41 , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4I R 4I , -OCH 2 CH 2 OR 4 I , - NR 4i S(0) 2 NR 4 rR 4 r and -C(CH 3 ) 2 OR 4 I ; preferably R 4 and R 4 · are both hydrogen; and/or

Rs, Rs·, Rs- and Rs · are independently selected from hydrogen, halogen, substituted or unsubstituted C alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably Rs, Rs·, Rs- and Rs · are all hydrogen; alternatively, Rs and Rs· and/or Rs- and Rs taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl and/or

Re, Re·, Re· and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R 6 , Re·, R 6 and R 6 are all hydrogen; alternatively, R 6 and R 6 · and/or R 6 - and R 6 taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, R 6 and Rs· and/or Re- and R 6 · taken together with the carbon atom to which they are attached may form a carbonyl group; and/or R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; preferably R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl; more preferably R 7 is selected from substituted or unsubstituted phenyl and substituted or unsubstituted pyridine and substituted or unsubstituted thiophen;

and/or

Re is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Re is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl; and/or

Re· is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Re· is selected from hydrogen and substituted or unsubstituted methyl; and/or

Ra and Ra· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; and/or

Rg and Rg· are independently selected from hydrogen, halogen, -R21, -OR21, -NO2, - NR21R21', -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2rR2r, -SR21 , -S(0)R 2 I , -S(0) 2 R 2 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 2 I , -C(0)NR 2i R 2 r, - OCH2CH2OR21, -NR2iS(0)2NR2i'R2r and -C(CH3)20R2i; preferably Rg and Rg· are selected from hydrogen, halogen and -CN; more preferably Rg and Rg· are selected from hydrogen, fluorine and -CN; and/or R 10 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci- e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; preferably R 10 and Rio are both hydrogen; alternatively, R 10 and R 10 may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

and/or

Rio·· and Rio- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 - 6 alkynyl; preferably Rio- and Rio- are both hydrogen; alternatively, Rio- and R 10 - may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; preferably Rio- and Rio- form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl;

and/or

R 13 and RI 3 · are independently selected from hydrogen, unsubstituted C 1.6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl; and/or

R 14 , Ri b and Rn- are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; and/or

R 21 , R 21 ' and R 21 · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 -6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; and/or R 31 , R 31 ' and R 3 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; and/or

R 32 and R 32' are independently selected from hydrogen, substituted or unsubstituted Ci- e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; and/or

R 41 , R 4 r and R 41" are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R 41 is hydrogen; and/or

R 51 , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

and/or

R 6i , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; and/or

R 71 , R 71 ' and R 71" are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R 71 is hydrogen; and/or Rei, Rer and R 8 r are independently selected from hydrogen, substituted or unsubstituted Ci-a alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; and/or RS2, RS2' and Ra2 are independently selected from hydrogen, substituted or unsubstituted Ci-a alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; and/or

RS3, RS3' and Ra3· are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

X is selected from a bond, -[CH 2 ] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(Rz)C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -; preferably X is selected from a bond,

-[CH 2 ] p -, -[CH 2 ] p C(0)[CH 2 ] q -, -[CH 2 ] p N(R z )C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -; more preferably bond or a substituted or unsubstituted group selected from -CH 2 -, -CH 2 CH 2 - , C(O), -CH 2 C(0)-, -CH 2 CH 2 C(0)-, -NHC(0)CH 2 - and NHC(0)CH 2 CH 2 -; if X is selected from a bond, -[CH 2 ] p -, -[CH 2 ] p C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )C(0)[CH 2 ] q -, q is 0, 1 , 2, 3, 4 or 5; preferably q is 0, 1 or 2; and if X is selected from -[CH 2 ] p C(0)N(R z )[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -, q is 1 , 2, 3, 4 or 5; preferably q is 1 or 2; and/or

and/or

R z is selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci- 6 alkyl; preferably R z is selected from hydrogen; and/or p is 0, 1 , 2, 3, 4 or 5; preferably p is 0, 1 or 2; and/or q is 0, 1 , 2, 3, 4 or 5; preferably q is 0 or 1 ; and/or

Yi is -C(RioRio·)-; preferably Y1 is -CH2-; and/or

Y2 is -C(RioRio )-; preferably and/or n is 0 or 1 ; and/or m is 0 or 1 ; and/or r is 0 or 1 ; and/or t is 0 or 1 ;

and/or R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, preferably R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl, more preferably R 2 is a substituted or unsubstituted group selected from phenyl and thiophen; and/or R 3 is selected from substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;preferably R 3 is substituted or unsubstituted C 1-6 alkyl; more preferably R 3 is substituted or unsubstituted methyl or substituted or unsubstituted ethyl; and/or

R 3 is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2- e alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R 3' is hydrogen or substituted or unsubstituted methyl; and/or R 4 and R · are independently selected from halogen, -R 4 I , -OR 4 I, -N0 2 , -NR 4i R r, - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 4i R 4r , -NR 4i C(0)NR 4r R r, -SR 4 I , -S(0)R 4i , - S(0) 2 R 4 I , -CN, haloalkyl, haloalkoxy, -C(0)OR 4 I , -C(0)NR 41 R 4 r, -OCH 2 CH 2 OR 41 , - NR 4 IS(0) 2 NR I'R 4 I - and -C(CH 3 ) 2 OR I ; preferably R and R 4 · are both hydrogen; and/or

R5, Rs·, Rs- and Rs·· are independently selected from hydrogen, halogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably Rs, Rs·, Rs- and Rs - are all hydrogen; alternatively, Rs and Rs· and/or Rs- and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl and/or

Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci-s alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2- e alkynyl; preferably Re, Re·, Re- and Re- are all hydrogen; - alternatively, R 6 and R 6 · and/or R 6 · and Rs- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; alternatively, Rs and R 6 · and/or R 6 - and Rs - taken together with the carbon atom to which they are attached may form a carbonyl group; and/or

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; preferably R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted aromatic heterocyclyl; more preferably R 7 is selected from substituted or unsubstituted phenyl and substituted or unsubstituted pyridine and substituted or unsubstituted thiophen;

and/or Re is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Re is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl; and/or

Re· is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Re· is selected from hydrogen and substituted or unsubstituted methyl; and/or

Re and Re· taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; and/or

Rg and Rg· are independently selected from hydrogen, halogen, -R21, -OR21, -N0 2 , - NR21R21·, -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2i R2i”, -SR21 , -S(0)R 2 I , -S(0) 2 R 21 , -CN, haloalkyl, haloalkoxy, -C(0)OR 2 I , -C(0)NR 2i R 2 r, - OCH2CH2OR21, -NR2iS(0)2NR 2 rR2i " and -C(CH 3 )20R2i; preferably Rg and Rg· are selected from hydrogen, halogen and -CN; more preferably Rg and Rg· are selected from hydrogen, fluorine and -CN; and/or

R10 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci- e alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; preferably R10 and R^ are both hydrogen; alternatively, R 10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl;

and/or Rio- and Rio- are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2 - e alkynyl; preferably R io ·· and Rio- are both hydrogen; alternatively, Rio- and Rio- may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; preferably Rio · and Rio- form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl;

and/or

R 13 and Ri 3' are independently selected from hydrogen, unsubstituted C 1 -6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl; and/or

R 14 , Ri 4’ and R 14 are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; and/or

R 21 , R 21’ and R 21 · are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; and/or

R 31 , R 31 ' and R 31 " are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; and/or

R 32 and R 32 are independently selected from hydrogen, substituted or unsubstituted Ci. 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; and/or

R41 , R 4 r and R41 " are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-8 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R41 is hydrogen; and/or

R51 , Rsr and Rsr are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

and/or

R 61 , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; and/or

R71 , R71' and R71” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 -6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R71 is hydrogen; and/or

Rei , Rsr and R 8 r are independently selected from hydrogen, substituted or unsubstituted Ci -8 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; and/or

R 82 , Re and R 82” are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2- 6 alkynyl; and/or RS3, Re3' and R83- are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is selected from a bond, -[CH 2 ] P -, -[CH 2 ]pC(0)[CH 2 ]q-, -[CH 2 ] p C(0)N(R z )[CH 2 ] q -, - [CH 2 ] p N(R z )C(0)[CH 2 ]q- and -[CH 2 ] p N(R z )[CH 2 ] q -; and/or p is 0, 1 , 2, 3, 4 or 5; and/or q is 0, 1 , 2, 3, 4 or 5; and/or n is 0 or 1 ;

and/or

Yi is -C(RioRio )-; and/or

Y 2 is— C(Rio'Rio ) ! and/or Ri is and/or m is 0, 1 or 2; and/or r is 0, 1 or 2;

and/or t is 0, 1 , 2, 3, 4 or 5; and/or R z is selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci- 6 alkyl; wherein the alkyl is C1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or

2-methylpropyl; and/or the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2 -6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; and/or

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, wherein the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; preferably the aryl is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazoie, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; preferably the heterocyclyl is thiophen; and/or

R 3 is selected from substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein

the alkyl is C1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the Ci- 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C1-6 alkyl is methyl or ethyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

and/or

R 3' is selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl;

wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

and/or

R 4 and R 4 are independently selected from halogen, -R 4 I , -OR 4 I, -NO2, -NR 4i R 4 r, - NR 4i C(0)R 4r , -NR 4i S(0) 2 R 4 r, -S(0) 2 NR 41 R 4r , -NR 4i C(0)NR 4 rR 4r , -SR 41 , -S(0)R 4i , - S(0) 2 R 4I , -CN, haloalkyl, haloalkoxy, -C(0)0R 4i , -C(0)NR 4i R 4r , -OCH 2 CH 2 OR 4 I , - NR 4 IS(0) 2 NR 4 I R 4 I and -C(CH 3 ) 2 OR 4 I ; wherein

the alkyl is C 1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl;

and/or

R 5 , R 5 , R 5 ” and R 5 ”' are independently selected from hydrogen, halogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2- e alkenyl and substituted or unsubstituted C 2-6 alkynyl; wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; alternatively, R 5 and R 5 · and/or R 5” and R 5 taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; wherein the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

and/or

Re, Re·, Re- and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; alternatively, Re and R 6 · and/or Re·· and Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; wherein

the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; alternatively, Re and Re· and/or Re- and R 6 · taken together with the carbon atom to which they are attached may form a carbonyl group;

and/or

R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

Wherein the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; preferably the aryl is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5- thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; preferably the heterocyclyl is pyridine or thiophen;

and/or

Re is selected from substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl is C1.6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C1-6 alkyl is methyl or ethyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

and/or

Rs is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, substituted or unsubstituted C 2 -e alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; wherein the alkyl is C 1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

and/or

Rg and Rg· are independently selected from hydrogen, halogen, -R21, -OR21, -NO2, - NR21R21’, -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2i’R2i”, -SR21 , -S(0)R 21 , -S(0) 2 R 21 , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH2CH2OR21, -NR 2i S(0) 2 NR 2 rR2r and -C(CH 3 ) 2 OR 2 I; wherein the alkyl is C 1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2- methyl propyl; and/or

R1 0 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2- 6 alkenyl and substituted or unsubstituted C 2 -e alkynyl; wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

alternatively, R 10 and Rio· may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; wherein the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; and/or

R 10 - and Ri<r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl; wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

alternatively, Rio- and Rur form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; wherein

the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; preferably the cycloalkyl is cyclopropyl; and/or

R 13 and RI 3 · are independently selected from hydrogen, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl;

wherein the Ci-ealkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

R 14 , R I4 · and Ru- are independently selected from hydrogen, unsubstituted Ci-s alkyl, unsubstituted C 2 -e alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; and/or the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5- thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; and/or

R 21 , R 21' and R 21” are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein

the Ci. 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the C 1-6 alkyl is methyl, ethyl or propyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

and/or

R31, R31' and R31" are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C 2 -6 alkynyl; wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methyl propyl; and/or the C 2 -6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

and/or

R32 and R32' are independently selected from hydrogen, substituted or unsubstituted Ci-6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

and/or

R41 , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2 -e alkenyl and substituted or unsubstituted C2-6 alkynyl; wherein

the Ci- 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

R 51 , Rsr and R 51" are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

and/or

R 61 , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; wherein the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

R 71 , R 71' and R 7 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably, the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

Rei, Rer and R 8 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

RS2, RS 2 · and R 82” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

wherein

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or

R83, S 3' and R 83” are independently selected from hydrogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl;

wherein the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R z as defined in any of the embodiments of the present invention, the alkyl is Ci- 6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 2 as defined in any of the embodiments of the present invention, the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; preferably the aryl is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5- thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; preferably the heterocyclyl is thiophen;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R3 as defined in any of the embodiments of the present invention, the alkyl is C1.6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C1-6 alkyl is methyl or ethyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 3' as defined in any of the embodiments of the present invention, the C 1.6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 4 and R 4 · as defined in any of the embodiments of the present invention, the alkyl is Ci -6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rs, Rs·, Rs·· and Rs - as defined in any of the embodiments of the present invention, the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 5 , Rs·, Rs· and Rs- as defined in any of the embodiments of the present invention, the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 6 , R 6 ·, R 6 - and Re- as defined in any of the embodiments of the present invention, the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 6 , !¾', R 6 - and Re- as defined in any of the embodiments of the present invention, the cycloalkyl is C3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 7 as defined in any of the embodiments of the present invention, the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; preferably the aryl is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5- thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole; preferably the heterocyclyl is pyridine or thiophen;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rs as defined in any of the embodiments of the present invention, the alkyl is Ci_ 6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the C1-6 alkyl is methyl or ethyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rs as defined in any of the embodiments of the present invention, the alkyl is C 1-6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the Ci_ 6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2 -e -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rg and Rg as defined in any of the embodiments of the present invention, the alkyl is Ci- 6 alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2- methylpropyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 10 and Rio as defined in any of the embodiments of the present invention, the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 10 and R^ as defined in any of the embodiments of the present invention, the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rio- and R 10 as defined in any of the embodiments of the present invention, the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 10 · and Rio- as defined in any of the embodiments of the present invention, the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C 3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; preferably the cycloalkyl is cyclopropyl;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 13 and Ri 3 as defined in any of the embodiments of the present invention, the Ci-ealkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R14, RH· and R14 as defined in any of the embodiments of the present invention, the Ci-6alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; and/or the cycloalkyl is C 3-8 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C 3-7 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C3-6 cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; and/or the aryl is selected from phenyl, naphthyl, or anthracene; preferably is naphthyl and phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms selected from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from oxazepan, pyrrolidine, imidazole, oxadiazole, tetrazole, azetidine, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyran, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, quinolone, isoquinoline, tetrahydrothienopyridine, phthalazine, benzo-1 ,2,5- thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, benzodioxolane, benzodioxane, carbazole, oxaspirodecan or thiazole;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R21, R 2 r and R21 as defined in any of the embodiments of the present invention,

the C1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the C1-6 alkyl is methyl, ethyl or propyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R31 , R 3 r and R 3 r as defined in any of the embodiments of the present invention,

the Ci-ealkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 32 and R 32 · as defined in any of the embodiments of the present invention,

the Ci- 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 4I , R 4 r and R 4 r as defined in any of the embodiments of the present invention,

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the Ci -6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 51 , Rsr and Rsr as defined in any of the embodiments of the present invention,

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 61 , R 6 r and Rer as defined in any of the embodiments of the present invention, the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl, more preferably the C 1-6 alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 71 , R 7 r and R 7 r as defined in any of the embodiments of the present invention,

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; preferably the Ci-e alkyl is methyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in Rei, Rer and Rer as defined in any of the embodiments of the present invention,

the Ci- 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 82 , R 82 · and R 82 · as defined in any of the embodiments of the present invention,

the Ci- 6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C 2-6 -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R 83 , Re3' and R 83 · as defined in any of the embodiments of the present invention,

the C 1-6 alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl, or 2-methylpropyl; and/or the C 2-6 -alkenyl is preferably selected from ethylene, propylene, butylene, pentylene, hexylene, isopropylene and isobutylene; and/or the C -alkynyl is preferably selected from ethyne, propyne, butyne, pentyne, hexyne, isopropyne and isobutyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein p is 0, 1 , 2, 3, 4 or 5; preferably p is 0, 1 or 2; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein q is 0, 1 , 2, 3, 4 or 5; preferably q is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein n is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein m is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein r is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein t is 0 or 1 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

X is selected from a X is selected from a bond, -[CH 2 ] P -, -[CH 2 ] P C(0)[CH2]q-, - [CH 2 ] p C(0)N(R z )[CH 2 ]q-, -[CH 2 ]pN(Rz)C(0)[CH 2 ] q - and -[CH 2 ] p N(R z )[CH 2 ] q -; preferably X is selected from a bond, -[CH 2 ] P -, -[CH 2 ] p C(0)[CH 2 ] q -, -[CH 2 ] p N(R z )C(0)[CH 2 ]q- and - [CH 2 ] p N(Rz)[CH 2 ]q-; more preferably bond or a substituted or unsubstituted group selected from -CH 2 -, -CH 2 CH 2 - , C(O), -CH 2 C(0)-, -CH 2 CH 2 C(0)-, -NHC(0)CH 2 - and NHC(0)CH 2 CH 2 -; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Yi is -C(RioRio')-; preferably Yi is -CH 2 -; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Y 2 is -C(RioRio')-; preferably optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R z is selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl and -C(0)-Ci-e alkyl; preferably R z is selected from hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 2 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl, preferably R 2 is a substituted or unsubstituted group selected from phenyl and thienyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (!) the compound is a compound, wherein

R 3 is selected from substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl;preferably R 3 is substituted or unsubstituted C 1-6 alkyl; more preferably R 3 is substituted or unsubstituted methyl or substituted or unsubstituted ethyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 3' is selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R 3' is hydrogen or substituted or unsubstituted methyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 4 and R 4' are independently selected from halogen, -R41, -OR41, -NO2, -NR41R41', - NR 4i C(0)R 4 r, -NR 4i S(0) 2 R 4 r, -S(0) 2 NR4iR4r, -NR4iC(0)NR 4 rR 4 r, -SR41 , -S(0)R 4i , - S(0) 2 R 4i , -CN, haloalkyl, haloalkoxy, -C(0)OR4i, -C(0)NR 4i R4r, -OCH2CH2OR41, - NR4iS(0)2 R4rR4i” and -C(CH3)20R4i; wherein R 41 , R 4 r and R 4 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R 41 is hydrogen; preferably R 4 and R 4 · are both hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Rs, Rs , R 5" and Rs- are independently selected from hydrogen, halogen, substituted or unsubstituted C 1.6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; R 5 , Rs·, Rs and R 5 - are all hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein Re, R 6' , R 6" and Re- are independently selected from hydrogen, halogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R 6 , R 6 ·, R 6 - and Re- are all hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding soivate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 6 , R 6' and/or R 6 , Re- taken together with the carbon atom to which they are attached may form a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Re and R 6 · and/or Re- and Re- taken together with the carbon atom to which they are attached form a carbonyl group; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein R 7 is selected from substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; preferably R 7 is selected from substituted or unsubstituted phenyl and substituted or unsubstituted pyridinyl and substituted or unsubstituted thienyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Re is selected from substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Rs is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Rs is selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C2-6 alkenyl, substituted or unsubstituted C2-6 alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted alkylcycloalkyl; preferably Re· is selected from hydrogen and substituted or unsubstituted methyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Re and R 8 · taken together with the nitrogen atom to which they are attached may form a substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Rg and Rg· are independently selected from hydrogen, halogen, -R21, -OR21, -NO2, - NR21R21', -NR 2i C(0)R 2 r, -NR2iS(0)2R2r, -S(0)2NR2iR2r, - NR2iC(0)NR2rR2i'', -SR21 , -S(0)R 2 I , -S(0) 2 R 2i , -CN, haloalkyl, haloalkoxy, -C(0)0R 2i , -C(0)NR 2i R 2 r, - OCH2CH2OR21, -NR 2i S(0) 2 NR 2 rR 2i ·' and -C(CH 3 )20R2i; preferably Rg and Rg· are selected from hydrogen, halogen and -CN; more preferably Rg and Rg· are selected from hydrogen, fluorine and -CN; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R10 and Rio are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; preferably R10 and Rio are both hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R10 and Re form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Rio· and Rio- are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2- e alkynyl; preferably Rio- and Rio- are both hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein Rio · and R 10 - may form, with the carbon atom to which they are attached, a substituted or unsubstituted cycloalkyl; preferably R KT and R 10 ' form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 13 and R I3 · are independently selected from hydrogen, unsubstituted Ci-e alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 14 , R M' and R 14 are independently selected from hydrogen, unsubstituted C1. 6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R21 , R21 ' and R 2 r are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R31 , R31' and R31” are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R32 and R32' are independently selected from hydrogen, substituted or unsubstituted Ci- 6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R41 , R41 ' and R41 " are independently selected from hydrogen, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; preferably R41 is hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R51 , R51 ' and Rsr are independently selected from hydrogen, substituted or unsubstituted C1.6 alkyl, substituted or unsubstituted C2-6 alkenyl, and substituted or unsubstituted C2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein R 6 I , Rer and Rer are independently selected from hydrogen, substituted or unsubstituted Cre alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2.6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 71 , R 71' and R 71” are independently selected from hydrogen, substituted or unsubstituted Ci -6 alkyl, substituted or unsubstituted C 2 -e alkenyl, and substituted or unsubstituted C 2-6 alkynyl; preferably R 71 is hydrogen or substituted or unsubstituted C 1-6 alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Rsi , Rer and R 8 r are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R 82 , R S2 · and Re are independently selected from hydrogen, substituted or unsubstituted Ci-e alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R S3 , R S3 · and Rs 3” are independently selected from hydrogen, substituted or unsubstituted C 1-6 alkyl, substituted or unsubstituted C 2-6 alkenyl, and substituted or unsubstituted C 2-6 alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein p is 0, 1 or 2; and/or q is 0 or 1 ; and/or n is 0 or 1 ; and/or m is 0 or 1. and/or r is 0 or 1. and/or t is 0 or 1. and/or

X is selected from a bond or a substituted or unsubstituted group selected from -CH 2 -, -CH 2 CH 2 - , C(O), -CH 2 C(0)-, -CH 2 CH 2 C(0)-, -NHC(0)CH 2 - and NHC(0)CH 2 CH 2 -; and/or

Yi is -CH 2 -; and/or

and/or R z is hydrogen; and/or

Ri is and/or

R 2 is a substituted or unsubstituted group selected from phenyl and thienyl; and/or

R 3 is substituted or unsubstituted C 1-6 alkyl; more preferably R 3 is substituted or unsubstituted methyl or substituted or unsubstituted ethyl; and/or

R 3' is hydrogen or substituted or unsubstituted methyl; and/or

R 4 and R 4' are both hydrogen; and/or

Rs, Rs·, Rs” and Rs - are all hydrogen;

and/or

Re, Re·, R 6” and R 6 are all hydrogen; and/or

R 7 is selected from substituted or unsubstituted phenyl and substituted or unsubstituted pyridinyl and substituted or unsubstituted thienyl; and/or

Re is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl; and/or

Re· is selected from hydrogen and substituted or unsubstituted methyl; and/or R g and Rg· are selected from hydrogen, halogen and -CN; more preferably Rg and Rg· are selected from hydrogen, fluorine and -CN; and/or

R 10 and Rio· are both hydrogen; and/or

Rio " and Rio - form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl; and/or

R 41 is hydrogen; and/or

R 71 is hydrogen or substituted or insubstituted methyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment p is 0, 1 or 2.

In a preferred embodiment q is O or

In a preferred embodiment n is 0 or 1.

In a preferred embodiment m is 0 or 1.

In a preferred embodiment r is 0 or 1.

In a preferred embodiment t is 0 or 1.

In a preferred embodiment m and r are both 0.

In a preferred embodiment m and r are both 1.

In a preferred embodiment

X is selected from a bond or a substituted or unsubstituted group selected from -CH 2 -, -CH2CH2- , C(O), -CH 2 C(0)-, -CH 2 CH 2 C(0)-, -NHC(0)CH 2 - and NHC(0)CH 2 CH2-.

In a preferred embodiment

In a preferred embodiment

Yi is -CH2-.

In a preferred embodiment

In a preferred embodiment

Yi is -CH2-, while In a preferred embodiment

Yi is -CH 2 -, while

In a preferred embodiment Yi and Y 2 are both -CH 2 -.

In a preferred embodiment R z is hydrogen.

In a preferred embodiment

R2 is a substituted or unsubstituted group selected from phenyl and thienyl.

In a preferred embodiment R 3 is substituted or unsubstituted Ci -6 alkyl; more preferably R 3 is substituted or unsubstituted methyl or substituted or unsubstituted ethyl.

In a preferred embodiment

R 3' is hydrogen or substituted or unsubstituted methyl.

In a preferred embodiment R 3 is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl, while R 3 · is selected from substituted or unsubstituted methyl and hydrogen.

In a preferred embodiment

R 3 is substituted or unsubstituted methyl, while R 3 · is selected from substituted or unsubstituted methyl and hydrogen. In a preferred embodiment

R 3 is substituted or unsubstituted ethyl, while R 3 - is hydrogen.

In a preferred embodiment

R 3 and R 3 · are both substituted or unsubstituted methyl.

In a preferred embodiment

R 4 and R 4' are both hydrogen.

In a preferred embodiment Rs, Rs·, Rs- and R5 are all hydrogen.

In a preferred embodiment

Re, Re·, R 6" and Re- are all hydrogen.

In a preferred embodiment R 7 is selected from substituted or unsubstituted phenyl and substituted or unsubstituted pyridinyl and substituted or unsubstituted thienyl.

In a preferred embodiment

Re is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl. In a preferred embodiment

Re· is selected from hydrogen and substituted or unsubstituted methyl.

In a preferred embodiment

Rs is selected from substituted or unsubstituted methyl and substituted or unsubstituted ethyl, while Rs· is selected from hydrogen and substituted or unsubstituted methyl.

In a preferred embodiment

Rs is substituted or unsubstituted methyl, while Rs· is selected from hydrogen and substituted or unsubstituted methyl. In a preferred embodiment

Rs is substituted or unsubstituted ethyl, while Rs· is selected from hydrogen.

In a preferred embodiment

Rs and Rs· are both substituted or unsubstituted methyl. In a preferred embodiment

Rg and Rg· are selected from hydrogen, halogen and -CN; more preferably Rg and Rg· are selected from hydrogen, fluorine and -CN. In a preferred embodiment

Rg is hydrogen.

In a preferred embodiment

Rg· is selected from hydrogen, halogen and -CN; more preferably Rg· is selected from hydrogen, fluorine and -CN. In a preferred embodiment

Rg is hydrogen, while Rg· is selected from hydrogen, fluorine and -CN.

In a preferred embodiment

Rg is hydrogen, while Rg· is fluorine.

In a preferred embodiment Rg is hydrogen, while Rg· is -CN.

In a preferred embodiment

Rg and Rg· are both hydrogen.

In a preferred embodiment

Rio and Rio are both hydrogen. In a preferred embodiment

Rio·· and Rio- are both hydrogen.

In a preferred embodiment Rio · and Rio- form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl.

In a preferred embodiment

Rio and Rio are both hydrogen while R«r and Rio- form, with the carbon atom to which they are attached, a substituted or unsubstituted cyclopropyl.

In a preferred embodiment

R 10 , Rio\ Rio- and Rio- are all hydrogen.

In a preferred embodiment

R 4 I is hydrogen.

In a preferred embodiment

Rn is hydrogen or substituted or insubstituted methyl.

In an embodiment of the compound according to the invention of general Formula (I), the halogen is fluorine, chlorine, iodine or bromine; preferably fluorine, optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In an embodiment of the compound according to the invention of general Formula (I), the haloalkyl is -CF3 ; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another embodiment of the compound according to the invention of general Formula (I), the haloalkoxy is -OCF3; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred further embodiment, the compounds of the general Formula (I) are selected from

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred further embodiment, the compounds of the general Formula (I) are selected from

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as dual ligands of the a2d subunit, particularly the a2d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor it is a very preferred embodiment in which the compounds are selected which act as dual ligands of the a2d subunit, particularly the a2d-1 subunit, of the voltage-gated calcium channel and the m-opioid receptor and especially compounds which have a binding expressed as K, responding to the following scales:

K,(m) is preferably < 1000 nM, more preferably < 500 nM, even more preferably < 100 nM.

Kϊ(a2d1 ) is preferably < 10000 nM, more preferably < 5000 nM, even more preferably < 500 nM.

In the following the phrase“compound of the invention” is used. This is to be understood as any compound according to the invention as described above according to general Formula (I), (P), (l a ), (l a ’), (l b ), (l b ’) > (I 3 ) and (IZ).

The compounds of the invention represented by the above described Formula (I) may include enantiomers depending on the presence of chiral centres or isomers depending on the presence of multiple bonds (e.g. Z, E). The single isomers, enantiomers or diastereoisomers and mixtures thereof fall within the scope of the present invention.

For the sake of clarity the expression“a compound according to Formula (I), wherein e.g. Ri, R 2 , R 3 , R3 , R 4 , R 4' , X, Ui , Y2 and n are as defined below in the detailed description” would (just like the expression“a compound of Formula (I) as defined in any one of claims e.g. 1 to 8” found in the claims) refer to“a compound according to Formula (I)”, wherein the definitions of the respective substituents Ri etc. (also from the cited claims) are applied. In addition, this would also mean, though (especially in regards to the claims) that also one or more disclaimers defined in the description (or used in any of the cited claims like e.g. claim 1 ) would be applicable to define the respective compound. Thus, a disclaimer found in e.g. claim 1 would be also used to define the compound“of Formula (I) as defined in any one of the corresponding related claims e.g. 1 to 8”.

In general the processes are described below in the experimental part. The starting materials are commercially available or can be prepared by conventional methods. A preferred aspect of the invention is also a process for the production of a compound according to Formula (I), following scheme 1 , scheme 2, scheme 3, scheme 4, scheme 5, scheme 6 or scheme 7.

Two different general methods have been developed for obtaining the compounds of the invention, as described below in methods A and B, and further detailed in Schemes 1 to 7.

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein, if not defined otherwise, Ri, R 2 , R 3 , Ry, R 4 , R 4' , X, Y 1 , Y 2 and n have the meanings defined in the description. LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate).

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein X represents a bond, and wherein Ri, R 2 , R3, Rr, R4, R^, Ui, Y2 and n have the meanings as defined in the description, said process comprises treating a compound of formula (lla),

wherein Q represents chloro, bromo, iodo or triflate, with a suitable reagent of formula (M I-1 )

R r H

III-1 under standard Buchwald-Hartwig arylation conditions.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[Chhlp-, and wherein Ri, R 2 , R 3 , R3', R 4 , R 4 , Yi, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (Mb)

wherein r represents 0 to 4, with a reagent of formula (III-1 )

R H

111-1 under standard reductive amination conditions.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[Chfelp-, and wherein Ri, R 2 , R3, R3', R 4 , R 4 , Ui, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (lla),

lla wherein Q represents chloro, bromo, iodo or triflate, with an organometallic reagent of formula (MI-2)

M

j ]

Ri P

MI-2 wherein M represents a suitable organometallic group, preferably a boron or zinc reagent, and p has the meaning as defined in the description.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[CH 2 ] P C(0)[CH 2 ]q- and q is 0, and wherein Ri , R 2l R3, R3', R 4 , R 4 , YI , Y 2 , n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (lie)

with a reagent of formula (111-1 )

R r H

III-1 under conventional amidation conditions.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[CH 2 ] P N(R z )C(0)[CH 2 ] q -, and wherein Ri, R 2 , R3, R3·, R 4 , R 4 ·, Ui, Y 2 , n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (VI)

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, p, q and Rz have the meanings as defined in the description, with a reagent of formula (111-1 )

R H

III-1 under conventional alkylation conditions.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[CH 2 ]pN(R 2 )C(0)[CH2] q -, and wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, Yi, Y2, n, p and q have the meanings as defined in the description, said process comprises treating an amino compound of formula (lid)

wherein p and Rz have the meanings as defined in the description, with an acyl reagent of formula (III-3),

z

in-3 under amidation conditions, wherein Z represents OH or halogen and q has the meaning as defined in the description.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein -X- represents -[CH 2 ]pN(Rz)C(0)[CH 2 ] q -, p is 0, and wherein Ri, R 2 , R3, R 3 , R 4 , R 4' , YI , Y 2 , n, p and q have the meanings as defined in the description, said process comprises reacting a compound of formula (lla)

lla wherein Q represents chloro, bromo, iodo or triflate, with a carboxamido compound of formula (MI-5)

ill-5 under Ullmann or Buchwald-Hartwig arylation conditions, wherein q and Rz have the meanings as defined in the description.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein n is 0, and wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 ·, X, Y 1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alkylating agent of formula (VIII) wherein Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate nosylate or triflate.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein n is 0, and wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 , X, Y 1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alcohol of formula (VIII), wherein Z represents OH, under conventional Mitsunobu conditions.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein n is 0, and wherein Ri, R2, R3, R3', R 4 , R 4 ·, X, Y 1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is halogen,

Vila with an agent of formula (VIII) in the presence of a strong base, wherein Z represents OH.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

wherein n is 1 , and wherein R1, R 2 , R3, R3', R 4 , R 4 ·, X, Y1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (VI lb)

with an agent of formula (VIII), under standard alkylation reaction conditions, wherein either Z represents OH and G represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, or alternatively Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate and G represents OH.

In a particular embodiment there is a process for the production of a compound according to Formula (I),

a) wherein X represents a bond, and wherein Ri, R 2 , R3, R3 , R 4 , R 4 , Y1 , Y2 and n have the meanings as defined in the description, said process comprises treating a compound of formula (I la),

lla wherein Q represents chloro, bromo, iodo or triflate, with a suitable reagent of formula (111-1 )

R r H

MI-1 under standard Buchwald-Hartwig arylation conditions, or b) wherein -X- represents -[CH 2 ] P -, and wherein R1 , R 2 , R3, R3', R 4 , R 4 ·, Ui, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (lib) wherein r represents 0 to 4, with a reagent of formula (III-1)

R r H

111-1 under standard reductive amination conditions, or c) wherein -X- represents -[CH 2 ] P -, and wherein Ri , R 2 , R3, R3', R 4 , R 4' , Yi, Y2 and n and p have the meanings as defined in the description, said process comprises treating a compound of formula (lla),

wherein Q represents chloro, bromo, iodo or triflate, with an organometallic reagent of formula (III-2)

M

Ji j

Ri P

MI-2 wherein M represents a suitable organometallic group, preferably a boron or zinc reagent, and p has the meaning as defined in the description, or d) wherein -X- represents -[CH 2 ] P C(0)[CH 2 ]q- and q is 0, and wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, YI , Y2, n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (lie)

with a reagent of formula (III-1)

R r H

III-1 under conventional amidation conditions, or e) wherein -X- represents -[CH 2 ] p N(R z )C(0)[CH 2 ] q -, and wherein R1, R 2 , R 3 , R3', R 4 , R 4 ·, Yi, Y 2 , n, p and q have the meanings as defined in the description, said process comprises treating a compound of formula (VI)

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, p, q and Rz have the meanings as defined in the description, with a reagent of formula (III-1) R r H

111-1 under conventional alkylation conditions, or f) wherein -X- represents -[CH 2 ]pN(R z )C(0)[CH 2 ] q -, and wherein Ri, R å , R 3 , R 3' , R 4 , R 4 ·, Yi, Y 2 , n, p and q have the meanings as defined in the description, said process comprises treating an amino compound of formula (lid)

wherein p and Rz have the meanings as defined in the description, with an acyl reagent of formula (III-3),

z½, R '

III-3 under amidation conditions, wherein Z represents OH or halogen and q has the meaning as defined in the description, or g) wherein -X- represents -[CH 2 ]pN(R z )C(0)[CH 2 ] q -, p is 0, and wherein Ri, R 2 , R 3 , R 3 , R 4 , R 4 ·, YI , Y 2 , n, p and q have the meanings as defined in the description, said process comprises reacting a compound of formula (lla)

lla wherein Q represents chloro, bromo, iodo or triflate, with a carboxamido compound of formula (111 -5)

under Ullmann or Buchwald-Hartwig arylation conditions, wherein q and R z have the meanings as defined in the description, or h) wherein n is 0, and wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, X, Y1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alkylating agent of formula (VIII) wherein Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, or i) wherein n is 0, and wherein R1, R 2 , R3, R3', R 4 , R 4 ·, X, Y1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is OH,

Vila with an alcohol of formula (VIII), wherein Z represents OH, under conventional Mitsunobu conditions or j) wherein n is 0, and wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, X, Y1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (Vila) wherein G is halogen,

Vila with an agent of formula (VIII) in the presence of a strong base, wherein Z represents OH, or k) wherein n is 1 , and wherein Ri, R 2 , R3, R3', R 4 , R 4 , X, Y1 and Y 2 have the meanings as defined in the description, said process comprises reacting a compound of formula (VI lb)

with an agent of formula (VIII), under standard alkylation reaction conditions, wherein either Z represents OH and G represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, or alternatively Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate and G represents OH.

In a particular embodiment there is a process for the production of a compound according to Formula (I), by the reduction reaction of a carbonyl derivative with a suitable reductive reagent, preferably sodium borohydride, in an organic solvent, preferably MeOH, to afford a hydroxyl compound.

In a particular embodiment there is a process for the production of a compound according to Formula (I), by deprotection reaction of a compound of formula I that contains an amine protecting group such as a carbamate, preferably terf-butoxy carbonyl, by any suitable method, such as treatment with an acid, preferably HCI or trifluoroacetic acid in an appropriate solvent such as 1 ,4-dioxane, DCM, ethyl acetate or a mixture of an organic solvent and water.

In a particular embodiment there is a process for the production of a compound according to Formula (I), by reductive amination reaction of a compound of formula I that contains an amino group with an aldehyde, preferably carried out with a reductive reagent, preferably sodium triacetoxyborohydride, in an organic solvent, preferably DCE, in the presence of an organic base, preferably DIPEA or TEA. Alternatively, the reaction can be carried out in the presence of an acid, preferably acetic acid. In a particular embodiment there is a process for the production of a compound according to Formula (I), by reaction of a compound of formula I that contains an amino group with an alkylating reagent, in the presence of a base, preferably DIPEA or K2CO3, in an organic solvent, preferably acetonitrile, at suitable temperature, such as in the range of 0-120 °C.

In a particular embodiment there is a process for the production of a compound according to Formula (I), by reaction of a compound of formula I that contains an amino group with a vinyl derivative, in an organic solvent, preferably 2-methoxyethanol, at suitable temperature, such as in the range of 20-140 °C.

A particular embodiment of the invention refers to the use of a compound of Formula

(II),

II

wherein Z represents OH or halogen, R 2 , R 3 , R3 , R 4 , R 4 , Ui, Y2 and n have the meanings as defined in the description, for the preparation of compounds of Formula

(I).

A particular embodiment of the invention refers to the use of a compound of Formula (lla),

wherein Q represents chloro, bromo, iodo or triflate, R 2 , R 3 , R3', R 4 , R 4 ·, Ui, Y2 and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (ll-LG),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Z represents OH or halogen, R 2 , R 4 , R 4 , Y1, Y 2 and n have the meanings as defined in the description, for the preparation of compounds of Formula

(I)·

A particular embodiment of the invention refers to the use of a compound of Formula (lla-LG),

lla-LG

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Q represents chloro, bromo, iodo or triflate, R 2 , R 4 , R 4 , Yi, Y 2 and n have the meanings as defined in the description, for the preparation of compounds of Formula (I). A particular embodiment of the invention refers to the use of a compound of Formula (Mb),

wherein R 2 , R 3 , R 3' , R 4 , R 4 ·, Yi, Y 2 , n and r have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (llb-LG),

llb-LG

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R 2 , R 4 , R 4 ·, Yi, Y 2 , n and r have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula

(He),

wherein R 2 , R 3 , R 3 , R 4 , R 4 ·, Yi, Y 2 , n and p have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (llc-LG),

llc-LG

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R 2 , R 4 , R 4 ·, Yi, Y 2 , n and p have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (lid),

wherein R 2 , R 3 , R 3 ·, R 4 , R 4 ·, Yi, Y 2 , n, p and R z have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (lld-LG),

lld-LG

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R 2 , R 4 , R 4 ·, Yi, Y2, n, p and R z have the meanings as defined in the description, for the preparation of compounds of Formula (i).

A particular embodiment of the invention refers to the use of a compound of Formula

(HI-1 ),

wherein R1 has the meaning as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (HI-2),

wherein p and R1 have the meaning as defined in the description, and M represents a suitable organometallic group, preferably a boron or zinc reagent, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (MI-3),

wherein q and Ri have the meaning as defined in the description, and Z represents OH or halogen, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (MI-4),

III-4

wherein q has the meaning as defined in the description, Z represents OH or halogen, and LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (MI-5),

wherein q, R z and Ri have the meaning as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IV),

IV wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Ri, R 2 , R 4 , R 4 ·, X, Yi, Y 2 and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IVa),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Ri, R 2 , R 4 , R 4 ·, Ui, Y2 and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IVb),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R1, R 2 , R 4 , R 4 ·, Yi, Y 2, p and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IVc),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Ri , R 2 , R 4 , R 4 ·, Yi , Y 2, p and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IVd),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R z, Ri , R 2 , R 4 , R 4 ·, Yi , Y 2, p and n have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IVe),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, Ri , R 2 , R 4 , R 4 ·, Yi and Y 2 have the meanings as defined in the description, for the preparation of compounds of Formula (I). A particular embodiment of the invention refers to the use of a compound of Formula (IVf),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R 1 , R 2 , R 4 , R 4 ·, Y 1 and Y 2 have the meanings as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (V),

HNR3R3'

v

wherein R 3 and R 3 have the meaning as defined in the description, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (VI),

wherein R 2 , R 3 , R 3 , R 4 , R 4 ·, Yi, Y 2 , n, p, q and R z have the meanings as defined in the description, and LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, for the preparation of compounds of Formula (I). A particular embodiment of the invention refers to the use of a compound of Formula (VII),

Vii

wherein n, Ri, R 4 , R 4 · and X have the meanings as defined in the description, and G is OH or halogen, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (Vila),

Vila

wherein Ri, R 4 , R 4 · and X have the meanings as defined in the description, and G is OH or halogen, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (VI lb),

wherein Ri, R , R 4 · and X have the meanings as defined in the description, and G is OH or a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, for the preparation of compounds of Formula (I). A particular embodiment of the invention refers to the use of a compound of Formula (VIII),

wherein R 2 , R3, R3', YI, and Y 2 have the meaning as defined in the description, and Z represents OH or halogen, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (VIII-LG),

wherein LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, R 2 , Yi, and Y 2 have the meaning as defined in the description, and Z represents OH or halogen, for the preparation of compounds of Formula (I).

A particular embodiment of the invention refers to the use of a compound of Formula (IX),

IX

wherein n, R 4 , R 4 · have the meanings as defined in the description, and Z represents OH or halogen and G is OH or halogen, for the preparation of compounds of Formula

(I)·

A particular embodiment of the invention refers to the use of a compound of Formula II, ll-LG, lla, lla-LG, Mb, llb-LG, lie, llc-LG, lid, lld-LG, III-1 , MI-2, IM-3, MI-4, IM-5, IV, IVa, IVb, IVc, IVd, IVe, IVf, V, VI, VII, Vila, Vllb, VIII, VIII-LG or IX,

wherein R 1 , R 2 , R 3 , R 3' , R 4 , R 4 ·, X, Y 1 , Y 2 , n, p, q, r and R z have the meanings as defined in the description, Q represents chloro, bromo, iodo or triflate, LG represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, have the meanings as defined in the description, M represents a suitable organometallic group, Z represents OH or halogen, and G is OH, halogen or a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, for the preparation of compounds of Formula (I). The obtained reaction products may, if desired, be purified by conventional methods, such as crystallisation and chromatography. Where the above described processes for the preparation of compounds of the invention give rise to mixtures of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. If there are chiral centers the compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution.

One preferred pharmaceutically acceptable form of a compound of the invention is the crystalline form, including such form in pharmaceutical composition. In the case of salts and also solvates of the compounds of the invention the additional ionic and solvent moieties must also be non-toxic. The compounds of the invention may present different polymorphic forms, it is intended that the invention encompasses all such forms.

Another aspect of the invention refers to a pharmaceutical composition which comprises a compound according to the invention as described above according to general formula I or a pharmaceutically acceptable salt or steroisomer thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle. The present invention thus provides pharmaceutical compositions comprising a compound of this invention, or a pharmaceutically acceptable salt or stereoisomers thereof together with a pharmaceutically acceptable carrier, adjuvant, or vehicle, for administration to a patient.

Examples of pharmaceutical compositions include any solid (tablets, pills, capsules, granules etc.) or liquid (solutions, suspensions or emulsions) composition for oral, topical or parenteral administration.

In a preferred embodiment the pharmaceutical compositions are in oral form, either solid or liquid. Suitable dose forms for oral administration may be tablets, capsules, syrops or solutions and may contain conventional excipients known in the art such as binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers, for example lactose, sugar, maize starch, calcium phosphate, sorbitol or glycine; tabletting lubricants, for example magnesium stearate; disintegrants, for example starch, polyvinylpyrrolidone, sodium starch glycollate or microcrystalline cellulose; or pharmaceutically acceptable wetting agents such as sodium lauryl sulfate. The solid oral compositions may be prepared by conventional methods of blending, filling or tabletting. Repeated blending operations may be used to distribute the active agent throughout those compositions employing large quantities of fillers. Such operations are conventional in the art. The tablets may for example be prepared by wet or dry granulation and optionally coated according to methods well known in normal pharmaceutical practice, in particular with an enteric coating.

The pharmaceutical compositions may also be adapted for parenteral administration, such as sterile solutions, suspensions or lyophilized products in the apropriate unit dosage form. Adequate excipients can be used, such as bulking agents, buffering agents or surfactants.

The mentioned formulations will be prepared using standard methods such as those described or referred to in the Spanish and US Pharmacopoeias and similar reference texts.

Administration of the compounds or compositions of the present invention may be by any suitable method, such as intravenous infusion, oral preparations, and intraperitoneal and intravenous administration. Oral administration is preferred because of the convenience for the patient and the chronic character of the diseases to be treated.

Generally an effective administered amount of a compound of the invention will depend on the relative efficacy of the compound chosen, the severity of the disorder being treated and the weight of the sufferer. However, active compounds will typically be administered once or more times a day for example 1 , 2, 3 or 4 times daily, with typical total daily doses in the range of from 0.1 to 1000 mg/kg/day.

The compounds and compositions of this invention may be used with other drugs to provide a combination therapy. The other drugs may form part of the same composition, or be provided as a separate composition for administration at the same time or at different time.

Another aspect of the invention refers to the use of a compound of the invention or a pharmaceutically acceptable salt or isomer thereof in the manufacture of a medicament. Another aspect of the invention refers to a compound of the invention according as described above according to general formula I, or a pharmaceutically acceptable salt or isomer thereof, for use as a medicament for the treatment of pain. Preferably the pain is medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia. This may include mechanical allodynia or thermal hyperalgesia.

Another aspect of the invention refers to the use of a compound of the invention in the manufacture of a medicament for the treatment or prophylaxis of pain.

In a preferred embodiment the pain is selected from medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia, also preferably including mechanical allodynia or thermal hyperalgesia.

Another aspect of this invention relates to a method of treating or preventing pain which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound as above defined or a pharmaceutical composition thereof. Among the pain syndromes that can be treated are medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia, whereas this could also include mechanical allodynia or thermal hyperalgesia.

The present invention is illustrated below with the aid of examples. These illustrations are given solely by way of example and do not limit the general spirit of the present invention.

General Experimental Part (Methods and Equipment of the synthesis and analysis

SYNTHESIS DESCRIPTION Two different general methods have been developed for obtaining the compounds of the invention, as described below in methods A and B, and further detailed in Schemes 1 to 7.

METHOD A A one-step process is described for the preparation of compounds of general formula (I) starting from a compound of formula (II), as shown in the following scheme:

II A=NR 3 R 3 · , I A=NR 3 R 3 .

HNR3R3. V

ll-LG A=LG V IV A=LG -^ V

Method A

wherein Ri, R 2 , R 3 , R 3' , R 4 , R^, X, Yi, Y2 and n have the meanings as defined in claim 1 , LG represents a leaving group, and Z represents a suitable functional group to perform such transformation, and RrW represents a compound of formula 111-1 , III-2, III-3 or MI-5, as it is detailed below in Schemes 1 to 4.

In addition, the amino group NR 3 R 3' present in a compound of formula (I) can be incorporated later in the synthesis by reaction of a compound of formula (IV) wherein LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate) with an amine of formula (V) to render a compound of formula (I) as shown in the scheme above. The alkylation reaction is carried out in a suitable solvent, such as ethanol, dimethylformamide, dimethylsulfoxide or acetonitrile, preferably ethanol; using an excess of amine (V) or optionally in the presence of a base such as K 2 CO 3 , A/./V-diisopropylethylamine or triethylamine; at a suitable temperature comprised between room temperature and the reflux temperature, preferably heating, or alternatively, the reactions can be carried out under microwave heating. Additionally, an activating agent such as sodium iodide or potassium iodide can be used. Such transformation can also be performed starting from a compound of formula (ll-LG) to prepare a compound of formula (II).

Scheme 1

The general synthetic route according to method A for preparing compounds of formula (I) wherein X represents a bond, resulting in compounds of formula (la) starting from a compound of formula (lla) is represented in Scheme 1 :

HNR3R3.

V wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 ·, Ui, Y2 and n have the meanings as defined in claim 1 , Q represents chloro, bromo, iodo or triflate and LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate).

The preparation of a compound of formula (la) from a compound of formula (lla) is carried out by treating a compound of formula (lla) with a suitable reagent of formula (MI-1 ) under standard Buchwald-Hartwig arylation conditions, using a Pd catalyst such as tris(dibenzylideneacetone)dipalladium(0) or palladium acetate, and a suitable ligand, preferably a phosphine ligand such as BINAP or XPhos, using a suitable base such as sodium tert- butoxide or cesium carbonate, in a suitable solvent such as toluene or 1 ,4-dioxane, at a suitable temperature, preferably heating. Alternatively, the reaction can be carried out under Ullmann arylation conditions, using a Cu catalyst such as copper iodide and a suitable ligand, preferably an amino ligand such as L/ 1 ,L/ 2 - dimethylethane-1 ,2-diamine, in the presence of a suitable base such as potassium phosphate or potassium carbonate, in a suitable solvent such as 1 ,4-dioxane or dimethylformamide, at a suitable temperature, preferably heating.

Alternatively, the amino group NR 3 R 3 · present in a compound of formula (la) or (lla) can be incorporated later in the synthesis by reaction of a precursor compound of formula (IVa) or (lla-LG), respectively, with an amine of formula (V) following the conditions described above in Method A.

Scheme 2 The general synthetic route according to method A for preparing compounds of formula (I) wherein -X- represents -[CH 2 ] P -, resulting in compounds of formula (lb), starting from a compound of formula (lla) or (Mb), is represented in Scheme 2:

wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 ·, Yi, Y 2 , n and p have the meanings as defined in claim 1 , LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate), Q represents chloro, bromo, iodo or triflate, M represents a suitable organometallic group (preferably a boron or zinc reagent) and r represents 0 to 4.

The preparation of a compound of formula (lb) from an aldehyde compound of formula (lib) can be carried out by treating a compound of formula (lib) with a reagent of formula (111-1 ) under standard reductive amination conditions. The reaction is carried out in the presence of a reductive reagent, such as sodium triacetoxyborohydride, sodium borohydride or sodium cyanoborohydride, in a suitable solvent, preferably tetrahydrofuran, dichloroethane or methanol, optionally in the presence of an acid (preferably acetic acid) or a base (preferably A/,A/-diisopropylethylamine).

Alternatively, a compound of formula (lb) can be prepared by reacting a compound of formula (!!a) with an organometallic reagent of formula (III-2), preferably a boron or zinc reagent. The coupling reaction is carried out under conventional coupling procedures described in the literature, using a suitable catalyst (preferably a Pd catalyst) and a suitable ligand (preferably a phosphine ligand), such as for example tetrakis(triphenylphosphine)palladium(0), or palladium acetate and XPhos, in the presence of a suitable base such as potassium carbonate or cesium carbonate, in a suitable solvent such as tetrahydrofuran, 1 ,2-dimethoxyethane or 1 ,4-dioxane, or mixtures thereof with water. In addition, the amino group NR3R3' present in a compound of formula (lb), (lla) or (lib) can be incorporated later in the synthesis by reaction of a precursor compound of formula (IVb), (lla-LG) or (llb-LG), respectively, with an amine of formula (V), following the conditions described above in Method A.

Scheme 3

The general synthetic route according to method A for preparing compounds of formula (I) wherein -X- represents -[CH 2 ] P C(0)[CH 2 ] q - and q is 0, resulting in compounds of formula (lc), starting from a compound of formula (lie) is represented in Scheme 3:

wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 , Yi, Y 2 , n and p have the meanings as defined in claim 1 and LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate).

The preparation of a compound of formula (lc) from an acid compound of formula (lie) and a reagent of formula (MI-1) can be carried out under conventional amidation conditions. As a way of example, the reaction is carried out using a suitable coupling reagent such as A/-(3-dimethylaminopropyl)-A/'-ethylcarbodiimide (EDC), dicyclohexylcarbodiimide (DCC), A/-[(dimethylamino)-1 H-1 ,2,3-triazolo-[4,5-/)]pyridin- 1-ylmethylene]-A/-methylmethanaminium hexafluorophosphate N- oxide (HATU) or A/,/\/,A/',/\/'-tetramethyl-0-(1/-/-benzotriazol-1-yl)uroniu m hexafluorophosphate (HBTU), optionally in the presence of 1-hydroxybenzotriazole, optionally in the presence of an organic base such as /V-methylmorpholine or A/,/V-diisopropylethylamine, in a suitable solvent such as dichloromethane or dimethylformamide, and at a suitable temperature, preferably at room temperature. Alternatively, the amidation can be performed in two steps by first converting an acid of formula (lie) into its corresponding acyl halide following standard conditions described in the literature, and then reacting it with a compound of formula (111-1 ) in a suitable solvent, such as dichloromethane, tetrahydrofuran, ethyl acetate or ethyl acetate-water mixtures; in the presence of an organic base such as triethylamine or A/./V-diisopropylethylamine or an inorganic base such as K 2 CO 3 ; and at a suitable temperature, preferably comprised between 0 °C and room temperature. Additionally, an activating agent such as 4-dimethylaminopyridine can be used.

In addition, the amino group NR 3 R 3' present in a compound of formula (lc) or (lie) can be incorporated later in the synthesis by reaction of a precursor compound of formula (IVc) or (llc-LG), respectively, with an amine of formula (V) following the conditions described above in Method A.

Scheme 4

The general synthetic route according to method A for preparing compounds of formula (I) wherein -X- represents -[CH2] P N(R z )C(0)[CH 2 ]q-, resulting in compounds of formula (Id), starting from a compound of formula (lid) or (lla), is represented in Scheme 4: wherein Ri, R 2 , R 3 , R 3' , R 4 , R-r, Rz, Yi, Y2, n, p and q have the meanings as defined in claim 1 , LG represents a leaving group (such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate) and Z represents OH or halogen (preferably bromo or chloro).

The reaction between an amino compound of formula (lid) with an acyl reagent of formula (III-3) to render a compound of formula (Id) can be carried out under the amidation conditions described above in Scheme 3 for the preparation of compounds of formula (lc). Alternatively, the compounds of formula (Id) can be prepared in 2 steps by treating a compound of formula (lid) with an acylating agent of formula (III-4) under the same amidation conditions to obtain a compound of formula (VI), followed by reaction with a reagent of formula (III-1 ), under conventional alkylation conditions such as those described in Method A for the reaction of a compound of formula (IV) with an amine of formula (V). Finally, a compound of formula (Id) wherein p is 0 can be alternatively prepared by reacting a compound of formula (lla) with a carboxamido compound of formula (MI-5). The reaction can be carried out under Ullmann arylation conditions, using a Cu catalyst such as copper iodide and a suitable ligand, preferably an amino ligand such as L/ 1 ,/V 2 - dimethylethane-1 ,2-diamine, in the presence of a suitable base such as potassium phosphate, in a suitable solvent such as 1 ,4-dioxane or dimethylformamide, at a suitable temperature, preferably heating. Alternatively, the coupling reaction can be performed under standard Buchwald-Hartwig arylation conditions, using a suitable Pd catalyst and a suitable ligand (preferably a phosphine ligand).

In addition, the amino group NR3R3' present in a compound of formula (Id), (lla) or (lid) can be incorporated later in the synthesis by reaction of a precursor compound of formula (IVd), (lla-LG) or (lld-LG), respectively, with an amine of formula (V) following the conditions described above in Method A.

METHOD B

An alternative one-step process is described for the preparation of compounds of general formula (I) starting from a compound of formula (VII), as shown in the following scheme:

Method B

wherein Ri, R 2 , R3, R 3' , R 4 , R 4 ·, X, Ui, Y2 and n have the meanings as defined in claim 1 , Z represents OH or a leaving group, and G represents OH, halogen or a leaving group depending on the meaning of n. Specific reaction conditions are detailed below in Schemes 5 and 6.

As it has been mentioned before, alternatively the amino group NR3R3' present in a compound of formula (I) can be incorporated later in the synthesis by reaction of a precursor compound of formula (IV) with an amine of formula (V) following the conditions described above in Method A. Scheme 5

The general synthetic route according to method B for preparing compounds of formula (I) wherein n is 0, resulting in compounds of formula (le), is represented in Scheme 5:

IVe A=LG 3 V HNR3R3' wherein Ri, R 2 , R 3 , R 3' , R 4 , R 4 ·, X, Y 1 and Y 2 have the meanings as defined in claim 1 , n is 0, Z represents OH or a leaving group, and G represents OH or halogen.

Depending on the meaning of G and Z different reaction conditions will apply: a) When G is OH and Z represents a leaving group such as chloro, bromo, iodo, mesylate, tosylate, nosylate or triflate, the alkylation reaction between a phenol of formula (Vila) and an alkylating agent of formula (VIII) is carried out in a suitable solvent, such as dimethylformamide, dimethylacetamide, dimethylsulfoxide, acetonitrile, dichloromethane or 1 ,4-dioxane; in the presence of a base such as K 2 C0 3 , Cs 2 C0 3 , sodium hydride or potassium tert- butoxide; at a suitable temperature comprised between room temperature and the reflux temperature, or alternatively, the reactions can be carried out in a microwave reactor. Additionally, an activating agent such as sodium iodide can be used. b) When G is OH and Z represents OH, the reaction is carried out under conventional Mitsunobu conditions by treating a phenol of formula (Vila) with an alcohol of formula (VIII) in the presence of an azo compound such as 1 ,1 '- (azodicarbonyl)dipiperidine (ADDP), diisopropylazodicarboxylate (DIAD) or diethyl azodicarboxylate (DEAD) and a phosphine such as tributylphosphine or triphenylphoshine. The Mitsunobu reaction is carried out in a suitable solvent, such as toluene or tetrahydrofuran; at a suitable temperature comprised between room temperature and the reflux temperature. c) When G is halogen and Z represents OH, the reaction is carried out under conventional aromatic nucleophilic substitution conditions by treating an alcohol of formula (VIII) with a compound of formula (Vila) wherein G represents halogen (preferably fluoro), in the presence of a strong base such as sodium hydride or potassium terf-butoxide. The reaction is carried out in a suitable solvent, such as a polar aprotic solvent, preferably dimethylformamide, dimethylacetamide or dimethylsulfoxide; at a suitable temperature comprised between room temperature and the reflux temperature, preferably heating, or alternatively, the reactions can be carried out in a microwave reactor. Alternatively, when G is bromo or iodo, the compound of formula (VIII) can be introduced under cross-coupling conditions, using a Pd or Cu catalyst and a suitable ligand.

Scheme 6

The general synthetic route according to method B for preparing compounds of formula (I) wherein n is 1 , resulting in compounds of formula (If), is represented in Scheme 6:

wherein Ri, R 2 , R 3 , R 3 , R 4 , R 4 ·, X, Y 1 and Y 2 have the meanings as defined in claim 1 , n is 1 , and either Z represents OH and G represents a leaving group or alternatively Z represents a leaving group and G represents OH.

The reaction is carried out under standard alkylation reaction conditions such as those described in Scheme 5 above. Scheme 7

The preparation of key compounds of formula (II) and (VII) from a common precursor of formula (IX) is summarized in Scheme 7 below:

VII wherein Ri, R 2 , R3, R3', R 4 , R 4 ·, X, Ui, Y2 and n have the meanings as defined in claim 1 , G and Z have the meanings as defined above in Schemes 1 to 6, and R1-W represents a compound of formula III-1 , III-2, III-3 or MI-5 as defined above in Schemes 1 to 6. The preparation of a compound of formula (VII) from a compound of formula (IX) and a compound of formula (III) can be carried out under the reaction conditions described above in general Method A and further detailed in Schemes 1 to 4.

The preparation of a compound of formula (II) or (ll-LG) from a compound of formula (IX) and a compound of formula (VIII) can be carried out under the reaction conditions described above in general Method B and further detailed in Schemes 5 and 6. The compounds of formula (III), (111-1 ), (III-2), (III-3), (III-4), (MI-5), (V), (VIII) and (IX) used in the methods and schemes disclosed above are commercially available or can be synthesized following common procedures described in the literature.

Moreover, certain compounds of the present invention can also be obtained starting from other compounds of formula (I) by appropriate conversion reactions of functional groups, in one or several steps, using well-known reactions in organic chemistry under standard experimental conditions.

In some of the processes described above it may be necessary to protect the reactive or labile groups present with suitable protecting groups, such as for example Boc ( tert - butoxycarbonyl), Teoc (2-(trimethylsilyl)ethoxycarbonyl) or benzyl for the protection of amino groups, and common silyl protecting groups for the protection of the hydroxyl group. The procedures for the introduction and removal of these protecting groups are well known in the art and can be found thoroughly described in the literature.

In addition, a compound of formula (I) can be obtained in enantiopure form by resolution of a racemic compound of formula (I) either by chiral preparative HPLC or by crystallization of a diastereomeric salt or co-crystal. Alternatively, the resolution step can be carried out at a previous stage, using any suitable intermediate.

Examples

The following abbreviations are used in the examples:

ACN: acetonitrile

ADDP: 1 , 1 '-(azodicarbonyl)dipiperidine

aq.: aqueous

BINAP: 2,2 ! -bis(diphenylphosphino)-1 , 1 '-binaphthyl

Boc: terf-butoxycarbonyl

BuLi: butyllithium

BuOH: butanol

CH: cyclohexane

cone. : concentrated

DCE: dichloroethane

DCM: dichloromethane

Deprot.: deprotection

DIAD: diisopropyl azodicarboxylate

DIBAL-H: diisobutylaluminum hydride

DIPEA: A/,A/-diisopropylethylamine

DMA: A/,A/-dimethylacetamide

DMF: A/,A/-dimethylformamide

DMSO: dimethylsulfoxide

EtOAc: ethyl acetate

EtOH: ethanol

EX: example

h: hour/s

HATU: 0-(7-azabenzotriazol-1 -yl)-A/,A/,A/',/\/ -tetramethyluronium hexafluorophosphate HPLC: high performance liquid chromatography I NT: intermediate

MeOH: methanol

MS: mass spectrometry

Min: minutes

Pd(OAc)2: palladium(ll) acetate

Pd 2 (dba)3: tris(dibenzylideneacetone)dipalladium(0)

Quant: quantitative

Ret.: retention

r.t.: room temperature

Sat: saturated

Sol.: solution

Teoc: 2-(trimethylsilyl)ethoxycarbonyl

TEA: triethylamine

TFA: trifluoroacetic acid

THF: tetrahydrofuran

TMSI: trimethylsilyl iodide (or also named iodotrimethylsilane)

Wt: weight

XPhos: 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl

The following methods were used to determine the HPLC-MS spectra:

Method A

Column: Kinetex EVO 50 x 4.6 mm, 2.6 urn

Temperature: 40 °C

Flow: 2.0 mL/min

Gradient: NH 4 HCO 3 pH 8 : ACN (95:5)— 0.5min— (95:5)— 6.5min— (0:100)— 1 min— (0:100) Sample dissolved approx. 1 mg/mL in NH 4 HCO 3 PH 8/ ACN

Method B

Column: Kinetex EVO 50 x 4.6 mm, 2.6 urn

Temperature: 40 °C

Flow: 1.5 mL/min

Gradient: NH 4 HCO 3 pH 8 : ACN (95:5)— 0.5min— (95:5)— 6.5min— (0: 100)— 2min— (0:100)

Sample dissolved approx. 1 mg/mL in NH 4 HCO 3 PH 8/ ACN Method C

Column: Luna C18 250 x 4,6 mm, 5um

Temperature: 40 °C

Flow: 1 mL/min

Gradient: H 2 O-0.1 %HCOOH /ACN (100:0)— 30min— (0:100)— 10min— (0:100) Sample dissolved approx. 1 mg/mL in ACN

Method D

Column: Gemini C18 30 x 4,6 mm, 3um

Temperature: 40 °C

Flow: 1.5 mL/min

Gradient H 2 O-0.1 %HCOOH / ACN (95:5)— 0.5min— (95:5)— 8.5min - (0:100)—

1 min— (0:100)

Sample dissolved approx. 1 mg/mL in ACN

Method E

Column: Column Eclipse XDB-C18 4.6x150 mm, 5um

Temperature: 40 °C

Flow: 1 mL/min

Gradient H 2 0-0.05% TFA / ACN (95:5)— 7min— (5:95)— 5 min— (5:95)

Sample dissolved approx. 1 mg/mL in ACN

Synthesis of Intermediates Intermediate 1 : (R)-2-(T rimethylsilyl)ethyl (3-(2-bromophenoxy)-3-(thiophen-2- yl)propyl)(ethyl)carbamate

Step 1. (R)-3-(Ethylamino)-1 -(thiophen-2-yl)propan-1 -ol: A solution of ( )-3-chloro-1- (thiophen-2-yl)propan-1-ol (7 g, 39.6 mmol) and ethylamine (70 wt% in water, 31 mL, 396 mmol) in EtOH (175 mL) was heated in a sealed flask at 90 °C overnight. The solvent was evaporated, the residue was dissolved in DCM and it was washed with 1 N NaOH, dried over MgS0 4 , filtered and concentrated to dryness. The crude product (7.74 g) was slurried in methylcyclohexane (5.8 vol, 44 mL) and heated at 60 °C for 1 h. Then, it was allowed to cool down and it was stirred at r.t. for 1 h. The solids were filtered, washed with methylcyclohexane and dried under vacuum to provide the title compound (2.68 g, 36% yield).

Step 2. (f?)-3-(2-Bromophenoxy)-A/-ethyl-3-(thiophen-2-yl)propan-1 -amine: To a solution of the product obtained in Step 1 (0.98 g, 5.3 mmol) and 1 -bromo-2- fluorobenzene (2.29 mL, 21.1 mmol) in DMSO (1.6 mL) under a N 2 atmosphere, potassium tert- butoxide (0.6 g, 5.3 mmol) was added and the reaction mixture was heated at 60 °C for 8 h. It was then cooled to r.t., water was added and the aqueous phase was extracted twice with EtOAc. The combined organic phases were dried over MgS0 4 , filtered and evaporated to dryness. The crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4), to give the title compound (1.14 g, 63% yield).

Step 3. Title compound: To a solution of the product obtained in Step 2 (1.14 g, 3.3 mmol) in DCM (1.5 mL), under a N 2 atmosphere, DIPEA (0.58 mL, 3.3 mmol) and a solution of 4-nitrophenyl (2-(trimethylsilyl)ethyl) carbonate (0.95 g, 3.3 mmol) in DCM (1.5 mL) were added and the mixture was stirred at r.t. overnight. NaHCOs sat. solution was added and it was extracted twice with DCM. The combined organic phases were washed with 2 N NaOH solution, dried over MgS0 4 , filtered and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (1 .46 g, 90% yield).

This method was used for the preparation of Intermediates 2-5 using suitable starting materials:

Intermediate 6: 2-(Trimethylsilyl)ethyl (3-(2-bromophenoxy)-3-(3-fluorothiophen-2- yl)propyl)(methyl)carbamate

Step 1 . 1 -(3-Fluorothiophen-2-yl)-3-(methylamino)propan-1 -one hydrochloride: In a sealed tube, 1-(3-fluorothiophen-2-yl)ethanone (1.1 g, 7.6 mmol), methylamine hydrochloride (0.567 g, 8.39 mmol), paraformaldehyde (0.321 g, 10.6 mmol) and cone. HCI (0.04 ml_, 7.63 mmol) were dissolved in EtOH (3.8 ml.) and the mixture was heated at 1 10 °C overnight. The solvent was evaporated, EtOAc was added and the suspension was stirred at r.t. for 3 h. The solids were filtered, washed with EtOAc and dried under vacuum. The crude product was slurried in a mixture of EtOAc (5.6 ml_) and EtOH (1 .8 ml_) and it was heated to reflux for 1 h. After allowing to cool down, the solids were filtered, washed with EtOAc and dried under vacuum, to afford the title compound (820 mg, 48% yield).

Step 2. 1 -(3-Fluorothiophen-2-yl)-3-(methylamino)propan-1 -ol: To a cooled solution of the product obtained in Step 1 (0.82 g, 3.67 mmol) in MeOH (50 ml_), NaBH 4 (0.416 g, 1 1 mmol) was added portionwise and the mixture was stirred at 0-5 °C for 1 h. NH 4 CI sat. solution was then added (25 mL) and MeOH was distilled off. The aqueous phase was extracted with DCM, dried over MgS0 and concentrated to dryness to afford the title compound (460 mg, 66% yield).

Step 3. 3-(2-Bromophenoxy)-3-(3-fluorothiophen-2-yl)-A/-methylpropan -1 -amine: To a solution of the product obtained in Step 2 (0.81 g, 4.29 mmol) in DMA (8 mL), cooled at 0 °C under a N 2 atmosphere, NaH (60 wt% dispersion in mineral oil, 0.43 g, 1 1 mmol) was added in portions. The suspension was stirred at 0 °C for 30 min and then a solution of 1 -bromo-2-fluorobenzene (0.56 mL, 5.16 mmol) in DMA (3.2 mL) was added. The mixture was heated at 90 °C for 2 h and then it was cooled to 0 °C. Water was slowly added and pH was adjusted to 10 with 1 N NaOH solution. The aqueous phase was extracted with DCM, dried over MgS0 4 and concentrated to dryness to afford the title compound (1.2 g, 81 % yield).

Step 4. Title compound: Following the experimental procedure described in Step 3 of Intermediate 1 , starting from the product obtained in Step 3, the title compound was obtained (496 mg, 29 % yield).

This method was used for the preparation of Intermediate 7 using suitable starting materials:

Intermediate 8: 2-(3-Chloro-1-(thiophen-2-yl)propoxy)benzaldehyde

Step 1. 2-(3-Chloro-1-(thiophen-2-yl)propoxy)benzonitrile: To a solution of 3-chloro-1- (thiophen-2-yl)propan-1-ol (10 g, 52 mmol), triphenylphosphine (15 g, 57.2 mmol) and 2-hydroxybenzonitrile (6.8 g, 57.2 mmol) in dry THF (252 ml_), cooled at 0 °C, DIAD (1 1.5 mL, 58.3 mmol) was added dropwise and the mixture was stirred at r.t. overnight. The solvent was concentrated under vacuum and the residue was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (13.9 g, 96% yield).

Step 2. Title compound: To a solution of the product obtained in Step 1 (4 g, 14.4 mol) in toluene (40 mL), cooled at 0 °C, DIBAL-H (25 wt% solution in toluene, 13.5 mL, 20.2 mmol) was added dropwise and the reaction mixture was stirred at 0-5 °C for 4 h. Then, 10% aq. HCI solution was slowly added to quench the reaction and the mixture was stirred at r.t. for 10 min. It was extracted with EtOAc and the combined organic phases were washed with water and brine, dried over Na2S0 4 and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (4 g, 38% yield).

This method was used for the preparation of Intermediate 9 using suitable starting materials:

(1) 1 M DIBAL-H in DCM was used in Step 2

Intermediate 10: Lithium 2-(3-chloro-1-(thiophen-2-yl)propoxy)benzoate

Step 1. Methyl 2-(3-chloro-1 -(thiophen-2-yl)propoxy)benzoate: To a solution of 3- chloro-1 -(thiophen-2-yl)propan-1 -ol (2 g, 1 1.3 mmol), tributylphosphine (3.4 mL, 13.6 mmol) and methyl 2-hydroxybenzoate (1.45 mL, 11.3 mmol) in dry THF (20 mL), ADDP (3.4 g, 13.6 mmol) was added and the mixture was stirred at r.t. overnight. The reaction crude was filtered through a pad of Celite, washed with THF, and the filtrate was concentrated under vacuum. The crude product was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (1.27 g, 36% yield).

Step 2. Title compound: A solution of the compound obtained in Step 1 (1.05 g, 3.4 mmol) in a mixture of THF (17 mL) and 1 N LiOH solution (17 mL, 17 mmol) was heated at 50 °C overnight. The solvent was evaporated, toluene was added and it was again concentrated to dryness to remove residual water, rendering the title compound (1.76 g, overweight, quantitative yield) as a crude product that was used in the next step without further purification.

This method was used for the preparation of Intermediates 1 1 -12 using suitable starting materials:

Intermediate 13: terf-Butyl (3-(2-bromophenoxy)-3-(thiophen-2- yl)propyl)(methyl)carbamate

Step 1. 2-(1-(2-Bromophenoxy)-3-chloropropyl)thiophene: To a solution of 3-chloro-1- (thiophen-2-yl)propan-1 -ol (2 g, 11.3 mmol), triphenylphosphine (3.5 g, 13.6 mmol) and 2-bromophenol (1.96 g, 1 1.3 mmol) in dry THF (40 mL), cooled at 0 °C under a N 2 atmosphere, DIAD (2.64 mL, 13.6 mmol) was added dropwise and the mixture was stirred at r.t. overnight. The solvent was concentrated to dryness and the residue was slurried in hexane. The suspension was filtered, and the collected solids were washed with hexane and discarded, and the filtrate was concentrated under vacuum to afford the title compound that was used without further purification (3.85 g, quant yield).

Step 2. 3-(2-Bromophenoxy)-/V-methyl-3-(thiophen-2-yl)propan-1 -amine: In a sealed tube, a mixture of the product obtained in Step 1 (3.75 g, 11.3 mmol) and methylamine (33 wt% in EtOH, 30 mL, 226 mmol) was heated at 100 °C overnight. Then, it was concentrated to dryness and the crude product was used in the next step without further purification (3.72 g, quant yield).

Step 3. Title compound: To a solution of the product obtained in Step 2 (3.7 g, 1 1.3 mmol) in terf-butanol (10 mL), 2 N NaOH solution (10 mL) and di-terf-butyl dicarbonate (2.5 g, 11.3 mmol) were added and the reaction mixture was stirred at r.t. overnight. Brine and DCM were added, the phases were separated and the aqueous layer was extracted with DCM. The combined organic phases were washed with brine, dried over MgS0 4 , filtered and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (1.34 g, 28% yield for the 3 steps).

Intermediate 14: terf-Butyl (3-(2-bromophenoxy)-3-phenylpropyl)(methyl)carbamate:

In a sealed tube, a mixture of fe/T-butyl (3-chloro-3-phenylpropyl)(methyl)carbamate (4 g, 14.1 mmol), K 2 CO 3 (5.84 g, 42.3 mmol), Kl (234 mg, 1.41 mmol) and 2-bromophenol (2.4 g, 14.1 mmol) in ACN (92 ml_) was heated at 60 °C overnight. After cooling down to r.t., water was added to the reaction mixture and it was extracted with EtOAc. The combined organic phases were dried over MgS0 4 , filtered and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (2.36 g, 40% yield).

This method was used for the preparation of Intermediate 15 using suitable starting materials:

Intermediate 16: 2-(3-((terf-Butoxycarbonyl)(methyl)amino)-1 -phenylpropoxy)benzoic acid

Step 1. Methyl 2-(3-((terf-butoxycarbonyl)(methyl)amino)-1-phenylpropoxy)be nzoate: Following the experimental procedure described in Intermediate 14, but using methyl 2-hydroxy benzoate instead of 2-bromophenol as starting material, the title compound was obtained (1.48 g, 63% yield).

Step 2. Title compound: To a solution of the compound obtained in Step 1 (1.48 g, 3.7 mmol) in a mixture of THF (7.5 ml_) and water (7.5 ml_), lithium hydroxide monohydrate (1.2 g, 30 mmol) was added and the reaction mixture was heated at 50 °C overnight. The solvent was concentrated, pH was adjusted to 3 with 6 N HCI and it was extracted with EtOAc. The combined organic phases were dried over MgS0 4 , filtered and concentrated to dryness to afford the title compound (1.1 g, 78% yield).

Intermediate 17: tert- Butyl (3-((2-bromobenzyl)oxy)-3-phenylpropyl)(methyl)carbamate

To a solution of ferf-butyl (3-hydroxy-3-phenylpropyl)(methyl)carbamate (2 g, 7.5 mmol) and tetrabutylammonium iodide (2.8 g, 7.5 mmol) in DMF (10 mL), cooled at 0 °C under a N 2 atmosphere, NaH (60 wt% dispersion in mineral oil, 603 mg, 15 mmol) was added portionwise and the mixture was stirred at 0 °C for 30 min. Then a solution of 1-bromo- 2-(bromomethyl)benzene (1.8 g, 7.5 mmol) in DMF (4 mL) was added and the reaction mixture was stirred at r.t. overnight. Water and EtOAc were added, the phases were separated and the aqueous phase was extracted with EtOAc. The combined organic phases were washed with water and brine, dried over MgS0 4, filtered and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (2.34 g, 71 % yield).

Intermediate 18. tert-Butyl (3-(2-aminophenoxy)-3-phenylpropyl)(methyl)carbamate

Step 1. terf-Butyl methyl(3-(2-nitrophenoxy)-3-phenylpropyl)carbamate: Following the experimental procedure described in Step 1 of Intermediate 13, using terf-butyl (3- hydroxy-3-phenylpropyl)(methyl)carbamate and 2-nitrophenol as starting materials, the title compound was obtained (1.55 g, 63% yield).

Step 2. Title compound: To a solution of the compound obtained in Step 1 (1.55 g, 4 mmol) in a mixture of EtOH-water 4:1 (33 ml_), iron (2.2 g, 40 mmol) and ammonium chloride (107 mg, 2 mmol) were added and the mixture was heated to reflux for 4 h. It was allowed to cool down to r.t. and the suspension was filtered through a pad of Celite, that was washed with EtOH. The filtrate was concentrated to dryness to render the title compound that was used without further purification (1.24 g, 87% yield).

Intermediate 19: (S)-tert-Butyl (3-(2-bromophenoxy)-3- phenylpropyl)(methyl)carbamate

Step 1. (S)-3-(2-Bromophenoxy)-A/-methyl-3-phenylpropan-1 -amine: Following the experimental procedure described in Step 3 of Intermediate 6, using (S)-3- (methylamino)-1-phenylpropan-1 -ol as starting material, the title compound was obtained (1.76 g, 96% yield). Step 2. Title compound: Following the procedure described in Step 3 of Intermediate 13, starting from the product obtained in Step 1 , the title compound was obtained (314 mg, 26 % yield).

This method was used for the preparation of Intermediates 20-21 using suitable starting materials:

Intermediate 22: tert- Butyl methyl(3-(2-(2-oxoethyl)phenoxy)-3- phenylpropyl)carbamate

Step 1. tert- Butyl (3-(2-(2-hydroxyethyl)phenoxy)-3-phenylpropyl)(methyl)carbam ate: Following the experimental procedure described for the preparation of Intermediate 14, but using 2-(2-hydroxyethyl)phenol instead of 2-bromophenol, the title compound was obtained (1.51 g, 22% yield). Step 2. Title compound: To a solution of oxalyl chloride (0.77 mL, 4.31 mmol) in DCM (1 1 mL), cooled at -78 °C under a N 2 atmosphere, DMSO (0.61 mL, 8.62 mmol) was added. The solution was stirred for 5 min at -78 0 C, and then a solution of the compound obtained in Step 1 (1.51 g, 3.92 mmol) in DCM (1 1 mL) and TEA (1 .64 mL, 1 1 .75 mmol) were sequentially added. The reaction mixture was left to warm to r.t. during 1.5 h. Then, 1 N NaOH solution was added and it was extracted with DCM. The combined organic phases were washed with brine, dried over MgS0 4, filtered and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (628 mg, 42% yield).

Intermediate 23: Lithium 2-(3-((terf-butoxycarbonyl)(methyl)amino)-1 -(thiophen-2- yl)propoxy)benzoate

Step 1. Methyl 2-(3-((tert-butoxycarbonyl)(methyl)amino)-1 -(thiophen-2- yl)propoxy)benzoate: Following the procedure described in Step 1 of Intermediate 13, starting from tert-butyl (3-hydroxy-3-(thiophen-2-yl)propyl)(methyl)carbamate (1 .56 g, 5.74 mmol) and methyl 2-hydroxybenzoate (0.87 g, 5.74 mmol), the title compound was obtained (1.05 g, 45% yield).

Step 2. Title compound: Following the experimental procedure described in Step 2 of Intermediate 10, starting from the product obtained in Step 1 (105 mg, 0.26 mmol), the title compound was obtained (153 mg, overweight, quant yield).

Intermediate 24: 2-(Trimethylsilyl)ethyl (1 -(2-(2-bromophenoxy)-2-(thiophen-2- yl)ethyl)cyclopropyl)(methyl)carbamate

Step 1. terf-Butyl methyl(1 -((2-(thiophen-2-yl)-1 ,3-dithian-2- yl)methyl)cyclopropyl)carbamate: A solution of 2-(thiophen-2-yl)-1 ,3-dithiane (287 mg, 1 .42 mmol) in dry THF (3.2 ml_), cooled at -35 °C under a N 2 atmosphere, BuLi (1.6 M solution in hexanes, 1 .1 ml_, 1.7 mmol) was added dropwise. The reaction mixture was stirred at -35 °C for 1 .5 h, then it was warmed to -10 °C and stirred at this temperature for 10 min. The mixture was again cooled to -35 °C and a solution of terf-butyl (1 - (bromomethyl)cyclopropyl)(methyl)carbamate (450 mg, 1.7 mmol) in dry THF (1 .5 mL) was added. The reaction mixture was then stirred at r.t. overnight. Water and NH 4 CI sat. solution were added and it was extracted with EtOAc. The combined organic phases were washed with brine, dried over MgS0 4, filtered and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient CH to EtOAc, to give the title compound (352 mg, 64% yield).

Step 2. terf-Butyl methyl(1 -(2-oxo-2-(thiophen-2-yl)ethyl)cyclopropyl)carbamate: To a solution of the product obtained in Step 1 (350 mg, 0.9 mmol) in a mixture of ACN (2 mL) and NaHC0 3 sat. solution (2 mL), cooled at 0 °C, iodine (921 mg, 3.63 mmol) was added portionwise. The reaction mixture was vigorously stirred and left to warm to r.t. for 1 h. Na 2 S 2 C>3 sat. solution was added to eliminate residual iodine and it was extracted with EtOAc. The combined organic phases were washed with brine, dried over MgS0 4, filtered and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (175 mg, 65% yield).

Step 3. 2-(1 -(Methylamino)cyclopropyl)-1 -(thiophen-2-yl)ethanone hydrochloride: A solution of the product obtained in Step 2 (175 mg, 0.59 mmol) in a mixture of 1 ,4- dioxane (2 mL) and HCI (4 N solution in 1 ,4-dioxane) was stirred at r.t. overnight. The solvent was evaporated to dryness to obtain the title compound as a white solid (137 mg, quant yield).

Step 4. 2-(1 -(Methylamino)cyclopropyl)-1 -(thiophen-2-yl)ethanol: To a solution of the product obtained in Step 3 (137 mg, 0.59 mmol) in MeOH (5 mL), NaBH 4 (89 mg, 2.36 mmol) was added portionwise and the reaction mixture was stirred for 1 h at r.t.. NH 4 CI sat. solution was added, MeOH was evaporated and the pH of the aqueous phase was adjusted to 9-10 with 1 N NaOH solution. It was extracted with DCM and the combined organic phases were dried over MgS0 4 filtered and concentrated to dryness to afford the title compound (104 mg, 89% yield).

Step 5. 1 -(2-(2-Bromophenoxy)-2-(thiophen-2-yl)ethyl)-/\/-methylcyclo propanamine: Following the experimental procedure described in Step 2 of Intermediate 1 , starting from the product obtained in Step 4, the title compound was obtained (94 mg, 50% yield).

Step 6. Title compound: Following the experimental procedure described in Step 3 of Intermediate 1 , starting from the product obtained in Step 5, the title compound was obtained (28 mg, 21 % yield).

Intermediate 25. 2-(Trimethylsilyl)ethyl (3-((2-formylbenzyl)oxy)-3-(thiophen-2- yl)propyl)(methyl)carbamate

Step 1. 2-((3-(Benzyl(methyl)amino)-1-(thiophen-2-yl)propoxy)methyl) benzonitrile: To a solution of 3-(benzyl(methyl)amino)-1-(thiophen-2-yl)propan-1-ol (400 mg, 1.53 mmol) in DMF (5 mL), cooled at 0 °C, NaH (60 wt% dispersion in mineral oil, 92 mg, 2.29 mmol) was added and the mixture was stirred at r.t. for 30 min. It was then cooled to 0 °C, 2-(bromomethyl)benzonitrile (360 mg, 1.83 mmol) was added and the reaction mixture was stirred at r.t. for 16 h. Water was added, it was extracted with DCM and the organic layer was concentrated under vacuum. The crude product was purified by flash chromatography, silica gel, gradient hexane to EtOAc to give the title compound (400 mg, 70% yield).

Step 2. 2-(Trimethylsilyl)ethyl (3-((2-cyanobenzyl)oxy)-3-(thiophen-2- yl)propyl)(methyl)carbamate: To a mixture of 2-(trimethylsilyl)ethanol (349 mg, 2.95 mmol) and K 2 C0 3 (679 mg, 4.91 mmol) in toluene (5 mL), cooled at 0 °C, a solution of triphosgene (292 mg, 0.98 mmol) in toluene (5 mL) was added dropwise and the mixture was stirred at r.t. for 1 h. The reaction mixture was then cooled at 0 °C, a solution of the product obtained in Step 1 (370 mg, 0.98 mmol) in toluene (5 mL) was added and it was stirred at r.t. for 16 h. NaHC0 3 sat. solution was added, it was extracted with EtOAc and the organic layer was concentrated under vacuum. The residue was purified by flash chromatography, silica gel, gradient hexane to EtOAc to give the title compound (135 mg, 32% yield).

Step 3. Title compound: To a solution of the product obtained in Step 2 (130 mg, 0.30 mmol) in toluene (2 mL), cooled at -78 °C, DIBAL-H (1 M solution in toluene, 0.45 mL, 0.45 mmol) was added. The mixture was stirred at -78°C for 30 min and then at r.t. for 1 h. MeOH was added dropwise and then 10% HCI aq. solution. It was extracted with EtOAc and the organic phase was dried over Na 2 S0 4 , filtered and concentrated to dryness to afford the title compound (60 mg, 46% yield) that was used in the next step without further purification.

Intermediate 26. tert- Butyl (3-chloro-3-(3-cyanophenyl)propyl)(methyl)carbamate

Step 1. 3-(3-(Methylamino)propanoyl)benzonitrile hydrochloride: Following the procedure described in Step 1 of Intermediate 6, using 3-acetylbenzonitrile as starting material, the title compound was obtained (1.31 g, 28% yield).

Step 2. 3-(1-Hydroxy-3-(methylamino)propyl)benzonitrile Following the experimental procedure described in Step 2 of Intermediate 6, starting from the product obtained in Step 1 , the title compound was obtained (0.81 g, 73% yield).

Step 3. 3-(1-Chloro-3-(methylamino)propyl)benzonitrile hydrochloride: To a cooled solution of the product obtained in Step 2 (0.81 g, 4.3 mmol) in DCM (2.5 ml_), a solution of SOC (0.34 ml_, 4.7 mmol) in DCM (1.3 mL) was added dropwise. The mixture was stirred at r.t. for 2 h and then the solvent was concentrated to dryness to render the title compound (978 mg, 93% yield). Step 4. Title compound: The crude product obtained in Step3 (0.98 g, 3.9 mmol) was dissolved in tert- butanol (3.9 ml_). Water (3.9 mL), 6 M NaOH solution (0.86 ml_, 5.2 mmol) and di-terf-butyl dicarbonate (0.96 g, 4.4 mmol) were added and the reaction mixture was stirred at r.t. for 15 min. Brine and DCM were added, the phases were separated and the aqueous layer was extracted with DCM. The combined organic phases were washed with brine, dried with Na 2 S0 4 and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :9) to give the title compound (875 mg, 71 % yield).

Intermediate 27. (f?)-(2-(Trimethylsilyl)ethyl 3-(2-bromophenoxy)-3- phenylpropyl)(ethyl)carbamate

This intermediate was prepared following the experimental procedure described for the preparation of Intermediate 1 , using suitable starting materials.

Intermediate 28. 2-(Trimethylsilyl)ethyl (3-(2-bromophenoxy)-3-(3- fluorophenyl)propyl)(ethyl)carbamate

Step 1. 3-(Ethylamino)-1-(3-fluorophenyl)propan-1-one hydrochloride: In a sealed tube, 1-(3-fluorophenyl)ethan-1-one (5.0 g, 36.2 mmol), ethylamine hydrochloride (3.54 g, 43.4 mmol) and paraformaldehyde (1.52 g, 50.7 mmol) were dissolved in EtOH (40 mL) and the mixture was heated at 110 °C for 9 h. The solvent was evaporated, EtOAc (40 mL) was added and the suspension was stirred at r.t. for 1 h. The solids were filtered, washed with EtOAc and dried under vacuum, to afford the title compound (4.84 g, 49% yield).

Step 2. 3-(Ethylamino)-1-(3-fluorophenyl)propan-1-ol: Following the experimental procedure described in Step 2 of Intermediate 6, using the product obtained in Step 1 as starting material, the title compound was obtained (2.1 g, 60% yield).

Step 3. 3-(2-Bromophenoxy)-/\/-ethyl-3-(3-fluorophenyl)propan-1 -amine: Following the experimental procedure described in Step 2 of Intermediate 1 , using the product obtained in Step 2 instead of (R)-3-(ethylamino)-1-(thiophen-2-yl)propan-1-ol, the title compound was obtained (6.71 g, 56 wt%, quant yield assumed).

Step 4. Title compound: Following the experimental procedure described in Step 3 of Intermediate 1 , using the product obtained in Step 3 as starting material, the title compound was obtained (2.74 g, 29% yield).

Synthesis of Examples

General Deprotection Methods

Method 1. Boc deprotection with TMSI. To a solution of the N- Boc protected compound (1 mmol) in dry ACN (45 mL), TMSI (2 mmol) was added dropwise. After stirring for 15 min at r.t., NaHC0 3 sat. solution and DCM were added and the mixture was stirred for additional 10 minutes. The phases were separated, the organic phase was dried over MgS0 4 and concentrated to dryness, to afford the crude compound, which was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4). Method 2. Boc deprotection with TFA. A solution of the A/-Boc protected compound (1 mmol) in a mixture of DCM (15 ml_) and TFA (10 mmol) was stirred at r.t. until full conversion was achieved. The volatiles were evaporated and the residue was re- dissolved in DCM and washed with 1 M NaOH solution and brine, dried over MgS0 4 and concentrated. The crude compound was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4).

Method 3. Boc deprotection with HCI. To a solution of the N-Boc protected compound (1 mmol) in dioxane (10 ml_), HCI (4 N solution in dioxane, 10 mmol) was added under a N 2 atmosphere. The reaction was stirred at r.t. overnight. The solvent was evaporated and the residue was purified by eluting through an acidic ion exchange resin cartridge (SCX), to give the desired compound, which was further purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4).

Method 4. Teoc deprotection with CsF. A solution of the A/-Teoc protected compound (1 mmol) and cesium fluoride (5 mmol) in DMF (26 ml_) was heated at 90 °C for 1 h. The solvent was concentrated to dryness and the crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4).

Example 1 : (R)-A/-Ethyl-1-(2-(3-(methylamino)-1-(thiophen-2-yl)propoxy) phenyl)-4- phenylpiperidin-4-amine

Step 1. (f?)-2-(Trimethylsilyl)ethyl (3-(2-(4-(ethylamino)-4-phenylpiperidin-1- yl)phenoxy)-3-(thiophen-2-yl)propyl)(methyl)carbamate: In a sealed tube, a mixture of Intermediate 3 (100 mg, 0.213 mmol), A/-ethyl-4-phenylpiperidin-4-amine (52 mg, 0.255 mmol), Pd2(dba) 3 (20 mg, 0.021 mmol), BINAP (43 mg, 0.043 mmol) and sodium tert- butoxide (61 mg, 0.638 mmol) in dry toluene (4 mL) was heated at 130 °C overnight under an argon atmosphere. The reaction mixture was filtered through a pad of Celite, that was washed with EtOAc, and the filtrates were concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (57 mg, 45% yield).

Step 2. Title compound: Starting from the compound obtained in Step 1 (57 mg, 0.096 mmol) and following General Deprotection Method 4, the title compound was obtained (34 mg, 79% yield).

HPLC retention time (method B): 5.93 min; MS: 450.2 (M+H).

This method was used for the preparation of Examples 2-22 using suitable starting materials:

Cj

Example 23: (R)-2-(4-(Dimethylamino)-4-phenylpiperidin-1 -yl)-/V-(2-(3-((2- fluoroethyl)amino)-1-(thiophen-2-yl)propoxy)phenyl)acetamide

Step 1. 2-(4-(Dimethylamino)-4-phenylpiperidin-1-yl)acetamide: A mixture of N,N- dimethyl-4-phenylpiperidin-4-amine dihydrochloride (1.5 g, 5.41 mmol), 2- bromoacetamide (0.8 g, 5.79 mmol), Kl (90 mg, 0.54 mmol) and K 2 CO 3 (2.24 g, 16.23 mmol) in ACN (50 ml.) was heated at 50 °C overnight. The suspension was filtered, the collected solids were washed with ACN and discarded, and the filtrate was concentrated to dryness to afford the title compound (1.5 g, quant yield), which was used without further purification.

Step 2. (R)-2-(T rimethylsilyl)ethyl (3-(2-(2-(4-(dimethylamino)-4-phenylpiperidin-1- yl)acetamido)phenoxy)-3-(thiophen-2-yl)propyl)(2-fluoroethyl )carbamate: In a sealed tube, a mixture of Intermediate 5 (153 mg, 0.304 mmol), the product obtained in Step 1 (1 11 mg, 0.414 mmol), AT./^-dimethylethane-l ,2-diamine (0.01 mL, 0.091 mmol), copper(l) iodide (17 mg, 0.091 mmol) and potassium phosphate (129 mg, 0.609 mmol) in 1 ,4-dioxane (5 mL) was heated at 120 °C overnight under an argon atmosphere. It was filtered through a pad of Celite, that was washed with DCM, and the filtrate was concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (170 mg, 82% yield).

Step 3. Title compound: Starting from the compound obtained in Step 2 (170 mg, 0.249 mmol) and following General Deprotection Method 4, the title compound was obtained (105 mg, 78% yield).

HPLC retention time (method B): 5.44 min; MS: 538.9 (M+H).

This method was used for the preparation of Examples 24-30 using suitable starting materials:

Example 31 : 1-(2-(3-(Dimethylamino)-1-(thiophen-2-yl)propoxy)benzyl)-/\/ ,A/-dimethyl- 4-phenylpiperidin-4-amine

Step 1. 1-(2-(3-Chloro-1-(thiophen-2-yl)propoxy)benzyl)-A/,/V-dimeth yl-4- phenylpiperidin-4-amine: A solution of Intermediate 8 (350 mg, 1.25 mmol), N,N- dimethyl-4-phenylpiperidin-4-amine dihydrochloride (255 mg, 1.25 mmol) and DIPEA (0.434 ml_, 2.49 mmol) in DCE (7 mL) was stirred for 30 min at r.t. under a N 2 atmosphere. Then, sodium triacetoxyborohydride (526 mg, 2.49 mmol) was added and the reaction mixture was stirred at r.t. overnight. NaHCC>3 sat. solution was added and it was extracted with DCM. The combined organic phases were washed with brine, dried over Na 2 S0 4 and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (225 mg, 38% yield).

Step 2. Title compound: A solution of the compound obtained in Step 1 (184 mg, 0.39 mmol) and dimethylamine (33 wt% solution in EtOH, 4.2 mL, 23.54 mmol) was heated in a sealed tube at 100 °C for 20 h. The solvent was evaporated to dryness and the crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (191 mg, quantitative yield).

HPLC retention time (method B): 6.56 min; MS: 478.3 (M+H).

This method was used for the preparation of Examples 32-45 using suitable starting materials:

Example 46: A/,/V-Dimethyl-1 -(2-(3-(methylamino)-1-phenylpropoxy)benzyl)-4- phenylpiperidin-4-amine

Step 1. ferf-Butyl (3-(2-((4-(dimethylamino)-4-phenylpiperidin-1 -yl)methyl)phenoxy)-3- phenylpropyl)(methyl)carbamate: Following the experimental procedure described in Step 1 of Example 31 , starting from Intermediate 15 (77 mg, 0.21 mmol) and N,N- dimethyl-4-phenylpiperidin-4-amine dihydrochloride (43 mg, 0.21 mmol), the title compound was obtained (14 mg, 12% yield).

Step 2. Title compound: Starting from the compound obtained in Step 1 (14 mg, 0.025 mmol) and following General Deprotection Method 2, the title compound was obtained (8 mg, 70% yield).

HPLC retention time (method A): 4.41 min; MS: 458.3 (M+H). This method was used for the preparation of Examples 47-48 using suitable starting materials:

Example 49: 1 -(4-(Dimethylamino)-4-phenylpiperidin-1 -yl)-3-(2-(3-(methylamino)-1 - (thiophen-2-yl)propoxy)phenyl)propan-1-one

Step 1. 3-(2-(3-Chloro-1-(thiophen-2-yl)propoxy)phenyl)-1-(4-(dimeth ylamino)-4- phenylpiperidin-1-yl)propan-1-one: To a solution of Intermediate 12 (150 mg, 0.46 mmol) and A/,A/-dimethyl-4-phenylpiperidin-4-amine (94 mg, 0.46 mmol) in dry DMF (4.5 ml_), DIPEA (0.241 mL, 1.39 mmol) and HATU (175 mg, 0.46 mmol) were added and the reaction mixture was stirred at r.t. overnight. NaHCC>3 sat. solution was added and it was extracted with EtOAc. The combined organic phases were washed with water and brine, dried over MgSC and concentrated to dryness. The crude product thus obtained (221 mg, 94% yield) was used without further purification.

Step 2. Title compound: Following the experimental procedure described in Step 2 of Example 31 , starting from the product obtained in Step 1 (221 mg, 0.43 mmol) and methylamine, the title compound was obtained (25 mg, 11 % yield).

HPLC retention time (method B): 5.64 min; MS: 506.2 (M+H).

This method was used for the preparation of Examples 50-52 using suitable starting materials:

Example 53: (4-(Dimethylamino)-4-phenylpiperidin-1 -yl)(2-(3-(methylamino)-1 - phenylpropoxy)phenyl)methanone

Step 1. tert- Butyl (3-(2-(4-(dimethylamino)-4-phenylpiperidine-1-carbonyl)pheno xy)-3- phenylpropyl)(methyl)carbamate: Following the experimental procedure described in Step 1 of Example 49, using Intermediate 16 (94 mg, 0.24 mmol) as starting material, the title compound was obtained (64 mg, 46% yield). Step 2. Title compound: Starting from the compound obtained in Step 1 (64 mg, 0.11 mmol) and following General Deprotection Method 3, the title compound was obtained (19 mg, 32% yield).

HPLC retention time (method A): 4.71 min; MS: 472.2 (M+H).

This method was used for the preparation of Example 54 using suitable starting materials:

Example 55: 2-(4-(Dimethylamino)-4-phenylpiperidin-1 -yl)-/V-(2-(3-(methylamino)-1 - phenylpropoxy)phenyl)acetamide

Step 1. tert- Butyl (3-(2-(2-chloroacetamido)phenoxy)-3- phenylpropyl)(methyl)carbamate: To a solution of Intermediate 18 (600 mg, 1.68 mmol) in ACN (8 mL), under a N 2 atmosphere, DIPEA (0.733 ml_, 4.2 mmol) and 2- chloroacetyl chloride (0.16 ml_, 2.02 mmol) were added dropwise. The mixture was stirred for 1 h at r.t. and then it was concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient CH to EtOAc to give the title compound (562 mg, 77% yield). Step 2. terf-Butyl (3-(2-(2-(4-(dimethylamino)-4-phenylpiperidin-1- yl)acetamido)phenoxy)-3-phenylpropyl)(methyl)carbamate: A solution of the product obtained in Step 1 (100 mg, 0.23 mmol), /V,A/-dimethyl-4-phenylpiperidin-4-amine (1 12 mg, 0.56 mmol) and DIPEA (0.1 mL) in EtOH (10 mL) was heated in a sealed tube at 80 °C for 3 days. The solvent was evaporated and the residue was dissolved in EtOAc. The organic phase was washed with 1 N NaOH solution, dried over MgS0 4 and concentrated to dryness. The crude product thus obtained (133 mg, quantitative yield) was used without further purification.

Step 3. Title compound: Following General Deprotection Method 2, starting from the compound obtained in Step 2 (133 mg, 0.23 mmol), the title compound was obtained (59 mg, 51 % yield).

HPLC retention time (method A): 4.66 min; MS: 501.3 (M+H).

Example 56: 3-(1 -(2-(4-(Dimethylamino)-4-phenylpiperidin-1 -yl)phenoxy)-3-

(methylamino)propyl)benzonitrile

Step 1. 1-(2-Methoxyphenyl)-A/,A/-dimethyl-4-phenylpiperidin-4-amine : Following the experimental procedure described in Step 1 of Example 1 , using 1 -bromo-2- methoxybenzene (57 mg, 0.31 mmol) and A/,A/-dimethyl-4-phenylpiperidin-4-amine dihydrochloride (100 mg, 0.36 mmol) as starting materials, the title compound was obtained (1 1 1 mg, overweight, quant yield).

Step 2. 2-(4-(Dimethylamino)-4-phenylpiperidin-1 -yl)phenol: To a solution of the compound obtained in Step 1 (1 1 1 mg, 85 wt%, 0.31 mmol) in DCM (2.2 mL), cooled at -78 °C under a N 2 atmosphere, boron tribromide (1 M solution in DCM, 1.8 mL, 1.8 mmol) was added. The reaction mixture was then stirred at -20 °C for 2 h. Water was carefully added, the pH of the mixture was adjusted to 9 with 1 N NaOH solution and it was extracted with DCM. The combined organic phases were washed with brine, dried over Na 2 S04 and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4, containing 3% NH4OH) to give the title compound (33 mg, 37% yield).

Step 3. tert-Butyl (3-(3-cyanophenyl)-3-(2-(4-(dimethylamino)-4-phenylpiperidin -1 - yl)phenoxy)propyl)(methyl)carbamate: In a sealed tube, a mixture of Intermediate 26 (34 mg, 0.1 1 mmol), the product obtained in Step 2 (33 mg, 0.11 mmol), K 2 C0 3 (46 mg, 0.33 mmol) and Kl (2 mg, 0.01 mmol) in DMF (0.8 mL) was heated at 60 °C overnight. The solvent was removed under vacuum and the residue was partitioned between water and EtOAc. The aqueous phase was extracted with EtOAc and the combined organic phases were washed with 1 N NaOH solution and brine, dried over Na 2 S0 4 and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (21 mg, 33% yield).

Step 4. Title compound: Following General Deprotection Method 2, starting from the compound obtained in Step 3 (21 mg, 0.037 mmol), the title compound was obtained (2 mg, 1 1 % yield).

HPLC retention time (method A): 4.35 min; MS: 469.3 (M+H).

Example 57. ( R)-N , A/-Dimethyl-1 -(2-(3-(methylamino)-1 -(thiophen-2- yl)propoxy)benzyl)-4-phenylpiperidin-4-amine

Step 1. ((4-(Dimethylamino)-4-phenylpiperidin-1 -ium-1-yl)methyl)trifluoroborate: A schlenk flask was loaded with potassium (bromomethyl)trifluoroborate (26 mg, 1.29 mmol) and A/,A/-dimethyl-4-phenylpiperidin-4-amine (220 mg, 1 .07 mmol) and then it was evacuated and backfilled with argon three times. A mixture of THF-BuOH 2: 1 (5.7 ml_, degassed by bubbling argon through) was added and the resulting solution was heated at 80 °C overnight. The solvent was concentrated to dryness and the residue was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (209 mg, 68% yield).

Step 2. (R)-2-(Trimethylsilyl)ethyl (3-(2-((4-(dimethylamino)-4-phenylpiperidin-1 - yl)methyl)phenoxy)-3-(thiophen-2-yl)propyl)(methyl)carbamate : In a sealed tube, a mixture of Intermediate 3 (130 mg, 0.27 mmol), the product obtained in Step 1 (103 mg, 0.36 mmol), Pd(OAc)2 (1 1 mg, 0.05 mmol), XPhos (47 mg, 0.10 mmol) and CS2CO3 (270 mg, 0.83 mmol) in a mixture of 1 ,4-dioxane-water (10:1 , 2 mL) was heated at 1 10 °C overnight under an argon atmosphere. The solvent was concentrated and the residue was partitioned between EtOAc and NaHCC sat. solution. The phases were separated and the aqueous phase was extracted with EtOAc. The combined organic phases were washed with brine, dried over MgS0 4 and concentrated to dryness. The crude product was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1 :4) to give the title compound (1 14 mg, 68% yield).

Step 3. Title compound: Following General Deprotection Method 4, starting from the compound obtained in Step 2 (1 14 mg, 0.19 mmol), the title compound was obtained (60 mg, 69% yield).

HPLC retention time (method B): 5.15 min; MS: 464.1 (M+H). This method was used for the preparation of Example 58 using suitable starting materials:

Following the method described for the preparation of Example 1 but using suitable starting materials, Examples 59-65 were obtained:

Examples 66 and 67: (f?)-1-(2-(3-(Ethylamino)-1-(3-fluorophenyl)propoxy)phenyl)- /V- methyl-4-phenylpiperidin-4-amine and (S)-1 -(2-(3-(ethylamino)-1 -(3- fluorophenyl)propoxy)phenyl)-/V-methyl-4-phenylpiperidin-4-a mine

Starting from Example 65, a chiral preparative HPLC separation (column: Chiralcel ADH; temperature: ambient; flow: 12 mL/min; eluent: n-Heptane/IPA 70:30 v/v) was carried out to give the title compounds.

Table of Examples with binding to the u-opioid Receptor and the a 2 d-1 Subunit of the voltage-gated calcium channel:

BIOLOGICAL ACTIVITY

Pharmacological study Human a 2 d-1 subunit of Ca v 2.2 calcium channel assay

Human a 2 d-1 enriched membranes (2.5 pg) were incubated with 15 nM of radiolabeled [3H]-Gabapentin in assay buffer containing Hepes-KOH 10mM, pH 7.4. NSB (non specific binding) was measured by adding 10 pM pregabalin. The binding of the test compound was measured at five different concentrations. After 60 min incubation at 27 °C, binding reaction was terminated by filtering through Multiscreen GF/C (Millipore) presoaked in 0.5 % polyethyleneimine in Vacuum Manifold Station, followed by 3 washes with ice-cold filtration buffer containing 50 mM Tris-HCI, pH 7.4. Filter plates were dried at 60 °C for 1 hour and 30 pi of scintillation cocktail were added to each well before radioactivity reading. Readings were performed in a Trilux 1450 Microbeta radioactive counter (Perkin Elmer).

Human u-opioid receptor radioligand assay

Transfected CHO-K1 cell membranes (20 pg) were incubated with [ 3 H]-DAMGO (1 nM) in assay buffer containing Tris-HCI 50 mM, MgCI 2 5 mM at pH 7.4. NBS (non-specific binding) was measured by adding 10 mM Naloxone. The binding of the test compound was measured at five different concentrations. Plates were incubated at 27 °C for 60 min. After the incubation period, the reaction mixture was then transferred to Multiscreen HTS, FC plates (Millipore), filtered and plates were washed 3 times with ice-cold 10 mM T ris-HCI (pH 7.4). Filters were dried and counted at approximately 40% efficiency in a MicroBeta scintillation counter (Perkin-Elmer) using EcoScint liquid scintillation cocktail.

Results:

As this invention is aimed at providing a compound or a chemically related series of compounds which act as dual ligands of the 0126 subunit of voltage-gated calcium channels and the p-opioid receptor it is a very preferred embodiment in which the compounds are selected which act as dual ligands of the a 2 d subunit of voltage-gated calcium channels and the m-opioid receptor and especially compounds which have a binding expressed as Ki responding to the following scales:

Kί(m) is preferably < 1000 nM, more preferably < 500 nM, even more preferably < 100 nM.

Kί(a2d-1 ) is preferably < 10000 nM, more preferably < 5000 nM, or even more preferably < 500 nM.

The following scale has been adopted for representing the binding to m-opioid receptor expressed as :

+ Ki (m) >= 500 nM

++ 100 nM <= Kί(m) < 500 nM

+++ Kϊ(m) < 100 nM

The following scale has been adopted for representing the binding to the a2d-1 subunit of voltage-gated calcium channels expressed as Ki:

+ Kί(a 2 d-1) >= 5000 nM

++ 500nM <= Kί(a 2 d-1) <5000 nM

+++ Ki(a 2 d-1) <500 nM

All compounds prepared in the present application exhibit binding to the a2d-1 subunit of voltage-gated calcium channels and the m-opioid receptor, in particular the following binding results are shown: