TEAD INHIBITORS Technical field The present invention relates to therapeutically active compounds useful in the inhibition of transcriptional enhancer associate domain (TEAD), and to pharmaceutical compositions containing such compounds. The compounds are useful in the treatment of diseases or disorders associated with increased TEAD activity or TEAD expression, such as various cancers and chronic pain. Background of the invention TEA domain transcription factors (TEAD1-4) is a family of DNA binding transcription factors which regulate the expression of genes involved in cell proliferation, cell fate, cell differentiation, organ overgrowth and organ regeneration. YAP and TAZ are TEAD transcriptional co-activators which can shuttle between the cytoplasm and the nucleus. Altered actin dynamics and the Hippo signalling pathway promote YAP and TAZ phosphorylation, cytoplasmic retention and proteasomal degradation, consequently leading to low YAP and TAZ nuclear levels and TEAD transcriptional activity. The evolutionarily conserved Hippo signalling pathway is consisting of the large tumor suppressor 1/2 (LATS1/2), the serine/threonine kinases, sterile 20-like kinase 1/2 (MST1/2), and the adaptor proteins Salvador homolog 1 (SAV1) and MOB kinase activator 1A/B (MOB1A/B). The tumor suppressor neurofibromin 2 (NF2) (also known as Merlin) participates upstream of these kinases to inhibit YAP and TAZ activity by promoting the activation of the pathway. The Hippo pathway has been linked to many aspects of tumorigenesis, including cell proliferation, cell differentiation, cancer metastasis and cancer therapy resistance. Therefore, dysregulation in Hippo pathway signalling has been shown to drive oncogenesis across various cancer types. It has also been reported that YAP and TAZ are core mechanisms underlying the pathogenesis of chronic pain, such as chronic neuropathic pain and chronic musculoskeletal pain. Compounds with TEAD inhibition activity have been disclosed, for example, in WO 2020/081572, WO 2020/070181 and WO 2020051099. Anti-tumor effects of a TEAD inhibitor, K-975, in vivo on malignant pleural mesothelioma has been reported in Am J Cancer Res, 2020; 10(12): 4399-4415. There is a need for compounds targeting diseases associated with dysregulation in the Hippo pathway components, for example compounds targeting the YAP-TEAD interaction. Such compounds would be useful for the treatment of diseases or conditions wherein inhibition of TEAD is desired, such as chronic pain including neuropathic pain and various cancers including cancers which are resistant to other treatments, such as chemotherapy, immunotherapy and targeted therapies. Summary of the invention It has been found that compounds of formula (I) are potent inhibitors of YAP- TEAD interaction. The compounds are therefore useful for the treatment of conditions and diseases where inhibition of TEAD is desired. Such conditions and diseases include, but are not limited to, chronic pain, particularly chronic neuropathic pain and chronic musculoskeletal pain, and cancers, particularly cancers associated with dysregulation in the Hippo pathway components including YAP-TEAD. Particular cancers include, but are not restricted to, mesothelioma, squamous cell carcinomas, gynaecological cancers, bladder cancer, gastric cancer, liver cancer, lung cancer and colon cancer. The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein A is pyridyl, tetrahydropyranyl, a 4-10 membered carbocyclic ring; L is -O-, -S-, -NH-, -C _1-7 alkyl-, -C _2-7 alkenyl-, -C _1-7 alkyl-O-, -O-C _1-7 alkyl- or -NH-C _1-7 alkyl-; R ₁ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, hydroxyl, cyano, -C(O)NR ₃₆ R ₃₇ , or an optionally substituted 5-6 membered heterocyclic ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; R ₂ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy or halogen; R ₃ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl or cyano, or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₄ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, cyano or C _1-7 alkylcarbonyl; R ₅ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, nitro, amino, hydroxyl, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, or R ₄ and R ₅ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; Z is –CH(NHR ₂₅ )-(CH ₂ ) ₂ -COOH or a group of formula wherein B is any one of the following groups

; provided that when B is ring (2), then L is -O- or -O-C _1-7 alkyl-, and R ₁ is C _1-7 alkoxy; when B is ring (3), then L is -O-; when B is ring (4), then L is -O- and R ₁ is C _1-7 alkoxy; when B is ring (20), (21), (23), (25) or (26), then L is -O- and R ₁ is C _1-7 alkoxy; when L is -C _1-7 alkyl-O-, then R ₁ is C _1-7 alkoxy or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; when A is a 4-, 5-, 7-, 8-, 9- or 10-membered carbocyclic ring, then R ₁ is C _1-7 alkoxy; R6 and R9 are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, C _3-7 cyclo- alkyl C _1-7 alkyl, -C(O)-RX, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkoxycarbonyl C _1-7 alkyl, -SO ₂ C _1-7 alkyl, -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; RX is C _1-7 alkyl, C _3-7 cycloalkyl, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkyl-NR ₃₆ R ₃₇ , or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₇ , R ₈ , R ₁₀ , R ₁₂ , R ₁₃ , R ₁₄ , R ₁₅ , R ₁₆ , R ₁₇ , R ₁₈ , R ₁₉ , R ₂₀ , R ₂₁ , R ₂₂ and R ₂₆ are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, hydroxyl, C _1-7 alkoxy or C _1-7 alkylcarbonyl; R ₁₁ is hydrogen, C _1-7 alkyl, halogen C _1-7 alkyl or C _1-7 alkylcarbonyl; R ₂₃ , R ₂₄ , R ₂₇ , R ₂₈ , R ₂₉ , R ₃₁ , R _32, R ₃₃ , R _34, R _35, R _36, R ₃₇ , R ₄₀ , R ₄₁ , R ₄₂ , R _43, R _44, and R ₄₅ are, independently, hydrogen, or C _1-7 alkyl; R ₂₅ is C _1-7 alkyl; R ₃₀ is C _1-7 alkyl, C _1-7 alkylcarbonyl or -SO ₂ C _1-7 alkyl; R ₃₈ is hydrogen, C _1-7 alkyl, C _1-7 alkylcarbonyl, C _1-7 alkoxy C _1-7 alkylcarbonyl or -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ ; R ₃₉ is hydrogen, C _1-7 alkyl or hydroxyl; wherein optional substitution, in each occurrence, is 1-2 substituents independently selected from C _1-7 alkyl, halogen, halogen C _1-7 alkyl, C _1-7 alkoxy and oxo; with the proviso that compound of formula (I) is not N-[2-Methyl-3-(phenoxymethyl)phenyl]-5-oxo-2-pyrrolidinecarb oxamide; N-[5-[(3-Fluorophenoxy)methyl]-2-methoxyphenyl]-1-methyl-5-o xo-2- pyrrolidinecarboxamide; N-[3-[(4-Chlorophenyl)methyl]phenyl]-5-oxo-2-pyrrolidinecarb oxamide; N-[3-[(Cyclohexyloxy)methyl]phenyl]-1-methyl-5-oxo-2-pyrroli dine- carboxamide; N-[4-Methyl-3-[(4-methyl-2-pyridinyl)oxy]phenyl]-5-oxo-2-pyr rolidine- carboxamide; N-[3-(Cyclopentylamino)phenyl]-1-methyl-5-oxo-2-pyrrolidinec arboxamide; N-[3-[[(3-Methylcyclohexyl)oxy]methyl]phenyl]-6-oxo-3-piperi dine- carboxamide; 1-Ethyl-5-oxo-N-(3-phenoxyphenyl)-3-pyrrolidinecarboxamide; N-[5-[(3-Fluorophenoxy)methyl]-2-methoxyphenyl]-2-pyrrolidin ecarboxamide; 1-(1-Ethylpropyl)-N-[5-[(3-fluorophenoxy)methyl]-2-methoxyph enyl]-5-oxo-3- pyrrolidinecarboxamide; N-[3-[(4-Chlorophenyl)methyl]phenyl]-1,6-dihydro-6-oxo-3-pyr idine- carboxamide; 1,6-Dihydro-N-[4-methoxy-3-(phenylmethyl)phenyl]-6-oxo-3-pyr idine- carboxamide; 1,6-Dihydro-6-oxo-N-[3-[2-(2-pyridinyl)ethenyl]phenyl]-3- pyridinecarboxamide; N-[3-[(3-Fluorophenoxy)methyl]phenyl]-2,3-dihydro-2-oxo-1H-i midazole-4- carboxamide; 1-Methyl-N-[2-methyl-3-(phenoxymethyl)phenyl]-5-oxo-3-pyrrol idine- carboxamide; N-[3-[(1,3-Benzodioxol-5-yloxy)methyl]phenyl]-1-(2-methylpro pyl)-5-oxo-3- pyrrolidinecarboxamide; 1,6-Dihydro-N-[3-[[(3-methylcyclohexyl)oxy]methyl]phenyl]-6- oxo-3-pyridine- carboxamide; N-[3-[(Cyclohexyloxy)methyl]phenyl]-1-ethyl-5-oxo-3-pyrrolid inecarboxamide; 1-Methyl-N-[3-[[(3-methylcyclohexyl)oxy]methyl]phenyl]-5-oxo -3-pyrrolidine- carboxamide; 2,3-Dihydro-3-methyl-N-[3-[[(3-methylcyclohexyl)oxy]methyl]p henyl]-2-oxo- 1H-imidazole-4-carboxamide; 2,3-Dihydro-1,3-dimethyl-N-[3-[[(3-methylcyclohexyl)oxy]meth yl]phenyl]-2- oxo-1H-imidazole-4-carboxamide; 1-Ethyl-N-[4-methoxy-3-(4-pyridinylmethoxy)phenyl]-5-oxo-3-p yrrolidine- carboxamide; N-[4-Methoxy-3-(4-methoxyphenoxy)phenyl]-1-(2-methylpropyl)- 5-oxo-3- pyrrolidinecarboxamide or 6-Oxo-N-(3-phenoxyphenyl)-2-piperazinecarboxamide. According to one embodiment, the invention provides a method for the treatment of a disease or condition wherein inhibition of TEAD is desired comprising administering to a subject in need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof

wherein A is pyridyl, tetrahydropyranyl, a 4-10 membered carbocyclic ring; L is -O-, -S-, -NH-, -C _1-7 alkyl-, -C _2-7 alkenyl-, -C _1-7 alkyl-O-, -O-C _1-7 alkyl- or -NH-C _1-7 alkyl-; R ₁ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, hydroxyl, cyano, -C(O)NR ₃₆ R ₃₇ , or an optionally substituted 5-6 membered heterocyclic ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; R ₂ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy or halogen; R ₃ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl or cyano, or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₄ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, cyano or C _1-7 alkylcarbonyl; R ₅ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, nitro, amino, hydroxyl, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, or R ₄ and R ₅ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; Z is –CH(NHR ₂₅ )-(CH ₂ ) ₂ -COOH or a group of formula wherein B is any one of the following groups

provided that when B is ring (2), then L is -O- or -O-C _1-7 alkyl-, and R ₁ is C _1-7 alkoxy; when B is ring (3), then L is -O-; when B is ring (4), then L is -O- and R ₁ is C _1-7 alkoxy; when B is ring (20), (21), (23), (25) or (26), then L is -O- and R ₁ is C _1-7 alkoxy; when L is -C _1-7 alkyl-O-, then R ₁ is C _1-7 alkoxy or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; when A is a 4-, 5-, 7-, 8-, 9- or 10-membered carbocyclic ring, then R ₁ is C _1-7 alkoxy; R6 and R9 are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, C _3-7 cyclo- alkyl C _1-7 alkyl, -C(O)-RX, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkoxycarbonyl C _1-7 alkyl, -SO ₂ C _1-7 alkyl, -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; RX is C _1-7 alkyl, C _3-7 cycloalkyl, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkyl-NR ₃₆ R ₃₇ , or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₇ , R ₈ , R ₁₀ , R ₁₂ , R ₁₃ , R ₁₄ , R ₁₅ , R ₁₆ , R ₁₇ , R ₁₈ , R ₁₉ , R ₂₀ , R ₂₁ , R ₂₂ and R ₂₆ are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, hydroxyl, C _1-7 alkoxy or C _1-7 alkylcarbonyl; R ₁₁ is hydrogen, C _1-7 alkyl, halogen C _1-7 alkyl or C _1-7 alkylcarbonyl; R ₂₃ , R ₂₄ , R ₂₇ , R ₂₈ , R ₂₉ , R ₃₁ , R _32, R ₃₃ , R _34, R _35, R _36, R ₃₇ , R ₄₀ , R ₄₁ , R ₄₂ , R _43, R _44, and R ₄₅ are, independently, hydrogen, or C _1-7 alkyl; R ₂₅ is C _1-7 alkyl; R ₃₀ is C _1-7 alkyl, C _1-7 alkylcarbonyl or -SO ₂ C _1-7 alkyl; R ₃₈ is hydrogen, C _1-7 alkyl, C _1-7 alkylcarbonyl, C _1-7 alkoxy C _1-7 alkylcarbonyl or -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ ; R ₃₉ is hydrogen, C _1-7 alkyl or hydroxyl; wherein optional substitution, in each occurrence, is 1-2 substituents independently selected from C _1-7 alkyl, halogen, halogen C _1-7 alkyl, C _1-7 alkoxy and oxo. According to one embodiment, the disease or condition wherein inhibition of TEAD is desired is cancer, for example mesothelioma, squamous cell carcinoma, a gynaecological cancer, bladder cancer, gastric cancer, liver cancer, lung cancer and colon cancer. According to one embodiment, the disease or condition wherein inhibition of TEAD is desired is chronic pain, for example chronic neuropathic pain and chronic musculoskeletal pain. According to one embodiment, the invention provides a pharmaceutical composition comprising a compound of formula (I) together with a pharmaceutically acceptable carrier. Detailed description of the invention The present application provides novel compounds of formula (I) or pharmaceutically acceptable salts thereof which are useful as TEAD inhibitors. One of the embodiments of the present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof wherein A is pyridyl, tetrahydropyranyl, a 4-10 membered carbocyclic ring; L is -O-, -S-, -NH-, -C _1-7 alkyl-, -C _2-7 alkenyl-, -C _1-7 alkyl-O-, -O-C _1-7 alkyl- or -NH-C _1-7 alkyl-; R ₁ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, hydroxyl, cyano, -C(O)NR ₃₆ R ₃₇ , or an optionally substituted 5-6 membered heterocyclic ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; R ₂ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy or halogen; R ₃ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl or cyano, or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₄ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, cyano or C _1-7 alkylcarbonyl; R ₅ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, halogen, nitro, amino, hydroxyl, halogen C _1-7 alkyl, halogen C _1-7 alkoxy, or R ₄ and R ₅ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N; Z is –CH(NHR ₂₅ )-(CH ₂ ) ₂ -COOH or a group of formula wherein B is any one of the following groups provided that when B is ring (2), then L is -O- or -O-C _1-7 alkyl-, and R ₁ is C _1-7 alkoxy; when B is ring (3), then L is -O-; when B is ring (4), then L is -O- and R ₁ is C _1-7 alkoxy; when B is ring (20), (21), (23), (25) or (26), then L is -O- and R ₁ is C _1-7 alkoxy; when L is -C _1-7 alkyl-O-, then R ₁ is C _1-7 alkoxy or R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; when A is a 4-, 5-, 7-, 8-, 9- or 10-membered carbocyclic ring, then R ₁ is C _1-7 alkoxy; R ₆ and R ₉ are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, C _3-7 cyclo- alkyl C _1-7 alkyl, -C(O)-RX, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkoxycarbonyl C _1-7 alkyl, -SO ₂ C _1-7 alkyl, -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; RX is C _1-7 alkyl, C _3-7 cycloalkyl, C _1-7 alkoxy C _1-7 alkyl, C _1-7 alkyl-NR ₃₆ R ₃₇ , or an optionally substituted 4-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N; R ₇ , R _8, R _10, R ₁₂ , R ₁₃ , R ₁₄ , R ₁₅ , R ₁₆ , R ₁₇ , R ₁₈ , R ₁₉ , R ₂₀ , R ₂₁ , R ₂₂ and R ₂₆ are, independently, hydrogen, C _1-7 alkyl, C _3-7 cycloalkyl, hydroxyl, C _1-7 alkoxy or C _1-7 alkylcarbonyl; R ₁₁ is hydrogen, C _1-7 alkyl, halogen C _1-7 alkyl or C _1-7 alkylcarbonyl; R ₂₃ , R ₂₄ , R ₂₇ , R ₂₈ , R ₂₉ , R ₃₁ , R ₃₂ , R ₃₃ , R ₃₄ , R ₃₅ , R ₃₆ , R ₃₇ , R ₄₀ , R ₄₁ , R ₄₂ , R ₄₃ , R ₄₄ , and R ₄₅ are, independently, hydrogen, or C _1-7 alkyl; R ₂₅ is C _1-7 alkyl; R ₃₀ is C _1-7 alkyl, C _1-7 alkylcarbonyl or -SO ₂ C _1-7 alkyl; R ₃₈ is hydrogen, C _1-7 alkyl, C _1-7 alkylcarbonyl, C _1-7 alkoxy C _1-7 alkylcarbonyl or -C _1-7 alkyl-C(O)-NR ₂₃ R ₂₄ ; R ₃₉ is hydrogen, C _1-7 alkyl or hydroxyl; wherein optional substitution, in each occurrence, is 1-2 substituents independently selected from C _1-7 alkyl, halogen, halogen C _1-7 alkyl, C _1-7 alkoxy and oxo; with the proviso that compound of formula (I) is not N-[2-Methyl-3-(phenoxymethyl)phenyl]-5-oxo-2-pyrrolidinecarb oxamide; N-[5-[(3-Fluorophenoxy)methyl]-2-methoxyphenyl]-1-methyl-5-o xo-2- pyrrolidinecarboxamide; N-[3-[(4-Chlorophenyl)methyl]phenyl]-5-oxo-2-pyrrolidinecarb oxamide; N-[3-[(Cyclohexyloxy)methyl]phenyl]-1-methyl-5-oxo-2-pyrroli dine- carboxamide; N-[4-Methyl-3-[(4-methyl-2-pyridinyl)oxy]phenyl]-5-oxo-2-pyr rolidine- carboxamide; N-[3-(Cyclopentylamino)phenyl]-1-methyl-5-oxo-2-pyrrolidinec arboxamide; N-[3-[[(3-Methylcyclohexyl)oxy]methyl]phenyl]-6-oxo-3-piperi dine- carboxamide; 1-Ethyl-5-oxo-N-(3-phenoxyphenyl)-3-pyrrolidinecarboxamide; N-[5-[(3-Fluorophenoxy)methyl]-2-methoxyphenyl]-2-pyrrolidin ecarboxamide; 1-(1-Ethylpropyl)-N-[5-[(3-fluorophenoxy)methyl]-2-methoxyph enyl]-5-oxo-3- pyrrolidinecarboxamide; N-[3-[(4-Chlorophenyl)methyl]phenyl]-1,6-dihydro-6-oxo-3-pyr idine- carboxamide; 1,6-Dihydro-N-[4-methoxy-3-(phenylmethyl)phenyl]-6-oxo-3-pyr idine- carboxamide; 1,6-Dihydro-6-oxo-N-[3-[2-(2-pyridinyl)ethenyl]phenyl]-3- pyridinecarboxamide; N-[3-[(3-Fluorophenoxy)methyl]phenyl]-2,3-dihydro-2-oxo-1H-i midazole-4- carboxamide; 1-Methyl-N-[2-methyl-3-(phenoxymethyl)phenyl]-5-oxo-3-pyrrol idine- carboxamide; N-[3-[(1,3-Benzodioxol-5-yloxy)methyl]phenyl]-1-(2-methylpro pyl)-5-oxo-3- pyrrolidinecarboxamide; 1,6-Dihydro-N-[3-[[(3-methylcyclohexyl)oxy]methyl]phenyl]-6- oxo-3-pyridine- carboxamide; N-[3-[(Cyclohexyloxy)methyl]phenyl]-1-ethyl-5-oxo-3-pyrrolid inecarboxamide; 1-Methyl-N-[3-[[(3-methylcyclohexyl)oxy]methyl]phenyl]-5-oxo -3-pyrrolidine- carboxamide; 2,3-Dihydro-3-methyl-N-[3-[[(3-methylcyclohexyl)oxy]methyl]p henyl]-2-oxo- 1H-imidazole-4-carboxamide; 2,3-Dihydro-1,3-dimethyl-N-[3-[[(3-methylcyclohexyl)oxy]meth yl]phenyl]-2- oxo-1H-imidazole-4-carboxamide; 1-Ethyl-N-[4-methoxy-3-(4-pyridinylmethoxy)phenyl]-5-oxo-3-p yrrolidine- carboxamide; N-[4-Methoxy-3-(4-methoxyphenoxy)phenyl]-1-(2-methylpropyl)- 5-oxo-3- pyrrolidinecarboxamide or 6-Oxo-N-(3-phenoxyphenyl)-2-piperazinecarboxamide. It is to be understood that the left bond of variants of linker L is attached to the ring A of formula (I) and the right bond to the phenyl group. The wavy line in variants of group B denotes the site of attachment to carboxamide group. According to one embodiment, specifically provided is a compound according to formula (I) wherein A is phenyl, pyridyl or cyclohexyl. In a subgroup of the preceding embodiment, A is phenyl or cyclohexyl. In still another subgroup A is phenyl or pyridyl. In still another subgroup A is phenyl. In still another subgroup A is cyclohexyl. In still another subgroup A is pyridyl. According to yet one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₄₂ is hydrogen. According to one embodiment, specifically provided are compounds according to formula (Ia) or a pharmaceutically acceptable salt thereof wherein A, L, B, R ₁ , R _2, R _3, R ₄ , R ₅ , R ₃₃ and R ₄₂ are as defined above. According to yet one embodiment, specifically provided are compounds according to any of the above embodiments wherein B is ring (1a), (3), (4), (6), (8), (9), (10), (11), (12), (13), (16), (17) or (18). In a subgroup of the preceding embodiment, B is ring (1a), (4), (10), (11), (12), (13), (16) or (17). In still another subgroup B is ring (1a), (10), (11) or (12). In still another subgroup B is ring (1a) or (12). In still another subgroup B is ring (1a). In still another subgroup B is ring (12). In a subgroup of compounds wherein B is ring (1a) are compounds wherein R7 and R8 are hydrogen. In still another subgroup of the preceding embodiment are compounds wherein R6 is hydrogen, C _1-7 alkyl or C _3-7 cycloalkyl. According to another subgroup are compounds wherein R ₆ is -C(O)-R _X , wherein R _X is C _1-7 alkyl or an optionally substituted 4-6 membered ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N. Particular examples of such rings are pyrrolidine and azetidine rings optionally substituted by 1-2 substituents independently selected from C _1-7 alkyl and oxo. In a subgroup of compounds wherein B is ring (12) are compounds wherein R20 is hydrogen and R18 is C _1-7 alkyl or C _3-7 cycloalkyl. In still another subgroup of the preceding embodiment are compounds wherein R ₂₁ is hydrogen or C _1-7 alkyl. According to yet one embodiment, specifically provided are compounds according to any of the above embodiments wherein L is -O-, -S-, -NH-, -C _1-7 alkyl-, -C _2-7 alkenyl-, -C _1-7 alkyl-O-, or -O-C _1-7 alkyl-. In a subgroup of the preceding embodiment are compounds wherein L is -O-, -C _2-7 alkenyl-, -C _1-7 alkyl-O-, or -O-C _1-7 alkyl-. In a subgroup of the preceding embodiment are compounds wherein L is -O-, -C _2-7 alkenyl- or -O-C _1-7 alkyl-. In still another subgroup L is -O- or -C _2-7 alkenyl-. In still another subgroup L is -O-. A particular example of L being C _1-7 alkyl is -CH ₂ - group. A particular example of L being -C _2-7 alkenyl- is -CH=CH- group. A particular example of L being -C _1-7 alkyl-O- is -CH ₂ -O- group. A particular example of L being - O-C _1-7 alkyl- is –O-CH ₂ - group. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₁ is hydrogen, C _1-7 alkoxy or halogen. In a subgroup of the preceding embodiment are compounds wherein R ₁ is C _1-7 alkoxy or halogen. In a subgroup of the preceding embodiment are compounds wherein R ₁ is C _1-7 alkoxy, particularly a methoxy group. According to one embodiment, R ₁ is an optionally substituted 5-6 membered heterocyclic ring having 1-3 heteroatoms as ring atoms independently selected from O, S and N. Particular examples of such rings include oxadiazolyl and pyrazolyl rings optionally substituted by 1-2 C _1-7 alkyl or oxo substituents. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₂ is hydrogen, C _1-7 alkoxy or halogen. In a subgroup of the preceding embodiment are compounds wherein R ₂ is hydrogen or halogen. In a subgroup of the preceding embodiment are compounds wherein R ₂ is hydrogen. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₃ is hydrogen, halogen or C _1-7 alkoxy. In a subgroup are compounds wherein R ₃ is hydrogen or C _1-7 alkoxy. In a subgroup are compounds wherein R ₃ is hydrogen. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₁ and R ₃ together with the carbon atoms to which they are attached form an optionally substituted 5-6 membered ring having 0-3 heteroatoms as ring atoms independently selected from O, S and N. In a subgroup are compounds wherein R ₁ and R ₃ together with the carbon atoms to which they are attached form a 5-6 membered ring having 1-2 heteroatoms as ring atoms independently selected from O and N. In a subgroup are compounds wherein R ₁ and R ₃ together with the carbon atoms to which they are attached form a 5-6 membered ring having 1-2 heteroatoms wherein the heteroatom is O. Particular examples of such rings are furanyl, dihydrofuranyl, tetrahydrofuranyl, dioxanyl, dioxolanyl, oxazinyl, pyridinyl, 2,3- dihydro-1,4-dioxinyl, 2,3-dihydro-1,4-oxazinyl rings optionally substituted by 1-2 substituents independently selected from C _1-7 alkyl and oxo. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₁ and R ₃ together with the phenyl ring to which they are attached form an optionally substituted fused ring represented by any of the following groups: wherein the left wavy line denotes the site of attachment to the L group and the right wavy line denotes the site of attachment to the carboxamide group. The optional substitution may be 1-2 substituents independently selected from C _1-7 alkyl, halogen, halogen C _1-7 alkyl, C _1-7 alkoxy and oxo, in particular C _1-7 alkyl or oxo. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein R ₄ is hydrogen, halogen, C _1-7 alkyl, C _1-7 alkoxy, halogen C _1-7 alkyl or halogen C _1-7 alkoxy, and R ₅ is hydrogen, C _1-7 alkyl, C _1-7 alkoxy, cyano, amino or halogen. In a subgroup are compounds wherein R ₄ is halogen, C _1-7 alkyl, halogen C _1-7 alkyl or halogen C _1-7 alkoxy and R ₅ is hydrogen, C _1-7 alkyl, cyano or halogen. In a subgroup are compounds wherein R ₄ is halogen C _1-7 alkyl or halogen C _1-7 alkoxy and R ₅ is hydrogen or halogen. In a subgroup are compounds wherein R ₄ is halogen C _1-7 alkyl or halogen C _1-7 alkoxy and R ₅ is hydrogen. In another subgroup are compounds wherein both R ₄ and R ₅ are C _1-7 alkyl, for example methyl. In another subgroup are compounds wherein both R ₄ and R ₅ are halogen, for example fluoro. Particular examples of R ₄ being halogen C _1-7 alkyl is -CF ₃ and -CHF ₂ groups. A particular example of R ₄ being halogen C _1-7 alkoxy is -OCF ₃ group. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein ring A together with R ₄ and R ₅ represent any of the following groups: wherein X is halogen and the wavy line denotes the site of attachment to the L group. According to one embodiment, specifically provided is a compound according to any of the above embodiments wherein A together with R ₄ and R ₅ is group (1’), (2’), (3’), (4’), (7’), (8’), (10’), (11’) or (13’). In a subgroup are provided a compound according to any of the above embodiments wherein A together with R ₄ and R ₅ is group (1’), (4’), (7’), (8’), (10’) or (11’). According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein ring A together with R ₄ and R ₅ are represented by following groups: , wherein the wavy line denotes the site of attachment to the L group. According to one embodiment, specifically provided is a compound according to any of the above embodiments wherein A together with R ₄ and R ₅ is group (1’’), (2’’), (3’’), (4’’), (7’’), (11’’), (12’’), (13’’), (15’’), (17’’), (19’’) or (21’’). In a subgroup are provided a compound according to any of the above embodiments wherein A together with R ₄ and R ₅ is group (1’’), (2’’), (4’’), (7’’), (11’’), (12’’), (15’’) or (21’’). According to one embodiment, specifically provided is a compound according to any of the above embodiments wherein A is phenyl or pyridyl, L is -O-, R ₁ is C _1-7 alkoxy, R ₂ , R ₃ , R ₅ , R ₃₃ and R ₄₂ are hydrogen, Z is ring (1a) or (12) and R ₄ is halogen C _1-7 alkyl. According to one embodiment, specifically provided are compounds according to any of the above embodiments wherein Z can also be –CH(NHR ₂₅ )-(CH ₂ ) ₂ -COOH. According to one embodiment, specifically provided are compounds according to formula (Ib) or a pharmaceutically acceptable salt thereof wherein D is CH or N; R ₂ is H or halogen; R ₄ is H, halogen or cyano; R ₅ is halogen or halogen C _1-7 alkyl; B is ring (1a), (10) or (12); R ₁ is –OCH ₃ or halogen, or R ₁ and R ₃ together with the phenyl ring to which they are attached form a fused ring represented by any of the following groups: According to one embodiment, specifically provided are compounds according to formula (Ic) or a pharmaceutically acceptable salt thereof wherein L is -O- or –CH=CH-; R ₂ is H or halogen; R ₄ is H, C _1-7 alkyl or halogen; R ₅ is halogen, C _1-7 alkyl or halogen C _1-7 alkyl; B is ring (1a), (10) or (12); R ₁ is -OCH ₃ or halogen, or R ₁ and R ₃ together with the phenyl ring to which they are attached form a fused ring represented by any of the following groups: According to still one embodiment, the present invention provides a method for the treatment of a disease or condition wherein inhibition of TEAD is desired, such as cancer and chronic pain, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of formula (I) as defined in any of the above embodiments. The compounds of the invention can be prepared by a variety of synthetic routes analogously to the methods known in the literature using suitable starting materials. The compounds according to formula (I) can be prepared e.g. analogously or according to the following reaction Schemes. Some compounds included in the formula (I) can be obtained by converting the functional groups of the other compounds of formula (I) obtained in accordance with the following Schemes, by well known reaction steps such as oxidation, reduction, hydrolysis, acylation, alkylation, amidation, amination, sulfonation and others. It should be noted that any appropriate leaving groups, e.g. N- protecting groups, such as a t-butoxycarbonyl (t-BOC) group or a phenylsulfonyl group, can be used in well known manner during the syntheses in order to improve the selectivity of the reaction steps. Compounds of formula (I) can be prepared, for example, according to Scheme 1, wherein A, L, Z, R ₁ , R _2, R _3, R ₄ , R ₅ , R ₃₃ and R ₄₂ are as defined above. In the method of Scheme 1, the aniline compound of formula [1] is coupled with a carboxylic acid derivative of formula [2] in a suitable solvent, such as anhydrous acetonitrile or DMF, in the presence of a suitable coupling reagent such as a combination of N,N,N',N'- tetramethylchloroformamidinium hexafluorophosphate and 1-methyl-1H-imidazole, or hexafluorophosphate azabenzotriazole tetramethyl uranium (HATU) and N,N- diisopropylethylamine (DIPEA) to produce a compound of formula (I). Alternatively, compounds of formula (I), wherein R ₄₂ is H, can be prepared according to Scheme 2, wherein A, L, Z, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ and R ₃₃ are as defined above and X is a halogen, for example bromo. In the method of Scheme 2, the compound of formula [3] is coupled with a carboxamide compound of formula [4] in a suitable solvent, such as toluene, in the presence a base, such as cesium carbonate, and a suitable catalyst system such as a combination Pd ₂ (dba) and 4,5-Bis(diphenylphosphino)-9,9- dimethylxanthene (XantPhos), or copper iodide and N1,N2-dimethylcyclohexane-1,2- diamine, to produce a compound of formula (I).

Compounds of formula (I) wherein L is -O- can also be prepared, for example, according to Scheme 3, wherein A, Z, R ₁ , R _2, R _3, R ₄ and R ₅ are as defined above. In the method of Scheme 3, the compound of formula [3] is condensed with a compound of formula [4] in a suitable solvent, such as tetrahydrofuran, in the presence of Mitsunobu reagents, such as triphenylphosphine (TPP) and diethyl azodicarboxylate (DEAD), to produce a compound of formula (I). SCHEME 3. Intermediate compounds can be prepared according to the methods disclosed in the literature or as disclosed in the present disclosure. For example, intermediate compounds of formula [1a], wherein L is -O-, can be prepared according to Scheme 4, wherein A, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ and R33 are as defined above. In the method of Scheme 4, a compound of formula [7] is coupled with a compound of formula [8] in a suitable solvent such as dichloromethane, in the presence of a base such as pyridine and a catalyst such as diacetoxycopper to produce a compound of formula [8], which can be subsequently reduced, for example, by hydrogenation in the presence of suitable catalyst such as palladium-in-carbon to obtain the intermediate of formula [1a].

Intermediate compounds of formula [3a] wherein L is –O-, can be prepared, for example, according to Scheme 5, wherein A, R ₁ , R _2, R _3, R ₄ , R ₅ and R ₃₃ are as defined above and X is a halogen, for example bromo. In the method of Scheme 5, a compound of formula [9] is coupled with a compound of formula [10] in a suitable solvent such as dichloromethane, in the presence of a base such as pyridine and a catalyst such as diacetoxycopper to produce a compound of formula [3a], SCHEME 5. Intermediate compounds of formula [5] can be prepared, for example, according to Scheme 6, wherein Z, R _1, R ₂ and R ₃ are as defined above. In the method of Scheme 6, a compound of formula [11] is coupled with a compound of formula [12] in a suitable solvent such as DMF in the presence of a base such as N,N-diisopropylethylamine (DIPEA) and a coupling agent such as hexafluorophosphate azabenzotriazole tetramethyl uranium (HATU) to produce the intermediate of formula {5].

Alternatively, the compounds of formula (I) can be prepared as disclosed in the specific Examples of the present disclosure. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in art to which the subject matter herein belongs. As used herein, the following definitions are supplied in order to facilitate the understanding of the present invention. The term “subject”, as employed herein, refers to humans and animals. The term “halo” or “halogen”, as employed herein as such or as part of another group, refers to chlorine, bromine, fluorine or iodine. Preferred halogens are chlorine and fluorine. The term “C _1-7 alkyl”, as employed herein as such or as part of another group, refers to a straight or branched chain saturated hydrocarbon group having 1, 2, 3, 4, 5, 6 or 7 carbon atom(s). Representative examples of C _1-7 alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl and n-hexyl. One preferred embodiment of “C _1-7 alkyl” is C _1-3 alkyl. The term “ C _1-3 alkyl” refers to an embodiment of “C _1-7 alkyl” having 1, 2 or 3 carbon atoms. Examples of “C _1-3 alkyl” include, but are not limited to, methyl, ethyl, n-propyl and iso-propyl. One preferred “C _1-7 alkyl” is methyl group. The term “C _2-7 alkenyl”, as employed herein as such or as part of another group, refers to an aliphatic hydrocarbon group having 2, 3, 4, 5, 6 or 7 carbon atoms and containing one or several double bonds. Representative examples include, but are not limited to, ethenyl, propenyl and hexenyl. One preferred embodiment of “C _2-7 alkenyl” is C _2-4 alkenyl. The term “ C _2-4 alkenyl” refers to a embodiment of “C _2-7 alkenyl” having 2, 3 or 4 carbon atoms. Representative examples include, but are not limited to, ethenyl, propenyl and butenyl. One preferred “C _2-7 alkenyl” is -CH=CH- group. The term “C _3-7 cycloalkyl”, as employed herein as such or as part of another group, refers to a saturated cyclic hydrocarbon group containing 3, 4, 5, 6 or 7 carbon atoms. Representative examples of cycloalkyl include, but are not limited to, cyclo- propyl, cyclobutyl, cyclopentyl and cyclohexyl. One preferred “C _3-7 cycloalkyl” is cyclopropyl group. The term “hydroxy”, as employed herein as such or as part of another group, refers to an –OH group. The term “cyano”, as employed herein as such or as part of another group, refers to a -CN group. The term “carboxy”, as employed herein as such or as part of another group, refers to -COOH group. The term “carbonyl”, as employed herein as such or as part of another group, refers to a carbon atom double-bonded to an oxygen atom (C=O). The term “oxo”, as employed herein as such or as part of another group, refers to oxygen atom linked to another atom by a double bond (=O). The term “C _1-7 alkoxy”, as employed herein as such or as part of another group, refers to C _1-7 alkyl, as defined herein, appended to the parent molecular moiety through an oxygen atom. Representative examples of C _1-7 alkoxy include, but are not limited to methoxy, ethoxy, propoxy, butoxy, isobutoxy, sec-butoxy and tert-butoxy. One preferred embodiment of “C _1-7 alkoxy” is C _1-3 alkoxy. The term “C _1-3 alkoxy” refers to an embodiment of “C _1-7 alkoxy” having 1, 2 or 3 carbon atoms. Representative examples of C _1-3 alkoxy include, but are not limited to methoxy, ethoxy, propoxy. One preferred “C _1-7 alkoxy” group is methoxy. The term “hydroxy C _1-7 alkyl”, as employed herein, refers to at least one hydroxy group, as defined herein, appended to the parent molecular moiety through a C _1-7 alkyl group, as defined herein. Representative examples of hydroxy C _1-7 alkyl include, but are not limited to, hydroxymethyl, 2,2-dihydroxyethyl, 1-hydroxyethyl, 3-hydroxypropyl, 1-hydroxypropyl, 1-methyl-1-hydroxyethyl and 1-methyl-1-hydroxypropyl. The term “halogen C _1-7 alkyl”, as employed herein, refers to at least one halogen, as defined herein, appended to the parent molecular moiety through a C _1-7 alkyl group, as defined herein. Representative examples of halogen C _1-7 alkyl include, but are not limited to, fluoromethyl, difluoromethyl, trifluoromethyl, 2-chloroethyl and 3-bromo- propyl. Preferred “halogen C _1-7 alkyl” groups are trifluoromethyl and difluoromethyl. The term “halogen C _1-7 alkoxy”, as employed herein, refers to at least one halogen, as defined herein, appended to the parent molecular moiety through a C _1-7 alkoxy group, as defined herein. The term “C _1-7 alkoxy C _1-7 alkyl”, as employed herein as such or as part of another group, refers to at least one C _1-7 alkoxy group, as defined herein, appended to the parent molecular moiety through a C _1-7 alkyl group, as defined herein. The term “4-10 membered carbocyclic ring”, as employed herein, refers to a saturated, partially saturated or aromatic ring with 4 to 10 ring atoms consisting of carbon atoms only. One embodiment of a "4-10 membered carbocyclic ring" is a “5-6 membered carbocyclic ring” which refers to a saturated, partially saturated or aromatic ring with 5 to 6 ring atoms consisting of carbon atoms only. Representative examples of a 4-10 membered carbocyclic ring include, but are not limited to, phenyl, cyclohexyl, cyclohexenyl, cyclopentyl, cyclopentenyl and cyclobutyl rings. The term "substituted" as used herein in connection with various residues refers to, if not otherwise defined, to halogen substituents, such as fluorine, chlorine, bromine, iodine, or C _1-7 alkyl, C _3-7 cycloalkyl, hydroxy, amino, nitro, cyano, thiol C _1-7 alkyl, methylsulfonyl, C _1-7 alkoxy, halo C _1-7 alkyl, hydroxy C _1-7 alkyl or amino C _1-7 alkyl substituents. Preferred are halogen, C _1-7 alkyl, hydroxy, amino, halo C _1-7 alkyl, C _1-7 alkoxy and methylsulfonyl substituents. In one group of preferred substituents are 1-2 substituents selected from C _1-7 alkyl or halogen substituents, particularly C _1-3 alkyl or halogen substituents, particularly methyl, ethyl, chloro, fluoro or bromo substituents. The "substituted" groups may contain 1 to 3, preferably 1 or 2, of the above mentioned substituents, if not otherwise defined. Optically active enantiomers or diastereomers of compounds of formula (I) can be prepared e.g. by resolution of the racemic end product by known methods or by using suitable optically active starting materials. Similarly, racemic compounds of formula (I) can be prepared by using racemic starting materials. Resolution of racemic compounds of formula (I) or a racemic starting material thereof can be carried out, for example, by converting the racemic compound into its diastereromeric salt mixture by reaction with an optically active acid and subsequent separation of the diastereomers by crystallization. Representative examples of said optically active acids include, but are not limited to, D-tartaric acid and dibenzoyl-D-tartaric acid. Alternatively, preparative chiral chromatography may be used for resolution of the racemic mixture. Pharmaceutically acceptable salts are well known in the field of pharmaceuticals. Non-limiting examples of suitable salts include metal salts, ammonium salts, salts with an organic base, salts with an inorganic acid, salts with organic acid, and salts with basic or acidic amino acid. Non-limiting examples of metal salts include alkali metal salts such as sodium salt and potassium salt; alkaline earth metal salts such as calcium salt, and magnesium salt. Non-limiting examples of salts with inorganic or organic acids include chlorides, bromides, sulfates, nitrates, phosphates, sulfonates, methane sulfonates, formates, tartrates, maleates, citrates, benzoates, salicylates, ascorbates, acetates, oxalates, fumarates, hemifumarates, and succinates. Pharmaceutically acceptable esters, when applicable, may be prepared by known methods using pharmaceutically acceptable acids that are conventional in the field of pharmaceuticals and that retain the pharmacological properties of the free form. Non-limiting examples of these esters include esters of aliphatic or aromatic alcohols, e.g. methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl esters. Phosphate esters and carbonate esters, are also within the scope of the invention. The definition of formula (I) above is inclusive of all the possible isotopes and isomers, such as stereoisomers, of the compounds, including geometric isomers, for example Z and E isomers (cis and trans isomers), and optical isomers, e.g. diastereomers and enantiomers, and prodrug esters, e.g. phosphate esters and carbonate esters. It will be appreciated by those skilled in the art that the present compounds may contain at least one chiral center. Accordingly, the compounds may exist in optically active or racemic forms. It is to be understood that the formula (I) includes any racemic or optically active form, or mixtures thereof. In one embodiment, the compounds are the pure (R)-isomers. In another embodiment, the compounds are the pure (S)-isomers. In another embodiment, the compounds are a mixture of the (R) and the (S) isomers. In another embodiment, the compounds are a racemic mixture comprising an equal amount of the (R) and the (S) isomers. The compounds may contain two chiral centers. In such case, according to one embodiment, the compounds are a mixture of diasteromers. According to another embodiment, the compounds of the invention are a mixture of enantiomers. According to still another embodiment, the compounds are pure enantiomers. The individual isomers may be obtained using the corresponding isomeric forms of the starting material or they may be separated after the preparation of the end compound according to conventional separation methods. For the separation of optical isomers, e.g. enantiomers or diastereomers, from the mixture thereof the conventional resolution methods, e.g. fractional crystallisation, may be used. The present compounds may also exist as tautomers or equilibrium mixtures thereof wherein a proton of a compound shifts from one atom to another. Examples of tautomerism include, but are not limited to, amido-imido, keto-enol, phenol-keto, oxime-nitroso, nitro-aci, imine-enamine, annular tautomerism of heterocyclic rings such as pyrozole ring, and the like. Tautomeric forms are intended to be encompassed by compounds of formula (I), even though only one tautomeric form may be depicted. Examples of preferred compounds of one group of formula (I) include N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 1); 1-Acetyl-N-(5-(3-fluorophenoxy)-2-methoxyphenyl)-5-oxopyrrol idine-2- carboxamide (Compound 2); 1-Acetyl-N-(5-((3-fluorophenoxy)methyl)-2-methoxyphenyl)-5-o xopyrrolidine- 2-carboxamide (Compound 3); N-(5-((3-Fluorophenoxy)methyl)-2,4-dimethoxyphenyl)-5-oxopyr rolidine-2- carboxamide (Compound 4); 1-(2-Fluoroethyl)-N-(5-((3-fluorophenoxy)methyl)-2-methoxyph enyl)azetidine- 3-carboxamide (Compound 5); rac-(trans)-N-(5-((3-Fluorophenoxy)methyl)-2-methoxyphenyl)- 3-methyl-5- oxopyrrolidine-2-carboxamide (Compound 6); 4-Oxo-N-(3-(3-(trifluoromethyl)phenoxy)phenyl)azetidine-2-ca rboxamide (Compound 7); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-4-oxoazet idine-2- carboxamide (Compound 8); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-2-(5-oxop yrrolidin-2- yl)acetamide (Compound 9); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 10); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxopyrro- lidine-2-carboxamide (Compound 11); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)tetrahydro thiophene-3- carboxamide 1,1-dioxide (Compound 12); N-(5-((3-Fluorophenoxy)methyl)-2-methoxyphenyl)-2-methylisot hiazolidine-3- carboxamide 1,1-dioxide (Compound 13); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-2-methyl- 5-oxopyrrolidi- ne-2-carboxamide (Compound 14); N-(5-(3-Fluorophenoxy)-2-methoxyphenyl)-2-methyl-5-oxopyrrol idine-2- carboxamide (Compound 15); 5-Oxo-N-(3-(3-(trifluoromethyl)phenoxy)phenyl) pyrrolidine-2-carboxamide (Compound 16); N-(5-((3-Fluorophenoxy)methyl)benzofuran-7-yl)-5-oxopyrrolid ine-2- carboxamide (Compound 17); N-(5-(3-Fluorophenoxy)-2-methoxyphenyl)-5-oxotetrahydropyrro lo[2,1-b]- thiazole-7a(5H)-carboxamide (Compound 18); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-5-oxotetr ahydro- pyrrolo[2,1-b]thiazole-7a(5H)-carboxamide (Compound 19); rac-(cis)-N-(5-((3-Fluorophenoxy)methyl)-2-methoxyphenyl)-3- methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 20); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 5-oxopyrroli- dine-2-carboxamide (Compound 21); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 1-methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 22); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 5-oxopyrroli- dine-2-carboxamide, enantiomer 1 (Compound 23); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 5-oxopyrrolidi- ne-2-carboxamide, enantiomer 1 (Compound 24); (R)-N-(5-(3-Fluorophenoxy)-2-methoxyphenyl)-5-oxopyrrolidine -2- carboxamide (Compound 25); N-(5-((3-Fluorophenoxy)methyl)-2-methoxyphenyl)-3-methyl-2-o xopyrrolidine- 3-carboxamide (Compound 26); N-(6-((3-Fluorophenoxy)methyl)benzo[d][1,3]dioxol-4-yl)-5-ox opyrrolidine-2- carboxamide (Compound 27); 1-Methyl-5-oxo-N-(5-(3-(trifluoromethyl)phenoxy)benzofuran-7 -yl)pyrrolidine- 2-carboxamide (Compound 28); 1-Acetyl-N-(2-methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)- 5-oxo- pyrrolidine-2-carboxamide (Compound 29); 1-Acetyl-N-(2-methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)- 5-oxo- pyrrolidine-2-carboxamide, enantiomer 2 (Compound 30); N-(5-((3-Fluorophenoxy)methyl)-2,3-dihydrobenzofuran-7-yl)-5 -oxopyrrolidine- 2-carboxamide (Compound 31); N-(5-((3-Fluorophenoxy)methyl)-2,3-dihydrobenzofuran-7-yl)-1 -methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 32); 5-Oxo-N-(6-(3-(trifluoromethyl)phenoxy)benzo[d][1,3]dioxol-4 -yl)pyrrolidine- 2-carboxamide (Compound 33); 1-Methyl-5-oxo-N-(6-(3-(trifluoromethyl)phenoxy)benzo[d][1,3 ]dioxol-4-yl)- pyrrolidine-2-carboxamide (Compound 34); N-(3-Fluoro-5-((3-fluorophenoxy)methyl)-2-methoxyphenyl)-1-m ethyl-5-oxo- pyrrolidine-2-carboxamide (Compound 35); N-(3-Fluoro-5-((3-fluorophenoxy)methyl)-2-methoxyphenyl)-5-o xopyrrolidine- 2-carboxamide (Compound 36); 1-Ethyl-N-(2-methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-5 -oxopyrrolidine- 2-carboxamide (Compound 37); 1-(Cyclopropanecarbonyl)-N-(2-methoxy-5-(3-(trifluoromethyl) phenoxy)- phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 38); 1-Acetyl-N-(4-fluoro-2-methoxy-5-(3-(trifluoromethyl)phenoxy )phenyl)-5- oxopyrrolidine-2-carboxamide (Compound 39); 1-Acetyl-N-(2-fluoro-5-(3-(trifluoromethyl)phenoxy)phenyl)-5 -oxopyrrolidine- 2-carboxamide (Compound 40); N-(2-Fluoro-5-(3-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 41); N-(5-(2,4-Difluorophenoxy)-2-methoxyphenyl)-5-oxopyrrolidine -2-carboxamide (Compound 42); N-(5-(2,4-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 43); 1-Acetyl-N-(5-(2,4-difluorophenoxy)-2-methoxyphenyl)-5-oxopy rrolidine-2- carboxamide (Compound 44); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 45); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 46); 1-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 5-oxo- pyrrolidine-2-carboxamide (Compound 47); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxopyrrolidi- ne-2-carboxamide (Compound 48); N-(2-Methoxy-5-((3-(trifluoromethyl)phenoxy)methyl)phenyl)-5 - oxopyrrolidine-2-carboxamide (Compound 49); 1-Acetyl-N-(2-methoxy-5-((3-(trifluoromethyl)phenoxy)methyl) phenyl)-5- oxopyrrolidine-2-carboxamide (Compound 50); 1-Acetyl-N-(2-methoxy-5-((3-(trifluoromethyl)benzyl)oxy)phen yl)-5-oxo- pyrrolidine-2-carboxamide (Compound 51); N-(2-Methoxy-5-((3-(trifluoromethyl)benzyl)oxy)phenyl)-5-oxo pyrrolidine-2- carboxamide (Compound 52); N-(2-Methoxy-5-((3-(trifluoromethyl)benzyl)oxy)phenyl)-1-met hyl-5-oxo- pyrrolidine-2-carboxamide (Compound 53); N-(7-(3-(Trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][1,4]di oxin-5-yl)- isothiazolidine-3-carboxamide 1,1-dioxide (Compound 54); 5-Oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][ 1,4]dioxin-5- yl)pyrrolidine-2-carboxamide (Compound 55); 1-Acetyl-5-oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)pyrrolidine-2-carboxamide (Compound 56); N-(7-((3-Fluorophenoxy)methyl)-2,3-dihydrobenzo[b][1,4]dioxi n-5-yl)-5- oxopyrrolidine-2-carboxamide (Compound 57); N-(7-((3-Fluorophenoxy)methyl)-2,3-dihydrobenzo[b][1,4]dioxi n-5-yl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 58); N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-5-oxopyrrolidine -2-carboxamide (Compound 59); N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 60); N-(8-Methyl-7-(3-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[ b][1,4]dioxin-5- yl)-5-oxopyrrolidine-2-carboxamide (Compound 61); N-(2-Methoxy-5-((6-(trifluoromethyl)pyridin-3-yl)oxy)phenyl) -5- oxopyrrolidine-2-carboxamide (Compound 62); N-(2-Methoxy-5-((6-(trifluoromethyl)pyridin-3-yl)oxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 63); (E)-N-(2-Methoxy-5-(2-(tetrahydro-2H-pyran-4-yl)vinyl)phenyl )-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 64); (E)-N-(2-Methoxy-5-(2-(tetrahydro-2H-pyran-4-yl)vinyl)phenyl )-5-oxo- pyrrolidine-2-carboxamide (Compound 65); 5-Oxo-N-(7-(4-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][ 1,4]dioxin-5- yl)pyrrolidine-2-carboxamide (Compound 66); 1-Methyl-5-oxo-N-(7-(4-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)pyrrolidine-2-carboxamide (Compound 67); 1-Ethyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5 -oxopyrrolidine- 2-carboxamide (Compound 68); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-met hyl-5-oxo- pyrrolidine-2-carboxamide (Compound 69); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-met hyl-5-oxo- pyrrolidine-2-carboxamide (Compound 70); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-2-methyl- 1,2-thiazeti- dine-3-carboxamide 1,1-dioxide (Compound 71); N-(2-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-2-methyl- 1,2-thiaze- tidine-3-carboxamide 1,1-dioxide (Compound 72); N-(4-Fluoro-5-((3-fluorophenoxy)methyl)-2-methoxyphenyl)-5-o xopyrrolidine- 2-carboxamide (Compound 73); N-(2-Methoxy-5-((4-(trifluoromethyl)phenyl)amino)phenyl)-1-m ethyl-5-oxo- pyrrolidine-2-carboxamide (Compound 74); N-(2-Fluoro-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 75); N-(2-Fluoro-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrro lidine-2- carboxamide (Compound 76); 1-Acetyl-N-(5-(3,5-difluorophenoxy)-2-methoxyphenyl)-5-oxopy rrolidine-2- carboxamide (Compound 77); N-(5-(3,5-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 78); N-(5-(2,5-Difluorophenoxy)-2-methoxyphenyl)-5-oxopyrrolidine -2-carboxamide (Compound 79); 3-Oxo-N-(7-(4-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][ 1,4]dioxin-5- yl)tetrahydro-1H-pyrrolizine-7a(5H)-carboxamide (Compound 80); 1-Isopropyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)pheny l)-5-oxo- pyrrolidine-2-carboxamide (Compound 81); N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-1-isopropyl-5-ox opyrrolidine-2- carboxamide (Compound 82); N-(2-(1,3,4-Oxadiazol-2-yl)-5-(4-(trifluoromethyl)phenoxy)ph enyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 83); N-(2-(1,3,4-Oxadiazol-2-yl)-5-(3-(trifluoromethyl)phenoxy)ph enyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 84); N-(5-(3,4-Difluorophenoxy)-2-(1-methyl-1H-pyrazol-3-yl)pheny l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 85); N-(5-(3,4-Difluorophenoxy)-2-(1-methyl-1H-pyrazol-5-yl)pheny l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 86); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-methyl- 2-oxo- oxazolidine-4-carboxamide (Compound 87); N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-3-methyl-2-oxoox azolidine-4- carboxamide (Compound 88); N-(5-((3,4-Difluorophenoxy)methyl)-2-methoxyphenyl)-3-methyl -2-oxo- oxazolidine-4-carboxamide (Compound 89); N-(5-((3-Fluorophenoxy)methyl)-2-methoxyphenyl)-3-methyl-2-o xo- oxazolidine-4-carboxamide (Compound 90); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-thioxo- pyrrolidine-2-carboxamide (Compound 91); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-thioxop yrrolidine-2- carboxamide (Compound 92); (R)-N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (Compound 93); (S)-N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (Compound 94); N-(5-((3,4-Difluorophenoxy)methyl)-2-methoxyphenyl)-1-methyl -5-oxo- pyrrolidine-2-carboxamide (Compound 95); N-(5-(Bicyclo[2.2.1]heptan-2-yloxy)-2-methoxyphenyl)-1-methy l-5-oxo- pyrrolidine-2-carboxamide (Compound 96); (R)-N-(7-(3,4-Difluorophenoxy)-2,3-dihydrobenzo[b][1,4]dioxi n-5-yl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 97); (S)-N-(7-(3,4-Difluorophenoxy)-2,3-dihydrobenzo[b][1,4]dioxi n-5-yl)-1-methyl- 5-oxopyrrolidine-2-carboxamide (Compound 98); (R)-1-Methyl-5-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dih ydrobenzofuran- 7-yl)pyrrolidine-2-carboxamide (Compound 99); (S)-N-(5-(3,4-Difluorophenoxy)-2,3-dihydrobenzofuran-7-yl)-1 -methyl-5- oxopyrrolidine-2-carboxamide (Compound 100); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-met hyl-2- oxooxazolidine-4-carboxamide (Compound 101); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-met hyl-2- oxooxazolidine-4-carboxamide (Compound 102); (R)-N-(2-Methoxy-5-(((trans)-4-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 103); N-(5-((4,4-Difluorocyclohexyl)oxy)-2-methoxyphenyl)-3-methyl -2-oxo- oxazolidine-4-carboxamide (Compound 104); (S)-N-(2-Methoxy-5-(((trans)-4-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 105); 1-Methyl-5-oxo-N-(3-oxo-7-(3-(trifluoromethyl)phenoxy)-3,4-d ihydro-2H- benzo[b][1,4]oxazin-5-yl)pyrrolidine-2-carboxamide (Compound 106); (S)-1-Methyl-5-oxo-N-(5-(((cis)-4-(trifluoromethyl)cyclohexy l)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 107); (R)-1-Methyl-5-oxo-N-(5-(((cis)-4-(trifluoromethyl)cyclohexy l)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 108); 1-Cyclopropyl-5-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-di hydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 109); 1-Cyclopropyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phe nyl)-5-oxo- pyrrolidine-2-carboxamide (Compound 110); 1-Cyclopropyl-N-(5-(3,4-difluorophenoxy)-2-methoxyphenyl)-5- oxopyrrolidine- 2-carboxamide (Compound 111); N-(2-Methoxy-5-((5-(trifluoromethoxy)pyridin-2-yl)oxy)phenyl )-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 112); N-(7-(((4,4-Difluorocyclohexyl)oxy)methyl)-2,3-dihydrobenzo[ b][1,4]dioxin-5- yl)-1-methyl-5-oxopyrrolidine-2-carboxamide (Compound 113); 1-Cyclopropyl-5-oxo-N-(7-(4-(trifluoromethyl)phenoxy)-2,3-di hydro- benzo[b][1,4]dioxin-5-yl)pyrrolidine-2-carboxamide (Compound 114); N-(2-Methoxy-5-((5-(trifluoromethoxy)pyridin-2-yl)oxy)phenyl )-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 115); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)tetrahydro thiophene-3- carboxamide 1,1-dioxide (Compound 116); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-methyl- 2-oxo- imidazolidine-4-carboxamide (Compound 117); N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 118); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-6-oxo piperidine-3- carboxamide (Compound 119); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-6-oxo piperidine-3- carboxamide (Compound 120); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-methyl- 6-oxo- piperidine-3-carboxamide (Compound 121); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-6-oxo-1,6 -dihydro- pyridine-3-carboxamide (Compound 122); N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -3,4-dimethyl-2- oxoimidazolidine-4-carboxamide (Compound 123); (R)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 124); (S)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 125); (R)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 126); 3-Ethyl-N-(2-methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy )phenyl)-2-oxo- imidazolidine-4-carboxamide (Compound 127); (R)-1-Cyclopropyl-N-(2-methoxy-5-((5-(trifluoromethyl)pyridi n-2-yl)oxy)- phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 128); (S)-1-Cyclopropyl-N-(2-methoxy-5-((5-(trifluoromethyl)pyridi n-2-yl)oxy)- phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 129); (S)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 130); 3-Cyclopropyl-N-(2-methoxy-5-((5-(trifluoromethyl)pyridin-2- yl)oxy)phenyl)- 2-oxoimidazolidine-4-carboxamide (Compound 131); 1-(Cyclopropylmethyl)-N-(2-methoxy-5-((5-(trifluoromethyl)py ridin-2-yl)oxy)- phenyl)-5-oxopyrrolidine-2-carboxamide, enantiomer 1 (Compound 132); 1-(Cyclopropylmethyl)-N-(2-methoxy-5-((5-(trifluoromethyl)py ridin-2-yl)oxy)- phenyl)-5-oxopyrrolidine-2-carboxamide, enantiomer 2 (Compound 133); (R)-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,2-d imethyl-5- oxopyrrolidine-2-carboxamide (Compound 134); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,2-d imethyl-5-oxo- pyrrolidine-2-carboxamide (Compound 135); 1-(2-Amino-2-oxoethyl)-N-(2-methoxy-5-(4-(trifluoromethyl)ph enoxy)phenyl)- 5-oxopyrrolidine-2-carboxamide (Compound 136); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(1-meth yl-1H-pyrazol- 4-yl)-5-oxopyrrolidine-2-carboxamide (Compound 137); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo-1-( tetrahydrofuran- 3-yl)pyrrolidine-2-carboxamide (Compound 138); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,3-dimet hyl-2-oxo- imidazolidine-4-carboxamide (Compound 139); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-met hyl-2-oxo- imidazolidine-4-carboxamide (Compound 140); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-met hyl-2- oxoimidazolidine-4-carboxamide (Compound 141); 3-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 1-methyl-2- oxoimidazolidine-4-carboxamide (Compound 142); (2S)-4-Methoxy-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)ph enyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 143); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-2-oxoimid azolidine-4- carboxamide (Compound 144); N-(2-Methoxy-4-(4-(trifluoromethyl)phenoxy)phenyl)-1-(2-(met hylamino)-2- oxoethyl)-5-oxopyrrolidine-2-carboxamide (Compound 145); 1-(2-(Dimethylamino)-2-oxoethyl)-N-(2-methoxy-4-(4-(trifluor omethyl)- phenoxy)phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 146); 1-(Cyclopropylmethyl)-N-(2-methoxy-5-(4-(trifluoromethyl)phe noxy)phenyl)-5- oxopyrrolidine-2-carboxamide, enantiomer 1 (Compound 147); 1-(Cyclopropylmethyl)-N-(2-methoxy-5-(4-(trifluoromethyl)phe noxy)phenyl)-5- oxopyrrolidine-2-carboxamide, enantiomer 2 (Compound 148); N-(5-(4-(Difluoromethyl)phenoxy)-2-methoxyphenyl)-3-methyl-2 -oxoimidazoli- dine-4-carboxamide (Compound 149); (S)-1-Methyl-5-oxo-N-(5-(((trans)-4-(trifluoromethyl)cyclohe xyl)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 150); (R)-1-Methyl-5-oxo-N-(5-(((trans)-4-(trifluoromethyl)cyclohe xyl)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 151); N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)ox y)phenyl)-3- methyl-2-oxooxazolidine-4-carboxamide (Compound 152); N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)ox y)phenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 153); (R)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)-oxy)phenyl)-3- methyl-2-oxooxazolidine-4-carboxamide (Compound 154); (R)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)phenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 155); (S)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)phenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 156); (S)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)phenyl)-3- methyl-2-oxooxazolidine-4-carboxamide (Compound 157); N-(5-(2-Chloro-4-(trifluoromethyl)phenoxy)-4-fluoro-2-methox yphenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 158); 3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2 ,3-dihydrobenzo- furan-7-yl)imidazolidine-4-carboxamide (Compound 159); 2-Oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2,3-dihydr obenzofuran-7-yl)- piperidine-4-carboxamide (Compound 160); 6-Oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2,3-dihydr obenzofuran-7- yl)piperidine-3-carboxamide (Compound 161); (R)-1-Methyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)-2,3-dihydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 162); (S)-1-Methyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)-2,3-dihydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 163); 3-Cyclopropyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)o xy)-2,3-dihydro- benzofuran-7-yl)imidazolidine-4-carboxamide (Compound 164); (S)-1-Cyclopropyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2- yl)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 165); (R)-1-Cyclopropyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2- yl)oxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 166); 3-Ethyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2, 3-dihydrobenzo- furan-7-yl)imidazolidine-4-carboxamide (Compound 167); (S)-3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)-2,3-dihydro- benzofuran-7-yl)imidazolidine-4-carboxamide (Compound 168); (R)-3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)-2,3-dihydro- benzofuran-7-yl)imidazolidine-4-carboxamide (Compound 169); (R)-1-Ethyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy )-2,3-dihydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 170); (S)-1-Ethyl-5-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy )-2,3-dihydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 171); (2R)-1-Methyl-N-(2-methyl-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)-2,3-di- hydrobenzofuran-7-yl)-5-oxopyrrolidine-2-carboxamide, enantiomer 1 (Compound 172); (2R)-1-Methyl-N-(2-methyl-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)-2,3-di- hydrobenzofuran-7-yl)-5-oxopyrrolidine-2-carboxamide, enantiomer 2 (Compound 173); (S)-1-Methyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)ox y)chroman-8- yl)pyrrolidine-2-carboxamide (Compound 174); (R)-1-Methyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)ox y)chroman-8- yl)pyrrolidine-2-carboxamide (Compound 175); 3-Methyl-2-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)ch roman-8-yl)- imidazolidine-4-carboxamide (Compound 176); 1-Methyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)ch roman-8-yl)- pyrrolidine-2-carboxamide (Compound 177); 3-Methyl-2-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)be nzo[d]- [1,3]dioxol-4-yl)imidazolidine-4-carboxamide (Compound 178); 1-Cyclopropyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)o xy)benzo[d]- [1,3]dioxol-4-yl)pyrrolidine-2-carboxamide (Compound 179); (S)-3-Methyl-2-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)ox y)benzo- [d][1,3]dioxol-4-yl)imidazolidine-4-carboxamide (Compound 180); (R)-3-Methyl-2-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)ox y)benzo- [d][1,3]dioxol-4-yl)imidazolidine-4-carboxamide (Compound 181); 3-Methyl-2-oxo-N-(7-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2 ,3-dihydrobenzo- [b][1,4]dioxin-5-yl)imidazolidine-4-carboxamide (Compound 182); 3-Methyl-2-oxo-N-(7-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2 ,3-dihydrobenzo- [b][1,4]dioxin-5-yl)imidazolidine-4-carboxamide, enantiomer 1 (Compound 183); 3-Methyl-2-oxo-N-(7-((5-(trifluoromethyl)pyridin-2-yl)oxy)-2 ,3-dihydrobenzo- [b][1,4]dioxin-5-yl)imidazolidine-4-carboxamide, enantiomer 2 (Compound 184); 1-Methyl-5-oxo-N-(5-(4-(trifluoromethyl)phenoxy)benzofuran-7 -yl)pyrrolidine- 2-carboxamide (Compound 185); 3-Methyl-2-oxo-N-(6-(4-(trifluoromethyl)phenoxy)benzo[d][1,3 ]dioxol-4-yl)- imidazolidine-4-carboxamide (Compound 186); 2-Oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dihydrobenzofura n-7-yl)- piperidine-4-carboxamide (Compound 187); 1-(2-(Methylamino)-2-oxoethyl)-5-oxo-N-(5-(4-(trifluoromethy l)phenoxy)-2,3- dihydrobenzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 188); 1-(2-Amino-2-oxoethyl)-5-oxo-N-(5-(4-(trifluoromethyl)phenox y)-2,3-dihydro- benzofuran-7-yl)pyrrolidine-2-carboxamide (Compound 189); N-(5-((4,4-Difluorocyclohexyl)oxy)-2,3-dihydrobenzofuran-7-y l)-6-oxo- piperidine-3-carboxamide (Compound 190); N-(7-((4,4-Difluorocyclohexyl)oxy)-2,3-dihydrobenzo[b][1,4]d ioxin-5-yl)-6- oxopiperidine-3-carboxamide (Compound 191); 3-Methyl-2-oxo-N-(7-(4-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)imidazolidine-4-carboxamide (Compound 192); 3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-1 H-indazol-7-yl)- imidazolidine-4-carboxamide (Compound 193); 1-Methyl-N-(1-methyl-5-((5-(trifluoromethyl)pyridin-4-yl)oxy )-1H-indazol-7- yl)-5-oxopyrrolidine-2-carboxamide (Compound 194); (S)-N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 195); (R)-N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 196); N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 3-methyl-2- oxooxazolidine-4-carboxamide (Compound 197); (R)-N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 198); (S)-N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 199); N-(2-Methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 200); N-(2-Methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 201); N-(5-((5-Fluoropyridin-2-yl)oxy)-2-methoxyphenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 202); N-(5-((5-Chloropyridin-2-yl)oxy)-2-methoxyphenyl)-1-methyl-5 -oxo- pyrrolidine-2-carboxamide (Compound 203); N-(5-(2-Fluoro-4-nitrophenoxy)-2-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (Compound 204); N-(5-(((4,4-Difluorocyclohexyl)oxy)methyl)-2-methoxyphenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 205); N-(5-((4,4-Difluorocyclohexyl)methoxy)-2-methoxyphenyl)-1-me thyl-5- oxopyrrolidine-2-carboxamide (Compound 206); (2S)-N-(5-((4,4-Difluorocycloheptyl)oxy)-2-methoxyphenyl)-1- methyl-5- oxopyrrolidine-2-carboxamide (Compound 207); (R)-N-(2-Methoxy-5-((4-(trifluoromethyl)cyclohexyl)oxy)pheny l)-3-methyl-2- oxooxazolidine-4-carboxamide (Compound 208); (R)-N-(2-Methoxy-5-(((cis)-4-(trifluoromethyl)cyclohexyl)oxy )phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 209); (S)-N-(2-Methoxy-5-(((cis)-4-(trifluoromethyl)cyclohexyl)oxy )phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 210); N-(5-((5-(Difluoromethyl)pyridin-2-yl)oxy)-2-methoxyphenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 211); N-(5-((5-(Difluoromethyl)pyridin-2-yl)oxy)-2-methoxyphenyl)- 3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 212); N-(5-(4-(Difluoromethyl)phenoxy)-2,3-dihydrobenzofuran-7-yl) -3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 213); (S)-N-(5-(4-(Difluoromethyl)phenoxy)-2,3-dihydrobenzofuran-7 -yl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 214); (R)-N-(5-(4-(Difluoromethyl)phenoxy)-2,3-dihydrobenzofuran-7 -yl)-1-methyl- 5-oxopyrrolidine-2-carboxamide (Compound 215); (S)-3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)benzofuran-7- yl)imidazolidine-4-carboxamide (Compound 216); (R)-3-Methyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-yl)ox y)benzofuran-7- yl)imidazoledine-4-carboxamide (Compound 217); (S)-3-Methyl-N-(1-methyl-6-((5-(trifluoromethyl)pyridin-2-yl )oxy)-1H-benzo- [d]imidazol-4-yl)-2-oxoimidazolidine-4-carboxamide (Compound 218); (R)-3-Methyl-N-(1-methyl-6-((5-(trifluoromethyl)pyridin-2-yl )oxy)-1H-benzo- [d]imidazol-4-yl)-2-oxoimidazolidine-4-carboxamide (Compound 219); (S)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 220); (R)-N-(4-Fluoro-2-methoxy-5-((5-(trifluoromethyl)pyridin-2-y l)oxy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 221); N-(5-(3,4-Dichlorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 222); N-(5-(3-Chloro-4-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxo- pyrrolidine-2-carboxamide (Compound 223); N-(5-(3,4-Difluorophenoxy)-2-(1,3,4-oxadiazol-2-yl)phenyl)-1 -methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 224); 1-Methyl-5-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-1H-indazol- 7-yl)- pyrrolidine-2-carboxamide (Compound 225); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,3-d imethyl-2- oxoimidazolidine-4-carboxamide (Compound 226); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,3-d imethyl-2- oxoimidazolidine-4-carboxamide (Compound 227); 4-Hydroxy-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl) -1-methyl-5- oxopyrrolidine-3-carboxamide (Compound 228); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo-1-( 5-oxopyrrolidi- ne-2-carbonyl)pyrrolidine-2-carboxamide (Compound 229); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(1-meth yl-5-oxo- pyrrolidine-2-carbonyl)-5-oxopyrrolidine-2-carboxamide (Compound 230); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo-1-( 4-oxoazetidine- 2-carbonyl)pyrrolidine-2-carboxamide (Compound 231); N-(5-(3,4-difluorophenoxy)-2-methoxyphenyl)-5-oxo-1-(4-oxoaz etidine-2- carbonyl)pyrrolidine-2-carboxamide (Compound 232); 1-Methyl-5-oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)pyrrolidine-2-carboxamide (Compound 233); 1-Methyl-5-oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)pyrrolidine-2-carboxamide, enantiomer 1 (Compound 234); 1-Methyl-5-oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihydro benzo[b][1,4]- dioxin-5-yl)pyrrolidine-2-carboxamide, enantiomer 2 (Compound 235); 1-Methyl-N-(8-methyl-7-(3-(trifluoromethyl)phenoxy)-2,3-dihy drobenzo[b]- [1,4]dioxin-5-yl)-5-oxopyrrolidine-2-carboxamide (Compound 236); 1-Methyl-5-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dihydro benzofuran-7- yl)pyrrolidine-2-carboxamide (Compound 237); 1-Methyl-5-oxo-N-(5-((3-(trifluoromethyl)benzyl)oxy)-2,3-dih ydrobenzofuran- 7-yl)pyrrolidine-2-carboxamide (Compound 238); N-(5-(3,4-Difluorophenoxy)-2,3-dihydrobenzofuran-7-yl)-1-met hyl-5-oxopyrro- lidine-2-carboxamide (Compound 239); N-(7-(3,4-Difluorophenoxy)-2,3-dihydrobenzo[b][1,4]dioxin-5- yl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 240); N-(7-(4-Fluorophenoxy)-2,3-dihydrobenzo[b][1,4]dioxin-5-yl)- 1-methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 241); N-(5-((3,4-Difluorophenoxy)methyl)-2,3-dihydrobenzofuran-7-y l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 242); N-(6-((3,4-Difluorophenoxy)methyl)-2,3-dihydrobenzofuran-4-y l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 243); 1-Methyl-N-(1-methyl-6-((5-(trifluoromethyl)pyridin-2-yl)oxy )-1H-benzo- [d]imidazol-4-yl)-5-oxopyrrolidine-2-carboxamide, enantiomer 1 (Compound 244); 1-Methyl-N-(1-methyl-6-((5-(trifluoromethyl)pyridin-2-yl)oxy )-1H-benzo- [d]imidazol-4-yl)-5-oxopyrrolidine-2-carboxamide, enantiomer 2 (Compound 245); N-(5-(((3-Fluorophenyl)amino)methyl)-2-methoxyphenyl)-5-oxop yrrolidine-2- carboxamide (Compound 246); N-(5-((4,4-Difluorocyclohexyl)oxy)-2-methoxyphenyl)-1-methyl -5-oxopyrro- lidine-2-carboxamide (Compound 247); N-(5-((3,4-Difluorobenzyl)oxy)-2,3-dihydrobenzofuran-7-yl)-1 -methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 248); N-(5-((3-Fluorophenoxy)methyl)benzofuran-7-yl)-1-methyl-5-ox opyrrolidine-2- carboxamide (Compound 249); N-(2-Fluoro-3-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 1-methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 250); N-(5-(3,4-difluorophenoxy)-2-fluoro-3-methoxyphenyl)-1-methy l-5-oxopyrro- lidine-2-carboxamide (Compound 251); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxotetr ahydropyrrolo- [2,1-b]thiazole-7a(5H)-carboxamide 1,1-dioxide (Compound 252); N-(3-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 253); (E)-N-(5-(3-Fluorostyryl)-2-methoxyphenyl)-1-methyl-5-oxopyr rolidine-2- carboxamide (Compound 254); N-(2-Methoxy-5-((4-(trifluoromethyl)cyclohexyl)oxy)phenyl)-1 -methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 255); N-(2-Methoxy-5-(3-(trifluoromethyl)benzyl)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 256); N-(2-Methoxy-5-(4-(trifluoromethyl)benzyl)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 257); N-(2-Chloro-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 258); N-(4-Methoxy-3-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 259); N-(5-(4-Fluorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 260); N-(3-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-2- carboxamide (Compound 261); N-(5-((6-Fluoro-5-methylpyridin-3-yl)oxy)-2-methoxyphenyl)-5 -oxopyrrolidine- 2-carboxamide (Compound 262); (R)-N-(5-((6-fluoro-5-methylpyridin-3-yl) oxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 263); N-(2-Methoxy-5-((4-(trifluoromethyl)cyclohexyl)oxy)phenyl)-1 -methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 264); (R)-N-(2-Methoxy-5-((4-(trifluoromethyl)cyclohexyl)oxy)pheny l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 265); N-(2-Methoxy-5-(((1R,3S)-3-(trifluoromethyl)cyclohexyl)oxy)p henyl)-5-oxo- pyrrolidine-2-carboxamide (Compound 266); N-(2-Methoxy-5-(((1S,3S)-3-(trifluoromethyl)cyclohexyl)oxy)p henyl)-5-oxo- pyrrolidine-2-carboxamide (Compound 267); (R)-N-(2-Methoxy-5-(((1R,3S)-3-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 268); (R)-N-(2-Methoxy-5-(((1S,3S)-3-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 269); N-(2-Fluoro-5-((4-(trifluoromethyl)cyclohexyl)oxy)phenyl)-1- methyl-5-oxo- pyrrolidine-2-carboxamide (Compound 270); (R)-N-(4-methoxy-3-(((1r,4R)-4-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 271); (R)-N-(4-Methoxy-3-(((1s,4S)-4-(trifluoromethyl)cyclohexyl)o xy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 272); N-(3-Methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 273); N-(3-(4-Chloro-3-(trifluoromethyl)phenoxy)-5-methoxyphenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 274); (R)-N-(3-((4,4-Difluorocyclohexyl)oxy)-5-methoxyphenyl)-1-me thyl-5-oxo- pyrrolidine-2-carboxamide (Compound 275); N-(2-methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 276); N-(3-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 277); (R)-N-(3-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-met hyl-5-oxo- pyrrolidine-2-carboxamide (Compound 278); N-(3-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 279); 1-Methyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)qu inolin-8-yl)- pyrrolidine-2-carboxamide (Compound 280); (R)-1-Methyl-5-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-yl)ox y)quinolin-8- yl)pyrrolidine-2-carboxamide (Compound 281); (R)-N-(3-Methoxy-5-((4-(trifluoromethyl)cyclohexyl)oxy)pheny l)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 282); (R)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 283); N-(3-(3,4-Difluorophenoxy)-5-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 284); (R)-N-(3-(3,4-Difluorophenoxy)-5-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (Compound 285); N-(5-(Cyclohexyloxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrolid ine-2- carboxamide (Compound 286); N-(5-(Cyclohex-2-en-1-yloxy)-2-methoxyphenyl)-1-methyl-5-oxo pyrrolidine-2- carboxamide (Compound 287); (S)-N-(5-((5-Chloropyridin-2-yl)oxy)-2-methoxyphenyl)-1-meth yl-5-oxo- pyrrolidine-2-carboxamide (Compound 288); 1-Acetyl-N-(2-methoxy-5-(3-(trifluoromethyl)phenoxy)phenyl)a zetidine-3- carboxamide (Compound 289); (R)-N-(2-Methoxy-5-(4-(trifluoromethoxy)phenoxy)phenyl)-1-me thyl-5-oxo- pyrrolidine-2-carboxamide (Compound 290); N-(2-methoxy-5-(3-(trifluoromethoxy)phenoxy)phenyl)-1-methyl -5-oxo- pyrrolidine-2-carboxamide (Compound 291); N-(5-(4-(Difluoromethyl)phenoxy)-2-methoxyphenyl)-1-methyl-5 -oxo- pyrrolidine-2-carboxamide (Compound 292); (R)-N-(5-(4-Fluoro-3-methoxyphenoxy)-2-methoxyphenyl)-1-meth yl-5-oxo- pyrrolidine-2-carboxamide (Compound 293); N-(5-(Cyclohexylmethoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrr olidine-2- carboxamide (Compound 294); N-(5-(3-Fluoro-4-methoxyphenoxy)-2-methoxyphenyl)-1-methyl-5 -oxo- pyrrolidine-2-carboxamide (Compound 295); N-(5-((4,4-Dimethylcyclohexyl)oxy)-2-methoxyphenyl)-1-methyl -5-oxo- pyrrolidine-2-carboxamide (Compound 296); N-(5-((3,4-Difluorophenyl)thio)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine- 2-carboxamide (Compound 297); N-(5-((3,4-Difluorophenyl)thio)-2-methoxyphenyl)-5-oxopyrrol idine-2- carboxamide (Compound 298); N-(5-(3-Bromophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrroli dine-2- carboxamide (Compound 299); N-(2-Methoxy-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-oxopyr rolidine-2- carboxamide (Compound 300); N-(5-(4-Isopropoxyphenoxy)-2-methoxyphenyl)-5-oxopyrrolidine -2- carboxamide (Compound 301); N-(5-((3,3-Difluorocyclobutyl)methoxy)-2-methoxyphenyl)-1-me thyl-5- oxopyrrolidine-2-carboxamide (Compound 302); N-(3-(4-Fluorophenoxy)-5-(trifluoromethyl)phenyl)-1-methyl-5 -oxopyrrolidine- 2-carboxamide (Compound 303); N-(5-(4-Chlorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 304); N-(5-(4-Chloro-3-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 305); N-(3-Cyano-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5- oxopyrrolidine- 2-carboxamide (Compound 306); (S)-N-(5-(4-Chlorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 307); (R)-N-(5-(4-Chlorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopy rrolidine-2- carboxamide (Compound 308); N-(5-(3-Chloro-4-cyanophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 309); (S)-N-(5-(3-Chloro-4-cyanophenoxy)-2-methoxyphenyl)-1-methyl -5-oxo- pyrrolidine-2-carboxamide (Compound 310); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(me thylsulfonyl)- pyrrolidine-2-carboxamide (Compound 311); (S)-N-(5-(4-Chloro-3-fluorophenoxy)-2-methoxyphenyl)-1-methy l-5-oxo- pyrrolidine-2-carboxamide (Compound 312); (S)-N-(5-(4-(Difluoromethyl)phenoxy)-2-methoxyphenyl)-1-meth yl-5-oxo- pyrrolidine-2-carboxamide (Compound 313); N-(2-Methoxy-5-((1-methyl-1H-indol-5-yl)oxy)phenyl)-1-methyl -5-oxo- pyrrolidine-2-carboxamide (Compound 314); N-(5-((2,3-Dihydrobenzofuran-5-yl)oxy)-2-methoxyphenyl)-1-me thyl-5- oxopyrrolidine-2-carboxamide (Compound 315); N-(5-(3-Chlorophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 316); N-(5-(4-Cyano-3-methylphenoxy)-2-methoxyphenyl)-1-methyl-5-o xo- pyrrolidine-2-carboxamide (Compound 317); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(2-meth oxyethyl)-5- oxopyrrolidine-2-carboxamide (Compound 318); (R)-N-(5-(4-(Difluoromethyl)phenoxy)-2-methoxyphenyl)-1-meth yl-5-oxo- pyrrolidine-2-carboxamide (Compound 319); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 6-oxo- piperidine-2-carboxamide (Compound 320); N-(5-(3,4-Difluorophenoxy)-2-methoxyphenyl)-1-methyl-6-oxopi peridine-2- carboxamide (Compound 321); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-2-oxopipe ridine-4- carboxamide (Compound 322); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 2-oxo- piperidine-4-carboxamide (Compound 323); N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -2-oxopiperidine- 4-carboxamide, enantiomer 1 (Compound 324); N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -2-oxopiperidine- 4-carboxamide, enantiomer 2 (Compound 325); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(methyl sulfonyl)- pyrrolidine-3-carboxamide (Compound 326); N-(2-methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -2-oxopiperidine- 4-carboxamide, enantiomer 1 (Compound 327); N-(2-Fluoro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 328); N-(2-Chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 329); N-(2-Carbamoyl-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methy l-5- oxopyrrolidine-2-carboxamide (Compound 330); N-(2-Methoxy-5-((4-(trifluoromethyl)-pyridin-2-yl)oxy)phenyl )-1-(2- methoxyacetyl)-5-oxopyrrolidine-2-carboxamide (Compound 331); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-met hyl-2-oxo- imidazolidine-4-carboxamide (Compound 332); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(2- methoxyacetyl)- 5-oxopyrrolidine-2-carboxamide (Compound 333); N-(5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-metho xyphenyl)-1-(2- methoxyacetyl)-5-oxopyrrolidine-2-carboxamide (Compound 334); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr olidine-3- carboxamide (Compound 335); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(2- methoxyacetyl)- pyrrolidine-2-carboxamide (Compound 336); (S)-1-(2-Amino-2-oxoethyl)-N-(2-methoxy-5-(4-(trifluoromethy l)phenoxy)- phenyl)pyrrolidine-2-carboxamide (Compound 337); (S)-N-(5-(4-Chloro-3-fluorophenoxy)-2-methoxyphenyl)-3-methy l-2-oxo- imidazolidine-4-carboxamide (Compound 338); (S)-N-(5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 339); (S)-N-(5-(4-(Difluoromethyl)phenoxy)-2-methoxyphenyl)-3-meth yl-2-oxo- imidazolidine-4-carboxamide (Compound 340); 2-(1,3-Dimethyl-2,5-dioxoimidazolidin-4-yl)-N-(2-methoxy-5-( 4-(trifluoro- methyl)phenoxy)phenyl)acetamide (Compound 341); (S)-3-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phen yl)-1-methyl-2- oxoimidazolidine-4-carboxamide (Compound 342); (S)-3-Acetyl-N-(5-((3-fluoro-5-(trifluoromethyl)pyridin-2-yl )oxy)-2-methoxy- phenyl)-1-methyl-2-oxoimidazolidine-4-carboxamide (Compound 343); N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl) -5- oxopyrrolidine-3-carboxamide carboxamide (Compound 344); (S)-N-(5-((3-Chloro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 345); (S)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-1,3- dimethyl-2-oxoimidazolidine-4-carboxamide (Compound 346); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-(2- methoxyacetyl)- pyrrolidine-2-carboxamide (Compound 347); (S)-N-(5-(3-Chlorophenoxy)-2-methoxyphenyl)-3-methyl-2-oxoim idazolidine-4- carboxamide (Compound 348); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-3-carboxamide (Compound 349); N-(5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-methoxyphenyl)- 5-oxopyrrolidi- ne-2-carboxamide (Compound 350); (S)-N-(3-Chloro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 351); N-(3-Chloro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 352); (S)-N-(5-(4-(Fluoromethyl)phenoxy)-2-methoxyphenyl)-3-methyl -2- oxoimidazolidine-4-carboxamide (Compound 353); Methyl 2-(2-((2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)carbam oyl)-5- oxopyrrolidin-1-yl)acetate (Compound 354); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo pyrrolidine-3- carboxamide (Compound 355); (S)-N-(5-(4-Chlorophenoxy)-2-methoxyphenyl)-3-methyl-2-oxoim idazolidine-4- carboxamide (Compound 356); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo pyrrolidine-3- carboxamide (Compound 357); (S)-1-Acetyl-N-(5-((3-fluoro-5-(trifluoromethyl)pyridin-2-yl )oxy)-2- methoxyphenyl)pyrrolidine-2-carboxamide (Compound 358); (S)-N-(5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)-1,3- dimethyl-2-oxoimidazolidine-4-carboxamide (Compound 359); (S)-1,3-Dimethyl-2-oxo-N-(6-((5-(trifluoromethyl)pyridin-2-y l)oxy)benzo[d]- [1,3]dioxol-4-yl)imidazolidine-4-carboxamide (Compound 360); (S)-N-(2,4-Difluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy) phenyl)-3-methyl- 2-oxoimidazolidine-4-carboxamide (Compound 361); (S)-N-(3-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phen yl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 362); (S)-N-(2-Fluoro-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-meth yl-5-oxo- pyrrolidine-2-carboxamide (Compound 363); (S)-1,3-Dimethyl-2-oxo-N-(5-((5-(trifluoromethyl)pyridin-2-y l)oxy)-2,3- dihydrobenzofuran-7-yl)imidazolidine-4-carboxamide (Compound 364); (S)-N-(2-Fluoro-5-(4-(trifluoromethyl)phenoxy)phenyl)-3-meth yl-2-oxo- imidazolidine-4-carboxamide (Compound 365); N-(2-Bromo-5-(3-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5- oxopyrrolidine- 2-carboxamide (Compound 366); N-(2-Cyano-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5- oxopyrrolidine- 2-carboxamide (Compound 367); N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 368); N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 369); (2S,4R)-4-Hydroxy-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy )- phenyl)pyrrolidine-2-carboxamide (Compound 370); (S)-1-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phen yl)-5- oxopyrrolidine-2-carboxamide (Compound 371); N-(2-Hydroxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5-oxo- pyrrolidine-2-carboxamide (Compound 372); (S)-N-(2-Hydroxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 373); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 6-oxo- piperazine-2-carboxamide (Compound 374); 4-Amino-5-((2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)a mino)-5- oxopentanoic acid (Compound 375); 1-Methyl-6-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dihydro benzofuran-7- yl)piperazine-2-carboxamide (Compound 376); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo -1-(1H-pyrazol- 4-yl)pyrrolidine-2-carboxamide (Compound 377); (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo -1-(1H-pyrazol- 4-yl)pyrrolidine-2-carboxamide (Compound 378); 1-(3-Amino-3-oxopropyl)-N-(2-methoxy-5-(4-(trifluoromethyl)p henoxy)- phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 379); (2S,4S)-4-Hydroxy-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy )phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 380); 1-Imino-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)he xahydro-1λ ⁶ - thiopyran-4-carboxamide 1-oxide (Compound 381); N-(4-Fluoro-2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 3-methyl-2- oxoimidazolidine-4-carboxamide (Compound 382); 1,4-Dimethyl-6-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dih ydrobenzofuran- 7-yl)piperazine-2-carboxamide (Compound 383); N-(5-(4-Amino-2-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 384); N-(5-(4-Chloro-2-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 385); N-(5-(3-Acetylphenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 386); N-(5-(3-Acetylphenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 387); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-2-oxo-2,3 -dihydro- oxazole-4-carboxamide (Compound 388); N-(3-(3,4-Difluorophenoxy)-6-methoxy-2-methylphenyl)-1-methy l-5- oxopyrrolidine-2-carboxamide (Compound 389); N-(5-(3-Cyanophenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrroli dine-2- carboxamide (Compound 390); N-(2-Methoxy-5-(3-methoxy-4-(trifluoromethyl)phenoxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 391); N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1H-tetraz ole-5- carboxamide (Compound 392); (R)-N-(2-Methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 393); (S)-N-(2-Methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 394); N-(2-Methoxy-5-(3-methoxy-4-(trifluoromethyl)phenoxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 395); N-(5-(4-Cyano-3-(trifluoromethyl)phenoxy)-2-methoxyphenyl)-1 -methyl-5- oxopyrrolidine-2-carboxamide (Compound 396); N-(5-(3-Cyano-4-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (Compound 397); (S)-N-(5-(2-Fluoro-4-(trifluoromethyl)phenoxy)-2-methoxyphen yl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 398); (N-(5-((5-Fluoro-6-(trifluoromethyl)pyridin-3-yl)oxy)-2-meth oxyphenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 399); N-(5-((6-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-metho xyphenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 400); (S)-N-(5-((6-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 401); (R)-N-(5-((6-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 402); (S)-N-(2-Methoxy-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phe nyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 403); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 2-oxo- imidazolidine-4-carboxamide (Compound 404); (R,E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2,3-dihydrobenz ofuran-7-yl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 405); (S,E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2,3-dihydrobenz ofuran-7-yl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 406); (S,E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2,3-dihydrobenz ofuran-7-yl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 407); (E)-N-(5-(2-(4,4-Difluorocyclohexyl)vinyl)-2-methoxyphenyl)- 1,3-dimethyl-2- oxoimidazolidine-4-carboxamide (Compound 408); ((S,E)-N-(6-(2-(4,4-Difluorocyclohexyl)vinyl)benzo[d][1,3]di oxol-4-yl)-3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 409); N-(2-hydroxy-5-(3-methoxy-4-(trifluoromethyl)phenoxy)phenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 410); N-(5-(2-Hydroxy-4-(trifluoromethyl)phenoxy)-2-methoxyphenyl) -1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 411); 1-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)p yrrolidine-3- carboxamide (Compound 412); 1-Acetyl-N-(5-(3-fluorophenoxy)-2-methoxyphenyl)pyrrolidine- 3-carboxamide (Compound 413); 1-Glycyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 5-oxopyrrolidi- ne-2-carboxamide, HCl (Compound 414); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)pyrrol idine-2- carboxamide (Compound 415); (S)-N-(5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2-m ethoxyphenyl)- pyrrolidine-2-carboxamide (Compound 416); (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-N,1-d imethyl-5- oxopyrrolidine-2-carboxamide (Compound 417); and tautomers and pharmaceutically acceptable salts thereof. Compounds of the invention may be administered to a patient in therapeutically effective amounts which range usually from about 0.5 to about 2000 mg, more typically form about 1 to about 500 mg, for example from about 2 to about 100 mg, daily depending on the age, sex, weight, ethnic group, condition of the patient, condition to be treated, administration route and the active ingredient used. The compounds of the invention can be formulated into dosage forms using the principles known in the art. The compound can be given to a patient as such or in combination with suitable pharmaceutical excipients in the form of tablets, granules, capsules, suppositories, emulsions, suspensions or solutions. Choosing suitable ingredients for the composition is a routine for those of ordinary skill in the art. Suitable carriers, solvents, gel forming ingredients, dispersion forming ingredients, antioxidants, colours, sweeteners, wetting compounds and other ingredients normally used in this field of technology may also be used. The compositions containing the active compound can be given enterally or parenterally, the oral route being the preferred way. The contents of the active compound in the composition is from about 0.5 to 100 %, typically from about 0.5 to about 20 %, per weight of the total composition. The compounds of the invention can be given to the subject as the sole active ingredient or in combination with one of more other active ingredients for treatment of a particular disease. In the treatment of diseases and conditions wherein inhibition of TEAD is desired, such as various cancers or chronic pain, a combination of therapeutic agents and/or other treatments (e.g., radiation therapy) is often advantageous. The second (or third) agent to be administered may have the same or different mechanism of action than the primary therapeutic agent. Accordingly, a compound of the invention may be administered in combination with other anti-cancer treatments useful in the treatment of cancers. For example, a compound of the invention can be packaged together with instructions that the compound is to be used in combination with other anti-cancer agents and treatments for the treatment of cancer. Similarly, a compound of the invention may be administered in combination with other pain reliever agents useful in the treatment of chronic pain. For example, a compound of the invention can be packaged together with instructions that the compound is to be used in combination with other anti-cancer agents and treatments for the treatment of cancer, or with other pain reliever agents and treatments for the treatment of chronic pain. The present invention further comprises combinations of a compound of the invention and one or more additional agents in kit form, for example, where they are packaged together or placed in separate packages to be sold together as a kit, or where they are packaged to be formulated together. According to one embodiment of the invention, the therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof is co-administered with one or more anti-cancer agents or pain reliever agents. The optional other anti-cancer agents which can be administered in addition to a compound of formula (I) or a pharmaceutically acceptable salt thereof include, but are not limited to, - chemotherapeutic agents (e.g. docetaxel and paclitaxel), - tyrosine kinase inhibitors including EGFR inhibitors (e.g. gefitinib and osimertinib), VEGFR inhibitors (e.g. bevacizumab) and FGFR inhibitors (e.g. erdafitinib); - immune checkpoint inhibitors (e.g. nivolumab and pembrolizumab), - epigenetic modulators (e.g. BET inhibitors and HDAC inhibitors), - mTOR inhibitors (e.g. everolimus); - AKT inhibitors (e.g. AZ5363); - radiopharmaceuticals (e.g. alpharadin); - GnRH/LHRH analogues (such as leuprorelin); - PI3K inhibitors (e.g. idelalisib); and - CDK4/6 inhibitors (e.g. ribocyclib) - steroidogenesis inhibitors (e.g. CYP17A1 inhibitors such as abiraterone acetate and seviteronel); and - a non-steroidal androgen receptor antagonist (e.g. enzalutamide, apalutamide and darolutamide). According to still another embodiment, the present invention provides a pharmaceutical combination comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof and at least one additional active ingredient selected from the list consisting of - chemotherapeutic agents (e.g. docetaxel and paclitaxel), - tyrosine kinase inhibitors including EGFR inhibitors (e.g. gefitinib and osimertinib), VEGFR inhibitors (e.g. bevacizumab) and FGFR inhibitors (e.g. erdafitinib); - immune checkpoint inhibitors (e.g. nivolumab and pembrolizumab), - epigenetic modulators (e.g. BET inhibitors and HDAC inhibitors), - mTOR inhibitors (e.g. everolimus); - AKT inhibitors (e.g. AZ5363); - radiopharmaceuticals (e.g. alpharadin); - GnRH/LHRH analogues (such as leuprorelin); - PI3K inhibitors (e.g. idelalisib); and - CDK4/6 inhibitors (e.g. ribocyclib) - steroidogenesis inhibitors (e.g. CYP17A1 inhibitors such as abiraterone acetate and seviteronel); and - a non-steroidal androgen receptor antagonist (e.g. enzalutamide, apalutamide and darolutamide), for simultaneous, separate or sequential administration. The above other therapeutic agents, when employed in combination with a compound of the invention can be used, for example, in those amounts indicated in the Physicians' Desk Reference (PDR) or as otherwise determined by one of ordinary skill in the art. The compounds of the invention can be prepared by a variety of synthetic routes analogously to the methods known in the literature using suitable starting materials. The present invention will be explained in more detail by the following experiments and examples. The experiments and examples are meant only for illustrating purposes and do not limit the scope of the invention defined in claims. EXAMPLES: Purification methods used: A) Reverse phase HPLC (water/acetonitrile, 2-8 min 0-65 %, 30 mL/min, column: SunFire 100*19 mm). B) Reverse phase HPLC (water/methanol, 2-8 min 0-65 %, 30 mL/min, column: SunFire 100*19 mm). C) Reverse phase HPLC (water/acetonitrile/formic acid, 2-10 min 0-40 %, 30 mL/min, column: SunFire 100*19 mm). D) Reverse phase HPLC (water/acetonitrile/ammonia, 2-8 min 0-65 %, 30 mL/min, column: SunFire 100*19 mm). E) Reverse phase HPLC (water/methanol/ammonia, 2-10 min 40-50 %, 30 mL/min, column: SunFire 100*19 mm). F) Reverse phase HPLC (water/acetonitrile/trifluoroacetic acid, 2-10 min 0-50 %, 30 mL/min, column: SunFire 100*19 mm). G) Reverse phase HPLC (water/methanol/ trifluoroacetic acid, 2-10 min 10-50 %, 30 mL/min, column: SunFire 100*19 mm). H) Preparative chiral HPLC (methanol/isopropanol, 50-50, 12 mL/min, column: ChiralpakAD-H (250*20 mm). I) Preparative chiral HPLC (methanol/IPA/Hexane, 25-25-50, 0.6 mL/min, column: Chiralpak IC (250*4.6 mm). J) Preparative chiral HPLC (methanol/CO ₂ , 50-50, 2 mL/min, column: ChiralpakAD-H (250*4.6 mm). Intermediate 1.5-Bromo-2-fluoro-4-methoxyphenyl formate To a solution of 5-bromo-2-fluoro-4-methoxybenzaldehyde (1.000 g, 1 eq., 4.291 mmol) in CHCl ₃ (20 mL) was added 3-chlorobenzoperoxoic acid (1.851 g, 2.5 eq., 10.73 mmol) at 4 °C followed by stirring for 30 min. The mixture was diluted with water (50 ml) and the resulted mixture was extracted with ethyl acetate (3×10 mL). The organic layers were combined, washed with saturated solution of NaHCO ₃ (2x10 mL) and brine (10 ml), dried over sodium sulfate, filtered and concentrated to give the title compound. ¹ H NMR (400 MHz, DMSO-d6) δ: 8.57 (s, 1H), 7.69 (dd, 1H), 7.29 (dd, 1H), 3.86 (d, 3H). The following intermediates were prepared according to the procedure described for Intermediate 1 from the starting materials indicated in the Table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 5.5-Bromo-2-fluoro-4-methoxyphenol Sodium hydroxide (1.606 g, 2.5 eq., 40.15 mmol) was added to a solution of 5- bromo-2-fluoro-4-methoxyphenyl formate (4.0 g, 1 eq., 16.06 mmol) in methanol (100 mL). The mixture was stirred at 25 °C for 12 h. Then the mixture was concentrated, diluted with 50 mL of water, acidified to pH 1 and extracted with ethyl acetate (3×30 mL). The combined organic phases were dried over Na ₂ SO ₄ and concentrated. The crude product was purified twice by column chromatography using hexane-MTBE and chloroform-acetonitrile systems to give the title compound (1.4 g, 6.0 mmol, 37 %, 95 % purity). ¹ H NMR (500 MHz, DMSO-d6) δ: 9.66 (s, 1H), 7.12 (d, 1H), 7.04 (d, 1H), 3.73 (s, 3H). The following intermediates were prepared according to the procedure described for Intermediate 4 from the starting materials indicated in the Table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 9.5-Methoxy-7-nitrobenzofuran 5-Methoxy-7-nitrobenzofuran-2-carboxylic acid (1 g, 1 eq., 4.22 mmol) and copper (201 mg, 0.75 eq., 3.16 mmol) were refluxed in quinoline (20 mL) for 30 min. After cooling to RT the mixture was filtered and the filtrate was poured to 2 N hydro- chloric acid and filtered. The obtained precipitate was concentrated three times with acetonitrile to give the title compound (710 mg, 3.5 mmol). ¹ H NMR (500 MHz, DMSO-d6) δ: 8.20 (s, 1H), 7.66 (d, 1H), 7.10 (s, 1H), 3.86 (s, 3H). Intermediate 10a.3-(4-Methoxy-2-nitrophenyl)-1-methyl-1H-pyrazole 1-Bromo-4-methoxy-2-nitrobenzene (0.272 g, 1.17 mmol), 1-methyl-3-(4,4,5,5- tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (244 mg, 1.17 mmol) and potassium phosphate (746 mg, 3.52 mmol) were mixed in dioxane (4 mL) and water (0.4 mL) under argon atmosphere and the mixture was heated to 100 °C. Then di(1-adamantyl)-n- butylphosphine (21.0 mg, 0.05 eq., 58.6 µmol) and (2'-amino-[1,1'-biphenyl]-2-yl)- ((methylsulfonyl)oxy)palladium (21.7 mg, 0.05 eq., 58.6 µmol) were added and the mixture was stirred for 14 h at 100 °C. After cooling to RT the mixture was concentrated in vacuum. The residue was dissolved in ethyl acetate (5 mL), washed with brine (2×5 mL), dried over sodium sulfate, filtered and concentrated in vacuum to give crude title compound (0.2 g, 0.73 mmol) which was used in the next step without further purification. LCMS: m/z 234.2 [M+H] ⁺ . Intermediate 10b.4-(1-Methyl-1H-pyrazol-3-yl)-3-nitrophenol 3-(4-Methoxy-2-nitrophenyl)-1-methyl-1H-pyrazole (1.2 g, 1 eq., 5.145 mmol) was mixed with pyridine HCl (2.973 g, 5 eq., 25.73 mmol) followed by stirring at 200 °C for 30 h. After cooling to RT the reaction mass was poured into water (10 mL) and extracted with ethyl acetate (3×20 mL). Combined organic phases were dried over sodium sulfate, filtered and concentrated to give the title compound (0.90 g, 3.7 mmol). ¹ H NMR (400 MHz, DMSO-d6) δ: 10.42 (s, 1H), 7.70 (d, 1H), 7.54 (d, 1H), 7.10 (d, 1H), 7.05 (dd, 1H), 6.33 (d, 1H), 3.81 (s, 3H). The following intermediate was prepared according to the procedure described for Intermediate 10b from the starting material indicated in the Table. Intermediate 12a. (4-Fluoro-3-methoxyphenoxy)triisopropylsilane To a stirred solution of 4-fluoro-3-methoxyphenol (6 g, 1 eq., 42.21 mmol) and imidazole (5.748 g, 2 eq., 84.43 mmol) in DCM (60 mL) at RT was added chlorotriiso- propylsilane (8.546 g, 9.487 mL, 1.05 eq., 44.33 mmol). The mixture was stirred for 16 h and then poured into saturated aqueous NH ₄ Cl (40 mL), followed by extraction with DCM (3×50 mL). The combined extracts were washed with brine (30 mL), dried over Na ₂ SO ₄ , and concentrated in vacuum to give the title compound (10.00 g, 30 mmol). ¹ H NMR (400 MHz, Chloroform-d) δ: 6.87 (dd,1H), 6.48 (dd, 1H), 6.34 (dt, 1H), 3.82 (s, 3H), 1.23 (dh, 3H), 1.08 (d, 21H). Intermediate 12b. (4-Fluoro-3-iodo-5-methoxyphenoxy)triisopropylsilane (4-Fluoro-3-methoxyphenoxy)triisopropylsilane (6.544 g, 1 eq., 21.93 mmol) and potassium 2-methylpropan-2-olate (2.706 g, 1.1 eq., 24.12 mmol) were mixed in THF (60 mL) under argon atmosphere and cooled to -78 °C. Butyl lithium (1.545 g, 9.647 mL, 2.5 molar, 1.1 eq., 24.12 mmol) was added dropwise at -78 °C. Then the mixture was stirred for 1 h at the same temperature. The solution of iodine (6.678 g, 1.2 eq., 26.31 mmol) in THF (20 mL) was added dropwise at -78 °C. After stirring at RT overnight, the mixture was cooled to -20 °C and aqueous solution of ammonium chloride (20 mL) was added dropwise. Then the solution was warmed to RT. EtOAc (70 mL) was added and the organic layer was washed with brine (2×30 mL), dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (hexane/MTBE) to give the title compound (2.0 g, 3.3 mmol). GCMS: m/z 424 [M] ⁺ . Intermediate 12c.4-Fluoro-3-iodo-5-methoxyphenol (4-Fluoro-3-iodo-5-methoxyphenoxy)triisopropylsilane (2.3 g, 1 eq., 5.420 mmol) was dissolved in THF (10 mL) and tetrabutylammonium fluoride (3.543 g, 13.55 mL, 1 molar, 2.5 eq., 13.55 mmol) was added dropwise. The mixture was stirred at RT for 16 h and then concentrated in vacuum. The residue was dissolved in EtOAc (20 mL), washed with water (2×5 mL), dried under sodium sulfate and concentrated in vacuum. The obtained residue was purified by flash chromatography (hexane/MTBE) to give the title compound (0.575 g, 1.9 mmol). ¹ H NMR (400 MHz, Chloroform-d) δ: 6.72 (t, 1H), 6.45 (dd, 1H), 4.86 (s, 1H), 3.82 (s, 3H). Intermediate 13.1-Methoxy-2-nitro-4-(4-(trifluoromethyl)phenoxy)benzene 4-Methoxy-3-nitrophenol (1 g, 1 Eq., 6 mmol), (4-(trifluoromethyl)phenyl)- boronic acid (2 g, 2 eq., 0.01 mol), pyridine (0.9 g, 1 mL, 2 eq., 0.01 mol), diacetoxy- copper (1 g, 1.05 eq., 6 mmol) and powdered molecular sieves 4Å (1 g) were suspended in dichloromethane (10 mL). The air was bubbled through the resulting solution for 30 min and the mixture was stirred at RT overnight. The mixture was filtered. The filtrate was washed with water (2×30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by method A to afford the title compound. LCMS: m/z 314.0 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 13 from the starting materials indicated in the Table. Where LCMS/GCMS data was not informative, the data is not shown.

Intermediate 48.2-Fluoro-1-iodo-3-methoxy-5-(4-(trifluoromethyl)phenoxy)- benzene 1-Fluoro-2-methoxy-4-(4-(trifluoromethyl)phenoxy)benzene (4.000 g, 1 eq., 13.97 mmol) and potassium 2-methylpropan-2-olate (1.725 g, 1.1 eq., 15.37 mmol) were mixed in THF (60 mL) and cooled to -78 °C under argon atmosphere. Butyl lithium (984.7 mg, 6.149 mL, 2.5 molar, 1.1 eq., 15.37 mmol) was added dropwise at -78 °C and the mixture was stirred for 2 h at the same temperature. A solution of iodine (4.256 g, 1.2 eq., 16.77 mmol) in THF (20 mL) was added dropwise at -78 °C. After stirring at RT overnight, the mixture was cooled to -20 °C and aqueous solution of ammonium chloride (10 mL) was added dropwise. Then the solution was warmed to RT. EtOAc (100 mL) was added and the organic layer was washed with brine (2×25 mL), dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (hexane/MTBE) to give the title compound (0.900 g, 2.0 mmol, 14 %, 90 % purity). Intermediate 49.6-Hydroxy-8-nitrochroman-4-one 6-Bromo-8-nitrochroman-4-one (2.00 g, 1 eq., 7.35 mmol), 4,4,4',4',5,5,5',5'- octamethyl-2,2'-bi(1,3,2-dioxaborolane) (2.24 g, 1.2 eq., 8.82 mmol) and potassium acetate (2.16 g, 3 eq., 22.1 mmol) were mixed in 1,4-dioxane (20 mL). Argon was bubbled into the solution at 25 °C for 1 h to remove any excess oxygen. PdCl ₂ (dppf)CH ₂ Cl ₂ (180 mg, 0.03 eq., 221 µmol) was added to the mixture under argon atmosphere. The mixture was heated to 80 °C and stirred for 3 h until the reaction was completed. The mixture was cooled to 25 °C and then filtered. The precipitate was washed with dioxane (15 mL). The filtered solutions were combined, concentrated and then transferred to a reactor. Hydrogen peroxide (4.29 g, 4.29 mL, 35 w-%, 6 eq., 44.1 mmol) was added and the mixture was heated to 50 °C and stirred for 40 min until the reaction was completed. Water (10 mL) was added to the mixture, and the mixture was extracted with DCM (2×50 mL). The organic phase was collected, washed with 15 % brine (2×15 mL) and extracted with 15 % Na ₂ CO ₃ (2×25 mL). The aqueous phase was collected and the pH value was adjusted to 4-5 with 3 M HCl. The aqueous phase was then extracted with ethyl acetate (2×50 mL). The organic phase was collected, dried over Na ₂ SO ₄ and concentrated under reduced pressure to obtain the title compound (810 mg, 3.6 mmol). LCMS: m/z 208.0 [M+H] ⁺ The following intermediate was prepared according to the procedure described for Intermediate 49 from the starting material indicated in the Table. Intermediate 51. (7-Nitrobenzo[d][1,3]dioxol-5-yl)methanol 7-Nitrobenzo[d][1,3]dioxole-5-carbaldehyde (1000 mg, 1 eq., 5.125 mmol) was dissolved in anhydrous methanol (40 mL). The mixture was cooled to 0 °C and sodium borohydride (232.6 mg, 1.2 eq., 6.150 mmol) was added portionwise during 10 min. The mixture was stirred at RT for 18 h and then concentrated under reduced pressure. The resulting residue was treated with saturated ammonium chloride solution (30 mL), extracted with ethyl acetate (3×20 mL), dried over anhydrous sodium sulphate, and concentrated under reduced pressure to give the title compound (0.693 g, 3.29 mmol, 64.1 %, 93.46 % purity). ¹ H NMR (500 MHz, DMSO-d6) δ: 7.50 (s, 1H), 7.21 (s, 1H), 6.28 (s, 2H), 5.41 (s, 1H), 4.45 (s, 2H). The following intermediates were prepared according to the procedure described for Intermediate 51 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 56.1-(Chloromethyl)-2,4-dimethoxy-5-nitrobenzene 2,4-Dimethoxy-1-nitrobenzene (1 g, 1 eq., 5 mmol), formaldehyde (0.3 g, 2 eq., 0.01 mol, aq.40 %) and zinc (II) chloride (0.07 g, 0.1 eq., 0.5 mmol) were dissolved in aqueous (37 %) hydrochloric acid (10 mL) followed by stirring at 100 °C for 12 h. After cooling to RT the reaction mixture was extracted with dichloromethane (2×50 mL), organic layers were combined, washed with water (2×100 mL), dried over sodium sulfate, filtered and concentrated in vacuum to give crude title compound (312 mg, 1.46 mmol, 30 %, 100 % purity), which was purified by method A. ¹ H NMR (400 MHz, DMSO-d ₆ ) δ: 7.97 (s, 1H), 6.81 (d, 1H), 4.43 (d, 2H), 4.01 (d, 1H), 3.96 (dd, 6H). The following intermediate was prepared according to the procedure described for Intermediate 56 from the starting material indicated in the table. Intermediate 58.5-(Chloromethyl)-1-fluoro-2-methoxy-3-nitrobenzene (3-Fluoro-4-methoxy-5-nitrophenyl)methanol (610 mg, 1 eq., 3.03 mmol) was dissolved in DCM (7 mL) and DMF (2.22 mg, 2.35 µL, 0.01 eq., 30.3 µmol) was added. The resulting solution was cooled to 0 °C and thionyl chloride (722 mg, 443 µL, 2 eq., 6.07 mmol) was added dropwise to the mixture at the same temperature and the solution was stirred at 0 °C for 10 min followed by warming to RT and stirring at this temperature overnight. The solution was then poured into 10 % aqueous sodium bicarbonate solution (10 mL) and stirred for 10 min. Then the aqueous layer was extracted with DCM (10 mL). Combined organic layers were dried over sodium sulfate, filtered and the solvent was evaporated under vacuum to give the title compound (602 mg, 2.4 mmol, 80 %, 88 % purity), which was used in the next step without further purification. LCMS: m/z 219.8 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 58 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 62. tert-Butyl (3-fluorophenyl)(4-methoxy-3-nitrobenzyl)- carbamate To a solution of tert-butyl (3-fluorophenyl)carbamate (1.048 g, 1 eq., 4.960 mmol) in DMF (20 mL) at 0 °C sodium hydride (238.1 mg, 60 %, 1.2 eq., 5.952 mmol) was added and the mixture was stirred at RT for 30 min.4-(Chloromethyl)-1-methoxy- 2-nitrobenzene (1.000 g, 1 eq., 4.960 mmol) was added in a single portion and the mixture was stirred at RT for 18 h. The resulting mixture was filtered, and the filtrate was diluted with water (50 mL) and ethyl acetate (50 mL). Layers were separated, the organic phase was washed with brine (4×30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure, to afford the title compound, which was used in the next step without further purification. The following intermediates were prepared according to the procedure described for Intermediate 62 from the starting materials indicated in the table. Intermediate 69.4-((3,4-Difluorophenoxy)methyl)-1-methoxy-2-nitrobenzene 3,4-Difluorophenol (2.00 g, 1 eq., 15.4 mmol) was dissolved in DMF (20 mL), sodium hydride (676 mg, 60 %, 1.1 eq., 16.9 mmol) was added at RT and the mixture was stirred at this temperature for 30 min.4-(Chloromethyl)-1-methoxy-2-nitrobenzene (3.41 g, 1.1 eq., 16.9 mmol) was added and the mixture was heated at 100 °C for 16 h. The solution was cooled to RT and concentrated. The residue was taken up in ethyl acetate (60 mL). The resulting solution was washed with brine (3×50 mL), dried over sodium sulfate, filtered and evaporated to give the title compound (4.5 g, 14 mmol, 94 %, 95 % purity). The crude product was used in the next step without further purification. The following intermediates were prepared according to the procedure described for Intermediate 69 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 75.4-(2,5-Difluorophenoxy)-1-methoxy-2-nitrobenzene 1,2,4-Trifluorobenzene (2.4 g, 1 eq., 18 mmol), 4-methoxy-3-nitrophenol (3.1 g, 1 eq., 18 mmol) and potassium 2-methylpropan-2-olate (2.2 g, 1.1 eq., 20 mmol) were dissolved in DMF (50 mL) and the resulting mixture was stirred at 80 °C for 10 h. Then EtOAc (50 mL) was added and the organic layer was washed with brine (5×30 mL), dried and evaporated under reduced pressure to afford title compound, which was used in the next step without further purification. GCMS: m/z 281 [M] ⁺ Intermediate 76. (E)-2-Methoxy-5-(2-(tetrahydro-2H-pyran-4-yl)vinyl)aniline 5-Bromo-2-methoxyaniline (730 mg, 1 eq., 3.61 mmol), (E)-4,4,5,5-tetramethyl- 2-(2-(tetrahydro-2H-pyran-4-yl)vinyl)-1,3,2-dioxaborolane (1.29 g, 1.5 eq., 5.42 mmol), sodium carbonate (383 mg, 1 eq., 3.61 mmol) and PdCl ₂ (dppf)-CH ₂ Cl ₂ adduct (295 mg, 0.1 eq., 361 µmol) were suspended in degassed 1,4-dioxane (12 mL) and water (2.4 mL). The mixture was heated under argon at 90 °C overnight. After cooling to RT the solvent was evaporated in vacuum, the residue was dissolved in ethyl acetate (30 mL), washed with brine (20 mL), dried over sodium sulfate, filtered, concentrated in vacuum and the residue was purified by method A to give the title compound (205 mg, 839 µmol, 23.2 %, 95.5 % purity). LCMS: m/z 234.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 76 from the starting materials indicated in the table. Intermediate 78.7-Bromo-5-((3,4-difluorobenzyl)oxy)-2,3-dihydrobenzofuran 7-Bromo-2,3-dihydrobenzofuran-5-ol (0.500 g, 1 eq., 2.33 mmol) was dissolved in N,N-Dimethylformamide (5 mL) and cesium carbonate (1.52 g, 2 eq., 4.65 mmol) was added. The mixture was stirred at RT for 10 min and 4-(chloromethyl)-1,2-difluoro- benzene (378 mg, 1 eq., 2.33 mmol) was added. The mixture was stirred at RT for 12 h. The resulting solution was concentrated under reduced pressure. The residue was taken up in ethyl acetate (20 mL). The obtained solution was washed with brine (20 mL), water (20 mL), dried over sodium sulfate, filtered and evaporated to afford the title compound. The crude product was used in the next step without further purification. ¹ H NMR (400 MHz, CDCl ₃ ) δ: 7.22 – 7.02 (m, 3H), 6.85 (s, 1H), 6.75 (s, 1H), 4.90 (s, 2H), 4.61 (t, 2H), 3.26 (t, 2H). The following intermediates were prepared according to the procedure described for Intermediate 78 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 84.1-Fluoro-2-((3-fluorophenoxy)methyl)-5-methoxy-4-nitro- benzene 1-(Chloromethyl)-2-fluoro-4-methoxy-5-nitrobenzene (0.306 g, 1 eq., 1.39 mmol) was dissolved in acetonitrile (3 mL), cesium carbonate (908 mg, 2 eq., 2.79 mmol) and sodium iodide (209 mg, 1 eq., 1.39 mmol) were added. The mixture was stirred for 10 min and 3-fluorophenol (141 mg, 114 µL, 0.9 eq., 1.25 mmol) was added. The mixture was stirred at RT for 10 h. The resulting solution was filtered and concentrated to give the title compound (0.362 g, 0.61 mmol, 44 %, 50 % purity), which was used in the next step without further purification. LCMS: m/z 297.2 [M+H] ⁺ Intermediate 85.1-Fluoro-5-methoxy-4-nitro-2-(3-(trifluoromethyl)phenoxy) - benzene 1,5-Difluoro-2-nitro-4-(3-(trifluoromethyl)phenoxy)benzene (150 mg, 1 eq., 470 µmol) was dissolved in toluene (2 mL). The solution was cooled to 0 °C, then methanol (15.1 mg, 19.0 µL, 1 eq., 470 µmol) was added at 0 °C. To the obtained solution potassium tert-butoxide (52.7 mg, 1 eq., 470 µmol) was added at 0 °C. The mixture was stirred at 0 °C for 10 minutes, then temperature was raised to RT followed by stirring for 12 h. The reaction mixture was quenched with water (15 mL) followed by stirring for 15 minutes. Toluene (10 mL) was added to the mixture. The layers were separated, and the aqueous layer was extracted with toluene (2×10 mL). Combined organic layers were washed with water (20 mL), brine (20 mL) and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford the title compound which was used in next step without further purification. GCMS: m/z 331.0 [M] ⁺ . Intermediate 86.7-Bromo-5-((3-fluorophenoxy)methyl)benzofuran A solution of (7-bromobenzofuran-5-yl)methanol (3.110 g, 1 eq., 13.70 mmol) and triphenylphosphine (4.311 g, 1.2 eq., 16.44 mmol) in THF (100 mL) was cooled to 0 °C under inert atmosphere. Diethyl (E)-diazene-1,2-dicarboxylate (2.863 g, 2.58 mL, 1.2 eq., 16.44 mmol) was slowly added and the mixture was stirred for 30 min followed by addition of 3-fluorophenol (1.612 g, 1.302 mL, 1.05 eq., 14.38 mmol). The ice-bath was removed and the mixture was stirred at RT for 17 h. The THF was evaporated, and the mixture was dissolved in MTBE (10 mL), washed with NaOH (3 mL, 10 %) and water (3 mL), dried over Na ₂ SO ₄ and concentrated in vacuo. The residue was purified by flash-chromatography (MTBE/hexane, flow rate 30 mL/min) to give the title compound (1.42 g, 4.2 mmol, 31 %, 95 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 8.03 (s, 1H), 7.72 (s, 1H), 7.59 (s, 1H), 7.33 – 7.23 (m, 1H), 7.03 (d, 1H), 6.83 (d, 2H), 6.75 – 6.65 (m, 1H), 5.17 (s, 2H). The following intermediates were prepared according to the procedure described for Intermediate 86 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown.

Intermediate 97.2-(4-Methoxy-3-nitrophenoxy)bicyclo[2.2.1]heptane 4-Methoxy-3-nitrophenol (5.00 g, 1 eq., 29.6 mmol), triphenylphosphine (15.5 g, 2 eq., 59.1 mmol) and bicyclo[2.2.1]heptan-2-ol (3.32 g, 1 eq., 29.6 mmol) were dissolved in THF (50 mL). The mixture was cooled to 4 °C and diisopropyl diazene- 1,2-dicarboxylate (12.0 g, 11.5 mL, 2 eq., 59.1 mmol) was added. The mixture was stirred at RT for 16 h, then concentrated and purified by flash-chromatography (MTBE/hexane, flow rate 30 mL/min) to afford the title compound. The following intermediate was prepared according to the procedure described for Intermediate 97 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown. Intermediate 99.4-(2,4-Difluorophenoxy)-1-methoxy-2-nitrobenzene 2,4-Difluoro-1-(4-methoxyphenoxy)benzene (0.180 g, 1 eq., 762 µmol) was dissolved in acetic acid (1 mL) and the solution was cooled to 0 °C. Then nitric acid (144 mg, 102 µL, 3 eq., 2.29 mmol) was added to the mixture dropwise and the resulting solution was stirred at RT for 10 h. Then the mixture was poured into ice- cooled saturated sodium carbonate solution (5 mL) and EtOAc (5 mL) was added. The organic layer was separated, dried over sodium sulfate and concentrated in vacuum to afford the title compound, which was used in the next step without further purification. GCMS: m/z 281 [M] ⁺ Intermediate 100.8-Nitrochroman-6-ol 8-Nitrochromane-4,6-diol (135 mg, 1 eq., 639 µmol) was dissolved in TFA (2 mL) and triethylsilane (372 mg, 0.511 mL, 5.00 eq., 3.20 mmol) was added. The mixture was stirred at 23 °C for 16 h, than concentrated, mixed with hexane (10 mL) and filtered. Obtained precipitate was dried under reduced pressure to give the title compound (100 mg, 0.49 mmol). The crude product was used in the next step without further purification. LCMS: m/z 196.0 [M+H] ⁺ Intermediate 101 and 102.4-Bromo-6-methoxy-1-methyl-1H-benzo[d]- imidazole and 7-Bromo-5-methoxy-1-methyl-1H-benzo[d]imidazole 7-Bromo-5-methoxy-1H-benzo[d]imidazole (0.3 g, 1 eq., 1.32 mmol) was dissolved in DMF (5 mL). The mixture was cooled to 5 °C and sodium hydride (58.1 mg, 60 w-%, 1.1 eq., 1.45 mmol) was added in portions. The mixture was stirred at 5 °C for 30 min and methyl iodide (206 mg, 90.9 µL, 1.1 eq., 1.45 mmol) was added dropwise at the same temperature. The resulting mixture was heated to 20 °C and stirred for 12 h, poured into ice-cooled water (10 mL) and extracted with EtOAc (2x20 mL). The combined organic layers were washed with brine (4x5 mL), dried and concentrated to give a mixture of crude products, which were separated by HPLC (Method A) to give two regioisomers 7-bromo-5-methoxy-1-methyl-1H-benzo[d]imidazole (0.0467 g, 194 µmol) and 4-bromo-6-methoxy-1-methyl-1H-benzo[d]imidazole (0.0868 g, 360 µmol). LCMS: m/z 243.0 [M+H] ⁺ . Intermediate 103.4-Bromo-1-methyl-1H-benzo[d]imidazol-6-ol 4-Bromo-6-methoxy-1-methyl-1H-benzo[d]imidazole (80 mg, 1 eq., 0.33 mmol) was dissolved in DCM (2 mL) and tribromoborane (0.83 g, 0.32 mL, 10 eq., 3.3 mmol) was added to the mixture dropwise at 4 °C. The resulting mixture was stirred at 28 °C for 18 h and the MeOH (5 mL) was added to the mixture at 4 °C dropwise. The mixture was concentrated under reduced pressure and the residue was poured into saturated aqueous sodium carbonate solution (10 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layer was dried over sodium sulfate and concentrated to give crude 4-bromo-1-methyl-1H-benzo[d]imidazol-6-ol (80 mg, 0.26 mmol) which was used in the next step without further purification. LCMS: m/z 227.0 [M+H] ⁺ Intermediate 104.2-(5-Bromo-2-fluoro-4-methoxyphenoxy)-5-(trifluoro- methyl)pyridine The mixture of 5-bromo-2-fluoro-4-methoxyphenol (4.75 g, 1 eq., 21.49 mmol), 2-fluoro-5-(trifluoromethyl)pyridine (3.548 g, 1 eq., 21.49 mmol) and cesium carbonate (14 g, 2 eq., 42.98 mmol) in DMF (100 mL) was stirred at 60 °C for 18 h. Water (100 mL) was added to the residue and the resulted mixture was extracted with ethyl acetate (100×20 mL). Organic layers were combined, washed with brine (4×100 mL), dried over sodium sulfate, filtered and evaporated to give crude title compound (6.35 g, 14.8 mmol) which was used in the next step without further purification. ¹ H NMR (400 MHz, Chloroform-d) δ: 8.38 (s, 1H), 7.91 (dd, 1H), 7.42 (d, 1H), 7.07 (d, 1H), 6.78 (d, 1H), 3.88 (s, 3H). Intermediate 105. Methyl 4-(3,4-difluorophenoxy)-2-nitrobenzoate Methyl 4-fluoro-2-nitrobenzoate (5.0 g, 1 eq., 25.11 mmol), 3,4-difluorophenol (3.593 g, 1.1 eq., 27.62 mmol) and potassium carbonate (6.940 g, 2 eq., 50.22 mmol) were mixed in acetonitrile (100 mL) followed by heating at reflux temperature for 14 h. After cooling to RT, the mixture was concentrated under reduced pressure, extracted with EtOAc (100 mL) and washed with water (20 mL), K ₂ CO ₃ solution (20 mL, 15 % in water) and brine (20 mL). The organic phase was dried over Na ₂ SO ₄ and concentrated in vacuum to give the title compound (6.68 g, 19 mmol, 77 %, 90 % purity). ¹ H NMR (500 MHz, DMSO-d6) δ: 7.89 (d, 1H), 7.63 (d, 1H), 7.59 – 7.50 (m, 1H), 7.47 (dq, 1H), 7.33 (dd, 1H), 7.12 – 7.03 (m, 1H), 3.81 (s, 3H). The following intermediates were prepared according to the procedure described for Intermediate 105 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown.

Intermediate 116.4-(3,4-Difluorophenoxy)-2-nitrobenzohydrazide To a solution of the methyl 4-(3,4-difluorophenoxy)-2-nitrobenzoate (2.000 g, 1 eq., 6.468 mmol) in ethanol (20 mL) was added hydrazine hydrate (2.266 g, 7 eq., 45.28 mmol). The mixture was heated under reflux overnight. Then the solvent was evaporated under reduced pressure, and water (20 mL) was added to the residue. The obtained solid was filtered, washed with water, hexane and dried in vacuum to give the title compound (1.900 g, 5.5 mmol, 85 %, 90 % purity). ¹ H NMR (500 MHz, DMSO- d6) δ: 9.77 (s, 1H), 7.59 (d, 1H), 7.59 – 7.49 (m, 2H), 7.47– 7.42 (m, 1H), 7.33 (dd, 1H), 7.07 – 6.99 (m, 1H), 4.32 (s, 1H). The following intermediates were prepared according to the procedure described for Intermediate 116 from the starting materials indicated in the table. Intermediate 119.2-(4-(3,4-Difluorophenoxy)-2-nitrophenyl)-1,3,4-oxadiazo le 4-(3,4-Difluorophenoxy)-2-nitrobenzohydrazide (1.000 g, 1 eq., 3.234 mmol), 4- methylbenzenesulfonic acid (111.4 mg, 0.2 eq., 646.8 µmol) and triethoxymethane (20 mL) were heated at reflux temperature for 14 h. The mixture was then concentrated in vacuum to give the title compound (1.00 g, 2.2 mmol, 69 %, 71 % purity) LCMS: m/z 320.0 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 119 from the starting materials indicated in the table. Intermediate 122. (E)-1-(4-(3,4-Difluorophenoxy)-2-nitrophenyl)-3-(dimethyl- amino)prop-2-en-1-one A solution of 1-(4-(3,4-difluorophenoxy)-2-nitrophenyl)ethan-1-one (0.300 g, 1 eq., 1.02 mmol), DMF-DMA (244 mg, 272 µL, 2 Eq, 2.05 mmol) and toluene (3 mL) was stirred and heated at reflux temperature for 16 h followed by cooling to RT. The resulting solid was filtered, washed with toluene, hexane and dried in vacuum to afford the title compound (0.246 g, 706 µmol, 69.0 %) as a yellow solid. LCMS: m/z 349.2 [M+H] ⁺ . Intermediate 123.5-(4-(3,4-Difluorophenoxy)-2-nitrophenyl)-1-methyl-1H- pyrazole (E)-1-(4-(3,4-Difluorophenoxy)-2-nitrophenyl)-3-(dimethylami no)prop-2-en-1- one (0.246 g, 1 eq., 706 µmol) and methylhydrazine sulfate (112 mg, 1.1 eq., 777 µmol) were mixed in 2-propanol (4 mL) and heated at reflux temperature for 18 h. The mixture was cooled to RT, concentrated in vacuum and purified by method C to give the title compound (0.109 g, 329 µmol, 46.6 %, 100 % purity). LCMS: m/z 332.0 [M+H] ⁺ . Intermediate 124.7-Nitro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-1H-inda zole To a stirred solution of 2-methyl-6-nitro-4-((5-(trifluoromethyl)pyridin-2-yl)- oxy)aniline (1.524 g, 1 eq., 4.865 mmol) in acetic acid (70.5 mL), a solution of sodium nitrite (369.2 mg, 1.1 eq., 5.352 mmol) in water (2.4 mL) was added and the mixture was stirred for 1 h. After completion of the reaction, acetic acid was distilled off and the obtained residue was mixed with ice water (200 mL) and extracted with MTBE (3×30 mL). The combined organic phase was washed with water (2×10 mL), dried under sodium sulfate and concentrated under reduced pressure to yield the title compound (1.5 g, 3.9 mmol, 80 %, 84 % purity). LCMS: m/z 325.0 [M+H] ⁺ . The following intermediate was prepared according to the procedure described for Intermediate 124 from the starting material indicated in the table. Intermediate 126.5-(4-(Trifluoromethyl)phenoxy)-1H-indazol-7-amine 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-7-nitro-1H-indazole (0.093 g, 1 eq., 0.26 mmol) was dissolved in methanol (15 mL). Formic acid, ammonia salt (0.33 g, 20 eq.., 5.2 mmol) and palladium (0.22 g, 10 w-%, 0.8 eq., 0.21 mmol) were added. The resulting mixture was stirred at 65 °C for 16 h, cooled to RT and filtered. The filtrate was concentrated under reduced pressure and treated with EtOAc (10 mL). The precipitate was filtered and dried under reduced pressure to give the title compound (0.044 g, 0.15 mmol, 58 %, 100 % purity) which was used in the next step without further purification. ¹ H NMR (500 MHz, DMSO-d6) δ: 7.87 (s, 1H), 7.65 (d, 2H), 7.06 (d, 2H), 6.62 (s, 1H), 6.18 (s, 1H), 5.69 (s, 2H). Intermediate 127.1-Methyl-7-nitro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy )- 1H-indazole To a solution of 7-nitro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)-1H-indazole (0.1 g, 1 eq., 308 µmol) in THF (4 mL) cooled to 0 °C sodium hydride (14.8 mg, 60 w- %, 1.2 eq., 370 µmol) was added. After stirring for 1 h at 23 °C, methyl iodide (46.0 mg, 20.3 µL, 1.05 eq., 324 µmol) was added dropwise at 0 °C. The mixture was stirred for 16 h at 23 °C. Water (1 mL) was added and the resulting mixture was concentrated under reduced pressure. The crude material was dissolved in EtOAc (10 mL), washed with water and brine, dried over MgSO _s and the solvent removed under reduced pressure to give the title compound (0.129 g, 310 µmol, 100 %, 81.2 % purity), which was used in the next step without further purification. LCMS: m/z 339.2 [M+H] ⁺ . Intermediate 128.1-(3,4-Difluorophenoxy)-4-methoxy-2-methyl-3-nitro- benzene A mixture of 1-Bromo-4-methoxy-2-methyl-3-nitrobenzene (0.384 g, 1.5 mmol), 3,4-difluorophenol (0.13 g, 1.0 mmol), Cs ₂ CO ₃ (0.652 g, 2.0 mmol), CuI (0.057 g, 0.3 mmol) and N,N-dimethylglycine (0.031 g, 0.3 mmol) in dioxane (5 ml) was heated at 130 °C for 24 hours. The mixture was evaporated and the residue was purified by normal phase chromatography to yield 0.175 g of the title compound. ¹ H NMR (400 MHz, DMSO-d6) δ: 2.07 (3 H, s), 3.87 (3 H, s), 6.71 - 6.79 (1 H, m), 7.12 - 7.19 (1 H, m), 7.19 - 7.27 (2 H, m), 7.38 - 7.49 (1 H, m). Intermediate 129.2-Methoxy-5-(4-(trifluoromethyl)phenoxy)aniline 1-Methoxy-2-nitro-4-(4-(trifluoromethyl)phenoxy)benzene (558 mg, 1 eq., 1.78 mmol) was dissolved in methanol (20 mL) and treated with Pd/C (37.9 mg, 0.2 eq., 356 µmol). The resulting mixture was hydrogenated at 1 atm pressure at RT overnight. The catalyst was filtered off and the solvent was evaporated under reduced pressure to afford the crude title product which was used in the next step without further purification. LCMS: m/z 284.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 129 from the starting material indicated in the table. Intermediate 158.2-(4-Methoxy-3-nitrophenoxy)-4-(trifluoromethyl)pyridine A mixture of 2-chloro-4-(trifluoromethyl)pyridine (2.72 g, 15.0 mmol), 4- methoxy-3-nitrophenol (2.80 g, 15.8 mmol) and Cs ₂ CO ₃ (5.68 g, 17.3 mmol) in DMF (20 ml) was heated at 100 ^° C for 7 h. Water was added (50 ml) and the mixture was extracted with EtOAc (3 x 50 ml). The organic layers were combined and evaporated to yield 4.71 g of the crude title compound which was used in the next reaction without further purification. ¹ H NMR (400 MHz, DMSO-d6) δ: 3.96 (3 H, s), 7.44 (1 H, d), 7.50 - 7.59 (3 H, m), 7.84 (1 H, d), 8.41 (1 H, d). LCMS: m/z 315.4 [M+H] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 158 from the starting material indicated in the table. Intermediate 163.2-Methoxy-5-((3-(trifluoromethyl)benzyl)oxy)aniline hydrochloride 1-Methoxy-2-nitro-4-((3-(trifluoromethyl)benzyl)oxy)benzene (8.70 g, 1 eq., 26.6 mmol), water (7.43 g, 7.4 mL, 15.5 eq., 412 mmol), ammonia hydrochloride (142 mg, 0.1 eq., 2.66 mmol) and hydrogen chloride (266 mg, 226 µL, 36.5 % aqueous, 0.1 eq., 2.66 mmol) were mixed in 1,4-dioxane (200 mL) followed by addition of iron (7.42 g, 5 eq., 133 mmol). The mixture was stirred at 110 °C for 5 h and at RT for 16 h. The mixture was filtered through thin layer of silica, concentrated and the residue was added to dioxane saturated with hydrochloric acid (30 mL). The solution was evaporated under reduced pressure. The obtained residue was washed with ethyl acetate and dried to give the title compound. LCMS: m/z 334.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 163 from the starting material indicated in the table.

Intermediate 182.5-((5-Chloropyridin-2-yl)oxy)-2-methoxyaniline 5-Chloro-2-(4-methoxy-3-nitrophenoxy)pyridine (197 mg, 1 eq., 702 µmol) was dissolved in methanol (5 mL) and platinum (20.5 mg, 0.15 eq., 105 µmol) was added. The mixture was degassed and stirred in atmosphere of hydrogen for 12 h, then filtered and the solvent was evaporated to give the title compound (175 mg, 0.66 mmol, 94 %, 95 % purity) which was used in next step without further purification. LCMS: m/z 251.0 [M+H] ⁺ . Intermediate 183.1,1-Diphenyl-N-(6-(3-(trifluoromethyl)phenoxy)benzo[d]- [1,3]dioxol-4-yl) methanimine 4-Bromo-6-(3-(trifluoromethyl)phenoxy)benzo[d][1,3]dioxole (1.20 g, 1 eq., 3.32 mmol), diphenylmethanimine (663 mg, 1.1 eq., 3.66 mmol), sodium 2-methyl- propan-2-olate (335 mg, 1.05 eq., 3.49 mmol) and 2,2'-bis(diphenylphosphino)-1,1'- binaphthyl (207 mg, 0.1 eq., 332 µmol) were dissolved in toluene (20 mL). The solution was bubbled with argon for 1 min, then diacetoxy palladium (37.3 mg, 0.05 eq., 166 µmol) was added and the mixture was stirred at 110 °C for 12 h in argon atmosphere. The mixture was filtered and the solid was washed with ethyl acetate (2×20 mL). Then ethyl acetate solution was washed with brine (2×50 mL). The organic phase was dried over sodium sulfate and filtered. Solvent was evaporated under reduced pressure to give title compound which was used in the next step without further purification. LCMS: m/z 462.0 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 183 from the starting material indicated in the table. Intermediate 189. tert-Butyl (7-(4-(trifluoromethyl)phenoxy)-2,3-dihydro- benzo[b][1,4]dioxin-5-yl)carbamate To a mixture of 5-bromo-7-(4-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b]- [1,4]dioxine (1.410 g, 1 eq., 3.759 mmol), tert-butyl carbamate (660.5 mg, 1.5 eq., 5.638 mmol) and cesium carbonate (3.674 g, 3 eq., 11.28 mmol) in toluene (40 mL) under argon XantPhos (326.2 mg, 0.15 eq., 563.8 µmol) and tris(dibenzylideneacetone)- dipalladium (172.1 mg, 0.05 eq., 187.9 µmol) were added and the mixture was heated at 110 °C for 18 h. After cooling to RT the mixture was filtered and concentrated. The residue was diluted with ethyl acetate (10 mL) and washed with brine (2×50 mL). The organic phase was dried over Na ₂ SO ₄ , filtered and concentrated in vacuum. The residue was recrystallized from acetonitrile to give the title compound. LCMS: m/z 412.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 189 from the starting materials indicated in the table. Where LCMS/GCMS data was not informative, the data is not shown.

Intermediate 202.7-(4-(Trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][1,4] dioxin-5-amine hydrochloride Chlorotrimethylsilane (1.320 g, 1.54 mL, 5 eq., 12.15 mmol) was added to methanol (25 mL) at 0 °C dropwise. The mixture was stirred for 30 min and tert-butyl (7-(4-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b][1,4]diox in-5-yl)carbamate (1 g, 1 eq., 2.431 mmol) was added and this solution was stirred at RT for 48 h. The mixture was concentrated in vacuum to give crude title compound (808 mg, 2.11 mmol, 86.9 %, 90.93 % purity). LCMS: m/z 312.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 202 from the starting material indicated in the table.

Intermediate 214.6-(3-(Trifluoromethyl)phenoxy)benzo[d][1,3]dioxol-4-amin e 1,1-Diphenyl-N-(6-(3-(trifluoromethyl)phenoxy)benzo[d][1,3]d ioxol-4-yl)- methanimine (0.800 g, 1 eq., 1.73 mmol) was dissolved in THF (10 mL) and HCl solution (253 mg, 6.93 mL, 1 molar, 4 eq., 6.93 mmol) was added at RT. A mixture was stirred at RT for 10 min and then evaporated in vacuum to give the title compound (640 mg, 1.1 mmol, 62 %, 50 % purity) which was used in the next step without further purification. LCMS: m/z 298.0 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 214 from the starting material indicated in the table. Intermediate 220.5-(2-Chloro-4-(trifluoromethyl)phenoxy)-4-fluoro-2- methoxyaniline hydrochloride tert-Butyl (5-(2-chloro-4-(trifluoromethyl)phenoxy)-4-fluoro-2-methoxy- phenyl)carbamate (0.185 g, 1 eq., 425 µmol) was dissolved in methanol (5 mL) and the solution of HCl (155 mg, 104 µL, 10 w-%, 1 eq., 425 µmol) in dioxane was added dropwise at 25 °C. The mixture was stirred at 25 °C for 56 h and then concentrated under reduced pressure to give the title compound (0.150 g, 0.32 mmol, 76 %, 80 % purity) which was used in the next step without further purification. ¹ H NMR (500 MHz, DMSO-d6) δ: 8.00 (s, 1H), 7.66 (d, 1H), 7.21 (d, 1H), 6.97 (m, 2H), 3.85 (s, 3H). LCMS: m/z 336.0 [M+H] ⁺ . Intermediate 221a. Methyl N-methylalaninate 1,1-dioxide Methyl alaninate 1,1-dioxide (350 mg, 1 eq., 2.12 mmol) and potassium carbonate (879 mg, 3 eq., 6.36 mmol) were mixed in anhydrous DMF (5 mL) followed by adding iodomethane (1.50 g, 660 µL, 5 eq., 10.6 mmol) in a single portion. The mixture was stirred at 27 °C for 18 h. The mixture was concentrated in vacuum, the residue was treated with water (5 mL) and the obtained suspension was extracted with ethyl acetate (2×20 mL). Combined organic phases were washed with brine (2×15 mL), dried over sodium sulfate, filtered and concentrated in vacuum to give the title compound (116 mg, 0.39 mmol, 18 %, 60 % purity) which was used in the next step without further purification. ¹ H NMR (500 MHz, DMSO-d6) δ: 4.56 – 4.46 (m, 1H), 4.38 (m, 1H), 3.95 (m, 1H), 3.71 (s, 3H), 2.67 (s, 3H). Intermediate 221b. Lithium N-methylalaninate 1,1-dioxide Methyl N-methylalaninate 1,1-dioxide (100 mg, 1 eq., 558 µmol) and lithium hydroxide hydrate (23.4 mg, 1 eq., 558 µmol) were dissolved in methanol (2 mL) and stirred at RT for 16 h. The mixture was concentrated and the residue was concentrated three times with acetonitrile to give the title compound (77 mg, 0.43 mmol, 77 %, 95 % purity) which was used in the next step without further purification. ¹ H NMR (400 MHz, DMSO-d6) δ: 4.10 – 3.96 (m, 2H), 3.13 (t, 1H), 2.61 (s, 3H). Intermediate 222a. tert-Butyl 1-methyl-5-thioxopyrrolidine-2-carboxylate To a solution of tert-butyl 1-methyl-5-oxopyrrolidine-2-carboxylate (470 mg, 1 eq., 2.36 mmol) in THF (3 mL) phosphorus (V) sulfide (262 mg, 0.5 eq., 1.18 mmol) was added. The mixture was refluxed with stirring for 24 h. The solution was cooled and filtered. Chloroform (20 mL) was added, and the organic phase was washed with saturated sodium hydrocarbonate, (20 mL). The aqueous phase was extracted with chloroform (20 mL). The combined organic phases were dried and concentrated under vacuum to give the title compound (500 mg, 1.8 mmol, 76 %, 77 % purity) which was used in next step without further purification. GCMS: m/z 216.1 [M] ⁺ . Intermediate 222b.1-Methyl-5-thioxopyrrolidine-2-carboxylic acid tert-Butyl 1-methyl-5-thioxopyrrolidine-2-carboxylate (500 mg, 1 eq., 2.32 mmol) was dissolved in trifluoroacetic acid (2.65 g, 1.79 mL, 10 eq., 23.2 mmol) and the solution was stirred at RT for 12 h. Then the solvent was evaporated and the residue was dissolved in toluene (5 mL) and concentrated to remove excess of TFA to give the title compound (370 mg, 1.2 mmol, 50 %, 50 % purity) which was used in the next step without further purification. Intermediate 223. N-(5-Hydroxy-2-methoxyphenyl)-1-methyl-5-oxo- pyrrolidine-2-carboxamide 1-Methyl-5-oxopyrrolidine-2-carboxylic acid (0.5 g, 1.2 eq., 3.49 mmol) was dissolved in N,N-dimethylformamide (5 mL) and HATU (1.33 g, 1.2 eq., 3.49 mmol) was added. The solution was stirred for 5 min at RT. To this solution, 3-amino- 4-methoxyphenol hydrochloride (511 mg, 1 eq., 2.91 mmol) was added, followed by the addition of DIPEA (1.05 g, 1.42 mL, 2.8 eq., 8.15 mmol). The mixture was then stirred at RT for 2 h. The solvent was removed in vacuum. The crude material was dissolved in ethyl acetate (10 mL), washed with brine (50 mL) and water (50 mL), dried and the solvent was evaporated. The residue was purified using method B to give the title compound (0.0667 g). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.34 (s, 1H), 8.96 (s, 1H), 7.54 (s, 1H), 6.85 (d, 1H), 6.45 (d, 1H), 4.42 (d, 1H), 3.32 (s, 2H), 2.66 (s, 3H), 2.37 – 2.11 (m, 3H), 1.87 (s, 1H). LCMS: m/z 265.2 [M+H] ⁺ . The following intermediate was prepared according to the procedure described for Intermediate 223 from the starting material indicated in the table. Intermediate 226. tert-Butyl (3-fluorophenyl)(4-methoxy-3-(5-oxopyrrolidine- 2-carboxamido)benzyl)carbamate To a mixture of tert-butyl (3-amino-4-methoxybenzyl)(3- fluorophenyl)carbamate (200 mg, 1 eq., 577 µmol), 5-oxopyrrolidine-2-carboxylic acid (74.5 mg, 1 eq., 577 µmol) and 1-methyl-1H-imidazole (237 mg, 5 eq., 2.89 mmol) in acetonitrile (4 mL) was added N-(chloro(dimethylamino)methylene)-N- methylmethanaminium hexafluorophosphate(V) (243 mg, 1.5 eq., 866 µmol). The mixture was stirred at RT for 18 h and then concentrated in vacuum. Water (20 mL) was added to the residue and the resulted mixture was extracted with ethyl acetate (2×20 mL). Organic layers were combined, washed with brine (20 mL), dried over sodium sulfate, filtered and evaporated to give the title compound (0.3 g) which was used in the next step without further purification. LCMS: m/z 358.0 [M+H] ⁺ . Intermediate 227a. Methyl 4-(methoxymethoxy)-2,3-dihydrobenzofuran-6- carboxylate To the solution of methyl 4-hydroxy-2,3-dihydrobenzofuran-6-carboxylate (2 g, 1 eq., 10.30 mmol) and N-ethyl-N-isopropylpropan-2-amine (3.994 g, 5.38 mL, 3 eq., 30.90 mmol) in DCM (80 mL) chloro(methoxy)methane (1.309 g, 1.24 mL, 95 w-%, 1.5 eq., 15.45 mmol) was added at 0 °C followed by stirring the mixture at 20 °C for 18 h. The mixture was washed with brine (3×10 mL), dried over sodium sulfate, filtered and evaporated to afford the title compound (2.3 g, 8.834 mmol, 85.78 %, 90.75 % purity) which was used in the next step without further purification. ¹ H NMR (500 MHz, Chloroform-d) δ: 7.29 (s, 1H), 7.13 (s, 1H), 5.23 (s, 2H), 4.63 (t, 2H), 3.87 (s, 3H), 3.49 (s, 3H), 3.20 (t, 2H). Intermediate 227b. (4-(Methoxymethoxy)-2,3-dihydrobenzofuran-6-yl)- methanol The solution of LiAlH4 (127 mg, 2 eq., 3.36 mmol) in THF (5 mL) was cooled to 0 °C and the solution of methyl 4-(methoxymethoxy)-2,3-dihydrobenzofuran-6- carboxylate (400 mg, 1 eq., 1.68 mmol) in THF (5 mL) was added dropwise. The cooling bath was removed and the mixture was stirred at 20 °C for 18 h. The mixture was cooled to 0 °C and water (130 µL) and 30 % solution of K ₂ CO ₃ (4×130 µL) were added dropwise. The mixture was filtered and the residue was washed by THF (5 mL). The organic layer was separated and concentrated to afford the crude title compound (340 mg, 1.48 mmol, 88.0 %, 91.31 % purity) as yellow oil, which was used in the next step without further purification. ¹ H NMR (400 MHz, Chloroform-d) δ: 6.59 (s, 1H), 6.48 (s, 1H), 5.17 (s, 2H), 4.66 – 4.48 (m, 4H), 3.47 (s, 3H), 3.14 (t, 2H). Intermediate 227c.5-((3,4-Difluorophenoxy)methyl)-4-(methoxymethoxy)-2,3- dihydrobenzofuran To the mixture of (7-(methoxymethoxy)-2,3-dihydrobenzofuran-5-yl)methanol (200 mg, 1 eq., 951 µmol) and 3,4-difluorophenol (124 mg, 1 eq., 951 µmol) in THF (40 mL) at 0 °C under Ar atmosphere were added tributylphosphane (385 mg, 0.48 mL, 2 eq., 1.90 mmol) and then (E)-diazene-1,2-diylbis(piperidin-1-ylmethanone) (480 mg, 2 eq., 1.90 mmol). The mixture was stirred at 20 °C for 18 h. The solvent of the mixture was evaporated under reduced pressure. The residue was purified by reverse phase HPLC (water-acetonitrile) to afford the title compound (178 mg, 552 µmol, 58.1 %). ¹ H NMR (500 MHz, Chloroform-d) δ: 7.04 (q, 1H), 6.83 – 6.71 (m, 1H), 6.64 (s, 2H), 6.54 (s, 1H), 5.19 (s, 2H), 4.92 (s, 2H), 4.60 (t, 2H), 3.49 (s, 3H), 3.17 (t, 2H). Intermediate 227d.5-((3,4-Difluorophenoxy)methyl)-2,3-dihydrobenzofuran-4 - ol Chlorotrimethylsilane (146 mg, 170 µL, 2 eq., 1.34 mmol) was added to MeOH (4 mL) at 0 °C dropwise. The mixture was stirred for 30 min and 5-((3,4-difluoro- phenoxy)methyl)-4-(methoxymethoxy)-2,3-dihydrobenzofuran (216 mg, 1 eq., 670 µmol) in MeOH (1 mL) was added followed by stirring at 20 °C for 18 h. The mixture was concentrated under reduced pressure to give crude title compound (178 mg, 623 µmol, 92.9 %, 97.37 % purity) as a beige solid. ¹ H NMR (500 MHz, DMSO-d6) δ: 9.50 (s, 1H), 7.34 – 7.27 (m, 1H), 7.14 – 7.01 (m, 1H), 6.83 – 6.73 (m, 1H), 6.34 (s, 1H), 6.28 (s, 1H), 4.92 (s, 2H), 4.47 (t, 2H), 2.99 (t, 2H). Intermediate 227e.6-((3,4-Difluorophenoxy)methyl)-2,3-dihydrobenzofuran-4 - yl trifluoromethanesulfonate To a solution of 5-((3,4-difluorophenoxy)methyl)-2,3-dihydrobenzofuran-4-ol (178 mg, 1 eq., 640 µmol) and triethylamine (84.2 mg, 116 µL, 1.3 eq., 832 µmol) in DCM (5 mL) trifluoromethanesulfonic anhydride (199 mg, 118 µL, 1.1 eq., 704 µmol) was added dropwise at 0 °C followed by stirring the mixture at 20 °C for 18 h. DCM (10 mL) was added to mixture and the solution was washed with NaHSO ₄ solution (2×5 mL), dried over sodium sulfate, filtered and evaporated to give the title compound (238 mg, 0.52 mmol, 82 %, 90 % purity) as a brown oil, which was used in the next step without further purification. ¹ H NMR (500 MHz, Chloroform-d) δ: 7.06 (q, 1H), 6.84 (s, 1H), 6.80 (s, 1H), 6.79 – 6.72 (m, 1H), 6.66 – 6.60 (m, 1H), 4.96 (s, 2H), 4.68 (t, 2H), 3.34 (t, 2H). Intermediate 228.2-Methoxy-5-(4-(trifluoromethyl)phenoxy)benzoic acid Solution of potassium hydroxide (51.6 mg, 1.5 eq., 919 µmol) in water (0.6 mL) was added to a solution of methyl 2-methoxy-5-(4-(trifluoromethyl)phenoxy)- benzoate (0.200 g, 1 eq., 613 µmol) in methanol (5 mL). The mixture was stirred for 16 h at 25 °C and then concentrated under reduced pressure. The residue was dissolved in water (5 mL) and washed with EtOAc (2×2 mL). The aqueous mixture was acidified with NaHSO ₄ (5 mL, 15 % in water). The resulting mixture was extracted with EtOAc (2×8 mL). The combined organic layers were dried under sodium sulfate and concentrated under reduced pressure to give the title compound (0.08 g, 0.26 mmol, 42 %). LCMS: m/z 311.0 [M-H]- _. Intermediate 229.1-Methoxy-3-nitro-5-(4-(trifluoromethyl)phenoxy)benzene 3-Methoxy-5-nitrophenol (0.5 g, 1 eq., 2.96 mmol), 4-trifluorophenylboronic acid (0.7 g, 1.5 eq., 4.43 mol), pyridine (1.2 g, 1.2 mL, 5 eq., 14.8 mol), diacetoxy- copper (0.54 g, 1 eq., 2.96 mmol) and powdered molecular sieves 4 Å (1 g) were suspended in DCM (15 ml). The air was bubbled through the resulting solution for 30 min and the mixture was stirred at RT overnight. The mixture was filtered, the filtrate was washed with water (2×30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by method A to afford the title compound. LCMS: m/z 314.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 229 from the starting material indicated in the table.

Intermediate 240.1-Methoxy-2-nitro-4-((4-(trifluoromethyl)cyclohexyl)oxy) - benzene To a mixture of 4-methoxy-3-nitrophenol (0.25 g, 1.47 mmol), 4-trifluoro- methyl-1-hydroxycyclohexane (0.20 ml, 1.47 mmol) and triphenylphosphine (465 mg, 1.77 mmol) in anhydrous THF (10 mL) under nitrogen was added DEAD (0.28 ml, 1.77 mmol) dropwise at RT and the mixture was left stirring for 24 h. The mixture was diluted with Et2O (30 ml) and washed with NaOH (2×10 ml), water (10 ml) and brine (10 ml). The organic phase was dried over sodium sulfate, filtered and concentrated. The crude residue was purified further with the purification method A to give 0.1 g of the title compound. LCMS: m/z 320.28 [M+H] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 240 from the starting material indicated in the table.

Intermediate 248. (E)-4-(3-Fluorostyryl)-1-methoxy-2-nitrobenzene Triethyl phosphine (5.6 ml, 32.6 mmol) was added to 3-fluorobenzyl bromide (2.0 ml, 16.3 mmol) at RT under N ₂ . The resulting mixture was heated at 150 °C for 2 h. The mixture was cooled and purified by flash chromatography to yield diethyl (3- fluorobenzyl)phosphonate. To the mixture of diethyl (3-fluorobenzyl)phosphonate (0.82 g, 3.3 mmol) in dry THF (10 ml) at 0 – 5 °C was added NaH (0.27 g, 11.0 mmol). After 30 min 4-methoxy-3-nitro benzaldehyde (0.5 g, 2.8 mmol) in dry THF (10 ml) was added dropwise to the mixture followed by stirred at RT for 3 h. The mixture was cooled, quenched with ice water (20 ml), made acidic with 2 M HCl and then extracted with ethyl acetate (2 x 10 ml). The combined organic layers were washed with water, dried, evaporated and then purified by flash chromatography to yield the title compound. LCMS m/z 274.2 [M+H] ⁺ . ¹ H NMR (Chloroform-d, 400 MHz) δ: 8.0-8.0 (m, 1H), 7.6- 7.7 (m, 1H), 7.2-7.4 (m, 4H), 6.9-7.1 (m, 3H), 3.99 (s, 3H). Intermediate 249.1-Methoxy-2-nitro-4-(3-(trifluoromethyl)benzyl)benzene

A mixture of 3-(trifluoromethyl)benzaldehyde (0.20 ml, 1.4 mmol) and toluene sulfonhydrazide (0.27 g, 1.4 mmol) in 1,4-dioxane (10 ml) was heated at 60 °C for 90 min. To the obtained crude product of (E)-4-methyl-N'-(3-(trifluoromethyl)benzylide- ne)benzenesulfonohydrazide (0.4 g, 1.168 mmol) was added K ₂ CO ₃ (0.24 g, 1.8 mmol) and 4-methoxy-3-nitrophenylboronic acid (0.23 g, 1.2 mmol). The mixture was heated under nitrogen atmosphere at 110 °C for 4 h followed by cooling to RT. The mixture was quenched with 2 M NaHCO ₃ (5 ml) and then extracted with ethyl acetate (2 x 10 ml). The combined organic layers were washed with water, dried, evaporated and purified by flash chromatography to yield the title compound. LCMS m/z 312.3 [M+H] ⁺ . ¹ H NMR (400 MHz, Chloroform-d) δ: 3.89 - 4.00 (m, 3 H), 4.02 (s, 2 H), 7.03 (d, 1 H), 7.27 - 7.35 (m, 3 H), 7.49 - 7.62 (m, 2 H), 7.65 - 7.70 (m, 1 H). Intermediate 250.1-Methoxy-2-nitro-4-(4-(trifluoromethyl)benzyl)benzene 1-Methoxy-2-nitro-4-(4-(trifluoromethyl)benzyl)benzene was prepared using the procedure described for Intermediate 234 using 4-(trifluoromethyl)benzaldehyde as starting material. LCMS m/z 312.3 [M+H] ⁺ . ¹ H NMR (400 MHz, Chloroform-d) δ: 3.90 - 4.04 (m, 5 H), 6.99 - 7.26 (m, 1 H), 7.32 - 7.34 (m, 1 H), 7.39 - 7.63 (m, 4 H), 7.69 (d, 1 H). Intermediate 251.1-Methoxy-2-nitro-4-(4-(trifluoromethyl)benzyl)benzene A mixture of 1-methoxy-3-nitro-5-(4-(trifluoromethyl)phenoxy)benzene (0.1 g, 1 eq., 0.32 mmol), zinc (0.21 g, 10 eq., 3.2 mmol), ammonium chloride (0.17 g, 10 eq., 3.2 mmol) in THF (5 ml), MeOH (2.5 ml) and water (2.5 ml) was stirred at RT for 4 h. The mixture was filtered through celite. The filtrate was washed with water (2×30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by flash chromatography to afford the title compound. LCMS m/z 284.1 [M] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 251 from the starting material indicated in the table.

Intermediate 290.2-Methoxy-5-(3-(trifluoromethoxy)phenoxy)aniline A mixture of 1-methoxy-2-nitro-4-(3-(trifluoromethoxy)phenoxy)benzene (0.050 g, 0.152 mol), zinc powder (0.050 g, 0.759 mmol), NH4Cl (0.041 g, 0.759 mmol), ethanol (1.5 ml) and water (0.5 ml) was stirred at 50 °C until the reaction was completed. The mixture was filtered through a pad of Celite. Celite layer was further washed with ethanol and the filtrate was evaporated to afford 0.040 g of the title compound. LCMS: m/z 299.8 [M+H] ⁺ . Intermediate 291.5-(4-Isopropoxyphenoxy)-2-methoxyaniline The compound was prepared according to the procedure of Intermediate 257 starting from 4-(4-isopropoxyphenoxy)-1-methoxy-2-nitrobenzene (0.22 g, 0.725 mmol) using 4 eq. of zinc powder and 4 eq. of NH ₄ Cl. Raw product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.044 g. LCMS: m/z 273.9 [M+H] ⁺ . Intermediate 292.2-Methoxy-5-(4-(trifluoromethoxy)phenoxy)aniline A mixture of 1-methoxy-2-nitro-4-(4-(trifluoromethoxy)phenoxy)benzene (0.12 g, 0.364 mol), iron powder (0.061 g, 1.093 mmol), anhydrous CaCl ₂ (0.040 g, 0.364 mmol), ethanol (1.0 ml) and water (0.25 ml) was stirred at 60 °C until the reaction was completed. The mixture was filtered through a pad of Celite. Celite layer was washed with EtOAc. The filtrate was washed with water (2x), dried and evaporated to afford 0.090 g of the title compound. LCMS: m/z 299.7 [M] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 292 from the starting material indicated in the table.

Intermediate 297.2-Amino-4-(4-(trifluoromethyl)phenoxy)benzamide The compound was prepared according to the procedure of Intermediate 292 starting from 2-nitro-4-(4-(trifluoromethyl)phenoxy)benzonitrile (0.36 g, 1.168 mmol). Raw product was purified by flash chromatography to afford the title compound. Yield: 0.21g. LCMS: m/z 296.8 [M] ⁺ . Intermediate 298.5-(Cyclohexylmethoxy)-2-methoxyaniline A mixture of 4-(cyclohexylmethoxy)-1-methoxy-2-nitrobenzene (0.26 g, 0.98 mol), zinc powder (0.32 g, 4.90 mmol, 5.0 eq.), NH4Cl (0.262 g, 4.90 mmol, 5.0 eq.), THF (3.0 ml), methanol (0.75 ml) and water (0.75 ml) was stirred at RT until the reaction was completed. The mixture was filtered through a pad of Celite. Celite layer was washed with EtOAc. The filtrate was washed with water (2x), dried and evaporated. Crude was purified by flash chromatography to afford 0.15 g of the title compound. LCMS: m/z 235.4 [M] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 298 from the starting material indicated in the table.

Intermediate 306.5-(3-Bromophenoxy)-2-methoxyaniline The compound was prepared using the procedure as described for Intermediate 298 starting from 4-(3-bromophenoxy)-1-methoxy-2-nitrobenzene (0.46 g, 1.419 mmol) using 7.5 eq. of zinc powder and 7.5 eq. of NH4Cl. Yield: 0.34 g. LCMS: m/z 294.2 [M] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 306 from the starting material indicated in the table. Intermediate 312.5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2- methoxyaniline The compound was prepared according to the procedure of Intermediate 298 starting from 3-fluoro-2-(4-methoxy-3-nitrophenoxy)-5-(trifluoromethyl)pyr idine (0.50 g, 1.505 mmol) using 10 eq. of zinc powder and 10 eq. of NH4Cl. Yield: 0.43 g. LCMS: m/z 303.5 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 312 from the starting material indicated in the table.

Intermediate 315.3-Amino-5-(4-(trifluoromethyl)phenoxy)benzonitrile To a mixture of 3-nitro-5-(4-(trifluoromethyl)phenoxy)benzonitrile (0.22 g, 0.714 mmol) in 1,4-dioxane (3.5 ml) was added tin(II) chloride dihydrate (0.805 g, 3.57 mmol) dissolved in 37 % aqueous HCl (1.0 ml). The mixture was stirred at RT until the reaction was completed. The mixture was made basic with 6 M NaOH solution. DCM was added and the mixture was filtered through a short plug of Celite. Celite was washed with DCM. Filtrate was dried and solvent evaporated to afford the title compound. Yield: 0.14 g. LCMS: m/z 279.3 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 315 from the starting material indicated in the table. Intermediate 319.1-Methoxy-2-nitro-4-(3-(trifluoromethoxy)phenoxy)benzene To a mixture of 4-methoxy-3-nitrophenol (0.169 g, 1.00 mmol), 3-(trifluoro- methoxy)phenylboronic acid (0.448 g, 2.18 mmol), anhydrous Cu(OAc) ₂ (0.182 g, 1.00 mmol) and powdered 4 Å molecular sieves (0.25 g) in dry DCM (7.5 ml) was added DIPEA (0.871 ml, 5.00 mmol). The mixture was stirred at RT until maximal conversion was obtained (48 h). The mixture was filtered through a plug of Celite and the Celite layer was washed with EtOAc. Filtrate was washed with 5 % aqueous NH ₄ OH solution, dried and evaporated. Crude was purified by reverse phase flash chromatography to afford 0.050 g of the title compound. LCMS: m/z 330.2 [M+H] ⁺ . Intermediate 320.1-Methoxy-2-nitro-4-(4-(trifluoromethoxy)phenoxy)benzene To a mixture of 4-methoxy-3-nitrophenol (0.338 g, 2.00 mmol), 4-(trifluoro- methoxy)phenylboronic acid (0.618 g, 3.00 mmol), anhydrous Cu(OAc) ₂ (0.363 g, 2.00 mmol) and powdered 4 Å molecular sieves (0.25 g) in dry DCM (15 ml) was added pyridine (0.809 ml, 10.0 mmol). The mixture was stirred at RT until maximal conversion was obtained (24-48 h). The mixture was filtered through a plug of Celite and the Celite layer was washed with DCM. Filtrate was washed with 5 % aqueous NH ₄ OH solution, dried and evaporated. Crude was purified by flash chromatography to afford 0.33 g of the title compound. LCMS: m/z 330.2 [M+H] ⁺ . The following intermediates were prepared according to the procedure described for Intermediate 320 from the starting material indicated in the table.

Intermediate 333.4-(Cyclohexylmethoxy)-1-methoxy-2-nitrobenzene To a cooled (0-5 ºC) mixture of cyclohexylmethanol (0.285 g, 2.50 mmol), 4- methoxy-3-nitrophenol (0.423 g, 2.50 mmol) and triphenylphosphine (0.984 g, 3.75 mmol) in dry THF (17 ml) was added diisopropyl azodicarboxylate (0.738 ml, 3.75 mmol). The mixture was stirred over night at RT. THF was evaporated and the residue was dissolved in DCM. Organic phase was washed with water and brine, dried and evaporated. Crude product was purified by flash chromatography to afford 0.26 g of the title compound. LCMS: m/z 266.2 [M+H] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 333 from the starting material indicated in the table. Intermediate 336.4-(4-(Difluoromethyl)phenoxy)-1-methoxy-2-nitrobenzene a) 4-(4-Methoxy-3-nitrophenoxy)benzaldehyde A mixture of 4-fluorobenzaldehyde (0.215 ml, 2.00 mmol), 4-methoxy-3-nitro- phenol (0.338 g, 2.00 mmol) and potassium carbonate (0.553 g, 4.00 mmol) in dry DMA (4.0 ml) was stirred at 120 ºC until the reaction was completed. Water was added to the cooled mixture and the mixture was extracted with EtOAc. Organic phase was washed with water, dried and evaporated to afford 0.49 g of the title compound. LCMS: m/z 274.1 [M+H] ⁺ . b) 4-(4-(Difluoromethyl)phenoxy)-1-methoxy-2-nitrobenzene 4-(4-Methoxy-3-nitrophenoxy)benzaldehyde (0.49 g, 1.793 mmol) was dissolved in dry DCM (5.5 ml) and cooled to 0-5 ºC. Diethylaminosulfur trifluoride (0.521 ml, 3.95 mmol) was added in small portions and the mixture was stirred at RT for 24 h. The mixture was diluted with DCM and saturated NaHCO ₃ solution was added in small portions. Phases were separated and aqueous phase was extracted with DCM. Combined organic phases were washed with water and brine, dried and evaporated. Crude was purified by flash chromatography to afford 0.37 g of the title compound. LCMS: m/z 296.0 [M+H] ⁺ . Intermediate 337. (3,4-Difluorophenyl)(4-methoxy-3-nitrophenyl)sulfane To a mixture of 3,4-difluorothiophenol (0.155 ml, 1.40 mmol), 4-methoxy-3- nitrophenylboronic acid (0.197 g, 1.00 mmol), copper(II) sulfate (8.0 mg, 0.05 mmol) and 1,10-phenanthroline (9.0 mg, 0.05 mmol) in ethanol (1.0 ml) (bubbled with oxygen before use) was added 40 % aqueous tetrabutylammoniumhydroxide (1.0 ml, 3.82 mmol). The mixture was stirred over night at RT. Then mixture was diluted with EtOAc and filtered through a pad of Celite. Celite layer was further washed with EtOAc. Filtrate was evaporated and crude was purified by flash chromatography to afford 0.17 g of the title compound. ¹ H NMR (400 MHz, CDCl ₃ ): δ 7.88 (d, 1H), 7.56 (dd, 1H), 7.00- 7.16 (m, 4H), 3.98 (s, 3H). Intermediate 338.2-Methoxy-5-(4-(trifluoromethyl)phenoxy)aniline a) 2-Chloro-1-(4-methoxy-3-nitrophenoxy)-4-(trifluoromethyl)ben zene A mixture of 2-chloro-1-fluoro-4-(trifluoromethyl)benzene (0.397 g, 2.00 mmol), 4-methoxy-3-nitrophenol (0.372 g, 2.20 mmol) and potassium carbonate (0.608 g, 4.40 mmol) in dry DMF (4.0 ml) was stirred at 120 °C until the reaction was completed. Water was added to the cooled mixture followed by stirring at RT for 1 h. The formed precipitate was filtered, washed with water and dried under reduced pressure to afford 0.62 g of the title compound. LCMS: m/z 348.1 [M+H] ⁺ . b) 2-Methoxy-5-(4-(trifluoromethyl)phenoxy)aniline To a mixture of 2-chloro-1-(4-methoxy-3-nitrophenoxy)-4-(trifluoromethyl)- benzene (0.66 g, 1.898 mmol) and ammonium formate (1.197 g, 18.98 mmol) in dry methanol (35 ml) was added 10 wt-% palladium on carbon (0.253 g, 0.237 mmol). The mixture was vigorously stirred at RT until the reaction was completed. The mixture was filtered through a plug of Celite and the Celite layer was washed with methanol. Filtrate was evaporated and the residue was dissolved in EtOAc. Organic phase was washed with water, dried and evaporated to afford 0.52 g of the title compound. LCMS: m/z 284.5 [M+H] ⁺ . Intermediate 339.2-Chloro-4-(4-methoxy-3-nitrophenoxy)benzonitrile A mixture of 4-methoxy-3-nitrophenol (0.677 g, 4.00 mmol, 1.0 eq.), 2-chloro- 4-fluorobenzonitrile (0.622 g, 4.00 mmol, 1.0 eq.) and potassium carbonate (1.216 g, 8.80 mmol, 2.2 eq.) in dry DMF (5.5 ml) was stirred at 100-120 ºC until reaction was completed. Cooled mixture was treated with water and the formed precipitate was filtered and dried to afford the title compound. Yield: 1.06 g. LCMS: m/z 304.5 [M+H] ⁺ . If the product did not precipitate from water, it was extracted with EtOAc. Organic phase was washed with water, dried and evaporated to afford the title compound which was used as such or purified by flash chromatography. The following intermediates were prepared according to the procedure described for Intermediate 339 from the starting material indicated in the table.

Intermediate 348.2-Nitro-4-(4-(trifluoromethyl)phenoxy)benzonitrile A mixture of 4-(trifluoromethyl)phenol (0.40 g, 2.467 mmol), 4-fluoro-2-nitro- benzonitrile (0.40 g, 2.408 mmol) and potassium carbonate (0.666 g, 4.82 mmol) in dry DMA (5.0 ml) was stirred at 100 ºC until the reaction was completed. Cooled mixture was diluted with water and extracted with EtOAc. Organic phase was dried and evaporated. Crude was purified by flash chromatography to afford the title compound. Yield: 0.40 g. ¹ H NMR (400 MHz, CDCl ₃ ) δ: 7.89 (d, 1H), 7.87 (d, 1H), 7.74-7.79 (m, 2H), 7.36 (dd, 1H), 7.20-7.25 (m, 2H). Intermediate 349.3-Nitro-5-(4-(trifluoromethyl)phenoxy)benzonitrile A mixture of 4-(trifluoromethyl)phenol (0.324 g, 2.00 mmol), 3,5-dinitrobenzo- nitrile (0.463 g, 2.40 mmol) and potassium phosphate (0.849 g, 4.00 mmol) in dry DMA (3.0 ml) was stirred at 100 ºC until the reaction was completed. Cooled mixture was diluted with water and extracted with EtOAc. Organic phase was dried and evaporated. Crude was purified by flash chromatography to afford the title compound. Yield: 0.42 g. LCMS: m/z 309.2 [M+H] ⁺ . Intermediate 350.4-(4-(Fluoromethyl)phenoxy)-1-methoxy-2-nitrobenzene a) (4-(4-Methoxy-3-nitrophenoxy)phenyl)methanol To a mixture of 4-(4-methoxy-3-nitrophenoxy)benzaldehyde (0.98 g, 3.59 mmol) in MeOH (15 ml) was added NaBH ₄ (0.204 g, 5.38 mmol) in small portions and stirred at RT until the reaction was completed. Solvent was evaporated and the residue was treated with water and EtOAc. Phases were separated and the aqueous phase was extracted with EtOAc. Combined organic phases were washed with water and brine, dried and evaporated to afford the title compound. Yield 0.97 g. LCMS: m/z 258.3 [M- H ₂ O+H] ⁺ . b) 4-(4-(Fluoromethyl)phenoxy)-1-methoxy-2-nitrobenzene To a cooled (-78 ºC) solution of (4-(4-methoxy-3-nitrophenoxy)phenyl)methanol (0.48 g, 1.744 mmol) in dry DCM (5.0 ml) was added diethylaminosulfur trifluoride (DAST) (0.25 ml, 1.892 mmol). Cooling bath was removed and the mixture was allowed to warm to RT and stirred until the reaction was completed. The mixture was diluted with DCM (15 ml) and cooled to 0-5 ºC. Saturated NaHCO ₃ solution (5 ml) was added to adjust pH to 7-8. Phases were separated and aqueous phase was extracted with DCM. Combined organic phases were washed with water and brine, dried and evaporated. Crude product was purified by flash chromatography to afford the title compound. Yield: 0.26 g. ¹ H NMR (400 MHz, CDCl ₃ ) δ: 7.53 (d, 1H), 7.36-7.41 (m, 2H), 7.25 (dd, 1H), 7.08 (d, 1H), 6.98-7.03 (m, 2H), 5.35 (d, 2H), 3.96 (s, 3H). Intermediate 351.2,4-Difluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)ani line A mixture of 5-amino-2,4-difluorophenol (0.218 g, 1.50 mmol) and potassium tert-butoxide (0.185 g, 1.65 mmol) in dry DMSO (3.0 ml) was stirred at RT for 1 h.2- Chloro-5-(trifluoromethyl)pyridine (0.272 g, 1.50 mmol) and K ₂ CO ₃ (0.104 g, 0.75 mmol) were added and stirring was continued at 120 ºC until the reaction was completed. Cooled mixture was diluted with water and extracted with EtOAc. Organic phase was washed with 1 M NaOH and water, dried and evaporated. Crude product was purified by filtration through a short plug of silica gel eluting with EtOAc-heptane (4:1). Filtrate was evaporated and the residue dried under vacuum to afford the title compound. Yield: 0.25 g. LCMS: m/z 291.5 [M+H] ⁺ . Intermediate 352. Benzyl (2S,4R)-4-hydroxy-2-((2-methoxy-5-(4-(trifluoro- methyl)phenoxy)phenyl)carbamoyl)pyrrolidine-1-carboxylate To a mixture of 2-methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (0.085 g, 0.30 mmol), (2S,4R)-1-((benzyloxy)-carbonyl)-4-hydroxypyrrolidine-2-carb oxylic acid (0.080 g, 0.30 mmol) in EtOAc (0.40 ml) and pyridine (0.20 ml) was added 1-propane- phosphonic acid cyclic anhydride, 50 wt-% in EtOAc (0.30 ml, 0.509 mmol). The mixture was stirred at RT overnight. The reaction was quenched with 0.5 % HCl- solution and diluted with water and EtOAc. Phases were separated and organic phase was washed with 0.5 % HCl-solution, water and brine, dried and evaporated to afford the title compound. Yield: 0.111 g. LC-MS: m/z= 531.3 [M+H] ⁺ . Crude product was used as such or purified by reverse phase flash chromatography to afford the pure compound. The following intermediates were prepared according to the procedure described for Intermediate 352 from the starting material indicated in the table.

Intermediate 357. tert-Butyl 1-(2-methoxyacetyl)-5-oxopyrrolidine-2- carboxylate To a cooled (0-5 ºC) mixture of tert-butyl 5-oxopyrrolidine-2-carboxylate (0.37 g, 2.00 mmol) in dry THF (5.0 ml) was added 60 wt-% NaH in oil (0.10 g, 2.50 mmol) followed by stirring at 0-5 ºC for 30 min.2-Methoxyacetyl chloride (0.26 g, 2.40 mmol) dissolved in dry THF (2.5 ml) was added and stirring continued at RT overnight. Solvent was evaporated and the residue treated with DCM and water. Phases were separated and the organic phase was washed with water and brine. Organic phase was dried and evaporated to afford the title compound. Yield: 0.51 g. LCMS: m/z 258.0 [M+H] ⁺ . Crude product was used as such or purified by reverse phase flash chromatography to afford the pure compound. The following intermediates were prepared according to the procedure described for Intermediate 357 from the starting material indicated in the table.

Intermediate 362. tert-Butyl (2-methoxyacetyl)-L-prolinate To a cooled (0-5 ºC) solution of tert-butyl L-prolinate (0.342 g, 2.00 mmol) and triethylamine (0.558 ml, 4.00 mmol) in dry DCM (10 ml) was added 2-methoxyacetyl chloride (0.239 g, 2.20 mmol). The mixture was stirred overnight at RT. The mixture was filtered and the filtrate was washed with saturated NH4Cl solution, saturated NaHCO ₃ solution, and brine, dried and evaporated to afford the title compound. Yield: 0.34 g. LCMS: m/z 244.2 [M+H] ⁺ . Intermediate 363. tert-Butyl (2-methoxyacetyl)-L-prolinate A mixture of tert-butyl L-prolinate (0.342 g, 2.00 mmol), 2-bromoacetamide (0.331 g, 2.40 mmol) and potassium hydrogencarbonate (0.30 g, 3.00 mmol) in dry acetonitrile (10 ml) was stirred at 80 ºC until the reaction was completed. Cooled mixture was filtered and the filtrate evaporated. Residue was treated with water and DCM. Phases were separated and the aqueous phase was extracted with DCM. Combined organic phases were dried and evaporated to afford the title compound. Yield: 0.34 g. LCMS: m/z 229.4 [M+H] ⁺ . Intermediate 364. (S)-1-(2-Methoxyacetyl)-5-oxopyrrolidine-2-carboxylic acid To a mixture of tert-butyl (S)-1-(2-methoxyacetyl)-5-oxopyrrolidine-2- carboxylate (0.77 g, 2.99 mmol) in dry DCM (15 ml) was added trifluoroacetic acid (2.50 ml, 32.4 mmol, 10.8 eq) followed by stirring overnight at RT. Solvent was evaporated and the residue was treated with toluene and evaporated again. This procedure was repeated and residue was dried under vacuum to afford the title compound. The crude product was either: (a) used in the next step as such or (b) extracted with DCM after basification with saturated Na2CO3 solution followed by drying and evaporating the organic phase. LCMS: m/z 201.9 [M+H] ⁺ The following intermediates were prepared according to the procedure described for Intermediate 364 from the starting material indicated in the table.

Intermediate 371. (E)-5-(2-(4,4-Difluorocyclohexyl)vinyl)-2,3-dihydrobenzo- furan-7-amine A mixture of 5-bromo-2,3-dihydrobenzofuran-7-amine (0.158 g, 0.738 mmol), 2-[(E)-2-(4,4-difluorocyclohexyl)ethenyl]-4,4,5,5-tetramethy l-1,3,2-dioxaboro- lane (0.243 g, 1.15 mmol), K ₃ PO ₄ (0.313 g, 2.0 mmol) and SPhos Pd G2 (0.040 g, 0.075 mmol) in dioxane (1 ml) and water (1 ml) was heated under nitrogen atmosphere at 85 ^° C for 8 h. The mixture was extracted with ethyl acetate (2 x 4 ml). The combined organic layers were evaporated and then purified by normal phase chromatography to yield 0.144 g of the title compound. ¹ H NMR (400 MHz, DMSO-d6) δ: 1.34 - 1.46 (2 H, m), 1.76 - 1.95 (4 H, m), 1.97 - 2.09 (2 H, m), 2.20 - 2.29 (1 H, m), 3.08 (2 H, t), 4.47 (2 H, t), 4.57 (2 H, s), 5.88 - 5.95 (1 H, m), 6.21 (1 H, d), 6.50 (1 H, d), 6.53 (1 H, br s). LCMS: m/z 280.7 [M+H] ⁺ The following intermediate was prepared according to the procedure described for Intermediate 371 from the starting material indicated in the table.

Intermediate 373.1-(((Benzyloxy)carbonyl)glycyl)-5-oxopyrrolidine-2- carboxylic acid a) 4-Nitrophenyl ((benzyloxy)carbonyl)glycinate Triethylamine (290 mg, 2.87 mmol, 1.2 eq.) was added to a suspension of the N- carbobenzyloxyglycine (1 eq.) in anhydrous CH ₂ Cl ₂ (12 mL). The stirred mixture was cooled to 0 °C and 4-nitrophenyl chloroformate (578 mg, 2.87 mmol, 1.2 eq.) was added. After 10 min, DMAP (29.2 mg, 0.239 mmol, 0.1 eq.) was added and the mixture was stirred at 0 °C for 1 h. The mixture was further diluted with CH ₂ Cl ₂ (20 mL) and washed with saturated NaHCO ₃ solution (10 mL), 0.1 M HCl solution (10 mL), brine (10 mL), and then dried (Na ₂ SO ₄ ), filtered and evaporated in vacuum to give the crude product. The crude residue was purified further with reversed phase chromatography to _{obtain the title compound. LCMS: m/z 331.068 (M+H)} ⁺ _. b) tert-Butyl 1-(((benzyloxy)carbonyl)glycyl)-5-oxopyrrolidine-2-carboxyla te LiHMDS (896 μL, 0.896 mmol, 1.06 eq.) was added dropwise to a solution of 5- oxo-2-pyrrolidinecarboxylic acid tert-butyl ester (157 mg, 0.845 mmol, 1 eq.) in anhydrous THF (3 ml) at -78 °C under nitrogen. The mixture stirred at RT for 15 min followed by the addition of a solution of 4-nitrophenyl ((benzyloxy)carbonyl)glycinate in anhydrous THF (4 ml) at -78 °C. The mixture was stirred for 1 h at this temperature. The mixture was diluted with ethyl acetate (20 ml) and washed with NH ₄ Cl (10 ml), brine (10 ml) and then dried (Na ₂ SO ₄ ), filtered and solvent evaporated in vacuum to give the crude product. The crude residue was purified further with reverse phase chromatography to obtain the title compound. LCMS: m/z 377.155 (M+H)+.  c) 1-(((Benzyloxy)carbonyl)glycyl)-5-oxopyrrolidine-2-carboxyli c acid (intermediate 373) Trifluoroacetic acid was added dropwise to a solution of tert-butyl 1- (((benzyloxy)carbonyl)glycyl)-5-oxopyrrolidine-2-carboxylate (285 mg, 0.76 mmol, 1 eq.) in anhydrous DCM under nitrogen at 0 °C. The mixture was stirred at 0 °C for 2 h. DCM and trifluoroacetic acid residue were removed in vacuum to give the crude product. The crude residue was purified further with reverse phase chromatography to obtain the title compound. LCMS: m/z 321.031 (M+H)+.  Example 1. N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo- pyrrolidine-2-carboxamide (Compound 1) To a solution of 2-methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (215 mg, 1 eq., 759 µmol) in anhydrous acetonitrile (5 mL) were added 5-oxopyrrolidine-2- carboxylic acid (98.0 mg, 1 eq., 759 µmol) and 1-methyl-1H-imidazole (312 mg, 5 eq., 3.80 mmol). The mixture was stirred at RT for 10 min and N,N,N',N'-tetramethylchloro- formamidinium hexafluorophosphate (319 mg, 1.5 eq., 1.14 mmol) was added in a single portion. The resulting solution was stirred at RT overnight and the mixture was directly purified by method A to afford the title compound (0.194 g). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.35 (s, 1H), 7.91 (d, 2H), 7.71 (d, 2H), 7.14 (d, 1H), 7.08 (d, 2H), 6.91 (dd, 1H), 4.38 (dd, 1H), 3.88 (s, 3H), 2.38 – 2.27 (m, 1H), 2.26 – 2.07 (m, 2H), 2.02 – 1.90 (m, 1H). LCMS: m/z 395.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 1. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 2. N-(5-(3,4-Difluorophenoxy)-2-(1,3,4-oxadiazol-2-yl)phenyl)-1 - methyl-5-oxopyrrolidine-2-carboxamide (Compound 224) To a solution of 5-(3,4-difluorophenoxy)-2-(1,3,4-oxadiazol-2-yl)aniline (0.122 g, 1 eq., 422 µmol) in acetonitrile (3 mL) was added 1-methyl-5-oxopyrrolidine-2- carboxylic acid (72.5 mg, 1.2 eq., 506 µmol) and DIPEA (218 mg, 294 µL, 4 eq., 1.69 mmol). HATU (321 mg, 2 eq., 844 µmol) was then added and the mixture was stirred overnight at RT. N-(Chloro(dimethylamino)methylene)-N-methylmethanaminium hexafluorophosphate(V) (237 mg, 2 eq., 844 µmol) and 1-methyl-1H-imidazole (208 mg, 202 µL, 6 eq., 2.53 mmol) were added and the mixture was stirred overnight. The mixture was concentrated in vacuum, diluted with EtOAc (10 mL), washed with NaHSO ₄ (2 mL, 10 %), K ₂ CO ₃ (2 mL, 10 %) and water (2 mL) followed by drying over Na ₂ SO ₄ . EtOAc was evaporated. The residue was purified by HPLC (2-10 min 0-55 % of MeCN, flow rate: 30 mL/min) to afford the title compound (0.0242 g, 58.4 µmol, 13.8 %, 100 % purity). ¹ H NMR (600 MHz, DMSO-d6) δ: 10.89 (s, 1H), 9.38 (s, 1H), 8.01 – 7.89 (m, 2H), 7.57 – 7.50 (m, 1H), 7.45 – 7.38 (m, 1H), 7.04 (dd, J = 8.0, 4.8 Hz, 1H), 6.96 (dd, J = 8.8, 2.5 Hz, 1H), 4.26 (dd, J = 9.1, 3.9 Hz, 1H), 2.70 (s, 3H), 2.38 – 2.21 (m, 3H), 2.01 – 1.93 (m, 1H). LCMS: m/z 415.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for compound 224. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 3. (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1,3- dimethyl-2-oxoimidazolidine-4-carboxamide (Compound 226) 2-Methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (0.07 g, 1 eq., 0.25 mmol), (S)-1,3-dimethyl-2-oxoimidazolidine-4-carboxylic acid (39 mg, 1 eq., 0.25 mmol) and triethylamine hydrochloride (34 mg, 1 eq., 0.25 mmol) were dissolved in DMF (3 mL) followed by stirring for 10 min. Then 1-methyl-1H-imidazole (0.1 g, 99 µL, 5 eq., 1.2 mmol) was added followed by stirring for 10 min. N-(Chloro(dimethyl- amino)methylene)-N-methylmethanaminium hexafluorophosphate(V) (76 mg, 1.1 eq., 0.27 mmol) was then added in a single portion followed by stirring at 20 °C for 10 h. The mixture was filtered and the filtrate was purified by HPLC (Method A) to give the title compound (0.0314 g, 74.2 µmol, 30 %, 100 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.57 (s, 1H), 7.88 (t, 1H), 7.71 (d, 2H), 7.15 (d, 1H), 7.08 (d, 2H), 7.00 – 6.88 (m, 1H), 4.40 – 4.26 (m, 1H), 3.88 (s, 3H), 3.54 (t, 1H), 3.26 – 3.16 (m, 1H), 2.64 (d, 6H). LCMS: m/z 424.2 [M+H] ⁺ . The following compounds were prepared according to the procedure described for compound 226. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 4.4-Hydroxy-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)pheny l)- 1-methyl-5-oxopyrrolidine-3-carboxamide (Compound 228) 2-Methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (100 mg, 1 eq., 353 µmol), 4- acetoxy-1-methyl-5-oxopyrrolidine-3-carboxylic acid (92.3 mg, 1.3 eq., 459 µmol) and 1-methyl-1H-imidazole (174 mg, 169 µL, 6 eq., 2.12 mmol) were dissolved in acetonitrile (2 mL) followed by stirring the mixture at 22 °C for 10 min. Then N- (chloro(dimethylamino)methylene)-N-methylmethanaminium hexafluorophosphate(V) (198 mg, 2 eq., 706 µmol) was added. The mixture was stirred at 22 °C for 16 h.4- Acetoxy-1-methyl-5-oxopyrrolidine-3-carboxylic acid (92.3 mg, 1.3 eq., 459 µmol) and N-(chloro(dimethylamino)methylene)-N-methylmethanaminium hexafluoro- phosphate(V) (198 mg, 2 eq., 706 µmol) were added to the mixture followed by stirring at 22 °C for 16 h. The mixture was concentrated and ammonia (60.1 mg, 10 eq., 3.53 mmol) in methanol solution was added. The reaction mass was stirred at 22 °C for 16 h. The solution was purified by reverse phase HPLC (purification method A) to afford the title compound (5 mg, 0.01 mmol, 3 %, 95 % purity). ¹ H NMR (400 MHz, Methanol- d4) δ: 8.03 – 8.00 (m, 1H), 7.65 – 7.57 (m, 2H), 7.10 – 7.03 (m, 3H), 6.85 (m, 1H), 4.54 (dd, 1H), 3.93 (d, 3H), 3.77 – 3.67 (m, 1H), 3.58 – 3.47 (m, 2H), 3.31 – 3.25 (m, 1H), 2.88 (s, 3H). LCMS: m/z 425.1 [M+H] ⁺ . Example 5. N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo-1-( 5- oxopyrrolidine-2-carbonyl)pyrrolidine-2-carboxamide (Compound 229) To a solution of N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo- pyrrolidine-2-carboxamide (0.047 g, 1 eq., 0.12 mmol) in DMF (2 mL) was added 5- oxopyrrolidine-2-carboxylic acid (15 mg, 1 eq., 0.12 mmol) and diisopropylethylamine (46 mg, 62 µL, 3 eq., 0.36 mmol).The mixture was stirred at RT for 15 minutes and HATU (68 mg, 1.5 eq., 0.18 mmol) was added in a single portion. The resulting solution was stirred at RT for 10 h. The mixture was concentrated in vacuum, diluted with ethylacetate (10 mL), washed with NaHSO ₄ (2 mL, 10 %), K ₂ CO ₃ (2 mL, 10 %) and water (2 mL) followed by drying over Na ₂ SO ₄ . Ethyl acetate was evaporated and the residue was purified by method A to afford the title compound (0.0117 g). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.78 (s, 1H), 7.87 (d, 1H), 7.77 (s, 1H), 7.69 (d, 2H), 7.14 (d, 1H), 7.06 (d, 2H), 6.90 (dd, 1H), 5.16 – 5.07 (m, 1H), 5.07 – 5.00 (m, 1H), 3.90 (s, 3H), 2.70 – 2.56 (m, 1H), 2.46 – 2.30 (m, 3H), 2.05 – 1.89 (m, 4H). LCMS: m/z 506.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 229. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 6.1-Methyl-5-oxo-N-(7-(3-(trifluoromethyl)phenoxy)-2,3-dihyd ro- benzo[b][1,4]dioxin-5-yl)pyrrolidine-2-carboxamide (Compound 233) To a mixture of 5-bromo-7-(3-(trifluoromethyl)phenoxy)-2,3-dihydrobenzo[b]- [1,4]dioxine (217.2 mg, 1 eq., 579.0 µmol), 1-methyl-5-oxopyrrolidine-2-carboxamide (123.5 mg, 1.5 eq., 868.5 µmol) and cesium carbonate (565.9 mg, 3 eq., 1.737 mmol) in toluene (4 mL) under argon Pd ₂ (dba) ₃ (26.51 mg, 0.05 eq., 28.95 µmol) and 4,5-bis(di- phenylphosphino)-9,9-dimethylxanthene (50.25 mg, 0.15 eq., 86.85 µmol) were added and the mixture was heated at 110 °C for 18 h. After cooling to RT the mixture was concentrated and the residue was purified by method A to afford the title compound (0.0286 g). ¹ H NMR (600 MHz, DMSO-d6) δ: 9.68 (s, 1H), 7.59 – 7.54 (m, 1H), 7.42 (d, 1H), 7.39 (d, 1H), 7.25 – 7.19 (m, 2H), 6.47 (d, 1H), 4.44 (dd, 1H), 4.35 – 4.27 (m, 4H), 2.61 (s, 3H), 2.27 – 2.12 (m, 3H), 1.89 – 1.82 (m, 1H). LCMS: m/z 437.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 233. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 7. N-(5-(((3-Fluorophenyl)amino)methyl)-2-methoxyphenyl)-5- oxopyrrolidine-2-carboxamide (Compound 246) Chlorotrimethylsilane (210 mg, 245 µL, 5 eq., 1.93 mmol) was added slowly to methanol (5 mL) at 0 °C and the mixture was stirred at 0 °C for 30 min. To the obtained solution tert-butyl (3-fluorophenyl)(4-methoxy-3-(5-oxopyrrolidine-2-carboxamido )- benzyl)carbamate (300 mg, 58.89 %, 1 eq., 386 µmol) was added and the mixture was stirred at RT for 18 h. The mixture was treated with aqueous NaHCO ₃ solution (10 mL) and extracted with ethyl acetate (2×20 mL). Combined organic phases were washed with brine (2×15 mL), dried over sodium sulfate, filtered, concentrated and the residue was purified by reverse phase HPLC (water-acetonitrile) to afford the title compound (0.0201 g). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.17 (s, 1H), 8.04 – 7.90 (m, 2H), 7.12 – 6.96 (m, 3H), 6.58 – 6.49 (m, 1H), 6.39 (dd, 1H), 6.32 – 6.18 (m, 2H), 4.34 (dd, 1H), 4.16 (d, 2H), 3.82 (s, 3H), 2.38 – 2.28 (m, 1H), 2.28 – 2.02 (m, 2H), 2.03 – 1.85 (m, 1H). LCMS: m/z 358.2 [M+H] ⁺ . Example 8. N-(5-((4,4-Difluorocyclohexyl)oxy)-2-methoxyphenyl)-1-methyl -5- oxopyrrolidine-2-carboxamide (Compound 247) N-(5-hydroxy-2-methoxyphenyl)-1-methyl-5-oxopyrrolidine-2-ca rboxamide (0.0667 g, 1 eq., 252 µmol), triphenylphosphine (86.1 mg, 1.3 eq., 328 µmol) and DEAD (54.9 mg, 49.5 µL, 1.25 eq., 315 µmol) were dissolved in THF (5.5 mL). The mixture was stirred at RT for 30 min.4,4-Difluorocyclohexan-1-ol (48.1 mg, 1.4 eq., 353 µmol) was added to the mixture at RT and stirred for 58 h. The mixture was purified by column chromatography to give the title compound (0.0032 g, 7.9 µmol, 3.1 %, 95 % purity). Purification method C. ¹ H NMR (400 MHz, Methanol-d4) δ: 7.75 (d, 1H), 6.97 (d, 1H), 6.77 (dd, 1H), 4.48 – 4.40 (m, 2H), 3.87 (s, 3H), 2.85 (s, 3H), 2.59 – 2.47 (m, 1H), 2.47 – 2.34 (m, 2H), 2.19 – 2.04 (m, 3H), 1.99 – 1.84 (m, 6H). LCMS: m/z 383.2 [M+H] ⁺ . Example 9. N-(5-((3,4-Difluorobenzyl)oxy)-2,3-dihydrobenzofuran-7-yl)-1 - methyl-5-oxopyrrolidine-2-carboxamide (Compound 248) 7-Bromo-5-((3,4-difluorobenzyl)oxy)-2,3-dihydrobenzofuran (0.100 g, 1 eq., 293 µmol), 1-methyl-5-oxopyrrolidine-2-carboxamide (50.0 mg, 1.2 eq., 352 µmol), cesium carbonate (95.5 mg, 1 eq., 293 µmol), copper (I) iodide (16.7 mg, 0.3 eq., 87.9 µmol) and N1,N2-dimethylcyclohexane-1,2-diamine (25.0 mg, 0.6 eq., 176 µmol) were mixed in N,N-dimethylformamide (2 mL). The mixture was heated at 100 °C under argon atmosphere for 12 h. Then N,N-dimethylformamide was evaporated and the residue was diluted with EtOAc (10 mL), washed with water (2×2 mL), dried over Na ₂ SO ₄ and concentrated in vacuum. A sample of reaction mixture was analyzed by LCMS. Residue was purified by method A to afford the title compound (0.0035 g). ¹ H NMR (400 MHz, Acetonitrile-d ₃ ) δ: 8.03 (s, 1H), 7.59 (d, 1H), 7.46 – 7.36 (m, 1H), 7.36 – 7.24 (m, 2H), 6.74 (d, 1H), 5.01 (s, 2H), 4.61 (t, 2H), 4.23 (dd, 1H), 3.24 (t, 2H), 2.78 (s, 3H), 2.45 – 2.24 (m, 3H). LCMS: m/z 403.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 248. The compound number, structure, starting materials, purification method and characterization data are indicated in the table.

Example 10. N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxotetr a- hydropyrrolo[2,1-b]thiazole-7a(5H)-carboxamide 1,1-dioxide (Compound 252) N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxotetr ahydropyrrolo- [2,1-b]thiazole-7a(5H)-carboxamide (100 mg, 1 eq., 221 µmol) was dissolved in acetic acid (3 mL) and potassium permanganate (55.9 mg, eq., 354 µmol) was added at RT. The mixture was stirred at RT for 24 h. The mixture was poured into sodium hydro- carbonate saturated solution (30 mL) followed by extraction with ethyl acetate (3×30 mL). Combined organic phases were washed with brine (2×30 mL), dried over sodium sulfate, filtered, concentrated and the residue was purified by purification method A to afford the title compound (0.0079 g). ¹ H NMR (400 MHz, Acetonitrile-d ₃ ) δ: 8.77 (s, 1H), 7.99 (d, 1H), 7.70 (d, 2H), 7.15 – 7.05 (m, 3H), 6.96 (dd, 1H), 4.52 – 4.38 (m, 1H), 3.95 (s, 3H), 3.73 – 3.64 (m, 1H), 3.45 – 3.26 (m, 2H), 2.87 – 2.66 (m, 3H), 2.57 – 2.42 (m, 1H). LCMS: m/z 485.2 [M+H] ⁺ . Example 11. N-(3-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxopyrr o- lidine-2-carboxamide (Compound 253) To a solution of 5-oxopyrrolidine-2-carboxylic acid (51.1 mg, 0.40 mmol), 3- methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (112 mg, 0.40 mmol), HATU (226 mg, 0.60 mmol) and dry DMF (2 ml) was added DIPEA (0.34 ml, 2.0 mmol). The mixture was stirred at RT overnight. The reaction mixture was quenched with water (10 ml) followed by extraction with ethyl acetate (2 x 10 ml). The combined organic layers were washed with water, dried, evaporated and then purified by reverse phase chromato- graphy to yield 0.074 g the title compound. ¹ H NMR (600 MHz, DMSO-d6) δ: 1.93 - 2.00 (m, 1 H), 2.08 - 2.22 (m, 2 H), 2.28 - 2.36 (m, 1 H), 3.75 (s, 3 H), 4.14 (dd, 1 H), 6.48 (t, 1 H), 6.97 (t, 1 H), 7.15 - 7.21 (m, 3 H), 7.76 (d, 2 H), 7.86 (s, 1 H), 10.14 (s, 1 H). LCMS: m/z 395.2 [M+H] ⁺ The following compounds were prepared according to the procedure described for Compound 253. The compound number, structure, starting materials, purification method and characterization data are indicated in the table.

Example 12. (R)-N-(2-methoxy-5-(4-(trifluoromethoxy)phenoxy)phenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 290) To a mixture of 2-methoxy-5-(4-(trifluoromethoxy)phenoxy)aniline (0.060 g, 0.20 mmol), (2R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid (0.029 g, 0.20 mmol) and HATU (0.114 g, 0.30 mmol) in dry DMF (1.0 ml) was added DIPEA (0.174 ml, 1.00 mmol). The mixture was stirred overnight at RT. The mixture was diluted with EtOAc and washed with water and brine. Organic phase was dried and evaporated. The crude product was purified by reverse phase flash chromatography to afford 0.056 g of the of the title compound. ¹ H NMR (400 MHz, CDCl3) δ: 8.17 (d, 1H), 8.07 (s, 1H), 7.11-7.18 (m, 2H), 6.91-6.98 (m, 2H), 6.87 (d, 1H), 6.77 (dd, 1H), 4.07-4.14 (m, 1H), 3.90 (s, 3H), 2.94 (s, 3H), 2.37-2.63 (m, 3H), 2.10-2.20 (m, 1H). LCMS: m/z 425.0 [M+H] ⁺ The following compounds were prepared according to the procedure described for Compound 290. The compound number, structure, starting materials, purification method and characterization data are indicated in the table.

Example 13. N-(2-Fluoro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-1-methyl- 5- oxopyrrolidine-2-carboxamide (Compound 328) To a mixture of 2-fluoro-5-(4-(trifluoromethoxy)phenoxy)aniline (0.069 g, 0.24 mmol), 1-methyl-5-oxopyrrolidine-2-carboxylic acid (0.034 g, 0.24 mmol) and 1- methylimidazole (0.071 ml, 0.89 mmol) in dry acetonitrile (1.0 ml) was added N,N,N‘,N‘-tetramethylchloroformamidinium-hexafluorophosp hate (0.081 g, 0.288 mmol). The mixture was stirred overnight at RT. The mixture was diluted with EtOAc and washed with water and brine. Organic phase was dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford 0.028 g of the title compound. ¹ H NMR (400 MHz, CDCl3) δ: 8.05 (dd, 1H), 7.81 (s, 1H), 7.14-7.23 (m, 2H), 7.05-7.14 (m, 1H), 6.92-7.03 (m, 2H), 6.71-6.80 (m, 1H), 4.10-4.19 (m, 1H), 2.93 (s, 3H), 2.37-2.64 (m, 3H), 2.10-2.21 (m, 1H). LCMS: m/z 413.0 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 328. The compound number, structure, starting materials and characterization data are indicated in the table. Example 14. N-(2-Methoxy-5-((4-(trifluoromethyl)-pyridin-2-yl)oxy)phenyl )-1- (2-methoxyacetyl)-5-oxopyrrolidine-2-carboxamide (Compound 331)

To a mixture of 2-methoxy-5-((4-(trifluoromethyl)pyridin-2-yl)oxy)aniline (0.071 g, 0.25 mmol), 1-(2-methoxyacetyl)-5-oxopyrrolidine-2-carboxylic acid (0.053 g, 0.25 mmol) in EtOAc (0.30 ml) and pyridine (0.15 ml) was added 1- propanephosphonic acid cyclic anhydride, 50 wt-% in EtOAc (0.25 ml, 0.424 mmol). The mixture was stirred at RT overnight. Reaction was quenched with 0.5 % HCl- solution and diluted with water and EtOAc. Phases were separated and organic phase was washed with 0.5 % HCl-solution, water and brine, dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.046 g. ¹ H NMR (400 MHz, CDCl3) δ: 8.45 (s, 1H), 8.30 (d, 1H), 8.20 (s, 1H), 7.04-7.22 (m, 2H), 6.82-7.00 (m, 2H), 4.88 (d, 1H), 4.52-4.74 (m, 2H), 3.93 (s, 3H), 3.47 (s, 3H), 2.84-3.03 (m, 1H), 2.47-2.64 (m, 1H), 2.22-2.47 (m, 2H). LCMS: m/z 468.5 [M+H] ⁺ The following compounds were prepared according to the procedure described for Compound 331. The compound number, structure, starting materials and characterization data are indicated in the table. Example 15. N-(2-Bromo-5-(3-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 366) To a cooled (0-5 C) mixture of 1-methyl-5-oxopyrrolidine-2-carboxylic acid (0.067 g, 0.468 mmol) in dry DCM (1.5 ml) was added 1-chloro-N,N,2-trimethyl-1- propenylamine (0.065 ml, 0.488 mmol) and the mixture was stirred at 0-5 ºC for 1 h. Then 2-bromo-5-(3-(trifluoromethyl)phenoxy)aniline (0.18 g, 0.390 mmol) dissolved in dry DMF (0.5 ml) and DIPEA (0.34 ml, 1.951 mmol) were added and the mixture was stirred at RT overnight. DCM was evaporated and the mixture diluted with EtOAc. Organic phase was washed with water and brine, dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.019 g. ¹ H NMR (600 MHZ, d6-DMSO) δ: 9.88 (s, 1H), 7.72 (d, 1H), 7.65 (t, 1H), 7.51-7.55 (m, 1H), 7.42 (d, 1H), 7.36-7.39 (m, 1H), 7.34 (dd, 1H), 6.93 (dd, 1H), 4.31- 4.38 (m, 1H), 2.70 (s, 3H), 2.17-2.35 (m, 3H), 1.94-2.02 (m, 1H). LCMS: m/z 457.1 [M+H] ⁺ . Example 16. N-(2-Cyano-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 367) The compound was prepared according to the procedure of the preceding Example starting from 1-methyl-5-oxopyrrolidine-2-carboxylic acid (0.051 g, 0.359 mmol), DCM (1.5 ml), 1-chloro-N,N,2-trimethyl-1-propenylamine (0.057 ml, 0.431 mmol), 2-amino-4-(4-(trifluoromethyl)phenoxy)benzonitrile (0.10 g, 0.359 mmol) and DMF (0.75 ml). Yield: 0.022 g. ¹ H NMR (600 MHz, d ₆ -DMSO) δ: 10.5 (s, 1H), 7.90 (d, 1H), 7.81-7.86 (m, 2H), 7-31-7.37 (m, 2H), 7.30 (d, 1H), 7.08 (dd, 1H), 4.30 (dd, 1H), 2.70 (s, 3H), 2.19-2.36 (m, 3H), 1.94-2.01 (m, 1H). LCMS: m/z 404.4 [M+H] ⁺ . Example 17. N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 368) The compound was prepared using the procedure of Intermediate 306 staring from N-(2-fluoro-5-hydroxyphenyl)-1-methyl-5-oxopyrrolidine-2-car boxamide (0.071 g, 0.28 mmol), 2-chloro-5-(trifluoromethyl)pyridine (0.051 g, 0.28 mmol) and K ₂ CO ₃ (0.058 g, 0.42 mmol) in dry DMF (1.0 ml). Crude was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.078 g. ¹ H NMR (600 MHz, CDCl3) δ: 8.40-8.43 (m, 1H), 8.21 (dd, 1H), 7.92 (dd, 1H), 7.79 (s, 1H), 7.18 (dd, 1H), 7.05 (d, 1H), 6.91 (dq, 1H), 4.158dd, 1H), 2.93 (s, 3H), 2.54-2.62 (m, 1H), 2.39-2.53 (m, 2H), 2.11-2.18 (m, 1H). LCMS: m/z 398.6 [M+H] ⁺ . Example 18. N-(2-Fluoro-5-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)- 1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 369) The compound was prepared using the procedure of Intermediate 339 staring from N-(2-fluoro-5-hydroxyphenyl)-1-methyl-5-oxopyrrolidine-2-car boxamide (0.071 g, 0.28 mmol), 2-chloro-5-(trifluoromethyl)pyridine (0.051 g, 0.28 mmol) and K ₂ CO ₃ (0.058 g, 0.42 mmol) in dry DMF (1.0 ml). Crude was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.078 g. ¹ H NMR (600 MHz, CDCl ₃ ): δ 8.40-8.43 (m, 1H), 8.21 (dd, 1H), 7.92 (dd, 1H), 7.79 (s, 1H), 7.18 (dd, 1H), 7.05 (d, 1H), 6.91 (dq, 1H), 4.158dd, 1H), 2.93 (s, 3H), 2.54-2.62 (m, 1H), 2.39-2.53 (m, 2H), 2.11-2.18 (m, 1H). LCMS: m/z 398.6 [M+H] ⁺ . Example 19. (2S,4R)-4-Hydroxy-N-(2-methoxy-5-(4- (trifluoromethyl)phenoxy)phenyl)pyrrolidine-2-carboxamide (Compound 370) To a mixture of palladium (10 wt-% on carbon, 0.045 g, 0.042 mmol) in methanol (15 ml) was added benzyl (2S,4R)-4-hydroxy-2-((2-methoxy-5-(4-(trifluoro- methyl)phenoxy)phenyl)carbamoyl)pyrrolidine-1-carboxylate (0.111 g, 0.209 mmol) dissolved in methanol (2.0 ml). The mixture was stirred vigorously while ammonium formate (0.132 mg, 2.09 mmol) was added. Stirring was continued at 50 ºC until reaction was completed. Cooled mixture was filtered through a short plug of Celite. Celite was washed with methanol. Filtrate was evaporated and re-dissolved in EtOAc. Organic phase was washed with water and brine, dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.041 g. ¹ H NMR (600 MHz, d ₆ -DMSO) δ: 10.3 (s, 1H), 8.13 (d, 1H), 7.68-7.73 (m, 2H), 7.13 (d, 1H), 7.05-7.10 (m, 2H), 6.85 (dd, 1H), 4.71 (d, 1H), 4.16-4.20 (m, 1H), 3.89 (s, 3H), 3.87-3.93 (m, 1H), 3.48 (bs, 1H), 2.88 (d, 1H), 2.74 (d, 1H), 1.99-2.06 (m, 1H), 1.72-1.79 (m, 1H). LCMS: m/z 397.6 [M+H] ⁺ . Example 20. (S)-1-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)- phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 371) To a cooled (0-5 ºC) solution of (S)-N-(2-methoxy-5-(4-(trifluoromethyl)- phenoxy)phenyl)-5-oxopyrrolidine-2-carboxamide (0.086 g, 0.225 mmol) in dry DCM (2.0 ml) was added acetyl chloride (0.018 ml, 0.248 mmol) dissolved in dry DCM (0.25 ml) and triethylamine (0.039 ml, 0.281 mmol) and the mixture was stirred overnight at RT. More acetyl chloride (0.018 ml, 0.248 mmol) and triethylamine (0.039 ml, 0.281 mmol) were added and stirring continued until the reaction was completed. The mixture was diluted with DCM and washed with water, saturated NaHCO ₃ -solution and brine, dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.072 g. ¹ H NMR (400 MHz, CDCl ₃ ) δ: 9.44 (s, 1H), 8.18 (s, 1H), 7.43-7.60 (m, 2H), 6.91-7.07 (m, 2H), 6.86 (d, 1H), 6.74 (d, 1H), 4.75 (d, 1H), 3.91 (s, 3H), 3.59 (t, 1H), 3.47 (dd, 1H), 2.41-2.55 (m, 1H), 2.15 (s, 3H), 1.81-2.22. (m, 3H). LCMS: m/z 423.6 [M+H] ⁺ . Example 21. N-(2-Hydroxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 5- oxopyrrolidine-2-carboxamide (Compound 372) To a solution of Compound 48 (100 mg, 245 µmol) in DCM (5 ml) was added tetrabutyl ammonium iodide (90 mg, 245 µmol) at RT. The solution was cooled to -50 °C. Then BCl31 M in heptane (1.469 ml, 1469 µmol) was added dropwise. The mixture was stirred for 10 min at -78 °C and then 1 h 20 min at RT. The mixture was diluted with DCM (10 ml) and poured into ice cold 1 N HCl (5 ml). Phases were separated. The aqueous phase was extracted twice with DCM. The combined organic phases were concentrated under reduced pressure. The crude product was purified by column chromatography to afford the title compound (0.055 g). ¹ H NMR (400MHz, DMSO) δ: 10.06 (br s 1H), 9.57 (s, 1H), 7.79 (d, 1H), 7.69 (d, 2H), 7.05 (d, 2H), 6.94 (d, 1H), 6.80-6.75 (m, 1H), 4.50-4.42 (m, 1H), 2.65 (s, 3H), 2.31-2.12 (m, 3H), 1.95-1.84 (m, 1H). LCMS: m/z 395.4 [M+H] ⁺ The following compound was prepared according to the procedure described for Compound 372. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 22. N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-1-methyl- 6- oxopiperazine-2-carboxamide (Compound 374) tert-Butyl 3-((2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)carbamoyl )-4- methyl-5-oxopiperazine-1-carboxylate (30.6 mg, 58.5 µmol) was dissolved in HCl (dioxane solution) (2.13 g, 1.43 mL, 10 w-%, 5.85 mmol) and stirred at RT overnight. The mixture was purified by HPLC (Method D) to afford 12.9 mg of the title compound (12.9 mg, 30.5 µmol, 52.1 %, 100 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.93 (s, 1H), 7.92 (d, 1H), 7.71 (d, 2H), 7.10 (dd, 3H), 6.91 (dd, 1H), 4.20 (s, 1H), 3.88 (d, 3H), 3.26 (s, 2H), 3.13 (s, 2H), 2.77 (s, 3H). LCMS: m/z 424.2 [M+H] ⁺ . The following compounds were prepared according to the procedure described for Compound 374. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 23.1-Methyl-6-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-dihy dro- benzofuran-7-yl)piperazine-2-carboxamide (Compound 376) Tert-butyl 4-methyl-3-oxo-5-((5-(4-(trifluoromethyl)phenoxy)-2,3-dihydr o- benzofuran-7-yl)carbamoyl)piperazine-1-carboxylate (0.0416 g, 1 eq., 77.7 µmol) was dissolved in methanol (3 mL). TMS-Cl (42.2 mg, 49.3 µL, 5 eq., 388 µmol) was added dropwise. The mixture was stirred at 25 °C for 16 h and then concentrated under reduced pressure. The obtained mixture was subjected to HPLC (purification method D) to give the title compound (0.01 g, 0.02 mmol, 30 %, 95 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 7.70 (d, 2H), 7.60 (s, 1H), 7.07 (d, 2H), 6.86 (s, 1H), 4.65 (t, 2H), 4.20 (t, 1H), 3.29 – 3.20 (m, 4H), 3.18 – 3.02 (m, 2H), 2.74 (s, 3H). LCMS: m/z 436.2 [M+H] ⁺ . Example 24. (R)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-oxo - 1-(1H-pyrazol-4-yl)pyrrolidine-2-carboxamide (Compound 377) TFA (335 mg, 226 µL, 50 eq., 2.94 mmol) was added to (R)-N-(2-methoxy-5- (4-(trifluoromethyl)phenoxy)phenyl)-1-(1-(4-methoxybenzyl)-1 H-pyrazol-4-yl)-5- oxopyrrolidine-2-carboxamide (0.0341 g, 1 eq., 58.7 µmol) followed by refluxing the mixture for 16 h. Then the solvent was evaporated and the residue was purified by HPLC (Method G) to give the title compound (0.0057 g, 12 µmol, 21 %, 100 % purity). 1H NMR (400 MHz, Acetonitrile-d3) δ: 8.62 (s, 1H), 8.01 (d, 1H), 7.79 (s, 2H), 7.66 (d, 2H), 7.07 (dd, 3H), 6.88 (dd, 1H), 4.75 (dd, 1H), 3.92 (s, 3H), 2.66 – 2.36 (m, 4H), 2.23 – 2.13 (m, 2H). LCMS: m/z 459.1 [M-H]-. The following compounds were prepared according to the procedure described for Compound 377. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 25.1-(3-Amino-3-oxopropyl)-N-(2-methoxy-5-(4-(trifluoromethy l)- phenoxy)phenyl)-5-oxopyrrolidine-2-carboxamide (Compound 379) To a solution of 1-(2-cyanoethyl)-N-(2-methoxy-5-(4- (trifluoromethyl)phenoxy)phenyl)-5-oxopyrrolidine-2-carboxam ide (158 mg, 1 eq., 353 µmol) in DMSO (2 mL) potassium carbonate (97.6 mg, 2 eq., 706 µmol) followed by hydrogen peroxide (343 mg, 309 µL, 35 w-%, 10 eq., 3.53 mmol) was added. The mixture was stirred at 40 °C for 36 h. Water (20 mL) was added to the residue and the resulted mixture was extracted with ethyl acetate (2×20 mL). Organic layers were combined, washed with brine (20 mL), dried over sodium sulfate, filtered and concentrated. The residue was purified by reverse phase HPLC (purification method B) to afford the title compound (13.4 mg, 28.8 µmol, 8.15 %, 100 % purity) ¹ H NMR (400 MHz, DMSO-d6) δ: 9.64 (s, 1H), 7.89 (s, 1H), 7.70 (d, 2H), 7.36 (s, 1H), 7.19 – 7.05 (m, 3H), 6.92 (d, 1H), 6.82 (s, 1H), 4.63 – 4.55 (m, 1H), 3.88 (s, 3H), 3.64 – 3.51 (m, 1H), 3.20 – 2.96 (m, 2H), 2.31 – 2.12 (m, 4H), 1.96 – 1.85 (m, 1H). LCMS: m/z 466.2 [M+H] ⁺ . Example 26. (2S,4S)-4-Hydroxy-N-(2-methoxy-5-(4- (trifluoromethyl)phenoxy)phenyl)-1-methyl-5-oxopyrrolidine-2 -carboxamide (Compound 380) (2S,4S)-4-((tert-Butyldimethylsilyl)oxy)-N-(2-methoxy-5-(4-( trifluoromethyl)- phenoxy)phenyl)-1-methyl-5-oxopyrrolidine-2-carboxamide (0.185 g, 1 eq., 343 µmol) was dissolved in THF (2 mL). Then TBAF (89.8 mg, 343 µL, 1 molar, 1 eq., 343 µmol) was added to the mixture dropwise at 0 °C. The resulting mixture was stirred for 20 min and slowly heated to 20 °C, stirred at this temperature for 10 h and purified by HPLC (purification method A) to give the title compound (0.0374 g, 88.1 µmol, 25.7 %, 100 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.68 (s, 1H), 7.87 (s, 1H), 7.71 (d, 2H), 7.14 (d, 1H), 7.08 (d, 2H), 6.96 – 6.88 (m, 1H), 4.31 (t, 1H), 4.12 (t, 1H), 3.88 (s, 3H), 2.67 (s, 3H), 2.65 – 2.57 (m, 1H), 1.74 – 1.57 (m, 1H). LCMS: m/z 425.0 [M+H] ⁺ . Example 27.1-Imino-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl )- hexahydro-1λ ⁶ -thiopyran-4-carboxamide 1-oxide (Compound 381) A mixture of N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)tetrahydro - 2H-thiopyran-4-carboxamide 1-oxide (250 mg, 1 eq., 585 µmol), phenyl- λ ³ -iodanediyl diacetate (565 mg, 3 eq., 1.75 mmol) and carbamic acid, ammonia salt (183 mg, 4 eq., 2.34 mmol) in methanol (12 mL) was stirred at 22 °C for 12 h. The mixture was concentrated to provide a mixture of a light yellow sludge and an immiscible colorless liquid. The mixture was washed twice with hexane (2×10 mL) by decantation and dried under vacuum. The residue was triturated and stirred in ethyl acetate, filtered, and the collected solid was washed with additional ethyl acetate. The filtrate was concentrated to provide a mixture of cis and trans isomers and purified by HPLC (purification method A) to give the title compound (30.5 mg, 65 µmol, 11 %, 95 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.34 (d, 1H), 7.87 (t, 1H), 7.70 (d, 2H), 7.09 (dd, 3H), 6.88 (dd, 1H), 3.87 (s, 3H), 3.70 (s, 0H), 3.48 (s, 1H), 3.16 – 2.79 (m, 4H), 2.16 – 1.92 (m, 4H). LCMS: m/z 443.1 [M+H] ⁺ . Example 28. N-(4-Fluoro-2-methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- 3- methyl-2-oxoimidazolidine-4-carboxamide (Compound 382) N-(5-(2-Chloro-4-(trifluoromethyl)phenoxy)-4-fluoro-2-methox yphenyl)-3- methyl-2-oxoimidazolidine-4-carboxamide (0.032 g, 1 eq., 69 µmol) was dissolved in methanol (5 mL). Formic acid, ammonia salt (26 mg, 6 eq., 0.42 mmol) and palladium (7.4 mg, 10 w-%, 0.1 eq., 6.9 µmol) were added. The resulting mixture was stirred at 60 °C for 12 h, cooled to RT and filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in DMSO (2 mL) and to the obtained solution metal scavenger (SiliaMetS Dimercaptotriazine, 50 mg) was added. The mixture was stirred at RT for 3 h and filtered. The clear filtrate was purified by HPLC (purification method B) to give the title compound (0.0038 g, 8.4 µmol, 12 %, 95 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.55 (s, 1H), 7.95 (d, 1H), 7.72 (d, 2H), 7.29 (d, 1H), 7.10 (d, 2H), 6.44 (s, 1H), 4.49 – 4.26 (m, 1H), 3.89 (s, 3H), 3.52 (t, 1H), 3.16 (t, 1H), 2.61 (s, 3H). LCMS: m/z 428.0 [M+H] ⁺ Example 29.1,4-Dimethyl-6-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3- dihydrobenzofuran-7-yl)piperazine-2-carboxamide (Compound 383) To a solution of 1-methyl-6-oxo-N-(5-(4-(trifluoromethyl)phenoxy)-2,3-di- hydrobenzofuran-7-yl)piperazine-2-carboxamide (0.022 g, 1 eq., 51 µmol) in 1,4- dioxane (2 mL) was added NaCNBH4 (6.4 mg, 2 eq., 0.10 mmol) and water solution of formaldehyde (8.2 mg, 7.5 µL, 37 w-%, 2 eq., 0.10 mmol). Thereafter HOAc (0.01 mL) was added and the mixture was stirred at 25 °C for 12 h and evaporated. The residue was dissolved in DMSO (2 mL) and the metal scavenger (SiliaMetS Dimercaptotriazine, 10 mg) was added. The obtained mixture was stirred at RT for 3 h, filtered and the clear solution was purified by HPLC (purification method A) to afford the title compound (0.0052 g, 11 µmol, 22 %, 95 % purity). ¹ H NMR (500 MHz, DMSO-d6) δ: 9.97 (s, 1H), 7.68 (d, 2H), 7.57 (s, 1H), 7.05 (d, 2H), 6.84 (s, 1H), 4.63 (t, 2H), 4.20 (t, 1H), 3.23 (t, 2H), 3.12 (d, 1H), 2.93 (dd, 1H), 2.82 – 2.64 (m, 5H), 2.17 (s, 3H). LCMS: m/z 450.2 [M+H] ⁺ Example 30. N-(5-(4-Amino-2-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 384) N-(5-(2-Fluoro-4-nitrophenoxy)-2-methoxyphenyl)-1-methyl-5-o xopyrrolidine- 2-carboxamide (0.080 g, 1 eq., 0.20 mmol) was dissolved in MeOH and dihydroxy- palladium (28 mg, 10 w-%, 0.1 eq., 20 µmol) was added. The resulting mixture was stirred under hydrogen atmosphere for 16 h, filtered and concentrated to give the title compound (0.065 g, 0.16 mmol, 79 %, 90 % purity). LCMS: m/z 393.0 [M+H] ⁺ Example 31. N-(5-(4-Chloro-2-fluorophenoxy)-2-methoxyphenyl)-1-methyl-5- oxopyrrolidine-2-carboxamide (Compound 385) To a solution of N-(5-(4-amino-2-fluorophenoxy)-2-methoxyphenyl)-1-methyl- 5-oxopyrrolidine-2-carboxamide (0.056 g, 1 eq., 0.15 mmol) in hydrochloric acid, 22 % (0.5 mL) solution of sodium nitrite (12 mg, 1.2 eq., 0.18 mmol) in water (0.1 mL) was added at 0 °C. The resulting mixture was stirred at the same temperature for 15 min, then the mixture was poured into solution of copper(I) chloride (21 mg, 1.4 eq., 0.21 mmol) in 37 % hydrochloric acid (2 mL) at 0 °C. The resulting mixture was stirred at 22 °C for 10 h. The mixture was concentrated under reduced pressure and purified by HPLC (purification method A) to give the title compound (0.0181 g, 46.1 µmol, 31 %, 100 % purity). ¹ H NMR (400 MHz, DMSO-d6) δ: 9.61 (s, 1H), 7.83 (d, 1H), 7.69 – 7.53 (m, 1H), 7.26 (d, 1H), 7.06 (t, 2H), 6.88 – 6.70 (m, 1H), 4.55 – 4.39 (m, 1H), 3.85 (s, 3H), 2.64 (s, 3H), 2.41 – 2.11 (m, 3H), 1.95 – 1.74 (m, 1H). LCMS: m/z 393.0 [M+H] ⁺ . Example 32. N-(5-(3-Acetylphenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrro- lidine-2-carboxamide (Compound 386) a) 1-(4-(4-Methoxy-3-nitrophenoxy)phenyl)ethan-1-one 4-Acetylphenylboronic acid (0.33 g, 1.99 mmol), 4-methoxy-3-nitrophenol (0.28 g, 1.66 mmol), Cu(OAc) ₂ (0.451 mg, 2.48 mmol) and freshly activated powdered 4 Å molecular sieves were added to dry DCM (20 mL). Et ₃ N (1.15 mL, 8.28 mmol) was then added to the mixture. The mixture was stirred under air atmosphere. Reaction progress was monitored by LCMS. After 24 h, the resulting slurry was filtered through celite and concentrated. The crude product was purified by flash column chromato- graphy (heptane: EtOAc) to yield 0.3 g of the title compound. LCMS: m/z 288.21 [M+H] ⁺ . b) 1-(4-(3-Amino-4-methoxyphenoxy)phenyl)ethan-1-one A mixture of 1-(4-(4-methoxy-3-nitrophenoxy)phenyl)ethan-1-one (300 mg, 1.04 mmol), zinc (0.68 g, 10 eq., 10.44 mmol), ammonium chloride (0.56 g, 10 eq. 10.44 mmol) in THF (5 ml), MeOH (3 ml) and water (3 ml) was stirred at RT for 4 h. The mixture was filtered through celite. The filtrate was washed with water (2×30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by flash chromatography to afford (0.19 g) of the title compound. LCMS: m/z 258.65[ M+H] ⁺ . c) N-(5-(4-Acetylphenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrrol idine-2- carboxamide (Compound 386) To a solution of 1-methyl-5-oxopyrrolidine-2-carboxylic acid (22.25 mg, 0.15 mmol), 1-(4-(3-amino-4-methoxyphenoxy)phenyl)ethan-1-one (40 mg, 0.16 mmol) and TEA (0.11, 0.78 mmol) in dry DMF (2 ml) at 0 ^° C, was added 1-propanephosphonic acid cyclic anhydride (0.73 ml, 1.24 mmol). The mixture was stirred at RT overnight. The reaction mixture was quenched with water (10 ml) then extracted with ethyl acetate (2 x10 ml). The combined organic layers were washed with 2 M NaHCO ₃ , then with water, dried over sodium sulfate, evaporated and then purified by reverse phase chromatography to yield (40.5 mg) of the title compound. ¹ H NMR (600 MHz, DMSO- d6): δ: 1.86 - 1.92 (m, 1H), 2.16 - 2.30 (m, 3H), 2.52 - 2.54 (m, 3H), 2.61 - 2.65 (m, 3H), 3.89 (s, 3H), 4.47 (dd, 1H), 6.91 (dd, 1H), 6.98 - 7.01 (m, 2H), 7.14 (d, 1H), 7.87 (d, 1H), 7.94 - 8.02 (m, 2H), 9.65 (s, 1H). LCMS: m/z 383.28 [M+H] ⁺ . Example 33. N-(5-(3-Acetylphenoxy)-2-methoxyphenyl)-1-methyl-5-oxopyrro- lidine-2-carboxamide (Compound 387) a) 1-Methoxy-4-nitro-2-(4-(trifluoromethyl)benzyl)benzene A mixture of 2-methoxy-5-nitro benzaldehyde (0.5 g, 2.8 mmol) and toluene- sulfon hydrazide (0.51 g, 2.8 mmol) in 1,4-dioxane (5 ml) was heated at 60 ^° C for 90 min. To the crude (E)-N'-(2-methoxy-5-nitrobenzylidene)-4-methylbenzenesulfono - hydrazide was added K ₂ CO ₃ (0.53 g, 3.86 mmol) and 4-(trifluoromethyl)phenylboronic acid (0.49 g, 2.6 mmol). The mixture was heated under nitrogen atmosphere at 110 ^° C for 4 h. After cooling at RT the mixture was quenched with 2 M NaHCO ₃ (5 ml). The mixture was extracted with ethyl acetate (2 x 10 ml). The combined organic layers were washed with water, dried, evaporated and then purified by flash chromatography to yield (0.35 g) of the title compound. LCMS: m/z 312.2 [M+H] ⁺ . b) 4-Methoxy-3-(4-(trifluoromethyl)benzyl)aniline A mixture of 1-methoxy-4-nitro-2-(4-(trifluoromethyl)benzyl)benzene (100 mg, 0.32 mmol), zinc (0.21 g, 10 eq., 3.21 mmol) and ammonium chloride (0.17 g, 10 eq. 3.21 mmol) in THF (10 ml), MeOH (3 ml) and water (3 ml) was stirred at RT for 4 h. The mixture was filtered through celite. The filtrate was washed with water (2 × 30 mL), dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by flash chromatography to afford (0.12 g) of the title compound. LCMS: m/z 282.05 [M+H] ⁺ . c) N-(4-Methoxy-3-(4-(trifluoromethyl)benzyl)phenyl)-1-methyl-5 -oxo- pyrrolidine-2-carboxamide (Compound 387) To a solution of 1-methyl-5-oxopyrrolidine-2-carboxylic acid (45.8 mg, 0.32 mmol), 4-methoxy-3-(4-(trifluoromethyl)benzyl)aniline (90 mg, 0.32 mmol) and TEA (0.22, 1.60 mmol) in dry DMF (2 ml) at 0 ^° C was added 1-propanephosphonic acid cyclic anhydride (1.51 ml, 2.56 mmol). The mixture was stirred at RT overnight. The reaction mixture was quenched with water (10 ml) then extracted with ethyl acetate (2 x 10 ml). The combined organic layers were washed with 2 M NaHCO ₃ , then with water, dried over sodium sulfate, evaporated and then purified by reverse phase chromato- graphy to yield (5 mg) of the title compound. ¹ H NMR (400 MHz, Chloroform-d) δ: 1.75 - 2.02 (m, 1H), 2.06 - 2.22 (m, 1H), 2.31 - 2.59 (m, 3H), 2.81 - 2.91 (m, 3H), 3.79 - 3.93 (m, 3H), 3.96 - 4.10 (m, 3H), 6.85 (d, 1H), 7.25 - 7.33 (m, 4H), 7.44 - 7.57 (m, 3H), 7.84 (br s, 1H). LCMS: m/z 282.05 [M+H] ⁺ . Example 34. N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-2-oxo-2,3 - dihydrooxazole-4-carboxamide (Compound 388) TMA (2 M in Chlorobenzene, 397 µL, 0.794 mmol) was added to a mixture of 2-methoxy-5-(4-(trifluoromethyl)phenoxy)aniline (0.075 g, 0.265 mmol) and ethyl-2- oxo-2,3-dihydrooxazole-4-carboxylate (0.064 g, 0.397 mmol) in toluene (2 ml) followed by heating the mixture at 90 ^° C for 3 h. The reaction mixture was quenched with ice cold water. The aqueous layer was extracted with EtOAc (2 x 5 ml). The combined organic layers were evaporated and then purified by reverse phase chromato- graphy to yield 0.029 g of the title compound. ¹ H NMR (400 MHz, DMSO-d ₆ ) δ: 3.87 (3H, s), 7.00 (1H, m), 7.11 (2H, d), 7.17 (1H, d), 7.59 (1H, d), 7.72 (2H, d), 7.98 (1H, s), 9.46 (1H, s), 11.44 (1H, br s). LCMS: m/z 395.2 [M+H] ⁺ Example 35. N-(3-(3,4-Difluorophenoxy)-6-methoxy-2-methylphenyl)-1- methyl-5-oxopyrrolidine-2-carboxamide (Compound 389) To a solution of 1-methyl-5-oxopyrrolidine-2-carboxylic acid (15 mg, 0.10 mmol), 3-(3,4-difluorophenoxy)-6-methoxy-2-methylaniline (24 mg, 0.09 mmol), T ₃ P (50 % in EtOAc, 80 μl, 0.14 mmol) and DCM (2 ml) was added DIPEA (47 μl, 0.27 mmol). After refluxing for 3 h, additional starting material and reagents were added (1- methyl-5-oxopyrrolidine-2-carboxylic acid 1.15 eq., T ₃ P 1.5 eq., DIPEA 3.0 eq.) followed by stirring in a closed vessel at 80 ^° C for 7 h. The reaction mixture was quenched with 2N NaOH (2 ml). The organic layer was separated and the aqueous layer was extracted with EtOAc (1 x 4 ml). The combined organic layers were evaporated and then purified by reverse phase chromatography to yield 0.016 g of the title compound. 1H NMR (400 MHz, DMSO-d ₆ ) δ: 1.94 (3H, s), 1.94 - 2.03 (1H, m), 2.19 - 2.37 (3H, m), 2.71 (3H, s), 3.79 (3H, s), 4.26 - 4.33 (1H, m), 6.61 (1H, m), 6.90 - 7.02 (3H, m), 7.36 - 7.45 (1H, m), 9.66 (1H, s). LCMS: m/z 391.1 [M+H] ⁺ The following compounds were prepared according to the procedure described for Compound 389. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 36. N-(2-Hydroxy-5-(3-methoxy-4-(trifluoromethyl)phenoxy)phenyl) - 1-methyl-5-oxopyrrolidine-2-carboxamide (Compound 410) BCl ₃ (1M in heptane, 798 µL, 0.798 mmol) was added dropwise to a cooled solution of N-(2-methoxy-5-(3-methoxy-4-(trifluoromethyl)phenoxy)phenyl) -1-methyl- 5-oxopyrrolidine-2-carboxamide (0.100 g, 0.228 mmol) in DCM (9 ml) at -50 ^° C followed by stirring at RT for 50 min. The reaction mixture was quenched with 1 N HCl (5 ml). The organic layer was separated and evaporated. The residue was purified by reverse phase chromatography to yield 0.066 g of the title compound. ¹ H NMR (400 MHz, DMSO-d6) δ: 1.85 - 1.95 (1H, m), 2.13 - 2.35 (3H, m), 2.65 (3H, s), 3.84 (3H, s), 4.43 - 4.50 (1H, m), 6.42 (1H, m), 6.78 (1H, m), 6.86 (1H, d), 6.94 (1H, d), 7.53 (1H, d), 7.79 (1H, d), 9.57 (1H, s), 10.07 (1H, s). LCMS: m/z 425.2 [M+H] ⁺ Example 37. N-(5-(2-Hydroxy-4-(trifluoromethyl)phenoxy)-2-methoxyphenyl) - 1-methyl-5-oxopyrrolidine-2-carboxamide (Compound 411) NaH (60 % in oil, 0.028 g, 0.704 mmol) was added to a cooled solution of N-(5- (2-fluoro-4-(trifluoromethyl)phenoxy)-2-methoxyphenyl)-1-met hyl-5-oxopyrrolidine-2- carboxamide (0.100 g, 0.235 mmol) in DMF (2 ml) at 0 ^° C followed by stirring for 15 min at RT. Then 2-(Methylsulfonyl)ethanol was added and the mixture was heated at 50 °C for 2.5 h. Additional NaH (60 % in oil , 5 eq.) and 2-(Methylsulfonyl)ethanol were then added twice and heated at 80 ^° C for 5 h and at 100 ^° C for 5.5 h, respectively. The reaction mixture was quenched with 2 N HCl (2 ml) and extracted with EtOAc (3 x 3 ml). The organic layer was separated and evaporated. The residue was purified by reverse phase chromatography to yield 0.012 g of the title compound. ¹ H NMR (600 MHz, DMSO-d ₆ ) δ: 1.85 - 1.92 (1H, m), 2.16 - 2.31 (3H, m), 2.64 (3H, s), 3.85 (3H, s), 4.46 (1H, m), 6.76 (1H, m), 6.92 (1H, d), 7.07 (1H, d), 7.11 (1H, m), 7.20 (1H, d), 7.80 (1H, d), 9.58 (1H, s), 10.17 (1H, s). LCMS: m/z 425.2 [M+H] ⁺ Example 38.1-Acetyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)pheny l)- pyrrolidine-3-carboxamide (Compound 412) N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)pyrrolidin e-3- carboxamide (74 mg, 1 Eq., 1.321 mmol) and Et ₃ N (271 μL, 10 eq., 1.945 mmol) were dissolved in DCM (5 mL) under nitrogen. Acetyl chloride was added dropwise at 0 °C and the mixture was stirred and gradually raised to RT. After completion the reaction, the mixture was diluted with EtOAc (20 ml) and washed with brine (2×10 ml). The organic phase was dried over sodium sulfate, filtered and concentrated. The crude residue was purified further with reverse phase chromatography to obtain 36 mg of the title compound. ¹ H NMR (400 MHz, CDCl3 mixture of rotamers in ~ 1.0:1.2 ratio) δ: 8.19 (m, 1H), 7.93 (br s, 0.45H), 7.88 (br s, 0.52H), 7.57-7.50 (m, 2.1H), 7.02-6.94 (m, 2.1H), 6.90 (m, 1.1H), 6.78 (m, 1H), 3.93 (s, 1.54H), 3.92 (s, 1.72H), 3.91-3.84 (m, 0.59H), 3.81-3.65 (m, 2.7H), 3.55-3.42 (m, 1.12H), 3.16 (m, 0.5H), 3.06 (quin, 0.58H) 2.45-2.34 (m, 0.67H), 2.31-2.16 (m, 1.8H), 2.08 (s, 1.44H), 2.07 (s, 1.63H). LCMS: m/z 423.2 [M+H] ⁺ The following compounds were prepared according to the procedure described for Compound 412. The compound code, structure, starting materials, purification method and characterization data are indicated in the table. Example 39.1-Glycyl-N-(2-methoxy-5-(4-(trifluoromethyl)phenoxy)pheny l)-5- oxopyrrolidine-2-carboxamide, HCl (Compound 414) In a Büchner flask benzyl (2-(2-((2-methoxy-5-(4-(trifluoromethyl)phenoxy)- phenyl)carbamoyl)-5-oxopyrrolidin-1-yl)-2-oxoethyl)carbamate (168 mg, 0.287 mmol, 1 eq.) was dissolved in EtOH (10 ml) and palladium (24.4 mg, 0.023 mmol, 0.08 eq.) and HCl (37 %, 0.120 ml, 1.435 mmol, 5 eq.) was added. The flask was connected to a H ₂ /N ₂ /vacuum line and after replacement of air with nitrogen, the mixture was stirred under hydrogen for 2.5 h. The mixture was filtered through a pad of Celite ^® and washed with a 1:1 mixture of acetonitrile/H ₂ O. The product was frozen at -78 °C and solvents removed on freeze dryer to obtain the title compound. ¹ H NMR (400 MHz, DMSO-d6) δ: 9.91 (s, 1H), 8.17 (br.s, 1H), 7.85 (d, 1H), 7.70 (d, 2H), 7.15 (d, 1H), 7.06 (d, 2H), 6.93 (dd, 1H), 5.15 (m, 1H), 4.20 (d, 1H), 4.17 (d, 1H), 3.91 (s, 3H), 2.71-2.30 (m, 3H), 2.04 (m, 1H). LCMS: m/z 452.598 [M+H] ^+. Example 40. (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)- pyrrolidine-2-carboxamide (Compound 415) The compound was prepared according to the procedure described for Intermediate 364 starting from tert-butyl (S)-2-((2-methoxy-5-(4-(trifluoromethyl)- phenoxy)phenyl)carbamoyl)-5-oxopyrrolidine-1-carboxylate. The crude end product was treated with saturated Na2CO3 solution and then extracted with DCM. The organic phase was dried and evaporated to obtain the title compound. ¹ H NMR (400 MHz, CDCl ₃ ) δ: 10.2 (s, 1H), 8.27 (d, 1H), 7.48-7.56 (m, 2H), 6.96-7.03 (m, 2H), 6.87 (d, 1H), 6.74 (dd, 1H), 3.91 (s, 3H), 3.85-3.92 (m, 1H), 2.98-3.15 (m, 2H), 2.14-2.26 (m, 1H), 1.97-2.08 (m, 1H), 1.68-1.85 (m, 2H). LCMS: m/z 381.7 [M+H] ⁺ Example 41. (S)-N-(5-((3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)oxy)-2- methoxyphenyl)pyrrolidine-2-carboxamide (Compound 416) The compound was prepared according to the procedure described for Intermediate 364 starting from tert-butyl (2S)-2-((5-((3-fluoro-5-(trifluoromethyl)- pyridin-2-yl)oxy)-2-methoxyphenyl)carbamoyl)-1l4-pyrrolidine -1-carboxylate. The crude end product was treated with saturated Na2CO3 solution and then extracted with DCM. The organic phase was dried and evaporated to obtain the title compound. ¹ H NMR (400 MHz, CDCl3) δ: 10.2 (s, 1H), 8.37 (d, 1H), 8.14-8.19 (m, 1H), 7.64 (dd, 1H), 6.91 (d, 1H), 6.86 (dd, 1H), 3.92 (s, 3H), 3.86 (dd, 1H), 2.96-3.14 (m, 2H), 2.13 (br, 1H), 2.12-2.24 (m, 1H), 1.96-2.07 (m, 1H), 1.67-1.84 (m, 2H). LCMS: m/z 400.6 [M+H] ⁺ Example 42. (S)-N-(2-Methoxy-5-(4-(trifluoromethyl)phenoxy)phenyl)-N,1- dimethyl-5-oxopyrrolidine-2-carboxamide (Compound 417) To a cooled (0-5 ºC) solution of (S)-N-(2-methoxy-5-(4-(trifluoromethyl)- phenoxy)phenyl)-1-methyl-5-oxopyrrolidine-2-carboxamide (0.204 g, 0.50 mmol) in dry DMF (2.0 mmol) was added sodium hydride, 60 wt-% in oil (0.025 g, 0.625 mmol) followed by stirring the mixture at 0-5 ºC for 15 min. Iodomethane (0.062 ml, 1.00 mmol) was added and stirring was continued at RT until reaction was completed. The mixture was diluted with water and extracted with EtOAc. Organic phase was washed with water and brine, dried and evaporated. Crude product was purified by reverse phase flash chromatography to afford the title compound. Yield: 0.152 g. ¹ H NMR (400 MHz, CDCl ₃ ), mixture of rotamers. Chemical shifts for the main rotamer: δ: 7.56-7.64 (m, 2H), 7.07-7.14 (m, 1H), 6.98-7.06 (m, 3H), 6.96 (dd, 1H), 3.93 (dd, 1H), 3.90 (s, 3H), 3.21 (s, 3H), 2.76 (s, 3H), 2.43-2.62 (m, 1H), 2.18-2.31 (m, 1H), 1.77-2.08 (m, 2H). LCMS: m/z 423.4 [M+H] ⁺ . Abbreviations DCM – Dichloromethane DEAD – Diethyl azodicarboxylate DIPEA – N,N-diisopropylethylamine DMA – Dimethylacetamide DMAP – 4-Dimethylaminopyridine DMF – N,N-Dimethylformamide DMSO – Dimethylsulfoxide ee – Enantiomeric excess eq. – Molar equivalent GCMS – Gas chromatography–mass spectrometry HATU – 2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluoro- phosphate HPLC – High-performance liquid chromatography LCMS – Liquid chromatography–mass spectrometry LiHMDS – Lithium bis(trimethylsilyl)amide MTBE – Methyl tert-butyl ether Pd ₂ (dba) ₃ – Tris(dibenzylideneacetone)dipalladium PdCl ₂ (dppf) – [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II ) RT – Room temperature rt – Retention time SPhos Pd G2 – Chloro(2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-bi phenyl)[2-(2′- amino-1,1′-biphenyl)]palladium(II) T ₃ P – 1-propanephosphonic acid cyclic anhydride TBAF – Tetra-n-butylammonium fluoride TEA – Triethylamine TFA – Trifluoroacetic acid THF – Tetrahydrofuran TMA – trimethylaluminium TMS-Cl – Trimethylsilyl chloride XantPhos – 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene EXPERIMENTS Experiment 1. TEAD inhibition TEAD inhibition was assayed using Hippo Pathway TEAD Reporter – MCF-7 cell line (BPS Bioscience, Catalog #: 60618) which contains firefly luciferase gene under the control of TEAD responsive elements. In the cell line, YAP1 remains in the nucleus inducing constitutive expression of luciferase reporter. Amount of expressed luciferase was detected using ONE-Glo Luciferase Assay System (Promega) and measuring plates with Enspire Multimode Plate Reader (PerkinElmer). Hippo Pathway TEAD Reporter – MCF-7 cells were plated on white/clear Poly- D-Lysine coated 384 plates (Corning # 356660) at the density of 8500 cells/well. Next day test compounds (11 concentrations with 4 replicates) and DMSO control (0.1 %) were added to the plate. After 24 h cells were lysed and luciferase activity was measured. The half maximal inhibitory concentration ( IC ₅₀ ) of the test compounds on YAP-TEAD inhibition was determined. The compounds of the invention were screened in the above mentioned assay and the IC ₅₀ values of the compounds are set forth in Table 1 below wherein “A” refers to a group of compounds having IC ₅₀ value of less than 50 nM, “B” refers to a group of compounds having IC ₅₀ value in range of 50 to 300 nM and “C” refers to a group of compounds having IC ₅₀ value in range of 301 nM to 2000 nM.

Table 1.