The present invention relates to benzofurane and benzothiophene derivatives of formula (I) and their use in the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor. The present invention further relates to novel benzofurane and benzothiophene derivatives of formula (II) and their use as pharmaceuticals. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more compounds of formula (I) / formula (II), and their use as modulators of the PGE2 receptors EP2 (alias PTGER2, alias PGE2 Receptor EP2 Subtype) and/or EP4 (alias PTGER4, alias EP4R, alias PGE2 Receptor EP4 Subtype). The compounds of formula (I) / formula (II) may especially be used as single agents or in combination with one or more therapeutic agents and/or chemotherapy and/or radiotherapy and/or immunotherapy in the prevention/prophylaxis or treatment of cancers; in particular the prevention/prophylaxis or treatment of melanoma; lung cancer; bladder cancer; renal carcinomas; gastro-intestinal cancers; endometrial cancer; ovarian cancer; cervical cancer; and neuroblastoma.

Prostaglandin E2 (PGE2) is a bioactive lipid that can elicit a wide range of biological effects associated with inflammation and cancer. PGE2 belongs to the prostanoid family of lipids. Cyclooxygenase (COX) is the rate-limiting enzyme in the synthesis of biological mediators termed prostanoids, consisting of prostaglandin PGD2, PGE2, PGF2a, prostacyclin PGI2, and thromboxane TXA2. Prostanoids function via activation of seven transmembrane G-protein-coupled receptors (GPCRs), in particular EP1 , EP2, EP3, and EP4 are receptors for PGE2. Activation of both EP2 and EP4 by PGE2 stimulates adenylate cyclase, resulting in elevation of cytoplasmic cAMP levels to initiate multiple downstream events via its prototypical effector Protein kinase A. In addition, PGE2 is also able to signal via PI3K/AKT and Ras-MAPK/ERK signalling

Cancers figure among the leading causes of death worldwide. Tumors are comprised of abnormally proliferating malignant cancer cells but also of a functionally supportive microenvironment. This tumor microenvironment is comprised of a complex array of cells, extracellular matrix components, and signaling molecules and is established by the altered communication between stromal and tumor cells. As tumors expand in size, they elicit the production of diverse factors that can help the tumor to grow such as angiogenic factors (promoting ingrowth of blood vessels) or that can help to evade the attack of the host immune response. PGE2 is such an immuno-modulatory factor produced in tumors.

It is well established that COX2, mainly via PGE2, promotes overall growth of tumors and is upregulated and correlates with clinical outcome in a high percentage of common cancers, especially colorectal, gastric, esophageal, pancreatic, breast and ovarian cancer. High COX-2 and PGE2 expression levels are associated with neoplastic transformation, cell growth, angiogenesis, invasiveness, metastasis and immune evasion.

The finding that COX2 is over-expressed and plays an important role in carcinogenesis in gastrointestinal (Gl) cancers including among others esophagus, gastric and colorectal cancers has led to the fact that COX-inhibitors (Coxibs), including Celecoxib, and other nonsteroidal anti-inflammatory drugs (NSAID), including aspirin, are among the most studied cancer chemopreventive agents in development today (for review see for example Wang R et al, Curr Pharm Des. 2013; 19(1 ): 1 15-25; Garcia Rodriguez LA et al, Recent Results Cancer Res. 2013; 191 :67- 93, Sahin IH et al, Cancer Lett. 2014 Apr 10;345(2):249-57; Drew DA et al, Nat Rev Cancer 2016, 16:173; Brotons C et al, Am J Cardiovasc Drugs. 2015 Apr; 15(2):1 13)

In addition to COX2 and PGE2, also EP receptors, especially EP2 and EP4, are aberrantly over-expressed in multiple types of cancers, especially in gastro-intestinal (Gl) cancers and pancreatic cancer. Furthermore, the over- expression of PGE2 and/or EP2 and/or EP4 correlates with diseases progression in some cancer types such as oesophageal squamous cell carcinoma (Kuo KT et al, Ann Surg One 2009; 16(2), 352-60); squamous cell carcinoma of the lung (Alaa M et al, Int J Oncol 2009, 34(3); 805-12); prostate cancer (Miyata Y et al, Urology 2013, 81 (1 ): 136-42); Badawi AF and Badr MZ Int J Cancer. 2003, 103(1 ):84-90); head and neck squamous cell carcinoma (Gallo O et al, Hum Pathol. 2002, 33(7)708-14).

In accordance to studies performed with Coxibs, in mice, knockout of either COX1 , COX2, microsomal prostaglandin E synthase 1 (mPTGESI ), EP2 or EP4 resulted in reduced tumor incidence and progression in different tumor models. Conversely, overexpression of COX2 or mPTGESI in transgenic mice resulted in increased tumor incidence and tumor burden (for review see Nakanishi M. and Rosenberg D.W., Seminars in Immunopathology 2013, 35: 123-137; Fischer SM et al Cancer Prev Res (Phila) 201 1 Nov;4(1 1 ):1728-35; Fulton AM et al Cancer Res 2006; 66(20); 9794-97).

Several pharmacological studies to inhibit tumor growth and progression using EP receptor antagonists or COX2 inhibitors in different tumor models have been conducted in mice. Among others, EP antagonists and/or COX2 inhibitors reduced tumor growth and metastasis in experimental models of colorectal cancer (e.g Yang L et al Cancer Res 2006, 66(19), 9665-9672; Pozzi A.et al JBC 279(28); 29797-29804), lung carcinomas (Sharma S et al Cancer Res 2005 65(12), 521 1-5220), gastro-intestinal cancer (Oshima H et al Gastroenterology 201 1 , 140(2); 596-607; Fu SL et al world J Gastroenterol 2004, 10(13); 1971-1974), breast cancer (Kundu N et al, Breast Cancer Res Treat 1 17, 2009; 235-242; Ma X et al, Oncolmmunology 2013; Xin X et al Lab Investigation 2012, 1-14; Markosyan N et al; Breast Cancer Res 2013, 15:R75), prostate cancer (Xu S et al, Cell Biochem Biophys 2014, Terada et al Cancer Res 70(4) 2010; 1606-1615), pancreatic cancer (Al-Wadei HA et al, PLOS One 2012, 7(8):e43376; Funahashi H et al, Cancer Res 2007, 67(15):7068-71 ). COX2 inhibitors were approved for the treatment of familial adenomatous polyposis (FAP) which is an inherited pre-disposition syndrome for colorectal cancer, but later retracted due to cardiovascular side effects.

Mechanistically, PGE2 signalling is mainly involved in the crosstalk between tumor and stromal cells, thereby creating a microenvironment which is favourable for the tumor to grow. In particular, PGE2 signalling via EP2 and EP4 can for example (i) suppress the cytotoxicity and cytokine production of natural killer cells, (ii) skew the polarization of tumor-associated macrophages towards tumor-promoting M2 macrophages (see for example Nakanishi Y et al Carcinogenesis 2011 , 32:1333-39), (iii) regulate the activation, expansion and effector function of both Tregs (regulatory T cells) and MDSC (myeloid derived suppressor cells), which are potent immunosuppressive cells that accumulate in tumors both in patients and in experimental animal models (see for example Sharma S et al, Cancer Res 2005, 5(12):521 1-20; Sinha P et al Cancer Res 2007, 67(9), 4507-4513; Obermajer N et al, Blood 201 1 , 1 18(20):5498-5505); (iv) down-regulate IFN-γ, TNF-a IL-12 and IL-2 expression in immune cells such as natural killer cells, T-cells, dendritic cells and macrophages, impairing the ability of these immune cells to induce tumor cell apoptosis and restrain tumorigenesis (see for example Bao YS et al, Int Immunopharmacol. 201 1 ;1 1 (10):1599-605; Kim JG and Hahn YS, Immunol Invest. 2000;29(3):257-69; Demeuere CE et al, Eur J Immunol. 1997;27(12):3526-31 ; Mitsuhashi M et al, J Leukoc Biol. 2004;76(2):322-32; Pockaj BA et al , Ann Surg Oncol. 2004;11 (3):328-39; (v) suppress activation, IL-2 responsivness, expansion and cytotoxicity of T-cells thereby contributing to local immunsuppresion (see for example Specht C et al, Int J Cancer 200191 :705-712); (vi) inhibit maturation of dendritic cells, their ability to present antigens and to produce IL-12, resulting in abortive activation of cytotoxic T-cells (see for example Ahmadi M et al, Cancer Res 2008, 68(18):7250-9; Stolina M et al, J Immunol 2000, 164:361 -70); (vii) regulate tumor angiogenesis (formation of new blood vessels for nutrient and oxygen supply) by enhancing endothelial cell motility and survival as well as by increasing the expression of VEGF (vascular endothelial growth factor) (see for example Zhang Y and Daaka Y, Blood 2011 ;1 18( 9):5355-64; Jain S et al, Cancer Res. 2008; 68(19):7750-9; Wang and Klein, Molecular Carcinogenesis 2007, 46:912-923; (viii) enhance tumor cell survival (via PI3K/AKT and MAPK signalling). For review see for example Kalinski P, J Immunol 2012, 188(1 ), 21-28; Obermajer N et al, Oncoimmunology 1 (5), 762-4; Greenhough A et al, carcinogenesis 2009, 30(3), 377-86; Wang D and Dubois RN, Gut 2006, 55, 1 15-122; Harris SG e al Trends Immunol 2002, 22, 144-150).

Coxibs have been shown to render tumor cells more sensitive to radiation and chemotherapy and several clinical trials have been performed or are ongoing combining Coxibs with radio- and/or chemotherapy (for review see e.g Ghosh N et al, Pharmacol Rep. 2010 Mar-Apr;62(2):233-44; Davis TW et al, Am J Clin Oncol. 2003, 26(4):S58-61 ; see also Higgins JP et al, Cancer Biol Ther 2009, 8:1440-49).

Furthermore, there is some evidence of additive effects and/or synergy between Coxibs and epidermal growth factor receptor (EGFR) inhibitors (see for example Zhang X et al, Clin Cancer Res. 2005, 11 (17):6261 -9; Yamaguchi NH et al, J Gastrointest Oncol. 2014, 5(1 ):57-66); and with aromatase inhibitors (see for example Generali D et al, Br J Cancer. 2014;11 1 (1 ):46-54; Lustberg MB et all, Clin Breast Cancer. 2011 Aug;1 1 (4):221-7; Falandry C et al, Breast Cancer Res Treat. 2009 Aug;116(3):501-8); Chow LW et al, J Steroid Biochem Mol Biol. 2008, 1 11 (1-2):13-7).

Moreover, additive/synergistic effects have been seen in different mouse tumor models when Aspirin (a COX1/2 inhibitor) was combined with and anti-VEGF antibody (Motz GT et al; Nat Med 201420(6):607) and this combination is currently under investigation in clinical trials (NCT02659384).

Recently, it has been shown that, if combined, different immunotherapeutic approaches can have enhanced antitumor efficacy. Due to the immune-modulatory properties of PGE2, Coxibs have thus also been used in combination with different immunotherapeutic approaches. In particular, additive or even synergistic effects could be observed when Coxibs were combined with dendritic cell vaccination in a rat glioma model and in a mouse mesothelioma or melanoma model (Zhang H et al, Oncol Res. 2013;20(10):447-55; Veltman JD et al, BMC Cancer. 2010;10:464; Toomey D et all, Vaccine. 2008 Jun 25;26(27-28):3540-9); with granulocyte-macrophage colony-stimulating factor (GM-CSF) in mouse brain tumors (Eberstal S et al, Int J Cancer. 2014 Jun 1 ;134(1 1 ):2748-53); with interferon gamma (IFN-γ) in brain tumors (Eberstal S et al, Cancer Immunol Immunother. 2012, 61 (8):1 191-9); with dendritic cell vaccination or with GM-CSF in a mouse breast cancer model (Hahn T et al, Int J Cancer. 2006, 118(9):2220- 31 ); and with adenoviral interferon beta (IFN-β) therapy in a mouse mesothelioma model (DeLong P et al, Cancer Res. 2003 Nov 15;63(22):7845-52). Along these lines, additive or even synergistic effects of Coxibs and/or EP2 and/or EP4 antagonists can also be envisaged with agents acting on cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) such as anti-CTLA-4 antibodies; anti-TIM-3 antibodies, anti-Lag-3 antibodies; anti-TIGIT antibodies; or, in particular, with agents acting on programmed cell death protein 1 (PD1 ), such as anti-PD1 or anti-PDL1 (programmed cell death ligand 1 ) antibodies (Yongkui Li et al Oncoimmunology 2016, 5(2):e1074374; Zelenay S et al, Cell 2015, 162; 1-14; WO2013/090552, which indicates a synergistic effect of dual EP2 and EP4 blockade in combination with agents acting on PD1J.

Adenosine is another endogenous factor with anti-inflammatory properties that is generated through the activity of ectonucleotidases, CD39 and CD73, expressed on various cell types, including regulatory T cells (Treg) (Mandapathil M et al, J Biol Chem. 2010; 285(10):7176-86). Immune cells also respond to Adenosine, because they bear receptors for ADO, which are mainly of the A2a/A2b type (Hoskin DW, et al, Int J Oncol 2008, 32:527- 535). Signaling via Adenosine receptors and EP2/EP4 receptors converges on the cytoplasmic adenylyl cyclase, leading to up-regulation of cAMP. It was shown that Adenosine and PGE2 cooperate in the suppression of immune responses mediated by regulatory T cells (Mandapathil M et al, J Biol Chem. 2010; 285(36):27571-80; Caiazzo E et al, Biochem Pharmacol. 2016; 1 12:72-81 ).

Thus, the present EP2 and/or EP4 antagonists may be useful, alone, or in combination with with one or more therapeutic agents and/or chemotherapy and/or radiotherapy and/or immunotherapy; in particular in combination with chemotherapy, radiotherapy, EGFR inhibitors, aromatase inhibitors, anti-angiogenic drugs, adenosine inhibitors, immunotherapy such as especially PD1 and/or PDL1 blockade, or other targeted therapies; for the prevention / prophylaxis or treatment of cancers, notably for the prevention / prophylaxis or treatment of skin cancer including melanoma including metastatic melanoma; lung cancer including non-small cell lung cancer; bladder cancer including urinary bladder cancer, urothelial cell carcinoma; renal carcinomas including renal cell carcinoma, metastatic renal cell carcinoma, metastatic renal clear cell carcinoma; gastro-intestinal cancers including colorectal cancer, metastatic colorectal cancer, familial adenomatous polyposis (FAP), oesophageal cancer, gastric cancer, gallbladder cancer, cholangiocarcinoma, hepatocellular carcinoma, and pancreatic cancer such as pancreatic adenocarcinoma or pancreatic ductal carcinoma; endometrial cancer; ovarian cancer; cervical cancer; neuroblastoma; prostate cancer including castrate-resistant prostate cancer; brain tumors including brain metastases, malignant gliomas, glioblastoma multiforme, medulloblastoma, meningiomas; breast cancer including triple negative breast carcinoma; oral tumors; nasopharyngeal tumors; thoracic cancer; head and neck cancer; leukemias including acute myeloid leukemia, adult T-cell leukemia; carcinomas; adenocarcinomas; thyroid carcinoma including papillary thyroid carcinoma; choriocarcinoma; Ewing's sarcoma; osteosarcoma; rhabdomyosarcoma; Kaposi's sarcoma; lymphoma including Burkitt's lymphoma, Hodgkin's lymphoma, MALT lymphoma; multiple myelomas; and virally induced tumors.

In addition, selective or dual EP2 and/or EP4 antagonists may be useful in several other diseases or disorders responding for example to treatment with COX2 inhibitors, with the advantage that EP2 and/or EP4 antagonists should not possess the potential cardiovascular side effects seen with C0X2 inhibitors, which are mainly due to interference with PGI2 and TXA2 synthesis (see for example Boyd MJ et al, bioorganic and medicinal chemistry letters 21 , 484, 201 1 ). For example, blockade of prostaglandin production by COX inhibitors is the treatment of choice for pain, including especially inflammatory pain and painful menstruation. Thus EP2 and/or EP4 and/or dual EP2/EP4 antagonists may be useful for the treatment of pain, especially inflammatory pain. Evidence from EP2 knockout mice suggest that EP2 antagonists can be used for the treatment of inflammatory hyperalgesia (Reinold H et al, J Clin Invest 2005, 1 15(3):673-9). In addition, EP4 antagonists have beneficial effect in vivo in inflammatory pain models (eg Murase A, Eur J Pharmacol 2008; Clark P, J Pharmacol Exp Ther. 2008; Maubach KA Br J Pharmacol. 2009; Colucci J Bioorg Med Chem Lett. 2010, Boyd MJ et al, Bioorg Med Chem Lett 201 1 , Chn Q et al Br J Phramacol 2010, Nakao K et al, J Pharmacol Exp Ther. 2007 Aug;322(2):686-94). Administration of an EP2 in combination with an EP4 antagonist showed significant, but partial inhibition of joint inflammation in mouse collagen-induced arthritis model (Honda T et al J Exp Med 2006, 203(2):325-35).

EP2 and/or dual EP2/EP4 antagonists may be of use to decrease female fertility, i.e. they have been shown to prevent pregnancy if used as contraceptive in macaques (Peluffo MC et al Hum Reprod 2014). EP2 knockout mice have decreased fertility, smaller litter sizes and reduced cumulus expansion (Matsumoto et al, Biology of reproduction 2001 , 64; 1557-65; Hitzaki et al, PNAS 1999, 96(18), 10501 -10506; Tilley SL J Clin Inves 1999, 103(1 1 ):1539-45; Kennedy CR et al, Nat Med 1999 5(2):217-20).

There is also rationale that EP2 and/ or EP4 antagonists may be of use to prevent or treat endometriosis: for example EP2, EP3 and EP4 and COX2 are overexpressed in endometriosis cell lines and tissues (e.g. Santulli P et al J Clin Endocrinol Metab 2014, 99(3):881-90); antagonist treatment was shown to inhibit the adhesion of endometrial cells in vitro (Lee J et al Biol Reprod 2013, 88(3):77; Lee J et al Fertil Steril 201 , 93(8):2498-506); COX2 inhibitors have been shown to reduce endometric lesions in mice via EP2 (Chuang PC et al, Am J Pathol 2010, 176(2):850-60); and antagonist treatment has been shown to induce apoptosis of endometric cells in vitro (Banu SK et al, MOI endocrinol 2009, 23(8) 1291 -305).

Dual EP2/EP4 antagonists, or the combination of a selective EP2 antagonists with a selective EP4 antagonist, may be of potential use for autoimmune disorders; e.g. they have been shown to be effective in mouse model for multiple sclerosis (MS) (Esaki Yet al PNAS 2010, 107(27):12233-8; Schiffmann S et al, Biochem Pharmacol. 2014, 87(4): 625-35; see also Kofler DM et al J Clin Invest 2014, 124(6):2513-22). Activation of EP2 / EP 4 signalling in cells in vitro (Kojima F et al Prostaglandins Other Lipid Mediat 2009, 89:26-33) linked dual or selective EP2 and/or EP4 antagonists to the treatment of rheumatoid arthritis. Also, elevated levels of PGE(2) have been reported in synovial fluid and cartilage from patients with osteoarthritis (OA) and it has been shown that PGE2 stimulates matrix degradation in osteoarthitis chondrocytes via the EP4 receptor (Attur M et al, J Immunol. 2008;181 (7):5082-8).

EP4 overexpression is associated with enhanced inflammatory reaction in atherosclerotic plaques of patients (Cipollone F et al, Artherioscler Thromb Vase Biol 2005, 25(9); 1925-31 ), thus the use of EP4 and/or dual EP2/EP4 antagonists may be indicated for plaque stabilization and prevention / prophylaxis of acute ischemic syndromes. In addition, EP4 deficiency suppresses early atherosclerosis, by compromising macrophage survival (Babaev VR et al, Cell Metab. 2008 Dec;8(6):492-501 )

EP2 and/or dual EP2/EP4 antagonists may also be useful in the treatment of pneumonia: intrapulmonary administration of apoptotic cells demonstrated that PGE(2) via EP2 accounts for subsequent impairment of lung recruitment of leukocytes and clearance of Streptococcus pneumoniae, as well as enhanced generation of IL-10 in vivo (Medeiros Al et al J Exp Med 2009 206(1 ):61 -8).

EP2 and/or dual EP2/EP4 antagonists may in addition be useful for the treatment of neurodegenerative diseases (for review see Cimino PJ et al, Curr Med Chem. 2008;15(19):1863-9). EP2 receptor accelerates progression of inflammation in a mouse model of amyotrophic lateral sclerosis (ALS) (Liang X et al, Ann Neurol 2008, 64(3):304- 14); COX2 inhibitors have been shown to be neuroprotective in rodent models of stroke, Parkinson disease and ALS (for review see Liang X et al J Mol Neurosci 2007, 33(1 ):94-9), decreased neurotoxicity was observed in EP2 knockout mice treated with parkinsonian toxican (Jin J et al, J Neuroinflammation 2007, 4:2), PGE2 via EP2 aggravates neurodegeneration in cultured rat cells (Takadera T et al, Life Sci 2006, 78(16): 1878-83); Reduced amyloid burden was observed in Alzheimer's disease mouse model if crossed with EP2 knockout mice (Liang X et al J Neurosci 2005, 25(44):10180-7; Keene CD etal, Am J Pathol. 2010, 177(1 ):346-54). EP2 null mice are protected from CD14-dependent innate immunity mediated neuronal damage in neurodegenerative disease (Shie FS et al Glia 2005, 52(1 ):70-7); PGE2 via EP2 increases amyloid precursor protein (APP) expression in cultured rat microglial cells (Pooler AM et al Neurosci. Lett. 2004, 362(2): 127-30). EP2 antagonist limits oxidative damage from activation of innate immunity (intracranial injection of LPS) in the brain and could be used for Alzheimer or HIV associated dementia (Montine TJ et al, J Neurochem 2002, 83(2):463-70). In an Alzheimer's disease mouse model cognitive function could be improved by genetic and pharmacological inhibition of EP4 (Hoshino T et al, J Neurochem 2012, 120(5):795-805).

EP2 and/or dual EP2/EP4 antagonists may also be useful to treat autosomal dominant polycystic kidney disease (ADPKD): PGE2 via EP2 induces cystogenesis of human renal epithelial cells; and EP2 was found to be overexpressed in patient samples (Elberg G et al, Am J Physiol Renal Physiol 2007, 293(5):F1622-32).

EP4 and/or dual EP2/EP4 antagonists may also be useful to treat osteoporosis: PGE2 stimulates bone resorption mainly via EP4 and partially via EP2 (Suzawa T et all, Endocrinology. 2000 Apr; 141 (4): 1554-9), EP4 knockout mice show impaired bone resorption (Miyaura C et al, J Biol Chem 2000, 275(26): 19819-23) and an EP4 antagonists showed partial inhibition of PGE(2)-stimulated osteoclastogenesis and osteoclastic bone resorption (Tomita M et al, Bone. 2002 Jan;30(1 ):159-63). WO2008/152093 discloses selective EP2 receptor modulators which comprise an indole ring linked to the rest of the molecule in position 3, and a pyrimidine moiety which however is not substituted with a directly linked aromatic substituent. WO2006/044732 discloses pyrimidine compounds which are modulators of PGD2 claimed to be useful e.g. in the treatment of allergic diseases; however for example the exemplified compound CAS 1001913-77-4 has been tested to be inactive on both the EP2 and the EP4 receptor in the in vitro assay set out in the experimental part below. WO2008/006583 discloses pyrimidin derivatives which are ALK-5 inhibitors. WO2006/044732 and WO2008/039882 disclose certain pyrimidine derivatives as protaglandin D2 receptor antagonists. Pyrimidin-2-yl derivatives are disclosed in WO2013/020945, WO2012/127032, WO201 1/144742, WO201 1/022348, WO2009/105220, Bioorg. Med. Chem 2011 , 21 (13) 4108-41 14 and Bioorg. Med. Chem 201 1 , 21 (1 ) 66-75. Further compounds which are claimed to be active as anti-cancer agents are disclosed in WO2006/128129, WO2008/008059 and Bioorg. Med. Chem 2013, 21 (2), 540-546. WO2013/163190 WO2015/058067, and WO2015/058031 disclose certain DNA-PK inhibitors interacting with DNA repair processes. The disclosed compounds are thought to be useful to sensitize cancer cells by directly modulating cancer cell proliferation, and to enhance the efficacy of both cancer chemotherapy and radiotherapy.

The present invention provides novel benzofurane and benzothiophene derivatives of formula (I) / formula (II) which are modulators of the prostaglandin 2 receptors EP2 and/or EP4. Certain compounds of the present invention are dual antagonists of both the EP2 and the EP4 receptor. The present compounds may, thus, be useful for the prevention / prophylaxis or treatment of diseases which respond to the blockage of the EP2 receptors and/or the EP4 receptors such as especially cancers, wherein a particular aspect is the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor; as well as pain including especially inflammatory pain and painful menstruation; endometriosis; acute ischemic syndromes in atherosclerotic patients; pneumonia; neurodegenerative diseases including amyotrophic lateral sclerosis, stroke; Parkinson disease, Alzheimer's disease and HIV associated dementia; autosomal dominant polycystic kidney disease; and to control female fertility.

1 ) A first aspect of the invention relates to compounds of the formula (I)

Formula (I)

for use in the treatment of a cancer, wherein said cancer is treated by modulating an immune response comprising a reactivation of the immune system in the tumor; wherein said cancer is notably a cancer selected from melanoma including metastatic melanoma; lung cancer including non-small cell lung cancer; bladder cancer including urinary bladder cancer, urothelial cell carcinoma; renal carcinomas including renal cell carcinoma, metastatic renal cell carcinoma, metastatic renal clear cell carcinoma; gastro-intestinal cancers including colorectal cancer, metastatic colorectal cancer, familial adenomatous polyposis (FAP), oesophageal cancer, gastric cancer, gallbladder cancer, cholangiocarcinoma, hepatocellular carcinoma, and pancreatic cancer such as pancreatic adenocarcinoma or pancreatic ductal carcinoma; endometrial cancer; ovarian cancer; cervical cancer; neuroblastoma; prostate cancer including castrate- resistant prostate cancer; brain tumors including brain metastases, malignant gliomas, glioblastoma multiforme, medulloblastoma, meningiomas; breast cancer including triple negative breast carcinoma; oral tumors; nasopharyngeal tumors; thoracic cancer; head and neck cancer; leukemias including acute myeloid leukemia, adult T-cell leukemia; carcinomas; adenocarcinomas; thyroid carcinoma including papillary thyroid carcinoma; choriocarcinoma; Ewing's sarcoma; osteosarcoma; rhabdomyosarcoma; Kaposi's sarcoma; lymphoma including Burkitt's lymphoma, Hodgkin's lymphoma, MALT lymphoma; multiple myelomas; and virally induced tumors (especially such cancer is selected from melanoma; lung cancer; bladder cancer; renal carcinomas; gastrointestinal cancers; endometrial cancer; ovarian cancer; cervical cancer; and neuroblastoma);

wherein said compound is optionally used in combination with one or more chemotherapy agents and / or radiotherapy and / or targeted therapy;

wherein in compounds of the formula (I)

the fragment

is substituted with R ² , wherein R ² represents hydrogen, (especially methyl, ethyl), halogen (especially chloro, bromo), or cyano; and

is optionally substituted with (R ¹ ) _n ; wherein (R ¹ ) _n represents one, two or three optional substituents (i.e. said fragment is, in addtition to R ² , unsubstituted, or substituted with one, two or three R ¹ ), wherein said substituents R ¹ are independently selected from (Ci-3)alkyl (especially methyl), (Ci-3)alkoxy (especially methoxy), halogen (especially fluoro, or chloro), (Ci-3)fluoroalkyl (especially trifluoromethyl), (Ci-3)fluoroalkoxy (especially trifluoromethoxy), or cyano; (for avoidance of any doubt: substituents (R ¹ ) _n are in addition to the substituent R ² as defined above);

X represents S or 0; R ³ represents hydrogen, methyl or trifluoromethyl (especially hydrogen);

R ^4a and R ^4b independently represent hydrogen, methyl, or R ^4a and R ^4b together with the carbon atom to which they are attached represent a cycloprop-1 , 1 -diyl group;

R ^5a and R ^5b independently represent hydrogen, methyl, or R ^5a and R ^5b together with the carbon atom to which they are attached represent a cycloprop-1, 1 -diyl group;

Ar ¹ represents

• phenyl, or 5- or 6-membered heteroaryl (notably 5-membered heteroaryl, especially thiophenyl or thiazolyl); wherein said phenyl or 5- or 6-membered heteroaryl independently is mono-, di- or tri-substituted, wherein the substituents are independently selected from

• (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, 1 -methyl-propan-1 -yl, tert.- butyl, 3-methyl-butyl);

• (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy);

• (Ci-3)fluoroalkyl, wherein said (Ci-3)fluoroalkyl is optionally substituted with hydroxy (especially trifluoromethyl, 2,2,2-trifluoro-1-hydroxy-ethyl);

• (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

• halogen (especially fluoro, chloro, bromo);

• cyano;

• (C3-6)cycloalkyl, wherein said (C3-6)cycloalkyl is unsubstituted or mono-substituted with amino (especially cyclopropyl, 1-amino-cyclopropyl);

• (C4-6)cycloalkyl containing a ring oxygen atom, wherein said (C4-6)cycloalkyl containing a ring oxygen atom is unsubstituted or mono-substituted with hydroxy (especially 3-hydroxy-oxetan-3-yl);

• (C3-6)cycloalkyl-oxy (especially cyclobutyl-oxy, cyclopentyl-oxy);

• hydroxy;

• -X -CO-R ⁰¹ , wherein

^■ X ¹ represents a direct bond, (Ci. ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-,-C(CH ₃ ) ₂ -,-CH ₂ -CH ₂ - ), -0-(Ci- ₃ )alkylene- ^* (especially -0-CH ₂ -*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), - NH-(Ci- ₃ )alkylene- ^* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -S-CH ₂ -*, -CF ₂ -, -CH=CH-, - CH≡CH-, -NH-CO-*, -CO-, or (C3- ₅ )cycloalkylene; wherein the asterisks indicate the bond that is linked to the -CO-R ⁰¹ group; and

^■ R ⁰¹ represents

• -OH;

• -0-(Ci )alkyl (especially ethoxy, methoxy);

• -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci )alkyl, (C3-6)cycloalkyl wherein the (C3- 6)cycloalkyl optionally contains a ring oxygen atom, (C3-6)cycloalkyl-(Ci-3)alkylene wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom, (Ci- 3)fluoroalkyl, or -NH ₂ ;

• -O-CH2-CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci )alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ;

• -O-CH2-O-CO-R ⁰⁵ , wherein R ⁰⁵ repesents (Ci- ₄ )alkyl or (Ci )alkoxy;

· -0-CH ₂ -CH ₂ -N[(Ci )alkyl] ₂ (especially -0-CH ₂ -CH ₂ -N(CH ₃ )2); or

• (5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-O-CH3, -CO-0-C ₂ H ₅ , -0-CH ₂ -COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ - COOH, -NH-CH ₂ -CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ - C(CH ₃ ) ₂ , -CO-NH-S0 ₂ -cyclopropyl, -CO-NH-S0 ₂ -C ₂ H ₅ , -CO-NH-S0 ₂ -NH ₂ , -CO-0-CH ₂ -

COOH, -CO-0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ , -CO-0-CH ₂ -CO-N(CH ₃ ) ₂ , -CO-0-CH ₂ -0-CO-0-C ₂ H ₅ , - CO-0-CH ₂ -0-CO-propyl, (5-methyl-2-oxo-[1 ,3]dioxol -yl)-methyl-0-CO-, -CH ₂ -COOH, - CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , -CH ₂ -CH ₂ -COOH, -CH=CH-COOH, -CH≡CH-CO-0- C ₂ H ₅ , -CF ₂ -COOH, -NH-CO-COOH, -CO-COOH, 1 -carboxy-cyclopropan-1 -yl]; · -CO-CH ₂ -OH;

N ^0H

' NH ₂ .

2-hydroxy-3,4-dioxo-cyclobut-1-enyl;

hydroxy-(Ci )alkyl (especially hydroxymethyl, 1-hydroxy-ethyl);

dihydroxy-(C ₂ -4)alkyl (especially 1 ,2-dihydroxyethyl);

· hydroxy-(C ₂ )alkoxy (especially 2-hydroxy-ethoxy);

(Ci-4)alkoxy-(C ₂ -4)alkoxy (especially 2-methoxy-ethoxy);

-(CH ₂ )rCO-NR ^N3 R ^N4 wherein r represents the integer 0 or 1 ; and wherein R ^N3 and R ⁴ independently represent hydrogen, hydroxy-(C ₂ )alkyl, (Ci- ₃ )alkoxy-(C ₂ -4)alkyl, or hydroxy (wherein preferably at least one of R ^N3 and R ^N4 represents hydrogen; and wherein particular examples of such group -CO-NR ³ R ⁴ are -CO-NH ₂ , -CO-NH(CH ₃ ), -CO-NH(C ₂ H ₅ ), -CH ₂ -CO-NH ₂ , -CO-NH-C ₂ H ₄ -

OH, -CO-NH-C ₂ H ₄ -OCH ₃ , or-CO-N(CH ₃ ) ₂ , -CO-NH-isopropyl, or-CO-NH-OH);

• -X ² -NR ^N1 R ^N2 , wherein X ² represents -(CH ₂ ) _m -, wherein m represents the integer 0 or 1; or X ² represents -0-CH ₂ -CH ₂ - ^* ,wherein the asterisk indicates the bond that is linked to the -NR ^N1 R ^N2 group; and wherein

■ R ^N1 and R ^N2 independently represent hydrogen, (Ci- ₄ )alkoxy-(C ₂ )alkyl, (C ₃ .

6)cycloalkyl, or (C ₂ . ₃ )fluoroalkyl;

■ or R ^N1 independently represents hydrogen or (Ci-4)alkyl, and R ² independently represents -CO-H, -CO-(Ci- ₃ )alkyl, -CO-(Ci. ₃ )alkylene-OH, or -CO-0-(Ci. ₃ )alkyl; ^■ or R ^N1 and R ² together with the nitrogen to which they are attached form a 4-, 5- or 6- membered saturated ring optionally containing one ring oxygen or ring sulfur atom, wherein said ring is unsubstituted, or mono-substituted with oxo on a ring carbon atom, or disubstituted with oxo on a ring sulfur atom;

(especially such group -X ² -NR ^N1 R ^N2 represents amino, methylamino, ethylamino, propylamino, amino-methyl, methylamino-methyl, isobutylamino-methyl, cyclopropylamino-methyl, cyclobutylamino-methyl, (2-methoxyethyl)amino-methyl, (2,2,2-trifluoro-ethyl)-amino; or -NH- CO-H, -N(C ₂ H ₅ )-CO-H, -NH-CO-C2H5, -NH-CO-CH2-CH2-OH, -NH-CO-O-CH3, -N(CH ₃ )-CO-0- CH3; or pyrrolidin-1-yl, 2-oxo-pyrrolidin-1-yl, 1 ,1 -dioxo-isothiazolidin-2-yl, morpholin-4-yl, azetidin-1-yl, or piperidin-1-yl; or 2-(dimethylamino)-ethoxy);

-NH-CO-NR ^N5 R ^N6 wherein R ^N5 and R ⁶ independently represent hydrogen or (Ci-4)alkyl (wherein preferably at least one of R ⁵ and R ⁶ represents hydrogen; and wherein particular examples of such group -NH-CO-NR ⁵ R ⁶ are -NH-CO-NH2, -NH-CO-NH-C2H5);

-S02-R ^S1 wherein R ^S1 represents hydroxy, (Ci-4)alkyl (especially methyl), or -NR ^N7 R ^N8 wherein R ^N7 and R ^N8 independently represent hydrogen or (Ci-3)alkyl (wherein preferably at least one of R ^N7 and R ⁸ represents hydrogen; and wherein particular examples of such group -S02-R ^S1 are -SO2-CH3, - SO2-NH2, -SO2-OH, -SO2-NH-CH3);

-S-R ^S2 wherein R ^S2 represents (Ci-4)alkyl (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); -(CH2)q-HET ¹ , wherein q represents the integer 0, 1 or 2 (especially q is 0, i.e. HET ¹ is linked to Ar ¹ by a direct bond); and wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl), 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2,4]oxadiazol-5-yl), or 5-thioxo- 4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-mercapto-[1 ,2,4]oxadiazol-3- yi);

-(CH ₂ ) _P -HET, wherein p represents the integer 0 or 1 (especially p is 0, i.e. HET is linked to Ar ¹ by a direct bond); and wherein HET represents a 5- or 6-membered heteroaryl (especially 5-membered heteroaryl selected from oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, and tetrazolyl), wherein said 5- or 6-membered heteroaryl is unsubstituted, or mono- or di-substituted, wherein the substituents are independently selected from (Ci-4)alkyl (especially methyl), (Ci )alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3-s)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or -NR ^N9 R ^N10 wherein R ^N9 and R ^N1 ° independently represent hydrogen, (Ci- 3)alkyl (especially methyl), or (especially 2-hydroxy-ethyl); (especially such group -(CH2)p-HET is 1 H-tetrazol-5-yl, 3-hydroxy-isoxazol-5-yl, 2-hydroxy-[1 ,3,4]oxadiazol-4-yl, 3-amino- isoxazol-5-yl, 2-amino-oxazol-5-yl, 5-amino-[1 ,3,4]thiadiazol-2-yl, 5-methylamino-[1 ,3,4]thiadiazol-2- yl, 5-methoxy-[1 ,2,4]oxadiazol-3-yl, 5-amino-[1 ,2,4]oxadiazol-3-yl, 5-[(2-hydroxy-ethyl)]-amino)- [1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5-(oxetan-3-yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, 2,5-dimethyl-1 H-imidazol-4-yl)

or Ar ¹ represents 8- to 10-membered bicyclic heteroaryl (notably 9- or 10-membered bicyclic heteroaryl; especially indazolyl, benzoimidazolyl, indolyl, benzotriazolyl, benzofuranyl, benzooxazolyl, quinoxalinyl, isoquinolinyl, quinolinyl, pyrrolopyridinyl, or imidazopyridinyl); wherein said 8- to 10-membered bicyclic heteroaryl independently is unsubstituted, mono-, or di-substituted, wherein the substituents are independently selected from (especially methyl); (Ci )alkoxy (especially methoxy); (Ci-3)fluoroalkyl (especially trifluoromethyl); (Ci-3)fluoroalkoxy (especially trifluoromethoxy); halogen; cyano; hydroxy, or -(Co-3)alkylene- COOR ⁰² wherein R ⁰² repesents hydrogen or (Ci-4)alkyl (especially such group -(Co-3)alkylene-COOR ⁰² is - COOH); (especially such 8- to 10-membered bicyclic heteroaryl, if unsubstituted, is 1 H-benzoimidazol-5-yl, 1 H-indol-6-yl, 1 H-indol-5-yl, 1 H-indol-2-yl, 1 H-indazol-5-yl, isoquinolin-7-yl, quinolin-6-yl; or, if substituted, is 3- carboxy-1 H-indol-6-yl, 4-carboxy-1 H-indol-2-yl, 5-carboxy-1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy- 1 H-indol-2-yl, 5-(methoxycarbonyl)-1 H-indol-2-yl, 6-(methoxycarbonyl)-1 H-indol-2-yl), 6-carboxy-benzofuran- 2-yl, 3-carboxy-benzofuran-6-yl, 2-carboxy-benzofuran-5-yl, or 2-carboxy-benzofuran-6-yl);

or Ar ¹ represents a group of the structure (Ar-lll):

(Ar-lll)

wherein ring (B) represents a non-aromatic 5- or 6-membered ring fused to the phenyl group, wherein ring (B) comprises one or two heteroatoms independently selected from nitrogen and oxygen (notably such group (Ar- lll) is 2,3-dihydro-benzofuranyl, 2,3-dihydro-1 H-indolyl, 2,3-dihydro-benzo[1 ,4]dioxinyl, 2,3-dihydro-1 H- indazolyl, 2,3-dihydro-1 H-benzo[d]imidazolyl, 2,3-dihydrobenzo[d]isoxazolyl, 2,3-dihydro-isoindolyl, 2,3- dihydro-benzooxazolyl, 1 ,2,3,4-tetrahydro-quinazolinyl, 1 ,2,3,4-tetrahydro-isoquinolinyl, or 1 ,2,3,4-tetrahydro- phthalazinyl); wherein said ring (B) independently is unsubstituted, mono-, or di-substituted, wherein the substituents are independently selected from oxo, (Ci-e)alkyl (especially methyl, ethyl, propyl, butyl, isobutyl) and -(Co-3)alkylene-COOR ⁰³ wherein R ⁰³ repesents hydrogen or (Ci-3)alkyl (especially such group (Ar-lll) is 2- oxo-2,3-dihydro-benzooxazol-6-yl, 3-methyl-2-oxo-2,3-dihydro-benzooxazol-5-yl, 1 -methyl-3-oxo-2 ,3-d i hydro- 1 H-indazol-6-yl, 2-oxo-1 ,2,3,4-tetrahydro-quinazolin-6-yl, 1-methyl-2-oxo-1 ,2,3,4-tetrahydro-quinazolin-6-yl, 1- oxo-1 , 2,3,4-tetrahydro-isoquinolin-6-yl, 1-methyl-2-oxo-1 ,2,3,4-tetrahydro-quinazolin-7-yl, or 1-oxo-1 , 2,3,4- tetrahydro-isoquinolin-7-yl). In a sub-embodiment, Ar ¹ especially represents

• phenyl, or 5- or 6-membered heteroaryl; wherein said phenyl or 5- or 6-membered heteroaryl independently is mono-, di- or tri-substituted (especially di-substituted),

^■ wherein one of said substituents is selected from (C^cycloalkyl containing a ring oxygen atom, wherein said containing a ring oxygen atom is unsubstituted or mono-substituted with

hydroxy; hydroxy; ;-X -CO-R ⁰¹ ; 2-hyd roxy-3 ,4-d i oxo-cycl ob ut- 1 -enyl ; hydroxy-(C )alkoxy; -(CH ₂ )rCO-NR ^N3 R ^N4 ; -NH-CO-NR ⁵ R ⁶ ; -S0 ₂ -R ^S1 ; -(CH ₂ ) _q -HET ¹ ; -(CH ₂ ) _P -HET;

• and the other of said substituents, if present, independently are selected from (Ci )alkyl; (Ci )alkoxy;

(Ci )fluoroalkyl; (Ci )fluoroalkoxy; halogen; cyano; (C3 )cycloalkyl, wherein said (C3 )cycloalkyl is unsubstituted or mono-substituted with amino; (C3 )cycloalkyl-oxy; hydroxy; hydroxy-(Ci )alkyl; dihydroxy-(C ₂ . ₄ )alkyl; hydroxy-(C )alkoxy; (Ci- ₄ )alkoxy-(C )alkoxy; -X ² -NR ¹ R ² ; -S-R ^S2 ; wherein the above groups and substituents are as defined in embodiment 1 ).

• or Ar ¹ represents 8- to 10-membered bicyclic heteroaryl as defined in embodiment 1 ); wherein said 8- to 10- membered bicyclic heteroaryl independently is unsubstituted, mono-, or di-substituted, wherein the substituents are independently selected from (Ci )alkoxy; (Ci )fluoroalkyl; (Ci )fluoroalkoxy; halogen; cyano; hydroxy, or -(Co )alkylene-COOR ⁰² wherein R ⁰² repesents hydrogen or

• or Ar ¹ represents a group of the structure (Ar-lll) as defined in embodiment 1 ).

2) A second embodiment relates to compounds according to embodiment 1 ), wherein R ³ represents hydrogen.

3) Another embodiment relates to compounds according to embodiment 1 ), wherein R ³ represents methyl. 4) Another embodiment relates to compounds according to any one of embodiments 1 ) to 3), wherein R ^4a and R ^4b both represent hydrogen.

5) Another embodiment relates to compounds according to any one of embodiments 1 ) to 4), wherein R ^5a and R ^5b both represent hydrogen. Particular compounds of formula (I) are compounds wherein R ^4a and R ^4b both represent hydrogen; and R ^5a and R ^5b both represent hydrogen.

6) Another embodiment relates to compounds according to any one of embodiments 1 ) to 5), wherein the characteristics defined for the fragment

according to embodiments 8), and 15) to 25) below apply mutatis mutandis.

7) Another embodiment relates to compounds according to any one of embodiments 1 ) to 6), wherein the characteristics defined for the substituent Ar ¹ according to embodiments 8) to 14) below apply mutatis mutandis.

8) A second aspect of the invention relates to compounds of the formula (II)

is substituted with R ² , wherein R ² represents hydrogen, (especially methyl, ethyl), halogen (especially chloro, bromo), or cyano; and

is optionally substituted with (R ¹ ) _n ; wherein (R ¹ ) _n represents one, two or three optional substituents (i.e. said fragment is, in addtition to R ² , unsubstituted, or substituted with one, two or three R ¹ ), wherein said substituents R ¹ are independently selected from (Ci-3)alkyl (especially methyl), (Ci-3)alkoxy (especially methoxy), halogen (especially fluoro, or chloro), (Ci-3)fluoroalkyl (especially trifluoromethyl), (Ci-3)fluoroalkoxy (especially trifluoromethoxy), or cyano; (for avoidance of any doubt: substituents (R ¹ ) _n are in addition to the substituent R ² as defined above);

X represents S or 0; Ar ¹ represents

• a phenyl group of the structure (Ar-I):

(Ar-I)

wherein

R ^p represents

-6)cycloalkyl containing a ring oxygen atom, wherein said -6)cycloalkyl containing a ring oxygen atom is unsubstituted or mono-substituted with hydroxy (especially 3-hydroxy-oxetan-3-yl);

> hydroxy;

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci. ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH ₂ - CH ₂ -), -0-(Ci. ₃ )alkylene-* (especially -0-CH ₂ -*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci. ₃ )alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -S-CH ₂ -*, -CF ₂ - -CH=CH-, - CH≡CH-, -NH-CO-*, -CO-, or (C ₃ -5)cycloalkylene; wherein the asterisks indicate the bond that is linked to the -CO-R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci )alkyl, (C ₃ -6)cycloalkyl wherein the (C ₃ .

6)cycloalkyl optionally contains a ring oxygen atom, (C ₃ -6)cycloalkyl-(Ci- ₃ )alkylene wherein the (C ₃ -6)cycloalkyl optionally contains a ring oxygen atom, (Ci- 3)fluoroalkyl, or -NH ₂ ;

^■ -0-CH ₂ -CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci )alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ;

^■ -0-CH ₂ -0-CO-R ⁰⁵ , wherein R ⁰⁵ repesents (Ci- ₄ )alkyl or (Ci )alkoxy;

^■ -0-CH ₂ -CH ₂ -N[(Ci )alkyl] ₂ (especially -0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ ); or

^■ (5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-0-CH ₃ , -CO-0-C ₂ H ₅ , -0- CH ₂ -COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ -COOH, - NH-CH ₂ -CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH- S0 ₂ -cyclopropyl, -CO-NH-S0 ₂ -C ₂ H ₅ , -CO-NH-S0 ₂ -NH ₂ , -CO-0-CH ₂ -COOH, -CO-0-CH ₂ -CH ₂ - N(CH ₃ ) ₂ , -CO-0-CH ₂ -CO-N(CH ₃ ) ₂ , -CO-0-CH ₂ -0-CO-0-C ₂ H ₅ , -CO-0-CH ₂ -0-CO-propyl, (5- methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyl-0-CO-, -CH ₂ -COOH, -CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , - CH2-CH2-COOH, -CH=CH-C00H, -CH≡CH-CO-0-C ₂ H ₅ , -CF2-COOH, -NH-C0-C00H, -CO- COOH , 1 -carboxy-cyclopropan-1 -yl];

> 2-hydroxy-3,4-dioxo-cyclobut-1-enyl;

> hydroxy-(Ci )alkyl (especially hydroxymethyl, 1-hydroxy-ethyl);

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy);

> -(CH ₂ )rCO-NR ^N3 R ^N4 wherein r represents the integer 0 or 1 ; and wherein R ^N3 and R ⁴ independently represent hydrogen, hydroxy-(C2 )alkyl, (Ci-3)alkoxy-(C2-4)alkyl, or hydroxy (wherein preferably at least one of R ³ and R ⁴ represents hydrogen; and wherein particular examples of such group -CO-NR ³ R ⁴ are -CO-NH2, -CO-NH(CH ₃ ), -CO-NH(C ₂ H ₅ ), -CH2-CO-NH2, -CO-NH-C2H4-

OH, -CO-NH-C2H4-OCH3, or -CO-N(CH ₃ ) ₂ , -CO-NH-isopropyl, or -CO-NH-OH);

> -NR ^N1 R ^N2 , wherein R ^N1 independently represents hydrogen or (Ci-4)alkyl, and R ^N2 independently represents -CO-H, -CO-(Ci-3)alkyl, or -CO-(Ci-3)alkylene-OH; (especially such group -(CH2) _m - N _R Ni _R N2 represents-NH-CO-H, -N(C ₂ H ₅ )-CO-H, -NH-CO-C2H5, or -NH-CO-CH2-CH2-OH);

> -NH-CO-NR ^N5 R ^N6 wherein R ^N5 and R ⁶ independently represent hydrogen or (wherein preferably at least one of R ⁵ and R ⁶ represents hydrogen; and wherein particular examples of such group -NH-CO-NR ⁵ R ⁶ are -NH-CO-NH2, -NH-CO-NH-C2H5);

> -S0 ₂ -R ^S1 wherein R ^S1 represents (especially methyl), or -NR ^N7 R ^N8 wherein R ^N7 and R ^N8 independently represent hydrogen or (Ci-3)alkyl (wherein preferably at least one of R ⁷ and R ⁸ represents hydrogen; and wherein particular examples of such group -S02-R ^S1 are -SO2-CH3, -SO2-

-(CH2)q-HET ¹ , wherein q represents the integer 0, 1 or 2 (especially q is 0, i.e. HET ¹ is linked to Ar ¹ by a direct bond); and wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl), 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2,4]oxadiazol-5-yl), or 5-thioxo-

4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-mercapto-[1 ,2,4]oxadiazol-3- yi);

> -(CH ₂ ) _P -HET, wherein p represents the integer 0 or 1 (especially p is 0, i.e. HET is linked to Ar ¹ by a direct bond); and wherein HET represents a 5-membered heteroaryl (especially oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl), wherein said 5-membered heteroaryl is unsubstituted, or mono- or di-substituted, wherein the substituents are independently selected from (especially methyl), (Ci-4)alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3-s)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or -NR ^N9 R ^N10 wherein R ^N9 and R ¹ ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or hydroxy-(C2 )alkyl (especially 2-hydroxy-ethyl); (especially such group -(CH ₂ ) _P -HET is 1 H-tetrazol-5-yl, 3-hyd roxy-i soxazol -5-y 1 , 2-hydroxy- [1,3,4]oxadiazol-4-yl, 3-amino-isoxazol-5-yl, 2-amino-oxazol-5-yl, 5-amino-[1 ,3,4]thiadiazol-2-yl, 5- methylamino-[1 ,3,4]thiadiazol-2-yl, 5-methoxy-[1 ,2,4]oxadiazol-3-yl, 5-amino-[1 ,2,4]oxadiazol-3-yl, 5- [(2-hydroxy-ethyl)]-amino)-[1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5-(oxetan-3- yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, 2,5-dimethyl-1 H-imidazol-4-yl);

R ^m1 represents

> hydrogen;

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl);

> (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> (C3-6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy;

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy);

> -X ² -NR ^N1 R ^N2 , wherein X ² represents a direkt bond; or X ² represents -O-CH2-CH2-*, wherein the asterisk indicates the bond that is linked to the -NR ^N1 R ^N2 group; and wherein R ^N1 and R ^N2 independently represent hydrogen, (especially methyl), or (C3-6)cycloalkyl (especially cyclopropyl); (especially such group -X ² -NR ^N1 R ^N2 represents amino, methylamino, ethylamino, propylamino; or 2-(dimethylamino)-ethoxy);

> -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); wherein in a sub-embodiment, R ^m1 especially is different from hydrogen;

R ^m2 represents hydrogen, methyl, fluoro, or chloro; and

R ⁰¹ represents hydrogen; or, in case R ^m2 represents hydrogen, R ⁰¹ represents hydrogen or fluoro; Ar ¹ represents a 5-membered heteroaryl group of the structure (Ar-ll):

(Ar-ll)

wherein Y represents CR ⁸ wherein R ⁸ represents especially hydrogen, or halogen (notably fluoro, chloro); or Y represents N;

R ⁷ represents

> (C4-6)cycloalkyl containing a ring oxygen atom, wherein said (C4-6)cycloalkyl containing a ring oxygen atom is unsubstituted or mono-substituted with hydroxy (especially 3-hydroxy-oxetan-3-yl);

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci. ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH2-CH2-), -0-(Ci. ₃ )alkylene-* (especially -O-CH2-*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci- 3)alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -S-CH ₂ -*, -CF ₂ - -CH=CH-, -CH≡CH-, -NH- CO-*, -CO-, or (C ₃ -5)cycloalkylene; wherein the asterisks indicate the bond that is linked to the - CO-R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci-4)alkyl, (C ₃ -6)cycloalkyl wherein the (C ₃ .

6)cycloalkyl optionally contains a ring oxygen atom, (C ₃ -6)cycloalkyl-(Ci- ₃ )alkylene wherein the (C ₃ -6)cycloalkyl optionally contains a ring oxygen atom, (Ci- ₃ )fluoroalkyl, or -NH ₂ ;

^■ -0-CH ₂ -CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci- ₄ )alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ;

^■ -0-CH ₂ -0-CO-R ⁰⁵ , wherein R ⁰⁵ repesents or (Ci- ₄ )alkoxy; or

^■ -0-CH ₂ -CH ₂ -N[(Ci. ₄ )alkyl] ₂ (especially -0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ );

^■ (5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-0-CH ₃ , -CO-0-C ₂ H ₅ , -O-CH2- COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ -COOH, -NH-CH ₂ - CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH-S0 ₂ - cyclopropyl, -CO-NH-S0 ₂ -C ₂ H ₅ , -CO-NH-S0 ₂ -NH ₂ , -CO-0-CH ₂ -COOH, -CO-0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ , - CO-0-CH ₂ -CO-N(CH ₃ ) ₂ , -CO-0-CH ₂ -0-CO-0-C ₂ H ₅ , -CO-0-CH ₂ -0-CO-propyl, (5-methyl-2-oxo- [1 ,3]dioxol-4-yl)-methyl-0-CO-, -CH ₂ -COOH, -CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , -CH ₂ -CH ₂ -COOH, - CH=CH-COOH, -CH≡CH-CO-0-C ₂ H ₅ , -CF ₂ -COOH, -NH-CO-COOH, -CO-COOH, 1-carboxy- cyclopropan-1-yl];

> 2-hydroxy-3,4-dioxo-cyclobut-1-enyl;

> hydroxy-(Ci )alkyl (especially hydroxymethyl, 1-hydroxy-ethyl);

> hydroxy-(C ₂ )alkoxy (especially 2-hydroxy-ethoxy); > -(CH ₂ )rCO-NR ^N3 R ^N4 wherein r represents the integer 0 or 1 ; and wherein R ^N3 and R ⁴ independently represent hydrogen, hydroxy-(C ₂ )alkyl, (Ci-3)alkoxy-(C2-4)alkyl, or hydroxy (wherein preferably at least one of R ³ and R ⁴ represents hydrogen; and wherein particular examples of such group -CO-NR ³ R ⁴ are -CO-NH ₂ , -CO-NH(CH ₃ ), -CO-NH(C ₂ H ₅ ), -CH ₂ -CO-NH ₂ , -CO-NH-C ₂ H ₄ - OH, -CO-NH-C ₂ H ₄ -OCH ₃ , or -CO-N(CH ₃ ) ₂ , -CO-NH-isopropyl, or -CO-NH-OH);

> -NR ^N1 R ^N2 , wherein R ^N1 independently represents hydrogen or (Ci-4)alkyl, and R ² independently represents -CO-H, -CO-(Ci-3)alkyl, or -CO-(Ci-3)alkylene-OH; (especially such group -(CH ₂ ) _m - NRMRN2 represents-NH-CO-H, -N(C ₂ H ₅ )-CO-H, -NH-CO-C ₂ H ₅ , or -NH-CO-CH ₂ -CH ₂ -OH);

> -NH-CO-NR ^N5 R ^N6 wherein R ^N5 and R ⁶ independently represent hydrogen or (wherein preferably at least one of R ⁵ and R ⁶ represents hydrogen; and wherein particular examples of such group -NH-CO-NR ⁵ R ⁶ are -NH-CO-NH ₂ , -NH-CO-NH-C ₂ H ₅ );

> -S0 ₂ -R ^S1 wherein R ^S1 represents (especially methyl), or -NR ^N7 R ^N8 wherein R ^N7 and R ^N8 independently represent hydrogen or (Ci-3)alkyl (wherein preferably at least one of R ⁷ and R ⁸ represents hydrogen; and wherein particular examples of such group -S0 ₂ -R ^S1 are -S0 ₂ -CH ₃ , -S0 ₂ - NH ₂ , -S0 ₂ -NH-CH ₃ );

-(CH ₂ )q-HET ¹ , wherein q represents the integer 0, 1 or 2 (especially q is 0, i.e. HET ¹ is linked to Ar ¹ by a direct bond); and wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl), 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2,4]oxadiazol-5-yl), or 5-thioxo- 4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-mercapto-[1 ,2,4]oxadiazol-3- yi);

> -(CH ₂ ) _P -HET, wherein p represents the integer 0 or 1 (especially p is 0, i.e. HET is linked to Ar ¹ by a direct bond); and wherein HET represents a 5-membered heteroaryl (especially oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl), wherein said 5-membered heteroaryl is unsubstituted, or mono- or di-substituted, wherein the substituents are independently selected from (especially methyl), (Ci )alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3-5)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or -NR ^N9 R ^N10 wherein R ^N9 and R ¹ ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or hydroxy-(C ₂ )alkyl (especially 2-hydroxy-ethyl); (especially such group -(CH ₂ ) _P -HET is 1 H-tetrazol-5-yl , 3-hydroxy-isoxazol-5-yl, 2-hydroxy- [1 ,3,4]oxadiazol-4-yl, 3-amino-isoxazol-5-yl, 2-amino-oxazol-5-yl, 5-amino-[1 ,3,4]thiadiazol-2-yl, 5- methylamino-[1 ,3,4]thiadiazol-2-yl, 5-methoxy-[1 ,2,4]oxadiazol-3-yl, 5-amino-[1 ,2,4]oxadiazol-3-yl, 5- [(2-hydroxy-ethyl)]-amino)-[1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5-(oxetan-3- yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, 2,5-dimethyl-1 H-imidazol-4-yl); R ⁶ represents

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl); > (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> hydroxy;

> (C3-6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy);

> -X ² -NR ^N1 R ^N2 , wherein X ² represents a direkt bond; or X ² represents -O-CH2-CH2-*, wherein the asterisk indicates the bond that is linked to the -NR ^N1 R ^N2 group; and wherein R ^N1 and R ² independently represent hydrogen, or (C3-6)cycloalkyl; (especially such group -X ² -NR ^N1 R ^N2 represents amino, methylamino, ethylamino, propylamino; or 2-(dimethylamino)-ethoxy);

> -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); · or Ar ¹ represents 8- to 10-membered bicyclic heteroaryl (notably 9- or 10-membered bicyclic heteroaryl; especially indazolyl, benzoimidazolyl, indolyl, benzofuranyl, benzooxazolyl, quinoxalinyl, isoquinolinyl, or quinolinyl); wherein said 8- to 10-membered bicyclic heteroaryl independently is mono-substituted with -(Co- 3)alkylene-COOR ⁰² wherein R ⁰² repesents hydrogen or (Ci-4)alkyl (especially methyl) (wherein especially such group -(Co-3)alkylene-COOR ⁰² is -COOH); (especially such 8- to 10-membered bicyclic heteroaryl is 3-carboxy- 1 H-indol-6-yl, 4-carboxy-1 H-indol-2-yl, 5-carboxy-1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol-

2-yl, 5-(methoxycarbonyl)-1 H-indol-2-yl, 6-(methoxycarbonyl)-1 H-indol-2-yl), 6-carboxy-benzofuran-2-yl, 3- carboxy-benzofuran-6-yl, 2-carboxy-benzofuran-5-yl, or 2-carboxy-benzofuran-6-yl);

• or Ar ¹ represents a group of the structure (Ar-lll):

(Ar-lll)

which is selected from 2-oxo-2,3-dihydro-benzooxazol-6-yl, 3-methyl-2-oxo-2,3-dihydro-benzooxazol-5-yl, 1- methyl-3-oxo-2,3-dihydro-1 H-indazol-6-yl, 2-oxo-1 ,2,3,4-tetrahydro-quinazolin-6-yl, 1 -methyl-2-oxo-1 , 2,3,4- tetrahydro-quinazolin-6-yl, 1 -oxo-l ,2,3,4-tetrahydro-isoquinolin-6-yl, 1 -methyl-2-oxo-1 ,2,3,4-tetrahydro- quinazolin-7-yl, and 1 -oxo-l ,2,3,4-tetrahydro-isoquinolin-7-yl.

The compounds of formula (I) / formula (II) may contain one or more stereogenic or asymmetric centers, such as one or more asymmetric carbon atoms, which are allowed to be present in (R)- as well as (S)-configuration. The compounds of formula (I) / formula (II) may further encompass compounds with one or more double bonds which are allowed to be present in Z- as well as E-configuration and/or compounds with substituents at a ring system which are allowed to be present, relative to each other, in cis- as well as trans-configuration. The compounds of formula (I) / formula (II) may thus be present as mixtures of stereoisomers or preferably as pure stereoisomers. Mixtures of stereoisomers may be separated in a manner known to a person skilled in the art.

In case a particular compound (or generic structure) is designated as (R)- or (S)-enantiomer, such designation is to be understood as referring to the respective compound (or generic structure) in enriched, especially essentially pure, enantiomeric form. Likewise, in case a specific asymmetric center in a compound is designated as being in (R)- or (S)-configuration or as being in a certain relative configuration, such designation is to be understood as referring to the compound that is in enriched, especially essentially pure, form with regard to the respective configuration of said asymmetric center. In analogy, cis- or irans-designations are to be understood as referring to the respective stereoisomer of the respective relative configuration in enriched, especially essentially pure, form. Likewise, in case a particular compound (or generic structure) is designated as Z- or E-stereoisomer (or in case a specific double bond in a compound is designated as being in Z- or E-configuration), such designation is to be understood as referring to the respective compound (or generic structure) in enriched, especially essentially pure, stereoisomeric form (or to the compound that is in enriched, especially essentially pure, form with regard to the respective configuration of the double bond).

The term "enriched", when used in the context of stereoisomers, is to be understood in the context of the present invention to mean that the respective stereoisomer is present in a ratio of at least 70:30, especially of at least 90:10 (i.e., in a purity of at least 70% by weight, especially of at least 90% by weight), with regard to the respective other stereoisomer / the entirety of the respective other stereoisomers.

The term "essentially pure", when used in the context of stereoisomers, is to be understood in the context of the present invention to mean that the respective stereoisomer is present in a purity of at least 95% by weight, especially of at least 99% by weight, with regard to the respective other stereoisomer / the entirety of the respective other stereoisomers.

The present invention also includes isotopically labelled, especially ² H (deuterium) labelled compounds of formula (I) / formula (II) according to embodiments 1 ) to 34), which compounds are identical to the compounds of formula (I) / formula (II) except that one or more atoms have each been replaced by an atom having the same atomic number but an atomic mass different from the atomic mass usually found in nature. Isotopically labelled, especially ² H (deuterium) labelled compounds of formula (I) / formula (II) and salts thereof are within the scope of the present invention. Substitution of hydrogen with the heavier isotope ² H (deuterium) may lead to greater metabolic stability, resulting e.g. in increased in-vivo half-life or reduced dosage requirements, or may lead to reduced inhibition of cytochrome P450 enzymes, resulting e.g. in an improved safety profile. In one embodiment of the invention, the compounds of formula (I) / formula (II) are not isotopically labelled, or they are labelled only with one or more deuterium atoms. In a sub-embodiment, the compounds of formula (I) / formula (II) are not isotopically labelled at all. Isotopically labelled compounds of formula (I) /formula (II) may be prepared in analogy to the methods described hereinafter, but using the appropriate isotopic variation of suitable reagents or starting materials.

In this patent application, a bond drawn as a dotted line shows the point of attachment of the radical drawn. For example, the radical drawn below

is the 2-methyl-1 - -indol-1 -yl group.

In some instances, the compounds of formula (I) / formula (II) may contain tautomeric forms. Such tautomeric forms are encompassed in the scope of the present invention. In case tautomeric forms exist of a certain residue, and only one form of such residue is disclosed or defined, the other tautomeric form(s) are understood to be encompassed in such disclosed residue. For example the group 2-oxo-2 ,3-d i hyd ro- 1 H-benzo[d]imidazol-5-yl is to be understood as also encompassing its tautomeric forms 2-hydroxy-1 H-benzo[d]imidazol-5-yl and 2-hydroxy-3H- benzo[d]imidazol-5-yl. Similarly, 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (alternatively named 5-oxo-4H- [1 ,2,4]oxadiazol-3-yl) encompasses its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl, and 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (alternatively named 3-oxo-2H-[1 ,2,4]oxadiazol-5-yl) encompasses its tautomeric form 3- hydroxy-[1 ,2,4]oxadiazol-5-yl.

Where the plural form is used for compounds, salts, pharmaceutical compositions, diseases and the like, this is intended to mean also a single compound, salt, or the like.

Any reference to compounds of formula (I) / formula (II) according to embodiments 1 ) to 34) is to be understood as referring also to the salts (and especially the pharmaceutically acceptable salts) of such compounds, as appropriate and expedient.

The term "pharmaceutically acceptable salts" refers to salts that retain the desired biological activity of the subject compound and exhibit minimal undesired toxicological effects. Such salts include inorganic or organic acid and/or base addition salts depending on the presence of basic and/or acidic groups in the subject compound. For reference see for example "Handbook of Phramaceutical Salts. Properties, Selection and Use.", P. Heinrich Stahl, Camille G. Wermuth (Eds.), Wiley-VCH, 2008; and "Pharmaceutical Salts and Co-crystals", Johan Wouters and Luc Quere (Eds.), RSC Publishing, 2012.

Definitions provided herein are intended to apply uniformly to the compounds of formula (I) / formula (II), as defined in any one of embodiments 1 ) to 25), and, mutatis mutandis, throughout the description and the claims unless an otherwise expressly set out definition provides a broader or narrower definition. It is well understood that a definition or preferred definition of a term defines and may replace the respective term independently of (and in combination with) any definition or preferred definition of any or all other terms as defined herein. Whenever the group Ar ¹ or substituents thereof are further defined, such definitions are intended to apply mutatis mutandis also to the groups (Ar-I), (Ar-ll), and (Ar-lll) and their respective substituents.

Whenever a substituent is denoted as optional, it is understood that such substituent may be absent (i.e. the respective residue is unsubstituted with regard to such optional substituent), in which case all positions having a free valency (to which such optional substituent could have been attached to; such as for example in an aromatic ring the ring carbon atoms and / or the ring nitrogen atoms having a free valency) are substituted with hydrogen where appropriate. Likewise, in case the term "optionally" is used in the context of (ring) heteroatom(s), the term means that either the respective optional heteroatom(s), or the like, are absent (i.e. a certain moiety does not contain heteroatom(s) / is a carbocycle / or the like), or the respective optional heteroatom(s), or the like, are present as explicitly defined.

The term "halogen" means fluorine, chlorine, bromine, or iodine; especially fluorine, chlorine, or bromine; preferably fluorine or chlorine.

The term "alkyl", used alone or in combination, refers to a saturated straight or branched chain hydrocarbon group containing one to six carbon atoms. The term "(C _x - _y )alkyl" (x and y each being an integer), refers to an alkyl group as defined before, containing x to y carbon atoms. For example a (Ci-e)alkyl group contains from one to six carbon atoms. Examples of alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl, 3-methyl-butyl, 2,2- dimethyl-propyl and 3,3-dimethyl-butyl. For avoidance of any doubt, in case a group is referred to as e.g. propyl or butyl, it is meant to be n-propyl, respectively n-butyl. Preferred are methyl and ethyl. Most preferred is methyl. Preferred for substituents of Ar ¹ being phenyl or 5- or 6-membered heteroaryl are methyl, ethyl, propyl, isobutyl, 1- methyl-propan-1 -yl, tert.-butyl, 3-methyl-butyl.

The term "-(C _x-y )alkylene-", used alone or in combination, refers to bivalently bound alkyl group as defined before containing x to y carbon atoms. Preferably, the points of attachment of a -(Ci _-y )alkylene group are in 1 ,1 -diyl, in 1 ,2- diyl, or in 1 ,3-diyl arrangement. In case a (Co-y)alkylene group is used in combination with another substituent, the term means that either said substituent is linked through a (Ci-y)alkylene group to the rest of the molecule, or it is directly attached to the rest of the molecule (i.e. a (Co)alkylene group represents a direct bond linking said substituent to the rest of the molecule). The alkylene group -C2H4- refers to -CH2-CH2- if not explicitly indicated otherwise. For the linker X ¹ , examples of (Ci-3)alkylene groups are -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ )2-, and -CH2-CH2-, especially -CH ₂ - and -CH2-CH2-. Examples of (Co-3)alkylene groups as used in the substituents -(Co-3)alkylene- COOR ⁰² and (Co-3)alkylene-COOR ⁰³ , respectively, are (Co)alkylene, and methylene, respectively.

The term "alkoxy", used alone or in combination, refers to an alkyl-O- group wherein the alkyl group is as defined before. The term "(C _x . _y )alkoxy" (x and y each being an integer) refers to an alkoxy group as defined before containing x to y carbon atoms. For example a (Ci-4)alkoxy group means a group of the formula in which the term "(Ci-4)alkyl" has the previously given significance. Examples of alkoxy groups are methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec.-butoxy and tert.-butoxy. Preferred are ethoxy and especially methoxy. Preferred forsubstituents of Ar ¹ being phenyl or5- or6-membered heteroaryl are methoxy, ethoxy, propoxy, butoxy, isobutoxy.

The term "fluoroalkyl", used alone or in combination, refers to an alkyl group as defined before containing one to three carbon atoms in which one or more (and possibly all) hydrogen atoms have been replaced with fluorine. The term " ( C _x - _y )f I u o roa I ky I" (x and y each being an integer) refers to a fluoroalkyl group as defined before containing x to y carbon atoms. For example a (Ci-3)fluoroalkyl group contains from one to three carbon atoms in which one to seven hydrogen atoms have been replaced with fluorine. Representative examples of fluoroalkyl groups include trifluoromethyl, 2-fluoroethyl, 2,2-difluoroethyl and 2,2,2-trifluoroethyl. Preferred are (Ci)fluoroalkyl groups such as trifluoromethyl. An example of "(Ci-3)fluoroalkyl, wherein said (Ci-3)fluoroalkyl is optionally substituted with hydroxy" is 2,2,2-trifluoro-1-hydroxy-ethyl.

The term "fluoroalkoxy", used alone or in combination, refers to an alkoxy group as defined before containing one to three carbon atoms in which one or more (and possibly all) hydrogen atoms have been replaced with fluorine. The term "(C _x . _y )fluoroalkoxy" (x and y each being an integer) refers to a fluoroalkoxy group as defined before containing x to y carbon atoms. For example a (Ci-3)fluoroalkoxy group contains from one to three carbon atoms in which one to seven hydrogen atoms have been replaced with fluorine. Representative examples of fluoroalkoxy groups include trifluoromethoxy, difluoromethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy and 2,2,2-thfluoroethoxy. Preferred are (Ci)fluoroalkoxy groups such as trifluoromethoxy and difluoromethoxy, as well as 2,2,2- thfluoroethoxy.

The term "cycloalkyl", used alone or in combination, refers to a saturated monocyclic hydrocarbon ring containing three to six carbon atoms. The term "(C _x - _y )cycloalkyl" (x and y each being an integer), refers to a cycloalkyl group as defined before containing x to y carbon atoms. For example a (C3-6)cycloalkyl group contains from three to six carbon atoms. Examples of cycloalkyl groups are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl.

Preferred are cyclopropyl, cyclobutyl, and cyclopentyl; especially cyclopropyl. An example of cycloalkyl groups containing one ring oxygen atom is especially oxetanyl. Examples of (C3-6)cycloalkyl groups wherein said (C3- 6)cycloalkyl is optionally mono-substituted with amino are cyclopropyl, 1-amino-cyclopropyl. Examples of (C3-

6)cycloalkyl groups wherein said (C3-6)cycloalkyl is mono-substituted with-COOH are 1-carboxy-cyclopropyl, 1- carboxy-cyclopentyl.

The term "-(C _x . _y )cycloalkylene-", used alone or in combination, refers to bivalently bound cycloalkyl group as defined before containing x to y carbon atoms. Preferably, the points of attachment of any bivalently bound cycloalkyl group are in 1 ,1-diyl, or in 1 ,2-diyl arrangement. Examples are cyclopropan-1 ,1-diyl, cyclopropan-1 ,2-diyl, and cyclopentan-1 ,1-diyl; preferred is cyclopropan-1 ,1-diyl.

Examples of ( C3-6)cycl oa I kyl -oxy are cyclobutyl-oxy, and cyclopentyl-oxy.

Alkylated amino groups -N[(Ci )alkyl]2 as used in groups -X ¹ -CO-R ⁰¹ , wherein R ⁰¹ represents -O-CH2-CO-R ⁰⁴ , wherein R ⁰⁴ repesents -N[(Ci-4)alkyl]2; or wherein R ⁰¹ represents -0-CH2-CH2-N[(Ci-4)alkyl]2 are such that the two repective groups are independently selected. A preferred example of such amino group

is -N(CH ₃ ) ₂ .

The term "heterocycle", used alone or in combination, and if not explicitly defined in a broader or more narrow way, refers to a saturated monocyclic hydrocarbon ring containing one or two (especially one) ring heteroatoms independently selected from nitrogen, sulfur, and oxygen (especially one nitrogen atom, two nitrogen atoms, one nitrogen atom and one oxygen atom, or one nitrogen atom and one sulfur atom). The term "(C _x . _y )heterocycle" refers to such a heterocycle containing x to y ring atoms. Heterocycles are unsubstituted or substituted as explicitly defined.

A group composed of a "non-aromatic 5- or 6-membered ring fused to the phenyl group, wherein ring (B) comprises one or two heteroatoms independently selected from nitrogen and oxygen " as used for (Ar-lll) refers to phenyl groups which are fused to a (C ₅ -6)heterocycle as defined before. Examples are 2,3-dihydro-benzofuranyl, 2,3- dihydro-1 H-indolyl, 2,3-dihydro-benzo[1 ,4]dioxinyl, 2,3-dihydro-1 H-indazolyl, 2,3-dihydro-1 H-benzo[d]imidazolyl, 2,3-dihydrobenzo[d]isoxazolyl, 2,3-dihydro-isoindolyl, 3-dihydro-benzooxazol-6-yl, 2,3-dihydro-benzooxazol-5-yl, 1 ,2,3,4-tetrahydro-quinazolin-6-yl, 1 ,2,3,4-tetrahydro-quinazolin-7-yl, 1 ,2,3,4-tetrahydro-isoquinolin-6-yl, and 1 ,2,3,4-tetrahydro-phthalazin-6-yl. The above groups are unsubstituted, mono-, or di-substituted, wherein the substituents are independently selected from oxo, (Ci-e)alkyl, and -(Co-3)alkylene-COOR ⁰³ wherein R ⁰³ repesents hydrogen or (Ci-3)alkyl (especially methyl); especially substituents are independently selected from oxo, methyl, ethyl, propyl, butyl, isobutyl, or -COOH; wherein the substituents are attached to the fused 5- or 6-membered non- aromatic ring. Oxo substituents are preferably attached to a ring carbon atom which is in alpha position to a ring nitrogen atom. Preferred examples of such groups are 2,3-dihydro-benzofuranyl, 2,3-dihydro-1 H-indolyl, 2,3- dihydro-benzo[1 ,4]dioxinyl; as well as the oxosubstituted heterocyclyl groups 3-oxo-2,3-dihydro-1 H-indazolyl, 2- oxo-2,3-dihydro-1 H-benzo[d]imidazolyl, 3-oxo-2,3-dihydrobenzo[d]isoxazolyl, 2-oxo-1 ,3-dihydro-indolyl, 1 -oxo-2,3- dihydro-isoindolyl, 2-oxo-2,3-dihydro-benzooxazolyl, 2-oxo-1 ,2,3,4-tetrahydro-quinazolinyl, 1-oxo-1 , 2,3,4- tetrahydro-isoquinolinyl, 1 ,4-dioxo-1 ,2,3,4-tetrahydro-phthalazinyl; wherein the above groups optionally carry one (further) substituent independently selected from (Ci-e)alkyl, and -(Co-3)alkylene-COOR ⁰³ wherein R ⁰³ repesents hydrogen or (Ci-3)alkyl (especially methyl). Particular examples are 2-oxo-2,3-dihydro-benzooxazol-6-yl, 3-methyl- 2-oxo-2,3-dihydro-benzooxazol-5-yl, 1 -methyl-3-oxo-2,3-dihydro-1 H-indazol-6-yl, 2-oxo-1 ,2,3,4-tetrahydro- quinazolin-6-yl, 1 -methyl-2-oxo-1 ,2,3,4-tetrahydro-quinazolin-6-yl, 1 -oxo-1 ,2,3,4-tetrahydro-isoquinolin-6-yl, 1- methyl-2-oxo-1 ,2,3,4-tetrahydro-quinazolin-7-yl, or 1-oxo-1 ,2,3,4-tetrahydro-isoquinolin-7-yl.

For avoidance of doubt, certain groups having tautomeric forms which are considered predominantly non-aromatic, such as for example 2-oxo-2,3-dihydro-1 H-benzo[d]imidazolyl groups, are defined herein as 8- to 10-membered partially aromatic fused bicyclic heterocyclyl groups, even though their corresponding tautomeric form (2-hydroxy- 1 H-benzo[d]imidazolyl) could also be considered as a 8- to 10-membered bicyclic heteroaryl group.

The term "aryl", used alone or in combination, means phenyl or naphthyl, especially phenyl. The above-mentioned aryl groups are unsubstituted or substituted as explicitly defined. Examples of the substituent Ar ¹ representing phenyl are especially those which are at least mono-substituted in para position with respect to the point of attachment of the rest of the molecule. In addition, such group Ar ¹ representing phenyl may carry one or two further substituents, especially in one or both meta positions with respect to the point of attachment of the rest of the molecule. The respective substituents of such phenyl groups are as explicitly defined.

The term "heteroaryl", used alone or in combination, means a 5- to 10-membered monocyclic or bicyclic aromatic ring containing one to a maximum of four heteroatoms, each independently selected from oxygen, nitrogen and sulfur. Examples of such heteroaryl groups are 5-membered heteroaryl groups such as furanyl, oxazolyl, isoxazolyl, oxadiazolyl, thiophenyl, thiazolyl, isothiazolyl, thiadiazolyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl; 6- membered heteroaryl groups such as pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl; and 8- to 10-membered bicyclic heteroaryl groups such as indolyl, isoindolyl, benzofuranyl, isobenzofuranyl, benzothiophenyl, indazolyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, benzoisothiazolyl, benzotriazolyl, benzoxadiazolyl, benzothiadiazolyl, thienopyridinyl, quinolinyl, isoquinolinyl, naphthyridinyl, cinnolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, pyrrolopyridinyl, pyrazolopyridinyl, pyrazolopyrimidinyl, pyrrolopyrazinyl, imidazopyridinyl, imidazopyridazinyl, and imidazothiazolyl. The above-mentioned heteroaryl groups are unsubstituted or substituted as explicitly defined.

For the substituent Ar ¹ representing a "5- or 6-membered heteroaryl", the term means the above-mentioned 5- or 6-membered groups such as especially pyridinyl, pyrimidinyl, pyrrolyl, pyrazolyl, isoxazolyl, thiazolyl or thiophenyl. Notably, the term refers to 5-membered groups such as especially thiazolyl or thiophenyl; in particular thiophen-2- yl, thiophen-3-yl, thiazol-2-yl, thiazol-4-yl, thiazol-5-yl. Preferred is thiophenyl, especially thiophen-2-yl; or thiazolyl, especially thiazol-2-yl. The above groups are substituted as explicitly defined. Thiophen-2-yl or thiazol-2-yl are especially di-substituted with one substituent being in position 5, and a second substituent in position 4 (and, for thiophen-2-yl, optionally a halogen substituent in position 3).

For the substituent Ar ¹ representing a "8- to 10-membered bicyclic heteroaryl" the term means the above-mentioned 8- to 10-membered heteroaryl groups. Notably, the term refers to 9- or 10-membered heteroaryl groups, such as especially indazolyl, benzoimidazolyl, indolyl, benzotriazolyl, benzooxazolyl, quinoxalinyl, isoquinolinyl, quinolinyl, pyrrolopyridinyl, and imidazopyridinyl, as well as benzofuranyl, benzothiophenyl, and benzothiazolyl. The above groups are unsubstituted or substituted as explicitly defined. Particular examples are 1 H-indol-2-yl, 1 H-indol-3-yl, 1 H-indol-4-yl, 1 H-indol-5-yl, 1 H-indol-6-yl, 1 -methyl-1 H-indol-5-yl, 1 H-indazol-5-yl, 1 H-indazol-6-yl, 1 -methyl-1 H- indazol-6-yl, 3-methyl-1 H-indazol-6-yl, 3-methoxy-1 H-indazol-6-yl, 6-methoxy-1 H-indazol-5-yl, 1 H-benzoimidazol- 5-yl, 2-methyl-1 H-benzoimidazol-5-yl, 2-trifluoromethyl-1 H-benzoimidazol-5-yl, 1 H-benzotriazol-5-yl, 2-methyl- benzooxazol-5-yl, 2-methyl-benzooxazol-6-yl, quinoxalin-6-yl, isoquinolin-7-yl, quinolin-6-yl, 1 H-pyrrolo[2,3- c]pyridin-3-yl, 1 H-pyrrolo[2,3-b]pyridin-3-yl, 1 H-pyrrolo[2,3-b]pyridin-5-yl, 1 -methyl-1 H-pyrrolo[2,3-b]pyridin-5-yl, imidazo[1 ,2-a]pyridin-6-yl, 2-carboxy-1 H-indol-5-yl, 3-carboxy-1 H-indol-6-yl, 4-carboxy-1 H-indol-2-yl, 5-carboxy- 1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol-4-yl, 7-carboxy-1 -methyl-1 H- indol-4-yl, 5-(methoxycarbonyl)-1 H-indol-2-yl, 6-(methoxycarbonyl)-1 H-indol-2-yl), 6-carboxy-benzofuran-2-yl, 3- carboxy-benzofuran-6-yl, 2-carboxy-benzofuran-5-yl, and 2-carboxy-benzofuran-6-yl. Preferred examples are 1 H- benzoimidazol-5-yl, 1 H-indol-6-yl, 1 H-indol-5-yl, 1 H-indol-2-yl, 1 H-indazol-5-yl, as well as 8- to 10-membered bicyclic heteroaryl which are mono-substituted with -(C ₀ -3)alkylene-COOR° ² such as 3-carboxy-1 H-indol-6-yl, 4- carboxy-1 H-indol-2-yl, 5-carboxy-1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol-2-yl, 5- (methoxycarbonyl)-l H-indol-2-yl, 6-(methoxycarbonyl)-1 H-indol-2-yl), 6-carboxy-benzofuran-2-yl, 3-carboxy- benzofuran-6-yl, 2-carboxy-benzofuran-5-yl, and 2-carboxy-benzofuran-6-yl. In addition, a further example is 7- carboxy-benzothiophen-2-yl.

For the substituent "-(ChbV-HET, wherein p represents the integer 0 or 1 , and wherein HET represents a 5- or 6- membered heteroaryl", such 5- or 6-membered heteroaryl is as defined before; notably a nitrogen containing 5- membered heteroaryl such as especially tetrazolyl, or oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, or triazolyl. The above groups are unsubstituted or substituted as explicitly defined. The group -(CH ₂ ) _P - is preferably absent, i.e. p represents the integer 0 and the group HET is directly bound to Ar ¹ . Particular examples of -(CH2) _P -HET are especially the -(ChbyHET groups 1 H-tetrazol-5-yl, 3-hydroxy- isoxazol-5-yl, 2-hydroxy-[1 ,3,4]oxadiazol-4-yl; further examples are 3-amino-isoxazol-5-yl, 2-amino-oxazol-5-yl, 5- amino-[1 ,3,4]thiadiazol-2-yl, 5-methylamino-[1 ,3,4]thiadiazol-2-yl, 5-methoxy-[1 ,2,4]oxadiazol-3-yl, 5-amino- [1 ,2,4]oxadiazol-3-yl, 5-[(2-hydroxy-ethyl)]-amino)-[1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5- (oxetan-3-yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, and 2,5-dimethyl-1 H-imidazol-4-yl; as well as 1 H-pyrazol-1 -yl, 1 H-pyrazol-3-yl, 3-methyl-pyrazol-1-yl, 1-methyl-1 H-pyrazol-3-yl, 5-methyl-1 H-pyrazol- 3-yl, 3,5-dimethyl-pyrazol-1-yl, 4-carboxy-1 H-pyrazol-3-yl, 1 H-imidazol-2-yl, 3-methyl-3H-imidazol-4-yl, 2-methyl- 1 H-imidazol-4-yl, 1 ,5-dimethyl-1 H-imidazol-2-yl, 1 ,2-dimethyl-1 H-imidazol-4-yl, 1 ,5-dimethyl-1 H-imidazol-4-yl, 2- cyclopropyl-1 H-imidazol-4-yl, 2-cyclopropyl-1 -methyl-1 H-imidazol-4-yl, [1 ,2,4]oxadiazol-5-yl, 5-methyl- [1 ,2,4]oxadiazol-3-yl, 3-methyl-[1 ,2,4]oxadiazol-5-yl, 5-methyl-[1 ,3,4]oxadiazol-2-yl, isothiazol-5-yl, thiazol-2-yl, thiazol-4-yl, 4-methyl-thiazol-2-yl, 2-methyl-thiazol-4-yl, 2-amino-5-methyl-thiazol-4-yl, 4,5-dimethyl-thiazol-2-yl, 4- carboxy-thiazol-2-yl, 2-carboxy-thiazol-4-yl, 2-hydroxy-thiazol-4-yl, 2-amino-2-oxoethyl)thiazol-4-yl, isoxazol-3-yl, isoxazol-5-yl, 3-methyl-isoxazol-5-yl, 4-methyl-isoxazol-5-yl, 4-carboxy-3-methyl-isoxazol-5-yl, oxazol-5-yl, 2- methyl-oxazol-5-yl, 2-(2-carboxyethyl)-oxazol-5-yl, 2-(2-carboxyethyl)-4-methyl-oxazol-5-yl, 4H-[1 ,2,4]triazol-3-yl, 1 H-[1 ,2,4]triazol-1-yl, 2-methyl-2H-[1 ,2,4]triazol-3-yl, pyridin-2-yl, 4-fluoro-pyridin-2-yl, pyrimidin-2-yl, 5-fluoro- pyrimidin-2-yl, 5-methoxy-pyrimidin-2-yl, 4-methoxy-pyrimidin-2-yl, 6-methoxy-pyrimidin-4-yl, 6-dimethylamino- pyrimidin-4-yl, pyrazin-2-yl, 6-methoxy-pyrazin-2-yl, 6-methoxy-pyridazin-3-yl, 3H-imidazol-4-yl, 3H-[1 ,2,3]triazol-4- yl, oxazol-2-yl, and 4,5-dimethyl-oxazol-2-yl. For avoidance of doubt, certain groups having tautomeric forms which may be considered predominantly aromatic (such as for example 3-hyd roxy-isoxazolyl or 2-hydroxy- [1 ,3,4]oxadiazolyl groups) are defined herein as heteroaryl groups HET, even though their corresponding tautomeric form (3-oxo-2,3-dihydro-2H-isoxazolyl, respectively, 2-oxo-2,3-dihydro-3H-[1 ,3,4]oxadiazolyl) could also be considered as a non-aromatic group. Likewise, certain groups having tautomeric forms which may be considered predominantly non-aromatic (such as 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl or 5-thioxo-4,5-dihydro- [1 ,2,4]oxadiazol-3-yl) as defined for the substituent HET ¹ , are defined herein as not being part of substituted heteroaryl groups as defined for HET, even though their corresponding tautomeric form (5-hydroxy- [1 ,2,4]oxadiazolyl, respectively, 5-mercapto-[1 ,2,4]oxadiazolyl), could also be considered as an heteroaryl group. It is understood that the corresponding tautomer is encompassed in the respective scope as defined.

The term "cyano" refers to a group -CN.

The term "oxo" refers to a group =0 which is preferably attached to a chain or ring carbon or sulfur atom as for example in a carbonyl group -(CO)-, or a sulfonyl group -(SO2)-.

Examples of "-X ² -NR ^N1 R ^N2 " groups as used for substituents of Ar ¹ being phenyl or 5- or 6-membered heteroaryl are amino, methylamino, ethylamino, propylamino, amino-methyl, methylamino-methyl, isobutylamino-methyl, cyclopropylamino-methyl, cyclobutylamino-methyl, (2-methoxyethyl)amino-methyl, (2,2,2-trifluoro-ethyl)-amino; or -NH-CO-H, -N(C ₂ H ₅ )-CO-H, -NH-CO-C2H5, -NH-CO-CH2-CH2-OH, -NH-CO-O-CH3, -N(CH ₃ )-CO-0-CH ₃ ; or pyrrolidin-1-yl, 2-oxo-pyrrolidin-1-yl, 1 ,1-dioxo-isothiazolidin-2-yl, morpholin-4-yl, azetidin-1 -yl, or piperidin-1 -yl; and 2-(dimethylamino)-ethoxy.

Examples of a group "-NH-CO-NR ^N5 R ^N6 " as used for substituents of the group Ar ¹ are ureido (-NH-CO-NH2) and 3-ethylureido (-NH-CO-NH-C2H5).

Examples of a group "-(CH2) _r -CO-NR ^N3 R ^N4 wherein r represents the integer 0 or 1 " as used for substituents of the group Ar ¹ are preferably groups wherein r represents the integer 0 and at least one of R ³ and R ⁴ represents hydrogen (or less preferred, methyl). Particular examples of such group -CO-NR ^N3 R ^N4 are -CO-NH2, -CO-NH(CH3), -CO-N(CH ₃ ) ₂ , -CO-NH(C ₂ H ₅ ), -CO-NH-O-methyl, -CO-NH-O-ethyl, -CO-NH-O-isopropyl, -CO-NH-C2H4-OH, - CO-NH-O-C2H4-OH, -CO-NH-C2H4-OCH3, -CO-NH-C ₂ H ₄ -N(CH ₃ )2, and -CO-NH-O-benzyl. Further examples are- CO-NH-isopropyl and -CO-NH-OH, as well as -CO-N(CH ₃ ) ₂ .

Examples of a group "-X ¹ -CO-R ⁰¹ " as used for substituents of the group Ar ¹ are especially the following groups: a) X ¹ represents a direct bond; and R ⁰¹ represents -OH; (i.e. -X ¹ -CO-R ⁰¹ represents -COOH); or b) X ¹ represents a direct bond; and R ⁰¹ represents (especially ethoxy, or methoxy); (i.e. -X ¹ - CO-R ⁰¹ represents -CO-(Ci-4)alkoxy (especially ethoxycarbonyl, methoxycarbonyl)); or

c) X ¹ represents a direct bond; and R ⁰¹ represents -NH-S02-R ^S3 ; wherein R ^S3 represents (C3- 6)cycloalkyl wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (C3-6)cycloalkyl-(Ci- 3)alkylene wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (Ci-3)fluoroalkyl; phenyl; or -NH2; (i.e. -X ¹ -CO-R ⁰¹ represents -CO-NH-S02-R ^S3 wherein R ^S3 represents the above mentioned groups; notably methyl, ethyl, isopropyl, cyclopropyl, trifluoromethyl, amino; especially -X ¹ -CO-R ⁰¹ represents -

CO-NH-SO2-CH3, -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH-S0 ₂ -cyclopropyl, -CO-NH-S0 ₂ -ethyl, or -CO-NH-SO2- NH ₂ ); or

d) X ¹ represents (Ci. ₃ )alkylene (especially -CH ₂ -, -CH2-CH2-), -0-(Ci- ₃ )alkylene-* (especially -O-CH2-*, -0- CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, O-CH2-CH2-*), -NH-(Ci- ₃ )alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -S- CH2-*, -CF2-, -CH=CH-, or -CH≡CH- [in a sub-embodiment X ¹ represents especially -O-CH2-*, -NH-CH ₂ - *, -S-CH2-*, or (Ci-3)alkylene]; wherein the asterisks indicate the bond that is linked to the -CO-R ⁰¹ group; and R ⁰¹ represents -OH (i.e. -X ¹ -CO-R ⁰¹ represents -X ¹ -COOH wherein X ¹ represents the above mentioned groups; especially -X ¹ -CO-R ⁰¹ represents -O-CH2-COOH or -NH-CH2-COOH; as well as -CH ₂ - COOH, -CH2-CH2-COOH, -CH=CH-COOH, -CH≡CH-COOH, -O-CH2-CH2-COOH, -0-CH(CH ₃ )-COOH, or

-NH-CH(CH ₃ )-COOH); or

e) -X ¹ represents -NH-CO-* or -CO-; wherein the asterisk indicates the bond that is linked to the -CO-R ⁰¹ group; and R ⁰¹ represents -OH (i.e. -X ¹ -CO-R ⁰¹ represents -X ¹ -COOH wherein X ¹ represents the above mentioned groups; especially -X ¹ -CO-R ⁰¹ represents -NH-CO-COOH, -CO-COOH); or

f) X ¹ represents (C^cycloalkylene; and R ⁰¹ represents -OH; (i.e. -X ¹ -CO-R ⁰¹ represents (C3-6)cycloalkyl which is mono-substituted with COOH; especially -X ¹ -CO-R ⁰¹ represents 1 -carboxy-cyclopropan-1-yl or 1-carboxy-cyclopentan-1 -yl); or

g) X ¹ represents a direct bond; and R ⁰¹ represents -O-CH2-CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci- 4)alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ; especially -X ¹ -CO-R ⁰¹ represents -CO-O-CH2-COOH; or

wherein each of the groups a), b), c), d), e), f), and g) forms a particular sub-embodiment.

Compounds of Formula (I) / formula (II) containing a group "-X ¹ -CO-R ⁰¹ " wherein X ¹ represents -CH=CH- may be in E- or Z-configuration. Preferably, such groups are in E-configuration.

Whenever a group Ar ¹ is substituted with a substituent comprising a carboxylic acid group -COOH (such as in the substituents -(Co-3)alkylene-COOR ⁰² wherein R ⁰² repesents hydrogen; -(Co-3)alkylene-COOR ⁰³ wherein R ⁰³ repesents hydrogen; or in the substituents -X ¹ -CO-R ⁰¹ wherein R ⁰¹ represents -OH, especially in the -X ¹ -CO-R ⁰¹ groups a), d), e) and f) above) such carboxylic acid group may be present in form of a prodrug group. Such prodrugs are encompassed in the scope of the present invention. In certain instances, compounds comprising such carboxylic acid prodrug groups may as such exhibit biological activity on the EP2 and/or EP4 receptor, whereas in other instances, such compounds comprising such carboxylic acid prodrug groups require (e.g. enzymatic) cleavage of the prodrug to exhibit biological activity on the EP2 and/or EP4 receptor. Prodrugs of the carboxylic acid functional group are well known in the art (see for example J. Rautio (Ed.) Prodrugs and Targeted Delivery: Towards Better ADME Properties, Volume 47, Wiley 2010JSBN: 978-3-527-32603-7; H. Maag in Stella, V., Borchardt, R., Hageman, M., Oliyai, R., Maag, H.Jilley, J. (Eds.) Prodrugs: Challenges and Rewards, Springer 2007, ISBN 978-0-387-49785-3).

Particular examples of prodrugs, for example suitable for -X ¹ -COOH groups are:

• ester groups -X ¹ -CO-0-P ¹ wherein P ¹ is for example (C3-6)cycloalkyl wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (C3-6)cycloalkyl-(Ci_3)alkyl wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (Ci-3)fluoroalkyl; hydroxy-(C2 )alkyl; or (Ci-4)alkoxy-(C2-4)alkyl (especially P ¹ is (Ci )alkyl, in particular methyl or ethyl); • groups -X ¹ -CO-NH-S02-R ^S3 wherein R ^S3 represents (C3-6)cycloalkyl wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (C3-6)cycloalkyl-(Ci_3)alkyl wherein the (C3-6)cycloalkyl optionally contains a ring oxygen atom; (Ci-3)fluoroalkyl, -NH ₂ ; (especially R ^S3 is (Ci- ₄ )alkyl, (C3-6)cycloalkyl; in particular methyl);

· groups -X ¹ -CO-R ⁰¹ wherein R ⁰¹ represents -O-CH2-CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci- 4)alkoxy, or -N[(Ci. ₄ )alkyl] ₂ (especially -CO-O-CH2-COOH, -CO-0-CH ₂ -CO-N(CH ₃ ) ₂ );

• groups -X ¹ -CO-R ⁰¹ wherein R ⁰¹ represents -O-CH2-O-CO-R ⁰⁵ , wherein R ⁰⁵ repesents or (Ci- 4)alkoxy (especially -CO-0-CH ₂ -0-CO-0-ethyl, -CO-0-CH ₂ -0-CO-propyl);

• groups -X -CO-R ⁰¹ wherein R ⁰ represents -O-CH2-CH2-N [(Ci- ₄ )alkyl] ₂ (especially -CO-O-CH2-CH2- N(CH ₃ ) ₂ ); and

• groups -X ¹ -CO-R ⁰¹ wherein R ⁰¹ represents 5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-.

Examples of "hydroxy-(Ci- ₄ )alkyl" groups as used for substituents of the group Ar ¹ are hydroxymethyl and 1 - hydroxy-ethyl.

An example of "dihydroxy-(C2- ₄ )alkyl" groups as used for substituents of the group Ar ¹ is 1 ,2-dihydroxyethyl. An example of "hydroxy-(C2 )alkoxy" groups as used for substituents of the group Ar ¹ is 2-hydroxy-ethoxy.

An example of "(Ci )alkoxy-(C2 )alkoxy" groups as used for substituents of the group Ar ¹ is 2-methoxy-ethoxy.

Examples of a group "-S0 ₂ -R ^S1 " as used for substituents of the group Ar ¹ are -SO2-CH3, -SO2-NH2, -SO2-NH-CH3.

Examples of a group " S-R ^S2 " as used for substituents of the group Ar ¹ are methylsulfanyl, ethylsulfanyl, n- propylsulfanyl, isopropylsulfanyl, isobutylsulfanyl), cyclobutylsulfanyl, and (oxetan-3-yl)-sulfanyl.

An example of a "(Ci- ₄ )alkoxy-(C2- ₄ )alkyl" group is 2-methoxyethyl.

An example of a "hydroxy-(C2- ₄ )alkoxy" group is 2-hydroxy-ethoxy.

An example of a "hydroxy-(C2- ₄ )alkyl" group is 2-hydroxy-ethyl.

An example of a "-CO-(Ci- ₄ )alkoxy" group as used for substituents of the group Ar ¹ is ethoxycarbonyl. Such groups may also be useful as produgs of the respective -COOH substituent.

Whenever the word "between" is used to describe a numerical range, it is to be understood that the end points of the indicated range are explicitly included in the range. For example: if a temperature range is described to be between 40 °C and 80 °C, this means that the end points 40 °C and 80 °C are included in the range; or if a variable is defined as being an integer between 1 and 4, this means that the variable is the integer 1 , 2, 3, or 4.

Unless used regarding temperatures, the term "about" placed before a numerical value "X" refers in the current application to an interval extending from X minus 10% of X to X plus 10% of X, and preferably to an interval extending from X minus 5% of X to X plus 5% of X. In the particular case of temperatures, the term "about" placed before a temperature "Y" refers in the current application to an interval extending from the temperature Y minus 10°C to Y plus 10°C, and preferably to an interval extending from Y minus 5°C to Y plus 5°C. Besides, the term "room temperature" as used herein refers to a temperature of about 25°C.

Further embodiments of the invention are presented hereinafter:

9) Another embodiment relates to compounds according to embodiment 8), wherein Ar ¹ represents

· a phenyl group of the structure (Ar-I):

(Ar-I)

wherein

• R ^p represents

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci- ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH ₂ - CH ₂ -), -0-(Ci- ₃ )alkylene-* (especially -0-CH ₂ -*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci- ₃ )alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -CH=CH-, -CH≡CH-, -NH-CO- *, or (C ₃ -5)cycloalkylene; wherein the asterisks indicate the bond that is linked to the -CO- R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci )alkyl, (C ₃ -6)cycloalkyl wherein the (C ₃ .

6)cycloalkyl optionally contains a ring oxygen atom, (C ₃ -6)cycloalkyl-(Ci- ₃ )alkylene wherein the (C ₃ -6)cycloalkyl optionally contains a ring oxygen atom, (Ci- 3)fluoroalkyl, or -NH ₂ ;

^■ -0-CH ₂ -CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci )alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ;

^■ -0-CH ₂ -0-CO-R ⁰⁵ , wherein R ⁰⁵ repesents (Ci- ₄ )alkyl or (Ci )alkoxy;

■ -0-CH ₂ -CH ₂ -N[(Ci )alkyl] ₂ (especially -0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ ); or

^■ (5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-0-CH ₃ , -CO-0-C ₂ H ₅ , -0- CH ₂ -COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ -COOH, - NH-CH ₂ -CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH- S0 ₂ -cyclopropyl, -CO-NH-S0 ₂ -C ₂ H ₅ , -CO-NH-S0 ₂ -NH ₂ , -CO-0-CH ₂ -COOH, -CO-0-CH ₂ -CH ₂ -

N(CH ₃ ) ₂ , -CO-0-CH ₂ -CO-N(CH ₃ ) ₂ , -CO-0-CH ₂ -0-CO-0-C ₂ H ₅ , -CO-0-CH ₂ -0-CO-propyl, (5- methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyl-0-CO-, -CH ₂ -COOH, -CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , - CH2-CH2-COOH, -CH=CH-C00H, -CH≡CH-CO-0-C ₂ H ₅ , -NH-C0-C00H, 1-carboxy- cyclopropan-1 -yl];

N ^0H

A

' NH ₂ .

> -NH-CO-NR ^N5 R ^N6 wherein R ^N5 and R ⁶ independently represent hydrogen or (wherein preferably at least one of R ⁵ and R ⁶ represents hydrogen; and wherein particular examples of such group -NH-CO-NR ⁵ R ⁶ are -NH-CO-NH2, -NH-CO-NH-C2H5);

-(CH2)q-HET ¹ , wherein q represents the integer 0, 1 or 2 (especially q is 0, i.e. HET ¹ is linked to Ar ¹ by a direct bond); and wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hyd roxy-[1 ,2,4]oxadiazol-3-yl ) , or 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2,4]oxadiazol-5-yl);

-(CH2)p-HET, wherein p represents the integer 0 or 1 (especially p is 0, i.e. HET is linked to Ar ¹ by a direct bond); and wherein HET represents a 5-membered heteroaryl (especially oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl), wherein said 5-membered heteroaryl is unsubstituted, or mono- or di-substituted, wherein the substituents are independently selected from (especially methyl), (Ci-4)alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3-s)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or -NR ^N9 R ^N10 wherein R ^N9 and R ^N1 ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or hydroxy-(C2 )alkyl (especially 2-hydroxy-ethyl); (especially such group -(CH ₂ ) _P -HET is 1 H-tetrazol-5-yl, 3-hyd roxy-i soxazol -5-y 1 , 2-hydroxy- [1 ,3,4]oxadiazol-4-yl, 3-amino-isoxazol-5-yl, 2-amino-oxazol-5-yl, 5-amino-[1 ,3,4]thiadiazol-2-yl, 5- methylamino-[1 ,3 ,4]th iad iazol-2-yl , 5-methoxy-[1 ,2 ,4]oxad iazol-3-y 1 , 5-amino-[1 ,2,4]oxadiazol-3-yl, 5- [(2-hydroxy-ethyl)]-amino)-[1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5-(oxetan-3- yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, 2,5-dimethyl-1 H-imidazol-4-yl); R ^m1 represents

> hydrogen;

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl);

> (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> (C3-6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy;

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy); > -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); wherein in a sub-embodiment, R ^m1 especially is different from hydrogen;

• R ^m2 represents hydrogen, methyl, fluoro, or chloro; and

• R ⁰¹ represents hydrogen; or, in case R ^m2 represents hydrogen, R ⁰¹ represents hydrogen or fluoro;

or Ar ¹ represents a 5-membered heteroaryl group of the structure (Ar-ll):

(Ar-ll)

wherein

• Y represents CR ⁸ wherein R ⁸ represents especially hydrogen, or halogen (notably fluoro, chloro); or Y represents N;

• R ⁷ represents

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci- ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH2-CH2-), -0-(Ci. ₃ )alkylene- ^* (especially -O-CH2-*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci- 3)alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -CH=CH-, -CH≡CH-, -NH-CO-*, or (C ₃ . 5)cycloalkylene; wherein the asterisks indicate the bond that is linked to the -CO-R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci-4)alkyl, (C ₃ -6)cycloalkyl wherein the (C ₃ .

6)cycloalkyl optionally contains a ring oxygen atom, (C ₃ -6)cycloalkyl-(Ci- ₃ )alkylene wherein the (C ₃ -6)cycloalkyl optionally contains a ring oxygen atom, (Ci- ₃ )fluoroalkyl, or -NH ₂ ;

^■ -0-CH ₂ -CO-R ⁰⁴ , wherein R ⁰⁴ repesents hydroxy, or (Ci- ₄ )alkoxy, or -N[(Ci- ₄ )alkyl] ₂ ;

■ -0-CH ₂ -0-CO-R ⁰⁵ , wherein R ⁰⁵ repesents or (Ci- ₄ )alkoxy; or

■ -0-CH ₂ -CH ₂ -N[(Ci- ₄ )alkyl] ₂ (especially -0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ );

^■ (5-methyl-2-oxo-[1 ,3]dioxol-4-yl)-methyloxy-;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-0-CH ₃ , -CO-0-C ₂ H ₅ , -O-CH2- COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ -COOH, -NH-CH ₂ - CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH-S0 ₂ - cyclopropyl, -CO-NH-SO2-C2H5, -CO-NH-SO2-NH2, -C0-0-CH ₂ -C00H, -CO-0-CH ₂ -CH ₂ -N(CH ₃ ) ₂ , - CO-0-CH ₂ -CO-N(CH ₃ ) ₂ , -CO-0-CH ₂ -0-CO-0-C ₂ H ₅ , -CO-0-CH ₂ -0-CO-propyl, (5-methyl-2-oxo- [1 ,3]dioxol-4-yl)-methyl-0-CO-, -CH ₂ -C00H, -CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , -CH ₂ -CH ₂ -COOH, - CH=CH-C00H, -CH≡CH-CO-0-C ₂ H ₅ , -NH-C0-C00H, 1 -carboxy-cyclopropan-1 -yl];

> -NH-CO-NR ^N5 R ^N6 wherein R ^N5 and R ^N6 independently represent hydrogen or (Ci-4)alkyl (wherein preferably at least one of R ⁵ and R ⁶ represents hydrogen; and wherein particular examples of such group -NH-CO-NR ⁵ R ⁶ are -NH-CO-NH ₂ , -NH-CO-NH-C ₂ H ₅ );

-(CH ₂ )q-HET ¹ , wherein q represents the integer 0, 1 or 2 (especially q is 0, i.e. HET ¹ is linked to Ar ¹ by a direct bond); and wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hyd roxy-[1 ,2,4]oxadiazol-3-yl ) , or 3-oxo-2,3-dihydro- [1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2,4]oxadiazol-5-yl);

-(CH ₂ ) _P -HET, wherein p represents the integer 0 or 1 (especially p is 0, i.e. HET is linked to Ar ¹ by a direct bond); and wherein HET represents a 5-membered heteroaryl (especially oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl), wherein said 5-membered heteroaryl is unsubstituted, or mono- or di-substituted, wherein the substituents are independently selected from (especially methyl), (Ci )alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3-5)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or -NR ^N9 R ^N10 wherein R ^N9 and R ^N1 ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or hydroxy-(C ₂ )alkyl (especially 2-hydroxy-ethyl); (especially such group -(CH ₂ ) _P -HET is 1 H-tetrazol-5-yl , 3-hydroxy-isoxazol-5-yl, 2-hydroxy- [1 ,3,4]oxadiazol-4-yl, 3-amino-isoxazol-5-yl, 2-amino-oxazol-5-yl, 5-amino-[1 ,3,4]thiadiazol-2-yl, 5- methylamino-[1 ,3,4]thiadiazol-2-yl, 5-methoxy-[1 ,2,4]oxadiazol-3-yl, 5-amino-[1 ,2,4]oxadiazol-3-yl, 5- [(2-hydroxy-ethyl)]-amino)-[1 ,2,4]oxadiazol-3-yl, 5-hydroxymethyl-[1 ,2,4]oxadiazol-3-yl, 5-(oxetan-3- yl)-[1 ,2,4]oxadiazol-3-yl, 1 H-imidazol-4-yl, 5-methyl-1 H-imidazol-4-yl, 2,5-dimethyl-1 H-imidazol-4-yl); R ⁶ represents

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl);

> (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> (C3-6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy-(C ₂ )alkoxy (especially 2-hydroxy-ethoxy);

> -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); • or Ar ¹ represents 8- to 10-membered bicyclic heteroaryl (notably 9- or 10-membered bicyclic heteroaryl; especially indazolyl, benzoimidazolyl, indolyl, benzofuranyl, benzooxazolyl, quinoxalinyl, isoquinolinyl, or quinolinyl); wherein said 8- to 10-membered bicyclic heteroaryl independently is mono-substituted with -(Co- )alkylene-COOR ⁰² wherein R ⁰² repesents hydrogen or (Ci )alkyl (especially methyl) (wherein especially such group -(Co )alkylene-COOR ⁰² is -COOH); (especially such 8- to 10-membered bicyclic heteroaryl is 3-carboxy- 1 H-indol-6-yl, 4-carboxy-1 H-indol-2-yl, 5-carboxy-1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol- 2-yl, 5-(methoxycarbonyl)-1 H-indol-2-yl, 6-(methoxycarbonyl)-1 H-indol-2-yl), 6-carboxy-benzofuran-2-yl, 3- carboxy-benzofuran-6-yl, 2-carboxy-benzofuran-5-yl, or 2-carboxy-benzofuran-6-yl); wherein in a sub-embodiment, Ar ¹ especially is a phenyl group of the structure (Ar-I) (wherein in particular R ^m1 especially is different from hydrogen), or a 5-membered heteroaryl group of the structure (Ar-ll), as defined herein above.

10) Another embodiment relates to compounds according to any one of embodiment 8) to 15), wherein Ar ¹ represents

• a phenyl group of the structure (Ar-I):

(Ar-I)

wherein

• R ^p represents

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci- ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH ₂ -

CH ₂ -), -0-(Ci- ₃ )alkylene-* (especially -0-CH ₂ -*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci- ₃ )alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -CH=CH-, -NH-CO-*, or (C ₃ . )cycloalkylene; wherein the asterisks indicate the bond that is linked to the -CO-R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci )alkyl, (C )cycloalkyl wherein the (C ₃ .

)cycloalkyl optionally contains a ring oxygen atom, (C )cycloalkyl-(Ci- ₃ )alkylene wherein the (C )cycloalkyl optionally contains a ring oxygen atom, (Ci-

₃ )fluoroalkyl, or -NH ₂ ; [wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-O-CH3, -CO-O-C2H5, -0- CH2-COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH2-COOH, - NH-CH2-CO-O-CH3, -NH-CH(CH ₃ )-COOH, -CO-NH-SO2-CH3, -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH- S0 ₂ -cyclopropyl, -CO-NH-SO2-C2H5, -CO-NH-SO2-NH2, -CH2-COOH, -CH2-CO-O-CH3, -CH∑- CO-O-C2H5, -CH2-CH2-COOH, -CH=CH-COOH, -NH-CO-COOH, 1 -carboxy-cyclopropan-1 -yl];

> HET ¹ , wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl), or 3-oxo-2,3-dihydro-[1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2 ,4]oxad iazol-5-yl ) ;

> HET, wherein HET represents a 5-membered heteroaryl selected from oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl; in particular isoxazolyl and tetrazolyl, wherein said 5-membered heteroaryl is unsubstituted, or mono-substituted, wherein the substituent is independently selected from (Ci-4)alkyl (especially methyl), (Ci )alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci-3)alkyl (especially hydroxymethyl), (C3- 5)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or - N RN9RM0 wherein R ^N9 and R ¹ ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or h yd roxy-(C2-4)al ky I (especially 2-hydroxy-ethyl); [in particular HET is unsubstituted or mono- substituted with hydroxy; especially HET is 1 H-tetrazol-5-yl, 3-hydroxy-isoxazol-5-yl, or 2-hydroxy- [1 ,3,4]oxadiazol-4-yl];

• R ^m1 represents

> hydrogen;

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl);

> (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> (C3-6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy;

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy);

> -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl); wherein in a sub-embodiment, R ^m1 especially is different from hydrogen;

• R ^m2 represents hydrogen, methyl, fluoro, or chloro; and

• R ⁰¹ represents hydrogen; or Ar ¹ represents a 5-membered heteroaryl group of the structure (Ar-ll):

(Ar-ll)

wherein

• Y represents CH or N;

• R ⁷ represents

> -X -CO-R ⁰¹ , wherein

> X ¹ represents a direct bond, (Ci- ₃ )alkylene (especially -CH ₂ -, -CH(CH ₃ )-, -C(CH ₃ ) ₂ -, -CH2-CH2-), -0-(Ci. ₃ )alkylene-* (especially -O-CH2-*, -0-CH(CH ₃ )-*, -0-C(CH ₃ ) ₂ -*, -0-CH ₂ -CH ₂ -*), -NH-(Ci- 3)alkylene-* (especially -NH-CH ₂ -*, -NH-CH(CH ₃ )-*), -S-CH ₂ -*, -CF ₂ - -CH=CH-, -CH≡CH-, -NH- CO-*, -CO-, or (C ₃ -5)cycloalkylene; wherein the asterisks indicate the bond that is linked to the - CO-R ⁰¹ group; and

> R ⁰¹ represents

^■ -OH;

^■ -0-(Ci )alkyl (especially ethoxy, methoxy);

^■ -NH-S0 ₂ -R ^S3 wherein R ^S3 represents (Ci-4)alkyl, (C ₃ -6)cycloalkyl wherein the (C ₃ .

6)cycloalkyl optionally contains a ring oxygen atom, (C ₃ -6)cycloalkyl-(Ci- ₃ )alkylene wherein the (C ₃ -6)cycloalkyl optionally contains a ring oxygen atom, (Ci- ₃ )fluoroalkyl, or -NH ₂ ;

[wherein in particular such group -X -CO-R ⁰¹ represents -COOH, -CO-0-CH ₃ , -CO-0-C ₂ H ₅ , -O-CH2- COOH, -0-CH(CH ₃ )-COOH, -0-C(CH ₃ ) ₂ -COOH, -0-CH ₂ -CH ₂ -COOH, -NH-CH ₂ -COOH, -NH-CH ₂ - CO-0-CH ₃ , -NH-CH(CH ₃ )-COOH, -CO-NH-S0 ₂ -CH ₃ , -CO-NH-S0 ₂ -C(CH ₃ ) ₂ , -CO-NH-S0 ₂ - cyclopropyl, -CO-NH-S0 ₂ -C ₂ H ₅ , -CO-NH-S0 ₂ -NH ₂ , -CH ₂ -COOH, -CH ₂ -CO-0-CH ₃ , -CH ₂ -CO-0-C ₂ H ₅ , -CH ₂ -CH ₂ -COOH, -CH=CH-COOH, -NH-CO-COOH, 1 -carboxy-cyclopropan-1 -yl];

> HET ¹ , wherein HET ¹ represents 5-oxo-4,5-dihydro-[1 ,2,4]oxadiazol-3-yl (encompassing its tautomeric form 5-hydroxy-[1 ,2,4]oxadiazol-3-yl), or 3-oxo-2,3-dihydro-[1 ,2,4]oxadiazol-5-yl (encompassing its tautomeric form 3-hydroxy-[1 ,2 ,4]oxad iazol-5-yl ) ;

> HET, wherein HET represents a 5-membered heteroaryl selected from oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, imidazolyl, pyrazolyl, triazolyl, or tetrazolyl; in particular isoxazolyl and tetrazolyl, wherein said 5-membered heteroaryl is unsubstituted, or mono-substituted, wherein the substituent is independently selected from (Ci-4)alkyl (especially methyl), (Ci )alkoxy (especially methoxy), -COOH, hydroxy, hydroxy-(Ci- ₃ )alkyl (especially hydroxymethyl), (C ₃ . 5)cycloalkyl optionally containing one ring oxygen atom (especially cyclopropyl, oxetan-3-yl), or - N RN9RM0 wherein R ^N9 and R ¹ ° independently represent hydrogen, (Ci-3)alkyl (especially methyl), or hydroxy-(C2 )alkyl (especially 2-hydroxy-ethyl) [in particular HET is unsubstituted or mono- substituted with hydroxy; especially HET is 1 H-tetrazol-5-yl, 3-hyd roxy-i soxazol -5-y I , or 2-hydroxy- [1 ,3,4]oxadiazol-4-yl];

• R ⁶ represents

> (Ci-e)alkyl (especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl);

> (Ci-4)alkoxy (especially methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy);

> (Ci-3)fluoroalkyl (especially trifluoromethyl);

> (Ci-3)fluoroalkoxy (especially difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy);

> halogen (especially fluoro or chloro);

> hydroxy;

> (C ₃ -6)cycloalkyl (especially cyclopropyl);

> (C3-6)cycloalkyl-oxy (especially cyclopropyl-oxy, cyclobutyl-oxy, cyclopentyl-oxy);

> hydroxy-(C2 )alkoxy (especially 2-hydroxy-ethoxy);

> -S-R ^S2 wherein R ^S2 represents (especially methyl, ethyl, n-propyl, isopropyl, isobutyl), or (C3-6)cycloalkyl optionally containing one ring oxygen atom (especially cyclobutyl, oxetan-3-yl);

• or Ar ¹ represents 8- to 10-membered bicyclic heteroaryl selected from indazolyl, benzoimidazolyl, indolyl, benzofuranyl, benzooxazolyl, quinoxalinyl, isoquinolinyl, and quinolinyl; wherein said 8- to 10-membered bicyclic heteroaryl independently is mono-substituted with -(C ₀ -3)alkylene-COOR° ² wherein R ⁰² repesents hydrogen or (especially methyl) (wherein especially such group -(Co-3)alkylene-COOR ⁰² is -COOH); (especially such 8- to 10-membered bicyclic heteroaryl is 3-carboxy-1 H-indol-6-yl, 4-carboxy-1 H-indol-2-yl, 5- carboxy-1 H-indol-2-yl, 6-carboxy-1 H-indol-2-yl, 7-carboxy-1 H-indol-2-yl, 5-(methoxycarbonyl)-1 H-indol-2-yl, 6- (methoxycarbonyl)-l H-indol-2-yl), 6-carboxy-benzofuran-2-yl, 3-carboxy-benzofuran-6-yl, 2-carboxy- benzofuran-5-yl, or 2-carboxy-benzofuran-6-yl);

wherein in a sub-embodiment, Ar ¹ especially is a phenyl group of the structure (Ar-I) (wherein in particular R ^m1 especially is different from hydrogen), or a 5-membered heteroaryl group of the structure (Ar-ll), as defined herein above.

wherein each of the groups A) and B) forms a particular sub-embodiment;

wherein in a further sub-embodiment, Ar ¹ especially is a phenyl group (in particular a di-substituted phenyl group), or a thiophenyl group, or a thiazolyl group, as defined in groups A) and/or B) herein above.

12) Another embodiment relates to compounds according to embodiment 8), wherein

a) Ar ¹ represents a phenyl group selected from:

• ¹ represents 9- or 10-membered bicyclic heteroaryl selected from

• ¹ represents a group selected from:

wherein in a sub-embodiment, Ar ¹ especially is a phenyl group (in particular a di-substituted phenyl group), or a thiophenyl group, or a thiazolyl group, as defined herein above.

13) Another embodiment relates to compounds according to embodiment 8), wherein

(i) Ar ¹ represents a phenyl group selected from:

a)

wherein in a sub-embodiment, Ar ¹ especially is a phenyl group (in particular a di-substituted phenyl group), or a thiophenyl group, or a thiazolyl group, as defined herein above.

14) Another embodiment relates to compounds according to embodiment 8), wherein Ar ¹ represents a group selected from

A)

or, in addition, Ar ¹ represents a group selected from

wherein each of the groups A) and B) forms a particular sub-embodiment.

15) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 13), wherein X represents S.

16) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 13), wherein X represents 0.

17) A second embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 15), wherein R ² represents hydrogen.

18) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 16), wherein R ² represents (Ci_4)alkyl (especially methyl, ethyl), halogen (especially chloro, bromo), or cyano.

19) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 16), wherein R ² represents (Ci-4)alkyl (especially methyl, ethyl). 20) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 15), wherein R ² represents (Ci-4)alkyl (especially methyl, ethyl), or cyano.

21) Another embodiment relates to compounds of formual (II) according to any one of embodiments 8) to 15), wherein R ² represents cyano.

22) Another embodiment relates to compounds according to any one of embodiments 8) to 21), wherein in the fragment

(R ¹ ) _n represents one, two or three substituents (i.e. said fragment is, in addtition to R ² , substituted with one, two or three R ¹ ), wherein said substituents R ¹ are independently selected from (Ci-3)alkyl (especially methyl), (Ci-3)alkoxy (especially methoxy), halogen (especially fluoro, or chloro), (Ci-3)fluoroalkyl (especially trifluoromethyl), (Ci-3)fluoroalkoxy (especially trifluoromethoxy), or cyano.

23) Another embodiment relates to compounds according to any one of embodiments 8) to 21), wherein in the fragment

(R ¹ ) _n represents one, two or three substituents (i.e. said fragment is, in addtition to R ² , substituted with one, two or three R ¹ ), wherein said substituents R ¹ are independently selected from (Ci-3)alkyl (especially methyl), (Ci-3)alkoxy (especially methoxy), or halogen (especially fluoro, or chloro). 24) Another embodiment relates to compounds according to any one of embodiments 8) to 16), wherein the fragment

represents

·

or, in addition, said fragment may represent the benzothiophene: or a benzofurane selected from:

25) Another embodiment relates to compounds according to any one of embodiments 8) to 16), wherein the

represents a benzothiophene selected from

(especially

26) The invention, thus, relates to compounds of the formula (I) as defined in embodiment 1) for use according to embodiment 1 ), or to such compounds further limited by the characteristics of any one of embodiments 2) to 25), under consideration of their respective dependencies; to pharmaceutically acceptable salts thereof; and to the use of such compounds according to embodiment 1), and as further described herein below. For avoidance of any doubt, especially the following embodiments relating to the compounds of formula (I) are thus possible and intended and herewith specifically disclosed in individualized form:

1, 9+1, 13+1, 14+1, 15+1, 15+9+1, 15+13+1, 15+14+1, 20+15+1, 20+15+9+1, 20+15+13+1, 20+15+14+1, 24+1, 24+9+1, 24+13+1, 24+15+1, 24+15+9+1, 24+15+13+1, 24+15+14+1, 24+20+15+1, 24+20+15+9+1, 24+20+15+13+1, 24+20+15+14+1, 25+1, 25+9+1, 25+14+1, 25+15+1, 25+15+9+1, 25+15+13+1, 25+15+14+1, 25+20+15+1, 25+20+15+9+1, 25+20+15+13+1, 25+20+15+14+1.

In the list above the numbers refer to the embodiments according to their numbering provided hereinabove whereas "+" indicates the dependency from another embodiment. The different individualized embodiments are separated by commas. In other words, "25+15+14+1" for example refers to embodiment 25) depending on embodiment 15), depending on embodiment 14), depending on embodiment 1), i.e. embodiment "25+15+14+8" corresponds to the compounds of formula (I) as defined in embodiment 1 ) for use according to embodiment 1 ), further limited by all the structural features of the embodiments 14), 15), and 25).

27) The invention, thus, further relates to compounds of the formula (II) as defined in embodiment 8), or to such compounds further limited by the characteristics of any one of embodiments 9) to 25), under consideration of their respective dependencies; to pharmaceutically acceptable salts thereof; and to the use of such compounds as medicaments especially in the prevention / prophylaxis or treatment of diseases which respond to the blockage of the EP2 receptors and/or the EP4 receptors as described herein below. For avoidance of any doubt, especially the following embodiments relating to the compounds of formula (II) are thus possible and intended and herewith specifically disclosed in individualized form:

8, 9+8, 10+8, 12+8, 13+8, 14+8, 15+8, 15+9+8, 15+10+8, 15+12+8, 15+13+8, 15+14+8, 18+15+8, 18+15+9+8, 18+15+10+8, 18+15+12+8, 18+15+13+8, 18+15+14+8, 20+15+8, 20+15+9+8, 20+15+10+8, 20+15+12+8, 20+15+13+8, 20+15+14+8, 22+8, 22+10+8, 22+15+8, 22+15+9+8, 22+15+10+8, 22+15+12+8, 22+15+13+8, 22+15+14+8, 22+18+15+8, 22+18+15+9+8, 22+18+15+10+8, 22+18+15+12+8, 22+18+15+13+8, 22+18+15+14+8, 24+8, 24+13+8, 24+15+8, 24+15+9+8, 24+15+10+8, 24+15+12+8, 24+15+13+8, 24+15+14+8, 24+20+15+8, 24+20+15+9+8, 24+20+15+10+8, 24+20+15+12+8, 24+20+15+13+8, 24+20+15+14+8, 25+8, 25+14+8, 25+15+8, 25+15+9+8, 25+15+10+8, 25+15+12+8, 25+15+13+8, 25+15+14+8, 25+20+15+8, 25+20+15+9+8, 25+20+15+10+8, 25+20+15+12+8, 25+20+15+13+8, 25+20+15+14+8.

In the list above the numbers refer to the embodiments according to their numbering provided hereinabove whereas "+" indicates the dependency from another embodiment. The different individualized embodiments are separated by commas. In other words, "25+15+14+8" for example refers to embodiment 25) depending on embodiment 15), depending on embodiment 14), depending on embodiment 8), i.e. embodiment "25+15+14+8" corresponds to the compounds of formula (II) according to embodiment 8) further limited by all the features of the embodiments 14), 15), and 25).

28) Another embodiment relates to compounds of formula (II) according to embodiment 8), which are selected from the following compounds:

5-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-methyl-thiophene-2- carboxylic acid;

4- {6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-ethy lamino]-pyrimidin-4-yl}-2-methylsulfanyl-benzoic acid;

4-{6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin-4-yl}-2-methylsulfanyl-benzoic acid; 3-Ethoxy-5-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pyri

acid;

5- {6 2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-ethylami no]^yrimidin -yl}-3-ethoxy-thiophene-2- carboxylic acid; 5-{6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino ]-pyrimidin-4-yl}-3-ethoxy-th acid;

3-Ethoxy-5-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thioph en-3-yl)-ethylamino]-pyrim

carboxylic acid;

5-{6-[2-(4-Chloro-2J-dimethyl-benzo[b]thioph

acid;

5-{6-[2-(4-ChlorO-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidi

carboxylic acid;

5-{6-[2-(4,5-Difluoro-7-methoxy-2-methyl-benzofuran-3-yl)-et hylamino]-pyrimidin-4-yl}-3-ethoxy-thi carboxylic acid;

3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidi

acid;

5-[6-(2-Benzo[b]thiophen-3-yl-ethylamino)-pyrimidin-4-yl]-3- ethoxy-thiophen acid;

3-Ethoxy-5-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzofuran- 3-yl)-ethylamino]-pyrimidin

carboxylic acid;

5-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin -yl}-3-ethoxy-thi

5-{6-[2-(2 -Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4-yl} -3-e acid;

3- Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzofuran-3-yl)-ethyl amino]-pyrimidin-4-yl}-t^ acid; 5-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-ethoxy-thiophene-2- carboxylic acid;

5-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-(2-h

2-carboxylic acid;

5- {6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin-4-yl}-3-^

carboxylic acid;

4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl) -ethylamino]-pyrimidin acid;

4- {6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin -yl}-2-eth

6- {6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim idin-4-yl}-benzofuran-2-^^ acid;

5- {6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim idin-4-yl}-benzofuran-2-^^ acid;

5-(4-{6-[2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin -yl}-ph

3(2H)-one [tautomeric form: 5-(4-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethy l)amino)pyrimidin-4- yl)phenyl)-[1 ,2,4]oxadiazol-3-ol];

2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-1 H-indole-4-carboxylic acid;

(E)-3-(3-Ethoxy-546-[2-(5-fluoro-2,7-dimethyl-benzo[b]thi ophen-3-yl)-ethylamino]-pyrimidi

acrylic acid;

(4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidi

acid; 2- Difluoromethoxy -{6-[2-(5-fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin

(2-Ethoxy -{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin

acetic acid;

(2-Ethoxy-4-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimi acid; (2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimid

acid;

N-(3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimidin

carbonyl)-methanesulfonamide;

{6-[4-Ethoxy-5-(1 H-tetrazol-5-yl)-thiophen-2-yl]-pyrimidin -yl}-[2-(5-fluoro-2J-dimethyl-benzo

ethyl]-amine;

3- (3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimidin-4-y

[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(3-ethoxy-5-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen- 3- yl)ethyl)amino)pyrimidin-4-yl)thiophen-2-yl)-[1 ,2,4]oxadiazol-5-ol];

4- Ethoxy-2-{6-[2-(5-fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimid

acid; and

3-(4-Ethoxy-2-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrim

[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(4-ethoxy-2-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen- 3- yl)ethyl)amino)pyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol].

29) In addition to the compounds listed in embodiment 28), further compounds of formula (II) according to embodiment 8), are selected from the following compounds:

5- {6 2-(5-Fluoro-2J-dimethyl-benzofuran-3-yl)-ethylamino]^yrimidi n-4-yl}-3-methyl-thiophene-2-carboxylic acid; 5-{6 2-(2J-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin- 4-yl}-3-methyl-thiophene-2-carboxylic acid; 5-{6 2-(5-Chloro-2J-dimethyl-benzofuran-3-yl)-ethylamino]-pyrimid in -yl}-3-methyl-thiophene-2-carboxylic acid;

3- Methyl-5-{6-[2-(2-methyl-benzofuran-3-yl)-ethylamino]-pyrimi din-4-yl}-thiophene-2-carboxylic acid;

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-benzoic acid;

4- {6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin4-yl}-2-hydroxy-benzoic acid; 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin4-yl}-2-hydroxy-benzoic acid;

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin4-yl}-2-methylsulfanyl-benzoic acid;

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidin4-yl}-2-methylsulfanyl- benzoic acid;

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzofuran-3-yl)-ethylamino]- pyrimidin4-yl}-2-methylsulfanyl-benzoic acid; 4-{6 2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-p yrimidin4-yl}-2-methylsulfanyl-benzoic acid; 4-{6-[2-(2-Methyl-benzofuran-3-yl)-ethylamino]-pyrimidin4-yl }-2-methylsulfanyl-benzoic acid;

4-{6-[2-(4-Chloro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-pyrimidin4-yl}-2-methylsulfanyl-benzoic acid; 4-{6 2-(4,7-Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin4-yl}-2-methylsulfanyl-benzoic acid; 4-{6 2-(6-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-p yrimidin4-yl}-2-methylsulfanyl-benzoic acid; 4-{6-[2-(7-Chloro-5-fluoro-2-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin-4-^

acid;

4-{6-[2-(2-Methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimid in-4-yl}-2-methylsulfan acid;

3- Ethoxy-5-{6-[2-(2-ethyl-5-fluoro-7-methyl-benzofuran-3-yl)-e thylamino]-pyrimidin-4-yl}-t^

acid;

4- {6 2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin -yl acid; 4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-ethylsulfan acid;

2-Ethylsulfanyl -{6 2-(2-methyl-benzo[b]thiophen-3-yl)-ethylamino]^yrimidin -yl}-benzoic acid;

2-EthylsulfanyM-{6-[2-(2-methyl-benzofuran-3-yl)-ethylami no]-pyrimidin-4-yl}-benzoic acid;

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-pyrimidin-4-yl}-2-propy^ acid;

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-fluoro-6-m acid; 2-Chloro-4-{6-[2-(2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin^-yl}-6-m acid; (3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimidin^^^

acid;

2-Ethoxy -{6 2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin ^^ acid;

2-Ethoxy-4-{6-[2-(5-fluoro-27-dimethyl-benzo[b]thiophen-3 -yl)-ethylamino]-pyrimidin-4-y acid;

4-{6 2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin4-yl}-2-et^

4-{6-[2-(2-Bromo-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin-4-yl}-2^ acid;

4-{6-[2-(2-Chloro-5-fluoro-7-methyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin-4-yl}-^ acid; 4-{6 2-(2J imethyl-benzo[b]thiophen-3-yl)-ethylamino]^yrimidin4-yl}-2-e thoxy-benzoic acid;

2-Ethoxy-4-{6-[2-(4-fluoro-27-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin-4-^ acid;

2-Ethoxy-4-{6-[2-(6-fluoro-27-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin-4-y acid;

4-{6-[2-(4 -Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimi din-4-yl}-2-^ acid;

4-{6 2-(5-Chloro-2J-dimethyl-benzofuran-3-yl)-ethylamino]^yrimidi n4-yl}-2-ethoxy-benzoic acid;

4-{6-[2-(7-Chloro-5-fluoro-2-methyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin-4-yl}-2^ acid;

4-{6 2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]^yrimidin4- yl}-2-ethoxy-benzoic acid;

2-Ethoxy4-{6 2-(5-fluoro-2J-dimethyl-benzofuran-3-yl)-ethylamino]^yrimidi n4-yl}-benzoic acid;

4-{6 2-(5-Chloro -methoxy-2-methyl-benzofuran-3-yl)-ethylamino]^yrimidin4-yl} -2-ethoxy-benz acid;

4-{6 2-(5J ichloro-2-methyl-benzofuran-3-yl)-ethylamino]^yrimidin4-yl}- 2-ethoxy-benzoic acid;

2-Ethoxy-4-{6-[2-(2-methyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin-4-yl}-benzoic acid;

2-Ethoxy-4-{6-[2-(2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin-4-yl}-benzoic acid;

4-{6-[2-(2-chloro-benzo[b]thiophen-3-yl)-ethylamino]-pyrimid in-4-yl}-2-ethoxy-benzoic acid;

2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-1 H-indole-6-carboxylic acid;

4-{6 2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethylamino]^ yrimidin4-yl}-2-cyclopropoxy-ben acid; 2-Cyclopropoxy4-{6 2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]^yrimidin

acid; 2-Cyclopropoxy4-{6-[2-(4,5-difluoro-7-methoxy-2-methyl-benzo

acid;

4-{6-[2-(5-fluoro-2J-dimethyl-benzo[b]thio^

acid;

4-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)^thylamino]-py rimidin-4-yl}-2-propylsulfanyl-benzoic acid;

4-{6-[2-(2-Methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyri midin-4-yl}-2-propylsulfanyl-benzoic acid;

4-{6-[2-(2-Methyl-benzofuran-3-yl)-ethylamino]-pyrimidin- 4-yl}-2-propylsulfanyl-benzoic acid;

4-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)^thylamino]-py rimidin-4-yl}-2-isopropylsulfanyl-benzoic acid;

2-lsopropylsulfanyl -{6-[2-(2-methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidi n-4-yl}-benzoic acid;

2-lsopropylsulfanyl -{6-[2-(2-methyl-benzofuran-3-yl)-ethylamino]-pyrimidin-4-yl }-benzoic acid;

2-Fluoro-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidi acid; 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-isobuty acid;

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidin -yl}-2-isopropoxy-benzoi acid;

4-{6-[2-(6-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethy lamino]-pyrimidin4-yl}-2-propoxy-benzoic acid;

4-{6-[2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin4-yl}-2-propoxy-benzoic acid;

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin4-yl}-2-propoxy-benzoic acid;

4-{6-[2-(4J-Dichloro-2-methyl-benzo[b]thiophen-3-yl)^thyl amino]-pyrimidin4-yl}-2-propoxy-benzoic acid;

(4-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin4-yl}-2-ethoxy-phenyl)-acetic acid;

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidin4-yl}-2-difluorometh benzoic acid;

(4-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyr imidin-4-yl}-2-ethoxy-phen acid;

(4-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin4-yl}-2-ethoxy-phenoxy)-acetic acid;

2-Cyclobutylsulfanyl4-{6-[2-(2-methyl-benzofuran-3-yl)-et hylamino]-pyrimidin4-yl}-benzoic acid;

2-Cyclobutylsulfanyl4-{6-[2-(2J-dimethyl-benzo[b]thiophen -3-yl)-ethylamino]-pyrimidin4-yl}-benzoic aci 4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-(oxetan-3-yls^ acid; 4-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin4-yl}-2-cyclobutoxy-benzoic acid; 2-Cyclobutoxy4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]th iophen-3-yl)-ethylamino]-pyrimidin4-yl}-benzoic acid;

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidin

acid;

2-Cyclobutoxy-4-{6-[2-(4-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin acid; 4-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin4-yl}-2-cyclobutoxy-benzoic acid;

2-Cyclobutoxy4-{6-[2-(5-fluoro-2J limethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin4-yl}-b enzoi acid; 2-Cyclobutoxy4-{6-[2-(5-fluoro-2J-dimethyl-benzofuran-3-yl)^ thylamino]-pyrimidin4-yl}-benzoic acid; {6-[3-Ethoxy-4-(1 H-tetrazol-5-yl)-phenyl]-pyrimidin-4-yl}-[2-(5-fluoro-2 -dimethyl-benzo[b]thiop

amine;

3- (2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrim

acid;

2-Butoxy-6-fluoro-4-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim acid; N-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrim

acid;

2-Cyclobutoxy-3-fluoro -{6 2-(4-fluoro -methoxy-2-methyl-benzo[b]thiophen-3-yl)-ethylamino]^yrimidi benzoic acid;

2-Cyclobutoxy-4-{6-[2-(4,5-difluoro-7-methoxy-2-methyl-be nzofuran-3-yl)-ethylamino]-pyrimidin

benzoic acid;

4- {6 2-(5-Chloro -methoxy-2-methyl-benzofuran-3-yl)-ethylamino]^yrimidin-4-yl }-2-cyclobutoxy-6-fluoro-benzoic acid;

2- Cyclopentyloxy -{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin -yl}-benzoic acid; 2-Cyclopentyloxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzofuran-3 -yl)-ethylamino]-pyrimidin-4-yl}-benzoic acid;

3- (2-Ethoxy -{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin-4-yl}-phenyl)-

[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(2-ethoxy-4-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen- 3- yl)ethyl)amino)pyrimidin-4-yl)phenyl)-[1 ,2,4]oxadiazol-5-ol];

3- Ethoxy-5-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl) ethyl)amino)pyrimidin

2-carboxamide;

4- Ethyl-2-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimi

acid; and

3- (4-Ethyl-2-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim

[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(4-ethyl-2-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3 - yl)ethyl)amino)pyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol].

30) Another embodiment relates to compounds of formula (I) as defined in embodiment 1 ) for use according to embodiment 1 ) which are selected from the compounds according to embodiments 28) and/or 29).

31 ) In addition to the compounds listed in embodiments 28) and 29), further compounds of formula (II) according to embodiment 8), are selected from the following compounds:

(4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidi

acetic acid;

4- {6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-ethy lamino]-pyrimidin-4-yl}-2-propyl-benzoic acid; (4-{6 2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-ethylami no]^yrimidin-4-yl}-2-methoxy-phenyl)-acetic acid; (4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin-4-yl}-2-propoxy

acid;

(4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin -yl}-2-prop

acid;

(4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin -yl}-2-iso

acetic acid;

4- {6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-ethy lamino]-pyrimidin-4-yl}-2-isopropoxy-benz acid; 3-(4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl) -ethylamino]-pyrimidin-4-yl}-2-ethoxy-phenoxy)- propionic acid;

2-Ethylsulfanyl-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]th iophen-3-yl)-ethylamino]-pyrim acid; 3-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-pyrimidin-4-yl}- ene-1 ,2-dione;

(4-{6-[2-(5-Fluoro-2J limethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin -yl}-2-i acid; (2-Ethyl-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimidi acid; (2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimi

acid;

(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyl amino]-pyrimidin-4-y acid; N-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimi

(2-Ethyl-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimi

acid;

2-Cyclopropoxy-4-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim acid;

(2-Cyclopropoxy-4-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimi

acid;

(3-Ethyl-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pyrimi

acid;

(2-Chloro-4-{6-[2-(5-fluorO-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimi

acetic acid;

5- (2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-pyrimidi

[tautomeric form: 5-(2-ethoxy -(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethyl)am ino)pyrimidin-4- yl)phenyl)isoxazol-3(2H)-one];

1-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimi

cyclopropanecarboxylic acid; and

1-(4-{6 2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]^y rimidin-4-yl}-2-propyl-phenyl)- cyclopropanecarboxylic acid. 32) In addition to the compounds listed in embodiments 28), 29), and 31 ), further compounds of formula (II) according to embodiment 8), are selected from the following compounds:

4-{6 2-(2,7 imethyl-benzo[b]thiophen-3-yl)-ethylamino]^yrimidin -yl}-2-isobutylsulfanyl-benzoic acid;

4-{6-[2-(2-Cyano-benzo[b]thiophen-3-yl)-ethylamino]-pyrim idin-4-yl}-2-methylsulfanyl-benzoic acid;

(4-{6-[2-(2-Cyano-benzo[b]thiophen-3-yl)-ethylamino]-pyri midin-4-yl}-2-ethoxy-phenyl)-acetic acid;

3- (4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-phenyl)-[1 ,2,4]oxadiazol- 5(4H)-one [tautomeric form: 3-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-pyrimidin-4-yl}- phenyl)-[1 ,2,4]oxadiazol-5-ol];

4- {6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin-4-yl}-benzamide;

[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyl]-[ 6-(1 H-indol-5-yl)-pyrimidin-4-yl]-amine;

4- {6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-2-isobutoxy-benzoic acid; (4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-2-propyl-phenyl)-acetic acid; (4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]^ yhmidin -yl}-2 hfluoromethoxy-phenyl)- acetic acid;

N-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-4-yl}-phenyl)-formamide;

(4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]^ yrimidin -yl}-2-isopropoxy-phenyl)-acetic acid;

2-Ethyl-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyhmidin -yl}-benzoic acid;

5- (4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]^ yrimidin -yl}-2-methoxy-phenyl)-isoxazol- 3-ol [tautomeric form: 5-(4-(6-((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethy l)amino)pyrimidin-4-yl)-2- methoxyphenyl)isoxazol-3(2H)-one];

5-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-2-methyl-1 H-pyrrole-3- carboxylic acid;

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-propyl-benzamide;

4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-N-(2-hydroxy-2-methyl-propyl)- 2-propyl-benzamide;

4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-N-(2-methoxy-ethyl)-2-propyl- benzamide;

4-{6 2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]- pyrimidin-4-yl}-N-(2-hydroxy-ethyl)-2-propyl- benzamide;

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin4-yl}-N-methyl-2-propyl-benzamide;

2-Ethoxy4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3 -yl)-ethylamino]-pyrimidin4-yl}-N-(2-hydroxy-ethyl)- benzamide;

2-Ethoxy4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin4-yl}-N-methyl-benzamide; 2-Ethoxy4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin4-yl}-benzamide; (2-Ethoxy-3-fluoro-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]th iophen-3-yl)-ethylamin

acid;

(5-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyl amino]-pyrimidin-^

acid;

(3-Difluoromethoxy-5-{6-[2-(5-fluoro-2J-dimethyl-benzo[b] thiophen-3-yl)-ethylami

yl)-acetic acid;

2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-1 H-indole-7-carboxylic acid;

2- {6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin-4-yl}-ben

acid; and

3-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-4-yl^

acid.

33) In addition to the compounds listed in embodiments 28), 29), 31 ) and 32), a further compound of formula (II) according to embodiment 8) is:

(4-{6 2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino]^yrim idin-4-yl}-2-ethoxy-phenyl)-acetic acid. 34) Another embodiment relates to compounds of formula (I) as defined in embodiment 1 ) for use according to embodiment 1 ) which are selected from the compounds according to embodiments 31 to 33); as well as the following compounds:

3- Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl) -ethylamino]-pyrimid H-pyrrole-2-carboxylic acid;

1-Ethyl-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3 -yl)-ethylamino]-pyrimi H-pyrrole-2-carboxylic acid; and

4- {6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin-4-yl}-1 -propyl- acid.

The compounds of formula (I) / formula (II) according to embodiments 1 ) to 34) and their pharmaceutically acceptable salts can be used as medicaments, e.g. in the form of pharmaceutical compositions for enteral (such especially oral e.g. in form of a tablet or a capsule) or parenteral administration (including topical application or inhalation).

The production of the pharmaceutical compositions can be effected in a manner which will be familiar to any person skilled in the art (see for example Remington, The Science and Practice of Pharmacy, 21 st Edition (2005), Part 5, "Pharmaceutical Manufacturing" [published by Lippincott Williams & Wilkins]) by bringing the described compounds of formula (I) / formula (II) or their pharmaceutically acceptable salts, optionally in combination with other therapeutically valuable substances, into a galenical administration form together with suitable, non-toxic, inert, therapeutically compatible solid or liquid carrier materials and, if desired, usual pharmaceutical adjuvants. The present invention also relates to a method for the prevention / prophylaxis or treatment of a disease or disorder mentioned herein comprising administering to a subject a pharmaceutically active amount of a compound of formula (I) / formula (II) according to embodiments 1 ) to 34).

In a preferred embodiment of the invention, the administered amount is comprised between 1 mg and 2000 mg per day, particularly between 5 mg and 1000 mg per day, more particularly between 25 mg and 500 mg per day, especially between 50 mg and 200 mg per day.

Whenever the word "between" is used to describe a numerical range, it is to be understood that the end points of the indicated range are explicitly included in the range. For example: if a temperature range is described to be between 40 °C and 80 °C, this means that the end points 40 °C and 80 °C are included in the range; or if a variable is defined as being an integer between 1 and 4, this means that the variable is the integer 1 , 2, 3, or 4.

Unless used regarding temperatures, the term "about" placed before a numerical value "X" refers in the current application to an interval extending from X minus 10% of X to X plus 10% of X, and preferably to an interval extending from X minus 5% of X to X plus 5% of X. In the particular case of temperatures, the term "about" placed before a temperature "Y" refers in the current application to an interval extending from the temperature Y minus 10 °C to Y plus 10 °C, and preferably to an interval extending from Y minus 5 °C to Y plus 5 °C.

For avoidance of any doubt, if compounds are described as useful for the prevention / prophylaxis or treatment of certain diseases, such compounds are likewise suitable for use in the preparation of a medicament for the prevention / prophylaxis or treatment of said diseases. Likewise, such compounds are also suitable in a method for the prevention / prophylaxis or treatment of such diseases, comprising administering to a subject (mammal, especially human) in need thereof, an effective amount of such compound.

The compounds of formula (I) / formula (II) according to embodiments 1 ) to 34) are useful for the prevention / prophylaxis or treatment of disorders relating to the EP2 and/or EP4 receptors.

Certain compounds of formula (I) / formula (II) according to embodiments 1 ) to 34) exhibit their biological activity as modulators of the prostaglandin 2 receptors EP2 and/or EP4 in a biological environment, (i.e. in the presence of one or more enzymes capable of breaking a covalent bond linked to a carbonyl group such as an amidase, an esterase or any suitable equivalent thereof capable of removing a prodrug group from a carboxylic acid group.

Diseases or disorders relating to the EP2 and/or EP4 receptors are especially

• cancer (notably melanoma including metastatic melanoma; lung cancer including non-small cell lung cancer; bladder cancer including urinary bladder cancer, urothelial cell carcinoma; renal carcinomas including renal cell carcinoma, metastatic renal cell carcinoma, metastatic renal clear cell carcinoma; gastro-intestinal cancers including colorectal cancer, metastatic colorectal cancer, familial adenomatous polyposis (FAP), oesophageal cancer, gastric cancer, gallbladder cancer, cholangiocarcinoma, hepatocellular carcinoma, and pancreatic cancer such as pancreatic adenocarcinoma or pancreatic ductal carcinoma; endometrial cancer; ovarian cancer; cervical cancer; neuroblastoma; prostate cancer including castrate-resistant prostate cancer; brain tumors including brain metastases, malignant gliomas, glioblastoma multiforme, medulloblastoma, meningiomas; breast cancer including triple negative breast carcinoma; oral tumors; nasopharyngeal tumors; thoracic cancer; head and neck cancer; leukemias including acute myeloid leukemia, adult T-cell leukemia; carcinomas; adenocarcinomas; thyroid carcinoma including papillary thyroid carcinoma; choriocarcinoma; Ewing's sarcoma; osteosarcoma; rhabdomyosarcoma; Kaposi's sarcoma; lymphoma including Burkitt's lymphoma, Hodgkin's lymphoma, MALT lymphoma; multiple myelomas; and virally induced tumors; especially melanoma; lung cancer; bladder cancer; renal carcinomas; gastro-intestinal cancers; endometrial cancer; ovarian cancer; cervical cancer; and neuroblastoma);

as well as further diseases or disorders relating to the EP2 and/or EP4 receptors such as:

pain (notably inflammatory pain and painful menstruation);

endometriosis;

autosomal dominant polycystic kidney disease;

acute ischemic syndromes in atherosclerotic patients;

pneumonia; and

• neurodegenerative diseases including amyotrophic lateral sclerosis, stroke; Parkinson disease, Alzheimer's disease and H IV associated dementia;

• and EP2 and/or EP4 antagonists may further be used to control female fertility.

Further diseases or disorders relating to the EP2 and/or EP4 receptors are autoimmune disorders such as especially multiple sclerosis, rheumatoid arthritis and osteoarthritis; and osteoporosis.

The compounds of formula (I) / formula (II) according to any one of embodiments 1 ) to 34) are in particular useful as therapeutic agents for the prevention / prophylaxis or treatment of a cancer. They can be used as single therapeutic agents or in combination with one or more chemotherapy agents and / or radiotherapy and / or targeted therapy. Such combined treatment may be effected simultaneously, separately, or over a period of time.

The invention, thus, also relates to pharmaceutical compositions comprising a pharmaceutically acceptable carrier material, and:

• a compound of formula (I) / formula (II) according to any one of embodiments 1 ) to 34);

• and one or more cytotoxic chemotherapy agents.

The invention, thus, further relates to a kit comprising

· a pharmaceutical composition, said composition comprising a pharmaceutically acceptable carrier material, and:

> a compound of formula (I) / formula (II) according to any one of embodiments 1 ) to 34);

• and instructions how to use said pharmaceutical composition for the prevention / prophylaxis or the treatment of a cancer, in combination with chemotherapy and / or radiotherapy and / or targeted therapy. The terms "radiotherapy" or "radiation therapy" or "radiation oncology", refer to the medical use of ionizing radiation in the prevention / prophylaxis (adjuvant therapy) and / or treatment of cancer; including external and internal radiotherapy.

The term "targeted therapy" refers to the prevention / prophylaxis (adjuvant therapy) and / or treatment of cancer with one or more anti-neoplastic agents such as small molecules or antibodies which act on specific types of cancer cells or stromal cells. Some targeted therapies block the action of certain enzymes, proteins, or other molecules involved in the growth and spread of cancer cells. Other types of targeted therapies help the immune system kill cancer cells (immunotherapies); or inhibit angiogenesis, the growth and formation of new blood vessels in the tumor; or deliver toxic substances directly to cancer cells and kill them. An example of a targeted therapy which is in particular suitable to be combined with the compounds of the present invention is immunotherapy, especially immunotherapy targeting the progammed cell death receptor 1 (PD-1 receptor) or its ligand PD-L1 (Zelenay et al., 2015, Cell 162, 1 -14; Yongkui Li et al., Oncoimmunology 2016, 5(2):e1074374).

When used in combination with the compounds of formula (I) / formula (II), the term "targeted therapy" especially refers to agents such as:

a) Epidermal growth factor receptor (EGFR) inhibitors or blocking antibodies (for example Gefitinib, Erlotinib, Afatinib, lcotinib, Lapatinib, Panitumumab, Zalutumumab, Nimotuzumab, Matuzumab and Cetuximab); b) RAS/RAF/MEK pathway inhibitors (for example Vemurafenib, Sorafenib, Dabrafenib,GDC-0879, PLX- 4720, LGX818, RG7304, Trametinib (GSK1120212), Cobimetinib (GDC-0973/XL518), Binimetinib (MEK162, ARRY-162), Selumetinib (AZD6244));

c) Aromatase inhibitors (for example Exemestane, Letrozole, Anastrozole, Vorozole, Formestane, Fadrozole);

d) Angiogenesis inhibitors, especially VEGF signalling inhibitors such as Bevacuzimab (Avastin), Ramucirumab , Sorafenib or Axitinib;

e) Immune Checkpoint inhibitors (for example: anti-PD1 antibodies such as Pembrolizumab (Lambrolizumab, MK-3475), Nivolumab, Pidilizumab (CT-011 ), AMP-514/MED10680, PDR001 , SHR-1210; REGN2810, BGBA317; fusion proteins targeting PD-1 such as AMP-224; small molecule anti-PD1 agents such as for example compounds disclosed in WO2015/033299, WO2015/044900 and WO2015/034820; anti-PD1 L antibodies, such as BMS-936559, atezolizumab (MPDL3280A, RG7446), MEDI4736, avelumab (MSB0010718C), durvalumab (MEDI4736); anti-PDL2 antibodies, such as AMP224; anti-CTLA-4 antibodies, such as ipilimumab, tremilmumab; anti-Lymphocyte-activation gene 3 (LAG-3) antibodies, such as BMS-986016, IMP701 , MK-4280, ImmuFact IMP321 ; anti T cell immunoglobulin mucin-3 (TIM-3) antibodies, such as MBG453; anti-CD137/4-1 BB antibodies, such as BMS-663513 / urelumab, PF- 05082566; anti T cell immunoreceptorwith Ig and ITIM domains (TIG IT) antibodies, such as RG6058 (anti- TIGIT, MTIG7192A); f) Vaccination approaches (for example dendritic cell vaccination, peptide or protein vaccination (for example with gp100 peptide or MAGE-A3 peptide);

g) Re-introduction of patient derived or allogenic (non-self) cancer cells genetically modified to secrete immunomodulatory factors such as granulocyte monocyte colony stimulating factor (GMCSF) gene- transfected tumor cell vaccine (GVAX) or Fms-related tyrosine kinase 3 (Flt-3) ligand gene-transfected tumor cell vaccine (FVAX),or Toll like receptor enhanced GM-CSF tumor based vaccine (TEGVAX); h) T-cell based adoptive immunotherapies, including chimeric antigen receptor (CAR) engineered T-cells (for example CTL019);

i) Cytokine or immunocytokine based therapy (for example Interferon alpha, interferon beta, interferon gamma, interleukin 2, interleukin 15);

j) Toll-like receptor (TLR) agonists (for example resiquimod, imiquimod, glucopyranosyl lipid A, CpG oligodesoxynucleotides);

k) Thalidomide analogues (for example Lenalidomide, Pomalidomide);

I) lndoleamin-2,3-Dioxgenase (IDO) and/or Tryptophane-2,3-Dioxygenase (TDO) inhibitors (for example RG6078 / NLG919 / GDC-0919; Indoximod / 1 MT (1 -mefhyltryptophan), INCB024360 / Epacadostat, PF- 06840003 (EOS200271 ), F001287);

m) Activators of T-cell co-stimulatory receptors (for example anti-OX40/CD134 (Tumor necrosis factor receptor superfamily, member 4, such as RG7888 (MOXR0916), 9B12; MEDI6469, GSK3174998, MEDI0562), anti OX40-Ligand/CD252; anti-glucocorticoid-induced TNFR family related gene (GITR) (such as TRX518, MEDI1873, MK-4166, BMS-986156), anti-CD40 (TNF receptor superfamily member 5) antibodies (such as Dacetuzumab (SGN-40), HCD122, CP-870,893, RG7876, ADC-1013, APX005M, SEA-CD40); anti-CD40-Ligand antibodies (such as BG9588); anti-CD27 antibodies such as Varlilumab); n) Molecules binding a tumor specific antigen as well as a T-cell surface marker such as bispecific antibodies (for example RG7802 targeting CEA and CD3) or antibody fragments, antibody mimetic proteins such as designed ankyrin repeat proteins (DARPINS), bispecific T-cell engager (BITE, for example AMG103, AMG330);

o) Antibodies or small molecular weight inhibitors targeting colony-stimulating factor- 1 receptor (CSF-1 R) (for example Emactuzumab (RG7155), Cabiralizumab (FPA-008), PLX3397);

p) Agents targeting immune cell check points on natural killer cells such as antibodies against Killer-cell immunoglobulin-like receptors (KIR) for example Lirilumab (IPH2102/BMS-986015);

q) Agents targeting the Adenosine receptors or the ectonucleases CD39 and CD73 that convert ATP to

Adenosine, such as MEDI9447 (anti-CD73 antibody), PBF-509; CPI-444 (Adenosine A2a receptor antagonist).

When used in combination with the compounds of formula (I) / formula (II), immune checkpoint inhibitors such as those listed under d), and especially those targeting the progammed cell death receptor 1 (PD-1 receptor) or its ligand PD-L1 , are preferred. The term "chemotherapy" refers to the treatment of cancer with one or more cytotoxic anti-neoplastic agents ("cytotoxic chemotherapy agents"). Chemotherapy is often used in conjunction with other cancer treatments, such as radiation therapy or surgery. The term especially refers to conventional cytotoxic chemotherapeutic agents which act by killing cells that divide rapidly, one of the main properties of most cancer cells. Chemotherapy may use one drug at a time (single-agent chemotherapy) or several drugs at once (combination chemotherapy or polychemotherapy). Chemotherapy using drugs that convert to cytotoxic activity only upon light exposure is called photochemotherapy or photodynamic therapy.

The term "cytotoxic chemotherapy agent" or "chemotherapy agent" as used herein refers to an active anti-neoplastic agent inducing apoptosis or necrotic cell death. When used in combination with the compounds of formula (I) / formula (II), the term especially refers to conventional cytotoxic chemotherapy agents such as:

a) alkylating agents (for example mechlorethamine, chlorambucil, cyclophosphamide, ifosfamide, streptozocin, carmustine, lomustine, melphalan, dacarbazine, temozolomide, fotemustine, thiotepa or altretamine; especially cyclophosphamide, carmustine, melphalan, dacarbazine, or temozolomide);

b) platinum drugs (especially cisplatin, carboplatin or oxaliplatin);

c) antimetabolite drugs (for example 5-fluorouracil, folic acid/leucovorin, capecitabine, 6-mercaptopurine, methotrexate, gemcitabine, cytarabine, fludarabine or pemetrexed; especially 5-fluorouracil, folic acid/leucovorin, capecitabine, methotrexate, gemcitabine or pemetrexed);

d) anti-tumor antibiotics (for example daunorubicin, doxorubicin, epirubicin, idarubicin, actinomycin-D, bleomycin, mitomycin-C or mitoxantrone; especially doxorubicin);

e) mitotic inhibitors (for example paclitaxel, docetaxel, ixabepilone, vinblastine, vincristine, vinorelbine, vindesine or estramustine; especially paclitaxel, docetaxel, ixabepilone or, vincristine); or

f) topoisomerase inhibitors (for example etoposide, teniposide, topotecan, irinotecan, diflomotecan or elomotecan; especially etoposide or irinotecan).

When used in combination with the compounds of formula (I) /formula (II), preferred cytotoxic chemotherapy agents are the above-mentioned alkylating agents (notably fotemustine,cyclophosphamide, ifosfamide, carmustine, dacarbazine and prodrugs thereof such as especially temozolomide or pharmaceutically acceptable salts of these compounds; in particular temozolomide); mitotic inhibitors (notably paclitaxel, docetaxel, ixabepilone,; or pharmaceutically acceptable salts of these compounds; in particular paclitaxel); platinum drugs (notably cisplatin, oxaliplatin and carboplatin); as well etoposide and gemcitabine.

Chemotherapy may be given with a curative intent or it may aim to prolong life or to palliate symptoms.

• Combined modality chemotherapy is the use of drugs with other cancer treatments, such as radiation therapy or surgery.

• Induction chemotherapy is the first line treatment of cancer with a chemotherapeutic drug. This type of chemotherapy is used for curative intent. • Consolidation chemotherapy is the given after remission in order to prolong the overall disease free time and improve overall survival. The drug that is administered is the same as the drug that achieved remission.

• Intensification chemotherapy is identical to consolidation chemotherapy but a different drug than the induction chemotherapy is used.

• Combination chemotherapy involves treating a patient with a number of different drugs simultaneously.

The drugs differ in their mechanism and side effects. The biggest advantage is minimising the chances of resistance developing to any one agent. Also, the drugs can often be used at lower doses, reducing toxicity.

· Neoadjuvant chemotherapy is given prior to a local treatment such as surgery, and is designed to shrink the primary tumor. It is also given to cancers with a high risk of micrometastatic disease.

• Adjuvant chemotherapy is given after a local treatment (radiotherapy or surgery). It can be used when there is little evidence of cancer present, but there is risk of recurrence. It is also useful in killing any cancerous cells that have spread to other parts of the body. These micrometastases can be treated with adjuvant chemotherapy and can reduce relapse rates caused by these disseminated cells.

• Maintenance chemotherapy is a repeated low-dose treatment to prolong remission.

• Salvage chemotherapy or palliative chemotherapy is given without curative intent, but simply to decrease tumor load and increase life expectancy. For these regimens, a better toxicity profile is generally expected.

"Simultaneously", when referring to an administration type, means in the present application that the administration type concerned consists in the administration of two or more active ingredients and/or treatments at approximately the same time; wherein it is understood that a simultaneous administration will lead to exposure of the subject to the two or more active ingredients and/or treatments at the same time. When administered simultaneously, said two or more active ingredients may be administered in a fixed dose combination, or in an equivalent non-fixed dose combination (e.g. by using two or more different pharmaceutical compositions to be administered by the same route of administration at approximately the same time), or by a non-fixed dose combination using two or more different routes of administration; wherein said administration leads to essentially simultaneous exposure of the subject to the two or more active ingredients and/or treatments. For example, when used in combination with chemotherapy and/or suitable targeted therapy, the present EP2/EP4 antagonists would possibly be used "simultaneously".

"Fixed dose combination", when referring to an administration type, means in the present application that the administration type concerned consists in the administration of one single pharmaceutical composition comprising the two or more active ingredients.

"Separately", when referring to an administration type, means in the present application that the administration type concerned consists in the administration of two or more active ingredients and/or treatments at different points in time; wherein it is understood that a separate administration will lead to a treatment phase (e.g. at least 1 hour, notably at least 6 hours, especially at least 12 hours) where the subject is exposed to the two or more active ingredients and/or treatments at the same time; but a separate administration may also lead to a treatment phase where for a certain period of time (e.g. at least 12 hours, especially at least one day) the subject is exposed to only one of the two or more active ingredients and/or treatments. Separate administration especially refers to situations wherein at least one of the active ingredients and/or treatments is given with a periodicity substantially different from daily (such as once or twice daily) administration (e.g. wherein one active ingredient and/or treatment is given e.g. once or twice a day, and another is given e.g. every other day, or once a week or at even longer distances). For example, when used in combination with radiotherapy, the present EP2/EP4 antagonists would possibly be used "separately".

By administration "over a period of time" is meant in the present application the subsequent administration of two or more active ingredients and/or treatments at different times. The term in particular refers to an administration method according to which the entire administration of one of the active ingredients and/or treatments is completed before the administration of the other / the others begins. In this way it is possible to administer one of the active ingredients and/or treatments for several months before administering the other active ingredient(s) and/or treatment(s).

Administration "over a period of time" also encompasses situations wherein the compound of formula (I) / formula (II) would be used in a treatment that starts after termination of an initial chemotherapeutic (for example an induction chemotherapy) and/or radiotherapeutic treatment and/or targeted therapy treatment, wherein optionally said treatment would be in combination with a further / an ongoing chemotherapeutic and/or radiotherapeutic treatment and/or targeted therapy treatment (for example in combination with a consolidation chemotherapy, an intensification chemotherapy, an adjuvant chemotherapy, or a maintenance chemotherapy; or radiotherapeutic equivalents thereof); wherein such further / ongoing chemotherapeutic and/or radiotherapeutic treatment and/or targeted therapy treatment would be simultaneously, separately, or over a period of time in the sense of "not given with the same periodicity".

The compounds of formula (I) / formula (II) as defined in embodiments 1 ) to 34) are also useful in a method of modulating an immune response in a subject having a tumor, comprising the administration of an effective amount of the compound of formula (I) / formula (II) [wherein notably said administration of said effective amount results in the pharmacologically active blockage of the EP2 receptors, or of the EP4 receptors, or of both the EP2 and the EP4 receptors]; wherein said effective amount reactivates the immune system in the tumor of said subject; wherein especially said effective amount:

· counteracts the polarization of tumor-associated macrophages towards tumor-promoting M2 macrophages; and/or

• down-regulates the activation, expansion and/or the effector function of immunosuppressive cells that have accumulated in a tumor (especially of regulatory T cells (Tregs) and/or myeloid derived suppressor cells (MDSC)); and/or • up-regulates IFN-γ and/or TNF-a and/or IL-12 and/or IL-2 expression in immune cells such as natural killer cells, T-cells, dendritic cells and macrophages (leading to the induction of tumor cell apoptosis and/or restrained tumorigenesis); and/or

• directly or indirectly counteracts the suppressed activation, IL-2 responsiveness and expansion of cytotoxic T- cells (thereby decreasing local immunsuppression).

The compounds of formula (I) / formula (II) as defined in embodiments 1 ) to 34) are also useful in a method of diminishing tumor growth and/or reducing tumor size in a subject having a tumor, comprising the administration of an effective amount of the compound of formula (I) /formula (II) [wherein notably said administration of said effective amount results in the pharmacologically active blockage of the EP2 receptors, or of the EP4 receptors, or of both the EP2 and the EP4 receptors]; wherein said effective amount down-regulates tumor angiogenesis (especially by decreasing endothelial cell motility and/or survival, and/or by decreasing the expression of VEGF (vascular endothelial growth factor)); and/or wherein said effective amount diminishes tumor cell survival and/or induces tumor cell apoptosis (especially via inhibition of PI3K/AKT and MAPK signalling).

The compounds of formula (I) / formula (II) as defined in embodiments 1 ) to 34) are also useful in a method of modulating an immmune response in a subject having a tumor, comprising the administration of an effective amount of the compound of formula (I) / formula (II) [wherein notably said administration of said effective amount results in the pharmacologically active blockage of the EP2 receptors, or of the EP4 receptors, or of both the EP2 and the EP4 receptors]; wherein said effective amount reactivates the immune system in the tumor of said subject; wherein said effective amount activates the cytotoxicity and cytokine production of natural killer cells and/or cytotoxic T- cells.

Besides, any preferences and (sub-)embodiments indicated for the compounds of formula (II) (whether for the compounds themselves, salts thereof, compositions containing the compounds or salts thereof, or uses of the compounds or salts thereof, etc.) apply mutatis mutandis to compounds of formula (I).

Preparation of compounds of formula (I):

The compounds of formula (I) / formula (II) can be prepared by well-known literature methods, by the methods given below, by the methods given in the experimental part below or by analogous methods. Optimum reaction conditions may vary with the particular reactants or solvents used, but such conditions can be determined by a person skilled in the art by routine optimisation procedures. In some cases the order of carrying out the following reaction schemes, and/or reaction steps, may be varied to facilitate the reaction or to avoid unwanted reaction products. In the general sequence of reactions outlined below, the generic groups R ¹ , R ² , R ³ , R ^4a , R ^4b , R ^5a , R ^5b and Ar ¹ are as defined for formula (I). Other abbreviations used herein are explicitly defined, or are as defined in the experimental section. In some instances the generic groups R ¹ , R ² , R ³ , R ^4a , R ^4b , R ^5a , R ^5b and Ar ¹ might be incompatible with the assembly illustrated in the schemes below and so will require the use of protecting groups (PG). The use of protecting groups is well known in the art (see for example "Protective Groups in Organic Synthesis", T.W. Greene, P.G.M. Wuts, Wiley-lnterscience, 1999). For the purposes of this discussion, it will be assumed that such protecting groups as necessary are in place. In some cases the final product may be further modified, for example, by manipulation of substituents to give a new final product. These manipulations may include, but are not limited to, reduction, oxidation, alkylation, acylation, hydrolysis and transition-metal catalysed cross-coupling reactions which are commonly known to those skilled in the art. The compounds obtained may also be converted into salts, especially pharmaceutically acceptable salts, in a manner known per se.

Compounds of formula (I) / formula (II) of the present invention can be prepared according to the general sequence of reactions outlined below.

A general synthetic route allowing the preparation of compounds of formula (I) is presented in scheme 1. Thus, precursors A3 can be obtained by nucleophilic aromatic substitutions between primary amines A1 and pyrimidine halides A2 (wherein X is a chlorine, a bromine or an iodine), in the presence of a base such as TEA, DIPEA or K2CO3, in a solvent such as isopropanol, butanol, DMF or THF, at RT or at elevated temperatures. Compounds of formula (I) can be produced via Suzuki cross-coupling reactions of the pyrimidine halides A3 with boronic acids or boronate esters A4. Typical Suzuki cross-coupling reactions may be carried out in the presence of a base such as K2CO3, CS2CO3, Na ₂ C0 ₃ , K3PO4, or CsF and a catalyst such as Pd(PPh ₃ ) ₄ , Pd(dppf)CI ₂ or Pd(OAc) ₂ , in a solvent like ethanol, THF, water, or mixtures thereof, typically at elevated temperatures. Boronic acids or boronate esters A4 can be obtained from commercial sources, or synthesized by methods described in the literature, or by methods known by a person skilled in the art. A boronic acid derivative can be formed by the Miyaura borylation reaction, by cross-coupling of bis(pinacolato)diboron with aryl halides or triflates, in the presence of a base such as potassium acetate and a catalyst such as Pd(dppf)Cl2. Alternatively, a boronic acid derivative can be formed by a lithiation/borylation sequence, typically at low temperatures, using butyllithium or lithium diisopropylamide as the base, and tri-isopropylborate or isopropoxyboronic acid pinacol ester, in a solvent such as diethyl ether or THF. In a variant, compounds of formula (I) can be prepared via nucleophilic aromatic substitutions between primary amines A1 and substituted pyrimidine halides A5, wherein X is a chlorine, a bromine or an iodine {scheme 1).

Scheme 1. General preparations of compounds of formula (I); in scheme 1, X represents CI, Br or I.

Alternatively, compounds of formula (I) can be synthesized by reacting a compound of formula A1 with a compound of formula A5 wherein X represents OH, in presence of a coupling agent such as (benzotriazol-1 -yloxy)- tris(dimethylamino)-phosphonium hexafluorophosphate (BOP), (benzotriazol-1 -yl-oxy)-tripyrrolidino-phosphonium hexafluorophosphate (PyBOP) or hexachlorocyclotriphosphazene, in presence of a base such as DBU, DIPEA or TEA in a solvent such as THF, MeCN or DMF, at low temperatures, or at RT or at elevated temperatures.

Substituted benzothiophenes corresponding to compounds of formula (I) (with R ² representing CN) can be prepared according to the synthetic route described in scheme 2. Ortho-fluorobenzonitriles or ortho-chlorobenzonitriles B1 can undergo aromatic nucleophilic substitutions by treatment with methyl 2-mercaptoacetate in the presence of a base (K2CO3/DMF), and benzothiophenes B2 can be obtained after a subsequent ring closure. The related 3- bromobenzothiophenes B3 can be obtained via deaminative bromination (tert-butyl n i tri te/cop pe r( 11 ) bromide/MeCN), and alkaline hydrolysis of the ester functionality in B3 followed by coupling of the corresponding acid chlorides with ammonium hydroxide can provide primary amides B4. A dehydration of the primary amide moiety in B4 (cyanuric chloride//DMF) can furnish the benzo[b]thiophene-2-carbonitrile derivatives B5. A subsequent Suzuki-Miyaura aminoethylation [Pd(OAc)2/RuPhos/Cs2C03/toluene/H ₂ 0] of bromobenzothiophenes B5 using Boc-protected potassium β-aminoethyltrifluoroborates B6 can furnish derivatives B7 that can be converted to primary amines B8 after Boc-deprotection under acidic conditions. Finally, target products B9 corresponding to compounds of formula (I) can be obtained from B8 with the preparations described in scheme 1.

Scheme 2. Preparation of substituted benzothiophenes B9 corresponding to compounds of formula (I) with X representing S and R ² representing CN; in scheme 2, Hal represents F or CI.

Substituted benzothiophenes corresponding to compounds of formula (I) (with R ² representing Me) can be prepared according to the synthetic route described in scheme 3. This multi-step synthesis started with the preparation of 2- methylbenzothiophenes C3 via a thio-Claisen rearrangement. Thus, S-alkylation of thiophenols C1 by treatment with 2,3-dichloropropene in the presence of potassium carbonate can introduce the required 2-chloropropene moiety in derivatives C2. A subsequent thio-Claisen rearrangement in refluxing Ν,Ν-diethylaniline can convert the S-alkylated derivatives C2 into the target 2-methylbenzothiophenes C3. The aldehyde functionality can be introduced at the unsubstituted 3-position via selective formylation of the thiophene ring under mild conditions (dichloromethyl methyl ether/tin(IV) chloride) affording compounds C4. The β-aminoethyl side-chain in C5 can result from the reduction (lithium aluminum hydride/THF/heating) of the corresponding nitroalkenes that can be prepared from aldehydes C4 via Henry reaction (nitromethane/butylamine/acetic acid/heating). Finally, target products C6 corresponding to compounds of formula (I) can be obtained according to the sequences described in scheme 1.

Scheme 3. Preparation of substituted benzothiophenes C6 corresponding to compounds of formula (I) with X representing S and R ² representing Me.

Substituted benzothiophenes corresponding to compounds of formula (I) (with R ² representing CI or Br) can be prepared according to the sequence of reactions described in scheme 2. This multi-step synthesis started with the preparation of 2-unsubstituted benzothiophenes D6 as precursors for the planned halogenation at position-2. Thus, S-alkylation of thiophenols D1 (methyl bromoacetate/potassium carbonate) followed by alkaline hydrolysis of the ester functionality can provide the 2-(phenylthio)acetic acid derivatives D2. Conversion of the carboxylic acids D2 into the corresponding acid chlorides, and subsequent Friedel-Crafts acylation (aluminum chloride/DCM) can deliver benzo[b]thiophen-3(2H)-ones D3. The substituted benzothiophenes D4 can be obtained via Wittig olefination of D3 [(carbethoxymethylene)triphenylphosphorane/toluene/reflux], and the protected β-aminoethyl side-chain in D6 can result from the reduction of the ester functionality in D4 followed by reaction of the resulting primary alcohols D5 with phthalimide under Mitsunobu conditions (diethyl azodicarboxylate/triphenylphosphine/THF). A subsequent regioselective chlorination (N- chlorosuccinimide/DMF/heating) or bromination (N-bromosuccinimide/DMF/heating) of the unsubstituted 2-position of the thiophene ring in D6 can deliver the corresponding derivatives D7, and primary amines D8 can be obtained after cleavage of the phthalimide moiety (hydrazine hydrate/MeOH/heating). Finally, target products D9 corresponding to compounds of formula (I) can be obtained from D8 with the sequence of reactions described in scheme 1.

Scheme 4. Preparation of substituted benzothiophenes D9 corresponding to compounds of formula (I) with X representing S and R ² representing CI or Br.

Substituted benzofurans corresponding to compounds of formula (I) [with R ² representing can be prepared according to the synthetic route shown in scheme 5. Ortho-hydroxybenzaldehydes E1 can be converted to the corresponding carboxylic acids E2 via O-alkylation with the appropriate electrophile followed by saponification of the ester functionality. Subsequent heating of the produced carboxylic acids E2 with sodium acetate in acetic anhydride can deliver the substituted benzofurans E3. The aldehyde functionality in E4 can be introduced at the unsubstituted 3-position of benzofurans E3 via regioselective formylation of the furan ring under mild conditions (dichloromethyl methyl ether/tin(IV) chloride). The β-aminoethyl side-chain in E5 can result from the reduction of the corresponding nitroalkenes that can be prepared from aldehydes E4 via Henry reaction (nitromethane/butylamine/acetic acid). Finally, target products E6 corresponding to compounds of formula (I) can be obtained with the sequence of reactions described in scheme 1.

Scheme 5. Preparation of substituted benzofurans E6 corresponding to compounds of formula (I) with X representing 0 and R ² representing (Ci-4)alkyl.

The following examples are provided to illustrate the invention. These examples are illustrative only and should not be construed as limiting the invention in any way.

Experimental Part

I. Chemistry

All temperatures are stated in °C. Commercially available starting materials were used as received without further purification. Unless otherwise specified, all reactions were carried out in oven-dried glassware under an atmosphere of nitrogen. Compounds were purified by flash column chromatography on silica gel or by preparative HPLC. Compounds described in the invention are characterised by LC-MS data (retention time tR is given in min; molecular weight obtained from the mass spectrum is given in g/mol) using the conditions listed below. In cases where compounds of the present invention appear as a mixture of conformational isomers, particularly visible in their LC- MS spectra, the retention time of the most abundant conformer is given. In some cases compounds are isolated after purification in form of the corresponding ammonium salt ( ), such compounds are marked accordingly.

Analytical LC-MS equipment:

HPLC pump: Binary gradient pump, Agilent G4220A or equivalent

Autosampler: Gilson LH215 (with Gilson 845z injector) or equivalent

Column compartment: Dionex TCC-3000RS or equivalent

Degasser: Dionex SRD-3200 or equivalent Make-up pump: Dionex HPG-3200SD or equivalent

DAD detector: Agilent G4212A or equivalent

MS detector: Single quadrupole mass analyzer, Thermo Finnigan MSQPIus or equivalent

ELS detector: Sedere SEDEX 90 or equivalent

LC-MS with acidic conditions

Method A: Column: Zorbax SB-aq (3.5 μιτι, 4.6 x 50 mm). Conditions: MeCN [eluent A]; water + 0.04% TFA [eluent B]. Gradient: 95% B→ 5% B over 1.5 min (flow: 4.5 mL/min). Detection: UV/Vis + MS.

Method B: Column: Zorbax RRHD SB-aq (1.8 μιη, 2.1 x 50 mm). Conditions: MeCN [eluent A]; water + 0.04% TFA [eluent B]. Gradient: 95% B→ 5% B over 2.0 min (flow: 0.8 mL/min). Detection: UV/Vis + MS.

Method C: Waters Acquity Binary, Solvent Manager, MS: Waters SQ Detector, DAD: Acquity UPLC PDA Detector, ELSD: Acquity UPLC ELSD. Column ACQU ITY UPLC CSH C18 1.7um 2.1x50 mm from Waters, thermostated in the Acquity UPLC Column Manager at 60°C. Eluents: A: H20 + 0.05% formic acid; B: MeCN + 0.045% formic acid. Method: Gradient: 2% B 98% B over 2.0 min. Flow: 1.0 mL/min. Detection: UV 214nm and ELSD, and MS, tR is given in min.

LC-MS with basic conditions

Method D: Column: Waters BEH Cie (3.0 x 50mm, 2.5μιτι). Eluents: A: Water/NH3 [c(NH ₃ ) = 13 mmol/l], B: MeCN, Method: 5%B to 95%B in 2min, Flow 1.6ml/min, Detection UV: 214nm.

Preparative HPLC equipment:

Gilson 333/334 HPLC pump equipped with Gilson LH215, Dionex SRD-3200 degasser,

Dionex ISO-3100A make-up pump, Dionex DAD-3000 DAD detector, Single quadrupole mass analyzer MS detector, Thermo Finnigan MSQ Plus, MRA100-000 flow splitter, Polymer Laboratories PL-ELS1000 ELS detector.

Preparative HPLC with basic conditions

Column: Waters XBridge (10 μιτι, 75 x 30 mm). Conditions: MeCN [eluent A]; water + 0.5% NH ₄ OH (25% aq.) [eluent B]; Gradient see Table 1 (flow: 75 mL/min), the starting percentage of Eluent A (x) is determined depending on the polarity of the compound to purify. Detection: UV/Vis + MS.

Table 1

Preparative HPLC with acidic conditions Column: Waters Atlantis T3 (10 μιτι, 75 x 30 mm). Conditions: MeCN [eluent A]; water + 0.5% HC0 ₂ H [eluent B]; Gradient see Table 2 (flow: 75 mL/min), the starting percentage of Eluent A (x) is determined depending on the polarity of the compound to purify. Detection: UV/Vis + MS.

Table 2

Abbreviations (as used hereinbefore or hereinafter):

AcOH acetic acid

anh. anhydrous

aq. aqueous

atm atmosphere

Boc tert-butyloxycarbonyl

BOP (benzotriazol-1 -yloxy)-tris(dimethylamino)-phosphonium hexafluorophosphate d days

DCM dichloromethane

DIPEA diisopropyl-ethylamine, Hunig's base

DMAP 4-Dimethylaminopyridine

DMF dimethylformamide

DMSO dimethylsulfoxide

dppf 1 ,1 '-bis(diphenylphosphino)ferrocene

Et ethyl

Et ₂ 0 diethylether

EtOAc ethyl acetate

EtOH ethanol

Ex. example

FC flash chromatography on silica gel

h hour(s)

HATU (1 -[Bis(dimethylamino)methylene]-1 H-1 ,2,3-triazolo[4,5-b]pyridinium 3-oxid

hexafluorophosphate

hept heptane(s)

HCI hydrochloric acid or hydrogen chloride

HPLC high performance liquid chromatography HV high vacuum conditions

<Bu isobutyl

Pr isopropyl

LC-MS liquid chromatography - mass spectrometry

Lit. Literature

M mol/l

Me methyl

MeCN acetonitrile

MeOH methanol

MgS0 ₄ magnesium sulfate

mL milliliter

min minute(s)

microwave

NaHC0 ₃ sodium hydrogencarbonate

NaOH sodium hydroxide

NMP N-methyl-2-pyrrolidone

"Pr n-propyl

OAc acetate

Pd ₂ dba ₃ Tris(dibenzylideneacetone)dipalladium(0)

Pd(dppf)CI ₂ [1 ,1'-bis(diphenylphosphino)-ferrocene]dichloropalladium (II)

Pd(dppf)CI ₂ -DCM [1 ,1 '-bis(diphenylphosphino)-ferrocene]dichloropalladium (II) complex with dichloromethane

Pd(OAc) ₂ palladium(ll) acetate

Ph phenyl

PPh ₃ triphenyl phosphine

prep. Preparative

PyBOP (benzotriazol-l-yl-oxy)-tripyrrolidino-phosphonium hexafluorophosphate rac racemic

RM reaction mixture

RT room temperature

RuPhos 2-dicyclohexylphosphino-2',6'-diisopropoxybiphenyl

s second(s)

sat. saturated (if not indicated otherwise: sat. aq.)

tBu tert-butyl = tertiary butyl

TEA triethylamine

TFA trifluoroacetic acid THF tetrahydrofuran

TLC thin layer chromatography

tosyl p-toluene-sulfonyl

t _R retention time

triflate trifluoromethanesulfonate

A- Preparation of precursors and intermediates for benzothiophene derivatives

A.1. Synthesis of pyrimidine halide derivatives of formula (A3) [X = S]

A.1.1. 6-Chloro-N-(2-(2,7-dimethylbenzo[b]thiophen-3-yl)ethyl)pyrim idin-4-amine

To a solution of 2-(2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine (4.32 g, 21.03 mmol) in 2-propanol (100 mL) at RT are added TEA (10.3 mL, 73.89 mmol) and 4,6-dichloropyrimidine (3.84 g, 25.26 mmol). The RM is refluxed (90°C), under nitrogen, for 1.5h and is then allowed to cool to RT. DCM (150 mL) and water (75 mL) are added and the layers are separated. The aq. layer is extracted twice with DCM and the combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (DCM) affords 6-chloro-N-(2-(2,7-dimethylbenzo[b]thiophen-3-yl)ethyl)pyrim idin-4-amine as a beige solid (4.30 g, 64%). LC-MS A: t _R = 0.96 min; [M+H] ⁺ = 318.03 .

A.1.1.1. 2-(2,7-Ddimethylbenzo[b]thiophen-3-yl)ethan-1-amine

To a solution of 2,7-dimethylbenzo[b]thiophene-3-carbaldehyde (5.84 g, 30.69 mmol) in nitromethane (85 mL) are added successively molecular sieves (4 angstrom, 0.90 g), butylamine (0.362 mL, 3.62 mmol) and acetic acid (0.359 mL, 6.26 mmol). The RM is heated to 95°C, under nitrogen, for 2h. The RM is then filtered and the filtrate is concentrated to dryness under reduced pressure. Purification by FC (heptane/DCM = 4/1 ) affords 2,7-dimethyl-3-(2-nitrovinyl)benzo[b]thiophene as a yellow solid (5.09 g, 71 %). LC-MS A: t _R = 0.97 min; no ionisation.

To a cooled (0°C) solution of lithium aluminum hydride (2 M in THF, 37 mL, 74 mmol) in anh. THF (80 mL) is added dropwise a solution of 2,7-dimethyl-3-(2-nitro-vinyl)benzo[b]thiophene (4.94 g, 21.17 mmol) in anh. THF (60 mL). The mixture is then heated at reflux (80°C), under nitrogen, for 2.5h. The cooled (0°C) RM is treated successively with water (2.8 mL), 15% aq. NaOH (2.8 mL), and water (8.5 mL). The resulting heterogeneous mixture is then filtered and the separated solid is washed with Et20. The layers of the filtrate are separated and the aqueous layer is extracted with Et20. The combined organic layers are then dried over anh. MgSCX filtered and concentrated to dryness under reduced pressure affording 2-(2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1-amine as an orange oil (4.32 g, 99%). LC-MS A: t _R = 0.62 min; [M+H] ⁺ = 206.1 1 .

A.1.1.2. 2,7-Dimethylbenzo[b]thiophene-3-carbaldehyde

To a cooled (0°C) solution of 2,7-dimethylbenzo[b]thiophene (2.65 g, 16.33 mmol) in anh. DCM (40 mL) is added dropwise tin(IV) chloride (3.83 mL, 32.72 mmol) and the mixture is further stirred at 0°C, under nitrogen, for 15 min. Dichloromethyl methyl ether (1.81 mL, 19.61 mmol) is then added and the mixture is allowed to stir at RT, under nitrogen, for 1 h. The resulting RM is then poured onto ice-water (100 mL) and 1 M aq. HCI (75 mL) is added. The layers are separated and the aq. layer is extracted twice with DCM. The combined organic layers are dried over anh. MgS0 ₄ , filtered and concentrated to dryness under reduced pressure. Purification by FC (heptane/DCM = 7/3) affords 2,7-dimethylbenzo[b]thiophene-3- carbaldehyde as a yellow solid (2.96 g, 95%). LC-MS A: t _R = 0.89 min; no ionization.

A.1.1.3. 2,7-Dimethylbenzo[b]thiophene

To a solution of 2-methylbenzenethiol (8.00 mL, 66.52 mmol) in anh. acetone (70 mL) are added successively potassium carbonate (1 1.95 g, 86.46 mmol) and 2,3-dichloroprop-1 -ene (6.13 mL, 66.50 mmol). The RM is heated at reflux (60°C), under nitrogen, for 1 h. The RM is then allowed to cool to RT and is concentrated to dryness under reduced pressure. EtOAc (100 mL) and water (100 mL) are added and the layers are separated. The aq. layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure giving (2- chloroallyl)(o-tolyl)sulfane as a dark yellow oil (13.22 g, 100%). LC-MS A: t _R = 0.95 min; no ionization.

A solution of (2-chloroallyl)(o-tolyl)sulfane (13.22 g, 66.52 mmol) in N,N-diethylaniline (150 mL) is heated to 185°C, under nitrogen, for 45h. The resulting RM is then allowed to cool to RT, diluted with EtOAc (300 mL) and washed with 1 M aq. HCI (4 x 200 mL). The organic layer is then dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (heptane/DCM = 19/1 ) affords 2,7-dimethylbenzo[b]thiophene as a yellow oil (7.97 g, 74%). LC-MS A: t _R = 0.93 min; no ionization.

A.1.2. N-(2-(Benzo[b]thiophen-3-yl)ethyl)-6-chloropyrimidin-4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(benzo[b]thiophen- 3-yl)ethan-1 -amine. LC-MS A: t _R = 0.90 min; [M+H] ⁺ = 289.94 .

A.1.2.1. 2-(Benzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using benzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.54 min; [M+H] ⁺ = 178.30 .

A.1.3. 6-Chloro-N-(2-(2-methylbenzo[b]thiophen-3-yl)ethyl)pyrimidin -4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(2- methylbenzo[b]thiophen-3-yl)ethan-1-amine. LC-MS A: t _R = 0.93 min; [M+H] ⁺ = 304.03 .

A.1.3.1. 2-(2-Methylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 2- methylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.57 min; [M+H] ⁺ = 192.29 .

A.1.4. 6-Chloro-N-(2-(5-fluoro-2J-dimethylbenzo[b]thiophen-3-yl)eth yl)pyrimidin -amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(5-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 336.23 . A.1.4.1. 2-(5-Fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 5-fluoro-2,7- dimethylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.65 min; [M+H] ⁺ = 224.26 .

A.1.4.2. 5-Fluoro-2,7-dimethylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 5-fluoro-2,7- dimethylbenzo[b]thiophene. LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 209.24 .

A.1.4.3. 5-Fluoro-2,7-dimethylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 4-fluoro-2- methylbenzenethiol. LC-MS A: t _R = 0.96 min; no ionization.

A.1.5. 6-Chloro-N-(2-(4-fluoro-2J-dimethylbenzo[b]thiophen-3-yl)eth yl)pyrimidin -amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(4-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.99 min; [M+H] ⁺ = 336.1 1 .

A.1.5.1. 2-(4-Fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 4-fluoro-2,7- dimethylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.64 min; [M+H] ⁺ = 224.09 .

A.1.5.2. 4-Fluoro-2,7-dimethylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 4-fluoro-2,7- dimethylbenzo[b]thiophene. LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 209.05 .

A.1.5.3. 4-Fluoro-2,7-dimethylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 5-fluoro-2- methylbenzenethiol. LC-MS D: t _R = 1.28 min; no ionization.

A.1.6. 6-Chloro-N-(2-(4^hloro-2J-dimethylbenzo[b]thiophen-3-yl)ethy l)pyrimidin -amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(4-chloro-2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 1.02 min; [M+H] ⁺ = 352.04 .

A.1.6.1. 2-(4-Chloro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 4-chloro- 2,7-dimethylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.65 min; [M+H] ⁺ = 240.16 .

A.1.6.2. 4-Chloro-2,7-dimethylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 4-chloro- 2,7-dimethylbenzo[b]thiophene. LC-MS A: t _R = 0.97 min; [M+H] ⁺ = 224.48 .

A.1.6.3. 4-Chloro-2,7-dimethylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 5-chloro-2- methylbenzenethiol. LC-MS D: t _R = 1.36 min; no ionization. A.1.7. 6-Chloro-N-(2-(6-fluoro-2 -dimethylbenzo[b]thiophen-3-yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(6-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 336.55 .

A.1.7.1. 2-(6-Fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 6-fluoro-2,7- dimethylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.64 min; [M+H] ⁺ = 224.48 .

A.1.7.2. 6-Fluoro-2,7-dimethylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 6-fluoro-2,7- dimethylbenzo[b]thiophene. LC-MS A: t _R = 0.92 min; no ionization.

A.1.7.3. 6-Fluoro-2,7-dimethylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 3-fluoro-2- methylbenzenethiol. LC-MS A: t _R = 0.96 min; [M+H] ⁺ = 181.27 .

A.1.8. 6-Chloro-N-(2-(4-fluoro -methoxy-2-methylbenzo[b]thiophen -yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(4-fluoro-7-methoxy- 2-methylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.96 min; [M+H] ⁺ = 352.06 .

A.1.8.1. 2-(4-Fluoro-7-methoxy-2-methylbenzo[b]thiophen-3-yl)ethan-1- amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 4-fluoro-7- methoxy-2-methylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.61 min; [M+H] ⁺ = 240.1 1 .

A.1.8.2. 4-Fluoro-7-methoxy-2-methylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 4-fluoro-7- methoxy-2-methylbenzo[b]thiophene. LC-MS A: t _R = 0.91 min; [M+H] ⁺ = 225.11 .

A.1.8.3. 4-Fluoro-7-methoxy-2-methylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 5-fluoro-2- methoxybenzenethiol. LC-MS A: t _R = 0.94 min; no ionization.

A.1.9. 6-Chloro-N-(2-(4-chloro-7-methoxy-2-methylbenzo[b]thiophen-3 -yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(4-chloro-7-methoxy- 2-methylbenzo[b]thiophen-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.99 min; [M+H] ⁺ = 368.07 .

A.1.9.1. 2-(4-Chloro-7-methoxy-2-methyl benzo[b]thiophen-3-yl)ethan-1 -amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 4-chloro-7- methoxy-2-methylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.63 min; [M+H] ⁺ = 256.1 1 .

A.1.9.2. 4-Chloro-7-methoxy-2-methylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 4-chloro-7- methoxy-2-methylbenzo[b]thiophene. LC-MS A: t _R = 0.94 min; [M+H] ⁺ = 241.09 . A.1.9.3. 4-Chloro-7-methoxy-2-methylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 5-chloro-2- methoxybenzenethiol. LC-MS A: t _R = 0.97 min; no ionization.

A.1.10. 6-Chloro-N-(2-(7 hloro-5-fluoro-2-methylbenzo[b]thiophen -yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(7-chloro-5-fluoro-2- methylbenzo[b]thiophen-3-yl)ethan-1-amine. LC-MS A: t _R = 1.00 min; [M+H] ⁺ = 356.05 .

A.1.10.1. 2-(7-Chloro-5-fluoro-2-methylbenzo[b]thiophen-3-yl)ethan-1-a mine

The title compound is prepared according to the procedure described above in A.1.1.1. using 7-chloro-5- fluoro-2-methylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: tR = 0.67 min; no ionization.

A.1.10.2. 7-Chloro-5-fluoro-2-methylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 7-chloro-5- fluoro-2-methylbenzo[b]thiophene. LC-MS A: tR = 0.94 min; no ionization.

A.1.10.3. 7-Chloro-5-fluoro-2-methylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 2-chloro-4- fluorobenzenethiol. LC-MS A: tR = 0.97 min; no ionization.

A.1.11. 6-Chloro-N-(2-(4 -dichloro-2-methylbenzo[b]thiophen-3-yl)ethyl)pyrimidin-4-am ine

The title compound is prepared according to the procedure described above in A.1.1. using 2-(4,7-dichloro-2- methylbenzo[b]thiophen-3-yl)ethan-1-amine. LC-MS A: t _R = 1.03 min; [M+H] ⁺ = 372.00 .

A.1.11.1. 2-(4,7-Dichloro-2-methylbenzo[b]thiophen-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in A.1.1.1. using 4,7-dichloro-

2-methylbenzo[b]thiophene-3-carbaldehyde. LC-MS A: t _R = 0.68 min; [M+H] ⁺ = 260.07 .

A.1.11.2. 4,7-Dichloro-2-methylbenzo[b]thiophene-3-carbaldehyde

The title compound is prepared according to the procedure described above in A.1.1.2. using 4,7-dichloro- 2-methylbenzo[b]thiophene. LC-MS A: tR = 0.98 min; no ionization.

A.1.11.3. 4,7-Dichloro-2-methylbenzo[b]thiophene

The title compound is prepared according to the procedure described above in A.1.1.3. using 2,5- dichlorobenzenethiol. LC-MS A: tR = 1.01 min; no ionization.

A.1.12. 3-(2-((6-Chloropyrimidin -yl)amino)ethyl)-7-methoxybenzo[b]thiophene-2-carbonitrile

To a solution of 3-(2-aminoethyl)-7-methoxybenzo[b]thiophene-2-carbonitrile hydrochloride (485 mg, 1.79 mmol) in 2-propanol (20 mL) at RT are added TEA (0.87 mL, 6.25 mmol) and 4,6-dichloropyrimidine (319 mg, 2.14 mmol). The RM is refluxed (90°C), under nitrogen, for 15h and is then allowed to cool to RT. DCM and water are added and the layers are separated. The aq. layer is extracted twice with DCM and the combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords 3-(2-((6-chloropyrimidin-4-yl)amino)ethyl)-7- methoxybenzo[b]thiophene-2-carbonitrile as a colorless solid (254 mg, 41 %). LC-MS B: t _R = 1.00 min; [M+H] ⁺ = 345.05 .

A.1.12.1. 3-(2-Aminoethyl)-7-methoxybenzo[b]thiophene-2-carbonitrile hydrochloride

To a solution of tert-butyl (2-(2-cyano-7-methoxybenzo[b]thiophen-3-yl)ethyl)carbamate (672 mg, 1.88 mmol) in DCM (20 mL) is added 4 M HCI in dioxane (4.65 mL, 18.60 mmol) and the RM is stirred at RT for 4h. The RM is then concentrated to dryness under reduced pressure affording 3-(2-aminoethyl)-7- methoxybenzo[b]thiophene-2-carbonitrile hydrochloride as a pale green solid (485 mg, 96%). LC-MS B: tR = 0.61 min; [M+H] ⁺ = 233.1 1 .

A.1.12.2. Tert-butyl (2-(2-cyano-7-methoxybenzo[b]thiophen-3-yl)ethyl)carbamate

A mixture of 3-bromo-7-methoxybenzo[b]thiophene-2-carbonitrile (1.500 g, 5.15 mmol), potassium (2- ((tert-butoxycarbonyl)amino)ethyl)trifluoroborate (1.496 g, 5.66 mmol) and cesium carbonate (5.031 g, 15.40 mmol) in toluene (40 mL) and water (13 mL) is degassed three times. Palladium(ll) acetate (57.8 mg, 0.25 mmol) and RuPhos (253 mg, 0.51 mmol) are then added and the mixture is heated to 95°C, under nitrogen, overnight. The RM is allowed to cool to RT. Water is added and the RM is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords tert-butyl (2-(2-cyano-7-methoxybenzo[b]thiophen-3-yl)ethyl)carbamate as an orange solid (672 mg, 39%). LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 333.11 .

A.1.12.3. 3-Bromo-7-methoxybenzo[b]thiophene-2-carbonitrile

To a cooled (0°C) solution of 3-bromo-7-methoxybenzo[b]thiophene-2-carboxamide (5.28 g, 14.20 mmol) in anh. DMF (70 mL) is added portionwise cyanuric chloride (3.97 g, 21.30 mmol) and the RM is stirred at 0°C, under nitrogen, for 1.5h. Water is added and the RM is extracted three times with Et20. The combined organic layers are washed successively with water and brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords 3-bromo-7-methoxybenzo[b]thiophene-2-carbonitrile as a beige solid (3.412 g, 90%). LC-MS B: tR = 1.05 min; no ionization.

A.1.12.4. 3-Bromo-7-methoxybenzo[b]thiophene-2-carboxamide

To a cooled (0°C) solution of 3-bromo-7-methoxybenzo[b]thiophene-2-carboxylic acid (5.873 g, 15.90 mmol) and anh. DMF (a few drops) in anh. DCM (80 mL) is added dropwise oxalyl chloride (1.88 mL, 21.80 mmol). The mixture is stirred at 0°C, under nitrogen, for 10 min and then at RT for 2h. The RM is then cooled to 0°C, treated dropwise with a solution of ammonium hydroxide (25% NH ₃ in H20, 18.8 mL, 252 mmol), and stirred at RT for 2h. DCM is then removed under reduced pressure, 10% aq. NaOH is added to the aqueous residue, and the RM is extracted three times with EtOAc. The combined organic layers are washed successively with water and brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording 3-bromo-7-methoxybenzo[b]thiophene-2-carboxamide as a brown solid (5.28 g, quantitative). LC-MS B: t _R = 0.83 min; [M+H] ⁺ = 285.99 .

A.1.12.5. 3-Bromo-7-methoxybenzo[b]thiophene-2-carboxylic acid

To a solution of methyl 3-bromo-7-methoxybenzo[b]thiophene-2-carboxylate (6.151 g, 15.90 mmol) in MeOH (40 mL) and THF (40 mL) is added 1 M aq. NaOH (40.0 mL, 40.0 mmol) and the RM is stirred at

RT for 2.5h. The organic solvents are then removed under reduced pressure. Water (50 mL) is added and the mixture is extracted three times with EtOAc. The aqueous layer is then acidified with 1 M aq. HCI and extracted three times with EtOAc. The combined organic extracts are washed successively with water and brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording 3- bromo-7-methoxybenzo[b]thiophene-2-carboxylic acid as a brown solid (5.873 g, quantitative). LC-MS B: t _R = 0.88 min; [M+H] ⁺ = 286.91 .

A.1.12.6. Methyl 3-bromo-7-methoxybenzo[b]thiophene-2-carboxylate

To a cooled (0°C) mixture of tert-butyl nitrite (3.90 mL, 29.50 mmol) and copper(ll) bromide (7.295 g, 32.30 mmol) in anh. MeCN (80 mL) is added portionwise methyl 3-amino-7-methoxybenzo[b]thiophene-2- carboxylate (5.000 g, 20.90 mmol). The RM is stirred at 0°C for 30 min, and then at RT for 30 min. 1 M aq. HCI (50 mL) is then added and the mixture is extracted three times with EtOAc. The combined organic layers are dried over anh. MgS04, filtered and concentrated to dryness under reduced pressure affording methyl 3-bromo-7-methoxybenzo[b]thiophene-2-carboxylate as an orange solid (6.150 g, 98%). LC-MS B: t _R = 1.05 min; [M+H] ⁺ = 300.97 .

A.1.12.7. Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

To a mixture of 2-fluoro-3-methoxybenzonitrile (7.000 g, 45.90 mmol) and potassium carbonate (12.802 g, 91.70 mmol) in DMF (50 mL) is added dropwise methyl 2-mercaptoacetate (4.53 mL, 48.10 mmol). The RM is stirred at RT, under nitrogen, for 1.5h. Water is then added, and the resulting suspension is filtered. The separated solid is then washed with water and dried under high vacuum to give methyl 3-amino-7- methoxybenzo[b]thiophene-2-carboxylate as a beige solid (10.200 g, 94%). LC-MS B: t _R = 0.90 min;

[M+H] ⁺ = 238.07 .

A.1.13. 3-(2-((6-Chloropyrimidin -yl)amino)ethyl)-5-fluoro-7-methylbenzo[b]thiophene-2-carbon itrile

To a solution of 3-(2-aminoethyl)-5-fluoro-7-methylbenzo[b]thiophene-2-carbon itrile hydrochloride (688 mg, 1.96 mmol) in 2-propanol (25 mL) at RT are added TEA (1.16 mL, 8.36 mmol) and 4,6-dichloropyrimidine (427 mg, 2.87 mmol). The RM is refluxed (90°C), under nitrogen, for 16h and is then allowed to cool to RT. DCM and water are added and the layers are separated. The aq. layer is extracted twice with DCM and the combined organic layers are then washed with brine, dried over anh. MgS04, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords 3-(2-((6-chloropyrimidin-4-yl)amino)ethyl)-5- fluoro-7-methylbenzo[b]thiophene-2-carbonitrile as an orange solid (380 mg, 46%). LC-MS B: t _R = 1.05 min; [M+H] ⁺ = 347.11 . A.1.13.1. 3-(2-Aminoethyl)-5-fluoro-7-methylbenzo[b]thiophene-2-carbon itrile hydrochloride

To a solution of tert-butyl (2-(2-cyano-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)car bamate (819 mg, 1.96 mmol) in DCM (20 mL) is added 4 M HCI in dioxane (4.90 mL, 19.60 mmol) and the RM is stirred at RT for 15h. The RM is then concentrated to dryness under reduced pressure affording 3-(2-aminoethyl)- 5-fluoro-7-methylbenzo[b]thiophene-2-carbonitrile hydrochloride as a pale green solid (688 mg, quantitative). LC-MS B: t _R = 0.63 min; [M+H] ⁺ = 234.96 .

A.1.13.2. Tert-butyl (2-(2-cyano-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)car bamate

A mixture of 3-bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carbonitrile (1.622 g, 5.58 mmol), potassium (2-((tert-butoxycarbonyl)amino)ethyl)trifluoroborate (1.624 g, 6.14 mmol) and cesium carbonate (5.458 g, 16.80 mmol) in toluene (40 mL) and water (13 mL) is degassed three times. Palladium(ll) acetate (62.7 mg, 0.27 mmol) and RuPhos (274 mg, 0.55 mmol) are then added and the mixture is heated to 95°C, under nitrogen, for 15h. The RM is allowed to cool to RT. Water is added and the RM is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords tert-butyl (2-(2-cyano-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)car bamate as a yellow solid (818 mg, 44%). LC-MS B: t _R = 1.08 min; [M+H] ⁺ = 335.12 .

A.1.13.3. 3-Bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carbonitrile

To a cooled (0°C) solution of 3-bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxamide (4.508 g, 12.50 mmol) in anh. DMF (60 mL) is added portionwise cyanuric chloride (3.759 g, 20.20 mmol) and the RM is stirred at 0°C, under nitrogen, for 2h. Water is added and the RM is extracted three times with Et ₂ 0. The combined organic layers are washed successively with water and brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords 3-bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carbonitrile as a colorless solid (3.244 g, 89%). LC-MS B: t _R = 1.07 min; no ionization.

A.1.13.4. 3-Bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxamide

To a cooled (0°C) solution of 3-bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxylic acid (4.240 g, 12.50 mmol) and anh. DMF (a few drops) in anh. DCM (60 mL) is added dropwise oxalyl chloride (1.40 mL, 16.20 mmol). The mixture is stirred at 0°C, under nitrogen, for 10 min and then at RT for 1.5h. The RM is then cooled to 0°C, treated dropwise with a solution of ammonium hydroxide (25% N H3 in H20, 14 mL, 187 mmol), and stirred at RT for 2h. DCM is then removed under reduced pressure, water is added, and the resulting suspension is filtered. The isolated solid is further dried under high vacuum affording 3- bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxamide as a colorless solid (4.508 g, quantitative). LC- MS B: tR = 0.88 min; [M+H] ⁺ = 287.98 . A.1.13.5. 3-Bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxylic acid

To a solution of methyl 3-bromo-5-fluoro-7-methylbenzo[b]thiophene-2-carboxylate (5.093 g, 15.10 mmol) in MeOH (40 mL) and THF (40 mL) is added 1 M aq. NaOH (38.0 mL, 38.0 mmol) and the RM is stirred at RT for 1 h. The organic solvents are then removed under reduced pressure, water is added to the residue, and the mixture is acidified with 2 M aq. HCI. EtOAc is then added and the resulting suspension is filtered. The isolated solid is further dried under high vacuum affording 3-bromo-5-fluoro-7- methylbenzo[b]thiophene-2-carboxylic acid as a colorless solid (4.240 g, 97%). LC-MS B: tR = 0.94 min; no ionization.

A.1.13.6. Methyl 3-bromo-5-f luoro-7-methyl benzo[b]thiophene-2-carboxy late

To a cooled (0°C) mixture of tert-butyl nitrite (4.35 mL, 32.90 mmol) and copper(ll) bromide (8.145 g, 36.10 mmol) in anh. MeCN (120 mL) is added portionwise methyl 3-amino-5-fluoro-7-methylbenzo[b]thiophene- 2-carboxylate (5.629 g, 23.30 mmol). The RM is stirred at 0°C for 15 min, and then at RT for 30 min. 1 M aq. HCI (50 mL) is then added and the mixture is extracted three times with EtOAc. The combined organic layers are dried over anh. MgSCX filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords methyl 3-bromo-5-fluoro-7- methylbenzo[b]thiophene-2-carboxylate as a light yellow solid (5.093 g, 72%). LC-MS B: t _R = 1.10 min; no ionization.

A.1.13.7. Methyl 3-amino-5-fluoro-7-methylbenzo[b]thiophene-2-carboxylate

To a cooled (0°C) mixture of 2,5-difluoro-3-methylbenzonitrile (5.000 g, 32.00 mmol) and potassium carbonate (8.934 g, 64.00 mmol) in DMF (30 mL) is added dropwise a solution of methyl 2- mercaptoacetate (3.01 mL, 32.00 mmol) in DMF (5 mL). The RM is stirred at 0°C, under nitrogen, for 3.5h and then at RT for 1.5h. Water is added and the resulting suspension is filtered. The separated solid is then washed with water, dissolved in EtOAc and the resulting solution is dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords methyl 3-amino-5-fluoro-7-methylbenzo[b]thiophene-2-carboxylate as a pale yellow solid

(4.914 g, 64%). LC-MS B: t _R = 0.97 min; [M+H] ⁺ = 240.06 .

A.1.14. Ethyl 4-(6-chloropyrimidin-4-yl)-2-ethoxybenzoate

To a solution of 4,6-dichloropyrimidine (1.00 g, 6.71 mmol) in EtOH (100 mL) is added ethyl 2-ethoxy-4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate (2.149 g, 6.71 mmol) and 2 M aq. Na ₂ C0 ₃ (10.1 mL, 20.2 mmol). The mixture is then degassed with nitrogen and Pd(PP i3)4 (388 mg, 0.33 mmol) is added. The RM is then heated to 90°C, under nitrogen, for 1.5h. The RM is allowed to cool to RT, diluted with DCM and water is added. The layers are separated and the aqueous layer is extracted twice with DCM. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH = 50/1 ) affords ethyl 4-(6-chloropyrimidin-4-yl)-2-ethoxybenzoate as a colorless solid (720 mg, 35%). LC-MS A: t _R = 0.93 min; [M+H] ⁺ = 307.01 . A.1.14.1. Ethyl 2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

To a solution of ethyl 4-bromo-2-ethoxybenzoate (1.79 g, 6.55 mmol) in anh. DMF (35 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (2.496 g, 9.83 mmol), potassium acetate (1.930 g, 19.70 mmol) and [1 ,1 '-bis(diphenylphosphino)ferrocene]dichloropalladium(ll) (384 mg, 0.52 mmol). The RM is heated to 90°C, under nitrogen, for 17h. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EbO. The filtrate is washed with water and the aqueous layer is extracted twice with EbO. The combined organic layers are then washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure. Purification by FC (from DCM to DCM/MeOH = 50/1 ) affords ethyl 2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)benzoate as a yellow oil (1.85 g, 88%). LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 321.13 .

A.1.14.2. Ethyl 4-bromo-2-ethoxybenzoate

To a solution of 4-bromo-2-hydroxybenzoic acid (2.00 g, 9.22 mmol) in anh. DMF (15 mL) at RT are added potassium carbonate (2.547 g, 18.40 mmol) and iodoethane (1.48 mL, 18.40 mmol) and the RM is heated to 80°C for 16h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane/DCM = 3/7 to DCM) affords ethyl 4-bromo-2-ethoxybenzoate as a yellow solid (1.79 g, 71 %). LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 273.07 .

A.1.15. 3-(2-((6-chloropyrimidin-4-yl)amino)ethyl)benzo[b]thiophene- 2-carbonitrile

To a solution of 3-(2-aminoethyl)benzo[b]thiophene-2-carbonitrile hydrochloride (1480 mg, 6.12 mmol) in 2- propanol (30 mL) at RT under N ₂ is added 4,6-dichloropyrimidine (1094 mg, 7.34 mmol) and TEA (2.98 mL, 21.4 mmol). The RM is heated at 90°C overnight, then cooled to RT, DCM and water are added, the phases are separated and the aqueous layer is extracted twice with DCM. Organic layers are combined and washed with brine, dried over a phase separator and concentrated under reduced pressure. The residue is purified by FC (HepLEtOAc, 100:0 to 20:80), yielding the title compound as a light orange powder (828 mg, 43%). LC-MS A: t _R = 0.96 min; [M+H] ⁺ = 315.09.

A.1.15.1. 3-(2-Aminoethyl)benzo[b]thiophene-2-carbonitrile hydrochloride

Following the procedure described in A.1.12.1., using tert-butyl (2-(2-cyanobenzo[b]thiophen-3- yl)ethyl)carbamate, the title compound is obtained as a yellow powder. LC-MS A: t _R = 0.582 min; [M+H] ⁺ = 203.21.

A.1.15.2. 3-(2-Aminoethyl)benzo[b]thiophene-2-carbonitrile hydrochloride

Following the procedure described in A.1.12.2., using 3-bromobenzo[b]thiophene-2-carbonitrile and potassium tert-butyl N-[2-(trifluoroboranuidyl)ethyl]carbamate, the title compound is obtained as a yellow powder. LC-MS A: t _R = 1.01 min; no ionization. ¹ H NMR (400 MHz, d6-DMSO) δ: 8.09 (dd, J1 = 8.0 Hz, J2 = 33.7 Hz, 2 H), 7.58-7.65 (m, 2 H), 7.02 (t, J = 5.7 Hz, 1 H), 3.15-3.27 (m, 4 H), 1.32 (s, 9 H). A.2. Synthesis of substituted 2-(benzo[b]thiophen-3-yl)ethan-1-amine derivatives of formula (A1) [X = S]

A.2.1. 2-(2-Bromo-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethan-1-am ine

To a suspension of 2-(2-(2-bromo-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)i soindoline-1 ,3-dione (335 mg, 0.80 mmol) in MeOH (5 mL) at RT is added hydrazine hydrate (50-60% hydrazine, 0.39 mL) and the mixture is heated to 50°C, under nitrogen, for 2h. The RM is allowed to cool to RT and a precipitate corresponding to 2,3- dihydrophthalazine-1 ,4-dione is separated by filtration. The filtrate is concentrated to dryness under reduced pressure and the obtained solid is triturated in DCM. The heterogeneous mixture is then filtered and the filtrate is concentrated to dryness under reduced pressure affording 2-(2-bromo-5-fluoro-7-methylbenzo[b]thiophen-3- yl)ethan-1 -amine as a yellow solid (200 mg, 87%). LC-MS A: t _R = 0.66 min; [M+H] ⁺ = 288.00 .

A.2.1.1. 2-(2-(2-Bromo-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)i soindoline-1 ,3-dione

To a solution of 2-(2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoli ne-1 ,3-dione (500 mg, 1.47 mmol) in DMF (4 mL) is added dropwise a solution of N-bromosuccinimide (344 mg, 1.93 mmol) in DMF (4 mL). The RM is heated to 70°C, under nitrogen, for 1.5h. A second addition of N-bromosuccinimide (131 mg, 0.73 mmol) is then performed and the mixture is further heated to 70°C for 1 h. The RM is allowed to cool to RT. Water and Et20 are then added and the obtained precipitate is filtered affording 2-(2-(2- bromo-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoli ne-1 ,3-dione as a colorless solid that is further dried under high vacuum (335 mg, 54%). LC-MS A: tR = 1.05 min; no ionization.

A.2.1.2. 2-(2-(5-Fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoli ne-1,3-dione

To a solution of 2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethan-1-ol (5.54 g, 26.34 mmol) in THF (110 mL) at RT are added successively triphenylphosphine (10.36 g, 39.49 mmol) and phthalimide (5.87 g, 39.89). A solution of diethyl azodicarboxylate (4.98 mL, 27.16 mmol) in THF (20 mL) is then added dropwise and the RM is stirred at RT, under nitrogen, for 1.5h. The RM is concentrated to dryness under reduced pressure. The obtained solid is triturated in EtOAc, filtered, and stirred in EtOH for 0.5h. A subsequent filtration affords 2-(2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoli ne-1 ,3-dione as a colorless solid that is further dried under high vacuum (7.43 g, 83%). LC-MS A: tR = 1.00 min; no ionization.

A.2.1.3. 2-(5-Fluoro-7-methylbenzo[b]thiophen-3-yl)ethan-1-ol

To a cooled (-78°C) solution of ethyl 2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)acetate (6.88 g, 27.26 mmol) in anh. toluene (80 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 81.8 mL, 81.8 mmol). The mixture is further stirred at -78°C, under nitrogen, for 5 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 15 min and the cooled RM is treated successively with water (75 mL) and with 1 N aq. NaOH (150 mL). The mixture is then allowed to warm-up to RT and the layers are separated. The aqueous layer is extracted twice with EtOAc. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (DCM) affords 2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethan-1-ol as a yellow oil (5.54 g, 97%) LC-MS A: tR = 0.80 min; no ionization.

A.2.1.4. Ethyl 2-(5-f luoro-7-methyl benzo[b]thiophen-3-y l)acetate

To a solution of 5-fluoro-7-methylbenzo[b]thiophen-3(2H)-one (9.21 g, 50.54 mmol) in anh. toluene (250 mL) is added (carbethoxymethylene)triphenylphosphorane (17.61 g, 50.54 mmol) and the RM is heated at reflux, under nitrogen, for 21 h. The RM is allowed to cool to RT and is concentrated to dryness under reduced pressure. DCM is added and the obtained precipitate is separated by filtration. The filtrate is then concentrated to dryness under reduced pressure and the residue is purified by FC (from heptane/DCM = 9/1 to DCM) affording ethyl 2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)acetate as a pale orange solid (6.88 g, 54%). LC-MS A: t _R = 0.94 min; no ionization.

A.2.1.5. 5-Fluoro-7-methylbenzo[b]thiophen-3(2H)-one

To a cooled (0°C) solution of 2-((4-fluoro-2-methylphenyl)thio)acetic acid (13.37 g, 66.77 mmol) in anh. THF (150 mL) are added dropwise oxalyl chloride (1 1.80 mL, 133.87 mmol) and anh. DMF (5 drops). The mixture is allowed to warm-up to RT and is further stirred at RT, under nitrogen, for 20 min. The RM is then concentrated to dryness under reduced pressure and the residue is dissolved in anh. DCM (50 mL).

The obtained solution is added dropwise to a cooled (0°C) suspension of aluminum chloride (13.49 g, 101.16 mmol) in anh. DCM (100 mL) and the RM is stirred overnight at RT. The cooled (0°C) RM is then treated carefully with ice and is allowed to warm-up to RT. The layers are separated and the aqueous layer is extracted twice with DCM. The combined organic layers are then washed with aq. sat. NaHCC , dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC

(from heptane/DCM = 9/1 to DCM) affords 5-fluoro-7-methylbenzo[b]thiophen-3(2H)-one as an orange- brown solid (9.21 g, 76%). LC-MS A: t _R = 0.81 min; no ionization.

A.2.1.6. 2-((4-Fluoro-2-methylphenyl)thio)acetic acid

To a solution of ethyl 2-((4-fluoro-2-methylphenyl)thio)acetate (15.25 g, 66.80 mmol) in EtOH (90 mL) is added dropwise 1 M aq. NaOH (87.0 mL, 87.0 mmol) and the resulting solution is stirred at RT for 45 min.

The cooled (0°C) RM is then acidified by addition of 1 M aq. HCI. EtOH is then removed under reduced pressure, DCM is added and the layers are separated. The aqueous layer is extracted twice with DCM and the combined organic layers are dried over anh. MgS04, filtered and concentrated to dryness under reduced pressure affording 2-((4-fluoro-2-methylphenyl)thio)acetic acid as a pale yellow solid (13.89 g, quantitative). LC-MS A: [R = 0.74 min; no ionization.

A.2.1.7. Ethyl 2-((4-fluoro-2-methylphenyl)thio)acetate

To a solution of 4-fluoro-2-methylbenzenethiol (10.00 g, 66.80 mmol) in anh. DMF (120 mL) are added successively potassium carbonate (10.15 g, 73.43 mmol), potassium iodide (0.555 g, 3.34 mmol) and ethyl bromoacetate (8.72 mL, 73.50 mmol). The RM is heated to 80°C, under nitrogen, for 1 h. The RM is allowed to cool to RT, water is then added and this mixture is extracted three times with Et ₂ 0. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording ethyl 2-((4-fluoro-2-methylphenyl)thio)acetate as a yellow oil (16.59 g, quantitative). LC-MS A: t _R = 0.90 min; no ionization.

A.2.2. 2-(2-Chloro-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethan-1-a mine

The title compound is prepared according to the procedure described above in A.2.1. using 2-(2-(2-chloro-5-fluoro- 7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoline-1 ,3-dione. LC-MS A: t _R = 0.65 min; [M+H] ⁺ = 243.97 .

A.2.2.1. 2-(2-(2-Chloro-5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl) isoindoline-1 ,3-dione

To a solution of 2-(2-(5-fluoro-7-methylbenzo[b]thiophen-3-yl)ethyl)isoindoli ne-1 ,3-dione (150 mg, 0.44 mmol; preparation described in A.2.1.2.) in DMF (1.2 mL) is added dropwise a solution of N- chlorosuccinimide (88 mg, 0.66 mmol) in DMF (1.2 mL). The RM is heated to 70°C, under nitrogen, for 1.5h. The RM is allowed to cool to RT. Water and Et20 are then added and the layers are separated. The aqueous layer is further extracted with Et20 and the combined organic layers are washed with aq. sat. NaHCC>3, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. The obtained solid is triturated in EtOH and filtered affording 2-(2-(2-chloro-5-fluoro-7-methylbenzo[b]thiophen- 3-yl)ethyl)isoindoline-1 ,3-dione as a colorless solid that is further dried under high vacuum (174 mg, quantitative). LC-MS A: t _R = 1.04 min; no ionization.

B- Preparation of precursors and intermediates for benzofuran derivatives

B.1. Synthesis of pyrimidine halide derivatives of formula (A3) [X = O]

B.1.1. 6-Chloro-N-(2-(7-chloro-2-methylbenzofuran-3-yl)ethyl)pyrimi din-4-amine

To a solution of 2-(7-chloro-2-methylbenzofuran-3-yl)ethan-1 -amine (4.90 g, 23.36 mmol) in 2-propanol (90 mL) at RT are added TEA (1 1.5 mL, 82.62 mmol) and 4,6-dichloropyrimidine (4.27 g, 28.66 mmol). The RM is refluxed (90°C), under nitrogen, for 1 h and is then allowed to cool to RT. DCM (150 mL) and water (75 mL) are added and the layers are separated. The aq. layer is extracted twice with DCM and the combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH = 50/1 ) affords 6-chloro-N-(2-(7-chloro-2-methylbenzofuran-3-yl)ethyl)pyrimi din - amine (3.57 g, 47%). LC-MS A: t _R = 0.95 min; [M+H] ⁺ = 321.94 .

B.1.1.1. 2-(7-Chloro-2-methylbenzofuran-3-yl)ethan-1-amine

To a solution of 7-chloro-2-methylbenzofuran-3-carbaldehyde (4.78 g, 24.56 mmol) in nitromethane (115 mL) are added successively molecular sieves (4 angstrom, 0.74 g), butylamine (0.290 mL, 2.92 mmol) and acetic acid (0.287 mL, 5.01 mmol). The RM is heated to 95°C, under nitrogen, for 2h. The RM is then filtered and the filtrate is concentrated to dryness under reduced pressure affording 7-chloro-2-methyl-3- (2-nitrovinyl)benzofuran as a brown solid (5.84 g) that is used in the subsequent reduction without additional purification. LC-MS A: t _R = 0.95 min; no ionization. To a cooled (0°C) solution of lithium aluminum hydride (2 M in THF, 42.4 mL, 84.8 mmol) in anh. THF (140 mL) is added dropwise a solution of 7-chloro-2-methyl-3-(2-nitrovinyl)benzofuran (5.84 g, 24.56 mmol) in anh. THF (160 mL). The mixture is then heated at reflux (80°C), under nitrogen, for 0.5h. The cooled (0°C) RM is treated successively with water (3.2 mL), 15% aq. NaOH (3.2 mL), and water (9.6 mL). The resulting heterogeneous mixture is then filtered and the separated solid is washed with Et20. The layers of the filtrate are separated and the aqueous layer is extracted with Et20. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording 2-(7-chloro-2-methylbenzofuran-3-yl)ethan-1-amine as a brown oil (4.90 g, 95%). LC-MS A: t _R = 0.59 min; [M+H] ⁺ = 210.08 .

B.1.1.2. 7-Chloro-2-methylbenzofuran-3-carbaldehyde

To a cooled (0°C) solution of 7-chloro-2-methylbenzofuran (4.42 g, 26.52 mmol) in anh. DCM (55 mL) is added dropwise tin(IV) chloride (6.22 mL, 53.14 mmol) and the mixture is further stirred at 0°C, under nitrogen, for 15 min. Dichloromethyl methyl ether (2.94 mL, 32.50 mmol) is then added and the mixture is allowed to stir at RT, under nitrogen, for 1.5h. The resulting RM is then poured onto ice-water (200 mL) and 1 M aq. HCI (75 mL) is added. The layers are separated and the aq. layer is extracted twice with DCM. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane/DCM = 9/1 to heptane/DCM = 1/1 ) affords 7-chloro- 2-methylbenzofuran-3-carbaldehyde as a yellow solid (4.78 g, 93%). LC-MS A: tR = 0.86 min; no ionization.

B.1.1.3. 7-Chloro-2-methylbenzofuran

To a solution of 3-chloro-2-hydroxybenzaldehyde (5.00 g, 31.93 mmol) in anh. DMF (30 mL) at RT are added successively ethyl 2-bromopropanoate (4.52 mL, 34.80 mmol), potassium carbonate (4.58 g, 33.13 mmol) and potassium iodide (262 mg, 1.57 mmol). The RM is heated to 80°C, under nitrogen, for 40 min. The RM is then allowed to cool to RT. Water (100 mL) and Et20 (150 mL) are added and the layers are separated. The aq. layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure giving ethyl 2-(2-chloro-6-formylphenoxy)propanoate as a light brown oil (8.20 g, quantitative). LC-MS A: tR = 0.88 min; [M+H] ⁺ = 256.99 .

To a solution of ethyl 2-(2-chloro-6-formylphenoxy)propanoate (8.20 g, 31.93 mmol) in MeOH (120 mL) and water (30 mL) at RT is added 1 M aq. NaOH (36 mL, 36 mmol) and the RM is heated to 50°C, under nitrogen, for 1 h. The RM is then allowed to cool to RT and is treated with 1 M aq. HCI (36 mL). MeOH is removed under reduced pressure and the residual aqueous mixture is extracted twice with DCM. The combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated to dryness under reduced pressure affording 2-(2-chloro-6-formylphenoxy)propanoic acid as a light yellow solid (7.30 g, quantitative). LC-MS A: t _R = 0.72 min; [M+H] ⁺ = 228.93 . A mixture of 2-(2-chloro-6-formylphenoxy)propanoic acid (7.30 g, 31.93 mmol) in acetic anhydride (39 mL, 412 mmol) at RT is treated with sodium acetate (8.14 g, 99.23 mmol) and is then heated at reflux (150°C), under nitrogen, for 14h. The RM is allowed to cool to RT, diluted with toluene (50 mL) and treated with 1 M aq. NaOH (40 mL). After stirring at RT for 30 min, the RM is diluted with water and extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (heptane) affords 7-chloro-2- methylbenzofuran as a yellow oil (4.43 g, 83%). LC-MS A: tR = 0.90 min; no ionization.

B.1.2. 6-Chloro-N-(2-(2-methylbenzofuran-3-yl)ethyl)pyrimidin-4-ami ne

The title compound is prepared according to the procedure described above in B.1.1. using 2-(2-methylbenzofuran- 3-yl)ethan-1 -amine. LC-MS A: t _R = 0.90 min; [M+H] ⁺ = 288.06 .

B.1.2.1. 2-(2-Methy I benzofuran-3-y l)ethan-1 -amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 2- methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.54 min; [M+H] ⁺ = 176.27 .

B.1.3. 6-Chloro-N-(2-(5-fluoro-2J-dimethylbenzofuran-3-yl)ethyl)pyr imidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(5-fluoro-2,7- dimethylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.96 min; [M+H] ⁺ = 320.06 .

B.1.3.1. 2-(5-Fluoro-2,7-dimethylbenzofuran-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 5-fluoro-2,7- dimethylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.61 min; [M+H] ⁺ = 208.14 .

B.1.3.2. 5-Fluoro-2,7-dimethylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 5-fluoro-2,7- dimethylbenzofuran. LC-MS A: t _R = 0.87 min; no ionization.

B.1.3.3. 5-Fluoro-2,7-dimethylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 5-fluoro-2- hydroxy-3-methylbenzaldehyde. LC-MS A: t _R = 0.92 min; no ionization.

B.1.4. 6-Chloro-N-(2-(2-ethyl-5-fluoro-7-methylbenzofuran-3-yl)ethy l)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(2-ethyl-5-fluoro-7- methylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.99 min; [M+H] ⁺ = 333.97 .

B.1.4.1. 2-(2-Ethyl-5-fluoro-7-methylbenzofuran-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 2-ethyl-5- fluoro-7-methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.65 min; [M+H] ⁺ = 222.06 .

B.1.4.2. 2-Ethyl-5-fluoro-7-methylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 2-ethyl-5- fluoro-7-methylbenzofuran. LC-MS A: t _R = 0.91 min; no ionization. B.1.4.3. 2-Ethyl-5-fluoro-7-methylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 5-fluoro-2- hydroxy-3-methylbenzaldehyde and methyl 2-bromobutanoate. LC-MS A: t _R = 0.96 min; no ionization.

B.1.5. 6-Chloro-N-(2-(5-chloro-2J-dimethylbenzofuran-3-yl)ethyl)pyr imidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(5-chloro-2,7- dimethylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.99 min; [M+H] ⁺ = 336.18 .

B.1.5.1. 2-(5-Chloro-2,7-dimethylbenzofuran-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 5-chloro- 2,7-dimethylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.66 min; [M+H] ⁺ = 223.69 .

B.1.5.2. 5-Chloro-2,7-dimethylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 5-chloro- 2,7-dimethylbenzofuran. LC-MS A: t _R = 0.90 min; no ionization.

B.1.5.3. 5-Chloro-2,7-dimethylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 5-chloro-2- hydroxy-3-methylbenzaldehyde. LC-MS A: t _R = 0.95 min; no ionization.

B.1.6. 6-Chloro-N-(2-(5J-dichloro-2-methylbenzofuran-3-yl)ethyl)pyr imidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(5,7-dichloro-2- methylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 1.00 min; [M+H] ⁺ = 355.99 .

B.1.6.1. 2-(5,7-Dichloro-2-methy I benzof uran-3-yl)ethan-1 -amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 5,7-dichloro-

2-methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.66 min; no ionization.

B.1.6.2. 5,7-Dichloro-2-methylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 5,7-dichloro- 2-methylbenzofuran. LC-MS A: t _R = 0.92 min; no ionization.

B.1.6.3. 5,7-Dichloro-2-methylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 3,5-dichloro- 2-hydroxybenzaldehyde. LC-MS A: t _R = 0.96 min; no ionization.

B.1.7. 6-Chloro-N-(2-(5-chloro-7-methoxy-2-methylbenzofuran-3-yl)et hyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(5-chloro-7-methoxy- 2-methylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.95 min; [M+H] ⁺ = 352.10 .

B.1.7.1. 2-(5-Chloro-7-methoxy-2-methylbenzofuran-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 5-chloro-7- methoxy-2-methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.60 min; [M+H] ⁺ = 240.17 . B.1.7.2. 5-Chloro-7-methoxy-2-methylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 5-chloro-7- methoxy-2-methylbenzofuran. LC-MS A: t _R = 0.90 min; [M+H] ⁺ = 225.01 .

B.1.7.3. 5-Chloro-7-methoxy-2-methylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 5-chloro-2- hydroxy-3-methoxybenzaldehyde. LC-MS A: tR = 0.92 min; no ionization.

B.1.8. 6-Chloro-N-(2-(4,5-difluoro-7-methoxy-2-methylbenzofuran -yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(4,5-difluoro-7- methoxy-2-methylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.95 min; [M+H] ⁺ = 353.95 .

B.1.8.1. 2-(4,5-Difluoro-7-methoxy-2-methylbenzofuran-3-yl)ethan-1-am ine

The title compound is prepared according to the procedure described above in B.1.1.1. using 4,5-difluoro- 7-methoxy-2-methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.61 min; [M+H] ⁺ = 242.02 .

B.1.8.2. 4,5-Difluoro-7-methoxy-2-methylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 4,5-difluoro- 7-methoxy-2-methylbenzofuran. LC-MS A: t _R = 0.86 min; [M+H] ⁺ = 227.06 .

B.1.8.3. 4,5-Difluoro-7-methoxy-2-methylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 2,3-difluoro- 6-hydroxy-5-methoxybenzaldehyde. LC-MS A: t _R = 0.91 min; no ionization.

B.1.8.4. 2,3-Difluoro-6-hydroxy-5-methoxybenzaldehyde

To a cooled (-78°C) solution of 2,3-difluoro-5,6-dimethoxybenzaldehyde (1.14 g, 5.63 mmol) in anh. DCM (10 mL) is added dropwise a solution of boron trichloride (1 M in DCM, 6.2 mL, 6.2 mmol) and the RM is further stirred at -78°C, under nitrogen, for 10 min and then at RT for 16h. The RM is cooled (0°C), treated carefully with water (10 mL) and stirred at RT for 1.5h. Water and DCM are added and the layers are separated. The aq. layer is extracted twice with DCM and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording 2,3-difluoro-6-hydroxy-5- methoxybenzaldehyde as a yellow solid (0.97 g, 91 %). LC-MS A: t _R = 0.73 min; no ionization.

B.1.8.5. 2,3-Difluoro-5,6-dimethoxybenzaldehyde

To a cooled (-78°C) solution of 1 ,2-difluoro-4,5-dimethoxybenzene (1.00 g, 5.74 mmol) in anh. THF (20 mL) is added dropwise a solution of n-butyllithium (2.5 M in hexanes, 2.53 mL, 6.32 mmol) and the RM is further stirred at -78°C, under nitrogen, for 1 h. Anh. DMF (0.667 mL, 8.61 mmol) is then added dropwise to the previous mixture and stirring at -78°C is continued for 3h. The RM is treated carefully with sat. aq. NH4CI (50 mL). Water (50 mL) and EtOAc (100 mL) are then added and the layers are separated. The aq. layer is further extracted with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording 2,3-difluoro-5,6-dimethoxybenzaldehyde as a yellow solid (1.14 g, 98%). LC-MS A: t _R = 0.77 min; [M+H] ⁺ = 203.10 .

B.1.9. 6-Chloro-N-(2-(4-fluoro-7-methoxy-2-methylbenzofuran -yl)ethyl)pyrimidin-4-amine

The title compound is prepared according to the procedure described above in B.1.1. using 2-(4-fluoro-7-methoxy- 2-methylbenzofuran-3-yl)ethan-1 -amine. LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 335.93 .

B.1.9.1. 2-(4-Fluoro-7-methoxy-2-methylbenzofuran-3-yl)ethan-1-amine

The title compound is prepared according to the procedure described above in B.1.1.1. using 4-fluoro-7- methoxy-2-methylbenzofuran-3-carbaldehyde. LC-MS A: t _R = 0.58 min; [M+H] ⁺ = 223.90 .

B.1.9.2. 4-Fluoro-7-methoxy-2-methylbenzofuran-3-carbaldehyde

The title compound is prepared according to the procedure described above in B.1.1.2. using 4-fluoro-7- methoxy-2-methylbenzofuran. LC-MS A: t _R = 0.82 min; no ionization.

B.1.9.3. 4-Fluoro-7-methoxy-2-methylbenzofuran

The title compound is prepared according to the procedure described above in B.1.1.3. using 6-fluoro-2- hydroxy-3-methoxybenzaldehyde. LC-MS A: t _R = 0.88 min; no ionization.

B.1.9.4. 6-Fluoro-2-hydroxy-3-methoxybenzaldehyde

The title compound is prepared according to the procedure described above in B.1.8.4. using 6-fluoro-2,3- dimethoxybenzaldehyde. LC-MS A: t _R = 0.69 min; no ionization.

B.1.9.5. 6-Fluoro-2,3-dimethoxybenzaldehyde

The title compound is prepared according to the procedure described above in B.1.8.5. using 4-fluoro-1 ,2- dimethoxybenzene. LC-MS A: t _R = 0.71 min; [M+H] ⁺ = 185.23 .

C- Synthesis of boronic acid derivatives of formula (A4)

C.1.1. 5-(4,4,5,5-Tetramethyl-1 ,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)thiophene-2-carbo xylic acid

Lithium diisopropylamide solution (2.0 M in THF/hexanes, 2.53 mL, 5.05 mmol) is added dropwise to a solution of 3-(trifluoromethyl)thiophene-2-carboxylic acid (330 mg, 1.68 mmol) in THF (7 mL) at -78°C. The RM is stirred for 30 min at -78°C then at 0°C for 10 min. Back at -78°C, a solution of 2-isopropoxy-4,4,5,5-tetramethyl-1 ,3,2- dioxaborolane (0.771 mL, 3.7 mmol) in THF (15 mL) is added dropwise and the RM is slowly allowed to warm to RT overnight. HCI 0.5N (20 mL) is added and the mixture is extracted with EtOAc. The combined organic layers are washed with brine, dried over MgSC>4 and the solvent is removed. The crude product is purified by FC (DCM/MeOH 1 :0 to 19:1 ) to afford the title compound as a light orange solid (443 mg, 82%). LC-MS A: t _R = 0.59 min; no ionization.

C.1.1.1. 3-(Trifluoromethyl)thiophene-2-carboxylic acid To a -78°C solution of 3-(trifluoromethyl)thiophene (0.4 mL, 3.68 mmol) in dry THF (10 mL) is added dropwise a solution of butyllithium (1.38M in hexane, 2.93 mL, 4.05 mmol) and the RM is stirred for 30 min. The RM is then poured over an excess of freshly crushed dry ice carbon dioxide. Once the RM is back at RT, HC1 1 N is added until pH<3 and the mixture is extracted with DCM (3x). The organic layer is dried over MgSC>4 and concentrated under vacuum, affording the title compound as a pale yellow solid (0.72 g, quantitative). LC-MS

A: t _R = 0.69 min; no ionization.

C.1.2. 3-Ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid

The title compound is prepared according to the synthesis of C.1.1. using 3-ethoxythiophene-2-carboxylic acid. LC- MS A: t _R = 0.48 min; [M+H] ⁺ = 217.07 (boronic acid, from hydrolysis of the pinacol ester on the LC-MS-column). C.1.3. 5-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)-1 H-tetrazole

A mixture of 2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile (500 mg, 1.83 mmol), Azidotributyltin(IV) (0.768 mL, 2.75 mmol), and dry toluene (4 mL) is heated at 180°C for 1 h under MW irradiation. The mixture is cooled to RT, treated with HCI 0.1 N and extracted with EtOAc. The organic layer is dried over MgSC>4 and concentrated under vacuum. The residue is purified via FC, eluting with a gradient from Heptane:EtOAc 100:0 to 10:90. This affords the title compound as a white solid (135 mg, 23%). LC-MS B: t _R = 0.87 min; [M+H]+ = 317.14.

C.1.3.1. 2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benz onitrile

A solution of 2-hydroxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile (1.50 g, 6.12 mmol), K2CO3 (1.69 g, 12.2 mmol) in DMF (4 mL) and iodoethane (0.596 mL, 7.34 mmol) is heated at 120°C for 30 min. The RM is cooled down to RT, partitioned between DCM and 1 N NaHC03. The aqueous layer is re-extracted with DCM, the combined organics are dried (MgS04), and concentrated under reduced pressure. This affords the title compound as a beige solid (1.31 g, 78%). LC-MS B: t _R = 0.96 min; [M+MeCN+H] ⁺ = 315.10.

C.1.4. 2-(Difluoromethoxy)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoic acid

To a solution of 4-bromo-2-(difluoromethoxy)benzoic acid (1.00 g, 3.56 mmol) in DMF (20 mL) are added at RT bis(pinacolato)diboron (1.355 g, 5.34 mmol), KOAc (1.047 g, 10.7 mmol) and 1 ,1'-bis(diphenylphosphino)ferrocene dichloropalladium(ll) (208 mg, 0.285 mmol). The RM is stirred at 100°C for 17h, then cooled to RT and filtered through a pad of celite, washing with EtOAC. The filtrate is washed with water and the aqueous layer is extrated (x2) with EtOAc. Organic layers are combined, washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. The residue is purified by FC eluting with DCM to afford the title compound as an orange solid (846 mg, 76%). LC-MS A: t _R = 0.37 min; [M+H] ⁺ = 313.1 1.

Following the procedure described for the synthesis of C.1.4. described above, the following boronic acid derivatives are synthesized, starting from the corresponding halides (see table 3). Table 3: Boronic acid derivatives C.1.5. - C.1.8.

C.1.9. 2-Fluoro-6-propyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan- 2-yl)benzoic acid

The title compound is prepared according to the procedure described for C.1.4. starting with 4-bromo-2-fluoro-6- propylbenzoic acid. LC-MS E: t _R = 0.48 min; [M-H] ⁺ = 307.11.

C.1.9.1. 4-Bromo-2-fluoro-6-propylbenzoic acid

To a solution of 4-bromo-2,6-difluorobenzoic acid (5.00 g, 21.1 mmol) in THF (50 mL) at 0°C is added dropwise over 30 min n-propylmagnesium bromide (2M in THF, 21.6 mL, 43.2 mmol). The RM is allowed to reach RT and stirred for 17h, then quenched carefully at 0°C with MeOH (10 mL). After stirring for 5 min, the solvent is removed under reduced pressure. The residue is partitioned between EtOAc and 2N HCI. The aqueous phase is re-extracted with EtOAc (2x). The combined org. phases are washed with water, brine, dried over MgS0 ₄ , filtered and concentrated. The residue is purified by FC (heptane/EtOAc 100:0 to 70:30) to afford the title compound as a white solid (4.45 g, 81 %). LC-MS A: tR = 0.84 min; no ionization.

C.1.10. 2-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenoxy)acetic acid

A solution of ethyl 2-(2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenoxy)acetate (1.285 g, 3.82 mmol) in EtOH (15 mL) is treated with NaOH 10% (7.64 mL, 19.1 mmol) and the RM is stirred at 50°C for 30 min. The RM is cooled to RT and diluted with EtOAc. HCI 2N (15 mL) is added to reach acidic pH (<1 ). The aqueous layer is extracted twice with EtOAc. The resulting organic phase is dried over MgS04 and concentrated, affording the title compound as an orange paste. LC-MS A: t _R = 0.80 min; [M+H] ⁺ = 323.12.

C.1.10.1. Ethyl 2-(2-ethoxy-4-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate

A solution of 2-eth oxy-4-(4 ,4,5, 5-te tram eth y I - 1 ,3,2-dioxaborolan-2-yl)phenol (3.47 g, 12.5 mmol) in anhydrous DMF (50 mL) is treated successively with cesium carbonate (6.10 g, 18.7 mmol) and ethyl bromoacetate (1.48 mL, 13.1 mmol). The RM is stirred at RT for 1 h. Water is added, and the mixture is extracted with Et20 (x 3). The combined organic layers are then washed successively with water (x 2) and brine, dried over MgS04, filtered, and concentrated to dryness under reduced pressure to afford the pure product as a colorless oil (1.46g, 77%). LC-MS A: t _R = 0.94 min; [M+H] ⁺ = 351.18.

C.1.11. (2-Ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)glycine

To a solution of methyl (2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)glycinate (207 mg, 0.61 mmol) in THF/H ₂ 0 (4:1 ) (5 mL) is added LiOH.H ₂ 0 (51 mg, 1.21 mmol) and the mixture is stirred at RT for 2h. The mixture is treated with HC1 1 N (1 mL) and extracted with EtOAc, dried over MgSC>4 and concentrated, affording the title compound as a brown oil (0.151 g, 78%). LC-MS A: t _R = 0.82 min; [M+H] ⁺ = 322.07.

C.1.11.1. Methyl (2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)glycinate

The title compound is prepared according to the procedure described for C.1.4., starting with methyl (4-bromo- 2-ethoxyphenyl)glycinate. LC-MS A: t _R = 0.93 min; [M+H] ⁺ = 336.28.

C.1.11.2. Methyl (4-bromo-2-ethoxyphenyl)glycinate

To a solution of 4-bromo-2-ethoxyaniline (0.60 g, 2.64 mmol) in DMF (2.5 mL) is added DiPEA (0.673 mL, 3.96 mmol) followed by methyl bromoacetate (0.275 mL, 2.9 mmol). The mixture is stirred at 90°C for 1 h in the MW apparatus. The DMF is evaporated under high vacuum and the residue is purified by FC, eluting with Hept/EtOAc 1 :0 to 17:3 affording the title compound as a dark red oil (0.71 g, 94%). LC-MS A: t _R = 0.89 min;

[M+H] ⁺ = 288.08.

C.1.12. 3-(2-Ethoxy-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)-[1,2,4]oxadiazol-5(4H)-one

The title compound is prepared according to the procedure described for C.1.4., starting with 3-(4-bromo-2- ethoxyphenyl)-[1 ,2,4]oxadiazol-5(4H)-one. LC-MS A: t _R = 0.89 min; [M+H] ⁺ = 333.06.

C.1.12.1. 3-(4-Bromo-2-ethoxyphenyl)-[1 ,2,4]oxadiazol-5(4H)-one

A solution of 4-bromo-2-ethoxy-N'-hydroxybenzimidamide (1.395 g, 5.38 mmol), 1 , 1 '-carbonyldiimidazole (1.31 g, 8.08 mmol) and 1 ,8-diazabicyclo[5.4.0]undec-7-ene (1.23 mL, 8.08 mmol) in dioxane (20 mL) is stirred at 90°C for 4h30min. Once at RT, the product precipitated upon addition of HCI 1 M. Dioxane is partially evaporated via N2 stream prior to filtering off the solid under vacuum, washing with water. The title compound is obtained as a white solid (1.375 g, 90%). LC-MS A: t _R = 0.81 min, [M+MeCN] ⁺ = 325.89.

C.1.12.2. 4-Bromo-2-ethoxy-N'-hydroxybenzimidamide

A suspension of 4-bromo-2-ethoxybenzonitrile (1.50 g, 6.5 mmol), hydroxylamine hydrochloride (913 mg, 13 mmol) and NaHCOs (1.365 g, 16.3 mmol) in water (1.32 mL) and EtOH (26.6 mL) is stirred in a sealed tube at 90 °C for 3h. Once at RT, the product precipitated from the RM upon addition of water. The solid is filtered off under high vacuum, washing with water and some Et20. A first crop of pure title compound (947mg) is thus obtained as white solid. The filtrate is extracted with EtOAc. The organic layer is then washed twice with brine, dried over MgS04, filtered and concentrated. The residue is purified by FC (hept EtOAc 5:5) to yield another crop of the pure title compound as a white solid (448 mg), merged with the first batch from precipitation. The title compound is obtained as a white solid (1.395 g, 83%). LC-MS A: t _R = 0.53 min, [M+H] ⁺ = 259.03.

C.1.13. 3-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henoxy)propanoic acid

The title compound is prepared according to the procedure described for C.1.4., starting with 3-(4-bromo-2- ethoxyphenoxy)propanoic acid. LC-MS E: t _R = 0.45 min; [M-H] ⁺ = 335.18.

C.1.13.1. 3-(4-Bromo-2-ethoxyphenoxy)propanoic acid

A MW vial is charged with 4-bromo-2-ethoxyphenol (1300 mg, 5.98 mmol), H ₂ 0 (5 mL), NaOH 32% (1.332 mL, 14.38 mmol) and 3-chloropropionic acid (674 mg, 6.08 mmol). It is sealed and irradiated at 120°C, for 40 min at high energy level. The RM is diluted in water and pH is decreased to pH9 with HCI 2N then is extracted twice with EtOAc. The basic aqueous layer is then acidified to pH2 and extracted twice with EtOA, the combined organic extracts are washed with water, brine, dried over MgSC>4, filtered and evaporated to dryness, yielding the title compound as a a white powder (0.448 g, 56%). LC-MS B: t _R = 0.89 min; [M+H] ⁺ = 289.10.

C.1.14. Methyl (EJ-3-(3-ethoxy-5-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acrylate

The title compound is prepared according to the procedure described for C.1.1 starting with methyl (ξ)-3-(3- ethoxythiophen-2-yl)acrylate. LC-MS A: t _R = 1.02 min; [M+H] ⁺ = 339.14.

C.1.14.1. Methyl (EJ-3-(3-ethoxythiophen-2-yl)acrylate

A suspension of 3-ethoxythiophene-2-carbaldehyde (2.90 g, 18.6 mmol), methyl bromoacetate (3.07 mL, 33.4 mmol), and triphenylphosphine (7.305 g, 27.8 mmol ) in aq saturated NaHCC>3 (100 mL) is stirred at RT for 5h. THF (30 mL) is added and the RM is stirred overnight at RT. It is then extracted twice with DCM. The combined organic layers are dried over MgSC>4, filtered, and concentrated under vacuum. The crude is purified by FC (Hept/EtOAc 9:1 ) to afford the title compound as a dark orange oil (2.9 g, 100%). LC-MS A: t _R = 0.69 min; [M+MeCN] ⁺ = 198.26.

C.1.15. 3-(3-Ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)propanoic acid

To a solution of methyl (E)-3-(3-ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acrylate [C.1.14.] (250 mg, 0.786 mmol) in MeOH (15 mL) is added Pd/C 5% wet (50 mg). Then the vessel is inertized with N2 and flushed with H2. The mixture is placed in a autoclave and it is stirred overnight at RT under 4 Bar of H2, then for 1 d at 50°C under 4 bar of H ₂ . After filtration on whatman filter, NaOH 10% (1.18 mL, 1 1.8 mmol) is added and the RM is stirred for 1 h at RT. It is then treated with HCI 2N until pH<1 and extracted twice with EtOAc. The organic layer is dried over MgS04 and concentrated, to afford the title compound as a dark yellow oil (287 mg, 74%). LC- MS A: t _R = 0.86 min; [M+H] ⁺ = 327.09.

C.1.16. Methyl 2-(3-ethoxy-5-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)ac etate A suspension of methyl 2-(3-ethoxythiophen-2-yl)acetate (815 mg, 4.07 mmol), bis(pinacolato)diboron (633 mg, 2.44 mmol), (1 ,5-cyclooctadiene)(methoxy)iridium(l) dimer (28.9 mg, 0.0437 mmol) and 4,4'-di-tert-butyl-2,2'- dipyridyl (26.8 mg, 0.0999 mmol) in THF (19.3 mL) is degassed with a nitrogen stream for 15min and then stirred at 80°C overnight. The RM is concentrated under reduced pressure and the residue is purified by FC (Hept to Hept/EtOAc 9:1 ) to afford the title compound as a colourless oil which crystallized upon standing. LC-MS B: tR = 1.03 min; [M+H] ⁺ = 327.14.

C.1.16.1. Methyl 2-(3-ethoxythiophen-2-yl)acetate

Silver benzoate (1800 mg, 7.78 mmol) is added portionwise to a solution of 2-diazo-1-(3-ethoxythiophen-2- yl)ethan-1 -one (2025 mg, 10.3 mmol) and TEA (4.31 mL, 31 mmol) in MeOH (52.7 mL) and the RM is stirred at RT for 2h. It is then diluted with EtOAc and filtered over celite. The filtrate is washed twice with sat. aq. NaHC03 and once with brine. The organic layer is dried over MgSC>4, filtered and concentrated. The residue is purified by FC (Hept to Hept EtOAc 95:5) to yield the title compound as a light yellow oil (817 mg, 40%). LC-MS B: tR = 0.86 min, [M+H] ⁺ = 201.14.

C.1.16.2. 2-Diazo-1 -(3-ethoxythiophen-2-y l)ethan-1 -one

A solution of 3-ethoxythiophene-2-carboxylicacid (2500 mg, 14.1 mmol) in DCM (120 mL) is treated with thionyl chloride (1.56 mL, 21.1 mmol), dropwise. The RM is stirred at RT overnight, it is then concentrated in vacuo, and the residue is dissolved in MeCN (80 mL). TEA (2.2 mL, 15.8 mmol) is added dropwise and the solution is cooled down to 0°C. (Trimethylsilyl)diazomethane (2M solution, 15 mL, 30 mmol) is added dropwise and the RM is stirred at RT for 2d. It is then carefully quenched by dropwise addition of AcOH, until no more bubbling is observed. The RM is then concentrated and the residue is partitioned between EtOAc and water. The organic layer is then washed with sat. aq. NaHC0 ₃ and with brine, dried (MgSCXi) and concentrated. The residue is purified by FC (Hept to Hept EtOAc 8:2) to yield the title compound as an intense yellow solid (2.028 g, 73%). LC-MS B: t _R = 0.78min, [M+H] ⁺ = 197.15.

C.1.17. Ethyl 2-((2-ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)amino)-2-oxoacetate

The title compound is prepared according to the procedure described for C.1.4., starting with ethyl 2-((4-bromo-2- ethoxyphenyl)amino)-2-oxoacetate. LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 364.21.

C.1.17.1. Ethyl 2-((4-bromo-2-ethoxyphenyl)amino)-2-oxoacetate

To a solution of 4-bromo-2-ethoxyaniline (1.10 g, 4.84 mmol) in DCM (35 mL) is added TEA (0.748 mL, 5.32 mmol) at RT. The RM is cooled to 0°C and ethyl oxalyl chloride (0.61 mL, 5.32 mmol) is added dropwise. The RM is stirred for 30 min at 0°C then allowed to warm to RT and stirred for 30 min. The RM is partitioned between ethyl acetate and saturated aqueous solution of NaHCC>3. The two layers are separated and the organic layers washed with water, brine then dried over MgSC>4, filtered and solvent removed under vacuo, affording the title compound as a brown solid (1.52 g, 99%). LC-MS A: t _R = 0.92 min; [M+MeCN] ⁺ = 316.04.

C.1.18. 2-Butoxy-6-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoic acid The title compound is prepared according to the procedure described for C.2.4., starting with 4-bromo-2-butoxy-6- fluorobenzoic acid. LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 339.21.

C.1.18.1. 4-Bromo-2-butoxy-6-fluorobenzoic acid

Methyl 4-bromo-2-butoxy-6-fluorobenzoate (1246 mg, 3.94 mmol) is dissolved in EtOH (15 mL). NaOH 32% (1.82 mL, 19.7 mmol) is added and the RM is heated up to 60°C for 1 h. it is then cooled to RT and diluted with EtOAc. HCI 2N (10 mL) is added to reach acidic pH (<2). The aq. layer is extracted twice with EtOAc. The resulting organic phase is dried over MgSC>4 and concentrated, affording the title compound as a white solid. LC-MS E: t _R = 0.52 min; [M-H] ⁺ = 290.89.

C.1.18.2. Methyl 4-bromo-2-butoxy-6-fluorobenzoate

To a solution of methyl 4-bromo-2-fluoro-6-hydroxybenzoate (1.00 g, 4.02 mmol) in DMF (10 mL), is added

Cs ₂ C0 ₃ (2.62 g, 8.03 mmol) followed by 1-iodobutane (0.685 mL, 6.02 mmol). The RM is stirred at 120°C for 2h in the MW. The RM is concentrated under reduced pressure, the residue is partitioned between DCM and water. The aqueous layer is re-extracted with DCM, the combined organics are dried (MgSC>4), and concentrated under reduced pressure. Purification by FC (Hept EtOAc 1 :0 to 19:1 ) affords the title compound as a colourless oil (1.24 g, 99%). LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 306.84.

C.1.19. Propyl 2-(propylthio)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-y l)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with propyl 4-bromo-2- (propylthio)benzoate. LC-MS A: t _R = 1.06 min; [M+H] ⁺ = 365.04.

C.1.19.1. Propyl 4-bromo-2-(propylthio)benzoate

Propyl iodide (1.51 mL, 15.3 mmol) is added dropwise to a 0°C solution of 4-bromo-2-sulfanylbenzoic acid

(1.50 g, 6.1 1 mmol) and Cs ₂ C0 ₃ (4.18 g, 12.8 mmol) in DMF (60 mL). The RM is stirred for 15 min at 0°C and then at RT for 16h. The RM is quenched with water, then EtOAc is added and layers are separated. The aqueous layer is extracted twice with EtOAc. The combined organic layers are washed with brine, dried (MgS04), and concentrated under reduced pressure. The residue is purified by FC, eluting with Heptane to give the title compound as a pale yellow solid (1.66 g, 86%). LC-MS A: t _R = 1.04 min; no ionization.

C.1.20. Isopropyl 2-(isopropylthio)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan- 2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4, starting with isopropyl 4-bromo-2- (isopropylthio)benzoate. LC-MS A: t _R = 1.06 min; [M+H] ⁺ = 365.21.

C.1.20.1. Isopropyl 4-bromo-2-(isopropylthio)benzoate

The title compound is prepared according to the procedure described C.1.19.1., using isopropyl iodide. LC- MS A: t _R = 1.04 min; no ionization. C.1.21. Cyclobutyl 2-(cyclobutylthio)-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with cyclobutyl 4-bromo- 2-(cyclobutylthio)benzoate. LC-MS A: to = 1.10 min; [M+H] ⁺ = 389.26.

C.1.21.1. Cyclobutyl 4-bromo-2-(cyclobutylthio)benzoate

The title compound is prepared according to the procedure described for C.1.19., using bromocyclobutane.

LC-MS A: t _R = 1.07 min; no ionization.

C.1.22. Methyl 2-ethoxy-6-methyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with 4-bromo-2-ethoxy-6- methylbenzoic acid. LC-MS A: t _R = 0.97 min; [M+H] ⁺ = 321.16.

C.1.22.1. Methyl 4-bromo-2-ethoxy-6-methylbenzoate

A mixture of methyl 4-bromo-2-hydroxy-6-methylbenzoate (600 mg, 2.45 mmol), CS2CO3 (1994 mg, 6.12 mmol) and iodoethane (0.435 mL, 5.39 mmol) in DMF (4 mL) is stirred at 130°C for 3h. Once cooled down at RT, water is added and the RM is extracted with EfeO. The organic layer is successively washed with water and brine, dried over MgSC>4 and concentrated under reduced pressure. The residue is purified by FC (Heptane/EtOAc 7/3), affording the title compound as a yellow oil (595 mg, 89%). LC-MS A: t _R = 0.91 min;

[M+H] ⁺ = 273.05.

C.1.23. Methyl 2-(cyclopentyloxy)-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with methyl 5-bromo-2- (cyclopentyloxy)benzoate. LC-MS A: t _R = 1.01 min; [M+H] ⁺ = 347.15.

C.1.23.1. Methyl 5-bromo-2-(cyclopentyloxy)benzoate

To a solution of methyl 4-bromo-2-hydroxybenzoate (2.00 g, 8.4 mmol) in DMF (20 mL), bromocyclobutane (1.01 mL, 9.24 mmol) and K2CO3 (1.74 g, 12.6 mmol) aere added. The RM is stirred at 80°C for 19h, cooled to RT, and partitioned between water and EbO. Organic layers are combined and washed with additional water, dried over MgS04 and concentrated to dryness. The crude product is purified by FC, eluting with Heptane/DCM (100:0 to 40:60) to the product as a colourless oil (1.88 g, 75%). LC-MS A: t _R = 0.97 min;

[M+H] ⁺ = 298.89.

C.1.24. Methyl 2-fluoro-6-(methylthio)-4-(4,4,5,5-tetramethyl-1,3,2-dioxabo rolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., using methyl 4-bromo-2-fluoro-6- (methylthio)benzoate. LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 327.1 1.

C.1.24.1. Methyl 4-bromo-2-fluoro-6-(methylthio)benzoate

lodomethane (0.1 13 mL, 1.81 mmol) is added dropwise to a solution of 4-bromo-2-fluoro-6- (methylthio)benzoic acid (500 mg,1.51 mmol) and CS2CO3 (492 mg, 1.51 mmol) in anhydrous DMF (20 mL) at 0°C. The RM is stirred for 15 min at 0°C and then at RT for 1 h. It is quenched with water, then EtOAc is added and layers are separated. The aqueous layer is extracted twice with EtOAc. The organic layers are combined and washed with brine, dried over anhydrous MgS0 ₄ , filtered and concentrated under reduced. The crude product is purified by FC, eluting with heptane to give the title compound as a colorless oil (173 mg, 41 %). LC-MS A: t _R = 0.90 min; no ionization.

C.1.24.2. 4-Bromo-2-fluoro-6-(methylthio)benzoic acid

To a suspension of freshly powdered sodium hydroxide (397 mg, 9.92 mmol) in DMF (20 mL) at 0° is added 4-bromo-2,6-difluorobenzoic acid (2.00 g, 8.27 mmol, 1 eq) and the RM is stirred at 0°C for 10 min. Sodium thiomethoxide (732 mg, 9.92 mmol) is added and the resulting RM is allowed to warm up to RT and stirred for 2h. It is quenched with 2N HCI, and extracted with EtOAc (3x). The combined organic layers are washed with brine, dried over anhydrous MgSC>4, filtered and concentrated under reduced pressure to give the crude product quantitatively as a yellow oil. LC-MS A: tR = 0.76 min; no ionization.

C.1.25. Methyl 2-chloro-6-(methylthio)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., using methyl 4-bromo-2-fluoro-6- (methylthio)benzoate. LC-MS A: t _R = 1.00 min; [M+H] ⁺ = 343.14.

C.1.25.1. Methyl 4-bromo-2-chloro-6-(methylthio)benzoate

The title compound is prepared according to the procedure described for C.1.24.1., using 4-bromo-2-chloro- 6-(methylthio)benzoic acid. LC-MS A: tR = 0.93 min; no ionization.

C.1.25.2. 4-Bromo-2-chloro-6-(methylthio)benzoic acid

The title compound is prepared according to the procedure described for C.1.24.2., using 4-bromo-2-fluoro-

6-chlorobenzoic acid. LC-MS A: tR = 0.77 min; no ionization.

C.1.26. 5-(4-(4,4,5 _! 5-Tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)-[1 ,2,4-]oxadiazol-3-ol

The title compound is prepared according to the procedure described for C.1.4., using 5-(4-bromophenyl)- [1 ,2,4]oxadiazol-3-ol. LC-MS A: t _R = 0.82 min; [M+H] ⁺ = 290.10.

C.1.27. Methyl 2-(2-hydroxyethoxy)-4-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with methyl 4-bromo-2-(2- hydroxyethoxy)benzoate. LC-MS B: t _R = 0.89 min; [M+H] ⁺ = 323.26.

C.1.27.1. Methyl 4-bromo-2-(2-hydroxyethoxy)benzoate

NaH (101 mg, 4.2 mmol) is added portionwise to a 0°C solution of methyl 4-bromo-2-hydroxybenzoate (500 mg, 2.1 mmol) in DMF (5 mL). The RM is stirred for a few minutes at 0°C, then 2-bromoethanol (0.235 mL,

3.15 mmol) is added and the RM is stirred at 90°C for 2h45, then cooled to RT. Water is added to the RM and it is extracted twice with EtOAc. The combined organic layers are washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. The residue is purified by FC (heptane/EtOAc, 1 :0 to 6:4), affording the title compound as a colorless oil (358 mg, 62%). LC-MS B: t _R = 0.77 min; [M+H] ⁺ = 275.14.

C.1.28. 7-(4,4,5 _! 5-Tetramethyl-1 ,3 _! 2-dioxaborolan-2-yl)-2,3-dihydro-5H-thieno[3 _! 2-e][1 ,4]dioxepin-5-one

The title compound is prepared according to the procedure described for C.1.16.., starting with 2,3-dihydro-5H- thieno[3,2-e][1 ,4]dioxepin-5-one. LC-MS B: t _R = 0.51 min; [M+H] ⁺ = 215.41 (mass from boronic acid from pinacol ester cleavage during LC-MS analysis).

C.1.28.1. 2,3-Dihydro-5H-thieno[3,2-e][1,4]dioxepin-5-one

A MW vial is charged with K2CO3 (623 mg, 4.5 mmol), methyl 3-hydroxythiophene-2-carboxylate (250 mg, 1.5 mmol) and DMF (5 mL). The RM is stirred for a few minutes then 2-bromoethanol (0.146 mL, 1.95 mmol) is added, the vial is capped and heated at 100°C fo 2h under MW irradiation. 2-Bromoethanol (0.0319 mL,

0.45 mmol) is added and the RM is stirred at 90°C overnight, under thermal conditions. Once at RT, water is added and the RM is extracted thrice with EtOAc. The combined organic layers are dried over MgSC>4, filtered and concentrated under reduced pressure, affording the crude title compound as a brownish solid (338 mg, quantitative). LC-MS B: t _R = 0.61 min; [M+H] ⁺ = 170.94.

C.1.29. methyl 2-cyclobutoxy-3-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

To a solution of methyl 4-bromo-2-cyclobutoxy-3-fluorobenzoate (435 mg, 1.44 mmol) in anh. DMF (7 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (547 mg, 2.15 mmol), potassium acetate (423 mg, 4.31 mmol) and [1 ,1 '-bis(diphenylphosphino)ferrocene]dichloropalladium(ll) (84 mg, 0.11 mmol). The RM is heated to 90°C, under nitrogen, for 14h. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with Et20. The filtrate is washed with water and the aqueous layer is extracted twice with Et20. The combined organic layers are then washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-cyclobutoxy-3-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate as a pale yellow solid (235 mg, 47%). LC-MS A: t _R = 1.01 min; [M+H] ⁺ = 351.27 .

C.1.29.1. methyl 4-bromo-2-cyclobutoxy-3-fluorobenzoate

To a solution of methyl 4-bromo-3-fluoro-2-hydroxybenzoate (553 mg, 2.22 mmol) in anh. DMF (30 mL) at RT is added cesium carbonate (1.085 g, 3.33 mmol) and the mixture is stirred at RT for 15 min. The mixture is then treated with bromocyclobutane (0.235 mL, 2.44 mmol) and the RM is heated to 80°C for 16h. The RM is allowed to cool to RT, water and Et20 are then added, and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated to dryness under reduced pressure. Purification by FC (heptane/DCM = 2/1 ) affords methyl 4-bromo-2-cyclobutoxy-3-fluorobenzoate as a pale yellow oil (435 mg, 65%). LC-MS A: t _R = 0.95 min; no ionization. C.1.29.2. methyl 4-bromo-3-fluoro-2-hydroxybenzoate

To a solution of 4-bromo-3-fluoro-2-hydroxybenzoic acid (800 mg, 3.40 mmol) in anh. DMF (6 mL) at RT is added potassium bicarbonate (409 mg, 4.08 mmol) and the mixture is stirred at RT for 5 min. The mixture is then treated with iodomethane (0.318 mL, 5.1 1 mmol) and the RM is heated to 40°C for 1.5h. The RM is allowed to cool to RT, water and Et20 are added, and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure affording methyl 4-bromo-3-fluoro- 2-hydroxybenzoate (553 mg, 65%). LC-MS A: t _R = 0.88 min; no ionization.

C.1.30. methyl 2-cyclobutoxy-6-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described above in C.1.29. using methyl 4-bromo-2- cyclobutoxy-6-fluorobenzoate. LC-MS A: t _R = 1.02 min; [M+H] ⁺ = 351.18 .

C.1.30.1. methyl 4-bromo-2-cyclobutoxy-6-fluorobenzoate

The title compound is prepared according to the procedure described above in C.1.29.1. using methyl 4- bromo-2-fluoro-6-hydroxybenzoate. LC-MS A: t _R = 0.96 min; no ionization.

C.1.31. oxetan-3-yl 2-(oxetan-3-ylthio)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described above in C.1.4. using oxetan-3-yl 4-bromo- 2-(oxetan-3-ylthio)benzoate. LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 393.20 .

C.1.31.1. oxetan-3-yl 4-bromo-2-(oxetan-3-ylthio)benzoate

To a cooled (0°C) mixture of 4-bromo-2-mercaptobenzoic acid (500 mg, 2.04 mmol) in anh. DMF (20 mL) is added cesium carbonate (1.394 g, 4.28 mmol) and the mixture is stirred at RT for 15 min. The cooled

(0°C) mixture is then treated with 3-bromooxetane (855 mg, 6.1 1 mmol) and the RM is heated to 85°C for 16h. The RM is allowed to cool to RT, water and EtOAc are then added, and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated to dryness under reduced pressure. Purification by FC (from heptane to tert-butyl methyl ether) affords oxetan-3-yl 4-bromo-2-(oxetan-3-ylthio)benzoate as a pale orange solid (229 mg, 33%). LC-MS A: t _R = 0.83 min; [M+H] ⁺ = 344.98.

C.1.32. Ethyl 2-(2-ethoxy-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)-2-oxoacetate

The title compound is prepared according to the procedure described for C.1.4., starting with ethyl 2-(4-bromo-2- ethoxyphenyl)-2-oxoacetate. LC-MS A: t _R = 0.98 min; [M+H] ⁺ = 349.19.

C.1.32.1. Ethyl 2-(4-bromo-2-ethoxyphenyl)-2-oxoacetate

To a solution of 2-(4-bromo-2-hydroxyphenyl)-2-oxoacetic acid (1.00 g, 3.88 mmol) and K2CO3 (1.605 g,) in DMF (10 mL) is added iodethane (0.799 mL, 9.69 mmol) and the RM is stirred at 50°C for 2 d. K2CO3 (1.605 g, 1 1.6 mmol) and iodethane (0.799 mL, 9.69 mmol) are added and the RM is stirred at 60°C for 20 h. The RM is filtered, rinsed with DCM and concentrated under reduced. The residue is purified by FC (HepLEtOAc 1 :0 to 4:1 ) to afford the title compound as a beige solid (0.921 g, 79%). LC-MS A: t _R = 0.92 min; [M+H] ⁺ = 303.03.

C.1.33. 3-Ethoxy-4-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)cyclobut-3-ene-1,2-dione

3-Ethoxy-4-(tributylstannyl)cyclobut-3-ene-1 ,2-dione (335 mg, 0.807 mmol) and 4-iodophenylboronic acid, pinacol ester (298 mg, 0.904 mmol) are dissolved in DMF (4 mL) with N2 bubbling for 5 min. Trans- Benzyl(chloro)bis(triphenylphosphine)palladium(ll) (36.7 mg, 0.0484 mmol) and Cul (15.4 mg, 0.0807 mmol) are added and the RM is stirred at RT for 3h., then filtered over a microglass filter, concentrated under vacuum and purified by FC (Hept:EtOAc 100:0 to 80:20) to obtain the title compound as a yellow solid (127 mg, 48%). LC-MS A: t _R = 0.97 min; [M+MeCN] ⁺ = 370.07.

C.1.34. 2-(2-Propoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetic acid

To a solution of propyl 2-(2-propoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate (308 mg, 0.85 mmol) in EtOH (9 mL) is added NaOH (10% aq. Solution, 3.4 mL) and the mixture is stirred at RT for 2h. EtOH is removed in vacuo. pH of the resulting basic aqueous layer is adjusted to pH=3-4 using HC1 1 N and extracted twice with EtOAc. The combined organic layers are washed with water, brine, dried over MgS04, filtered and solvent is removed in vacuo, yielding the title compound as a white powder (0.238 g, 87%). LC-MS A: t _R = 0.88 min; [M+H] ⁺ = 321.08.

C.1.34.1. Propyl 2-(2-propoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) phenyl)acetate

The title compound is prepared according to the procedure described for C.1.4., starting with propyl 2-(4- bromo-2-propoxyphenyl)acetate. LC-MS A: tR = 1.04 min; [M+H]+ = 363.12.

C.1.34.2. Propyl 2-(4-bromo-2-propoxyphenyl)acetate

To a solution of 4-bromo-2-hydroxyphenylacetic acid (1.50 g, 6.37 mmol,) in DMF (50 mL) is added 1 - iodopropane (1.38 mL, 14 mmol, 2.2 eq) and Cs ₂ C0 ₃ (6.23 g, 19.1 mmol). The RM is stirred at 100°C over night, then cooled to RT. Water is added, and the DMF is removed under reduced pressure. The residue is partitioned between EtOAc and water. The aqueous layer is re-extracted twice with EtOAc. The combined organic extracts are washed with brine, dried (MgS04) and concentrated in vacuo. The residue is purified by FC (HepLEtOAc 100:0 to 90:10), affording the title compound as a colourless oil (0.775 g, 39%). LC-MS A: t _R = 1.00 min; [M+H] ⁺ = 315.07.

C.1.35. 2-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henyl)acetic acid

Following the synthesis of C.1.34., with ethyl 2-(2-ethoxy -(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate, the title compound is obtained as a white solid. LC-MS B: t _R = 0.92 min; [M+H] ⁺ = 307.25.

C.1.35.1. Ethyl 2-(2-ethoxy-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

The title compound is prepared according to the procedure described for C.1.4., starting with ethyl 2-(4- bromo-2-ethoxyphenyl)acetate. LC-MS A: t _R = 1.01 min; [M+H] ⁺ = 287.04. C.1.35.2. Ethyl 2-(4-bromo-2-ethoxyphenyl)acetate

Following the synthesis of C.1.34.2., with 4-bromo-2-hydroxyphenylacetic acid and iodomethane, the title compound is obtained as a colorless oil. LC-MS B: t _R = 1.02 min; [M+H] ⁺ = 287.10.

C.1.36. 3-(4-(4,4,5,5-Tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)-[1 ,2,4]oxadiazol-5(4H)-one

The title compound is prepared according to the procedure described for C.1.4., starting with 3-(4-Bromophenyl)- [1 ,2,4]oxadiazol-5(4H)-one. LC-MS B: t _R = 0.90 min; [M+MeCN] ⁺ = 330.12.

C.1.37. N-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henyl)formamide

The title compound is prepared according to the procedure described for C.1.4., starting with N-(4-bromo-2- ethoxyphenyl)formamide. LC-MS B: t _R = 0.94 min; [M+H] ⁺ = 292.23.

C.1.37.1. N-(4-bromo-2-ethoxyphenyl)formamide

A mixture of 4-bromo-2-ethoxyaniline (1283 mg, 5.64 mmol), ethyl formate (18.5 mL, 226 mmol) and TEA (3.14 mL, 22.6 mmol) is stirred in a sealed tube at 85°C for 5 days. The RM is concentrated under reduced pressure. The residue is purified by FC (EtOAc:Hept 0:1 to 4:6) to afford the title compound as a brown solid (788 mg, 57%). LC-MS B: t _R = 0.84 min; [M+H] ⁺ = 285.06.

C.1.38. Isobutyl 2-(isobutylthio)-4-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

The title compound is prepared according to the procedure described for C.1.4., starting with isobutyl 4-bromo-2- (isobutylthio)benzoate. LC-MS A: t _R = 1.12 min; [M+H] ⁺ = 393.26.

C.1.38.1. Isobutyl 4-bromo-2-(isobutylthio)benzoate

The title compound is prepared according to the procedure described for C.1.4.1., using 4-bromo-2- sulfanylbenzoic acid and 1 -iodo-2-methylproprane. LC-MS A: t _R = 1.09 min; [M+H] ⁺ = 345.06.

C.1.39. 5-(2-Methoxy-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)isoxazol-3-ol

Butyllithium (1.6M in hexane, 1.1 mL, 1.76 mmol) is added dropwise , at -78 °C under nitrogen, to a stirred solution of 5-(4-bromo-2-methoxyphenyl)isoxazol-3-ol (158 mg, 0.585 mmol) in dry THF (4 mL). The RM is stirred at -78 °C for 25 min, then isopropoxyboronic acid, pinacol ester (0.418 mL, 2.05 mmol) is added dropwise and the RM is stirred at -78 °C for 45 min then at RT for 40min. The RM is quenched with sat. aq. NH4CI and extracted with EtOAc. The organic layer is washed twice with brine, dried over MgSC>4, filtered and concentrated. The residue is purified by FC (HepLEtOAc 9:1 to 8:2) to afford the expected product as a white solid (42 mg, 23%). LC-MS A: t _R = 0.86 min; [M+H] ⁺ = 318.14.

C.1.39.1. 5-(4-Bromo-2-methoxy phenyl)isoxazol-3-ol

HCI cone. (6.8 mL) is added dropwise at RT to a stirred suspension of 3-(4-bromo-2-methoxyphenyl)-3- oxo-N-((tetrahydro-2H-pyran-2-yl)oxy)propanamide (284 mg, 0.763 mmol) in MeOH (1.7 mL). The RM is stirred at RT for 30 min. Water (4 mL) is added and the precipitate is filtered off, washing with 1.2 mL water to afford the expected product as a white solid (169 mg, 82%) LC-MS A: t _R = 0.79 min, [M+H] ⁺ = 271.99.

C.1.39.2. 3-(4-Bromo-2-methoxyphenyl)-3-oxo-N-((tetrahydro-2H-pyran-2- yl)oxy)propanamide

To a solution of ethyl 3-(4-bromo-2-methoxyphenyl)-3-oxopropanoate (971 mg, 1.33 mmol) in NMP (15.7 mL) are sequentially added 0-(tetrahydro-2H-pyran-2-yl)hydroxylamine (512 mg, 4.19 mmol) and DMAP (433 mg, 3.55 mmol) at RT. The RM is heated to 115°C and stirred overnight, then cooled to RT. The mixture is partitioned between 40 mL HCI 0.5M (pH 2) and 40 mL EtOAc. The organic layer is washed three times with 40 mL NaCI sat. The aqueous layer is reextracted with 40 mL EtOAc. The organic layers are combined, dried over MgSC>4, filtered and concentrated. The residue is purified by FC (HepLEtOAc), affording the title compound as a white solid (301 mg, 25%). LC-MS A: t _R = 0.76 min, [M+H] ⁺ = 373.98.

C.1.39.3. Ethyl 3-(4-bromo-2-methoxyphenyl)-3-oxopropanoate

1-(4-bromo-2-methoxyphenyl)ethanone (1.00 g, 4.37 mmol) is dissolved in diethyl carbonate (5.6 mL, 46.2 mmol). NaH (66% suspension in oil, 384 mg, 9.6 mmol) is added carefully. The RM is stirred overnight at RT. Water is added carefully and the mixture is extracted two times with EtOAc. The organic layers are washed with water, brine, dried over MgSC>4, filtered and concentrated. The residue is purified by FC (Hept-EtOAc, affording the title compound as a light yellow oil (933mg, 71 %). LC-MS A: t _R = 0.87min, [M+H] ⁺ = 303.01.

C.1.40. 5-(2-ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henyl)isoxazol-3-ol

Butyllithium solution 2.5M (2 mL, 5.03 mmol) is added dropwise, at -78 °C under nitrogen, to a stirred solution of 5- (4-bromo-2-ethoxyphenyl)isoxazol-3-ol (286 mg, 1.01 mmol) and 2-isopropoxy-4,4,5,5-tetramethyl-1 ,3,2- dioxaborolane (0.733 mL, 3.52 mmol) in dry THF (15 mL). The RM is stirred at -78 °C for 15 min then water is added at -78°C and mixture is left stirring at RT for 40 min. A saturated solution of NH4CI is added and the aqueous phase is extracted with EtOAc. The organic layer is washed twice with brine, then it is dried over MgS04, filtered and concentrated. The crude residue is purified by FC (Hept to Hept EtOAc 1 :1 ), to afford the title compound as a white solid (390 mg, quant.). LC-MS B: t _R = 0.98 min; [M+H] ⁺ = 332.34 & [M+H+MeCN] ⁺ = 373.55 .

C.1.40.1. 5-(4-bromo-2-ethoxy pheny l)isoxazol-3-ol

To a solution of ethyl 3-(4-bromo-2-ethoxyphenyl)propiolate (1017 mg, 3.42 mmol) in EtOH (30 mL), Hydroxylamine hydrochloride (721 mg, 10.3 mmol) is added followed by dropwise addition of NaOH 10% (6.85 mL, 18.8 mmol); the RM is stirred overnight at RT. The solvent is distilled off under reduced pressure, the residue obtained is suspended in water, and the suspension is adjusted to pH 2-3 with a 2N aqueous HCI solution. The resultant solid is filtered off to afford the title compound as a white solid (380 mg, 39%). LC-MS B: tR = 0.91 min; [M+H] ⁺ = 284.17/286.25 .

C.1.40.2. Ethyl 3-(4-bromo-2-ethoxyphenyl)propiolate A C02 (gas) inlet is set up in the reaction apparatus and CO2 is bubbled continuously into a stirred solution of ((4-bromo-2-ethoxyphenyl)ethynyl)trimethylsilane (1950 mg, 6.56 mmol) in DMSO (20 mL). Cesium fluoride (1220 mg, 7.87 mmol) is added and the RM is stirred at RT for 2 h. CO2 bubbling is stopped and iodoethane (0.639 mL, 7.87 mmol) is added dropwise. The RM is further stirred at RT for 3 h and then poured into water. The aqueous phase is extracted twice with EtOAc and the combined organic layers are washed back with water and finally brine. The organic phase is dried over MgSC>4 and concentrated to dryness. Purification by FC (HepLEtOAc 100:0 to 85:15) yields the tile compound as an orange oil (1.017 g, 52%). LC-MS B: t _R = 1.08 min; [M+H] ⁺ = 297.20/299.23 .

C.1.40.3. ((4-Bromo-2-ethoxyphenyl)ethynyl)trimethylsilane

To a solution of 4-bromo-2-ethoxy-1-iodobenzene (2120 mg, 6.48 mmol) in THF (20 mL) are added TEA

(2.71 mL, 19.5 mmol), ethynyltrimethylsilane (1.12 mL, 7.78 mmol) and copper iodide (61.7 mg, 0.324 mmol). The RM is degassed and put under argon 3 times. Then trans- dichlorobis(triphenylphosphine)palladium(ll) (91 mg, 0.13 mmol) is added and the RM is degassed a last time, put under argon and stirred at 70°C for 16 h. The mixture is cooled to RT and partitioned between EtOAc and water. The organic layer is washed with brine, dried over Na2SC>4, filtered and the solvent is evaporated. The resulting residue is purified by FC (HepLEtOAc 100:0 to 90:10) to yield the title compound as an orange oil (1.95 g, 100%). LC-MS B: t _R = 1.18 min; no ionization; ¹ H NMR (400 MHz, d6-DMSO) δ: 7.31 (d, J = 8.2 Hz, 1 H), 7.24 (d, J = 1.6 Hz, 1 H), 7.10 (dd, Ji = 1.7 Hz, J ₂ = 8.1 Hz, 1 H), 4.09 (q, J = 7.0 Hz, 2 H), 1.33 (t, J = 6.8 Hz, 3 H), 0.22 (s, 9 H).

C.1.41. Methyl 2-(4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-2-(trifluoromethoxy)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-(trifluoromethoxy)phenyl)acetate (1.896 g, 5.58 mmol) in anh. DMF (25 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.432 g, 5.58 mmol), potassium acetate (2.192 g, 22.30 mmol) and Pd(dppf)CI ₂ (454 mg, 0.61 mmol). The RM is heated to 95°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with Et20. The filtrate is washed with water and the aqueous layer is extracted twice with Et20. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-2- (trifluoromethoxy)phenyl)acetate as a green oil (1.574 g, 78%). LC-MS B: t _R = 1.09 min; [M+H] ⁺ = 361.13.

C.1.41.1. Methyl 2-(4-bromo-2-(trifluoromethoxy)phenyl)acetate

To a solution of 2-(4-bromo-2-(trifluoromethoxy)phenyl)acetic acid (2.000 g, 6.56 mmol) in anh. DMF (30 mL) at RT are added cesium carbonate (4.277 g, 13.10 mmol) and iodomethane (0.82 mL, 13.10 mmol) and the RM is stirred at RT, under nitrogen, for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-(trifluoromethoxy)phenyl)acetate as a clear oil (1.896 g, 92%). LC-MS B: t _R = 1.01 min; no ionization.

C.1.42. Methyl 2-(2-cyclopropoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-cyclopropoxyphenyl)acetate (2.009 g, 7.05 mmol) in anh. 1 ,4-dioxane (30 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.807 g, 7.05 mmol), potassium acetate (2.766 g, 28.20 mmol) and Pd(dppf)CI ₂ (573 mg, 0.77 mmol). The RM is heated to 95°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then dried over MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(2-cyclopropoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a yellow oil (1.912 g, 82%). LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 333.25.

C.1.42.1. Methyl 2-(4-bromo-2-cyclopropoxyphenyl)acetate

A cooled (0°C) solution of diethylzinc (1 M in hexanes, 32.6 mL, 32.6 mmol) in anh. DCM (30 mL) is treated dropwise with trifluoroacetic acid (1.72 mL, 22.30 mmol) and the mixture is stirred at 0°C, under nitrogen, for 10 min. Diiodomethane (5.35 mL, 65.20 mmol) is then added dropwise to the cooled mixture and stirring at

0°C is continued for 10 min. A solution of methyl 2-(4-bromo-2-(vinyloxy)phenyl)acetate (2.396 g, 8.57 mmol) in anh. DCM (40 mL) is then added dropwise and the resulting mixture is further stirred at 0°C for 30 min, and then at RT for 5h. The RM is then treated with aq. sat. NH4CI and the layers are separated. The aqueous layer is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords methyl 2-(4-bromo-2-cyclopropoxyphenyl)acetate as a light yellow oil (2.009 g, 82%). LC-MS B: t _R = 0.99 min; no ionization.

C.1.42.2. Methyl 2-(4-bromo-2-(vinyloxy)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-hydroxyphenyl)acetate (3.160 g, 12.90 mmol) in anh. toluene (35 mL) at RT are added successively sodium carbonate (820 mg, 7.74 mmol) and bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (89.3 mg, 0.129 mmol), and the mixture is degassed with nitrogen. Vinyl acetate (2.4 mL, 25.80 mmol) is then added and the resulting mixture is heated to 100°C, under nitrogen, for 5h. The RM is allowed to cool to RT and water is added. The mixture is extracted three times with EtOAc and the combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-

(vinyloxy)phenyl)acetate as a yellow oil (2.253 g, 64%). LC-MS B: t _R = 0.96 min; no ionization.

C.1.42.3. Methyl 2-(4-bromo-2-hydroxyphenyl)acetate

A solution of 2-(4-bromo-2-hydroxyphenyl)acetic acid (3.000 g, 12.30 mmol) in anh. MeOH (45 mL) is treated dropwise with a solution of concentrated HCI (12 M, 1.02 mL, 12.30 mmol) in anh. MeOH (15 mL) and the resulting solution is heated to 70°C, under nitrogen, for 2h. The RM is then allowed to cool to RT and methanol is removed under reduced pressure. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-hydroxyphenyl)acetate as a colorless solid (2.733 g, 90%). LC-MS B: t _R = 0.80 min; no ionization.

C.1.43. Isopropyl 2-(2-isopropoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2- yl)phenyl)acetate

Bis(pinacolato)diboron (1618 mg, 6.31 mmol) followed by potassium acetate (2477 mg, 25.2 mmol) are added to a RT solution of isopropyl 2-(4-bromo-2-isopropoxyphenyl)acetate (2046 mg, 6.31 mmol) in DMF (25 mL). The RM is purged with N2 and dichloro(1 ,1'-bis(diphenylphosphino)ferrocene) palladium (II) (513 mg, 0.694 mmol) is added. The RM is heated at 95°C overnight, then cooled to RT, filtered over a pad of celite and rinsed with EbO. Water and Et20 are added, and the two layers are separated. The aqueous layer is extracted with Et20 (3x). The combined organic layers are washed with water (2x), brine, dried over MgSC>4, filtered and evaporated in vacuum. The residue is purified by FC (Hept:EtOAc 100:0 to 70:30) to afford the title compound as a light green oil (1.604 g, 70%). LC- MS B: t _R = 1.14 min; [M+H] ⁺ = 363.25.

C.1.43.1. Isopropyl 2-(4-bromo-2-isopropoxyphenyl)acetate

To 4-bromo-2-hydroxyphenylacetic acid (2000 mg, 8.22 mmol) in DMF (25 mL) is added cesium carbonate (5359 mg, 16.4 mmol) and 2-bromopropane (2.73 mL, 28.8 mmol) at 0°C. The RM is warmed up to RT and stirred for 1 h, then heated to 45°C and stirred for 24h. Water is added and the resulting mixture is extracted with Et20 (3x). Organic layers are mixed and washed with additional water (2x), brine, then dried over a phase separator and concentrated under vacuum. The residue is purified by FC (HeptEtOAc 100:0 to 75:25) to yield the title compound as a light green oil (2.046 g, 79%). LC-MS B: t _R = 1.10 min; [M+H] ⁺ = 315.11.

C.1.44. Methyl 2-(2-ethoxy-6-fluoro-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetate (1.370 g, 4.71 mmol) in anh. DMF (12 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.207 g, 4.71 mmol), potassium acetate (1.847 g, 18.80 mmol) and Pd(dppf)CI ₂ (383 mg, 0.51 mmol). The RM is heated to 90°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(2-ethoxy-6-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a colorless solid (0.970 g, 61 %). LC-MS B: t _R = 1.09 min; [M+H] ⁺ = 339.21.

C.1.44.1. Methyl 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetate

To a solution of 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetic acid (1.440 g, 5.20 mmol) in anh. DMF (15 mL) at RT are added cesium carbonate (2.1 17 g, 6.50 mmol) and iodomethane (0.48 mL, 7.80 mmol) and the RM is stirred at RT, under nitrogen, for 15 min. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetate as a colorless oil (1.370 g, 91 %). LC-MS B: t _R = 1.01 min; [M+H] ⁺ = 290.99.

C.1.44.2. 2-(4-Bromo-2-ethoxy-6-fluorophenyl)acetic acid

A mixture of 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetonitrile (1.440 g, 5.58 mmol), water (5 mL), 95% sulfuric acid (6 mL) and acetic acid (7 mL) is heated to 1 10°C, under nitrogen, for 3h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetic acid as a colorless solid (1.440 g, 93%). LC-MS B: t _R = 0.88 min; no ionization.

C.1.44.3. 2-(4-Bromo-2-ethoxy-6-fluorophenyl)acetonitrile

A solution of 5-bromo-2-(chloromethyl)-1 -ethoxy-3-fluorobenzene (2.860 g, 10.10 mmol) in MeCN (27 mL) and water (3.5 mL) is treated with sodium cyanide (669 mg, 13.10 mmol) and the RM is heated to 80°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the mixture is extracted twice with DCM. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords 2-(4-bromo-2-ethoxy-6-fluorophenyl)acetonitrile as a colorless solid (1.440 g, 55%). LC-MS B: t _R = 0.97 min; no ionization.

C.1.44.4. 5-Bromo-2-(chloromethyl)-1-ethoxy-3-fluorobenzene

A cooled (0°C) mixture of (4-bromo-2-ethoxy-6-fluorophenyl)methanol (2.180 g, 8.75 mmol) and zinc chloride (29.8 mg, 0.219 mmol) in anh. DCM (17 mL) is treated dropwise with thionyl chloride (1.28 mL, 17.50 mmol) and the RM is stirred at 0°C for 2h. The RM is concentrated under reduced pressure affording crude 5-bromo- 2-(chloromethyl)-1 -ethoxy-3-fluorobenzene as a pale pink oil (2.330 g, 99%). LC-MS B: t _R = 1.07 min; no ionization.

C.1.44.5. (4-Bromo-2-ethoxy-6-fluorophenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-ethoxy-6-fluorobenzoate (3.150 g, 1 1.40 mmol) in anh. THF (30 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 34.1 mL, 34.1 mmol). The mixture is further stirred at -78°C, under nitrogen, for 15 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 45 min, and the cooled RM is then treated successively with water (35 mL) and

2.8 N aq. NaOH (25 mL). The mixture is allowed to warm-up to RT and is further stirred for 30 min. The resulting mixture is filtered over celite, washing with THF. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to EtOAc) affords (4-bromo-2-ethoxy-6-fluorophenyl)methanol as a colorless solid (2.680 g, 95%). LC-MS B: t _R = 0.84 min; no ionization.

C.1.44.6. Methyl 4-bromo-2-ethoxy-6-fluorobenzoate

To a solution of methyl 4-bromo-2-fluoro-6-hydroxybenzoate (2.930 g, 11.20 mmol) in anh. DMF (14 mL) at RT are added successively cesium carbonate (3.642 g, 1 1.20 mmol) and iodoethane (0.90 mL, 11.20 mmol) and the RM is stirred at RT for 30 min. Additional cesium carbonate (3.729 g, 1 1.40 mmol) and iodoethane (0.92 mL, 1 1.40 mmol) are then added and the RM is stirred at RT for 20 min. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 4-bromo-2-ethoxy-6-fluorobenzoate as a yellow oil

(3.150 g, quantitative). LC-MS B: t _R = 0.97 min; [M+H] ⁺ = 277.08.

C.1.45. Methyl 2-(2-isobutyl-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-isobutylphenyl)acetate (2.271 g, 7.13 mmol) in anh. DMF (25 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.828 g, 7.13 mmol), potassium acetate (2.798 g, 28.50 mmol) and Pd(dppf)CI ₂ (579 mg, 0.78 mmol). The RM is heated to 95°C, under nitrogen, for 16h. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(2-isobutyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate as a yellow oil (1.822 g, 77%). LC-MS B: t _R = 1.13 min; [M+H] ⁺ = 333.24.

C.1.45.1. Methyl 2-(4-bromo-2-isobutylphenyl)acetate

To a solution of 2-(4-bromo-2-isobutylphenyl)acetic acid (2.457 g, 8.64 mmol) in anh. DMF (30 mL) at RT are added cesium carbonate (5.633 g, 17.30 mmol) and iodomethane (1.09 mL, 17.30 mmol) and the RM is stirred at RT, under nitrogen, for 1 h. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-isobutylphenyl)acetate as a clear oil (2.271 g, 92%). LC-MS B: t _R = 1.06 min; no ionization.

C.1.45.2. 2-(4-Bromo-2-isobutylphenyl)acetic acid

A mixture of 2-(4-bromo-2-isobutylphenyl)acetonitrile (2.162 g, 8.41 mmol), water (8 mL), 95% sulfuric acid (9 mL) and acetic acid (6 mL) is heated to 1 10°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-isobutylphenyl)acetic acid as an amber oil (2.457 g, quantitative). LC-MS B: t _R = 0.96 min; no ionization. C.1.45.3. 2-(4-Bromo-2-isobutylphenyl)acetonitrile

A solution of 4-bromo-1 -(chloromethyl)-2-isobutylbenzene (2.381 g, 9.00 mmol) in MeCN (24 mL) and water (3 mL) is treated with sodium cyanide (597 mg, 1 1.70 mmol) and the RM is heated to 80°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the RM is extracted twice with DCM. The combined organic layers are dried over anh.

MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords 2-(4-bromo-2-isobutylphenyl)acetonitrile as a clear oil (2.162 g, 95%). LC-MS B: t _R = 1.05 min; no ionization.

C.1.45.4. 4-Bromo-1 -(chloromethyl)-2-isobuty I benzene

A cooled (0°C) mixture of (4-bromo-2-isobutylphenyl)methanol (2.192 g, 8.83 mmol) and zinc chloride (30.1 mg, 0.221 mmol) in anh. DCM (20 mL) is treated dropwise with thionyl chloride (1.29 mL, 17.70 mmol) and the RM is stirred at 0°C for 4h. The RM is concentrated under reduced pressure affording crude 4-bromo-1 - (chloromethyl)-2-isobutylbenzene as a light pink oil (2.381 g, quantitative). LC-MS B: tR = 1.13 min; no ionization.

C.1.45.5. (4-Bromo-2-isobutylphenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-isobutylbenzoate (2.712 g, 9.71 mmol) in anh. THF (60 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 29.1 mL, 29.1 mmol). The mixture is further stirred at -78°C, under nitrogen, for 15 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 30 min, and the cooled RM is treated successively with water (1 mL), 2.8 N aq. NaOH (1 mL) and water (3 mL). The mixture is then allowed to warm-up to RT and is further stirred for 30 min. The resulting mixture is filtered over celite, washing with THF and the filtrate is concentrated to dryness under reduced pressure. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (4-bromo-2- isobutylphenyl)methanol (2.192 g, 93%). LC-MS B: t _R = 0.96 min; no ionization.

C.1.45.6. Methyl 4-bromo-2-isobutylbenzoate

To a solution of 4-bromo-2-isobutylbenzoic acid (4.254 g, 14.30 mmol) in anh. DMF (50 mL) at RT are added successively cesium carbonate (9.304 g, 28.60 mmol) and iodomethane (1.80 mL, 28.60 mmol) and the RM is stirred at RT for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 4-bromo-2-isobutylbenzoate as a light yellow oil (3.462 g, 89%). LC-MS B: t _R = 1.11 min; no ionization.

C.1.45.7. 4-Bromo-2-isobutylbenzoic acid

To a cooled (0°C) solution of 4-bromo-2-fluorobenzoic acid (5.000 g, 22.40 mmol) in anh. THF (40 mL) is added dropwise a solution of isobutylmagnesium bromide (2.0 M in Et20, 33.5 mL, 67.0 mmol) and the RM is further stirred at RT, under nitrogen, overnight. MeOH (10 mL) is then added dropwise to the cooled (0°C) reaction mixture that is further stirred at 0°C for 5 min. The resulting mixture is then concentrated to dryness under reduced pressure and the residue is partitioned between EtOAc and 2 M aq. HCI. The layers are separated, and the aq. layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords 4-bromo-2-isobutylbenzoic acid as a light yellow solid (4.254 g, 74%). LC-MS B: t _R = 0.97 min; no ionization.

C.1.46. Methyl 2-(2-ethyl-6-methyl-4-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-ethyl-6-methylphenyl)acetate (1.176 g, 4.34 mmol) in anh. DMF (15 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.1 12 g, 4.34 mmol), potassium acetate (1.703 g, 17.30 mmol) and Pd(dppf)CI ₂ (353 mg, 0.47 mmol). The RM is heated to 90°C, under nitrogen, for 16h. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(2-ethyl-6-methyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a light green oil (895 mg, 65%). LC-MS B: t _R = 1.08 min; [M+H] ⁺ = 319.28.

C.1.46.1. Methyl 2-(4-bromo-2-ethyl-6-methy Ipheny l)acetate

To a solution of 2-(4-bromo-2-ethyl-6-methylphenyl)acetic acid (2.993 g, 1 1.60 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (7.585 g, 23.30 mmol) and iodomethane (1.46 mL, 23.30 mmol) and the RM is stirred at RT, under nitrogen, for 5h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(4-bromo-2-ethyl-6-methylphenyl)acetate as a yellow oil (1.176 g, 37%). LC-MS B: t _R = 1.03 min; no ionization.

C.1.46.2. 2-(4-Bromo-2-ethyl-6-methylphenyl)acetic acid

A mixture of 2-(4-bromo-2-ethyl-6-methylphenyl)acetonitrile (2.477 g, 10.40 mmol), water (10 mL), 95% sulfuric acid (11 mL) and acetic acid (7.5 mL) is heated to 1 10°C, under nitrogen, for 1.5h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgS0 ₄ , filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-ethyl-6-methylphenyl)acetic acid as an off-white solid (2.993 g, quantitative). LC-MS B: t _R = 0.81 min; no ionization.

C.1.46.3. 2-(4-Bromo-2-ethyl-6-methylphenyl)acetonitrile

A solution of 5-bromo-2-(chloromethyl)-1 -ethyl-3-methylbenzene (2.849 g, 11.50 mmol) in MeCN (30 mL) and water (3.7 mL) is treated with sodium cyanide (764 mg, 15.00 mmol) and the RM is heated to 80°C, under nitrogen, for 1 h. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the RM is extracted twice with DCM. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords 2-(4-bromo-2-ethyl-6-methylphenyl)acetonitrile as a clear oil (2.477 g, 90%). LC-MS B: t _R = 0.99 min; no ionization.

C.1.46.4. 5-Bromo-2-(chloromethyl)-1-ethyl-3-methylbenzene

A cooled (0°C) mixture of (4-bromo-2-ethyl-6-methylphenyl)methanol (2.525 g, 1 1.00 mmol) and zinc chloride (37.6 mg, 0.276 mmol) in anh. DCM (30 mL) is treated dropwise with thionyl chloride (1.61 mL, 22.00 mmol) and the RM is stirred at 0°C for 1 h. The RM is concentrated under reduced pressure affording crude 5-bromo- 2-(chloromethyl)-1-ethyl-3-methylbenzene as a light brown oil (2.849 g, quantitative). LC-MS B: t _R = 1.08 min; no ionization.

C.1.46.5. (4-Bromo-2-ethyl-6-methylphenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-ethyl-6-methylbenzoate (3.355 g, 13.00 mmol) in anh. THF (60 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 39.0 mL, 39.0 mmol). The mixture is further stirred at -78°C, under nitrogen, for 15 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 1 h, and the cooled RM is treated successively with water (1 mL), 2.8 N aq.

NaOH (1 mL) and water (3 mL). The mixture is then allowed to warm-up to RT and is further stirred for 30 min. The resulting mixture is filtered over celite, washing with THF and the filtrate is concentrated to dryness under reduced pressure. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (4- bromo-2-ethyl-6-methylphenyl)methanol (2.525 g, 84%). LC-MS B: t _R = 0.87 min; no ionization.

C.1.46.6. Methyl 4-bromo-2-ethyl-6-methylbenzoate

To a solution of 4-bromo-2-ethyl-6-methylbenzoic acid (3.465 g, 14.30 mmol) in anh. DMF (35 mL) at RT are added cesium carbonate (9.288 g, 28.50 mmol) and iodomethane (1.79 mL, 28.50 mmol) and the RM is stirred at RT for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords methyl 4-bromo-2-ethyl-6-methylbenzoate as a clear oil (3.355 g, 92%). LC-MS B: t _R = 1.02 min; no ionization.

C.1.46.7. 4-Bromo-2-ethyl-6-methy I benzoic acid

To a cooled (0°C) solution of 4-bromo-2-fluoro-6-methylbenzoic acid (4.000 g, 16.30 mmol) in anh. THF (40 mL) is added dropwise a solution of ethylmagnesium bromide (1.0 M in THF, 49.0 mL, 49.0 mmol) and the RM is further stirred at RT, under nitrogen, overnight. MeOH (15 mL) is then added dropwise to the cooled (0°C) reaction mixture that is further stirred at 0°C for 5 min. The resulting mixture is then concentrated to dryness under reduced pressure and the residue is partitioned between EtOAc and 2 M aq. HCI. The layers are separated, and the aq. layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords 4-bromo-2-ethyl-6-methylbenzoic acid as a colorless solid (3.465 g, 87%). LC-MS B: t _R = 0.86 min; no ionization.

C.1.47. Methyl 2-(2-propyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henyl)acetate

To a solution of methyl 2-(4-bromo-2-propylphenyl)acetate (2.380 g, 8.78 mmol) in anh. DMF (20 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (2.251 g, 8.78 mmol), potassium acetate (3.446 g, 35.10 mmol) and Pd(dppf)CI ₂ (714 mg, 0.96 mmol). The RM is heated to 90°C, under nitrogen, for 16h. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(2-propyl -(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate as a colorless oil (2.230 g, 80%). LC-MS B: t _R = 1.10 min; [M+H] ⁺ = 319.31.

C.1.47.1. Methyl 2-(4-bromo-2-propylphenyl)acetate

To a solution of 2-(4-bromo-2-propylphenyl)acetic acid (2.770 g, 10.80 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (5.265 g, 16.20 mmol) and iodomethane (1.02 mL, 16.20 mmol) and the RM is stirred at RT, under nitrogen, for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-propylphenyl)acetate as a yellow oil (2.380 g, 81 %). LC-MS B: t _R = 1.04 min; no ionization.

C.1.47.2. 2-(4-Bromo-2-propylphenyl)acetic acid

A mixture of 2-(4-bromo-2-propylphenyl)acetonitrile (2.570 g, 10.80 mmol), water (10 mL), 95% sulfuric acid (1 1.5 mL) and acetic acid (8 mL) is heated to 1 10°C, under nitrogen, for 3h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-propylphenyl)acetic acid as a pale grey solid (3.390 g, quantitative). LC-MS B: t _R = 0.91 min; no ionization.

C.1.47.3. 2-(4-Bromo-2-propylphenyl)acetonitrile

A solution of 4-bromo-1 -(chloromethyl)-2-propylbenzene (2.980 g, 12.00 mmol) in MeCN (32 mL) and water (3.9 mL) is treated with sodium cyanide (767 mg, 15.60 mmol) and the RM is heated to 80°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the RM is extracted twice with DCM. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to EtOAc) affords 2-(4-bromo-2-propylphenyl)acetonitrile as a pale yellow oil (2.570 g, 90%). LC-MS B: t _R = 1.02 min; no ionization. C.1.47.4. 4-Bromo-1 -(chloromethyl)-2-propyl benzene

A cooled (0°C) mixture of (4-bromo-2-propylphenyl)methanol (2.650 g, 11.60 mmol) and zinc chloride (39.4 mg, 0.289 mmol) in anh. DCM (23 mL) is treated dropwise with thionyl chloride (1.69 mL, 23.10 mmol) and the RM is stirred at 0°C for 3h, and then at RT overnight. The RM is concentrated under reduced pressure affording crude 4-bromo-1 -(chloromethyl)-2-propylbenzene as a grey oil (2.98 g, quantitative). LC-MS B: tR =

1.10 min; no ionization.

C.1.47.5. (4-Bromo-2-propylphenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-propylbenzoate (3.300 g, 12.80 mmol) in anh. THF (60 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 38.5 mL, 38.5 mmol). The mixture is further stirred at -78°C, under nitrogen, for 15 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 45 min, and the cooled RM is treated successively with water (1.5 mL), 2.8 N aq. NaOH (1.5 mL) and water (4 mL). The mixture is then allowed to warm-up to RT and stirring was continued for 30 min. The resulting mixture was filtered over celite washing with THF and the filtrate was concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (4-bromo-2- propylphenyl)methanol as a colorless oil (2.650 g, 90%). LC-MS B: t _R = 0.91 min; no ionization.

C.1.47.6. Methyl 4-bromo-2-propylbenzoate

To a solution of 4-bromo-2-propylbenzoic acid (3.590 g, 14.80 mmol) in anh. DMF (30 mL) at RT are added successively cesium carbonate (9.623 g, 29.50 mmol) and iodomethane (1.86 mL, 29.50 mmol) and the RM is stirred at RT for 16h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 4-bromo-2-propylbenzoate as a colorless oil (3.300 g, 87%). LC-MS B: tR = 1.05 min; no ionization.

C.1.47.7. 4-Bromo-2-propy I benzoic acid

To a cooled (0°C) solution of 4-bromo-2-fluorobenzoic acid (5.000 g, 22.40 mmol) in anh. THF (40 mL) is added dropwise a solution of propylmagnesium bromide (2.0 M in THF, 33.50 mL, 67.00 mmol) and the RM is further stirred at RT, under nitrogen, overnight. MeOH (10 mL) is then added dropwise to the cooled (0°C) reaction mixture that is further stirred at 0°C for 5 min. The resulting mixture is then concentrated to dryness under reduced pressure and the residue is partitioned between EtOAc and 2 M aq. HCI. The layers are separated, and the aq. layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/2) affords 4-bromo-2-propylbenzoic acid as a colorless solid (3.590 g, 66%). LC-MS B: t _R = 0.93 min; no ionization. C.1.48. Methyl 2-(2-ethyl-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-ethylphenyl)acetate (900 mg, 3.24 mmol) in anh. DMF (15 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (832 mg, 3.24 mmol), potassium acetate (1.274 g, 13.00 mmol) and Pd(dppf)CI ₂ (264 mg, 0.35 mmol). The RM is heated to 90°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords methyl 2-(2-ethyl -(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate as a light yellow oil (708 mg, 72%). LC-MS B: t _R = 1.05 min; [M+H] ⁺ = 305.22.

C.1.48.1. Methyl 2-(4-bromo-2-ethylphenyl)acetate

To a solution of 2-(4-bromo-2-ethylphenyl)acetic acid (2.1 18 g, 8.05 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (5.246 g, 16.10 mmol) and iodomethane (1.01 mL, 16.10 mmol) and the RM is stirred at RT, under nitrogen, for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(4-bromo-2-ethylphenyl)acetate as a light yellow oil (2.043 g, 99%). LC-MS B: t _R = 0.99 min; no ionization.

C.1.48.2. 2-(4-Bromo-2-ethylphenyl)acetic acid

A mixture of 2-(4-bromo-2-ethylphenyl)acetonitrile (1.859 g, 7.99 mmol), water (7.5 mL), 95% sulfuric acid (8.3 mL) and acetic acid (5.8 mL) is heated to 1 10°C, under nitrogen, for 4h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-ethylphenyl)acetic acid as an amber solid (2.118 g, quantitative). LC-MS B: tR = 0.85 min; no ionization.

C.1.48.3. 2-(4-Bromo-2-ethylphenyl)acetonitrile

A solution of 4-bromo-1-(chloromethyl)-2-ethylbenzene (2.050 g, 8.34 mmol) in MeCN (24 mL) and water (3 mL) is treated with sodium cyanide (553 mg, 10.80 mmol) and the RM is heated to 80°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the RM is extracted twice with DCM. The combined organic layers are dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc

= 7/3) affords 2-(4-bromo-2-ethylphenyl)acetonitrile as a colorless solid (1.859 g, 99%). LC-MS B: t _R = 0.95 min; no ionization.

C.1.48.4. 4-Bromo-1-(chloromethyl)-2-ethylbenzene

A cooled (0°C) mixture of (4-bromo-2-ethylphenyl)methanol (1.854 g, 8.30 mmol) and zinc chloride (28.3 mg, 0.208 mmol) in anh. DCM (20 mL) is treated dropwise with thionyl chloride (1.21 mL, 16.60 mmol) and the RM is stirred at 0°C for 2h. The RM is concentrated under reduced pressure affording crude 4-bromo-1 - (chloromethyl)-2-ethylbenzene as a light purple oil (2.050 g, quantitative). LC-MS B: tR = 1.04 min; no ionization.

C.1.48.5. (4-Bromo-2-ethylphenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-ethylbenzoate (2.219 g, 9.01 mmol) in anh. THF (60 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 27.0 mL, 27.0 mmol). The mixture is further stirred at -78°C, under nitrogen, for 15 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 45 min, and the cooled RM is treated successively with water (1 mL), 2.8 N aq. NaOH (1 mL) and water (3 mL). The mixture is then allowed to warm-up to RT and is further stirred for 30 min. The resulting mixture is filtered over celite, washing with THF and the filtrate is concentrated to dryness under reduced pressure. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (4-bromo-2- ethylphenyl)methanol (1.854 g, 96%). LC-MS B: t _R = 0.84 min; no ionization.

C.1.48.6. Methyl 4-bromo-2-ethylbenzoate

To a solution of 4-bromo-2-ethylbenzoic acid (3.003 g, 12.80 mmol) in anh. DMF (30 mL) at RT are added cesium carbonate (8.355 g, 25.60 mmol) and iodomethane (1.61 mL, 25.60 mmol) and the RM is stirred at RT for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 4-bromo-2-ethylbenzoate as a clear oil (2.735 g, 88%). LC-MS B: t _R = 1.02 min; no ionization.

C.1.48.7. 4-Bromo-2-ethyl benzoic acid

To a cooled (0°C) solution of 4-bromo-2-fluorobenzoic acid (5.000 g, 22.40 mmol) in anh. THF (40 mL) is added dropwise a solution of ethylmagnesium bromide (1.0 M in THF, 67.1 mL, 67.1 mmol) and the RM is further stirred at RT, under nitrogen, for 3h. MeOH (15 mL) is then added dropwise to the cooled (0°C) reaction mixture that is further stirred at 0°C for 5 min. The resulting mixture is then concentrated to dryness under reduced pressure and the residue is partitioned between EtOAc and 2 M aq. HCI. The layers are separated, and the aq. layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords 4-bromo-2-ethylbenzoic acid as a colorless solid (3.003 g, 59%). LC-MS B: tR = 0.87 min; no ionization.

C.1.49. Methyl 2-(2-chloro-6-methyl-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-chloro-6-methylphenyl)acetate (2.614 g, 9.42 mmol) in anh. DMF (25 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (2.416 g, 9.42 mmol), potassium acetate (3.697 g, 37.70 mmol) and Pd(dppf)CI ₂ (766 mg, 1.04 mmol). The RM is heated to 90°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(2-chloro-6-methyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a light green oil (1.939 g, 63%). LC-MS B: t _R = 1.08 min; [M+H] ⁺ = 325.19.

C.1.49.1. Methyl 2-(4-bromo-2-chloro-6-methylphenyl)acetate

To a solution of 2-(4-bromo-2-chloro-6-methylphenyl)acetic acid (2.648 g, 10.00 mmol) in anh. DMF (25 mL) at RT are added cesium carbonate (6.548 g, 20.10 mmol) and iodomethane (1.26 mL, 20.10 mmol) and the RM is stirred at RT, under nitrogen, for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(4-bromo-2-chloro-6-methylphenyl)acetate as a clear oil (2.614 g, 94%). LC-MS B: t _R = 1.00 min; no ionization.

C.1.49.2. 2-(4-Bromo-2-chloro-6-methylphenyl)acetic acid

A mixture of 2-(4-bromo-2-chloro-6-methylphenyl)acetonitrile (2.504 g, 10.20 mmol), water (9 mL), 95% sulfuric acid (11 mL) and acetic acid (7 mL) is heated to 110°C, under nitrogen, for 4h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgS04, filtered and concentrated under reduced pressure affording crude 2-(4-bromo-2-chloro-6-methylphenyl)acetic acid as an off-white solid (2.648 g, 98%). LC-MS B: tR = 0.86 min; no ionization.

C.1.49.3. 2-(4-Bromo-2-chloro-6-methylphenyl)acetonitrile

A solution of 5-bromo-1 -chloro-2-(chloromethyl)-3-methylbenzene (2.752 g, 10.80 mmol) in MeCN (30 mL) and water (4 mL) is treated with sodium cyanide (719 mg, 14.10 mmol) and the RM is heated to 80°C, under nitrogen, for 1 h. The RM is then allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the mixture is extracted twice with DCM. The combined organic layers are dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords 2-(4-bromo-2-chloro-6-methylphenyl)acetonitrile as a colorless solid (2.504 g, 94%). LC-MS B: t _R = 0.96 min; no ionization.

C.1.49.4. 5-Bromo-1-chloro-2-(chloromethyl)-3-methylbenzene

A cooled (0°C) mixture of (4-bromo-2-chloro-6-methylphenyl)methanol (2.529 g, 10.70 mmol) and zinc chloride (36.6 mg, 0.268 mmol) in anh. DCM (30 mL) is treated dropwise with thionyl chloride (1.57 mL, 21.50 mmol) and the RM is stirred at 0°C for 4h. The RM is concentrated under reduced pressure affording crude 5-bromo-1 -chloro-2-(chloromethyl)-3-methylbenzene as a dark pink solid (2.752 g, quantitative). LC-MS B: tR = 1.05 min; no ionization. C.1.49.5. (4-Bromo-2-chloro-6-methylphenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-chloro-6-methylbenzoate (3.450 g, 12.60 mmol) in anh. THF (60 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 38.0 mL, 38.0 mmol). The mixture is further stirred at -78°C, under nitrogen, for 30 min and is then allowed to warm-up to RT. Stirring at RT is continued for 1.5h, and the cooled RM is then treated successively with water (1 mL), 2.8 N aq. NaOH (1 mL) and water (3 mL). The mixture is allowed to warm-up to RT and is further stirred for 30 min. The resulting mixture is filtered over celite, washing with THF and the filtrate is concentrated to dryness under reduced pressure. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords pure (4-bromo-2-chloro-

6-methylphenyl)methanol (2.529 g, 85%). LC-MS B: t _R = 0.90 min; no ionization.

C.1.49.6. Methyl 4-bromo-2-chloro-6-methylbenzoate

To a solution of 4-bromo-2-chloro-6-methylbenzoic acid (3.500 g, 13.30 mmol) in anh. DMF (35 mL) at RT are added successively cesium carbonate (8.685 g, 26.70 mmol) and iodomethane (1.68 mL, 26.70 mmol) and the RM is stirred at RT for 1 h. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 4-bromo-2-chloro-6-methylbenzoate as a dark orange oil (3.450 g, 98%). LC-MS B: t _R = 0.99 min; no ionization.

C.1.50. Methyl 3-ethoxy-5-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrrole-2-carboxylate

A mixture of methyl 3-ethoxy-1 H-pyrrole-2-carboxylate (265 mg, 1.57 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'- bi(1 ,3,2-dioxaborolane) (402 mg, 1.57 mmol), (1 ,5-cyclooctadiene)(methoxy)iridium(l) dimer (15.9 mg, 0.0235 mmol) and 4,4'-di-tert-butyl-2,2'-bipyridine (15 mg, 0.054 mmol) in THF (5 mL) is degassed with a nitrogen stream and then stirred at RT, under nitrogen, for 1 h. The RM is concentrated under reduced pressure and the residue is purified by FC (from heptane to heptane/EtOAc = 7/3) to afford methyl 3-ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)-1 H-pyrrole-2-carboxylate as a clear oil (490 mg, quantitative). LC-MS B: t _R = 0.88 min; [M+H] ⁺ = 296.25.

C.1.50.1. Methyl 3-ethoxy-1 H-pyrrole-2-carboxylate

To a solution of methyl 3-hydroxy-1 H-pyrrole-2-carboxylate (300 mg, 2.06 mmol) in anh. DMF (8 mL) at RT are added potassium carbonate (299 mg, 2.17 mmol) and iodoethane (0.174 mL, 2.17 mmol) and the RM is stirred at RT, under nitrogen, overnight. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to EtOAc) affords methyl 3-ethoxy-1 H-pyrrole-2-carboxylate as a light yellow solid (265 mg, 76%). LC-MS B: t _R = 0.60 min; [M+H] ⁺ = 170.09. C.1.51. Methyl 1-propyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrrole-2-carboxylate

To a solution of methyl 4-bromo-1 -propyl-1 H-pyrrole-2-carboxylate (1.721 g, 6.99 mmol) in anh. DMF (15 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.776 g, 6.99 mmol), potassium acetate (2.745 g, 28.00 mmol) and Pd(dppf)CI ₂ (512 mg, 0.69 mmol). The RM is heated to 90°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords methyl 1 -propyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H- pyrrole-2-carboxylate as a yellow oil (1.036 g, 51 %). LC-MS B: t _R = 1.02 min; [M+H] ⁺ = 294.33.

C.1.51.1. Methyl 4-bromo-1 -propyl-1 H-pyrrole-2-carboxylate

To a solution of methyl 4-bromo-1 H-pyrrole-2-carboxylate (1.500 g, 7.21 mmol) in anh. DMF (15 mL) at RT are added potassium carbonate (1.494 g, 10.80 mmol) and 1-iodopropane (0.84 mL, 8.65 mmol) and the RM is stirred at RT, under nitrogen, overnight. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 4-bromo-1 -propyl-1 H-pyrrole-2-carboxylate as a clear oil (1.721 g, 97%). LC-MS B: t _R = 0.99 min; no ionization.

C.1.52. Methyl 2-(3-ethyl-5-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acetate

A mixture of methyl 2-(3-ethylthiophen-2-yl)acetate (1.340 g, 7.27 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2- dioxaborolane) (1.1 19 g, 4.36 mmol), bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (50.4 mg, 0.0727 mmol) and 4,4'-di-tert-butyl-2,2'-bipyridine (47.8 mg, 0.175 mmol) in THF (35 mL) is degassed with a nitrogen stream and then stirred at 80°C, under nitrogen, overnight. The RM is concentrated under reduced pressure and the residue is purified by FC (from heptane to heptane/EtOAc = 4/1 ) to afford methyl 2-(3-ethyl-5-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)thiophen-2-yl)acetate as a pale yellow oil (1.781 g, 79%). LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 31 1.22.

C.1.52.1. Methyl 2-(3-ethylthiophen-2-yl)acetate

To a solution of 2-(3-ethylthiophen-2-yl)acetic acid (1.248 g, 7.33 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (3.581 g, 1 1.00 mmol) and iodomethane (0.55 mL, 8.79 mmol) and the RM is stirred at RT, under nitrogen, for 40 min. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(3-ethylthiophen-2-yl)acetate as a yellow oil (1.340 g, 99%). LC-MS B: t _R = 0.87 min; [M+H] ⁺ = 185.19. C.1.52.2. 2-(3-Ethylthiophen-2-yl)acetic acid

To a mixture of 2-(3-ethylthiophen-2-yl)acetonitrile (1.150 g, 7.60 mmol) in EtOH (6 mL) and water (6 mL) at RT is added potassium hydroxide (1.280 g, 22.80 mmol) and the RM is heated at reflux, under nitrogen, for 75 min. The RM is then allowed to cool to RT and ethanol is removed under reduced pressure. The resulting mixture is treated with 1 M aq. HCI and is extracted twice with DCM. The combined organic layers are dried over anh. MgSCX filtered and concentrated under reduced pressure affording crude 2-(3-ethylthiophen-2- yl)acetic acid as a yellow oil (1.247 g, 96%). LC-MS B: t _R = 0.72 min; [M+H] ⁺ = 170.94.

C.1.52.3. 2-(3-Ethylthiophen-2-yl)acetonitrile

A solution of 2-(chloromethyl)-3-ethylthiophene (506 mg, 3.15 mmol) in anhydrous DMSO (20 mL) is treated with sodium cyanide (617 mg, 12.60 mmol) and the RM is heated to 80°C, under nitrogen, for 40 min. The

RM is then allowed to cool to RT and is diluted with water. The resulting mixture is extracted three times with EtOAc and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords 2- (3-ethylthiophen-2-yl)acetonitrile as a yellow oil (360 mg, 76%). LC-MS B: t _R = 0.83 min; no ionization. C.1.52.4. 2-(Chloromethyl)-3-ethylthiophene

To a cooled (0°C) solution of (3-ethylthiophen-2-yl)methanol (500 mg, 3.52 mmol) in anh. DCM (18 mL) are added successively triethylamine (0.63 mL, 4.57 mmol) and 4-dimethylaminopyridine (43 mg, 0.35 mmol). Methanesulfonyl chloride (0.32 mL, 4.22 mmol) is then added dropwise and the resulting mixture is stirred at RT, under nitrogen, for 1 h. The RM is then diluted with water, the layers are separated and the aqueous layer is extracted twice with DCM. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure affording crude 2-(chloromethyl)-3-ethylthiophene as a yellow oil (505 mg, 90%). LC-MS B: t _R = 0.86 min; no ionization.

C.1.52.5. (3-Ethylthiophen-2-yl)methanol

To a cooled (-78°C) solution of methyl 3-ethylthiophene-2-carboxylate (2.270 g, 13.30 mmol) in anh. THF (80 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 40.0 mL, 40.0 mmol). The mixture is further stirred at -78°C, under nitrogen, for 10 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 30 min, and the cooled RM is then treated successively with water (1.5 mL), 15% aq. NaOH (1.5 mL) and water (4 mL). The mixture is allowed to warm-up to RT and is further stirred for 1 h. The resulting mixture is filtered over celite, washing with THF. EtOAc and water are added and the layers are separated. The aqueous layer is extracted twice with EtOAc and the combined organic layers are dried over anh. MgS04, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (3-ethylthiophen-2-yl)methanol as a colorless oil (2.030 g, quantitative). LC-MS B: [R = 0.66 min; no ionization. C.1.52.6. Methyl 3-ethylthiophene-2-carboxylate

To a solution of 3-ethylthiophene-2-carboxylic acid (3.130 g, 19.00 mmol) in anh. DMF (20 mL) at RT are added successively cesium carbonate (9.303 g, 28.60 mmol) and iodomethane (1.44 mL, 22.80 mmol) and the RM is stirred at RT for 1.5h. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure affording methyl 3-ethylthiophene-2-carboxylate as a yellow oil (3.340 g, quantitative). LC-MS B: t _R = 0.89 min; [M+H] ⁺ = 171.04.

C.1.53. Methyl 1-ethyl-4-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1 H-pyrrole-2-carboxylate

To a solution of methyl 4-bromo-1 -ethyl-1 H-pyrrole-2-carboxylate (1.567 g, 6.75 mmol) in anh. DMF (15 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.715 g, 6.75 mmol), potassium acetate (2.651 g, 27.00 mmol) and Pd(dppf)CI ₂ (494 mg, 0.67 mmol). The RM is heated to 90°C, under nitrogen, overnight. The RM is then allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are then washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords methyl 1-ethyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrrole- 2-carboxylate as a light yellow oil (841 mg, 45%). LC-MS B: t _R = 0.96 min; [M+H] ⁺ = 280.24.

C.1.53.1. Methyl 4-bromo-1 -ethyl-1 H-pyrrole-2-carboxylate

To a solution of methyl 4-bromo-1 H-pyrrole-2-carboxylate (1.500 g, 7.21 mmol) in anh. DMF (15 mL) at RT are added potassium carbonate (1.494 g, 10.80 mmol) and iodoethane (1.43 mL, 8.65 mmol) and the RM is stirred at RT, under nitrogen, for 2.5h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 4-bromo-1 -ethyl-1 H-pyrrole-2-carboxylate as a clear oil (1.567 g, 94%). LC-MS B: t _R = 0.94 min; no ionization.

C.1.54. Ethyl 2-methyl-5-(4,4,5 _! 5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1 H-pyrrole-3-carboxylate

To a microwave vial under nitrogen are added (1 ,5-cyclooctadiene)(methoxy)iridium(l) dimer (13 mg, 0.0192 mmol), 4,4'-di-tert-butyl-2,2'-dipyridyl (12.3 mg, 0.0448 mmol) and bis(pinacolato)diboron (164 mg, 0.64 mmol), followed by THF (2.5 mL), and 2-methyl-1 H-pyrrole-3-carboxylic acid ethyl ester (200 mg, 1.28 mmol). The microwave tube is sealed and the RM is stirred at RT for 3h, then at 80°C overnight. Bis(pinacolato)diboron (164 mg, 0.64 mmol) is added and the RM stirred at RT for 3h. After concentration under reduced pressure, the residue is purified by FC (HepLEtOAc 100:0 to 50:50), to yield the product as a clear oil (329 mg, 92%). LC-MS B: t _R = 0.93 min; [M+H] ⁺ = 280.37.

C.1.55. 1-(2-Propyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)p henyl)cyclopropane-1-carboxylic acid

The title compound is prepared according to the procedure described for C.1.4., starting with 1 -(4-bromo-2- propylphenyl)cyclopropane-1 -carboxylic acid. LC-MS B: t _R = 1.02 min; [M+MeCN] ⁺ = 372.47. C.1.55.1. 1-(4-Bromo-2-propylphenyl)cyclopropane-1-carboxylic acid

In a flask containing 1-(4-bromo-2-propylphenyl)cyclopropane-1 -carbonitrile (465 mg, 1.69 mmol) and equipped with a condenser, are added successively H ₂ 0 (1.6 mL), AcOH (1.2 mL) and H2SO4 (1.8 mL). The RM is stirred at 1 10°C for 3 d, then cooled to RT. The RM is poured into ice water and the mixture is extracted with DCM (3x). The combined organic layers are washed with NaOH 1 N. The basic aqueous layer is extracted once more with EtOAc. The aqueous layer is acidified till pH2-3 by addition of 2N HCI. This acidic aqueous layer is then extracted twice with EtOAc. These organic layers (acidic extraction) are combined, washed with water, brine, dried over MgSC>4, filtered and concentrated under reduced pressure, affording the title compound as a white solid (283mg, 65%). LC-MS B: tR = 0.96 min; no ionization. ¹ H NMR (400 MHz, d ₆ -DMSO) δ: 12.13-12.49 (m, 1 H), 7.36-7.41 (m, 1 H), 7.23-7.33 (m, 1 H), 7.13-7.22 (m, 1 H), 2.59-2.67 (m, 2 H), 1.61 (m, 2 H), 1.43-1.56 (m, 2 H), 1.06-1.15 (m, 2 H), 0.81-0.98 (m, 3 H).

C.1.55.2. 1-(4-Bromo-2-propylphenyl)cyclopropane-1-carbonitrile

To a solution of 2-(4-bromo-2-propylphenyl)acetonitrile (A.3.42.3., 1180 mg, 4.81 mmol) in toluene (25 mL) are added at RT under argon 1 ,2-dibromoethane (1.26 mL, 14.4 mmol), benzyltriethylammonium chloride (89.4 mg, 0.385 mmol) and NaOH (1346 mg, 33.6 mmol). The RM is stirred over 2 nights at 110°C, it is then cooled to RT and 1 ,2-dibromoethane (1.26 mL, 14.4 mmol), benzyltriethylammonium chloride (89.4 mg, 0.385 mmol) and NaOH (1346 mg, 33.6 mmol) are added and the RM is stirred overnight at 1 10°C. Once at RT, the RM is quenched with water and concentrated in vacuo. The residue is partitioned between EtOAc and water. The aqueous is extracted once more with EtOAc. The combined organic layers are washed with water, brine, dried over MgS04, filtered and concentrated in vacuo. The residue is purified by FC (HepLEtOAc, 100:0 to 95:5), affording the title compound as a yellow oil (468mg 37%). LC-MS B: t _R = 1.06 min; [M+H] ⁺ = 263.92.

C.1.56. 1-(2-Ethoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)cyclopropane-1-carboxylic acid

The title compound is prepared according to the procedure described for C.1.4., starting with 1 -(4-bromo-2- ethoxylphenyl)cyclopropane-1-carboxylic acid. LC-MS B: t _R = 0.96 min; [M+H] ⁺ = 333.44.

C.1.56.1. 1-(4-Bromo-2-ethoxyphenyl)cyclopropane-1-carboxylic acid

The title compound is prepared according to the procedure described for C.1.55.1., starting with 1 -(4- bromo-2-ethoxyphenyl)cyclopropane-1 -carbonitrile. LC-MS B: tR = 0.90 min; [M+H]+ = 285.17.

C.1.56.2. 1-(4-Bromo-2-ethoxyphenyl)cyclopropane-1-carbonitrile

The title compound is prepared according to the procedure described for C.1.55.2., starting with 2-(4-bromo- 2-ethoxyphenyl)acetonitrile(Example 282-d). LC-MS B: t _R = 1.00 min; [M+H] ⁺ = 265.94. C.1.57. Methyl 2-(2-ethoxy-5-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetate (1.880 g, 6.41 mmol) in anh. DMF (20 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.656 g, 6.46 mmol), potassium acetate (2.535 g, 25.80 mmol) and Pd(dppf)CI ₂ (0.525 g, 0.71 mmol). The mixture is heated to 90°C, under nitrogen, overnight. The RM is allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(2-ethoxy-5-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a colorless solid (1.330 g, 61 %). LC-MS B: t _R = 1.05 min; [M+H] ⁺ = 339.23.

C.1.57.1. Methyl 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetate

To a solution of 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetic acid (1.776 g, 6.41 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (3.132 g, 9.61 mmol) and iodomethane (0.60 mL, 9.61 mmol) and the mixture is stirred at RT, under nitrogen, for 30 min. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetate as a clear pink oil (1.880 g, quantitative). LC-MS B: t _R = 0.99 min; [M+H] ⁺ = 291.08.

C.1.57.2. 2-(4-Bromo-2-ethoxy-5-fluorophenyl)acetic acid

A mixture of 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetonitrile (1.738 g, 6.74 mmol), water (6.5 mL), 95% sulfuric acid (7 mL) and acetic acid (8.5 mL) is heated to 1 10°C, under nitrogen, for 3h. The RM is allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure affording 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetic acid as a colorless solid (1.775 g, 95%). LC-MS B: t _R = 0.85 min; no ionization.

C.1.57.3. 2-(4-Bromo-2-ethoxy-5-fluorophenyl)acetonitrile

A solution of 1-bromo-4-(chloromethyl)-5-ethoxy-2-fluorobenzene (1.860 g, 6.95 mmol) in MeCN (18 mL) and water (2.5 mL) is treated with sodium cyanide (0.461 g, 9.04 mmol) and the mixture is heated to 80°C, under nitrogen, overnight. The RM is allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the mixture is extracted twice with DCM. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to EtOAc) affords 2-(4-bromo-2-ethoxy-5-fluorophenyl)acetonitrile as a pale yellow solid (1.734 g, 97%). LC-MS B: t _R = 0.93 min; no ionization.

C.1.57.4. 1-Bromo-4-(chloromethyl)-5-ethoxy-2-fluorobenzene

A cooled (0°C) mixture of (4-bromo-2-ethoxy-5-fluorophenyl)methanol (1.780 g, 7.15 mmol) and zinc chloride (24.4 mg, 0.17 mmol) in anh. DCM (14 mL) is treated dropwise with thionyl chloride (1.04 mL, 14.30 mmol) and the mixture is stirred at 0°C for 3h. The RM is concentrated under reduced pressure affording 1 -bromo- 4-(chloromethyl)-5-ethoxy-2-fluorobenzene as a colorless oil (1.860 g, 97%). LC-MS B: t _R = 1.03 min; no ionization.

C.1.57.5. (4-Bromo-2-ethoxy-5-fluorophenyl)methanol

To a cooled (-78°C) solution of methyl 4-bromo-2-ethoxy-5-fluorobenzoate (2.170 g, 7.83 mmol) in anh. THF (50 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in THF, 23.5 mL, 23.5 mmol) and the mixture is stirred at -78°C, under nitrogen, for 15 min, and then at 0°C for 45 min. The cooled RM is treated successively with water (1 mL), 2.8 N aq. NaOH (1 mL) and water (1 mL) and stirred at RT for 1 h. The resulting mixture is filtered over celite and concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (4-bromo-2-ethoxy-5-fluorophenyl)methanol as a colorless solid (1.780 g, 91 %). LC-MS B: t _R = 0.84 min; no ionization.

C.1.57.6. Methyl 4-bromo-2-ethoxy-5-fluorobenzoate

To a solution of methyl 4-bromo-5-fluoro-2-hydroxybenzoate (1.763 g, 6.73 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (3.287 g, 10.10 mmol) and iodoethane (0.81 1 mL, 10.10 mmol) and the mixture is stirred at RT, under nitrogen, overnight. Water is added and the obtained solid is filtered, washed with water and dried under high vacuum to afford methyl 4-bromo-2-ethoxy-5-fluorobenzoate as a colorless solid (2.170 g, quantitative). LC-MS B: t _R = 0.94 min; [M+H] ⁺ = 277.09.

C.1.58. Methyl 2-(2-ethoxy-3-fluoro-4-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)acetate

To a solution of methyl 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetate (1.939 g, 6.66 mmol) in anh. DMF (20 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (1.708 g, 6.66 mmol), potassium acetate (2.615 g, 26.60 mmol) and Pd(dppf)CI ₂ (0.542 g, 0.73 mmol). The mixture is heated to 90°C, under nitrogen, overnight. The RM is allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(2-ethoxy-3-fluoro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)acetate as a dark green oil (1.254 g, 56%). LC-MS B: t _R = 1.05 min; [M+H] ⁺ = 339.23.

C.1.58.1. Methyl 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetate

To a solution of 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetic acid (2.186 g, 7.28 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (3.213 g, 9.86 mmol) and iodomethane (0.738 mL, 1 1.80 mmol) and the mixture is stirred at RT, under nitrogen, for 15 min. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetate as a clear oil (1.939 g, 91 %). LC-MS B: t _R = 0.99 min; [M+H] ⁺ = 291.10. C.1.58.2. 2-(4-Bromo-2-ethoxy-3-fluorophenyl)acetic acid

A mixture of 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetonitrile (1.879 g, 7.28 mmol), water (7 mL), 95% sulfuric acid (8 mL) and acetic acid (9 mL) is heated to 110°C, under nitrogen, for 1.5h. The RM is then allowed to cool to RT and is poured onto ice/water. The mixture is extracted twice with DCM and the combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated under reduced pressure affording 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetic acid as an off-white solid (2.186 g, quantitative). LC-MS B: tR = 0.85 min; no ionization.

C.1.58.3. 2-(4-Bromo-2-ethoxy-3-fluorophenyl)acetonitrile

A solution of 1-bromo-4-(chloromethyl)-3-ethoxy-2-fluorobenzene (2.124 g, 7.94 mmol) in MeCN (24 mL) and water (3 mL) is treated with sodium cyanide (0.527 g, 10.30 mmol) and the mixture is heated to 80°C, under nitrogen, overnight. The RM is allowed to cool to RT and is diluted with water. Acetonitrile is removed under reduced pressure and the mixture is extracted twice with DCM. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords 2-(4-bromo-2-ethoxy-3-fluorophenyl)acetonitrile as a colorless solid (1.879 g, 92%). LC-MS B: t _R = 0.97 min; no ionization.

C.1.58.4. 1-Bromo-4-(chloromethyl)-3-ethoxy-2-fluorobenzene

A cooled (0°C) mixture of (4-bromo-2-ethoxy-3-fluorophenyl)methanol (1.947 g, 7.82 mmol) and zinc chloride (26.6 mg, 0.19 mmol) in anh. DCM (25 mL) is treated dropwise with thionyl chloride (1.14 mL, 15.60 mmol) and the mixture is stirred at 0°C for 2h. The RM is concentrated under reduced pressure affording 1 -bromo- 4-(chloromethyl)-3-ethoxy-2-fluorobenzene as a clear oil (2.124 g, quantitative). LC-MS B: t _R = 1.06 min; no ionization.

C.1.58.5. (4-Bromo-2-ethoxy-3-fluorophenyl)methanol

To a cooled (-78°C) solution of ethyl 4-bromo-2-ethoxy-3-fluorobenzoate (2.920 g, 10.00 mmol) in anh. THF (30 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in toluene, 30.1 mL, 30.1 mmol) and the mixture is further stirred at -78°C, under nitrogen, for 45 min. The RM is then allowed to warm-up to 0°C and is treated successively with water and with 2.8 N aq. NaOH. EtOAc is added, the layers are separated and the aqueous layer is extracted twice with EtOAc. The combined organic layers are dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords (4-bromo-2-ethoxy-3-fluorophenyl)methanol as a colorless solid (1.947 g, 78%). LC-MS B: t _R = 0.85 min; no ionization.

C.1.58.6. Ethyl 4-bromo-2-ethoxy-3-fluorobenzoate

To a solution of 4-bromo-3-fluoro-2-hydroxybenzoic acid (3.000 g, 12.80 mmol) in anh. DMF (25 mL) at RT are added potassium carbonate (3.529 g, 25.50 mmol) and iodoethane (2.05 mL, 25.50 mmol) and the mixture is stirred at 80°C, under nitrogen, overnight. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 3/1 ) affords ethyl 4-bromo-2-ethoxy-3-fluorobenzoate as a yellow oil (2.920 g, 79%). LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 291.09.

C.1.59. Methyl 2-(3-propyl-5-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acetate

A mixture of methyl 2-(3-propylthiophen-2-yl)acetate (0.600 g, 3.03 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'- bi(1 ,3,2-dioxaborolane) (0.470 g, 1.82 mmol), (1 ,5-cyclooctadiene)(methoxy)iridium(l) dimer (21.5 mg, 0.0325 mmol) and 4,4'-di-tert-butyl-2,2'-bipyridine (20 mg, 0.074 mmol) in THF (15 mL) is degassed with a nitrogen stream and stirred at 80°C, under nitrogen, overnight. The RM is concentrated under reduced pressure and the residue is purified by FC (from heptane to heptane/EtOAc = 7/3) to afford methyl 2-(3-propyl-5-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)thiophen-2-yl)acetate as a clear oil (0.671 g, 68%). LC-MS B: t _R = 1.07 min; [M+H] ⁺ = 325.24.

C.1.59.1. Methyl 2-(3-propylthiophen-2-yl)acetate

A mixture of methyl 2-(3-bromothiophen-2-yl)acetate (1.655 g, 7.04 mmol), potassium n-propyltrifluorborate (1.223 g, 7.74 mmol) and cesium carbonate (6.881 g, 21.10 mmol) in toluene (24 mL) and water (12 mL) is degassed three times with nitrogen. Palladium(ll) acetate (79 mg, 0.35 mmol) and RuPhos (0.346 g, 0.70 mmol) are then added and the mixture is heated to 95°C, under nitrogen, overnight. The RM is allowed to cool to RT, water is added and the mixture is extracted three times with EtOAc. The combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 2-(3-propylthiophen-2-yl)acetate as a yellow oil (1.336 g, 96%). LC-MS B: t _R = 0.94 min; [M+H] ⁺ = 199.26.

C.1.59.2. Methyl 2-(3-bromothiophen-2-yl)acetate

To a solution of 2-(3-bromothiophen-2-yl)acetic acid (2.000 g, 9.05 mmol) in anh. DMF (20 mL) at RT are added cesium carbonate (5.895 g, 18.10 mmol) and iodomethane (1.14 mL, 18.10 mmol) and the mixture is stirred at RT, under nitrogen, for 1 h. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc

= 7/3) affords methyl 2-(3-bromothiophen-2-yl)acetate as a yellow oil (2.183 g, quantitative). LC-MS B: t _R = 0.86 min; no ionization.

C.1.60. Methyl 3-(2-methoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)propanoate

To a solution of methyl 3-(4-bromo-2-methoxyphenyl)propanoate (0.899 g, 3.26 mmol) in anh. DMF (10 mL) are added at RT 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (0.835 g, 3.26 mmol), potassium acetate (1.278 g, 13.00 mmol) and Pd(dppf)CI ₂ (265 mg, 0.35 mmol). The mixture is heated to 90°C, under nitrogen, overnight. The RM is allowed to cool to RT and is filtered through a pad of celite, washing with EtOAc. The filtrate is washed with water and the aqueous layer is extracted twice with EtOAc. The combined organic layers are washed with brine, dried over MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords methyl 3-(2-methoxy-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl)propanoate as a light yellow oil (0.752 g, 72%). LC-MS B: t _R = 1.02 min; [M+H] ⁺ = 321.22.

C.1.60.1. Methyl 3-(4-bromo-2-methoxyphenyl)propanoate

To a solution of 3-(4-bromo-2-methoxyphenyl)propanoic acid (1.000 g, 3.86 mmol) in anh. DMF (10 mL) at RT are added cesium carbonate (2.515 g, 7.72 mmol) and iodomethane (0.485 mL, 7.72 mmol) and the mixture is stirred at RT, under nitrogen, for 1 h. Water and Et ₂ 0 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 7/3) affords methyl 3-(4-bromo-2-methoxyphenyl)propanoate as a clear oil (0.899 g, 85%). LC-MS B: t _R = 0.96 min; no ionization.

C.1.61. Methyl 2-(3-(difluoromethoxy)-5-(4,4,5 _! 5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acetate

A mixture of methyl 2-(3-(difluoromethoxy)thiophen-2-yl)acetate (0.365 g, 1.64 mmol), 4,4,4',4',5,5,5',5'-octamethyl- 2,2'-bi(1 ,3,2-dioxaborolane) (0.253 g, 0.98 mmol), (1 ,5-cyclooctadiene)(methoxy)iridium(l) dimer (1 1 mg, 0.0164 mmol) and 4,4'-di-tert-butyl-2,2'-bipyridine (1 1 mg, 0.039 mmol) in THF (8 mL) is degassed with a nitrogen stream and stirred at 80°C, under nitrogen, overnight. The RM is concentrated under reduced pressure and the residue is purified by FC (from heptane to heptane/EtOAc = 4/1 ) to afford methyl 2-(3-(difluoromethoxy)-5-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophen-2-yl)acetate as a yellow oil (0.473 g, 83%). LC-MS B: t _R = 1.02 min; [M+H] ⁺ = 349.15.

C.1.61.1. Methyl 2-(3-(difluoromethoxy)thiophen-2-yl)acetate

To a solution of 2-(3-(difluoromethoxy)thiophen-2-yl)acetic acid (0.401 g, 1.93 mmol) in anh. DMF (8 mL) at RT are added cesium carbonate (0.941 g, 2.89 mmol) and iodomethane (0.145 mL, 2.31 mmol) and the mixture is stirred at RT, under nitrogen, for 30 min. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords methyl 2-(3-(difluoromethoxy)thiophen-2-yl)acetate as a pale yellow oil (0.364 g, 85%). LC-MS B: t _R = 0.83 min; no ionization.

C.1.61.2. 2-(3-(Difluoromethoxy)thiophen-2-yl)acetic acid

A mixture of 2-(3-(difluoromethoxy)thiophen-2-yl)acetonitrile (0.306 g, 1.62 mmol), potassium hydroxide (0.272 g, 4.85 mmol) in EtOH (3 mL) and water (3 mL) is heated to 1 10°C, under nitrogen, for 2.5h. The RM is allowed to cool to RT and is concentrated under reduced pressure. 1 M aq. HCI and DCM are successively added, the layers are separated and the aqueous layer is extracted twice with DCM. The combined organic layers are washed with brine, dried over anh. MgSCX filtered and concentrated under reduced pressure affording 2-(3-(difluoromethoxy)thiophen-2-yl)acetic acid as an orange oil (0.296 g, 88%). LC-MS B: t _R = 0.68 min; no ionization. C.1.61.3. 2-(3-(Difluoromethoxy)thiophen-2-yl)acetonitrile

A solution of 2-(chloromethyl)-3-(difluoromethoxy)thiophene (0.426 g, 2.14 mmol) in anhydrous DMSO (10.5 mL) is treated with sodium cyanide (0.217 g, 4.29 mmol) and the mixture is heated to 80°C, under nitrogen, for 75 min. The RM is allowed to cool to RT and is diluted with water. The resulting mixture is extracted three times with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 4/1 ) affords 2- (3-(difluoromethoxy)thiophen-2-yl)acetonitrile as a pale yellow oil (0.306 g, 75%). LC-MS B: t _R = 0.78 min; no ionization.

C.1.61.4. 2-(Chloromethyl)-3-(difluoromethoxy)thiophene

A cooled (0°C) mixture of (3-(difluoromethoxy)thiophen-2-yl)methanol (0.360 g, 2.00 mmol) and zinc chloride

(7 mg, 0.049 mmol) in anh. DCM (20 mL) is treated dropwise with thionyl chloride (0.291 mL, 3.99 mmol) and the mixture is stirred at RT for 3h. The mixture is cooled to 0°C, treated dropwise with thionyl chloride (0.291 mL, 3.99 mmol) and further stirred at RT for 1 h. The RM is concentrated under reduced pressure to afford 2- (chloromethyl)-3-(difluoromethoxy)thiophene as a black oil (0.328 g, 83%). LC-MS B: t _R = 0.82 min; no ionization.

C.1.61.5. (3-(Difluoromethoxy)thiophen-2-yl)methanol

To a cooled (-78°C) solution of methyl 3-(difluoromethoxy)thiophene-2-carboxylate (1.450 g, 6.97 mmol) in anh. THF (50 mL) is added dropwise a solution of diisobutylaluminum hydride (1 M in THF, 21.0 mL, 21.0 mmol). The mixture is further stirred at -78°C, under nitrogen, for 20 min and is then allowed to warm-up to 0°C. Stirring at 0°C is continued for 20 min, and the RM is treated successively with water (1 mL), 2.8 N aq.

NaOH (1 mL) and water (2 mL). The mixture is then allowed to warm-up to RT and stirred for 1 h. The resulting mixture was filtered over celite washing with THF and the filtrate was concentrated to dryness under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords (3-(difluoromethoxy)thiophen-2- yl)methanol as a pale yellow oil (1.075 g, 86%). LC-MS B: t _R = 0.63 min; no ionization.

C.1.61.6. Methyl 3-(difluoromethoxy)thiophene-2-carboxylate

To a solution of 3-(difluoromethoxy)thiophene-2-carboxylic acid (0.500 g, 2.45 mmol) in anh. DMF (4 mL) at RT are added successively cesium carbonate (1.196 g, 3.67 mmol) and iodomethane (0.185 mL, 2.94 mmol) and the mixture is stirred at RT for 40 min. Water and Et20 are added and the layers are separated. The aqueous layer is extracted twice with Et20 and the combined organic layers are washed with brine, dried over anh. MgSC>4, filtered and concentrated under reduced pressure. Purification by FC (from heptane to heptane/EtOAc = 1/1 ) affords methyl 3-(difluoromethoxy)thiophene-2-carboxylate as a colorless oil (0.495 g, 97%). LC-MS B: t _R = 0.81 min; no ionization. D- Preparation of examples

General procedure A: Suzuki coupling with Pd(PPh ₃ )4

A mixture of the respective pyrimidine halide derivative (A3) (0.15 mmol), the respective boronic acid derivative (A4) (0.18 mmol), and K ₂ C0 ₃ 2M (0.3 mL, 0.6 mmol) in ethanol (3 mL) is purged with argon, Pd(PPh ₃ ) ₄ (0.0075 mmol) is added, and the RM is heated at 90°C overnight. Alternatively, the reaction can be performed in a MW apparatus, at 120°C for 15 - 30 min. The RM is filtered through a 0.45 urn Glass MicroFiber filter, washed with EtOH/MeCN and DMF. The filtrate is purified either by preparative HPLC or FC. Alternatively, it is diluted with water, if needed the pH is adjusted, and extracted with EtOAc (3x). The combined organic extracts are dried (MgSC>4) and concentrated under reduced pressure. The residue is purified by preparative HPLC or by FC.

General procedure B: Suzuki coupling with Pd(PPh ₃ )4 followed by ester hydrolysis

A mixture of the respective pyrimidine halide derivative (A3) (0.15 mmol), the respective boronic acid derivative (A4) (0.18 mmol), and K ₂ C0 ₃ 2M (0.3 mL, 0.6 mmol) in EtOH (3 mL) is purged with argon, Pd(PPh ₃ ) ₄ (0.0075 mmol) is added, and the RM is heated at 90°C overnight. Alternatively, the reaction can be performed in a MW apparatus, at 120°C for 15 - 30 min. NaOH (32% solution, 0.5 mL) is added, and the RM is stirred at RT for 2 - 20h or at 90°C for 0.5 - 20h. It is then filtered through a 0.45 urn Glass MicroFiber filter, washed with EtOH and water. The filtrate is either purified directly by preparative HPLC or diluted with 1 N HCI, and extracted 3x with EtOAc. The combined organic extracts are dried (MgSC>4) and concentrated under reduced pressure. The residue is purified by preparative HPLC or by FC.

General procedure C: Suzuki coupling with PdCI ₂ (dppf) followed by ester hydrolysis

A mixture of the respective pyrimidine halide derivative (A3) (0.15 mmol), the respective boronic acid derivative (A4) (0.18 - 0.3 mmol), and Cs ₂ C0 ₃ (0.75 mmol) in THF (4 mL) and water (0.5 mL) is purged with argon, [1 ,1 '- bis(diphenylphosphino)ferrocene]dichloropalladium(ll) complex with DCM (0.015 mmol) is added, and the RM is heated at 80°C overnight. NaOH (32% solution, 0.5 mL) is added, and the RM is stirred at 80°C for 2 - 20 h. It is then filtered through a 0.45 urn Glass MicroFiber filter, washed with EtOH and water. The filtrate is either purified directly by preparative HPLC or diluted with 1 N HCI, and extracted 3x with EtOAc. The combined organic extracts are dried (MgS04) and concentrated under reduced pressure. The residue is purified by preparative HPLC or by FC.

General procedure D: phosphonium-mediated SNAr

To a solution of 6-hydroxy-pyrimidine derivative (0.1 mmol) in DMF (1 mL) and TEA (0.4 mmol) is added PyBOP (0.16 mmol). The solution is stirred at RT for 15 min - 1 h, then the respective aryl-ethylamine (0.125 mmol) is added and the RM is stirred at 80°C overnight. The RM is cooled to RT and treated with a few drops of water and purified by preparative HPLC. Alternatively, the RM is diluted with EtOAc and washed twice with brine. The organic layer is dried over MgS04, filtered and concentrated. The residue is purified by preparative HPLC or by FC if needed. Alternatively, a solution of 6-hydroxy-pyrimidine derivative (0.1 mmol) in DMF (1 mL) is treated with DBU (0.15 mmol) and BOP (0.13 mmol). The solution is stirred at RT for 15 min - 1 h, then the respective aryl-ethylamine (0.125 mmol) is added, and the RM is stirred at 80°C for 2 - 20h. The RM is cooled to RT and treated with a few drops of water and purified by preparative HPLC. Or the RM is diluted with EtOAc and washed twice with brine. The organic layer is dried over MgS04, filtered and concentrated. The residue is purified by preparative HPLC or by FC if needed.

Compounds of Examples 1 - 155 listed in Table 4 below are prepared by applying either one of the above-mentioned procedures A, B or C to the pyrimidine halide derivatives A.1.1. - A.1.13., A.2.1. - A.2.3., B.1.1. - B.1.9. coupled with boronic acid derivatives or with boronic acid derivatives C.1.1. - C.1.31.

Table 4: Exam les 1 - 155

4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin-4-

1.0 (C) 479 yl}-2-methylsulfanyl-benzoic acid

4-{6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino ]-pyrimidin-4-yl}-2-

0.9 (C) 477.2 methylsulfanyl-benzoic acid

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-

1.0 (C) 450.3 methylsulfanyl-benzoic acid

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

0.78 (A) 500.12 4-yl}-2-methylsulfanyl-benzoic acid ( )

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzofuran-3-yl)-ethylamino]- pyrimidin-4-yl}-2-

0.77 (A) 452.02 methylsulfanyl-benzoic acid

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.0 (C) 468.2 methylsulfanyl-benzoic acid

4-{6-[2-(2-Methyl-benzofuran-3-yl)-ethylamino]-pyrimidin-4-y l}-2-methylsulfanyl-

0.9 (C) 420.3 benzoic acid ( )

4-{6-[2-(4-Chloro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 484.2 methylsulfanyl-benzoic acid

4-{6-[2-(4,7-Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 504.2 methylsulfanyl-benzoic acid

4-{6-[2-(6-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.0 (C) 468.2 methylsulfanyl-benzoic acid ( )

4-{6-[2-(2-Ethyl-5-fluoro-7-methyl-benzofuran-3-yl)-ethylami no]-pyrimidin-4-yl}-2-

0.80 (A) 466.04 methylsulfanyl-benzoic acid

4-{6-[2-(7-Chloro-5-fluoro-2-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin-4-

1.1 (C) 488.2 yl}-2-methylsulfanyl-benzoic acid ( )

4-{6-[2-(2-Methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimid in-4-yl}-2-

0.9 (C) 436.2 methylsulfanyl-benzoic acid ( )

3- Ethoxy-5-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl) -ethylamino]-pynmidin-

1.2 (C) 472.2

4- yl}-thiophene-2-carboxylic acid

5-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin-4-

1.1 (C) 482.9 yl}-3-ethoxy-thiophene-2-carboxylic acid

5-{6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino ]-pyrimidin-4-yl}-3-

0.88 (A) 480.94 ethoxy-thiophene-2-carboxylic acid

3-Ethoxy-5-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thioph en-3-yl)-ethylamino]-

1.1 (C) 488.2 pyrimidin-4-yl}-thiophene-2-carboxylic acid ( )

5-{6-[2-(4-Chloro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-

1.2 (C) 488.4 ethoxy-thiophene-2-carboxylic acid 5-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.1 (C) 504.2 4-yl}-3-ethoxy-thiophene-2-carboxylic acid ( )

5-{6-[2-(4,5-Difluoro-7-methoxy-2-methyl-benzofuran-3-yl)-et hylamino]-pyrimidin-4-

1.1 (C) 490.3 yl}-3-ethoxy-thiophene-2-carboxylic acid

3- Ethoxy-5-{6-[2-(5-fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.2 (C) 472.2

4- yl}-thiophene-2-carboxylic acid

5-[6-(2-Benzo[b]thiophen-3-yl-ethylamino)-pyrimidin-4-yl]-3- ethoxy-thiophene-2-

1.0 (C) 426.1 carboxylic acid

3-Ethoxy-5-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzofuran-3-y l)-ethylamino]-

1.0 (C) 472.1 pyrimidin-4-yl}-thiophene-2-carboxylic acid

5-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin-4-yl}-3-ethoxy-

1.1 (C) 458.1 thiophene-2-carboxylic acid ( )

5-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyri midin-4-yl}-3-ethoxy-

1.1 (C) 454.1 thiophene-2-carboxylic acid ( )

3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzofuran-3-yl)-eth ylamino]-pyrimidin-4-yl}-

1.1 (C) 456.1 thiophene-2-carboxylic acid ( )

5-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-

1.1 (C) 488 ethoxy-thiophene-2-carboxylic acid ( )

3-Ethoxy-5-{6-[2-(2-ethyl-5-fluoro-7-methyl-benzofuran-3-yl) -ethylamino]-pyrimidin-4-

1.2 (C) 470.1 yl}-thiophene-2-carboxylic acid

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

0.9 (C) 484.1 4-yl}-2-methoxy-benzoic acid

5-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-

1.0 (C) 488 (2-hydroxy-ethoxy)-thiophene-2-carboxylic acid ( )

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-

1.0 (C) 464.1 ethylsulfanyl-benzoic acid

2-Ethylsulfanyl-4-{6-[2-(2-methyl-benzo[b]thiophen-3-yl)-eth ylamino]-pyrimidin-4-yl}-

1.0 (C) 450 benzoic acid

2-Ethylsulfanyl-4-{6-[2-(2-methyl-benzofuran-3-yl)-ethylamin o]-pyrimidin-4-yl}-

1.0 (C) 434.3 benzoic acid

4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 464.2 propyl-benzoic acid

5-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-3-

1.0 (C) 496.3 trifluoromethyl-thiophene-2-carboxylic acid

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-fluoro-6-

1.0 (C) 468.3 methylsulfanyl-benzoic acid 2-Fluoro-4-{6-[2-(2-methyl-benzo[b]thiophen-3-yl)-ethylamino ]-pyrimidin-4-yl}-6-

1.0 (C) 454.1 methylsulfanyl-benzoic acid

2-Fluoro-4-{6-[2-(2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin-4-yl}-6-

0.9 (C) 438.2 methylsulfanyl-benzoic acid

2-Chloro -{6-[2-(2J-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrim idin -yl}-6-

1.1 (C) 484.2 methylsulfanyl-benzoic acid

2-Chloro-4-{6-[2-(2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin-4-yl}-6-

1.0 (C) 454.3 methylsulfanyl-benzoic acid

(3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-

1.1 (C) 485.9 pyrimidin-4-yl}-thiophen-2-yl)-acetic acid

4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin-4-

1.0 (C) 477.3 yl}-2-ethoxy-benzoic acid

4-{6-[2-(2-Cyano-7-methoxy-benzo[b]thiophen-3-yl)-ethylamino ]-pyrimidin-4-yl}-2-

0.9 (C) 475.2 ethoxy-benzoic acid

2-Ethoxy-4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thioph en-3-yl)-ethylamino]-

1.0 (C) 482 pyrimidin-4-yl}-benzoic acid ( )

2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pynmidin-

0.78 (A) 466.20 4-yl}-benzoic acid

4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.0 (C) 498 4-yl}-2-ethoxy-benzoic acid ( )

4-{6-[2-(2-Bromo-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-et hylamino]-pyrimidin -

1.1 (C) 529.3 yl}-2-ethoxy-benzoic acid ( )

4-{6-[2-(2-Chloro-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin4-

1.1 (C) 485.9 yl}-2-ethoxy-benzoic acid ( )

4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin4-yl}-2-ethoxy-

1.0 (C) 448.3 benzoic acid

2-Ethoxy-4-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pynmidin-

1.0 (C) 466.4 4-yl}-benzoic acid

2-Ethoxy-4-{6-[2-(6-fluoro-2,7-dimethyl-benzo[b]thiophen-3-y l)-ethylamino]-pynmidin-

1.0 (C) 466.3 4-yl}-benzoic acid ( )

4-{6-[2-(4,7-Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 502.4 ethoxy-benzoic acid

4-{6-[2-(5-Chloro-2J-dimethyl-benzofuran-3-yl)-ethylamino]-p yrimidin4-yl}-2-ethoxy-

1.1 (C) 465.9 benzoic acid ( )

4-{6-[2-(7-Chloro-5-fluoro-2-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin4-

1.1 (C) 486.2 yl}-2-ethoxy-benzoic acid ( ) 82 2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-1 H-

1.0 (C) 461.3 indole-4-carboxylic acid

83 4-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.0 (C) 494 cyclopropoxy-benzoic acid

84 2-Cyclopropoxy-4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b] thiophen-3-yl)-

1.0 (C) 494.4 ethylamino]-pynmidin-4-yl}-benzoic acid

85 2-Cyclopropoxy -{6-[2-(4,5-difluoro-7-methoxy-2-methyl-benzofuran-3-yl)-

1.0 (C) 496 ethylamino]-pyrimidin-4-yl}-benzoic acid

86 4-{6-[2-(5-fluoro-2J limethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4-yl}- 2-(2-

0.9 (C) 482 hydroxy-ethoxy)-benzoic acid ( )

87 4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-

1.1 (C) 478.1 propylsulfanyl-benzoic acid

88 4-{6-[2-(2-Methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimid in-4-yl}-2-propylsulfanyl-

1.1 (C) 464 benzoic acid

89 4-{6-[2-(2-Methyl-benzofuran-3-yl)-ethylamino]-pyrimidin-4-y l}-2-propylsulfanyl-

1.0 (C) 448.4 benzoic acid

90 4-{6-[2-(2,7-Dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyr imidin-4-yl}-2-

1.1 (C) 478.1 isopropylsulfanyl-benzoic acid

91 2-lsopropylsulfanyl -{6-[2-(2-methyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidi n-4-

1.1 (C) 464.2 yl}-benzoic acid ( )

92 2-lsopropylsulfanyl4-{6-[2-(2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-

1.0 (C) 448.2 benzoic acid ( )

93 2-Fluoro4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl )-ethylamino]-pyrimidin-

1.1 (C) 482 4-yl}-6-propyl-benzoic acid

94 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin4-yl}-2-

1.1 (C) 478 isobutyl-benzoic acid

95 (3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-

1.2 (C) 500.3 pyrimidin4-yl}-thiophen-2-yl)-acetic acid methyl ester

96 fEJ-3-(3-Ethoxy-5-{6-[2-(5-fluoro-2J-dimethyl-benzo[b]thioph en-3-yl)-ethylamino]-

1.2 (C) 498.2 py ri mid i n-4-y l}-th iophen-2-yl )-acr I ic acid

97 3-(3-Ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-

1.1 (C) 500.3 pyrimidin4-yl}-thiophen-2-yl)-propionic acid

98 4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.1 (C) 512.3 4-yl}-2-isopropoxy-benzoic acid

99 4-{6-[2-(6-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 480.3 propoxy-benzoic acid ( ) 100 4-{6-[2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin-4-yl}-2-

1.1 (C) 480 propoxy-benzoic acid

101 4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.1 (C) 512.3 4-yl}-2-propoxy-benzoic acid

102 4-{6-[2-(4J-Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethylam ino]-pyrimidin-4-yl}-2-

1.2 (C) 516.4 propoxy-benzoic acid

103 2-Ethoxy -{6-[2-(4-fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylami no]-pyrimidin-

0.9 (C) 480 4-yl}-6-methyl-benzoic acid

104 (4-{6-[2-(2-Cyano-5-fluoro-7-methyl-benzo[b]thiophen-3-yl)-e thylamino]-pyrimidin-4-

0.9 (C) 491.3 yl}-2-ethoxy-phenyl)-acetic acid

105 (2-Ethoxy-4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiop hen-3-yl)-ethylamino]-

0.9 (C) 496 pyrimidin-4-yl}-phenyl)-acetic acid

106 (4-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyl amino]-pyrimidin-4-yl}-

0.9 (C) 496.1 2-ethoxy-phenyl)-acetic acid

107 (2-Ethoxy-4-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-

0.9 (C) 480.3 pyrimidin-4-yl}-phenyl)-acetic acid

108 (4-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyr imidin-4-yl}-2-ethoxy-

0.9 (C) 466 phenyl)-acetic acid

109 (4-{6-[2-(2J-Dimethyl-benzo[b]thiophen-3-yl)^thylamino]-pyri midin-4-yl}-2-ethoxy-

0.9 (C) 462.3 phenyl)-acetic acid

110 (2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-

0.9 (C) 480.1 pyrimidin-4-yl}-phenyl)-acetic acid

111 (4-{6-[2-(4-Chloro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.0 (C) 496.1 ethoxy-phenyl)-acetic acid ( )

112 (2-Ethoxy-4-{6-[2-(6-fluoro-2,7-dimethyl-benzo[b]thiophen-3- yl)-ethylamino]-

0.9 (C) 480.3 pyrimidin-4-yl}-phenyl)-acetic acid

113 (4-{6-[2-(7-Chloro-5-fluoro-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-4-

1.0 (C) 500 yl}-2-ethoxy-phenyl)-acetic acid ( )

114 (4-{6-[2-(4J-Dichloro-2-methyl-benzo[b]thiophen-3-yl)-ethyla mino]-pyrimidin -yl}-2-

1.0 (C) 516.4 ethoxy-phenyl)-acetic acid ( )

115 2-Difluoromethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thi ophen-3-yl)-ethylamino]-

1.1 (C) 488 pyrimidin-4-yl}-benzoic acid

116 4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.1 (C) 520 4-yl}-2-difluoromethoxy-benzoic acid

117 (2-Ethoxy-4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiop hen-3-yl)-ethylamino]-

0.8 (C) 512.1 pyrimidin-4-yl}-phenoxy)-acetic acid 136 2-Cyclobutoxy-4-{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophe n-3-yl)-ethylamino]-

1.1 (C) 492.3 pyrimidin-4-yl}-benzoic acid

137 4-{6-[2-(7-Chloro-2-methyl-benzofuran-3-yl)-ethylamino]-pyri midin-4-yl}-2-

1.1 (C) 478.3 cyclobutoxy-benzoic acid ( )

138 2-Cyclobutoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophe n-3-yl)-ethylamino]-

1.1 (C) 492 pyrimidin-4-yl}-benzoic acid

139 2-Cyclobutoxy-4-{6-[2-(4-fluoro-7-methoxy-2-methyl-benzofura n-3-yl)-ethylamino]-

1.0 (C) 492 pyrimidin-4-yl}-benzoic acid

140 2-Cyclobutoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzofuran-3-yl )-ethylamino]-pyrimidin-

1.1 (C) 476.3 4-yl}-benzoic acid

141 2-Cyclobutoxy-4-{6-[2-(4,5-difluoro-7-methoxy-2-methyl-benzo furan-3-yl)-

1.1 (C) 510 ethylamino]-pyrimidin-4-yl}-benzoic acid

142 {6-[3-Ethoxy-4-(1 H-tetrazol-5-yl)-phenyl]-pyrimidin-4-yl}-[2-(5-fluoro-2,7-di methyl-

1.0 (C) 490 benzo[b]thiophen-3-yl)-ethyl]-amine

143 3-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-

0.9 (C) 510.3 pyrimidin-4-yl}-phenoxy)-propionic acid ( )

144 2-Butoxy-6-fluoro -{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]-

1.2 (C) 512.3 pyrimidin-4-yl}-benzoic acid

145 N-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-

1.0 (C) 509.4 pyrimidin-4-yl}-phenyl)-oxalamic acid

146 2-Cyclobutoxy-3-fluoro -{6-[2-(4-fluoro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)-

1.1 (C) 526.3 ethylamino]-pyrimidin-4-yl}-benzoic acid

147 4-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin-4-yl}-2-

1.1 (C) 526.3 cyclobutoxy-3-fluoro-benzoic acid

148 2-Cyclobutoxy-6-fluoro -{6-[2-(4-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-

1.2 (C) 510 ethylamino]-pyrimidin-4-yl}-benzoic acid

149 2-Cyclobutoxy-6-fluoro4-{6-[2-(4-fluoro-7-methoxy-2-methyl-b enzo[b]thiophen-3-yl)-

1.1 (C) 526.1 ethylamino]-pyrimidin4-yl}-benzoic acid

150 2-Cyclobutoxy4-{6-[2-(4,5-difluoro-7-methoxy-2-methyl-benzof uran-3-yl)-

1.1 (C) 528.3 ethylamino]-pyrimidin4-yl}-6-fluoro-benzoic acid

151 4-{6-[2-(5-Chloro-7-methoxy-2-methyl-benzofuran-3-yl)-ethyla mino]-pyrimidin4-yl}-2-

1.1 (C) 526.1 cyclobutoxy-6-fluoro-benzoic acid

152 2-Cyclopentyloxy4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiop hen-3-yl)-ethylamino]-

1.2 (C) 506 pyrimidin4-yl}-benzoic acid

153 4-{6-[2-(4-Chloro-7-methoxy-2-methyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-

1.2 (C) 538.1 4-yl}-2-cyclopentyloxy-benzoic acid 154 2-Cyclopent loxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzofuran-3-yl)-ethylam ino]-

1.2 (C) 490.2 pyrimidin-4-yl}-benzoic acid

155 3-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]- pyrimidin-4-yl}-phenyl)-[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(2-ethoxy-4-(6-

1.1 (C) 506.3 ((2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethyl)amino) pyrimidin-4-yl)phenyl)- [1 ,2,4]oxadiazol-5-ol]

Example 156: 3-Ethoxy-5-(6-((2-(5-fluoro-2 -dimethylbenzo[b]thiophen -yl)ethyl)amino)pyrimidin-4-yl)-N- sulfamoylthiophene-2-carboxamide

3-Ethoxy-5-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin

acid (Example 32, 75 mg, 0.159 mmol) is dissolved in DMSO/THF (2:1 ) (3.3 mL) and CDI (38.7 mg, 0.239 mmol) is added. The RM is heated at 60°C for 1 h, cooled to RT and treated with sulfamide (33.6 mg, 0.35 mmol) and DBU (0.0594 mL, 0.398 mmol). The RM is stirred at RT for 2h. HCI 2M (5 mL) is added, the precipitate is filtered, then purified by prep HPLC to yield the title compound as a white solid (29 mg, 33%). LC-MS B: t _R = 0.96 min; [M+H] ⁺ = 550.1 1.

Example 157: N-(3-Ethoxy-5-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4- yl}-thiophene-2-carbonyl)-methanesulfonamide

Following the procedure described for the synthesis of Example 156, with 3-ethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl- benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin -yl}-thiophene-2-carboxylic acid and methanesulfonamide, the title compound is obtained as a white solid. LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 549.13.

Example 158: {6-[4-Ethoxy-5-(1 H-tetrazol-5-yl)4hiophen-2-yl]-pyrimidin-4-yl}-[2-(5-fluoro- 2,7-dimethyl- benzo[b]thiophen-3-yl)-ethyl]-amine

Following the general procedure D with 2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine (A.1.4.1.) and 6-(4-ethoxy-5-(1 H-tetrazol-5-yl)thiophen-2-yl)pyrimidin-4-ol, the title compound is obtained as a brown solid. LC- MS B: t _R = 0.96 min; [M+H] ⁺ = 496.1 1.

a) 6-(4-Ethoxy-5-(1 H-tetrazol-5-yl)thiophen-2-yl)pyrimidin-4-ol

4-(4-Ethoxy-5-(1 H-tetrazol-5-yl)thiophen-2-yl)-6-methoxypyrimidine (30 mg, 0.0986 mmol) is treated with HCI 4M in dioxane (0.5 mL) and the RM is stirred at 55-60 °C overnight. It is then concentrated under reduced pressure and purified by prep. HPLC to afford the title compound as a white solid (12 mg, 42%). LC-MS B: [R = 0.59 min; [M+H] ⁺ = 291.04.

b) 4-(4-Ethoxy-5-(1 H-tetrazol-5-yl)thiophen-2-yl)-6-methoxypyrimidine

To a solution of 3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carbonitrile (72 mg, 0.276 mmol) in toluene (2.1 mL), trimethylsilylazide (0.0544 mL, 0.413 mmol) and dibutyltin oxide (6.86 mg, 0.0276 mmol) are added. The RM is stirred at 110°C overnight in a sealed tube. The solvent is evaporated, then the residue is dissolved in MeOH and adjusted to pH = 10 with NaOH 2M. The solution is loaded onto a PE_AX cartridge for standard catch&release protocol, which affords the title compound as a yellow solid (43 mg, 51 %). LC-MS B: tR = 0.78 min; [M+H] ⁺ = 305.06.

c) 3-Ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carbonitrile

Cyanuric chloride (6248 mg, 33.5 mmol) is added portionwise at 0°C to a suspension of 3-ethoxy-5-(6- methoxypyrimidin-4-yl)thiophene-2-carboxamide (6940 mg, 22.4 mmol) in DMF (130 mL). The RM is then stirred at RT for 45 min. It is cooled at 0°C and diluted with water. The solid is filtered off, washing with water and then EtOAc, and dried under high vacuum. The filtrate is extracted twice with EtOAc, combined organic layers are washed with brine, dried over MgS04, filtered and concentrated under reduced pressure. Both solids are combined to afford the title compound as a beige solid (5.49 g, 94%). LC-MS B: tR = 1.00 min; [M+H] ⁺ = 262.26.

d) 3-Ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carboxamide

CDI (4861 mg, 29.1 mmol) is added to a solution of 3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2- carboxylic acid (7410 mg, 26.4 mmol) in THF (140 mL) at RT. The RM is stirred for 30 min, then NH40H (25% solution, 61.1 mL, 397 mmol) is added, and the RM is stirred at RT for 30min, then concentrated under reduced pressure, and the residue is triturated in 2N HCI. The title compound is filtered off, dried under high vacuum, and obtained as a yellow solid (6.94 g, 94%). LC-MS B: t _R = 0.79 min; [M+H] ⁺ = 280.22.

e) 3-Ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carboxylic acid

A suspension of methyl 3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carboxylate (7870 mg, 26.2 mmol) in MeOH (210 mL) and NaOH 2M (38.8 mL, 419 mmol) is stirred overnight at RT. It is then acidified with HCI 24.5% (8N) (60mL), MeOH is removed under vacuum and the slury is filtered, to afford the title compound as a yellow solid (7.41 g, 99% ). LC-MS B: t _R = 0.77 min; [M+H] ⁺ = 281.19.

f) Methyl 3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carboxylate

A mixture of methyl 3-ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate (10520 mg, 30 mmol), 4-chloro-6-methoxypyrimidine (4645 mg, 31.5 mmol), dichloro(1 ,V-bis(diphenylphosphino) ferrocene) palladium (II) dichloromethane adduct) (2449 mg, 3 mmol) and potassium phosphate tribasic monohydrate (20719 mg, 90 mmol) in water (4 mL) and DMF (150 mL) is degassed for 20 min under a nitrogen stream, then stirred at RT for 1 h15. The RM is filtered through celite, the filtrate is concentrated under vacuum, the residue is partitioned between water and EtOAc. The organic layer is further washed with brine, dried over MgS04, filtered and concentrated. Purification by FC (heptane/EtOAc, from 1 :0 to 0:1 ) affords the title compound as a yellow solid (7.87 g, 89% ). LC-MS B: t _R = 0.93 min; [M+H] ⁺ = 295.18.

f) Methyl 3-ethoxy-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate

The title compound is prepared according to the synthesis of C.1.1. using methyl 3-ethoxythiophene-2- carboxylate, and obtained as a white solid; LC-MS B: t _R = 0.63 min; [M+H] ⁺ = 313.13.

Example 159: 3-(3-Ethoxy-5-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4- yl}-thiophen-2-yl)-[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(3-ethoxy-5-(6-((2-(5-fluoro-2,7- dimethylbenzo[b]thiophen -yl)ethyl)amino)pyrimidin-4-yl)thiophen-2-yl)-[1 ,2,4]oxadiazol-5-ol] (Ί ) Following the general procedure D with 2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1 -amine (A.1.4.1.) and 3-(3-ethoxy-5-(6-hydroxypyrimidin-4-yl)thiophen-2-yl)-[1 ,2,4]oxadiazol-5-ol, the title compound is obtained as a light brown solid. LC-MS B: t _R = 1.03 min; [M+H] ⁺ = 512.12.

a) 3-(3-Ethoxy-5-(6-hydroxypyrimidin-4-yl)thiophen-2-yl)-[1 ,2,4]oxadiazol-5-ol

A suspension of 3-(3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophen-2-yl)-[1 ,2,4]oxadiazol-5-ol (5180 mg, 12.1 mmol) in HCI (4M in dioxane, 100 mL) is heated at 100°C overnight, cooled down to RT, and the solvent is partially removed. The solid residue is filtered off washing with water, and dried under high vacuum, affording the title compound as a light yellow solid. LC-MS B: t _R = 0.66 min; [M+H] ⁺ = 307.01.

b) 3-(3-Ethoxy-5-(6-methoxypyrimidin-4-yl)thiophen-2-yl)-[1,2,4 ]oxadiazol-5-ol

To a mixture of 3-ethoxy-N'-hydroxy-5-(6-methoxypyrimidin -yl)thiophene-2-carboximidamide (6930 mg, 22.6 mmol) and DBU (8.62 mL, 56.5 mmol) in Dioxane/DMSO (3:2, 220 mL) is added CDI (5498 mg, 33.9 mmol). The RM is stirred at 100°C for 30min, then cooled to RT. Evaporation of the solvent and trituration in 2N HCI affords the title compound as a yellow solid (7.15 g, 99%). LC-MS A: t _R = 0.89 min; [M+H] ⁺ = 321.14. c) 3-Ethoxy-N'-hydroxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-c arboximidamide

A suspension of 3-ethoxy-5-(6-methoxypyrimidin-4-yl)thiophene-2-carbonitrile (Example 158-c, 6860 mg, 24.7 mmol), TEA (10.3 mL, 74 mmol) and hydroxylamine hydrochloride (2.59 mL, 61.7 mmol) in EtOH (220 mL) is refluxed for 3h, then cooled to RT and treated with water (30 mL)The yellow solid is filtered off and dried under high vacuum. The filtrate is concentrated and the solid is triturated in water, filtered off and combined with the first crop. The title compound is obtained as a yellow solid (6.93 g, 95%). LC-MS B: t _R = 0.62 min; [M+H] ⁺ = 295.23.

Example 160: 4-Ethoxy-2-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen -yl)-ethylamino]^yrimidin-4-yl}- thiazole-5-carboxylic acid

To a solution of ethyl 4-ethoxy-2-(6-hydroxypyrimidin-4-yl)thiazole-5-carboxylate (59 mg, 0.2 mmol) in DMF (2 mL) are added TEA (0.14 mL, 1.0 mmol) and PyBop (156 mg, 0.3 mmol). The RM is stirred at RT for a few minutes until complete dissolution and 2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine (A.1.4.1.) (56 mg, 0.25 mmol) is added. The RM is heated at 100 °C for 30 min in the MW apparatus. NaOH 10% (0.721 mL, 2 mmol) is added and the RM is stirred at 70°C overnight. Purification by prep. LC-MS affords the title compound as a yellow solid. LC-MS B: t _R = 1.01 min; [M+H] ⁺ = 473.1 1.

a) Ethyl 4-ethoxy-2-(6-hydroxypyrimidin-4-yl)thiazole-5-carboxylate

Following the procedure described for the synthesis of Example 159-a with ethyl 4-ethoxy-2-(6- methoxypyrimidin-4-yl)thiazole-5-carboxylate, the title compound is obtained as a yellow solid. LC-MS B: t _R = 0.78 min; [M+H] ⁺ = 296.15.

b) Ethyl 4-ethoxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carboxylate

To a solution of ethyl 4-hydroxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carboxylate (1730 mg, 6.15 mmol) in DMF (40 mL) at RT under argon is added K ₂ C0 ₃ (2168 mg, 15.4 mmol), and the RM is heated at 60°C. lodoethane (0.749 mL, 9.23 mmol) is added and the RM is stirred at 75°C overnight. It is then cooled to RT, and water (75 mL) is added. The aq layer is extracted with DCM, the organic extracts are dried (MgSC>4), filtered and concentrated under reduced pressure, affording the crude title compound as an orange solid (1.75 g, 76%). LC-MS B: t _R = 1.04 min; [M+H] ⁺ = 310.24.

c) Ethyl 4-hydroxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carboxylate

To a solution of 6-methoxypyrimidine-4-carbothioamide (1000 mg, 5.85 mmol) in toluene (40 mL) is added pyridine (1.9 mL, 23.4 mmol) at RT, followed by diethyl bromomalonate (1.52 mL, 8.19 mmol). The RM is heated at reflux overnight, then cooled to RT and treated with HCI 2N. The product is filtered off. The layers of the filtrate are separated and the aq layer is extracted twice with EtOAC. The combined organic layers are dried over MgSC>4, filtered, evaporated to dryness. The residue is combined with the first crop, yielding the title compound as a brown solid (1.73 g, 99%). LC-MS B: t _R = 0.89 min; [M+H] ⁺ = 282.18.

Example 161 : 4-Ethyl-2-{6-[2-(5-fluoro-2 J-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4-yl }- thiazole-5-carboxylic acid

Following the procedure described for the synthesis of Example 160, using 2-(5-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethan-1-amine (A.1.4.1.) and ethyl 4-ethyl-2-(6-hydroxypyrimidin-4-yl)thiazole-5- carboxylate, the title compound is obtained as a yellow solid. LC-MS B: t _R = 1.01 min; [M+H] ⁺ = 457.02.

a) Ethyl 4-ethyl-2-(6-hydroxypyrimidin-4-yl)thiazole-5-carboxylate

Following the procedure described for the synthesis of Example 159-a with ethyl 4-ethyl-2-(6-ethoxypyrimidin- 4-yl)thiazole-5-carboxylate, the title compound is obtained as a beige solid. LC-MS B: t _R = 0.73 min; [M+H] ⁺ = 266.26.

b) Ethyl 4-ethyl-2-(6-ethoxypyrimidin-4-yl)thiazole-5-carboxylate

To a solution of methyl 2-chloro-3-oxovalerate (0.96 mL, 6.5 mmol) in EtOH (30 mL) is added 6- methoxypyrimidine-4-carbothioamide (1000 mg, 5.91 mmol) and the mixture is refluxed overnight. Methyl 2- chloro-3-oxovalerate (1.31 mL, 8.86 mmol) is added and the RM is further refluxed for 24h, then cooled at RT and treated with water (15 mL), cooled down to 0°C. The precipitate is filtered off, rinsed with MeOH and dried under high vacuum, affording the title compound as a pinkish solid (485 mg, 28%). LC-MS B: t _R = 1.07 min;

[M+H] ⁺ = 294.20.

Example 162: 3-(4-Ethoxy-2-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimidin-4- yl}-thiazol-5-yl)-[1,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(4-ethoxy-2-(6-((2-(5-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethyl)amino)pyrimidin-4-yl)thi azol-5-yl)-[1,2,4]oxadiazol-5-ol] (Ί ) Following the general procedure D with 2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine (A.1.4.1.) and 3-(4-ethoxy-2-(6-hydroxypyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol, the title compound is obtained as a yellow solid. LC-MS B: t _R = 1.14 min; [M+H] ⁺ = 513.02.

a) 3-(4-Ethoxy-2-(6-hydroxypyrimidin-4-yl)thiazol-5-yl)-[1,2,4] oxadiazol-5-ol

Following the procedure described for the synthesis of Example 159-a with 3-(4-ethoxy-2-(6- methoxypyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol, the title compound is obtained as a yellowish solid.

LC-MS B: tR = 0.68 min; [M+H] ⁺ = 308.17. b) 3-(4-Ethoxy-2-(6-methoxypyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol

Following the procedure described for the synthesis of Example 159-b with 4-ethoxy-N'-hydroxy-2-(6- methoxypyrimidin-4-yl)thiazole-5-carboximidamide, the title compound is obtained as a beige solid. LC-MS B: t _R = 0.94 min; [M+H] ⁺ = 321.93.

c) 4-Ethoxy-N'-hydroxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-ca rboximidamide

Following the procedure described for the synthesis of Example 159-c with 4-ethoxy-2-(6-methoxypyrimidin- 4-yl)thiazole-5-carbonitrile, the title compound is obtained as a deep yellow solid. LC-MS B: tR = 0.67 min; [M+H] ⁺ = 296.17.

d) 4-Ethoxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carbonitrile

NH4OH (25%, 4.05 mL, 26.3 mmol) and I2 (1824 mg, 7.19 mmol) are added at 0°C to a solution of 4-ethoxy-

2-(6-methoxypyrimidin-4-yl)thiazole-5-carbaldehyde (465 mg, 1.75 mmol) in THF (15 mL) and the mixture is stirred at RT for 3h. It is then poured in 10mL of NaHS0 ₃ 40% (15 mL) and extracted with EtOAc, dried over MgSC>4 and concentrated under vacuum, to afford the title compound as an orange solid. LC-MS B: tR = 1.02 min; [M+H] ⁺ = 263.25.

e) 4-Ethoxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carbaldehyde

A mixture of ethyl 4-ethoxy-2-(6-methoxypyrimidin-4-yl)thiazole-5-carboxylate (Example 147-b, 706 mg, 2.64 mmol) in THF (20 mL) is cooled down to -78°C and DiBAI-H (1 M in THF, 5.28 mL, 5.28 mmol) is added dropwise. The mixture is stirred at RT overnight. The mixture is quenched at 0°C by dropwise addition of water (200 uL), then NaOH 10% (400uL) and finally water (600 uL). The aluminium precipitate is filtered over a pad of Celite and rinced with EtOAc. The filtrate is dried over MgSC>4, filtered and concentrated under reduced pressure. The residue is dissolved in DCM (20 mL) and Mn02 (2701 mg, 26.4 mmol) is added. The mixture is stirred 5h at RT, then filtered over a pad of Celite and rinced with EtOAc. The filtrate is concentrated under reduced pressure, affording the title compound as a light orange solid. LC-MS B: tR = 0.97 min; [M+H] ⁺ = 266.25.

Example 163: 3-(4-Ethyl-2-{6-[2-(5-fluoro-2 -dimethyl-benzo[b]thiophen -yl)-ethylamino]^yrimidin-4-yl}- thiazol-5-yl)-[1 ,2,4]oxadiazol-5(4H)-one [tautomeric form: 3-(4-ethyl-2-(6-((2-(5-fluoro-2,7- dimethylbenzo[b]thiophen-3-yl)ethyl)amino)pyri

Following the general procedure D, using 3-(4-ethyl-2-(6-hydroxypyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol and 2-(5-fluoro-2,7-dimethylbenzo[b]thiophen-3-yl)ethan-1-amine (A.1.4.1.), the title compound is obtained as a yellow solid. LC-MS B: t _R = 1.09 min; [M+H] ⁺ = 497.00.

a) 3-(4-Ethyl-2-(6-hydroxypyrimidin-4-yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol

Following the procedure described for the synthesis of Example 159-a with 3-(4-ethyl-2-(6-ethoxypyrimidin-4- yl)thiazol-5-yl)-[1 ,2,4]oxadiazol-5-ol, the title compound is obtained as a grey solid. LC-MS B: tR = 0.64 min; [M+H] ⁺ = 292.17.

b) 3-(4-Ethyl-2-(6-ethoxypyrimidin-4-yl)thiazol-5-yl)-[1,2,4]ox adiazol-5-ol Following the procedure described for the synthesis of Example 159-b with 4-ethyl-N'-hydroxy-2-(6- ethoxypyrimidin-4-yl)thiazole-5-carboximidamide, the title compound is obtained as a light orange solid. LC- MS B: t _R = 0.92 min; [M+H] ⁺ = 320.21.

c) 4-Ethyl-N'-hydroxy-2-(6-ethoxypyrimidin-4-yl)thiazole-5-carb oximidamide

Following the procedure described for the synthesis of Example 159-c with 4-ethyl-2-(6-ethoxypyrimidin-4- yl)thiazole-5-carbonitrile, the title compound is obtained as a light yellow solid. LC-MS B: tR = 0.66 min; [M+H] ⁺ = 294.21.

d) 4-Ethyl-2-(6-ethoxypyrimidin-4-yl)thiazole-5-carbonitrile

Following the procedure described for the synthesis of Example 158-c with 2-(6-ethoxy pyri mi d i n-4-yl )-4- ethylthiazole-5-carboxamide, the title compound is obtained as a beige solid. LC-MS A: tR = 1.04 min; [M+H] ⁺

= 261.29.

e) 2-(6-Ethoxypyrimidin-4-yl)-4-ethylthiazole-5-carboxamide

Following the procedure described for the synthesis of Example 158-d with 2-(6-ethoxypyrimidin-4-yl)-4- ethylthiazole-5-carboxylic acid, the title compound is obtained as an orange solid. LC-MS B: tR = 0.79 min; [M+H] ⁺ = 279.25.

f) 2-(6-Ethoxypyrimidin-4-yl)-4-ethylthiazole-5-carboxylic acid

An ice-chilled solution of ethyl 4-ethyl-2-(6-ethoxypyrimidin-4-yl)thiazole-5-carboxylate (Example 161 -b, 1000 mg, 3.09 mmol) in THF/MeOH 1 :1 (15 mL) is treated with NaOH 10% (5.58 mL, 15.5 mmol) and stirred at RT for 20h. The solvents are removed under reduced pressure, the aqueous phase is extracted once with Et20.The aqueous phase is then acidified with 2N HCI and extracted with EtOAc (3 x). The combined organic extracts are dried over MgS04, fitlered and concentrated under reduced pressure, yielding the title compound as a greenish solid (522 mg, 64%). LC-MS B: t _R = 0.88 min; [M+H] ⁺ = 280.24.

Compounds of Examples 164 - 205 listed in Table 5 below are prepared by applying either one of the above- mentioned procedures A, B or C to the pyrimidine halide derivatives A.1.1. - A.1.15. coupled with boronic acid derivatives or with boronic acid derivatives C.1.1. - C.1.54.

Table 5: Exam les 164 - 205

Example 206: 4-{6-[2-(5-Fluoro-2J-dimethyl-benzo[b]thiophen-3-yl)-ethylam ino]^yrimidin-4-yl}-2- propyl-benzamide

To a solution of 4-{6-[2-(5-fluoro-2 ,7-dimethyl-benzo[b]thiophen-3-yl)-ethylamino]-pyrimidin-4-y l}-2-propyl-benzoic acid (Example 45, 0.08 mmol), ammonium chloride (5.7 mg, 0.096 mmol), DIPEA (0.0438 mL, 0.256 mmol) in DMF (0.6 mL) is added a solution of HATU (31.9 mg, 0.084 mmol) in DMF (0.2 mL). The RM is stirred for 3 d at RT, then directly purified by prep LC-MS, affording the title compound as a white solid (15 mg, 40%). LC-MS C: t _R = 0.926 min; [M+H] ⁺ = 463.3.

Following the procedure described for Example 206, with 4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-pyrimidin-4-yl}-2-propyl-benzoic acid (Example 45) and the corresponding commercially available amines, the following examples are synthesized:

Table 6

Ex. Compound tR [min] MS Data m/z

(LC-MS C) [M+H] ⁺

207 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]- 0.974 535 pyrimidin-4-yl}-N-(2-hydroxy-2-methyl-propyl)-2-propyl-benza mide

208 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]- 1.003 521.2 pyrimidin-4-yl}-N-(2-methoxy-ethyl)-2-propyl-benzamide

209 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]- 0.897 507.3 pyrimidin-4-yl}-N-(2-hydroxy-ethyl)-2-propyl-benzamide

210 4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]- 0.965 477.2 pyrimidin-4-yl}-N-methyl-2-propyl-benzamide Following the procedure described for Example 206, with 2-ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-ethylamino]-pyrimidin-4-yl}-benzoic acid (Example 56) and the corresponding commercially available amines, the following examples are synthesized:

Table 7

By applying either one of the above-mentioned General Procedures A, B or C to the pyrimidine halide derivatives A.1.1. - A.1.15. coupled with commercial boronic acid derivatives or with boronic acid derivatives C.1.1. - C.1.XX, the following examples are synthesized:

t _R [min] (LC- MS Data m/z

Ex. Compound

MS method) [M+H] ⁺

2-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)- ethylamino]-

214 0.824 (C) 454.3 pyrimidin-4-yl}-pyrazol-1-yl)-2-methyl-propionic acid ( )

1-(2-Ethoxy-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]thiophen- 3-yl)-

215 0.97 (C) 506.2 ethylamino]-pyrimidin-4-yl}-phenyl)-cyclopropanecarboxylic acid ( )

(2-Ethoxy-3-fluoro-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]th iophen-3-

216 0.985 (C) 498.3 yl)-ethylamino]-pyrimidin-4-yl}-phenyl)-acetic acid ( )

(2-Ethoxy-5-fluoro-4-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]th iophen-3-

217 1.01 (C) 498.3 yl)-ethylamino]-pyrimidin-4-yl}-phenyl)-acetic acid ( )

1-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-

218 1.015 (C) 504.1 pyrimidin-4-yl}-2-propyl-phenyl)-cyclopropanecarboxylic acid ( )

(5-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyl amino]-

219 1.126 (C) 484.3 pyrimidin-4-yl}-3-propyl-thiophen-2-yl)-acetic acid ( )

(3-Difluoromethoxy-5-{6-[2-(5-fluoro-2,7-dimethyl-benzo[b]th iophen-

220 1.187 (C) 508.2 3-yl)-ethylamino]-pyrimidin-4-yl}-thiophen-2-yl)-acetic acid ( )

2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-

221 1.197 (C) 461.3 py ri m id i n-4-y I}- 1 H-indole-7-carboxylic acid ( ) 2-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-ethyla mino]-

222 1.262 (C) 478.2 pyrimidin-4-yl}-benzo[b]thiophene-7-carboxylic acid ( )

3-(4-{6-[2-(5-Fluoro-2,7-dimethyl-benzo[b]thiophen-3-yl)-eth ylamino]-

223 0.62 (B) 480.24 pyrimidin-4-yl}-2-methoxy-phenyl)-propionic acid ( )

II. Biological Assays

Compounds of the present invention may be further characterized with regard to their general pharmacokinetic and pharmacological properties using conventional assays well known in the art such as angiogenesis assays or tumor growth inhibition assays, or for example relating to their bioavailablility in different species (such as rat or dog); or for their properties with regard to drug safety and/or toxicological properties using conventional assays well known in the art, for example relating to cytochrome P450 enzyme inhibition and time dependent inhibition, pregnane X receptor (PXR) activation, glutathione binding, or phototoxic behavior.

Tumor growth inhibition assay

EMT-6 mouse tumor model

The EMT-6 cell line is established from a transplantable murine mammary carcinoma that arose in a BALB/cCRGL mouse after implantation of a hyperplastic mammary alveolar nodule (Volence FJ, et al, J Surg Oncol. 1980, 13(1 ):39-44), obtained from ATCC (American Type culture collection, Manassas, Virginia, USA).

EMT-6 tumour cells are grown as monolayer at 37°C in a humidified atmosphere (5% C02, 95% air) in RPM1 1640 containing 2mM L glutamine supplemented with 10% fetal bovine serum. For experimental use, tumour cells are detached from the culture flask with trypsin. The cells are counted in a hemocytometer and their viability is assessed by trypan blue exclusion.

Tumours are induced in female BALB/c mice by either subcutaneous injection of 1 x10 ⁶ EMT-6 cells in 200 μί of RPM1 1640 into the right flank or by injection of 2.5x10 ⁵ EMT-6 cells in 50 μΐ of RPMI1640 into the mammary fat pad tissue. For the latter injection, female BALB/c mice are anaesthetized with Isoflurane and a 5 mm incision is made in the skin over the lateral thorax to expose the mammary fat pad tissue. After tumor cell injection the thoracic surface is gently dabbed with a 95% ethanol-dampened cotton-swab to kill tumor cells that may leak from the injection site. The skin of mice is closed with 4-0 crinerce sutures.

Animals are monitored daily for behavior and survival and twice weekly for body weight and tumor growth. Tumor size is measured with calipers and tumor volume is calculated according to the following formula: Tumor volume = (width ² x length)/2.

When tumors reach between 60 and 100mm ³ (depending on the experiment), treatment with EP2 and/or EP4 antagonists is started and compound is given daily for at least 3 weeks.

Tumor weight is measured at the end of the study. Biological in vitro Assays

The antagonistic activities of the compounds of formula (I) on the EP2 and EP4 receptors are determined in accordance with the following experimental method.

The assay is using the PathHunterTM HEK 293 PTGER2 and PTGER4 b-arrestin cell lines from DiscoverX. The system is based on the Enzyme Fragment Complementation Technology. Two complementing fragments of the b- galactosidase enzyme are expressed within stably transfected cells. The larger portion of b-gal, termed EA for Enzyme Acceptor, is fused to the C-terminus of b-arrestin 2. The smaller fragment, termed ProLinkTM tag, is fused to PTGER2 (EP2) or PTRGER4 (EP4) at the C-terminus. Upon activation, b-arrestin is recruited which forces the interaction of ProLink and EA, allowing complementation of the two fragments of b-gal and the formation of a functional enzyme which is capable of hydrolysing the substrate and generating a chemiluminescent signal. hEP2 b-arrestin assay:

The HEK 293 PTGER2 b-arrestin cells (DiscoverX 93-021 -4C1 ) are detached from culture dishes with a cell dissociation buffer (Invitrogen, 13151-014), and collected in growing medium (GM: DMEM + Glutamax-I (Invitrogen 32430) /10% FCS, 1 % Penicilin/streptomycin). 5000 cells per well of a 384 well plate (white with white bottom Greiner 781080 ) are seeded in 20ul per well of GM. Plate is incubated at 37°C, 5% C02 for 24 hours.

Stock solutions of test compounds are made at a concentration of 10 mM in DMSO, and serially diluted in DMSO to concentrations required for inhibition dose response curves (tested concentration range 10μΜ-2ηΜ or 1 μΜ- 0.2nM).

PGE2 (Cayman 14010, stock solution: 10mM in DMSO) is used as agonist at 5μΜ final concentration, corresponding to EC80.

Five microliters of diluted compounds are transferred into the assay plate. Plate is pre-incubated 15 minutes at 37°C. Then five microliters of PGE2 (final cone. 5μΜ) are transferred into the assay plate. Plate is incubated 120 minutes at 37°C.

PathHunter Glo Detection Kit components are thawed and mix according to manufacturer's instructions : 1 part Galacton Star Substrate with 5 parts Emerald IITM Solution, and 19 parts of PathHunter Cell Assay Buffer, respectively. Twelve μΙ of reagent are transferred to the assay plate and incubate for 1 hour at room temperature in the dark. Luminescence counts are read on a BMG Fluostar Optima reader according to manufacturer's instructions.

For each compound concentration calculate of the percentage of activity compared to DMSO control value as average ± STDEV. (each concentration is measured in duplicate)

IC ₅ o values and curves are generated with XLfit software (IDBS) using Dose-Response One Site model 203. When compounds were measured multiple times, mean values are given. hEP4 b-arrestin assay:

The HEK 293 PTGER4 b-arrestin cells (DiscoverX 93-030-4C1 ) are detached from culture dishes with a cell dissociation buffer (Invitrogen, 13151-014), and collected in growing medium (GM: DMEM + Glutamax-I (Invitrogen 32430) /10% FCS, 1 % Penicilin/streptomycin). 5000 cells per well of a 384 well plate (white with white bottom Greiner 781080 ) are seeded in 20ul per well of GM. Plate is incubated at 37°C, 5% C02 for 24 hours.

Stock solutions of test compounds are made at a concentration of 10 mM in DMSO, and serially diluted in DMSO to concentrations required for inhibition dose response curves (tested concentration range 10μΜ-2ηΜ or 1 μΜ- 0.2nM).

PGE2 (Cayman 14010, stock solution: 100uM in DMSO) is used as agonist at 20nM final concentration, corresponding to EC80.

Five microliters of diluted compounds are transferred into the assay plate. Plate is pre-incubated 15 minutes at 37°C. Then five microliters of PGE2 (final cone. 20nM) are transferred into the assay plate. Plate is incubated 120 minutes at 37°C.

PathHunter Glo Detection Kit components are thawed and mix according to manufacturer's instructions : 1 part Galacton Star Substrate with 5 parts Emerald IITM Solution, and 19 parts of PathHunter Cell Assay Buffer, respectively. Twelve μΙ of reagent are transferred to the assay plate and incubate for 1 hour at room temperature in the dark. Luminescence counts are read on a BMG Fluostar Optima reader according to manufacturer's instructions.

For each compound concentration calculate of the percentage of activity compared to DMSO control value as average ± STDEV. (each concentration is measured in duplicate)

IC50 values and curves are generated with XLfit software (IDBS) using Dose-Response One Site model 203. When compounds were measured multiple times, mean values are given.

The antagonistic activities of the compounds of formula (I) on the EP2 and EP4 receptors are also determined in accordance with the following experimental method.

Human tumor cell lines expressing endogenously either EP4 or EP2 are used and cAMP accumulation in cells upon PGE2 stimulation is monitored. SF295 glioblastoma cells express high endogenous EP2 and no EP4,whereas BT549 breast cancer cells, express high endogenous EP4 levels and very low EP2 levels.

As a detection method for cAMP the HTRF (homogeneous time resolved fluorescence) Cisbio kit (HTRF cAMP dynamic 2 kit 20Ό00 tests Cisbio Cat. #62AM4PEC) was used, which is based on a competitive immunoassay using a Cryptate-labeled anti-cAMP antibody and d2-labeled cAMP. Native cAMP produced by cells or unlabeled cAMP (for the standard curve) compete with exogenously added d2-labeled cAMP (acceptor) for binding to monoclonal anti-cAMP-Eu3+ Cryptate (donor). A FRET signal (Fluorescence Resonance Energy Transfer) is obtained only if the labeled anti-cAMP antibody binds the d2 labelled cAMP, thus the specific signal (i.e. energy transfer) is inversely proportional to the concentration of cAMP in the standard or sample.

hEP2 cAMP assay:

The SF295 cells (NCI/No. 0503170) are detached from culture dishes with a cell dissociation buffer (Invitrogen, 13151 -014), and collected in growing medium (GM: RPMI1640 (Invitrogen 21875) /10% FCS, 1 % Penicilin/streptomycin). Cells are counted washed and resuspended in assay buffer (AB; HBSS, 20mM HEPES, 0.2% BSA; 2mM IBMX ). 4Ό00 cells in 5μΙ of AB are seeded per well of a small volume 384 well plate (black with flat bottom, Greiner 784076).

Stock solutions of test compounds are made at a concentration of 10 mM in DMSO, and serially diluted in DMSO to concentrations required for inhibition dose response curves (tested concentration range 30μΜ - 0.4nM; 30μΜ - 0.015ηΜ θΓ ΐμΜ - 0.01 ηΜ).

PGE2 (Cayman 14010, stock solution: 75μΜ in DMSO) is used as agonist at 75nM final concentration, corresponding to EC80.

Two point five microliters of diluted compounds are transferred into the assay plate. Plate is pre-incubated 45 minutes at room temperature. Subsequently, 2.5 microliters of PGE2 (final cone. 75nM) are transferred into the assay plate. Plate is incubated 30 minutes at room temperature. Five μΙ of each donor (anti-cAMP cryptate) and acceptor (cAMP-d2) are added and the plate is incubated another hour at room temperature in the dark and then read using a BMG LABTECH PHERAstar reader (Excitation : 337nm, Emission : 620 and 665nm).

The obtained Delta F (fluorescence) values (665nm/620nM) are converted into % cAMP values using the measurements of the cAMP calibrator provided in the kit. For each compound concentration the percentage of cAMP compared to DMSO control value as average ± STDEV (each concentration is measured in duplicate) is calculated.

IC50 values and curves are generated with XLfit software (IDBS) using Dose-Response One Site model 203. When compounds were measured multiple times, mean values are given.

hEP4 cAMP assay:

The BT549 cells (NCI/No. 0507282) are detached from culture dishes with a cell dissociation buffer (Invitrogen, 13151 -014), and collected in growing medium (GM: RPMI1640 (Invitrogen 21875) /10% FCS, 1 % Penicilin/streptomycin). Cells are counted washed and resuspended in assay buffer (AB; HBSS, 20mM HEPES, 0.2% BSA; 2mM IBMX ). 4Ό00 cells in 5μΙ of AB are seeded per well of a small volume 384 well plate (black with flat bottom, Greiner 784076).

Stock solutions of test compounds are made at a concentration of 10 mM in DMSO, and serially diluted in DMSO to concentrations required for inhibition dose response curves (tested concentration range 30μΜ - 0.4nM; 30μΜ - 0.015ηΜ θΓ ΐμΜ - 0.01 ηΜ). PGE2 (Cayman 14010, stock solution: 6μΜ in DMSO) is used as agonist at 6nM final concentration, corresponding to EC80.

Two point five microliters of diluted compounds are transferred into the assay plate. Plate is pre-incubated 45 minutes at room temperature. Subsequently, 2.5 microliters of PGE2 (final cone. 6nM) are transferred into the assay plate. Plate is incubated 30 minutes at room temperature. Five μΙ of each donor (anti-cAMP cryptate) and acceptor (cAMP-d2) are added and the plate is incubated another hour at room temperature in the dark and then read using a BMG LABTECH PHERAstar reader (Excitation : 337nm, Emission : 620 and 665nm).

The obtained Delta F (fluorescence) values (665nm/620nM) are converted into % cAMP values using the measurements of the cAMP calibrator provided in the kit. For each compound concentration the percentage of cAMP compared to DMSO control value as average ± STDEV (each concentration is measured in duplicate) is calculated.

IC50 values and curves are generated with XLfit software (IDBS) using Dose-Response One Site model 203. When compounds were measured multiple times, mean values are given.

Antagonistic activities of exemplified compounds are displayed in Table 8 (in cAMP assays, except for compounds marked with * measured in beta-arrestin):

Table 8

Ex. hEP2 hEP4 hEP2 hEP4 Ex. hEP2 hEP4 hEP2 hEP4 b-arr IC50 b-arr IC50 cAMP cAMP b-arr IC50 b-arr IC50 cAMP cAMP

1 59 142 22 113 209 284 765

2 25 189 23 117 114 246 477 781

3 18 202 18 222 115 16 208 8 60

4 11 262 33 394 116 30 297 35 223

5 106 247 177 479 117 20 23 101 54

6 5 673 4 549 118 16 29 112 87

7 283 577 198 624 119 21 143 119 1 10

8 16 1 170 8 369 120 29 290 59 123

9 118 1650 44 550 121 27 75 155 129

10 58 1040 32 860 122 14 83 40 136

11 99 3090 71 123 142 359 219

12 4 112 4 20 124 26 115 310

13 51 114 32 27 125 359 426

14 4 195 6 105 126 104 423 233 425

15 6 168 21 134 127 16 225 106 873 13 391 21 189 128 37 82

5 248 9 243 129 6 1410 15 795

1 1200 1 414 130 12 193 20 980

12 414 83 468 131 12 1220 22 625

30 762 26 532 132 58 561 167 166

4 283 24 564 133 25 74 68 170

101 493 172 661 134 27 893 46 194

9 488 27 667 135 14 235 30 198

3 3420 4 795 136 13 155 91 411

2 7 8 1 137 15 258 49 423

1 2 138 14 269 75 478

2 11 4 139 51 209 245 481

2 5 11 5 140 37 1420 72 580

14 25 14 9 141 140 340 11 1 582

10 18 8 11 142 12 41 38 105

11 27 10 13 143 52 63 86 1 15

2 16 2 13 144 26 92 26 1 12

19 168 17 18 145 13 76 271

6 12 6 22 146 47 357 47 243

3 35 2 36 147 213 873 117 889

1 26 4 44 148 30 43 109 238

2 42 2 49 149 13 67 114 241

9 12 12 80 150 109 363 97 450

31 50 28 112 151 60 163 95 631

48 680 94 433 152 27 337 84 581

13 42 153 46 157 212 827

4 328 14 224 154 47 91 1 70 901

3 1080 4 497 155 18 47 87 108

1 1020 4 1380 156 5 26 10 163

20 57 48 147 157 8 42 18 69

46 93 31 30 158 6 7 4 20

10 807 12 989 159 3 11 5

5 3380 2 160 15 16 10 18

2 3620 1 161 61 256 27 363

18 432 13 605 162 6 5 35 51 10 3490 1 163 26 17 20 429

46 133 95 231 164 504 50 348 17

9 34 7 44 165 28 54 129 40

194 60 77 47 166 31 254 183 1 130

15 117 40 138 167 5 34 11 29

13 47 19 186 168 65 66 3030 2990

17 287 44 220 169 30 100 142 30

12 454 17 278 170 19 19 116 13

15 625 12 285 171 59 57 275 42

7 372 15 344 172 40 166 50 70

22 245 60 356 173 8 757

12 499 14 393 174 135 723

27 461 64 445 175 89 492

11 522 7 546 176 9 19 37 12

16 428 15 565 177 47 212

27 407 101 607 178 48 331

73 369 142 635 179 8 184

14 659 39 714 180 20 120

24 668 74 760 181 126 423

37 394 80 985 182 41 164 617 378

7 958 10 1030 183 40 210

3 2250 8 1590 184 7 31 1 39 553

5 3500 4 185 50 134

273 644 186 22 242 309 252

8 4300 9 1 160 187 79 425

10 1 140 39 523 188 98 694

6 1310 8 130 189 20 92 27 121

7 87 190 28 200 274 219

26 263 106 91 191 45 135

13 20 306 192 72 261

202 392 323 193 18 667

13 155 21 138 194 47 96 326 71

22 101 44 11 1 195 4 11 1 6 48

21 80 21 117 196 16 99 50 100

68 374 49 258 197 85 146 86 19 4520 11 289 198 77 175

87 5 318 15 451 199 5 363

88 21 1030 11 695 200 63 550

89 10 1030 5 1 140 201 34 351

90 11 247 35 338 202 17 100 75 297

91 20 843 10 539 203 16 239

92 6 816 6 672 204 108 1030

93 36 35 362 205 74 771

94 45 92 302 206 10 288

95 484 647 855 207 26 335

96 20 16 121 42 208 62 837

97 49 84 120 105 209 8 280

98 55 340 53 216 210 19 469

99 5 238 30 450 211 30 367

100 12 299 20 457 212 11 667

101 22 505 85 482 213 10 405

102 26 810 54 867 214 237 388

103 79 521 11 1 331 215 143 151

104 36 161 48 30 216 41 234

105 33 58 157 125 217 126 847

106 159 396 247 218 95 143

107 38 167 249 255 219 41 21 1

108 31 107 264 220 44 407

109 24 405 95 290 221 24 908

110 25 403 160 296 222 14 453

111 197 561 433 223 35 487

112 42 665 188 450