Substituted benzodiazoles and use thereof in therapy

Abstract

There is provided herein a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R1, R2, X1, X2, Y1 to Y4, Z1 to Z3 and n have meanings provided in the description.

Description

FIELD OF THE INVENTION

The present invention relates to novel compounds, compositions comprising such compounds, and the use of such compounds and compositions in medicine. In particular, the present invention relates to the use of such compounds and compositions in methods for the treatment of cell proliferation disorders, such as in the treatment of inflammation and cancers, which treatment is thought to occur through inhibition of OGG1.

BACKGROUND OF THE INVENTION

The listing or discussion of an apparently prior-published document in this specification should not necessarily be taken as an acknowledgement that the document is part of the state of the art or is common general knowledge.

Reactive oxygen species (ROS) are involved in a range of human pathologies (see, for example, C. Nathan, and A. Cunningham-Bussel, Nat. Rev. Immunol. 13 (2013) 349-361). While ROS are important signalling molecules that stimulate cell growth and are necessary for normal cellular processes, excessive generation of ROS as a result of inflammation or cancer leads to damage to macromolecules. In DNA, guanine is particularly prone to oxidation, resulting in 7,8-dihydro-8-oxoguanine (8-oxoG) in DNA—a well-established biomarker for ROS-mediated pathologies (see: X. Ba, et al., Int. J. Mol. Sci. 15 (2014) 16975-16997; and K. D. Jacob, et al., Mech. Ageing Dev. 134 (2013) 139-157). DNA repair pathways allow cells to cope with high ROS and are highly sought-after therapeutic targets. In mammals, 8-oxoG is primarily recognized and repaired by 8-oxoguanine-DNA glycosylase 1 (OGG1), which is the quantitatively dominant repair activity for oxidized guanines in mammals (see: A. Klungland, et al., Proc. Natl. Acad. Sci. USA. 96 (1999) 13300-5; and E. C. Friedberg, DNA repair and mutagenesis, 2nd ed., ASM Press, Washington, D.C., 2006).

In cancer, activation of oncogenes contributes to genomic instability through replication stress at an early step in carcinogenesis (see T. D. Halazonetis, V. G. Gorgoulis, and J. Bartek, Science. 319 (2008) 1352-1355). While the mechanistic details underlying replication stress are far from clear, we know that at least a subset of oncogenes such as c-Myc and Ras confer an increase in reactive oxygen species and DNA damage (see: O. Vafa, et al., Mol. Cell. 9 (2002) 1031-1044; and A. C. Lee, et al., J. Biol. Chem. 274 (1999) 7936-7940). Multiple lines of evidence show that a high load of reactive oxygen species drive cancer cell proliferation and metastasis at the cost of suffering oxidative damage to macromolecules (see Y. Zhang, et al., Antioxid. Redox Signal. 15 (2011) 2867-2908). Deficiencies in this repair system may lead to increased mutagenesis or cell death after oxidative stress (see: S. Oka, et al., EMBO J. 27 (2008) 421-432; and M. Ohno, et al., Sci. Rep. 4 (2014)).

Mice knockout for Ogg1 are not particularly prone to cancer (see A. Klungland, et al., Proc. Natl. Acad. Sci. USA. 96 (1999) 13300-5), suggesting that functional 8-oxodG avoidance pathways protect cancer cells against the negative effects of the oxidative stress phenotype. OGG1 overexpression protects cells against Ras-induced senescence (see Z. M. Ramdzan, et al., PLoS Biol. 12 (2014)) and OGG1 expression is correlated with lower genomic instability in a panel of adenocarcinoma cell lines (see M. Romanowska, et al., Free Radic. Biol. Med. 43 (2007) 1145-1155) as well as the cellular response to ROS-inducing chemotherapeutics such as paclitaxel (see H.-L. Huang, et al., Cell. Physiol. Biochem. 42 (2017) 889-900). In tumour cells, reducing the capacity to eliminate oxidized guanines from DNA by inhibiting OGG1 activity will reduce cancer cell survival and hence will represent promising novel anticancer therapy, either as monotherapy in cancer forms with high oxidative stress levels and/or in combination with radiotherapy and chemotherapy drugs.

Current treatments of cancer are not effective for all patients with diagnosed disease, including a large proportion of patients that experience adverse effects from treatments with existing therapies or where resistance to on-going therapy is developed over time. The present invention aims at providing new cancer treatments, based on the inhibition of the OGG1 enzyme. OGG1 inhibitors may be used as treatment alone or in combination with other established chemotherapeutics.

Acute and chronic inflammation causes an elevation of ROS and an accumulation of oxidative DNA damage, primarily 8-oxoG (see: C. Nathan, and A. Cunningham-Bussel, Nat. Rev. Immunol. 13 (2013) 349-361; and X. Ba, et al., Int. J. Mol. Sci. 15 (2014) 16975-16997) and in particular at promoter regions (see: L. Pan, et al., J. Biol. Chem. (2016); and L. Pan, et al., Sci. Rep. 7 (2017) 43297). This DNA lesion, present in the genome or as a free repair product in blood and urine, is a biomarker for ongoing lung exposure to pollutants (see: Y. Tsurudome, et al., Carcinogenesis. 20 (1999) 1573-1576; and B. Malayappan, et al., J. Chromatogr. A. 1167 (2007) 54-62) and lung inflammations such as asthma (see C. Hasbal, et al., Pediatr. Allergy Immunol. 21 (2010) e674-e678) and chronic obstructive pulmonary disease (COPD) (see: G. Deslee, et al., Chest. 135 (2009) 965-974; and T. Igishi, et al., Respirology. 8 (2003) 455-460). Cells depend on OGG1 as the most important repair enzyme for removing 8-oxoG from DNA (see H. E. Krokan, and M. Bjøraå, Perspect. Biol. 5 (2013)) and the absence of ROS (see C. Nathan, and A. Cunningham-Bussel, Nat. Rev. Immunol. 13 (2013) 349-361) or OGG1 (see: L. Pan, et al., J. Biol. Chem. (2016); E. Touati, et al., Helicobacter. 11 (2006) 494-505; A. Bacsi, et al., DNA Repair. 12 (2013) 18-26; G. Li, et al., Free Radic. Biol. Med. 52 (2012) 392-401; L. Aguilera-Aguirre, et al., J. Immunol. 193 (2014) 4643-4653; X. Ba, et al., J. Immunol. 192 (2014) 2384-2394; and J. G. Mabley, et al., C., FASEB J. (2004)) reduces the inflammatory response in cells and animals.

Since Ogg1^−/− mice are protected against inflammation (see: E. Touati, et al., Helicobacter. 11 (2006) 494-505; A. Bacsi, et al., DNA Repair. 12 (2013) 18-26; G. Li, et al., Free Radic. Biol. Med. 52 (2012) 392-401; and J. G. Mabley, et al., FASEB J. (2004)), but otherwise viable and largely healthy (see: A. Klungland, et al., Proc. Natl. Acad. Sci. USA. 96 (1999) 13300-5; and O. Minowa, et al., Proc. Natl. Acad. Sci. USA. 97 (2000) 4156-61), a small molecule inhibitor of OGG1 would be expected to alleviate excessive chronic and/or acute inflammations without inducing toxic side effects.

Various disclosures (for example: N. Donley, et al., ACS Chem. Biol. 10 (2015) 2334-2343; Tahara et al., J. Am. Chem. Soc., 140(6) (2018) 2105-2114; and WO 2017/011834 A1) describe screening campaigns for small molecule OGG1 inhibitors.

Nevertheless, at present treatment of diseases caused by excessive inflammation is inefficient for many patients. These patients may suffer from a failure to alleviate the inflammation or serious adverse effects of current treatments.

Thus, there exists a clear and significant need for new treatments for inflammatory diseases based on immunomodulatory effects that can be achieved by inhibition of the OGG1 enzyme. Such methods for the alleviation of inflammation may be achieved by a mechanism that is distinct from any other established or experimental treatment for inflammation and may be used alone or in combination with established medicines. Moreover, such methods may also be broadly applicable to the treatment of a range of disorders relating to abnormal cell proliferation, such as in the treatment of cancers.

SUMMARY OF THE INVENTION

It has now been unexpectedly found that certain substituted benzodiazoles are able to act as inhibitors of OGG1, and thus have properties rendering them useful for the treatment or prevention of cell proliferation disorders.

In a first aspect of the invention, therefore, there is provided a compound of formula I

• • or a pharmaceutically acceptable salt thereof, wherein:
  • X¹ and X² each independently represent O or S;
  • each of Y¹ to Y⁴ independently represents CH or CR³,
  • or any one of Y¹ to Y⁴ may alternatively represent N;
  • either Z¹ and Z² both represent methylene optionally linked by an additional ethylene group,
  • or Z¹ represents ethylene and Z² represents methylene;
  • Z³ represents CH, CR¹ or N;
  • each R¹ independently represents, where possible
    • (i) halo, oxy, —NO₂, —CN, —R^1a, —OR^1b, —S(O)_qR^1c, —S(O)_r(R^1d)(R^1e), —N(R^1f)S(O)_sR^1g, —N(R^1h)(R¹ⁱ), —C(O)OR^1j, or —C(O)NR^1kR^1l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from A¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from A², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from A³;
  • n represents 0 to 11, as appropriate;
  • R² represents
    • (i) phenyl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —NO₂, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —S(O)_rN(R^2d)(R^2e), —N(R^2f)S(O)_sR^2g, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁷,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from A⁸, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁹;
  • each R^1a and R^2a independently represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B⁴;
  • each R^1b to R^1l and R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B⁴;
  • each of A¹ to A⁹ independently represents
    • (i) halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ)—C(O)OR^3j, or —C(O)NR^3kR^3l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and D², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D³;
  • each B¹ independently represents
    • (i) halo, NO₂, —CN, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶;
  • each B² to B⁴ independently represents
    • (i) halo, NO₂, —CN, —R^4a, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4e)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁴,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁶;
  • each R^3a and R^4a represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and E³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E⁴;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and E³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E⁴;
  • each D¹ to D⁶ independently represents
    • (i) halo, NO₂, —CN, —R^5a, —OR^5b, —S(O)_qR^5c, —S(O)_rN(Rd)(R^5e), —N(R^5f)S(O)_sR^5g, —N(R^5h)(R⁵ⁱ), —C(O)OR^5j, or —C(O)NR^5kR^5l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and G², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G³;
  • each E¹ independently represents
    • (i) halo, NO₂, —CN, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e), —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁴,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from G⁵, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁶;
  • each E² to E⁴ independently represents
    • (i) halo, NO₂, —CN, —R^6a, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e), —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G⁴,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and G⁵, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G⁶;
  • each R^5a and R^6a represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and J³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J⁴;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹;
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J²,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and J³, or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J⁴;
  • each G¹ to G⁶ independently represents
    • (i) halo, NO₂, —CN, —R^7a, —OR^7b, —S(O)_qR^7c, —S(O)_rN(R^7d)(R^7e), —N(R^7f)S(O)_sR^7g, —N(R^7h)(R⁷ⁱ), —C(O)OR^7j, or —C(O)NR^7kR^7l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and L², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L³;
  • each J¹ independently represents
    • (i) halo, NO₂, —CN, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j, or —C(O)NR^8kR^8l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from L¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from L², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from L³;
  • each J² to J⁴ independently represents
    • (i) halo, NO₂, —CN, —R^8a, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j, or —C(O)NR^8kR^8l,
    • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L¹,
    • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and L², or
    • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L³;
  • each R^7a and R^8a represent C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^7b to R^7l, and R^8b to R^8l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each L¹ to L³ independently represents halo, NO₂, —CN, —R^9a, —OR^9b, —S(O)_qR^9c, —S(O)_rN(R^9d)(R^9e), —N(R^9f)S(O)_sR^9g, —(R^9h)(R⁹ⁱ), —C(O)OR^9j, or —C(O)NR^9kR^9l,
  • each R^9a independently represents C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^9b to R^9l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro; and
  • each q, r and s independently represents 0, 1 or 2,
  • which compounds (including pharmaceutically acceptable salts) may be referred to herein as the “compounds of the invention”.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1: OGG1 inhibitors selectively decrease the viability of cancer cells

The cell lines from Table 3 are grouped according to pathology and plotted. A. EC50 values for Example 13. The difference between EC50 values of cancer and normal cell lines is significant (P<1E-7, Student's T-test). B. EC50 values for Example 28. The difference between EC50 values of cancer and normal cell lines is significant (P<1E-7, Student's T-test). C. EC50 values for Example 50. The difference between EC50 values of cancer and normal cell lines is significant (P<1E-5, Student's T-test). All values are derived using the method 2 or 3, after a five day incubation.

FIG. 2: OGG1 inhibitor synergize with MTH1 inhibitors and paclitaxel

A3 T-cell leukemia cell line was incubated with the indicated concentrations of Example 13 together with a dilution series of the MTH1 inhibitor Karonudib, as well as paclitaxel. Viability was assessed after a three-day incubation using method 4. A. Viability of A3 cells exposed to the OGG1 inhibitor Example 13 and/or the MTH1 inhibitor Karonudib (Berglund, U., et al. “Validation and Development of MTH1 Inhibitors for Treatment of Cancer.” Annals of Oncology, (2016)). B. Combination index calculation of the results in panel A. A combination index<0.7 indicates synergism. C. Viability of A3 cells exposed to the OGG1 inhibitor Example 13 and/or the tubulin poison paclitaxel. D. Combination index calculation of the results in panel C. A combination index<0.7 indicates synergism.

FIG. 3: OGG1 inhibitor synergize with MTH1 inhibitors Karonudib and AZ #19

A3 T-cell leukemia cell line was incubated with the indicated concentrations of Example 13 together with a dilution series of the MTH1 inhibitor Karonudib or the MTH1 inhibitor AZ #19 (4-((4-Chloro-2-fluorophenyl)amino)-6,7-dimethoxy-N-methylquinoline-3-carboxamide) (Kettle et. al., J. Med. Chem. 2016, 59, 2346-2361). Viability was assessed after a three-day incubation using method 4. A. Viability of A3 cells exposed to the OGG1 inhibitor Example 13 and/or the MTH1 inhibitor Karonudib. B. Viability of A3 cells exposed to the OGG1 inhibitor Example 13 and/or the MTH1 inhibitor AZ #19.

FIG. 4: OGG1 deficiency inhibits cell proliferation in A3 cells

A. A3 cells harbouring doxycycline-inducible shRNA constructs targeting the endogenous OGG1 (sh1, sh2 and sh3) and/or expressing an exogenous OGG1 isoform targeted to mitochondria (OGG1-2A) were added doxycycline and counted at the indicated times. B. Native A3 cells were grown in the presence of 10 μM Example 13 or vehicle and counted at the indicated times. Relative cell numbers were determined according to Method 4.

FIG. 5: OGG1 deficiency and inhibition is toxic in cancer cells

A. OGG1 knockdown inhibits colony formation in H460 lung cancer cells. B. Example 13 inhibits colony formation in the cancer cell lines ACHN and H460, but not in the normal cell lines MRC5 and Ogg1^−/− mouse embryonic fibroblasts. Surviving colonies were determined according to Method 6.

FIG. 6: Example 13 reduces pro-inflammatory gene regulation induced by the cytokine TNFα in MLE-12 cells

Individual genes encoding pro-inflammatory cytokines and chemokines are plotted along the horizontal axis, and the fold change of the indicated treatment compared to non-treated cells is shown on the vertical axes. A. gene regulatory signature of Example 13 compared to non-treated cells. B. gene regulatory signature of 20 ng/ml TNFα. C. gene regulatory signature of 20 ng/ml TNFα and 5 μM Example 13.

FIG. 7: Example 13 reduces recruitment of neutrophils to mouse airways

A. 20 ng TNFα was delivered into each mouse lung intranasally and 25 mg/kg Example 13 was injected intraperitoneally. Lungs were lavaged after 16 h and the number of macrophages and neutrophils was counted. B. 20 ng lipopolysaccharide was delivered intranasally into each mouse lung intranasally and 25 mg/kg Example 13 was injected intraperitoneally. Lungs were lavaged after 16 h and the number of macrophages and neutrophils was counted.

DETAILED DESCRIPTION OF THE INVENTION

For the avoidance of doubt, the skilled person will understand that references herein to compounds of particular aspects of the invention (such as the first aspect of the invention, i.e. referring to compounds of formula I as defined in the first aspect of the invention) will include references to all embodiments and particular features thereof, which embodiments and particular features may be taken in combination to form further embodiments and features of the invention.

Unless indicated otherwise, all technical and scientific terms used herein will have their common meaning as understood by one of ordinary skill in the art to which this invention pertains.

Pharmaceutically acceptable salts include acid addition salts and base addition salts. Such salts may be formed by conventional means, for example by reaction of a free acid or a free base form of a compound of the invention with one or more equivalents of an appropriate acid or base, optionally in a solvent, or in a medium in which the salt is insoluble, followed by removal of said solvent, or said medium, using standard techniques (e.g. in vacuo, by freeze-drying or by filtration). Salts may also be prepared using techniques known to those skilled in the art, such as by exchanging a counter-ion of a compound of the invention in the form of a salt with another counter-ion, for example using a suitable ion exchange resin.

Particular acid addition salts that may be mentioned include carboxylate salts (e.g. formate, acetate, trifluoroacetate, propionate, isobutyrate, heptanoate, decanoate, caprate, caprylate, stearate, acrylate, caproate, propiolate, ascorbate, citrate, glucuronate, glutamate, glycolate, α-hydroxybutyrate, lactate, tartrate, phenylacetate, mandelate, phenylpropionate, phenylbutyrate, benzoate, chlorobenzoate, methylbenzoate, hydroxybenzoate, methoxybenzoate, dinitrobenzoate, o-acetoxy-benzoate, salicylate, nicotinate, isonicotinate, cinnamate, oxalate, malonate, succinate, suberate, sebacate, fumarate, malate, maleate, hydroxymaleate, hippurate, phthalate or terephthalate salts), halide salts (e.g. chloride, bromide or iodide salts), sulphonate salts (e.g. benzenesulphonate, methyl-, bromo- or chloro-benzenesulphonate, xylenesulphonate, methanesulphonate, ethanesulphonate, propanesuphonate, hydroxy-ethanesulphonate, 1- or 2-naphthalene-sulphonate or 1,5-naphthalene-disuphonate salts) or sulphate, pyrosulphate, bisulphate, sulphite, bisulphite, phosphate, monohydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate or nitrate salts, and the like.

Particular base addition salts that may be mentioned include salts formed with alkali metals (such as Na and K salts), alkaline earth metals (such as Mg and Ca salts), organic bases (such as ethanolamine, diethanolamine, triethanolamine, tromethamine and lysine) and inorganic bases (such as ammonia and aluminium hydroxide). More particularly, base addition salts that may be mentioned include Mg, Ca and, most particularly, K and Na salts.

For the avoidance of doubt, compounds of the invention may exist as solids, and thus the scope of the invention includes all amorphous, crystalline and part crystalline forms thereof, and may also exist as oils. Where compounds of the invention exist in crystalline and part crystalline forms, such forms may include solvates, which are included in the scope of the invention.

For the avoidance of doubt, compounds of the invention may also exist in solution (i.e. in solution in a suitable solvent). For example, compounds of the invention may exist in aqueous solution, in which case compounds of the invention may exist in the form of hydrates thereof.

Compounds of the invention may contain double bonds and, unless otherwise indicated, may thus exist as E (entgegen) and Z (zusammen) geometric isomers about each individual double bond. Unless otherwise specified, all such isomers and mixtures thereof are included within the scope of the invention.

Compounds of the invention may also exhibit tautomerism. All tautomeric forms and mixtures thereof are included within the scope of the invention (particularly those of sufficient stability to allow for isolation thereof).

Compounds of the invention may also contain one or more asymmetric carbon atoms and may therefore exhibit optical and/or diastereoisomerism (i.e. existing in enantiomeric or diastereomeric forms). Diastereoisomers may be separated using conventional techniques, e.g. chromatography or fractional crystallisation. The various stereoisomers (i.e. enantiomers) may be isolated by separation of a racemic or other mixture of the compounds using conventional, e.g. fractional crystallisation or HPLC, techniques. Alternatively the desired enantiomer or diastereoisomer may be obtained from appropriate optically active starting materials under conditions which will not cause racemisation or epimerisation (i.e. a ‘chiral pool’ method), by reaction of the appropriate starting material with a ‘chiral auxiliary’ which can subsequently be removed at a suitable stage, by derivatisation (i.e. a resolution, including a dynamic resolution; for example, with a homochiral acid followed by separation of the diastereomeric derivatives by conventional means such as chromatography), or by reaction with an appropriate chiral reagent or chiral catalyst, all of which methods and processes may be performed under conditions known to the skilled person. Unless otherwise specified, all stereoisomers and mixtures thereof are included within the scope of the invention.

For the avoidance of doubt, the skilled person will understand that where a particular group is depicted herein as being bound to a ring system via a floating bond (i.e. a bond not shown as being bound to a particular atom within the ring), the relevant group may be bound to any suitable atom within the relevant ring system (i.e. the ring within which the floating bond terminates).

Unless otherwise specified, C_1-z alkyl groups (where z is the upper limit of the range) defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of two or three, as appropriate) of carbon atoms, be branched-chain, and/or cyclic (so forming a C_3-z cycloalkyl group). When there is a sufficient number (i.e. a minimum of four) of carbon atoms, such groups may also be part cyclic (so forming a C_4-z partial cycloalkyl group). For example, cycloalkyl groups that may be mentioned include cyclopropyl, cyclopentyl and cyclohexyl. Similarly, part cyclic alkyl groups (which may also be referred to as “part cycloalkyl” groups) that may be mentioned include cyclopropylmethyl. When there is a sufficient number of carbon atoms, such groups may also be multicyclic (e.g. bicyclic or tricyclic) and/or spirocyclic. For the avoidance of doubt, particular alkyl groups that may be mentioned include straight chain (i.e. not branched and/or cyclic) alkyl groups. Other alkyl groups that may be mentioned include straight chain and branched (i.e. non-cyclic) alkyl groups.

Unless otherwise specified, C_2-z alkenyl groups (where z is the upper limit of the range) defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of three) of carbon atoms, be branched-chain, and/or cyclic (so forming a C_4-z cycloalkenyl group). When there is a sufficient number (i.e. a minimum of five) of carbon atoms, such groups may also be part cyclic. For example, part cyclic alkenyl groups (which may also be referred to as “part cycloalkenyl” groups) that may be mentioned include cyclopentenylmethyl and cyclohexenylmethyl. When there is a sufficient number of carbon atoms, such groups may also be multicyclic (e.g. bicyclic or tricyclic) or spirocyclic. For the avoidance of doubt, particular alkenyl groups that may be mentioned include straight chain (i.e. not branched and/or cyclic) alkenyl groups. Other alkenyl groups that may be mentioned include straight chain and branched (i.e. non-cyclic) alkenyl groups.

Unless otherwise specified, C_2-z alkynyl groups (where z is the upper limit of the range) defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of four) of carbon atoms, be branched-chain. For the avoidance of doubt, particular alkynyl groups that may be mentioned include straight chain (i.e. not branched and/or cyclic) alkynyl groups. Other alkynyl groups that may be mentioned include straight chain and branched (i.e. non-cyclic) alkynyl groups.

For the avoidance of doubt, unless otherwise specified, groups referred to herein as “alkyl”, “alkenyl” and/or “alkynyl” will be taken as referring to the highest degree of unsaturation in a bond present in such groups. For example, such a group having a carbon-carbon double bond and, in the same group, a carbon-carbon triple bond will be referred to as “alkynyl”. Alternatively, it may be particularly specified that that such groups will comprise only the degree of unsaturation specified (i.e. in one or more bond therein, as appropriate; e.g. in in one bond therein).

For the avoidance of doubt, alkyl, alkenyl and alkynyl groups as described herein may also act as linker groups (i.e. groups joining two or more parts of the compound as described), in which case such groups may also be referred to as “alkylene”, “alkenylene” and/or “alkynylene” groups, respectively.

In some embodiments, any alkyl, alkenyl or alkynyl, more particularly is alkyl (i.e. a saturated, linear branched or cyclic aliphatic moiety, such as methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl etc).

Furthermore, in some embodiments, any C_1-6 alkyl more particularly is C_1-4 alkyl, any C_2-6 alkenyl more particularly is C_2-4alkenyl, and any C_2-6 alkynyl more particularly is C_2-4 alkynyl. In some further of the above embodiments, any C_1-6 alkyl more particularly is C_1-3 alkyl, any C_2-6 alkenyl more particularly is C_2-3 alkenyl, and any C_2-6 alkynyl more particularly is C_2-3 alkynyl.

For the avoidance of doubt, as used herein, references to heteroatoms will take their normal meaning as understood by one skilled in the art. Particular heteroatoms that may be mentioned include phosphorus, selenium, tellurium, silicon, boron, oxygen, nitrogen and sulfur (e.g. oxygen, nitrogen and sulfur, such as oxygen and nitrogen).

As used herein, the term heterocyclyl may refer to non-aromatic monocyclic and polycyclic (e.g. bicyclic) heterocyclic groups (which groups may, where containing a sufficient number of atoms, also be bridged) in which at least one (e.g. one to four) of the atoms in the ring system is other than carbon (i.e. a heteroatom), and in which the total number of atoms in the ring system is between three and twelve (e.g. between five and ten, such as between three and eight; for example, forming a 5- or 6-membered heterocyclyl group). Further, such heterocyclyl groups may be saturated, forming a heterocycloalkyl, or unsaturated containing one or more carbon-carbon or, where possible, carbon-heteroatom or heteroatom-heteroatom double and/or triple bonds, forming for example a C_2-z (e.g. C_4-z) heterocycloalkenyl (where z is the upper limit of the range) or a C_7-z heterocycloalkynyl group.

For the avoidance of doubt, the skilled person will understand that heterocyclyl groups that may form part of compounds of the invention are those that are chemically obtainable, as known to those skilled in the art. Various heterocyclyl groups will be well-known to those skilled in the art, such as 7-azabicyclo-[2.2.1]heptanyl, 6-azabicyclo[3.1.1]heptanyl, 6-azabicyclo[3.2.1]-octanyl, 8-azabicyclo[3.2.1]octanyl, aziridinyl, azetidinyl, 2,3-dihydroisothiazolyl, dihydropyranyl, dihydropyridinyl, dihydropyrrolyl (including 2,5-dihydropyrrolyl), dioxolanyl (including 1,3-dioxolanyl), dioxanyl (including 1,3-dioxanyl and 1,4-dioxanyl), dithianyl (including 1,4-dithianyl), dithiolanyl (including 1,3-dithiolanyl), imidazolidinyl, imidazolinyl, isothiazolidinyl, morpholinyl, 7-oxabicyclo[2.2.1]heptanyl, 6-oxabicyclo[3.2.1]-octanyl, oxetanyl, oxiranyl, piperazinyl, piperidinyl, pyranyl, pyrazolidinyl, pyrrolidinonyl, pyrrolidinyl, pyrrolinyl, quinuclidinyl, sulfolanyl, 3-sulfolenyl, tetrahydropyranyl, tetrahydrofuryl, tetrahydropyridinyl (such as 1,2,3,4-tetrahydropyridinyl and 1,2,3,6-tetrahydropyridinyl), thietanyl, thiiranyl, thiolanyl, tetrahydrothiopyranyl, thiomorpholinyl, trithianyl (including 1,3,5-trithianyl), tropanyl and the like.

Particular heterocyclyl groups that may be mentioned include morpholinyl (e.g. morpholin-4-yl).

Substituents on heterocyclyl groups may, where appropriate, be located on any atom in the ring system including a heteroatom. Further, in the case where the substituent is another cyclic compound, then the cyclic compound may be attached through a single atom on the heterocyclyl group, forming a spirocyclic compound. The point of attachment of heterocyclyl groups may be via any suitable atom in the ring system, including (where appropriate) a further heteroatom (such as a nitrogen atom), or an atom on any fused carbocyclic ring that may be present as part of the ring system. Heterocyclyl groups may also be in the N- or S-oxidized forms, as known to those skilled in the art.

At each occurrence when mentioned herein, particular heterocyclyl groups that may be mentioned include 3- to 8-membered heterocyclyl groups (e.g. a 4- to 6-membered heterocyclyl group, such as a 5- or 6-membered heterocyclyl group). Any such heterocyclyl will include at least one heteroatom, e.g. from 1 to 4 heteroatoms, e.g. from 1 to 3 heteroatoms, in particular 1 or 2 heteroatoms, which heteroatoms preferably are selected from N, O and S, e.g. from N and O.

For the avoidance of doubt, references to polycyclic (e.g. bicyclic or tricyclic) groups (for example when employed in the context of heterocyclyl or cycloalkyl groups (e.g. heterocyclyl)) will refer to ring systems wherein at least two scissions would be required to convert such rings into a non-cyclic (i.e. straight or branched) chain, with the minimum number of such scissions corresponding to the number of rings defined (e.g. the term bicyclic may indicate that a minimum of two scissions would be required to convert the rings into a straight chain). For the avoidance of doubt, the term bicyclic (e.g. when employed in the context of alkyl groups) may refer to groups in which the second ring of a two-ring system is formed between two adjacent atoms of the first ring, to groups in which two non-adjacent atoms are linked by an alkyl (which, when linking two moieties, may be referred to as alkylene) group (optionally containing one or more heteroatoms), which later groups may be referred to as bridged, or to groups in which the second ring is attached to a single atom, which latter groups may be referred to as spiro compounds.

As may be used herein, the term aryl may refer to C_6-14 (e.g. C_6-10) aromatic groups. Such groups may be monocyclic or bicyclic and, when bicyclic, be either wholly or partly aromatic. C_6-10 aryl groups that may be mentioned include phenyl, naphthyl, 1,2,3,4-tetrahydronaphthyl, indanyl, and the like (e.g. phenyl, naphthyl, and the like). For the avoidance of doubt, the point of attachment of substituents on aryl groups may be via any suitable carbon atom of the ring system. For the avoidance of doubt, the skilled person will understand that aryl groups that may form part of compounds of the invention are those that are chemically obtainable, as known to those skilled in the art. Particular aryl groups that may be mentioned include phenyl. In some embodiments, any “aryl” mentioned herein refers to phenyl.

As may be used herein, references to heteroaryl (with may also be referred to as heteroaromatic) groups may refer to 5- to 14- (e.g. 5- to 10-membered heteroaromatic groups containing one or more heteroatoms (such as one or more heteroatoms selected from oxygen, nitrogen and/or sulfur). Such heteroaryl groups may comprise one, two, or three rings, of which at least one is aromatic. Certain heteroaryl groups that may be mentioned include those in which all rings forming such groups are aromatic.

Substituents on heteroaryl/heteroaromatic groups may, where appropriate, be located on any suitable atom in the ring system, including a heteroatom (e.g. on a suitable N atom). For the avoidance of doubt, the skilled person will understand that heteroaryl groups that may form part of compounds of the invention are those that are chemically obtainable, as known to those skilled in the art.

The point of attachment of heteroaryl/heteroaromatic groups may be via any atom in the ring system including (where appropriate) a heteroatom. Bicyclic heteroaryl/heteroaromatic groups may comprise a benzene ring fused to one or more further aromatic or non-aromatic heterocyclic rings, in which instances, the point of attachment of the polycyclic heteroaryl/heteroaromatic group may be via any ring including the benzene ring or the heteroaryl/heteroaromatic or heterocyclyl ring.

For the avoidance of doubt, the skilled person will understand that heteroaryl groups that may form part of compounds of the invention are those that are chemically obtainable, as known to those skilled in the art. Various heteroaryl groups will be well-known to those skilled in the art, such as pyridinyl, pyrrolyl, furanyl, thiophenyl, oxadiazolyl, thiadiazolyl, thiazolyl, oxazolyl, pyrazolyl, triazolyl, tetrazolyl, isoxazolyl, isothiazolyl, imidazolyl, imidazopyrimidinyl, imidazothiazolyl, thienothiophenyl, pyrimidinyl, furopyridinyl, indolyl, azaindolyl, pyrazinyl, pyrazolopyrimidinyl, indazolyl, quinolinyl, isoquinolinyl, quinazolinyl, benzofuranyl, benzothiophenyl, benzoimidazolyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, pyrazolopyridinyl, pyrrolopyrazolyl and purinyl.

For the avoidance of doubt, the oxides of heteroaryl/heteroaromatic groups are also embraced within the scope of the invention (e.g. the N-oxide).

As stated above, heteroaryl includes polycyclic (e.g. bicyclic) groups in which one ring is aromatic (and the other may or may not be aromatic). Hence, other heteroaryl groups that may be mentioned include groups such as benzo[1,3]dioxolyl, benzo[1,4]dioxinyl, dihydrobenzo[d]isothiazole, 3,4-dihydrobenz[1,4]oxazinyl, dihydrobenzothiophenyl, indolinyl, 5H,6H,7H-pyrrolo[1,2-b]pyrimidinyl, 1,2,3,4-tetrahydroquinolinyl, thiochromanyl, pyrazolo[3,4-b]pyridinyl, pyrrolo[3,4-c]pyrazolyl, methylenedioxyphenyl, and the like.

Particular heteroaryl groups that may be mentioned include pyrazolo[3,4-b]pyridinyl (e.g. pyrazolo[3,4-b]pyridine-5-yl), pyrrolo[3,4-c]pyrazolyl (e.g. pyrrolo[3,4-c]pyrazol-5-yl), 1,2,4 triazolyl (e.g. 1,2,4 triazol-1-yl), pyrimidinyl (e.g. pyrimidin-5-yl), pyrazolyl (e.g. pyrazol-1-yl), pyridinyl (e.g. pyridine-3-yl and pyridine-4-yl), indolyl (e.g. indol-6-yl and indol-7-yl), imidazolyl (e.g. imdazol-5-yl), isoxazolyl (e.g. isoxazol-3-yl), 1,2-methylenedioxyphenyl (e.g. 1,2-methylenedioxyphen-1-yl) and pyrazolyl (e.g. pyrazol-3-yl).

For the avoidance of doubt, where a ring is depicted having a circle therein, its presence shall indicate that the relevant ring is aromatic. Alternatively, aromatic groups may be depicted as cyclic groups comprising therein a suitable number of double bonds to allow for aromaticity.

The present invention also embraces isotopically-labelled compounds of the present invention which are identical to those recited herein, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature (or the most abundant one found in nature). All isotopes of any particular atom or element as specified herein are contemplated within the scope of the compounds of the invention. Hence, the compounds of the invention also include deuterated compounds, i.e. compounds of the invention in which one or more hydrogen atoms are replaced by the hydrogen isotope deuterium.

For the avoidance of doubt, in cases in which the identity of two or more substituents in a compound of the invention may be the same, the actual identities of the respective substituents are not in any way interdependent. For example, in the situation in which two or more R³ groups are present, those R³ groups may be the same or different. Similarly, where two or more R³ groups are present and each represent R^2a, the R^2a groups in question may be the same or different.

Also for the avoidance of doubt, when a term such as “A¹ to A⁹” is employed herein, this will be understood by the skilled person to mean A¹, A², A³, A⁴, A⁵, A⁶, A⁷, A⁸ and A⁹, inclusively. Unless otherwise stated, the same reasoning will apply to other such terms used herein.

Further for the avoidance of doubt, when it is specified that a substituent is itself optionally substituted by one or more substituents (e.g. A¹ represents aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D¹), these substituents where possible may be positioned on the same or different atoms. Such optional substituents may be present in any suitable number thereof (e.g. the relevant group may be substituted with one or more such substituents, such as one such substituent).

For the avoidance of doubt, where groups are referred to herein as being optionally substituted it is specifically contemplated that such optional substituents may be not present (i.e. references to such optional substituents may be removed), in which case the optionally substituted group may be referred to as being unsubstituted.

Where used herein, a dashed bond (i.e. “- - - ”, or the like) may indicate the position of attachment of the relevant substituent to the core molecule (i.e. the compound of the compound of formula I to which the substituent is attached).

For the avoidance of doubt, when in structures provided herein a ring is represented as having a circle therein (e.g. in the case of the ring comprising Y¹ to Y⁴ in formula I), the skilled person will understand that the relevant ring is aromatic.

For the avoidance of doubt, the skilled person will appreciate that compounds of the invention that are the subject of this invention include those that are obtainable, i.e. those that may be prepared in a stable form. That is, compounds of the invention include those that are sufficiently robust to survive isolation, e.g. from a reaction mixture, to a useful degree of purity.

In certain embodiments (i.e. certain embodiments of the first aspect of the invention) that may be mentioned, where Z³ represents N and/or (e.g. and) X² represents O, at least one R³ group is present. In certain embodiments, where Z³ represents N, at least one R³ group is present.

In further embodiments, there is the proviso that where Z³ represents N at least one R³ group is present, which proviso may be referred to herein as proviso (a).

In yet further embodiments, proviso (a) may require (in all instances) that at least one R³ group is present.

In certain embodiments, there is the proviso that the compound of formula I is not a compound selected from the following list:

• 4-(5-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl)piperidine-1-carbothioamide;
• N-(4-chlorophenyl)-4-(5-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carbothioamide;
• 4-(5-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chlorophenyl)piperidine-1-carboxamide;
• ethyl 4-{[4-(5-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carbonyl]amino}benzoate;
• 4-(5-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,6-dichloropyridin-4-yl)piperidine-1-carboxamide,which may be referred to herein as proviso (b).

In particular embodiments (i.e. particular embodiments of the first aspect of the invention), the compound of formula I is such that: X¹ and X² each represent O; or X¹ represents O and X² represents S.

Thus, in particular embodiments, X¹ represents O. For example, in certain embodiments X¹ and X² each represent O.

In particular embodiments, the compound of formula I is such that: each of Y¹ to Y⁴ independently represents CH or CR³, or Y¹ may alternatively represent N.

Preferably, Y¹, Y², Y³ and Y⁴ are not all CH. For example, in some embodiments, three of Y¹, Y², Y³ and Y⁴ are CH, and the remaining one is N or CR³; e.g. three of Y¹, Y², Y³ and Y⁴ are CH, and the remaining one is CR³.

In some further embodiments, Y¹, Y² and Y³ represent CH, or two of Y¹, Y² and Y³ represent CH, and one of Y¹, Y² and Y³ represents N; and Y⁴ represents CR³.

In some further embodiments, Y¹ and Y² represent CH, and one of Y³ and Y⁴ represents N or CR³, while the other one represents CH.

In particular embodiments, the compound of formula I is a compound of formula Ia

• • wherein:
  • Y¹ represents N, CH or CR³;
  • m represents 0 to 3; and
  • R¹ to R³, X¹, X², Z¹ to Z³, and n are as defined herein (i.e. for compounds of formula I, including all embodiments thereof).

In particular such embodiments, either

• • Y¹ represents N or CH (e.g. N) and m represents 1 to 3 (e.g. 1); or
  • Y¹ represents CR³ and m represents 0 to 3 (e.g. 0).

In certain embodiments, Y¹ represents N or CH.

In yet more particular embodiments, the compound of formula I is a compound of formula Ib

• • wherein:
  • Y¹ represents N, CH or CR³;
  • m′ represents 0 to 2; and
  • R¹ to R³, X¹, X², Z¹ to Z³, and n are as defined herein (i.e. for compounds of formula I, including all embodiments thereof).

In particular such embodiments, Y¹ represents N or CH (e.g. N) and m′ represents 1 or 2 (e.g. 1).

In certain embodiments that may be mentioned, the compound of formula I is a compound of formula Ic

• • wherein:
  • Y¹ represents N or CH; and
  • R¹ to R³, X¹, X², Z¹ to Z³, and n are as defined herein (i.e. for compounds of formula I, including all embodiments thereof).

In certain embodiments, Y¹ represents CH.

In particular embodiments, either:

• • Z¹ and Z² both represent methylene;
  • Z¹ and Z² both represent methylene linked by an additional ethylene group; or
  • Z¹ represents ethylene and Z² represents methylene.

In certain embodiments that may be mentioned, Z¹ and Z² both represent methylene.

In particular embodiments, Z³ represents CH or N. In certain embodiments, Z³ represents N.

In further embodiments, Z³ represents CH or CR. In yet further embodiments, Z³ represents CH.

Thus, in certain embodiments, the compound of formula I is a compound of formula Id

wherein R¹ to R³, X¹, X², 1 to Y⁴, Z¹ to Z³, and n are as defined herein (i.e. for compounds of formula I, including all embodiments thereof).

In further embodiments, the compound of formula I is a compound of formula Ie

wherein R¹ to R³, X¹, X², Y¹ to Y⁴, and Z¹ to Z³ are as defined herein (i.e. for compounds of formula I, including all embodiments thereof), and n′ represents 0 to 12, as appropriate.

In yet further embodiments, the compound of formula I is a compound of formula If

wherein R¹ to R³, X¹, X², Y¹ to Y⁴, and Z¹ to Z³ are as defined herein (i.e. for compounds of formula I, including all embodiments thereof), and n″ represents 0 to 10.

In yet further embodiments, the compound of formula I is a compound of formula Ig

wherein R¹ to R³, X¹, X², Y¹ to Y⁴, and Z¹ to Z³ are as defined herein (i.e. for compounds of formula I, including all embodiments thereof), and n″ represents 0 to 10.

For the avoidance of doubt, the skilled person will understand that the stereochemistry shown in formula Ig is relative, thus showing that the substituents on the cyclohexane are in the cis configuration. In such instances, compounds may be defined as being provided such that the required diastereoisomer is present in an excess when compared to the relative amounts of other possible diastereoisomers, such as being present in a diastereomeric excess (d.e.) of at least 60% (such as at least 70%, 80%, 85%, 90% or 95%, e.g. at least 99% or at least 99.9%).

In particular embodiments, n (and, similarly, n′ and n″) represents 0 or 1.

In particular embodiments, each R¹ independently represents, where possible: halo, oxy, —NO₂, —CN, —R^1a, —OR^1b, —S(O)_qR^1c, —S(O)_r(R^1d)(R^1e), —N(R^1f)S(O)_sR^1g, —N(R^1h)(R¹ⁱ), —C(O)OR^1j, or —C(O)NR^1kR^1l. In more particular embodiments, each R¹ independently represents halo (e.g. fluoro), —R^1a or —OR^1b. In yet more particular embodiments, each R¹ independently represents —R^1a or —OR^1b, such as wherein R^1a represents C_1-6 alkyl (e.g. methyl); and R^1b represents H. In more particular embodiments, each R¹ independently represents fluoro, methyl or hydroxy, e.g. fluoro or methyl, in particular fluoro.

In particular embodiments, where n represents 1, the R¹ group is present in a position that is alpha or beta to the point of attachment of the ring on which such groups are present to the essential benzimidazole ring.

In certain embodiments, n represents 0.

In a compound of formula I, R² represents

• • (i) phenyl optionally substituted by one or more (e.g. 1-3, or 1-2) groups independently selected from A⁴, (“option a(i)”)
  • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more (e.g. 1-3, or 1-2) groups selected from oxy and A⁵ (“option a(ii)”), or
  • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more (e.g. 1-3, or 1-2) groups selected from oxy and A⁶ (“option a(iii)”)

In some embodiments, R² represents option a(i) or option a(ii). In some embodiments, R² represents option a(i) or option a(iii). In some embodiments, R² represents option a(ii) or option a(iii).

In some embodiments, R² represents option a(i). In some embodiments, R² represents option a(ii). In some embodiments, R² represents option a(iii).

For the avoidance of doubt, it is pointed out that, for example, the indication that “R² represents option a(i)” is equivalent to an indication that “R² represents (i) phenyl optionally substituted by one or more (e.g. 1-3, or 1-2) groups independently selected from A⁴”, and consequently these two types of expression may replace each other herein.

In some embodiments, in option a(i) the phenyl is substituted by one or two groups independently selected from A⁴. (For the avoidance of doubt, it is pointed out that this means that, in some embodiments, when R² represents option a(i), R² more particularly represents phenyl substituted by one or two groups independently selected from A⁴).

In some embodiments, in option a(i) the phenyl is substituted by one group independently selected from A⁴.

In some embodiments, in option a(i), one A⁴ in the meta position relative to the point of attachment to the essential amide group, e.g. the phenyl is substituted by one group independently selected from A⁴, which is in meta position on the phenyl ring.

In some further embodiments, in option a(i), one A⁴ in the para position relative to the point of attachment to the essential amide group.

In some embodiments, in option a(i), the phenyl is substituted by at least 2 groups independently selected from A⁴, (in particular 2 or 3 groups, e.g. 2 groups), of which one group is in the para position relative to the point of attachment of the phenyl ring to the essential amide group, and one is in the meta position relative to the point of attachment of the phenyl ring to the essential amide group. Thus, in some embodiments, the compound of formula I is as represented by formula Ih

wherein each R¹, n X¹, X², Y¹ to Y⁴, Z¹ to Z³, each A⁴, and n are as defined herein, and z is an integer of from 0 to 2, e.g. z is 0 or 1. In some embodiments, z is 0. In some other embodiments, z is 1. In some particular embodiments, when z is 1, the compound of formula I is as represented by formula Ii

wherein X¹, X², Y¹ to Y⁴, Z¹ to Z³, and each A⁴, and n are as defined herein.

In some embodiments, R² cannot be unsubstituted phenyl, i.e. in option a(i), the phenyl is substituted by at least one group A⁴.

In some preferred embodiments, the compound of formula I is as illustrated by formula Ij

wherein R¹, R², R³ and n are as defined herein. In some of these embodiments, n is 0, i.e. the compound more particularly is as represented by formula Ik

wherein R² and R³ are as represented herein.

In some of these preferred embodiments, the compound of formula Ik is also a compound of formula Ih, i.e. a compound as represented by formula Im

wherein R³, each A⁴ and z are as defined herein, e.g. z is 0 or 1. In some embodiments, z is 0. In some other particular embodiments, z is 1. In some of these embodiments, the compound is as represented by formula In

wherein R³ and each A⁴ are as defined herein.

In some embodiments, in option a(i), R² represents a moiety selected from 3-(dimethylamino)phenyl, 3-(hydroxymethyl)phenyl, 3-(trifluoromethyl)phenyl, 3-aminophenyl, 3-chlorophenyl, 3-hydroxyphenyl, 3-methoxyphenyl, 3-methylphenyl, 4-chlorophenyl, 4-(dimethylamino)phenyl, 4-(trifluoromethyl)phenyl, 4-carbamoylphenyl, 4-cyanophenyl, 4-ethylphenyl, 4-fluorophenyl, 4-hydroxyphenyl, 4-iodophenyl, 4-methoxyphenyl, 4-methylphenyl, 2,3-dimethylphenyl, 2,4-dichlorophenyl, 2-fluoro-4-methoxyphenyl, 2-fluoro-4-methylphenyl, 2-hydroxy-4-methylphenyl, 3,4-dichlorophenyl, 3,4-difluorophenyl, 3,4-dimethoxyphenyl, 3,4-dimethylphenyl, 3-chloro-4-(trifluoromethoxy)phenyl, 3-chloro-4-cyanophenyl, 3-chloro-4-fluorophenyl, 3-chloro-4-hydroxyphenyl, 3-chloro-4-iodophenyl, 3-chloro-4-methoxyphenyl, 3-chloro-5-methoxyphenyl, 3-cyano-4-methoxyphenyl, 3-fluoro-4-(trifluoromethyl)phenyl, 3-fluoro-4-methoxyphenyl, 3-fluoro-5-methoxyphenyl, 3-hydroxy-4-methylphenyl, 3-methoxy-4-methylphenyl, 3-methoxy-5-(trifluoromethyl)phenyl, 4-bromo-3-chlorophenyl, 4-bromo-3-methylphenyl, 4-chloro-3-(trifluoromethyl)phenyl, 4-chloro-3-cyanophenyl, 4-chloro-3-fluorophenyl, 4-chloro-3-methoxyphenyl, 4-chloro-3-methylphenyl, 4-cyano-3-methoxyphenyl, 4-fluoro-3-methoxyphenyl, 4-fluoro-3-methylphenyl, 4-hydroxy-3-methylphenyl, 4-iodo-3-methylphenyl, 4-methoxy-3-(methoxycarbonyl)phenyl, 4-methoxy-3-(trifluoromethyl)phenyl, 4-methoxy-3-methylphenyl, 4-methyl-3-(trifluoromethyl)phenyl, 2-amino-4,5-dimethylphenyl, 2,3-difluoro-4-methoxyphenyl, 3,4,5-trimethoxyphenyl, and 3,5-difluoro-4-methoxyphenyl. In some embodiments, e.g. of a compound of formula Ig, R₂ is 3-methoxy-4-methylphenyl.

In some embodiments, in option a(ii), the 5- or 6-membered monocyclic heteroaryl is unsubstituted or substituted by 1, 2 or 3 (in particular 1 or 2, more particularly 1) group(s) A⁵. In some embodiments, in option a(ii), the 5- or 6-membered monocyclic heteroaryl is unsubstituted, i.e. carries no group A⁵. In some other embodiments, in option a(ii), the 5- or 6-membered monocyclic heteroaryl substituted by 1, 2 or 3 (in particular 1 or 2, more particularly 1) group(s) A⁵.

In some embodiments, in option a(ii), the 5- or 6-membered monocyclic heteroaryl more particularly is 6-membered monocyclic heteroaryl. In some other embodiments, in option a(ii), the 5- or 6-membered monocyclic heteroaryl more particularly is 5-membered monocyclic heteroaryl. In some embodiments, in option a(ii), the monocyclic heteroraryl, when 5-membered, contains 1-3, or 1-2, or 1, heteroatom(s) selected from N, O and S, e.g. from N and O. In some embodiments, in option a(ii), the monocyclic heteroraryl, when 6-membered, contains 1 or 2 nitrogen atoms.

In some embodiments, in option a(ii), the heteroaryl is selected from imidazolyl, pyrazolyl, oxazolyl, and pyridinyl. In some particular embodiments, the heteroraryl is pyridinyl, e.g. pyridin-2-yl or pyridin-3-yl, in particular pyridin-3-yl.

In some embodiments, when in option a(ii) the heteroaryl is pyridin-2-yl or pyridin-3-yl, in particular pyridin-3-yl, said pyridinyl is substituted in para position relative to the point of attachment of the pyridinyl ring to the essential amide group. In some of these embodiments, the pyridinyl is substituted with one group A⁵. In some other embodiments, the pyridinyl is substituted with two groups A⁵, one of which is in para position, and the other one of which is in meta position, relative to the point of attachment of the pyridinyl ring to the essential amide group.

In some embodiments, in option a(ii), R² represents a moiety selected from 5-chloropyridin-3-yl, 5-methylpyridin-2-yl, 6-chloropyridin-3-yl, 6-methoxypyridin-3-yl, 6-methylpyridin-3-yl, 5,6-dichloropyridin-3-yl, 5-chloro-6-methoxypyridin-3-yl, 5-chloro-6-methylpyridin-2-yl, 6-chloro-5-methylpyridin-3-yl, and 6-methoxy-5-methylpyridin-3-yl.

In some embodiments, in option a(iii), the bicyclic heteroaryl is unsubstituted, i.e. carries no group A⁶. In some other embodiments, in option a(iii), the bicyclic heteroaryl is substituted by one or more (e.g. 1-3) groups selected from A⁶, e.g. 1, 2 or 3 groups selected from A⁶, or 1 or 2 groups selected from A⁶, e.g. one group A⁶. In some embodiments, the bicyclic heteroaryl is unsubstituted or substituted by one group A⁶. In option a(iii), the bicyclic heteroaryl contains one benzene ring fused to a heterocyclic ring, e.g. a 5- or 6-membered heterocyclic ring, which may be saturated or unsaturated and aromatic or non-aromatic, and contain one or more heteroatoms, e.g. 1 or 2 heteroatoms. In some embodiments, the heterocyclic ring is 5- or 6-membered and aromatic, e.g. 5- or 6-membered and aromatic and containing 1 or 2 heteroatoms selected from N, O and S, e.g. from N and O.

It should be pointed out that the bicyclic heteroaryl may be attached to the essential amide group by a bond to either the benzene ring or the heterocyclic ring. In some embodiments, the bicyclic heteroaryl is attached to the essential amide group by a bond to the benzene ring of the bicyclic heteroaryl.

In some embodiments, in option a(iii), the bicyclic heteroaryl is selected from benzodioxolyl, benzodioxinyl, indolyl, indazolyl, benzoxazolyl, quinolinyl, and benzodiazolyl. In some of these embodiments, the bicyclic heteroaryl more particularly is indolyl, indazolyl, benzoxazolyl, quinolinyl, or benzodiazolyl.

In some particular embodiments, in option a(iii), R² represents a moiety selected from 1H-indolyl, 1H-indolyl, 1H-indazolyl, 1H-indazolyl, 1-methyl-1H-indazolyl, 3-methyl-1H-indazolyl, 1-methyl-1H-1,3-benzodiazolyl, 2-methyl-1,3-benzoxazolyl, quinolinyl, 2,3-dihydro-1,4-benzodioxinyl, and 2H-1,3-benzodioxolyl; e.g. from 1H-indol-4-yl, 1H-indol-5-yl, 1H-indazol-6-yl, 1H-indazol-7-yl, 1-methyl-1H-indazol-5-yl, 3-methyl-1H-indazol-5-yl, 1-methyl-1H-1,3-benzodiazol-2-yl, 2-methyl-1,3-benzoxazol-6-yl, quinolin-6-yl, 2,3-dihydro-1,4-benzodioxin-6-yl, and 2H-1,3-benzodioxol-5-yl.

In a compound of formula I, each R³ independently represents

• • (i) halo, —NO₂, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —S(O)_rN(R^2d)(R^2e), —N(R^2f)S(O)_sR^2g, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l (“option b(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁷ (“option b(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from A³, (“option b(ii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁹ (“option b(iv)”).

In some embodiments, R³ represents option b(i), option b(ii) or option b(iii). In some embodiments, R³ represents option b(i) or option b(iv). In some embodiments, R³ represents option b(i), option b(ii), or option b(iv). In some embodiments, R³ represents option b(i), option b(ii), or option b(iv).

In some particular embodiments, R³ represents option b(i). In some other particular embodiments, R³ represents option b(ii). In still other embodiments, R³ represents option b(iii). In some further embodiments, R³ represents option b(iv).

In some embodiments, in option b(i), R³ more particularly represents a moiety selected from halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR^2j, and —C(O)NR^2kR^2l. In some further embodiments, in option b(i), the moiety is selected from halo, CN, —R^2a, —OR^2b, —N(R^2h)(R²ⁱ), —C(O)OR^2j, and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from halo, —OR^2b, N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from halo, —N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from halo.

In still some further embodiments, in option b(i), the moiety is selected from —OR^2b, —N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from —N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —N(R^2h)(R²ⁱ).

In still some further embodiments, in option b(i), the moiety is —OR^2b or —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —OR^2b.

In still some further embodiments, in option b(i), the moiety is selected from halo, —R^2a, —OR^2b, N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from halo, —R^2a, N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from halo and —R^2a.

In still some further embodiments, in option b(i), the moiety is selected from —R^2a, —OR^2b, —N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is selected from —R^2a, N(R^2h)(R²ⁱ), and —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —R^2a or —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —R^2a or —N(R^2h)(R²ⁱ). In still some further embodiments, in option b(i), the moiety is —R^2a, —OR^2b or —C(O)NR^2kR^2l. In still some further embodiments, in option b(i), the moiety is —R^2a or —OR^2b. In still some further embodiments, in option b(i), the moiety is —R^2a.

In some embodiments, in option b(i), the moiety —S(O)_qR^2c more particularly is a moiety selected from —S(O)₂R^2c and —SR^2c. In some embodiments, the moiety —S(O)_qR^2c is —SR^2c. In some other embodiments, the moiety —S(O)_qR^2c is —S(O)R^2c or —S(O)₂R^2c, in particular —S(O)₂R^2c.

In certain embodiments, each R³ independently represents halo (e.g. F or Br, such as Br).

In further embodiments, where Z³ represents CH or CR¹, each R³ represents F (such as wherein one R³ group is present).

In some embodiments, in option b(ii), R³ represents phenyl optionally substituted by one or more (e.g. 1-3) groups independently selected from A⁷. In some of these embodiments, the phenyl is substituted by 1-3 groups independently selected from A⁷, e.g. 1 or 2 groups independently selected from A⁷, or one group independently selected from A⁷.

In some particular embodiments, in option b(ii), R³ represents a moiety selected from 2-aminophenyl, 2-((dimethylamino)methyl)phenyl, 3-aminophenyl, 3-((2-methoxyethyl)carbamoyl)phenyl, 3-(2-(dimethylamino)ethoxy)phenyl, 3-(aminomethyl)phenyl, 3-(carbamoylmethyl)phenyl, 3-(methoxycarbonyl)phenyl, 3-(morpholine-4-carbonyl)phenyl, 3,5-bis(trifluoromethyl)phenyl, 3-[2-(dimethylamino)ethoxy]phenyl, 3-carboxyphenyl, 3-fluorophenyl, 4-(2-(dimethylamino)ethoxy)phenyl, 4-(2,2,2-trifluoroacetyl)phenyl, 4-(aminomethyl)phenyl, 4-carboxyphenyl, and 4-sulfamoylphenyl.

In option b(iii), the heteroaryl is optionally substituted by one or more (e.g. 1, 2 or 3) groups selected from A⁸, in particular by 1 or 2 groups selected from A⁸. In some embodiments, in option b(iii), the heteroaryl is unsubstituted or substituted by one group A⁸.

In option b(iii), the required heteroaryl is as generally described herein above. For example, the heteroaryl may be monocyclic and 5- or 6-membered and contain one or more (e.g. 1, 2 or 3) heteroatoms selected from N, O and S; or bicyclic and 8- to 10-membered (or 9- or 10-membered) and contain one or more (e.g. 1, 2, 3 or 4) heteroatoms selected from N, O and S. For example, the heteroaryl may be selected from 1H-pyrrolyl, 1H-pyrazolyl, triazolyl (such as 1H-1,2,4-triazolyl) pyridinyl, pyrimidinyl, 1H-pyrazolopyridinyl (e.g. 1H-pyrazolo[3,4-b]pyridinyl, and 1H,4H,5H,6H-pyrrolopyrazolyl, (e.g. 1H,4H,5H,6H-pyrrolo[3,4-c]pyrazolyl).

In some embodiments, in option b(iii), R³ represents a moiety selected from 1H-pyrrol-2-yl, 1H-pyrazol-1-yl, 4-bromo-1H-pyrazol-1-yl, 4-(ethylcarbamoyl)-1H-pyrazol-1-yl, 4-(diethylcarbamoyl)-1H-pyrazol-1-yl, 4-(2-(dimethylamino)ethyl)carbamoyl)-1H-pyrazol-1-yl, 4-((2,3-dihydroxypropyl)carbamoyl)-1H-pyrazol-1-yl, 1H-1,2,4-triazol-1-yl, pyridin-3-yl, pyridin-4-yl, 2-ethoxypyridin-3-yl, 2-(trifluoromethyl)pyridin-4-yl, pyridin-4-yl, 5-aminopyridin-3-yl, 6-aminopyridin-3-yl, 6-(hydroxymethyl)pyridin-3-yl, 6-methoxypyridin-3-yl, pyrimidin-5-yl, 1H-pyrazolo[3,4-b]pyridin-5-yl, and 1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl.

In option b(iv), the heterocyclyl is optionally substituted by one or more (e.g. 1-3, or 1-2) groups selected from A⁹, in particular by 1 or 2 groups selected from A⁹, e.g. 1 group selected from A⁹. In some embodiments, in option b(iv), the heterocyclyl is unsubstituted or substituted by one group A⁹.

In option b(iv), the heterocyclyl is a ring as generally described herein. For example, the heterocyclyl may be a monocyclic, saturated or unsaturated (non-aromatic) 4- to 8-membered, more particularly 4- to 6-membered (e.g. 5- or 6-membered) ring containing 1, 2 or 3 (e.g. 1 or 2) heteroatoms selected from N, O and S. In some embodiments, the heterocyclyl is 5- or 6-membered and contains 1 or 2 heteroatoms selected from N, O and S, in particular N or O. In some embodiments, said heterocyclyl contains at least one N in the ring. In some of these embodiments, the heterocyclyl containing at least one N in the ring is attached to the benzene ring of the compound of formula I by a bond to said N.

In some embodiments, in option b(iv), the heterocyclyl is selected from pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, and 1,2,3,6-tetrahydropyridinyl; e.g. from pyrrolidin-1-yl, piperidin-1-yl, piperazin-1-yl, morpholin-4-yl, and 1,2,3,6-tetrahydropyridin-4-yl.

In some particular embodiments, in option b(iv), R³ represents a moiety selected from pyrrolidin-1-yl, 3-aminopyrrolidin-1-yl, 3-(dimethylamino)pyrrolidin-1-yl, 3-acetamidopyrrolidin-1-yl, 3-((tert-butoxycarbonyl)amino)pyrrolidin-1-yl, piperazin-1-yl, 4-aminopiperidin-1-yl, 1,2,3,6-tetrahydropyridin-4-yl, 1-methyl-1,2,3,6-tetrahydropyridin-4-yl, and morpholin-4-yl.

In a compound of formula I, each R^2a represents:

• • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B¹ (“option c(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B² (“option c(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and B³ (“option c(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B⁴ (“option c(iv)”); and
  • each R^2b to R^2l independently represents H, or
  • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B¹ (“option d(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B² (“option d(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and B³ (“option d(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B⁴ (“option d(iv)”).

In some embodiments, each R^2a represents option c(i), option c(iii), or option c(iv), and each R^2b to R^2l independently represents H, option d(i), option d(iii) or option d(iv). In some embodiments, each R^2a represents option c(i) or option c(iv), and each R^2b to R^2l independently represents H, option d(i) or option d(iv). In some further embodiments, each R^2a represents option c(i) and each R^2b to R^2l independently represents H or option d(i).

In some embodiments, in any one of R^2a to R^2l, any C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl more particularly is (saturated) C_1-6 alkyl, e.g. C_1-4alkyl, or C_1-3alkyl (including linear and, when there are a sufficient number of carbon atoms, branched alkyl and cycloalkyl).

In some of the above embodiments, when any one of R^2a to R^2l represents (optionally substituted) C_1-6alkyl, C_2-6alkenyl, or C_2-6 alkynyl, any such alkyl, alkynyl or alkenyl more particularly is C_1-4 alkyl, any C_2-6 alkenyl more particularly is C_2-4 alkenyl, and any C_2-6 alkynyl more particularly is C_2-4 alkynyl. In some further of the above embodiments, any such alkyl more particularly is C_1-3 alkyl, any such alkenyl more particularly is C_2-3 alkenyl, and any such alkynyl more particularly is C_2-3 alkynyl.

When any one of R^2a to R^2l represents (optionally substituted) aryl, such aryl preferably is phenyl.

When any one of R^2a to R^2l represents (optionally substituted) heteroaryl, such heteroaryl is as defined herein above, e.g. it may be 5- or 6-membered and contain from 1 to 3 heteroatoms, such as 1 to 3 heteroatoms selected from N, O and S, in particular from N and O.

When any one of any one of R^2a to R^2l represents (optionally substituted) heterocyclyl, such heterocyclyl is as defined herein above, and e.g. may be selected from 4- to 6-membered heterocyclyl containing one or more heteroatoms selected from N, O and S, e.g. 1 or 3 heteroatoms selected from N, O and S, e.g. from N and O. For example, the heterocyclyl may be selected from piperazinyl, morpholinyl, piperidinyl, pyrrolidinyl, and azetidinyl.

In particular embodiments:

• • R^2a represents C_1-6 alkyl (e.g. C_1-3 alkyl) optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B¹;
  • R^2b represents H or C_1-6 alkyl (e.g. C_1-2 alkyl);
  • R^2c represents H or C_1-6 alkyl (e.g. C₁ alkyl), such as C_1-6 alkyl (e.g. C₁ alkyl); and
  • R^2h and R²ⁱ independently represent H or C_1-6 alkyl (e.g. C₁ alkyl).

In some embodiments, R^2a represents C_1-6 alkyl, e.g. C_1-3 alkyl, such as methyl, ethyl, propyl or cyclopropyl; or R^2a represents C_1-6 alkyl (e.g. C_1-3 alkyl, such as methyl, ethyl, propyl or cyclopropyl), substituted by one or more moieties selected from oxy and B¹, e.g. one oxy and/or 1, 2 or 3 moieties B.

In some embodiments, R^2a represents C_1-6 alkyl (e.g. C_1-3 alkyl, such as methyl, ethyl, propyl or cyclopropyl), said alkyl being substituted by one or more moieties selected from oxy and B¹, e.g. one oxy and/or 1, 2 or 3 moieties B¹, or said alkyl being substituted by one or more (e.g. 1, 2 or 3) moieties B.

In some embodiments, when R^2a represents C_1-6 alkyl (e.g. C_1-3 alkyl, such as methyl, ethyl, propyl or cyclopropyl) substituted by one or more moieties B¹, such moieties are selected from halogen (e.g. fluoro), —OR^4b, —N(R^4h)(R⁴ⁱ) and —(O)OR^4j, e.g. from OH, NH₂, and methoxycarbonyl.

In some embodiments, when R^2a represents C_1-6 alkyl substituted by one or more moieties selected from oxy and B¹, R^2a more particularly represents —C(O)B¹, wherein B¹ is as described herein. For example, in some embodiments, in —C(O)B¹, B¹ represents heterocyclyl as described herein (e.g. 4- to 8 membered heterocyclyl, or 4- to 6-membered heterocyclyl, e.g. heterocyclyl containing 1 or 2 heteroatoms) optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶, said heterocyclyl containing at least one nitrogen atom in the ring, and said heterocyclyl being attached to the C(O) moiety by a bond to said nitrogen atom. In some of these embodiments, the heterocyclyl is selected from pyrrolidinyl, piperidinyl, piperazinyl, and morpholinyl.

In some embodiments, when R^2a represents a moiety —C(O)B¹, said moiety is selected from 3-(dimethylamino)pyrrolidine-1-carbonyl, 2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl, 2-carbamoylpyrrolidine-1-carbonyl, 4-(dimethylamino)piperidine-1-carbonyl, piperazine-1-carbonyl, 4-methylpiperazine-1-carbonyl, 3-(trifluoromethyl)piperazine-1-carbonyl, 4-(2-(dimethylamino)ethyl)piperazine-1-carbonyl, or morpholine-4-carbonyl.

In some embodiments, R^2a represents a moiety selected from methyl, 2-methoxy-2-oxoethyl, 2-hydroxyethyl, cyclopropyl, aminomethyl, 3-(dimethylamino)pyrrolidine-1-carbonyl, 2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl, 2-carbamoylpyrrolidine-1-carbonyl, 4-(dimethylamino)piperidine-1-carbonyl, piperazine-1-carbonyl, 4-methylpiperazine-1-carbonyl, 3-(trifluoromethyl)piperazine-1-carbonyl, 4-(2-(dimethylamino)ethyl)piperazine-1-carbonyl, and morpholine-4-carbonyl.

In the moiety —OR^2b, R^2b is as defined herein above. In some particular embodiments, R^2b represents a moiety selected from H and C_1-6 alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, or R^2b represents a heterocyclyl as defined herein.

In some embodiments, R^2b is as defined herein, but does not represent H.

When R^2b represents an alkyl substituted by one or more (e.g. one) B¹, each B¹ is as defined herein. In some embodiments, each B¹, when part of R^2b, independently represents a moiety selected from halo (e.g. F), —OR^4b, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, and —C(O)NR^4kR^4l; e.g. from halo (e.g. F), —OR^4b, —N(R^4h)(R⁴ⁱ) and —C(O)OR^4j; in particular from —OR^4b and —N(R^4h)(R⁴ⁱ).

In the moiety —S(O)_qR^2c, R^2c is as defined herein above. In some embodiments, R^2c represents a moiety selected from H and C_1-6 alkyl (e.g. H and C_1-3 alkyl, or H and C₁ alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, as defined herein. In some embodiments, R^2c represents H, methyl, (4-methoxyphenyl)methyl, or carboxymethyl, in particular H or methyl, e.g. H. In still other embodiments, R^2c is as defined herein, but does not represent H; e.g. R^2c represents a moiety selected from C_1-6 alkyl (e.g. C_1-3 alkyl, or C₁ alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, as defined herein.

In the moiety —N(R^2h)(R²ⁱ), each one of R^2h and R²ⁱ is as defined herein above. In some embodiments, R^2h represents H or C_1-6 alkyl, e.g. H or C_1-3 alkyl, or H or C_1-2 alkyl, e.g. H or methyl, and R²ⁱ is as defined herein. In some embodiments, R²ⁱ is as defined herein, but does not represent H.

In some embodiments, R²ⁱ represents H, C_1-6alkyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B, heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and B³ (in particular from B³), and heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B⁴ (in particular from B⁴).

In some of these embodiment, each B¹, when part of R²ⁱ, independently represents a moiety selected from halo, —OR^4b, —N(R^4h)(R⁴ⁱ), —C(O)NR^4kR^4l, heteroaryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁵, and heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁶.

In some further of these embodiment, each such B¹ independently represents a moiety selected from halo, —OR^4b, —N(R^4h)(R⁴ⁱ), heteroaryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁵, and heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁶.

In some embodiments, when R²ⁱ represents C_1-6 alkyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and B, R²ⁱ more particularly represents C_1-6 alkyl substituted by one oxy and optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹. In some of these embodiments, R²ⁱ represents:

• • (a) —C(O)C_1-6 alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, wherein B¹ is as defined herein, or
  • (b) —C(O)B¹, wherein the B¹ attached to the C(O) is as defined herein, e.g. said B¹ represents:
  • aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁴,
  • heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶.

In some more particular embodiments, R²ⁱ represents:

• • (a) —C(O)C_1-3 alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, wherein B¹ is as defined herein, or
  • (b) —C(O)B¹, wherein the B¹ attached to the C(O) is as defined herein, e.g. said B¹ represents:
  • aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁴,
  • heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶.

In some of the above embodiments, R²ⁱ represents —C(O)C_1-3 alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from B¹, wherein B¹ is as defined herein.

In some of the above embodiments, R²ⁱ represents —C(O)B¹, wherein the B¹ attached to the C(O) represents:

• • aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁴,
  • heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶.

In some of the above embodiments, when R²ⁱ represents —C(O)B¹, the B¹ attached to the C(O) represents heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶.

In some of the above embodiments, when R²ⁱ represents —C(O)B¹, the B¹ attached to the C(O) represents heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶.

In some of the above embodiments, when R²ⁱ represents —C(O)B′, the B¹ attached to the C(O) represents heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵.

In some embodiments, R²ⁱ represents a moiety selected from H, methyl, ethyl, propyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, benzyl, pyrimidin-2-yl, 1-methylpyrrolidin-3-yl, 2-aminoethyl, 3-aminopropyl, 2-(methylamino)ethyl, 2-(dimethylamino)ethyl, 3-((tert-butoxycarbonyl)amino)propyl, acetyl, 2-methoxyacetyl, 2-aminoacetyl, 2-(dimethylamino)acetyl, 3-aminopropanoyl, 2-morpholinoacetyl, morpholine-2-carbonyl, 4-hydroxypyrrolidine-2-carbonyl, azetidine-2-carbonyl, 1H-pyrazole-3-carbonyl, 1-methyl-1H-pyrazole-5-carbonyl, oxazole-5-carbonyl, 2-aminooxazole-4-carbonyl, 5-methylisoxazole-3-carbonyl, 1-methyl-1H-imidazole-2-carbonyl, and 1-methyl-1H-imidazole-4-carbonyl.

In some of the above embodiments, R^2h represents H or methyl, in particular H.

In the moiety —C(O)N(R^2k)(R²ⁱ) each one of R^2k and R²ⁱ is as defined herein above. In some embodiments, R^2k represents H or C_1-6 alkyl, e.g. H or C_1-3 alkyl, or H or C_1-2 alkyl, e.g. H or methyl, in particular H; and R²ⁱ is as defined herein. In some embodiments, R^2l does not represent H.

In some embodiments, R^2l represents H, C_1-6 alkyl optionally substituted by one or more B, heteroaryl optionally substituted by one or more groups selected from B³, or heterocyclyl optionally substituted by one or more groups independently selected from B⁴. In some of these embodiments, any B¹, when part of R^2l, represents a moiety selected from —OR^4a, —N(R^4h)(R⁴ⁱ), —C(O)NR^4kR^4l, heteroaryl optionally substituted by one or more groups selected from D⁵, and heterocyclyl optionally substituted by one or more groups independently selected from D⁶. For example, in some embodiments, any such B¹ represents a moiety selected from hydroxy, amino, methylamino, dimethylamino, acetamido, carbamoyl, methylsulfonamido, pyrrolidinyl (e.g. pyrrolidin-2-yl), piperazinyl (e.g. piperazin-1-yl), morpholinyl (e.g. morpholin-3-yl, or morpholin-4-yl), oxolanyl (e.g. oxolan-2-yl), 1H-imidazol-2-yl (e.g. 1H-imidazol-2-yl), and pyrimidinyl (e.g. pyrimidin-2-yl).

In some particular embodiments, R^2k represents a moiety selected from H, methyl, 2-hydroxyethyl, 2-aminoethyl, 2-(dimethylamino)ethyl, 2-(methylamino)ethyl, 3-aminopropyl, 2-acetamidoethyl, 2,3-dihydroxypropyl, 2-(methylsulfonamido)ethyl, 3-amino-3-oxopropyl, (pyrrolidin-2-yl)methyl, 2-(piperazin-1-yl)ethyl, 2-(morpholin-4-yl)ethyl, (oxolan-2-yl)methyl, (1H-imidazol-2-yl)methyl, pyrimidin-2-yl)methyl, (morpholin-3-yl)methyl, azetidin-3-yl, pyrrolidin-3-yl, and 1-methylpyrrolidin-3-yl.

In a compound of formula I, each one of A¹ to A⁹ independently represents

• • (i) halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ)—C(O)OR^3j, or —C(O)NR^3kR^3l (“option e(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D¹ (“option e(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and D² (“option e(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D³ (“option e(iv)”).

In some embodiments, each A¹ to A⁹ independently represents option e(i) or option e(iv). In some embodiments, each A¹ to A⁹ independently represents option e(i).

In some embodiments, A¹, A² and A³ are absent, and each one of A⁴ to A⁹ is as defined herein above.

In some embodiments, in option e(i), each A¹ to A⁹ (e.g. A⁴ to A⁹) independently represents a moiety selected from halo, —CN, —R^3a, —OR^3b, —S(O)_rN(R^3d)(R^3e), —N(R^3h)(R^3l), —C(O)OR^3j, and —C(O)NR^3kR^3l. In some further embodiments, in option e(i), each such moiety is selected from halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)C(O)OR^3j, and —C(O)NR^3kR^3l. In some further embodiments, in option e(i) each such moiety is selected from halo, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l.

Particular A⁴ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l More particular A⁴ groups that may be mentioned include halo (e.g. Cl, F, Br and I), —CN, —R^3a, —OR^3b, and —C(O)OR³. For example, A⁴ may represent halo (e.g. I).

In some embodiments, any A⁴ group represents a moiety selected from halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)C(O)OR^3j, and —C(O)NR^3kR^3l; e.g. from halo, —CN, —R^3a, —OR^3b, and —N(R^3h)(R³ⁱ).

In some embodiments, any A⁴ group represents a moiety selected from halo, —R^3a, and —OR^3b, e.g. from halo, C_1-6 alkyl, and C_1-6alkoxy, such as from halo, C_1-3 alkyl, and C_1-3 alkoxy, in particular halo, methyl and methoxy, e.g. halo.

In some embodiments, any A⁴ group represents a moiety selected from halo, and —R^3a e.g. from halo, and C_1-6 alkyl, such as from halo, and C_1-3 alkyl, in particular halo, and methyl.

In some embodiments, any A⁴ group represents a moiety selected from —R^3a, and —OR^3b, e.g. from C_1-6 alkyl, and C_1-6 alkoxy, such as from C_1-3 alkyl, and C_1-3 alkoxy, in particular methyl and methoxy.

In some embodiments, any A⁴ group represents —OR^3b, e.g. C_1-6 alkoxy, or C_1-3 alkoxy, in particular methoxy. In some other embodiments, any A⁴ group represents a moiety selected from —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)—C(O)OR^3j, and —C(O)NR^3kR^3l; e.g. from —CN, —R^3a, —OR^3b, and —N(R^3h)(R³ⁱ); or from —R^3a, —OR^3b, —N(R^3h)(R³ⁱ) and —C(O)OR^3j; in particular from —R^3a, —OR^3b, and —N(R^3h)(R³ⁱ). In some particular embodiments, any A⁴ group represents a moiety selected from R^3a, and —OR^3b; e.g. methyl and methoxy.

In some embodiments, when A⁴ is or comprises an alkyl group (such as A⁴ being methyl or methoxy), such alkyl group may be substituted by one or more halo, e.g. one or more fluoro, such as in trifluoromethyl or trifluoromethoxy. Thus, in some embodiments, A⁴ may represent a moiety selected from halo, methyl, trifluoromethyl, methoxy and trifluoromethoxy, e.g. from methyl, trifluoromethyl, methoxy and trifluoromethoxy.

In some embodiments, when any A⁴ is halo, such halo more particularly is selected from chloro, bromo and iodo, e.g. chloro and iodo. In some embodiments, when any A⁴ is halo, such halo is iodo. In some embodiments, when any A⁴ is halo, such halo is chloro.

Particular A⁵ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), and —C(O)NR^3kR^3l. More particular A⁵ groups that may be mentioned include halo (e.g. Cl) —R^3a (e.g. methyl) and —OR^3b (e.g. —OMe).

Particular A⁶ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l More particular A⁶ groups that may be mentioned include halo (e.g. Cl) —R^3a (e.g. methyl) and —OR^3b (e.g. —OMe). More particular A⁶ groups that may be mentioned include —R^3a.

Particular A⁷ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d) (R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l. More particular A⁷ groups that may be mentioned include halo (e.g. F), —R^3a, —OR^3b, —S(O)₂N(R^3d)(R^3e), —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l.

Particular A⁸ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l More particular A⁸ groups that may be mentioned include halo (e.g. Br), —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)—C(O)OR^3j, and —C(O)NR^3kR^3l; e.g. halo (e.g. Br), —R^3a, —OR^3b, —N(R^3h)(R³ⁱ), and —C(O)NR^3kR^3l.

Particular A⁹ groups that may be mentioned include halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, and —C(O)NR^3kR^3l. More particular A⁹ groups that may be mentioned include —R^3a, and —N(R^3h)(R³ⁱ).

In a compound of formula I, each B¹ independently represents:

• • (i) halo, NO₂, —CN, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4e)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4h, or —C(O)NR^4kR^4l (“option f(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁴ (“option f(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from D⁵ (“option f(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from D⁶ (“option f(iv)”).

In some embodiments, each B¹ represents a moiety selected from option f(i) and option f(iv). In some particular embodiments, each B¹ represents option f(i). In some other particular embodiments, each B¹ represents option f(iv). In some further embodiments, each B¹ represents a moiety selected from option f(ii), option f(iii) and option f(iv), in particular option f(iii) and option f(iv). In some further embodiments, each B¹ independently represents option f(ii). In still further embodiments, each B¹ independently represents option f(iii).

In some embodiments, in option f(i), each B¹ independently represents a moiety selected from halo, NO₂, —CN, —OR^4b, —N(R^4fN)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, and —C(O)NR^4kR^4l. In some embodiments, in option f(i), each such moiety is selected from halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —(R^4h)(R⁴ⁱ), —C(O)OR^4j, and —C(O)NR^4kR^4l. In some further embodiments, in option f(i), each such moiety is selected from —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ)—C(O)OR^4j, and —C(O)NR^4kR^4l. In some further embodiments, in option f(i), each moiety is selected from —OR^4b, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, and —C(O)NR^4kR^4l. In some further embodiments, in option f(i), each such moiety is selected from —OR^4b, —N(R^4h)(R⁴ⁱ) and —C(O)OR^4j. In some further embodiments, in option f(i), each such moiety is selected from —OR^4b and —N(R^4h)(R⁴ⁱ). In some further embodiments, in option f(i), each such moiety is selected from —OR^4b. In some further embodiments, in option f(i), each such moiety is —N(R^4h)(R⁴ⁱ).

In some embodiments, when B¹ represents —N(R^4h)(R⁴ⁱ), R^4h is H or C_1-6alkyl, e.g. H or C_1-3 alkyl, in particular H or methyl, and R⁴ⁱ is C_1-6 alkyl optionally substituted by one or more groups independently selected from oxy and E¹.

In some embodiments, when R⁴ⁱ represents C_1-6alkyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹, R⁴ⁱ more particularly represents C_1-6 alkyl substituted by one oxy and optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹. In some of these embodiments, R⁴ⁱ represents:

• • (a) —C(O)C_1-6alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, wherein E¹ is as defined herein, or
  • (b) —C(O)E¹, wherein the E¹ attached to the C(O) is as defined herein, e.g. said E¹ represents:
  • aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁴,
  • heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from G⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁶.

In some more particular embodiments, R⁴ⁱ represents:

• • (a) —C(O)C_1-3alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, wherein E¹ is as defined herein, or
  • (b) —C(O)E¹, wherein the E¹ attached to the C(O) is as defined herein, e.g. said E¹ represents:
  • —OR^6b, wherein R^6b is as defined herein,
  • aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁴,
  • heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from G⁵, or heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁶.

In some of the above embodiments, R⁴ⁱ represents —C(O)C_1-3 alkyl, wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, wherein E¹ is as defined herein.

In some of the above embodiments, R⁴ⁱ represents C_1-6 alkoxycarbonyl (e.g. tert-butoxycarbonyl) or C_1-6 alkylcarbonyl (e.g. acetoxy).

In some particular embodiments, R^4h represents H or C_1-6 alkyl (in particular H or C_1-3 alkyl, or H or methyl, e.g. H) and R⁴ⁱ represents H, C_1-6 alkyl, C_1-6 alkoxycarbonyl or C_1-6 alkylcarbonyl.

Some further particular B¹ groups that may be mentioned include —OR^4b and —C(O)OR^4j, such as wherein R^4b represents H and R^4j represents C_1-6 alkyl (e.g. C₁ alkyl).

In some embodiments, in option f(i), B¹ represents a moiety selected from halo (e.g. fluoro), hydroxy, C_1-6 alkoxy (e.g. methoxy or cyclohexyloxy), C_1-6 alkylsulfonsulfonamido (e.g. methylsulfonamido), N—(C_1-6 alkyl)(C_1-6 alkyl)sulfonamido (e.g. N-methylmethylsulfonamido), amino, C_1-6 alkylamino (e.g. methylamino), di-C_1-6 alkylamino (e.g. dimethylamino), carboxy, C_1-6alkoxycarbonyl (e.g. methoxycarbonyl), carbamoyl, C_1-6 alkylcarbamoyl (e.g. methylcarbamoyl), and di-C_1-6 alkylcarbamoyl (e.g. dimethylcarbamoyl), wherein each alkyl is optionally substituted by one or more groups independently selected from oxy and E¹.

In some embodiments, in option f(ii), the phenyl optionally is substituted by 1 or 2 group(s) independently selected from D⁴, e.g. 1 group independently selected from D⁴; e.g. the phenyl is substituted with one group D⁴, which is in para position on the phenyl ring.

In some embodiments, in option f(iii), the heteroaryl is 5- or 6-membered monocyclic heteroaryl. In some embodiments, in option f(iii), the heteroaryl is 5- or 6-membered monocyclic heteroaryl containing from 1 to 3 (e.g. 1 or 2) heteroatoms selected from N, O and S, e.g. from N and O. For example, the heteroaryl may be selected from pyrazolyl, imidazolyl, oxazolyl, pyridinyl, and pyrimidinyl, or from pyrazolyl, imidazolyl, oxazolyl, and pyrimidinyl.

In some embodiments, in option f(iii), the heteroaryl optionally is substituted by 1 or 2 group(s) independently selected from D⁵, e.g. 1 group independently selected from D⁵.

In some embodiments, in option f(iv), the heterocyclyl is selected from 4- to 6-membered heterocyclyl containing one or more heteroatoms selected from N, O and S, e.g. 1 or 3 heteroatoms selected from N, O and S, e.g. from N and O. For example, the heterocyclyl may be selected from piperazinyl, morpholinyl, piperidinyl, pyrrolidinyl, and azetidinyl.

In some embodiments, in option f(iv), the heterocyclyl optionally is substituted by 1 or 2 group(s) independently selected from D⁶, e.g. 1 group independently selected from D⁶.

In a compound of formula I, each B² to B⁴ independently represents

• • (i) halo, NO₂, —CN, —R^4a, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l (“option g(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁴ (“option g(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and D⁵ (“option g(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and D⁶ (“option g(iv)”),

In some embodiments, each B² to B⁴ independently represents option g(i) or option g(iv). In some embodiments, each B² to B⁴ independently represents option g(i).

In some embodiments, in option g(i), B² to B⁴ independently represents a moiety selected from halo, NO₂, —CN, —R^4a, —OR^4b; e.g. halo or —R^4a; in particular —R^4a.

In some embodiments, B² and B³ are absent and B⁴ is as defined herein above.

In a compound of formula I, each R^3a and R^4a represents

• • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹ (“option h(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E² (“option h(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and E³ (“option h(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E⁴ (“option h(iv)”).

In some embodiments, each R^3a and R^4a independently represents option h(i) or option h(iv). In some embodiments, each R^3a and R^4a independently represents option h(i).

In some embodiments, in option h(i) each R^3a and R^4a more particularly represents a moiety selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹; more particularly a moiety selected from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹. In some embodiments, in option h(i), the moiety is selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹; e.g. C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹. In some embodiments, in option h(i) each moiety is selected from methyl and ethyl, in particular methyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹.

In some particular embodiments, each R^3a is as defined herein above and each R^4a is selected from C_1-6alkyl, in particular C_1-3 alkyl, more particularly methyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹. In some particular embodiments, each R^3a is as defined herein above and each R^4a is selected from C_1-6 alkyl, in particular C_1-3 alkyl, more particularly methyl.

In some embodiments, when R^3a is selected from C_1-6alkyl, e.g. C_1-3alkyl, or C₁ alkyl, optionally substituted by one or more E¹, E¹ represents a moiety selected from halo, —OR^6b, —N(R^6h)(R⁶ⁱ), and —C(O)NR^6kR^6l, e.g. from fluoro, OH, NH₂, N(CH₃)₂, and C(O)NH₂.

In some particular embodiments, when any one of A¹-A⁶ (in particular A⁴-A⁶) represents a moiety R^3a, such R^3a is selected from C_1-6 alkyl, e.g. C_1-3 alkyl, or C₁ alkyl, optionally substituted by one or more E¹, e.g. one or more halo, —OR^6b or —N(R^6h)(R⁶ⁱ), in particular one or more halo or —OR^6b, such as one or more fluoro or OH.

In some embodiments, when any one of A⁷-A⁹ represents a moiety R^3a, such R^3a is selected from C_1-6 alkyl, e.g. C_1-3 alkyl, or C₁ alkyl, wherein said alkyl is optionally substituted by one or more E¹, e.g. one or more halo, —OR^6b, —N(R^6h)(R⁶ⁱ), or —C(O)NR^6kR^6l, such as one or more fluoro, OH, NH₂, N(CH₃)₂, or C(O)NH₂.

Thus, in some embodiments, each R^3a:

• • when present in any of A¹-A⁶ (e.g. A⁴-A⁶) independently represents C_1-6 alkyl, e.g. C_1-3 alkyl, or C₁ alkyl, optionally substituted by one or more (e.g. 1-3) E¹, e.g. one or more halo, —OR^6b or —N(R^6h)(R⁶ⁱ), such as one or more moieties selected from fluoro and OH; in particular one or more fluoro; and,
  • when present in any of A⁷-A⁹, independently represents C_1-6alkyl, e.g. C_1-3alkyl, or C₁ alkyl, wherein said alkyl is optionally substituted by one or more (e.g. 1-3) E¹, e.g. one or more moieties selected from halo, —OR^6b, —N(R^6h)(R⁶ⁱ), and —C(O)NR^6kR^6l, such as one or more fluoro, hydroxy, amino, dimethylamino, and carbamoyl.

In a compound of formula I, each R^3b to R^3l, and each R^4b to R^4l independently represents H, or

• • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹ (“option i(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E² (“option i(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and E³ (“option i(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E⁴ (“option i(iv)”).

In some embodiments, each R^3b to R^3l, and each R^4b to R^4l independently represents H, option i(i), or option i(iv). In some further embodiments, each R^3b to R^3l, and each R^4b to R^4l independently represents H, or option i(i).

In some embodiments, in option i(i), each R^3b to R^3l, and each R^4b to R^4l more particularly represents a moiety selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹; e.g. from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹. In some embodiments, such moiety is selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹; e.g. from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹. In some embodiments, R^3b to R^3l and R^4b to R^4l represent methyl or ethyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹.

In some embodiments, any R^3b to R^3l present in a group represented by A¹ to A⁶ (e.g. A⁴ to A⁶) is selected from H and C_1-6alkyl (e.g. H or C_1-3alkyl, or H or C₁ alkyl), wherein the alkyl is optionally substituted by one or more fluoro.

In some embodiments, when any one of A⁷-A⁹ represents a moiety —OR^3b, R^3b in any such A⁷-A⁹ is H or C_1-6 alkyl (e.g. H or C_1-3 alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E¹, e.g. one or more (e.g. 1-3) groups (in particular one group) independently selected from E¹. For example, R^3b in any such A⁷-A⁹ may be selected from H and C_1-6 alkyl (in particular H and C_1-3 alkyl), wherein the alkyl is optionally substituted by —OR^6b or —N(R^6h)(R⁶ⁱ), in particular —N(R^6h)(R⁶ⁱ).

Thus, in some embodiments, each R^3b:

• • when present in any of A¹-A⁶ (e.g. A⁴-A⁶), independently represents H or C_1-6alkyl (e.g. H or C_1-3 alkyl, or H or C₁ alkyl), wherein the alkyl is optionally substituted by one or more fluoro; and,
  • when present in any of A⁷-A⁹, independently represents H or C_1-6alkyl (e.g. H or C_1-3 alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and E, e.g. one or more (e.g. 1-3) groups (in particular one group) independently selected from E¹; e.g. H and C_1-6alkyl (in particular H and C_1-3 alkyl), wherein the alkyl is optionally substituted by —OR^6b or —N(R^6h)(R⁶ⁱ), in particular —N(R^6h)(R⁶ⁱ).

In some embodiments, when any one of A⁷-A⁹ represents a moiety —N(R^3h)(R³ⁱ), R^3h in such A⁷-A⁹ independently represents H or C_1-6 alkyl, and

R^3l in such A⁷-A⁹ independently represents H or

• • (a) C_1-6 alkyl (e.g. C_1-3 alkyl), optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹,
  • (b) —C(O)C_1-6 alkyl (e.g. —C(O)C_1-3 alkyl), optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, wherein E¹ is as defined herein, or
  • (c) —C(O)E¹, wherein E¹ is —OR^6b.

In some of these embodiments, in such A¹-A⁹, R^3h independently represents H or C_1-3 alkyl, e.g. H or methyl, or H.

Thus, in some embodiments, each R^3h and R³ⁱ:

• • when present in any of A¹-A⁶ (e.g. A⁴-A⁶), independently represents H or C_1-6alkyl (e.g. H or C_1-3 alkyl, or H or C₁ alkyl); and,
  • when present in any of A¹-A⁹, R^3h independently represents H or C_1-6 alkyl (e.g. H or C_1-3 alkyl, or H or C₁ alkyl), and R³ⁱ independently represents H or
  • (a) C_1-6 alkyl (e.g. C_1-3 alkyl), optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹,
  • (b) —C(O)C_1-6 alkyl (e.g. —C(O)C_1-3 alkyl), optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, wherein E¹ is as defined herein, or
  • (c) —C(O)E¹, wherein E¹ is —OR^6b.

In some embodiments, when any one of A¹-A⁹ represents a moiety —C(O)NR^3kR^3l, R^3k and R^3l in such A¹-A⁹ independently represents H or C_1-6alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹.

In some further embodiments, when any one of A⁷-A⁹ represents a moiety —C(O)NR^3kR^3l, R^3k in such A¹-A⁹ independently represents H or C_1-6 alkyl, and R^3l in such A⁷-A⁹ independently represents H or C_1-6alkyl (e.g. C_1-3alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, e.g. one or more (e.g. 1-3) groups independently selected from —OR^6b and N(R^6h)(R⁶ⁱ).

In some of these embodiments, in such A¹-A⁹, R^3k independently represents H or C_1-3 alkyl, e.g. H or methyl, or H.

Thus, in some embodiments, each R^3h and R³ⁱ:

• • when present in any of A¹-A⁶, independently represents H or C_1-6alkyl (e.g. H or C_1-3 alkyl, or H or C₁ alkyl); and,
  • when present in any of A¹-A⁹, independently represents H or C_1-6alkyl (e.g. H or C_1-3 alkyl, or H or C₁ alkyl), wherein the alkyl is optionally substituted by one or more (e.g. 1-3) groups independently selected from E¹, e.g. from —OR^6b and —N(R^6h)(R⁶ⁱ).

In some further particular embodiments:

• • R^3a represents C_1-2 alkyl optionally substituted with one or more F;
  • R^3b represents C₁ alkyl optionally substituted with one or more F; and
  • R^3j represents C₁ alkyl.

In a compound of formula I, each D¹ to D⁶ independently represents

• • (i) halo, NO₂, —CN, —R^5a, —OR^5b, —S(O)_qR^5c, —S(O)_rN(Rd)(R^5e), —N(R^5e)S(O)_sR^5g, —N(R^5h)(R⁵ⁱ), —C(O)OR^5j, or —C(O)NR^5kR^5l (“option j(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G¹ (“option j(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and G² (“option j(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and G³ (“option j(iv)”)

In some embodiments, each D¹ to D⁶ independently represents option j(i) or option j(iv). In some further embodiments, each D¹ to D⁶ independently represents option j(i).

In some embodiments, in option j(i), each D¹ to D⁶ independently represents a moiety selected from halo, NO₂, —CN, —R^5a, —OR^5b, or —N(R^5h)(R⁵ⁱ); e.g. —R^5a, —OR^5b, and —N(R^5h)(R⁵ⁱ).

In still further embodiments, D¹ to D³ are absent and each D⁴ to D⁶ is as indicated herein above.

In some embodiments, D⁴ represents —OR^5b.

In some embodiments, D⁵ represents —R^5a or —N(R^5h)(R⁵ⁱ), in particular —R^5a.

In some embodiments, D⁶ represents N(R^5h)(R⁵ⁱ).

In a compound of formula I each E¹ independently represents

• • (i) halo, NO₂, —CN, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e), —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l (“option k(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁴ (“option k(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from G⁵ (“option k(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁶ (“option k(iv)”).

In some embodiments, each E¹ independently represents option k(i) or option k(iv). In some further embodiments, each E¹ independently represents option k(i).

In some embodiments, in option k(i), E¹ more particularly represents a moiety selected from halo, —OR^6b, —N(R^6h)(R⁶ⁱ), and —C(O)NR^6kR^6l. In some embodiments, in option k(i), the moiety more particularly represents —N(R^6h)(R⁶ⁱ) or —C(O)NR^6kR^6l, e.g. —C(O)NR^6kR^6l.

When E¹ is halo, such halo e.g. may be F or Cl, more particularly F.

In some embodiments, each E¹ is selected from halo, hydroxy, C_1-6alkoxy, amino, C_1-6 alkylamino, di-C_1-6 alkylamino, carbamoyl, C_1-6alkylcarbamoyl (e.g. methylcarbamoyl), and di-C_1-6 alkylcarbamoyl (e.g. dimethylcarbamoyl); e.g. from halo, hydroxy, C_1-6 alkoxy, amino, C_1-6 alkylamino, di-C_1-6 alkylamino, and carbamoyl.

In a compound of formula I, each E² to E⁴ independently represents

• • (i) halo, NO₂, —CN, —R^6a, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e), —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l (“option l(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁴ (“option l(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from G⁵ (“option l(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from G⁶ (“option l(iv)”).

In some embodiments, each E² to E⁴ independently represents option l(i) or option l(iv). In some further embodiments, each E² to E⁴ independently represents option l(i).

In some embodiments, in option l(i), each E² to E⁴ more particularly represents a moiety selected from halo, —R^6a, —OR^6b, —N(R^6h)(R⁶ⁱ), - and —C(O)NR^6kR^6l; e.g. from halo and —R^6a. In some embodiments, when any one of E² to E⁴ is halo, such halo e.g. may be F or Cl, more particularly F.

In some embodiments, E² to E⁴ are absent.

In a compound of formula I, each R^5a and R^6a represents

• • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹ (“option m(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J² (“option m(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and J³ (“option m(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J⁴ (“option m(iv)”).

In some embodiments, each R^5a and R^6a independently represents option m(i) or option m(iv). In some embodiments, each R^5a and R^6a represents independently represents option m(i).

In some embodiments, in option m(i), each R^5a and R^6a independently represents a moiety selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹; e.g. each R^5a and R^6a independently represents a moiety selected from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹. In some embodiments, such moiety is selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹; e.g. from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹. In some embodiments, each R^5a and R^6a independently represents methyl or ethyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹. In some embodiments, each R^5a and R^6a independently represents C_1-6 alkyl, e.g. C_1-3alkyl, e.g. methyl.

In some embodiments, R^5a is as defined herein above and R^6a is absent.

In a compound of formula I, each R^5b to R^5l, and R^6b to R^6l independently represents H or

• • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹ (“option n(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J² (“option n(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and J³ (“option n(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J⁴ (“option n(iv)”).

In some embodiments, each R^5b to R^5l, and each R^6b to R^6l independently represents H, option n(i), or option n(iv). In some embodiments, each R^5b to R^5l, and each R^6b to R^6l independently represents H, or option n(i). In some embodiments, each R^5b to R^5l, and each R^6b to R^6l independently represents H.

In some embodiments, in option n(i), each R^5b to R^5l, and each R^6b to R^6l more particularly represents a moiety selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹; e.g. from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and J¹. In some embodiments, such moiety is selected from C_1-6 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹; e.g. from C_1-3 alkyl, optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹. In some embodiments, such moiety is selected from methyl and ethyl, said methyl and ethyl optionally being substituted by one or more (e.g. 1-3) groups independently selected from J¹. In some embodiments, such moiety is methyl optionally substituted by one or more (e.g. 1-3) groups independently selected from J¹. In some embodiments, J¹ is absent. Thus, in some of particular embodiments, each R^5b to R^5l, and R^6b to R^6l represents H or C_1-6 alkyl, e.g. H or C_1-4 alkyl, or H or C_1-3 alkyl, in particular H or methyl, e.g. H.

In a compound of formula I, each G¹ to G⁶ independently represents

• • (i) halo, NO₂, —CN, —R^7a, —OR^7b, —S(O)_qR^7c, —S(O)_rN(R^7d)(R^7e), —N(R^7e)S(O)_sR^7g, —N(R^7h)(R^7l), —C(O)OR^7j, or —C(O)NR^7kR^7l (“option o(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L¹ (“option o(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and L² (“option o(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L³ (“option o(iv)”).

In some embodiments, each G¹ to G⁶ independently represents option o(i) or option o(iv). In some embodiments, each G¹ to G⁶ independently represents option o(i).

In some embodiments, in option o(i), each G¹ to G⁶ independently represents halo, NO₂, —CN, —R^7a, or —OR^7b; in particular halo, or —R^7a. In still further embodiments, G¹ to G⁶ are absent.

In a compound of formula I, each J¹ independently represents

• • (i) halo, NO₂, —CN, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j, or —C(O)NR^8kR^8l (“option p(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from L¹ (“option p(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from L² (“option p(iii)”), or
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from L³ (“option p(iv)”).

In some embodiments, each J¹ independently represents option p(i) or option p(iv). In some embodiments, each J¹ independently represents option p(i).

In some embodiments, in option p(i), each J¹ more particularly may represent halo, NO₂, —CN, —OR^8b, or —N(R^8h)(R⁸ⁱ), in particular halo (e.g. F) or —N(R^8h)(R⁸ⁱ).

In a compound of formula I, each J² to J⁴ independently represents

• • (i) halo, NO₂, —CN, —R^8a, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j, or —C(O)NR^8kR^8l (“option q(i)”),
  • (ii) aryl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L¹ (“option q(ii)”),
  • (iii) heteroaryl optionally substituted by one or more (e.g. 1-3) groups selected from oxy and L² (“option q(iii)”),
  • (iv) heterocyclyl optionally substituted by one or more (e.g. 1-3) groups independently selected from oxy and L³ (“option q(iv)”).

In some embodiments, each J¹ independently represents option q(i) or option q(iv). In some embodiments, each J¹ independently represents option q(i).

In some embodiments, in option q(i), each J² to J⁴ more particularly may represent halo, NO₂, —CN, —R^8a, —OR^1b, or —N(R^8h)(R⁸ⁱ), in particular halo (e.g. F), —R^8a, or —N(R^8h)(R⁸ⁱ), or halo or —R^8a. In still further embodiments, J² to J⁴ are absent.

In a compound of formula I, each L¹ to L³ independently represents halo, NO₂, —CN, —R^9a, —OR^9b, —S(O)_qR^9c, —S(O)_rN(R^9d) (R^9e), —N(R^9f)S(O)_sR^9g, —N(R^9h)(R⁹ⁱ), —C(O)OR^9j, or —C(O)NR^9kR^9l. In some embodiments, each L¹ to L³ independently represents halo, NO₂, —CN, —Ra, or —OR, e.g. halo or —R^9a. In some embodiments, L¹ to L³ are absent.

In a compound of formula I, each R^7a, R^8a and R^9a represents C_1-3 alkyl optionally substituted with one or more fluoro; and each R^7b to R^7l, R^8b to R^8l and R^9b to R^9l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro. In some embodiments, each R^7a, R^8a and R^9a represents methyl optionally substituted with one or more fluoro; and each R^7b to R^7l, R^8b to R^8l and R^9b to R^9l independently represents H or methyl optionally substituted with one or more fluoro.

In a compound of formula I each q, r and s independently represents 0, 1 or 2. In some embodiments, each q, r and s independently represents 0 or 2. In some embodiments, each q, r and s represents 2. In some embodiments, q represents 0 or 2, and r and s represent 2.

In some particular embodiments of a compound of formula I:

• • R² represents any one of options a(i) to a(iii);
  • each R³ independently represents any one of options b(i) to b(iv);
  • each R^2a independently represents any one of options c(i) and c(iv);
  • each R^2b to R^2l independently represents H or any one of options d(i) and d(iv);
  • each A⁴ to A⁹ independently represents option e(i);
  • each B¹ independently represents any one of options f(i) to f(iv);
  • each B⁴ independently represents option g(i);
  • each R^3a and R^4a independently represents option h(i);
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or option i(i);
  • each D⁴ to D⁶ independently represents option j(i);
  • each E¹ independently represents options k(i) or k(iv);
  • each R^5a and R^6a independently represents option l(i);
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or option m(i);
  • each J¹ independently represents any one of options n(i) and n(iv);
  • each R^8a represents C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^8b to R^8l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each L³ independently represents halo, NO₂, —CN, —R^9a, —OR^9b, —S(O)_qR^9c, —S(O)_rN(R^9d)(R^9e), —N(R^9f)S(O)_sR^9g, —N(R^9h)(R⁹ⁱ), —C(O)OR^9j, or —C(O)NR^9kR^9l;
  • each R^9a independently represents C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^9b to R^9l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro; and
  • each q, r and s independently represents 0, 1 or 2.

In some of these particular embodiments:

• • R² represents any one of options a(i) to a(iii);
  • each R³ independently represents any one of options b(i) to b(iv);
  • each R^2a independently represents option c(i);
  • each R^2b to R^2l independently represents H or option d(i);
  • each A⁴ to A⁹ independently represents option e(i);
  • each B¹ independently represents any one of options f(i) to f(iv);
  • each B⁴ independently represents option g(i);
  • each R^3a and R^4a independently represents option h(i);
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or option i(i);
  • each D⁴ to D⁶ independently represents option j(i);
  • each E¹ independently represents option k(i);
  • each R^5a and R^6a independently represents option l(i);
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or option m(i); and
  • each J¹ independently represents option n(i).

In some further of these particular embodiments:

• • R² represents option a(i);
  • R³ represents option b(i);
  • each R^2a independently represents option c(i);
  • each R^2b to R^2l independently represents H or option d(i);A⁴ represents option e(i);
  • each B¹ independently represents any one of options f(i) to f(iv);
  • each R^3a and R^4a independently represents option h(i);
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or option i(i);
  • each D⁴ to D⁶ independently represents option j(i);
  • each E¹ independently represents option k(i);
  • each R^5a and R^6a independently represents option l(i);
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or option m(i); and
  • each J¹ independently represents option n(i).

In some further of these particular embodiments:

• • R² represents option a(i);
  • R³ represents option b(i);
  • each R^2a independently represents option c(i);
  • each R^2b to R^2l independently represents H or option d(i);
  • A⁴ represents option e(i);
  • each B¹ independently represents any one of options f(i) and f(iv); in particular option f(i);
  • each R^3a and R^4a independently represents option h(i);
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or option i(i);
  • each D⁴ to D⁶ independently represents option j(i);
  • each E¹ independently represents option k(i);
  • each R^5a and R^6a independently represents option l(i);
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or option m(i); and
  • each J¹ independently represents option n(i).

For the avoidance of doubt, it is pointed out that, for example, the indication that “R³ represents option b(i)” should be understood to mean that “R³ represents (i) halo, —NO₂, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —S(O)_rN(R^2d) (R^2e), —N(R^2f)S(O)_sR^2g, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l”, and thus such two expressions may replace each other.

As a further illustrating example, the indication that “each B¹ independently represents any one of options f(i) and f(iv)” should be understood to mean that “each B¹ independently represents

• • (i) halo, NO₂, —CN, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l, or
  • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶”,and thus such two expressions may replace each other.

In some particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —NO₂, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —S(O)_rN(R^2d)(R^2e), —N(R^2f)S(O)_sR^2g, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
    • (ii) aryl optionally substituted by one or more groups independently selected from A⁷
    • (iii) heteroaryl optionally substituted by one or more groups selected from A⁸, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from A;
  • each R^2a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^1b to R^1l and R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
    • (ii) aryl optionally substituted by one or more groups independently selected from oxy and B²,
    • (iii) heteroaryl optionally substituted by one or more groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from oxy and B⁴;
  • each A⁴ to A⁹ independently represents
    • (ii) halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, NO₂, —CN, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each B² to B⁴ independently represents
    • (ii) halo, NO₂, —CN, —R^4a, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l;
  • each R^3a and R^4a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E¹;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E¹;
  • each D⁴ to D⁶ independently represents
    • (i) halo, NO₂, —CN, —R^5a, —OR^5b, —S(O)_qR^5c, —S(O)_rN(R^5d)(R^5e), —N(R^5f)S(O)_sR^5g, —N(R^5h)(R⁵ⁱ), —C(O)OR^5j, or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, NO₂, —CN, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e). —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, NO₂, —CN, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j—, or —C(O)NR^8kR^8l,
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from L³;
  • each R^8b to R^3l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each L³ independently represents halo, NO₂, —CN, —R^9a, —OR^9b, —S(O)_qR^9c, —S(O)_rN(R^9d)(R^9e), —N(R^9f)S(O)_sR^9g, —N(R^9h)(R⁹ⁱ), —C(O)OR^9j, or —C(O)NR^9kR^9l,
  • each R^9a independently represents C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^9b to R^9l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro; and
  • each q, r and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —NO₂, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —S(O)_rN(R^2d)(R^2e), —N(R^2f)S(O)_sR^2g, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
    • (ii) aryl optionally substituted by one or more groups independently selected from A⁷,
    • (iii) heteroaryl optionally substituted by one or more groups selected from A⁸, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from A⁹;
  • each R^2a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
    • (iii) heteroaryl optionally substituted by one or more groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from oxy and B⁴;
  • each A⁴ to A⁹ independently represents
    • (i) halo, NO₂, —CN, —R^3a, —OR^3b, —S(O)_qR^3c, —S(O)_rN(R^3d)(R^3e), —N(R^3f)S(O)_sR^3g, —N(R^3h)(R³ⁱ), —C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, NO₂, —CN, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each B³ to B⁴ independently represents
    • (i) halo, NO₂, —CN, —R^4a, —OR^4b, —S(O)_qR^4c, —S(O)_rN(R^4d)(R^4e), —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l;
  • each R^3a and R^4a represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E¹;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E;
  • each D⁴ to D⁶ independently represents
    • (i) halo, NO₂, —CN, —R^5a, —OR^5b, —S(O)_qR^5c, —S(O)_rN(R^5d)(R^5e), —N(R^5e)S(O)_sR^5g, —N(R^5h)(R⁵ⁱ), —C(O)OR^5j, or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, NO₂, —CN, —OR^6b, —S(O)_qR^6c, —S(O)_rN(R^6d)(R^6e), —N(R^6f)S(O)_sR^6g, —N(R^6h)(R⁶ⁱ), —C(O)OR^6j, or —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R⁵¹, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, NO₂, —CN, —OR^8b, —S(O)_qR^8c, —S(O)_rN(R^8d)(R^8e), —N(R^8f)S(O)_sR^8g, —N(R^8h)(R⁸ⁱ), —C(O)OR^8j, or —C(O)NR^8kR^8l,
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from L³;
  • each R^8b to R^8l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each L³ independently represents halo, NO₂, —CN, —R^9a, —OR^9b, —S(O)_qR^9c, —S(O)_rN(R^9d)(R^9e), —N(R^9f)S(O)_sR^9g, —N(R^9h)(R⁹ⁱ), —C(O)OR^9j, or —C(O)NR^9kR^9l,
  • each R^9a independently represents C_1-3 alkyl optionally substituted with one or more fluoro;
  • each R^9b to R^9l independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro; and
  • each q, r and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR²ⁱ, or —C(O)NR^2kR^2l,
    • (ii) aryl optionally substituted by one or more groups independently selected from A⁷
    • (iii) heteroaryl optionally substituted by one or more groups selected from A⁸, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from A⁹;
  • each R^2a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
    • (iii) heteroaryl optionally substituted by one or more groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from oxy and B⁴;
  • each A⁴ to A⁹ independently represents
    • (i) halo, —CN, —R^3a, —OR^3b, —S(O)_rN(R^3d)(R^3e), —N(R^3h)(R³ⁱ)—C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each B³ and B⁴ independently represents —R^4a;
  • each R^3a and R^4a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E;
  • each D⁴ to D⁶ independently represents
    • (i) —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l, each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R^6l), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, or —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl,
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q, r and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
    • (ii) aryl optionally substituted by one or more groups independently selected from A⁷,
    • (iii) heteroaryl optionally substituted by one or more groups selected from A⁸, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from A⁹;
  • each R^2a independently represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, optionally substituted by one or more groups independently selected from oxy and B¹;
    • (iii) heteroaryl optionally substituted by one or more groups selected from oxy and B³, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from oxy and B⁴;
  • each A⁴ to A⁹ independently represents
    • (ii) halo, —CN, —R^3a, —OR^3b, —S(O)_rN(R^3d)(R^3e), —N(R^3h)(R³ⁱ)—C(O)OR^3j, or C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each B³ and B⁴ independently represents —R^4a;
  • each R^3a and R^4a independently represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E;
  • each D⁴ to D⁶ independently represents
    • (i) —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R⁶ⁱ), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, or —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl,
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q, r and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
  • each R^2a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each A⁴ to A⁶ independently represents
    • (i) halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ), —C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each R^3a and R^4a represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E¹;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E¹;
  • each D⁴ to D⁶ independently represents
    • (i) halo, —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R⁶ⁱ), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl;
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)R^2j, or —C(O)NR^2kR^2l,
  • each R^2a independently represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each A⁴ independently represents
    • (i) halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)—C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each R^3a and R^4a represent
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and E;
  • each D⁴ to D⁶ independently represents
    • (i) halo, —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R⁶ⁱ), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl;
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
    • (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁵, or
    • (iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one or more groups selected from oxy and A⁶;
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
  • each R^2a independently represents
    • (i) C_1-6 alkyl, wherein each such alkyl is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each A⁴ to A⁶ independently represents
    • (i) halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)—C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each R^3a and R^4a independently represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E¹;
  • each D⁴ to D⁶ independently represents
    • (i) halo, —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R⁶ⁱ), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl;
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q and s independently represents 0, 1 or 2.

In some further particular embodiments of a compound of formula I:

• • each R¹ independently represents fluoro, methyl or hydroxy;
  • n represents 0, 1 or 2; preferably 0 or 1, more preferably 0;
  • R² represents
    • (i) phenyl optionally substituted by one or more groups independently selected from A⁴,
  • each R³ independently represents
    • (i) halo, —CN, —R^2a, —OR^2b, —S(O)_qR^2c, —N(R^2h)(R²ⁱ), —C(O)OR^2j, or —C(O)NR^2kR^2l,
  • each R^2a independently represents
    • (i) C_1-6 alkyl, wherein each such alkyl is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each R^2b to R^2l independently represents H or
    • (i) C_1-6 alkyl, C_2-6 alkenyl or C_2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B¹;
  • each A⁴ independently represents
    • (i) halo, —CN, —R^3a, —OR^3b, —N(R^3h)(R³ⁱ)C(O)OR^3j, or —C(O)NR^3kR^3l,
  • each B¹ independently represents
    • (i) halo, —OR^4b, —N(R^4f)S(O)_sR^4g, —N(R^4h)(R⁴ⁱ), —C(O)OR^4j, or —C(O)NR^4kR^4l,
    • (ii) aryl optionally substituted by one or more groups independently selected from D⁴,
    • (iii) heteroaryl optionally substituted by one or more groups selected from D⁵, or
    • (iv) heterocyclyl optionally substituted by one or more groups independently selected from D⁶;
  • each R^3a and R^4a independently represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E;
  • each R^3b to R^3l, and R^4b to R^4l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and E;
  • each D⁴ to D⁶ independently represents
    • (i) halo, —R^5a, —OR^5b, —N(R^5h)(R⁵ⁱ), or —C(O)NR^5kR^5l,
  • each E¹ independently represents
    • (i) halo, —OR^6b, —N(R^6h)(R⁶ⁱ), —C(O)NR^6kR^6l, or
    • (iv) heterocyclyl;
  • each R^5a represents
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each R^5b to R^5l, and R^6b to R^6l independently represents H or
    • (i) C_1-6 alkyl, optionally substituted by one or more groups independently selected from oxy and J¹;
  • each J¹ independently represents
    • (i) halo, —N(R^8h)(R⁸ⁱ), or
    • (iv) heterocyclyl;
  • each R^8h and R⁸ⁱ independently represents H or C_1-3 alkyl optionally substituted with one or more fluoro;
  • each q and s independently represents 0, 1 or 2.

In the above mentioned embodiments, any aryl preferably is phenyl; any heteroaryl preferably is monocyclic, 5- or 6-membered and contains 1, 2 or 3 heteroatoms selected from N, O and S; any heterocyclyl preferably is 4- to 6-membered and contains 1, 2 or 3 heteroatoms selected from N, O and S.

In the above mentioned embodiments, when R² is an optionally substituted phenyl, such phenyl more preferably is substituted by at least one group A⁴.

It should be realized that, unless otherwise indicated or apparent from the context, any reference made herein to a compound of formula I also should be construed as a reference to a compound of any one of the formulas Ia-In.

Particular compounds of the invention that may be mentioned include those compounds as described in the examples provided herein, and pharmaceutically acceptable salts thereof. For the avoidance of doubt, where such compounds of the invention include compounds in a particular salt form, compounds of the invention include those compounds in non-salt form and in the form of any pharmaceutically acceptable salt thereof (which may include the salt form present in such examples).

In some embodiments, the compound of formula I is not 4-(2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-phenylpiperidine-1-carboxamide, or 4-(5-methylsulfonyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide.

Medical Uses

As indicated herein, the compounds of the invention, and therefore compositions and kits comprising the same, are useful as pharmaceuticals.

Thus, according to a second aspect of the invention there is provided a compound of the invention, as hereinbefore defined (i.e. a compound as defined in the first aspect of the invention, including all embodiments and particular features thereof), for use as a pharmaceutical (or for use in medicine).

For the avoidance of doubt, references to compounds as defined in the first aspect of the invention will include references to compounds of formula I (including all embodiments thereof, such as compounds of formula Ia, Ib and Ic) and pharmaceutically acceptable salts thereof.

Although compounds of the invention may possess pharmacological activity as such, certain pharmaceutically acceptable (e.g. “protected”) derivatives of compounds of the invention may exist or be prepared which may not possess such activity, but may be administered parenterally or orally and thereafter be metabolized in the body to form compounds of the invention. Such compounds (which may possess some pharmacological activity, provided that such activity is appreciably lower than that of the active compounds to which they are metabolized) may therefore be described as “prodrugs” of compounds of the invention.

As used herein, references to prodrugs will include compounds that form a compound of the invention, in an experimentally-detectable amount, within a predetermined time, following enteral or parenteral administration (e.g. oral or parenteral administration). All prodrugs of the compounds of the invention are included within the scope of the invention.

Furthermore, certain compounds of the invention may possess no or minimal pharmacological activity as such, but may be administered parenterally or orally, and thereafter be metabolized in the body to form compounds of the invention that possess pharmacological activity as such. Such compounds (which also includes compounds that may possess some pharmacological activity, but that activity is appreciably lower than that of the active compounds of the invention to which they are metabolized), may also be described as “prodrugs”.

For the avoidance of doubt, compounds of the invention are therefore useful because they possess pharmacological activity, and/or are metabolized in the body following oral or parenteral administration to form compounds that possess pharmacological activity.

As described herein, compounds of the invention may be particularly useful in treating cell proliferation disorders, which the skilled person will understand as being diseases and disorders characterized by abnormal cell proliferation.

Thus, in a third aspect of the invention, there is provided a compound of the invention, as hereinbefore defined, for use in the treatment of a cell proliferation disorder.

In an alternative third aspect of the invention, there is provided a method of treating a cell proliferation disorder comprising administering to a patient in need thereof a therapeutically effective amount of a compound of the invention, as hereinbefore defined.

In a further alternative third aspect of the invention, there is provided the use of a compound of the invention, as hereinbefore defined, for the manufacture of a medicament for the treatment a cell proliferation disorder.

The skilled person will understand that references to the treatment of a particular condition (or, similarly, to treating that condition) will take their normal meanings in the field of medicine. In particular, the terms may refer to achieving a reduction in the severity and/or frequency of occurrence of one or more clinical symptom associated with the condition, as adjudged by a physician attending a patient having or being susceptible to such symptoms.

As used herein, references to a patient (or to patients) will refer to a living subject being treated, including mammalian (e.g. human) patients. In particular, references to a patient will refer to human patients.

For the avoidance of doubt, the skilled person will understand that such treatment will be performed in a patient (or subject) in need thereof. The need of a patient (or subject) for such treatment may be assessed by those skilled the art using routine techniques.

As used herein, the terms disease and disorder (and, similarly, the terms condition, illness, medical problem, and the like) may be used interchangeably.

As used herein, the term effective amount will refer to an amount of a compound that confers a therapeutic effect on the treated patient. The effect may be observed in a manner that is objective (i.e. measurable by some test or marker) or subjective (i.e. the subject gives an indication of and/or feels an effect). In particular, the effect may be observed (e.g. measured) in a manner that is objective, using appropriate tests as known to those skilled in the art.

The skilled person will be able to identify various diseases and disorders characterized by abnormal cell proliferation.

In particular embodiments (i.e. particular embodiments of the third aspect of the invention), the cell proliferation disorder is a selected from the group consisting of: (a) cancer; and (b) inflammation.

As described herein, the compounds of the first aspect of the invention may find particular utility in the treatment of inflammation. Thus, in certain embodiments, the cell proliferation disorder is inflammation.

In particular embodiments, the inflammation is an acute and/or systemic inflammation.

In more particular embodiments, the inflammation is an inflammation of the:

• • lungs (such as asthma, chronic obstructive pulmonary disease (COPD), acute lung injury/acute respiratory distress and/or interstitial lung disease);
  • joints (such as rheumatoid arthritis);
  • digestive system, e.g. the intestine (such as ulcerative colitis and/or Chron's disease); skin (such as eczema and/or psoriasis); and/or
  • liver (such as inflammation resulting from chronic hepatitis).

Particular types of inflammation that may be mentioned include inflammation of the lungs (such as asthma, chronic obstructive pulmonary disease (COPD), acute lung injury/acute respiratory distress and/or interstitial lung disease).

In further embodiments, the inflammation may also be systemic inflammation triggered by an autoimmune response, as may occur in conditions such as sepsis.

As also described herein, the compounds of the first aspect of the invention may find particular utility in the treatment of cancers. Thus, in certain embodiments, the cell proliferation disorder is cancer (i.e. a cancer). In particular embodiments, the cancer is a solid tumour cancer. In further embodiments, the cancer is a blood cell cancer, such as leukaemia. In more particular embodiments, the cancer is selected from the group consisting of:

• • leukemia (such as acute lymphoblastic leukemia, acute monocytic leukemia, acute myelogenous leukemia, chronic myelogenous leukemia, acute myeloid leukemia, acute Promyelocytic leukemia, and/or acute promyelocytic leukemia);
  • lymphomas (such as Burkitt's lymphoma);
  • carcinomas, including adenocarcinomas (such as lung carcinoma, e.g. large cell lung carcinoma and/or small cell lung carcinoma, cervical adenocarcinoma, colorectal adenocarcinoma, colorectal carcinoma, prostate carcinoma, e.g. prostate adenocarcinoma, renal carcinoma, e.g. renal cell adenocarcinoma and/or endometrioid adenocarcinoma);
  • lymphoblastoma;
  • glioblastomas (such as glioblastoma multiforme and/or malignant glioblastoma);
  • lymphomas (such as mantle cell lymphoma); and/or
  • sarcomas (such as osteosarcoma).

Specific cancers that may be mentioned include lung cancer (e.g. large cell lung cancer and small cell lung cancer), breast cancer, renal cancer, colorectal cancer, prostate cancer, brain cancer (e.g. glioblastoma) and leukaemia. More particular cancers that may be mentioned include lung cancer (e.g. large cell lung cancer and small cell lung cancer). Further cancers that may be mentioned include those cancers expressing a relevant oncogene (i.e. an oncogene specific to that cancer types), as known to those skilled in the art (such as Ras).

Pharmaceutical Compositions

As described herein, compounds of the invention are useful as pharmaceuticals. Such compounds may be administered alone or may be administered by way of known pharmaceutical compositions/formulations.

In a fourth aspect of the invention, there is provided a pharmaceutical composition comprising a compound of the invention as defined herein, and optionally one or more pharmaceutically acceptable excipient.

As used herein, the term pharmaceutically acceptable excipients includes references to vehicles, adjuvants, carriers, diluents, pH adjusting and buffering agents, tonicity adjusting agents, stabilizers, wetting agents and the like. In particular, such excipients may include adjuvants, diluents or carriers.

For the avoidance of doubt, references herein to compounds of invention being for particular uses (and, similarly, to uses and methods of use relating to compounds of the invention) may also apply to pharmaceutical compositions comprising compounds of the invention, as described herein.

Thus, in a fifth aspect of the invention, there is provided a pharmaceutical composition as defined in the fourth aspect of the invention for use in the treatment a cell proliferation disorder (as defined herein, with reference to the third aspect of the invention and all embodiments thereof).

The skilled person will understand that compounds of the invention may act systemically and/or locally (i.e. at a particular site), and may therefore be administered accordingly using suitable techniques known to those skilled in the art.

The skilled person will understand that compounds and compositions as described herein will normally be administered orally, intravenously, subcutaneously, buccally, rectally, dermally, nasally, tracheally, bronchially, sublingually, intranasally, topically, by any other parenteral route or via inhalation, in a pharmaceutically acceptable dosage form.

Pharmaceutical compositions as described herein will include compositions in the form of tablets, capsules or elixirs for oral administration, suppositories for rectal administration, sterile solutions or suspensions for parenteral or intramuscular administration, and the like. Alternatively, particularly where such compounds of the invention act locally, pharmaceutical compositions may be formulated for topical administration.

Thus, in particular embodiments, the pharmaceutical formulation is provided in a pharmaceutically acceptable dosage form, including tablets or capsules, liquid forms to be taken orally or by injection, suppositories, creams, gels, foams, inhalants (e.g. to be applied intranasally), or forms suitable for topical administration. For the avoidance of doubt, in such embodiments, compounds of the invention may be present as a solid (e.g. a solid dispersion), liquid (e.g. in solution) or in other forms, such as in the form of micelles.

For example, in the preparation of pharmaceutical formulations for oral administration, the compound may be mixed with solid, powdered ingredients such as lactose, saccharose, sorbitol, mannitol, starch, amylopectin, cellulose derivatives, gelatin, or another suitable ingredient, as well as with disintegrating agents and lubricating agents such as magnesium stearate, calcium stearate, sodium stearyl fumarate and polyethylene glycol waxes. The mixture may then be processed into granules or compressed into tablets.

Soft gelatin capsules may be prepared with capsules containing one or more active compounds (e.g. compounds of the first and, therefore, second and third aspects of the invention, and optionally additional therapeutic agents), together with, for example, vegetable oil, fat, or other suitable vehicle for soft gelatin capsules. Similarly, hard gelatine capsules may contain such compound(s) in combination with solid powdered ingredients such as lactose, saccharose, sorbitol, mannitol, potato starch, corn starch, amylopectin, cellulose derivatives or gelatin.

Dosage units for rectal administration may be prepared (i) in the form of suppositories which contain the compound(s) mixed with a neutral fat base; (ii) in the form of a gelatin rectal capsule which contains the active substance in a mixture with a vegetable oil, paraffin oil, or other suitable vehicle for gelatin rectal capsules; (iii) in the form of a ready-made micro enema; or (iv) in the form of a dry micro enema formulation to be reconstituted in a suitable solvent just prior to administration.

Liquid preparations for oral administration may be prepared in the form of syrups or suspensions, e.g. solutions or suspensions, containing the compound(s) and the remainder of the formulation consisting of sugar or sugar alcohols, and a mixture of ethanol, water, glycerol, propylene glycol and polyethylene glycol. If desired, such liquid preparations may contain colouring agents, flavouring agents, saccharine and carboxymethyl cellulose or other thickening agent. Liquid preparations for oral administration may also be prepared in the form of a dry powder to be reconstituted with a suitable solvent prior to use.

Solutions for parenteral administration may be prepared as a solution of the compound(s) in a pharmaceutically acceptable solvent. These solutions may also contain stabilizing ingredients and/or buffering ingredients and are dispensed into unit doses in the form of ampoules or vials. Solutions for parenteral administration may also be prepared as a dry preparation to be reconstituted with a suitable solvent extemporaneously before use.

Depending on e.g. potency and physical characteristics of the compound of the invention (i.e. active ingredient), pharmaceutical formulations that may be mentioned include those in which the active ingredient is present in an amount that is at least 1% (or at least 10%, at least 30% or at least 50%) by weight. That is, the ratio of active ingredient to the other components (i.e. the addition of adjuvant, diluent and carrier) of the pharmaceutical composition is at least 1:99 (or at least 10:90, at least 30:70 or at least 50:50) by weight.

The skilled person will understand that compounds of the invention may be administered (for example, as formulations as described hereinabove) at varying doses, with suitable doses being readily determined by one of skill in the art. Oral, pulmonary and topical dosages (and subcutaneous dosages, although these dosages may be relatively lower) may range from between about 1 mg/kg of body weight per day (mg/kg/day) to about 200 mg/kg/day. For example, treatment with such compounds may comprise administration of a formulations typically containing between about 100 mg to about 10,000 mg, such as a dose of about 6,000 mg, of the active ingredient(s). Advantageously, treatment may comprise administration of such compounds and compositions in a single daily dose, or the total daily dosage may be administered in divided doses of two, three or four times daily.

When used herein in relation to a specific value (such as an amount), the term “about” (or similar terms, such as “approximately”) will be understood as indicating that such values may vary by up to 10% (particularly, up to 5%, such as up to 1%) of the value defined. It is contemplated that, at each instance, such terms may be replaced with the notation “±10%”, or the like (or by indicating a variance of a specific amount calculated based on the relevant value). It is also contemplated that, at each instance, such terms may be deleted.

For the avoidance of doubt, the skilled person (e.g. the physician) will be able to determine the actual dosage which will be most suitable for an individual patient, which is likely to vary with the route of administration, the type and severity of the condition that is to be treated, as well as the species, age, weight, sex, renal function, hepatic function and response of the particular patient to be treated. Although the above-mentioned dosages are exemplary of the average case, there can, of course, be individual instances where higher or lower dosage ranges are merited, and such doses are within the scope of the invention.

Combinations and Kits-of-Parts

The skilled person will understand that treatment with compounds of the invention may further comprise (i.e. be combined with) further treatment(s) for the same condition. In particular, treatment with compounds of the invention may be combined with means for the treatment of a cell proliferation disorder as described herein (such as inflammation and/or cancer, as described herein), such as treatment with one or more other therapeutic agent that is useful in the in the treatment of a cell proliferation disorder and/or one or more physical method used in the treatment of a cell proliferation disorder (such as, particularly in the treatment of cancer, treatment through surgery), as known to those skilled in the art.

As described herein, compounds of the invention may also be combined with one or more other (i.e. different) therapeutic agents (i.e. agents that are not compounds of the invention) that are useful in the treatment of a cell proliferation disorder. Such combination products that provide for the administration of a compound of the invention in conjunction with one or more other therapeutic agent may be presented either as separate formulations, wherein at least one of those formulations comprises a compound of the invention, and at least one comprises the other therapeutic agent, or may be presented (i.e. formulated) as a combined preparation (i.e. presented as a single formulation including a compound of the invention and the one or more other therapeutic agent).

Thus, according to a sixth aspect of the invention, there is provided a combination product comprising:

• • (I) a compound of the invention, as hereinbefore defined (i.e. in the first aspect of the invention, including all embodiments and particular features thereof); and
  • (II) one or more other therapeutic agent that is useful in the treatment of a cell proliferation disorder (such as inflammation and/or cancer, as described herein),
  • wherein each of components (1) and (II) is formulated in admixture, optionally with one or more a pharmaceutically acceptable excipient.

In a seventh aspect of the invention, there is provided a kit-of-parts comprising:

• • (a) a pharmaceutical formulation as hereinbefore defined (i.e. in the fifth aspect of the invention); and
  • (b) one or more other therapeutic agent that is useful in the treatment of a cell proliferation disorder (such as cancer or inflammation, as described herein), optionally in admixture with one or more pharmaceutically acceptable excipient,
  • which components (a) and (b) are each provided in a form that is suitable for administration in conjunction (i.e. concomitantly or sequentially) with the other.

With respect to the kits-of-parts as described herein, by “administration in conjunction with” (and similarly “administered in conjunction with”) we include that respective formulations are administered, sequentially, separately or simultaneously, as part of a medical intervention directed towards treatment of the relevant condition. Thus, in relation to the present invention, the term “administration in conjunction with” (and similarly “administered in conjunction with”) includes that the two active ingredients (i.e. a compound of the invention and a further agent for the treatment of a cell proliferation disorder, or compositions comprising the same) are administered (optionally repeatedly) either together, or sufficiently closely in time, to enable a beneficial effect for the patient, that is greater, over the course of the treatment of the relevant condition, than if either agent is administered (optionally repeatedly) alone, in the absence of the other component, over the same course of treatment. Determination of whether a combination provides a greater beneficial effect in respect of, and over the course of, treatment of a particular condition will depend upon the condition to be treated but may be achieved routinely by the skilled person.

Further, in the context of the present invention, the term “in conjunction with” includes that one or other of the two formulations may be administered (optionally repeatedly) prior to, after, and/or at the same time as, administration of the other component. When used in this context, the terms “administered simultaneously” and “administered at the same time as” includes instances where the individual doses of the compound of the invention and the additional compound for the treatment of cancer, or pharmaceutically acceptable salts thereof, are administered within 48 hours (e.g. within 24 hours, 12 hours, 6 hours, 3 hours, 2 hours, 1 hour, 45 minutes, 30 minutes, 20 minutes or 10 minutes) of each other.

Other therapeutic agents useful in the treatment of a cell proliferation disorder (such as those known for use in the treatment of cancer or inflammation as described herein) will be well-known to those skilled in the art. For example, therapeutic agents that may be mentioned (particularly, when for use in the treatment of cancer) include MTH1 inhibitors (such as karonudib, and MTH1 inhibitors as described in WO 2014/084778 A1, WO 2015/187088 A1 and WO 2015/187089 A1) and tubulin inhibitors (i.e. poisons) (such as paclitaxel).

Other examples of therapeutic agents that may be mentioned are anti-microtubule agents, platinum coordination complexes, alkylating agents, antibiotic agents, topoisomerase II inhibitors, antimetabolites, topoisomerase I inhibitors, hormones and hormonal analogues, signal transduction pathway inhibitors; kinase inhibitors; angiogenesis inhibitors; immunotherapeutic agents; pro-apoptotic agents; and cell cycle signaling inhibitors.

Preparation of Compounds/Compositions

Pharmaceutical compositions/formulations, combination products and kits as described herein may be prepared in accordance with standard and/or accepted pharmaceutical practice. Thus, in a further aspect of the invention there is provided a process for the preparation of a pharmaceutical composition/formulation, as hereinbefore defined, which process comprises bringing into association a compound of the invention, as hereinbefore defined, with one or more pharmaceutically acceptable excipient.

In further aspects of the invention, there is provided a process for the preparation of a combination product or kit-of-parts as hereinbefore defined, which process comprises bringing into association a compound of the invention, as hereinbefore defined, with the other therapeutic agent that is useful in the treatment of the relevant disease or disorder, and at least one pharmaceutically acceptable excipient.

As used herein, references to bringing into association will mean that the two components are rendered suitable for administration in conjunction with each other.

Thus, in relation to the process for the preparation of a kit-of-parts as hereinbefore defined, by bringing the two components “into association with” each other, we include that the two components of the kit-of-parts may be:

• • (i) provided as separate formulations (i.e. independently of one another), which are subsequently brought together for use in conjunction with each other in combination therapy; or
  • (ii) packaged and presented together as separate components of a “combination pack” for use in conjunction with each other in combination therapy.

Compounds of the invention as described herein may be prepared in accordance with techniques that are well known to those skilled in the art, such as those described in the examples provided hereinafter.

According to an eighth aspect of the invention a process is provided, for the preparation of a compound of the invention as hereinbefore defined, comprising:

• • (i) for compounds of formula I wherein X¹ represents O, reacting a compound of formula II

• • wherein R¹, R², X², Y¹ to Y⁴, Z to Z³, and n are as defined herein (i.e. in the first aspect of the invention, including all embodiments thereof), with phosgene or a suitable equivalent thereof (e.g. a source of phosgene, such as diphosgene or triphosgene, or a functional equivalent. such as carbonyl diimidazole), in the presence of a suitable solvent (such as DCM) and a suitable base (such as an amine base, e.g. N,N-diisopropylethylamine);
  • (ii) for compounds of formula I wherein Z³ represents N, reaction of a compound of formula III

• • wherein R¹, X¹, Y¹ to Y⁴, Z¹, Z², and n are as defined herein, with a compound of formula IV

• • or a suitable salt thereof (e.g. a trifluoroacetate salt), wherein X² and R² are as defined herein, in the presence of a suitable solvent (such as DCM) and a suitable base (such as an amine base, e.g. N,N-diisopropylethylamine);
  • (iii) reaction of a compound of formula III as defined herein with a compound of formula V

• • wherein R² is as defined herein, and with phosgene or a suitable equivalent thereof (such as diphosgene or triphosgene), in the presence of a suitable solvent (such as DCM) and a suitable base (such as an amine base, e.g. N,N-diisopropylethylamine);
  • (iv) where Z³ represents CH or CR¹ (e.g. CH), reaction of a compound of formula VI

• • wherein R¹, X¹, Y¹ to Y⁴, Z¹, Z², and n are as defined herein, with a compound of formula V as defined herein, in presence of a suitable coupling agent (such as propylphosphonic anhydride) and in the presence of a suitable solvent (such as THF) and a suitable base (such as an amine base, e.g. N,N-diisopropylethylamine); or
  • (v) for compounds of formula I wherein at least one R³ group is present and represents an alkyl, aryl, heteroaryl or heterocycloalkyl group, reaction of a corresponding compound of formula I but wherein the relevant R³ group instead represents LG¹, wherein LG¹ represents a suitable leaving group (such as halo, e.g. Br), with a compound of formula VII

• • wherein R³ is as defined herein and LG² represents a suitable leaving group (such as a suitable boronic ester), in the presence of a suitable catalyst (such as a Pd catalyst, e.g. Pd(PPh₃)₄), and in the presence of a suitable solvent (such as a mixture of 1,4-dioxane and water) and a suitable base (such an inorganic base, e.g. K₂CO₃).

Compounds of formulas II, III, IV, V, VI and VII are either commercially available, are known in the literature, or may be obtained either by analogy with the processes described herein, or by conventional synthetic procedures, in accordance with standard techniques, from available starting materials using appropriate reagents and reaction conditions. In this respect, the skilled person may refer to inter alia “Comprehensive Organic Synthesis” by B. M. Trost and I. Fleming, Pergamon Press, 1991. Further references that may be employed include “Heterocyclic Chemistry” by J. A. Joule, K. Mills and G. F. Smith, 3^rd edition, published by Chapman & Hall, “Comprehensive Heterocyclic Chemistry II” by A. R. Katritzky, C. W. Rees and E. F. V. Scriven, Pergamon Press, 1996 and “Science of Synthesis”, Volumes 9-17 (Hetarenes and Related Ring Systems), Georg Thieme Verlag, 2006.

The skilled person will understand that the substituents as defined herein, and substituents thereon, may be modified one or more times, after or during the processes described above for the preparation of compounds of the invention by way of methods that are well known to those skilled in the art. Examples of such methods include substitutions, reductions, oxidations, dehydrogenations, alkylations, dealkylations, acylations, hydrolyses, esterifications, etherifications, halogenations and nitrations. The precursor groups can be changed to a different such group, or to the groups defined in formula I, at any time during the reaction sequence. The skilled person may also refer to “Comprehensive Organic Functional Group Transformations” by A. R. Katritzky, O. Meth-Cohn and C. W. Rees, Pergamon Press, 1995 and/or “Comprehensive Organic Transformations” by R. C. Larock, Wiley-VCH, 1999.

Compounds of the invention may be isolated from their reaction mixtures and, if necessary, purified using conventional techniques as known to those skilled in the art. Thus, processes for preparation of compounds of the invention as described herein may include, as a final step, isolation and optionally purification of the compound of the invention.

It will be appreciated by those skilled in the art that, in the processes described above and hereinafter, the functional groups of intermediate compounds may need to be protected by protecting groups. The protection and deprotection of functional groups may take place before or after a reaction in the above-mentioned schemes.

Protecting groups may be applied and removed in accordance with techniques that are well-known to those skilled in the art and as described hereinafter. For example, protected compounds/intermediates described herein may be converted chemically to unprotected compounds using standard deprotection techniques. The type of chemistry involved will dictate the need, and type, of protecting groups as well as the sequence for accomplishing the synthesis. The use of protecting groups is fully described in “Protective Groups in Organic Synthesis”, 3rd edition, T. W. Greene & P. G. M. Wutz, Wiley-Interscience (1999), the contents of which are incorporated herein by reference.

Compounds of the invention may have the advantage that they may be more efficacious than, be less toxic than, be longer acting than, be more potent than, produce fewer side effects than, be more easily absorbed than, and/or have a better pharmacokinetic profile (e.g. higher oral bioavailability and/or lower clearance) than, and/or have other useful pharmacological, physical, or chemical properties over, compounds known in the prior art, whether for use in the above-stated indications or otherwise. In particular, compounds of the invention may have the advantage that they are more efficacious and/or exhibit advantageous properties in vivo.

EXAMPLES

The present invention will be further described by reference to the following examples, which are not intended to limit the scope of the invention.

In the event that there is a discrepancy between nomenclature and any compounds depicted graphically, then it is the latter that presides (unless contradicted by any experimental details that may be given or unless it is clear from the context).

Experimental Procedures

Starting materials and intermediates used in the synthesis of compounds described herein are commercially available or can be prepared by the methods described herein or by methods known in the art.

Where necessary, experiments were carried out in dry conditions and/or under inert atmosphere (nitrogen or argon), particularly in cases where oxygen- or moisture-sensitive reagents or intermediates were used.

Mass spectrometry data are reported from liquid chromatography-mass spectrometry (LC-MS) using electrospray ionization. Chemical shifts for NMR data are expressed in parts per million (ppm, δ) referenced to residual peaks from the deuterated solvent used.

For syntheses referencing general procedures, reaction conditions (such as length of reaction or temperature) may vary. In general, reactions were followed by thin layer chromatography or LC-MS, and subjected to work-up when appropriate. Purifications may vary between experiments: in general, solvents and the solvent ratios used for eluents/gradients were chosen to provide an appropriate R_f and/or retention time.

General Procedures

Processes used in the synthesis of compounds as described in the following examples may be represented by the following general procedures, wherein variable groups indicated (such as R¹, R², X, and the like) may have meanings distinct from those indicated in the first aspect of the invention.

General procedure A: A mixture of the corresponding nitrobenzene compound (1.0 equiv.), a suitable amine (1.1 equiv.), and N,N-diisopropylethylamine (1.2 equiv.) was stirred in 2-propanol at 120° C. for 12-72 h. Thereafter, the mixture was poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried (using MgSO₄), filtered, concentrated, and purified by silica gel chromatography.

General procedure B: To a mixture of a substituted 2-amino-1-nitrobenzene compound (1.0 equiv.) and NiCl₂ (0.20 equiv.) in acetonitrile/water (9:1 v/v) was added NaBH₄ (4.0 equiv.) portion wise. After complete reaction, DCM was added and the liquids were poured into NaHCO₃ by means of decantation. The aqueous phase was extracted with DCM×3 and the combined extracts were dried (using MgSO₄) and filtered. To the filtrate was then added N,N-diisopropylethylamine (2.2 equiv.) and diphosgene (0.50 equiv.) or triphosgene (0.34 equiv.). After complete reaction, the mixture was concentrated and purified by silica gel chromatography.

General procedure C: The corresponding tert-butyl carbamate compound was dissolved in DCM, then trifluoroacetic acid (5-15 equiv.) was added and the mixture was stirred at 20° C. for 10-60 min. After complete reaction, the solvents were removed by co-evaporation with 2-propanol. Unless otherwise stated, no further purification was done.

General procedure D: A mixture of the corresponding amine or trifluoroacetate salt thereof (1.0 equiv.) and N,N-diisopropylethylamine (2.0 equiv.) was stirred in DCM, then a suitable isocyanate or isothiocyanate (1.0 equiv.) was added and the resulting mixture was stirred at 50° C. for 3-16 h. After complete reaction the mixture was purified by silica gel chromatography or by preparative liquid chromatography.

General procedure E: A mixture of the corresponding 4-bromobenzimidazolone (1.0 equiv.), a suitable organoboronic acid or pinacol boronic acid ester (1.2 equiv.), K₂CO₃ (2.5 equiv.), and Pd(PPh₃)₄ (0.030 equiv.) in 1,4-dioxane and water (5:1 v/v mixture) was stirred at 100° C. for 2-72 h. After complete reaction, the mixture was poured into NaHCO₃ (sat.) and extracted with DCM×3. The combined organics were concentrated and the crude material was purified by silica gel chromatography or by preparative liquid chromatography.

General procedure F: A mixture of the corresponding nitrobenzene compound (1.0 equiv.) and Pd/C (0.05 equiv.) was stirred in THE at 20° C. for 12-24 h under an H₂ atmosphere provided by a balloon. After complete reaction the balloon was removed and N,N-diisopropylethylamine (2.0 equiv.) and triphosgene (0.35 equiv.) were added. The resulting mixture was stirred for 20-60 min at 20° C. and was then filtered, concentrated, and purified by silica gel chromatography.

General procedure G: A mixture of the corresponding benzyl protected compound (1 equiv.) and Pd/C (0.1 equiv.) was stirred in 1,4-dioxane and cyclohexene (10:1 v/v) in a sealed vial at 120° C. for 2-16 h. Upon complete reaction the mixture was filtered, concentrated, and purified by silica gel chromatography.

General procedure H: A mixture of the corresponding carboxylic acid (1.0 equiv.), an appropriate amine (2 equiv.), propylphosphonic anhydride (4 equiv.) and N,N-diisopropylethylamine (3.0 equiv.) was stirred in THE or acetonitrile at an elevated temperature for 3-16 h. After complete reaction the mixture was purified by silica gel chromatography or by preparative liquid chromatography.

General procedure 1: To a mixture of a suitable amine or a salt thereof (1.0 equiv.) and N,N-diisopropylethylamine (2.0 equiv.) in DCM was added diphosgene (0.50 equiv.) under vigorous stirring. The mixture was stirred at 20° C. for 5-15 min after which it was added to a separate mixture of the corresponding amine or a salt thereof (1.0 equiv.) and N,N-diisopropylethylamine (2.0 equiv.) in DCM. The resulting mixture was stirred at 50° C. for 3-16 h. After complete reaction the mixture was purified by silica gel chromatography or by preparative liquid chromatography.

General procedure J: A mixture of the corresponding ester (1.0 equiv.) and LiOH (5.0 equiv.) was stirred in MeOH and water (3:1 v/v) at 20° C. for 5-24 h. After complete reaction the mixture poured into aqueous HCl (2 M) and extracted with DCM×3. The combined organics were concentrated and purified by silica gel chromatography.

General procedure K: A mixture of the corresponding reactant (1.0 equiv.) and NaH (1.1 equiv.) was stirred in THF at 20° C. for 20 min. Then a substituted 1-fluoro-2-nitrobenzene compound (1.0 equiv.) was added and the resulting mixture was stirred at elevated temperatures. Upon completion of the reaction, the mixture was poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried (using MgSO₄), filtered, concentrated, and purified by silica gel chromatography.

General procedure L: A sealable, two-chamber reaction vessel that allows for gas exchange between the two chambers was used. Chamber 1 was charged with a magnetic stirring bar, the appropriate aryl bromide (1.0 equiv.), the appropriate amine (1.5 equiv.), Pd(PPh₃)₄ or Pd(dppf)Cl₂ (0.050 equiv.), diisopropylethylamine (3 equiv.), and dioxane. Chamber 2 was charged with a magnetic stirring bar, Mo(CO)₆ (2.0 equiv.) and dioxane. The two-chamber reaction vial was then sealed and flushed with nitrogen for 3-5 min. Thereafter DBU (2.1 equiv.) was injected into chamber 2. Both chambers were then heated to 70° C. and the reaction mixtures were stirred 16-48 h. After cooling the reaction mixture, the seal was punctured with a needle to release excess carbon monoxide before opening the seal. The reaction mixture was then poured into HCl (2M) and extracted with DCM×3, the combined organics were then dried (MgSO₄) and concentrated. The crude mixture was purified by preparative HPLC or by silica gel chromatography.

General procedure M: A mixture of the appropriate 2-fluoronitrobenzene compound (1.0 equiv.) and the appropriate amine (3-5 equiv.) was stirred at 120° C. for 16-72 h. The mixture was then poured into HCl (2 M) and extracted with DCM×3. The combined organics were concentrated and purified by silica gel chromatography.

General procedure N: A mixture of the appropriate 2-fluoronitrobenzene compound (1.0 equiv.), the appropriate alcohol, and Cs₂CO₃ in DMF was stirred at 60° C. overnight. The mixture was then diluted with methanol, filtered, and purified by preparative HPLC.

General procedure O: A mixture of an appropriate amine (1.0 equiv.), an appropriate carboxylic acid (1.3 equiv.), HATU (1.5 equiv.) and triethylamine (3 equiv.) in DMF was stirred at r.t. for 16-24 h. The mixture was then diluted with methanol, filtered and purified by preparative HPLC.

Synthesis of Intermediates

Intermediate 1: 4-Bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-bromo-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-bromo-3-fluoro-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺344.

Step 2: tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-bromo-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺340. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 7.76 (s, 1H), 7.18-7.21 (m, 1H), 7.05-7.09 (m, 1H), 6.94-6.99 (m, 1H), 4.45 (tt, J=12.5, 3.9 Hz, 1H), 4.27-4.37 (m, 2H), 2.86 (m, 2H), 2.28 (m, 2H), 1.83 (m, 2H), 1.51 (s, 9H).

Step 3: 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 296. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.38 (s, 1H), 8.57-8.70 (m, 1H), 8.31-8.47 (m, 1H), 7.32 (d, J=8.1 Hz, 1H), 7.21 (dd, J=8.1, 0.9 Hz, 1H), 7.01 (t, J=8.1 Hz, 1H), 4.53 (tt, J=12.2, 4.5 Hz, 1H), 3.45 (br. s., 2H), 3.02-3.16 (m, 2H), 2.52-2.61 (m, 2H), 1.84-1.93 (m, 2H).

Intermediate 2: 4-Chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-chloro-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-chloro-3-fluoro-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺300.

Step 2: tert-butyl 4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-chloro-2-nitro-anilino)piperidine-1-carboxylate. 1H-NMR (400 MHz, CHLOROFORM-d) δ ppm 7.80 (br. s., 1H), 6.97-7.09 (m, 3H), 4.45 (tt, J=12.5, 4.1 Hz, 1H), 4.32 (m, 2H), 2.82-2.91 (m, 2H), 2.28 (m, 2H), 1.83 (m, 2H), 1.51 (s, 9H).

Step 3: 4-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 232.

Intermediate 3: 4-Fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺284.

Step 2: tert-butyl 4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺280. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.19 (s, 1H), 6.97-7.04 (m, 1H), 6.91-6.94 (m, 1H), 6.82-6.87 (m, 1H), 4.47 (tt, J=12.5, 4.2 Hz, 1H), 4.33 (m, 2H), 2.82-2.92 (m, 2H), 2.29 (m, 2H), 1.84 (m, 2H), 1.51 (s, 9H).

Step 3: 4-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 236. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.52 (s, 1H), 8.89 (br. s., 1H), 8.65 (br. s., 1H), 7.19 (d, J=7.9 Hz, 1H), 7.02 (td, J=8.1, 5.4 Hz, 1H), 6.88-6.96 (m, 1H), 4.54 (m, 1H), 3.04-3.17 (m, 2H), 2.53-2.61 (m, 2H), 1.88 (m, 2H).

Intermediate 4: 4-Methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-methyl-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-fluoro-3-methyl-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 336.

Step 2: (tert-butyl 4-(4-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure F from tert-butyl 4-(3-methyl-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺276.

Step 3: 4-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 232. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.00 (br. s., 1H), 8.71 (br. s, 1H), 8.47 (br. s, 1H), 7.11-7.18 (m, 1H), 6.90-6.97 (m, 1H), 6.80-6.86 (m, 1H), 4.46-4.57 (m, 1H), 3.38-3.49 (m, 2H), 3.03-3.18 (m, 2H), 2.53-2.63 (m, 2H), 2.28 (s, 3H), 1.80-1.91 (m, 2H).

Intermediate 5: 4-Methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-methoxy-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-fluoro-3-methoxy-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate.

Step 2: tert-butyl 4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure F from tert-butyl 4-(3-methoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺292.

Step 3: 4-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 248. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.03 (s, 1H), 8.66 (br. s., 1H), 8.43 (br. s, 1H), 6.94-7.03 (m, 2H), 6.68-6.77 (m, 1H), 4.50 (br. t, J=11.7, 11.7 Hz, 1H), 3.85 (s, 3H), 3.45 (br. s., 2H), 3.03-3.17 (m, 2H), 2.53-2.61 (m, 2H), 1.79-1.89 (m, 2H).

Intermediate 6: 4-Hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: A mixture of 3-fluoro-2-nitro-phenol (1.0 equiv.), tert-butyl-chloro-dimethyl-silane (1.1 equiv.), and imidazole (2.0 equiv.) in DMF was stirred at 20° C. for 16 h. The mixture was then poured into water and extracted with Et₂O×3. The combined organics were dried and concentrated. The crude tert-butyl-(3-fluoro-2-nitro-phenoxy)-dimethyl-silane was used without further purification in step 2. LCMS [M+H]⁺ 272.

Step 2: tert-butyl 4-[3-[tert-butyl(dimethyl)silyl]oxy-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from tert-butyl-(3-fluoro-2-nitro-phenoxy)-dimethyl-silane and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-(TBDMS)-isobutene+H]⁺282.

Step 3: tert-butyl 4-{4-[(tert-butyldimethylsilyl)oxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate was synthesized according to General procedure F from tert-butyl 4-[3-[tert-butyl(dimethyl)silyl]oxy-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M−H]⁻ 446.

Step 4: Synthesis of tert-butyl 4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. A mixture of tert-butyl 4-[4-[tert-butyl(dimethyl)silyl]oxy-2-oxo-3H-benzimidazol-1-yl]piperidine-1-carboxylate (1.0 equiv.) and LiOH (6.0 equiv.) was stirred in DMF at 80° C. for 4 h. The mixture was then poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried, concentrated, and purified by silica gel chromatography. LCMS [M-isobutene+H]⁺278. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.64 (br. s., 1H), 9.62 (br. s., 1H), 6.75-6.81 (m, 1H), 6.65 (dd, J=8.1, 0.8 Hz, 1H), 6.48 (dd, J=8.1, 0.8 Hz, 1H), 4.23-4.33 (m, 1H), 4.01-4.14 (m, 2H), 2.85 (br. s., 2H), 2.16 (m, 2H), 1.60-1.69 (m, 2H), 1.43 (s, 9H).

Step 5: 4-hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 234.

Intermediate 7: 5-Fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(4-fluoro-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1,4-difluoro-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺284.

Step 2: tert-butyl 4-(5-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(4-fluoro-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺280. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.32 (s, 1H), 7.03 (dt, J=8.4, 4.0 Hz, 1H), 6.75-6.86 (m, 2H), 4.45 (tt, J=12.6, 4.0 Hz, 1H), 4.33 (m, 2H), 2.82-2.92 (m, 2H), 2.28 (m, 2H), 1.79-1.88 (m, 2H), 1.51 (s, 9H).

Step 3: 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(5-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 236. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.56 (br. s., 1H), 8.35 (br. s., 1H), 7.27 (dd, J=8.5, 4.4 Hz, 1H), 6.86-6.94 (m, 2H), 4.46-4.55 (m, 1H), 3.44 (m, 2H), 3.03-3.14 (m, 2H), 2.45-2.58 (overlapping m, 2H), 1.83-1.90 (m, 2H).

Intermediate 8: 5-Methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(4-methoxy-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-fluoro-4-methoxy-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate.

Step 2: tert-butyl 4-(5-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure F from tert-butyl 4-(4-methoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺292.

Step 3: 5-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(5-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 248. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.85 (s, 1H), 8.57-8.69 (m, 1H), 8.33-8.48 (m, 1H), 7.19 (d, J=8.5 Hz, 1H), 6.63 (dd, J=8.5, 2.4 Hz, 1H), 6.60 (d, J=2.4 Hz, 1H), 4.47 (tt, J=12.3, 4.5 Hz, 1H), 3.73 (s, 3H), 3.38-3.48 (m, 2H), 3.02-3.16 (m, 2H), 2.45-2.58 (overlapping m, 2H), 1.79-1.89 (m, 2H).

Intermediate 9: 2-Oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazole-5-carbonitrile;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(4-cyano-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 4-fluoro-3-nitro-benzonitrile and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺291.

Step 2: tert-butyl 4-(5-cyano-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure F from tert-butyl 4-(4-cyano-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M+H]⁺ 343. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 9.36 (br. s., 1H), 7.41 (dd, J=8.5, 1.6 Hz, 1H), 7.36-7.38 (m, 1H), 7.20 (d, J=8.2 Hz, 1H), 4.48 (tt, J=12.5, 4.1 Hz, 1H), 4.35 (m, 2H), 2.88 (m, 2H), 2.30 (m, 2H), 1.85 (m, 2H), 1.52 (s, 9H).

Step 3: 2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazole-5-carbonitrile;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(5-cyano-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 243. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.45 (s, 1H), 8.79 (br. s., 1H), 8.40-8.58 (m, 1H), 7.54-7.58 (m, 1H), 7.46-7.51 (m, 1H), 7.43 (d, J=1.6 Hz, 1H), 4.52-4.63 (m, 1H), 3.44 (m, 2H), 3.09 (m, 2H), 2.47-2.60 (m, 2H), 1.89 (m, 2H).

Intermediate 10: 4-(Methylsulfanyl)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-methylsulfanyl-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure K from tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate and sodium methylthiolate. LCMS [M+H]⁺ 368.

Step 2: tert-butyl 4-(4-methylsulfanyl-2-oxo-3H-benzimidazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-methylsulfanyl-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M+H]⁺ 364. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 7.89 (s, 1H), 7.09-7.13 (m, 1H), 7.02-7.08 (m, 2H), 4.46 (tt, J=12.5, 4.1 Hz, 1H), 4.28-4.37 (m, 2H), 2.82-2.90 (m, 2H), 2.48 (s, 3H), 2.23-2.36 (m, 2H), 1.83 (m, 2H), 1.51 (s, 9H).

Step 3:4-(methylsulfanyl)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-methylsulfanyl-2-oxo-3H-benzimidazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 264. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.12 (s, 1H), 8.59 (br. s., 1H), 8.38 (br. s., 1H), 7.20 (dd, J=7.3, 0.9 Hz, 1H), 7.05 (t, J=7.7 Hz, 1H), 7.00-7.03 (m, 1H), 4.51 (ddt, J=12.4, 8.3, 4.1, 4.1 Hz, 1H), 3.40-3.48 (m, 2H), 3.03-3.16 (m, 2H), 2.45-2.62 (overlapping m, 2H), 1.82-1.91 (m, 2H).

Intermediate 11: 4-amino-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: N,N-dibenzyl-3-fluoro-2-nitro-aniline was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and N-benzyl-1-phenylmethanamine.

LCMS [M+H]⁺ 337. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.22-7.36 (m, 11H), 6.83-6.90 (m, 2H), 4.20 (s, 4H).

Step 2: tert-butyl 4-{[3-(dibenzylamino)-2-nitrophenyl]amino}piperidine-1-carboxylate was synthesized according to General procedure A from N,N-dibenzyl-3-fluoro-2-nitro-aniline and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 517. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 7.18-7.32 (m, 10H), 7.13 (t, J=8.2 Hz, 1H), 6.61 (d, J=8.2 Hz, 1H), 6.55 (d, J=7.3 Hz, 1H), 5.51 (d, J=7.9 Hz, 1H), 4.04 (s, 4H), 3.82-3.93 (m, 2H), 3.42-3.53 (m, 1H), 2.82 (br. s., 2H), 1.75-1.84 (m, 2H), 1.39 (s, 9H), 1.27-1.36 (m, 2H).

Step 3: tert-butyl 4-[4-(dibenzylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-{[3-(dibenzylamino)-2-nitrophenyl]amino}piperidine-1-carboxylate. LCMS [M+H]⁺ 513. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.24-7.39 (overlapping m, 10H), 6.93 (s, 1H), 6.80-6.86 (m, 1H), 6.71-6.76 (m, 1H), 4.17-4.46 (m, 7H), 2.74-2.90 (m, 2H), 2.16-2.33 (m, 2H), 1.70-1.82 (m, 2H), 1.50 (s, 9H).

Step 4: tert-butyl 4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure G from tert-butyl 4-[4-(dibenzylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate.

LCMS [M+H]⁺ 333. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.24 (br. s., 1H), 6.72 (t, J=7.9 Hz, 1H), 6.55 (d, J=7.9 Hz, 1H), 6.30 (dd, J=7.9, 0.6 Hz, 1H), 4.86-4.93 (m, 2 H), 4.15 (tt, J=12.3, 4.3 Hz, 1H), 2.98-3.08 (m, 2H), 2.49-2.58 (overlapping m, 2H), 2.09-2.21 (m, 2H), 1.50-1.58 (m, 2H).

Step 5: The title compound was synthesized according to General procedure C from tert-butyl 4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate.

LCMS [M+H]⁺ 233. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.35 (s, 1H), 8.56-8.66 (m, 1H), 8.38 (br. s., 1H), 6.78 (t, J=8.1 Hz, 1H), 6.63 (d, J=8.1 Hz, 1H), 6.34-6.38 (m, 1H), 4.40-4.50 (m, 1H), 3.39-3.45 (m, 2H), 3.17 (s, 2H), 3.04-3.15 (m, 3H), 2.47-2.60 (overlapping m, 2H), 1.79-1.87 (m, 2H).

Intermediate 12: 4-(Methylamino)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: N-benzyl-3-fluoro-N-methyl-2-nitroaniline was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and N-methyl-1-phenylmethanamine.

LCMS [M+H]⁺ 261.

Step 2: tert-butyl 4-[3-[benzyl(methyl)amino]-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from N-benzyl-3-fluoro-N-methyl-2-nitroaniline and tert-butyl 4-aminopiperidine-1-carboxylate.

Step 3: tert-butyl 4-{4-[benzyl(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-[benzyl(methyl)amino]-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 437.

Step 4: tert-butyl 4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure G from tert-butyl 4-{4-[benzyl(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate.

LCMS [M+H]⁺ 347. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 10.51-10.65 (m, 1H), 7.02 (td, J=8.1, 0.9 Hz, 1H), 6.69 (dd, J=7.9, 3.8 Hz, 1H), 6.50-6.56 (m, 1H), 4.45 (tt, J=12.4, 4.0 Hz, 1H), 4.32 (br. s., 2H), 3.00 (d, J=1.6 Hz, 3H), 2.88 (br. s., 2H), 2.34 (m, 2H), 1.79-1.86 (m, 2H), 1.51 (s, 9H).

Step 5: The title compound was synthesized according to General procedure C from tert-butyl 4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 247. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.57-8.67 (m, 1H), 8.33-8.44 (m, 1H), 6.90 (t, J=7.9 Hz, 1H), 6.68 (d, J=7.9 Hz, 1H), 6.30 (d, J=7.9 Hz, 1H), 4.46 (tt, J=12.4, 3.9 Hz, 1H), 3.38-3.47 (m, 2H), 3.04-3.16 (m, 2H), 2.80 (s, 3H), 2.47-2.60 (overlapping m, 2H), 1.79-1.87 (m, 2H).

Intermediate 13: 4-(Dimethylamino)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: 3-fluoro-N,N-dimethyl-2-nitro-aniline was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and dimethylammonium chloride. LCMS [M+H]⁺ 185.

Step 2: tert-butyl 4-[3-(dimethylamino)-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from 3-fluoro-N,N-dimethyl-2-nitro-aniline and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 365.

Step 3: tert-butyl 4-[4-(dimethylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-(dimethylamino)-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 361. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 7.01-7.06 (m, 1H), 6.89 (br. s., 1H), 6.77 (br. d, J=9.2 Hz, 1H), 4.46 (tt, J=12.6, 4.0 Hz, 1H), 4.32 (br. s., 2H), 2.81-2.94 (m, 6H), 2.31 (m, 2H), 1.79-1.87 (m, 2H), 1.55-1.63 (m, 2H), 1.51 (s, 9H).

Step 4: The title compound was synthesized according to General procedure C from tert-butyl 4-[4-(dimethylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 261.

Intermediate 14: 4-Ethoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: In a flask, sodium (3.6 equiv.) was added to ethanol and the resulting mixture was stirred until all sodium had reacted. Then, tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate (1.0 equiv.) was added, and the resulting mixture was stirred at 120° C. for 16 h. Thereafter the mixture was poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried (MgSO₄), concentrated, and purified by silica gel chromatography which afforded tert-butyl 4-(3-ethoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺310.

Step 2: tert-butyl 4-(4-ethoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-ethoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M+H]⁺ 362.

Step 3: The title compound was synthesized according to General procedure C from tert-butyl 4-(4-ethoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate.

LCMS [M+H]⁺ 262. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.98 (s, 1H), 8.67 (br. s., 1H), 8.45 (br. s., 1H), 6.94-6.98 (m, 2H), 6.69-6.74 (m, 1H), 4.50 (tt, J=12.3, 4.3 Hz, 1H), 4.13 (q, J=7.0 Hz, 2H), 3.40-3.47 (m, 2H), 3.03-3.17 (m, 2H), 2.45-2.61 (overlapping m, 2H), 1.80-1.89 (m, 2H), 1.35 (t, J=7.0 Hz, 3H).

Intermediate 15: Methyl 2-[2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-4-yl]acetate;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-[3-(2-methoxy-2-oxo-ethyl)-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from methyl 2-(3-fluoro-2-nitro-phenyl)acetate and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 394.

Step 2: tert-butyl 4-[4-(2-methoxy-2-oxoethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-(2-methoxy-2-oxo-ethyl)-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺334. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.56 (br. s., 1H), 6.98-7.09 (m, 2H), 6.92 (d, J=7.6 Hz, 1H), 4.47 (tt, J=12.4, 4.0 Hz, 1H), 4.32 (m, 2H), 3.73 (s, 3H), 3.70 (s, 2H), 2.87 (m, 2H), 2.31 (m, 2H), 1.83 (m, 2H), 1.51 (s, 9H).

Step 3: The title compound was synthesized according to General procedure C from tert-butyl 4-[4-(2-methoxy-2-oxoethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 290.

Intermediate 16: 5-Methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-[(4-methyl-2-nitrophenyl)amino]piperidine-1-carboxylate was synthesized according to General procedure A from 1-fluoro-4-methyl-2-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 336.

Step 2: tert-butyl 4-(5-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[(4-methyl-2-nitrophenyl)amino]piperidine-1-carboxylate. LCMS [M+H]⁺ 332. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.47 (s, 1H), 7.02 (d, J=8.2 Hz, 1H), 6.85-6.93 (m, 2H), 4.46 (tt, J=12.5, 3.9 Hz, 1H), 4.32 (m, 2H), 2.81-2.93 (m, 2H), 2.38 (s, 3H), 2.31 (m, 2H), 1.83 (m, 2H), 1.51 (s, 9H).

Step 3: The title compound was synthesized according to General procedure C from tert-butyl 4-(5-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate.

LCMS [M+H]⁺ 232.

¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.83 (s, 1H), 8.75 (br. s., 1H), 8.44-8.60 (m, 1H), 7.19 (d, J=8.5 Hz, 1H), 6.79-6.86 (m, 2H), 4.45-4.55 (m overlap w water, 1H), 3.43 (m, 2H), 3.10 (m, 2H), 2.46-2.59 (m overlap w DMSO, 2H), 2.30 (s, 3H), 1.84 (m, 2H).

Intermediate 17: 7-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(2-fluoro-6-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1,2-difluoro-3-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺284.

Step 2: tert-butyl 4-(7-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(2-fluoro-6-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺280.

Step 3: 7-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(7-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 236.

Intermediate 18: 7-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(2-chloro-6-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-chloro-2-fluoro-3-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺300.

Step 2: tert-butyl 4-(7-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(2-chloro-6-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺296.

Step 3: 7-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(7-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 252.

Intermediate 19: 7-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(2-bromo-6-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-bromo-2-fluoro-3-nitrobenzene and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M-isobutene+H]⁺344.

Step 2: tert-butyl 4-(7-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(2-bromo-6-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺340.

Step 3: 7-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(7-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 296.

Intermediate 20: 1-(Piperidin-4-yl)-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: 1-(3-fluoro-2-nitro-phenyl)-1,2,4-triazole was synthesized according to General procedure K from 1,3-difluoro-2-nitrobenzene and 1,2,4-triazole. LCMS [M+H]⁺ 209. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 9.01 (s, 1H), 8.19 (s, 1H), 7.79-7.86 (m, 1H), 7.69 (dt, J=8.2, 1.3 Hz, 1H), 7.63 (ddd, J=9.6, 8.7, 1.3 Hz, 1H).

Step 2: tert-butyl 4-[2-nitro-3-(1,2,4-triazol-1-yl)anilino]piperidine-1-carboxylate was synthesized according to General procedure A from 1-(3-fluoro-2-nitro-phenyl)-1,2,4-triazole and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 389.

Step 3: tert-butyl 4-[2-oxo-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[2-nitro-3-(1,2,4-triazol-1-yl)anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 385.

¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 9.29 (br. s., 1H), 8.78 (s, 1H), 8.19 (s, 1H), 7.07-7.26 (m, 3H), 4.51 (tt, J=12.5, 4.1 Hz, 1H), 4.35 (m, 2H), 2.88 (m, 2H), 2.33 (m, 2H), 1.86 (m, 2H), 1.52 (s, 9H).

Step 4: The title compound was synthesized according to General procedure C from tert-butyl 4-[2-oxo-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 285.

Intermediate 21: 1-(Piperidin-4-yl)-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: 1-(3-fluoro-2-nitro-phenyl)pyrazole was synthesized according to General procedure K from 1,3-difluoro-2-nitrobenzene and pyrazole. LCMS [M+H]⁺ 208.

Step 2: tert-butyl 4-(2-nitro-3-pyrazol-1-yl-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from 1-(3-fluoro-2-nitro-phenyl)pyrazole and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 388. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 7.68-7.73 (m, 1H), 7.40 (dd, J=8.7, 7.7 Hz, 1H), 6.85-6.89 (m, 1H), 6.74 (dd, J=7.7, 1.1 Hz, 1H), 6.47 (dd, J=2.5, 1.9 Hz, 1H), 4.03 (m, 2H), 3.55-3.65 (m, 1H), 3.02 (m, 2H), 2.00-2.09 (m, 2H), 1.48 (s, 9H).

Step 3: tert-butyl 4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(2-nitro-3-pyrazol-1-yl-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺328.

Step 4: The title compound was synthesized according to General procedure C from tert-butyl 4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 284.

Intermediate 22: 4-(4-Bromo-1H-pyrazol-1-yl)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: 4-bromo-1-(3-fluoro-2-nitro-phenyl)pyrazole was synthesized according to General procedure K from 1,3-difluoro-2-nitrobenzene and 4-bromo-1H-pyrazol.

Step 2: tert-butyl 4-[3-(4-bromopyrazol-1-yl)-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from 4-bromo-1-(3-fluoro-2-nitro-phenyl)pyrazole and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 466.

Step 3: tert-butyl 4-[4-(4-bromo-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-(4-bromopyrazol-1-yl)-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 462.

Step 4: The title compound was synthesized according to General procedure C from tert-butyl 4-[4-(4-bromo-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 362. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.88 (s, 1H), 8.66 (d, J=0.6 Hz, 1H), 8.60 (br. s., 1H), 8.37 (br. s, 1H), 7.90 (d, J=0.6 Hz, 1H), 7.35 (m, 2H), 7.19 (dd, J=8.5, 7.6 Hz, 1H), 4.52-4.63 (m, 2H), 3.03-3.17 (m, 2H), 2.59 (m, 2H), 1.87-1.95 (m, 2H).

Intermediate 23: 1-(1-(1-((4-Iodophenyl)carbamoyl)piperidin-4-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)-1H-pyrazole-4-carboxylic acid

Step 1: ethyl 1-(3-fluoro-2-nitro-phenyl)pyrazole-4-carboxylate was synthesized according to General procedure K from 1,3-difluoro-2-nitrobenzene and ethyl 1H-pyrazole-4-carboxylate. LCMS [M+H]⁺ 280. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.27 (d, J=0.6 Hz, 1H), 8.11 (d, J=0.6 Hz, 1H), 7.64 (td, J=8.5, 5.4 Hz, 1H), 7.34-7.42 (m, 2H), 4.35 (q, J=7.1 Hz, 2H), 1.38 (t, J=7.1 Hz, 3H).

Step 2: tert-butyl 4-[3-(4-ethoxycarbonylpyrazol-1-yl)-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from ethyl 1-(3-fluoro-2-nitro-phenyl)pyrazole-4-carboxylate and tert-butyl 4-aminopiperidine-1-carboxylate.

LCMS [M-isobutene+H]⁺404. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.17 (d, J=0.6 Hz, 1H), 8.07 (d, J=0.6 Hz, 1H), 7.42 (dd, J=8.7, 7.7 Hz, 1H), 6.93 (dd, J=9.3, 1.1 Hz, 1H), 6.72 (dd, J=7.6, 1.3 Hz, 1H), 4.34 (q, J=7.2 Hz, 2H), 4.04 (m, 2H), 3.56-3.67 (m, 1H), 3.02 (m, 2H), 2.00-2.09 (m, 2H), 1.48 (m, 11H), 1.37 (t, J=7.2 Hz, 3H).

Step 3: tert-butyl 4-{4-[4-(ethoxycarbonyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-(4-ethoxycarbonylpyrazol-1-yl)-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 456. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 9.47 (br. s, 1H), 8.53 (s, 1H), 8.13 (s, 1H), 7.19 (dd, J=7.9, 1.3 Hz, 1H), 7.13 (t, J=8.1 Hz, 1H), 7.07-7.10 (m, 1H), 4.51 (tt, J=12.5, 4.1 Hz, 1H), 4.29-4.40 (m, 4H), 2.88 (m, 2H), 2.33 (m, 2H), 1.82-1.89 (m, 2H), 1.52 (s, 9H), 1.40 (t, J=7.1 Hz, 3H).

Step 4: Ethyl 1-[2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-4-yl]-1H-pyrazole-4-carboxylate was synthesized according to General procedure C from tert-butyl 4-{4-[4-(ethoxycarbonyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate. LCMS [M+H]⁺ 356. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.95 (s, 1H), 8.94 (s, 1H), 8.69 (br. s., 1H), 8.46 (br. s., 1H), 8.15 (s, 1H), 7.46 (d, J=7.9 Hz, 1H), 7.39 (d, J=7.6 Hz, 1H), 7.16-7.23 (m, 1H), 4.54-4.64 (m, 1H), 4.29 (q, J=7.0 Hz, 2H), 3.42-3.51 (m, 2H), 3.04-3.18 (m, 2H), 2.54-2.69 (m, 2H), 1.86-1.97 (m, 2H), 1.32 (t, J=7.0 Hz, 3H).

Step 5: Ethyl 1-[1-[1-[(4-iodophenyl)carbamoyl]-4-piperidyl]-2-oxo-3H-benzimidazol-4-yl]pyrazole-4-carboxylate was synthesized according to general procedure D from ethyl 1-[2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-4-yl]-1H-pyrazole-4-carboxylate. LCMS [M+H]⁺ 601.

Step 6: The title compound was synthesized according to general procedure J from ethyl 1-[1-[1-[(4-iodophenyl)carbamoyl]-4-piperidyl]-2-oxo-3H-benzimidazol-4-yl]pyrazole-4-carboxylate. LCMS [M+H]⁺ 573.

Intermediate 24: 1-(Piperidin-4-yl)-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure E from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate and 3-pyridylboronic acid. LCMS [M+H]⁺ 395. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 9.51 (br. s., 1H), 8.89 (s, 1H), 8.73 (d, J=3.8 Hz, 1H), 8.05 (d, J=7.6 Hz, 1H), 7.57-7.63 (m, 1H), 7.22 (s, 1H), 7.21 (s, 1H), 7.10-7.14 (m, 1H), 4.48 (tt, J=12.4, 4.1 Hz, 1H), 4.35 (br. s., 2H), 2.90 (br. s., 2H), 2.27-2.42 (m, 2H), 1.86 (m, 2H), 1.53 (s, 9H).

Step 2: The title compound was synthesized according to General procedure C from tert-butyl 4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 295. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.24 (br. s., 1H), 8.85 (br. s., 1H), 8.71 (br. s., 1H), 8.64 (br. s, 1H), 8.32-8.49 (m, 1H), 8.13-8.21 (m, 1H), 7.67-7.73 (m, 1H), 7.39-7.44 (m, 1H), 7.18-7.24 (m, 1H), 7.11-7.17 (m, 1H), 4.53-4.63 (m, 2H), 3.42-3.51 (m, 2H), 3.06-3.19 (m, 2H), 2.54-2.70 (m, 2H), 1.86-1.96 (m, 2H).

Intermediate 25: 1-{(endo)-8-Azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 3-[(3-bromo-2-nitrophenyl)amino]-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate was synthesized according to General procedure A from 1-bromo-3-fluoro-2-nitrobenzene and tert-butyl (endo)-3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate.

Step 2: tert-butyl 3-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate was synthesized according to General procedure B from tert-butyl 3-[(3-bromo-2-nitrophenyl)amino]-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate. LCMS [M-isobutene+H]*366.

Step 3: 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 3-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate. LCMS [M+H]⁺ 322. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.42 (s, 1H), 8.71 (br. s., 2H), 7.22 (dd, J=8.1, 0.8 Hz, 1H), 7.11 (d, J=8.1 Hz, 1H), 7.01 (t, J=8.1 Hz, 1H), 4.63-4.77 (m, 1H), 4.06-4.15 (m, 2H), 2.42-2.47 (m, 1H), 2.37-2.42 (m, 1H), 2.13-2.22 (m, 2H), 2.09 (br. s, 4H).

Intermediate 26: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: A mixture of (cis)-4-aminocyclohexanecarboxylic acid (1.5 equiv.), N,N-diisopropylethylamine (3.2 equiv.), and 1-bromo-3-fluoro-2-nitro-benzene (1.0 equiv.) was stirred in MeOH at 120° C. for 6 days. The mixture was poured into HCl (2 M) and extracted with DCM×3. The combined organics were dried and concentrated. The crude material was then suspended in MeOH, after which H₂SO₄ (conc., 2.2 equiv.) was added carefully. The mixture was stirred at reflux for 20 h and was then poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried, concentrated, and purified by silica gel chromatography which afforded methyl (cis)-4-(3-bromo-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 357.

Step 2: methyl (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate was synthesized according to General procedure B from methyl (cis)-4-(3-bromo-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 353. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.89 (br. s., 1H), 7.17 (dd, J=8.2, 0.6 Hz, 1H), 7.12-7.15 (m, 1H), 6.95 (t, J=8.1 Hz, 1H), 4.39 (tt, J=12.6, 4.1 Hz, 1H), 3.79 (s, 3H), 2.74-2.80 (m, 1H), 2.25-2.45 (m, 4H), 1.66-1.82 (m, 4H).

Step 3: (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid was synthesized according to General procedure J from methyl (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate. LCMS [M+H]⁺ 339. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 12.34 (br. s., 1H), 11.28 (s, 1H), 7.16 (d, J=7.9 Hz, 1H), 7.10 (d, J=7.9 Hz, 1H), 6.95 (t, J=7.9 Hz, 1H), 4.13-4.25 (m, 1H), 2.67 (br. s., 1H), 2.09-2.32 (m, 4H), 1.55-1.70 (m, 4H).

Intermediate 27: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: A mixture of cis-4-aminocyclohexanecarboxylic acid (1.5 equiv.), N,N-diisopropylethylamine (3.2 equiv.), and 1-chloro-3-fluoro-2-nitro-benzene (1.0 equiv.) was stirred in MeOH at 120° C. for 6 days. The mixture was poured into HCl (2 M) and extracted with DCM×3. The combined organics were dried and concentrated. The crude material was suspended in MeOH, then H₂SO₄ (conc., 2.2 equiv.) was added carefully. The mixture was stirred at reflux for 20 h and was then poured into NaHCO₃ and extracted with DCM×3. The combined organics were dried, concentrated, and purified by silica gel chromatography which afforded methyl (cis)-4-(3-chloro-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 313.

Step 2: methyl (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate was synthesized according to General procedure B from methyl (cis)-4-(3-chloro-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 309. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.27 (br. s., 1H), 7.08-7.13 (m, 1H), 6.97-7.06 (m, 2H), 4.33-4.46 (m, 1H), 3.79 (s, 3H), 2.78 (br. s., 1H), 2.23-2.44 (m, 4H), 1.66-1.82 (m, 4H).

Step 3: (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid was synthesized according to General procedure J from methyl (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate. LCMS [M+H]⁺ 295. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 12.35 (br. s., 1H), 11.39 (s, 1H), 7.05-7.08 (m, 1H), 6.98-7.05 (m, 2H), 4.20 (tt, J=12.4, 4.0 Hz, 1H), 2.63-2.70 (m, 1H), 2.11-2.32 (m, 4H), 1.55-1.70 (m, 4H).

Intermediate 28: 1-(Azepan-4-yl)-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-bromo-2-nitro-anilino)azepane-1-carboxylate was synthesized according to General procedure A from racemic tert-butyl 4-aminoazepane-1-carboxylate and 1-bromo-3-fluoro-2-nitro-benzene. LCMS [M-isobutene+H]⁺358.

Step 2: tert-butyl 4-(4-bromo-2-oxo-3H-benzimidazol-1-yl)azepane-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-bromo-2-nitro-anilino)azepane-1-carboxylate. LCMS [M+H]⁺ 410.

Step 3: 1-(azepan-4-yl)-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-oxo-3H-benzimidazol-1-yl)azepane-1-carboxylate. LCMS [M+H]⁺ 310.

Intermediate 29: 1-{(endo)-8-Azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 3-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate was synthesized according to General procedure E from tert-butyl 3-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate and [6-(hydroxymethyl)-3-pyridyl]boronic acid. LCMS [M+H]⁺ 451.

Step 2: 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 3-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-(endo)-8-azabicyclo[3.2.1]octane-8-carboxylate. LCMS [M+H]⁺ 351. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.22 (s, 1H), 8.65-8.81 (m, 3H), 8.10 (d, J=7.9 Hz, 1H), 7.68 (d, J=7.6 Hz, 1H), 7.07-7.24 (m, 3H), 4.73-4.83 (m, 1H), 4.71 (br. s., 2H), 4.08-4.17 (m, 2H), 2.38-2.49 (m, 2H), 2.19-2.29 (m, 2H), 2.11 (br. s., 4H).

Intermediate 30: 4-[6-(Hydroxymethyl)pyridin-3-yl]-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-[4-[6-(hydroxymethyl)-3-pyridyl]-2-oxo-3H-benzimidazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure E from tert-butyl 4-(4-bromo-2-oxo-3H-benzimidazol-1-yl)piperidine-1-carboxylate and [6-(hydroxymethyl)-3-pyridyl]boronic acid. LCMS [M-isobutene+H]⁺325.

Step 2: 4-[6-(hydroxymethyl)pyridin-3-yl]-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxylate. LCMS [M+H]⁺ 325. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.19 (s, 1H), 8.63-8.71 (m, 2H), 8.37-8.48 (m, 1H), 8.10 (dd, J=8.1, 2.1 Hz, 1H), 7.67 (d, J=8.1 Hz, 1H), 7.39 (d, J=7.9 Hz, 1H), 7.19 (t, J=7.9 Hz, 1H), 7.11 (dd, J=7.9, 0.9 Hz, 1H), 4.70 (s, 2H), 4.58 (m, 2H), 3.42-3.51 (m, 2H), 3.06-3.19 (m, 2H), 2.61-2.67 (m, 1H), 2.55-2.61 (m, 1H), 1.87-1.94 (m, 2H).

Intermediate 31: 4-bromo-1-(3-hydroxypiperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid

Step 1: tert-butyl 4-(3-bromo-2-nitro-anilino)-3-hydroxy-piperidine-1-carboxylate was synthesized according to General procedure A from tert-butyl 4-amino-3-hydroxy-piperidine-1-carboxylate (produced as described in WO 2011/103091 A1) and 1-bromo-3-fluoro-2-nitrobenzene. LCMS [M+H]⁺ 362.

Step 2: tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-3-hydroxypiperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(3-bromo-2-nitro-anilino)-3-hydroxy-piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺356. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.70 (br. s., 1H), 7.19 (d, J=8.2 Hz, 1H), 7.02-7.06 (m, 1H), 6.93-6.98 (m, 1H), 4.33-4.52 (m, 2H), 4.07-4.17 (m, 1H), 2.83 (br. s., 1H), 2.69 (br. s., 1H), 2.32 (m, 1H), 1.89 (m, 1H), 1.48-1.51 (m, 9H).

Step 3: 4-bromo-1-(3-hydroxypiperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-3-hydroxypiperidine-1-carboxylate.

LCMS [M+H]⁺ 312. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.33 (s, 1H), 8.89 (br. s., 1H), 8.71 (br. s., 1H), 7.26 (br. d, J=8.1 Hz, 1H), 7.19 (dd, J=8.1, 0.9 Hz, 1H), 6.99 (t, J=8.1 Hz, 1H), 5.65 (br. s, 1H), 4.41-4.52 (m, 1H), 4.20-4.31 (m, 1H), 3.34-3.45 (m, 2H), 3.02-3.15 (m, 1H), 2.75-2.87 (m, 1H), 2.53-2.63 (m, 1H), 1.88-1.98 (m, 1H).

Intermediate 32: 4-Bromo-1-(2-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate

Step 1: tert-butyl 4-((3-bromo-2-nitrophenyl)amino)-2-methylpiperidine-1-carboxylate was synthesized according to General procedure A from 1-bromo-3-fluoro-2-nitrobenzene and tert-butyl 4-amino-2-methylpiperidine-1-carboxylate.

Step 2: tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-2-methylpiperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-((3-bromo-2-nitrophenyl)amino)-2-methylpiperidine-1-carboxylate. LCMS [M+H]⁺ 410.

Step 3: 4-bromo-1-(2-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-2-methylpiperidine-1-carboxylate.

LCMS [M+H]⁺ 310.

Intermediate 33: 4-Bromo-1-(3-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate

Step 1: tert-butyl 4-((3-bromo-2-nitrophenyl)amino)-3-methylpiperidine-1-carboxylate was synthesized according to General procedure A from 1-bromo-3-fluoro-2-nitrobenzene and tert-butyl 4-amino-3-methylpiperidine-1-carboxylate.

Step 2: tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-3-methylpiperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-((3-bromo-2-nitrophenyl)amino)-3-methylpiperidine-1-carboxylate. LCMS [M+H]⁺ 410.

Step 3: 4-bromo-1-(3-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-3-methylpiperidine-1-carboxylate.

LCMS [M+H]⁺ 310.

Intermediate 34: Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: methyl 4-(3-methoxy-2-nitro-anilino)cyclohexanecarboxylate was synthesized according to General procedure A from 1-fluoro-3-methoxy-2-nitrobenzene and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 309.

Step 2: methyl cis-4-[4-methoxy-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate was synthesized according to General procedure F from methyl 4-(3-methoxy-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 305.

Step 3: the title compound was synthesized according to General procedure J from methyl cis-4-[4-methoxy-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate. LCMS [M+H]⁺ 291.

Intermediate 35: Cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate

The title compound was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 297.

Intermediate 36: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: methyl cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate was synthesized according to General procedure B from cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate. LCMS [M+H]⁺ 293.

Step 2: the title compound was synthesized according to General procedure J from methyl cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylate. LCMS [M+H]⁺ 279. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 12.35 (br. s., 1H), 11.41 (s, 1H), 6.92-7.02 (m, 2H), 6.84-6.92 (m, 1H), 4.15-4.25 (m, 1H), 2.64-2.70 (m, 1H), 2.19-2.31 (m, 2H), 2.11-2.19 (m, 2H), 1.55-1.70 (m, 4H).

Intermediate 37: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: methyl cis-4-(5-fluoro-2-nitro-anilino)cyclohexanecarboxylate was synthesized according to General procedure A from 2,4-difluoro-1-nitrobenzene and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 297.

Step 2: methyl cis-4-(6-fluoro-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate was synthesized according to General procedure B from methyl cis-4-(5-fluoro-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 293. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 9.61 (br. s., 1H), 6.94-7.04 (m, 2H), 6.78 (t, J=9.0 Hz, 1H), 4.34-4.45 (m, 1H), 3.81 (s, 3H), 2.79 (br. s., 1H), 2.26-2.43 (m, 4H), 1.66-1.83 (m, 4H).

Step 3: the title compound was synthesized according to General procedure J from methyl cis-4-(6-fluoro-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate. LCMS [M+H]⁺ 279.

Intermediate 38: Cis-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxylic acid

Step 1: 1-fluoro-3-(2-methoxyethoxy)-2-nitro-benzene was synthesized according to General procedure K from 1,3-difluoro-2-nitrobenzene and 2-methoxyethanol. LCMS [M+H]⁺ 216. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.35-7.44 (m, 1H), 6.81-6.91 (m, 2H), 4.25 (t, J=4.6 Hz, 2H), 3.75 (t, J=4.6 Hz, 2H), 3.43 (s, 3H).

Step 2: methyl 4-[3-(2-methoxyethoxy)-2-nitro-anilino]cyclohexanecarboxylate was synthesized according to General procedure A from 1-fluoro-3-(2-methoxyethoxy)-2-nitro-benzene and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 353.

Step 3: methyl cis-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxylate was synthesized according to General procedure B from methyl 4-[3-(2-methoxyethoxy)-2-nitro-anilino]cyclohexanecarboxylate. LCMS [M+H]⁺ 349.

Step 4: the title compound was synthesized according to General procedure J from methyl cis-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxylate. LCMS [M+H]⁺ 335.

Intermediate 39: Cis-4-amino-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide hydrochloride

Step 1: tert-butyl N-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]carbamate was synthesized according to General procedure H from 4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid and 3-methoxy-4-methyl-aniline.

LCMS [M-isobutene+H]⁺307. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 9.66 (s, 1H), 7.33 (s, 1H), 7.04-7.09 (m, 1H), 6.98-7.03 (m, 1H), 6.74-6.81 (m, 1H), 3.74 (s, 3H), 3.46-3.54 (m, 1H), 2.31-2.40 (m, 1H), 2.08 (s, 3H), 1.83 (d, J=10.4 Hz, 2H), 1.70 (br. s., 2H), 1.47-1.57 (m, 4H), 1.39 (s, 9H).

Step 2: a mixture of tert-butyl N-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]carbamate (1.0 equiv.) and HCl (4M in dioxane, 2 equiv.) was stirred in DCM for 16 h. The resulting precipitate was collected by filtration, washed with DCM and dried in vacuo. LCMS [M+H]⁺ 263.

Intermediate 40: Cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and cis-4-amino-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide hydrochloride. LCMS [M+H]⁺ 402.

Intermediate 41: Cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylic acid

Step 1: methyl 4-[(2-nitro-3-pyridyl)amino]cyclohexanecarboxylate was synthesized according to General procedure A from 3-fluoro-2-nitro-pyridine and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 280.

Step 2: methyl cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylate was synthesized according to General procedure B from methyl 4-[(2-nitro-3-pyridyl)amino]cyclohexanecarboxylate. LCMS [M+H]⁺ 276.

Step 3: the title compound was synthesized according to General procedure J from methyl cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylate.

LCMS [M+H]⁺ 262.

Intermediate 42: 2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid

Step 1: a mixture of 3-fluoro-2-nitro-benzoic acid, benzyl bromide, and K₂CO₃ was stirred in DMF at 20° C. for 16 h. The mixture was then poured into NaHCO₃ (aq.) and extracted with hexane×5. The combined extracts were dried, concentrated, and purified by silica gel chromatography which afforded benzyl 3-fluoro-2-nitro-benzoate. LCMS [M+H₃O]⁺293. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.57 (br. s, 1H), 7.30-7.42 (m, 7H), 7.01 (d, J=8.5 Hz, 1H), 6.93 (d, J=7.9 Hz, 1H), 6.73-6.78 (m, 2H), 5.32 (s, 2H), 3.81 (s, 3H), 3.77 (br. s., 1H), 2.38-2.47 (m, 1H), 2.16 (s, 3H), 1.75-1.99 (m, 8H).

Step 2: benzyl 3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-benzoate was synthesized according to General procedure A from cis-4-amino-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide hydrochloride and benzyl 3-fluoro-2-nitro-benzoate. LCMS [M+H]⁺ 518.

Step 3: benzyl 1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carboxylate was synthesized according to General procedure B from benzyl 3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-benzoate.

LCMS [M+H]⁺ 514.

Step 4: the title compound was synthesized according to General procedure G from benzyl 1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carboxylate.

Intermediate 43: Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid

Step 1: 4-[3-(dibenzylamino)-2-nitro-anilino]cyclohexanecarboxylic acid was synthesized according to general procedure M from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and dibenzylamine. LCMS [M+H]⁺ 460.

Step 2: 2-Trimethylsilylethyl 4-[3-(dibenzylamino)-2-nitro-anilino]cyclohexanecarboxylate was synthesized according to general procedure O from 4-[3-(dibenzylamino)-2-nitro-anilino]cyclohexanecarboxylic acid and 2-trimethylsilylethanol. LCMS [M+H]⁺ 560. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.21-7.31 (m, 11H), 7.08-7.14 (m, 1H), 6.35-6.44 (m, 2H), 4.16-4.25 (m, 6H), 3.49-3.57 (m, 1H), 2.43-2.52 (m, 1H), 1.92-2.02 (m, 2H), 1.62-1.85 (m, 6H), 0.97-1.03 (m, 2H), 0.05-0.08 (m, 9H).

Step 3: 2-trimethylsilylethyl 4-[4-(dibenzylamino)-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate was synthesized according to general procedure B from 2-trimethylsilylethyl 4-[3-(dibenzylamino)-2-nitro-anilino]cyclohexanecarboxylate. LCMS [M+H]⁺ 556.

Step 4: 2-Trimethylsilylethyl 4-(4-amino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate cyclohexanecarboxylate was synthesized according to general procedure G from 2-trimethylsilylethyl 4-[4-(dibenzylamino)-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate. LCMS [M+H]⁺ 376.

Step 5: A mixture of 2-trimethylsilylethyl 4-(4-amino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate cyclohexanecarboxylate (1.0 equiv.), N,N-diisopropylethylamine (2.0 equiv.), and acetyl chloride (1.0 equiv.) was stirred in DCM at 20° C. for 3 h. The mixture was then purified by silica gel chromatography which afforded 2-trimethylsilylethyl 4-(4-acetamido-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate.

LCMS [M+H]⁺ 418. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 9.86-9.99 (m, 1H), 8.18-8.29 (m, 1H), 6.96-7.09 (m, 3H), 4.34-4.44 (m, 1H), 4.24-4.31 (m, 2H), 2.69-2.74 (m, 1H), 2.28-2.45 (m, 4H), 2.27 (s, 3H), 1.63-1.77 (m, 4H), 1.02-1.09 (m, 2H), 0.08 (s, 9H).

Step 6: A mixture of 2-trimethylsilylethyl 4-(4-acetamido-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate (1.0 equiv.) and TBAF (1M in THF, 4 equiv.) was stirred in DMF for 4 h. The mixture was then diluted to 5 times the volume using a mixture of THE and MeOH (1:1), thereafter Ca(OAc)₂ (25 equiv.) and DOWEX 50WX8 (1500 wt %) were added. The resulting mixture was stirred vigorously for 3 h and then filtered and concentrated. The mixture was then purified by silica gel chromatography. LCMS [M+H]⁺ 318.

EXAMPLE COMPOUNDS

Example compounds as described below were prepared in accordance with the general procedures indicated.

Example 1: 4-(5-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl) piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 4-chlorophenyl isocyanate.

LCMS [M+H]⁺ 405.

Example 2: 4-(5-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl) piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 4-iodophenyl isocyanate.

LCMS [M+H]⁺ 497.

Example 3: 4-(5-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3,4-dichlorophenyl isocyanate.

LCMS [M+H]⁺ 439.

Example 4: N-(4-iodophenyl)-4-(4-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 477.

Example 5: N-(4-iodophenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 493.

Example 6: 4-(4-Hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 479.

Example 7: N-(4-chlorophenyl)-4-(4-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chlorophenyl isocyanate. LCMS [M+H]⁺ 385.

Example 8: N-(4-chlorophenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chlorophenyl isocyanate. LCMS [M+H]⁺ 401.

Example 9: N-(3,4-dichlorophenyl)-4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 421. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.88 (br. s., 1H), 7.87 (dd, J=1.6, 0.9 Hz, 1H), 7.45-7.51 (m, 2H), 6.74-6.80 (m, 1H), 6.66 (d, J=7.9 Hz, 1H), 6.44-6.49 (m, 1H), 4.21-4.41 (m, 3H), 2.94 (m, 2H), 2.25 (m, 2H), 1.71 (m, 2H).

Example 10: 4-(5-Cyano-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 2-oxo-1-(4-piperidyl)-1H-benzimidazole-5-carbonitrile;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 488.

Example 11: N-(4-iodophenyl)-4-(5-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 477. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.70 (s, 1H), 7.56 (d, J=8.5 Hz, 2H), 7.35 (d, J=8.8 Hz, 2H), 7.07 (d, J=8.5 Hz, 1H), 6.75-6.81 (m, 2H), 4.22-4.41 (m, 3H), 2.92 (m, 2H), 2.16-2.30 (m, 5H), 1.70 (m, 2H).

Example 12: 4-(4-Fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 481.

Example 13: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 541. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (s, 1H), 8.69 (s, 1H), 7.53-7.59 (m, 2H), 7.33-7.39 (m, 2H), 7.25 (d, J=7.9 Hz, 1H), 7.16 (d, J=7.6 Hz, 1H), 6.95 (t, J=8.1 Hz, 1H), 4.34-4.45 (m, 1H), 4.28 (m, 2H), 2.93 (m, 2H), 2.26 (m, 2H), 1.74 (m, 2H).

Example 14: N-(4-iodophenyl)-4-(5-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 493. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.78 (s, 1H), 8.70 (s, 1H), 7.55-7.59 (m, 2H), 7.34-7.39 (m, 2H), 7.07-7.12 (m, 1H), 6.57 (m, 2H), 4.24-4.40 (m, 3H), 3.71 (s, 3H), 2.88-2.98 (m, 2H), 2.23 (m, 2H), 1.67-1.76 (m, 2H).

Example 15: N-(4-iodophenyl)-4-(5-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 481. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.70 (s, 1H), 7.53-7.60 (m, 2H), 7.32-7.39 (m, 2H), 7.21 (dd, J=8.5, 4.4 Hz, 1H), 6.77-6.86 (m, 2H), 4.33-4.43 (m, 1H), 4.25-4.32 (m, 2H), 2.89-2.98 (m, 2H), 2.19-2.31 (m, 2H), 1.69-1.77 (m, 2H).

Example 16: Methyl 2-(1-{1-[(4-iodophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)acetate

The title compound was synthesized using General procedure D from methyl 2-[2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-4-yl]acetate;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 535. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.98 (br. s., 1H), 8.71 (s, 1H), 7.54-7.60 (m, 2H), 7.34-7.39 (m, 2H), 7.14 (dd, J=7.9, 0.9 Hz, 1H), 6.95 (t, J=7.9 Hz, 1H), 6.83-6.87 (m, 1H), 4.40 (tt, J=12.3, 4.1 Hz, 1H), 4.25-4.33 (m, 2H), 3.76 (s, 2H), 3.62 (s, 3H), 2.89-3.00 (m, 2H), 2.22-2.35 (m, 2H), 1.69-1.78 (m, 2H).

Example 17: 4-(5-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 5-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-iodophenyl isocyanate. LCMS [M+H]⁺ 531.

Example 18: 4-(4-Ethoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-ethoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 507. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.92 (br. s., 1H), 8.71 (br. s., 1H), 7.54-7.60 (m, 2H), 7.34-7.39 (m, 2H), 6.89-6.96 (m, 1H), 6.82-6.87 (m, 1H), 6.66-6.71 (m, 1H), 4.33-4.43 (m, 1H), 4.24-4.33 (m, 2H), 4.08-4.16 (m, 2H), 2.87-3.00 (m, 2H), 2.18-2.35 (m, 2H), 1.67-1.76 (m, 2H), 1.34 (br. t, J=6.5, 6.5 Hz, 3H).

Example 19: N-(4-iodophenyl)-4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methylamino-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 492. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.21 (s, 1H), 8.70 (s, 1H), 7.55-7.59 (m, 2H), 7.34-7.38 (m, 2H), 6.85 (t, J=8.1 Hz, 1H), 6.55 (d, J=8.1 Hz, 1H), 6.27 (d, J=8.1 Hz, 1H), 4.99 (q, J=5.2 Hz, 1H), 4.31-4.38 (m, 1H), 4.27 (m, 2H), 2.88-2.98 (m, 2H), 2.79 (d, J=5.2 Hz, 3H), 2.20-2.32 (m, 2H), 1.66-1.74 (m, 2H).

Example 20: 4-(4-Amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-amino-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 478. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.27 (s, 1H), 8.69 (s, 1H), 7.54-7.59 (m, 2H), 7.32-7.38 (m, 2H), 6.72 (t, J=8.0 Hz, 1H), 6.46 (d, J=8.0 Hz, 1H), 6.30 (dd, J=8.1, 0.8 Hz, 1H), 4.91 (s, 2H), 4.22-4.37 (m, 3H), 2.86-2.97 (m, 2H), 2.18-2.31 (m, 2H), 1.65-1.73 (m, 2H).

Example 21: 4-(4-Dimethylamino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-dimethylamino-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 506. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.77 (s, 1H), 8.71 (s, 1H), 7.54-7.60 (m, 2H), 7.34-7.39 (m, 2H), 6.92 (t, J=7.9 Hz, 1H), 6.84-6.87 (m, 1H), 6.60 (dd, J=7.9, 0.9 Hz, 1H), 4.33-4.42 (m, 1H), 4.25-4.32 (m, 2H), 2.89-2.98 (m, 2H), 2.69 (s, 6H), 2.22-2.35 (m, 2H), 1.68-1.76 (m, 2H).

Example 22: N-(4-iodophenyl)-4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 1-(piperidin-4-yl)-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]*529.

Example 23: N-(4-iodophenyl)-4-[2-oxo-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 1-(piperidin-4-yl)-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 530. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.02 (br. s., 1H), 9.11 (s, 1H), 8.72 (s, 1H), 8.27 (s, 1H), 7.55-7.60 (m, 2H), 7.34-7.40 (m, 3H), 7.32 (dd, J=8.1, 0.9 Hz, 1H), 7.16 (t, J=8.2 Hz, 1H), 4.41-4.53 (m, 1H), 4.26-4.35 (m, 2H), 2.92-3.02 (m, 2H), 2.25-2.38 (m, 2H), 1.73-1.82 (m, 2H).

Example 24: N-(4-iodophenyl)-4-[4-(methylsulfanyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-methylsulfanyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 509. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.06 (br. s., 1H), 8.71 (br. s., 1H), 7.54-7.61 (m, 2H), 7.34-7.40 (m, 2H), 7.12 (dd, J=3.0, 2.4 Hz, 1H), 6.96-7.04 (m, 2H), 4.34-4.46 (m, 1H), 4.24-4.33 (m, 2H), 2.88-3.00 (m, 2H), 2.45 (s, 3H), 2.21-2.36 (m, 2H), 1.68-1.78 (m, 2H).

Example 25: N-(4-iodophenyl)-4-[2-oxo-4-(1H-pyrrol-2-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

Step 1: A mixture of tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate (1.0 equiv.), potassium {1-[(tert-butoxy)carbonyl]-1H-pyrrol-2-yl}trifluoroboranuide (1.5 equiv.), Pd(OAc)₂ (0.10 equiv.), 2-Dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.20 equiv.), and Na₂CO₃ (2.0 equiv.) was stirred in ethanol at reflux for 5 h. The mixture was then concentrated and purified by silica gel chromatography which afforded tert-butyl 4-(4-{1-[(tert-butoxy)carbonyl]-1H-pyrrol-2-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺383.

Step 2: 1-(piperidin-4-yl)-4-(1H-pyrrol-2-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized using General procedure C from tert-butyl 4-(4-{1-[(tert-butoxy)carbonyl]-1H-pyrrol-2-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 283.

Step 3: The title compound was synthesized using General procedure D from 1-(piperidin-4-yl)-4-(1H-pyrrol-2-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 528. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.19 (br. s., 1H), 10.62 (s, 1H), 8.72 (s, 1H), 7.55-7.60 (m, 2H), 7.35-7.40 (m, 2H), 7.21 (dd, J=7.9, 1.1 Hz, 1H), 7.08-7.12 (m, 1H), 7.04 (t, J=7.9 Hz, 1H), 6.88 (td, J=2.7, 1.3 Hz, 1H), 6.64 (td, J=3.0, 1.6 Hz, 1H), 6.16 (dt, J=3.5, 2.4 Hz, 1H), 4.38-4.49 (m, 1H), 4.27-4.35 (m, 2H), 2.91-3.01 (m, 2H), 2.27-2.39 (m, 2H), 1.71-1.80 (m, 2H).

Example 26: N-(4-iodophenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 1-(piperidin-4-yl)-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 540. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.10 (s, 1H), 8.71-8.74 (m, 2H), 8.59 (dd, J=4.9, 1.7 Hz, 1H), 7.94 (ddd, J=7.9, 2.2, 1.6 Hz, 1H), 7.55-7.60 (m, 2H), 7.49 (ddd, J=7.9, 4.9, 0.8 Hz, 1H), 7.35-7.40 (m, 2H), 7.31 (br. d, J=7.9 Hz, 1H), 7.14 (t, J=7.9 Hz, 1H), 7.06 (dd, J=7.9, 1.0 Hz, 1H), 4.41-4.51 (m, 1H), 4.27-4.35 (m, 2H), 2.92-3.02 (m, 2H), 2.27-2.40 (m, 2H), 1.73-1.81 (m, 2H).

Example 27: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 483.

Example 28: N-(3,4-dichlorophenyl)-4-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [6-(hydroxymethyl)-3-pyridyl]boronic acid.

LCMS [M+H]⁺ 512. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.22 (s, 1H), 8.90 (s, 1H), 8.79 (d, J=1.6 Hz, 1H), 8.30 (dd, J=8.2, 1.9 Hz, 1H), 7.89 (t, J=1.3 Hz, 1H), 7.81 (d, J=8.2 Hz, 1H), 7.49 (d, J=1.6 Hz, 2H), 7.36 (d, J=7.9 Hz, 1H), 7.16 (t, J=7.6 Hz, 1H), 7.11 (dd, J=7.9, 0.9 Hz, 1H), 4.78 (s, 2H), 4.47 (ddt, J=16.3, 8.1, 3.9, 3.9 Hz, 1H), 4.31 (m, 2H), 2.99 (m, 2H), 2.26-2.39 (m, 2H), 1.73-1.81 (m, 2H).

Example 29: 4-[4-(3-Aminophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 3-aminophenylboronic acid. LCMS [M+H]⁺ 496. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.71 (br. s., 1H), 8.90 (s, 1H), 7.90 (t, J=1.3 Hz, 1H), 7.50 (d, J=1.6 Hz, 2H), 7.19-7.23 (m, 1H), 7.11 (t, J=7.7 Hz, 1H), 7.06 (t, J=7.9 Hz, 1H), 6.96-6.99 (m, 1H), 6.73 (t, J=1.9 Hz, 1H), 6.65-6.69 (m, 1H), 6.58 (ddd, J=8.0, 2.1, 0.9 Hz, 1H), 5.11 (s, 2H), 4.40-4.50 (m, 1H), 4.28-4.35 (m, 2H), 2.94-3.03 (m, 2H), 2.27-2.40 (m, 2H), 1.73-1.82 (m, 2H).

Example 30: 4-[4-(2-Hydroxyethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-iodophenyl)piperidine-1-carboxamide

Step 1: A mixture of tert-butyl 4-[4-(2-methoxy-2-oxo-ethyl)-2-oxo-3H-benzimidazol-1-yl]piperidine-1-carboxylate (1.0 equiv.) and NaBH₄ (4.0 equiv.) in THE was stirred at 20° C. for 16 h. The mixture was then poured into NaHCO₃ and extracted with DCM×3. The combined organics were concentrated and purified by silica gel chromatography which afforded tert-butyl 4-[4-(2-hydroxyethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 362. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 10.36 (s, 1H), 6.99-7.06 (m, 2H), 6.91 (dd, J=7.0, 1.9 Hz, 1H), 4.45 (tt, J=12.4, 4.0 Hz, 1H), 4.32 (d, J=12.0 Hz, 2H), 3.96 (t, J=5.8 Hz, 2H), 3.00 (t, J=5.8 Hz, 2H), 2.87 (m, 2H), 2.33 (m, 2H), 1.79-1.86 (m, 2H), 1.52 (s, 9H).

Step 2: 4-(2-hydroxyethyl)-1-(4-piperidyl)-1H-benzimidazol-2-one;2,2,2-trifluoroacetic acid was synthesized using General procedure C from tert-butyl 4-[4-(2-hydroxyethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 262.

Step 3: The title compound was synthesized using General procedure D from 4-(2-hydroxyethyl)-1-(4-piperidyl)-1H-benzimidazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 507. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.71 (s, 1H), 7.54-7.60 (m, 2H), 7.34-7.39 (m, 2H), 7.05 (dd, J=7.9, 0.9 Hz, 1H), 6.91 (t, J=7.9 Hz, 1H), 6.83 (br. d, J=7.9 Hz, 1H), 4.34-4.44 (m, 1H), 4.25-4.33 (m, 2H), 3.61 (t, J=6.8 Hz, 2H), 2.89-2.99 (m, 2H), 2.79 (t, J=6.8 Hz, 2H), 2.21-2.35 (m, 2H), 1.68-1.76 (m, 2H).

Example 31: 4-(4-Cyclopropyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

Step 1: tert-butyl 4-(4-cyclopropyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized using General procedure E from tert-butyl 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate and cyclopropylboronic acid.

LCMS [M-isobutene+H]⁺302.

Step 2: 4-cyclopropyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one was synthesized using General procedure C from tert-butyl 4-(4-cyclopropyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 258.

Step 3: The title compound was synthesized using General procedure D from 4-cyclopropyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 4-iodophenyl isocyanate.

LCMS [M+H]⁺ 503. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 8.71 (s, 1H), 7.54-7.59 (m, 2H), 7.34-7.39 (m, 2H), 7.01 (d, J=7.9 Hz, 1H), 6.89 (t, J=7.9 Hz, 1H), 6.50 (d, J=7.9 Hz, 1H), 4.34-4.44 (m, 1H), 4.25-4.33 (m, 2H), 2.90-2.99 (m, 2H), 2.22-2.35 (m, 2H), 1.99-2.07 (m, 1H), 1.69-1.77 (m, 2H), 0.91-0.97 (m, 2H), 0.64-0.70 (m, 2H).

Example 32: N-(3,4-dichlorophenyl)-4-[2-oxo-4-(pyridin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 4-pyridineboronic acid pinacol ester.

LCMS [M+H]⁺ 482.

Example 33: 4-{4-[4-(Aminomethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 4-aminomethylphenylboronic acid;hydrochloride. LCMS [M+H]⁺ 510.

Example 34: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)azepane-1-carboxamide

The title compound was synthesized using General procedure D from 1-(azepan-4-yl)-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 555. ¹H-NMR (400 MHz, DMSO-d₆) ppm 11.29 (s, 1H), 8.40 (s, 1H), 7.57 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.8 Hz, 2H), 7.23 (d, J=8.0 Hz, 1H), 7.16 (d, J=8.0 Hz, 1H), 6.94 (t, J=8.0 Hz, 1H), 4.31 (br. s., 1H), 3.65-3.81 (m, 2H), 3.41-3.51 (m, 2H), 2.25-2.40 (m, 2H), 1.87-2.00 (m, 2H), 1.66-1.84 (m, 2H).

Example 35: 4-(1-{1-[(3,4-Dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoic acid

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 4-carboxyphenylboronic acid. LCMS [M+H]⁺ 525.

Example 36: N-(3,4-dichlorophenyl)-4-(4-{4-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (4-[2-(dimethylamino)ethoxy]phenyl)boronic acid. LCMS [M+H]⁺ 568.

Example 37: N-(3,4-dichlorophenyl)-4-[2-oxo-4-(pyrimidin-5-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (pyrimidin-5-yl)boronic acid.

LCMS [M+H]⁺ 483.

Example 38: 4-{4-[3,5-Bis(trifluoromethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [3,5-bis(trifluoromethyl)phenyl]boronic acid.

LCMS [M+H]⁺ 617.

Example 39: 4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized using General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (6-aminopyridin-3-yl)boronic acid.

LCMS [M+H]⁺ 497.

Example 40: N-(3,4-dichlorophenyl)-4-{2-oxo-4-[4-(2,2,2-trifluoroacetyl)phenyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [4-(2,2,2-trifluoroacetyl)phenyl]boronic acid.

LCMS [M+H]⁺ 577.

Example 41: 4-[4-(4-Bromo-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-(4-bromo-1H-pyrazol-1-yl)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate.

LCMS [M+H]⁺ 607. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.82 (br. s., 1H), 8.72 (s, 1H), 8.66 (s, 1H), 7.89 (s, 1H), 7.55-7.60 (m, 2H), 7.35-7.39 (m, 2H), 7.26-7.32 (m, 2H), 7.09-7.15 (m, 1H), 4.41-4.52 (m, 1H), 4.26-4.35 (m, 2H), 2.91-3.01 (m, 2H), 2.25-2.38 (m, 2H), 1.72-1.81 (m, 2H).

Example 42: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-ethylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-ethylphenyl isocyanate. LCMS [M+H]⁺ 443. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.51 (s, 1H), 7.36-7.41 (m, 2H), 7.25 (d, J=8.1 Hz, 1H), 7.17 (d, J=8.1 Hz, 1H), 7.08 (d, J=8.8 Hz, 2H), 6.96 (t, J=8.1 Hz, 1H), 4.40 (ddt, J=12.3, 8.2, 4.0, 4.0 Hz, 1H), 4.30 (m, 2H), 2.88-2.97 (m, 2H), 2.53-2.58 (m, 2H), 2.20-2.33 (m, 2H), 1.70-1.78 (m, 2H), 1.16 (t, J=7.6 Hz, 3H).

Example 43: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-methylphenyl isocyanate. LCMS [M+H]⁺ 429. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.49 (s, 1H), 7.35-7.39 (m, 2H), 7.25 (d, J=8.1 Hz, 1H), 7.17 (dd, J=8.1, 0.6 Hz, 1H), 7.05 (dd, J=8.8, 0.6 Hz, 2H), 6.96 (t, J=8.1 Hz, 1H), 4.34-4.45 (m, 1H), 4.26-4.33 (m, 2H), 2.87-2.97 (m, 2H), 2.20-2.33 (m, 5H), 1.70-1.78 (m, 2H).

Example 44: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-methoxyphenyl isocyanate. LCMS [M+H]⁺ 445. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.43 (s, 1H), 7.35-7.41 (m, 2H), 7.23-7.27 (m, 1H), 7.17 (dd, J=8.2, 0.9 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 6.81-6.87 (m, 2H), 4.34-4.44 (m, 1H), 4.24-4.33 (m, 2H), 3.72 (s, 3H), 2.87-2.97 (m, 2H), 2.20-2.32 (m, 2H), 1.69-1.79 (m, 2H).

Example 45: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 3,4-dimethoxyphenyl isocyanate. LCMS [M+H]⁺ 475. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.43 (br. s., 1H), 7.23-7.29 (m, 1H), 7.14-7.22 (m, 2H), 6.99-7.04 (m, 1H), 6.93-6.99 (m, 1H), 6.82-6.86 (m, 1H), 4.35-4.45 (m, 1H), 4.25-4.33 (m, 2H), 3.72 (s, 3H), 3.71 (br. s., 3H), 2.86-2.98 (m, 2H), 2.19-2.36 (m, 2H), 1.75 (m, 2H).

Example 46: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 3-chloro-4-methoxyphenyl isocyanate. LCMS [M+H]⁺ 479. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.58 (s, 1H), 7.65 (d, J=2.5 Hz, 1H), 7.38 (dd, J=9.0, 2.5 Hz, 1H), 7.27 (br. d, J=8.1 Hz, 1H), 7.17 (dd, J=8.1, 0.6 Hz, 1H), 7.06 (d, J=9.0 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 4.35-4.45 (m, 1H), 4.28 (m, 2H), 3.81 (s, 3H), 2.89-2.98 (m, 2H), 2.20-2.32 (m, 2H), 1.71-1.79 (m, 2H).

Example 47: N-(2H-1,3-benzodioxol-5-yl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 5-isocyanato-2H-1,3-benzodioxole. LCMS [M+H]⁺ 459. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.48 (s, 1H), 7.26 (dd, J=8.1, 0.9 Hz, 1H), 7.18 (d, J=2.1 Hz, 1H), 7.17 (dd, J=8.1, 0.9 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 6.87 (dd, J=8.3, 2.1 Hz, 1H), 6.80 (d, J=8.3 Hz, 1H), 5.96 (s, 2H), 4.34-4.44 (m, 1H), 4.23-4.32 (m, 2H), 2.86-2.97 (m, 2H), 2.19-2.32 (m, 2H), 1.69-1.79 (m, 2H).

Example 48: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-bromo-3-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-bromo-3-methylphenyl isocyanate. LCMS [M+H]⁺ 507. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.32 (s, 1H), 8.66 (s, 1H), 7.51 (d, J=2.7 Hz, 1H), 7.42 (d, J=8.7 Hz, 1H), 7.31 (dd, J=8.7, 2.7 Hz, 1H), 7.26 (dd, J=8.1, 0.6 Hz, 1H), 7.17 (dd, J=8.1, 0.7 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 4.40 (tt, J=12.2, 3.9 Hz, 1H), 4.25-4.34 (m, 2H), 2.89-2.99 (m, 2H), 2.30 (s, 3H), 2.20-2.30 (m, 2H), 1.71-1.79 (m, 2H).

Example 49: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-bromo-3-chlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-bromo-3-chloroaniline. LCMS [M+H]⁺ 527.

Example 50: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodo-3-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 4-iodo-3-methylaniline. LCMS [M+H]⁺ 555. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.64 (s, 1H), 7.65 (d, J=8.8 Hz, 1H), 7.51 (d, J=2.5 Hz, 1H), 7.26 (br. d, J=8.1 Hz, 1H), 7.13-7.19 (m, 3H), 6.96 (t, J=8.1 Hz, 1H), 4.35-4.45 (m, 1H), 4.24-4.33 (m, 2H), 2.89-2.99 (m, 2H), 2.32 (s, 3H), 2.20-2.31 (m, 2H), 1.70-1.79 (m, 2H).

Example 51: 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)-3-trans-hydroxypiperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(3-hydroxypiperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 501. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.25 (br. s., 1H), 8.94 (s, 1H), 7.89 (dd, J=1.6, 0.9 Hz, 1H), 7.49-7.50 (m, 2H), 7.22 (br. d, J=8.1 Hz, 1H), 7.15 (br. d, J=8.1 Hz, 1H), 6.94 (t, J=8.1 Hz, 1H), 5.32 (d, J=5.1 Hz, 1H), 4.30-4.38 (m, 1H), 4.05-4.25 (m, 3H), 2.90-3.00 (m, 1H), 2.63-2.71 (m, 1H), 2.28-2.36 (m, 1H), 1.74-1.82 (m, 1H).

Example 52: 4-(5-Hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

Step 1: tert-butyl 4-(4-hydroxy-2-nitro-anilino)piperidine-1-carboxylate was synthesized according to General procedure A from tert-butyl 4-amino-piperidine-1-carboxylate and 4-fluoro-3-nitrophenol. LCMS [M-isobutene+H]⁺282.

Step 2: tert-butyl 4-(4-hydroxy-2-nitro-anilino)piperidine-1-carboxylate (1.0 equiv.) was dissolved in THF, then NaH (60 wt % in mineral oil, 1.1 equiv.) was added and the resulting mixture was stirred at 20° C. for 2 min under a stream of N₂. Thereafter acetic anhydride (1.2 equiv.) was added and the resulting mixture was stirred at 20° C. in a sealed tube. After complete reaction, the mixture was poured into NaHCO₃ (aq.) and extracted with DCM×3. The combined organics were concentrated and purified by silica gel chromatography which afforded tert-butyl 4-(4-acetoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺324.

Step 3: tert-butyl 4-[5-(acetyloxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-(4-acetoxy-2-nitro-anilino)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺320.

Step 4: A mixture of tert-butyl 4-[5-(acetyloxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate and NaHCO₃ (aq.) was stirred in MeOH at 20° C. for 16 h.

After complete reaction, the mixture was poured into NaHCO₃ (aq.) and extracted with DCM×3. The combined organics were concentrated and purified by silica gel chromatography which afforded N-tert-butyl-4-(5-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide. LCMS [M-isobutene+H]⁺278.

Step 5: 5-hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one; 2,2,2-trifluoroacetic acid was synthesized according to General procedure C from N-tert-butyl-4-(5-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide.

LCMS [M+H]⁺ 234.

Step 6: The title compound was synthesized according to General procedure D from 5-hydroxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodophenyl isocyanate. LCMS [M+H]⁺ 479. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 10.60 (s, 1H), 9.00 (s, 1H), 8.69 (s, 1H), 7.54-7.59 (m, 2H), 7.34-7.38 (m, 2H), 6.97 (d, J=8.5 Hz, 1H), 6.43 (d, J=2.5 Hz, 1H), 6.39 (dd, J=8.5, 2.5 Hz, 1H), 4.21-4.37 (m, 3H), 2.86-2.97 (m, 2H), 2.14-2.28 (m, 2H), 1.64-1.74 (m, 2H).

Example 53: N-(3,4-dichlorophenyl)-4-{2-oxo-4-[2-(trifluoromethyl)pyridin-4-yl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine. LCMS [M+H]⁺ 550.

Example 54: 4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-amine. LCMS [M+H]⁺ 497.

Example 55: N-(3,4-dichlorophenyl)-4-[4-(2-ethoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (2-ethoxy-3-pyridyl)boronic acid.

LCMS [M+H]⁺ 526.

Example 56: N-(3,4-dichlorophenyl)-4-[4-(6-methoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (6-methoxy-3-pyridyl)boronic acid.

LCMS [M+H]⁺ 512.

Example 57: 4-{4-[3-(Carbamoylmethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide.

LCMS [M+H]⁺ 538.

Example 58: 3-(1-{1-[(3,4-Dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoic acid

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 3-carboxyphenylboronic acid.

LCMS [M+H]⁺ 525.

Example 59: Methyl 3-(1-{1-[(3,4-dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoate

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 3-(methoxycarbonyl)phenylboronic acid.

LCMS [M+H]⁺ 539.

Example 60: N-(3,4-dichlorophenyl)-4-(4-{3-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and N,N-dimethyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanamine. LCMS [M+H]⁺ 568.

Example 61: N-(3,4-dichlorophenyl)-4-{4-[3-(morpholine-4-carbonyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [3-(morpholine-4-carbonyl)phenyl]boronic acid.

LCMS [M+H]⁺ 594.

Example 62: N-(3,4-dichlorophenyl)-4-(4-{3-[(2-methoxyethyl)carbamoyl]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [3-(2-methoxyethylcarbamoyl)phenyl]boronic acid. LCMS [M+H]⁺ 582.

Example 63: N-(3,4-dichlorophenyl)-4-[2-oxo-4-(4-sulfamoylphenyl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and (4-sulfamoylphenyl)boronic acid.

LCMS [M+H]⁺ 560.

Example 64: N-(3,4-dichlorophenyl)-4-[4-(3-fluorophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 3-fluorophenylboronic acid. LCMS [M+H]⁺ 499.

Example 65: 4-{4-[3-(Aminomethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [3-(aminomethyl)phenyl]boronic acid;hydrochloride. LCMS [M+H]⁺ 510.

Example 66: 4-[4-(2-Aminophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and 2-aminophenylboronic acid.

LCMS [M+H]⁺ 496.

Example 67: N-(3,4-dichlorophenyl)-4-(4-{2-[(dimethylamino)methyl]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide and [2-[(dimethylamino)methyl]phenyl]boronic acid. LCMS [M+H]⁺ 538.

Example 68: 4-(4-Bromo-2-sulfanylidene-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

Step 1: To a stirred suspension of tert-butyl 4-[(2-amino-3-bromophenyl)amino]piperidine-1-carboxylate (1.0 equiv.) and K₂CO₃ (2.0 equiv.) in an ethanol-water (1:2 v/v) mixture was added CS₂ (2.0 equiv.). The reaction mixture was stirred at 80° C. for 16 h. At this time another 2 equivalents of CS₂ was added and the resulting mixture was stirred another 24 h at 100° C. The reaction mixture was then cooled to room temperature and pour into NaHCO₃ (sat.) and extracted with DCM×3. The combined organics were dried (MgSO₄) and purified by silica gel chromatography which afforded tert-butyl 4-(4-bromo-2-sulfanylidene-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺358.

Step 2: 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazole-2-thione;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-bromo-2-sulfanylidene-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate.

LCMS [M+H]⁺ 312.

Step 3: The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazole-2-thione;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 499. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 13.26 (br. s., 1H), 8.91 (s, 1H), 7.90 (t, J=1.3 Hz, 1H), 7.57 (d, J=8.1 Hz, 1H), 7.50 (s, 1H), 7.50 (s, 1H), 7.39 (d, J=8.2 Hz, 1H), 7.11 (t, J=8.1 Hz, 1H), 5.33 (br. s., 1H), 4.30-4.41 (m, 2H), 2.93-3.06 (m, 2H), 2.25-2.45 (m, 2H), 1.73-1.83 (m, 2H).

Example 69: N-(3,4-dichlorophenyl)-4-(7-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 7-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 423. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.24 (br. s., 1H), 8.90 (s, 1H), 7.87 (dd, J=1.9, 0.9 Hz, 1H), 7.46-7.52 (m, 2H), 6.97-7.03 (m, 1H), 6.84-6.92 (m, 2H), 4.51-4.62 (m, 1H), 4.23-4.31 (m, 2H), 2.92-3.02 (m, 2H), 2.05-2.20 (m, 2H), 1.73-1.82 (m, 2H).

Example 70: 4-(7-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 7-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 439. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.09-11.38 (m, 1H), 8.89 (s, 1H), 7.86-7.90 (m, 1H), 7.48-7.51 (m, 2H), 7.03 (dd, J=7.6, 2.0 Hz, 1H), 6.99 (t, J=7.6 Hz, 1H), 6.95 (dd, J=7.6, 2.0 Hz, 1H), 5.11 (br. s., 1H), 4.23-4.34 (m, 2H), 2.45-2.97 (overlapping m, 2H), 2.56 (br. s., 2H), 1.74-1.86 (m, 2H).

Example 71: 4-(7-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 7-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 483. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.19 (br. s., 1H), 8.89 (s, 1H), 7.87-7.89 (m, 1H), 7.48-7.51 (m, 2H), 7.19 (dd, J=8.0, 1.3 Hz, 1H), 6.99 (dd, J=8.0, 1.3 Hz, 1H), 6.92 (t, J=8.0 Hz, 1H), 5.28 (br. s., 1H), 4.24-4.34 (m, 2H), 2.82-2.94 (m, 2H), 2.53-2.58 (m, 2H), 1.75-1.85 (m, 2H).

Example 72: 3-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure D from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3,4-dichlorophenyl isocyanate.

LCMS [M+H]⁺ 509.

Example 73: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 6-aminoindol. LCMS [M+H]⁺ 454.

Example 74: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methyl-3-(trifluoromethyl)phenyl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-isocyanato-1-methyl-2-(trifluoromethyl)benzene. LCMS [M+H]⁺ 497. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.32 (br. s., 1H), 8.82 (s, 1H), 7.90 (d, J=2.2 Hz, 1H), 7.68 (dd, J=8.4, 2.2 Hz, 1H), 7.31 (d, J=8.4 Hz, 1H), 7.27 (br. d, J=8.1 Hz, 1H), 7.17 (dd, J=8.1, 0.6 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 4.36-4.46 (m, 1H), 4.27-4.35 (m, 2H), 2.90-3.01 (m, 2H), 2.37 (br. d, J=1.6 Hz, 3H), 2.21-2.33 (m, 2H), 1.72-1.80 (m, 2H).

Example 75: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 459. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.32 (br. s., 1H), 8.50 (s, 1H), 7.25 (dd, J=8.1, 0.8 Hz, 1H), 7.18 (d, J=1.9 Hz, 1H), 7.16 (dd, J=8.2, 0.9 Hz, 1H), 7.00 (dd, J=8.2, 1.9 Hz, 1H), 6.97 (s, 1H), 6.94 (d, J=8.2 Hz, 1H), 4.39 (tt, J=12.2, 4.0 Hz, 1H), 4.24-4.33 (m, 2H), 3.74 (s, 3H), 2.85-2.97 (m, 2H), 2.20-2.33 (m, 2H), 2.07 (s, 3H), 1.70-1.79 (m, 2H).

Example 76: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-fluoro-3-methoxyaniline. LCMS [M+H]⁺ 463.

Example 77: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-methoxaniline. LCMS [M+H]⁺ 479. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.32 (br. s., 1H), 8.71 (s, 1H), 7.42 (d, J=2.2 Hz, 1H), 7.25 (s, 1H), 7.13-7.19 (m, 2H), 6.96 (t, J=8.1 Hz, 1H), 4.36-4.46 (m, 1H), 4.26-4.34 (m, 2H), 3.81 (s, 3H), 2.87-3.01 (m, 2H), 2.20-2.36 (m, 2H), 1.71-1.81 (m, 2H).

Example 78: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-fluorophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-fluoroaniline. LCMS [M+H]⁺ 467.

Example 79: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-fluoro-3-methylaniline. LCMS [M+H]⁺ 447. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.55 (s, 1H), 7.39 (dd, J=7.3, 2.2 Hz, 1H), 7.27-7.32 (m, 1H), 7.26 (dd, J=8.1, 0.8 Hz, 1H), 7.17 (dd, J=8.1, 0.8 Hz, 1H), 7.01 (t, J=9.2 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 4.35-4.45 (m, 1H), 4.24-4.33 (m, 2H), 2.87-2.98 (m, 2H), 2.21-2.32 (m, 2H), 2.20 (s, 3H), 1.70-1.79 (m, 2H).

Example 80: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-chloro-4-(trifluoromethoxy)phenyl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-chloro-4-(trifluoromethoxy)aniline.

LCMS [M+H]⁺ 533. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.31 (br. s., 1H), 8.95 (s, 1H), 7.90 (d, J=2.5 Hz, 1H), 7.55 (dd, J=9.0, 2.5 Hz, 1H), 7.43-7.48 (m, 1H), 7.27 (d, J=8.2 Hz, 1H), 7.17 (d, J=8.2 Hz, 1H), 6.96 (t, J=8.2 Hz, 1H), 4.37-4.47 (m, 1H), 4.26-4.33 (m, 2H), 2.92-3.03 (m, 2H), 2.22-2.32 (m, 2H), 1.73-1.80 (m, 2H).

Example 81: 4-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodo-3-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-[6-(hydroxymethyl)pyridin-3-yl]-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodo-3-methylaniline.

LCMS [M+H]⁺ 584.

Example 82: 4-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-[6-(hydroxymethyl)pyridin-3-yl]-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline.

LCMS [M+H]⁺ 488.

Example 83: N-(4-Chloro-3-methoxyphenyl)-4-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-[6-(hydroxymethyl)pyridin-3-yl]-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-methoxyanilin.

LCMS [M+H]⁺ 508.

Example 84: 3-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodo-3-methylphenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodo-3-methylaniline. LCMS [M+H]⁺ 581.

Example 85: 3-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 485.

Example 86: 3-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-fluorophenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-bromo-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-fluoroaniline. LCMS [M+H]⁺ 493.

Example 87: 4-{4-[4-(Ethylcarbamoyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure H from 1-(1-(1-((4-iodophenyl)carbamoyl)piperidin-4-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)-1H-pyrazole-4-carboxylic acid and ethylamine. LCMS [M+H]⁺ 600.

Example 88: 4-{4-[4-(Diethylcarbamoyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure H from 1-(1-(1-((4-iodophenyl)carbamoyl)piperidin-4-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)-1H-pyrazole-4-carboxylic acid and diethylamine. LCMS [M+H]⁺ 628.

Example 89: 4-(4-(4-((2-(Dimethylamino)ethyl)carbamoyl)-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide 2,2,2-trifluoroacetate

The title compound was synthesized according to General procedure H from 1-(1-(1-((4-iodophenyl)carbamoyl)piperidin-4-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)-1H-pyrazole-4-carboxylic acid and N,N-dimethylethylenediamine. LCMS [M+H]⁺ 643.

Example 90: 4-(4-{4-[(2,3-Dihydroxypropyl)carbamoyl]-1H-pyrazol-1-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure H from 1-(1-(1-((4-iodophenyl)carbamoyl)piperidin-4-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-4-yl)-1H-pyrazole-4-carboxylic acid and (±)-amino-1,2-propanediol. LCMS [M+H]⁺ 646.

Example 91: 3-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodo-3-methylphenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-iodo-3-methylaniline. LCMS [M+H]⁺ 610.

Example 92: 3-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 514.

Example 93: N-(4-chloro-3-methoxyphenyl)-3-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-methoxyaniline. LCMS [M+H]⁺ 534.

Example 94: N-(4-chloro-3-fluorophenyl)-3-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-(endo)-8-azabicyclo[3.2.1]octane-8-carboxamide

The title compound was synthesized according to General procedure I from 1-{(endo)-8-azabicyclo[3.2.1]octan-3-yl}-4-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 4-chloro-3-fluoroaniline. LCMS [M+H]⁺ 522.

Example 95: N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide and 3-pyridylboronic acid. LCMS [M+H]⁺ 458.

Example 96: 4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine. LCMS [M+H]⁺ 473.

Example 97: 4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-amine. LCMS [M+H]⁺ 473.

Example 98: N-(3-chloro-4-methoxyphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide and 3-pyridylboronic acid. LCMS [M+H]⁺ 478.

Example 99: 4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine. LCMS [M+H]⁺ 493.

Example 100: 4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-amine. LCMS [M+H]⁺ 493.

Example 101: N-(3-chloro-4-methoxyphenyl)-4-(2-oxo-4-{1H-pyrazolo[3,4-b]pyridin-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide and 1H-pyrazolo[3,4-b]pyridin-5-ylboronic acid. LCMS [M+H]⁺ 518.

Example 102: N-(4-chloro-3-methoxyphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide and 3-pyridylboronic acid. LCMS [M+H]⁺ 478.

Example 103: 4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine. LCMS [M+H]⁺ 493.

Example 104: 4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-amine. LCMS [M+H]⁺ 493.

Example 105: N-(4-chloro-3-methoxyphenyl)-4-[4-(6-methoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure E from 4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide and (6-methoxy-3-pyridyl)boronic acid.

LCMS [M+H]⁺ 508.

Example 106: N-(3-chloro-4-methoxyphenyl)-4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

Step 1: tert-butyl 4-[3-[2-(dimethylamino)ethyl-methyl-amino]-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate and N,N′,N′-trimethylethane-1,2-diamine.

LCMS [M+H]⁺ 422.

Step 2: tert-butyl 4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-[2-(dimethylamino)ethyl-methyl-amino]-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 418.

Step 3: 4-{[2-(dimethylamino)ethyl](methyl)amino}-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 318.

The title compound was synthesized according to General procedure D from 4-{[2-(dimethylamino)ethyl](methyl)amino}-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-chloro-4-methoxylphenyl isocyanate. LCMS [M+H]⁺ 501.

Example 107: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 458.

Example 108: N-(3-chloro-4-methoxyphenyl)-4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

Step 1: tert-butyl 4-[3-(4,6-dihydro-1H-pyrrolo[3,4-c]pyrazol-5-yl)-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from tert-butyl 4-(3-fluoro-2-nitro-anilino)piperidine-1-carboxylate and 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole;dihydrochloride. LCMS [M+H]⁺ 429.

Step 2: tert-butyl 4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-(4,6-dihydro-1H-pyrrolo[3,4-c]pyrazol-5-yl)-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M-isobutene+H]⁺369.

Step 3: 1-(piperidin-4-yl)-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid was synthesized according to General procedure C from tert-butyl 4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 325.

Step 4: The title compound was synthesized according to General procedure D from 1-(piperidin-4-yl)-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-chloro-4-methoxylphenyl isocyanate.

LCMS [M+H]⁺ 508.

Example 109: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5,6-dichloropyridin-3-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 5,6-dichloropyridin-3-amine. LCMS [M+H]⁺ 484.

Example 110: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 6-methoxy-5-methyl-pyridin-3-amine. LCMS [M+H]⁺ 460.

Example 111: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloro-6-methylpyridin-2-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 5-chloro-6-methyl-pyridin-2-amine. LCMS [M+H]⁺ 464.

Example 112: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3,4-dichlorophenyl)-2-methylpiperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(2-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 497.

Example 113: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3,4-dichlorophenyl)-3-methylpiperidine-1-carboxamide

The title compound was synthesized according to General procedure D from 4-bromo-1-(3-methylpiperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 2,2,2-trifluoroacetate and 3,4-dichlorophenyl isocyanate. LCMS [M+H]⁺ 497.

Example 114: 4-(4-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-chloro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 415.

Example 115: N-(3-methoxy-4-methylphenyl)-4-(4-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 395.

Example 116: 4-(4-Methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 411.

Example 117: N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 1-(piperidin-4-yl)-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one;2,2,2-trifluoroacetic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 447.

Example 118: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4-dichloroaniline. LCMS [M+H]⁺ 482. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.83 (br. s., 1H), 7.86 (s, 1H), 7.40-7.45 (m, 2H), 7.35-7.40 (m, 1H), 7.23 (dd, J=8.2, 0.6 Hz, 1H), 7.05 (t, J=8.1 Hz, 1H), 4.39-4.52 (m, 1H), 2.59-2.75 (m, 3H), 2.25 (m, 2H), 1.70-1.93 (m, 4H).

Example 119: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloroaniline. LCMS [M+H]⁺ 448. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.76 (br. s., 1H), 7.49-7.59 (m, 2H), 7.36-7.44 (m, 2H), 7.29-7.36 (m, 2H), 7.14-7.21 (m, 1H), 6.94-7.01 (m, 1H), 4.39-4.52 (m, 1H), 2.61-2.77 (m, 3H), 2.18-2.32 (m, 2H), 1.69-1.90 (m, 4H).

Example 120: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-chloro-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloro-3-(trifluoromethyl)aniline.

LCMS [M+H]⁺ 516. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.89 (s, 1H), 7.93 (d, J=2.5 Hz, 1H), 7.81 (dd, J=8.7, 2.4 Hz, 1H), 7.63 (s, 1H), 7.49 (d, J=8.8 Hz, 1H), 7.37 (d, J=7.9 Hz, 1H), 7.19 (dd, J=8.2, 0.9 Hz, 1H), 6.99 (t, J=8.1 Hz, 1H), 4.40-4.51 (m, 1H), 2.61-2.75 (m, 3H), 2.26 (d, J=14.2 Hz, 2H), 1.73-1.90 (m, 4H).

Example 121: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-fluorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloro-3-fluoroaniline. LCMS [M+H]⁺ 466. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.96 (s, 1H), 7.74 (dd, J=11.1, 2.2 Hz, 1H), 7.54 (br. s., 1H), 7.38 (d, J=7.9 Hz, 1H), 7.32-7.37 (m, 1H), 7.18-7.20 (m, 1H), 7.15-7.18 (m, 1H), 7.01 (t, J=8.1 Hz, 1H), 4.45 (tt, J=12.6, 4.1 Hz, 1H), 2.62-2.74 (m, 3H), 2.19-2.29 (m, 2H), 1.72-1.88 (m, 4H).

Example 122: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloro-3-methoxyaniline. CMS [M+H]⁺ 478. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 9.09 (s, 1H), 7.56 (d, J=2.2 Hz, 1H), 7.51 (br. s., 1H), 7.37 (d, J=8.2 Hz, 1H), 7.30 (d, J=8.5 Hz, 1H), 7.17 (dd, J=8.2, 0.6 Hz, 1H), 6.95 (dd, J=8.2 Hz, 1H), 6.90-6.93 (m, 1H), 4.45 (tt, J=12.5, 4.1 Hz, 1H), 3.95 (s, 3H), 2.60-2.74 (m, 3H), 2.22-2.31 (m, 2H), 1.72-1.88 (m, 4H).

Example 123: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 478. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.82 (s, 1H), 7.65 (d, J=2.5 Hz, 1H), 7.37-7.43 (m, 2H), 7.34 (br. s., 1H), 7.17 (dd, J=8.2, 0.6 Hz, 1H), 6.96-7.01 (m, 1H), 6.92 (d, J=8.8 Hz, 1H), 4.46 (tt, J=12.6, 4.3 Hz, 1H), 3.90 (s, 3H), 2.62-2.75 (m, 3H), 2.20-2.29 (m, 2H), 1.71-1.88 (m, 4H).

Example 124: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4-dimethylaniline. LCMS [M+H]⁺ 442. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.81 (br. s., 1H), 7.39-7.45 (m, 1H), 7.37 (br. s., 1H), 7.24-7.32 (m, 2H), 7.11-7.21 (m, 2H), 6.94-7.01 (m, 1H), 4.43-4.56 (m, 1H), 2.64-2.78 (m, 3H), 2.23-2.33 (m, 8H), 1.72-1.92 (m, 4H).

Example 125: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-cyanophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-amino-2-chlorobenzonitrile. LCMS [M+H]⁺ 473. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.34 (br. s., 1H), 8.00 (br. s., 1H), 7.61-7.69 (m, 2H), 7.51-7.58 (m, 1H), 7.31-7.37 (m, 1H), 7.17-7.23 (m, 1H), 6.98-7.06 (m, 1H), 4.39-4.50 (m, 1H), 2.58-2.77 (m, 3H), 2.20-2.31 (m, 2H), 1.75-1.93 (m, 4H).

Example 126: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxy-3-methylaniline. LCMS [M+H]⁺ 458. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.96 (br. s., 1H), 7.40-7.46 (m, 1H), 7.33-7.39 (m, 1H), 7.22-7.32 (m, 2H), 7.15-7.21 (m, 1H), 6.94-7.01 (m, 1H), 6.80-6.85 (m, 1H), 4.43-4.55 (m, 1H), 3.85 (br. s., 3H), 2.63-2.79 (m, 3H), 2.22-2.32 (m, 5H), 1.72-1.90 (m, 4H).

Example 127: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-phenylcyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and aniline. LCMS [M+H]⁺ 414.

Example 128: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-difluorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4-difluoroaniline. LCMS [M+H]⁺ 450. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.23-8.29 (m, 1H), 7.67-7.76 (m, 1H), 7.39 (d, J=7.9 Hz, 1H), 7.19 (dd, J=8.2, 0.9 Hz, 1H), 7.10-7.17 (m, 2H), 6.98-7.04 (m, 1H), 4.46 (tt, J=12.8, 4.3 Hz, 1H), 2.62-2.75 (m, 3H), 2.20-2.28 (m, 2H), 1.82 (d, J=18.3 Hz, 4H).

Example 129: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methoxy-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxy-3-(trifluoromethyl)aniline.

LCMS [M+H]⁺ 512. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.27 (br. s., 1H), 7.75-7.81 (m, 1H), 7.68 (br. s., 1H), 7.39 (d, J=7.9 Hz, 1H), 7.15-7.24 (m, 2H), 6.95-7.06 (m, 2H), 4.40-4.52 (m, 1H), 3.92 (s, 3H), 2.62-2.75 (m, 3H), 2.22-2.31 (m, 2H), 1.73-1.90 (m, 4H).

Example 130: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-fluoro-3-methoxyaniline. LCMS [M+H]⁺ 462. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.95 (br. s., 1H), 7.49-7.55 (m, 1H), 7.34-7.41 (m, 2H), 7.14-7.20 (m, 1H), 7.01-7.08 (m, 1H), 6.92-6.99 (m, 1H), 6.86-6.92 (m, 1H), 4.39-4.52 (m, 1H), 3.94 (br. s., 3H), 2.62-2.76 (m, 3H), 2.22-2.32 (m, 2H), 1.72-1.90 (m, 4H).

Example 131: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,4-dichlorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2,4-dichloroaniline. LCMS [M+H]⁺ 482

Example 132: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-cyanophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-aminobenzonitrile. LCMS [M+H]⁺ 439.

Example 133: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-(trifluoromethyl)aniline. LCMS [M+H]⁺ 482. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.84 (s, 1H), 7.73 (d, J=8.5 Hz, 2H), 7.63 (d, J=8.5 Hz, 2H), 7.55 (s, 1H), 7.38 (d, J=7.9 Hz, 1H), 7.18 (dd, J=8.2, 0.9 Hz, 1H), 6.96-7.02 (m, 1H), 4.47 (tt, J=12.6, 4.3 Hz, 1H), 2.62-2.76 (m, 3H), 2.23-2.32 (m, 2H), 1.73-1.91 (m, 4H).

Example 134: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-chloro-4-(trifluoromethoxy)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-chloro-4-(trifluoromethoxy)aniline. LCMS [M+H]⁺ 532. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 8.74-8.95 (m, 1H), 7.89 (br. s., 1H), 7.43-7.57 (m, 2H), 7.35-7.41 (m, 1H), 7.28-7.34 (m, 1H), 7.16-7.22 (m, 1H), 6.96-7.05 (m, 1H), 4.39-4.52 (m, 1H), 2.60-2.76 (m, 3H), 2.19-2.30 (m, 2H), 1.72-1.90 (m, 4H).

Example 135: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-aminoindol. LCMS [M+H]⁺ 453.

Example 136: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-fluoroaniline. LCMS [M+H]⁺ 432.

Example 137: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-4-(trifluoromethyl)aniline. LCMS [M+H]⁺ 500. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.87 (d, J=13.3 Hz, 1H), 7.57-7.65 (m, 1H), 7.43-7.49 (m, 2H), 7.16-7.22 (m, 1H), 6.98-7.06 (m, 1H), 4.33-4.46 (m, 1H), 2.65-2.84 (m, 3H), 2.19-2.30 (m, 2H), 1.80-1.92 (m, 2H), 1.64-1.74 (m, 2H).

Example 138: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chlorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-chloroaniline. LCMS [M+H]⁺ 448. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.80 (br. s., 1H), 7.42-7.49 (m, 2H), 7.26-7.33 (m, 1H), 7.14-7.20 (m, 1H), 7.05-7.11 (m, 1H), 6.96-7.03 (m, 1H), 4.32-4.45 (m, 1H), 2.63-2.81 (m, 3H), 2.19-2.29 (m, 2H), 1.77-1.90 (m, 2H), 1.62-1.72 (m, 2H).

Example 139: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methylaniline. LCMS [M+H]⁺ 428. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.40-7.50 (m, 3H), 7.10-7.21 (m, 3H), 6.93-7.03 (m, 1H), 4.33-4.47 (m, 1H), 2.65-2.81 (m, 3H), 2.31 (br. s., 3H), 2.20-2.28 (m, 2H), 1.77-1.90 (m, 2H), 1.62-1.72 (m, 2H).

Example 140: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 444. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.43-7.48 (m, 2H), 7.17 (dd, J=8.2, 0.9 Hz, 1H), 6.95-7.00 (m, 1H), 6.88-6.93 (m, 2H), 4.40 (tt, J=12.8, 4.4 Hz, 1H), 3.78 (s, 3H), 2.65-2.78 (m, 3H), 2.20-2.28 (m, 2H), 1.83 (m, 2H), 1.62-1.71 (m, 2H).

Example 141: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-(trifluoromethyl)aniline.

LCMS [M+H]⁺ 482. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 8.03-8.07 (m, 1H), 7.80-7.85 (m, 1H), 7.49-7.54 (m, 1H), 7.45 (dd, J=7.9, 0.9 Hz, 1H), 7.35-7.40 (m, 1H), 7.18 (dd, J=8.2, 0.9 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 4.40 (tt, J=12.8, 4.4 Hz, 1H), 2.80 (dt, J=4.8, 2.5 Hz, 1H), 2.72-2.78 (m, 1H), 2.65-2.72 (m, 1H), 2.26 (m, 2H), 1.85 (m, 2H), 1.64-1.73 (m, 2H).

Example 142: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-fluoro-3-methylaniline. LCMS [M+H]⁺ 446. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.42-7.47 (m, 2H), 7.35-7.41 (m, 1H), 7.15-7.20 (m, 1H), 6.95-7.03 (m, 2H), 4.39 (tt, J=12.8, 4.5 Hz, 1H), 2.72-2.78 (m, 2H), 2.65-2.71 (m, 1H), 2.20-2.29 (m, 5H), 1.84 (m, 2H), 1.63-1.71 (m, 2H).

Example 143: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methylaniline. LCMS [M+H]⁺ 428. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.43-7.48 (m, 1H), 7.34-7.42 (m, 2H), 7.15-7.24 (m, 2H), 6.90-7.02 (m, 2H), 4.34-4.46 (m, 1H), 2.65-2.81 (m, 3H), 2.34 (br. s., 3H), 2.20-2.29 (m, 2H), 1.78-1.90 (m, 2H), 1.63-1.72 (m, 2H).

Example 144: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methyl-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methyl-3-(trifluoromethyl)aniline.

LCMS [M+H]⁺ 496. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 10.12 (s, 1H), 8.02 (d, J=2.2 Hz, 1H), 7.82 (dd, J=8.4, 2.2 Hz, 1H), 7.40 (d, J=8.2 Hz, 1H), 7.28 (dd, J=8.1, 0.6 Hz, 1H), 7.16 (dd, J=8.1, 0.6 Hz, 1H), 6.96 (t, J=8.1 Hz, 1H), 4.27 (tt, J=12.6, 4.4 Hz, 1H), 2.76 (br. s., 1H), 2.47-2.60 (overlapping m, 2H), 2.40 (br. s, 3H), 2.09-2.20 (m, 2H), 1.69-1.81 (m, 2H), 1.53-1.63 (m, 2H).

Example 145: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-4-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-aminoindol. LCMS [M+H]⁺ 453. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 11.12 (br. s., 1H), 9.59 (s, 1H), 7.51 (d, J=7.3 Hz, 1H), 7.35 (d, J=7.9 Hz, 1H), 7.28-7.31 (m, 1H), 7.18 (d, J=7.9 Hz, 1H), 7.15 (dd, J=8.1, 0.6 Hz, 1H), 7.03-7.08 (m, 1H), 6.96 (t, J=8.1 Hz, 1H), 6.66 (br. t, J=2.2, 2.2 Hz, 1H), 4.31 (tt, J=12.7, 4.5 Hz, 1H), 2.96 (br. s., 1H), 2.57-2.71 (m, 2H), 2.12-2.23 (m, 2H), 1.72-1.85 (m, 2H), 1.53-1.65 (m, 2H).

Example 146: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 414. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.40 (s, 1H), 9.82 (s, 1H), 7.27-7.32 (m, 2H), 7.17 (dd, J=7.9, 1.9 Hz, 1H), 7.06 (dd, J=7.9, 0.9 Hz, 1H), 7.01-7.04 (m, 2H), 4.22-4.34 (m, 1H), 3.79 (s, 3H), 2.74 (br. s., 1H), 2.52-2.62 (m, 2H), 2.14 (m, 2H), 2.10 (s, 3H), 1.68-1.80 (m, 2H), 1.53-1.61 (m, 2H).

Example 147: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 400. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.40 (br. s., 1H), 9.75 (br. s., 1H), 7.55 (br. d, J=7.9 Hz, 2H), 7.25-7.32 (m, 1H), 7.04 (br. s., 2H), 6.91 (br. d, J=8.2 Hz, 2H), 4.22-4.35 (m, 1H), 3.74 (s, 3H), 2.72 (br. s., 1H), 2.53-2.64 (m, 2H), 2.07-2.18 (m, 2H), 1.67-1.80 (m, 2H), 1.51-1.61 (m, 2H).

Example 148: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-aminoindol. LCMS [M+H]⁺ 409. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.41 (s, 1H), 11.01 (s, 1H), 9.78 (s, 1H), 8.00-8.03 (m, 1H), 7.45 (d, J=8.5 Hz, 1H), 7.29-7.34 (m, 1H), 7.27 (dd, J=3.0, 2.4 Hz, 1H), 7.06-7.09 (m, 1H), 7.03-7.05 (m, 2H), 6.36 (ddd, J=3.1, 2.0, 0.9 Hz, 1H), 4.30 (tt, J=12.6, 4.3 Hz, 1H), 2.77 (br. s., 1H), 2.62 (qd, J=12.7, 3.2 Hz, 2H), 2.12-2.20 (m, 2H), 1.70-1.82 (m, 2H), 1.58 (dd, J=9.2, 3.5 Hz, 2H).

Example 149: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methylaniline. LCMS [M+H]⁺ 384. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.40 (s, 1H), 9.80 (s, 1H), 7.51-7.56 (m, 2H), 7.25-7.31 (m, 1H), 7.13 (br. d, J=7.9 Hz, 2H), 7.02-7.07 (m, 2H), 4.28 (tt, J=12.6, 4.2 Hz, 1H), 2.74 (br. s., 1H), 2.53-2.63 (m, 2H), 2.27 (s, 3H), 2.08-2.17 (m, 2H), 1.68-1.80 (m, 2H), 1.52-1.60 (m, 2H).

Example 150: (Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloroaniline. LCMS [M+H]⁺ 404. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.40 (s, 1H), 10.04 (s, 1H), 7.66-7.72 (m, 2H), 7.36-7.41 (m, 2H), 7.23-7.29 (m, 1H), 7.01-7.07 (m, 2H), 4.28 (tt, J=12.5, 4.3 Hz, 1H), 2.76 (br. s., 1H), 2.53-2.62 (m, 2H), 2.10-2.18 (m, 2H), 1.69-1.81 (m, 2H), 1.52-1.63 (m, 2H).

Example 151: Methyl 2-methoxy-5-[(cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexaneamido]benzoate

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and methyl 5-amino-2-methoxybenzoate. LCMS [M+H]⁺ 502. ¹H-NMR (400 MHz, METHANOL-d₄) δ ppm 7.88 (d, J=2.8 Hz, 1H), 7.65 (dd, J=9.0, 2.8 Hz, 1H), 7.34 (dd, J=8.2, 0.9 Hz, 1H), 7.08 (dd, J=8.2, 0.9 Hz, 1H), 7.02 (d, J=9.0 Hz, 1H), 6.88 (t, J=8.2 Hz, 1H), 4.30 (tt, J=12.7, 4.4 Hz, 1H), 3.78 (s, 3H), 3.78 (s, 3H), 2.54-2.70 (m, 3H), 2.11-2.20 (m, 2H), 1.74 (m, 2H), 1.54-1.62 (m, 2H).

Example 152: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-chloro-3-methylaniline. LCMS [M+H]⁺ 462. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 9.95 (s, 1H), 7.64 (d, J=2.2 Hz, 1H), 7.52 (dd, J=8.5, 2.2 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 7.29 (dd, J=8.1, 0.9 Hz, 1H), 7.16 (dd, J=8.1, 0.9 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 4.27 (tt, J=12.5, 4.3 Hz, 1H), 2.75 (br. s., 1H), 2.53-2.61 (m, 2H), 2.33 (s, 3H), 2.09-2.17 (m, 2H), 1.69-1.81 (m, 2H), 1.52-1.62 (m, 2H).

Example 153: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-fluoro-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2-fluoro-4-methylaniline. LCMS [M+H]⁺ 446. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.60 (s, 1H), 7.56 (t, J=8.2 Hz, 1H), 7.27 (dd, J=7.8, 0.8 Hz, 1H), 7.15 (dd, J=8.1, 0.8 Hz, 1H), 7.07-7.13 (m, 1H), 6.99-7.03 (m, 1H), 6.95 (t, J=8.1 Hz, 1H), 4.29 (tt, J=12.5, 4.1 Hz, 1H), 2.83 (br. s., 1H), 2.47-2.60 (overlapping m, 2H), 2.31 (s, 3H), 2.10-2.18 (m, 2H), 1.67-1.79 (m, 2H), 1.51-1.61 (m, 2H).

Example 154: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-difluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2,3-difluoro-4-methoxyaniline. LCMS [M+H]⁺ 480. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.71 (s, 1H), 7.32 (td, J=8.8, 2.5 Hz, 1H), 7.25 (dd, J=8.1, 0.9 Hz, 1H), 7.15 (dd, J=8.1, 0.9 Hz, 1H), 7.03 (td, J=8.8, 2.1 Hz, 1H), 6.94 (t, J=8.1 Hz, 1H), 4.29 (tt, J=12.5, 4.1 Hz, 1H), 3.89 (s, 3H), 2.81 (br. s., 1H), 2.45-2.58 (overlapping m, 2H), 2.10-2.20 (m, 2H), 1.68-1.80 (m, 2H), 1.52-1.62 (m, 2H).

Example 155: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-5-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-5-methoxyaniline. LCMS [M+H]⁺ 462. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 10.06 (s, 1H), 7.28 (dd, J=8.1, 0.6 Hz, 1H), 7.23 (dt, J=11.2, 2.1 Hz, 1H), 7.16 (dd, J=8.1, 0.6 Hz, 1H), 7.04-7.07 (m, 1H), 6.99 (t, J=8.1 Hz, 1H), 6.53 (dt, J=11.2, 2.3 Hz, 1H), 4.27 (tt, J=12.4, 4.2 Hz, 1H), 3.77 (s, 3H), 2.74 (br. s., 1H), 2.46-2.59 (overlapping m, 2H), 2.08-2.17 (m, 2H), 1.69-1.82 (m, 2H), 1.52-1.63 (m, 2H).

Example 156: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2-fluoro-4-methoxyaniline. LCMS [M+H]⁺ 462. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.51 (s, 1H), 7.48 (t, J=9.0 Hz, 1H), 7.24-7.28 (m, 1H), 7.15 (dd, J=8.2, 0.6 Hz, 1H), 6.90-6.97 (m, 3H), 6.79 (ddd, J=8.9, 2.8, 0.9 Hz, 1H), 4.29 (tt, J=12.4, 4.2 Hz, 1H), 3.78 (s, 3H), 2.80 (br. s., 1H), 2.47-2.59 (overlapping m, 2H), 2.15 (m, 2H), 1.67-1.79 (m, 2H), 1.56 (m, 2H).

Example 157: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-cyanophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-chlorobenzonitrile. LCMS [M+H]⁺ 473. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 10.36 (s, 1H), 8.26 (d, J=2.7 Hz, 1H), 7.91 (dd, J=9.0, 2.8 Hz, 1H), 7.72 (d, J=9.0 Hz, 1H), 7.26 (dd, J=8.0, 0.9 Hz, 1H), 7.16 (dd, J=8.1, 0.9 Hz, 1H), 6.99 (t, J=8.2 Hz, 1H), 4.27 (tt, J=12.6, 4.0 Hz, 1H), 2.78 (br. s., 1H), 2.45-2.58 (overlapping m, 2H), 2.11-2.20 (m, 2H), 1.77 (m, 2H), 1.55-1.63 (m, 2H).

Example 158: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-methoxy-5-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methoxy-5-(trifluoromethyl)aniline.

LCMS [M+H]⁺ 512. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 10.20 (s, 1H), 7.67 (br. s, 1H), 7.57 (t, J=1.9 Hz, 1H), 7.27 (dd, J=7.9, 0.6 Hz, 1H), 7.16 (dd, J=8.2, 0.9 Hz, 1H), 6.93-6.99 (m, 2H), 4.27 (tt, J=12.6, 4.0 Hz, 1H), 3.84 (s, 3H), 2.77 (br. s., 1H), 2.45-2.58 (overlapping m, 2H), 2.17 (m, 2H), 1.76 (m, 2H), 1.54-1.63 (m, 2H).

Example 159: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-cyano-3-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-amino-2-methoxybenzonitrile. LCMS [M+H]⁺ 469. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 10.34 (s, 1H), 7.67 (d, J=8.5 Hz, 1H), 7.62 (d, J=1.9 Hz, 1H), 7.40 (dd, J=8.5, 1.9 Hz, 1H), 7.28 (dd, J=8.1, 0.8 Hz, 1H), 7.16 (dd, J=8.1, 0.8 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 4.27 (tt, J=12.5, 4.2 Hz, 1H), 3.92 (s, 3H), 2.80 (br. s., 1H), 2.44-2.58 (overlapping m, 2H), 2.16 (m, 2H), 1.71-1.83 (m, 2H), 1.55-1.63 (m, 2H).

Example 160: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,5-difluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,5-difluoro-4-methoxyaniline. LCMS [M+H]⁺ 480. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (br. s., 1H), 10.15 (br. s., 1H), 7.39-7.50 (m, 2H), 7.27 (d, J=7.3 Hz, 1H), 7.16 (d, J=7.6 Hz, 1H), 6.96-7.03 (m, 1H), 4.21-4.32 (m, 1H), 3.87 (s, 3H), 2.73 (br. s., 1H), 2.44-2.58 (overlapping m, 2H), 2.13 (m, 2H), 1.70-1.82 (m, 2H), 1.53-1.62 (m, 2H).

Example 161: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-cyano-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-methoxybenzonitrile. LCMS [M+H]⁺ 469.

Example 162: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-fluorophenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-chloro-4-fluoroaniline. LCMS [M+H]⁺ 466.

Example 163: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-5-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-chloro-5-methoxyaniline. LCMS [M+H]⁺ 478.

Example 164: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-4-methoxyaniline. LCMS [M+H]⁺ 462.

Example 165: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methoxyaniline. LCMS [M+H]⁺ 444. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 9.88 (s, 1H), 7.33-7.35 (m, 1H), 7.31 (d, J=8.1 Hz, 1H), 7.20-7.26 (m, 2H), 7.16 (dd, J=8.1, 0.6 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 6.61-6.67 (m, 1H), 4.28 (tt, J=12.6, 4.3 Hz, 1H), 3.76 (s, 3H), 2.75 (br. s., 1H), 2.53-2.62 (m, 2H), 2.14 (m, 2H), 1.68-1.80 (m, 2H), 1.52-1.61 (m, 2H).

Example 166: (Cis)-N-(2H-1,3-benzodioxol-5-yl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2H-1,3-benzodioxol-5-amine. LCMS [M+H]⁺ 458. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.80 (s, 1H), 7.36 (d, J=2.2 Hz, 1H), 7.31 (d, J=7.9 Hz, 1H), 7.16 (dd, J=8.2, 0.6 Hz, 1H), 6.96-7.03 (m, 2H), 6.87 (d, J=8.2 Hz, 1H), 6.00 (s, 2H), 4.27 (tt, J=12.6, 4.2 Hz, 1H), 2.71 (br. s., 1H), 2.53-2.62 (m, 2H), 2.06-2.17 (m, 2H), 1.66-1.80 (m, 2H), 1.50-1.60 (m, 2H).

Example 167: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-dimethylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2,3-dimethylaniline. LCMS [M+H]⁺ 442. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.42 (s, 1H), 7.26 (d, J=8.1 Hz, 1H), 7.15 (dd, J=8.1, 0.6 Hz, 1H), 7.07-7.11 (m, 2 H), 7.03-7.07 (m, 1H), 6.94 (t, J=8.1 Hz, 1H), 4.29 (tt, J=12.6, 4.1 Hz, 1H), 2.80 (br. s., 1H), 2.53-2.64 (m, 2H), 2.28 (s, 3H), 2.14-2.22 (m, 2H), 2.11 (s, 3H), 1.70-1.82 (m, 2H), 1.52-1.61 (m, 2H).

Example 168: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-methoxy-5-methylpyridin-3-amine. LCMS [M+H]⁺ 459. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (br. s., 1H), 9.84 (s, 1H), 8.22 (dd, J=2.5, 0.6 Hz, 1H), 7.79 (dd, J=2.5, 0.9 Hz, 1H), 7.29 (dd, J=8.1, 0.6 Hz, 1H), 7.16 (dd, J=8.1, 0.6 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 4.28 (tt, J=12.5, 4.4 Hz, 1H), 3.86 (s, 3H), 2.74 (br. s., 1H), 2.45-2.61 (overlapping m, 2H), 2.17 (d, J=0.6 Hz, 3H), 2.12 (br. s., 2H), 1.69-1.81 (m, 2H), 1.52-1.61 (m, 2H).

Example 169: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-methyl-1,2-oxazol-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-methyl-1,2-oxazol-3-amine. LCMS [M+H]⁺ 419. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 10.89 (s, 1H), 7.25 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 0.9 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 6.75 (s, 1H), 4.26 (tt, J=12.5, 4.1 Hz, 1H), 2.80 (br. s., 1H), 2.42-2.49 (m, 2H), 2.40 (d, J=0.9 Hz, 3H), 2.05-2.15 (m, 2H), 1.66-1.79 (m, 2H), 1.51-1.61 (m, 2H).

Example 170: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-pyrazol-4-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 1-methyl-1H-pyrazol-4-amine. LCMS [M+H]⁺ 418. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.28 (s, 1H), 9.90 (s, 1H), 7.96 (d, J=0.6 Hz, 1H), 7.42 (d, J=0.6 Hz, 1H), 7.30 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 0.9 Hz, 1H), 6.98 (t, J=8.1 Hz, 1H), 4.21-4.31 (m, 1H), 3.81 (s, 3H), 2.65-2.71 (m, 1H), 2.45-2.59 (overlapping m, 2H), 2.06-2.15 (m, 2H), 1.66-1.77 (m, 2H), 1.51-1.60 (m, 2H).

Example 171: (Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-indazol-5-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from (cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 1-methyl-1H-indazol-5-amine. LCMS [M+H]⁺ 468. ¹H-NMR (400 MHz, DMSO-d₆) δ ppm 11.29 (s, 1H), 9.92 (s, 1H), 8.18 (dd, J=1.9, 0.6 Hz, 1H), 8.02 (d, J=0.9 Hz, 1H), 7.60 (dt, J=9.0, 0.9 Hz, 1H), 7.50 (dd, J=9.0, 1.9 Hz, 1H), 7.34 (dd, J=8.1, 0.6 Hz, 1H), 7.16 (dd, J=8.1, 0.6 Hz, 1H), 6.99 (t, J=8.1 Hz, 1H), 4.30 (tt, J=12.6, 4.3 Hz, 1H), 4.03 (s, 3H), 2.78 (br. s., 1H), 2.61 (m, 2H), 2.13-2.21 (m, 2H), 1.70-1.83 (m, 2H), 1.54-1.62 (m, 2H).

Example 172: N-(3-Chloro-4-methoxyphenyl)-4-(5-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 5-methoxy-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 431.

Example 173: N-(3-Chloro-4-methoxyphenyl)-4-(5-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 419.

Example 174: 4-(4-Amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-amino-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 416.

Example 175: N-(3-Chloro-4-methoxyphenyl)-4-[2-oxo-4-(propylamino)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

Step 1: N-benzyl-3-fluoro-2-nitro-N-propyl-aniline was synthesized according to General procedure A from 1,3-difluoro-2-nitrobenzene and N-benzylpropylamine. LCMS [M+H]⁺ 289.

Step 2: tert-butyl 4-[3-[benzyl(propyl)amino]-2-nitro-anilino]piperidine-1-carboxylate was synthesized according to General procedure A from N-benzyl-3-fluoro-2-nitro-N-propyl-aniline and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 469.

Step 3: tert-butyl 4-[4-[benzyl(propyl)amino]-2-oxo-3H-benzimidazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[3-[benzyl(propyl)amino]-2-nitro-anilino]piperidine-1-carboxylate. LCMS [M+H]⁺ 465

Step 4: tert-butyl 4-[2-oxo-4-(propylamino)-3H-benzimidazol-1-yl]piperidine-1-carboxylate was synthesized according to General procedure G from tert-butyl 4-[4-[benzyl(propyl)amino]-2-oxo-3H-benzimidazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 375. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 10.97 (br. s., 1H), 6.98 (t, J=8.1 Hz, 1H), 6.62 (d, J=8.2 Hz, 1H), 6.48 (d, J=7.9 Hz, 1H), 4.19-4.45 (m, 3H), 3.22 (t, J=7.0 Hz, 2H), 2.84 (br. s., 2H), 2.27-2.40 (m, 2H), 1.70-1.84 (m, 4H), 1.51 (s, 9H), 1.07 (t, J=7.4 Hz, 3H).

Step 5: 1-(piperidin-4-yl)-4-(propylamino)-2,3-dihydro-1H-1,3-benzodiazol-2-one was synthesized according to General procedure G from tert-butyl 4-[2-oxo-4-(propylamino)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxylate. LCMS [M+H]⁺ 275.

Step 5: the title compound was synthesized according to General procedure C from 1-(piperidin-4-yl)-4-(propylamino)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 458.

Example 176: N-(3-Chloro-4-methoxyphenyl)-4-[4-(methylsulfanyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-(methylsulfanyl)-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 447.

Example 177: 4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)-3-hydroxypiperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-bromo-1-(3-hydroxypiperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 495.

Example 178: N-(3-Chloro-4-methoxyphenyl)-4-(5-cyano-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 2-oxo-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazole-5-carbonitrile and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 426.

Example 179: N-(3-Chloro-4-methoxyphenyl)-4-(5-methyl-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 5-methyl-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 415.

Example 180: N-(3-Chloro-4-methoxyphenyl)-4-{7-methyl-2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-3-yl}piperidine-1-carboxamide

Step 1: tert-butyl 4-[(4-methyl-3-nitro-2-pyridyl)amino]piperidine-1-carboxylate was synthesized according to General procedure A from 2-chloro-4-methyl-3-nitro-pyridine and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 337.

Step 2: tert-butyl 4-(7-methyl-2-oxo-1H-imidazo[4,5-b]pyridin-3-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[(4-methyl-3-nitro-2-pyridyl)amino]piperidine-1-carboxylate. LCMS [M+H]⁺ 333. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 10.10 (br. s., 1H), 7.94 (d, J=5.4 Hz, 1H), 6.84 (dd, J=5.2, 0.8 Hz, 1H), 4.58 (tt, J=12.1, 4.0 Hz, 1H), 4.31 (br. s., 2H), 2.87 (br. s., 2H), 2.59-2.72 (m, 2H), 2.41 (s, 3H), 1.75-1.85 (m, 2H), 1.50 (s, 9H).

Step 3: 7-methyl-3-(4-piperidyl)-1H-imidazo[4,5-b]pyridin-2-one was synthesized according to General procedure C from tert-butyl 4-(7-methyl-2-oxo-1H-imidazo[4,5-b]pyridin-3-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 233. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.31 (s, 1H), 8.82-8.95 (m, 1H), 8.41-8.56 (m, 1H), 7.83 (d, J=5.4 Hz, 1H), 6.88 (dd, J=5.4, 0.6 Hz, 1H), 4.53-4.64 (m, 1H), 3.37-3.40 (m, 2H), 3.05-3.18 (m, 2H), 2.67-2.82 (m, 2H), 2.30 (s, 3H), 1.82-1.92 (m, 2H).

Step 4: the title compound was synthesized according to General procedure I from 7-methyl-3-(4-piperidyl)-1H-imidazo[4,5-b]pyridin-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 416.

Example 181: N-(3-Chloro-4-methoxyphenyl)-4-{6-methyl-2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-3-yl}piperidine-1-carboxamide

Step 1: tert-butyl 4-[(5-methyl-3-nitro-2-pyridyl)amino]piperidine-1-carboxylate was synthesized according to General procedure A from 2-chloro-5-methyl-3-nitro-pyridine and tert-butyl 4-aminopiperidine-1-carboxylate. LCMS [M+H]⁺ 337.

Step 2: tert-butyl 4-(6-methyl-2-oxo-1H-imidazo[4,5-b]pyridin-3-yl)piperidine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[(5-methyl-3-nitro-2-pyridyl)amino]piperidine-1-carboxylate. LCMS [M+H]⁺ 333. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 9.46 (br. s., 1H), 7.86 (dd, J=1.9, 0.9 Hz, 1H), 7.17 (d, J=1.3 Hz, 1H), 4.55 (tt, J=12.1, 4.0 Hz, 1H), 4.20-4.40 (m, 2H), 2.60-2.80 (m, 2H), 2.64-2.73 (m, 2H), 2.36 (s, 3H), 1.74-1-84 (m, 2H), 1.51 (s, 9H).

Step 3: 6-methyl-3-(4-piperidyl)-1H-imidazo[4,5-b]pyridin-2-one was synthesized according to General procedure C from tert-butyl 4-(6-methyl-2-oxo-1H-imidazo[4,5-b]pyridin-3-yl)piperidine-1-carboxylate. LCMS [M+H]⁺ 233. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.14 (s, 1H), 8.91 (br. s., 1H), 8.42-8.56 (m, 1H), 7.77 (s, 1H), 7.17 (d, J=0.6 Hz, 1H), 4.51-4.62 (m, 1H), 3.40 (br. s., 2H), 3.05-3.18 (m, 2H), 2.67-2.80 (m, 2H), 2.29 (s, 3H), 1.82-1.92 (m, 2H).

Step 4: the title compound was synthesized according to General procedure I from and 3-chloro-4-methoxyaniline. LCMS [M+H]⁺ 416.

Example 182: N-(3-Chloro-4-methoxyphenyl)-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 4-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-chloro-4-methoxyaniline.

LCMS [M+H]⁺ 419.

Example 183: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxypyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-methoxypyridine. LCMS [M+H]⁺ 445.

Example 184: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-chloropyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-chloropyridine. LCMS [M+H]⁺ 449.

Example 185: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5,6-dichloropyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2,3-dichloropyridine. LCMS [M+H]⁺ 483.

Example 186: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indazol-7-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 7-amino-1H-indazole. LCMS [M+H]⁺ 454.

Example 187: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-chloro-5-methylpyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-chloro-3-methylpyridine. LCMS [M+H]⁺ 463.

Example 188: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloropyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-amino-5-chloropyridine. LCMS [M+H]⁺ 449.

Example 189: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-methylpyridin-2-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2-amino-5-methylpyridine. LCMS [M+H]⁺ 429.

Example 190: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methylpyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-methylpyridine. LCMS [M+H]⁺ 429.

Example 191: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-hydroxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-aminophenol. LCMS [M+H]⁺ 430.

Example 192: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4-dimethoxyaniline. LCMS [M+H]⁺ 474.

Example 193: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4,5-trimethoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4,5-trimethoxyaniline. LCMS [M+H]⁺ 504.

Example 194: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-hydroxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-amino-2-methylphenol. LCMS [M+H]⁺ 444.

Example 195: Cis-N-(3-aminophenyl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and m-phenylenediamine. LCMS [M+H]⁺ 429.

Example 196: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-hydroxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-aminophenol. LCMS [M+H]⁺ 430.

Example 197: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-dihydro-1,4-benzodioxin-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2,3-dihydro-1,4-benzodioxin-6-amine. LCMS [M+H]⁺ 472.

Example 198: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(dimethylamino)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and N,N-dimethyl-m-phenylenediamine. LCMS [M+H]⁺ 457.

Example 199: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methyl-1H-indazol-5-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-3-methyl-1H-indazole. LCMS [M+H]⁺ 468.

Example 200: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-(dimethylamino)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and N,N-dimethyl-p-phenylenediamine. LCMS [M+H]⁺ 457.

Example 201: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-hydroxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-amino-2-chlorophenol. LCMS [M+H]⁺ 464.

Example 202: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloro-6-methoxypyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-3-chloro-2-methoxypyridine. LCMS [M+H]⁺ 479.

Example 203: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-methyl-1,3-benzoxazol-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-amino-2-methyl-1,3-benzoxazole. LCMS [M+H]⁺ 469.

Example 204: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(quinolin-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-amino-quinoline. LCMS [M+H]⁺ 465.

Example 205: Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 396.

Example 206: Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxy-3-methylaniline. LCMS [M+H]⁺ 410.

Example 207: Cis-N-(3-fluoro-4-methoxyphenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-4-methoxyaniline. LCMS [M+H]⁺ 414.

Example 208: Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-amino-2-methoxy-3-methylpyridine. LCMS [M+H]⁺ 411.

Example 209: Cis-N-(1H-indol-6-yl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-amino-1H-indole. LCMS [M+H]⁺ 405.

Example 210: N-(3-Methoxy-4-methylphenyl)-4-(2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide

The title compound was synthesized according to General procedure I from 1-(piperidin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-2-one and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 381.

Example 211: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 384.

Example 212: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxy-3-methylaniline. LCMS [M+H]⁺ 398.

Example 213: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-4-methoxyaniline. LCMS [M+H]⁺ 402.

Example 214: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-methoxy-3-methylpyridine. LCMS [M+H]⁺ 399.

Example 215: Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 6-amino-1H-indole. LCMS [M+H]⁺ 393.

Example 216: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 384.

Example 217: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-methoxy-3-methylaniline. LCMS [M+H]⁺ 398.

Example 218: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-fluoro-4-methoxyaniline. LCMS [M+H]⁺ 402.

Example 219: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 398.

Example 220: Cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-hydroxy-3-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(6-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-amino-2-methylphenol. LCMS [M+H]⁺ 384.

Example 221: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-hydroxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 5-amino-2-methylphenol. LCMS [M+H]⁺ 444.

Example 222: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-hydroxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2-amino-5-methylphenol. LCMS [M+H]⁺ 444.

Example 223: Cis-N-(2-amino-4,5-dimethylphenyl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3,4-dimethyl-o-phenylenediamine. LCMS [M+H]⁺ 457.

Example 224: 4-[cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexaneamido]benzamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 4-aminobenzamide. LCMS [M+H]⁺ 457.

Example 225: Cis-4-(4-{3-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure E from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and dimethyl-(2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-ethyl)-amine. LCMS [M+H]⁺ 543.

Example 226: Cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

A mixture of cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.) and Pd/C (0.20 equiv.) was stirred in a mixture of 1,4-dioxane and cyclohexene under nitrogen atmosphere at 100° C. for 20 h. The mixture was then purified by silica gel chromatography using EtOAc as eluent.

LCMS [M+H]⁺ 380.

Example 227: Cis-4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

A mixture of cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolane (3.0 equiv.), KOAc (3.0 equiv.), and Pd(dppf) (0.15 equiv.) was stirred in 1,4-dioxane at 100° C. for 20 h. After cooling the reaction mixture to 20° C., H₂O₂ (30 wt % in H₂O, 6 equiv.) was added and the resulting mixture was stirred at 20° C. for 16 h. The mixture was then concentrated and purified by preparative HPLC. LCMS [M+H]⁺ 396.

Example 228: N-[2-(Dimethylamino)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and N,N-dimethyl-1,2-ethylenediamine. LCMS [M+H]⁺ 494.

Example 229: Cis-4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: 4-[3-[2-(dimethylamino)ethyl-methyl-amino]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N,N′,N′-trimethylethylene-1,2-diamine.

LCMS [M+H]⁺ 484. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.43 (d, J=1.6 Hz, 1H), 7.36 (s, 1H), 7.20 (t, J=8.2 Hz, 1H), 7.03 (d, J=8.5 Hz, 1H), 6.77 (dd, J=7.9, 2.2 Hz, 1H), 6.34-6.41 (m, 2H), 6.23 (d, J=7.0 Hz, 1H), 3.84 (s, 3H), 3.63-3.72 (m, 1H), 3.47 (m, 2H), 2.92-2.97 (m, 2H), 2.79 (s, 3H), 2.58-2.67 (m, 6H), 2.39-2.47 (m, 1H), 2.17 (s, 3H), 1.71-1.99 (m, 8H).

Step 2: the title compound was synthesized according to General procedure B from 4-[3-[2-(dimethylamino)ethyl-methyl-amino]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 480.

Example 230: Cis-N-(3-methoxy-4-methylphenyl)-4-(4-{[(4-methoxyphenyl)methyl]sulfanyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

Step 1: a mixture of cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate (1.0 equiv.), 4-methoxybenzyl mercaptane (1.1 equiv.), and N,N-diisopropylethylamine (1.3 equiv.) in methanol was stirred at 70° C. for 16 h. The resulting mixture was concentrated and purified by silica gel chromatography which afforded methyl cis-4-[3-[(4-methoxyphenyl)methylsulfanyl]-2-nitro-anilino]cyclohexanecarboxylate. LCMS [M+H]⁺ 297.

Step 2: methyl cis-4-[4-[(4-methoxyphenyl)methylsulfanyl]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate was synthesized according to General procedure B from methyl cis-4-[3-[(4-methoxyphenyl)methylsulfanyl]-2-nitro-anilino]cyclohexanecarboxylate. LCMS [M+H]⁺ 427.

Step 3: cis-4-[4-[(4-methoxyphenyl)methylsulfanyl]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid was synthesized according to General procedure J from methyl cis-4-[4-[(4-methoxyphenyl)methylsulfanyl]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate. LCMS [M+H]⁺ 413.

Step 4: the title compound was synthesized according to General procedure H from cis-4-[4-[(4-methoxyphenyl)methylsulfanyl]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 532.

Example 231: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(hydroxymethyl)phenyl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 3-aminobenzyl alcohol. LCMS [M+H]⁺ 444.

Example 232: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 381. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.55 (br. s., 1H), 9.83 (s, 1H), 7.90 (d, J=5.4 Hz, 1H), 7.53-7.57 (m, 1H), 7.28 (s, 1H), 7.16-7.20 (m, 1H), 7.00-7.09 (m, 2H), 4.24-4.36 (m, 1H), 3.79 (s, 3H), 2.70-2.77 (m, 1H), 2.44-2.57 (m overlapping with solvent signal, 2H), 2.07-2.17 (m, 5H), 1.68-1.80 (m, 2H), 1.50-1.65 (m, 2H).

Example 233: Cis-N-(4-methoxy-3-methylphenyl)-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylic acid and 4-methoxy-3-methylaniline. LCMS [M+H]⁺ 381.

Example 234: Cis-N-(4-methoxyphenyl)-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylic acid and 4-methoxyaniline. LCMS [M+H]⁺ 367. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.51-11.58 (m, 1H), 9.76 (s, 1H), 7.89 (dd, J=5.2, 1.4 Hz, 1H), 7.51-7.56 (m, 3H), 7.04 (dd, J=7.7, 5.2 Hz, 1H), 6.87-6.92 (m, 2H), 4.24-4.35 (m, 1H), 3.73 (s, 3H), 2.71 (br. s., 1H), 2.45-2.58 (m overlapping with solvent signal, 2H), 2.07-2.15 (m, 2H), 1.67-1.78 (m, 2H), 1.52-1.62 (m, 2H).

Example 235: Cis-N-(6-methoxy-5-methylpyridin-3-yl)-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-{2-oxo-1H,2H,3H-imidazo[4,5-b]pyridin-1-yl}cyclohexane-1-carboxylic acid and 5-amino-2-methoxy-3-methylpyridine. LCMS [M+H]⁺ 382. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.56 (br. s., 1H), 9.85 (s, 1H), 8.23 (s, 1H), 7.90 (d, J=5.1 Hz, 1H), 7.79 (s, 1H), 7.50-7.55 (m, 1H), 7.02-7.08 (m, 1H), 4.24-4.36 (m, 1H), 3.86 (s, 3H), 2.71-2.77 (m, 2H), 2.43-2.56 (m overlapping with solvent signal, 2H), 2.08-2.19 (m, 5H), 1.69-1.81 (m, 2H), 1.54-1.64 (m, 2H).

Example 236: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-1H,2H,3H-imidazo[4,5-c]pyridin-1-yl}cyclohexane-1-carboxamide

Step 1: methyl cis-4-[(2-nitro-4-pyridyl)amino]cyclohexanecarboxylate was synthesized according to General procedure A from 4-chloro-3-nitro-pyridine and methyl cis-4-aminocyclohexanecarboxylate.

LCMS [M+H]⁺ 280.

Step 2: methyl cis-4-(2-oxo-3H-imidazo[4,5-c]pyridin-1-yl)cyclohexanecarboxylate was synthesized according to General procedure F from methyl cis-4-[(2-nitro-4-pyridyl)amino]cyclohexanecarboxylate. LCMS [M+H]⁺ 276.

Step 3: cis-4-[-oxo-3H-imidazo[4,5-c]pyridin-1-yl]cyclohexanecarboxylic acid was synthesized according to General procedure J from methyl cis-4-(2-oxo-3H-imidazo[4,5-c]pyridin-1-yl)cyclohexanecarboxylate. LCMS [M+H]⁺ 262.

Step 4: the title compound was synthesized according to General procedure H from cis-4-[2-oxo-3H-imidazo[4,5-c]pyridin-1-yl]cyclohexanecarboxylic acid. LCMS [M+H]⁺ 382. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 12.28 (s, 1H), 9.87 (s, 1H), 8.56-8.60 (m, 2H), 7.77 (d, J=6.3 Hz, 1H), 7.28 (d, J=1.9 Hz, 1H), 7.20 (dd, J=7.9, 1.9 Hz, 1H), 7.04-7.08 (m, 1H), 4.35-4.45 (m, 1H), 3.79 (s, 3H), 2.73-2.78 (m, 1H), 2.52-2.61 (m, 2H), 2.12-2.18 (m, 2H), 2.11 (s, 3H), 1.72-1.83 (m, 2H), 1.63-1.72 (m, 2H).

Example 237: Cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-4-sulfanyl-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

A mixture of N-(4-methoxy-3-methyl-phenyl)-4-[4-[(4-methoxyphenyl)methylsulfanyl]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxamide (1.0 equiv.) and anisole (2.0 equiv.) was stirred in TFA at 80° C. The mixture was then poured into NaHCO₃ (aq.) and extracted with DCM×3. The combined organics were concentrated and purified using preparative HPLC. LCMS [M+H]⁺ 412.

Example 238: Cis-4-(5-cyano-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: methyl 4-(4-cyano-2-nitro-anilino)cyclohexanecarboxylate was synthesized according to General procedure A from 4-chloro-3-nitrobenzonitrile and methyl cis-4-aminocyclohexanecarboxylate. LCMS [M+H]⁺ 304.

Step 2: methyl cis-4-(5-cyano-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate was synthesized according to General procedure F from methyl 4-(4-cyano-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 300. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 10.28 (s, 1H), 7.37-7.43 (m, 2H), 7.28-7.33 (m, 1H), 4.38-4.50 (m, 1H), 3.80 (s, 3H), 2.81 (m, 1H), 2.25-2.47 (m, 4H), 1.69-1.83 (m, 4H).

Step 3: cis-4-(5-cyano-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylic acid was synthesized according to General procedure J from methyl cis-4-(5-cyano-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate. LCMS [M+H]⁺ 286. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 12.36 (s, 1H), 11.33 (s, 1H), 7.49 (dd, J=8.2, 1.6 Hz, 1H), 7.37 (d, J=1.3 Hz, 1H), 7.25 (d, J=8.2 Hz, 1H), 4.23 (tt, J=12.4, 3.8 Hz, 1H), 2.63-2.69 (m, 1H), 2.19-2.31 (m, 2H), 2.11-2.19 (m, 2H), 1.57-1.70 (m, 4H).

Step 4. The title compound was synthesized according to General procedure H from cis-4-(5-cyano-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 405. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.34 (br. s., 1H), 9.83 (s, 1H), 7.50-7.55 (m, 1H), 7.43-7.47 (m, 1H), 7.38 (d, J=1.3 Hz, 1H), 7.31 (d, J=1.9 Hz, 1H), 7.16 (dd, J=8.1, 1.7 Hz, 1H), 7.06 (d, J=8.2 Hz, 1H), 4.25-4.36 (m, 1H), 3.79 (s, 3H), 2.70-2.76 (m, 1H), 2.53-2.62 (m, 2H), 2.11-2.17 (m, 2H), 2.11 (s, 3H), 1.69-1.81 (m, 2H), 1.53-1.63 (m, 2H).

Example 239: 2-({2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}sulfonyl)acetic acid

Step 1: a mixture of cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-4-sulfanyl-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide (1.0 equiv.), diisopropylethylamine (1.1 equiv.), and ethyl bromoacetate (1.0 equiv.) was stirred in THE at 40° C. for 16 h. The mixture was then poured into NaHCO₃ (aq.) and extracted with DCM×3. The combined extracts were dried, concentrated, and purified by silica gel chromatography.

LCMS [M+H]⁺ 526.

Step 2: a mixture of tert-butyl 2-[[1-[4-[(4-methoxy-3-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]sulfanyl]acetate (1.0 equiv.) and 3-chloroperbenzoic acid (2.1 equiv.) was stirred in DCM at 20° C. for 30 min. The mixture was then poured into NaHCO₃ (aq.) and extracted with DCM×3. The combined extracts were dried, concentrated, and purified by silica gel chromatography. LCMS [M+H]⁺ 556.

Step 3: tert-butyl 2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]sulfonyl]acetate (1.0 equiv.) was dissolved in DCM, then TFA (10 equiv.) was added. The resulting mixture was stirred at 20° C. for 16 h after which the mixture was purified by silica gel chromatography. LCMS [M+H]⁺ 502. ¹H-NMR (400 MHz, Methanol-d4) δ ppm 7.80 (d, J=7.9 Hz, 1H), 7.50 (d, J=7.9 Hz, 1H), 7.35 (dd, J=8.8, 2.5 Hz, 1H), 7.29 (d, J=2.2 Hz, 1H), 7.26 (t, J=8.0 Hz, 1H), 6.88 (d, J=8.5 Hz, 1H), 4.39-4.51 (m, 1H), 4.34 (br. s, 2H), 3.82 (s, 3H), 2.68-2.82 (m, 3H), 2.22-2.30 (m, 2H), 2.20 (s, 3H), 1.80-1.92 (m, 2H), 1.66-1.74 (m, 2H).

Example 240: Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperazin-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: tert-butyl 4-[cis-1-(4-methoxycarbonylcyclohexyl)-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate was synthesized according to General procedure A from cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate and tert-butyl piperazine-1-carboxylate. LCMS [M+H]⁺ 463.

Step 2: tert-butyl 4-[cis-1-(4-methoxycarbonylcyclohexyl)-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate was synthesized according to General procedure B from tert-butyl 4-[1-(4-methoxycarbonylcyclohexyl)-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate. LCMS [M+H]⁺ 459.

Step 3: cis-4-[4-(4-tert-butoxycarbonylpiperazin-1-yl)-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid was synthesized according to General procedure J from tert-butyl 4-[cis-1-(4-methoxycarbonylcyclohexyl)-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate. LCMS [M+H]⁺ 445.

Step 4: tert-butyl 4-[1-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate was synthesized according to General procedure H from cis-4-[4-(4-tert-butoxycarbonylpiperazin-1-yl)-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 564.

Step 5: the title compound was synthesized according to General procedure C from tert-butyl 4-[1-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]piperazine-1-carboxylate. LCMS [M+H]⁺ 464

Example 241: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(morpholin-4-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: methyl 4-(3-morpholino-2-nitro-anilino)cyclohexanecarboxylate was synthesized according to General procedure A from Cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate and morpholine. LCMS [M+H]⁺ 364.

Step 2: methyl cis-4-(4-morpholino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate was synthesized according to General procedure B from methyl cis-4-(3-morpholino-2-nitro-anilino)cyclohexanecarboxylate. LCMS [M+H]⁺ 360.

Step 3: cis-4-(4-morpholino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylic acid was synthesized according to General procedure B from methyl cis-4-(4-morpholino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylate. LCMS [M+H]⁺ 346.

Step 4: the title compound was synthesized according to General procedure H from cis-4-(4-morpholino-2-oxo-3H-benzimidazol-1-yl)cyclohexanecarboxylic acid and 3-methoxy-4-methylaniline.

LCMS [M+H]⁺ 465.

Example 242: 2-({2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}oxy)acetic acid

Step 1: to a mixture of cis-4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.) and tert-butyl bromoacetate (1.1 equiv.) in THE was added NaH (1.0 equiv.). The resulting mixture was stirred for 4 days at 40° C. after which it was concentrated and purified by silica gel chromatography which afforded tert-butyl 2-[[1-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]oxy]acetate. LCMS [M+H]⁺ 468.

Step 2: tert-butyl 2-[[1-[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]oxy]acetate (1.0 equiv.) was dissolved in DCM, then TFA (10 equiv.) was added and the resulting mixture was stirred for 6 h. The mixture was concentrated and purified by preparative HPLC. LCMS [M+H]⁺ 454.

Example 243: Cis-4-{4-[benzyl(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: methyl cis-4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate was synthesized according to general procedure A from cis-4-[(3-fluoro-2-nitrophenyl)amino]cyclohexane-1-carboxylate and N-methylbenzylamine.

LCMS [M+H]⁺ 398.

Step 2: methyl 4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate was synthesized according to general procedure B from methyl cis-4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate. LCMS [M+H]⁺ 394.

Step 3: cis-4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid was synthesized according to general procedure J from methyl 4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylate.

Step 4: the title compound was synthesized according to general procedure H from cis-4-[4-[benzyl(methyl)amino]-2-oxo-3H-benzimidazol-1-yl]cyclohexanecarboxylic acid. LCMS [M+H]⁺ 499. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.83 (s, 1H), 9.79 (s, 1H), 7.25-7.30 (m, 5H), 7.19-7.23 (m, 1H), 7.17 (dd, J=8.1, 1.7 Hz, 1H), 7.05 (d, J=7.9 Hz, 1H), 6.98 (d, J=7.9 Hz, 1H), 6.86 (t, J=8.1 Hz, 1H), 6.58 (d, J=8.2 Hz, 1H), 4.22-4.32 (m, 1H), 4.20 (s, 2H), 3.78 (s, 3H), 3.57 (s, 1H), 2.70-2.75 (m, 1H), 2.54-2.63 (m, 5H), 2.11-2.18 (m, 2H), 2.09 (s, 3H), 1.67-1.78 (m, 2H), 1.50-1.59 (m, 2H).

Example 244: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure G from cis-4-{4-[benzyl(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide. LCMS [M+H]⁺ 409. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.25 (s, 1H), 9.78 (s, 1H), 7.28 (d, J=1.9 Hz, 1H), 7.16 (dd, J=7.9, 1.9 Hz, 1H), 7.05 (dd, J=8.1, 0.8 Hz, 1H), 6.82-6.88 (m, 1H), 6.73 (d, J=7.9 Hz, 1H), 6.31 (d, J=8.2 Hz, 1H), 4.16-4.27 (m, 1H), 2.79 (s, 3H), 2.69-2.74 (m, 1H), 2.52-2.61 (m, 2H), 2.10-2.17 (m, 2H), 2.09 (s, 3H), 1.65-1.77 (m, 2H), 1.46-1.55 (m, 2H).

Example 245: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure H from cis-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxylic acid and 3-methoxy-4-methylaniline. LCMS [M+H]⁺ 454.

Example 246: Cis-N-(1H-indol-6-yl)-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure H from cis-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxylic acid and 6-amino-1H-indole. LCMS [M+H]⁺ 449. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.97-11.01 (m, 1H), 10.91 (s, 1H), 9.77 (s, 1H), 7.99-8.01 (m, 1H), 7.42 (d, J=8.5 Hz, 1H), 7.25 (dd, J=3.0, 2.4 Hz, 1H), 7.06 (dd, J=8.5, 1.9 Hz, 1H), 6.89-6.97 (m, 2H), 6.71 (d, J=1.6 Hz, 1H), 6.34 (s, 1H), 4.12-4.22 (m, 3H), 3.67-3.71 (m, 2H), 3.33 (s, 3H), 2.44-2.50 (m, 1H), 2.20-2.32 (m, 2H), 1.96-2.04 (m, 2H), 1.75-1.83 (m, 2H), 1.62-1.75 (m, 2H).

Example 247: N-(2-Aminoethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to general procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 1,2-ethylenediamine. LCMS [M+H]⁺ 466.

Example 248: N-(2,3-Dihydroxypropyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to general procedure L from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (±)-3-amino-1,2-propanediol. LCMS [M+H]⁺ 497.

Example 249: Cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: cis-4-[3-(dibenzylamino)-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to general procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and dibenzylamine. LCMS [M+H]⁺ 579.

Step 2: cis-4-[4-(dibenzylamino)-2-oxo-3H-benzimidazol-1-yl]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to general procedure B from cis-4-[3-(dibenzylamino)-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 575.

Step 3: The title compound was synthesized according to general procedure G from cis-4-[4-(dibenzylamino)-2-oxo-3H-benzimidazol-1-yl]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 395. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.25 (s, 1H), 9.77 (s, 1H), 7.28 (d, J=1.6 Hz, 1H), 7.15 (dd, J=8.2, 1.9 Hz, 1H), 7.05 (dd, J=8.2, 0.9 Hz, 1H), 6.71 (t, J=8.2 Hz, 1H), 6.61 (d, J=7.9 Hz, 1H), 6.30 (dd, J=8.1, 0.9 Hz, 1H), 4.20 (tt, J=12.4, 4.2 Hz, 1H), 3.77 (s, 3H), 2.71 (br. s., 1H), 2.52-2.60 (m, 2H), 2.08-2.14 (m, 2H), 2.09 (s, 3H), 1.64-1.76 (m, 2H), 1.45-1.55 (m, 2H).

Example 250: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(2-methoxyacetamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

A mixture of cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), diisopropylethylamine (2.0 equiv.), and 2-methoxyacetyl chloride (1.0 equiv.) was stirred in 1,4-dioxane for 16 h. The mixture was then concentrated and purified by preparative HPLC. LCMS [M+H]⁺ 467. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.59 (s, 1H), 9.81 (s, 1H), 9.49 (s, 1H), 7.28-7.33 (m, 1H), 7.14-7.20 (m, 2H), 7.03-7.10 (m, 2H), 6.92-6.99 (m, 1H), 4.21-4.33 (m, 2H), 4.02 (s, 2H), 3.79 (s, 3H), 3.41 (s, 3H), 2.71-2.77 (m, 1H), 2.54-2.65 (m, 2H), 2.12-2.20 (m, 2H), 2.11 (s, 3H), 1.67-1.80 (m, 2H), 1.51-1.61 (m, 2H).

Example 251: N-(2-Methanesulfonamidoethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to general procedure L from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N-(2-aminoethyl)methanesulfonamide.

LCMS [M+H]⁺ 544. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.51 (s, 1H), 9.83 (s, 1H), 8.51-8.56 (m, 1H), 7.46 (d, J=7.9 Hz, 1H), 7.39-7.43 (m, 1H), 7.31 (d, J=1.9 Hz, 1H), 7.16-7.20 (m, 2H), 7.05-7.11 (m, 2H), 4.25-4.37 (m, 1H), 3.79 (s, 3H), 3.36-3.42 (m, 2H), 3.10-3.17 (m, 2H), 2.92 (s, 3H), 2.71-2.77 (m, 1H), 2.53-2.65 (m, 2H), 2.12-2.18 (m, 2H), 2.11 (s, 3H), 1.69-1.81 (m, 2H), 1.51-1.60 (m, 2H).

Example 252: 2-Oxo-N-[2-(piperazin-1-yl)ethyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: tert-butyl cis-4-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]ethyl]piperazine-1-carboxylate was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1-tert-butoxycarbonyl-4-(2-aminoethyl)piperazine and was used in step 2 without purification.

Step 2: the title compound was synthesized according to General procedure C from tert-butyl cis-4-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]ethyl]piperazine-1-carboxylate. LCMS [M+H]⁺ 535. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.55 (s, 1H), 9.84 (s, 1H), 8.58-8.66 (m, 1H), 7.48 (d, J=7.9 Hz, 1H), 7.39 (d, J=7.9 Hz, 1H), 7.30 (d, J=1.9 Hz, 1H), 7.18 (dd, J=7.9, 1.9 Hz, 1H), 7.10 (t, J=7.9 Hz, 1H), 7.06 (dd, J=8.1, 0.8 Hz, 1H), 4.25-4.37 (m, 1H), 3.79 (s, 3H), 3.50-3.59 (m, 2H), 3.24-3.36 (m, 4H), 2.86-3.24 (m, 6H), 2.72-2.77 (m, 1H), 2.54-2.65 (m, 2H), 2.12-2.19 (m, 2H), 2.11 (s, 3H), 1.70-1.81 (m, 2H), 1.52-1.61 (m, 2H).

Example 253: Cis-4-{4-[(2-acetamidoethyl)carbamoyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure L from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N-(2-aminoethyl)acetamide. LCMS [M+H]⁺ 508. ¹H-NMR (400 MHz, Methanol-d4) δ ppm 7.65 (d, J=7.9 Hz, 1H), 7.43 (d, J=7.9 Hz, 1H), 7.25-7.29 (m, 1H), 7.13 (t, J=8.1 Hz, 1H), 7.06-7.10 (m, 1H), 7.01-7.05 (m, 1H), 4.39-4.51 (m, 1H), 3.87 (s, 3H), 3.48-3.55 (m, 2H), 3.39-3.46 (m, 2H), 2.69-2.83 (m, 3H), 2.23-2.32 (m, 2H), 2.17 (s, 3H), 1.96 (s, 2H), 1.80-1.93 (m, 2H), 1.65-1.75 (m, 2H).

Example 254: 2-Oxo-N-[(pyrrolidin-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: tert-butyl cis-2-[[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]methyl]pyrrolidine-1-carboxylate was synthesized according to General procedure L from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (±)-tert-butyl 2-(aminomethyl)pyrrolidine-1-carboxylate and was used in step 2 without purification.

Step 2: the title compound was synthesized according to General procedure C from tert-butyl cis-2-[[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]methyl]pyrrolidine-1-carboxylate. LCMS [M+H]⁺ 506. 1H-NMR (400 MHz, Methanol-d4) δ ppm 7.68 (d, J=7.9 Hz, 1H), 7.49 (d, J=7.9 Hz, 1H), 7.23-7.30 (m, 1H), 7.16 (t, J=7.9 Hz, 1H), 7.06-7.12 (m, 1H), 7.02-7.06 (m, 1H), 4.36-4.49 (m, 1H), 3.87 (s, 3H), 3.65-3.85 (m, 3H), 3.27-3.43 (m, 2H), 2.66-2.83 (m, 3H), 2.20-2.33 (m, 3H), 2.17 (s, 3H), 1.99-2.15 (m, 2H), 1.80-1.93 (m, 3H), 1.58-1.74 (m, 2H).

Example 255: Cis-4-[4-(2-aminoacetamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: tert-butyl N-[2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]amino]-2-oxo-ethyl]carbamate was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 2-[(tert-butoxy)carbonyl]aminoacetic acid and was used in step 2 without purification.

Step 2: the title compound was synthesized according to General procedure C from tert-butyl N-[2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]amino]-2-oxo-ethyl]carbamate LCMS [M+H]⁺ 452. ¹H-NMR (400 MHz, Methanol-d4) d ppm 7.43 (d, J=7.9 Hz, 1H), 7.25-7.30 (m, 1H), 7.06-7.12 (m, 2H), 6.99-7.06 (m, 2H), 4.38-4.49 (m, 1H), 3.95 (s, 2H), 3.88 (s, 3H), 2.71-2.84 (m, 3H), 2.23-2.33 (m, 2H), 2.17 (s, 3H), 1.81-1.93 (m, 2H), 1.65-1.76 (m, 2H).

Example 256: Cis-4-[5-(aminomethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

A mixture of 4-(5-cyano-2-oxo-3H-benzimidazol-1-yl)-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide (1.0 equiv.), triethylamine (10 equiv.), and Pd/C (0.25 equiv.) was stirred in THE and formic acid at 40° C. for 48 h. The product was isolated by preparative HPLC. LCMS [M+H]⁺ 409.

Example 257: Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-1,3-benzodiazol-2-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 2-amino-1-methylbenzimidazole. LCMS [M+H]⁺ 468.

Example 258: Methyl 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylate

Step 1: methyl 3-[[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-benzoate was synthesized according to General procedure A from cis-4-amino-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide hydrochloride and methyl 3-fluoro-2-nitro-benzoate. LCMS [M+H]⁺ 442.

Step 2: the title compound was synthesized according to General procedure F from methyl 3-[[cis-4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-benzoate. LCMS [M+H]⁺ 438.

Example 259: N-Methyl-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and methylammonium chloride. LCMS [M+H]⁺ 437.

Example 260: N,N-Dimethyl-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and dimethylammonium chloride. LCMS [M+H]⁺ 451.

Example 261: Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperazine-1-carbonyl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and piperazine. LCMS [M+H]⁺ 492.

Example 262: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(morpholine-4-carbonyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and morpholine. LCMS [M+H]⁺ 493.

Example 263: N-(2-Hydroxyethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and ethanolamine. LCMS [M+H]⁺ 467.

Example 264: Cis-4-{4-[(2-carbamoylethyl)carbamoyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 3-aminopropanamide. LCMS [M+H]⁺ 494.

Example 265: N-(3-Aminopropyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 1,3-diaminopropane. LCMS [M+H]⁺ 480.

Example 266: N-Methyl-N-[2-(methylamino)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and N,N′-dimethylethylenediamine. LCMS [M+H]⁺ 494.

Example 267: Cis-4-{4-[(3R)-3-(dimethylamino)pyrrolidine-1-carbonyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (R)-(+)-3-(dimethylamino)pyrrolidine. LCMS [M+H]⁺ 520.

Example 268: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(4-methylpiperazine-1-carbonyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and N-methylpiperazine. LCMS [M+H]⁺ 506.

Example 269: Cis-4-{4-[4-(dimethylamino)piperidine-1-carbonyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 4-dimethylaminopiperidine. LCMS [M+H]⁺ 534.

Example 270: N-[(1H-Imidazol-2-yl)methyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 1H-imidazol-2-ylmethanamine. LCMS [M+H]⁺ 503.

Example 271: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(2S)-2-[(pyrrolidin-1-yl)methyl]pyrrolidine-1-carbonyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (S)-(+)-1-(2-pyrrolidinylmethyl)pyrrolidine. LCMS [M+H]⁺ 560.

Example 272: N-[2-(Morpholin-4-yl)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 4-(2-aminoethyl)morpholine. LCMS [M+H]⁺ 536.

Example 273: 2-Oxo-N-[(oxolan-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and tetrahydrofuran-2-ylmethanamine. LCMS [M+H]⁺ 507.

Example 274: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[3-(trifluoromethyl)piperazine-1-carbonyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (±)-2-trifluoromethylpiperazine. LCMS [M+H]⁺ 560.

Example 275: Cis-4-(4-{4-[2-(dimethylamino)ethyl]piperazine-1-carbonyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 1-(2-dimethylamino-ethyl)-piperazine. LCMS [M+H]⁺ 563.

Example 276: 2-Oxo-N-[(pyrimidin-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 2-aminomethylpyrimidine hydrochloride. LCMS [M+H]⁺ 515.

Example 277: N-Methyl-N-(1-methylpyrrolidin-3-yl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (±)-N,N′-dimethyl-3-aminopyrrolidine. LCMS [M+H]⁺ 520.

Example 278: 1-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carbonyl}pyrrolidine-2-carboxamide

The title compound was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (±)-2-pyrrolidinecarboxamide hydrochloride. LCMS [M+H]⁺ 520.

Example 279: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(pyrimidin-2-yl)amino]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

Step 1: A mixture of pyrimidine-2-amine (1.0 equiv.) and NaH (1.1 equiv.) was stirred in THE for 10 min, then 1,3-difluoro-2-nitro-benzene (1.0 equiv.) was added and the resulting mixture was stirred for 16 h at 65° C. The reaction mixture was then concentrated and purified by silica gel chromatography which afforded N-(3-fluoro-2-nitro-phenyl)pyrimidin-2-amine. LCMS [M+H]⁺ 235. ¹H-NMR (400 MHz, CHLOROFORM-d) 6 ppm 9.05 (br. s., 1H), 8.53 (d, J=4.7 Hz, 2H), 8.47 (dt, J=8.6, 1.3 Hz, 1H), 7.52 (td, J=8.6, 5.7 Hz, 1H), 6.93 (t, J=4.7 Hz, 1H), 6.88-6.94 (m, 1H).

Step 2: N-(3-methoxy-4-methyl-phenyl)-4-[2-nitro-3-(pyrimidin-2-ylamino)anilino]cyclohexanecarboxamide was synthesized according to general procedure A from N-(3-fluoro-2-nitro-phenyl)pyrimidin-2-amine and cis-4-amino-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide hydrochloride. LCMS [M+H]⁺ 477. ¹H-NMR (400 MHz, CHLOROFORM-d) δ ppm 10.69 (s, 1H), 8.50 (d, J=5.1 Hz, 2H), 8.16-8.39 (m, 1H), 7.82 (d, J=8.5 Hz, 1H), 7.44 (d, J=1.9 Hz, 1H), 7.35 (t, J=8.4 Hz, 1H), 7.18 (s, 1H), 7.04 (d, J=7.9 Hz, 1H), 6.86 (t, J=4.9 Hz, 1H), 6.74 (dd, J=7.9, 1.9 Hz, 1H), 6.50 (d, J=8.5 Hz, 1H), 3.85 (s, 3H), 3.79-3.84 (m, 1H), 2.39-2.48 (m, 1H), 2.17 (s, 3H), 2.00-2.08 (m, 3H), 1.89-1.98 (m, 4H), 1.78-1.87 (m, 2H).

Step 3: The title compound was synthesized according to general procedure F. LCMS [M+H]⁺ 473. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.55 (s, 1H), 9.81 (s, 1H), 9.12 (s, 1H), 8.44 (d, J=5.1 Hz, 2H), 7.44 (dd, J=8.2, 0.6 Hz, 1H), 7.29 (d, J=1.9 Hz, 1H), 7.18 (dd, J=7.9, 1.9 Hz, 1H), 7.09 (d, J=7.9 Hz, 1H), 7.06 (br. d, J=8.0 Hz, 1H), 6.95 (t, J=8.1 Hz, 1H), 6.84 (t, J=4.9 Hz, 1H), 4.22-4.32 (m, 1H), 3.78 (s, 3H), 2.70-2.76 (m, 1H), 2.53-2.65 (m, 2H), 2.11-2.19 (m, 2H), 2.10 (s, 3H), 1.67-1.80 (m, 2H), 1.50-1.60 (m, 2H).

Example 280: Cis-4-(4-{[2-(dimethylamino)ethyl]amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: cis-4-[3-[benzyl-[2-(dimethylamino)ethyl]amino]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to General procedure A from Cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N-benzyl-N′,N′-dimethylethylenediamine.

LCMS [M+H]⁺ 560.

Step 2: cis-4-[4-[benzyl-[2-(dimethylamino)ethyl]amino]-2-oxo-3H-benzimidazol-1-yl]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to General procedure B from 4-[3-[benzyl-[2-(dimethylamino)ethyl]amino]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 556.

Step 3: the title compound was synthesized according to General procedure G from cis-4-[4-[benzyl-[2-(dimethylamino)ethyl]amino]-2-oxo-3H-benzimidazol-1-yl]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 466.

Example 281: tert-Butyl N-(1-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidin-3-yl)carbamate

Step 1: tert-butyl N-[1-[3-cis-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-phenyl]pyrrolidin-3-yl]carbamate was synthesized according to General procedure A from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (±)-tert-butyl N-pyrrolidin-3-ylcarbamate. LCMS [M+H]⁺ 568.

Step 2: The title compound was synthesized according to General procedure B from tert-butyl N-[1-[3-cis-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-phenyl]pyrrolidin-3-yl]carbamate. LCMS [M+H]⁺ 564.

Example 282: Cis-4-[4-(3-aminopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure C from tert-butyl N-(1-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidin-3-yl)carbamate. LCMS [M+H]⁺ 464.

Example 283: Cis-4-{4-[2-(dimethylamino)acetamido]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N,N-dimethylglycine. LCMS [M+H]⁺ 480.

Example 284: Cis-4-[4-(3-aminopropanamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: tert-Butyl N-[3-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]amino]-3-oxo-propyl]carbamate was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and N-(tert-butoxycarbonyl)-β-alanine and was used in step 2 without purification.

Step 2 The title compound was synthesized according to General procedure C from tert-butyl N-[3-[[i-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]amino]-3-oxo-propyl]carbamate. LCMS [M+H]⁺ 466.

Example 285: Cis-N-(3-methoxy-4-methylphenyl)-4-{4-[2-(morpholin-4-yl)acetamido]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and morpholin-4-yl-acetic acid hydrochloride.

LCMS [M+H]⁺ 522.

Example 286: (2S,4R)-4-Hydroxy-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidine-2-carboxamide

Step 1: tert-Butyl (2S,4R)-4-hydroxy-2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]carbamoyl]pyrrolidine-1-carboxylate was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (2S,4R)-1-(tert-Butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure C from tert-butyl (2S,4R)-4-hydroxy-2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]carbamoyl]pyrrolidine-1-carboxylate. LCMS [M+H]⁺ 508.

Example 287: (2S)—N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}azetidine-2-carboxamide

Step 1: tert-butyl (2S)-2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]carbamoyl]azetidine-1-carboxylate was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (2S)-1-tert-butoxycarbonylazetidine-2-carboxylic acid and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure C from tert-butyl (2S)-2-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]carbamoyl]azetidine-1-carboxylate. LCMS [M+H]⁺ 478.

Example 288: Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

A mixture of cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), acetic anhydride (1.0 equiv.), and diisopropylethylamine (2.0 equiv.) was stirred in THE at 20° C. for 16 h. The crude reaction mixture was then purified by preparative HPLC followed by recrystallization from EtOH/water. LCMS [M+H]⁺ 437.

Example 289: N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}morpholine-2-carboxamide

Step 1: 4-benzyl-N-[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]morpholine-2-carboxamide was synthesized according to General procedure H from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 4-benzyl-2-morpholinecarboxylic acid hydrochloride and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure G from 4-benzyl-N-[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]morpholine-2-carboxamide. LCMS [M+H]⁺ 508.

Example 290: Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure H from cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 1H-indol-6-amine. LCMS [M+H]⁺ 432. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.01 (s, 1H), 10.38 (s, 1H), 9.77 (s, 1H), 9.52 (s, 1H), 8.00-8.03 (m, 1H), 7.44 (d, J=8.2 Hz, 1H), 7.26 (dd, J=3.0, 2.4 Hz, 1H), 7.16 (d, J=7.9 Hz, 1H), 7.04-7.10 (m, 2H), 6.93-6.98 (m, 1H), 6.35 (ddd, J=3.1, 2.0, 0.9 Hz, 1H), 4.21-4.33 (m, 1H), 2.71-2.80 (m, 1H), 2.57-2.70 (m, 2H), 2.10-2.21 (m, 2H), 2.05 (s, 3H), 1.68-1.80 (m, 2H), 1.50-1.60 (m, 2H).

Example 291: 2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: cis-1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-N-[(4-methoxyphenyl)methyl]-2-oxo-3H-benzimidazole-4-carboxamide was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and 4-methoxybenzylamine and was used in step 2 without purification.

Step 2: A mixture of 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide and TFA was stirred at 70° C. for 16 h. The excess TFA was then evaporated and the crude material was purified by preparative HPLC which afforded the title compound. LCMS [M+H]⁺ 423.

Example 292: N-[(Morpholin-3-yl)methyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: tert-butyl 3-[[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]methyl]morpholine-4-carboxylate was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (±) tert-butyl 3-(aminomethyl)morpholine-4-carboxylate and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure C from the crude tert-butyl 3-[[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]methyl]morpholine-4-carboxylate from step 1. LCMS [M+H]⁺ 522.

Example 293: N-(Azetidin-3-yl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: tert-butyl 3-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]azetidine-1-carboxylate was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and tert-butyl 3-aminoazetidine-1-carboxylate and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure C from the crude tert-butyl 3-[[-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]azetidine-1-carboxylate from step 1. LCMS [M+H]⁺ 478.

Example 294: 2-Oxo-N-(pyrrolidin-3-yl)-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide

Step 1: tert-butyl 3-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]pyrrolidine-1-carboxylate was synthesized according to General procedure H from 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylic acid and (±) tert-butyl 3-aminopyrrolidine-1-carboxylate and was used in step 2 without purification.

Step 2: The title compound was synthesized according to General procedure C from the crude tert-butyl 3-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazole-4-carbonyl]amino]pyrrolidine-1-carboxylate from step 1. LCMS [M+H]⁺ 492.

Example 295: Cis-4-{4-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: cis-4-[3-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and S-3-(dimethylamino)pyrrolidine. LCMS [M+H]⁺ 496. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.44 (s, 1H), 7.38 (s, 1H), 7.15 (t, J=8.4 Hz, 1H), 7.03 (d, J=8.2 Hz, 1H), 6.95 (d, J=7.0 Hz, 1H), 6.78 (dd, J=8.1, 1.7 Hz, 1H), 6.16 (d, J=8.2 Hz, 1H), 6.08 (d, J=8.5 Hz, 1H), 3.84 (s, 3H), 3.71 (br. s., 1H), 3.45-3.54 (m, 1H), 3.28-3.42 (m, 2H), 3.15-3.24 (m, 2H), 2.52 (s, 6H), 2.37-2.47 (m, 1H), 2.25 (d, J=4.7 Hz, 1H), 2.16 (s, 3H), 2.07-2.15 (m, 1H), 1.69-2.04 (m, 8H).

Step 2: The title compound was synthesized according to General procedure F from cis-4-[3-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 492.

Example 296: Cis-N-(3-Methoxy-4-methylphenyl)-4-{4-[methyl(1-methylpyrrolidin-3-yl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

Step 1: N-(3-methoxy-4-methyl-phenyl)-4-[3-[methyl-(1-methylpyrrolidin-3-yl)amino]-2-nitro-anilino]cyclohexanecarboxamide was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and (±)-N,N′-dimethyl-3-aminopyrrolidine. LCMS [M+H]⁺ 496. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.44 (d, J=1.6 Hz, 1H), 7.39 (s, 1H), 7.24 (t, J=8.2 Hz, 1H), 7.03 (d, J=8.2 Hz, 1H), 6.76 (dd, J=7.9, 1.9 Hz, 1H), 6.52 (d, J=8.5 Hz, 1H), 6.44 (d, J=7.9 Hz, 1H), 5.44-5.62 (m, 1H), 3.94-4.01 (m, 1H), 3.82-3.86 (m, 3H), 3.60-3.70 (m, 1H), 3.40-3.52 (m, 1H), 3.22-3.34 (m, 1H), 3.00-3.10 (m, 1H), 2.90 (br. s., 1H), 2.73 (s, 3H), 2.69 (s, 3H), 2.40-2.48 (m, 1H), 2.18-2.29 (m, 1H), 2.17 (s, 3H), 1.73-1.98 (m, 9H).

Step 2: the title compound was synthesized according to General procedure F from N-(3-methoxy-4-methyl-phenyl)-4-[3-[methyl-(1-methylpyrrolidin-3-yl)amino]-2-nitro-anilino]cyclohexanecarboxamide. LCMS [M+H]⁺ 492. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.79 (s, 1H), 9.88 (s, 1H), 7.37 (d, J=1.6 Hz, 1H), 7.26 (dd, J=8.1, 1.7 Hz, 1H), 7.14 (d, J=8.2 Hz, 1H), 7.07 (d, J=7.9 Hz, 1H), 6.97 (t, J=7.9 Hz, 1H), 6.74 (d, J=7.9 Hz, 1H), 4.28-4.39 (m, 1H), 3.90-3.98 (m, 1H), 3.87 (s, 3H), 2.78-2.84 (m, 1H), 2.68 (s, 3H), 2.60-2.67 (m, 4H), 2.52-2.57 (m, 1H), 2.37-2.46 (m, 1H), 2.29 (s, 3H), 2.20-2.26 (m, 2H), 2.19 (s, 3H), 1.98-2.09 (m, 1H), 1.73-1.87 (m, 3H), 1.57-1.68 (m, 2H).

Example 297: Cis-N-(3-methoxy-4-methylphenyl)-4-(4-{methyl[2-(methylamino)ethyl]amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

Step 1: tert-butyl N-[2-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]ethyl]-N-methyl-carbamate was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl N-methyl-N-[2-(methylamino)ethyl]carbamate. LCMS [M+H]⁺ 570.

Step 2: tert-butyl N-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]ethyl]-N-methyl-carbamate was synthesized according to General procedure F from tert-butyl N-[2-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]ethyl]-N-methyl-carbamate.

LCMS [M+H]⁺ 566.

Step 3: the title compound was synthesized according to General procedure C from tert-butyl N-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]ethyl]-N-methyl-carbamate. LCMS [M+H]⁺ 466.

Example 298: Cis-4-{4-[(2-aminoethyl)(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: tert-butyl N-[2-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]ethyl]carbamate was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl N-[2-(methylamino)ethyl]carbamate. LCMS [M+H]⁺ 556. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 7.45 (s, 1H), 7.40 (s, 1H), 7.16 (t, J=8.2 Hz, 1H), 7.03 (d, J=7.9 Hz, 1H), 6.77 (d, J=7.9 Hz, 1H), 6.49-6.73 (m, 1H), 6.36 (d, J=8.2 Hz, 1H), 6.29 (d, J=8.2 Hz, 1H), 5.07-5.23 (m, 1H), 3.84 (s, 3H), 3.69 (br. s., 1H), 3.33 (br. s., 4H), 2.80 (s, 3H), 2.37-2.46 (m, 1H), 2.16 (s, 3H), 1.83-2.00 (m, 6H), 1.70-1.81 (m, 2H), 1.39-1.44 (m, 9H).

Step 2: tert-butyl N-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]ethyl]carbamate was synthesized according to General procedure F from tert-butyl N-[2-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]ethyl]carbamate. LCMS [M+H]⁺ 552. ¹H-NMR (400 MHz, Chloroform-d) δ ppm 9.50 (br. s, 1H), 7.36 (br. s., 2H), 7.09 (d, J=8.2 Hz, 2H), 6.93-7.01 (m, 1H), 6.88 (d, J=6.6 Hz, 1H), 6.64-6.75 (m, 1H), 5.22-5.40 (m, 1H), 4.40-4.52 (m, 1H), 3.88 (s, 3H), 3.39 (br. s., 2H), 3.12 (br. s., 2H), 2.78 (br. s., 3H), 2.61-2.73 (m, 3H), 2.25-2.35 (m, 2H), 2.20 (s, 3H), 1.69-1.89 (m, 5H), 1.44 (s, 9H).

Step 3: the title compound was synthesized according to General procedure C from tert-butyl N-[2-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]ethyl]carbamate. LCMS [M+H]⁺ 452. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 9.84 (s, 1H), 7.29 (d, J=1.9 Hz, 1H), 7.18 (dd, J=7.9, 1.9 Hz, 1H), 7.04-7.09 (m, 2H), 6.96 (t, J=7.9 Hz, 1H), 6.76 (d, J=7.6 Hz, 1H), 4.21-4.31 (m, 1H), 3.79 (s, 3H), 3.11-3.17 (m, 2H), 2.98-3.04 (m, 2H), 2.74 (br. s., 1H), 2.63 (s, 3 H), 2.53-2.60 (m, 2H), 2.15 (d, J=13.3 Hz, 2H), 2.10 (s, 3H), 1.67-1.79 (m, 2H), 1.49-1.58 (m, 2H).

Example 299: N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-pyrazole-3-carboxamide

The title compound was synthesized according to General procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1H-pyrazole-3-carboxylic acid. LCMS [M+H]⁺ 489.

Example 300: 5-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,2-oxazole-3-carboxamide

The title compound was synthesized according to General procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 5-methylisoxazole-3-carboxylic acid.

LCMS [M+H]⁺ 504.

Example 301: N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,3-oxazole-5-carboxamide

The title compound was synthesized according to General procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and oxazole-5-carboxylic acid. LCMS [M+H]⁺ 490.

Example 302: Cis-4-{4-[(3-aminopropyl)(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure C from tert-butyl N-[3-[[1-cis-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]propyl]carbamate. LCMS [M+H]⁺ 466. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.77 (s, 1H), 9.83 (s, 1H), 7.61 (br. s., 2H), 7.28 (d, J=1.9 Hz, 1H), 7.18 (dd, J=7.9, 1.9 Hz, 1H), 7.05-7.08 (m, 1H), 7.03 (d, J=7.9 Hz, 1H), 6.94 (t, J=8.1 Hz, 1H), 6.70 (d, J=8.2 Hz, 1H), 4.21-4.32 (m, 1H), 3.79 (s, 3H), 3.07 (br. t, J=7.0, 7.0 Hz, 2H), 2.80-2.88 (m, 2H), 2.71-2.76 (m, 1H), 2.65 (s, 3H), 2.52-2.63 (m, 2H), 2.11-2.18 (m, 2H), 2.11 (s, 3H), 1.67-1.78 (m, 4H), 1.49-1.57 (m, 2H).

Example 303: Cis-4-[4-(4-aminopiperidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: tert-butyl N-[1-[3-cis-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-phenyl]-4-piperidyl]carbamate was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl N-(4-piperidyl)carbamate. LCMS [M+H]⁺ 582.

Step 2: tert-butyl N-[1-cis-[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-4-piperidyl]carbamate was synthesized according to General procedure F from tert-butyl N-[1-[3-cis-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-2-nitro-phenyl]-4-piperidyl]carbamate. LCMS [M+H]⁺ 578.

Step 3: the title compound was synthesized according to General procedure C from tert-butyl N-[1-cis-[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-4-piperidyl]carbamate. LCMS [M+H]⁺ 478. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.86 (s, 1H), 9.81 (s, 1H), 7.91 (br. d, J=4.4 Hz, 3H), 7.28 (d, J=1.9 Hz, 1H), 7.17 (dd, J=7.9, 1.9 Hz, 1H), 7.00-7.07 (m, 2H), 6.92 (t, J=8.1 Hz, 1H), 6.63 (d, J=7.9 Hz, 1H), 4.21-4.31 (m, 1H), 3.78 (s, 3H), 3.24-3.32 (m, 2H), 3.06-3.18 (m, 1H), 2.70-2.75 (m, 1H), 2.52-2.69 (m, 4H), 2.11-2.18 (m, 2H), 2.09 (s, 3H), 1.89-1.97 (m, 2H), 1.66-1.86 (m, 4H), 1.48-1.56 (m, 2H).

Example 304: Cis-4-{4-[2-(dimethylamino)ethoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: cis-4-((3-(2-(dimethylamino)ethoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide was synthesized according to General procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 2-dimethylaminoethanol. LCMS [M+H]⁺ 471.

Step 2: the title compound was synthesized from cis-4-((3-(2-(dimethylamino)ethoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide according to General procedure B. LCMS [M+H]⁺ 467.

Example 305: tert-Butyl N-{3-[methyl({2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl})amino]propyl}carbamate

Step 1: tert-butyl N-[3-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]propyl]carbamate was synthesized according to General procedure M from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl N-[3-(methylamino)propyl]carbamate. LCMS [M+H]⁺ 570.

Step 2: tert-butyl N-[3-[[1-[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]-2-oxo-3H-benzimidazol-4-yl]-methyl-amino]propyl]carbamate was synthesized according to General procedure F from tert-butyl N-[3-[3-[[4-[(3-methoxy-4-methyl-phenyl)carbamoyl]cyclohexyl]amino]-N-methyl-2-nitro-anilino]propyl]carbamate. LCMS [M+H]⁺ 566.

Example 306: Cis-4-{4-[3-(dimethylamino)propoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: cis-4-((3-(3-(dimethylamino)propoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide was synthesized according to General procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 3-dimethylamino-1-propanol. LCMS [M+H]⁺ 485.

Step 2: The title compound was synthesized from cis-4-((3-(3-(dimethylamino)propoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide according to General procedure B. LCMS [M+H]⁺ 481.

Example 307: Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperidin-4-yloxy)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: tert-butyl 4-(3-((cis-4-((3-methoxy-4-methylphenyl)carbamoyl)cyclohexyl)amino)-2-nitrophenoxy)piperidine-1-carboxylate was synthesized according to General procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl 4-hydroxypiperidine-1-carboxylate.

Step 2: the title compound was synthesized from tert-butyl 4-(3-((cis-4-((3-methoxy-4-methylphenyl)carbamoyl)cyclohexyl)amino)-2-nitrophenoxy)piperidine-1-carboxylate according to General procedure B followed by General procedure C. LCMS [M+H]⁺ 479.

Example 308: tert-Butyl N-methyl-N-[2-({2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}oxy)ethyl]carbamate

Step 1: tert-butyl (2-(3-((cis-4-((3-methoxy-4-methylphenyl)carbamoyl)cyclohexyl)amino)-2-nitrophenoxy)ethyl)(methyl)carbamate was synthesized according to General procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and tert-butyl (2-hydroxyethyl)(methyl)carbamate. LCMS [M+H]⁺ 557.

Step 2: the title compound was synthesized from tert-butyl (2-(3-((cis-4-((3-methoxy-4-methylphenyl)carbamoyl)cyclohexyl)amino)-2-nitrophenoxy)ethyl)(methyl)carbamate according to General procedure B. LCMS [M+H]⁺ 553.

Example 309: Cis-N-(3-methoxy-4-methylphenyl)-4-{4-[2-(methylamino)ethoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

The title compound was synthesized according to General procedure C from tert-butyl N-methyl-N-[2-({2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}oxy)ethyl]carbamate. LCMS [M+H]⁺ 453.

Example 310: Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(pyrrolidin-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: cis-N-(3-methoxy-4-methylphenyl)-4-((2-nitro-3-(pyrrolidin-1-yl)phenyl)amino)cyclohexanecarboxamide was synthesized from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and pyrrolidine according to General procedure M. LCMS [M+H]⁺ 453.

Step 2: the title compound was synthesized from cis-N-(3-methoxy-4-methylphenyl)-4-((2-nitro-3-(pyrrolidin-1-yl)phenyl)amino)cyclohexanecarboxamide according to General procedure B. LCMS [M+H]⁺ 449.

Example 311: Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(1,2,3,6-tetrahydropyridin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: A mixture of cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate (1.3 equiv.), Pd(dba)₂ (0.10 equiv.), S-Phos (0.10 equiv.), and triethylamine (5.3 equiv.) were dissolved in ethanol. The vial was flushed with nitrogen and sealed, thereafter the resulting reaction mixture was stirred at 120° C. for 24 h. After cooling, the reaction mixture was filtered through a short plug of silica. The material was concentrated and used in the next step without further purification.

Step 2: the filtrate from step 1 was dissolved in DCM, then trifluoroacetic acid was added. After complete reaction the mixture was purified by preparative HPLC which afforded the title compound.

LCMS [M+H]⁺ 461.

Example 312: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

A mixture of cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate (1.3 equiv.), Pd(dba)₂ (0.10 equiv.), S-Phos (0.10 equiv.), and triethylamine (5.3 equiv.) were dissolved in ethanol. The vial was flushed with nitrogen and sealed and the resulting reaction mixture was stirred at 120° C. for 24 h. After cooling, the material was concentrated and purified by preparative HPLC which afforded the title compound. LCMS [M+H]⁺ 475.

Example 313: Cis-4-[4-(3-acetamidopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

A mixture of cis-4-[4-(3-aminopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide, diisopropylethylamine, and acetic anhydride was stirred DCM for 16 h. The mixture was concentrated and purified by preparative HPLC which afforded the title compound. LCMS [M+H]⁺ 506.

Example 314: Cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide

Step 1: 4-[3-(4,6-dihydro-1H-pyrrolo[3,4-c]pyrazol-5-yl)-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide was synthesized according to General procedure A from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole dihydrochloride. LCMS [M+H]⁺ 491.

Step 2: The title compound was synthesized according to General procedure B from 4-[3-(4,6-dihydro-1H-pyrrolo[3,4-c]pyrazol-5-yl)-2-nitro-anilino]-N-(3-methoxy-4-methyl-phenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 487.

Example 315: Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indazol-5-yl)cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure H from cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxylic acid and 1H-indazol-5-amine. LCMS [M+H]⁺ 433. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.39 (s, 1H), 9.89 (s, 1H), 9.53 (s, 1H), 8.18 (dd, J=1.7, 0.8 Hz, 1H), 8.06 (d, J=0.6 Hz, 1H), 7.49-7.52 (m, 1H), 7.46 (dd, J=9.0, 2.0 Hz, 1H), 7.16 (d, J=7.9 Hz, 1H), 7.08 (d, J=7.6 Hz, 1H), 6.94-7.00 (m, 1H), 4.23-4.34 (m, 1H), 2.73-2.82 (m, 1H), 2.57-2.70 (m, 2H), 2.12-2.22 (m, 2H), 2.06 (s, 3H), 1.71-1.81 (m, 2H), 1.57 (d, J=9.8 Hz, 2H).

Example 316: Methyl N-(1-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidin-3-yl)carbamate

A mixture of cis-4-[4-(3-aminopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide (1.0 equiv.), N,N-diisopropylethylamine (2.0 equiv.), and methyl chloroformate (1.0 equiv.) was stirred in DCM at 20° C. for 3 h. The mixture was then purified by silica gel chromatography which afforded the title compound. LCMS [M+H]⁺ 522.

Example 317: Cis-4-{4-[3-(2-hydroxy-2-methylpropanamido)pyrrolidin-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

The title compound was synthesized according to general procedure O from cis-4-[4-(3-aminopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and α-hydroxyisobutyric acid. LCMS [M+H]⁺ 550. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.46 (s, 1H), 9.79 (s, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.28 (d, J=1.9 Hz, 1H), 7.16 (dd, J=7.9, 1.9 Hz, 1H), 7.03-7.07 (m, 1H), 6.84-6.88 (m, 2H), 6.36-6.41 (m, 1H), 4.20-4.36 (m, 2H), 3.35-3.45 (m, 2H), 3.16-3.26 (m, 2H), 2.70-2.74 (m, 1H), 2.52-2.63 (m, 2H), 2.14 (d, J=14.5 Hz, 3H), 2.09 (s, 3H), 1.77-1.86 (m, 1H), 1.66-1.77 (m, 2H), 1.48-1.56 (m, 2H), 1.24 (d, J=4.4 Hz, 6H).

Example 318: 1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-imidazole-2-carboxamide

The title compound was synthesized according to general procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1-methylimidazole-2-carboxylic acid.

LCMS [M+H]⁺ 503.

Example 319: 1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-imidazole-4-carboxamide

The title compound was synthesized according to general procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1-methylimidazole-4-carboxylic acid.

LCMS [M+H]⁺ 503. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.73 (s, 1H), 9.90 (s, 1H), 9.82 (s, 1H), 8.20-8.31 (m, 1H), 7.97 (s, 1H), 7.30 (d, J=1.9 Hz, 1H), 7.22 (d, J=7.9 Hz, 1H), 7.15-7.19 (m, 2H), 7.03-7.07 (m, 1H), 6.99 (t, J=8.1 Hz, 1H), 4.22-4.33 (m, 1H), 3.81 (s, 3H), 3.79 (s, 3H), 2.71-2.76 (m, 1H), 2.53-2.66 (m, 3H), 2.11-2.19 (m, 3H), 2.10 (s, 3H), 1.68-1.80 (m, 2H), 1.52-1.60 (m, 2H).

Example 320: 2-Amino-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,3-oxazole-4-carboxamide

The title compound was synthesized according to general procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1-methylimidazole-4-carboxylic acid.

LCMS [M+H]⁺ 505.

Example 321: 1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-pyrazole-5-carboxamide

The title compound was synthesized according to general procedure O from cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 1-methylimidazole-4-carboxylic acid.

LCMS [M+H]⁺ 503. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 10.65-10.70 (m, 1H), 9.99 (s, 1H), 9.79-9.84 (m, 1H), 7.53 (d, J=1.9 Hz, 1H), 7.31 (d, J=2.0 Hz, 1H), 7.22 (br. d, J=7.4 Hz, 1H), 7.17 (dd, J=8.2, 1.9 Hz, 1H), 7.03-7.08 (m, 4H), 7.00 (t, J=7.8 Hz, 1H), 4.23-4.33 (m, 1H), 4.09 (s, 3H), 3.79 (s, 3H), 2.70-2.77 (m, 1H), 2.53-2.66 (m, 2H), 2.12-2.19 (m, 3H), 2.10 (s, 3H), 1.68-1.80 (m, 2H), 1.52-1.61 (m, 2H).

Example 322: Cis-N-(4-fluorophenyl)-4-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarboxamide

Step 1: cis-4-((2-nitrophenyl)amino)cyclohexanecarboxylic acid was synthesized according to general procedure A. LCMS [M+H]⁺ 265.

Step 2: cis-4-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarboxylic acid synthesized according to general procedure B from cis-4-((2-nitrophenyl)amino)cyclohexanecarboxylic acid and diphosgene. LCMS [M+H]⁺ 261.

Step 3: The title compound was synthesized according to general procedure O from cis-4-(2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarboxylic acid. LCMS [M+H]⁺ 354.

Example 323: Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(2,2,2-trifluoroethyl)amino]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide

Step 1: 3-fluoro-2-nitro-N-(2,2,2-trifluoroethyl)aniline was synthesized according to general procedure A from 2,2,2-trifluoroethanamine hydrochloride and 1,3-difluoro-2-nitrobenzene. LCMS [M+H]⁺ 239.

Step 2: cis-N-(3-methoxy-4-methyl-phenyl)-4-[2-nitro-3-(2,2,2-trifluoroethylamino)anilino]cyclohexanecarboxamide was synthesized according to general procedure A from cis-4-amino-N-(3-methoxy-4-methyl-phenyl)-cyclohexanecarboxamide hydrochloride and 3-fluoro-2-nitro-N-(2,2,2-trifluoroethyl)aniline. LCMS [M+H]⁺ 481.

Step 3: The title compound was synthesized according to general procedure F. LCMS [M+H]⁺ 477.

Example 324: Cis-4-{4-[(2,2-difluoroethyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide

Step 1: N-(2,2-difluoroethyl)-3-fluoro-2-nitro-aniline was synthesized according to general procedure A from 2,2-difluoroethanamine and 1,3-difluoro-2-nitrobenzene. LCMS [M+H]⁺ 221.

Step 2: N-(3-methoxy-4-methyl-phenyl)-cis-4-[2-nitro-3-(2,2,2-trifluoroethylamino)anilino]cyclohexanecarboxamide was synthesized according to general procedure A from N-(2,2-difluoroethyl)-3-fluoro-2-nitro-aniline and cis-4-amino-N-(3-methoxy-4-methyl-phenyl)-cyclohexanecarboxamide hydrochloride. LCMS [M+H]⁺ 463.

Step 3: The title compound was synthesized according to general procedure F from N-(3-methoxy-4-methyl-phenyl)-cis-4-[2-nitro-3-(2,2,2-trifluoroethylamino)anilino]cyclohexanecarboxamide. LCMS [M+H]⁺ 459.

Example 325: Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(3-methylbutoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide

Step 1: cis-4-((3-(isopentyloxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide was synthesized according to general procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 3-methylbutan-1-ol. LCMS [M+H]⁺ 470.

Step 2: The title compound was according to General procedure B from cis-4-((3-(isopentyloxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 466.

Example 326: Cis-4-(4-(2-(cyclohexyloxy)ethoxy)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide

Step 1: cis-4-((3-(2-(cyclohexyloxy)ethoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide was synthesized according to general procedure N from cis-4-[(3-fluoro-2-nitrophenyl)amino]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide and 2-(cyclohexyloxy)ethanol. LCMS [M+H]⁺ 526.

Step 2: The title compound was synthesized according to General procedure B from cis-4-((3-(2-(cyclohexyloxy)ethoxy)-2-nitrophenyl)amino)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide. LCMS [M+H]⁺ 522.

The chemical names of the compounds described herein have been generated using as software Marvin Sketch version 18.22.3 and ACD Labs ChemSketch version 12.0.

For the avoidance of doubt, it is pointed out that in the event of a discrepancy between the chemical name and the structural formula of any particular compound, the structural formula prevails, unless contradicted by any experimental details or unless otherwise is clear from the context. The structural formulas of the Examples are shown in Table 1.

TABLE 1
Example Structural formula
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326

BIOLOGICAL EXAMPLES

The biological activity of example compounds as described herein above was assessed using the following biological assays.

Biological Example 1: OGG1 Inhibition

Method 1: In Vitro OGG1 Activity Assay

OGG1 activity is assayed by measuring the increase in fluorescence from a duplex oligonucleotide containing an OGG1 substrate and a fluorophore in close proximity that are quenched by a quencher on the complementary strand. One single-stranded DNA oligonucleotide with the sequence 5′-FAM-TCTG CCA 8CA CTG CGT CGA CCT G-3′ (SEQ ID NO 1) is annealed to a 25% surplus of 5′-CAG GTC GAC GCA GTG CTG GCA GT-Dab-3′ (SEQ ID NO 2), where “8” signifies 8-oxo-2′deoxyadenosine and “FAM” and “Dab” signify fluorescein and dabcyl, respectively. OGG1 activity releases the substrate base from DNA by cleaving the N-glycosidic bond between base and deoxyribose. The resulting apurinic site is cleaved by an excessive amount APEX1 activity which cause the duplex to melt, which in turn cause the fluorophore to become unquenched. Compounds to be tested are dissolved in DMSO and nano-dispensed directly into black 384-well plates, followed by transfer of enzyme and substrate solutions. Enzyme and DNA substrate solutions are added so that the assay mixture contains final concentrations of 25 mM Tris-HCl pH 8.0, 15 mM NaCl, 2 mM MgCl₂, 0.5 mM DTT and 0.0025% Tween-20, 800 pM OGG1 enzyme, 2 nM human APEX1 and 10 nM 8-oxoA:C substrate. The fluorescent signal is recorded in a plate reader equipped with suitable filters to register fluorescein fluorescence. The IC50 value is determined by fitting a dose response curve to the data points using nonlinear regression analysis and the equation Y=Bottom+(Top−Bottom)/(1+10{circumflex over ( )}((Log IC50−X)*HillSlope)), where Y is the fluorescein signal read at 530 nm and X is log [compound]. Results obtained for the example compounds described herein are provided in Table 2.

TABLE 2
Example IC50 (nM)
1       2796
2       1691
3       1293
4       660
5       1458
6       540
7       1084
8       1547
9       796
10      3956
11      1775
12      2354
13      359
14      6157
15      1912
16      3876
17      1423
18      1390
19      1870
20      1310
21      3070
22      848
23      728
24      1040
25      765
26      1020
27      488
28      766
29      2060
30      1710
31      1090
32      1190
33      2530
34      502
35      1970
36      3650
37      1590
38      1210
39      788
40      6320
41      1730
42      2410
43      2460
44      3140
45      5030
46      603
47      3800
48      551
49      379
50      149
51      2830
52      1340
53      2050
54      3120
55      4560
56      2120
57      3130
58      3870
59      3290
60      506
61      1865
62      1730
63      1860
64      2350
65      892
66      4510
67      4610
68      1210
69      3880
70      1330
71      9060
72      67
73      4360
74      803
75      223
76      5380
77      358
78      840
79      1900
80      4320
81      408
82      1000
83      958
84      30
85      33
86      59
87      471
88      1760
89      90
90      218
91      58
92      84
93      91
94      105
95      1808
96      1874
97      1725
98      2621
99      1165
100     1187
101     2264
102     2767
103     1455
104     2281
105     2940
106     1753
107     23
108     2531
109     6460
110     4360
111     5810
112     4940
113     3200
114     690
115     1430
116     2060
117     1360
118     234
119     72
120     1910
121     186
122     71
123     26
124     65
125     3620
126     12
127     1220
128     1310
129     116
130     551
131     676
132     6830
133     865
134     2740
135     94
136     501
137     2030
138     2010
139     58
140     25
141     5480
142     497
143     1200
144     983
145     1080
146     27
147     36
148     98
149     86
150     106
151     526
152     74
153     383
154     383
155     1820
156     173
157     152
158     6050
159     4940
160     81
161     175
162     1290
163     3160
164     43
165     1390
166     41
167     3890
168     44
169     9090
170     8800
171     211
172     7790
173     2420
174     2540
175     2620
176     1080
177     5020
178     6920
179     1570
180     8890
181     7090
182     4790
183     174
184     325
185     1390
186     2030
187     338
188     4630
189     1760
190     467
191     55.7
192     34.2
193     1380
194     17.2
195     3560
196     647
197     38.9
198     5370
199     494
200     631
201     35.1
202     52.8
203     6270
204     65.6
205     74.5
206     15.4
207     73.6
208     115
209     402
210     9490
211     153
212     9.43
213     155
214     556
215     580
216     8130
217     586
218     9010
219     2440
220     8630
221     27.2
222     350
223     1670
224     3660
225     33.5
226     77.9
227     17.9
228     0.15
229     29.8
230     606
231     8050
232     109
233     47.6
234     572
235     1450
236     196
237     67.1
238     40.9
239     50.6
240     15.3
241     960
242     126
243     1470
244     60.7
245     2760
246     3630
247     0.62
248     6.77
249     21.9
250     23.5
251     4.25
252     3.94
253     6.79
254     0.21
255     30.9
256     2690
257     26.9
258     5.83
259     3.94
260     343
261     68.3
262     348
263     2.71
264     5.77
265     0.28
266     8.16
267     82.4
268     152.73
269     139.97
270     0.39
271     56
272     4.11
273     17.51
274     92.14
275     170.85
276     2.9
277     48.24
278     221.41
279     74.5
280     27.5
281     149
282     10.1
283     14
284     1.73
285     45.1
286     18.1
287     27.1
288     23
289     51.7
290     239
291     9.53
292     0.37
293     1.42
294     1.21
295     9.62
296     28.6
297     8.07
298     12.02
299     27.2
300     9.9
301     6.91
302     16.4
303     10.6
304     3.8
305     251
306     2.82
307     12.5
308     157
309     3.26
310     51.6
311     4.49
312     2.94
313     21.3
314     56.33
315     759
316     38
317     39.1
318     79.5
319     20.3
320     21.97
321     5.75
322     2627
323     226.4
324     96.9
325     314
326     118

Biological Example 2: Cell Viability, Proliferation and Survival Assays

Method 2: Generation of OGG1 Knockdown Cell Line

The H460 and A3 cancer cell lines were stably transfected with a containing non-targeting shRNA hairpins or shRNA hairpins targeting OGG1. The following sequences were used to insert the hairpins into the BshTI and EcoRI site of the pRSITEP-U6Tet-(sh)-EF1-TetRep-P2A-Puro-P2A-RFP670 plasmid:

Non-targeting-f:
(SEQ ID NO 3)
CCG GCC TAA GGT TAA GTC GCC CTC GCT CGA GCG AGG
GCG ACT TAA CCT TAA GGT TTT TG,
Non-targeting-r:
(SEQ ID NO 4)
AAT TCA AAA ACC TAA GGT TAA GTC GCC CTC GCT CGA
GCG AGG GCG ACT TAA CCT TAG G,
shOGG1#1-f:
(SEQ ID NO 5)
CCG GTG GAG TGG TGT ACT AGC GGA TCT CGA GAT CCG
CTA GTA CAC CAC TCC ATT TT TG,
shOGG1#1-r:
(SEQ ID NO 6)
AAT TCA AAA ATG GAG TGG TGT ACT AGC GGA TCT CGA
GAT CCG CTA GTA CAC CAC TCC A,
shOGG1#2-f:
(SEQ ID NO 7)
CCG GGT GTG CGA CTG CTG CGA CAA GCT CGA GCT TGT
CGC AGC AGT CGC ACA CTT TTT G,
shOGG1#2-r:
(SEQ ID NO 8)
AAT TCA AAA AGT GTG CGA CTG CTG CGA CAA GCT CGA
GCT TGT CGC AGC AGT CGC ACA C,
shOGG1#3-f:
(SEQ ID NO 9)
CCG GTG TGC CCG TGG ATG TCC ATA TCT CGA GAT ATG
GAC ATC CAC GGG CAC ATT TTT G,
shOGG1#3-r:
(SEQ ID NO 10)
AAT TCA AAA ATG TGC CCG TGG ATG TCC ATA TCT CGA
GAT ATG GAC ATC CAC GGG CAC A.

The plasmids were packaged in lentiviral particles and transduced into A3 cells and selected with 1 μg/ml puromycin for 6 days, followed by fluorescence activated cell sorting of the top 15% of the RFP670-positive cell population.

The following sequence was inserted into the SalI and NotI cloning sites of pENTR1A plasmid and shuttled into pLenti PGK Hygro DEST (w530-1) expression vector.

(SEQ ID NO 11)
1    ATGCCCGCAA GAGCTCTCTT GCCAAGGCGA ATGGGTCATC GAACACTTGC
51   AAGTACCCCG GCCCTGTGGG CATCTATACC TTGCCCACGG TCCGAACTGC
101  GACTGGACCT TGTGTTGCCC AGCGGCCAGA GCTTTAGATG GCGGGAACAA
151  AGCCCCGCAC ATTGGTCAGG AGTCTTGGCA GACCAGGTAT GGACTCTCAC
201  GCAAACTGAG GAGCAGCTCC ATTGCACCGT GTATAGAGGA GATAAGAGTC
251  AAGCCAGCAG GCCCACGCCT GACGAATTGG AAGCAGTCAG AAAATATTTT
301  CAATTGGATG TCACATTGGC GCAGCTTTAC CATCATTGGG GCTCAGTAGA
351  CAGTCATTTT CAGGAAGTAG CACAAAAGTT TCAGGGCGTC AGGTTGTTGA
401  GGCAGGACCC TATTGAGTGC CTGTTCTCAT TCATTTGTAG TTCAAACAAT
451  AATATCGCTA GGATCACTGG AATGGTTGAA AGACTGTGTC AGGCGTTTGG
501  CCCGCGACTT ATTCAATTGG ACGACGTTAC GTATCATGGC TTTCCCTCAC
551  TCCAAGCATT GGCAGGTCCT GAGGTAGAAG CACACCTGCG GAAGCTGGGC
601  TTGGGCTATA GAGCCCGCTA TGTGAGTGCT TCAGCACGCG CAATCCTGGA
651  GGAGCAAGGA GGTCTCGCGT GGCTCCAACA GCTTCGAGAG AGCTCTTATG
701  AAGAAGCACA CAAAGCTCTT TGTATTTTGC CAGGGGTAGG AACCAAGGTC
751  GCGGACTGTA TATGCCTGAT GGCTTTGGAT AAACCACAGG CGGTGCCCGT
801  TGACGTACAC ATGTGGCACA TAGCTCAGCG CGACTATTCA TGGCATCCAA
851  CAACAAGTCA AGCAAAAGGG CCAAGTCCGC AAACCAACAA GGAATTGGGA
901  AATTTCTTCC GCTCACTGTG GGGTCCCTAC GCTGGTTGGG CGCAGGCAGG
951  CCTCCTTGGC AATGCATTTG ATGGCCACCA GCTTCTGCGT CCTCTTATCT
1001 TCTGCCAGGA TCACCTCCGA GAAGGCCCCC CTATCGGGAG AGGGGATTCA
1051 CAAGGTGAAG AACTGGAACC CCAGCTTCCC TCCAGCCTCT CCTCCATTCC
1101 CTATGGGTTC TGTGACCACT GCTGGACCAA GGACGTGGAT GACCCTCCCC
1151 TAGTCACTCA TCCATCCCCT GGCTCCAGAG ATGGTCACAT GACCCAGGCC
1201 TGGCCAGTCA AAGTAGTCTC TCCCCTGGCC ACAGTAATTG GTCATGTGAT
1251 GCAAGCCAGC TTACTAGCAC TTGCGGCCGC ACTCGAGATG GACTACAAAG
1301 ACCATGACGG TGATTATAAA GATCATGACA TCGATTACAA GGATGACGAT
1351 GACAAGTAG.

The sequence codes for mitochondrial isoform of OGG1 with silent mutations to render it insensitive to all RNAi sequences mentioned above and a c-terminal FLAG-tag. The plasmid was then packaged into lentiviruses and transduced into A3 cells harbouring shRNA constructs as described above and selected with 300 μg/ml hygromycin for 10 days.

Method 3: 96-Well Cell Viability Assay

A dilution series of compound or vehicle are transferred to 96-well plates. Cells are seeded into the plate (500-10,000 cells/well) in suitable media and incubated for five days in 5% CO₂ at 37° C. Thereafter, resazurin (diluted in suitable medium or PBS) are added to a final concentration 10 μg/ml resazurin at 37° C. for 2-4 hours before measuring the fluorescence (Ex544/Em590), essentially as described (Riss, Terry L. et al., “Cell Viability Assays.” In Assay Guidance Manual, ed. G. Sitta Sittampalam, et al. Bethesda (Md.): Eli Lilly & Company and the National Center for Advancing Translational Sciences (2004) http://www.ncbi.nlm.nih.gov/books/NBK144065/).

Method 4: 384-Well Cell Viability Assay

The compounds to be tested are nano-dispensed in duplicate in 11 concentrations, directly in 384-well cell plates, with a final DMSO concentration<1%. Cells are seeded in cell plates, pre-dispensed with compounds (200-2500 cells/well in 50 μl). After three or five days culture in 5% CO2, 37° C., resazurin diluted in PBS is added, 10 μl/well, to a final concentration of 10 μg/ml and cells are incubated 2-4 hours before measuring fluorescence (Ex544/Em590), as described (ibid.). Results obtained for selected example compounds described herein on cancer- and non-transformed cell lines are provided in the table below (Table 3) and summarized in FIG. 1. Where indicated, combination indexes was measured with CompuSyn software (www.compusyn.com) by the method of Chou-Talalay (Chou, Ting-Chao., Cancer Research, 70(2), 440-46 (2010)). Table 3 shows the viability EC₅₀ values (in M) of selected example compounds on various cancer- and non-transformed cell line viability using methods 2 or 3.

TABLE 3
			EC50 (M)
Cell line	Type	Cancer/cell type	Ex. 13	Ex. 28	Ex. 50
786-0	Cancer	Renal Cell	3.0E−05	1.5E−05	3.3E−05
		Adenocarcinoma
A3	Cancer	Acute	1.1E−05	7.9E−06	9.8E−06
		lymphoblastic
		leukemia
A498	Cancer	Renal carcinoma	2.9E−05	2.1E−05	3.5E−05
A549	Cancer	Lung carcinoma	1.2E−05	1.1E−05	8.5E−06
ACHN	Cancer	Renal Cell	2.3E−06	8.5E−06	2.8E−06
		Adenocarcinoma
BJ Ras	Cancer	Transformed	4.8E−06	1.5E−05	1.4E−05
		fibroblast
BJ Tert	Normal	immortalized	3.4E−05	2.4E−05	3.1E−05
		fibroblast
CCD841	Normal	fetal epithelial	4.3E−05	4.0E−05	5.4E−05
		colon
CCRF-	Cancer	Acute	1.5E−05	1.1E−05	7.9E−06
CEM		Lymphoblastic
		Leukemia
Daudi	Cancer	Burkitt's	1.3E−05	1.0E−05	1.2E−05
		Lymphoma
DU145	Cancer	Prostate	1.3E−05	1.1E−05	3.1E−06
		carcinoma
H460	Cancer	large cell lung	1.0E−05	1.4E−05	1.7E−05
		carcinoma
HCT116	Cancer	Colorectal	1.8E−05	1.5E−05	2.9E−05
		Carcinoma
HCT116 +	Cancer	Colorectal	2.1E−05	1.7E−05	2.0E−05
Chr3		Carcinoma
Hec59	Cancer	endometrioid	1.7E−05	1.1E−05	ND
		adenocarcinoma
Hec59 +	Cancer	endometrioid	1.6E−05	1.7E−05	ND
Chr2		adenocarcinoma
HeLa	Cancer	Cervical	2.2E−05	1.6E−05	3.5E−05
		adenocarcinoma
HL-60	Cancer	Acute	2.2E−05	1.4E−05	2.4E−05
		Promyelocytic
		Leukemia
HT-29	Cancer	Colorectal	2.4E−05	2.3E−05	2.2E−05
		Adenocarcinoma
Jurkat	Cancer	Acute	1.3E−05	1.4E−05	1.5E−05
		lymphoblastic
		leukemia
K562	Cancer	Chronic	2.0E−05	2.1E−05	ND
		Myelogenous
		Leukemia
KG1a	Cancer	Acute	1.6E−05	1.8E−05	1.9E−05
		Myelogenous
		Leukemia
LCL#1	Normal	Epstein-Barr-virus-	3.3E−05	3.4E−05	4.0E−05
		transformed
		lymphoblastoid
		cell lines
LCL#2	Normal	Epstein-Barr-virus-	2.5E−05	4.1E−05	3.2E−05
		transformed
		lymphoblastoid
		cell lines
M059J	Cancer	Malignant	2.6E−05	2.1E−05	2.9E−05
		Glioblastoma
M059K	Cancer	Malignant	2.0E−05	1.9E−05	2.7E−05
		Glioblastoma
MEF Ogg1	Normal	mouse embryonic	4.8E−05	4.6E−05	3.4E−05
(−/−)		fibroblast
MOLT4	Cancer	Acute	1.5E−05	1.3E−05	1.7E−05
		Lymphoblastic
		Leukemia
MRC5	Normal	fetal lung fibroblast	7.5E−05	2.1E−05	4.7E−05
MV4-11	Cancer	acute monocytic	9.4E−06	6.5E−06	9.6E−06
		leukemia
NB-4	Cancer	acute promyelocytic	5.0E−06	1.1E−05	ND
		leukemia
PC3	Cancer	Prostate	3.5E−05	1.9E−05	2.9E−05
		adenocarcinoma
PL-21	Cancer	acute myeloid	1.5E−05	1.0E−05	1.8E−05
		leukemia
Raji	Cancer	Burkitt's	2.5E−05	2.0E−05	2.3E−05
		Lymphoma
Rec1	Cancer	Mantle Cell	1.4E−05	1.3E−05	1.5E−05
		Lymphoma
Reh	Cancer	Acute Lymphocytic	1.9E−05	1.5E−05	1.7E−05
		Leukemia
RFX393	Cancer	Renal cancer	2.0E−05	1.4E−05	1.2E−05
		cell lines
SaOS2	Cancer	Osteosarcoma	2.1E−05	1.6E−05	2.0E−05
SW1271	Cancer	Small Cell Lung	2.2E−05	2.5E−05	ND
		Carcinoma
SW480	Cancer	Colorectal	3.3E−05	2.0E−05	3.0E−05
		Adenocarcinoma
T98G	Cancer	Glioblastoma	1.4E−05	1.9E−05	1.7E−05
		Multiforme
THP1	Cancer	Acute Monocytic	2.3E−05	1.9E−05	ND
		Leukemia
U2OS	Cancer	Osteosarcoma	2.0E−05	1.6E−05	2.5E−05
UO31	Cancer	Renal carcinoma	2.9E−06	7.1E−06	3.2E−06
VH10	Normal	fibroblast	3.2E−05	2.1E−05	4.8E−05

Method 5: Suspension Cell Proliferation Assay

Cell proliferation is measured by seeding cells growing in suspension at a density of 200,000 cells/min suitable medium. The cells are incubated at 5% CO₂, 37° C. with 200 ng/ml doxycycline, 10 μM example compound or vehicle. Dead cells are stained with trypan blue, while viable cells are counted daily or at other fixed intervals. When cell populations exceed 1,000,000 cells/ml they are re-seeded into fresh medium containing fresh doxycycline, example compound or vehicle at 200,000 cells/ml. Results obtained for selected example compounds described herein on the A3 cancer cell line are shown in the FIGS. 4A and 4B.

Method 6: Colony Formation Survival Assay

Example compounds or vehicle are transferred to 6-well plates. Cell lines to be tested are seeded at a density of 200-500 cells/well in suitable media and allowed to grow for 7-11 days in at 5% CO₂, 37° C. The medium is removed and replaced with 4% w/v methylene blue in methanol. Following extensive washes in tap water and air drying, colonies with more than 50 colonies are counted, as described in Franken, Nicolaas A. P., et al., Nature Protocols, 1(5), 2315-19 (2006). Results obtained for selected example compounds described herein on the normal and cancer cell lines are shown in the FIGS. 5A and 5B.

Biological Example 3: OGG1 Inhibitor Reduce Inflammation

Method 7: OGG1 Inhibitors Preclude Pro-Inflammatory Gene Regulation

MLE-12 cells are maintained in suitable medium and treated with vehicle or 5 μM experimental compound for 48 h before stimulation with 20 ng/ml TNFα for 30 minutes. RNA is extracted and reverse-transcribed, followed by quantitative PCR evaluation of a panel of pro-inflammatory regulators (SABiosciences) essentially as described in Ba, Xueqing, et al., The Journal of Immunology, 192(5), 2384-94 (2014). Results obtained a selected example compound described herein on the pro-inflammatory gene regulation are shown in FIG. 6.

Method 8: Evaluation of In Vivo Efficiency

Six- to 8-wk-old BALB/c mice (˜20 g; Harlan Sprague Dawley, San Diego, CA) were injected 25 mg/kg intraperitoneally 3 h before and at the time of intranasal TNF-α challenge essentially as described in Ba, Xueqing, et al., The Journal of Immunology, 192(5), 2384-94 (2014). To evaluate inflammation, bronchoalveolar lavage fluids (BALF) were collected 16 h after challenge, processed, cytospin slides were stained with Wright-Giemsa, and the number of neutrophils was counted. All experiments were performed according to the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals. Results obtained a selected example compound described herein on the pro-inflammatory gene regulation are shown in FIGS. 7A and 7B.

Biological Example 4: Mouse CCL2 Assay in MLE12 Cells

Assay Principle:

Cisbio mouse CCL2 assay is intended for the quantitative measurement of CCL2 in supernatant using HTRF® technology. The assay is compatible with mouse samples, and is highly specific for CCL2. CCL2 is detected in a sandwich assay format using 2 different specific antibodies, one labeled with Cryptate (donor) and the second with d2 (acceptor). The detection principle is based on HTRF® technology. When the labelled antibodies bind to the same antigen, the excitation of the donor with a light source (laser or flash lamp) triggers a Fluorescence Resonance Energy Transfer (FRET) towards the acceptor, which in turn fluoresces at a specific wavelength (665 nm). The two antibodies bind to the CCL2 present in the sample, thereby generating FRET. Signal intensity is proportional to the number of antigen-antibody complexes formed and therefore to the CCL2 concentration.

• • Materials:
  • Cells: MLE12 (Mouse Lung Epithelial cells, SV40 transformed)
  • Medium: DMEM/F12 (Gibco #11330057), FBS 5% (Gibco #10500064), Pen/Strep 50 U/50 μg/ml (Gibco #15070063)
  • Cell plates: 384-well, black/clear, TC-treated (Corning #3764)
  • Source plate: Labcyte LDV 384 (Labcyte #LP-0200)
  • Compound dilution plate: V-bottom 384-well PP plate (Greiner #781280)
  • Compounds: 10 mM stocks in DMSO
  • HTRF plates: 384-well, white, half area, non-binding (Costar #3824)
  • Mouse CCL2 kit: Cisbio 62MCCL2PEH
  • Other reagents: Trypsin/EDTA 10× (Gibco #15400054), PBS (Gibco #14190169), Resazurin (Sigma-Aldrich #199303), 1 mg/ml in PBS, TNF-α 200 μg/ml in PBS (Peprotech #300-01A)
  • Instruments:
  • Echo liquid handler (Labcyte)
  • Multidrop Combi (Thermo Scientific)
  • Sense plate reader (Hidex)Compound Handling:

Stock solutions (10 mM in DMSO) of compounds were dispensed in V-bottom 384-well plates and the following dilutions were prepared: 10 mM and 0.05 mM. The dilutions were transferred to the source plate. Duplicate 6 points dose-response curves of compounds were nano-dispensed in cell plates (CCL2 assay) and in parallel, 11 points DR curves in duplicates were nano-dispensed for the viability assay. The plates were heat sealed and kept at RT until use.

Seeding of Cells:

MLE12 cells in flasks were washed once with PBS, detached with Trypsin/EDTA, resuspended in fresh medium and counted. Cells were diluted to 3×105 cells/ml and seeded with Multidrop Combi in cell plates pre-dispensed with compounds, 25 μl/well (7500 cells/well). The plates were placed, one by one, in a CO₂-incubator at 37° C. for 1 hour after which 25 μl/well of TNF-α (final concentration 20 ng/ml) were added. The plates were transferred back to the CO₂-incubator placed in a plastic box with wet tissue in the bottom, to avoid evaporation, for 30 hours.

mCCL2 Assay:

After 30 hours incubation, the plates were spun down 5 minutes at 400 g, and 16 μl/well of the supernatants were transferred to the assay plate. A mCCL2 standard curve was prepared according to the kit protocol and 16 μl/well of the standards were also added to the assay plate.

The anti-CCL2 antibody mix was prepared according to the kit protocol, and 4 μl/well were added to the assay plate. The plate was sealed and incubated over night at RT. After incubation the plate was read in Sense plate reader with Time-resolved FRET protocol (Ex330 nm/Em 620 and 665 nm). After data reduction, the delta ratios were imported to an excel template where the IC50 values were calculated.

Cell Viability Assay:

After 24 hours culture, resazurin reagent (stock 1 mg/ml in PBS) diluted 1:17 in PBS was added with Multidrop Combi, 10 μl/well, and plates were incubated for 6 hours. Plates were read in Sense plate reader with resorufin protocol (ex544 nm/em595 nm). The results were imported to an excel template where the EC50 values were calculated using XLfit. The results of the inflammation assay are shown in Table 4.

TABLE 4
	Cell Viability	CCL2
Example	(IC50, nM)	(EC50, nM)
2	10331	15400
13	7666	18781
20	11526	33000
22	13847	52700
23	19867	29000
26	7702	15031
27	7740	16300
28	7183	17000
37	7025	17400
39	6495	15100
41	16617	50700
49	5400	15200
50	7232	15400
72	6310	21500
75	10430	34100
75	12821	39400
77	7397	21200
82	17679	30848
83	14027	34700
84	8136	23900
85	17217	39200
86	13665	19400
87	5255	6480
89	25088	47100
91	6448	12600
92	13735	38800
93	21324	34900
94	8454	20200
107	7405	15576
107	7401	16700
117	14440	65200
118	5390	16700
119	5067	17700
121	4858	13000
122	4499	14100
123	10000	24200
124	11538	31200
126	15663	26470
127	16228	28700
129	9482	21600
130	6356	22600
131	17439	39200
135	9004	23300
136	8857	23800
139	10086	31800
140	17682	34600
142	7963	15800
146	9725	29559
147	17892	32110
148	15740	31700
149	16660	33700
150	7580	18700
151	17137	5250
152	6176	15400
153	24600	44000
154	16138	52300
160	8175	25600
164	12900	33900
166	16400	42700
168	14413	32600
171	17484	41063
183	16953	36172
184	7855	16771
187	7900	13017
191	29793	33500
192	15725	32900
194	15581	33500
197	19489	30200
199	7510	16500
201	10392	18200
202	7968	11600
204	7930	12900
206	26747	33718
209	21453	34904
212	16877	34167
221	7845	15200
225	1712	3130
226	17068	34100
227	16451	27476
228	16390	20800
228	10476	11200
229	9186	12200
229	6667	6932
230	2578	5840
237	4536	31745
238	9175	27100
240	16062	21455
243	5740	14700
244	13733	37339
245	12545	>33000
249	15729	34722
250	25986	39900
257	19902	34300
258	11339	42700
262	19672	>100000
263	27159	>33000
267	17930	34091
268	13382	>100000
269	17329	31204
270	16751	32897
271	4647	9445
272	27062	35690
273	19238	32561
274	18087	39018
276	16893	54041
277	14992	28647
280	16643	24677
281	1826	8825
282	27521	28593
283	19830	30753
285	15915	>33000
286	20295	>33000
289	24489	32073
295	10393	11100
296	13450	10500
297	28878	30800
298	29165	36569
299	10232	31665
300	1577	2110
301	16213	43041
302	14378	27200
304	8267	10600
305	4880	8110
306	7152	8075
307	28839	32044
308	215	2043
309	15568	27817
310	6129	13558
311	13768	14541
312	10982	28477
313	19546	35107

Abbreviations

The following abbreviations may be used herein:

• • APEX1 apurinic/apyrimidinic endodeoxyribonuclease 1
  • aq aqueous
  • BINAP 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl
  • Boc tert-butoxycarbonyl
  • brine saturated aqueous solution of NaCl
  • CI combination index
  • DBU 1,8-diazabicyclo[5.4.0]undec-7-ene
  • DCM dichloromethane
  • DIEA N,N-diisopropylethylamine
  • DMAP 4-dimethylaminopyridine
  • DMF dimethylformamide
  • DMSO dimethylsulfoxide
  • DTT dithiothreitol
  • EDC-HCl N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride
  • EtOAc ethyl acetate
  • EtOH ethanol
  • Ex example
  • FAM fluorescein
  • HATU O-(7-azabenzotriazolyl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate
  • HOBt 1-hydroxybenzotriazole
  • Int intermediate
  • LAH lithium aluminium hydride
  • MeCN acetonitrile
  • MeOH methanol
  • NBS N-bromosuccinimide
  • NMR nuclear magnetic resonance
  • OGG1 8-oxoguanine-DNA glycosylase 1
  • Pd₂(dba)₃ tris(dibenzylideneacetone)dipalladium(0)
  • PBS phosphate buffered saline
  • rac racemic
  • rt room temperature
  • tBuOK potassium tert-butoxide
  • tBuONa sodium tert-butoxide
  • TBS tris-buffered saline
  • TFA trifluoroacetic acid
  • THE tetrahydrofuran
  • TNFα Tumor necrosis factor alpha
  • Xantphos 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene
  • 8-oxoA 8-oxo-2′deoxyadenosine

Claims

1. A compound of formula I

2. A compound as claimed in claim 1, wherein X1 and X2 each represent O; or X1 represents O and X2 represents S.

3. A compound as claimed in claim 1, wherein Z3 represents CH or N.

4. A compound as claimed in claim 1, wherein n represents 0.

5. A compound as claimed in claim 1, wherein the compound of formula I is a compound of formula Ig

6. A compound as claimed in claim 1, wherein R2 represents: (i) phenyl optionally substituted by one to three groups independently selected from A4, (ii) 5- or 6-membered monocyclic heteroaryl optionally substituted by one to three (e.g. one to two) groups selected from oxy and A5, or(iii) phenyl substituted with two adjacent groups which, together with the ring to which they are attached, form a bicyclic heteroaryl optionally substituted by one to three (e.g. one) groups selected from oxy and A6.

7. A compound as claimed in claim 1, wherein R3 independently represents: (i) halo, —NO2, —CN, —R2a, —OR2b, —S(O)qR2c, —S(O)rN(R2d)(R2e), —N(R2f)SOsR2g, —N(R2h)(R2i), —C(O)OR2j, or —C(O)NR2kR2l;(ii) phenyl optionally substituted by one or two groups independently selected from A7; or(iii) heteroaryl (e.g. pyridinyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazolopyrimidinyl, or pyrrolopyrazolyl) optionally substituted by one group selected from A8.

8. A compound as claimed in claim 1, selected from N-(4-iodophenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,4-(4-Hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,N-(4-chlorophenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,4-(4-Fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,Methyl 2-(1-{1-[(4-iodophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)acetate4-(4-Ethoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,N-(4-iodophenyl)-4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-(4-Amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,4-(4-Dimethylamino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,N-(4-iodophenyl)-4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(4-iodophenyl)-4-[2-oxo-4-(1H-1,2,4-triazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(4-iodophenyl)-4-[4-(methylsulfanyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(4-iodophenyl)-4-[2-oxo-4-(1H-pyrrol-2-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(4-iodophenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide,4-[4-(3-Aminophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,4-[4-(2-Hydroxyethyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-iodophenyl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[2-oxo-4-(pyridin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-{4-[4-(Aminomethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,4-(1-{1-[(3,4-Dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoic acid,N-(3,4-dichlorophenyl)-4-(4-{4-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[2-oxo-4-(pyrimidin-5-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-{4-[3,5-Bis(trifluoromethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-{2-oxo-4-[4-(2,2,2-trifluoroacetyl)phenyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide,4-[4-(4-Bromo-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-iodophenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-ethylphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethoxyphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide,N-(2H-1,3-benzodioxol-5-yl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-bromo-3-methylphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-bromo-3-chlorophenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodo-3-methylphenyl)piperidine-1-carboxamide,4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)-3-trans-hydroxypiperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-{2-oxo-4-[2-(trifluoromethyl)pyridin-4-yl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide,4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[4-(2-ethoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[4-(6-methoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-{4-[3-(Carbamoylmethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,3-(1-{1-[(3,4-Dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoic acid,Methyl 3-(1-{1-[(3,4-dichlorophenyl)carbamoyl]piperidin-4-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-4-yl)benzoate,N-(3,4-dichlorophenyl)-4-(4-{3-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-{4-[3-(morpholine-4-carbonyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-(4-{3-[(2-methoxyethyl)carbamoyl]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[2-oxo-4-(4-sulfamoylphenyl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-[4-(3-fluorophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-{4-[3-(Aminomethyl)phenyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,4-[4-(2-Aminophenyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,N-(3,4-dichlorophenyl)-4-(4-{2-[(dimethylamino)methyl]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,4-(4-Bromo-2-sulfanylidene-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methyl-3-(trifluoromethyl)phenyl]piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methoxyphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-fluorophenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methylphenyl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-chloro-4-(trifluoromethoxy)phenyl]piperidine-1-carboxamide,4-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodo-3-methylphenyl)piperidine-1-carboxamide,4-{4-[6-(Hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,N-(4-Chloro-3-methoxyphenyl)-4-{4-[6-(hydroxymethyl)pyridin-3-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}piperidine-1-carboxamide,4-{4-[4-(Ethylcarbamoyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodophenyl)piperidine-1-carboxamide,4-{4-[4-(Diethylcarbamoyl)-1H-pyrazol-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(4-iodophenyl)piperidine-1-carboxamide,4-(4-(4-((2-(Dimethylamino)ethyl)carbamoyl)-1H-pyrazol-1-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide, 2,2,2-trifluoroacetate,4-(4-{4-[(2,3-Dihydroxypropyl)carbamoyl]-1H-pyrazol-1-yl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-iodophenyl)piperidine-1-carboxamide,N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,N-(3-chloro-4-methoxyphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide,4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide,N-(3-chloro-4-methoxyphenyl)-4-(2-oxo-4-{1H-pyrazolo[3,4-b]pyridin-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,N-(4-chloro-3-methoxyphenyl)-4-[2-oxo-4-(pyridin-3-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-[4-(6-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide,4-[4-(5-Aminopyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(4-chloro-3-methoxyphenyl)piperidine-1-carboxamide,N-(4-chloro-3-methoxyphenyl)-4-[4-(6-methoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(3-chloro-4-methoxyphenyl)-4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-(3-chloro-4-methoxyphenyl)-4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5,6-dichloropyridin-3-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloro-6-methylpyridin-2-yl)piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3,4-dichlorophenyl)-2-methylpiperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3,4-dichlorophenyl)-3-methylpiperidine-1-carboxamide,4-(4-Chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,4-(4-Methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)piperidine-1-carboxamide,N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(1H-pyrazol-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dichlorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-chloro-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-fluorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-cyanophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-phenylcyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-difluorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methoxy-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,4-dichlorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-cyanophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-chloro-4-(trifluoromethoxy)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chlorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-fluoro-3-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-methyl-3-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-4-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-chloro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chlorophenyl)cyclohexane-1-carboxamide,Methyl 2-methoxy-5-[(cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexaneamido]benzoate,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-fluoro-4-methylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-difluoro-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-5-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-chloro-3-cyanophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-methoxy-5-(trifluoromethyl)phenyl]cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-cyano-3-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,5-difluoro-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-cyano-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-fluorophenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-5-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxyphenyl)cyclohexane-1-carboxamide, (Cis)-N-(2H-1,3-benzodioxol-5-yl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-dimethylphenyl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-methyl-1,2-oxazol-3-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-pyrazol-4-yl)cyclohexane-1-carboxamide,(Cis)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-indazol-5-yl)cyclohexane-1-carboxamide,4-(4-Amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)piperidine-1-carboxamide,N-(3-Chloro-4-methoxyphenyl)-4-[2-oxo-4-(propylamino)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,N-(3-Chloro-4-methoxyphenyl)-4-[4-(methylsulfanyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]piperidine-1-carboxamide,4-(4-Bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-methoxyphenyl)-3-hydroxypiperidine-1-carboxamide,N-(3-Chloro-4-methoxyphenyl)-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)piperidine-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxypyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-chloropyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5,6-dichloropyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indazol-7-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-chloro-5-methylpyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloropyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-methylpyridin-2-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methylpyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-hydroxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4-dimethoxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3,4,5-trimethoxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-hydroxy-3-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-aminophenyl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-hydroxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2,3-dihydro-1,4-benzodioxin-6-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(dimethylamino)phenyl]cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methyl-1H-indazol-5-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[4-(dimethylamino)phenyl]cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-chloro-4-hydroxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(5-chloro-6-methoxypyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-methyl-1,3-benzoxazol-6-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(quinolin-6-yl)cyclohexane-1-carboxamide,Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-fluoro-4-methoxyphenyl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide,Cis-N-(1H-indol-6-yl)-4-(4-methoxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(4-methoxy-3-methylphenyl)cyclohexane-1-carboxamide,Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-fluoro-4-methoxyphenyl)cyclohexane-1-carboxamide,Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(6-methoxy-5-methylpyridin-3-yl)cyclohexane-1-carboxamide,Cis-4-(4-fluoro-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-hydroxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(2-hydroxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(2-amino-4,5-dimethylphenyl)-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,4-[cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexaneamido]benzamide,Cis-4-(4-{3-[2-(dimethylamino)ethoxy]phenyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-(4-hydroxy-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-[2-(Dimethylamino)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-(4-{[2-(dimethylamino)ethyl](methyl)amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-(4-{[(4-methoxyphenyl)methyl]sulfanyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-[3-(hydroxymethyl)phenyl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-4-sulfanyl-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,2-({2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}sulfonyl)acetic acid,Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperazin-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(morpholin-4-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,2-({2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}oxy)acetic acid,Cis-4-{4-[benzyl(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(methylamino)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(1H-indol-6-yl)-4-[4-(2-methoxyethoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,N-(2-Aminoethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N-(2,3-Dihydroxypropyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-(4-amino-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(2-methoxyacetamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,N-(2-Methanesulfonamidoethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,2-Oxo-N-[2-(piperazin-1-yl)ethyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-{4-[(2-acetamidoethyl)carbamoyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,2-Oxo-N-[(pyrrolidin-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-[4-(2-aminoacetamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-(4-bromo-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1-methyl-1H-1,3-benzodiazol-2-yl)cyclohexane-1-carboxamide,Methyl 2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxylate,N-Methyl-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N,N-Dimethyl-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperazine-1-carbonyl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(morpholine-4-carbonyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,N-(2-Hydroxyethyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-{4-[(2-carbamoylethyl)carbamoyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-(3-Aminopropyl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N-Methyl-N-[2-(methylamino)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-{4-[(3R)-3-(dimethylamino)pyrrolidine-1-carbonyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(4-methylpiperazine-1-carbonyl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-4-{4-[4-(dimethylamino)piperidine-1-carbonyl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-[(1H-Imidazol-2-yl)methyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(2S)-2-[(pyrrolidin-1-yl)methyl]pyrrolidine-1-carbonyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide,N-[2-(Morpholin-4-yl)ethyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,2-Oxo-N-[(oxolan-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[3-(trifluoromethyl)piperazine-1-carbonyl]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide,Cis-4-(4-{4-[2-(dimethylamino)ethyl]piperazine-1-carbonyl}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,2-Oxo-N-[(pyrimidin-2-yl)methyl]-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N-Methyl-N-(1-methylpyrrolidin-3-yl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,1-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carbonyl}pyrrolidine-2-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(pyrimidin-2-yl)amino]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide,Cis-4-(4-{[2-(dimethylamino)ethyl]amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,tert-Butyl N-(1-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidin-3-yl)carbamate,Cis-4-[4-(3-aminopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-{4-[2-(dimethylamino)acetamido]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-[4-(3-aminopropanamido)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-{4-[2-(morpholin-4-yl)acetamido]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide, (2S,4R)-4-Hydroxy-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidine-2-carboxamide,(2S)—N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}azetidine-2-carboxamide,Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}morpholine-2-carboxamide,Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indol-6-yl)cyclohexane-1-carboxamide,2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N-[(Morpholin-3-yl)methyl]-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,N-(Azetidin-3-yl)-2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,2-Oxo-N-(pyrrolidin-3-yl)-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazole-4-carboxamide,Cis-4-{4-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-Methoxy-4-methylphenyl)-4-{4-[methyl(1-methylpyrrolidin-3-yl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-(4-{methyl[2-(methylamino)ethyl]amino}-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-{4-[(2-aminoethyl)(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-pyrazole-3-carboxamide,5-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,2-oxazole-3-carboxamide,N-{2-Oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,3-oxazole-5-carboxamide,Cis-4-{4-[(3-aminopropyl)(methyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-[4-(4-aminopiperidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-4-{4-[2-(dimethylamino)ethoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,tert-Butyl N-{3-[methyl({2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl})amino]propyl}carbamate,Cis-4-{4-[3-(dimethylamino)propoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(piperidin-4-yloxy)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,tert-Butyl N-methyl-N-[2-({2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}oxy)ethyl]carbamate,Cis-N-(3-methoxy-4-methylphenyl)-4-{4-[2-(methylamino)ethoxy]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(pyrrolidin-1-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[2-oxo-4-(1,2,3,6-tetrahydropyridin-4-yl)-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide,Cis-4-[4-(3-acetamidopyrrolidin-1-yl)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-(2-oxo-4-{1H,4H,5H,6H-pyrrolo[3,4-c]pyrazol-5-yl}-2,3-dihydro-1H-1,3-benzodiazol-1-yl)cyclohexane-1-carboxamide,Cis-4-(4-acetamido-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl)-N-(1H-indazol-5-yl)cyclohexane-1-carboxamide,Methyl N-(1-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}pyrrolidin-3-yl)carbamate,Cis-4-{4-[3-(2-hydroxy-2-methylpropanamido)pyrrolidin-1-yl]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-imidazole-2-carboxamide,1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-imidazole-4-carboxamide,2-Amino-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1,3-oxazole-4-carboxamide,1-Methyl-N-{2-oxo-1-[cis-4-[(3-methoxy-4-methylphenyl)carbamoyl]cyclohexyl]-2,3-dihydro-1H-1,3-benzodiazol-4-yl}-1H-pyrazole-5-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-{2-oxo-4-[(2,2,2-trifluoroethyl)amino]-2,3-dihydro-1H-1,3-benzodiazol-1-yl}cyclohexane-1-carboxamideCis-4-{4-[(2,2-difluoroethyl)amino]-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl}-N-(3-methoxy-4-methylphenyl)cyclohexane-1-carboxamide,Cis-N-(3-methoxy-4-methylphenyl)-4-[4-(3-methylbutoxy)-2-oxo-2,3-dihydro-1H-1,3-benzodiazol-1-yl]cyclohexane-1-carboxamide, andCis-4-(4-(2-(cyclohexyloxy)ethoxy)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)-N-(3-methoxy-4-methylphenyl)cyclohexanecarboxamide, ora pharmaceutically acceptable salt thereof.

9. A method of treating a cell proliferation disorder comprising administering to a patient in need thereof a therapeutically effective amount of a B compound as defined in claim 1, including a pharmaceutically acceptable salt thereof, but without proviso (b).

10. A pharmaceutical composition comprising a compound as defined in claim 1, including a pharmaceutically acceptable salt thereof, and optionally one or more pharmaceutically acceptable excipient.

11. A combination product comprising: (I) a compound as defined in claim 1, including a pharmaceutically acceptable salt thereof; and(II) one or more other therapeutic agent that is useful in the treatment of a cell proliferation disorder,wherein each of components (I) and (II) is formulated in admixture, optionally with one or more a pharmaceutically acceptable excipient.

12. A kit-of-parts comprising: (a) a pharmaceutical formulation as defined in claim 10; and(b) one or more other therapeutic agent that is useful in the treatment of a cell proliferation disorder, optionally in admixture with one or more pharmaceutically acceptable excipient,which components (a) and (b) are each provided in a form that is suitable for administration in conjunction with the other.

13. A process for the preparation of a compound as defined in claim 1, comprising the step of: (i) for compounds of formula I wherein X1 represents O, reacting a compound of formula II

14. A compound as claimed in claim 1, wherein: R2a independently represents (i) C1-6 alkyl, C2-6 alkenyl or C2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B1; andeach R2b to R2l independently represents H or (i) C1-6 alkyl, C2-6 alkenyl or C2-6 alkynyl, wherein each such alkyl, alkenyl or alkynyl group is optionally substituted by one or more groups independently selected from oxy and B1.

15. A compound as claimed in claim 1, wherein: R2 represents phenyl optionally substituted by one or more groups independently selected from A4; andR3 independently represents halo, —NO2, —CN, —R2a, —OR2b, —S(O)qR2c, —S(O)rN(R2d)(R2e), —N(R2f)SOsR2g, —N(R2h)(R2i), —C(O)OR2j, or —C(O)NR2kR2l.

16. A compound as claimed in claim 1, wherein R3 represents halo, —OR2b, —N(R2h)(R2i), or —C(O)NR2kR2l.

17. A compound as claimed in claim 1, wherein R3 represents halo.