NAMPT MODULATORS

Abstract

Provided are compounds of Formula (II): or a pharmaceutically acceptable salt thereof, wherein R1, n, and Y1 are as defined herein. Also provided is a pharmaceutically acceptable composition comprising a compound of Formula (II), or a pharmaceutically acceptable salt thereof. Also provided are methods of using a compound of Formula (II), or a pharmaceutically acceptable salt thereof.

Description

FIELD

Provided herein are alkyl urea compounds, pharmaceutical compositions comprising such compounds, and methods of treating various diseases and conditions mediated by nicotinamide phosphoribosyltransferase (NAMPT) with such compounds.

BACKGROUND

The present disclosure relates to the use of modulators of nicotinamide phosphoribosyltransferase (NAMPT) and derivatives thereof, as well as enhancers or inducers of NAMPT expression, NAMPT activity or NAMPT-mediated signaling for preventing or treating a variety of pathological conditions.

Nicotinamide adenine dinucleotide (NAD+) is an essential coenzyme (enzyme cofactor) involved in fundamental biological processes of both catabolic and anabolic metabolism. As a coenzyme, NAD is associated with many oxidative enzymes (typically dehydrogenases) involved in energy metabolism, serving as a universal electron carrier. NAD exists in cells in the oxidized state (NAD+ and NADP+), and the reduced state (NADH and NADPH), acting as a chemical means to capture and transfer free energy from oxidative processes in catabolism, or to provide small packets of energy to build macromolecules in anabolism. NADH produced from the oxidation of carbohydrates, lipids, and amino acids provides reducing equivalents to the electron transport chain of mitochondria, ultimately driving the synthesis of ATP in oxidative phosphorylation.

More than 200 enzymes use either NAD+ or NADP+ as a coenzyme, and the enzymatic functions are not limited to energy metabolism. It is now appreciated that NAD+ plays a role in regulating diverse functions, including mitochondrial function, respiratory capacity, and biogenesis, mitochondrial-nuclear signaling. Further, it controls cell signaling, gene expression, DNA repair, hematopoiesis, immune function, the unfolded protein response, and autophagy. Furthermore, NAD is anti-inflammatory and is the precursor for NADPH, which is the primary source of reducing power for combating oxidative stress. A large body of literature indicates that boosting NAD levels is an effective strategy to either prevent or ameliorate a wide variety of disease states (Stremland et al., Biochem Soc Trans. 2019, 47(1):119-130; Ralto et al., Nat Rev Nephrol. 2019; Fang et al., Trends Mol Med. 2017, 23(10):899-916; Yoshino et al., Cell Metab. 2011, 14(4):528-36; Yang and Sauve, Biochim Biophys Acta. 2016, 1864:1787-1800; Verdin, Science. 2015, 350(6265):1208-13).

Levels of NAD+ and NADP+-associated enzymes play important roles in normal physiology and are altered under various disease and stress conditions including aging. Cellular NAD+ levels decrease during aging, metabolic disease, inflammatory diseases, during ischemia/reperfusion injury, and in other conditions in humans (Massudi et al., PLoS ONE. 2012, 7(7): e42357) and animals (Yang et al., Cell. 2007, 130(6):1095-107; Braidy et al. PLoS One. 2011, 26; 6(4):e19194; Peek et al. Science. 2013, 342(6158):1243417; Ghosh et al., J Neurosci. 2012, 32(17):5821-32), suggesting that modulation of cellular NAD+ level affects the speed and severity of the decline and deterioration of bodily functions. Therefore, an increase in cellular NAD+ concentration could be beneficial in the context of aging and age-related diseases.

The cellular NAD+ pool is controlled by a balance between the activity of NAD+-synthesizing and consuming enzymes. In mammals, NAD+ is synthesized from a variety of dietary sources, including one or more of its major precursors that include: tryptophan (Trp), nicotinic acid (NA), nicotinamide riboside (NR), nicotinamide mononucleotide (NMN), and nicotinamide (NAM). Based upon the bioavailability of its precursors, there are three pathways for the synthesis of NAD+ in cells: (i) from Trp by the de novo biosynthesis pathway or kynurenine pathway (ii) from NA in the Preiss-Handler pathway and (iii) from NAM, NR, and NMN in the salvage pathway (Verdin et al., Science. 2015, 350(6265):1208-13). Of these, the predominant NAD+ biosynthetic pathway involves the step of synthesis of nicotinamide mononucleotide (NMN) using nicotinamide and 5′-phosphoribosyl-pyrophosphate by the rate-limiting enzyme nicotinamide phosphoribosyl-transferase (NAMPT) that is critical to determination of longevity and responses to a variety of stresses (Fulco et al, Dev Cell. 2008, 14(5):661-73; Imai, Curr Pharm Des. 2009, 15(1):20-8; Revollo et al., J Biol Chem. 2004, 279(49):50754-63; Revollo et al., Cell Metab. 2007, November; 6(5):363-75; van der Veer et al., J Biol Chem. 2007, 282(15):10841-5; Yang et al., Cell. 2007, 130(6):1095-107). Thus, increasing the rate of NAMPT catalysis by a small molecule activator would be an effective strategy to boost NAD levels and thereby address a broad spectrum of disease states. These include cardiac diseases, chemotherapy induced tissue damage, renal diseases, metabolic diseases, muscular diseases, neurological diseases and injuries, diseases caused by impaired stem cell function, DNA damage and primary mitochondrial disorders, and ocular diseases.

SUMMARY

In one aspect, provided herein is a compound of Formula (II):

• • or a pharmaceutically acceptable salt thereof,
  • wherein:
  • n is 0 to 6;
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is —C(O)—N(R^q)—(R^s), wherein R^q is H or C₁-C₆ alkyl, and R^s is C₃-C₈ cycloalkyl, optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(optionally substituted C₆-C₁₄ aryl), and R¹ is selected from the group consisting of

• • or
  • Y¹ is —C(O)—R^b, wherein R^b is optionally substituted 3- to 18-membered heterocycloalkyl, and

R¹ is

• • or
  • Y¹ is —N(R^t)—C(O)R^u, wherein R^t is H or C₁-C₆ alkyl, and R^u is optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl), and R¹ is

• • or
  • Y¹ is

• •  and R¹ is

• •  wherein
    • R^2a and R^2b are each independently halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, or —N(R^2e)C(O)(C₁-C₆ alkyl); and
    • R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl;
    • G¹ is CH or N;
    • p1 and p2 are each independently 0, 1, or 2;
    • q1 and q2 are each independently 1 or 2;
    • r is 1, 2, or 3;
  • wherein, when Y is

• •  then n is 4, 5, or 6;
  • when Y¹ is

• •  and r is 1, then n is 2, 3, 4, 5, or 6; and
  • when Y¹ is —C(O)—N(R^q)—(R^s), —C(O)—R^b, —N(R^t)—C(O)R^u, or

• •  then n is 4 or 5;
  • R³ is selected from the group consisting of:
    • i. unsubstituted C₁-C₆ alkyl;
    • ii. C₆-C₁₄ aryl;
    • iii. optionally substituted 5- to 18-membered heteroaryl;
    • iv. —NR^3aR^3b, wherein
      • R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
      • v. —OR^3c, wherein
        • R³, is C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
      • vi. —C(O)R^3d, wherein
        • R^3d is selected from the group consisting of —NR^3fR^3g; C₃-C₈ cycloalkyl; C₃-C₈ cycloalkyl substituted with optionally substituted C₆-C₁₄ aryl; C₃-C₈ cycloalkenyl; optionally substituted C₆-C₁₄ aryl; optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl); optionally substituted 3- to 18-membered heterocycloalkyl; and optionally substituted 5- to 18-membered heteroaryl,
        • wherein
        •  R^3f and R^3g are each independently selected from the group consisting of:
        •  (a) hydrogen,
        •  (b) optionally substituted C₁-C₆ alkyl,
        •  (c) C₆-C₁₄ aryl,
        •  (d) optionally substituted 3- to 18-membered heterocycloalkyl,
        •  (e) optionally substituted 5- to 18-membered heteroaryl,
        •  (f) optionally substituted C₃-C₁₀ cycloalkyl; and
        •  (g) optionally substituted C₃-C₁₀ cycloalkenyl;
    • vii. C₁-C₆ alkyl substituted with one or more —OH, —C(O)NR^3hR³ⁱ, optionally substituted C₆-C₁₄ aryl, optionally substituted 3- to 18-membered heterocycloalkyl, optionally substituted 5- to 18-membered heteroaryl, —N(R^3p)—C(O)R^3q, —S(O)₂—R^3r, or —C(O)—R^3s,
      • wherein
        • R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl),
        • R^3p is H or C₁-C₆ alkyl,
        • R^3q is C₃-C₈ cycloalkyl, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl,
        • R^3r is C₆-C₁₄ aryl or 5- to 18-membered heteroaryl, and
        • R^3s is optionally substituted 3- to 18-membered heterocycloalkyl;
    • viii. —C(O)OR³¹, wherein
      • R^3j is hydrogen or C₁-C₆ alkyl;
    • ix. —NHC(O)R^3k, wherein
      • R^3k is optionally substituted C₆-C₁₄ aryl, optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), or optionally substituted 5- to 18-membered heteroaryl;
    • x. —NHC(O)OR³¹, wherein
      • R^3l is hydrogen or C₁-C₆ alkyl;
    • xi. —NHSO₂R^3m, wherein
      • R^3m is optionally substituted 5- to 18-membered heteroaryl, optionally substituted C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), each of which is optionally substituted; and
    • xii. —SO₂R³ⁿ; wherein
      • R³ⁿ is C₁-C₆ alkyl, optionally substituted C₃-C₁₀ cycloalkyl, optionally substituted C₆-C₁₄ aryl, or optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
  • R⁴ is phenyl or —C(O)NH—CH₂-phenyl;
  • R^5a and R^5b are independently selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl); and
  • R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), —C(O)-(optionally substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), and 5- to 18-membered heteroaryl,
    • provided that, when R⁶ is —C(O)-(substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆alkylene)-(optionally substituted 5- to 18-membered heteroaryl), or 5- to 18-membered heteroaryl, then (1) n is 4 or 5, and (2) R¹ is selected from the group consisting of

• • wherein
    • (1) when Y¹ is

• • •  and n is 0 or 1, then R¹ is selected from the group consisting of

• • •  and
    • (2) when Y¹ is

• • •  and n is 0 or 1, then R¹ is selected from the group consisting of

In one aspect, provided herein is a compound of Formula (I):

or a pharmaceutically acceptable salt thereof,

• • wherein:
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • • wherein
      • R^2a and R^2b are each independently halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, or —N(R^2e)C(O)(C₁-C₆ alkyl); and
    • R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl;
    • G¹ is CH or N;
    • p1 and p2 are each independently 0, 1, or 2;
    • q1 and q2 are each independently 1 or 2;
    • r is 1, 2, or 3;
  • n is 0 to 6;
    • wherein when Y¹ is

• • •  n is 4, 5, or 6; and
    • when Y¹ is

• • •  and r is 1, n is 2, 3, 4, 5, or 6;
  • R³ is selected from the group consisting of:
    • i. C₁-C₆ alkyl;
    • ii. C₆-C₁₄ aryl;
    • iii. optionally substituted 5- to 18-membered heteroaryl;
    • iv. —NR^3aR^3b, wherein
      • R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
    • v. —OR^3c, wherein
      • R³, is C₆-C₁₄ aryl;
    • vi. —C(O)R^3d, wherein
      • R^3d is selected from the group consisting of —NR³R³; C₃-C₈ cycloalkyl; C₃-C₈ cycloalkyl substituted with optionally substituted C₆-C₁₄ aryl; C₃-C₈ cycloalkenyl; optionally substituted C₆-C₁₄ aryl; optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl); optionally substituted 3- to 18-membered heterocycloalkyl; and optionally substituted 5- to 18-membered heteroaryl,
      • wherein
        • R^3f and R^3g are each independently selected from the group consisting of:
        • (a) hydrogen,
        • (b) optionally substituted C₁-C₆ alkyl,
        • (c) C₆-C₁₄ aryl,
        • (d) optionally substituted 3- to 18-membered heterocycloalkyl,
        • (e) optionally substituted 5- to 18-membered heteroaryl,
        • (f) optionally substituted C₃-C₁₀ cycloalkyl; and
        • (g) optionally substituted C₃-C₁₀ cycloalkenyl;
    • vii. C₁-C₆ alkyl substituted with C(O)NR^3hR³ⁱ, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl,
      • wherein R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
    • viii. —C(O)OR³¹, wherein
      • R^3j is hydrogen or C₁-C₆ alkyl;
    • ix. —NHC(O)R^3k, wherein
      • R^3k is optionally substituted C₆-C₁₄ aryl, optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), or optionally substituted 5- to 18-membered heteroaryl;
    • x. —NHC(O)OR³¹, wherein
      • R^3l is hydrogen or C₁-C₆ alkyl;
    • xi. —NHSO₂R^3m, wherein
      • R^3m is optionally substituted 5- to 18-membered heteroaryl, optionally substituted C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), each of which is optionally substituted; and
    • xii. —SO₂R³ⁿ; wherein
      • R³ⁿ is optionally substituted C₃-C₁₀ cycloalkyl, optionally substituted C₆-C₁₄ aryl, or optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
  • R⁴ is phenyl or —C(O)NH—CH₂-phenyl;
  • R^5a and R^5b are independently selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl); and
  • R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), and —C(O)-phenyl; and
  • wherein
    • (1) when Y¹ is

• • •  and n is 0 or 1, R¹ is selected from the group consisting of

• • •  and
    • (2) when Y¹ is

• • •  and n is 0, R¹ is selected from the group consisting of

In another aspect, provided herein is a compound of Formula (I-A):

or a salt thereof, wherein R¹, R³, G¹, p1, p2, q1, q2, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-B):

or a salt thereof, wherein R¹, R⁴, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-C):

or a salt thereof, wherein R¹, R^5s, R^5b, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-D):

or a salt thereof, wherein R¹, R⁶, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-E) or (I-F):

or a salt thereof, wherein R¹, n, and r are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-G):

or a salt thereof, wherein R¹, R^q, R^s, and n are as defined for Formula (II), or any variation or embodiment thereof.

In another aspect, provided herein is a compound of Formula (I-H):

or a salt thereof, wherein R¹, R^b, and n are as defined for Formula (II), or any variation or embodiment thereof.

In one aspect, provided herein is a compound of Formula (I-J):

or a salt thereof, wherein R¹, R^t, R^u, and n are as defined herein for Formula (II), or any variation or embodiment thereof.

In one aspect, provided herein is a compound of Formula (I-K):

or a salt thereof, wherein R¹ and n are as defined herein for Formula (II), or any variation or embodiment thereof.

In a further aspect, provided herein are pharmaceutical compositions comprising at least one compound of Formula (II), (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), such as a compound of Table 1, or a pharmaceutically acceptable salt of any of the foregoing, optionally further comprising a pharmaceutically acceptable excipient.

In another aspect, provided herein is a method of treating a disease or condition mediated by NAMPT activity in a subject in need thereof, comprising administering to the subject an effective amount of at least one compound Formula (II), (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), such as a compound of Table 1, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition comprising at least one compound of Formula (II), (I), (I-A), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K). In some embodiments, the disease or condition is selected from the group consisting of cancer, a hyperproliferative disease or condition, an inflammatory disease or condition, a metabolic disorder, a cardiac disease or condition, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a neurological disease or injury, a neurodegenerative disorder or disease, diseases caused by impaired stem cell function, diseases caused by DNA damage, primary mitochondrial disorders, or a muscle disease or muscle wasting disorder. In some embodiments, the disease or condition is selected from the group consisting of obesity, atherosclerosis, insulin resistance, type 2 diabetes, cardiovascular disease, Alzheimer's disease, Huntington's disease, Parkinson's disease, amyotrophic lateral sclerosis, depression, Down syndrome, neonatal nerve injury, aging, axonal degeneration, carpal tunnel syndrome, Guillain-Barre syndrome, nerve damage, polio (poliomyelitis), and spinal cord injury.

Additional embodiments, features, and advantages of the present disclosure will be apparent from the following detailed description and through practice of the present disclosure.

For the sake of brevity, the disclosures of publications cited in this specification, including patents, are herein incorporated by reference.

DETAILED DESCRIPTION

Definitions

As used in the present specification, the following words and phrases are generally intended to have the meanings as set forth below, except to the extent that the context in which they are used indicates otherwise.

Throughout this application, unless the context indicates otherwise, references to a compound of Formula (II) or Formula (I) includes all subgroups of Formula (II) or Formula (I) defined herein, including all substructures, subgenera, preferences, embodiments, examples and particular compounds defined and/or described herein. References to a compound of Formula (II) or Formula (I) and subgroups thereof, include ionic forms, polymorphs, pseudopolymorphs, amorphous forms, solvates, co-crystals, chelates, isomers, tautomers, oxides (e.g., N-oxides, S-oxides), esters, prodrugs, isotopes and/or protected forms thereof. In some embodiments, references to a compound of Formula (II) or Formula (I) and subgroups thereof, include polymorphs, solvates, co-crystals, isomers, tautomers and/or oxides thereof. In some embodiments, references to a compound of Formula (II) or Formula (I) and subgroups thereof, include polymorphs, solvates, and/or co-crystals thereof. In some embodiments, references to a compound of Formula (II) or Formula (I) and subgroups thereof, include isomers, tautomers and/or oxides thereof. In some embodiments, references to a compound of Formula (II) or Formula (I) and subgroups thereof, include solvates thereof. Similarly, the term “salts” includes solvates of salts of compounds.

“Alkyl” encompasses straight and branched carbon chains having the indicated number of carbon atoms, for example, from 1 to 20 carbon atoms, or 1 to 8 carbon atoms, or 1 to 6 carbon atoms. For example, C_1-6 alkyl encompasses both straight and branched chain alkyl of from 1 to 6 carbon atoms. When an alkyl residue having a specific number of carbons is named, all branched and straight chain versions having that number of carbons are intended to be encompassed; thus, for example, “propyl” includes n-propyl and isopropyl; and “butyl” includes n-butyl, sec-butyl, isobutyl and t-butyl. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, 2-pentyl, 3-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, and 3-methylpentyl.

As used herein, the term “haloalkyl” refers to an alkyl moiety, as described above, wherein one or more of the hydrogen atoms of the alkyl moiety has been replaced by one or more independently selected halogen atoms. By way of illustration, the term “haloalkyl” includes, but it not limited to, a methyl moiety in which one or more of the hydrogen atoms of the methyl moiety has been replaced by one or more independently selected halogen atoms, e.g., —CH₂F, —CHF₂, —CH₂Cl, —CCl₃, —CHClF, —CCl₂Br, etc.

As used herein, the term “alkoxy” refers to a —O-alkyl moiety.

As used herein, the term “haloalkoxy” refers to an alkoxy moiety, as described above, wherein one or more of the hydrogen atoms of the alkoxy moiety has been replaced by one or more independently selected halogen atoms. By way of illustration, the term “haloalkoxy” includes, but it not limited to, a methoxy moiety in which one or more of the hydrogen atoms of the methoxy moiety has been replaced by one or more independently selected halogen atoms, e.g., —O—CH₂F, —O—CHF₂, —O—CH₂Cl, —O—CCl₃, —O—CHClF, —O—CCl₂Br, etc.

As used herein, the term “alkylene” refers to divalent alkyl group as defined herein above having 1 to 20 carbon atoms. Unless otherwise provided, alkylene refers to moieties having 1 to 20 carbon atoms, 1 to 16 carbon atoms, 1 to 10 carbon atoms, 1 to 7 carbon atoms, or 1 to 4 carbon atoms. Alkylene groups include, but are not limited to, methylene, ethylene, n-propylene, iso-propylene, n-butylene, sec-butylene, iso-butylene, tert-butylene, n-pentylene, isopentylene, neopentylene, n-hexylene, 3-methylhexylene, 2,2-dimethylpentylene, 2,3-dimethylpentylene, n-heptylene, n-octylene, n-nonylene, and n-decylene.

When a range of values is given (e.g., C_1-6 alkyl), each value within the range as well as all intervening ranges are included. For example, “C_1-6 alkyl” includes C₁, C₂, C₃, C₄, C₅, C₆, C_1-6, C_2-6, C_3-6, C_4-6, C_5-6, C_1-5, C_2-5, C_3-5, C_4-5, C_1-4, C_2-4, C_3-4, C_1-3, C_2-3, and C_1-2 alkyl.

“Alkenyl” refers to an unsaturated branched or straight-chain alkyl group having the indicated number of carbon atoms (e.g., 2 to 8, or 2 to 6 carbon atoms) and at least one carbon-carbon double bond. The group may be in either the cis or trans configuration (Z or E configuration) about the double bond(s). Alkenyl groups include, but are not limited to, ethenyl, propenyl (e.g., prop-1-en-1-yl, prop-1-en-2-yl, prop-2-en-1-yl (allyl), prop-2-en-2-yl), and butenyl (e.g., but-1-en-1-yl, but-1-en-2-yl, 2-methyl-prop-1-en-1-yl, but-2-en-1-yl, but-2-en-1-yl, but-2-en-2-yl, buta-1,3-dien-1-yl, buta-1,3-dien-2-yl).

“Alkynyl” refers to an unsaturated branched or straight-chain alkyl group having the indicated number of carbon atoms (e.g., 2 to 8 or 2 to 6 carbon atoms) and at least one carbon-carbon triple bond. Alkynyl groups include, but are not limited to, ethynyl, propynyl (e.g., prop-1-yn-1-yl, prop-2-yn-1-yl) and butynyl (e.g., but-1-yn-1-yl, but-1-yn-3-yl, but-3-yn-1-yl).

“Cycloalkyl” indicates a non-aromatic, fully saturated carbocyclic ring having the indicated number of carbon atoms, for example, 3 to 10, or 3 to 8, or 3 to 6 ring carbon atoms. Cycloalkyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl, as well as bridged, caged, and spirocyclic ring groups (e.g., norbornane, bicyclo[2.2.2]octane, spiro[3.3]heptane). In addition, one ring of a polycyclic cycloalkyl group may be aromatic, provided the polycyclic cycloalkyl group is bound to the parent structure via a non-aromatic carbon. For example, a 1,2,3,4-tetrahydronaphthalen-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is a cycloalkyl group, while 1,2,3,4-tetrahydronaphthalen-5-yl (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a cycloalkyl group. Examples of polycyclic cycloalkyl groups consisting of a cycloalkyl group fused to an aromatic ring are described below.

“Cycloalkenyl” indicates a non-aromatic carbocyclic ring, containing the indicated number of carbon atoms (e.g., 3 to 10, or 3 to 8, or 3 to 6 ring carbon atoms) and at least one carbon-carbon double bond. Cycloalkenyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkenyl groups include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclopentadienyl, and cyclohexenyl, as well as bridged and caged ring groups (e.g., bicyclo[2.2.2]octene). In addition, one ring of a polycyclic cycloalkenyl group may be aromatic, provided the polycyclic alkenyl group is bound to the parent structure via a non-aromatic carbon atom. For example, inden-1-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is considered a cycloalkenyl group, while inden-4-yl (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a cycloalkenyl group. Examples of polycyclic cycloalkenyl groups consisting of a cycloalkenyl group fused to an aromatic ring are described below.

“Aryl” indicates an aromatic carbocyclic ring having the indicated number of carbon atoms, for example, 6 to 12 or 6 to 10 carbon atoms. Aryl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). In some instances, both rings of a polycyclic aryl group are aromatic (e.g., naphthyl). In other instances, polycyclic aryl groups may include a non-aromatic ring fused to an aromatic ring, provided the polycyclic aryl group is bound to the parent structure via an atom in the aromatic ring. Thus, a 1,2,3,4-tetrahydronaphthalen-5-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered an aryl group, while 1,2,3,4-tetrahydronaphthalen-1-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is not considered an aryl group. Similarly, a 1,2,3,4-tetrahydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered an aryl group, while 1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is not considered an aryl group. However, the term “aryl” does not encompass or overlap with “heteroaryl”, as defined herein, regardless of the point of attachment (e.g., both quinolin-5-yl and quinolin-2-yl are heteroaryl groups). In some instances, aryl is phenyl or naphthyl. In certain instances, aryl is phenyl. Additional examples of aryl groups comprising an aromatic carbon ring fused to a non-aromatic ring are described below.

“Heteroaryl” indicates an aromatic ring containing the indicated number of atoms (e.g., 5 to 12, or 5 to 10 membered heteroaryl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon. Heteroaryl groups do not contain adjacent S and O atoms. In some embodiments, the total number of S and O atoms in the heteroaryl group is not more than 2. In some embodiments, the total number of S and O atoms in the heteroaryl group is not more than 1. Unless otherwise indicated, heteroaryl groups may be bound to the parent structure by a carbon or nitrogen atom, as valency permits. For example, “pyridyl” includes 2-pyridyl, 3-pyridyl and 4-pyridyl groups, and “pyrrolyl” includes 1-pyrrolyl, 2-pyrrolyl and 3-pyrrolyl groups.

In some instances, a heteroaryl group is monocyclic. Examples include pyrrole, pyrazole, imidazole, triazole (e.g., 1,2,3-triazole, 1,2,4-triazole, 1,2,4-triazole), tetrazole, furan, isoxazole, oxazole, oxadiazole (e.g., 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole), thiophene, isothiazole, thiazole, thiadiazole (e.g., 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole), pyridine, pyridazine, pyrimidine, pyrazine, triazine (e.g., 1,2,4-triazine, 1,3,5-triazine) and tetrazine.

In some instances, both rings of a polycyclic heteroaryl group are aromatic. Examples include indole, isoindole, indazole, benzoimidazole, benzotriazole, benzofuran, benzoxazole, benzoisoxazole, benzoxadiazole, benzothiophene, benzothiazole, benzoisothiazole, benzothiadiazole, 1H-pyrrolo[2,3-b]pyridine, 1H-pyrazolo[3,4-b]pyridine, 3H-imidazo[4,5-b]pyridine, 3H-[1,2,3]triazolo[4,5-b]pyridine, 1H-pyrrolo[3,2-b]pyridine, 1H-pyrazolo[4,3-b]pyridine, 1H-imidazo[4,5-b]pyridine, 1H-[1,2,3]triazolo[4,5-b]pyridine, 1H-pyrrolo[2,3-c]pyridine, 1H-pyrazolo[3,4-c]pyridine, 3H-imidazo[4,5-c]pyridine, 3H-[1,2,3]triazolo[4,5-c]pyridine, 1H-pyrrolo[3,2-c]pyridine, 1H-pyrazolo[4,3-c]pyridine, 1H-imidazo[4,5-c]pyridine, 1H-[1,2,3]triazolo[4,5-c]pyridine, furo[2,3-b]pyridine, oxazolo[5,4-b]pyridine, isoxazolo[5,4-b]pyridine, [1,2,3]oxadiazolo[5,4-b]pyridine, furo[3,2-b]pyridine, oxazolo[4,5-b]pyridine, isoxazolo[4,5-b]pyridine, [1,2,3]oxadiazolo[4,5-b]pyridine, furo[2,3-c]pyridine, oxazolo[5,4-c]pyridine, isoxazolo[5,4-c]pyridine, [1,2,3]oxadiazolo[5,4-c]pyridine, furo[3,2-c]pyridine, oxazolo[4,5-c]pyridine, isoxazolo[4,5-c]pyridine, [1,2,3]oxadiazolo[4,5-c]pyridine, thieno[2,3-b]pyridine, thiazolo[5,4-b]pyridine, isothiazolo[5,4-b]pyridine, [1,2,3]thiadiazolo[5,4-b]pyridine, thieno[3,2-b]pyridine, thiazolo[4,5-b]pyridine, isothiazolo[4,5-b]pyridine, [1,2,3]thiadiazolo[4,5-b]pyridine, thieno[2,3-c]pyridine, thiazolo[5,4-c]pyridine, isothiazolo[5,4-c]pyridine, [1,2,3]thiadiazolo[5,4-c]pyridine, thieno[3,2-c]pyridine, thiazolo[4,5-c]pyridine, isothiazolo[4,5-c]pyridine, [1,2,3]thiadiazolo[4,5-c]pyridine, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, phthalazine, naphthyridine (e.g., 1,8-naphthyridine, 1,7-naphthyridine, 1,6-naphthyridine, 1,5-naphthyridine, 2,7-naphthyridine, 2,6-naphthyridine), imidazo[1,2-a]pyridine, 1H-pyrazolo[3,4-d]thiazole, 1H-pyrazolo[4,3-d]thiazole and imidazo[2,1-b]thiazole.

In other instances, polycyclic heteroaryl groups may include a non-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl) fused to a heteroaryl ring, provided the polycyclic heteroaryl group is bound to the parent structure via an atom in the aromatic ring. For example, a 4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered a heteroaryl group, while 4,5,6,7-tetrahydrobenzo[d]thiazol-5-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is not considered a heteroaryl group. Examples of polycyclic heteroaryl groups consisting of a heteroaryl ring fused to a non-aromatic ring are described below.

“Heterocycloalkyl” indicates a non-aromatic, fully saturated ring having the indicated number of atoms (e.g., 3 to 10, or 3 to 7, membered heterocycloalkyl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon. Heterocycloalkyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of heterocycloalkyl groups include oxiranyl, aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl. Examples include thiomorpholine S-oxide and thiomorpholine S,S-dioxide. Examples of spirocyclic heterocycloalkyl groups include azaspiro[3.3]heptane, diazaspiro[3.3]heptane, diazaspiro[3.4]octane, and diazaspiro[3.5]nonane. In addition, one ring of a polycyclic heterocycloalkyl group may be aromatic (e.g., aryl or heteroaryl), provided the polycyclic heterocycloalkyl group is bound to the parent structure via a non-aromatic carbon or nitrogen atom. For example, a 1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is considered a heterocycloalkyl group, while 1,2,3,4-tetrahydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a heterocycloalkyl group. Examples of polycyclic heterocycloalkyl groups consisting of a heterocycloalkyl group fused to an aromatic ring are described below.

“Heterocycloalkenyl” indicates a non-aromatic ring having the indicated number of atoms (e.g., 3 to 10, or 3 to 7, membered heterocycloalkyl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon, and at least one double bond derived by the removal of one molecule of hydrogen from adjacent carbon atoms, adjacent nitrogen atoms, or adjacent carbon and nitrogen atoms of the corresponding heterocycloalkyl. Heterocycloalkenyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of heterocycloalkenyl groups include dihydrofuranyl (e.g., 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dihydrothiophenyl (e.g., 2,3-dihydrothiophenyl, 2,5-dihydrothiophenyl), dihydropyrrolyl (e.g., 2,3-dihydro-1H-pyrrolyl, 2,5-dihydro-1H-pyrrolyl), dihydroimidazolyl (e.g., 2,3-dihydro-1H-imidazolyl, 4,5-dihydro-1H-imidazolyl), pyranyl, dihydropyranyl (e.g., 3,4-dihydro-2H-pyranyl, 3,6-dihydro-2H-pyranyl), tetrahydropyridinyl (e.g., 1,2,3,4-tetrahydropyridinyl, 1,2,3,6-tetrahydropyridinyl) and dihydropyridine (e.g., 1,2-dihydropyridine, 1,4-dihydropyridine). In addition, one ring of a polycyclic heterocycloalkenyl group may be aromatic (e.g., aryl or heteroaryl), provided the polycyclic heterocycloalkenyl group is bound to the parent structure via a non-aromatic carbon or nitrogen atom. For example, a 1,2-dihydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is considered a heterocycloalkenyl group, while 1,2-dihydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a heterocycloalkenyl group. Examples of polycyclic heterocycloalkenyl groups consisting of a heterocycloalkenyl group fused to an aromatic ring are described below.

Examples of polycyclic rings consisting of an aromatic ring (e.g., aryl or heteroaryl) fused to a non-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl) include indenyl, 2,3-dihydro-1H-indenyl, 1,2,3,4-tetrahydronaphthalenyl, benzo[1,3]dioxolyl, tetrahydroquinolinyl, 2,3-dihydrobenzo[1,4]dioxinyl, indolinyl, isoindolinyl, 2,3-dihydro-1H-indazolyl, 2,3-dihydro-1H-benzo[d]imidazolyl, 2,3-dihydrobenzofuranyl, 1,3-dihydroisobenzofuranyl, 1,3-dihydrobenzo[c]isoxazolyl, 2,3-dihydrobenzo[d]isoxazolyl, 2,3-dihydrobenzo[d]oxazolyl, 2,3-dihydrobenzo[b]thiophenyl, 1,3-dihydrobenzo[c]thiophenyl, 1,3-dihydrobenzo[c]isothiazolyl, 2,3-dihydrobenzo[d]isothiazolyl, 2,3-dihydrobenzo[d]thiazolyl, 5,6-dihydro-4H-cyclopenta[d]thiazolyl, 4,5,6,7-tetrahydrobenzo[d]thiazolyl, 5,6-dihydro-4H-pyrrolo[3,4-d]thiazolyl, 4,5,6,7-tetrahydrothiazolo[5,4-c]pyridinyl, indolin-2-one, indolin-3-one, isoindolin-1-one, 1,2-dihydroindazol-3-one, 1H-benzo[d]imidazol-2(3H)-one, benzofuran-2(3H)-one, benzofuran-3(2H)-one, isobenzofuran-1(3H)-one, benzo[c]isoxazol-3(1H)-one, benzo[d]isoxazol-3(2H)-one, benzo[d]oxazol-2(3H)-one, benzo[b]thiophen-2(3H)-one, benzo[b]thiophen-3(2H)-one, benzo[c]thiophen-1(3H)-one, benzo[c]isothiazol-3(1H)-one, benzo[d]isothiazol-3(2H)-one, benzo[d]thiazol-2(3H)-one, 4,5-dihydropyrrolo[3,4-d]thiazol-6-one, 1,2-dihydropyrazolo[3,4-d]thiazol-3-one, quinolin-4(3H)-one, quinazolin-4(3H)-one, quinazoline-2,4(1H,3H)-dione, quinoxalin-2(1H)-one, quinoxaline-2,3(1H,4H)-dione, cinnolin-4(3H)-one, pyridin-2(1H)-one, pyrimidin-2(1H)-one, pyrimidin-4(3H)-one, pyridazin-3(2H)-one, 1H-pyrrolo[3,2-b]pyridin-2(3H)-one, 1H-pyrrolo[3,2-c]pyridin-2(3H)-one, 1H-pyrrolo[2,3-c]pyridin-2(3H)-one, 1H-pyrrolo[2,3-b]pyridin-2(3H)-one, 1,2-dihydropyrazolo[3,4-d]thiazol-3-one and 4,5-dihydropyrrolo[3,4-d]thiazol-6-one. As discussed herein, whether each ring is considered an aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl group is determined by the atom through which the moiety is bound to the parent structure.

“Halogen” or “halo” refers to fluorine, chlorine, bromine or iodine.

Unless otherwise indicated, compounds disclosed and/or described herein include all possible enantiomers, diastereomers, meso isomers and other stereoisomeric forms, including racemic mixtures, optically pure forms and intermediate mixtures thereof. Enantiomers, diastereomers, meso isomers and other stereoisomeric forms can be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. Unless specified otherwise, when the compounds disclosed and/or described herein contain olefinic double bonds or other centers of geometric asymmetry, it is intended that the compounds include both E and Z isomers. When the compounds described herein contain moieties capable of tautomerization, and unless specified otherwise, it is intended that the compounds include all possible tautomers.

“Protecting group” has the meaning conventionally associated with it in organic synthesis, i.e., a group that selectively blocks one or more reactive sites in a multifunctional compound such that a chemical reaction can be carried out selectively on another unprotected reactive site, and such that the group can readily be removed after the selective reaction is complete. A variety of protecting groups are disclosed, for example, in T. H. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, Third Edition, John Wiley & Sons, New York (1999). For example, a “hydroxy protected form” contains at least one hydroxy group protected with a hydroxy protecting group. Likewise, amines and other reactive groups may similarly be protected.

The term “pharmaceutically acceptable salt” refers to a salt of any of the compounds herein which are known to be non-toxic and are commonly used in the pharmaceutical literature. In some embodiments, the pharmaceutically acceptable salt of a compound retains the biological effectiveness of the compounds described herein and are not biologically or otherwise undesirable. Examples of pharmaceutically acceptable salts can be found in Berge et al., Pharmaceutical Salts, J. Pharmaceutical Sciences, January 1977, 66(1), 1-19. Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids. Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and phosphoric acid. Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, pyruvic acid, lactic acid, oxalic acid, malic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethylsulfonic acid, p-toluenesulfonic acid, stearic acid and salicylic acid. Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases. Inorganic bases from which salts can be derived include, for example, sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, and aluminum. Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines; substituted amines including naturally occurring substituted amines; cyclic amines; and basic ion exchange resins. Examples of organic bases include isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, and ethanolamine. In some embodiments, the pharmaceutically acceptable base addition salt is selected from ammonium, potassium, sodium, calcium, and magnesium salts.

If the compound described herein is obtained as an acid addition salt, the free base can be obtained by basifying a solution of the acid salt. Conversely, if the compound is a free base, an addition salt, particularly a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds (see, e.g., Berge et al., Pharmaceutical Salts, J. Pharmaceutical Sciences, January 1977, 66(1), 1-19). Those skilled in the art will recognize various synthetic methodologies that may be used to prepare pharmaceutically acceptable addition salts.

A “solvate” is formed by the interaction of a solvent and a compound. Suitable solvents include, for example, water and alcohols (e.g., ethanol). Solvates include hydrates having any ratio of compound to water, such as monohydrates, dihydrates and hemi-hydrates.

The term “substituted” means that the specified group or moiety bears one or more substituents including, but not limited to, substituents such as alkoxy, acyl, acyloxy, carbonylalkoxy, acylamino, amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, cycloalkyl, cycloalkenyl, aryl, heteroaryl, aryloxy, cyano, azido, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, cycloalkyl, cycloalkenyl, alkyl, alkenyl, alkynyl, heterocycloalkyl, heterocycloalkenyl, aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo, carbonylalkylenealkoxy and the like. The term “unsubstituted” means that the specified group bears no substituents. Where the term “substituted” is used to describe a structural system, the substitution is meant to occur at any valency-allowed position on the system. When a group or moiety bears more than one substituent, it is understood that the substituents may be the same or different from one another. In some embodiments, a substituted group or moiety bears from one to five substituents. In some embodiments, a substituted group or moiety bears one substituent. In some embodiments, a substituted group or moiety bears two substituents. In some embodiments, a substituted group or moiety bears three substituents. In some embodiments, a substituted group or moiety bears four substituents. In some embodiments, a substituted group or moiety bears five substituents.

By “optional” or “optionally” is meant that the subsequently described event or circumstance may or may not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. For example, “optionally substituted alkyl” encompasses both “alkyl” and “substituted alkyl” as defined herein. It will be understood by those skilled in the art, with respect to any group containing one or more substituents, that such groups are not intended to introduce any substitution or substitution patterns that are sterically impractical, synthetically non-feasible, and/or inherently unstable. It will also be understood that where a group or moiety is optionally substituted, the disclosure includes both embodiments in which the group or moiety is substituted and embodiments in which the group or moiety is unsubstituted.

The compounds disclosed and/or described herein can be enriched isotopic forms, e.g., enriched in the content of ²H, ³H, ¹¹C, ¹³C and/or ¹⁴C. In one embodiment, the compound contains at least one deuterium atom. Such deuterated forms can be made, for example, by the procedure described in U.S. Pat. Nos. 5,846,514 and 6,334,997. Such deuterated compounds may improve the efficacy and increase the duration of action of compounds disclosed and/or described herein. Deuterium substituted compounds can be synthesized using various methods, such as those described in: Dean, D., Recent Advances in the Synthesis and Applications of Radiolabeled Compounds for Drug Discovery and Development, Curr. Pharm. Des., 2000; 6(10); Kabalka, G. et al., The Synthesis of Radiolabeled Compounds via Organometallic Intermediates, Tetrahedron, 1989, 45(21), 6601-21; and Evans, E., Synthesis of radiolabeled compounds, J. Radioanal. Chem., 1981, 64(1-2), 9-32.

The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable excipient” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in pharmaceutical compositions is contemplated. Supplementary active ingredients can also be incorporated into the pharmaceutical compositions.

The terms “patient,” “individual,” and “subject” refer to an animal, such as a mammal, bird, or fish. In some embodiments, the patient or subject is a mammal. Mammals include, for example, mice, rats, dogs, cats, pigs, sheep, horses, cows and humans. In some embodiments, the patient or subject is a human, for example a human that has been or will be the object of treatment, observation or experiment. The compounds, compositions and methods described herein can be useful in both human therapy and veterinary applications.

As used herein, the term “therapeutic” refers to the ability to modulate nicotinamide phosphoribosyltransferase (NAMPT). As used herein, “modulation” refers to a change in activity as a direct or indirect response to the presence of a chemical entity as described herein, relative to the activity of in the absence of the chemical entity. The change may be an increase in activity or a decrease in activity, and may be due to the direct interaction of the chemical entity with the a target or due to the interaction of the chemical entity with one or more other factors that in turn affect the target's activity. For example, the presence of the chemical entity may, for example, increase or decrease the target activity by directly binding to the target, by causing (directly or indirectly) another factor to increase or decrease the target activity, or by (directly or indirectly) increasing or decreasing the amount of target present in the cell or organism.

The term “therapeutically effective amount” or “effective amount” refers to that amount of a compound disclosed and/or described herein that is sufficient to affect treatment, as defined herein, when administered to a patient in need of such treatment. A therapeutically effective amount of a compound may be an amount sufficient to treat a disease responsive to modulation of nicotinamide phosphoribosyltransferase (NAMPT). The therapeutically effective amount will vary depending upon, for example, the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, the particular compound, the dosing regimen to be followed, timing of administration, the manner of administration, all of which can readily be determined by one of ordinary skill in the art. The therapeutically effective amount may be ascertained experimentally, for example by assaying blood concentration of the chemical entity, or theoretically, by calculating bioavailability.

“Treatment” (and related terms, such as “treat”, “treated”, “treating”) includes one or more of: preventing a disease or disorder (i.e., causing the clinical symptoms of the disease or disorder not to develop); inhibiting a disease or disorder; slowing or arresting the development of clinical symptoms of a disease or disorder; and/or relieving a disease or disorder (i.e., causing relief from or regression of clinical symptoms). The term encompasses situations where the disease or disorder is already being experienced by a patient, as well as situations where the disease or disorder is not currently being experienced but is expected to arise. The term covers both complete and partial reduction or prevention of the condition or disorder, and complete or partial reduction of clinical symptoms of a disease or disorder. Thus, compounds described and/or disclosed herein may prevent an existing disease or disorder from worsening, assist in the management of the disease or disorder, or reduce or eliminate the disease or disorder. When used in a prophylactic manner, the compounds disclosed and/or described herein may prevent a disease or disorder from developing or lessen the extent of a disease or disorder that may develop.

Compounds

Compounds and salts thereof (such as pharmaceutically acceptable salts) are detailed herein, including in the Brief Summary and in the appended claims. Also provided are the use of all of the compounds described herein, including any and all stereoisomers, including geometric isomers (cis/trans), E/Z isomers, enantiomers, diastereomers, and mixtures thereof in any ratio including racemic mixtures, salts and solvates of the compounds described herein, as well as methods of making such compounds. Any compound described herein may also be referred to as a drug.

In one aspect, provided herein is a compound of Formula (II):

• • or a pharmaceutically acceptable salt thereof,
  • wherein:
  • n is 0 to 6;
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is —C(O)—N(R^q)—(R^s), wherein R^q is H or C₁-C₆ alkyl, and R^s is C₃-C₈ cycloalkyl, optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(optionally substituted C₆-C₁₄ aryl), and R¹ is selected from the group consisting of

• • or
  • Y¹ is —C(O)—R^b, wherein R^b is optionally substituted 3- to 18-membered heterocycloalkyl, and
  • R¹ is

• • or
  • Y¹ is —N(R^t)—C(O)R^u, wherein R^t is H or C₁-C₆ alkyl, and R^u is optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl), and R¹ is

• • or
  • Y¹ is

• •  and R¹ is

• •  wherein
    • R^2a and R^2b are each independently halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, or —N(R^2e)C(O)(C₁-C₆ alkyl); and
    • R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl;
    • G¹ is CH or N;
    • p1 and p2 are each independently 0, 1, or 2;
    • q1 and q2 are each independently 1 or 2;
    • r is 1, 2, or 3;
    • wherein, when Y is

• • •  then n is 4, 5, or 6;
    • when Y¹ is

• • •  and r is 1, then n is 2, 3, 4, 5, or 6; and
    • when Y¹ is —C(O)—N(R^q)—(R^s), —C(O)—R^b, —N(R^t)—C(O)R^u, or

• • •  then n is 4 or 5;
  • R³ is selected from the group consisting of:
    • i. unsubstituted C₁-C₆ alkyl;
    • ii. C₆-C₁₄ aryl;
    • iii. optionally substituted 5- to 18-membered heteroaryl;
    • iv. —NR^3aR^3b, wherein
      • R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
    • v. —OR^3c, wherein
      • R³, is C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
    • vi. —C(O)R^3d, wherein
      • R^3d is selected from the group consisting of —NR^3fR^3g; C₃-C₈ cycloalkyl; C₃-C₈ cycloalkyl substituted with optionally substituted C₆-C₁₄ aryl; C₃-C₈ cycloalkenyl; optionally substituted C₆-C₁₄ aryl; optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl); optionally substituted 3- to 18-membered heterocycloalkyl; and optionally substituted 5- to 18-membered heteroaryl,
      • wherein
        • R^3f and R^3g are each independently selected from the group consisting of:
        • (a) hydrogen,
        • (b) optionally substituted C₁-C₆ alkyl,
        • (c) C₆-C₁₄ aryl,
        • (d) optionally substituted 3- to 18-membered heterocycloalkyl,
        • (e) optionally substituted 5- to 18-membered heteroaryl,
        • (f) optionally substituted C₃-C₁₀ cycloalkyl; and
        • (g) optionally substituted C₃-C₁₀ cycloalkenyl;
    • vii. C₁-C₆ alkyl substituted with one or more —OH, —C(O)NR^3hR³ⁱ, optionally substituted C₆-C₁₄ aryl, optionally substituted 3- to 18-membered heterocycloalkyl, optionally substituted 5- to 18-membered heteroaryl, —N(R^3p)—C(O)R³, —S(O)₂—Rr, or —C(O)—R^s,
      • wherein
        • R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl),
        • R^3p is H or C₁-C₆ alkyl,
        • R^3q is C₃-C₈ cycloalkyl, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl,
        • R^3r is C₆-C₁₄ aryl or 5- to 18-membered heteroaryl, and
        • R^3s is optionally substituted 3- to 18-membered heterocycloalkyl;
    • viii. —C(O)OR^3j, wherein
      • R^3j is hydrogen or C₁-C₆ alkyl;
    • ix. —NHC(O)R^3k, wherein
      • R^3k is optionally substituted C₆-C₁₄ aryl, optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), or optionally substituted 5- to 18-membered heteroaryl;
    • x. —NHC(O)OR^3j, wherein
      • R³¹ is hydrogen or C₁-C₆ alkyl;
    • xi. —NHSO₂R^3m, wherein
      • R^3m is optionally substituted 5- to 18-membered heteroaryl, optionally substituted C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), each of which is optionally substituted; and
    • xii. —SO₂R³ⁿ; wherein
      • R³ⁿ is C₁-C₆ alkyl, optionally substituted C₃-C₁₀ cycloalkyl, optionally substituted C₆-C₁₄ aryl, or optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
  • R⁴ is phenyl or —C(O)NH—CH₂-phenyl;
  • R^5a and R^5b are independently selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl); and
  • R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), —C(O)-(optionally substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), and 5- to 18-membered heteroaryl
    • provided that, when R⁶ is —C(O)-(substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆alkylene)-(optionally substituted 5- to 18-membered heteroaryl), or 5- to 18-membered heteroaryl, then (1) n is 4 or 5, and (2) R¹ is selected from the group consisting of

• • wherein
    • (1) when Y¹ is

• • •  and n is 0 or 1, then R¹ is selected from the group consisting of

• • •  and
    • (2) when Y¹ is

• • •  and n is 0 or 1, then R¹ is selected from the group consisting of

In one aspect, provided are compounds of Formula (I):

• • or a pharmaceutically acceptable salt thereof,
  • wherein:
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • wherein
    • R^2a and R^2b are each independently halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, or —N(R^2e)C(O)(C₁-C₆ alkyl); and
    • R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl;
    • G¹ is CH or N;
    • p1 and p2 are each independently 0, 1, or 2;
    • q1 and q2 are each independently 1 or 2;
    • r is 1, 2, or 3;
  • n is 0 to 6;
    • wherein when Y¹ is

• • •  n is 4, 5, or 6; and
    • when Y¹ is

• • •  and r is 1, n is 2, 3, 4, 5, or 6;
  • R³ is selected from the group consisting of:
    • i. C₁-C₆ alkyl;
    • ii. C₆-C₁₄ aryl;
    • iii. optionally substituted 5- to 18-membered heteroaryl;
    • iv. —NR^3aR^3b, wherein
      • R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
    • v. —OR^3c, wherein
      • R³, is C₆-C₁₄ aryl;
    • vi. —C(O)R^3d, wherein
      • R^3d is selected from the group consisting of —NR^3fR^3g; C₃-C₈ cycloalkyl; C₃-C₈ cycloalkyl substituted with optionally substituted C₆-C₁₄ aryl; C₃-C₈ cycloalkenyl; optionally substituted C₆-C₁₄ aryl; optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl); optionally substituted 3- to 18-membered heterocycloalkyl; and optionally substituted 5- to 18-membered heteroaryl,
      • wherein
        • R^3f and R^3g are each independently selected from the group consisting of:
        • (a) hydrogen,
        • (b) optionally substituted C₁-C₆ alkyl,
        • (c) C₆-C₁₄ aryl,
        • (d) optionally substituted 3- to 18-membered heterocycloalkyl,
        • (e) optionally substituted 5- to 18-membered heteroaryl,
        • (f) optionally substituted C₃-C₁₀ cycloalkyl; and
        • (g) optionally substituted C₃-C₁₀ cycloalkenyl;
    • vii. C₁-C₆ alkyl substituted with C(O)NR^3hR³ⁱ, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl,
      • wherein R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
    • viii. —C(O)OR^3j, wherein
      • R^3j is hydrogen or C₁-C₆ alkyl;
    • ix. —NHC(O)R^3k, wherein
      • R^3k is optionally substituted C₆-C₁₄ aryl, optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), or optionally substituted 5- to 18-membered heteroaryl;
    • x. —NHC(O)OR³¹, wherein
      • R^3l is hydrogen or C₁-C₆ alkyl;
    • xi. —NHSO₂R^3m, wherein
      • R^3m is optionally substituted 5- to 18-membered heteroaryl, optionally substituted C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), each of which is optionally substituted; and
    • xii. —SO₂R³ⁿ; wherein
      • R³ⁿ is optionally substituted C₃-C₁₀ cycloalkyl, optionally substituted C₆-C₁₄ aryl, or optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
  • R⁴ is phenyl or —C(O)NH—CH₂-phenyl;
  • R^5a and R^5b are independently selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl); and
  • R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), and —C(O)-phenyl.

In some embodiments of Formula (II) or Formula (I): (1) when Y¹ is

and n is 0 or 1, then R¹ is selected from the group consisting of

and (2) when Y¹ is

and n is 0, then R¹ is selected from the group consisting of

In some embodiments of Formula (II) or Formula (I), Y¹ is

In some embodiments, Y¹ is

In some embodiments, Y¹ is

In other embodiments, Y¹ is

In some embodiments of Formula (II), Y¹ is

—C(O)—N(R^q)—(R^s), —C(O)—R^b, —N(R^t)—C(O)R^u, or

In some embodiments of Formula (II), Y¹ is —C(O)—N(R^q)—(R^s), —C(O)—R^b, —N(R^t)—C(O)R^u, or

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-A):

or a salt thereof, wherein R¹, R³, G¹, p1, p2, q1, q2, and n are as defined for Formula (II) or Formula (I), or any variation or embodiment thereof.

In some embodiments of Formula (II), Formula (I), or Formula (I-A), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2a is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R^2a is halo or —O(C₁-C₆ alkyl). In some embodiments, R^2a is halo. In some embodiments, R^2a is methoxy.

In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments, the compound of Formula (I-A) is a compound of Formula (I-A1) or (I-A2):

or a salt thereof, wherein R^2a, R^2b, R³, G¹, p1, p2, q1, q2, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), G¹ is CH. In some embodiments, G¹ is N.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), p1 is 0, 1, or 2. In some embodiments, p1 is 0. In some embodiments, p1 is 1. In some embodiments, p1 is 2. In some embodiments, p2 is 0, 1, or 2. In some embodiments, p2 is 0. In some embodiments, p2 is 2. In some embodiments, p2 is 2. In some embodiments, q1 is 1 or 2. In some embodiments, q1 is 1. In other embodiments, q1 is 2. In some embodiments, q2 is 1 or 2. In some embodiments, q2 is 1. In other embodiments, q2 is 2.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), p1 is 1 and q1 is 1. In some embodiments, p1 is 2 and q1 is 1. In some embodiments, p1 is 2 and q1 is 2. In some embodiments, p2 is 1 and q2 is 1. In some embodiments, p2 is 0 and q2 is 1. In some embodiments, p2 is 1 and q2 is 2.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl. For instance, in some embodiments, R³ is methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl, sec-butyl, or isobutyl. In some embodiments, R³ is methyl. In some embodiments, R³ is C₆-C₁₄ aryl. In some embodiments, R³ is phenyl or napthyl. In some embodiments, R³ is phenyl. In some embodiments, R³ is a 5- to 18-membered heteroaryl optionally substituted with C₁-C₆ alkyl. In some embodiments, R³ is a 5- to 6-membered heteroaryl optionally substituted with C₁-C₆ alkyl. In some embodiments, R³ is pyridyl or pyrimidyl optionally substituted with C₁-C₆ alkyl. In certain embodiments, R³ is pyridyl substituted with methyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —NR^3aR^3b, wherein R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl). In some embodiments, R³ is —NR^3aR^3b, wherein R^3a is hydrogen and R^3b is selected from the group consisting of C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl). In some embodiments, R³ is —NR^3aR^3b, wherein R^3a is hydrogen and R^3b is selected from the group consisting of 5- to 6-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 6-membered heteroaryl). In some embodiments, R³ is —NR^3aR^3b, wherein R^3a and R^3b are each —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl). In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is OR^3c, wherein R³, is C₆-C₁₄ aryl. In some embodiments, R³, is phenyl or napthyl. In some embodiments, R³ is —O-phenyl. In some embodiments, R³, is C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl).

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d. In some embodiments, R^3d is —NR^3fR^3g and R^3f and R^3g are each independently selected from the group consisting of: (a) hydrogen, (b) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of —OH, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl, wherein the C₆-C₁₄ aryl and 5- to 18-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, and CN, (c) C₆-C₁₄ aryl, (d) 3- to 18-membered heterocycloalkyl, (e) 5- to 18-membered heteroaryl optionally substituted with methyl or CN, (f) C₃-C₁₀ cycloalkyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl; and (g) C₃-C₁₀ cycloalkenyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl. In some embodiments, R^3d is —NR^3fR³, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g are each independently selected from the group consisting of: (b) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of —OH, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl, wherein the C₆-C₁₄ aryl and 5- to 18-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, and CN, (c) C₆-C₁₄ aryl, (d) 3- to 18-membered heterocycloalkyl, (e) 5- to 18-membered heteroaryl optionally substituted with methyl or CN, (f) C₃-C₁₀ cycloalkyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl; and (g) C₃-C₁₀ cycloalkenyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d, R^3d is —NR^3fR^3g, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl, wherein the C₆-C₁₄ aryl and 5- to 18-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, and CN. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, phenyl, and 5- to 6-membered heteroaryl, wherein the phenyl and 5- to 6-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, and CN. In some embodiments, R^3f is hydrogen and R^3g is C₁-C₆ alkyl substituted with one or more substituents selected from the group consisting of hydroxyl, phenyl, pyrazolyl, pyridyl, and pyrimidyl, wherein the phenyl, pyrazolyl, pyridyl, and pyrimidyl are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, and CN. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d, R^3d is —NR^3fR^3gR^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₆-C₁₄ aryl. In some embodiments, R^3f is H or C₁-C₆ alkyl, and R^3g is phenyl or napthyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d, R^3d is —NR^3fR^3gR^3f is hydrogen or C₁-C₆ alkyl, and R^3g is 3- to 18-membered heterocycloalkyl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is 3- to 18-membered heterocycloalkyl optionally substituted with halo, hydroxyl, and —(C₁-C₆ alkylene)-OH. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d, R^3d is —NR^3fR^3g, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is 5- to 10-membered heteroaryl optionally substituted with methyl or CN. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is pyridyl or pyrimidyl, each optionally substituted with methyl or CN. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d, R^3d is —NR^3fR^3gR^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₃-C₁₀ cycloalkyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl. In other embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R³ is C₃-C₁₀ cycloalkenyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₃-C₁₀ cycloalkyl optionally substituted with C₆-C₁₄ aryl or 5- to 18-membered heteroaryl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₃-C₈ cycloalkyl optionally substituted with C₆-C₁₀ aryl or 5- to 6-membered heteroaryl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is cyclobutyl optionally substituted with C₆-C₁₀ aryl or 5- to 6-membered heteroaryl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₃-C₈ cycloalkyl optionally substituted with phenyl or pyridyl. In some embodiments, R^3f is hydrogen or C₁-C₆ alkyl, and R^3g is C₃-C₁₀ cycloalkenyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with halo, hydroxyl, and —(C₁-C₆ alkylene)-OH.

In some embodiments, In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is C₃-C₈ cycloalkyl. In some embodiments, R³ is —C(O)R^3d and R^3d is C₃-C₈ cycloalkyl substituted with C₆-C₁₄ aryl, wherein the C₆-C₁₄ aryl is optionally substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆ alkoxy. In some embodiments, R³ is —C(O)R^3d and R^3d is C₃-C₈ cycloalkyl substituted with C₆-C₁₀ aryl. In some embodiments, R³ is

In some embodiments, R³ is —C(O)R^3d and R^3d is C₃-C₈ cycloalkenyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is C₆-C₁₄ aryl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, cyano, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkyl, —(C₁-C₆alkylene)-OH, —C(O)O(C₁-C₆ alkyl), —NR^3e1R^3e2, —S(O)₂(C₁-C₆ alkyl), 5- to 18-membered heteroaryl, and 3- to 18-membered heterocycloalkyl optionally substituted with oxo, wherein R^3e1 and R^3e2 are each independently H or C₁-C₆ alkyl. In some embodiments, R³ is —C(O)R^3d and R^3d is phenyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, cyano, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkyl, —(C₁-C₆ alkylene)-OH, —C(O)O(C₁-C₆ alkyl), —NR^3eR^3e2, —S(O)₂(C₁-C₆ alkyl), 5- to 18-membered heteroaryl, and 3- to 18-membered heterocycloalkyl optionally substituted with oxo, wherein R^3e1 and R^3e2 are each independently H or C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) optionally substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆ alkoxy. In some embodiments, R³ is —C(O)R^3d and R^3d is —(C₁-C₆ alkylene)-phenyl optionally substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆ alkoxy In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is 3- to 18-membered heterocycloalkyl optionally substituted with one or more substituents selected from the group consisting of (a) C₁-C₆ alkyl optionally substituted with one or more substituents independently selected from the group consisting of hydroxyl, halo, C₃-C₁₀ cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents; (b) C₆-C₁₄ aryl; (c) 3- to 18-membered heterocycloalkyl; (d) —C(O)O(C₁-C₆ alkyl); (e) —C(O)(C₆-C₁₄ aryl); (f) halo; (g) C₁-C₆ alkoxy optionally substituted with one or more halo substituents; and (h) oxo.

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is 3- to 18-membered heterocycloalkyl optionally substituted with one or more substituents selected from the group consisting of (a) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, C₃-C₁₀ cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents, (b) C₆-C₁₄ aryl, (c) 3- to 18-membered heterocycloalkyl, (d) —C(O)O(C₁-C₆ alkyl), (e) —C(O)(C₆-C₁₄ aryl), (f) halo, and (g) C₁-C₆ alkoxy optionally substituted with one or more halo substituents. In some embodiments, R³ is —C(O)R^3d and R^3d is 4- to 10-membered heterocycloalkyl optionally substituted with one or more substituents selected from the group consisting of (a) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, C₃-C₁₀ cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents, (b) C₆-C₁₄ aryl, (c) 3- to 18-membered heterocycloalkyl, (d) —C(O)O(C₁-C₆ alkyl), (e) —C(O)(C₆-C₁₄ aryl), (f) halo, and (g) C₁-C₆ alkoxy optionally substituted with one or more halo substituents. In some embodiments, R³ is —C(O)R^3d and R^3d is azetidinyl, pyrrolidinyl, piperazinyl, piperadinyl, indolinyl, isoindoyl, isoindolinyl, dihydroindenyl, tetrahydroquinolinyl, dihydrobenzooxazinyl, or tetrahydronaphthyridinyl, each optionally substituted with one or more substituents selected from the group consisting of (a) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, C₃-C₁₀ cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents, (b) C₆-C₁₄ aryl, (c) 3- to 18-membered heterocycloalkyl, (d) —C(O)O(C₁-C₆ alkyl), (e) —C(O)(C₆-C₁₄ aryl), (f) halo, and (g) C₁-C₆ alkoxy optionally substituted with one or more halo substituents. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —C(O)R^3d and R^3d is 5- to 18-membered heteroaryl optionally substituted with one or more substituents selected from the group consisting of C₁-C₆ alkyl, hydroxyl, oxo, and 3- to 18-membered heterocycloalkyl. In some embodiments, R³ is —C(O)R^3d and R^3d is 5- to 6-membered heteroaryl optionally substituted with one or more substituents selected from the group consisting of C₁-C₆ alkyl, hydroxyl, oxo, and 3- to 18-membered heterocycloalkyl. In some embodiments, R³ is —C(O)R^3d and R^3d pyridyl optionally substituted with one or more substituents selected from the group consisting of C₁-C₆ alkyl, hydroxyl, oxo, and 3- to 18-membered heterocycloalkyl. In some embodiments, R³ is —C(O)R^3d and R^3d pyridyl substituted with methyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl substituted with C(O)NR^3hR³ⁱ, wherein R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl). In some embodiments, R³ is

In some embodiments of Formula (II) (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl substituted with 3- to 18-membered heterocycloalkyl, wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more substituents independently selected from halo, oxo, C₁-C₆ alkyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl. In some embodiments, R³ is C₁-C₆ alkyl substituted with 3- to 18-membered heterocycloalkyl, wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more substituents selected from halo and C₆-C₁₄ aryl. In some embodiments, R³ is C₁-C₆ alkyl substituted with 5- to 10-membered heterocycloalkyl, wherein the 5- to 10-membered heterocycloalkyl is optionally substituted with C₆-C₁₄ aryl.

In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments, R³ is C₁-C₆ alkyl, wherein the C₁-C₆ alkyl of R³ is (i) substituted with 5- to 18-membered heteroaryl, wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more C₁-C₆ alkyl, C₆-C₁₄ aryl, or cyano, and (ii) optionally substituted with one or more —OH. In some embodiments, R³ is C₁-C₆ alkyl substituted with 5- to 18-membered heteroaryl. R³ is C₁-C₆ alkyl substituted with 5- to 10-membered heteroaryl. In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —O C(O)OR^3j, wherein R^3j is hydrogen or C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —NHC(O)R^3k. In some embodiments, R^3k is C₆-C₁₄ aryl optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxyl, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R^3k is phenyl optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxyl, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments, R^3k is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R^3k is —(C₁-C₆ alkylene)-phenyl, optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments, R^3k is 5- to 18-membered heteroaryl optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R^3k is 5- to 6-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents. In some embodiments, R^3k is pyridyl optionally substituted with C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —NHC(O)OR^3l, wherein R^3l is hydrogen or C₁-C₆ alkyl. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —NHSO₂R^3m, wherein R^3m is 5- to 18-membered heteroaryl, C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the 5- to 18-membered heteroaryl, the C₆-C₁₄ aryl, and the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) are each optionally substituted with one or more substituents selected from halo and C₁-C₆ alkoxy. In some embodiments, R³ is —NHSO₂R^3m, wherein R^3m is 5- to 18-membered heteroaryl, optionally substituted with one or more substituents selected from halo and C₁-C₆ alkoxy. In some embodiments, R³ is —NHSO₂R^3m, wherein R^3m is C₆-C₁₄ aryl, optionally substituted with one or more substituents selected from halo and C₁-C₆ alkoxy. In some embodiments, R³ is —NHSO₂R^3m, wherein R^3m is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), optionally substituted with one or more substituents selected from halo and C₁-C₆ alkoxy. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —SO₂R³ⁿ and R³ⁿ is C₁-C₆ alkyl, C₃-C₁₀ cycloalkyl, C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the C₃-C₁₀ cycloalkyl, the C₆-C₁₄ aryl, and the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) of R³ⁿ are each independently optionally substituted with one or more substituents independently selected from halo and —C(O)O(C₁-C₆ alkyl). In some embodiments, R³ is —SO₂R³ⁿ and R³ⁿ is C₁-C₆ alkyl. In some embodiments, R³ is —SO₂R³ⁿ and R³ⁿ is methyl. In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is —SO₂R³ⁿ and R³ⁿ is C₃-C₁₀ cycloalkyl, C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the C₃-C₁ cycloalkyl, the C₆-C₁₄ aryl, and the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) are each optionally substituted with one or more substituents selected from halo and —C(O)O(C₁-C₆ alkyl). In some embodiments, R³ is —SO₂R³ⁿ and R³ⁿ is C₃-C₁₀ cycloalkyl optionally substituted with one or more substituents selected from halo and —C(O)O(C₁-C₆ alkyl). In some embodiments, R³ is —SO₂R³ⁿ and R³ⁿ is C₆-C₁₄ aryl optionally substituted with one or more substituents selected from halo and —C(O)O(C₁-C₆ alkyl). In some embodiments, R³ is —SO₂R³ⁿ and R³ⁿ is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) optionally substituted with one or more substituents selected from halo and —C(O)O(C₁-C₆ alkyl). In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl substituted with one or more —N(R^3P)—C(O)R^3q, wherein R^3p is H or C₁-C₆ alkyl, and R^3q is C₃-C₈ cycloalkyl, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl. In some embodiments, R^3p is H or C₁-C₆ alkyl, and R^3q is (i) C₃-C₈ cycloalkyl, (ii) 3- to 18-membered heterocycloalkyl optionally substituted with one or more independently selected C₁-C₆ alkyl or oxo substituents, or (iii) 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments of the foregoing, R^3p is H or methyl. In some embodiments, R^3p is H. In some embodiments, R^3p is methyl. In some embodiments, R^3q is C₃-C₈ cycloalkyl. In some embodiments, R^3q is C₅-C₆ cycloalkyl. In some embodiments, R^3q is cyclopentyl. In some embodiments, R³ is

In some embodiments, R^3q is 3- to 18-membered heterocycloalkyl optionally substituted with one or more independently selected oxo substituents. In some embodiments, R^3q is 5- to 6-membered heterocycloalkyl optionally substituted with one or more independently selected oxo substituents. In some embodiments, R^3q is tetrahydropyranyl, tetrahydrothiopyranyl, or piperidinyl optionally substituted with one or more independently selected oxo substituents. In some embodiments, R³ is

In some embodiments, R^3q is 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R^3q is 5- to 6-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R^3q is pyridinyl or pyrazolyl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl substituted with one or more —S(O)₂—R^3r, wherein R^3r is C₆-C₁₄ aryl or 5- to 18-membered heteroaryl. In some embodiments, R^3r is C₆-C₁₄ aryl. In some embodiments, R^3r is phenyl. In some embodiments, R³ is

In some embodiments, R^3r is 5- to 18-membered heteroaryl. In some embodiments, R^3r is 5- to 6-membered heteroaryl. In some embodiments, R^3r is pyridinyl. In some embodiments, R³ is

In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl substituted with one or more —C(O)—R^3s, wherein R^3s is R^3s is optionally substituted 3- to 18-membered heterocycloalkyl. In some embodiments, R^3s is 3- to 18-membered heterocycloalkyl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents, wherein the C₁-C₆ alkyl is independently optionally substituted with one or more —OH. In some embodiments, R^3S is 5- to 6-membered heterocycloalkyl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents, wherein the C₁-C₆ alkyl is independently optionally substituted with one or more —OH. In some embodiments, R^3s is piperazinyl or pyrrolidinyl optionally substituted with one or more independently selected C₁-C₆alkyl substituents, wherein the C₁-C₆ alkyl is independently optionally substituted with one or more —OH. In some embodiments, R³ is

In some embodiments of Formula (II), (I), (I-A), (I-A1), or (I-A2), R³ is C₁-C₆ alkyl, wherein the C₁-C₆ alkyl of R³ is substituted with one or more independently selected optionally substituted C₆-C₁₄ aryl substituents. In some embodiments, R³ is C₁-C₆ alkyl, wherein the C₁-C₆ alkyl of R³ is (i) substituted with one or more independently selected C₆-C₁₄ aryl substituents, wherein the C₆-C₁₄ aryl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents, and (ii) optionally substituted with one or more —OH. In some embodiments, R³ is

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-B):

or a salt thereof, wherein R¹, R⁴, and n are as defined for Formula (II) or Formula (I), or any variation or embodiment thereof.

In some embodiments of Formula (I-B), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of Formula (I-B), R¹ is selected from the group consisting of

In some embodiments of Formula (I-B), R¹ is selected from the group consisting of

In some embodiments of Formula (I-B), n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In some embodiments of Formula (I-B), R⁴ is phenyl. In other embodiments, R⁴ is —C(O)NH—CH₂-phenyl. In some embodiments of Formula (I-B), when R⁴ is phenyl and n is 0, R¹ is selected from the group consisting of

In some embodiments of Formula (I-B), when R⁴ is phenyl and n is 0, R¹ is selected from the group consisting of

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-C):

or a salt thereof, wherein R¹, R^5a, R^5b, and n are as defined for Formula (II) or Formula (I), or any variation or embodiment thereof.

In some embodiments of Formula (I-C), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of Formula (I-C), R¹ is selected from the group consisting of

In some embodiments of Formula (I-C), R¹ is selected from the group consisting of

In some embodiments of Formula (I-C), n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In some embodiments of Formula (I-C), when one of R^5a and R^5b is H and the other of R^5a and R^5b is methyl, and n is 0, R¹ is selected from the group consisting of

In some embodiments of Formula (I-C), when one of R^5a and R^5b is H and the other of R^5a and R^5b is methyl, and n is 0, R¹ is selected from the group consisting of

In some embodiments of Formula (I-C, R^5a is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl). In some embodiments, R^5b is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl). In some embodiments, R^5a is hydrogen and R^5b is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl). In some embodiments, R^5a and R^5b are each methyl.

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-D):

or a salt thereof, wherein R¹, R⁶, and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In some embodiments of Formula (I-D), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of Formula (I-D), R¹ is selected from the group consisting of

In some embodiments of Formula (I-D), R¹ is selected from the group

In some embodiments of Formula (I-D), R¹ is selected from the group consisting of

In some embodiments of Formula (I-D), R¹ is

In some embodiments of Formula (I-D), R¹ is

In some embodiments of Formula (I-D), n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In some embodiments of Formula (I-D), R⁶ is —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), —C(O)-(optionally substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), and 5- to 18-membered heteroaryl. In some embodiments, R⁶ is (a) —C(O)OC(CH₃)₃; (b) —NHC(O)O(C₁-C₆ alkyl); (c) —C(O)-(phenyl), wherein the phenyl is optionally substituted with one or more substituents independently selected from C₁-C₆ alkyl, C₁-C₆ haloalkyl, and 5- to 18-membered heteroaryl; (d) —C(O)—(C₁-C₆alkylene)-(phenyl), wherein the phenyl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents; (e) —C(O)-(3- to 18-membered heterocycloalkyl), wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more independently selected oxo or C₁-C₆ alkyl substituents; (f) —C(O)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents; (g) —C(O)—(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents; or (h) 5- to 18-membered heteroaryl. In some embodiments, R⁶ is —C(O)-(optionally substituted phenyl). In some embodiments, R⁶ is —C(O)-(phenyl), wherein the phenyl is optionally substituted with one or more C₁-C₆ alkyl, C₁-C₆ haloalkyl, or 5- to 18-membered heteroaryl. In some embodiments, R⁶ is

In some embodiments of Formula (I-D), R⁶ is —C(O)OC(CH₃)₃. In some embodiments, R⁶ is —NHC(O)O(C₁-C₆ alkyl). In some embodiments, R⁶ is —C(O)—(C₁-C₆ alkylene)-(phenyl), wherein the phenyl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R⁶ is —C(O)-(3- to 18-membered heterocycloalkyl), wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more independently selected oxo or C₁-C₆ alkyl substituents. In some embodiments, R⁶ is —C(O)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R⁶ is —C(O)—(C₁-C₆alkylene)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R⁶ is 5- to 18-membered heteroaryl.

In some embodiments of Formula (I-D), R⁶ is —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), or —C(O)-(phenyl), and n is 0-6. In some embodiments of Formula (I-D), R⁶ is —C(O)-(substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), or 5- to 18-membered heteroaryl, and n is 4 or 5. In some embodiments, R⁶ is

and n is 4 or 5. In some embodiments, R⁶ is

and n is 4. In some embodiments, R⁶ is

and n is 5.

In some embodiments of Formula (I-D), R⁶ is —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), or —C(O)-(phenyl); n is 0-6; and R¹ is selected from the group consisting of

In some embodiments of Formula (I-D), R⁶ is —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), or —C(O)-(phenyl); n is 0-6; and R¹ is selected from the group consisting of

In some embodiments of Formula (I-D), R⁶ is —C(O)-(substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), or 5- to 18-membered heteroaryl; n is 4 or 5; and R¹ is selected from the group consisting of

In some embodiments of Formula (I-D), R⁶ is —C(O)-(substituted phenyl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted phenyl), —C(O)-(optionally substituted 3- to 18-membered heterocycloalkyl), —C(O)-(optionally substituted 5- to 18-membered heteroaryl), —C(O)—(C₁-C₆ alkylene)-(optionally substituted 5- to 18-membered heteroaryl), or 5- to 18-membered heteroaryl; n is 4 or 5; and R¹ is selected from the group consisting of

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-E):

or a salt thereof, wherein R¹ and n are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In some embodiments of Formula (I-E), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2a is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of Formula (I-E), n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In another aspect, the compound of Formula (II) or Formula (I) is a compound of Formula (I-F):

or a salt thereof, wherein R¹, n, and r are as defined for Formula (II) or Formula (I) or any variation or embodiment thereof.

In some embodiments of Formula (I-F), R¹ is

In some embodiments, R¹ is

In some embodiments, R¹ is

wherein R^2a is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

wherein R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl); and R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl. In some embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of Formula (I-F), r is 1. In some embodiments, r is 2. In other embodiments, r is 3.

In some embodiments of Formula (I-F), n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In other embodiments, n is 6. n is 4. In some embodiments, n is 5. In other embodiments, n is 6.

In some embodiments of Formula (I-F), r is 1 and n is 2, 3, 4, 5, or 6. In some embodiments, r is 2 and n is 0, 1, 2, 3, 4, 5, or 6. In other embodiments, r is 3 and n is 0, 1, 2, 3, 4, 5, or 6.

In another aspect, the compound of Formula (II) is a compound of Formula (I-G):

or a salt thereof, wherein R¹, R^q, R^s, and n are as defined for Formula (II) or any variation or embodiment thereof.

In some embodiments of Formula (I-G), R^q is H or C₁-C₆ alkyl, and R^s is C₃-C₈ cycloalkyl, optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(optionally substituted C₆-C₁₄ aryl). In some embodiments, R^q is H. In some embodiments, R^q is C₁-C₆ alkyl. In some embodiments, R^q is methyl. In some embodiments, R^s is C₃-C₈ cycloalkyl. In some embodiments, R^s is cyclopentyl or cyclohexyl. In some embodiments of Formula (II), Y¹ is

In some embodiments, R^s is optionally substituted C₆-C₁₄ aryl. In some embodiments, R^s is C₆-C₁₄ aryl optionally substituted with one or more substituents independently selected from halo, C₁-C₆ alkyl, and C₆-C₁₄ aryl. In some embodiments of Formula (II), Y¹ is

In some embodiments, R^s is optionally substituted 5- to 18-membered heteroaryl. In some embodiments, R^s is 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl. In some embodiments, R^s is pyridinyl optionally substituted with one or more C₁-C₆ alkyl. In some embodiments of Formula (II), Y¹ is

In some embodiments, R^s is —(C₁-C₆ alkylene)-(optionally substituted C₆-C₁₄ aryl). In some embodiments, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the C₆-C₁₄ aryl of the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) is optionally substituted with one or more C₁-C₆ alkyl. In some embodiments, R^s is, —(C₁-C₆ alkylene)-(phenyl), wherein the phenyl of the —(C₁-C₆ alkylene)-(phenyl) is optionally substituted with one or more C₁-C₆ alkyl. In some embodiments of Formula (11), Y¹ is

In some embodiments of Formula (11), Y¹ is

In some embodiments of Formula (I-G), R¹ is selected from the group consisting of

In some embodiments, R¹ is

In some embodiments of Formula (I-G), n is 4 or 5. In some embodiments, n is 4. In some embodiments, n is 5.

In another aspect, provided herein is a compound of Formula (I-H):

or a salt thereof, wherein R¹, R^b, and n are as defined for Formula (II), or any variation or embodiment thereof.

In some embodiments of Formula (I-H), R^b is optionally substituted 3- to 18-membered heterocycloalkyl. In some embodiments, R^b is 3- to 18-membered heterocycloalkyl optionally substituted with one or more C₁-C₆ alkyl, wherein the C₁-C₆ alkyl is optionally substituted with one or more —OH. In some embodiments, R^b is 6- to 10-membered heterocycloalkyl optionally substituted with one or more C₁-C₆ alkyl, wherein the C₁-C₆ alkyl is optionally substituted with one or more —OH. In some embodiments, R^b is 1,2,3,4-tetrahydroquinolinyl, morpholinyl, or piperazinyl, each independently optionally substituted with one or more C₁-C₆ alkyl, wherein the C₁-C₆ alkyl is optionally substituted with one or more —OH. In some embodiments of Formula (II), Y¹ is

In some embodiments of Formula (I-H), R¹ is

In some embodiments of Formula (I-H), n is 4 or 5. In some embodiments, n is 4. In some embodiments, n is 5.

In another aspect, provided herein is a compound of Formula (I-J):

or a salt thereof, wherein R¹, R^t, R^u, and n are as defined herein for Formula (II), or any variation or embodiment thereof.

In some embodiments of Formula (I-J), R^t is H or C₁-C₆ alkyl. In some embodiments, R^t is H. In some embodiments, R^t is C₁-C₆ alkyl. In some embodiments, R^t is methyl. In some embodiments, R^u is optionally substituted C₆-C₁₄ aryl, optionally substituted 5- to 18-membered heteroaryl, or —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl). In some embodiments, R^u is (a) C₆-C₁₄ aryl optionally substituted with one or more independently selected C₁-C₆ alkyl or halo substituents; (b) 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents; or (c) —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl). In some embodiments, R^u is C₆-C₁₄ aryl optionally substituted with one or more independently selected halo substituents. In some embodiments, R^u is phenyl optionally substituted with one or more independently selected C₁-C₆ alkyl or halo substituents. In some embodiments of Formula (II), Y¹ is

In some embodiments, R^u is 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆alkyl substituents. In some embodiments, R^u is 5- to 6-membered heteroaryl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments, R^u is pyridinyl optionally substituted with one or more independently selected C₁-C₆ alkyl substituents. In some embodiments of Formula (II), Y¹ is

In some embodiments, R^u is —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl). In some embodiments, R^u is —(C₁-C₆ alkylene)-(pyridinyl). In some embodiments of Formula (II), Y¹ is

In some embodiments of Formula (II), Y¹ is

In some embodiments of Formula (I-J), R¹ is

In some embodiments of Formula (I-J), n is 4 or 5. In some embodiments, n is 4. In some embodiments, n is 5.

In one aspect, provided herein is a compound of Formula (I-K):

or a salt thereof, wherein R¹ and n are as defined herein for Formula (II), or any variation or embodiment thereof.

In some embodiments of Formula (I-K), R¹ is

In some embodiments of Formula (I-K), n is 4 or 5. In some embodiments, n is 4. In some embodiments, n is 5.

In some embodiments, provided herein are compounds, and salts thereof, described in Table 1.

TABLE 1
Compound
No.	Structure	Name
1		1-(4-(1- benzoylpiperidin-4- yl)butyl)-3-(pyridin- 4-ylmethyl)urea
2		tert-butyl (6-(3-(4- carbamoylbenzyl)urei- do)spiro[3.3]heptan- 2-yl)carbamate
3		4-((3-(4,4- dimethylcyclohexyl) ureido)methyl)benza- mide
4		4-((3-(3- phenylcyclobutyl)urei- do)methyl)benzamide
5		tert-butyl 4-(3-(4- carbamoylbenzyl)urei- do)piperidine-1- carboxylate
6		tert-butyl (6-(3- (pyridin-4- ylmethyl)ureido)spiro [3.3]heptan-2- yl)carbamate
7		tert-butyl (6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptan- 2-yl)carbamate
8		tert-butyl (6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)carbamate
9		tert-butyl (6-(3-(4- (hydroxymethyl)ben- zyl)ureido)spiro[3.3] heptan-2- yl)carbamate
10		terr-butyl (6-(3- ((1H-pyrazol-4- yl)methyl)ureido)spi- ro[3.3]heptan-2- yl)carbamate
11		tert-butyl (6-(3- (oxazol-5- ylmethyl)ureido)spiro [3.3]heptan-2- yl)carbamate
12		tert-butyl (4-(3-(4- carbamoylbenzyl)urei- do)cyclohexyl)car- bamate
13		4-((3-(1- benzoylpiperidin-4- yl)ureido)methyl)ben- zamide
14		N-(6-(3-(4- carbamoylbenzyl)urei- do)spiro[3.3]heptan- 2-yl)benzamide
15		N-(6-(3-(pyridin-4- ylmethyl)ureido)spiro [3.3]heptan-2- yl)benzamide
16		1-(4-(1- benzoylpiperidin-4- yl)butyl)-3-(4- chlorobenzyl)urea
17		N-(6-(3-((1H- pyrazol-4- yl)methyl)ureido)spi- ro[3.3]heptan-2- yl)benzamide
18		N-(6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptan- 2-yl)benzamide
19		4-((3-(4-(1- benzoylpiperidin-4- yl)butyl)ureido)meth- yl)benzamide
20		1-(4-(1- benzoylpiperidin-4- yl)butyl)-3-(4- methoxybenzyl)urea
21		4-((3-((1r,3r)-3- (benzylcarbamoyl)cy- clobutyl)ureido)meth- yl)benzamide
22		1-(4-(1- benzylpiperidin-4- yl)butyl)-3-(4- (hydroxymethyl)ben- zyl)urea
23		1-(4-(1- benzoylpiperidin-4- yl)butyl)-3-(oxazol- 5-ylmethyl)urea
24		4-((3-(6- (benzylamino)spiro[3.3] heptan-2- yl)ureido)methyl)ben- zamide
25		tert-butyl 1-((3- (pyridin-4- ylmethyl)ureido)meth- yl)-6- azaspiro[2.5]octane- 6-carboxylate
26		4-((3-(6-(pyridin-2- ylamino)spiro[3.3]hep- tan-2- yl)ureido)methyl)ben- zamide
27		tert-butyl 1-((3-(4- chlorobenzyl)ureido) methyl)-6- azaspiro[2.5]octane- 6-carboxylate
28		tert-butyl 1-((3-(4- methoxybenzyl)urei- do)methyl)-6- azaspiro[2.5]octane- 6-carboxylate
29		tert-butyl 1-((3-(4- (hydroxymethyl)ben- zyl)ureido)methyl)- 6- azaspiro[2.5]octane- 6-carboxylate
30		tert-butyl 1-((3- (oxazol-5- ylmethyl)ureido)meth- yl)-6- azaspiro[2.5]octane- 6-carboxylate
31		tert-butyl 1-((3- ((1H-pyrazol-4- yl)methyl)ureido)meth- yl)-6- azaspiro[2.5]octane- 6-carboxylate
32		tert-butyl 1-((3-(4- acetamidobenzyl)urei- do)methyl)-6- azaspiro[2.5]octane- 6-carboxylate
33		tert-butyl 1-((3-(4- carbamoylbenzyl)urei- do)methyl)-6- azaspiro[2.5]octane- 6-carboxylate
34		4-((3-(6-((pyridin-2- ylmethyl)amino)spiro [3.3]heptan-2- yl)ureido)methyl)ben- zamide
35		methyl 6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxylate
36		tert-butyl (5-(3-(4- methoxybenzyl)urei- do)pentyl)carbamate
37		tert-butyl 6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.3]heptane- 2-carboxylate
38		1-(2-(2-(2- fluorophenyl)acetyl)- 2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
39		1-(2-(2-(2- chlorophenyl)acetyl)- 2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
40		1-(4- methoxybenzyl)-3- (2-(2-(2- methoxyphenyl)acetyl)- 2- azaspiro[3.3]heptan- 6-yl)urea
41		1-(4- methoxybenzyl)-3- (2-(2-(2- (trifluoromethyl)phe- nyl)acetyl)-2- azaspiro[3.3]heptan- 6-yl)urea
42		1-(4- methoxybenzyl)-3- (2-(2-(o- tolyl)acetyl)-2- azaspiro[3.3]heptan- 6-yl)urea
43		6-(3-(4- methoxybenzyl)urei- do)-N-(1- phenylcyclopropyl)spi- ro[3.3]heptane-2- carboxamide
44		1-(4- methoxybenzyl)-3- (6-(2- phenylpyrrolidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
45		(R)-6-(3-(4- methoxybenzyl)urei- do)-N-(1- phenylethyl)spiro[3.3] heptane-2- carboxamide
46		(S)-N-(2-hydroxy-1- phenylethyl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
47		(S)-6-(3-(4- methoxybenzyl)urei- do)-N-(1- phenylethyl)spiro[3.3] heptane-2- carboxamide
48		1-(4- methoxybenzyl)-3- (6-(2- phenylazetidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
49		6-(3-(4- methoxybenzyl)urei- do)-N-(pyridin-3- ylmethyl)spiro[3.3]hep- tane-2- carboxamide
50		6-(3-(4- methoxybenzyl)urei- do)-N-(pyridin-4- ylmethyl)spiro[3.3]hep- tane-2- carboxamide
51		N-benzyl-6-(3-(4- methoxybenzyl)urei- do)-N- methylspiro[3.3]heptane- 2-carboxamide
52		1-(4- methoxybenzyl)-3- (6-((2- phenylpyrrolidin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
53		(R)-N-(1-(2- fluorophenyl)ethyl)- 6-(3-(4- methoxybenzyl)urei- do)-N- methylspiro[3.3]heptane- 2-carboxamide
54		6-(3-(4- methoxybenzyl)urei- do)-N-(2-methyl-2- (o- tolyl)propyl)spiro[3.3] heptane-2- carboxamide
55		N-(2-(2- fluorophenyl)-2- methylpropyl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
56		6-(3-(4- methoxybenzyl)urei- do)-N-(pyridin-2- ylmethyl)spiro[3.3]hep- tane-2- carboxamide
57		1-(4- methoxybenzyl)-3- (6-(3- phenylpyrrolidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
58		1-(4- methoxybenzyl)-3- (6-(2-(pyridin-4- yl)pryrrolidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
59		(R)-1-(4- methoxybenzyl)-3- (6-(2-(pyridin-3- yl)pyrrolidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
60		(S)-N-(1-(2- fluorophenyl)ethyl)- 6-(3-(4- methoxybenzyl)urei- do)-N- methylspiro[3.3]heptane- 2-carboxamide
61		1-(4- methoxybenzyl)-3- (6-(3- phenylazetidine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
62		1-(6-(4- benzoylpiperazine- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
63		6-(3-(4- methoxybenzyl)urei- do)-N-((1r,3r)-3- phenylcyclobutyl)spi- ro[3.3]heptane-2- carboxamide
64		6-(3-(4- methoxybenzyl)urei- do)-N-(2-(2- methoxyphenyl)-2- methylpropyl)spiro[3.3] heptane-2- carboxamide
65		6-(3-(4- methoxybenzyl)urei- do)-N-(2-methyl-2- (pyridin-2- yl)propyl)spiro[3.3]hep- tane-2- carboxamide
66		6-(3-(4- methoxybenzyl)urei- do)-N-(2-methyl-2- (pyridin-3- yl)propyl)spiro[3.3]hep- tane-2- carboxamide
67		N-benzyl-2-(6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptan- 2-yl)-N- methylacetamide
68		N-benzyl-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
69		6-(3-(4- methoxybenzyl)urei- do)-N- phenethylspiro[3.3]hep- tane-2- carboxamide
70		6-(3-(4- methoxybenzyl)urei- do)-N-(2- phenylpropan-2- yl)spiro[3.3]heptane- 2-carboxamide
71		1-(4- methoxybenzyl)-3- (6-(1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
72		1-(4- methoxybenzyl)-3- (6-(7- (trifluoromethyl)- 1,2,3,4- tetrahydroisoquinoline- 2- carbonyl)spiro[3.3]hep- tan-2-y)urea
73		1-(6-(isoindoline-2- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
74		1-(6-(indoline-1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
75		N-(2-(1H-pyrazol-4- yl)ethyl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
76		1-(6-(4-(2-hydroxy- 2- methylpropyl)pipera- zine-1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
77		N-(4-cyano-2- fluorobenzyl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
78		6-(3-(4- methoxybenzyl)urei- do)-N-(3-(pyridin-4- yl)cyclobutyl)spiro[3.3] heptane-2- carboxamide
79		(R)-6-(3-(4- methoxybenzyl)urei- do)-N-methyl-N- (tetrahydrofuran-3- yl)spiro[3.3]heptane- 2-carboxamide
80		6-(3-(4- methoxybenzyl)urei- do)-N-(2-methyl-2- (pyridin-4- yl)propyl)spiro[3.3]hep- tane-2- carboxamide
81		tert-butyl (2r,4s)-2- (3-(4- methoxybenzyl)urei- do)-6- azaspiro[3.4]octane- 6-carboxylate
82		tert-butyl (2s4r)-2- (3-(4- methoxybenzyl)urei- do)-6- azaspiro[3.4]octane- 6-carboxylate
83		tert-butyl 6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.4]octane- 2-carboxylate
84		1-(4- methoxybenzyl)-3- (6-(6-methyl- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
85		1-(6-(3,4-dihydro- 2H- benzo[b][1,4]oxazine- 4- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
86		6-(3-(4- methoxybenzyl)urei- do)-N- phenylspiro[3.3]heptane- 2-carboxamide
87		6-(3-(4- methoxybenzyl)urei- do)-N-methyl-N- phenylspiro[3.3]heptane- 2-carboxamide
88		N-((2- (difluoromethoxy)py- ridin-4-yl)methyl)-6- (3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
89		N- ([1,2,4]triazolo[4,3- a]pyridin-6-yl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
90		1-(4- methoxybenzyl)-3- (6-(1,2,3,4- tetrahydro-1,6- naphthyridine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
91		(R)-N-(2,3-dihydro- 1H-inden-1-yl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
92		S)-N-(2,3-dihydro- 1H-inden-1-yl)-6-(3- (4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
93		N-(3- (hydroxymethyl)- 2,3-dihydro-1H- inden-1-yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
94		N-(1-hydroxy-2,3- dihydro-1H-inden-2- yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
95		N-(2,3-dihydro-1H- inden-2-yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
96		(R)-6-(3-(4- methoxybenzyl)urei- do)-N-(1,2,3,4- tetrahydronaphthalen- 2- yl)spiro[3.3]heptane- 2-carboxamide
97		(S)-N-(7-fluoro- 1,2,3,4- tetrahydronaphthalen- 1-yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
98		(S)-N-(6-fluoro- 1,2,3,4- tetrahydronaphthalen- 1-yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
99		(R)-N-(7-fluoro- 1,2,3,4- tetrahydronaphthalen- 1-yl)-6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2-carboxamide
100		(R)-6-(3-(4- methoxybenzyl)urei- do)-N-(1,2,3,4- tetrahydronaphthalen- 1- yl)spiro[3.3]heptane- 2-carboxamide
101		1-(6-(6-fluoro- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
102		1-(6-(7,8-difluoro- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
103		1-(6-(6- (difluoromethoxy)- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
104		1-(4- methoxybenzyl)-3- (6-(6- (trifluoromethyl)- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
105		1-(6-(5-fluoro- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
106		1-(6-(7-fluoro- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
107		1-(4- methoxybenzyl)-3- (6-(6- (trifluoromethoxy)- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
108		1-(4- methoxybenzyl)-3- (6-(7-methyl- 1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
109		1-(4-fluorobenzyl)- 3-(6-(4-(2-hydroxy- 2- methylpropyl)pipera- zine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
110		1-(4-chlorobenzyl)- 3-(6-(4-(2-hydroxy- 2- methylpropyl)pipera- zine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
111		1-(4- methoxybenzyl)-3- (6-(4-(oxetan-3- yl)piperazine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
112		1-(6-(4- (cyclopropylmethyl)- piperazine-1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
113		1-(6-(2- (hydroxymethyl)-4- methylpiperazine-1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
114		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- y)benzamide
115		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- phenylacetamide
116		1-(2-((2- chlorophenyl)sulfonyl)- 2- azaspiro[3.3.]heptan- 6-yl)-3-(4- methoxybenzyl)urea
117		1-(2-((2- chlorobenzyl)sulfonyl)- 2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
118		1-(2-((2- chlorophenethyl)sulfo- nyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
119		1-(4-chlorobenzyl)- 3-(6- (dibenzylamino)spiro [3.3]heptan-2- yl)urea
120		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-1-(2- chlorophenyl)methane- sulfonamide
121		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)benzenesulfonamide
122		1-(6-(4- isopropylpiperazine- 1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
123		1-(4- methoxybenzyl)-3- (6-(4-((1-methyl- 1H-pyrazol-4- yl)methyl)piperazine- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
124		1-(4- methoxybenzyl)-3- (6-(4-(pyridin-4- ylmethyl)piperazine- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
125		1-(4- methoxybenzyl)-3- (6-(4-(pyridin-2- ylmethyl)piperazine- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
126		1-(6-(3- (hydroxymethyl)-4- methylpiperazine-1- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
127		1-(6-((5,7-difluoro- 3,4-dihydroquinolin- 1(2H)- yl)methyl)spiro[3.3] heptan-2-yl)-3-(4- methoxybenzyl)urea
128		1-(6-(indolin-1- ylmethyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
129		1-(6-(isoindolin-2- ylmethyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
130		1-(4- (bicyclo[2.2.1]heptan- 2-ylsulfonyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
131		methyl 4-((6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.3]heptan- 2- yl)sulfonyl)cyclohex- ane-1-carboxylate
132		N-(6-cyanopyridin- 2-yl)-6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.3]heptane- 2-carboxamide
133		6-(3-(4- methoxybenzyl)urei- do)-N-(2- methylpyrimidin-5- yl)-2- azaspiro[3.3]heptane- 2-carboxamide
134		1-(6-((1H-indazol-1- yl)methyl)spiro[3.3] heptan-2-yl)-3-(4- methoxybenzyl)urea
135		1-(2-(3-(2- chlorophenyl)pro- panoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
136		tert-butyl 3-(6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.3]heptane- 2- carbonyl)piperidine- 1-carboxylate
137		1-(4- methoxybenzyl)-3- (2-(1,2,3,4- tetrahydronaphthalene- 1-carbonyl)-2- azaspiro[3.3]heptan- 6-yl)urea
138		1-(4- methoxybenzyl)-3- (2-(6- methylnicotinoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
139		1-(2-isonicotinoyl-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
140		1-(4- methoxybenzyl)-3- (2-(2- methylisonicotinyl)- 2- azaspiro[3.3]heptan- 6-yl)urea
141		1-(2-benzoyl-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
142		1-(4- methoxybenzyl)-3- (2-(2-methyl-2- phenylpropanoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
143		1-(4- methoxybenzyl)-3- (2-(1- phenylcyclopropane- 1-carbonyl)-2- azaspiro[3.3]heptan- 6-yl)urea
144		1-(4- methoxybenzyl)-3- (2-(1-methyl-6-oxo- 1,6-dihydropyridine- 3-carbonyl)-2- azaspiro[3.3]heptan- 6-yl)urea
145		1-(4- methoxybenzyl)-3- (2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
146		1-(4- methoxybenzyl)-3- (2-(3- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
147		1-(4- methoxybenzyl)-3- (2-(4- (trifluoromethyl)ben- zoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
148		1-(4- methoxybenzyl)-3- (2-(2- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
149		1-(4- methoxybenzyl)-3- (5- phenoxypentyl)urea
150		1-(4- methoxybenzyl)-3- (6- phenoxyhexyl)urea
151		tert-butyl (2r,4s)-2- (3-(4- chlorobenzyl)ureido)- 6- azaspiro[3.4]octane- 6-carboxylate
152		tert-butyl (2s,4r)-2- (3-(4- chlorobenzyl)ureido)- 6- azaspiro[3.4]octane- 6-carboxylate
153		1-(4- methoxybenzyl)-3- (2-(2-methyl-2-(p- tolyl)propanoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
154		1-(4- methoxybenzyl)-3- (2-(2-methyl-2-(m- tolyl)propanoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
155		1-(4-(2- methoxybenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
156		1-(2-(4- cyanobenzyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
157		1-(2-(4-(2- hydroxypropan-2- yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
158		1-(2-(4- chlorobenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
159		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(4- methylbenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
160		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(2- methylisonicotinyl)- 6- azaspiro[3.4]octan- 2-yl)urea
161		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(3- methylbenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
162		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(2- methylbenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
163		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(4- methoxybenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
164		1-(4-chlorobenzyl)- 3-((2s,4r)-6-(4- methylbenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
165		1-(4-chlorobenzyl)- 3-((2s,4r)-6-(4- methoxybenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
166		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(3- methylisonicotinoyl)- 6- azaspiro[3.4]octan- 2-yl)urea
167		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(4- fluorobenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
168		methyl 6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptane-2- carboxylate
169		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(3- isopropylbenzoyl)-6- azaspiro[3.4]octan- 2-yl)urea
170		1-(4-chlorobenzyl)- 3-((2s,4r)-6- (pyrimidin-2-yl)-6- azaspiro[3.4]octan- 2-yl)urea
171		1-(4-chlorobenzyl)- 3-((2r,5s)-6-(2- methylpyridin-4-yl)- 6- azaspiro[3.4]octan- 2-yl)urea
172		1-(2-(3- ethylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
173		1-(2-(3- isopropylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
174		1-(2-(3-(tert- butyl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
175		1-(2-(3-(2- hydroxypropan-2- yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
176		1-(2-(3- methoxybenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
177		1-(2-(3- hydroxybenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
178		1-(2-(3- (dimethylamino)ben- zoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
179		1-(4- methoxybenzyl)-3- (2-(3-(pyrrolidin-1- yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
180		1-(4- methoxybenzyl)-3- (2-(3- (methylsulfonyl)ben- zoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
181		methyl 3-(6-(3-(4- methoxybenzyl)urei- do)-2- azaspiro[3.3]heptane- 2- carbonyl)benzoate
182		1-(4-chlorobenzyl)- 3-((2R,4r,6R)-6-(4- (2-hydroxy-2- methylpropyl)pipera- zine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
183		1-(4-chlorobenzyl)- 3-((2r,4s)-6-(6- methylpyridin-2-yl)- 6- azaspiro[3.4]octan- 2-yl)urea
184		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)nicotinamide
185		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)isonicotinamide
186		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- methylisonicotinamide
187		1-(4-chlorobenzyl)- 3-((2S,4s,6S)-6-(4- (2-hydroxy-2- methylpropyl)pipera- zine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
188		1-(4- methoxybenzyl)-3- (2-(3-(2- oxopyrrolidin-1- yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
189		1-(2-(3-(1H-pyrrol- 1-yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- methoxybenzyl)urea
190		1-(4- methoxybenzyl)-3- (2-(3-(piperidin-1- yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
191		1-(4- methoxybenzyl)-3- (2-(3- morpholinobenzyl)- 2- azaspiro[3.3]heptan- 6-yl)urea
192		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-6- methylnicotinamide
193		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- methylbenzamide
194		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-3- methoxybenzamide
195		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-3- (methylsulfonyl)ben- zamide
196		1-(4-chlorobenzyl)- 3-(2-(2- phenoxyethoxy)ethyl) urea
197		tert-butyl 6-(3-(4- chlorobenzyl)ureido)- 2- azaspiro[3.3]heptane- 2-carboxylate
198		tert-butyl ((2R,4r,6R)-6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)carbamate
199		1-(4-chlorobenzyl)- 3-((2s,4r)-6-(4- methylpyridin-2-yl)- 6- azaspiro[3.4]octan- 2-yl)urea
200		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-3- hydroxybenzamide
201		methyl (2S,4s,6S)-6- (3-(4- chlorobenzyl)ureido) spiro[3.3]heptane-2- carboxylate
202		(2S,4s,6S)-6-(3-(4- chlorobenzyl)ureido)- N-methyl-N-((R)- tetrahydrofuran-3- yl)spiro[3.3]heptane- 2-carboxamide
203		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- methylnicotinamide
204		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-3- methylisonicotinamide
205		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-4- methylnicotinamide
206		1-(4-chlorobenzyl)- 3-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
207		1-(4-fluorobenzyl)- 3-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
208		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- hydroxybenzamide
209		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- (dimethylamino)ben- zamide
210		1-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(pyridin-4- ylmethyl)urea
211		4-((3-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
212		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-2- cyanobenzamide
213		N-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)pyridine-3- sulfonamdie
214		1-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-((6-oxo-1,6- dihydropyridin-3- yl)methyl)urea
215		5-((3-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)pic- olinamide
216		1-(4-chlorobenzyl)- 3-(2-((2- chlorophenyl)sulfonyl)- 2- azaspiro[3.3]heptan- 6-yl)urea
217		1-(4-chlorobenzyl)- 3-(2-((3- chlorophenyl)sulfonyl)- 2- azaspiro[3.3]heptan- 6-yl)urea
218		1-(4-chlorobenzyl)- 3-(2-((2- methoxyphenyl)sulfo- nyl)-2- azaspiro[3.3]heptan- 6-yl)urea
219		1-(2-(3-(1H-pyrrol- 1-yl)benzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(4- chlorobenzyl)urea
220		1-(4-chlorobenzyl)- 3-(2-(3- isopropylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
221		1-(4-chlorobenzyl)- 3-(2-(2-methyl-2- phenylpropanoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
222		4-((3-(2-(3- (pyrrolidin-1- yl)benzoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
223		4-((3-(2-(5- (pyrrolidin-1- yl)nicotinoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
224		4-((3-(2-(4- chlorobenzoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
225		4-((3-(2-(6- methylnicotinoyl)-2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
226		4-((3-(2-(2- methylisonicotinoyl)- 2- azaspiro[3.3]heptan- 6- yl)ureido)methyl)ben- zamide
227		1-((1H-pyrazol-4- yl)methyl)-3-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)urea
228		1-(2-(4- methylbenzoyl)-2- azaspiro[3.3]heptan- 6-yl)-3-(oxazol-4- ylmethyl)urea
229		1-(4- methoxybenzyl)-3- ((2S,4s,6S)-6- (1,2,3,4- tetrahydroquinoline- 1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
230		1-(4- methoxybenzyl)-3- (6-(4- methylpiperazine-1- carbonyl)spiro[3.3]hep- tan-2-yl)urea
231		methyl 4-(6-(3-(4- methoxybenzyl)urei- do)spiro[3.3]heptane- 2- carbonyl)piperazine- 1-carboxylate
232		1-(6-(1,1- dioxidothiomorpholine- 4- carbonyl)spiro[3.3]hep- tan-2-yl)-3-(4- methoxybenzyl)urea
233		methyl 4-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptane-2- carbonyl)piperazine- 1-carboxylate
234		1-(4-chlorobenzyl)- 3-(6-(2-(4-(2- hydroxy-2- methylpropyl)pipera- zin-1-yl)-2- oxoethyl)spiro[3.3]h
235		(S)-1-(4- chlorobenzyl)-3-(6- (2-(2- (hydroxymethyl)pyrro- lidin-1-yl)-1- oxoethyl)spiro[3.3]hep- tan-2-yl)urea
236		1-(4-chlorobenzyl)- 3-(6-(2-oxo-2- (pyrrolidin-1- yl)ethyl)spiro[3.3]hep- tan-2-yl)urea
237		N-benzyl-2-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)-N- methylpropanamide
238		1-(4-chlorobenzyl)- 3-(6-((4-methyl-3- oxopiperazin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
239		(R)-1-(4- chlorobenzyl)-3-(6- ((2-(pyridin-3- yl)pyrrolidin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
240		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-6- methylnicotinamide
241		1-(4-chlorobenzyl)- 3-(6-((2-methyl-5- oxopyrrolidin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
242		1-(4-chlorobenzyl)- 3-(6-((5-phenyl-1H- 1,2,3-triazol-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
243		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)tetrahydro- 2H-thiopyran-4- carboxamide 1,1- dioxide
244		1-(4-chlorobenzyl)- 3-(6-((3-methyl-2- oxopyrrolidin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
245		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-6- methylpicolinamide
246		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-2- methylisonicotinamide
247		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-1H- pyrazole-4- carboxamide
248		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-N,6- dimethylnicotinamide
249		N-((2R,4r,6R)-6-(3- (4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-6- methylnicotinamide
250		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)tetrahydro- 2H-pyran-4- carboxamide
251		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)cyclopentane- carboxamide
252		N-((6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)methyl)-2- oxopiperidine-4- carboxamide
253		1-(4-chlorobenzyl)- 3-(6-(1-(4-methyl-3- oxopiperazin-1- yl)ethyl)spiro[3.3]hep- tan-2-yl)urea
254		1-(4-chlorobenzyl)- 3-(6-((4-methyl-2- phenylpiperazin-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
255		N-(1-(6-(3-(4- chlorobenzyl)ureido) spiro[3.3]heptan-2- yl)ethyl)-6- methylnicotinamide
256		1-(4-chlorobenzyl)- 3-(5-(3,4- dihydroquinolin- 1(2H)-yl)-5- oxopentyl)urea
257		6-(3-(4- chlorobenzyl)ureido)- N- cyclohexylhexanamide
258		6-(3-(4- chlorobenzyl)ureido)- N- cylcopentylhexanamide
259		1-(4-chlorobenzyl)- 3-(6-morpholino-6- oxohexyl)urea
260		1-(4-chlorobenzyl)- 3-(6-(4- neopentylpiperazin- 1-yl)-6- oxohexyl)urea
261		1-(4-chlorobenzyl)- 3-(6-(4-(2-hydroxy- 2- methylpropyl)pipera- zin-1-yl)-6- oxohexyl)urea
262		6-(3-(4- chlorobenzyl)ureido)- N-(o- tolyl)hexanamide
263		6-(3-(4- chlorobenzyl)ureido)- N-(pyridin-4- yl)hexanamide
264		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N-(m- tolyl)hexanamide
265		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N- (pyridin-4- yl)hexanamide
266		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N-(o- tolyl)hexanamide
267		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N-(3- methylbenzyl)hexan- amide
268		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N- phenylhexanamide
269		N-benzyl-6-(3-(4- chlorobenzyl)ureido)- N- methylhexanamide
270		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N- (pyridin-3- yl)hexanamide
271		6-(3-(4- chlorobenzyl)ureido)- N-methyl-N- (pyridin-2- yl)hexanamide
272		6-(3-(4- chlorobenzyl)ureido)- N-(2- fluorophenyl)hexana- mide
273		N-([1,1′-biphenyl]- 2-yl)-6-(3-(4- chlorobenzyl)ureido) hexanamide
274		6-(3-(4- chlorobenzyl)ureido)- N-(2-fluorophenyl)- N- methylhexanamide
275		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)-2- methylbenzamide
276		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)-3- methylbenzamide
277		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)nicotinamide
278		6-(3-(4- chlorobenzyl)ureido)- N-(6- methylpyridin-3- yl)hexanamide
279		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)picolinamide
280		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)-2- fluorobenzamide
281		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)-6- methylnicotinamide
282		N-(2-fluorophenyl)- 6-(3-(4- methoxybenzyl)urei- do)-N- methylhexanamide
283		N-(5-(3-(4- chlorobenzyl)ureido) pentyl)-2-(pyridin-3- yl)acetamide
284		6-(3-(4- chlorobenzyl)ureido)- N-(4- fluorophenyl)hexana- mide
285		6-(3-(4- chlorobenzyl)ureido)- N-(3- fluorophenyl)hexana- mide
286		N-(2-fluorophenyl)- N-methyl-6-(3- (pyridin-4- ylmethyl)ureido)hex- anamide
287		6-(3-((1H-pyrazol-4- yl)methyl)ureido)- N-(2-fluorophenyl)- N- methylhexanamide
288		N-(2-fluorophenyl)- N-methyl-6-(3- (oxazol-5- ylmethyl)ureido)hex- anamide
289		1-(4-chlorobenzyl)- 3-(4-(1- nicotinoylpiperidin- 4-yl)butyl)urea
290		1-(4-chlorobenzyl)- 3-(4-(1- isonicotinoyl)piperidin- 4-yl)butyl)urea
291		1-(4-chlorobenzyl)- 3-(4-(1-(2- phenylacetyl)piperidin- 4-yl)butyl)urea
292		1-(4-chlorobenzyl)- 3-(4-(1- picolinylpiperidin- 4-yl)butyl)urea
293		1-(4-(1- benzoylpiperidin-4- yl)butyl-1,1-d2)-3- (oxazol-5- ylmethyl)urea
294		1-(4-chlorobenzyl)- 3-(4-(1-(2-(pyridin- 3- yl)acetyl)piperidin- 4-yl)butyl)urea
295		1-(4-chlorobenzyl)- 3-(4-(1-(2-(pyridin- 4- yl)acetyl)piperidin- 4-yl)butyl)urea
296		1-(4-chlorobenzyl)- 3-(4-(1-(3- methylbenzoyl)piper- idin-4-yl)butyl)urea
297		1-(4-chlorobenzyl)- 3-(4-(1-(2- methylbenzoyl)piper- idin-4-yl)butyl)urea
298		1-(4-chlorobenzyl)- 3-(4-(1-(6- methylpicolinyl)piper- idin-4- yl)butyl)urea
299		1-(4-chlorobenzyl)- 3-(4-(1-(2-(6- methylpyridin-2- yl)acetyl)piperidin- 4-yl)butyl)urea
300		1-(4-chlorobenzyl)- 3-(4-(1-(tetrahydro- 2H-pyran-4- carbonyl)piperidin- 4-yl)butyl)urea
301		1-(4-chlorobenzyl)- 3-(4-(1-(2- oxopiperidine-4- carbonyl)piperidin- 4-yl)butyl)urea
302		1-(4-chlorobenzyl)- 3-(4-(1-(1-methyl-2- oxopiperidine-4- carobnyl)piperidin- 4-yl)butyl)urea
303		1-(4-chlorobenzyl)- 3-(4-(1-(5- oxopyrrolidine-3- carbonyl)piperidin- 4-yl)butyl)urea
304		1-(4-chlorobenzyl)- 3-(4-(1-(1-methyl-5- oxopyrrolidine-3- carbonyl)piperidin- 4-yl)butyl)urea
305		1-(4-chlorobenzyl)- 3-(4-(1-(oxazole-2- carbonyl)piperidin- 4-yl)butyl)urea
306		1-(4-chlorobenzyl)- 3-(4-(1-(isoxazole-5- carbonyl)piperidin- 4-l)butyl)urea
307		1-(4-chlorobenzyl)- 3-(4-(1-(pyridin-2- yl)piperidin-4- yl)butyl)urea
308		1-(4-chlorobenzyl)- 3-(4-(1-(pyridin-4- yl)piperidin-4- yl)butyl)urea
309		1-(4-chlorobenzyl)- 3-(4-(1-(6- methylnicotinoyl)piper- idin-4- yl)butyl)urea
310		1-(4-chlorobenzyl)- 3-(4-(1-(2-(2- methylpyridin-3- yl)acetyl)piperidin- 4-yl)butyl)urea
311		1-(4-chlorobenzyl)- 3-(4-(1-(2-(6- methylpyridin-3- yl)acetyl)piperidin- 4-yl)butyl)urea
312		1-(4-chlorobenzyl)- 3-(4-(1-(1-methyl- 1H-1,2,3-triazole-4- carbonyl)piperidin- 4-yl)butyl)urea
313		1-(4-chlorobenzyl)- 3-(4-(1-(2-(o- tolyl)acetyl)piperidin- 4-yl)butyl)urea
314		1-(4-chlorobenzyl)- 3-(4-(1-(2- (difluoromethyl)ben- zoyl)piperidin-4- yl)butyl)urea
315		1-(4-(1-(2-(1H- tetrazol-5- yl)benzoyl)piperidin- 4-yl)butyl)-3-(4- chlorobenzyl)urea
316		1-(4-(1-(2-(1H- pyrazol-4- yl)acetyl)piperidin- 4-yl)butyl)-3-(4- chlorobenzyl)urea
317		1-(4-(4- benzoylpiperazin-1- yl)butyl)-3-(4- chlorobenzyl)urea
318		1-(4-(1-(2H-tetrazol- 5-yl)piperidin-4- yl)butyl)-3-(4- chlorobenzyl)urea
319		1-(4-chlorobenzyl)- 3-(4-(1-(2,6- dimethylbenzoyl)piper- idin-4- yl)butyl)urea
320		1-(4-(1-(2- methylbenzoyl)piper- idin-4-yl)butyl)-3- (oxazol-5- ylmethyl)urea
321		4-((3-(4-(1-(2- methylbenzoyl)piper- idin-4- yl)butyl)ureido)meth- yl)benzamide
322		1-(4- methoxybenzyl)-3- (4-(1-(2- methylbenzoyl)piper- idin-4-yl)butyl)urea
323		1-(4-(1-(2- methylbenzoyl)piper- idin-4-yl)butyl)-3- (pyridin-4- ylmethyl)urea
324		1-(4-(1- benzoylpiperidin-4- yl)butyl)-3-(oxazol- 5-ylmethyl-d2)urea
325		1-(4- methoxybenzyl)-3- (6-(5-phenyl-1,3,4- oxadiazol-2- yl)spiro[3.3]heptan- 2-yl)urea
326		1-(4- methoxybenzyl)-3- (6-(4-phenyloxazol- 2- yl)spiro[3.3]heptan- 2-yl)urea
327		1-(6- (benzo[d]oxazol-2- yl)spiro[3.3]heptan- 2-yl)-3-(4- methoxybenzyl)urea
328		1-(4-chlorobenzyl)- 3-(6- (hydroxy(phenyl)meth- yl)spiro[3.3]heptan- 2-yl)urea
329		1-(4-chlorobenzyl)- 3-(6-(pyridin-4- ylmethyl)spiro[3.3]hep- tan-2-yl)urea
330		1-(4- methoxybenzyl)-3- (6-(pyridin-4- ylmethyl)spiro[3.3]hep- tan-2-yl)urea
331		1-(4-chlorobenzyl)- 3-(6-(pyrazin-2- ylmethyl)spiro[3.3]hep- tan-2-yl)urea
332		1-(4- methoxybenzyl)-3- (6-(5-(6- methylpyridin-3-yl)- 1,3,4-oxadiazol-2- yl)spiro[3.3]heptan- 2-yl)urea
333		1-(4-chlorobenzyl)- 3-(6-((4-cyano-1H- pyrazol-1- yl)methyl)spiro[3.3] heptan-2-yl)urea
334		1-(4- methoxybenzyl)-3- (6-(4- methylbenzyl)spiro[3.3] heptan-2-yl)urea
335		1-(4- methoxybenzyl)-3- (6-(3- methylbenzoyl)spiro[3.3] heptan-2-y)urea
336		1-(4- methoxybenzyl)-3- (6-(2- methylbenzyl)spiro[3.3] heptan-2-yl)urea
337		1-(4- methoxybenzyl)-3- (6-((6- methylpyridin-3- yl)methyl)spiro[3.3] heptan-2-yl)urea
338		1-(4-chlorobenzyl)- 3-(6-(1-hydroxy-1- (6-methylpyridin-3- yl)ethyl)spiro[3.3]hep- tan-2-yl)urea
339		1-(6-((1H-1,2,4- triazol-1- yl)methyl)spiro[3.3] heptan-2-yl)-3-(4- chlorobenzyl)urea
340		1-(4-chlorobenzyl)- 3-(6-(pyrimidin-2- ylmethyl)spiro[3.3]hep- tan-2-yl)urea
341		1-(4-chlorobenzyl)- 3-(6-(pyridin-4- yloxy)spiro[3.3]heptan- 2-yl)urea
342		1-(4-chlorobenzyl)- 3-(6- (methylsulfonyl)spiro [3.3]heptan-2- yl)urea
343		1-(4-chlorobenzyl)- 3-(6-(pyridin-3- yloxy)spiro[3.3]heptan- 2-yl)urea
344		1-(4- methoxybenzyl)-3- (6-(pyridin-3- yloxy)spiro[3.3]heptan- 2-yl)urea
345		1-(4-chlorobenzyl)- 3-(6-(pyiridin-3- ylmethyl)spiro[3.3]hep- tan-2-yl)urea
346		1-(4-chlorobenzyl)- 3-(6-((2- methylpyridin-3- yl)methyl)spiro[3.3] heptan-2-yl)urea
347		1-(4-chlorobenzyl)- 3-(6-((6- methylpyridin-3- yl)methyl)spiro[3.3] heptan-2-yl)urea
348		1-(4-chlorobenzyl)- 3-(6-(pyridin-4- ylmethoxy)spiro[3.3] heptan-2-yl)urea
349		1-(4- methoxybenzyl)-3- (6-(pyridin-4- ylmethoxy)spiro[3.3] heptan-2-yl)urea
350		1-(4-chlorobenzyl)- 3-(6-(pyridin-3- ylmethoxy)spiro[3.3] heptan-2-yl)urea
351		1-(4- methoxybenzyl)-3- (6-(pyridin-3- ylmethoxy)spiro[3.3] heptan-2-yl)urea
352		1-(4-chlorobenzyl)- 3-(6- ((phenylsulfonyl)meth- yl)spiro[3.3]heptan- 2-yl)urea
353		1-(4-chlorobenzyl)- 3-(6-((pyridin-3- ylsulfonyl)methyl)spi- ro[3.3]heptan-2- yl)urea
354		1-((2r,4s)-6-([1,4′- bipiperidine]-1′- carbonyl)-6- azaspiro[3.4]octan- 2-yl)-3-(4- chlorobenzyl)urea
indicates data missing or illegible when filed

In some embodiments, provided herein is a compound of Formula (II), or any variation thereof, or a pharmaceutically acceptable salt of any of the foregoing, selected from the group consisting of:

• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-4-ylmethyl)urea; tert-butyl (6-(3-(4-carbamoylbenzyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• 4-((3-(4,4-dimethylcyclohexyl)ureido)methyl)benzamide;
• 4-((3-(3-phenylcyclobutyl)ureido)methyl)benzamide;
• tert-butyl 4-(3-(4-carbamoylbenzyl)ureido)piperidine-1-carboxylate;
• tert-butyl (6-(3-(pyridin-4-ylmethyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• tert-butyl (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• tert-butyl (6-(3-(4-(hydroxymethyl)benzyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• tert-butyl (6-(3-((1H-pyrazol-4-yl)methyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• tert-butyl (6-(3-(oxazol-5-ylmethyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• tert-butyl (4-(3-(4-carbamoylbenzyl)ureido)cyclohexyl)carbamate;
• 4-((3-(1-benzoylpiperidin-4-yl)ureido)methyl)benzamide;
• N-(6-(3-(4-carbamoylbenzyl)ureido)spiro[3.3]heptan-2-yl)benzamide;
• N-(6-(3-(pyridin-4-ylmethyl)ureido)spiro[3.3]heptan-2-yl)benzamide;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea;
• N-(6-(3-((1H-pyrazol-4-yl)methyl)ureido)spiro[3.3]heptan-2-yl)benzamide;
• N-(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)benzamide;
• 4-((3-(4-(1-benzoylpiperidin-4-yl)butyl)ureido)methyl)benzamide;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-methoxybenzyl)urea;
• 4-((3-(3-(benzylcarbamoyl)cyclobutyl)ureido)methyl)benzamide;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-(hydroxymethyl)benzyl)urea;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(oxazol-5-ylmethyl)urea;
• 4-((3-(6-(benzylamino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide;
• tert-butyl 1-((3-(pyridin-4-ylmethyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• 4-((3-(6-(pyridin-2-ylamino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide;
• tert-butyl 1-((3-(4-chlorobenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-(4-methoxybenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-(4-(hydroxymethyl)benzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-(oxazol-5-ylmethyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-((1H-pyrazol-4-yl)methyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-(4-acetamidobenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• tert-butyl 1-((3-(4-carbamoylbenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate;
• 4-((3-(6-((pyridin-2-ylmethyl)amino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide; methyl 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylate;
• tert-butyl (5-(3-(4-methoxybenzyl)ureido)pentyl)carbamate;
• tert-butyl 6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxylate;
• 1-(2-(2-(2-fluorophenyl)acetyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(2-(2-chlorophenyl)acetyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-(2-methoxyphenyl)acetyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-(2-(trifluoromethyl)phenyl)acetyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-(o-tolyl)acetyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 6-(3-(4-methoxybenzyl)ureido)-N-(1-phenylcyclopropyl)spiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-(2-phenylpyrrolidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 6-(3-(4-methoxybenzyl)ureido)-N-(1-phenylethyl)spiro[3.3]heptane-2-carboxamide;
• N-(2-hydroxy-1-phenylethyl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-(2-phenylazetidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-3-ylmethyl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-4-ylmethyl)spiro[3.3]heptane-2-carboxamide;
• N-benzyl-6-(3-(4-methoxybenzyl)ureido)-N-methylspiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-((2-phenylpyrrolidin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• N-(1-(2-fluorophenyl)ethyl)-6-(3-(4-methoxybenzyl)ureido)-N-methylspiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-(o-tolyl)propyl)spiro[3.3]heptane-2-carboxamide;
• N-(2-(2-fluorophenyl)-2-methylpropyl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-2-ylmethyl)spiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-(3-phenylpyrrolidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(2-(pyridin-4-yl)pyrrolidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(2-(pyridin-3-yl)pyrrolidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(3-phenylazetidine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(4-benzoylpiperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 6-(3-(4-methoxybenzyl)ureido)-N-(3-phenylcyclobutyl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-(2-methoxyphenyl)-2-methylpropyl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-(pyridin-2-yl)propyl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-(pyridin-3-yl)propyl)spiro[3.3]heptane-2-carboxamide;
• N-benzyl-2-(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)-N-methylacetamide;
• N-benzyl-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-phenethylspiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-phenylpropan-2-yl)spiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-(1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(7-(trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(isoindoline-2-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(indoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• N-(2-(1H-pyrazol-4-yl)ethyl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 1-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• N-(4-cyano-2-fluorobenzyl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(3-(pyridin-4-yl)cyclobutyl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-methyl-N-(tetrahydrofuran-3-yl)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-(pyridin-4-yl)propyl)spiro[3.3]heptane-2-carboxamide;
• tert-butyl 2-(3-(4-methoxybenzyl)ureido)-6-azaspiro[3.4]octane-6-carboxylate;
• tert-butyl 6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.4]octane-2-carboxylate;
• 1-(4-methoxybenzyl)-3-(6-(6-methyl-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(3,4-dihydro-2H-benzo[b][1,4]oxazine-4-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 6-(3-(4-methoxybenzyl)ureido)-N-phenylspiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-methyl-N-phenylspiro[3.3]heptane-2-carboxamide;
• N-((2-(difluoromethoxy)pyridin-4-yl)methyl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• N-([1,2,4]triazolo[4,3-a]pyridin-6-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 1-(4-methoxybenzyl)-3-(6-(1,2,3,4-tetrahydro-1,6-naphthyridine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• N-(2,3-dihydro-1H-inden-1-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• N-(3-(hydroxymethyl)-2,3-dihydro-1H-inden-1-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• N-(1-hydroxy-2,3-dihydro-1H-inden-2-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• N-(2,3-dihydro-1H-inden-2-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(1,2,3,4-tetrahydronaphthalen-2-yl)spiro[3.3]heptane-2-carboxamide;
• N-(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• N-(6-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)spiro[3.3]heptane-2-carboxamide;
• 1-(6-(6-fluoro-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(7,8-difluoro-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(6-(difluoromethoxy)-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(6-(6-(trifluoromethyl)-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(5-fluoro-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(7-fluoro-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(6-(6-(trifluoromethoxy)-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(7-methyl-1,2,3,4-tetrahydroquinoline-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-fluorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-(oxetan-3-yl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(4-(cyclopropylmethyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(2-(hydroxymethyl)-4-methylpiperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)benzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-phenylacetamide;
• 1-(2-((2-chlorophenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-((2-chlorobenzyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-((2-chlorophenethyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(dibenzylamino)spiro[3.3]heptan-2-yl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-1-(2-chlorophenyl)methanesulfonamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)benzenesulfonamide;
• 1-(6-(4-isopropylpiperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-((1-methyl-1H-pyrazol-4-yl)methyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-(pyridin-4-ylmethyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-(pyridin-2-ylmethyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(3-(hydroxymethyl)-4-methylpiperazine-1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-((5,7-difluoro-3,4-dihydroquinolin-1(2H)-yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(indolin-1-ylmethyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(6-(isoindolin-2-ylmethyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(bicyclo[2.2.1]heptan-2-ylsulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• methyl 4-((6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptan-2-yl)sulfonyl)cyclohexane-1-carboxylate;
• N-(6-cyanopyridin-2-yl)-6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxamide;
• 6-(3-(4-methoxybenzyl)ureido)-N-(2-methylpyrimidin-5-yl)-2-azaspiro[3.3]heptane-2-carboxamide;
• 1-(6-((1H-indazol-1-yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-(2-chlorophenyl)propanoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• tert-butyl 3-(6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carbonyl)piperidine-1-carboxylate;
• 1-(4-methoxybenzyl)-3-(2-(1,2,3,4-tetrahydronaphthalene-1-carbonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(6-methylnicotinoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-isonicotinoyl-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-methylisonicotinoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-benzoyl-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-methyl-2-phenylpropanoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(1-phenylcyclopropane-1-carbonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(1-methyl-6-oxo-1,6-dihydropyridine-3-carbonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(3-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(4-(trifluoromethyl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(5-phenoxypentyl)urea;
• 1-(4-methoxybenzyl)-3-(6-phenoxyhexyl)urea;
• tert-butyl 2-(3-(4-chlorobenzyl)ureido)-6-azaspiro[3.4]octane-6-carboxylate;
• 1-(4-methoxybenzyl)-3-(2-(2-methyl-2-(p-tolyl)propanoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(2-methyl-2-(m-tolyl)propanoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-(4-methoxybenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(4-cyanobenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(4-(2-hydroxypropan-2-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(4-chlorobenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(4-methylbenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(2-methylisonicotinoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(3-methylbenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(2-methylbenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(4-methoxybenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(3-methylisonicotinoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(4-fluorobenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(3-isopropylbenzoyl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyrimidin-2-yl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(2-methylpyridin-4-yl)-6-azaspiro[3.4]octan-2-yl)urea;
• 1-(2-(3-ethylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-isopropylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-(tert-butyl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-(2-hydroxypropan-2-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-methoxybenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-hydroxybenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(2-(3-(dimethylamino)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(2-(3-(pyrrolidin-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(3-(methylsulfonyl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• methyl 3-(6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carbonyl)benzoate;
• 1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)nicotinamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)isonicotinamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-methylisonicotinamide;
• 1-(4-methoxybenzyl)-3-(2-(3-(2-oxopyrrolidin-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-(3-(1H-pyrrol-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-methoxybenzyl)-3-(2-(3-(piperidin-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-methoxybenzyl)-3-(2-(3-morpholinobenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-6-methylnicotinamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-methylbenzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-3-methoxybenzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-3-(methylsulfonyl)benzamide;
• 1-(4-chlorobenzyl)-3-(2-(2-phenoxyethoxy)ethyl)urea;
• tert-butyl 6-(3-(4-chlorobenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxylate;
• tert-butyl (6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)carbamate;
• 1-(4-chlorobenzyl)-3-(6-(6-methylpyridin-2-yl)-6-azaspiro[3.4]octan-2-yl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-3-hydroxybenzamide;
• methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylate;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(tetrahydrofuran-3-yl)spiro[3.3]heptane-2-carboxamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-methylnicotinamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-3-methylisonicotinamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-4-methylnicotinamide;
• 1-(4-chlorobenzyl)-3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-fluorobenzyl)-3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-hydroxybenzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-(dimethylamino)benzamide;
• 1-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(pyridin-4-ylmethyl)urea;
• 4-((3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-2-cyanobenzamide;
• N-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)pyridine-3-sulfonamide;
• 1-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-((6-oxo-1,6-dihydropyridin-3-yl)methyl)urea;
• 5-((3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)picolinamide;
• 1-(4-chlorobenzyl)-3-(2-((2-chlorophenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-chlorobenzyl)-3-(2-((3-chlorophenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-chlorobenzyl)-3-(2-((2-methoxyphenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-(3-(1H-pyrrol-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-chlorobenzyl)urea;
• 1-(4-chlorobenzyl)-3-(2-(3-isopropylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(4-chlorobenzyl)-3-(2-(2-methyl-2-phenylpropanoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 4-((3-(2-(3-(pyrrolidin-1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• 4-((3-(2-(5-(pyrrolidin-1-yl)nicotinoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• 4-((3-(2-(4-chlorobenzoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• 4-((3-(2-(6-methylnicotinoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• 4-((3-(2-(2-methylisonicotinoyl)-2-azaspiro[3.3]heptan-6-yl)ureido)methyl)benzamide;
• 1-((1H-pyrazol-4-yl)methyl)-3-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)urea;
• 1-(2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(oxazol-4-ylmethyl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-methylpiperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea;
• methyl 4-(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carbonyl)piperazine-1-carboxylate;
• 1-(6-(1,1-dioxidothiomorpholine-4-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• methyl 4-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carbonyl)piperazine-1-carboxylate;
• 1-(4-chlorobenzyl)-3-(6-(2-(4-(2-hydroxy-2-methylpropyl)piperazin-1-yl)-2-oxoethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)-2-oxoethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(2-oxo-2-(pyrrolidin-1-yl)ethyl)spiro[3.3]heptan-2-yl)urea;
• N-benzyl-2-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-N-methylpropanamide;
• 1-(4-chlorobenzyl)-3-(6-((4-methyl-3-oxopiperazin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((2-(pyridin-3-yl)pyrrolidin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((2-methyl-5-oxopyrrolidin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((5-phenyl-1H-1,2,3-triazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)tetrahydro-2H-thiopyran-4-carboxamide 1,1-dioxide;
• 1-(4-chlorobenzyl)-3-(6-((3-methyl-2-oxopyrrolidin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-6-methylpicolinamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-2-methylisonicotinamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-1H-pyrazole-4-carboxamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-N,6-dimethylnicotinamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-6-methylnicotinamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)tetrahydro-2H-pyran-4-carboxamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)cyclopentanecarboxamide;
• N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)-2-oxopiperidine-4-carboxamide;
• 1-(4-chlorobenzyl)-3-(6-(1-(4-methyl-3-oxopiperazin-1-yl)ethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((4-methyl-2-phenylpiperazin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• N-(1-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)ethyl)-6-methylnicotinamide;
• 1-(4-chlorobenzyl)-3-(5-(3,4-dihydroquinolin-1(2H)-yl)-5-oxopentyl)urea;
• 6-(3-(4-chlorobenzyl)ureido)-N-cyclohexylhexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-cyclopentylhexanamide;
• 1-(4-chlorobenzyl)-3-(6-morpholino-6-oxohexyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(4-neopentylpiperazin-1-yl)-6-oxohexyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazin-1-yl)-6-oxohexyl)urea;
• 6-(3-(4-chlorobenzyl)ureido)-N-(o-tolyl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(pyridin-4-yl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(m-tolyl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(pyridin-4-yl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(o-tolyl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(3-methylbenzyl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-phenylhexanamide;
• N-benzyl-6-(3-(4-chlorobenzyl)ureido)-N-methylhexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(pyridin-3-yl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(pyridin-2-yl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(2-fluorophenyl)hexanamide;
• N-([1,1′-biphenyl]-2-yl)-6-(3-(4-chlorobenzyl)ureido)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(2-fluorophenyl)-N-methylhexanamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-2-methylbenzamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-3-methylbenzamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)nicotinamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(6-methylpyridin-3-yl)hexanamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)picolinamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-2-fluorobenzamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-6-methylnicotinamide;
• N-(2-fluorophenyl)-6-(3-(4-methoxybenzyl)ureido)-N-methylhexanamide;
• N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-2-(pyridin-3-yl)acetamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(4-fluorophenyl)hexanamide;
• 6-(3-(4-chlorobenzyl)ureido)-N-(3-fluorophenyl)hexanamide;
• N-(2-fluorophenyl)-N-methyl-6-(3-(pyridin-4-ylmethyl)ureido)hexanamide;
• 6-(3-((1H-pyrazol-4-yl)methyl)ureido)-N-(2-fluorophenyl)-N-methylhexanamide;
• N-(2-fluorophenyl)-N-methyl-6-(3-(oxazol-5-ylmethyl)ureido)hexanamide;
• 1-(4-chlorobenzyl)-3-(4-(1-nicotinoylpiperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-isonicotinoylpiperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-phenylacetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-picolinoylpiperidin-4-yl)butyl)urea;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl-1,1-d2)-3-(oxazol-5-ylmethyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(pyridin-3-yl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(pyridin-4-yl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(3-methylbenzoyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-methylbenzoyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(6-methylpicolinoyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(6-methylpyridin-2-yl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(tetrahydro-2H-pyran-4-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-oxopiperidine-4-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-2-oxopiperidine-4-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(5-oxopyrrolidine-3-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-5-oxopyrrolidine-3-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(oxazole-2-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(isoxazole-5-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(pyridin-2-yl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(pyridin-4-yl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(6-methylnicotinoyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(2-methylpyridin-3-yl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(6-methylpyridin-3-yl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-1H-1,2,3-triazole-4-carbonyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(o-tolyl)acetyl)piperidin-4-yl)butyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2-(difluoromethyl)benzoyl)piperidin-4-yl)butyl)urea;
• 1-(4-(1-(2-(1H-tetrazol-5-yl)benzoyl)piperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea;
• 1-(4-(1-(2-(1H-pyrazol-4-yl)acetyl)piperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea;
• 1-(4-(4-benzoylpiperazin-1-yl)butyl)-3-(4-chlorobenzyl)urea;
• 1-(4-(1-(2H-tetrazol-5-yl)piperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea;
• 1-(4-chlorobenzyl)-3-(4-(1-(2,6-dimethylbenzoyl)piperidin-4-yl)butyl)urea;
• 1-(4-(1-(2-methylbenzoyl)piperidin-4-yl)butyl)-3-(oxazol-5-ylmethyl)urea;
• 4-((3-(4-(1-(2-methylbenzoyl)piperidin-4-yl)butyl)ureido)methyl)benzamide;
• 1-(4-methoxybenzyl)-3-(4-(1-(2-methylbenzoyl)piperidin-4-yl)butyl)urea;
• 1-(4-(1-(2-methylbenzoyl)piperidin-4-yl)butyl)-3-(pyridin-4-ylmethyl)urea;
• 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(oxazol-5-ylmethyl-d2)urea;
• 1-(4-methoxybenzyl)-3-(6-(5-phenyl-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-phenyloxazol-2-yl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-(benzo[d]oxazol-2-yl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(hydroxy(phenyl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyrazin-2-ylmethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((4-cyano-1H-pyrazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(4-methylbenzyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(3-methylbenzyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(2-methylbenzyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-((6-methylpyridin-3-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(1-hydroxy-1-(6-methylpyridin-3-yl)ethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(6-((1H-1,2,4-triazol-1-yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-4-yloxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(methylsulfonyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-3-yloxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(pyridin-3-yloxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-3-ylmethyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((2-methylpyridin-3-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((6-methylpyridin-3-yl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-(pyridin-3-ylmethoxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-methoxybenzyl)-3-(6-(pyridin-3-ylmethoxy)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((phenylsulfonyl)methyl)spiro[3.3]heptan-2-yl)urea;
• 1-(4-chlorobenzyl)-3-(6-((pyridin-3-ylsulfonyl)methyl)spiro[3.3]heptan-2-yl)urea; and
• 1-(6-([1,4′-bipiperidine]-1′-carbonyl)-6-azaspiro[3.4]octan-2-yl)-3-(4-chlorobenzyl)urea,or a pharmaceutically acceptable salt of any of the foregoing.

In some variations, any of the compounds described herein, such as a compound of Formula (I) or Formula (II), or any variation thereof, or a compound of Table 1 may be deuterated (e.g., a hydrogen atom is replaced by a deuterium atom). In some of these variations, the compound is deuterated at a single site. In other variations, the compound is deuterated at multiple sites. Deuterated compounds can be prepared from deuterated starting materials in a manner similar to the preparation of the corresponding non-deuterated compounds. Hydrogen atoms may also be replaced with deuterium atoms using other method known in the art.

Any formula given herein, such as Formula (II), (I) (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), is intended to represent compounds having structures depicted by the structural formula as well as certain variations or forms. In particular, compounds of any formula given herein may have asymmetric centers and therefore exist in different enantiomeric or diastereomeric forms. All optical isomers and stereoisomers of the compounds of the general formula, and mixtures thereof in any ratio, are considered within the scope of the formula. Thus, any formula given herein is intended to represent a racemate, one or more enantiomeric forms, one or more diastereomeric forms, one or more atropisomeric forms, and mixtures thereof in any ratio. Where a compound of Table 1 is depicted with a particular stereochemical configuration, also provided herein is any alternative stereochemical configuration of the compound, as well as a mixture of stereoisomers of the compound in any ratio. For example, where a compound of Table 1 has a stereocenter that is in an “S” stereochemical configuration, also provided herein is enantiomer of the compound wherein that stereocenter is in an “R” stereochemical configuration. Likewise, when a compound of Table 1 has a stereocenter that is in an “R” configuration, also provided herein is enantiomer of the compound in an “S” stereochemical configuration. Also provided are mixtures of the compound with both the “S” and the “R” stereochemical configuration. Additionally, if a compound of Table 1 has two or more stereocenters, also provided are any enantiomer or diastereomer of the compound. For example, if a compound of Table 1 contains a first stereocenter and a second stereocenter with “R” and “R” stereochemical configurations, respectively, also provided are stereoisomers of the compound having first and second stereocenters with “S” and “S” stereochemical configurations, respectively, “S” and “R” stereochemical configurations, respectively, and “R” and “S” stereochemical configurations, respectively. If a compound of Table 1 contains a first stereocenter and a second stereocenter with “S” and “S” stereochemical configurations, respectively, also provided are stereoisomers of the compound having first and second stereocenters with “R” and “R” stereochemical configurations, respectively, “S” and “R” stereochemical configurations, respectively, and “R” and “S” stereochemical configurations, respectively. If a compound of Table 1 contains a first stereocenter and a second stereocenter with “S” and “R” stereochemical configurations, respectively, also provided are stereoisomers of the compound having first and second stereocenters with “R” and “S” stereochemical configurations, respectively, “R” and “R” stereochemical configurations, respectively, and “S” and “S” stereochemical configurations, respectively. Similarly, if a compound of Table 1 contains a first stereocenter and a second stereocenter with “R” and “S” stereochemical configurations, respectively, also provided are stereoisomers of the compound having first and second stereocenters with “S” and “R” stereochemical configurations, respectively, “R” and “R” stereochemical configurations, respectively, and “S” and “S” stereochemical configurations, respectively. Furthermore, certain structures may exist as geometric isomers (i.e., cis and trans isomers), as tautomers, or as atropisomers. Additionally, any formula given herein is intended to refer also to any one of hydrates, solvates, and amorphous and polymorphic forms of such compounds, and mixtures thereof, even if such forms are not listed explicitly. In some embodiments, the solvent is water and the solvates are hydrates.

Representative examples of compounds detailed herein, including intermediates and final compounds, are depicted in the tables and elsewhere herein. It is understood that in one aspect, any of the compounds may be used in the methods detailed herein, including, where applicable, intermediate compounds that may be isolated and administered to an individual or subject.

The compounds depicted herein may be present as salts even if salts are not depicted, and it is understood that the compositions and methods provided herein embrace all salts and solvates of the compounds depicted here, as well as the non-salt and non-solvate form of the compound, as is well understood by the skilled artisan. In some embodiments, the salts of the compounds provided herein are pharmaceutically acceptable salts.

In one variation, the compounds herein are synthetic compounds prepared for administration to an individual or subject. In another variation, compositions are provided containing a compound in substantially pure form. In another variation, provided are pharmaceutical compositions comprising a compound detailed herein and a pharmaceutically acceptable carrier. In another variation, methods of administering a compound are provided. The purified forms, pharmaceutical compositions and methods of administering the compounds are suitable for any compound or form thereof detailed herein.

Any variation or embodiment of R^a, R^b, R^q, R^s, R^t, R^u, R¹, n, Y¹, R^2a, R^2b, R^2c, R^2d, R^2e, G¹, p1, p2, q1, q2, r, R³, R^3a, R^3b, R^3c, R^3d, R^3f, R^3g, R^3h, R³ⁱ, R^3j, R^3k, R^3l, R^3m, R³ⁿ, R^3p, R^3qR^3r, R^3s, R⁴, R⁵, and R⁶ is provided herein can be combined with every other variation or embodiment of R^a, R^b, R^q, R^s, R^t, R^u, R¹, n, Y¹, R^2a, R^2b, R^2c, R^2d, R^2e, G¹, p1, p2, q1, q2, r, R³, R^3a, R^3b, R^3c, R^3d, R^3f, R^3g, R^3h, R³ⁱ, R^3j, R^3k, R^3l, R^3m, R³ⁿ, R^3p, R^3q, R^3r, R^3s, R⁴, R⁵, and R⁶, the same as if each combination had been individually and specifically described.

Other embodiments will be apparent to those skilled in the art from the following detailed description.

As used herein, when any variable occurs more than one time in a chemical formula, its definition on each occurrence is independent of its definition at every other occurrence.

Formula (II) and/or Formula (I) include all subformulae thereof.

The compound names provided herein, including in Table 1, are provided by ChemBioDraw Professional 15.0. One of skilled in the art would understand that the compounds may be named or identified using various commonly recognized nomenclature systems and symbols. By way of example, the compounds may be named or identified with common names, systematic or non-systematic names. The nomenclature systems and symbols that are commonly recognized in the art of chemistry include, for example, Chemical Abstract Service (CAS), ChemBioDraw Ultra, and International Union of Pure and Applied Chemistry (IUPAC).

Compositions

Also provided are compositions, such as pharmaceutical compositions, that include a compound disclosed and/or described herein and one or more additional medicinal agents, pharmaceutical agents, adjuvants, carriers, excipients, and the like. Suitable medicinal and pharmaceutical agents include those described herein. In some embodiments, the pharmaceutical composition includes a pharmaceutically acceptable excipient or adjuvant and at least one chemical entity as described herein. Examples of pharmaceutically acceptable excipients include, but are not limited to, mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, sodium crosscarmellose, glucose, gelatin, sucrose, and magnesium carbonate. In some embodiments, provided are compositions, such as pharmaceutical compositions that contain one or more compounds described herein, or a pharmaceutically acceptable salt thereof.

In some embodiments, provided is a pharmaceutically acceptable composition comprising a compound of Formula (II) or Formula (I), such as a compound of Formula (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof. In some aspects, a composition may contain a synthetic intermediate that may be used in the preparation of a compound described herein. The compositions described herein may contain any other suitable active or inactive agents.

Any of the compositions described herein may be sterile or contain components that are sterile. Sterilization can be achieved by methods known in the art. Any of the compositions described herein may contain one or more compounds or conjugates that are substantially pure.

Also provided are packaged pharmaceutical compositions, comprising a pharmaceutical composition as described herein and instructions for using the composition to treat a patient suffering from a disease or condition described herein.

Methods of Use

Compounds and compositions detailed herein, such as a pharmaceutical composition comprising a compound of any formula provided herein, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient, may be used in methods of administration and treatment as provided herein.

Without being bound by theory, the compounds and pharmaceutical compositions disclosed herein are believed to act by modulating nicotinamide phosphoribosyltransferase (NAMPT). In some embodiments, the compounds and pharmaceutical compositions disclosed herein are activators of NAMPT. In some embodiments, provided are methods of treating a disease or condition mediated by NAMPT activity in an individual or subject, comprising administering to the individual or subject in need thereof a compound of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof. In some embodiments, provided are methods of treating cancer, a hyperproliferative disease or condition, an inflammatory disease or condition, a metabolic disorder, a cardiac disease or condition, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a neurological disease or injury, a neurodegenerative disorder or disease, diseases caused by impaired stem cell function, diseases caused by DNA damage, primary mitochondrial disorders, or a muscle disease or muscle wasting disorder in an individual or subject, comprising administering to the individual or subject in need thereof a compound of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof.

Also provided herein is the use of a compound of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for treatment of a disease or condition mediated by NAMPT activity in a subject. In some aspects, provided is a compound or composition as described herein for use in a method of treatment of the human or animal body by therapy. In some embodiments, provided herein are compounds of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof, for use in a method of treatment of the human or animal body by therapy. In some embodiments, provided herein are compounds of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof, for use in treating a disease or condition mediated by NAMPT activity. In some embodiments, the disease or condition is selected from the group consisting of cancer, a hyperproliferative disease or condition, an inflammatory disease or condition, a metabolic disorder, a cardiac disease or condition, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a neurological disease or injury, a neurodegenerative disorder or disease, diseases caused by impaired stem cell function, diseases caused by DNA damage, primary mitochondrial disorders, or a muscle disease or muscle wasting disorder.

Also provided herein are compositions (including pharmaceutical compositions) as described herein for the use in treating, preventing, and/or delaying the onset and/or development of a disease described herein and other methods described herein. In certain embodiments, the composition comprises a pharmaceutical formulation which is present in a unit dosage form.

In some embodiments, the subject is a mammal. In some embodiments, the subject is a mouse, rat, dog, cat, rabbit, pig, sheep, horse, cow, or human. In some embodiments, the subject is a human.

There are numerous conditions in which small molecule-mediated stimulation of NAMPT activity that boosts NAD+ levels would potentially be clinically beneficial (Stremland et al., Biochem Soc Trans. 2019, 47(1):119-130; Ralto et al., Nat Rev Nephrol. 2019; Fang et al., Trends Mol Med. 2017, 23(10):899-916; Yoshino et al., Cell Metab. 2011, 14(4):528-36; Yang and Sauve, Biochim Biophys Acta. 2016, 1864:1787-1800; Verdin, Science. 2015, 350(6265):1208-13). These conditions include, but are not limited to, cardiac diseases, chemotherapy induced tissue damage, renal diseases, metabolic diseases, muscular diseases, neurological diseases and injuries, diseases caused by impaired stem cell function, and DNA damage and primary mitochondrial disorders. In some embodiments, the disease or condition mediated by NAMPT activity is a cardiac disease, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a muscular disease, a neurological disease or injury, a disease caused by impaired stem cell function, or DNA damage and primary mitochondrial disorder.

Cardiac diseases. In various preclinical models of heart failure NAD as well as NAMPT levels are decreased. In these models, cardiac function can be rescued, either by restoring NAD via oral supplementation or overexpression of NAMPT (Diguet et al, Circulation. 2018, 137:2256-2273; Zheng et al., Clin Sci (Lond). 2019, 133(13):1505-1521; Smyrnias et al., J Am Coll Cardiol. 2019, 73(14):1795-1806). Thus, increasing the catalytic efficiency of NAMPT with a small molecule activator to compensate for the decreased protein levels is a promising strategy to treat various forms of heart failure.

Chemotherapy induced tissue damage. Use of chemotherapy regimens frequently is limited by toxicity to healthy tissues and severe oxidative stress is thought to play a major role. NAD boosting has been shown to trigger a strong anti-oxidant response. Therefore, NAMPT activators are considered broadly useful in various settings of chemotherapy to prevent reversible and irreversible secondary pathologies. Examples are anthracycline and trastuzumab cardiotoxicity, cisplatin induced kidney injury, peripheral neuropathies induced by cisplatin, paclitaxel, vincristine and other agents. Neuroprotection by NAMPT activation is also useful in treating/preventing chemotherapy associated cognitive (“chemo brain”), which is caused by destruction of healthy nerve tissue, both during active treatment and long after treatment has been halted. For instance, see Zheng et al., Clin Sci (Lond). 2019, 133(13):1505-1521.

Renal diseases. Renal diseases are highly prevalent and an area of urgent unmet medical need. In approximately 3% of hospitalized patients, acute kidney injury (AKI) is diagnosed. A subset of patients will progress to chronic kidney disease that may require long-term dialysis or kidney transplantation. A key feature of kidney dysfunction is a decrease in the activities of SIRT1 and SIRT3, characterized by a reduction of the sirtuin substrate NAD, primarily due to impairment of de novo NAD+ synthesis. NAMPT is robustly expressed during kidney injury, thus small molecule activation with NAMPT is considered an effective measure to prevent AKI. Similarly, kidney mesangial cell hypertrophy exhibits depletion of NAD+, and restoration of intracellular NAD+ levels is considered efficacious. For instance, see Poyan Mehr et al., Nat Med. 2018, September; 24(9): 1351-9.

Metabolic disease. NAD+ boosting improves insulin sensitivity, dyslipidemia, mitochondrial function in metabolic disease and protects from/improves non-alcoholic and alcoholic steatohepatitis in preclinical models. More than 3 million people per year in the U.S. alone are diagnosed with non-alcoholic steatohepatitis and it is one of the leading causes of liver transplantation. See Guarino and Dufour, Metabolites. 2019, Sep. 10; 9(9), pii: E180; Yoshino et al., Cell Metab. 2011, 14(4):528-36.

Muscular diseases. Preclinical data has suggested that NAD+ boosting strategies could alleviate skeletal muscle dysfunction in a number of conditions, including Duchenne's muscular dystrophy, and age-related sarcopenia. See Zhang et al., Clin Sci (Lond). 2019, 133(13):1505-1521; Mohamed et al., Aging (Albany NY). 2014, 6(10):820-34; Ryu et al., Sci Transl Med. 2016, 8(361):361ral39.

Neurological diseases and injuries. Repletion of NAD by means of NAMPT activation is neuroprotective and of therapeutic benefit in a wide range of preclinical models of neurological diseases and injuries, including age-related cognitive decline, glaucoma, ischemic stroke, and ALS. See Johnson et al., NPJ Aging Mech Dis. 2018, 4:10; Harlan et al., J Biol Chem. 2016, 291(20):10836-46; Zhao et al., Stroke. 2015, July; 46(7):1966-74; Williams et al., Front Neurosci. 2017, Apr. 25; 11:232.

Diseases caused by impaired stem cell function. NAD boosting promotes stem cell activation and hematopoiesis and is useful in accelerating the expansion of stem cell populations following a stem cell transplant. See Pi et al., Aging (Albany NY). 2019, 11(11):3505-3522.

DNA damage disorders and primary mitochondrial disorders. NAMPT activators will also be useful in the treatment of DNA damage disorders which are associated with an accelerated aging phenotype, such as Xeroderma pigmentosum, Cockayne syndrome, and Ataxia telangiectasia. Similarly, there are several primary mitochondrial disorders with shared symptoms and manifestations for which NAD boosting via NAMPT activation may be a suitable therapeutic intervention. See Fang et al, Cell. 2014, 157(4):882-896; Khan et al, EMBO Mol Med. 2014, June; 6(6):721-31; Cerutti et al., Cell Metab. 2014, 19(6):1042-9.

Provided in some embodiments are methods of treating a disease or condition mediated by NAMPT activity in a subject in need thereof, comprising administering to the individual or subject in need thereof a compound of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof, wherein the disease or condition is selected from the group consisting of cardiac diseases, chemotherapy induced tissue damage, renal diseases, metabolic diseases, muscular diseases, neurological diseases and injuries, diseases caused by impaired stem cell function, and DNA damage and primary mitochondrial disorders.

Additional applications of small molecule NAMPT activators are provided in Table 2.

TABLE 2
Cancer and     Anthracycline and trastuzumab cardiotoxicity
Chemotherapy   Proteasome inhibitor cardiotoxicity
induced tissue Cisplatin induced kidney injury
damage         Prevention/treatment of cognitive dysfunction resulting
               from chemotherapy (“chemo brain”)
               Chemotherapy induced impairment of hematopoiesis
               and myelosuppression
               Cachexia of cancer
               Chemoprevention of non-melanoma skin cancer in high
               risk patients
               chemoprevention of hepatocellular carcinoma
Cardiovascular Heart failure with reduced ejection fraction
diseases       Heart failure with preserved ejection fraction
               Hypertrophic cardiomyopathy
               Cardiac arrhythmias
               Duchenne Muscular Dystrophy-related cardiac
               dysfunction
               Cardiac dysfunction associated with Scleroderma,
               Lupus, Mitochondrial Disorders, Kawasaki Disease
               Hypertension
               Myocardial Infarction
Renal diseases Acute kidney injury including nephropathy following
               major surgeries including cardiac and vascular surgeries
               Acute kidney injury following hypotension,
               hemorrhagic shock, or cardiac arrest
               Acute kidney injury following exposure to contrast
               imaging agents used for MRI, CT scans, or other
               imaging modalities, particularly in the context of
               diabetes
               Chronic kidney disease
               Glomerular nephritis
               Kidney mesangial cell hypertrophy
               Arterial venous fistula maturation
Chronic        Chronic obstructive pulmonary disease
inflammatory   Asthma
and fibrotic   Scleroderma
diseases       Dermatomyositis
               Lupus erythematosus
               Rheumatoid arthritis and spondyloarthropathy
               Juvenile idiopathic arthritis
               Crohn's disease
               Inflammatory Bowel Disease
               Eczema
               Psoriasis and psoriatic arthritis
               Idiopathic pulmonary fibrosis
Vascular       Arterial and venous thrombosis
diseases       Ischemic Stroke
               Arteriosclerosis
Metabolic      Obesity
dysfunction    Diabetes
               Metabolic Syndrome
               Alcoholic steatohepatitis
               Non-alcoholic steatohepatitis
               Dyslipidemia
               Diabetic neuropathy
               Diabetic gastroparesis
Muscular       Muscular dystrophies, including: Duchenne, Becker's,
diseases       Congenital, Distal, Emery-Dreifuss', Facio-scapulo-
               humeral, Limb-girdle, myotonic, and oculopharyngeal
               Sarcopenia
               Frailty
               Polymyositis
               Muscle stem cell senescence developed in the context
               of nutritional deficiencies
               Non-mitochondrial myopathies such as inherited
               myopathies, myotonia, congenital myopathies selected
               from nemaline myopathy, multi/minicore myopathy,
               centronuclear myopathy and metabolic myopathies,
               inflammatory myopathies
Neurological   Depression
diseases       Frontotemporal dementia
and injuries   Multiple sclerosis
               Amyotrophic lateral sclerosis
               Peripheral neuropathy due to diabetes, chemotherapy
               Alzheimer's disease
               Parkinson's disease
               Huntington's Disease
               Spinal muscular atrophy
               Spinocerebellar ataxias
               Spastic paraplegias
               Glaucoma
               Age-related macular degeneration
               Age-related cognitive decline
               Noise induced and age-related hearing loss
               Ischemic stroke
               Traumatic brain injury
               Neonatal nerve damage
               Optic nerve injury
               Spinal cord injuries
               Peripheral neuropathies or tissue inflammation induced
               by cisplatin, paclitaxel, vincristine, other
               chemotherapeutic agents, or radiation.
               Peripheral neuropathies (length and non-length
               dependent) affecting motor, sensory, or autonomic
               nerves, arising from: diabetes, impaired glucose
               tolerance, hypertension, infection, trauma, autoimmune
               disorders, vasculitis, arteriosclerosis, vitamin
               deficiencies (particularly B6 and B12), alcoholism, liver
               or kidney disease, or exposure to toxins
DNA damage     Xeroderma pigmentosum
disorders and  Cockayne syndrome
Primary        Ataxia telangiectasia
Mitochondrial  MEGDEL syndrome
Disorders      Charcot-Marie-Tooth type 2
               Primary Mitochondrial Diseases (Disorders) including
               NARP, MELAS, Chronic Progressive External
               Ophthalmoplegia, Leigh's disease, Leber's Hereditary
               Optic Neuropathy, MERRF, Barth Syndrome, Luft
               Disease, Kearns Sayre Syndrome, Autosomal dominant
               optic atrophy
               Friedreich's ataxia
               Werner syndrome
General        Tissue repair following physical trauma, hemorrhagic
               shock, tissue grafting, organ transplant including heart,
               lung, liver, and kidney
               Stem cell therapies, including hematopoietic stem cell
               transfer, allogenic mesenchymal stem therapy for acute
               graft-vs-host disease, limbal stem cell deficiency due to
               genetic or acquired conditions that compromise normal
               turnover of the corneal epithelium

In some embodiments, the disease or condition mediated by NAMPT activity is cancer and chemotherapy-induced tissue damage, a cardiovascular disease, a renal disease, chronic inflammatory and fibrotic disease, a vascular disease, metabolic dysfunction, a muscular disease, a neurological disease or injury, or a DNA damage disorder or primary mitochondrial disorder. Provided in some embodiments are methods of treating a disease or condition mediated by NAMPT activity in a subject in need thereof, comprising administering to the individual or subject in need thereof a compound of Formula (II), (I), (I-A), (I-A1), (I-A2), (I-B), (I-C), (I-D), (I-E), (I-F), (I-G), (I-H), (I-J), or (I-K), or a compound of Table 1, or a pharmaceutically acceptable salt thereof. In some embodiments, the disease or condition is cancer or chemotherapy induced tissue damage, a cardiovascular disease, a renal disease, a chronic inflammatory or fibrotic disease, a vascular disease, metabolic dysfunction, a muscular disease, a neurological disease or injury, a DNA damage disorder or Primary Mitochondrial Disorder, including any of the diseases listed in Table 2.

Dosages

The compounds and compositions disclosed and/or described herein are administered at a therapeutically effective dosage, e.g., a dosage sufficient to provide treatment for the disease state. While human dosage levels have yet to be optimized for the chemical entities described herein, generally, a daily dose ranges from about 0.01 to 100 mg/kg of body weight; in some embodiments, from about 0.05 to 10.0 mg/kg of body weight, and in some embodiments, from about 0.10 to 1.4 mg/kg of body weight. Thus, for administration to a 70 kg person, in some embodiments, the dosage range would be about from 0.7 to 7000 mg per day; in some embodiments, about from 3.5 to 700.0 mg per day, and in some embodiments, about from 7 to 100.0 mg per day. The amount of the chemical entity administered will be dependent, for example, on the subject and disease state being treated, the severity of the affliction, the manner and schedule of administration and the judgment of the prescribing physician. For example, an exemplary dosage range for oral administration is from about 5 mg to about 500 mg per day, and an exemplary intravenous administration dosage is from about 5 mg to about 500 mg per day, each depending upon the compound pharmacokinetics.

A daily dose is the total amount administered in a day. A daily dose may be, but is not limited to be, administered each day, every other day, each week, every 2 weeks, every month, or at a varied interval. In some embodiments, the daily dose is administered for a period ranging from a single day to the life of the subject. In some embodiments, the daily dose is administered once a day. In some embodiments, the daily dose is administered in multiple divided doses, such as in 2, 3, or 4 divided doses. In some embodiments, the daily dose is administered in 2 divided doses.

Administration of the compounds and compositions disclosed and/or described herein can be via any accepted mode of administration for therapeutic agents including, but not limited to, oral, sublingual, subcutaneous, parenteral, intravenous, intranasal, topical, transdermal, intraperitoneal, intramuscular, intrapulmonary, vaginal, rectal, or intraocular administration. In some embodiments, the compound or composition is administered orally or intravenously. In some embodiments, the compound or composition disclosed and/or described herein is administered orally.

Pharmaceutically acceptable compositions include solid, semi-solid, liquid and aerosol dosage forms, such as tablet, capsule, powder, liquid, suspension, suppository, and aerosol forms. The compounds disclosed and/or described herein can also be administered in sustained or controlled release dosage forms (e.g., controlled/sustained release pill, depot injection, osmotic pump, or transdermal (including electrotransport) patch forms) for prolonged timed, and/or pulsed administration at a predetermined rate. In some embodiments, the compositions are provided in unit dosage forms suitable for single administration of a precise dose.

The compounds disclosed and/or described herein can be administered either alone or in combination with one or more conventional pharmaceutical carriers or excipients (e.g., mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, sodium crosscarmellose, glucose, gelatin, sucrose, magnesium carbonate). If desired, the pharmaceutical composition can also contain minor amounts of nontoxic auxiliary substances such as wetting agents, emulsifying agents, solubilizing agents, pH buffering agents and the like (e.g., sodium acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine acetate, triethanolamine oleate). Generally, depending on the intended mode of administration, the pharmaceutical composition will contain about 0.005% to 95%, or about 0.5% to 50%, by weight of a compound disclosed and/or described herein. Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pennsylvania.

In some embodiments, the compositions will take the form of a pill or tablet and thus the composition may contain, along with a compounds disclosed and/or described herein, one or more of a diluent (e.g., lactose, sucrose, dicalcium phosphate), a lubricant (e.g., magnesium stearate), and/or a binder (e.g., starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives). Other solid dosage forms include a powder, marume, solution or suspension (e.g., in propylene carbonate, vegetable oils or triglycerides) encapsulated in a gelatin capsule.

Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing or suspending etc. a compound disclosed and/or described herein and optional pharmaceutical additives in a carrier (e.g., water, saline, aqueous dextrose, glycerol, glycols, ethanol or the like) to form a solution or suspension. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, as emulsions, or in solid forms suitable for dissolution or suspension in liquid prior to injection. The percentage of the compound contained in such parenteral compositions depends, for example, on the physical nature of the compound, the activity of the compound and the needs of the subject. However, percentages of active ingredient of 0.01% to 10% in solution are employable, and may be higher if the composition is a solid which will be subsequently diluted to another concentration. In some embodiments, the composition will comprise from about 0.2 to 2% of a compound disclosed and/or described herein in solution.

Pharmaceutical compositions of the compounds disclosed and/or described herein may also be administered to the respiratory tract as an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the pharmaceutical composition may have diameters of less than 50 microns, or in some embodiments, less than 10 microns.

In addition, pharmaceutical compositions can include a compound disclosed and/or described herein and one or more additional medicinal agents, pharmaceutical agents, adjuvants, and the like. Suitable medicinal and pharmaceutical agents include those described herein.

Kits

Also provided are articles of manufacture and kits containing any of the compounds or pharmaceutical compositions provided herein. The article of manufacture may comprise a container with a label. Suitable containers include, for example, bottles, vials, and test tubes. The containers may be formed from a variety of materials such as glass or plastic. The container may hold a pharmaceutical composition provided herein. The label on the container may indicate that the pharmaceutical composition is used for preventing, treating or suppressing a condition described herein, and may also indicate directions for either in vivo or in vitro use.

In one aspect, provided herein are kits containing a compound or composition described herein and instructions for use. The kits may contain instructions for use in the treatment of a heart disease in an individual or subject in need thereof. A kit may additionally contain any materials or equipment that may be used in the administration of the compound or composition, such as vials, syringes, or IV bags. A kit may also contain sterile packaging.

Combinations

The compounds and compositions described and/or disclosed herein may be administered alone or in combination with other therapies and/or therapeutic agents useful in the treatment of the aforementioned disorders, diseases, or conditions.

ENUMERATED EMBODIMENTS

The following enumerated embodiments are representative of some aspects of the invention.

• • 1. A compound of Formula (I):

• • or a pharmaceutically acceptable salt thereof,
  • wherein:
  • Y¹ is

• •  and R¹ is selected from the group consisting of

• • or
  • Y¹ is

• •  R¹ is selected from the group consisting of

• • wherein
    • R^2a and R^2b are each independently halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, or —N(R^2e)C(O)(C₁-C₆ alkyl); and
    • R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl;
    • G¹ is CH or N;
    • p1 and p2 are each independently 0, 1, or 2;
    • q1 and q2 are each independently 1 or 2;
    • r is 1, 2, or 3;
  • n is 0 to 6;
    • wherein when Y¹ is

• • •  n is 4, 5, or 6; and
    • when Y¹ is

• • •  and r is 1, n is 2, 3, 4, 5, or 6;
  • R³ is selected from the group consisting of:
    • i. C₁-C₆ alkyl;
    • ii. C₆-C₁₄ aryl;
    • iii. optionally substituted 5- to 18-membered heteroaryl;
    • iv. —NR^3aR^3b, wherein
      • R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl);
    • v. —OR^3c, wherein
      • R³, is C₆-C₁₄ aryl;
    • vi. —C(O)R^3d, wherein
      • R^3d is selected from the group consisting of —NR 3R^3g; C₃-C₈ cycloalkyl; C₃-C₈ cycloalkyl substituted with optionally substituted C₆-C₁₄ aryl; C₃-C₈ cycloalkenyl; optionally substituted C₆-C₁₄ aryl; optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl); optionally substituted 3- to 18-membered heterocycloalkyl; and optionally substituted 5- to 18-membered heteroaryl,
      • wherein
        • R^3f and R^3g are each independently selected from the group consisting of:
        • (a) hydrogen,
        • (b) optionally substituted C₁-C₆ alkyl,
        • (c) C₆-C₁₄ aryl,
        • (d) optionally substituted 3- to 18-membered heterocycloalkyl,
        • (e) optionally substituted 5- to 18-membered heteroaryl,
        • (f) optionally substituted C₃-C₁₀ cycloalkyl; and
        • (g) optionally substituted C₃-C₁₀ cycloalkenyl;
    • vii. C₁-C₆ alkyl substituted with C(O)NR^3hR³ⁱ, optionally substituted 3- to 18-membered heterocycloalkyl, or optionally substituted 5- to 18-membered heteroaryl,
      • wherein R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
    • viii. —C(O)OR^3j, wherein
      • R^3j is hydrogen or C₁-C₆ alkyl;
    • ix. —NHC(O)R^3k, wherein
      • R^3k is optionally substituted C₆-C₁₄ aryl, optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), or optionally substituted 5- to 18-membered heteroaryl;
    • x. —NHC(O)OR³¹, wherein
      • R^3l is hydrogen or C₁-C₆ alkyl;
    • xi. —NHSO₂R^3m, wherein
      • R^3m is optionally substituted 5- to 18-membered heteroaryl, optionally substituted C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), each of which is optionally substituted; and
    • xii. —SO₂R³ⁿ; wherein
      • R³ⁿ is optionally substituted C₃-C₁₀ cycloalkyl, optionally substituted C₆-C₁₄ aryl, or optionally substituted —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl);
  • R⁴ is phenyl or —C(O)NH—CH₂-phenyl;
  • R^5a and R^5b are independently selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl); and
  • R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), and —C(O)-phenyl; and
  • wherein
    • (1) when Y¹ is

• • •  and n is 0 or 1, R¹ is selected from the group consisting of

• • •  and
    • (2) when Y¹ is

• • •  and n is 0, R¹ is selected from the group consisting of

• • 2. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 3. The compound of embodiment 1 or embodiment 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 1 and q1 is 1.
  • 4. The compound of embodiment 1 or embodiment 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 2 and q1 is 1.
  • 5. The compound of embodiment 1 or embodiment 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 2 and q1 is 2.
  • 6. The compound of any one of embodiments 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 1 and q2 is 1.
  • 7. The compound of any one of embodiments 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 0 and q2 is 1.
  • 8. The compound of any one of embodiments 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 1 and q2 is 2.
  • 9. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is C₁-C₆ alkyl.
  • 10. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is C₆-C₁₄ aryl.
  • 11. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is 5- to 18-membered heteroaryl optionally substituted with C₁-C₆ alkyl.
  • 12. The compound of embodiment 11, or a pharmaceutically acceptable salt thereof, wherein R³ is pyridyl or pyrimidyl optionally substituted with C₁-C₆ alkyl.
  • 13. The compound of embodiment 11 or embodiment 12, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 14. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —NR^3aR^3b, wherein R^3a and R^3b are each independently selected from the group consisting of hydrogen, C₆-C₁₄ aryl, 5- to 18-membered heteroaryl, —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), and —(C₁-C₆ alkylene)-(5- to 18-membered heteroaryl).
  • 15. The compound of embodiment 14, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 16. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is OR^3c, wherein R^3c is C₆-C₁₄ aryl.
  • 17. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —C(O)R^3d.
  • 18. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is —NR3^fR^3g and R^3f and R^3g are each independently selected from the group consisting of:
    • (a) hydrogen,
    • (b) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of —OH, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl, wherein the C₆-C₁₄ aryl and 5- to 18-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, hydroxyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, and CN,
    • (c) C₆-C₁₄ aryl,
    • (d) 3- to 18-membered heterocycloalkyl,
    • (e) 5- to 18-membered heteroaryl optionally substituted with methyl or CN,
    • (f) C₃-C₁₀ cycloalkyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl; and
    • (g) C₃-C₁₀ cycloalkenyl optionally substituted with one or more substituents selected from the group consisting of halo, hydroxyl, C₁-C₆ alkyl optionally substituted with hydroxyl, C₆-C₁₄ aryl, and 5- to 18-membered heteroaryl.
  • 19. The compound of embodiment 17 or embodiment 18, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 20. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is C₃-C₈ cycloalkyl.
  • 21. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is C₃-C₈ cycloalkyl substituted with C₆-C₁₄ aryl, wherein the C₆-C₁₄ aryl is optionally substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆ alkoxy.
  • 22. The compound of embodiment 20 or embodiment 21, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 23. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is C₃-C₈ cycloalkenyl.
  • 24. The compound of embodiment 23, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 24. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is C₆-C₁₄ aryl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, cyano, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆haloalkyl, —(C₁-C₆ alkylene)-OH, —C(O)O(C₁-C₆ alkyl), —NR^3e1R^3e2, —S(O)₂(C₁-C₆ alkyl), 5- to 18-membered heteroaryl, and 3- to 18-membered heterocycloalkyl optionally substituted with oxo, wherein R^3e1 and R^3e2 are each independently H or C₁-C₆ alkyl.
  • 25. The compound of embodiment 24, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 26. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) optionally substituted with one or more substituents selected from the group consisting of halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆alkoxy.
  • 27. The compound of embodiment 26, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 28. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is 3- to 18-membered heterocycloalkyl optionally substituted with one or more substituents selected from the group consisting of
    • (a) C₁-C₆ alkyl optionally substituted with one or more substituents selected from the group consisting of hydroxyl, halo, C₃-C₁₀ cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C₁-C₆ alkyl substituents,
    • (b) C₆-C₁₄ aryl,
    • (c) 3- to 18-membered heterocycloalkyl,
    • (d) —C(O)O(C₁-C₆ alkyl),
    • (e) —C(O)(C₆-C₁₄ aryl),
    • (f) halo, and
    • (g) C₁-C₆ alkoxy optionally substituted with one or more halo substituents.
  • 29. The compound of embodiment 28, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 30. The compound of embodiment 17, or a pharmaceutically acceptable salt thereof, wherein R^3d is 5- to 18-membered heteroaryl optionally substituted with one or more substituents selected from the group consisting of C₁-C₆ alkyl, hydroxyl, oxo, and 3- to 18-membered heterocycloalkyl.
  • 31. The compound of embodiment 30, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 32. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is C₁-C₆ alkyl substituted with C(O)NR^3hR³ⁱ, wherein R^3h and R³ⁱ are each independently selected from C₁-C₆ alkyl and —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl).
  • 33. The compound of embodiment 32, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 34. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is C₁-C₆ alkyl substituted with 3- to 18-membered heterocycloalkyl, wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more substituents selected from halo and C₆-C₁₄ aryl. 35. The compound of embodiment 34 or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 36. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is C₁-C₆ alkyl substituted with 5- to 18-membered heteroaryl.
  • 37. The compound of embodiment 36, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 38. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —C(O)OR^3j, wherein R^3j is hydrogen or C₁-C₆ alkyl.
  • 39. The compound of embodiment 38, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 40. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —NHC(O)R^3k.
  • 41. The compound of embodiment 40, or a pharmaceutically acceptable salt thereof, wherein R^3k is C₆-C₁₄ aryl optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl.
  • 42. The compound of embodiment 40 or 41, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 43. The compound of embodiment 40, or a pharmaceutically acceptable salt thereof, wherein R^3k is —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl.
  • 44. The compound of embodiment 40 or 43, or a pharmaceutically acceptable salt thereof, wherein R is

• • 45. The compound of embodiment 40, or a pharmaceutically acceptable salt thereof, wherein R^3k is 5- to 18-membered heteroaryl optionally substituted with one or more substituents independently selected from the group consisting of C₁-C₆ alkyl, cyano, —NR^3k1R^3k2, hydroxy, alkoxy, and S(O)₂(alkyl), wherein R^3k1 and R^3k2 are each independently hydrogen or C₁-C₆ alkyl.
  • 46. The compound of embodiment 40 or 45, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 47. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —NHC(O)OR^3l, wherein R^3l is hydrogen or C₁-C₆ alkyl.
  • 48. The compound of embodiment 47, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 49. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —NHSO₂R^3m, wherein R^3m is 5- to 18-membered heteroaryl, C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the 5- to 18-membered heteroaryl, the C₆-C₁₄ aryl, and the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) are each optionally substituted with one or more substituents selected from halo and C₁-C₆ alkoxy.
  • 50. The compound of embodiment 49, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 51. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein R³ is —SO₂R³ⁿ and R³ⁿ is C₃-C₁₀ cycloalkyl, C₆-C₁₄ aryl, or —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl), wherein the C₃-C₁₀ cycloalkyl, the C₆-C₁₄ aryl, and the —(C₁-C₆ alkylene)-(C₆-C₁₄ aryl) are each optionally substituted with one or more substituents selected from halo and —C(O)O(C₁-C₆ alkyl).
  • 52. The compound of embodiment 51, or a pharmaceutically acceptable salt thereof, wherein R³ is

• • 53. The compound of any one of embodiments 1-52, or a pharmaceutically acceptable salt thereof, wherein G¹ is CH.
  • 54. The compound of any one of embodiments 1-52, or a pharmaceutically acceptable salt thereof, wherein G¹ is N.
  • 55. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 56. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 57. The compound of embodiment 56, or a pharmaceutically acceptable salt thereof, wherein r is 1.
  • 58. The compound of embodiment 56, or a pharmaceutically acceptable salt thereof, wherein r is 2.
  • 59. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 60. The compound of embodiment 59, or a pharmaceutically acceptable salt thereof, wherein R⁴ is phenyl.
  • 61. The compound of embodiment 59, or a pharmaceutically acceptable salt thereof, wherein R⁴ is —C(O)NH—CH₂-phenyl.
  • 62. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 63. The compound of embodiment 62, or a pharmaceutically acceptable salt thereof, wherein R^5a is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl).
  • 64. The compound of embodiment 62 or embodiment 63, or a pharmaceutically acceptable salt thereof, wherein R^5b is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C₁-C₆ alkyl).
  • 65. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein Y¹ is

• • 66. The compound of embodiment 65, or a pharmaceutically acceptable salt thereof, wherein R⁶ is selected from the group consisting of —C(O)OC(CH₃)₃, —NHC(O)O(C₁-C₆ alkyl), and —C(O)-phenyl.
  • 67. The compound of any one of embodiments 1-54, 56, and 58-66, or a pharmaceutically acceptable salt thereof, n is 0.
  • 68. The compound of any one of embodiments 1-54, 56, and 58-66, or a pharmaceutically acceptable salt thereof, wherein n is 1.
  • 69. The compound of any one of embodiments 1-54 and 58-66, or a pharmaceutically acceptable salt thereof, wherein n is 2.
  • 70. The compound of any one of embodiments 1-54 and 56-66, or a pharmaceutically acceptable salt thereof, wherein n is 3.
  • 71. The compound of any one of embodiments 1-66, or a pharmaceutically acceptable salt thereof, wherein n is 4.
  • 72. The compound of any one of embodiments 1-66, or a pharmaceutically acceptable salt thereof, wherein n is 5.
  • 73. The compound of any one of embodiments 1-66, or a pharmaceutically acceptable salt thereof, wherein n is 6.
  • 74. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• • 75. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• • 76. The compound of any one of embodiments 1-58 and 67-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• •  and R^2a is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl), wherein R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl.
  • 77. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is selected from the group consisting of

• • 78. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• •  and R^2b is selected from the group consisting of halo, —O(C₁-C₆ alkyl), C₁-C₆ alkyl substituted with —OH, —C(O)NR^2cR^2d, and —N(R^2e)C(O)(C₁-C₆ alkyl), wherein R^2c, R^2d, and R^2e are each independently hydrogen or C₁-C₆ alkyl.
  • 79. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• • 80. The compound of any one of embodiments 1-73, or a pharmaceutically acceptable salt thereof, wherein R¹ is

• • 81. A compound selected from the group consisting of compounds of Table 1, or a pharmaceutically acceptable salt thereof.
  • 82. A pharmaceutical composition comprising a compound according to any one of embodiments 1-81, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.
  • 83. A method of treating a disease or condition mediated by NAMPT activity in a subject in need thereof, comprising administering to the subject a compound of any one of embodiments 1-81, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 82.
  • 84. The method of embodiment 83, wherein the disease or condition is selected from the group consisting of cancer, a hyperproliferative disease or condition, an inflammatory disease or condition, a metabolic disorder, a cardiac disease or condition, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a neurological disease or injury, a neurodegenerative disorder or disease, diseases caused by impaired stem cell function, diseases caused by DNA damage, primary mitochondrial disorders, or a muscle disease or muscle wasting disorder.
  • 85. The method of embodiment 83, wherein the disease or condition is selected from the group consisting of obesity, atherosclerosis, insulin resistance, type 2 diabetes, cardiovascular disease, Alzheimer's disease, Huntington's disease, Parkinson's disease, amyotrophic lateral sclerosis, depression, Down syndrome, neonatal nerve injury, aging, axonal degeneration, carpal tunnel syndrome, Guillain-Barre syndrome, nerve damage, polio (poliomyelitis), and spinal cord injury.

General Synthetic Methods

Compounds of Formula (II) or Formula (I), or any variation or embodiment thereof, or a salt of any of the foregoing, will now be described by reference to illustrative synthetic schemes for their general preparation below and the specific examples that follow. Artisans will recognize that, to obtain the various compounds herein, starting materials may be suitably selected so that the ultimately desired substituents will be carried through the reaction scheme with or without protection as appropriate to yield the desired product. Alternatively, it may be necessary or desirable to employ, in the place of the ultimately desired substituent, a suitable group that may be carried through the reaction scheme and replaced as appropriate with the desired substituent. In addition, one of skill in the art will recognize that protecting groups may be used to protect certain functional groups (amino, carboxy, or side chain groups) from reaction conditions, and that such groups are removed under standard conditions when appropriate. Unless otherwise specified, the variables are as defined above in reference to Formula (II) or Formula (I).

Where it is desired to obtain a particular enantiomer of a compound, this may be accomplished from a corresponding mixture of enantiomers using any suitable conventional procedure for separating or resolving enantiomers. Thus, for example, diastereomeric derivatives may be produced by reaction of a mixture of enantiomers, e.g. a racemate, and an appropriate chiral compound. The diastereomers may then be separated by any convenient means, for example by crystallization and the desired enantiomer recovered. In another resolution process, a racemate may be separated using chiral High Performance Liquid Chromatography. Alternatively, if desired a particular enantiomer may be obtained by using an appropriate chiral intermediate in one of the processes described.

Chromatography, recrystallization and other conventional separation procedures may also be used with intermediates or final products where it is desired to obtain a particular isomer of a compound or to otherwise purify a product of a reaction.

Particular non-limiting examples are provided in the Example section below.

EXAMPLES

The following examples are offered to illustrate but not to limit the compositions, uses, and methods provided herein. The compounds are prepared using the general methods described above.

The following abbreviations are used throughout the Examples: TEA (triethylamine), DCM (dichloromethane), (Boc)₂O (di-tert-butyl dicarbonate), EA (Ethyl acetate), PE (Petroleum ether), DMF (N,N-dimethylformamide), DIEA (N-ethyl-N-isopropylpropan-2-amine), HATU (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate), HOAt (1-Hydroxy-7-azabenzotriazole), HOBt (Hydroxybenzotriazole), EDCI (1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide), MeOH (methanol), EtOH (ethanol), iPrOH (propan-2-ol), ACN (acetonitrile), TFA (trifluoroacetic acid), DPPA (Diphenylphosphoryl azide), DBU (1,8-Diazabicyclo(5.4.0)undec-7-ene), THF (tetrahydrofuran), PPh₃ (triphenylphosphane), SM (starting material), Hex (hexane), NCS (N-chlorosuccinimide), r.t. (room temperature), DCE (dichloroethane), FA (formic acid), CHCl₃ (Chloroform), BnBr (benzyl bromide), HCl (hydrogen chloride), equiv (equivalent), and DSC (bis(2,5-dioxopyrrolidin-1-yl) carbonate), HBTU (O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate).

Example A

Synthesis of Compound 168, Compound 201, and Intermediate 1.15

Preparation of methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylate (Compound 168). 1-Chloro-4-(isocyanatomethyl)benzene (6.8 g, 40.8 mmol, 1 equiv) was added to a stirring solution of methyl 6-aminospiro[3.3]heptane-2-carboxylate (8.4 g, 40.8 mmol, 1 equiv) in CH₂Cl₂ (100 mL) at rt. After 12 h, the solvent was removed by rotary evaporation, the crude material triturated in EtOH (100 mL) for 10 min, filtered, washed with EtOH (2×25 mL), and dried under high vacuum to give the Compound 168 (12 g, 87%) as a white solid. LRMS (APCI) m/z 337.1 (M+H). ¹H NMR (400 MHz, Methanol-d4) δ 7.31 (d, J=8.6 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J=8.0 Hz, 1H), 3.66 (s, 3H), 3.37 (s, 3H), 3.06 (p, J=8.6 Hz, 1H), 2.49 (ddd, J=11.8, 7.4, 5.2 Hz, 1H), 2.33 (tq, J=8.5, 3.2, 2.5 Hz, 3H), 2.28-2.07 (m, 2H), 1.87 (ddd, J=25.8, 11.2, 8.6 Hz, 2H).

Chiral Separation of methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid. Five grams of methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylate were resolved by chiral SFC (Chiralpak AD-H, 30% co-solvent (EtOH w/0.25% isopropylamine) at 70 g/min) affording the two chiral fragments Compound 201 (2.4 g, 48%) and Intermediate 1.15 (2.4 g, 48%) as white solids. The absolute stereochemistry of each fragment was not confirmed. Compound 201 elutes first from SFC using stated conditions, followed by Intermediate 1.15.

Compound 201: LRMS (APCI) m/z 337.1 (M+H). ¹H NMR (400 MHz, Methanol-d4) δ 7.32 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J=8.0 Hz, 1H), 3.66 (s, 3H), 3.06 (p, J=8.5 Hz, 1H), 2.49 (ddd, J=11.7, 7.3, 5.5 Hz, 1H), 2.39-2.28 (m, 3H), 2.28-2.10 (m, 2H), 1.87 (ddd, J=25.9, 11.1, 8.7 Hz, 2H).

Intermediate 1.15: LRMS (APCI) m/z 337.1 (M+H). ¹H NMR (400 MHz, Methanol-d4) δ 7.32 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J=8.0 Hz, 1H), 3.66 (s, 3H), 3.06 (p, J=8.5 Hz, 1H), 2.49 (ddd, J=11.6, 7.2, 5.3 Hz, 1H), 2.39-2.28 (m, 3H), 2.28-2.11 (m, 2H), 1.87 (ddd, J=25.8, 11.0, 8.7 Hz, 2H).

Compounds 35, 8, 197, 37, 151, 152, 83, 81, 82, and 36 as well as Intermediates 1.3 and 1.7 were prepared in a similar manner as Compound 168, using the reagents provided in the table below in place of methyl 6-aminospiro[3.3]heptane-2-carboxylate and 1-chloro-4-(isocyanatomethyl)benzene.

Compound
No.	Amine	Isocyanate	Structure, Name and Data
Compound 35	methyl 6- aminospiro [3.3]heptane- 2- carboxylate	4-methoxy benzyl isocyanate
			Methyl 6-(3-(4-methoxybenzyl)ureido)
			spiro[3.3]heptane-2-carboxylate. LCMS-ESI
			(POS.) m/z: 333 (M + H)+. 1H NMR (400 MHz,
			DMSO-d6) δ 7.15 (d, J = 8.3 Hz, 2H), 6.91-
			6.78 (m, 2H), 6.16-6.03 (m, 2H), 4.09 (d, J =
			5.9 Hz, 2H), 3.91 (q, J = 8.1 Hz, 1H), 3.73 (d, J =
			1.8 Hz, 3H), 3.58 (d, J = 1.8 Hz, 3H), 3.03 (p,
			J = 8.4 Hz, 1H), 2.34 (s, 1H), 2.30-2.22 (m,
			1H), 2.14 (dt, J = 26.5, 8.6 Hz, 4H), 1.76 (dt, J =
			27.2, 9.8 Hz, 2H).
Intermediate 1.3	methyl 6- aminospiro [3.3]heptane- 2- carboxylate	4-fluoro benzyl isocyanate
			6-(3-(4-
			fluorobenzyl)ureido)spiro[3.3]heptane-2-
			carboxylic acid. LCMS-ESI (POS.) m/z: 321
Compound 197	tert-butyl 6-amino- 2- azaspiro[3.3] heptane- 2- carboxylate	4-chloro benzyl isocyanate
			tert-butyl 6-(3-(4-chlorobenzyl)ureido)-2-
			azaspiro[3.3]heptane-2-carboxylate. LRMS
			(APCI) m/z 280.1 (M + H− Boc). 1H NMR (400
			MHz, Methanol-d4) δ 7.32 (d, J = 8.5 Hz, 2H),
			7.26 (d, J = 8.4 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J =
			8.1 Hz, 1H), 3.98-3.91 (m, 2H), 3.84 (s, 2H),
			2.55 (ddd, J = 10.0, 7.6, 2.9 Hz, 2H), 2.06 (td, J =
			8.9, 2.9 Hz, 2H), 1.44 (s, 9H).
Compound 37	tert-butyl 6-amino- 2- azaspiro[3.3] heptane- 2- carboxylate	4-methoxy benzyl isocyanate
			tert-butyl 6-(3-(4-methoxybenzyl)ureido)-2-
			azaspiro[3.3]heptane-2-carboxylate. LRMS
			(APCI) m/z 276.1 (M + H − Boc). 1H NMR (400
			MHz, DMSO-d6) δ 7.21-7.09 (m, 2H), 6.93-
			6.75 (m, 2H), 6.24-6.04 (m, 2H), 4.10 (d, J =
			5.8 Hz, 2H), 3.93 (p, J = 8.1 Hz, 1H), 3.85 (s,
			2H), 3.77-3.64 (m, 5H), 2.41 (ddd, J = 11.7,
			6.5, 2.4 Hz, 2H), 2.06-1.86 (m, 2H), 1.37 (d, J =
			1.4 Hz, 9H).
Intermediate 1.7	tert-butyl 6-amino- 2- azaspiro[3.3] heptane- 2- carboxylate	4- (isocyanato- methyl)ben- zamide
			tert-butyl 6-(3-(4-carbamoylbenzyl)ureido)-2-
			azaspiro[3.3]heptane-2-carboxylate. LRMS
			(APCI) m/z 289 (M + H− Boc).
Compound 151	tert-butyl (2r,4s)-2- amino-6- azaspiro[3.4] octane- 6- carboxylate	4-chloro benzyl isocyanate
			tert-butyl (2r,4s)-2-(3-(4-
			chlorobenzyl)ureido)-6-azaspiro[3.4]octane-6-
			carboxylate. LRMS (APCI) m/z 394.2 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.40-7.32
			(m, 2H), 7.29-7.22 (m, 2H), 6.36-6.25 (m,
			2H), 4.17 (d, J = 4.9 Hz, 2H), 4.03 (d, J = 8.1
			Hz, 1H), 3.20 (d, J = 20.8 Hz, 4H), 2.19 (d, J =
			9.3 Hz, 2H), 1.84-1.70 (m, 4H), 1.40 (s, 9H).
Compound 152	tert-butyl (2s,4r)-2- amino-6- azaspiro[3.4] octane- 6- carboxylate	4-chloro benzyl isocyanate
			tert-butyl (2s,4r)-2-(3-(4-
			chlorobenzyl)ureido)-6-azaspiro[3.4]octane-6-
			carboxylate. LRMS (APCI) m/z 394.2 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.40-7.32
			(m, 2H), 7.29-7.22 (m, 2H), 6.36-6.25 (m,
			2H), 4.17 (d, J = 4.9 Hz, 2H), 4.03 (d, J = 8.1
			Hz, 1H), 3.20 (d, J = 20.8 Hz, 4H), 2.19 (d, J =
			9.3 Hz, 2H), 1.84-1.70 (m, 4H), 1.40 (s, 9H).
Compound 83	tert-butyl- 2-amino- 6-azaspiro[3.4] octane- 6- carboxylate	4-methoxy benzyl isocyanate
			tert-butyl 2-(3-(4-methoxybenzyl)ureido)-6-
			azaspiro[3.4]octane-6-carboxylate. LRMS
			(APCI) m/z 390.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.16 (d, J = 8.0 Hz, 2H), 6.95-
			6.78 (m, 2H), 6.08 (t, J = 6.0 Hz, 1H), 5.91 (d, J =
			7.3 Hz, 1H), 4.11 (d, J = 5.8 Hz, 2H), 3.87 (q,
			J = 7.0 Hz, 1H), 3.73 (s, 3H), 3.71-3.61 (m,
			4H), 2.05 (dd, J = 13.2, 7.4 Hz, 1H), 1.86 (dq, J =
			12.6, 6.3, 5.7 Hz, 2H), 1.73 (q, J = 8.0, 6.3 Hz,
			1H), 1.58 (dd, J = 13.2, 6.6 Hz, 1H), 1.37 (d, J =
			1.6 Hz, 9H), 1.35-1.29 (m, 1H).
Compound 81	tert-butyl (2r,4s)-2- amino-6- azaspiro[3.4] octane- 6- carboxylate	4-methoxy benzyl isocyanate
			tert-butyl (2r,4s)-2-(3-(4-
			methoxybenzyl)ureido)-6-azaspiro[3.4]octane-
			6-carboxylate. LRMS (APCI) m/z 390.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.15
			(d, J = 8.0 Hz, 2H), 6.91-6.83 (m, 2H), 6.23-
			6.14 (m, 2H), 4.11 (d, J = 5.8 Hz, 2H), 4.03 (q, J =
			8.2 Hz, 1H), 3.72 (s, 3H), 3.23 (d, J = 6.2 Hz,
			2H), 3.18 (d, J = 6.9 Hz, 2H), 2.20 (t, J = 9.3 Hz,
			2H), 1.78 (t, J = 9.5 Hz, 4H), 1.40 (s, 9H).
Compound 82	tert-butyl (2s,4r)-2- amino-6- azaspiro[3.4] octane- 6- carboxylate	4-methoxy benzyl isocyanate
			tert-butyl (2s,4r)-2-(3-(4-
			methoxybenzyl)ureido)-6-azaspiro[3.4]octane-
			6-carboxylate. LRMS (APCI) m/z 390.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.15
			(d, J = 8.0 Hz, 2H), 6.87 (d, J = 8.0 Hz, 2H),
			6.25-6.08 (m, 2H), 4.10 (d, J = 6.0 Hz, 2H),
			4.08-4.00 (m, 1H), 3.72 (s, 3H), 3.26-3.18
			(m, 2H), 3.13 (s, 2H), 2.22-2.09 (m, 2H), 1.81
			(t, J = 8.9 Hz, 4H), 1.39 (s, 9H).
Compound 36	tert-butyl (5- aminopentyl) carbamate	4-methoxy benzyl isocyanate
			tert-butyl (5-(3-(4-
			methoxybenzyl)ureido)pentyl)carbamate.
			LRMS (APCI) m/z 366 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.16 (d, J = 8.1 Hz, 2H),
			6.87 (dd, J = 8.3, 1.5 Hz, 2H), 6.80-6.73 (m,
			1H), 6.16 (t, J = 6.1 Hz, 1H), 5.85 (t, J = 5.8 Hz,
			1H), 4.12 (d, J = 5.8 Hz, 2H), 3.73 (s, 3H), 2.98
			(q, J = 6.6 Hz, 2H), 2.89 (q, J = 6.7 Hz, 2H),
			1.41-1.29 (m, 13H), 1.22 (q, J = 8.2 Hz, 2H).
Intermediate 1.16	methyl 5- aminopenta- noate	4-chloro benzyl isocyanate
			Methyl 5-(3-(4-
			chlorobenzyl)ureido)pentanoate.
			LRMS (APCI) m/z 299.1 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.36 (d, J = 8.3 Hz, 2H), 7.25
			(d, J = 8.3 Hz, 2H), 6.35 (t, J = 6.2 Hz, 1H), 5.99
			(t, J = 5.8 Hz, 1H), 4.17 (d, J = 6.1 Hz, 2H), 3.59
			(s, 3H), 3.00 (q, J = 6.5 Hz, 2H), 2.31 (t, J = 7.4
			Hz, 2H), 1.58-1.44 (m, 2H), 1.44-1.33 (m, 2H).
Intermediate 1.17	methyl 6- aminohex- anoate	4-chloro benzyl isocyanate
			Methyl 6-(3-(4-
			chlorobenzyl)ureido)hexanoate. LRMS
			(APCI) m/z 313.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.36 (d, J = 8.4 Hz, 2H), 7.26 (d, J =
			8.2 Hz, 2H), 6.45 (t, J = 6.1 Hz, 1H), 6.07 (t, J =
			5.8 Hz, 1H), 4.17 (d, J = 6.1 Hz, 2H), 3.58 (s,
			3H), 2.98 (q, J = 6.5 Hz, 2H), 2.29 (t, J = 7.4 Hz,
			2H), 1.52 (p, J = 7.4 Hz, 2H), 1.42-1.32 (m, 4H).
Intermediate 1.18	tert-butyl (5- aminopentyl) carbamate	4-chloro benzyl isocyanate
			tert-butyl (5-(3-(4-
			chlorobenzyl)ureido)pentyl)carbamate. LRMS
			(APCI) m/z 370.1 (M + H).
Intermediate 1.19	tert-butyl 4-(4- aminobutyl) piperidine- 1- carboxylate	4-chloro benzyl isocyanate
			tert-butyl 4-(4-(3-(4-
			chlorobenzyl)ureido)butyl)piperidine-1-
			carboxylate. LRMS (APCI) m/z 424.1 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.36 (d, J =
			8.1 Hz, 2H), 7.25 (d, J = 8.1 Hz, 2H), 6.31 (t, J =
			6.0 Hz, 1H), 5.92 (t, J = 5.7 Hz, 1H), 4.17 (d, J =
			6.1 Hz, 2H), 3.91 (d, J = 12.9 Hz, 2H), 2.99 (q, J =
			6.4 Hz, 2H), 2.67 (s, 2H), 1.64-1.55 (m, 2H),
			1.39 (s, 9H), 1.35 (t, J = 6.9 Hz, 3H), 1.22 (dd, J =
			16.4, 7.5 Hz, 4H), 0.93 (qd, J = 12.3, 4.2 Hz,
			2H).
Intermediate 1.20	tert-butyl 4-(4- aminobutyl) piperazine- 1- carboxylate	4-chloro benzyl isocyanate
			tert-butyl 4-(4-(3-(4-
			chlorobenzyl)ureido)butyl)piperazine-1-
			carboxylate. LRMS (APCI) m/z 425.2 (M + H ).
Intermediate 1.21	Intermediate 20.1	5-(isocyanato- methyl)oxa- zole
			tert-butyl 4-(4-(3-(oxazol-5-
			ylmethyl)ureido)butyl-4,4-d2)piperidine-1-
			carboxylate. LRMS (APCI) m/z 327 (M + H −
			tBu).

Example B

Synthesis of Intermediates 2.1, 2.4, and 2.5

Preparation of 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (Intermediate 2.1). LiOH (622 mg, 25.98 mmol, 1.25 equiv) and methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylate (Compound 168) (7 g, 20.78 mmol, 1 equiv) were suspended in MeOH/H2O (50 mL/5 mL) and heated to 60° C. After 1 h, the reaction was cooled to rt and solvent removed by rotary evaporation. The crude material was dissolved in H2O/MeOH (90 mL/10 mL) before being precipitated with 3M HCl, filtered, washed with water (3×20 mL), and dried under high vacuum to give the desired product 2.1 as a white solid (5.2 g, 78%). LRMS (APCI) m/z 323.0 (M+H). ¹H NMR (400 MHz, Methanol-d4) δ 7.31 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J=8.1 Hz, 1H), 3.02 (p, J=8.4 Hz, 1H), 2.56-2.43 (m, 1H), 2.33 (td, J=9.8, 8.4, 6.0 Hz, 3H), 2.29-2.11 (m, 2H), 1.87 (ddd, J=24.6, 11.0, 8.7 Hz, 2H).

Chiral Separation of 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid. Five grams of 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid was resolved by chiral SFC (Chiralpak AD-H, 30% co-solvent [EtOH w/0.25% isopropylamine] at 70 g/min) affording the two chiral fragments 2.4 (2.3 g, 46%) and 2.5 (2.1 g, 42%) as white solids. The absolute stereochemistry of each fragment was not confirmed. Intermediate 2.4 elutes first from SFC using stated conditions, followed by intermediate 2.5.

Intermediate 2.4: LRMS (APCI) m/z 323.1 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, J=8.4 Hz, 2H), 7.24 (d, J=8.4 Hz, 2H), 6.40 (t, J=6.1 Hz, 1H), 6.29 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.89 (h, J=8.1 Hz, 1H), 3.09 (p, J=6.4 Hz, 1H), 2.75 (p, J=8.5 Hz, 1H), 2.31 (ddd, J=10.7, 7.3, 5.2 Hz, 1H), 2.20-2.01 (m, 4H), 2.01-1.90 (m, 1H), 1.82-1.63 (m, 2H), 1.06 (d, J=6.3 Hz, 5H). (complexed isopropanol found)

Intermediate 2.5: LRMS (APCI) m/z 323.1 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, J=8.4 Hz, 2H), 7.24 (d, J=8.2 Hz, 2H), 6.36 (t, J=6.1 Hz, 1H), 6.25 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.89 (h, J=8.0 Hz, 1H), 3.07 (p, J=6.4 Hz, 1H), 2.78 (p, J=8.5 Hz, 1H), 2.36-2.25 (4, 1H), 2.11 (tdd, J=19.6, 9.3, 6.7 Hz, 4H), 1.97 (ddd, J=11.2, 8.6, 2.4 Hz, 1H), 1.74 (ddd, J 29.1, 10.8, 8.7 Hz, 2H), 1.04 (d, J 6.3 Hz, 5H).

Intermediates 2.2 and 2.3 were prepared in a similar manner as Intermediate 2.1, using the reagents provided in the table below in place of methyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylate (Compound 168).

Compound	Ester	Structure, Name and Data
Intermediate 2.2	Compound 35
		6-(3-(4-
		methoxybenzyl)ureido)spiro[3.3]heptane-
		2-carboxylic acid. LCMS-ESI (POS.) m/z:
		319.10 (M + H)+. 1H NMR (400 MHz,
		DMSO-d6) δ 12.00 (s, 1H), 7.15 (d, J = 8.1
		Hz, 2H), 6.87 (d, J = 8.1 Hz, 2H), 6.12 (s,
		2H), 4.09 (s, 2H), 3.91 (p, J = 8.3 Hz, 1H),
		3.73 (s, 3H), 2.92 (p, J = 8.5 Hz, 1H), 2.34
		(dt, J = 11.6, 6.3 Hz, 1H), 2.25-2.01 (m,
		5H), 1.75 (dt, J = 26.3, 9.8 Hz, 2H).
Intermediate 2.3	Intermediate 1.3
		6-(3-(4-
		fluorobenzyl)ureido)spiro[3.3]heptane-2-
		carboxylic acid. LCMS-ESI (POS.) m/z:
		307.10 (M + H)+. 1H NMR (400 MHz,
		DMSO-d6) δ 11.98 (s, 1H), 7.36 (d, J = 8.4
		Hz, 2H), 7.24 (d, J = 8.4 Hz, 2H), 6.26 (t, J =
		6.0 Hz, 1H), 6.18 (d, J = 8.0 Hz, 1H), 4.15
		(d, J = 6.1 Hz, 2H), 3.91 (q, J = 8.1 Hz, 1H),
		3.20 (s, 1H), 2.40 (d, J = 24.9 Hz, 2H), 2.14
		(dd, J = 19.9, 9.0 Hz, 4H), 2.01 (t, J = 10.0
		Hz, 1H), 1.88-1.77 (m, 1H), 1.71 (t, J = 9.8
		Hz, 1H).
2.6	Intermediate 1.16
		5-(3-(4-chlorobenzyl)ureido)pentanoic
		acid. LCMS-ESI (POS.) m/z: 285.1
		(M + H)+. 1H NMR (400 MHz, DMSO-d6) δ
		11.96 (s, 1H), 7.36 (d, J = 8.4 Hz, 2H), 7.25
		(d, J = 8.3 Hz, 2H), 6.33 (s, 1H), 5.97 (s,
		1H), 4.25-4.13 (m, 2H), 3.00 (t, J = 6.8 Hz,
		2H), 2.21 (t, J = 7.3 Hz, 2H), 1.58-1.43 (m,
		2H), 1.43-1.31 (m, 2H).
2.7	Intermediate 1.17
		6-(3-(4-chlorobenzyl)ureido)hexanoic
		acid. LCMS-ESI (POS.) m/z: 299.1
		(M + H)+. 1H NMR (400 MHz, DMSO-d6) δ
		11.91, 7.37 (d, J = 8.4 Hz, 2H), 7.25 (d, J =
		8.4 Hz, 2H), 6.32 (s, 1H), 5.94 (s, 1H), 4.18
		(d, J = 4.9 Hz, 2H), 2.98 (d, J = 8.0 Hz, 2H),
		2.19 (t, J = 7.3 Hz, 2H), 1.49 (p, J = 7.5 Hz,
		2H), 1.37 (p, J = 6.9 Hz, 2H), 1.25 (tt, J =
		9.9, 5.8 Hz, 2H).

Example C

Synthesis of Intermediate 3.1

Preparation of 1-(4-Chlorobenzyl)-3-(2-azaspiro[3.3]heptan-6-yl)urea (Intermediate 3.1). TFA (100 mL) was added to a stirring solution of tert-butyl 6-(3-(4-chlorobenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxylate (Intermediate 1.5) (17.8 g, 46.9 mmol, 1 equiv) in CH₂Cl₂ (200 mL) at rt. After 1 h, solvent was removed by rotary evaporation, the crude oil was azeotroped with toluene (3×100 mL) and dried under high vacuum. The crude oil was suspended in MeOH (250 mL), IONAC Na-38 OH⁻ resin (50 g) was added, and the reaction stirred gently for 1 h. The reaction was then filtered through a pad of celite and solvent removed by rotary evaporation to give the product as a white solid (12.5 g, 95%). LRMS (APCI) m/z 280.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.32 (d, J=8.4 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.75 (s, 1H), 4.64 (s, 1H), 4.29 (d, J=4.3 Hz, 2H), 4.14 (s, 1H), 4.03 (d, J=4.8 Hz, 2H), 2.68 (dddd, J=17.8, 10.3, 7.7, 3.0 Hz, 2H), 2.32-2.24 (m, 2H), 2.22-2.13 (m, 1H).

Intermediates 3.2, 3.3, 3.4, 3.5, and 3.6 were prepared in a similar manner as Intermediate 3.1, using the reagents provided in the table below in place of tert-butyl 6-(3-(4-chlorobenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxylate (Compound 197).

Compound	Protected Intermediate	Structure, Name and Data
Intermediate 3.2	Compound 37
		1-(4-methoxybenzyl)-3-(2-azaspiro[3.3]heptan-
		6-yl)urea. LRMS (APCI) m/z 276.1 (M + H).
Intermediate 3.3	Intermediate 1.7
		4-((3-(2-azaspiro[3.3]heptan-6-
		yl)ureido)methyl)benzamide. LRMS (APCI)
		m/z 289 (M + H).
Intermediate 3.4	Compound 8
		tert-butyl (6-(3-(4-methoxybenzyl)ureido)
		spiro[3.3]heptan-2-yl)carbamate. LCMS-ESI
		(POS.) m/z: 294.10 (M + H)+. 1H NMR (400 MHz,
		DMSO-d6) δ 8.49-7.95 (m, 3H), 7.36 (d, J = 8.4
		Hz, 2H), 7.24 (d, J = 8.4 Hz, 2H), 7.11-6.64 (m,
		1H), 4.15 (s, 2H), 3.93 (p, J = 8.2 Hz, 1H), 3.51
		(pd, J = 7.9, 2.7 Hz, 1H), 2.33 (dtd, J = 11.7, 7.8,
		4.6 Hz, 2H), 2.26-2.03 (m, 4H), 1.82 (ddd, J =
		11.1, 8.6, 5.3 Hz, 2H).
Intermedate 3.5	Compound 151
		1-(4-chlorobenzyl)-3-((2r,4s)-6-
		azaspiro[3.4]octan-2-yl)urea. LRMS (APCI)
		m/z 294.1 (M + H). 1H NMR (400 MHz, DMSO-
		d6) δ 7.35 (d, J = 4.3 Hz, 2H), 7.25 (d, J = 4.5 Hz,
		2H), 6.41 (d, J = 5.1 Hz, 1H), 6.32 (dd, J = 7.8,
		3.6 Hz, 1H), 4.17 (s, 2H), 4.11-3.96 (m, 1H),
		3.03-2.93 (m, 2H), 2.88 (d, J = 3.6 Hz, 2H), 2.17
		(d, J = 9.1 Hz, 2H), 1.93-1.74 (m, 4H).
Intermediate 3.6	Compound 152
		1-(4-chlorobenzyl)-3-((2s,4r)-6-
		azaspiro[3.4]octan-2-yl)urea. LRMS (APCI)
		m/z 294.1 (M + H). 1H NMR (400 MHz, DMSO-
		d6) δ 7.36 (d, J = 8.4 Hz, 2H), 7.25 (d, J = 8.4 Hz,
		2H), 6.50-6.34 (m, 2H), 4.17 (d, J = 6.1 Hz,
		2H), 4.04 (q, J = 8.1 Hz, 2H), 3.14 (s, 2H), 3.10
		(t, J = 7.4 Hz, 2H), 2.37-2.25 (m, 2H), 1.95-
		1.82 (m, 4H), 1.06 (d, J = 6.6 Hz, 1H).
3.7	Intermediate 1.18
		1-(5-aminopentyl)-3-(4-chlorobenzyl)urea.
		LRMS (APCI) m/z 270.1 (M + H).
3.8	Intermediate 1.19
		1-(4-chlorobenzyl)-3-(4-(piperidin-4-
		yl)butyl)urea. LRMS (APCI) m/z 324.1 (M + H).
3.9	Intermediate 1.20
		1-(4-chlorobenzyl)-3-(4-(piperazin-1-
		yl)butyl)urea. LRMS (APCI) m/z 325.2 (M + H).
3.10	Intermediate 18.1
		1-(oxazol-5-ylmethyl)-3-(4-(piperidin-4-
		yl)butyl)urea. LRMS (APCI) m/z 281.2 (M + H).
3.11	Intermediate 18.2
		1-(4-methoxybenzyl)-3-(4-(piperidin-4-
		yl)butyl)urea. LRMS (APCI) m/z 320.2 (M + H).
3.12	Intermediate 18.3
		4-((3-(4-(piperidin-4-
		yl)butyl)ureido)methyl)benzamide. LRMS
		(APCI) m/z 333.2 (M + H).
3.13	Intermediate 18.4
		1-(4-(piperidin-4-yl)butyl)-3-(pyridin-4-
		ylmethyl)urea. LRMS (APCI) m/z 291.3
		(M + H).
3.14	Intermediate 18.5
		1-((1H-pyrazol-4-yl)methyl)-3-(4-(piperidin-4-
		yl)butyl)urea. LRMS (APCI) m/z 231.7 (M + H).
3.15	Interemeidate 1.21
		1-(oxazol-5-ylmethyl)-3-(4-(piperidin-4-
		yl)butyl-1,1-d2)urea. LRMS (APCI) m/z 283.1
		(M + H).

Example D

Synthesis of Intermediate 4.1

Preparation of (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl methanesulfonate (Intermediate 4.1)

Step 1: Preparation of 3-[6-(hydroxymethyl)spiro[3.3]heptan-2-yl]-1-[(4-methoxyphenyl)methyl]urea. To a solution of 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (2.0 g, 6.28 mmol, 1.0 equiv) in DCM (20 mL) was added triethylamine (2 equiv) followed by isobutylchloroformate dropwise at 0° C. The solution was stirred at rt and monitored by LCMS. After 1 h, the solution was cooled to 0° C. and the precipitate was filtered and rinsed with DCM. The crude (isobutyl carbonic) 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic anhydride was used directly in the next step (99% yield).

The crude anhydride from above was dissolved in THF (20 mL) and sodium borohydride (0.475 g, 12.6 mmol, 2.0 equiv) was added portion wise at rt. The solution was monitored by LCMS analysis. The solution was cooled to 0° C. and satd aqueous sodium carbonate solution (20 mL) was added and the solution was stirred vigorously for 10 mins. The organic layer was separated the aqueous layer was extracted with 30 mL of DCM. The combined organic layer was washed with brine, dried, filtered, and concentrated to provide the product as white foam (1.82 g, 92% yield). LCMS-APCI (POS.) m/z: 315.0 (M+H)+. 1H NMR (400 MHz, DMSO-d₆) δ 7.15 (dd, J=8.5, 1.7 Hz, 2H), 6.87 (dt, J=8.6, 2.3 Hz, 2H), 6.18-5.95 (m, 2H), 4.40 (td, J=5.4, 1.3 Hz, 1H), 4.09 (d, J=5.9 Hz, 2H), 3.91 (q, J=8.1 Hz, 1H), 3.82 (td, J=9.3, 7.3, 2.9 Hz, 1H), 3.31 (t, J=5.8 Hz, 3H), 2.83 (q, J=6.9, 4.7 Hz, 1H), 2.79-2.71 (m, 1H), 2.24-2.08 (m, 2H), 2.02 (t, J=9.1 Hz, 1H), 1.87 (t, J=9.9 Hz, 1H), 1.81-1.57 (m, 4H).

Step 2: Preparation of (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl methanesulfonate. NEt₃ (2.0 equiv) was added to a solution of 3-[6-(hydroxymethyl)spiro[3.3]heptan-2-yl]-1-[(4-methoxyphenyl)methyl]urea (1.8 g, 5.71 mmol, 1.0 equiv) in CH₂Cl₂ (0.33 M). The reaction was cooled to 0° C. and methanesulfonyl chloride (0.72 g, 0.31 mmol, 1.1 equiv) was added dropwise and stirred for 30 mins. The solution was cooled to 0° C. and satd aqueous ammonium chloride solution was added and the solution stirred vigorously for 10 mins. The organic layer was separated and the aqueous layer extracted with 10 mL of DCM. The combined organic layer was washed with brine, dried, filtered, and concentrated to provide the product as a white foam (1.96 g, 84% yield). LCMS-APCI (POS.) m/z: 384.0 (M+H). 1H NMR (400 MHz, DMSO-d₆) δ 7.21 (dd, J=8.2, 1.6 Hz, 2H), 6.94 (dt, J=8.2, 1.6 Hz, 2H), 6.24-6.00 (m, 2H), 5.44 (td, J=5.4 Hz, 1.3 Hz, 2H), 4.59 (td, J=5.2, 1.3 Hz, 1H), 3.91 (q, J=8.1 Hz, 1H), 3.31 (t, J=5.8 Hz, 3H), 2.83 (q, J=6.9, 4.7 Hz, 1H), 2.65 (s, 3H), 2.79-2.71 (m, 1H), 2.24-2.08 (m, 2H), 2.02 (t, J=9.1 Hz, 1H), 1.87 (t, J=9.9 Hz, 1H), 1.81-1.57 (m, 4H).

Example E

Synthesis of Intermediate 5.1

Preparation of N-(6-aminospiro[3.3]heptan-2-yl)benzamide hydrochloride (Intermediate 5.1)

Step 1: Preparation of tert-butyl (6-benzamidospiro[3.3]heptan-2-yl)carbamate. NEt₃ (670 mg, 6.628 mmol, 3 equiv) and benzoyl chloride (341.61 mg, 2.430 mmol, 1.1 equiv) were added to a stirring solution of tert-butyl N-[6-aminospiro [3.3]heptan-2-yl]carbamate (500.00 mg, 2.209 mmol, 1.0 equiv) in CH₂Cl₂ (5 mL) at 0° C. before the reaction was allowed to return to rt. After 2 h, the reaction was then quenched with H₂O (20 mL), extracted with CH₂Cl₂ (2×20 mL). Organics were combined, washed with sat sodium chloride (20 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product (850 mg) which was used in the next step without further purification. LRMS (APCI) m/z 275 (M+H−56).

Step 2: Preparation of N-(6-aminospiro[3.3]heptan-2-yl)benzamide hydrochloride. HCl (2.5 mL, 4M in dioxanes) was added to a stirring solution of tert-butyl N-[6-benzamidospiro[3.3]heptan-2-yl]carbamate (830 mg, 2.5 mmol, 1.0 equiv) in CH₂Cl₂ (10 mL) at rt. After 1 h, the reaction was concentrated by rotary evaporation to afford the crude product (620 mg) as a white solid which was used without further purification. LRMS (APCI) m/z 231 (M+H).

Example F

Synthesis of Intermediate 6.1

Preparation of N2-(pyridin-2-yl)spiro[3.3]heptane-2,6-diamine hydrochloride (Intermediate 6.1)

Step 1: Preparation of tert-butyl (6-(pyridin-2-ylamino)spiro[3.3]heptan-2-yl)carbamate. 2-Aminopyridine (200 mg, 2.1 mmol, 2.0 equiv) and TFA (243 mg, 2.1 mmol, 2 equiv) were added to a stirring solution of tert-butyl N-[6-oxospiro[3.3]heptan-2-yl]carbamate (240 mg, 1.1 mmol, 1.0 equiv) in DCE (10 mL) at rt. After 30 min, NaHB(OAc)₃ (677 mg, 3.2 mmol, 3.0 equiv) was added and the reaction stirred for 12 h. The reaction was quenched with H₂O (20 mL), extracted with CH₂Cl₂ (2×20 mL). Organics were combined, washed with sat sodium chloride (20 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product (380 mg) as a yellow solid which was used in the next step without further purification. LRMS (APCI) m/z 248 (M+H−56).

Step 2: Preparation of N2-(pyridin-2-yl)spiro[3.3]heptane-2,6-diamine hydrochloride. HCl (2.5 mL, 4M in dioxanes) was added to a stirring solution of tert-butyl N-[6-(pyridin-2-ylamino)spiro[3.3] heptan-2-yl]carbamate (360 mg, 1.187 mmol, 1.0 equiv) in CH₂Cl₂ (5 mL) at rt. After 2 h, the reaction was concentrated by rotary evaporation to afford the crude product (280 mg) as a white solid which was used without further purification. LRMS (APCI) m/z 204 (M+H).

Example G

Synthesis of Intermediate 7.1

Preparation of tert-butyl ((1r,3r)-3-(benzylcarbamoyl)cyclobutyl)carbamate (Intermediate

Step 1: Preparation of tert-butyl ((1r,3r)-3-(benzylcarbamoyl)cyclobutyl)carbamate. EDCI (670 mg, 3.49 mmol, 1.5 equiv) was added to a stirring solution of (1r,3r)-3-[(tert-butoxycarbonyl)amino] cyclobutane-1-carboxylic acid (500.00 mg, 2.323 mmol, 1.00 equiv) in pyridine (5 mL) at rt. After 5 min, benzylamine (298.50 mg, 2.786 mmol, 1.20 equiv) was added and the reaction stirred for rt for 1 h. The reaction was then quenched with H₂O (20 mL), extracted with EtOAc (2×20 mL). The reaction was then quenched with H₂O (20 mL) and extracted with EtOAc (2×20 mL). The organic layers were combined, washed with sat sodium chloride (20 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product (640 mg) which was used in the next step without further purification. LRMS (APCI) m/z 249 (M+H−56).

Step 2: Preparation of (1r,3r)-3-amino-N-benzylcyclobutane-1-carboxamide hydrochloride. HCl (2 mL, 4 M in dioxane) was added to a stirring solution of tert-butyl N-[(1r,3r)-3-(benzylcarbamoyl)cyclobutyl] carbamate (827 mg, 1.00 equiv) in CH₂Cl₂ (10 mL) at rt. After 1 h, the reaction was concentrated by rotary evaporation to give the crude product as a brown solid (640 mg) which was used in the next step without further purification. LRMS (APCI) m/z 241 (M+H).

Example H

Synthesis of Intermediate 8.1

Preparation of (6-amino-2-azaspiro[3.3]heptan-2-yl)(p-tolyl)methanone (Intermediate 8.1)

Step 1: Preparation of tert-butyl (2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)carbamate. HATU (6.88 g, 18.1 mmol, 1.5 equiv) was added to a stirring solution of tert-butyl (2-azaspiro[3.3]heptan-6-yl)carbamate hydrochloride (3 g, 12.1 mmol, 1 equiv), 4-methylbenzoic acid (2.46 g, 18.1 mmol, 1.5 equiv) and NEt₃ (4.9 mL, 36.2 mmol, 3 equiv) in DMF (100 mL) at rt. After 12 h, the reaction was poured into EtOAc (500 mL), washed with sat sodium bicarbonate (3×250 mL), brine (2×250 mL), dried over sodium sulfate, filtered through a pad of silica, and solvent removed by rotary evaporation to give the crude product as a white solid (3.6 g).

Step 2: (6-amino-2-azaspiro[3.3]heptan-2-yl)(p-tolyl)methanone. TFA (25 mL) was added to a stirring solution of tert-butyl (2-(4-methylbenzoyl)-2-azaspiro[3.3]heptan-6-yl)carbamate (1 g, 3.03 mmol, 1 equiv) in CH₂Cl₂ (50 mL) at rt. After 1 h, the solvent was removed by rotary evaporation, azeotroped with toluene (3×50 mL), and dried under high vacuum to give the crude product as a yellow oil which was used in the next step without further purification. LRMS (APCI) m/z 231.1 (M+H).

Example I

Synthesis of Compound 198 and Intermediate 9.2

Chiral resolution of tert-butyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)carbamate (Compound 8). The racemic tert-butyl 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)carbamate (25 g) Compound 8 was resolved by chiral SFC (Chiralpak AD-H, 20% co-solvent [EtOH w/0.25% isopropylamine] at 80 g/min) affording the two chiral fragments Compound 198 (9.4 g, 38%) and Intermediate 9.2 (12 g, 48%) as white solids. The absolute stereochemistry of each fragment was not confirmed. Compound 198 elutes first from SFC using stated conditions, followed by Intermediate 9.2. Absolute stereochemistry was not determined. Compound 8 elutes first from SFC using stated conditions, followed by Intermediate 9.2.

Compound 198: LRMS (APCI) m/z 294.1 (M+H-Boc). ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, J=8.4 Hz, 2H), 7.24 (d, J=8.4 Hz, 2H), 7.04 (d, J=8.0 Hz, 1H), 6.25 (t, J=6.1 Hz, 1H), 6.17 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.92 (h, J=8.2 Hz, 1H), 3.79 (q, J=8.3 Hz, 1H), 2.27 (dp, J=18.8, 6.3 Hz, 2H), 2.19-2.00 (m, 2H), 1.93-1.69 (m, 4H), 1.36 (s, 9H).

Intermediate 9.2 LRMS (APCI) m/z 294.1 (M+H-Boc). ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, J=8.4 Hz, 2H), 7.24 (d, J=8.4 Hz, 2H), 7.04 (d, J=7.8 Hz, 1H), 6.25 (t, J=6.1 Hz, 1H), 6.17 (d, J=8.1 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.92 (h, J=7.9 Hz, 1H), 3.79 (q, J=8.2 Hz, 1H), 2.27 (dp, J=18.9, 7.5, 6.2 Hz, 2H), 2.09 (tq, J=13.3, 6.1 Hz, 2H), 1.93-1.68 (m, 4H), 1.36 (s, 9H).

Example J

Synthesis of Intermediate 10.1

Preparation of 1-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea (Intermediate 10.1). Diisobutylaluminum hydride (25% in toluene, 10.1 g, 17.8 mmol, 3 equiv.) was added to a stirring solution of methyl 6-(3-(4-chlorobenzyl)ureido) spiro[3.3] heptane-2-carboxylate (2.0 g, 17.8 mmol, 1 equiv) in THF (100 mL) at rt. After 2 h, the reaction was quenched by addition of MeOH (50 mL) and silica before solvent was removed by rotary evaporation. Purification by silica chromatography (0->10% MeOH/CH₂Cl₂) as a white solid (1.5 g, 81%). LRMS (APCI) m/z 309.1 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.14 (d, J=8.6 Hz, 2H), 6.86 (d, J=8.6 Hz, 2H), 6.09 (t, J=5.9 Hz, 1H), 6.06 (d, J=8.1 Hz, 1H), 4.40 (t, J=5.2 Hz, 1H), 4.09 (d, J=5.9 Hz, 2H), 3.91 (h, J=8.2 Hz, 1H), 3.30 (dd, J=6.5, 5.3 Hz, 2H), 2.29 (ddd, J=10.6, 7.4, 5.3 Hz, 1H), 2.21 (dt, J=16.6, 8.2 Hz, 1H), 2.16-2.08 (m, 1H), 2.01 (td, J=9.6, 8.3, 3.0 Hz, 1H), 1.87 (ddd, J=11.2, 8.2, 3.0 Hz, 1H), 1.79-1.60 (m, 4H).

Intermediate 10.2 was prepared in a similar manner as Intermediate 10.1, using the reagents provided in the table below.

Intermediate	Ester	Structure, Name and Data
10.2	Compound 35
		1-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)-3-
		(4-methoxybenzyl)urea. LRMS (APCI) m/z
		305.2 (M + H).

Example K

Synthesis of Intermediate 11.1

Preparation of 1-(4-chlorobenzyl)-3-(6-formylspiro[3.3]heptan-2-yl)urea (Intermediate 11.1). Dess-Martin Periodinane (4.1 g, 9.72 mmol, 1 equiv) was added to a stirring solution of 1-(4-chlorobenzyl)-3-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)urea (3.0 g, 9.72 mmol, 1 equiv) in CH₂Cl₂ (100 mL) and acetonitrile (100 mL) at rt. After 2 h, the reaction was quenched with sat sodium thiosulfate (100 mL) and diluted to 700 mL with saturated sodium bicarbonate and stirred vigorously for 10 min. The reaction was then extracted with CH₂Cl₂ (3×500 mL), organic layers combined, dried over sodium sulfate, and solvent removed by rotary evaporation to give the crude product as a tan solid (2.5 g, 84%). LRMS (APCI) m/z 307.1 (M+H).

Example L

Synthesis of Intermediates 12.1 and 12.2

Preparation of 1-(6-(aminomethyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea (Intermediate 12.2)

Step 1: Preparation of 1-(6-(azidomethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea. Methanesulfonyl chloride (857 mg, 7.5 mmol, 1.1 equiv) was added to a stirring solution of 1-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (2.1 g, 6.8 mmol, 1 equiv) and NEt₃ (2.1 g, 20.4 mmol, 3 equiv) in CH₂Cl₂ (50 mL) at rt. After 2 h, the reaction was quenched with saturated sodium bicarbonate (250 mL), extracted with CH₂Cl₂ (3×250 mL), organics combined, dried over sodium sulfate, filtered, and solvent removed by rotary evaporation. The crude material was suspended in DMF (8 mL) before NaN₃ (0.66 g, 10.2 mmol, 1.5 equiv) added and the reaction heated to 70° C. for 12 h. The reaction was cooled to rt, poured into EtOAc (500 mL), washed with saturated sodium bicarbonate (3×400 mL), the organic layer died over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the desired product as a white solid (1.98 g, 87%). LRMS (APCI) m/z 334.1 (M+H).

Step 2: Preparation of 1-(6-(aminomethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea. PtO₂ (0.1 g, 0.449 mmol, 0.1 equiv) and 1-(6-(azidomethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (1.5 g, 4.5 mmol, 1 equiv) were suspended in MeOH (50 mL) at rt before being stirred under H₂ (80 psi) for 1 h. The reaction was then filtered through a pad of celite and solvent removed by rotary evaporation to give the desired product as a white semi-solid (1.3 g, 98%). LRMS (APCI) m/z 308.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.31 (d, J=7.8 Hz, 2H), 7.26 (d, J=7.9 Hz, 2H), 4.29 (d, J=8.7 Hz, 2H), 4.02 (t, J=8.1 Hz, 1H), 2.64 (d, J=7.0 Hz, 2H), 2.46 (t, J=7.8 Hz, 1H), 2.25 (ddd, J=24.0, 11.5, 6.4 Hz, 3H), 2.11-1.99 (m, 1H), 1.92-1.73 (m, 3H), 1.69 (dd, J=11.1, 7.4 Hz, 1H).

Example M

Synthesis of Intermediate 13.1 Preparation of 2-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)acetic acid (Example 13.1)

Step 1: Preparation of ethyl 2-(6-((tert-butoxycarbonyl)amino)spiro[3.3]heptan-2-ylidene)acetate. Ethyl 2-(diethoxyphosphoryl)acetate (4.9 g, 22.2 mmol, 1 equiv) was added to a stirring solution of LiCl (2.26 g, 53.3 mmol, 2.4 equiv) in THF (25 mL) at rt. After 10 min, DBU (7.43 g, 48.8 mmol, 2.2 equiv) was added and the reaction stirred for an additional 10 min. tert-Butyl (6-oxospiro[3.3]heptan-2-yl)carbamate (5.0 g, 22.2 mmol, 1 equiv) in THF (20 mL) was then added and the reaction stirred for 14 h. The reaction was concentrated by rotary evaporation and product isolated by silica chromotography (0->50% EtOAc/Hex) as a white solid (5.05 g, 77%). LRMS (APCI) m/z 296.1 (M+H). ¹H NMR (400 MHz, Chloroform-d) δ 5.62 (d, J=6.8 Hz, 1H), 4.66 (s, 1H), 4.22-4.10 (m, 2H), 4.05 (s, 1H), 3.13 (d, J=38.8 Hz, 2H), 2.84 (d, J=38.1 Hz, 2H), 2.57-2.37 (m, 2H), 1.94 (td, J=8.8, 4.2 Hz, 2H), 1.45 (s, 9H), 1.28 (t, J=6.9 Hz, 3H).

Step 2: Preparation of ethyl 2-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)acetate. Ethyl 2-(6-((tert-butoxycarbonyl)amino)spiro[3.3]heptan-2-ylidene)acetate (5.05 g, 17.1 mmol, 1 equiv) and PtO₂ (308 mg, 0.17 mmol, 1 equiv) were suspended in MeOH (150 mL) and stirred under H₂ (80 psi) for 1 h. The reaction then filtered through a pad of celite and solvent removed by rotary evaporation. The crude material was suspended in CH₂Cl₂ (20 mL) before HCl (4 M in dioxanes, 42 mL, 170.9 mmol, 10 equiv) was added and the reaction stirred at rt for 2 h. The solvent was removed by rotary evaporation and dried under high vacuum before being suspended in CH₂Cl₂ (100 mL), NEt₃ (3.46 g, 34.2 mmol, 2 equiv) and 1-chloro-4-(isocyanatomethyl)benzene (3 g, 18.0 mmol, 1.05 equiv) were added and the reaction stirred at rt. After 12 h, the reaction was concentrated by rotary evaporation and product isolated by silica chromotography (0->10% MeOH/CH₂Cl₂) as a white solid (6.3 g, 98%). LRMS (APCI) m/z 365.1 (M+H). ¹H NMR (400 MHz, Chloroform-d) δ 7.31 (s, 2H), 7.22 (d, J=8.0 Hz, 2H), 4.67 (t, J=6.0 Hz, 1H), 4.54 (d, J=7.3 Hz, 1H), 4.33 (d, J=5.9 Hz, 2H), 4.11 (q, J=7.1 Hz, 2H), 4.01 (q, J=7.8 Hz, 1H), 3.51 (d, J=5.1 Hz, 3H), 2.62-2.45 (m, 2H), 2.37 (d, J=7.9 Hz, 2H), 2.35-2.21 (m, 2H), 2.10 (ddd, J=11.9, 7.7, 4.1 Hz, 1H), 1.77 (dq, J=19.7, 10.6, 10.1 Hz, 4H), 1.67 (s, 2H), 1.30-1.20 (m, 3H), 1.09 (q, J=5.6 Hz, 1H).

Step 3: Preparation of 2-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)acetic acid. Ethyl 2-(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)acetate (6.3 g, 17.3 mmol, 1 equiv) and LiOH (827 mg, 34.5 mmol, 2 equiv) were suspended in MeOH/water (19 mL/1 mL) at rt. After 4 h, the MeOH was removed by rotary evaporation and the crude diluted with water (˜25 mL) before the product was precipitated by addition of 1 M HCl (˜20 mL). The resulting precipitate was collected by filtration, washed with water, and dried under high vacuum to give the desired product as a white solid (4.5 g, 77%). LRMS (APCI) m/z 337.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.39-7.15 (m, 4H), 4.37-4.18 (m, 2H), 4.01 (d, J=8.9 Hz, 1H), 2.49 (pd, J=11.3, 7.6, 5.9 Hz, 2H), 2.31 (dq, J=36.6, 6.3 Hz, 4H), 2.10 (d, J=10.4 Hz, 1H), 1.77 (ddt, J=36.3, 19.2, 10.0 Hz, 4H).

Intermediate 13.2 was prepared in a similar manner as Intermediate 13.1, using the reagents provided in the table below.

Intermediate	Phosphonate	Structure, Name and Data
13.2	ethyl 2- (diethoxyphosphoryl)pro- panoate
		2-(6-(3-(4-
		chlorobenzyl)ureido)spiro[3.3]heptan-2-
		yl)propanoic acid. LRMS (APCI) m/z 351.1
		(M + H).

Example N

Synthesis of Intermediate 14.1

Preparation of 1-(6-acetylspiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (Intermediate 14.1)

Step 1: Preparation of 6-(3-(4-chlorobenzyl)ureido)-N-methoxy-N-methylspiro[3.3]heptane-2-carboxamide. HATU (6.48 g, 17.0 mmol, 1.1 equiv) was added to a stirring solution of 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (5.0 g, 15.5 mmol, 1 equiv), N,O-dimethylhydroxylamine (3 g, 31.0 mmol, 2 equiv), and NEt₃ (6.3 g, 61.96 mmol, 4 equiv) in EtOAc (30 mL) and iPOH (10 mL) at rt. After 12 h, silica was added and solvent removed by rotary evaporation before the product was isolated by silica chromatography (0->10% MeOH/CH2Cl2) as a glassy solid (5.6 g, 98%). LRMS (APCI) m/z 366.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.32 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.03 (p, J=8.0 Hz, 1H), 3.69 (s, 3H), 3.44 (d, J=14.8 Hz, 1H), 3.18 (s, 3H), 2.54 (ddd, J=11.7, 7.2, 5.2 Hz, 1H), 2.35-2.27 (m, 3H), 2.27-2.20 (m, 1H), 2.11 (t, J=9.8 Hz, 1H), 1.93 (dd, J=11.0, 8.5 Hz, 1H), 1.83 (dd, J=11.4, 8.7 Hz, 1H).

Step 2: Preparation of 1-(6-acetylspiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea. MeMgBr (3 M in THF, 15.4 mL, 46.4 mmol, 3 equiv) was added dropwise to a stirring solution of 6-(3-(4-chlorobenzyl)ureido)-N-methoxy-N-methylspiro[3.3]heptane-2-carboxamide (5.6 g, 15.5 mmol, 1 equiv) in THF (150 mL) at 0° C. After 1 h, the reaction was quenched with saturated sodium bicarbonate (500 mL), extracted with CH₂Cl₂ (3×250 mL), organics combined, dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the desired compound as a white solid. LRMS (APCI) m/z 321. (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, J=8.3 Hz, 2H), 7.24 (d, J=8.2 Hz, 2H), 6.26 (t, J=6.1 Hz, 1H), 6.18 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.90 (q, J=8.1 Hz, 1H), 3.15 (p, J=8.6 Hz, 1H), 2.34 (ddd, J=10.6, 7.3, 5.3 Hz, 1H), 2.23-1.96 (m, 8H), 1.86-1.64 (m, 2H).

Example O

Synthesis of Intermediate 15.1

Preparation of 1-(6-(1-aminoethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (Intermediate 15.1)

Step 1: Preparation of 1-(4-chlorobenzyl)-3-(6-(1-hydroxyethyl)spiro[3.3]heptan-2-yl)urea. LiBH₄ (1 M in THF, 468 μL, 0.468 mmol, 0.5 equiv) was added to a stirring solution of 1-(6-acetylspiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (300 mg, 0.935 mmol, 1 equiv) in THF (10 mL) at rt. After 1 h, the reaction was quenched with MeOH (10 mL) and silica before solvent was removed by rotary evaporation. The product was then isolated by silica chromatography (0->15% MeOH/CH₂Cl₂) as a white solid (300 mg, 99%). LRMS (APCI) m/z 323.1 (M+H). ¹H NMR (400 MHz, Chloroform-d) δ 7.31 (d, J=8.4 Hz, 2H), 7.23 (d, J=8.3 Hz, 2H), 4.61 (s, 1H), 4.50 (t, J=6.4 Hz, 1H), 4.34 (d, J=5.8 Hz, 2H), 4.02 (q, J=7.9, 7.3 Hz, 1H), 3.65 (d, J=5.8 Hz, 1H), 3.51 (d, J=5.1 Hz, 2H), 2.56-2.43 (m, 1H), 2.31 (td, J=11.6, 4.8 Hz, 1H), 2.21-2.03 (m, 2H), 1.90-1.69 (m, 4H), 1.08 (dd, J=6.2, 3.0 Hz, 3H).

Step 2: Preparation of 1-(6-(1-azidoethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea. DIAD (376 mg, 1.86 mmol, 1.5 equiv) was added to a stirring solution of triphenylphosphine (1.2 g, 1.86 mmol, 1.5 equiv) in THF at 0° C. After 10 min, DPPA (682 mg, 2.48 mmol, 2 equiv) and 1-(4-chlorobenzyl)-3-(6-(1-hydroxyethyl)spiro[3.3]heptan-2-yl)urea (400 mg, 1.24 mmol, 1 equiv) were added and the reaction stirred for 14 h while returning to rt. Solvent was removed by rotary evaporation and product isolated by silica chromatography (0->100% EtOAc/hexanes) as a white solid (350 mg, 81%). LRMS (APCI) m/z 348.1 (M+H).

Step 3: Preparation of 1-(6-(1-aminoethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea. 1-(6-(1-Azidoethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (800 mg, 2.3 mmol, 1 equiv) and PtO₂ (52 mg, 0.23 mmol, 0.1 equiv) were suspended in MeOH (25 mL) before being stirred under H₂ (80 psi) for 1 h. The reaction was filtered through a pad of celite and solvent removed by rotary evaporation to give the product as a sticky semi-solid (740 mg, 99%). LRMS (APCI) m/z 322.1 (M+H).

Example P

Synthesis of Intermediate 16.1

Preparation of 1-(4-chlorobenzyl)-3-(6-((methylamino)methyl)spiro[3.3]heptan-2-yl)urea (Intermediate 16.1)

Step 1: Preparation of N-((6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)formamide. Formic acid (61 mg, 1.34 mmol, 2.3 equiv) and acetic anhydride (77 mg, 0.755 mmol, 1.3 equiv) were heated to 60° C. for 2 h. The reaction was then cooled to rt before 1-(6-(aminomethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (200 mg, 0.581 mmol, 1 equiv) and DIPEA (300 mg, 2.32 mmol, 4 equiv) were added. After 2 h, the reaction was quenched with MeOH, concentrated by rotary evaporation, and dried under high vacuum. LRMS (APCI) m/z 336.2 (M+H).

Step 2: Preparation of 1-(4-chlorobenzyl)-3-(6-((methylamino)methyl)spiro[3.3]heptan-2-yl)urea. N-((6-(3-(4-Chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)methyl)formamide (138 mg, 0.412 mmol, 1 equiv) in THF (500 μL) was added dropwise to a stirring solution of BH₃ (dimethylsulfide complex, 2M in THF, 0.791 mL, 1.58 mmol, 4 equiv) at 0° C. before being allowed to return to rt. After 2 h, the reaction was quenched with MeOH and concentrated by rotary evaporation. The resulting oil was suspended in HCl (4 M in dioxanes, 5 mL), concentrated by rotary evaporation. The residue was triturated with EtOAc and resultant solid dried under high vacuum to give the product as a white solid (163 mg, 115%). LRMS (APCI) m/z 322.2 (M+H).

Example Q

Synthesis of Intermediate 17.1

Preparation of 6-((2-fluorophenyl)(methyl)amino)-6-oxohexan-1-aminium chloride (Intermediate 17.1)

Step 1: tert-butyl (6-((2-fluorophenyl)(methyl)amino)-6-oxohexyl)carbamate. HATU (6.56 g, 17.2 mmol, 2 equiv) was added to a stirring solution of 6-((tert-butoxycarbonyl)amino)hexanoic acid (2 g, 8.6 mmol, 1 equiv), 2-fluoro-N-methylaniline (1.62 g, 12.9 mmol, 1.5 equiv), and DIPEA (3.34 g, 25.9 mmol, 3 equiv) in DMF (15 mL) at rt. After 72 h, the reaction was poured into water (200 mL), extracted with EtOAc (3×75 mL), organics combined, washed with ammonium chloride (3×50 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation. The resultant oil was filtered through a plug of silica to yield the product as an amber oil (2.5 g, 85%). LRMS (APCI) m/z 339.1 (M+H).

Step 2: 6-((2-fluorophenyl)(methyl)amino)-6-oxohexan-1-aminium chloride. HCl (4M in dioxanes, 15 mL, 60 mmol, 10 equiv) was added to a stirring solution of tert-butyl (6-((2-fluorophenyl)(methyl)amino)-6-oxohexyl)carbamate (2.1 g, 6.2 mmol, 1 equiv) in MeOH (100 mL) at rt. After 4 h, solvent was removed by rotary evaporation and dried under high vacuum to give the product as a white solid (1.5 g, 101%). LRMS (APCI) m/z 239.1 (M+H).

Example R

Synthesis of Intermediate 18.1

Preparation of 6-((2-fluorophenyl)(methyl)amino)-6-oxohexan-1-aminium chloride (Intermediate 18.1)

Step 1: tert-butyl 4-(4-isocyanatobutyl)piperidine-1-carboxylate. Triphosgene (926 mg, 3.12 mmol, 0.4 equiv) was added to a vigiously stirring solution of tert-butyl 4-(4-aminobutyl)piperidine-1-carboxylate (2 g, 7.8 mmol, 1 equiv) in saturated sodium bicarbonate (30 mL) and CH₂Cl₂ (30 mL) at 0° C. After 15 min, the organic layer was removed, aqueous later extracted with CH₂Cl₂ (3×30 mL), organic layers combined, dried over sodium sulfate, and filtered. The isocyanate solution was split and used in subsequent steps without further purification.

Step 2: tert-butyl 4-(4-(3-(oxazol-5-ylmethyl)ureido)butyl)piperidine-1-carboxylate. Oxazol-5-ylmethanamine (152 mg, 1.56 mmol, 1 equiv) was added to a stirring solution of tert-butyl 4-(4-isocyanatobutyl)piperidine-1-carboxylate (441 mg, 1.56 mmol, 1 equiv) in CH₂Cl₂ (5 mL) and saturated sodium bicarbonate (3 mL) at rt. After 4 h, the organic layer was separated and filtered through a pad of silica, washed with 5% MeOH/CH₂Cl₂ (20 mL), and solvent removed by rotary evaporation to give the crude product (459 mg, 44%) which was used without further purification. LRMS (APCI) m/z 381.2 (M+H).

Intermediates 18.2-18.5 were prepared in a similar manner as Intermediate 18.1, using the reagents provided in the table below.

Intermediate	Amine	Structure, Name and Data
18.2	(4- methoxyphenyl)methanamine
		tert-butyl 4-(4-(3-(4-
		methoxybenzyl)ureido)butyl)piperidine-1-
		carboxylate. LRMS (APCI) m/z 420.2.1 (M + H).
18.3	4-(aminomethyl)benzamide
		tert-butyl 4-(4-(3-(4-
		carbamoylbenzyl)ureido)butyl)piperidine-1-
		carboxylate. LRMS (APCI) m/z 433.21 (M + H).
18.4	pyridin-4-ylmethanamine
		tert-butyl 4-(4-(3-(pyridin-4-
		ylmethyl)ureido)butyl)piperidine-1-
		carboxylate. LRMS (APCI) m/z 391.3 (M + H).
18.5	(1H-pyrazol-4- yl)methanamine
		tert-butyl 4-(4-(3-((1H-pyrazol-4-
		yl)methyl)ureido)butyl)piperidine-1-
		carboxylate. LRMS (APCI) m/z 380.2 (M + H).

Example S

Synthesis of Intermediate 19.1

Preparation of (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl 4-methylbenzenesulfonate (Intermediate 19.1). 4-Methylbenzenesulfonyl chloride (532 mg, 2.79 mmol, 1.25 equiv) was added to a stirring solution of 1-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea (Intermediate 10.1, 680 mg, 2.23 mmol, 1 equiv) and triethylamine (452 mg, 4.47 mmol, 2 equiv) in CH₂Cl₂ (25 mL) at rt. After 12 h, the reaction was quenched with saturated sodium bicarbonate (100 mL), extracted with CH₂Cl₂ (3×100 mL), organics combined, dried over sodium sulfate, filtered, and solvent removed by rotary evaporation. LRMS (APCI) m/z 459.1 (M+H). ¹H NMR (400 MHz, Chloroform-d) δ 7.79 (d, J=8.2 Hz, 2H), 7.36 (d, J=7.8 Hz, 2H), 7.22 (d, J=8.2 Hz, 2H), 6.91-6.81 (m, 2H), 4.57 (t, J=5.6 Hz, 1H), 4.47 (d, J=7.4 Hz, 1H), 4.28 (d, J=5.5 Hz, 2H), 4.00 (d, J=7.0 Hz, 2H), 3.94 (d, J=6.6 Hz, 2H), 3.81 (s, 3H), 2.47 (s, 3H), 2.47-2.40 (m, 1H), 2.27 (dt, J=12.1, 6.3 Hz, 1H), 2.11 (ddd, J=11.7, 8.4, 3.4 Hz, 1H), 1.98 (td, J=10.0, 8.3, 2.8 Hz, 1H), 1.80-1.71 (m, 4H).

Intermediate 19.2 was prepared in a similar manner as Intermediate 19.1, using the reagents provided in the table below.

Intermediate	Alcohol	Structure, Name and Data
19.2	Intermediate 10.2
		(6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptan-
		2-yl)methyl 4-methylbenzenesulfonate. LRMS
		(APCI) m/z 463.2 (M + H).

Example T

Synthesis of Intermediate 20.1

Preparation of tert-butyl 4-(4-aminobutyl-4,4-d2)piperidine-1-carboxylate (Intermediate 20.1)

Step 1: tert-butyl 4-(4-hydroxybutyl-4,4-d2)piperidine-1-carboxylate. To a solution of 4-[1-(tert-butoxycarbonyl)piperidin-4-yl]butanoic acid (1 g, 3.685 mmol, 1 equiv) in THF (15 mL) at 0° C. was added LiAlD₄ (4.4 mL, 1 mol/L, 1.20 equiv) dropwise under nitrogen atmosphere. After stirred at 0° C. for 2 h under nitrogen atmosphere, the reaction was determined by LCMS. The mixture was adjusted to pH 8 with KOH(aq.) and filtered to remove solids. The filtrate was dried over anhydrous Na₂SO₄ and concentrated under reduced pressure to afford the product (860 mg) as a white oil. LRMS (APCI) m/z 204 [M+H−56].

Step 2: tert-butyl 4-(4-((methylsulfonyl)oxy)butyl-4,4-d2)piperidine-1-carboxylate. To a solution of tert-butyl 4-[4-hydroxy(4,4-2H2)butyl]piperidine-1-carboxylate (800 mg, 3.084 mmol, 1 equiv) in DCM (10 mL) at 0° C. were added methanesulfonyl chloride (526 mg, 4.59 mmol, 1.5 equiv) and triethylamine (621 mg, 6.14 mmol, 1.99 equiv). After stirred at r.t. for 2 h, to the resulting mixture was added water (20 mL), extracted with CH₂Cl₂ (3×30 mL). The combined organic layers were washed with brine (2×30 mL), dried over anhydrous Na₂SO₄, concentrated under reduced pressure to afford the product (1 g) as a yellow oil. LRMS (APCI) m/z 282 [M+H−56].

Step 3: tert-butyl 4-(4-(1,3-dioxoisoindolin-2-yl)butyl-4,4-d2)piperidine-1-carboxylate. To a solution of tert-butyl 4-[4-(methanesulfonyloxy)(4,4-2H2)butyl]piperidine-1-carboxylate (1.0 g, 2.96 mmol, 1 equiv) in MeCN (15 mL) at r.t. was added 2-potassioisoindole-1,3-dione (0.83 g, 4.48 mmol, 1.5 equiv). After being stirred at 80° C. overnight, the resulting mixture was cooled to r.t., added water (30 mL), extracted with CH₂Cl₂ (3×30 mL). The combined organic layers were washed with brine (2×30 mL), dried over anhydrous Na₂SO₄. After filtration, the filtrate was concentrated under reduced pressure to afford the product (1 g) as a yellow oil. LRMS (APCI) m/z 333 [M+H−56].

Step 4: tert-butyl 4-(4-aminobutyl-4,4-d2)piperidine-1-carboxylate. To a solution of tert-butyl 4-[4-(1,3-dioxoisoindol-2-yl)(4,4-2H2)butyl]piperidine-1-carboxylate (1.0 g, 2.57 mmol, 1 equiv) in ethyl alcohol (10 mL) at r.t. was added hydrazine monohydrate (642 mg, 13.1 mmol, 5.1 equiv). After being stirred at 80° C. overnight, the mixture was cooled to r.t. and filtered to remove solids. The filtrate was concentrated under reduced pressure to afford the product (630 mg) as a yellow semi-solid. LRMS (ES) m/z 203[M+H−56].

Example U

Synthesis of Intermediate 21.1

Preparation of oxazol-5-ylmethan-d2-amine (Intermediate 21.1). To a solution of oxazole-5-carbonitrile (188 mg, 2.00 mmol, 1.0 equiv) in THF (6 mL) was added LiAlD₄ (84 mg, 2.00 mmol, 1.0 equiv) as solid. The mixture was vigorously stirred at 23° C. for 3 h. Upon completion, Na₂SO₄·10H₂O was added carefully to quench the reaction until gas evolution ceased. The solid was filtered off and the filtrate was concentrated to yield the crude oxazol-5-ylmethan-d₂-amine (90 mg, 45%), which was used directly without further purification. LRMS (APCI+) m/z 101.2 (M+H).

Example V

Synthesis of Intermediates 22.1

Preparation of 6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-amine (Intermediate 22.1)

Step 1: tert-butyl (6-hydroxy-6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate. To a solution of diisopropylamine (303 mg, 3.00 mmol, 2.25 equiv) in THF (5 mL) was added n-BuLi (2.5 M in hexanes, 1.17 mL, 2.93 mmol, 2.2 equiv) at −30° C. The solution was slightly warmed to −10° C. over 20 min. Then the freshly prepared LDA solution was cooled down to −78° C., followed by the dropwise addition of a THF solution (1 mL) of 4-picoline (273 mg, 2.93 mmol, 2.2 equiv). The deprotonation was kept at this temperature for 1 h. Then a solution of tert-butyl (6-oxospiro[3.3]heptan-2-yl)carbamate (300 mg, 1.33 mmol, 1.0 equiv) in THF (2 mL) was added at −78° C. over 1 min. The reaction was then allowed to warm to 23° C. over 2 h and it was further stirred at this temperature for 1 h. Upon completion, half-saturated NH₄Cl solution was added to quench the reaction. The aqueous phase was extracted by EtOAc (5 mL×2). The combined organic phase was washed with brine, dried (MgSO₄), filtered, and concentrated to yield the crude tert-butyl (6-hydroxy-6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate. LRMS (APCI+) m/z 319.1 (M+H).

Step 2: tert-butyl (6-(pyridin-4-ylmethylene)spiro[3.3]heptan-2-yl)carbamate. To a solution of the crude tert-butyl (6-hydroxy-6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate (up to 1.33 mmol, 1.0 equiv) in CH₂Cl₂ (2 mL) was added Et₃N (269 mg, 2.66 mmol, 2.0 equiv) and MsCl (183 mg, 1.60 mmol, 1.2 equiv). The reaction was stirred at 23° C. for 2 h. Upon completion, volatiles were removed in vacuo and PhMe (1.5 mL) was added, followed by DBU (1.01 g, 6.65 mmol, 5.0 equiv). The mixture was heated at 60° C. for 14 h. Upon completion, the reaction was then poured into a mixture of half-saturated brine (10 mL) and EtOAc (10 mL). The aqueous phase was extracted by EtOAc (5 mL×2). The combined organic phase was washed with brine, dried (MgSO₄), filtered, concentrated, and purified by flash column chromatography (silica, hexanes/EtOAc) to yield tert-butyl (6-(pyridin-4-ylmethylene)spiro[3.3]heptan-2-yl)carbamate (241 mg, 60% yield over 2 steps) as a colorless oil. LRMS (APCI+) m/z 301.1 (M+H).

Step 3: tert-butyl (6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate. To a solution of tert-butyl (6-(pyridin-4-ylmethylene)spiro[3.3]heptan-2-yl)carbamate (240 mg, 0.80 mmol, 1.0 equiv) in THF/MeOH (6 mL, 2:1) was added Pd/C (10% wt. loading, 30% mass equiv). The mixture was bubbled through H₂ gas for 3 min and then stirred under 1 atm H₂ atmosphere for 14 h at 23° C. Upon completion, solid was filtered off and the filtrate was concentrated to yield the crude tert-butyl (6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate which was directly subjected to next step. LRMS (APCI+) m/z 303.1 (M+H).

Step 4: 6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-amine. To a solution of the crude tert-butyl (6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)carbamate (up to 0.80 mmol) in CH₂Cl₂ (3 mL) was added TFA (0.5 mL) at 23° C. The mixture was stirred at this temperature for 3 h. Upon completion, volatiles were removed in vacuo to yield the crude 6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-amine (Intermediate 22.1, 150 mg, 93%) which was directly used without further purifications. LRMS (APCI+) m/z 203.1 (M+H).

Example W

Synthesis of Intermediate 23.1

Preparation of 6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-amine (Intermediate 23.1)

Step 1: tert-butyl (6-(2-(6-methylnicotinoyl)hydrazine-1-carbonyl)spiro[3.3]heptan-2-yl)carbamate. To a solution of 6-((tert-butoxycarbonyl)amino)spiro[3.3]heptane-2-carboxylic acid (180 mg, 0.71 mmol, 1.0 equiv) in DMF (2 mL) was added 6-methylnicotinohydrazide (107 mg, 0.71 mmol, 1.0 equiv) and HATU (280 mg, 0.78 mmol, 1.1 equiv), followed by DIPEA (215 mg, 2.12 mol, 3.0 equiv). The reaction was stirred at 23° C. for 14 h. Upon completion, EtOAc (5 mL) was added. The organic phase was washed by brine, dried (MgSO₄), filtered, and concentrated to yield the crude tert-butyl (6-(2-(6-methylnicotinoyl)hydrazine-1-carbonyl)spiro[3.3]heptan-2-yl)carbamate which was directly used in the next step without further purification. LRMS (APCI+) m/z 389.1 (M+H).

Step 2: tert-butyl (6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)carbamate. To a solution of the crude tert-butyl (6-(2-(6-methylnicotinoyl)hydrazine-1-carbonyl)spiro[3.3]heptan-2-yl)carbamate (0.71 mmol, 1.0 equiv) in THF (2 mL) was added Triphenylphosphine (223 mg, 0.85 mmol, 1.2 equiv), imidazole (145 mg, 2.12 mmol, 3.0 equiv), tetrabromomethane (259 mg, 0.78 mmol, 1.1 equiv) equentially. The reaction was stirred at 23° C. for 16 h. Upon completion, a mixed solution of NaHCO₃ and Na₂S₂O₃ was added to quench the reaction. The aqueous phase was extracted by CH₂Cl₂ (5 mL×3). The combined organic phase was washed by brine, dried (MgSO₄), filtered, concentrated, and purified by flash column chromatography (silica, CH₂Cl₂/MeOH) to yield tert-butyl (6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)carbamate (148 mg, 57% over 2 steps) as a white solid. LRMS (APCI+) m/z 371.1 (M+H).

Step 3: 6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-amine. To a solution of tert-butyl (6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)carbamate (74 mg, 0.20 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added HCl (4 M in 1,4-dioxane, 0.40 mL, 1.60 mmol, 8.0 equiv). The mixture was stirred at 23° C. for 20 h. Upon completion, the volatile was removed in vacuo to yield the crude 6-(5-(6-methylpyridin-3-yl)-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-amine (intermediate 23.1, 52 mg, 96%) as a white waxy solid which was directly used without further purifications. LRMS (APCI+) m/z 271.1 (M+H).

Example X

Synthesis of Intermediate 24.1

Preparation of 6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-amine (Intermediate 24.1)

Step 1: tert-butyl (6-(pyrimidin-2-ylmethylene)spiro[3.3]heptan-2-yl)carbamate. To a vial charged with 2-(chloromethyl)pyrimidine HCl salt (495 mg, 3.00 mmol, 1.0 equiv) was added triphenylphosphine (787 mg, 3.00 mmol, 1.0 equiv) and toluene (2 mL). The mixture was stirred at 100° C. for 16 h. Then solvent was decanted and residue was dried to yield the crude triphenyl(pyrimidin-2-yl-methyl)phosphonium chloride. To the crude ylide was added DMSO (2 mL), followed by sodium tert-butoxide (577 mg, 6.00 mmol, 2.0 equiv) at 23° C. The reaction was stirred at this temperature for 1 h, followed by the addition of tert-butyl (6-oxospiro[3.3]heptan-2-yl)carbamate (676 mg, 3.00 mmol, 1.0 equiv). The dark brownish mixture was stirred at 23° C. for 18 h before it was poured into a mixture of half-saturated NH₄Cl solution (10 mL) and CH₂Cl₂ (10 mL). The layers were separated and the aqueous phase was extracted by CH₂Cl₂ (5 mL×2). The combined organic phase was washed by brine, dried (MgSO₄), filtered, concentrated, and purified by flash column chromatography (silica, CH₂Cl₂/MeOH) to yield tert-butyl (6-(pyrimidin-2-ylmethylene)spiro[3.3]heptan-2-yl)carbamate (250 mg, 28% yield) as a yellowish gum. LRMS (APCI+) m/z 302.1 (M+H).

Step 2: tert-butyl (6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-yl)carbamate. To a vial charged with yield tert-butyl (6-(pyrimidin-2-ylmethylene)spiro[3.3]heptan-2-yl)carbamate (250 mg, 0.83 mmol, 1.0 equiv), piperidine (74 mg, 0.87 mmol, 1.05 equiv), formic acid (40 mg, 0.87 mmol, 1.05 equiv), Pd/C (10% wt. loading, 20% mass equiv), and EtOH (3 mL). The mixture was stirred at 75° C. for 6 h. Upon completion, solid was filtered off and the filtrate was concentrated and purified by flash column chromatography (silica, CH₂Cl₂/MeOH) to yield tert-butyl (6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-yl)carbamate (142 mg, 56% yield) as a light yellowish gum. LRMS (APCI+) m/z 304.2 (M+H).

Step 3: 6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-amine. To a solution of tert-butyl (6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-yl)carbamate (142 mg, 0.47 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added HCl (4 M in 1,4-dioxane, 0.93 mL, 3.74 mmol, 8.0 equiv). The mixture was stirred at 23° C. for 20 h. Upon completion, the volatile was removed in vacuo to yield the crude 6-(pyrimidin-2-ylmethyl)spiro[3.3]heptan-2-amine (Intermediate 24.1, 95 mg, 99%) as a light yellowish gum which was directly used without further purifications. LRMS (APCI+) m/z 204.1 (M+H).

Example Y

Synthesis of Intermediate 25.1

Preparation of 6-(pyridin-4-yloxy)spiro[3.3]heptan-2-amine (Intermediate 25.1)

Step 1: tert-butyl (6-(pyridin-4-yloxy)spiro[3.3]heptan-2-yl)carbamate. To a vial charged with tert-butyl N-{6-hydroxyspiro[3.3]heptan-2-yl}carbamate (227 mg, 1.00 mmol, 1.0 equiv), triphenylphosphine (393 mg, 1.50 mmol, 1.5 equiv), 4-hydroxypyridine (142 mg, 1.50 mmol, 1.5 equiv) was added toluene (3 mL), followed by diisopropyl azodicarboxylate (DIAD, 303 mg, 1.50 mmol, 1.5 equiv). The reaction was then stirred at 80° C. for 3 h. Upon completion, the reaction was directly concentrated and purified by reverse-phase column chromatography (H₂O (0.1% HCO₂H)/MeCN (0.1% HCO₂H)) to yield tert-butyl (6-(pyridin-4-yloxy)spiro[3.3]heptan-2-yl)carbamate (166 mg, 54%) as a colorless oil. LRMS (APCI+) m/z 305.1 (M+H).

Step 1: 6-(pyridin-4-yloxy)spiro[3.3]heptan-2-amine. To a solution of tert-butyl (6-(pyridin-4-yloxy)spiro[3.3]heptan-2-yl)carbamate (166 mg, 0.545 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added HCl (4 M in 1,4-dioxane, 1.09 mL, 4.36 mmol, 8.0 equiv). The mixture was stirred at 23° C. for 20 h. Upon completion, the volatile was removed in vacuo to yield the crude 6-(pyridin-4-yloxy)spiro[3.3]heptan-2-amine (Intermediate 25.1, 110 mg, 98%) as a light yellowish gum which was directly used without further purifications. LRMS (APCI+) m/z 205.1 (M+H).

Intermediate 25.2 was prepared in a similar manner as Intermediate 25.1, using the reagents provided in the table below.

Inter-
mediate	Phenol	Structure, Name and Data
25.2	3-hydroxypyridine
		6-(pyridin-3-yloxy)spiro[3.3]heptan-2-amine.
		LRMS (APCI) m/z 205.1 (M + H).

Example Z

Synthesis of Intermediates 26.1

Preparation of 6-(methylsulfonyl)spiro[3.3]heptan-2-amine (Intermediate 26.1)

Step 1: tert-butyl (6-(methylthio)spiro[3.3]heptan-2-yl)carbamate. To a solution of tert-butyl N-{6-hydroxyspiro[3.3]heptan-2-yl}carbamate (227 mg, 1.00 mmol, 1.0 equiv) in CH₂Cl₂ (3 mL) was added Et₃N (202 mg, 2.00 mmol, 2.0 equiv) and TsCl (229 mg, 1.20 mmol, 1.2 equiv) at 23° C. The mixture was stirred at 23° C. for 3 h before it was poured into a half-saturated NaHCO₃ solution. The aqueous phase was extracted by CH₂Cl₂ (5 mL×2) and the combined organic phase was washed by brine, dried (MgSO₄), filtered, concentrated, and purified by flash column chromatography (silica, hexanes/EtOAc) to yield the desired tosylate. Next, to a suspension of the tosylate obtained above in EtOH (3 mL) was added sodium thiomethoxide (210 mg, 3.00 mmol, 3.0 equiv). The mixture was stirred at 60° C. for 18 h. Upon completion, the reaction was quenched by half-saturated NH₄Cl solution. The aqueous phase was extracted by EtOAc (5 mL×2). The combined organic phase was washed by brine, dried (MgSO₄), filtered, and concentrated to yield the crude tert-butyl (6-(methylthio)spiro[3.3]heptan-2-yl)carbamate (183 mg, 71%) as a light yellowish gum. LRMS (APCI+) m/z 258.1 (M+H).

Step 2: tert-butyl (6-(methylsulfonyl)spiro[3.3]heptan-2-yl)carbamate. To a solution of tert-butyl (6-(methylthio)spiro[3.3]heptan-2-yl)carbamate (183 mg, 0.71 mmol, 1.0 equiv) in CH₂Cl₂ (3 mL) was added mCPBA (367 mg, 2.13 mmol, 3.0 equiv) at 0° C. The reaction was then stirred at 23° C. for 3 h. Upon completion, a mixed solution of NaHCO₃ and Na₂S₂O₃ was added to quench the reaction. The aqueous phase was extracted by CH₂Cl₂ (5 mL×3). The combined organic phase was washed by brine, dried (MgSO₄), filtered, and concentrated to yield the crude tert-butyl (6-(methylsulfonyl)spiro[3.3]heptan-2-yl)carbamate (169 mg, 83%) as a white solid, which was directly used without further purifications. LRMS (APCI+) m/z 290.2 (M+H).

Step 3: 6-(methylsulfonyl)spiro[3.3]heptan-2-amine. To a solution of tert-butyl (6-(methylsulfonyl)spiro[3.3]heptan-2-yl)carbamate (169 mg, 0.584 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added HCl (4 M in 1,4-dioxane, 1.17 mL, 4.67 mmol, 8.0 equiv). The mixture was stirred at 23° C. for 20 h. Upon completion, the volatile was removed in vacuo to yield the crude 6-(methylsulfonyl)spiro[3.3]heptan-2-amine (Intermediate 26.1, 109 mg, 98%) as a light yellowish gum which was directly used without further purifications. LRMS (APCI+) m/z 190.1 (M+H).

Example AA

Synthesis of Intermediate 27.1

Step 1: tert-butyl (6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-yl)carbamate. To a solution of tert-butyl (6-hydroxyspiro[3.3]heptan-2-yl)carbamate (120 mg, 0.53 mmol, 1.0 equiv) in THF (1 mL) was added NaH (44 mg, 60% suspension in mineral oil, 1.11 mmol, 2.1 equiv) at 0° C. The deprotonation was stirred at 23° C. for 1 h. Then potassium iodide (18 mg, 0.11 mmol, 0.2 equiv) and 4-(chloromethyl)pyridine HCl salt (91 mg, 0.55 mmol, 1.05 equiv) was added sequentially. The reaction was stirred at 23° C. for 4 h. Upon completion, half-saturated NH₄Cl solution (5 mL) was added to quench the reaction. The aqueous phase was extracted by CH₂Cl₂ (3 mL×2). The combined organic phase was washed by brine, dried (MgSO₄), filtered, concentrated, and purified by flash column chromatography (silica, CH₂Cl2/MeOH) to yield tert-butyl (6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-yl)carbamate (139 mg, 83% yield) as a colorless gum. LRMS (APCI+) m/z 319.1 (M+H).

Step 2: 6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-amine. To a solution of tert-butyl (6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-yl)carbamate (139 mg, 0.436 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added HCl (4 M in 1,4-dioxane, 0.87 mL, 3.49 mmol, 8.0 equiv). The mixture was stirred at 23° C. for 20 h. Upon completion, the volatile was removed in vacuo to yield the crude 6-(pyridin-4-ylmethoxy)spiro[3.3]heptan-2-amine (Intermediate 27.1, 95 mg, 99%) as a light yellowish gum which was directly used without further purifications. LRMS (APCI+) m/z 219.1 (M+H).

Intermediate 27.2 was prepared in a similar manner as Intermediate 27.1, using the reagents provided in the table below.

Intermediate	Phenol	Structure, Name and Data
27.2	3-(bromomethyl)pyridine
		Synthesis of 6-(pyridin-3-
		ylmethoxy)spiro[3.3]heptan-2-amine. LRMS
		(APCI) m/z 219.1 (M + H).

Example 1

Preparation of 1-(2-(3-(2-chlorophenyl)propanoyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl) urea (Compound 135)

HATU (207 mg, 0.545 mmol, 1.5 equiv) was added to a stirring solution of 3-(2-chlorophenyl)propanoic acid (101 mg, 0.545 mmol, 1.5 equiv), 1-(4-methoxybenzyl)-3-(2-azaspiro[3.3]heptan-6-yl)urea (100 mg, 0.257 mmol, 1 equiv) and NEt₃ (147 μL, 0.770 mmol, 3 equiv) in DMF (1 mL) at rt. After 4 h, the reaction was diluted with MeOH to a total volume of 1.8 mL, filtered through a 0.4 μm syringe filter, and product isolated by reverse phase HPLC (0->70% MeCN/H2O w/0.1% formic acid) as a white solid (42 mg, 26%). LRMS (APCI) m/z 442 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.34 (dd, J=7.3, 2.7 Hz, 1H), 7.29-7.23 (m, 1H), 7.23-7.12 (m, 2H), 7.07 (d, J=7.4 Hz, 2H), 6.87-6.69 (m, 2H), 6.08 (dt, J=14.0, 6.1 Hz, 2H), 4.02 (d, J=5.8 Hz, 2H), 3.95 (s, 1H), 3.84 (d, J=12.9 Hz, 2H), 3.77 (s, 1H), 3.65 (s, 4H), 2.80 (t, J=7.9 Hz, 2H), 2.39-2.27 (m, 2H), 2.23 (q, J=7.7 Hz, 2H), 1.86 (ddt, J=12.8, 9.3, 5.6 Hz, 2H).

Compounds in the following table were prepared in a similar manner as Compound 135, using the intermediates and reagents as listed.

Compound	Carboxylic
No.	acid	Intermediate	Structure, Name and Data
136	1-(tert- butoxycarbo- nyl)piperi- dine-3- carboxylic acid	3.2
			tert-butyl 3-(6-(3-(4-
			methoxybenzyl)ureido)-2-
			azaspiro[3.3]heptane-2-
			carbonyl)piperidine-1-carboxylate.
			LRMS (APCI) m/z 487 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 7.15 (d, J = 7.6
			Hz, 2H), 6.87 (d, J = 7.6 Hz, 2H), 6.26-
			6.07 (m, 2H), 4.19 (q, J = 8.3 Hz, 1H),
			4.14-4.02 (m, 3H), 3.90 (dt, J = 30.0, 9.6
			Hz, 4H), 3.74 (d, J = 9.2 Hz, 3H), 2.78-
			2.65 (m, 2H), 2.48-2.38 (m, 2H), 2.23
			(d, J = 6.4 Hz, 1H), 1.99 (t, J = 9.5 Hz,
			2H), 1.75 (d, J = 11.3 Hz, 1H), 1.60 (t, J =
			16.2 Hz, 2H), 1.40 (d, J = 2.3 Hz, 9H),
			1.14 (t, J = 6.7 Hz, 1H), 1.00 (t, J = 6.9
			Hz, 1H).
137	1,2,3,4- tetrahydro- naphthalene- 1- carboxylic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(1,2,3,4-
			tetrahydronaphthalene-1-carbonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 434 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.16 (d, J = 7.5 Hz,
			2H), 7.09 (d, J = 6.0 Hz, 3H), 6.92 (d, J =
			5.8 Hz, 1H), 6.87 (d, J = 7.4 Hz, 2H), 6.24-
			6.10 (m, 2H), 4.31 (d, J = 8.2 Hz, 1H),
			4.17 (dd, J = 17.3, 8.9 Hz, 1H), 4.11 (d, J =
			4.8 Hz, 2H), 4.03 (d, J = 8.8 Hz, 1H),
			4.00-3.88 (m, 2H), 3.83 (d, J = 12.2 Hz,
			1H), 3.73 (s, 3H), 3.69 (d, J = 6.2 Hz, 1H),
			2.73 (d, J = 19.4 Hz, 2H), 2.48-2.40 (m,
			1H), 2.11-1.85 (m, 4H), 1.77 (q, J =
			11.1, 9.6 Hz, 1H), 1.70-1.54 (m, 1H).
138	6- methylnico- tinic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(6-
			methylnicotinoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 395 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 8.64-8.50 (m, 1H),
			7.87 (t, J = 5.7 Hz, 1H), 7.29 (d, J = 8.0
			Hz, 1H), 7.08 (d, J = 7.7 Hz, 2H), 6.76 (d,
			J = 7.6 Hz, 2H), 4.35 (s, 1H), 4.22 (s, 1H),
			4.11 (s, 3H), 4.00 (s, 1H), 3.94 (dd, J =
			14.8, 8.2 Hz, 1H), 3.66 (s, 3H), 2.50 (d, J =
			10.5 Hz, 5H), 2.01 (t, J = 9.4 Hz, 2H).
139	isonicotinic acid	3.2
			1-(2-isonicotinoyl-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 381 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 8.63 (s, 2H), 7.61 (d, J =
			10.6 Hz, 2H), 7.08 (d, J = 7.7 Hz, 2H),
			6.76 (d, J = 7.8 Hz, 2H), 4.33 (s, 1H), 4.20
			(s, 1H), 4.14 (s, 1H), 4.11 (s, 2H), 4.02 (s,
			1H), 3.95 (dt, J = 16.1, 7.9 Hz, 1H), 3.67
			(s, 3H), 2.62-2.43 (m, 2H), 2.02 (q, J =
			9.4, 8.4 Hz, 2H).
140	2- methylisoni- cotinic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-
			methylisonicotinoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 395 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 8.42 (q, J = 4.3 Hz,
			1H), 7.38 (s, 1H), 7.31 (d, J = 6.7 Hz, 1H),
			7.08 (d, J = 7.7 Hz, 2H), 6.76 (d, J = 7.7
			Hz, 2H), 4.30 (s, 1H), 4.17 (s, 1H), 4.12
			(s, 3H), 4.00 (s, 1H), 3.93 (dd, J = 17.2,
			9.2 Hz, 1H), 3.67 (s, 3H), 2.50 (q, J = 5.0,
			3.5 Hz, 5H), 2.01 (q, J = 8.8, 8.0 Hz, 2H).
141	benzoic acid	3.2
			1-(2-benzoyl-2-azaspiro[3.3]heptan-6-
			yl)-3-(4-methoxybenzyl)urea. LRMS
			(APCI) m/z 380 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 6.88 (s, 2H), 6.73 (dd,
			J = 16.2, 5.6 Hz, 3H), 6.44 (d, J = 7.9 Hz,
			2H), 6.12 (d, J = 7.9 Hz, 2H), 3.57 (d, J =
			50.9 Hz, 3H), 3.44 (s, 3H), 3.27 (d, J =
			33.3 Hz, 2H), 3.01 (s, 2H), 1.83 (d, J =
			11.7 Hz, 4H). 1.35 d, J = 10.7 Hz, 2H).
142	2-methyl- 2- phenylpro- panoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-methyl-2-
			phenylpropanoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 422 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.28 (d, J = 7.7 Hz,
			2H), 7.24-7.12 (m, 3H), 7.04 (d, J = 7.7
			Hz, 2H), 6.77 (d, J = 7.8 Hz, 2H), 6.06 (s,
			1H), 5.95 (dd, J = 29.4, 6.8 Hz, 1H), 3.98
			(s, 2H), 3.76 (s, 2H), 3.64 (s, 5H), 3.14 (s,
			1H), 2.12 (dt, J = 59.7, 9.2 Hz, 2H), 1.71
			(dt, J = 51.5, 9.9 Hz, 2H), 1.31 (s, 6H).
143	1- phenylcyclo- propane- 1- carboxylic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(1-
			phenylcyclopropane-1-carbonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 420 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.36 (d, J = 7.5 Hz,
			2H), 7.30 (d, J = 7.7 Hz, 3H), 7.05 (d, J =
			7.5 Hz, 2H), 6.78 (d, J = 7.5 Hz, 2H), 6.07
			(s, 1H), 6.00 (dd, J = 15.7, 7.8 Hz, 1H),
			5.01 (s, 2H), 4.63 (s, 2H), 4.00 (s, 2H),
			3.89 (s, 1H), 3.86-3.68 (m, 2H), 3.64 (s,
			3H), 3.60 (s, 1H), 3.46 (s, 1H), 2.24 (dt, J =
			38.4, 9.4 Hz, 2H), 1.80 (dt, J = 34.6, 9.7
			Hz, 2H).
144	1-methyl- 6-oxo-1,6- dihydropyri- dine-3- carboxylic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(1-methyl-6-
			oxo-1,6-dihydropyridine-3-carbonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 411 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.06 (s, 1H), 7.56 (d, J =
			9.1 Hz, 1H), 7.08 (d, J = 7.5 Hz, 2H),
			6.79 (d, J = 7.7 Hz, 2H), 6.31 (d, J = 9.5
			Hz, 1H), 6.08 (d, J = 7.9 Hz, 2H), 4.26 (d,
			J = 50.1 Hz, 2H), 4.02 (s, 2H), 3.99-3.77
			(m, 3H), 3.65 (s, 3H), 3.40 (s, 3H), 2.37
			(d, J = 8.5 Hz, 2H), 1.92 (t, J = 9.6 Hz,
			2H).
145	4- methylbenzo- ic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(4-
			methylbenzoyl)-2-azaspiro[3.3]heptan-
			6-yl)urea. LRMS (APCI) m/z 394
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.44 (d, J = 6.6 Hz, 2H), 7.17 (d, J = 7.8
			Hz, 2H), 7.07 (d, J = 8.6 Hz, 2H), 6.79 (d,
			J = 8.6 Hz, 2H), 6.17-6.00 (m, 2H), 4.25
			(s, 1H), 4.13 (s, 1H), 4.02 (d, J = 5.9 Hz,
			2H), 3.99 (s, 1H), 3.87 (s, 2H), 3.65 (s,
			3H), 2.42-2.32 (m, 2H), 2.27 (s, 3H),
			1.93 (d, J = 10.8 Hz, 2H).
146	3- methylbenzo- ic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-
			methylbenzoyl)-2-azaspiro[3.3]heptan-
			6-yl)urea. LRMS (APCI) m/z 394
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.35 (s, 1H), 7.30 (d, J = 5.3 Hz, 1H), 7.28-
			7.20 (m, 2H), 7.07 (d, J = 8.7 Hz, 2H),
			6.79 (d, J = 8.7 Hz, 2H), 6.08 (s, 2H), 4.25
			(s, 1H), 4.12 (s, 1H), 4.02 (d, J = 5.1 Hz,
			2H), 3.99 (s, 1H), 3.87 (s, 2H), 3.65 (s,
			3H), 2.42-2.34 (m, 2H), 2.27 (s, 3H),
			1.99-1.83 (m, 2H).
147	4- (trifluorometh- yl)benzo- ic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(4-
			(trifluoromethyl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 448 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.82 (d, J = 3.9 Hz,
			4H), 7.15 (d, J = 8.7 Hz, 2H), 6.86 (d, J =
			8.6 Hz, 2H), 6.22-6.08 (m, 2H), 4.35 (s,
			1H), 4.22 (s, 1H), 4.16-4.04 (m, 3H),
			4.00 (s, 1H), 3.99-3.85 (m, 1H), 3.72 (s,
			3H), 2.47 (d, J = 9.8 Hz, 2H), 2.00 (q, J =
			10.3 Hz, 2H).
148	2- methylbenzo- ic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-
			methylbenzoyl)-2-azaspiro[3.3]heptan-
			6-yl)urea. LRMS (APCI) m/z 394
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.28-7.21 (m, 1H), 7.21-7.10 (m, 3H),
			7.07 (d, J = 8.6 Hz, 2H), 6.78 (d, J = 8.4
			Hz, 2H), 6.06 (dd, J = 11.5, 7.1 Hz, 2H),
			4.01 (d, J = 5.4 Hz, 2H), 3.98 (s, 1H), 3.95-
			3.76 (m, 3H), 3.70 (s, 1H), 3.65 (s, 3H),
			2.42-2.30 (m, 2H), 2.20 (s, 3H), 1.90
			(dtd, J = 22.8, 8.9, 2.9 Hz, 2H).
153	2-methyl- 2-(p- tolyl)propa- noic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-methyl-2-
			(p-tolyl)propanoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 436 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.12-7.01 (m, 6H),
			6.78-6.68 (m, 2H), 4.07 (s, 2H), 3.85 (s,
			2H), 3.72 (s, 2H), 3.65 (s, 3H), 3.34 (s,
			1H), 2.30 (ddd, J = 10.1, 7.5, 3.0 Hz, 1H),
			2.23 (d, J = 4.5 Hz, 3H), 2.17 (ddd, J =
			12.7, 6.6, 3.0 Hz, 1H), 1.82 (td, J = 8.9,
			3.1 Hz, 1H), 1.70 (td, J = 8.9, 3.0 Hz, 1H),
			1.34 (d, J = 3.3 Hz, 6H).
154	2-methyl- 2-(m- tolyl)propa- noic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-methyl-2-
			(m-tolyl)propanoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 436 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.14 (q, J = 7.8 Hz,
			1H), 7.08-7.02 (m, 2H), 7.02-6.92 (m,
			3H), 6.78-6.69 (m, 2H), 4.07 (s, 2H),
			3.86 (s, 2H), 3.73 (m, 2H), 3.65 (s, 3H),
			3.34 (s, 1H), 2.30 (ddd, J = 10.2, 7.8, 2.8
			Hz, 1H), 2.24 (d, J = 5.0 Hz, 3H), 2.16
			(ddd, J = 10.0, 7.7, 2.7 Hz, 1H), 1.83 (td, J =
			9.0, 2.9 Hz, 1H), 1.70 (td, J = 8.9, 2.8
			Hz, 1H), 1.35 (d, J = 3.5 Hz, 6H).
155	4- methoxyben- zoic acid	3.2
			1-(2-(4-methoxybenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 410 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.51 (t, J = 6.6 Hz, 2H),
			7.08 (d, J = 8.7 Hz, 2H), 6.88 (d, J = 8.4
			Hz, 2H), 6.79-6.72 (m, 2H), 4.33 (s,
			1H), 4.20 (s, 1H), 4.11 (s, 2H), 4.09 (s,
			1H), 3.97 (s, 2H), 3.74 (s, 3H), 3.66 (s,
			3H), 2.50 (ddd, J = 10.1, 7.7, 2.8 Hz, 2H),
			2.06-1.91 (m, 2H).
156	4- cyanobenzo- ic acid	3.2
			1-(2-(4-cyanobenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			405 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.80-7.64 (m, 4H), 7.08
			(d, J = 8.6 Hz, 2H), 6.76 (d, J = 8.6 Hz,
			2H), 4.30 (s, 1H), 4.17 (s, 1H), 4.13 (s,
			1H), 4.11 (s, 2H), 4.01 (s, 1H), 3.94 (dt, J =
			17.0, 8.0 Hz, 1H), 3.67 (s, 3H), 2.57-
			2.41 (m, 2H), 2.01 (q, J = 9.7 Hz, 2H).
157	4-(2- hydroxypro- pan-2- yl)benzoic acid	3.2
			1-(2-(4-(2-hydroxypropan-2-
			yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-
			3-(4-methoxybenzyl)urea. LRMS
			(APCI) m/z 438 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.55-7.43 (m, 4H),
			7.08 (d, J = 8.7 Hz, 2H), 6.76 (d, J = 8.6
			Hz, 2H), 4.32 (s, 1H), 4.19 (s, 1H), 4.11
			(d, J = 2.7 Hz, 3H), 3.99 (s, 1H), 3.94 (dd,
			J = 16.5, 8.2 Hz, 1H), 3.67 (s, 3H), 2.57-
			2.41 (m, 2H), 2.01 (td, J = 8.8, 3.9 Hz,
			2H), 1.44 (s, 6H).
158	4- chlorobenzo- ic acid	3.2
			1-(2-(4-chlorobenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 414 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.53 (t, J = 7.6 Hz, 2H),
			7.37 (dd, J = 8.4, 3.6 Hz, 2H), 7.12-7.02
			(m, 2H), 6.80-6.70 (m, 2H), 4.31 (s,
			1H), 4.17 (s, 1H), 4.11 (d, J = 2.6 Hz, 3H),
			3.98 (s, 1H), 3.97-3.86 (m, 1H), 3.66 (s,
			3H), 2.56-2.42 (m, 2H), 2.00 (td, J =
			12.0, 10.4, 4.0 Hz, 2H).
172	3- ethylbenzoic acid	3.2
			1-(2-(3-ethylbenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			408 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ δ 7.48 (d, J = 4.9 Hz, 1H),
			7.43 (dd, J = 6.6, 4.2 Hz, 1H), 7.38 (d, J =
			4.1 Hz, 2H), 7.20 (d, J = 8.6 Hz, 2H), 6.87
			(d, J = 8.5 Hz, 2H), 4.41 (s, 1H), 4.27 (s,
			1H), 4.22 (d, J = 2.9 Hz, 3H), 4.07 (d, J =
			25.2 Hz, 2H), 3.78 (s, 3H), 2.71 (qd, J =
			7.6, 2.8 Hz, 2H), 2.62 (ddt, J = 12.2, 7.4,
			3.4 Hz, 2H), 2.12 (ddt, J = 13.1, 8.6, 3.5
			Hz, 2H), 1.27 (td, J = 7.6, 2.4 Hz, 3H).
173	3- isopropylben- zoic acid	3.2
			1-(2-(3-isopropylbenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 422 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.39 (d, J = 4.6 Hz, 1H),
			7.36-7.22 (m, 3H), 7.08 (d, J = 8.6 Hz,
			2H), 6.75 (d, J = 8.5 Hz, 2H), 4.29 (s, 1H),
			4.16 (s, 1H), 4.11 (s, 3H), 3.98 (s, 1H),
			3.92 (dt, J = 16.3, 9.2 Hz, 1H), 3.66 (s,
			3H), 2.86 (pd, J = 6.9, 3.1 Hz, 1H), 2.50
			(ddt, J = 10.2, 6.9, 3.0 Hz, 2H), 1.99 (tt, J =
			8.3, 3.6 Hz, 2H), 1.23-1.10 (m, 6H).
174	3-(tert- butyl)benzo- ic acid	3.2
			1-(2-(3-(tert-butyl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 436 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.57 (dd, J = 4.5, 2.4 Hz,
			1H), 7.47 (ddd, J = 7.3, 3.8, 2.0 Hz, 1H),
			7.30 (ddt, J = 10.7, 7.7, 4.5 Hz, 2H), 7.08
			(d, J = 8.6 Hz, 2H), 6.75 (d, J = 8.4 Hz,
			2H), 4.29 (s, 1H), 4.16 (s, 1H), 4.11 (s,
			3H), 3.99 (s, 1H), 3.93 (dd, J = 18.1, 8.8
			Hz, 1H), 3.66 (s, 3H), 2.50 (ddt, J = 10.4,
			7.3, 3.1 Hz, 2H), 2.09-1.90 (m, 2H),
			1.25 (d, J = 2.5 Hz, 9H).
175	3-(2- hydroxypro- pan-2- yl)benzoic acid	3.2
			1-(2-(3-(2-hydroxypropan-2-
			yl)benzoyl)-2-azaspiro[3.3]heptan-6-yl)-
			3-(4-methoxybenzyl)urea. LRMS
			(APCI) m/z 438 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.66 (d, J = 5.5 Hz,
			1H), 7.53 (d, J = 7.8 Hz, 1H), 7.37 (t, J =
			7.0 Hz, 1H), 7.31 (td, J = 7.7, 4.0 Hz, 1H),
			7.08 (d, J = 8.6 Hz, 2H), 6.75 (d, J = 8.5
			Hz, 2H), 4.30 (s, 1H), 4.17 (s, 1H), 4.11
			(s, 3H), 3.99 (s, 1H), 3.93 (dd, J = 18.1,
			8.2 Hz, 1H), 3.66 (s, 3H), 2.49 (d, J = 12.8
			Hz, 2H), 2.00 (q, J = 13.5, 10.4 Hz, 2H),
			1.44 (d, J = 1.2 Hz, 6H).
176	3- methoxy- benzoic acid	3.2
			1-(2-(3-methoxybenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzoyl)urea. LRMS (APCI) m/z
			410 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.26 (td, J = 7.9, 4.2 Hz,
			1H), 7.12-7.03 (m, 4H), 7.01-6.93 (m,
			1H), 6.75 (d, J = 8.6 Hz, 2H), 4.29 (s, 1H),
			4.16 (s, 1H), 4.10 (d, J = 3.9 Hz, 3H), 3.98
			(s, 1H), 3.97-3.87 (m, 1H), 3.73 (d, J =
			2.5 Hz, 3H), 3.66 (s, 3H), 2.55-2.43 (m,
			2H), 2.00 (q, J = 9.5, 6.7 Hz, 2H).
177	3- hydroxyben- zoic acid	3.2
			1-(2-(3-hydroxybenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			396 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.16 (td, J = 7.8, 4.2 Hz,
			1H), 7.11-7.05 (m, 2H), 6.94 (dd, J =
			14.5, 6.0 Hz, 2H), 6.81 (d, J = 8.2 Hz,
			1H), 6.78-6.70 (m, 2H), 4.28 (s, 1H),
			4.15 (s, 1H), 4.11 (s, 2H), 4.09 (s, 1H),
			3.99-3.88 (m, 2H), 3.66 (s, 3H), 2.56-
			2.41 (m, 2H), 2.06-1.90 (m, 2H).
178	3- (dimethyla- mino)benzo- ic acid	3.2
			1-(2-(3-(dimethylamino)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			423 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.16 (td, J = 8.0, 4.5 Hz,
			1H), 7.11-7.05 (m, 2H), 6.85 (d, J = 3.9
			Hz, 1H), 6.82-6.71 (m, 4H), 4.28 (s,
			1H), 4.15 (s, 1H), 4.11 (s, 2H), 4.09 (s,
			1H), 3.94 (d, J = 21.2 Hz, 2H), 3.66 (s,
			3H), 2.86 (d, J = 2.6 Hz, 6H), 2.49 (ddt, J =
			10.1, 7.5, 3.6 Hz, 2H), 2.00 (td, J = 8.8,
			3.6 Hz, 2H).
179	3- (pyrrolidin- 1- yl)benzoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-
			(pyrrolidin-1-yl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 449 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.12 (ddt, J = 10.1,
			4.5, 2.3 Hz, 2H), 7.09-7.03 (m, 2H),
			6.75 (d, J = 8.3 Hz, 2H), 6.69 (t, J = 7.7
			Hz, 1H), 6.65 (p, J = 1.9 Hz, 1H), 6.59 (dt,
			J = 8.3, 3.0 Hz, 1H), 4.27 (s, 1H), 4.14 (s,
			1H), 4.11 (s, 2H), 4.08 (s, 1H), 3.94 (d, J =
			19.3 Hz, 2H), 3.66 (s, 3H), 3.19 (d, J =
			3.7 Hz, 4H), 2.56-2.42 (m, 2H), 2.03-
			1.85 (m, 5H).
180	3- methylsunfo- nylbenzoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-
			(methylsulfonyl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 458 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 8.14-8.07 (m, 1H),
			8.00 (d, J = 7.9 Hz, 1H), 7.88 (t, J = 6.5
			Hz, 1H), 7.64 (td, J = 7.8, 3.4 Hz, 1H),
			7.08 (d, J = 8.6 Hz, 2H), 6.76 (d, J = 8.7
			Hz, 2H), 4.35 (s, 1H), 4.22 (s, 1H), 4.15
			(s, 1H), 4.12 (s, 2H), 4.03 (s, 1H), 3.94
			(dq, J = 16.3, 8.0 Hz, 1H), 3.67 (s, 3H),
			3.06 (d, J = 2.4 Hz, 3H), 2.52 (ddd, J =
			12.6, 6.3, 2.7 Hz, 2H), 2.02 (qd, J = 8.1,
			6.4, 3.3 Hz, 2H).
181	3- (methoxycar- bonyl)ben- zoic acid	3.2
			methyl 3-(6-(3-(4-
			methoxybenzyl)ureido)-2-
			azaspiro[3.3]heptane-2-
			carbonyl)benzoate. LRMS (APCI) m/z
			438 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 8.16 (d, J = 5.5 Hz, 1H),
			8.05 (d, J = 7.9 Hz, 1H), 7.77 (t, J = 6.4
			Hz, 1H), 7.49 (td, J = 7.8, 3.4 Hz, 1H),
			7.08 (d, J = 8.6 Hz, 2H), 6.75 (d, J = 8.5
			Hz, 2H), 4.33 (s, 1H), 4.20 (s, 1H), 4.13
			(s, 1H), 4.11 (s, 2H), 4.01 (s, 1H), 3.94
			(dt, J = 16.8, 8.1 Hz, 1H), 3.84 (d, J = 1.4
			Hz, 3H), 3.66 (s, 3H), 2.51 (dq, J = 10.1,
			3.1 Hz, 2H), 2.01 (td, J = 8.8, 4.2 Hz, 2H).
188	3-(2- oxypyrrolidin- 1- yl)benzoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-(2-
			oxopyrrolidin-1-yl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 463 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.89 (s, 1H), 7.61 (t,
			J = 8.9 Hz, 1H), 7.43-7.30 (m, 2H), 7.08
			(d, J = 8.6 Hz, 2H), 6.76 (d, J = 8.4 Hz,
			2H), 4.33 (s, 1H), 4.21 (s, 1H), 4.12 (s,
			3H), 3.96 (d, J = 27.1 Hz, 2H), 3.86 (td, J =
			7.1, 2.7 Hz, 2H), 3.67 (s, 3H), 2.51 (q, J =
			6.8, 5.6 Hz 4H), 2.10 (p, J = 7.7 Hz,
			2H), 2.05-1.95 (m, 2H).
189	3-(1H- pyrrol-1- yl)benzoic acid	3.2
			1-(2-(3-(1H-pyrrol-1-yl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 445 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.73 (p, J = 1.9 Hz, 1H),
			7.65 (d, J = 8.2 Hz, 1H), 7.62-7.52 (m,
			1H), 7.50 (dd, J = 4.5, 2.7 Hz, 1H), 7.25
			(p, J = 1.6 Hz, 2H), 7.20 (d, J = 8.6 Hz,
			2H), 6.87 (d, J = 8.2 Hz, 2H), 6.33 (q, J =
			2.1 Hz, 2H), 4.46 (s, 1H), 4.33 (s, 1H),
			4.25 (s, 1H), 4.23 (s, 2H), 4.17-4.00 (m,
			2H), 3.78 (s, 3H), 2.63 (dd, J = 11.7, 7.8
			Hz, 2H), 2.13 (t, J = 9.2 Hz, 2H).
190	3- (piperidin- 1- yl)benzoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-(piperidin-
			1-yl)benzoyl)-2-azaspiro[3.3]heptan-6-
			yl)urea. LRMS (APCI) m/z 463 (M + H).
			1H NMR (400 MHz, Methanol-d4) δ 7.26-
			7.14 (m, 1H), 7.09 (dq, J = 9.3, 3.1 Hz,
			3H), 7.01 (d, J = 8.3 Hz, 1H), 6.91 (t, J =
			7.5 Hz, 1H), 6.81-6.71 (m, 2H), 4.28 (s,
			1H), 4.19-4.06 (m, 4H), 3.96 (d, J = 12.9
			Hz, 2H), 3.79 (s, 1H), 3.67 (s, 3H), 3.10
			(dq, J = 8.7, 3.7 Hz, 4H), 2.56-2.44 (m,
			2H), 2.05-1.94 (m, 1H), 1.63 (q, J = 4.4,
			3.9 Hz, 4H), 1.52 (d, J = 5.5 Hz, 2H).
191	3- morpholino benzoic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(3-
			morpholinobenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 465 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.28-7.20 (m, 1H),
			7.14-7.05 (m, 3H), 7.04-6.93 (m, 2H),
			6.76 (d, J = 8.5 Hz, 2H), 4.29 (s, 1H), 4.16
			(s, 1H), 4.12 (s, 2H), 4.10 (s, 1H), 3.95 (d,
			J = 22.4 Hz, 2H), 3.75 (dq, J = 5.3, 2.8
			Hz, 4H), 3.67 (s, 3H), 3.09 (dq, J = 5.3,
			2.5 Hz, 4H), 2.55-2.43 (m, 2H), 2.00 (dt,
			J = 11.2, 6.5 Hz, 2H).
38	2-(2- fluorophenyl) acetic acid	3.2
			1-(2-(2-(2-fluorophenyl)acetyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			412 (M + H). 1H NMR (400 MHz, DMSO-
			d6) δ 7.28 (t, J = 7.1 Hz, 2H), 7.15 (dd, J =
			7.7, 4.6 Hz, 4H), 6.87 (d, J = 8.3 Hz, 2H),
			6.25-6.09 (m, 2H), 4.22 (s, 1H), 4.11 (d,
			J = 5.6 Hz, 3H), 3.96 (p, J = 8.0 Hz, 1H),
			3.89 (s, 1H), 3.76 (s, 1H), 3.73 (d, J = 0.8
			Hz, 3H), 3.44 (d, J = 5.9 Hz, 2H), 2.48-
			2.36 (m, 2H), 2.00 (tt, J = 9.0, 3.6 Hz,
			2H).
39	2-(2- chlorophenyl) acetic acid	3.2
			1-(2-(2-(2-chlorophenyl)acetyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI)
			m/z 428 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.47-7.38 (m, 1H), 7.37-
			7.31 (m, 1H), 7.31-7.21 (m, 2H), 7.16
			(d, J = 8.4 Hz, 2H), 6.94-6.77 (m, 2H),
			6.27-6.06 (m, 2H), 4.23 (s, 1H), 4.17-
			4.03 (m, 4H), 3.97 (p, J = 8.0 Hz, 1H),
			3.90 (s, 1H), 3.79 (s, 1H), 3.53 (d, J = 5.0
			Hz, 2H), 3.18 (d, J = 5.0 Hz, 2H), 2.49-
			2.36 (m, 1H), 2.01 (td, J = 8.9, 4.4 Hz,
			2H).
40	2-(2- methoxyphe- nyl)acetic aicd	3.2
			1-(4-methoxybenzyl)-3-(2-(2-(2-
			methoxyphenyl)acetyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 424 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.29-7.17 (m, 1H),
			7.14 (t, J = 8.6 Hz, 3H), 6.95 (d, J = 8.2
			Hz, 1H), 6.88 (dd, J = 8.0, 5.9 Hz, 3H),
			6.27-6.05 (m, 2H), 4.10 (d,
			J = 5.9 Hz, 2H), 4.06 (s, 1H), 3.95 (h, J =
			7.1 Hz, 1H), 3.87 (s, 1H), 3.77 (s, 1H),
			3.76 (s, 3H), 3.73 (s, 3H), 3.31 (d, J = 4.5
			Hz, 2H), 2.44 (ddt, J = 12.1, 7.7, 3.7 Hz,
			2H), 2.00 (td, J = 8.8, 4.4 Hz, 2H).
41	2-(2- (trifluorometh- yl)phenyl) acetic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-(2-
			(trifluoromethyl)phenyl)acetyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 462 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.68 (d, J = 7.8 Hz,
			1H), 7.62 (t, J = 7.6 Hz, 1H), 7.45 (dd, J =
			18.3, 7.8 Hz, 2H), 7.16 (d, J = 8.5 Hz,
			2H), 6.93-6.77 (m, 2H), 6.24-6.05 (m,
			2H), 4.21 (s, 1H), 4.14-4.02 (m, 3H),
			3.96 (q, J = 8.0 Hz, 1H), 3.90 (s, 1H), 3.79
			(s, 1H), 3.73 (s, 3H), 3.59 (d, J = 6.3 Hz,
			2H), 2.45 (s, 2H), 2.01 (tt, J = 8.4, 3.7 Hz,
			2H).
42	2-(o- tolyl)acetic acid	3.2
			1-(4-methoxybenzyl)-3-(2-(2-(o-
			tolyl)acetyl)-2-azaspiro[3.3]heptan-6-
			yl)urea. LRMS (APCI) m/z 408 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.19-
			7.03 (m, 6H), 6.87 (d, J = 8.2 Hz, 2H),
			6.25-6.07 (m, 2H), 4.19 (s, 1H), 4.10 (d,
			J = 5.7 Hz, 2H), 4.06 (s, 1H), 3.96 (q, J =
			8.0 Hz, 1H), 3.90 (s, 1H), 3.78 (s, 1H),
			3.73 (s, 3H), 3.40 (d, J = 4.6 Hz, 2H), 2.47-
			2.36 (m, 2H), 2.21 (t, J = 1.5 Hz, 3H),
			1.99 (td, J = 8.9, 2.9 Hz, 2H).
222	3- (pyrrolidin- 1- yl)benzoic acid	3.3
			4-((3-(2-(3-(pyrrolidin-1-yl)benzoyl)-2-
			azaspiro[3.3]heptan-6-
			yl)ureido)methyl)benzamide. LRMS
			(APCI) m/z 462 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.73 (d, J = 8.0 Hz,
			2H), 7.26 (d, J = 8.0 Hz, 2H), 7.13 (td, J =
			7.9, 3.5 Hz, 1H), 6.70 (t, J = 7.2 Hz, 1H),
			6.66 (s, 1H), 6.60 (d, J = 8.3 Hz, 1H), 4.49
			(s, 2H), 4.29 (s, 1H), 4.26 (s, 2H), 4.16 (s,
			1H), 4.10 (s, 1H), 3.95 (d, J = 20.2 Hz,
			3H), 2.51 (s, 3H), 2.09-1.98 (m, 2H),
			1.98-1.86 (m, 4H).
223	5- (pyrrolidin- 1- yl)nicotinic acid	3.3
			4-((3-(2-(5-(pyrrolidin-1-yl)nicotinoyl)-
			2-azaspiro[3.3]heptan-6-
			yl)ureido)methyl)benzamide. LRMS
			(APCI) m/z 463 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.87 (s, 2H), 7.72
			(d, J = 8.0 Hz, 2H), 7.26 (d, J = 8.1 Hz,
			2H), 7.03 (s, 1H), 4.48 (s, 1H), 4.32 (s,
			1H), 4.25 (s, 2H), 4.20 (s, 1H), 4.12 (s,
			1H), 4.07-3.87 (m, 3H), 3.25 (s, 2H),
			2.57 -2.42 (m, 2H), 2.08-1.93 (m, 6H).
224	3- chlorobenzo- ic acid	3.3
			4-((3-(2-(4-chlorobenzoyl)-2-
			azaspiro[3.3]heptan-6-
			yl)ureido)methyl)benzamide. LRMS
			(APCI) m/z 427 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.72 (d, J = 8.0 Hz,
			2H), 7.53 (dd, J = 8.1, 5.9 Hz, 2H), 7.37
			(dd, J = 8.5, 2.5 Hz, 2H), 7.26 (d, J = 8.1
			Hz, 2H), 4.31 (s, 1H), 4.25 (s, 2H), 4.18
			(s, 1H), 4.11 (s, 1H), 4.03-3.87 (m, 2H),
			2.50 (ddd, J = 10.6, 7.2, 3.5 Hz, 2H), 2.02
			(td, J = 8.9, 4.2 Hz, 2H).
225	6- methylnico- tinic acid	3.3
			4-((3-(2-(6-methylnicotinoyl)-2-
			azaspiro[3.3]heptan-6-
			yl)ureido)methyl)benzamide. LRMS
			(APCI) m/z 408 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 8.72 (d, J = 6.6 Hz,
			1H), 8.19-8.00 (m, 2H), 7.84 (d, J = 8.2
			Hz, 2H), 7.47 (dd, J = 8.3, 3.7 Hz, 1H),
			7.37 (d, J = 8.2 Hz, 2H), 4.47 (s, 1H), 4.37
			(s, 2H), 4.34 (s, 1H), 4.24 (s, 1H), 4.13 (s,
			1H), 4.06 (dq, J = 15.5, 7.7 Hz, 1H), 2.94
			(d, J = 4.5 Hz, 1H), 2.62 (m, 3H), 2.15 (t,
			J = 9.4 Hz, 2H).
226	2- methylisoni- cotinic acid	3.3
			4-((3-(2-(2-methylisonicotinoyl)-2-
			azaspiro[3.3]heptan-6-
			yl)ureido)methyl)benzamide. LRMS
			(APCI) m/z 408 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 8.60 (t, J = 6.6 Hz,
			1H), 7.79 (d, J = 12.3 Hz, 1H), 7.72 (d, J =
			8.2 Hz, 3H), 7.26 (d, J = 8.0 Hz, 2H),
			4.33 (s, 1H), 4.25 (s, 2H), 4.20 (s, 1H),
			4.16 (s, 1H), 4.04 (s, 1H), 3.95 (dt, J =
			15.8, 7.9 Hz, 1H), 2.66 (d, J = 6.0 Hz,
			3H), 2.51 (t, J = 8.8 Hz, 2H), 2.05 (dd, J =
			11.4, 7.3 Hz, 2H).
219	3-(1H- pyrrol-1- yl)benzoic acid	3.1
			1-(2-(3-(1H-pyrrol-1-yl)benzoyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			chlorobenzyl)urea. LRMS (APCI) m/z
			449 (M + H). 1H NMR (400 MHz, DMSO-
			d6) δ 7.75-7.69 (m, 2H), 7.57-7.49 (m,
			1H), 7.48-7.41 (m, 3H), 7.36 (d, J = 8.4
			Hz, 2H), 7.24 (d, J = 8.4 Hz, 2H), 6.33-
			6.27 (m, 3H), 6.24 (dd, J = 8.0, 3.7 Hz,
			1H), 4.39 (s, 1H), 4.26 (s, 1H), 4.16 (d, J =
			6.0 Hz, 2H), 4.10 (s, 1H), 3.96 (d, J =
			21.5 Hz, 2H), 2.46 (s, 2H), 2.02 (d, J =
			10.3 Hz, 2H).
220	3- isopropylben- zoic acid	3.1
			1-(4-chlorobenzyl)-3-(2-(3-
			isopropylbenzoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 426 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.47 (s, 1H), 7.43-
			7.32 (m, 5H), 7.27-7.20 (m, 2H), 6.31 (t,
			J = 6.1 Hz, 1H), 6.24 (t, J = 7.9 Hz, 1H),
			4.33 (s, 1H), 4.21 (s, 1H), 4.16 (d, J = 6.0
			Hz, 2H), 4.07 (s, 1H), 3.99-3.88 (m,
			3H), 2.94 (hept, J = 6.9 Hz, 1H), 2.47 (s,
			1H), 2.00 (dt, J = 9.9, 5.4 Hz, 2H), 1.22
			(d, J = 6.9 Hz, 6H).
221	2-methyl- 2- phenylpropa- noic acid	3.1
			1-(4-chlorobenzyl)-3-(2-(2-methyl-2-
			phenylpropanoyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 426 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.41-7.29 (m, 4H),
			7.29-7.16 (m, 5H), 6.27 (t, J = 6.1 Hz,
			1H), 6.12 (dd, J = 30.8, 7.9 Hz, 1H), 4.12
			(d, J = 5.9 Hz, 2H), 3.83 (s, 2H), 3.69 (d, J =
			26.6 Hz, 2H), 3.21 (s, 1H), 2.27 (s, 1H),
			2.10 (d, J = 17.8 Hz, 1H), 1.86 (t, J = 10.1
			Hz, 1H), 1.75 (d, J = 10.4 Hz, 1H), 1.38
			(s, 6H).
114	benzoic acid	3.1
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)benzamide. LRMS (APCI) m/z 398
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			8.54 (d, J = 7.5 Hz, 1H), 7.87-7.79 (m,
			2H), 7.55-7.48 (m, 1H), 7.45 (dd, J =
			8.2, 6.5 Hz, 2H), 7.40-7.32 (m, 2H),
			7.28-7.22 (m, 2H), 6.28 (t, J = 6.1 Hz,
			1H), 6.22 (d, J = 8.1 Hz, 1H), 4.31 (q, J =
			8.0 Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H), 3.97
			(h, J = 8.3 Hz, 1H), 2.37 (qd, J = 10.2, 9.3,
			6.4 Hz, 2H), 2.25-2.15 (m, 2H), 2.15-
			2.03 (m, 2H), 1.84 (ddd, J = 17.2, 10.5,
			8.4 Hz, 2H).
115	phenylacetic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-phenylacetamide. LRMS (APCI)
			m/z 412 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.24 (d, J = 7.5 Hz, 1H),
			7.36 (d, J = 8.4 Hz, 2H), 7.32-7.19 (m,
			7H), 6.27 (t, J = 6.1 Hz, 1H), 6.19 (d, J =
			8.1 Hz, 1H), 4.15 (d, J = 6.0 Hz, 2H), 4.03
			(q, J = 8.0 Hz, 1H), 3.93 (q, J = 8.2 Hz,
			1H), 2.38-2.26 (m, 3H), 2.15 (dq, J =
			12.9, 7.4 Hz, 3H), 1.95-1.70 (m, 4H).
184	nicotinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)nicotinamide. LRMS (APCI) m/z
			400 (M + H). 1H NMR (400 MHz, DMSO-
			d6) δ 8.98 (d, J = 2.2 Hz, 1H), 8.75 (d, J =
			7.3 Hz, 1H), 8.69 (dd, J = 4.8, 1.7 Hz,
			1H), 8.21-8.13 (m, 1H), 7.50 (dd, J =
			8.0, 4.8 Hz, 1H), 7.41-7.32 (m, 2H),
			7.25 (d, J = 8.3 Hz, 2H), 6.27 (d, J = 5.8
			Hz, 1H), 6.21 (d, J = 8.0 Hz, 1H), 4.31 (q,
			J = 8.0 Hz, 1H), 4.17 (d, J = 5.7 Hz, 2H),
			3.97 (q, J = 7.9 Hz, 1H), 2.45-2.35 (m,
			2H), 2.30-2.16 (m, 2H), 2.16-2.02 (m,
			2H), 1.93-1.77 (m, 2H).
185	isonicotinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)isonicotinamide. LRMS (APCI) m/z
			399 (M + H). 1H NMR (400 MHz, DMSO-
			d6) δ 8.86 (d, J = 7.3 Hz, 1H), 8.77-8.68
			(m, 2H), 7.81-7.69 (m, 2H), 7.45-7.31
			(m, 2H), 7.25 (d, J = 8.3 Hz, 2H), 6.28 (s,
			1H), 6.21 (d, J = 8.1 Hz, 1H), 4.31 (p, J =
			8.0 Hz, 1H), 4.16 (d, J = 5.5 Hz, 2H), 3.97
			(q, J = 7.8 Hz, 1H), 2.39 (ddt, J = 11.1,
			7.8, 4.1 Hz, 2H), 2.27-2.16 (m, 2H),
			2.16-2.02 (m, 2H), 1.84 (ddd, J = 16.4,
			10.4, 8.4 Hz, 2H).
186	2- methylisoni- cotinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-methylisonicotinamide. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.99 (d, J = 7.3 Hz,
			1H), 8.72 (d, J = 5.6 Hz, 1H), 7.89 (s, 1H),
			7.80 (s, 1H), 7.42-7.31 (m, 2H), 7.25 (d,
			J = 8.4 Hz, 2H), 6.26 (d, J = 28.7 Hz, 2H),
			4.30 (q, J = 8.0 Hz, 1H), 4.17 (s, 2H), 3.97
			(s, 1H), 2.64 (s, 3H), 2.40 (dq, J = 12.0,
			6.4 Hz, 2H), 2.22 (ddt, J = 17.4, 12.7, 6.4
			Hz, 2H), 2.16-2.01 (m, 2H), 1.92-1.69
			(m, 2H).
192	6- methylnico- tinic acid	3.4
			c. LRMS (APCI) m/z 413 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.86 (d, J =
			2.3 Hz, 1H), 8.65 (d, J = 7.4 Hz, 1H), 8.06
			(dd, J = 8.1, 2.4 Hz, 1H), 7.41-7.30 (m,
			3H), 7.30-7.17 (m, 2H), 6.28 (t, J = 6.0
			Hz, 1H), 6.21 (d, J = 8.0 Hz, 1H), 4.30 (q,
			J = 8.0 Hz, 1H), 4.16 (d, J = 6.1 Hz, 2H),
			3.97 (q, J = 8.1 Hz, 1H), 3.32 (s, 3H), 2.44-
			2.32 (m, 2H), 2.26-2.16 (m, 2H), 2.08
			(ddd, J = 17.1, 12.4, 9.2 Hz, 2H), 1.93-
			1.76 (m, 2H).
193	2- methylbenzo- ic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-methylbenzamide. LRMS
			(APCI) m/z 412 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.40 (d, J = 7.5 Hz,
			1H), 7.41-7.33 (m, 2H), 7.34-7.15 (m,
			6H), 6.27 (t, J = 6.1 Hz, 1H), 6.20 (d, J =
			8.1 Hz, 1H), 4.24 (q, J = 8.0 Hz, 1H), 4.16
			(d, J = 6.0 Hz, 2H), 3.95 (q, J = 8.0 Hz,
			1H), 2.37 (dt, J = 12.0, 6.3 Hz, 2H), 2.30
			(s, 3H), 2.25-2.12 (m, 2H), 2.09-1.95
			(m, 2H), 1.82 (dt, J = 19.8, 10.0 Hz, 2H).
194	3- methoxyben- zoic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-3-methoxybenzamide. LRMS
			(APCI) m/z 428 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.52 (d, J = 7.5 Hz,
			1H), 7.48-7.31 (m, 5H), 7.25 (d, J = 8.1
			Hz, 2H), 7.07 (dd, J = 7.9, 2.6 Hz, 1H),
			6.27 (t, J = 6.1 Hz, 1H), 6.20 (d, J = 8.1
			Hz, 1H), 4.30 (q, J = 8.1 Hz, 1H), 4.16 (d,
			J = 5.9 Hz, 2H), 3.97 (q, J = 8.0 Hz, 1H),
			3.80 (s, 3H), 2.43-2.27 (m, 2H), 2.21 (dt,
			J = 11.8, 5.6 Hz, 2H), 2.09 (dt, J = 19.4,
			10.0 Hz, 2H), 1.84 (dt, J = 18.7, 10.0 Hz,
			2H).
195	3- (methylsulfo- nyl)benzo- ic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-3-(methylsulfonyl)benzamide.
			LRMS (APCI) m/z 476 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.86 (d, J = 7.4
			Hz, 1H), 8.37 (s, 1H), 8.17 (d, J = 7.8 Hz,
			1H), 8.07 (d, J = 7.8 Hz, 1H), 7.75 (t, J =
			7.8 Hz, 1H), 7.41-7.31 (m, 2H), 7.25 (d,
			J = 8.1 Hz, 2H), 6.28 (t, J = 6.1 Hz, 1H),
			6.21 (d, J = 8.0 Hz, 1H), 4.33 (q, J = 8.0
			Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H), 3.97 (q,
			J = 8.0 Hz, 1H), 3.26 (s, 3H), 2.45-2.35
			(m, 2H), 2.29-2.16 (m, 2H), 2.17-2.03
			(m, 2H), 1.85 (dt, J = 17.2, 9.9 Hz, 2H).
200	3- hydroxyben- zoic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-3-hydroxybenzamide. LRMS
			(APCI) m/z 414 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 9.59 (s, 1H), 8.44 (d, J =
			7.5 Hz, 1H), 7.43-7.32 (m, 2H), 7.29-
			7.18 (m, 5H), 6.88 (dt, J = 6.8, 2.3 Hz,
			1H), 6.27 (t, J = 6.3 Hz, 1H), 6.20 (d, J =
			8.0 Hz, 1H), 4.27 (q, J = 8.0 Hz, 1H), 4.16
			(d, J = 5.9 Hz, 2H), 3.96 (q, J = 8.0 Hz,
			1H), 2.36 (ddd, J = 12.8, 10.2, 6.1 Hz,
			2H), 2.24-2.13 (m, 2H), 2.07 (ddd, J =
			17.0, 11.1, 9.1 Hz, 2H), 1.83 (ddd, J =
			16.7, 10.9, 8.9 Hz, 2H).
203	2- methylnico- tinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-methylnicotinamide. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.60 (d, J = 7.3 Hz,
			1H), 8.50 (dd, J = 4.9, 1.7 Hz, 1H), 7.70
			(d, J = 7.6 Hz, 1H), 7.41-7.33 (m, 2H),
			7.33-7.20 (m, 3H), 6.27 (t, J = 6.1 Hz,
			1H), 6.20 (d, J = 8.1 Hz, 1H), 4.25 (q, J =
			7.9 Hz, 1H), 4.16 (d, J = 5.8 Hz, 2H), 3.96
			(q, J = 7.9 Hz, 1H), 2.50 (s, 3H), 2.44-
			2.31 (m, 2H), 2.20 (ddd, J = 19.4, 14.0,
			8.7 Hz, 2H), 2.10-1.93 (m, 2H), 1.92-
			1.75 (m, 2H).
204	3- methylisoni- cotinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-3-methylisonicotinamide. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.66 (d, J = 7.4 Hz,
			1H), 8.50 (s, 1H), 8.47 (d, J = 5.0 Hz, 1H),
			7.40-7.34 (m, 2H), 7.29 (d, J = 5.0 Hz,
			1H), 7.25 (d, J = 8.3 Hz, 2H), 6.27 (t, J =
			6.0 Hz, 1H), 6.20 (d, J = 8.0 Hz, 1H), 4.24
			(q, J = 7.9 Hz, 1H), 4.16 (d, J = 5.8 Hz,
			2H), 3.96 (q, J = 8.0 Hz, 1H), 2.38 (d, J =
			8.8 Hz, 2H), 2.29 (s, 3H), 2.26-2.12 (m,
			2H), 2.09-1.94 (m, 2H), 1.83 (dt, J =
			19.1, 9.9 Hz, 2H).
205	4- methylnico- tinic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-4-methylnicotinamide. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.66 (d, J = 7.3 Hz,
			1H), 8.48 (d, J = 5.5 Hz, 2H), 7.37 (d, J =
			8.4 Hz, 2H), 7.32 (d, J = 5.1 Hz, 1H), 7.25
			(d, J = 8.4 Hz, 2H), 6.27 (t, J = 6.0 Hz,
			1H), 6.20 (d, J = 8.0 Hz, 1H), 4.25 (q, J =
			7.9 Hz, 1H), 4.16 (d, J = 5.9 Hz, 2H), 3.96
			(q, J = 8.1 Hz, 1H), 2.34 (s, 5H), 2.31-
			2.09 (m, 2H), 2.09-1.92 (m, 2H), 1.83
			(ddd, J = 19.1, 10.4, 8.4 Hz, 2H).
208	2- hydroxyben- zoic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-hydroxybenzamide. LRMS
			(APCI) m/z 414 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 12.67 (d, J = 2.7 Hz,
			1H), 8.86 (d, J = 7.3 Hz, 1H), 7.87 (d, J =
			7.9 Hz, 1H), 7.37 (d, J = 8.2 Hz, 3H), 7.25
			(t, J = 5.0 Hz, 2H), 6.88 (d, J = 8.1 Hz,
			2H), 6.28 (s, 1H), 6.21 (d, J = 8.1 Hz, 1H),
			4.31 (d, J = 8.5 Hz, 1H), 4.16 (d, J = 5.8
			Hz, 2H), 3.97 (d, J = 8.3 Hz, 1H), 2.40 (s,
			2H), 2.22 (s, 2H), 2.12 (p, J = 10.4, 9.5
			Hz, 2H), 1.86 (dd, J = 15.5, 8.8 Hz, 2H).
209	2- (dimethyla- mino)benzo- ic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-(dimethylamino)benzamide.
			LRMS (APCI) m/z 441 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 9.06 (d, J = 7.5
			Hz, 1H), 8.14 (t, J = 2.0 Hz, 1H), 7.60 (d,
			J = 7.7 Hz, 1H), 7.43 (s, 1H), 7.41-7.33
			(m, 2H), 7.25 (d, J = 8.2 Hz, 2H), 7.09 (s,
			1H), 6.30-6.17 (m, 2H), 4.29 (q, J = 7.7
			Hz, 1H), 4.16 (d, J = 4.9 Hz, 2H), 4.03-
			3.91 (m, 1H), 2.79 (s, 6H), 2.39 (s, 2H),
			2.22 (d, J = 9.0 Hz, 2H), 2.03 (q, J = 11.3
			Hz, 2H), 1.91-1.78 (m, 2H).
212	2- cyanobenzo- ic acid	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)-2-cyanobenzamide. LRMS (APCI)
			m/z 423 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.85 (d, J = 7.4 Hz, 1H),
			7.96-7.84 (m, 1H), 7.82-7.70 (m, 2H),
			7.67 (ddd, J = 7.7, 6.2, 2.6 Hz, 1H), 7.42-
			7.32 (m, 2H), 7.30-7.21 (m, 2H), 6.28 (t,
			J = 6.0 Hz, 1H), 6.21 (d, J = 8.1 Hz, 1H),
			4.29 (p, J = 8.0 Hz, 1H), 4.17 (d, J = 6.0
			Hz, 2H), 3.97 (q, J = 8.0 Hz, 1H), 2.45-
			2.36 (m, 2H), 2.22 (ddt, J = 17.9, 12.0, 6.5
			Hz, 2H), 2.07 (ddd, J = 16.3, 10.6, 8.6 Hz,
			2H), 1.93-1.77 (m, 2H).
159	4- methylbenzo- ic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(4-
			methylbenzoyl)-6-azaspiro[3.4]octan-2-
			yl)urea. LRMS (APCI) m/z 412 (M + H).
			1H NMR (400 MHz, Chloroform-d) δ 7.43
			(dd, J = 8.0, 3.2 Hz, 1H), 7.40-7.31 (m,
			2H), 7.21 (dt, J = 15.1, 7.9 Hz, 3H), 5.05
			(t, J = 8.3 Hz, 1H), 4.78 (s, 1H), 4.40 (d, J =
			5.7 Hz, 1H), 4.32 (s, 2H), 3.54 (d, J =
			24.4 Hz, 5H), 2.44 (s, 3H), 2.26 (s, 2H),
			1.99 (s, 5H).
160	2- methylisoni- cotinic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(2-
			methylisonicotinoyl)-6-
			azaspiro[3.4]octan-2-yl)urea. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.52 (t, J = 4.6 Hz,
			1H), 7.40-7.31 (m, 3H), 7.29-7.20 (m,
			3H), 6.35 (d, J = 2.8 Hz, 1H), 6.14 (d, J =
			8.1 Hz, 1H), 4.16 (dd, J = 14.2, 6.0 Hz,
			2H), 4.12-4.03 (m, 2H), 3.48 (t, J = 6.9
			Hz, 1H), 3.43-3.34 (m, 2H), 3.27 (s,
			1H), 3.17 (d, J = 5.0 Hz, 2H), 2.29-2.12
			(m, 2H), 1.97-1.85 (m, 3H), 1.80 (td, J =
			8.7, 2.7 Hz, 1H).
161	3- methylbenzo- ic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(3-
			methylbenzoyl)-6-azaspiro[3.4]octan-2-
			yl)urea. LRMS (APCI) m/z 412 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.41-
			7.32 (m, 4H), 7.32-7.17 (m, 4H), 6.33
			(d, J = 7.9 Hz, 1H), 6.14 (d, J = 8.2 Hz,
			1H), 4.16 (dd, J = 15.8, 6.0 Hz, 2H), 4.10-
			4.01 (m, 1H), 3.47 (t, J = 6.9 Hz, 1H),
			3.43-3.36 (m, 2H), 2.34 (d, J = 2.1 Hz,
			3H), 2.24 (t, J = 9.8 Hz, 1H), 2.16 (t, J =
			9.9 Hz, 1H), 1.92 (t, J = 6.6 Hz, 2H), 1.88-
			1.82 (m, 1H), 1.78 (dd, J = 11.7, 8.7 Hz,
			2H).
162	2- methylbenzo- ic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(2-
			methylbenzoyl)-6-azaspiro[3.4]octan-2-
			yl)urea. LRMS (APCI) m/z 412 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.40-
			7.33 (m, 2H), 7.32-7.19 (m, 5H), 7.19-
			7.14 (m, 1H), 6.33 (dd, J = 10.4, 6.0 Hz,
			1H), 6.15 (d, J = 8.1 Hz, 1H), 4.16 (dd, J =
			14.5, 6.0 Hz, 2H), 4.12-4.01 (m, 1H),
			3.49 (t, J = 7.0 Hz, 1H), 3.42 (s, 1H), 3.17
			(d, J = 5.0 Hz, 1H), 3.05 (t, J = 6.7 Hz,
			1H), 2.28-2.13 (m, 5H), 1.89 (dt, J =
			26.9, 6.8 Hz, 3H), 1.80-1.73 (m, 1H).
163	4- methoxyben- zoic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(4-
			methoxybenzoyl)-6-azaspiro[3.4]octan-
			2-yl)urea. LRMS (APCI) m/z 428
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.52-7.47 (m, 2H), 7.36 (t, J = 8.3 Hz,
			2H), 7.28-7.20 (m, 2H), 6.97 (d, J = 8.1
			Hz, 2H), 6.39-6.26 (m, 1H), 6.14 (d, J =
			8.1 Hz, 1H), 4.16 (dd, J = 14.8, 6.0 Hz,
			2H), 4.12-4.01 (m, 1H), 3.80 (s, 3H),
			3.46 (t, J = 6.8 Hz, 2H), 3.38 (s, 2H), 2.24
			(s, 1H), 2.16 (t, J = 9.9 Hz, 1H), 1.96-
			1.83 (m, 3H), 1.78 (t, J = 9.6 Hz, 1H).
166	3- methylisoni- cotinic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(3-
			methylisonicotinoyl)-6-
			azaspiro[3.4]octan-2-yl)urea. LRMS
			(APCI) m/z 413 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.57 (s, 1H), 8.51 (d, J =
			5.0 Hz, 1H), 7.41-7.29 (m, 3H), 7.29-
			7.19 (m, 2H), 6.38-6.30 (m, 1H), 6.14
			(d, J = 8.1 Hz, 1H), 4.16 (dd, J = 13.2, 5.8
			Hz, 2H), 4.07 (q, J = 7.9 Hz, 1H), 3.51 (t,
			J = 7.0 Hz, 1H), 3.44 (s, 1H), 3.08 (t, J =
			6.7 Hz, 1H), 2.99 (s, 1H), 2.29-2.11 (m,
			5H), 1.91 (dt, J = 22.0, 7.0 Hz, 3H), 1.78
			(dd, J = 11.8, 8.6 Hz, 1H).
167	4- fluorobenzo- ic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(4-
			fluorobenzoyl)-6-azaspiro[3.4]octan-2-
			yl)urea. LRMS (APCI) m/z 416 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.63-
			7.55 (m, 2H), 7.40-7.33 (m, 2H), 7.25
			(dtd, J = 12.6, 6.0, 3.1 Hz, 4H), 6.34 (t, J =
			6.8 Hz, 1H), 6.14 (d, J = 8.1 Hz, 1H),
			4.16 (dd, J = 14.8, 5.9 Hz, 2H), 4.08 (p, J =
			7.9 Hz, 1H), 3.48 (t, J = 6.9 Hz, 1H),
			3.45-3.37 (m, 2H), 3.33 (s, 1H), 2.24
			(dd, J = 11.4, 8.3 Hz, 1H), 2.21-2.11 (m,
			1H), 1.90 (dt, J = 21.9, 6.7 Hz, 3H), 1.79
			(dd, J = 11.7, 8.6 Hz, 1H).
169	3- isopropylben- zoic acid	3.5
			1-(4-chlorobenzyl)-3-((2r,4s)-6-(3-
			isopropylbenzoyl)-6-azaspiro[3.4]octan-
			2-yl)urea. LRMS (APCI) m/z 440
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.41-7.28 (m, 5H), 7.24 (dd, J = 14.3,
			8.3 Hz, 3H), 6.33 (q, J = 8.6, 7.4 Hz, 1H),
			6.14 (d, J = 8.2 Hz, 1H), 4.16 (dd, J =
			16.5, 5.9 Hz, 2H), 4.07 (dq, J = 8.6, 5.2
			Hz, 1H), 3.48 (t, J = 6.9 Hz, 1H), 3.43-
			3.28 (m, 4H), 2.93 (p, J = 6.9 Hz, 1H),
			2.29-2.20 (m, 1H), 2.20-2.12 (m, 1H),
			1.89 (dt, J = 24.7, 6.7 Hz, 2H), 1.78 (dd, J =
			11.8, 8.7 Hz, 1H), 1.22 (dd, J = 6.9, 2.2
			Hz, 6H).
164	4- methylbenzo- ic acid	3.6
			1-(4-chlorobenzyl)-3-((2s,4r)-6-(4-
			methylbenzoyl)-6-azaspiro[3.4]octan-2-
			yl)urea. LRMS (APCI) m/z 412 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.41 (d,
			J = 7.9 Hz, 2H), 7.36 (t, J = 8.6 Hz, 2H),
			7.29-7.19 (m, 4H), 6.29 (dd, J = 14.6,
			7.8 Hz, 2H), 4.16 (dd, J = 16.3, 5.9 Hz,
			2H), 4.09 (d, J = 8.2 Hz, 1H), 3.96-3.84
			(m, 1H), 3.45-3.39 (m, 1H), 2.38-2.27
			(m, 4H), 2.13 (t, J = 9.8 Hz, 2H), 1.90-
			1.73 (m, 4H), 1.12 (s, 1H).
165	4- methoxyben- zoic acid	3.6
			1-(4-chlorobenzyl)-3-((2s,4r)-6-(4-
			methoxybenzoyl)-6-azaspiro[3.4]octan-
			2-yl)urea. LRMS (APCI) m/z 428
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.54-7.46 (m, 2H), 7.35 (d, J = 8.0 Hz,
			2H), 7.24 (t, J = 10.9 Hz, 2H), 6.98 (d, J =
			8.1 Hz, 2H), 6.30 (dd, J = 13.5, 7.7 Hz,
			2H), 4.23-4.05 (m, 3H), 3.80 (s, 3H),
			3.50-3.38 (m, 4H), 2.32 (d, J = 9.3 Hz,
			1H), 2.14 (t, J = 9.7 Hz, 1H), 1.84 (dt, J =
			16.3, 7.8 Hz, 4H).
354	[1,4′- bipiperidine]- 1′- carboxylic acid	3.5
			1-((2r,4s)-6-([1,4′-bipiperidine]-1′-
			carbonyl)-6-azaspiro[3.4]octan-2-yl)-3-(4-
			chlorobenzyl)urea. LRMS (APCI) m/z
			488.1 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.32 (d, J = 8.2 Hz, 2 H),
			7.27 (d, J = 8.2 Hz, 2 H), 4.29 (s, 2 H),
			4.17 (p, J = 8.2 Hz, 1 H), 3.93 (d, J = 13.6
			Hz, 2 H), 3.43 (t, J = 6.7 Hz, 2 H), 3.34-
			3.30 (m, 7 H), 2.85 (t, J = 12.8 Hz, 2 H),
			2.33 (t, J = 10.2 Hz, 2 H), 2.08 (d, J = 12.1
			Hz, 2 H), 1.99-1.81 (m, 8 H), 1.79-1.61
			(m, 4 H).
240	6- methylnico- tinic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-6-methylnicotinamide.
			LRMS (APCI) m/z 427.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 8.72 (d,
			J = 2.2 Hz, 1H), 8.00 (dd, J = 8.2, 2.2 Hz,
			1H), 7.29 (d, J = 8.2 Hz, 1H), 7.19 (d, J =
			8.2 Hz, 2H), 7.13 (d, J = 8.2 Hz, 2H), 4.16
			(s, 2H), 3.91 (p, J = 8.0 Hz, 1H), 3.27 (d,
			J = 7.2 Hz, 2H), 2.48 (s, 3H), 2.40 (dd, J =
			15.2, 7.6 Hz, 2H), 2.34 (dd, J = 10.7,
			5.7 Hz, 1H), 2.21 (dt, J = 12.1, 6.2 Hz,
			1H), 2.11 (td, J = 9.6, 7.9, 3.4 Hz, 1H),
			1.72 (ddd, J = 30.9, 11.4, 8.0 Hz, 4H).
243	tetrahydro- 2H- thiopyran- 4- carboxylic acid 1,1- dioxide	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)tetrahydro-2H-thiopyran-
			4-carboxamide 1,1-dioxide. LRMS
			(APCI) m/z 468.1 (M + H). 1H NMR (400
			MHz, Methanol-d4) δ 7.31 (d, J = 8.2 Hz,
			2H), 7.26 (d, J = 8.2 Hz, 2H), 4.28 (s,
			2H), 4.02 (p, J = 8.2 Hz, 1H), 3.23-3.06
			(m, 6H), 2.47 (ddq, J = 28.5, 11.7, 5.7 Hz,
			2H), 2.40-2.12 (m, 7H), 2.02 (ddd, J =
			11.5, 7,9, 3.5 Hz, 1H), 1.90-1.75 (m,
			3H), 1.71 (dd, J = 11.0, 8.1 Hz, 1H).
255	6- methylnico- tinic acid	15.1
			N-(1-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)ethyl)-6-methylnicotinamide
			LRMS (APCI) m/z 441.1 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.11 (t, J =
			9.2 Hz, 1H), 7.99 (ddd, J = 8.1, 3.8, 2.3
			Hz, 1H), 7.32-7.23 (m, 3H), 7.16 (d, J =
			8.4 Hz, 2H), 6.22-6.13 (m, 1H), 6.10 (d,
			J = 8.0 Hz, 1H), 4.07 (d, J = 6.1 Hz, 2H),
			3.85 (ddt, J = 23.4, 16.0, 8.9 Hz, 2H), 2.20
			(dq, J = 25.0, 8.1 Hz, 2H), 2.09-1.91 (m,
			2H), 1.72-1.56 (m, 4H), 1.19-1.04 (m,
			5H), 0.95 (dd, J = 6.6, 3.5 Hz, 3H).
245	6- methylpico- linic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-6-methylpicolinamide.
			LRMS (APCI) m/z 427.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.48 (dd, J =
			4.8, 1.8 Hz, 1H), 8.40 (t, J = 5.8 Hz,
			1H), 7.64 (dd, J = 7.7, 1.8 Hz, 1H), 7.40-
			7.32 (m, 2H), 7.30-7.21 (m, 3H), 6.26 (t,
			J = 6.1 Hz, 1H), 6.17 (d, J = 8.1 Hz, 1H),
			4.16 (d, J = 6.0 Hz, 2H), 3.92 (h, J = 8.2
			Hz, 1H), 3.23 (t, J = 6.5 Hz, 2H), 2.35
			(ddd, J = 27.2, 13.3, 7.3 Hz, 3H), 2.25-
			2.05 (m, 3H), 1.97 (ddd, J = 11.4, 7.9, 3.3
			Hz, 1H), 1.79 (dd, J = 7.8, 4.3 Hz, 2H),
			1.78-1.67 (m, 3H).
246	2- methylisoni- cotinic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-2-methylisonicotinamide.
			LRMS (APCI) m/z 427.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.65 (t, J =
			5.7 Hz, 1H), 8.56 (d, J = 5.1 Hz, 1H), 7.60
			(d, J = 1.6 Hz, 1H), 7.52 (dd, J = 5.2, 1.6
			Hz, 1H), 7.40-7.32 (m, 2H), 7.27-7.20
			(m, 2H), 6.25 (t, J = 6.1 Hz, 1H), 6.17 (d,
			J = 8.0 Hz, 1H), 4.15 (d, J = 6.0 Hz, 2H),
			4.10 (d, J = 5.5 Hz, 1H), 3.91 (h, J = 8.2
			Hz, 1H), 3.26 (t, J = 6.5 Hz, 2H), 3.17 (d,
			J = 4.1 Hz, 2H), 2.41-2.27 (m, 2H), 2.20
			(ddd, J = 12.1, 7.3, 5.1 Hz, 1H), 2.09
			(ddd, J = 11.2, 7.9, 3.2 Hz, 1H), 1.96
			(ddd, J = 11.3, 7.9, 3.1 Hz, 1H), 1.77 (dd,
			J = 10.5, 8.5 Hz, 3H), 1.73-1.66 (m,
			1H).
247	1H- pyrazole-4- carboxylic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-1H-pyrazole-4-
			carboxamide. LRMS (APCI) m/z 402.1
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 13.07 (s, 1H), 8.14 (s, 1H), 7.97 (t, J =
			5.8 Hz, 1H), 7.86 (s, 1H), 7.36 (d, J = 8.4
			Hz, 2H), 7.24 (d, J = 8.2 Hz, 2H), 6.24 (t,
			J = 6.1 Hz, 1H), 6.16 (d, J = 8.1 Hz, 1H),
			4.15 (d, J = 6.0 Hz, 2H), 3.90 (h, J = 8.3
			Hz, 1H), 3.18 (dd, J = 8.1, 5.9 Hz, 2H),
			2.32 (dq, J = 19.4, 10.8, 9.3 Hz, 2H), 2.23-
			2.14 (m, 1H), 2.07 (ddd, J = 11.2, 8.0,
			3.1 Hz, 1H), 1.94 (ddd, J = 11.3, 7.9, 3.0
			Hz, 1H), 1.80-1.70 (m, 3H), 1.67 (dd, J =
			11.4, 7.4 Hz, 1H).
248	6- methylnico- tinic acid	16.1
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-N,6-dimethylnicotinamide.
			LRMS (APCI) m/z 441.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.50-8.36
			(m, 1H), 7.81-7.64 (m, 1H), 7.32 (dd, J =
			14.7, 8.1 Hz, 3H), 7.17 (d, J = 8.0 Hz,
			2H), 6.28-6.16 (m, 1H), 6.11 (d, J = 20.2
			Hz, 1H), 4.15-4.01 (m, 2H), 3.94-3.70
			(m, 2H), 3.20-3.15 (m, 1H), 2.85 (s,
			1H), 2.80 (s, 1H), 2.47 (s, 3H), 2.37-
			2.18 (m, 2H), 2.16-2.06 (m, 1H), 1.95
			(dd, J = 14.4, 7.5 Hz, 1H), 1.88-1.53 (m,
			4H), 1.53-1.29 (m, 2H).
250	tetrahydro- 2H-pyran- 4- carboxylic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)tetrahydro-2H-pyran-4-
			carboxamide. LRMS (APCI) m/z 420.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.73 (t, J = 5.8 Hz, 1H), 7.36 (d, J = 8.4
			Hz, 2H), 7.23 (d, J = 8.3 Hz, 2H), 6.25 (t,
			J = 5.9 Hz, 1H), 6.16 (d, J = 8.1 Hz, 1H),
			4.15 (d, J = 6.0 Hz, 2H), 3.95-3.87 (m,
			1H), 3.84 (dt, J = 11.2, 3.3 Hz, 2H), 3.32-
			3.24 (m, 2H), 3.02 (t, J = 6.4 Hz, 2H),
			2.37-2.27 (m, 2H), 2.23 (dd, J = 15.5,
			7.5 Hz, 1H), 2.15 (dt, J = 11.8, 6.3 Hz,
			1H), 2.02 (t, J = 9.5 Hz, 1H), 1.93-1.84
			(m, 1H), 1.80-1.65 (m, 3H), 1.64-1.56
			(m, 2H), 1.54 (dd, J = 8.5, 3.6 Hz, 3H).
251	cyclopentane- carboxylic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)cyclopentanecarboxamide.
			LRMS (APCI) m/z 404.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.69 (t, J =
			5.7 Hz, 1H), 7.40-7.32 (m, 2H), 7.28-
			7.20 (m, 2H), 6.25 (t, J = 6.1 Hz, 1H),
			6.15 (d, J = 8.1 Hz, 1H), 4.15 (d, J = 6.0
			Hz, 2H), 3.89 (h, J = 8.2 Hz, 1H), 3.09-
			2.95 (m, 2H), 2.22 (dddd, J = 29.7, 23.0,
			12.1, 5.5 Hz, 4H), 2.03 (ddd, J = 11.1, 8.0,
			3.2 Hz, 1H), 1.89 (ddd, J = 11.4, 8.0, 3.2
			Hz, 1H), 1.80-1.65 (m, 5H), 1.59 (ttd, J =
			11.5, 7.8, 3.5 Hz, 5H), 1.48 (td, J = 5.5,
			5.1, 2.4 Hz, 2H).
252	2- oxopiperidine- 4- carboxylic acid	12.2
			N-((6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-
			2-yl)methyl)-2-oxopiperidine-4-
			carboxamide. LRMS (APCI) m/z 433.2
			(M + H). 1H NMR (DMSO-d6) δ: 7.89-
			7.81 (m, 1H), 7.45 (d, J = 2.7 Hz, 1H),
			7.40-7.32 (m, 2H), 7.27-7.20 (m, 2H),
			6.26 (t, J = 6.2 Hz, 1H), 6.17 (d, J = 8.1
			Hz, 1H), 4.15 (d, J = 6.1 Hz, 2H), 3.90 (h,
			J = 8.2 Hz, 1H), 3.15-2.94 (m, 5H), 2.59
			(tdd, J = 9.6, 6.1, 3.4 Hz, 1H), 2.33-2.10
			(m, 5H), 2.04 (ddd, J = 11.1, 7.8, 3.2 Hz,
			1H), 1.90 (ddd, J = 11.3, 7.8, 3.2 Hz, 1H),
			1.85-1.55 (m, 5H).
275	2- methylbenzo- ic acid	3.7
			N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-
			2-methylbenzamide. LRMS (APCI) m/z
			388.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.19 (t, J = 5.6 Hz, 1H), 7.37
			(d, J = 8.0 Hz, 2H), 7.34-7.17 (m 6H),
			6.31 (t, J = 5.7 Hz, 1H), 5.98-5.91 (m,
			1H), 4.18 (d, J = 5.7 Hz, 2H), 3.24-3.16
			(m, 2H), 3.01 (q, J = 6.3 Hz, 2H), 2.32 (s,
			3H), 1.51 (p, J = 7.2 Hz, 2H), 1.41 (p, J =
			7.0 Hz, 2H), 1.32 (q, J = 7.1, 6.5 Hz, 2H).
276	3- methylbenzo- ic acid	3.7
			N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-
			3-methylbenzamide. LRMS (APCI) m/z
			388.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.37 (t, J = 5.6 Hz, 1H), 7.67-
			7.59 (m, 2H), 7.34 (dd, J = 13.3, 6.5 Hz,
			4H), 7.25 (d, J = 8.1 Hz, 1H), 6.31 (t, J =
			6.2 Hz, 1H), 5.95 (d, J = 5.9 Hz, 1H), 4.17
			(d, J = 5.9 Hz, 2H), 3.24 (q, J = 6.6 Hz,
			2H), 3.01 (q, J = 6.4 Hz, 2H), 2.35 (s,
			4H), 1.52 (p, J = 7.1 Hz, 2H), 1.41 (p, J =
			7.2 Hz, 2H), 1.30 (q, J = 7.9 Hz, 2H).
277	nicotinic acid	3.7
			N-(5-(3-(4-
			chlorobenzyl)ureido)pentyl)nicotinamide.
			LRMS (APCI) m/z 375.1 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 9.00 (d, J =
			2.1 Hz, 1H), 8.71 (d, J = 4.8 Hz, 1H),
			8.64 (s, 1H), 8.24-8.16 (m, 1H), 7.52
			(dd, J = 8.0, 4.9 Hz, 1H), 7.36 (d, J = 8.1
			Hz, 2H), 7.25 (d, J = 8.1 Hz, 2H), 6.31 (s,
			1H), 5.95 (s, 1H), 4.17 (d, J = 5.2 Hz,
			2H), 3.27 (q, J = 6.6 Hz, 2H), 3.01 (q, J =
			6.2, 5.8 Hz, 2H), 1.54 (p, J = 7.2 Hz, 2H),
			1.41 (p, J = 6.9 Hz, 2H), 1.31 (q, J = 7.7
			Hz, 2H).
279	picolinic acid	3.7
			N-(5-(3-(4-
			chlorobenzyl)ureido)pentyl)picolinamide.
			LRMS (APCI) m/z 375.0 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.76 (d, J =
			6.3 Hz, 1H), 8.64 (d, J = 4.8 Hz, 1H),
			8.01 (dt, J = 15.1, 7.7 Hz, 2H), 7.60 (t, J =
			6.1 Hz, 1H), 7.36 (d, J = 8.2 Hz, 2H), 7.25
			(d, J = 8.1 Hz, 2H), 6.30 (t, J = 6.2 Hz,
			1H), 6.01-5.86 (m, 1H), 4.17 (d, J = 5.8
			Hz, 2H), 3.29 (d, J = 6.7 Hz, 2H), 3.00 (q,
			J = 6.5 Hz, 2H), 1.54 (p, J = 7.3 Hz, 2H),
			1.40 (p, J = 7.0 Hz, 2H), 1.28 (p, J = 7.7
			Hz, 2H).
280	2- fluorobenzo- ic acid	3.7
			N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-
			2-fluorobenzamide. LRMS (APCI) m/z
			392.0 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.29 (s, 1H), 7.54 (dt, J =
			31.2, 7.3 Hz, 2H), 7.36 (d, J = 8.0 Hz,
			2H), 7.25 (d, J = 8.0 Hz, 4H), 6.31 (t, J =
			6.2 Hz, 1H), 5.95 (t, J = 5.8 Hz, 1H), 4.17
			(d, J = 5.9 Hz, 2H), 3.23 (q, J = 6.6 Hz,
			2H), 3.01 (q, J = 6.5 Hz, 2H), 1.51 (p, J =
			7.1 Hz, 2H), 1.41 (p, J = 7.0 Hz, 2H), 1.30
			(p, J = 7.4 Hz, 2H).
281	6- methylnico- tinic acid	3.7
			N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-
			6-methylnicotinamide. LRMS (APCI)
			m/z 389.0 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.89 (d, J = 2.2 Hz, 1H),
			8.56 (t, J = 5.6 Hz, 1H), 8.11 (dd, J = 8.1,
			2.2 Hz, 1H), 7.42-7.31 (m, 3H), 7.25 (d,
			J = 8.1 Hz, 2H), 6.32 (d, J = 6.5 Hz, 1H),
			5.95 (s, 1H), 4.17 (d, J = 5.7 Hz, 2H), 3.26
			(q, J = 6.7 Hz, 2H), 3.01 (q, J = 6.3 Hz,
			2H), 2.53 (s, 3H), 1.53 (p, J = 7.3 Hz,
			2H), 1.41 (p, J = 7.0 Hz, 2H), 1.31 (q, J =
			7.8 Hz, 2H).
283	2-(pyridin- 3-yl)acetic acid	3.7
			N-(5-(3-(4-chlorobenzyl)ureido)pentyl)-
			2-(pyridin-3-yl)acetamide. LRMS
			(APCI) m/z 389.1 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.49 (s, 2H), 8.11 (q, J =
			6.6, 5.6 Hz, 1H), 7.74 (d, J = 7.9 Hz,
			1H), 7.46-7.31 (m, 3H), 7.25 (d, J = 8.1
			Hz, 2H), 6.31 (t, J = 6.2 Hz, 1H), 5.98-
			5.88 (m, 1H), 4.18 (d, J = 5.8 Hz, 2H),
			3.46 (s, 3H), 3.01 (dq, J = 24.4, 6.6 Hz,
			4H), 1.38 (dp, J = 14.7, 7.1 Hz, 4H), 1.24
			(q, J = 8.1 Hz, 2H).
289	nicotinic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-
			nicotinoylpiperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 429.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.63 (d, J =
			23.7 Hz, 2H), 7.81 (d, J = 7.8 Hz, 1H),
			7.48 (dd, J = 8.0, 4.7 Hz, 1H), 7.36 (d, J =
			8.3 Hz, 2H), 7.25 (d, J = 8.2 Hz, 2H), 6.31
			(t, J = 6.2 Hz, 1H), 5.93 (t, J = 5.7 Hz,
			1H), 4.46 (s, 1H), 4.17 (d, J = 6.1 Hz,
			2H), 4.09 (s, 1H), 3.49 (s, 1H), 3.17 (s,
			3H), 3.00 (q, J = 6.5 Hz, 2H), 2.76 (s,
			1H), 1.74 (s, 1H), 1.60 (s, 1H), 1.49 (s,
			1H), 1.41-1.30 (m, 2H), 1.26-1.22 (m,
			2H), 1.08 (s, 1H).
290	isonicotinic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-
			isonicotinoylpiperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 429.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.70 (s,
			1H), 7.40-7.32 (m, 4H), 7.25 (d, J = 8.1
			Hz, 2H), 6.32 (t, J = 6.2 Hz, 1H), 5.93 (t,
			J = 5.7 Hz, 1H), 4.45 (d, J = 13.0 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.40 (d, J = 13.8
			Hz, 2H), 3.18 (s, 3H), 2.75 (t, J = 12.4 Hz,
			1H), 1.74 (d, J = 13.2 Hz, 1H), 1.58 (d, J =
			13.0 Hz, 1H), 1.49 (s, 1H), 1.35 (q, J =
			7.0 Hz, 2H), 1.25 (d, J = 10.0 Hz, 4H),
			1.08 (ddd, J = 19.5, 12.8, 8.6 Hz, 2H).
292	picolinic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-
			picolinoylpiperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 429.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.58 (d, J =
			4.9 Hz, 1H), 7.91 (t, J = 7.7 Hz, 1H),
			7.55-7.42 (m, 2H), 7.35 (d, J = 8.0 Hz,
			2H), 7.25 (d, J = 8.1 Hz, 2H), 6.31 (t, J =
			6.1 Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H), 4.48
			(d, J = 13.2 Hz, 1H), 4.17 (d, J = 5.9 Hz,
			2H), 3.60 (d, J = 13.3 Hz, 1H), 3.00 (q, J =
			5.5 Hz, 3H), 2.75 (td, J = 12.8, 2.8 Hz,
			1H), 1.75 (d, J = 13.3 Hz, 1H), 1.62-
			1.46 (m, 2H), 1.36 (t, J = 7.1 Hz, 2H),
			1.25 (tt, J = 10.3, 6.6, 6.2 Hz, 4H), 1.14-
			1.00 (m, 2H).
291	2- phenylacetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-
			phenylacetyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 442.1 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.36 (d, J =
			8.2 Hz, 2H), 7.34-7.15 (m, 7H), 6.30
			(t, J = 6.1 Hz, 1H), 5.91 (t, J = 5.7 Hz,
			1H), 4.38 (d, J = 13.0 Hz, 1H), 4.17 (d, J =
			6.1 Hz, 2H), 3.95-3.82 (m, 1H), 3.69
			(s, 2H), 3.18 (s, 2H), 3.03-2.87 (m, 3H),
			1.59 (dd, J = 25.2, 13.1 Hz, 2H), 1.38-
			1.22 (m, 3H), 1.22-1.11 (m, 3H), 0.84
			(dtd, J = 28.7, 12.4, 6.3 Hz, 2H).
294	2-(pyridin- 3-yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(pyridin-
			3-yl)acetyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 443.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.44 (s,
			1H), 7.62 (d, J = 7.8 Hz, 1H), 7.40-7.30
			(m, 3H), 7.26 (d, J = 8.0 Hz, 2H), 6.31 (t,
			J = 6.1 Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H),
			5.76 (s, 1H), 4.36 (d, J = 13.2 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.97 (d, J = 13.6
			Hz, 1H), 3.74 (s, 2H), 2.99 (q, J = 7.4 Hz,
			3H), 2.55 (d, J = 13.7 Hz, 1H), 1.69-
			1.60 (m, 2H), 1.43 (s, 1H), 1.34 (q, J = 7.0
			Hz, 2H), 1.26 (q, J = 7.9, 7.2 Hz, 2H),
			1.18 (h, J = 6.0, 5.0 Hz, 2H), 0.92 (qt, J =
			12.4, 6.2 Hz, 2H).
295	2-(pyridin- 4-yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(pyridin-
			4-yl)acetyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 443.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.53 (s,
			1H), 7.36 (d, J = 8.1 Hz, 2H), 7.27 (t, J =
			9.1 Hz, 4H), 6.31 (t, J = 6.1 Hz, 1H), 5.93
			(t, J = 5.7 Hz, 1H), 5.76 (s, 1H), 4.36 (d, J =
			13.1 Hz, 1H), 4.17 (d, J = 5.9 Hz, 2H),
			3.90 (d, J = 13.7 Hz, 1H), 3.77 (s, 2H),
			3.04-2.91 (m, 3H), 1.63 (s, 2H), 1.48-
			1.25 (m, 4H), 1.25-1.12 (m, 4H), 0.90
			(q, J = 11.5 Hz, 2H).
296	2-(m- tolyl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(3-
			methylbenzoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 442.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.35 (d, J = 8.1 Hz, 2H), 7.33-7.22 (m,
			4H), 7.19-7.10 (m, 2H), 6.31 (t, J = 6.2
			Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H), 4.45 (s,
			1H), 4.17 (d, J = 6.0 Hz, 2H), 3.55 (s,
			1H), 3.33 (s, 3H), 3.00 (q, J = 6.5 Hz,
			2H), 2.70 (d, J = 17.5 Hz, 1H), 2.33 (s,
			3H), 1.81-1.66 (m, 1H), 1.66-1.54 (m,
			1H), 1.47 (dt, J = 10.1, 6.5 Hz, 1H), 1.35
			(q, J = 6.5 Hz, 2H), 1.23 (s, 4H), 1.14-
			0.93 (m, 2H).
297	2-(o- tolyl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-
			methylbenzoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 442.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.35 (d, J = 8.1 Hz, 2H), 7.32-7.18 (m,
			5H), 7.18-7.05 (m, 1H), 6.30 (t, J = 6.3
			Hz, 1H), 5.92 (t, J = 5.7 Hz, 1H), 4.52 (d,
			J = 13.0 Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H),
			3.27-3.14 (m, 1H), 3.05-2.85 (m, 3H),
			2.72 (t, J = 13.2 Hz, 1H), 2.20 (d, J = 20.0
			Hz, 3H), 1.74 (d, J = 12.9 Hz, 1H), 1.65-
			1.40 (m, 3H), 1.34 (q, J = 6.2, 5.4 Hz,
			2H), 1.30-1.14 (m, 4H), 1.14-0.81 (m,
			3H).
298	2-(6- methylpyri- din-2- yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(6-
			methylpicolinoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 443.3
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.78 (t, J = 7.6 Hz, 1H), 7.39-7.22 (m,
			6H), 6.31 (t, J = 6.1 Hz, 1H), 5.93 (t, J =
			5.8 Hz, 1H), 4.47 (d, J = 12.8 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.57 (d, J = 13.4
			Hz, 1H), 3.05-2.91 (m, 3H), 2.74 (t, J =
			12.3 Hz, 1H), 2.48 (s, 3H), 1.75 (d, J =
			13.1 Hz, 1H), 1.57 (d, J = 13.4 Hz, 1H),
			1.49 (s, 1H), 1.36 (s, 2H), 1.24 (s, 4H),
			1.04 (s, 2H).
299	2-(6- methylpyri- din-2- yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(6-
			methylpyridin-2-yl)acetyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 457.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.62 (t, J = 7.8 Hz, 1H), 7.36 (d, J = 8.1
			Hz, 2H), 7.25 (d, J = 8.1 Hz, 2H), 7.09
			(dd, J = 18.8, 7.7 Hz, 2H), 6.31 (t, J = 6.1
			Hz, 1H), 5.92 (t, J = 5.8 Hz, 1H), 4.35 (s,
			1H), 4.17 (d, J = 6.0 Hz, 2H), 3.98 (d, J =
			13.6 Hz, 1H), 3.80 (d, J = 4.4 Hz, 2H),
			3.17 (s, 1H), 3.04-2.90 (m, 3H), 2.43 (s,
			3H), 1.61 (t, J = 14.7 Hz, 2H), 1.42 (s,
			1H), 1.35 (t, J = 7.1 Hz, 2H), 1.24 (s, 2H),
			1.18 (d, J = 6.5 Hz, 2H), 0.91 (q, J = 9.2,
			6.7 Hz, 2H).
300	tetrahydro- 2H-pyran- 4- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(tetrahydro-
			2H-pyran-4-carbonyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 436.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.36 (d, J = 8.1 Hz, 2H), 7.26 (d, J = 8.1
			Hz, 2H), 6.31 (t, J = 6.1 Hz, 1H), 5.93 (t,
			J = 5.8 Hz, 1H), 4.37 (d, J = 13.1 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.94 (d, J = 13.7
			Hz, 1H), 3.83 (dt, J = 11.6, 3.0 Hz, 2H),
			3.39 (d, J = 11.5 Hz, 2H), 2.98 (dd, J =
			12.3, 5.5 Hz, 3H), 2.90-2.77 (m, 1H),
			2.47 (t, J = 11.9 Hz, 1H), 1.73-1.53 (m,
			3H), 1.53-1.40 (m, 4H), 1.35 (p, J = 7.2
			Hz, 2H), 1.24 (ddd, J = 28.2, 13.9, 6.9 Hz,
			3H), 1.05-0.81 (m, 2H).
301	2- oxopiperidine- 4- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-
			oxopiperidine-4-carbonyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 449.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.43 (s, 1H), 7.36 (d, J = 8.1 Hz, 2H),
			7.26 (d, J = 8.1 Hz, 2H), 6.32 (t, J = 6.1
			Hz, 1H), 5.93 (t, J = 5.8 Hz, 1H), 4.37 (d,
			J = 13.0 Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H),
			3.93 (d, J = 13.4 Hz, 1H), 3.16-3.08 (m,
			3H), 3.00 (q, J = 6.3 Hz, 3H), 2.28-2.17
			(m, 1H), 2.12 (dd, J = 17.2, 5.5 Hz, 1H),
			1.78-1.73 (m, 1H), 1.65 (d, J = 18.6 Hz,
			4H), 1.43 (d, J = 11.0 Hz, 1H), 1.35 (q, J =
			7.0 Hz, 2H), 1.21 (d, J = 6.8 Hz, 4H),
			0.99 (d, J = 12.2 Hz, 1H), 0.91 (d, J =
			11.4 Hz, 1H).
302	1-methyl- 2- oxopiperidine- 4- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-2-
			oxopiperidine-4-carbonyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 463.3
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.36 (d, J = 8.1 Hz, 2H), 7.25 (d, J = 8.1
			Hz, 2H), 6.31 (t, J = 6.1 Hz, 1H), 5.93 (t,
			J = 5.8 Hz, 1H), 4.37 (d, J = 13.1 Hz, 1H),
			4.17 (d, J = 6.1 Hz, 2H), 3.92 (d, J = 13.5
			Hz, 1H), 3.31-3.23 (m, 1H), 3.18 (q, J =
			6.1, 3.5 Hz, 2H), 2.99 (q, J = 6.4 Hz, 3H),
			2.79 (s, 3H), 2.46 (s, 1H), 2.25 (dtd, J =
			22.8, 17.6, 7.4 Hz, 2H), 1.90-1.80 (m,
			1H), 1.64 (d, J = 16.5 Hz, 3H), 1.44 (s,
			1H), 1.35 (q, J = 6.6 Hz, 2H), 1.23 (dt, J =
			21.5, 8.7 Hz, 4H), 0.96 (dt, J = 41.5, 11.9
			Hz, 2H).
303	5- oxopyrrolidine- 3- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(5-
			oxopyrrolidine-3-carbonyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 435.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.57 (s, 1H), 7.36 (d, J = 8.1 Hz, 2H),
			7.25 (d, J = 8.1 Hz, 2H), 6.31 (t, J = 6.2
			Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H), 4.36 (d,
			J = 12.9 Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H),
			3.90-3.82 (m, 1H), 3.64-3.51 (m, 1H),
			3.41 (t, J = 9.1 Hz, 1H), 3.30-3.23 (m,
			1H), 3.17 (d, J = 4.9 Hz, 1H), 2.99 (q, J =
			7.2, 6.8 Hz, 3H), 2.40-2.24 (m, 2H),
			1.64 (d, J = 13.0 Hz, 2H), 1.44 (s, 1H),
			1.35 (t, J = 7.4 Hz, 2H), 1.24 (dd, J =
			22.2, 8.8 Hz, 4H), 0.95 (dt, J = 23.5, 12.5
			Hz, 2H).
304	1-methyl- 5- oxopyrrolidine- 3- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-5-
			oxopyrrolidine-3-carbonyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 449.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.36 (d, J = 8.1 Hz, 2H), 7.25 (d, J = 8.1
			Hz, 2H), 6.31 (t, J = 6.2 Hz, 1H), 5.93 (t,
			J = 5.8 Hz, 1H), 4.36 (d, J = 13.1 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.86 (d, J = 13.6
			Hz, 1H), 3.52 (t, J = 4.8 Hz, 2H), 3.17 (d,
			J = 4.2 Hz, 2H), 2.99 (q, J = 6.3 Hz, 3H),
			2.70 (s, 3H), 2.44 (d, J = 6.7 Hz, 2H), 1.65
			(d, J = 13.9 Hz, 2H), 1.45 (s, 1H), 1.35 (q,
			J = 6.8 Hz, 2H), 1.24 (dq, J = 21.0, 7.4,
			6.8 Hz, 4H), 1.05-0.85 (m, 2H).
305	oxazole-2- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(oxazole-2-
			carbonyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 419.1 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.28 (s,
			1H), 7.43 (s, 1H), 7.36 (d, J = 8.2 Hz,
			2H), 7.25 (d, J = 8.1 Hz, 2H), 6.31 (t, J =
			6.2 Hz, 1H), 5.93 (t, J = 5.8 Hz, 1H), 4.46
			(dd, J = 26.1, 13.3 Hz, 2H), 4.17 (d, J =
			6.0 Hz, 2H), 3.20-3.07 (m, 1H), 3.00 (q,
			J = 6.4 Hz, 2H), 2.80 (td, J = 12.8, 2.9 Hz,
			1H), 1.73 (t, J = 16.7 Hz, 2H), 1.62-1.44
			(m, 1H), 1.35 (q, J = 6.8 Hz, 2H), 1.32-
			1.17 (m, 4H), 1.08 (dddd, J = 24.4, 20.4,
			12.3, 6.1 Hz, 2H).
306	isoxazole- 5- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(isoxazole-5-
			carbonyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 419.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.73 (s,
			1H), 7.36 (d, J = 8.1 Hz, 2H), 7.25 (d, J =
			8.1 Hz, 2H), 6.88 (d, J = 1.7 Hz, 1H), 6.30
			(d, J = 6.4 Hz, 1H), 5.93 (t, J = 5.7 Hz,
			1H), 4.40 (d, J = 13.3 Hz, 1H), 4.17 (d, J =
			5.9 Hz, 2H), 3.73 (d, J = 13.6 Hz, 1H),
			3.16-3.08 (m, 1H), 3.00 (q, J = 6.5 Hz,
			2H), 2.81 (t, J = 12.6 Hz, 1H), 1.73 (dd, J =
			25.4, 13.4 Hz, 2H), 1.52 (dd, J = 14.6,
			7.2 Hz, 1H), 1.41-1.32 (m, 2H), 1.24 (s,
			4H), 1.09 (d, J = 13.7 Hz, 2H).
309	6- methylnico- tinic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(6-
			methylnicotinoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 443.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 8.45 (s, 1H), 7.69 (d, J = 8.0 Hz, 1H),
			7.35 (dt, J = 14.8, 5.6 Hz, 2H), 7.25 (t, J =
			4.4 Hz, 2H), 6.31 (s, 1H), 5.93 (s, 1H),
			4.45 (s, 1H), 4.18 (d, J = 5.9 Hz, 2H), 3.53
			(s, 1H), 3.33 (s, 2H), 3.01 (p, J = 7.3, 5.4
			Hz, 4H), 2.74 (s, 1H), 1.73 (q, J = 4.9 Hz,
			3H), 1.54 (d, J = 50.0 Hz, 2H), 1.30 (d, J =
			46.8 Hz, 5H), 1.06 (s, 2H).
310	2-(2- methylpyri- din-3- yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(2-
			methylpyridin-3-yl)acetyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 457.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 8.29 (d, J = 4.8 Hz, 1H), 8.15 (s, 1H),
			7.43 (d, J = 7.6 Hz, 2H), 7.36 (d, J = 8.1
			Hz, 2H), 7.26 (d, J = 8.1 Hz, 2H), 7.14
			(dd, J = 7.6, 4.9 Hz, 1H), 6.32 (t, J = 6.2
			Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H), 4.38 (d,
			J = 12.9 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H),
			3.94 (d, J = 13.6 Hz, 1H), 3.72 (d, J = 2.1
			Hz, 2H), 3.00 (q, J = 5.9 Hz, 3H), 2.36 (s,
			3H), 1.67 (d, J = 13.0 Hz, 2H), 1.47 (d, J =
			12.2 Hz, 1H), 1.36 (p, J = 6.9 Hz, 2H),
			1.25 (dq, J = 25.9, 8.0, 7.1 Hz, 4H), 1.08-
			0.85 (m, 2H).
311	2-(6- methylpyri- din-3- yl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(6-
			methylpyridin-3-yl)acetyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 457.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 8.27 (s, 1H), 7.49 (dd, J = 7.7, 2.2 Hz,
			1H), 7.36 (d, J = 8.1 Hz, 2H), 7.26 (d, J =
			8.1 Hz, 2H), 7.18 (d, J = 7.9 Hz, 1H), 6.31
			(t, J = 6.2 Hz, 1H), 5.93 (t, J = 5.8 Hz,
			1H), 4.36 (d, J = 13.1 Hz, 1H), 4.17 (d, J =
			6.0 Hz, 2H), 3.95 (d, J = 13.5 Hz, 1H),
			3.68 (s, 2H), 3.04-2.91 (m, 3H), 2.57 (d,
			J = 15.4 Hz, 1H), 2.43 (s, 3H), 1.68-1.59
			(m, 2H), 1.48-1.40 (m, 1H), 1.35 (p, J =
			6.9 Hz, 2H), 1.25 (q, J = 8.1, 7.3 Hz, 2H),
			1.18 (h, J = 6.3, 5.3 Hz, 2H), 0.92 (tt, J =
			12.0, 6.6 Hz, 2H).
312	1-methyl- 1H-1,2,3- triazole-4- carboxylic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(1-methyl-
			1H-1,2,3-triazole-4-carbonyl)piperidin-
			4-yl)butyl)urea. LRMS (APCI) m/z
			433.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.43 (s, 1H), 7.36 (d, J = 8.0
			Hz, 2H), 7.26 (d, J = 8.1 Hz, 2H), 6.32 (s,
			1H), 5.94 (s, 1H), 4.72 (d, J = 13.1 Hz,
			1H), 4.46 (d, J = 12.7 Hz, 1H), 4.17 (d, J =
			5.3 Hz, 2H), 4.08 (s, 3H), 3.11 (s, 1H),
			3.00 (q, J = 6.2 Hz, 2H), 2.72 (t, J = 13.1
			Hz, 1H), 1.78-1.63 (m, 2H), 1.52 (dt, J =
			11.0, 5.4 Hz, 1H), 1.36 (q, J = 6.8 Hz,
			2H), 1.26 (q, J = 8.8, 6.1 Hz, 4H), 1.15-
			0.95 (m, 2H).
313	2-(o- tolyl)acetic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-(o-
			tolyl)acetyl)piperidin-4-yl)butyl)urea.
			LRMS (APCI) m/z 456.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.36 (d, J =
			8.0 Hz, 2H), 7.26 (d, J = 8.0 Hz, 2H),
			7.13 (tt, J = 9.0, 5.2 Hz, 3H), 7.08-6.98
			(m, 1H), 6.31 (t, J = 6.4 Hz, 1H), 5.93 (t, J =
			5.7 Hz, 1H), 4.40 (d, J = 13.0 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.87 (d, J = 13.8
			Hz, 1H), 3.65 (d, J = 2.8 Hz, 2H), 3.17 (d,
			J = 5.2 Hz, 1H), 3.04-2.90 (m, 3H), 2.54
			(t, J = 12.7 Hz, 1H), 2.18 (s, 3H), 1.70-
			1.58 (m, 2H), 1.34 (q, J = 6.8 Hz, 2H),
			1.23 (dq, J = 28.5, 7.8, 7.0 Hz, 4H), 1.04-
			0.85 (m, 2H).
314	2- difluorometh- yl)benzo- ic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2-
			(difluoromethyl)benzoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 478.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.65 (dd, J = 26.4, 7.2 Hz, 1H), 7.58 (d,
			J = 6.3 Hz, 2H), 7.41-7.31 (m, 3H), 7.25
			(d, J = 8.1 Hz, 2H), 6.95 (t, J = 55.1 Hz,
			1H), 6.31 (t, J = 6.2 Hz, 1H), 5.93 (t, J =
			5.7 Hz, 1H), 4.50 (d, J = 12.9 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.27 (d, J = 13.5
			Hz, 2H), 3.18 (d, J = 5.2 Hz, 1H), 2.99 (q,
			J = 6.5 Hz, 2H), 2.82-2.70 (m, 1H), 1.74
			(d, J = 12.8 Hz, 1H), 1.57-1.44 (m, 2H),
			1.35 (q, J = 6.9 Hz, 2H), 1.31-1.16 (m,
			4H), 1.09 (d, J = 13.0 Hz, 1H).
315	2-(1H- tetrazol-5- yl)benzoic acid	3.8
			1-(4-(1-(2-(1H-tetrazol-5-
			yl)benzoyl)piperidin-4-yl)butyl)-3-(4-
			chlorobenzyl)urea. LRMS (APCI) m/z
			496.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.86 (s, 1H), 7.66-7.59 (m,
			2H), 7.43 (d, J = 6.5 Hz, 1H), 7.35 (d, J =
			8.0 Hz, 2H), 7.25 (d, J = 8.1 Hz, 2H), 6.31
			(t, J = 6.0 Hz, 1H), 5.93 (t, J = 5.5 Hz,
			1H), 4.44 (d, J = 12.9 Hz, 1H), 4.17 (d, J =
			5.9 Hz, 2H), 3.27 (dd, J = 6.6, 3.4 Hz,
			2H), 2.99 (q, J = 6.5 Hz, 2H), 2.65 (d, J =
			15.0 Hz, 1H), 1.81-1.56 (m, 2H), 1.42
			(s, 2H), 1.34 (d, J = 7.9 Hz, 2H), 1.22 (s,
			4H), 1.07 (d, J = 12.5 Hz, 2H).
316	2-(1H- pyrazol-4- yl)acetic acid	3.8
			1-(4-(1-(2-(1H-pyrazol-4-
			yl)acetyl)piperidin-4-yl)butyl)-3-(4-
			chlorobenzyl)urea. LRMS (APCI) m/z
			432.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.43 (s, 2H), 7.36 (d, J = 8.0
			Hz, 2H), 7.25 (d, J = 8.0 Hz, 2H), 6.31 (t,
			J = 6.1 Hz, 1H), 5.93 (t, J = 5.7 Hz, 1H),
			4.36 (d, J = 13.0 Hz, 1H), 4.17 (d, J = 6.0
			Hz, 2H), 4.10 (s, 1H), 3.91 (d, J = 13.5
			Hz, 1H), 3.50 (s, 2H), 3.17 (s, 2H), 3.04-
			2.87 (m, 3H), 1.60 (d, J = 11.0 Hz, 2H),
			1.34 (p, J = 6.9 Hz, 2H), 1.23 (dq, J =
			10.4, 5.8, 5.3 Hz, 2H), 1.16 (q, J = 7.0 Hz,
			2H), 0.87 (q, J = 12.4 Hz, 2H).
317	benzoic acid	3.9
			1-(4-(4-benzoylpiperazin-1-yl)butyl)-3-
			(4-chlorobenzyl)urea. LRMS (APCI)
			m/z 429.2 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.46 (d, J = 5.2 Hz, 3H),
			7.42-7.32 (m, 4H), 7.25 (d, J = 8.0 Hz,
			2H), 6.35 (t, J = 6.1 Hz, 1H), 5.98 (t, J =
			6.0 Hz, 1H),
			4.17 (d, J = 6.0 Hz, 2H), 3.50-3.25 (m,
			7H), 3.17 (s, 1H), 3.01 (q, J = 6.4 Hz,
			2H), 2.48-2.36 (m, 2H), 1.42 (dq, J =
			21.1, 8.0, 7.3 Hz, 4H).
319	2,6- dimethylben- zoic acid	3.8
			1-(4-chlorobenzyl)-3-(4-(1-(2,6-
			dimethylbenzoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 456.2
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 8.14 (s, 1H), 7.35 (d, J = 8.1 Hz, 2H),
			7.25 (d, J = 8.1 Hz, 2H), 7.16 (t, J = 7.5
			Hz, 1H), 7.06 (t, J = 6.5 Hz, 2H), 6.31 (t,
			J = 6.2 Hz, 1H), 5.92 (t, J = 5.7 Hz, 1H),
			4.57 (d, J = 13.1 Hz, 1H), 4.17 (d, J = 6.0
			Hz, 2H), 4.03 (q, J = 7.1 Hz, 1H), 3.17 (d,
			J = 13.3 Hz, 1H), 3.04-2.91 (m, 3H),
			2.73 (td, J = 12.7, 2.8 Hz, 1H), 2.14 (d, J =
			30.5 Hz, 6H), 1.81-1.73 (m, 1H), 1.56
			(d, J = 13.3 Hz, 1H), 1.35 (t, J = 7.0 Hz,
			2H), 1.24 (dt, J = 9.4, 4.3 Hz, 3H), 0.96
			(dqd, J = 48.4, 12.3, 4.3 Hz, 2H).
320	2- methylbenzo- ic acid	3.10
			1-(4-(1-(2-methylbenzoyl)piperidin-4-
			yl)butyl)-3-(oxazol-5-ylmethyl)urea.
			LRMS (APCI) m/z 399.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.26 (tt, J =
			15.2, 7.3 Hz, 4H), 7.12 (dd, J = 21.1,
			7.5 Hz, 1H), 6.92 (s, 1H), 6.27 (t, J = 5.9
			Hz, 1H), 5.94 (t, J = 5.7 Hz, 1H), 4.52 (d,
			J = 13.0 Hz, 1H), 4.24 (d, J = 5.8 Hz, 2H),
			3.05-2.87 (m, 4H), 2.72 (t, J = 12.7 Hz,
			1H), 2.20 (d, J = 20.9 Hz, 3H), 1.78-
			1.68 (m, 1H), 1.49 (dd, J = 29.9, 14.9 Hz,
			3H), 1.34 (q, J = 6.8 Hz, 2H), 1.23 (d, J =
			7.5 Hz, 5H).
321	2- methylbenzo ic acid	3.12
			4-((3-(4-(1-(2-methylbenzoyl)piperidin-
			4-yl)butyl)ureido)methyl)benzamide.
			LRMS (APCI) m/z 451.3 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.90 (s,
			1H), 7.81 (d, J = 8.0 Hz, 2H), 7.38-7.18
			(m, 5H), 7.13 (d, J = 18.6 Hz, 1H), 6.32 (t,
			J = 6.2 Hz, 1H), 5.94 (t, J = 5.8 Hz, 1H),
			4.52 (d, J = 13.1 Hz, 1H), 4.23 (d, J = 6.0
			Hz, 2H), 3.07-2.99 (m, 2H), 2.99-2.88
			(m, 2H), 2.73 (t, J = 12.2 Hz, 1H), 2.20 (d,
			J = 19.9 Hz, 3H), 1.74 (q, J = 5.4, 3.1 Hz,
			2H), 1.51 (d, J = 34.1 Hz, 2H), 1.35 (d, J =
			7.1 Hz, 2H), 1.24 (s, 4H), 1.11-0.92
			(m, 2H).
322	2- methylbenzo- ic acid	3.11
			1-(4-methoxybenzyl)-3-(4-(1-(2-
			methylbenzoyl)piperidin-4-
			yl)butyl)urea. LRMS (APCI) m/z 438.3
			(M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.26 (tt, J = 15.4, 7.3 Hz, 3H), 7.15 (d, J =
			8.2 Hz, 2H), 7.09 (d, J = 7.7 Hz, 1H),
			6.85 (d, J = 8.2 Hz, 2H), 6.16 (t, J = 6.0
			Hz, 1H), 5.83 (t, J = 5.7 Hz, 1H), 4.52 (d,
			J = 12.9 Hz, 1H), 4.11 (d, J = 5.9 Hz, 2H),
			3.72 (s, 3H), 3.04-2.87 (m, 3H), 2.72 (t,
			J = 12.5 Hz, 1H), 2.20 (d, J = 20.2 Hz,
			3H), 1.75 (d, J = 13.0 Hz, 1H), 1.64-
			1.40 (m, 2H), 1.35 (t, J = 7.0 Hz, 2H),
			1.21 (dq, J = 14.3, 6.9 Hz, 5H), 1.00 (dt, J =
			41.7, 12.9 Hz, 2H).
323	2- methylbenzo- ic acid	3.13
			1-(4-(1-(2-methylbenzoyl)piperidin-4-
			yl)butyl)-3-(pyridin-4-ylmethyl)urea.
			LRMS (APCI) m/z 409.2 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.47 (s,
			2H), 7.25 (dt, J = 22.2, 6.3 Hz, 5H), 7.18-
			7.08 (m, 1H), 6.42 (t, J = 6.2 Hz, 1H),
			6.05 (t, J = 5.7 Hz, 1H), 4.52 (d, J = 13.1
			Hz, 1H), 4.21 (d, J = 6.1 Hz, 2H), 3.05-
			2.87 (m, 3H), 2.73 (dd, J = 14.5, 10.8 Hz,
			1H), 2.20 (d, J = 20.1 Hz, 3H), 1.75 (d, J =
			12.9 Hz, 1H), 1.66-1.41 (m, 3H), 1.36
			(q, J = 7.0 Hz, 2H), 1.25 (d, J = 10.8 Hz,
			4H), 1.10-0.86 (m, 2H).
293	Benzoic acid	3.15
			1-(4-(1-benzoylpiperidin-4-yl)butyl-1,1-
			d2)-3-(oxazol-5-ylmethyl)urea. LRMS
			(APCI) m/z 387 (M + H). 1H NMR (300
			MHz, DMSO) δ 1.07 (s, 2H), 1.21-2.12
			(m, 9H), 2.86 (d, J = 69.7 Hz, 2H), 3.55
			(s, 1H), 4.26 (dd, J = 5.9, 1.0 Hz, 2H),
			4.46 (s, 1H), 5.93 (s, 1H), 6.27 (t, J = 5.9
			Hz, 1H), 6.93 (d, J = 0.9 Hz, 1H), 7.33-
			7.49 (m, 5H), 8.26 (s, 1H).

Example 2

Preparation of N-benzyl-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide (Compound 68)

Preparation of N-benzyl-6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxamide.

HATU (201 mg, 0.529 mmol, 2 equiv) was added to a stirring solution of 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (80 mg, 0.265 mmol, 1.5 equiv), phenylmethanamide (57 mg, 0.529 mmol, 2 equiv) and NEt₃ (134 mg, 1.32 mmol, 5 equiv) in DMF (0.5 mL) at rt. After 3 h, the reaction was quenched with saturated ammonium chloride, extracted with CH₂Cl₂, organics combined, dried over sodium sulfate, filtered, and product was isolated by reverse phase HPLC (10->100% MeCN/H2O w/0.1% formic acid) as a white solid (10 mg, 9%). LRMS (APCI) m/z 408 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.18 (t, J=6.0 Hz, 1H), 7.31 (t, J=7.4 Hz, 2H), 7.21 (d, J=7.7 Hz, 3H), 7.15 (d, J=8.1 Hz, 2H), 6.87 (d, J=8.0 Hz, 2H), 6.20-5.97 (m, 2H), 4.24 (d, J=5.8 Hz, 2H), 4.10 (d, J=5.7 Hz, 2H), 3.92 (h, J=8.2 Hz, 1H), 3.72 (s, 3H), 2.93 (p, J=8.4 Hz, 1H), 2.35 (dt, J=11.9, 6.2 Hz, 1H), 2.15 (p, J=10.1 Hz, 4H), 2.05-1.88 (m, 1H), 1.80 (t, J=9.7 Hz, 1H), 1.71 (t, J=9.9 Hz, 1H).

Compounds in the following table were prepared in a similar manner as Compound 68, using the intermediates and reagents as listed.

Compound No.	Amine	Intermediate	Structure, Name and Data
43	1- phenylcyclo- propan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(1-
			phenylcyclopropyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 434 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.38 (s, 1H), 7.25
			(t, J = 7.6 Hz, 2H), 7.20-7.02 (m, 5H), 6.87 (d, J =
			8.4 Hz, 2H), 6.20-5.98 (m, 2H), 4.10 (d, J =
			5.4 Hz, 2H), 3.92 (q, J = 8.0 Hz, 1H), 3.72 (s, 3H),
			2.91 (p, J = 8.5 Hz, 1H), 2.35 (ddd, J = 11.4, 7.2,
			5.2 Hz, 1H), 2.11 (dd, J = 19.9, 8.4 Hz, 4H), 2.04-
			1.89 (m, 1H), 1.79 (dd, J = 10.6, 8.7 Hz, 1H),
			1.70 (dd, J = 11.1, 8.8 Hz, 1H), 1.13 (t, J = 3.0 Hz,
			2H), 1.11-1.00 (m, 2H).
45	(R)-1- phenylethan- 1-amine	2.2
			(R)-6-(3-(4-methoxybenzyl)ureido)-N-(1-
			phenylethyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 422 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.09 (d, J = 8.2 Hz, 1H), 7.29
			(dt, J = 13.5, 4.7 Hz, 4H), 7.21 (t, J = 7.1 Hz, 1H),
			7.15 (d, J = 8.3 Hz, 2H), 6.86 (d, J = 8.3 Hz, 2H),
			6.17-6.00 (m, 2H), 4.89 (p, J = 7.3 Hz, 1H), 4.10
			(d, J = 5.9 Hz, 2H), 3.91 (hd, J = 8.1, 3.9 Hz, 1H),
			3.733 (s, 3H), 2.93 (p, J = 8.5 Hz, 1H), 2.34 (dt, J =
			11.7, 6.1 Hz, 1H), 2.21-2.00 (m, 4H), 1.93 (dtt,
			J = 8.3, 5.2, 2.5 Hz, 1H), 1.86-1.73 (m, 1H), 1.68
			(ddd, J = 11.5, 8.8, 3.0 Hz, 1H), 1.31 (d, J = 6.9
			Hz, 3H).
47	(S)-1- phenylethan- 1-amine	2.2
			(S)-6-(3-(4-methoxybenzyl)ureido)-N-(1-
			phenylethyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 422 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.09 (d, J = 8.1 Hz, 1H), 7.41-
			7.18 (m, 5H), 7.15 (d, J = 8.3 Hz, 2H), 6.86 (d, J =
			8.3 Hz, 2H)), 6.21-5.98 (m, 2H), 4.88 (p, J = 7.3
			Hz, 1H), 4.09 (d, J = 5.9 Hz, 2H), 3.91 (qd, J =
			8.0, 4.2 Hz, 1H), 3.72 (s, 3H), 2.92 (p, J = 8.5 Hz,
			1H), 2.34 (dt, J = 11.5, 6.0 Hz, 1H), 2.20-2.01
			(m, 4H), 1.93 (ddp, J = 11.4, 8.3, 4.2, 3.7 Hz, 1H),
			1.86-1.74 (m, 1H), 1.68 (ddd, J = 11.5, 8.7, 3.0
			Hz, 1H), 1.41-1.12 (m, 3H).
44	2- phenylpyrrolidine	2.2
			1-(4-methoxybenzyl)-3-(6-(2-phenylpyrrolidine-
			1-carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 448 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.35 (td, J = 7.4, 4.9 Hz, 1H), 7.28
			(qd, J = 7.5, 2.3 Hz, 3H), 7.23-7.05 (m, 3H), 6.86
			(dd, J = 8.5, 6.2 Hz, 2H), 6.24-6.04 (m, 1H), 6.05-
			5.94 (m, 1H), 5.10-4.79 (m, 1H), 4.10 (d, J =
			5.9 Hz, 1H), 4.06 (d, J = 5.9 Hz, 1H), 3.92 (ddp, J =
			11.5, 7.8, 4.1, 3.5 Hz, 1H), 3.72 (d, J = 3.0 Hz,
			3H), 3.65-3.45 (m, 2H), 3.28-3.15 (m, 1H),
			2.75 (p, J = 8.7 Hz, 1H), 2.40 (p, J = 6.2 Hz, 1H),
			2.24-1.96 (m, 2H), 1.91-1.51 (m, 6H), 1.19
			(dddd, J = 35.6, 11.6, 8.2, 3.7 Hz, 2H).
46	(S)- amino- 2- phenylethan- 1-ol	2.2
			(S)-N-(2-hydroxy-1-phenylethyl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 422 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.03 (dd, J =
			8.3, 3.2 Hz, 1H), 7.34-7.25 (m, 4H), 7.25-7.19
			(m, 1H), 7.15 (d, J = 8.3 Hz, 2H), 6.86 (d, J = 8.4
			Hz, 2H), 6.22-5.97 (m, 2H), 4.81 (q, J = 7.6, 7.1
			Hz, 2H), 4.09 (d, J = 5.9 Hz, 2H), 3.91 (qd, J =
			8.3, 5.9 Hz, 1H), 3.72 (s, 3H), 3.52 (d, J = 6.4 Hz,
			2H), 2.98 (p, J = 8.4 Hz, 1H), 2.35 (ddd, J = 13.6,
			7.6, 3.7 Hz, 1H), 2.10 (tdd, J = 22.9, 10.6, 7.5 Hz,
			4H), 1.95 (dtd, J = 10.8, 5.2, 2.7 Hz, 1H), 1.79
			(ddd, J = 11.4, 8.9, 3.2 Hz, 1H), 1.68 (ddd, J =
			11.8, 8.8, 3.9 Hz, 1H).
48	2- phenylazetidine	2.2
			1-(4-methoxybenzyl)-3-(6-(2-phenylazetidine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434 (M + H). 1H NMR (400 MHz,
			DMSO-d6); δ 8.32 (s, 1H), 7.64 (t, J = 5.5 Hz,
			1H), 7.41 (d, J = 3.5 Hz, 1H), 7.31 (d, J = 4.6 Hz,
			2H), 7.22 (p, J = 4.3 Hz, 1H), 7.15 (d, J = 8.4 Hz,
			2H), 6.86 (d, J = 8.3 Hz, 1H), 6.22-6.08 (m, 1H),
			6.04 (t, J = 8.3 Hz, 1H), 5.19 (t, J = 7.7 Hz, 1H),
			4.53 (t, J = 6.5 Hz, 1H), 4.08 (dd, J = 11.9, 5.7 Hz,
			1H), 3.91 (q, J = 8.0 Hz, 1H), 3.72 (s, 3H), 3.16-
			2.99 (m, 2H), 2.83 (p, J = 8.4 Hz, 1H), 2.65 (dt, J =
			15.7, 8.0 Hz, 1H), 2.43-2.27 (m, 1H), 2.20-
			2.04 (m, 2H), 2.01 (dd, J = 9.5, 4.9 Hz, 1H), 1.95-
			1.86 (m, 1H), 1.78 (t, J = 9.8 Hz, 1H), 1.73-
			1.64 (m, 2H), 1.28-1.09 (m, 1H).
49	pyridin- 3- ylmethanamine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-3-
			ylmethyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 409 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.45 (d, J = 3.4 Hz, 2H), 8.25
			(t, J = 6.0 Hz, 1H), 7.62 (dd, J = 7.8, 2.1 Hz, 2H),
			7.35 (dd, J = 7.8, 4.7 Hz, 1H), 7.15 (d, J = 8.3 Hz,
			2H), 6.86 (d, J = 8.3 Hz, 2H), 6.21-5.95 (m, 1H),
			4.26 (d, J = 5.8 Hz, 2H), 4.09 (d, J = 5.9 Hz, 2H),
			3.91 (q, J = 8.0 Hz, 1H), 3.72 (s, 3H), 2.92 (p, J =
			8.5 Hz, 1H), 2.34 (ddd, J = 11.8, 7.3, 5.2 Hz, 1H),
			2.13 (dq, J = 11.4, 8.3 Hz, 4H), 1.96 (ddd, J =
			11.3, 8.2, 2.6 Hz, 1H), 1.79 (dd, J = 10.6, 8.7 Hz,
			1H), 1.70 (dd, J = 11.1, 8.8 Hz, 1H).
50	pyridin- 4- ylmethanamine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-4-
			ylmethyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 409 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.49 (d, J = 4.9 Hz, 2H), 8.29
			(t, J = 6.1 Hz, 1H), 7.21 (d, J = 5.0 Hz, 2H), 7.15
			(d, J = 8.3 Hz, 2H), 6.87 (d, J = 8.4 Hz, 2H), 6.27-
			5.84 (m, 2H), 4.26 (d, J = 6.0 Hz, 2H), 4.09 (d, J =
			5.9 Hz, 2H), 3.92 (q, J = 8.0 Hz, 1H), 3.72 (s,
			3H), 2.96 (p, J = 8.5 Hz, 1H), 8.36 (ddd, J = 11.9,
			7.2, 5.1 Hz, 1H), 2.16-2.07 (m, 4H), 1.99 (ddd, J =
			11.1, 8.4, 2.2 Hz, 1H), 1.80 (dd, J = 10.6, 8.7
			Hz, 1H), 1.71 (dd, J = 11.0, 8.8 Hz, 1H).
51	N- methyl- 1- phenylmethanamine	2.2
			N-benzyl-6-(3-(4-methoxybenzyl)ureido)-N-
			methylspiro[3.3]heptane-2-carboxamide. LRMS
			(APCI) m/z 422 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.35 (dt, J = 17.2, 7.4 Hz, 2H), 7.26
			(q, J = 7.3, 6.6 Hz, 1H), 7.21-7.06 (m, 4H), 6.86
			(dd, J = 8.7, 3.4 Hz, 2H), 6.10 (dq, J = 14.0, 8.0,
			7.0 Hz, 2H), 4.47 (d, J = 2.1 Hz, 2H), 4.09 (t, J =
			5.9 Hz, 1H), 4.01-3.80 (m, 1H), 3.72 (s, 3H),
			3.26 (dt, J = 13.6, 8.5 Hz, 1H), 2.80 (s, 2H), 2.75
			(s, 1H), 2.39 (ddd, J = 11.6, 7.3, 5.3 Hz, 1H), 2.35-
			2.29 (m, 1H), 2.29-2.02 (m, 5H), 1.87-1.77
			(m, 1H), 1.71 (ddt, J = 14.5, 11.1, 5.9 Hz, 1H).
53	(R)-1- (2- fluorophenyl) ethan-1-amine	2.2
			(R)-N-(1-(2-fluorophenyl)ethyl)-6-(3-(4-
			methoxybenzyl)ureido)-N-
			methylspiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 454 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.39 (ddq, J = 21.0, 13.8, 7.3,
			6.8 Hz, 2H), 7.26-7.09 (m, 4H), 6.86 (d, J = 8.4
			Hz, 2H), 6.21-6.03 (m, 2H), 5.88 (q, J = 7.1 Hz,
			1H), 4.09 (d, J = 5.9 Hz, 2H), 3.91 (p, J = 7.9, 6.8
			Hz, 1H), 3.72 (s, 3H), 3.30-3.25 (m, 2H), 3.18
			(p, J = 8.5 Hz, 1H), 2.55-2.46 (m, 3H), 2.46-
			2.28 (m, 1H), 2.29-1.96 (m, 3H), 1.90-1.62 (m,
			3H), 1.49 (dd, J = 6.9, 3.9 Hz, 1H), 1.38 (d, J = 7.0
			Hz, 2H).
54	2- methyl- 2-(o-tolyl) propan-1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-
			(o-tolyl)propyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 464 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.39 (ddq, J = 21.0,
			13.8, 7.3, 6.8 Hz, 2H), 7.26-7.09 (m, 4H), 6.86
			(d, J = 8.4 Hz, 2H), 6.21-6.03 (m, 2H), 5.88 (q, J =
			7.1 Hz, 1H), 4.09 (d, J = 5.9 Hz, 2H), 3.91 (p, J =
			7.9, 6.8 Hz, 1H), 3.72 (s, 3H), 3.18 (p, J = 8.5
			Hz, 1H), 2.55-2.46 (m, 3H), 2.46-2.28 (m, 1H),
			2.29-1.96 (m, 4H), 1.90-1.62 (m, 2H), 1.49 (dd,
			J = 6.9, 3.9 Hz, 1H), 1.38 (d, J = 7.0 Hz, 2H), 1.21
			(d, J = 2.2 Hz, 6H).
55	2-(2- fluorophenyl)- 2-methylpropan- 1-amine	2.2
			N-(2-(2-fluorophenyl)-2-methylpropyl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 468 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.45 (t, J = 6.3
			Hz, 1H), 7.25 (dd, J = 7.0, 3.1 Hz, 1H), 7.20-
			7.03 (m, 5H), 6.86 (d, J = 8.5 Hz, 2H), 6.17-5.99
			(m, 2H), 4.09 (d, J = 4.9 Hz, 2H), 3.88 (q, J = 7.6
			Hz, 1H), 3.72 (s, 3H), 2.87 (p, J = 8.4 Hz, 1H),
			2.37-2.24 (m, 3H), 2.11 (ddd, J = 12.0, 7.3, 5.2
			Hz, 1H), 1.86 (t, J = 9.8 Hz, 1H), 1.80-1.72 (m,
			4H), 1.66 (dd, J = 11.0, 8.8 Hz, 1H), 1.29 (d, J =
			7.9 Hz, 6H).
56	pyridin- 2- ylmethanamine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(pyridin-2-
			ylmethyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 409 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.49 (d, J = 4.8 Hz, 1H), 8.27
			(t, J = 6.0 Hz, 1H), 7.77 (t, J = 7.8 Hz, 1H), 7.34-
			7.21 (m, 2H), 7.19-7.04 (m, 2H), 6.87 (dd, J =
			8.5, 1.9 Hz, 2H), 6.21-5.94 (m, 2H), 4.34 (d, J =
			5.8 Hz, 2H), 4.10 (d, J = 5.6 Hz, 2H), 3.91 (dt, J =
			15.0, 7.6 Hz, 1H), 3.72 (d, J = 1.7 Hz, 3H), 2.98
			(p, J = 8.4 Hz, 1H), 2.36 (dt, J = 11.6, 6.2 Hz, 1H),
			2.25-2.07 (m, 4H), 2.07-1.93 (m, 1H), 1.80 (t, J =
			9.7 Hz, 1H), 1.71 (t, J = 9.9 Hz, 1H).
57	3-phenyl- pyrrolidine	2.2
			1-(4-methoxybenzyl)-3-(6-(3-phenylpyrrolidine-
			1-carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 448 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.38-7.27 (m, 4H), 7.27-7.19 (m,
			1H), 7.15 (dt, J = 8.7, 2.2 Hz, 2H), 6.86 (dt, J =
			8.5, 2.3 Hz, 2H), 6.11 (p, J = 6.9, 6.4 Hz, 2H),
			4.09 (d, J = 5.0 Hz, 2H), 3.92 (p, J = 7.8 Hz, 1H),
			3.79 (t, J = 7.0 Hz, 1H), 3.72 (s, 3H), 3.55 (q, J =
			8.7, 8.0 Hz, 1H), 3.33-3.29 (m, 2H), 3.28 (dt, J =
			10.3, 5.1 Hz, 1H), 3.22-3.08 (m, 2H), 2.37 (dq, J =
			11.1, 6.3, 5.8 Hz, 1H), 2.16 (dt, J = 19.7, 9.7 Hz,
			4H), 1.96 (dq, J = 45.5, 10.6 Hz, 2H), 1.80 (q, J =
			10.4 Hz, 1H), 1.70 (dt, J = 10.7, 7.8 Hz, 1H).
58	4- (pyrrolidin- 2-yl)pyridine	2.2
			1-(4-methoxybenzyl)-3-(6-(2-(pyridin-4-
			yl)pyrrolidine-1-carbonyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 449 (M + H). 1H
			NMR (400 MHz, DMSO-d6); ratio or rotamers
			4:1. δ 8.52 (s, 3H), 7.20 (d, J = 4.9 Hz, 2H), 7.15
			(d, J = 8.2 Hz, 6H), 6.94-6.67 (m, 4H), 6.11 (dd,
			J = 12.3, 6.9 Hz, 3H), 6.23 (t, J = 8.9 Hz, 1H), 6.01
			(t, J = 8.9 Hz, 1H), 5.01 (d, J = 8.0 Hz, 1H), 4.98-
			4.85 (m, 1H), 4.08 (dd, J = 12.5, 5.8 Hz, 4H), 3.91
			(tt, J = 18.1, 7.9 Hz, 2H), 3.72 (s, 6H), 3.68-3.56
			(m, 2H), 3.50 (q, J = 9.0, 8.2 Hz, 1H), 3.24 (p, J =
			8.8 Hz, 4H), 2.74 (hept, J = 8.2 Hz, 1H), 2.66 (p, J =
			8.8 Hz, 2H), 2.61 (hept, J = 8.2 Hz, 1H), 2.45-
			2.37 (m, 4H), 2.36-2.26 (m, 1H), 2.22 (d, J =
			20.0 Hz, 1H), 1.95-1.62 (m, 9H), 1.62-1.50 (m,
			2H), 1.40-1.27 (m, 1H), 1.22 (t, J = 9.9 Hz, 1H).
59	(R)-3- (pyrrolidin- 2-yl)pyridine	2.2
			(R)-1-(4-methoxybenzyl)-3-(6-(2-(pyridin-3-
			yl)pyrrolidine-1-carbonyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 449 (M + H). 1H NMR
			(400 MHz, DMSO-d6); ratio or rotamers 4:1. δ
			8.60-8.25 (m, 3H), 7.58 (d, J = 8.0 Hz, 1H), 7.52
			(d, J = 7.9 Hz, 1H), 7.38 (d, J = 6.5 Hz, 1H), 7.32
			(dd, J = 8.1, 4.0 Hz, 1H), 7.14 (t, J = 8.8 Hz, 5H),
			6.93-6.75 (m, 5H), 6.10 (dd, J = 12.6, 6.8 Hz,
			2H), 6.00 (dd, J = 11.2, 8.2 Hz, 1H), 5.06 (d, J =
			7.9 Hz, 1H), 5.00 (d, J = 8.0 Hz, 1H), 4.08 (dd, J =
			11.8, 5.8 Hz, 4H), 3.99-3.80 (m, 4H), 3.72 (s,
			6H), 3.63 (ddq, J = 13.8, 10.2, 4.6 Hz, 1H), 3.50
			(q, J = 9.0 Hz, 1H), 3.30-3.29 (m, 5H), 3.23 (p, J =
			9.0 Hz, 1H), 2.79 (q, J = 8.5 Hz, 1H), 2.38 (dd, J =
			11.5, 6.2 Hz, 1H), 2.32-1.97 (m, 8H), 1.95-
			1.74 (m, 5H), 1.69 (q, J = 11.6, 8.7 Hz, 2H), 1.57
			(t, J = 11.2 Hz, 1H), 1.31-1.19 (m, 1H), 1.19-
			1.04 (m, 1H).
60	(S)-1-(2- fluorophenyl)- N- methylethan- 1-amine	2.2
			(S)-N-(1-(2-fluorophenyl)ethyl)-6-(3-(4-
			methoxybenzyl)ureido)-N-
			methylspiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 454 (M + H). 1H NMR (400
			MHz, DMSO-d6); ratio of rotamers 2:1. δ 7.37 (tt,
			J = 13.8, 7.8 Hz, 4H), 7.15 (d, J = 8.1 Hz, 5H),
			6.86 (d, J = 8.0 Hz, 5H), 6.19-5.96 (m, 4H), 5.88
			(q, J = 7.2 Hz, 1H), 5.34-5.17 (m, 1H), 4.10 (d, J =
			5.7 Hz, 3H), 3.92 (dd, J = 12.1, 6.3 Hz, 2H),
			3.72 (s, 6H), 3.18 (p, J = 8.5 Hz, 2H), 2.50 (d, J =
			7.9 Hz, 9H), 2.46-2.30 (m, 1H), 2.20 (d, J = 8.2
			Hz, 1H), 2.14 (q, J = 10.5, 9.4 Hz, 1H), 2.06 (dd, J =
			8.8, 5.1 Hz, 1H), 1.94 (d, J = 11.4 Hz, 1H), 1.81
			(q, J = 9.7, 8.5 Hz, 4H), 1.70 (td, J = 10.2, 4.4 Hz,
			4H), 1.49 (dd, J = 6.7, 3.9 Hz, 3H), 1.38 (d, J = 7.1
			Hz, 6H).
61	3- phenyl- azetidine	2.2
			1-(4-methoxybenzyl)-3-(6-(3-phenylazetidine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.39 (d, J = 7.5 Hz, 4H), 7.31 (d, J =
			7.0 Hz, 1H), 7.18 (d, J = 7.9 Hz, 2H), 6.90 (d, J =
			8.0 Hz, 2H), 6.24-6.05 (m, 2H), 4.46 (dt, J = 8.3,
			4.3 Hz, 1H), 4.33-4.21 (m, 1H), 4.13 (d, J = 5.5
			Hz, 2H), 4.05 (dt, J = 9.9, 5.5 Hz, 1H), 3.95 (q, J =
			8.0 Hz, 1H), 3.84 (q, J = 6.9 Hz, 2H), 3.76 (d, J =
			1.6 Hz, 3H), 3.21 (d, J = 1.5 Hz, 1H), 3.03 (p, J =
			8.5 Hz, 1H), 2.40 (dt, J = 11.7, 6.2 Hz, 1H), 2.29-
			2.08 (m, 3H), 2.03 (t, J = 10.2 Hz, 1H), 1.83 (t, J =
			9.7 Hz, 1H), 1.74 (t, J = 10.0 Hz, 1H).
62	phenyl (piperazin)- 1-yl)methanone	2.2
			1-(6-(4-benzoylpiperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 491
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.56-
			7.43 (m, 3H), 7.41 (d, J = 5.3 Hz, 2H), 7.15 (d, J =
			8.0 Hz, 2H), 6.86 (d, J = 7.8 Hz, 2H), 6.10 (q, J =
			8.0, 7.0 Hz, 2H), 4.10 (t, J = 7.1 Hz, 6H), 3.91 (q,
			J = 8.1 Hz, 1H), 3.72 (s, 3H), 3.64-3.40 (m, 5H),
			2.37 (s, 1H), 2.27-2.08 (m, 4H), 2.03 (s, 1H),
			1.80 (t, J = 9.7 Hz, 1H), 1.70 (t, J = 9.9 Hz, 1H).
63	(1R,3R)- 3- phenyl- cyclobutan-1- amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-((1r,3r)-3-
			phenylcyclobutyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 448 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.10 (d, J = 7.1 Hz,
			1H), 7.30 (dt, J = 12.7, 7.6 Hz, 4H), 7.23-7.06
			(m, 3H), 6.95-6.70 (m, 2H), 6.19-5.89 (m, 2H),
			4.27 (q, J = 7.1 Hz, 1H), 4.10 (d, J = 5.8 Hz, 2H),
			3.92 (h, J = 8.2 Hz, 1H), 3.72 (d, J = 1.5 Hz, 3H),
			3.51 (p, J = 7.2 Hz, 1H), 2.86 (p, J = 8.3 Hz, 1H),
			2.33 (t, J = 6.3 Hz, 4H), 2.12 (ddd, J = 15.2, 11.8,
			7.4 Hz, 5H), 1.94 (td, J = 11.9, 6.2 Hz, 1H), 1.79
			(t, J = 9.7 Hz, 1H), 1.70 (t, J = 10.0 Hz, 1H).
64	2-(2- methoxy phenyl)- 2- methylpropan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-(2-
			methoxyphenyl)-2-
			methylpropyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 480 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.27-7.05 (m,
			5H), 6.97 (d, J = 8.3 Hz, 1H), 6.86 (d, J = 7.9 Hz,
			3H), 6.11 (t, J = 6.2 Hz, 1H), 6.06 (d, J = 8.1 Hz,
			1H), 4.09 (d, J = 5.6 Hz, 2H), 3.87 (p, J = 8.1 Hz,
			1H), 3.79 (s, 3H), 3.72 (s, 3H), 3.45 (d, J = 6.2 Hz,
			2H), 2.84 (p, J = 8.4 Hz, 1H), 2.29 (dt, J = 11.8,
			6.1 Hz, 1H), 2.11 (dt, J = 12.1, 6.2 Hz, 1H), 2.06-
			1.92 (m, 3H), 1.84 (t, J = 9.5 Hz, 1H), 1.74 (t, J =
			9.7 Hz, 1H), 1.65 (t, J = 9.9 Hz, 1H), 1.24 (s, 6H).
65	2- methyl- 2- (pyridin-2- yl)propan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-
			(pyridin-2-yl)propyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 451 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.52 (d, J = 4.8 Hz,
			1H), 7.72 (t, J = 7.8 Hz, 1H), 7.37 (d, J = 7.7 Hz,
			2H), 7.20 (t, J = 6.2 Hz, 1H), 7.14 (d, J = 8.2 Hz,
			2H), 6.86 (d, J = 7.9 Hz, 2H), 6.11 (t, J = 6.3 Hz,
			1H), 6.07 (d, J = 8.1 Hz, 1H), 4.09 (d, J = 6.0 Hz,
			3H), 3.89 (h, J = 8.2 Hz, 1H), 3.72 (s, 3H), 3.18 (d,
			J = 4.0 Hz, 1H), 2.88 (p, J = 8.4 Hz, 1H), 2.31 (dt,
			J = 11.7, 6.3 Hz, 1H), 2.12 (dt, J = 12.1, 6.3 Hz,
			1H), 2.03 (dd, J = 15.4, 8.8 Hz, 3H), 1.87 (t, J =
			9.8 Hz, 1H), 1.76 (t, J = 9.7 Hz, 1H), 1.67 (t, J =
			9.9 Hz, 1H), 1.23 (s, 6H).
66	2-methyl- 2- (pyridin-3- yl)propan-1- amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-
			(pyridin-3-yl)propyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 451 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.57 (s, 1H), 8.40
			(d, J = 4.5 Hz, 1H), 7.74 (d, J = 8.2 Hz, 1H), 7.48
			(t, J = 6.2 Hz, 1H), 7.37-7.26 (m, 1H), 7.14 (d, J =
			8.0 Hz, 3H), 6.86 (d, J = 8.0 Hz, 2H), 6.10 (t, J =
			6.0 Hz, 1H), 4.09 (d, J = 5.8 Hz, 2H), 3.88 (q, J =
			8.0 Hz, 1H), 3.72 (s, 3H), 2.83 (q, J = 8.4 Hz, 1H),
			2.36-2.20 (m, 2H), 2.10 (t, J = 8.8 Hz, 1H), 1.98
			(dd, J = 19.8, 9.0 Hz, 4H), 1.84 (t, J = 9.8 Hz, 1H),
			1.74 (t, J = 9.6 Hz, 1H), 1.65 (t, J = 10.0 Hz, 1H),
			1.25 (s, 6H).
69	2- phenylethan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-
			phenethylspiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 422 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 7.72 (t, J = 5.7 Hz, 1H), 7.27
			(d, J = 7.5 Hz, 2H), 7.24-7.09 (m, 5H), 6.94-
			6.68 (m, 2H), 6.20-5.92 (m, 2H), 4.10 (d, J = 5.8
			Hz, 2H), 3.91 (h, J = 8.1 Hz, 1H), 3.72 (d, J = 1.6
			Hz, 3H), 3.24 (q, J = 6.9 Hz, 2H), 2.82 (p, J = 8.4
			Hz, 1H), 2.68 (t, J = 7.5 Hz, 2H), 2.33 (dt, J =
			11.5, 6.3 Hz, 1H), 2.11 (tt, J = 17.6, 8.0 Hz, 4H),
			2.00-1.85 (m, 1H), 1.78 (t, J = 9.7 Hz, 1H), 1.69
			(t, J = 9.9 Hz, 1H).
70	2- phenylpropan- 2-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-
			phenylpropan-2-yl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 436 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 7.83 (s, 1H), 7.26
			(d, J = 4.2 Hz, 4H), 7.19-7.07 (m, 3H), 6.86 (d, J =
			8.0 Hz, 2H), 6.20-5.95 (m, 2H), 4.09 (d, J =
			5.8 Hz, 2H), 3.90 (h, J = 8.3 Hz, 1H), 3.72 (d, J =
			1.6 Hz, 3H), 2.98 (p, J = 8.4 Hz, 1H), 2.34 (dt, J =
			11.6, 6.4 Hz, 1H), 2.18-1.99 (m, 4H), 1.91 (t, J =
			9.7 Hz, 1H), 1.78 (t, J = 9.7 Hz, 1H), 1.66 (t, J =
			9.9 Hz, 1H), 1.51 (s, 6H).
71	1,2,3,4- tetrahydro- quinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(1,2,3,4-
			tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.34 (d, J = 9.1 Hz, 1H), 7.23-7.02
			(m, 5H), 6.86 (d, J = 8.0 Hz, 2H), 6.25-5.94 (m,
			2H), 4.09 (d, J = 5.7 Hz, 2H), 3.89 (q, J = 8.2 Hz,
			1H), 3.72 (s, 3H), 3.60 (t, J = 6.4 Hz, 2H), 3.39 (s,
			1H), 2.68 (t, J = 6.6 Hz, 2H), 2.31 (s, 1H), 2.15
			(qd, J = 12.1, 8.1, 6.5 Hz, 3H), 2.02-1.44 (m,
			6H).
72	7- (trifluoromethyl)- 1,2,3,4- tetrahydro- quinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(7-(trifluoromethyl)-
			1,2,3,4-tetrahydroisoquinoline-2-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 502 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.62 (d, J = 6.1 Hz, 1H), 7.51 (t, J =
			6.7 Hz, 1H), 7.39 (d, J = 8.0 Hz, 1H), 7.15 (d, J =
			8.0 Hz, 2H), 6.86 (d, J = 8.0 Hz, 2H), 6.23-6.02
			(m, 2H), 4.67 (s, 1H), 4.62 (s, 1H), 4.10 (d, J = 5.8
			Hz, 2H), 3.93 (q, J = 8.2 Hz, 1H), 3.67 (t, J = 6.0
			Hz, 1H), 3.72 (s, 3H), 3.58 (t, J = 5.9 Hz, 1H),
			3.33-3.25 (m, 1H), 2.89 (d, J = 5.9 Hz, 1H), 2.83
			(d, J = 6.1 Hz, 1H), 2.42 (dt, J = 11.9, 6.3 Hz, 1H),
			2.16 (dtt, J = 35.0, 12.7, 7.5 Hz, 5H), 1.83 (t, J =
			9.7 Hz, 1H), 1.70 (t, J = 9.7 Hz, 1H).
73	isoindoline	2.2
			1-(6-(isoindoline-2-carbonyl)spiro[3.3]heptan-2-
			yl)-3-(4-methoxybenzyl)urea. LRMS (APCI) m/z
			420 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.32 (dt, J = 14.8, 4.6 Hz, 4H), 7.16 (d, J = 8.0 Hz,
			2H), 6.87 (d, J = 8.0 Hz, 2H), 6.13 (t, J = 8.3 Hz,
			2H), 4.72 (s, 2H), 4.61 (s, 2H), 4.10 (d, J = 5.9 Hz,
			2H), 3.95 (h, J = 8.0 Hz, 1H), 3.72 (s, 3H), 3.24
			(p, J = 8.7 Hz, 1H), 2.42 (dt, J = 11.7, 6.2 Hz, 1H),
			2.35-1.99 (m, 5H), 1.85 (t, J = 9.7 Hz, 1H), 1.73
			(t, J = 10.0 Hz, 1H).
74	indoline	2.2
			1-(6-(indoline-1-carbonyl)spiro[3.3]heptan-2-
			yl)-3-(4-methoxybenzyl)urea. LRMS (APCI) m/z
			420 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			8.17 (d, J = 8.1 Hz, 1H), 7.32 (d, J = 7.5 Hz, 1H),
			7.31-7.18 (m, 3H), 7.08 (t, J = 7.5 Hz, 1H), 7.02-
			6.75 (m, 2H), 6.22 (d, J = 8.7 Hz, 2H), 4.21 (d, J =
			5.8 Hz, 2H), 4.06 (dt, J = 15.1, 8.2 Hz, 3H), 3.83
			(d, J = 1.8 Hz, 3H), 3.39 (q, J = 8.7 Hz, 1H), 3.22
			(t, J = 8.5 Hz, 2H), 2.52 (dt, J = 11.8, 6.3 Hz, 1H),
			2.30 (ddd, J = 47.0, 22.5, 9.6 Hz, 5H), 1.95 (t, J =
			9.7 Hz, 1H), 1.85 (t, J = 9.9 Hz, 1H).
75	2-(1H- pyrazol-4- yl)ethan-1- amine	2.2
			N-(2-(1H-pyrazol-4-yl)ethyl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 412 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 12.55 (s, 1H),
			7.71 (t, J = 5.7 Hz, 1H), 7.40 (s, 2H), 7.15 (d, J =
			8.0 Hz, 2H), 6.86 (d, J = 8.0 Hz, 2H), 6.29-5.86
			(m, 2H), 4.09 (d, J = 5.7 Hz, 2H), 3.91 (q, J = 8.0
			Hz, 1H), 3.72 (s, 3H), 3.28 (q, J = 6.8 Hz, 2H),
			3.17 (q, J = 6.8 Hz, 2H), 2.84 (p, J = 8.5 Hz, 1H),
			2.33 (dt, J = 11.7, 6.1 Hz, 1H), 2.24-2.02 (m,
			4H), 1.92 (dt, J = 11.1, 5.5 Hz, 1H), 1.78 (t, J = 9.7
			Hz, 1H), 1.69 (t, J = 10.0 Hz, 1H).
76	2- methyl-1- (piperazin-1- yl)propan- 2-ol	2.2
			1-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-
			1-carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 459
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.15
			(d, J = 7.9 Hz, 2H), 6.86 (d, J = 7.9 Hz, 2H), 6.19-
			5.98 (m, 2H), 4.15 (s, 1H), 4.09 (d, J = 5.9 Hz,
			2H), 3.90 (h, J = 8.2 Hz, 1H), 3.72 (s, 3H), 3.28 (d,
			J = 4.9 Hz, 2H), 3.32-3.28 (m, 2H), 3.16 (p, J =
			8.9 Hz, 1H), 2.40 (dp, J = 26.3, 6.2, 5.3 Hz, 5H),
			2.24-2.06 (m, 6H), 2.00 (t, J = 10.2 Hz, 1H), 1.79
			(t, J = 9.7 Hz, 1H), 1.68 (t, J = 9.9 Hz, 1H), 1.09
			(s, 6H).
77	4-(amino methyl)-3- fluorobenzo- nitrile	2.2
			N-(4-cyano-2-fluorobenzyl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 451 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.30 (t, J = 6.0 Hz,
			1H), 7.82 (d, J = 9.8 Hz, 1H), 7.68 (d, J = 7.9 Hz,
			1H), 7.42 (t, J = 7.7 Hz, 1H), 7.15 (d, J = 7.9 Hz,
			2H), 6.93-6.69 (m, 2H), 6.23-5.91 (m, 2H),
			4.33 (d, J = 5.7 Hz, 2H), 4.09 (d, J = 5.8 Hz, 2H),
			3.92 (h, J = 8.2 Hz, 1H), 3.72 (d, J = 1.6 Hz, 3H),
			2.95 (p, J = 8.4 Hz, 1H), 2.35 (dt, J = 11.6 Hz, 6.4 Hz,
			1H), 2.13 (dd, J = 19.9, 9.4 Hz, 4H), 1.98 (t, J =
			9.9 Hz, 1H), 1.79 (t, J = 9.7 Hz, 1H), 1.70 (t, J =
			10.0 Hz, 1H).
78	3- (pyridin-4- yl)cyclobutan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(3-(pyridin-4-
			yl)cyclobutyl)spiro[3.3]heptane-2-carboxamide.
			LRMS (APCI) m/z 449 (M + H). 1H NMR (400
			MHz, DMSO-d6); 1.1 ratio of diastereomers. δ
			8.48 (t, J = 4.4 Hz, 4H), 8.12 (d, J = 7.1 Hz, 1H),
			7.95 (d, J = 8.0 Hz, 1H), 7.30 (d, J = 4.9 Hz, 1H),
			7.26 (d, J = 5.0 Hz, 3H), 7.15 (d, J = 7.9 Hz, 4H),
			6.86 (d, J = 7.9 Hz, 4H), 6.21-5.98 (m, 4H), 4.24
			(dq, J = 16.8, 8.3, 7.9 Hz, 2H), 4.09 (d, J = 5.8 Hz,
			3H), 3.91 (h, J = 8.1 Hz, 2H), 3.72 (d, J = 1.5 Hz,
			6H), 3.14 (p, J = 9.3, 8.5 Hz, 2H), 2.82 (dp, J =
			25.2, 8.5 Hz, 2H), 2.59 (q, J = 8.7 Hz, 2H), 2.42-
			2.25 (m, 6H), 2.11 (tt, J = 14.5, 7.2 Hz, 8H), 1.96
			(dq, J = 19.9, 10.1 Hz, 4H), 1.79 (t, J = 9.7 Hz,
			2H), 1.69 (t, J = 10.0 Hz, 3H).
79	(R)-N- methyltetra- hydro furan-3-amine	2.2
			(R)-6-(3-(4-methoxybenzyl)ureido)-N-methyl-
			N-(tetrahydrofuran-3-yl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 402 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.23-7.04 (m,
			2H), 6.93-6.77 (m, 2H), 6.19-5.96 (m, 1H),
			5.14-4.97 (m, 1H), 4.45 (dq, J = 12.2, 5.9 Hz,
			1H), 4.09 (d, J = 5.8 Hz, 2H), 3.90 (p, J = 8.1 Hz,
			1H), 3.72 (d, J = 1.5 Hz, 3H), 3.59 (s, 3H), 3.27
			(q, J = 8.7 Hz, 2H), 3.16 (p, J = 8.6 Hz, 1H), 2.75
			(s, 2H), 2.68 (s, 2H), 2.38 (dq, J = 12.6, 6.9 Hz,
			1H), 2.13 (ddt, J = 37.2, 25.3, 11.7 Hz, 5H), 1.88-
			1.51 (m, 2H).
80	8-methyl- 2-(pyridin- 4-yl)propan- 1-amine	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(2-methyl-2-
			(pyridin-4-yl)propyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 451 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.46 (d, J = 4.9 Hz,
			2H), 7.46 (t, J = 6.4 Hz, 1H), 7.32 (d, J = 4.9 Hz,
			2H), 7.14 (d, J = 8.0 Hz, 2H), 6.86 (dd, J = 8.4, 1.7
			Hz, 2H), 6.21-5.96 (m, 2H), 4.09 (d, J = 5.8 Hz,
			2H), 3.88 (h, J = 7.9 Hz, 1H), 3.72 (d, J = 1.5 Hz,
			3H), 3.26 (d, J = 6.1 Hz, 2H), 2.85 (p, J = 8.4 Hz,
			1H), 2.30 (dt, J = 11.6, 6.5 Hz, 1H), 2.10 (dt, J =
			12.0, 6.3 Hz, 1H), 1.99 (dd, J = 20.8, 9.1 Hz, 3H),
			1.85 (t, J = 9.8 Hz, 1H), 1.75 (t, J = 9.7 Hz, 1H),
			1.65 (t, J = 10.0 Hz, 1H), 1.21 (s, 6H).
84	6- methyl-1,2,3,4- tetrahydro- quinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(6-methyl-1,2,3,4-
			tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 448 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.05-7.25 (m, 1H), 7.14 (d, J = 8.3
			Hz, 2H), 7.10-6.68 (m, 4H), 6.20-5.95 (m, 2H),
			4.08 (d, J = 5.8 Hz, 2H), 3.89 (q, J = 8.0 Hz, 1H),
			3.72 (s, 3H), 3.57 (t, J = 6.3 Hz, 2H), 3.38-3.20
			(m, 3H), 2.63 (s, 3H), 2.38-1.99 (m, 6H), 1.90-
			1.54 (m, 4H).
85	3,4- dihydro-2H- benzo[b] [1,4]oxazine	2.2
			1-(6-(3,4-dihydro-2H-benzo[b][1,4]oxazine-4-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 436
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.32-
			7.70 (m, 1H), 7.15 (d, J = 8.2 Hz, 2H), 7.02 (t, J =
			7.0 Hz, 1H), 6.87 (d, J = 8.2 Hz, 4H), 6.11 (q, J =
			8.3, 7.2 Hz, 2H), 4.22 (t, J = 4.5 Hz, 2H), 4.09 (d,
			J = 4.8 Hz, 2H), 3.92 (q, J = 6.8, 5.7 Hz, 1H), 3.72
			(s, 5H), 3.31 (s, 2H), 2.37 (s, 1H), 2.31-2.11 (m,
			3H), 2.07 (s, 1H), 1.81 (t, J = 9.7 Hz, 1H), 1.73
			(dd, J = 11.0, 8.8 Hz, 1H).
86	aniline	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-
			phenylspiro[3.3]heptane-2-carboxamide. LRMS
			(APCI) m/z 394 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 9.74 (s, 1H), 7.58 (d, J = 8.1 Hz, 2H),
			7.27 (t, J = 7.7 Hz, 2H), 7.15 (d, J = 8.3 Hz, 2H),
			7.01 (t, J = 7.4 Hz, 1H), 6.87 (d, J = 8.4 Hz, 2H),
			6.27-5.95 (m, 2H), 4.10 (d, J = 5.9 Hz, 2H), 3.94
			(h, J = 8.2 Hz, 1H), 3.73 (s, 3H), 3.09 (p, J = 8.4
			Hz, 1H), 2.46-2.32 (m, 1H), 2.30-2.09 (m, 4H),
			2.02 (ddd, J = 11.5, 8.2, 3.2 Hz, 1H), 1.83 (dd, J =
			10.6, 8.7 Hz, 1H), 1.74 (dd, J = 11.1, 8.8 Hz, 1H).
87	N- Methylaniline	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-methyl-N-
			phenylspiro[3.3]heptane-2-carboxamide. LRMS
			(APCI) m/z 408 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.44 (t, J = 7.5 Hz, 2H), 7.36 (t, J =
			7.4 Hz, 1H), 7.24 (d, J = 7.7 Hz, 2H), 7.13 (d, J =
			8.3 Hz, 2H), 6.85 (d, J = 8.2 Hz, 2H), 6.09 (t, J =
			6.0 Hz, 1H), 6.02 (d, J = 8.1 Hz, 1H), 4.07 (d, J =
			5.8 Hz, 2H), 3.82 (q, J = 8.1 Hz, 1H), 3.71 (s, 3H),
			3.13 (s, 3H), 2.84 (p, J = 8.7 Hz, 1H), 2.30-2.00
			(m, 4H), 1.78 (d, J = 10.2 Hz, 1H), 1.63 (q, J =
			10.5 Hz, 3H).
88	(2- difluoro methyl) pyridin-4- yl)methanamine	2.2
			N-((2-(difluoromethoxy)pyridin-4-yl)methyl)-6-
			(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-
			2-carboxamide. LRMS (APCI); m/z 475 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.30 (t, J = 6.0
			Hz, 1H), 8.18 (d, J = 5.2 Hz, 1H), 7.70 (t, J = 73.0
			Hz, 1H), 7.15 (d, J = 8.3 Hz, 2H), 7.10 (d, J = 5.2
			Hz, 1H), 6.87 (d, J = 8.6 Hz, 3H), 6.19-5.98 (m,
			2H), 4.29 (d, J = 5.9 Hz, 2H), 4.10 (d, J = 5.9 Hz,
			2H), 3.92 (h, J = 8.1 Hz, 1H), 3.72 (s, 3H), 2.97 (p,
			J = 8.4 Hz, 1H), 2.43-2.27 (m, 1H), 2.14 (dd, J =
			22.1, 8.8 Hz, 4H), 2.00 (t, J = 9.8 Hz, 1H), 1.80
			(dd, J = 10.7, 8.7 Hz, 1H), 1.71 (dd, J = 11.1, 8.8
			Hz, 1H).
89	[1,2,4] triazolo[4,3- a]pyridin- 6-amine	2.2
			N-([1,2,4]triazolo[4,3-a]pyridin-6-yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 435 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 10.06 (s, 1H),
			9.30 (d, J = 11.5 Hz, 2H), 7.76 (d, J = 9.7 Hz, 1H),
			7.28 (dd, J = 9.8, 1.7 Hz, 1H), 7.15 (d, J = 8.4 Hz,
			2H), 6.87 (d, J = 8.3 Hz, 2H), 6.22-6.01 (m, 2H),
			4.10 (d, J = 5.7 Hz, 2H), 3.95 (h, J = 8.3 Hz, 1H),
			3.72 (s, 3H), 3.14 (p, J = 8.0 Hz, 1H), 2.39 (ddd, J =
			11.4, 7.3, 5.2 Hz, 1H), 2.33-2.14 (m, 4H), 2.08
			(dd, J = 11.3, 8.4 Hz, 1H), 1.84 (dd, J = 10.7, 8.7
			Hz, 1H), 1.76 (dd, J = 11.1, 8.8 Hz, 1H).
90	1,2,3,4- tetrahydro- 1,6- naphthyridine	2.2
			1-(4-methoxybenzyl)-3-(6-(1,2,3,4-tetrahydro-
			1,6-naphthyridine-1-carbonyl)spiro[3.3]heptan-
			2-yl)urea. LRMS (APCI) m/z 435 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.22 (d, J = 4.5 Hz,
			1H), 8.16-7.74 (m, 1H), 7.19 (dd, J = 8.3, 4.8 Hz,
			1H), 7.15 (d, J = 8.2 Hz, 2H), 6.86 (d, J = 8.3 Hz,
			2H), 6.17-6.03 (m, 2H), 4.09 (d, J = 5.9 Hz, 2H),
			3.91 (q, J = 8.1 Hz, 1H), 3.72 (s, 3H), 3.68-3.58
			(m, 2H), 3.35-3.30 (m, 2H), 2.87 (t, J = 6.7 Hz,
			2H), 2.35 (d, J = 14.5 Hz, 1H), 2.29-2.10 (m,
			3H), 2.05 (s, 1H), 1.92 (p, J = 6.6 Hz, 2H), 1.80 (t,
			J = 9.8 Hz, 1H), 1.72 (t, J = 9.9 Hz, 1H).
91	(R)-2,3- dihydro-1H- inden-1- amine	2.2
			(R)-N-(2,3-dihydro-1H-inden-1-yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 434 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.01 (d, J = 8.2 Hz,
			1H), 7.27-7.08 (m, 5H), 6.87 (dd, J = 8.5, 3.0 Hz,
			2H), 6.15-6.05 (m, 2H), 5.26 (q, J = 8.6 Hz, 1H),
			4.10 (t, J = 4.0 Hz, 2H), 3.93 (q, J = 8.2 Hz, 1H),
			3.73 (d, J = 3.1 Hz, 3H), 2.96-2.71 (m, 3H), 2.40-
			2.29 (m, 1H), 2.34 (s, 2H), 2.16 (tt, J = 13.5,
			10.1, 8.8 Hz, 4H), 2.03-1.89 (m, 1H), 1.76 (dt, J =
			29.6, 10.0 Hz, 3H).
92	(S)-2,3- dihydro- 1H-inden-1- amine	2.2
			(S)-N-(2,3-dihydro-1H-inden-1-yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 434 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.00 (d, J = 8.2 Hz,
			1H), 7.27-7.12 (m, 6H), 6.87 (dd, J = 8.7, 2.4 Hz,
			2H), 6.16-6.04 (m, 2H), 5.25 (d, J = 8.4 Hz, 1H),
			4.10 (s, 2H), 3.96-3.87 (m, 1H), 3.73 (d, J = 3.0
			Hz, 3H), 2.96-2.86 (m, 2H), 2.78 (dt, J = 16.3,
			7.7 Hz, 1H), 2.35 (d, J = 10.0 Hz, 2H), 2.19 (p, J =
			10.0 Hz, 4H), 1.98 (s, 1H), 1.76 (dt, J = 29.8, 10.1
			Hz, 3H).
93	(3- amino- 2,3- dihydro-1H- inden-1- yl)methanol	2.2
			N-(3-(hydroxymethyl)-2,3-dihydro-1H-inden-1-
			yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 464 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.98 (d, J = 8.2
			Hz, 1H), 7.34 (d, J = 5.6 Hz, 1H), 7.26-7.01 (m,
			5H), 6.93-6.81 (m, 2H), 6.12 (dd, J = 13.5, 6.3
			Hz, 2H), 5.22 (q, J = 9.1 Hz, 1H), 4.79 (d, J = 4.4
			Hz, 1H), 4.10 (t, J = 4.1 Hz, 2H), 3.93 (q, J = 8.8
			Hz, 1H), 3.81-3.68 (m, 4H), 3.57 (q, J = 5.4 Hz,
			1H), 3.14 (t, J = 7.4 Hz, 1H), 3.02-2.84 (m, 1H),
			2.47 (d, J = 11.6 Hz, 1H), 2.35 (q, J = 8.1, 6.8 Hz,
			1H), 2.17 (dt, J = 22.2, 9.9 Hz, 4H), 2.06-1.89
			(m, 1H), 1.76 (dt, J = 29.4, 9.9 Hz, 2H), 1.53 (q, J =
			10.4 Hz, 1H).
94	3-amino- 2,3-dihydro- 1H-inden- 1-ol	2.2
			N-(1-hydroxy-2,3-dihydro-1H-inden-2-yl)-6-(3-
			(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 450 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.03 (d, J = 7.2
			Hz, 1H), 7.28 (t, J = 4.2 Hz, 1H), 7.18 (ddt, J =
			19.6, 8.6, 3.1 Hz, 5H), 6.92-6.72 (m, 2H), 6.18-
			5.99 (m, 2H), 5.51 (s, 1H), 4.92-4.80 (m, 1H),
			4.10 (d, J = 6.1 Hz, 3H), 3.93 (q, J = 8.0 Hz, 1H),
			3.72 (s, 3H), 3.13 (dd, J = 15.8, 8.0 Hz, 1H), 2.90
			(qd, J = 9.6, 4.8 Hz, 1H), 2.64-2.53 (m, 1H), 2.41-
			2.31 (m, 1H), 2.25-2.09 (m, 4H), 1.95 (ddd, J =
			11.6, 7.8, 3.5 Hz, 1H), 1.80 (t, J = 9.8 Hz, 1H),
			1.70 (dt, J = 29.4, 9.9 Hz, 1H).
95	2,3- dihydro-1H- inden-2- amine	2.2
			N-(2,3-dihydro-1H-inden-2-yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 434 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.04-7.84 (m,
			1H), 7.20 (t, J = 4.0 Hz, 2H), 7.15 (q, J = 3.3 Hz,
			4H), 6.87 (dd, J = 8.6, 2.7 Hz, 2H), 6.09 (dt, J =
			10.3, 6.5 Hz, 2H), 4.42 (q, J = 7.4 Hz, 1H), 4.09 (t,
			J = 4.3 Hz, 2H), 3.91 (q, J = 8.0 Hz, 1H), 3.73 (d, J =
			2.9 Hz, 3H), 3.14 (dd, J = 16.3, 7.5 Hz, 2H),
			2.94-2.79 (m, 1H), 2.78-2.61 (m, 2H), 2.33 (q,
			J = 6.4, 5.7 Hz, 1H), 2.23-2.00 (m, 4H), 1.92 (d,
			J = 9.9 Hz, 1H), 1.79 (d, J = 9.7 Hz, 1H), 1.70 (t, J =
			10.2 Hz, 1H).
96	(R)- 1,2,3,4- tetrahydro- naphthalen-2- amine	2.2
			(R)-6-(3-(4-methoxybenzyl)ureido)-N-(1,2,3,4-
			tetrahydronaphthalen-2-yl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 448 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.71 (dd, J =
			7.8, 3.1 Hz, 1H), 7.24-7.12 (m, 2H), 7.08 (d, J =
			3.7 Hz, 4H), 6.87 (dd, J = 8.5, 3.0 Hz, 2H), 6.23-
			5.95 (m, 2H), 4.10 (t, J = 4.2 Hz, 2H), 3.91 (t, J =
			8.6 Hz, 2H), 3.73 (d, J = 3.3 Hz, 3H), 3.04-2.84
			(m, 2H), 2.85-2.69 (m, 2H), 2.57 (dd, J = 16.8,
			10.5 Hz, 1H), 2.34 (h, J = 4.2 Hz, 1H), 2.13 (p, J =
			10.1, 9.6 Hz, 4H), 2.01-1.85 (m, 2H), 1.84-1.75
			(m, 1H), 1.75-1.66 (m, 1H), 1.66-1.50 (m, 1H).
97	(S)-7- fluoro- 1,2,3,4- tetrahydro- naphthalen- 1-amine	2.2
			(S)-N-(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-
			yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 466 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.06 (d, J = 8.5
			Hz, 1H), 7.15 (p, J = 3.3 Hz, 3H), 7.00 (d, J = 8.9
			Hz, 1H), 6.92-6.71 (m, 3H), 6.21-5.97 (m, 2H),
			4.93 (s, 1H), 4.10 (t, J = 4.5 Hz, 2H), 3.93 (q, J =
			8.3 Hz, 1H), 3.72 (d, J = 2.1 Hz, 3H), 3.06-2.83
			(m, 1H), 2.69 (s, 2H), 2.34 (s, 1H), 2.18 (p, J =
			10.3, 9.9 Hz, 4H), 1.95 (t, J = 9.8 Hz, 1H), 1.90-
			1.78 (m, 4H), 1.71 (d, J = 9.7 Hz, 1H), 1.60 (q, J =
			9.8 Hz, 1H).
98	(S)-6- fluoro- 1,2,3,4- tetrahydro- naphthalen-1- amine	2.2
			(S)-N-(6-fluoro-1,2,3,4-tetrahydronaphthalen-1-
			yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 466 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.00 (dd, J =
			8.5, 4.2 Hz, 1H), 7.27-7.04 (m, 3H), 6.94 (dd, J =
			18.8, 7.6 Hz, 2H), 6.87 (dd, J = 8.2, 2.7 Hz, 2H),
			6.10 (q, J = 8.9, 7.7 Hz, 2H), 4.92 (s, 1H), 4.10 (t,
			J = 4.2 Hz, 2H), 3.92 (q, J = 8.5 Hz, 1H), 3.73 (t, J =
			2.2 Hz, 3H), 2.91 (t, J = 8.3 Hz, 1H), 2.82-2.63
			(m, 2H), 2.32 (t, J = 7.7 Hz, 1H), 2.16 (dq, J =
			19.8, 9.9, 9.5 Hz, 4H), 1.97 (t, J = 10.9 Hz, 1H),
			1.89-1.53 (m, 6H).
99	(R)-7- fluoro- 1,2,3,4- tetrahydro- naphthalen-1- amine	2.2
			(R)-N-(7-fluoro-1,2,3,4-tetrahydronaphthalen- 1-yl)-6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 466 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 8.06 (d, J = 8.5
			Hz, 1H), 7.27-7.06 (m, 3H), 6.99 (s, 1H), 6.85 (t,
			J = 11.7 Hz, 3H), 6.08 (d, J = 11.3 Hz, 2H), 4.92
			(d, J = 7.9 Hz, 1H), 4.10 (t, J = 4.2 Hz, 2H), 3.93
			(d, J = 9.6 Hz, 1H), 3.73 (d, J = 3.3 Hz, 3H), 2.92
			(dd, J = 13.3, 5.8 Hz, 1H), 2.69 (s, 2H), 2.34 (s,
			1H), 2.17 (d, J = 10.9 Hz, 4H), 1.97 (d, J = 9.4 Hz,
			1H), 1.91-1.51 (m, 6H).
100	(R)- 1,2,3,4- tetrahydro- naphthalen- 1-amine	2.2
			(R)-6-(3-(4-methoxybenzyl)ureido)-N-(1,2,3,4-
			tetrahydronaphthalen-1-yl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 448 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.00 (dt, J = 8.2,
			3.6 Hz, 1H), 7.22-7.01 (m, 6H), 6.87 (dd, J = 7.9,
			3.2 Hz, 2H), 6.26-5.86 (m, 2H), 4.94 (d, J = 8.2
			Hz, 1H), 4.10 (t, J = 4.3 Hz, 2H), 3.92 (q, J = 8.5
			Hz, 1H), 3.73 (d, J = 3.4 Hz, 3H), 2.91 (tt, J = 9.9,
			5.0 Hz, 1H), 2.71 (s, 2H), 2.33 (q, J = 7.7, 6.9 Hz,
			1H), 2.16 (tt, J = 12.5, 7.0 Hz, 4H), 1.97 (dd, J =
			15.1, 9.4 Hz, 1H), 1.91-1.39 (m, 6H).
101	6- fluoro- 1,2,3,4- tetrahydro- quinoline	2.2
			1-(6-(6-fluoro-1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. MS (APCI) m/z 452
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.47 (s,
			1H), 7.15 (dt, J = 8.5, 5.1 Hz, 3H), 7.02-6.74 (m,
			3H), 6.24-5.86 (m, 2H), 4.09 (t, J = 4.2 Hz, 2H),
			3.92 (q, J = 8.5 Hz, 1H), 3.72 (d, J = 3.2 Hz, 3H),
			3.59 (dt, J = 7.5, 4.5 Hz, 2H), 3.43 (tt, J = 10.7, 5.5
			Hz, 1H), 2.70 (d, J = 7.1 Hz, 2H), 2.36 (s, 1H),
			2.18 (dt, J = 14.5, 6.7 Hz, 3H), 2.02 (s, 1H), 1.82
			(dq, J = 16.9, 9.4, 7.1 Hz, 4H), 1.76-1.66 (m,
			1H).
102	7,8- difluoro- 1,2,3,4- tetrahydro- quinoline	2.2
			1-(6-(7,8-difluoro-1,2,3,4-tetrahydroquinoline-
			1-carbonyl)spiro[3.3[heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 470
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.15
			(d, J = 7.9 Hz, 3H), 6.87 (d, J = 7.8 Hz, 3H), 6.10
			(d, J = 9.5 Hz, 2H), 4.09 (s, 2H), 3.73 (d, J = 2.9
			Hz, 4H), 3.17 (d, J = 3.1 Hz, 2H), 2.68 (s, 2H),
			2.34 (s, 2H), 2.17 (s, 2H), 1.76 (d, J = 35.3 Hz,
			3H), 1.25 (s, 4H).
103	6- (difluoro methoxy)- 1,2,3,4- tetrahydro- quinoline	2.2
			1-(6-(6-(difluoromethoxy)-1,2,3,4-
			tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 500
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.34
			(br s, 1H), 7.30-7.18 (m, 3H), 6.99 (d, J = 13.8 Hz,
			2H), 6.86 (dd, J = 8.5, 2.9 Hz, 2H), 6.08 (d, J =
			11.9 Hz, 2H), 4.09 (d, J = 4.6 Hz, 2H), 4.03-3.76
			(m, 1H), 3.72 (d, J = 3.0 Hz, 3H), 3.60 (d, J = 7.0
			Hz, 2H), 2.70 (d, J = 8.4 Hz, 2H), 2.34 (s, 1H),
			2.27-1.91 (m, 6H), 1.90-1.56 (m, 4H).
104	6- (trifluoromethyl)- 1,2,3,4- tetrahydroquinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(6-(trifluoromethyl)-
			1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 502 (M + H).
105	5- fluoro- 1,2,3,4- tetrahydroquinoline	2.2
			1-(6-(5-fluoro-1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 452
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.34 (s,
			1H), 7.25-7.05 (m, 3H), 6.95 (d, J = 9.2 Hz, 1H),
			6.90-6.76 (m, 2H), 6.23-5.95 (m, 2H), 4.09 (d,
			J = 4.6 Hz, 2H), 4.00-3.83 (m, 1H), 3.72 (d, J =
			3.1 Hz, 3H), 3.61 (d, J = 5.2 Hz, 2H), 3.42 (q, J =
			9.0 Hz, 1H), 2.70 (d, J = 8.2 Hz, 2H), 2.34 (s, 1H),
			2.19 (dd, J = 19.3, 9.3 Hz, 4H), 2.01 (s, 1H), 1.91-
			1.57 (m, 4H).
106	7- fluoro- 1,2,3,4- tetrahydroquinoline	2.2
			1-(6-(7-fluoro-1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 452
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.47 (s,
			1H), 7.15 (dt, J = 8.5, 5.1 Hz, 3H), 6.98-6.73 (m,
			3H), 6.22-5.96 (m, 2H), 4.09 (t, J = 4.2 Hz, 2H),
			3.92 (q, J = 8.5 Hz, 1H), 3.72 (d, J = 3.1 Hz, 3H),
			3.65-3.52 (m, 2H), 3.45 (tt, J = 9.0, 5.1 Hz, 1H),
			2.70 (d, J = 7.1 Hz, 2H), 2.36 (s, 1H), 2.18 (dt, J =
			14.5, 6.7 Hz, 4H), 2.02 (s, 1H), 1.82 (dq, J = 16.9,
			9.4, 7.1 Hz, 3H), 1.76-1.61 (m, 1H).
107	6- (trifluoromethoxy)- 1,2,3,4- tetrahydroquinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(6-
			(trifluoromethoxy)-1,2,3,4-tetrahydroquinoline-
			1-carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 518 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.45 (s, 1H), 7.11 (t, J = 8.5 Hz, 3H),
			7.00-6.4 (m, 3H), 6.24-5.99 (m, 2H), 4.13 (t, J =
			4.2 Hz, 2H), 3.78 (q, J = 8.5 Hz, 1H), 3.72 (d, J =
			3.2 Hz, 3H), 3.45 (dt, J = 7.5, 4.5 Hz, 2H), 3.32
			(tt, J = 10.7, 5.5 Hz, 1H), 2.78 (d, J = 7.1 Hz, 2H),
			2.36 (s, 1H), 2.18 (dt, J = 14.5, 6.7 Hz, 3H), 2.02
			(s, 1H), 1.82 (dq, J = 16.9, 9.4, 7.1 Hz, 4H), 1.76-
			1.66 (m, 1H).
108	7- methyl- 1,2,3,4- tetrahydroquinoline	2.2
			1-(4-methoxybenzyl)-3-(6-(7-methyl-1,2,3,4-
			tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 448 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.45 (s, 1H), 7.20-7.11 (m, 2H),
			7.09-7.00 (m, 1H), 6.96-6.80 (m, 3H), 6.18-
			6.03 (m, 2H), 4.09 (t, J = 4.1 Hz, 2H), 3.90 (q, J =
			8.9, 8.4 Hz, 1H), 3.72 (d, J = 3.1 Hz, 3H), 3.58 (d,
			J = 7.1 Hz, 2H), 2.64 (d, J = 7.5 Hz, 2H), 2.30 (s,
			2H), 2.27 (d, J = 3.0 Hz, 3H), 2.23-2.07 (m, 3H),
			1.96 (s, 1H), 1.88-1.61 (m, 5H).
109	2- methyl-1- (piperazin- 1-yl)propan-2- ol	2.3
			1-(4-fluorobenzyl)-3-(6-(4-(2-hydroxy-2-
			methylpropyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 447 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.26 (dd, J = 8.6, 5.7 Hz, 2H), 7.13
			(t, J = 8.9 Hz, 2H), 6.23 (t, J = 6.0 Hz, 1H), 6.15
			(d, J = 8.0 Hz, 1H), 5.29 (s, 1H), 4.15 (d, J = 6.0
			Hz, 2H), 3.91 (q, J = 8.0 Hz, 1H), 3.84-3.64 (m,
			1H), 3.48 (s, 1H), 3.12 (s, 1H), 2.47-2.32 (m,
			3H), 2.29-2.08 (m, 7H), 2.02 (s, 1H), 1.81 (t, J =
			9.7 Hz, 1H), 1.71 (t, J = 10.0 Hz, 1H), 1.25 (s,
			3H), 1.09 (s, 6H).
110	2-methyl- 1- (piperazin-1- yl)propan-2- ol	2.1
			1-(4-chlorophenyl)-3-(6-(4-(2-hydroxy-2-
			methylpropyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 464 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.44-7.27 (m, 2H), 7.24 (d, J = 8.4
			Hz, 2H), 6.26 (t, J = 6.0 Hz, 1H), 6.18 (d, J = 8.0
			Hz, 1H), 4.15 (d, J = 6.1 Hz, 3H), 3.91 (q, J = 8.1
			Hz, 1H), 3.20 (br s, 4H), 2.48-2.28 (m, 6H), 2.14
			(dd, J = 19.9, 9.0 Hz, 6H), 2.01 (t, J = 10.0 Hz,
			1H), 1.89-1.76 (m, 1H), 1.71 (t, J = 9.8 Hz, 1H),
			1.17 (d, J = 60.5 Hz, 6H).
111	1- (oxetan-3- yl)piperazine	2.2
			1-(4-methoxybenzyl)-3-(6-(4-(oxetan-3-
			yl)piperazine-1-carbonyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 443 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 7.15 (d, J = 8.5 Hz, 2H),
			6.86 (d, J = 8.6 Hz, 2H), 6.20-5.99 (m, 2H), 4.53
			(t, J = 6.5 Hz, 2H), 4.43 (t, J = 6.1 Hz, 2H), 4.09
			(d, J = 6.0 Hz, 2H), 3.91 (h, J = 8.2 Hz, 1H), 3.72
			(s, 3H), 3.44 (q, J = 3.9 Hz, 2H), 3.31 (d, J = 5.6
			Hz, 3H), 3.19 (p, J = 8.6 Hz, 1H), 2.37 (ddd, J =
			10.8, 7.5, 5.3 Hz, 1H), 2.15 (dtd, J = 21.8, 8.2, 7.5,
			3.6 Hz, 8H), 2.01 (ddd, J = 11.4, 8.6, 2.8 Hz, 1H),
			1.79 (dd, J = 10.8, 8.6 Hz, 1H), 1.69 (dd, J = 11.1,
			8.7 Hz, 1H).
112	1- (cyclopropyl- methyl) piperazine	2.2
			1-(6-(4-(cyclopropylmethyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 441
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.15
			(d, J = 8.6 Hz, 2H), 6.87 (d, J = 8.6 Hz, 2H), 6.26-
			6.00 (m, 2H), 4.09 (d, J = 5.8 Hz, 2H), 4.00-
			3.74 (m, 1H), 3.72 (s, 4H), 3.24-3.31 (m, 5H), 3.04
			(d, J = 16.1 Hz, 1H), 2.90-2.60 (m, 3H), 2.38
			(ddd, J = 10.7, 7.4, 5.3 Hz, 1H), 2.28-2.08 (m,
			5H), 2.04 (ddd, J = 11.4, 8.5, 3.0 Hz, 1H), 1.81
			(dd, J = 10.7, 8.7 Hz, 1H), 1.71 (dd, J = 11.1, 8.8
			Hz, 1H), 0.99 (tq, J = 7.3, 3.7, 2.6 Hz, 1H), 0.73-
			0.52 (m, 2H), 0.30 (t, J = 4.9 Hz, 2H).
113	(4- methylpiperazin- 2-yl)methanol	2.2
			1-(6-(2-(hydroxymethyl)-4-methylpiperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 431
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.63
			(d, J = 8.3 Hz, 2H), 7.15 (d, J = 8.6 Hz, 2H), 6.86
			(d, J = 8.6 Hz, 1H), 6.23-6.01 (m, 1H), 4.30 (s,
			1H), 4.16 (d, J = 13.5 Hz, 2H), 4.09 (d, J = 5.9 Hz,
			2H), 4.01-3.85 (m, 1H), 3.72 (s, 3H), 3.67-3.54
			(m, 2H), 3.27 (t, J = 8.8 Hz, 1H), 3.04 (ddd, J =
			16.2, 7.8, 3.2 Hz, 2H), 2.92 (d, J = 11.4 Hz, 2H),
			2.81 (d, J = 11.5 Hz, 1H), 2.75-2.63 (m, 2H),
			2.37 (ddt, J = 10.4, 7.6, 4.5 Hz, 1H), 2.17 (s, 1H),
			2.16-2.09 (m, 3H), 1.83 (dddd, J = 24.4, 15.5,
			12.3, 6.3 Hz, 2H), 1.69 (ddq, J = 12.0, 9.3, 3.6, 3.1
			Hz, 2H).
122	1-isopropyl- piperazine	2.2
			1-(6-(4-isopropylpiperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 429
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.14 (d,
			J = 8.6 Hz, 2H), 6.86 (d, J = 8.6 Hz, 2H), 6.23-
			5.92 (m, 2H), 4.09 (d, J = 6.0 Hz, 2H), 3.99-3.84
			(m, 1H), 3.72 (s, 3H), 3.34 (t, J = 4.8 Hz, 2H),
			3.27 (t, J = 4.8 Hz, 2H), 3.17 (p, J = 8.5 Hz, 1H),
			2.67 (dd, J = 9.5, 4.1 Hz, 1H), 2.37 (tt, J = 8.9, 4.0
			Hz, 5H), 2.25-2.08 (m, 4H), 2.01 (ddd, J = 11.4,
			8.6, 2.8 Hz, 1H), 1.79 (dd, J = 10.8, 8.7 Hz, 1H),
			1.68 (dd, J = 11.1, 8.7 Hz, 1H), 0.96 (d, J = 6.5 Hz,
			6H).
123	1-((1- methyl-1H- pyrazol-4- yl)methyl) yl)piperazine	2.2
			1-(4-methoxybenzyl)-3-(6-(4-((1-methyl-1H-
			pyrazol-4-yl)methyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 481 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.58 (s, 1H), 7.31 (s, 1H), 7.14 (d, J =
			8.7 Hz, 2H), 6.86 (d, J = 8.5 Hz, 2H), 6.21-5.94
			(m, 2H), 4.09 (d, J = 5.9 Hz, 2H), 3.90 (td, J = 8.8,
			7.7, 5.9 Hz, 1H), 3.79 (s, 3H), 3.56 (s, 4H), 3.30
			(brs, 8H), 3.17 (p, J = 8.6 Hz, 1H), 2.36 (ddd, J =
			12.7, 7.1, 3.5 Hz, 1H), 2.21-2.06 (m, 5H), 2.00
			(ddd, J = 11.5, 8.6, 3.0 Hz, 1H), 1.78 (dd, J = 10.7,
			8.7 Hz, 1H), 1.68 (dd, J = 11.1, 8.7 Hz, 1H).
124	1-(pyridin- 4-ylmethyl) piperazine	2.2
			1-(4-methoxybenzyl)-3-(6-(4-(pyridin-4-
			ylmethyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 478 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.58 (d, J = 7.6 Hz, 2H), 7.72 (dd, J =
			7.6, 1.8 Hz, 2H), 7.13 (d, J = 8.9 Hz, 2H), 6.90 (d,
			J = 8.9 Hz, 2H), 6.29-5.99 (m, 2H), 4.11 (d, J =
			5.9 Hz, 2H), 3.91-3.82 (m, 1H), 3.73 (s, 3H),
			3.64 (s, 3H), 3.41 (d, J = 5.3 Hz, 3H), 3.16 (p, J =
			8.6 Hz, 1H), 2.40-2.21 (m, 4H), 2.22-2.1 (m,
			5H), 2.09 (ddd, J = 11.5, 8.5, 2.8 Hz, 1H), 1.84
			(dd, J = 10.7, 8.6 Hz, 1H), 1.75 (dd, J = 11.0, 8.7
			Hz, 1H).
125	1-(pyridin- 2-ylmethyl) piperazine	2.2
			1-(4-methoxybenzyl)-3-(6-(4-(pyridin-2-
			ylmethyl)piperazine-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 478 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.51 (d, J = 4.6 Hz, 1H), 7.78 (td, J =
			7.6, 1.8 Hz, 1H), 7.45 (d, J = 7.7 Hz, 1H), 7.28
			(dd, J = 7.4, 5.0 Hz, 1H), 7.14 (d, J = 8.5 Hz, 2H),
			6.86 (d, J = 8.5, 2H), 6.28-5.94 (m, 2H), 4.09
			(d, J = 5.9 Hz, 2H), 4.00-3.82 (m, 1H), 3.72 (s,
			3H), 3.67 (s, 3H), 3.46 (d, J = 5.3 Hz, 3H), 3.18 (p,
			J = 8.6 Hz, 1H), 2.48-2.28 (m, 5H), 2.25-2.07
			(m, 4H), 2.01 (ddd, J = 11.5, 2.8 Hz, 1H), 1.79
			(dd, J = 10.7, 8.6 Hz, 1H), 1.69 (dd, J = 11.0, 8.7
			Hz, 1H).
126	(1-methyl- piperazin-2- yl)methanol	2.2
			6-(3-(4-methoxybenzyl)ureido)-N-(1-
			phenylcyclopropyl)spiro[3.3]heptane-2-
			carboxamide. LRMS (APCI) m/z 431 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.14 (d, J = 8.5
			Hz, 2H), 6.86 (d, J = 8.6 Hz, 2H), 6.21-5.95 (m,
			2H), 4.81 (s, 1H), 4.29 (d, J = 13.0 Hz, 1H), 4.09
			(d, J = 5.9 Hz, 2H), 4.03-3.85 (m, 1H), 3.72 (s,
			3H), 3.68-3.49 (m, 6H), 3.19 (td, J = 8.2, 2.9 Hz,
			1H), 3.11-3.01 (m, 1H), 2.96-2.84 (m, 1H),
			2.84-2.69 (m, 1H), 2.31 (d, J = 6.9 Hz, 2H), 2.26-
			1.90 (m, 6H), 1.80 (t, J = 9.6 Hz, 1H), 1.69 (dd, J =
			11.0, 8.7 Hz, 1H).
202	(S)-N- methyl- tetrahydro furan-3- amine	2.4
			(2S,4s,6S)-6-(3-(4-chlorobenzyl)ureido)-N-
			methyl-N-((R)-tetrahydrofuran-3-
			yl)spiro[3.3]heptane-2-carboxamide. LRMS
			(APCI) m/z 406 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.20 (d, J = 8.5 Hz, 2H), 7.15 (d, J =
			8.5 Hz, 2H), 5.05 (ddd, J = 11.0, 9.2, 4.9 Hz,
			1H), 4.53-4.38 (m, 1H), 4.17 (s, 2H), 4.00-3.86
			(m, 2H), 3.68-3.60 (m, 2H), 3.56 (tt, J = 8.3, 4.2
			Hz, 1H), 2.78 (s, 2H), 2.72 (s, 1H), 2.43 (dq, J =
			11.9, 6.2 Hz, 1H), 2.28-1.99 (m, 6H), 1.81 (ddt, J =
			13.3, 8.2, 4.3 Hz, 2H), 1.76-1.66 (m, 1H).
230	1- methylpiperazine	2.2
			1-(4-methoxybenzyl)-3-(6-(4-methylpiperazine-
			1-carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 401.1 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.19 (d, J = 8.3 Hz, 2H), 6.87 (d, J =
			8.3 Hz, 2H), 4.23 (s, 2H), 4.04 (p, J = 8.1 Hz, 1H),
			3.78 (s, 3H), 3.76-3.62 (m, 2H), 3.57 (t, J = 5.1
			Hz, 2H), 3.29 (d, J = 8.6 Hz, 1H), 3.29 (q, J = 5.5
			Hz, 4H), 2.58 (s, 3H), 2.53 (dt, J = 11.7, 6.4 Hz,
			1H), 2.40-2.22 (m, 4H), 2.14 (ddd, J = 11.7, 8.5,
			3.2 Hz, 1H), 1.96-1.87 (m, 1H), 1.87-1.75 (m,
			1H).
231	methyl piperazine-1- carboxylate	2.2
			methyl 4-(6-(3-(4-
			methoxybenzyl)ureido)spiro[3.3]heptane-2-
			carbonyl)piperazine-1-carboxylate. LRMS
			(APCI) m/z 445.1 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.61 (s, 1H), 7.09 (d, J = 8.3 Hz,
			2H), 6.76 (d, J = 8.3 Hz, 2H), 4.14 (s, 2H), 3.95
			(p, J = 8.2 Hz, 1H), 3.69 (s, 3H), 3.63 (s, 3H), 3.47
			(d, J = 4.9 Hz, 2H), 3.35 (dd, J = 20.6, 5.4 Hz,
			6H), 3.16 (p, J = 8.6 Hz, 1H), 2.44 (dt, J = 11.6,
			6.5 Hz, 1H), 2.29-2.15 (m, 4H), 2.04 (dd, J =
			12.0, 8.9 Hz, 1H), 1.85-1.76 (m, 1H), 1.71 (dd, J =
			11.1, 9.0 Hz, 1H).
232	thiomorpholine 1,1-dioxide	2.2
			1-(6-(1,1-dioxoidothiomorpholine-4-
			carbonyl)spiro[3.3]heptan-2-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z 436.2
			(M + H). 1H NMR (400 MHz, Methanol-d4) δ 7.10
			(d, J = 8.3 Hz, 2H), 6.76 (d, J = 8.4 Hz, 2H), 4.14
			(s, 2H), 3.95 (q, J = 8.8, 8.0 Hz, 3H), 3.78 (t, J =
			5.2 Hz, 2H), 3.69 (s, 3H), 3.18 (q, J = 8.6 Hz, 1H),
			3.05-2.93 (m, 4H), 2.45 (dt, J = 11.5, 6.5 Hz,
			1H), 2.23 (ddd, J = 18.0, 10.3, 5.1 Hz, 4H), 2.11-
			2.00 (m, 1H), 1.81 (dd, J = 11.0, 8.6 Hz, 1H), 1.72
			(dd, J = 11.1, 9.0 Hz, 1H).
233	methyl piperazine- 1-carboxylate	2.1
			Methyl 4-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptane-2-
			carbonyl)piperazine-1-carboxylate. LRMS
			(APCI) m/z 449.1 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.32 (d, J = 7.6 Hz, 2H), 7.26 (d, J =
			8.2 Hz, 2H), 4.28 (s, 2H), 4.03 (p, J = 7.9 Hz,
			1H), 3.72 (s, 3H), 3.57 (t, J = 5.2 Hz, 2H), 3.46 (d,
			J = 8.9 Hz, 6H), 3.30 (d, J = 9.0 Hz, 1H), 2.54 (dt,
			J = 11.4, 6.2 Hz, 1H), 2.30 (dt, J = 20.8, 9.9 Hz,
			4H), 2.20-2.08 (m, 1H), 1.98-1.88 (m, 1H),
			1.88-1.73 (m, 1H).
234	2-methyl- 1-(piperazin- 1-yl)propan-2-ol	13.1
			1-(4-chlorobenzyl)-3-(6-(2-(4-(2-hydoxy-2-
			methylpropyl)piperazin-1-yl)-2-
			oxoethyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 477.0 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.31 (d, J = 7.9 Hz, 2H), 7.26 (d,
			J = 8.1 Hz, 2H), 4.28 (s, 2H), 4.02 (p, J = 7.8 Hz,
			1H), 3.67 (p, J = 4.7 Hz, 4H), 2.90 (d, J = 23.7 Hz,
			4H), 2.66 (s, 2H), 2.60-2.42 (m, 4H), 2.28 (dt, J =
			11.3, 5.9 Hz, 2H), 2.11 (dd, J = 10.6, 6.2 Hz,
			1H), 1.94-1.67 (m, 4H), 1.27 (s, 6H).
235	(S)- pyrrolidin- 2-ylmethanol	13.1
			(S)-1-(4-chlorobenzyl)-3-(6-(2-(2-(hydroxymethyl)
			pyrrolidin-1-yl)-2-oxoethyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 420.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 7.31 (d, J = 7.9
			Hz, 2H), 7.26 (d, J = 8.1 Hz, 2H), 4.28 (s, 2H),
			4.08 (p, J = 4.7 Hz, 1H), 4.01 (q, J = 7.7 Hz, 1H),
			3.63 (dd, J = 10.8, 4.0 Hz, 1H), 3.53 (dt, J = 18.1,
			6.3 Hz, 3H), 2.57 (p, J = 7.6 Hz, 1H), 2.52-2.36
			(m, 3H), 2.29 (dq, J = 12.1, 5.6, 5.0 Hz, 2H), 2.12
			(ddd, J = 11.9, 7.6, 4.0 Hz, 1H), 2.07-1.86 (m,
			5H), 1.86-1.70 (m, 3H).
236	pyrrolidine	13.1
			1-(4-chlorobenzyl)-3-(6-(2-oxo-2-(pyrrolidin-1-
			yl)ethyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 390.2 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.31 (d, J = 7.9 Hz, 2H), 7.26 (d, J =
			8.1 Hz, 2H), 4.28 (s, 2H), 4.08 (p, J = 4.7 Hz,
			1H), 4.01 (q, J = 7.7 Hz, 1H), 3.63 (dd, J = 10.8,
			4.0 Hz, 1H), 3.53 (dt, J = 18.1, 6.3 Hz, 3H), 2.57
			(p, J = 7.6 Hz, 1H), 2.52-2.36 (m, 3H), 2.29 (dq,
			J = 12.1, 5.6, 5.0 Hz, 2H), 2.12 (ddd, J = 11.9, 7.6,
			4.0 Hz, 1H), 2.07-1.86 (m, 5H), 1.86-1.70 (m,
			3H).
237	N-methyl- 1- phenyl- methanamine	13.2
			N-benzyl-2-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-N-
			methylpropanamide. LRMS (APCI) m/z 454.1
			(M + H). 1H NMR (400 MHz, Methanol-d4) δ 7.23-
			7.16 (m, 4H), 7.16-7.06 (m, 5H), 4.66-4.50
			(m, 2H), 4.16 (s, 2H), 3.89 (dt, J = 18.2, 8.7 Hz,
			1H), 2.88 (dd, J = 31.5, 3.8 Hz, 3H), 2.78-2.55
			(m, 1H), 2.42-2.26 (m, 2H), 2.15-1.85 (m, 3H),
			1.79-1.52 (m, 4H), 0.96-0.87 (m, 3H).
256	1,2,3,4- tetrahydro- quinoline	2.6
			1-(4-chlorobenzyl)-3-(5-(3,4-dihydroquinolin-
			1(2H)-yl)-5-oxopentyl)urea. LRMS (APCI) m/z
			400.1 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.42 (s, 1H), 7.36 (d, J = 8.4 Hz, 2H), 7.25 (d, J =
			8.3 Hz, 2H), 7.23-7.12 (m, 2H), 7.08 (t, J = 7.4
			Hz, 1H), 6.31 (t, J = 6.1 Hz, 1H), 5.94 (t, J = 5.7
			Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H), 3.67 (t, J = 6.4
			Hz, 2H), 2.97 (q, J = 6.5 Hz, 2H), 2.69 (t, J = 6.7
			Hz, 2H), 2.47 (d, J = 7.3 Hz, 2H), 1.87 (q, J = 6.5
			Hz, 2H), 1.58-1.46 (m, 2H), 1.34 (t, J = 7.6 Hz,
			2H).
257	cyclo- hexanamine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-
			cyclohexylhexanamide. LRMS (APCI) m/z 380.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.59
			(d, J = 8.0 Hz, 1H), 7.37 (d, J = 8.4 Hz, 2H), 7.25
			(d, J = 8.4 Hz, 2H), 6.30 (t, J = 6.1 Hz, 1H), 5.92
			(t, J = 5.6 Hz, 1H), 4.17 (d, J = 6.0 Hz, 2H), 3.56-
			3.43 (m, 1H), 2.98 (q, J = 6.6 Hz, 2H), 2.02 (t, J =
			7.4 Hz, 2H), 1.78-1.61 (m, 4H), 1.59-1.42 (m,
			3H), 1.36 (p, J = 7.2 Hz, 2H), 1.28-1.17 (m, 4H),
			1.12 (t, J = 11.8 Hz, 3H).
258	cyclo- pentanamine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-
			cyclopentylhexanamide. LRMS (APCI) m/z
			366.2 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.68 (d, J = 7.2 Hz, 1H), 7.37 (d, J = 8.4 Hz, 2H),
			7.25 (d, J = 8.4 Hz, 2H), 6.31 (t, J = 6.1 Hz, 1H),
			5.92 (t, J = 5.6 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H),
			3.97 (q, J = 6.9 Hz, 1H), 2.98 (q, J = 6.6 Hz, 2H),
			2.01 (t, J = 7.4 Hz, 2H), 1.77 (dq, J = 12.4, 6.5 Hz,
			2H), 1.60 (dq, J = 11.0, 6.6, 5.7 Hz, 2H), 1.56-
			1.40 (m, 4H), 1.40-1.28 (m, 4H), 1.22 (dt, J =
			11.8, 6.9 Hz, 2H).
259	morpholine	2.7
			1-(4-chlorobenzyl)-3-(6-morpholine-6-
			oxohexyl)urea. LRMS (APCI) m/z 368.1 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.37 (d, J = 8.4
			Hz, 2H), 7.26 (d, J = 8.4 Hz, 2H), 6.31 (t, J = 6.1
			Hz, 1H), 5.93 (t, J = 5.6 Hz, 1H), 4.18 (d, J = 5.9
			Hz, 2H), 3.54 (dt, J = 10.1, 4.7 Hz, 4H), 3.42 (dd,
			J = 5.7, 4.0 Hz, 4H), 2.99 (q, J = 6.5 Hz, 2H), 2.28
			(t, J = 7.5 Hz, 2H), 1.49 (p, J = 7.5 Hz, 2H), 1.38
			(p, J = 7.0 Hz, 2H), 1.26 (td, J = 8.4, 4.3 Hz, 2H).
260	1- neopentyl- piperazine	2.7
			1-(4-chlorobenzyl)-3-(6-(4-neopentylpiperazin-
			1-yl)-6-oxohexyl)urea. LRMS (APCI) m/z 437.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.37
			(d, J = 8.5 Hz, 2H), 7.25 (d, J = 8.4 Hz, 2H), 6.31
			(t, J = 6.1 Hz, 1H), 5.93 (t, J = 5.6 Hz, 1H), 4.18
			(d, J = 6.0 Hz, 2H), 3.40 (d, J = 9.2 Hz, 4H), 2.99
			(q, J = 6.5 Hz, 2H), 2.47-2.36 (m, 4H), 2.26 (t, J =
			7.4 Hz, 2H), 2.05 (s, 2H), 1.47 (p, J = 7.3 Hz,
			2H), 1.37 (p, J = 7.0 Hz, 2H), 1.25 (q, J = 7.9 Hz,
			3H), 0.86 (s, 9H).
261	2-methyl- 1- (piperazin- 1-yl)propan- 2-ol	2.7
			1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-
			methylpropyl)piperazin-1-yl)-6-oxohexyl)urea.
			LRMS (APCI) m/z 439.2 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 9.09 (s, 1H), 7.37 (d, J = 8.4
			Hz, 2H), 7.26 (d, J = 8.4 Hz, 2H), 6.33 (s, 1H),
			5.94 (s, 1H), 4.21 (dd, J = 24.1, 9.6 Hz, 3H), 3.95
			(d, J = 14.5 Hz, 1H), 3.52 (d, J = 13.0 Hz, 4H),
			3.24 (t, J = 12.4 Hz, 1H), 3.13 (d, J = 3.8 Hz, 3H),
			3.03-2.95 (m, 2H), 2.33 (q, J = 7.2 Hz, 2H), 1.50
			(p, J = 7.5 Hz, 2H), 1.39 (p, J = 7.0 Hz, 2H), 1.26
			(s, 8H).
262	o- toluidine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(o-
			tolyl)hexanamide. LRMS (APCI) m/z 388.1
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 9.21
			(s, 1H), 7.36 (d, J = 8.4 Hz, 3H), 7.26 (d, J = 8.4
			Hz, 2H), 7.20 (d, J = 7.5 Hz, 1H), 7.14 (t, J = 7.5
			Hz, 1H), 7.07 (t, J = 7.3 Hz, 1H), 6.32 (t, J = 6.1
			Hz, 1H), 5.95 (t, J = 5.8 Hz, 1H), 4.18 (d, J = 6.0
			Hz, 2H), 3.01 (q, J = 6.5 Hz, 2H), 2.32 (t, J = 7.1
			Hz, 2H), 2.18 (s, 3H), 1.69-1.53 (m, 2H), 1.41
			(q, J = 7.2 Hz, 2H), 1.36-1.25 (m, 2H).
263	pyridin- 4-amine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(pyridin-4-
			yl)hexanamide. LRMS (APCI) m/z 375.0
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.40
			(d, J = 6.4 Hz, 2H), 8.14 (s, 1H), 7.61-7.50 (m,
			2H), 7.36 (d, J = 8.5 Hz, 2H), 7.25 (d, J = 8.4 Hz,
			2H), 6.31 (t, J = 6.1 Hz, 1H), 5.95 (t, J = 5.7 Hz,
			1H), 4.17 (d, J = 6.0 Hz, 2H), 3.17 (d, J = 5.0 Hz,
			1H), 3.00 (q, J = 6.5 Hz, 2H), 2.35 (t, J = 7.4 Hz,
			2H), 1.59 (p, J = 7.5 Hz, 2H), 1.40 (p, J = 7.0 Hz,
			2H), 1.28 (p, J = 7.7 Hz, 2H).
264	N,3- dimethyl aniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(m-
			tolyl)hexanamide. LRMS (APCI) m/z 402.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.40-
			7.29 (m, 3H), 7.24 (d, J = 8.4 Hz, 2H), 7.20-7.06
			(m, 3H), 6.28 (t, J = 6.1 Hz, 1H), 5.89 (d, J = 5.5
			Hz, 1H), 4.16 (d, J = 5.9 Hz, 2H), 3.13 (s, 3H),
			2.93 (q, J = 6.1 Hz, 2H), 2.33 (s, 3H), 2.06-1.93
			(m, 2H), 1.50-1.37 (m, 2H), 1.34-1.20 (m, 2H),
			1.18-1.01 (m, 2H).
265	N- methylpyridin- 4-amine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-
			(pyridin-4-yl)hexanamide. LRMS (APCI) m/z
			389.1 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			8.83-8.45 (m, 2H), 7.42 (d, J = 4.7 Hz, 2H), 7.39-
			7.31 (m, 2H), 7.29-7.20 (m, 2H), 6.30 (t, J =
			6.1 Hz, 1H), 5.91 (t, J = 5.8 Hz, 1H), 4.17 (d, J =
			6.0 Hz, 2H), 3.24 (s, 3H), 2.96 (q, J = 6.6 Hz, 2H),
			2.28 (t, J = 7.4 Hz, 2H), 1.50 (p, J = 7.5 Hz, 2H),
			1.31 (p, J = 7.0 Hz, 2H), 1.26-1.13 (m, 2H).
266	N,2- dimethyl aniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(o-
			tolyl)hexanamide. LRMS (APCI) m/z 402.1
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.39-
			7.33 (m, 3H), 7.31-7.27 (m, 2H), 7.26-7.20 (m,
			3H), 6.28 (t, J = 6.1 Hz, 1H), 5.88 (t, J = 5.7 Hz,
			1H), 4.16 (d, J = 6.1 Hz, 2H), 3.05 (s, 3H), 2.92
			(q, J = 6.6 Hz, 2H), 2.16 (s, 3H), 1.83 (ddt, J =
			55.8, 15.2, 7.3 Hz, 2H), 1.42 (p, J = 7.5 Hz, 2H),
			1.24 (dq, J = 14.4, 6.8 Hz, 2H), 1.09 (ddd, J =
			12.1, 9.1, 5.3 Hz, 2H).
267	N- methyl- 1-(m-tolyl) methanamine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-(3-
			methylbenzyl)hexanamide. LRMS (APCI) m/z
			416.2 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.41-7.31 (m, 2H), 7.31-7.16 (m, 3H), 7.08 (dd,
			J = 12.9, 7.5 Hz, 1H), 7.03-6.90 (m, 2H), 6.40-
			6.24 (m, 1H), 6.00-5.85 (m, 1H), 4.53 (s, 1H),
			4.46 (s, 1H), 4.17 (t, J = 4.6 Hz, 2H), 2.99 (dq, J =
			13.5, 6.1 Hz, 2H), 2.89 (s, 2H), 2.80 (s, 1H), 2.41-
			2.32 (m, 2H), 2.29 (d, J = 7.4 Hz, 3H), 1.52 (dp,
			J = 15.1, 7.4 Hz, 2H), 1.45-1.16 (m, 4H).
268	N- methylaniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-
			phenylhexanamide. LRMS (APCI) m/z 388.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.45 (t,
			J = 7.5 Hz, 2H), 7.33 (dd, J = 17.8, 8.0 Hz, 5H),
			7.24 (d, J = 8.3 Hz, 2H), 6.28 (t, J = 6.1 Hz, 1H),
			5.93-5.79 (m, 1H), 4.16 (d, J = 5.9 Hz, 2H), 3.16
			(d, J = 8.2 Hz, 3H), 2.93 (q, J = 6.5 Hz, 2H), 2.10-
			1.91 (m, 2H), 1.51-1.35 (m, 2H), 1.34-1.18
			(m, 2H), 1.18-1.03 (m, 2H).
269	N- methyl-1- phenylmethanamine	2.7
			N-benzyl-6-(3-(4-chlorobenzyl)ureido)-N-
			methylhexanamide. LRMS (APCI) m/z 402.2
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.43-
			7.29 (m, 4H), 7.26 (dq, J = 7.5, 4.6, 3.0 Hz, 3H),
			7.19 (t, J = 7.1 Hz, 2H), 6.31 (q, J = 6.5 Hz, 1H),
			5.93 (dt, J = 13.1, 5.7 Hz, 1H), 4.57 (s, 1H), 4.50
			(s, 1H), 4.18 (dd, J = 6.1, 3.7 Hz, 2H), 3.06-2.93
			(m, 2H), 2.90 (s, 2H), 2.81 (s, 1H), 2.34 (dt, J =
			16.2, 7.4 Hz, 2H), 1.52 (dp, J = 15.2, 7.5 Hz, 2H),
			1.33 (dddd, J = 31.9, 28.3, 17.2, 7.0 Hz, 4H).
270	N- methylpyridin- 3-amine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-
			(pyridin-3-yl)hexanamide. LRMS (APCI) m/z
			389.1 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			8.62-8.50 (m, 2H), 7.84 (d, J = 8.3 Hz, 1H), 7.51
			(dd, J = 8.1, 4.8 Hz, 1H), 7.36 (d, J = 8.4 Hz, 2H),
			7.24 (d, J = 8.3 Hz, 2H), 6.29 (s, 1H), 5.90 (s, 1H),
			4.17 (d, J = 5.2 Hz, 2H), 3.19 (d, J = 12.0 Hz, 4H),
			2.96 (d, J = 17.7 Hz, 2H), 2.20 (t, J = 7.4 Hz, 1H),
			1.49 (dd, J = 15.0, 7.8 Hz, 2H), 1.36 (q, J = 7.2
			Hz, 1H), 1.27 (t, J = 7.7 Hz, 2H), 1.15 (dt, J =
			13.7, 5.5 Hz, 1H).
271	N- methylpyridin- 2-amine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-methyl-N-
			(pyridin-2-yl)hexanamide. LRMS (APCI) m/z
			389.1 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			8.48 (dd, J = 4.9, 1.8 Hz, 1H), 7.88 (td, J = 7.8, 2.0
			Hz, 1H), 7.48 (d, J = 8.1 Hz, 1H), 7.36 (d, J = 8.3
			Hz, 2H), 7.30 (dd, J = 7.4, 4.9 Hz, 1H), 7.25 (d, J =
			8.2 Hz, 2H), 6.29 (t, J = 6.2 Hz, 1H), 5.90 (t, J =
			5.6 Hz, 1H), 4.17 (d, J = 5.8 Hz, 2H), 3.25 (s, 3H),
			2.95 (q, J = 6.5 Hz, 2H), 2.26 (t, J = 7.4 Hz, 2H),
			1.49 (p, J = 7.4 Hz, 2H), 1.29 (h, J = 8.1, 7.5 Hz,
			2H), 1.18 (q, J = 8.0 Hz, 2H).
272	2- fluoroaniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(2-
			fluorophenyl)hexanamide. LRMS (APCI) m/z
			392.1 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			9.64 (s, 1H), 7.92-7.80 (m, 1H), 7.36 (d, J = 8.3
			Hz, 2H), 7.25 (d, J = 8.4 Hz, 3H), 7.14 (dd, J =
			6.6, 3.4 Hz, 2H), 6.32 (t, J = 6.1 Hz, 1H), 5.96 (t, J =
			5.7 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H), 3.01 (q, J =
			6.6 Hz, 2H), 2.37 (t, J = 7.4 Hz, 2H), 1.59 (p, J =
			7.4 Hz, 2H), 1.41 (p, J = 6.9 Hz, 2H), 1.30 (h, J =
			7.5, 6.3 Hz, 2H).
273	[1,1′- biphenyl]-2- amine	2.7
			N-([1,1′-biphenyl]-2-yl)-6-(3-(4-
			chlorobenzyl)ureido)hexanamide. LRMS
			(APCI) m/z 450.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 9.17 (s, 1H), 7.43 (t, J = 8.0 Hz, 3H),
			7.40-7.22 (m, 10H), 6.31 (t, J = 6.0 Hz, 1H),
			5.93 (t, J = 5.7 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H),
			2.98 (q, J = 6.6 Hz, 2H) 2.14 (t, J = 7.3 Hz, 2H),
			1.47 (t, J = 7.6 Hz, 2H), 1.41-1.29 (m, 2H), 1.24-
			1.14 (m, 2H).
274	2-fluoro- N-methylaniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(2-
			fluorophenyl)-N-methylhexanamide. LRMS
			(APCI) m/z 406.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.46 (dt, J = 20.7, 10.4 Hz, 2H), 7.35
			(d, J = 8.2 Hz, 3H), 7.33-7.18 (m, 3H), 6.28 (s,
			1H), 5.89 (d, J = 6.1 Hz, 1H), 4.16 (d, J = 5.7 Hz,
			2H), 3.11 (s, 3H), 2.92 (d, J = 6.1 Hz, 2H), 2.06-
			1.85 (m, 2H), 1.43 (p, J = 7.5 Hz, 2H), 1.24 (q, J =
			7.4 Hz, 2H), 1.12 (q, J = 7.8 Hz, 2H).
278	6- methylpyridin- 3-amine	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(6-
			methylpyridin-3-yl)hexanamide. LRMS (APCI)
			m/z 389.0 (M + H). 1H NMR (400 MHz, DMSO-
			d6) δ 9.97 (s, 1H), 8.59 (d, J = 2.5 Hz, 1H), 7.91
			(dd, J = 8.6, 2.6 Hz, 1H), 7.36 (d, J = 8.1 Hz, 2H),
			7.25 (d, J = 8.1 Hz, 2H), 7.17 (d, J = 8.4 Hz, 1H),
			6.31 (t, J = 6.1 Hz, 1H), 5.95 (t, J = 5.8 Hz, 1H),
			4.17 (d, J = 6.1 Hz, 2H), 3.00 (q, J = 6.5 Hz, 2H),
			2.40 (s, 3H), 2.31 (t, J = 7.5 Hz, 2H), 1.59 (p, J =
			7.5 Hz, 2H), 1.40 (p, J = 7.0 Hz, 2H), 1.35-1.22
			(m, 2H).
284	4- fluoroaniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(4-
			fluorophenyl)hexanamide. LRMS (APCI) m/z
			392.0 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			9.91 (s, 1H), 7.60 (t, J = 7.2 Hz, 2H), 7.42-7.30
			(m, 2H), 7.25 (d, J = 7.2 Hz, 2H), 7.12 (t, J = 8.7
			Hz, 2H), 6.31 (s, 1H), 5.95 (s, 1H), 4.25-4.09 (m,
			2H), 3.00 (d, J = 6.7 Hz, 2H), 2.29 (t, J = 7.5 Hz,
			2H), 1.65-1.52 (m, 2H), 1.49-1.34 (m, 2H),
			1.34-1.19 (m, 2H).
285	3- fluoroaniline	2.7
			6-(3-(4-chlorobenzyl)ureido)-N-(3-
			fluorophenyl)hexanamide. LRMS (APCI) m/z
			391.9 (M + H). 1H NMR (400 MHz, DMSO-d6) δ
			10.08 (s, 1H), 7.61 (dd, J = 12.0, 2.3 Hz, 1H), 7.36
			(d, J = 7.4 Hz, 2H), 7.34-7.22 (m, 4H), 6.85 (t, J =
			8.5 Hz, 1H), 6.31 (d, J = 6.8 Hz, 1H), 5.95 (s,
			1H), 4.17 (d, J = 5.8 Hz, 2H), 3.00 (q, J = 5.9 Hz,
			2H), 2.31 (t, J = 7.4 Hz, 2H), 1.59 (p, J = 7.6 Hz,
			2H), 1.39 (q, J = 7.3 Hz, 2H), 1.29 (q, J = 7.8 Hz,
			2H).

Example 3

Preparation of 1-(2-((2-chlorophenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea (Compound 116)

1-(2-((2-chlorophenyl)sulfonyl)-2-azaspiro[3.3]heptan-6-yl)-3-(4-methoxybenzyl)urea. 2-Chlorobenzenesulfonyl chloride (114 mg, 0.544 mmol, 1.5 equiv) was added to a stirring solution of 1-(4-methoxybenzyl)-3-(2-azaspiro[3.3]heptan-6-yl)urea (100 mg, 0.363 mmol, 1 equiv) and NEt₃ (147 μL, 0.770 mmol, 3 equiv) in DMF (1 mL) at rt. After 2 h, the reaction was diluted with MeOH to a total volume of 1.8 mL, filtered through a 0.4 μm syringe filter, and product isolated by reverse phase HPLC (0->70% MeCN/H2O w/0.1% formic acid) as a white solid (21 mg, 18%). LRMS (APCI) m/z 450 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.97 (dt, J=8.0, 1.8 Hz, 1H), 7.76-7.68 (m, 2H), 7.59 (t, J=7.4 Hz, 1H), 7.13 (d, J=8.3 Hz, 2H), 6.86 (d, J=8.5 Hz, 2H), 6.17 (t, J=5.9 Hz, 1H), 6.12 (d, J=7.9 Hz, 1H), 4.10 (dd, J=16.2, 6.9 Hz, 2H), 3.97 (s, 1H), 3.94 (s, 2H), 3.87 (s, 1H), 3.83 (s, 1H), 3.72 (s, 2H), 2.48-2.38 (m, 1H), 2.33 (ddd, J=10.2, 7.7, 3.0 Hz, 2H), 2.27-2.15 (m, 1H), 1.93 (td, J=8.9, 3.0 Hz, 1H).

Compounds in the following table were prepared in a similar manner as Compound 116, using the intermediates and reagents as listed.

Compound
No.	Amine	Intermediate	Structure, Name and Data
117	(2- chlorophe- nyl)meth- anesulfonyl chloride	3.2
			1-(2-((2-chlorobenzyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			464 (M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.60 - 7.47 (m, 2H), 7.40 (dd, J = 6.6, 3.2
			Hz, 2H), 7.15 (d, J = 8.3 Hz, 2H), 6.87 (d, J =
			8.5 Hz, 2H), 6.19 (t, J = 6.0 Hz, 1H), 6.14 (d,
			J = 7.8 Hz, 1H), 4.59 (s, 2H), 4.10 (d, J = 5.9
			Hz, 2H), 4.00 - 3.91 (m, 1H), 3.89 (s, 2H),
			3.79 (s, 2H), 3.73 (s, 3H), 2.44 (t, J = 10.0 Hz,
			2H), 1.98 (t, J = 10.4 Hz, 2H).
118	2-(2- chlorophe- nyl)ethane- 1- sulfonyl chloride	3.2
			1-(2-((2-chlorophenethyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			478 (M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.53 - 7.43 (m, 2H), 7.37 - 7.24 (m, 2H),
			7.15 (d, J = 8.3 Hz, 2H), 6.86 (d, J = 8.4 Hz,
			2H), 6.16 (dd, J = 16.5, 7.0 Hz, 2H), 4.09 (d, J =
			5.9 Hz, 2H), 3.91 (s, 3H), 3.80 (s, 2H), 3.72
			(d, J = 0.8 Hz, 3H), 3.37 (d, J = 7.9 Hz, 2H),
			3.16 - 3.01 (m, 2H), 2.43 (t, J = 10.1 Hz, 2H),
			1.97 (dd, J = 12.0, 8.7 Hz, 2H).
130	(1S,4R)- bicyclo[2.2.1] heptane- 2- sulfonyl chloride	3.2
			1-(2-(bicyclo[2.2.1]heptan-2-ylsulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			434 (M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.07 (d, J = 8.3 Hz, 2H), 6.79 (d, J = 8.3 Hz,
			2H), 6.14 - 6.01 (m, 2H), 4.02 (d, J = 5.9 Hz,
			2H), 3.86 (q, J = 8.0 Hz, 1H), 3.78 (s, 2H),
			3.67 (d, J = 2.7 Hz, 2H), 3.65 (s, 3H), 3.00
			(dd, J = 8.8, 5.9 Hz, 1H), 2.46 (s, 1H), 2.35 (t,
			J = 10.0 Hz, 2H), 2.23 (s, 1H), 1.90 (dd, J =
			12.2, 8.7 Hz, 2H), 1.65 (d, J = 12.7 Hz, 1H),
			1.54 (d, J = 9.4 Hz, 2H), 1.44 (d, J = 9.8 Hz,
			2H), 1.22 (t, J = 9.3 Hz, 1H), 1.14-0.99 (m,
			2H).
131	methyl 4- (chlorosul- fonyl)cyclo- hexane- 1- carboxylate	3.2
			methyl 4-((6-(3-(4-methoxybenzyl)ureido)-
			2-azaspiro[3.3]heptan-2-
			yl)sulfonyl)cyclohexane-1-carboxylate.
			LRMS (APCI) m/z 480 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 7.15 (d, J = 8.3 Hz,
			2H), 6.87 (d, J = 8.5 Hz, 2H), 6.24 - 6.05 (m,
			2H), 4.09 (d, J = 5.9 Hz, 2H), 3.94 (h, J = 8.1
			Hz, 1H), 3.80 (s, 2H), 3.72 (s, 3H), 3.69 (s,
			2H), 3.62 (s, 3H), 3.49 (dt, J = 12.6, 3.9 Hz,
			2H), 2.84 (td, J = 12.0, 2.7 Hz, 3H), 2.42
			(ddd, J = 10.1, 7.7, 3.0 Hz, 2H), 1.97 (td, J =
			8.9, 3.0 Hz, 2H), 1.88 (dd, J = 13.7, 3.6 Hz,
			2H), 1.52 (qd, J = 11.5, 4.1 Hz, 3H).
120	phenylmeth- anesulfo- nyl chloride	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-2-yl)-
			1-(2-chlorophenyl)methanesulfonamide.
			LRMS (APCI) m/z 482 (M + H). 1H NMR
			(400 MHz, Methanol-d4) δ 7.59 - 7.53 (m,
			1H), 7.51 - 7.45 (m, 1H), 7.41 -7.34 (m,
			2H), 7.34 - 7.23 (m, 4H), 4.48 (s, 2H), 4.28
			(s, 2H), 4.01 (p, J = 8.0 Hz, 1H), 3.62 (p, J =
			8.3 Hz, 1H), 2.38 (ddd, J = 13.0, 10.9, 5.4 Hz,
			2H), 2.22 (dddd, J = 25.0, 12.4, 7.6, 5.5 Hz,
			2H), 1.99 (td, J = 11.6, 9.0 Hz, 2H), 1.85 (dd,
			J = 11.1, 8.6 Hz, 2H).
121	benzenesul- fonyl chloride	3.4
			1-(2-((2-chlorophenyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)-3-(4-
			methoxybenzyl)urea. LRMS (APCI) m/z
			434 (M + H). 1H NMR (400 MHz, DMSO-d6)
			δ 7.88 (d, J = 8.6 Hz, 1H), 7.78 (dd, J = 7.0,
			1.8 Hz, 2H), 7.65 - 7.55 (m, 3H), 7.38 - 7.28
			(m, 3H), 7.24 - 7.18 (m, 2H), 6.23 (s, 1H),
			6.12 (s, 1H), 4.13 (s, 2H), 3.50 (q, J = 8.1 Hz,
			1H), 2.22 (dt, J = 11.8, 6.1 Hz, 1H), 2.12 -
			1.97 (m, 3H), 1.87 (dt, J = 12.2, 6.7 Hz, 1H),
			1.79 - 1.63 (m, 3H). LRMS (APCI) m/z 434
			(M + H).
213	pyridine- 3-sulfonyl chloride	3.4
			N-(6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-2-
			yl)pyridine-3-sulfonamide. LRMS (APCI)
			m/z 435 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.93 (d, J = 2.3 Hz, 1H), 8.82 (d,
			J = 4.8 Hz, 1H), 8.14 (t, J = 8.5 Hz, 2H), 7.64
			(dd, J = 8.0, 4.9 Hz, 1H), 7.35 (d, J = 8.2 Hz,
			2H), 7.22 (d, J = 8.2 Hz, 2H), 6.23 (t, J = 6.1
			Hz, 1H), 6.12 (d, J = 8.0 Hz, 1H), 4.13 (d, J =
			5.9 Hz, 2H), 3.83 (q, J = 8.0 Hz, 1H), 3.57 (q,
			J = 8.1 Hz, 1H), 2.31 - 2.19 (m, 1H), 2.16 -
			2.00 (m, 2H), 1.91 (dt, J = 12.1, 6.3 Hz, 1H),
			1.71 (p, J = 9.5 Hz, 4H).
216	2- chloroben- zenesulfonyl chloride	3.1
			1-(4-chlorobenzyl)-3-(2-((2-
			chlorophenyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 454 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.96 (dd, J = 7.9, 1.5 Hz, 1H),
			7.77 - 7.66 (m, 2H), 7.58 (ddd, J = 8.5, 6.9,
			1.8 Hz, 1H), 7.39 - 7.31 (m, 2H), 7.25- 7.20
			(m, 2H), 6.30 (t, J = 6.1 Hz, 1H), 6.21 (d, J =
			7.9 Hz, 1H), 4.14 (d, J = 6.0 Hz, 2H), 4.09 (q,
			J = 5.3 Hz, 1H), 3.93 (s, 2H), 3.83 (s, 2H),
			2.33 (ddd, J = 10.1, 7.6, 3.0 Hz, 2H), 1.94 (td,
			J = 8.9, 3.0 Hz, 2H).
217	3- chloroben- zenesulfonyl chloride	3.1
			1-(4-chlorobenzyl)-3-(2-((3-
			chlorophenyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 454 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.87 (dt, J = 8.0, 1.5 Hz, 1H),
			7.83 - 7.77 (m, 2H), 7.73 (t, J = 7.8 Hz, 1H),
			7.39 - 7.32 (m, 2H), 7.25 - 7.18 (m, 2H), 6.27
			(t, J = 6.1 Hz, 1H), 6.15 (d, J = 7.8 Hz, 1H),
			4.12 (d, J = 6.0 Hz, 2H), 3.88 - 3.74 (m,3H),
			3.67 (s, 2H), 2.13 (ddd, J = 10.1, 7.6, 3.0 Hz,
			2H), 1.80 (td, J = 8.9, 3.0 Hz, 2H).
218	2- methoxy- benzenesul- fonyl chloride	3.1
			1-(4-chlorobenzyl)-3-(2-((2-
			methoxyphenyl)sulfonyl)-2-
			azaspiro[3.3]heptan-6-yl)urea. LRMS
			(APCI) m/z 450 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.72 (dd, J = 7.8, 1.7 Hz, 1H),
			7.67 (ddd, J = 8.8, 7.4, 1.8 Hz, 1H), 7.37 -
			7.33 (m, 2H), 7.29 (d, J = 8.4 Hz, 1H), 7.25-
			7.20 (m, 2H), 7.12 (td, J = 7.6, 1.0Hz,1H),
			6.29 (t, J = 6.1 Hz, 1H), 6.19 (d, J = 7.9 Hz,
			1H), 4.14 (d, J = 6.0 Hz, 2H), 4.09 (q, J = 5.4
			Hz, 1H), 3.91 (s, 3H), 3.86 (s, 2H), 3.76 (s,
			2H), 2.28 (ddd, J = 10.1, 7.7, 3.0 Hz, 2H),
			1.90 (td, J = 8.9, 3.0 Hz, 2H).

Example 4

Preparation of tert-butyl 1-((3-(4-chlorobenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate (Compound 27)

Step 1. tert-butyl 1-((3-(4-chlorobenzyl)ureido)methyl)-6-azaspiro[2.5]octane-6-carboxylate.

To a room temperature solution of N,N′-disuccinimidyl carbonate (0.160 mg, 0.62 mmol, 1.0 equiv) in acetonitrile (10 mL) was added tert-butyl 1-(aminomethyl)-6-azaspiro[2.5]octane-6-carboxylate (0.15 g, 0.62 mmol, 1.0 equiv) followed by pyridine (0.06 mL, 0.62 mmol, 1.0 equiv) in a dropwise fashion. After 20 minutes, a solution 4-chloro benzyl amine (88 mg, 0.62 mmol, 1.0 equiv) in acetonitrile (2 mL) was added followed by N,N-diisopropylethylamine (0.11 mL, 1.24 mmol, 2.0 equiv). The resulting mixture was stirred at room temperature for approximately one hour then concentrated to dryness. Resultant mixture was diluted with ethyl acetate (50 mL) and extracted with water (2×15 mL) and brine (1×15 mL). The organic phase was dried to a viscous oil which was purified by reverse phase chromatography and afforded the desired product as a white foam (148 mg, 0.36 mmol, 58.1% yield). LCMS-APCI (POS.) m/z: 308 (M-Boc+H)⁺. 1H NMR (400 MHz, DMSO-d₆) δ 7.45-7.32 (m, 2H), 7.25 (d, J=8.5 Hz, 2H), 6.37 (t, J=6.1 Hz, 1H), 5.94 (t, J=5.4 Hz, 1H), 4.18 (d, J=6.0 Hz, 2H), 3.43 (dddd, J=19.2, 12.7, 6.6, 3.8 Hz, 2H), 3.17 (dt, J=13.8, 5.9 Hz, 3H), 2.90 (ddd, J=13.7, 8.5, 5.2 Hz, 1H), 1.51 (ddd, J=12.3, 10.2, 6.2 Hz, 1H), 1.40 (s, 9H), 1.31 (ddd, J=17.2, 7.1, 3.5 Hz, 2H), 1.14 (ddd, J=13.1, 6.5, 3.3 Hz, 1H), 0.79 (tt, J=8.5, 6.2 Hz, 1H), 0.45 (dd, J=8.5, 4.3 Hz, 1H), 0.16 (t, J=4.8 Hz, 1H).

Compounds in the following table were prepared in a similar manner as Compound 27, using the intermediates and reagents as listed.

Compound
No.	Reagent I	Reagent II	Structure, Name and Data
2	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	4- (aminomethyl) benzamide	tert-butyl (6-(3-(4- carbamoylbenzyl)ureido)spiro[3.3]heptan- 2-yl)carbamate. LCMS-ESI (POS.) m/z: 303 (M-Boc + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.90 (s, 1H), 7.85- 7.75 (m, 2H), 7.38-7.19 (m, 3H), 7.04 (d, J = 8.1 Hz, 1H), 6.27 (t, J = 6.0 Hz, 1H), 6.18 (d, J = 8.1 Hz, 1H), 4.21 (d, J = 5.9 Hz, 2H), 3.92 (h, J = 8.2 Hz, 1H), 3.79 (h, J = 8.2 Hz, 1H), 2.38-2.18 (m, 2H), 2.18-1.98 (m, 2H), 1.92-1.81 (m, 2H), 1.77 (ddd, J = 13.8, 10.4, 8.6 Hz, 2H), 1.36 (s, 9H).
3	4,4- dimethyl- cyclohexan-1- amine	4- (aminomethyl) benzamide	4-((3-(4,4- dimethylcyclohexyl)ureido)methyl)benzamide. LCMS-ESI (POS.) m/z: 304 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.92 (s, 1H), 7.86-7.67 (m, 2H), 7.39- 7.20 (m, 3H), 6.32 (t, J = 6.1 Hz, 1H), 5.95 (d, J = 8.0 Hz, 1H), 4.23 (d, J = 6.0 Hz, 2H), 1.70-1.56 (m, 2H), 1.39-1.09 (m, 7H), 0.89 (s, 6H).
4	3- phenylcyclo- butan-1-amine	4- (aminomethyl) benzamide	4-((3-(3- phenylcyclobutyl)ureido)methyl)benzamide. LCMS-ESI (POS.) m/z: 324 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.91 (s, 1H), 7.86-7.73 (m, 2H), 7.41- 7.25 (m, 7H), 7.23-7.11 (m, 1H), 6.48 (d, J = 7.4 Hz, 1H), 6.37 (t, J = 6.1 Hz, 1H), 4.25 (d, J = 6.0 Hz, 2H), 4.22-4.15 (m, 1H), 3.48 (tt, J = 9.7, 5.5 Hz, 1H), 2.44- 2.22 (m, 4H).
5	tert-butyl 4- amino- piperidine-1- carboxylate	4- (aminomethyl) benzamide	tert-butyl 4-(3-(4- carbamoylbenzyl)ureido)piperidine-1- carboxylate. LCMS-ESI (POS.) m/z: 277 (M-Boc + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.91 (s, 1H), 7.86-7.69 (m, 2H), 7.30 (dd, J = 8.6, 2.1 Hz, 3H), 6.30 (t, J = 6.0 Hz, 1H), 6.11-5.93 (m, 1H), 4.24 (d, J = 6.0 Hz, 2H), 3.80 (d, J = 13.3 Hz, 2H), 3.62-3.47 (m, 1H), 2.85 (s, 2H), 1.74 (dd, J = 12.7, 3.8 Hz, 2H), 1.40 (s, 9H), 1.29-1.08 (m, 2H).
6	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	pyridin-4- ylmethanamine	tert-butyl (6-(3-(pyridin-4- ylmethyl)ureido)spiro[3.3]heptan-2- yl)carbamate. LCMS-ESI (POS.) m/z: 361 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 8.47 (d, J = 5.4 Hz, 2H), 7.21 (d, J = 4.9 Hz, 2H), 7.04 (d, J = 8.0 Hz, 1H), 6.37 (t, J = 6.2 Hz, 1H), 6.30 (d, J = 8.0 Hz, 1H), 4.20 (d, J = 6.0 Hz, 2H), 3.92 (h, J = 8.1 Hz, 1H), 3.80 (h, J = 8.1 Hz, 1H), 2.28 (ddq, J = 22.9, 11.0, 6.0, 5.6 Hz, 2H), 2.18-2.00 (m, 2H), 1.95-1.70 (m, 4H), 1.36 (s, 9H).
7	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	4-methoxy benzyl amine	tert-butyl (6-(3-(4- methoxybenzyl)ureido)spiro[3.3]heptan- 2-yl)carbamate. LCMS-ESI (POS.) m/z: 390 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.15 (d, J = 8.3 Hz, 2H), 7.04 (d, J = 8.1 Hz, 1H), 6.86 (d, J = 8.4 Hz, 2H), 6.17-5.99 (m, 2H), 4.09 (d, J = 5.8 Hz, 2H), 3.92 (h, J = 8.2 Hz, 1H), 3.79 (q, J = 8.1 Hz, 1H), 3.72 (s, 3H), 2.27 (qd, J = 11.4, 5.2 Hz, 2H), 2.17-2.00 (m, 2H), 1.86 (q, J = 10.1 Hz, 2H), 1.82-1.68 (m, 2H), 1.36 (s, 9H).
8	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	4-chloro benzyl amine	tert-butyl (6-(3-(4- chlorobenzyl)ureido)spiro[3.3]heptan- 2-yl)carbamate. LCMS-ESI (POS.) m/z: 291 (M-Boc + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.36 (d, J = 8.1 Hz, 2H), 7.24 (d, J = 8.1 Hz, 2H), 7.04 (d, J = 8.3 Hz, 1H), 6.27 (t, J = 6.1 Hz, 1H), 6.19 (d, J = 8.0 Hz, 1H), 4.15 (d, J = 6.0 Hz, 2H), 3.92 (dq, J = 17.8, 9.1, 8.7 Hz, 1H), 3.84- 3.70 (m, 1H), 2.28 (ddd, J = 25.2, 14.4, 8.3 Hz, 2H), 2.09 (td, J = 15.1, 13.6, 5.8 Hz, 2H), 1.92-1.65 (m, 4H), 1.36 (s, 9H).
9	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	(4- (aminomethyl) phenyl)methanol	tert-butyl (6-(3-(4- (hydroxymethyl)benzyl)ureido)spiro[3.3] heptan-2-yl)carbamate. LCMS-ESI (POS.) m/z: 390 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.24 (d, J = 7.8 Hz, 2H), 7.17 (d, J = 7.8 Hz, 2H), 7.04 (d, J = 8.0 Hz, 1H), 6.17 (t, J = 6.0 Hz, 1H), 6.12 (d, J = 8.0 Hz, 1H), 5.12 (t, J = 5.7 Hz, 1H), 4.46 (d, J = 5.0 Hz, 2H), 4.15 (d, J = 5.9 Hz, 2H), 3.93 (h, J = 8.0 Hz, 1H), 3.80 (p, J = 7.9 Hz, 1H), 2.27 (dt, J = 12.5, 5.6 Hz, 2H), 2.18-1.99 (m, 2H), 1.86 (q, J = 9.9 Hz, 2H), 1.80-1.65 (m, 2H), 1.36 (s, 9H).
10	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	(1H-pyrazol- 4- yl)methanamine	tert-butyl (6-(3-((1H-pyrazol-4- yl)methyl)ureido)spiro[3.3]heptan-2- yl)carbamate. LCMS-ESI (POS.) m/z: 350 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 12.56 (br s, 1H), 7.58-7.34 (m, 2H), 7.04 (d, J = 8.1 Hz, 1H), 6.02 (d, J = 8.1 Hz, 1H), 5.89 (t, J = 5.6 Hz, 1H), 4.01 (d, J = 5.5 Hz, 2H), 3.91 (h, J = 8.1 Hz, 1H), 3.78 (p, J = 8.0 Hz, 1H), 2.27 (qd, J = 11.2, 10.0, 5.5 Hz, 2H), 2.08 (tt, J = 12.6, 5.7 Hz, 2H), 1.85 (q, J = 10.5 Hz, 2H), 1.79-1.66 (m, 2H), 1.36 (s, 9H).
11	tert-butyl (6- aminospiro[3.3] heptan-2- yl)carbamate	oxazol-5- ylmethanamine	tert-butyl (6-(3-(oxazol-5- ylmethyl)ureido)spiro[3.3]heptan-2- yl)carbamate. LCMS-ESI (POS.) m/z: 351 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 8.25 (s, 1H), 7.04 (d, J = 8.0 Hz, 1H), 6.92 (s, 1H), 6.29-6.12 (m, 2H), 4.23 (d, J = 5.8 Hz, 2H), 3.91 (h, J = 8.1 Hz, 1H), 3.79 (q, J = 8.2 Hz, 1H), 2.27 (qt, J = 10.8, 5.6 Hz, 2H), 2.17-2.01 (m, 2H), 1.86 (q, J = 10.0 Hz, 2H), 1.82-1.68 (m, 2H), 1.36 (s, 9H).
12	tert-butyl (4- aminocyclohexyl) carbamate	4- (aminomethyl) benzamide	tert-butyl (4-(3-(4- carbamoylbenzyl)ureido)cyclohexyl) carbamate. LCMS-ESI (POS.) m/z: 291 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 7.91 (s, 1H), 7.82 (d, J = 8.1 Hz, 2H), 7.30 (d, J = 7.6 Hz, 3H), 6.73 (dd, J = 25.4, 7.3 Hz, 1H), 6.36 (t, J = 6.0 Hz, 1H), 5.89 (d, J = 7.4 Hz, 1H), 4.25 (d, J = 5.9 Hz, 2H), 3.54 (s, 1H), 3.17 (s, 1H), 1.85-1.68 (m, 1H), 1.62-1.43 (m, 6H), 1.39 (s, 9H), 1.25-1.08 (m, 1H).
25	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	pyridin-4- ylmethanamine	tert-butyl 1-((3-(pyridin-4- ylmethyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 375 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.45-7.32 (m, 2H), 7.25 (d, J = 8.5 Hz, 2H), 6.37 (t, J = 6.1 Hz, 1H), 5.94 (t, J = 5.4 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H), 3.43 (dddd, J = 19.2, 12.7, 6.6, 3.8 Hz, 2H), 3.17 (dt, J = 13.8, 5.9 Hz, 3H), 2.90 (ddd, J = 13.7, 8.5, 5.2 Hz, 1H), 1.51 (ddd, J = 12.3, 10.2, 6.2 Hz, 1H), 1.40 (s, 9H), 1.31 (ddd, J = 17.2, 7.1, 3.5 Hz, 2H), 1.14 (ddd, J = 13.1, 6.5, 3.3 Hz, 1H), 0.79 (tt, J = 8.5, 6.2 Hz, 1H), 0.45 (dd, J = 8.5, 4.3 Hz, 1H), 0.16 (t, J = 4.8 Hz, 1H).
28	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	4-methoxy benzyl amine	tert-butyl 1-((3-(4- methoxybenzyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 304 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 7.23-7.05 (m, 2H), 6.93-6.78 (m, 2H), 6.25 (t, J = 5.9 Hz, 1H), 5.87 (t, J = 5.4 Hz, 1H), 4.12 (d, J = 5.9 Hz, 2H), 3.72 (s, 3H), 3.44 (dddd, J = 19.4, 12.7, 6.6, 3.8 Hz, 2H), 3.19 (tq, J = 13.6, 11.6, 6.1, 4.8 Hz, 3H), 2.88 (ddd, J = 13.7, 8.5, 5.1 Hz, 1H), 1.59-1.44 (m, 1H), 1.39 (s, 9H), 1.31 (ddt, J = 12.8, 8.6, 3.3 Hz, 2H), 1.13 (ddd, J = 13.1, 6.5, 3.5 Hz, 1H), 0.78 (tt, J = 8.4, 5.9 Hz, 1H), 0.45 (dd, J = 8.5, 4.3 Hz, 1H), 0.15 (t, J = 4.8 Hz, 1H).
29	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	(4- (aminomethyl) phenyl)methanol	tert-butyl 1-((3-(4- (hydroxymethyl)benzyl)ureido)methyl)- 6-azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 304 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 7.24 (d, J = 8.0 Hz, 2H), 7.18 (d, J = 8.0 Hz, 2H), 6.30 (t, J = 6.0 Hz, 1H), 5.90 (t, J = 5.4 Hz, 1H), 5.12 (s,1H), 4.45 (s, 2H), 4.17 (d, J = 5.9 Hz, 2H), 3.44 (dddd, J = 19.6, 12.7, 6.6, 3.8 Hz, 2H), 3.26- 3.08 (m, 3H), 2.89 (ddd, J = 13.7, 8.5, 5.1 Hz, 1H), 1.57-1.44 (m, 1H), 1.40 (s, 9H), 1.35-1.25 (m, 2H), 1.13 (ddd, J = 13.1, 6.5, 3.4 Hz, 1H), 0.79 (tt, J = 8.4, 5.8 Hz, 1H), 0.45 (dd, J = 8.6, 4.3 Hz, 1H), 0.16 (t, J = 4.8 Hz, 1H).
30	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	oxazol-5- ylmethanamine	tert-butyl 1-((3-(oxazol-5- ylmethyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 265 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 8.24 (s, 1H), 6.92 (s, 1H), 6.35 (t, J = 5.9 Hz, 1H), 5.96 (t, J = 5.4 Hz, 1H), 4.26 (dd, J = 5.9, 0.9 Hz, 2H), 3.44 (dddd, J = 15.8, 12.8, 6.6, 3.8 Hz, 2H), 3.28-3.07 (m, 3H), 2.89 (ddd, J = 13.7, 8.4, 5.1 Hz, 1H), 1.59-1.44 (m, 1H), 1.39 (s, 9H), 1.31 (ddd, J = 13.2, 5.6, 3.1 Hz, 2H), 1.12 (ddd, J = 13.1, 6.5, 3.5 Hz, 1H), 0.77 (tt, J = 8.3, 5.8 Hz, 1H), 0.44 (dd, J = 8.5, 4.3 Hz, 1H), 0.15 (t, J = 4.9 Hz, 1H).
31	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	(1H-pyrazol- 4- yl)methanamine	tert-butyl 1-((3-((1H-pyrazol-4- yl)methyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 364 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 12.55 (s, 1H), 7.47 (s, 2H), 6.01 (t, J = 5.5 Hz, 1H), 5.77 (t, J = 5.4 Hz, 1H), 4.04 (d, J = 5.4 Hz, 2H), 3.45 (tdd, J = 17.5, 6.5, 3.8 Hz, 2H), 3.25-3.10 (m, 3H), 2.87 (ddd, J = 13.6, 8.4, 5.0 Hz, 1H), 1.50 (ddd, J = 12.5, 8.8, 4.2 Hz, 1H), 1.40 (s, 9H), 1.35-1.28 (m, 2H), 1.12 (ddd, J = 12.9, 6.5, 3.4 Hz, 1H), 0.84-0.69 (m, 1H), 0.44 (dd, J = 8.5, 4.3 Hz, 1H), 0.15 (t, J = 4.8 Hz, 1H).
32	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	N-(4- (aminomethyl) phenyl)acetamide	tert-butyl 1-((3-(4- acetamidobenzyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 331 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 9.87 (s, 1H), 7.57-7.36 (m, 2H), 7.22-7.05 (m, 2H), 6.24 (t, J = 5.9 Hz, 1H), 5.85 (t, J = 5.4 Hz, 1H), 4.13 (d, J = 5.8 Hz, 2H), 3.44 (dddd, J = 18.7, 12.6, 6.5, 3.7 Hz, 2H), 3.20 (tdd, J = 13.5, 10.3, 4.9 Hz, 3H), 2.89 (ddd, J = 13.6, 8.4, 5.1 Hz, 1H), 2.02 (s, 3H), 1.50 (ddd, J = 12.5, 8.2, 3.7 Hz, 1H), 1.39 (s, 9H), 1.32 (ddd, J = 12.6, 7.5, 3.7 Hz, 2H), 1.13 (ddd, J = 12.9, 6.4, 3.5 Hz, 1H), 0.79 (tt, J = 8.2, 5.8 Hz, 1H), 0.45 (dd, J = 8.5, 4.3 Hz, 1H), 0.16 (t, J = 4.8 Hz, 1H).
33	tert-butyl 1- (aminomethyl)- 6- azaspiro[2.5] octane-6- carboxylate	4- (aminomethyl) benzamide	tert-butyl 1-((3-(4- carbamoylbenzyl)ureido)methyl)-6- azaspiro[2.5]octane-6-carboxylate. LCMS-ESI (POS.) m/z: 317 (M-Boc + H)+. 1H NMR (400 MHz, DMSO- d6) δ 7.90 (s, 1H), 7.84-7.73 (m, 2H), 7.39-7.20 (m, 3H), 6.39 (t, J = 6.0 Hz, 1H), 5.95 (t, J = 5.4 Hz, 1H), 4.24 (d, J = 6.0 Hz, 2H), 3.45 (dddd, J = 19.1, 12.6, 5.9, 3.2 Hz, 2H), 3.26-3.09 (m, 3H), 2.91 (ddd, J = 13.6, 8.4, 5.1 Hz, 1H), 1.52 (ddd, J = 17.3, 7.6, 3.6 Hz, 1H), 1.40 (s, 9H), 1.32 (ddd, J = 12.6, 7.5, 3.7 Hz, 2H), 1.14 (ddd, J = 13.0, 6.5, 3.4 Hz, 1H), 0.80 (tt, J = 8.3, 5.8 Hz, 1H), 0.45 (dd, J = 8.5, 4.3 Hz, 1H), 0.16 (q, J = 5.7, 5.3 Hz, 1H).
206	8.1	(4- chlorophenyl) methanamine	1-(4-chlorobenzyl)-3-(2-(4- methylbenzoyl)-2-azaspiro[3.3]heptan- 6-yl)urea. LCMS-ESI (POS.) m/z: 398 (M + H)+. 1H NMR (400 MHz, Methanol- d4) δ 7.43 (t, J = 6.9 Hz, 2H), 7.25-7.09 (m, 6H), 4.49 (s, 2H), 4.30 (s, 1H), 4.17 (s, 3H), 4.10 (s, 1H), 4.03-3.87 (m, 2H), 2.59-2.41 (m, 1H), 2.29 (s, 3H), 2.01 (td, J = 9.4, 8.9, 4.3 Hz, 1H).
207	8.1	(4- fluorophenyl) methanamine	1-(4-fluorobenzyl)-3-(2-(4- methylbenzoyl)-2-azaspiro[3.3]heptan- 6-yl)urea. LCMS-ESI (POS.) m/z: 382 (M + H). 1H NMR (400 MHz, Methanol- d4) δ 7.42 (t, J = 7.0 Hz, 2H), 7.17 (td, J = 5.5, 2.3 Hz, 4H), 6.92 (t, J = 8.6 Hz, 2H), 4.30 (s, 1H), 4.16 (d, J = 4.0 Hz, 3H), 4.09 (s, 1H), 4.02-3.86 (m, 2H), 2.57-2.43 (m, 2H), 2.28 (s, 3H), 2.00 (td, J = 9.3, 8.8, 4.1 Hz, 2H).
210	8.1	pyridin-4- ylmethanamine	1-(2-(4-methylbenzoyl)-2- azaspiro[3.3]heptan-6-yl)-3-(pyridin-4- ylmethyl)urea. LCMS-ESI (POS.) m/z: 365 (M + H)+. 1H NMR (400 MHz, Methanol-d4) δ 8.35 (d, J = 5.2 Hz, 2H), 7.42 (dd, J = 7.8, 4.9 Hz, 2H), 7.25 (d, J = 5.9 Hz, 2H), 7.17 (d, J = 7.7 Hz, 2H), 4.30 (s, 1H), 4.26 (s, 2H), 4.18 (s, 1H), 4.10 (s, 1H), 4.04-3.85 (m, 2H), 2.60-2.43 (m, 2H), 2.28 (s, 3H), 2.03 (td, J = 8.8, 4.1 Hz, 2H).
211	8.1	4- (aminomethyl) benzamide	4-((3-(2-(4-methylbenzoyl)-2- azaspiro[3.3]heptan-6- yl)ureido)methyl)benzamide. LCMS- ESI (POS.) m/z: 407 (M + H)+. 1H NMR (400 MHz, Methanol-d4) δ 7.72 (d, J = 8.3 Hz, 2H), 7.42 (t, J = 6.9 Hz, 2H), 7.26 (d, J = 8.4 Hz, 2H), 7.17 (d, J = 7.4 Hz, 2H), 4.30 (s, 1H), 4.25 (s, 2H), 4.18 (s, 1H), 4.10 (s, 1H), 4.02-3.86 (m, 2H), 2.50 (td, J = 9.7, 7.5, 3.4 Hz, 2H), 2.28 (s, 3H), 2.01 (td, J = 10.5, 3.4 Hz, 2H).
214	8.1	5- (aminomethyl) pyridin-2(1H)- one	1-(2-(4-methylbenzoyl)-2- azaspiro[3.3]heptan-6-yl)-3-((6-oxo-1,6- dihydropyridin-3-yl)methyl)urea. LCMS-ESI (POS.) m/z: 381 (M + H)+. 1H NMR (400 MHz, Methanol-d4) δ 7.50- 7.36 (m, 3H), 7.21 (s, 1H), 7.17 (d, J = 6.6 Hz, 2H), 6.42 (d, J = 9.3 Hz, 1H), 4.30 (s, 1H), 4.17 (s, 1H), 4.09 (s, 1H), 4.02- 3.85 (m, 4H), 2.48 (td, J = 8.0, 7.2, 3.5 Hz, 2H), 2.28 (s, 3H), 1.99 (ddd, J = 13.4, 8.1, 3.9 Hz, 2H).
215	8.1	5- (aminomethyl) picolinamide	5-((3-(2-(4-methylbenzoyl)-2- azaspiro[3.3]heptan-6- yl)ureido)methyl)picolinamide. LCMS- ESI (POS.) m/z: 408 (M + H)+. 1H NMR (400 MHz, Methanol-d4) δ 8.44 (d, J = 1.6 Hz, 1H), 7.95 (d, J = 8.0 Hz, 1H), 7.74 (dd, J = 8.0, 2.1 Hz, 1H), 7.43 (t, J = 6.8 Hz, 2H), 7.17 (d, J = 7.2 Hz, 2H), 4.31 (s, 1H), 4.29 (s, 2H), 4.18 (s, 1H), 4.10 (s, 1H), 4.03-3.84 (m, 2H), 2.59-2.42 (m, 2H), 2.29 (s, 3H), 2.02 (ddd, J = 12.7, 8.4, 3.4 Hz, 2H).
227	8.1	(1H-pyrazol- 4- yl)methanamine	1-((1H-pyrazol-4-yl)methyl)-3-(2-(4- methylbenzoyl)-2-azaspiro[3.3]heptan- 6-yl)urea. LCMS-ESI (POS.) m/z: 354 (M + H)+. 1H NMR (400 MHz, Methanol- d4) δ 8.04 (d, J = 4.2 Hz, 1H), 7.68-7.58 (m, 1H), 7.43 (t, J = 6.9 Hz, 2H), 7.17 (d, J = 6.3 Hz, 2H), 4.30 (s, 1H), 4.18 (s, 1H), 4.12 (d, J = 1.0 Hz, 2H), 4.10 (s, 1H), 3.98 (s, 1H), 3.91 (dt, J = 16.1, 8.1 Hz, 1H), 2.49 (ddt, J = 10.5, 7.5, 3.1 Hz, 2H), 2.29 (s, 3H), 2.00 (tt, J = 8.6, 2.9 Hz, 2H).
228	8.1	oxazol-4- ylmethanamine	1-(2-(4-methylbenzoyl)-2- azaspiro[3.3]heptan-6-yl)-3-(oxazol-4- ylmethyl)urea. LCMS-ESI (POS.) m/z: 355 (M + H)+. 1H NMR (400 MHz, Methanol-d4) δ 8.04 (d, J = 4.2 Hz, 1H), 7.70-7.59 (m, 1H), 7.43 (t, J = 6.9 Hz, 2H), 7.17 (d, J = 7.4 Hz, 2H), 4.30 (s, 1H), 4.18 (s, 1H), 4.12 (s, 2H), 4.10 (s, 1H), 3.98 (s, 1H), 3.91 (dt, J = 16.1, 8.1 Hz, 1H), 2.49 (ddt, J = 10.5, 7.5, 3.1 Hz, 2H), 2.29 (s, 3H), 2.00 (tt, J = 8.6, 2.9 Hz, 2H).
13	(4- aminopiperidin- 1- yl)(phenyl) methanone	4- (aminomethyl) benzamide	4-((3-(1-benzoylpiperidin-4- yl)ureido)methyl)benzamide. LCMS- ESI (POS.) m/z: 381 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.90 (s, 1H), 7.85- 7.77 (m, 2H), 7.45 (q, J = 2.8 Hz, 3H), 7.41-7.34 (m, 2H), 7.30 (d, J = 7.9 Hz, 3H), 6.35 (t, J = 6.1 Hz, 1H), 6.05 (d, J = 7.7 Hz, 1H), 4.25 (d, J = 6.0 Hz, 2H), 3.73- 3.60 (m, 1H), 3.51 (s, 1H), 3.05 (d, J = 41.0 Hz, 2H), 1.81 (d, J = 35.5 Hz, 2H), 1.42-1.19 (m, 3H).
282	17.1	(4- methoxyphenyl) methanamine	N-(2-fluorophenyl)-6-(3-(4- methoxybenzyl)ureido)-N- methylhexanamide. LCMS-ESI (POS.) m/z: 402.0 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 7.43 (dq, J = 30.9, 8.4 Hz, 3H), 7.30 (t, J = 7.6 Hz, 1H), 7.15 (d, J = 8.2 Hz, 2H), 6.86 (d, J = 8.2 Hz, 2H), 6.13 (s, 1H), 5.78 (q, J = 6.1 Hz, 1H), 4.10 (d, J = 5.9 Hz, 2H), 3.72 (s, 3H), 3.17 (d, J = 5.3 Hz, 1H), 3.11 (s, 2H), 2.91 (q, J = 6.5 Hz, 2H), 1.95 (dt, J = 24.5, 7.6 Hz, 2H), 1.43 (p, J = 7.1 Hz, 2H), 1.23 (q, J = 7.2 Hz, 2H), 1.11 (d, J = 7.8 Hz, 2H).
286	17.1	pyridin-4- ylmethanamine	N-(2-fluorophenyl)-N-methyl-6-(3- (pyridin-4-ylmethyl)ureido) hexanamide. LCMS-ESI (POS.) m/z: 373.2 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 8.52-8.40 (m, 2H), 8.14 (s, 1H), 7.44 (dq, J = 30.4, 9.0, 8.5 Hz, 2H), 7.30 (t, J = 7.6 Hz, 1H), 7.21 (t, J = 5.8 Hz, 2H), 6.38 (q, J = 6.0 Hz, 1H), 6.01 (dt, J = 18.7, 5.7 Hz, 1H), 4.21 (t, J = 6.0 Hz, 2H), 3.11 (s, 3H), 2.96 (dq, J = 27.7, 6.6 Hz, 2H), 2.07-1.83 (m, 2H), 1.42 (qd, J = 15.3, 14.7, 7.1 Hz, 2H), 1.26 (dd, J = 10.4, 7.0 Hz, 2H), 1.13 (d, J = 6.7 Hz, 2H).
287	17.1	(1H-pyrazol- 4- yl)methanamine	6-(3-((1H-pyrazol-4-yl)methyl)ureido)- N-(2-fluorophenyl)-N- methylhexanamide. LCMS-ESI (POS.) m/z: 362.0 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 12.57 (s, 1H), 7.44 (tt, J = 18.4, 8.3 Hz, 5H), 7.30 (t, J = 7.7 Hz, 1H), 5.90 (t, J = 5.6 Hz, 1H), 5.80-5.68 (m, 1H), 4.02 (d, J = 5.5 Hz, 2H), 3.11 (s, 3H), 2.90 (q, J = 6.6 Hz, 2H), 1.95 (dt, J = 23.9, 7.5 Hz, 2H), 1.43 (p, J = 7.4 Hz, 2H), 1.24 (dq, J = 14.4, 7.0 Hz, 2H), 1.16-1.03 (m, 2H).
288	17.1	oxazol-5- ylmethanamine	N-(2-fluorophenyl)-N-methyl-6-(3- (oxazol-5-ylmethyl)ureido) hexanamide. LCMS-ESI (POS.) m/z: 363.0 (M + H)+. 1H NMR (400 MHz, DMSO-d6) δ 8.25 (d, J = 3.3 Hz, 1H), 7.44 (dq, J = 30.7, 8.4 Hz, 2H), 7.30 (t, J = 7.4 Hz, 1H), 6.92 (d, J = 4.4 Hz, 1H), 6.25 (dt, J = 11.2, 5.7 Hz, 1H), 5.92 (dt, J = 18.9, 5.7 Hz, 1H), 4.24 (t, J = 5.7 Hz, 2H), 3.17 (d, J = 5.2 Hz, 2H), 3.11 (s, 2H), 2.94 (dq, J = 28.4, 6.6 Hz, 2H), 1.95 (dt, J = 24.3, 7.5 Hz, 2H), 1.41 (gd, J = 15.3, 14.4, 7.3 Hz, 2H), 1.25 (dd, J = 17.4, 8.9 Hz, 2H), 1.12 (t, J = 7.1 Hz, 2H).

Example 5

Preparation of N-(6-cyanopyridin-2-yl)-6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxamide (Compound 132)

N-(6-cyanopyridin-2-yl)-6-(3-(4-methoxybenzyl)ureido)-2-azaspiro[3.3]heptane-2-carboxamide. Phenyl (6-cyanopyridin-2-yl)carbamate (130 mg, 0.54 mmol, 1.5 equiv) was added to a stirring solution of 1-(4-methoxybenzyl)-3-(2-azaspiro[3.3]heptan-6-yl)urea (100 mg, 0.36 mmol, 1 equiv) in DMF (1 mL) at 25° C. After 12 h, the reactions were diluted with MeOH to a total volume of 1.8 mL, filtered through a 0.4 μm syringe filter, and product isolated by reverse phase HPLC (0->70% MeCN/H2O w/0.1% formic acid) as a white solid (39 mg, 26%). ¹H NMR (400 MHz, DMSO-d₆) δ 9.56 (s, 1H), 8.14 (dd, J=8.7, 1.8 Hz, 1H), 7.90-7.75 (m, 1H), 7.51 (dd, J=7.3, 1.8 Hz, 1H), 7.08 (d, J=7.9 Hz, 2H), 6.83-6.76 (m, 2H), 6.17-6.10 (m, 1H), 6.08 (d, J=8.1 Hz, 1H), 4.03 (d, J=5.8 Hz, 2H), 3.96 (s, 2H), 3.86 (d, J=10.2 Hz, 3H), 3.65 (s, 3H), 2.36 (t, J=8.8 Hz, 2H), 1.91 (t, J=9.5 Hz, 2H). LRMS (APCI) m/z 421.1 (M+H).

Compounds in the following table were prepared in a similar manner as Compound 132, using the intermediates and reagents as listed.

Compound
No.	Amine	Intermediate	Structure, Name and Data
133	phenyl (2- methyl- pyrimidin-5- yl)carbamate	3.2	6-(3-(4-methoxybenzyl)ureido)-N-(2- methylpyrimidin-5-yl)-2- azaspiro[3.3]heptane-2-carboxamide. LRMS (APCI) m/z 411 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.02 (s, 2H), 7.15 (d, J = 7.4 Hz, 2H), 6.87 (d, J = 7.0 Hz, 2H), 6.35-6.18 (m, 2H), 4.10 (d, J = 5.4 Hz, 2H), 4.01 (s, 2H), 3.95 (dd, J = 16.1, 8.2 Hz, 1H), 3.89 (s, 2H), 3.72 (s, 3H), 3.43-3.19 (m, 2H), 3.15 (s, 2H), 2.45 (t, J = 9.1 Hz, 2H), 2.00 (t, J = 9.4 Hz, 2H).

Example 6

Preparation of 1-(4-chlorobenzyl)-3-((2r,4s)-6-(2-methylpyridin-4-yl)-6-azaspiro[3.4]octan-2-yl)urea (Compound 171)

1-(4-chlorobenzyl)-3-((2r,4s)-6-(2-methylpyridin-4-yl)-6-azaspiro[3.4]octan-2-yl)urea. 1-(4-chlorobenzyl)-3-((2r,4s)-6-azaspiro[3.4]octan-2-yl)urea (Intermediate 3.5) (100 mg, 0.34 mmol, 1 equiv), 4-fluoro-2-methylpyridine (57 mg, 0.51 mmol, 1.5 equiv), and DIPEA (178 μL, 1.0 mmol, 3 equiv) were suspended in isopropanol (3 mL) before being heated to 150° C. in microwave for 30 min. The solvent was then removed by rotary evaporation and the desired product was isolated by reverse phase HPLC (05->95% MeCN/H2O w/0.1% formic acid) as a white solid (30 mg, 23%). LRMS (APCI) m/z 385 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.20 (s, 1H), 7.98 (d, J=6.1 Hz, 1H), 7.40-7.32 (m, 2H), 7.30-7.24 (m, 2H), 6.40-6.28 (m, 4H), 4.18 (d, J=6.0 Hz, 2H), 4.12 (q, J=8.1 Hz, 1H), 3.31 (t, J=6.7 Hz, 3H), 2.32 (s, 3H), 2.29-2.20 (m, 2H), 2.01 (t, J=6.7 Hz, 2H), 1.90 (td, J=8.8, 2.7 Hz, 2H).

Compounds in the following table were prepared in a similar manner as Compound 171, using the intermediates and reagents as listed.

Compound
No.	Amine	Intermediate	Structure, Name and Data
170	2- chloro- pyrimidine	3.5	1-(4-chlorobenzyl)-3-((2s,4r)-6-(pyrimidin-2- yl)-6-azaspiro[3.4]octan-2-yl)urea. LRMS (APCI) m/z 372 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.32 (d, J = 4.7 Hz, 2H), 7.41- 7.32 (m, 2H), 7.29-7.19 (m, 2H), 6.57 (t, J = 4.8 Hz, 1H), 6.33 (d, J = 7.6 Hz, 2H), 4.18 (d, J = 6.0 Hz, 2H), 4.09 (q, J = 8.1 Hz, 1H), 3.51 (s, 2H), 3.44 (t, J = 6.9 Hz, 2H), 2.31-2.21 (m, 2H), 1.96-1.81 (m, 4H).
183	2- fluoro- 6- methyl- pyridine	3.5	1-(4-chlorobenzyl)-3-((2r,4s)-6-(6- methylpyridin-2-yl)-6-azaspiro[3.4]octan-2- yl)urea. LRMS (APCI) m/z 385 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.41-7.30 (m, 3H), 7.26 (d, J = 8.4 Hz, 2H), 6.38 (d, J = 7.2 Hz, 1H), 6.34 (t, J = 6.0 Hz, 1H), 6.28 (d, J = 8.0 Hz, 1H), 6.17 (d, J = 8.4 Hz, 1H), 4.18 (d, J = 6.1 Hz, 2H), 4.11 (q, J = 8.2 Hz, 1H), 3.39- 3.24 (m, 5H), 2.27 (s, 3H), 2.22 (dd, J = 8.8, 2.9 Hz, 1H), 1.96 (t, J = 6.7 Hz, 2H), 1.89 (td, J = 8.7, 2.7 Hz, 2H).
199	2- fluoro- 6- methyl- pyridine	3.6	1-(4-chlorobenzyl)-3-((2s,4r)-6-(6- methylpyridin-2-yl)-6-azaspiro[3.4]octan-2- yl)urea. LRMS (APCI) m/z 385 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.14 (s, 1H), 7.41-7.34 (m, 2H), 7.26 (d, J = 8.4 Hz, 2H), 6.39 (d, J = 7.2 Hz, 1H), 6.32 (d, J = 8.2 Hz, 2H), 6.22 (d, J = 8.4 Hz, 1H), 4.18 (d, J = 6.0 Hz, 2H), 4.10 (p, J = 8.2 Hz, 1H), 3.41 (s, 4H), 2.31-2.18 (m, 5H), 1.98-1.77 (m, 4H).
307	2- fluoro- pyridine	3.8	1-(4-chlorobenzyl)-3-(4-(1-(pyridin-2- yl)piperidin-4-yl)butyl)urea. LRMS (APCI) m/z 401.2 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.08 (d, J = 4.9 Hz, 1H), 7.48 (t, J = 8.0 Hz, 1H), 7.37 (d, J = 8.1 Hz, 2H), 7.26 (d, J = 8.1 Hz, 2H), 6.79 (d, J = 8.7 Hz, 1H), 6.57 (dd, J = 7.0, 5.1 Hz, 1H), 6.31 (t, J = 6.2 Hz, 1H), 5.93 (d, J = 6.0 Hz, 1H), 4.27 (d, J = 13.0 Hz, 2H), 4.18 (d, J = 5.9 Hz, 2H), 3.00 (q, J = 6.5 Hz, 2H), 2.73 (t, J = 12.5 Hz, 2H), 1.69 (d, J = 12.9 Hz, 2H), 1.45 (s, 1H), 1.37 (t, J =7.0Hz, 2H), 1.32-1.24 (m, 2H), 1.23 (d, J = 7.0 Hz, 2H), 1.09 (dd, J = 18.1, 8.1 Hz, 2H).
308	4- fluoro- pyridine	3.8	1-(4-chlorobenzyl)-3-(4-(1-(pyridin-4- yl)piperidin-4-yl)butyl)urea. LRMS (APCI) m/z 401.2 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.15 (s, 1H), 7.37 (d, J = 8.1 Hz, 2H), 7.26 (d, J = 8.1 Hz, 2H), 6.99 (s, 1H), 6.35 (t, J = 6.1 Hz, 1H), 5.97 (t, J = 5.7 Hz, 1H), 4.17 (d, J = 6.1 Hz, 2H), 4.05 (d, J = 13.2 Hz, 2H), 3.17 (s, 2H), 3.02 (d, J = 6.4 Hz, 1H), 3.00- 2.90 (m, 3H), 1.75 (dd, J = 13.2, 3.2 Hz, 2H), 1.54 (s, 1H), 1.36 (q, J = 6.6, 6.2 Hz, 2H), 1.25 (dq, J = 21.0, 7.7, 6.6 Hz, 4H), 1.09 (qd, J = 12.4, 3.9 Hz, 2H).

Example 7

Preparation of 1-(6-((5,7-difluoro-3,4-dihydroquinolin-1(2H)-yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea (Compound 127)

1-(6-((5,7-difluoro-3,4-dihydroquinolin-1(2H)-yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea. (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl methanesulfonate (Intermediate 4.1) (60 mg, 0.16 mmol, 1.0 equiv) and 5,7-difluoro-1,2,3,4-tetrahydroquinoline (21 mg, 0.19 mmol) were dissolved in DMF (0.5 mL) and potassium carbonate (1.5 equiv) was added. The reaction was stirred at 80° C. for 12 hours. Potassium carbonate was filtered off and the solution was directly purified by reverse phase HPLC with a 10%-100% acetonitrile in water solution that was run over 30 minutes in a Phenomonex Gemini 5u C18 column, providing the desired product (18.0 mg, 24% yield) as a white foam. LCMS-APCI (POS.) m/z: 456.2 (M+H)⁺. ¹H NMR (400 MHz, DMSO-d₆) δ 7.17 (dd, J=12.2, 2.9 Hz, 2H), 6.99 (d, J=13.8 Hz, 2H), 6.86 (dd, J=8.5, 2.9 Hz, 2H), 6.08 (d, J=11.9 Hz, 2H), 4.09 (d, J=4.6 Hz, 2H), 4.03-3.76 (m, 1H), 3.72 (d, J=3.0 Hz, 3H), 3.60 (d, J=7.0 Hz, 2H), 2.85 (dd, J=7.4, 2.4 Hz, 2H), 2.70 (d, J=8.4 Hz, 2H), 2.34 (s, 2H), 2.27-1.91 (m, 5H), 1.90-1.56 (m, 4H).

Compounds in the following table were prepared in a similar manner as Compound 127, using the intermediates and reagents as listed.

Compound
No.	Amine	Intermediate	Structure, Name and Data
128	indoline	4.1	1-(6-(indolin-1-ylmethyl)spiro[3.3]heptan- 2-yl)-3-(4-methoxybenzyl)urea. LRMS (APCI) m/z 406 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.72 (dd, J = 11.2, 3.4 Hz, 2H), 7.55 (dd, J = 11.2, 5.5 Hz, 1H), 7.17 (dd, J = 11.2, 5.5 Hz, 2H), 7.01 (d, J = 13.8 Hz, 2H), 6.84 (dd, J = 8.5, 2.9 Hz, 2H), 6.14 (d, J = 11.9 Hz, 1H), 4.14 (d, J = 4.6 Hz, 2H), 4.05 (s, 1H), 3.76 (d, J = 3.0 Hz, 3H), 3.55 (d, J = 7.0 Hz, 2H), 3.32-3.29 (m, 3H), 2.85 (dd, J = 7.2, 2.6 Hz, 2H), 2.31 (s, 2H), 2.34-1.99 (m, 3H), 1.89-1.51 (m, 3H).
129	isoindoline	4.1	1-(6-(isoindolin-2- ylmethyl)spiro[3.3]heptan-2-yl)-3-(4- methoxybenzyl)urea. LRMS (APCI) m/z 406 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.24 (dd, J = 15.2, 2.9 Hz, 2H), 7.17 (dd, J = 12.2, 2.9 Hz, 2H), 6.99 (d, J = 13.8 Hz, 2H), 6.83 (dd, J = 8.5, 2.9 Hz, 2H), 6.14 (d, J = 11.9 Hz, 2H), 4.09 (d, J = 4.6 Hz, 2H), 4.08- 3.89 (m, 1H), 3.74 (d, J = 3.0 Hz, 3H), 3.66 (d, J = 6.8 Hz, 1H), 2.86 (dd, J = 7.4, 2.4 Hz, 4H), 2.79 (d, J = 8.4 Hz, 2H), 2.32 (s, 2H), 2.32-1.99 (m, 3H), 1.91-1.50 (m, 3H).
134	1H- indazol	4.1	1-(6-((1H-indazol-1- yl)methyl)spiro[3.3]heptan-2-yl)-3-(4- methoxybenzylurea. LRMS (APCI) m/z 405 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.51 (d, J = 4.6 Hz, 1H), 7.78 (td, J = 7.7, 1.8 Hz, 1H), 7.45 (d, J = 7.7 Hz, 1H), 7.28 (dd, J = 7.4, 5.0 Hz, 1H), 7.14 (d, J = 8.5 Hz, 3H), 6.86 (d, J = 8.5 Hz, 2H), 6.16-5.92 (m, 2H), 4.09 (d, J = 5.9 Hz, 2H), 3.98-3.84 (m, 1H), 3.72 (s, 3H), 3.67 (s, 1H), 3.46 (d, J = 5.3 Hz, 2H), 3.18 (p, J = 8.6 Hz, 1H), 2.48- 2.30 (m, 2H), 2.24-2.06 (m, 2H), 2.01 (ddd, J = 11.5, 8.5, 2.8 Hz, 1H), 1.79 (dd, J = 10.7, 8.6 Hz, 1H), 1.69 (dd, J = 11.0, 8.7 Hz, 1H).
52	2- phenyl- pyrrolidine	4.1	1-(4-methoxybenzyl)-3-(6-((2- phenylpyrrolidin-1- yl)methyl)spiro[3.3]heptan-2-yl)urea. LRMS (APCI) m/z 434 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 7.31 (t, J = 4.0 Hz, 4H), 7.23 (q, J = 4.4 Hz, 1H), 7.13 (d, J = 8.3 Hz, 2H), 6.86 (d, J = 8.4 Hz, 2H), 6.16-5.90 (m, 2H), 4.07 (d, J = 5.9 Hz, 2H), 3.85 (q, J = 8.0 Hz, 1H), 3.72 (s, 4H), 3.17 (td, J = 8.4, 2.6 Hz, 2H), 2.37 (ddd, J = 12.5, 8.5, 4.5 Hz, 1H), 2.25 (dq, J = 14.7, 7.3 Hz, 2H), 2.15-1.98 (m, 3H), 1.90 (dtt, J = 12.5, 7.8, 3.8 Hz, 1H), 1.84-1.63 (m, 3H), 1.62-1.33 (m, 5H).

Example 8

Preparation of 1-(4-chlorobenzyl)-3-((2r,4s)-6-(2-methylpyridin-4-yl)-6-azaspiro[3.4]octan-2-yl)urea (Compound 16)

Step 1: Phenyl (4-(1-benzoylpiperidin-4-yl)butyl)carbamate. NEt₃ (583 mg, 5.76 mmol, 3 equiv) and phenyl chloroformate (360.79 mg, 2.304 mmol, 1.2 equiv) were added to a stirring solution of 4-(1-benzoylpiperidin-4-yl)butan-1-amine (prepared as previously described in “Gillig, A., Majjigapu, S. R., Sordat, B. and Vogel, P. (2012), Synthesis of a C-Iminoribofuranoside Analog of the Nicotinamide Phosphoribosyltransferase (NAMPT) Inhibitor FK866. HCA, 95: 34-42”) (500 mg, 1.92 mmol, 1.00 equiv) in CH₂Cl₂ (5 mL) at 0° C. before being warmed to rt. After 4 h, the reaction was concentrated by rotary evaporation and the product isolated by prep-TLC (PE/EtOAc 1:1) as a yellow oil (41%). LRMS (ESI) m/z 381 (M+H).

Step 2: 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea. NEt₃ ((119 mg, 1.2 mmol, 3.00 equiv) was added to a stirring solution of phenyl N-[4-(1-benzoylpiperidin-4-yl)butyl]carbamate (150 mg, 0.4 mmol, 1.00 equiv) and 1-(4-chlorophenyl)methanamine (167 mg, 1.18 mmol, 3.00 equiv) in CH₂Cl₂ (2 mL) at rt. After 12 h, the solvent was removed by rotary evaporation and the product isolated by reverse phase HPLC (30%->60% MeCN/H2O w/0.1% ammonium formate) as a white solid (31%). LRMS (ESI) m/z 428 (M+H). ¹H NMR (300 MHz, DMSO-d₆) δ 7.48 (m, 3H), 7.31 (m, 4H), 7.21 (m, 2H), 6.30 (t, J=6.1 Hz, 1H), 5.92 (t, J=5.7 Hz, 1H), 4.46 (s, 1H), 4.17 (d, J=6.0 Hz, 2H), 3.55 (s, 1H), 3.00 (q, J=6.4 Hz, 3H), 2.81 (m, 1H), 1.70 (s, 2H), 1.48 (s, 1H), 1.36 (s, 2H), 1.24 (s, 4H), 1.06 (s, 2H).

Compounds in the following table were prepared in a similar manner as Compound 16, using the intermediates and reagents as listed.

Compound
No.	Amine	Intermediate	Structure, Name and Data
22	[4- (amino methyl) phenyl] methanol	4-(1- benzoylpiperidin- 4-yl)butan- 1-amine	1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4- (hydroxymethyl)benzyl)urea. LRMS (ESI) m/z 424 (M + H). 1H NMR (400 MHz, Methanol-d4) δ 7.31-7.22 (m, 3H), 7.24- 7.16 (m, 2H), 7.09 (q, J = 8.2 Hz, 4H), 4.61 (d, J = 12.3 Hz, 3H), 4.38 (s, 2H), 3.67 (d, J = 13.4 Hz, 1H), 3.14 (m, 2H), 3.06 (m, 1H), 2.96 (t, J = 6.8 Hz, 1H), 1.87 (s, 1H), 1.65 (s, 2H), 1.49 (d, J = 13.0 Hz, 2H), 1.36 (m, 4H), 1.36 (m, 2H).
1	pyridin- 4- ylmethan- amine	4-(1- benzoylpiperidin- 4-yl)butan- 1-amine	1-(4-(1-benzoylpiperidin-4-yl)butyl)-3- (pyridin-4-ylmethyl)urea. LRMS (ESI) m/z 395 (M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.47 (d, J = 4.6 Hz, 2H), 7.50-7.40 (m, 3H), 7.36 (dd, J = 6.7, 3.0 Hz, 2H), 7.22 (d, J = 5.0 Hz, 2H), 6.40 (t, J = 6.1 Hz, 1H), 6.03 (t, J = 5.8 Hz, 1H), 4.45 (s br, 1H), 4.22 (d, J = 5.8 Hz, 2H), 3.55 (s br, 1H), 3.01 (q, J = 6.1 Hz, 3H), 2.74 (s br, 1H), 1.73 (s br, 1H), 1.60 (s br, 1H), 1.49 (s br, 1H), 1.37 (d, J = 7.0 Hz, 2H), 1.25 (s, 4H), 1.06 (s br, 2H).
17	(1H- pyrazol- 4- yl)methan- amine	5.1	N-(6-(3-((1H-pyrazol-4- yl)methyl)ureido)spiro[3.3]heptan-2- yl)benzamide. LRMS (ESI) m/z 354 (M + H). 1H NMR (300 MHz, DMSO-d6) δ 12.52 (s, 1H), 8.46 (d, J = 7.5 Hz, 1H), 7.75 (d, J = 7.2 Hz, 2H), 7.44 (t, J = 7.2 Hz, 1H), 7.37 (t, J = 7.4 Hz, 3H), 5.96 (d, J = 8.1 Hz, 1H), 5.83 (t, J = 5.6 Hz, 1H), 4.23 (h, J = 8.4 Hz, 1H), 3.95 (d, J = 5.5 Hz, 2H), 3.88 (dt, J = 16.2, 8.2 Hz, 1H), 2.5 (m, 1H), 2.30 (ddd, J = 12.0, 7.6, 5.1 Hz, 2H), 2.13 (dt, J = 12.3, 6.1 Hz, 2H), 2.01 (dt, J = 19.7, 10.2 Hz, 2H), 1.73 (dt, J = 19.4, 9.9 Hz, 2H).
14	4- (amino methyl) benzamide	5.1	N-(6-(3-(4- carbamoylbenzyl)ureido)spiro[3.3]heptan- 2-yl)benzamide. LRMS (ESI) m/z 407 (M + H). 1H NMR (300 MHz, DMSO-d6) δ 8.54 (d, J = 7.3 Hz, 1H), 7.90 (s, 1H), 7.82 (t, J = 6.7 Hz, 4H), 7.51 (t, J = 7.0 Hz, 1H), 7.45 (t, J = 7.4 Hz, 2H), 7.29 (d, J = 7.8 Hz, 3H), 6.29 (t, J = 5.9 Hz, 1H), 6.21 (d, J = 7.9 Hz, 1H), 4.31 (h, J = 8.2 Hz, 1H), 4.23 (d, J = 5.8 Hz, 2H), 3.98 (h, J = 8.5 Hz, 1H), 2.38 (p, J = 5.4 Hz, 2H), 2.21 (q, J = 6.4 Hz, 2H), 2.09 (dt, J = 19.6, 10.2 Hz, 2H), 1.85 (dt, J = 18.9, 9.6 Hz, 2H).
15	pyridin- 4- ylmethan- amine	5.1	N-(6-(3-(pyridin-4- ylmethyl)ureido)spiro[3.3]heptan-2- yl)benzamide. LRMS (ESI) m/z 365 (M + H). 1H NMR (300 MHz, DMSO-d6) δ 8.57-8.43 (m, 3H), 7.87-7.77 (m, 2H), 7.56-7.45 (m, 1H), 7.44 (dd, J = 8.1, 6.2 Hz, 2H), 7.25- 7.17 (m, 2H), 6.40-6.25 (m, 2H), 4.30 (q, J = 8.0 Hz, 1H), 4.20 (d, J = 5.9 Hz, 2H), 3.96 (q, J = 8.0 Hz, 1H), 2.37 (ddd, J = 10.6, 7.5, 5.0 Hz, 2H), 2.14 (dtd, J = 31.5, 11.5, 7.7 Hz, 4H), 1.94-1.77 (m, 2H).
18	(4- phenyl) methan- amine methoxy	5.1	N-(6-(3-(4- methoxybenzyl)ureido)spiro[3.3]heptan-2- yl)benzamide. LRMS (ESI) m/z 394 (M + H). 1H NMR (300 MHz, DMSO-d6) δ 8.54 (d, J = 7.5 Hz, 1H), 7.83 (d, J = 7.5 Hz, 2H), 7.51 (t, J = 7.2 Hz, 1H), 7.45 (t, J = 7.4 Hz, 2H), 7.16 (d, J = 8.2 Hz, 2H), 6.87 (d, J = 8.2 Hz, 2H), 6.11 (d, J = 8.6 Hz, 2H), 4.30 (h, J = 8.4 Hz, 1H), 4.10 (d, J = 5.7 Hz, 2H), 3.97 (q, J = 7.5 Hz, 1H), 3.73 (s, 3H), 2.37 (q, J = 6.2 Hz, 2H), 2.19 (p, J = 5.6 Hz, 2H), 2.09 (dt, J = 19.4, 10.0 Hz, 2H), 1.82 (dt, J = 18.8, 9.9 Hz, 2H).

Example 9

Preparation of 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-methoxybenzyl)urea (Compound 20)

Step 1: Phenyl (4-carbamoylbenzyl)carbamate. NEt₃ (1.6 g, 16.1 mmol, 3.0 equiv) and phenyl chloroformate (1.0 g, 5.9 mmol, 1.10 equiv) were added to a stirring solution of 4-(aminomethyl)benzamide hydrochloride (1.0 g, 5.4 mmol, 1.0 equiv) in CH₂Cl₂ (10 mL) at 0° C. After 2 h, the reaction was quenched with water (20 mL), extracted with CH₂Cl₂ (2×20 mL), organics combined, washed with saturated sodium chloride (20 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product (1.2 g) as a white solid which was used in the future steps without further purification. LRMS (ESI) m/z 271 (M+H).

Step 2: 1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(4-methoxybenzyl)urea. NEt₃ (291 mg, 2.9 mmol, 5 equiv) was added to a stirring solution of 4-(1-benzoylpiperidin-4-yl)butan-1-amine (150 mg, 0.6 mmol, 1.00 equiv) and phenyl N-[(4-methoxyphenyl)methyl]carbamate (518 mg, 2.0 mmol, 3.5 equiv) in DMF (3 mL) at rt. After 12 h, the reaction was quenched with water (20 mL), extracted with EtOAc (2×20 mL). Organics were combined, washed with saturated sodium chloride (20 mL), dried over sodium sulfate, filtered, and solvent removed by rotary evaporation. The product was then isolated by reverse phase HPLC (30%->60% MeCN/H2O w/0.1% ammonium formate) as yellow tinged solid (82 mg). LRMS (ESI) m/z 424 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.49 (m, 3H), 7.42 (m, 2H), 7.23 (m, 2H), 6.88 (m, 2H), 4.60 (d, J=13.1 Hz, 1H), 4.22 (s, 2H), 3.75 (s, 3H), 3.69 (d, J=13.3 Hz, 1H), 3.13 (t, J=6.8 Hz, 3H), 2.84 (d, J=13.1 Hz, 1H), 1.83.

Compounds in the following table were prepared in a similar manner as Compound 20, using the intermediates and reagents as listed.

Compound	Amine -	Amine -
No.	step 1	step 2	Structure, Name and Data
19	4- (aminometh- yl)benz- amide	4-(1- benzoyl- piperidin-4- yl)butan- 1-amine
			4-((3-(4-(1-benzoylpiperidin-4-
			yl)butyl)ureido) methyl)benzamide. LRMS
			(ESI) m/z 437 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.85 (m, 2H), 7.45 (dd, J = 5.0,
			2.0 Hz, 3H), 7.41 - 7.33 (m, 4H), 4.60 (d, J =
			11.7 Hz, 1H), 4.36 (s, 2H), 3.69 (d, J = 13.5 Hz,
			1H), 3.14 (t, J = 6.9 Hz, 2H), 3.05 (d, J = 14.2
			Hz, 1H), 2.83 (s, 1H), 1.82 (s, 2H), 1.67 (s, 3H),
			1.47 (q, J = 7.2 Hz, 4H), 1.33 (t, J = 5.7 Hz,
			2H).
23	oxazol-5- ylmethan- amine	4-(1- benzoyl- piperidin-4- yl)butan- 1-amine
			1-(4-(1-benzoylpiperidin-4-yl)butyl)-3-
			(oxazol-5-ylmethyl)urea. LRMS (ESI) m/z 385
			(M + H). 1H NMR (300 MHz, DMSO-d6) δ 8.24
			(s, 1H), 7.46 - 7.38 (m, 3H), 7.37 - 7.34 (m,
			2H), 6.92 (S, 1H), 6.26 (t, J = 5.7 Hz, 1H), 5.94
			(t, J = 5.4 Hz, 1H), 4.45 (s, 1H), 4.26 (m, 2H),
			3.54 (s, 1H), 2.98 (t, J = 6 Hz, 3H), 2.76 (s, 1H),
			1.70 - 1.66 (m, 3H), 1.55 - 1.31 (m, 6H), 1.24-
			1.03 (m, 2H).
26	4- (aminometh- yl)benz- amide	6.1
			4-((3-(6-(pyridin-2-ylamino)spiro[3.3]heptan-
			2-yl)ureido)methyl)benzamide. LRMS (ESI)
			m/z 380 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.97 - 7.86
			(m, 2H), 7.81 (d, J = 8.1 Hz, 2H), 7.33 (t, J =
			7.7 Hz, 1H), 7.28 (d, J = 8.0 Hz, 3H), 6.62 (d, J =
			7.2 Hz, 1H), 6.49 - 6.40 (m, 1H), 6.36 (d, J =
			8.4 Hz, 1H), 6.28 (t, J = 5.7 Hz, 1H), 6.21 (d, J =
			8.0 Hz, 1H), 4.22 (d, J = 6.0 Hz, 2H), 4.13 (h,
			J = 7.9 Hz, 1H), 3.97 (h, J = 8.1 Hz, 1H), 2.41
			(ddt, J = 24.5, 12.1, 5.7 Hz, 2H), 2.31 - 2.11
			(m, 2H), 1.95 - 1.72 (m, 4H).
21	4- (amino- methyl)benz- amide	7.1
			4-((3-((1r,3r)-3-
			(benzylcarbamoyl)cyclobutyl)ureido)
			methyl)benzamide. LRMS (ESI) m/z 381
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ 8.25
			(t, J = 6.0 Hz, 1H), 7.90 (s, 1H), 7.81 (d, J = 7.9
			Hz, 2H), 7.30 (t, J = 8.0 Hz, 5H), 7.24 (d, J =
			7.1 Hz, 3H), 6.41 - 6.23 (m, 2H), 4.25 (dd, J =
			18.9, 6.1 Hz, 5H), 2.95 - 2.78 (m, 1H), 2.36 (t,
			J = 8.7 Hz, 2H), 2.04 (dt, J = 11.8, 9.3 Hz, 2H).

Example 10

Preparation of 1-(4-methoxybenzyl)-3-(5-phenoxypentyl)urea (Compound 149)

Step 1: 1-(5-hydroxypentyl)-3-(4-methoxybenzyl)urea. Phenyl N-[(4-methoxyphenyl) methyl]carbamate (250 mg, 1.0 mmol, 1.00 equiv), 5-aminopentanol (120 mg, 1.2 mmol, 1.2 equiv), and NEt₃ (295 mg, 2.9 mmol, 3 equiv) were dissolved in THF (5 mL) and heated to 65° C. After 1 h, the reaction was cooled to rt, quenched with H₂O (20 mL), extracted with EtOAc (2×20 mL), organics combined and washed with sat sodium chloride (20 mL). The organic layer was then dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product as a white solid (250 mg). LRMS (ESI) m/z 267 (M+H).

Step 2: 5-(3-(4-methoxybenzyl)ureido)pentyl methanesulfonate. MsCl (226 mg, 1.9 mmol, 2.50 equiv) was added to a stirring solution of 3-(5-hydroxypentyl)-1-[(4-methoxyphenyl)methyl]urea (210 mg, 0.79 mmol, 1.00 equiv) and NEt₃ (399 mg, 3.9 mmol, 5 equiv) in CH₂Cl₂ (5 mL) at 0° C. before being warmed to rt. After 1 h, the reaction was quenched with H₂O (20 mL), extracted with EtOAc (2×20 mL), organics combined and washed with sat sodium chloride (20 mL). The organic layer was then dried over sodium sulfate, filtered, and solvent removed by rotary evaporation to give the crude product as a white solid (440 mg). LRMS (ESI) m/z 345 (M+H).

Step 3: 1-(4-methoxybenzyl)-3-(5-phenoxypentyl)urea. 5-([[(4-Methoxyphenyl)methyl] carbamoyl]amino)pentyl methanesulfonate (350 mg, 1.0 mmol, 1.00 equiv), K₂CO₃ (351 mg, 2.5 mmol, 2.5 equiv), phenol (115 mg, 1.2 mmol, 1.2 equiv) and KI (16.9 mg, 0.10 mmol, 0.1 equiv) were suspended in DMSO (5 mL) before being heated to 80° C. After 2 h, the reaction was cooled to rt and product isolated by reverse phase HPLC (50% MeCN/H2O w/0.5% ammonium formate) as a white solid (15 mg). LRMS (ESI) m/z 343 (M+H). ¹H NMR (300 MHz, DMSO-d₆) δ 7.32-7.21 (m, 2H), 7.15 (d, J=8.6 Hz, 2H), 6.95-6.81 (m, 5H), 6.16 (t, J=6.2 Hz, 1H), 5.86 (s, 1H), 4.11 (d, J=5.8 Hz, 2H), 3.93 (t, J=6.4 Hz, 2H), 3.71 (s, 3H), 3.02 (d, J=6.0 Hz, 2H), 1.70 (t, J=6.8 Hz, 2H), 1.41 (s, 4H).

Compounds in the following table were prepared in a similar manner as Compound 149, using the intermediates and reagents as listed.

Compound
No.	Amine	Carbamate	Structure, Name and Data
150	6- amino- hexanol	Phenyl N- [(4- methoxyphe- nyl) methyl]carba- mate
			1-(4-methoxybenzyl)-3-(6-
			phenoxyhexyl)urea. LRMS (ESI) m/z 357
			(M + H). 1H NMR (300 MHz, DMSO-d6) δ 7.26
			(dd, J 8.5, 7.3 Hz, 2H), 7.15 (d, J = 8.6 Hz,
			2H), 6.95 - 6.81 (m, 5H), 6.14 (t, J = 5.9 Hz,
			1H), 5.84 (t, J = 5.7 Hz, 1H), 4.11 (d, J = 5.9
			Hz, 2H), 3.94 (t, J = 6.5 Hz, 2H), 3.71 (s, 3H),
			3.04 - 2.93 (m, 2H), 1.68 (q, J = 7.0 Hz, 2H),
			1.38 (s, 5H), 1.44 - 1.32 (m, 1H). ).
196	2-(2- amino- ethoxy) ethan-1- ol	Phenyl N- [(4- chlorophenyl) methyl]carba- mate
			1-(4-chlorobenzyl)-3-(2-(2-
			phenoxyethoxy)ethyl)urea. LRMS (APCI)
			m/z 349 (M + H). 1H NMR (400 MHz,
			Methanol-d4) δ 7.16 (td, J = 8.2, 5.4 Hz, 6H),
			6.87 - 6.76 (m, 3H), 4.17 (s, 2H), 4.05 - 3.94
			(m, 2H), 3.76 - 3.67 (m, 2H), 3.50 (t, J = 5.4
			Hz, 2H), 3.24 (t, J = 5.4 Hz, 2H).

Example 11

Preparation of N-benzyl-2-(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)-N-methylacetamide Compound 67)

Step 1: Preparation of (6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl cyanide.

(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl methanesulfonate (Intermediate 4.1) (0.1 g, 0.27 mmol, 1.0 equiv) was dissolved in DMF (1 mL) and sodium cyanide (5 eq) was added. The solution was stirred at 80° C. overnight and monitored by LCMS analysis. The solution was cooled to 0° C. and saturated aq. ammonium chloride solution (8 mL) and EtOAc (5 mL) was added and the solution stirred vigorously for 10 mins. The organic layer was separated, and the aq. layer was extracted with 10 mL of EtOAc. The combined organic layers were washed with brine, dried, filtered, and concentrated to provide the product as a white solid 72 mg, 87% yield). LCMS-APCI (POS.) m/z: 314.0 (M+H)+.

Step 2: N-benzyl-2-(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)-N-methylacetamide.

(6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl cyanide (50 mg, 0.17 mmol, 1.0 equiv) and N-methyl benzylamine (19 mg, 0.17 mmol, 1.0 equiv) were dissolved in toluene (0.5 mL) and methanesulfonic acid (16 mg, 0.17 mmol, 1.0 equiv) was added. The reaction was stirred at 110° C. for 24 hours. The solution was cooled to rt and quenched with saturated aq. sodium bicarbonate. The reaction was extracted with DCM and the combined organic layers were dried, filtered and concentrated. The organic phase was dried to a viscous oil which was purified by reverse phase HPLC with a 10%-100% acetonitrile in water solution that was run over 30 minutes in a Phenomonex Gemini 5u C₁₈ column, providing the desired product (51.0 mg, 0.12 mmol, 69% yield) as a white solid. LCMS-APCI (POS.) m/z: 436.0 (M+H)+. 1H NMR (400 MHz, DMSO-d₆) δ 7.33 (tt, J=24.0, 7.5 Hz, 3H), 7.16 (dd, J=13.3, 7.3 Hz, 4H), 6.86 (d, J=8.0 Hz, 2H), 6.22-5.97 (m, 2H), 4.55 (s, 1H), 4.47 (s, 1H), 4.09 (t, J=4.3 Hz, 2H), 3.90 (dq, J=15.0, 8.0 Hz, 1H), 3.72 (d, J=1.6 Hz, 3H), 2.88 (s, 2H), 2.78 (s, 2H), 2.45 (d, J=16.9 Hz, 3H), 2.34 (q, J=9.3, 7.5 Hz, 1H), 2.16 (s, 1H), 2.04 (dd, J=15.8, 9.5 Hz, 1H), 1.68 (dh, J=37.2, 9.6 Hz, 4H).

Example 12

Preparation of 1-(4-chlorobenzyl)-3-(6-(dibenzylamino)spiro[3.3]heptan-2-yl)urea (Compound 119)

Step 1: Preparation of 1-(4-chlorobenzyl)-3-(6-(dibenzylamino)spiro[3.3]heptan-2-yl)urea.

Benzyl bromide (18 μL, 0.159 mmol, 1 equiv) was added to a stirring solution of 1-(6-aminospiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (70 mg, 0.238 mmol, 1.5 equiv) and DIPEA (83 μL, 0.477 mmol, 3 equiv) in CH₂Cl₂ (2 mL) at rt. After 3 h, solvent was removed by rotary evaporation and product isolated by reverse phase HPLC (5->95% MeCN/H2O w/0.1% formic acid) as a white solid (28 mg, 40%). LRMS (APCI) m/z 474 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.14 (s, 1H), 7.41-7.15 (m, 14H), 6.25 (t, J=6.1 Hz, 1H), 6.15 (d, J=8.1 Hz, 1H), 4.14 (d, J=6.0 Hz, 2H), 3.90 (q, J=8.0 Hz, 1H), 3.40 (s, 3H), 3.18 (d, J=3.9 Hz, 1H), 2.99 (q, J=7.9 Hz, 1H), 2.24 (dt, J=11.3, 5.8 Hz, 1H), 2.09 (dq, J=10.0, 5.2, 4.5 Hz, 2H), 1.89 (dt, J=11.5, 5.8 Hz, 1H), 1.75 (qd, J=13.0, 11.8, 9.0 Hz, 3H).

Example 13

Preparation of 4-(4-(6-(benzylamino)spiro[3.3]heptan-2-yl)-3-oxobutyl)benzamide (Compound 24)

Step 1: Preparation of tert-butyl (6-(4-(4-carbamoylphenyl)-2-oxobutyl)spiro[3.3]heptan-2-yl)carbamate. Phenyl N-[(4-carbamoylphenyl)methyl]carbamate (657 mg, 2.4 mmol, 1.1 equiv) and NEt₃ (671 mg, 6.6 mmol, 3.00 equiv) were added to a stirring solution of N-[6-aminospiro[3.3]heptan-2-yl]carbamate (500 mg, 2.2 mmol, 1.00 equiv) in DMF (5.00 mL) before being heated to 50° C. After 2 h, the reaction was cooled to rt, and volatiles were removed by rotary evaporation. The product was isolated by reverse phase HPLC (60% MeCN/H2O w/0.1% ammonium formate) as a white solid (45%). LRMS (ESI) m/z 403 (M+H).

Step 2: Preparation of 4-(4-(6-aminospiro[3.3]heptan-2-yl)-3-oxobutyl)benzamide hydrochloride. HCl (10 mL, 4M in dioxanes) was added to a stirring solution of tert-butyl (6-(4-(4-carbamoylphenyl)-2-oxobutyl)spiro[3.3]heptan-2-yl)carbamate carbamate (380 mg, 0.94 mmol, 1.00 equiv) in CH₂Cl₂ (40 mL) at rt. After 1 h, the reaction was concentrated by rotary evaporation to afford the crude product (560 mg) as a white solid which was used without further purification. LRMS (ESI) m/z 303 (M+H).

Step 3: Preparation of 4-(4-(6-(benzylamino)spiro[3.3]heptan-2-yl)-3-oxobutyl)benzamide

AcOH (29 mg, 0.54 mmol, 2 equiv) and NaHB(OAc)₃ (103 mg, 0.54 mmol, 2.00 equiv) were added to a stirring solution of 4-[[([6-aminospiro[3.3]heptan-2-yl]carbamoyl)amino] methyl]benzamide hydrochloride (82 mg, 0.27 mmol, 1.00 equiv) and benzaldehyde (29 mg, 0.27 mmol, 1.00 equiv) in CH₂Cl₂ (5 mL) at rt. After 3 h, the solvent was removed by rotary evaporation and product isolated by reverse phase HPLC (15%->45% MeCN/H2O w/0.1% ammonium formate) as a white solid (15%). LRMS (ESI) m/z 393 (M+H). ¹H NMR (300 MHz, Methanol-d₄) δ 7.90 (s, 1H), 7.80 (d, J=7.8 Hz, 2H), 7.28 (s, 6H), 7.23-7.09 (m, 1H), 6.26 (s, 1H), 6.16 (d, J=8.1 Hz, 1H), 4.21 (d, J=4.6 Hz, 2H), 3.92 (d, J=7.9 Hz, 1H), 3.57 (s, 2H), 3.32 (s, 3H), 3.11-2.92 (m, 1H), 2.23 (s, 2H), 2.12 (s, 1H), 2.03 (d, J=7.6 Hz, 1H), 1.73 (dt, J=20.4, 10.2 Hz, 3H).

Example 14

Preparation of 4-((3-(6-((pyridin-2-ylmethyl)amino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide (Compound 34)

Step 1: Preparation of 6-aminospiro[3.3]heptan-2-one hydrochloride. HCl (5 mL, 4M in dioxanes) was added to a stirring solution of tert-butyl N-[6-oxospiro[3.3]heptan-2-yl]carbamate (500 mg, 2.2 mmol, 1.00 equiv) in CH₂Cl₂ (5.00 mL). The reaction was then concentrated by rotary evaporation to give the crude product (350 mg) as a white solid. LRMS (ESI) m/z 126 (M+H).

Step 2: Preparation of 4-((3-(6-oxospiro[3.3]heptan-2-yl)ureido)methyl)benzamide. N-[(4-carbamoylphenyl) methyl]carbamate (241 mg, 0.90 mmol, 1.2 equiv) and NEt₃ (300 mg, 2.97 mmol, 4 equiv) were added to a stirring solution of 6-aminospiro[3.3]heptan-2-one hydrochloride (120 mg, 0.74 mmol, 1.00 equiv) in MeCN (4 mL) and heated to 65° C. After 2 h, the reaction was cooled to rt and concentrated by rotary evaporation to give the crude product (280 mg) as a yellow solid. LRMS (ESI) m/z 302 (M+H).

Step 3: Preparation of 4-((3-(6-((pyridin-2-ylmethyl)amino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide. 2-Pyridinemethaneamine (145 mg, 1.34 mmol, 1.5 equiv) and 4-[[([6-oxospiro[3.3]heptan-2-yl]carbamoyl)amino]methyl]benzamide (270 mg, 0.90 mmol, 1.00 equiv) were dissolved in DCE (5 mL) and stirred at rt for 30 min before NaHB(OAc)₃ (285 mg, 1.34 mmol, 1.5 equiv) was added. After 1 h, the reaction was concentrated by rotary evaporation and product isolated by reverse phase HPLC (3%->15% MeCN/H2O w/ammonium formate) as a yellow solid (20 mg). LRMS (ESI) m/z 394 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.50 (d, J=4.9 Hz, 1H), 8.25 (s, 1H), 7.91 (s, 1H), 7.85-7.71 (m, 3H), 7.42 (d, J=7.9 Hz, 1H), 7.36-7.22 (m, 5H), 6.30 (t, J=6.2 Hz, 1H), 6.21 (d, J=8.0 Hz, 1H), 4.22 (d, J=6.0 Hz, 2H), 3.94 (q, J=7.9 Hz, 1H), 3.16 (p, J=7.7 Hz, 1H), 2.32-2.19 (m, 2H), 2.15 (dt, J=11.9, 6.4 Hz, 1H), 2.06 (dt, J=11.7, 5.9 Hz, 1H), 1.84-1.71 (m, 4H).

Example 15

Preparation of 4-((3-(6-((pyridin-2-ylmethyl)amino)spiro[3.3]heptan-2-yl)ureido)methyl)benzamide (Compound 187 and 182)

Preparation of 1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea. HATU (1.4 g, 3.7 mmol, 1.5 equiv) was added to a stirring solution of 6-(3-(4-chlorobenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (intermediate 2.1) (1 g, 0.36 mmol, 1 equiv), 2-methyl-1-(piperazin-1-yl)propan-2-ol (980 mg, 6.2 mmol, 2 equiv) and NEt₃ (1.3 mL, 9.3 mmol, 3 equiv) in EtOAc(50 mL) at rt. After 12 h, the reaction was dry loaded onto silica and racemic product isolated by silica chromatography (0->15% MeOH/CH2CL2 w/0.1% formic acid) as a white solid.

Chiral Separation of 1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea.

The 1 g mixture of 1-(4-chlorobenzyl)-3-(6-(4-(2-hydroxy-2-methylpropyl)piperazine-1-carbonyl)spiro[3.3]heptan-2-yl)urea was separated by SFC (Chiralcel OX-H column, 50% co-solvent [25% MeOH/MeCN w/0.25% isopropylamine] at 70 g/min) affording the two isomers Compound 187 (0.32 g, 46%) and Compound 182 (0.33 g, 47%) as white solids. The absolute stereochemistry of each isomer was not determined and arbitrarily assigned. Compound 187 elutes first from SFC using stated conditions, followed by Compound 182.

Compound 187: LRMS (APCI) m/z 464.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.32 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.5 Hz, 2H), 4.28 (s, 2H), 4.03 (p, J=8.0 Hz, 1H), 3.62-3.52 (m, 2H), 3.47-3.39 (m, 2H), 3.27 (q, J=8.6 Hz, 1H), 2.55 (ddt, J 18.0, 11.5, 5.1 Hz, 5H), 2.37-2.22 (m, 6H), 2.12 (ddd, J=11.5, 8.5, 3.2 Hz, 1H), 1.87 (ddd, J=36.9, 11.1, 8.6 Hz, 2H), 1.21 (s, 6H).

Compound 182: LRMS (APCI) m/z 464.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.31 (d, J=8.5 Hz, 2H), 7.26 (d, J=8.4 Hz, 2H), 4.28 (s, 2H), 4.03 (p, J=8.0 Hz, 1H), 3.57 (q, J=4.6 Hz, 2H), 3.43 (t, J=4.9 Hz, 2H), 3.27 (t, J=8.6 Hz, 1H), 2.54 (ddt, J=18.2, 11.7, 5.0 Hz, 5H), 2.38-2.21 (m, 6H), 2.21-2.07 (m, 1H), 1.87 (ddd, J=37.2, 11.2, 8.6 Hz, 2H), 1.21 (s, 6H).

Compounds in the following table were prepared in a similar manner as Compound 187 and 182, using the intermediates and reagents as listed.

Compound		Chiral
No.	Racemate	Column	Structure, Name and Data
229	1-(4- methoxy- benzyl)-3- (6- (1,2,3,4- tetrahydro- quinoline- 1- carbonyl) spiro[3.3] heptan-2- yl)urea	Chiralcel OX-H
			E1: 1-(4-methoxybenzyl)-3-((2S,4s,6S)-6-
			(1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434.1 (M + H). 1H NMR (400 MHz,
			Chloroform-d) δ 7.32 - 6.93 (m, 6H), 6.88 -
			6.78 (m, 2H), 4.86 (s, 1H), 4.25 (s, 2H), 4.00 (p,
			J = 7.4 Hz, 1H), 3.79 (s, 3H), 3.71 (s, 2H), 3.36
			(p, J = 8.4 Hz, 1H), 2.80 (s, 1H), 2.70 (s, 2H),
			2.48 - 2.28 (m, 4H), 2.11 (s, 1H), 1.93 (p, J =
			6.6 Hz, 3H), 1.75 (dd, J = 11.5, 8.4 Hz, 2H).
			E2: 1-(4-methoxybenzyl)-3-((2R,4r,6R)-6-
			(1,2,3,4-tetrahydroquinoline-1-
			carbonyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434.1 (M + H). 1H NMR (400 MHz,
			Chloroform-d) δ 7.34 - 6.96 (m, 6H), 6.87 (d, J =
			8.6 Hz, 2H), 4.73 (s, 1H), 4.29 (s, 2H), 4.09 -
			3.91 (m, 1H), 3.81 (s, 3H), 3.73 (s, 2H), 3.45-
			3.28 (m, 1H), 2.79-2.70 (m, 3H), 2.56 -2.30
			(m, 4H), 2.08 (d, J = 33.8 Hz, 1H), 1.94 (p, J =
			6.6 Hz, 3H), 1.77 (dd, J = 11.5, 8.5 Hz, 2H).
			n.b. - Stereochemistry assigned randomly and
			not confirmed by crystallography
249	N-((6-(3- (4- chlorobenzyl) ureido) spiro[3.3] heptan-2- yl)methyl)- 6- methyl- nicotinamide	Chiralpak AD-H
			E1: N-(((2S,4s,6S)-6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-2-
			yl)methyl)-6-methylnicotinamide. LRMS
			(APCI) m/z 427.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.86 (d, J = 2.4 Hz, 1 H), 8.54 (t, J =
			5.7 Hz, 1 H), 8.06 (dd, J = 8.1, 2.3 Hz, 1 H),
			7.38-7.32 (m, 3 H), 7.23 (d, J = 8.4 Hz, 2 H),
			6.25 (t, J = 6.1 Hz, 1 H), 6.17 (d, J = 8.1 Hz, 1
			H), 4.15 (d, J = 6.0 Hz, 2 H), 3.91 (h, J = 8.2
			Hz, 1 H), 3.26 (t, J = 6.5 Hz, 2 H), 2.51 (s, 3 H),
			2.38 (p, J = 6.7, 5.9 Hz, 1 H), 2.30 (ddd, J =
			10.8, 7.4, 5.2 Hz, 1 H), 2.19 (ddd, J = 12.3, 7.2,
			5.1 Hz, 1 H), 2.09 (ddd, J = 11.2, 8.0, 3.1 Hz, 1
			H), 1.95 (ddd, J = 11.3, 8.0, 3.1 Hz, 1 H), 1.82-
			1.73 (m, 3 H), 1.73-1.66 (m, 1 H).
			E2: N-(((2R,4r,6R)-6-(3-(4-
			chlorobenzyl)ureido)spiro[3.3]heptan-2-
			yl)methyl)-6-methylnicotinamide. LRMS
			(APCI) m/z 427.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.86 (d, J = 2.3 Hz, 1 H), 8.54 (t, J =
			5.7 Hz, 1 H), 8.06 (dd, J = 8.1, 2.3 Hz, 1 H),
			7.41-7.30 (m, 3 H), 7.23 (d, J = 8.4 Hz, 2 H),
			6.25 (t, J = 6.0 Hz, 1 H), 6.17 (d, J = 8.1 Hz, 1
			H), 4.15 (d, J = 6.0 Hz, 2 H), 3.91 (h, J = 8.1
			Hz, 1 H), 3.26 (t, J = 6.5 Hz, 2 H), 2.51 (s, 3H),
			2.38 (p, J = 7.4 Hz, 1 H), 2.35-2.24 (m, 1 H),
			2.19 (dt, J = 12.1, 6.6 Hz, 1 H), 2.09 (ddd, J =
			11.1, 8.0, 3.1 Hz, 1 H), 1.95 (ddd, J = 11.2, 8.0,
			3.1 Hz, 1 H), 1.83-1.73 (m, 3 H), 1.73-1.66 (m,
			1 H).
			n.b. - Stereochemistry assigned randomly and
			not confirmed by crystallography

Example 16

Preparation of 1-(4-chlorobenzyl)-3-(6-((4-methyl-3-oxopiperazin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea (Compound 238)

1-(4-Chlorobenzyl)-3-(6-((4-methyl-3-oxopiperazin-1-yl)methyl)spiro[3.3]heptan-2-yl)urea. NaBH(OAc)₃ (249 mg, 1.17 mmol, 2 equiv) was added to a stirring solution of 1-(4-chlorobenzyl)-3-(6-formylspiro[3.3]heptan-2-yl)urea (Intermediate 11.1, 180 mg, 0.587 mmol, 1 equiv) and 1-methylpiperazin-2-one (134 mg, 1.17 mmol, 2 equiv) in CH₂Cl₂ (2 mL) at rt. After 12 h, solvent was removed by rotary evaporation, the crude suspended in MeOH (3 mL), filtered through a 0.4 μm syringe filter, and product isolated by reverse phase HPLC (0->30% MeCN/water w/0.1% formic acid) as a white solid (60 mg, 25%). LRMS (ESI) m/z 405.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.20 (d, J=8.2 Hz, 2H), 7.14 (d, J=8.2 Hz, 2H), 4.16 (s, 2H), 3.90 (p, J=8.0 Hz, 1H), 3.25 (t, J=5.6 Hz, 2H), 2.97 (s, 2H), 2.83 (s, 3H), 2.60 (t, J=5.7 Hz, 2H), 2.42-2.28 (m, 4H), 2.20-2.08 (m, 2H), 1.96 (ddd, J=11.1, 7.0, 4.1 Hz, 1H), 1.81-1.73 (m, 1H), 1.73-1.57 (in, 3H).

Compounds in the following table were prepared in a similar manner as Compound 238, using the intermediates and reagents as listed.

Compound		Carbonyl
No.	Amine	Compound	Structure, Name and Data
239	(R)-3- (pyrrolidin- 2- yl)pyridine	Intermediate 11.1
			(R)-1-(4-chlorobenzyl)-3-(6-((2-(pyridin-3-
			yl)pyrrolidin-1-yl)methyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (ESI) m/z 439.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 8.44 (s, 1H),
			8.40 - 8.30 (m, 1H), 7.78 (t, J = 6.3 Hz, 1H),
			7.35 (dt, J = 8.0, 4.1 Hz, 1H), 7.19 (d, J = 8.2
			Hz, 2H), 7.13 (d, J = 8.2 Hz, 2H), 4.15 (s, 2H),
			3.85 (p, J = 7.2 Hz, 1H), 3.44 (t, J = 8.4 Hz,
			1H), 3.26 (t, J = 8.5 Hz, 1H), 2.52 - 2.10 (m,
			6H), 2.01 (ddq, J = 17.7, 12.2, 6.1, 5.5 Hz, 2H),
			1.95 - 1.78 (m, 3H), 1.69 (q, J = 8.3, 6.8 Hz,
			2H), 1.63 - 1.40 (m, 3H).
254	1-methyl- 3- phenylpi- perazine	Intermeidate 11.1
			1-(4-chlorobenzyl)-3-(6-((4-methyl-2-
			phenylpiperazin-1-
			yl)methyl)spiro[3.3]heptan-2-yl)urea. LRMS
			(ESI) m/z 467.1 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 7.32 - 7.21 (m, 6H), 7.21 -7.12
			(m, 3H), 6.14 (d, J = 3.4 Hz, 1H), 6.03 (dd, J =
			8.1, 2.9 Hz, 1H), 4.06 (d, J = 6.1 Hz, 2H), 3.82-
			3.67 (m, 1H), 3.08 (dd, J = 10.3, 3.0 Hz, 1H),
			2.85 (d, J = 10.9 Hz, 1H), 2.70-2.57 (m, 2H),
			2.52 (dt, J = 11.0, 2.6 Hz, 1H), 2.22 (ttd, J =
			16.2, 11.1, 10.0, 4.7 Hz, 3H), 2.07 (d, J = 7.9
			Hz, 4H), 2.03 - 1.88 (m, 2H), 1.78 (dp, J =
			10.4, 5.2, 4.5 Hz, 4H), 1.63 (ddd, J = 11.2, 8.8,
			3.3 Hz, 1H), 1.51 - 1.41 (m, 1H), 1.40-1.23
			(m, 1H).
241	Intermediate 12.2	methyl 4- oxopentanote
			1-(4-chlorobenzyl)-3-(6-((2-methyl-5-
			oxopyrrolidin-1-yl)methyl)spiro[3.3]heptan-
			2-yl)urea. LRMS (ESI) m/z 390.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 7.24 - 7.17
			(m, 2H), 7.17 - 7.09 (m, 2H), 4.16 (s, 2H), 3.90
			(h, J = 8.1 Hz, 1H), 3.67 - 3.59 (m, 2H), 3.52-
			3.39 (m, 1H), 2.89 (dd, J = 13.8, 6.8 Hz, 1H),
			2.34 (p, J = 6.9 Hz, 2H), 2.21 (td, J = 11.9,
			11.4, 6.3 Hz, 2H), 2.15 - 1.98 (m, 2H), 1.80 -
			1.73 (m, 3H), 1.70- 1.57 (m, 2H), 1.54-1.41
			(m, 1H), 1.11 (d, J = 6.2 Hz, 3H).
244	Intermediate 12.2	methyl 2- methyl-4- oxobutanoate
			1-(4-chlorobenzyl)-3-(6-((3-methyl-2-
			oxopyrrolidin-1-yl)methyl)spiro[3.3]heptan-
			2-yl)urea. LRMS (ESI) m/z 390.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 7.31 (d, J =
			7.9 Hz, 2H), 7.26 (d, J = 8.2 Hz, 2H), 4.28 (s,
			2H), 4.02 (p, J = 7.7 Hz, 1H), 3.36 (d, J = 3.0
			Hz, 1H), 3.32 - 3.19 (m, 3H), 2.46 (dq, J =
			15.4, 7.5, 7.1 Hz, 3H), 2.38 - 2.14 (m, 3H),
			2.03 (ddd, J = 11.3, 7.8, 3.3 Hz, 1H), 1.84 (dt, J =
			17.6, 8.8 Hz, 3H), 1.78 - 1.69 (m, 1H), 1.63
			(dq, J = 16.9, 8.3 Hz, 1H), 1.17 (d, J = 7.1 Hz,
			3H).
253	1- methylpi- perazin-2- one	Intermediate 15.1
			1-(4-chlorobenzyl)-3-(6-(1-(4-methyl-3-
			oxopiperazin-1-yl)ethyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (ESI) m/z 419.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 7.31 (d, J =
			8.3 Hz, 2H), 7.26 (d, J = 8.3 Hz, 2H), 4.28 (s,
			2H), 4.02 (p, J = 7.2 Hz, 1H), 3.47 -3.11 (m,
			7H), 2.93 - 2.86 (m, 1H), 2.78 (dq, J = 12.2, 5.8
			Hz, 1H), 2.63 (dq, J = 12.6, 6.2 Hz, 1H), 2.50
			(dt, J = 11.6, 6.5 Hz, 1H), 2.30 (dd, J = 16.9,
			8.4 Hz, 1H), 2.20 (tq, J = 12.0, 4.6, 3.8 Hz, 2H),
			2.07 - 1.94 (m, 1H), 1.88 (ddt, J = 12.2, 9.0, 4.8
			Hz, 2H), 1.75 (dq, J = 19.5, 10.7 Hz, 2H), 0.95
			(t, J = 6.0 Hz, 3H).

Example 17

Preparation of 1-(4-chlorobenzyl)-3-(6-((5-phenyl-1H-1,2,3-triazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea (Compound 242)

1-(4-Chlorobenzyl)-3-(6-((5-phenyl-1H-1,2,3-triazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea. 1-(6-(Azidomethyl)spiro[3.3]heptan-2-yl)-3-(4-chlorobenzyl)urea (100 mg, 0.30 mmol, 1 equiv), ethynylbenzene (46 mg, 0.449 mmol, 1.5 equiv), and Cp*RuCl(cod) (11 mg, 0.03 mmol, 0.1 equiv) were suspended in THF (5 mL) before being heated to 60° C. After 12 h, the reaction was cooled to rt, solvent removed by rotary evaporation, and product isolated by reverse phase HPLC (5->95% MeCN/water 0.1% formic acid) as a white solid (20 mg, 15%). LRMS (ESI) m/z 436.1 (M+H). ¹H NMR (400 MHz, Chloroform-d) δ 7.10 (d, J=5.5 Hz, 3H), 6.99-6.92 (m, 2H), 6.88 (d, J=10.0 Hz, 5H), 6.81 (d, J=8.0 Hz, 2H), 4.28 (t, J=5.9 Hz, 1H), 4.19 (d, J=7.4 Hz, 1H), 3.92 (d, J=6.5 Hz, 4H), 3.64-3.50 (m, 1H), 2.24 (dt, J=15.3, 7.5 Hz, 1H), 2.02 (dt, J=11.9, 6.4 Hz, 1H), 1.83 (dt, J=12.1, 6.4 Hz, 1H), 1.74-1.65 (m, 1H), 1.60-1.47 (m, 3H).

Example 18

Preparation of 1-(4-(1-(2H-tetrazol-5-yl)piperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea (Compound 318)

Step 1: 1-(4-Chlorobenzyl)-3-(4-(1-cyanopiperidin-4-yl)butyl)urea. CNBr (154 mg, 1.46 mmol, 1.05 equiv) was added to a stirring solution of 1-(4-chlorobenzyl)-3-(4-(piperidin-4-yl)butyl)urea (Intermediate 3.8, 500 mg, 1.39 mmol, 1 equiv) and saturated sodium bicarbonate (4.2 mL) in CH₂Cl₂ (10 mL) at 0° C. After 14 h, the reaction was extracted with CH₂Cl₂ (3×5 mL), organics combined, dried over sodium sulfate, filtered through a pad of silica, and solvent removed by rotary evaporation to give the crude product which was used in the next step without further purification (267 mg, 55%). LRMS (ESI) m/z 349.1 (M+H).

Step 2: 1-(4-(1-(2H-tetrazol-5-yl)piperidin-4-yl)butyl)-3-(4-chlorobenzyl)urea.

• 1-(4-Chlorobenzyl)-3-(4-(1-cyanopiperidin-4-yl)butyl)urea (102 mg, 0.29 mmol, 1 equiv), sodium azide (21 mg, 0.322 mmol, 1.1 equiv), and zinc bromide (66 mg, 0.293 mmol, 1 equiv), were suspended in DMF (2 mL) before being heated to 100° C. for 3 h. The reaction was cooled to rt and product isolated by reverse phase HPLC (10->60% MeCN/water w/0.1% formic acid) as a white solid. LRMS (ESI) m/z 392.1 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 7.37 (d, J=8.0 Hz, 2H), 7.26 (d, J=8.0 Hz, 2H), 6.31 (t, J=6.1 Hz, 1H), 5.93 (t, J=5.6 Hz, 1H), 4.18 (d, J=5.9 Hz, 2H), 3.80 (d, J=12.7 Hz, 2H), 3.05-2.90 (m, 4H), 1.71 (d, J=14.1 Hz, 2H), 1.36 (t, J=7.0 Hz, 3H), 1.32-1.07 (m, 7H).

Example 19

Preparation of 1-(4-methoxybenzyl)-3-(6-(5-phenyl-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)urea (Compound 325)

1-(4-Methoxybenzyl)-3-(6-(5-phenyl-1,3,4-oxadiazol-2-yl)spiro[3.3]heptan-2-yl)urea. 6-(3-(4-Methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (200 mg, 0.628 mmol, 1 equiv) and benzohydrazide (86 mg, 0.628 mmol, 1 equiv) were suspended in phosphorus oxychloride (5 mL) before being stirred at rt for 14 h. The solvent was removed by rotary evaporation and product isolated by reverse phase HPLC (5->95% MeCN/water w/0.1% formic acid) as a white solid (17 mg, 5%). LRMS (ESI) m/z 419.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 8.04 (d, J=8.3 Hz, 2H), 7.59 (q, J=7.5, 6.5 Hz, 3H), 7.20 (d, J=8.1 Hz, 2H), 6.88 (d, J=7.1 Hz, 2H), 4.24 (s, 2H), 4.10 (p, J=8.0 Hz, 1H), 3.78 (s, 4H), 2.71-2.53 (m, 3H), 2.47 (dd, J=21.5, 7.2 Hz, 3H), 1.98 (dt, J=23.2, 10.0 Hz, 2H).

Example 20

Preparation of 1-(4-methoxybenzyl)-3-(6-(4-phenyloxazol-2-yl)spiro[3.3]heptan-2-yl)urea (Compound 326)

1-(4-Methoxybenzyl)-3-(6-(4-phenyloxazol-2-yl)spiro[3.3]heptan-2-yl)urea. DCC (143 mg, 0.693 mmol, 1.05 equiv) was added to a stirring solution of 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (210 mg, 0.660 mmol, 1 equiv), 2-hydroxy-1-phenylethan-1-one (90 mg, 0.660 mmol, 1 equiv), and DMAP (1 mg, 0.007 mmol, 0.01 equiv) in CH₂Cl₂ (20 mL) at rt. After 14 h, the reaction was filtered through a pad of celite and solvent removed by rotary evaporation. The crude material was suspended in toluene (50 mL) before ammonium acetate (101 mg, 1.32 mmol, 2 equiv) and AcOH (2 mL) were added and the reaction heated to reflux for 2 h. The reaction was cooled to rt, solvent removed by rotary evaporation, and product isolated by reverse phase HPLC (5->95% MeCN/water w/0.1% formic acid) as a white solid (55 mg, 20%). LRMS (ESI) m/z 418.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 8.15 (s, 1H), 7.73 (d, J=7.7 Hz, 2H), 7.41 (t, J=7.6 Hz, 2H), 7.32 (t, J=7.4 Hz, 1H), 7.21 (d, J=8.2 Hz, 2H), 6.88 (d, J=8.2 Hz, 2H), 4.24 (s, 2H), 4.09 (p, J=8.1 Hz, 1H), 3.78 (s, 3H), 3.61 (p, J=8.6 Hz, 1H), 2.61 (dt, J=11.5, 5.7 Hz, 1H), 2.57-2.48 (m, 2H), 2.48-2.33 (m, 3H), 2.04-1.95 (m, 1H), 1.95-1.85 (m, 1H).

Example 21

Preparation of 1-(6-(benzo[d]oxazol-2-yl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea (Compound 327)

1-(6-(Benzo[d]oxazol-2-yl)spiro[3.3]heptan-2-yl)-3-(4-methoxybenzyl)urea. DCC (136 mg, 0.660 mmol, 1.05 equiv) was added to a stirring solution of 6-(3-(4-methoxybenzyl)ureido)spiro[3.3]heptane-2-carboxylic acid (200 mg, 0.628 mmol, 1 equiv), 2-aminophenol (75 mg, 0.691 mmol, 1 equiv), and DMAP (1 mg, 0.007 mmol, 0.01 equiv) in CH₂Cl₂ (20 mL) at rt. After 14 h, the reaction was filtered through a pad of celite and solvent removed by rotary evaporation. The crude material was suspended in toluene (20 mL) before 4-methylbenzenesulfonic acid (11 mg, 0.063 mmol, 0.1 equiv) was added and the reaction heated to reflux for 2 h. The reaction was cooled to rt, solvent removed by rotary evaporation, and product isolated by reverse phase HPLC (5->95% MeCN/water w/0.1% formic acid) as a white solid (35 mg, 14%). LRMS (ESI) m/z 392.1 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.68-7.53 (m, 2H), 7.41-7.32 (m, 2H), 7.20 (d, J=7.6 Hz, 2H), 6.88 (d, J=7.5 Hz, 2H), 4.24 (s, 2H), 4.10 (p, J=8.4, 7.7 Hz, 1H), 3.83-3.67 (m, 4H), 2.70-2.35 (m, 6H), 1.97 (dt, J=33.1, 10.0 Hz, 2H).

Example 22

Preparation of 1-(4-chlorobenzyl)-3-(6-(hydroxy(phenyl)methyl)spiro[3.3]heptan-2-yl)urea (Compound 328)

1-(4-Chlorobenzyl)-3-(6-(hydroxy(phenyl)methyl)spiro[3.3]heptan-2-yl)urea. Phenylmagnesium bromide (1 M in THF, 652 mL, 0.652 mmol, 2 equiv) was added to a stirring solution of 1-(4-chlorobenzyl)-3-(6-formylspiro[3.3]heptan-2-yl)urea (Intermediate 11.1, 100 mg, 0.326 mmol, 1 equiv) in THF (5 mL) at 0° C. After 2 h, the reaction was quenched with saturated ammonium chloride (50 mL), extracted with CH₂Cl₂ (3×25 mL), organics combined, dried over sodium sulfate, filtered, and solvent removed by rotary evaporation. The product was isolated by reverse phase HPLC (5->95% MeCN/water w/0.1% formic acid) as a white solid (13 mg, 10%). LRMS (ESI) m/z 385.2 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.34-6.94 (m, 9H), 4.32 (d, J=8.3 Hz, 1H), 4.16 (s, 2H), 3.88 (dt, J=17.2, 8.3 Hz, 2H), 2.34 (dt, J=15.8, 7.8 Hz, 2H), 2.19-2.05 (m, 2H), 1.99-1.83 (m, 2H), 1.79-1.58 (m, 4H).

Compounds in the following table were prepared in a similar manner as Compound 328, using the intermediates and reagents as listed.

Compound
No.	Intermediate	Grignard	Structure, Name and Data
338	Intermediate 14.1	(6- methylpyridin- 3- yl)magnesium bromide
			1-(4-chlorobenzyl)-3-(6-(1-hydroxy-1-
			(6-methylpyridin-3-
			yl)ethyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 414.1 (M + H). 1H
			NMR (400 MHz, Methanol-d4) δ 8.47
			(s, 1H), 7.77 (d, J = 8.2 Hz, 1H), 7.31
			(d, J = 8.1 Hz, 2H), 7.25 (d, J = 8.0 Hz,
			3H), 4.27 (s, 2H), 3.99 (dt, J = 22.2, 7.9
			Hz, 1H), 3.37 (s, 1H), 2.65 - 2.54 (m,
			1H), 2.51 (s, 3H), 2.44 (tt, J = 11.4, 5.8
			Hz, 1H), 2.19 (dt, J = 11.6, 5.7 Hz, 1H),
			2.10 (dd, J = 20.2, 9.7 Hz, 1H), 1.95
			(dd, J = 18.3, 8.3 Hz, 1H), 1.85 (dd, J =
			19.0, 9.5 Hz, 1H), 1.74 (td, J = 21.3,
			19.1, 8.8 Hz, 2H), 1.42 (d, J = 4.1 Hz,
			3H).

Example 23

Preparation of 1-(4-methoxybenzyl)-3-(6-(4-methylbenzyl)spiro[3.3]heptan-2-yl)urea (Compound 334)

1-(4-Methoxybenzyl)-3-(6-(4-methylbenzyl)spiro[3.3]heptan-2-yl)urea. (6-(3-(4-Methoxybenzyl)ureido)spiro[3.3]heptan-2-yl)methyl 4-methylbenzenesulfonate (Intermediate 19.1, 100 mg, 0.218 mmol, 1 equiv), 1-bromo-4-methylbenzene (56 mg, 0.327 mmol, 1.5 equiv), tetrabutylammonium iodide (121 mg, 0.327 mmol, 1.5 equiv), zinc (43 mg, 0.654 mmol, 3 equiv), and Ni precatalyst (as prepared in: Mennie, Katrina; Vara, Brandon; Levi, Samuel. Reductive sp3-sp2 Coupling Reactions Enable Late-Stage Modification of Pharmaceuticals. Organic Letters. 2020, 22, 556-559) (6 mg, 0.011 mmol, 0.05 equiv) were placed under cycling N2 for 5 min before MeCN (5 mL) was added, the vial sealed, and the reaction heated to 90° C. After 14 h, the reaction was cooled to rt, solvent removed by rotary evaporation, and product isolated by reverse phase HPLC (5->95% MeCN/water w/0.1% formic acid) as a white solid. LRMS (ESI) m/z 379.2 (M+H). ¹H NMR (400 MHz, Methanol-d₄) δ 7.19 (d, J=8.2 Hz, 2H), 7.06 (d, J=7.7 Hz, 2H), 7.00 (d, J=7.7 Hz, 2H), 6.87 (d, J=8.1 Hz, 2H), 4.22 (s, 2H), 4.01 (p, J=8.1 Hz, 1H), 3.78 (s, 3H), 2.61 (d, J=7.6 Hz, 2H), 2.41 (dq, J=15.4, 7.7, 6.9 Hz, 2H), 2.29 (s, 4H), 2.15 (t, J=10.0 Hz, 1H), 2.02-1.92 (m, 1H), 1.81 (dd, J=16.7, 7.6 Hz, 3H), 1.75-1.66 (m, 1H).

Compounds in the following table were prepared in a similar manner as Compound 334, using the intermediates and reagents as listed.

Compound		Aryl
No.	Intermediate	Bromide	Structure, Name and Data
335	Intermediate 19.1	1-bromo-3- methylbenzene
			1-(4-Methoxybenzyl)-3-(6-(3-
			methylbenzyl)spiro[3.3]heptan-2-yl)urea
			LRMS (ESI) m/z 379.1 (M + H). 1H NMR
			(400 MHz, Methanol-d4) δ 7.19 (d, J = 8.1
			Hz, 2H), 7.12 (t, J = 7.5 Hz, 1H), 7.00 -
			6.89 (m, 3H), 6.87 (d, J = 8.1 Hz, 2H), 4.22
			(s, 2H), 4.00 (q, J = 8.0 Hz, 1H), 3.78 (s,
			3H), 2.62 (d, J = 7.6 Hz, 2H), 2.42 (p, J =
			8.8 Hz, 2H), 2.30 (s, 4H), 2.22 - 2.10 (m,
			1H), 2.04 - 1.91 (m, 1H), 1.81 (q, J = 10.7
			Hz, 3H), 1.76 - 1.66 (m, 1H).
336	Intermediate 19.1	1-bromo-2- methylbenzene
			1-(4-methoxybenzyl)-3-(6-(2-
			methylbenzyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 379.1 (M + H). 1H NMR
			(400 MHz, Methanol-d4) δ 7.19 (d, J = 8.1
			Hz, 2H), 7.10 (d, J = 7.1 Hz, 1H), 7.06 (s,
			3H), 6.90 - 6.83 (m, 2H), 4.22 (s, 2H), 4.01
			(d, J = 7.9 Hz, 1H), 3.78 (d, J = 1.3 Hz,
			3H), 2.68 (d, J = 7.4 Hz, 2H), 2.46 (dq, J =
			13.4, 7.0, 6.3 Hz, 2H), 2.28 (s, 4H), 2.19
			(dt, J = 11.2, 5.7 Hz, 1H), 2.06 - 1.95 (m,
			1H), 1.82 (q, J = 10.2 Hz, 3H), 1.78 - 1.69
			(m, 1H).
331	Intermeidate 19.2	2- bromopyrazine
			1-(4-chlorobenzyl)-3-(6-(pyrazin-2-
			ylmethyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 371.1 (M + H). 1H NMR
			(400 MHz, Methanol-d4) δ 8.48 - 8.25 (m,
			3H), 7.19 (d, J = 8.5 Hz, 2H), 7.13 (d, J =
			8.4 Hz, 2H), 4.16 (s, 2H), 3.90 (p, J = 8.2
			Hz, 1H), 2.79 (d, J = 7.8 Hz, 2H), 2.51 (dq,
			J = 16.0, 8.0 Hz, 1H), 2.34 (dt, J = 11.6, 6.6
			Hz, 1H), 2.18 (dt, J = 12.1, 6.7 Hz, 1H),
			2.09 (ddd, J = 11.6, 7.8, 4.1 Hz, 1H), 1.91
			(ddd, J = 11.8, 7.7, 4.1 Hz, 1H), 1.81 - 1.64
			(m, 4H).
337	Intermediate 19.1	5-bromo-2- methylpyridine
			1-(4-methoxybenzyl)-3-(6-((6-
			methylpyridin-3-
			yl)methyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 380.1 (M + H). 1H NMR
			(400 MHz, Methanol-d4) δ 8.20 (s, 1H),
			7.55 (d, J = 8.0 Hz, 1H), 7.23 (d, J = 8.0 Hz,
			1H), 7.19 (d, J = 8.1 Hz, 2H), 6.91 - 6.81
			(m, 2H), 4.22 (s, 2H), 4.02 (p, J = 7.9 Hz,
			1H), 3.77 (d, J = 1.5 Hz, 3H), 2.67 (d, J =
			7.7 Hz, 2H), 2.50 (s, 3H), 2.42 (d, J = 7.5
			Hz, 2H), 2.28 (dt, J = 12.3, 6.3 Hz, 2H),
			2.18 (td, J = 9.7, 8.1, 4.0 Hz, 1H), 2.00
			(ddd, J = 11.6, 7.6, 4.0 Hz, 1H), 1.82 (q, J =
			10.8, 10.3 Hz, 3H), 1.77 - 1.69 (m, 1H).
345	Intermediate 19.2	3- bromopyridine
			1-(4-chlorobenzyl)-3-(6-(pyridin-3-
			ylmethyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 370.2 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.38 (s, 1H), 7.56
			(dt, J = 7.8, 2.0 Hz, 1H), 7.41-7.32 (m,
			2H), 7.28 (dd, J = 7.8, 4.7 Hz, 1H), 7.23 (d,
			J = 8.4 Hz, 2H), 6.24 (t, J = 6.1 Hz, 1H),
			6.17 (d, J = 8.0 Hz, 1H), 4.14 (d, J = 6.0 Hz,
			2H), 3.90 (h, J = 8.1 Hz, 1H), 2.64 (dd, J =
			7.6, 1.9 Hz, 2H), 2.43 - 2.24 (m, 3H), 2.16
			(dt, J = 12.1, 6.2 Hz, 1H), 2.08 (ddd, J =
			11.2, 7.6, 3.9 Hz, 1H), 1.92 (ddd, J = 11.5,
			7.7, 3.9 Hz, 1H), 1.81 - 1.70 (m, 3H), 1.68
			(dd, J = 11.2, 8.1 Hz, 1H).
346	Intermediate 19.2	3-iodo-2- methylpyridine
			1-(4-chlorobenzyl)-3-(6-((2-
			methylpyridin-3-
			yl)methyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 384.2 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.25 (dd, J = 4.8,
			1.7 Hz, 1H), 7.43 (dd, J = 7.7, 1.7 Hz, 1H),
			7.36 (d, J = 8.4 Hz, 2H), 7.23 (d, J = 8.4 Hz,
			2H), 7.11 (dd, J = 7.6, 4.8 Hz, 1H), 6.24 (t,
			J = 6.0 Hz, 1H), 6.17 (d, J = 8.0 Hz, 1H),
			4.15 (d, J = 6.0 Hz, 2H), 3.91 (h, J = 8.2 Hz,
			1H), 2.64 (d, J = 7.5 Hz, 2H), 2.42 (s, 3H),
			2.32 (s, 1H), 2.22 - 2.07 (m, 3H), 1.95 (ddd,
			J = 11.5, 7.7, 4.0 Hz, 1H), 1.76 (q, J = 9.7
			Hz, 3H), 1.68 (dd, J = 11.2, 8.2 Hz, 1H).
347	Intermeidate 19.2	5-bromo-2- methylpyridine
			1-(4-chlorobenzyl)-3-(6-((6-
			methylpyridin-3-
			yl)methyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (ESI) m/z 384.2 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.22 (d, J = 2.2 Hz,
			1H), 7.44 (dd, J = 7.9, 2.3 Hz, 1H), 7.41-
			7.31 (m, 2H), 7.23 (d, J = 8.3 Hz, 2H), 7.13
			(d, J = 7.9 Hz, 1H), 6.27 (s, 1H), 6.19 (d, J =
			8.1 Hz, 1H), 4.14 (d, J = 5.9 Hz, 2H), 3.90
			(td, J = 15.9, 8.0 Hz, 1H), 2.64 - 2.56 (m,
			2H), 2.41 (s, 3H), 2.34 - 2.23 (m, 2H), 2.19 -
			2.12 (m, 1H), 2.07 (ddd, J = 11.4, 7.8, 3.9
			Hz, 1H), 1.91 (ddd, J = 11.5, 7.7, 3.9 Hz,
			1H), 1.80 - 1.68 (m, 3H), 1.65 (dd, J = 11.2,
			8.1 Hz, 1H).

Example 24

Preparation of 1-(4-chlorobenzyl)-3-(6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)urea (Compound 329)

1-(4-Chlorobenzyl)-3-(6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)urea. To a solution of 6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-amine (Intermediate 22.1) (75 mg, 0.37 mmol, 1.0 equiv) in CH₂Cl₂ (1 mL) was added Et₃N (75 mg, 0.74 mmol, 2.0 equiv) and 1-chloro-4-(isocyanatomethyl)benzene (93 mg, 0.56 mmol, 1.5 equiv) at 23° C. The reaction was stirred at this temperature for 30 min before it was directly concentrated and purified by preparative HPLC (H₂O (0.1% HCO₂H)/MeCN (0.1% HCO₂H)) to yield 1-(4-chlorobenzyl)-3-(6-(pyridin-4-ylmethyl)spiro[3.3]heptan-2-yl)urea (70 mg, 51%) as a colorless oil. LRMS (APCI+) m/z 370.10 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.48 (s, 2H), 7.35 (d, J=8.4 Hz, 2H), 7.30-7.17 (m, 4H), 6.25 (t, J=6.1 Hz, 1H), 6.17 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.0 Hz, 2H), 3.90 (h, J=8.1 Hz, 1H), 2.68 (dd, J=7.6, 1.8 Hz, 2H), 2.40 (p, J=7.9 Hz, 1H), 2.30 (ddd, J 10.18, 7.3, 5.2 Hz, 1H), 2.17 (ddd, J 12.1, 7.3, 5.2 Hz, 1H), 2.09 (ddd, J J 11.3, 7.7, 3.9 Hz, 1H), 1.93 (ddd, J 11.6, 7.7, 4.0 Hz, 1H), 1.75 (q, J 9.0 Hz, 3H), 1.68 (dd, J=11.2, 8.2 Hz, 1H).

Compounds in the following table were prepared in a similar manner as Compound 329, using the intermediates and reagents as listed.

Compound
No.	Isocyanate	Intermediate	Structure, Name and Data
330	1-methoxy- 4- (isocyanato- methyl)ben- zene	22.1
			1-(4-methoxybenzyl)-3-(6-(pyridin-4-
			ylmethyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 366.15 (M + H). 1H
			NMR (400 MHz, DMSO-d6) δ 8.46 (s, 2 H),
			7.18 (s, 2 H), 7.14 (d, J = 8.6 Hz, 2 H), 6.86
			(d, J = 8.6 Hz, 2 H), 6.15-6.03 (m, 2H),
			4.08 (d, J = 5.9 Hz, 2 H), 3.91 (h, J = 8.2
			Hz, 1 H), 3.72 (s, 3 H), 2.64 (dd, J = 7.7, 2.4
			Hz, 2 H), 2.40 (dq, J = 15.8, 7.8 Hz, 1 H),
			2.30 (ddd, J = 10.6, 7.4, 5.2 Hz, 1 H), 2.16
			(ddd, J = 12.2, 7.3, 5.2 Hz, 1 H), 2.10 (ddd,
			J = 11.2, 7.7, 3.9 Hz, 1 H), 1.93 (ddd, J =
			11.6, 7.7, 3.9 Hz, 1 H), 1.79-1.63 (m, 4 H).
332	1-chloro-4- (isocyanato- methyl)benzene	23.1
			1-(4-chlorobenzyl)-3-(6-(5-(6-
			methylpyridin-3-yl)-1,3,4-oxadiazol-2-
			yl)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 434.2 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 9.02 (d, J = 2.2 Hz, 1
			H), 8.23 (dd, J = 8.1, 2.3 Hz, 1 H), 7.49 (d,
			J = 8.1 Hz, 1 H), 7.37 (d, J = 8.5 Hz, 2 H),
			7.25 (d, J = 8.4 Hz, 2 H), 6.30 (t, J = 6.1 Hz,
			1 H), 6.23 (d, J = 8.0 Hz, 1 H), 4.16 (d, J =
			6.0 Hz, 2 H), 3.97 (h, J = 8.2 Hz, 1 H), 3.72
			(p, J = 8.3 Hz, 1 H), 2.57 (s, 3 H), 2.53 (d, J =
			8.4 Hz, 1 H), 2.49-2.43 (m, 2 H), 2.40 (d,
			J = 8.4 Hz, 2 H), 2.29 (ddd, J = 12.2, 7.4,
			5.2 Hz, 1 H), 1.91 (dd, J = 10.8, 8.7 Hz, 1
			H), 1.85 (dd, J = 11.1, 8.8 Hz, 1 H).
340	1-chloro-4- (isocyanato- methyl)benzene	24.1
			1-(4-chlorobenzyl)-3-(6-(pyrimidin-2-
			ylmethyl)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 371.10 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.69 (d, J = 4.8 Hz,
			2 H), 7.36 (d, J = 8.1 Hz, 2 H), 7.31 (t, J =
			4.9 Hz, 1 H), 7.23 (d, J = 8.1 Hz, 2 H), 6.25
			(t, J = 6.1 Hz, 1 H), 6.17 (d, J = 8.0 Hz, 1
			H), 4.15 (s, 2 H), 3.90 (h, J = 8.1 Hz, 1 H),
			2.92 (d, J = 7.6 Hz, 2 H), 2.64 (hept, J = 7.9
			Hz, 1 H), 2.31 (ddd, J = 11.3, 7.2, 5.2 Hz, 1
			H), 2.22-2.06 (m, 2 H), 1.97 (ddd, J = 11.5,
			7.8, 3.7 Hz, 1 H), 1.83-1.67 (m, 4 H).
341	1-chloro-4- (isocyanato- methyl)ben- zene	25.1
			1-(4-chlorobenzyl)-3-(6-(pyridin-4-
			yloxy)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 372.10 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.35 (d, J = 5.4 Hz, 2
			H), 8.14 (s, 1 H), 7.36 (d, J = 8.4 Hz, 2 H),
			7.24 (d, J = 8.4 Hz, 2 H), 6.86 (d, J = 6.5
			Hz, 2 H), 6.28 (t, J = 6.1 Hz, 1 H), 4.71 (p, J =
			6.9 Hz, 1 H), 4.16 (d, J = 6.0 Hz, 2 H),
			3.98 (h, J = 8.0 Hz, 1 H), 2.65 (dt, J = 11.5,
			6.0 Hz, 1 H), 2.48 (p, J = 5.7, 5.2 Hz, 1 H),
			2.38 (ddd, J = 10.9, 7.4, 5.2 Hz, 1 H), 2.24
			(ddd, J = 12.4, 7.5, 5.1 Hz, 1 H), 2.06 (ddd,
			J = 14.3, 11.6, 7.0 Hz, 2 H), 1.88 (ddd, J =
			11.1, 8.8, 5.8 Hz, 2 H).
343	1-chloro-4- (isocyanato- methyl)ben- zene	25.2
			1-(4-chlorobenzyl)-3-(6-(pyridin-3-
			yloxy)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 372.10 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.23-8.11 (m, 2 H), 7.36
			(d, J = 8.4 Hz, 2 H), 7.33-7.21 (m, 4 H),
			6.28 (t, J = 6.1 Hz, 1 H), 6.23 (d, J = 8.0 Hz,
			1 H), 4.68 (p, J = 6.9 Hz, 1 H), 4.16 (d, J =
			6.0 Hz, 2 H), 3.98 (h, J = 8.2 Hz, 1 H), 2.64
			(dt, J = 11.5, 5.9 Hz, 1 H), 2.46 (p, J = 5.9
			Hz, 1 H), 2.38 (ddd, J = 10.8, 7.4, 5.1 Hz, 1
			H), 2.24 (ddd, J = 12.1, 7.3, 5.2 Hz, 1 H),
			2.05 (td, J = 12.3, 7.0 Hz, 2 H), 1.88 (ddd, J =
			11.1, 8.7, 4.3 Hz, 2 H).
342	1-chloro-4- (isocyanato- methyl)ben- zene	26.1
			1-(4-chlorobenzyl)-3-(6-
			(methylsulfonyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 357.10 (M + H).
			1H NMR (400 MHz, DMSO-d6) δ 7.36 (d, J =
			8.4 Hz, 2 H), 7.24 (d, J = 8.4 Hz, 2 H),
			6.29 (t, J = 6.2 Hz, 1 H), 6.21 (d, J = 8.0 Hz,
			1 H), 4.15 (d, J = 6.0 Hz, 2 H), 3.93 (h, J =
			8.0 Hz, 1H), 3.86 (p, J = 8.3 Hz, 1H), 2.82
			(s, 3 H), 2.42-2.11 (m, 6 H), 1.86 (dd, J =
			10.9, 8.7 Hz, 1 H), 1.80 (dd, J = 11.2, 8.8
			Hz, 1 H).
344	1-methoxy- 4- (isocyanato- methyl)ben- zene	25.2
			1-(4-methoxybenzyl)-3-(6-(pyridin-3-
			yloxy)spiro[3.3]heptan-2-yl)urea. LRMS
			(APCI) m/z 372.10 (M + H). 1H NMR (400
			MHz, DMSO-d6) δ 8.19 (s, 1 H), 8.15 (d, J =
			4.1 Hz, 1 H), 7.36-7.23 (m, 2 H), 7.15 (d,
			J = 8.6 Hz, 2 H), 6.86 (d, J = 8.6 Hz, 2 H),
			6.18-6.08 (m, 2 H), 4.68 (p, J = 6.9 Hz, 1
			H), 4.10 (d, J = 5.9 Hz, 2 H), 3.99 (h, J =
			8.2 Hz, 1 H), 3.72 (s, 3H), 2.64 (dt, J =
			11.5, 5.9 Hz, 1 H), 2.46 (p, J = 5.9 Hz, 1 H),
			2.38 (ddd, J = 10.8, 7.4, 5.2 Hz, 1 H), 2.24
			(ddd, J = 12.1, 7.4, 5.2 Hz, 1 H), 2.13-1.99
			(m, 2 H), 1.92-1.82 (m, 2 H).
348	1-chloro-4- (isocyanato- methyl)ben- zene	27.1
			1-(4-chlorobenzyl)-3-(6-(pyridin-4-
			ylmethoxy)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 386.10 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.53 (s, 2 H), 7.36
			(d, J = 8.4 Hz, 2 H), 7.31 (d, J = 4.9 Hz, 2
			H), 7.24 (d, J = 8.4 Hz, 2 H), 6.26 (t, J = 6.1
			Hz, 1 H), 6.19 (d, J = 8.0 Hz, 1 H), 4.38 (s,
			2 H), 4.15 (d, J = 5.9 Hz, 2 H), 4.01-3.89
			(m, 2 H), 2.36 (dt, J = 11.4, 5.9 Hz, 1 H),
			2.30-2.12 (m, 3 H), 1.91 (td, J = 11.8, 7.3
			Hz, 2 H), 1.81 (q, J = 10.5, 10.0 Hz, 2 H).
349	1-methoxy- 4- (isocyanato- methyl)ben- zene	27.1
			1-(4-methoxybenzyl)-3-(6-(pyridin-4-
			ylmethoxy)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 382.20 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.53 (s, 2 H), 7.31
			(d, J = 4.8 Hz, 2 H), 7.14 (d, J = 8.6 Hz, 2
			H), 6.86 (d, J = 8.6 Hz, 2 H), 6.18-6.06 (m,
			2 H), 4.38 (s, 2 H), 4.09 (d, J = 5.9 Hz, 2
			H), 3.94 (dq, J = 13.7, 7.5, 6.8 Hz, 2 H),
			3.72 (s, 3 H), 2.36 (dt, J = 11.4, 5.9 Hz, 1
			H), 2.29-2.21 (m, 1 H), 2.18 (dt, J = 11.1,
			6.0 Hz, 2 H), 1.90 (ddd, J = 13.7, 11.2, 7.3
			Hz, 2 H), 1.85-1.74 (m, 2 H).
350	1-chloro-4- (isocyanato- methyl)ben- zene	27.2
			1-(4-chlorobenzyl)-3-(6-(pyridin-3-
			ylmethoxy)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 386.15 (M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.64-8.41 (m, 2
			H), 7.72 (d, J = 7.8 Hz, 1 H), 7.43-7.32 (m,
			3 H), 7.24 (d, J = 8.4 Hz, 2 H), 6.27 (t, J =
			6.1 Hz, 1 H), 6.20 (d, J = 8.0 Hz, 1 H), 4.37
			(s, 2 H), 4.15 (d, J = 6.0 Hz, 2 H), 3.93 (dq,
			J = 14.1, 7.5, 7.0 Hz, 2 H), 2.34 (dt, J =
			11.4, 5.8 Hz, 1 H), 2.25 (ddd, J = 10.6, 7.5,
			5.2 Hz, 1 H), 2.21-2.11 (m, 2 H), 1.94-1.76
			(m, 4 H).
351	1-methoxy- 4- (isocyanato- methyl)ben- zene	27.2
			1-(4-methoxybenzyl)-3-(6-(pyridin-3-
			ylmethoxy)spiro[3.3]heptan-2-yl)urea.
			LRMS (APCI) m/z 382.20(M + H). 1H NMR
			(400 MHz, DMSO-d6) δ 8.58-8.43 (m, 2
			H), 7.72 (dt, J = 7.8, 2.0 Hz, 1 H), 7.37 (dd,
			J = 7.8, 4.8 Hz, 1 H), 7.14 (d, J = 8.6 Hz, 2
			H), 6.86 (d, J = 8.6 Hz, 2 H), 6.14-6.06 (m,
			2 H), 4.37 (s, 2 H), 4.09 (d, J = 5.8 Hz, 2
			H), 3.93 (h, J = 7.7, 7.1 Hz, 2 H), 3.72 (s, 3
			H), 2.34 (dt, J = 11.3, 6.0 Hz, 1 H), 2.29-
			2.21 (m, 1 H), 2.21-2.11 (m, 2 H), 1.93-
			1.74 (m, 4 H).

Example 25

Preparation of 1-(4-chlorobenzyl)-3-(6-((4-cyano-1H-pyrazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea (Compound 333)

1-(4-chlorobenzyl)-3-(6-((4-cyano-1H-pyrazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea. To a solution of 1-(4-chlorobenzyl)-3-(6-(hydroxymethyl)spiro[3.3]heptan-2-yl)urea (Intermediate 10.1, 120 mg, 0.389 mmol, 1.0 equiv) in CH₂Cl₂ (2 mL) was added Et₃N (118 mg, 1.17 mmol, 3.0 equiv) and MsCl (89 mg, 0.777 mmol, 2.0 equiv) sequentially. The mixture was stirred at 23° C. for 3 h before it was poured into a half-saturated NaHCO₃ solution. The aqueous phase was extracted by CH₂Cl₂ (5 mL×2) and the combined organic phase was washed by brine, dried (MgSO₄), filtered, and concentrated to yield the crude mesylate which was used directly without further purifications. Next, to a solution of so-obtained mesylate (up to 0.389 mmol) in DMF (1 mL) was added K₂CO₃ (107 mg, 0.777 mmol, 2.0 equiv) and 1H-pyrazole-4-carbonitrile (72 mg, 0.777 mmol, 2.0 equiv). The reaction was heated at 80° C. for 3 h. Upon completion, the reaction was directly subjected to preparative HPLC (H₂O (0.1% HCO₂H)/MeCN (0.1% HCO₂H) to yield 1-(4-chlorobenzyl)-3-(6-((4-cyano-1H-pyrazol-1-yl)methyl)spiro[3.3]heptan-2-yl)urea (61 mg, 40% over 2 steps) as a white solid. LRMS (APCI+) m/z 384.15 (M+H). ¹H NMR (400 MHz, DMSO-d₆) δ 8.55 (s, 1H), 8.04 (s, 1H), 7.36 (d, J=8.4 Hz, 2H), 7.24 (d, J=8.2 Hz, 2H), 6.25 (t, J=6.1 Hz, 1H), 6.17 (d, J=8.0 Hz, 1H), 4.15 (d, J=6.7 Hz, 4H), 3.90 (h, J=8.2 Hz, 1H), 2.60 (hept, J=7.7 Hz, 1H), 2.31 (ddd, J=10.7, 7.3, 5.1 Hz, 1H), 2.16 (ddd, J=12.1, 7.4, 5.2 Hz, 1H), 2.07 (ddd, J=11.3, 7.9, 3.5 Hz, 1H), 1.92 (ddd, J=11.5, 7.9, 3.4 Hz, 1H), 1.80 (dd, J=11.3, 8.2 Hz, 2H), 1.74 (dd, J=11.3, 8.4 Hz, 2H).

Compounds in the following table were prepared in a similar manner as Compound 333, using the intermediates and reagents as listed.

Compound
No.	Intermediate	Nucleophile	Structure, Name and Data
339	10.1	1,2,4-triazole
			1-(6-((1H-1,2,4-triazol-1-
			yl)methyl)spiro[3.3]heptan-2-yl)-3-(4-
			chlorobenzyl)urea. LRMS (APCI) m/z
			360.10 (M + H). 1H NMR (400 MHz,
			DMSO-d6) δ 8.49 (s, 1 H), 7.93 (s, 1 H),
			7.36 (d, J = 8.4 Hz, 2 H), 7.23 (d, J = 7.6
			Hz, 2 H), 6.26 (t, J = 6.1 Hz, 1 H), 6.18 (d,
			J = 8.0 Hz, 1 H), 4.15 (d, J = 6.7 Hz, 4 H),
			3.90 (h, J = 8.2 Hz, 1 H), 2.59 (p, J = 7.7
			Hz, 1 H), 2.31 (dt, J = 11.8, 6.2 Hz, 1 H),
			2.16 (dt, J = 12.1, 6.3 Hz, 1 H), 2.07 (td, J =
			9.4, 7.9, 3.2 Hz, 1 H), 1.92 (td, J = 9.6,
			7.7, 3.3 Hz, 1 H), 1.85-1.69 (m, 4 H).
352	10.1	Sodium benzenesulfi- nate
			1-(4-chlorobenzyl)-3-(6-
			((phenylsulfonyl)methyl)spiro[3.3]heptan-
			2-yl)urea. LRMS (APCI) m/z 433.10
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			7.87 (d, J = 7.9 Hz, 2 H), 7.75 (t, J = 7.3
			Hz, 1 H), 7.66 (t, J = 7.6 Hz, 2 H), 7.35 (d,
			J = 8.1 Hz, 2 H), 7.23 (d, J = 8.1 Hz, 2 H),
			6.24 (t, J = 6.1 Hz, 1 H), 6.13 (d, J = 8.1
			Hz, 1 H), 4.14 (d, J = 6.0 Hz, 2 H), 3.83 (q,
			J = 8.0 Hz, 1 H), 3.40 (d, J = 7.3 Hz, 2 H),
			2.43-2.24 (m, 3 H), 2.12-1.97 (m, 2 H),
			1.89-1.80 (m, 1 H), 1.69 (dq, J = 18.7, 9.8
			Hz, 4 H).
353	10.1	Sodium 3- pyridylsulfi- nate
			1-(4-chlorobenzyl)-3-(6-((pyridin-3-
			ylsulfonyl)methyl)spiro[3.3]heptan-2-
			yl)urea. LRMS (APCI) m/z 434.10
			(M + H). 1H NMR (400 MHz, DMSO-d6) δ
			9.01 (s, 1 H), 8.92 (d, J = 4.8 Hz, 1 H),
			8.27 (dt, J = 8.0, 1.9 Hz, 1 H), 7.70 (dd, J =
			8.1, 4.8 Hz, 1 H), 7.35 (d, J = 8.2 Hz, 2 H),
			7.22 (d, J = 8.1 Hz, 2 H), 6.25 (t, J = 6.1
			Hz, 1 H), 6.13 (d, J = 8.0 Hz, 1 H), 4.14 (d,
			J = 6.1 Hz, 2 H), 3.84 (h, J = 8.2 Hz, 1 H),
			3.53 (d, J = 7.2 Hz, 2 H), 2.41 (p, J = 7.9
			Hz, 1 H), 2.34-2.25 (m, 1 H), 2.12-1.99
			(m, 2 H), 1.86 (ddd, J = 11.9, 7.8, 4.4 Hz, 1
			H), 1.72 (dd, J = 19.9, 10.2 Hz, 2 H), 1.66
			(t, J = 11.1 Hz, 1H).

Biological Example 1

NMN Fluorescence Biochemical and NAD Cellular Assay

A. Human Recombinant Enzyme Assay

Compounds described herein were assayed for their ability to stimulate the synthesis of nicotinamide mononucleotide (NMN) by the enzyme NAMPT. The human recombinant enzyme assay measures the activation of the enzyme activity by compounds using recombinant enzyme and substrates in a buffered cell-free system. The assay conditions closely mimic cellular environments. Dose responses were measured using an assay to detect the formation of nicotinamide mono-nucleotide. All experiments were performed in the 384-well format. Generally, 0.5 μL of DMSO containing varying concentrations of the test compound was mixed with 10 μL of the enzyme reagent solution. Enzyme reactions were initiated with the addition of 10 μL of a solution containing the substrates. The final assay conditions were as follows: 6 nM human NAMPT, 2.5 mM ATP, 20 μM PRPP and 150 μM nicotinamide in 50 mM HEPES, pH 7.2, 1 mM DTT, 1 mM CHAPS 50 mM NaCl, 100 mM MgCl₂. Following an incubation of 60 min at ambient temperature, 10 μL of 20% acetophenone in DMSO was added, followed by 10 μL of 2 M KOH and 40 μL of formic acid. The plates were read for fluorescence (Excitation/Emission=355 nm/460 nm) using an EnVision plate reader after 40 mins of incubation at ambient temperature. The potency measurements for compounds, are quantified and represented as AC_1.4 (the concentration of compounds that generates 40% higher activity over basal) and EC₅₀ (concentration of the compound that gives half-maximal activation). Table A shows the AC_1.4 and EC₅₀ data and for the tested compounds.

TABLE A
	AC1.4	EC50
Compound	Human	Human
No.	(μM)	(μM)
1	0.1	0.8
2	1.0	25.9
3	17.5	41.4
4	9.9	28.5
5	14.5	48.6
6	4.5	26.8
7	5.1	26.3
8	5.4	5.1
9	3.4	47.0
10	5.8	50.7
11	11.5	N.D.
12	12.9	40.0
13	17.5	N.D.
14	2.7	35.3
15	10.4	17.7
16	0.1	0.3
17	17.6	50.5
18	18.9	60.2
19	0.1	1.8
20	0.2	4.7
21	8.0	45.0
22	0.1	1.1
23	0.1	1.4
24	8.1	29.1
25	5.0	27.4
26	2.0	16.7
27	4.1	21.5
28	13.9	42.5
29	3.2	26.7
30	10.2	37.9
31	3.2	40.1
32	10.5	N.D.
33	1.6	19.8
34	12.1	37.7
35	15.4	40.2
36	9.8	35.4
37	4.2	58.9
38	13.7	43.7
39	5.6	41.9
40	17.2	24.0
41	5.0	53.5
42	10.7	42.2
43	4.9	46.4
44	10.1	36.5
45	6.6	51.7
46	6.8	41.3
47	6.5	40.6
48	4.7	52.1
49	6.6	46.8
50	17.9	32.8
51	1.5	53.1
52	4.2	43.8
53	0.3	8.5
54	1.4	29.4
55	1.1	40.6
56	9.0	47.7
57	1.0	25.8
58	11.3	39.6
59	11.2	40.5
60	0.3	6.1
61	2.5	34.9
62	1.2	23.6
63	4.4	4.4
64	1.4	50.1
65	2.6	50.0
66	3.3	37.8
67	2.3	35.9
68	5.1	45.2
69	4.7	38.4
70	3.9	38.6
71	0.1	1.5
72	0.8	10.0
73	1.2	7.7
74	0.8	13.3
75	11.5	42.0
76	0.7	17.8
77	7.2	35.1
78	4.4	45.2
79	1.4	39.8
80	2.4	45.4
81	12.5	37.2
82	10.7	52.3
83	19.3	30.4
84	0.1	2.8
85	0.1	1.6
86	4.7	49.4
87	0.6	27.4
88	16.3	48.8
89	10.3	33.7
90	0.3	5.1
91	3.7	13.0
92	2.9	13.5
93	6.3	34.8
94	11.0	38.7
95	4.3	13.3
96	2.6	4.1
97	1.3	2.7
98	3.0	7.0
99	5.1	3.9
100	8.5	10.3
101	0.2	2.7
102	8.0	33.3
103	0.3	7.0
104	0.5	10.7
105	0.1	2.2
106	0.1	1.8
107	2.9	48.8
108	0.1	1.4
109	3.5	10.2
110	0.7	3.9
111	1.0	26.8
112	3.0	46.9
113	3.8	51.6
114	11.0	33.1
115	10.2	14.7
116	8.0	51.3
117	3.2	33.9
118	3.0	14.2
119	3.8	16.7
120	0.5	2.6
121	1.5	5.7
122	5.9	47.6
123	2.8	51.5
124	1.3	24.9
125	7.9	51.2
126	5.3	49.4
127	1.4	33.1
128	0.6	20.8
129	7.3	30.2
130	18.1	48.0
131	17.6	48.5
132	15.0	42.8
133	17.5	61.2
134	0.6	7.2
135	3.7	38.5
136	9.8	57.7
137	13.8	53.3
138	5.7	43.2
139	16.4	44.9
140	7.5	52.5
141	4.7	49.4
142	1.8	33.3
143	8.0	45.6
144	16.0	54.0
145	1.4	45.3
146	4.1	38.7
147	5.8	58.2
148	3.9	47.1
149	0.3	4.9
150	2.0	5.3
151	6.8	41.2
152	7.9	38.3
153	2.3	26.3
154	2.1	31.0
155	2.7	52.1
156	11.0	45.8
157	4.1	47.6
158	2.7	39.1
159	8.7	23.1
160	13.6	42.6
161	7.5	15.7
162	6.2	21.7
163	12.4	27.9
164	12.6	40.1
165	15.9	49.4
166	14.2	42.8
167	11.8	27.5
168	9.5	39.3
169	7.1	9.3
170	15.1	46.9
171	17.3	24.9
172	1.9	22.9
173	1.7	20.2
174	2.0	29.5
175	5.5	55.1
176	2.0	21.9
177	2.8	11.2
178	3.1	21.4
179	0.8	12.4
180	7.8	37.6
181	3.0	29.7
182	6.1	20.5
183	11.2	56.0
184	10.0	37.9
185	11.6	22.0
186	16.0	53.4
187	0.4	0.6
188	0.9	13.4
189	1.4	21.3
190	1.8	34.0
191	1.3	23.8
192	12.1	52.8
193	3.6	14.6
194	8.8	5.9
195	17.1	23.5
196	3.7	25.5
197	3.7	13.5
198	13.9	N.D.
199	10.6	42.2
200	17.1	18.2
201	6.7	22.2
202	0.9	2.2
203	8.2	34.3
204	13.6	26.8
205	10.0	23.6
206	2.2	4.3
207	13.7	6.6
208	9.6	11.8
209	10.6	38.5
210	1.9	49.9
211	0.5	27.8
212	7.2	6.0
213	6.8	6.8
214	10.5	36.7
215	3.6	30.8
216	4.9	20.9
217	19.2	20.1
218	13.2	22.5
219	2.9	5.2
220	3.6	4.7
221	1.1	4.6
222	0.2	28.6
223	0.2	38.5
224	0.6	47.5
225	2.0	50.8
226	2.9	31.4
227	2.0	33.8
228	1.9	39.2
229	0.1	1.2
230	1.8	30.9
231	0.5	7.8
232	3.6	37.8
233	0.9	1.0
234	3.7	8.6
235	4.1	7.5
236	3.6	5.7
237	2.4	2.6
238	3.4	20.3
239	2.1	22.5
240	0.9	3.0
241	2.7	5.7
242	3.6	0.8
243	1.5	4.2
244	3.4	7.3
245	3.1	4.9
246	2.1	4.2
247	2.8	7.9
248	5.0	6.6
249	1.0	2.7
250	1.8	7.7
251	2.6	6.1
252	2.8	9.1
253	3.2	5.5
254	1.5	2.3
255	2.5	6.5
256	1.0	2.0
257	2.7	17.9
258	3.8	23.1
259	8.6	59.4
260	2.0	17.5
261	2.8	42.9
262	0.6	4.9
263	1.4	10.2
264	1.0	6.7
265	0.8	1.6
266	0.5	1.8
267	2.0	7.9
268	0.3	0.5
269	0.7	5.1
270	1.1	3.9
271	0.9	3.7
272	0.9	2.6
273	0.9	0.3
274	1.9	0.3
275	1.9	11.4
276	1.5	9.5
277	3.2	6.9
278	1.8	7.1
279	1.8	11.8
280	0.7	2.6
281	1.3	3.9
282	0.1	3.9
283	8.6	32.8
284	2.8	4.2
285	3.5	9.4
286	0.2	2.0
287	0.1	4.4
288	0.3	3.7
289	1.1	7.7
290	1.3	6.2
291	1.9	4.6
292	0.5	2.0
293	0.1	1.5
294	1.0	10.1
295	1.2	8.4
296	0.8	2.0
297	0.1	0.2
298	1.1	2.9
299	1.0	3.8
300	1.4	6.5
301	2.7	26.3
302	2.0	7.9
303	2.6	15.6
304	1.7	10.6
305	0.2	0.4
306	0.4	1.2
307	1.9	7.3
308	2.2	5.0
309	2.1	6.5
310	0.8	4.1
311	1.2	3.4
312	1.5	5.4
313	0.7	1.4
314	0.5	0.7
315	0.9	2.0
316	1.4	6.4
317	4.2	25.1
318	3.9	8.8
319	0.8	0.8
320	0.1	1.4
321	0.1	2.1
322	0.1	2.3
323	0.2	1.6
324	0.2	1.9
325	2.4	30.6
326	4.5	2.9
327	4.1	17.4
328	1.2	4.3
329	62.5	>62.5
330	0.1	3.9
331	2.2	1.3
332	6.2	28.5
333	1.8	4.4
334	2.3	2.7
335	1.1	2.2
336	0.7	2.1
337	1.0	26.1
338	6.4	10.3
339	4.6	6.5
340	3.7	5.6
341	3.9	2.0
342	33.1	56.1
343	3.0	5.6
344	3.1	34.9
345	1.6	0.6
346	62.5	>62.5
347	2.2	2.4
348	5.0	5.9
349	6.9	40.3
350	1.7	6.1
351	4.0	38.7
352	6.0	8.0
353	5.3	16.9
354	4.2	10.8
N.D. = Not Determined

B. Cellular NAD+ Modulation Assay.

The compounds described herein were also assayed for their ability to stimulate the endogenous NAMPT in a native cellular environment in the cellular NAD+ modulation assay, which measures the ability of the compound to modulate cellular NAD levels. Increased levels of NAD are expected by compounds that permeate the cells and activate the catalytic activity of the endogenous NAMPT.

Neuroblastoma SH-SY5Y cells were grown in 1:1 mixture of Eagle's Minimum Essential Medium and F12 Medium, along with 10% fetal bovine serum, in a humidified incubator with an atmosphere of 95% air and 5% CO₂ at 37° C. The assays were initiated by plating 20 μL of SH-SY5Y cells in culture medium with 0.1% fetal bovine serum, at a density of 5000 cells per well to a 384-well Corning™ BioCoat™ Poly-D-Lysine Multiwell Plates. The plates were incubated in the 37° C. incubators for a period of 5 hours. Compounds in DMSO were added to the plates in a volume of 120 nL using the Labcyte Echo Liquid Handlers. 5 μL of a 1.5 uM Doxorubicin solution in assay medium is added to each well. The plates are then incubated for 40 hours. 30 μL of a readout-solution containing 0.2 U/mL Diaphorase enzyme, 40 uM resazurin, 10 uM FMN, 0.8 U/mL Alcohol dehydrogenase, 3% ethanol, 0.4 mg/mL bovine serum albumin, 0.2% Triton X-100 in 100 mM Tris-HCl, 30 mM EDTA, pH 8.4. The plates were read for fluorescence (Excitation/Emission=540 nm/590 nm) using an EnVision plate reader after 60 mins of incubation at ambient temperature. Table B shows the AC_0.3 and EC₅₀ data for the tested compounds.

TABLE B
Compound	AC0.3	EC50
No.	(μM)	(μM)
7	2.4	4.7
14	>20.1	20.1
16	0.1	0.1
19	1.6	1.3
20	0.4	13.9
22	0.4	0.1
23	0.3	0.3
27	1.4	5.8
29	3.0	2.2
33	7.9	8.4
71	0.3	0.9
72	2.5	10.8
73	0.8	0.8
74	0.3	0.5
76	5.9	4.7
79	5.8	5.8
84	5.3	12.7
85	0.9	0.8
87	3.4	2.4
90	0.9	0.8
110	0.5	0.3
120	0.2	0.3
121	0.6	1.2
134	8.0	12.7
138	9.1	10.1
140	8.2	6.3
145	1.1	3.1
149	0.6	1.1
161	0.3	0.8
162	0.7	1.0
164	11.6	12.9
187	0.2	0.2
196	1.0	3.3
199	2.0	N.D.
202	0.5	0.6
203	8.9	10.0
206	0.2	0.5
210	9.7	9.0
211	>20.1	N.D.
212	0.3	0.1
214	>20.1	N.D.
229	0.1	0.2
249	0.5	0.9
256	0.3	0.3
268	0.1	0.1
287	0.3	1.0
288	0.3	0.8
293	0.3	0.3
322	0.2	0.3
329	0.1	0.1
330	0.5	8.1
346	0.1	0.1
N.D. = Not Determined

All publications, patent applications, patents, and other references mentioned herein are expressly incorporated by reference in their entireties, to the same extent as if each were incorporated by reference individually.

It is to be understood that, while the disclosure provided herein has been described in conjunction with the above embodiments, the foregoing description and examples are intended to illustrate and not limit the scope of the disclosure. Other aspects, advantages and modifications within the scope of the disclosure will be apparent to those skilled in the art to which the disclosure pertains.

Claims

1. A compound of Formula (II):

2. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

3. The compound of claim 1 or claim 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 1 and q1 is 1.

4. The compound of claim 1 or claim 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 2 and q1 is 1.

5. The compound of claim 1 or claim 2, or a pharmaceutically acceptable salt thereof, wherein p1 is 2 and q1 is 2.

6. The compound of any one of claims 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 1 and q2 is 1.

7. The compound of any one of claims 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 0 and q2 is 1.

8. The compound of any one of claims 1-5, or a pharmaceutically acceptable salt thereof, wherein p2 is 1 and q2 is 2.

9. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is unsubstituted C1-C6 alkyl.

10. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C6-C14 aryl.

11. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is 5- to 18-membered heteroaryl optionally substituted with one or more Ra substituents, wherein Ra is C1-C6 alkyl, C6-C14 aryl, or 5- to 18-membered heteroaryl, wherein the 5- to 18-membered heteroaryl of Ra is optionally substituted with one or more C1-C6 alkyl substituents.

12. The compound of claim 11, or a pharmaceutically acceptable salt thereof, wherein R3 is pyridyl, pyrimidyl, 1,3,4-oxadiazolyl, oxazolyl, or benzo[d]oxazolyl optionally substituted with one or more Ra substituents.

13. The compound of claim 11 or claim 12, or a pharmaceutically acceptable salt thereof, wherein R3 is

14. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —NR3aR3b, wherein R3a and R3b are each independently selected from the group consisting of hydrogen, C6-C14 aryl, 5- to 18-membered heteroaryl, —(C1-C6 alkylene)-(C6-C14 aryl), and —(C1-C6 alkylene)-(5- to 18-membered heteroaryl).

15. The compound of claim 14, or a pharmaceutically acceptable salt thereof, wherein R3 is

16. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is OR3c, wherein R3c is C6-C14 aryl, 5- to 18-membered heteroaryl, or —(C1-C6 alkylene)-(5- to 18-membered heteroaryl).

17. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —C(O)R3d.

18. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is —NR3fR3g and R3f and R3g are each independently selected from the group consisting of: (a) hydrogen,(b) C1-C6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of —OH, C6-C14 aryl, and 5- to 18-membered heteroaryl, wherein the C6-C14 aryl and 5- to 18-membered heteroaryl groups are each independently unsubstituted or substituted with one or more substituents independently selected from the group consisting of halo, C1-C6 alkyl, hydroxyl, C1-C6alkoxy, C1-C6 haloalkoxy, and CN,(c) C6-C14 aryl,(d) 3- to 18-membered heterocycloalkyl,(e) 5- to 18-membered heteroaryl optionally substituted with methyl or CN,(f) C3-C10 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxyl, C1-C6 alkyl optionally substituted with hydroxyl, C6-C14 aryl, and 5- to 18-membered heteroaryl; and(g) C3-C10 cycloalkenyl optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxyl, C1-C6 alkyl optionally substituted with hydroxyl, C6-C14 aryl, and 5- to 18-membered heteroaryl.

19. The compound of claim 17 or claim 18, or a pharmaceutically acceptable salt thereof, wherein R3 is

20. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is C3-C8 cycloalkyl.

21. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is C3-C8 cycloalkyl substituted with C6-C14 aryl, wherein the C6-C14 aryl is optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-C6 alkyl, C1-C6 haloalkyl, and C1-C6 alkoxy.

22. The compound of claim 20 or claim 21, or a pharmaceutically acceptable salt thereof, wherein R3 is

23. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is C3-C8 cycloalkenyl.

24. The compound of claim 23, or a pharmaceutically acceptable salt thereof, wherein R3 is

25. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is C6-C14 aryl optionally substituted with one or more substituents independently selected from the group consisting of hydroxyl, halo, cyano, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, —(C1-C6 alkylene)-OH, —C(O)O(C1-C6 alkyl), —NR3e1R3e2, —S(O)2(C1-C6 alkyl), 5- to 18-membered heteroaryl, and 3- to 18-membered heterocycloalkyl optionally substituted with oxo, wherein R30 1 and R3e2 are each independently H or C1-C6 alkyl.

26. The compound of claim 25, or a pharmaceutically acceptable salt thereof, wherein R3 is

27. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is —(C1-C6 alkylene)-(C6-C14 aryl) optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-C6 alkyl, C1-C6 haloalkyl, and C1-C6 alkoxy.

28. The compound of claim 27, or a pharmaceutically acceptable salt thereof, wherein R3 is

29. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is 3- to 18-membered heterocycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of: (a) C1-C6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of hydroxyl, halo, C3-C10 cycloalkyl, and 5- to 18-membered heteroaryl optionally substituted with one or more C1-C6 alkyl substituents,(b) C6-C14 aryl,(c) 3- to 18-membered heterocycloalkyl,(d) —C(O)O(C1-C6 alkyl),(e) —C(O)(C6-C14 aryl),(f) halo,(g) C1-C6 alkoxy optionally substituted with one or more halo substituents, and(h) oxo.

30. The compound of claim 29, or a pharmaceutically acceptable salt thereof, wherein R3 is

31. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R3d is 5- to 18-membered heteroaryl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl, hydroxyl, oxo, and 3- to 18-membered heterocycloalkyl.

32. The compound of claim 31, or a pharmaceutically acceptable salt thereof, wherein R3 is

33. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl substituted with C(O)NR3hR3i, wherein R3h and R3i are each independently selected from C1-C6 alkyl and —(C1-C6 alkylene)-(C6-C14 aryl).

34. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein R3 is

35. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl substituted with 3- to 18-membered heterocycloalkyl, wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more substituents independently selected from halo, oxo, C1-C6 alkyl, C6-C14 aryl, and 5- to 18-membered heteroaryl.

36. The compound of claim 35, or a pharmaceutically acceptable salt thereof, wherein R3 is

37. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl, wherein the C1-C6 alkyl of R3 is (i) substituted with 5- to 18-membered heteroaryl, wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more C1-C6 alkyl, C6-C14 aryl, or cyano, and (ii) optionally substituted with one or more —OH.

38. The compound of claim 37, or a pharmaceutically acceptable salt thereof, wherein R3 is

39. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —C(O)OR3j, wherein R3j is hydrogen or C1-C6 alkyl.

40. The compound of claim 39, or a pharmaceutically acceptable salt thereof, wherein R3 is

41. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —NHC(O)R3k.

42. The compound of claim 41, or a pharmaceutically acceptable salt thereof, wherein R3k is C6-C14 aryl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl, cyano, —NR3k1R3k2, hydroxy, alkoxy, and S(O)-2(alkyl), wherein R3k1 and R3k2 are each independently hydrogen or C1-C6 alkyl.

43. The compound of claim 41 or claim 42, or a pharmaceutically acceptable salt thereof, wherein R3 is

44. The compound of claim 41, or a pharmaceutically acceptable salt thereof, wherein R3k is —(C1-C6 alkylene)-(C6-C14 aryl), optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl, cyano, —NR3k1R32, hydroxy, alkoxy, and S(O)2(alkyl), wherein R3k1 and R3k2 are each independently hydrogen or C1-C6 alkyl.

45. The compound of claim 41 or claim 44, or a pharmaceutically acceptable salt thereof, wherein R3 is

46. The compound of claim 41, or a pharmaceutically acceptable salt thereof, wherein R3k is 5- to 18-membered heteroaryl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl, cyano, —NR3k1R32, hydroxy, alkoxy, and S(O)2(alkyl), wherein R3k1 and R3k2 are each independently hydrogen or C1-C6 alkyl.

47. The compound of claim 41 or claim 46, or a pharmaceutically acceptable salt thereof, wherein R3 is

48. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —NHC(O)OR31, wherein R31 is hydrogen or C1-C6 alkyl.

49. The compound of claim 48, or a pharmaceutically acceptable salt thereof, wherein R3 is

50. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —NHSO2R3m, wherein R3m is 5- to 18-membered heteroaryl, C6-C14 aryl, or —(C1-C6 alkylene)-(C6-C14 aryl), wherein the 5- to 18-membered heteroaryl, the C6-C14 aryl, and the —(C1-C6 alkylene)-(C6-C14 aryl) are each optionally substituted with one or more substituents independently selected from halo and C1-C6 alkoxy.

51. The compound of claim 50, or a pharmaceutically acceptable salt thereof, wherein R3 is

52. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is —SO2R3n and R3n is C1-C6 alkyl, C3-C10 cycloalkyl, C6-C14 aryl, or —(C1-C6 alkylene)-(C6-C14 aryl), wherein the C3-C10 cycloalkyl, the C6-C14 aryl, and the —(C1-C6 alkylene)-(C6-C14 aryl) of R3n are each independently optionally substituted with one or more substituents independently selected from halo and —C(O)O(C1-C6 alkyl).

53. The compound of claim 52, or a pharmaceutically acceptable salt thereof, wherein R3 is

54. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl substituted with one or more —N(R3P)—C(O)R3q, wherein R3p is H or C1-C6 alkyl, and R3q is (i) C3-C8 cycloalkyl, (ii) 3- to 18-membered heterocycloalkyl optionally substituted with one or more independently selected oxo substituents, or (iii) 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C1-C6alkyl substituents.

55. The compound of claim 54, or a pharmaceutically acceptable salt thereof, wherein R3 is

56. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl substituted with one or more —S(O)2—R3r, wherein R3r is C6-C14 aryl or 5- to 18-membered heteroaryl.

57. The compound of claim 56, or a pharmaceutically acceptable salt thereof, wherein R3 is

58. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl substituted with one or more —C(O)—R3s, wherein R3s is 3- to 18-membered heterocycloalkyl optionally substituted with one or more independently selected C1-C6 alkyl substituents, wherein the C1-C6 alkyl is independently optionally substituted with one or more —OH.

59. The compound of claim 58, or a pharmaceutically acceptable salt thereof, wherein R3 is

60. The compound of any one of claims 1-8, or a pharmaceutically acceptable salt thereof, wherein R3 is C1-C6 alkyl, wherein the C1-C6 alkyl of R3 is (i) substituted with one or more independently selected C6-C14 aryl substituents, wherein the C6-C14 aryl is optionally substituted with one or more independently selected C1-C6 alkyl substituents, and (ii) optionally substituted with one or more —OH.

61. The compound of claim 60, or a pharmaceutically acceptable salt thereof, wherein R3 is

62. The compound of any one of claims 1-61, or a pharmaceutically acceptable salt thereof, wherein G1 is CH.

63. The compound of any one of claims 1-61, or a pharmaceutically acceptable salt thereof, wherein G1 is N.

64. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

65. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

66. The compound of claim 65, or a pharmaceutically acceptable salt thereof, wherein r is 1.

67. The compound of claim 65, or a pharmaceutically acceptable salt thereof, wherein r is 2.

68. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

69. The compound of claim 68, or a pharmaceutically acceptable salt thereof, wherein R4 is phenyl.

70. The compound of claim 68, or a pharmaceutically acceptable salt thereof, wherein R4 is —C(O)NH—CH2-phenyl.

71. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

72. The compound of claim 71, or a pharmaceutically acceptable salt thereof, wherein R5a is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C1-C6 alkyl).

73. The compound of claim 71 or claim 72, or a pharmaceutically acceptable salt thereof, wherein R5b is selected from the group consisting of hydrogen, methyl, and —NHC(O)O(C1-C6 alkyl).

74. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

75. The compound of claim 74, or a pharmaceutically acceptable salt thereof, wherein R6 is selected from the group consisting of: (a) —C(O)OC(CH3)3;(b) —NHC(O)O(C1-C6 alkyl);(c) —C(O)-(phenyl), wherein the phenyl is optionally substituted with one or more substituents independently selected from C1-C6 alkyl, C1-C6 haloalkyl, and 5- to 18-membered heteroaryl;(d) —C(O)—(C1-C6 alkylene)-(phenyl), wherein the phenyl is optionally substituted with one or more independently selected C1-C6 alkyl substituents;(e) —C(O)-(3- to 18-membered heterocycloalkyl), wherein the 3- to 18-membered heterocycloalkyl is optionally substituted with one or more independently selected oxo or C1-C6alkyl substituents;(f) —C(O)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C1-C6 alkyl substituents;(g) —C(O)—(C1-C6 alkylene)-(5- to 18-membered heteroaryl), wherein the 5- to 18-membered heteroaryl is optionally substituted with one or more independently selected C1-C6 alkyl substituents; and(h) 5- to 18-membered heteroaryl.

76. The compound of claim 75, or a pharmaceutically acceptable salt thereof, wherein R6 is —C(O)-(phenyl), wherein the phenyl is optionally substituted with one or more C1-C6 alkyl, C1-C6 haloalkyl, or 5- to 18-membered heteroaryl.

77. The compound of claim 75 or claim 76, or a pharmaceutically acceptable salt thereof, wherein R6 is

78. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is —C(O)—N(Rq)—(Rs), wherein Rq is H or C1-C6 alkyl, and Rs is (a) C3-C8 cycloalkyl;(b) C6-C14 aryl optionally substituted with one or more substituents independently selected from halo, C1-C6 alkyl, and C6-C14 aryl;(c) 5- to 18-membered heteroaryl optionally substituted with one or more C1-C6 alkyl; or(d) —(C1-C6 alkylene)-(C6-C14 aryl), wherein the C6-C14 aryl of the —(C1-C6 alkylene)-(C6-C14 aryl) is optionally substituted with one or more C1-C6 alkyl.

79. The compound of claim 78, or a pharmaceutically acceptable salt thereof, wherein Y1 is

80. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is —C(O)—Rb, wherein Rb is 3- to 18-membered heterocycloalkyl optionally substituted with one or more C1-C6 alkyl, wherein the C1-C6 alkyl is optionally substituted with one or more —OH.

81. The compound of claim 80, or a pharmaceutically acceptable salt thereof, wherein Y1 is

82. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is —N(Rt)—C(O)Ru, wherein Rt is H or C1-C6 alkyl, and Ru is (a) C6-C14 aryl optionally substituted with one or more independently selected C1-C6alkyl or halo substituents;(b) 5- to 18-membered heteroaryl optionally substituted with one or more independently selected C1-C6 alkyl substituents; or(c) —(C1-C6 alkylene)-(5- to 18-membered heteroaryl).

83. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

84. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y1 is

85. The compound of any one of claims 1-63, 65, 66, and 68-77, or a pharmaceutically acceptable salt thereof, wherein n is 0.

86. The compound of any one of claims 1-63, 65, 66, and 68-77, or a pharmaceutically acceptable salt thereof, wherein n is 1.

87. The compound of any one of claims 1-63 and 65-77, or a pharmaceutically acceptable salt thereof, wherein n is 2.

88. The compound of any one of claims 1-63 and 65-77, or a pharmaceutically acceptable salt thereof, wherein n is 3.

89. The compound of any one of claims 1-84, or a pharmaceutically acceptable salt thereof, wherein n is 4.

90. The compound of any one of claims 1-84, or a pharmaceutically acceptable salt thereof, wherein n is 5.

91. The compound of any one of claims 1-77, or a pharmaceutically acceptable salt thereof, wherein n is 6.

92. The compound of any one of claims 1-79 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

93. The compound of any one of claims 1-79 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

94. The compound of any one of claims 1-67 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

95. The compound of any one of claims 1-77 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is selected from the group consisting of and

96. The compound of any one of claims 1-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

97. The compound of any one of claims 1-77 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

98. The compound of any one of claims 1-77 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

99. The compound of any one of claims 1-77 and 85-91, or a pharmaceutically acceptable salt thereof, wherein R1 is

100. A compound selected from the group consisting of compounds of Table 1, or a pharmaceutically acceptable salt thereof.

101. A pharmaceutical composition comprising a compound according to any one of claims 1-100, or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.

102. A method of treating a disease or condition mediated by NAMPT activity in a subject in need thereof, comprising administering to the subject a compound of any one of claims 1-100, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of claim 101.

103. The method of claim 102, wherein the disease or condition is selected from the group consisting of cancer, a hyperproliferative disease or condition, an inflammatory disease or condition, a metabolic disorder, a cardiac disease or condition, chemotherapy induced tissue damage, a renal disease, a metabolic disease, a neurological disease or injury, a neurodegenerative disorder or disease, diseases caused by impaired stem cell function, diseases caused by DNA damage, primary mitochondrial disorders, or a muscle disease or muscle wasting disorder.

104. The method of claim 102, wherein the disease or condition is selected from the group consisting of obesity, atherosclerosis, insulin resistance, type 2 diabetes, cardiovascular disease, Alzheimer's disease, Huntington's disease, Parkinson's disease, amyotrophic lateral sclerosis, depression, Down syndrome, neonatal nerve injury, aging, axonal degeneration, carpal tunnel syndrome, Guillain-Barre syndrome, nerve damage, polio (poliomyelitis), and spinal cord injury.