WO2004058736A1 - Ccr8 inhibitors - Google Patents

Ccr8 inhibitors Download PDF

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Publication number
WO2004058736A1
WO2004058736A1 PCT/US2003/041199 US0341199W WO2004058736A1 WO 2004058736 A1 WO2004058736 A1 WO 2004058736A1 US 0341199 W US0341199 W US 0341199W WO 2004058736 A1 WO2004058736 A1 WO 2004058736A1
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WIPO (PCT)
Prior art keywords
substituted
group
unsubstituted
aromatic
methyl
Prior art date
Application number
PCT/US2003/041199
Other languages
French (fr)
Inventor
Mingshi Dai
Tracy J. Jenkins
Bing Guan
Shomir Ghosh
Charles Minor
Original Assignee
Millennium Pharmaceuticals, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Millennium Pharmaceuticals, Inc. filed Critical Millennium Pharmaceuticals, Inc.
Priority to EP03800155A priority Critical patent/EP1581511A1/en
Priority to AU2003299883A priority patent/AU2003299883A1/en
Publication of WO2004058736A1 publication Critical patent/WO2004058736A1/en

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    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
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    • A61P13/00—Drugs for disorders of the urinary system
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
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    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
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    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
    • C07D211/28—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms to which a second hetero atom is attached
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

Definitions

  • Chemoattractant cytokines or chemokines are a family of proinflammatory mediators that promote recruitment and activation of multiple lineages of leukocytes and lymphocytes. They can be released by many kinds of tissue cells after activation. Continuous release of chemokines at sites of inflammation mediates the ongoing migration of effector cells in chronic inflammation (Baggiolini, et. al, Nature 15:365 (1994)). Indeed, chemokines have been implicated in a wide range of human acute and chronic inflammatory diseases including, but not limited to, respiratory diseases such as asthma, inflammatory bowel disease, allergic disorders and certain autoimmune diseases such as rheumatoid arthritis.
  • Chemokines exert their biological activity by binding to specific G-protein receptors, which then transduce signals important for the development and trafficking of specific leukocyte subsets (Baggiolini, et. al, Nature 15:365 (1994)).
  • a number of chemokine receptors have been characterized and each are differentially expressed among leukocyte populations.
  • each chemokine binds specifically to a single receptor or to a small group of receptors.
  • the recruitment and activation of specific classes of leukocytes or lymphocytes can be modulated by agents which selectively act at one chemokine receptor and/or block the activity of a specific chemokine.
  • CCR8 is a chemokine receptor (see WO 99/065561) whose expression is primarily restricted to Th2 cells (Zingoni et al, J. Immunol. 161:541 (1998) and D'Ambrosio et al, J. Immunol. 161:5111 (1998)).
  • 1-309 is a ligand for CCR8 and has shown to be chemotactic for the cells in vitro (D'Ambrosio et al, J. Immunol 161:5111 (1998). CCR8 is also involved in eosinophil recruitment (see WO 99/065561). Thus, antagonists for CCR8 are expected to be useful in treating disorders mediated by Th2 and eosinophil cells, e.g., asthma.
  • 1,4-naphthylsulfonamides also referred to herein as "1,4- naphthylene sulfonamides"
  • 1,4- naphthylene sulfonamides are effective inhibitors of CCR8 activity.
  • naphthylsulfonamides shown in the Tables at the end of the Experimental Section inhibit CCR8 activity with a Kj less than 1 ⁇ M.
  • novel CCR8 inhibitors, pharmaceutical compositions comprising these inhibitors and methods of treating inflammatory disorders with these inhibitors are disclosed herein.
  • One embodiment of the present invention is a compound (a CCR8 inhibitor) represented by Structural Formula (I):
  • X is a covalent bond, O or NR .
  • Xi is a covalent bond; in another preferred embodiment, Xi is CH 2 .
  • R a and R b are independently -H or a C1-C3 alkyl.
  • R 1 is a substituted or unsubstituted aromatic group or a substituted or unsubstituted non-aromatic ring.
  • X is NR 5
  • -NR 5 (CH 2 ) m R 1 taken together, is optionally a substituted or unsubstituted non-aromatic heterocyclic group.
  • R 2 is -H or a C1-C3 alkyl group.
  • R 3 is -H and R 4 is a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group, a substituted or unsubstituted non-aromatic ring or a substituted or substituted non-aromatic bridged bicyclic group (preferably, a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group, a substituted or unsubstituted non-aromatic ring, more preferably, a substituted or unsubstituted aromatic group, or a substituted or unsubstituted non-aromatic ring) or, R 3 and R 4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group.
  • R 5 is -H, or a C1-C3 alkyl group.
  • Rings A and B are independently substituted or unsubstituted.
  • Ring B is a phenyl ring or a five or six membered carbocyclic carbocyclic non- aromatic ring fused to Ring A.
  • Ring B is an optionally substituted phenyl or optionally substituted six membered non-aromatic carbocyclic ring (e.g., cyclohexyl or cyclohexenyl) fused to Ring A.
  • m is 0, 1, 2 or 3.
  • n is 1 or 2.
  • Another embodiment of the present invention method is a method of treating a subject with a CCR8 mediated condition or disease, e.g., a subject with asthma.
  • the method comprises the step of administering to the subject an effective amount of a CCR8 inhibitor disclosed herein.
  • compositions comprising a pharmaceutically acceptable carrier or diluent and a CCR8 inhibitor disclosed herein.
  • the pharmaceutical compositions can be used in therapy, for example, to treat a subject with a CCR8 mediated condition or disease, for example, a subject with asthma.
  • Yet another embodiment of the present invention is the use of one of the disclosed CCR8 inhibitors for the manufacture of a medicament for treating a subject with a CCR8 mediated condition or disease.
  • the medicament comprises an effective amount of the CCR8 inhibitor.
  • the disclosed compounds are effective inhibitors of CCR8 and, as such, are expected to be useful in the treatment and prevention of diseases mediated by CCR8, particularly asthma.
  • Other diseases for which the disclosed CCR8 inhibitors are expected to be effective include, but not limited to, inflammatory diseases such as atopic dermatitis, allergic rhinitis, systemic anaphylaxis or hypersensitivity responses, drug allergies (e.g., to penicillin, cephalosporins), insect sting allergies and inflammatory dermatoses such as dermatitis, eczema, allergic contact dermatitis, urticaria, atherosclerosis, restenosis and myositis (including polymyositis, dermatomyositis).
  • the present invention is directed to inhibitors of the chemokine receptor commonly referred to as "CCR8".
  • CCR8 is expressed on monocytes and Th2 lymphocytes and in the brain, spleen and thymus. It is the receptor for the chemokine I- 309, which is chemotactic for Th2 cells.
  • 1-309 has also shown to be involved in esinophil recruitment.
  • the disclosed compounds can be used to inhibit CCR8 activity; to inhibit 1-309 activity and to inhibit or treat (therapeutically or prophylactically) conditions mediated by CCR8 and/or 1-309, including inflammatory disorders and allergic conditions.
  • the disclosed compounds can also be advantageously used to inhibit conditions mediated by esinophils and by monocytes, T lymphocytes and other immune system cells which express CCR8, including inflammatory disorders and allergic conditions mediated by these cells.
  • R 10 and R 12 are provided below in the section describing suitable aromatic and aliphatic group substituents.
  • the compound is characterized by features (1); (2); (3); (4); (5); (6); (7); (8); (1) and (4); (1), (2) and (4); (1), (3) and (4); (1), (4) and (5); (1), (4), and (6); (1), (4) and (7); (1), (4) and (8); (1), (4), (7) and (8); (1), (2), (4), (7) and (8); (1), (3), (4), (7) and (8); (1), (4), (5), (7) and (8); (1), (4), (6), (7) and (8); (1), (2), (3), (4), (5), (7) and (8); (1), (2), (4), (5), (6), (7) and (8); and (1), (3), (4), (5), (6), (7) and (8).
  • the compound represented by Structural Formula (I) is characterized by all
  • the CCR8 inhibitor is represented by Structural Formula (TT):
  • the CCR8 inhibitor is represented by Structural Formula (ITI):
  • the CCR8 inhibitor is represented by Structural Formula (IV):
  • the CCR8 inhibitor is represented by Structural
  • the CCR8 inhibitor is represented by Structural Formula (VI):
  • the CCR8 inhibitor is represented by Structural Formula (VH):
  • the CCR8 inhibitor is represented by Structural Formula (Vm):
  • the CCR8 inhibitor is represented by Structural Formula (DC):
  • the CCR8 inhibitor is represented by Structural Formula (X):
  • R 1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more groups, for example, the substituent groups represented by R 10 ;
  • R 3 is -H and
  • R 4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups, for example the substituent groups represented by R 12 or R 3 and R 4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group;
  • m is 0 or 1; and Rings A and B are optionally and independently substituted at any one or more substitutable ring carbons.
  • R 10 and R 12 and exemplary substituents for Rings A and B are provided hereinbelow in the section describing aromatic group and non- aromatic ring substituents.
  • Preferred substituents for Rings A and B include alkyl, haloalkyl, alkoxy, haloalkoxy, hydroxy, halogen, cyano and nitro.
  • Rings A and B are unsubstituted.
  • One preferred value for R 4 in Structural Formulas (I)-(X) is a substituted or unsubstituted non-aromatic ring.
  • Suitable substituents for a non-aromatic ring represented by R 4 are provided hereinbelow in section describing substituents for a substitutable carbon on a non-aromatic ring and in the section describing substituents for the nitrogen atom of a non-aromatic heterocyclic group.
  • R 4 in Structural Formulas (I)-(X) is a non-aromatic ring, preferred values include a piperidinyl group, an N-substituted piperidinyl group, or a cyclohexyl group.
  • Suitable substituents for the nitrogen atom in a piperidinyl group represented by R 4 are provided hereinbelow in the section describing substituents on the nitrogen atom of a non-aromatic heterocyclic group.
  • Preferred substituents for the nitrogen atom in a piperidinyl group represented by R 4 include R 15 , -C(0)R 15 , -C(0)OR 15 , and -C(0)- ⁇ HR 15 .
  • Other preferred substituents for the nitrogen atom in a piperidinyl group represented by R 4 include -C(0)-N(R 15 ) 2 or -C(0)CH[N(R 16 ) 2 ]R 17 .
  • R 15 is -H, a non-aromatic ring, or a substituted or unsubstituted aliphatic group or a substituted or unsubstituted C7-C9 aralkyl group. Typically, however, -C(0)OR ls is not -COOH. R 15 can also be a substituted or unsubstituted non-aromatic ring. In addition, N(R 15 ) 2 taken together can be a substituted or unsubstituted five or six membered non-aromatic nitrogen-containing heterocyclic group.
  • Preferred substituents for a substitutable carbon of the non-aromatic ring represented by R 15 or the non-aromatic heterocyclic group represented by N(R 15 ) 2 included methyl, ethyl hydroxyethyl and iso- propyl; suitable substituents for a substitutable nitrogen of these groups include alkyl, alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl and dialkylaminocarbonyl.
  • R 16 is -H or an alkyl group.
  • R 17 is -H; a C1-C6 alkyl group optionally substituted with -OH, -NH 2 , phenyl or phenyl substituted with -OH; indolyl; imidazolyl; or phenyl optionally substituted with -OH.
  • R 4 in Structural Formulas (I)-(X) is a phenyl group, a substituted phenyl group, a benzyl group or a substituted benzyl group.
  • Suitable substituents for phenyl and benzyl groups represented by R 4 are provided hereinbelow in the section describing suitable aromatic group substituents.
  • Preferred substituents are electron donating groups such as methoxy, ethoxy, iso-propoxy, methyl, ethyl, propyl, NH 2 , NHCH 3 , N(CH 3 ) 2 , NHCH 2 CH 3 , N(CH 2 CH 3 ) 2 , N(CH 3 )(CH 2 CH 3 ), NH(CH 2 CH 2 CH 3 ), N(CH 2 CH 2 CH 3 ) 2 , N(CH 3 )(CH 2 CH 2 CH 3 ) or N(CH 2 CH 3 )(CH 2 CH 2 CH 3 ).
  • -NR 3 R 4 in Structural Formulas (I)-(X), taken together is a substituted or unsubstituted rion-aromatic heterocyclic group.
  • Suitable substituents for a non-aromatic heterocyclic group represented by -NR 3 R 4 are provided hereinbelow in section describing suitable substituents for a substitutable carbon of a non- aromatic group and in the section describing suitable substituents for the nitrogen atom of a non-aromatic heterocyclic group.
  • R 1 is preferably a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or a unsubstituted -CH 2 -(pyridyl) group, a substituted or a unsubstituted thienyl group, a substituted or a unsubstituted -CH 2 -(thienyl) group, a substituted or a unsubstituted benzothienyl group, a substituted or a unsubstituted -CH 2 -(benzothienyl) group, a substituted or a unsubstituted furanyl group or a substituted or a unsubstituted -CH 2 -(
  • R 4 preferably is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group or - ⁇ R 3 R 4 taken together is a nitrogen- containing non-aromatic heterocyclic ring, as described in the previous paragraph.
  • Preferred substituents for the nitrogen atom in the piperidinyl group represented by R 4 and recited in this paragraph include R 15 , -C(O)R 15 , -C(0)OR 15 , -C(0)-NHR 15 , -C(0)-N(R 15 ) 2 and -C(0)CH[N(R 16 ) 2 ]R 17 .
  • Yet another preferred embodiment of the present invention is a compound represented by Structural Formulas (XI) or (XIi):
  • Ring A is unsubstituted.
  • Ring B is an unsubstituted phenyl, cyclohexyl or cyclopentyl ring fused to Ring A.
  • R 1 is cyclohexyl or phenyl, furanyl, thienyl or pyridyl optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, methylenedioxy, ethylenedioxy, halogen, cyano, or nitro.
  • R 21 is methyl, ethyl 2-hydroxyethyl or iso-propyl.
  • R 21 indicates that the piperidinyl groups in Structural Formulas (XI) and (XII) are optionally substituted at up to four substitutable carbon atoms with R 21 .
  • a substitutable methylene group in the piperidinyl rings can optionally be substituted with up to two independently selected R 21 s.
  • R 22 is -H or C1-C4 alkyl or -N(R 22 ) 2 taken together is N-pyrollidinyl or N-piperidinyl, provided that R 22 is not -H when R 20 is -COOR 22 .
  • R 23 is -H, methyl or ethyl.
  • R 24 is -H, methyl, ethyl, phenyl, benzyl, 4-hydroxyphenyl or 4-hydroxybenzyl. s is 0, 1, 2, 3, or 4.
  • Also disclosed herein is a compound represented by Structural Formulas (I), (II), (III), (TV), (V), (VI), (VTT), (VD3), (DC), (X), (XI) and (XH) and methods of use thereof for treating a subject with a CCR8 mediated disease or condition and pharmaceutical compositions comprising the same, wherein R 1 has the value corresponding to any one of the compounds in the Tables and Examples of the Exemplification Section and the remainder of the variables are as defined above.
  • aliphatic as used herein means straight-chain or branched hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic.
  • An aliphatic group is typically C ⁇ - 8 , more typically -6.
  • suitable aliphatic groups include substituted or unsubstituted linear or branched alkyl, alkenyl, alkynyl groups and hybrids thereof.
  • alkyl, alkoxy”, “hydroxyalkyl”, “alkoxyalkylene”, and “alkoxycarbonyl”, used alone or as part of a larger moiety includes both straight and branched saturated chains containing one to eight carbon atoms.
  • alkenyl and alkynyl used alone or as part of a larger moiety shall include both straight and branched chains containing two to eight carbon atoms and one or more double and/or triple bonds, respectively.
  • non-aromatic ring used alone or as part of a larger moiety, includes non-aromatic heterocyclic groups and cycloaliphatic groups.
  • cycloaliphatic used alone or as part of a larger moiety, shall include cyclic C 3 -C ⁇ o hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic. Cycloaliphatic groups are typically C 3 - ⁇ o, more typically C 3 - 7 . A "cycloalkyl” is a cyclic aliphatic group that is completely saturated.
  • non-aromatic bridged bicyclic group used alone or as part of a larger moiety, shall include bicyclic ring systems comprising from seven to fifteen ring atoms in which at least three adjacent ring atoms in the bicyclic ring system are shared by both rings.
  • the ring systems can be carbocyclic, in which all ring atoms are carbon, or heterocyclic ("bridged bicyclic non-aromatic heterocyclic groups"), in which one or more ring carbons are replaced with nitrogen, oxygen, sulfur and the like. Examples are shown below:
  • Suitable substituents for substitutable carbon atoms of a non-aromatic bridged bicyclic group are as provided below for non-aromatic heterocyclic groups.
  • Suitable substituents for substitutable nitrogen atoms of a non-aromatic bridged bicyclic group are as provided below for non-aromatic heterocyclic groups.
  • Alkoxy means (alkyl)-O-;
  • alkoxyalkylene means (alkyl)-O-(alkylene) such as methoxymethylene (CH 3 OCH 2 );
  • hydroxyalkyl means hydroxy substituted alkyl group;
  • alkoxy carbonyl means a carbonyl substituted with a carbonyl as in (alkyl)-O-C(O)-; and
  • aralkyl means alkyl substituted with an aromatic group.
  • a "C1-C4 aralkyl group for example, has a C1-C4 alkyl group substituted with an aromatic group.
  • heteroatom means nitrogen, oxygen, or sulfur and includes any oxidized form of nitrogen and sulfur, and the quaternized form of any basic nitrogen.
  • nitrogen includes a substitutable nitrogen of a heterocyclic ring.
  • the nitrogen in a saturated or partially unsaturated ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3,4-dihydro-2H-pyrrolyl), N ⁇ (as in pyrrolidinyl) or NR + (as in N-substituted pyrrolidinyl).
  • aromatic group used alone or as part of a larger moiety as in “aralkyl”, “aralkoxy”, or “aryloxyalkyl”, includes to carbocyclic aromatic ring groups and heteroaryl rings groups.
  • aromatic group may be used interchangeably with the terms “aryl”, “aryl ring” or “aromatic ring”.
  • Carbocyclic aromatic ring groups have only carbon ring atoms and include monocyclic aromatic rings such as phenyl and fused polycyclic aromatic ring systems in which two or more carbocyclic aromatic rings are fused to one another. Examples include 1-naphthyl, 2-naphthyl, 1-anthracyl and 2-anthracyl.
  • Carbocyclic aromatic ring is a group in which an aromatic ring is fused to one or more non-aromatic rings (aliphatic or heterocyclic), such as in an indanyl, phthalimidyl, naphthimidyl, phenantriidinyl, or tetrahydronaphthyl, where the radical or point of attachment is on the aromatic ring.
  • non-aromatic rings aliphatic or heterocyclic
  • heteroaryl used alone or as part of a larger moiety as in “heteroaralkyl” or “heteroarylalkoxy”, refers to heteroaromatic ring groups having five to fourteen members, including monocyclic heteraromatic rings and polycyclic aromatic rings in which a monocyclic aromatic ring is fused to one or more other carbocyclic or heteroaromatic aromatic rings .
  • heteroaryl rings examples include 2-furanyl, 3-furanyl, N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3- isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-oxadiazolyl, 5-oxadiazolyl, 2-oxazolyl, 4- oxazolyl, 5-oxazolyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2- pyrimidyl, 4-pyrimidyl, 5-pyrimidyl, 3-pyridazinyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2- triazolyl, 5-triazolyl, tetrazolyl, 2-thienyl, 3 -thienyl, carbazolyl, benzimidazolyl, benzothienyl, benzofuranyl
  • pyrazolyl is also a suitable value for variables which represent heteroaryl rings.
  • heteroaryl is a group in which a heteroaryl ring is fused to one or more cycloaliphatic or non-aromatic heterocyclic groups where the radical or point of attachment is on the heteroaromatic ring. Examples include tetrahydroquinolinyl, tetrahydroisoquinolinyl, and pyrido [3, 4-d] pyrimidinyl.
  • non-aromatic heterocyclic ring used alone or as part of a larger moiety as in “hetercyclylalkyl”, refers to non-aromatic ring systems typically having five to fourteen members, preferably five to ten, in which one or more ring carbons, preferably one to four, are each replaced by a heteroatom such as ⁇ , O, or S.
  • non- aromatic heterocyclic rings examples include 3-lH-benzimidazol-2-one, 3-tetrahydrofuranyl, 2- tetrahydropyranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, [l,3]-dioxalanyl, [1,3]- dithiolanyl, [l,3]-dioxanyl, 2-tetrahydrothiophenyl, 3-tetrahydrothiophenyl, 2- morpholinyl, 3-morpholinyl, 4-morpholinyl, 2-thiomorpholinyl, 3-thiomorpholinyl, 4- thiomorpholinyl, 1 -pyrrolidinyl, 2-pyrrolidinyl, 3-pyrorolidinyl, 1-piperazinyl, 2- piperazinyl, 1 -piperidinyl, 2-piperidinyl, 3 -piperidinyl, 4-piperidinyl, 4-thiazolidinyl, diazolon
  • the CCR8 inhibitors of the present invention comprise aromatic groups, aliphatic groups and non-aromatic rings, including cycloaliphatic groups and non- aromatic heterocyclic groups, which are optionally substituted, i.e., which comprise one or more substituents.
  • Substituents can be found at one or more substitutable carbon atoms in aromatic groups, aliphatic groups and non-aromatic rings and substitutable nitrogen atoms in heteroaromatic groups and non-aromatic heterocyclic rings.
  • exemplary substituents at the carbon atoms of an aromatic group represented by R 1 are represented by R 10 ; exemplary substituents at the carbon atoms of an aliphatic group represented by R 4 are represented by R 11 ; and exemplary substituents at the carbon atoms of an aromatic group represented by R 4 are represented by R 12 .
  • Suitable values for the substituents represented by R 10 -R 12 and suitable substituents for the substitutable carbon atoms of Rings A and B and for other aromatic groups, aliphatic groups and non-aromatic rings (including cycloaliphatic rings and non- aromatic heterocyclic rings) that form part(s) of the disclosed CCR8 inhibitors are those which do not significantly reduce the compounds ability to antagonize the activity of CCR8 and/or which do not significantly increase toxicity to the subject.
  • Examples include -R°, -OH, -OR 0 , -0(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2- ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -0(Ph), -CH 2 (Ph), substituted -CH 2 (Ph), -CH 2 CH 2 (Ph), substituted -CH 2 CH 2 (Ph), -CN, -NR'C0 2 R°, -NR'NR'C(0)R°, -N(R')C(0)N(R') 2 , -NR'NR'C(0)N(R') 2 , -NR'NR'C0 2 R°, -C(O)C(0)R°, -C(O)CH 2 C(O)R 0 , -C0 2 R°, -C(0)R°, -OC(0)R°, -OC(O)N(R 0
  • R 10 and R n and COOR° is a permissible substituent for the substitutable carbon atoms of an aromatic group represented by R 1 and R 4 and Rings A and B and for other aromatic groups, aliphatic groups and non-aromatic rings that form part(s) of the disclosed CCR8 inhibitors.
  • preferred substituents for aromatic groups, aliphatic groups and non-aromatic rings that form part(s) of the disclosed CCR8 inhibitors are haloalkyl, alkyl, halogen, cyano, nitro, hydroxy, haloalkoxy and alkoxy.
  • Amine, alkylamine and dialkyamine are also a preferred substituents for substitutable carbon atoms of an aliphatic group or a non-aromatic ring of the disclosed CCR8 inhibitors.
  • a substitutable methylene group in an aliphatic or non- aromatic ring permissably has up to two substituents.
  • the carbon atoms of aliphatic groups and non-aromatic rings e.g., a non-aromatic ring represented by R 1 , a non-aromatic heterocyclic group formed from NR 5 (CH m )R 1 , a non- aromatic ring formed from NR 3 R 4 or a non-aromatic ring represented by R 4
  • R 1 a non-aromatic ring represented by R 1
  • R 4 a non-aromatic heterocyclic group formed from NR 5 (CH m )R 1
  • a non- aromatic ring formed from NR 3 R 4 or a non-aromatic ring represented by R 4 are unsubstituted or substituted with an alkyl group, hydroxyalkyl group or halogen.
  • Each R* is independently selected from hydrogen, an unsubstituted aliphatic group or a substituted aliphatic group, preferably from hydrogen or an alkyl group.
  • Each R° is independently hydrogen or substituted or unsubstituted aliphatic group, a substituted or unsubstituted cycloaliphatic group, a substituted or unsubstituted non- aromatic heterocyclic group or a substituted or unsubstituted aromatic group, preferably phenyl group.
  • each R° is independently hydrogen, an alkyl group, a cycloalkyl group, a non-aromatic heterocyclic group or an aromatic group (preferably phenyl).
  • Each R' is independently R°, -C0 2 R°, -S0 2 R° or -C(0)R°.
  • V is a C1-C6 alkylene group.
  • Suitable substituents on the nitrogen of a non-aromatic heterocyclic group include -R + , -N(R + ) 2 , -C(0)R + , -C0 2 R + , -C(0)C(0)R + , -C(0)CH 2 C(0)R + , -S0 2 R + , -S0 2
  • Other examples include -C(0)-NHR + , -C(0)-N(R + ) 2 , -C(0)-CH[N(R + ) 2 ]R + and -C(O)-CH[OR + ]R + .
  • Each R + is independently hydrogen, an aliphatic group, a substituted aliphatic group, phenyl, substituted phenyl, -benzyl, substituted benzyl or an unsubstituted heteroaryl or non-aromatic heterocyclic ring.
  • R + can also be a substituted non-aromatic heterocyclic group and a substituted or unsubstituted cycloaliphatic group; or N(R + ) 2 is a non-aromatic heterocyclic group.
  • substituents on the aliphatic group represented by R examples of substituents on the aliphatic, aromatic, cycloaliphatic or non-aromatic heterocyclic group represented by R° and examples of substituents on the aliphatic group, phenyl group or benzyl group represented by R + include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
  • Electron donating group is a substituent which results in a phenyl ring that has more electron density when the group is present than when it is absent. Electron donating groups have a Hammet sigma value greater than one (see, for example , C. Hansch, A. Leo and D. Hoeckman, "Exploring QSAR Hydrophobic, Electronic and Steric Constants", American Chemical Society (1995), pages 217-32). Examples of electron donating groups include hydroxy, alkoxy, alkyl, alkylamine dialkylamine and amine. Additionally, pharmaceutically acceptable salts of the compounds disclosed herein are also included in the present invention and can be used in the compositions and methods disclosed herein.
  • an acid salt of a compound containing an amine or other basic group can be obtained, by reacting the compound with a suitable organic or inorganic acid, such as hydrogen chloride, hydrogen bromide, acetic acid, perchloric acid and the like.
  • a suitable organic or inorganic acid such as hydrogen chloride, hydrogen bromide, acetic acid, perchloric acid and the like.
  • Compounds with a quaternary ammonium group also contain a counteranion such as chloride, bromide, iodide, acetate, perchlorate and the like.
  • Other examples of such salts include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, tartrates [e.g.
  • Salts of compounds containing a carboxylic acid or other acidic functional group can be prepared by reacting with a suitable base.
  • Such a pharmaceutically acceptable salt may be made with a base which affords a pharmaceutically acceptable cation, which includes alkali metal salts (especially sodium and potassium), alkaline earth metal salts (especially calcium and magnesium), aluminum salts and ammonium salts, as well as salts made from physiologically acceptable organic bases such as trimethylamine, triethylamine, morpholine, pyridine, piperidine, picoline, dicyclohexylamine, N,N'- dibenzylethylenediamine, 2-hydroxyethylamine, bis-(2-hydroxyethyl)amine, tri-(2- hydroxyethy ⁇ )amine, procaine, dibenzylpiperidine, dehydroabietylamine, N,N'- bisdehydroabietylamine, glucamine, N-methylglucamine, collidine, quinine, quinoline, and basic amino acid such as lysine and arginine.
  • a base which affords a pharmaceutically acceptable cation, which
  • CCR8 inhibitors contain one or more chiral centers.
  • the presence of chiral centers in a molecule gives rise to stereoisomers.
  • enantiomers exist for every chiral center in a molecule; and a pair of diastereomers exist for every chiral center in a compound having two or more chiral centers.
  • the present invention encompasses one enantiomer of inhibitor free from the corresponding optical isomer, racemic mixture of the inhibitor and mixtures enriched in one enantiomer relative to its corresponding optical isomer.
  • the mixture contains, for example, an enantiomeric excess of at least 50%, 75%, 90%, 95% 99% or 99.5%.
  • the enantiomers of the present invention may be resolved by methods known to those skilled in the art, for example by formation of diastereoisomeric salts which may be separated, for example, by crystallization; formation of diastereoisomeric derivatives or complexes which may be separated, for example, by crystallization, gas-liquid or liquid chromatography; selective reaction of one enantiomer with an enantiomer-specific reagent, for example enzymatic esterification; or gas-liquid or liquid chromatography in a chiral environment, for example on a chiral support for example silica with a bound chiral ligand or in the presence of a chiral solvent.
  • enantiomers may be synthesized by asymmetric synthesis using optically active reagents, substrates, catalysts or solvents, or by converting one enantiomer into the other by asymmetric transformation.
  • the present invention encompasses a diastereomer free of other diastereomers, a pair of diastereomers free from other diasteromeric pairs, mixtures of diasteromers, mixtures of diasteromeric pairs, mixtures of diasteromers in which one diastereomer is enriched relative to the other diastereomer(s) and mixtures of diasteromeric pairs in which one diastereomeric pair is enriched relative to the other diastereomeric pair(s).
  • the mixture enriched in one diastereomer or diastereomeric pair(s) relative to the other diastereomers or diastereomeric pair(s)
  • the mixture enriched with the depicted or referenced diastereomer or diastereomeric pair(s) relative to other diastereomers or diastereomeric pair(s) for example, by a molar excess of at least 50%, 75%, 90%, 95% 99% or 99.5%.
  • the diastereoisomeric pairs may be separated by methods known to those skilled in the art, for example chromatography or crystallization and the individual enantiomers within each pair may be separated as described above.
  • Example 1 Specific procedures for chromatographically separating diastereomeric pairs of precursors used in the preparation of compounds disclosed herein are provided in Example 1.
  • compounds of the present invention may associated in isolated form with solvent or water, as in a "solvate” or “hydrate”.
  • References to the disclosed compounds or structural formulas depicting the disclosed compounds are meant to include such solvates and hydrates.
  • the disclosed compounds, pharmaceutical compositions and methods can be used to inhibit CCR8 activity, to inhibit 1-309 activity and to inhibit or treat (therapeutically or prophylactically) conditions mediated by CCR8 and/or 1-309, including inflammatory disorders and allergic conditions.
  • the disclosed compounds can also be advantageously used to inhibit conditions mediated by esinophils and monocytes, T lymphocytes and other immune system cells which express CCR8, including inflammatory disorders and allergic mediated by these cells.
  • allergic conditions for which the disclosed compounds, pharmaceutical compositions and methods are particularly effective include asthma.
  • Other allergic conditions which are expected to be treatable by inhibiting CCR8 activity include, atopic dermatitis, allergic rhinitis, systemic anaphylaxis or hypersensitivity responses, drug allergies (e.g., to penicillin, cephalosporins), insect sting allergies and dermatoses such as dermatitis, eczema, atopic dermatitis, allergic contact dermatitis and urticaria.
  • diseases with an inflammatory component for which the disclosed compounds, pharmaceutical composition and methods are effective include rheumatoid arthritis, osteoarthritis, inflammatory bowel disease [e.g., such as ulcerative colitis, Crohn's disease, ileitis, Celiac disease, nontropical Sprue, enteritis, enteropathy associated with serorlegative arthropathies, microscopic or collagenous colitis, eosinophilic gastroenteritis, or pouchitis resulting after proctocolectomy, and ileoanal anastomosis] and disorders of the skin [e.g., psoriasis, erythema, pruritis, and acne].
  • inflammatory bowel disease e.g., such as ulcerative colitis, Crohn's disease, ileitis, Celiac disease, nontropical Sprue, enteritis, enteropathy associated with serorlegative arthropathies, microscopic or collagenous colitis, eosinophilic gastroenteritis
  • autoimmune diseases also have an inflammatory component.
  • examples include multiple sclerosis, systemic lupus erythematosus, myasthenia gravis, juvenile onset diabetes, glomerulonephritis and other nephritides, autoimmune thyroiditis, Behcet's disease and graft rejection (including allograft rejection or graft-versus-host disease).
  • the inflammatory component of these disorders is believed to be mediated, at least in part, by CCR8.
  • Diseases characterized by repurfusion have an inflammatory component that is believed to be mediated, at least in part by CCR8. Examples include stroke, cardiac ischemia, and the like.
  • the disclosed compounds and compositions also can be used to treat these disorders.
  • CCR8 diseases and conditions with an inflammatory component believed to be mediated by CCR8 include mastitis (mammary gland), vaginitis, cholecystitis, cholangitis or pericholangitis (bile duct and surrounding tissue of the liver), chronic bronchitis, chronic sinusitis, chronic inflammatory diseases of the lung which result in interstitial fibrosis, such as interstitial lung diseases (ILD) (e.g., idiopathic pulmonary fibrosis, or ILD associated with rheumatoid arthritis, or other autoimmune conditions), hypersensitivity pneumonitis, collagen diseases and sarcoidosis.
  • ILD interstitial lung diseases
  • vasculitis e.g., necrotizing, cutaneous, and hypersensitivity vasculitis
  • spondyloarthropathies e.g., spondyloarthropathies
  • scleroderma e.g., atherosclerosis
  • restenosis e.g., restenosis
  • myositis including polymyositis, dermatomyositis
  • pancreatitis e.g., pancreatitis and insulin-dependent diabetes mellitus.
  • a subject with a condition having one or more symptoms mediated by CCR8, including one of the aforementioned diseases or conditions is said "to be in need of CCR8 inhibition”.
  • the subject with a disease or condition of this type is "treated” when at least one of the symptoms associated with the disease or condition is alleviated (therapeutic treatment) or inhibited or prevented (prophylactic treatment), in whole or in part.
  • a "subject” is a mammal, preferably a human, but can also be an animal in need of veterinary treatment, e.g., companion animals (e.g., dogs, cats, and the like), farm animals (e.g., cows, sheep, pigs, horses, and the like) and laboratory animals (e.g., rats, mice, guinea pigs, and the like).
  • companion animals e.g., dogs, cats, and the like
  • farm animals e.g., cows, sheep, pigs, horses, and the like
  • laboratory animals e.g., rats, mice, guinea pigs, and the like.
  • a "subject in need of CCR8 inhibition” is a subject in whom a beneficial therapeutic or prophylactic effect can be achieved by inhibiting CCR8 function or activity.
  • an "effective amount" of the disclosed CCR8 inhibitors is the quantity which inhibits CCR8 activity in a subject in need of such inhibition, or which, when administered to a subject with a CCR8 mediated condition or disease, ameliorates the symptoms of the disease, delays the onset of the symptoms and/or increases longevity.
  • CCR8 inhibitor administered to the subject will depend on the type and severity of the disease or condition and on the characteristics of the subject, such as general health, age, sex, body weight and tolerance to drugs.
  • the dosage may also vary according to the route of administration, which includes oral, aerosol, rectal, transdermal, subcutaneous, intravenous, intramuscular, intraperitoneal and intranasal.
  • An "effective amount” typically ranges between about 0.01 mg/kg/day to about 100 mg/kg/day, preferably between about 0.5 mg/kg/day to about 50 mg/kg/day.
  • the CCR8 inhibitors described herein, and the pharmaceutically acceptable salts thereof can be used in pharmaceutical preparations in combination with a pharmaceutically acceptable carrier or diluent. Suitable pharmaceutically acceptable carriers include inert solid fillers or diluents and sterile aqueous or organic solutions. The CCR8 inhibitor will be present in such pharmaceutical compositions in amounts sufficient to provide the desired dosage amount in the range described herein. Techniques for formulation and administration of the compounds of the instant invention can be found in Remington: the Science and Practice of Pharmacy, 19 th edition, Mack Publishing Co., Easton, PA (1995).
  • the CCR8 inhibitor or salts thereof can be combined with a suitable solid or liquid carrier or diluent to form capsules, tablets, pills, powders, syrups, solutions, suspensions and the like.
  • the tablets, pills, capsules, and the like contain from about 1 to about 99 weight percent of the active ingredient and a binder such as gum tragacanth, acacias, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid, a lubricant such as magnesium stearate; and a sweetening agent such as sucrose lactose or saccharin.
  • a dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier such as a fatty oil.
  • tablets may be coated with shellac, sugar or both.
  • a syrup or elixir may contain, in addition to the active ingredient, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and a flavoring such as cherry or orange flavor.
  • the disclosed CCR8 inhibitor, or salts thereof can be combined with sterile aqueous or organic media to form injectable solutions or suspensions.
  • aqueous or organic media for example, solutions in sesame or peanut oil, aqueous propylene glycol and the like can be used, as well as aqueous solutions of water-soluble pharmaceutically- acceptable salts of the compounds.
  • Dispersions can also be prepared in glycerol, liquid polyethylene glycols and mixtures thereof in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.
  • the compounds may also be formulated as a depot preparation.
  • Such long acting formulations may be administered by implantation, for example, subcutaneously or intramuscularly or by intramuscular injection.
  • implantation for example, subcutaneously or intramuscularly or by intramuscular injection.
  • ion exchange resins for example, as an emulsion in an acceptable oil, or ion exchange resins, or as sparingly soluble derivatives, for example, as sparingly soluble salts.
  • a terminal methyl group in a compound described herein can be shown as a straight line with or without "CH3" on its terminus:
  • the present invention is directed to a compound represented by Structural Formulas (I), (TT) or (ITT) (and methods of use thereof), provided that when R 1 is pyridyl and R 4 is a phenyl group, then the phenyl group represented by R 4 is substituted with a group other than -NO 2 , -NR X R X , -CONR x R x , -NR x COR x , or an aliphatic group substituted with -NO 2 , -NR x R x , -CONR x R x or -NR x COR x .
  • Each R x is independently H, an aliphatic group, a substituted aliphatic group, an aryl group a substituted aryl group, a non-aromatic ring or a substituted non-aromatic ring.
  • the subject matter encompassed by Structural Formlas (I)-(IH) excludes N-[4-[[(4- methoxyphenyl)amino] sulfonyl] - 1 -naphthalenyl] -benzamide, N-[4-[(2-propenylamino)sulfonyl]-l-naphthalenyl]-benzamide, N-[4-(4-morpholinylsulfonyl)-l-naphthalenyl]-benzamide or N-[4-( 1 -piperidinylsulfonyl)- 1 -naphthalenyl] -benzamide .
  • the invention is illustrated by the following examples which are
  • LC/MS spectra were obtained using a MicroMass Platform LC (Phenomenx C18 column, 5 micron, 50 x 4.6 mm) equipped with a Gilson 215 Liquid Handler. Standard LC/MS conditions are as follows: Formic acid-Standard conditions:
  • the titled compound was made following the procedure in Scheme 1-1.
  • the oxime (prepared as detailed in Scheme 1-1) (2.5 g) was dissolved in MeOH (10 mL) and AcOH (2 mL) and Pt0 2 (100 mg) were added at the resultant mixture stirred at room temperature.
  • the reaction mixture was shaken for 2 days at 60 psi under an atmosphere of H 2 .
  • the resultant solution was filtered and concentrated to give the crude product of racemic 3-amino-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid ethyl ester. It was used without further purification.
  • N-[4-(3-Methoxy-phenylsulfamoyI)-naphthalen-l-yl]-benzamide (A-l) To a solution of 4-benzoylamino-naphthalene-l-sulfonyl chloride (320 mg, 0.93 mmol) in CH 2 C1 2 (20 mL) was added triethylamine (0.26 mL, 1.85 mmol) and m- anisidine (137 mg, 1.11 mmol). The resultant solution was stirred at 25 °C overnight. The reaction mixture was quenched with water and extracted with CH 2 C1 2 .
  • A-21 1H ⁇ MR (300 MHz, CDC1 3 ) ⁇ 8.73 (d, IH), 8.35 (m, 2H), 8.11 (s, IH), 7.93 (d, IH), 7.65 (m, 3H), 7.44 (m, IH), 7.33 (d, TTT), 7.23(m, 5H), 4.70 (d, IH), 3.38 (q, 2H), 3.29 (m, IH), 2.58 (s, 3H), 2.25 (br s, 2H), 1.75 (m, IH), 1.48 (m, 2H), 0.97 (d, IH); 0.65 (d, 3H); LC/MS m/z 528 (M + H) + .
  • A-23 * H ⁇ MR (300 MHz, CDC1 3 ) ⁇ 8.70 (d, IH), 8.32 (s, IH), 8.25 (s, 2H), 7.93 (d, IH), 7.60 (m, 3H), 7.40 (m, IH), 7.25 (m, 6H), 4.78 (d, IH), 3.38 (q, 2H), 2.72 (m, 2H), 2.55 (s, 3H), 2.24 (m, IH), 1.86 (m, IH), 1.63 (m, 3H), 1.35 (m, 2H); 0.57 (d, 3H); LC/MS m/z 528 (M + H) + .
  • A-47 and A-48 were obtained.
  • A-49 and A-50 formic acid salts were obtained.
  • 4-(4-Benzoylamino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert- butyl ester (11) was prepared following the general procedure in Scheme 2. To a solution of 4-(4-benzoylamino-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester (11) in MeOH was added a solution of 4 ⁇ HCl in dioxane. The reaction mixture was stirred at 25 °C for 5 h and then concentrated in vacuo. The crude material was purified by reverse phase HPLC to provide the title compound.
  • the title compound was prepared from A-21 according to the general procedure in Scheme 7. To a solution of A-21 in ethyl acetate was added Pd(OH) 2 and diethyl pyrocarbonate (1.0 eq). The vessel was evacuated and pressurized to 50 psi H and allowed to agitate on a Parr apparatus overnight. The solution was filtered through a celite plug, washed with hot ethyl acetate and concentrated at 40°C at reduced pressure. The residue was purified using flash chromatography to provide the title compound.
  • 4-(4-Amino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester (20) was prepared according to the general procedure in Scheme 3 substituting 4-[4-( 1 ,3 -dioxo- 1 ,3 -dihydro-isoindol-2-yl)-naphthalene- 1 -sulfonylamino] - piperidine- 1 -carboxylic acid tert-butyl ester for 4-(l,3-dioxo-l,3-dihydro-isoindol-2- yl)-naphthalene-l -sulfonic acid (4-methoxyphenyl)-amide.
  • Method B To neat amide (22), at 0°C, was added chlorosulfonic acid (5 eq) dropwise. The temperature was allowed to warm to 25 °C and then heated at 70°C for 45 minutes. After cooling to 25 °C, the reaction mixture was poured into ice water, and the resultant precipitate was collected by filtration to give the title sulfonyl chloride as a white solid. The product was used without further purification.

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Abstract

Disclosed is an inhibitor of CCR8 that is represented by Structural Formula (I). Also disclosed are pharmaceutical compositions comprising a pharmaceutically acceptable carrier or diluent and a CCR8 inhibitor represented by Structural Formula (I). Also disclosed is a method of treating inflammatory disorders in a subject by administering a CCR8 inhibitor to the subject.

Description

CCR8 INHIBITORS RELATED APPLICATION
This application claims the benefit of U.S. Provisional Application No. 60/436,508, filed on December 23, 2002. The entire teachings of the above application(s) are incorporated herein by reference.
BACKGROUND OF THE INVENTION
Chemoattractant cytokines or chemokines are a family of proinflammatory mediators that promote recruitment and activation of multiple lineages of leukocytes and lymphocytes. They can be released by many kinds of tissue cells after activation. Continuous release of chemokines at sites of inflammation mediates the ongoing migration of effector cells in chronic inflammation (Baggiolini, et. al, Nature 15:365 (1994)). Indeed, chemokines have been implicated in a wide range of human acute and chronic inflammatory diseases including, but not limited to, respiratory diseases such as asthma, inflammatory bowel disease, allergic disorders and certain autoimmune diseases such as rheumatoid arthritis.
Chemokines exert their biological activity by binding to specific G-protein receptors, which then transduce signals important for the development and trafficking of specific leukocyte subsets (Baggiolini, et. al, Nature 15:365 (1994)). A number of chemokine receptors have been characterized and each are differentially expressed among leukocyte populations. Significantly, each chemokine binds specifically to a single receptor or to a small group of receptors. Thus, the recruitment and activation of specific classes of leukocytes or lymphocytes can be modulated by agents which selectively act at one chemokine receptor and/or block the activity of a specific chemokine. Agents which selectively block the activity of a specific chemokine or chemokine receptor are therefore useful in treating inflammatory diseases caused by aberrant activation of leukocytes or lymphocytes which express those chemokine receptors (or are activated by the chemokine) and minimally affect immune system cells which express other chemokine receptors. CCR8 is a chemokine receptor (see WO 99/065561) whose expression is primarily restricted to Th2 cells (Zingoni et al, J. Immunol. 161:541 (1998) and D'Ambrosio et al, J. Immunol. 161:5111 (1998)). 1-309 is a ligand for CCR8 and has shown to be chemotactic for the cells in vitro (D'Ambrosio et al, J. Immunol 161:5111 (1998). CCR8 is also involved in eosinophil recruitment (see WO 99/065561). Thus, antagonists for CCR8 are expected to be useful in treating disorders mediated by Th2 and eosinophil cells, e.g., asthma.
SUMMARY OF THE INVENTION
Disclosed herein are 1,4-naphthylsulfonamides, also referred to herein as "1,4- naphthylene sulfonamides", which are effective inhibitors of CCR8 activity. For example, most of the naphthylsulfonamides shown in the Tables at the end of the Experimental Section inhibit CCR8 activity with a Kj less than 1 μM. Based on this discovery, novel CCR8 inhibitors, pharmaceutical compositions comprising these inhibitors and methods of treating inflammatory disorders with these inhibitors are disclosed herein.
One embodiment of the present invention is a compound (a CCR8 inhibitor) represented by Structural Formula (I):
Figure imgf000003_0001
X is a covalent bond, O or NR .
Xi is a covalent bond, C=O or CRaRb. In one preferred embodiment, Xi is a covalent bond; in another preferred embodiment, Xi is CH2.
C=Z is C=0, CH2, C=NH, C=S or absent, provided that when Xi is a covalent bond then C=Z is not CH2. Preferably, when C=Z is absent then X is a covalent bond, and when X is NR5 and C=Z is C=0 then R4 is not an aliphatic or substituted aliphatic group. More preferably, C=Z is C=0, CH2, C=NH or C=S, provided that when Xi is a covalent bond then C=Z is not CH2. Even more preferably C=Z is C=O or C=S.
Ra and Rb are independently -H or a C1-C3 alkyl.
R1 is a substituted or unsubstituted aromatic group or a substituted or unsubstituted non-aromatic ring. Alternatively, when X is NR5, then -NR5(CH2)mR1, taken together, is optionally a substituted or unsubstituted non-aromatic heterocyclic group.
R2 is -H or a C1-C3 alkyl group.
R3 is -H and R4 is a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group, a substituted or unsubstituted non-aromatic ring or a substituted or substituted non-aromatic bridged bicyclic group (preferably, a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group, a substituted or unsubstituted non-aromatic ring, more preferably, a substituted or unsubstituted aromatic group, or a substituted or unsubstituted non-aromatic ring) or, R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group.
R5 is -H, or a C1-C3 alkyl group.
Rings A and B are independently substituted or unsubstituted.
Ring B is a phenyl ring or a five or six membered carbocyclic carbocyclic non- aromatic ring fused to Ring A. Preferably, Ring B is an optionally substituted phenyl or optionally substituted six membered non-aromatic carbocyclic ring (e.g., cyclohexyl or cyclohexenyl) fused to Ring A. m is 0, 1, 2 or 3. n is 1 or 2.
Another embodiment of the present invention method is a method of treating a subject with a CCR8 mediated condition or disease, e.g., a subject with asthma. The method comprises the step of administering to the subject an effective amount of a CCR8 inhibitor disclosed herein.
Yet another embodiment of the present invention is a pharmaceutical composition. The pharmaceutical composition comprises a pharmaceutically acceptable carrier or diluent and a CCR8 inhibitor disclosed herein. The pharmaceutical compositions can be used in therapy, for example, to treat a subject with a CCR8 mediated condition or disease, for example, a subject with asthma.
Yet another embodiment of the present invention is the use of one of the disclosed CCR8 inhibitors for the manufacture of a medicament for treating a subject with a CCR8 mediated condition or disease. The medicament comprises an effective amount of the CCR8 inhibitor.
The disclosed compounds are effective inhibitors of CCR8 and, as such, are expected to be useful in the treatment and prevention of diseases mediated by CCR8, particularly asthma. Other diseases for which the disclosed CCR8 inhibitors are expected to be effective include, but not limited to, inflammatory diseases such as atopic dermatitis, allergic rhinitis, systemic anaphylaxis or hypersensitivity responses, drug allergies (e.g., to penicillin, cephalosporins), insect sting allergies and inflammatory dermatoses such as dermatitis, eczema, allergic contact dermatitis, urticaria, atherosclerosis, restenosis and myositis (including polymyositis, dermatomyositis).
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to inhibitors of the chemokine receptor commonly referred to as "CCR8". CCR8 is expressed on monocytes and Th2 lymphocytes and in the brain, spleen and thymus. It is the receptor for the chemokine I- 309, which is chemotactic for Th2 cells. 1-309 has also shown to be involved in esinophil recruitment. Thus, the disclosed compounds can be used to inhibit CCR8 activity; to inhibit 1-309 activity and to inhibit or treat (therapeutically or prophylactically) conditions mediated by CCR8 and/or 1-309, including inflammatory disorders and allergic conditions. The disclosed compounds can also be advantageously used to inhibit conditions mediated by esinophils and by monocytes, T lymphocytes and other immune system cells which express CCR8, including inflammatory disorders and allergic conditions mediated by these cells.
The compound represented by Structural Formula (I) is preferably characterized by one, two, three or more of the following features: (1) C=Z is C=0 and Xi is a bond or C=Z is CH2 and Xi is CRaRb ; (2) X is a bond; (3) R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more substituent groups, e.g., the substituent groups represented by R10; (4) R2 is -H; (5) R3 is -H or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; (6) R4 is a substituted or unsubstituted non-aromatic ring or a phenyl or benzyl group optionally substituted with one or more substituent groups, e.g., the substituent groups represented by R12; (7) m is 0 or 1; and (8) n is 2. Exemplary values for R10 and R12 are provided below in the section describing suitable aromatic and aliphatic group substituents. Commonly, the compound is characterized by features (1); (2); (3); (4); (5); (6); (7); (8); (1) and (4); (1), (2) and (4); (1), (3) and (4); (1), (4) and (5); (1), (4), and (6); (1), (4) and (7); (1), (4) and (8); (1), (4), (7) and (8); (1), (2), (4), (7) and (8); (1), (3), (4), (7) and (8); (1), (4), (5), (7) and (8); (1), (4), (6), (7) and (8); (1), (2), (3), (4), (5), (7) and (8); (1), (2), (4), (5), (6), (7) and (8); and (1), (3), (4), (5), (6), (7) and (8). Preferably, the compound represented by Structural Formula (I) is characterized by all of Features (l)-(8).
Alternatively, the compound represented by Structural Formula (I) is characterized as described in the previous paragraph, except that Xi is C=0 and C=Z is absent for feature (1).
In one preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (TT):
Figure imgf000006_0001
(II).
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (ITI):
Figure imgf000007_0001
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (IV):
Figure imgf000007_0002
i another preferred embodiment, the CCR8 inhibitor is represented by Structural
Formula (V):
Figure imgf000007_0003
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (VI):
Figure imgf000008_0001
(VI).
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (VH):
Figure imgf000008_0002
(VH).
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (Vm):
Figure imgf000008_0003
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (DC):
Figure imgf000009_0001
(IX)
In another preferred embodiment, the CCR8 inhibitor is represented by Structural Formula (X):
Figure imgf000009_0002
(X).
In Structural Formulas (II)-(X), R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more groups, for example, the substituent groups represented by R10; R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups, for example the substituent groups represented by R12 or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1; and Rings A and B are optionally and independently substituted at any one or more substitutable ring carbons. Exemplary values for R10 and R12 and exemplary substituents for Rings A and B are provided hereinbelow in the section describing aromatic group and non- aromatic ring substituents. Preferred substituents for Rings A and B include alkyl, haloalkyl, alkoxy, haloalkoxy, hydroxy, halogen, cyano and nitro. Preferably, Rings A and B are unsubstituted. One preferred value for R4 in Structural Formulas (I)-(X) is a substituted or unsubstituted non-aromatic ring. Suitable substituents for a non-aromatic ring represented by R4 are provided hereinbelow in section describing substituents for a substitutable carbon on a non-aromatic ring and in the section describing substituents for the nitrogen atom of a non-aromatic heterocyclic group. When R4 in Structural Formulas (I)-(X) is a non-aromatic ring, preferred values include a piperidinyl group, an N-substituted piperidinyl group, or a cyclohexyl group. Suitable substituents for the nitrogen atom in a piperidinyl group represented by R4 are provided hereinbelow in the section describing substituents on the nitrogen atom of a non-aromatic heterocyclic group. Preferred substituents for the nitrogen atom in a piperidinyl group represented by R4 include R15, -C(0)R15, -C(0)OR15, and -C(0)-ΝHR15. Other preferred substituents for the nitrogen atom in a piperidinyl group represented by R4 include -C(0)-N(R15)2 or -C(0)CH[N(R16)2]R17. R15 is -H, a non-aromatic ring, or a substituted or unsubstituted aliphatic group or a substituted or unsubstituted C7-C9 aralkyl group. Typically, however, -C(0)ORls is not -COOH. R15 can also be a substituted or unsubstituted non-aromatic ring. In addition, N(R15)2 taken together can be a substituted or unsubstituted five or six membered non-aromatic nitrogen-containing heterocyclic group. Preferred substituents for a substitutable carbon of the non-aromatic ring represented by R15 or the non-aromatic heterocyclic group represented by N(R15)2 included methyl, ethyl hydroxyethyl and iso- propyl; suitable substituents for a substitutable nitrogen of these groups include alkyl, alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl and dialkylaminocarbonyl. R16 is -H or an alkyl group. R17 is -H; a C1-C6 alkyl group optionally substituted with -OH, -NH2, phenyl or phenyl substituted with -OH; indolyl; imidazolyl; or phenyl optionally substituted with -OH.
Another preferred value for R4 in Structural Formulas (I)-(X) is a phenyl group, a substituted phenyl group, a benzyl group or a substituted benzyl group. Suitable substituents for phenyl and benzyl groups represented by R4 are provided hereinbelow in the section describing suitable aromatic group substituents. Preferred substituents are electron donating groups such as methoxy, ethoxy, iso-propoxy, methyl, ethyl, propyl, NH2, NHCH3, N(CH3)2, NHCH2CH3, N(CH2CH3)2, N(CH3)(CH2CH3), NH(CH2CH2CH3), N(CH2CH2CH3)2, N(CH3)(CH2CH2CH3) or N(CH2CH3)(CH2CH2CH3).
In another preferred embodiment, -NR3R4 in Structural Formulas (I)-(X), taken together, is a substituted or unsubstituted rion-aromatic heterocyclic group. Suitable substituents for a non-aromatic heterocyclic group represented by -NR3R4 are provided hereinbelow in section describing suitable substituents for a substitutable carbon of a non- aromatic group and in the section describing suitable substituents for the nitrogen atom of a non-aromatic heterocyclic group.
In Structural Formulas (I)-(X), R1 is preferably a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or a unsubstituted -CH2-(pyridyl) group, a substituted or a unsubstituted thienyl group, a substituted or a unsubstituted -CH2-(thienyl) group, a substituted or a unsubstituted benzothienyl group, a substituted or a unsubstituted -CH2-(benzothienyl) group, a substituted or a unsubstituted furanyl group or a substituted or a unsubstituted -CH2-(furanyl) group and more preferably is an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group. When R1 has these values, then R4 preferably is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group or -ΝR3R4 taken together is a nitrogen- containing non-aromatic heterocyclic ring, as described in the previous paragraph.
Preferred substituents for the nitrogen atom in the piperidinyl group represented by R4 and recited in this paragraph include R15, -C(O)R15, -C(0)OR15, -C(0)-NHR15, -C(0)-N(R15)2 and -C(0)CH[N(R16)2]R17.
Also disclosed is a compound represented by Structural Formula (TT) or (ITT) wherein the amide group connected to the napthyl ring is replaced with a carbamate (-O- C(O)NH-), a thiocarbamate (-O-C(S)NH-), a urethane (NH-C(O)-NH-) or a thiourethane group (NH-C(S)-NH-).
Yet another preferred embodiment of the present invention is a compound represented by Structural Formulas (XI) or (XIi):
Figure imgf000012_0001
The variables in Structural Formulas (XI) and (XII) are defined below.
Ring A is unsubstituted.
Ring B is an unsubstituted phenyl, cyclohexyl or cyclopentyl ring fused to Ring A.
R1 is cyclohexyl or phenyl, furanyl, thienyl or pyridyl optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, methylenedioxy, ethylenedioxy, halogen, cyano, or nitro.
Figure imgf000012_0002
-C(0)-NHR22, -C(0)-N(R22)2 or -C(0)CH[N(R23)2]R24.
R21 is methyl, ethyl 2-hydroxyethyl or iso-propyl. R21 indicates that the piperidinyl groups in Structural Formulas (XI) and (XII) are optionally substituted at up to four substitutable carbon atoms with R21. A substitutable methylene group in the piperidinyl rings can optionally be substituted with up to two independently selected R21s.
R22 is -H or C1-C4 alkyl or -N(R22)2 taken together is N-pyrollidinyl or N-piperidinyl, provided that R22 is not -H when R20 is -COOR22. R23 is -H, methyl or ethyl.
R24 is -H, methyl, ethyl, phenyl, benzyl, 4-hydroxyphenyl or 4-hydroxybenzyl. s is 0, 1, 2, 3, or 4.
Also disclosed herein is a compound represented by Structural Formulas (I), (II), (III), (TV), (V), (VI), (VTT), (VD3), (DC), (X), (XI) and (XH) and methods of use thereof for treating a subject with a CCR8 mediated disease or condition and pharmaceutical compositions comprising the same, wherein R1 has the value corresponding to any one of the compounds in the Tables and Examples of the Exemplification Section and the remainder of the variables are as defined above.
Also disclosed herein is a compound represented by Structural Formulas (I), (TT), (III), (IV), (V), (VI), (VTT), (Vffl), (DC), (X), (XI) and (XII) and methods of use thereof for treating a subject with a CCR8 mediated disease or condition and pharmaceutical compositions comprising the same, wherein NR3R4 has the value corresponding to any one of the compounds in the Tables and Examples of the Exemplification Section and the remainder of the variables are as defined above. Also disclosed is a compound represented by Structural Formulas (I), (H), (JIT),
(IV), (V), (VI), (VH), (Vπi), (DC), (X), (XI) and (XH) and methods of use thereof for treating a subject with a CCR8 mediated disease or condition and pharmaceutical compositions comprising the same, wherein R3 is -H and R4 is a substituted or unsubstituted aromatic group or a substituted or unsubstituted non-aromatic ring, or -NR3R is a substituted or unsubstituted non-aromatic heterocyclic group, and the remainder of the variables are as described above.
The term "aliphatic" as used herein means straight-chain or branched hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic. An aliphatic group is typically Cι-8, more typically -6. For example, suitable aliphatic groups include substituted or unsubstituted linear or branched alkyl, alkenyl, alkynyl groups and hybrids thereof. The terms "alkyl", "alkoxy", "hydroxyalkyl", "alkoxyalkylene", and "alkoxycarbonyl", used alone or as part of a larger moiety includes both straight and branched saturated chains containing one to eight carbon atoms. The terms "alkenyl" and alkynyl" used alone or as part of a larger moiety shall include both straight and branched chains containing two to eight carbon atoms and one or more double and/or triple bonds, respectively.
The term "non-aromatic ring", used alone or as part of a larger moiety, includes non-aromatic heterocyclic groups and cycloaliphatic groups.
The term "cycloaliphatic" used alone or as part of a larger moiety, shall include cyclic C3-Cιo hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic. Cycloaliphatic groups are typically C3-ιo, more typically C3-7. A "cycloalkyl" is a cyclic aliphatic group that is completely saturated.
The teπn "non-aromatic bridged bicyclic group", used alone or as part of a larger moiety, shall include bicyclic ring systems comprising from seven to fifteen ring atoms in which at least three adjacent ring atoms in the bicyclic ring system are shared by both rings. The ring systems can be carbocyclic, in which all ring atoms are carbon, or heterocyclic ("bridged bicyclic non-aromatic heterocyclic groups"), in which one or more ring carbons are replaced with nitrogen, oxygen, sulfur and the like. Examples are shown below:
Figure imgf000014_0001
Figure imgf000015_0001
Suitable substituents for substitutable carbon atoms of a non-aromatic bridged bicyclic group are as provided below for non-aromatic heterocyclic groups. Suitable substituents for substitutable nitrogen atoms of a non-aromatic bridged bicyclic group are as provided below for non-aromatic heterocyclic groups.
"Alkoxy" means (alkyl)-O-; "alkoxyalkylene" means (alkyl)-O-(alkylene) such as methoxymethylene (CH3OCH2); "hydroxyalkyl" means hydroxy substituted alkyl group; "alkoxy carbonyl means a carbonyl substituted with a carbonyl as in (alkyl)-O-C(O)-; and "aralkyl" means alkyl substituted with an aromatic group. A "C1-C4 aralkyl group", for example, has a C1-C4 alkyl group substituted with an aromatic group.
The term "heteroatom" means nitrogen, oxygen, or sulfur and includes any oxidized form of nitrogen and sulfur, and the quaternized form of any basic nitrogen. Also the term "nitrogen" includes a substitutable nitrogen of a heterocyclic ring. As an example, in a saturated or partially unsaturated ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3,4-dihydro-2H-pyrrolyl), NΗ (as in pyrrolidinyl) or NR+ (as in N-substituted pyrrolidinyl).
The term "aromatic group" used alone or as part of a larger moiety as in "aralkyl", "aralkoxy", or "aryloxyalkyl", includes to carbocyclic aromatic ring groups and heteroaryl rings groups. The term "aromatic group" may be used interchangeably with the terms "aryl", "aryl ring" or "aromatic ring".
Carbocyclic aromatic ring groups have only carbon ring atoms and include monocyclic aromatic rings such as phenyl and fused polycyclic aromatic ring systems in which two or more carbocyclic aromatic rings are fused to one another. Examples include 1-naphthyl, 2-naphthyl, 1-anthracyl and 2-anthracyl. Also included within the scope of the term "carbocyclic aromatic ring", as it is used herein, is a group in which an aromatic ring is fused to one or more non-aromatic rings (aliphatic or heterocyclic), such as in an indanyl, phthalimidyl, naphthimidyl, phenantriidinyl, or tetrahydronaphthyl, where the radical or point of attachment is on the aromatic ring.
The term "heteroaryl", "heteroaromatic" or "heteroaryl ring", used alone or as part of a larger moiety as in "heteroaralkyl" or "heteroarylalkoxy", refers to heteroaromatic ring groups having five to fourteen members, including monocyclic heteraromatic rings and polycyclic aromatic rings in which a monocyclic aromatic ring is fused to one or more other carbocyclic or heteroaromatic aromatic rings . Examples of heteroaryl rings include 2-furanyl, 3-furanyl, N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3- isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-oxadiazolyl, 5-oxadiazolyl, 2-oxazolyl, 4- oxazolyl, 5-oxazolyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2- pyrimidyl, 4-pyrimidyl, 5-pyrimidyl, 3-pyridazinyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2- triazolyl, 5-triazolyl, tetrazolyl, 2-thienyl, 3 -thienyl, carbazolyl, benzimidazolyl, benzothienyl, benzofuranyl, indolyl, quinolinyl, benzotriazolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoquinolinyl, indolyl, isoindolyl, acridinyl, or benzoisazolyl. Other than R°, pyrazolyl is also a suitable value for variables which represent heteroaryl rings. Also included within the scope of the term "heteroaryl", as it is used herein, is a group in which a heteroaryl ring is fused to one or more cycloaliphatic or non-aromatic heterocyclic groups where the radical or point of attachment is on the heteroaromatic ring. Examples include tetrahydroquinolinyl, tetrahydroisoquinolinyl, and pyrido [3, 4-d] pyrimidinyl.
The term "non-aromatic heterocyclic ring", used alone or as part of a larger moiety as in "hetercyclylalkyl", refers to non-aromatic ring systems typically having five to fourteen members, preferably five to ten, in which one or more ring carbons, preferably one to four, are each replaced by a heteroatom such as Ν, O, or S. Examples of non- aromatic heterocyclic rings include 3-lH-benzimidazol-2-one, 3-tetrahydrofuranyl, 2- tetrahydropyranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, [l,3]-dioxalanyl, [1,3]- dithiolanyl, [l,3]-dioxanyl, 2-tetrahydrothiophenyl, 3-tetrahydrothiophenyl, 2- morpholinyl, 3-morpholinyl, 4-morpholinyl, 2-thiomorpholinyl, 3-thiomorpholinyl, 4- thiomorpholinyl, 1 -pyrrolidinyl, 2-pyrrolidinyl, 3-pyrorolidinyl, 1-piperazinyl, 2- piperazinyl, 1 -piperidinyl, 2-piperidinyl, 3 -piperidinyl, 4-piperidinyl, 4-thiazolidinyl, diazolonyl, N-substituted diazolonyl, 1-pthalimidinyl, benzoxanyl, benzopyrrolidinyl, benzopiperidinyl, benzoxolanyl, benzothiolanyl, and benzothianyl.
As noted above, the CCR8 inhibitors of the present invention comprise aromatic groups, aliphatic groups and non-aromatic rings, including cycloaliphatic groups and non- aromatic heterocyclic groups, which are optionally substituted, i.e., which comprise one or more substituents. Substituents can be found at one or more substitutable carbon atoms in aromatic groups, aliphatic groups and non-aromatic rings and substitutable nitrogen atoms in heteroaromatic groups and non-aromatic heterocyclic rings. For ease of reference, exemplary substituents at the carbon atoms of an aromatic group represented by R1 are represented by R10; exemplary substituents at the carbon atoms of an aliphatic group represented by R4 are represented by R11; and exemplary substituents at the carbon atoms of an aromatic group represented by R4 are represented by R12.
Suitable values for the substituents represented by R10-R12 and suitable substituents for the substitutable carbon atoms of Rings A and B and for other aromatic groups, aliphatic groups and non-aromatic rings (including cycloaliphatic rings and non- aromatic heterocyclic rings) that form part(s) of the disclosed CCR8 inhibitors are those which do not significantly reduce the compounds ability to antagonize the activity of CCR8 and/or which do not significantly increase toxicity to the subject. Examples include -R°, -OH, -OR0, -0(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2- ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -0(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -CN, -NR'C02R°, -NR'NR'C(0)R°, -N(R')C(0)N(R')2, -NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(O)C(0)R°, -C(O)CH2C(O)R0, -C02R°, -C(0)R°, -OC(0)R°, -OC(O)N(R0)2, -S(0)2R°, -S02N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R°, -V-OH, -V-OR0, -V-SH, -V-SR0, -NR'C(O)R°, - V-CN, -V-NR'C02R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°, -V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-CO2R°, -V-C(0)R°, -V-OC(0)R°, -V-OC(O)N(R0)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, -V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, or -V-C(=NH)-N(R')2. Additionally, -N02, -N(R')2, -C(0)N(R°)2, -NR'C(0)R°,
-C(0)N(R°)2, -V-NO2, -V-N(R')2, -V-C(0)N(R°)2, -V-NR'C(0)R° and -V-C(0)N(R°)2 are permissibly values for R10 and Rn and COOR° is a permissible substituent for the substitutable carbon atoms of an aromatic group represented by R1 and R4 and Rings A and B and for other aromatic groups, aliphatic groups and non-aromatic rings that form part(s) of the disclosed CCR8 inhibitors. Other examples of suitable substituents on the saturated carbon of an aliphatic group (including aliphatic groups represented by R4) and a non-aromatic heterocycle include: =0, =S, =NNHR*, =NN(R*)2, =NNHC(0)R*, =NNHCO2(alkyl), =NNHS02 (alkyl), or =NR*. Except as otherwise provided, preferred substituents for aromatic groups, aliphatic groups and non-aromatic rings (including cycloaliphatic rings and non-aromatic heterocyclic rings) that form part(s) of the disclosed CCR8 inhibitors are haloalkyl, alkyl, halogen, cyano, nitro, hydroxy, haloalkoxy and alkoxy. Amine, alkylamine and dialkyamine are also a preferred substituents for substitutable carbon atoms of an aliphatic group or a non-aromatic ring of the disclosed CCR8 inhibitors. A substitutable methylene group in an aliphatic or non- aromatic ring permissably has up to two substituents. Most commonly, however, the carbon atoms of aliphatic groups and non-aromatic rings (e.g., a non-aromatic ring represented by R1, a non-aromatic heterocyclic group formed from NR5(CHm)R1, a non- aromatic ring formed from NR3R4 or a non-aromatic ring represented by R4) of the disclosed CCR8 inhibitors are unsubstituted or substituted with an alkyl group, hydroxyalkyl group or halogen. Each R* is independently selected from hydrogen, an unsubstituted aliphatic group or a substituted aliphatic group, preferably from hydrogen or an alkyl group.
Each R° is independently hydrogen or substituted or unsubstituted aliphatic group, a substituted or unsubstituted cycloaliphatic group, a substituted or unsubstituted non- aromatic heterocyclic group or a substituted or unsubstituted aromatic group, preferably phenyl group. Preferably, each R° is independently hydrogen, an alkyl group, a cycloalkyl group, a non-aromatic heterocyclic group or an aromatic group (preferably phenyl). Each R' is independently R°, -C02R°, -S02R° or -C(0)R°. V is a C1-C6 alkylene group. Suitable substituents on the nitrogen of a non-aromatic heterocyclic group include -R+, -N(R+)2, -C(0)R+, -C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02
N(R+)2, -C(=S)N(R+)2, -C(=NH)-N(R+)2, and -NR+ S02 R+. Other examples include -C(0)-NHR+, -C(0)-N(R+)2, -C(0)-CH[N(R+)2]R+ and -C(O)-CH[OR+]R+ .
Each R+ is independently hydrogen, an aliphatic group, a substituted aliphatic group, phenyl, substituted phenyl, -benzyl, substituted benzyl or an unsubstituted heteroaryl or non-aromatic heterocyclic ring. R+ can also be a substituted non-aromatic heterocyclic group and a substituted or unsubstituted cycloaliphatic group; or N(R+)2 is a non-aromatic heterocyclic group.
Examples of substituents on the aliphatic group represented by R , examples of substituents on the aliphatic, aromatic, cycloaliphatic or non-aromatic heterocyclic group represented by R° and examples of substituents on the aliphatic group, phenyl group or benzyl group represented by R+ include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
An "electron donating group" is a substituent which results in a phenyl ring that has more electron density when the group is present than when it is absent. Electron donating groups have a Hammet sigma value greater than one (see, for example , C. Hansch, A. Leo and D. Hoeckman, "Exploring QSAR Hydrophobic, Electronic and Steric Constants", American Chemical Society (1995), pages 217-32). Examples of electron donating groups include hydroxy, alkoxy, alkyl, alkylamine dialkylamine and amine. Additionally, pharmaceutically acceptable salts of the compounds disclosed herein are also included in the present invention and can be used in the compositions and methods disclosed herein. For example, an acid salt of a compound containing an amine or other basic group can be obtained, by reacting the compound with a suitable organic or inorganic acid, such as hydrogen chloride, hydrogen bromide, acetic acid, perchloric acid and the like. Compounds with a quaternary ammonium group also contain a counteranion such as chloride, bromide, iodide, acetate, perchlorate and the like. Other examples of such salts include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, tartrates [e.g. (+)- tartrates, (-)-tartrates or mixtures thereof including racemic mixtures], succinates, benzoates and salts with amino acids such as glutamic acid. Salts of compounds containing a carboxylic acid or other acidic functional group can be prepared by reacting with a suitable base. Such a pharmaceutically acceptable salt may be made with a base which affords a pharmaceutically acceptable cation, which includes alkali metal salts (especially sodium and potassium), alkaline earth metal salts (especially calcium and magnesium), aluminum salts and ammonium salts, as well as salts made from physiologically acceptable organic bases such as trimethylamine, triethylamine, morpholine, pyridine, piperidine, picoline, dicyclohexylamine, N,N'- dibenzylethylenediamine, 2-hydroxyethylamine, bis-(2-hydroxyethyl)amine, tri-(2- hydroxyethyι)amine, procaine, dibenzylpiperidine, dehydroabietylamine, N,N'- bisdehydroabietylamine, glucamine, N-methylglucamine, collidine, quinine, quinoline, and basic amino acid such as lysine and arginine.
Some of the disclosed CCR8 inhibitors contain one or more chiral centers. The presence of chiral centers in a molecule gives rise to stereoisomers. For example, a pair of optical isomers, referred to as "enantiomers", exist for every chiral center in a molecule; and a pair of diastereomers exist for every chiral center in a compound having two or more chiral centers.
It is to be understood that, when a disclosed CCR8 inhibitor has at least one chiral center, the present invention encompasses one enantiomer of inhibitor free from the corresponding optical isomer, racemic mixture of the inhibitor and mixtures enriched in one enantiomer relative to its corresponding optical isomer. When a mixture is enriched in one enantiomer relative to its optical isomers, the mixture contains, for example, an enantiomeric excess of at least 50%, 75%, 90%, 95% 99% or 99.5%.
The enantiomers of the present invention may be resolved by methods known to those skilled in the art, for example by formation of diastereoisomeric salts which may be separated, for example, by crystallization; formation of diastereoisomeric derivatives or complexes which may be separated, for example, by crystallization, gas-liquid or liquid chromatography; selective reaction of one enantiomer with an enantiomer-specific reagent, for example enzymatic esterification; or gas-liquid or liquid chromatography in a chiral environment, for example on a chiral support for example silica with a bound chiral ligand or in the presence of a chiral solvent. Where the desired enantiomer is converted into another chemical entity by one of the separation procedures described above, a further step is required to liberate the desired enantiomeric form. Alternatively, specific enantiomers may be synthesized by asymmetric synthesis using optically active reagents, substrates, catalysts or solvents, or by converting one enantiomer into the other by asymmetric transformation. When a disclosed CCR8 inhibitor has at least two chiral centers, the present invention encompasses a diastereomer free of other diastereomers, a pair of diastereomers free from other diasteromeric pairs, mixtures of diasteromers, mixtures of diasteromeric pairs, mixtures of diasteromers in which one diastereomer is enriched relative to the other diastereomer(s) and mixtures of diasteromeric pairs in which one diastereomeric pair is enriched relative to the other diastereomeric pair(s). When a mixture is enriched in one diastereomer or diastereomeric pair(s) relative to the other diastereomers or diastereomeric pair(s), the mixture enriched with the depicted or referenced diastereomer or diastereomeric pair(s) relative to other diastereomers or diastereomeric pair(s), for example, by a molar excess of at least 50%, 75%, 90%, 95% 99% or 99.5%. The diastereoisomeric pairs may be separated by methods known to those skilled in the art, for example chromatography or crystallization and the individual enantiomers within each pair may be separated as described above. Specific procedures for chromatographically separating diastereomeric pairs of precursors used in the preparation of compounds disclosed herein are provided in Example 1. In certain instances compounds of the present invention may associated in isolated form with solvent or water, as in a "solvate" or "hydrate". References to the disclosed compounds or structural formulas depicting the disclosed compounds are meant to include such solvates and hydrates.
The disclosed compounds, pharmaceutical compositions and methods can be used to inhibit CCR8 activity, to inhibit 1-309 activity and to inhibit or treat (therapeutically or prophylactically) conditions mediated by CCR8 and/or 1-309, including inflammatory disorders and allergic conditions. The disclosed compounds can also be advantageously used to inhibit conditions mediated by esinophils and monocytes, T lymphocytes and other immune system cells which express CCR8, including inflammatory disorders and allergic mediated by these cells.
Examples of allergic conditions for which the disclosed compounds, pharmaceutical compositions and methods are particularly effective include asthma. Other allergic conditions which are expected to be treatable by inhibiting CCR8 activity include, atopic dermatitis, allergic rhinitis, systemic anaphylaxis or hypersensitivity responses, drug allergies (e.g., to penicillin, cephalosporins), insect sting allergies and dermatoses such as dermatitis, eczema, atopic dermatitis, allergic contact dermatitis and urticaria.
Examples of diseases with an inflammatory component for which the disclosed compounds, pharmaceutical composition and methods are effective include rheumatoid arthritis, osteoarthritis, inflammatory bowel disease [e.g., such as ulcerative colitis, Crohn's disease, ileitis, Celiac disease, nontropical Sprue, enteritis, enteropathy associated with serorlegative arthropathies, microscopic or collagenous colitis, eosinophilic gastroenteritis, or pouchitis resulting after proctocolectomy, and ileoanal anastomosis] and disorders of the skin [e.g., psoriasis, erythema, pruritis, and acne].
Many autoimmune diseases also have an inflammatory component. Examples include multiple sclerosis, systemic lupus erythematosus, myasthenia gravis, juvenile onset diabetes, glomerulonephritis and other nephritides, autoimmune thyroiditis, Behcet's disease and graft rejection (including allograft rejection or graft-versus-host disease). The inflammatory component of these disorders is believed to be mediated, at least in part, by CCR8. Diseases characterized by repurfusion have an inflammatory component that is believed to be mediated, at least in part by CCR8. Examples include stroke, cardiac ischemia, and the like. The disclosed compounds and compositions also can be used to treat these disorders.
Other diseases and conditions with an inflammatory component believed to be mediated by CCR8 include mastitis (mammary gland), vaginitis, cholecystitis, cholangitis or pericholangitis (bile duct and surrounding tissue of the liver), chronic bronchitis, chronic sinusitis, chronic inflammatory diseases of the lung which result in interstitial fibrosis, such as interstitial lung diseases (ILD) (e.g., idiopathic pulmonary fibrosis, or ILD associated with rheumatoid arthritis, or other autoimmune conditions), hypersensitivity pneumonitis, collagen diseases and sarcoidosis. Yet other diseases or conditions with inflammatory components which are amendable to treatment according to methods disclosed herein include vasculitis (e.g., necrotizing, cutaneous, and hypersensitivity vasculitis), spondyloarthropathies, scleroderma, atherosclerosis, restenosis and myositis (including polymyositis, dermatomyositis), pancreatitis and insulin-dependent diabetes mellitus. A subject with a condition having one or more symptoms mediated by CCR8, including one of the aforementioned diseases or conditions, is said "to be in need of CCR8 inhibition". The subject with a disease or condition of this type is "treated" when at least one of the symptoms associated with the disease or condition is alleviated (therapeutic treatment) or inhibited or prevented (prophylactic treatment), in whole or in part.
A "subject" is a mammal, preferably a human, but can also be an animal in need of veterinary treatment, e.g., companion animals (e.g., dogs, cats, and the like), farm animals (e.g., cows, sheep, pigs, horses, and the like) and laboratory animals (e.g., rats, mice, guinea pigs, and the like). As noted above, a "subject in need of CCR8 inhibition" is a subject in whom a beneficial therapeutic or prophylactic effect can be achieved by inhibiting CCR8 function or activity.
An "effective amount" of the disclosed CCR8 inhibitors is the quantity which inhibits CCR8 activity in a subject in need of such inhibition, or which, when administered to a subject with a CCR8 mediated condition or disease, ameliorates the symptoms of the disease, delays the onset of the symptoms and/or increases longevity.
The precise amount of CCR8 inhibitor administered to the subject will depend on the type and severity of the disease or condition and on the characteristics of the subject, such as general health, age, sex, body weight and tolerance to drugs. The dosage may also vary according to the route of administration, which includes oral, aerosol, rectal, transdermal, subcutaneous, intravenous, intramuscular, intraperitoneal and intranasal.
The skilled artisan will be able to determine appropriate dosages depending on these and other factors. An "effective amount" typically ranges between about 0.01 mg/kg/day to about 100 mg/kg/day, preferably between about 0.5 mg/kg/day to about 50 mg/kg/day. The CCR8 inhibitors described herein, and the pharmaceutically acceptable salts thereof can be used in pharmaceutical preparations in combination with a pharmaceutically acceptable carrier or diluent. Suitable pharmaceutically acceptable carriers include inert solid fillers or diluents and sterile aqueous or organic solutions. The CCR8 inhibitor will be present in such pharmaceutical compositions in amounts sufficient to provide the desired dosage amount in the range described herein. Techniques for formulation and administration of the compounds of the instant invention can be found in Remington: the Science and Practice of Pharmacy, 19th edition, Mack Publishing Co., Easton, PA (1995).
For oral administration, the CCR8 inhibitor or salts thereof can be combined with a suitable solid or liquid carrier or diluent to form capsules, tablets, pills, powders, syrups, solutions, suspensions and the like. The tablets, pills, capsules, and the like contain from about 1 to about 99 weight percent of the active ingredient and a binder such as gum tragacanth, acacias, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid, a lubricant such as magnesium stearate; and a sweetening agent such as sucrose lactose or saccharin. When a dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier such as a fatty oil.
Various other materials may be present as coatings or to modify the physical form of the dosage unit. For instance, tablets may be coated with shellac, sugar or both. A syrup or elixir may contain, in addition to the active ingredient, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and a flavoring such as cherry or orange flavor.
For parental administration, the disclosed CCR8 inhibitor, or salts thereof can be combined with sterile aqueous or organic media to form injectable solutions or suspensions. For example, solutions in sesame or peanut oil, aqueous propylene glycol and the like can be used, as well as aqueous solutions of water-soluble pharmaceutically- acceptable salts of the compounds. Dispersions can also be prepared in glycerol, liquid polyethylene glycols and mixtures thereof in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms. In addition, to the formulations described previously, the compounds may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation, for example, subcutaneously or intramuscularly or by intramuscular injection. Thus, for example, as an emulsion in an acceptable oil, or ion exchange resins, or as sparingly soluble derivatives, for example, as sparingly soluble salts.
In accordance with conventional methods for showing structural formulas of compounds, a terminal methyl group in a compound described herein can be shown as a straight line with or without "CH3" on its terminus:
$ or CH3
hi certain aspects, the present invention is directed to a compound represented by Structural Formulas (I), (TT) or (ITT) (and methods of use thereof), provided that when R1 is pyridyl and R4 is a phenyl group, then the phenyl group represented by R4 is substituted with a group other than -NO2, -NRXRX, -CONRxRx, -NRxCORx, or an aliphatic group substituted with -NO2, -NRxRx, -CONRxRx or -NRxCORx. Each Rx is independently H, an aliphatic group, a substituted aliphatic group, an aryl group a substituted aryl group, a non-aromatic ring or a substituted non-aromatic ring. Alternatively, or in addition, the subject matter encompassed by Structural Formlas (I)-(IH) excludes N-[4-[[(4- methoxyphenyl)amino] sulfonyl] - 1 -naphthalenyl] -benzamide, N-[4-[(2-propenylamino)sulfonyl]-l-naphthalenyl]-benzamide, N-[4-(4-morpholinylsulfonyl)-l-naphthalenyl]-benzamide or N-[4-( 1 -piperidinylsulfonyl)- 1 -naphthalenyl] -benzamide . The invention is illustrated by the following examples which are not intended to be limiting in any way.
EXEMPLIFICATION
EXPERIMENTAL PROCEDURE FOR NAPHTHALENE SULFONAMIDES
General
All reactions involving air-sensitive reagents were performed under a nitrogen atmosphere. Reagents were used as received from commercial suppliers unless otherwise noted. Anhydrous solvents such as dimethylformamide (DMF), tetrahydrofuran (THF), dichloromethane (CH2C12), and dioxane were obtained from Aldrich Chemical Company in Sure/Seal bottles. 1H NMR data were recorded using the Bruker UltraShield 300 MHz/54mm instrument equipped with Bruker B-ACS60 Auto Sampler or the Varian 300 MHz instrument. Chemical shifts are expressed in ppm downfield from internal tetramethylsilane. Significant 1H NMR data are reported in the following order: ppm, multiplicity (s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; quin, quintet), and number of protons. Intermediates and final compounds were purified by flash chromatography using one of the following instruments: 1. Biotage 4-channel Quad UV Flash Collector equipped with a Quad 1 Pump Module and the Quad 12/25 Cartridge module. 2. Biotage 12-channel Quad UV Flash Collector equipped with a Quad 3 Pump Module and a Quad 3 Cartridge module. 3. Flash column comb i-flash chromatography instrument. LC/MS spectra were obtained using a MicroMass Platform LC (Phenomenx C18 column, 5 micron, 50 x 4.6 mm) equipped with a Gilson 215 Liquid Handler. Standard LC/MS conditions are as follows: Formic acid-Standard conditions:
Figure imgf000026_0001
LC-MS data were acquired using the "Formic acid-Standard" method unless otherwise noted.
Scheme 1: Preparation of amine intermediates
Figure imgf000027_0001
7
Figure imgf000028_0001
l-Benzyl-3-methyl-piperidin-4-ylamine (1)
To a solution of l-benzyl-3-methyl-piperidin-4-one (2.04 g, 10 mmol) in EtOH (20 mL), was added pyridine (20 mL, 0.25 mol) and hydroxylamine hydrochloride (0.70 g, 10 mmol). After being stirred at 90 °C overnight, the resultant solution was concentrated in vacuo to give the crude product l-benzyl-3-methyl-piperidin-4-one oxime. LCMS m/z: 219 (M + H)+. This material was used without further purification.
To a 25 °C solution of l-benzyl-3-methyl-piperidin-4-one oxime in anhydrous THF (20 mL) was added LAH (1.0 M solution THF), (15 mL, 15 mmol). After being stirred at 50 °C overnight, the resultant mixture was quenched with 20% KOH solution. The aqueous layer was extracted with CH C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude mixture ((±)-cis : (±)-trans = 1:1) 1-benzyl- 3-methyl-piperidin-4-ylamine (1). LCMS m/z: 205 (M + H)+. This material was used without further purification.
Figure imgf000028_0002
(±)-l-BenzyI-3,3-dimethyl-piperidin-4-one (2)
To a solution of l-benzyl-3-methyl-piperidin-4-one (7.0 g, 34 mmol) and Mel (2.4 mL) in THF (100 mL) was added NaOt-Bu (4.2 g, 44 mmol) at 0 °C. The reaction was slowly allowed to warm to room temperature and stirred overnight. The aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product. Flash column chromatography (Hexane/EtOAc, gradient) of the residue gave l-benzyl-3,3-dimethyl-piperidin-4-one, which was converted into l-benzyl-3,3-dimethyl-piperidin-4-ylamine (2) using the same procedure as in Scheme 1-1. LCMS m/z : 220 (M + H)+. This material was used without further purification.
Figure imgf000029_0001
l-Benzyl-3-ethyl-piperidin-4-one (3)
To a -78 °C solution of l-benzyl-piperidin-4-one (3.79 g, 20 mmol) in anhydrous THF (20 mL) was added lithium hexamethyldisilazide (21 mL, 21 mmol of a 1.0 M solution in THF). After being stirred at -78 °C for 30 min, a solution of iodoethane (1.7 mL, 21 mmol) in THF (5 mL) was added to the reaction mixture. The resultant solution was stirred at 25°C for 2h and quenched with water. The aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by flash column chromatography (hexane/EtOAc) to provide 0.51 g (11.5% yield) of l-benzyl-3-ethyl-piperidin-4- one, which was converted into l-benzyl-3-ethyl-piperidin-4-ylamine (3) using the same procedure as in Scheme 1-1. ((±)-cis : (±)-trans = 1:1) LCMS m/z : 219 (M + H)+. This material was used without further purification.
Figure imgf000029_0002
cω-3-Amino-8-aza-bicycIo[3.2.1]octane-8-carboxylic acid ethyl ester (4)
The titled compound was made following the procedure in Scheme 1-1. The oxime (prepared as detailed in Scheme 1-1) (2.5 g) was dissolved in MeOH (10 mL) and AcOH (2 mL) and Pt02 (100 mg) were added at the resultant mixture stirred at room temperature. The reaction mixture was shaken for 2 days at 60 psi under an atmosphere of H2. The resultant solution was filtered and concentrated to give the crude product of racemic 3-amino-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid ethyl ester. It was used without further purification.
Figure imgf000030_0001
l-Benzyl-3,5-dimethyI-piperidin-4-ylamine (5)
To a -78 °C solution of l-benzyl-3-methyl-piperidin-4-one (4.06 g, 20 mmol) in anhydrous THF (20 mL) was added lithium hexamethyldisilazide (21 mL, 21 mmol of a 1.0 M solution THF). After being stirred at -78 °C for 30 min, a solution of iodomethane (1.31 mL, 21 mmol) in THF (5 mL) was added into the reaction mixture. The resultant solution was stirred at 25 °C for 2h and quenched with water. The aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by flash column chromatography (hexane/EtOAc) to provide 1.37 g (31.5% yield) of 1- benzyl-3,5-dimethyl-piperidin-4-one.
Following the same procedure as in Scheme 1-1, the crude product 1 -benzy 1-3,5 - dimethyl-piperidin-4-ylamine (5) was prepared as a mixture of diastereomers. LCMS m/z: 219 (M + H)+. This material was used without further purification.
Figure imgf000030_0002
4-Amino-l-benzyl-piperidine-3-carboxylic acid methyl ester (6)
To a 25 °C solution of l-benzyl-4-oxo-piperidine-3-carboxylic acid methyl ester hydrochloride (2.97 g, 10 mmol) in MeOH (10 mL) was added MP-Carbonate (12 g,
30 mmol, 2.54 mmol/g). After shaking at 25 °C for lh, the solution was filtered. To the resultant solution was added ammonium acetate (7.71 g, 100 mmol). After stirring at 65 °C overnight, sodium cyanoborohydride (610 mg, 10 mmol) was added into the resultant mixture and the mixture further stirred for 2h at 50 °C. The solution was then concentrated in vacuo to give a solid. The resultant solid was dissolved in water (100 mL) and the aqueous layer was extracted with CH C12. The organic extracts were combmed, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product 4-amino-l- benzyl-piperidine-3-carboxylic acid methyl ester (6) as a mixture of diastereomers. LCMS showed m/z: 249 (M + H)+. This material was used without further purification.
Figure imgf000031_0001
l-4-oxo-piperidine-l-carboxylic acid tert-butyl ester l-Benzyl-3-methyl-piperidin-4-one (6.5 g, 32.0 mmol) was dissolved in methanol
(30 mL). Di-tert-butyl dicarbonate (10.46 g, 48.0 mmol) was added followed by palladium hydroxide (20%, 100 mg) and the reaction shaken overnight at 55 psi under a hydrogen atmosphere. The reaction was filtered and concentrated in vacuo to give a clear oil. Flash column chromatography (75:25 hexanes/ethyl acetate) afforded the title compound as a white solid. Wt.: 5.5 g (81%). *H NMR (300 MHz, CDC13) δ 4.18 (m, 2H), 3.25 (m, 1H), 2.84 (m, 1H), 2.53 (m, 1H), 2.43 (m, 2H), 1.50 (s, 9H), 1.05 (d, 3H).
Figure imgf000031_0002
(3R, ¥R)-3-methyI-4-(l-(S)-phenyl-ethylamino)-piperidine-l-carboxylic acid tert-butyl ester
(±)-3-Methyl-4-oxo-piperidine-l-carboxylic acid tert-butyl ester (5.4 g, 25.3 mmol) was dissolved in dichloromethane (75 mL). S-(-)-D-Methylbenzylamine (3.1 g, 3.2 mL, 25.3 mmol) was added followed by sodium triacetoxyborohydride (10.7 g, 50.6 mmol). The reaction was stirred at room temperature overnight. LC MS analysis revealed four components, with only one component clearly separated. The reaction was diluted with dichloromethane (150 mL) and extracted water (2x), brine and dried over MgS04. The solution was filtered and concentrated in vacuo to afford a white foam that was purified by flash column chromatography (84.5:15:0.5 dichloromethane:acetonitrile:NH40H) to afford a clear oil. This material was rechromatographed (89.5:10:0.5 dichloromethaneiacetonitrile÷NH-iOH) to afford the title compound as a clear oil. Wt.: 820 mg (10%). *H NMR (300 MHz, CDC13) δ 7.31 (m, 3H), 7.22 (m, 2H), 3.85 (m, 3H), 2.68 (m, IH), 2.46 (m. IH), 2.17 (m, IH), 1.67 (m, IH), 1.40 (s, 9H), 1.30 (d, 3H), 1.08 (m, 2H), 0.97 (d, 3H); LC/MS m/z 319 (M + H)+.
Figure imgf000032_0001
(3S, 4S)-3-methyl-4-(l-(R)-phenyl-ethylamino)-piperidine-l-carboxylic acid tert-butyl ester
(±)-3-Methyl-4-oxo-piperidine-l-carboxylic acid tert-butyl ester (5.4 g, 25.3 mmol) was dissolved in dichloromethane (75 mL). R-(+)-D-Methylbenzylamine (3.1 g, 3.2 mL, 25.3 mmol) was added followed by sodium triacetoxyborohydride (10.7 g, 50.6 mmol). The reaction was stirred overnight at room temperature. LC MS analysis revealed four components, with only one component clearly separated. The reaction was diluted with dichloromethane (150 mL) and extracted twice with water, once with brine and dried over MgS0 . Filtration and concentration in vacuo afforded a white foam that was purified by flash column chromatography (84.5:15:0.5 CH2Cl2:acetonitrile:NH4OH) to afford a clear oil. The material was rechromatographed (89.5:10:0.5 CH2Cl2:acetonitrile:NH4OH) to afford the title compound as a clear oil. Wt: 547 mg (7%). 'H NMR (300 MHz, CDC13) δ 7.31 (m, 3H), 7.22 (m, 2H), 3.85 (m, 3H), 2.68 (m, IH), 2.46 (m. IH), 2.17 (m, IH), 1.67 (m, IH), 1.40 (s, 9H), 1.30 (d, 3H), 1.08 (m, 2H), 0.97 (d, 3H); LC/MS m/z 319 (M + H)+.
Figure imgf000033_0001
(3R, R)-4-amino-3-methyl-piperidine-l-carboxylic acid tert-butyl ester (7)
(3R, ^R)-3-Methyl-4-(l-(S)-phenyl-ethylamino)-piperidine-l-carboxylic acid tert- butyl ester (810 mg, 2.55 mmol) was dissolved in methanol (15 mL). Palladium hydroxide (20%, 100 mg) was added and the mixture was shaken under a hydrogen atmosphere overnight at 55 psi. The reaction was filtered and concentrated in vacuo to give the title compound as a clear oil. Wt.: 500 mg (92%). NMR (300 MHz, CDC13) δ 4.06 (m, IH), 3.96 (m, IH), 2.73 (m, IH), 2.34 (m, 2H), 1.77 (m, IH), 1.43 (s, 9H), 1.27 (m, 2H), 0.94 (d, 3H); LC/MS m/z 215 (M + H)+.
Figure imgf000033_0002
(3S, iS^-4-amino-3-methyl-piperidine-l-carboxyϊic acid tert-butyl ester (single enantiomer, absolute configuration undetermined)
(3S, ^S -3-Methyl-4-(l-(R)-phenyl-ethylamino)-piperidine-l-carboxylic acid tert- butyl ester (510 mg, 1.60 mmol) was dissolved in methanol (15 mL). Palladium hydroxide (20%, 100 mg) was added and the mixture was shaken under a hydrogen atmosphere overnight at 55 psi. The reaction was filtered and concentrated in vacuo to provide the title compound as a clear oil. Wt.: 320 mg (88%). NMR (300 MHz, CDC13) δ 4.06 (m, IH), 3.96 (m, IH), 2.73 (m, IH), 2.34 (m, 2H), 1.77 (m, IH), 1.43 (s, 9H), 1.27 (m, 2H), 0.94 (d, 3H); LC/MS m/z 215 (M + H)+.
Scheme 2
Figure imgf000034_0001
4-Benzoylamino-naphthalene-l-sulfonic acid (8)
To a solution of 4-amino-naphthalene-l-sulfonic acid (2.3 g, 10.0 mmol) in pyridine (15 mL), was added benzoyl chloride (1.4 mL, 12.0 mmol) and the resultant solution was heated at 100 °C and stirred overnight. The solvent was removed in vacuo and the crude material was recrystallized from MeOH (2x) to give the pyridinium salt of 4-benzoylamino-naphthalene-l-sulfonic acid (2.0 g) as a gray colored solid. H NMR (300 MHz, DMSO) δ 8.92 (m, 3H), 8.60 (t, IH), 8.00 (m, 6H), 7.55 (m, 6H); LC/MS m/z 327 (M - H)\
4-Benzoylamino-naphthalene-l-sulfonyl chloride (9)
To a solution of the pyridinium salt of 4-benzoylamino-napthalene-l-sulfonic acid (2.4 g, 5.9 mmol) in DMF (10 mL), was added thionyl chloride (0.6 mL, 8.8 mmol). The resultant solution was stirred at 25 °C for 3 hours. The reaction mixture was quenched by pouring into ice water and filtered to give the title compound (1.8 g) a pale white solid. This material was used without further purification.1H NMR (300 MHz, DMSO) δ 8.88 (d, IH), 8.09 (d, 2H), 7.97 (d, 2H), 7.55 (m, 6H).
Figure imgf000034_0002
N-[4-(3-Methoxy-phenylsulfamoyI)-naphthalen-l-yl]-benzamide (A-l) To a solution of 4-benzoylamino-naphthalene-l-sulfonyl chloride (320 mg, 0.93 mmol) in CH2C12 (20 mL) was added triethylamine (0.26 mL, 1.85 mmol) and m- anisidine (137 mg, 1.11 mmol). The resultant solution was stirred at 25 °C overnight. The reaction mixture was quenched with water and extracted with CH2C12. The organic extracts were combined, washed with brine, dried over Na S0 , filtered and concentrated to provide the crude product as yellow viscous oil. HPLC purification of the residue gave the title compound (190 mg) as a pale white solid. 'H NMR (300MHz, DMSO) δ 8.72 (d, IH), 8.26 (d, IH), 8.15 (d, IH), 8.02 (d, 2H), 7.78 (d, IH), 7.60 (m, 5H), 7.00 (t, IH), 6.55 (m, 2H), 6.46 (d, IH), 3.56 (s, 3H); LC/MS m/z 433 (M + H)+.
Figure imgf000035_0001
4-(l,3-Dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonic acid (4- methoxyphenyι)-amide (A-2)
The title compound was made following the general procedure detailed in Scheme 2, , , substituting phthalic anhydride for benzoyl chloride and benzylamine for m- anisidine. 'H NMR (300 MHz, CDC13) δ 8.75 (d, IH), 8.20 (d, IH), 8.02 (m, 2H), 7.87 (m, 2H), 7.66 (m, 3H), 7.42 (d, IH), 6.86 (d, 2H), 6.69 (d, 2H), 3.72 (s, 3H);
LC/MS m/z 459 (M + H)+.
Figure imgf000035_0002
N-(4-BenzylsuIfamoyl-naphthaIen-l-yl)-benzamide (A-3) The title compound was made following the general procedure in Scheme 2, substituting benzylamine for m-anisidine. !H ΝMR (300 MHz, DMSO) δ 8.71 (d, IH), 8.18 (m, 2H), 8.11 (d, 2H), 7.90 (d, IH), 7.60 (m, 5H), 7.40 (m, 5H), 4.05 (s, 2H); LC/MS m/z All (M + H)+.
Figure imgf000035_0003
N-[4-(4-PhenyI-piperazine-l-sulfonyl)-naphthalen-l-yl]-benzamide (A-5) The title compound was made following general procedure in Scheme 2, substituting 1-phenyl-pyrazine for m-anisidine.'H NMR (300MHz, DMSO) δ 8.68 (d, IH), 8.22 (d, IH), 8.05 (d, IH), 7.87 (d, IH), 7.60 (m, 5H), 7.15 (m, 2H), 6.85 (d, 2H), 6.72 (t, IH), 3.17 (m, 4H), 3.11 (m, 4H); LC/MS m/z 472 (M + H)+.
Figure imgf000036_0001
N-(4-Phenylsulfamoyl-naphthalen-l-yl)-benzamide (A-7)
The title compound was made following the general procedure in Scheme 2, substituting aniline for m-anisidine. 1H ΝMR (300MHz, MeOD) δ 8.76 (d, IH), 8.16 (d, IH), 8.05 (d, IH), 7.96 (d, 2H), 7.60 (m, 6H), 7.00 (m, 5H), LC/MS m/z 403 (M + H)+.
Figure imgf000036_0002
N-[4-(4-Methyl-piperazine-l-sulfonyl)-naphthalen-l-yI]-benzamide (A-8)
The title compound was made following general procedure in Scheme 2, substituting 1-methyl-pyrazine for -anisidine. 1H ΝMR (300MHz, MeOD) δ 8.74 (d, IH), 8.37 (d, IH), 8.15 (m, 2H), 8.08 (d, 2H), 7.86 (d, IH), 7.55 (m, 5H), 3.36 (m, 4H), 2.86 (m, 4H), 2.50 (s, 3H); LC/MS m/z 410 (M + H)+.
Figure imgf000036_0003
N-[4-(2-Dimethylamino-ethylsulfamoyl)-naphthalen-l-yl]-benzamide (A-9)
The title compound was made following general procedure in Scheme 2, substituting 2-dimethylamino-ethylamine for rn-anisidine. "HΝMR (300MHz, MeOD) δ 8.74 (d, IH), 8.45 (s, IH), 8.30 (d, IH), 8.22 (d, IH), 8.08 (d, 2H), 7.85 (d, IH), 7.65 (m, 5H), 3.10 (m, 4H), 2.74 (s, 6H); LC/MS m/z 398 (M + H)+.
Figure imgf000037_0001
N-(4-Cyclohexylsulfamoyl-naphthalen-l-yl)-benzamide (A-10)
The title compound was made following general procedure in Scheme 2, substituting cyclohexylamine for m-anisidine. *HΝMR (300MHz, MeOD) δ 8.80 (d, IH), 8.33 (d, IH), 8.20 (d, IH), 8.08 (d, 2H), 7.85 (d, IH), 7.66(m, 5H), 3.05 (br s, IH), 1.60 (m, 3H), 1.48 (m, IH), 1.35 (m, IH), 1.25 (m, 5H); LC/MS m/z 409 (M + H)+.
Figure imgf000037_0002
N-(4-Isopropylsulfamoyl-naphthaIen-l-yl)-benzamide (A-ll)
The title compound was made following general procedure in Scheme 2, substituting isopropylamine for m-anisidine H ΝMR (300MHz, DMSO) δ 8.69 (d, IH), 8.19 (d, 2H), 8.09 (d, 2H), 8.02 (d, 2H), 7.81 (d, IH), 7.60 (m, 5H), 3.07 (m, IH), 0.88 (m, 6H); LC/MS m/z 369 (M + H)+.
Figure imgf000037_0003
N-{4-[(Pyridin-4-ylmethyl)-sulfamoyl]-naphthalen-l-yl}-benzamide (A-13) The title compound was made following general procedure in Scheme 2, substituting 4-aminomethyl pyridine for m-anisidine. *H ΝMR (300MHz, MeOD) δ 8.76 (d, IH), 8.22 (d, 2H), 8.14 (d, IH), 8.09 (d, 2H), 7.74 (d, IH), 7.60 (m, 5H), 7.08 (d, 2H), 4.10 (s, 2H); LC/MS m/z 418 (M + H)+.
Figure imgf000038_0001
N-[4-(Pyridin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (A-14)
The title compound was made following general procedure in Scheme 2, substituting 4-aminopyridine for m-anisidine. 1HΝMR (300MHz, DMSO) δ 8.83 (d, IH), 8.26 (d, IH), 8.08 (m, 3H), 7.93 (d, 2H), 7.75 (d, IH), 7.60 (m, 5H), 6.91 (d, 2H); LC/MS m/z 404 (M + H)+.
Figure imgf000038_0002
N-[4-(Pyridin-3-ylsulfamoyl)-naphthalen-l-yl]-benzamide (A-16) The title compound was made following general procedure in Scheme 2, substituting 3-aminopyridine for m-anisidine. 'H ΝMR (300MHz, DMSO) δ 8.85 (d, IH), 8.34 (d, IH), 8.10 (in, 3H), 7.82 (rn, IH), 7.76 (d, IH), 7.58 (in, 6TT), 7.18 (d, IH), 6.71 (t, IH); LC/MS m/z 404 (M + H)+.
Figure imgf000038_0003
N-[4-(Pyridin-3-ylsulfamoyl)-naphthalen-l-yI]-benzamide (A-17) The title compound was made following the general procedure in Scheme 2, substituting 2-aminopyridine for m-anisidine. 1H ΝMR (300MHz, DMSO) δ 8.76 (d, IH), 8.28 (d, IH), 8.20 (d, IH), 8.10 (d, 2H), 8.06 (d, 2H), 7.65 (m, 6H), 7.41 (d, IH), 7.10 (dd, IH); LC/MS m/z 404 (M + H)+.
Figure imgf000039_0001
4-[4-(l,3-Dioxo-l,3-dihydro-isoindoI-2-yl)-naphthalene-l-suIfonylamino]- piperidine-1-carboxylic acid ethyl ester (A-18)
The title compound was made following the general procedure in Scheme 2, substituting phthalic anhydride for benzoyl chloride, and 4-amino-piperidine-l- carboxylic acid ethyl ester for m-anisidine. H NMR (300 MHz, MeOD) δ 8.71 (d, IH), 8.39 (d, IH), 8.03 (m, 2H), 7.89 (m, 2H), 7.58 (m, 4H), 5.10 (br s, IH), 4.07 (q, 2H), 3.94 (m, 2H), 3.36 (br s, IH), 3.08 (m, IH), 2.78 (m, 2H), 1.75 (m, 2H), 1,33 (m, 2H), 1.21 (t, 3H); LC/MS m/z 508 (M + H)+.
Figure imgf000039_0002
(±)-3,3-Dimethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-suIfonylamino]- piperidine-1-carboxylic acid tert-butyl ester (A-19)
The title compound was made following general procedure in Scheme 2, substituting 2-methyl-benzoyl chloride for benzoyl chloride and 4-amino-3,3-dimethyl- piperidine-1-carboxylic acid tert-butyl ester for m-anisidine.*H NMR (300 MHz, MeOD) δ 8.83 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.93 (d, IH), 7.40 (m, 3H), 3.76 (d, IH), 3.55 (d, IH), 2.97 (m, IH), 2.54 (s, 6H); 1.38 (s, 3H), 1.14 (m, IH), 0.77 (s, 3H), 0.61 (s, 3H); LC/MS m/z 552 (M + H)+.
Figure imgf000039_0003
N-[4-(l-Benzyl-3-methyI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (A-20) The title compounds (~1:1 mixture) were made following general procedure in Scheme 2, substituting 2-methyl-benzoyl chloride for benzoyl chloride and 4-amino- l-benzyl-3-methyl-piperidine for zw-anisidine. LC/MS m/z 528 (M + H)+.
Figure imgf000040_0001
(±)-cw-N-[4-(l-Benzyl-3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (A-21) and (-t)-trans-N-[4-(l-Benzyl-3-methyl-piperidin-4- ylsulfamoyl)-naphthaIen-l-yl]-2-methyl-benzamide (A-23) The title compounds were made following general procedure in Scheme 2, substituting 2-methyl-benzoyl chloride for benzoyl chloride and 4-amino- 1-benzyl- 3-methyl-piperidine for m-anisidine. Flash column chromatography of the mixture gave both title compounds respectively. A-21: 1H ΝMR (300 MHz, CDC13) δ 8.73 (d, IH), 8.35 (m, 2H), 8.11 (s, IH), 7.93 (d, IH), 7.65 (m, 3H), 7.44 (m, IH), 7.33 (d, TTT), 7.23(m, 5H), 4.70 (d, IH), 3.38 (q, 2H), 3.29 (m, IH), 2.58 (s, 3H), 2.25 (br s, 2H), 1.75 (m, IH), 1.48 (m, 2H), 0.97 (d, IH); 0.65 (d, 3H); LC/MS m/z 528 (M + H)+. A-23: *H ΝMR (300 MHz, CDC13) δ 8.70 (d, IH), 8.32 (s, IH), 8.25 (s, 2H), 7.93 (d, IH), 7.60 (m, 3H), 7.40 (m, IH), 7.25 (m, 6H), 4.78 (d, IH), 3.38 (q, 2H), 2.72 (m, 2H), 2.55 (s, 3H), 2.24 (m, IH), 1.86 (m, IH), 1.63 (m, 3H), 1.35 (m, 2H); 0.57 (d, 3H); LC/MS m/z 528 (M + H)+.
Figure imgf000040_0002
4-Methyl-4-[4-(2-methyI-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid isopropyl ester (A-22) The title compound was made following general procedure in Scheme 2, substituting 2-methyl-benzoyl chloride for benzoyl chloride and 4-amino-4-methyl-piperidine-l- carboxylic acid tert-butyl ester for rø-anisidine.1H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.380 (m, 2H), 8.19 (d, IH), 7.95 (d, 2H), 7.68 (m, 3H), 7.44 (m, IH), 7.35 (m, 2H), 4.78 (s, IH), 3.40 (m, 2H), 3.03 (m, 2H), 2.68 (s, 3H), 1.72 (m, 2H), 1.470 (m, 2H), 1.38 (s, 9H), 1.18 (s, 3H); LC/MS m/z 524 (M + H)+.
Figure imgf000041_0001
(±)-Λ?-[4-(l-Benzyl-3,3-dimethyI-piperidin-4-ylsulfamoyl)-naphthaIen-l-yl]-2- methyl-benzamide (A-24)
The title compound was made following general procedure in Scheme 2, substituting 2-methyl-benzoyl chloride for benzoyl chloride and 4-amino-l-benzyl-3,3-dimethyl- piperidine-1-carboxylic acid tert-butyl ester for .w-anisidine. 1H NMR (300 MHz, DMSO) δ 8.77 (d, IH), 8.22 (dd, 2H), 7.91 (d, IH), 7.70 (m, 4H), 7.35 (m, 3H), 7.22 (m, 5H), 3.30 (q, 2H), 2.67 (m, IH), 2.57 (m, IH), 2.47 (s, 3H), 2.25 (d, IH), 1.68 (t, IH), 1.56 (d, IH), 1.47 (m, IH), 1.04 (m, IH); 0.85 (s, 3H), 0.45(s, 3H); LC/MS m/z 542 (M + H)+.
Figure imgf000041_0002
N-[4-(l-Benzyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (A-25)
The title compound was prepared following the general procedure in Scheme 2, substituting 4-amino- 1-benzyl-piperidine for m-anisidine.
Figure imgf000041_0003
N-[4-(4-Ethyl-phenylsulfamoyl)-naphthaIen-l-yl]-benzamide (A-26) The title compound was prepared following the general procedure in Scheme 2, substituting 4-ethyl-phenylamine for m-anisidine. *H NMR (300 MHz, DMSO) δ 8.76 (d, IH), 8.21 (d, IH), 8.16 (d, IH), 8.07 (s, IH), 8.04 (m, IH), 7.78 (d, IH), 7.76 (m, 5H), 6.94 (m, 4H), 2.4 (m, 2H), 1.03 (t, 3H); LC/MS (M + H)+ m/z 431.
Figure imgf000042_0001
2- Methyl-penta-2,4-dienoic acid [4-(4-fluoro-phenylsulfamoyl)-naphthalen-l- yl]-amide (A-27)
The title compound was prepared following the general procedure in Scheme 2, substituting 4-fluoro-phenyl-amine for m-anisidine. *H NMR (300 MHz, DMSO) δ 8.74.(d, IH), 8.18 (m, 3H), 8.06 (d, 2H), 7.67 (m, 7H), 7.0 (m, 4H); LC/MS (M + ϊϊ)+ m/z 421.
Figure imgf000042_0002
benzamide (A-28) The title compound was prepared following the general procedure in Scheme 2, substituting 4-isopropyl-phenylamine for m-anisidine. *H ΝMR (300 MHz, DMSO) δ 8.76 (d, IH), 8.25 (d, IH), 8.18 (d, IH), 8.05 (m, 2H), 7.8 (d, IH), 7.65 (m, 5H), 6.95 (m, 4H), 2.7 (m, IH), 1.05 (d, 6H); LC/MS (M + H)+ m/z 445.
Figure imgf000042_0003
N-[Biphenyl-4-yl sulfamoyl)-naphthaIen-l-yl]-benzamide (A-29)
The title compound was prepared following the general procedure in Scheme 2, substituting biphenyl-4-yl amine for m-anisidine. H ΝMR (300 MHz, DMSO) δ 8.79 (d, IH), 8.31 (d, IH), 8.18 (d, IH), 8.05 (s, IH), 8.03 (s, IH), 7.82 (d, IH), 7.76 (m, IH), 7.6 (m, 8H), 7.36 (t, 2H), 7.26 (m, IH), 7.13 (s, IH), 7.11 (s, IH); LC/MS (M + H)+ m/z 479.
Figure imgf000043_0001
N-[4-(4-Trifluoromethyl-phenylsulfamoyl)-naphthalen-l-yl]-benzamide (A-30)
The title compound was prepared following the general procedure in Scheme 2, substituting 4-trifluoromethyl-phenylamine for m-anisidine. 1H ΝMR (300 MHz, DMSO) δ 8.27 (d, IH), 8.11 (d, IH), 8.08 (s, IH), 8.05 (d, 2H), 7.77 (d, IH), 7.58 (m, 5H), 7.42 (d, TTT), 7.12 (d, 2H); LC/MS (M + H)+ m/z 469.
Figure imgf000043_0002
(A-31)
The title compound was prepared following the general procedure in Scheme 2, substituting l-benzyl-piperidin-4-yl amine for m-anisidine. *H ΝMR (300 MHz, MeOD) δ 8.73 (d, IH), 8.30 (d, IH), 8.18 (d, IH), 8.09 (s, IH), 8.07 (rn, IH), 7.80 (d, IH), 7.65 (rn, 5H), 7.42 (rn, 5H), 4.17 (s, 2H), 3.34 (rn, TTT), 2.92 (in, 2H), 1.86 (d, 3H), 1.64 (rn, TTT); LC/MS (M + H)+ m/z 500.
Figure imgf000043_0003
4-(4-Benzoylamino-naphthalene-l-sulfonylanιino)-piperidine-l-carboxyIic acid ethyl ester (A-34)
The title compound was prepared following the general procedure in Scheme 2, substituting 4-amino-piperidine-l-carboxylic acid ethyl ester for m-anisidine. Η ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, IH), 8.11 (m, IH), 8.09 (m, IH), 8.07 (m, IH), 7.82 (d, IH), 7.65 (m, 5H), 4.03 (m, 2H), 3.82 (m, 2H), 2.78 (m, 2H), 1.56 (m, 2H), 1.28 (m, 2H), 1.19 (t, 3H); LC/MS (M + H)+ m/z 480.
Figure imgf000044_0001
N-(4-Cyclopentysulfamoyl-naphthalen-l-yI)-benzamide (A-35)
The title compound was prepared following the general procedure in Scheme 2, substituting cyclopentylamine for m-anisidine. !H ΝMR (300 MHz, MeOD) δ 8.29 (d, IH), 8.19 (d, IH), 8.10 (m, IH), 8.07 (m, IH), 7.82 (d, IH), 7.65 (m, 5H), 3.51 (m, IH), 1.56 (m, 4H), 1.34 (m, 5H); LC/MS (M + H)+ m/z 395.
Figure imgf000044_0002
3-(4-Benzoylamino-naphthalene-l-suIfonylamino)-pyrroIidine-l-carboxylic acid tert-butyl ester (A-37)
The title compound was prepared following the general procedure in Scheme 2, substituting 3-amino-pyrrolidine-l-carboxylic acid tert-butyl ester for m-anisidine. Η ΝMR (300 MHz, MeOD) δ 8.79 (d, IH), 8.35 (d, IH), 8.25 (d, IH), 8.11 (d, 2H), 7.89 (m, IH), 7.69 (m, 5H), 3.78 (m, IH), 3.03 (m, IH), 1.88 (m, IH), 1.71 (m, IH), 1.41 (d, 9H); LC/MS (M + H)+ m/z 496.
Figure imgf000044_0003
4-(4-Benzoylamino-naphthalene-l-sulfonyIamino)-piperidine-l-carboxylic acid tert-butyl ester (A-38) The title compound was prepared following the general procedure in Scheme 2, substituting 4-amino-piperidine-l-carboxylic acid tert-butyl ester for m-anisidine. *H ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, IH), 8.19 (d, IH), 8.09 (rn, IH), 8.07 (rn, IH), 7.82 (d, IH), 7.65 (rn, 5H), 3.78 (rn, 2H), 2.73 (rn, 2H), 1.52 (rn, 3H), 1.39 (s, 9H), 1.28 (rn, 2H); LC/MS (M + H)+ m/z 510.
Figure imgf000045_0001
4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (A-40) The title compound was prepared following the general procedure in Scheme 2, substituting 4-amino-piperidine-l-carboxylic acid ethyl ester for m-anisidine and 2- rnethyl benzoyl chloride for benzoyl chloride. *H NMR (300 MHz, MeOD) δ 8.74 (d, 1.H), 8.31 (d, IH), 8.23 (d, IH), 7.92 (d, IH), 7.72 (rn, 3H), 7.39 (rn, 3H), 4.04 (q, TTT), 3.83 (rn, TTT), 3.25 (rn, IH), 2.78 (rn, 2H), 2.55 (s, 3H), 1.56 (rn, 2H), 1.28 (rn, 2H), 1.18 (t, 3H); LC/MS (M + H)+ m/z 496.
Figure imgf000045_0002
(3R, ¥R)-3-Methyl-4-[4-(2-methyl-benzoylanιino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid tert-butyl ester (A-41) The title compound was prepared according to the general procedure in Scheme 2, substituting (3R, ¥R)-4-amino-3-methyl-piperidine-l-carboxylic acid tert-butyl ester for m-anisidine, and 2-methylbenzoyl chloride for benzoyl chloride. !H NMR (300 MHz, CDC13) δ8.69 (d, IH), 8.40 (m, IH), 8.32 (m, IH), 8.12 (s, IH), 7.69 (m, IH), 7.63 (m, 2H), 7.43 (m, IH), 7.32 (m, 2H), 4.48 (d, IH), 3.87 (m, 2H), 2.82 (m, IH), 2.57 (s, 3H), 2.28 (m, IH), 1.64 (m, IH), 1.17 (m, 2H), 0.58 (m, 3H); LC/MS m/z 538 (M + H)+.
Figure imgf000046_0001
(3S, 4S)-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyIamino]-piperidine-l-carboxylic acid tert-butyl ester (A-42)
The title compound was prepared according to the general procedure in Scheme 2, substituting (3S, 4S)-4-amino-3-methyl-piperidine-l-carboxylic acid tert-butyl ester for m-anisidine, and 2-methylbenzoyl chloride for benzoyl chloride. !H NMR (300 MHz, CDC13) δ8.69 (d, IH), 8.40 (m, IH), 8.32 (m, IH), 8.12 (s, IH), 7.69 (m, IH), 7.63 (m, TTT), 7.43 (m, IH), 7.32 (m, 2H), 4.48 (d, IH), 3.87 (m, 2H), 2.82 (m, IH), 2.57 (s, 3H), 2.28 (m, IH), 1.64 (m, IH), 1.17 (m, 2H), 0.58 (m, 3H); LC/MS m/z 538 (M + H)+.
Figure imgf000046_0002
4-[4-(2-Chloro-benzoylamino)-naphthalene-l-sulfonylanrino]-piperidine-l- carboxylic acid ethyl ester (A-43) The title compound was made following general procedure in Scheme 2, substituting 4-(2-chloro-benzoylamino)-naphthalene-l-sulfonyl chloride for 4-benzoylamino- naphthalene-1-sulfonyl chloride benzylamine and substituting 4-amino-piperidine-l- carboxylic acid ethyl ester for m-anisidine. *H NMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, TTT), 7.98 (d, 2H), 7.73 (rn, 3H), 7.53 (rn, 3H), 4.02 (q, 2H), 3.72 (d, TTT), 3.42 (rn, IH), 2.75 (rn, 2H), 1.55 (rn, TTT), 1.25 (rn, TTT), 1.15 (t, 3H); LC/MS m/-? 516 (M + H)+
Figure imgf000047_0001
4-[4-(2-Chloro-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (A-44)
The title compound was made following general procedure in Scheme 2, substituting 4-(2-chloro-benzoylamino)-naphthalene-l-sulfonyl chloride for 4-benzoylamino- naphthalene-1-sulfonyl chloride benzylamine and substituting 4-amino-piperidine-l- carboxylic acid tert-butyl ester for m-anisidine. !H NMR (300 MHz, CDC13 ) δ 8.70 (m, 2H), 8.36 (m, 2H), 8.08 (d, IH), 7.90 (m, IH), 7.67 (m, 2H), 7.48 (m, 3H), 4.80 (d, IH), 3.82 (m, 2H), 3.25 (m, IH), 2.70 (t, 2H), 1.65 (m, 3H), 1.35 (s, 9H), 1.20 (m, 2H); LC/MS m/z 544 (M + H)+
Figure imgf000047_0002
(±)-(cis, tr««s)-N-[4-(l-Benzyl-3,5-dimethyl-piperidin-4-yIsulfamoyl)- naphthalen-l-yl]-2-methyl-benzamide (A-45) and (±)-(cis, c s)-N-[4-(l-BenzyI- 3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl-benzamide (A-46)
The title compounds were made following general procedure in Scheme 2, substituting 4-(2-methyl-benzoylamino)-naphthalene-l-sulfonyl chloride for 4- benzoylamino-naphthalene-1-sulfonyl chloride benzylamine and substituting 1- benzyl-3,5-dimethyl-piperidin-4-ylamine 6 for m-anisidine. After flash column separation, A-45 and A-46 were obtained. A-45: JH ΝMR (300 MHz, CDC13) δ 8.77(d, IH), 8.36 (m, 2H), 8.10 (s, IH), 7.92 (d, IH), 7.66 (m, 3H), 7.44 (m, IH),
7.34 (m, IH), 7.22 (m, 6H), 4.65 (d, IH), 3.34 (dd, 2H), 2.90 (m, IH), 2.59 (s, 3H),
2.35 (m, IH), 2.05 (d, IH), 1.70 (s, br, 3H), 1.57 (s, IH), 0.75 (d, 3H), 0.60 (d, 3H); LC/MS m/z 543 (M + H)+ ; A-46: JH ΝMR (300 MHz, CDC13) δ 8.25(d, IH), 8.34 (m, 4H), 7.98 (d, IH), 7.64 (m, 3H), 7.43 (m, IH), 7.31 (m, 6H), 6.15 (d, IH), 3.84 (s, 2H), 3.40 (d, IH), 2.80 (d, 3H), 2.56 (s, 3H), 2.30 (t, 2H), 2.10 (s, br, 2H), 0.42 (d, 6H); LC/MS m/z 543 (M + H)+
Figure imgf000048_0001
(±)-(cw)-l-Benzyl-4-[4-(2-methyl-benzoylamino)-naphthaIene-l-suIfonylamino]- piperidine-3-carboxylic acid ethyl ester (A-47) and (±)-(trfl«5')-l-Benzyl-4-[4-(2- methyl-benzoylamino)-naphthalene-l-suIfonylamino]-piperidine-3-carboxylic acid ethyl ester (A-48) The title compounds were made following general procedure in Scheme 2, substituting 4-(2-methyl-benzoylamino)-naphthalene-l-sulfonyl chloride for 4- benzoylamino-naphthalene-1-sulfonyl chloride benzylamine and substituting 4- amino-l-benzyl-piperidine-3-carboxylic acid ethyl ester 5 for m-anisidine. After flash column separation, A-47 and A-48 were obtained. A-47: *H NMR (300 MHz, CDC13) δ 8.65 (d, IH), 8.32 (m, 2H), 8.30 (s, IH), 7.88 (d, IH), 7.64 (m, 3H), 7.42 (t, IH), 7.32 (m, 2H), 7.20 (m, 5H), 6.18 (d, IH), 3.85 (m, 2H), 3.45 (m, IH), 3.25 (m, 2H), 3.00 (d, IH), 2.65 (s, IH), 2.55 (s, 3H), 2.35 (s, IH), 1.80 (m, 3H), 1.42 (m, IH), 1.00 (t, 3H); LC/MS m/z 586 (M + H)+ ; A-48: Η NMR (300 MHz, CDC13) δ 8.64 (d, IH), 8.36 (m, 2H), 8.10 (s, IH), 7.90 (d, IH), 7.65 (m, 3H), 7.42 (t, IH), 7.32 (m, 2H), 7.24 (m, 5H), 4.95 (d, IH), 3.50 (m, 4H), 2.86 (d, IH), 2.70 (m, 2H), 2.51 (s, 3H), 2.20 (t, IH), 2.02 (t, IH), 1.88 (m, 3H), 1.48 (m, IH), 1.00 (t, 3H); LC/MS m/z 586 (M + H)+
Figure imgf000048_0002
(±)-(cώ)-N-[4-(l-Benzyl-3-ethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (A-49) and (±)-(trans)-N-[4-(l-Benzyl-3-ethyl-piperidin-4- ylsulfamoyl)-naphthalen- 1 -yl] -2-methyl-benzamide (A-50) The title compounds were made following general procedure in Scheme 2, substituting 4-(2-methyl-benzoylamino)-naphthalene-l-sulfonyl chloride for 4- benzoylamino-naphthalene-1-sulfonyl chloride benzylamine and substituting 1- benzyl-3-ethyl-piperidin-4-ylamine 3 for m-anisidine. After flash column separation and further HPLC purification, A-49 and A-50 formic acid salts were obtained. A- 49: *H ΝMR (300 MHz, CDC13) 8.42 (d, IH), 8.18 (s, IH), 8.00 (d, 2H), 7.65 (d, IH), 7.30 (m, 3H), 7.05 (t, IH), 6.95 (m, 8H), 5.30 (s, br, IH), 3.50 (s, br, IH), 3.20 (q, 2H), 3.08 (s, IH), 2.21 (s, 3H), 2.05 (m, 3H), 1.20 (m, 3H), 0.60 (m, 2H), 0.05 (t, 3H); LC/MS m/z 542 (M + H)+ ; A-50: *H ΝMR (300 MHz, CDC13) δ 8.70 (d, IH), 8.30 (m, 2H), 8.20 (s, IH), 7.90 (d, IH), 7.60 (m, 3H), 7.42 (t, IH), 7.25 (m, 8H), 4.75 (d, IH), 3.45 (dd, 2H), 2.85 (m, 2H), 2.60 (m, IH), 2.55 (s, 3H), 1.85 (t, IH), 1.75 (t, IH), 1.40 (m, 4H), 0.85 (m, IH), 0.55 (t, 3H); LC/MS m/z 542 (M + H)+
Scheme 3
4-Amino-naphthalene-l-suIfonic acid (4-methoxy-phenyl)-amide (10)
To a solution of sulfonamide (A-2) (0.75 g, 1.64 mmol) in methanol (10 mL) was added hydrazine (ImL). The resultant solution was stirred at 55 °C for 2 hr. A precipitate formed which was filtered and washed with a small amount of methanol. The filtrate was collected and solvent was removed in vacuo to give the title compound as white solid (0.7 g). !H NMR (300 MHz, DMSO) δ 9.84 (br s, IH), 8.55 (d, IH), 8.16 (d, IH), 7.80 (d, IH), 7.60 (t, IH), 7.47 (t, IH), 6.82 (d, 2H), 6.71 (m, 3H), 6.53 (d, IH), 3.58 (s, 3H); LC/MS m/z 329 (M + H)+.
Figure imgf000050_0001
4-Methoxy-N-[4-(4-methoxy-phenylsulfamoyl)-naphthalen-l-yl]-benzamide (B-
2)
To a solution of naphthalenyl amine (10) (65 mg, 0.2 mmol) in CH2C12 (5 mL) was added j--methoxybenzoyl chloride (45 uL, 0.24 mmol) and Et3Ν (50 uL, 0.4 mmol). The resultant solution was stirred at 25 °C overnight. The solvent was removed in vacuo and the residue was purified using HPLC to give the title compound (30 mg) as pale yellow solid.. 1HNMR (300MHz, MeOD) δ 8.73 (d, IH), 8.08 (m, 4H), 7.70 (m, 3H), 7.10 (d, 2H), 6.90 (d, TTT), 6.70 (d, 2H), 3.84 (s, 3H), 3.60 (s, 3H); LC/MS m/z 463 (M + H)+.
Figure imgf000050_0002
N-[4-(4-Methoxy-phenyIsulfamoyI)-naphthalen-l-yl]-4-nitro-benzamide (B-3)
The title compound was made following general procedure in scheme 3, substituting / nitrobenzoyl chloride for^-methoxy-benzoyl chloride. 1H ΝMR (300 MFIz, DMSO) δ 8.24 (d, 2H), 8.02 (m, 3H), 7.55 (d, 2H), 7.48 (m, IH), 7.18 (d, 2H), 6.83 (d, 2H), 6.69 (d, IH), 3.69 (s, 3H); LC/MS m/z 478 (M + H)+.
Figure imgf000050_0003
Cyclohexanecarboxylic acid [4-(4-methoxy-phenylsulfamoyι)-naphthalen-l-yl]- amide (B-4) The title compound was made following general procedure in Scheme 3, substituting cyclohexyl carboxyl chloride for -methoxy-benzoyl chloride. !H NMR (300MHz, DMSO) δ 10.28 (s, IH), 10.05 (s, IH), 8.74 (d, IH), 8.25 (d, IH), 8.08 (d, IH), 7.85 (d, IH), 7.70 (m, TTT), 6.86 (d, TTT), 6.67 (d, 2H), 3.60 (s, 3H), 2.60 (m, IH), 1.50 (m, 10H); LC/MS m/z 439 (M + H)+.
Figure imgf000051_0001
3-Methoxy-N-[4-(4-methoxy-phenylsulfamoyl)-naphthalen-l-yl]-benzamide (B-
5) The title compound was made following general procedure in Scheme 3, substituting 3-methoxy-benzoyl chloride for jo-methoxy-benzoyl chloride. 1H ΝMR (300MHz, DMSO) δ 10.67 (s, IH), 10.32 (br s, IH), 8.79 (d, IH), 8.22 (d, IH), 8.19 (s, 2H), 7.90 (d, IH), 7.79 (d, 2H), 7.62 (t, IH), 7.31 (m, IH), 7.18 (t, IH), 6.92 (d, 2H), 6.76 (d, 2H), 3.63 (s, 3H), 3.37 (s, 3H); LC/MS m/z 463 (M + H)+.
Figure imgf000051_0002
2-Methoxy-N-[4-(4-methoxy-phenylsulfamoyl)-naphthalen-l-yl]-benzamide (B-
6)
The title compound was made following general procedure in Scheme 3, substituting 2-methoxy benzoyl chloride for 7-methoxy-benzoyl chloride. *H ΝMR (300MHz, DMSO) δ 10.60 (s, IH), 10.2 (br s, IH), 8.87 (d, IH), 8.40 (d, IH), 8.11 (s, 2H), 7.84 (d, IH), 7.76 (d, 2H), 7.55 (t, IH), 7.45 (d, IH), 7.12 (t, IH), 6.88 (d, 2H), 6.70 (d, 2H), 3.60 (s, 3H), 3.34 (s, 3H); LC/MS m/z 463 (M + H)+.
Figure imgf000052_0001
N-[4-(4-Methoxy-phenylsulfamoyl)-naphthalen-l-yl]-2-phenyl-acetamide (B-7)
The title compound was made following general procedure in Scheme 3, substituting phenylacetyl chloride for 7-methoxy-benzoyl chloride. *H ΝMR (300MHz, DMSO) δ 10.30 (s, IH), 10.18 (s, IH), 8.67 (d, IH), 8.24 (d, IH), 8.05 (s, IH), 7.84 (d, IH), 7.66 (m, 2H), 7.30 (m, 5H), 6.82 (d, 2H), 6.67 (d, 2H), 3.81 (s, TTT), 3.55 (s, 3H), 3.29 (s, 3H); LC/MS m/z 447 (M + H)+.
Figure imgf000052_0002
N-[4-(4-Methoxy-phenylsulfamoyl)-naphthalen-l-yI]-isonicotinamide (B-8)
The title compound was made following general procedure in Scheme 3, substituting isonicotinoyl chloride for / methoxy-benzoyl chloride. !H ΝMR (300MHz, DMSO) δ 8.82 (d, 2H), 8.78 (d, IH), 8.22 (d, IH), 8.17 (d, IH), 7.98 (d, 2H), 7.80 (d, 2H), 7.72 (m, IH), 6.92 (d, 2H), 6.74 (d, TTT), 3.62 (s, 3H); LC/MS m/z 434 (M + H)+.
Figure imgf000052_0003
4-(3-Phenyl-thioureido)-naphthaIene-l-suIfonic acid (4-methoxy-phenyl)-amide (B-9)
The title compound was made following general procedure in Scheme 3, substituting phenyl isothionitrile for /j-methoxy-benzoyl chloride. !H ΝMR (300MHz, DMSO) δ 8.73 (d, IH), 8.10 (d, IH), 8.08 (d, IH), 7.70 (m, 3H), 7.50 (d, 2H), 7.32 (t, 2H), 7.13 (t, IH), 6.90 (d, 2H), 6.70 (d, 2H), 3.60 (s, 3H); LC/MS m/z 464 (M + H)+.
Figure imgf000053_0001
4-(3-Phenyl-ureido)-naphthalene-l-suIfonic acid (4-methoxy-phenyl)-amide (B- 10)
The title compound was made following general procedure in Scheme 3, substituting phenyl isocyanate for / methoxy-benzoyl chloride. *HNMR (300MHz, DMSO) δ 8.58 (d, IH), 8.05 (m, 3H), 7.48 (m, 2H), 7.40 (d, 2H), 7.22 (m, TTT), 6.96 (t, IH), 6.75 (d, 2H), 6.65 (d, 2H), 3.58 (s, 3H); LC/MS m/z 448 (M + H)+.
Figure imgf000053_0002
N-[4-(4-Methoxy-phenyϊsulfamoyl)-naphthalen-l-yl]-2-methyl-benzamide (B-
11)
The title compound was made following general procedure in Scheme 3, substituting o-tolyl chloride for^-methoxy-benzoyl chloride. !H ΝMR (300 MHz, DMSO) δ 8.75 (d, IH), 8.24 (d, IH), 8.14 (d, IH), 7.86 (d, IH), 7.71 (m, 3H), 7.42 (m, IH), 7.36 (m, 2H), 6.90 (d, 2H), 6.70 (d, TTT); 3.60 (s, 3H), 2.45 (s, 3H); LC/MS m/z 447 (M + H)+.
Figure imgf000053_0003
4-[4-(Cyclohexanecarbonyl-amino)-naphthalene-l-suIfonylamino]-piperidine-l- carboxylic acid ethyl ester (B-12)
The title compound was prepared following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid ethyl ester for / anisidine and cyclohexane carbonyl chloride for -methoxy-benzoyl chloride. *H ΝMR (300 MHz, DMSO) δ 10.05 (s, IH), 8.65 (d, IH), 8.26 (d, IH), 8.14 (d, IH), 8.04 (d, IH), 7.92 (d, IH), 7.71 (m, 2H), 3.95 (m, 3H), 3.68 (m, 2H), 1.93 (m, 2H), 1.80 (m, 2H), 1.31 (m, 13H), 1.13 (t, 3H); LC/MS (M + H)+ m/z 488.
Figure imgf000054_0001
4-[4-(3-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (B-13)
The title compound was prepared following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid ethyl ester for/?-anisidine and 3- methyl benzoyl chloride for 7-methoxy-benzoyl chloride. *H NMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.30 (d, IH), 8.18 (d, IH), 7.80 (m, 5H), 7.46 (m, TTT), 4.03 (q, TTT), 3.83 (d, 2H), 3.23 (m, IH), 2.78 (m, 2H), 2.47 (s, 3H), 1.56 (m, 2H), 1.28 (m, 2H), 1.19 (t, 3H); LC/MS (M + H)+ m/z 496.
Figure imgf000054_0002
4-{4-[(Piperidine-l-carbonyl)-amino]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (B-14)
The title compound was prepared following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid ethyl ester for /?-anisidine and 1- piperidine carbonyl chloride for /?-methoxy-benzoyl chloride.
Figure imgf000054_0003
4-[4-(2-Fluoro-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (B-15) The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for jo-anisidine and 2-fluorobenzoyl chloride for 7-methoxy-benzoyl chloride. !H NMR (300 MHz, DMSO) δ 10.72(s, IH), 8.67(d, IH), 8.30(d, IH), 8.20(d, IH), 8.10(d, IH), 8.01(d, IH), 7.83(t, IH), 7.74(t, 2H), 7.65(m, IH), 7.41(q, 2H), 3.67(d, 2H), 3.18(m, IH), 2.70(m, 2H), 1.43(m, 2H), 1.33(s, 9H), δ 1.18(m, TTT). LC/MS m/z 527 (M - H)_, 529 (M + H)+
Figure imgf000055_0001
4-[4-(CyclopentanecarbonyI-aniino)-naphthalene-l-sulfonylamino]-piperidine- l-carboxylic acid tert-butyl ester (B-16)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for/?-anisidine, and cyclopentanecarbonyl chloride for -methoxy-benzoyl chloride. JH NMR (300 MHz, DMSO) δ 10.1 l(s, IH), 8.64(d, IH), 8.25(d, IH), 8.13(d, IH), 8.01(d, IH), 7.92(d, IH), 7.89(m, IH), 7.70(m, 2H), 3.61(d, 2H), 3.11(m, 2H), 1.94(m, 2H), 1.84-1.60 (m, 7H), 1.38(d, 2H), 1.33(s, 9H), 1.12(m, 2H). LC/MS m/z 500 (M - H)", 502 (M + H)+
Figure imgf000055_0002
4-[4-(CyclopropanecarbonyI-amino)-naphthaIene-l-sulfonylamino]-piperidine-
1-carboxylic acid tert-butyl ester (B-17)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for/7-anisidine, and cyclopropanecarbonyl chloride for / methoxy-benzoyl chloride. !H NMR (300 MHz, DMSO) δ 10.43 (s, IH), 8.65 (d, IH), 8.34 (d, IH), 8.12 (d, IH), 7.99(t, 2H), 7.73 (m, 2H), 3.61 (d, 2H), 3.13 (m, TTT), 2.68 (m, 2H), 2.16 (m, 2H), 2.16 (m, IH), 1.39 (d, 2H), 1.33 (s, 9H), 1.12 (m, 2H), 0.88 (d, 4H); LC/MS m/z 472 (M - fff, 474 (M + H)+
Figure imgf000056_0001
4-[4-(Cyclobutanecarbonyl-amino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (B-18)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for j_-anisidine, and cyclobutanecarbonyl chloride fory3-methoxy-benzoyl chloride. *H NMR (300 MHz, DMSO) δ 9.98 (s, IH), 8.62 (d, IH), 8.21 (d, IH), 8.12 (d, IH), 7.99 (d, IH), 7.95 (d, IH), 7.70 (m, 2H), 3.59 (d, 2H), 3.51 (t, IH), 3.13 (m, IH), 2.67 (m, 2H), 2.32-2.16 (m, 4H), 1.99 (m, IH), 1.84 (m, IH), 1.37 (d, 2H), 1.31 (s, 9H), 1.10(m, 2H); LC/MS m/z 486 (M - H)", 488 (M + H)+
Figure imgf000056_0002
4-[4-(Cyclohexanecarbonyl-amino)-naphthalene-l-suIfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (B-19)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester fory^-anisidine and cyclohexanecarbonyl chloride for^»-methoxy-benzoyl chloride. !H NMR (300 MHz, DMSO) δ 10.05 (s, IH), 8.64 (d, IH), 8.25 (d, IH), 8.12 (d, IH), 8.00 (d, IH), 7.91 (d, IH), 7.71 (m, TTT), 3.61 (d, 2H), 3.43 (m, IH), 3.15 (m, IH), 2.65 (m, 2H), 1.90 (d, 2H), 1.77 (d, 2H), 1.69 (m, IH), 1.54-1.33 (m, 5H), 1.32 (s, 9H), 1.30-1.12 (m, 4H); LC/MS m/z 486 (M - H)", 488 (M + H)+
Figure imgf000057_0001
4-{4-[(Pyridine-3-carbonyl)-amino]-naphthalene-l-suIfonylamino}-piperidine- l-carboxylic acid tert-butyl ester (B-20)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for 7-anisidine, and nicotinoyl chloride hydrochloride for jo-methoxy-benzoyl chloride. *H NMR (300 MHz, DMSO) δ 10.83 (s, IH), 9.23 (d, IH), 8.81 (d, IH), 8.67 (dd, IH), 8.11 (dt, IH), 8.27 (dd,l H), 8.27 (dd, IH), 8.20 (d, IH), 8.09 (d, IH), 7.85 (d, IH), 7.75 (m, 2H), 7.6 (m, IH), 3.62 (d, 2H), 3.18 (m, IH), 2.69 (m, 2H), 1.45-1.37 (m, 2H), 1.30 (s, 9H), 1.14 (m, 2H); LC/MS m/z 509 (M - HT, 511 (M + H)+
Figure imgf000057_0002
4-{4-[(l-MethyI-piperidine-4-carbonyl)-amino]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid tert-butyl ester (B-21)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for / anisidine, N- methyl-piperdine-4-carboxylic acid hydrochloride for /p-methoxy-benzoyl chloride and reagents l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI), 1-hydroxybenzotriazole hydrate (HOBt) and pyridine for dimethylamino pyridine (DMAP) and triethylamine. 1H ΝMR (300 MHz, DMSO) δ 10.39 (s, IH), 8.64 (dd, IH), 8.29 (dd, IH), 8.14 (d, IH), 8.05 (d, IH), 7.89 (d, IH), 7.72 (m, 2H), 3.62 (d, 2H), 3.40 (m, 2H), 3.15 (m, IH), 2.95 (m, 2H), 2.78-2.67 (m, 6H), 2.09 (m, 2H), 2.0 (m, 2H), 1.84 (m, IH), 1.39 (m, IH), 1.32 (s, 9H), 1.18 (m, 2H); LC/MS m/z 484 (M - H)\ 486 (M + H)+
Figure imgf000058_0001
4-{4-[(Pyridine-4-carbonyl)-amino]-naphthalene-l-sulfonylamino}-piperidine- 1-carboxylic acid tert-butyl ester (B-22)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for ?-anisidine and isonicotinoylchloride hydrochloride for 7-methoxy-benzoyl chloride. LC/MS m/z 511 (M + H)+
Figure imgf000058_0002
4-{4-[(l-Methyl-piperidine-3-carbonyl)-amino]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid tert-butyl ester (B-23)
The title compound was made following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for 7-anisidine, N- methyl-piperidine-3 -carbonyl chloride (prepared in situ from N-methyl-piperidine-3- carboxylic acid, oxalyl chloride (1.2eq) and triethylamine (1 eq)) for / methoxy- benzoyl chloride. LC/MS m/z 531 (M + H)+
Figure imgf000058_0003
4-{4-[(2-Methyl-pyridine-3-carbonyl)-amino]-naphthalene-l-sulfonylamino}- piperidine-l-carboxylic acid ethyl ester (B-24):
To a suspension of 4-(4-Amino-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid ethyl ester (0.26 g, 0.71 mmol) (prepared following the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid ethyl ester for/7-anisidine) in CH2C12 (10 mL) and aqueous saturated sodium bicarbonate solution (4 mL) was added 2-methyl nicotinic chloride (0.16 g, 1.07 mmol) and the resulting mixture was stirred at room temperature overnight. The organic layer was separated, dried over sodium sulfate and concentrated. Purification of the residue by column chromatography (2-5% MeOH/CH2Cl2) provided the B-24 (0.09g, 26%). 'H NMR (300MHz, CDC13) δ 8.61-8.66 (m, 2H), 8.34 (s, IH), 8.19-8.28 (m, IH), 7.94 (d, 2H), 7.60-7.70 (m, 2H), 7.28-7.3 l(m, IH), 4.91(d, IH), 4.03 (q, 2H), 3.85 (d, TTT), 3.20-3.32 (m, IH), 2.80 (s, 2H), 2.63-2.74 (m, TTT), 1.67 (br s, 4H), 1.16- 1.21 (m, 5H). LC/MS m/z 497 (M + H)+.
Figure imgf000059_0001
4-[4-(2-Cyano-benzoylamino)-naphthalene-l-suIfonylamino]-piperidine-l- carboxylic acid ethyl ester (B-26) A solution of 2-cyano-benzoic acid (294 mg, 2 mmol) in thionyl chloride (5 mL) was heated to reflux where the mixture was stirred for 3 h and then concentrated in vacuo. The crude material, 2-cyano-benzoyl chloride was used without purification. The title compound was made following the general procedure in scheme 3, substituting 4-(4-amino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid ethyl ester for 4-amino-naphthalene-l-sulfonic acid (4-methoxy-phenyl)-amide and substituting 2-cyano-benzoyl chloride for -methoxy-benzoyl chloride. ^NMR (300 MHz, MeOD) δ 8.05 (dd, IH), 8.36 (d, IH), 8.05 (m, 2H), 7.92 (m, 2H), 7.83 (m, IH), 7.75 (m, IH), 7.64 (d, 2H), 6.89 (td, IH), 4.05 (q, 2H), 3.85 (d, 2H), 3.30 (m, IH), 2.80 (m, 2H), 1.60 (m, 2H), 1.30 (m, 2H), 1.20 (t, 3H); LC/MS m/z 508 (M + H)+
Figure imgf000060_0001
4-[4-[4-(2,3-Dimethyl-benzoylamino)-naphthaIene-l-sulfonylamino]-piperidine- 1-carboxylic acid ethyl ester (B-27)
The title compound was made following general procedure in Scheme 3, substituting 4-(4-amino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid ethyl ester for 4-amino-naphthalene-l-sulfonic acid (4-methoxy-phenyl)-amide and substituting 2,3-dimethyl-benzoyl chloride for j methoxy-benzoyl chloride. 'H NMR (300 MHz, MeOD/CDCl3) δ 8.63 (d, IH), 8.24 (m, 2H), 7.97 (d, IH), 7.60 (m, 2H), 7.38 (m, IH), 7.30 (m, 2H), 4.00 (q, 2H), 3.81 (d, TTT), 3.20 (m, IH), 2.75 (m, 2H), 2.40 (s, 3H), 2.30 (s, 3H), 1.58 (m, 2H), 1.20 (m, 2H), 1.12 (t, 3H); LC/MS m/z 510 (M + H)+
Figure imgf000060_0002
4-[4-(2,5-Dimethyl-benzoylamino)-naphthaIene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (B-28)
A solution of 2,5-dimethyl-benzoic acid (300 mg, 2 mmol) in thionyl chloride (5 mL) was refluxed for 3 h and then concentrated in vacuo. The crude material was used without purification as 2,5-dimethyl-benzoyl chloride. The title compound was made following general procedure in Scheme 3, substituting 4-(4-amino- naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid ethyl ester for 4-amino- naphthalene-l-sulfonic acid (4-methoxy-phenyl)-amide and substituting 2,5- dimethyl-benzoyl chloride for / methoxy-benzoyl chloride. *HNMR (300 MHz, MeOD/CDCl3) δ 8.60 (dd, IH), 8.22 (d, IH), 8.10 (m, IH), 7.98 (m, IH), 7.58 (m, 2H), 7.35 (s, IH), 7.14 (m, 2H), 3.98 (q, 2H), 3.78 (d, 2H), 3.15 (m, IH), 2.68 (m, 2H), 2.42 (s, 3H), 2.32 (s, 3H), 1.55 (m, 2H), 1.20 (m, 2H), 1.12 (t, 3H); LC/MS m/z 510 (M + H)+
Figure imgf000061_0001
N-[4-(4-Methoxy-phenylsulfamoyl)-naphthalen-l-yl]-N-methyl-benzamide (B-
33)
The title compound was made from B-30 following the general procedure in Scheme 3. *H ΝMR (300 MHz, DMSO) δ 8.23 (t, TTT), 8.10 (d, 3H), 7.87 (d, IH), 7.60 (m, 5H), 7.03 (d, TTT), 6.82 (d, TTT), 3.72 (s, 3H), 3.18 (s, 3H); LC/MS m/z 445 (M - H)\
Scheme 4: General procedures for amine deprotections
Figure imgf000061_0002
N-[4-(Piperidin-4-yIsuIfamoyl)-naphthalen-l-yl]-benzamide (12)
4-(4-Benzoylamino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert- butyl ester (11) was prepared following the general procedure in Scheme 2. To a solution of 4-(4-benzoylamino-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester (11) in MeOH was added a solution of 4 Ν HCl in dioxane. The reaction mixture was stirred at 25 °C for 5 h and then concentrated in vacuo. The crude material was purified by reverse phase HPLC to provide the title compound. 1H ΝMR (300 MHz, MeOH) δ 8.75 (d, IH), 8.46 (s, IH), 8.33 (d, IH), 8.21 (d, IH), 8.10 (m, IH), 8.07 (m, IH), 7.83 (d, IH), 7.69 (m, 5H), 3.21 (m, 3H), 2.92 (m, 2H), 1.82 (m, TTT), 1.60 (m, 2H); LC/MS (M + H)+ m/z 410. (±)-(trαws)-4-[4-(2-MethyI-benzoylamino)-naphthalene-l-suIfonylamino]- piperidine-3-carboxylic acid ethyl ester (14)
(±)-(trαrø)-l-Benzyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-3 -carboxylic acid methyl ester 13 was made following general procedure in Scheme 2, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for m-anisidine and 4-(2-methyl-benzoylarnino)-naphthalene-l-sulfonyl chloride for 4-benzoylamino-naphthalene-l-sulfonyl chloride benzylamine. To a solution of l-benzyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-3 -carboxylic acid methyl ester 13 (170 mg, 0.29 mmol) in MeOH was added Pd(OH)2/C 20% wet (80mg). The reaction mixture was stirred at 25 °C under an hydrogen atmosphere overnight. The resultant mixture was filtered and the solvent was concentrated in vacuo to provide the title compound 14. This material was not further purified and used directly in the next reaction.
Scheme 5
Figure imgf000062_0001
N-[4-(Piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-l)
4-(4-Benzoylamino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert- butyl ester (A-38) was prepared following the general procedure in Scheme 2. Deprotection was achieved following the procedure in Scheme 4-1. The reaction mixture was stirred at 25 °C for 5 h and then concentrated in vacuo. The crude material was purified by reverse phase HPLC to provide the title compound. *H ΝMR (300 MHz, MeOH) δ 8.75 (d, IH), 8.46 (s, IH), 8.33 (d, IH), 8.21 (d, IH), 8.10 (m, IH), 8.07 (m, IH), 7.83 (d, IH), 7.69 (m, 5H), 3.21 (m, 3H), 2.92 (m, 2H), 1.82 (m, 2H), 1.60 (m, 2H); LC/MS (M + H)+ m/z 410.
4-(4-Benzoylamino-naphthaIene-l-sulfonylanιino)-piperidine-l-carboxylic acid isopropyl amide (C-2)
To a 25 °C solution of N-[4-(piperidin-4-yl sulfamoyl)-naphthalen-l-yl] -benzamide (C-l) in CH2C12 was added Et3Ν followed by 2-isocyanato-propane. The reaction mixture was stirred at 25° C overnight. Aqueous work-up followed by purification using reverse phase HPLC provided the title compound. 1H NMR (300 MHz, MeOD) δ 8.74 (d, TTT), 8.29 (d, TTT), 8.17 (d, IH), 8.07 (s, IH), 8.05 (s, IH), 7.81 (d, IH), 7.63 (m, 5H), 3.75 (m, 3H), 3.21 (m, IH), 2.68 (t, 2H), 1.51 (m, 2H), 1.26 (m, 2H), 1.05 (d, 6ΪT); LC/MS (M + H)+ m/z 495.
Figure imgf000063_0001
N-{4-[l-(Morpholine-4-carbonyl)-piperidin-4-ylsulfamoyl]-naphthaIen-l-yl}- benzamide (C-4)
The title compound was made following general procedure in Scheme 5, substituting 4-isocyanato-tetrahydro-pyran for 2-isocyanato-propane. H ΝMR (300 MHz, MeOD) δ 8.74 (d, IH), 8.29 (d, IH), 8.17 (d, IH), 8.07 (m, IH), 8.05 (m, IH), 7.81 (d, IH), 7.63 (m, 5H), 3.57 (m, 4H), 3.48 (m, 2H), 3.13 (m, 3H), 2.73 (t, 2H), 2.54 (m, 2H), 1.32 (m, 2H); LC/MS (M + H)+ m/z 523.
Figure imgf000063_0002
N-[4-(l-Cyclopentanecarbonyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-5)
The title compound was prepared following general procedure in Scheme 5, substituting cyclopentanecarbonyl chloride for 2-isocyanato-propane to afford the title compound as a cream colored solid. 1H NMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, IH), 8.19 (d, IH), 8.09 (m, IH), 8.07 (d, IH), 7.82 (d, IH), 7.65 (m, 6H), 4.17 (d, IH), 3.83 (d, IH), 2.97 (m, 2H), 2.65 (m, IH), 1.65 (m, 11H), 1.29 (m, 2H); LC/MS (M + H)+ m/z 506.
Figure imgf000064_0001
4-(4-Benzoylamino-naphthalene-l-sulfonylamino)-piperidine-l-carboxy lie acid ethylamide (C-7)
The title compound was prepared following general procedure in Scheme 5, substituting isocyanato-ethane for 2-isocyanato-propane. !H NMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.30 (d, IH), 8.19 (d, IH 8.08 (d, 2H), 7.82 (d, IH), 7.65 (m, 5H), 3.74 (d, TTT), 3.23 (m, IH), 3.10 (m, TTT), 2.70 (t, 2H), 1.53 (m, 2H), 1.28 (m, TTT), 1.04 (t, 3H); LC/MS (M + H)+ m/z 481.
Figure imgf000064_0002
4-[4-(3-Methyl-benzoyIamino)-naphthaIene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (C-9)
The title compound was made following general procedure in Scheme 5, substituting 4-aminopiperidine-l -carboxylic acid ethyl ester for 4-aminopiperidine-l -carboxylic acid tert-butyl ester and m-tolyl chloride for benzoyl chloride.
Figure imgf000064_0003
c/s-3-[4-(2-Methyl-benzoylamino)-naphthaIene-l-sulfonylamino]-8-aza- bicyclo[3.2.1]octane-8-carboxylic acid ethyl ester (C-10) The title compound was made following general procedure in Scheme 5, substituting cw-3-amino-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid ethyl ester for 4- aminopiperidine-1 -carboxylic acid tert-butyl ester. Η NMR (300 MHz, DMSO) δ 8.75 (d, IH), 8.27 (d, IH), 8.14 (d, IH), 7.75 (d, IH), 7.65 (m, 4H), 7.41 (m, IH), 7.35 (m, 2H), 3.94 (m, 4H), 3.25 (br s, IH); 2.50 (s, 3H), 1.92 (d, 2H), 1.67 (m, 4H), 1.07 (t, 3H); LC/MS m/z 523 (M + H)+.
Figure imgf000065_0001
(±)-iV-[4-(3,3-Dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-ll) The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l-sulfonyl chloride and 4-amino- 3, 3 -dimethyl-piperidine-1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l - carboxylic acid tert-butyl ester. *HNMR (300 MHz, MeOD) δ 8.82 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.93 (d, IH), 7.68 (m, 3H), 7.40 (m, 3H), 3.18 (m, 3H), 3.00 (d, IH), 2.85 (m, 2H); 2.54 (s, 3H), 1.60 (m, 3H), 0.95 (s, 3H), 0.70 (s, 3H); LC/MS m/z 452 (M + H)+.
Figure imgf000065_0002
(±)-cιs-3-Methyl-4-[4-(2-methyI-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid ethylamide (C-12)
The title compounds were made following general procedure in Scheme 5 and deprotection in scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l-sulfonyl chloride, 4-amino- 1- benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl isocyanate for 2-isocyanato-propane. 1H NMR (300 MHz, CDC13) δ 8.71
(d, IH), 8.40 (s, IH), 8.28 (s, 2H), 7.98 (d, IH), 7.68 (m, 3H), 7.41 (m, IH), 7.30 (m, 2H), 5.21(d, IH), 4.36 (m, IH), 3.35 (m, 2H), 3.15 (m, 4H), 2.98 (m, 2H), 2.57 (s, 3H), 1.71 (m, 2H), 1.40 (m, 2H), 1.10 (m, IH), 1.03 (t, 3H) 0.63 (d, 3H); LC/MS m/z 509 (M + TT .
Figure imgf000066_0001
(±)- -3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid isopropyl ester (C-13)
The title compounds were made following the general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid te7*t-butyl ester and isopropyl chloroformate for 2-isocyanato-propane. *H NMR (300 MHz, CDC13) δ 8.72 (d, IH), 8.43 (d, IH), 8.35 (d, IH), 8.12 (d, IH), 7.95 (d, 2H), 7.72 (m, 3H), 7.46 (m, IH), 7.35(d, 2H), 4.85 (m, IH), 4.66 (d, IH), 3.55 (m, IH), 3.37 (m, IH), 3.17 (m, 2H), 2.59 (s, 3H), 1.74 (m, IH), 1.58 (m, IH), 1.40 (m, 2H) 1.18 (dd, 6H), 0.67 (m, 3H); LC/MS m/z 524 (M + H)+.
Figure imgf000066_0002
(±)-trαn-.-2-Methyl-N-[4-(3-methyl-piperidin-4-ylsulfamoyI)-naphthalen-l-yl]- benzamide (C-14)
The title compound was made following general procedure in Scheme 5 and flash column chromatography (Hexane/EtOAc, gradient) followed by deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride and (±)-4-amino-l- benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 'H ΝMR (300 MHz, MeOD) δ 8.77 (d, IH), 8.48 (s, IH), 8.32 (d, IH), 8.24 (d, IH), 7.94 (d, IH), 7.75 (m, 3H), 7.40 (m, 3H), 3.25 (m, IH), 2.90 (m, 2H), 2.55 (s, 3H), 1.60 (m, 3H), 0.65 (d, 3H); LC/MS m/z 438 (M + H)+.
Figure imgf000067_0001
2-Methyl-N-[4-(4-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-15)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride and 4-amino- 4-methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine- 1 - carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, DMSO) δ 8.73 (d, IH), 8.68 (br s, IH), 8.28 (d, IH), 8.23 (d, IH), 7.95 (d, IH), 7.70 (m, 3H), 7.40 (m, 3H), 2.90 (m, 4H), 2.48 (s, 3H), 2.00 (m, 2H), 1.58 (m, 2H), 0.95 (s, 3H); LC/MS m/z 438 (M + H)+.
Figure imgf000067_0002
(±)-trα«s-3-Methyl-4-[4-(2-methyl-benzoyIamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethylamide (C-16)
The title compounds were made following general procedure in Scheme 5 and deprotection in scheme 4- 1 , substituting 4-(2-methyl-benzoylamino)-naphthalene- 1 - sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino-l- benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl isocyanate for 2-isocyanato-propane. 1H NMR (300 MHz, DMSO) δ 8.77 (d, TTT), 8.29 (d, IH), 8.23 (d, IH), 7.91 (d, IH), 7.70 (m, 3H), 7.36 (m, 3H), 3.82 (m, TTT), 3.12 (q, TTT), 2.82 (m, IH), 2.58 (m, IH), 2.55 (s, 3H), 2.31 (t, IH), 1.40 (m, 2H), 1.20 (m, IH), 1.03 (t, 3H), 0.59 (d, 3H); LC/MS m/z 509 (M + H)+.
Figure imgf000068_0001
(±)-trαns-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-17)
The title compound was made following general procedure in scheme 5 and deprotection in scheme 4, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl chloroformate for 2-isocyanato-propane. Flash column chromatography (Hexane/EtOAc, gradient) of the mixture gave C-17. *H NMR (300 MHz, CDC13) δ 8.77 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.92 (d, IH), 7.73 (m, 3H), 7.35 (m, 3H), 4.03 (q, 2H), 3.94 (t, 2H), 2.85 (dt, IH), 2.64 (m, IH), 2.55 (s, 3H), 2.40 (m, IH), 1.48 (m, IH), 1.38 (m, IH), 1.20 (t, 3H), 0.59 (d, 3H); LC/MS m/z 510 (M + H)+.
Figure imgf000068_0002
(±)-tr «s-3-methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyIamino]-piperidine-l-carboxylic acid isopropyl ester (C-18)
The title compounds were made following the general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and isopropyl chloroformate for 2-isocyanato-propane. C-18: *H NMR (300 MHz, CDC13) δ 8.70 (d, IH), 8.40 (m, 2H), 8.17 (s, IH), 7.95 (d, IH), 7.70 (m, 3H), 7.44 (m, IH), 7.34 (m, 2H), 4.80 (m, IH), 4.58 (d, IH), 3.90 (d, 2H), 2.87 (m, IH), 2.60 (m, IH), 2.59 (s, 3H), 2.33 (m, IH), 1.65 (m, IH), 1.32 (m, IH), 1.18(d, 6H), 0.60 (br s, 3H); LC/MS m/z 524 (M + H)+.
Figure imgf000069_0001
(±)-tr «5-N-[4-(l-Butyryl-3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- 2-methyl-benzamide (C-19)' The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3-methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and butyryl chloride for 2-isocyanato-propane. Flash column chromatography (Hexane/EtOAc, gradient) of the mixture gave C-19. 1H ΝMR (300 MHz, CDC13) δ 8.70 (t, IH), 8.33 (m, 3H), 7.95 (d, IH), 7.62 (m, 3H), 7.40 (m, IH), 7.34 (m, TTT), 5.00 (d, IH), 4.30 (dd, IH), 3.63 (m, TTT), 2.85 (m, 1.5H), 2.57 (s, 3H), 2.40 (t, 0.5H), 2.15 (m, 1.5H), 2.09 (m, 0.5H), 1.83 (m, 0.5H), 1.50 (m, 1.5H); LC/MS m/z 508 (M + H)+.
Figure imgf000069_0002
piperidine-l-carboxylic acid ethyl ester (C-20)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4- 1 , substituting 4-(2-methyl-benzoylamino)-naphthalene- 1 - sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3,3-dimethyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl chloroformate for 2-isocyanato-propane. !H ΝMR (300 MHz, DMSO) δ 8.75 (d, IH), 8.24 (m, 2H), 7.93 (d, IH), 7.77 (d, IH), 7.66 (m, 3H), 7.40 (m, 3H), 3.98 (q, 2H), 3.69 (m, IH), 3.43 (d, IH), 2.96 (m, IH), 2.60 (m, IH), 2.48 (s, 3H), 1.33 (m, IH), 1.15 (m, IH), 1.10 (t, 3H), 0.68 (s, 3H), 0.50 (s, 3H); LC/MS
Figure imgf000070_0001
(±)-3,3-Dimethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid ethylamide (C-21)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-ammo- l-benzyl-3,3-dimethyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl isocyanate for 2-isocyanato-propane. *H NMR (300 MHz, DMSO) δ 8.76 (d, IH), 8.26 (m, 2H), 7.92 (d, IH), 7.65 (m, 4H), 7.38 (m, 3H), 6.24 (m, IH), 3.65 (d, IH), 3.48 (d, IH), 3.48 (d, IH), 2.90 (m, 3H), 2.47 (s, 3H), 2.42 (m, 3H), 1.25 (m, IH), 1.00 (m, IH), 0.91 (t, 3H), 0.68 (s, 3H), 0.53 (s, 3H); LC/MS m/z 523 (M + H)+.
Figure imgf000070_0002
(±)-3,3-Dimethyl-4-[4-(2-methyl-benzoyIamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid isopropyl ester (C-22) The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl~benzoylammo)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3,3-dimethyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert- butyl ester and isopropyl chloroformate for 2-isocyanato-propane. "H NMR (300 MHz, DMSO) δ 8.75 (d, IH), 8.25 (m, 2H), 7.93 (d, IH), 7.70 (m, 3H), 7.38 (m, 3H), 4.66 (m, IH), 3.68 (m, IH), 3.43 (d, IH), 2.94 (m, IH), 2.55 (m, 2H), 2.47 (s, 3H), 1.30 (m, IH), 1.10 (d, 6H), 0.67 (s, 3H), 0.50 (s, 3H); LC/MS m/z 538 (M + H)+.
Figure imgf000071_0001
(±)-iV-[4-(l-Butyryl-3,3-dimethyI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-23)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, (±)-4-amino- l-benzyl-3,3-dimethyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert- butyl ester and butyryl chloride for 2-isocyanato-propane. *H NMR (300 MHz, DMSO) δ 8.77 (dd, IH), 8.25 (m, 2H), 7.93 (d, IH), 7.70 (m, 4H), 7.38 (m, 3H), 4.06 (d, 0.5H), 3.85 (d, 0.5H), 3.60 (d, 0.5H), 3.37 (d, 0.5H), 2.98 (m, IH), 2.77 (m, IH), 2.47 (s, 3H), 2.35 (d, 0.5H), 2.16 (m, 2H), 1.40 (m, 2H), 1.24 (m, 0.5H), 1.11 (m, 0.5H), 0.80 (t, 3H), 0.70 (s, 1.5H), 0.64 (s, 1.5H), 0.55 (s, 3H); LC/MS m/z 522 (M + H)+.
Figure imgf000071_0002
4-Methyl-4-[4-(2-methyl-benzoyIamino)-naphthaIene-l-sulfonyIamino]- piperidine-1-carboxylic acid ethylamide (C-24)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene- 1- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, and 4-amino- 4-methyl-piperidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l - carboxylic acid tert-butyl ester and ethyl isocyanate for 2-isocyanato-propane. !H NMR (300 MHz, DMSO) δ 8.76 (d, IH), 8.24 (m, 2H), 7.93 (d, IH), 7.38 (m, 3H), 7.70 (m, 4H), 6.26 (t, IH), 3.18 (m, TTT), 2.93 (m, 2H), 2.78 (m, 2H), 2.47 (s, 3H), 1.69 (m, 2H), 1.24 (m, TTT), 1.09 (s, 3H), 0.90 (t, 3H); LC/MS m/z 509 (M + H)+.
Figure imgf000072_0001
4-Methyl-4- [4-(2-methyl-benzoylamino)-naphthalene-l-sulf onylamino] - piperidine-1-carboxylic acid ethyl ester (C-25)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino-4- methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine- 1 - carboxylic acid tert-butyl ester and ethyl chloroformate for 2-isocyanato-propane. 1H NMR (300 MHz, MeOD) δ 8.80 (d, IH), 8.29 (m, IH), 8.23 (d, IH), 7.93 (d, IH), 7.65 (m, 3H), 7.38 (m, 3H), 4.02 (q, 2H), 3.43 (m, 2H), 2.90 (m, 2H), 2.54 (s, 3H), 1.87 (m, 2H), 1.15 (m, 6H); LC/MS m/z 510 (M + H)+.
Figure imgf000072_0002
4-MethyI-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid isopropyl ester (C-26)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4- 1 , substituting 4-(2-methyl-benzoylamino)-naphthalene- 1 - sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino-4- methyl-piperidine-1 -carboxylic acid tert-butyl ester for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester. 'HNMR (300 MHz, MeOD) δ 8.80 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.93 (d, IH), 7.75 (m, 3H), 7.35 (m, 3H), 4.79 (q, 2H), 3.40 (m, 2H), 2.88 (t, 2H), 1.86 (m, 2H), 1.37 (m, 6H), 1.10 (m, 9H); LC/MS m/z 524 (M + H)+.
Figure imgf000073_0001
N-[4-(l-Butyryl-4-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-27)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino-4- methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine- 1 - carboxylic acid tert-butyl ester and butyryl chloride for 2-isocyanato-propane. *H ΝMR (300 MHz, DMSO) δ 8.76 (d, IH), 8.26 (m, 2H), 7.95 (d, IH), 7.70 (m, 3H), 7.34 (m, 3H), 3.54 (m, IH), 3.31 (m, TTT), 3.04 (m, IH), 2.76 (m, IH), 2.47 (s, 3H), 2.09 (t, 3H), 1.82 (m, 2H), 1.30 (m, 6H), 1.07 (s, 3H), 0.77 (t, 3H); LC/MS m/z 508 (M + H)+.
Figure imgf000073_0002
(±)-c/5-2-Methyl-N-[4-(3-methyl-piperidin-4-ylsuIfamoyl)-naphthaIen-l-yI]- benzamide (C-28) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride and (±)-4-amino-l-benzyl-3 -methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. Purification of the benzyl- protected intermediate by Flash column chromatography (Hexane/EtOAc, gradient) followed by deprotection according to Scheme 4-2 gave C-28. *H ΝMR (300 MHz, MeOD) δ 8.82 (d, TTT), 8.52 (s, IH), 8.32 (d, IH), 8.24 (d, 2H), 7.94 (d, 2H), 7.70 (m, 3H), 7.4 (m, 3H), 3.46 (m, IH), 3.00 (m, 2H), 2.97 (m, IH), 2.55 (s, 3H), 1.93 (m, IH), 1.64 (m, 2H), 0.63 (d, 3H); LC/MS m/z 438 (M + H)+.
Figure imgf000074_0001
(±)-c s-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonyIamino]- piperidine-1-carboxylic acid dimethylamide (C-29)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-2, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino- 1- benzyl-3 -methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and dimethylcarbamyl chloride for 2-isocyanato-propane. !H NMR (300 MHz, CDC13) δ 8.71 (d, IH), 8.41 (s, IH), 8.28 (s, IH), 7.97 (d, IH), 7.62 (m, 3H), 7.41 (m, IH), 7.28 (m, 2H), 5.27 (d, IH), 3.38 (m, IH), 3.11 (m, IH), 2.99 (dd, IH), 2.88 (m, 2H), 2.70 (s, 6TT), 2.56 (s, 3H), 1.46 (m, IH), 1.42 (m, 2H), 0.63 (d, 3H); LC/MS m/z 509 (M + H)+.
Figure imgf000074_0002
(±)-c -.-N-[4-(l-AcetyI-3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-30) The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-2, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino- 1- benzyl-3 -methyl-piperidine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and acetyl chloride for 2-isocyanato-propane. 1H ΝMR (300 MHz, CDC13) δ 8.74 (m, IH), 8.33 (br s, 3H), 7.98 (d, IH), 7.63 (m, 3H), 7.42 (m, IH), 7.26 (m, 2H), 5.29 (d, IH), 3.78 (m, 0.5H), 3.38 (m, 1.5H), 3.20 (m, 1.5H), 2.97 (m, 0.5H), 2.57 (s, 3H), 2.08 (m, 1.5H), 1.96 (d, 3H), 1.83 (m, 0.5H), 1.45 (m, 2H), 0.72 (d, 1.5H), 0.56 (d, 1.5H); LC/MS m/z 480 (M + H)+.
Figure imgf000075_0001
2-methyl-benzamide (C-31)
The title compound was made following general procedure in Scheme 5 and deprotection in Scheme 4-1, substituting 4-(2-methyl-benzoylamino)-naphthalene-l- 0 sulfonyl chloride for 4-benzoylamino-naphthalene-l -sulfonyl chloride, 4-amino-4- methyl-piperidine-1 -carboxylic acid tert-butyl ester for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester and acetyl chloride for 2-isocyanato-propane. !H ΝMR (300 MHz, CDC13) δ 8.70 (m, IH), 8.35 (m, 3H), 7.95 (d, IH), 7.65 (m, 3H), 7.40 (m, IH), 7.26 (m, TTT), 5.02 (d, IH), 4.30 (m, IH), 3.58 (m, IH), 2.95 (m, TTT), 5 2.62 (m, 0.5H), 2.58 (s, 3H), 2.45 (m, 0.5H), 1.98 (s, 3H), 1.75 (m, IH), 1.25 (m, 2H), 0.70 (d, 1.5H), 0.51 (d, 1.5H); LC/MS m/z 480 (M + H)+.
Figure imgf000075_0002
(±)-Λ'-[4-(l-5ec-Butyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyI- 0 benzamide (C-32)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and butan-2-one/sodium triacetoxyborohydride for 2-isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 5 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.39 (m, IH), 3.15 (m, 3H), 2.98 (m, 2H), 2.55 (s, 3H), 1.88 (m, 2H), 1.72 (m, 3H), 1.43 (m, IH), 1.19 (d, 3H), 0.95 (t, 3H); LC/MS (M + H)+ m/z 480.
Figure imgf000076_0001
2-Methyl-N-{4-[l-(morphoIine-4-carbonyl)-piperidin-4-ylsulfamoyl]- naphthalen-l-yl}-benzamide (C-33) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and morpholine-4-carbonyl chloride for 2- isocyanato-propane. 'H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.59 (t, 4H), 3.50 (m, 2H), 3.27 (m, IH), 3.19 (t, 4H), 2.76 (m, 2H), 2.54 (s, 3H), 1.59 (m, TT ), 1.27 (m, 2H); LC/MS (M + H)+ m/z 537.
Figure imgf000076_0002
4-[4-(2-Methyl-benzoyIamino)-naphthalene-l-suIfonyIamino]-piperidine-l- carboxylic acid ethylamide (C-34)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, and isocyanato-ethane for 2-isocyanato-propane. *H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.73 (m, 2H), 3.23 (m, IH), 3.11 (q, 2H), 2.69 (m, 2H), 2.54 (s, 3H), 1.53 (m, TTT), 1.29 (m, 2H), 1.04 (t, 3H); LC/MS (M + H)+ m/z 495.
Figure imgf000076_0003
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl-benzamide
(C-35)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and butyryl chloride for 2-isocyanato-propane. *H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 4.19 (m, IH), 3.74 (m, IH), 3.33 (m, IH), 3.01 (m, IH), 2.64 (m, IH), 2.54 (s, 3H), 2.74 (t, 2H), 1.62 (m, 2H), 1.55 (m, 2H), 1.29 (m, 2H), 0.89 (t, 3H); LC/MS (M + H)+ m/z 496.
Figure imgf000077_0001
2-Methyl-N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-36)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-1-sulfonyl chloride. 1H ΝMR (300 MHz, MeOD) δ 8.75 (d, TTT), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.49 (m, IH), 3.15 (m, 2H), 2.90 (m, 2H), 2.50 (s, 3H), 2.21 (m, IH), 1.82 (m, 2H), 1.59 (m, IH) ); LC/MS (M + H)+ m/z 424.
Figure imgf000077_0002
4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonyIamino]-piperidine-l- carboxylic acid isopropyl ester (C-37)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, and isopropyl chloroformate for 2-isocyanato- propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 4.80 (m, IH), 3.83 (m, TTT), 3.25 (m, IH), 2.79 (m, 2H), 2.54 (s, 3H), 1.58 (m, 2H), 1.29 (m, 2H), 1.20 (t, 3H); LC/MS (M + H)+ m/z 510.
Figure imgf000078_0001
N-[4-(l-CyclopentanecarbonyI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- ethyl-benzamide (C-38) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and cyclopentanecarbonyl chloride for 2- isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.41 (m, 3H), 4.19 (m, IH), 3.88 (m, IH), 3.00 (m, 2H), 2.68 (m, TTT), 2.54 (s, 3H), 1.65 (m, 11H), 1.29 (m, 3H); LC/MS (M + H)+ m/z 520.
Figure imgf000078_0002
N-[4-(l-Cyclopropanecarbonyl-piperidin-4-ylsulfamoyl)-naphthaIen-l-yl]-2- methyl-benzamide (C-39)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and cyclopropanecarbonyl chloride for 2- isocyanato-propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.41 (m, 3H), 4.17 (m,*2H), 3.13 (m, IH), 2.71 (m, 2H), 2.54 (s, 3H), 1.84 (m, IH), 1.71 (m, IH), 1.59 (m, IH), 1.29 (m, 2H), 0.79 (m, 4H); LC/MS (M + H)+ m/z 492.
Figure imgf000078_0003
-V-{4-[l-(Imino-pyrrolidin-l-yl-methyl)-piperidin-4-ylsulfamoyl]-naphthalen-l- yI}-2-methyl-benzamide (C-40) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and pyrrolidine-1-carbonitrile for 2-isocyanato- propane. Η NMR (300 MHz, DMSO) δ 8.70 (d, IH), 8.49 (s, IH), 8.28 (d, IH), 8.21 (d, IH), 7.93 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.40 (m, 9H), 2.98 (m, 2H), 2.54 (s, 3H), 1.82 (m, 4H), 1.60 (m, IH), 1.39 (m, IH); LC/MS (M + H)+ m/z 520.
Figure imgf000079_0001
4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid methylamide (C-41)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and isocyanatomethane for 2-isocyanato-propane. H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.73 (m, 2H), 3.25 (m, IH), 2.72 (m, 2H), 2.65 (s, 3H), 2.56 (s, 3H), 1.53 (m, TTT), 1.28 (m, TTT); LC/MS (M + H)+ m/z 481.
Figure imgf000079_0002
4-[4-(2-MethyI-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid diethylamide (C-42)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and diethylcarbamyl chloride for 2-isocyanato- propane. 1H NMR (300 MHz, MeOD) δ 8.78 (d, TTT), 8.33 (d, TTT), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.41 (m, 2H), 3.23 (m, IH), 3.15 (q, 4H), 2.72 (m, 2H), 2.56 (s, 3H), 1.53 (m, TTT), 1.40 (m, 2H), 1.07 (t, 6H); LC/MS (M + H)+ m/z 523.
Figure imgf000080_0001
2-Methyl-N-{4-[l-(pyrrolidine-l-carbonyl)-piperidin-4-ylsulfamoyl]- naphthalen-l-yl}-benzamide (C-43)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and pyrrolidine-1 -carbonyl chloride for 2- isocyanato-propane. *H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.55 (m, 2H), 3.25 (m, 5H), 2.72 (m, 2H), 2.56 (s, 3H), 1.72 (m, 4H ), 1.59 (m, 2H), 1.38 (m, 2H); LC/MS (M + H)+ m/z 521.
Figure imgf000080_0002
2-Methyl-N-{4-[l-(piperidine-l-carbonyl)-piperidin-4-ylsulfamoyl]-naphthalen- l-yl}-benzamide (C-44) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and piperidine-1 -carbonyl chloride for 2- isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.39 (m, 3H), 3.41 (m, 4H), 3.15 (m, 5H), 2.72 (m, 2H), 2.56 (s, 3H), 1.58 (m, 8H); LC/MS (M + H)+ m/z 535.
Figure imgf000080_0003
4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonyIamino]-piperidine-l- carboxylic acid propylamide (C-45) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and 1-isocyanato-propane for 2-isocyanato- propane. 1H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.75 (m, 2H), 3.25 (m, IH), 3.06 (t, 2H), 2.74 (m, 2H), 2.59 (s, 3H), 1.59 (m, 2H), 1.49 (m, 2H), 1.30 (m, 2H), 0.89 (t, 3H); LC/MS (M + H)+ m/z 509.
Figure imgf000081_0001
4-[4-(2-MethyI-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid isopropylamide (C-46)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride. 'H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, TTT), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H),7.43 (m, IH ), 7.38 (m, TTT), 3.76 (m, 2H), 3.25 (m, 2H), 2.71 (m, 2H), 2.57 (s, 3H), 1.59 (m, 2H), 1.30 (m, TTT), 1.05 (d, 6H); LC/MS (M + H)+ m/z 509.
Figure imgf000081_0002
4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid dimethylamide (C-47)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, and dimethylcarbamyl chloride for 2-isocyanato- propane. 1H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, TTT), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.54 (m, 2H), 3.25 (m, IH), 2.75 (s, 6TT), 2.71 (m, 2H), 2.55 (s, 3H), 1.59 (m, TTT), 1.35 (m, TTT); LC/MS (M + H)+ m/z 495.
Figure imgf000082_0001
(±)-2-Methyl-N-[4-(pyrrolidin-3-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-
48)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 3 -amino-pyrrolidine-1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. *H ΝMR (300 MHz, DMSO) δ 8.78 (d, IH), 8.33 (m, 2H), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, TTT), 3.69 (m, IH), 3.88 (m, 3H), 2.61 (m, IH ), 2.48 (s, 3H), 1.74 (m, IH), 1.49 (m, IH); LC/MS (M + H)+ m/z 410.
Figure imgf000082_0002
N-[4-(l-Acetyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl-benzamide (C-49)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, and acetyl chloride for 2-isocyanato-propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.15 (m, IH), 3.69 (m, IH), 3.25 (m, IH), 3.03 (m, IH ), 2.69 (m, IH), 2.55 (s, 3H), 1.98 (s, 3H), 1.59 (m, TTT), 1.31 (m, 2H); LC/MS (M + H)+ m/z 466.
Figure imgf000082_0003
2-Methyl-N-[4-(l-propionyI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-50)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and propionyl chloride for 2-isocyanato-propane. lR ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.19 (m, IH), 3.72 (m, IH), 3.25 (m, IH), 3.01 (m, IH ), 2.69 (m, IH), 2.55 (s, 3H), 2.41 (q, 2H), 1.61 (m, 2H), 1.31 (m, 2H), 1.02 (t, 3H); LC/MS (M + H)+ m/z 480.
Figure imgf000083_0001
N-[4-(l-Isobutyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-51)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene- 1 -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and isobutyryl chloride for 2-isocyanato-propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.20 (m, IH), 3.72.
Figure imgf000083_0002
(±)-3-[4-(2-Methyl-benzoyIamino)-naphthaIene-l-sulfonyIamino]-pyrrolidine-l- carboxylic acid ethylamide (C-52)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, 3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and isocyanato-ethane for 2-isocyanato-propane. 'HΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (m, 2H), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.80 (m, IH), 3.19 (m, IH), 3.11 (q, 2H), 3.09 (m, 3H ), 2.55 (s, 3H), 1.89 (m, IH), 1.73 (m, IH), 1.03 (t, 3H); LC/MS (M + H)+ m/z 481.
Figure imgf000084_0001
(±)-3-[4-(2-MethyI-benzoylamino)-naphthalene-l-sulfonylamino]-pyrrolidine-l- carboxylic acid ethylamide (C-53)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and butyryl chloride for 2-isocyanato-propane. 'HNMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (m, 2H), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.85 (m, IH), 3.40 (m, 3H), 3.15 (m, IH), 2.53 (s, 3H), 2.19 (t, IH), 1.95 (t, IH), 1.85 (m, 2H), 1.50 (m, 2H), 0.88 (m, 3H); LC/MS (M + H)+ m/z 480.
Figure imgf000084_0002
(±)-3-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-pyrrolidine-l- carboxylic acid ethyl ester (C-54)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl chlorofomate for 2-isocyanato-propane. *H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (m, 2H), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.06 (m, 2H), 3.80 (m, IH), 3.38 (m, IH), 3.25 (m, IH ), 3.09 (m, 2H), 2.55 (s, 3H), 1.89 (m, IH), 1.73 (m, IH), 1.20 (m, 3H); LC/MS (M + H)+ m/z 483.
Figure imgf000085_0001
N-{4-[l-(2-Dimethylamino-acetyI)-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}-2- methyl-benzamide (C-55)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and dimethylamino-acetyl chloride for 2- isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, TTT), 4.18 (m, IH), 3.94 (d, TTT), 3.54 (m, IH), 3.34 (m, IH), 3.03 (m, IH ), 2.80 (m, IH), 2.77 (s, 6H), 2.55 (s, 3H), 1.68 (m, 2H), 1.39 (m, TTT); LC/MS (M + H)+ m/z 509.
Figure imgf000085_0002
N-{4-[l-(2-Methoxy-acetyl)-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}-2- methyl-benzamide (C-56) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and methoxy-acetyl chloride for 2-isocyanato- propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.15 (m, IH), 4.04 (d, 2H), 3.94 (d, 2H), 3.63 (m, IH), 3.34 (s, 3H), 3.32 (m, IH ), 3.01 (m, IH ), 2.71 (m, IH), 2.55 (s, 3H), 1.63 (m, TTT), 1.41 (m, 2H); LC/MS (M + H)+ m/z 496.
Figure imgf000085_0003
2-MethyI-N-[4-(l-pyrimidin-2-yl-piperidin-4-yIsuIfamoyl)-naphthalen-l-yI]- benzamide (C-57) The title compound was made following general procedure in Scheme 5, substituting 4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting 2-bromo-pyrimidine for 2-isocyanato-propane. *H NMR (300 MHz, CDCl3/MeOD) δ 8.57 (d, IH), 8.19 (d, 2H), 8.08 (d, 2H), 7.97 (d, 2H), 7.52 (m, 3H), 7.27 (t, IH), 7.18 (d, 2H), 6.32 (t, IH), 4.30 (d, 2H), 3.93 (s, 3H), 3.21 (m, IH), 2.79 (dt, TTT), 2.43 (s, 3H), 1.58 (m, TTT), 1.20 (m, 3H); LC/MS m/z 500 (M - H)'
Figure imgf000086_0001
N-[4-(l-Benzenesulfonyl-piperidin-4-yIsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-58)
The title compound was made following general procedure in Scheme 5, substituting 4- [4-(2-methyl-benzoylamino)-naphthalene- 1 -sulfonylamino] -piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene- 1 - sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting benzenesulfonyl chloride for 2-isocyanato-propane. 1H ΝMR (300 MHz, CDC13) δ 8.60 (d, IH), 8.22 (m, 3H), 7.94 (d, IH), 7.48 (m, 11H), 4.57 (d, IH), 3.49 (m, 2H), 3.02 (s, br, IH), 2.55 (s, 3H), 2.28 (t, TTT), 1.60 (m, 2H), 1.40 (m, 2H); LC/MS m/z 564 (M + H)+
Figure imgf000086_0002
2-Methyl-N-{4-[l-(propane-l-sulfonyl)-piperidin-4-ylsulfamoyl]-naphthalen-l- yl}-benzamide (C-59) The title compound was made following general procedure in Scheme 5, substituting 4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting propane- 1 -sulfonyl chloride for 2-isocyanato-propane. *H NMR (300 MHz, MeOD/CDCl3) δ 8.69 (d, IH), 8.27 (d, IH), 8.17 (d, IH), 7.97 (m, IH), 7.62 (m, 4H), 7.34 (m, 2H), 3.50 (d, 2H), 3.15 (m, IH), 2.75 (m, 4H), 2.54 (s, 3H), 1.68 (m, 4H), 1.45 (m, 2H), 1.00 (s, 3H); LC/MS m/z 528 (M - H)"
Figure imgf000087_0001
N- [4-(l -Benzooxazol-2-yl-piperidin-4-yIsuIfamoyl)-naphthaIen- l-yl] -2-methyl- benzamide (C-60)
The title compound was made following general procedure in Scheme 5, substituting 4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene- 1 - sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting 2-chloro-benzooxazole for 2-isocyanato-propane. !H NMR (300 MHz, MeOD/CDCl3) δ 8.47 (dd, IH), 8.08 (d, TTT), 8.94 (m, IH), 7.80 (m, IH), 7.44 (m, 3H), 7.12 (m, 3H), 6.98 (t, TTT), 6.89 (td, IH), 6.76 (td, IH), 3.75 (d, 2H), 3.10 (m, IH), 2.75 (td, 2H), 2.30 (s, 3H), 1.50 (m, TTT), 1.25 (m, TTT); LC/MS m/z 528 (M + H)+
Figure imgf000087_0002
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2,3-dimethyl- benza ide (C-61)
The title compound was made following general procedure in Scheme 5, substituting 4-[4-(2,3 -dimethyl-benzoylamino)-naphthalene- 1 -sulfonylamino]-piperidine- 1 - carboxylic acid te7-t-butyl ester for 4-(4-benzoylamino-naphthalene- 1 - sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting butyl chloride for 2-isocyanato-propane. ^ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.32 (d, IH), 8.22 (d, IH), 7.96 (m, IH), 7.71 (m, 2H), 7.46 (m, IH), 7.29 (m, 2H), 4.35 (d, IH), 3.75 (d, IH), 3.02 (t, IH), 2.65 (m, IH), 2.45 (s, 3H), 2.35 (s, 3H), 2.25 (m, IH), 1.60 (m, 4H), 1.28 (m, 2H), 2.75 (m, 2H), 0.90 (m, 5H); LC MS m/z 508 (M + H)+
Figure imgf000088_0001
4-[4-(2,3-Dimethyl-benzoylamino)-naphthaIene-l-sulfonyIamino]-piperidine-l- carboxylic acid isopropyl ester (C-62)
The title compound was made following general procedure in Scheme 5, substituting 4- [4-(2,3 -dimethyl-benzoylamino)-naphthalene- 1 -sulfonylamino] -piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting isopropyl chloroformate for 2-isocyanato-propane. *H ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, IH), 8.22 (d, IH), 7.96 (m, IH), 7.71 (m, 2H), 7.46 (m, IH), 7.29 (m, 2H), 4.78 (m, IH), 3.82 (d, 2H), 3.25 (m, IH), 2.75 (m, 2H), 2.45 (s, 3H), 2.35 (s, 3H), 1.50 (m, 2H), 1.25 (m, TTT), 1.15 (d, 6H); LC/MS m/z 524 (M + H)+
Figure imgf000088_0002
4-[4-(2,3-Dimethyl-benzoylamino)-naphthalene-l-sulfonyIamino]-piperidine-l- carboxylic acid ethylamide (C-63)
The title compound was made following general procedure in Scheme 5, substituting 4-[4-(2,3 -dimethyl-benzoylamino)-naphthalene- 1 -sulfonylamino]-piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-benzoylamino-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (A-28), and substituting isocyanato-ethane for 2-isocyanato-propane. 1H NMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.31 (d, IH), 8.22 (d, IH), 7.96 (m, IH), 7.71 (m, 2H), 7.46 (m, IH), 7.29 (m, 2H), 3.75 (d, 2H), 3.82 (d, TTT), 3.25 (m, IH), 3.10 (q, 2H), 2.72 (t, 2H), 2.45 (s, 3H), 2.35 (s, 3H), 1.55 (m, 2H), 1.25 (m, 2H), 1.05 (t, 3H); LC/MS m/z 509 (M + H)+
Figure imgf000089_0001
(±)-(c s,trα«5')-N-[4-(3,5-Dimethyl-piperidin-4-ylsuIfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-64)
The title compound was made following general procedure in scheme 4-2, substituting (±)-l-benzyl-3,5-dimethyl-piperidin-4-ylamine (5) for (±)-4-amino-l- benzyl-piperidine-3 -carboxylic acid ethyl ester (6). H ΝMR (300 MHz, CDC13) δ 8.65 (d, IH), 8.35 (s, IH), 8.18 (d, TTT), 8.05 (m, 2H), 7.55 (m, 3H), 7.30 (m, IH), 7.20 (m, 2H), 3.85 (s, br, TTT), 3.05 (m, 2H), 2.80 (m, 2H), 2.50 (s, 3H), 2.40 (m, IH), 1.85 (m, 2H), 0.63 (dd, 6H); LC/MS m/z 453 (M + H)+
Figure imgf000089_0002
(±)-(cw,trflns)-3,5-Dimethyl-4-[4-(2-methyI-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid dimethylamide (C-65) The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, trαrø)-N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-64) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting dimethylcarbamyl chloride for 2-isocyanato- propane. !H ΝMR (300 MHz, CDC13) δ 8.75 (d, IH), 8.34 (m, 2H), 8.21 (s, IH), 7.95 (d, IH), 7.65 (m, 3H), 7.43 (m, IH), 7.34 (m, 2H), 4.85 (m, IH), 3.44 (d, IH), 3.18 (d, IH), 2.90 (m, 2H), 2.73 (s, 6H), 2.56 (s, 3H), 2.37 (dd, IH), 1.74 (m, 2H), 0.71 (d, 3H), 0.59 (d, 3H); LC/MS m/z 524 (M + H)+
Figure imgf000090_0001
(±)-(c/5,tra«5,)-N-[4-(l-Butyryl-3,5-dimethyl-piperidin-4-ylsulfamoyI)- naphthalen-l-yl]-2-methyl-benzamide (C-66)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, trarø)-N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzarnide (C-64) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l -yl]- benzamide (C-l) and substituting butyl chloride for 2-isocyanato-propane. *H ΝMR (300 MHz, CDC13) δ 8.74(d, IH), 8.33 (m, 3H), 7.96 (m, IH), 7.64 (m, 3H), 7.42 (m, IH), 7.31 (m, 2H), 5.12 (m, IH), 3.60 (m, 2H), 3.18 (d, IH), 3.00 (m, 2H), 2.56 (s, 3H), 2.15 (m, 2H), 1.80 (m, 2H), 1.55 (m, 3H), 0.86 (m, 3H), 0.68 (m, 3H), 0.49 (m, 3H); LC/MS m/z 523 (M + H)+
Figure imgf000090_0002
(±)-(cis,tr /w)-3,5-Dimethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-67) The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, tra«^-N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-64) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting ethyl chlorofonnate for 2-isocyanato-propane. *H ΝMR (300 MHz, CDC13) δ 8.75 (d, IH), 8.35 (m, 2H), 8.19 (s, IH), 7.95 (d, IH), 7.66 (m, 3H), 7.38 (m, 3H), 4.79 (d, IH), 4.05 (m, 2H), 3.74 (m, 2H), 2.95 (m, 2H), 2.59 (s, 3H), 2.40 (m, 1H),1.80 (s, br, TTT), 1.18 (t, 3H), 0.62 (m, 6H); LC/MS m/z 525 (M + H)+
Figure imgf000091_0001
(±)-(c/s,c 5)--V-[4-(3,5-DimethyI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-68)
The title compound was made following general procedure in Scheme 4-2, substituting (±)-l-benzyl-3,5-dimethyl-piperidin-4-ylamine (5) for (±)-4-amino-l- benzyl-piperidine-3-carboxylic acid ethyl ester (6). *H ΝMR (300 MHz, CDC13) δ 8.75 (d, IH), 8.39 (s, IH), 8.16 (d, IH), 8.05 (m, TTT), 7.58 (m, 3H), 7.32 (m, IH), 7.20 (m, 2H), 3.75 (s, br, IH), 3.45 (s, IH), 2.75 (m, 2H), 2.56 (m, 2H), 2.45 (s, 3H), 1.82 (m, 2H), 0.40 (d, 6H); LC/MS m/z 453 (M + H)+
Figure imgf000091_0002
(±)-(c s,cw)-N-[4-(l-Butyryl-3,5-dimethyl-piperidin-4-yIsulfamoyl)-naphthalen- l-yl]-2-methyl-benzamide (C-69)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cw, cw)- N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-68) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting butyl chloride for 2-isocyanato-propane. 'H ΝMR (300 MHz, CDC13) δ 8.80 (d, IH), 8.28 (m, 3H), 7.96 (d, IH), 7.64 (m, 3H), 7.42 (m, IH), 7.32 (m, 2H), 5.16 (d, IH), 4.18 (dd, IH), 3.51 (d, IH), 3.38 (d, IH), 2.68 (t, IH), 2.55 (s, 3H), 2.18 (m, 3H), 1.62 (m, 4H), 0.90 (t, 3H), 0.63 (d, 3H), 0.36 (d, 3H); LC/MS m/z 523 (M + H)+
Figure imgf000092_0001
(±)-(c/>y,cώ)-3,5-Dimethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-70)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, cώ)-N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-68) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting ethyl chloroformate for 2-isocyanato-propane. *H ΝMR (300 MHz, CDC13) δ 8.77 (d, IH), 8.33 (m, 2H), 8.15 (s, IH), 7.94 (d, IH), 7.67 (m, 3H), 7.37 (m, 3H), 4.77 (d, IH), 4.07 (q, 2H), 3.75 (s, br, 2H), 3.48 (m, 2H), 2.58 (s, 3H), 2.37 (m, IH), 1.72 (m, 2H), 1.22 (t, 3H), 0.48 (s, br, 6H); LC/MS m/z 525 (M + H)+
Figure imgf000092_0002
(±)-(c/5,c 5)-3,5-DimethyI-4-[4-(2-methyl-benzoylamino)-naphthalene-l- su!fonylamino]-piperidine-l-carboxyIic acid dimethylamide (C-71)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, cis)- N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-68) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting dimethylcarbamyl chloride for 2-isocyanato- propane. 1H ΝMR (300 MHz, CDC13) δ 8.76 (d, IH), 8.26 (m, 3H), 7.95 (d, IH), 7.65 (m, 3H), 7.34 (m, 3H), 5.20 (d, IH), 3.51 (m, IH), 3.20 (d, 2H), 2.76 (s, 6H), 2.56 (s, 3H), 2.40 (t, 2H), 1.78 (m, 2H), 0.44 (dd, 6H); LC/MS m/z 524 (M + H)+
Figure imgf000093_0001
(±)-(c/-.,c s)-N-{4-[3,5-DimethyI-l-(piperidine-l-carbonyl)-piperidin-4- yIsulfamoyl]-naphthalen-l-yl}-2-methyI-benzamide (C-72) The title compound was made following general procedure in Scheme 5, substituting (±)-(cκ, cώ)- N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-68) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting piperidine-1 -carbonyl chloride for 2-isocyanato- propane. !H ΝMR (300 MHz, CDC13) δ 8.75 (d, IH), 8.33 (s, IH), 8.25 (m, TTT), 7.95 (d, IH), 7.63 (m, 3H), 7.32 (m, 3H), 5.08 (d, IH), 3.49 (d, IH), 3.18 (dd, 2H), 3.07 (s, br, 4H), 2.55 (s, 3H), 2.39 (t, TTT), 1.75 (m, 2H), 1.50 (s, br, 5H), 0.43 (dd, 6H); LC/MS m/z 564 (M + H)+
Figure imgf000093_0002
(±)-(cώ,cώ)-N-[4-(l-Acetyl-3,5-dimethyI-piperidin-4-ylsuIfamoyl)-naphthalen-l- yI]-2-methyl-benzamide (C-73)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cis, cώ)-N-[4-(3,5-dimethyl-piperidin-4-ylsulfamoyl)-naphthalen- 1 -yl]-2- methyl-benzamide (C-68) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-l) and substituting acetyl chloride for 2-isocyanato-propane. !H ΝMR (300 MHz, CDC13) δ 8.80 (d, IH), 8.28 (m, 3H), 7.76 (d, IH), 7.64 (m, 3H), 7.35 (m, 3H), 5.26 (d, IH), 4.16 (dd, IH), 3.51 (dd, IH), 3.32 (dd, IH), 3.32 (dd, IH), 2.74 (t, IH), 2.56 (s, 3H), 2.18 (t, IH), 1.99 (s, 3H), 1.70 (m, TTT), 0.60 (d, 3H), 0.38 (d, 3H); LC/MS m/z 495 (M + H)+
Figure imgf000094_0001
(±)-(c/5)-4-(l,3-Dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonic acid (3- methyl-piperidin-4-yl)-amide (C-74)
The title compound was made as its formate salt following general procedure in Scheme 4-2, substituting (±)-l-benzyl-3-methyl-piperidin-4-ylamine (1) for (±)-4- amino-l-benzyl-piperidine-3-carboxylic acid ethyl ester (6) and substituting 4-(l,3- dioxo-1, 3 -dihydro-isoindol-2-yl)-naphthalene-l -sulfonyl chloride for 4-(2-methyl- benzoylamino)-naphthalene-l -sulfonyl chloride. "H NMR (300 MHz, MeOD) δ 8.88 (d, IH), 8.45 (s, IH), 8.39 (d, IH), 8.02 (m, 2H), 7.93 (m, TTT), 7.80 (m, 2H), 7.67 (d, 2H), 3.50 (m, IH), 3.05 (m, 3H), 2.80 (t, IH), 1.95 (m, IH), 1.65 (m, TTT), 0.60 (d, 3H); LC/MS m/z 451 (M + H)+
Figure imgf000094_0002
(±)-(cώ)-4-(l,3-Dioxo-l,3-dihydro-isoindol-2-yl)-naphtha!ene-l-sulfonic acid (1- butyryl-3-methyl-piperidin-4-yl)-amide (C-75)
The title compound was made following general procedure in Scheme 5, substituting (±)-(cώ)-4-(l,3-dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonic acid (3- methyl-piperidin-4-yl)-amide (C-74) for N-[4-(piperidin-4-ylsulfamoyl)- naphthalen-1-yl] -benzamide (C-l) and substituting butyl chloride for 2-isocyanato- propane. 1H ΝMR (300 MHz, CDC13) δ 8.76 (dd, IH), 8.41 (dd, IH), 8.03 (dd, 2H), 7.88 (m, 2H), 7.74 (m, 2H), 7.58 (m, 2H), 5.25 (dd, IH), 3.30 (m, 4H), 2.22 (m, 2H), 1.65 (m, 6H), 0.90 (t, 3H), 0.70 (dd, 3H); LC/MS m/z 521 (M + H)+
Figure imgf000095_0001
(±)-(trflλis)-N-[4-(l-butyryI-3-hydroxymethyl-piperidin-4-ylsulfamoyl)- naphthalen-l-yl]-2-methyl-benzamide (C-76)
(±)-(trans)- 1 -Butyryl-4-[4-(2-methyl-benzoylamino)-naphthalene- 1 -sulfonylamino]- piperidine-3 -carboxylic acid ethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3-carboxylic acid ethyl ester (5) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting butyl chloride for 2-isocyanato-propane. To the solution of (±)-(tr rø)-l-butyryl-4- [4-(2-methyl-benzoylamino)-naphthalene- 1 -sulfonylamino] -piperidine-3 -carboxylic acid ethyl ester (121 mg, 0.21 mmol) in THF (5 mL), was added lithium borohydride in THF solution (1.07 mL, 2.1 mmol) and the resultant solution was stired at 0 °C for 2h. The solvent was removed in vacuo and the crude material was purified by HPLC to give the title compound. !H ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.32 (dd, IH), 8.24 (d, IH), 7.93 (d, IH), 7.70 (m, 3H), 7.38 (m, 3H), 4.00 (m, 3H), 3.20 (m, 2H), 2.88 (m, IH), 2.55 (s, 3H), 2.46 (m, IH), 2.28 (m, 2H), 1.50 (m, 3H), 1.24 (m, 2H), 0.90 (dd, 3H); LC/MS m/z 525 (M + H)+
Figure imgf000095_0002
(±)-(c/s)-4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-3-carboxyIic acid ethyl ester (C-77)
The title compound was prepared as its formate salt following general procedure in Scheme 4-2. 1H ΝMR (300 MHz, MeOD) δ 8.75 (d, IH), 8.52 (s, IH), 8.34 (d, IH), 8.25 (d, 3H), 7.97 (d, IH), 7.71 (m, 3H), 7.40 (m, 3H), 3.93 (m, IH), 3.70 (m, 2H), 3.28 (m, 2H), 3.07 (m, 2H), 2.90 (m, IH), 2.56 (s, 3H), 1.82 (m, 2H), 0.98 (t, 3H); LC/MS m/z 497 (M + H)+
Figure imgf000096_0001
(±)-(cw)-l-ButyryI-4-[4-(2-methyl-benzoylamino)-naphthalene-l- suIfony!amino]-piperidine-3-carboxylic acid (C-78)
(±)-(cώ)-l-Butyryl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-3 -carboxylic acid ethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting butyl chloride for 2-isocyanato-propane. To the solution of (±)-(cώ)-l-butyryl-4-[4- (2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-3-carboxylic acid ethyl ester (70 mg, 0.12 mmol) in THF (5 mL), was added lithium hydroxide in water solution (6 mg, 0.25 mmol) and the resultant solution was stired at 25 °C for 2h. The reaction mixture was extracted with CH2C12. The organic extracts were washed with brine, dried over Na2S0 , filtered and concentrated to provide the crude product. HPLC purification of the residue gave the title compound. *H NMR (300 MHz, DMSO) δ 10.62 (s, IH), 8.77 (t, IH), 8.24 (m, 3H), 7.95 (d, IH), 7.70 (m,
3H), 7.38 (m, 3H), 3.72 (m, 2H), 3.35 (m, 6H), 3.12 (m, IH), 2.60 (m, IH), 2.15 (m, 2H), 1.32 (m, 4H), 0.80 (dd, 3H); LC/MS m/z 539 (M + H)+
Figure imgf000096_0002
(±)-(tr««s)-4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-l,3-dicarboxylic acid diethyl ester (C-79)
The title compound was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3-carboxylic acid ethyl ester (5) for 4-aminopiperidine-l -carboxylic acid tert-butyl ester and substituting ethyl chloroformate for 2-isocyanato-propane. 'H NMR (300 MHz, MeOD) δ 8.68 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.93 (d, IH), 7.70 (m, 3H), 7.38 (m, 3H), 4.00 (m, 4H), 3.48 (m, 3H), 2.85 (m, 2H), 2.55 (s, 3H), 2.36 (dt, IH), 1.75 (d, IH), 1.32 (d, IH), 1.21 (t, 3H), 0.96 (t, 3H); LC/MS m/z 568 (M + H)+
Figure imgf000097_0001
(±)-(c s)-N-[4-(l-Butyryl-3-hydroxymethyl-piperidin-4-yIsulfamoyl)- naphthalen-l-yl]-2-methyI-benzamide (C-80)
(±)-(cis)-l -Butyryl-4- [4-(2-methyl-benzoylamino)-naphthalene- 1 -sulfonylamino] - piperidine-3 -carboxylic acid ethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting butyl chloride for 2-isocyanato-propane. To the solution of (±)-(cis)-l -butyryl-4- [4- (2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-3-carboxylic acid ethyl ester (48 mg, 0.085 mmol) in THF (5 mL), was added lithium borohydride in THF solution (0.5 mL, 0.25 mmol) and the resultant solution was stired at 0 °C for 2h. The solvent was removed in vacuo and the crude material was purified by HPLC to give the title compound. 1H ΝMR (300 MHz, MeOD) δ 8.81 (d, IH), 8.34 (d, IH), 8.25 (d, IH), 7.95 (d, IH), 7.72 (m, 3H), 7.40 (m, 3H), 3.46 (m, 7H), 2.56 (s, 3H), 2.32 (m, 2H), 2.55 (s, 3H), 1.52 (m, 5H), 0.92 (m, 3H); LC/MS m/z 525 (M + H)+
Figure imgf000097_0002
(±)-(c-,s)-3-Hydroxymethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-81)
(±)-(cw)-4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine- 1,3-dicarboxylic acid diethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and substituting ethyl chloroformate for 2-isocyanato-propane. To the solution of (±)-(cώ)- 4-[4-(2- Methyl-benzoylamino)-naphthalene- 1 -sulfonylamino] -piperidine- 1 ,3 -dicarboxylic acid diethyl ester (57 mg, 0.1 mmol) in THF (5 mL), was added lithium borohydride in THF solution (0.5 mL, 0.25 mmol) and the resultant solution was stired at 0 °C for 2h. The solvent was removed in vacuo and the crude material was purified by HPLC to give the title compound. 'H NMR (300 MHz, MeOD) δ 8.81 (d, IH), 8.33 (d, IH), 8.24 (d, IH), 7.94 (d, IH), 7.72 (m, 3H), 7.40 (m, 3H), 4.06 (q, 2H), 3.55 (m, 2H), 3.32 (m, 5H), 2.56 (s, 3H), 1.75 (m, IH), 1.30 (m, 2H), 1.20 (t, 3H); LC/MS m/z 526 (M + H)+
Figure imgf000098_0001
(±)-(tra«s)-3-Hydroxymethyl-4-[4-(2-methyl-benzoyIamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-82)
(±)-(trα«5)-4-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-l,3-dicarboxylic acid diethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting ethyl chloroformate for 2-isocyanato-propane. To the solution of (±)-(trans)- 4- [4- (2-methyl-benzoylamino)-naphthalene- 1 -sulfonylamino] -piperidine- 1 ,3 -dicarboxylic acid diethyl ester (57 mg, 0.1 mmol) in THF (5 mL), was added lithium borohydride in THF solution (0.5 mL, 0.25 mmol) and the resultant solution was stired at 0 °C for 2h. The solvent was removed in vacuo and the crude material was purified by HPLC to give the title compound. 'H NMR (300 MHz, MeOD) δ 8.73 (d, IH), 8.30 (d, IH), 8.22 (d, IH), 7.93 (d, IH), 7.68 (m, 3H), 7.36 (m, 3H), 4.15 (d, IH), 4.05 (q, 2H), 3.85 (d, IH), 3.55 (d, IH), 3.25 (m, IH), 3.10 (m, IH), 2.60 (m, TTT), 2.56 (s, 3H), 1.40 (m, 3H), 1.20 (t, 3H); LC/MS m/z 526 (M + H)+
Figure imgf000099_0001
l-(2-DimethyIamino-acetyl)-4-[4-(2-methyl-benzoyIamino)-naphthalene-l- sulfonylamino]-piperidine-3-carboxy!ic acid ethyl ester (C-83)
The title compound was made following general procedure in Scheme 5, substituting (±)-4-amino-l-benzyl-piperidine-3 -carboxylic acid ethyl ester (5) for 4-aminopiperidine-l -carboxylic acid tert-butyl ester and substituting dimethylamino-acetyl chloride hydrochloride for 2-isocyanato-propane. !H NMR (300 MHz, CDC13) δ 8.62 (m, IH), 8.32 (m, 3H), 7.94 (d, IH), 7.64 (m, 3H), 7.36 (m, 3H), 5.95 (m, IH), 4.10 (m, 4H), 3.50 (s, br, IH), 3.05 (m, 6H), 2.56 (m, 3H), 2.25 (dd, 6H), 1.84 (m, IH), 1.10 (m, 3H); LC/MS m/z 581 (M + H)+
Figure imgf000099_0002
(±)-(cώ)-3-Ethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfony!amino]- piperidine-l-carboxylic acid ethyl ester (C-84) The title compound was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting ethyl chloroformate for 2-isocyanato-propane. *H NMR (300 MHz, CDC13) δ 8.71 (d, IH), 8.37 (m, 2H), 8.13 (s, IH), 7.93 (d, IH), 7.66 (m, 3H), 7.43 (m, IH), 7.33 (m, 2H), 4.78 (d, IH), 4.05 (m, 2H), 3.42 (m, IH), 3.22 (m, 4H), 2.58 (s, 3H), 1.35 (s, br, 2H), 1.17 (t, 3H), 1.00 (s, br, 2H), 0.55 (s, br, 3H); LC/MS m/z 524 (M + H)+
Figure imgf000100_0001
(±)-(cw)-N-[4-(l-Butyryl-3-ethyl-piperidin-4-ylsulfamoyI)-naphthalen-l-yI]-2- methyl-benzamide (C-85)
The title compound was made following general procedure in Scheme 5, substituting (±)-l -benzyl-3 -ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and substituting butyl chloride for 2-isocyanato-propane. !H ΝMR (300 MHz, CDC13) δ 8.72 (d, IH), 8.37 (m, 2H), 8.16 (s, IH), 7.94 (d, IH), 7.66 (m, 3H), 7.43 (m, IH), 7.33 (m, 2H), 4.90 (m, IH), 3.32 (m, 5H), 2.58 (s, 3H), 2.18 (m, 2H), 1.45 (m, 6H), 0.87 (t, 3H), 0.50 (m, 3H); LC/MS m/z 522 (M + H)+
Figure imgf000100_0002
(±)-(c/,s)-3-Ethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid dimethylamide (C-86)
The title compound was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and substituting dimethylamino-acetyl chloride hydrochloride for 2-isocyanato-propane. 'H ΝMR (300 MHz, CDC13) δ 8.72 (d, IH), 8.36 (m, 2H), 8.16 (s, IH), 7.93 (d, IH), 7.65 (m, 3H), 7.42 (m, IH), 7.32 (m, 2H), 4.88 (d, IH), 3.45 (m, IH), 3.20 (m, IH), 3.00 (m, 2H), 2.80 (m, IH), 2.70 (s, 6H), 2.50 (s, 3H), 1.40 (m, 3H), 1.00 (m, 2H), 0.52 (t, 3H); LC/MS m/z 523 (M + H)+
Figure imgf000100_0003
(±)-(tra«s)-3-Ethyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-87) The title compound was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and substituting ethyl chloroformate for 2-isocyanato-propane. 1H NMR (300 MHz, CDC13) δ 8.69 (d, IH), 8.36 (m, 2H), 8.12 (s, IH), 7.93 (d, IH), 7.66 (m, 3H), 7.43 (m, IH), 7.33 (m, 2H), 4.50 (d, IH), 4.05 (m, 2H), 3.55 (d, IH), 2.95 (m, IH), 2.70 (t, IH), 2.57 (s, 3H), 2.49 (m, IH), 1.50 (m, 3H), 1.17 (m, 5H), 0.85 (m, IH), 0.65 (s, br, 3H); LC/MS m/z 524 (M + H)+
Figure imgf000101_0001
(±)-(tra j5,)-N-[4-(l-Butyryl-3-ethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-88)
The title compound was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting butyl chloride for 2-isocyanato-propane. *H ΝMR (300 MHz, CDC13) δ 8.68 (m, IH), 8.35 (m, 2H), 8.18 (s, IH), 7.94 (d, IH), 7.66 (m, 3H), 7.42 (m, IH), 7.32 (m, TTT), 4.65 (d, IH), 4.30 (m, IH), 3.68 (m, IH), 2.95 (m, 2H), 2.57 (s, 3H), 2.50 (m, IH), 2.20 (m, 2H), 1.55 (m, 5H), 1.15 (m, 2H), 0.85 (t, 3H), 0.60 (m, 3H); LC/MS m/z 522 (M + H)+
Figure imgf000101_0002
ylsulfamoyl]-naphthaIen-l-yI}-2-methyl-benzamide (C-89) The title compound was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and substituting 3-methyl-3H-imidazole-4-carbonyl chloride hydrochloride for 2-isocyanato-propane. !H NMR (300 MHz, MeOD) δ 8.79 (d, IH), 8.33 (d, IH), 8.25 (d, IH), 8.15 (s, IH), 7.94 (d, IH), 7.70 (m, 4H), 7.43 (m, IH), 7.36 (m, 2H), 7.14 (s, IH), 4.20 (m, 2H), 3.75 (s, 3H), 3.05 (m, 2H), 2.70 (m, IH), 2.55 (s, 3H), 1.55 (m, 3H), 1.30 (m, IH), 0.85 (m, IH), 0.62 (m, 3H); LC/MS m/z 560 (M + H)+
Figure imgf000102_0001
(±)-(cw)-N-{4-[l-(2-Dimethylamino-acetyl)-3-ethyl-piperidin-4-ylsulfamoyl]- naphthalen-l-yI}-2-methyl-benzamide (C-90)
The title compound (formic acid salt) was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-amino- piperidine- 1 -carboxylic acid tert-butyl ester, and substituting dimethylamino-acetyl chloride hydrochloride for 2-isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.85 (d, TTT), 8.55 (s, IH), 8.32 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH), 7.35 (m, TTT), 3.47 (m, ATT), 3.25 (m, 2H), 2.55 (s, 3H), 2.33 (d, 6H), 1.38 (m, 3H), 1.15 (m, 3H), 0.50 (m, 3H); LC/MS m/z 537 (M + H)+
Figure imgf000102_0002
(±)-(trαn*)--V-{4-[l-(2-Dimethylamino-acetyl)-3-ethyl-piperidin-4-yIsulfamoyI]- naphthalen-l-yl}-2-methyI-benzamide (C-91) The title compound (formic acid salt) was made following general procedure in Scheme 5, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for 4-aminopiperidine-l -carboxylic acid tert-butyl ester and substituting dimethylamino-acetyl chloride hydrochloride for 2-isocyanato-propane. !H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.55 (s, IH), 8.32 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH), 7.35 (m, 2H), 4.05 (m, 2H), 3.10 (m, 3H), 2.60 (m, IH), 2.55 (s, 3H), 2.30 (s, 6H), 1.25 (m, 2H), 1.10 (m, 3H), 0.90 (m, IH), 0.85 (m, 3H); LC/MS m/z 537 (M + H)+
Figure imgf000103_0001
(3R, 4R)-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxyIic acid ethyl ester (C-92)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3R, R)-4-amino-3 -methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and ethyl chloroformate for 2-isocyanato-propane. lK NMR (300 MHz, CDC13) δ 8.77 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.92 (d, IH), 7.73 (m, 3H), 7.35 (m, 3H), 4.03 (q, 2H), 3.94 (t, 2H), 2.85 (dt, IH), 2.64 (m, IH), 2.55 (s, 3H), 2.40 (m, IH), 1.48 (m, IH), 1.38 (m, IH), 1.20 (t, 3H), 0.59 (d, 3H); LC/MS m/z 510 (M + H)+.
Figure imgf000103_0002
(3S, ^S)-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (C-93)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3S, S)-4-amino-3 -methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and ethyl chloroformate for 2-isocyanato-propane. !H NMR (300 MHz, CDC13) δ 8.77 (d, IH), 8.30 (d, IH), 8.23 (d, IH), 7.92 (d, IH), 7.73 (m, 3H), 7.35 (m, 3H), 4.03 (q, 2H), 3.94 (t, TTT), 2.85 (dt, IH), 2.64 (m, IH), 2.55 (s, 3H), 2.40 (m, IH), 1.48 (m, IH), 1.38 (m, IH), 1.20 (t, 3H), 0.59 (d, 3H); LC/MS m/z 510 (M + H)+.
Figure imgf000104_0001
(3R, ^-R)-2-Methyl-N-[4-(3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- benzamide (C-94)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3R, R)-4-amino-3 -methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 'H ΝMR (300 MHz, MeOD) δ 8.78 (dd, IH), 8.34 (d, IH), 8.24 (dd, IH), 7.94 (d, IH), 7.78 (m, IH), 7.74 (m, IH), 7.69 (m, IH), 7.44 (m, IH), 7.37 (m, TTT), 3.23 (m, 2H), 3.00 (m, IH), 2.78 (m, IH), 2.64 (m, IH), 2.55 (s, 3H), 1.76 (m, 2H), 1.58 (m, IH), 0.66 (d, 3H); LC/MS m/z 438 (M + H)+.
Figure imgf000104_0002
(3S, ^S)-2-Methyl-N-[4-(3-methyl-piperidin-4-ylsulfamoyl)-naphthaIen-l-yl]- benzamide (C-95)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3S, S)-4-amino-3 -methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. !H ΝMR (300 MHz, MeOD) δ 8.78 (dd, IH), 8.34 (d, IH), 8.24 (dd, IH), 7.94 (d, IH), 7.78 (m, IH), 7.74 (m, IH), 7.69 (m, IH), 7.44 (m, IH), 7.37 (m, 2H), 3.23 (m, 2H), 3.00 (m, IH), 2.78 (m, IH), 2.64 (m, IH), 2.55 (s, 3H), 1.76 (m, 2H), 1.58 (m, IH), 0.66 (d, 3H); LC/MS m/z 438 (M + H)+.
Figure imgf000105_0001
(3S, Sj-N-[4-(l-Butyryl-3-methyl-piperidin-4-ylsuIfamoyI)-naphthalen-l-yl]-2- methyl-benzamide (C-96)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3S, ¥S)-4-amino-3 -methyl-piperidine- 1 -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and butyryl chloride for 2- isocyanato-propane. *HΝMR (300 MHz, CDC13) δ 8.70 (t, IH), 8.33 (m, 3H), 7.95 (d, IH), 7.62 (m, 3H), 7.40 (m, IH), 7.34 (m, TTT), 5.00 (d, IH), 4.30 (dd, TTT), 3.63 (m, IH), 2.85 (m, 1.5H), 2.57 (s, 3H), 2.40 (t, 0.5H), 2.15 (m, 1.5H), 2.09 (m, 0.5H), 1.83 (m, 0.5H), 1.50 (m, 1.5H); LC/MS m/z 508 (M + H)+.
Figure imgf000105_0002
(3R, ^R)-N-[4-(l-Butyryl-3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-97)
The title compound was prepared according to the general procedure in Scheme 5, substituting (3R, R)-4-amino-3-methyl-piperidine-l-carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester, and butyiyl chloride for 2- isocyanato-propane. 1HΝMR (300 MHz, CDC13) δ 8.70 (t, IH), 8.33 (m, 3H), 7.95 (d, IH), 7.62 (m, 3H), 7.40 (m, IH), 7.34 (m, 2H), 5.00 (d, IH), 4.30 (dd, IH), 3.63 (m, IH), 2.85 (m, 1.5H), 2.57 (s, 3H), 2.40 (t, 0.5H), 2.15 (m, 1.5H), 2.09 (m, 0.5H), 1.83 (m, 0.5H), 1.50 (m, 1.5H); LC/MS m/z 508 (M + H)+.
Figure imgf000106_0001
4-[4-(l,3-Dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid ethylamide (C-98)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(l,3-dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonyl chloride, and substituting ethyl isocyanate for 2-isocyanato-propane. 1H NMR (300 MHz, DMSO) δ 8.75 (d, IH), 8.29 (d, IH), 8.23 (d, IH), 8.03 (m, 5H), 7.83 (d, IH), 7.80 (t, IH), 7.67 (t, IH), 6.36 (t, IH), 3.69 (d, 2H), 3.27 (m, IH), 2.97 (p, 2H), 2.64 (t, 2H), 1.47 (d, 2H), 1.23 (m, 2H), 0.95 (t, 3H); LC/MS m/z 505 (M - H .
Figure imgf000106_0002
2-Fluoro-N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-99)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-fluoro-benzoylamino)-naphthalene-l -sulfonyl chloride. 1H ΝMR (300 MHz, DMSO) δ 10.72 (s, IH), 8.67 (d, IH), 8.30 (d, IH), 8.20 (d, IH), 8.10 (d, IH), 8.01 (d, IH), 7.83 (t, IH), 7.74 (t, 2H), 7.65 (m, IH), 7.41 (q, 2H), 3.67 (d, 2H), 3.18 (m, IH), 2.70 (m, 2H), 1.43 (m, 2H), 1.18(m, 2H); LC/MS m/z 426 (M - H)- , 428 (M + H)+
Figure imgf000107_0001
4-[4-(2-Fluoro-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethylamide (C-100)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-fluoro-benzoylamino)-naphthalene-l -sulfonyl chloride, and substituting ethyl isocyanate for 2-isocyanato-propane. *H NMR (300 MHz, DMSO) δ 10.74 (s, IH), 8.67 (d, IH), 8.29 (d, IH), 8.19 (d, IH), 8.05 (d, IH), 7.99 (d, IH), 7.82 (t, IH), 7.73 (t, 2H), 7.65 (t, 2H), 7.41 (q, 2H), 6.32 (t, IH), 3.67 (d, 2H), 3.17 (m, IH), 2.94 (m, 2H), 2.59 (t, 2H), 1.36 (d, 2H), 1.14 (m, 2H), 0.95 (t, 3H); /MS m/z 498 (M - H)', 500 (M + H)+
Figure imgf000107_0002
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yI]-2-trifluoromethyl- benzamide (C-101)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-trifluoromethyl-benzoylamino)-naphthalene-l -sulfonyl chloride and substituting butyryl chloride and triethylamine for 2-isocyanato-propane. 1H ΝMR (300 MHz, DMSO) δ 10.91(s, IH), 8.68 (d, IH), 8.25 (m, 2H), 8.11 (d, IH), 7.85 (m, 4H), 7.76 (m, 3H), 4.06 (m, IH), 4.0 l(m, IH), 3.62 (d, IH), 2.94 (t, IH), 2.59 (t, 2H), 1.48 (m, 2H), 1.41 (m, 2H), 1.19 (m, 2H), 0.82 (t, 3H); LC/MS m/z 546 (M - HT, 548 (M + H)+
Figure imgf000108_0001
2-Methoxy-N-[4-(l-propionyl-piperidin-4-ylsulfamoyI)-naphthaIen-l-yl]- benzamide (C-102)
The title compound was prepared following the general procedure in Scheme 5 beginning with 4-(2-methoxy-benzoylamino)-naphthalene-l -sulfonyl chloride, and substituting propionyl chloride and triethylamine for 2-isocyanato-propane. LC/MS m/z 495 (M - H)_ , 497 (M + H)+
Figure imgf000108_0002
2-Chloro-N-[4-(l-propionyl-piperidin-4-ylsulfamoyl)-naphthaIen-l-yl]- benzamide (C-103)
The title compound was prepared following the general procedure in Scheme 5 beginning with 4-(2-chloro-benzoylamino)-naphthalene-l -sulfonyl chloride, and substituting propionyl chloride and triethylamine for 2-isocyanato-propane. !H ΝMR (300 MHz, DMSO) δ 10.86 (s, IH), 8.68 (d, IH), 8.33 (d, TTT), 8.22 (d, IH), 8.12 (d, IH), 7.98 (d, IH), 7.74 (m, 3H), 7.64 (t, IH), 7.54 (m, 2H), 4.01 (m, IH), 3.59 (d, IH), 3.24 (m, IH), 3.16 (d, IH), 2.96 (t, IH), 2.20 (q, 2H), 1.51 (d, 2H), 1.20 (m, 2H), 0.81 (t, 3H); LC/MS m/z 498 (M - HV, 500 (M + H)+
Figure imgf000108_0003
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methoxy- benzamide (C-104) The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-methoxy-benzoylamino)-naphthalene-l -sulfonyl chloride, and substituting butyric chloride and triethylamine for 2-isocyanato-propane. LC/MS m/z 508 (M - TT)', 510 (M + H)+
Figure imgf000109_0001
N-[4-(l-Butyryl-piperidin-4-ylsuIfamoyl)-naphthalen-l-yl]-2-chloro-benzamide
(C-105)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-chloro-benzoylamino)-naphthalene- 1 -sulfonyl chloride, and substituting butyryl chloride and triethylamine for 2-isocyanato-propane. "H ΝMR (300 MHz, DMSO) δ 10.86 (s, IH), 8.68 (d, IH), 8.35 (d,lH), D D D(d,lH), 8.13 (d, IH), 8.0 (m, IH), 7.74 (m, 3H), 7.64 (m, 3H), 4.00 (d, IH), 3.60 (d, IH), 3.26 (m, IH), 2.93 (t, IH), 2.59 (m, 2H), 2.17 (t, 2H), 1.46 (m, 2H), 1.43 (q, TTT), 1.17 (m, IH), 0.82 (t, 3H); LC/MS m/z 512 (M - H)_, 514 (M + H)+
Figure imgf000109_0002
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-fluoro-benzamide (C-106) The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-fluoro-benzoylamino)-naphthalene-l -sulfonyl chloride and substituting butyryl chloride and triethylamine for 2-isocyanato-propane. Η ΝMR (300 MHz, DMSO) δ 10.73 (s, IH), 8.69 (d, IH), 8.28 (d, IH), 8.21 (d, IH), 8.11 (d, IH), 7.99 (d, IH), 7.83 (t, IH), 7.76 (m, TTT), 7.64 (m, IH), 7.40 (q, 2H), 4.00 (d, IH), D.60 (d, IH), 3.26 (m, IH), 2.93 (t, IH), 2.59 (m, 2H), 2.17 (t, 2H), 1.46 (m, 2H), 1.43 (q, 2H), 1.17 (m, IH), 0.82 (t, 3H); LC/MS m/z 496 (M - HV, 498 (M + H)+
Figure imgf000110_0001
2-Fluoro-N-[4-(piperidin-4-ylsuIfamoyl)-naphthalen-l-yl]-6-trifluoromethyl- benzamide (C-107)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-fluoro-6-trifluoromethyl-benzoylamino)-naphthalene- 1 -sulfonyl chloride. Η ΝMR (300 MHz, DMSO) δ 11.15 (s, IH), 8.70 (d, IH), 8.32 (d, TTT), 8.29 (m, IH), 8.01 (d, IH), 7.77 (m, IH), 7.65 (m, IH), 7.32 (m, IH), 6.94 (m, IH), 3.08 (d, IH), 2.85 (m, IH), 2.54 (m, 5H), 1.64 (m, IH), 1.51 (m, IH). LC/MS m/z 494 (M - HT, 496 (M + H)+
Figure imgf000110_0002
2,6-Difluoro-N-[4-(piperidin-4-ylsuIfamoyl)-naphthalen-l-yI]-benzamide (C- 108)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2,6-difluoro-benzoylamino)-naphthalene-l -sulfonyl chloride. *H ΝMR (300 MHz, DMSO) δ 11.15 (s, IH), 8.70 (d, IH), 8.32 (d, IH), 8.29 (m, IH), 8.01 (d, IH), 7.77 (m, IH), 7.65 (m, IH), 7.32 (m, IH), 6.94 (m, IH), 3.08 (d, IH), 2.85 (m, IH), 2.54 (m, 5H), 1.64 (m, IH), 1.51 (m, IH). LC/MS m/z 444 (M - H)\ 446 (M + H)+
Figure imgf000110_0003
N-[4-(l-ButyryI-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2,6-difluoro- benzamide (C-109)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2,6-difluoro-benzoylamino)-naphthalene-l -sulfonyl chloride, and substituting butyryl chloride and triethylamine for 2-isocyanato-propane. 'H ΝMR (300 MHz, DMSO) δ 11.12(s, IH), 8.71 (m, IH), 8.26 (m, 2H), 8.13 (d, IH), 7.98 (d, IH), 7.75 (m, 2H), 7.62 (m, IH), 7.31 (t, 2H), 4.01 (d, IH), 3.60 (d, IH), 2.93 (t, IH), 2.59 (m, TTT), 2.15 (t, 2H), 1.45 (m, 2H), 1.43 (q, 2H), 1.17 (m, 2H), 0.81 (t, 3H); LC/MS m/z 514 (M - HV, 516 (M + H)+
Figure imgf000111_0001
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-fluoro-6- trifluoromethyl-benzamide (C-l 10)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2-fluoro-6-trifluoromethyl-benzoylamino)-naphthalene- 1 -sulfonyl chloride and substituting butyric chloride and triethylamine for 2-isocyanato- propane. 1H ΝMR (300 MHz, DMSO) δ 11.12 (s, IH), 8.71 (m, IH), 8.26 (m, TTT), 8.13 (m, IH), 7.98 (d, IH), 7.79 (m, 6H), 4.01 (d, IH), 3.60 (d, IH), 2.93 (t, IH), 2.59 (m, 2H), 2.15 (t, 2H), 1.45 (m, 2H), 1.43 (q, 2H), 1.17 (m, 2H), 0.81 (t, 3H). LC/MS m/z 514 (M - HV, 516 (M + H)+
Figure imgf000111_0002
N-[4-(l-Butyryl-piperidin-4-ylsuIfamoyl)-naphthaIen-l-yI]-2,4-dichloro- benzamide (C-l 11) The title compound was prepared following the general procedure in Scheme 5, beginning with 4-(2,4-dichloro-benzoylamino)-naphthalene-l -sulfonyl chloride and substituting butyryl chloride and triethylamine for 2-isocyanato-propane. lH NMR (300 MHz, DMSO) δ 10.87 (s, IH), 8.70 (dd, IH), 8.34 (dd, IH), 8.21 (d, IH), 8.13 (d, IH), 8.01 (d, IH), 7.82 (m, 2H), 7.73 (m, IH), 7.63 (d, IH), 4.00 (d, IH), 3.6 (d, IH), 3.24 (m, IH), 2.92 (t, IH), 2.59 (m, IH), 2.17 (t, 2H), 1.47 (m, 2H), 1.43 (m, 2H), 1.18 (m, TTT), 0.82 (t, 3H). LC/MS m/z 548 (M - TT); 560 (M + H)+
Figure imgf000112_0001
(±)-2-MethyI-N-[4-(piperidin-3-ylsuIfamoyl)-naphthalen-l-yl]-benzamide (C- 112) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and 3-amino-piperidine-l -carboxylic acid tert- butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, 2H), 8.25 (d, IH), 7.96 (d, IH), 7.71 (m, 3H), 7.45 (m, IH ), 7.38 (m, 2H), 3.33 (m, IH), 3.19 (m, 2H), 2.70 (m, 2H), 2.57 (s, 3H), 1.83 (m, IH), 1.55 (m, 3H); LC/MS (M + H)+ m/z 424.
Figure imgf000112_0002
(±)-3-[4-(2-MethyI-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethylamide (C-l 13)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene- 1 -sulfonyl chloride, 3-amino-piperidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and isocyanato-ethane for 2-isocyanato-propane. 'HΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (m, 2H), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, TTT), 3.79 (m, IH), 3.55 (m, IH), 3.12 (q, 2H), 3.10 (m, IH ), 2.85 (m, IH), 2.72 (m, IH), 2.55 (s, 3H), 1.58 (m, 2H), 1.30 (m, 2H), 1.19 (m, 3H); LC/MS (M + H)+ m/z 495.
Figure imgf000113_0001
(±)-N-[4-(l-Butyryl-piperidin-3-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-114)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 3-amino-piperidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and butyryl chloride for 2-isocyanato-propane. 1H ΝMR (300 MHz, MeOD) δ 8.78 (m, IH), 8.33 (m, 2H), 8.23 (m, IH), 7.94 (m, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 3.79 (m, IH), 3.91 (m, IH), 3.55 (q, IH), 3.08 (m, IH ), 2.95 (m, IH), 2.82 (m, IH), 2.55 (s, 3H), 2.01 (m, 2H), 1.50 (m, 6H), 0.90 (m, 3H); LC/MS (M + H)+ m/z 494.
Figure imgf000113_0002
(±)-3-[4-(2-Methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (C-115)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 3-amino-piperidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl chlorofomate for 2-isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (m, IH), 8.33 (m, 2H), 8.23 (m, IH), 7.94 (m, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.02 (m, 2H), 3.70 (m, 2H), 3.06 (m, IH), 2.69 (m, IH ), 2.38 (m, IH), 2.55 (s, 3H), 1.71 (m, 2H), 1.30 (m, 2H), 1.18 (m, 3H); LC/MS (M + H)+ m/z 496.
Figure imgf000114_0001
2-Methyl-N-{4-[(piperidin-4-yImethyl)-sulfamoyl]-naphthaIen-l-yl}-benzamide (C-116)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, and 4-aminomethyl-piperidine-l -carboxylic acid tert-butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. *H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.29 (m, TTT), 7.93 (m, IH), 7.74 (m, 3H), 7.41 (m, 3H ), 3.30 (m, TTT), 2.82 (m, 2H), 2.80 (d, 2H), 2.55 (s, 3H), 1.84 (m, 2H), 1.65 (m, IH), 1.28 (m, 2H); LC/MS (M + H)+ m/z 438.
Figure imgf000114_0002
4-{[4-(2-Methyl-benzoylamino)-naphthalene-l-suIfonyIamino]-methyl}- piperidine-1-carboxylic acid ethylamide (C-l 17) The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 4-aminomethyl-piperidine-l -carboxylic acid tert- butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and isocyanato- ethane for 2-isocyanato-propane. 'H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.29 (m, 2H), 7.93 (m, IH), 7.74 (m, 3H), 7.41 (m, 3H ), 3.79 (m, 2H), 3.25 (q, 2H), 2.78 (d, TTT), 2.61 (m, TTT), 2.57 (s, 3H), 1.56 (m, 3H), 1.09 (t, 3H), 0.92 (m, 2H); LC/MS (M + H)+ m/z 509.
Figure imgf000115_0001
N-{4-[(l-Butyryl-piperidin-4-ylmethyl)-sulfamoyl]-naphthalen-l-yl}-2-methyl- benzamide (C-l 18)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 4-aminomethyl-piperidine-l -carboxylic acid tert- butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and butyryl chloride for 2-isocyanato-propane. *H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.29 (m, 2H), 7.93 (m, IH), 7.74 (m, 3H), 7.41 (m, 3H ), 4.49 (m, IH), 3.85 (m, IH), 2.89 (m, IH), 2.78 (d, 2H), 2.57 (s, 3H), 2.41 (m, IH), 2.30 (t, 2H), 1.61 (m, 5H), 0.96 (t, 3H), 0.93 (m, 2H); LC/MS (M + H)+ m/z 508.
Figure imgf000115_0002
4-{[4-(2-Methyl-benzoyIamino)-naphthalene-l-sulfonylamino]-methyl}- piperidine-1-carboxylic acid ethyl ester (C-l 19)
The title compound was made following general procedure in Scheme 5, substituting 4-(2-methyl-benzoylamino)-naphthalene-l -sulfonyl chloride for 4-benzoylamino- naphthalene-l -sulfonyl chloride, 4-aminomethyl-piperidine-l -carboxylic acid tert- butyl ester for 4-amino-piperidine-l -carboxylic acid tert-butyl ester and ethyl chlorofomate for 2-isocyanato-propane. !H ΝMR (300 MHz, MeOD) δ 8.78 (d,
IH), 8.29 (m, 2H), 7.93 (m, IH), 7.74 (m, 3H), 7.41 (m, 3H ), 4.09 (q, 2H), 4.00 (m, 2H), 2.78 (d, 2H), 2.59 (m, 2H), 2.57 (s, 3H), 1.59 (m, 3H), 1.22 (t, 3H), 0.90 (m, 2H); LC/MS (M + H)+ m/z 510.
Scheme 6
Figure imgf000116_0001
Deprotection in scheme 4 *.
Figure imgf000116_0002
Figure imgf000116_0003
4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (15)
The title compound was prepared following the general procedure in Scheme 2, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for/ anisidine and 2-methylbenzoyl chloride for benzoyl chloride. LC/MS (M + H)+ m/z 524.
Figure imgf000116_0004
(S)-N-{4-[l-(2-Amino-propionyl)-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}-2- methyl-benzamide (C-120)
2-Methyl-N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-36) was prepared from 4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester 15 via coupling and deprotection as shown in Scheme 4-1. To a 25 °C mixture of 2-methyl-N-[4-(piperidin-4- ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-36) hydrochloride (368 mg, 0.8 mmol) in CH2C12 (12 mL), was added 1-hydroxybenzotriazole hydrate (108 mg, 0.8 mmol), l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (184 mg, 0.96 mmol), N-methylmorpholine (243 mg, 2.4 mmol) and (S)-2-tert- butoxycarbonylamino-propionic acid. After stirring at 25 °C for 20 hours, the reaction mixture was filtered and the filtrate was concentrated to dryness in vacuo to afford 16. A solution of 4Ν HCl/Dioxane (5 mL) was added and the mixture was stirred for 2 hours. After removing the solvent, the crude product was purified via chromatography. 1H NMR (300 MHz, MeOD) δ 8.71 (d, IH), 8.28 (m, 3H), 7.96 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.00 (m, 2H), 3.60 (m, 2H), 3.01 (m, IH ), 2.71 (m, TTT), 2.49 (s, 3H), 1.57 (m, 2H), 1.22 (m, TTT), 1.09 (m, 3H); LC/MS (M + H)+ m/z 495.
Figure imgf000117_0001
N-{4-[l-(2-Hydroxy-acetyl)-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}-2- methyl-benzamide (C-121) The title compound was made following general procedure in Scheme 6, substituting hydroxy-acetic acid for (S)-2-tert-butoxycarbonylamino-propionic acid. !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.33 (d, IH), 8.23 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.16 (m, IH), 4.13 (s, 2H), 3.55 (m, IH), 3.34 (m, IH), 2.95 (m, IH ), 2.74 (m, IH), 2.55 (s, 3H), 1.63 (m, 2H), 1.41 (m, 2H); LC/MS (M + H)+ m/-r 483.
Figure imgf000117_0002
N-{4-[l-(2-Amino-acetyl)-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}-2-methyI- benzamide (C-122) The title compound was made following general procedure in' Scheme 6, substituting tert-butoxycarbonylamino-acetic acid for (S)-2-tert-butoxycarbonylamino-propionic acid. 1H ΝMR (300 MHz, MeOD) δ 8.72 (d, TTT), 8.25 (m, 3H), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.05 (m, IH), 3.60 (m, 4H), 2.95 (m, IH ), 2.74 (m, IH), 2.49 (s, 3H), 1.55 (m, TTT), 1.31 (m, 2H); LC/MS (M + H)+ m/z 481.
Figure imgf000117_0003
(S)-2-Methyl-N-{4-[l-(2-methylamino-propionyl)-piperidin-4-ylsulfamoyI]- naphthalen-l-yI}-benzamide (C-123) The title compound was made following general procedure in Scheme 6, substituting (ιS)-2-(tert-butoxycarbonyl-methyl-amino)-propionic acid for (S)-2-tert- butoxycarbonylamino-propionic acid. !H NMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.25 (m, 3H), 7.96 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.10 (m, IH), 3.60 (m, 2H), 3.01 (m, IH), 2.71 (m, IH), 2.49 (s, 3H), 2.19 (d, 3H), 1.57 (m, 2H), 1.22 (m, 2H), 1.05 (m, 3H); LC/MS (M + H)+ m/z 509.
Figure imgf000118_0001
(S)-2-Methyl-N-{4-[l-(l-methyl-pyrrolidine-2-carbonyl)-piperidin-4- ylsulfamoyl]-naphthaIen-l-yl}-benzamide (C-124)
The title compound was made following general procedure in Scheme 6, substituting (S)-l-methyl-pyrrolidine-2-carboxylic acid for (S)-2-tert-butoxycarbonylamino- propionic acid. !H ΝMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.25 (m, 3H), 7.96 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, TTT), 4.03 (m, 2H), 3.40 (m, 5H), 2.99 (m, IH ), 2.68 (m, IH), 2.49 (s, 3H), 2.21 (d, 3H), 2.02 (m, IH), 1.71 (m, 2H), 1.55 (m, 2H), 1.20 (m, 2H); LC/MS (M + H)+ m/z 535.
Figure imgf000118_0002
(S)-2-Methyl-N-{4-[l-(pyrrolidine-2-carbonyI)-piperidin-4-ylsulfamoyI]- naphthalen-l-yl}-benzamide (C-125)
The title compound was made following general procedure in Scheme 6, substituting (S)-pyrrolidine-l,2-dicarboxylic acid 1 -tert-butyl ester for (S)-2-tert- butoxycarbonylamino-propionic acid. *H ΝMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.25 (m, 3H), 7.96 (d,.lH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.03 (m, 2H), 3.40 (m, TTT), 3.02 (m, 2H ), 2.78 (m, 2H), 2.49 (s, 3H), 2.06 (m, IH), 1.62 (m, 5H), 1.25 (m, 2H); LC/MS (M + H)+ m/z 521.
Figure imgf000119_0001
(S)-N-{4-[l-(2-Amino-butyryl)-piperidin-4-ylsulfamoyl]-naphthaIen-l-yI}-2- methyl-benzamide (C-126)
The title compound was made following general procedure in Scheme 6, substituting (S)-2-tert-butoxycarbonylamino-butyric acid for (S)-2-tert-butoxycarbonylamino- propionic acid. 1H ΝMR (300 MHz, MeOD) δ 8.71 (d, IH), 8.28 (m, 3H), 7.96 (d, IH), 7.71 (m, 3H), 7.43 (m, IH ), 7.38 (m, 2H), 4.09 (m, IH), 3.78 (m, TTT), 3.01 (m, 2H ), 2.71 (m, IH), 2.49 (s, 3H), 1.57 (m, TTT), 1.25 (m, 4H), 0.82 (m, 3H); LC/MS (M + H)+ m/z 509.
Figure imgf000119_0002
(±)-cis-2-Methyl-N-{4-[3-methyl-l-((s)-pyrro!idine-2-carbonyl)-piperidin-4- ylsulfamoyl]-naphthalen-l-yl}-benzamide (C-127) (mixture of two diastereomers) The title compound (mixture of disatereomers) was made following general procedure in scheme 6, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester, and substituting (s)-pyrrolidine- 1,2-dicarboxylic acid 1 -tert-butyl ester for (s)-2-tert-butoxycarbonylamino-propionic acid. LC/MS (M + H)+ m/z 535.
Figure imgf000119_0003
(±)-(cw)-N-[4-(3-Ethyl-piperidin-4-ylsulfamoyI)-naphthaIen-l-yl]-2-methyl- benzamide (C-128)
The title compound was prepared as its formate salt following general procedure in scheme 4-2, substituting (±)-l-benzyl-3-ethyl-piperidin-4-ylamine (3) for (±)-4- amino- l-benzyl-piperidine-3 -carboxylic acid ethyl ester (6). 'H ΝMR (300 MHz, MeOD) δ 8.84 (d, IH), 8.53 (s, IH), 8.35 (d, IH), 8.26 (d, IH), 7.96 (d, IH), 7.73 (m, 3H), 7.38 (m, 3H), 3.55 (m, IH), 3.05 (m, 3H), 2.92 (m, IH), 2.55 (s, 3H), 1.68 (m, 3H), 1.00 (m, 2H), 0.42 (t, 3H); LC/MS m/z 452 (M + H)+
Figure imgf000120_0001
(±)-(tr «5')-N-[4-(3-Ethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-129)
The title compound was prepared as its formate salt following general procedure in scheme 4-2, substituting (±)-l -benzyl-3 -ethyl-piperidin-4-ylamine (3) for (±)-4- amino-l-benzyl-piperidine-3-carboxylic acid ethyl ester (6). !H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.53 (s, IH), 8.33 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.72 (m, 3H), 7.40 (m, 3H), 3.35 (m, IH), 3.20 (m, 2H), 2.85 (m, IH), 2.60 (m, IH), 2.56 (s, 3H), 1.75 (m, IH), 1.52 (m, 3H), 0.90 (m, IH), 0.58 (t, 3H); LC/MS m/z 452 (M + H)+
Figure imgf000120_0002
(±)-(cw)-(2-{3-Ethyl-4-[4-(2-methyI-benzoylamino)-naphthalene-l- sulfonylamino]-piperidin-l-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester (C- 130) The title compound was made following general procedure in Scheme 6, substituting (±)-(cw)-N-[4-(3-ethyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-2-methyl- benzamide (C-128) for N-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]-benzamide (C-l) and substituting tert-butoxycarbonylamino-acetic acid for 3-tert- butoxycarbonylamino-butyric acid. 1H ΝMR (300 MHz, MeOD) δ 8.85 (d, IH), 8.33 (d, IH), 8.25 (d, IH), 7.95 (d, IH), 7.71 (m, 3H), 7.43 (m, IH), 7.36 (m, 2H), 3.80 (s, 2H), 3.45 (m, 3H), 3.25 (m, TTT), 2.56 (s, 3H), 1.40 (m, 12H), 1.04 (m, TTT), 0.50 (m, 3H); LC/MS m/z 609 (M + H)+
Figure imgf000121_0001
(±)-(cw)-N-{4-[l-(2-Amino-acetyI)-3-ethyI-piperidin-4-ylsulfamoyI]-naphthalen- l-yl}-2-methyl-benzamide (C-131)
The title compound was prepared as its formate salt following general procedure in Scheme 6, substituting (±)-(cw)-N-[4-(3-ethyl-piperidin-4-ylsulfamoyl)-naphthalen- l-yl]-2-methyl-benzamide (C-128) forN-[4-(piperidin-4-ylsulfamoyl)-naphthalen-l- yl]-benzamide (C-l), and substituting tert-butoxycarbonylamino-acetic acid for 3- tert-butoxycarbonylamino-butyric acid. 'HΝMR (300 MHz, MeOD) δ 8.85 (d, IH), 8.52 (s, IH), 8.33 (d, IH), 8.25 (d, IH), 7.95 (d, IH), 7.72 (m, 3H), 7.43 (m, IH), 7.36 (m, 2H), 3.78 (m, 2H), 3.45 (m, 3H), 3.20 (m, 2H), 2.56 (s, 3H), 1.45 (m, 3H), 1.05 (m, 2H), 0.50 (m, 3H); LC/MS m/z 509 (M + H)+
Figure imgf000121_0002
(±)-(trα i5')-N-{4-[l-(2-Amino-acetyl)-3-ethyl-piperidin-4-ylsulfamoyl]- naphthalen-l-yl}-2-methyl-benzamide (C-132) The title compound was prepared as its formate salt following general procedure in Scheme 6, substituting (±)-(trαrø)-N-[4-(3-ethyl-piperidin-4-ylsulfamoyl)- naphthalen-l-yl]-2 -methyl-benzamide (C-129) for N-[4-(piperidin-4-ylsulfamoyl)- naphthalen-l-yl]-benzamide (C-l) and substituting tert-butoxycarbonylamino-acetic acid for 3-tert-butoxycarbonylamino-butyric acid. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.52 (s, IH), 8.33 (d, IH), 8.25 (d, IH), 7.95 (d, IH), 7.72 (m, 3H), 7.43 (m, IH), 7.36 (m, 2H), 4.25 (m, IH), 3.75 (m, 2H), 3.55 (m, IH), 3.05 (m, 2H), 2.56 (s, 3H), 2.50 (m, IH), 1.40 (m, 4H), 0.85 (m, IH), 0.65 (m, 3H); LC MS m/z 509 (M + H)+
Figure imgf000122_0001
(±)-(c s)-N-{4-[3-EthyI-l-(2-ethylamino-acetyl)-piperidin-4-ylsulfamoyl]- naphthalen-l-yl}-2-methyl-benzamide (C-133)
To a 25 °C solution of (±)-(cώ)-N-{4-[l-(2-amino-acetyl)-3-ethyl-piperidin-4- ylsulfamoyl]-naphthalen-l-yl}-2-methyl-benzamide (C-131) (65 mg, 0.128 mmol) in MeOH (4 mL) was added acetyl aldehyde (5.62 mg, 0.128 mmol) and sodium cyanoborohydride (40 mg, 0.64 mmol). After stirring for 2h at 25 °C, the solution was concentrated in vacuo to give a solid. The resultant solid was purified by reverse phase HPLC to provide the title compound. 1H ΝMR (300 MHz, MeOD) δ 8.85 (d, IH), 8.33 (d, IH), 8.25 (d, IH), 7.94 (d, IH), 7.71 (m, 3H), 7.43 (m, IH), 7.35 (m, 2H), 3.55 (m, 5H), 3.20 (m, 2H), 2.85 (m, 2H), 2.56 (s, 3H), 1.25 (m, 7H), 0.50 (m, 3H); LC/MS m/z 537 (M + H)+
Scheme 7
Deprotection in scheme 4
Figure imgf000123_0001
C-28 17
Figure imgf000123_0003
N-{4-[l-(2-bromo-acetyl)-3-cw-methyl-piperidin-4-ylsulfamoyl]-naphthalen-l- yl}-2-methyl-benzamide (17)
(±)-cis-N- [4-( 1 -Benzyl-3 -methyl-piperidin-4-ylsulfamoyl)-naphthalen- 1 -yl] -2- methyl-benzamide (A-21) was prepared as described previously according to the general procedure in Scheme 2. Deprotection of A-21 to afford 2-Methyl-N-[4-(3- c/ -methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yl] -benzamide (C-28) was achieved according to the general procedure described in Scheme 4-2. 2-Methyl-N- [4-(3 -cώ-methyl-piperidin-4-ylsulfamoyl)-naphthalen- 1 -yl] -benzamide (C-28) (700 mg, 1.6 mmol) was dissolved in dichloromethane (8 mL). Triethylamine (192 mg, 0.26 mL, 1.9 mmol) was added followed by bromoacetyl chloride (378 mg, 0.20 mL, 2.4 mmol). The reaction was stirred for 1 hour at room temperature and then passed through a plug of silica gel. Elution with ethyl acetate followed by evaporation in vacuo afforded the title product (644 mg, 72%) as a white solid. This material was used without further purification. LC/MS m/z 556 (M - H)".
Figure imgf000124_0001
(±)-4-(2-{3-c s-methyI-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino]-piperidin-l-yl}-2-oxo-ethyl)-piperazine-l-carboxylic acid tert- butyl ester (C-134) N-{4-[l-(2-Bromo-acetyl)-3-cώ-methyl-piperidin-4-ylsulfamoyl]-naphthalen-l-yl}- 2-methyl-benzamide (100 mg, 0.18 mM) was dissolved in a mixture of acetonitrile (1 mL) and water (0.25 mL). Potassium carbonate (37 mg, 0.27 mmol) was added followed by piperazine-1 -carboxylic acid tert-butyl ester (37 mg, 0.2 mM). The reaction was stirred for 1 hour at room temperature before being passed through a plug of silica gel. Elution with ethyl acetate :methanol (90: 10) afforded the titled compound (43 mg, 34%) as a yellow solid. 1H ΝMR (300 MHz, CD3OD) (1:1 mixture of rotamers) δ 8.85 (d, IH), 8.30 (d, IH), 8.22 (d, IH), 7.95 (d, IH), 7.70 (m, 3H), 7.38 (m, 4H), 3.57 (m, 5H), 3.40 (m, 6H), 3.18 (m, 4H), 2.58 (s, 3H), 1.78 (m, IH), 1.52 (m, 2H), 1.42 (s, 9H), 0.70 (d, 1.5H), 0.65 (d, 1.5H); LC/MS m/z 66A (M + H)+.
Figure imgf000124_0002
(±)-2-methyl-N-{4-[3-cw-methyl-l-(2-piperazin-l-yl-acetyl)-piperidin-4- ylsulfamoyl]-naphthalen-l-yl}-benzamide (C-135) (±)-4-(2-{3-cώ-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l- sulfonylamino] -piperidin- 1 -yl } -2-oxo-ethyl)-piperazine- 1 -carboxylic acid tert-butyl ester (43 mg, 0.07 mmol) was dissolved in a solution of 4N HCl/dioxane (3 mL). The reaction was left standing for 3 hours at room temperature; concentration in vacuo afforded the titled compound (14 mg, 40%) as its bis-hydrochloride salt. !H NMR (300 MHz, CD3OD) (1:1 mixture of rotamers) δ 8.85 (d, IH), 8.32 (d, IH), 8.24 (d, IH), 7.96 (d, IH), 7.72 (m, 3H), 7.40 (m, 4H), 4.30 (m, 2H), 3.52 (m, 12H), 3.22 (m, 2H), 2.58 (s, 3H), 1.83 (m, IH), 1.58 (m, 2H), 0.74 (d, 1.5H), 0.68 (d, 1.5H); LC/MS m/z 564 (M + H)+.
Figure imgf000125_0001
(±)-cra-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthaIene-l-suIfonylamino]- piperidine-1-carboxylic acid ethyl ester (C-136)
The title compound was prepared from A-21 according to the general procedure in Scheme 7. To a solution of A-21 in ethyl acetate was added Pd(OH)2 and diethyl pyrocarbonate (1.0 eq). The vessel was evacuated and pressurized to 50 psi H and allowed to agitate on a Parr apparatus overnight. The solution was filtered through a celite plug, washed with hot ethyl acetate and concentrated at 40°C at reduced pressure. The residue was purified using flash chromatography to provide the title compound. 1H NMR (300 MHz, DMSO) δ 10.63 (s, TTT), 8.77 (d, IH), 8.28 (d, IH), 8.21 (d, IH), 8.12 (d, IH), 7.97 (d, IH), 7.74 (m, 3H), 7.45 (d, IH), 7.38 (m, 2H), 3.98 (q, 2H), 3.38(m, IH), 3.29 (m, IH), 3.21 (m, 3H), 2.52 (s, 3H), 1.67 (m,lH), 1.30 (m, 2H), 1.13 (t, 3H), 0.57 (d, 3H); LC/MS m/z 508 (M - HT, 510 (M + H)+
Figure imgf000125_0002
cw-3-Methyl-4-[4-(2-methyl-benzoylamino)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid ethyl ester (single enantiomer, absolute stereochemistry not determined) (C-137)
Compound C-136 was subjected to reverse phase chiral HPLC separation, and the title compound was the first enantiomer to elute from the column. !H NMR (300 MHz, DMSO) δ 8.70 (d, IH), 8.42 (d, IH), 8.34 (d, IH), 8.11 (s, IH), 7.93 (d, IH), 7.63 (m, 3H), 7.42 (d, IH), 7.34 (d, 2H), 4.64 (d, IH), 4.05 (m, 2H), 3.48 (m, 0.5H), 3.38 (m, IH), 3.21 (m, 2.5H), 2.59 (s, 3H), 1.74 (m, IH), 1.48 (s, IH), 1.43 (m, 2H), 1.19 (t, 3H), 0.66 (s, 3H. LC/MS m/z 508 (M - H)\ 510 (M + H)+
Figure imgf000126_0001
cis-3-Methyl-4-[4-(2-methyl-benzoyIamino)-naphthaIene-l-sulfonyIamino]- piperidine-1-carboxylic acid ethyl ester (single enantiomer, absolute stereochemistry not determined) (C-138) Compound C-136 was subjected to reverse phase chiral HPLC separation, and the title compound was the second enantiomer to elute from the column. !H NMR (300 MHz, DMSO) δ 8.70 (d, IH), 8.42 (d, IH), 8.34 (d, IH), 8.11 (s, IH), 7.93 (d, IH), 7.63 (m, 3H), 7.42 (d, IH), 7.34 (d, 2H), 4.64 (d, IH), 4.05 (m, 2H), 3.48 (m, 0.5H), 3.38 (m, IH), 3.21 (m, 2.5H), 2.59 (s, 3H), 1.74 (m, IH), 1.48 (s, IH), 1.43(m, 2H), 1.19 (t, 3H), 0.66 (s, 3H). LC/MS m/z 508 (M - H)\ 510 (M + H)+
Figure imgf000126_0002
(±)-cw-N-[4-(l-Butyryl-3-methyl-piperidin-4-yIsulfamoyl)-naphthalen-l-yl]-2- methyl-benzamide (C-139) The title compound was prepared from A-21 according to the general procedure in Scheme 7. To a solution of A-21 in ethyl acetate was added Pd(OH)2 and butyric anhydride (1.0 eq). The vessel was evacuated and pressurized to 50 psi H2 and allowed to agitate on a Parr apparatus overnight. The solution was filtered through a celite plug, washed with hot ethyl acetate and concentrated at 40°C at reduced pressure. The residue was purified using flash chromatography to provide the title compound. 'H NMR (300 MHz, DMSO) δ (m, IH), 8.32 (m, 3H), 7.95 (d, IH), 7.63 (m, 3H), 7.43 (m, IH), 7.33 (m, 2H), 5.20 (d, IH), 3.63 (m, 0.5H), 3.40 (m, 2H), 3.20 (m, 2H), 3.01 (m, 0.5H), 2.57 (s, 3H), 2.19 (m, TTT), 1.82 (m, 0.5H), 1.67 (m, 0.5H), 1.56 (m, 3H), 1.30 (m IH), 0.95 (dt, 3H), 0.73 (d, 0.5H), 0.59 (d, 0.5H). LC/MS m/z 506 (M - H)", 508 (M + H)+.
Figure imgf000127_0001
cώ-N-[4-(l-butyryI-3-methyl-piperidin-4-ylsulfamoyl)-naphthalen-l-yI]-2- methyl-benzamide (C-140) (single enantiomer, absolute stereochemistry not determined) Compound C-139 was subjected to reverse phase chiral HPLC separation, and the title compound was the first enantiomer to elute from the column. !H ΝMR (300 MHz, CDC13) δ 8.71 (m, IH), 8.42 (d, IH), 8.37 (d, IH), 8.12 (s, IH), 7.94 (d, IH), 7.73 (m, IH), 7.63 (m, 2H), 7.43 (m, IH), 7.34 (d, 2H), 4.68 (m, IH), 3.42-3.20 (m, 3H), 2.59 (s, 3H), 2.20 (m, 2H), 1.57 (m, 4H), 1.35 (m, IH), 1.25 (m, 2H), 0.89 (m, 3H), 0.74 (d, 1.5H), 0.55 (d, 1.5H). LC/MS m/z 506 (M - H)_, 508 (M + H)+.
Figure imgf000127_0002
-N-[4-(l-butyryl-3-methyl-piperidin-4-ylsuIfamoyI)-naphthalen-l-yl]-2- methyl-benzamide (C-141) (single enantiomer, absolute stereochemistry not determined) , Compound C-139 was subjected to reverse phase chiral HPLC separation, and the title compound was the second enantiomer to elute from the column. !H NMR (300 MHz, CDC13) δ 8.71 (m, IH), 8.42 (d, IH), 8.37 (d, IH), 8.12 (s, IH), 7.94 (d, IH), 7.73 (m, IH), 7.63 (m, 2H), 7.43 (m, IH), 7.34 (d, TTT), 4.68 (m, IH), 3.42-3.20 (m, 3H), 2.59 (s, 3H), 2.20 (m, 2H), 1.57 (m, 4H), 1.35 (m, IH), 1.25 (m, 2H), 0.89 (m, 3H), 0.74 (d, 1.5H), 0.55 (d, 1.5H). LC/MS m/z 506 (M - HV, 508 (M + H)+.
Figure imgf000128_0001
(±)-2-Methyl-N-{4-[cw-3-methyl-l-(2-pyrrolidin-l-yl-acetyl)-piperidin-4- ylsulfamoyl]-naphthalen-l-yl}-benzamide (C-142)
The title compound was prepared as shown in Scheme 7 for the preparation of C- 134 except substituting pyrrolidine for piperazine-1 -carboxylic acid tert-butyl ester. Reverse phase HPLC purification afforded the title compound as its formate salt. Wt.: 37 mg (38%). !H ΝMR (300 MHz, CD3OD) (1 : 1 mixture of rotamers) δ 8.85 (d, IH), 8.47 (s, IH), 8.36 (d, IH), 8.27 (d, IH), 7.96 (d, IH), 7.70 (m, 3H), 7.40 (m, 3H), 4.22 (m, 2H), 3.68 (m, IH), 3.45 (m, 4H), 3.24 (m, 4H), 2.58 (s, 3H), 2.04 (m, 4H), 1.80 (m, IH), 1.47 (m, 2H), 0.70 (d, 1.5H), 0.65 (d, 1.5H); LC/MS m/z 549 (M + H)+.
Figure imgf000128_0002
(±)-2-Methyl-N-{4-[c/-f-3-methyl-l-(2-piperidin-l-yl-acetyl)-piperidin-4- ylsulfamoyI]-naphthalen-l-yl}-benzamide (C-143)
The title compound was prepared as shown in Scheme 7 for the preparation of C- 134 except substituting piperidine for piperazine-1 -carboxylic acid tert-butyl ester. Reverse phase HPLC purification afforded the title compound as its formate salt. Wt.: 43 mg (43 %). *HΝMR (300 MHz, CD3OD) (1:1 mixture of rotamers) δ 8.85 (d, IH), 8.33 (d, 2H), 8.25 (d, IH), 7.95 (d, IH), 7.70 (m, 3H), 7.40 (m, 3H), 4.04 (m, 2H), 3.63 (m, IH), 3.45 (m, 4H), 3.20 (m, 4H), 2.56 (s, 3H), 1.88 (m, 6H), 1.67 (m, 2H), 1.45 (m, IH), 0.70 (d, 1.5H), 0.64 (d, 1.5H); LC/MS m/z 563 (M + H)+.
Figure imgf000129_0001
(±)-iV-{4-[l-(2-diethylamino-acetyl)-3-cw-methyl-piperidin-4-ylsuIfamoyl]- naphthalen-l-yl}-2-methyl-benzamide (C-144)
The title compound was prepared as shown in Scheme 7 for the preparation of C- 134 except substituting diethylamine for piperazine-1 -carboxylic acid tert-butyl ester. Reverse phase HPLC purification afforded the title compound as its formate salt. Wt.: 49 mg (50%). 1H NMR (300 MHz, CD3OD) (1:1 mixture of rotamers) δ 8.85 (d, IH), 8.46 (s, IH), 8.38 (d, IH), 8.28 (d, IH), 7.95 (d, IH), 7.70 (m, 3H), 7.40 (m, 3H), 4.16 (m, 2H), 3.65 (m, IH), 3.44 (m, 4H), 3.19 (m, 4H), 2.56 (s, 3H), 1.80 (m, IH), 1.52 (m, 2H), 1.25 (t, 6H), 0.70 (d, 1.5H), 0.64 (d, 1.5H); LC/MS m/z 551 (M + H)+.
Figure imgf000130_0001
(±)-2-MethyI-N-{4-[3-cω-methyl-l-(2-morpholin-4-yl-acetyl)-piperidin-4- ylsulfamoyl]-naphthalen-l-yl}-benzamide (C-145)
The title compound was prepared as shown in Scheme 7 for the preparation of C- 134 except substituting morpholine for piperazine-1 -carboxylic acid tert-butyl ester. Wt: 60 mg (58%). 1H ΝMR (300 MHz, CD3OD) (1:1 mixture of rotamers) δ 8.88 (d, IH), 8.38 (d, IH), 8.32 (d, IH), 8.00 (d, IH), 7.80 (m, 3H), 7.45 (m, 3H), 4.26 (m, 2H), 4.06 (m, 2H), 3.86 (m, 3H), 3.50 (m, 4H), 3.24 (m, 3H), 2.60 (s, 3H), 1.85 (m, IH), 1.55 (m, 2H), 0.76 (d, 1.5H), 0.69 (d, 1.5H); LC MS m/z 565 (M + H)+.
Figure imgf000130_0002
N-{4-[l-(2-Diethylamino-acetyl)-piperidin-4-ylsulfamoyl]-naphthaIen-l-yI}-2- methyl-benza ide (C-146)
The title compound was prepared following the general procedure for preparing C- 134 in Scheme 7, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for 1 -benzyl-3 -methyl-piperidin-4-ylamine, and diethyl amine for piperazine-1 - carboxylic acid tert-butyl ester. 'H ΝMR (300 MHz, DMSO) δ 10.66 (s, IH), 9.08 (m, IH), 8.69 (d, IH), 8.27 (d, IH), 8.22 (t, 2H), 7.94 (d, IH), 7.70 (m, 3H), 7.42 (m, IH), 7.35 (m, 2H), 4.27-4.02 (m, 2H), 4.03 (d, IH), 3.40 (m, 3H), 2.98 (m, 3H), 2.83 (m, IH), 2.56 (s, 3H), 1.92 (m,5 TT), 1.58 (m, 2H), 1.30 (m, 2H), 1.11 (t, 2H). LC/MS m/z 536 (M - TT) , 538 (M + H)+
Figure imgf000131_0001
2-Methyl-N-{4-[l-(2-pyrrolidin-l-yl-acetyl)-piperidin-4-yIsulfamoyl]- naphthalen-l-yl}-benzamide (C-147)
The title compound was prepared following the general procedure for preparing C- 134 in Scheme 1, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for 1 -benzyl-3 -methyl-piperidin-4-ylamine, and pyrrole for piperazine-1 -carboxylic acid tert-butyl ester. !H ΝMR (300 MHz, DMSO) δ 10.56 (s, IH), 9.28 (m, IH), 8.68 (d, IH), 8.27 (d, IH), 8.21 (m, 2H), 7.94 (d, IH), 7.72 (m, 3H), 7.43 (d, IH), 7.38 (m, 2H), 4.31 (m, 2H), 4.03 (d, IH), 3.27 (m, 2H), 2.98 (m, 3H), 2.83 (m, IH), 2.56 (s, 3H), 1.92 (m, 5H), 1.58 (m, 2H), 1.3 (m, TTT). LC/MS m/z 534 (M - H)\ 535 (M + H)+
Figure imgf000131_0002
2-Methyl-N-{4-[l-(2-piperidin-l-yl-acetyl)-piperidin-4-ylsulfamoyl]- naphthalen-l-yl}-benzamide (C-148)
The title compound was prepared following the general procedure for preparing C- 134 in Scheme 7, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for 1 -benzyl-3 -methyl-piperidin-4-ylamine, and substituting piperidine for piperazine-1 -carboxylic acid tert-butyl ester. 'H ΝMR (300 MHz, DMSO) δ 10.56 (s, IH), 9.28 (m, IH), 8.68 (d, IH), 8.27 (d, IH), 8.21 (m, 2H), 7.94 (d, IH), 7.72 (m, 3H), 7.43 (d, IH), 7.38 (m, TTT), 4.15 (m, 3H), 3.36 (m, 3H), 2.99 (m, IH), 2.80 (m, 3H), 2.56 (s, 3H), 1.74 (m, 3H), 1.58 (m, 4H), 1.27 (m, 3H). LC/MS m/z 548 (M - H)", 549 (M + H)+
Scheme 8
Figure imgf000132_0001
Figure imgf000132_0002
(±)-(c/s)-4-Amino-naphthalene-l-sulfonic acid (l-butyryI-3-methyI-piperidin-4- yl)-amide (D-l)
(±)-cώ-N- [4-( 1 -B enzyl-3 -methyl-piperidin-4-ylsulfamoyl)-naphthalen- 1 -yl] -2- methyl-benzamide (18) was prepared as described previously according to the general procedure in Scheme 3, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for />-anisidine. (±)-(ci$)-A-( 1 ,3-Dioxo- 1 ,3-dihydro-isoindol-2-yl)-naphthalene- 1 - sulfonic acid (3-methyl-piperidin-4-yl)-amide (C-74) and (±)-(cώ)-4-(l,3-dioxo-l,3- dihydro-isoindol-2-yl)-naphthalene-l-sulfonic acid (l-butyryl-3-methyl-piperidin-4- yl)-amide (C-75) were prepared as described previously according to the general procedure in Scheme 5. The title compound was made following general procedure in Scheme 3, substituting (±)-(cώ)-4-(l,3-dioxo-l,3-dihydro-isoindol-2-yl)- naphthalene-1 -sulfonic acid (l-butyryl-3-methyl-piperidin-4-yl)-amide (C-75) for 4- (1,3 -dioxo- 1 ,3 -dihydro-isoindol-2-yl) -naphthalene- 1 -sulfonic acid (4-methoxy- phenyl)-amide (A-2). *H ΝMR (300 MHz, MeOD) δ 8.62 (d, IH), 8.30 (d, IH), 7.98 (d, IH), 7.60 (dt, IH), 7.48 (dt, IH), 6.70 (d, IH), 3.66 (m, IH), 3.42 (m, IH), 3.28 (m, 5H), 2.25 (m, 2H), 1.67 (m, IH), 1.50 (m, TTT), 1.30 (m, 2H), 0.88 (t, 3H), 0.64 (m, 3H); LC/MS m/z 391 (M + H)+
Figure imgf000133_0001
(±)-(c 5)-4-(4-Amino-naphthaIene-l-sulfonylamino)-3-methyI-piperidine-l- carboxylic acid ethyl ester (D-2)
The title compound was made following general procedure in Scheme 8, substituting ethyl chloroformate for butyryl chloride. *H NMR (300 MHz, MeOD) δ 8.61 (d, IH), 8.10 (d, IH), 7.97 (d, IH), 7.60 (t, IH), 7.48 (t, IH), 6.70 (d, IH), 4.02 (q, 2H), 3.47 (m, IH), 3.24 (m, 4H), 1.64 (m, IH), 1.38 (m, IH), 1.25 (m, IH), 1.17 (t, 3H), 0.64 (d, 3H); LC/MS m/z 393 (M + H)+
Figure imgf000133_0002
(±)-(cw)-N-[4-(l-Butyryl-3-methyl-piperidin-4-y!sulfamoyl)-naphthalen-l-yl]-2- methyl-nicotinamide (D-3)
To a solution of naphthalenyl amine (D-l) (78 mg, 0.2 mmol) in CH2C1 (3 mL) was added acetyl chloride (20 uL, 0.24 mmol) and Et3Ν (60 uL, 0.4 mmol). The resultant solution was stirred at 25 °C overnight. The solvent was removed in vacuo and the residue was purified using HPLC to give the title compound. !H NMR (300 MHz, MeOD) δ 8.84 (d, IH), 8.57 (dd, TTT), 8.31 (d, IH), 8.24 (d, IH), 8.11 (m, IH), 7.98 (m, IH), 7.72 (m, 2H), 7.43 (dd, IH), 3.40 (m, 5H), 2.75 (s, 3H), 2.25 (m, 2H), 1.50 (m, 5H), 0.90 (t, 3H), 0.65 (dd, 3H); LC/MS m/z 510 (M + H)+
Figure imgf000133_0003
(±)-(c«)-3-Methyl-pyridine-2-carboxylic acid [4-(l-butyryl-3-methyl-piperidin- 4-ylsuIfamoyI)-naphthaIen-l-yl]-amide (D-4) The title compound was made following general procedure in Scheme 8, substituting 3-methyl-pyridine-2-carbonyl chloride for 2-methyl-nicotinoyl chloride. JH NMR (300 MHz, MeOD) δ 8.83 (m, IH), 8.59 (d, IH), 8.28 (m, 3H), 7.74 (m, 3H), 7.53 (dd, IH), 3.40 (m, 5H), 2.75 (s, 3H), 2.25 (m, 2H), 1.50 (m, 5H), 0.95 (t, 3H), 0.80 (dd, 3H); LC/MS m/z 510 (M + H)+
Figure imgf000134_0001
(±)-(c-s)-3,5-DimethyI-isoxazole-4-carboxylic acid [4-(l-butyryl-3-methyl- piperidin-4-ylsuIfamoyl)-naphthalen-l-yl]-amide (D-5) The title compound was made following general procedure in Scheme 8, substituting 3,5-dimethyl-isoxazole-4-carbonyl chloride for 2-methyl-nicotinoyl chloride. *H NMR (300 MHz, MeOD) δ 8.82 (d, IH), 8.28 (d, IH), 8.18 (d, IH), 7.93 (d, IH), 7.71 (m, TTT), 3.34 (m, 5H), 2.70 (s, 3H), 2.47 (s, 3H), 2.25 (m, 2H), 1.50 (m, 5H), 0.89 (t, 3H), 0.63 (dd, 3H); LC/MS m/z 514 (M + H)+
Figure imgf000134_0002
(±)-(cw)-3-MethyI-4-{4-[(2-methyl-pyridine-3-carbonyl)-amino]-naphthalene-l- sulfonylamino}-piperidine-l-carboxylic acid ethyl ester (D-6)
The title compound was made following general procedure in Scheme 8, substituting (±)-(cω)-4-(4-amino-naphthalene- 1 -sulfonylamino)-3 -methyl-piperidine- 1 - carboxylic acid ethyl ester (D-2) for (±)-(cώ)-4-amino-naphthalene-l -sulfonic acid (l-butyryl-3-methyl-piperidin-4-yl)-amide (D-l). 1H NMR (300 MHz, MeOD) δ 8.83 (d, IH), 8.56 (dd, IH), 8.31 (d, IH), 8.23 (d, IH), 8.12 (d, IH), 7.97 (d, 1H),7.71 (m, 2H), 7.43 (dd, IH), 4.03 (q, 2H), 3.48 (m, IH), 3.28 (m, 4H), 2.75 (s, 3H), 1.68 (m, IH), 1.40 (m, IH), 1.29 (m, IH), 1.18 (t, 3H), 0.64 (d, 3H); LC/MS m/-. 512 (M + H)+
Figure imgf000135_0001
(±)-(cw)-3-Methyl-4-{4-[(3-methyl-pyridine-2-carbonyl)-amino]-naphthalene-l- sulfonyIamino}-piperidine-l-carboxylic acid ethyl ester (D-7) The title compound was made following general procedure in Scheme 8, substituting (±)-(cώ)-4-(4-amino-naphthalene- 1 -sulfonylamino)-3 -methyl-piperidine- 1 - carboxylic acid ethyl ester (D-2) for (±)-(cώ)-4-amino-naphthalene-l -sulfonic acid (l-butyryl-3-methyl-piperidin-4-yl)-amide (D-l), and substituting 3-methyl- pyridine-2-carbonyl chloride for 2-methyl-nicotinoyl chloride. !H NMR (300 MHz, MeOD) δ 8.82 (m, IH), 8.56 (d, IH), 8.28 (m, IH), 8.18 (m, IH), 7.74 (m, 3H), 7.59 (dd, IH), 4.02 (q, 2H), 3.48 (m, IH), 3.28 (m, 4H), 2.73 (s, 3H), 1.68 (m, IH), 1.40 (m, IH), 1.28 (m, IH), 1.17 (t, 3H), 0.63 (d, 3H); LC/MS m/z 512 (M + H)+
Figure imgf000135_0002
(±)-(c s)-4-{4-[(3,5-DimethyI-isoxazole-4-carbonyl)-amino]-naphthalene-l- sulfonylammo}-3-methyl-piperidine-l-carboxylic acid ethyl ester (D-8)
The title compound was made following general procedure in Scheme 8, substituting (±)-(cώ)-4-(4-amino-naphthalene- 1 -sulfonylamino)-3-methyl-piperidine- 1 - carboxylic acid ethyl ester (D-2) for (±)-(cώ)-4-amino~naphthalene-l -sulfonic acid (l-butyryl-3-methyl-piperidin-4-yl)-amide (D-l) and substituting 3,5-dimethyl- isoxazole-4-carbonyl chloride for 2-methyl-nicotinoyl chloride. 1H NMR (300 MHz, MeOD) δ 8.82 (d, IH), 8.27 (d, IH), 8.18 (d, IH), 7.93 (d, IH), 7.71 (m, TTT), 4.03 (q, TTT), 3.30 (m, 5H), 2.70 (s, 3H), 2.47 (s, 3H), 1.68 (m, IH), 1.40 (m, IH), 1.28 (m, IH), 1.18 (t, 3H), 0.64 (d, 3H); LC/MS m/z 516 (M + H)+
Figure imgf000136_0001
(±)-(trα«5')-3-Methyl-4-{4-[(2-methyl-pyridine-3-carbonyl)-amino]-naphthalene- l-sulfonylamino}-piperidine-l-carboxylic acid ethyl ester (D-9)
The title compound was made following general procedure in Scheme 8, substituting (±)-(trarø)-4-(4-amino-naphthalene- 1 -sulfonylamino)-3 -methyl-piperidine- 1 - carboxylic acid ethyl ester for (±)-(cώ)-4-amino-naphthalene-l -sulfonic acid (1- butyryl-3-methyl-piperidin-4-yl)-amide (D-l). !H NMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.58 (dd, IH), 8.32 (d, IH), 8.23 (d, IH), 8.12 (d, IH), 7.98 (d, IH), 7.72 (m, 2H), 7.44 (dd, IH), 4.04 (q, 2H), 3.88 (m, 2H), 3.28 (m, IH), 2.82 (m, IH), 2.75 (s, 3H), 2.65 (m, IH), 2.38 (s, br, IH), 1.40 (m, 2H), 1.18 (t, 3H), 0.57 (d, 3H); LC/MS m/z 512 (M + H)+
Figure imgf000136_0002
(±)-(tr «5,)-N-[4-(l-Butyryl-3-methyl-piperidin-4-yIsulfamoyl)-naphthaIen-l-yl]- 2-methyl-nicotinamide (D-10)
The title compound was made following general procedure in Scheme 8, substituting (±)-(trα.ω)-4-amino-naphthalene- 1 -sulfonic acid ( 1 -butyryl-3 -methyl-piperidin-4- yl)-amide for (±)-(cώ)-4-amino-naphthalene-l -sulfonic acid (1 -butyryl-3 -methyl- piperidin-4-yl)-amide (D-l). 'H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.57 (dd, IH), 8.31 (d, IH), 8.23 (d, IH), 8.12 (d, IH), 7.98 (d, IH), 7.72 (m, 2H), 7.42 (dd, IH), 4.28 (t, IH), 3.72 (m, IH), 2.90 (m, IH), 2.74 (s, 3H), 2.56 (m, IH), 2.23 (m, 3H), 1.53 (m, 3H), 1.28 (m, 2H), 0.89 (m, 3H), 0.61 (dd, 3H); LC/MS m/z 510 (M + H)+
Scheme 9
Figure imgf000137_0001
Figure imgf000137_0002
Cyclopentanecarboxylic acid [4-(piperidin-4-yIsuIfamoyI)-naphthalen-l-yl]- amide (D-11)
4-[4-(l,3-Dioxo-l,3-dihydro-isoindol-2-yl)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester (19) was prepared according to the general procedure in Scheme 3, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for / -anisidine.
4-(4-Amino-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester (20) was prepared according to the general procedure in Scheme 3 substituting 4-[4-( 1 ,3 -dioxo- 1 ,3 -dihydro-isoindol-2-yl)-naphthalene- 1 -sulfonylamino] - piperidine- 1 -carboxylic acid tert-butyl ester for 4-(l,3-dioxo-l,3-dihydro-isoindol-2- yl)-naphthalene-l -sulfonic acid (4-methoxyphenyl)-amide.
4-[4-(Cyclopentanecarbonyl-amino)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (21) was prepared according to the general procedure in Scheme 3, substituting cyclopentanecarbonyl chloride for acetyl chloride.
The title compound (D-11) was prepared according to Scheme 9 by following the general deprotection strategy in Scheme 4-1. *H NMR (300 MHz, DMSO) δ 10.15 (s, IH), 8.66 (m, IH), 8.58 (m, IH), 8.41 (m, IH), 8.26 (m, 2H), 8.12 (d, IH), 7.94 (d, IH), 7.71 (m, TTT), 3.11 (m, 3H), 2.82 (m, 2H), 1.94 (m, 2H), 1.86-1.40 (m, 10H). LC/MS m/z 400 (M - TT)', 402 (M + H)+
Figure imgf000138_0001
Cyclopropanecarboxylic acid [4-(piperidin-4-ylsulfamoyl)-naphthalen-l-yl]- amide (D-12)
The title compound was made following the general procedure in Scheme 9, substituting cyclopropanecarbonyl chloride for cyclopentanecarbonyl chloride. !H NMR (300 MHz, DMSO) δ 10.49 (s, IH), 8.67 (m, IH), 8.54 (m, IH), 8.39 (m, IH), 8.26 (d, IH), 8.11 (d, IH), 8.01 (d, IH), 7.73 (m, 2H), 3.56 (s, IH), 3.05 (m, 2H), 2.79 (m, 2H), 2.19 (m, IH), 1.60 (m, 2H), 1.50 (m, 2H), 0.87 (d, 4H). LC/MS m/z 372 (M - H)\ 374 (M + H)+
Figure imgf000138_0002
Cyclobutanecarboxylic acid [4-(piperidin-4-ylsulfamoyI)-naphthalen-l-yI]- amide (D-13)
The title compound was made following the general procedure in Scheme 9, substituting cyclobutanecarbonyl chloride for cyclopentanecarbonyl chloride. 1H NMR (300 MHz, DMSO) δ 9.98 (s, IH), 8.62 (d, IH), 8.21 (d, IH), 8.12 (d, IH), 7.99 (d, IH), 7.95 (d, IH), 7.70 (m, TTT), 3.59 (d, 2H), 3.51 (t, IH), 3.13 (m, IH), 2.67 (m, 2H), 2.32-2.16 (m, 4H), 1.99 (m, IH), 1.84 (m, IH), 1.37 (d, 2H), 1.10 (m, 2H). LC/MS m/z 386 (M - TT)', 388 (M + H)+
Figure imgf000139_0001
Cyclohexanecarboxylic acid [4-(piperidin-4-yIsuIfamoyl)-naphthalen-l-yl]- amide (D-14)
The title compound was made following the general procedure in Scheme 9, substituting cyclohexanecarbonyl chloride for cyclopentanecarbonyl chloride. *H NMR (300 MHz, DMSO) δ 10.07 (s, IH), 8.64 (dd, IH), 8.25 (m,4 TT), 8.12 (d, IH), 7.96 (d, IH), 7.72 (m, 2H), 3.06 (m, 2H), 2.81 (m, 2H), 2.66 (m, 2H), 1.91 (d, 2H), 1.78 (d, 2H), 1.61 (m, 3H), 1.49 (m, 4H), 1.31 (m, 2H). LC/MS m/z 415 (M - H)\ 417 (M + H)+
Figure imgf000139_0002
Cyclopropanecarboxylic acid [4-(l-butyryl-piperidin-4-ylsulfarnoyl)- naphthalen-l-yl]-amide (D-15)
The title compound was made following the general procedure in Scheme 9, substituting cyclopropanecarbonyl chloride for cyclopentanecarbonyl chloride. lTT NMR (300 MHz, DMSO) δ 10.43 (s, IH), 8.64 (m, IH), 8.33 (m, IH), 8.13 (m, IH), 8.02 (d, IH), 7.97 (m, 2H), 3.98 (d, IH), 3.59 (m, IH), 3.19 (m, IH), 2.90 (t, IH), 2.61 (m, IH), 2.13 (m, 3H), 1.40 (m, 4H), 1.16 (m, 2H), 0.84 (d, 4H), 0.80 (t, 3H). LC/MS m/z 442 (M - H)', 444 (M + H)+
Figure imgf000139_0003
Cyclohexanecarboxylic acid [4-(l-butyryl-piperidin-4-ylsulfamoyl)-naphthalen- l-yl]-amide (D-16) The title compound was made following the general procedure in Scheme 9, substituting cyclohexanecarbonyl chloride for cyclopentanecarbonyl chloride. 1H NMR (300 MHz, DMSO) δ 10.05 (s, IH), 8.64 (dd, IH), 8.25 (dd, IH), 8.13 (d, IH), 8.03 (d, IH), 7.91 (d, IH), 7.71 (m, TTT), 3.98 (d, IH), 3.59 (d, IH), 3.18 (m, IH), 2.91 (t, IH), 2.61 (t, IH), 2.16 (t, 2H), 1.90 (d, TTT), 1.77 (m, TTT), 1.67 (m, 2H), 1.49-1.20 (m, 9H), 0.81 (t, 3H). LC/MS m/z 529 (M - H)\ 531 (M + H)+
Figure imgf000140_0001
l-Methyl-piperidine-4-carboxylic acid [4-(piperidin-4-ylsuIfamoyl)-naphthaIen- l-yl]-amide (D-17)
The title compound was made following general procedure in Scheme 9, substituting l-methyl-piperidine-4-carbonyl chloride (prepared in situ from the corresponding acid using oxalyl chloride) for cyclopentanecarbonyl chloride. *H NMR (300 MHz, DMSO) δ 10.39 (s, IH), 8.64 (dd, IH), 8.29 (dd, IH), 8.14 (d, TTT), 8.05 (d, IH), 7.89 (d, IH), 7.72 (m, 2H), 3.62 (d, TTT), 3.40 (m, 2H), 3.15 (m, IH), 2.95 (m, 2H), 2.78-2.67 (m, 6H), 2.09 (m, 2H), 2.00 (m, 2H), 1.84 (m, IH), 1.39 (m, IH), 1.18 (m, 2H). LC/MS m/z 384 (M - H)", 386 (M + H)+
Figure imgf000140_0002
Cyclopentanecarboxylic acid [4-(l-butyryl-piperidin-4-yIsulfamoyl)- naphthalen-l-yl]-amide (D-18)
The title compound was made following the general procedure in Scheme 9. *H NMR (300 MHz, DMSO) δ 10.12 (s, IH), 8.66 (m, IH), 8.28 (m, IH), 8.13 (d, IH), 7.95 (d, IH), 7.71 (m, 2H), 3.98 (d, TTT), 3.59 (d, IH), 3.19 (m, IH), 3.09 (m, IH), 2.90 (m, IH), 2.57 (m, IH), 2.16 (t, 2H), 1.94 (m, 2H), 1.81 (m, 2H), 1.71 (m, 2H), 1.62 (m, 2H), 1.42 (m, 4H), 1.16 (m, 2H), 0.81 (t, 3H). LC/MS m/z 471 (M - H)\ 473 (M + H)+
Figure imgf000141_0001
Cyclobutanecarboxylic acid [4-(l-butyryl-piperidin-4-ylsulfamoyl)-naphthalen- l-yl]-amide (D-19) The title compound was made following the general procedure in Scheme 9, substituting cyclobutanecarbonyl chloride for cyclopentanecarbonyl chloride. *H NMR (300 MHz, DMSO) δ 9.98 (s, IH), 8.62 (d, IH), 8.21 (d, IH), 8.12 (d, IH), 7.99 (d, IH), 7.95 (d, IH), 7.70 (m, 2H), 3.59 (d, 2H), 3.51 (t, IH), 3.13 (m, IH), 2.67 (m, 2H), 2.32-2.16 (m, 4H), 2.16 (t, 2H), 1.99 (m, IH), 1.84 (m, IH), 1.42 (m, 2H), 1.37 (d, 2H), 1.10 (m, 2H), 0.81 (t, 3H). LC/MS m/z 457 (M - H)\ 459 (M + H)+
Figure imgf000141_0002
Tetrahydro-pyran-4-carboxylic acid [4-(l-butyryl-piperidin-4-yIsulfamoyI)- naphthalen-l-yl]-amide (D-20)
The title compound was made following the general procedure in Scheme 9, substituting tetrahydro-pyran-4-carbonyl chloride (prepared in situ from the corresponding acid using oxalyl chloride) for cyclopentanecarbonyl chloride. LC/MS m/z 488 (M + H)+
Figure imgf000141_0003
l-MethyI-piperidine-3-carboxylic acid [4-(piperidin-4-ylsulfamoyl)-naphthaIen- l-yl]-amide (D-22) The title compound was made following the general procedure in Scheme 9, substituting l-methyl-piperidine-3 -carbonyl chloride (prepared in situ from the corresponding acid using oxalyl chloride) for cyclopentanecarbonyl chloride. LC/MS m/z 431 (M + H)+.
Figure imgf000142_0001
l-Methyl-piperidine-3-carboxylic acid [4-(l-butyryl-piperidin-4-ylsulfamoyl)- naphthalen-l-yl]-amide (D-23)
The title compound was made following the general procedure in Scheme 9, substituting l-methyl-piperidine-3 -carbonyl chloride (prepared in situ from the corresponding acid using oxalyl chloride) for cyclopentanecarbonyl chloride. LC/MS m/z 501 (M + H)+.
Figure imgf000142_0002
l-Methyl-piperidine-4-carboxylic acid [4-(l-butyryI-piperidin-4-yIsulfamoyl)- naphthalen-l-yl]-amide (D-24)
The title compound was made following the general procedure in Scheme 9, substituting l-methyl-piperidine-4-carbonyl chloride (prepared in situ from the corresponding acid using oxalyl chloride) for cyclopentanecarbonyl chloride. *H NMR (300 MHz, DMSO) δ 10.39 (s, IH), 8.64 (dd, TTT), 8.29 (dd, IH), 8.14 (d, IH), 8.05 (d, IH), 7.891 (d, IH), 7.72 (m, TTT), 3.62 (d, 2H), 3.40 (m, 2H), 3.15 (m, IH), 2.95 (m, 2H), 2.78-2.67 (m, 6H), 2.17 (t, 2H), 2.09 (m, 2H), 2.0 (m, 2H), 1.84 (m, IH), 1.43 (m, 2H), 1.39 (m, IH), 1.18 (m, 2H), 0.82 (t, 3H). LC/MS m/z 501 (M + H)+
Figure imgf000143_0001
N-[4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthaIen-l-yI]-2-methyl- nicotinamide (D-25)
The title compound was prepared following the general procedure in Scheme 5, beginning with 4- [(2-methyl-pyridine-3 -carbonyι)-amino] -naphthalene- 1 -sulfonyl chloride, and substituting butyryl chloride and triethylamine for 2-isocyanato- propane. 1H ΝMR (300 MHz, DMSO) δ 10.76 (s, IH), 8.68 (d, IH), 8.59 (d, IH), 8.31 (d, IH), 8.24 (d, IH), 8.10 (d, IH), 8.04 (d, IH), 7.98 (d, IH), 7.73 (m, 2H), 7.41 (m, IH), 4.00 (d, IH), 3.61 (d, IH), 3.23 (m, IH), 2.93 (t, IH), 2.66 (s, 3H), 2.59 (m, IH), 2.17 (t, 2H), 1.48 (m, 2H), 1.43 (m, 2H), 1.19 (m, 2H), 0.82 (m, 2H). LC/MS m/z 494 (M - TT) , 496 (M + H)+
Scheme 10
Figure imgf000143_0002
Figure imgf000144_0001
2-Methyl-N-(5,6,7,8-tetrahydro-naphthalen-l-yl)-benzamide (22) To a 25 °C solution of aniline (1 eq) in anhydrous THF (2 mL per mmol aniline), was added polymer bound pyridine (1.5 eq) followed by acid chloride (1 eq). The mixture was stirred at 25 °C for 12 - 24 h. The reaction mixture was filtered and the filtrate concentrated in vacuo. Hexane or MeOH was added to the residue and the resulting precipitate was collected by filtration, resulting in a white solid (yield 65%). LC/MS (M + H)+ m/z 266. The crude material was used without further purification.
Figure imgf000144_0002
4-(2-Methyl-benzoyIamino)-5,6,7,8-tetrahydro-naphthalene-l-sulfonic acid (23) To a 0°C solution of amide (22) in TFA (1 mL per mmol amide), was added chlorosulfonic acid (2 eq) dropwise under nitrogen atmosphere. The temperature was allowed to warm to 25°C and stirred for 72 hours. The reaction mixture was quenched by pouring into ice water. The desired product was collected via precipitation from either water/methanol, or ethyl acetate/methanol solution, resulting in a white solid (yield 68%). LC/MS (M + H)+ m/z 346, (M - H)" m/z 344. The crude material was used without further purification.
Figure imgf000144_0003
4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthalene-l-sulfonyI chloride (24) Method A: To a 0°C solution of sulfonic acid (23) in DMF (1 mL per mmol acid), was added thionyl chloride (1.1 eq.) dropwise under nitrogen atmosphere. The temperature was allowed to warm to 25°C and stirred for 18 hours. The reaction mixture was quenched by pouring into ice water and filtered to give the title compound as a white solid.
Method B: To neat amide (22), at 0°C, was added chlorosulfonic acid (5 eq) dropwise. The temperature was allowed to warm to 25 °C and then heated at 70°C for 45 minutes. After cooling to 25 °C, the reaction mixture was poured into ice water, and the resultant precipitate was collected by filtration to give the title sulfonyl chloride as a white solid. The product was used without further purification.
Figure imgf000145_0001
2-Methyl-N-[4-(piperidin-4-ylsulfamoyI)-5,6,7,8-tetrahydro-naphthalen-l-yl]- benzamide (26)
To a 25°C solution of sulfonyl chloride (24) (1.61 g, 4 mmol) in THF (60 mL) was added 4-amino-piperidine-l -carboxylic acid tert-butyl ester (880 mg, 4.4 mmol), and followed by triethyl amine (668 mg, 6.6 mmol). The resultant solution was stirred at 25 °C for 18 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo to afford 25. 4 Ν HCl/Dioxane was added and this mixture was stirred for 2 hours, followed by filtration to collect a light gray solid (1.7 g, yield 75%) as the HCl salt of the title compound. LC/MS (M + H)+ m/z 527.
Figure imgf000145_0002
N-[4-(l-Butyryl-piperidin-4-yIsuIfamoyl)-5,6,7,8-tetrahydro-naphthaIen-l-yI]- 2-methyl-benzamide (E-l) To a 25°C mixture of sulfonamide (26) (134 mg, 0.29 mmol) in THF (10 mL) was added butyryl chloride (77 mg, 0.725 mmol) and triethylamine (367 mg, 3.625 mmol). The mixture was stirred for 18 hours, followed by filtration to remove the precipitate. The filtrate was concentrated in vacuo and purified via chromatography, resulting in the title compound as white solid (50 mg). H NMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.55 (m, 2H), 7.41 (m, IH), 7.31 (m, 2H), 4.30 (m, IH), 3.89 (m, IH), 3.21 (m, 2H), 3.09 (m, IH), 2.85 (m, 2H), 2.61 (m, IH), 2.55 (s, 3H), 2.34 (t, 2H), 1.88 (m, 7H), 1.62 (m, TTT), 1.39 (m, TTT), 0.95 (t, 3H) ); LC/MS (M + H)+ m/z 498.
Figure imgf000146_0001
N-(4-CyclohexylsulfamoyI-5,6,7,8-tetrahydro-naphthalen-l-yl)-benzamide (E-2)
The title compound was made following general procedure in Scheme 10, substituting benzoyl chloride for 2-methyl-benzoyl chloride, and cyclohexylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. XTL ΝMR (300 MHz, • CDC13) δ 8.19 (d, IH), 7.95 (d, IH), 7.89 (m, 2H), 7.82 (br s, IH, ΝH), 7.53 (m, 3H), 3.90 (m, IH), 3.20 (t, 2H), 2.72 (t, 2H), 1.52 (m, 14H); LC/MS (M + H)+ m/z 413.
Figure imgf000146_0002
N-[4-(4-Methoxy-phenylsulfamoyl)-5,6,7,8-tetrahydro-naphthaIen-l-yI]- benzamide (E-3)
The title compound was made following general procedure in Scheme 10, substituting benzoyl chloride for 2-methyl-benzoyl chloride, and 4-methoxy- phenylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, CDCI3) δ 8.10 (d, IH), 7.84 (m, 4H), 7.55 (m, 3H), 6.96 (dd, 2H), 6.74 (dd, 2H), 6.64 (br s, IH, N-H), 3.73 (s, 3H), 3.19 (t, 2H), 2.70 (t, 2H), 1.82 (m, 4H); LC/MS (M + H)+ m/z 437.
Figure imgf000147_0001
4-(4-Benzoylamino-5,6,7,8-tetrahydro-naphthalene-l-suIfonyIamino)- piperidine-1-carboxylic acid ethyl ester (E-4)
The title compound was made following general procedure in Scheme 10, substituting benzoyl chloride for 2-methyl-benzoyl chloride, and ethyl chlorofomate for butyryl chloride. 'H ΝMR (300 MHz, CDC13) δ 8.15 (d, IH), 7.94 (d, IH), 7.89 (m, 2H), 7.53 (m, 3H), 4.70 (m, IH), 4.08 (q, TTT), 3.92 (m, 2H), 3.32 (m, IH), 3.15 (m, 2H), 2.76 (m, 4H), 1.80 (m, 4H), 1.36 (m, 3H), 1.22 (t, 3H); LC/MS (M + H)+ m/z 486.
Figure imgf000147_0002
Cyclohexanecarboxylic acid (4-cyclohexylsulfamoyl-5,6,7,8-tetrahydro- naphthalen-l-yl)-amide (E-5)
The title compound was made following general procedure in Scheme 10, substituting cyclohexanecarbonyl chloride for 2-methyl-benzoyl chloride, and cyclohexylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 'H ΝMR
(300 MHz, CDC13) δ 8.00 (d, IH), 7.84(d, IH), 4.24 (m, TTT), 3.11 (m, 3H), 2.57 (m,
2H), 2.22 (m, IH), 2.02 (m, 2H), 1.79 (m, 9H), 1.66 (m, 3H), 1.17 (t, 9H); LC/MS
(M + H)+ m/z 419.
Figure imgf000148_0001
4-(4-(Cyclohexanecarbonyl-amino)-5,6,7,8-tetrahydro-naphthaIene-l- sulfonylamino)-piperidine-l-carboxylic acid ethyl ester (E-6)
The title compound was made following general procedure in Scheme 10, substituting cyclohexanecarbonyl chloride for 2-methyl-benzoyl chloride, and ethyl chlorofomate for butyryl chloride. 'H NMR (300 MHz, MeOD) δ 7.93 (d, IH), 7.51 (d, IH), 4.19 (q, 2H), 4.08 (m, 2H), 3.32 (m, 2H), 3.05 (m, 2H), 2.96 (m, 2H), 2.60 (m, IH), 1.66 (m, 19H), 1.22 (t, 3H); LC/MS (M + H)+ m/z 492.
Figure imgf000148_0002
4-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthaIene-l- sulfonylamino] -piper idine-1 -carboxylic acid ethyl ester (E-8) The title compound was made following general procedure in Scheme 10, substituting ethyl chlorofomate for butyryl chloride. JH NMR (300 MHz, MeOD) δ 7.89 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.29 (m, 2H), 4.22 (q, 2H), 3.92 (m, TTT), 3.21 (m, 3H), 2.81 (m, 4H), 2.49(s, 3H), 1.81 (m, 4H), 1.70(m, 2H), 1.39 (m, 2H), 1.21 (t, 3H); LC/MS (M + H)+ m/z 500.
Figure imgf000148_0003
N-(4-CyclohexyIsulfamoyl-5,6,7,8-tetrahydro-naphthalen-l-yI)-2-methyl- benzamide (E-9)
The title compound was made following general procedure in Scheme 10, substituting cyclohexylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, MeOD) δ 7.92 (d, IH), 7.57 (m, 2H), 7.43 (m, IH), 7.34 (m, 2H), 3.25 (m, 2H), 3.03 (m, IH), 2.88 (m, 2H), 2.45 (s, 3H), 1.88 (m, 4H), 1.78 (m, 5H), 1.22 (m, 5H); LC/MS (M + H)+ m/z 427.
Figure imgf000149_0001
4-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid dimethylamide (E-10)
The title compound was made following general procedure in Scheme 10, substituting dimethylcarbamyl chloride for butyryl chloride. 1H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.54 (m, 2H), 3.21 (m, 4H), 2.81 (m, 4H), 2.79 (s, 6TT), 2.50 (s, 3H), 1.77(m, 3H), 1.71 (m, 2H), 1.45 (m, 2H) ); LC/MS (M + H)+ m/z 499.
Figure imgf000149_0002
2-Methyl-N-{4-[l-(pyrrolidine-l-carbonyI)-piperidin-4-yIsulfamoyI]-5,6,7,8- tetrahydro-naphthalen-l-yl}-benzamide (E-ll)
The title compound was made following general procedure in Scheme 10, substituting pyrrolidine-1 -carbonyl chloride for butyryl chloride. !H ΝMR (300 MHz, MeOD) δ 8.07 (d, IH), 7.69 (m, 2H), 7.55 (m, TTT), 7.48 (m, 2H), 3.79 (m, 2H), 3.46 (m, 4H), 2.91 (m, 4H), 2.61 (s, 3H), 1.98 (m, lOH), 1.85 (m, TTT), 1.61 (m, 3H) ); LC/MS (M + H)+ m/z 525.
Figure imgf000149_0003
N-[4-(l-IsobutyryI-piperidin-4-ylsulfamoyl)-5,6,7,8-tetrahydro-naphthaIen-l- yl]-2-methyl-benzamide (E-12)
The title compound was made following general procedure in Scheme 10, substituting isobutyryl chloride for butyryl chloride. 'H ΝMR (300 MHz, MeOD) δ 7.95 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.29 (m, 2H), 4.29 (m, IH), 3.89 (m, IH), 3.19 (m, 3H), 2.85 (m, 3H), 2.47 (s, 3H), 1.82 (m, 7H), 1.38 (m, 3H), 1.09 (m, 6H);
LC/MS (M + TT m/z 498.
Figure imgf000150_0001
naphthalen-l-yI]-2-methyI-benzamide (E-13)
The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester. 'H ΝMR (300 MHz, MeOD) δ 7.88 (d, IH), 7.50 (m, 2H), 7.35 (m, IH), 7.25 (m, ITT), 3.71 (m, 2H), 3.44 (m, 2H), 3.21 (m, 3H), 2.82 (s, 2H), 2.47 (s, 3H), 2.30 (m, 2H), 1.81 (m, 5H), 1.60 (m, 2H), 0.83 (d, 3H) ); LC MS (M + H)+ m/z 532.
Figure imgf000150_0002
4-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthaIene-l- sulfony!amino]-piperidine-l-carboxylic acid diethylamide (E-14)
The title compound was made following general procedure in Scheme 10, substituting diethylcarbamyl chloride for butyryl chloride. XH ΝMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.51 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.50 (m, 2H), 3.20 (m, 4H), 3.18 (q, ATT), 2.80 (m, 4H), 2.50 (s, 3H), 1.85 (m, 3H), 1.73 (m, 2H), 1.49 (m, 2H), 1.11 (t, 6H) ); LC/MS (M + H)+ m/z 527.
Figure imgf000150_0003
4-[4-(2-Methyl-benzoyIamino)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid methyl ester (E-15) The title compound was made following general procedure in Scheme 10, substituting methyl chlorofomate for butyryl chloride. *H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.92 (m, 2H), 3.63 (s, 3H), 3.20 (m, 4H), 2.85 (m, 4H), 2.50 (s, 3H), 1.85 (m, 3H), 1.72 (m, 2H), 1.41 (m, 2H) ); LC MS (M + H)+ m/z 486.
Figure imgf000151_0001
4-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid isopropyl ester (E-16) The title compound was made following general procedure in Scheme 10, substituting isopropyl chlorofomate chloride for butyryl chloride. *H NMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.56 (m, 2H), 7.40 (m, IH), 7.31 (m, 2H), 3.92 (m, 2H), 3.26 (m, IH), 3.21 (m, 4H), 2.83 (m, 4H), 2.50 (s, 3H), 1.85 (m, 3H), 1.72 (m, 2H), 1.39 (m, 2H), 1.20 (d, 6H) ); LC/MS (M + H)+ m/z 514.
Figure imgf000151_0002
N-{4-[l-(2-Dimethylamino-acetyl)-piperidin-4-ylsulfamoyl]-5,6,7,8-tetrahydro- naphthaIen-l-yl}-2-methyl-benzamide (E-17)
The title compound was made following general procedure in Scheme 10, substituting dimethylamino-acetyl chloride for butyryl chloride. *H ΝMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.56 (m, 2H), 7.40 (m, IH), 7.31 (m, 2H), 4.28 (m, IH), 3.93 (d, 2H), 3.66 (m, IH), 3.25 (m, 4H), 2.80 (m, 4H), 2.72 (s, 6H), 2.51 (s, 3H), 1.85 (m, 5H), 1.45 (m, 2H) ); LC/MS (M + H)+ m/z 513.
Figure imgf000151_0003
N-{4-[l-(2-Methoxy-acetyl)-piperidin-4-ylsulfamoyl]-5,6,7,8-tetrahydro- naphthalen-l-yl}-2-methyl-benzamide (E-18) The title compound was made following general procedure in Scheme 10, substituting methoxy-acetyl chloride for butyryl chloride. H NMR (300 MHz, MeOD) δ 7.92 (d, IH), 7.56 (m, 2H), 7.41 (m, IH), 7.35 (m, TTT), 4.25 (m, IH), 4.12 (d, TTT), 3.73 (m, IH), 3.36 (s, 3H), 3.26 (m, 4H), 3.02 (m, IH), 2.80 (m, 3H), 2.49 (s, 3H), 1.84 (m, 5H), 1.40 (m, 2H) ); LC/MS (M + H)+ m/z 500.
Figure imgf000152_0001
4-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthaIene-l- sulfonylamino]-piperidine-l-carboxylic acid ethylamide (E-19) The title compound was made following general procedure in Scheme 10, substituting isocyanato-ethane for butyryl chloride. 1H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.55 (m, 2H), 7.41 (m, IH), 7.31 (m, 2H), 3.83 (m, 2H), 3.24 (m, 4H), 3.14 (q, 2H), 2.79 (m, 4H), 2.50 (s, 3H), 1.84 (m, 3H), 1.70 (m, TTT), 1.38 (m, 2H), 1.07 (t, 3H) ); LC/MS (M + H)+ m/z 499.
Figure imgf000152_0002
(±)-cw-3-MethyI-4-[4-(2-methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthalene- l-sulfonylamino]-piperidine-l-carboxylic acid dimethylamide (E-20)
The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. 1H NMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.55 (m, TTT), 7.39 (m, IH), 7.31 (m, 2H), 3.36 (m, 2H), 3.22 (m, 2H), 3.10 (m, 3H ), 2.82 (m, 2H), 2.80 (s, 6H), 2.49 (s, 3H), 1.85 (m, 5H), 1.65 (m, IH), 1.51 (m, IH), 0.82 (d, 3H) ); LC/MS (M + H)+ m/z 513.
Figure imgf000152_0003
(±)-cw-3-Methyl-4-[4-(2-methyI-benzoylamino)-5,6,7,8-tetrahydro-naphthalene- l-sulfonylamino]-piperidine-l-carboxyIic acid ethyl ester (E-21)
The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester, and ethyl chlorofomate for butyryl chloride. !H NMR (300 MHz, MeOD) δ 7.92 (d, IH), 7.58 (m, 2H), 7.41 (m, IH), 7.35 (m, TTT), 4.12 (q, 2H), 3.71 (m, IH), 3.29 (m, 6TT), 2.88 (m, 2H), 2.52 (s, 3H), 1.88 (m, 5H), 1.62 (m, IH), 1.51 (m, IH), 1.25 (t, 3H), 0.89 (d, 3H) ); LC/MS (M + H)+ m/z 514.
Figure imgf000153_0001
4-[4-(2-MethyI-benzoyIamino)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxy!ic acid methylamide (E-22) The title compound was made following general procedure in Scheme 10, substituting isocyanato-methane for butyryl chloride. *H NMR (300 MHz, MeOD) δ 7.93 (d, IH), 7.59 (m, 2H), 7.43 (m, IH), 7.36 (m, TTT), 3.88 (m, TTT), 3.29 (m, 4H), 2.83 (m, 4H), 2.71 (s, 3H), 2.54 (s, 3H), 1.88 (m, 3H), 1.73 (m, 2H), 1.41 (m, 2H) ); LC/MS (M + TT)+.m/z 486.
Figure imgf000153_0002
2-Methyl-N-[4-(tetrahydro-pyran-4-ylsulfamoyl)-5,6,7,8-tetrahydro- naphthalen-l-yl]-benzamide (E-23)
The title compound was made following general procedure in Scheme 10, substituting tetrahydro-pyran-4-ylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.54 (m, 2H), 7.39 (m, IH), 7.32 (m, 2H), 3.84 (m, 2H), 3.29 (m, 6H), 2.83 (m, 2H), 2.51 (s, 3H), 1.88 (m, 3H), 1.69 (m, 2H), 1.54 (m, 2H) ); LC/MS (M + H)+ m/z 429.
Figure imgf000154_0001
2-Methyl-N-{4-[3-(2-oxo-pyrrolidin-l-yl)-propyIsulfamoyl]-5,6,7,8-tetrahydro- naphthalen-l-yl}-benzamide (E-24)
The title compound was made following general procedure in Scheme 10, substituting l-(3-amino-propyl)-pyrrolidin-2-one for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester. XH ΝMR (300 MHz, MeOD) δ 7.80 (d, IH), 7.50 (t, 2H), 7.37 (m, IH), 7.29 (m, 2H), 3.34(t, TTT), 3.21 (t, TTT), 3.17 (m, 2H), 2.86 (t, 2H), 2.79 (m, 2H), 2.46 (s, 3H), 2.31 (t, 2H), 1.98 (m, 2H), 1.82 (m, 4H), 1.65 (m, 2H) ); LC/MS (M + H)+ m/z 470.
Figure imgf000154_0002
2-Methyl-N-[4-(3-morpholin-4-yl-propylsulfamoyI)-5,6,7,8-tetrahydro- naphthalen-l-y!]-benzamide (E-25)
The title compound was made following general procedure in Scheme 10, substituting 3 -morpholin-4-yl-propylamine for 4-amino-piperidine- 1 -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, MeOD) δ 7.83 (d, IH), 7.54 (t, 2H), 7.41 (m, IH), 7.31 (m, 2H), 3.74(m, 4H), 3.19 (m, 2H), 2.98 (t, 2H), 2.75 (m, 8H), 2.49 (s, 3H), 1.81 (m, 6H) ); LC/MS (M + H)+ m/z 472.
Figure imgf000154_0003
N-(4-CyclopentyIsuIfamoyl-5,6,7,8-tetrahydro-naphthalen-l-yl)-2-methyI- benzamide (E-26)
The title compound was made following general procedure in Scheme 10, substituting cyclopentylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. 1H ΝMR (300 MHz, MeOD) δ 7.88 (d, IH), 7.54 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.49 (m, IH), 3.21 (m, 2H), 2.72 (m, TTT), 2.50 (s, 3H), 1.83 (m, 4H), 1.69 (m, 4H), 1.48 (m, 4H); LC/MS (M + H)+ m/z 413.
Figure imgf000155_0001
N-[4-(Cyclohexylmethyl-sulfamoyl)-5,6,7,8-tetrahydro-naphthalen-l-yl]-2- methyl-benzamide (E-27)
The title compound was made following general procedure in Scheme 10, substituting C-cyclohexyl-methylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. Η ΝMR (300 MHz, MeOD) δ 7.82 (d, IH), 7.54 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.21 (m, TTT), 2.83 (m, 2H), 2.69 (d, 2H), 2.49 (s, 3H), 1.83 (m, 3H), 1.69 (m, 6H), 1.39 (m, IH), 1.19 (m, 3H), 0.85 (m, 2H) ); LC/MS (M + H)+ m/z 441.
Figure imgf000155_0002
(±)-2-Methyl-N-[4-(piperidin-3-ylsulfamoyl)-5,6,7,8-tetrahydro-naphthalen-l- yl]-benzamide (E-28)
The title compound was made following general procedure in Scheme 10, substituting (R, S)-3 -amino-piperidine-1 -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester. *H ΝMR (300 MHz, MeOD) δ 7.91 (d, IH), 7.57 (m, 2H), 7.41 (m, IH), 7.33 (m, 2H), 3.23 (m, 4H), 3.11 (m, IH), 2.85 (m, 2H), 2.70(m, 2H), 2.50 (s, 3H), 1.73 (m, 6TT), 1.54 (m, 2H) ); LC/MS (M + H)+ m/z 428.
Figure imgf000155_0003
(±)-2-MethyI-N-[4-(pyrrolidin-3-yIsulfamoyI)-5,6,7,8-tetrahydro-naphthaIen-l- yl]-benzamide (E-29) The title compound was made following general procedure in Scheme 10, substituting (R, S)-3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester. *H NMR (300 MHz, MeOD) δ 7.89 (d, IH), 7.57 (m, 2H), 7.41 (m, IH), 7.33 (m, 2H), 3.81 (m, IH), 3.22 (m, 7H), 2.84 (m, 2H), 2.50 (s, 3H), 2.09 (m, IH), 1.83 (m, 4H) ); LC/MS (M + H)+ m/z 414.
Figure imgf000156_0001
(±)-3-[4-(2-Methyl-benzoyIamino)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid dimethylamide (E-30) The title compound was made following general procedure in Scheme 10, substituting (R, S)-3 -amino-piperidine-1 -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. *H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.56 (m, 2H), 7.39 (m, IH), 7.31 (m, TTT), 3.40 (m, 3H), 3.15 (m, 3H), 2.85 (m, 2H), 2.74 (s, 6H), 2.69(m, 2H), 2.50 (s, 3H), 1.73 (m, 4H), 1.69 (m, IH), 1.44 (m, 2H) ); LC/MS (M + H)+ m/z 499.
Figure imgf000156_0002
(±)-3-[4-(2-Methyl-benzoylamirio)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxylic acid ethyl ester (E-31)
The title compound was made following general procedure in Scheme 10, substituting (R, S)-3 -amino-piperidine-1 -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester, and ethyl chlorofomate for butyryl chloride. 'H NMR (300 MHz, MeOD) δ 7.92 (d, IH), 7.59 (m, 2H), 7.42 (m, IH), 7.34 (m, 2H), 4.09 (q, 2H), 3.91 (m, IH), 3.79 (m, IH), 3.24 (m, 2H), 3.09 (m, 2H), 2.85 (m, 4H), 2.51 (s, 3H), 1.86 (m, 4H), 1.71 (m, IH), 1.42 (m, 2H), 1.23 (t, 3H) ); LC/MS (M + H)+ m/z 500.
Figure imgf000157_0001
(±)-3-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthaIene-l- sulfonylamino]-pyrrolidine-l-carboxyIic acid dimethylamide (E-32) The title compound was made following general procedure in Scheme 10, substituting (R,S)-3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. 'H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.57 (m, TTT), 7.41 (m, IH), 7.32 (m, 2H), 3.78 (m, IH), 3.48 (m, IH), 3.28 (m, 2H), 3.18 (m, 3H), 2.84 (m, 3H), 2.78 (s, 6H), 2.50 (s, 3H), 1.96 (m, IH), 1.82 (m, 4H) ); LC/MS (M + H)+ m/z 485.
Figure imgf000157_0002
(±)-3-[4-(2-Methyl-benzoylamino)-5,6,7,8-tetrahydro-naphthalene-l- su!fonylamino]-pyrrolidine-l-carboxylic acid ethyl ester (E-33) The title compound was made following general procedure in Scheme 10, substituting (R, S)-3-amino-pyrrolidine-l -carboxylic acid tert-butyl ester for 4- amino-piperidine-1 -carboxylic acid tert-butyl ester, and ethyl chlorofomate for butyryl chloride. 1H NMR (300 MHz, MeOD) δ 7.89 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.30 (m, 2H), 4.09 (m, 2H), 3.79 (m, IH), 3.41 (m, 3H), 3.18 (m, ATT), 2.82 (m, 2H), 2.50 (s, 3H), 1.99 (m, IH), 1.89 (m, ATT), 1.22 (m, 3H) ); LC/MS (M + H)+ m/z 486.
Figure imgf000157_0003
(±)-trfln*-3-MethyI-4-[4-(2-methyI-benzoylamino)-5,6,7,8-tetrahydro- naphthalene-l-sulfonylamino]-piperidine-l-carboxylic acid dimethylamide (E-
34) The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. LC/MS (U + TT)+ m/z 513.
Figure imgf000158_0001
(3R, ¥S -3-Methyl-4-[4-(2-methyl-benzoylamino)-5,6,7,8-tetrahydro- naphthalene-l-suIfonylamino]-piperidine-l-carboxylic acid dimethylamide (E-
35) The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. Compound E-20 was prepared as described previously, and the enantiomers were separated via chiral HPLC chromatography of E-35; the title compound eluted as peak 1. !H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.36 (m, 2H), 3.22 (m, 2H), 3.10 (m, 3H), 2.82 (m, TTT), 2.80 (s, 6H), 2.49 (s, 3H), 1.85 (m, 4H), 1.65 (m, IH), 1.49 (m, IH), 0.83 (d, 3H) ); LC/MS (M + H)+ m/z 537.
Figure imgf000158_0002
(3S, 4R) - 3-MethyI-4-[4-(2-methyI-benzoylamino)-5,6,7,8-tetrahydro- naphthalene-l-su!fonylamino]-piperidine-l-carboxylic acid dimethylamide (E-
36)
The title compound was made following general procedure in Scheme 10, substituting 1 -benzyl-3 -methyl-piperidin-4-ylamine for 4-amino-piperidine- 1- carboxylic acid tert-butyl ester, and dimethylcarbamyl chloride for butyryl chloride. Compound E-20 was prepared as described previously, and the enantiomers were separated via chiral HPLC chromatography of E-35; the title compound eluted as peak 2. 1H NMR (300 MHz, MeOD) δ 7.90 (d, IH), 7.55 (m, 2H), 7.39 (m, IH), 7.31 (m, 2H), 3.36 (m, 2H), 3.22 (m, 2H), 3.10 (m, 3H), 2.82 (m, 2H), 2.80 (s, 6H), 2.49 (s, 3H), 1.85 (m, 4H), 1.65 (m, IH), 1.49 (m, IH), 0.83 (d, 3H) ); LC/MS (M + H)+ m/-. 513.
Scheme 11
Figure imgf000159_0001
4-FIuoro-naphthalene-l-sulfonyl chloride (27)
1-Fluoronaphthalene (20.0 g, 0.14 mol) was added in small portions to a stirred solution of chlrosulfonic acid (79 g, 45 mL, 0.68 mol) at room temperature. The reaction was stirred for 30 minutes until gas evolution ceased. The reaction mixture was poured carefully over a mixture of ice (300 g) and dichloromethane (300 mL) and charged to a separatory funnel. The organic layer was separated, washed twice with water and brine and dried over MgS0 . Filtration and concentration in vacuo afforded 27 as a tan solid. Wt.: 27.6 g (82%). 'H NMR (300 MHz, CDC13) δ 8.79 (dd, IH), 8.38 (dd, IH), 8.28 (d, IH), 7.88 (m, IH), 7.77 (m, IH), 7.26 (dd, IH).
Figure imgf000160_0001
4-(4-Fluoro-naphthalene-l-sulfonylamino)-piperidine-l-carboxylic acid tert- butyl ester (28)
4-Fluoro-naphthalene-l -sulfonyl chloride 27 (10.0 g, 40.9 mmol) was dissolved in THF (100 mL) and stirred at room temperature. 4- Amino-piperidine-1 -carboxylic acid tert-butyl ester (8.19 g, 40.9 mmol) and triethylamine (4.14 g, 5.75 mL, 40.9 mmol) were added and the reaction was stirred overnight at room temperature. The solvent was removed in vacuo. Dichloromethane (250 mL) was added and the solution was charged to a separatory funnel. The organic layer was washed twice with water and brine and dried over MgS04. Filtration and concentration in vacuo afforded 28 as a yellow foam. Wt.: 15.1 g (90%). 1H NMR (300 MHz, CDC13) δ 8.62 (d, IH), 8.26 (m, 2H), 7.69 (m, 2H), 7.20 (m, IH), 4.92 (d, IH), 3.82 (m, 2H), 3.26 (m, IH), 2.70 (m, TTT), 1.61 (m, 2H), 1.40 (s, 9H), 1.24 (m, 2H); LC/MS m/z 409 (M + H)+.
Figure imgf000160_0002
4-(4-Cyano-naphthalene-l-sulfonyIamino)-piperidine-l-carboxylic acid tert- butyl ester (29)
4-(4-Fluoro-naphthalene-l -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester 28 (2.00 g, 4.9 mmol) was dissolved in DMF (20 mL). Sodium cyanide (1.2 g, 24.5 mmol) and tetra-π-butylammonium bromide (7.9 g, 24.5 mmol) were added and the reaction was heated to 100°C overnight. The reaction was diluted with dichloromethane (100 mL) and charged to a separatory funnel. The organic layer was washed three times with water, brine and dried over MgS0 . Filtration and concentration in vacuo afforded a dark colored oil. Flash column chromatography (98:2 dichloromethane :methanol) afforded an oil that was rechromatographed (99:1 dichloromethane :methanol) to afford 29 as an orange solid. Wt.: 640 mg (31%). *H NMR (300 MHz, CDC13) δ 8.71 (m, IH), 8.40 (m, IH), 8.34 (d, IH), 8.00 (d, IH), 7.83 (m, TTT), 4.80 (d, IH), 3.87 (m, 2H), 3.32 (m, IH), 2.61 (m, 2H), 1.63 (m, 2H), 1.38 (s, 9TT), 1.27 (m, 2H); LC/MS m/z 414 (M - HV
Figure imgf000161_0001
4-(4-Carboxy-naphthaIene-l-suIfonylamino)-piperidine-l-carboxylic acid tert- butyl ester (30)
4-(4-Cyano-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester 29 (0.48 g, 1.15 mmol) was dissolved in a mixture of aqueous potassium hydroxide (20 mL, 1.8N, 36 mmol) and isopropanol (25 mL). The mixture was heated to 75°C for two days. LC/MS analysis showed a mixture of starting material, carboxylic acid and amide. The isopropanol was removed in vacuo and the aqueous layer was extracted with ethyl acetate and the organic layer discarded. The aqueous layer was acidified to pH 3 and extracted with ethyl acetate. The organic layer washed with water, then brine and dried over MgSO4. Filtration and concentration in vacuo afforded 30 as a tan colored foam. Wt.: 360 mg (72%). 'H NMR (300 MHz, CDC13) δ 9.03 (m, IH), 8.70 (m, IH), 8.33 (dd, 2H), 7.74 (m, 2H), 4.78 (d, IH), 3.85 (m, 2H), 3.31 (m, IH), 2.71 (m, 2H), 1.62 (m, 2H), 1.40 (s, 9H), 1.27 (m, 2H); LC/MS m/z 433 (M - H)_.
Figure imgf000162_0001
4-(4-CyclohexylcarbamoyI-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid tert-butyl ester (F-l)
4-(4-Carboxy-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester 5 (400 mg, 0.92 mmol) was dissolved in dichloromethane (5 mL). l-[3-
(Dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDCI) (350 mg, 1.84 mmol), 1-hydroxybenzotriazole (186 mg, 1.38 mmol), triethylamine (280 mg, 0.38 mL, 2.76 mmol) and cyclohexylamine (0.14 g, 0.16 mL, 1.38 mmol) were added and the reaction was stirred overnight at room temperature. The reaction was diluted with dichloromethane (30 mL) and charged to a separatory funnel. The organic layer was washed twice with water and brine and dried over Na2S0 . Filtration and concentration in vacuo afforded a foam that was purified via flash column chromatography (98:2 dichloromethane :methanol) to give the title compound. Wt.: 320 mg (68%). 1H NMR (300 MHz, CDC13) δ 8.61 (m, IH), 8.31 (m, IH), 8.26 (d, IH), 7.68 (m, 2H), 7.59 (d, IH), 5.91 (d, IH), 4.64 (d, IH), 4.12 (m, IH), 3.82 (m, 2H), 3.22 (m, IH), 2.68 (m, 2H), 2.13 (m, 2H), 1.79 (m, 2H), 1.57 (m, 6H), 1.38 (s, 9H), 1.27 (m, 4H); LC/MS m/z 516 (M + H)+.
Figure imgf000162_0002
4-(Piperidin-4-ylsuIfamoyl)-naphthalene-l-carboxyIic acid cyclohexylamide (F-
2) 4-(4-Cyclohexylcarbamoyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester F-l (320 mg, 0.62 mmol) was dissolved in 4N HCl/dioxane (10 mL). The reaction was stirred for 2 hours at room temperature and concentrated in vacuo to afford the title compound as its hydrochloride salt. Wt.: 271 mg (97%) *H NMR (300 MHz, d°-DMSO) δ 8.68 (d, IH), 8.59 (d, IH), 8.40 (d, IH), 8.15 (m, 2H), 7.72 (m, 2H), 7.60 (d, IH), 3.75 (m, IH), 3.67 (m, IH), 3.08 (m, 2H), 2.80 (m, 2H), 2.54 (m, IH), 1.92 (m, 2H), 1.74 (m, 2H), 1.62 (m, 4H), 1.48 (m, IH), 1.32 (m, ATT), 1.25 (m, IH); LC/MS m/z 416 (M + H)+.
Figure imgf000163_0001
4-(4-Cyclohexylcarbamoyl-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid ethyl ester (F-3)
4-(Piperidin-4-ylsulfamoyl)-naphthalene- 1 -carboxylic acid cyclohexylamide hydrochloride F-2 (87 mg, 0.19 mmol) was dissolved and stirred in dichloromethane (2 mL). Triethylamine (58 mg, 0.08 mL, 0.57 mmol) was added followed by ethyl chloroformate (41 mg, 0.037 mL, 0.39 mmol). The reaction was stirred overnight at room temperature, then charged directly to a flash column. Elution with 99:1 dichloromethane:methanol afforded the titled compound the title compound as a white solid. Wt: 60 mg (65%). 1H NMR (300 MHz, CDC13) δ 8.59 (m, IH), 8.28 (m, IH), 8.19 (d, IH), 7.64 (m, 2H), 7.54 (d, IH), 4.10 (m, IH), 4.03 (q, TTT), 3.80 (m, 2H), 3.64 (m, IH), 3.18 (m, IH), 2.68 (m, 2H), 2.12 (m, 2H), 1.79 (m, 2H), 1.68 (m, IH), 1.58 (m, 2H), 1.47 (m, 2H), 1.24 (m, 6H), 1.18 (t, 3H); LC/MS m/z 488 (M + H)+.
Figure imgf000164_0001
4-(4-ø-Tolylcarbamoyl-naphthalene-l-sulfonyIamino)-piperidine-l-carboxylic acid tert-butyl ester (F-4)
The titled compound was prepared according to the general procedure in Scheme 11, substituting 2-methylphenylamine for cyclohexylamine. Wt.: 337 mg (70%). 1H NMR (300 MHz, CDC13) δ 8.66 (d, IH), 8.46 (d, IH), 8.35 (d, IH), 8.04 (d, IH), 7.80 (m, IH), 7.72 (m, 2H), 7.54 (s, IH), 7.34 (m, IH), 7.21 (m, IH), 4.16 (d, IH), 3.85 (m, 2H), 3.27 (m, IH), 2.70 (m, 2H), 2.34 (s, 3H), 2.23 (m, IH), 1.66 (m, 2H), 1.56 (m, 4H), 1.40 (s, 9H), 1.27 (m, 4H); LC/MS m/z 524 (M + H)+.
Figure imgf000164_0002
4-[4-(2,3-Dimethyl-phenylcarbamoyI)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid tert-butyl ester (F-13)
The titled compound was prepared according to the general procedure in Scheme 11, substituting 2,3-dimethyl-phenylamine for cyclohexylamine. Wt.: 353 mg (75%). 'H NMR (300 MHz, CDC13) δ 8.66 (m, IH), 8.47 (d, IH), 8.35 (d, IH), 7.81 (d, IH), 7.72 (m, 2H), 7.54 (s, IH), 7.22 (m, TTT), 7.13 (m, IH), 4.63 (d, IH), 3.86 (m, 2H), 3.27 (m, IH), 2.70 (m, 2H), 2.35 (s, 3H), 2.24 (s, 3H), 1.64 (m, 2H), 1.34 (m, 2H); LC/MS m/z 537 (M - H)\
Figure imgf000165_0001
4-[4-(2-Chloro-phenylcarbamoyl)-naphthalene-l-suIfonylamino]-piperidine-l- carboxylic acid tert-butyl ester (F-14)
The titled compound was prepared according to the general procedure in Scheme 11, substituting 2-chloro-phenylamine for cyclohexylamine. Wt.: 329 mg (66%). !H NMR (300 MHz, CDC13) δ 8.68 (m, IH), 8.62 (m, IH), 8.46 (d, IH), 8.37 (m, IH), 8.20 (s, IH), 7.83 (d, IH), 7.73 (m, 2H), 7.46 (m, IH), 7.40 (m, IH), 7.17 (m, IH), 4.68 (d, IH), 3.87 (m, 2H), 3.30 (m, IH), 2.62 (m, 2H), 1.68 (m, TTT), 1.40 (s, 9H), 1.26 (m, 2H); LC/MS m/z 543 (M - H)".
Figure imgf000165_0002
4-[4-(Tetrahydro-pyran-4-ylcarbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid tert-butyl ester (F-15)
The title compound was prepared according to the general procedure in Scheme 11, substituting tetrahydro-pyran-4-ylamine for cyclohexylamine. Wt.: 368 mg (11%). *H NMR (300 MHz, CDC13) δ 8.60 (m, IH), 8.29 (m, IH), 8.24 (d, IH), 7.68 (m, 2H), 7.59 (d, IH), 6.12 (d, IH), 4.73 (d, IH), 4.34 (m, IH), 4.04 (m, 2H), 3.82 (m, 2H), 3.57 (m, 2H), 3.21 (m, IH), 2.67 (m, 2H), 2.11 (m, IH), 1.62 (m, 3H), 1.36 (s, 9H), 1.20 (m, 4H); LC/MS m/z 516 (M - H)\
Figure imgf000166_0001
4-(4-Phenylcarbamoyl-naphthalene-l-sulfonylamino)-piperidine-l-carboxylic acid tert-butyl ester
The titled compound was prepared according to the general procedure in Scheme 11, substituting phenylamine for cyclohexylamine. Wt.: 66 mg (55%). !H NMR (300 MHz, CDC13) δ 8.62 (d, IH), 8.37 (m, 2H), 8.26 (d, IH), 7.93 (s, IH), 7.70 (m, 4H), 7.43 (m, 3H), 4.76 (d, IH), 3.80 (m, 2H), 3.24 (m, IH), 2.67 (m, 2H), 1.60 (m, 2H), 1.39 (s, 9H), 1.22 (m, TTT); LC/MS m/z 510 (M + H)+.
Figure imgf000166_0002
4-(4-m-ToIylcarbamoyl-naphthalene-l-sulfonylamino)-piperidine-l-carboxyIic acid tert-butyl ester
The title compound was prepared according to the general procedure in Scheme 11, substituting m-tolylamine for cyclohexylamine. Wt.: 61 mg (51%). *H NMR (300 MHz, CDC13) δ 8.62 (d, IH), 8.35 (m, 2H), 8.18 (d, IH), 7.65 (m, 4H), 7.28 (m, 2H), 7.03 (d, IH), 5.13 (d, IH), 3.73 (m, 2H), 3.18 (m, IH), 2.62 (m, 2H), 2.40 (s, 3H), 1.55 (m, 2H), 1.38 (s, 9H), 1.12 (m, TTT); LC/MS m/z 524 (M + H)+.
Figure imgf000167_0001
4-[4-(Cyclohexyl-methyl-carbamoyI)-naphthalene-l-suIfonylamino]-piperidine- 1-carboxylic acid tert-butyl ester
The title compound was prepared according to the general procedure in Scheme 11, substituting cyclohexyl-methyl-amine for cyclohexylamine, and 0-(7- azabenzotriazol-l-yl)-N,NN',N'-tetramethyluronium hexafluorophosphate for EDCI. Wt.: 440 mg (100%). !H ΝMR (300 MHz, CDC13) δ 8.63 (d, IH), 8.31 (d, IH), 7.89 (m, IH), 7.67 (m, 2H), 7.42 (m, IH), 4.77 (s, IH), 3.87 (m, 2H), 3.22 (m, IH), 2.79 (s, 3H), 2.60 (m, 2H), 1.88 (m, 4H), 1.55 (m, 8H), 1.38 (s, 9H), 1.15 (m, TTT); LC/MS m/z 530 (M + H)+.
Figure imgf000167_0002
4-(Piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid o-tolylamide (F-5) The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(4-o-tolylcarbamoyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 275 mg (97%). 1H ΝMR (300 MHz, - -DMSO) δ 10.22 (s, IH), 8.73 (m, IH), 8.44 (m, 2H), 8.30 (m, IH), 8.24 (m, IH), 7.88 (d, IH), 7.77 (m, TTT), 7.52 (d, IH), 7.28 (m, IH), 7.22 (m, IH), 3.11 (m, 2H), 2.83 (m, 2H), 2.53 (m, IH), 2.32 (s, 3H), 1.67 (m, 2H), 1.51 (m, TTT); LC/MS m/z 424 (M + H)+.
Figure imgf000168_0001
4-(Piperidin-4-ylsuIfamoyl)-naphthalene-l-carboxylic acid (2,3-dimethyl- phenyl)-amide (F-16)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-[4-(2,3-dimethyl-phenylcarbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl- naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 312 mg (99%). !H NMR (300 MHz, f-OMSO) δ 10.27 (s, IH), 8.72 (d, IH), 8.47 (d, IH), 8.30 (m, IH), 8.23 (d, IH), 7.90 (d, IH), 7.75 (m, 2H), 7.31 (d, IH), 7.12 (m, 2H), 3.68 (m, IH), 3.10 (m, 2H), 2.80 (m, 2H), 2.30 (s, 3H), 2.20 (s, 3H), 2.02 (m, IH), 1.67 (m, 2H), 1.53 (m, 2H); LC/MS m/z 436 (M - HV.
Figure imgf000168_0002
4-(Piperidin-4-ylsuIfamoyl)-naphthalene-l-carboxyIic acid (2-chIoro-phenyl)- amide (F-17)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-[4-(2-chloro-phenylcarbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl- naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 219 mg (98%). 1H NMR (300 MHz, °-DMSO) δ 10.51 (s, IH), 8.72 (d, IH), 8.52 (m, IH), 8.47 (d, IH), 8.35 (m, IH), 8.24 (d, IH), 7.90 (d, IH), 7.75 (m, 2H), 7.59 (d, IH), 7.43 (m, IH), 7.32 (m, IH), 3.67 (m, IH), 3.08 (m, 2H), 2.82 (m, TTT), 1.65 (m, 2H), 1.50 (m, 2H); LC/MS m/z 442 (M - H)".
Figure imgf000169_0001
4-(Piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid (tetrahydro-pyran- 4-yl)-amide (F-18)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-[4-(tetrahydro-pyran-4-ylcarbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl- naphthalene- l-sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 321 mg (100%). 1H NMR (300 MHz, . -DMSO) δ 8.69 (m, TTT), 8.42 (m, 2H), 8.15 (m, IH), 7.72 (m, 2H), 7.63 (d, IH), 4.08 (m, IH), 3.87 (m, 2H), 3.42 (m, 2H), 3.08 (m, 2H), 2.80 (m, TTT), 1.86 (m, 2H), 1.64 (m 4H), 1.51 (m, 4H); LC/MS m/z 416 (M - H)-.
Figure imgf000169_0002
4-(Piperidin-4-ylsulfamoyl)-naphthaIene-l-carboxylic acid phenylamide
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(4-phenylcarbamoyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 38 mg (61%). LC/MS m/z 410 (M + H)+.
Figure imgf000170_0001
4-(Piperidin-4-yIsulfamoyI)-naphthalene-l-carboxylic acid -tolyIamide
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(4-m-tolylcarbamoyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt. 39 mg (75%). LC/MS m/z 424 (M + H)+.
Figure imgf000170_0002
4-(Piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid cyclohexyl-methyl- amide
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-[4-(cyclohexyl-methyl-carbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1 -carboxylic acid tert-butyl ester for 4-(4-cyclohexylcarbamoyl- naphthalene- l-sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester. Wt.: 440 mg (100%). LC/MS m/z 424 (M + H)+.
Figure imgf000170_0003
4-(4-Cyclohexylcarbamoyl-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid dimethylamide (F-6)
The title compound was prepared according to the general procedure in Scheme 11, substituting dimethylcarbamyl chloride for ethyl chloroformate. Wt.: 56 mg (50%). 1H NMR (300 MHz, CDC13) δ 8.58 (d, IH), 8.30 (d, IH), 8.25 (d, 2H), 7.68 (m, 2H), 7.56 (d, IH), 6.00 (d, IH), 4.77 (d, IH), 4.11 (m, IH), 3.42 (m, 2H), 3.23 (m, IH), 2.71 (s, 6TT), 2.63 (m, 2H), 2.13 (m, 2H), 1.80 (m, 2H), 1.63 (m, 2H), 1.47 (m, 2H), 1.27 (m, 6H); LC/MS m/z 485 (M - H)".
Figure imgf000171_0001
4-(l-Butyryl-piperidin-4-yIsulfamoyI)-naphthalene-l-carboxylic acid cyclohexylamide (F-7)
The title compound was prepared according to the general procedure in Scheme 11, substituting butyryl chloride for ethyl chloroformate. Wt.: 50 mg (47%). *H NMR (300 MHz, CDC13) δ 8.60 (d, IH), 8.32 (d, IH), 8.27 (d, IH), 7.72 (m, 2H), 7.57 (d,
IH), 6.00 (d, IH), 4.78 (d, IH), 4.24 (m, IH), 4.11 (m, IH), 3.64 (m, IH), 3.27 (m,
IH), 2.91 (m, IH), 2.56 (m, IH), 2.15 (m, ATT), 1.62 (m, 8H), 1.25 (m, ATT), 0.95 (m,
2H), 0.88 (t, 3H); LC/MS m/z 484 (M - H)-.
Figure imgf000171_0002
4-(4-Cyclohexylcarbamoyl-naphthalene-l-suIfonylamino)-piperidine-l- carboxylic acid ethylamide (F-8) The title compound was prepared according to the general procedure in Scheme 11, substituting ethyl isocyanate for ethyl chloroformate. Wt.: 56 mg (49%). !H NMR (300 MHz, CDC13) δ 8.60 (d, IH), 8.29 (d, IH), 8.23 (d, IH), 7.68 (m, 2H), 7.57 (d, IH), 6.03 (d, IH), 4.83 (d, IH), 4.30 (m, IH), 4.11 (m, IH), 3.62 (m, TTT), 3.17 (m, 3H), 2.68 (m, 2H), 2.12 (m, TTT), 1.79 (m, 2H), 1.55 (m, 4H), 1.25 (m, 6H), 1.06 (t, 3H); LC/MS m/z 485 (M - HV.
Figure imgf000172_0001
4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid o- tolylamide (F-9)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid o-tolylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. Wt.: 29 mg (33%). 1H NMR (300 MHz, CDC13) δ 8.66 (d, IH), 8.45 (d, IH), 8.34 (d, IH), 8.04 (d, IH), 7.78 (d, IH), 7.71 (m, 2H), 7.60 (s, IH), 7.30 (m, 2H), 7.20 (m, 2H), 4.75 (d, IH), 4.29 (d, IH), 3.66 (d, IH), 3.31 (m, IH), 2.95 (m, IH), 2.60 (m, 1H)2.34 (s, 3H), 2.20 (m, 2H), 1.70 (m, 2H), 1.23 (m, 3H), 0.89 (t, 3H); LC/MS m/z 492 (M - H)\
Figure imgf000172_0002
4-(4-ø-Tolylcarbamoyl-naphthalene-l-sulfonyIamino)-piperidine-l-carboxyIic acid ethylamide (F-10) The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid o-tolylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and ethyl isocyanate for ethyl chloroformate. Wt.: 26 mg (47%). 1H NMR (300 MHz, CDC13) δ 8.65 (d, IH), 8.46 (d, IH), 8.32 (d, IH), 8.03 (d, IH), 7.77 (d, IH), 7.70 (m, 2H), 7.64 (s, IH), 7.30 (m, 2H), 7.20 (m, 2H), 4.81 (d, IH), 4.28 (m, IH), 3.66 (m, 2H), 3.27 (m, IH), 3.17 (m, 2H), 2.71 (m, 2H), 2.32 (s, 3H), 1.65 (m, IH), 1.25 (m, 2H), 1.07 (t, 3H); LC/MS m/z 493 (M - HV.
Figure imgf000173_0001
4-(4-ø-ToIylcarbamoyl-naphthalene-l-sulfonylamino)-piperidine-l-carboxylic acid ethyl ester (F-ll)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid o-tolylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene- 1 -carboxylic acid cyclohexylamide. Wt: 60 mg (64%). 1HNMR (300 MHz, CDC13) δ 8.67 (d, IH), 8.46 (d, IH), 8.33 (d, IH), 8.03 (d, IH), 7.79 (d, IH), 7.71 (m, 2H), 7.55 (s, IH), 7.30 (m, 2H), 7.21 (m, 2H), 4.71 (d, IH), 4.05 (q, 2H), 3.89 (m, TTT), 3.27 (m, IH), 2.72 (m, 2H), 2.31 (s, 3H), 1.65 (m, IH), 1.26 (m, TTT), 1.20 (t, 3H); LC/MS m/z 494 (M - H)\
Figure imgf000173_0002
4-(4-ø-TolyIcarbamoyI-naphthalene-l-sulfonylamino)-piperidine-l-carboxylic acid dimethylamide (F-12)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid ø-tolylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and dimethylcarbamyl chloride for ethyl chloroformate. Wt.: 35 mg (64%). !H NMR (300 MHz, CDC13) δ 8.63 (d, IH), 8.45 (d, IH), 8.33 (d, IH), 8.05 (d, IH), 7.80 (d, IH), 7.71 (m, 2H), 7.54 (s, IH), 7.30 (m, TTT), 7.20 (m, TTT), 4.68 (d, IH), 3.43 (m, 2H), 3.30 (m, IH), 2.71 (s, 6H), 2.68 (m, TTT), 2.34 (s, 3H), 1.62 (m, IH); 1.31 (m, 2H); LC/MS m/z 493 (M - H)\
Figure imgf000174_0001
4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid (2,3- dimethyl-phenyl)-amide (F-19) The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid (2,3- dimethyl-phenyl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene- 1 -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. Wt.: 64 mg (40%). 1H NMR (300 MHz, CDC13) δ 8.63 (m, 2H), 8.40 (m, IH), 8.30 (s, IH), 8.22 (d, IH), 7.72 (d, IH), 7.68 (m, IH), 7.60 (d, IH), 7.18 (m, IH), 7.10 (m, IH), 5.57 (d, IH), 4.02 (m, IH), 3.55 (m, IH), 3.28 (m, IH), 2.85 (m, IH), 2.49 (m, IH), 2.31 (s, 3H), 2.23 (s, 3H), 2.09 (2H), 1.63 (m, 2H), 1.50 (m, 2H), 1.20 (m, IH), 1.03 (m, IH), 0.84 (t, 3H); LC/MS m/z 508 (M + H)+.
Figure imgf000175_0001
4-[4-(2,3-Dimethyl-phenyIcarbamoyl)-naphthalene-l-sulfonylamino]- piperidine-1-carboxylic acid dimethylamide (F-20)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid (2,3- dimethyl-phenyl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene- 1 -carboxylic acid cyclohexylamide, and dimethycarbamyl chloride for ethyl chloroformate. Wt.: 116 mg (72%). 1H NMR (300 MHz, CDC13) δ 8.60 (m, IH), 8.40 (m, IH), 8.20 (m, 2H), 7.72 (d, IH), 7.63 (m, 2H), 7.35 (d, IH), 7.16 (m, IH), 7.09 (m, IH), 5.42 (d, IH), 3.32 (m, 2H), 3.15 (m, IH), 2.67 (s, 6H), 2.55 (m, TTT), 2.33 (s, 3H), 2.22 (s, 3H), 1.52 (m, 2H), 1.23 (m, 2H); LC/MS m/z 509 (M + H)+.
Figure imgf000175_0002
4-[4-(Tetrahydro-pyran-4-ylcarbamoyl)-naphthaIene-l-suIfonylamino]- piperidine-1-carboxylic acid dimethylamide (F-21)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid (tetrahydro- pyran-4-yl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and dimethylcarbamyl chloride for ethyl chloroformate. Wt.: 125 mg (78%). !H NMR (300 MHz, CDC13) δ 8.8.59 (m, IH), 8.29 (m, IH), 8.23 (d, IH), 7.69 (m, 2H), 7.58 (d, IH), 6.17 (d, IH), 4.82 (d, IH), 4.32 (m, IH), 4.03 (m, 2H), 3.57 (m, 2H), 3.40 (m, 2H), 3.25 (m, IH), 2.73 (s, 6TT), 2.64 (m, 2H), 2.10 (m, 2H), 1.61 (m, 4H), 1.27 (m, 2H); LC/MS m/z 489 (M + H)+.
Figure imgf000176_0001
4-(l-Butyryl-piperidin-4-ylsuIfamoyl)-naphthaIene-l-carboxylic acid (2-chloro- phenyl)-amide (F-22)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid (2-chloro- phenyl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chlroformate. Wt.: 21 mg (27%). *H NMR (300 MHz, CDC13) δ 8.67 (m, 2H), 8.48 (d, IH), 8.35 (d, IH), 8.20 (s, IH), 7.82 (d, IH), 7.72 (m, 2H), 7.41 (m, 2H), 7.09 (m, IH), 4.78 (d, IH), 4.31 (m, IH), 3.67 (m, IH), 3.35 (m, IH), 2.95 (m, IH), 2.22 (m, 2H), 1.60 (4H), 1.27 (m, 2H), 0.92 (t, 3H); LC/MS m/z 515 (M + H)+.
Figure imgf000176_0002
4-[4-(2-Chloro-phenylcarbamoyl)-naphthaIene-l-sulfonylamino]-piperidine-l- carboxylic acid dimethylamide (F-23)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid (2-chloro- phenyl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and dimethylcarbamyl chloride for ethyl chloroformate. Wt.: 28 mg (36%). 1H NMR (300 MHz, CDC13) δ 8.69 (d, IH), 8.60 (d, IH), 8.47 (d, IH), 8.35 (d, IH), 8.20 (s, IH), 7.82 (d, IH), 7.72 (m, TTT), 7.43 (m, 2H), 7.17 (m, IH), 4.83 (d, IH), 3.46 (m, 2H), 3.31 (m, IH), 2.71 (s, 6H), 2.70 (m, 2H), 1.67 (m, 2H), 1.35 (m, 2H); LC/MS m/z 516 (M + H)+.
Figure imgf000177_0001
4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthaIene-l-carboxylic acid (tetrahydro-pyran-4-yl)-amide (F-24)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene- 1 -carboxylic acid (tetrahydro- pyran-4~yl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. Wt.: 30 mg (19%). 1H NMR (300 MHz, CDC13) δ 8.67 (d, IH), 8.26 (d, IH), 8.13 (d, IH), 7.67 (m, 2H), 7.52 (d, IH), 6.68 (m, IH), 5.28 (m, IH), 4.32 (m, IH), 4.05 (m, 3H), 3.15 (m, IH), 2.46 (m, IH), 2.10 (m, 4H), 1.65 (m, 4H), 1.49 (m, 2H), 1.18 (m, IH), 9.95 (m, IH), 0.88 (t, 3H); LC/MS m/z 488 (M + H)+.
Figure imgf000177_0002
4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid phenylamide (F-25)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid phenylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. 1H NMR (300 MHz, CDC13) δ 8.87 (s, IH), 8.67 (m, IH), 8.36 (ni, 2H), 8.25 (d, IH), 8.08 (m, 2H), 7.87 (d, IH), 7.78 (d, IH), 7.70 (m, IH), 7.63 (m, IH), 5.50 (d, IH), 3.95 (m, IH), 3.55 (m, IH), 3.26 (m, IH), 2.88 (m, IH), 2.48 (m, IH), 2.13 (m, 2H), 1.66 (m, 2H), 1.48 (m, 3H), 1.19 (m, IH), 0.88 (t, 3H); LC/MS m/z 480 (M + H)+.
Figure imgf000178_0001
4-(l-Butyryl-piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid - tolylamide (F-26)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid m-tolylamide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. 'H NMR (300 MHz, CDC13) δ 8.65 (d, IH), 8.35 (d, IH), 8.27 (m, 2H), 7.70 (m, TTT), 7.60 (s, IH), 7.52 (m, IH), 7.28 (m, 2H), 7.02 (d, IH), 5.10 (d, IH), 4.07 (m, IH), 3.58 (m, IH), 3.23 (m, IH), 2.90 (m, IH), 2.50 (m, IH), 2.14 (m, 2H), 1.57 (m, 4H), 1.21 (m, IH), 1.04 (m, IH), 0.89 (t, 3H); LC/MS m/z 494 (M + H)+.
Figure imgf000178_0002
4-[4-(Cyclohexyl-methyI-carbamoyl)-naphthalene-l-sulfonylamino]-piperidine- 1-carboxylic acid ethyl ester (F-27) The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexyl- methyl-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide. 1H NMR (300 MHz, CDC13) δ 8.61 (d, IH), 8.29 (d, IH), 7.88 (m, IH), 7.65 (m, 2H), 7.42 (m, IH), 4.83 (m, IH), 4.72 (m, IH), 4.05 (q, 2H), 3.88 (m, 2H), 3.25 (m, IH), 3.05 (m, IH), 2.80 (s, 3H), 2.74 (m, IH), 1.90 (m, 4H), 1.54 (m, 8H), 1.20 (t, 3H), 0.85 (m, 2H); LC/MS m/z 502 (M + H)+.
Figure imgf000179_0001
4-[4-(CyclohexyI-methyl-carbamoyl)-naphthalene-l-suIfonylamino]-piperidine- 1-carboxylic acid dimethylamide (F-28)
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexyl- methyl-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid cyclohexylamide, and dimethylcarbamyl chloride for ethyl chloroformate. *H NMR (300 MHz, CDC13) δ 8.63 (d, TTT), 8.28 (d, IH), 7.87 (m, IH), 7.62 (m, 2H), 7.21 (m, IH), 5.35 (m, IH), 5.27 (d, IH), 4.74 (m, IH), 3.48 (m, IH), 3.35 (m, IH), 3.27 (m, IH), 3.05 (m, IH), 2.72 (s, 6H), 2.60 (s, 3H), 1.83 (m, 4H), 1.50 (m, 8H), 0.82 (m, 2H); LC/MS m/z 501 (M + H)+.
Figure imgf000179_0002
Preparation of 5-fluoro-l,2,3,4-tetrahydro-naphthalene
A modified procedure of Mirsadehgi et al. was used (J Org. Chem. 1989, 54, 3091). Boron trifluoride etherate (30.0 g, 26.8 mL, 0.21 mol) was dissolved and stirred in dimethoxyethane (50 mL) and cooled to 0°C. A solution of tetrahydro-1- naphthylamine (25 g, 0.17 mol) in dimethoxyethane (75 mL) was added dropwise and the solution was allowed to warm slowly to room temperature over the period of 1 hour. The reaction was cooled to 0°C and a solution of t-butyl nitrite (18.0 g, 20.7 mL, 0.17 mol) in dimethoxyethane (75 mL) was added dropwise. The reaction was stirred for 2 hours at 0°C upon which a large quantity of material crystallized. The solvent was removed in vacuo and chlorobenzene (200 mL) was charged to the reaction flask. The flask was stirred vigorously and heated to 135°C (Caution: N2 evolution) for 1 hour until gas evolution ceased. The flask was cooled to room temperature and the solvent removed in vacuo. Kughelrohr distillation of the residue (1 mm Hg) afforded a yellow liquid. Wt: 14.4 g (56%). *H NMR (300 MHz, CDC13) δ 7.04 (dd, IH), 6.83 (m, 2H), 2.75 (m, 4H), 1.80 (m, 4H)
Figure imgf000180_0001
Preparation of 4-fiuoro-5,6,7,8-tetrahydro-naphthalene-l-suIfonyl chloride The compound was prepared according to Scheme 10 in a similar manner to the method for preparing 4-fluoro-naphthalene-l -sulfonyl chloride. Chlorosulfonic acid (2.65 g, 1.5 mL, 22.7 mmol) was stirred in a round-bottom flask cooled by a water bath at room temperature. 5-Fluoro-l,2,3,4-tetrahydro-naphthalene (0.62 g, 4.13 mmol) was added dropwise and the dark mixture was stirred for 30 minutes until gas evolution ceased. The reaction mixture was poured carefully over a mixture of ice (75 g) and dichloromethane (100 mL) and charged to a separatory funnel. The organic layer was separated, washed with brine and dried over MgS0 . Filtration and concentration in vacuo afforded a tan solid. Wt.: 860 mg (86%). 1H NMR (300 MHz, CDC13) δ 7.97 (dd, IH), 7.02 (t, IH), 3.27 (m, 2H), 2.80 (m, 2H), 1.86 (m, ATT).
Figure imgf000181_0001
4-(4-FIuoro-5,6,7,8-tetrahydro-naphthalene-l-suIfonylamino)-piperidine-l- carboxylic acid tert-butyl ester
4-Fluoro-5,6,7,8-tetrahydro-naphthalene-l -sulfonyl chloride (860 mg, 3.46 mmol) was dissolved in THF (10 mL). Triethylamine (350 mg, 0.49 mg, 3.46 mmol) was added, followed by 4-amino-piperidine-l -carboxylic acid tert-butyl ester (694 mg, 3.46 mmol). The reaction mixture was stirred overnight at room temperature. The reaction was diluted with dichloromethane (50 mL) and charged to a separatory funnel. The organic layer was washed with water and brine, then dried over MgS0 . Filtration and concentration in vacuo afforded a yellow foam. Wt.: 1.35 g (95%). 1H NMR (300 MHz, CDC13) δ 7.88 (dd, IH), 6.95 (t, IH), 4.47 (d, TTT), 3.93 (m, 2H), 3.27 (m, IH), 3.11 (m, 2H), 2.76 (m, ATT), 1.81 (m, 6H), 1.44 (s, 9H), 1.32 (m, 2H); LC/MS m/z 411 (M - H)\
Figure imgf000181_0002
Preparation of 4-(4-Cyano-5,6,7,8-tetrahydro-naphthalene-l-suIfonylamino)- piperidine-1-carboxylic acid tert-butyl ester
4-(4-Fluoro-5,6,7,8-tetrahydro-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid tert-butyl ester (970 mg, 2.35 mmol) was dissolved in DMSO (10 mL) and sodium cyanide (577 mg, 11.77 mmol) was added. The mixture was heated overnight at 100 °C. An additional 5 equivalents of sodium cyanide (577 mg, 11.77 mmol) were added and the reaction was stirred overnight at 100 °C. The reaction was cooled to room temperature and diluted with dichloromethane (100 mL). The mixture was charged to a separatory funnel and extracted three times with water, brine and then dried over MgS0 . Filtration and concentration in vacuo afforded a brown color foam that was triturated with EtOAc to afford a tan solid. Wt.: 550 mg (56%) 'H NMR (300 MHz, CDC13) δ 7.87 (d, IH), 7.48 (d, IH), 4.52 (d, IH), 3.93 (m, 2H), 3.30 (m, IH), 3.07 (m, 4H), 2.73 (m, TTT), 1.80 (m, 6H), 1.37 (s, 9H), 1.30 (m, 2H); LC/MS m/z 418 (M - H)\
Figure imgf000182_0001
4-(4-Carbamoyl-5,6,7,8-tetrahydro-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid tert-butyl ester (F-29) and 4-(4-carboxy-5,6,7,8-tetrahydro- naphthalene-l-sulfonylamino)-piperidine-l-carboxylic acid tert-butyl ester
4-(4-Cyano-5,6,7,8-tetrahydro-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid tert-butyl ester (545 mg, 1.30 mmol) was dissolved in a mixture of isopropanol (2 ml) and 2N KOH (4 mL). The reaction was stirred for 5 days at 80 °C. The isopropanol was removed in vacuo and the residue was diluted with H20 (20 mL). The mixture was charged to a separatory funnel and extracted three times with dichloromethane. The combined organic layers were washed with brine, dried over MgS04, and concentrated in vacuo to a white solid that was triturated with dichloromethane to afford 4-(4-carbamoyl-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester F-29 as a white solid. Wt.: 340 mg (60%). 1HNMR (300 MHz, - -DMSO) δ 7.81 (m, 2H), 7.72 (d, IH), 7.52 (s, IH), 7.23 (d, IH), 3.72 (m, 2H), 3.09 (m, 3H), 2.81 (m, 2H), 2.71 (m, 2H), 1.70 (m, 4H), 1.55 (m, 2H), 1.36 (s, 9H), 1.25 (m, 2H); LC/MS m/z 436 (M - TT) . )\ The aqueous extract was acidified to pH 2 with IN HCl and extracted twice with dichloromethane. The combined organic extracts were washed with brine and dried over MgS0 . Filtration and concentration in vacuo afforded 4-(4-carboxy-5,6,7,8- tetrahydro-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester as a white solid. Wt: 76 mg (13%). 'H NMR (300 MHz, . -DMSO) δ 7.72 (d, IH), 7.33 (s, IH), 7.23 (d, IH), 3.72 (m, 2H), 3.09 (m, 3H), 2.81 (m, 2H), 2.71 (m, 2H), 1.70 (m, 4H), 1.55 (m, 2H), 1.36 (s, 9H), 1.25 (m, 2H); LC/MS m/z 437 (M - H)-.
Figure imgf000183_0001
4-[4-(3-Dimethylamino-propylcarbamoyl)-5,6,7,8-tetrahydro-naphthalene-l- sulfonylamino]-piperidine-l-carboxyIic acid tert-butyl ester (F-30) and 4-(4- Cyclohexylcarbamoyl-5,6,7,8-tetrahydro-naphthalene-l-sulfonylamino)- piperidine-1-carboxylic acid tert-butyl ester (F-31) 4-(4-Carboxy-5,6,7, 8-tetrahydro-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester (76 mg, 0.17 mmol) was dissolved in dichloromethane (2 mL). l-[3-(Dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (32 mg, 0.17 mmol) was added followed by cyclohexylamine (21 mg, 24 ml, 0.21 mmol). The reaction was stirred overnight at room temperature. The reaction was diluted with dichloromethane (15 mlO and charged to a separatory funnel. The organic layer was washed twice with water, brine and dried over MgS0 . Filtration and concentration in vacuo afforded a clear oil that was subjected to flash column chromatography (96:4 dichloromethane:methanol). Concentration of the more polar fractions afforded 4-[4-(3-dimethylamino-propylcarbamoyl)- 5,6,7,8-tetrahydro-naphthalene-l-sulfonylamino]-piperidine-l-carboxylic acid tert- butyl ester (F-30) as a yellow solid. Wt.: 40 mg, (45%). 1H NMR (300 MHz, CDC13) δ 9.05 (s, IH), 7.98 (d, IH), 7.31 (d, IH), 5.02 (d, IH), 3.96 (m, 3H), 3.37 (m, TTT), 3.20 (m, 2H), 2.83 (m, 4H), 2.70 (s, 6H), 2.13 (m, 2H), 1.97 (m, 2H), 1.83 (m, 4H), 1.42 (s, 9H), 1.32 (m, 4H); LC/MS m/z 523 (M + H)+. Concentration of the less polar fractions afforded 4-(4-cyclohexylcarbamoyl-5,6,7,8-tetrahydro- naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid tert-butyl ester (F-31) as a clear oil. Wt.: 28 mg (32%) *H NMR (300 MHz, CDC13) δ 7.87 (d, TTT), 7.20 (d, TTT), 5.73 (d, IH), 4.38 (d, IH), 3.91 (m, 3H), 3.22 (m, IH), 3.12 (m, 2H), 2.89 (m, 2H), 2.73 (m, 2H), 2.03 (m, 2H), 1.78 (m, 8H), 1.74 (m, 2H), 1.43 (s, 9H), 1.27 (m, 6H); LC/MS m/z 518 (M - HV.
Scheme 12
Figure imgf000184_0001
4-{4-[(2-Methyl-benzoylamino)-methyI]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-l)
4-(4-cyano-naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid ethyl ester (31) was prepared according to the procedure in Scheme 11, substituting for 4-(4- fluoro-naphthalene-l-sulfonylamino)-piperidine-l -carboxylic acid ethyl ester for 4- (4-fluoro-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid tert-butyl ester. To a 0 °C solution of 4-(4-cyano-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid ethyl ester (31) (615 mg, 1.59 mmol) in EtOH (10 mL) was added cobalt chloride (207 mg, 1.59 mmol). After stirring at 0 °C for 5 min under argon, sodium borohydride (181 mg, 4.77 mmol) was added into the reaction mixture. The resultant solution was stirred at 0°C for 30 minutes, and then warmed up to room temperature. After stirring for another 30 min., the resultant mixture was quenched with water. The aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by Flash column chromatography (CH2C12: MeOH) to provide 268 mg (43.0% yield) of 4-(4-aminomethyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid ethyl ester (32). LCMS showed m/z: 392 (M + H)+.
To a solution of 4-(4-aminomethyl-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid ethyl ester (32) (60 mg, 0.153 mmol) in DCE (5 mL), was added pyridine (62 ul, 0.765 mmol), 2-methyl-benzoyl chloride (22ul, 0.168 mmol) and dimethyl-pyridin-4-yl-amine (4 mg, 0.031 mmol). After stirring at 70 °C overnight, the resultant solution was concentrated in vacuo to give the crude product. Purification using reverse phase HPLC provided the title compound (G-l). LCMS showed m/z: 510 (M + H)+.
Figure imgf000185_0001
4-{4-[(2,3-Dimethyl-benzoylamino)-methyl]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-2)
The title compound was made following general procedure in scheme 10, substituting 2,3-dimethyl-benzoyl chloride for 2-methyl-benzoyl chloride. *H NMR (300 MHz, CDC13) δ 8.63 (m, IH), 8.18 (t, TTT), 7.65 (m, 2H), 7.52 (d, TTT), 7.32 (t, TTT), 7.04 (m, IH), 6.80 (m, IH), 5.10 (s, TTT), 4.00 (q, 2H), 3.80 (d, 2H), 3.20 (m, IH), 2.70 (t, 2H), 2.26 (s, 3H), 2.23 (s, 3H), 1.55 (m, TTT), 1.20 (m, TTT), 1.14 (t, 3H); LC/MS m/z 524 (M + H)+
Scheme 13
4-{4-[(4-Chloro-benzylamino)-methyl]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-7) 4-(4-Aminomethyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid ethyl ester (32) was prepared according to the procedure in Scheme 12. To a 25 °C solution of 4-(4-aminomethyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid ethyl ester (32) (62 mg, 0.159 mmol) in MeOH (4 mL) was added 4- chloro-benzaldehyde (45 mg, 0.318 mmol) and sodium cyanoborohydride (50 mg, 0.795 mmol). After stirring for 2h at 25 °C, the solution was concentrated in vacuo to give a solid. The resultant solid was purified by reverse phase HPLC providing 4- {4-[(4-chloro-benzylamino)-methyl]-naphthalene-l-sulfonylamino}-piperidine-l- carboxylic acid ethyl ester formate salt (G-7). 1H NMR (300 MHz, MeOD) δ 8.76 (m, IH), 8.38 (s, br, IH), 8.24 (d, IH), 8.18 (m, IH), 7.51 (m, 3H), 7.44 (m, 4H), 4.52 (s, 2H), 4.12 (s, 2H), 4.04 (q, 2H), 3.60 (d, 2H), 3.40 (m, IH), 2.72 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 516 (M + H)+.
Figure imgf000186_0001
4-(4-CyclohexyIaminomethyl-naphthalene-l-sulfbnylamino)-piperidine-l- carboxylic acid ethyl ester (G-8)
■ The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting cyclohexanone for 4-chloro-benzaldehyde. *H NMR (300 MHz, CDC13) δ 8.54 (d, IH), 8.25 (s, br, IH), 8.17 (s, IH), 8.04 (t, 2H), 7.70 (d, IH), 7.57 (m, TTT), 6.15 (d, IH), 4.48 (s, 2H), 4.04 (q, 2H), 3.80 (d, TTT), 3.25 (s, br, IH), 3.00 (t, IH), 2.70 (s, br, IH), 2.60 (s, IH), 2.10 (d, 2H), 1.80 (d, 2H), 1.50 (m, 5H), 1.20 (m, 7H); LC/MS m/z 475 (M + H)+
Figure imgf000186_0002
4-(4-{[(lH-ImidazoI-2-ylmethyl)-amino]-methyI}-naphthalene-l- sulfonylamino)-piperidine-l-carboxylic acid ethyl ester (G-9)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting lH-imidazole-2-carbaldehyde for 4-chloro-benzaldehyde. 'Η NMR (300 MHz, MeOD) δ 8.72 (m, IH), 8.40 (s, br, IH), 8.22 (m, 2H), 7.67 (m, 3H), 7.09 (s, TTT), 4.32 (s, 2H), 4.04 (m, 4H), 3.80 (d, 2H), 3.20 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 472 (M + H)+
Figure imgf000187_0001
4-{4-[(4-Methoxy-benzyIamino)-methyl]-naphthalene-l-sulfonylamino}- piperidine-l-carboxylic acid ethyl ester (G-10) The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 4-methoxy-benzaldehyde for 4-chloro-benzaldehyde. *H NMR (300 MHz, MeOD) δ 8.73 (d, IH), 8.22 (d, IH), 8.14 (d, IH), 7.66 (m, 3H), 7.33 (d, 2H), 6.92 (d, 2H), 4.30 (s, 2H), 4.12 (s, 2H), 4.04 (q, TTT), 3.90 (s, 2H), 3.80 (m, 5H), 3.18 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 512 (M + H)+
Figure imgf000187_0002
4-{4-[(2-Methyl-benzyIamino)-methyI]-naphthalene-l-suIfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-ll) The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 2-methyl-benzaldehyde for 4-chloro-benzaldehyde. Η NMR (300 MHz, MeOD) δ 8.76 (d, IH), 8.22 (m, 2H), 7.70 (m, 3H), 7.38 (m, IH), 7.21 (m, 3H), 4.51 (s, 2H), 4.05 (m, ATT), 3.80 (d, 2H), 3.20 (m, IH), 2.75 (m, 2H), 2.30 (s, 3H), 1.50 (m, 2H), 1.25 (m, TTT), 1.18 (t, 3H); LC/MS m/z 496 (M + H)+
Figure imgf000188_0001
4-(4-{[(Pyridin-3-ylmethyI)-amino]-methyl}-naphthalene-l-sulfonylamino)- piperidine-1-carboxylic acid ethyl ester (G-12)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting pyridine-3-carbaldehyde for 4-chloro-benzaldehyde. H NMR (300 MHz, MeOD) δ 8.72 (dd, IH), 8.57 (s, IH), 8.44 (d, IH), 8.22 (m, 2H), 7.90 (d, IH), 7.64 (m, 3H), 7.42 (dd, IH), 4.30 (s, 2H), 4.05 (q, 2H), 3.95 (s, 2H), 3.68 (d, 2H), 3.18 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, TTT), 1.18 (t, 3H); LC/MS m/z 483 (M + H)+
Figure imgf000188_0002
4-(4-{[(Furan-2-ylmethyl)-amino]-methyl}-naphthaIene-l-sulfonylamino)- piperidine-1-carboxylic acid ethyl ester (G-13)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting furan-2-carbaldehyde for 4-chloro-benzaldehyde. !H NMR (300 MHz, MeOD) δ 8.72 (dd, IH), 8.18 (m, 2H), 7.65 (m, 3H), 7.49 (m, IH), 6.39 (m, IH), 6.34 (m, IH), 4.28 (s, 2H), 4.05 (q, 2H), 3.92 (s, 2H), 3.80 (d, 2H), 3.18 (m, IH), 2.75 (m, TTT), 1.50 (m, 2H), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 472 (M + H)+
Figure imgf000189_0001
4-(4-{[(Furan-3-ylmethyl)-amino]-methyl}-naphthalene-l-sulfonylamino)- piperidine-1-carboxylic acid ethyl ester (G-14)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting furan-3-carbaldehyde for 4-chloro-benzaldehyde. !H NMR (300 MHz, MeOD) δ 8.76 (m, IH), 8.22 (m, TTT), 7.64 (m, 5H), 6.56 (m, IH), 4.42 (s, TTT), 4.05 (q, 2H), 3.95 (s, 2H), 3.80 (d, 2H), 3.20 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 472 (M + H)+
Figure imgf000189_0002
4-(4-{[(Pyridin-4-ylmethyl)-amino]-methyl}-naphthalene-l-suIfonylamino)- piperidine-l-carboxylic acid ethyl ester (G-15)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting pyridine-4-carbaldehyde for 4-chloro-benzaldehyde. *H NMR (300 MHz, MeOD) δ 8.70 (m, IH), 8.54 (s, IH), 8.24 (m, 4H), 7.68 (m, 2H), 7.45 (m, IH), 7.14 (m, IH), 4.70 (m, 2H), 4.55 (m, 2H), 4.05 (q, 2H), 3.80 (d, 2H), 3.18 (m, IH), 2.75 (m, 2H), 1.50 (m, TTT), 1.25 (m, 2H), 1.18 (t, 3H); LC/MS m/z 483 (M + H)+
Figure imgf000189_0003
4-{4-[(3-Chloro-benzylamino)-methyl]-naphthaIene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-16)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 3-chloro-benzaldehyde for 4-chloro-benzaldehyde. !H NMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.20 (m, 2H), 7.66 (m, 3H), 7.45 (s, IH), 7.30 (m, 3H), 4.25 (s, 2H), 4.05 (q, 2H), 3.90 (s, 2H), 3.78 (d, 2H), 3.20 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.17 (t, 3H); LC/MS m/z 516 (M + H)+
Figure imgf000190_0001
4-{4-[(4-Fluoro-benzylamino)-methyl]-naphthaIene-l-sulfonyIamino}- piperidine-1-carboxylic acid ethyl ester (G-17)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 4-fluoro-benzaldehyde for 4-chloro-benzaldehyde. "H NMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.19 (m, 2H), 7.66 (m, 3H), 7.40 (m, 2H), 7.06 (m, 2H), 4.25 (s, 2H), 4.05 (q, 2H), 3.85 (s, 2H), 3.78 (d, 2H), 3.18 (m, IH), 2.75 (m, TTT), 1.50 (m, 2H), 1.25 (m, TTT), 1.17 (t, 3H); LC/MS m/z 500 (M + H)+
Figure imgf000190_0002
4-(4-{[(Pyridin-2-ylmethyl)-amino]-methyl}-naphthalene-l-sulfonyIamino)- piperidine-1-carboxylic acid ethyl ester (G-18)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting pyridine-2-carbaldehyde for 4-chloro-benzaldehyde. 1H NMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.52 (m, IH), 8.24 (m, 2H), 7.80 (t, IH), 7.67 (m, 3H), 7.52 (d, IH), 7.30 (t, IH), 4.30 (s, 2H), 4.00 (m, 4H), 3.80 (d, TTT), 3.18 (m, IH), 2.75 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.17 (t, 3H); LC/MS m/z 483 (M + H)+
Figure imgf000191_0001
4-{4-[(Cyclohexyl-ethyl-amino)-methyl]-naphthaIene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-20)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting acetaldehyde for 4-chloro-benzaldehyde, and substituting 4-(4-cyclohexylammomethyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 -carboxylic acid ethyl ester (G-8) for 4-(4-aminomethyl-naphthalene-l-sulfonylamino)- piperidine-1 -carboxylic acid ethyl ester. 1H NMR (300 MHz, MeOD) δ 8.79 (m, IH), 8.36 (m, 2H), 8.27 (dd, IH), 7.77 (m, 3H), 4.62 (s, 2H), 4.05 (q, 2H), 3.80 (d, 2H), 3.25 (m, IH), 3.05 (m, 3H), 2.75 (m, 2H), 2.10 (d, 2H), 1.80 (d, 2H), 1.65 (m, 3H), 1.48 (m, 2H), 1.22 (m, 1 IH); LC/MS m/z 502 (M + H)+
Figure imgf000191_0002
4-{4-[(2-Chloro-benzylamino)-methyI]-naphthalene-l-suIfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-21) The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 2-chloro-benzaldehyde for 4-chloro-benzaldehyde. 'H NMR (300 MHz, MeOD) δ 8.72 (d, IH), 8.15 (d, 2H), 7.66 (m, 3H), 7.52 (m, IH), 7.38 (m, IH), 7.28 (m, 2H), 4.30 (s, TTT), 4.00 (m, ATT), 3.78 (d, 2H), 3.18 (m, IH), 2.72 (m, 2H), 1.50 (m, 2H), 1.25 (m, 2H), 1.17 (t, 3H); LC/MS m/z 516 (M + H)+
Figure imgf000192_0001
4-{4-[(3-Phenyl-propylamino)-methyl]-naphthalene-l-sulfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-23)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting 3-phenyl-propionaldehyde for 4-chloro-benzaldehyde. *H NMR (300 MHz, MeOD) δ 8.74 (m, IH), 8.25 (m, IH), 8.20 (d, IH), 7.70 (m, 2H), 7.59 (m, IH), 7.19 (m, 5H), 4.33 (s, 2H), 4.05 (q, 2H), 3.78 (d, TTT), 3.18 (m, IH), 2.73 (m, 6H), 1.90 (m, 2H), 1.48 (m, 2H), 1.23 (m, 2H), 1.17 (t, 3H); LC/MS m/z 510 (M + H)+
Figure imgf000192_0002
4-[4-(Phenethylamino-methyl)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (G-24)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting phenyl-acetaldehyde for 4-chloro-benzaldehyde. Η
NMR (300 MHz, MeOD) δ 8.74 (m, IH), 8.19 (m, TTT), 1.61 (m, 2H), 7.59 (m, IH), 7.22 (m, 5H), 4.35 (s, 2H), 4.05 (q, 2H), 3.78 (d, 2H), 3.18 (m, IH), 2.92 (m, ATT), 2.62 (m, 2H), 1.90 (m, 2H), 1.48 (m, 2H), 1.25 (m, 2H), 1.17 (t, 3H); LC/MS m/z A96 (M + TT
Figure imgf000192_0003
4-{4-[(l-Methyl-piperidin-4-ylamino)-methyl]-naphthalene-l-sulfonylamino}- piperidine-l-carboxylic acid ethyl ester (G-25)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting l-methyl-piperidin-4-one for 4-chloro-benzaldehyde. 1H NMR (300 MHz, CDC13) δ 8.73 (m, IH), 8.45 (s, IH), 8.28 (m, IH), 8.22 (d, IH), 7.70 (m, 3H), 4.40 (s, TTT), 4.05 (q, 2H), 3.80 (d, 2H), 3.45 (d, 2H), 3.20 (m, IH), 3.00 (m, 3H), 2.78 (s, 3H), 2.72 (m, 2H), 2.25 (d, 2H), 1.80 (m, 2H), 1.50 (d, 2H), 1.25 (m, 2H), 1.17 (t, 3H); LC/MS m/z 487 (M + H)+
Figure imgf000193_0001
4-{4-[(Cyclohexylmethyl-amino)-methyl]-naphthaIene-l-suIfonylamino}- piperidine-1-carboxylic acid ethyl ester (G-27)
The title compound was prepared as its formate salt following the general procedure in Scheme 13, substituting cyclohexanecarbaldehyde for 4-chloro-benzaldehyde. *H NMR (300 MHz, MeOD) δ 8.76 (m, IH), 8.52 (s, IH), 8.26 (m, 2H), 7.72 (m, 3H),
4.49 (s, TTT), 4.05 (q, 2H), 3.80 (d, 2H), 3.20 (m, IH), 2.75 (m, 4H), 1.75 (m, 6H),
1.50 (d, 2H), 1.25 (m, 5H), 1.18 (t, 3H), 1.00 (m, 2H); LC/MS m/z 488 (M + H)+
Scheme 14
Figure imgf000194_0001
EtOCOCI *- P-carbonate
Figure imgf000194_0003
Figure imgf000194_0002
37 38
Figure imgf000194_0004
39 G-30
Figure imgf000194_0005
4-[4-(l-CycIohexylamino-ethyl)-naphthalene-l-sulfonyIamino]-piperidine-l- carboxylic acid ethyl ester (G-30)
4-Cyano-naphthalene-l -sulfonic acid (l-benzyl-piperidin-4-yl)-amide (33) was prepared according to the general procedure in Scheme 11, substituting 1-benzyl- piperidin-4-ylamine for 4-amino-piperidine-l -carboxylic acid tert-butyl ester. To a solution of 4-cyano-naphthalene-l -sulfonic acid (l-benzyl-piperidin-4-yι)-amide 33 (3.0 g, 7.43 mmol) in H20 (70 mL) was added KOH (4.2 g, 75 mmol). After stirring at 100 °C overnight, the resultant mixture became a clear solution. The aqueous layer was washed with CH2C12 twice and acidified to pH 4 by adding hydrochloric acid. After filtration, the resultant solid was dried to give 1.8 g of crude 4-(l- benzyl-piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid 34 in 57% yield. LCMS showed m/z: 425 (M + H)+. This material was used without further purification.
To a solution of 4-(l-benzyl-piperidin-4-ylsulfamoyl)-naphthalene-l-carboxylic acid 34 (212 mg, 0.5 mmol) in DCE (5 mL), was added O,N-dimethyl-hydroxylamine hydrochloride (59 ul, 0.6 mmol), PS-carbodiimide (1.9g, 2.5 mmol), triethyl amine (140 uL, 1 mmol) and HOAt (102 mg, 0.75 mmol). After stirring at 50 °C overnight, the resultant solution was filtered and concentrated in vacuo to give the crude product 4-(l-benzyl-piperidin-4-ylsulfamoyl)-naphthalene-l -carboxylic acid methoxy-methyl-amide 35. LCMS showed m/z: 468 (M + H)+. This material was used without further purification.
To a 0 °C solution of 4-( 1 -benzyl-piperidin-4-ylsulfamoyl)-naphthalene- 1 - carboxylic acid methoxy-methyl-amide 35 (200 mg, 0.43 mmol) in THF (5 mL) was slowly added methylmagnesium bromide (5.71 mL, 17.1 mmol, IM THF solution). After stirring at 25 °C for 4h, the resultant mixture was quenched with saturated ammonium chloride solution. The aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS0 . The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by Flash column chromatography (hexane/EtOAc) to provide 118 mg of 4-acetyl-naphthalene-l -sulfonic acid (l-benzyl-piperidin-4-yι)-amide 36 in 56% overall yield (for two steps).LCMS showed m/z : 423 (M + H)+.
Following the general procedure in Scheme 4-2, deprotection of 4-acetyl- naphthalene-l -sulfonic acid (l-benzyl-piperidin-4-yl)-amide 36 occurred concomitant with reduction of the ketone group to afford 4-(l-hydroxy-ethyl)- naphthalene-1 -sulfonic acid piperidin-4-ylamide acetic acid salt 37 as product. LCMS showed m/z: 334 (M + H)+. This material was used without further purification. To a solution of 4-(l-hydroxy-ethyl)-naphthalene-l-sulfonic acid piperidin-4- ylamide acetic acid salt 37 (290 mg, 0.74 mmol) in MeOH (10 mL) was added MP- Carbonate (1.45 g, 3.69 mmol, 2.54 mmol/g). After shaking at 25 °C for lh, the solution was filtered. To the resultant solution was added ethyl chloroformate (120 mg, 1.11 mmol). After stirred for another 2h at 25 °C, the solution was concentrated in vacuo to give a solid. The crude material was purified by Flash column chromatography (CH2C12: MeOH) to provide 4-[4-(l-hydroxy-ethyl)-naphthalene-l- sulfonylamino] -piperidine- 1 -carboxylic acid ethyl ester 38. LCMS showed m/z : 407 (M + H)+.
To a -78 °C solution of oxalyl dichloride (85 mg, 0.665 mmol) in CH2C12 (10 mL) was added DMSO (104 mg, 1.33 mmol). After stirred at -78 °C for 10 min, a solution of 4-[4-(l-hydroxy-ethyl)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester 38 (180 mg, 0.443 mmol) in CH2C12 was added into the mixture by dropwise. The resultant mixture was stirred at -78 °C for another 30 min, then was added triethyl amine (224 mg, 2.22 mmol). The reaction mixture was warmed up to room temperature and stirred for 2h. The resultant mixture was quenched with saturated ammonium chloride solution and the aqueous layer was extracted with CH2C12. The organic extracts were combined, washed with brine and dried over MgS04. The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by Flash column chromatography (CH2C12: MeOH) to provide 45 mg of 4-(4-acetyl-naphthalene-l-sulfonylamino)- piperidine-1 -carboxylic acid ethyl ester 39 in 25% yield. LCMS showed m/z : 409 (M + H)+.
To a 25 °C solution of 4-(4-acetyl-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid ethyl ester 39 (45 mg, 0.11 mmol) in MeOH (4 mL) was added cyclohexylamine (31 mg, 0.22 mmol) and sodium cyanoborohydride (34 mg, 0.69 mmol). After stirring for 2h at 25 °C, the solution was concentrated in vacuo to give a solid. The resultant solid was purified by reverse phase HPLC providing the title compound (G-30). 1H NMR (300 MHz, MeOD) δ 8.84 (m, IH), 8.42 (s, br, IH), 8.35 (m, 2H), 7.82 (m, 3H), 5.55 (d, IH), 4.02 (q, 2H), 3.80 (d, 2H), 3.22(m, IH), 3.00 (m, IH), 2.77(s, br, 2H), 2.19 (d, IH), 2.05 (d, IH), 1.78 (m, 4H), 1.50 (m, 5H), 1.24 (m, 9H); LC/MS m/z 488 (M + H)+.
Scheme 15
Figure imgf000197_0001
4-Methyl-naphthalene-l-sulfonic acid cyclohexylamide (40)
To a solution of 4-methyl-naphthalene -1-sulfonyl chloride (2.4 g, 10.0 mmol) in CH2C12 (30 mL), was added cyclohexylamine (1.4 g, 11.0 mmol) and triethylamine (2.8 mL, 20.0 mmol) and the resultant solution was stirred at room temperature overnight. The solution was quenched with water and extracted with CH2C12 (3x30 mL). The combined organic layers were dried over Na2S0 and concentrated in vacuo. The resulting residue was purified by Flash column chromatography (hexane/ethyl acetate, gradient elution) to give the title compound 40 (2.0 g) as a yellow solid. ^NMR (300 MHz, CDC13) δ 8.63 (d, IH), 8.18 (d, IH), 8.10 (d, IH), 7.64 (m, 2H), 7.38 (d, IH), 3.08 (m, IH), 2.76 (s, 3H), 1.52 (m, 5H), 1.09 (m, 5H); LC/MS m/z 304 (M + H)+.
Figure imgf000198_0001
4-Bromomethyl-naphthalene-l-sulfonic acid cyclohexylamide (41)
To a solution of 4-methyl-naphthalene-l -sulfonic acid cyclohexylamide 40 (3.0 g, 10 mmol) in CC14 (100 mL) was added NBS (2.1 g, 12.0 mmol) and benzoyl peroxide (240 mg, 1.0 mmol), The reaction mixture was heated at reflux overnight. The solid was filtered and the filtrate was concentrated in vacuo. The title compound was a yellow residue (2.5 g, solidified on standing) which was used directly in the next step without further purification. !H NMR (300 MHz, CDC13) δ 8.70 (m, IH), 8.25 (m, 2H), 7.70 (m, 2H), 7.60 (d, IH), 4.94 (s, 2H), 4.58 (m, IH); 3.15 (m, IH), 1.55 (m, 5H), 1.05 (m, 5H); LC/MS m/z 356 (M + H)+ 382.
Figure imgf000198_0002
4-(l,3-Dioxo-l,3-dihydro-isoindol-2-ylmethyl)-naphthalene-l-suIfonic acid cyclohexylamide (G-4) To a solution of 4-bromomethyl-naphthalene-l -sulfonic acid cyclohexylamide 41 (150 mg, 0.39 mmol) in DMF (5 mL) was added potassium phthalimide (109 mg, 0.58 mmol). The resultant solution was stirred at room temperature and then heated to 100°C for 3 hr. The reaction was quenched with water and extracted with CH2C12. The organic layers were dried and concentrated in vacuo. HPLC purification of the residue gave the title compound (G-4) (63 mg) as white foam. *H NMR (300 MHz, MeOD) δ 8.67 (d, IH), 8.42 (d, IH), 8.22 (d, IH), 7.88 (m, 23H), 7.76 (m, 4H), 5.48 (s, 2H), 4.48 (d, IH), 3.12 (d, IH), 1.58 (m, 6H), 1.10 (m, ATT); LC/MS m/z 449 (M + H)+.
Figure imgf000198_0003
4-Aminomethyl-naphthalene-l-sulfonic acid cyclohexylamide (42) To a solution of 4-(l,3-dioxo-l,3-dihydro-isoindol-2-ylmethyl)^naphthalene-l- sulfonic acid cyclohexylamide (G-4) (1.6 g, 3.57 mmol) in methanol (30 mL) was added hydrazine (2 mL). The resultant solution was stirred at room temperature overnight. A precipitate was formed and filtered. The solid was further washed with small amount of methanol. The filtrate was collected and solvent was removed in vacuo. Flash chromatography of the residue with Flash column (MeOH/CH2Cl2: 5-10%) gave the title compound (42) as white solid (0.7 g). 1H NMR (300 MHz, DMSO) δ 8.68 (d, IH), 8.24 (d, IH), 8.13 (d, IH), 7.60 (m, 3H), 5.00 (s, IH), 4.39 (s, 2H), 3.10 (s, IH), 2.03 (m, 2H), 1.59 (m, 4H), 1.08 (m, 4H); LC/MS m/z 319 (M + H)+.
Figure imgf000199_0001
N-(4-CyclohexylsuIfamoyl-naphthalen-l-yImethyl)-2-methyl-benzamide (G-5) To a solution of naphthalenyl methylamine 42 (100 mg, 0.32 mmol) in DMF (2 mL) was added o-tolylchloride (49 DL, 0.38 mmol) and triethylamine (88 DL, 0.63 mmol). The resultant solution was stirred at room temperature overnight. The solvent was removed in vacuo and the residue was purified using HPLC to give the title compound (G-5) (30 mg) as pale yellow solid. 1H ΝMR (300 MHz, MeOD) δ 8.78 (d, IH), 8.34 (d, IH), 8.20 (d, IH), 7.72 (m, 2H), 7.63 (d, IH), 7.35 (d, IH), 7.30 (d, IH), 7.20 (d, IH), 5.07 (s, 2H), 2.95 (s, IH), 2.34 (s, 3H), 1.55 (m, 5H), 1.05 (m, 5H),; LC/MS m/z 437 (M + H)+.
Figure imgf000199_0002
Furan-2-carboxyIic acid (4-cyclohexyIsuIfamoyl-naphthalen-l-yImethyl)-amide (G-6) The title compound was made following general procedure in Scheme 15, substituting furan-2-carboxylic chloride for o-tolyl chloride. 1H NMR (300 MHz, MeOD) δ 8.76 (d, IH), 8.26 (d, IH), 8.18 (d, IH), 7.67 (d, IH), 7.50 (d, IH), 7.16 (d, IH), 6.58 (m, IH), 5.08 (s, 2H), 2.87 (s, IH), 1.52 (m, 5H), 1.11 (m, 5H),; LC/MS m/z 413 (M + H)+.
Figure imgf000200_0001
4-Cyclohexylaminomethyl-naphthaIene-l-sulfonic acid cyclohexylamide (G-31)
The title compound was prepared according to the general procedure in Scheme 15, substituting cyclohexylamine and potassium carbonate for potassium phthalimide.
HPLC purification of the residue gave the title compound (77 mg) as white foam.
1H NMR (300 MHz, MeOD) δ 8.80 (m, IH), 8.37 (s, IH), 8.26 (d, 2H), 7.78 (m,
3H), 4.79 (s, TTT), 3.36 (m, IH), 2.96 (m, IH), 2.30 (m, 2H), 1.90 (m, 2H), 1.72 (m,
IH), 1.48 (m, 10H), 1.10 (m, 2H); LC/MS m/z 401(M + H)+.
Figure imgf000200_0002
4-[4-(Benzylamino-methyl)-naphthalene-l-sulfonylamino]-piperidine-l- carboxylic acid ethyl ester (G-32)
The intermediate 4-(4-methyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester was prepared according to the general procedure in Scheme 15, substituting 4-amino-piperidine-l -carboxylic acid tert-butyl ester for cyclohexylamine.
The intermediate 4-(4-bromomethyl-naphthalene- 1 -sulfonylamino)-piperidine- 1 - carboxylic acid tert-butyl ester was prepared according to the general procedure in Scheme 15 substituting 4-(4-methyl-naphthalene-l-sulfonylamino)-piperidine-l- carboxylic acid tert-butyl ester for 4-methyl-naphthalene-l -sulfonic acid cyclohexylamide (40).
The title compound was prepared according to the general procedure in Scheme 15, substituting phenylamine and potassium carbonate for potassium phthalimide. HPLC purification gave the title compound (15 mg) as a white solid. 'H NMR (300 MHz, MeOD) δ 8.73 (d, IH), 8.29 (s, IH), 8.22 (m, IH), 8.04 (m, IH), 7.68 (m, 3H), 7.20 (m, 2H), 4.59 (s, 2H), 4.23 (s, 2H), 3.97 (AB q, 2H), 3.67 (m, 2H), 3.16 (m, 1H),2.70 (m, 2H), 1.44 (m, 2H), 1.22 (m, 2H), 1.13 (t, 3H); LC/MS m/z 482 (M + H)+.
The Sulfonamides Inhibit CCR8:
This whole cell binding screen evaluates the ability of compounds to inhibit biotinlyated human 1309 binding to the cloned human CCR8 receptor stably expressed in LI .2 cells. Human CCR8 gene was amplified by PCR using PFU polymerase under standard conditions from human genomic DNA purchased from Stratagene. The PCR primers used were: 5' CCR8 5'tttggatccatggattatacacttgacctcagtgtg3' (SEQ ID NO: 1)
3' CCR8
5'tttgcggccgctcacaaaatgtagtctacgctggagg3' (SEQ ID NO: 2)
The 5' and 3' primers contained flanking enzyme sites (Bam Hi and Not 1, respectively), which were used to subclone the gene into pcDNA3.1. The vector containing the CCR8 gene was sequenced by manual sequencing and matched to the reported hCCR8 sequence. The CCR8 vector was then transfected into LI.2 cells (murine pre-B cells) by electroporation. Positive clones were selected by functional chemotaxis and binding to the ligand 1309. Compounds were screened using the FMAT™ 8100 HTS System (purchased from Applied Biosystems).
A suspension was prepared of L1.2/hCCR8 cells at 4.0 x 105 cells/mL in a binding buffer (Buffer consisting of Hanks Balanced Salt Solution (without phenol red), 1 OmM HEPES, 0.1% Fatty Acid Free BSA, 0.02% Sodium Azide). A solution of 0.375 nM of Human 1-309 (Biotinylated at the C-terminus of the ligand after an additional lysine residue using the Applied Biosystems 433 peptide synthesizer) and 0.375 nM of mouse Cy-5 Mab-D-Biotin (Jackson ImmunoResearch Laboratories, Inc., Code Number 200-172-096) was prepared in binding buffer immediately prior to the assay.
Dilution series of 10 mM stock concentrations of the test compounds were prepared in DMSO and further diluted into binding buffer defined above) to three times the final assay concentration.
10 point concentration response curve is constructed for each compound, starting at 10 μM (final assay concentration in Binding Buffer). 25 μl of each concentration of test were transferred into the appropriate wells of a 384 plate. 25 μl of cold 100 nM 1-309 (R and D Systems: Catalog Number 272-I/CF) were then transferred into empty wells to serve as a control for non-specific binding. 25 μl of the 0.375nM Biotinylated Human 1-309/ 0.375nM Cy5-D-Biotin solution were then transferred into each well of the same 384 well plate, followed by addition of 25 μl of the resuspended cell solution into each well. The components were mixed in wells by covering the plate with aluminum foil and rotating for 0.5 hours. The plates was allowed to incubate at room temperature for approximately 1-2 hours and then read on FMAT™ 8100 HTS System (PMT= 490/518 or 537/568, Set threshold = 1SD MAT). Average fluorescence reported for each concentration was normalized to percent inhibition based on negative (no inhibitor) and positive (100 nM excess unlabeled 1309 (R and D Systems) controls. Table 1: Ki of compounds to inhibit 1-309 binding to CCR8 (uM)
Figure imgf000203_0001
Figure imgf000204_0001
Figure imgf000205_0001
Figure imgf000206_0001
Figure imgf000207_0001
Figure imgf000208_0001
Figure imgf000209_0001
Figure imgf000210_0001
Figure imgf000211_0001
Figure imgf000212_0001
Figure imgf000213_0001
While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.

Claims

What is claimed is:
A compound represented by the following structural formula:
Figure imgf000215_0001
or a pharmaceutically acceptable salt thereof, wherein: Xi is a covalent bond, C=0 or CRaRb> X is a covalent bond, O, or NR5; C=Z is C=0, CH2, C=NH, C=S or absent, provided that when Xi is a covalent bond then C=Z is not CH2, provided that when C=Z is absent then X is a covalent bond, and provided that when X is NR5 and C=Z is C=0 then R4 is not an aliphatic or substituted aliphatic group;
Ra and Rb are independently H or a C1-C3 alkyl; R1 is: i) a substituted or unsubstituted aromatic group; ii) a substituted or unsubstituted non-aromatic ring; or iii) when X is NR5, then NR5-(CH2)mR1, taken together, is optionally a substituted or unsubstituted non-aromatic heterocyclic group;
R2 is -H or a C1-C3 alkyl group; R3 is -H; and R4 is: i) a substituted or unsubstituted aliphatic group; ii) a substituted or unsubstituted aromatic group; iii) a substituted or unsubstituted non-aromatic ring or a substituted or unsubstituted non-aromatic bridged bicyclic group; or iv) R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group;
R5 is -H, or a C1-C3 alkyl group;
Ring B is phenyl group or five or six membered carbocyclic non-aromatic ring fused to Ring A; Rings A and B are optionally substituted with alkyl, halolkyl, alkoxy, haloalkoxy, hydroxy, halogen, cyano or nitro; m is 0, 1, 2 or 3; n is 1 or 2; each substitutable carbon atom of the aromatic group represented by R1 is optionally substituted with a group represented by R10, wherein R10 is halogen, -
R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -O(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -NO2, -CN, -N(R')2, -NR'C02R°, -NR'C(0)R°, -NR'NR'C(0)R°, -N(R')C(O)N(R')2, -NR'NR'C(O)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(O)CH2C(0)R°, -C02R°,
-C(O)R°, -C(O)N(R0)2, -OC(0)R°, -OC(O)N(R°)2, -S(O)2R°, -S02N(R')2, - S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R°, -V-OH, -V-OR0, -V-SH, -V-SR0, -V-N02> - V-CN, -V-N(R')2, -V-NR'C02R°, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°,
-V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-C02R°, -V-C(0)R°, -V-C(0)N(R°)2, -V-OC(0)R°, -V-OC(0)N(R°)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, - V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, or -V-C(=NH)-N(R') , and each group represented by R10 is independently selected; each substitutable carbon atom of the aliphatic group represented by R4 is optionally substituted with a group represented by R11, wherein R11 is halogen, - R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -O(Ph), substituted -0(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -NO2, -CN, -N(R')2, -NR'C02R°, -NR'C(O)R0, -NR'NR'C(0)R0^ -N(R')C(0)N(R')2,
-NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C(0)R°, -C(O)N(R°)2, -OC(O)R°, -OC(0)N(R°)2, -S(O)2R°, -SO2N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R0, -V-OH, -V-OR0, -V-SH, -V-SR0, -V-N02, -V-CN, -V-N(R')2, -V-NR'C02R°, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'CO2R°,
-V-C(O)C(O)R0, -V-C(0)CH2C(0)R°, -V-C(0)R°, -V-C(0)N(R°)2, -V-OC(0)R°, -V-OC(0)N(R°)2, -V-S(O)2R°, -V-S02N(R')2, -V-S(O)R°, -V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, -V-C(=NH)-N(R')2, =NNHR*, =NN(R*)2, =NNHC(0)R*, =NNHC02(alkyl), =NNHS02 (alkyl), or =NR*, and each group represented by R1 * is independently selected; each substitutable carbon atom of the aromatic group represented by R4 is optionally substituted with a group represented by R12, wherein R12 is halogen, - R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -O(Ph), substituted -0(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -CN, -NR'C02R°,
-NR'NR'C(0)R°, -N(R')C(0)N(R')2, -NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(0)R°, -OC(0)R°, -OC(0)N(R°)2, -S(0)2R°, -S02N(R')2, -S(O)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R0, -V-OH, -V-OR0, -V-SH, -V-SR0, -V-CN, -V-NR'C02R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2,
N-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°, -V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-C02R°, -V-C(0)R°, -V-OC(O)R°, -V-OC(0)N(R°)2, -V-S(O)2R0, -V-S02N(R')2, -V-S(0)R°, -V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2 or -V-C(=NH)-N(R')2, and each group represented by R12 is independently selected; each substitutable carbon atom of: i) the non-aromatic ring represented by R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR*; iii) the nitrogen-containing non-aromatic heterocyclic group formed from NR3R4; and iv) the non-aromatic bridged bicyclic group represented by R4 is optionally and independently substituted with -R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2- methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -0(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -CN, -N02, -N(R')2, -C(O)N(R°)2, -NR'C(0)R°, -NR'C(0)R°, -V-N(R')2, -V-NR'C(0)R°, -V-C(O)N(R°)2, -NR'CO2R°, -NR'NR'C(O)R°, -N(R')C(0)N(R')2, -NR'NR'C(O)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(O)R°, -OC(0)R°, -OC(0)N(R°)2, -S(O)2R0,
-S02N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R°, -V-OH, -V-OR0, -V-SH, -V-SR0, -NR'C(0)R°, -V-N02, -V-CN, -V-N(R')2, -V-NR'C02R°, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R0, -V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-C02R°, -V-C(O)R°,
-V-C(0)N(R°)2, -V-OC(O)R°, -V-OC(O)N(R0)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, -V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, -V-C(=NH)-N(R')2, =0, =S, =NNHR*, =NN(R*)2, =NNHC(0)R*, =NNHC02(alkyl), =NNHS02 (alkyl) or =NR* ; each R° is independently hydrogen or substituted or unsubstituted aliphatic group, a substituted or unsubstituted cycloaliphatic, a substituted or unsubstituted non-aromatic heterocyclic group or a substituted or unsubstituted aromatic group selected from phenyl, naphthyl, 2-furanyl, 3-furanyl, N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2- oxadiazolyl, 5-oxadiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 1-pyrrolyl, 2- pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5- pyrimidyl, 3-pyridazinyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-triazolyl, 5- triazolyl, tetrazolyl, 2-thienyl, 3 -thienyl, carbazolyl, benzimidazolyl, benzothienyl, benzofuranyl, indolyl, quinolinyl, benzotriazolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoquinolinyl, indolyl, isoindolyl, acridinyl, or benzoisazolyl; each R' is independently R°, -C02R°, -S02R° or -C(0)R°; each R* is independently hydrogen, an unsubstituted aliphatic group or a substituted aliphatic group;
V is a C1-C6 alkylene group; each substitutable carbon atom of : i) the aliphatic, cycloaliphatic, non- aromatic heterocyclic group and aromatic group represented by R°; and ii) the aliphatic group represented by R* is optionally and independently substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, aminoalkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl; each substitutable nitrogen atom of: i) the non-aromatic ring represented by R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR1; iii) the nitrogen-containing non-aromatic heterocyclic group formed from NR3R4; iv) the non-aromatic heterocyclic group represented by Ro; and v) the non- aromatic bridged bicyclic group represented by R4 is optionally and independently substituted with R+, -N(R+)2, -C(0)R+, -C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N(R+)2, -C(=S)N(R+)2, -C(=NH)-N(R+)2, -NR+ S02 R+, -C(0)-NHR+, -C(0)-N(R+)2, -C(0)-CH[N(R+)2]R+ or -C(0)-CH[OR+]R+; each R+ is independently hydrogen, an unsubstituted heteroaryl or an aliphatic, cycloaliphatic, non-aromatic heterocyclic group, phenyl or benzyl group, wherein each substitutable carbon atom of the aliphatic, cycloaliphatic, non- aromatic heterocyclic ring, phenyl or benzyl group represented by R+ is optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl or N(R+)2 is a non-aromatic heterocyclic group; and each substitutable nitrogen atom of the non-aromatic heterocyclic group represented by R+ is optionally substituted with alkyl, alkoxycarbonyl, alkylcarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl, provided that the compound is other than N-[4-[[(4- methoxyphenyl)amino]sulfonyl]-l-naphthalenyl]-benzamide, N-[4-[(2- propenylamino)sulfonyl]-l-naphthalenyl]-benzamide, N-[4-(4- morpholinylsulfonyl)-l-naphthalenyl]-benzamide or N-[4-(l-piperidinylsulfonyl)- 1 -naphthalenyl]-benzamide. The compound of Claim 1 wherein the compound is represented by the following structural formula:
Figure imgf000220_0001
wherein:
C=Z is C=0, CH2,C=NH or C=S;
Rings A and B are optionally substituted with alkyl, halolkyl, alkoxy, haloalkoxy, hydroxy, halogen, cyano or nitro;
R4 is a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group or a substituted or unsubstituted non-aromatic ring; each substitutable nitrogen atom of: i) the non-aromatic ring represented by R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR1; iii) the nitrogen-containing non-aromatic heterocyclic group formed from R3, R4 and the nitrogen atom to which R3 and R4 are bonded; and iv) the non-aromatic heterocyclic group represented by R° are selected from R+, -N(R+)2, -C(0)R+, - C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N(R )2, -C(=S)N(R+)2, -C(=NH)-N(R+)2 and -NR+ S02 R+; and each R+ is independently hydrogen, an unsubstituted heteroaryl or an unsubstituted non-aromatic heterocyclic ring or an aliphatic, phenyl or benzyl group optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
The compound of Claim 2 wherein: C=Z is C=0 and Xi is a bond;
X is a bond;
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more groups R10; R2 is -H;
R3 is -H or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group;
R4 is a substituted or unsubstituted non-aromatic ring or a phenyl or benzyl group optionally substituted with one or more groups R12; m is 0 or 1; or n is 2.
4. The compound of Claim 2 wherein: C=Z is C=0 and Xi is a bond;
X is a bond;
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more groups R10; R2 is -H; R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is O or 1; and n is 2.
5. The compound of Claim 4 wherein the compound is represented by the following structural formula:
Figure imgf000222_0001
wherein Rings A and B are unsubstituted
6. The compound of Claim 1 wherein the compound is represented by the following structural formula:
Figure imgf000222_0002
wherein:
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1;
Rings A and B are unsubstituted; each substitutable nitrogen atom in: i) a nitrogen-containing the non- aromatic heterocyclic group formed from -NR3R4; and ii) the non-aromatic ring represented by R4 are R+, -N(R+)2, -C(0)R+, -CO2 R+, -C(O)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N(R+)2, -C(=S)N(R+)2, -C(=NH)-N(R+)2 and -NR+S02R+; and each R+ is independently hydrogen, an unsubstituted heteroaryl or an unsubstituted non-aromatic heterocyclic ring or an aliphatic, phenyl or benzyl group optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
The compound of Claim 1 wherein the compound is represented by the following structural formula:
Figure imgf000223_0001
wherein:
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1; and Rings A and B are unsubstituted.
8. The compound of Claim 5 wherein R4 is a substituted or unsubstituted non- aromatic ring.
The compound of Claim 8 wherein R4 is a piperidinyl group or an N-substituted piperidinyl group.
10. The compound of Claim 1 wherein the compound is represented by the following structural formula:
Figure imgf000224_0001
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H;
R4 is a piperidinyl group N-substituted with R15, -C(0)R15, -C(0)OR15, -C(0)-ΝHR15, -C(O)-N(R15)2,or -C(0)CH[N(R16)2]R17; each substitutable carbon of the piperidinyl group represented by R4 is optionally and independently substituted with an aliphatic group or substituted aliphatic group;
R15 is -H, a substituted or unsubstituted ion-aromatic ring, or a substituted or unsubstituted aliphatic group or a substituted or unsubstituted C7-C9 aralkyl group, provided that -COOR15 is not -COOH, or N(R15)2 taken together is a substituted or unsubstituted five or six membered non-aromatic nitrogen- containing heterocyclic group;
R is -H or an alkyl group; R17 is -H; a C1-C6 alkyl group optionally substituted with -OH or -NH2; indolyl; imidazolyl; or phenyl or benzyl optionally substituted with -OH; m is 0 or 1; and
Rings A and B are unsubstituted.
11. The compound of Claim 5 wherein R4 is a cyclohexyl group, a phenyl group or a benzyl group wherein the phenyl or benzyl group represented by R4 is optionally substituted with hydroxy, methoxy, ethoxy, iso-propoxy, methyl, ethyl, propyl, NH2, NHCH3, N(CH3)2, NHCH2CH3, N(CH2CH3)2, N(CH3)(CH2CH3), NH(CH2CH2CH3), N(CH2CH2CH3)2, N(CH3)(CH2CH2CH3) or
N(CH2CH3)(CH2CH2CH3).
12. The compound of Claim 5 wherein R1 is a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted -CH2-(pyridyl) group, a substituted or unsubstituted thienyl group, a substituted or unsubstituted -CH2-(thienyl) group, a substituted or unsubstituted benzothienyl group, a substituted or unsubstituted -CH2-(benzothienyl) group, a substituted or unsubstituted furanyl group; or a substituted or unsubstituted -CH2-(furanyl) group; and R4 is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group; or -ΝR3R4 taken together is a nitrogen-containing non-aromatic heterocyclic ring.
13. The compound of Claim 4 wherein the compound is represented by the following structural formula:
Figure imgf000226_0001
wherein Ring A is optionally substituted at any one or more substitutable ring carbons with a group selected from alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, halogen, cyano and nitro.
14. The compound of Claim 13 wherein R4 is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group; or -ΝR3R4 taken together is a nitrogen-containing non-aromatic heterocyclic ring.
15. The compound of Claim 13 wherein R1 is a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted -CH2-(pyridyl) group, a substituted or unsubstituted thienyl group, a substituted or unsubstituted -CH2-(thienyl) group, a substituted or unsubstituted benzothienyl group, a substituted or unsubstituted -CH2-(benzothienyl) group, a substituted or unsubstituted furanyl group or a substituted or unsubstituted -CH2-(furanyl) group; and R4 is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group; or -ΝR3R4 taken together is a nitrogen-containing non-aromatic heterocyclic ring.
16. The compound of Claim 1 wherein the compound is represented by the following structural formula:
wherein:
Ring A is optionally substituted at any one or more substitutable ring carbons with a group selected from alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, halogen, cyano and nitro;
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; and m is 0 or 1.
17. The compound of Claim 1 wherein the compound is represented by a structural formula selected from:
Figure imgf000228_0002
Figure imgf000228_0003
Figure imgf000229_0001
Figure imgf000230_0001
Figure imgf000230_0002
Figure imgf000230_0003
or a pharmaceutically acceptable salt thereof.
18. A compound represented by the following structural formula:
Figure imgf000230_0004
or a pharmaceutically acceptable salt thereof, wherein: Ring A is unsubstituted;
Ring B is an unsubstituted phenyl, cyclohexyl or cyclopentyl ring fused to Ring A;
R1 is cyclohexyl or phenyl, furanyl, thienyl or pyridyl optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, methylenedioxy, ethylenedioxy, halogen, cyano or nitro;
Figure imgf000231_0001
-C(0)-NHR22, -C(0)-N(R22)2 or -C(0)CH[N(R23)2]R24; R21 is methyl, ethyl, 2-hydroxyethyl or iso-propyl;
R is -H or C1-C4 alkyl or -N(R .22 )2 taken together is N-pyrollidinyl or
N-piperidinyl, provided that R >2 is not -H when R u is -COOR .22.
R .23 is -H, methyl or ethyl;
R .24 : is -H, methyl, ethyl, phenyl, benzyl, 4-hydroxyphenyl or 4- hydroxybenzyl; and s is 0, 1, 2, 3 or 4.
19. A method of treating a subject with a CCR8 mediated disease or condition, said method comprising administering to the subject an effective amount of a compound represented by the following structural formula:
Figure imgf000232_0001
or a pharmaceutically acceptable salt thereof, wherein:
Xi is a covalent bond, C=0 or CRaRb;
X is a covalent bond, O, or NR5;
C=Z is C=0, CH2, C=NH, C=S or absent, provided that when Xi is a covalent bond then C=Z is not CH2, provided that when C=Z is absent then X is a covalent bond, and provided that when X is NR5 and C=Z is C=O then R4 is not an aliphatic or substituted aliphatic group;
Ra and Rb are independently H or a C1-C3 alkyl;
R1 is: i) a substituted or unsubstituted aromatic group; ii) a substituted or unsubstituted non-aromatic ring; or iii) when X is NR5, then NR5-(CH2)mR1, taken together, is optionally a substituted or unsubstituted non-aromatic heterocyclic group;
R2 is -H or a C1-C3 alkyl group;
R3 is -H; and R4 is: i) a substituted or unsubstituted aliphatic group; ii) a substituted or unsubstituted aromatic group; iii) a substituted or unsubstituted non-aromatic ring or a substituted or unsubstituted non-aromatic bridged bicyclic group; or iv) R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group;
R5 is -H, or a C1-C3 alkyl group;
Ring B is a phenyl group or a five or six membered carbocyclic carbocyclic non-aromatic ring fused to Ring A;
Rings A and B are independently substituted or unsubstituted; m is 0, 1, 2 or 3; n is 1 or 2; each substitutable carbon atom of the aromatic group represented by R1 is optionally substituted with a group represented by R10, wherein_R10 is halogen, - R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -O(Ph), substituted -O(Ph), -CH2(Ph), substituted - CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -N02> -CN, -N(R')2, - NR'C02R°, -NR'C(0)R°, -NR'NR'C(0)R°, -N(R')C(0)N(R')2, -NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(0)R°, -C(0)N(R°)2, -OC(O)R°, -OC(0)N(R°)2, -S(0)2R°, -S02N(R -
S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R0, -V-OH, -V-0R0, -V-SH, -V-SR0, -V-N02, - V-CN, -V-N(R')2, -V-NR'CO2R0, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°, -V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-C02R°, -V-C(0)R°, -V-C(O)N(R0)2,
-V-OC(0)R°, -V-OC(0)N(R°)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, - V~NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, or -V-C(=NH)-N(R')2, and each group represented by R10 is independently selected; each substitutable carbon atom of the aliphatic group represented by R4is optionally substituted with a group represented by R11, wherein R11 is halogen, -
R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2-methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -O(Ph), substituted -0(Ph), -CH2(Ph), substituted - CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -N02, -CN, -N(R')2, - NR'C02R°, -NR'C(0)R°, -NR'NR'C(0)R°, -N(R')C(0)N(R')2, -NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°,
-C(0)R°, -C(0)N(R°)2, -OC(0)R°, -OC(0)N(R°)2, -S(0)2R°, -S02N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R0, -V-OH, -V-OR0, -V-SH, -V-SR0, -V-N02, -V-CN, -V-N(R')2, -V-NR'C02R°, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°,
-V-C(0)C(0)R°, -V-C(0)CH2C(0)R°, -V-C(0)R°, -V-C(O)N(R0)2, -V-OC(0)R°, -V-OC(0)N(R°)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, -V-NR'S02N(R')2, N-NR'SO2R0, -V-C(=S)N(R')2, -V-(CH2)yN(R')2, -V-C(=NH)-N(R')2, =NNHR*, =NN(R*)2, =NNHC(0)R*, =NNHCO2(alkyl), =NNHS02 (alkyl), or =NR*, and each group represented by R11 is independently selected; each substitutable carbon atom of the aromatic group represented by R4 is optionally substituted at each substitutable carbon atom with a group represented by R12, wherein R12 is halogen, -R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2- methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -O(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -CN, -NR'C02R°, -NR'NR'C(0)R°, -N(R')C(0)N(R')2,
-NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(0)R°, -OC(0)R°, -OC(0)N(R°)2, -S(0)2R°, -S02N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R°, -V-OH, -V-OR0, -V-SH, -V-SR0, -V-CN, -V-NR'C02R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2,
-V-NR'NR'C02R°, -V-C(0)C(0)R°, N-C(0)CH2C(0)R°, -V-C02R°, N-C(0)R°, -V-OC(0)R°, -V-OC(0)Ν(R°)2, -V-S(0)2R°, -V-S02N(R')2, -V-S(0)R°, - V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2, -V-(CH2)yN(R')2 or -V-C(=NH)-N(R')2, and each group represented by R12 is independently selected; each substitutable carbon atom of: i) the non-aromatic ring represented by
R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR1; iii) the nitrogen-containing non-aromatic heterocyclic group formed from NR3R4; and iv) the non-aromatic bridged bicyclic group represented by R4 is optionally and independently substituted with -R°, -OH, -OR0, -O(haloalkyl), -SH, -SR°, 1,2- methylene-dioxy, 1,2-ethylenedioxy, phenyl (Ph), substituted Ph, -0(Ph), substituted -O(Ph), -CH2(Ph), substituted -CH2(Ph), -CH2CH2(Ph), substituted -CH2CH2(Ph), -CN, -NO2, -N(R')2, -C(0)N(R°)2, -NR'C(0)R°, -NR'C(0)R°, -V-N(R')2, -V-NR'C(0)R°, -V-C(0)N(R°)2, -NR'C02R°, -NR'NR'C(0)R°, -N(R')C(0)N(R')2, -NR'NR'C(0)N(R')2, -NR'NR'C02R°, -C(0)C(0)R°, -C(0)CH2C(0)R°, -C02R°, -C(0)R°, -OC(0)R°, -OC(0)N(R°) , -S(0)2R°,
-S02N(R')2, -S(0)R°, -NR'S02N(R')2, -NR'S02R°, -C(=S)N(R')2, -(CH2)yN(R')2, -C(=NH)-N(R')2, haloalkyl, -V-R°, -V-OH, -V-OR0, -V-SH, -V-SR0, -NR'C(0)R°, -V-NO2, -V-CN, -V-N(R')2, -V-NR'C02R°, -V-NR'C(0)R°, -V-NR'NR'C(0)R°, -V-N(R')C(0)N(R')2, -V-NR'NR'C(0)N(R')2, -V-NR'NR'C02R°, -V-C(0)C(0)R°, -V-C(O)CH2C(O)R0, -V-C02R°, -V-C(0)R°, -V-C(0)N(R°)2, -V-OC(0)R°, -V-OC(0)N(R°)2, -V-S(0)2R°, -V-S02N(R')2,
-V-S(0)R°, -V-NR'S02N(R')2, -V-NR'S02R°, -V-C(=S)N(R')2) -V-(CH2)yN(R')2, -V-C(=NH)-N(R')2, =0, =S, =NNHR*, =NN(R*)2, =NNHC(0)R*, =NNHC02(alkyl), =NNHS02 (alkyl), or =NR*; each R° is independently hydrogen or substituted or unsubstituted aliphatic group, a substituted or unsubstituted cycloaliphatic, a substituted or unsubstituted non-aromatic heterocyclic group or a substituted or unsubstituted aromatic group selected from phenyl, naphthyl, 2-furanyl, 3-furanyl, N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2- oxadiazolyl, 5-oxadiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 1-pyrrolyl, 2- pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3 -pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5- pyrimidyl, 3-pyridazinyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-triazolyl, 5- triazolyl, tetrazolyl, 2-thienyl, 3 -thienyl, carbazolyl, benzimidazolyl, benzothienyl, benzofuranyl, indolyl, quinolinyl, benzotriazolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoquinolinyl, indolyl, isoindolyl, acridinyl, or benzoisazolyl; each R' is independently R°, -C02R°, -S02R° or -C(0)R°; each R* is independently hydrogen, an unsubstituted aliphatic group or a substituted aliphatic group;
V is a C1-C6 alkylene group; each substitutable carbon atom of : i)) the aliphatic, cycloaliphatic, non- aromatic heterocyclic group and aromatic group represented by R°; and ii) the aliphatic group represented by R* is optionally and independently substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, aminoalkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl; each substitutable nitrogen atom of: i) the non-aromatic ring represented by R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR1; iii) the nitrogen-containing non-aromatic heterocyclic group formed from NR3R4; iv) the non-aromatic heterocyclic group represented by R4; and v) the non- aromatic bridged bicyclic group represented by R4 is optionally and independently substituted with R+, -N(R+)2, -C(0)R+, -C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N(R+)2, -C(=S)N(R+)2, -C(=NH)-N(R+)2, -NR+ S02 R+, -C(0)-NHR+, -C(0)-N(R+)2j -C(0)-CH[N(R+)2]R+ or -C(0)-CH[OR+]R+; each R+ is independently hydrogen, an unsubstituted heteroaryl or an aliphatic, cycloaliphatic, non-aromatic heterocyclic group, phenyl or benzyl group, wherein each substitutable carbon atom of the aliphatic, cycloaliphatic, non- aromatic heterocyclic ring, phenyl or benzyl group represented by R+ is optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl or N(R+)2 is a non-aromatic heterocyclic group; and each substitutable nitrogen atom of the non-aromatic heterocyclic group represented by R+ is optionally substituted with alkyl, alkoxycarbonyl, alkylcarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl.
20. The method of Claim 19 wherein the compound is represented by the following structural formula:
Figure imgf000236_0001
wherein:
C=Z is C=0, CH2,C=NH or C=S; Rings A and B are optionally substituted with alkyl, halolkyl, alkoxy, haloalkoxy, hydroxy, halogen, cyano or nitro;
R4 is a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aromatic group or a substituted or unsubstituted non-aromatic ring; each substitutable nitrogen atom of: i) the non-aromatic ring represented by R1 or R4; ii) the non-aromatic heterocyclic group formed from NR5(CH2)mR'; iii) the nitrogen-containing non-aromatic heterocyclic group formed from R3, R4 and the nitrogen atom to which R3 and R4 are bonded; and iv) the non-aromatic heterocyclic group represented by R° are selected from R+, -N(R+)2, -C(0)R+, - C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N +fe, -C(=S)N(R+)2,
-C(=NH)-N(R+)2 and -NR+ S02 R+; and each R+ is independently hydrogen, an unsubstituted heteroaryl or an unsubstituted non-aromatic heterocyclic ring or an aliphatic, phenyl or benzyl group optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
21. The method of Claim 19 wherein the CCR8 mediated disease or condition is asthma, atopic dermatitis, allergic rhinitis, systemic anaphylaxis, a hypersensitivity response, a drug allergy, an insect sting allergy, dermatitis, eczema, atopic dermatitis, allergic contact dermatitis, urticaria, rheumatoid arthritis, osteoarthritis, inflammatory bowel disease multiple sclerosis, systemic lupus erythematosus, myasthenia gravis, juvenile onset diabetes, glomerulonephritis, autoimmune thyroiditis, Behcet's disease or graft rejection.
22. The method of Claim 21 wherein the CCR8 mediated disease or condition is asthma.
23. The method of Claim 21 wherein:
C=Z is C=0 and Xj is a bond; X is a bond;
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group optionally substituted with one or more groups R10;
R2 is -H;
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1; and n is 2.
24. The method of Claim 23 wherein the compound is represented by the following structural formula:
Figure imgf000238_0001
wherein Rings A and B are unsubstituted.
25. The method of Claim 19 wherein the compound is represented by the following structural formula:
Figure imgf000239_0001
wherein:
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1;
Rings A and B are unsubstituted; each substitutable nitrogen atom in: i) the non-aromatic heterocyclic group formed from -NR3R4; and ii) the non-aromatic ring represented by R4 are R+, - N(R+)2, -C(0)R+, -C02 R+, -C(0)C(0)R+, -C(0)CH2 C(0)R+, -S02 R+, -S02 N(R+)2, -C(=S)N(R+)2, -C(=NH)-N(R+)2 and -NR+ S02 R+; and each R+ is independently hydrogen, an unsubstituted heteroaryl or an unsubstituted non-aromatic heterocyclic ring or an aliphatic, phenyl or benzyl group optionally substituted with amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
26. The method of Claim 19 wherein the compound is represented by the following structural formula:
Figure imgf000240_0001
wherein:
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R ( 10 ;.
R3 is -H and R4 is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; m is 0 or 1; and
Rings A and B are unsubstituted.
27. The method of Claim 24 wherein R4 is a substituted or unsubstituted non-aromatic ring.
28. The method of Claim 27 wherein R4 is a piperidinyl group or an N-substituted piperidinyl group.
29. The method of Claim 19 wherein the compound is represented by the following structural formula:
Figure imgf000241_0001
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H;
R4 is a piperidinyl group N-substituted with R15, -C(0)R15, -C(0)OR15, -C(0)-ΝHR15, -C(0)-N(R15 2, or -C(0)CH[N(R16)2]R17; each substitutable carbon of the piperidinyl group represented by R4 is optionally and independently substituted with an aliphatic group or substituted aliphatic group;
R15 is -H, substituted or unsubstituted_a non-aromatic ring, or a substituted or unsubstituted aliphatic group or a substituted or unsubstituted C7-C9 aralkyl group, provided that -COOR15 is not -COOH, or N(R15)2 taken together is a substituted or unsubstituted five or six membered non-aromatic nitrogen- containing heterocyclic group;
R16 is -H or an alkyl group;
R17 is -H; a C1-C6 alkyl group optionally substituted with -OH or -NH2; indolyl; imidazolyl; or phenyl or benzyl optionally substituted with -OH; m is 0 or 1; and
Rings A and B are unsubstituted.
30. The method of Claim 24 wherein R4 is a cyclohexyl group, a phenyl group or a benzyl group wherein the phenyl or benzyl group represented by R4 is optionally substituted with hydroxy, methoxy, ethoxy, iso-propoxy, methyl, ethyl, propyl, NH2, NHCH3, N(CH3)2, NHCH2CH3, N(CH2CH3)2, N(CH3)(CH2CH3), NH(CH2CH2CH3), N(CH2CH2CH3)2, N(CH3)(CH2CH2CH3) or N(CH2CH3)(CH2CH2CH3).
31. The method of Claim 24 wherein R1 is a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted -CH2-(pyridyl) group, a substituted or unsubstituted thienyl group, a substituted or unsubstituted -CH2-(thienyl) group, a substituted or unsubstituted benzothienyl group, a substituted or unsubstituted -CH2-(benzothienyl) group, a substituted or unsubstituted furanyl group; or a substituted or unsubstituted -CH2-(furanyl) group; and R4 is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group; or -ΝR3R4 taken together is a nitrogen-containing non-aromatic heterocyclic ring.
32. The method of Claim 23 wherein the compound is represented by the following structural formula:
Figure imgf000242_0001
wherein Ring A is optionally substituted at any one or more substitutable ring carbons a group selected from alkyl, hydroxy, alkoxy, halogen, cyano or nitro.
33. The method of Claim 32 wherein R1 is a substituted or unsubstituted cyclohexyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted -CH2-(pyridyl) group, a substituted or unsubstituted thienyl group, a substituted or unsubstituted -CH2-(thienyl) group, a substituted or unsubstituted benzothienyl group, a substituted or unsubstituted -CH2-(benzothienyl) group, a substituted or unsubstituted furanyl group or a substituted or unsubstituted - CH2-(furanyl) group; and R4 is a piperidinyl group, an N-substituted piperidinyl group, a cyclohexyl group, a substituted cyclohexyl group, an unsubstituted phenyl group, an unsubstituted benzyl group or a phenyl or benzyl group substituted with an electron donating group; or -ΝR3R4 taken together is a nitrogen-containing non-aromatic heterocyclic ring.
34. The method of Claim 19 wherein the compound is represented by the following structural formula:
Figure imgf000243_0001
wherein:
Ring A is optionally substituted at any one or more substitutable ring carbons a group selected from alkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, halogen, cyano or nitro;
R1 is a substituted or unsubstituted cycloalkyl group or an aromatic group substituted at zero, one or more substitutable carbon atoms by R10;
R3 is -H or R3 and R4 taken together with the nitrogen atom to which they are bonded are a substituted or unsubstituted nitrogen-containing non-aromatic heterocyclic group; R is a substituted or unsubstituted non-aromatic ring or a phenyl group or benzyl group optionally substituted with one or more groups R12; and m is 0 or 1.
35. A method of treating a subject with a CCR8 mediated disease or condition, said method comprising administering to the subject an effective amount of a compound represented by the following structural formula:
Figure imgf000244_0001
or a pharmaceutically acceptable salt thereof, wherein:
Ring A is substituted;
Ring B is an unsubstituted phenyl, cyclohexyl or cyclopentyl ring fused to Ring A;
R1 is cyclohexyl or phenyl, furanyl, thienyl or pyridyl optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, methylenedioxy, ethylenedioxy, halogen, cyano or nitro;
Figure imgf000244_0002
Figure imgf000245_0001
-C(0)-NHR22, -C(0)-N(R22)2 or -C(0)CH[N(R23)2]R24;
R21 is methyl, ethyl, 2-hydroxyethyl or iso-propyl;
R22 is -H or C1-C4 alkyl or -N(R22)2 taken together is N-pyrollidinyl or N-piperidinyl, provided that R22 is not -H when R20 is -COOR22;
R23 is -H, methyl or ethyl;
R24 is -H, methyl, ethyl, phenyl, benzyl, 4-hydroxyphenyl or 4- hydroxybenzyl; and s is 0, 1, 2, 3 or 4. 36. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and the compound of Claim 1.
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US7329755B2 (en) 2008-02-12
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