WO2003099814A1 - Calcium receptor modulating agents - Google Patents

Calcium receptor modulating agents Download PDF

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Publication number
WO2003099814A1
WO2003099814A1 PCT/US2003/016384 US0316384W WO03099814A1 WO 2003099814 A1 WO2003099814 A1 WO 2003099814A1 US 0316384 W US0316384 W US 0316384W WO 03099814 A1 WO03099814 A1 WO 03099814A1
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Prior art keywords
alkyl
haloalkyl
aryl
compound
phenyl
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PCT/US2003/016384
Other languages
French (fr)
Inventor
Michael G. Kelly
Shimin Xu
Ning Xi
Robert Townsend
David J. Semin
Chiara Ghiron
Thomas Coutler
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Amgen, Inc.
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Priority to AT03736701T priority Critical patent/ATE544762T1/en
Priority to AU2003237235A priority patent/AU2003237235B2/en
Priority to JP2004507471A priority patent/JP4642461B2/en
Priority to EP03736701A priority patent/EP1509518B1/en
Priority to ES03736701T priority patent/ES2378759T3/en
Priority to MXPA04011469A priority patent/MXPA04011469A/en
Priority to CA002485685A priority patent/CA2485685C/en
Publication of WO2003099814A1 publication Critical patent/WO2003099814A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
    • A61P5/20—Drugs for disorders of the endocrine system of the parathyroid hormones for decreasing, blocking or antagonising the activity of PTH
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
    • A61P5/22—Drugs for disorders of the endocrine system of the parathyroid hormones for decreasing, blocking or antagonising the activity of calcitonin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • 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
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • 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
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • 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
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12—Radicals substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C07D209/88—Carbazoles; Hydrogenated carbazoles 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 carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
    • C07D413/04—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
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems

Definitions

  • Extracellular calcium ion concentration is involved in a variety of biological processes, such as blood clotting, nerve and muscle excitability and bone formation (Cell Calcium 11:319, 1990).
  • Calcium ion receptors which are present on the membranes of various cells in the body, such as parathyroid and kidney cells (Nature 366:574, 1993; J. Bone Miner. Res. 9, Supple. 1, s282, 1994; J. Bone Miner. Res. 9, Supple. 1, s409, 1994; Endocrinology 136:5202, 1995), are important to the regulation of the extracellular calcium ion concentration.
  • concentration of extracellular calcium ion regulates the bone resorption by osteoclasts (Bioscience Reports 10:493, 1990), secretion of parathyroid hormone (PTH) from parathyroid cells and secretion of calcitonin from C-cells (Cell Calcium 11:323, 1990).
  • Parathyroid hormone (PTH) is an important factor in regulating extracellular calcium ion concentration. Secretion of PTH increases extracellular calcium ion concentration by acting on various cells, such as bone and kidney cells, and the extracellular calcium ion concentration reciprocally inhibits the secretion of PTH by acting on parathyroid cells.
  • the present invention relates to selected calcimimetic compounds and pharmaceutically acceptable salts thereof.
  • the invention compounds advantageously reduce or inhibit PTH secretion. Therefore, this invention also encompasses pharmaceutical compositions, methods for reducing or inhibiting PTH secretion and methods for treatment or prophylaxis of diseases associated with bone disorders, such as osteoporosis, or associated with excessive secretion of PTH, such as hyperparathyroidism.
  • the subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
  • the compounds of the invention are represented by the following general structure
  • the invention provides compounds of Formula (I):
  • R 1 is R b ;
  • R 2 is -salkyl or C ⁇ - 4 haloalkyl
  • R 3 is H, C ⁇ - 4 haloalkyl or C ⁇ - 8 alkyl
  • R 4 is H, C ⁇ haloalkyl or C ⁇ - 8 alkyl
  • R a is, independently, at each instance, H, C ⁇ - -aloalkyl or C ⁇ - 6 alkyl
  • R b is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from -ealkyl, halogen, C ⁇ haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro;
  • R c is, independently, at each instance, C ⁇ - 6 alkyl, C ⁇ - 4 haloalkyl, phenyl or benzyl;
  • R 1 is phenyl substituted by 0, 1, 2 or 3 substituents selected from C ⁇ - 6 alkyl, halogen, C ⁇ - 4 haloalkyl, -OC ⁇ . 6 alkyl, cyano and nitro.
  • R 1 is benzyl substituted by 0, 1, 2 or 3 substituents selected from C ⁇ - 6 alkyl, halogen, C ⁇ - haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro.
  • R 1 is naphthyl substituted by 0, 1, 2 or 3 substituents selected from C ⁇ - 6 alkyl, halogen, C ⁇ haloalkyl, -OCi- 6 alkyl, cyano and nitro.
  • R 1 is a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 0, 1, 2 or 3 substituents selected from C ⁇ alkyl, halogen, Ci.- t haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro.
  • R 3 and R 4 are H.
  • R 5 is H.
  • R 6 is H.
  • R is H
  • X is -NR d -.
  • ⁇ is a double bond
  • Y is -CR a R 6 - or -NR d -; and Z is -CR a R 7 - or -NR d -.
  • the invention provides a compound of Formula (II):
  • R > ⁇ 1 . is R D ;
  • R 3 is H, C ⁇ - 4 haloalkyl or d. 8 alkyl;
  • R 4 is H, Ci- 4 haloalkyl or C ⁇ - 8 alkyl
  • R a is, independently, at each instance, H, C ⁇ - 4 haloalkyl or d- 6 alkyl;
  • R b is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from d- 6 alkyl, halogen, C ⁇ - 4 haloalkyl, -OC ⁇ - alkyl, cyano and nitro;
  • R c is, independently, at each instance, d- 6 alkyl, d- 4 haloalkyl, phenyl or benzyl;
  • the compound in another embodiment, in conjunction with any one of the above and below embodiments, has the structure
  • R 1 is R ;
  • R 2 is d, 8 alkyl or d- 4 haloalkyl
  • R 3 is H, d- 4 haloalkyl or d- 8 alkyl
  • R 4 is H, d- 4 haloalkyl or C ⁇ - 8 alkyl
  • R is, independently, at each instance, H, C ⁇ - 4 haloalkyl or C ⁇ - 6 alkyl;
  • R is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from C ⁇ - 6 alkyl, halogen, C ⁇ - 4 haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro;
  • R c is, independently, at each instance, C ⁇ - 6 alkyl, phenyl or benzyl;
  • R 1 is phenyl substituted by 2 or 3 substituents selected from d- 6 alkyl, halogen, d- 4 haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro.
  • R 1 is benzyl substituted by 1, 2 or 3 substituents selected from d- 6 alkyl, halogen, C ⁇ - 4 haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro.
  • R 1 is naphthyl substituted by 1, 2 or 3 substituents selected from C ⁇ - 6 alkyl, halogen, C ⁇ - 4 haloalkyl, -Od- 6 alkyl, cyano and nitro.
  • R 1 a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 1, 2 or 3 substituents selected from d- 6 alkyl, halogen, d- 4 haloalkyl, -OC ⁇ - 6 alkyl, cyano and nitro.
  • one of R 3 or R 4 is C ⁇ - 4 haloalkyl or d- 8 a ⁇ kyl.
  • R 6 is not H.
  • R 7 is not H.
  • Another aspect of the invention involves a pharmaceutical composition comprising a pharmaceutically acceptable amount of a compound according to any one of Claims 1-22 and a pharmaceutically acceptable diluent or carrier.
  • Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, as a medicament.
  • Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, in the manufacture of a medicament for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH.
  • Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, in the manufacture of a medicament for the treatment of osteoporosis or hyperparathyroidism.
  • Another aspect of the invention involves a method of using a compound in conjunction with any one of the above and below embodiments, for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH.
  • Another aspect of the invention involves a method of using a compound in conjunction with any one of the above and below embodiments, for the treatment of osteoporosis or hyperparathyroidism.
  • Another aspect of the invention involves a process for making a compound in conjunction with any one of the above and below embodiments comprising the step of: reacting a compound having the structure
  • the compounds may also be synthesized as follows: LiAIH 4
  • alkyl and the prefix “alk” refer to alkyl groups or substituents wherein the carbon atoms are in a branched, cyclical or linear relationship or any combination of the three.
  • C v - W alkyl means an alkyl group comprising from V to W carbon atoms.
  • the alkyl groups described in this section contain from 1 to 10 carbon atoms unless otherwise specified and may also contain a double or triple bond. Examples of d- 6 alkyl include, but are not limited to the following:
  • Aryl means a carbocyclic aromatic ring or ring system.
  • aryl groups include phenyl, naphthyl, indenyl, anthrancenyl, 9-(9-phenylfluorenyl), phenanthrenyl, and the like.
  • Halogen means a halogen atom selected from F, Cl, Br and I.
  • Haloalkyl means an alkyl group, as described above, wherein any number— at least one— of the hydrogen atoms attached to the alkyl chain are replaced by F, Cl, Br or I.
  • Heterocycle means a ring comprising at least one carbon atom and at least one other atom selected from N, O and S. Heterocyclic groups can be saturated, unsaturated or aromatic. Aromatic heterocyclic groups are also referred to as "heteroaryl” rings or ring systems. Examples of heterocycles that may be found in the claims include, but are not limited to, the following:
  • “Pharmaceutically acceptable salt” means a salt prepared by conventional means, and are well known by those skilled in the art.
  • the “pharmaceutically acceptable salts” include basic salts of inorganic and organic acids, including but not limited to hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulphonic acid, ethanesulfonic acid, malic acid, acetic acid, oxalic acid, tartaric acid, citric acid, lactic acid, fumaric acid, succinic acid, maleic acid, salicylic acid, benzoic acid, phenylacetic acid, mandelic acid and the like.
  • suitable pharmaceutically acceptable cation pairs for the carboxy group are well known to those skilled in the art and include alkaline, alkaline earth, ammonium, quaternary ammonium cations and the like.
  • pharmaceutically acceptable salts see infra and Berge et al., J. Pharm. Sci. 66:1 (1977).
  • leaving group generally refers to groups readily displaceable by a nucleophile, such as an amine, a thiol or an alcohol nucleophile. Such leaving groups are well known in the art. Examples of such leaving groups include, but are not limited to, N-hydroxysuccinimide, N-hydroxybenzotriazole, halides, triflates, tosylates and the like. Preferred leaving groups are indicated herein where appropriate.
  • Protecting group generally refers to groups well known in the art which are used to prevent selected reactive groups, such as carboxy, amino, hydroxy, mercapto and the like, from undergoing undesired reactions, such as nucleophilic, electrophilic, oxidation, reduction and the like.
  • amino protecting groups include, but are not limited to, aralkyl, substituted aralkyl, cycloalkenylalkyl and substituted cycloalkenyl alkyl, allyl, substituted allyl, acyl, alkoxycarbonyl, aralkoxycarbonyl, silyl and the like.
  • aralkyl examples include, but are not limited to, benzyl, ortho- methylbenzyl, trityl and benzhydryl, which can be optionally substituted with halogen, alkyl, alkoxy, hydroxy, nitro, acylamino, acyl and the like, and salts, such as phosphonium and ammonium salts.
  • cycloalkenylalkyl or substituted cycloalkylenylalkyl radicals preferably have 6-10 carbon atoms, include, but are not limited to, cyclohexenyl methyl and the like.
  • Suitable acyl, alkoxycarbonyl and aralkoxycarbonyl groups include benzyloxycarbonyl, t- butoxycarbonyl, iso-butoxycarbonyl, benzoyl, substituted benzoyl, butyryl, acetyl, tri-fluoroacetyl, tri-chloro acetyl, phthaloyl and the like.
  • a mixture of protecting groups can be used to protect the same amino group, such as a primary amino group can be protected by both an aralkyl group and an aralkoxycarbonyl group.
  • Amino protecting groups can also form a heterocyclic ring with the nitrogen to which they are attached, for example, l,2-bis(methylene)benzene, phthalimidyl, succinimidyl, maleimidyl and the like and where these heterocyclic groups can further include adjoining aryl and cycloalkyl rings.
  • the heterocyclic groups can be mono-, di- or tri-substituted, such as nitrophthalimidyl.
  • Amino groups may also be protected against undesired reactions, such as oxidation, through the formation of an addition salt, such as hydrochloride, toluenesulfonic acid, trifluoroacetic acid and the like.
  • Many of the amino protecting groups are also suitable for protecting carboxy, hydroxy and mercapto groups.
  • Alkyl groups are also suitable groups for protecting hydroxy and mercapto groups, such as tert- butyl.
  • Silyl protecting groups are silicon atoms optionally substituted by one or more alkyl, aryl and aralkyl groups. Suitable silyl protecting groups include, but are not limited to, trimethylsilyl, triethylsilyl, tri-isopropylsilyl, tert- butyldimethylsilyl, dimethylphenylsilyl, 1 ,2-bis(dimethylsilyl)benzene, l,2-bis(dimethylsilyl)ethane and diphenylmethylsilyl.
  • Silylation of an amino groups provide mono- or di-silylamino groups. Silylation of aminoalcohol compounds can lead to a N,N,O-tri-silyl derivative.
  • silyl function from a silyl ether function is readily accomplished by treatment with, for example, a metal hydroxide or ammonium fluoride reagent, either as a discrete reaction step or in situ during a reaction with the alcohol group.
  • Suitable silylating agents are, for example, trimethylsilyl chloride, tert-butyl-dimethylsilyl chloride, phenyldimethylsilyl chloride, diphenylmethyl silyl chloride or their combination products with imidazole or DMF.
  • Methods for silylation of amines and removal of silyl protecting groups are well known to those skilled in the art.
  • Methods of preparation of these amine derivatives from corresponding amino acids, amino acid amides or amino acid esters are also well known to those skilled in the art of organic chemistry including amino acid/amino acid ester or aminoalcohol chemistry.
  • Protecting groups are removed under conditions which will not affect the remaining portion of the molecule. These methods are well known in the art and include acid hydrolysis, hydrogenolysis and the like.
  • a preferred method involves removal of a protecting group, such as removal of a benzyloxycarbonyl group by hydrogenolysis utilizing palladium on carbon in a suitable solvent system such as an alcohol, acetic acid, and the like or mixtures thereof.
  • a t- butoxycarbonyl protecting group can be removed utilizing an inorganic or organic acid, such as HC1 or trifluoroacetic acid, in a suitable solvent system, such as dioxane or methylene chloride.
  • the resulting amino salt can readily be neutralized to yield the free amine.
  • Carboxy protecting group such as methyl, ethyl, benzyl, tert-butyl, 4-methoxy ⁇ henylmethyl and the like, can be removed under hydrolysis and hydrogenolysis conditions well known to those skilled in the art.
  • Prodrugs of the compounds of this invention are also contemplated by this invention.
  • a prodrug is an active or inactive compound that is modified chemically through in vivo physiological action, such as hydrolysis, metabolism and the like, into a compound of this invention following administration of the prodrug to a patient.
  • the suitability and techniques involved in making and using prodrugs are well known by those skilled in the art.
  • For a general discussion of prodrugs involving esters see Svensson and Tunek Drug Metabolism Reviews 165 (1988) and Bundgaard Design of Prodrugs, Elsevier (1985).
  • Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl).
  • esters such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl).
  • Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989)). Also, drugs containing an acidic NH group, such as imidazole, imide, indole and the like, have been masked with N- acyloxymethyl groups (Bundgaard Design of Prodrugs, Elsevier (1985)).
  • Preferred compounds of the invention include:
  • Method B The aldehyde (1.6 mmol) is dissolved in methanol (5 mL) and the amine (1.9 mmol) is added. The reaction is heated to reflux for 10 minutes then left to cool overnight until imine formation is complete (as monitored by LCMS). Solid-supported cyanoborohydride is added (prepared according to Sande, A. R.; Jagadale, M. H.; Mane, R. B.; Salunkhe, M. M.; Tetrahedron Lett. (1984), 25(32), 3501-4) (ca 2.5mmol/g; 3.1 mmol) and the mixture is heated at 50 °C for 15 hours or until reduction is complete (as monitored by LCMS).
  • the title compound was prepared by the method C.
  • the title compound was prepared by the method C.
  • the title compound was prepared by the method C.
  • Example 4A Ethyl 2-ethylbenzotriazole-5-carboxylate Benzotriazole-5-carboxylic acid (1.5 g, 9.2 mmol) and ethyl iodide (1.61 mL, 20.2 mmol) were dissolved in DMF (20 mL and sodium hydride (0.800 g, 20.2 mmol, 60% suspension in mineral oil) was added. The mixture was stirred under nitrogen at 55 °C for one hour then the reaction was cooled and quenched with water, diluted with ethyl acetate and washed with water. The organic phase was separated and dried over sodium sulfate.
  • Ethyl 2-etliylbenzotriazole-5-carboxylate (0.7g, 3.06 mmol) was dissolved in dry toluene (10 mL) and cooled to 0 °C under nitrogen. A solution of DIBAL-H (1.5M in toluene, 3 mL, 4.5 mmol) was then added dropwise to the cooled solution over 15 minutes. The reaction was stirred at 0 °C for one hour when further DIBAL-H (1.5 mL, 2.25 mmol) was added. A further aliquot of DIBAL-H (0.75 mL, 1.12 mmol) was added after 2 hours and the reaction was stirred for further 30 min.
  • DIBAL-H 1.5M in toluene, 3 mL, 4.5 mmol
  • Example 4C 2-Ethyl-5-formylbenzotriazole.
  • the crude alcohol from the previous step (440 mg, 2.49 mmol) was dissolved in acetone (10 mL) and treated with manganese dioxide (2.6 g, 29.9 mmol). The reaction was stirred at room temperature for 72 hours then the solid filtered off to afford the aldehyde which was used without further purification
  • Example 7A 6-Methoxy-l,2,3,4-tetrahydrocarbazole-3-carboxylic acid ethyl ester.
  • Example 7B 6-Methoxycarbazole-3-carboxylic acid ethyl ester.
  • Example 7E 9-Ethyl-6-methoxycarbazole-3-carboxaldehyde A solution of 9-ethyl-3-hydroxymethyl-6-methoxycarbazole (0.305 g, 1.2 mmol) in acetone (5 mL) was treated with MnO 2 (0.52 g, 6 mmol) and the reaction stirred at room temperature for 60 hours. The reaction mixture was filtered and the solvent evaporated under reduced pressure. The crude was purified by column chromatography (heptane/ethyl acetate 5/1) to afford 0.190 mg of the title compound.
  • Example 10C l-ethylcyclopent[b]indole-5-carboxaldehyde A solution of 7-cyano-4-ethyl-l,2,3,4-tetrahydrocyclopent[b]indole (0.28 g, 1.33 mmol) in dichloromethane (15 mL) was cooled in an ice-bath then treated with DIBAL-H (0.189 g, 1.33 mmol). The reaction was then allowed to reach room temperature and was stirred for 15 hours before diluting with dichloromethane and pouring into a saturated solution of sodium potassium tartrate. The organic layer was separated then washed with brine.
  • Example 10D (R)-N-(l-((Phenyl)ethyl)-N-((l-ethylcyclopent[b]indol-5- yl)methyl)amine
  • Example 11 A Methyl l-methylbenzimidazole-5-carboxylate
  • a solution of methyl 3-amino-4-methylaminobenzoate (prepared as in DE 1990390463 Al) (2.57 g, 14 mmol) in trimethyl orthoformate (50 mL) was refluxed for 16 hours. The solvent was then removed under reduced pressure to afford 2.31 g of product.
  • C ⁇ oH ⁇ 0 ⁇ 2 O 2 Mass (calculated): [190]; (found): [M+H ⁇ ] 191.
  • Example 11C l-Methylbenzimidazole-5-carboxaldehyde A solution of 5-hydroxymethyl-l-methylbenzimidazole (0.8 g, 4 mmol) in acetone (40 mL) was treated with MnO 2 (4 g) and the mixture was stirred for 3 days. The solid was filtered off and the solvent removed under reduced pressure to give 0.63 g of product.
  • Example 13A 2-Ethoxycarbonyl-l,2,5,6-tetrahydropyrido[3,4-b]indole-8- carboxylic acid
  • Example 13B Ethyl 5-ethyl-2-ethoxycarbonyl-l,2,5,6-tetrahydropyrido[3,4- b]indole-8-carboxylate
  • Example 13D 5-Ethyl-2-methyl-l ,2,5,6-tetrahydropyrido[3,4-b]indole-8- carboxaldehyde
  • a solution of 5-Ethyl-8-hydroxymethyl-2-methyl-l,2,3,4-tetrahydropyrido[4,3- b]indole (0.73 g, 2.98 mmol) in acetone (40 mL) was treated with MnO 2 (3.66 g) and stirred at room temperature for 72 hours. The solid was filtered and the solvent removed in vacuo to afford 0.67 g of title compound.
  • Example 13E (R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-2-methyl-l,2,5,6- tetrahydropyrido[3,4-b]indole-8-yl)methyl)amine
  • Example 19A Methyl l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxylate Tetrahydro-4H-pyran-4-one (1.3 g, 13 mmol), 4-amino-3-iodobenzoic acid methyl ester (3.46 g, 12.5 mmol), DABCO (4.37 g, 39 mmol), MgSO 4 (2.35 g, 19.5 mmol) and Pd(OAc) 2 (0.15 g, 0.00065 mol) were dissolved in DMF (18 mL) and heated under nitrogen at 105 °C for 2 days. The reaction mixture was then partitioned between ethyl acetate and water, and extracted.
  • Example 19C 5-Ethyl-8-hydroxymethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole
  • Ethyl l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxylate (0.56 g, 2.16 mmol) was dissolved in dry THF (30 mL) and lithium aluminum hydride (1M in THF, 10.82 mL, 10.82 mmol) was added via syringe. The mixture was heated to reflux for one hour then cooled and NaOH (5% aqueous solution, 2.67 mL) was added. The mixture was filtered through diatomaceous earth and the solvent was removed to afford 0.5 g of title compound.
  • Example 19D 5-Ethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxyaldehyde 5-ethyl-8-hydroxymethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole (0.5 g, 2.16 mmol) was dissolved in acetone (20 mL) and MnO 2 (2.6 g) was added. The mixture was stirred for 24 hours then filtered and the filtrate concentrated in vacuo to afford 0.36 g of title compound.
  • Example 22A 9-(3-chloropropyl)carbazole Prepared as in WO9634863. C ⁇ 5 H ⁇ 4 ClN Mass (calculated): [243].
  • Example 22B 9-(3-(N,N-dimethylamino)propyl)carbazole 9-(3-chloropropyl)carbazole (2.5 g, 10 mmol) was dissolved in acetonitrile (50 mL) in a pressure tube and dimethylamine hydrochloride (12.2 g, 150 mmol, followed by K 2 CO 3 (20.8 g, 150 mmol) and potassium iodide (0.2 g, 1 mmol) were added and the mixture was stirred at room temperature for 7 days, then filtered and the filtrate concentrated in vacuo. The crude was purified by column chromatography (eluting with 5% methanol in dichloromethane) to afford 1.87 g of the title compound. C ⁇ 7 H 2 o ⁇ 2
  • Example 22C 9-(3-(N,N-Dimethylamino)propyl)carbazole-3-carboxyaldehyde A solution of 9-(3-(N,N-dimethylamino)propyl)carbazole (0.37 g, 1.45 mmol) was dissolved in dichloromethane (6 mL) and the solution cooled to 0 °C. Aluminum trichloride (0.39 g, 2.91 mmol) was then added and the mixture was stirred for 10 minutes.
  • the activities of the compounds of the present invention on calcium receptors were measured.
  • the measurement was performed in accordance with the method described in Example 4 of Nemeth et al., PCT/US95/13704 (International Publication No. WO96/12697) herein incorporated by reference.
  • a 4.0-kb Notl-Hind-XT fragment of the human parathyroid cell Ca 24" receptor (hPCaR) cD ⁇ A was subcloned into the mammalian expression vector pCEP4 (Invitrogen) containing the hygromycin-resistant gene as a selectable marker. This plasmid was transfected into HEK 293 cells by calcium phosphate precipitation. Transfected cells were grown in Dulbecco's modified Eagle's medium containing 10% fetal bovine serum and hygromycin (200 ⁇ g/mL).
  • Hygromycin-resistant colonies were subcloned and assayed for hPCaR mR ⁇ A by solution hybridization using a 32 P-labeled R ⁇ A probe complementary to the (4.0 kb) hPCaR sequence (Garrett, et al., J. Biol. Chem. 270, 12919-12925 (1995)).
  • Clone 7 was used to assess the effects of compounds on [Ca 2+ ]j. This stably transfected cell line is termed HEK 293 4.0-7.
  • the cells were recovered from tissue culture flasks by brief treatment with 0,02%
  • the compounds of the present invention may be administered orally, parentally, by inhalation spray, rectally, or topically in dosage unit formulations containing conventional pharmaceutically acceptable carriers, adjuvants, and vehicles.
  • parenteral as used herein includes, subcutaneous, intravenous, intramuscular, intrasternal, infusion techniques or intraperitoneally.
  • Treatment of diseases and disorders herein is intended to also include the prophylactic administration of a compound of the invention, a pharmaceutical salt thereof, or a pharmaceutical composition of either to a subject (i.e., an animal, preferably a mammal, most preferably a human) believed to be in need of preventative treatment, such as, for example, pain, inflammation and the like.
  • a subject i.e., an animal, preferably a mammal, most preferably a human
  • the dosage regimen for treating the disclosed diseases with the compounds of this invention and/or compositions of this invention is based on a variety of factors, including the type of disease, the age, weight, sex, medical condition of the patient, the severity of the condition, the route of administration, and the particular compound employed. Thus, the dosage regimen may vary widely, but can be determined routinely using standard methods. Dosage levels of the order from about 0.01 mg to 30 mg per kilogram of body weight per day, preferably from about 0.1 mg to 10 mg/kg, more preferably from about 0.25 mg to 1
  • the pharmaceutically active compounds of this invention can be processed in accordance with conventional methods of pharmacy to produce medicinal agents for administration to patients, including humans and other mammals.
  • the pharmaceutical composition may be in the form of, for example, a capsule, a tablet, a suspension, or liquid.
  • the pharmaceutical composition is preferably made in the form of a dosage unit containing a given amount of the active ingredient.
  • these may contain an amount of active ingredient from about 1 to 2000 mg, preferably from about 1 to 500 mg, more preferably from about 5 to 150 mg.
  • a suitable daily dose for a human or other mammal may vary widely depending on the condition of the patient and other factors, but, once again, can be determined using routine methods.
  • the active ingredient may also be administered by injection as a composition with suitable carriers including saline, dextrose, or water.
  • suitable carriers including saline, dextrose, or water.
  • the daily parenteral dosage regimen will be from about 0.1 to about 30 mg/kg of total body weight, preferably from about 0.1 to about 10 mg/kg, and more preferably from about 0.25 mg to 1 mg/kg.
  • Injectable preparations such as sterile injectable aqueous or oleaginous suspensions, may be formulated according to the known are using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1,3-butanediol.
  • a non-toxic parenterally acceptable diluent or solvent for example as a solution in 1,3-butanediol.
  • the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed, including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid find use in the preparation of injectables.
  • Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient such as cocoa butter and polyethylene glycols that are solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum and release the drug.
  • a suitable topical dose of active ingredient of a compound of the invention is 0.1 mg to 150 mg administered one to four, preferably one or two times daily.
  • the active ingredient may comprise from 0.001% to 10% w/w, e.g., from 1% to 2% by weight of the formulation, although it may comprise as much as 10% w/w, but preferably not more than 5% w/w, and more preferably from 0.1% to 1% of the formulation.
  • Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin (e.g., liniments, lotions, ointments, creams, or pastes) and drops suitable for administration to the eye, ear, or nose.
  • liquid or semi-liquid preparations suitable for penetration through the skin e.g., liniments, lotions, ointments, creams, or pastes
  • drops suitable for administration to the eye, ear, or nose e.g., liniments, lotions, ointments, creams, or pastes
  • the compounds of this invention are ordinarily combined with one or more adjuvants appropriate for the indicated route of administration.
  • the compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, stearic acid, talc, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulphuric acids, acacia, gelatin, sodium alginate, polyvinyl-pyrrolidine, and/or polyvinyl alcohol, and tableted or encapsulated for conventional administration.
  • the compounds of this invention may be dissolved in saline, water, polyethylene glycol, propylene glycol, ethanol, corn oil, peanut oil, cottonseed oil, sesame oil, tragacanth gum, and/or various buffers.
  • Other adjuvants and modes of administration are well known in the pharmaceutical art.
  • the carrier or diluent may include time delay material, such as glyceryl monostearate or glyceryl distearate alone or with a wax, or other materials well known in the art.
  • the pharmaceutical compositions may be made up in a solid form (including granules, powders or suppositories) or in a liquid form (e.g., solutions, suspensions, or emulsions).
  • the pharmaceutical compositions may be subjected to conventional pharmaceutical operations such as sterilization and/or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers etc.
  • Solid dosage forms for oral administration may include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound may be admixed with at least one inert diluent such as sucrose, lactose, or starch.
  • Such dosage forms may also comprise, as in normal practice, additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate.
  • additional substances e.g., lubricating agents such as magnesium stearate.
  • the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.
  • Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water. Such compositions may also comprise adjuvants, such as wetting, sweetening, flavoring, and perfuming agents.
  • optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, e.g. , by formation of diastereoisomeric salts, by treatment with an optically active acid or base.
  • appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric, and camphorsulfonic acid and then separation of the mixture of diastereoisomers by crystallization followed by liberation of the optically active bases from these salts.
  • a different process for separation of optical isomers involves the use of a chiral chromatography column optimally chosen to maximize the separation of the enantiomers.
  • Still another available method involves synthesis of covalent diastereoisomeric molecules by reacting compounds of the invention with an optically pure acid in an activated form or an optically pure isocyanate.
  • the synthesized diastereoisomers can be separated by conventional means such as chromatography, distillation, crystallization or sublimation, and then hydrolyzed to deliver the enantiomerically pure compound.
  • the optically active compounds of the invention can likewise be obtained by using active starting materials. These isomers may be in the form of a free acid, a free base, an ester or a salt.
  • the compounds of this invention may exist as isomers, that is compounds of the same molecular formula but in which the atoms, relative to one another, are arranged differently.
  • the alkylene substituents of the compounds of this invention are normally and preferably arranged and inserted into the molecules as indicated in the definitions for each of these groups, being read from left to right.
  • substituents are reversed in orientation relative to the other atoms in the molecule. That is, the substituent to be inserted may be the same as that noted above except that it is inserted into the molecule in the reverse orientation.
  • the compounds of the present invention can be used in the form of salts derived from inorganic or organic acids.
  • the salts include, but are not limited to, the following: acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, cyclopentanepropionate, dodecylsulfate, ethanesulfonate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, fumarate, hydrochloride, hydrobromide, hydroiodide, 2-hyroxy-ethanesulfonate, lactate, maleate, methansulfonate,
  • the basic nitrogen-containing groups can be quatemized with such agents as lower alkyl halides, such as methyl, ethyl, propyl, and butyl chloride, bromides and iodides; dialkyl sulfates like dimethyl, diethyl, dibutyl, and diamyl sulfates, long chain halides such as decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides, aralkyl halides like benzyl and phenethyl bromides, and others. Water or oil-soluble or dispersible products are thereby obtained.
  • lower alkyl halides such as methyl, ethyl, propyl, and butyl chloride, bromides and iodides
  • dialkyl sulfates like dimethyl, diethyl, dibutyl, and diamyl sulfates
  • long chain halides such as de
  • Other examples include salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium or magnesium or with organic bases.
  • pharmaceutically acceptable esters of a carboxylic acid or hydroxyl containing group including a metabolically labile ester or a prodrug form of a compound of this invention.
  • a metabolically labile ester is one which may produce, for example, an increase in blood levels and prolong the efficacy of the corresponding non-esterified form of the compound.
  • a prodrug form is one which is not in an active form of the molecule as administered but which becomes therapeutically active after some in vivo activity or biotransformation, such as metabolism, for example, enzymatic or hydrolytic cleavage.
  • Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl).
  • esters such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl).
  • Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989
  • esters of a compound of this invention may include, for example, the methyl, ethyl, propyl, and butyl esters, as well as other suitable esters formed between an acidic moiety and a hydroxyl containing moiety.
  • Metabolically labile esters may include, for example, methoxymethyl, ethoxymethyl, iso-propoxymethyl, ⁇ -methoxyethyl, groups such as ⁇ -((C ⁇ -C 4 )alkyloxy)ethyl; for example, methoxyethyl, ethoxyethyl, propoxyethyl, iso-propoxyethyl, etc.; 2-oxo-l,3-dioxolen-4-ylmethyl groups, such as 5-methyl-2-oxo-l,3,dioxolen-4-ylmethyl, etc.; C ⁇ -C 3 alkylthiomethyl groups, for example, methylthiomethyl, ethylthiomethyl, isopropylthiomethyl, etc.; acyloxymethyl groups, for example, pivaloyloxymethyl, ⁇ -acetoxymethyl, etc.; ethoxycarbonyl-1 -methyl; or ⁇ -acyloxy- -
  • the compounds of the invention may exist as crystalline solids which can be crystallized from common solvents such as ethanol, N,N-dimethyl-formamide, water, or the like.
  • crystalline forms of the compounds of the invention may exist as solvates and/or hydrates of the parent compounds or their pharmaceutically acceptable salts. All of such forms likewise are to be construed as falling within the scope of the invention.
  • the compounds of the invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more compounds of the invention or other agents.
  • the therapeutic agents can be formulated as separate compositions that are given at the same time or different times, or the therapeutic agents can be given as a single composition.

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Abstract

The compounds of the invention are represented by the following general structure (I) or a pharmaceutically acceptable salt thereof, and compositions containing them, wherein the variables are defined herein, and their use to reduce or inhibit PTH secretion, including methods for reducing or inhibiting PTH secretion and methods for treatment or prophylaxis of diseases associated with bone disorders, such as osteoporosis, or associated with excessive secretion of PTH, such as hyperparathyroidism. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

Description

CALCIUM RECEPTOR MODULATING AGENTS
This application claims the benefit of U.S. Provisional Application No. 60/383,270, filed May 23, 2002, which is hereby incorporated by reference.
Background of the Invention
Extracellular calcium ion concentration is involved in a variety of biological processes, such as blood clotting, nerve and muscle excitability and bone formation (Cell Calcium 11:319, 1990). Calcium ion receptors, which are present on the membranes of various cells in the body, such as parathyroid and kidney cells (Nature 366:574, 1993; J. Bone Miner. Res. 9, Supple. 1, s282, 1994; J. Bone Miner. Res. 9, Supple. 1, s409, 1994; Endocrinology 136:5202, 1995), are important to the regulation of the extracellular calcium ion concentration. For example, concentration of extracellular calcium ion regulates the bone resorption by osteoclasts (Bioscience Reports 10:493, 1990), secretion of parathyroid hormone (PTH) from parathyroid cells and secretion of calcitonin from C-cells (Cell Calcium 11:323, 1990). Parathyroid hormone (PTH) is an important factor in regulating extracellular calcium ion concentration. Secretion of PTH increases extracellular calcium ion concentration by acting on various cells, such as bone and kidney cells, and the extracellular calcium ion concentration reciprocally inhibits the secretion of PTH by acting on parathyroid cells.
Several classes of calcimimetic compounds have been disclosed for regulating extracellular calcium ion concentration, particularly for reducing or inhibiting secretion of PTH. For example, EP 933354; WO 0021910, WO
96/12697; WO 95/11221; WO 94/18959; WO 93/04373; Endocrinology 128:3047, 1991; Biochem. Biophys. Res. commun. 167:807, 1990; J. Bone Miner. Res. 5:581, 1990; and Nemeth et al., "Calcium-binding Proteins in Health and Disease," Academix Press, Inc., pp. 33-35 (1987) disclose various agents which interact with calcium receptors. Dauban et al., Bioorg. Med. Chem. Let. 10:2001-4, 2000, disclose various N 1 -arylsulf onyl-N2-( 1 -aryl)ethyl-3 -phenylpropane- 1 ,2-diamine compounds as calcimimetics acting on the calcium sensing receptor.
Summary of the Invention
The present invention relates to selected calcimimetic compounds and pharmaceutically acceptable salts thereof. The invention compounds advantageously reduce or inhibit PTH secretion. Therefore, this invention also encompasses pharmaceutical compositions, methods for reducing or inhibiting PTH secretion and methods for treatment or prophylaxis of diseases associated with bone disorders, such as osteoporosis, or associated with excessive secretion of PTH, such as hyperparathyroidism. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes. The compounds of the invention are represented by the following general structure
Figure imgf000003_0001
or a pharmaceutically acceptable salt thereof, wherein the variables are defined below. The foregoing merely summarizes certain aspects of the invention and is not intended, nor should it be construed, as limiting the invention in any way. All patents, patent applications and other publications recited herein are hereby incorporated by reference in their entirety.
Detailed Description
The invention provides compounds of Formula (I):
Figure imgf000004_0001
(I) or a pharmaceutically acceptable salt thereof, wherein:
^= represents a double or single bond;
R1 is Rb;
R2 is -salkyl or Cι-4haloalkyl;
R3 is H, Cι-4haloalkyl or Cι-8alkyl;
R4 is H, C^haloalkyl or Cι-8alkyl;
R5 is, independently, in each instance, H, -salkyl, Cι-4haloalkyl, halogen, -OCi-ealkyl, -NRaRd or NRdC(=O)Rd;
X is -CRd=N-, -N=CRd-, O, S or -NRd-; when = is a double bond then Y is =CR - or =N- and Z is -CR = or -N= ; and when — is a single bond then Y is -CRaR6- or -NRd- and Z is -CRaR7- or -NRd-; and
R6 is Rd, Cι-4haloalkyl, -C(=O)Rc, -OC1.6alkyl, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa;
R7 is Rd, C^haloalkyl, -C(=O)Rc, -Od-6alkyl, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa; or R6 and R7 together form a 3- to 6-atom saturated or unsaturated bridge containing 0, 1, 2 or 3 N atoms and 0, 1 or 2 atoms selected from S and O, wherein the bridge is substituted by 0, 1 or 2 substituents selected from R ; wherein when R and R form a benzo bridge, then the benzo bridge may be additionally substituted by a 3- or 4- atoms bridge containing 1 or 2 atoms selected from N and O, wherein the bridge is substituted by 0 or 1 substituents selected from Cι-4alkyl;
Ra is, independently, at each instance, H, Cι- -aloalkyl or Cι-6alkyl; Rb is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from -ealkyl, halogen, C^haloalkyl, -OCι-6alkyl, cyano and nitro;
Rc is, independently, at each instance, Cι-6alkyl, Cι-4haloalkyl, phenyl or benzyl;
Rd is, independently, at each instance, H, Cι-6alkyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the Cι-6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from Cι-6alkyl, halogen, d-4haloalkyl, -OQ-ealkyl, cyano and nitro, R , -C(=O)Rc, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)R°, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; and m is 1 or 2.
In one embodiment, in conjunction with any one of the above and below embodiments, R1 is phenyl substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι-4haloalkyl, -OCι.6alkyl, cyano and nitro.
In another embodiment, in conjunction with any one of the above and below embodiments, R1 is benzyl substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι- haloalkyl, -OCι-6alkyl, cyano and nitro.
In another embodiment, in conjunction with any one of the above and below embodiments, R1 is naphthyl substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, C^haloalkyl, -OCi-6alkyl, cyano and nitro. In another embodiment, in conjunction with any one of the above and below embodiments, R1 is a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 0, 1, 2 or 3 substituents selected from C^alkyl, halogen, Ci.-thaloalkyl, -OCι-6alkyl, cyano and nitro. In another embodiment, in conjunction with any one of the above and below embodiments, R3 and R4 are H.
In another embodiment, in conjunction with any one of the above and below embodiments, R5 is H. In another embodiment, in conjunction with any one of the above and below embodiments, R6 is H.
In another embodiment, in conjunction with any one of the above and below embodiments, R is H.
In another embodiment, in conjunction with any one of the above and below embodiments, X is -NRd-.
In another embodiment, in conjunction with any one of the above and below embodiments:
^^ is a double bond;
Y is =CR6- or =N-; and Z is -CR7= or -N=.
In another embodiment, in conjunction with any one of the above and below embodiments:
==^ is a single bond;
Y is -CRaR6- or -NRd-; and Z is -CRaR7- or -NRd-.
In another embodiment, in conjunction with any one of the above and below embodiments, the invention provides a compound of Formula (II):
Figure imgf000006_0001
(DO wherein:
R >ι1 . is RD;
R >2 i-s Cj-salkyl or C1_4haloalkyl; R3 is H, Cι-4haloalkyl or d.8alkyl;
R4 is H, Ci-4haloalkyl or Cι-8alkyl;
R5 is, independently, in each instance, H, Ci-8alkyl, d-4haloalkyl, halogen, -OCι-6alkyl, -NRaRd or NRdC(=O)Rd; R6 is Rd, d-4haloalkyl, -C(=O)Rc, -OCι-6alkyl, -ORb, -NRaRa, -NRaRb,
-C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa;
R7 is R , Cι- haloalkyl, -C(=O)Rc, -OCι-6alkyl, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa; or R6 and R7 together form a 3- to 6-atom saturated or unsaturated bridge containing 0, 1, 2 or 3 N atoms and 0, 1 or 2 atoms selected from S and O, wherein the bridge is substituted by 0, 1 or 2 substituents selected from R ; wherein when R and R form a benzo bridge, then the benzo bridge may be additionally substituted by a 3- or 4- atoms bridge containing 1 or 2 atoms selected from N and O, wherein the bridge is substituted by 0 or 1 substituents selected from Cι-4alkyl;
Ra is, independently, at each instance, H, Cι-4haloalkyl or d-6alkyl;
Rb is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from d-6alkyl, halogen, Cι-4haloalkyl, -OCι- alkyl, cyano and nitro;
Rc is, independently, at each instance, d-6alkyl, d-4haloalkyl, phenyl or benzyl;
Rd is, independently, at each instance, H, Cι-6alkyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the Cι-6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from d-6alkyl, halogen, d-^aloalkyl, -Od-6alkyl, cyano and nitro, R , -C(=O)Rc, -ORb, ~NRaRa, -NRaR , -C(=O)ORc, -C(=O)NRaRa, -OC(=O)R°, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; and m is 1 or 2.
In another embodiment, in conjunction with any one of the above and below embodiments, the compound has the structure
Figure imgf000008_0001
wherein:
R1 is R ;
R2 is d,8alkyl or d-4haloalkyl; R3 is H, d-4haloalkyl or d-8alkyl;
R4 is H, d-4haloalkyl or Cι-8alkyl;
R5 is, independently, in each instance, H, Cι-8alkyl, d-4haloalkyl, halogen, -OCι.6alkyl, -NRaRd or NRdC(=O)Rd;
R is, independently, at each instance, H, Cι-4haloalkyl or Cι-6alkyl; R is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι-4haloalkyl, -OCι-6alkyl, cyano and nitro;
Rc is, independently, at each instance, Cι-6alkyl,
Figure imgf000008_0002
phenyl or benzyl;
Rd is, independently, at each instance, H, d-6alkyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the Cι_6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from Cι-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro, Rb, -C(=O)Rc, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; and m is 1 or 2.
In another embodiment, in conjunction with any one of the above and below embodiments, R1 is phenyl substituted by 2 or 3 substituents selected from d-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro.
In another embodiment, in conjunction with any one of the above and below embodiments, R1 is benzyl substituted by 1, 2 or 3 substituents selected from d-6alkyl, halogen, Cι-4haloalkyl, -OCι-6alkyl, cyano and nitro.
In another embodiment, in conjunction with any one of the above and below embodiments, R1 is naphthyl substituted by 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι-4haloalkyl, -Od-6alkyl, cyano and nitro. In another embodiment, in conjunction with any one of the above and below embodiments, R1 a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 1, 2 or 3 substituents selected from d-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro.
In another embodiment, in conjunction with any one of the above and below embodiments, one of R3 or R4 is Cι-4haloalkyl or d-8aιkyl.
In another embodiment, in conjunction with any one of the above and below embodiments, R5 is, independently, in each instance, d-8alkyl, d-4haloalkyl, halogen, -Od-6alkyl, -NRaRd or NRdC(=O)Rd.
In another embodiment, in conjunction with any one of the above and below embodiments, R6 is not H.
In another embodiment, in conjunction with any one of the above and below embodiments, R7 is not H. Another aspect of the invention involves a pharmaceutical composition comprising a pharmaceutically acceptable amount of a compound according to any one of Claims 1-22 and a pharmaceutically acceptable diluent or carrier. Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, as a medicament.
Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, in the manufacture of a medicament for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH.
Another aspect of the invention involves the use of a compound in conjunction with any one of the above and below embodiments, in the manufacture of a medicament for the treatment of osteoporosis or hyperparathyroidism.
Another aspect of the invention involves a method of using a compound in conjunction with any one of the above and below embodiments, for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH. Another aspect of the invention involves a method of using a compound in conjunction with any one of the above and below embodiments, for the treatment of osteoporosis or hyperparathyroidism.
Another aspect of the invention involves a process for making a compound in conjunction with any one of the above and below embodiments comprising the step of: reacting a compound having the structure
Figure imgf000010_0001
with an amine having the structure
Figure imgf000010_0002
The compounds may also be synthesized as follows: LiAIH4
Figure imgf000011_0001
, ImH
Figure imgf000011_0003
Figure imgf000011_0002
Bu4NF
Figure imgf000011_0004
In the above reaction scheme, C5H5N.HBr.Br2 is pyridinium hydrobromide perbromide; ImH is imidazole; and DCE is 1,2-dichloroethane
Unless otherwise specified, the following definitions apply to terms found in the specification and claims: "Alkyl" and the prefix "alk" refer to alkyl groups or substituents wherein the carbon atoms are in a branched, cyclical or linear relationship or any combination of the three. "Cv-Walkyl" means an alkyl group comprising from V to W carbon atoms. The alkyl groups described in this section contain from 1 to 10 carbon atoms unless otherwise specified and may also contain a double or triple bond. Examples of d-6 alkyl include, but are not limited to the following:
Figure imgf000011_0005
"Aryl" means a carbocyclic aromatic ring or ring system. Examples of aryl groups include phenyl, naphthyl, indenyl, anthrancenyl, 9-(9-phenylfluorenyl), phenanthrenyl, and the like.
"Halogen" means a halogen atom selected from F, Cl, Br and I. "Haloalkyl", "haloalk-", and "Cv-whaloalkyl" means an alkyl group, as described above, wherein any number— at least one— of the hydrogen atoms attached to the alkyl chain are replaced by F, Cl, Br or I.
"Heterocycle" means a ring comprising at least one carbon atom and at least one other atom selected from N, O and S. Heterocyclic groups can be saturated, unsaturated or aromatic. Aromatic heterocyclic groups are also referred to as "heteroaryl" rings or ring systems. Examples of heterocycles that may be found in the claims include, but are not limited to, the following:
Figure imgf000013_0001
"Pharmaceutically acceptable salt" means a salt prepared by conventional means, and are well known by those skilled in the art. The "pharmaceutically acceptable salts" include basic salts of inorganic and organic acids, including but not limited to hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulphonic acid, ethanesulfonic acid, malic acid, acetic acid, oxalic acid, tartaric acid, citric acid, lactic acid, fumaric acid, succinic acid, maleic acid, salicylic acid, benzoic acid, phenylacetic acid, mandelic acid and the like. When compounds of the invention include an acidic function such as a carboxy group, then suitable pharmaceutically acceptable cation pairs for the carboxy group are well known to those skilled in the art and include alkaline, alkaline earth, ammonium, quaternary ammonium cations and the like. For additional examples of "pharmacologically acceptable salts," see infra and Berge et al., J. Pharm. Sci. 66:1 (1977).
"Leaving group" generally refers to groups readily displaceable by a nucleophile, such as an amine, a thiol or an alcohol nucleophile. Such leaving groups are well known in the art. Examples of such leaving groups include, but are not limited to, N-hydroxysuccinimide, N-hydroxybenzotriazole, halides, triflates, tosylates and the like. Preferred leaving groups are indicated herein where appropriate. "Protecting group" generally refers to groups well known in the art which are used to prevent selected reactive groups, such as carboxy, amino, hydroxy, mercapto and the like, from undergoing undesired reactions, such as nucleophilic, electrophilic, oxidation, reduction and the like. Preferred protecting groups are indicated herein where appropriate. Examples of amino protecting groups include, but are not limited to, aralkyl, substituted aralkyl, cycloalkenylalkyl and substituted cycloalkenyl alkyl, allyl, substituted allyl, acyl, alkoxycarbonyl, aralkoxycarbonyl, silyl and the like. Examples of aralkyl include, but are not limited to, benzyl, ortho- methylbenzyl, trityl and benzhydryl, which can be optionally substituted with halogen, alkyl, alkoxy, hydroxy, nitro, acylamino, acyl and the like, and salts, such as phosphonium and ammonium salts. Examples of cycloalkenylalkyl or substituted cycloalkylenylalkyl radicals, preferably have 6-10 carbon atoms, include, but are not limited to, cyclohexenyl methyl and the like. Suitable acyl, alkoxycarbonyl and aralkoxycarbonyl groups include benzyloxycarbonyl, t- butoxycarbonyl, iso-butoxycarbonyl, benzoyl, substituted benzoyl, butyryl, acetyl, tri-fluoroacetyl, tri-chloro acetyl, phthaloyl and the like. A mixture of protecting groups can be used to protect the same amino group, such as a primary amino group can be protected by both an aralkyl group and an aralkoxycarbonyl group. Amino protecting groups can also form a heterocyclic ring with the nitrogen to which they are attached, for example, l,2-bis(methylene)benzene, phthalimidyl, succinimidyl, maleimidyl and the like and where these heterocyclic groups can further include adjoining aryl and cycloalkyl rings. In addition, the heterocyclic groups can be mono-, di- or tri-substituted, such as nitrophthalimidyl. Amino groups may also be protected against undesired reactions, such as oxidation, through the formation of an addition salt, such as hydrochloride, toluenesulfonic acid, trifluoroacetic acid and the like. Many of the amino protecting groups are also suitable for protecting carboxy, hydroxy and mercapto groups. For example, aralkyl groups. Alkyl groups are also suitable groups for protecting hydroxy and mercapto groups, such as tert- butyl.
Silyl protecting groups are silicon atoms optionally substituted by one or more alkyl, aryl and aralkyl groups. Suitable silyl protecting groups include, but are not limited to, trimethylsilyl, triethylsilyl, tri-isopropylsilyl, tert- butyldimethylsilyl, dimethylphenylsilyl, 1 ,2-bis(dimethylsilyl)benzene, l,2-bis(dimethylsilyl)ethane and diphenylmethylsilyl. Silylation of an amino groups provide mono- or di-silylamino groups. Silylation of aminoalcohol compounds can lead to a N,N,O-tri-silyl derivative. Removal of the silyl function from a silyl ether function is readily accomplished by treatment with, for example, a metal hydroxide or ammonium fluoride reagent, either as a discrete reaction step or in situ during a reaction with the alcohol group. Suitable silylating agents are, for example, trimethylsilyl chloride, tert-butyl-dimethylsilyl chloride, phenyldimethylsilyl chloride, diphenylmethyl silyl chloride or their combination products with imidazole or DMF. Methods for silylation of amines and removal of silyl protecting groups are well known to those skilled in the art. Methods of preparation of these amine derivatives from corresponding amino acids, amino acid amides or amino acid esters are also well known to those skilled in the art of organic chemistry including amino acid/amino acid ester or aminoalcohol chemistry.
Protecting groups are removed under conditions which will not affect the remaining portion of the molecule. These methods are well known in the art and include acid hydrolysis, hydrogenolysis and the like. A preferred method involves removal of a protecting group, such as removal of a benzyloxycarbonyl group by hydrogenolysis utilizing palladium on carbon in a suitable solvent system such as an alcohol, acetic acid, and the like or mixtures thereof. A t- butoxycarbonyl protecting group can be removed utilizing an inorganic or organic acid, such as HC1 or trifluoroacetic acid, in a suitable solvent system, such as dioxane or methylene chloride. The resulting amino salt can readily be neutralized to yield the free amine. Carboxy protecting group, such as methyl, ethyl, benzyl, tert-butyl, 4-methoxyρhenylmethyl and the like, can be removed under hydrolysis and hydrogenolysis conditions well known to those skilled in the art.
It should be noted that compounds of the invention may contain groups that may exist in tautomeric forms, such as cyclic and acyclic amidine and guanidine groups, heteroatom substituted heteroaryl groups (Y' = O, S, NR), and the like, which are illustrated in the following examples:
Figure imgf000016_0001
and though one form is named, described, displayed and/or claimed herein, all the tautomeric forms are intended to be inherently included in such name, description, display and/or claim.
Prodrugs of the compounds of this invention are also contemplated by this invention. A prodrug is an active or inactive compound that is modified chemically through in vivo physiological action, such as hydrolysis, metabolism and the like, into a compound of this invention following administration of the prodrug to a patient. The suitability and techniques involved in making and using prodrugs are well known by those skilled in the art. For a general discussion of prodrugs involving esters see Svensson and Tunek Drug Metabolism Reviews 165 (1988) and Bundgaard Design of Prodrugs, Elsevier (1985). Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl).
Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989)). Also, drugs containing an acidic NH group, such as imidazole, imide, indole and the like, have been masked with N- acyloxymethyl groups (Bundgaard Design of Prodrugs, Elsevier (1985)).
Hydroxy groups have been masked as esters and ethers. EP 039,051 (Sloan and
Little, 4/11/81) discloses Mannich-base hydroxamic acid prodrugs, their preparation and use.
Preferred compounds of the invention include:
(R)-N-( 1 -( 1 -Νaphthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-( 1 -( 1 -Νaphthyl)ethyl)-N-(2' -ethyl-benzotriazol-5-ylmethyl)amine; (R)-N-(l-((Phenyl)ethyl)-N-((l-ethylcyclopent[b]indol-5-yl)methyl)amine;
(R)-N-(l-(l-Νaphthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-(l-(Phenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-(l-((l-naphthyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[4,3-b]indole-8- yl)methyl)amine;
( lR)-Ν-(( 1 -ethyl-3 -phenyl- lΗ-indol-5-yl)methyl)- 1 -phenylethanamine;
(lR)-N-((l-ethyl-3-(3-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine ;
(lR)-N-((l-ethyl-3-(3-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l-l- naphthalenyl)ethanamine;
(lR)-N-((l-ethyl-3-(3-(trifIuoromethyl)phenyl)-lH-indol-5-yl)methyl)-l- (3-
(methyloxy)phenyl)ethanamine;
(lR)-l-(3-(methyloxy)phenyl)-N-((l-(4-(trifluoromethyl)phenyl)-lH-indol-5- yl)methyl)ethanamine; and pharmaceutically acceptable salts thereof. Experimental GENERAL METHODS
In the following synthetic methods references to "the aldehyde" and "the amine" refer to the reaction of an aldehyde of the following formula:
Figure imgf000018_0001
with an amine having the structure
Figure imgf000018_0002
Method A The aldehyde (1.6 mmol) is dissolved in methanol (5 mL) and the amine (1.9 mmol) is added. The reaction is shaken for 24 hours or until imine formation is complete (as monitored by LCMS), then solid-supported borohydride is added (prepared according to Kabalka, G. W.; Wadgaonkar, P. P.; Chatla, N.; Synth. Commun.; (1990), 20 (2), 293-299) (ca 2.5 mmol/g; 3.1 mmol) and the mixture is shaken for 24 hours or until reduction is complete (as monitored by LCMS). Dichloromethane (ca 3 mL) is then added followed by Wang-aldehyde resin (4-benzyloxybenzaldehyde, polymer-bound; ca 1.25mmol/g; 0.6 mmol) and the mixture is shaken for further 24 hours. The resins are filtered off and the solvents are evaporated under reduced pressure, to afford an oil which is purified by column chromatography (usually Hexane/AcOEt 7/3 or DCM/MeOH 95/5). The free-base oil is then treated with 1.5-2.5 mL IN HCl in diethyl ether and the solvents are evaporated under reduced pressure to afford the mono or bis-HCl salt.
Method B The aldehyde (1.6 mmol) is dissolved in methanol (5 mL) and the amine (1.9 mmol) is added. The reaction is heated to reflux for 10 minutes then left to cool overnight until imine formation is complete (as monitored by LCMS). Solid-supported cyanoborohydride is added (prepared according to Sande, A. R.; Jagadale, M. H.; Mane, R. B.; Salunkhe, M. M.; Tetrahedron Lett. (1984), 25(32), 3501-4) (ca 2.5mmol/g; 3.1 mmol) and the mixture is heated at 50 °C for 15 hours or until reduction is complete (as monitored by LCMS). Dichloromethane (ca 3 mL) is then added followed by Wang-aldehyde resin (4- benzyloxybenzaldehyde, polymer-bound; ca 1.25 mmol/g; 0.6 mmol) and the mixture is shaken for further 24 hours. The resins are filtered off and the solvents are evaporated under reduced pressure, to afford an oil which is purified by column chromatography (usually Hexane/AcOEt 7/3 or DCM/MeOH 95/5). The free-base oil is then treated with 1.5-2.5 mL IN HCl in diethyl ether and the solvents are evaporated under reduced pressure to afford the mono or bw-HCl salt.
Method C The aldehyde (1.6 mmol) is dissolved in 1,2-dichloroethane (12 mL) and the amine (1.9 mmol) is added, followed by acetic acid (0.09 mL, 1.6 mmol) and finally sodium triacetoxyborohydride (500 mg, 2.4 mmol). The mixture is stirred overnight or until complete by TLC. Upon reaction completion, the mixture is diluted with ethyl acetate, washed with saturated NaHCO3, then with saturated brine, and finally dried over sodium sulfate. The solvents are evaporated under reduced pressure, to afford an oil which is purified by column chromatography on silica gel (usually Hexane/ AcOEt 7/3 or DCM/MeOH 95/5). The free-base oil is then treated with 1.5-2.5 IN HCl in diethyl ether and the solvents are evaporated under reduced pressure to afford the mono or bw-HCl salt.
Example 1
(R)-N-( 1 -( 1 -Νaphthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine
Figure imgf000019_0001
The title compound was prepared by the method C.
C27H26 N2O Mass (calculated): [378]; (found): [M+H1"] = 379
NMR (400 MHz, CDC13): 1.5 (3H, t, 7=7 Hz, CH3CH2); 1.65 (3H, d, J=7 Hz,
NCHCH3); 3.9 and 4.0 (2H, dd, 7=14 Hz, CH2N); 4.4 (2H, q, 7=7 Hz, CH3CH2);
4.85 (IH, q, 7=7 Hz, NCHMe); 7.25 (IH, t, 7=7 Hz, aryl-H); 7.35-7.55 (6H, m, aryl-H); 7.6 (IH, t, 7=7 Hz, aryl-H); 7.85 (IH, d, 7=7 Hz); 7.9-8 (2H, m, aryl-H);
8 (IH, s, aryl-H); 8.05 (IH, d, 7=7 Hz, aryl-H); 8.2 (IH, bd, 7=7 Hz; aryl-H).
Example 2
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine
Figure imgf000020_0001
The title compound was prepared by the method C.
C24H26 Ν2O Mass (calculated): [358]; (found): [M+H1"] = 359.
NMR (400 MHz, CDC13): 1.3-1.4 (6H, m, NCHCH3 and CH2CH3); 3.7 (IH, d, 7=
12 Hz, CH2N); 3.75-3.83 (5H, m, CH2N, CHCH3, OCH3); 4.3 (2H, q, 7= 7 Hz,
CH2CH3); 6.75 (IH, m, aryl-H); 6.9 (2H, m, aryl-H); 7.1-7.42 (6H, m, aryl-H); 7.9
(IH, s, aryl-H); 8.0 (IH, d, 7= 7 Hz, aryl-H).
Example 3
(R)-N-(l-(l-Naphthyl)ethyl)-N-(l-ethyl-5-indolylmethyl)amine
Figure imgf000021_0001
The title compound was prepared by the method C.
C23H2 N2 Mass (calculated): [328]; (found): [M+H1"] = 329, 157.
NMR (400 MHz, CDC13): 1.29 (3H, t, 7= 7.6 Hz, CH2CH3); 1.39 (3H, d, 7= 6.6
Hz; CHCH3); 3.67 and 3.76 (2H, dd, 7= 12.7 Hz, CH2N); 4.0 (2H, q, 7= 7.6 Hz,
CH2CH3); 4.6 (IH, q, 7= 6.6 Hz, CHCH3); 6.32 (IH, d, 7= 3 Hz, indole-H); 6.95
(IH, d, 7= 3 Hz, indole-H); 7.05 (IH, dd, 7= 1.5 and 8 Hz, aryl-H); 7.16 (IH, d,
7= 8.6 Hz, aryl-H); 7.3-7.5 (3H, m, aryl-H); 7.63 (IH, d, 7= 7.6 Hz, aryl-H); 7.7-
7.8 (2H, m, aryl-H); 8.0-8.1 (IH, m, aryl-H).
Example 4
Figure imgf000021_0002
Example 4A: Ethyl 2-ethylbenzotriazole-5-carboxylate Benzotriazole-5-carboxylic acid (1.5 g, 9.2 mmol) and ethyl iodide (1.61 mL, 20.2 mmol) were dissolved in DMF (20 mL and sodium hydride (0.800 g, 20.2 mmol, 60% suspension in mineral oil) was added. The mixture was stirred under nitrogen at 55 °C for one hour then the reaction was cooled and quenched with water, diluted with ethyl acetate and washed with water. The organic phase was separated and dried over sodium sulfate. The crude was purified by column chromatography (ethyl acetate/hexane 3/2 and the major isomer isolated (0.76 g) was tentatively assigned as the title compound (cfr also Palmer, M.H., Findlay, R. H. et al. . J.Chem. Soc. PerkinTrans. 2, 1975, 1695-1700). C11H13N3O2 Mass (calculated): [219]; (found): [M+H1"] = 220. NMR (400 MHz, CDC13): 1.3 (3H, t, 7 = 7 Hz, CH2CH3); 1.6 (3H, t, 7 = 7 Hz, CH2CH3); 4.3 (2H, q, 7 = 7 Hz, CH2CH3); 4.7 (2H, q, 7 = 7 Hz, CH2CH3); 7.8 (IH, d, 7= 8.5 Hz, aryl-H); 7.95 (IH, d, 7 = 8.5 Hz, aryl-H); 8.6 (IH, s, aryl-H).
Example 4B: 2-Ethyl-5-hydroxymethylbenzotriazole
Ethyl 2-etliylbenzotriazole-5-carboxylate (0.7g, 3.06 mmol) was dissolved in dry toluene (10 mL) and cooled to 0 °C under nitrogen. A solution of DIBAL-H (1.5M in toluene, 3 mL, 4.5 mmol) was then added dropwise to the cooled solution over 15 minutes. The reaction was stirred at 0 °C for one hour when further DIBAL-H (1.5 mL, 2.25 mmol) was added. A further aliquot of DIBAL-H (0.75 mL, 1.12 mmol) was added after 2 hours and the reaction was stirred for further 30 min. The reaction was quenched by addition of a saturated solution of sodium potassium tartrate, diluted with water and extracted with AcOEt. The organic layer was dried over sodium sulfate to give a crude oil (440 mg) which was used directly in the following step. C9HπN3O Mass (calculated): [177]; (found): [M+H"] = 178 NMR (400 MHz, CDC13): 1.6 (3H, t, 7 = 7 Hz, CH2CH3); 4.65 (2H, q, 7 = 7 Hz, CH2CH3); 4.75 (2H, s, CH2O); 7.25 (IH, dd, 7= 8.5 and 2 Hz, aryl-H); 7.7-7.75 (IH, m, aryl-H); 7.75 (IH, s, aryl-H).
Example 4C: 2-Ethyl-5-formylbenzotriazole. The crude alcohol from the previous step (440 mg, 2.49 mmol) was dissolved in acetone (10 mL) and treated with manganese dioxide (2.6 g, 29.9 mmol). The reaction was stirred at room temperature for 72 hours then the solid filtered off to afford the aldehyde which was used without further purification C9H9N3O Mass (calculated): [175]; (found): [M+H*] = 176 NMR (400 MHz, CDC13): 1.6 (3H, t, 7 = 7 Hz, CH2CH3); 4.75 (2H, q, 7 = 7 Hz,
CH2CH3); 7.8-7.85 (2H, m, aryl-H); 8.2 (IH, s, aryl-H); 9.8 (IH, s, CHO) Example 4D: (R)-N-(l-(l-Naphthyl)ethyl)-N-(2'-ethyl-benzotriazol-5- ylmethyl)amine
Prepared according to General Procedure C. C21H22Ν4 Mass (calculated): [330]; (found): [M+H1"] = 155, 331. NMR (400 MHz, CDC13): 1.45 (3H, d, 7 = 7 Hz, CH3CHN); 1.65 (3H, t, 7 = 7 Hz, CH3CH2N); 3.75 and 3.8 (2H, dd, 7 = 12 Hz, aryl-CH2N); 4.6-4.7 (3H, m, aryl- CHCH3 and CH2CH3); 7.25 (IH, dd, 7= 8.5 and 2 Hz, aryl-H); 7.35-7.4 (3H, m, aryl-H); 7.7-7.75 (4H, m, aryl-H); 7.75-7.8 (IH, m, aryl-H); 8.05-8.1 (IH, m, aiyl- H).
Example 5
Figure imgf000023_0001
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(2'-ethyl-benzotriazol-5-ylmethyl)amine Prepared according to General Procedure C. C18H22Ν4O Mass (calculated): [310]; (found): [M+H^] = 311.
NMR (400 MHz, CDC13): 1.3 (3H, d, 7= 7 Hz, CH3CHN); 1.65 (3H, t, 7= 7 Hz, CH3CH2N); 3.6-3.85 (6H, m, CH3O, aryl-CHCH3 and aryl-CH2N) ; 4.65-4.75 (2H, m, CH2CH3); 7.7-6.75 (IH, m, aryl-H); 6.85-6.9 (2H, m, aryl-H); 7.15-7.25 (IH, m, aryl-H); 7.25-7.3 (IH, m, aryl-H); 7.65 (IH, s, aryl-H); 7.75-7.8 (IH, m, aryl-H).
Example 6
Figure imgf000024_0001
(R)-N-( 1 -(Phenyl)ethyl)-N-(2' -ethyl-benzotriazol-5-ylmethyl)amine
Prepared according to General Procedure C.
Cι7H20Ν4 Mass (calculated): [280]; (found): [M+H+] = 281.
NMR (400 MHz, CDC13): 1.3 (3H, d, 7= 7 Hz, CH3CHN); 1.65 (3H, t, 7= 7 Hz,
CH3CH2N); 3.6 and 3.7 (2H, dd, 7= 12 Hz, aryl-CH2N) ; 3.75 (IH, q, 7= 7 Hz,
NCHCH3); 4.7 (2H, q, 7= 7 Hz, CH2CH3); 7.15-7.2 (IH, m, aryl-H); 7.20-7.30
(5H, m, aryl-H); 7.65 (IH, s, aryl-H); 7.7 (IH, d, 7 = 8 Hz, aryl-H).
Figure imgf000024_0002
Example 7A: 6-Methoxy-l,2,3,4-tetrahydrocarbazole-3-carboxylic acid ethyl ester.
A solution of ethyl 4-oxocyclohexanecarboxylate (3 g, 17.6 mmol) and sodium acetate (1.59 g, 19.4 mmol) in glacial acetic acid (36 mL) was degassed with nitrogen prior to addition of 4-methoxyphenylhydrazine hydrochloride (3.38 g, 19.4 mmol). The mixture was heated at reflux for 2 hours then cooled, poured into water and extracted with tert-butylmethyl ether. The organic phase was washed with 5% K2CO3, then water and finally brine. The organic layer was dried over sodium sulphate then solvent removed under reduced pressure and the residue purified by column chromatography to afford 3.29 g of the title compound. C16H19NO3 Mass (calculated): [273]; (found): [M+H1"] = 274. NMR (400 MHz, CDC13): 1.22 (3H, t, 7= 6 Hz, CH3CH2O); 1.85-2.0 (IH, m, cyclohexenyl-H); 2.2-2.3 (IH, m, cyclohexenyl-H); 2.65-2.85 (4H, m, cyclohexenyl-H); 2.9-3.0 (IH, m, cyclohexenyl-H); 3.75 (3H, s, CH3O); 4.15 (2H, q, 7 = 6 Hz, OCH2CH3); 6.7 (IH, dd, 7 = 2 and 8 Hz, aryl-H); 6.85 (IH, d, 7 = 2 Hz, aryl-H); 7.1 (IH, d, 7 = 8 Hz, aryl-H); 7.55 (IH, bs, NH).
Example 7B: 6-Methoxycarbazole-3-carboxylic acid ethyl ester.
A solution of 6-methoxy-l,2,3,4-tetrahydrocarbazole-3-carboxylic acid ethyl ester (3.29 g, 12.1 mmol) in p-cymene (12 mL) was treated with palladium (10% on carbon, 2.25 g) and heated at 190 °C for 20 hours. The mixture was then cooled, diluted with dichloromethane and filtered over a pad of diatomaceous earth. The filtrate was concentrated in vacuo to a low volume and heptane (200 mL) was added to precipitate the title compound as a white solid (2.78 g). C16Hι5NO3 Mass (calculated): [269]; (found): [M+H+] = 270. NMR (400 MHz, CDC13): 1.4 (3H, t, 7= 6 Hz, CH3CH2O); 3.85 (3H, s, CH3O);
4.4 (2H, q, 7= 6 Hz, OCH2CH3); 7.0 (IH, dd, 7= 2 and 8 Hz, aryl-H); 7.3 (IH, d, 7 = 8 Hz, aryl-H); 7.35 (IH, d, 7 = 8 Hz, aryl-H); 7.55 (IH, d, 7 = 2 Hz, aryl-H);
8.05 (IH, dd, 7= 1 and 8 Hz); 8.15 (IH, bs, NH); 8.7 (IH, d, 7= 1 Hz, aryl-H).
Example 7C: 9-Ethyl-6-methoxycarbazole-3-carboxylic acid ethyl ester
A solution of 6-methoxycarbazole-3-carboxylic acid ethyl ester (1.28 g, 4.77 mmol) in DMF (8 mL) was added to a suspension of sodium hydride (60% in mineral oil, 0.286 mg, 7.15 mmol) in DMF at 0 °C. The reaction was stirred for 30 minutes then ethyl iodide was added (0.89 g, 5.72 mmol). The reaction was allowed to reach room temperature and was stirred for further 15 hours then was diluted with NH CI sat. and water. The reaction was extracted with tert- butylmethyl ether and the organic phase was washed with water then brine. The organic layer was dried over sodium sulfate and the solvent concentrated in vacuo to give a crude which was purified by column (10% ethyl acetate/hexane) to afford 0.79 g of the title compound.
Ci8H19NO3 Mass (calculated): [297]; (found): [M+H*] = 298. NMR (400 MHz, CDC13): 1.35-1.45 (6H, m, CH3CH2O and CH3CH2N ); 3.9 (3H, s, CH3O); 4.3 (2H, q, 7 = 6 Hz, NCH2CH3); 4.4 (2H, q, 7 = 6 Hz, OCH2CH3); 7.1 (IH, dd, 7 = 2 and 8 Hz, aryl-H); 7.32 (IH, d, 7 = 8 Hz, aryl-H); 7.35 (IH, d, 7 = 8 Hz, aryl-H); 7.55 (IH, d, 7= 2 Hz, aryl-H); 8.1 (IH, dd, 7= 1 and 8 Hz); 8.15 (IH, bs, NH); 8.7 (IH, d, 7= 1 Hz, aryl-H).
Example 7D: 9-Ethyl-3-hydroxymethyl-6-methoxycarbazole
A solution of 9-ethyl-6-methoxycarbazole-3-carboxylic acid ethyl ester (1.36 g, 4.58 mmol) in anhydrous THF was added to a solution of lithium aluminum hydride in THF (25 mL) at 0 °C. The reaction was stirred for 1 hour then water (1 mL) was added followed by 2M NaOH (1 mL) and finally water (1 mL). The reaction was then filtered on diatomaceous earth and the filtrate was dried and solvent removed in vacuo to afford 0.79 g of the crude alcohol. Cι6Hι7NO2 Mass (calculated): [255]; (found): [M+H"1"] = 238, 255.
Example 7E: 9-Ethyl-6-methoxycarbazole-3-carboxaldehyde A solution of 9-ethyl-3-hydroxymethyl-6-methoxycarbazole (0.305 g, 1.2 mmol) in acetone (5 mL) was treated with MnO2 (0.52 g, 6 mmol) and the reaction stirred at room temperature for 60 hours. The reaction mixture was filtered and the solvent evaporated under reduced pressure. The crude was purified by column chromatography (heptane/ethyl acetate 5/1) to afford 0.190 mg of the title compound.
Cι8H19NO3 Mass (calculated): [253]; (found): [M+H1"] = 254 NMR (400 MHz, CDC13): 1.3 (3H, t, 7 = 6 Hz, CH3CH2N ); 3.85 (3H, s, CH3O); 7.1 (IH, dd, 7 = 2 and 8 Hz, aryl-H); 7.3 (IH, d, 7 = 8 Hz, aryl-H); 7.35 (IH, d, 7 = 8 Hz, aryl-H); 7.55 (IH, d, 7= 2 Hz, aryl-H); 7.9 (IH, dd, 7= 1 and 8 Hz); 8.4 (IH, d, 7 = 1 Hz, aryl-H); 10 (IH, s, CHO). Example 7F: (R)-N-(l-(l-Naphthyl)ethyl)-N-(9-ethyl-6-methoxy-3- carbazolylmethyl)amine Prepared according to general procedure C. C28H28Ν2O Mass (calculated): [408]; (found): [M+H1"] = 238, 409. NMR (400 MHz, CDC13): 1.3 (3H, t, 7 = 6 Hz, CH3CH2N ); 1.45 (3H, d, 7 = 6 Hz, CH3CHN); 3.8 (IH, d, 7= 12 Hz, aryl-CH2N); 3.85 (3H, s, CH3O); 3.9 (IH, d, 7 = 12 Hz, aryl-CH2N); 4.25 (IH, q, 7 = 6 Hz, NCH2CH3); 4.7 (IH, q, 7 = 6 Hz, CH3CHN); (7.1 (IH, dd, 7= 2 and 8 Hz, aryl-H); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.35 (IH, d, 7 = 8 Hz, aryl-H); 7.4-7.45 (IH, m, aryl-H); 7.5-7.55 (3H, m, aryl-H); 7.7 (IH, d, 7 = 8 Hz, aryl-H); 7.75 (IH, d, 7 = 8 Hz, aryl-H); 7.8-7.9 (2H, m, aryl- H); 8-8.1 (lH, m, aryl-H).
Figure imgf000027_0001
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-6-methoxy-3-carbazolylmethyl)- amine
Prepared according to general procedure C.
C25H28Ν2O2 Mass (calculated): [388]; (found): [M+H ] = 238, 389, 777.
NMR (400 MHz, CDC13): 1.3-1.4 (6H, m, CH3CH2N and CH3CHN); 3.7 (IH, d, 7 = 12 Hz, aryl-CH2N); 3.75-3.85 (5H, m, CH3O, aryl-CH2N, CH3CHN); 4.25 (IH, q, 7= 6 Hz, NCH2CH3); 6.85 (IH, dd, 7= 2 and 8 Hz, aryl-H); 6.9-6.95 (2H, m, aryl-H); 7.1 (IH, dd, 7 = 2 and 8 Hz, aryl-H); 7.25-7.35 (4H, m, aryl-H); 7.5 (IH, d, 7= 2 Hz, aryl-H); 7.9 (IH, s, aryl-H). Example 9
Figure imgf000028_0001
(R)-N-(l-((Phenyl)ethyl)-N-(9-ethyl-6-methoxy-3-carbazolylmethyl)amine Prepared according to general procedure C.
CΛeΝzO Mass (calculated): [358]; (found): [M+H""] = 238, 359. ΝMR (400 MHz, CDC13): 1.3-1.35 (6H, m, CH3CH2Ν and CH3CHN); 3.7 (IH, d, 7= 12 Hz, aryl-CH2N); 3.75 (7 (IH, d, 7 = 12 Hz, aryl-CH2N); 3.8 (IH, q, 7= 6 Hz, CH3CHN); 3.85 (3H, s, CH3O); 4.25 (IH, q, 7= 6 Hz, NCH2CH3); 7.1 (IH, dd, 7 = 2 and 8 Hz, aryl-H); 7.25-7.4 (8H, m, aryl-H); 7.5 (IH, d, 7 = 2 Hz, aryl- H); 7.9 (IH, s, aryl-H)
Example 10
Figure imgf000028_0002
(R)-N-(l-((Phenyl)ethyl)-N-((l-ethylcyclopent[b]indol-5-yl)methyl)amine.
Example 10A: 5-Cyanocyclopent[b]indole
A solution of cyclopentanone (1 g, 12.0 mmol), 4-cyanophenylhydrazine hydrochloride (2.2 g, 13.1 mmol) and sodium acetate (1.07 g, 13 mmol) in glacial acetic acid (20 mL) was refluxed 2 hours then cooled and poured into water and extracted with dichloromethane. The organic layer was washed with NaHCO3 sat. and water, then dried over sodium sulfate and solvent removed in vacuo. The crude was purified by column chromatography (40/60 ethyl acetate/hexane) to give 980 mg of title compound.
C12H12N2 Mass (calculated): [182]; (found): [M+H*] = 183.
NMR (400 MHz, CDC13): 2.45-2.55 (2H, m, cyclopentyl-H); 2.75-2.85 (4H, m, cyclopentyl-H); 7.3 (2H, s, aryl-H); 7.8 (IH, s, aryl-H); 8.1 (IH, bs, NH).
Example 10B: 5-Cyano-l-ethylcyclopent[b]indole
A solution of 7-cyano- 1,2,3, 4-tetrahydrocyclopent[b]indole (0.224 g, 1.23 mmol) in anhydrous DMF (15 mL) was cooled to 0 °C and sodium hydride (60% dispersion in mineral oil, 74 mg, 3.07 mmol) was added. The reaction was stirred for 45 minutes then ethyl iodide (0.171 g, 1.47 mmol) was added and the reaction was allowed to warm to room temperature. The mixture was stirred for 15 hours then water was added. The product precipitated and was collected by filtration, washing with little water, brine and dichloromethane to give 0.287 g of title compound. Ci4Hi4N2 Mass (calculated): [210]; (found): [M+H1"] = 211. NMR (400 MHz, CDC13): 1.3 (3H, t, 7 = 2 Hz, CH3CH2N); 2.45-2.6 (2H, m, cyclopentyl-H); 2.75-2.9 (4H, m, cyclopentyl-H); 4.1 (IH, q, 7= 6 Hz, NCH2CH3); 7.2-7.3 (2H, m, aryl-H); 7.7 (IH, s, aryl-H)
Example 10C: l-ethylcyclopent[b]indole-5-carboxaldehyde A solution of 7-cyano-4-ethyl-l,2,3,4-tetrahydrocyclopent[b]indole (0.28 g, 1.33 mmol) in dichloromethane (15 mL) was cooled in an ice-bath then treated with DIBAL-H (0.189 g, 1.33 mmol). The reaction was then allowed to reach room temperature and was stirred for 15 hours before diluting with dichloromethane and pouring into a saturated solution of sodium potassium tartrate. The organic layer was separated then washed with brine. The crude product was purified by column chromatography eluting with dichloromethane, to afford 0.2 g of title compound. C14Hι5NO Mass (calculated): [213]; (found): [M+H1"] = 214 NMR (400 MHz, CDC13): 1.3 (3H, t, 7 = 2 Hz, CH3CH2N); 2.45-2.55 (2H, m, cyclopentyl-H); 2.75-2.85 (4H, m, cyclopentyl-H); 4.1 (IH, q, 7= 6 Hz, NCH2CH3); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.75 (IH, dd, 7= 1 and 8 Hz, aryl-H), 7.9 (IH, d, 7 = 1 Hz, aryl-H); 9.7 (IH, s, CHO)
Example 10D: (R)-N-(l-((Phenyl)ethyl)-N-((l-ethylcyclopent[b]indol-5- yl)methyl)amine
Prepared according to general procedure C. C22H26Ν2 Mass (calculated): [318]; (found): [M+H ] = 198, 319.
NMR (400 MHz, CDC13): 1.2-1.3 (6H, m, (6H, m, CH3CH2N and CH3CHN); 2.4- 2.5 (2H, m, cyclopentyl-H); 2.75-2.85 (4H, m, cyclopentyl-H); 3.55 (IH, d, 7 = 12 Hz, aryl-CH2N); 3.65 (IH, d, 7= 12 Hz, aryl-CH2N); 3.75 (IH, 2, (IH, d, 7= 6 Hz, CH3CHN); 3.95 (2H, q, NCH2CH3); 6.9 (IH, dd, (IH, d, 7= 2 and 8 Hz, aryl-H); 7.1 (IH, d, (IH, d, 7= 8 Hz, aryl-H); 7.2-7.3 (IH, m, aryl-H); 7.3-7.4 (5H, m, aryl-H) .
Example 11
Figure imgf000030_0001
(R)-N-(l-(l-Naphthyl)ethyl)-N-((l-methylbenzimidazol-5-yl)methyl)amine
Example 11 A: Methyl l-methylbenzimidazole-5-carboxylate A solution of methyl 3-amino-4-methylaminobenzoate (prepared as in DE 1990390463 Al) (2.57 g, 14 mmol) in trimethyl orthoformate (50 mL) was refluxed for 16 hours. The solvent was then removed under reduced pressure to afford 2.31 g of product. CιoHι0Ν2O2 Mass (calculated): [190]; (found): [M+H÷] = 191. NMR (400 MHz, dmso-d6): 3.95 (3H, s, NCH3); 4.0 (3H, s, OCH3); 7.8 (IH, d, 7 = 8 Hz, aryl-H); 8.0 (IH, dd, 7 = 1 and 8 Hz, aryl-H); 8.35 (IH, d, 7 = 1 Hz, aryl- H); 8.45 (IH, s, imidazole-H).
Example 1 IB: 5-Hydroxymethyl-l-methylbenzimidazole
A solution of methyl l-methylbenzimidazole-5-carboxylate (1.6 g, 8.42 mmol) in dry THF (80 mL) was treated with LiAlH (1.59 g, 42.1 mmol) and the mixture stirred for 2 hours. 1.5 mL of 5% NaOH solution was then added, and the solid which precipitated was filtered through diatomaceous earth. The filtrate was collected and the solvent removed under reduced pressure to give 0.8 g of the title compound.
C9H10N2O NMR (400 MHz, DMSO-d6): 3.85 (3H, s, NCH3); 4.65 (2H, s, CH2OH); 5.25 (IH, bs, OH); 7.3 (IH, dd, 7 = 1 and 8 Hz, aryl-H); 7.55 (IH, d, 7 = 8 Hz, aryl-H); 7.65 (IH, d, 7= 1 Hz, aryl-H); 8.2 (IH, s, imidazole-H)
Example 11C: l-Methylbenzimidazole-5-carboxaldehyde A solution of 5-hydroxymethyl-l-methylbenzimidazole (0.8 g, 4 mmol) in acetone (40 mL) was treated with MnO2 (4 g) and the mixture was stirred for 3 days. The solid was filtered off and the solvent removed under reduced pressure to give 0.63 g of product.
C9H8N2O Mass (calculated): [160]; (found): [M+H"1"] = 161. NMR (400 MHz, dmso-d6): 3.95 (3H, s, NCH3); 7.8 (IH, d, 7= 8 Hz, aryl-H); 7.9 (IH, dd, 7 = 1 and 8 Hz, aryl-H); 8.3 (IH, d, 7= 1 Hz, aryl-H); 8.45 (IH, s, imidazole-H); 10.1 (IH, s, CHO).
Example 1 ID: (R)-N-(l-(l-naphthyl)ethyl)-N-((l-methylbenzimidazol-5- yl)methyl)amine
Prepared according to general procedure C.
C2ιH2ιΝ3 Mass (calculated): [315]; (found): [M+H*] = 316, 155, 631. NMR (400 MHz, CDC13): 1.55 (3H, d, 7 = 7 Hz, CH3CHN); 3.7-3.8 (4H, m, imidazole NCH3 and aryl-CH2N); 3.95 (IH, d, 7= 11 Hz, aryl-CH2N); 4.05 (IH, q, 7= 7 Hz, NCHCH3); 7.25-7.35 (2H, m, aryl-H); 7.45-7.55 (3H, m, aryl-H); 7.75-7.85 (3H, m, aryl-H); 7.85-7.95 (2H, m, aryl-H); 8.15-8.25 (IH, m, aryl-H).
Example 12
Figure imgf000032_0001
(R)-N-(l-(Phenyl)ethyl)-N-((l-methylbenzimidazol-5-yl)methyl)amine Prepared according to general procedure C. Cι7Hι Ν3
Mass (calculated): [265]; (found): [M+H4] = 266, 531. NMR (400 MHz, CDC13): 1.3 (3H, d, 7= 7 Hz, CH3CHN); 3.65 (IH, d, 7= 11
Hz, aryl-CH2N); 3.7-3.8 (5H, m, imidazole NCH3, CH3CHN and aryl-CH2N); 7.1- 7.3 (7H, m, aryl-H); 7.6 (IH, s, aryl-H); 7.8 (IH, s, aryl-H).
Example 13
Figure imgf000032_0002
(R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-2-methyl-l,2,5,6-tetrahydropyrido-
[3 ,4-b]indole-8-yl)methyl)amine
Example 13A: 2-Ethoxycarbonyl-l,2,5,6-tetrahydropyrido[3,4-b]indole-8- carboxylic acid
A 20 mL pressure tube was charged with 4-carboxyphenylhydrazine (0.32g, 2.1 mmol), l-ethoxycarbonyl-4-ρiρeridone (0.34 g, 2.0 mmol) and acetic acid (4 mL). The suspension was heated with stirring for 2 minutes at 100W in a microwave oven to form the hydrazone intermediate. Polyphosphoric acid was then added (1 g) and the resulting yellow suspension was heated in the microwave oven for 2 minutes and then for further 2 minutes at 100W. The reaction mixture was then poured into hot water (30 mL) and the product separated as a gray solid (0.37 g). C15Hι6N2O4 Mass (calculated): [288]; (found): [M+H1"] = 289
NMR (400 MHz, dmso-d6): 1.2 (3H, d, 7= 6 Hz, CH3CH2O); 2.75-2.85 (2H, m, CCH2CH2N); 3.7-3.8 (2H, m, CCH2CH2N); 4.05 (2H, q, 7 = 6 Hz, CH3CH2O); 4.55-4.65 (2H, m, CCH2N); 7.35 (IH, d, 7 = 8 Hz, aryl-H); 7.7 (IH, dd, 7 = 1 and 8 Hz, aryl-H); 8.1 (IH, d, 7= 1 Hz, aryl-H).
Example 13B: Ethyl 5-ethyl-2-ethoxycarbonyl-l,2,5,6-tetrahydropyrido[3,4- b]indole-8-carboxylate
A solution of 2-ethoxycarbonyl-l,2,3,4-tetrahydropyrido[4,3-b]indole-8- carboxylic acid (0.35 g, 1.22 mmol) in dry DMF (10 mL) was cooled to 0 °C and sodium hydride (60% suspension in mineral oil, 0.122 g, 3.04 mmol) was added and the mixture was stirred for 30 minutes. Ethyl iodide (0.21 mL, 2.68 mmol) was then added and the reaction was allowed to reach room temperature and was stirred for further 24 hours. The reaction mixture was then diluted with ethyl acetate and water and extracted. The organic layer was washed with brine, dried over sodium sulfate, and the solvent removed under reduced pressure to give a crude which was purified by column chromatography (DCM/MeOH 98/2) to afford 0.367 g of the title compound.
C19H24N2O4 Mass (calculated): [344]; (found): [M+H4] = 345. NMR (400 MHz, CDC13): 1.3-1.4 (6H, m, CH3CH2O and CH3CH2N); 1.45 (3H, d, 7 = 6 Hz, CH3CH2O); 2.75-2.85 (2H, m, CCH2CH2N); 3.8-3.95 (2H, m,
CCH2CH2N); 4.5 (2H, bq, 7 = 6 Hz, CH3CH2N); 4.2 (2H, q, 7 = 6 Hz, CH3CH2O); 4.4 (2H, q, 7= 6 Hz, CH3CH2O); 4.7-4.8 (2H, bs, CCH2N); 7.25-7.3 (IH, m, aryl- H); 7.9 (IH, d, 7 = 8 Hz, aryl-H); 8.2 (IH, s, aryl-H).
Example 13C: 5-Ethyl-8-hydroxymethyl-2-methyl-l,2,5,6-tetrahydropyrido-
[3,4-b]indole Ethyl 5-ethyl-2-ethoxycarbonyl-l,2,3,4-tetrahydropyrido[4,3-b]indole-8- carboxylate (0.77 g, 2.25 mmol) was added to a ice-cold solution of lithium aluminum hydride (0.188 g, 4.5 mmol) in anhydrous THF (10 mL) and the reaction was stirred for 4 hours. Sodium hydroxide was then added dropwise (5% solution, 0.61 mL) and the mixture filtered through diatomaceous earth to afford the title compound.
Cι5H20N2O Mass (calculated): [244]; (found): [M+H4"] = 245. NMR (400 MHz, CDC13): 1.3 (3H, d, 7= 6 Hz, CH3CH2N); 2.5 (3H, s, NCH3); 2.8 (4H, bs, CCH2CH2N); 3.5 (2H, bs, CCH2N); 4.0 (2H, q, 7= 6 Hz, CH3CH2N); 4.65 (2H, s, CH2OH); 7.1 (IH, d, 7 = 8 Hz, aryl-H); 7.2 (IH, d, 7 = 8 Hz, aryl-H); 7.25 (IH, s, aryl-H).
Example 13D: 5-Ethyl-2-methyl-l ,2,5,6-tetrahydropyrido[3,4-b]indole-8- carboxaldehyde A solution of 5-Ethyl-8-hydroxymethyl-2-methyl-l,2,3,4-tetrahydropyrido[4,3- b]indole (0.73 g, 2.98 mmol) in acetone (40 mL) was treated with MnO2 (3.66 g) and stirred at room temperature for 72 hours. The solid was filtered and the solvent removed in vacuo to afford 0.67 g of title compound.
Cι5H18N2O Mass (calculated): [242]; (found): [M+H4] = 243. NMR (400 MHz, CDC13): 1.3 (3H, d, 7 = 6 Hz, CH3CH2N); 2.55 (3H, s, NCH3);
2.8 (4H, bs, CCH2CH2N); 3.65 (2H, bs, CCH2N); 4.05 (2H, q, 7= 6 Hz, CH3CH2N); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.7 (IH, dd, 7= 1 and 8 Hz, aryl-H);
7.9 (lH, d, 7= 1, aryl-H).
Example 13E:. (R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-2-methyl-l,2,5,6- tetrahydropyrido[3,4-b]indole-8-yl)methyl)amine
Prepared according to general procedure C.
C23H29Ν3 Mass (calculated): [347]; (found): [M+H4"] = 348.
NMR (400 MHz, CDC13): 1.25 (3H, t, 7 = 6 Hz, CH3CH2N); 1.3 (3H, d, 7 = 6 Hz, CH3CHN); 2.5 (3H, s, NCH3); 2.85 (4H, bs, CCH2CH2N); 3.55-3.65 (3H, m,
CCH2N and aryl-CH2N); 3.7 (IH, d, 7 = 12 Hz, aryl-CH2N); 4.0 (2H, q, 7 = 6 Hz, CH3CH2N); ); 7.0 (IH, dd, 7= 1 and 8 Hz, aryl-H); 7.15-7.25 (3H, m, aryl-H); 7.3-7.4 (4H, m, aryl-H).
Example 14
Figure imgf000035_0001
(R)-N-(l-((3-Methoxyphenyl)ethyl)-N-((5-ethyl-2-methyl-l,2,5,6- tetrahydropyrido [3 ,4-b]indole-8-yl)methyl)amine Prepared according to general procedure C.
Figure imgf000035_0002
227, 378. ΝMR (400 MHz, CDC13): 1.25 (3H, t, 7 = 6 Hz, CH3CH2Ν); 1.3 (3H, d, 7 = 6 Hz, CH3CHN); 2.5 (3H, s, NCH3); 2.8 (4H, bs, CCH2CH2N); 3.55-3.8 (8H, m, CCH2N, aryl-CH2N, CH3CH2N and OCH3); 4.0 (2H, q, 7= 6 Hz, CH3CH2N); ); 6.7-6.8 (IH, m, aryl-H); 6.85-6.9 (IH, m, aryl-H); 7.0 (IH, dd, 7 = 1 and 8 Hz, aryl-H); 7.1-7.3 (4H, m, aryl-H).
Example 15
Figure imgf000035_0003
(R)-N-(l-(l-Naρhthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine Prepared according to general procedure C. C27H26 Ν2O Mass (calculated): [378] (found): [M+H4"] = 379. NMR (400 MHz, CDC13): 1.5 (3H, t, 7=7 Hz, CH3CH2); 1.65 (3H, d, 7=7 Hz, NCHCH3); 3.9 and 4.0 (2H, dd, 7=14 Hz, CH2N); 4.4 (2H, q, 7=7 Hz, CH3CH2); 4.85 (IH, q, 7=7 Hz, NCHMe); 7.25 (IH, t, 7=7 Hz, aryl-H); 7.35-7.55 (6H, m, aryl-H); 7.6 (IH, t, 7=7 Hz, aryl-H); 7.85 (IH, d, 7=7 Hz); 7.9-8 (2H, m, aryl-H); 8 (IH, s, aryl-H); 8.05 (IH, d, 7=7 Hz, aryl-H); 8.2 (IH, bd, 7=7 Hz; aryl-H).
Example 16
Figure imgf000036_0001
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine Prepared according to general procedure C.
C24H26 Ν2O Mass (calculated): [358] (found): [M+H4"] = 359. NMR (400 MHz, CDC13): 1.3-1.4 (6H, m, NCHCH3 and CH2CH3); 3.7 (IH, d, 7= 12 Hz, CH2N); 3.75-3.83 (5H, m, CH2N, CHCH3, OCH3); 4.3 (2H, q, 7= 7 Hz, CH2CH3); 6.75 (IH, m, aryl-H); 6.9 (2H, m, aryl-H); 7.1-7.42 (6H, m, aryl-H); 7.9 (IH, s, aryl-H); 8.0 (IH, d, 7= 7 Hz, aryl-H).
Example 17
Figure imgf000036_0002
(R)-N-(l-(Phenyl)ethyl)-N-(9-ethyl-3-caι-bazolylmethyl)amine Prepared according to general procedure A. C24H26 N2O Mass (calculated): [328] (found): [M+H4"] = 208, 329. NMR (400 MHz, CDC13): 1.3-1.4 (6H, m, NCHCH3 and CH2CH3); 3.7 (IH, d, 7= 12 Hz, CH2N); 3.75-3.83 (5H, m, CH2N, CHCH3, OCH3); 4.3 (2H, q, 7= 7 Hz, CH2CH3); 6.75 (IH, m, aryl-H); 6.9 (2H, m, aryl-H); 7.1-7.42 (6H, m, aryl-H); 7.9 (IH, s, aryl-H); 8.0 (IH, d, 7= 7 Hz, aryl-H).
Figure imgf000037_0001
(R)-N-(l-(l-Naphthyl)ethyl)-N-((l-ethylindole-5-yl)methyl)amine Prepared according to general procedure C.
C23H24Ν2 Mass (calculated): [328] (found): [M+H4"] = 329, 157.
NMR (400 MHz, CDC13): 1.29 (3H, t, 7= 7.6 Hz, CH2CH3); 1.39 (3H, d, 7= 6.6
Hz; CHCH3); 3.67 and 3.76 (2H, dd, 7= 12.7 Hz, CH2N); 4.0 (2H, q, 7= 7.6 Hz,
CH2CH3); 4.6 (IH, q, 7= 6.6 Hz, CHCH3); 6.32 (IH, d, 7= 3 Hz, indole-H); 6.95 (IH, d, 7= 3 Hz, indole-H); 7.05 (IH, dd, 7= 1.5 and 8 Hz, aryl-H); 7.16 (IH, d,
7= 8.6 Hz, aryl-H); 7.3-7.5 (3H, m, aryl-H); 7.63 (IH, d, 7= 7.6 Hz, aryl-H); 7.7-
7.8 (2H, m, aryl-H); 8.0-8.1 (IH, m, aryl-H).
Figure imgf000038_0001
(R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[3,4-b]indole- 8-yl)methyl)amine
Example 19A: Methyl l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxylate Tetrahydro-4H-pyran-4-one (1.3 g, 13 mmol), 4-amino-3-iodobenzoic acid methyl ester (3.46 g, 12.5 mmol), DABCO (4.37 g, 39 mmol), MgSO4 (2.35 g, 19.5 mmol) and Pd(OAc)2 (0.15 g, 0.00065 mol) were dissolved in DMF (18 mL) and heated under nitrogen at 105 °C for 2 days. The reaction mixture was then partitioned between ethyl acetate and water, and extracted. The crude was purified by column chromatography (98/2 DCM/MeOΗ) to give 0.62 g of title compound. Cι3Η13ΝO3 Mass (calculated): [231] (found): [M+H4] = 232. NMR (400 MHz, acetone-d6): 2.7-2.8 (2H, m, CCH2CH2O); 3.8 (3H, s, CH3O); 3.8-3.85 (2H, m, CCH2CH2O); 4.75-4.8 (2H, m, CCH2O); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.65 (IH, dd, 7= 1 and 8 Hz); 8 (IH, d, 7= 1 Hz, aryl-H).
Example 19B: Methyl 5-ethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole-8- carboxylate
Ethyl l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxylate (0.62 g, 2.68 mmol) was dissolved in DMF (10 mL) and cooled to 0 °C. Sodium hydride (60% suspension in mineral oil, 0.16 g, 6.7 mmol) was added and the mixture stirred for 45 min prior to addition of ethyl iodide (0.50 g, 3.22 mmol). The mixture was stirred for 15 hours, then quenched with water and extracted with ethyl acetate. The organic layer was then removed and the crude was redissolved in acetonitrile and then washed with hexane to remove the mineral oil. The acetonitrile layer was evaporated to afford 0.5 g of title compound. Cι5H17NO3 Mass (calculated): [259] (found): [M+H4"] = 260. NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 2.7-2.8 (2H, m, CCH2CH2O); 3.8 (3H, s, CH3O); 3.9-4.0 (4H, m, CCH2CH2O and CH3CH2N); 4.9-4.95 (2H, m, CCH2O); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.75 (IH, dd, 7= 1 and 8 Hz); 8 (IH, d, 7= 1 Hz, aryl-H).
Example 19C: 5-Ethyl-8-hydroxymethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole Ethyl l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxylate (0.56 g, 2.16 mmol) was dissolved in dry THF (30 mL) and lithium aluminum hydride (1M in THF, 10.82 mL, 10.82 mmol) was added via syringe. The mixture was heated to reflux for one hour then cooled and NaOH (5% aqueous solution, 2.67 mL) was added. The mixture was filtered through diatomaceous earth and the solvent was removed to afford 0.5 g of title compound.
Ci4H17NO2 Mass (calculated): [231] (found): [M+H4"] = 232. NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 2.7-2.8 (2H, m, CCH2CH2O); 3.9-4.0 (4H, m, CCH2CH2O and CH3CH2N); 4.65 (2H, s, CH2OH); 4.8-4.85 (2H, m, CCH2O); 7.1 (IH, d, 7= 8 Hz, aryl-H); 7.35 (IH, d, 7= 8 Hz); 7.4 (IH, s, aryl-H).
Example 19D: 5-Ethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole-8-carboxyaldehyde 5-ethyl-8-hydroxymethyl-l,2,5,6-tetrahydropyrido[3,4-b]indole (0.5 g, 2.16 mmol) was dissolved in acetone (20 mL) and MnO2 (2.6 g) was added. The mixture was stirred for 24 hours then filtered and the filtrate concentrated in vacuo to afford 0.36 g of title compound.
Cι4H15NO2 Mass (calculated): [229] (found): [M+H4"] = 230
NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 2.7-2.8 (2H, m,
CCH2CH2O); 4.0-4.1 (4H, m, CCH2CH2O and CH3CH2N); 4.9-4.95 (2H, m, CCH2O); 7.3 (IH, d, 7= 8 Hz, aryl-H); 7.7 (IH, d, 7= 8 Hz); 7.9 (IH, s, aryl-H);
10 (IH, s, CHO) Example l9E: (R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[3,4- b]indole-8-yl)methyl)amine Prepared according to general procedure C. C 2Η26Ν2O Mass (calculated): [334] (found): [M+H4"] = 335. NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 1.3 (3H, d, 7= 6 Hz, CH3CHN); 2.7-2.8 (2H, m, CCH2CH2O); 3.6 and 3.7 (2H, dd, 7= 12 Hz, aryl- CH2N); 3.8 (IH, q, 7= 6 Hz, CH3CHN); 3.9-4.05 (4H, m, CH2CH2O and CH3CH2N); 4.85-4.9 (2H, , CCH2O); 7.05 (IH, dd, 7= 1 and 8 Hz, aryl-H); 7.15-7.25 (3H, m, aryl-H); 7.3-7.4 (4H, m, aryl-H).
Figure imgf000040_0001
(R)-N-(l-((3-Methoxyphenyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[3,4- b]indole-8-yl)methyl)amine Prepared according to general procedure C.
C23Η28Ν2O2 Mass (calculated): [364] (found): [M+H4"] = 365.
NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 1.3 (3H, d, 7= 6 Hz,
CH3CHN); 2.7-2.8 (2H, m, CCH2CH2O); 3.6 and 3.7 (2H, dd, 7= 12 Hz, aryl-
CH2N); 3.8-3.9 (4H, m, CH3O and CH3CHN); 3.9-4.05 (4H, m, CH2CH2O and CH3CH2N); 4.85-4.9 (2H, m, CCH2O); 6.75 (IH, dd, 7= 1 and 8 Hz, aryl-H); 7.05
(IH, dd, 7= 2 and 8 Hz, aryl-H); 6.8-6.9 (2H, m, aryl-H); 7.05 (IH, dd, 7= 1 and 8
Hz, aryl-H); 7.2-7.4 (3H, m, aryl-H).
Example 21
Figure imgf000041_0001
(R)-N-(l-((l-naphthyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[4,3-b]indole-8- yl)methyl)amine
Prepared according to general procedure C.
C22Η28Ν2O Mass (calculated): [384] (found): [M+H4] = 385.
NMR (400 MHz, CDC13): 1.25 (3H, t, 7= 6 Hz, CH3CH2N); 1.45 (3H, d, 7= 6 Hz,
CH3CHN); 2.7-2.8 (2H, m, CCH2CH2O); 3.7 and 3.8 (2H, dd, 7= 12 Hz, aryl-
CH2N); 3.9-4.05 (4H, m, CH2CH2O and CH3CH2N); ); 4.8 (IH, q, 7= 6 Hz,
CH3CHN); 4.85-4.9 (2H, m, CCH2O); 7.0-7.2 (3H, m, aryl-H); 7.35-7.55 (3H, m, aryl-H); 7.7 (IH, d, 7= 8 Hz, aryl-H); 7.8-7.85 (2H, m, aryl-H); 7.9-8 (IH, m, aryl-H)
Example 22
H r
Figure imgf000041_0002
(R)-N-(l-(Phenyl)ethyl)-N-(9-(3-(N,N-dimethylamino)propyl)-3- carbazolylmethyl)amine
Example 22A: 9-(3-chloropropyl)carbazole Prepared as in WO9634863. Cι5Hι4ClN Mass (calculated): [243].
2.3 (2H, quintet, 7= 6 Hz, C1CH2CH2CH2N); 3.4 (2H, t, 7= 6 Hz, C1CH2CH2CH2N); 4.45 (2H, t, , 7= 6 Hz, C1CH2CH2CH2N); 7.15-7.25 (2H, m, aryl-H); 7.35-7.45 (4H, m, aryl-H); 8.0-8.1 (2H, m, aryl-H).
Example 22B: 9-(3-(N,N-dimethylamino)propyl)carbazole 9-(3-chloropropyl)carbazole (2.5 g, 10 mmol) was dissolved in acetonitrile (50 mL) in a pressure tube and dimethylamine hydrochloride (12.2 g, 150 mmol, followed by K2CO3 (20.8 g, 150 mmol) and potassium iodide (0.2 g, 1 mmol) were added and the mixture was stirred at room temperature for 7 days, then filtered and the filtrate concentrated in vacuo. The crude was purified by column chromatography (eluting with 5% methanol in dichloromethane) to afford 1.87 g of the title compound. Cι7H2oΝ2
Mass (calculated): [252] (found): [M+H4"] = 253
Example 22C: 9-(3-(N,N-Dimethylamino)propyl)carbazole-3-carboxyaldehyde A solution of 9-(3-(N,N-dimethylamino)propyl)carbazole (0.37 g, 1.45 mmol) was dissolved in dichloromethane (6 mL) and the solution cooled to 0 °C. Aluminum trichloride (0.39 g, 2.91 mmol) was then added and the mixture was stirred for 10 minutes. A solution of dichloromethyl methyl ether (0.17 g, 1.45 mmol) in dichloromethane (3 mL) was then added dropwise to the ice-cold mixture and reaction stirred at 0 °C for 4 hours. Water (10 mL) was then added and the pH adjusted to 9 by addition of potassium carbonate. The mixture was stirred for 16 hours then extracted with dichloromethane. The organic layer was dried over sodium sulfate to afford 0.3 g of the title compound.
Mass (calculated): [280] (found): [M+H*] = 281
1.95 (2H, quintet, 7= 6 Hz, ΝCH2CH2CH2Ν); 2.15 (6H, s, (CH3)2N); 2.2 (2H, t, 7= 6 Hz, NCH2CH2CH2N); 4.35 (2H, t, , 7= 6 Hz, NCH2CH2CH2N); 7.25-7.3 (IH, m, aryl-H); 7.45-7.55 (3H, m, aryl-H); 7.95 (IH, dd, 7= 1 and 8 Hz, aryl-H); 8.1 (IH, d, 7= 8 Hz, aryl-H); 8.55 (IH, d, 7= 1 Hz, aryl-H); 10.0 (IH, s, CHO). Example 22D: (R)-N-(l-(Phenyl)ethyl)-N-(9-(3-(N,N-dimethylamino)propyl)-3- carbazolylmethyl)amine Prepared according to general procedure C. C26H31Ν3 Mass (calculated): [385] (found): [M+H4"] = 500, 386.
NMR (400 MHz, CDC13): 1.3 (3H, t, 7= 6 Hz, NCHCH3); 1.95 (2H, quintet, 7= 6 Hz, NCH2CH2CH2N); 2.15 (6H, s, (CH3)2N); 2.2 (2H, t, 7= 6 Hz, NCH2CH2CH2N): 3.7 and 3.75 (2H, dd, 7= 12 Hz, aryl-CH2N); 3.8 (IH, q, 7= 6 Hz, CHCH3); 4.3 (2H, t, , 7= 6 Hz, NCH2CH2CH2N); 7.1-7.3 (2H, m, aryl-H); 7.4-7.5 (8H, m, aryl-H); 7.9 (IH, s, aryl-H); 8.05 (IH, d, , 7= 8 Hz, aryl-H).
Example 23
Figure imgf000043_0001
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-(3-(N,N-dimethylamino)propyl)-3- carbazolylmethyl)amine
Prepared according to general procedure C.
C27H33Ν3O Mass (calculated): [415] (found): [M+H4"] = 530, 416.
NMR (400 MHz, CDC13): 1.3 (3H, t, 7= 6 Hz, NCHCH3); 1.95 (2H, quintet, 7= 6
Hz, NCH2CH2CH2N); 2.15 (6H, s, (CH3)2N); 2.2 (2H, t, 7= 6 Hz, NCH2CH2CH2N): 3.7-3.85 (6H, m, aryl-CH2N, CH3O and CHCH3); 4.3 (2H, t, ,
7= 6 Hz, NCH2CH2CH2N); 6.7-6.75 (IH, m, aryl-H); 6.9-6.95 (2H, m, aryl-H);
7.1-7.2 (IH, m, aryl-H); 7.3 (IH, t, 7= 6 Hz, aryl-H); 7.35-7.4 (2H, m, aryl-H), 7.4
(2H, m, aryl-H); 7.9 (IH, s, aryl-H); 8.05 (IH, d, , 7= 8 Hz, aryl-H). Example 24
Figure imgf000044_0001
(R)-N-(l-(l-Naphthyl)phenyl)ethyl)-N-(9-(3-(N,N-dimethylamino)propyl)-3- carbazolylmethyl)amine
Prepared according to general procedure C.
C30H33Ν3 Mass (calculated): [434] (found): [M+H4"] = 436, 155, 265.
NMR (400 MHz, CDC13): 1.45 (3H, t, 7= 6 Hz, NCHCH3); 1.95 (2H, quintet, 7= 6
Hz, NCH2CH2CH2N); 2.15 (6H, s, (CH3)2N); 2.2 (2H, t, 7= 6 Hz,
NCH2CH2CH2N); 3.75 and 3.85 (2H, dd, 7= 12 Hz, aryl-CH2N); 4.3 (2H, t, , 7= 6
Hz, NCH2CH2CH2N); 4.7 (IH, q, 7= 6 Hz, CHCH3); 7.15-7.2 (IH, m, aryl-H); 7.4
(2H, s, aryl-H); 7.45-7.5 (4H, m, aryl-H); 7.55 (IH, t, 7= 8 Hz, aryl-H); 7.7 (IH, d, 7= 8 Hz, aryl-H); 7.75 (IH, d, 7= 8 Hz, aryl-H); 7.9 (IH, s, aryl-H); 7.95 )1H, d, 7= 8 Hz, aryl-H); 8.1-8.15 (IH, m, aryl-H).
The following compounds were prepared according to General Method C:
Example 25
(lR)-N-(lH-indol-5-ylmethyl)-l-(l-naphthalenyl)ethanamine
Figure imgf000044_0002
MW 300.41 Mass found: 301
Example 26
(lR)-N-((l-ethyl-lH-indol-5-yl)methyl)-l-(l-naphthalenyl)ethanamine
Figure imgf000045_0001
MW 328.457 Mass found: 158, 329
Example 27
(lR)-N-((l-ethyl-3-phenyl-lH-indol-5-yl)methyl)-l-(l-naphthalenyl)ethanamine
Figure imgf000045_0002
MW 404.554 Mass found: 234, 405
Example 28
( lR)-N-(( 1 -ethyl-3 -phenyl- lH-indol-5-yl)methyl)- 1 -phenylethanamine
Figure imgf000045_0003
MW 354.494 Mass found: 234, 355, 709
Example 29
(lR)-N-((l-ethyl-3-(4-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000046_0001
MW 438.491 Mass found: 318, 439
Example 30
(lR)-N-((l-ethyl-3-(4-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000046_0002
MW 488.55 Mass found: 489, 977
Example 31 (lR)-N-((l-ethyl-3-(3-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000047_0001
MW 438.491 Mass found: 318, 439
Example 32
(lR)-N-((l-ethyl-3-(3-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000047_0002
MW 488.55 Mass found: 318, 489
Example 33
(lR)-N-((l-ethyl-3-(3-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000047_0003
MW 422.491 Mass found: 302
Example 34 (lR)-N-((l-ethyl-3-(3-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000048_0001
MW 472.551 Mass found: 302, 473
Example 35
(lR)-N-((l-ethyl-3-(3-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l-(3-
(methyloxy)phenyl)ethanamine
Figure imgf000048_0002
MW 452.517 Mass found: 302
Example 36
(lR)-N-((l-ethyl-3-(3-(methyloxy)phenyl)-lH-indol-5-yl)methyl)-l-(3- (methyloxy)phenyl)ethanamine
Figure imgf000049_0001
MW 414.546 Mass found: 264
Example 37
(lR)-N-((l-ethyl-3-(3-(methyloxy)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000049_0002
MW 384.52 Mass found: 385, 264, 769
Example 38
(lR)-N-((l-ethyl-3-(3-(methyloxy)phenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000049_0003
MW 434.58 Mass found: 435, 264 Example 39
(lR)-N-((l-ethyl-3-(3-fluorophenyl)-lH-indol-5-yl)methyl)-l-phenylethanamine
Figure imgf000050_0001
MW 372.484 Mass found: 252, 373, 745
Example 40
(lR)-N-((l-ethyl-3-(3-fluorophenyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000050_0002
MW 422.544 Mass found: 423, 252
Example 41
(lR)-N-((3-(3-chlorophenyl)-l-ethyl-lH-indol-5-yl)methyl)-l-phenylethanamine
Figure imgf000050_0003
MW 388.94 Mass found: 268, 389, 777
Example 42
(lR)-N-((3-(3-chlorophenyl)-l-ethyl-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000051_0001
MW 439.00 Mass found: 439, 268
Example 43
(lR)-N-((l-ethyl-3-(4-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000051_0002
MW 422.491 Mass found: 423, 302
Example 44
(lR)-N-((l-ethyl-3-(4-(trifluoromethyl)phenyl)-lH-indol-5-yl)methyl)-l-(l-
Figure imgf000052_0001
MW 472.551 Mass found: 473, 302
Example 45
(lR)-N-((l-ethyl-2-(2-pyridinyl)-lH-indol-5-yl)methyl)-l-(l- naphthalenyl)ethanamine
Figure imgf000052_0002
MW 405.542 Mass found: 235, 253, 406
Example 46
(lR)-N-((l-ethyl-2-(2-pyridinyl)-lH-indol-5-yl)methyl)-l-(3- (methyloxy)phenyl)ethanamine
Figure imgf000052_0003
MW 385.508 Mass found: 235, 253, 386
Example 47
(lR)-N-((l-ethyl-2-(2-p )-l-phenylethanamine
Figure imgf000053_0001
MW 355.483 Mass found: 253, 235, 356
Example 48
(lR)-N-((l-ethyl-2-phenyl-lH-indol-5-yl)methyl)-l-phenylethanamine
Figure imgf000053_0002
MW 354.494 Mass found: 234, 355
Example 49 (lR)-N-((l-ethyl-2-phenyl-lH-indol-5-yl)methyl)-l-(l-naphthalenyl)ethanamine
Figure imgf000053_0003
MW 404.5540 Mass found: 234, 405
Example 50
(lR)-N-((l-ethyl-2-phenyl-lH-indol-5-yl)methyl)-l-(3- (methyloxy)phenyl)ethan amine
Figure imgf000054_0001
MW 384.52
Mass found: 234, 385
Example 51
(lR)-l-ρhenyl-N-((l-(4-(trifluoromethyl)phenyl)-lH-indol-5- yl)methyl)ethanamine
Figure imgf000054_0002
MW 394.438 Mass found: 274, 395
Example 52
(lR)-l-(l-naphthalenyl)-N-((l-(4-(trifluoromethyl)phenyl)-lH-indol-5- yl)methyl)ethanamine
Figure imgf000055_0001
MW 444.498 Mass found: 274, 445
Example 53
( IR)- 1 -(3 -(methyloxy)phenyl)-N-((l -(4-(trifluoromethyl)phenyl)- lH-indol-5-
Figure imgf000055_0002
MW 424.464 Mass found: 274, 425
Example 54 (lR)-N-((l-ethyl-3-(l,3-oxazol-5-yl)-lH-indol-5-yl)methyl)-l-ρhenylethanamine
Figure imgf000055_0003
MW 345.444 Mass found: 225, 346, 691 Example 55
(lR)-N-((l-ethyl-3-(l-methyl-lH-imidazol-5-yl)-lH-indol-5-yl)methyl)-l- phenylethanamine
Figure imgf000056_0001
MW 358.486
Mass found: 359, 255
Biological Activity
The activities of the compounds of the present invention on calcium receptors were measured. In one embodiment, the measurement was performed in accordance with the method described in Example 4 of Nemeth et al., PCT/US95/13704 (International Publication No. WO96/12697) herein incorporated by reference.
A 4.0-kb Notl-Hind-XT fragment of the human parathyroid cell Ca24" receptor (hPCaR) cDΝA was subcloned into the mammalian expression vector pCEP4 (Invitrogen) containing the hygromycin-resistant gene as a selectable marker. This plasmid was transfected into HEK 293 cells by calcium phosphate precipitation. Transfected cells were grown in Dulbecco's modified Eagle's medium containing 10% fetal bovine serum and hygromycin (200 μg/mL). Hygromycin-resistant colonies were subcloned and assayed for hPCaR mRΝA by solution hybridization using a 32P-labeled RΝA probe complementary to the (4.0 kb) hPCaR sequence (Garrett, et al., J. Biol. Chem. 270, 12919-12925 (1995)). Clone 7 was used to assess the effects of compounds on [Ca2+]j. This stably transfected cell line is termed HEK 293 4.0-7. For measurements of [Ca2+]i, the cells were recovered from tissue culture flasks by brief treatment with 0,02%
EDTA and then washed and resuspended in PCB containing ImM CaCl2 and 0.1% Bovine Serum Albumin ("BSA"). The cells were loaded with fluo-3 by incubation for 30 min at 37°C, with parathyroid cell buffer (126mM NaCl, 4mM
KC1, lmM MgSO4, 0.7mM KaHPO-TK^PO^ 20mM HEPES-NaOH (pH 7.45)) containing 0.5% BSA in lmM CaCl2 and 2μM fluo-3 acetoxymethyl ester. The cells were subsequently washed, each test compound was added to the cells and the fluorescence was recorded by using excitation and emission wavelengths of
485 and 530 nm, respectively.
The following compounds of the invention were tested acording to the procedure described above and found to have an EC50 of 10 μM or less:
(R)-N-(l-(l-Naphthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine; (R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine;
(R)-N-( 1 -(1 -Νaphthyl)ethyl)-N-( 1 -ethyl-5-indolylmethyl)amine;
(R)-N-(l-(l-Νaphthyl)ethyl)-N-(2'-ethyl-benzotriazol-5-ylmethyl)amine;
(R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(2'-ethyl-benzotriazol-5-ylmethyl)amine;
(T )-N-(l-(Phenyl)ethyl)-N-(2'-ethyl-benzotriazol-5-ylmethyl)amine; (R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-6-methoxy-3-carbazolylmethyl)- amine;
(R)-N-(l-((Phenyl)ethyl)-N-((l-ethylcyclopent[b]indol-5-yl)methyl)amine;
(R)-N-(l-(l-Νaphthyl)ethyl)-N-((l-methylbenzimidazol-5-yl)methyl)amine;
(R)-N-(l-(Phenyl)ethyl)-N-((l-methylbenzimidazol-5-yl)methyl)amine; (R)-N-( 1 -((Phenyl)ethyl)-N-((5-ethyl-2-methyl- 1 ,2,5 ,6-tetrahydropyrido-
[3 ,4-b]indole-8-yl)methyl)amine;
(R)-N-(l-((3-Methoxyphenyl)ethyl)-N-((5-ethyl-2-methyl-l,2,5,6- tetrahydropyrido [3 ,4-b] indole- 8 -yl)methyl)amine ; (R)-N-(l-(l-Νaphthyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine; (R)-N-(l-(3-Methoxyphenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine; (R)-N-(l-(Phenyl)ethyl)-N-(9-ethyl-3-carbazolylmethyl)amine; (R)-N-(l-(l-Νaphthyl)ethyl)-N-((l-ethylindole-5-yl)methyl)amine; (R)-N-(l-((Phenyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[3,4-b]indole- 8-yl)methyl)amine; (R)-N-(l-((3-Methoxyphenyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[3,4- b]indole-8-yl)methyl)amine; (R)-N-(l-((l-naphthyl)ethyl)-N-((5-ethyl-5,6-dihydro-2H-pyrano[4,3-b]indole-8- yl)methyl)amine;
(R)-N-(l-(l-Νaphthyl)phenyl)ethyl)-N-(9-(3-(N,N-dimethylamino)propyl)-3- carbazolylmethyl)amine; (lR)-Ν-(lΗ-indol-5-ylmethyl)-l-(l-naphthalenyl)ethanamine;
(lR)-N-((l-ethyl-lH-indol-5-yl)methyl)-l-(l-naphthalenyl)ethanamine;
( lR)-N-(( 1 -ethyl-3 -phenyl- 1 H-indol-5 -yl)methyl)- 1 -phenylethanamine ;
(lR)-N-((l-ethyl-3-(4-((trifluoromethyl)oxy)phenyl)-lH-indol-5-yl)methyl)-l- phenylethanamine ; For the treatment of bone disorders, such as osteoporosis, excessive secretion of PTH, such as hyperparathyroidism, and the like, the compounds of the present invention may be administered orally, parentally, by inhalation spray, rectally, or topically in dosage unit formulations containing conventional pharmaceutically acceptable carriers, adjuvants, and vehicles. The term parenteral as used herein includes, subcutaneous, intravenous, intramuscular, intrasternal, infusion techniques or intraperitoneally.
Treatment of diseases and disorders herein is intended to also include the prophylactic administration of a compound of the invention, a pharmaceutical salt thereof, or a pharmaceutical composition of either to a subject (i.e., an animal, preferably a mammal, most preferably a human) believed to be in need of preventative treatment, such as, for example, pain, inflammation and the like. The dosage regimen for treating the disclosed diseases with the compounds of this invention and/or compositions of this invention is based on a variety of factors, including the type of disease, the age, weight, sex, medical condition of the patient, the severity of the condition, the route of administration, and the particular compound employed. Thus, the dosage regimen may vary widely, but can be determined routinely using standard methods. Dosage levels of the order from about 0.01 mg to 30 mg per kilogram of body weight per day, preferably from about 0.1 mg to 10 mg/kg, more preferably from about 0.25 mg to 1 mg/kg are useful for all methods of use disclosed herein.
The pharmaceutically active compounds of this invention can be processed in accordance with conventional methods of pharmacy to produce medicinal agents for administration to patients, including humans and other mammals.
For oral administration, the pharmaceutical composition may be in the form of, for example, a capsule, a tablet, a suspension, or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a given amount of the active ingredient. For example, these may contain an amount of active ingredient from about 1 to 2000 mg, preferably from about 1 to 500 mg, more preferably from about 5 to 150 mg. A suitable daily dose for a human or other mammal may vary widely depending on the condition of the patient and other factors, but, once again, can be determined using routine methods.
The active ingredient may also be administered by injection as a composition with suitable carriers including saline, dextrose, or water. The daily parenteral dosage regimen will be from about 0.1 to about 30 mg/kg of total body weight, preferably from about 0.1 to about 10 mg/kg, and more preferably from about 0.25 mg to 1 mg/kg.
Injectable preparations, such as sterile injectable aqueous or oleaginous suspensions, may be formulated according to the known are using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed, including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.
Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient such as cocoa butter and polyethylene glycols that are solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum and release the drug. A suitable topical dose of active ingredient of a compound of the invention is 0.1 mg to 150 mg administered one to four, preferably one or two times daily. For topical administration, the active ingredient may comprise from 0.001% to 10% w/w, e.g., from 1% to 2% by weight of the formulation, although it may comprise as much as 10% w/w, but preferably not more than 5% w/w, and more preferably from 0.1% to 1% of the formulation.
Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin (e.g., liniments, lotions, ointments, creams, or pastes) and drops suitable for administration to the eye, ear, or nose.
For administration, the compounds of this invention are ordinarily combined with one or more adjuvants appropriate for the indicated route of administration. The compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, stearic acid, talc, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulphuric acids, acacia, gelatin, sodium alginate, polyvinyl-pyrrolidine, and/or polyvinyl alcohol, and tableted or encapsulated for conventional administration. Alternatively, the compounds of this invention may be dissolved in saline, water, polyethylene glycol, propylene glycol, ethanol, corn oil, peanut oil, cottonseed oil, sesame oil, tragacanth gum, and/or various buffers. Other adjuvants and modes of administration are well known in the pharmaceutical art. The carrier or diluent may include time delay material, such as glyceryl monostearate or glyceryl distearate alone or with a wax, or other materials well known in the art.
The pharmaceutical compositions may be made up in a solid form (including granules, powders or suppositories) or in a liquid form (e.g., solutions, suspensions, or emulsions). The pharmaceutical compositions may be subjected to conventional pharmaceutical operations such as sterilization and/or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers etc. Solid dosage forms for oral administration may include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound may be admixed with at least one inert diluent such as sucrose, lactose, or starch. Such dosage forms may also comprise, as in normal practice, additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.
Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water. Such compositions may also comprise adjuvants, such as wetting, sweetening, flavoring, and perfuming agents.
Compounds of the present invention can possess one or more asymmetric carbon atoms and are thus capable of existing in the form of optical isomers as well as in the form of racemic or non-racemic mixtures thereof. The optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, e.g. , by formation of diastereoisomeric salts, by treatment with an optically active acid or base. Examples of appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric, and camphorsulfonic acid and then separation of the mixture of diastereoisomers by crystallization followed by liberation of the optically active bases from these salts. A different process for separation of optical isomers involves the use of a chiral chromatography column optimally chosen to maximize the separation of the enantiomers. Still another available method involves synthesis of covalent diastereoisomeric molecules by reacting compounds of the invention with an optically pure acid in an activated form or an optically pure isocyanate. The synthesized diastereoisomers can be separated by conventional means such as chromatography, distillation, crystallization or sublimation, and then hydrolyzed to deliver the enantiomerically pure compound. The optically active compounds of the invention can likewise be obtained by using active starting materials. These isomers may be in the form of a free acid, a free base, an ester or a salt. Likewise, the compounds of this invention may exist as isomers, that is compounds of the same molecular formula but in which the atoms, relative to one another, are arranged differently. In particular, the alkylene substituents of the compounds of this invention, are normally and preferably arranged and inserted into the molecules as indicated in the definitions for each of these groups, being read from left to right. However, in certain cases, one skilled in the art will appreciate that it is possible to prepare compounds of this invention in which these substituents are reversed in orientation relative to the other atoms in the molecule. That is, the substituent to be inserted may be the same as that noted above except that it is inserted into the molecule in the reverse orientation. One skilled in the art will appreciate that these isomeric forms of the compounds of this invention are to be construed as encompassed within the scope of the present invention. The compounds of the present invention can be used in the form of salts derived from inorganic or organic acids. The salts include, but are not limited to, the following: acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, cyclopentanepropionate, dodecylsulfate, ethanesulfonate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, fumarate, hydrochloride, hydrobromide, hydroiodide, 2-hyroxy-ethanesulfonate, lactate, maleate, methansulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, palmoate, pectinate, persulfate, 2-phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, thiocyanate, tosylate, mesylate, and undecanoate. Also, the basic nitrogen-containing groups can be quatemized with such agents as lower alkyl halides, such as methyl, ethyl, propyl, and butyl chloride, bromides and iodides; dialkyl sulfates like dimethyl, diethyl, dibutyl, and diamyl sulfates, long chain halides such as decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides, aralkyl halides like benzyl and phenethyl bromides, and others. Water or oil-soluble or dispersible products are thereby obtained.
Examples of acids that may be employed to form pharmaceutically acceptable acid addition salts include such inorganic acids as hydrochloric acid, sulphuric acid and phosphoric acid and such organic acids as oxalic acid, maleic acid, succinic acid and citric acid. Other examples include salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium or magnesium or with organic bases. Also encompassed in the scope of the present invention are pharmaceutically acceptable esters of a carboxylic acid or hydroxyl containing group, including a metabolically labile ester or a prodrug form of a compound of this invention. A metabolically labile ester is one which may produce, for example, an increase in blood levels and prolong the efficacy of the corresponding non-esterified form of the compound. A prodrug form is one which is not in an active form of the molecule as administered but which becomes therapeutically active after some in vivo activity or biotransformation, such as metabolism, for example, enzymatic or hydrolytic cleavage. For a general discussion of prodrugs involving esters see Svensson and Tunek Drug Metabolism Reviews 165 (1988) and Bundgaard Design of Prodrugs, Elsevier (1985). Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl). Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989)). Also, drugs containing an acidic NH group, such as imidazole, imide, indole and the like, have been masked with N-acyloxymethyl groups (Bundgaard Design of Prodrugs, Elsevier (1985)). Hydroxy groups have been masked as esters and ethers. EP 039,051 (Sloan and Little, 4/11/81) discloses Mannich-base hydroxamic acid prodrugs, their preparation and use. Esters of a compound of this invention, may include, for example, the methyl, ethyl, propyl, and butyl esters, as well as other suitable esters formed between an acidic moiety and a hydroxyl containing moiety. Metabolically labile esters, may include, for example, methoxymethyl, ethoxymethyl, iso-propoxymethyl, α-methoxyethyl, groups such as α-((Cι-C4)alkyloxy)ethyl; for example, methoxyethyl, ethoxyethyl, propoxyethyl, iso-propoxyethyl, etc.; 2-oxo-l,3-dioxolen-4-ylmethyl groups, such as 5-methyl-2-oxo-l,3,dioxolen-4-ylmethyl, etc.; Cι-C3 alkylthiomethyl groups, for example, methylthiomethyl, ethylthiomethyl, isopropylthiomethyl, etc.; acyloxymethyl groups, for example, pivaloyloxymethyl, α-acetoxymethyl, etc.; ethoxycarbonyl-1 -methyl; or α-acyloxy- -substituted methyl groups, for example -acetoxyethyl.
Further, the compounds of the invention may exist as crystalline solids which can be crystallized from common solvents such as ethanol, N,N-dimethyl-formamide, water, or the like. Thus, crystalline forms of the compounds of the invention may exist as solvates and/or hydrates of the parent compounds or their pharmaceutically acceptable salts. All of such forms likewise are to be construed as falling within the scope of the invention.
While the compounds of the invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more compounds of the invention or other agents. When administered as a combination, the therapeutic agents can be formulated as separate compositions that are given at the same time or different times, or the therapeutic agents can be given as a single composition. The foregoing is merely illustrative of the invention and is not intended to limit the invention to the disclosed compounds. Variations and changes which are obvious to one skilled in the art are intended to be within the scope and nature of the invention which are defined in the appended claims.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

Claims

We Claim:
A compound of Formula (I):
Figure imgf000065_0001
(I) or a pharmaceutically acceptable salt thereof, wherein: == represents a double or single bond; R1 is Rb;
R2 is d-8alkyl or Cι-4haloalkyl; R3 is H, d-4haloalkyl or Cι.8alkyl;
R4 is H, Cι-4haloalkyl or Cι-8alkyl;
R5 is, independently, in each instance, H, d-8alkyl, Cι-4haloalkyl, halogen, -OCι-6alkyl, -NRaRd or NRdC(=O)Rd;
R6 is Rd, Cι-4haloalkyl, -C(=O)Rc, -OCι-6alkyl, -ORb, -NRaRa, -NRaR , -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa;
R7 is Rd, Cι-4haloalkyl, -C(=O)Rc, -OCι-6alkyl, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa; or R6 and R7 together form a 3- to 6-atom saturated or unsaturated bridge containing 0, 1, 2 or 3 N atoms and 0, 1 or 2 atoms selected from S and O, wherein the bridge is substituted by 0, 1 or 2 substituents selected from R ; wherein when R and R form a benzo bridge, then the benzo bridge may be additionally substituted by a 3- or 4- atoms bridge containing 1 or 2 atoms selected from N and O, wherein the bridge is substituted by 0 or 1 substituents selected from Cι-4alkyl;
Ra is, independently, at each instance, H, C^haloalkyl or d-6alkyl; Rb is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from d-6alkyl, halogen, d-4haloaιkyl, -Od-6alkyl, cyano and nitro; Rc is, independently, at each instance, d-6alkyl, Cι-4haloalkyl, phenyl or benzyl;
Rd is, independently, at each instance, H, C^a-kyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the Cι-6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from d-6alkyl, halogen, Cι-4haloalkyl, -Od-6alkyl, cyano and nitro, Rb, -C(=O)Rc, -ORb, -NRaRa, -NRaR , -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; X is -CRd=N-, -N=CRd-, O, S or -NRd-; when == is a double bond then Y is =CR6- or =N- and Z is -CR7= or -N= ; and when — is a single bond then Y is -CRaR6- or -NRd- and Z is -CRaR7- or -NRd-; and m is 1 or 2.
2. A compound or salt according to Claim 1, wherein R1 is phenyl substituted by 0, 1, 2 or 3 substituents selected from d-6alkyl, halogen, d- haloalkyl, -Od-6alkyl, cyano and nitro.
3. A compound or salt according to Claim 1, wherein R1 is benzyl substituted by 0, 1, 2 or 3 substituents selected from d-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro.
4. A compound or salt according to Claim 1, wherein R1 is naphthyl substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen,
Cι-4haloalkyl, -OCι-6alkyl, cyano and nitro.
5. A compound or salt according to Claim 1, wherein R1 a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 0, 1, 2 or 3 substituents selected from > Cι.6alkyl, halogen, Cι-4haloalkyl, -OCι-6alkyl, cyano and nitro.
A compound or salt according to Claim 1, wherein R and R4 are
H.
7. A compound or salt according to Claim 1, wherein R is H.
8. A compound or salt according to Claim 1, wherein R is H.
9. A compound or salt according to Claim 1, wherein R7 is H.
10. A compound or salt according to Claim 1, wherein X is -NRd-.
11. A compound or salt according to Claim 10, wherein = is a double bond; Y is =CR6- or =N-; and
Z is -CR7= or -N=.
12. A compound or salt according to Claim 10, wherein ^^ is a single bond; Y is -CRaR6- or -NRd-; and
Z is -CRaR7- or -NRd-.
13. A compound or salt according to Claim 1, having the structure of Formula (II):
Figure imgf000068_0001
(H) wherein:
R1 is R1
R .2 is d-8alkyl or Cι-4haloalkyl; R3 is H, Cι-4haloalkyl or Cι-8alkyl;
R >4 i •s H,
Figure imgf000068_0002
or d-8alkyl;
R is, independently, in each instance, H, d-salkyl, C^haloalkyl, halogen,
-OCι-6alkyl, -NRaRd or NRdC(=O)Rd; R6 is Rd, Cι-4haloalkyl, -C(=O)Rc, -Od-6alkyl, -ORb, -NRaRa, -NRaRb,
-C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro,
-NRaS(=O)mRc or -S(=O)mNRaRa;
R7 is Rd, d-4haloalkyl, -C(=O)Rc, -OCι-6alkyl, -ORb, -NRaRa, -NRaRb,
-C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, cyano, nitro, -NRaS(=O)mRc or -S(=O)mNRaRa; or R6 and R7 together form a 3- to 6-atom saturated or unsaturated bridge containing 0, 1, 2 or 3 N atoms and 0, 1 or 2 atoms selected from S and O, wherein the bridge is substituted by 0, 1 or 2 substituents selected from R ; wherein when R and R form a benzo bridge, then the benzo bridge may be additionally substituted by a 3- or 4- atoms bridge containing 1 or 2 atoms selected from N and O, wherein the bridge is substituted by 0 or 1 substituents selected from Cι-4alkyl;
Ra is, independently, at each instance, H, Cι-4haloalkyl or d-6alkyl; Rb is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from
O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι-4haloalkyl, -OCι.6alkyl, cyano and nitro; Rc is, independently, at each instance, Cι-6alkyl, Cι-4haloalkyl, phenyl or benzyl;
Rd is, independently, at each instance, H, d-6alkyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the d-6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from Cι_6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro, R , -C(=O)Rc, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; and m is 1 or 2.
14. A compound or salt according to Claim 1, having the structure
Figure imgf000069_0001
wherein:
R1 is Rb;
R2 is d-8alkyl or Cι-4haloalkyl; R3 is H, d-4haloalkyl or Cι-8alkyl; R4 is H, d-4haloalkyl or Cι-8alkyl; R5 is, independently, in each instance, H, Cι-8alkyl, d-4haloalkyl, halogen,
-OCι-6alkyl, -NRaRd or NRdC(=O)Rd;
Ra is, independently, at each instance, H, d.4haloalkyl or d-6alkyl; R is, independently, at each instance, phenyl, benzyl, naphthyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the phenyl, benzyl or heterocycle are substituted by 0, 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι- haloalkyl, -OCi-6-ιlkyl, cyano and nitro;
Rc is, independently, at each instance, Cι-6alkyl, Cι-4haloalkyl, phenyl or benzyl; Rd is, independently, at each instance, H, Cι-6alkyl, phenyl, benzyl or a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the Cι-6alkyl , phenyl, benzyl, naphthyl and heterocycle are substituted by 0, 1, 2, 3 or 4 substituents selected from Cι-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro, Rb, -C(=O)Rc, -ORb, -NRaRa, -NRaRb, -C(=O)ORc, -C(=O)NRaRa, -OC(=O)Rc, -NRaC(=O)Rc, -NRaS(=O)mRc and -S(=O)mNRaRa; and m is 1 or 2.
15. A compound or salt according to Claim 1, wherein R1 is phenyl substituted by 2 or 3 substituents selected from Cι-6alkyl, halogen, Cι-4haloalkyl, -Od-6alkyl, cyano and nitro.
16. A compound or salt according to Claim 1, wherein R1 is benzyl substituted by 1, 2 or 3 substituents selected from Cι-6alkyl, halogen, d-4haloalkyl, -OCι-6alkyl, cyano and nitro.
17. A compound or salt according to Claim 1, wherein R1 is naphthyl substituted by 1, 2 or 3 substituents selected from d-6alkyl, halogen, d-4haloalkyl, -Od-ealkyl, cyano and nitro.
18. A compound or salt according to Claim 1, wherein R1 a saturated or unsaturated 5- or 6-membered ring heterocycle containing 1, 2 or 3 atoms selected from N, O and S, with no more than 2 of the atoms selected from O and S, wherein the heterocycle is substituted by 1, 2 or 3 substituents selected from d-6alkyl, halogen, Cι-4haloalkyl, -Od-6alkyl, cyano and nitro.
19. A compound or salt according to Claim 1, wherein one of R3 or R4 is Cι.4haloalkyl or d-8alkyl.
20. A compound or salt according to Claim 1, wherein R5 is, independently, in each instance, Cι-8alkyl, d-4haloarkyl, halogen, -OCι-6alkyl, -NRaRd or NRdC(=O)Rd.
21. A compound or salt according to Claim 1, wherein R6 is not H.
22. A compound or salt according to Claim 1 , wherein R7 is not H.
23. A pharmaceutical composition comprising a compound according to Claim 1 and a pharmaceutically-acceptable diluent or carrier.
24. The use of a compound according to Claim 1 as a medicament.
25. The use of a compound according to Claim 1 in the manufacture of a medicament for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH.
26. The use of a compound according to Claim 1 in the manufacture of a medicament for the treatment of osteoporosis or hyperparathyroidism.
27. A method of using a compound according to Claim 1 for the treatment of diseases associated with bone disorders or associated with excessive secretion of PTH.
28. A method of using a compound according to Claim 1 for the treatment of osteoporosis or hyperparathyroidism.
29. A process for making a compound according to Claim 1 comprising the step of: reacting a compound having the structure
Figure imgf000072_0001
with an amine having the structure
Figure imgf000072_0002
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Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005068433A1 (en) * 2004-01-14 2005-07-28 Novartis Ag Benzimidazole derivatives
WO2005115975A1 (en) * 2004-05-28 2005-12-08 Tanabe Seiyaku Co., Ltd. Arylalkylamines and process for production thereof
WO2006123725A1 (en) 2005-05-19 2006-11-23 Astellas Pharma Inc. Pyrrolidine derivative or salt thereof
WO2007124465A3 (en) * 2006-04-20 2008-04-10 Amgen Inc Stable emulsion formulations
US7361789B1 (en) 2004-07-28 2008-04-22 Amgen Inc. Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis
WO2008121386A2 (en) 2007-03-30 2008-10-09 Amgen Inc. Calcimimetic compounds for use in the treatment of bowel disorders
WO2010104882A1 (en) 2009-03-10 2010-09-16 Amgen Inc. Methods of modulating sperm motility
WO2010136035A2 (en) 2009-05-27 2010-12-02 Leo Pharma A/S Novel calcium sensing receptor modulating compounds and pharmaceutical use thereof
WO2010136037A1 (en) 2009-05-27 2010-12-02 Leo Pharma A/S Novel calcium sensing receptor modulating compounds and pharmaceutical use thereof
WO2012000499A1 (en) 2010-06-30 2012-01-05 Leo Pharma A/S New polymorphic form of a calcimimetic compound
WO2012000498A1 (en) 2010-06-30 2012-01-05 Leo Pharma A/S New polymorphic form of a calcimimetic compound
WO2012069420A2 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Calcium-sensing receptor-active compounds
WO2012069402A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Substituted cyclopentyl - azines as casr- active compounds
WO2012069419A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Calcium-sensing receptor-active compounds
WO2012069421A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Calcium-sensing receptor-active compounds
US10501457B2 (en) 2013-03-14 2019-12-10 Osteoqc Inc. Compounds for bone growth
US10947236B2 (en) 2018-08-14 2021-03-16 Osteoqc Inc. Pyrrolo-dipyridine compounds
US11903949B2 (en) 2018-08-14 2024-02-20 Ossifi Therapeutics Llc Fluoro beta-carboline compounds

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6908935B2 (en) * 2002-05-23 2005-06-21 Amgen Inc. Calcium receptor modulating agents
WO2005065050A2 (en) * 2003-12-25 2005-07-21 Asahi Kasei Pharma Corporation Bicyclic compound
EP1937233B1 (en) * 2005-09-02 2013-01-09 Amgen Inc. Modulating intestinal fluid balance using calcimimetics
WO2007100880A1 (en) * 2006-02-28 2007-09-07 Amgen Inc. Cinnoline and quinazoline derivates as phosphodiesterase 10 inhibitors
AU2007230724B2 (en) * 2006-03-23 2014-01-30 Amgen Inc. Methods and compositions for making and using polymorphs of cinacalcet
WO2009051718A2 (en) * 2007-10-15 2009-04-23 Amgen Inc. Calcium receptor modulating agents
WO2009155527A2 (en) * 2008-06-19 2009-12-23 Progenics Pharmaceuticals, Inc. Phosphatidylinositol 3 kinase inhibitors
IN2015MN00421A (en) * 2012-08-27 2015-09-04 Lupin Ltd
GB201217330D0 (en) 2012-09-28 2012-11-14 Univ Cardiff Therapeutic for treating inflammatory lung disorders

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996012697A2 (en) * 1994-10-21 1996-05-02 Nps Pharmaceuticals, Inc. Calcium receptor-active compounds
WO1997041090A1 (en) * 1996-05-01 1997-11-06 Nps Pharmaceuticals, Inc. Inorganic ion receptor-active compounds
US6001884A (en) * 1991-08-23 1999-12-14 Nps Pharmaceuticals, Inc. Calcium receptor-active molecules
WO2001090069A1 (en) * 2000-05-24 2001-11-29 Centre National De La Recherche Scientifique (Cnrs) Novel calcium receptor active molecules and method for preparing same
WO2002051805A1 (en) * 2000-12-27 2002-07-04 Bayer Aktiengesellschaft Indole derivatives as ligands of thyroid receptors

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US444946A (en) * 1891-01-20 Method of electric welding
US143212A (en) * 1873-09-23 Improvement in attachments for ladies work-tables
PT72878B (en) 1980-04-24 1983-03-29 Merck & Co Inc Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents
DE69433714T2 (en) 1991-08-23 2005-03-31 NPS Pharmaceuticals, Inc., Salt Lake City CALCIUM - RECEPTOR ACTIVE ARYLALKYLAMINE
US6031003A (en) 1991-08-23 2000-02-29 Nps Pharmaceuticals, Inc. Calcium receptor-active molecules
US6011068A (en) 1991-08-23 2000-01-04 Nps Pharmaceuticals, Inc. Calcium receptor-active molecules
JP2728564B2 (en) 1991-08-23 1998-03-18 エヌピーエス・ファーマシウティカルズ・インコーポレイテッド Calcium receptor activating molecule
KR100296899B1 (en) 1993-02-23 2001-10-24 쉘비 칼베르그 모르스 Calcium receptor active molecule
AU3414295A (en) 1994-08-19 1996-03-14 Nps Pharmaceuticals, Inc. Methods and compounds active at metabotropic glutamate receptors useful for treatment of neurological disorders and diseases
AU3642795A (en) 1994-09-27 1996-04-19 Merck & Co., Inc. Endothelin receptor antagonists for the treatment of emesis
US5585388A (en) 1995-04-07 1996-12-17 Sibia Neurosciences, Inc. Substituted pyridines useful as modulators of acetylcholine receptors
ATE400653T1 (en) 1995-07-26 2008-07-15 Astrazeneca Ab CHIMERIC RECEPTORS AND METHOD FOR IDENTIFYING COMPOUNDS HAVING ACTIVITY AS METABOTROPIC GLUTAMA RECEPTORS AND USE OF SUCH COMPOUNDS IN THE TREATMENT OF NEUROLOGICAL DISEASES AND NEUROLOGICAL DISORDERS
IL126458A (en) 1996-04-09 2004-06-20 Nps Pharma Inc Calcium receptor inhibiting calcilytic compounds
KR100771092B1 (en) 1996-07-08 2007-10-30 기린 파마 가부시끼가이샤 Calcium Receptor-Active Compounds
PT966436E (en) 1997-02-21 2003-03-31 Bayer Ag ARILSULFONAMIDES AND ANALOGS AND THEIR APPLICATION FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES
UY24949A1 (en) 1997-04-08 2001-04-30 Smithkline Beecham Corp CALCILITE COMPOUNDS
WO1999001439A1 (en) 1997-07-03 1999-01-14 Du Pont Pharmaceuticals Company Aryl-and arylamino-substituted heterocycles as corticotropin releasing hormone antagonists
JP2002522532A (en) 1998-08-12 2002-07-23 スミスクライン・ビーチャム・コーポレイション Calcium decomposing compound
CA2347092A1 (en) 1998-10-14 2000-04-20 Ortho-Mcneil Pharmaceutical, Inc. 1,2-disubstituted cyclopropanes
DK1157005T3 (en) 1999-02-24 2005-02-14 Hoffmann La Roche 3-phenylpyridine derivatives and their use as NK-1 receptor antagonists
TR200102490T2 (en) 1999-02-24 2001-12-21 F.Hoffmann-La Roche Ag Phenyl and pyridinyl derivatives
EP1074539B1 (en) 1999-08-04 2007-10-17 Sumitomo Chemical Company, Limited Process for producing optically active 3,3,3,-trifluoro-2-hydroxy-2-methylpropionic acid, and salt thereof
FR2800735B1 (en) 1999-11-09 2002-02-01 Centre Nat Rech Scient NOVEL ARALKYL-1,2-DIAMINES HAVING CALCIMIMETIC ACTIVITY AND THEIR METHOD OF PREPARATION
ES2254077T3 (en) 1999-12-18 2006-06-16 Wella Aktiengesellschaft DERIVATIVES 2-AMINOALQUIL-1,4-DIAMINOBENCENO AND ITS USE FOR DYING FIBERS.
DE10028402A1 (en) 2000-06-13 2001-12-20 Merck Patent Gmbh New pyridinylamino-alkanoyl-glycyl-beta-alanine derivatives, are integrin inhibitors useful for treating, e.g. thrombosis, cardiac infarction, coronary heart disease, inflammation, tumors, osteoporosis or restenosis
US6900232B2 (en) 2000-06-15 2005-05-31 Pharmacia Corporation Cycloalkyl alkanoic acids as integrin receptor antagonists
CA2448160A1 (en) * 2001-05-25 2002-12-05 Queen's University At Kingston Heterocyclic beta-amino acids and their use as anti-epileptogenic agents

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6001884A (en) * 1991-08-23 1999-12-14 Nps Pharmaceuticals, Inc. Calcium receptor-active molecules
WO1996012697A2 (en) * 1994-10-21 1996-05-02 Nps Pharmaceuticals, Inc. Calcium receptor-active compounds
WO1997041090A1 (en) * 1996-05-01 1997-11-06 Nps Pharmaceuticals, Inc. Inorganic ion receptor-active compounds
WO2001090069A1 (en) * 2000-05-24 2001-11-29 Centre National De La Recherche Scientifique (Cnrs) Novel calcium receptor active molecules and method for preparing same
WO2002051805A1 (en) * 2000-12-27 2002-07-04 Bayer Aktiengesellschaft Indole derivatives as ligands of thyroid receptors

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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US8030497B2 (en) 2004-01-14 2011-10-04 Novartis Ag Benzimidazole derivatives
US8492111B2 (en) 2004-05-28 2013-07-23 Mitsubishi Tanabe Pharma Corporation Arylalkylamine compound and process for preparing the same
US8362274B2 (en) 2004-05-28 2013-01-29 Mitsubishi Tanabe Pharma Corporation Arylalkylamine compound and process for preparing the same
US8759387B2 (en) 2004-05-28 2014-06-24 Mitsubishi Tanabe Pharma Corporation Arylalkylamine compound and process for preparing the same
US8778628B2 (en) 2004-05-28 2014-07-15 Mitsubishi Tanabe Pharma Corporation Arylalkylamine compound and process for preparing the same
US8703721B2 (en) 2004-05-28 2014-04-22 Mitsubishi Tanabe Pharma Corporation Arylalkylamine compound and process for preparing the same
WO2005115975A1 (en) * 2004-05-28 2005-12-08 Tanabe Seiyaku Co., Ltd. Arylalkylamines and process for production thereof
US7361789B1 (en) 2004-07-28 2008-04-22 Amgen Inc. Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis
EP1882684A1 (en) * 2005-05-19 2008-01-30 Astellas Pharma Inc. Pyrrolidine derivative or salt thereof
JPWO2006123725A1 (en) * 2005-05-19 2008-12-25 アステラス製薬株式会社 Pyrrolidine derivative or its salt
EP1882684A4 (en) * 2005-05-19 2009-12-30 Astellas Pharma Inc Pyrrolidine derivative or salt thereof
WO2006123725A1 (en) 2005-05-19 2006-11-23 Astellas Pharma Inc. Pyrrolidine derivative or salt thereof
JP4573133B2 (en) * 2005-05-19 2010-11-04 アステラス製薬株式会社 Pyrrolidine derivative or its salt
CN101175724B (en) * 2005-05-19 2011-12-07 安斯泰来制药有限公司 pyrrolidine derivative or salt thereof
WO2007124465A3 (en) * 2006-04-20 2008-04-10 Amgen Inc Stable emulsion formulations
US8779004B2 (en) 2006-04-20 2014-07-15 Amgen, Inc. Stable emulsion formulations
WO2008121386A2 (en) 2007-03-30 2008-10-09 Amgen Inc. Calcimimetic compounds for use in the treatment of bowel disorders
WO2010104882A1 (en) 2009-03-10 2010-09-16 Amgen Inc. Methods of modulating sperm motility
US8765676B2 (en) 2009-05-27 2014-07-01 Leo Pharma A/S Calcium sensing receptor modulating compounds and pharmaceutical use thereof
US8785494B2 (en) 2009-05-27 2014-07-22 Leo-Pharma A/S Calcium sensing receptor modulating compounds and pharmaceutical use thereof
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WO2010136037A1 (en) 2009-05-27 2010-12-02 Leo Pharma A/S Novel calcium sensing receptor modulating compounds and pharmaceutical use thereof
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WO2012000499A1 (en) 2010-06-30 2012-01-05 Leo Pharma A/S New polymorphic form of a calcimimetic compound
US8946474B2 (en) 2010-06-30 2015-02-03 Leo Pharma A/S Polymorphic form of a calcimimetic compound
US9056814B2 (en) 2010-06-30 2015-06-16 Leo Pharma A/S Polymorphic form of a calcimimetic compound
WO2012069419A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Calcium-sensing receptor-active compounds
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WO2012069402A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Substituted cyclopentyl - azines as casr- active compounds
WO2012069421A1 (en) 2010-11-26 2012-05-31 Leo Pharma A/S Calcium-sensing receptor-active compounds
US10501457B2 (en) 2013-03-14 2019-12-10 Osteoqc Inc. Compounds for bone growth
US11267814B2 (en) 2013-03-14 2022-03-08 OsteoQC, Inc. Compounds for bone growth
US10947236B2 (en) 2018-08-14 2021-03-16 Osteoqc Inc. Pyrrolo-dipyridine compounds
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US11903949B2 (en) 2018-08-14 2024-02-20 Ossifi Therapeutics Llc Fluoro beta-carboline compounds

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AR040095A1 (en) 2005-03-16

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