Therapeutic agent for pain

Abstract

[Problem] Provided is a pharmaceutical, in particular, a pharmaceutical composition which is useful for the treatment of pain. [Means for Solution] The present inventors have made extensive studies using model animals with pain for the purpose of providing a therapeutic agent for pain. As a result, they have found that 11β-hydroxydehydrogenase type 1 (11β-HSD1) inhibitor, in particular, a triazole compound having a cyclic group at the 3-position (or 5-position) of a triazole ring has a good effect of ameliorating chronic pain. That is, according to the present invention, a pharmaceutical composition comprising an 11β-HSD1 inhibitor, in particular, the triazole compound of the present invention, as an active ingredient, is useful for the treatment of pain (particularly, neuropathic pain or fibromyalgia).

Claims

1. A method for treating neuropathic pain, comprising administering, to a subject in need thereof, an effective amount of a compound selected from the group consisting of: 3-(2-chloro-4-fluorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole, 3-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazole, 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-ethyl-4H-1,2,4-triazol-3-yl}benzamide, 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-methyl-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide, 4-{4-cyclopropyl-5-[1-(2,4-difluorophenoxy)-1-methylethyl]-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide, and 3-fluoro-4-{4-isopropyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide, or a pharmaceutically acceptable salt thereof, wherein said compound is administered at a daily dose of 0.001 to 100 mg/kg body weight.

2. The method according to claim 1, wherein said compound is 3-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazole or a pharmaceutically acceptable salt thereof.

3. The method according to claim 1, wherein said compound is 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-methyl-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide or a pharmaceutically acceptable salt thereof.

4. The method according to claim 1, wherein said compound is 4-{4-cyclopropyl-5-[1-(2,4-difluorophenoxy)-1-methylethyl]-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide or a pharmaceutically acceptable salt thereof.

5. The method according to claim 1, wherein said compound is 3-(2-chloro-4-fluorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole or a pharmaceutically acceptable salt thereof.

6. The method according to claim 1, wherein said compound is 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-ethyl-4H-1,2,4-triazol-3-yl}benzamide or a pharmaceutically acceptable salt thereof.

7. The method according to claim 1, wherein said compound is 3-fluoro-4-{4-isopropyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide or a pharmaceutically acceptable salt thereof.

8. The method according to claim 1, wherein said compound is administered at a daily dose of 0.001 to 10 mg/kg body weight.

9. The method according to claim 1, wherein said compound is administered at a daily dose of 0.1 to 10 mg/kg body weight.

Description

EMBODIMENTS FOR CARRYING OUT THE INVENTION

(1) Hereinafter, the present invention will be described in detail.

(2) The “lower alkyl” is preferably linear or branched alkyl having 1 to 6 carbon atoms (hereinafter abbreviated as C.sub.1-6), specifically methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, or the like, more preferably C.sub.1-4 alkyl, and particularly preferably methyl, ethyl, n-propyl, or isopropyl.

(3) The “lower alkylene” is preferably linear or branched C.sub.1-6 alkylene, specifically, methylene, ethylene, trimethylene, tetramethylene, pentamethylene, hexamethylene, propylene, methylmethylene, ethylethylene, 1,2-dimethylethylene, 1,1,2,2-tetramethylethylene, or the like, more preferably, C.sub.1-4 alkylene, and particularly preferably methylene, ethylene, or trimethylene.

(4) The “halogen” means F, Cl, Br, or I.

(5) The “halogeno-lower alkyl” is lower alkyl substituted with one or more halogen atoms, preferably lower alkyl substituted with 1 to 7 halogen atoms, more preferably lower alkyl substituted with 1 to 5 halogen atoms, and still more preferably fluoromethyl, difluoromethyl, or trifluoromethyl.

(6) The “halogeno-lower alkylene” is lower alkylene substituted with one or more halogen atoms, preferably lower alkylene substituted with 1 to 7 halogen atoms, and more preferably fluoromethylene, difluoromethylene, trifluoromethylmethylene, or bistrifluoromethylmethylene.

(7) The “cycloalkyl” is a C.sub.3-10 saturated hydrocarbon ring group, which may have a bridge, specifically, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, adamantyl, or the like, preferably C.sub.3-8 cycloalkyl, and more preferably cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.

(8) The “cycloalkenyl” is C.sub.3-15 cycloalkenyl, which may have a bridge and includes a cyclic group fused with a benzene ring in a moiety with a double bond, specifically, a cyclopentenyl, cyclopentadienyl, cyclohexenyl, cyclohexadienyl, 1-tetrahydronaphthyl, 1-indenyl, 9-fluorenyl, or the like, more preferably C.sub.5-10 cycloalkenyl, and particularly preferably cyclopentenyl or cyclohexenyl.

(9) The “aryl” is a C.sub.6-14 monocyclic to tricyclic aromatic hydrocarbon ring group, preferably phenyl or naphthyl, and more preferably phenyl.

(10) The “heterocyclic” group means a cyclic group of i) a monocyclic 3- to 8-membered (preferably 5- to 7-membered) heterocycle having 1 to 4 hetero atoms selected from O, S, and N, or ii) a bicyclic 8- to 14-membered (preferably 9- to 11-membered) heterocycle or a tricyclic 11- to 20-membered (preferably 12- to 15-membered) heterocycle having 1 to 5 hetero atoms selected from O, S, and N, which is formed by the ring fusion of the monocyclic heterocycle with one or two rings selected from the group consisting of a monocyclic heterocycle, a benzene ring, a C.sub.5-8 cycloalkane, and a C.sub.5-8 cycloalkene. The ring atom, S or N, may be oxidized to form an oxide or a dioxide. The “heterocyclic” group is preferably aziridinyl, azetidyl, pyrrolidinyl, piperidinyl, piperazinyl, homopiperazinyl, oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, morpholinyl, homomorpholinyl, tetrahydrothiopyranyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyrazinyl, furyl, thienyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, indolyl, isoindolinyl, indazolyl, indolizinyl, benzimidazolyl, imidazo[1,2-a]pyridinyl, quinoxalinyl, quinolyl, isoquinolyl, quinazolyl, cinnonyl, phthalazyl, benzofuranyl, benzothienyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, 4,5,6,7-tetrahydroindazolyl, 4,5,6,7-tetrahydropyrazolo[4,3-c]pyridinyl, 4,5,6,7-tetrahydrobenzimidazolyl, carbazolyl, or quinuclidinyl, more preferably a monocyclic heterocyclic group, and still more preferably pyrrolidinyl, piperidinyl, piperadinyl, morpholinyl, pyridyl, pyrimidinyl, oxazolyl, isoxazolyl, oxadiazolyl, or thiazolyl.

(11) The “heteroaryl” means an aromatic heterocyclic ring among the “heterocyclic” groups above, specifically, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyrazinyl, furyl, thienyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, indolyl, indazolyl, benzimidazolyl, imidazo[1,2-a]pyridinyl, quinoxalinyl, quinolyl, isoquinolyl, quinazolyl, cinnonyl, phthalazyl, benzofuranyl, benzothienyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, or carbazolyl, and preferably monocyclic heteroaryl, more preferably pyridyl, furyl, thienyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, or thiadiazolyl.

(12) The expression “which may be substituted” means “unsubstituted” or “having 1 to 5 substituents which may be the same as or different from one another”. The term “substituted” means “having 1 to 5 substituents which may be the same as or different from one another”. In addition, in a case where a plurality of substituents is present, the substituents may be the same as or different from one another.

(13) The substituent in the “aryl” and the “heterocyclic group”, each of which may be substituted, in R.sup.1a is preferably a group selected from the following Group G.sup.1 (in which R.sup.0 means —H or lower alkyl; and the same shall apply hereinafter), and more preferably halogen, lower alkyl, halogeno-lower alkyl, —O-lower alkyl, —O-halogeno-lower alkyl, —C(O)NH.sub.2 or heteroaryl, and still more preferably halogen, halogeno-lower alkyl, or —C(O)NH.sub.2.

(14) Group G.sup.1: halogen, cyano, lower alkyl, halogeno-lower alkyl, lower alkylene-OR.sup.0, lower alkylene-N(R.sup.0).sub.2, lower alkylene-N(R.sup.0)C(O)R.sup.0, lower alkylene-N(R.sup.0)S(O).sub.2-lower alkyl, —OR.sup.0, —O-halogeno-lower alkyl, —O-cycloalkyl, —O-aryl, —O-heterocyclic group, —C(O)R.sup.0, —CO.sub.2R.sup.0, —C(O)NH.sub.2, —C(O)N(R.sup.0)-(lower alkyl which may be substituted with —OR.sup.0 or —CO.sub.2R.sup.0), —C(O)N(R.sup.0)-lower alkylene-OR.sup.0, —C(O)N(R.sup.0)-lower)alkylene-N(R.sup.0).sub.2, —C(O)N(R.sup.0)-lower alkylene-S-lower alkyl, —C(O)N(R.sup.0)-lower alkylene-S(O)-lower alkyl, —C(O)N(R.sup.0)-lower alkylene-S(O).sub.2-lower alkyl, —C(O)N(R.sup.0)-lower alkylene-C(O)N(R.sup.0).sub.2, —C(O)N(R.sup.0)-lower alkylene-C(O)N(R.sup.0)-cycloalkyl, —C(O)N(R.sup.0)-lower alkylene-heterocyclic group, —C(O)N(R.sup.0)-cycloalkyl, —C(O)N(R.sup.0)-heterocyclic group, —C(O)N(R.sup.0)N(R.sup.0).sub.2, —C(O)N(R.sup.0)N(R.sup.0)C(O)R.sup.0, —C(O)N(R.sup.0)S(O).sub.2-lower alkyl, —C(O)-heterocyclic group, —C(═NOR.sup.0)—N(R.sup.0).sub.2, —S-lower alkyl, —S(O)-lower alkyl, —S(O).sub.2-lower alkyl, oxo, and a heterocyclic group.

(15) In this case, the aryl and the heterocyclic group in Group G.sup.1 may be substituted with a group selected from the following Group G.sup.2.

(16) Group G.sup.2: halogen, cyano, lower alkyl, halogeno-lower alkyl, —OR.sup.0, —O-halogeno-lower alkyl, —CO.sub.2R.sup.0, —C(O)N(R.sup.0).sub.2, —C(O)N(R.sup.0)S(O).sub.2-lower alkyl, —C(O)N(R.sup.0)S(O).sub.2N(R.sup.0).sub.2, cycloalkyl, and a heterocyclic group.

(17) The substituent in the “aryl”, “heterocyclic group”, and “cycloalkyl”, each of which may be substituted, in Ring A is preferably a group selected from the following Group G.sup.3, more preferably halogen, lower alkyl, halogeno-lower alkyl, —O-lower alkyl, —O-halogeno-lower alkyl, or —C(O)NH.sub.2, and still more preferably halogen, halogeno-lower alkyl, or —C(O)NH.sub.2.

(18) Group G.sup.3: halogen, cyano, lower alkyl, halogeno-lower alkyl, lower alkylene-OR.sup.0, halogeno-lower alkylene-OR.sup.0, lower alkylene-N(R.sup.0).sub.2, lower alkylene-aryl, —OR.sup.0, —O-halogeno-lower alkyl, —O-lower alkylene-OR.sup.0, —O-lower alkylene-N(R.sup.0).sub.2, —O-lower alkylene-CO.sub.2R.sup.0, —O-lower alkylene-C(O)N(R.sup.0).sub.2, —O-lower alkylene-aryl, —O-aryl, —C(O)R.sup.0, —CO.sub.2R.sup.0, —CON(R.sup.0).sub.2, —CON(R.sup.0)-lower alkylene-OR.sup.0, —N(R.sup.0).sub.2, —N(R.sup.0)C(O)R.sup.0, —S-lower alkyl, —S(O)-lower alkyl, —S(O).sub.2-lower alkyl, —S(O).sub.2-aryl, oxo, cycloalkyl, aryl, and a heterocyclic group.

(19) In this case, the aryl and heterocyclic group in Group G.sup.3 may be substituted with halogen, lower alkyl, halogeno-lower alkyl, —OR.sup.0, —O-halogeno-lower alkyl, —CO.sub.2R.sup.0, or —CON(R.sup.0).sub.2.

(20) The substituent in the “aryl” which may be substituted in R.sup.1b is preferably halogen, lower alkyl, halogeno-lower alkyl, —O-lower alkyl, or —O-halogeno-lower alkyl, and more preferably halogen.

(21) The substituent in the “aryl” and the “heteroaryl”, each of which may be substituted, in Ring A.sup.b is preferably halogen, lower alkyl, halogeno-lower alkyl, —O-lower alkyl, —O-halogeno-lower alkyl or —C(O)NH.sub.2, and still more preferably halogen, halogeno-lower alkyl, or —C(O)NH.sub.2.

(22) The “11β-HSD1 inhibitor” is a compound inhibiting the enzyme activity of an 11β-HSD1, and not particularly limited as long as it is effective for pains. Preferably, the 11β-HSD1 inhibitor is a compound having an IC.sub.50 value of 10 μM or less, more preferably 3 μM or less, and still more preferably 1 μM or less in the measurement test on the rat 11β-HSD1 inhibitory activity according to the test method described in Example 1 described later.

(23) The “pain” is preferably neuropathic pain. Further, in other embodiments, it is preferably fibromyalgia.

(24) Preferred embodiments of the compound represented by the formula (I-a), which is an active ingredient for the pharmaceutical of the present invention, are shown below.

(25) (1) A compound represented by the formula (I-b):

(26) ##STR00013## [the symbols in the formula denote the following meanings: R.sup.1b: aryl which may be substituted, R.sup.2b: lower alkyl, R.sup.3b: lower alkyl, R.sup.4b: lower alkyl or cycloalkyl, Ring A.sup.b: aryl or heteroaryl, each of which may be substituted, and the other symbols have the same meanings].

(27) (2) A compound represented by the formula (I-c):

(28) ##STR00014## [the symbols in the formula denote the following meanings: R.sup.1c: phenyl substituted with halogen, R.sup.4c: methyl, ethyl, isopropyl, or cyclopropyl, and Ring A.sup.c: phenyl substituted with halogen or —C(O)NH.sub.2].

(29) (3) The compound as set forth in (2), wherein Ring A.sup.c is phenyl, which is substituted with —C(O)NH.sub.2 at the 4-position and may be further substituted with halogen.

(30) (4) The compound as set forth in (2), wherein Ring A.sup.c is phenyl substituted with halogen.

(31) (5) A compound selected from the group consisting of: 3-(2-bromo-4-fluorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole, 3-(2-chloro-4-fluorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole, 3-(2-chlorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole, 3-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazole, 3-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-5-(2-chloro-4-fluorophenyl)-4-methyl-4H-1,2,4-triazole, 3-(2-fluorophenyl)-4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazole, 4-methyl-3-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-5-[3-(trifluoromethyl)-1H-pyrazol-4-yl]-4H-1,2,4-triazole, 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-ethyl-4H-1,2,4-triazol-3-yl}benzamide, 4-{4-isopropyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide, 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-methyl-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide, 4-{4-cyclopropyl-5-[1-(2,4-difluorophenoxy)-1-methylethyl]-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide, 3-fluoro-4-{4-methyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide, 4-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-isopropyl-4H-1,2,4-triazol-3-yl}benzamide, 3-chloro-4-{4-cyclopropyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide, and 3-fluoro-4-{4-isopropyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}benzamide.

(32) Other preferred embodiments of the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention are shown below.

(33) (a) R.sup.1a is preferably aryl which may be substituted, more preferably phenyl which may be substituted, still more preferably phenyl substituted with halogen, and even still more preferably phenyl substituted with halogens at the 2- and 4-positions, or phenyl substituted with halogens at the 2-, 4-, and 6-positions.

(34) (b) R.sup.2a is preferably lower alkyl, and more preferably methyl.

(35) (c) R.sup.3a is preferably lower alkyl, and more preferably methyl.

(36) (d) R.sup.4 is preferably lower alkyl or cycloalkyl, and more preferably methyl, ethyl, isopropyl, or cyclopropyl.

(37) (e) Ring A is preferably aryl or heteroaryl, each of which may be substituted, more preferably aryl which may be substituted, still more preferably phenyl which may be substituted, even still more preferably phenyl substituted with halogen or —C(O)NH.sub.2, even still more preferably phenyl substituted with halogen, particularly preferably phenyl substituted with halogen at the 2-position, or phenyl substituted with halogens at the 2- and 4-positions. In another embodiment, Ring A is preferably phenyl which is substituted with —C(O)NH.sub.2 and may be further substituted with halogen, more preferably phenyl which is substituted with —C(O)NH.sub.2 at the 4-position and may be further substituted with halogen. Further, in a further embodiment, Ring A is preferably phenyl or pyrrole, each of which is substituted with a group selected from halogen, halogeno-lower alkyl, and —C(O)NH.sub.2.

(38) (f) The compound formed by two or more combination of the groups described in (a) to (e) above.

(39) The compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention may exist in the form of tautomers or geometrical isomers depending on the kind of substituents. In the present specification, the compound of the formula (I-a) shall be described in only one form of isomer, but the active ingredient for the pharmaceutical of the present invention includes other isomers, isolated forms of the isomers, or a mixture thereof.

(40) In addition, the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention may have asymmetric carbon atoms or axial chirality in some cases, and correspondingly, it may exist in the form of optical isomers. The active ingredient for the pharmaceutical of the present invention includes both an isolated form of the optical isomers or a mixture thereof.

(41) Furthermore, the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention also includes a pharmaceutically acceptable prodrug thereof. The pharmaceutically acceptable prodrug is a compound having a group that can be converted into an amino group, a hydroxyl group, a carboxyl group, or the like through solvolysis or under physiological conditions. Examples of the group forming the prodrug include the groups described in Prog. Med., 5, 2157-2161 (1985) and “Iyakuhin no Kaihatsu (Pharmaceutical Research and Development)” (Hirokawa Publishing Company, 1990), Vol. 7, Bunshi Sekkei (Molecular Design), 163-198.

(42) Moreover, the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention may form an acid addition salt or a salt with a base depending on the kind of substituents. Specific examples thereof include acid addition salts with inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, phosphoric acid, and the like, and with organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, mandelic acid, tartaric acid, dibenzoyltartaric acid, ditoluoyltartaric acid, citric acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, aspartic acid, glutamic acid, and the like, and salts with inorganic bases such as sodium, potassium, magnesium, calcium, aluminum, and the like, or organic bases such as methylamine, ethylamine, ethanolamine, lysine, ornithine, and the like, salts with various amino acids or amino acid derivatives such as acetylleucine and the like, ammonium salts, etc.

(43) Moreover, the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention also includes various hydrates or solvates, and crystal polymorphs. In addition, the compound of the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention also includes compounds labeled with various radioactive or non-radioactive isotopes.

(44) (Preparation Methods)

(45) The compound of the formula (I-a) and a salt thereof, which are active ingredients for the pharmaceutical of the present invention, can be prepared using the characteristics based on the basic structure or the type of substituent and by applying various known synthesis methods. During the preparation, replacement of the relevant functional group with a suitable protective group (a group that can be easily converted into the relevant functional group) at the stage from starting material to an intermediate may be effective depending on the type of the functional group in the production technology in some cases. The protective group for such a functional group may include, for example, the protective groups described in “Greene's Protective Groups in Organic Synthesis (4.sup.th Ed, 2006)” written by P. G. M. Wuts and T. W. Greene, and one of these should only be selected and used as necessary depending on reaction conditions. In such a method, a desired compound can be obtained by introducing the protective group, by carrying out a reaction and by eliminating the protective group as necessary.

(46) In addition, the prodrug of the compound of the formula (I-a) can be produced by introducing a specific group at the stage from a starting material to an intermediate or by carrying out the reaction using the obtained compound of the formula (I-a), just as in the case of the above-mentioned protective group. The reaction can be carried out using methods known to those skilled in the art, such as ordinary esterification, amidation, dehydration, and the like.

(47) Hereinbelow, typical preparation methods for the compound of the formula (I-a) will be described. Each of the production processes may also be carried out with reference to the References appended in the present description. Further, the preparation methods of the present invention are not limited to the examples shown below.

(48) (Preparation Process 1)

(49) ##STR00015##

(50) (In the formula, L.sup.1 represents a leaving group. The same shall apply hereinafter.)

(51) The present production process is a method for preparing the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention by cyclization of a compound (1) with a compound (2). Examples of the leaving group of L.sup.1 include chloro, bromo, methoxy, methylsulfanyl, and the like. The reaction can be carried out in a solvent, for example, such as ethers such as tetrahydrofuran (THF), 1,4-dioxane, diglyme, and the like; alcohols such as methanol, ethanol, propanol, butanol, and the like; aprotic polar solvents such as N,N-dimethylformamide (DMF), N-methylpyrrolidin-2-one (NMP), dimethylimidazolidinone, dimethylacetamide (DMA), dimethylsulfoxide (DMSO), and the like; aromatic hydrocarbons such as benzene, toluene, xylene, and the like; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and the like; etc., at room temperature or under heating conditions. Depending on the compound, it may be advantageous in some cases to carry out the reaction in the presence of an acid, for example, an organic acid such as acetic acid, p-toluenesulfonic acid, and the like; a mineral acid such as sulfuric acid, hydrochloric acid, and the like; etc., or in the presence of an organic base such as triethylamine, N,N-diisopropylethylamine, and the like; or an inorganic base such as sodium hydrogen carbonate, potassium carbonate, and the like. Depending on the compound, it may be advantageous in some cases to carry out the reaction in the presence of a phase transfer catalyst such as tetra-n-butylammonium iodide and the like.

(52) (Preparation Process 2)

(53) ##STR00016##

(54) The present preparation process is a method for obtaining the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention by reacting a compound (3) with a compound (4).

(55) The reaction can be carried out using the compound (3) and the compound (4) in equivalent amounts, or with either thereof in an excess amount in a solvent inert to the reaction, for example, alcohols, aromatic hydrocarbons such as benzene, toluene, xylene, and the like, acetic acid, or the like, or in the absence of a solvent, under room temperature to heating, preferably under heating. Depending on the compound, it may be advantageous in some cases to carry out the reaction in the presence of an acid, for example, an organic acid such as acetic acid, p-toluenesulfonic acid, trifluoroacetic acid, and the like; a mineral acid such as sulfuric acid, hydrochloric acid, and the like; etc. Also, it is advantageous in some cases to carry out the reaction using a microwave.

(56) (Preparation Process 3)

(57) ##STR00017##

(58) (In the formula, R.sup.1z is aryl or heteroaryl, each of which may be substituted, and L.sup.2 represents a leaving group. The same shall apply hereinafter.)

(59) The present preparation process is a method for obtaining the compound (I-a-1) which is an active ingredient for the pharmaceutical of the present invention, by O-arylation of a compound (5). Examples of the leaving group of L.sup.2 include halogen such as fluoro, chloro, bromo and the like.

(60) The arylation reaction can be carried out using a compound (5) and a compound (6) in equivalent amounts, or with either thereof in an excess amount, under cooling to heating with refluxing, in the presence of a base, in a solvent inert to the reaction, such as an aprotic polar solvent such as DMF, DMSO, and the like; ethers; etc. Examples of the base include sodium hydride, potassium hydride, butyl lithium, potassium carbonate and the like.

(61) (Preparation Process 4)

(62) ##STR00018##

(63) The present preparation process is a method for preparing the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention by cyclization reaction of a compound (7) with a compound (8).

(64) The cyclization reaction can be carried out in the same manner as in the Production Process 1.

(65) (Preparation Process 5)

(66) ##STR00019##

(67) The present preparation process is a method for obtaining the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention by cyclization of a compound (9).

(68) The cyclization reaction can be carried out in a solvent such as ethers, aromatic hydrocarbons, halogenated hydrocarbons, and the like, at room temperature or under heating conditions. Depending on the compound, it may be advantageous in some cases for the progress of the reaction that the reaction is carried out in the presence of an acid such as an organic acid such as acetic acid, p-toluenesulfonic acid, and the like, or a mineral acid such as sulfuric acid, hydrochloric acid, and the like, etc.

(69) Furthermore, several compounds represented by the formula (I-a) can also be prepared from the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention obtained as above by optionally combining processes commonly adoptable by those skilled in the art, such as known alkylation, acylation, substitution reaction, oxidation, reduction, hydrolysis, and the like.

(70) The starting materials for use in the preparation of the compound (I-a) which is an active ingredient for the pharmaceutical of the present invention can be prepared by applying the methods described below, the methods described in Preparation Examples to be mentioned below, known methods or methods obvious to those skilled in the art, or modified methods thereof.

(71) (Starting Material Synthesis 1)

(72) ##STR00020##

(73) (In the formula, L.sup.3 represents a leaving group. The same shall apply hereinafter.)

(74) The compound (3) can be prepared by cyclization of compound (11) obtained by amidation of the compound (1) and a compound (10). Here, examples of the leaving group of L.sup.3 include chloro, bromo, hydroxy, and the like.

(75) The amidation reaction can be carried out using the compound (1) and the compound (10) in equivalent amounts, or with either thereof in an excess amount, in a solvent such as halogenated hydrocarbons, aprotic polar solvents, and the like, under room temperature to heating conditions. Depending on the compounds, it is advantageous for the smooth progress of the reaction in some cases to carry out the reaction in the presence of an organic base such as triethylamine, N,N-diisopropylethylamine, pyridine, and the like, or an inorganic base such as potassium carbonate, sodium carbonate, and the like.

(76) In the case where the leaving group of L.sup.3 is hydroxy, it is preferable that the reaction be carried out in the presence of a condensing agent such as 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (WSC), dicyclohexylcarbodiimide (DCC), 1,1′-carbonyldiimidazole (CDI), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate (HBTU), and the like. In addition, it is preferable in some cases that an additive (for example, 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), and the like) is used.

(77) The cyclization reaction can be carried out by reacting the compound (11) with a dehydrating agent such as phosphorus oxychloride, trifluoromethanesulfonic anhydride, a reagent prepared from triphenylphosphine and carbon tetrabromide, and the like in a solvent such as an aprotic polar solvent such as halogenated hydrocarbons and the like. Depending on the compound, it is advantageous for the smooth progress of the reaction in some cases to carry out the reaction in the presence of an organic base such as triethylamine, N,N-diisopropylethylamine, pyridine, and the like, or an inorganic base such as potassium carbonate, sodium carbonate, and the like.

(78) (Starting Material Synthesis 2)

(79) ##STR00021##

(80) The compound (5) can be prepared from a compound (12) and the compound (2) in the same manner as in the Preparation Process 1.

(81) (Starting Material Synthesis 3)

(82) ##STR00022##

(83) (In the formula, R represents lower alkyl and L.sup.4 represents a leaving group. The same shall apply hereinafter.)

(84) In addition, the compound (3) can also be prepared by cyclization of the compound (1) with a compound (13). Here, examples of the leaving group of L.sup.4 include chloro, bromo, and the like.

(85) The reaction can be carried out in the same manner as in the Preparation Process 1.

(86) (Starting Material Synthesis 4)

(87) ##STR00023##

(88) The compound (9) can be prepared by the amidation reaction of a compound (14) and a compound (15).

(89) The amidation reaction can be carried out in the same condition as in the amidation of the first step of the starting material synthesis 1.

(90) The compound of the formula (I-a) is isolated and purified as a free compound or a salt, a hydrate, a solvate, or a crystal polymorph thereof. The salt of the compound of the formula (I-a) can also be prepared using a conventional salt formation reaction.

(91) Isolation and purification are carried out by applying common chemical operations such as extraction, fractional crystallization, various types of fractional chromatography, and the like.

(92) A variety of isomers can be prepared by selecting suitable starting compounds or separated using differences in the physicochemical properties between the isomers. For example, optical isomers are obtained by a general optical resolution method of racemic forms (for example, fractional crystallization in which the racemic form is converted into diastereomer salts with an optically active base or acid, chromatography using a chiral column and the like, and the like), or can also be prepared from suitable starting compounds which are optically active.

(93) A pharmaceutical composition for treating pain of the present invention, including one or two or more kinds of the compound of the formula (I-a) as an active ingredient, can be prepared using excipients that are usually used in the art, that is, excipients for pharmaceutical preparation, carriers for pharmaceutical preparation, and the like, according to the methods usually used.

(94) Administration can be accomplished either by oral administration via tablets, pills, capsules, granules, powders, solutions, and the like, or parenteral administration via injections, such as intraarticular, intravenous, or intramuscular injections, and the like, suppositories, eye drops, eye ointments, transdermal liquid preparations, ointments, transdermal patches, transmucosal liquid preparations, transmucosal patches, inhalers, and the like.

(95) As a solid composition for oral administration, tablets, powders, granules, and the like are used. In such a solid composition, one or two or more kinds of the active ingredient(s) are mixed with at least one inactive excipient. In a conventional method, the composition may contain inactive additives, such as a lubricant, a disintegrating agent, a stabilizer, or a solubilization assisting agent. If necessary, tablets or pills may be coated with sugar or with a film of a gastric or enteric coating substance.

(96) The liquid composition for oral administration includes pharmaceutically acceptable emulsions, solutions, suspensions, syrups, elixirs, or the like, and also includes generally used inert diluents, for example, purified water or ethanol. In addition to the inert diluent, the liquid composition may also include auxiliary agents such as a solubilization assisting agent, a moistening agent, and a suspending agent, sweeteners, flavors, aromatics, and antiseptics.

(97) The injections for parenteral administration include sterile aqueous or non-aqueous solution preparations, suspensions, or emulsions. The aqueous solvent includes, for example, distilled water for injection and physiological saline. Examples of the non-aqueous solvent include alcohols such as ethanol. Such a composition may further include a tonicity agent, an antiseptic, a moistening agent, an emulsifying agent, a dispersing agent, a stabilizing agent, or a solubilizing assisting agent. These are sterilized, for example, by filtration through a bacteria retaining filter, blending of a bactericide, or irradiation. In addition, these can also be used by preparing a sterile solid composition, and dissolving or suspending it in sterile water or a sterile solvent for injection prior to its use.

(98) The agent for external use includes ointments, plasters, creams, jellies, patches, sprays, lotions, eye drops, eye ointments, and the like. The agents include generally used ointment bases, lotion bases, aqueous or non-aqueous liquid preparations, suspensions, emulsions, and the like.

(99) The transmucosal agents such as an inhaler, a transnasal agent, and the like, those in the form of a solid, liquid, or semi-solid state are used, can be prepared in accordance with a conventionally known method. For example, a known excipient, and also a pH adjusting agent, an antiseptic, a surfactant, a lubricant, a stabilizing agent, a thickening agent, or the like may be appropriately added thereto. For their administration, an appropriate device for inhalation or blowing can be used. For example, a compound may be administered alone or as a powder of formulated mixture, or as a solution or suspension in combination with a pharmaceutically acceptable carrier, using a conventionally known device such as a measured administration inhalation device, and the like, or sprayer. A dry powder inhaler or the like may be for single or multiple administration use, and a dry powder or a powder-containing capsule may be used. Alternatively, this may be in a form such as a pressurized aerosol spray which uses an appropriate ejection agent, for example, a suitable gas such as chlorofluoroalkane, carbon dioxide, and the like, or other forms.

(100) Usually, in the case of oral administration, the daily dose is from about 0.001 to 100 mg/kg, preferably from 0.1 to 30 mg/kg, and more preferably from 0.1 to 10 mg/kg, per body weight, administered in one portion or in 2 to 4 divided portions. In the case of intravenous administration, the daily dose is suitably administered from about 0.0001 to 10 mg/kg per body weight, once a day or two or more times a day. In addition, a transmucosal agent is administered at a dose from about 0.001 to 100 mg/kg per body weight, once or plural times a day. The dose is appropriately decided in response to the individual case by taking the symptoms, the age, and the gender, and the like into consideration.

(101) A therapeutic agent for pain including the compound of the formula (I-a) or a pharmaceutically acceptable salt thereof as an active ingredient may be used in combination with other therapeutic agents for pain. Such the combined preparations may be administered simultaneously, or separately and continuously, or at a desired time interval. The preparations to be co-administered may be a blend, or may be prepared individually.

EXAMPLES

(102) Hereinafter, the present invention will be described in detail with reference to Examples, but these do not restrict the scope of the present invention.

Example 1

Measurement Test for Rat 11β-HSD1 Inhibitory Activity

(103) The procedure for measuring the 11β-HSD1-inhibitory activity is as follows. The enzyme reaction and the measurement were carried out using a 384-well plate. The enzyme was prepared in accordance with Journal of Biological Chemistry, 2001, Vol. 276, p. 21343-21350. The reaction was carried out by adding a test compound at various concentrations to a reaction liquid consisting of a 5 mM phosphate buffer (pH 6.6), 200 nM cortisone, 40 μM reduced nicotinamide adenine dinucleotide phosphate (NADPH), and rat recombinant 11β-HSD1, followed by incubating at room temperature for one hour (10 μl/well). The test compound was prepared by dissolving in dimethyl sulfoxide (DMSO) such that a DMSO concentration reached 1% in the reaction liquid. After the enzyme reaction was completed, the enzyme inhibitory action was measured by detecting cortisol using a homogeneous time-resolved fluorescence (HTRF) method. Each of a d2-labeled cortisol containing 400 μM carbenoxolone and a cryptate-labeled cortisol antibody (CIS Bio International Co., Ltd.) was added at 5 μl/well, followed by incubating at room temperature for 2 hours, and then the fluorescence intensity was measured using a fluorophotometer (trade name: ARVO HTS 1420, Perkin Elmer/Wallac), and the enzyme inhibitory activity was calculated from the fluorescence intensity ratio of two wavelengths (665 nm/620 nm).

(104) The measurement results were calculated by averaging the values of 3 wells of the same condition. The ratio when DMSO was added instead of the test compound was taken as 0% and the ratio when 11β-HSD1 was not added was taken as 100%, thereby calculating the 50% inhibition concentration of the test compound as IC.sub.50 of the compound inhibitory activity.

(105) The IC.sub.50 values of the typical compounds with respect to the active ingredients for the pharmaceutical of the present invention are shown in Table 1 below. Further, Cpd represents Compound No. (the same shall apply hereinafter).

(106) TABLE-US-00001 TABLE 1 Cpd IC.sub.50 (nM) 1 35 2 52 3 24 4 32 5 263 6 322 7 32 8 70 9 26 10 135 11 64 12 182 13 68 14 16 15 23

Example 2

Test of Spinal Nerve Ligation Model

(107) The test was carried out in accordance with Pain, 1992, Vol. 50, p. 355-363. The lumbar skin and muscle of a rat (SD, male, 5- to 6-week old) were incised under pentobarbital anesthesia and the transverse processes of lumbar L6 were removed to expose lumbar nerves. The L5 and L6 spinal nerves were ligated with silk thread and then the wound was sutured. The treatment was performed on the left side. However, in a case of a pseudo-operation, the wound was sutured without carrying out the nerve ligation.

(108) Drug efficacy evaluation was carried out by a von Frey hair test 7 to 20 days after the operation. The withdrawal response threshold was calculated in accordance with Journal of Neuroscience Methods, 1994, Vol. 53, p. 55-63. The plantar of hindlimb was stimulated using 8 kinds of von Frey filaments (0.41 to 15.14 g), and 50% withdrawal response thresholds were determined by an up-and-down method. The test was initiated from 2.04 g of the filament, and a case where the withdrawal response of the limb was observed was taken as presence of the response.

(109) On the previous day of the drug efficacy evaluation, the animals showing reduction in the thresholds according to a von Frey hair test were preliminarily selected and grouped such that the difference in the average values of the thresholds between the respective groups was reduced.

(110) The test substance was suspended in a 0.5% methylcellulose solution and administered orally 2 hours before the drug efficacy evaluation. The evaluation of the test substance was carried out by determining the improvement rate of the group administered with the test substance when the threshold of the limb on the treatment side in the pseudo-operation animal group was taken as 100% and the threshold of the limb on the treatment side in an operated animal group administered with a solvent was taken as 0%.

(111) The improvement rates of the typical compounds with respect to the active ingredients for the pharmaceuticals of the present invention are shown in Table 2 below.

(112) TABLE-US-00002 TABLE 2 Improvement rate Cpd % (dose) 1 71 (0.3 mg/kg) 2 88 (0.3 mg/kg) 3 62 (0.3 mg/kg) 4 85 (0.3 mg/kg) 5 65 (0.3 mg/kg) 6 52 (0.3 mg/kg) 7 73 (0.3 mg/kg) 8 87 (0.3 mg/kg) 9 78 (0.3 mg/kg) 10 81 (0.3 mg/kg) 11 82 (0.3 mg/kg) 12 54 (0.3 mg/kg) 13 53 (0.3 mg/kg) 14 73 (0.3 mg/kg) 15 86 (0.3 mg/kg)

Example 3

Test of Fibromyalgia Model Induced by Repeated Administration of Reserpine

(113) The test was carried out in accordance with Pain, 2009, Vol. 146, p. 26-33. Rats (SD, male, 7 weeks old) were used.

(114) The threshold measurement for the muscle pressure pain was carried out according to the method of Schafers et al. (Pain, 2003, Vol. 104, p. 579-588). The pressure stimulus gradually increasing up to 250 g was applied to the gastrocnemius muscle of the right hindlimb of the rat. The magnitude of the minimum pressure stimulus at which the rat showed a withdrawal response with respect to pressure stimulus of the right hindlimb was measured as a muscle pressure pain threshold (g). The measurements were carried out in triplicate for each point of time and the average thereof was taken as a measured value.

(115) A solvent (0.5% acetic acid/water) or reserpine at 1 mg/kg was subcutaneously administered on a dorsal subcutaneous part for 3 days once per day. The administration volume of the solvent or reserpine was taken as 1 mL per kg of a body weight of an animal. The muscle pressure pain thresholds of the respective rats were measured at 6 days after the initiation of the administration of the solvent or reserpine, and grouped such that the difference in the average values of the thresholds between the respective groups was reduced.

(116) The drug efficacy evaluation was carried out the next day. The test substance was suspended in a 0.5% methylcellulose solution and the muscle pressure pain thresholds were measured 30, 60, and 120 minutes after oral administration. For the normal rats, drug administration was not carried out, and only the measurement of the muscle pressure pain thresholds was carried out. The measurement of the drug effect was carried out by an experimenter who does not know the drug treatment context to an animal. The evaluation of the test substance was carried out by determining the maximal improvement rate of the group administered with the test substance among at time points of 30, 60, and 120 minutes after the administration when the muscle pressure pain threshold of the normal rat is taken as 100% and the muscle pressure pain threshold of the rat treated with reserpine while administered with the solvent is taken as 0%.

(117) The improvement rates of the typical compounds with respect to the active ingredients for the pharmaceuticals of the present invention are shown in Table 3 below.

(118) TABLE-US-00003 TABLE 3 Maximum improvement Point for Cpd rate % (dose) calculation (min) 2 30 (1 mg/kg) 120 4 82 (1 mg/kg) 30 8 41 (1 mg/kg) 120 10 65 (1 mg/kg) 120 11 83 (1 mg/kg) 30 15 45 (1 mg/kg) 120

(119) As the results of the tests above, it was confirmed that the compound represented by the formula (I-a) is effective in various pain models. Therefore, it is apparent that the compound represented by the formula (I-a) which is an active ingredient for the pharmaceutical of the present invention can be used for the treatment of pain (in particular, neuropathic pain, fibromyalgia, or the like).

(120) The methods for preparing the compounds with respect to the active ingredients for the pharmaceuticals of the present invention are shown below.

(121) All the compounds 1 to 15 described in Tables 4 to 6 below are known compounds and can be prepared in the following manner.

(122) All the compounds 1 to 15 are described as Example compounds in the pamphlet of International Publication WO 2010/001946, and can be prepared by the method described in this publication. For example, the compound 2 is described as Example 65 of this publication.

(123) The following abbreviations are used in Tables below.

(124) Cpd: Compound No., Structure: Structural formula (in the case where HCl is described in the structural formula, it denotes that the compound is hydrochloride salt).

(125) TABLE-US-00004 TABLE 4 Cpd Structure 1 2 3 4 5 6 7 0

(126) TABLE-US-00005 TABLE 5 8 9 10 11 12 13 14

(127) TABLE-US-00006 TABLE 6 15

INDUSTRIAL APPLICABILITY

(128) An 11β-HSD1 inhibitor which is an active ingredient for the pharmaceutical of the present invention, in particular, the compound of the formula (I-a), is useful for the treatment of pain (in particular, neuropathic pain or fibromyalgia).