Title of Invention

ACYLATED AMINOALKYLIMIDAZOLE AND- TRIAZOLE DERIVATIVES

Abstract

The present invention relates to a compound of formula wherein eight R1 represents pheny, naphthy or pyridly, whereby these four substituents are optionally monosubstituted by halogen, alkoxy,alkyl, dialkylamino or cyano and R2 represents hydrogen; or R1 represents hydrogen, halogen,alkoxy, cyano, alkoxycarbonyl, alkylcarbonyl or amino optionally disubstituted by alkyl of1 to 4 carbon atoms; and X represents CH or N;in free from or salt form alkyl, alkox, dialkylamino, alkoxycarbonyl & alkylcarbonyl should al;l be taken to mean that the alkyl/alkoxy part has 1 to 4 carbon atoms.

Full Text

ACYLATED AMINOALKANIMIDAZOLES AND -TRIAZOLES The invention relates to acyiated aminoalkylimidazole and -triazole derivatives. More particularly the invention concerns compounds of formula I wherein either R. represents phenyl, naphthyi, thienyl or pyridyl, whereby these four substituents are optionally mono-substituted by halogen, alkoxy, alkyl, dialkylamino or cyano and R2 represents hydrogen; or R. represents hydrogen and R? represents pyridyl or 2-(5-chloro)pyridyl; R3 represents hydrogen, halogen, alkyl, cyano, alkoxycarbonyl. alkylcarbonyl or optionally substituted amino; and X represents CH or N; in free form or salt form, hereinafter briefly named "the compounds of the invention". n preferably is phenyl. When it i$ other than phenyl \{ preferably is hydrogen. R2 oreferably is hydrogen. R3 preferably is halogen. It preferably is in 4 position. X preferably is CH. When R1 is other than hydrogen ft preferabfy is unsubstituted. When pftenyf te substituted it preferably is substituted in 4 position. When pyridyl is substituted it preferably is substituted in 5 position. Halogen is fluorine, chlorine, bromine or iodine, preferably chlorine. Alkoxy and/or alkyl and/or the alkyl substituents in dialkylamino and/or the aikoxy part in alkoxycarbonyl and/or the alkyl part in alkylcarbonyl preferably are independently of 1 to 4, especially 1 or 2, particularly 1 carbon atom(s). Optionally substituted amino preferably is unsubstituted. When it is substituted it preferably is disubstituted, preferably by alkyl of 1 to 4 carbon atoms. Pyridyl preferably is 2- or 4-pyridyl. Naphthyl preferably is 1-naphthyl. A group of compounds of the invention is the compounds of formula Is wherein either R,s represents phenyl, phenyl monosubstituted by halogen or 1-naphthyl and R2s represents hydrogen; or R1S represents hydrogen and R2s represents pyridyl or 2-(5-chloro)pyridyl; and R3s represents halogen or alkoxy of 1 to 4 carbon atoms; in free form or salt form. In a subgroup of compounds of formula Is R3s chlorine. In a further subgroup R3s is alkoxy of 2 to 4 carbon atoms. In a further subgroup phenyl monosubstituted by halogen is phenyl monosubstituted by nhlorino, preferably in 4 position. !n a further subgroup Rts represents phenyl or, preferably, phenyl monosubstituted by chlorine in 4 position; R2s represents hydrogen; and R3s represents chlorine in 4 position. A further group of compounds of the invention is the compounds of formula Ip wherein either R,p represents phenyl optionally monosubstituted by chlorine in £ position and R2p represents hydrogen or R,p represents hydrogen and R2p represents 2-(5-chloro)pyridyl. and Xp represents CH or N; or R,p represents 1-naphthylr R2p represents hydrogen and Xp represents CH; in free form or pharmacologically acceptable acid addition salt form. The compounds of the invention may be prepared by a process comprising a) acylating corresponding compounds of formula wherein the substituents are as defined above, to introduce a corresponding biphenyl-4-carbonyl group; or b) for the preparation of compounds of formula la wherein R3 and X are as defined above ami fV has the same signiSeanee as R, as defined above but without hydrogen, reacting corresponds compounds of formula wherein R/ and R3 are as defined above, with the corresponding compound of formula wherein X is as defined above; and recovering the resultant compounds of formula I in free-form or salt form. The process of the invention can be effected in conventional manner. Process variant a) may for example be carried out by reacting a compound of formula II with an appropriate acy! halide in a solvent, e.g. in an organic or inorganic base which may at the same time act as an acid binding agent, such as pyridine, optionally with addition of an acylation accelerator such as 4-dimethylaminopyridine. The reaction may also be carried out by reacting a compound of formula II with an appropriate active ester or a further activated acyl derivative, e.g. a mixed anhydride or an imidazotide available by using N,N-carbonyf-diimidazoie as a reagent. The reaction can thus for example be carried out with a 2-pyridyl-thiol ester such as 4'-chlorobiphenyl-4-carboxylic acid-2-pyridyl-thiol ester in an inert solvent such as a di-lower alkyl carboxylic acid amide, e g dimethylformamide, preferably at room temperature. Process variant b) may be carried out by mixing a compound of formula III or Ilia with a compound of formula IV and heating the mixture to elevated temperature, e.g. to about 120°C. The starting materials are either known or may be prepared according to known procedures or analogously to known procedures or analogously as described herein, e.g. in the examples. The compounds of formula II may e.g. be prepared according to the following reaction scheme: In the above reaction scheme R2' has the same significance as R2 as defined above but without hydrogen, Y represents halogen, preferably chlorine, and the other substituents are as defined above. in end products with unchanged configuration when either no reaction step, or two reaction steps are used which invert the configuration at the chirality center. The single steps of these reactions may be carried out in conventional manner. A compound of the invention can be in free form or salt, such as acid addition salt form. A compound of the invention in free form can be converted into a salt, such as an acid addition salt form thereof, e.g. the hydrochloride or the nitrate, in conventional manner and vice-versa. Example 1: 1-(5-Chloro-2-pyridyh-2-(1H-imida2ol-1-vn- N-[4-(4-chlorophenyl)benzoyn-1-aminoethane [process variant a)] To a solution of 0.44 g of 1-amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol- 1-yl)ethane in 1 ml of dimethylformamide is added a solution of 0.645 g of 4'-chlorobiphenyl-4-carboxylic acid-2-pyridyl-thiol ester in 2 ml of dry dimethylformamide. The reaction mixture is stirred at room temperature and under argon for 18 hours. The reaction mixture is poured onto cold saturated brine and extracted with ethyl acetate. The combined organic phases are washed with brine, dried over Na2S04, filtered and the solvent is evaporated (= working up process A). Treatment of the crude product with diethylether gives the title compound as colourless crystals; m.p.: 143-146°. Using optically active enantiomers as starting material and proceeding as described above yields the corresponding optically active enantiomers of the title compound: (+)-enantiomer: [ot]D20 = + 6.7° (c = 0.52, methanol); m.p.: 175-186° (-)-enantiomer: [a]D20 = - 7.0° (c = 0.52, methanol); m.p.: 175-186°. Example 7: N-r4^4-ChtorophenynbenzoylV2-(1 H-imidazoM-y»-2(S)-Dhenvl-t-amtnoethane [process variant a)] The solution of 0,96 g of crude (S)-2-phenyl-2-(1H-imidazol-1ylH-aniinoethan^ :~ 5 ml of N,N-dimethylforrnamide is charged, with stirring, with 1g of 4'-chlor©b^>^nyl-4-carboxylic acid-2-pyridyl-thiol ester. After 6 hours the reaction mixture is quenched by pouring into cold water (0°, 50 ml).The precipitate is extracted with ethyl acetate, the organic phase is washed with brine, dried over magnesium sulfate and evaporated. The crystalline residue is triturated with ethanol, filtered by suction and washed with cold ethanol. Drying of the crystals yields the pure title compound; m.p.: 176-177°; [ The (R)-enantiomer of the title compound is prepared analogously starting from (R)-2-phenyl-2-(1H-imidazol-1-yl)-1-aminoethane; m.p.: 176-179°; [a]D20 = -17.4° (c=1,1f methanol). Example 8: K- [4-(4-CAIorophenYl)benzQylI^ 1-aminoethane Iprocess variant b)] 0.398 g of N-(4'-chlorobiphenyl-4-carbonyI)-2(R)-phenyl«aziridine are mixed with 0.15 got imidazole and heated at 110° for 16 hours. After cooling the solid residue is dissolved in 1.5 m\ of DMF by warming. The solution is poured into ice water. The precipitated solid is coltecSad by section, washed with water and dried. The material is purified by chromatography on slfca gel (toluene/ethanol = 8/1). The title compound is obtained as white crystals; m.p.: 176-179°; [a]D20 = + 19.6° (c = 1.0, methanol); 1H-NMR (DMSO-d6) 5 = 8.82 (t, J = 5.3 Hz; 1H); 7.87-7.84 (m; 3H); 7.78-7.74 (m; 4H); 7.55 (d, J = 8.5 Hz; 2H); 7.41-7.30 (m; 6H); 6.92 (s; 1H); 5.70 (dd, J = 6.0, 9.1 Hz; 1H); 4.16-3.94 (m; 2H). Example 9: N-r4-(4-ChlQrpphenyl)benzQyl]-2-(1H-imW9zol-i-y»)-2(R)-phenyi- 1-aminoethane [process variant b)] 380 mg of 2-(4'-chlorobiphenyl-4-yl)-5(S)-phenyl-4,5-dihydro-oxazole and 775 mg of imidazole are heated at 120° for 23 hours. Ethyl acetate and water are added, the organic layer is washed three times with water, dried over magnesium sulfate and concentrated in vacuo. After addition of toluene the title compound precipitates as colourless crystals; m.p.: 176-179° (recrystallized from toluene); [a]D20 = - 17.4° (c = 1.1, methanol). The 'H-NMR spectrum is identical with the spectrum for the S (+)-enantiomer in example 8. Analogously as described in example 8 the following compounds of formula I are obtained according to process variant b), in racernic form: *The 2(3)-enantiomer of the compound of example 10 is obtained analogously as described in example 9 from the correspond1^ 4.5-dIhydro-GxazoIe; m.p. 197-204°; [a]D20 = +1.1° (c = 0,49, chloroform). Example 12: N-f4-{4-ChlorophenyS)benzoyi]-2-{1H-imidazoM-yl)-2"phenyl- 1-aminoethane [process variant a)] 0.94 g of 2-phenyl-2-(1H-imidazol-1-yl)-1-aminoethane are acylated with 0.17 g of 4'-chlorobiphenyl-4-carboxyiic acid-2-pyridyl-thiol ester analogously as described in example 1. Chromatography on silicagel (dichloromethane/ methanol/ aqueous NH3 / heptane = 7/1/0.1/5) gives the title compound as colourless crystals; m.p.: 209-212°. The starting materials may be prepared in the following manner: A) 1-Amino-1-(5-ch[oro-2-pyridyl)-2-(1H-im8da2ol-1-yl)ethane a) 2-Acetyl-5-chloropyridine To a suspension of 56 g of 2-bromo-5-ch!oropyridine in 560 ml of dry diethylether is added a solution of 179 ml of n-butyllithium (15% solution in hexane) at -78° and under argon at such a rate that the temperature never exceeds -72°. Immediately thereafter the solution of 25.7 ml of N,N-dimethylacetamide in dry THF is added. The mixture is stirred for one hour at the same temperature and thereafter decomposed by careful addition of 100 ml of 3N hydrochloric acid, followed by 100 ml of water with vigorous cooling. Working up by process A (see Example 1) and purification by chromatogrphy over silicagel (toluene/ethyl acetate = 20/1) yields the compound as white needles; m.p.: 58-65°. b) 2«Bromoacety!-5-ch!oropyridine hydrobromide To a solution of 10 g of ?-acetyl-5-chloropyridine in 150 ml of 48% aqueous hvdrohromic acid are added 4 ml of bromine dissolved in 40 ml of hvdrobromic acid with ?.tirrinn drop by drop, at 80°. The mixture is stirred for additionally 3 hours at 80°. Afterwards the solution is evaporated in vacuo. The residue is triturated with acetone, filtered by suction, washed with acetone and dried in vacuo to yiefd yellow crystals of the compound, which is used for the next step without purification. c) 2»[2-(1H-lmidazol-1-yl)acetyi3-5-chioropyridine 15 g of 2-bromoacetyi-5-chioropyridine hydrobromide are dissolved in 50 m! of dry dichloromethane, 9.7 g of imidazole are added and the mixture is stirred for 24 hours at room temperature. Evaporation of the solvent in vacuo and subsequent chromatography of the residue over silicagel (dichloromethane/methanol/heptane = 7/1/4) yield the compound as a cream coloured solid; m.p.: 122-129°. d) 1-(5-Chloro-2-pyridyl)-2-(1H-imida2oM-yl)ethane-1-ol A solution of 7.8 g of 2-[2'-(1H-imida20l-1-yl)acetyl]-5-chloropyridine in 40 ml of methanol is charged at 0°, in portions, with 2.0 g of sodium borohydride. The mixture is stirred for one hour at 0°. For working-up the mixture is decomposed by careful addition of 1N hydrochloric acid at 0°, followed by 1N sodium hydroxide to reach a pH of 9. The solvents are evaporated in vacuo. The residue is stirred with water and dichloromethane, the aqueous phase is extracted twice with dichloromethane and the combined organic extracts are washed with brine, dried and evaporated. The compound is obtained as a cream coloured solid; m.p.: >210° (decomp.)- Purification is possible by chromatography over silicagel. e) 1-Chloro-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane 1 g of 1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane-1-ol is dissolved in 2 ml of toluene, 6 ml of thionyl chloride are added and the reaction.mixture is stirred for 30 minutes at room temperature. The solvent and the thionyl chloride in excess are distilled off, the residue is dissolved in 2N NaOH, extracted with ethyl acetate, dried over Na2S04 and evaporated to yield the compound as a colourless oil. f) l-Azido-1-(5-chioro-?-pyridyl)-2-(1H-imidazol-1-yl)ethane 0.92 g of 1-chloro-(5-chloro-2-pyridyl)-2-(1H-imidazoi-1-yl)ethane are added under argon to a solution of 0.37 g of iithium azide in ? ml of do/ dimethylformamide and the reaction *nixture is stirred at 60° for 18 hours. Working up according to process A (see Exampie 1) gives the substance as a yellowish oil. g) 1-Amino-1-(5"Chloro-2-pyridyl)-2-(1H-irnidazoM-yl)ethane A solution of 0.83 g of 1 -azido-1 -(5-chloro-2-pyridyl)-2-(1 H-imidazol-1 -yl)ethane in 4 ml of dry pyridine is stirred under a H2S-aimosphere for 3 hours The reaction mixture is evaporated, the residue is redissclved in 5 ml of dilute acetic acid (acetic acid / water 1 / 4} and extracted with ethyl acetate. The combined organic phases are evaporated to give the title product as a yellowish oil. Analogously as described above under A) the following starting materials of formula II are obtained as viscous yellowish oils, which are used without further purification (X= CH, Ri= H): E) (S)-2-Phenyl-2-(1H-imidazoM-yl)-1-aminoethane a) (R)-2-Amino-2-phenyl-ethanol-0-suIfate hydrogensulfate A solution of 10.65 g of {R)(-}-2-amino-2-pheny!ethano! in 30 mi of wafer is neutralized with 48% sulfuric acid to methyl red end point (4.2 ml), followed by addition of an equal volume of sulfuric acid. Water is then removed at a rotatory evaporator at 70-90°, finally at 130° bath temperature and 0,1 TOT pressure to constant weight. The mixture gradually solidifies and is ground in a mortar. The material can be used without further purification for the next reaction. b) (R)(-)-2-Phenyl-aziridine 16.2 g of finely ground (R)-2-amino-2-phenyl-ethanol-0~suIfate hydrogensulfate is added in portions to a stirred solution of 2N sodium hydroxide at 0°. The reaction mixture is then heated to 100° for 3 hours. For working up the mixture is cooled to room temperature and extracted four times with ether. The organic phase is washed with brine, dried over magnesium sulfate and evaporated. Distillation of the residue under reduced pressure yields the compound as a colourless oil; b.p.: 46° (0.1 Torr); [ c) (S)-2-Phenyl-2-(1H-imidazoM-yl)-1-aminoethane 1g of (R)(-)-2-phenyl-aziridine and 1.14 g of imidazole are heated at 120° for 24 hours. After cooling the reaction mixture can be used for the acylating step without further purification. An analytical sample can be obtained by chromatography over silicagel; 1H-NMR (CDCI3) 8 = 7.66 (s;1H), 7.41 - 7.31 (m; 3H), 7.24 - 7.18 (m; 2H), 7.11 (t, J=1 Hz; 1H), 7.03(t, J = 1Hz; 1H), 5.17 (m; 1H), 3.43 (m; 2H), 2.60 (s, b; 2H). F) N-(4'-Chlorobiphenyl-4-carbonyl)-2(R)-phenyl-aziridine To a solution of 0.232 g of 4'-chlorobiphenyl-4-carboxylic acid in 3 ml of dry DMF, 0.18 g of N,N'-carbonyl-diimidazole are added with stirring at room temperature under argon atmosphere. After one hour a solution of 0.12 g of phenyl-aziridine in 0.5 ml of dry DMF is added dropwise. The reaction mixture is stirred for 21 hours and thereafter worked up as described in example 1. The compound is obtained as a pale yellow oil and used without purification in the next step. G) 2-(4-Chlorobiphenyl-4-yl)-5(S)-phenyl-4.5-dihydro oxazole a) 2-Amino-1(R)-phenyl-ethano! A solution of 15.8 g of R(-)-phenyloxirane in 150 ml of ethanol is cooled to -60 ° and 75 m! of ammonia are added. The reaction mixture is stirred for 70 hours at room temperature in a closed stainless steel reactor. The solvents are evaporated and 300 ml of water and 60 m! of toluene are added. Separation of the aqueous layer and removpj of the solvent in vacuo yields 14.14 g of a colorless solid which contains 86 % 2-amino-1(R)-phenyl-ethanol, 9 % 2-amino-2-phenyl-ethanol and 5 % 2-(2-hydroxy-2-phenyiethylamino)-1 -phenyl-ethanol (assessed by 1H-NMR). The mixture rs used in the next step without further purification. Chromatography oversilicagel(dichloromethane /methanol / 28% aqueous ammonium hydroxyde = 100/10/1} provides an analytical sample; m.p.: 64.6° (sublimes); [a]D20 = - 44.3° (c = 2, ethanol); 1H-NMR (DMSO-ds) 8 = 7.37-7.22 (m; 5H); 4 44 (66, J = 4.4S 7.7 Hz; 1H); 2.70/ 2.57 (ABX, J ^ 11.3, 4.4, 7.7 Hz; 2H); 2.60 (bs; 3H). b) 4'-Chlorobiphenyl-4-carbonyl-[2(R)-hydroxy-2-phenylethyl]amide A solution of 1.2 g of 4'-chlorobiphenyl-4-carboxylic acid and 715 pi of triethylamine in 20 ml of dry DMF is cooled to -20° and treated with 0.710 ml of isobutylchloroformate. The reaction mixture is stirred for additionally 20 minutes and a solution of 955 mg crude (74 %) 2-amino-1(R)-phenyl-ethanol in 5 ml of DMF is added. The mixture is allowed to come to room temperature and stirred for 16 hours. The slurry is poured onto 100 ml of ice-cold water, the precipitate is collected on a sinter funnel and washed three times with water and once with ethanol. Drying to constant weight yields the compound as pale yellow crystals; m.p.: 229.3°; [ot]D20 = + 48.1° (c = 1.0, DMSO); 1H-NMR (DMSO-d6) 5 = 8.62 (t, J = 5.6 Hz; 1H); 7.95/ 7.78/ 7,55 (3d, J = 8.5 Hz; 8H); 7.41-7.22 (m; 5H); 5.55 (d, J = 4.4 Hz; 1H); 4.81 (ddd, J = 4.4, 4.7, 8.1 Hz; 1H); 3.56-3.46/3.40-3.29 (2m; 2H). c) 2-(4'-Chlorobiphenyl-4-yl)-5(S)-phenyl-4,5-dihydro-oxazole A solution of 1.24 g of 4'-chlorobiphenyl-4-carbonyl-[2(R)-hydroxy-2-phenylethyl] amide in 20 ml of pyridine is cooled in an ice bath and treated with a solution of 921 mg of methanesulfonic acid anhydride in dichloromethane. The reaction mixture is stirred for additional 16 hours at 5 °, ethyl acetate and saturated aqueous sodium hydrogencarbonate are added, the organic layer is separated, dried and concentrated in vacuo. Vacuum flash chromatography on silicagel (toluene / ethyl acetate = 3/1) yields the compound as pale yellow crystals; m.p.: 121.5° (recrystallized from ethanol); fa]D20 = + 133.5° (c = 1.3, methanol); 1H-NMR (CDCI3) S = 8.09/ 7.63/ 7.56/ 7.43 (4d, J = 8.5 Hz; 8H); 7.44-7.36 (m; 5H); 5.68 (dd. J - 7.9, 10.1 Hz, 1H); 4.51/4.02 (ABX, J = 14.9, 10.1, 7.9 Hz; 2H) . H) (+) and (->-1-Amino-1--2-ethane a) 1-[(1S)-Camphanoyl]amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yI)ethane To a solution of 0.38 g of 1-amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane (racemic compound, see A) above) in 4 mi of dry dichloromethane is added 0.26 g (0.36 ml) of triethylamine. The mixture is stirred and cooled to-79°. Then 0.44 g of (1S)(-)-camphanic acid chloride are added in such a way that the temperature does not exceed -74°. Stirring is continued for additionally 90 minutes without further cooling. For working up the mixture is poured onto ice-water, extracted three times with dichloromethane and washed with brine. After drying with sodium sulfate the solvent is evaporated. A mixture of the two diastereomeric amides is obtained which is separated by chromatography over silicagel (dichloromethane / methanol / heptane = 10/1 / 5). The two compounds are obtained as white crystals: - diastereomer B: m.p.: 195-199° - diastereomer A: m.p.: 151-160°. b) (+)- and H-1-Amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane 0.16 g of the camphanoyl diastereomer B are heated with 0.8 ml of 35% perchloric acid in a glass autoclave for 12 hours at 120°. After dilution with 2 ml of water the mixture is extracted with ethyl acetate (which is discarded). The aqueous phase is made alkaline with 2N sodium hydroxide and extracted three times with ethyl acetate. The organic layer is dried over magnesium sulfate and evaporated to dryness. Chromatography over silicagel (dichloromethane / methanol / heptane = 10/1/5 -» 7/1/ 4) yields the (+)-enantiomeric title compound (B isomer) as a pale yellow oil: 'H-NMR (CDCI3) 5 =: 8.57 (d, J=2.5Hz, 1H); 7.61 (dd, J, 2.5, J2 = 8.3Hz, 1H);7.38(s, 1H); 7.13 (d, J^ 8.3; 1H); 7.02 (s, 1H); 6.83 (s, 1H); 4.32-4.14 (m, 3H); 1.73 (s,b, 2H). Analogously as described above the (-)-enantiomeric title compound (A isomer) is obtained by hydrolysis of the camphanoyl diastereoisomer A. I) 2-Phenyl-2"(1H-imidazol-1-yl)-1-aminoethane The compound is obtained from 2-phenylazirrdine analogously as described above under E) c). Chromatography on silicagel (dichloromethane * methanol / aqueous NH3 = 10/1/0.1) gives the title compound as a cotouttess viscous oil The compounds of formula I in free form or pharmacologically acceptable salt form, hereinafter briefly referred to as "the agents of the invention", exhibit pharmacological activity and are therefore indicated for use as pharmaceuticals, in particular they are strong, selective inhibitors of the 25-hydroxyvitamin D3 - hydroxylases, which attack the C20-27 - side chain of calcitriol, e.g. the 25(OH)D3-24-hydroxylase, and thereby catabolize hormonally active vitamin D3-metabolites (e.g. calcitriol), while they interfere much more weakly with the synthesis of calcitriol itself, which occurs via the 25(OH)D3~1 -hydroxylase. Selective inhibition may e.g. be determined by the following test methods: Activity of the 1-hydroxylase: This can be determined in confluent cultures of human keratinocytes directly, while for determination of the activity of the hydroxylases attacking the C20-27 - side chain a 16 hours pretreatment schedule of the confluent cultures with 1,25(OH)2D3 (10 nM) has to precede which upregulates these activities (both methods arc described in Bikle, D.D. et al., J. Clin. Invest. 78, 557 [1986]). Keratinocyte cultures: Normal human keratinocytes are isolated from fresh adult skin obtained from mammary reduction and immediately used under stenle conditions, isolation and cultivation under serum-free conditions and without a feeder layer follows a modified protocoll as used by Bikle et al., Biochemistry 25 (1986) 1545-1548. These conditions are chosen in order to avoid undefined contributions from vitamin D - metabolites possibly retained in the serum and/or feeder layer. After separation of the epidermis from the dermis with a sterile dermatome the epidermis is incubated in a 0.25 % trypsin solution for 45 minutes at 37°. Thereafter the cells are scraped off and put in 50 ml of HBSS containing 10 % FGS to block further trypsin digestion and centrifuged at 2000 rpm for 2 minutes. The resulting ceil peilet suspended in KGM, a defined serum-free medium at low (0.06 mM) calcium concentration containing 0.1 ng/ml EGF, 5 pg/ml insulin, 0.5 pg/ml hydrocortisone, bovine pituitary extract and antibiotics (gentamycin, amphothericin) gives the primary culture. After 24 hours at 37° in an incubator with carbogen gassing (95 % Os/ 5 % C02) the unattached cells are removed, the flask washed and provided with fresh KGM. The culture medium is changed then every alternate day and the cells are passaged when they reach 80-90% confluency (usually 6 to 10 days after plating). For passaging old KGM is removed and the attached keratinocytes displaced by a short treatment (5 minutes) with 0.125 % of trypsin, then put into HBSS + FCS, centrifuged and eventually resuspended in KGM in such a way that 1 plate of primary culture yields 3 plates first passage cells. In order to expand the final cell number keratinocytes are further cultivated as described above and generally used in their second passage. a) Selective inhibition of vitamin D3 - hydroxylases: Confluent cultures of human keratinocytes in KGM at low calcium (0.06 mM) have a high capacity to produce calcitriol via the 1-hydroxylase, however, activities of sequential metabolism via side chain oxidation are almost entirely lacking. Therefore, the inhibition of the 1-hydroxylase in the confluent cultures is determined directly, and the inhibition of sequential metabolism after up-regulation of the respective hydroxyJases, e.g. the 24-hydroxylase, is determined by an overnight (17 hours) pretreatment with 10 nM of calcitriol as described by Bikle et al. (1986) (supra). The activities of the 1-hydroxylase and of particular steps in the sequential metabolism [e.g. formation of 1,24,25(OH)3D3 + 1,24oxo,25(OH)2D3] which still retain calcitriol-like activities, the formation of 3-epi caicitrio! metabolites, of polar metabolites retained in the water phase and those indicative of side-chain cleavage and their inhibition by the test compounds are determined by following the oxidation of 3H-25(OH)D? (Amersham; specific activity about 0.61 mCi/nmole) as follows: Confluent human ke-atinocytes In 1 mt of KGM and in 6-weti plates are incubated in duplicate at 37° with 3H-2S{OH)D3 for 1 hour (1 -hydroxylase), 4 hours (sequential metabolism) and for a range of time interals between 1 and 24 hours, without and after preincubation with 10 nM of calcitriol, and without and with test inhibitory compounds added in a concentration range between 0 and 10 yM Thereafter, the reaction is stopped with 1 m! of methanol per we!!, the cells are scraped off, transferred to a test tube together with the supernatant and two washings (with 1 ml of methanol and 0.8 ml of water). Unmodified 3H-25(OH)D3 and most of the products are totally extracted from the combined solutions and the cell pellet by sequential extractions with 2.1 ml and 1 ml of CHCI3 at room temperature. 3H-activity in the CHCI3-phase, in the water, and total 3H-yield is determined. Incubations for extended time intervals (> 4 hours) give rise to a high increase of 3H-activity in the wafer phase due to highly polar metabolites and a significant loss of 3H-activity in volatile products, almost entirely due to side chain cleavage in which the 3H-label at C26/27 is split off. The combined CHCI3 extracts are then evaporated under argon ai 35°, the residues dissolved in 0.4 mi of ethanoi and an aliquot subjected to HPLC-analysis on a Zorbax-Sil column (Dupont; 4.6 x 250 mm) using a non-linear gradient from 97 : 3 to 85 : 15 of hexane : 2-propanol at a flow rate of 2 ml/min and a total run time of 70 minutes. Substrate and individual metabolites are assigned to peaks by matching with unlabeled standards in co-chromatography. The extent of distinctive product formation in the presence of a particular inhibitor at concentrations ranging from 0 to 10 pM is determined and the strength of inhibition (IC50) calculated from a Dixon Plot (1/rate versus inhibitor concentration). Selectivity can be assessed by comparing the IC50 values of a distinct inhibitor for particular sequential processes and for the 1-hydroxylase. b) 3H-Thymidine incorporation into human keratinocytes - antiproliferative effects of vitamin D - metabolites in the presence of selective inhibitors of their catabolism: 3H-Thymidine incorporation is measured in 96-well plates as follows: Keratinocytes in 200 pi of 'KGM at low calcium concentration are plated at an initial density of 104 cells per well (second passage) and kept for 24 hours at 37° in an incubator with carbogen gassing (95 % O^ / 5 % COz). Thereafter, the test compounds are added in I p! of ethanoi in a range of concentrations between 0 and 10 uM in the presence and absence of 25{OH)D3 or 1a,25(OH)2D3 (both in a range between 0 and 7 nM), each concentration in triplicate. Blanks containing the solvent only or the vitamin D - metabolite are located after each well-triplet. 5 to 10 blanks per plate in the absence of solvent are added. After further 24 hours 50 pi of 3H-thymidine (1 uCi) in KGM are added, incubation continued for an additional 17 hours and eventually stopped by cell harvesting and lysis. Harvesting is done on a Filtermate 19fi - Harvester (Packard-Canberra), in a first step, the supernatants are soaked through a 96-weli filterplate and washed 3x with water. Measurement of these filterplates as described below clearly shows that no cells with incorporated 3H-activity have been shed off. Then the adherent cells in the incubated plates are released by treatment with 100 pi of 0.125 % trypsin in PBS at 37° for 5 minutes, harvested on a new filterplate and washed 3x with water. 50 pi of scintillation cocktail (MicroScint O, Packard) are added and 3H-activity is counted on a Microplate Scintillation Counter (Topcount, Packard Canberra). Data are used as means ± SEM (n = 3). The iC50-values for the inhibition of proliferation by the vitamin D - metabolites in the presence of varying concentrations of inhibitors of side chain metabolism and vice versa are assessed by plotting the inverse proliferation rate versus one inhibitor concentration, with the concentration of the other inhibitors kept constant (Dixon Plot). Independent of the mechanism of inhibition the IC50-values can be read in this plot from the intercept on the x-axis. The agents of the invention show inhibitory activity in the above tests a) and b) at concentrations of from about 0.01 pM to about 10 pM. The agents of the invention are therefore indicated for use as selective inhibitors of the 25-hydroxyvitamin D3 - hydroxylases which attack the C20-27 - side chain of vitamin D3, in the treatment of disorders of proliferation and differentiation in vitamin D - responsive tissues, particularly for the treatment of conditions where it is desired to selectively inhibit the catabolism of the hormone calcitriol without interfering with its synthesis from its precursor 25(OH)D3, such as to increase and prolong endogenous hormone levels and therefore exert beneficial effects with respect to proliferation and differentiation, to immune function and to calcium homeostasis, such as, for skin, in hyperproliferative and inflammatory diseases such as psoriasis and eozematous diseases, in degenerative changes of connective tissue both pathologic and accompanying normal aging, in the prevention of hair loss and regeneration of hair growth, and beyond skin, in tumor suppression, in increasing tolerance against ailotransplantates, in rheumatoid arthritis and in bone remodeling. For these indications the appropriate dosage will, of course, vary depending upon, for example, the agent of the invention used, the host, the mode of application and the intended indication. However, in general, satisfactory results in animals are indicated to be obtained at a daily dosage from about 1 mg/kg to about 20 mg/mg animal body weight. In larger mammals, for example humans, an indicated daily dosage is in the range from about 70 mg to about 1400 mg of an agent of the invention conveniently administered, for example, in divided doses up to two or four times daily for enteral/systemic treatment, and in the concentration range of less than 0.5 %, e.g. 0.1 %, to about 2 % in a cream/solvent for topical treatment. The agents of the invention may be admixed with conventional pharmaceutical^ acceptable diluents and carriers and, optionally, further excipients. They may be administered by any conventional route, in particular enterally, e.g. orally, e.g. in the form of tablets or capsules, or topically, e.g. in the form of lotions, gels, creams, sprays and solutions such as ophthalmic or nasal solutions or aerosols for local treatment of skin and mucosal membranes, such as the eye, respiratory tract, vagina, oral and nasal cavity. They may be administered alone or in combination with low doses of calcitriol or with standards such as cyclosporin A (SandimmunR) to enhance immune suppressive and antiinflammatory effects; far lower doses of the individual drugs than usual will reduce undesired side effects. The agents of the invention may substitute for therapy with glucocorticoids (e.g. dexamethasone, betamethasone, prednisolone) and other immune suppressive agents and may supplement treatment with calcitonin and parathyroidal hormone. The enantiomeric compounds N-[4-(4-chlorophenyl)benzoyl]-2-(1 H-imidazo!-1 -yl)-2(S)-phenyl-1 -aminoethar.e (example 8) and its (R)-enantiomer (example 9), are the preferred agents in the above indications. They are selective inhibitors of the 25-hydroxyvitamin D3 -hydroxylases which attack the C20-27 - side chain of vitamin D3 without interfering with its synthesis from the precursor 25(CH)D3. !t has, for example, been determined that they have an !C50 of between 10 nM and 50 nM in the above two tests a)-and b) for the inhibition of side chain metabolism, eg. for, respectively, the (S)- and the (R)-enantiomer: - in test a): 40 nMand12 nM, respectively, as regards stabilization of 3-epi 1,25(OH)2D3 levels and 45 nM and 19 nM as regards stabilization of levels of the sum of 1,25(OH)2D3, 1,24,25(OH)3D3 and 1,24oxo,25(OH)2D3, but an IC^ of 530 nM and 620 nM, respectively, for inhibition of 1-hydroxylase; - in test b): an IC50 of 30 nM and 35 nM, respectively, as regards the concentration required to double the antiproliferative effect of ia,25(OH}JD3t and 11 nM and 12 nM for 25(OH)D3. It is, therefore, indicated that for treatment in e.g. psoriasis they may be administered at a concentration of from about 0.1 % to about 0.5 % by topical administration to large mammals, for example humans, by similar modes of administration as conventionally employed. The invention also provides pharmaceutical compositions for e.g. topical application comprising an agent of the invention together with at least one pharmaceutically acceptable carrier or diluent. Such compositions may be manufactured in conventional manner by mixing an agent of the invention together with at least one pharmaceutically acceptable carrier or diluent. Unit dosage forms contain, for example, from about 20 mg to about 700 mg of active substance. The use in the treatment of psoriasis is preferred. The agents of the invention exhibit more pronounced and selective 25(OH)D3 - hydroxylase inhibiting activity than would be expected for structurally similar compounds. Claims: 1. A compound of formula I wherein either R, represents phenyl, naphthy!, thieny! or pyridyl, whereby these four substituents are optionally monosubstituted by halogen, alkoxy, alkyl, dialkylamino or cyano and R2 represents hydrogen; or R1 represents hydrogen and R2 represents pyridyl or 2(5 ch!orc)pyridy!; R3 represents hydrogen, halogen, alkylr cyanc, alkoxycarbony!, alkylcarbonyl or optionally substituted amino; and X represents CH or N; in free form or salt form. 2 A compound according to claim 1 of formula wherein eitherR1P represents phenyl optionally monosubstituted by chlorine in 4 position and R2p represents hydrogen or R,p represents hydrogen and R2p represents 2-(5-chloro)pyridyl, and Xp represents CH or N; or R,p represents 1-naphthyl, R2p represents hydrogen and Xp represents CH; in free form or pharmacologically acceptable acid addition salt form. 3. The compound N-[4-(4-chlorophenyl)benzoyl]-2-(1H-imidazol-1-yl)-2-phenyl-1-aminoethane in racemic or in 2(S)- or 2(R)-enantiomeric form; in free form or salt form. 4. A compound according to claim 1 wherein X represents CH and either R, represents hydrogen and R2 and R3 respectively represent - 2-(5-chloro)pyridyt and 4-chloro, in racemic or (+)- or (-)-enantiomeric form, or represent - 2-pyridy! and 4-ch!cro, or - 3-pyridyl and 4-chloro, or - 4-pyridyl and 4-chloro, or - 2-(5~chloro)pyridy! and 4-ethoxy: or - 2-(5-ch!oro)pyridy! and 4-n-butoxy; or R2 represents hydrogen, R3 represents 4^hioro and Rj represents - 4-chlorophenyl, in racemic or (+)(S)-enantiomeric form, or represents - 1-naphthyl; in free form or salt form. 5. A process for preparing a compound according to claim 1 comprising a) acylating a corresponding compound of formula wherein the substituents are as defined in claim 1, to introduce a corresponding biphenyl-4-carbonyl group; or b) for the preparation of a compound of formula la wherein R3 and X are as defined in claim 1 and R/ has the same significance as R, as defined in claim 1 but without hydrogen, reacting a corresponding compound of formula wherein R/ is as defined in this claim and R3 is as defined in claim 1, with the corresponding compound of formula wherein X is as defined in claim 1; and recovering the resultant compound of formula I in free form or salt form. 6. A pharmaceutical composition comprising a compound of any one of claims 1 to 4 in free form or pharmacologically acceptable salt form together with at least one pharmaceutical^ acceptable carrier or diluent.

Documents:

496.jpg

mas-1995-496-abstract.pdf

mas-1995-496-claims duplicate.pdf

mas-1995-496-claims original.pdf

mas-1995-496-correspondace others.pdf

mas-1995-496-correspondace po.pdf

mas-1995-496-description complete duplicate.pdf

mas-1995-496-description complete original.pdf

mas-1995-496-form 1.pdf

mas-1995-496-form 26.pdf

mas-1995-496-form 3.pdf

mas-1995-496-form 4.pdf