Patent Application
20090275607
The present invention relates to medicine chemistry field, particularly relates to a kind of tetrahydro isoquinoline derivatives and the preparation methods, pharmaceutical compositions and medicinal uses thereof, more particularly relates to the use as κ-opioid receptor agonist in analgesic.
κ-Receptor, together with μ-, δ-, α-, and ORL-1 receptors, belongs to opioid receptor family. μ-Receptor agonist medicine, represented by morphine, has powerful analgesic efficacy, but has many limits in clinical uses due to its side effects, such as dependence and addiction. The central selective κ-receptor agonist not only can be used for analgesic, but also can avoid morphine-like side effects. It can be used for analgesic, antiphlogistic and analgesic, anti-hyperpathia, treating labor pain; used as aquaretic agents, antipruritic; and used for anticonvulsant treatment, anti-hypertension, neural protection, treating HIV infection, and also used in withdrawal of cocaine and morphine addiction. Therefore, selective κ-receptor agonist medicine has good application prospect.
The present invention discloses a series of novel tetrahydro isoquinoline derivatives. According to radioligand binding assays, the compound of the invention has very high compatibility and selectivity for κ-receptor. In analgesic test for mice, it shows good analgesic activity.
The general formula I of the compound of the invention is as below:
wherein R1 represents:
R2 each independently represents: H, F, Cl, Br, C1-C4 alkyl, OR5, or NR6R7, or form 5,6-methylenedioxy, 6,7-methylenedioxy, or 7,8-methylenedioxy together.
R3 and R4 each independently represent: H, F, Cl, Br, trifluoromethyl, C1-C4 alkyl, OR5, NR8R9, or form 4,5-methylenedioxy, 5,6-methylenedioxy, or 6,7-methylenedioxy together.
R5 represents: H, C1-C4 alkyl, allyl, C3-C7 cycloalkyl (preferably cyclopropyl, cyclobutyl, or cyclopentyl);
R6 and R7 each independently represent: H, C1-C4 alkyl, C1-C4 alkylacyl (preferably formyl, acetyl, or propionyl), or C1-C4 alkylsulfonyl (preferably methylsulfonyl, or ethylsulfonyl);
R8 and R9 each independently represent: H, C1-C4 alkyl, allyl, C1-C4 alkylacyl (preferably formyl, acetyl, or propionyl), or C1-C4 alkylsulfonyl (preferably methylsulfonyl, or ethylsulfonyl); or form 3-7 membered ring group together with N atom.
Preferably, the compound of general formula I is:
R1 represents
R2 each independently represents: H, F, Cl, methyl, hydrox, methoxy, dimethylamino, or form 5,6-methylenedioxy or 6,7-methylenedioxy group together;
R3 and R4 each independently represent: H, F, Cl, methyl, hydroxyl, methoxy, dimethylamino, or form 4,5-methylenedioxy, 5,6-methylenedioxy or 6,7-methylenedioxy together.
More preferably, the compound is:
R1 represents
R2 each independently represents H, F, Cl or methoxy; R3 and R4 represent H, F, Cl, or methoxy.
Most preferably, the compound is
R1 represents:
R2 represents H, R3 represents H, and R4 represents Cl.
According to the present invention, the pharmaceutically acceptable salt comprises acid addition salt formed by the compound of the general formula I and the following acids: hydrochloric acid, hydrobromic acid, sulfuric acid, carbonic acid, citric acid, tartaric acid, phosphoric acid, lactic acid, pyruvic acid, acetic acid, maleic acid, mesylate, benzene sulfonic acid, β-toluene sulphonic acid, or arginine.
Part compounds of the present invention are:
The preparation method for the compound of general formula (I) of present invention is as below:
acetonitrile, N,N-dimethylformamide, N,N-dimethylacetamide, or dimethyl sulfoxide) to obtain the compound of general formula (I).
1-(pyrrolidine-1-methyl)-1,2,3,4-tetrahydroisoquinoline series intermediate (VI) is synthesized from (substituted)β-phenylethylamine (general formula II), and the preparation method is as below:
2,3-dihydro-inden-3-keto-1-carboxylic acid series intermediate (XI) is synthesized from (substituted) benzaldehyde (general formula VII), and the preparation method is as below:
Note: when the raw material is benzaldehyde, route A is adopted; when the raw material is substituted benzaldehyde, route B is adopted.
According to the results of radioligand binding assays, the compound of general formula (I) and its pharmaceutically acceptable salt have very high affinity for κ-receptor while having low or extremely low affinity for Preceptor, and exhibit good selectivity for κ-receptor. In the analgesic ability test which model are mice hot plate method and mice writhing method, it shows good analgesic effect.
The present invention further relates to a pharmaceutical composition for treating diseases relevant to κ-opioid receptor agonist, which contains effective dose of the compound of general formula (I) and pharmaceutically acceptable carrier. The pharmaceutical composition can be in routine preparation forms, such as common tablet or capsule, sustained release tablet or capsule, controlled release tablet or capsule, or injection, etc.
The present invention further relates to the application of the compound of general formula (I) in preparation of medicine for treating or preventing diseases relevant to κ-opioid receptor agonist; wherein the medicine for treating or preventing diseases relevant to κ-opioid receptor agonist is selected from medicines for analgesic, antiphlogistic and analgesic, anti-hyperpathia, and treating labor pain; or medicines for anticonvulsant treatment, anti-hypertension, neural protection, or treating HIV infection; or medicines for withdrawal of cocaine and morphine addiction; or aquaretic agents, antipruritic. Preferably, the disease related to κ-opioid receptor agonist is surgical or cancer pain.
The preparation embodiments for partial active compounds are as below:
RY-1 type melting point tube; Nicolet Impact 410 IR spectrometer, KBr pellet; 1H-NMR by Bruker AM-500 NMR spectrometer, internal standard TMS; HP1100 Mass spectrograph; Agilent 1100 series LC/MSD Trap SL; Carlo Erba 1106 element analyzer.
Add β-phenylethylamine 36.3 g (0.3 mol), sodium carbonate 31.8 g (0.3 mol), and dichloromethane 300 ml into 500 ml three-necked bottle, control temperature at 0° C. through ice bath, slowly dropwise add chloroacetyl chloride 40.68 g (0.36 mol) within 1 h while stirring, further react at 0° C. for 2 h while stirring to give white turbid solution, slowly add ice water 150 ml, and separate organic layer. Wash the organic layer sequentially with 10% dilute hydrochloric acid solution and saturated salt water, dry with anhydrous sodium sulfate, vacuum evaporate to remove solvent, recrystallize the residue with methanol-water, filter, dry, obtain white needle crystal III-1 36 g, with yield of 61% and mp 61-63° C. (reference value: 60-63° C.).
Add xylene 300 ml and phosphorus pentoxide 28.4 g (0.2 mol) into 500 ml three-necked bottle, increase temperature to 140° C. while mechanical stirring, add compound III-1 9.48 g (0.048 mol) in batch under nitrogen gas protection and immediately the solution turn yellow, react for 3 h under reflux. Cool, and pour out xylene. Slowly add ice water 450 ml into solid residue under ice bath cooling, stir solution for 0.5 h, regulate pH to 11 with 50% NaOH, extract with ethyl ether, and dry with anhydrous sodium sulfate overnight. Filter, introduce dry HCl gas into the filtrate under ice bath, the solution turns from turbid to clear, yellow solid is precipitated on the bottle wall, pour out the solvent and dry it to obtain IV-1 5.3 g, with yield of 51% and mp of 161-163° C. (reference value 163-164° C.).
Add methanol 40 ml and tetrahydropyrrole 3.55 g (0.05 mol) under nitrogen gas protection into 100 ml three-necked bottle, control temperature at 0° C. through ice bath, slowly dropwise add methanol solution of compound IV-1 2.66 g (0.0123 mol) while stirring. The temperature of reacting solution is increased to room temperature after dropwise addition, and react overnight to give red transparent solution V-1 which can be directly used for next step of reaction.
controlling temperature at 0° C. through ice bath, add NaBH4 1.68 g (0.025 mol) in batch into the V-1 solution of the above step, release hydrogen gas and the solution turns to yellow turbid solution. The reacting solution temperature is increased to room temperature after 3 h, evaporate to remove solvent, treat the residue with NaOH and extract it with ethyl ether. Dry the ether layer with anhydrous sodium sulfate overnight. Filter, and evaporate solvent to give orange oil VI-1 crude product 1.46 g, with yield of 55%, which is directly used for next step of reaction.
Add benzaldehyde 21.2 g (0.2 mol), diethyl malonate 32 g (0.2 mol), piperidine 1.2 ml, benzoic acid 0.6 g, and benzene 60 ml into 250 ml eggplant-shaped flask, increase temperature until intensive reflux occurs, use water separator to separate water, and react for 18 h; vacuum evaporate to remove benzene, extract with chloroform-water, wash the organic layer sequentially with water, 1 mol/l hydrochloric acid, and saturated sodium hydrogen carbonate solution, and dry with anhydrous sodium sulfate overnight. Filter, and vacuum evaporate to remove solvent to give orange oil component VIII-a 42.5 g, with yield of 80%, which is directly used for next step of reaction (the pure ester can be obtained by distillation, b.p. 140-142°/4 mm).
Add 20 ml aqueous solution of compound VIII-a 50 g (0.2025 mol) and KCN 14 g (0.215 mol), and 500 ml ethanol into 1 L three-necked flask, increase temperature to 65-75° C., react for 18 h while stirring. Cool to 15° C. after reaction, filter to remove KHCO3, wash the filter cake with 20 ml ethanol and combine it with the filtrate. Carefully acidify with diluted hydrochloric acid 5 ml, vacuum concentrate to semi-solid state. Cool, extract with ethyl ether-water, dry the organic layer with anhydrous calcium chloride, filter, and vacuum evaporate to remove solvent to give red oil component IX-a 27 g, with yield of 66%, which is directly used for next step od reaction. (the pure ester can be obtained by distillation, b.p. 161-164°/8 mm).
Add compound IX-a 35 g (0.172 mol) and concentrated hydrochloric acid 125 ml into 250 ml eggplant-shaped flask, heat to reflux for 18 h to precipitate orange solid, recrystallize with water, decolore with activated carbon to give pale orange liquid, and freeze to precipitate white solid X-1 27.5 g, with yield of 70%, and m.p. 163-164° (reference value: 163-164°).
Add compound X-1 crude product 3 g (0.017 mol) and SOCl2 3 ml into 25 ml three-necked flask, mechanically stir, increase temperature to reflux for 0.5 h, slightly cool, add anhydrous nitrobenzene 6 ml and anhydrous AlCl3 3 g (0.0225 mmol), react at 80° C. for 1.5 h, pour to ice water 75 ml, steam distill to remove all nitrobenzene, add activated carbon 1.5 g for decoloring, hot filter, rapidly shake for cooling to give white water-containing acid with m.p. 84° C. After drying, finally obtain anhydrous acid XI-1 1.2 g, with yield of 61% and m.p. 119-120° C. (reference value 120° C.).
Add compound VI-1 0.97 g (4.5 mmol), compound XI-1 0.95 g (5.4 mmol), DMAP at catalyst quantity, and CH2Cl2 20 ml into 50 ml three-necked flask, control temperature at 0° C. through ice bath and stir for 0.5 h, slowly dropwise add DCC 1.3 g (6.3 mmol) dissolved in 10 ml of CH2Cl2 solution, react overnight under protection of nitrogen gas. React solution turns to orange turbid solution, filter to remove DCU. Subject to column chromatography with petroleum ether:ethyl acetate:triethylamine=4:1:0.1 to give white solid I-1 0.67 g, with yield 40% and mp. 120-122° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.74˜7.78 (2H, m, ArH19,19), 7.60 (1H, m, ArH20), 7.15˜7.43 (12H, m, ArH20,21,21,22,7,7,8,8,5,5,6,6), 6.99˜7.01 (1H, d, H22), 5.81/5.46˜5.49 (2H, dd/dd, H1,1), 4.99˜5.01/4.68 (2H, dd/dd, H16,16), 4.77˜4.80/4.27˜4.31 (2H, m/m, H3,3), 3.92˜3.98 (1H, m, H9), 3.32˜3.37 (1H, m, H3′), 2.45˜3.17 (20H, m, H3′,9,9′,9′H17,17,17′,17′, H4,4,4′,4′, H11,11,11′,11′, H14,14,14′,14′), 1.67˜1.81 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
(Note: 1. As the molecule contains two chiral carbons, the product contains two pairs of diastereoisomers, i.e. RR/SS and RS/SR; therefore 1H-NMR spectrum shows two groups of hydrogen, this phenomena is also reported in literatures (Charles B K, Willem A L, Joseph P M. Tetrahedron, 2003, 59:8337-8345), and the underscore “_” represents isomers with relatively high content, the same below))
IR (cm−1): 3415, 2962, 2929, 2790, 1712 (C═O), 1641 (C═O), 1604, 1434, 1284, 1238, 1043, 761
MS (ESI(+) 70V, m/z): 375.2 ([M+H]+, base peak)
Anal. Calcd. for C24H26N2O2: C, 76.98; H, 7.00; N, 7.48. Found: C, 76.88; H, 7.07; N, 7.43.
Add 3,4-dimethoxy benzaldehyde 26 g (0.16 mol), ethyl cyanoacetate 18 g (0.16 mol), piperidine 0.8 ml, acetic acid 2.4 g, and benzene 60 ml into 250 ml eggplant-shaped flask, increase temperature to 120-130° C. for intensive reflux, separate water with water separator, react for 12 h. Vacuum evaporate to remove benzene, pour ice water into the reaction solution to precipitate yellow solid, filter and dry to obtain pale yellow crystal VIII-b-2 41 g, with yield almost reaching theoretical value and m.p. 154-156° C. (reference value 156° C.).
Add the compound VIII-b-2 52.2 g (0.2 mol), 15 ml of aqueous solution of KCN 14.3 g (0.22 mol), and ethanol 180 ml, reflux react for 40 min while stirring. Cool, carefully add diluted hydrochloric acid for acidification, stir at room temperature overnight. Filter and dry to give white solid. Place the filtrate in refrigerator to precipitate solid again, extract with chloroform-water, and vacuum evaporate to remove chloroform, totally obtain white solid IX-b-2 35 g, with yield of 60% and mp 92-94° C. (reference value 93-95° C.).
The compound IX-b-2 is subjected to the same procedure as preparation of X-1, and refluxed for 8 h under heat; the crude product is recrystallized with water, and decolored with activated carbon to give white solid X-2, with yield of 75% and m.p. 173-174° C. (reference value 172-174° C.).
Add PPA 30 g (15 times of the reactant weight) into 25 ml three-necked flask, increase temperature to 70° C. while mechanical stirring, add compound X-2 2 g (8.47 mmol), the color of the reaction system turns from gray to yellow, then to dark red, react at 70° C. for 4 h under nitrogen protection, pour into ice water, extract with chloroform, evaporate to obtain pale yellow solid. Recrystallize with water to give white solid XI-2 1.3 g, with yield of 70% and m.p. 190-190.5° C. (reference value 190-191° C.).
The compound VI-1 and X-2 are subjected to the same procedure as preparation of 1-1 to give white solid I-5, with yield of 35% and mp 124-125° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 6.95˜7.27 (10H, m, ArH19,19,7,7,8,8,6,6,5,5), 6.30/6.95 (2H, s/s,22,22), 5.80˜5.82/5.51˜5.53 (2H, dd/dd, H1,1), 4.85˜4.88/4.55˜4.57 (2H, dd, H16,16), 4.82˜4.83/4.21˜4.25 (2H, m, H3,3), 3.09, 3.84, 3.91, 3.95 (12H, s, OCH3, OCH3), 3.38˜3.48 (1H, m, H3′), 3.13˜3.17 (1H, m, H9), 2.45˜3.07 (20H, m, H3′, H9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11,11′,11′, H14,14,14′,14′), 1.62˜1.81 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3493, 2961, 2924, 2805, 2794, 1673 (C═O), 1635 (C═O), 1594, 1503, 1442, 1311 (C—O—C), 1266, 1218, 1191, 1119, 1044 (C—O—C), 854, 771
MS (ESI(+) 70V, m/z): 435.2 ([M+H]+, base peak)
Anal. Calcd. for C26H30N2O4H2O: C, 69.01; H, 7.13; N, 6.19. Found: C, 68.94; H, 7.08; N, 6.14.
Use 3-chlorobenzaldehyde as raw material, and perform the same procedures as preparation of VIII-b-2 to give yellow crystal VIII-b-3, with yield almost of theoretic value and mp 100-101° C. (reference value 101° C.).
Add the compound VIII-b-3 53 g (0.225 mol), 16 ml of aqueous solution of KCN 15.5 g (0.237 mol), and ethanol 330 ml, react at room temperature for 18 h while stirring. Carefully add diluted hydrochloric acid for acidification, filter to remove solid insoluble matter, vacuum concentrate, extract with chloroform-water, and vacuum evaporate to remove chloroform to give brown oil matter IX-b-3 36 g, with yield of 62%.
The compound IX-b-3 is subjected to the same procedure as preparation of X-1, and refluxed for 8 h under heat; the crude product is recrystallized with ethyl ether-petroleum ether, and decolored with activated carbon to give white solid X-3, with yield of 70% and m.p. 158-160° C. (reference value 161-162° C.).
The compound X-3 is subjected to same procedure as preparation of XI-1 to give carneous solid mixture of XI-3 and XI-4. After column chromatography separation, white solid XI-3 is obtained, with yield of 50% and mp 146-148° C. (reference value: 148-151° C.); white solid XI-4 is also obtained, with yield of 10% and mp 171-174° C. (reference value 171-174° C.).
The compound VI-1 and XI-3 are subjected to the same procedure as preparation of I-1 to give white solid I-6, with yield of 38% and mp 120° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.66˜7.70 (2H, m, ArH20,20), 7.60/6.97 (2H, s/s, ArH22,22), 7.40˜7.42/7.31˜7.33 (2H, dd/dd, ArH19,19), 7.14˜7.29 (8H, d, ArH7,7,8,8,5,5,6,6), 5.80˜5.83/5.37˜5.39 (2H, dd/dd, H1,1), 4.91˜4.93/4.63˜4.66 (2H, dd/dd, H16,16), 4.74˜4.78/4.25˜4.28 (2H, m/m, H3,3), 3.94˜4.00 (1H, m, H9), 3.29˜3.33/3.22˜3.26 (2H, m/m, H3′,3′), 2.44˜3.20 (15H, m, H9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.42˜2.45/2.59˜2.62 (4H, m, H11,11′, H14,14′), 1.54˜1.79 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
13C-NMR (500 MHz, CDCl3), δ (ppm): 77.2/58.1 (C-1), 55.4 (C-3), 28.6 (C-4), 132.9/126.9 (C-4a), 124.9˜129.4 (C-5, C-6, C-7, C-8, C-19, C-20, C-22), 154.9 (C-8a), 61.6/54.8 (C-9), 41.6/40.6 (C-11), 24.0 (C-12), 23.7 (C-13), 40.9 (C-14), 179.9/171.4 (C-15), 40.5/40.4 (C-16), 36.0/29.6 (C-17), 203.9 (C-18), 134.8/134.2 (C-18a), 141.3 (C-21), 135.4/135.2 (C-22a)
IR (cm−1): 3471, 3413, 2964, 2929, 2790, 1716 (C═O), 1639 (C═O), 1596, 1440, 825, 744
MS (ESI(+) 70V, m/z): 409.2 ([M+H]+, base peak)
Anal. Calcd. for C24H25ClN2O2: C, 70.49; H, 6.16; N, 6.85. Found: C, 70.63; H, 6.31; N, 6.74.
The compound I-6 3 g (7.35 mmol) is dissolved in acetone, and dry HCl gas is introduced in ice bath to precipitate white solid I-6.HCl 2.9 g, with yield of 90% and mp 281-282° C.
Anal. Calcd. for C24H25ClN2O2.HCl.0.5H2O: C, 63.44; H, 5.99; N, 6.16. Found: C, 63.56; H, 6.24; N, 6.09.
The compound VI-1 and the compound XI-4 are subjected to the same procedures as preparation of I-1 to give white solid 1-12, with yield of 40% and mp 135-136° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.14˜7.70 (14H, m, ArH), 5.71/5.13˜5.15 (2H, dd/dd, H1,1), 4.80˜4.83/4.53 (2H, dd/dd, H16,16), 4.75˜4.79/4.02 (2H, m/m, H3,3), 2.44˜3.17 (22H, m, H3′,3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11,11′,11′, H14,14,14′,14′), 1.54˜1.87 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3446, 3425, 2956, 2925, 2854, 1724 (C═O), 1618 (C═O), 1460, 1272, 1122, 1068, 821, 779, 754
MS (ESI(+) 70V, m/z): 409.2 ([M+H]+, base peak)
Anal. Calcd. for C24H25ClN2O2: C, 70.49; H, 6.16; N, 6.85. Found: C, 70.42; H, 6.93; N, 6.56.
Use 3-methoxybenzaldehyde as raw material to carry out the same procedure as preparation of VIII-b-2 to give orange oil matter VIII-b-4, with yield of almost theoretical value, which can be directly used in next step of reaction.
Add the compound VIII-b-4 69.3 g (0.3 mol), 25 ml of aqueous solution of KCN 25.35 g (0.39 mol), and ethanol 480 ml into 500 ml three-necked flask, react at room temperature for 18 h while stirring, carefully add diluted hydrochloric acid for acidification, refrigerate, filter, dry to obtain brown-yellow solid, recrystallize with ethanol-water to obtain white solid IX-b-4 46.44 g, with yield of 60% and mp 73° C.
The compound IX-b-4 is subjected to the same procedure as preparation of X-1, and refluxed for 8 h under heat; the crude product is recrystallized with acetone, and decolored with activated carbon to give white solid X-4, with yield of 78% and m.p. 174-175° C. (reference value 174-175° C.).
The compound X-4 is subjected to same procedure as preparation of XI-2 to give white solid XI-5 with yield of 75% and mp 186-187.5° C. (reference value: 186-187.5° C.).
The compound VI-1 and XI-5 are subjected to the same procedure as preparation of I-1 to give white solid I-13, with yield of 37% and mp 143-144° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.66˜7.67/7.62˜7.63 (2H, d/d, ArH19,19), 7.12˜7.25 (8H, m, ArH20,20,7,7,8,8,5,5), 7.02/6.35 (2H, s/s, ArH22,22), 6.94˜6.95/6.81˜6.83 (2H, dd/dd, ArH6,6), 5.78/5.46˜5.49 (2H, dd/dd, H1,1), 4.89˜4.91/4.57 (2H, dd/dd, H16,16), 4.80˜4.84/4.20˜4.22 (2H, m, H3,3), 3.20, 3.87 (6H, s, OCH3, OCH3), 3.36˜3.40/3.17 (2H, m/m, H3′,3′), 2.66˜3.04 (16H, m, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.45˜2.59 (4H, m, H11,11′, H14,14′), 1.60˜1.94 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3463, 3419, 2931, 2819, 1701 (C═O), 1643 (C═O), 1596, 1433, 1286, 1244 (C—O—C), 1087 (C—O—C), 831, 748
MS (ESI(+) 70V, m/z): 405.1 ([M+H]+, base peak)
Anal. Calcd. for C25H28N2O3: C, 74.23; H, 6.98; N, 6.93. Found: C, 73.73; H, 7.41; N, 7.35.
Use 4-methoxyphenylethylamine as raw material, and carry out same procedure as preparation of III-1 to give white crystal III-2, with yield of 72% and mp 99-100° C. (reference value 99-100° C.).
The compound III-2 is subjected to the same procedure as preparation of IV-1 to give yellow solid IV-2, with yield 64% and mp 138-141° C. (reference value 138-141° C.).
The compound IV-2 is subjected to the same procedure as preparation of V-1 to give brown yellow transparent liquid V-2 which is used directly for next step of reaction.
The compound V-2 is subjected to the same procedure as preparation of VI-1 to give orange oil VI-2 crude product, with yield 60%, which is used directly for next step reaction.
The compound VI-2 and XI-1 are subjected to the same procedures as preparation of I-1 to give white solid I-14, with yield 42% and mp 135-136° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.59˜7.77 (4H, m, ArH19,19,20,20), 7.33˜7.44, 7.12˜7.14 (4H, m, ArH21,21,22,22), 7.05˜7.06/7.00˜7.02 (2H, d/d, ArH5,5), 6.83˜6.85, 6.73˜6.78 (4H, m, ArH6,6,8,8), 5.79/5.42˜5.44 (2H, dd/dd, H1,1), 4.97˜5.00/4.74˜4.76 (2H, dd/dd, H16,16), 4.77˜4.78/4.26˜4.30 (2H, m/m, H3,3), 3.88˜3.94/3.121˜3.129 (2H, m, H9,9), 3.78, 3.83 (6H, s, OCH3, OCH3), 3.32˜3.36 (1H, m, H3′), 2.52˜3.01 (19H, m, H3′, H9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11,11′,11′, H14,14,14′,14′), 1.69˜1.81 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3456, 3417, 2929, 2806, 1714 (C═O), 1639 (C═O), 1610, 1502, 1442, 1249 (C—O—C), 1153, 1037 (C—O—C), 765, 811, 765
MS (ESI(+) 70V, m/z): 405.2 ([M+H]+, base peak)
Anal. Calcd. for C25H28N2O3: C, 74.23; H, 6.98; N, 6.93. Found: C, 74.13; H, 6.88; N, 6.89.
The compound VI-2 and compound XI-2 are subjected to the same procedure as preparation of I-1 to give white solid I-15, with yield 39% and mp 122-124° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.20/7.15 (2H, s/s, ArH19,19), 7.11˜7.13/7.03˜7.05 (2H, dd/dd, ArH5,5), 6.94/6.33 (2H, s/s, ArH22,22), 6.80˜6.82 (2H, m, ArH6,8), 6.763˜6.768 (2H, m, ArH6,8), 5.76˜5.79/5.46˜5.48 (2H, dd/dd, H1,1), 4.84˜4.86/4.54˜4.57 (2H, dd, H16,16), 4.80˜4.83/4.21˜4.24 (2H, m/m, H3,3), 3.17, 3.78, 3.80, 3.85, 3.93, 3.95 (18H, s, OCH3, OCH3), 3.38˜3.42 (1H, m, H3′), 2.65˜3.14 (17H, m, H3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.44˜2.62 (4H, m, H11,11′, H14,14′), 1.63˜1.80 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3460, 2960, 2794, 1701 (C═O), 1639 (C═O), 1500, 1440, 1296 (C—O—C), 1253, 1215, 1039 (C—O—C), 856, 819
MS (ESI(+) 70V, m/z): 465.5 ([M+H]+, base peak)
Anal. Calcd. for C27H32N2O5.½H2O): C, 68.48; H, 7.02; N, 5.92. Found: C, 68.95; H, 7.15, N, 5.46.
The compound VI-2 and XI-3 are subjected to the same procedure as preparation of I-1 to give white solid I-18, with yield 40% and mp 151-153° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.65˜7.69 (2H, d/d, ArH20,20), 7.58/6.99 (2H, s/s, ArH22,22), 7.39˜7.40/7.30˜7.32 (2H, dd/dd, ArH19,19), 7.12˜7.14/7.03˜7.04 (2H, d/dd, ArH5,5), 6.83˜6.86, 6.74˜6.77 (4H, m, ArH6,6,8,8), 5.76/5.31˜5.32 (2H, dd/dd, H1,1), 4.89/4.62 (2H, dd/dd, H16,16), 4.69˜4.73/4.21˜4.24 (2H, m/m, H3,3), 3.90˜3.96 (1H, m, H9), 3.78, 3.82 (6H, s, OCH3, OCH3), 3.28˜3.32 (1H, m, H3′), 2.65˜3.03 (16H, m, H3′, H9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.46˜2.59 (4H, m, H11,11′, H14,14′), 1.64˜1.77 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3469, 3411, 2956, 2794, 1708 (C═O), 1641 (C═O), 1600, 1436, 1311 (C—O—C), 1242, 1161, 1035 (C—O—C), 881, 835, 806
MS (ESI(+) 70V, m/z): 439.2 ([M+H]+, base peak)
Anal. Calcd. for C25H27ClN2O3: C, 68.41; H, 6.20; N, 6.38. Found: C, 68.08; H, 6.32; N, 6.11.
The compound VI-2 and the compound XI-5 are subjected to the same procedure as preparation of I-1 to give white solid I-19, with yield 34% and mp 144-145° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.71˜7.72/7.63˜7.64 (2H, d/d, ArH19,19), 7.12, 7.13 (1H, d/d, ArH5), 7.03˜7.05 (2H, m, ArH5,22), 6.94˜6.96 (1H, dd/dd, ArH20), 6.76˜6.84/6.82˜6.84 (5H, m, ArH20,6,6,8,8,), 6.36˜6.37 (1H, s, ArH22), 5.75˜5.78/5.43˜5.45 (2H, dd/dd, H1,1), 4.88˜4.90/4.58˜4.60 (2H, dd/dd, H16,16) 4.80˜4.83/4.21˜4.25 (2H, m/m, H3,3), 3.24, 3.78, 3.81, 3.87, (12H, s, OCH3, OCH3),
3.37˜3.42 (1H, m, H3′), 2.64˜3.17 (17H, m, H3′, H9,9,9′,9′H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.45˜2.59 (4H, m, H11,11′, H14,14′), 1.60˜1.80 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3475, 3415, 2960, 2921, 2804, 1704 (C═O), 1645 (C═O), 1598, 1498, 1436, 1284, 1249 (C—O—C), 1037 (C—O—C), 827, 775
MS (ESI(+) 70V, m/z): 435.2 ([M+H]+, base peak)
Anal. Calcd. for C26H30N2O4.½H2O): C, 70.41; H, 7.04; N, 6.32. Found: C, 70.71; H, 7.04; N, 6.62.
3,4-dimethoxyphenylethylamine is adopted as raw material and subjected to the same procedure as preparation of III-1 to give white crystal III-3, with yield 62% and mp 94-95° C. (reference value 94-95° C.).
The compound III-3 is subjected to the same procedure as preparation of IV-1 to give yellow solid IV-3, with yield 57% and mp 194-196° C. (reference value 196° C.).
The compound IV-3 is subjected to the same procedure as preparation of V-1 to give brown yellow transparent liquid V-3 which is used directly for next step reaction.
The compound V-3 is subjected to the same procedure as preparation of VI-1 to give orange oil VI-3 crude product, with yield 55%, which is used directly for next step reaction.
The compound VI-3 and XI-1 are subjected to the same procedures as preparation of I-1 to give white solid I-26, with yield 42% and mp 174-175° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.74˜7.78 (2H, m, ArH19,20), 7.58/7.61 (2H, m, ArH19,20), 7.34˜7.45 (3H, m, ArH21,21,22), 7.00, 7.01 (1H, d/d, H22), 6.74, 6.70 (2H, s/s, ArH8,8), 6.68˜6.70, 6.61 (2H, s/s, ArH5,5), 5.71/5.37˜5.40 (2H, dd/dd, H1,1), 4.96˜4.99/4.66 (2H, dd/dd, H16,16), 4.78˜4.82/4.27˜4.31 (2H, m/m, H3,3), 3.85, 3.90 (12H, s, OCH3, OCH3), 3.34˜3.38 (1H, m, H3′), 2.66˜3.14 (17H, m, H3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.47˜2.56 (4H, m, H11,11′, H14,14′), 1.65˜1.78 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3448, 3406, 2958, 2790, 1708 (C═O), 1639 (C═O), 1515, 1436, 1257, 1234 (C—O—C), 1120, 1024 (C—O—C), 883, 837, 775
MS (ESI(+) 70V, m/z): 435.5 ([14+H]+, base peak)
Anal. Calcd for C26H30N2O4: C, 71.87; H, 6.96; N, 6.45. Found: C, 72.19; H, 6.87; N, 6.38.
The compound VI-3 and the compound XI-2 are subjected to the same procedure as preparation of I-1 to give white solid I-27, with yield 33% and mp 125° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.19/7.15 (2H, s/s, ArH19,19), 6.94/6.75 (2H, s/s, ArH22,22), 6.73/6.67 (2H, s/s, ArH8,8), 6.59/6.36 (2H, s/s, ArH5,5), 5.70˜5.73/5.40˜5.43 (2H, dd/dd, H1,1), 4.84˜4.85,4.54˜4.56 (2H, dd, H16,16), 4.81˜4.83, 4.20˜4.25 (2H, m/m, H3,3), 3.20, 3.85˜3.95 (24H, s, OCH3, OCH3), 3.37˜3.42 (1H, m, H3′), 2.65˜3.13 (17H, m, H3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.47˜2.59 (4H, m, H11,11′, H14,14′), 1.58˜1.80 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3415, 2947, 2800, 1695 (C═O), 1633 (C═O), 1500, 1442, 1307
(C—O—C), 1269, 1251, 1215, 1116, 1043 (C—O—C), 864, 775
MS (ESI(+) 70V, m/z): 495.5 ([M+H]+, base peak)
Anal. Calcd. for C28H34N2O6.H2O: C, 65.61; H, 7.08; N, 5.47. Found: C, 65.79; H, 6.86; N, 5.23.
The compound VI-3 and the compound XI-3 are subjected to the same procedure as preparation of I-1 to give white solid I-30, with yield 35% and mp 178-179° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.66˜7.70 (2H, d/d, ArH20,20), 7.59/7.00 (2H, s/s, ArH22,22), 7.40˜7.42/7.32˜7.33 (2H, dd/dd, ArH19,19), 6.69, 6.61 (4H, s/s, ArH5,8,8,5), 5.72/5.28˜5.31 (2H, dd/dd, H1,1), 4.90˜4.92/4.64 (2H, dd/dd, H16,16), 4.73˜4.77/4.24˜4.28 (2H, m/m, H3,3), 3.86, 3.90 (12H, s, OCH3, OCH3), 3.30˜3.34 (1H, m, H3′), 2.65˜3.03 (17H, m, H3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.46˜2.59 (4H, m, H11,11′, H14,14′), 1.64˜1.79 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3456, 3413, 3328, 2927, 2796, 1712 (C═O), 1637 (C═O), 1591, 1517, 1438, 1313 (C—O—C), 1261, 1238, 1118 (C—O—C), 887, 840, 777
MS (ESI(+) 70V, m/z): 469.2 ([M+H]+, base peak)
Anal. Calcd. for C26H29ClN2O4: C, 66.59; H, 6.23; N, 5.97. Found: C, 66.48; H, 6.67; N, 5.93.
The compound VI-3 and the compound XI-5 are subjected to the same procedure as preparation of I-1 to give white solid I-31, with yield 44% and mp 193-195° C.
1H-NMR (500 MHz, CDCl3), δ (ppm): 7.70˜7.72/7.63˜7.64 (2H, d/d, ArH19,19), 7.02˜7.03/6.38˜6.39 (2H, m/m, ArH22,22), 6.94˜6.96/6.82˜6.84 (2H, dd/dd, ArH20,20), 6.73/6.67 (2H, s/s, ArH8,8), 6.67/6.60 (2H, s/s, ArH5,5), 5.69˜5.72/5.37˜5.40 (2H, dd/dd, H1,1), 4.87˜4.90/4.57˜4.60 (2H, dd/dd, H16,16), 4.81˜4.84/4.22˜4.26 (2H, m/m, H3,3), 3.28, 3.85˜3.88 (18H, s, OCH3, OCH3), 3.36˜3.41 (1H, m, H3′), 2.64˜3.13 (17H3′, H9,9,9′,9′, H17,17,17′,17′, H4,4,4′,4′, H11,11′, H14,14′), 2.46˜2.58 (4H, m, H11,11′, H14,14′), 1.61˜1.79 (8H, m, H12,12,12′,12′, H13,13,13′,13′)
IR (cm−1): 3446, 2960, 2933, 2796, 1701 (C═O), 1637 (C═O), 1596, 1515, 1442, 1282, 1253 (C—O—C), 1114, 1022 (C—O—C), 837, 775
MS (ESI(+) 70V, m/z): 465.2 ([M+H]+, base peak)
Anal. Calcd. for C27H32N2O5: C, 69.81; H, 6.94; N, 6.03. Found: C, 70.04; H, 6.96; N, 5.90.
The experiment test tubes are divided into total binding tubes and non-specific binding tubes, and several groups of sample tubes added with competitive ligand in different concentrations are provided. The total binding tube is added with expressed membrane receptor protein equivalent to 20 μg and [3H] diprenorphine (0.5 nM) (1.44 Pbq/mol broad spectrum opioid antagonist, Amersham), the corresponding non-specific binding tubes are further added with 1 μM Naloxone (broad spectrum opioid antagonist, Sigma), the sample tubes are added with different concentrations compounds which are to be screened, the final volume is regulated to 100 μl with 50 mM Tris(Amresco)-HCl (pH 7.4). Incubation is performed at 30° C. for 30 min, and the tubes are placed into ice water to stop reaction. Negative pressure filter is performed in Millipore sample collector via GF/(Whatman) glass fiber filter paper. Ice cold 50 mM Tris-HCl (pH 7.4) is used to wash the filter paper for three times, each for 4 ml; Dry the filter paper and place it in 0.5 ml Eppendorff tube, and add 0.5 ml of lipophilic scintillator liquid (Reagent No. 1 Factory Of Shanghai Chemical Reagent Co. Ltd). Beckman LS 6500 multifunctional liquid scintillation counter is adopted for measuring radiation intensity, calculating inhibition rate is calculated, each concentration has three duplicated tubes, and each tube is independently tested for 3-4 times.
IC50 value is calculated by software Prism 4.0.
Ki=IC50/(1+[L]/Kd), ([L] is the concentration of added marked ligand, and Kd is equilibrium dissociation constant of radioligand).
Pharmacological test results of partial compounds are as below:
arepresents inhibition rate of the compound at 1 × 10−5M.
arepresents inhibition rate of medicine at 1 × 10−6M.
a represents inhibition rate of medicine at 1×10−6M.
Analgesic efficacy of the subject compound is determined by using model derived from mice hot plate method and mice writhing method (Methodology of Pharmacological Experiment, edition II, Xu Shuyun, People Medical Publishing Company, 1991).
Mice Writhing Assay
Compared with morphine, compound I-1 and I-6 have powerful analgesic efficacy, and their analgesic activities for mice hot plate method and mice writhing method are shown in Table 4.
Acute toxicity of compound I-6 is determined according to Methodology of Pharmacological Experiment, edition II, Xu Shuyun (People's Medical Publishing House, 1991), and An Introduction of the Assessment for Novel Drugs, edition II, Qin Boyi (People's Medical Publishing House, 1999).
Kunming mice (body weight 18-22 g, female 6 weeks old, male 4-5 weeks) are provided, randomly divided into groups each having 20 mice (half female, half male). The mice are subjected to adaptive feeding for 1-2 days before administration. Compound I-6 is administered peritoneally for 4 dosage groups, 60 mg/kg, 50 mg/kg, 40 mg/kg, and 30 mg/kg. The mice are normally fed after administration, their conditions, such as drinking, feeding, excreting, activity, and hair color, are observed everyday, their body weights are weighed every other day, and the observation lasts for two weeks.
The experiment result shows that peritoneal administration at 30 mg/kg has no influence on drinking, feeding, excreting, activities, and hair color of mice. The LD50 value of the compound I-6 is 40.147 (36.805-43.792) mg/kg.
Kuming mice (18-20 g, male) are selected for test, and divided into physiological saline group, morphine group, and I-6 group.
physiological saline group: subcutaneous administration, 0.2 mL for each mice.
Morphine group:
Hot plate method in mice is adopted as model, administration lasts for 9 days, analgesic effects before and after administration are determined every day, and if analgesic effect is attenuated after continuous administration of 3 days, the drug concentration will be increased, and if analgesic effect don't change, the drug concentration will not be changed.
Compared with morphine, the compound I-6 does not produce significant tolerance phenomena in mice test. The result is shown in the following figure, morphine has attenuated analgesic effect from Day 2, and has no significant analgesic effect at dosage of 7 mg/kg on Day 3, and higher dosage is required to restore its analgesic effect. While the compound I-6 has no such phenomena. The result is shown in
Kuming mice (18-20 g, male) are selected, and divided into physiological saline group, morphine group, and I-6 group.
physiological saline group: subcutaneous injection, 0.2 mL for each mice, continuous administration for 10 days.
morphine group: subcutaneous injection, administration according to an escalating dose schedule, 20, 40, 60, 80, 100 mg/kg, continuous administration for 10 days, two injections per day at 8 hours interval, administration with escalating concentration, and 100 mg/kg is maintained from the fifth injection until Day 10.
I-6 group: subcutaneous injection, administration according to an escalating dose schedule, 50, 100, 150, 200, 300 μg/kg, continuous administration for 10 days, two injections per day at 8 hours interval, administration with escalating concentration, and 300 μg/kg is maintained from the fifth injection until Day 10.
2 hours after the end administration on the Day 10, each group is peritoneally administered with Naloxone 3 mg/kg, and jump times and weight reduction of mice within 20 min in each group are observed.
Compared with jump times and body weight reduction of mice caused by Naloxone-induced morphine physical dependence, the compound I-6 causes no physical dependence like morphine after continuous administration. As shown in
Kuming mice (18-20 g, male) are selected and divided into physiological saline group, morphine group, and I-6+morphine group.
physiological saline group: subcutaneous injection, 0.2 mL for each mouse, continuous administration for 10 days.
morphine group: subcutaneous injection, administration according to an escalating dose schedule, 20, 40, 60, 80, 100 mg/kg, continuous administration for 10 days, two injections per day at 8 hours interval, administration with escalating concentration, and 100 mg/kg is maintained from the fifth injection until Day 10.
I-6+morphine group: subcutaneous injection of morphine according to 20, 40, 60, 80, 100 mg/kg, continuous administration for 10 days, two injections per day at 8 hours interval, administration with escalating concentration, and 100 mg/kg is maintained from the fifth injection until Day 10; 300 μg/kg of compound I-6 is administered peritonally 10 min before administration of morphine every day.
2 hours after the end administration on Day 10, each group is peritoneally administered with Naloxone 3 mg/kg, and jump times and weight reduction of mice within 20 min in each group are observed.
The result shows that the compound I-6 can resist physical dependence caused by morphine. By using jump times of morphine physical dependence mice after Naloxone-induced as index, peritoneal administration of the compound I-6 300 μg/kg 10 min before administration of morphine every day can significantly reduce jump times of Naloxone-induced mice. The result is shown in
The symbol of the compound in the pharmacological experiment is same as that of the compound in the embodiment.
| Number | Date | Country | Kind |
|---|---|---|---|
| 200610088349.0 | Jul 2006 | CN | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN2007/002115 | 7/10/2007 | WO | 00 | 3/17/2009 |
