TWI691332B - 噻唑烷酮化合物及其用途 - Google Patents
噻唑烷酮化合物及其用途 Download PDFInfo
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- TWI691332B TWI691332B TW106107199A TW106107199A TWI691332B TW I691332 B TWI691332 B TW I691332B TW 106107199 A TW106107199 A TW 106107199A TW 106107199 A TW106107199 A TW 106107199A TW I691332 B TWI691332 B TW I691332B
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- mmol
- thiazolidin
- fluorophenyl
- hours
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 207
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 28
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- 108090000137 Opioid Receptors Proteins 0.000 claims abstract description 21
- -1 C 1-6 polyhaloalkoxy Chemical group 0.000 claims description 125
- 125000001072 heteroaryl group Chemical group 0.000 claims description 36
- 125000003118 aryl group Chemical group 0.000 claims description 35
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 29
- 125000003545 alkoxy group Chemical group 0.000 claims description 25
- 229910052736 halogen Inorganic materials 0.000 claims description 22
- 150000002367 halogens Chemical class 0.000 claims description 22
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 21
- 208000002193 Pain Diseases 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 230000036407 pain Effects 0.000 claims description 16
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 15
- 208000035475 disorder Diseases 0.000 claims description 14
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 13
- 125000003282 alkyl amino group Chemical group 0.000 claims description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 11
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 10
- 125000006684 polyhaloalkyl group Polymers 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 229910052727 yttrium Inorganic materials 0.000 claims description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 101710178223 Mu-type opioid receptor Proteins 0.000 claims description 5
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- RYIDHLJADOKWFM-MAODMQOUSA-N Samidorphan Chemical compound N1([C@@H]2CC3=CC=C(C(=C3[C@@]3([C@]2(CCC(=O)C3)O)CC1)O)C(=O)N)CC1CC1 RYIDHLJADOKWFM-MAODMQOUSA-N 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- PQKHESYTSKMWFP-WZJCLRDWSA-N beta-Funaltrexamine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]1(O)CC[C@H]3NC(=O)/C=C/C(=O)OC)CN2CC1CC1 PQKHESYTSKMWFP-WZJCLRDWSA-N 0.000 claims description 5
- RAURUSFBVQLAPW-DNIKMYEQSA-N clocinnamox Chemical compound N1([C@@H]2CC3=CC=C(C=4O[C@@H]5[C@](C3=4)([C@]2(CCC5=O)NC(=O)\C=C\C=2C=CC(Cl)=CC=2)CC1)O)CC1CC1 RAURUSFBVQLAPW-DNIKMYEQSA-N 0.000 claims description 5
- INUCRGMCKDQKNA-CEMLEFRQSA-N cyprodime Chemical compound N1([C@@H]2CC=3C=CC=C(C=3[C@@]3([C@]2(CCC(=O)C3)OC)CC1)OC)CC1CC1 INUCRGMCKDQKNA-CEMLEFRQSA-N 0.000 claims description 5
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 5
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- DQCKKXVULJGBQN-XFWGSAIBSA-N naltrexone Chemical compound N1([C@@H]2CC3=CC=C(C=4O[C@@H]5[C@](C3=4)([C@]2(CCC5=O)O)CC1)O)CC1CC1 DQCKKXVULJGBQN-XFWGSAIBSA-N 0.000 claims description 5
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- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 3
- 206010058019 Cancer Pain Diseases 0.000 claims description 3
- WJBLNOPPDWQMCH-MBPVOVBZSA-N Nalmefene Chemical compound N1([C@@H]2CC3=CC=C(C=4O[C@@H]5[C@](C3=4)([C@]2(CCC5=C)O)CC1)O)CC1CC1 WJBLNOPPDWQMCH-MBPVOVBZSA-N 0.000 claims description 3
- 208000021302 gastroesophageal reflux disease Diseases 0.000 claims description 3
- 229960005297 nalmefene Drugs 0.000 claims description 3
- AJPSBXJNFJCCBI-YOHUGVJRSA-N naloxonazine Chemical compound C([C@@H](N(CC1)CC=C)[C@]2(O)CC\C3=N/N=C4/[C@H]5[C@]67CCN(CC=C)[C@@H]([C@@]7(CC4)O)CC4=CC=C(C(O5)=C46)O)C4=CC=C(O)C5=C4[C@@]21[C@H]3O5 AJPSBXJNFJCCBI-YOHUGVJRSA-N 0.000 claims description 3
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- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 4
- UZHSEJADLWPNLE-GRGSLBFTSA-N naloxone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(O)C2=C5[C@@]13CCN4CC=C UZHSEJADLWPNLE-GRGSLBFTSA-N 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000004431 deuterium atom Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 20
- 229910052805 deuterium Inorganic materials 0.000 abstract description 3
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- 238000003818 flash chromatography Methods 0.000 description 115
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- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 108
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 106
- 239000000243 solution Substances 0.000 description 104
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 99
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- 125000004494 ethyl ester group Chemical group 0.000 description 27
- 230000002829 reductive effect Effects 0.000 description 27
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- 238000010438 heat treatment Methods 0.000 description 22
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- 150000004702 methyl esters Chemical class 0.000 description 16
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- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 14
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 14
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- 230000000694 effects Effects 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
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- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 7
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical compound CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 description 6
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- 238000002360 preparation method Methods 0.000 description 5
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- GFGOYQKOFLPPHZ-UHFFFAOYSA-N methyl 2-(4-amino-3-methylphenyl)acetate Chemical compound COC(=O)CC1=CC=C(N)C(C)=C1 GFGOYQKOFLPPHZ-UHFFFAOYSA-N 0.000 description 4
- FNQVRYQDFZPHKM-UHFFFAOYSA-N methyl 2-[4-[2-(4-fluorophenyl)-4-oxo-1,3-thiazolidin-3-yl]-3-methylphenyl]acetate Chemical compound FC1=CC=C(C=C1)C1SCC(N1C1=C(C=C(C=C1)CC(=O)OC)C)=O FNQVRYQDFZPHKM-UHFFFAOYSA-N 0.000 description 4
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- XDVMMGZAIOABPW-UHFFFAOYSA-N methyl 4-[2-(4-chlorophenyl)-4-oxo-1,3-thiazolidin-3-yl]-3-methylbenzoate Chemical compound COC(C1=CC(=C(C=C1)N1C(SCC1=O)C1=CC=C(C=C1)Cl)C)=O XDVMMGZAIOABPW-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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| US20070015782A1 (en) | 2005-04-15 | 2007-01-18 | Eisai Co., Ltd. | Benzimidazole compound |
| WO2008112674A1 (en) | 2007-03-12 | 2008-09-18 | Irm Llc | Compounds and compositions as inhibitors of cannabinoid receptor 1 activity |
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- 2017-03-07 CN CN201780015438.9A patent/CN108883099B/zh active Active
- 2017-03-07 WO PCT/US2017/021033 patent/WO2017155910A1/en not_active Ceased
- 2017-03-07 AU AU2017229129A patent/AU2017229129B2/en active Active
- 2017-03-07 KR KR1020187028365A patent/KR102365673B1/ko active Active
- 2017-03-07 CA CA3015914A patent/CA3015914A1/en active Pending
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- 2017-03-07 EP EP17763849.1A patent/EP3426246B1/en active Active
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| EP3426246A4 (en) | 2019-08-07 |
| NZ745619A (en) | 2024-09-27 |
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| US10544113B2 (en) | 2020-01-28 |
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| EP3426246A1 (en) | 2019-01-16 |
| AU2017229129A1 (en) | 2018-09-06 |
| CN108883099B (zh) | 2021-09-28 |
| CN108883099A (zh) | 2018-11-23 |
| EP3426246B1 (en) | 2024-05-01 |
| CA3015914A1 (en) | 2017-09-14 |
| KR102365673B1 (ko) | 2022-02-23 |
| TW201735921A (zh) | 2017-10-16 |
| US20170253569A1 (en) | 2017-09-07 |
| KR20180119164A (ko) | 2018-11-01 |
| WO2017155910A1 (en) | 2017-09-14 |
| JP7132849B2 (ja) | 2022-09-07 |
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