PL200238B1 - Związki triazolowe, środek farmaceutyczny i zastosowanie związków triazolowych - Google Patents
Związki triazolowe, środek farmaceutyczny i zastosowanie związków triazolowychInfo
- Publication number
- PL200238B1 PL200238B1 PL350246A PL35024600A PL200238B1 PL 200238 B1 PL200238 B1 PL 200238B1 PL 350246 A PL350246 A PL 350246A PL 35024600 A PL35024600 A PL 35024600A PL 200238 B1 PL200238 B1 PL 200238B1
- Authority
- PL
- Poland
- Prior art keywords
- methyl
- phenyl
- triazol
- sulfanyl
- propyl
- Prior art date
Links
- -1 Triazole compounds Chemical class 0.000 title claims abstract description 36
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- 108090000525 Dopamine D3 Receptors Proteins 0.000 title abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 83
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 16
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 12
- 150000002367 halogens Chemical class 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 206010012335 Dependence Diseases 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 6
- 150000003254 radicals Chemical group 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000001544 thienyl group Chemical group 0.000 claims description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- PUZSVCVWKDZFCA-UHFFFAOYSA-N 1-[2-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3,4-dihydro-1h-isoquinolin-7-yl]ethanone Chemical compound C1C2=CC(C(=O)C)=CC=C2CCN1CCCSC(N1C)=NN=C1C1=CC=C(C(F)(F)F)C=C1 PUZSVCVWKDZFCA-UHFFFAOYSA-N 0.000 claims description 3
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 claims description 3
- FUKQSDAOCLPAQG-UHFFFAOYSA-N 2-[3-[(4-methyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-7-(1,2,3,4-tetrahydroisoquinolin-1-ylsulfonyl)-3,4-dihydro-1h-isoquinoline Chemical compound CN1C(SCCCN2CC3=CC(=CC=C3CC2)S(=O)(=O)C2C3=CC=CC=C3CCN2)=NN=C1C1=CC=CN=C1 FUKQSDAOCLPAQG-UHFFFAOYSA-N 0.000 claims description 3
- VDDKRZHBIWRFCM-UHFFFAOYSA-N 2-[3-[(4-methyl-5-thiophen-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-7-(1,2,3,4-tetrahydroisoquinolin-1-ylsulfonyl)-3,4-dihydro-1h-isoquinoline Chemical compound CN1C(SCCCN2CC3=CC(=CC=C3CC2)S(=O)(=O)C2C3=CC=CC=C3CCN2)=NN=C1C=1C=CSC=1 VDDKRZHBIWRFCM-UHFFFAOYSA-N 0.000 claims description 3
- NENYEAGCYBXUCJ-UHFFFAOYSA-N 7-(3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinolin-2-ylsulfonyl)-2-[3-[(4-methyl-5-phenyl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3,4-dihydro-1h-isoquinoline Chemical compound CN1C(SCCCN2CC3=CC(=CC=C3CC2)S(=O)(=O)N2CC3CCCCC3CC2)=NN=C1C1=CC=CC=C1 NENYEAGCYBXUCJ-UHFFFAOYSA-N 0.000 claims description 3
- ZKOVSNFXAYVHNN-UHFFFAOYSA-N 7-(3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinolin-2-ylsulfonyl)-2-[3-[(4-methyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3,4-dihydro-1h-isoquinoline Chemical compound CN1C(SCCCN2CC3=CC(=CC=C3CC2)S(=O)(=O)N2CC3CCCCC3CC2)=NN=C1C1=CC=CN=C1 ZKOVSNFXAYVHNN-UHFFFAOYSA-N 0.000 claims description 3
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| DE19900811 | 1999-01-12 | ||
| PCT/EP2000/000177 WO2000042036A1 (de) | 1999-01-12 | 2000-01-12 | Triazolverbindungen mit dopamin-d3-rezeptoraffinität |
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| PL350246A1 PL350246A1 (en) | 2002-12-02 |
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| KR20030045187A (ko) * | 2000-11-14 | 2003-06-09 | 스미스클라인비이참피이엘시이 | 도파민 d₃수용체 조절제 (정신병 치료제)로서 유용한테트라히드로벤즈아제핀 유도체 |
| HU227543B1 (en) * | 2001-09-28 | 2011-08-29 | Richter Gedeon Nyrt | N-[4-(2-piperazin- and 2-piperidin-1-yl-ethyl)-cyclohexyl]-sulfon- and sulfamides, process for their preparation, their use and pharmaceutical compositions containing them |
| GB0130219D0 (en) * | 2001-12-18 | 2002-02-06 | Pfizer Ltd | Compounds for the treatment of sexual dysfunction |
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| US7314937B2 (en) * | 2002-03-21 | 2008-01-01 | Eli Lilly And Company | Non-imidazole aryl alkylamines compounds as histamine H3 receptor antagonists, preparation and therapeutic uses |
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| WO2005090320A2 (en) * | 2004-03-12 | 2005-09-29 | Wyeth | Triazole derivatives and method of using the same to treat hiv infections |
| GB0412314D0 (en) * | 2004-06-02 | 2004-07-07 | Glaxo Group Ltd | Compounds |
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