JP2006522775A5 - - Google Patents
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- Publication number
- JP2006522775A5 JP2006522775A5 JP2006505540A JP2006505540A JP2006522775A5 JP 2006522775 A5 JP2006522775 A5 JP 2006522775A5 JP 2006505540 A JP2006505540 A JP 2006505540A JP 2006505540 A JP2006505540 A JP 2006505540A JP 2006522775 A5 JP2006522775 A5 JP 2006522775A5
- Authority
- JP
- Japan
- Prior art keywords
- het
- group
- alkyl
- phenyl
- imidazol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- -1 phenyloxy, phenylcarbonyloxy Chemical group 0.000 claims 14
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004432 carbon atom Chemical group C* 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 7
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 6
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 125000006684 polyhaloalkyl group Polymers 0.000 claims 5
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 239000000825 pharmaceutical preparation Substances 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 208000019901 Anxiety disease Diseases 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 3
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 3
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000000335 thiazolyl group Chemical group 0.000 claims 3
- 208000020401 Depressive disease Diseases 0.000 claims 2
- 125000000815 N-oxide group Chemical group 0.000 claims 2
- 208000012902 Nervous system disease Diseases 0.000 claims 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 208000015114 central nervous system disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000003884 phenylalkyl group Chemical group 0.000 claims 2
- 125000004193 piperazinyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- XESIYKHUDOXYHW-UHFFFAOYSA-N 1-[4-(1-benzylimidazol-2-yl)-4-phenylpiperidin-1-yl]-2-methoxyethanone Chemical compound C1CN(C(=O)COC)CCC1(C=1C=CC=CC=1)C1=NC=CN1CC1=CC=CC=C1 XESIYKHUDOXYHW-UHFFFAOYSA-N 0.000 claims 1
- KKKDZZRICRFGSD-UHFFFAOYSA-N 1-benzylimidazole Chemical compound C1=CN=CN1CC1=CC=CC=C1 KKKDZZRICRFGSD-UHFFFAOYSA-N 0.000 claims 1
- CTISCGFKPGVCBI-UHFFFAOYSA-N 2-[4-(1-benzylimidazol-2-yl)-4-phenylpiperidin-1-yl]-1,3-thiazole Chemical compound C1=CN=C(C2(CCN(CC2)C=2SC=CN=2)C=2C=CC=CC=2)N1CC1=CC=CC=C1 CTISCGFKPGVCBI-UHFFFAOYSA-N 0.000 claims 1
- MJWJGPUAWYZONC-UHFFFAOYSA-N 2-[4-phenyl-4-[1-(1-phenylethyl)imidazol-2-yl]piperidin-1-yl]-1,3-benzoxazole Chemical compound C1=CN=C(C2(CCN(CC2)C=2OC3=CC=CC=C3N=2)C=2C=CC=CC=2)N1C(C)C1=CC=CC=C1 MJWJGPUAWYZONC-UHFFFAOYSA-N 0.000 claims 1
- TXWOTCVSUZXJMH-UHFFFAOYSA-N 2-methoxy-1-[4-phenyl-4-[1-(1-phenylethyl)imidazol-2-yl]piperidin-1-yl]ethanone Chemical compound C1CN(C(=O)COC)CCC1(C=1C=CC=CC=1)C1=NC=CN1C(C)C1=CC=CC=C1 TXWOTCVSUZXJMH-UHFFFAOYSA-N 0.000 claims 1
- FBLAYKAWVSYTGT-UHFFFAOYSA-N 4-(1-benzylimidazol-2-yl)-n,4-diphenylpiperidine-1-sulfonamide Chemical compound C1CC(C=2C=CC=CC=2)(C=2N(C=CN=2)CC=2C=CC=CC=2)CCN1S(=O)(=O)NC1=CC=CC=C1 FBLAYKAWVSYTGT-UHFFFAOYSA-N 0.000 claims 1
- DTIMTKCIDGMMKY-UHFFFAOYSA-N 4-[[2-(1-benzoyl-4-phenylpiperidin-4-yl)imidazol-1-yl]methyl]-2-methylbenzoic acid Chemical compound C1=C(C(O)=O)C(C)=CC(CN2C(=NC=C2)C2(CCN(CC2)C(=O)C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 DTIMTKCIDGMMKY-UHFFFAOYSA-N 0.000 claims 1
- KIUPRXNMBOSLIU-UHFFFAOYSA-N 4-[[2-[1-(1,3-benzoxazol-2-yl)-4-phenylpiperidin-4-yl]imidazol-1-yl]methyl]-2-methylbenzoic acid Chemical compound C1=C(C(O)=O)C(C)=CC(CN2C(=NC=C2)C2(CCN(CC2)C=2OC3=CC=CC=C3N=2)C=2C=CC=CC=2)=C1 KIUPRXNMBOSLIU-UHFFFAOYSA-N 0.000 claims 1
- CFEYWAMCEXSNKC-UHFFFAOYSA-N 4-[[2-[1-(2-methoxyacetyl)-4-phenylpiperidin-4-yl]imidazol-1-yl]methyl]-2-methylbenzoic acid Chemical compound C1CN(C(=O)COC)CCC1(C=1C=CC=CC=1)C1=NC=CN1CC1=CC=C(C(O)=O)C(C)=C1 CFEYWAMCEXSNKC-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 208000030814 Eating disease Diseases 0.000 claims 1
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- DMVZSSRQHPZHFZ-UHFFFAOYSA-N [4-(1-benzylimidazol-2-yl)-4-phenylpiperidin-1-yl]-(3,5-dimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C(=O)N2CCC(CC2)(C=2N(C=CN=2)CC=2C=CC=CC=2)C=2C=CC=CC=2)=C1 DMVZSSRQHPZHFZ-UHFFFAOYSA-N 0.000 claims 1
- XHGVOFUYLQFSIW-UHFFFAOYSA-N [4-(1-benzylimidazol-2-yl)-4-phenylpiperidin-1-yl]-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)N(CC1)CCC1(C=1C=CC=CC=1)C1=NC=CN1CC1=CC=CC=C1 XHGVOFUYLQFSIW-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 230000001430 anti-depressive effect Effects 0.000 claims 1
- 230000000561 anti-psychotic effect Effects 0.000 claims 1
- 239000000935 antidepressant agent Substances 0.000 claims 1
- 229940005513 antidepressants Drugs 0.000 claims 1
- 230000036506 anxiety Effects 0.000 claims 1
- 239000002249 anxiolytic agent Substances 0.000 claims 1
- 230000000949 anxiolytic effect Effects 0.000 claims 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 230000003001 depressive effect Effects 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- QAWTYRYXDYHQNU-UHFFFAOYSA-N diazathiane Chemical group NSN QAWTYRYXDYHQNU-UHFFFAOYSA-N 0.000 claims 1
- 235000014632 disordered eating Nutrition 0.000 claims 1
- 125000005883 dithianyl group Chemical group 0.000 claims 1
- IDNSINQXOXDMHW-UHFFFAOYSA-N ethyl 4-(1-benzylimidazol-2-yl)-4-phenylpiperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1(C=1C=CC=CC=1)C1=NC=CN1CC1=CC=CC=C1 IDNSINQXOXDMHW-UHFFFAOYSA-N 0.000 claims 1
- AZPCCLQAOVOOKT-UHFFFAOYSA-N ethyl 4-phenyl-4-[1-(1-phenylethyl)imidazol-2-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1(C=1C=CC=CC=1)C1=NC=CN1C(C)C1=CC=CC=C1 AZPCCLQAOVOOKT-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000005067 haloformyl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000002632 imidazolidinyl group Chemical group 0.000 claims 1
- 125000002636 imidazolinyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- JXUWRZZEVUREMV-UHFFFAOYSA-N phenyl-[4-phenyl-4-[1-(1-phenylethyl)imidazol-2-yl]piperidin-1-yl]methanone Chemical compound C1=CN=C(C2(CCN(CC2)C(=O)C=2C=CC=CC=2)C=2C=CC=CC=2)N1C(C)C1=CC=CC=C1 JXUWRZZEVUREMV-UHFFFAOYSA-N 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 claims 1
- 125000002755 pyrazolinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000001422 pyrrolinyl group Chemical group 0.000 claims 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP0303879 | 2003-04-11 | ||
| PCT/EP2004/050492 WO2004089372A1 (en) | 2003-04-11 | 2004-04-08 | Substituted 4-phenyl-4-`1h-imidazol-2-yl !-piperidine derivatives and their use as selective non-peptide delta opioid agonists with antidepressant and anxiolytic activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006522775A JP2006522775A (ja) | 2006-10-05 |
| JP2006522775A5 true JP2006522775A5 (enExample) | 2007-06-07 |
Family
ID=33154992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006505540A Withdrawn JP2006522775A (ja) | 2003-04-11 | 2004-04-08 | 置換された４−フェニル−４−’１ｈ−イミダゾール−２−イル！−ピペリジン誘導体および抗抑鬱および不安緩解活性を有する選択性非ペプチドデルタオピオイドアゴニストとしてのそれらの使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20060287345A1 (enExample) |
| EP (1) | EP1615644B1 (enExample) |
| JP (1) | JP2006522775A (enExample) |
| AR (1) | AR044010A1 (enExample) |
| AT (1) | ATE353649T1 (enExample) |
| AU (1) | AU2004228960A1 (enExample) |
| CA (1) | CA2521186A1 (enExample) |
| CL (1) | CL2004000754A1 (enExample) |
| DE (1) | DE602004004771T2 (enExample) |
| ES (1) | ES2282858T3 (enExample) |
| TW (1) | TW200509913A (enExample) |
| WO (1) | WO2004089372A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2149370A1 (en) | 2008-07-31 | 2010-02-03 | Neuroscienze Pharmaness S.C. A R.L. | Diazabicyclic compounds and microemulsions thereof |
| IT1390848B1 (it) | 2008-07-31 | 2011-10-19 | Neuroscienze Pharmaness S C A R L | Composti farmaceutici |
| JP2011030565A (ja) * | 2009-07-06 | 2011-02-17 | Yokohama City Univ | 社会的隔離モデル動物 |
| IT1396951B1 (it) | 2009-12-18 | 2012-12-20 | Neuroscienze Pharmaness S C A R L | Composti farmaceutici |
| JP2016519161A (ja) * | 2013-05-24 | 2016-06-30 | アルカームス ファーマ アイルランド リミテッド | モルファン及びモルフィナン類似物及び使用の方法 |
| EP3974430A1 (en) | 2015-03-17 | 2022-03-30 | Nippon Chemiphar Co., Ltd. | Morphinan derivative |
| JPWO2018030382A1 (ja) | 2016-08-09 | 2019-06-13 | 日本ケミファ株式会社 | モルヒナン誘導体 |
| ES2981564T3 (es) | 2016-09-16 | 2024-10-09 | Nippon Chemiphar Co | Derivados de morfinano para el tratamiento de enfermedades relacionadas con agonistas de receptores delta opioides |
| MY205690A (en) * | 2018-05-01 | 2024-11-06 | Merck Sharp & Dohme Llc | Spiropiperidine allosteric modulators of nicotinic acetylcholine receptors |
| CA3158860A1 (en) | 2019-11-22 | 2021-05-27 | The Kitasato Institute | Pyrazolomorphinan derivative |
| TW202302096A (zh) | 2021-02-26 | 2023-01-16 | 學校法人東京理科大學 | 壓力關連障礙之治療或預防用醫藥組成物 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5354863A (en) * | 1992-01-21 | 1994-10-11 | G. D. Searle & Co. | Opioid agonist compounds |
| DE19805370A1 (de) * | 1997-03-14 | 1998-09-17 | Gruenenthal Gmbh | Substituierte Aminoverbindungen und ihre Verwendung als analgetisch wirksame Substanzen |
| HN1999000149A (es) * | 1998-09-09 | 2000-01-12 | Pfizer Prod Inc | Derivados de 4,4-biarilpiperidina |
| EP1038872A1 (en) * | 1999-02-22 | 2000-09-27 | Pfizer Products Inc. | 4-Phenyl-4-heteroarylpiperdine derivatives as opioid receptor ligands |
| DE19939044A1 (de) * | 1999-08-18 | 2001-03-15 | Gruenenthal Gmbh | Verwendung von Morphinanderivaten als Arzneimittel |
| SE0101767D0 (sv) * | 2001-05-18 | 2001-05-18 | Astrazeneca Ab | Novel compounds |
| WO2003039440A2 (en) * | 2001-10-15 | 2003-05-15 | Janssen Pharmaceutica N.V. | Substituted 4-phenyl-4-(1h-imidazol-2-yl)-piperidine derivatives for reducing ischaemic damage |
| PT1438304E (pt) * | 2001-10-15 | 2007-03-30 | Janssen Pharmaceutica Nv | Novos derivados 4-fenil-4-[1h-imidazolo-2-il] piperidina substituídos e sua utilização como agonistas selectivos não peptídicos de delta opióides |
-
2004
- 2004-04-07 AR ARP040101193A patent/AR044010A1/es not_active Application Discontinuation
- 2004-04-07 CL CL200400754A patent/CL2004000754A1/es unknown
- 2004-04-08 DE DE602004004771T patent/DE602004004771T2/de not_active Expired - Fee Related
- 2004-04-08 US US10/552,527 patent/US20060287345A1/en not_active Abandoned
- 2004-04-08 EP EP04726520A patent/EP1615644B1/en not_active Expired - Lifetime
- 2004-04-08 AU AU2004228960A patent/AU2004228960A1/en not_active Abandoned
- 2004-04-08 JP JP2006505540A patent/JP2006522775A/ja not_active Withdrawn
- 2004-04-08 AT AT04726520T patent/ATE353649T1/de not_active IP Right Cessation
- 2004-04-08 WO PCT/EP2004/050492 patent/WO2004089372A1/en not_active Ceased
- 2004-04-08 ES ES04726520T patent/ES2282858T3/es not_active Expired - Lifetime
- 2004-04-08 CA CA002521186A patent/CA2521186A1/en not_active Abandoned
- 2004-04-09 TW TW093109827A patent/TW200509913A/zh unknown
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