JP2013522363A5 - - Google Patents
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- Publication number
- JP2013522363A5 JP2013522363A5 JP2013501347A JP2013501347A JP2013522363A5 JP 2013522363 A5 JP2013522363 A5 JP 2013522363A5 JP 2013501347 A JP2013501347 A JP 2013501347A JP 2013501347 A JP2013501347 A JP 2013501347A JP 2013522363 A5 JP2013522363 A5 JP 2013522363A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridyl
- compound according
- halo
- thienyl
- compound
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims description 46
- 125000001475 halogen functional group Chemical group 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- -1 4-furyl Chemical group 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 208000035475 disorder Diseases 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 6
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 6
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 208000027520 Somatoform disease Diseases 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 208000027753 pain disease Diseases 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 125000006239 protecting group Chemical group 0.000 claims description 4
- 208000028698 Cognitive impairment Diseases 0.000 claims description 3
- 208000019022 Mood disease Diseases 0.000 claims description 3
- 206010066218 Stress Urinary Incontinence Diseases 0.000 claims description 3
- 208000010877 cognitive disease Diseases 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000002560 therapeutic procedure Methods 0.000 claims description 3
- KNOYHJOPRUTPSQ-QHCPKHFHSA-N (4s)-5-amino-5-oxo-4-[3-[4-(4-phenylphenyl)phenyl]propanoylamino]pentanoic acid Chemical compound C1=CC(CCC(=O)N[C@@H](CCC(O)=O)C(=O)N)=CC=C1C1=CC=C(C=2C=CC=CC=2)C=C1 KNOYHJOPRUTPSQ-QHCPKHFHSA-N 0.000 claims description 2
- 208000017194 Affective disease Diseases 0.000 claims description 2
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims description 2
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 2
- 208000008035 Back Pain Diseases 0.000 claims description 2
- 206010008874 Chronic Fatigue Syndrome Diseases 0.000 claims description 2
- 208000001640 Fibromyalgia Diseases 0.000 claims description 2
- 208000008930 Low Back Pain Diseases 0.000 claims description 2
- 208000008589 Obesity Diseases 0.000 claims description 2
- 229940121991 Serotonin and norepinephrine reuptake inhibitor Drugs 0.000 claims description 2
- 230000007131 anti Alzheimer effect Effects 0.000 claims description 2
- 230000001773 anti-convulsant effect Effects 0.000 claims description 2
- 230000001430 anti-depressive effect Effects 0.000 claims description 2
- 230000000648 anti-parkinson Effects 0.000 claims description 2
- 239000001961 anticonvulsive agent Substances 0.000 claims description 2
- 239000000935 antidepressant agent Substances 0.000 claims description 2
- 229940005513 antidepressants Drugs 0.000 claims description 2
- 229960003965 antiepileptics Drugs 0.000 claims description 2
- 239000000939 antiparkinson agent Substances 0.000 claims description 2
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 230000001684 chronic effect Effects 0.000 claims description 2
- 201000010099 disease Diseases 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 230000009977 dual effect Effects 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 230000009245 menopause Effects 0.000 claims description 2
- 208000029766 myalgic encephalomeyelitis/chronic fatigue syndrome Diseases 0.000 claims description 2
- 208000004296 neuralgia Diseases 0.000 claims description 2
- 208000021722 neuropathic pain Diseases 0.000 claims description 2
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims description 2
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims description 2
- 239000002767 noradrenalin uptake inhibitor Substances 0.000 claims description 2
- 229940127221 norepinephrine reuptake inhibitor Drugs 0.000 claims description 2
- 235000020824 obesity Nutrition 0.000 claims description 2
- 239000003402 opiate agonist Substances 0.000 claims description 2
- 239000003401 opiate antagonist Substances 0.000 claims description 2
- 201000008482 osteoarthritis Diseases 0.000 claims description 2
- 229940124834 selective serotonin reuptake inhibitor Drugs 0.000 claims description 2
- 239000012896 selective serotonin reuptake inhibitor Substances 0.000 claims description 2
- 239000003775 serotonin noradrenalin reuptake inhibitor Substances 0.000 claims description 2
- 239000003195 sodium channel blocking agent Substances 0.000 claims description 2
- 230000002889 sympathetic effect Effects 0.000 claims description 2
- 208000024891 symptom Diseases 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 229940124597 therapeutic agent Drugs 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 230000001457 vasomotor Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 3
- 229940125794 sodium channel blocker Drugs 0.000 claims 1
- 241000124008 Mammalia Species 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 0 *c(c(*)c1*)c(*)c(*)c1OCC1/C=C/C/C=C/CC1C1CCNCC1 Chemical compound *c(c(*)c1*)c(*)c(*)c1OCC1/C=C/C/C=C/CC1C1CCNCC1 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 208000013403 hyperactivity Diseases 0.000 description 1
- 230000000966 norepinephrine reuptake Effects 0.000 description 1
- 230000000697 serotonin reuptake Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31609010P | 2010-03-22 | 2010-03-22 | |
| US61/316,090 | 2010-03-22 | ||
| PCT/US2011/029138 WO2011119461A1 (en) | 2010-03-22 | 2011-03-21 | 1-(2-phenoxymethylheteroaryl)piperidine and piperazine compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013522363A JP2013522363A (ja) | 2013-06-13 |
| JP2013522363A5 true JP2013522363A5 (cg-RX-API-DMAC7.html) | 2014-02-13 |
| JP5769348B2 JP5769348B2 (ja) | 2015-08-26 |
Family
ID=44211953
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013501347A Expired - Fee Related JP5769348B2 (ja) | 2010-03-22 | 2011-03-21 | １−（２−フェノキシメチルヘテロアリール）ピペリジン化合物および１−（２−フェノキシメチルヘテロアリール）ピペラジン化合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US8530663B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2550252B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5769348B2 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2543064T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2011119461A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2358674T3 (pl) * | 2008-11-14 | 2013-06-28 | Theravance Inc | Sposób otrzymywania związków 4-[2-(2-fluorofenoksymetylo)fenylo]piperydyny |
| US8778949B2 (en) | 2010-01-11 | 2014-07-15 | Theravance Biopharma R&D Ip, Llc | 1-(2-phenoxymethylphenyl)piperazine compounds |
| US9181185B2 (en) | 2011-10-31 | 2015-11-10 | Purdue Pharma L.P. | Heteroaryl compounds as sodium channel blockers |
| US20210387968A1 (en) * | 2019-01-31 | 2021-12-16 | Ideaya Biosciences, Inc. | Heteroarylmethylene derivatives as dna polymerase theta inhibitors |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1422263A (en) | 1973-01-30 | 1976-01-21 | Ferrosan As | 4-phenyl-piperidine compounds |
| DE2549999A1 (de) | 1975-11-07 | 1977-05-12 | Boehringer Mannheim Gmbh | Piperidin-derivate und verfahren zu ihrer herstellung |
| IL56369A (en) | 1978-01-20 | 1984-05-31 | Erba Farmitalia | Alpha-phenoxybenzyl propanolamine derivatives,their preparation and pharmaceutical compositions comprising them |
| US4179563A (en) * | 1978-05-19 | 1979-12-18 | Warner-Lambert Company | 3-Aryloxy-substituted-aminopyridines and methods for their production |
| US4198417A (en) | 1979-01-10 | 1980-04-15 | American Hoechst Corporation | Phenoxyphenylpiperidines |
| EP0190496A3 (en) | 1984-12-13 | 1987-05-27 | Beecham Group Plc | Piperidine derivatives having a gastro-intestinal activity |
| DE3541097A1 (de) * | 1985-11-21 | 1987-05-27 | Miles Lab | Verwendung von thiophenen als ph indikatoren insbesondere in einem nicht-enzymatischen glukosetest |
| US4956388A (en) | 1986-12-22 | 1990-09-11 | Eli Lilly And Company | 3-aryloxy-3-substituted propanamines |
| DE3835291A1 (de) | 1988-04-19 | 1989-11-02 | Bayer Ag | 1,3-disubstituierte pyrrolidine |
| GB9324018D0 (en) | 1993-11-23 | 1994-01-12 | Merck Sharp & Dohme | Therapeutic agents |
| US6518284B2 (en) | 1998-11-18 | 2003-02-11 | Faes, Fabrica Espanola De Productos Quimicos Y Farmaceuticos S.A. | 4-substituted piperidines |
| US6630504B2 (en) | 2000-08-31 | 2003-10-07 | Pfizer Inc. | Phenoxyphenylheterocyclyl derivatives as SSRIs |
| US7294637B2 (en) | 2000-09-11 | 2007-11-13 | Sepracor, Inc. | Method of treating addiction or dependence using a ligand for a monamine receptor or transporter |
| UA81749C2 (uk) | 2001-10-04 | 2008-02-11 | Х. Луннбек А/С | Фенілпіперазинові похідні як інгібітори зворотного захоплення серотоніну |
| AU2003269923A1 (en) | 2002-08-23 | 2004-03-11 | Eli Lilly And Company | 2- (phenoxymethyl)- and 2- (phenylthiomethyl)-morpholine derivatives for use as selective norepinephrine reuptake inhibitors |
| SI1635828T1 (sl) | 2003-04-04 | 2008-08-31 | Lundbeck & Co As H | Derivati 4-(2-feniloksifenil)-piperidina ali-1,2,3,6-tetrahidropiridina kot inhibitorji ponovnega privzema serotonina |
| ES2305776T3 (es) | 2003-06-17 | 2008-11-01 | Pfizer Inc. | Derivados de n-pirrolidin-3-il-amida como inhibidores de la re-captacion de serotonina y noradrenalina. |
| BRPI0506844A (pt) | 2004-01-13 | 2007-06-12 | Pfizer | derivados de piperazina que apresentam atividade como inibidores da reabsorção de serotonina noradrenalina |
| US20070072859A1 (en) | 2004-03-05 | 2007-03-29 | Eli Lilly And Company | Pharmaceutical compounds |
| WO2005105763A1 (en) | 2004-04-30 | 2005-11-10 | Warner-Lambert Company Llc | Substituted morpholine compounds for the treatment of central nervous system disorders |
| EP1745033A4 (en) * | 2004-05-08 | 2009-08-26 | Neurogen Corp | 2-ARYLPYRIMIDINES DISUBSTITUTED IN 4,5 |
| US20100120858A1 (en) | 2006-08-23 | 2010-05-13 | Pfizer Inc. | Piperidine Derivatives |
| US8026257B2 (en) | 2007-07-11 | 2011-09-27 | Bristol-Myers Squibb Company | Substituted heterocyclic ethers and their use in CNS disorders |
| TW200918521A (en) * | 2007-08-31 | 2009-05-01 | Astrazeneca Ab | Heterocyclic amides and methods of use thereof |
| WO2009081259A1 (en) | 2007-12-21 | 2009-07-02 | Pfizer Inc. | Phenoxy-pyridyl derivatives |
| BRPI0914891A2 (pt) * | 2008-06-20 | 2015-11-24 | Metabolex Inc | agonistas de aril gpr119 e usos dos mesmos |
| PL2358674T3 (pl) | 2008-11-14 | 2013-06-28 | Theravance Inc | Sposób otrzymywania związków 4-[2-(2-fluorofenoksymetylo)fenylo]piperydyny |
| EP2427190B1 (en) * | 2009-05-08 | 2013-09-18 | Tetraphase Pharmaceuticals, Inc. | 8-aza tetracycline compounds |
-
2011
- 2011-03-21 EP EP20110714878 patent/EP2550252B1/en not_active Not-in-force
- 2011-03-21 ES ES11714878.3T patent/ES2543064T3/es active Active
- 2011-03-21 WO PCT/US2011/029138 patent/WO2011119461A1/en not_active Ceased
- 2011-03-21 US US13/052,273 patent/US8530663B2/en not_active Expired - Fee Related
- 2011-03-21 JP JP2013501347A patent/JP5769348B2/ja not_active Expired - Fee Related
-
2013
- 2013-08-09 US US13/963,255 patent/US20130324550A1/en not_active Abandoned
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