CN103517910B - 作为离子通道调节剂的吗啉-螺环哌啶酰胺 - Google Patents
作为离子通道调节剂的吗啉-螺环哌啶酰胺 Download PDFInfo
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- CN103517910B CN103517910B CN201280018832.5A CN201280018832A CN103517910B CN 103517910 B CN103517910 B CN 103517910B CN 201280018832 A CN201280018832 A CN 201280018832A CN 103517910 B CN103517910 B CN 103517910B
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- 0 C*CCC(CCCCC1)(CCCC1C1OC(CC2)(CCN2C(c2ccc(*)c(*)c2)=O)CN(*)C1)[N+](*)=[I-] Chemical compound C*CCC(CCCCC1)(CCCC1C1OC(CC2)(CCN2C(c2ccc(*)c(*)c2)=O)CN(*)C1)[N+](*)=[I-] 0.000 description 28
- VFQUGUQMEDNBER-UHFFFAOYSA-N CC(/N=C(/C)\O)=N Chemical compound CC(/N=C(/C)\O)=N VFQUGUQMEDNBER-UHFFFAOYSA-N 0.000 description 1
- DXPBAHCKZUVUHG-NTMALXAHSA-N CC(C)(C)C(O/C(/C)=N\C)=C Chemical compound CC(C)(C)C(O/C(/C)=N\C)=C DXPBAHCKZUVUHG-NTMALXAHSA-N 0.000 description 1
- IILYOUPCOLLFBV-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(CN(CC(F)(F)F)C1)OC1C(O)=[U])=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(CN(CC(F)(F)F)C1)OC1C(O)=[U])=O IILYOUPCOLLFBV-UHFFFAOYSA-N 0.000 description 1
- LRPAZOXUBHPRBM-UHFFFAOYSA-N CC(C)Oc(cc1)c(C)cc1C(N(CC1)CCC1(CN(CC(F)F)C1)OC1c(cc1)ccc1Cl)=O Chemical compound CC(C)Oc(cc1)c(C)cc1C(N(CC1)CCC1(CN(CC(F)F)C1)OC1c(cc1)ccc1Cl)=O LRPAZOXUBHPRBM-UHFFFAOYSA-N 0.000 description 1
- QXSPLPLQLJAPSM-UHFFFAOYSA-N CC(C)Oc(ccc(C(O)=O)c1)c1Cl Chemical compound CC(C)Oc(ccc(C(O)=O)c1)c1Cl QXSPLPLQLJAPSM-UHFFFAOYSA-N 0.000 description 1
- UMQXTTPXTATBGI-UHFFFAOYSA-N CC(C)Oc1ccc(C(O)=O)nc1 Chemical compound CC(C)Oc1ccc(C(O)=O)nc1 UMQXTTPXTATBGI-UHFFFAOYSA-N 0.000 description 1
- JMKOIOOSJTWRHE-UHFFFAOYSA-N CC(CC=C)(CN1CC2(CCNCC2)OC(COC)C1)F Chemical compound CC(CC=C)(CN1CC2(CCNCC2)OC(COC)C1)F JMKOIOOSJTWRHE-UHFFFAOYSA-N 0.000 description 1
- NHQHAGTUESYFRW-UHFFFAOYSA-N CC1(COC1)[N+]([O-])=O Chemical compound CC1(COC1)[N+]([O-])=O NHQHAGTUESYFRW-UHFFFAOYSA-N 0.000 description 1
- JYTLRDOVMICCLC-UHFFFAOYSA-N CC1=CCC=CC=N1 Chemical compound CC1=CCC=CC=N1 JYTLRDOVMICCLC-UHFFFAOYSA-N 0.000 description 1
- ATQUFXWBVZUTKO-UHFFFAOYSA-N CC1=CCCC1 Chemical compound CC1=CCCC1 ATQUFXWBVZUTKO-UHFFFAOYSA-N 0.000 description 1
- NBYZBSXQNJJELW-UHFFFAOYSA-N CCC(CC1)(CCN1C(C1=CC=CC=CC=CC=C1)=O)O Chemical compound CCC(CC1)(CCN1C(C1=CC=CC=CC=CC=C1)=O)O NBYZBSXQNJJELW-UHFFFAOYSA-N 0.000 description 1
- NBVLRBYCQGCKEK-UHFFFAOYSA-N CCC1=NC=C(C)OC1 Chemical compound CCC1=NC=C(C)OC1 NBVLRBYCQGCKEK-UHFFFAOYSA-N 0.000 description 1
- JZDVAJJFFPDEDR-UHFFFAOYSA-N CCC1OC(CC2)(CCN2C(c(cc2C)ccc2OC(C)C)=O)CN(CC)C1 Chemical compound CCC1OC(CC2)(CCN2C(c(cc2C)ccc2OC(C)C)=O)CN(CC)C1 JZDVAJJFFPDEDR-UHFFFAOYSA-N 0.000 description 1
- LQVWXFHNYICENT-UHFFFAOYSA-N CCN(C)CC=C Chemical compound CCN(C)CC=C LQVWXFHNYICENT-UHFFFAOYSA-N 0.000 description 1
- ZWQDGTXFYVVVNE-UHFFFAOYSA-N CCN1C(C)(C)COC(CC2)(CCN2C2(c(cc3C)ccc3OC(C)C)OCC2)C1 Chemical compound CCN1C(C)(C)COC(CC2)(CCN2C2(c(cc3C)ccc3OC(C)C)OCC2)C1 ZWQDGTXFYVVVNE-UHFFFAOYSA-N 0.000 description 1
- LWFFUGBHIDRGIR-UHFFFAOYSA-N CCS(c(cc1)c(C)cc1C(O)=O)(=O)=O Chemical compound CCS(c(cc1)c(C)cc1C(O)=O)(=O)=O LWFFUGBHIDRGIR-UHFFFAOYSA-N 0.000 description 1
- SJRJJKPEHAURKC-UHFFFAOYSA-N CN1CCOCC1 Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 1
- XXYUNCRVXKJBKV-UHFFFAOYSA-N CS(C1=COCC1)(=O)=O Chemical compound CS(C1=COCC1)(=O)=O XXYUNCRVXKJBKV-UHFFFAOYSA-N 0.000 description 1
- HHWUOZJEHMOHSE-UHFFFAOYSA-N CS(C1COCC1)(=O)=O Chemical compound CS(C1COCC1)(=O)=O HHWUOZJEHMOHSE-UHFFFAOYSA-N 0.000 description 1
- GMQPIGJXSZAXSJ-UHFFFAOYSA-N CS(N1CCCC1)(=O)=O Chemical compound CS(N1CCCC1)(=O)=O GMQPIGJXSZAXSJ-UHFFFAOYSA-N 0.000 description 1
- OISVCGZHLKNMSJ-UHFFFAOYSA-N Cc1cccc(C)n1 Chemical compound Cc1cccc(C)n1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
- LSZQMSSIUQNTDX-UHFFFAOYSA-N Cc1ccn[n]1C Chemical compound Cc1ccn[n]1C LSZQMSSIUQNTDX-UHFFFAOYSA-N 0.000 description 1
- ZCHCHJQEWYIJDQ-UHFFFAOYSA-N Cc1ncc[o]1 Chemical compound Cc1ncc[o]1 ZCHCHJQEWYIJDQ-UHFFFAOYSA-N 0.000 description 1
- QEEOVPOWJNZAIR-UHFFFAOYSA-N FC(CN(C1)CC2(CCNCC2)OC1c(cccc1)c1F)F Chemical compound FC(CN(C1)CC2(CCNCC2)OC1c(cccc1)c1F)F QEEOVPOWJNZAIR-UHFFFAOYSA-N 0.000 description 1
- GVJFGFRBRJBBOV-UHFFFAOYSA-N FC(CN(C1)CC2(CCNCC2)OC1c1ncc[o]1)F Chemical compound FC(CN(C1)CC2(CCNCC2)OC1c1ncc[o]1)F GVJFGFRBRJBBOV-UHFFFAOYSA-N 0.000 description 1
- BKDBALCSMUJSQE-UHFFFAOYSA-N OC1(CCCCC1)c(cc1)ccc1C(O)=O Chemical compound OC1(CCCCC1)c(cc1)ccc1C(O)=O BKDBALCSMUJSQE-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Otolaryngology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161452538P | 2011-03-14 | 2011-03-14 | |
| US61/452,538 | 2011-03-14 | ||
| US201161567809P | 2011-12-07 | 2011-12-07 | |
| US61/567,809 | 2011-12-07 | ||
| PCT/US2012/028882 WO2012125613A1 (en) | 2011-03-14 | 2012-03-13 | Morpholine-spirocyclic piperidine amides as modulators of ion channels |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103517910A CN103517910A (zh) | 2014-01-15 |
| CN103517910B true CN103517910B (zh) | 2016-12-14 |
Family
ID=45888492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280018832.5A Expired - Fee Related CN103517910B (zh) | 2011-03-14 | 2012-03-13 | 作为离子通道调节剂的吗啉-螺环哌啶酰胺 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US8828996B2 (enExample) |
| EP (1) | EP2686325B1 (enExample) |
| JP (1) | JP6088443B2 (enExample) |
| CN (1) | CN103517910B (enExample) |
| AU (1) | AU2012229187B2 (enExample) |
| CA (1) | CA2829803A1 (enExample) |
| ES (1) | ES2618929T3 (enExample) |
| MX (1) | MX347982B (enExample) |
| WO (1) | WO2012125613A1 (enExample) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011140425A1 (en) | 2010-05-06 | 2011-11-10 | Vertex Pharmaceuticals Incorporated | Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels |
| TW201604196A (zh) | 2011-02-02 | 2016-02-01 | 維泰克斯製藥公司 | 作為離子通道調節劑之吡咯并吡-螺環哌啶醯胺 |
| US10385070B2 (en) | 2011-02-18 | 2019-08-20 | Vertex Pharmaceuticals Incorporated | Chroman-spirocyclic piperidine amides as modulators of ion channels |
| CN104136442B (zh) * | 2012-01-16 | 2016-12-21 | 沃泰克斯药物股份有限公司 | 作为离子通道调节剂的吡喃‑螺环哌啶酰胺类 |
| KR102226587B1 (ko) | 2013-01-31 | 2021-03-11 | 버텍스 파마슈티칼스 인코포레이티드 | 나트륨 채널의 조절제로서의 퀴놀린 및 퀴나졸린 아미드 |
| PL2953931T3 (pl) | 2013-01-31 | 2017-09-29 | Vertex Pharmaceuticals Incorporated | Pirydonoamidy jako modulatory kanałów sodowych |
| RU2680401C2 (ru) | 2013-07-19 | 2019-02-21 | Вертекс Фармасьютикалз Инкорпорейтед | Сульфонамиды в качестве модуляторов натриевых каналов |
| RS59911B1 (sr) | 2013-10-14 | 2020-03-31 | Eisai R&D Man Co Ltd | Selektivno supstituisana jedinjenja hinolina |
| CA2920791C (en) | 2013-10-14 | 2021-11-16 | Eisai R&D Management Co., Ltd. | Selectively substituted quinoline compounds |
| SMT201800521T1 (it) | 2013-12-13 | 2018-11-09 | Vertex Pharma | Profarmaci di piridonammidi utili come modulatori di canali del sodio |
| TW201615643A (zh) * | 2014-06-02 | 2016-05-01 | 伊史帝夫博士實驗室股份有限公司 | 具有多重模式抗疼痛活性之1-氧雜-4,9-二氮雜螺十一烷化合物之烷基與芳基衍生物 |
| TW201615642A (zh) * | 2014-06-02 | 2016-05-01 | 伊史帝夫博士實驗室股份有限公司 | 具有多重模式抗疼痛活性的1-氧雜-4,9-二氮雜螺十一烷化合物之醯胺衍生物 |
| TWI685497B (zh) * | 2014-06-02 | 2020-02-21 | 西班牙商伊史帝夫製藥公司 | 具有多重模式抗疼痛活性的1-氧雜-4,9-二氮雜螺十一烷化合物之烷基衍生物 |
| PE20180694A1 (es) | 2015-07-31 | 2018-04-23 | Pfizer | Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-il-carbamato y derivados de 1,1,1-trifluoro-4-hidroxibutan-2-il-carbamato como inhibidores de magl |
| SI3365346T1 (sl) * | 2015-10-23 | 2020-04-30 | Esteve Pharmaceuticals, S.A. | Spojine oksa diazaspiro s protibolečinskim delovanjem |
| TW201734009A (zh) * | 2015-10-23 | 2017-10-01 | 艾斯提夫博士實驗股份有限公司 | 具有抗疼痛活性的經取代的□啉衍生物 |
| AR106444A1 (es) * | 2015-10-23 | 2018-01-17 | Esteve Labor Dr | Compuestos oxaazaespíricos con actividad contra el dolor |
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| CA2829803A1 (en) | 2012-09-20 |
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| CN103517910A (zh) | 2014-01-15 |
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| EP2686325B1 (en) | 2016-12-14 |
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| JP2014508169A (ja) | 2014-04-03 |
| AU2012229187A1 (en) | 2013-09-19 |
| WO2012125613A1 (en) | 2012-09-20 |
| NZ615014A (en) | 2016-08-26 |
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