JP5271917B2 - スピロクロマノン誘導体 - Google Patents
スピロクロマノン誘導体 Download PDFInfo
- Publication number
- JP5271917B2 JP5271917B2 JP2009545580A JP2009545580A JP5271917B2 JP 5271917 B2 JP5271917 B2 JP 5271917B2 JP 2009545580 A JP2009545580 A JP 2009545580A JP 2009545580 A JP2009545580 A JP 2009545580A JP 5271917 B2 JP5271917 B2 JP 5271917B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- chroman
- methyl
- carbonyl
- spiro
- 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.)
- Expired - Fee Related
Links
- 0 *C(CC1)=CC2=C1OC(CC1)(CC*1C(*N)=O)CC2=O Chemical compound *C(CC1)=CC2=C1OC(CC1)(CC*1C(*N)=O)CC2=O 0.000 description 1
- YJAWVMSEOSUZJL-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(C1)Oc(ccc(-c2cc(C(OC)=O)ccc2)c2)c2C1=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(C1)Oc(ccc(-c2cc(C(OC)=O)ccc2)c2)c2C1=O)=O YJAWVMSEOSUZJL-UHFFFAOYSA-N 0.000 description 1
- DVUHUNRRTXKZHI-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(C1)Oc(ccc(NC(OC)=O)c2)c2C1=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(C1)Oc(ccc(NC(OC)=O)c2)c2C1=O)=O DVUHUNRRTXKZHI-UHFFFAOYSA-N 0.000 description 1
- UEIKZERXUNEYOT-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(CC1O)Oc(cc2)c1cc2C#N)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(CC1O)Oc(cc2)c1cc2C#N)=O UEIKZERXUNEYOT-UHFFFAOYSA-N 0.000 description 1
- IVOYYNDEARJZBQ-UHFFFAOYSA-N CC(C)c(nc1)cc2c1OC(CC1)(CCN1C(c1cc(-c3n[nH]c[n]3)cc(-c3ccccc3)c1)=O)CC2=O Chemical compound CC(C)c(nc1)cc2c1OC(CC1)(CCN1C(c1cc(-c3n[nH]c[n]3)cc(-c3ccccc3)c1)=O)CC2=O IVOYYNDEARJZBQ-UHFFFAOYSA-N 0.000 description 1
- ZJOKPQULNBCMBI-VFKLRXJHSA-N CCOc(cc(cc1)C(O)=O)c1/C(/C=N)=C/NC Chemical compound CCOc(cc(cc1)C(O)=O)c1/C(/C=N)=C/NC ZJOKPQULNBCMBI-VFKLRXJHSA-N 0.000 description 1
- ZQMWQBSKKWRYLE-YFOFRGDXSA-N CCOc(cc(cc1)C(OC)=O)c1/C(/C=N)=C/NC Chemical compound CCOc(cc(cc1)C(OC)=O)c1/C(/C=N)=C/NC ZQMWQBSKKWRYLE-YFOFRGDXSA-N 0.000 description 1
- LEWFQNFGAKCHOQ-UHFFFAOYSA-N CCOc1cc(C(N(CC2)CCC2(C2)Oc(ccc(-c3cc(C(O)=O)cnc3)c3)c3C2=O)=O)cc(OCC)c1-c1c[n](C(F)F)nc1 Chemical compound CCOc1cc(C(N(CC2)CCC2(C2)Oc(ccc(-c3cc(C(O)=O)cnc3)c3)c3C2=O)=O)cc(OCC)c1-c1c[n](C(F)F)nc1 LEWFQNFGAKCHOQ-UHFFFAOYSA-N 0.000 description 1
- HXCPNMUCZFKWQB-UHFFFAOYSA-N COC(c1cc(-c2ccccc2)nc(C#N)c1)=O Chemical compound COC(c1cc(-c2ccccc2)nc(C#N)c1)=O HXCPNMUCZFKWQB-UHFFFAOYSA-N 0.000 description 1
- OSAZVOJFTYXFQG-UHFFFAOYSA-N COC(c1cc(OC)c(-c2ccccc2)c(OC)c1)=O Chemical compound COC(c1cc(OC)c(-c2ccccc2)c(OC)c1)=O OSAZVOJFTYXFQG-UHFFFAOYSA-N 0.000 description 1
- HQQHLUAKUORIMQ-UHFFFAOYSA-N COC(c1cc(OCc2ccccc2)nc(Cl)c1)=O Chemical compound COC(c1cc(OCc2ccccc2)nc(Cl)c1)=O HQQHLUAKUORIMQ-UHFFFAOYSA-N 0.000 description 1
- DRYKFTBVCITZCC-UHFFFAOYSA-N COC(c1cccc(-c(cc2)cc3c2OC2(CCNCC2)CC3=O)c1)=O Chemical compound COC(c1cccc(-c(cc2)cc3c2OC2(CCNCC2)CC3=O)c1)=O DRYKFTBVCITZCC-UHFFFAOYSA-N 0.000 description 1
- XVTOWXMESZWGLM-UHFFFAOYSA-N COc1cc(-c(cc2)cc3c2[nH]cc3)cc(C(N(CC2)CCC2(C2)Oc(ccc(-c3nnn[nH]3)c3)c3C2=O)=O)c1 Chemical compound COc1cc(-c(cc2)cc3c2[nH]cc3)cc(C(N(CC2)CCC2(C2)Oc(ccc(-c3nnn[nH]3)c3)c3C2=O)=O)c1 XVTOWXMESZWGLM-UHFFFAOYSA-N 0.000 description 1
- JMSPKCZEAWDVIB-UHFFFAOYSA-N Cc(c1c2ccc(Br)c1)n[n]2-c1ccccc1 Chemical compound Cc(c1c2ccc(Br)c1)n[n]2-c1ccccc1 JMSPKCZEAWDVIB-UHFFFAOYSA-N 0.000 description 1
- NGQPHMJPNAKEBV-UHFFFAOYSA-N N/C(/c(cc12)ccc1OC1(CCNCC1)CC2=O)=N\N Chemical compound N/C(/c(cc12)ccc1OC1(CCNCC1)CC2=O)=N\N NGQPHMJPNAKEBV-UHFFFAOYSA-N 0.000 description 1
- WMMHYTUQJAXSOU-UHFFFAOYSA-N NC(c1cccc(-c(cc2)cc3c2OC2(CCNCC2)CC3=O)c1)=O Chemical compound NC(c1cccc(-c(cc2)cc3c2OC2(CCNCC2)CC3=O)c1)=O WMMHYTUQJAXSOU-UHFFFAOYSA-N 0.000 description 1
- IFXITJNHMMBWBA-UHFFFAOYSA-N NNC(c1cc(C(O)=O)cc(N2CCCC2)c1)=N Chemical compound NNC(c1cc(C(O)=O)cc(N2CCCC2)c1)=N IFXITJNHMMBWBA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A—HUMAN NECESSITIES
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Child & Adolescent Psychology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Hospice & Palliative Care (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88030307P | 2007-01-12 | 2007-01-12 | |
| US60/880,303 | 2007-01-12 | ||
| PCT/US2008/000247 WO2008088692A2 (en) | 2007-01-12 | 2008-01-08 | Spirochromanon derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010515734A JP2010515734A (ja) | 2010-05-13 |
| JP2010515734A5 JP2010515734A5 (enExample) | 2011-02-10 |
| JP5271917B2 true JP5271917B2 (ja) | 2013-08-21 |
Family
ID=39636552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009545580A Expired - Fee Related JP5271917B2 (ja) | 2007-01-12 | 2008-01-08 | スピロクロマノン誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8138197B2 (enExample) |
| EP (1) | EP2120569B1 (enExample) |
| JP (1) | JP5271917B2 (enExample) |
| AU (1) | AU2008205642B2 (enExample) |
| CA (1) | CA2674530C (enExample) |
| WO (1) | WO2008088692A2 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE509023T1 (de) * | 2005-07-19 | 2011-05-15 | Merck Sharp & Dohme | Spirochromanon-derivate als acetyl-koenzym-a- carboxylase-hemmer |
| PE20081559A1 (es) * | 2007-01-12 | 2008-11-20 | Merck & Co Inc | DERIVADOS DE ESPIROCROMANONA SUSTITUIDOS COMO INHIBIDORES DE ACETIL CoA CARBOXILASA |
| EP2307422B1 (en) | 2008-07-04 | 2014-03-26 | Msd K.K. | Novel spirochromanone carboxylic acids |
| EP2310015A4 (en) | 2008-07-14 | 2011-10-26 | Cropsolution Inc | ACETYL-COENZYME-CARBOXYLASE MODULATORS AND METHODS OF USE THEREOF |
| US20110190365A1 (en) * | 2008-08-14 | 2011-08-04 | Bayer Crop Science Ag | Insecticidal 4-phenyl-1H-pyrazoles |
| US8653098B2 (en) | 2008-11-20 | 2014-02-18 | Genentech, Inc. | Pyrazolopyridine PI3K inhibitor compounds and methods of use |
| EP2308866A1 (de) | 2009-10-09 | 2011-04-13 | Bayer CropScience AG | Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide |
| PH12012500778A1 (en) | 2009-10-30 | 2012-11-26 | Janssen Pharmaceutica Nv | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
| WO2011076725A1 (en) | 2009-12-21 | 2011-06-30 | Bayer Cropscience Ag | Thienylpyri (mi) dinylazole and their use for controlling phytopathogenic fungi |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| US8598164B2 (en) | 2010-05-06 | 2013-12-03 | Vertex Pharmaceuticals Incorporated | Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| DK2621493T3 (en) * | 2010-09-30 | 2016-10-24 | Pfizer | N1 PYRAZOLOSPIROKETON-ACETYL-CoA carboxylase INHIBITORS |
| JP2013542960A (ja) * | 2010-11-08 | 2013-11-28 | グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー2、リミテッド | 脂肪酸シンターゼ阻害剤 |
| KR101923367B1 (ko) | 2011-02-02 | 2018-12-04 | 버텍스 파마슈티칼스 인코포레이티드 | 이온 채널의 조절제로서의 피롤로피라진―스피로사이클릭 피페리딘 아미드 |
| WO2012112743A1 (en) | 2011-02-18 | 2012-08-23 | Vertex Pharmaceuticals Incorporated | Chroman - spirocyclic piperidine amides as modulators of ion channels |
| US8828996B2 (en) | 2011-03-14 | 2014-09-09 | Vertex Pharmaceuticals Incorporated | Morpholine-spirocyclic piperidine amides as modulators of ion channels |
| TW201300393A (zh) * | 2011-05-20 | 2013-01-01 | Kowa Co | 新穎之螺哌啶衍生物及含有其之醫藥 |
| JP6115962B2 (ja) | 2011-06-27 | 2017-04-19 | ヤンセン ファーマシューティカ エヌ.ベー. | 1−アリール−4−メチル−[1,2,4]トリアゾロ[4,3−a]キノキサリン誘導体 |
| CA2873439A1 (en) * | 2012-05-22 | 2013-11-28 | Actelion Pharmaceuticals Ltd | New process for the preparation of 2-cyclopentyl-6-methoxy-isonicotinic acid |
| WO2014001314A1 (en) | 2012-06-26 | 2014-01-03 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| AU2013289284B2 (en) | 2012-07-09 | 2017-03-30 | Janssen Pharmaceutica Nv | Inhibitors of phosphodiesterase 10 enzyme |
| WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
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| ATE509023T1 (de) * | 2005-07-19 | 2011-05-15 | Merck Sharp & Dohme | Spirochromanon-derivate als acetyl-koenzym-a- carboxylase-hemmer |
| WO2008065508A1 (en) * | 2006-11-29 | 2008-06-05 | Pfizer Products Inc. | Spiroketone acetyl-coa carboxylase inhibitors |
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| EP2123652A1 (en) * | 2007-02-20 | 2009-11-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
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- 2008-01-08 JP JP2009545580A patent/JP5271917B2/ja not_active Expired - Fee Related
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- 2008-01-08 EP EP08705516.6A patent/EP2120569B1/en not_active Not-in-force
- 2008-01-08 AU AU2008205642A patent/AU2008205642B2/en not_active Ceased
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| WO2008088692A3 (en) | 2008-09-18 |
| JP2010515734A (ja) | 2010-05-13 |
| EP2120569A2 (en) | 2009-11-25 |
| WO2008088692A2 (en) | 2008-07-24 |
| US20090270436A1 (en) | 2009-10-29 |
| CA2674530A1 (en) | 2008-07-24 |
| CA2674530C (en) | 2014-09-16 |
| EP2120569A4 (en) | 2010-12-08 |
| AU2008205642B2 (en) | 2013-06-06 |
| EP2120569B1 (en) | 2013-08-14 |
| AU2008205642A1 (en) | 2008-07-24 |
| US8138197B2 (en) | 2012-03-20 |
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