KR20130009577A - 야누스 키나아제 3의 피페리딘 억제제 - Google Patents
야누스 키나아제 3의 피페리딘 억제제 Download PDFInfo
- Publication number
- KR20130009577A KR20130009577A KR1020117026990A KR20117026990A KR20130009577A KR 20130009577 A KR20130009577 A KR 20130009577A KR 1020117026990 A KR1020117026990 A KR 1020117026990A KR 20117026990 A KR20117026990 A KR 20117026990A KR 20130009577 A KR20130009577 A KR 20130009577A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- deuterium
- formula
- methyl
- group
- 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.)
- Ceased
Links
- 0 CC(*)(*)[C@](**)(C(*)*(*)N(C1(*)*)C(C(*)(C#N)I)=O)[C@@]1(*)N(C(*)(*)*)c1c(c(*)c(*)[n]2*)c2nc(*)n1 Chemical compound CC(*)(*)[C@](**)(C(*)*(*)N(C1(*)*)C(C(*)(C#N)I)=O)[C@@]1(*)N(C(*)(*)*)c1c(c(*)c(*)[n]2*)c2nc(*)n1 0.000 description 39
- ZJCSSAVUFFCYCC-UHFFFAOYSA-N CCOC(C(CC(N(Cc1ccccc1)C1)=O)=C1O)=O Chemical compound CCOC(C(CC(N(Cc1ccccc1)C1)=O)=C1O)=O ZJCSSAVUFFCYCC-UHFFFAOYSA-N 0.000 description 1
- IXZFDJXHLQQSGQ-UHFFFAOYSA-N CCOC(CCC(Cl)=O)=O Chemical compound CCOC(CCC(Cl)=O)=O IXZFDJXHLQQSGQ-UHFFFAOYSA-N 0.000 description 1
- GIOPHLGQJCNFBA-UHFFFAOYSA-N CCOC(CCC(N(CC(OCC)=O)Cc1ccccc1)=O)=O Chemical compound CCOC(CCC(N(CC(OCC)=O)Cc1ccccc1)=O)=O GIOPHLGQJCNFBA-UHFFFAOYSA-N 0.000 description 1
- ULOLIZHBYWAICY-UHFFFAOYSA-N CCOC(CNCc1ccccc1)=O Chemical compound CCOC(CNCc1ccccc1)=O ULOLIZHBYWAICY-UHFFFAOYSA-N 0.000 description 1
- ZPLBIDRVDMCSNE-UHFFFAOYSA-N OC(CN(Cc1ccccc1)C(C1)=O)=C1C(OCc1ccccc1)=O Chemical compound OC(CN(Cc1ccccc1)C(C1)=O)=C1C(OCc1ccccc1)=O ZPLBIDRVDMCSNE-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N OCc1ccccc1 Chemical compound OCc1ccccc1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/04—Artificial tears; Irrigation solutions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17085809P | 2009-04-20 | 2009-04-20 | |
| US61/170,858 | 2009-04-20 | ||
| US30088710P | 2010-02-03 | 2010-02-03 | |
| US61/300,887 | 2010-02-03 | ||
| PCT/US2010/031773 WO2010123919A2 (en) | 2009-04-20 | 2010-04-20 | Piperidine inhibitors of janus kinase 3 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20130009577A true KR20130009577A (ko) | 2013-01-23 |
Family
ID=43011721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020117026990A Ceased KR20130009577A (ko) | 2009-04-20 | 2010-04-20 | 야누스 키나아제 3의 피페리딘 억제제 |
Country Status (10)
| Country | Link |
|---|---|
| US (4) | US8299084B2 (enExample) |
| EP (2) | EP2421867B1 (enExample) |
| JP (3) | JP5709276B2 (enExample) |
| KR (1) | KR20130009577A (enExample) |
| CN (2) | CN102459270B (enExample) |
| AU (2) | AU2010239396B2 (enExample) |
| BR (1) | BRPI1007737A2 (enExample) |
| CA (2) | CA3025627C (enExample) |
| ES (1) | ES2552805T3 (enExample) |
| WO (1) | WO2010123919A2 (enExample) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102459270B (zh) | 2009-04-20 | 2015-04-29 | 奥斯拜客斯制药有限公司 | Janus激酶3的哌啶抑制剂 |
| EP2481411A1 (en) * | 2011-01-27 | 2012-08-01 | Ratiopharm GmbH | Oral dosage forms for modified release comprising the JAK3 inhibitor tasocitinib |
| US20120195966A1 (en) * | 2011-01-27 | 2012-08-02 | Frank Sievert | Oral dosage form for modified release comprising a jak3 inhibitor |
| EP2675275B1 (en) | 2011-02-14 | 2017-12-20 | The Regents Of The University Of Michigan | Compositions and methods for the treatment of obesity and related disorders |
| US20150291594A1 (en) * | 2012-08-14 | 2015-10-15 | Concert Pharmaceuticals, Inc. | Deuterated Ponatinib |
| CN102875555A (zh) * | 2012-09-27 | 2013-01-16 | 同济大学 | 一种JAK抑制剂Tofacitinib的合成方法 |
| US9481679B2 (en) * | 2012-12-17 | 2016-11-01 | Sun Pharmaceutical Industries Limited | Process for the preparation of tofacitinib and intermediates thereof |
| US9757395B2 (en) | 2012-12-20 | 2017-09-12 | Otitopic Inc. | Dry powder inhaler and methods of use |
| US9757529B2 (en) | 2012-12-20 | 2017-09-12 | Otitopic Inc. | Dry powder inhaler and methods of use |
| WO2014102826A1 (en) * | 2012-12-28 | 2014-07-03 | Glenmark Pharmaceuticals Limited; | The present invention relates to process for the preparation of tofacitinib and intermediates thereof. |
| EP2943489B1 (en) | 2013-01-09 | 2018-04-11 | Concert Pharmaceuticals Inc. | Deuterated momelotinib |
| LT2945939T (lt) | 2013-01-15 | 2020-07-27 | Incyte Holdings Corporation | Triazolkarboksamidai ir piridinkarboksamido junginiai, naudotini kaip pim kinazės inhibitoriai |
| CN103965114B (zh) * | 2013-01-28 | 2016-01-06 | 苏州泽璟生物制药有限公司 | 氘代的苯基氨基嘧啶化合物以及包含该化合物的药物组合物 |
| CN103073552B (zh) * | 2013-02-05 | 2015-08-12 | 华润赛科药业有限责任公司 | 一种无定型枸橼酸托法替尼的制备方法 |
| JP6041823B2 (ja) | 2013-03-16 | 2016-12-14 | ファイザー・インク | トファシチニブの経口持続放出剤形 |
| US10149823B2 (en) | 2013-04-30 | 2018-12-11 | Otitopic Inc. | Dry powder formulations and methods of use |
| WO2014179734A1 (en) | 2013-05-02 | 2014-11-06 | The Regents Of The University Of Michigan | Deuterated amlexanox |
| WO2014195978A2 (en) * | 2013-06-05 | 2014-12-11 | Msn Laboratories Limited | PROCESS FOR THE PREPARATION OF (3R,4R)-4-METHYL-3-(METHYL-7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL-AMINO)-ß-OXO-1-PIPERIDINEPROPANENITRILE AND ITS SALTS |
| CN104447751A (zh) * | 2013-09-16 | 2015-03-25 | 天津市汉康医药生物技术有限公司 | 一种托法替尼化合物 |
| CN104447752A (zh) * | 2013-09-16 | 2015-03-25 | 天津市汉康医药生物技术有限公司 | 一种托法替尼水合物及其制备方法 |
| CN104292231B (zh) * | 2013-09-17 | 2016-11-30 | 广东东阳光药业有限公司 | 一种枸橼酸托法替尼的制备方法 |
| CN104513248B (zh) * | 2013-09-30 | 2019-05-24 | 重庆医药工业研究院有限责任公司 | 一种托法替尼中间体的纯化方法 |
| CN105873931B (zh) * | 2013-10-08 | 2018-10-16 | 广东东阳光药业有限公司 | 托法替布柠檬酸盐 |
| CN103819474A (zh) * | 2013-11-04 | 2014-05-28 | 湖南华腾制药有限公司 | 一种托法替尼的制备方法 |
| BR112015025543B1 (pt) | 2013-12-09 | 2020-11-03 | Unichem Laboratories Limited | processo para a preparação de (3r,4r)-(1-benzil-4- metilpiperidina-3-il)-metilamina e compostos intermediários |
| EA201691582A1 (ru) | 2014-02-07 | 2017-01-30 | Оспекс Фармасьютикалз, Инк. | Новые фармацевтические препараты |
| US20150284327A1 (en) * | 2014-04-04 | 2015-10-08 | Auspex Pharmaceuticals, Inc. | Oxindole inhibitors of tyrosine kinase |
| CN104710346B (zh) * | 2015-02-15 | 2017-04-12 | 江苏苏利精细化工股份有限公司 | 一种合成顺式‑1‑苄基‑3‑甲氨基‑4‑甲基‑哌啶的方法 |
| EP3078665A1 (en) * | 2015-04-10 | 2016-10-12 | OLON S.p.A. | Efficient method for the preparation of tofacitinib citrate |
| WO2016192563A1 (zh) * | 2015-05-29 | 2016-12-08 | 南京明德新药研发股份有限公司 | Janus激酶抑制剂 |
| AR105967A1 (es) | 2015-09-09 | 2017-11-29 | Incyte Corp | Sales de un inhibidor de pim quinasa |
| WO2017059251A1 (en) | 2015-10-02 | 2017-04-06 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
| CN105440039A (zh) * | 2015-11-24 | 2016-03-30 | 山东淄博新达制药有限公司 | 枸橼酸托法替布的合成方法 |
| EP3407974A4 (en) | 2016-01-29 | 2019-08-28 | The Regents Of The University Of Michigan | Amlexanox Analogs |
| CN105884781B (zh) * | 2016-04-18 | 2018-04-20 | 山东罗欣药业集团股份有限公司 | 一种枸橼酸托法替布的制备方法 |
| CN106188064A (zh) * | 2016-07-07 | 2016-12-07 | 国药集团容生制药有限公司 | 一种N‑甲基‑N‑((3R,4R)‑4‑甲基吡啶‑3‑基)‑7H‑吡咯并[2,3‑d]嘧啶‑4‑胺的制备方法 |
| CN105949204A (zh) * | 2016-07-25 | 2016-09-21 | 国药集团容生制药有限公司 | 一种N-((3R,4R)-1-苄基-4-甲基吡啶-3-基)-N-甲基-7H-吡咯并[2,3-d]嘧啶-4-胺的制备方法 |
| EP3421455B1 (en) * | 2017-06-29 | 2019-03-27 | F.I.S.- Fabbrica Italiana Sintetici S.p.A. | Improved process for the preparation of chiral 3-amino-piperidins, useful intermediates for the preparation of tofacitinib |
| CN109293682A (zh) * | 2017-07-25 | 2019-02-01 | 重庆医药工业研究院有限责任公司 | 一种托法替布杂质及其制备方法 |
| US10786456B2 (en) | 2017-09-22 | 2020-09-29 | Otitopic Inc. | Inhaled aspirin and magnesium to treat inflammation |
| CN115919780A (zh) | 2017-09-22 | 2023-04-07 | 维克图拉公司 | 含有硬脂酸镁的干粉组合物 |
| CN108358930A (zh) * | 2018-02-05 | 2018-08-03 | 南京法恩化学有限公司 | 一种枸橼酸托法替尼的制备方法 |
| CN109776547A (zh) * | 2019-03-22 | 2019-05-21 | 北京新领先医药科技发展有限公司 | 一种枸橼酸托法替布的制备方法 |
| EP4153565A1 (en) * | 2020-05-20 | 2023-03-29 | F. Hoffmann-La Roche AG | Benzylpyridinium reagent for mass spectrometry |
| CN111848496B (zh) * | 2020-07-28 | 2021-10-08 | 湖南华纳大药厂手性药物有限公司 | 一种托法替布中间体胺及其双盐酸盐的制备方法 |
| CN112679508B (zh) * | 2021-03-09 | 2021-08-10 | 正大天晴药业集团南京顺欣制药有限公司 | 一种托法替布中间体的制备方法 |
| WO2023248010A2 (en) | 2022-06-23 | 2023-12-28 | Synovo Gmbh | Targeted modulators of jak3 for treatment of inflammatory and autoimmune diseases |
| US20250102479A1 (en) * | 2023-09-22 | 2025-03-27 | Thermo Finnigan Llc | Method of utilizing deuterium gas for chromatography applications, deuterium gas generator and devices for conservation thereof |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3696884B2 (ja) | 1994-03-25 | 2005-09-21 | アイソテクニカ、インコーポレーテッド | ジュウテリウム化による薬物の効能の増強 |
| US6221335B1 (en) * | 1994-03-25 | 2001-04-24 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| CA2198382A1 (en) * | 1994-09-30 | 1996-04-11 | Novartis Ag | 1-acyl-4-aliphatylaminopiperidine compounds |
| PA8474101A1 (es) * | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | Compuestos de pirrolo [2,3-d] pirimidina |
| RS50087B (sr) * | 1998-06-19 | 2009-01-22 | Pfizer Products Inc., | Pirolo (2,3-d) pirimidin jedinjenja |
| US6440710B1 (en) * | 1998-12-10 | 2002-08-27 | The Scripps Research Institute | Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds |
| EP1104760B1 (en) * | 1999-12-03 | 2003-03-12 | Pfizer Products Inc. | Sulfamoylheteroaryl pyrazole compounds as anti-inflammatory/analgesic agents |
| CZ303875B6 (cs) * | 1999-12-10 | 2013-06-05 | Pfizer Products Inc. | Pyrrolo[2,3-d]pyrimidinová sloucenina a farmaceutická kompozice s jejím obsahem |
| EP1134290A3 (en) * | 2000-03-14 | 2004-01-02 | Pfizer Products Inc. | Pharmacophore models for the identification of the CYP2D6 inhibitory potency of selective serotonin reuptake inhibitors |
| EA006153B1 (ru) * | 2000-06-26 | 2005-10-27 | Пфайзер Продактс Инк. | СОЕДИНЕНИЯ ПИРРОЛО[2,3-d]ПИРИМИДИНА В КАЧЕСТВЕ ИММУНОДЕПРЕССАНТОВ |
| US7301023B2 (en) * | 2001-05-31 | 2007-11-27 | Pfizer Inc. | Chiral salt resolution |
| GT200200234A (es) * | 2001-12-06 | 2003-06-27 | Compuestos cristalinos novedosos | |
| TW200413273A (en) * | 2002-11-15 | 2004-08-01 | Wako Pure Chem Ind Ltd | Heavy hydrogenation method of heterocyclic rings |
| EP1572649A2 (en) * | 2002-11-21 | 2005-09-14 | Pfizer Products Inc. | 3-amino-piperidine derivatives and processes for their preparation |
| CA2507392A1 (en) | 2002-11-26 | 2004-06-10 | Pfizer Products Inc. | Method of treatment of transplant rejection |
| WO2005051393A1 (en) | 2003-11-25 | 2005-06-09 | Pfizer Products Inc. | Method of treatment of atherosclerosis |
| MXPA06007002A (es) | 2003-12-17 | 2006-08-31 | Pfizer Prod Inc | Compuestos de pirrolo[2,3-d]pirimidina para tratar rechazo de transplantes. |
| WO2005063251A1 (en) | 2003-12-17 | 2005-07-14 | Pfizer Products Inc. | Modified stent useful for delivery of drugs along stent strut |
| US20050137679A1 (en) * | 2003-12-17 | 2005-06-23 | Pfizer Inc | Modified stent useful for delivery of drugs along stent strut |
| WO2005063318A1 (en) | 2003-12-17 | 2005-07-14 | Pfizer Products Inc. | Stent with therapeutically active drug coated thereon |
| EP1755680A1 (en) | 2004-05-03 | 2007-02-28 | Novartis AG | Combinations comprising a s1p receptor agonist and a jak3 kinase inhibitor |
| WO2006013114A1 (en) | 2004-08-06 | 2006-02-09 | Develogen Aktiengesellschaft | Use of a timp-2 secreted protein product for preventing and treating pancreatic diseases and/or obesity and/or metabolic syndrome |
| KR20070085433A (ko) | 2004-11-24 | 2007-08-27 | 노파르티스 아게 | Jak 저해제들과 bcr-abl, flt-3, fak 또는raf 키나제 저해제들 중 하나 이상의 조합물 |
| ATE542535T1 (de) | 2005-05-04 | 2012-02-15 | Develogen Ag | Verwendung von azapaullonen zur vorbeugung und behandlung pankreatischer autoimmunkrankheiten |
| WO2006117212A2 (en) | 2005-05-04 | 2006-11-09 | Develogen Aktiengesellschaft | Use of gsk-3 inhibitors for preventing and treating pancreatic autoimmune disorders |
| WO2006136374A2 (en) | 2005-06-20 | 2006-12-28 | Develogen Aktiengesellschaft | Use of gip and/or vitamin d3 analogues thereof for enhancing stem or progenitor cell differentiation into insulin producing cells |
| US20080033011A1 (en) * | 2005-07-29 | 2008-02-07 | Concert Pharmaceuticals Inc. | Novel benzo[d][1,3]-dioxol derivatives |
| MX2008001334A (es) | 2005-07-29 | 2008-03-24 | Pfizer Prod Inc | Derivados de pirrolo [2,3-d]pirimidina, sus intermedios y sintesis. |
| US7750168B2 (en) * | 2006-02-10 | 2010-07-06 | Sigma-Aldrich Co. | Stabilized deuteroborane-tetrahydrofuran complex |
| GB0605691D0 (en) * | 2006-03-21 | 2006-05-03 | Novartis Ag | Organic Compounds |
| WO2008029237A2 (en) | 2006-09-05 | 2008-03-13 | Pfizer Products Inc. | Combination therapies for rheumatoid arthritis |
| US20090182035A1 (en) | 2007-04-11 | 2009-07-16 | Alcon Research, Ltd. | Use of a combination of olopatadine and cilomilast to treat non-infectious rhinitis and allergic conjunctivitis |
| US20080254029A1 (en) * | 2007-04-11 | 2008-10-16 | Alcon Research, Ltd. | Use of an Inhibitor of TNFa Plus an Antihistamine to Treat Allergic Rhinitis and Allergic Conjunctivitis |
| EP2175858B1 (en) | 2007-07-11 | 2014-09-10 | Pfizer Inc. | Pharmaceutical compositions and methods of treating dry eye disorders |
| JP5492194B2 (ja) | 2008-05-13 | 2014-05-14 | アイアールエム・リミテッド・ライアビリティ・カンパニー | キナーゼ阻害剤としての縮合窒素含有ヘテロ環およびその組成物 |
| HUE028347T2 (en) | 2008-06-10 | 2016-12-28 | Abbvie Inc | Tricyclic compounds |
| CN102459270B (zh) | 2009-04-20 | 2015-04-29 | 奥斯拜客斯制药有限公司 | Janus激酶3的哌啶抑制剂 |
-
2010
- 2010-04-20 CN CN201080025178.1A patent/CN102459270B/zh active Active
- 2010-04-20 CN CN201510171918.7A patent/CN104817561B/zh active Active
- 2010-04-20 EP EP10767652.0A patent/EP2421867B1/en active Active
- 2010-04-20 WO PCT/US2010/031773 patent/WO2010123919A2/en not_active Ceased
- 2010-04-20 CA CA3025627A patent/CA3025627C/en active Active
- 2010-04-20 EP EP15002523.7A patent/EP3026052A1/en not_active Withdrawn
- 2010-04-20 AU AU2010239396A patent/AU2010239396B2/en active Active
- 2010-04-20 BR BRPI1007737-5A patent/BRPI1007737A2/pt not_active IP Right Cessation
- 2010-04-20 ES ES10767652.0T patent/ES2552805T3/es active Active
- 2010-04-20 KR KR1020117026990A patent/KR20130009577A/ko not_active Ceased
- 2010-04-20 US US12/763,858 patent/US8299084B2/en active Active
- 2010-04-20 JP JP2012506006A patent/JP5709276B2/ja active Active
- 2010-04-20 CA CA2759026A patent/CA2759026C/en active Active
-
2012
- 2012-09-26 US US13/627,747 patent/US8962638B2/en active Active
-
2015
- 2015-01-14 US US14/596,784 patent/US9493469B2/en active Active
- 2015-02-26 JP JP2015037398A patent/JP5932080B2/ja active Active
-
2016
- 2016-04-20 JP JP2016084849A patent/JP6145534B2/ja active Active
- 2016-07-18 AU AU2016206214A patent/AU2016206214B2/en active Active
- 2016-08-05 US US15/229,267 patent/US9856261B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6145534B2 (ja) | ヤヌスキナーゼ3のピペリジンインヒビター | |
| US9498481B2 (en) | Cyclopropyl modulators of P2Y12 receptor | |
| KR20110048571A (ko) | 면역 기능을 지닌 2―옥소―1,2―다이하이드로―퀴놀린 조절제 | |
| WO2010028254A2 (en) | Substituted quinazoline inhibitors of growth factor receptor tyrosine kinases | |
| KR20120120970A (ko) | 티로신 키나아제의 트리메톡시페닐 저해제 | |
| WO2010123999A2 (en) | 1-methylpyrazole modulators of substance p, calcitonin gene-related peptide, adrenergic receptor, and/or 5-ht receptor | |
| US20100152283A1 (en) | Tetrahydrocannabinol modulators of cannabinoid receptors | |
| HK1238626A1 (en) | Preparation of deuterated piperidine inhibitors of janus kinase 3 | |
| HK1228888A1 (en) | Deuterated derivatives of ticagrelor for medical use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20111111 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| AMND | Amendment | ||
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| AMND | Amendment | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20150303 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20160719 Patent event code: PE09021S01D |
|
| AMND | Amendment | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20170228 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20160719 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |
|
| AMND | Amendment | ||
| PX0901 | Re-examination |
Patent event code: PX09011S01I Patent event date: 20170228 Comment text: Decision to Refuse Application Patent event code: PX09012R01I Patent event date: 20161019 Comment text: Amendment to Specification, etc. Patent event code: PX09012R01I Patent event date: 20150303 Comment text: Amendment to Specification, etc. Patent event code: PX09012R01I Patent event date: 20111202 Comment text: Amendment to Specification, etc. |
|
| PX0601 | Decision of rejection after re-examination |
Comment text: Decision to Refuse Application Patent event code: PX06014S01D Patent event date: 20170707 Comment text: Amendment to Specification, etc. Patent event code: PX06012R01I Patent event date: 20170531 Comment text: Decision to Refuse Application Patent event code: PX06011S01I Patent event date: 20170228 Comment text: Amendment to Specification, etc. Patent event code: PX06012R01I Patent event date: 20161019 Comment text: Notification of reason for refusal Patent event code: PX06013S01I Patent event date: 20160719 Comment text: Amendment to Specification, etc. Patent event code: PX06012R01I Patent event date: 20150303 Comment text: Amendment to Specification, etc. Patent event code: PX06012R01I Patent event date: 20111202 |