CN101610767A - 经取代的唑烷酮类化合物的组合疗法 - Google Patents
经取代的唑烷酮类化合物的组合疗法 Download PDFInfo
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- CN101610767A CN101610767A CNA2007800491463A CN200780049146A CN101610767A CN 101610767 A CN101610767 A CN 101610767A CN A2007800491463 A CNA2007800491463 A CN A2007800491463A CN 200780049146 A CN200780049146 A CN 200780049146A CN 101610767 A CN101610767 A CN 101610767A
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- Prior art keywords
- oxo
- methyl
- chloro
- phenyl
- oxazolidine
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- UXWQXBSQQHAGMG-UHFFFAOYSA-N tert-butyl n-[(4-aminophenyl)methyl]carbamate Chemical compound CC(C)(C)OC(=O)NCC1=CC=C(N)C=C1 UXWQXBSQQHAGMG-UHFFFAOYSA-N 0.000 description 1
- HHNRJXCRSBVTPW-UHFFFAOYSA-N tert-butyl n-[[4-[5-[[(5-chlorothiophene-2-carbonyl)amino]methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl]methyl]carbamate Chemical compound C1=CC(CNC(=O)OC(C)(C)C)=CC=C1N1C(=O)OC(CNC(=O)C=2SC(Cl)=CC=2)C1 HHNRJXCRSBVTPW-UHFFFAOYSA-N 0.000 description 1
- JHLVEBNWCCKSGY-UHFFFAOYSA-N tert-butyl n-methylcarbamate Chemical compound CNC(=O)OC(C)(C)C JHLVEBNWCCKSGY-UHFFFAOYSA-N 0.000 description 1
- VBUWHAJDOUIJMV-UHFFFAOYSA-N tert-butyl n-propylcarbamate Chemical compound CCCNC(=O)OC(C)(C)C VBUWHAJDOUIJMV-UHFFFAOYSA-N 0.000 description 1
- DQQJBEAXSOOCPG-UHFFFAOYSA-N tert-butyl n-pyrrolidin-3-ylcarbamate Chemical compound CC(C)(C)OC(=O)NC1CCNC1 DQQJBEAXSOOCPG-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical compound C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 description 1
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
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- VFJYIHQDILEQNR-UHFFFAOYSA-M trimethylsulfanium;iodide Chemical compound [I-].C[S+](C)C VFJYIHQDILEQNR-UHFFFAOYSA-M 0.000 description 1
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Abstract
Description
时间 | A:% | B:% | 流速 |
0.00 | 10.0 | 90.0 | 0.50 |
4.00 | 90.0 | 10.0 | 0.50 |
6.00 | 90.0 | 10.0 | 0.50 |
6.10 | 10.0 | 90.0 | 1.00 |
7.50 | 10.0 | 90.0 | 0.50 |
Claims (11)
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DE102006051625A DE102006051625A1 (de) | 2006-11-02 | 2006-11-02 | Kombinationstherapie substituierter Oxazolidinone |
DE102006051625.7 | 2006-11-02 | ||
PCT/EP2007/009068 WO2008052671A2 (de) | 2006-11-02 | 2007-10-19 | Kombinationstherapie substituierter oxazolidinone |
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CN101610767A true CN101610767A (zh) | 2009-12-23 |
CN101610767B CN101610767B (zh) | 2013-03-13 |
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EP (1) | EP2099453B1 (zh) |
JP (1) | JP5379012B2 (zh) |
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CN (1) | CN101610767B (zh) |
CA (1) | CA2668068C (zh) |
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DK (1) | DK2099453T3 (zh) |
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LT (2) | LT2099453T (zh) |
LU (1) | LUC00063I2 (zh) |
PL (1) | PL2099453T3 (zh) |
PT (1) | PT2099453T (zh) |
SI (1) | SI2099453T1 (zh) |
WO (1) | WO2008052671A2 (zh) |
Cited By (10)
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CN102746287A (zh) * | 2012-06-21 | 2012-10-24 | 成都苑东药业有限公司 | 一种恶唑烷酮化合物及其制备方法 |
CN102796091A (zh) * | 2011-05-24 | 2012-11-28 | 北大方正集团有限公司 | 取代的噁唑烷酮化合物及其制备方法和应用 |
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CN104402876A (zh) * | 2014-11-25 | 2015-03-11 | 沈阳药科大学 | 噁唑烷酮类化合物及其应用 |
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CN104478866A (zh) * | 2014-12-05 | 2015-04-01 | 广东东阳光药业有限公司 | 噁唑烷酮类化合物及其在药物中的应用 |
CN104497008A (zh) * | 2014-12-09 | 2015-04-08 | 广东东阳光药业有限公司 | 取代噁唑烷酮类化合物及其使用方法和用途 |
CN104557900A (zh) * | 2014-12-23 | 2015-04-29 | 中国药科大学 | 噁唑烷酮类化合物及其制备方法与医药用途 |
CN104693139A (zh) * | 2011-01-07 | 2015-06-10 | 浙江九洲药业股份有限公司 | 一种合成利伐沙班中间体的新工艺 |
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DE10355461A1 (de) | 2003-11-27 | 2005-06-23 | Bayer Healthcare Ag | Verfahren zur Herstellung einer festen, oral applizierbaren pharmazeutischen Zusammensetzung |
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DE102006051625A1 (de) | 2006-11-02 | 2008-05-08 | Bayer Materialscience Ag | Kombinationstherapie substituierter Oxazolidinone |
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EP3078378B1 (en) | 2015-04-08 | 2020-06-24 | Vaiomer | Use of factor xa inhibitors for regulating glycemia |
CA3060345A1 (en) | 2017-06-23 | 2018-12-27 | Chiesi Farmaceutici S.P.A. | Method of preventing of systemic-to-pulmonary-artery shunt thrombosis |
US10828310B2 (en) * | 2018-02-02 | 2020-11-10 | Bayer Pharma Aktiengesellschaft | Reducing the risk of cardiovascular events |
CN110172060A (zh) * | 2018-12-27 | 2019-08-27 | 苏州二叶制药有限公司 | 利伐沙班、合成及精制方法 |
US11608320B2 (en) | 2020-02-02 | 2023-03-21 | Kuwait University | Oxazolidinone hydroxamic acid derivatives |
Family Cites Families (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2811555A (en) * | 1955-05-02 | 1957-10-29 | Eastman Kodak Co | Reduction of 2-nitroso-5-diethylaminotoluene |
US3279880A (en) * | 1965-07-12 | 1966-10-18 | Eastman Kodak Co | Polyester textile material dyed with 1-hydroxy-4-n-p-(2'-pyrrolidonyl-1-) phenyl-amino anthraquinones |
LU80081A1 (fr) * | 1977-08-26 | 1979-05-15 | Delalande Sa | Nouvelles hydroxymethyl-5 oxazolidinones-2,leur procede de preparation et leur application therapeutique |
US4128654A (en) * | 1978-02-10 | 1978-12-05 | E. I. Du Pont De Nemours And Company | 5-Halomethyl-3-phenyl-2-oxazolidinones |
US4500519A (en) * | 1978-11-06 | 1985-02-19 | Choay S.A. | Mucopolysaccharides having biological properties, preparation and method of use |
US4327725A (en) * | 1980-11-25 | 1982-05-04 | Alza Corporation | Osmotic device with hydrogel driving member |
HU190072B (en) * | 1983-03-11 | 1986-08-28 | Biogal Gyogyszergyar,Hu | Process for production of medical preparatives with sinergetic influence |
US4765989A (en) * | 1983-05-11 | 1988-08-23 | Alza Corporation | Osmotic device for administering certain drugs |
DE3822650A1 (de) * | 1988-07-05 | 1990-02-01 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
US5254577A (en) * | 1988-07-29 | 1993-10-19 | The Du Pont Merck Pharmaceutical Company | Aminomethyloxooxazolidinyl arylbenzene derivatives useful as antibacterial agents |
US5654285A (en) * | 1991-04-06 | 1997-08-05 | Astra Pharmaceuticals Limited | ADP and ATP analogues, process for making and administration to inhibit ADP-induced platelet aggregation |
AU667198B2 (en) * | 1991-11-01 | 1996-03-14 | Pharmacia & Upjohn Company | Substituted aryl- and heteroarylphenyloxazolidinones useful as antibacterial agents |
US5349045A (en) * | 1993-01-26 | 1994-09-20 | United States Surgical Corporation | Polymer derived from cyclic amide and medical devices manufactured therefrom |
DK0623615T3 (da) * | 1993-05-01 | 1999-12-13 | Merck Patent Gmbh | Adhæsionsreceptor-antagonister |
US5688792A (en) * | 1994-08-16 | 1997-11-18 | Pharmacia & Upjohn Company | Substituted oxazine and thiazine oxazolidinone antimicrobials |
DE4332384A1 (de) * | 1993-09-23 | 1995-03-30 | Merck Patent Gmbh | Adhäsionsrezeptor-Antagonisten III |
RU2154645C2 (ru) * | 1995-02-03 | 2000-08-20 | Фармация Энд Апджон Компани | Фенилоксазолидиноны, замещенные в кольце гетероароматическими кольцами, в качестве антимикробных агентов |
HRP960159A2 (en) * | 1995-04-21 | 1997-08-31 | Bayer Ag | Benzocyclopentane oxazolidinones containing heteroatoms |
RU2158607C2 (ru) * | 1995-07-03 | 2000-11-10 | Санкио Компани Лимитед | Лечение артериосклероза и ксантомы |
DE19524765A1 (de) * | 1995-07-07 | 1997-01-09 | Boehringer Mannheim Gmbh | Neue Oxazolidinonderivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
DE19601264A1 (de) * | 1996-01-16 | 1997-07-17 | Bayer Ag | Pyrido-annellierte Thienyl- und Furanyl-Oxazolidinone |
HRP970049A2 (en) * | 1996-02-06 | 1998-04-30 | Bayer Ag | New heteroaryl oxazolidinones |
DE19604223A1 (de) * | 1996-02-06 | 1997-08-07 | Bayer Ag | Neue substituierte Oxazolidinone |
FR2744918B1 (fr) | 1996-02-19 | 1998-05-07 | Sanofi Sa | Nouvelles associations de principes actifs contenant un derive de thieno(3,2-c)pyridine et un antithrombotique |
DE19747261A1 (de) * | 1997-10-25 | 1999-04-29 | Bayer Ag | Osmotisches Arzneimittelfreisetzungssystem |
US20010029351A1 (en) * | 1998-04-16 | 2001-10-11 | Robert Falotico | Drug combinations and delivery devices for the prevention and treatment of vascular disease |
CA2327100A1 (en) * | 1998-05-18 | 1999-11-25 | Pharmacia & Upjohn Company | Enhancement of oxazolidinone antibacterial agents activity by using arginine derivatives |
DE19842753A1 (de) * | 1998-09-18 | 2000-03-23 | Bayer Ag | Agitationsunabhängige pharmazeutische Retardzubereitungen und Verfahren zu ihrer Herstellung |
DE19962924A1 (de) * | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
AU2225901A (en) * | 1999-12-28 | 2001-07-09 | Ajinomoto Co., Inc. | Aspartame derivative crystals |
DE10105989A1 (de) * | 2001-02-09 | 2002-08-14 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
DE10110438A1 (de) * | 2001-03-05 | 2002-09-19 | Bayer Ag | Substituierte 2-Oxy-3,5-dicyano-4-aryl-6-aminopyridine und ihre Verwendung |
DE10110754A1 (de) * | 2001-03-07 | 2002-09-19 | Bayer Ag | Substituierte 2-Thio-3,5-dicyano-4-aryl-6-aminopyridine und ihre Verwendung |
DE10110747A1 (de) * | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte 2,6-Diamino-3,5-dicyano-4-aryl-pyridine und ihre Verwendung |
DE10115922A1 (de) * | 2001-03-30 | 2002-10-10 | Bayer Ag | Cyclisch substituierte 2-Thio-3,5-dicyano-4-aryl-6-aminopyridine und ihre Verwendung |
DE10115945A1 (de) * | 2001-03-30 | 2002-10-02 | Bayer Ag | Substituierte 2-Carba-3,5-dicyano-4-aryl-6-aminopyridine und ihre Verwendung |
DE10129725A1 (de) | 2001-06-20 | 2003-01-02 | Bayer Ag | Kombinationstherapie substituierter Oxazolidinone |
PL204653B1 (pl) | 2001-09-21 | 2010-01-29 | Bristol Myers Squibb Co | Pochodna pirazolo [3, 4-c] pirydyny, jej zastosowanie i kompozycja farmaceutyczna |
DE10152460A1 (de) * | 2001-10-24 | 2003-05-08 | Bayer Ag | Stents |
DE10238113A1 (de) * | 2001-12-11 | 2003-06-18 | Bayer Ag | Substituierte 2-Thio-3,5-dicyano-4-phenyl-6-aminopyridine und ihre Verwendung |
US20030161882A1 (en) * | 2002-02-01 | 2003-08-28 | Waterman Kenneth C. | Osmotic delivery system |
WO2004031143A2 (en) | 2002-10-02 | 2004-04-15 | Bristol-Myers Squibb Company | Novel combination of a factor xa inhibitor and clopidogrel |
DE10300111A1 (de) * | 2003-01-07 | 2004-07-15 | Bayer Healthcare Ag | Verfahren zur Herstellung von 5-Chlor-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)-phenyl]-1,3-oxazolidin-5-yl}-methyl)-2-thiophencarboxamid |
DE10355461A1 (de) * | 2003-11-27 | 2005-06-23 | Bayer Healthcare Ag | Verfahren zur Herstellung einer festen, oral applizierbaren pharmazeutischen Zusammensetzung |
DE102004002044A1 (de) * | 2004-01-15 | 2005-08-04 | Bayer Healthcare Ag | Herstellverfahren |
JP2008517974A (ja) | 2004-10-25 | 2008-05-29 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 抗血栓薬と併用しての血栓塞栓性疾患の治療および予防のためのジピリダモールの使用 |
DE102004062475A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Healthcare Ag | Feste, oral applizierbare pharmazeutische Darreichungsformen mit modifizierter Freisetzung |
US20060222640A1 (en) | 2005-03-29 | 2006-10-05 | Boehringer Ingelheim International Gmbh | New pharmaceutical compositions for treatment of thrombosis |
DE102006051625A1 (de) | 2006-11-02 | 2008-05-08 | Bayer Materialscience Ag | Kombinationstherapie substituierter Oxazolidinone |
-
2006
- 2006-11-02 DE DE102006051625A patent/DE102006051625A1/de not_active Withdrawn
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2007
- 2007-10-19 KR KR1020097008977A patent/KR20090086973A/ko not_active Application Discontinuation
- 2007-10-19 JP JP2009535588A patent/JP5379012B2/ja active Active
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- 2007-10-19 WO PCT/EP2007/009068 patent/WO2008052671A2/de active Application Filing
- 2007-10-19 CN CN2007800491463A patent/CN101610767B/zh active Active
- 2007-10-19 LT LTEP07819133.5T patent/LT2099453T/lt unknown
- 2007-10-19 SI SI200731973T patent/SI2099453T1/sl unknown
- 2007-10-19 ES ES07819133.5T patent/ES2644489T3/es active Active
- 2007-10-19 CA CA2668068A patent/CA2668068C/en active Active
- 2007-10-19 HU HUE07819133A patent/HUE034869T2/en unknown
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- 2007-10-19 DK DK07819133.5T patent/DK2099453T3/da active
- 2007-10-19 US US12/513,363 patent/US20100120718A1/en not_active Abandoned
- 2007-10-19 EP EP07819133.5A patent/EP2099453B1/de not_active Revoked
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- 2016-06-23 US US15/190,944 patent/US20160303138A1/en not_active Abandoned
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- 2017-10-20 CY CY20171101097T patent/CY1119546T1/el unknown
-
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- 2018-02-06 LU LU00063C patent/LUC00063I2/fr unknown
- 2018-02-08 LT LTPA2018006C patent/LTPA2018006I1/lt unknown
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Cited By (11)
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CN104693139A (zh) * | 2011-01-07 | 2015-06-10 | 浙江九洲药业股份有限公司 | 一种合成利伐沙班中间体的新工艺 |
CN104693139B (zh) * | 2011-01-07 | 2017-04-19 | 浙江九洲药业股份有限公司 | 一种合成利伐沙班中间体的新工艺 |
CN102796091A (zh) * | 2011-05-24 | 2012-11-28 | 北大方正集团有限公司 | 取代的噁唑烷酮化合物及其制备方法和应用 |
CN102746287A (zh) * | 2012-06-21 | 2012-10-24 | 成都苑东药业有限公司 | 一种恶唑烷酮化合物及其制备方法 |
CN104086539A (zh) * | 2014-07-17 | 2014-10-08 | 天津炜捷制药有限公司 | 一种利伐沙班的制备方法 |
CN104402876A (zh) * | 2014-11-25 | 2015-03-11 | 沈阳药科大学 | 噁唑烷酮类化合物及其应用 |
CN104447728A (zh) * | 2014-12-05 | 2015-03-25 | 广东东阳光药业有限公司 | 噁唑烷酮类化合物及其在药物中的应用 |
CN104447730A (zh) * | 2014-12-05 | 2015-03-25 | 广东东阳光药业有限公司 | 噁唑烷酮类化合物及其在药物中的应用 |
CN104478866A (zh) * | 2014-12-05 | 2015-04-01 | 广东东阳光药业有限公司 | 噁唑烷酮类化合物及其在药物中的应用 |
CN104497008A (zh) * | 2014-12-09 | 2015-04-08 | 广东东阳光药业有限公司 | 取代噁唑烷酮类化合物及其使用方法和用途 |
CN104557900A (zh) * | 2014-12-23 | 2015-04-29 | 中国药科大学 | 噁唑烷酮类化合物及其制备方法与医药用途 |
Also Published As
Publication number | Publication date |
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CY2018004I1 (el) | 2018-09-05 |
EP2099453A2 (de) | 2009-09-16 |
KR20090086973A (ko) | 2009-08-14 |
LUC00063I2 (zh) | 2018-03-28 |
DK2099453T3 (da) | 2017-11-06 |
JP5379012B2 (ja) | 2013-12-25 |
ES2644489T3 (es) | 2017-11-29 |
US20160303138A1 (en) | 2016-10-20 |
DE102006051625A8 (de) | 2008-10-09 |
HUE034869T2 (en) | 2018-03-28 |
US20100120718A1 (en) | 2010-05-13 |
CY2018004I2 (el) | 2018-09-05 |
WO2008052671A2 (de) | 2008-05-08 |
LTPA2018006I1 (lt) | 2018-02-26 |
JP2010508366A (ja) | 2010-03-18 |
HUS1800011I1 (hu) | 2018-03-28 |
WO2008052671A3 (de) | 2008-07-03 |
EP2099453B1 (de) | 2017-09-06 |
DE102006051625A1 (de) | 2008-05-08 |
SI2099453T1 (sl) | 2017-11-30 |
CA2668068A1 (en) | 2008-05-08 |
CA2668068C (en) | 2013-12-17 |
CY1119546T1 (el) | 2018-03-07 |
PL2099453T3 (pl) | 2018-01-31 |
LT2099453T (lt) | 2017-11-10 |
PT2099453T (pt) | 2017-10-31 |
KR20150038742A (ko) | 2015-04-08 |
LUC00063I1 (zh) | 2018-02-12 |
CN101610767B (zh) | 2013-03-13 |
HK1139858A1 (en) | 2010-09-30 |
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