UY34023A - Derivados de fenil-isoxazol y procedimiento para la preparación de los mismos - Google Patents
Derivados de fenil-isoxazol y procedimiento para la preparación de los mismosInfo
- Publication number
- UY34023A UY34023A UY0001034023A UY34023A UY34023A UY 34023 A UY34023 A UY 34023A UY 0001034023 A UY0001034023 A UY 0001034023A UY 34023 A UY34023 A UY 34023A UY 34023 A UY34023 A UY 34023A
- Authority
- UY
- Uruguay
- Prior art keywords
- fenil
- isoxazol
- derivatives
- procedure
- preparation
- Prior art date
Links
- 241000950314 Figura Species 0.000 abstract 1
- FWYUJENICVGSJH-UHFFFAOYSA-M sodium;2-[bis[2-[2-(2-methyl-5-nitroimidazol-1-yl)ethoxy]-2-oxoethyl]amino]acetate Chemical compound [Na+].CC1=NC=C([N+]([O-])=O)N1CCOC(=O)CN(CC([O-])=O)CC(=O)OCCN1C([N+]([O-])=O)=CN=C1C FWYUJENICVGSJH-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- 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
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Se describe un compuesto derivado de fenil-isoxazol representado por la Fórmula 1 que se describe a continuación, que es útil como material de tratamiento para infecciones virales, especialmente la infección causada por un virus de la influenza, o su derivado farmacéuticamente aceptable, un método de preparación del mismo y una composición farmacéutica para el tratamiento de enfermedades, incluyendo el compuesto como principio activodonde en la fórmula citada anteriormente, R1, R2, R3, R4 y R8 son iguales a los que se define en la especificación.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020110036172A KR101369584B1 (ko) | 2011-04-19 | 2011-04-19 | 페닐-이속사졸 유도체 및 그의 제조방법 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY34023A true UY34023A (es) | 2012-06-29 |
Family
ID=46514985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY0001034023A UY34023A (es) | 2011-04-19 | 2012-04-16 | Derivados de fenil-isoxazol y procedimiento para la preparación de los mismos |
Country Status (21)
Country | Link |
---|---|
US (1) | US9132126B2 (es) |
EP (1) | EP2699566B1 (es) |
JP (1) | JP5833143B2 (es) |
KR (1) | KR101369584B1 (es) |
CN (1) | CN103313982B (es) |
AR (1) | AR086029A1 (es) |
AU (1) | AU2012246914B2 (es) |
CA (1) | CA2824757A1 (es) |
CL (1) | CL2013001910A1 (es) |
CO (1) | CO6771432A2 (es) |
EA (1) | EA022336B1 (es) |
HK (1) | HK1188998A1 (es) |
IL (1) | IL227711A0 (es) |
MX (1) | MX340098B (es) |
PE (1) | PE20140629A1 (es) |
SA (1) | SA112330457B1 (es) |
SG (1) | SG192134A1 (es) |
TW (1) | TWI434836B (es) |
UY (1) | UY34023A (es) |
WO (1) | WO2012144752A1 (es) |
ZA (1) | ZA201305277B (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018141854A1 (en) | 2017-02-02 | 2018-08-09 | Janssen Vaccines & Prevention B.V. | Piperazine derivatives for influenza virus inhibition |
CA3052353A1 (en) | 2017-02-02 | 2018-08-09 | Janssen Vaccines & Prevention B.V. | Piperazine derivatives for influenza virus inhibition |
RU2769317C2 (ru) * | 2017-02-08 | 2022-03-30 | Биотрон Лимитед | Способы лечения гриппа |
TWI765323B (zh) * | 2019-08-22 | 2022-05-21 | 大陸商四川海思科製藥有限公司 | 抗流感病毒化合物及其製備方法和用途 |
CN111704587B (zh) * | 2020-06-29 | 2023-04-07 | 遵义医科大学 | 一种三氟甲基化1,3-噁嗪类化合物的合成方法 |
CN112300147B (zh) * | 2020-11-19 | 2021-12-24 | 中国医学科学院医药生物技术研究所 | 一种吡啶类化合物及其制备方法和应用、药物组合物 |
CN116761605A (zh) | 2021-02-04 | 2023-09-15 | 四川海思科制药有限公司 | Ha抑制剂化合物的盐及晶型 |
Family Cites Families (24)
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GB8427618D0 (en) * | 1984-11-01 | 1984-12-05 | Shell Int Research | Anticoccidial compositions |
SK282950B6 (sk) | 1990-04-24 | 2003-01-09 | Biota Scientific Management Pty Ltd | Deriváty alfa-D-neuramínovej kyseliny, spôsob ich prípravy, ich použitie a farmaceutické prípravky na ich báze |
DE759917T1 (de) | 1995-02-27 | 1998-10-22 | Gilead Sciences Inc | Neue selektive inhibitoren viraler oder bakterieller neuraminidasen |
UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
ES2180456B1 (es) * | 2001-07-20 | 2004-05-01 | Laboratorios S.A.L.V.A.T., S.A. | Isoxazoles sustituidos y su utilizacion como antibioticos. |
JP2005510479A (ja) | 2001-10-12 | 2005-04-21 | オンコノバ・セラピューティックス・インコーポレーテッド | 置換イソオキサゾールおよび置換2−イソオキサゾリンを調製する方法 |
WO2004002965A1 (de) | 2002-06-29 | 2004-01-08 | Zentaris Gmbh | Aryl- und heteroarylcarbonylpiperazine und deren verwendung zur behandlung gutartiger und bösartiger tumorerkrankungen |
AU2003232650A1 (en) | 2003-05-06 | 2004-11-26 | Il Yang Pharm Co., Ltd. | N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof |
KR20050051729A (ko) | 2003-11-28 | 2005-06-02 | 일양약품주식회사 | 사이클로 옥시게나제-2 억제제인 페닐 헤테로사이클의제조방법 |
CN1687075A (zh) * | 2005-03-24 | 2005-10-26 | 天津药物研究院 | 3-苯基异噁唑-5-甲酰胺基取代β-内酰胺类衍生物及其用途 |
WO2007008541A2 (en) * | 2005-07-08 | 2007-01-18 | Kalypsys, Inc. | Cellular cholesterol absorption modifiers |
KR100674813B1 (ko) | 2005-08-05 | 2007-01-29 | 일양약품주식회사 | N-페닐-2-피리미딘-아민 유도체 및 그의 제조방법 |
CA2659155A1 (en) * | 2006-07-20 | 2008-01-24 | Amgen Inc. | Substituted azole aromatic heterocycles as inhibitors of 11.beta.-hsd-1 |
US8334385B2 (en) | 2007-11-02 | 2012-12-18 | Glenmark Generics Limited | Process for the preparation of R-sitagliptin and its pharmaceutically acceptable salts thereof |
US20090192326A1 (en) | 2007-11-13 | 2009-07-30 | Nurit Perlman | Preparation of sitagliptin intermediate |
JP2011507910A (ja) | 2007-12-21 | 2011-03-10 | ユニバーシティー オブ ロチェスター | 真核生物の寿命を変更するための方法 |
KR101044880B1 (ko) | 2008-06-12 | 2011-06-28 | 일양약품주식회사 | 항궤양제 화합물의 합성에 유용한 중간체의 제조방법 |
KR20100021321A (ko) | 2008-08-14 | 2010-02-24 | 일양약품주식회사 | Ν-페닐-2-피리미딘-아민 유도체의 제조방법 |
TW201107342A (en) * | 2009-05-20 | 2011-03-01 | Chimerix Inc | Compounds, compositions and methods for treating viral infection |
IN2012DN01254A (es) * | 2009-08-05 | 2015-05-15 | Versitech Ltd | |
GB2474748B (en) | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
RS53844B1 (en) * | 2010-09-08 | 2015-08-31 | Bristol-Myers Squibb Company | NEW PIPERAZINE ANALYSIS AS A WIDER ANTI-VIRUS MEDICINE AGAINST VIRUS INFLUENCE |
ES2564257T3 (es) | 2010-09-28 | 2016-03-21 | Bristol-Myers Squibb Company | Nuevos análogos de piperazina con grupos heteroarilo sustituidos como antivirales de amplio espectro de la gripe |
KR101956586B1 (ko) | 2012-03-27 | 2019-03-11 | 일양약품주식회사 | 약제학적 조성물 및 이의 제조방법 |
-
2011
- 2011-04-19 KR KR1020110036172A patent/KR101369584B1/ko not_active IP Right Cessation
-
2012
- 2012-03-30 EP EP12774858.0A patent/EP2699566B1/en not_active Not-in-force
- 2012-03-30 PE PE2013002002A patent/PE20140629A1/es not_active Application Discontinuation
- 2012-03-30 WO PCT/KR2012/002362 patent/WO2012144752A1/en active Application Filing
- 2012-03-30 MX MX2013007661A patent/MX340098B/es active IP Right Grant
- 2012-03-30 CN CN201280005377.5A patent/CN103313982B/zh not_active Expired - Fee Related
- 2012-03-30 AU AU2012246914A patent/AU2012246914B2/en not_active Ceased
- 2012-03-30 EA EA201300805A patent/EA022336B1/ru not_active IP Right Cessation
- 2012-03-30 TW TW101111335A patent/TWI434836B/zh not_active IP Right Cessation
- 2012-03-30 CA CA2824757A patent/CA2824757A1/en not_active Abandoned
- 2012-03-30 SG SG2013056734A patent/SG192134A1/en unknown
- 2012-03-30 JP JP2013551922A patent/JP5833143B2/ja not_active Expired - Fee Related
- 2012-03-30 US US13/979,743 patent/US9132126B2/en not_active Expired - Fee Related
- 2012-04-16 UY UY0001034023A patent/UY34023A/es not_active Application Discontinuation
- 2012-04-16 SA SA112330457A patent/SA112330457B1/ar unknown
- 2012-04-17 AR ARP120101314A patent/AR086029A1/es unknown
-
2013
- 2013-06-27 CL CL2013001910A patent/CL2013001910A1/es unknown
- 2013-07-12 ZA ZA2013/05277A patent/ZA201305277B/en unknown
- 2013-07-29 IL IL227711A patent/IL227711A0/en unknown
- 2013-08-16 CO CO13196001A patent/CO6771432A2/es unknown
-
2014
- 2014-03-03 HK HK14102103.4A patent/HK1188998A1/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP2699566B1 (en) | 2017-02-22 |
SA112330457B1 (ar) | 2015-08-19 |
IL227711A0 (en) | 2013-09-30 |
US9132126B2 (en) | 2015-09-15 |
MX340098B (es) | 2016-06-27 |
EP2699566A1 (en) | 2014-02-26 |
JP2014503601A (ja) | 2014-02-13 |
JP5833143B2 (ja) | 2015-12-16 |
HK1188998A1 (zh) | 2014-05-23 |
CL2013001910A1 (es) | 2014-04-21 |
CA2824757A1 (en) | 2012-10-26 |
TWI434836B (zh) | 2014-04-21 |
WO2012144752A1 (en) | 2012-10-26 |
SG192134A1 (en) | 2013-08-30 |
ZA201305277B (en) | 2014-09-25 |
EP2699566A4 (en) | 2014-09-03 |
NZ613314A (en) | 2015-09-25 |
CN103313982B (zh) | 2016-02-03 |
US20140031364A1 (en) | 2014-01-30 |
MX2013007661A (es) | 2013-08-12 |
AR086029A1 (es) | 2013-11-13 |
EA022336B1 (ru) | 2015-12-30 |
EA201300805A1 (ru) | 2013-11-29 |
KR20120118665A (ko) | 2012-10-29 |
AU2012246914B2 (en) | 2015-09-24 |
CO6771432A2 (es) | 2013-10-15 |
AU2012246914A1 (en) | 2013-08-15 |
CN103313982A (zh) | 2013-09-18 |
KR101369584B1 (ko) | 2014-03-06 |
PE20140629A1 (es) | 2014-05-22 |
TW201309658A (zh) | 2013-03-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20201019 |