AR087184A1 - Derivados de azaindol utiles para tratar infecciones por hiv y composiciones farmaceuticas que los contienen - Google Patents
Derivados de azaindol utiles para tratar infecciones por hiv y composiciones farmaceuticas que los contienenInfo
- Publication number
- AR087184A1 AR087184A1 ARP120102550A ARP120102550A AR087184A1 AR 087184 A1 AR087184 A1 AR 087184A1 AR P120102550 A ARP120102550 A AR P120102550A AR P120102550 A ARP120102550 A AR P120102550A AR 087184 A1 AR087184 A1 AR 087184A1
- Authority
- AR
- Argentina
- Prior art keywords
- aryl
- group
- cycloalkyl
- alkyl
- heterocycle
- Prior art date
Links
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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicación 1: Un compuesto que comprende la estructura de la fórmula (1) o una sal farmacéuticamente aceptable del mismo, en donde: L es un enlazador que se selecciona a partir del grupo que consiste en un enlace directo, un alquileno C1-6 de cadena ramificada o recta, -SO2-, -C(O)NH-, y un resto de formula (2), en donde los grupos R9 y R10, junto con el átomo de carbono con el que están enlazados, pueden unirse opcionalmente entre sí para formar un cicloalquilo C3-7; R1 se selecciona a partir del alquilo C1-6 o cicloalquilo C3-7; R2 se selecciona a partir del grupo que consiste en -CO2R9, -C(O)R15 y los restos del grupo de formulas (3); R3 se selecciona a partir del grupo que consiste en alquilo C1-6, -OR10, R10(R14)q, tetrahidrofuranilo, oxetanilo, furanilo, dioxolanilo, piranilo, dioxanilo, dioxinilo, -O-cicloalquilo C3-7, y -cicloalquilo C3-7-(R10); R4 se selecciona a partir del grupo que consiste en arilo C5-15, cicloalquilo C3-7, heterociclo C2-9, y heteroarilo C2-9, en donde el heterociclo y el heteroarilo cada uno comprenden de uno a tres heteroátomos seleccionados a partir del S, N u O, y en donde cada grupo R4 está opcionalmente sustituido por uno a cuatro sustituyentes seleccionados a partir del R11; R5, R6, y R7 se seleccionan independientemente a partir del -H, alquilo C1-6, alcoxilo C1-6, halógeno, nitrilo, cicloalquilo C3-7, -OR10-arilo C5-15, -OR10R14, -OR10-arilo C5-15, -OR10-arilo C5-14-(R11)m, -OR9, -R10(Y)-(R12)n, -OR10R17, -R10R17, -R17R15, -OR10(R14)q, -OR10(Y), -OR10R18, -OSO2R15, -R15, -arilo C5-15, -(Y), -(Y)-(R12)n, -C(O)-(Y), -C(O)R15, -R10-arilo C5-15, -R10R15, y -arilo C5-14-R12, en donde R5 y R6, junto con los átomos de carbono con los que están enlazados, pueden unirse opcionalmente entre sí para formar un anillo de cicloalquilo C4-7, de heterociclo C2-9, o de arilo C5-15, o de una manera alternativa, cuando L es un enlace, R6 y R7, junto con los átomos de carbono con los que están enlazados, pueden unirse opcionalmente entre sí para formar un anillo de heterociclo C3-7 o de cicloalquilo C3-7; R9 se selecciona independientemente a partir del -H y alquilo C1-6; R10 es alquilo C1-6; R11, R12, y R13 se seleccionan independientemente a partir del grupo que consiste en alquilo C1-6, alcoxilo C1-6, butoxi-carbonilo, oxo, -R10OR10, halógeno, -R15, -R10(R14)q, -OR10(R14)q, -SO2R10 -C(O)R10, -C(O)R15, y -R10R17; R14 es halógeno; R15 es -N(R16)2; R16 se selecciona independientemente a partir del grupo que consiste en -H, alquilo C1-6, hidroxilo, -SO2R10, -SO2N(R10)2, -C(O)NHR10, -C(O)R18, y -arilo C5-14-(R11); R17 es -OR9; R18 es -CO2R9; Y se selecciona independientemente a partir del heterociclo C2-9 o heteroarilo C2-9, en donde cada uno tiene de uno a tres heteroátomos seleccionados a partir del S, N u O; m es cero o un entero seleccionado a partir del 1, 2, 3, ó 4; n es cero o un entero seleccionado a partir del 1, 2, ó 3; p es cero o un entero seleccionado a partir del 1, 2, ó 3; y q es un entero seleccionado a partir del 1, 2, ó 3.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161508197P | 2011-07-15 | 2011-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR087184A1 true AR087184A1 (es) | 2014-02-26 |
Family
ID=47519251
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP120102550A AR087184A1 (es) | 2011-07-15 | 2012-07-13 | Derivados de azaindol utiles para tratar infecciones por hiv y composiciones farmaceuticas que los contienen |
Country Status (8)
Country | Link |
---|---|
US (1) | US8609653B2 (es) |
EP (1) | EP2731436B1 (es) |
JP (1) | JP6055468B2 (es) |
AR (1) | AR087184A1 (es) |
ES (1) | ES2624984T3 (es) |
TW (1) | TW201317237A (es) |
UY (1) | UY34201A (es) |
WO (1) | WO2013012649A1 (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2817896A1 (en) | 2010-11-15 | 2012-05-24 | Viiv Healthcare Uk Limited | Inhibitors of hiv replication |
EP2781519B1 (en) * | 2011-11-15 | 2019-10-30 | ST Pharm Co., Ltd. | Novel antiviral pyrrolopyridine derivative and a production method for same |
JP6129962B2 (ja) * | 2012-07-12 | 2017-05-17 | ヴィーブ ヘルスケア ユーケー リミテッド | 化合物及びhivを治療するための方法 |
TW201441197A (zh) | 2013-01-31 | 2014-11-01 | Shionogi & Co | Hiv複製抑制劑 |
EP2821082A1 (en) | 2013-07-05 | 2015-01-07 | Laboratoire Biodim | Method of producing an inactivated lentivirus, especially HIV, vaccine, kit and method of use |
EP3105236B1 (en) | 2014-02-12 | 2017-10-18 | ViiV Healthcare UK (No.5) Limited | Benzothiazole macrocycles as inhibitors of human immunodeficiency virus replication |
US9409922B2 (en) | 2014-02-18 | 2016-08-09 | Bristol-Myers Squibb Company | Imidazopyridine macrocycles as inhibitors of human immunodeficiency virus replication |
WO2015126743A1 (en) | 2014-02-18 | 2015-08-27 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
WO2015126758A1 (en) | 2014-02-18 | 2015-08-27 | Bristol-Myers Squibb Company | Imidazopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
US9273067B2 (en) | 2014-02-19 | 2016-03-01 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
CN103864661A (zh) * | 2014-04-01 | 2014-06-18 | 湖南华腾制药有限公司 | 一种2-氨基-3-氰基吡咯衍生物的合成工艺 |
WO2015174511A1 (ja) | 2014-05-16 | 2015-11-19 | 塩野義製薬株式会社 | Hiv複製阻害作用を有する3環性複素環誘導体 |
KR101592370B1 (ko) * | 2014-06-09 | 2016-02-11 | 한국화학연구원 | 신규한 피롤로피리딘 유도체 및 이의 hiv 저해제로서의 용도 |
RS57108B1 (sr) * | 2014-07-08 | 2018-06-29 | Viiv Healthcare Uk Ltd | Derivati izoindolina za upotrebu u lečenju virusne infekcije |
ES2703352T3 (es) | 2014-07-22 | 2019-03-08 | Viiv Healthcare Uk Ltd | Derivados de isoindolina útiles como agentes antivirales |
WO2016194806A1 (ja) | 2015-05-29 | 2016-12-08 | 塩野義製薬株式会社 | Hiv複製阻害作用を有する含窒素3環性誘導体 |
US20180170903A1 (en) * | 2015-07-06 | 2018-06-21 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
CA2991268A1 (en) | 2015-07-08 | 2017-01-12 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
SG10201912699RA (en) * | 2015-07-20 | 2020-02-27 | Genzyme Corp | Colony stimulating factor-1 receptor (csf-1r) inhibitors |
US20190284136A1 (en) | 2016-07-25 | 2019-09-19 | Viiv Healthcare Uk Limited | Indoline derivatives |
CN110461837B (zh) * | 2017-03-24 | 2022-06-17 | St制药株式会社 | 新型吡咯并吡啶衍生物、其制备方法及用途 |
TWI748194B (zh) | 2018-06-28 | 2021-12-01 | 德商菲尼克斯 Fxr有限責任公司 | 含有雙環核心部分之新穎lxr調節劑 |
KR20220023187A (ko) * | 2020-08-20 | 2022-03-02 | 에스티팜 주식회사 | 피롤로피리딘 유도체 및 이들의 용도 |
JP2024500919A (ja) | 2020-12-23 | 2024-01-10 | ジェンザイム・コーポレーション | 重水素化コロニー刺激因子-1受容体(csf-1r)阻害剤 |
CA3207714A1 (en) * | 2021-01-11 | 2022-07-14 | St Pharm Co., Ltd. | Pyrrolopyridine derivative preparation method |
CN113173884B (zh) * | 2021-05-06 | 2023-08-15 | 陕西师范大学 | 二氯二茂钛催化汉斯酯1,4-二氢吡啶类化合物合成吡啶及其衍生物的方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
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US4107288A (en) | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
JP2003503386A (ja) * | 1999-06-25 | 2003-01-28 | メルク エンド カムパニー インコーポレーテッド | 1−(芳香族またはヘテロ芳香族置換)−3−(ヘテロ芳香族置換)−1,3−プロパンジオン類およびそれの使用 |
US20040110785A1 (en) | 2001-02-02 | 2004-06-10 | Tao Wang | Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives |
KR20030093248A (ko) | 2001-03-19 | 2003-12-06 | 오노 야꾸힝 고교 가부시키가이샤 | 트리아자스피로[5.5]운데칸 유도체를 유효성분으로서함유하는 약제 |
EP1786813A2 (en) | 2004-09-03 | 2007-05-23 | Plexxikon, Inc. | Bicyclic heteroaryl pde4b inhibitors |
BRPI0819328A8 (pt) * | 2007-11-15 | 2016-02-10 | Boehringer Ingelheim Int | Compostos inibidores de replicação de vírus da imunodeficiência humana, composição farmacêutica e uso dos ditos compostos |
JP5269087B2 (ja) * | 2007-11-16 | 2013-08-21 | ギリアード サイエンシス インコーポレーテッド | ヒト免疫不全ウイルス複製のインヒビター |
EP2220046B1 (en) | 2007-11-16 | 2014-06-18 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
EP2640705A2 (en) * | 2010-11-15 | 2013-09-25 | Katholieke Universiteit Leuven | Novel antiviral compounds |
-
2012
- 2012-07-12 JP JP2014520296A patent/JP6055468B2/ja not_active Expired - Fee Related
- 2012-07-12 EP EP12814906.9A patent/EP2731436B1/en active Active
- 2012-07-12 ES ES12814906.9T patent/ES2624984T3/es active Active
- 2012-07-12 WO PCT/US2012/046354 patent/WO2013012649A1/en active Application Filing
- 2012-07-12 US US13/547,199 patent/US8609653B2/en not_active Expired - Fee Related
- 2012-07-13 AR ARP120102550A patent/AR087184A1/es not_active Application Discontinuation
- 2012-07-13 UY UY0001034201A patent/UY34201A/es not_active Application Discontinuation
- 2012-07-13 TW TW101125458A patent/TW201317237A/zh unknown
Also Published As
Publication number | Publication date |
---|---|
JP2014522858A (ja) | 2014-09-08 |
US8609653B2 (en) | 2013-12-17 |
EP2731436A1 (en) | 2014-05-21 |
EP2731436A4 (en) | 2015-03-11 |
EP2731436B1 (en) | 2017-03-08 |
TW201317237A (zh) | 2013-05-01 |
UY34201A (es) | 2013-02-28 |
US20130018049A1 (en) | 2013-01-17 |
JP6055468B2 (ja) | 2016-12-27 |
ES2624984T3 (es) | 2017-07-18 |
WO2013012649A1 (en) | 2013-01-24 |
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