AR099487A1 - Macrociclos de pirazolopirimidina como inhibidores de la replicación del virus de la inmunodeficiencia humana - Google Patents
Macrociclos de pirazolopirimidina como inhibidores de la replicación del virus de la inmunodeficiencia humanaInfo
- Publication number
- AR099487A1 AR099487A1 ARP150100473A ARP150100473A AR099487A1 AR 099487 A1 AR099487 A1 AR 099487A1 AR P150100473 A ARP150100473 A AR P150100473A AR P150100473 A ARP150100473 A AR P150100473A AR 099487 A1 AR099487 A1 AR 099487A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halo
- haloalkyl
- substituted
- hydrogen
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- 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
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/48—Oxygen atoms attached in position 4 having an acyclic carbon atom attached in position 4
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Medicinal Chemistry (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1) en donde: R¹ es alquilo o haloalquilo; R² es hidrógeno o alquilo; R³ es hidrógeno, halo o alquilo; R⁴ es hidrógeno, alquilo o cicloalquilo; R⁵ es hidrógeno, alquilo o (Ar⁴)alquilo; Ar¹ es fenilo o naftilo y se sustituye con 0 - 3 sustituyentes seleccionados de ciano, halo, alquilo, haloalquilo, alcoxi y haloalcoxi; Ar² es pirrolilo, pirazolilo o triazolilo sustituido con 0 - 2 sustituyentes de alquilo; Ar³ es fenilo sustituido con 0 - 3 sustituyentes seleccionados de ciano, halo, alquilo, haloalquilo, alcoxi y haloalcoxi; Ar⁴ es fenilo sustituido con 0 - 3 sustituyentes seleccionados de ciano, halo, alquilo, haloalquilo, alcoxi y haloalcoxi; X¹ es alquileno, alquenileno, -CH₂O-, -CH₂OCH₂-, -CH₂N(R⁴)CH₂- o -CH₂CON(R⁴)-; X² es -O-, -Ar¹-, -Ar²-, -CON(R⁵)-, -(Ar³)CH-, -((benciIoxi)CH₂)CH-, -O(Ar³)CH-, -CH₂CON(R⁵)- o -N(R⁵)COCON(R⁵)-; X³ está ausente o es -O-, alquiloxi, cicloalquiloxi, cicloalquilo, Ar³, (Ar³)O- o ((Ar³)alquil)O-; X⁴ es alquileno, alquenileno, alquilenoxi o alquenilenoxi; X⁵ está ausente o es -O-; y X⁶ es azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, homopiperidinilo, homopiperazinilo u homomorfolinilo, y se sustituye con 0 - 3 sustituyentes de halo o alquilo; o una sal de aquel aceptable desde el punto de vista farmacéutico.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461941931P | 2014-02-19 | 2014-02-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR099487A1 true AR099487A1 (es) | 2016-07-27 |
Family
ID=53797505
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150100473A AR099487A1 (es) | 2014-02-19 | 2015-02-18 | Macrociclos de pirazolopirimidina como inhibidores de la replicación del virus de la inmunodeficiencia humana |
Country Status (5)
Country | Link |
---|---|
US (1) | US9273067B2 (es) |
EP (1) | EP3107918A1 (es) |
AR (1) | AR099487A1 (es) |
TW (1) | TW201615644A (es) |
WO (1) | WO2015126737A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9932353B2 (en) * | 2014-02-18 | 2018-04-03 | Viiv Healthcare Uk (No. 5) Limited | Imidazopyrimidine 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 |
CA3124783A1 (en) * | 2018-12-27 | 2020-07-02 | Taisho Pharmaceutical Co., Ltd. | Pyrazolo[1,5-a]pyrimidine macrocyclic compound |
CN113773335A (zh) * | 2019-06-21 | 2021-12-10 | 成都海博为药业有限公司 | 一种作为蛋白质激酶抑制剂的化合物及其制备方法和用途 |
KR20220122637A (ko) | 2019-11-28 | 2022-09-02 | 바이엘 악티엔게젤샤프트 | 면역 활성화를 위한 dgk알파 억제제로서의 치환된 아미노퀴놀론 |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020055631A1 (en) | 2000-09-20 | 2002-05-09 | Augeri David J. | N-acylsulfonamide apoptosis promoters |
CN1980912A (zh) * | 2004-07-01 | 2007-06-13 | 第一制药株式会社 | 吡唑衍生物 |
US7939545B2 (en) | 2006-05-16 | 2011-05-10 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
EP2054416B8 (en) | 2006-08-04 | 2014-07-16 | Merz Pharma GmbH & Co. KGaA | Substituted pyrazolopyrimidines, a process for their preparation and their use as medicine |
US20080287479A1 (en) * | 2006-12-20 | 2008-11-20 | Pfizer Inc | Inhibitors of serine palmitoyltransferase |
WO2009062288A1 (en) | 2007-11-15 | 2009-05-22 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
US8377960B2 (en) | 2007-11-15 | 2013-02-19 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
WO2009062308A1 (en) | 2007-11-16 | 2009-05-22 | Boehringer Ingelheim International Gmbh | Inhibitors of human immunodeficiency virus replication |
EP2757096A1 (en) | 2007-11-16 | 2014-07-23 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
GB0908394D0 (en) | 2009-05-15 | 2009-06-24 | Univ Leuven Kath | Novel viral replication inhibitors |
JP2013515692A (ja) | 2009-12-23 | 2013-05-09 | カトリック・ユニベルシティト・ルーヴァン | 新規抗ウイルス化合物 |
KR20130135826A (ko) | 2010-07-02 | 2013-12-11 | 길리애드 사이언시즈, 인코포레이티드 | Aids를 치료하기 위한 나프트-2-일아세트산 유도체 |
CN103209963A (zh) | 2010-07-02 | 2013-07-17 | 吉里德科学公司 | 作为hiv抗病毒化合物的2-喹啉基-乙酸衍生物 |
US8633200B2 (en) | 2010-09-08 | 2014-01-21 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
AU2011331301A1 (en) | 2010-11-15 | 2013-05-23 | Katholieke Universiteit Leuven | Antiviral condensed heterocyclic compounds |
MX343274B (es) | 2010-11-15 | 2016-10-31 | Viiv Healthcare Uk Ltd | Inhibidores de la replicacion del vih. |
WO2013012649A1 (en) | 2011-07-15 | 2013-01-24 | Glaxosmithkline Llc | Azaindole compounds and methods for treating hiv |
US8791108B2 (en) | 2011-08-18 | 2014-07-29 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
ES2632443T3 (es) | 2011-09-22 | 2017-09-13 | Viiv Healthcare Uk Limited | Compuestos de pirrolopiridinona y procedimientos de tratamiento del VIH |
WO2013062028A1 (ja) | 2011-10-25 | 2013-05-02 | 塩野義製薬株式会社 | Hiv複製阻害剤 |
DK2781519T3 (da) | 2011-11-15 | 2019-12-16 | St Pharm Co Ltd | Nyt antiviralt pyrrolopyridinderivat og en produktionsmetode til samme |
US9034882B2 (en) | 2012-03-05 | 2015-05-19 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US9006235B2 (en) | 2012-03-06 | 2015-04-14 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US8906929B2 (en) | 2012-08-16 | 2014-12-09 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
US9663536B2 (en) | 2013-03-13 | 2017-05-30 | VIIV Healthcare UK (No.5) Limited | Inhibitors of human immunodeficiency virus replication |
EP2970297A1 (en) | 2013-03-14 | 2016-01-20 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
-
2015
- 2015-02-11 US US14/619,728 patent/US9273067B2/en not_active Expired - Fee Related
- 2015-02-13 EP EP15707834.6A patent/EP3107918A1/en not_active Withdrawn
- 2015-02-13 WO PCT/US2015/015742 patent/WO2015126737A1/en active Application Filing
- 2015-02-17 TW TW104105736A patent/TW201615644A/zh unknown
- 2015-02-18 AR ARP150100473A patent/AR099487A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
US20150232481A1 (en) | 2015-08-20 |
TW201615644A (zh) | 2016-05-01 |
EP3107918A1 (en) | 2016-12-28 |
WO2015126737A1 (en) | 2015-08-27 |
US9273067B2 (en) | 2016-03-01 |
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