AR066404A1 - Inhibidores no nucleosidos de transcriptasa inversa - Google Patents

Inhibidores no nucleosidos de transcriptasa inversa

Info

Publication number
AR066404A1
AR066404A1 ARP080101433A ARP080101433A AR066404A1 AR 066404 A1 AR066404 A1 AR 066404A1 AR P080101433 A ARP080101433 A AR P080101433A AR P080101433 A ARP080101433 A AR P080101433A AR 066404 A1 AR066404 A1 AR 066404A1
Authority
AR
Argentina
Prior art keywords
hydrogen
alkyl
ch2oc
oar
halogen
Prior art date
Application number
ARP080101433A
Other languages
English (en)
Inventor
Roland J Billedeau
Wylie Solang Palmer
Zachary Kevin Sweeney
Jeffrey Wu
Original Assignee
Hoffmann La Roche
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR066404A1 publication Critical patent/AR066404A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Los compuestos de la formula (1) inhiben la transcriptasa inversa del VIH-l y proporcionan un método para la prevencion y el tratamiento de las infecciones del VIH-l y el tratamiento del SIDA y/o del. ARC. La presente invencion se refiere, también a composiciones que contienen compuestos de la formula 1 utiles para la prevencion y tratamiento de las infecciones del VIH-l. Reivindicacion 1: Un compuesto de la formula (1) en la que: X es CH2 o NH; Y es CH2 u O, con la condicion de que por lo menos uno de X e Y sea CH2 y con la condicion adicional de que cuando X1 es CH, entonces o bien (i) R1 es OAr o C(=O)Ar o bien (ii) X es NH; X1 es N o CH; R1 es C(=O)Ar, OAr, fluor o hidrogeno; R2 es OAr, hidrogeno, halogeno, alquilo C1-6, alcoxi C1-6 o halogeno, o cicloalquilo C3-5; R3 y R4 son con independencia hidrogeno, C1-6, alcoxi C1-6 o cicloalquilo C3-5; Ra es hidrogeno, CH2OH, CH2OC(=O) (CH2)nC(=O)OH, en el que n es un numero de 2 a 5, CH2OC(=O)alquilo C1-6, o CH2OC(=O)- CHRbNH2 en el que Rb es fenilo o alquilo inferior C1-6; Ar es fenilo sustituido por 1-3 restos elegidos con independencia entre halogeno, ciano, haloalquilo C1-6 o alquilo C1-6 o sus sales farmacéuticamente aceptables.
ARP080101433A 2007-04-09 2008-04-07 Inhibidores no nucleosidos de transcriptasa inversa AR066404A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US92244907P 2007-04-09 2007-04-09
US96134607P 2007-07-20 2007-07-20

Publications (1)

Publication Number Publication Date
AR066404A1 true AR066404A1 (es) 2009-08-19

Family

ID=39798124

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080101433A AR066404A1 (es) 2007-04-09 2008-04-07 Inhibidores no nucleosidos de transcriptasa inversa

Country Status (15)

Country Link
US (1) US20080293664A1 (es)
EP (1) EP2134711A2 (es)
JP (1) JP2010523613A (es)
KR (1) KR20100015435A (es)
CN (1) CN101679414A (es)
AR (1) AR066404A1 (es)
AU (1) AU2008235549A1 (es)
BR (1) BRPI0810496A2 (es)
CA (1) CA2683046A1 (es)
CL (1) CL2008000996A1 (es)
IL (1) IL200886A0 (es)
MX (1) MX2009010932A (es)
PE (1) PE20090143A1 (es)
TW (1) TW200906410A (es)
WO (1) WO2008122534A2 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006078891A2 (en) * 2005-01-21 2006-07-27 Neurogen Corporation Imidazolylmethyl and pyrazolylmethyl heteroaryl derivatives
CA2705338A1 (en) * 2007-11-16 2009-05-22 Boehringer Ingelheim International Gmbh Inhibitors of human immunodeficiency virus replication
RU2495878C2 (ru) * 2007-12-21 2013-10-20 Ф.Хоффманн-Ля Рош Аг Гетероциклические антивирусные соединения
EP2593419A1 (en) 2010-07-15 2013-05-22 Albemarle Corporation Processes for producing 4-bromo-2-methoxybenzaldehyde
US9497234B2 (en) * 2012-12-27 2016-11-15 Facebook, Inc. Implicit social graph connections
TW201613919A (en) * 2014-07-02 2016-04-16 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0128287D0 (en) * 2001-11-26 2002-01-16 Smithkline Beecham Plc Novel method and compounds
GB0206723D0 (en) * 2002-03-21 2002-05-01 Glaxo Group Ltd Novel compounds
TW200505441A (en) * 2003-03-24 2005-02-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitorsⅠ
CN100469769C (zh) * 2003-03-24 2009-03-18 弗·哈夫曼-拉罗切有限公司 作为逆转录酶抑制剂的苄基-哒嗪酮
CN1934092A (zh) * 2004-03-23 2007-03-21 弗·哈夫曼-拉罗切有限公司 非核苷逆转录酶抑制剂
US7166738B2 (en) * 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US7625949B2 (en) * 2004-04-23 2009-12-01 Roche Palo Alto Llc Methods for treating retroviral infections
RU2394028C2 (ru) * 2004-07-27 2010-07-10 Ф.Хоффманн-Ля Рош Аг Производные бензилтриазолона в качестве ненуклеозидных ингибиторов обратной транскриптазы
AR057455A1 (es) * 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
WO2008019968A1 (en) * 2006-08-16 2008-02-21 F. Hoffmann-La Roche Ag Non-nucleoside reverse transcriptase inhibitors

Also Published As

Publication number Publication date
BRPI0810496A2 (pt) 2018-11-06
JP2010523613A (ja) 2010-07-15
MX2009010932A (es) 2009-10-29
EP2134711A2 (en) 2009-12-23
CL2008000996A1 (es) 2008-10-10
AU2008235549A1 (en) 2008-10-16
CA2683046A1 (en) 2008-10-16
IL200886A0 (en) 2010-05-17
TW200906410A (en) 2009-02-16
US20080293664A1 (en) 2008-11-27
WO2008122534A2 (en) 2008-10-16
PE20090143A1 (es) 2009-02-26
CN101679414A (zh) 2010-03-24
KR20100015435A (ko) 2010-02-12
WO2008122534A3 (en) 2009-02-05

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