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BRPI0516746A - 5-heterociclil pirimidinas para inibição de hiv - Google Patents

5-heterociclil pirimidinas para inibição de hiv

Info

Publication number
BRPI0516746A
BRPI0516746A BRPI0516746-9A BRPI0516746A BRPI0516746A BR PI0516746 A BRPI0516746 A BR PI0516746A BR PI0516746 A BRPI0516746 A BR PI0516746A BR PI0516746 A BRPI0516746 A BR PI0516746A
Authority
BR
Brazil
Prior art keywords
substituted
optionally substituted
alkyl
amino
alkyloxy
Prior art date
Application number
BRPI0516746-9A
Other languages
English (en)
Inventor
Jerome Emile Georges Guillemont
Jan Heeres
Paulus Joannes Lewi
Original Assignee
Tibotec Pharm Ltd
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 Tibotec Pharm Ltd filed Critical Tibotec Pharm Ltd
Publication of BRPI0516746A publication Critical patent/BRPI0516746A/pt

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • 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
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D413/04—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 directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

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

Abstract

5-HETEROCICLIL PIRIMIDINAS PARA INIBIçãO DE HIV. Inibidores da replicação de HIV da fórmula (1), N-óxidos, sais de adição farmaceuticamente aceitáveis, aminas quaternárias ou formas estereoisoméricas dos mesmos, em que: a˜ = a - a = a¬ 4¬ é CH=CH-CH=CH-, -N=CH-CH=CH, -N=CH-N=CH-, -N=CH-CH=N, -N=N-CH=CH-; -b˜ = b - b = b¬ 4¬ é -CH=CH-CH=CH, -N=CH-CH=CH, -N=CH-N=CH, -N=CH-CH=N-, -N=N-CH=CH-; R˜ é hidrogênio; arila; formila; C~ 1~-C~ 6~ alquilcarbonila; C~ 1~-C~ 6~ alquila opcionalmente substituída; C~ 1~-C~ 6~ alquilóxicarbonila; R é OH; halo; C~ 2~-C~ 6~ alquenila ou C~ 2~-C~ 6~ alquinila opcionalmente substituída; carbonila substituída; carboxila; CN; nitro; amino;amino substituído; polihalometila; poilhalometiltio; -S(=O)rR¬ 6¬; C(=NH)R¬ 6¬; R¬ 2a¬ é CN; amino; amino substituído; C~ 1~-C~ 6~ alquila opcionalmente substituída; halo; C~ 1-6~ alquilóxi opcionalmente substituído; carbonila substituída; -CH=N-NH-C (=O)-R16; C~ 1-6~ alquilóxi C~ 1-6~ alquila opcionalmente substituída; C~ 2-6~ alquenila ou C~ 2-6~ alquinila opcionalmente substituída; -C(=N-O-R8)-C~ 1-4~ alquila; R¬ 7¬ ou X~ 1~ é -NR˜-,-O-, -C(=))-, CH~ 2~, -CHOH-,-S-, -S(=O)r-; R é CN; amino; C~ 1~-C~ 6~ alquila; halo; C~ 1~-C~ 6~ alquilóxi opcionalmente substituído; carbonila substituída; -CH=N-NH-C(=O)-R¬ 16¬; C~ 1~-C~ 6~ alquila substituída; C~ 1~-C~ 6~ alquilóxi C~ 1~-C~ 6~ alquila opcionalmente substituída; -C~ 2~-C~ 6~ alquenila ou C~ 2~ -C~ 6~ alquinila opcionalmente substituída; -C(=N-O-R¬ 8)-C~ 1-4~ alquila; R¬ 7¬; -X~ 3~-R¬ 7¬; R¬ 4¬ é halo; OH; C~ 1-6~ alquila opcionalmente substituída; C~ 2-6~ alquenila ou C~ 2-6~ alquinila; C~ 3-7 cicloalquila; C~ 1-6~ alquilóxi; CN; nitro; polihalo C~ 1-6~ alquila; polihalo C~ 1-6~ alquilóxi; carbonila substituída; formila; amino; mono- ou di(C~ 1-4~ alquil)amino ou R¬ 7¬; R¬ 5¬ é um sistema de anel completamente insaturado de 5 ou 6 elementos, em que 1-4 elementos no anel são nitrogênio, oxigênio ou enxofre; anel o qual pode ser opcionalmente substituído e pode ser opcionalmente anelado a um anel de benzeno; métodos para seu preparo e composições farmacêuticas compreendendo os mesmos. A presente invenção também se refere ao uso desses compostos para a prevenção ou tratamento de infecção pelo HIV.
BRPI0516746-9A 2004-09-30 2005-09-29 5-heterociclil pirimidinas para inibição de hiv BRPI0516746A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04104812 2004-09-30
PCT/EP2005/054930 WO2006035067A2 (en) 2004-09-30 2005-09-29 Hiv inhibiting 5-heterocyclyl pyrimidines

Publications (1)

Publication Number Publication Date
BRPI0516746A true BRPI0516746A (pt) 2008-09-23

Family

ID=34929638

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0516746-9A BRPI0516746A (pt) 2004-09-30 2005-09-29 5-heterociclil pirimidinas para inibição de hiv

Country Status (17)

Country Link
US (1) US8575342B2 (pt)
EP (1) EP1797069B1 (pt)
JP (1) JP5008567B2 (pt)
KR (1) KR20070057899A (pt)
CN (1) CN101031558B (pt)
AR (1) AR050969A1 (pt)
AT (1) ATE520680T1 (pt)
AU (1) AU2005288864B2 (pt)
BR (1) BRPI0516746A (pt)
CA (1) CA2577467C (pt)
ES (1) ES2371923T3 (pt)
IL (1) IL180959A (pt)
MX (1) MX2007003797A (pt)
RU (1) RU2405778C2 (pt)
TW (1) TW200626574A (pt)
WO (1) WO2006035067A2 (pt)
ZA (1) ZA200702653B (pt)

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BRPI0709690B8 (pt) 2006-03-30 2021-05-25 Janssen R & D Ireland 5-amido pirimidinas substituídas e composição farmacêutica que as compreende
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US10709708B2 (en) 2016-03-17 2020-07-14 The University Of North Carolina At Chapel Hill Method of treating cancer with a combination of MER tyrosine kinase inhibitor and an epidermal growth factor receptor (EGFR) inhibitor
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WO2019222538A1 (en) * 2018-05-16 2019-11-21 The University Of North Carolina At Chapel Hill Aminopyrimidines and aminopyridines as mertk inhibitors and their application in cancer treatment
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BRPI0709690B8 (pt) 2006-03-30 2021-05-25 Janssen R & D Ireland 5-amido pirimidinas substituídas e composição farmacêutica que as compreende
CN101573342A (zh) 2006-12-29 2009-11-04 泰博特克药品有限公司 抑制hiv的5,6-取代的嘧啶类化合物
KR20090094073A (ko) 2006-12-29 2009-09-03 티보텍 파마슈티칼즈 리미티드 Ｈｉｖ를 억제하는 6-치환된 피리미딘

Also Published As

Publication number Publication date
EP1797069B1 (en) 2011-08-17
KR20070057899A (ko) 2007-06-07
CN101031558A (zh) 2007-09-05
CA2577467C (en) 2013-05-28
RU2007116152A (ru) 2008-11-10
ZA200702653B (en) 2008-08-27
AU2005288864A1 (en) 2006-04-06
WO2006035067A2 (en) 2006-04-06
US20090181993A1 (en) 2009-07-16
WO2006035067A3 (en) 2006-08-24
IL180959A (en) 2012-08-30
TW200626574A (en) 2006-08-01
AR050969A1 (es) 2006-12-06
ES2371923T3 (es) 2012-01-11
MX2007003797A (es) 2007-04-23
RU2405778C2 (ru) 2010-12-10
CN101031558B (zh) 2011-10-05
ATE520680T1 (de) 2011-09-15
IL180959A0 (en) 2007-07-04
EP1797069A2 (en) 2007-06-20
CA2577467A1 (en) 2006-04-06
US8575342B2 (en) 2013-11-05
JP5008567B2 (ja) 2012-08-22
JP2008514679A (ja) 2008-05-08
AU2005288864B2 (en) 2012-08-23

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B25D Requested change of name of applicant approved

Owner name: TIBOTEC PHARMACEUTICALS (IE)

B25D Requested change of name of applicant approved

Owner name: JANSSEN R AND D IRELAND (IE)

B25A Requested transfer of rights approved

Owner name: JANSSEN SCIENCES IRELAND UC (IE)

B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]

Free format text: DE ACORDO COM O ARTIGO 229-C DA LEI NO 10196/2001, QUE MODIFICOU A LEI NO 9279/96, A CONCESSAO DA PATENTE ESTA CONDICIONADA A ANUENCIA PREVIA DA ANVISA. CONSIDERANDO A APROVACAO DOS TERMOS DO PARECER NO 337/PGF/EA/2010, BEM COMO A PORTARIA INTERMINISTERIAL NO 1065 DE 24/05/2012, ENCAMINHA-SE O PRESENTE PEDIDO PARA AS PROVIDENCIAS CABIVEIS.

B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]
B06U Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B11D Dismissal acc. art. 38, par 2 of ipl - failure to pay fee after grant in time