BRPI0515935B8 - pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica - Google Patents

pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica

Info

Publication number
BRPI0515935B8
BRPI0515935B8 BRPI0515935A BRPI0515935A BRPI0515935B8 BR PI0515935 B8 BRPI0515935 B8 BR PI0515935B8 BR PI0515935 A BRPI0515935 A BR PI0515935A BR PI0515935 A BRPI0515935 A BR PI0515935A BR PI0515935 B8 BRPI0515935 B8 BR PI0515935B8
Authority
BR
Brazil
Prior art keywords
alkyl
optionally substituted
substituted
amino
alkyloxy
Prior art date
Application number
BRPI0515935A
Other languages
English (en)
Inventor
Heeres Jan
Emile Georges Guillemont Jérôme
Joannes Lewi Paulus
Original Assignee
Janssen Sciences Ireland Uc
Janssen R&D Ireland
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 Janssen Sciences Ireland Uc, Janssen R&D Ireland, Tibotec Pharm Ltd filed Critical Janssen Sciences Ireland Uc
Publication of BRPI0515935A publication Critical patent/BRPI0515935A/pt
Publication of BRPI0515935B1 publication Critical patent/BRPI0515935B1/pt
Publication of BRPI0515935B8 publication Critical patent/BRPI0515935B8/pt

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/50Three nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Abstract

pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv. inibidores de replicação de hiv da fórmula (i), n-óxidos, sais de adição farmaceuticamente aceitáveis, aminas quaternárias ou formas estereoisoméricas dos mesmos, em que: - a1 = a2 - a3 = a4 é -ch=ch=ch=ch-, -n=ch-ch=ch, -n=ch-n=ch-, -n=ch-ch=n, -n=n-ch=ch; -b1 = b2 - b3 = b4 é -ch=ch-ch=ch, -n=ch-ch=ch, -n=ch-n=ch, -n=ch-ch=n-, -n=n-ch=ch, -n=ch-ch=ch, -n=ch-n=ch, -n=ch-ch=n-, -n=n-ch=ch-; r1 é hidrogênio; arila; formila; c1-c6 alquila opcionalmente substituída; c1-c6 alquilóxicarbonila; r2 é oh; halo; c2-c6 alquinila opcionalmente substituída; carbonila substituída; carboxila; cn; nitro; amino; amino substituído; polihalometila; polihlometiltio; -s(=o)rr6; c(=nh)r6; r2a é cn;amino; amino substituído; c1-c6 alquila opcionalmente substituída; halo; c1-6 alquilóxi opcionalmente substituído carbonila substituída; -ch=n-nh-c(=o)-r16; c1-6 alquilóxi c1-6 alquila opcionalmente substituída; c2-6 alquenila ou c2-6 alquinila opcionalmente substituída; -c(=n-o-r8)-c1-4 alquila; r7 ou -x3-r7; x1 é -nr1 -, -o-, -c(=))-, ch2, -choh-, s-, -s(=o)-; r3 é cn; amino; c1-c6 alquila; halo; c1-c6 alquilóxi opcionalmente substituido; carbonila substituída; -ch=n-nh-c(=o)-r16; c1-c6 alquila substituída;c2-c6 alquenila ou c2-c6 alquinila opcionalmente substituída; -c(=n-o-r8)-c1-4 alquila; r7; -x3-r7; r4 é halo; oh; c1-6 alquila opcionalmente substituída; c2-6 alquenila ou c2-6 alquinila; c3-7 cicloalquila; c1-6 alquilóxi; cn; nitro; polihalo c1-6 alquila; polihalo c1-6 alquilóxi; carbonila substituída; formila; amino; mono- ou di(c1-4 alquil)amino ou r7; r5 é -y-cqh2q-l ou cqh2q-y-c2h2r-l; l é arila ou het; processos para o preparo desses compostos, composições farmacêuticas compreendendo esses compostos como ingredientes ativo e o uso desses compostos para a prevenção ou tratamento de infecção pelo hiv.
BRPI0515935A 2004-09-30 2005-09-29 pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica BRPI0515935B8 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04104814 2004-09-30
PCT/EP2005/054931 WO2006035068A2 (en) 2004-09-30 2005-09-29 Hiv inhibiting 5-carbo- or heterocyclic substituted pyrimidines

Publications (3)

Publication Number Publication Date
BRPI0515935A BRPI0515935A (pt) 2008-08-12
BRPI0515935B1 BRPI0515935B1 (pt) 2019-11-19
BRPI0515935B8 true BRPI0515935B8 (pt) 2021-05-25

Family

ID=34929640

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0515935A BRPI0515935B8 (pt) 2004-09-30 2005-09-29 pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica

Country Status (17)

Country Link
US (1) US7531548B2 (pt)
EP (1) EP1797048B1 (pt)
JP (1) JP5162245B2 (pt)
KR (1) KR20070057798A (pt)
CN (1) CN101031550B (pt)
AR (1) AR050970A1 (pt)
AT (1) ATE520672T1 (pt)
AU (1) AU2005288865B2 (pt)
BR (1) BRPI0515935B8 (pt)
CA (1) CA2573976C (pt)
ES (1) ES2371924T3 (pt)
IL (1) IL180760A (pt)
MX (1) MX2007003798A (pt)
RU (1) RU2403244C2 (pt)
TW (1) TW200626560A (pt)
WO (1) WO2006035068A2 (pt)
ZA (1) ZA200702655B (pt)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1656372E (pt) 2003-07-30 2013-06-27 Rigel Pharmaceuticals Inc Métodos para o tratamento ou prevenção de doenças autoimunes com compostos de 2,4-pirimidinadiamina
AU2005288864B2 (en) * 2004-09-30 2012-08-23 Janssen Sciences Ireland Uc HIV inhibiting 5-heterocyclyl pyrimidines
WO2006035069A1 (en) * 2004-09-30 2006-04-06 Tibotec Pharmaceuticals Ltd. Hiv inhibiting 5-substituted pyrimidines
US20070203161A1 (en) 2006-02-24 2007-08-30 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
NZ563454A (en) 2005-06-08 2011-03-31 Rigel Pharmaceuticals Inc 2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway
DE602007009508D1 (de) * 2006-03-30 2010-11-11 Little Island Co Cork Hiv-inhibierende 5-(hydroxymethylen- und aminomethylen) substituierte pyrimidine
US8933089B2 (en) 2006-03-30 2015-01-13 Janssen R & D Ireland HIV inhibiting 5-amido substituted pyrimidines
JP5415957B2 (ja) 2006-12-13 2014-02-12 エフ.ホフマン−ラ ロシュ アーゲー 非ヌクレオシド逆転写酵素阻害剤としての2−(ピペリジン−4−イル)−4−フェノキシ−又はフェニルアミノ−ピリミジン誘導体
CN101573343B (zh) * 2006-12-29 2016-02-24 爱尔兰詹森科学公司 抑制人免疫缺陷病毒的6-取代的嘧啶
AU2007341228B2 (en) * 2006-12-29 2013-04-18 Janssen Sciences Ireland Uc HIV inhibiting 5,6-substituted pyrimidines
WO2008118823A2 (en) * 2007-03-26 2008-10-02 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
DK2361248T3 (en) 2008-06-27 2019-01-14 Celgene Car Llc Heteroberl compounds and uses thereof
US11351168B1 (en) 2008-06-27 2022-06-07 Celgene Car Llc 2,4-disubstituted pyrimidines useful as kinase inhibitors
US8338439B2 (en) 2008-06-27 2012-12-25 Celgene Avilomics Research, Inc. 2,4-disubstituted pyrimidines useful as kinase inhibitors
AR074210A1 (es) 2008-11-24 2010-12-29 Boehringer Ingelheim Int Derivados de pirimidina como inhibidores de ptk2-quinasa
TW201024281A (en) 2008-11-24 2010-07-01 Boehringer Ingelheim Int New compounds
ES2659725T3 (es) 2009-05-05 2018-03-19 Dana-Farber Cancer Institute, Inc. Inhibidores de EGFR y procedimiento de tratamiento de trastornos
AP2858A (en) * 2009-06-22 2014-02-28 Emcure Pharmaceuticals Ltd Process for synthesis of a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor
EP3144298A1 (en) 2010-08-10 2017-03-22 Celgene Avilomics Research, Inc. Besylate salt of a btk inhibitor
JP5956999B2 (ja) 2010-11-01 2016-07-27 セルジーン アヴィロミクス リサーチ, インコーポレイテッド ヘテロアリール化合物およびその使用
MX2013004894A (es) 2010-11-01 2013-10-17 Celgene Avilomics Res Inc Compuestos heterociclicos y usos de los mismos.
US8796255B2 (en) 2010-11-10 2014-08-05 Celgene Avilomics Research, Inc Mutant-selective EGFR inhibitors and uses thereof
AR088570A1 (es) 2011-10-28 2014-06-18 Celgene Avilomics Res Inc Metodos para tratar una enfermedad o trastorno relacionado con la tirosina quinasa de bruton
JP6317319B2 (ja) 2012-03-15 2018-04-25 セルジーン シーエーアール エルエルシー 上皮成長因子受容体キナーゼ阻害剤の固体形態
MX356179B (es) 2012-03-15 2018-05-17 Celgene Avilomics Res Inc Sales de un inhibidor de cinasa del receptor del factor de crecimiento epidermico.
EP2935226A4 (en) 2012-12-21 2016-11-02 Celgene Avilomics Res Inc HETEROARYL COMPOUNDS AND USES THEREOF
CN105188371A (zh) 2013-02-08 2015-12-23 西建阿维拉米斯研究公司 Erk抑制剂及其用途
US9492471B2 (en) 2013-08-27 2016-11-15 Celgene Avilomics Research, Inc. Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase
US9415049B2 (en) 2013-12-20 2016-08-16 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
ES2741785T3 (es) 2014-08-13 2020-02-12 Celgene Car Llc Formas y composiciones de un inhibidor de ERK
WO2021167495A1 (en) 2020-02-19 2021-08-26 Pharmasyntez, Joint Stock Company Pyrimidine-based bicycles as antiviral agents for the treatment and prevention of hiv infection
US11351149B2 (en) 2020-09-03 2022-06-07 Pfizer Inc. Nitrile-containing antiviral compounds
KR20230155351A (ko) * 2022-05-03 2023-11-10 한국화학연구원 5-클로로-2,4-다이아미노피리미딘을 포함하는 키나아제 억제 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9012592D0 (en) * 1990-06-06 1990-07-25 Smithkline Beecham Intercredit Compounds
NO311614B1 (no) 1996-10-01 2001-12-17 Janssen Pharmaceutica Nv Substituerte diamino-1,3,5-triazinderivater
EP0945443B9 (en) * 1998-03-27 2003-08-13 Janssen Pharmaceutica N.V. HIV inhibiting pyrimidine derivatives
DE69943247D1 (de) * 1998-03-27 2011-04-14 Janssen Pharmaceutica Nv HIV hemmende Pyrimidin Derivate
EP0945447A1 (en) 1998-03-27 1999-09-29 Janssen Pharmaceutica N.V. Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections
PL204427B1 (pl) 1998-11-10 2010-01-29 Janssen Pharmaceutica Nv Hamująca replikację wirusa HIV pochodna pirymidyny, sposób jej wytwarzania i zastosowanie oraz kompozycja farmaceutyczna
GB9828511D0 (en) * 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
WO2001085700A2 (en) 2000-05-08 2001-11-15 Janssen Pharmaceutica N.V. Hiv replication inhibiting pyrimidines and triazines
ES2265450T3 (es) * 2000-12-21 2007-02-16 Vertex Pharmaceuticals Incorporated Compuestos de pirazol utiles como inhibidores de la proteina quinasa.
JO3429B1 (ar) * 2001-08-13 2019-10-20 Janssen Pharmaceutica Nv مشتقات برميدينات مثبطة فيروس الايدز
NZ539823A (en) * 2002-11-28 2008-04-30 Schering Aktiengessellschaft Chk-, Pdk- and Akt-inhibitory pyrimidines, their production and use as pharmaceutical agents

Also Published As

Publication number Publication date
CN101031550B (zh) 2015-05-27
AU2005288865A1 (en) 2006-04-06
TW200626560A (en) 2006-08-01
US7531548B2 (en) 2009-05-12
ES2371924T3 (es) 2012-01-11
IL180760A0 (en) 2007-06-03
WO2006035068A3 (en) 2006-08-31
EP1797048B1 (en) 2011-08-17
AR050970A1 (es) 2006-12-06
ATE520672T1 (de) 2011-09-15
JP5162245B2 (ja) 2013-03-13
IL180760A (en) 2013-02-28
MX2007003798A (es) 2007-04-23
US20070208022A1 (en) 2007-09-06
WO2006035068A2 (en) 2006-04-06
CN101031550A (zh) 2007-09-05
CA2573976C (en) 2014-04-29
CA2573976A1 (en) 2006-04-06
EP1797048A2 (en) 2007-06-20
AU2005288865B2 (en) 2012-07-19
KR20070057798A (ko) 2007-06-07
BRPI0515935A (pt) 2008-08-12
BRPI0515935B1 (pt) 2019-11-19
JP2008514680A (ja) 2008-05-08
RU2007116161A (ru) 2008-11-10
ZA200702655B (en) 2008-09-25
RU2403244C2 (ru) 2010-11-10

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Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2690 DE 26-07-2022 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.