BRPI0517272A - derivados de pirimidina bicìclicos de inibição de hiv - Google Patents
derivados de pirimidina bicìclicos de inibição de hivInfo
- Publication number
- BRPI0517272A BRPI0517272A BRPI0517272-1A BRPI0517272A BRPI0517272A BR PI0517272 A BRPI0517272 A BR PI0517272A BR PI0517272 A BRPI0517272 A BR PI0517272A BR PI0517272 A BRPI0517272 A BR PI0517272A
- Authority
- BR
- Brazil
- Prior art keywords
- substituted
- alkyl
- amino
- optionally substituted
- halo
- Prior art date
Links
- -1 bicyclic pyrimidine derivatives Chemical class 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 208000037357 HIV infectious disease Diseases 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 230000010076 replication Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/24—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one nitrogen and one sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
DERIVADOS DE PIRIMIDINA BICìCLICOS DE INIBIçãO DE HIV. Os inibidores de replicação de HIV de fórmula (I) N-óxidos, sais de adição farmaceuticamente aceitáveis, aminas quartenárias ou formas estereolsoméricas destes, em que -a=a-a =a¬ 4¬- é -GH=CH-CH=GH-, -N=CH-CHGH-, -N=CH-N=CH-, -NCH- CHN-, -N=N-CH=CH-; -b=b-b=b¬ 4¬- e -CH=CH-CH=CH-, -N=CH-CH=CH-, -N=GH-N=CH-, -N=CH-CH=N-, -N=N- GHCH-; n e m é 0,1, 2, 3 e em certos casos também 4; R¬1¬ é hidrogênio;arila; formila; C~ 1-6~alquilcarbonila; C~ 1-6~alquila opcionalmente substituida; C~ 1-6~alquilóxicarbonila; R é OH; halo; C~ 1-6~alquila opcionalmente substituida, C~ 2-6~alquenila ou C~ 2-6~alquinila; carbonila substituida; carboxila; CN; nitro; amino; amino substituído; polialometila; polialometiltio;-S(=O)~ p~R¬ 6¬ ; C(=NH)R¬ 6¬; R¬ 2a¬ é CN; amino; amino substituído; C~ 16~alquila opcionalmente substituida; halo; C~ 1-6~alquiIóxi opcionalmente substituído; carbonila substituida; -CH=N-NH-C(=O)-R¬ 16¬; C~ 1-6~alquilóxiC~ 1-6~aIquila opcionalmente substituida; C~ 2-6~alqueniía ou C~ 2-6~alquiniía substituida; -C(=N-O-R¬ 8¬)-C~ 1-4~alquila; R¬ 7¬ ou -X-R¬ 7¬; R¬ 3¬ é CN; amino; C~ 1-6~aIquila; halo; C~ 1-6~alquiíóxi opcionalmente substituído; carbonila substituida; -CH=N-NH-C(=O)-R¬ 16¬; C~ 1-6~alquiIa substituida; C~ 16~alquilóxiC~ 1-6~alquila opcionalmente substituida; C~ 2-6~alquenila ou C~ 2-6~alquinila substituida; -C(=N-O-R~ 8~)-C~ 1-4~alquila; R¬ 7¬; -X-R¬ 7¬; R¬ 4¬ é halo; OH; C~ 1-6~aIquiIa, C~ 2-6~alquenila ou C~ 2-6~alquinila opcionalmente substituida; C~ 3-7~acicloalquila; C~ 1-6~alquilóxi; CN; nitro; polialoC~ 1-6~alquila; poliaíoC~ 1-6~alquilóxi; carbonila substituida; formila; amino; mono- ou di(C~ 1-4~alquil)amino ou R¬ 7¬; -A-B- é -CR¬ 5¬=N-, -N=N-, -CH~ 2~-CH~ 2~-, -CS-NH-, -CO-N H-, -CH=CH-; composições farmacêuticas compreendem estes, métodos para a preparação destes compostos e composições; o emprego destes compostos para a prevenção ou o tratamento de infecção de HIV.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04105419 | 2004-10-29 | ||
| PCT/EP2005/055589 WO2006045828A1 (en) | 2004-10-29 | 2005-10-27 | Hiv inhibiting bicyclic pyrimidine derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0517272A true BRPI0517272A (pt) | 2008-10-07 |
Family
ID=34929789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0517272-1A BRPI0517272A (pt) | 2004-10-29 | 2005-10-27 | derivados de pirimidina bicìclicos de inibição de hiv |
Country Status (16)
| Country | Link |
|---|---|
| US (5) | US8153640B2 (pt) |
| EP (1) | EP1807430B1 (pt) |
| JP (1) | JP5118972B2 (pt) |
| KR (1) | KR20070085286A (pt) |
| CN (1) | CN101048410B (pt) |
| AR (1) | AR051410A1 (pt) |
| AU (1) | AU2005298637B8 (pt) |
| BR (1) | BRPI0517272A (pt) |
| CA (1) | CA2577588C (pt) |
| ES (1) | ES2508766T3 (pt) |
| IL (1) | IL180963A (pt) |
| MX (1) | MX2007005159A (pt) |
| RU (1) | RU2403254C2 (pt) |
| TW (1) | TW200630370A (pt) |
| WO (1) | WO2006045828A1 (pt) |
| ZA (1) | ZA200703444B (pt) |
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|---|---|---|---|---|
| DD21593A (pt) * | ||||
| DE21593C (de) | Dr. LÖWIG, Prof. in Breslau | Verfahren zur Darstellung von Aetznatron und Aetzkali durch Glühen von Strontiumcarbonat oder Kaliumcarbonat mit Eisenoxyd | ||
| US3459731A (en) | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
| JPS5962594A (ja) * | 1982-09-30 | 1984-04-10 | Ss Pharmaceut Co Ltd | 3,5―ジ置換―トリアゾロピリミジン誘導体 |
| BR9611562A (pt) | 1995-11-23 | 1999-03-02 | Janssen Pharmaceutica Nv | Misturas sólidas de ciclodextrinas preparadas via extrusão sob fusão |
| NO311614B1 (no) | 1996-10-01 | 2001-12-17 | Janssen Pharmaceutica Nv | Substituerte diamino-1,3,5-triazinderivater |
| EP0945447A1 (en) | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
| EA002973B1 (ru) | 1998-03-27 | 2002-12-26 | Янссен Фармацевтика Н.В. | Производные пиримидина в качестве ингибиторов репликации вируса иммунодефицита человека |
| SK287270B6 (sk) * | 1998-11-10 | 2010-05-07 | Janssen Pharmaceutica N. V. | Derivát pyrimidínu |
| AU783981C (en) | 2000-05-08 | 2007-05-03 | Janssen Pharmaceutica N.V. | HIV replication inhibitors |
| ES2314224T3 (es) * | 2002-03-07 | 2009-03-16 | F. Hoffmann-La Roche Ag | Inhibidores pirimidina y piridina biciclicos de p38 quinasa. |
| GB0219746D0 (en) * | 2002-08-23 | 2002-10-02 | Inst Of Ex Botany Ascr | Azapurine derivatives |
| MXPA05007503A (es) * | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
| MXPA05011710A (es) | 2003-05-05 | 2006-01-23 | Hoffmann La Roche | Derivados de pirimidina con actividad de crf. |
| AU2004260738B2 (en) | 2003-07-16 | 2009-07-16 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
| EP1781659B1 (en) | 2003-07-16 | 2008-11-05 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
| CN1918158B (zh) * | 2004-02-14 | 2011-03-02 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| WO2005107760A1 (en) | 2004-04-30 | 2005-11-17 | Irm Llc | Compounds and compositions as inducers of keratinocyte differentiation |
-
2005
- 2005-10-27 JP JP2007538423A patent/JP5118972B2/ja not_active Expired - Fee Related
- 2005-10-27 AU AU2005298637A patent/AU2005298637B8/en not_active Ceased
- 2005-10-27 RU RU2007119784/04A patent/RU2403254C2/ru active
- 2005-10-27 CN CN2005800369335A patent/CN101048410B/zh not_active Expired - Fee Related
- 2005-10-27 EP EP05801379.8A patent/EP1807430B1/en not_active Expired - Lifetime
- 2005-10-27 MX MX2007005159A patent/MX2007005159A/es active IP Right Grant
- 2005-10-27 US US11/718,181 patent/US8153640B2/en not_active Expired - Fee Related
- 2005-10-27 BR BRPI0517272-1A patent/BRPI0517272A/pt not_active Application Discontinuation
- 2005-10-27 ES ES05801379.8T patent/ES2508766T3/es not_active Expired - Lifetime
- 2005-10-27 WO PCT/EP2005/055589 patent/WO2006045828A1/en not_active Ceased
- 2005-10-27 KR KR1020077009261A patent/KR20070085286A/ko not_active Withdrawn
- 2005-10-27 CA CA2577588A patent/CA2577588C/en not_active Expired - Fee Related
- 2005-10-28 TW TW094137858A patent/TW200630370A/zh unknown
- 2005-10-31 AR ARP050104552A patent/AR051410A1/es not_active Application Discontinuation
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2007
- 2007-01-25 IL IL180963A patent/IL180963A/en active IP Right Grant
- 2007-04-26 ZA ZA200703444A patent/ZA200703444B/xx unknown
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2012
- 2012-03-02 US US13/410,779 patent/US9487518B2/en not_active Expired - Fee Related
-
2016
- 2016-08-19 US US15/241,615 patent/US9802943B2/en not_active Expired - Fee Related
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2017
- 2017-09-22 US US15/713,452 patent/US10077270B2/en not_active Expired - Fee Related
- 2017-09-22 US US15/713,404 patent/US10072015B2/en not_active Expired - Fee Related
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