MX2007005159A - Derivados de pirimidina biciclicos inhibidores del vih. - Google Patents
Derivados de pirimidina biciclicos inhibidores del vih.Info
- Publication number
- MX2007005159A MX2007005159A MX2007005159A MX2007005159A MX2007005159A MX 2007005159 A MX2007005159 A MX 2007005159A MX 2007005159 A MX2007005159 A MX 2007005159A MX 2007005159 A MX2007005159 A MX 2007005159A MX 2007005159 A MX2007005159 A MX 2007005159A
- Authority
- MX
- Mexico
- Prior art keywords
- substituted
- 6alkyl
- amino
- optionally substituted
- 6alkyloxy
- 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
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 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
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 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
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 208000037357 HIV infectious disease Diseases 0.000 abstract 1
- 150000001204 N-oxides Chemical class 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
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 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
Inhibidores de replicacion del VIH de formula (ve formula) N-oxidos, sales de adicion farmaceuticamente aceptables, aminas cuaternarias o sus formas estereoisomericas, en los cuales -a1=a2-a3=a4-es -CH=CH-CH=CH-, -N=CH-CH=CH-, -N=CH-N=CH-, -N=CH-CH=N, -N=N-CH=CH-; -b1=b2-b3=b4- es -CH=CH-CH=CH-, -N=CH-CH=CH-, -N=CH-N=CH-, -N=CH-CH=N, -N=N-CH=CH-; n y m es 0, 1, 2, 3 y en ciertos casos tambien 4,R1 es hidrogeno; arilo, formilo, alquilcarbonilo C1-6; alquilo C1-6 sustituido en forma opcional; alquiloxicarbonilo C1-6; R2 es OH; halogeno; alquilo C1-6 sustituido en forma opcional, alquenilo C2-6 o alquinilo C2-6; carbonilo sustituido; carboxilo; CN; nitro; amino; amino sustituido; polihalogenometilo; polihalogenometiltio; -S(=O)PR6, C(=NH)R6; R2a es CN; amino, amino sustituido, alquilo C1-6 sustituido en forma opcional; halogeno; alcoxi C1-6 sustituido en forma opcional; carbonilo sustituido; -CH=N-NH-C(=O)-R16; alquiloxi C1-6 sustituido en forma opcional; alquenilo C2-6 sustituido o alquinilo C2-6; -C(=N-O-R8)-alquilo C1-4; R7 o -X-R7; R3 es CN; amino; alquilo C1-6; halogeno; alquiloxi C1-6 sustituido en forma opcional; carbonilo sustituido; -CH=N-NH-C(=O)-R16; alquilo C1-6 sustituido; alquiloxi C1-6 alquilo C1-6 sustituido en forma opcional; alquenilo C2-6 sustituido o alquinilo C2-6; -C(=N-O-R8)-alquilo C1-4; R7; R4 es halogeno; OH; alquilo C1-6 sustituido en forma opcional, alquenilo C2-6 o alquinilo C2-6; cicloalquilo C3-7; alquiloxi C1-6; CON; nitro; polihalogenoalquilo C1-6; polihalogenoalquiloxi C1-6; carbonilo sustituido; formilo; amino; mono- o di(alquil C1-4-)amino o R7; -A-B- es -CR5=N-, -N=N-, -CH2-CH2-, -CS-NH-, -CO-NH-, -CH=CH-; composiciones farmaceuticas que los comprenden; metodos para la preparacion de estos compuestos y estas composiciones; el uso de estos compuestos para la prevencion o el tratamiento de la infeccion por VIH.
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 |
|---|---|
| MX2007005159A true MX2007005159A (es) | 2007-06-26 |
Family
ID=34929789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2007005159A MX2007005159A (es) | 2004-10-29 | 2005-10-27 | Derivados de pirimidina biciclicos inhibidores del vih. |
Country Status (16)
| Country | Link |
|---|---|
| US (5) | US8153640B2 (es) |
| EP (1) | EP1807430B1 (es) |
| JP (1) | JP5118972B2 (es) |
| KR (1) | KR20070085286A (es) |
| CN (1) | CN101048410B (es) |
| AR (1) | AR051410A1 (es) |
| AU (1) | AU2005298637B8 (es) |
| BR (1) | BRPI0517272A (es) |
| CA (1) | CA2577588C (es) |
| ES (1) | ES2508766T3 (es) |
| IL (1) | IL180963A (es) |
| MX (1) | MX2007005159A (es) |
| RU (1) | RU2403254C2 (es) |
| TW (1) | TW200630370A (es) |
| WO (1) | WO2006045828A1 (es) |
| ZA (1) | ZA200703444B (es) |
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|---|---|---|---|---|
| DD21593A (es) * | ||||
| 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 |
| CN1198655C (zh) | 1995-11-23 | 2005-04-27 | 詹森药业有限公司 | 通过熔体挤出法制备的环糊精固体混合物 |
| NO311614B1 (no) | 1996-10-01 | 2001-12-17 | Janssen Pharmaceutica Nv | Substituerte diamino-1,3,5-triazinderivater |
| HU230522B1 (hu) | 1998-03-27 | 2016-10-28 | Janssen Pharmaceutica N.V | HIV-gátló pirimidinszármazékok |
| EP0945447A1 (en) | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
| HU227453B1 (en) | 1998-11-10 | 2011-06-28 | Janssen Pharmaceutica Nv | Hiv replication inhibiting pyrimidines, and pharmaceutical compositions containing them |
| ES2542326T3 (es) | 2000-05-08 | 2015-08-04 | Janssen Pharmaceutica Nv | Inhibidores de la replicación del VIH |
| MXPA04008592A (es) * | 2002-03-07 | 2004-12-06 | Hoffmann La Roche | Inhibidores de piridina biciclica y pirimidina p38 cinasa. |
| GB0219746D0 (en) | 2002-08-23 | 2002-10-02 | Inst Of Ex Botany Ascr | Azapurine derivatives |
| JP2006516561A (ja) * | 2003-01-17 | 2006-07-06 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | 細胞増殖の阻害剤としての2−アミノピリジン置換ヘテロ環類 |
| CN100372851C (zh) | 2003-05-05 | 2008-03-05 | 弗·哈夫曼-拉罗切有限公司 | 具有crf活性的稠合的嘧啶衍生物 |
| US7449465B2 (en) | 2003-07-16 | 2008-11-11 | Janssen Pharmaceutica, N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
| BRPI0412596A (pt) * | 2003-07-16 | 2006-09-19 | Janssen Pharmaceutica Nv | derivados de triazolopirimidina como inibores de glicogênio sintase cinase 3 |
| DK1713806T3 (da) * | 2004-02-14 | 2013-08-05 | Irm Llc | Forbindelser og sammensætninger som proteinkinaseinhibitorer |
| WO2005107760A1 (en) * | 2004-04-30 | 2005-11-17 | Irm Llc | Compounds and compositions as inducers of keratinocyte differentiation |
-
2005
- 2005-10-27 AU AU2005298637A patent/AU2005298637B8/en not_active Ceased
- 2005-10-27 EP EP05801379.8A patent/EP1807430B1/en not_active Expired - Lifetime
- 2005-10-27 RU RU2007119784/04A patent/RU2403254C2/ru active
- 2005-10-27 MX MX2007005159A patent/MX2007005159A/es active IP Right Grant
- 2005-10-27 KR KR1020077009261A patent/KR20070085286A/ko not_active Withdrawn
- 2005-10-27 CN CN2005800369335A patent/CN101048410B/zh not_active Expired - Fee Related
- 2005-10-27 WO PCT/EP2005/055589 patent/WO2006045828A1/en not_active Ceased
- 2005-10-27 US US11/718,181 patent/US8153640B2/en not_active Expired - Fee Related
- 2005-10-27 ES ES05801379.8T patent/ES2508766T3/es not_active Expired - Lifetime
- 2005-10-27 JP JP2007538423A patent/JP5118972B2/ja not_active Expired - Fee Related
- 2005-10-27 CA CA2577588A patent/CA2577588C/en not_active Expired - Fee Related
- 2005-10-27 BR BRPI0517272-1A patent/BRPI0517272A/pt not_active Application Discontinuation
- 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
-
2012
- 2012-03-02 US US13/410,779 patent/US9487518B2/en not_active Expired - Fee Related
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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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