PE20151249A1 - Derivados de pirazolopirimidina como inhibidores de jak quinasas - Google Patents
Derivados de pirazolopirimidina como inhibidores de jak quinasasInfo
- Publication number
- PE20151249A1 PE20151249A1 PE2015000692A PE2015000692A PE20151249A1 PE 20151249 A1 PE20151249 A1 PE 20151249A1 PE 2015000692 A PE2015000692 A PE 2015000692A PE 2015000692 A PE2015000692 A PE 2015000692A PE 20151249 A1 PE20151249 A1 PE 20151249A1
- Authority
- PE
- Peru
- Prior art keywords
- pyrazolo
- pyrazol
- carboxamide
- pyrimidine
- alkyl
- Prior art date
Links
- OGEBRHQLRGFBNV-RZDIXWSQSA-N chembl2036808 Chemical class C12=NC(NCCCC)=NC=C2C(C=2C=CC(F)=CC=2)=NN1C[C@H]1CC[C@H](N)CC1 OGEBRHQLRGFBNV-RZDIXWSQSA-N 0.000 title abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 102000015617 Janus Kinases Human genes 0.000 abstract 2
- 108010024121 Janus Kinases Proteins 0.000 abstract 2
- 125000006714 (C3-C10) heterocyclyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 208000032027 Essential Thrombocythemia Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000017733 acquired polycythemia vera Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 206010028537 myelofibrosis Diseases 0.000 abstract 1
- NFQKXDIBUBJLEU-UHFFFAOYSA-N n-[3-(2,5-dimethylphenyl)-1-methylpyrazol-4-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide Chemical compound CC1=CC=C(C)C(C=2C(=CN(C)N=2)NC(=O)C2=C3N=CC=CN3N=C2)=C1 NFQKXDIBUBJLEU-UHFFFAOYSA-N 0.000 abstract 1
- PBBLZBUJHLNSRL-UHFFFAOYSA-N n-[3-(5-chloro-2-methoxyphenyl)-1-methylpyrazol-4-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide Chemical compound COC1=CC=C(Cl)C=C1C1=NN(C)C=C1NC(=O)C1=C2N=CC=CN2N=C1 PBBLZBUJHLNSRL-UHFFFAOYSA-N 0.000 abstract 1
- FEHJLULEKAPKHV-UHFFFAOYSA-N n-[5-(5-chloro-2-methoxyphenyl)-1-methylpyrazol-4-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide Chemical compound COC1=CC=C(Cl)C=C1C(N(N=C1)C)=C1NC(=O)C1=C2N=CC=CN2N=C1 FEHJLULEKAPKHV-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 208000037244 polycythemia vera Diseases 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 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
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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
- A61K31/437—Heterocyclic 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 the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/06—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 linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Referida a un compuesto derivado de pirazolopirimidina de formula (I), donde R1 es H, alquilo C1-C6, OR6, NR6R7 o halogeno; R2 es un heteroarilo de 5 o 6 miembros opcionalmente sustituido con R4; R3 es fenilo, cicloalquilo C3-C6, heterociclilo de 3 a 10 miembros, entre otros; R4 es alquilo C1-C6, alquenilo C2-C6, alquinilo C2-C6, entre otros; R6 y R7 son H, alquilo C1-C6, alquinilo C2-C6, CN, entre otros. son compuestos preferidos: N-(3-(5-cloro-2-metoxifenil)-1-metil-1H-pirazol-4-il)pirazolo[1,5-a]pirimidina-3-carboxamida, N-(5-(5-cloro-2-metoxifenil)-1-metil-1H-pirazol-4-il)pirazolo[1,5-a]pirimidina-3-carboxamida, N-(3-(2,5-dimetilofenil)-1-metil-1H-pirazol-4-il)pirazolo[1,5-a]pirimidina-3-carboxamida, entre otros. Tambien esta referida a una composicion farmaceutica. Dichos compuestos inhiben una o mas janus quinasas, (JAK quinasas), y son utiles en el tratamiento de cancer, policitemia vera, mielofibrosis, enfermedad de Chron, artritis reumatoide, trombocitosis primaria, entre otros
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22291809P | 2009-07-02 | 2009-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20151249A1 true PE20151249A1 (es) | 2015-09-10 |
Family
ID=43411778
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2015000692A PE20151249A1 (es) | 2009-07-02 | 2010-07-02 | Derivados de pirazolopirimidina como inhibidores de jak quinasas |
PE2012000003A PE20120575A1 (es) | 2009-07-02 | 2010-07-02 | Derivados de pirazolopirimidina como inhibidores de jak quinasas |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2012000003A PE20120575A1 (es) | 2009-07-02 | 2010-07-02 | Derivados de pirazolopirimidina como inhibidores de jak quinasas |
Country Status (35)
Country | Link |
---|---|
US (6) | US8999998B2 (es) |
EP (3) | EP2448941B1 (es) |
JP (4) | JP5769261B2 (es) |
KR (3) | KR101903305B1 (es) |
CN (2) | CN104910161B (es) |
AU (1) | AU2010266188B2 (es) |
BR (1) | BRPI1010197A2 (es) |
CA (1) | CA2767097A1 (es) |
CL (1) | CL2012000001A1 (es) |
CO (1) | CO6491081A2 (es) |
CR (2) | CR20170115A (es) |
DK (1) | DK2448941T3 (es) |
EC (1) | ECSP12011645A (es) |
ES (1) | ES2657839T3 (es) |
HR (1) | HRP20180157T1 (es) |
HU (1) | HUE035537T2 (es) |
IL (3) | IL217224B (es) |
IN (1) | IN2012DN00755A (es) |
LT (1) | LT2448941T (es) |
MA (1) | MA33502B1 (es) |
MX (1) | MX2012000169A (es) |
MY (1) | MY160156A (es) |
NO (1) | NO2448941T3 (es) |
NZ (4) | NZ719972A (es) |
PE (2) | PE20151249A1 (es) |
PH (1) | PH12015500666A1 (es) |
PL (1) | PL2448941T3 (es) |
PT (1) | PT2448941T (es) |
RS (1) | RS56671B1 (es) |
RU (2) | RU2567238C2 (es) |
SG (2) | SG10201509607XA (es) |
SI (1) | SI2448941T1 (es) |
UA (1) | UA110324C2 (es) |
WO (1) | WO2011003065A2 (es) |
ZA (2) | ZA201200490B (es) |
Families Citing this family (124)
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LT2426129T (lt) | 2005-12-13 | 2017-02-10 | Incyte Holdings Corporation | Heteroarilu pakeisti pirolo[2,3-b]piridinai ir pirolo[2,3-b]pirimidinai kaip janus kinazės inhibitoriai |
RS54878B1 (sr) | 2007-06-13 | 2016-10-31 | Incyte Holdings Corp | Kristalne soli inhibitora janus kinaze (r)-3-(4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)-3-ciklopentilpropionitril |
RU2539568C2 (ru) | 2008-10-31 | 2015-01-20 | Дженентек, Инк. | Пиразолопиримидиновые соединения-ингибиторы jak и способы |
UA106078C2 (uk) | 2009-05-22 | 2014-07-25 | Інсайт Корпорейшн | 3-[4-(7H-ПІРОЛО[2,3-d]ПІРИМІДИН-4-ІЛ)-1H-ПІРАЗОЛ-1-ІЛ]ОКТАН- АБО ГЕПТАННІТРИЛ ЯК JAK-ІНГІБІТОРИ |
UA110324C2 (en) | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
MX364636B (es) | 2010-03-10 | 2019-05-03 | Incyte Corp | Derivados de piperidin-4-il azetidina como inhibidores de janus cinasa 1 (jak1). |
SG184475A1 (en) | 2010-04-07 | 2012-11-29 | Hoffmann La Roche | Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |
SI2574168T1 (sl) | 2010-05-21 | 2016-07-29 | Incyte Holdings Corporation | Topična formulacija zaviralca jak |
JP5985473B2 (ja) * | 2010-07-13 | 2016-09-06 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | IRAK4モジュレーターとしてのピラゾロ[1,5a]ピリミジン及びチエノ[3,2b]ピリミジン誘導体 |
AU2011323617B2 (en) | 2010-11-03 | 2015-02-05 | Corteva Agriscience Llc | Pesticidal compositions and processes related thereto |
US8609669B2 (en) | 2010-11-16 | 2013-12-17 | Abbvie Inc. | Potassium channel modulators |
SG190839A1 (en) | 2010-11-19 | 2013-07-31 | Incyte Corp | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
WO2012129258A1 (en) * | 2011-03-22 | 2012-09-27 | Merck Sharp & Dohme Corp. | Amidopyrazole inhibitors of interleukin receptor-associated kinases |
WO2012158399A1 (en) | 2011-05-13 | 2012-11-22 | Abbott Laboratories | Condensed 2 - carbamoylpyridazinones as potassium channel modulators |
AU2012273164B2 (en) | 2011-06-20 | 2015-05-28 | Incyte Holdings Corporation | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors |
US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
AU2012314518B2 (en) | 2011-09-27 | 2017-06-29 | F. Hoffmann-La Roche Ag | Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |
WO2013045653A1 (en) | 2011-09-30 | 2013-04-04 | Oncodesign S.A. | Macrocyclic flt3 kinase inhibitors |
ES2899850T3 (es) | 2011-10-26 | 2022-03-15 | Corteva Agriscience Llc | Composiciones plaguicidas y procedimientos relacionados con las mismas |
US9012443B2 (en) | 2011-12-07 | 2015-04-21 | Amgen Inc. | Bicyclic aryl and heteroaryl sodium channel inhibitors |
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EP2951590A1 (en) | 2013-02-04 | 2015-12-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
KR102366356B1 (ko) | 2013-03-06 | 2022-02-23 | 인사이트 홀딩스 코포레이션 | Jak 저해제를 제조하기 위한 방법 및 중간생성물 |
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- 2012-01-02 CL CL2012000001A patent/CL2012000001A1/es unknown
- 2012-01-20 ZA ZA2012/00490A patent/ZA201200490B/en unknown
- 2012-01-25 CO CO12011326A patent/CO6491081A2/es active IP Right Grant
- 2012-01-30 CR CR20120053A patent/CR20120053A/es unknown
- 2012-02-02 EC ECSP12011645 patent/ECSP12011645A/es unknown
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2013
- 2013-10-02 ZA ZA2013/07356A patent/ZA201307356B/en unknown
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2015
- 2015-02-06 US US14/615,873 patent/US20150152117A1/en not_active Abandoned
- 2015-03-25 PH PH12015500666A patent/PH12015500666A1/en unknown
- 2015-06-17 JP JP2015122441A patent/JP6312634B2/ja active Active
- 2015-12-09 IL IL242999A patent/IL242999B/en not_active IP Right Cessation
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2017
- 2017-06-20 US US15/627,847 patent/US20170283424A1/en not_active Abandoned
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2018
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- 2018-01-15 IL IL256921A patent/IL256921A/en unknown
- 2018-01-26 HR HRP20180157TT patent/HRP20180157T1/hr unknown
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2019
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2022
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2023
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