ECSP22049160A - Derivados de bencimidazol - Google Patents
Derivados de bencimidazolInfo
- Publication number
- ECSP22049160A ECSP22049160A ECSENADI202249160A ECDI202249160A ECSP22049160A EC SP22049160 A ECSP22049160 A EC SP22049160A EC SENADI202249160 A ECSENADI202249160 A EC SENADI202249160A EC DI202249160 A ECDI202249160 A EC DI202249160A EC SP22049160 A ECSP22049160 A EC SP22049160A
- Authority
- EC
- Ecuador
- Prior art keywords
- benzimidazole derivatives
- benzimidazoles
- processes
- formula
- medicine
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- 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
-
- 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]
-
- 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
- C07D405/14—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 three or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La invenci?n se refiere a bencimidazoles de la F?rmula (I) y sales de estos aceptables desde el punto de vista farmac?utico, en donde R1 a R6 son como se definen en la descripci?n; a su uso en la medicina; a composiciones que los contienen; a procesos para su preparaci?n; y a intermediarios usados en dichos procesos. Los bencimidazoles de la F?rmula (I) son inhibidores de ITK y, por lo tanto, son potencialmente ?tiles en el tratamiento de diversos trastornos, que incluyen dermatitis at?pica.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962951030P | 2019-12-20 | 2019-12-20 | |
| US202063108602P | 2020-11-02 | 2020-11-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP22049160A true ECSP22049160A (es) | 2022-07-29 |
Family
ID=73856233
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSENADI202249160A ECSP22049160A (es) | 2019-12-20 | 2022-06-20 | Derivados de bencimidazol |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US11661419B2 (es) |
| EP (1) | EP4077316A1 (es) |
| JP (1) | JP2023507138A (es) |
| KR (1) | KR20220118525A (es) |
| CN (1) | CN115087655A (es) |
| AU (1) | AU2020405536B2 (es) |
| BR (1) | BR112022011838A2 (es) |
| CA (1) | CA3103120A1 (es) |
| CL (1) | CL2022001675A1 (es) |
| CO (1) | CO2022008313A2 (es) |
| CR (1) | CR20220299A (es) |
| DO (1) | DOP2022000130A (es) |
| EC (1) | ECSP22049160A (es) |
| IL (1) | IL293831B2 (es) |
| MX (1) | MX2022007518A (es) |
| PE (1) | PE20221916A1 (es) |
| PY (1) | PY2085970A (es) |
| TW (1) | TWI766484B (es) |
| UY (1) | UY38998A (es) |
| WO (1) | WO2021124155A1 (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2020408107B2 (en) | 2019-12-20 | 2026-04-23 | Nuevolution A/S | Compounds active towards nuclear receptors |
| KR20220130126A (ko) | 2019-12-20 | 2022-09-26 | 미라티 테라퓨틱스, 인크. | Sos1 억제제 |
| EP4263526A1 (en) * | 2020-12-15 | 2023-10-25 | Pfizer Inc. | Benzimidazole derivatives and their use as inhibitors of itk for the treatment of skin disease |
| CN114624358A (zh) * | 2022-03-11 | 2022-06-14 | 哈尔滨圣泰生物制药有限公司 | 一种地氯雷他定口服液的质量检测方法 |
| US20240423959A1 (en) * | 2022-06-21 | 2024-12-26 | Jjr&D, Llc | Topical benzimidazole formulations and methods for use in treating inflammatory dermatoses |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK0901786T3 (da) | 1997-08-11 | 2007-10-08 | Pfizer Prod Inc | Faste farmaceutiske dispersioner med foröget biotilgængelighed |
| GB9911053D0 (en) | 1999-05-12 | 1999-07-14 | Pharmacia & Upjohn Spa | 4,5,6,7-tetrahydroindazole derivatives process for their preparation and their use as antitumour agents |
| JP5039268B2 (ja) * | 2001-10-26 | 2012-10-03 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | ベンゾイミダゾールおよび類縁体および蛋白キナーゼ阻害剤としてのその使用 |
| FR2831536A1 (fr) | 2001-10-26 | 2003-05-02 | Aventis Pharma Sa | Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de kdr |
| JP2003231687A (ja) | 2002-02-04 | 2003-08-19 | Japan Tobacco Inc | ピラゾリル縮合環化合物及びその医薬用途 |
| US20050250829A1 (en) | 2004-04-23 | 2005-11-10 | Takeda San Diego, Inc. | Kinase inhibitors |
| US20060235013A1 (en) | 2005-04-14 | 2006-10-19 | Guy Georges | Tricyclic azole derivatives |
| GB0602178D0 (en) | 2006-02-03 | 2006-03-15 | Merck Sharp & Dohme | Therapeutic treatment |
| WO2008024981A1 (en) | 2006-08-24 | 2008-02-28 | Serenex, Inc. | Piperazine-substituted benzothiophenes for treatment of mental disorders |
| ATE522536T1 (de) | 2008-02-25 | 2011-09-15 | Hoffmann La Roche | Pyrrolopyrazin-kinasehemmer |
| KR101261514B1 (ko) | 2008-02-25 | 2013-05-07 | 에프. 호프만-라 로슈 아게 | 피롤로피라진 키나아제 저해제 |
| CA2716223A1 (en) | 2008-02-25 | 2009-09-03 | F. Hoffmann-La Roche Ag | Pyrrolopyrazine kinase inhibitors |
| EP2247593B1 (en) | 2008-02-25 | 2011-08-10 | F. Hoffmann-La Roche AG | Pyrrolopyrazine kinase inhibitors |
| CN101952295B (zh) | 2008-02-25 | 2013-11-20 | 霍夫曼-拉罗奇有限公司 | 吡咯并吡嗪激酶抑制剂 |
| EP2196458A1 (en) | 2008-12-10 | 2010-06-16 | Laboratorios Del. Dr. Esteve, S.A. | Process for obtaining enantiomerically enriched pyrazole derivatives |
| EP2202232A1 (en) | 2008-12-26 | 2010-06-30 | Laboratorios Almirall, S.A. | 1,2,4-oxadiazole derivatives and their therapeutic use |
| EP2292237A1 (en) | 2009-08-14 | 2011-03-09 | Laboratorios Del. Dr. Esteve, S.A. | Sigma ligands for the prevention or treatment of pain induced by chemotherapy |
| US8299070B2 (en) | 2009-11-25 | 2012-10-30 | Japan Tobacco Inc. | Indole compounds and pharmaceutical use thereof |
| EP2366702A1 (en) | 2010-03-18 | 2011-09-21 | Almirall, S.A. | New oxadiazole derivatives |
| US8481541B2 (en) | 2010-03-22 | 2013-07-09 | Hoffmann-La Roche Inc. | Pyrrolopyrazine kinase inhibitors |
| RU2012152354A (ru) | 2010-05-20 | 2014-06-27 | Ф. Хоффманн-Ля Рош Аг | Производные пирролопиразина в качестве ингибиторов syk и jak |
| CA2803056C (en) * | 2010-06-23 | 2017-05-16 | Hanmi Science Co., Ltd. | Fused pyrimidine derivatives for inhibition of tyrosine kinase activity |
| US9242981B2 (en) | 2010-09-16 | 2016-01-26 | Merck Sharp & Dohme Corp. | Fused pyrazole derivatives as novel ERK inhibitors |
| EP2455080A1 (en) | 2010-11-23 | 2012-05-23 | Almirall, S.A. | S1P1 receptor agonists for use in the treatment of multiple sclerosis |
| EP2455081A1 (en) | 2010-11-23 | 2012-05-23 | Almirall, S.A. | S1P1 receptor agonists for use in the treatment of crohn's disease |
| MA34948B1 (fr) | 2011-02-07 | 2014-03-01 | Plexxikon Inc | Composes et procedes de modulation de kinase, et leurs indications |
| ES2573336T3 (es) | 2011-08-12 | 2016-06-07 | F. Hoffmann-La Roche Ag | Compuestos de indazol, composiciones y métodos de uso |
| WO2013030138A1 (en) | 2011-09-01 | 2013-03-07 | F. Hoffmann-La Roche Ag | Pyrrolopyrazine kinase inhibitors |
| AR092088A1 (es) | 2012-08-10 | 2015-03-25 | Hoffmann La Roche | Compuestos de pirazol-carboxamida, composiciones y metodos de uso |
| WO2014041518A1 (en) | 2012-09-14 | 2014-03-20 | Glenmark Pharmaceuticals S.A. | Thienopyrrole derivatives as itk inhibitors |
| WO2014048939A1 (en) | 2012-09-26 | 2014-04-03 | F. Hoffmann-La Roche Ag | Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |
| CN103804364A (zh) | 2012-11-06 | 2014-05-21 | 韩冰 | 一类治疗缺血性脑损伤的化合物及其用途 |
| CN103800337A (zh) | 2012-11-07 | 2014-05-21 | 韩冰 | 一类治疗神经退行性疾病的化合物及其用途 |
| CN103804361A (zh) | 2012-11-07 | 2014-05-21 | 韩冰 | 一类治疗神经退行性疾病的化合物及其用途 |
| CN103804291A (zh) | 2012-11-07 | 2014-05-21 | 韩冰 | 一类治疗神经退行性疾病的化合物及其用途 |
| CN103800328A (zh) | 2012-11-07 | 2014-05-21 | 韩冰 | 一类治疗神经退行性疾病的化合物及其用途 |
| CN103800327A (zh) | 2012-11-09 | 2014-05-21 | 韩冰 | 一类治疗青光眼的化合物及其用途 |
| CN103800340A (zh) | 2012-11-09 | 2014-05-21 | 韩冰 | 一类治疗青光眼的化合物及其用途 |
| CN103804272A (zh) | 2012-11-14 | 2014-05-21 | 韩冰 | 一类具有神经保护作用的化合物及其用途 |
| CN103804363A (zh) | 2012-11-14 | 2014-05-21 | 韩冰 | 一类具有神经保护作用的化合物及其用途 |
| CN103804302A (zh) | 2012-11-14 | 2014-05-21 | 杨育新 | 一类治疗创伤性脑损伤疾病的化合物及其用途 |
| CN103804351A (zh) | 2012-11-14 | 2014-05-21 | 韩冰 | 一类具有神经保护作用的化合物及其用途 |
| CN104628657A (zh) | 2013-11-06 | 2015-05-20 | 韩冰 | 一类治疗缺血性脑损伤的化合物及其用途 |
| WO2016001341A1 (en) | 2014-07-03 | 2016-01-07 | F. Hoffmann-La Roche Ag | Sulfonylaminopyridine compounds, compositions and methods of use |
| US20170253577A1 (en) | 2014-07-04 | 2017-09-07 | Japan Tobacco Inc. | Method for producing indole compound |
| WO2016010108A1 (ja) | 2014-07-18 | 2016-01-21 | 塩野義製薬株式会社 | 含窒素複素環誘導体およびそれらを含有する医薬組成物 |
| CN105524067A (zh) | 2014-09-28 | 2016-04-27 | 江苏柯菲平医药股份有限公司 | 4-取代吡咯并[2,3-d]嘧啶化合物及其用途 |
| WO2016091916A1 (en) | 2014-12-10 | 2016-06-16 | F. Hoffmann-La Roche Ag | Pyrazolylaminopurines as itk inhibitors |
| WO2016115455A2 (en) | 2015-01-15 | 2016-07-21 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | 6-aryl-7-substituted-3-(1h-pyrazol-5-yl)-7h-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines as inhibitors of the stat3 pathway with anti-proliferative activity |
| TWI788830B (zh) | 2015-07-02 | 2023-01-01 | 瑞士商赫孚孟拉羅股份公司 | 雙環內醯胺及其使用方法 |
| JP7407705B2 (ja) | 2018-05-25 | 2024-01-04 | 日本たばこ産業株式会社 | インドール化合物を含む多発性硬化症の治療又は予防剤 |
| SMT202400314T1 (it) | 2018-05-25 | 2024-09-16 | Japan Tobacco Inc | Composto di indolo per trattare cistite interstiziale |
| JP7322007B2 (ja) | 2018-05-25 | 2023-08-07 | 日本たばこ産業株式会社 | インドール化合物を含むネフローゼ症候群の治療又は予防剤 |
| EP4263526A1 (en) * | 2020-12-15 | 2023-10-25 | Pfizer Inc. | Benzimidazole derivatives and their use as inhibitors of itk for the treatment of skin disease |
-
2020
- 2020-12-16 KR KR1020227025150A patent/KR20220118525A/ko not_active Withdrawn
- 2020-12-16 AU AU2020405536A patent/AU2020405536B2/en not_active Ceased
- 2020-12-16 EP EP20828341.6A patent/EP4077316A1/en not_active Withdrawn
- 2020-12-16 MX MX2022007518A patent/MX2022007518A/es unknown
- 2020-12-16 JP JP2022537036A patent/JP2023507138A/ja active Pending
- 2020-12-16 CN CN202080096751.1A patent/CN115087655A/zh active Pending
- 2020-12-16 CR CR20220299A patent/CR20220299A/es unknown
- 2020-12-16 PE PE2022001143A patent/PE20221916A1/es unknown
- 2020-12-16 WO PCT/IB2020/062036 patent/WO2021124155A1/en not_active Ceased
- 2020-12-16 BR BR112022011838A patent/BR112022011838A2/pt not_active Application Discontinuation
- 2020-12-16 IL IL293831A patent/IL293831B2/en unknown
- 2020-12-17 CA CA3103120A patent/CA3103120A1/en active Pending
- 2020-12-18 TW TW109144868A patent/TWI766484B/zh not_active IP Right Cessation
- 2020-12-18 US US17/126,358 patent/US11661419B2/en active Active
- 2020-12-18 PY PY202002085970A patent/PY2085970A/es unknown
- 2020-12-21 UY UY0001038998A patent/UY38998A/es not_active Application Discontinuation
-
2022
- 2022-06-14 CO CONC2022/0008313A patent/CO2022008313A2/es unknown
- 2022-06-17 CL CL2022001675A patent/CL2022001675A1/es unknown
- 2022-06-17 DO DO2022000130A patent/DOP2022000130A/es unknown
- 2022-06-20 EC ECSENADI202249160A patent/ECSP22049160A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PY2085970A (es) | 2022-06-20 |
| WO2021124155A1 (en) | 2021-06-24 |
| IL293831B2 (en) | 2024-02-01 |
| TWI766484B (zh) | 2022-06-01 |
| IL293831A (en) | 2022-08-01 |
| US20210188829A1 (en) | 2021-06-24 |
| MX2022007518A (es) | 2022-09-19 |
| AU2020405536B2 (en) | 2023-09-07 |
| BR112022011838A2 (pt) | 2022-08-30 |
| US11661419B2 (en) | 2023-05-30 |
| EP4077316A1 (en) | 2022-10-26 |
| CA3103120A1 (en) | 2021-06-20 |
| UY38998A (es) | 2021-07-30 |
| AU2020405536A1 (en) | 2022-07-14 |
| CO2022008313A2 (es) | 2022-07-08 |
| CL2022001675A1 (es) | 2023-03-17 |
| DOP2022000130A (es) | 2022-07-31 |
| JP2023507138A (ja) | 2023-02-21 |
| PE20221916A1 (es) | 2022-12-23 |
| CR20220299A (es) | 2022-08-05 |
| TW202130634A (zh) | 2021-08-16 |
| CN115087655A (zh) | 2022-09-20 |
| KR20220118525A (ko) | 2022-08-25 |
| IL293831B1 (en) | 2023-10-01 |
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