DE60329918D1 - Amidderivat - Google Patents
AmidderivatInfo
- Publication number
- DE60329918D1 DE60329918D1 DE60329918T DE60329918T DE60329918D1 DE 60329918 D1 DE60329918 D1 DE 60329918D1 DE 60329918 T DE60329918 T DE 60329918T DE 60329918 T DE60329918 T DE 60329918T DE 60329918 D1 DE60329918 D1 DE 60329918D1
- Authority
- DE
- Germany
- Prior art keywords
- amide derivative
- het
- halogen
- present
- formula
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 150000001408 amides Chemical class 0.000 title abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229940124290 BCR-ABL tyrosine kinase inhibitor Drugs 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic 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
- C07D239/28—Heterocyclic 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002189269 | 2002-06-28 | ||
| JP2002305146 | 2002-10-18 | ||
| JP2002377937 | 2002-12-26 | ||
| PCT/JP2003/008192 WO2004002963A1 (ja) | 2002-06-28 | 2003-06-27 | アミド誘導体及び医薬 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE60329918D1 true DE60329918D1 (de) | 2009-12-17 |
Family
ID=30003594
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60329918T Expired - Lifetime DE60329918D1 (de) | 2002-06-28 | 2003-06-27 | Amidderivat |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7494997B2 (de) |
| EP (1) | EP1533304B1 (de) |
| JP (1) | JP4552650B2 (de) |
| CN (1) | CN100343237C (de) |
| AT (1) | ATE447560T1 (de) |
| AU (1) | AU2003246100A1 (de) |
| BR (1) | BRPI0312288B8 (de) |
| CA (1) | CA2490907C (de) |
| DE (1) | DE60329918D1 (de) |
| DK (1) | DK1533304T3 (de) |
| ES (1) | ES2337995T3 (de) |
| MX (1) | MXPA04012845A (de) |
| PT (1) | PT1533304E (de) |
| RU (1) | RU2315043C2 (de) |
| WO (1) | WO2004002963A1 (de) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0215676D0 (en) | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
| US7375175B2 (en) | 2002-08-19 | 2008-05-20 | National Starch And Chemical Investment Holding Corporation | Dispersions containing living radicals |
| CA2513583C (en) * | 2003-01-17 | 2012-03-20 | Wisconsin Alumni Research Foundation | Modified retinoid compounds and their uses |
| GB2400101A (en) * | 2003-03-28 | 2004-10-06 | Biofocus Discovery Ltd | Compounds capable of binding to the active site of protein kinases |
| WO2004110452A1 (en) * | 2003-06-13 | 2004-12-23 | Novartis Ag | 2-aminopyrimidine derivatives as raf kinase inhibitors |
| WO2005019238A1 (ja) | 2003-08-22 | 2005-03-03 | Meiji Seika Kaisha, Ltd. | 新規アザライド及びアザラクタム誘導体とその製造法 |
| RU2410375C9 (ru) * | 2003-12-25 | 2017-08-02 | Ниппон Синяку Ко., Лтд. | Амидное производное и лекарственное средство |
| US8735415B2 (en) | 2004-09-09 | 2014-05-27 | Natco Pharma Limited | Acid addition salts of (3,5-Bis trifluoromethyl)-N-[4-methyl-3-(4-pyridin-3yl-pyrimidin-2ylamino)-phenyl]-benzamide |
| AU2005281299B2 (en) * | 2004-09-09 | 2012-03-15 | Natco Pharma Limited | Novel phenylaminopyrimidine derivatives as inhibitors of BCR-ABL kinase |
| GB0512091D0 (en) * | 2005-06-14 | 2005-07-20 | Novartis Ag | Organic compounds |
| KR100674813B1 (ko) * | 2005-08-05 | 2007-01-29 | 일양약품주식회사 | Ｎ-페닐-2-피리미딘-아민 유도체 및 그의 제조방법 |
| MX2009006536A (es) * | 2006-12-22 | 2009-06-26 | Novartis Ag | Compuestos de heteroaril-heteroarilo como inhibidores de cdk para el tratamiento de cancer, inflamacion e infecciones virales. |
| US8367686B2 (en) | 2007-06-07 | 2013-02-05 | Intra-Cellular Therapies, Inc. | Heterocycle compounds and uses thereof |
| US9062023B2 (en) | 2007-06-07 | 2015-06-23 | Intra-Cellular Therapies, Inc. | Heterocycle compounds and uses thereof |
| WO2009037247A1 (en) * | 2007-09-17 | 2009-03-26 | Neurosearch A/S | Pyrazine derivatives and their use as potassium channel modulators |
| US20090247767A1 (en) * | 2008-03-31 | 2009-10-01 | Teva Pharmaceutical Industries Ltd. | Processes for preparing sunitinib and salts thereof |
| BRPI1013366A2 (pt) | 2009-03-06 | 2016-03-29 | Novartis Ag | uso de derivados de pirimidilaminobenzamida para o tratamento de distúrbios mediados pela quinase contendo zíper de leucina e quinase contendo motivo alfa estéril (zak). |
| EP2461673A4 (de) | 2009-08-05 | 2013-08-07 | Intra Cellular Therapies Inc | Neue regulatorproteine und hemmer |
| KR20120099650A (ko) | 2009-10-23 | 2012-09-11 | 노파르티스 아게 | Ｂｃｒ-ａｂｌ, ｃ-ｋｉｔ, ｄｄｒ1, ｄｄｒ2 또는 ｐｄｇｆ-ｒ 키나제 활성에 의해 매개된 증식성 장애 및 다른 병적 상태의 치료 방법 |
| JO3634B1 (ar) | 2009-11-17 | 2020-08-27 | Novartis Ag | طريقة لعلاج اضطرابات تكاثرية وحالات مرضية أخرى متوسطة بنشاط كيناز bcr-abl، c-kit، ddr1، ddr2، أو pdgf-r |
| US9315481B2 (en) * | 2012-03-14 | 2016-04-19 | Indiana University Research And Technology Corporation | Compounds and methods for treating leukemia |
| CN104918919A (zh) | 2012-11-21 | 2015-09-16 | Ptc医疗公司 | 取代的反向嘧啶Bmi-1抑制剂 |
| NZ748260A (en) | 2013-08-30 | 2020-01-31 | Ptc Therapeutics Inc | Substituted pyrimidine bmi-1 inhibitors |
| WO2015076801A1 (en) * | 2013-11-21 | 2015-05-28 | Ptc Therapeutics, Inc. | Substituted triazine bmi-1 inhibitors |
| WO2015076800A1 (en) | 2013-11-21 | 2015-05-28 | Ptc Therapeutics, Inc. | Substituted pyridine and pyrazine bmi-1 inhibitors |
| WO2017156350A1 (en) | 2016-03-09 | 2017-09-14 | K-Gen, Inc. | Methods of cancer treatment |
| JP6778833B2 (ja) | 2017-01-20 | 2020-11-04 | 深▲チェン▼市塔吉瑞生物医薬有限公司Ｓｈｅｎｚｈｅｎ ＴａｒｇｅｔＲｘ， Ｉｎｃ． | キナーゼ活性を抑制するための（ヘテロ）アリールアミド類化合物 |
| WO2018133827A1 (zh) * | 2017-01-20 | 2018-07-26 | 深圳市塔吉瑞生物医药有限公司 | 用于抑制蛋白激酶活性的(杂)芳基酰胺类化合物 |
| EP3836932A2 (de) | 2018-08-17 | 2021-06-23 | PTC Therapeutics, Inc. | Verfahren zur behandlung von bauchspeicheldrüsenkrebs |
| AU2020232755A1 (en) * | 2019-03-05 | 2021-11-04 | Hongyi & Associates LLC. | Compounds for treating neurodegenerative diseases and cancers |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW225528B (de) * | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
| US5521184A (en) * | 1992-04-03 | 1996-05-28 | Ciba-Geigy Corporation | Pyrimidine derivatives and processes for the preparation thereof |
| CO4940418A1 (es) | 1997-07-18 | 2000-07-24 | Novartis Ag | Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso |
| GB0022438D0 (en) * | 2000-09-13 | 2000-11-01 | Novartis Ag | Organic Compounds |
-
2003
- 2003-06-27 MX MXPA04012845A patent/MXPA04012845A/es active IP Right Grant
- 2003-06-27 AT AT03738555T patent/ATE447560T1/de active
- 2003-06-27 EP EP03738555A patent/EP1533304B1/de not_active Expired - Lifetime
- 2003-06-27 CN CNB038201461A patent/CN100343237C/zh not_active Expired - Lifetime
- 2003-06-27 PT PT03738555T patent/PT1533304E/pt unknown
- 2003-06-27 US US10/519,722 patent/US7494997B2/en not_active Expired - Lifetime
- 2003-06-27 JP JP2004517313A patent/JP4552650B2/ja not_active Expired - Lifetime
- 2003-06-27 AU AU2003246100A patent/AU2003246100A1/en not_active Abandoned
- 2003-06-27 DK DK03738555.6T patent/DK1533304T3/da active
- 2003-06-27 CA CA2490907A patent/CA2490907C/en not_active Expired - Lifetime
- 2003-06-27 DE DE60329918T patent/DE60329918D1/de not_active Expired - Lifetime
- 2003-06-27 RU RU2005102098/04A patent/RU2315043C2/ru active
- 2003-06-27 WO PCT/JP2003/008192 patent/WO2004002963A1/ja not_active Ceased
- 2003-06-27 ES ES03738555T patent/ES2337995T3/es not_active Expired - Lifetime
- 2003-06-27 BR BRPI0312288A patent/BRPI0312288B8/pt active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| CA2490907C (en) | 2010-08-24 |
| JPWO2004002963A1 (ja) | 2005-10-27 |
| BRPI0312288B8 (pt) | 2021-05-25 |
| ATE447560T1 (de) | 2009-11-15 |
| AU2003246100A1 (en) | 2004-01-19 |
| EP1533304B1 (de) | 2009-11-04 |
| MXPA04012845A (es) | 2005-02-24 |
| JP4552650B2 (ja) | 2010-09-29 |
| CN1678590A (zh) | 2005-10-05 |
| RU2315043C2 (ru) | 2008-01-20 |
| WO2004002963A1 (ja) | 2004-01-08 |
| PT1533304E (pt) | 2010-02-08 |
| BR0312288A (pt) | 2005-04-12 |
| EP1533304A4 (de) | 2006-10-18 |
| BRPI0312288B1 (pt) | 2019-01-02 |
| US7494997B2 (en) | 2009-02-24 |
| EP1533304A1 (de) | 2005-05-25 |
| RU2005102098A (ru) | 2005-09-20 |
| DK1533304T3 (da) | 2010-03-22 |
| CN100343237C (zh) | 2007-10-17 |
| ES2337995T3 (es) | 2010-05-03 |
| CA2490907A1 (en) | 2004-01-08 |
| US20060014742A1 (en) | 2006-01-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |