PE20091669A1 - Benzofuropirimidinonas - Google Patents
BenzofuropirimidinonasInfo
- Publication number
- PE20091669A1 PE20091669A1 PE2008002147A PE2008002147A PE20091669A1 PE 20091669 A1 PE20091669 A1 PE 20091669A1 PE 2008002147 A PE2008002147 A PE 2008002147A PE 2008002147 A PE2008002147 A PE 2008002147A PE 20091669 A1 PE20091669 A1 PE 20091669A1
- Authority
- PE
- Peru
- Prior art keywords
- benzofide
- ilmethyl
- pyrrolidin
- pyrimidin
- halo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
REFERIDA A UN COMPUESTO DE FORMULA I, DONDE R1 ES H, ALQUILO; R2 ES AMINOCARBONILALQUILAMINOALQUILO, CICLOALQUILAMINOALQUILO, ARILALQUILO, ENTRE OTROS; R3a ES HALO, ALQUILO, -NO2, ALCOXI, ALQUINILO SUSTITUIDO O NO, ALCOXICARBONILALQUILO, ENTRE OTROS; R3b, R3c Y R3d SON CADA UNO H, -OH, ALCOXILO, HALO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 8-BROMO-2-(PIRROLIDIN-1-ILMETIL)[1]BENZOFURO[3,2-d]PIRIMIDIN-4(3H)-ONA; 8-CLORO-2-(PIRROLIDIN-1-ILMETIL)[1]BENZOFURO[3,2-d]PIRIMIDIN-4(3H)-ONA; ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE PROTEINA QUINASA UTILES EN EL TRATAMIENTO DE CANCER
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US890707P | 2007-12-21 | 2007-12-21 | |
| US7097108P | 2008-03-25 | 2008-03-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20091669A1 true PE20091669A1 (es) | 2009-12-06 |
Family
ID=40383673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008002147A PE20091669A1 (es) | 2007-12-21 | 2008-12-19 | Benzofuropirimidinonas |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US20090247559A1 (es) |
| EP (1) | EP2097419B1 (es) |
| JP (1) | JP2011507908A (es) |
| KR (1) | KR20100098714A (es) |
| CN (1) | CN101965351A (es) |
| AR (1) | AR069869A1 (es) |
| AT (1) | ATE510839T1 (es) |
| AU (1) | AU2008345560A1 (es) |
| BR (1) | BRPI0821573A2 (es) |
| CA (1) | CA2712358A1 (es) |
| CL (1) | CL2008003873A1 (es) |
| CO (1) | CO6321258A2 (es) |
| EA (1) | EA019785B1 (es) |
| IL (1) | IL206416A0 (es) |
| MX (1) | MX2010006799A (es) |
| NZ (1) | NZ586936A (es) |
| PE (1) | PE20091669A1 (es) |
| TW (1) | TW200930375A (es) |
| WO (1) | WO2009086264A1 (es) |
| ZA (1) | ZA201004243B (es) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102007061963A1 (de) | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008028905A1 (de) | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
| WO2010064146A2 (en) | 2008-12-02 | 2010-06-10 | Chiralgen, Ltd. | Method for the synthesis of phosphorus atom modified nucleic acids |
| MY160526A (en) | 2008-12-22 | 2017-03-15 | Merck Patent Gmbh | Novel polymorphic forms of 6-(1-methyl-1h-pyrazol-4-yl)-2-{3-[5-(2-morpholin-4-yl-ethoxy)-pyrimidin-2-yl]-benzyl}-2h-pyridazin-3-one dihydrogenphosphate and processes of manufacturing thereof |
| CA2767253A1 (en) | 2009-07-06 | 2011-01-13 | Ontorii, Inc. | Novel nucleic acid prodrugs and methods of use thereof |
| WO2012039448A1 (ja) * | 2010-09-24 | 2012-03-29 | 株式会社キラルジェン | 不斉補助基 |
| CN103796657B (zh) | 2011-07-19 | 2017-07-11 | 波涛生命科学有限公司 | 合成官能化核酸的方法 |
| CA2879066C (en) | 2012-07-13 | 2019-08-13 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant |
| JP6453212B2 (ja) | 2012-07-13 | 2019-01-16 | ウェイブ ライフ サイエンシズ リミテッドWave Life Sciences Ltd. | キラル制御 |
| WO2014010250A1 (en) | 2012-07-13 | 2014-01-16 | Chiralgen, Ltd. | Asymmetric auxiliary group |
| CN102875558A (zh) * | 2012-11-05 | 2013-01-16 | 贵州大学 | 2-氯-4-取代-8-硝基苯并呋喃[3,2-d]嘧啶类化合物及其制备方法和用途 |
| CN103044370A (zh) * | 2012-12-28 | 2013-04-17 | 山东邹平大展新材料有限公司 | 一种5-(哌嗪-1-基)苯并呋喃-2-甲酰胺的制备方法 |
| CN104045642B (zh) * | 2013-03-14 | 2016-08-24 | 上海医药工业研究院 | 含嘧啶或吡啶的稠环化合物及其作为抗肿瘤药物的应用 |
| JPWO2015108048A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤 |
| JPWO2015108046A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗アレルギー作用を有するキラル核酸アジュバンド及び抗アレルギー剤 |
| WO2015108047A1 (ja) | 2014-01-15 | 2015-07-23 | 株式会社新日本科学 | 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤 |
| KR20230152178A (ko) | 2014-01-16 | 2023-11-02 | 웨이브 라이프 사이언시스 리미티드 | 키랄 디자인 |
| WO2015115355A1 (ja) | 2014-01-31 | 2015-08-06 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
| CN106255679B (zh) * | 2014-02-27 | 2019-09-06 | 默克专利有限公司 | 用作nav通道抑制剂的杂环化合物及其用途 |
| WO2015152319A1 (ja) * | 2014-04-02 | 2015-10-08 | 株式会社 三和化学研究所 | 5,7-無置換-ピラゾロ[1,5-a]ピリミジン-6-カルボン酸の製造方法 |
| KR101837565B1 (ko) | 2014-08-06 | 2018-03-12 | 삼성에스디아이 주식회사 | 유기 화합물, 유기 광전자 소자 및 표시 장치 |
| JP6840931B2 (ja) * | 2015-03-09 | 2021-03-10 | 東ソー株式会社 | 縮環芳香族化合物の製造方法 |
| EP3538523B1 (en) | 2016-11-08 | 2021-05-19 | Cancer Research Technology Limited | Pyrimidinone derivatives as cdc7 inhibitors |
| NL2021185B1 (en) | 2018-06-26 | 2020-01-06 | Stichting Het Nederlands Kanker Inst Antoni Van Leeuwenhoek Ziekenhuis | Combination Therapy and Use Thereof for Treating Cancer |
| WO2020068729A1 (en) | 2018-09-25 | 2020-04-02 | Incyte Corporation | Pyrazolo[4,3-d]pyrimidine compounds as alk2 abd/or fgfr modulators |
| CN111689947B (zh) * | 2019-03-13 | 2023-07-14 | 鲁南制药集团股份有限公司 | 替加氟-l-脯氨酸共晶体及其制备方法 |
| CA3164707A1 (en) * | 2020-02-03 | 2021-08-12 | Ana Maria Garcia Collazo | Combination therapy for treating mps1 |
| WO2021198191A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| IL301866A (en) * | 2020-10-05 | 2023-06-01 | Japan Tobacco Inc | Tetrahydrobenzofurodiazepinone compounds and their remote applications |
| WO2022194799A1 (de) | 2021-03-18 | 2022-09-22 | Merck Patent Gmbh | Heteroaromatische verbindungen für organische elektrolumineszenzvorrichtungen |
| KR20240149429A (ko) * | 2022-02-16 | 2024-10-14 | 듀크 스트리트 바이오 리미티드 | 약학적 화합물 |
| CN116731025B (zh) * | 2023-05-24 | 2025-06-24 | 曲阜师范大学 | 一种具有2-芳基苯并呋喃并[2,3-d]嘧啶酮类结构的荧光材料及其制备方法和应用 |
| CN120114459B (zh) * | 2025-05-14 | 2025-07-29 | 南京工业大学 | 苯并呋喃嘧啶酮或苯并噻吩嘧啶酮类化合物的应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL112248A0 (en) * | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| WO2002051849A1 (en) | 2000-12-26 | 2002-07-04 | Daiichi Pharmaceutical Co., Ltd. | Cdk4 inhibitors |
| CA2444598A1 (en) * | 2001-04-20 | 2003-10-31 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of gsk-3 |
| US7345046B2 (en) * | 2003-05-30 | 2008-03-18 | Chiron Corporation | Heteroaryl-fused pyrimidinyl compounds as anticancer agents |
| WO2006023381A1 (en) * | 2004-08-16 | 2006-03-02 | Taigen Biotechnology | Pyrimidinone compounds |
| AU2005303893A1 (en) * | 2004-11-11 | 2006-05-18 | Argenta Discovery Ltd | Pyrimidine compounds as histamine modulators |
| EP1776982A1 (en) | 2005-10-18 | 2007-04-25 | Argenta Discovery Limited | Pyrimidine compounds as histamine modulators |
-
2008
- 2008-12-19 TW TW097149655A patent/TW200930375A/zh unknown
- 2008-12-19 AR ARP080105615A patent/AR069869A1/es unknown
- 2008-12-19 PE PE2008002147A patent/PE20091669A1/es not_active Application Discontinuation
- 2008-12-22 EA EA201070786A patent/EA019785B1/ru not_active IP Right Cessation
- 2008-12-22 NZ NZ586936A patent/NZ586936A/en not_active IP Right Cessation
- 2008-12-22 CN CN2008801272275A patent/CN101965351A/zh active Pending
- 2008-12-22 MX MX2010006799A patent/MX2010006799A/es active IP Right Grant
- 2008-12-22 EP EP08832770A patent/EP2097419B1/en active Active
- 2008-12-22 WO PCT/US2008/087939 patent/WO2009086264A1/en not_active Ceased
- 2008-12-22 JP JP2010539930A patent/JP2011507908A/ja not_active Ceased
- 2008-12-22 KR KR1020107016179A patent/KR20100098714A/ko not_active Ceased
- 2008-12-22 CA CA2712358A patent/CA2712358A1/en not_active Abandoned
- 2008-12-22 AU AU2008345560A patent/AU2008345560A1/en not_active Abandoned
- 2008-12-22 AT AT08832770T patent/ATE510839T1/de not_active IP Right Cessation
- 2008-12-22 US US12/341,210 patent/US20090247559A1/en not_active Abandoned
- 2008-12-22 CL CL2008003873A patent/CL2008003873A1/es unknown
- 2008-12-22 BR BRPI0821573A patent/BRPI0821573A2/pt not_active IP Right Cessation
-
2010
- 2010-06-15 ZA ZA2010/04243A patent/ZA201004243B/en unknown
- 2010-06-16 IL IL206416A patent/IL206416A0/en unknown
- 2010-07-21 CO CO10088575A patent/CO6321258A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| IL206416A0 (en) | 2010-12-30 |
| EA201070786A1 (ru) | 2011-02-28 |
| BRPI0821573A2 (pt) | 2016-08-09 |
| TW200930375A (en) | 2009-07-16 |
| US20090247559A1 (en) | 2009-10-01 |
| KR20100098714A (ko) | 2010-09-08 |
| WO2009086264A1 (en) | 2009-07-09 |
| AU2008345560A1 (en) | 2009-07-09 |
| ATE510839T1 (de) | 2011-06-15 |
| JP2011507908A (ja) | 2011-03-10 |
| CL2008003873A1 (es) | 2009-06-26 |
| ZA201004243B (en) | 2011-03-30 |
| EA019785B1 (ru) | 2014-06-30 |
| AR069869A1 (es) | 2010-02-24 |
| CN101965351A (zh) | 2011-02-02 |
| EP2097419B1 (en) | 2011-05-25 |
| NZ586936A (en) | 2012-07-27 |
| CO6321258A2 (es) | 2011-09-20 |
| MX2010006799A (es) | 2010-10-05 |
| EP2097419A1 (en) | 2009-09-09 |
| CA2712358A1 (en) | 2009-07-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |