PT2872501T - Derivados de pirazolil pirimidina - Google Patents
Derivados de pirazolil pirimidinaInfo
- Publication number
- PT2872501T PT2872501T PT137371340T PT13737134T PT2872501T PT 2872501 T PT2872501 T PT 2872501T PT 137371340 T PT137371340 T PT 137371340T PT 13737134 T PT13737134 T PT 13737134T PT 2872501 T PT2872501 T PT 2872501T
- Authority
- PT
- Portugal
- Prior art keywords
- pyrazolyl derivatives
- pyrimidine
- pyrimidine pyrazolyl
- derivatives
- pyrazolyl
- Prior art date
Links
Classifications
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- 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
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- 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
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- 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
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261669843P | 2012-07-10 | 2012-07-10 | |
EP12175660 | 2012-07-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
PT2872501T true PT2872501T (pt) | 2016-09-06 |
Family
ID=49915426
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PT137371340T PT2872501T (pt) | 2012-07-10 | 2013-07-03 | Derivados de pirazolil pirimidina |
Country Status (19)
Country | Link |
---|---|
US (1) | US9216991B2 (pt) |
EP (1) | EP2872501B1 (pt) |
JP (1) | JP6189434B2 (pt) |
KR (1) | KR20150033716A (pt) |
CN (1) | CN104662014B (pt) |
AU (1) | AU2013289615B2 (pt) |
BR (1) | BR112015000399A2 (pt) |
CA (1) | CA2878621C (pt) |
DK (1) | DK2872501T3 (pt) |
ES (1) | ES2589558T3 (pt) |
HK (1) | HK1210778A1 (pt) |
HU (1) | HUE029559T2 (pt) |
IL (1) | IL236542B (pt) |
MX (1) | MX2015000129A (pt) |
PT (1) | PT2872501T (pt) |
RU (1) | RU2015104123A (pt) |
SG (1) | SG11201500005SA (pt) |
WO (1) | WO2014008992A1 (pt) |
ZA (1) | ZA201500917B (pt) |
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CA2933107C (en) * | 2014-01-09 | 2022-06-21 | Merck Patent Gmbh | Pyrimidine pyrazolyl derivatives and their use as irak inhibitors |
PL3129023T3 (pl) * | 2014-03-27 | 2021-08-16 | Eicosis, Llc | Silne inhibitory rozpuszczalnej hydrolazy epoksydowej |
ES2772133T3 (es) | 2014-11-20 | 2020-07-07 | Merck Patent Gmbh | Compuestos heteroarilo como inhibidores de IRAK y sus usos |
CN105153211B (zh) * | 2015-09-22 | 2017-02-01 | 上海晋鲁医药科技有限公司 | 一种合成1‑(N‑Boc‑4‑哌啶)‑4‑吡唑硼酸频哪醇酯的方法 |
JP6947743B2 (ja) | 2016-03-03 | 2021-10-13 | バイエル・ファルマ・アクティエンゲゼルシャフト | 新規な2−置換インダゾール、その製造方法、それを含有する医薬製剤、および薬物を製造するためのその使用 |
JOP20180011A1 (ar) | 2017-02-16 | 2019-01-30 | Gilead Sciences Inc | مشتقات بيرولو [1، 2-b]بيريدازين |
MX2019010642A (es) | 2017-03-16 | 2019-10-17 | Celgene Car Llc | Inhibidores de cinasa activada por mitogeno 2 (mk2), sintesis de los mismos, e intermediarios de los mismos. |
CN106967073A (zh) * | 2017-04-24 | 2017-07-21 | 刘双伟 | 一种治疗类风湿性关节炎的药物 |
CN106946891B (zh) * | 2017-05-08 | 2018-07-13 | 宿州市徽腾知识产权咨询有限公司 | 一种用于治疗类风湿性关节炎的药物 |
IL273432B (en) | 2017-09-22 | 2022-09-01 | Kymera Therapeutics Inc | Protein compounds and their uses |
WO2019060693A1 (en) | 2017-09-22 | 2019-03-28 | Kymera Therapeutics, Inc. | CRBN LIGANDS AND USES THEREOF |
WO2019111218A1 (en) | 2017-12-08 | 2019-06-13 | Cadila Healthcare Limited | Novel heterocyclic compounds as irak4 inhibitors |
US10874743B2 (en) | 2017-12-26 | 2020-12-29 | Kymera Therapeutics, Inc. | IRAK degraders and uses thereof |
US11485743B2 (en) | 2018-01-12 | 2022-11-01 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
US11512080B2 (en) | 2018-01-12 | 2022-11-29 | Kymera Therapeutics, Inc. | CRBN ligands and uses thereof |
US11292792B2 (en) | 2018-07-06 | 2022-04-05 | Kymera Therapeutics, Inc. | Tricyclic CRBN ligands and uses thereof |
TWI721483B (zh) | 2018-07-13 | 2021-03-11 | 美商基利科學股份有限公司 | 吡咯并[1,2-b]嗒𠯤衍生物 |
JP7186874B2 (ja) * | 2018-10-26 | 2022-12-09 | アーリーン ファーマシューティカルズ エルエルシー | ピラゾリル化合物およびその使用方法 |
JP2022516401A (ja) | 2018-11-30 | 2022-02-28 | カイメラ セラピューティクス, インコーポレイテッド | Irak分解剤およびそれらの使用 |
WO2021099406A1 (en) * | 2019-11-20 | 2021-05-27 | F. Hoffmann-La Roche Ag | Spiro(isobenzofuranazetidine) compounds for the treatment of autoimmune disease |
CN110950839B (zh) * | 2019-12-17 | 2023-04-14 | 蚌埠中实化学技术有限公司 | 4-(4-卤代-1h-吡唑-1-基)哌啶-1-羧酸叔丁酯的制备方法 |
TW202136251A (zh) | 2019-12-17 | 2021-10-01 | 美商凱麥拉醫療公司 | Irak降解劑及其用途 |
US11591332B2 (en) | 2019-12-17 | 2023-02-28 | Kymera Therapeutics, Inc. | IRAK degraders and uses thereof |
TW202210483A (zh) | 2020-06-03 | 2022-03-16 | 美商凱麥拉醫療公司 | Irak降解劑之結晶型 |
AR124726A1 (es) * | 2021-02-01 | 2023-04-26 | Celgene Corp | Inhibidores de nk2, su síntesis y sus intermedios |
WO2024011116A2 (en) * | 2022-07-07 | 2024-01-11 | Dana-Farber Cancer Institute, Inc. | Potent and selective irreversible inhibitors of irak1 |
CN115490621B (zh) * | 2022-10-14 | 2024-06-21 | 浙江工业大学 | 一种碘代双环[1.1.1]戊烷衍生物的制备方法 |
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US5559137A (en) * | 1994-05-16 | 1996-09-24 | Smithkline Beecham Corp. | Compounds |
EP1345922B1 (en) * | 2000-12-21 | 2006-05-31 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
US7659270B2 (en) * | 2006-08-11 | 2010-02-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
DE102008025750A1 (de) * | 2008-05-29 | 2009-12-03 | Merck Patent Gmbh | Dihydropyrazolderivate |
DE102008062825A1 (de) * | 2008-12-23 | 2010-06-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo [4,3-b]pyridazin-derivate |
WO2010100144A1 (en) | 2009-03-04 | 2010-09-10 | Merck Serono S.A. | Fused bicyclic compounds as inhibitors for pi3 kinase |
EP2414337B1 (en) * | 2009-04-03 | 2013-05-01 | Cellzome GmbH | Methods for the identification of kinase interacting molecules and for the purification of kinase proteins |
DE102009033208A1 (de) * | 2009-07-15 | 2011-01-20 | Merck Patent Gmbh | Aminopyridinderivate |
CA2782885A1 (en) * | 2009-12-21 | 2011-07-14 | Merck Sharp & Dohme Corp. | Tyrosine kinase inhibitors |
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 |
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- 2013-07-03 JP JP2015520844A patent/JP6189434B2/ja active Active
- 2013-07-03 KR KR20157003049A patent/KR20150033716A/ko not_active Application Discontinuation
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Publication number | Publication date |
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CN104662014A (zh) | 2015-05-27 |
RU2015104123A (ru) | 2016-08-27 |
CN104662014B (zh) | 2017-02-22 |
CA2878621C (en) | 2020-09-15 |
MX2015000129A (es) | 2015-04-14 |
EP2872501B1 (en) | 2016-06-01 |
JP6189434B2 (ja) | 2017-08-30 |
HK1210778A1 (en) | 2016-05-06 |
IL236542A0 (en) | 2015-02-26 |
AU2013289615A1 (en) | 2015-02-26 |
HUE029559T2 (en) | 2017-03-28 |
US9216991B2 (en) | 2015-12-22 |
SG11201500005SA (en) | 2015-01-29 |
IL236542B (en) | 2018-05-31 |
AU2013289615B2 (en) | 2017-06-08 |
CA2878621A1 (en) | 2014-01-16 |
KR20150033716A (ko) | 2015-04-01 |
WO2014008992A1 (en) | 2014-01-16 |
EP2872501A1 (en) | 2015-05-20 |
DK2872501T3 (en) | 2016-08-29 |
ZA201500917B (en) | 2017-08-30 |
JP2015522045A (ja) | 2015-08-03 |
US20150141396A1 (en) | 2015-05-21 |
ES2589558T3 (es) | 2016-11-15 |
BR112015000399A2 (pt) | 2017-06-27 |
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