MA47409A - Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanes - Google Patents
Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanesInfo
- Publication number
- MA47409A MA47409A MA047409A MA47409A MA47409A MA 47409 A MA47409 A MA 47409A MA 047409 A MA047409 A MA 047409A MA 47409 A MA47409 A MA 47409A MA 47409 A MA47409 A MA 47409A
- Authority
- MA
- Morocco
- Prior art keywords
- trifluoromethylcyclopropanes
- aryl
- synthesis
- new process
- new
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/377—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
- C07C51/38—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups by decarboxylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/08—Preparation of carboxylic acids or their salts, halides or anhydrides from nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/363—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/58—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/62—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings and other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/65—Halogen-containing esters of unsaturated acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17154826 | 2017-02-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA47409A true MA47409A (fr) | 2019-12-11 |
Family
ID=57965840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA047409A MA47409A (fr) | 2017-02-06 | 2018-02-05 | Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanes |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US10899695B2 (fr) |
| EP (1) | EP3577099B1 (fr) |
| JP (1) | JP6972144B2 (fr) |
| KR (1) | KR102608490B1 (fr) |
| CN (1) | CN110234622B (fr) |
| CA (1) | CA3050348A1 (fr) |
| ES (1) | ES2971626T3 (fr) |
| IL (1) | IL268456B (fr) |
| MA (1) | MA47409A (fr) |
| MX (1) | MX2019009242A (fr) |
| TW (1) | TWI808960B (fr) |
| WO (1) | WO2018141961A1 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI808952B (zh) | 2016-12-16 | 2023-07-21 | 瑞士商愛杜西亞製藥有限公司 | 包含t型鈣通道阻斷劑之醫藥組合 |
| WO2019008034A1 (fr) | 2017-07-05 | 2019-01-10 | Idorsia Pharmaceuticals Ltd | Forme cristalline de n-[1-(5-cyano-pyridin-2-ylméthyl)-1h-pyrazol-3-yl]-2-[4-(1-trifluorométhyl-cyclopropyl)-phényl]-acétamide |
| WO2023240205A1 (fr) | 2022-06-10 | 2023-12-14 | Neurocrine Biosciences, Inc. | Composés deutérés |
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| WO2002000651A2 (fr) | 2000-06-27 | 2002-01-03 | Bristol-Myers Squibb Pharma Company | Inhibiteurs du facteur xa |
| EP1359911A2 (fr) | 2000-12-29 | 2003-11-12 | Alteon, Inc. | Procede de traitement de troubles fibrogenes et autres symptomes de type ivc |
| EP1353674A1 (fr) | 2000-12-29 | 2003-10-22 | Alteon, Inc. | Methode de traitement du glaucome ivb |
| ES2338539T3 (es) | 2001-11-01 | 2010-05-10 | Icagen, Inc. | Pirazolamidas para uso en el tratamiento del dolor. |
| US7105548B2 (en) | 2001-12-18 | 2006-09-12 | Merck & Co., Inc. | Heteroaryl substituted triazole modulators of metabotropic glutamate receptor-5 |
| US7569592B2 (en) | 2001-12-18 | 2009-08-04 | Merck & Co., Inc. | Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5 |
| SE0201658D0 (sv) | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | Immediate release pharmaceutical formulation |
| CN100387594C (zh) | 2003-04-03 | 2008-05-14 | 麦克公司 | 二芳基取代的吡唑类代谢型谷氨酸受体-5调节剂 |
| US7268151B2 (en) | 2003-04-04 | 2007-09-11 | Merck & Co., Inc. | Di-aryl substituted triazole modulators of metabotropic glutamate receptor-5 |
| US20040220170A1 (en) | 2003-05-01 | 2004-11-04 | Atkinson Robert N. | Pyrazole-amides and sulfonamides as sodium channel modulators |
| GB0328796D0 (en) | 2003-12-12 | 2004-01-14 | Biofocus Plc | Compounds which interact with the G-protein coupled receptor family |
| GEP20094751B (en) | 2004-08-18 | 2009-08-10 | Pfizer | Inhibitors of hepatitis c virus rna-dependent rna polymerase, and compositions and treatments using the same |
| ES2321535T3 (es) | 2004-12-23 | 2009-06-08 | Glaxo Group Limited | Compuestos de piridina para el tratamiento de enfermedades mediadas por prostaglandinas. |
| GB0508463D0 (en) | 2005-04-26 | 2005-06-01 | Glaxo Group Ltd | Compounds |
| GB0508472D0 (en) | 2005-04-26 | 2005-06-01 | Glaxo Group Ltd | Compounds |
| AU2006327173A1 (en) | 2005-12-22 | 2007-06-28 | Icagen, Inc. | Calcium channel antagonists |
| MX2008013238A (es) | 2006-04-12 | 2008-10-21 | Merck & Co Inc | Antagonistas de los canales de calcio de tipo t de piridil amida. |
| KR20090025358A (ko) | 2006-07-24 | 2009-03-10 | 에프. 호프만-라 로슈 아게 | 글루코키나제 활성화제로서의 피라졸 |
| US7902248B2 (en) | 2006-12-14 | 2011-03-08 | Hoffmann-La Roche Inc. | Oxime glucokinase activators |
| WO2008085888A1 (fr) | 2007-01-05 | 2008-07-17 | Arena Pharmaceuticals, Inc. | Récepteur couplé aux protéines g et modulateur dudit récepteur pour le traitement de troubles neurologiques liés au gaba et notamment de troubles liés au sommeil |
| WO2008156726A1 (fr) | 2007-06-20 | 2008-12-24 | Merck & Co., Inc. | Inhibiteurs des janus kinases |
| AU2008310519B2 (en) | 2007-10-08 | 2013-05-02 | Advinus Therapeutics Private Limited | Acetamide derivatives as glucokinase activators, their process and medicinal applications |
| JP5524071B2 (ja) | 2007-10-24 | 2014-06-18 | メルク・シャープ・アンド・ドーム・コーポレーション | 複素環フェニルアミドｔ型カルシウムチャネルアンタゴニスト |
| CA2703471A1 (fr) | 2007-10-24 | 2009-04-30 | Merck Sharp & Dohme Corp. | Antagonistes des canaux calciques de type t a base d'amide de pyrazinyle |
| EP2212293A4 (fr) | 2007-10-24 | 2010-12-01 | Merck Sharp & Dohme | Antagonistes des canaux calciques de type t à base d'amide hétérocyclique |
| WO2009118596A2 (fr) | 2008-03-26 | 2009-10-01 | Glenmark Pharmaceuticals, S. A. | Dérivés de phtalimide en tant que modulateurs de trpa1 |
| JP2011516442A (ja) | 2008-04-04 | 2011-05-26 | ビオマリン アイジーエー リミテッド | 筋ジストロフィーを治療するための化合物 |
| US7951814B2 (en) | 2008-06-17 | 2011-05-31 | Glenmark Pharmaceuticals, S.A. | Quinazolinedione derivatives as TRPA1 modulators |
| BRPI0921257A2 (pt) | 2008-11-14 | 2016-02-23 | Bayer Schering Pharma Ag | composto de arila heterociclicamente subsittuidos como inibidores hif |
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| WO2010075376A2 (fr) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Composés antiviraux |
| US20100273744A1 (en) | 2009-04-24 | 2010-10-28 | Paul Martin Gore | Compounds |
| MX2011012943A (es) | 2009-06-04 | 2012-01-27 | Novartis Ag | Derivados de 1h-imidazo-[4,5-c]-quinolinona. |
| WO2011022315A1 (fr) | 2009-08-19 | 2011-02-24 | Merck Sharp & Dohme Corp. | Antagonistes de canal calcium de type t de pyrazinylphénylamide |
| US8993612B2 (en) | 2009-10-08 | 2015-03-31 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
| WO2011053542A1 (fr) | 2009-10-30 | 2011-05-05 | Merck Sharp & Dohme Corp. | Antagonistes des canaux calciques de type t amides hétérocycliques |
| CA2782885A1 (fr) | 2009-12-21 | 2011-07-14 | Merck Sharp & Dohme Corp. | Inhibiteurs de tyrosine kinase |
| JPWO2011093352A1 (ja) | 2010-01-27 | 2013-06-06 | 武田薬品工業株式会社 | チアゾール誘導体 |
| EP2402327B1 (fr) | 2010-06-29 | 2018-03-07 | Impetis Biosciences Ltd. | Composés d'acétamide en tant qu'activateurs de la glucokinase, leur procédé et applications médicales |
| US8580829B2 (en) | 2010-08-26 | 2013-11-12 | Boehringer Ingelheim International Gmbh | Oxadiazole inhibitors of leukotriene production |
| KR20120063283A (ko) | 2010-12-07 | 2012-06-15 | 제일약품주식회사 | 신규한 피라졸로 피리딘 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 포함하는 약학적 조성물 |
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| KR101685993B1 (ko) | 2014-05-15 | 2016-12-13 | 한국과학기술연구원 | 전압개폐 칼슘이온채널 억제 활성화능을 갖는 ｎ-(피라졸릴메틸)아릴설폰아마이드 화합물 및 이를 포함하는 약학적 조성물 |
| HUE040489T2 (hu) | 2014-06-03 | 2019-03-28 | Idorsia Pharmaceuticals Ltd | Pirazolvegyületek és alkalmazásuk t-típusú kalciumcsatorna-blokkolókként |
| AU2015317022B2 (en) | 2014-09-15 | 2020-01-16 | Idorsia Pharmaceuticals Ltd | Triazole compounds as T-type calcium channel blockers |
| AU2016211292B2 (en) | 2015-01-30 | 2020-05-07 | Neurocrine Biosciences, Inc. | Substituted triazoles and methods relating thereto |
| TWI808952B (zh) | 2016-12-16 | 2023-07-21 | 瑞士商愛杜西亞製藥有限公司 | 包含t型鈣通道阻斷劑之醫藥組合 |
| WO2019008034A1 (fr) | 2017-07-05 | 2019-01-10 | Idorsia Pharmaceuticals Ltd | Forme cristalline de n-[1-(5-cyano-pyridin-2-ylméthyl)-1h-pyrazol-3-yl]-2-[4-(1-trifluorométhyl-cyclopropyl)-phényl]-acétamide |
-
2018
- 2018-02-05 MA MA047409A patent/MA47409A/fr unknown
- 2018-02-05 WO PCT/EP2018/052808 patent/WO2018141961A1/fr active Application Filing
- 2018-02-05 EP EP18702308.0A patent/EP3577099B1/fr active Active
- 2018-02-05 JP JP2019542367A patent/JP6972144B2/ja active Active
- 2018-02-05 CN CN201880009897.0A patent/CN110234622B/zh active Active
- 2018-02-05 CA CA3050348A patent/CA3050348A1/fr active Pending
- 2018-02-05 ES ES18702308T patent/ES2971626T3/es active Active
- 2018-02-05 TW TW107103934A patent/TWI808960B/zh active
- 2018-02-05 KR KR1020197025869A patent/KR102608490B1/ko active IP Right Grant
- 2018-02-05 MX MX2019009242A patent/MX2019009242A/es active IP Right Grant
- 2018-02-05 US US16/483,247 patent/US10899695B2/en active Active
-
2019
- 2019-08-04 IL IL268456A patent/IL268456B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR102608490B1 (ko) | 2023-11-30 |
| WO2018141961A1 (fr) | 2018-08-09 |
| JP2020506939A (ja) | 2020-03-05 |
| EP3577099A1 (fr) | 2019-12-11 |
| US10899695B2 (en) | 2021-01-26 |
| EP3577099C0 (fr) | 2024-01-24 |
| ES2971626T3 (es) | 2024-06-06 |
| IL268456B (en) | 2021-07-29 |
| TW201833069A (zh) | 2018-09-16 |
| EP3577099B1 (fr) | 2024-01-24 |
| IL268456A (en) | 2019-09-26 |
| CN110234622B (zh) | 2023-07-04 |
| CA3050348A1 (fr) | 2018-08-09 |
| US20190375702A1 (en) | 2019-12-12 |
| CN110234622A (zh) | 2019-09-13 |
| KR20190116350A (ko) | 2019-10-14 |
| MX2019009242A (es) | 2019-09-13 |
| TWI808960B (zh) | 2023-07-21 |
| JP6972144B2 (ja) | 2021-11-24 |
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