MA47409A - Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanes - Google Patents

Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanes

Info

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
Application number
MA047409A
Other languages
English (en)
Inventor
Stefan Abele
Lee Mclaren
Daniel To
David Tovell
Original Assignee
Idorsia Pharmaceuticals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Idorsia Pharmaceuticals Ltd filed Critical Idorsia Pharmaceuticals Ltd
Publication of MA47409A publication Critical patent/MA47409A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation 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
    • C07C67/343Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/377Preparation 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
    • C07C51/38Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/08Preparation of carboxylic acids or their salts, halides or anhydrides from nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/363Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/52Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
    • C07C57/58Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/52Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
    • C07C57/62Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings and other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/09Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/62Halogen-containing esters
    • C07C69/65Halogen-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)
MA047409A 2017-02-06 2018-02-05 Nouveau procédé de synthèse de 1-aryl-1-trifluorométhylcyclopropanes MA47409A (fr)

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) MX376203B (fr)
TW (1) TWI808960B (fr)
WO (1) WO2018141961A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3554490B1 (fr) 2016-12-16 2022-02-16 Idorsia Pharmaceuticals Ltd Combinaison pharmaceutique comprenant un bloqueur de canal calcique de type t
MY206357A (en) 2017-07-05 2024-12-12 Idorsia Pharmaceuticals Ltd Crystalline form of n -[1-(5-cyano-pyridin-2-ylmethyl)-1 h -pyrazol-3-yl]-2-[4-(1-trifluoromethyl-cyclopropyl)-phenyl]-acetamide
WO2023240205A1 (fr) 2022-06-10 2023-12-14 Neurocrine Biosciences, Inc. Composés deutérés

Family Cites Families (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69526790T2 (de) 1994-06-24 2003-03-06 Euroceltique S.A., Luxemburg/Luxembourg Verbindungen zur hemmung von phosphodiesrerase iv
AU730224B2 (en) 1996-12-23 2001-03-01 Du Pont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
AU2001273040A1 (en) 2000-06-27 2002-01-08 Du Pont Pharmaceuticals Company Factor xa inhibitors
WO2002053160A1 (fr) 2000-12-29 2002-07-11 Alteon, Inc. Methode de traitement du glaucome ivb
EP1359911A2 (fr) 2000-12-29 2003-11-12 Alteon, Inc. Procede de traitement de troubles fibrogenes et autres symptomes de type ivc
DE60235114D1 (de) 2001-11-01 2010-03-04 Icagen Inc Pyrazolamide zur anwendung in der behandlung von schmerz
JP4286146B2 (ja) 2001-12-18 2009-06-24 メルク エンド カムパニー インコーポレーテッド メタボトロピックグルタミン酸受容体−5のヘテロアリール置換ピラゾール系調節剤
US7105548B2 (en) 2001-12-18 2006-09-12 Merck & Co., Inc. Heteroaryl substituted triazole modulators of metabotropic glutamate receptor-5
SE0201658D0 (sv) 2002-05-31 2002-05-31 Astrazeneca Ab Immediate release pharmaceutical formulation
AU2004228057A1 (en) 2003-04-03 2004-10-21 Merck & Co., Inc. Di-aryl substituted pyrazole modulators of metabotropic glutamate receptor-5
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
AP2313A (en) 2004-08-18 2011-10-31 Pfizer Inhibitors of hepatitis C virus RNA-dependent RNA ploymerase, and compositions and treatments using the same.
EP1833795B1 (fr) 2004-12-23 2009-03-04 Glaxo Group Limited Composes de pyridine destines au traitement de maladies a mediation par prostaglandine
GB0508463D0 (en) 2005-04-26 2005-06-01 Glaxo Group Ltd Compounds
GB0508472D0 (en) 2005-04-26 2005-06-01 Glaxo Group Ltd Compounds
US20070197523A1 (en) 2005-12-22 2007-08-23 Icagen, Inc. Calcium channel antagonists
KR20080108539A (ko) 2006-04-12 2008-12-15 머크 앤드 캄파니 인코포레이티드 피리딜 아미드 t-형 칼슘 채널 길항제
CA2657566A1 (fr) 2006-07-24 2008-01-31 F. Hoffmann-La Roche Ag Pyrazoles comme activateurs de glucokinase
US7902248B2 (en) 2006-12-14 2011-03-08 Hoffmann-La Roche Inc. Oxime glucokinase activators
US20110038850A1 (en) 2007-01-05 2011-02-17 Didier Bagnol G Protein-Coupled Receptor and Modulators Thereof For The Treatment of Gaba-Related Neurological Disorders Including Sleep-Related Disorders
US8367706B2 (en) 2007-06-20 2013-02-05 Merck Sharp & Dohme Corp. Inhibitors of janus kinases
CA2700783C (fr) 2007-10-08 2015-03-17 Advinus Therapeutics Private Limited Derives acetamide comme activateur de la glucokinase, leur procede et applications medicinales
JP2011500808A (ja) 2007-10-24 2011-01-06 メルク・シャープ・エンド・ドーム・コーポレイション 複素環アミドt型カルシウムチャネルアンタゴニスト
WO2009054982A1 (fr) 2007-10-24 2009-04-30 Merck & Co., Inc. Antagonistes des canaux calciques de type t à base d'amide de pyrazinyle
WO2009054984A1 (fr) 2007-10-24 2009-04-30 Merck & Co., Inc. Antagonistes de canaux calciques de type t à base de phényle amide hétérocyclique
WO2009118596A2 (fr) 2008-03-26 2009-10-01 Glenmark Pharmaceuticals, S. A. Dérivés de phtalimide en tant que modulateurs de trpa1
AU2009231258A1 (en) 2008-04-04 2009-10-08 Biomarin Iga Limited Compounds for treating muscular dystrophy
WO2010004390A1 (fr) 2008-06-17 2010-01-14 Glenmark Pharmaceuticals, S.A. Dérivés de quinazoline dione en tant que modulateurs de trpa1
PL2356113T3 (pl) 2008-11-14 2015-06-30 Bayer Ip Gmbh Heterocyklicznie podstawione związki arylowe jako inhibitory HIF
WO2010073011A2 (fr) 2008-12-23 2010-07-01 Betagenon Ab Composés utiles comme médicaments
CN102264737A (zh) 2008-12-23 2011-11-30 雅培制药有限公司 抗病毒化合物
US20100273744A1 (en) 2009-04-24 2010-10-28 Paul Martin Gore Compounds
CN102574845B (zh) 2009-06-04 2015-09-02 诺华股份有限公司 1H-咪唑并[4,5-c]喹啉酮衍生物
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
EP2493297B1 (fr) 2009-10-30 2016-08-17 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
WO2011093352A1 (fr) 2010-01-27 2011-08-04 武田薬品工業株式会社 Dérivé de thiazole
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
EA024782B1 (ru) 2011-03-07 2016-10-31 Пфайзер Инк. Производные фторпиридинона, полезные в качестве антибактериальных агентов
US8759380B2 (en) 2011-04-22 2014-06-24 Cytokinetics, Inc. Certain heterocycles, compositions thereof, and methods for their use
UY34200A (es) 2011-07-21 2013-02-28 Bayer Ip Gmbh 3-(fluorovinil)pirazoles y su uso
US9006235B2 (en) 2012-03-06 2015-04-14 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
WO2014125408A2 (fr) * 2013-02-12 2014-08-21 Aurigene Discovery Technologies Limited Dérivés de 1h-pyrrolopyridinone substitués en tant qu'inhibiteurs de kinase
EP2991994B1 (fr) 2013-05-01 2018-08-15 Vitae Pharmaceuticals, Inc. Inhibiteurs du ror-gamma à base de thiazolopyrrolidine
AR096393A1 (es) 2013-05-23 2015-12-30 Bayer Cropscience Ag Compuestos heterocíclicos pesticidas
EP3031265B1 (fr) * 2013-08-08 2017-12-06 Sony Corporation Réseau de communication mobile, dispositif de communication et procédés
KR101685993B1 (ko) 2014-05-15 2016-12-13 한국과학기술연구원 전압개폐 칼슘이온채널 억제 활성화능을 갖는 n-(피라졸릴메틸)아릴설폰아마이드 화합물 및 이를 포함하는 약학적 조성물
DK3152199T3 (en) * 2014-06-03 2018-11-26 Idorsia Pharmaceuticals Ltd PYRAZOLE COMPOUNDS AND THEIR USE AS T-TYPE CALCIUM CHANNEL BLOCKERS
CN107074822B (zh) 2014-09-15 2020-01-03 爱杜西亚药品有限公司 作为t型钙通道阻断剂的三唑化合物
PL3250563T3 (pl) 2015-01-30 2022-05-02 Neurocrine Biosciences, Inc. Podstawione triazole i dotyczące ich sposoby
EP3554490B1 (fr) 2016-12-16 2022-02-16 Idorsia Pharmaceuticals Ltd Combinaison pharmaceutique comprenant un bloqueur de canal calcique de type t
MY206357A (en) 2017-07-05 2024-12-12 Idorsia Pharmaceuticals Ltd Crystalline form of n -[1-(5-cyano-pyridin-2-ylmethyl)-1 h -pyrazol-3-yl]-2-[4-(1-trifluoromethyl-cyclopropyl)-phenyl]-acetamide

Also Published As

Publication number Publication date
JP6972144B2 (ja) 2021-11-24
KR20190116350A (ko) 2019-10-14
TW201833069A (zh) 2018-09-16
KR102608490B1 (ko) 2023-11-30
EP3577099B1 (fr) 2024-01-24
US20190375702A1 (en) 2019-12-12
US10899695B2 (en) 2021-01-26
MX2019009242A (es) 2019-09-13
TWI808960B (zh) 2023-07-21
JP2020506939A (ja) 2020-03-05
WO2018141961A1 (fr) 2018-08-09
IL268456A (en) 2019-09-26
EP3577099A1 (fr) 2019-12-11
CN110234622A (zh) 2019-09-13
MX376203B (es) 2025-03-07
ES2971626T3 (es) 2024-06-06
CA3050348A1 (fr) 2018-08-09
EP3577099C0 (fr) 2024-01-24
CN110234622B (zh) 2023-07-04
IL268456B (en) 2021-07-29

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