JP2015516945A5 - - Google Patents

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Publication number
JP2015516945A5
JP2015516945A5 JP2015500539A JP2015500539A JP2015516945A5 JP 2015516945 A5 JP2015516945 A5 JP 2015516945A5 JP 2015500539 A JP2015500539 A JP 2015500539A JP 2015500539 A JP2015500539 A JP 2015500539A JP 2015516945 A5 JP2015516945 A5 JP 2015516945A5
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JP
Japan
Prior art keywords
bis
quaternary alkaloid
methoxy
vinyl
salt according
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.)
Granted
Application number
JP2015500539A
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English (en)
Japanese (ja)
Other versions
JP6140266B2 (ja
JP2015516945A (ja
Filing date
Publication date
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Priority claimed from PCT/US2013/030688 external-priority patent/WO2013138413A1/en
Publication of JP2015516945A publication Critical patent/JP2015516945A/ja
Publication of JP2015516945A5 publication Critical patent/JP2015516945A5/ja
Application granted granted Critical
Publication of JP6140266B2 publication Critical patent/JP6140266B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2015500539A 2012-03-14 2013-03-13 不斉相間移動触媒としてのビス四級シンコナアルカロイド塩 Active JP6140266B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261610746P 2012-03-14 2012-03-14
US61/610,746 2012-03-14
PCT/US2013/030688 WO2013138413A1 (en) 2012-03-14 2013-03-13 Bis-quarternary cinchona alkaloid salts as asymmetric phase transfer catalysts

Publications (3)

Publication Number Publication Date
JP2015516945A JP2015516945A (ja) 2015-06-18
JP2015516945A5 true JP2015516945A5 (enExample) 2016-05-12
JP6140266B2 JP6140266B2 (ja) 2017-05-31

Family

ID=49161748

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015500539A Active JP6140266B2 (ja) 2012-03-14 2013-03-13 不斉相間移動触媒としてのビス四級シンコナアルカロイド塩

Country Status (12)

Country Link
US (1) US9376431B2 (enExample)
EP (4) EP3680240A1 (enExample)
JP (1) JP6140266B2 (enExample)
KR (2) KR102061180B1 (enExample)
CN (1) CN104144929B (enExample)
AU (6) AU2013232191B2 (enExample)
BR (1) BR112014021828B8 (enExample)
CA (1) CA2865941A1 (enExample)
ES (1) ES2806150T3 (enExample)
MX (1) MX351657B (enExample)
RU (1) RU2667909C2 (enExample)
WO (1) WO2013138413A1 (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI487706B (zh) * 2010-11-12 2015-06-11 Merck Sharp & Dohme 六氫吡啶酮甲醯胺氮雜茚滿cgrp受體拮抗劑
US9487523B2 (en) 2012-03-14 2016-11-08 Merck Sharp & Dohme Corp. Process for making CGRP receptor antagonists
US9174989B2 (en) 2012-05-09 2015-11-03 Merck Sharp & Dohme Corp. Process for making CGRP receptor antagonists
CA2937315A1 (en) 2014-02-05 2015-08-13 Merck Sharp & Dohme Corp. Tablet formulation for cgrp-active compounds
US12168004B2 (en) 2014-02-05 2024-12-17 Merck Sharp & Dohme Llc Treatment of migraine
MX384019B (es) * 2016-06-07 2025-03-14 Pirelli Neumatico para ruedas de vehiculos.
CA3065683A1 (en) 2017-05-30 2018-12-06 Millennium Pharmaceuticals, Inc. Method for producing optically active compound
US12383545B1 (en) 2018-06-08 2025-08-12 Allergan Pharmaceuticals International Limited Treatment of migraine
CN109180606B (zh) * 2018-09-30 2021-04-06 浙江工业大学 一类具有光学活性的β-氨基酮的合成方法
CA3181189A1 (en) * 2020-05-06 2021-11-11 Amgen Inc. Synthesis of vinylic alcohol intermediates
AU2021319090A1 (en) 2020-07-29 2023-03-02 Allergan Pharmaceuticals International Limited Treatment of migraine
AU2021409718A1 (en) 2020-12-22 2023-07-13 Allergan Pharmaceuticals International Limited Treatment of migraine
JP2024533756A (ja) 2021-09-27 2024-09-12 アラガン ファーマスーティカルズ インターナショナル リミテッド アトゲパントを含む片頭痛の併用療法
CN115974867B (zh) * 2023-01-31 2025-11-28 成都大学 一种手性相转移催化剂及其制备方法和应用

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE170173T1 (de) * 1990-01-22 1998-09-15 Hoechst Marion Roussel Inc Verfahren zur enantioselektiven synthese alkylierter oxindole zur verwendung als zwischenprodukte bei der herstellung von physostigminen
US6313247B1 (en) * 1996-06-05 2001-11-06 Wolfgang Lindner Cinchonan based chiral selectors for separation of stereoisomers
US6596870B2 (en) * 2000-07-13 2003-07-22 Brandeis University Asymmetric synthetic methods based on phase transfer catalysis
WO2005000109A2 (en) * 2003-06-27 2005-01-06 University Of Maryland Biotechnology Institute Quaternary nitrogen heterocyclic compounds for detecting aqueous monosaccharides in physiological fluids
GB0601286D0 (en) * 2006-01-23 2006-03-01 Sandoz Ag Asymmetric synthesis
PL213306B1 (pl) * 2008-02-04 2013-02-28 Politechnika Lodzka Sposób otrzymywania wzbogaconych enancjomerycznie produktów kondensacji z kwasów racemicznych lub kwasów o niskiej czystosci enancjomerycznej
WO2011005731A2 (en) * 2009-07-08 2011-01-13 Merck Sharp & Dohme Corp. Process for making cgrp receptor antagonist
US9487523B2 (en) 2012-03-14 2016-11-08 Merck Sharp & Dohme Corp. Process for making CGRP receptor antagonists
US9174989B2 (en) 2012-05-09 2015-11-03 Merck Sharp & Dohme Corp. Process for making CGRP receptor antagonists

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