JP2019524674A5 - - Google Patents

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JP2019524674A5
JP2019524674A5 JP2018568296A JP2018568296A JP2019524674A5 JP 2019524674 A5 JP2019524674 A5 JP 2019524674A5 JP 2018568296 A JP2018568296 A JP 2018568296A JP 2018568296 A JP2018568296 A JP 2018568296A JP 2019524674 A5 JP2019524674 A5 JP 2019524674A5
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JP7068204B2 (ja
JP2019524674A (ja
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Priority claimed from PCT/US2017/040401 external-priority patent/WO2018006031A1/en
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Priority to JP2022073976A priority Critical patent/JP7440563B2/ja
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Priority to JP2024020885A priority patent/JP2024056892A/ja
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JP2018568296A 2016-06-30 2017-06-30 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体 Active JP7068204B2 (ja)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2022073976A JP7440563B2 (ja) 2016-06-30 2022-04-28 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体
JP2024020885A JP2024056892A (ja) 2016-06-30 2024-02-15 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662357031P 2016-06-30 2016-06-30
US62/357,031 2016-06-30
PCT/US2017/040401 WO2018006031A1 (en) 2016-06-30 2017-06-30 Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof

Related Child Applications (1)

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JP2022073976A Division JP7440563B2 (ja) 2016-06-30 2022-04-28 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体

Publications (3)

Publication Number Publication Date
JP2019524674A JP2019524674A (ja) 2019-09-05
JP2019524674A5 true JP2019524674A5 (OSRAM) 2020-08-06
JP7068204B2 JP7068204B2 (ja) 2022-05-16

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JP2018568296A Active JP7068204B2 (ja) 2016-06-30 2017-06-30 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体
JP2022073976A Active JP7440563B2 (ja) 2016-06-30 2022-04-28 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体
JP2024020885A Pending JP2024056892A (ja) 2016-06-30 2024-02-15 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体

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JP2022073976A Active JP7440563B2 (ja) 2016-06-30 2022-04-28 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体
JP2024020885A Pending JP2024056892A (ja) 2016-06-30 2024-02-15 ハリコンドリンマクロライドおよびその類縁体の合成に有用なプリンス反応および中間体

Country Status (9)

Country Link
US (1) US11136335B2 (OSRAM)
EP (1) EP3478691A4 (OSRAM)
JP (3) JP7068204B2 (OSRAM)
KR (1) KR102404629B1 (OSRAM)
CN (2) CN114805322B (OSRAM)
IL (2) IL263845B (OSRAM)
MX (1) MX390072B (OSRAM)
SG (1) SG11201811671XA (OSRAM)
WO (1) WO2018006031A1 (OSRAM)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE046436T2 (hu) 2004-06-03 2020-02-28 Eisai R&D Man Co Ltd Köztitermékek halikondrin B elõállításához
US8093410B2 (en) 2007-10-03 2012-01-10 Eisai R&D Management Co., Ltd. Intermediates and methods for the synthesis of halichondrin B analogs
RU2579511C2 (ru) 2010-01-26 2016-04-10 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Производные фуро[3,2-в]пирана, применимые в синтезе аналогов
EP3689881B1 (en) 2013-11-04 2022-01-12 Eisai R&D Management Co., Ltd. Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin b
SG10201805024YA (en) 2013-12-06 2018-07-30 Eisai R&D Man Co Ltd Methods useful in the synthesis of halichondrin b analogs
RU2020141025A (ru) 2015-05-07 2020-12-28 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Реакции макроциклизации и промежуточные соединения и другие фрагменты, полезные в синтезе макролидов галихондринов
US10676481B2 (en) 2016-02-12 2020-06-09 Eisai R&D Management Co., Ltd. Intermediates in the synthesis of eribulin and related methods of synthesis
US11542269B2 (en) 2018-01-03 2023-01-03 Eisai R&D Management Co., Ltd. Prins reaction and compounds useful in the synthesis of halichondrin macrolides and analogs thereof
EP3608323B1 (en) * 2018-03-02 2021-11-03 Beijing Tienyi Lufu Pharmatech Co. Ltd. Pyran fused ring compound, preparation method therefor and use thereof

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU652180A1 (ru) 1975-12-16 1979-03-15 Краснодарский политехнический институт 1(Фурил-2,)-2-(2-,, формилфурил-5,, ) этилен или его метильное производное как промежуточный продукт дл синтеза фуран-2,5-дикарбоновой кислоты и способ его получени
US5338865A (en) 1992-03-12 1994-08-16 President And Fellows Of Harvard College Synthesis of halichondrin B and norhalichondrin B
US5436238A (en) 1992-03-12 1995-07-25 President And Fellows Of Harvard College Halichondrins and related compounds
GB9206244D0 (en) 1992-03-23 1992-05-06 Pharma Mar Sa Cytotoxic compound from a marine sponge
TW255880B (OSRAM) 1992-09-09 1995-09-01 Hoechst Ag
US6194586B1 (en) 1996-09-06 2001-02-27 Eli Lilly And Company Selective sulphonation of the primary alcohol of a diol containing both primary and secondary alcohols
US6870058B2 (en) 1996-12-03 2005-03-22 The Trustees Of The University Of Pennsylvania Compounds which mimic the chemical and biological properties of discodermolide
US6653341B1 (en) 1998-06-17 2003-11-25 Eisai Co., Ltd. Methods and compositions for use in treating cancer
DK1087960T3 (da) 1998-06-17 2011-06-14 Eisai R&D Man Co Ltd Makrocykliske analoger og fremgangsmåder til deres anvendelse og fremstilling
US8097648B2 (en) 1998-06-17 2012-01-17 Eisai R&D Management Co., Ltd. Methods and compositions for use in treating cancer
DE10106647A1 (de) 2001-02-12 2002-08-22 Univ Hannover Ratjadon-Derivate zum Hemmen des Zellwachstums
HUE046436T2 (hu) 2004-06-03 2020-02-28 Eisai R&D Man Co Ltd Köztitermékek halikondrin B elõállításához
US20060045846A1 (en) 2004-08-30 2006-03-02 Horstmann Thomas E Reagents and methods for labeling terminal olefins
JP2008522623A (ja) 2004-12-09 2008-07-03 エーザイ株式会社 ハリコンドリンbアナログを使用した癌治療でのチューブリンアイソタイプのスクリーニング
EP1940758B1 (en) 2005-09-26 2012-11-28 Symrise AG Intramolecular prins reaction
WO2008010776A1 (en) 2006-07-21 2008-01-24 Agency For Science, Technology And Research Aigialomycin d and derivatives thereof and their use in treating cancer or malaria or a microbial infection
WO2009014105A1 (ja) 2007-07-20 2009-01-29 Yamada Apiculture Center, Inc. 新規カルボン酸およびそれを有効成分とする抗うつ用組成物
US8093410B2 (en) 2007-10-03 2012-01-10 Eisai R&D Management Co., Ltd. Intermediates and methods for the synthesis of halichondrin B analogs
WO2009064029A1 (en) 2007-11-16 2009-05-22 Eisai R & D Management Co., Ltd. Novel intermediate for halichondrin b analog synthesis and novel desulfonylation reaction used for the intermediate
CA2720632C (en) 2008-04-04 2016-12-20 Eisai R&D Management Co., Ltd. Halichondrin b analogs
JP5371091B2 (ja) 2009-01-23 2013-12-18 三菱レイヨン株式会社 モノスルホン酸エステルの製造方法
RU2579511C2 (ru) 2010-01-26 2016-04-10 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Производные фуро[3,2-в]пирана, применимые в синтезе аналогов
WO2012147900A1 (en) 2011-04-28 2012-11-01 Eisai R&D Management Co., Ltd. Microreactor process for halichondrin b analog synthesis
AU2012344697A1 (en) 2011-11-30 2014-07-10 Alphora Research Inc. Process for preparation of (3R)-2,4-di-leaving group-3-methylbut-1-ene
US9278979B2 (en) 2012-03-30 2016-03-08 Alphora Research Inc. Synthetic process for preparation of macrocyclic C1-keto analogs of halichondrin B and intermediates useful therein
US9850254B2 (en) 2013-07-03 2017-12-26 Sandoz Ag Synthetic process for preparation of macrocyclic C1-keto analogs of Halichondrin B and intermediates useful therein including intermediates containing-SO2-(p-tolyl) groups
EP3689881B1 (en) 2013-11-04 2022-01-12 Eisai R&D Management Co., Ltd. Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin b
SG10201805024YA (en) 2013-12-06 2018-07-30 Eisai R&D Man Co Ltd Methods useful in the synthesis of halichondrin b analogs
EP3191479B1 (en) 2014-09-09 2020-04-08 Cipla Limited "process for the preparation of macrocyclic ketone analogs of halichondrin b or pharmaceutically acceptable salts and intermediates thereof"
RU2020141025A (ru) * 2015-05-07 2020-12-28 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Реакции макроциклизации и промежуточные соединения и другие фрагменты, полезные в синтезе макролидов галихондринов
US10676481B2 (en) 2016-02-12 2020-06-09 Eisai R&D Management Co., Ltd. Intermediates in the synthesis of eribulin and related methods of synthesis
WO2018217894A1 (en) 2017-05-24 2018-11-29 Eisai R&D Management Co., Ltd. Fluorine-labelled halichondrin derivatives and related methods of synthesis
US11542269B2 (en) 2018-01-03 2023-01-03 Eisai R&D Management Co., Ltd. Prins reaction and compounds useful in the synthesis of halichondrin macrolides and analogs thereof

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