SI2522663T1 - Vmesne spojine za pripravo halihondrina B - Google Patents
Vmesne spojine za pripravo halihondrina BInfo
- Publication number
- SI2522663T1 SI2522663T1 SI200531971T SI200531971T SI2522663T1 SI 2522663 T1 SI2522663 T1 SI 2522663T1 SI 200531971 T SI200531971 T SI 200531971T SI 200531971 T SI200531971 T SI 200531971T SI 2522663 T1 SI2522663 T1 SI 2522663T1
- Authority
- SI
- Slovenia
- Prior art keywords
- halichondrin
- intermediates
- preparation
- Prior art date
Links
- ZBLLGPUWGCOJNG-UHFFFAOYSA-N Halichondrin B Natural products CC1CC2(CC(C)C3OC4(CC5OC6C(CC5O4)OC7CC8OC9CCC%10OC(CC(C(C9)C8=C)C%11%12CC%13OC%14C(OC%15CCC(CC(=O)OC7C6C)OC%15C%14O%11)C%13O%12)CC%10=C)CC3O2)OC%16OC(CC1%16)C(O)CC(O)CO ZBLLGPUWGCOJNG-UHFFFAOYSA-N 0.000 title 1
- FXNFULJVOQMBCW-VZBLNRDYSA-N halichondrin b Chemical compound O([C@@H]1[C@@H](C)[C@@H]2O[C@@H]3C[C@@]4(O[C@H]5[C@@H](C)C[C@@]6(C[C@@H]([C@@H]7O[C@@H](C[C@@H]7O6)[C@@H](O)C[C@@H](O)CO)C)O[C@H]5C4)O[C@@H]3C[C@@H]2O[C@H]1C[C@@H]1C(=C)[C@H](C)C[C@@H](O1)CC[C@H]1C(=C)C[C@@H](O1)CC1)C(=O)C[C@H](O2)CC[C@H]3[C@H]2[C@H](O2)[C@@H]4O[C@@H]5C[C@@]21O[C@@H]5[C@@H]4O3 FXNFULJVOQMBCW-VZBLNRDYSA-N 0.000 title 1
- 239000000543 intermediate Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/40—Halogenated unsaturated alcohols
- C07C33/42—Halogenated unsaturated alcohols acyclic
- C07C33/423—Halogenated unsaturated alcohols acyclic containing only double bonds as unsaturation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/28—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/72—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 spiro-condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/12—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
- C07D493/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/12—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
- C07D493/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/22—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C07F7/1872—Preparation; Treatments not provided for in C07F7/20
- C07F7/188—Preparation; Treatments not provided for in C07F7/20 by reactions involving the formation of Si-O linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/26—Acyclic or carbocyclic radicals, substituted by hetero rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Compounds Of Unknown Constitution (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57664204P | 2004-06-03 | 2004-06-03 | |
US62676904P | 2004-11-10 | 2004-11-10 | |
US66330005P | 2005-03-18 | 2005-03-18 | |
EP12178696.6A EP2522663B1 (en) | 2004-06-03 | 2005-06-03 | Intermediates for the preparation of halichondrin B |
Publications (1)
Publication Number | Publication Date |
---|---|
SI2522663T1 true SI2522663T1 (sl) | 2015-08-31 |
Family
ID=34972515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200531971T SI2522663T1 (sl) | 2004-06-03 | 2005-06-03 | Vmesne spojine za pripravo halihondrina B |
Country Status (15)
Country | Link |
---|---|
US (10) | USRE46965E1 (sl) |
EP (4) | EP3587408A1 (sl) |
JP (5) | JP5226304B2 (sl) |
KR (1) | KR101434673B1 (sl) |
CN (2) | CN104876896A (sl) |
AU (1) | AU2005250487B2 (sl) |
CA (3) | CA2935786C (sl) |
ES (1) | ES2748200T3 (sl) |
HR (1) | HRP20150543T1 (sl) |
HU (1) | HUE046436T2 (sl) |
IL (5) | IL180252A (sl) |
PL (1) | PL2522663T3 (sl) |
RS (1) | RS54054B1 (sl) |
SI (1) | SI2522663T1 (sl) |
WO (1) | WO2005118565A1 (sl) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2272839B1 (en) * | 1998-06-17 | 2012-08-22 | Eisai R&D Management Co., Ltd. | Intermediate compounds for the preparation of halichondrin analogs |
EP3587408A1 (en) | 2004-06-03 | 2020-01-01 | Eisai R&D Management Co., Ltd. | Intermediates for the preparation of halichondrin b |
US8093410B2 (en) * | 2007-10-03 | 2012-01-10 | Eisai R&D Management Co., Ltd. | Intermediates and methods for the synthesis of halichondrin B analogs |
RU2010118063A (ru) * | 2007-11-16 | 2011-12-27 | ЭЙСАЙ Ар энд Ди МЕНЕДЖМЕНТ КО., ЛТД. (JP) | Новое промежуточное соединение для синтеза аналога галихондрина в и новая реакция десульфонилирования, применяемая для получения промежуточного соединения |
RU2517167C2 (ru) | 2008-04-04 | 2014-05-27 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Аналоги галихондрина в |
ME02518B (me) | 2009-03-30 | 2017-02-20 | Eisai R&D Man Co Ltd | Smeša lipozoma |
US8765974B2 (en) | 2009-04-14 | 2014-07-01 | Nissan Chemical Industries, Ltd. | Method for producing tetrahydropyran compound and intermediate thereof |
EP2528914B1 (en) | 2010-01-26 | 2014-06-11 | Eisai R&D Management Co., Ltd. | Furo[3,2-b]pyrane derivatives useful in the synthesis of halichondrin b analogs |
WO2012147900A1 (en) | 2011-04-28 | 2012-11-01 | Eisai R&D Management Co., Ltd. | Microreactor process for halichondrin b analog synthesis |
WO2013053102A1 (en) | 2011-10-11 | 2013-04-18 | Givaudan Sa | Improvements in or relating to organic compounds |
EP2785687B1 (en) | 2011-11-30 | 2019-02-20 | Sandoz AG | Process for preparation of (3r)-2,4-di-leaving group-3-methylbut-1-ene |
WO2013086634A1 (en) | 2011-12-16 | 2013-06-20 | Alphora Research Inc. | Process for preparation of 3-((2s,5s)-4-methylene-5-(3-oxopropyl)tetrahydrofuran-2-yl) propanol derivatives and intermediates useful thereof |
CA2860446C (en) * | 2011-12-29 | 2017-01-10 | Alphora Research Inc. | 2-((2s,3s,4r,5r)-5-((s)-3-amino-2-hydroxyprop-1-yl)-4-methoxy-3-(phenylsulfonylmethyl)tetrahydrofuran-2-yl)acetaldehyde derivatives and process for their preparation |
AU2013239290B2 (en) | 2012-03-30 | 2017-08-03 | Sandoz Ag | Synthetic process for preparation of macrocyclic C1-keto analogs of Halichondrin B and intermediates useful therein |
EP2928464A1 (en) | 2012-12-04 | 2015-10-14 | Eisai R&D Management Co., Ltd. | Use of eribulin in the treatment of breast cancer |
KR102265952B1 (ko) * | 2013-06-26 | 2021-06-16 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 암 치료 병용요법으로서 에리불린 및 렌바티닙의 용도 |
JP6511613B2 (ja) | 2013-07-03 | 2019-05-15 | サンド・アクチエンゲゼルシヤフト | ハリコンドリンBの大環状C1−ケト類似体の製造のための合成方法及び該方法に有用な中間体、例えば−SO2−(p−トリル)基を含有する中間体 |
BR112016009452B1 (pt) | 2013-11-04 | 2022-06-07 | Eisai R&D Management Co., Ltd | Métodos de preparar intermediários na síntese de eribulina, métodos de preparar eribulina e mesilato de eribulina, e compostos intermediários |
CN105916861B (zh) | 2013-12-06 | 2018-12-14 | 卫材R&D管理有限公司 | 可用于合成软海绵素b类似物的方法 |
TW201617326A (zh) | 2014-03-06 | 2016-05-16 | Alphora研發股份有限公司 | (s)-1-((2r,3r,4s,5s)-5-烯丙-3-甲氧-4-(對甲苯磺醯甲基)四氫呋喃-2-基)-3-氨基丙-2-醇之結晶衍生物 |
AU2015267099B2 (en) | 2014-05-28 | 2020-08-27 | Eisai R&D Management Co., Ltd | Use of eribulin in the treatment of cancer |
EP3160970A4 (en) | 2014-06-30 | 2017-12-27 | President and Fellows of Harvard College | Synthesis of halichondrin analogs and uses thereof |
WO2016038624A1 (en) * | 2014-09-09 | 2016-03-17 | Cipla Limited | "process for the preparation of macrocyclic ketone analogs of halichondrin b or pharmaceutically acceptable salts and intermediates thereof" |
WO2016141209A1 (en) | 2015-03-04 | 2016-09-09 | Merck Sharp & Dohme Corp. | Combination of a pd-1 antagonist and eribulin for treating cancer |
US10344038B2 (en) | 2015-04-30 | 2019-07-09 | President And Fellows Of Harvard College | Chromium-mediated coupling and application to the synthesis of halichondrins |
CN107849057B (zh) | 2015-05-07 | 2020-11-10 | 卫材R&D管理有限公司 | 用于合成软海绵素大环内酯的大环化反应及中间体和其他片段 |
KR101777634B1 (ko) * | 2016-01-18 | 2017-09-12 | 연성정밀화학(주) | 3-((2s,5s)-4-메틸렌-5-(3-옥소프로필)테트라히드로퓨란-2-일)프로판올 유도체의 제조방법 및 이를 위한 중간체 |
JP6786610B2 (ja) | 2016-02-12 | 2020-11-18 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | エリブリンの合成における中間体および関連する合成方法 |
KR20220101204A (ko) | 2016-03-02 | 2022-07-19 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 에리불린-기반 항체-약물 콘주게이트 및 사용 방법 |
JP7015237B2 (ja) | 2016-04-28 | 2022-02-02 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 腫瘍の成長を抑制する方法 |
KR20190009326A (ko) * | 2016-05-26 | 2019-01-28 | 닥터 레디스 레보러터리즈 리미티드 | 에리불린 및 그의 중간체의 제조방법 |
MX2018016329A (es) | 2016-06-30 | 2019-09-18 | Eisai R&D Man Co Ltd | Reaccion de prins e intermediarios utiles en la sintesis de macrolidos de halicondrina y analogos de los mismos. |
MX2019003994A (es) | 2016-10-14 | 2019-09-19 | Merck Sharp & Dohme | Combinacion de un antagonista de proteina de muerte programada-1 (pd-1) y eribulina para el tratamiento de cancer urotelial. |
JP6978758B2 (ja) | 2016-11-11 | 2021-12-08 | プレジデント アンド フェローズ オブ ハーバード カレッジ | パラジウム媒介ケトール化 |
CN110167536A (zh) * | 2016-11-23 | 2019-08-23 | 雷迪博士实验室有限公司 | 艾日布林及其中间体的制备方法 |
JP6920699B2 (ja) * | 2017-01-02 | 2021-08-18 | ヨンスン ファイン ケミカル カンパニー,リミテッド | エリブリンメシル酸塩の製造中間体及びその製造方法 |
KR101880939B1 (ko) * | 2017-01-02 | 2018-08-17 | 연성정밀화학(주) | 에리불린 메실산염의 제조 중간체 및 그의 제조방법 |
US9938288B1 (en) | 2017-04-05 | 2018-04-10 | President And Fellows Of Harvard College | Macrocyclic compound and uses thereof |
PE20200602A1 (es) | 2017-04-05 | 2020-03-10 | Harvard College | Compuesto macrociclico y sus usos |
CN108948064B (zh) | 2017-05-17 | 2021-02-02 | 上海时莱生物技术有限公司 | 一种艾日布林中间体及其制备方法 |
EP4169924A3 (en) | 2017-07-06 | 2023-07-05 | President And Fellows Of Harvard College | Synthesis of halichondrins |
US11498892B2 (en) | 2017-07-06 | 2022-11-15 | President And Fellows Of Harvard College | Fe/Cu-mediated ketone synthesis |
US20190046513A1 (en) | 2017-08-10 | 2019-02-14 | Huya Bioscience International, Llc | Combination therapies of hdac inhibitors and tubulin inhibitors |
WO2019093776A1 (ko) | 2017-11-09 | 2019-05-16 | 연성정밀화학(주) | 에리불린 메실산염의 제조 중간체 및 그의 제조방법 |
EP3710454B1 (en) | 2017-11-15 | 2024-01-03 | President And Fellows Of Harvard College | Macrocyclic compounds and uses thereof |
US11419856B2 (en) | 2017-11-20 | 2022-08-23 | Basilea Pharmaceutica International AG | Pharmaceutical combinations for use in the treatment of neoplastic diseases |
US11008296B2 (en) | 2017-11-21 | 2021-05-18 | Natco Pharma Limited | Intermediates for the preparation of eribulin thereof |
CN107973804B (zh) * | 2017-11-29 | 2020-07-03 | 戊言医药科技(上海)有限公司 | 艾瑞布林中间体的合成方法 |
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 |
CN110218213B (zh) * | 2018-03-02 | 2020-09-04 | 北京天一绿甫医药科技有限公司 | 吡喃稠环类化合物、其制备方法和用途 |
WO2019211877A1 (en) | 2018-05-03 | 2019-11-07 | Cipla Limited | Process for the preparation of macrocyclic ketone analogs of halichondrin b |
WO2020008382A1 (en) * | 2018-07-04 | 2020-01-09 | Dr. Reddy’S Laboratories Limited | Process for preparation of eribulin and intermediates thereof |
CN111285894B (zh) * | 2018-12-10 | 2021-03-05 | 北京天一绿甫医药科技有限公司 | 用于制备软海绵素类化合物的中间体及其制备方法 |
CN111454277A (zh) * | 2019-01-21 | 2020-07-28 | 上海茂晟康慧科技有限公司 | 一种艾日布林中间体er806047的合成方法 |
CN111689982B (zh) * | 2019-03-15 | 2023-04-07 | 博瑞生物医药(苏州)股份有限公司 | 艾日布林中间体及其制备方法 |
US11447499B2 (en) | 2019-06-14 | 2022-09-20 | Rk Pharma Inc. | Process for the preparation of eribulin mesylate intermediate |
JP2022537785A (ja) | 2019-06-21 | 2022-08-29 | カウンスィル オブ サイエンティフィック アンド インダストリアル リサーチ | ホモプロパルギルアルコールを調製するための化学酵素的プロセス |
US11083705B2 (en) | 2019-07-26 | 2021-08-10 | Eisai R&D Management Co., Ltd. | Pharmaceutical composition for treating tumor |
CN112409302A (zh) * | 2019-08-22 | 2021-02-26 | 上海茂晟康慧科技有限公司 | 一种艾日布林中间体er806060的合成方法 |
CN113024576B (zh) * | 2019-12-09 | 2024-03-29 | 南通诺泰生物医药技术有限公司 | 艾日布林及其中间体的制备方法 |
CN113024589A (zh) * | 2019-12-09 | 2021-06-25 | 南通诺泰生物医药技术有限公司 | 艾日布林及其中间体的制备方法 |
CN113121555B (zh) * | 2020-01-16 | 2024-03-08 | 南通诺泰生物医药技术有限公司 | 通过微通道反应器制备艾日布林中间体的方法 |
CN113135876B (zh) * | 2020-01-16 | 2024-05-17 | 南通诺泰生物医药技术有限公司 | 艾日布林及其中间体的制备方法 |
CN113549101A (zh) * | 2020-04-26 | 2021-10-26 | 博瑞生物医药(苏州)股份有限公司 | 艾日布林及其中间体的制备方法 |
CA3098164A1 (en) * | 2020-11-05 | 2022-05-05 | Eurofins Cdmo Alphora Inc. | Process for preparation of advanced intermediate for eribulin synthesys |
IL279168B (en) * | 2020-12-02 | 2022-04-01 | Finetech Pharmaceutical Ltd | A process for the preparation of eribulin |
CN114213449A (zh) * | 2021-12-28 | 2022-03-22 | 南京格亚医药科技有限公司 | 一种甲磺酸艾日布林关键中间体异构体的制备方法 |
CN114409617A (zh) * | 2021-12-28 | 2022-04-29 | 南京格亚医药科技有限公司 | 一种甲磺酸艾日布林关键中间体异构体的制备方法 |
WO2023157015A1 (en) * | 2022-02-17 | 2023-08-24 | Natco Pharma Limited | An improved process for the preparation of eribulin intermediates |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436238A (en) | 1992-03-12 | 1995-07-25 | President And Fellows Of Harvard College | Halichondrins and related compounds |
US5338865A (en) * | 1992-03-12 | 1994-08-16 | President And Fellows Of Harvard College | Synthesis of halichondrin B and norhalichondrin B |
GB9206244D0 (en) | 1992-03-23 | 1992-05-06 | Pharma Mar Sa | Cytotoxic compound from a marine sponge |
TW255880B (sl) | 1992-09-09 | 1995-09-01 | Hoechst Ag | |
JP2001500498A (ja) | 1996-09-06 | 2001-01-16 | イーライ・リリー・アンド・カンパニー | 触媒選択的スルホニル化法 |
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 |
US8097648B2 (en) | 1998-06-17 | 2012-01-17 | Eisai R&D Management Co., Ltd. | Methods and compositions for use in treating cancer |
US6653341B1 (en) | 1998-06-17 | 2003-11-25 | Eisai Co., Ltd. | Methods and compositions for use in treating cancer |
EP2272839B1 (en) | 1998-06-17 | 2012-08-22 | Eisai R&D Management Co., Ltd. | Intermediate compounds for the preparation of halichondrin analogs |
DE10106647A1 (de) * | 2001-02-12 | 2002-08-22 | Univ Hannover | Ratjadon-Derivate zum Hemmen des Zellwachstums |
EP3587408A1 (en) | 2004-06-03 | 2020-01-01 | Eisai R&D Management Co., Ltd. | Intermediates for the preparation of halichondrin b |
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 |
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 |
US8093410B2 (en) | 2007-10-03 | 2012-01-10 | Eisai R&D Management Co., Ltd. | Intermediates and methods for the synthesis of halichondrin B analogs |
RU2010118063A (ru) | 2007-11-16 | 2011-12-27 | ЭЙСАЙ Ар энд Ди МЕНЕДЖМЕНТ КО., ЛТД. (JP) | Новое промежуточное соединение для синтеза аналога галихондрина в и новая реакция десульфонилирования, применяемая для получения промежуточного соединения |
RU2517167C2 (ru) | 2008-04-04 | 2014-05-27 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Аналоги галихондрина в |
EP2528914B1 (en) | 2010-01-26 | 2014-06-11 | Eisai R&D Management Co., Ltd. | Furo[3,2-b]pyrane derivatives useful in the synthesis of halichondrin b analogs |
WO2012147900A1 (en) | 2011-04-28 | 2012-11-01 | Eisai R&D Management Co., Ltd. | Microreactor process for halichondrin b analog synthesis |
EP2785687B1 (en) | 2011-11-30 | 2019-02-20 | Sandoz AG | Process for preparation of (3r)-2,4-di-leaving group-3-methylbut-1-ene |
AU2013239290B2 (en) | 2012-03-30 | 2017-08-03 | Sandoz Ag | Synthetic process for preparation of macrocyclic C1-keto analogs of Halichondrin B and intermediates useful therein |
EP2928464A1 (en) | 2012-12-04 | 2015-10-14 | Eisai R&D Management Co., Ltd. | Use of eribulin in the treatment of breast cancer |
JP6511613B2 (ja) | 2013-07-03 | 2019-05-15 | サンド・アクチエンゲゼルシヤフト | ハリコンドリンBの大環状C1−ケト類似体の製造のための合成方法及び該方法に有用な中間体、例えば−SO2−(p−トリル)基を含有する中間体 |
BR112016009452B1 (pt) | 2013-11-04 | 2022-06-07 | Eisai R&D Management Co., Ltd | Métodos de preparar intermediários na síntese de eribulina, métodos de preparar eribulina e mesilato de eribulina, e compostos intermediários |
CN105916861B (zh) | 2013-12-06 | 2018-12-14 | 卫材R&D管理有限公司 | 可用于合成软海绵素b类似物的方法 |
EP3113775A4 (en) | 2014-03-03 | 2017-08-23 | Eisai R&D Management Co., Ltd. | Use of eribulin and mtor inhibitors as combination therapy for the treatment of cancer |
JP6648040B2 (ja) | 2014-05-28 | 2020-02-14 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | がん治療のための併用療法としてのエリブリン及びポリ(adpリボース)ポリメラーゼ(parp)阻害剤の使用 |
AU2015267099B2 (en) | 2014-05-28 | 2020-08-27 | Eisai R&D Management Co., Ltd | Use of eribulin in the treatment of cancer |
WO2016141209A1 (en) | 2015-03-04 | 2016-09-09 | Merck Sharp & Dohme Corp. | Combination of a pd-1 antagonist and eribulin for treating cancer |
CN107849057B (zh) | 2015-05-07 | 2020-11-10 | 卫材R&D管理有限公司 | 用于合成软海绵素大环内酯的大环化反应及中间体和其他片段 |
JP6786610B2 (ja) | 2016-02-12 | 2020-11-18 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | エリブリンの合成における中間体および関連する合成方法 |
MX2018016329A (es) | 2016-06-30 | 2019-09-18 | Eisai R&D Man Co Ltd | Reaccion de prins e intermediarios utiles en la sintesis de macrolidos de halicondrina y analogos de los mismos. |
-
2005
- 2005-06-03 EP EP19172746.0A patent/EP3587408A1/en not_active Withdrawn
- 2005-06-03 CA CA2935786A patent/CA2935786C/en active Active
- 2005-06-03 JP JP2007515643A patent/JP5226304B2/ja active Active
- 2005-06-03 WO PCT/US2005/019669 patent/WO2005118565A1/en active Application Filing
- 2005-06-03 EP EP12178696.6A patent/EP2522663B1/en active Active
- 2005-06-03 EP EP05760356A patent/EP1771431A1/en not_active Ceased
- 2005-06-03 US US13/924,892 patent/USRE46965E1/en active Active
- 2005-06-03 CN CN201410850876.5A patent/CN104876896A/zh active Pending
- 2005-06-03 PL PL12178696T patent/PL2522663T3/pl unknown
- 2005-06-03 CA CA2567984A patent/CA2567984C/en active Active
- 2005-06-03 ES ES15159875T patent/ES2748200T3/es active Active
- 2005-06-03 US US13/495,909 patent/USRE45324E1/en active Active
- 2005-06-03 CA CA3028453A patent/CA3028453C/en active Active
- 2005-06-03 US US11/628,396 patent/US7982060B2/en not_active Ceased
- 2005-06-03 HU HUE15159875A patent/HUE046436T2/hu unknown
- 2005-06-03 CN CN201010236637.2A patent/CN101899026B/zh active Active
- 2005-06-03 RS RS20150371A patent/RS54054B1/en unknown
- 2005-06-03 EP EP15159875.2A patent/EP2949652B1/en active Active
- 2005-06-03 KR KR1020077000085A patent/KR101434673B1/ko active IP Right Review Request
- 2005-06-03 SI SI200531971T patent/SI2522663T1/sl unknown
- 2005-06-03 AU AU2005250487A patent/AU2005250487B2/en active Active
-
2006
- 2006-12-21 IL IL180252A patent/IL180252A/en active IP Right Grant
-
2011
- 2011-06-29 US US13/171,971 patent/US20120029213A1/en not_active Abandoned
-
2012
- 2012-05-21 US US13/476,276 patent/US8445701B2/en active Active
- 2012-11-21 JP JP2012255149A patent/JP5705814B2/ja active Active
-
2013
- 2013-04-23 US US13/868,641 patent/US8618313B2/en active Active
- 2013-07-09 IL IL227402A patent/IL227402A/en active IP Right Grant
- 2013-07-14 IL IL227474A patent/IL227474A/en active IP Right Grant
- 2013-12-04 US US14/096,549 patent/US8884031B2/en active Active
-
2014
- 2014-04-10 US US14/250,086 patent/US8975422B2/en active Active
- 2014-11-04 JP JP2014224099A patent/JP5964926B2/ja active Active
-
2015
- 2015-02-17 US US14/624,171 patent/US9303050B2/en not_active Ceased
- 2015-05-20 HR HRP20150543TT patent/HRP20150543T1/hr unknown
-
2016
- 2016-05-09 JP JP2016093633A patent/JP6138316B2/ja active Active
- 2016-09-04 IL IL247620A patent/IL247620B/en not_active IP Right Cessation
-
2017
- 2017-03-07 JP JP2017042492A patent/JP6306235B2/ja active Active
-
2018
- 2018-04-03 US US15/944,480 patent/USRE47797E1/en active Active
-
2019
- 2019-06-24 IL IL267606A patent/IL267606B/en active IP Right Grant
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL180252A0 (en) | Intermediates for the preparation of halichondrin b | |
PT1802579E (pt) | Derivados da 3-arilaminopiridina | |
IL188330A0 (en) | Processes for the preparation of | |
IL204791A0 (en) | Intermediates and methods for the synthesis of halichondrin b analogs | |
HUE061093T2 (hu) | Eljárás katalitikus anyagok elõállítására | |
IL183176A0 (en) | Methods for the preparation of sevoflurane | |
HK1163672A1 (en) | Processes for the preparation of compounds | |
IL211796A (en) | Intermediates for the preparation of oxidized phospholipids | |
EP1893625A4 (en) | PROCESS FOR THE PREPARATION OF 9-DEAZAPURINE DERIVATIVES | |
IL185029A0 (en) | Preparation of tadalafil intermediates | |
HUP0500537A3 (en) | Process for the preparation of rosuvastatin via new intermediates | |
IL181185A0 (en) | Novel polymorphs of azabicyclohexane | |
IL184715A0 (en) | Process for the preparation of intermediates | |
EP1853559A4 (en) | IMPROVED PROCESS FOR THE PREPARATION OF ATORVASTATIN AND INTERMEDIATES THEREOF | |
EP1932527A4 (en) | USE OF PHTHALIDE DERIVATIVES | |
IL187832A0 (en) | Methods and intermediates for the preparation of optionally radio- labeled imatinib | |
HU0401379D0 (en) | Process for the preparation of risperidon | |
ITMI20041086A1 (it) | Procedimento per la preparazione di idrocarbilalogenuri | |
PL1591434T3 (pl) | Nowe 1-metoksy-2-fenylo-etyleny przydatne do otrzymywania 5-karboksyaldehydu-2-3-dihydrobenzoksepin | |
GB2414238B (en) | Method for the preparation of trilostane | |
HK1071368A1 (en) | Method for the preparation of citalopram | |
AU2004901802A0 (en) | Process for the preparation of intermediates | |
SI1732916T1 (sl) | Postopek za pripravo alkoksikarbonilmetoksi-ciklopentanov | |
AU2006332419A1 (en) | The use of phthalide derivatives | |
TWM291594U (en) | Improved structure of transformer |