IN2014MN02106A - - Google Patents
Download PDFInfo
- Publication number
- IN2014MN02106A IN2014MN02106A IN2106MUN2014A IN2014MN02106A IN 2014MN02106 A IN2014MN02106 A IN 2014MN02106A IN 2106MUN2014 A IN2106MUN2014 A IN 2106MUN2014A IN 2014MN02106 A IN2014MN02106 A IN 2014MN02106A
- Authority
- IN
- India
- Prior art keywords
- compound
- formula
- disclosed
- preparation
- pharmaceutically acceptable
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229930195695 Halichondrin Natural products 0.000 abstract 1
- UFNVPOGXISZXJD-XJPMSQCNSA-N eribulin Chemical compound C([C@H]1CC[C@@H]2O[C@@H]3[C@H]4O[C@H]5C[C@](O[C@H]4[C@H]2O1)(O[C@@H]53)CC[C@@H]1O[C@H](C(C1)=C)CC1)C(=O)C[C@@H]2[C@@H](OC)[C@@H](C[C@H](O)CN)O[C@H]2C[C@@H]2C(=C)[C@H](C)C[C@H]1O2 UFNVPOGXISZXJD-XJPMSQCNSA-N 0.000 abstract 1
- 229960003649 eribulin Drugs 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
Classifications
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/04—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261618004P | 2012-03-30 | 2012-03-30 | |
US201261647127P | 2012-05-15 | 2012-05-15 | |
PCT/CA2013/050254 WO2013142999A1 (en) | 2012-03-30 | 2013-03-28 | Synthetic process for preparation of macrocyclic c1-keto analogs of halichondrin b and intermediates useful therein |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2014MN02106A true IN2014MN02106A (zh) | 2015-09-11 |
Family
ID=49258019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN2106MUN2014 IN2014MN02106A (zh) | 2012-03-30 | 2013-03-28 |
Country Status (8)
Country | Link |
---|---|
US (2) | US9278979B2 (zh) |
EP (1) | EP2831082B1 (zh) |
JP (1) | JP6531911B2 (zh) |
CN (1) | CN104334562A (zh) |
AU (1) | AU2013239290B2 (zh) |
CA (1) | CA2868627C (zh) |
IN (1) | IN2014MN02106A (zh) |
WO (1) | WO2013142999A1 (zh) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RS54054B1 (en) | 2004-06-03 | 2015-10-30 | Eisai R&D Management Co. Ltd. | INTERMEDIATES FOR THE PREPARATION OF HALIHONDRIN B |
SG10201811715YA (en) | 2007-10-03 | 2019-02-27 | Eisai R&D Man Co Ltd | Intermediates and methods for the synthesis of halichondrin b analogs |
SG10201500552PA (en) | 2010-01-26 | 2015-03-30 | Eisai R&D Man Co Ltd | Furo [3, 2 -b] pyrane derivatives useful in the synthesis of halichondrin b analogs |
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 |
CA2857395A1 (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 |
WO2013097042A1 (en) | 2011-12-29 | 2013-07-04 | 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 |
CA2916537C (en) * | 2013-07-03 | 2021-07-27 | Alphora Research Inc. | Synthetic process for preparation of macrocyclic c1-keto analogs of halichondrin b and intermediates useful therein including intermediates containing -so2-(p-tolyl) groups |
CN103483352A (zh) * | 2013-10-18 | 2014-01-01 | 李友香 | 抗肿瘤的药用原料药 |
SG11201603490TA (en) * | 2013-11-04 | 2016-05-30 | Eisai R&D Man Co Ltd | Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin b |
MX376869B (es) | 2013-12-06 | 2025-03-07 | Eisai R&D Man Co Ltd | Metodos utiles en la sintesis de analogos de halicondrina b. |
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 |
WO2016003975A1 (en) | 2014-06-30 | 2016-01-07 | President And Fellows Of Harvard College | Synthesis of halichondrin analogs and uses thereof |
CN105713031B (zh) * | 2014-12-05 | 2021-05-07 | 正大天晴药业集团股份有限公司 | 一种用于制备艾日布林的中间体及其制备方法 |
US10344038B2 (en) | 2015-04-30 | 2019-07-09 | President And Fellows Of Harvard College | Chromium-mediated coupling and application to the synthesis of halichondrins |
CN112250692B (zh) | 2015-05-07 | 2023-08-29 | 卫材R&D管理有限公司 | 可用于合成软海绵素大环内酯的大环化反应以及中间体和其他片段 |
RU2732575C2 (ru) | 2016-02-12 | 2020-09-21 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Промежуточные продукты в синтезе эрибулина и соответствующие способы синтеза |
CN114191428B (zh) | 2016-03-02 | 2024-09-24 | 卫材研究发展管理有限公司 | 基于艾日布林的抗体-药物偶联物和使用方法 |
BR112018074287A2 (pt) * | 2016-05-26 | 2019-06-18 | Dr Reddys Laboratories Ltd | processo para preparação de eribulina e intermediários da mesma |
SG11201811671XA (en) | 2016-06-30 | 2019-01-30 | Eisai R&D Man Co Ltd | Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof |
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 |
KR20190084065A (ko) | 2016-11-23 | 2019-07-15 | 닥터 레디스 레보러터리즈 리미티드 | 에리불린 및 그 중간체의 제조방법 |
CN108658956B (zh) * | 2017-03-28 | 2021-02-02 | 上海时莱生物技术有限公司 | 艾日布林中间体及其制备方法 |
US9938288B1 (en) | 2017-04-05 | 2018-04-10 | President And Fellows Of Harvard College | Macrocyclic compound and uses thereof |
PL3606928T3 (pl) | 2017-04-05 | 2023-02-06 | President And Fellows Of Harvard College | Związek makrocykliczny i jego zastosowania |
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 |
WO2018217894A1 (en) * | 2017-05-24 | 2018-11-29 | Eisai R&D Management Co., Ltd. | Fluorine-labelled halichondrin derivatives and related methods of synthesis |
MX2020000142A (es) | 2017-07-06 | 2020-07-22 | Harvard College | Sintesis de halicondrinas. |
US11498892B2 (en) | 2017-07-06 | 2022-11-15 | President And Fellows Of Harvard College | Fe/Cu-mediated ketone synthesis |
CN117924310A (zh) | 2017-11-15 | 2024-04-26 | 哈佛大学的校长及成员们 | 大环化合物及其用途 |
IL275729B2 (en) | 2018-01-03 | 2023-09-01 | Eisai R&D Man Co Ltd | Prins reaction and compounds useful in the synthesis of helicondrin macrolides and their analogs |
IL279168B (en) | 2020-12-02 | 2022-04-01 | Finetech Pharmaceutical Ltd | A process for the preparation of eribulin |
CN114213429B (zh) * | 2021-12-22 | 2023-06-20 | 苏州正济药业有限公司 | 一种甲磺酸艾立布林杂质的制备方法 |
WO2024153123A1 (zh) * | 2023-01-17 | 2024-07-25 | 成都百利多特生物药业有限责任公司 | 一种艾日布林类药物的偶联物 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
CN1103755C (zh) | 1993-07-09 | 2003-03-26 | 桑拉米克斯实验公司 | 维生素d的新型结构类似物 |
EP1087960B1 (en) * | 1998-06-17 | 2011-03-23 | Eisai R&D Management Co., Ltd. | Macrocyclic analogs and methods of their use and preparation |
US7001982B2 (en) | 2003-03-31 | 2006-02-21 | Council Of Scientific And Industrial Research | Non-natural C-linked carbo-β-peptides with robust secondary structures |
RS54054B1 (en) | 2004-06-03 | 2015-10-30 | Eisai R&D Management Co. Ltd. | INTERMEDIATES FOR THE PREPARATION OF HALIHONDRIN B |
US20060045846A1 (en) * | 2004-08-30 | 2006-03-02 | Horstmann Thomas E | Reagents and methods for labeling terminal olefins |
BRPI0911269A2 (pt) * | 2008-04-04 | 2015-09-29 | Eisai R&D Man Co Ltd | análogos de halicondrina b |
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 |
CA2857395A1 (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 |
WO2013097042A1 (en) * | 2011-12-29 | 2013-07-04 | 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 |
TW201514159A (zh) | 2013-05-15 | 2015-04-16 | Alphora Res Inc | 3-((2s,5s)-4-亞甲基-5-(3-氧代丙基)四氫呋喃-2-基)丙醇衍生物、其製備及對其有用的中間體 |
-
2013
- 2013-03-28 CA CA2868627A patent/CA2868627C/en active Active
- 2013-03-28 EP EP13769493.1A patent/EP2831082B1/en not_active Not-in-force
- 2013-03-28 US US14/389,439 patent/US9278979B2/en not_active Expired - Fee Related
- 2013-03-28 AU AU2013239290A patent/AU2013239290B2/en not_active Ceased
- 2013-03-28 CN CN201380028907.2A patent/CN104334562A/zh active Pending
- 2013-03-28 JP JP2015502027A patent/JP6531911B2/ja not_active Expired - Fee Related
- 2013-03-28 WO PCT/CA2013/050254 patent/WO2013142999A1/en active Application Filing
- 2013-03-28 IN IN2106MUN2014 patent/IN2014MN02106A/en unknown
-
2016
- 2016-02-04 US US15/015,161 patent/US9695187B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
EP2831082A1 (en) | 2015-02-04 |
CA2868627A1 (en) | 2013-10-03 |
EP2831082B1 (en) | 2019-02-20 |
US9695187B2 (en) | 2017-07-04 |
AU2013239290A1 (en) | 2014-10-30 |
AU2013239290B2 (en) | 2017-08-03 |
JP2015512897A (ja) | 2015-04-30 |
WO2013142999A1 (en) | 2013-10-03 |
EP2831082A4 (en) | 2016-01-06 |
US20160152631A1 (en) | 2016-06-02 |
CA2868627C (en) | 2021-02-16 |
CN104334562A (zh) | 2015-02-04 |
US20150065733A1 (en) | 2015-03-05 |
JP6531911B2 (ja) | 2019-06-19 |
US9278979B2 (en) | 2016-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IN2014MN02106A (zh) | ||
GEP20146146B (en) | Pyrrolopyrimidine compounds as inhibitors of cdk4/6 | |
IN2014MN01521A (zh) | ||
IN2014MN02598A (zh) | ||
GEP20207105B (en) | 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives and 1,1,1-trifluoro-4-hydroxybutan-2yl carbamate derivatives as magl inhibitors | |
AU2012214029A8 (en) | Rorgammat inhibitors | |
TN2011000400A1 (en) | Inhibitors of beta-secretase | |
NZ729037A (en) | Carboxylic acid compound, method for preparation thereof, and use thereof | |
PH12014502040A1 (en) | Heterocyclyl compounds | |
MY175854A (en) | Novel quinolone derivatives | |
EA201491362A1 (ru) | Анестезирующие соединения и способы их применения | |
IN2014MN02459A (zh) | ||
IN2014CN04530A (zh) | ||
CR20200286A (es) | DERIVADOS DE DIHIDRO-BENZO-OXAZINA Y DIHIDRO-PIRIDO-OXAZINA (Divisional 2014-0294) | |
MD20160105A2 (ro) | 2-Amino-6-metil-4,4a,5,6-tetrahidropirano[3,4-d][1,3]tiazin-8a(8H)-il-1,3-tiazol-4-il amide | |
PH12013500301A1 (en) | Oxadiazole inhibitors of leukotriene production | |
IN2015DN01119A (zh) | ||
PH12016500885A1 (en) | Novel heterocyclic compounds | |
PH12016500394A1 (en) | Polymorphic form of pyrrole derivative and intermediate thereof | |
IN2012DN02502A (zh) | ||
MX390763B (es) | Compuestos de tetraciclina | |
MX2013008340A (es) | Novedosas 4-amino-n-hidroxi-benzamidas para el tratamiento de cancer. | |
IN2014CN04449A (zh) | ||
WO2013177534A3 (en) | New salicylic acid derivatives, pharmaceutically acceptable salt thereof, composition thereof and method of use thereof | |
UA103329C2 (ru) | Соли соединений-ингибиторов вич |