JP2012519207A5 - - Google Patents

Download PDF

Info

Publication number
JP2012519207A5
JP2012519207A5 JP2011552515A JP2011552515A JP2012519207A5 JP 2012519207 A5 JP2012519207 A5 JP 2012519207A5 JP 2011552515 A JP2011552515 A JP 2011552515A JP 2011552515 A JP2011552515 A JP 2011552515A JP 2012519207 A5 JP2012519207 A5 JP 2012519207A5
Authority
JP
Japan
Prior art keywords
lenalidomide
nitro
solvent system
piperidine
alcohol
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
JP2011552515A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012519207A (ja
JP5727944B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/GB2010/050352 external-priority patent/WO2010100476A2/en
Publication of JP2012519207A publication Critical patent/JP2012519207A/ja
Publication of JP2012519207A5 publication Critical patent/JP2012519207A5/ja
Application granted granted Critical
Publication of JP5727944B2 publication Critical patent/JP5727944B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2011552515A 2009-03-02 2010-03-01 改良プロセス Expired - Fee Related JP5727944B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
IN383/KOL/2009 2009-03-02
IN383KO2009 2009-03-02
IN463KO2009 2009-03-16
IN463/KOL/2009 2009-03-16
PCT/GB2010/050352 WO2010100476A2 (en) 2009-03-02 2010-03-01 Improved process

Publications (3)

Publication Number Publication Date
JP2012519207A JP2012519207A (ja) 2012-08-23
JP2012519207A5 true JP2012519207A5 (enExample) 2013-04-18
JP5727944B2 JP5727944B2 (ja) 2015-06-03

Family

ID=54290149

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011552515A Expired - Fee Related JP5727944B2 (ja) 2009-03-02 2010-03-01 改良プロセス

Country Status (16)

Country Link
US (1) US8946265B2 (enExample)
EP (1) EP2403845B1 (enExample)
JP (1) JP5727944B2 (enExample)
CN (1) CN102414196A (enExample)
AU (1) AU2010220204B2 (enExample)
CA (1) CA2753241C (enExample)
CY (1) CY1115376T1 (enExample)
DK (1) DK2403845T3 (enExample)
ES (1) ES2487215T3 (enExample)
HR (1) HRP20140686T1 (enExample)
NZ (1) NZ595492A (enExample)
PL (1) PL2403845T3 (enExample)
PT (1) PT2403845E (enExample)
SI (1) SI2403845T1 (enExample)
SM (1) SMT201400100B (enExample)
WO (1) WO2010100476A2 (enExample)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA83504C2 (en) 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
TWI475014B (zh) * 2009-09-17 2015-03-01 Scinopharm Taiwan Ltd 固體形態的3-(4-胺基-1-側氧基-1,3-二氫-異吲哚-2-基)-哌啶-2,6-二酮及其製造方法
WO2011064574A1 (en) 2009-11-24 2011-06-03 Generics [Uk] Limited Hplc method for detecting lenalidomide
US8877932B2 (en) 2010-03-08 2014-11-04 Natco Pharma Limited Anhydrous lenalidomide form-I
ES2705244T3 (es) 2010-06-16 2019-03-22 Inflammatory Response Res Inc Levocetirizina y montelukast para el tratamiento de la gripe y del resfriado común
WO2013005229A1 (en) * 2011-07-05 2013-01-10 Hetero Research Foundation Process for lenalidomide
CA2842316A1 (en) 2011-07-19 2013-01-24 Amplio Pharma, Llc Urea cocrystal of 3-(4-amin0-1-0x0-1,3 dihydro-isoindol-2-yl)­piperidine-2,6-dione
CN102838586A (zh) * 2012-09-20 2012-12-26 重庆泰濠制药有限公司 一种制备来那度胺的方法
EP2968309A4 (en) 2013-03-13 2016-08-31 Inflammatory Response Res Inc USE OF LEVOCETRIXIN AND MONTELUKAST IN THE TREATMENT OF VASCULARITY
ES2660494T3 (es) 2013-03-13 2018-03-22 14779507 Uso de levocetirizina y montelukast en el tratamiento de una lesión traumática
CN105228700A (zh) * 2013-03-13 2016-01-06 炎症反应研究公司 左西替利嗪和孟鲁司特在治疗自身免疫病中的用途
WO2014160686A1 (en) * 2013-03-26 2014-10-02 Celgene Corporation Solid forms comprising 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione and a coformer, compositions and methods of use thereof
CN103601717A (zh) * 2013-10-09 2014-02-26 湖南华腾制药有限公司 一种来那度胺的新型制备方法
LV14985B (lv) 2013-10-14 2015-06-20 Latvijas Organiskās Sintēzes Institūts Lenalidomīda iegūšanas process
US20170107193A1 (en) * 2014-04-26 2017-04-20 Shilpa Medicare Limited Crystalline lenalidomide process
WO2016024286A2 (en) * 2014-08-11 2016-02-18 Avra Laboratories Pvt. Ltd. An improved process for synthesis of lenalidomide
ES2733813T3 (es) * 2014-08-19 2019-12-03 Synthon Bv Proceso para preparar una forma cristalina de lenalidomida
JP2017526728A (ja) 2014-09-15 2017-09-14 インフラマトリー・レスポンス・リサーチ・インコーポレイテッド 炎症介在性状態の治療におけるレボセチリジン及びモンテルカスト
EP3393457A1 (en) 2015-12-22 2018-10-31 Synthon B.V. Pharmaceutical composition comprising amorphous lenalidomide and an antioxidant
US10899793B2 (en) 2016-05-27 2021-01-26 Regents Of The University Of Minnesota Melanocortin ligands and methods of use thereof
US11124541B2 (en) 2016-10-18 2021-09-21 Regents Of The University Of Minnesota Chimeric melanocortin ligands and methods of use thereof
EP3687987A4 (en) * 2017-09-27 2021-03-24 Biocon Limited CRYSTALLINE FORMS OF LENALIDOMIDE
WO2019138424A1 (en) * 2018-01-11 2019-07-18 Natco Pharma Limited Stable pharmaceutical compositions comprising lenalidomide
US11332499B2 (en) 2018-08-16 2022-05-17 Regents Of The University Of Minnesota Cyclic peptides and methods of use thereof
CN111196800B (zh) * 2018-11-19 2022-10-11 欣凯医药化工中间体(上海)有限公司 一种制备来那度胺的方法
WO2021236518A1 (en) 2020-05-19 2021-11-25 IRR, Inc. Levocetirizine and montelukast in the treatment of sepsis and symptoms thereof
WO2022144924A1 (en) * 2021-01-04 2022-07-07 Avra Laboratories Pvt. Ltd. An improved process for synthesis of lenalidomide

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6281230B1 (en) 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
US5635517B1 (en) 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
UA83504C2 (en) 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
NZ554068A (en) 2004-09-03 2009-07-31 Celgene Corp Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindo-lines
EP2136896B1 (en) 2007-04-16 2015-01-21 Momenta Pharmaceuticals, Inc. Multi-dimensional chromatographic methods for separating n-glycans
JP2011506950A (ja) 2007-12-14 2011-03-03 ジェネリクス・(ユーケー)・リミテッド クロピドグレルを分析するためのhplc法
KR20100124710A (ko) 2008-03-11 2010-11-29 닥터 레디스 레보러터리즈 리미티드 레날리도미드의 제조
CA2741927A1 (en) 2008-11-03 2010-06-03 Generics [Uk] Limited A crystalline form of lenalidomide and a process for its preparation
WO2011064574A1 (en) 2009-11-24 2011-06-03 Generics [Uk] Limited Hplc method for detecting lenalidomide

Similar Documents

Publication Publication Date Title
CN101253163B (zh) 4-氨基-2-(2,6-二氧哌啶-3-基)异吲哚啉-1,3-二酮化合物的制备方法
JP5426693B2 (ja) アゴメラチンハロゲン化水素複合体及びその製造方法
EP2305667A2 (en) Nilotinib intermediates and preparation thereof
US20120071509A1 (en) process
JP2016512824A5 (enExample)
US20110028508A1 (en) Novel process for the preparation of scopine esters
JP2009542785A5 (enExample)
JP5373996B2 (ja) サクサグリプチン中間体、サクサグリプチン多形及びそれらの調製方法
WO2015163447A1 (ja) 4環性化合物の新規結晶
CN102869650B (zh) 一种厄洛替尼碱的新晶型及其制备方法
CN110891947B (zh) 制备艾乐替尼或其药学上可接受的盐的方法
US10392364B2 (en) Process for synthesis of lenalidomide
CN111315722B (zh) 制备月桂酰阿立哌唑的方法
US9850267B2 (en) Crystalline fosaprepitant dicyclohexylamine salt and its preparation
JP2022060192A5 (enExample)
CN103497175A (zh) 制备来那度胺的方法
KR101032600B1 (ko) 고순도 레바미피드의 제조방법
WO2020053795A2 (en) Process for the preparation of acalabrutinib and its intermediates
CN103298795A (zh) 用于制备来曲唑的纯中间体
WO2014188445A1 (en) PROCESS FOR THE PREPARATION OF (3β)-17-(3-PYRIDINYL)ANDROSTA-5,16-DIEN-3-YL ACETATE AND POLYMORPH THEREOF
CN111808172B (zh) 肺念菌素b0衍生物及其制备方法和用途
EP3679030B1 (en) A process for preparation of triaminopyrimidine compound and intermediates thereof
CN101029045A (zh) 一种制备4-(3-吡啶基)-1h-咪唑-1-丁胺的方法
CN106279112A (zh) 一种克里唑替尼中间体及其制备方法和应用
WO2018021517A1 (ja) 4-アルコキシ-3-トリフルオロメチルベンジルアルコールの製造方法