PL2477973T3 - Sposób wytwarzania krystalicznej formy lenalidomidu - Google Patents

Sposób wytwarzania krystalicznej formy lenalidomidu

Info

Publication number
PL2477973T3
PL2477973T3 PL10760094T PL10760094T PL2477973T3 PL 2477973 T3 PL2477973 T3 PL 2477973T3 PL 10760094 T PL10760094 T PL 10760094T PL 10760094 T PL10760094 T PL 10760094T PL 2477973 T3 PL2477973 T3 PL 2477973T3
Authority
PL
Poland
Prior art keywords
lenalidomide
preparation
crystalline form
crystalline
Prior art date
Application number
PL10760094T
Other languages
English (en)
Inventor
Saridi Madhava Dileep Kumar
Munish Kapoor
Swargam Sathyanarayana
Rajesh Kumar Thaper
Mohan Prasad
Original Assignee
Ranbaxy Laboratories Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ranbaxy Laboratories Ltd filed Critical Ranbaxy Laboratories Ltd
Publication of PL2477973T3 publication Critical patent/PL2477973T3/pl

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
PL10760094T 2009-09-16 2010-09-16 Sposób wytwarzania krystalicznej formy lenalidomidu PL2477973T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN1930DE2009 2009-09-16
PCT/IB2010/054187 WO2011033468A1 (en) 2009-09-16 2010-09-16 Process for the preparation of a crystalline form of lenalidomid
EP10760094.2A EP2477973B1 (en) 2009-09-16 2010-09-16 Process for the preparation of a crystalline form of lenalidomide

Publications (1)

Publication Number Publication Date
PL2477973T3 true PL2477973T3 (pl) 2015-04-30

Family

ID=43030839

Family Applications (1)

Application Number Title Priority Date Filing Date
PL10760094T PL2477973T3 (pl) 2009-09-16 2010-09-16 Sposób wytwarzania krystalicznej formy lenalidomidu

Country Status (4)

Country Link
US (1) US20120220777A1 (pl)
EP (1) EP2477973B1 (pl)
PL (1) PL2477973T3 (pl)
WO (1) WO2011033468A1 (pl)

Families Citing this family (5)

* 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
EP3744318A1 (en) 2015-08-27 2020-12-02 Grindeks, A Joint Stock Company Pharmaceutical composition capable of the incorporation of lenalidomide in various crystalline modifications
RU2616976C1 (ru) * 2016-04-07 2017-04-19 Олег Ростиславович Михайлов Кристаллическая β-модификация 3-(4-амино-1-оксо-1,3-дигидро-2Н-изоиндол-2-ил)-пиперидин-2,6-диона, способ её получения и фармацевтическая композиция на её основе
CN106957299B (zh) * 2017-03-31 2021-02-26 常州制药厂有限公司 一种来那度胺制备方法

Family Cites Families (4)

* 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
EP1797068B1 (en) * 2004-09-03 2013-10-09 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines

Also Published As

Publication number Publication date
EP2477973A1 (en) 2012-07-25
EP2477973B1 (en) 2014-08-27
US20120220777A1 (en) 2012-08-30
WO2011033468A1 (en) 2011-03-24

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