DE60100750D1 - NEUE KRISTALLINE FORM VON N-[4-[2-(2-AMINO-4,7-DIHYDRO-4-OXO-3H-PYRROLO[2,3-d]-PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMINSÄURE UND VERFAHREN FÜR IHRE HERSTELLUNG - Google Patents

NEUE KRISTALLINE FORM VON N-[4-[2-(2-AMINO-4,7-DIHYDRO-4-OXO-3H-PYRROLO[2,3-d]-PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMINSÄURE UND VERFAHREN FÜR IHRE HERSTELLUNG

Info

Publication number
DE60100750D1
DE60100750D1 DE60100750T DE60100750T DE60100750D1 DE 60100750 D1 DE60100750 D1 DE 60100750D1 DE 60100750 T DE60100750 T DE 60100750T DE 60100750 T DE60100750 T DE 60100750T DE 60100750 D1 DE60100750 D1 DE 60100750D1
Authority
DE
Germany
Prior art keywords
pyrrolo
pyrimidin
dihydro
benzoyl
oxo
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.)
Expired - Lifetime
Application number
DE60100750T
Other languages
English (en)
Other versions
DE60100750T2 (de
Inventor
Christopher Chelius
Marie Reutzel-Edens
Van Den Berghe Snorek
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22679017&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DE60100750(D1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Application granted granted Critical
Publication of DE60100750D1 publication Critical patent/DE60100750D1/de
Publication of DE60100750T2 publication Critical patent/DE60100750T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
DE60100750T 2000-02-25 2001-02-12 NEUE KRISTALLINE FORM VON N-[4-[2-(2-AMINO-4,7-DIHYDRO-4-OXO-3H-PYRROLO[2,3-d]-PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMINSÄURE UND VERFAHREN FÜR IHRE HERSTELLUNG Expired - Lifetime DE60100750T2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US18496400P 2000-02-25 2000-02-25
US184964P 2000-02-25
PCT/US2001/001229 WO2001062760A2 (en) 2000-02-25 2001-02-12 A NOVEL CRYSTALLINE FORM OF N-[4-[2-(2-AMINO-4,7-DIHYDRO-4-OXO-3H-PYRROLO[2,3-d]PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMIC ACID AND PROCESS THEREFOR

Publications (2)

Publication Number Publication Date
DE60100750D1 true DE60100750D1 (de) 2003-10-16
DE60100750T2 DE60100750T2 (de) 2004-07-29

Family

ID=22679017

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60100750T Expired - Lifetime DE60100750T2 (de) 2000-02-25 2001-02-12 NEUE KRISTALLINE FORM VON N-[4-[2-(2-AMINO-4,7-DIHYDRO-4-OXO-3H-PYRROLO[2,3-d]-PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMINSÄURE UND VERFAHREN FÜR IHRE HERSTELLUNG

Country Status (36)

Country Link
US (1) US7138521B2 (de)
EP (1) EP1259513B1 (de)
JP (1) JP4846158B2 (de)
KR (1) KR100744917B1 (de)
CN (1) CN1183135C (de)
AR (1) AR029471A1 (de)
AT (1) ATE249462T1 (de)
AU (1) AU777047B2 (de)
BR (1) BR0108604A (de)
CA (1) CA2400155C (de)
CO (1) CO5261585A1 (de)
CZ (1) CZ303772B6 (de)
DE (1) DE60100750T2 (de)
DK (1) DK1259513T3 (de)
DZ (1) DZ3283A1 (de)
EA (1) EA004684B1 (de)
EG (1) EG24073A (de)
ES (1) ES2206403T3 (de)
HK (1) HK1051856A1 (de)
HR (1) HRP20020701B1 (de)
HU (1) HU229704B1 (de)
IL (2) IL150480A0 (de)
MX (1) MXPA02008242A (de)
MY (1) MY124784A (de)
NO (1) NO323422B1 (de)
NZ (1) NZ519796A (de)
PE (1) PE20011082A1 (de)
PL (1) PL208061B1 (de)
PT (1) PT1259513E (de)
SI (1) SI1259513T1 (de)
SK (1) SK287375B6 (de)
SV (1) SV2002000321A (de)
TW (1) TWI237024B (de)
UA (1) UA72791C2 (de)
WO (1) WO2001062760A2 (de)
ZA (1) ZA200205265B (de)

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CN100364993C (zh) * 2003-05-30 2008-01-30 江苏恒瑞医药股份有限公司 培美曲噻盐及其制备方法
CN100364994C (zh) * 2004-11-25 2008-01-30 重庆医药工业研究院有限责任公司 培美曲塞二钠的一种新晶型及其制备方法
WO2007056135A1 (en) * 2005-11-04 2007-05-18 Merck & Co., Inc. Method of treating cancers with saha and pemetrexed
CN101300015A (zh) * 2005-11-04 2008-11-05 默克公司 使用n-辛二酰苯胺异羟肟酸和厄洛替尼治疗癌症的方法
JP2008543973A (ja) * 2006-08-14 2008-12-04 シコール インコーポレイティド ペメトレキセドの中間体の調製方法
ES2356792T3 (es) * 2006-08-14 2011-04-13 Sicor, Inc. Procedimientos para la preparación de sales farmacéuticamente aceptables liofilizadas de pemetrexed diácido.
EP1934226A2 (de) 2006-08-14 2008-06-25 Sicor, Inc. Pemetrexed-diacid von hoher reinheit und verfahren zu dessen herstellung
ATE490257T1 (de) * 2006-08-14 2010-12-15 Sicor Inc Kristalline formen von pemetrexed-disäure und herstellungsverfahren dafür
CA2667348A1 (en) * 2006-11-03 2008-05-15 University Of Maryland, Baltimore Methods of using saha and bortezomib for treating multiple myeloma
CA2681829A1 (en) 2007-04-03 2008-10-16 Dr. Reddy's Laboratories Ltd. Solid forms of pemetrexed
CN101417998B (zh) 2007-10-24 2012-10-24 重庆医药工业研究院有限责任公司 一种培美曲塞盐的纯化方法
EP2072518A1 (de) * 2007-12-23 2009-06-24 Sun Pharma Advanced Research Company Limited Stabile amorphe Form aus Pemextred Disodium
EP2334685A4 (de) * 2008-09-08 2011-10-26 Reddys Lab Ltd Dr Amorphes pemetrexed-dinatrium
WO2010030598A2 (en) * 2008-09-11 2010-03-18 Dr. Reddy's Laboratories Limited Pharmaceutical formulations comprising pemetrexed
CN101684121B (zh) * 2008-09-22 2013-04-03 重庆医药工业研究院有限责任公司 培美曲塞二酸的新晶型及其制备方法
CN102050825B (zh) * 2009-11-05 2014-12-17 上海创诺制药有限公司 制备培美曲塞二钠2.5水结晶的方法
EP2504341A1 (de) 2009-11-24 2012-10-03 Azad Pharmaceutical Ingredients AG Neue kristalline form von pemetrexed-dinatrium
CN102372719B (zh) * 2010-08-26 2013-10-30 齐鲁制药有限公司 培美曲塞二甲酯对甲苯磺酸盐晶型及其制备方法
KR101069128B1 (ko) * 2011-03-10 2011-09-30 건일제약 주식회사 페메트렉시드 또는 그의 염을 포함하는 항산화제-비함유 주사용 용액 형태의 약학적 제제의 제조방법
US9051322B2 (en) 2011-03-23 2015-06-09 Scinopharm Taiwan, Ltd. Process for the production of a pemetrexed salt
JP5826371B2 (ja) * 2011-03-25 2015-12-02 サイノファーム タイワン リミテッド ペメトレキセド塩の製造方法
ITRM20120398A1 (it) 2012-08-08 2014-02-09 Berlin Chemie Ag Procedimento di sintesi pemetrexed e suo sale di lisina.
CN102911176B (zh) * 2012-10-10 2015-07-22 德州德药制药有限公司 一种培美曲塞二钠的制备方法
WO2014060959A1 (en) * 2012-10-17 2014-04-24 Shilpa Medicare Limited Crystalline pemetrexed dipotassium process
US20150359898A1 (en) 2013-02-06 2015-12-17 Cipla Limited Pemetrexed Complexes and Pharmaceutical Compositions Containing Pemetrexed Complexes
US20160051679A1 (en) 2013-04-12 2016-02-25 Actavis Group Ptc Ehf. Pemetrexed Formulation
KR101485243B1 (ko) * 2013-05-08 2015-01-21 씨제이헬스케어 주식회사 안정화된 페메트렉시드 제제
JP6094388B2 (ja) * 2013-06-07 2017-03-15 ニプロ株式会社 ペメトレキセドを含む注射用組成物
ES2657944T3 (es) 2013-06-14 2018-03-07 Synthon B.V. Sal estable de arginina de pemetrexed y composiciones que la comprenden
JP2016527227A (ja) 2013-07-16 2016-09-08 ドクター レディズ ラボラトリーズ リミテッド ペメトレキセドトロメタミン塩の新規な結晶形
WO2015050230A1 (ja) 2013-10-03 2015-04-09 富士フイルム株式会社 注射液製剤及びその製造方法
NZ630292A (en) * 2013-11-25 2015-02-27 Shilpa Medicare Ltd Process for crystalline pemetrexed dipotassium salt
NZ630299A (en) 2014-06-30 2014-11-28 Shilpa Medicare Ltd Pemetrexed dipotassium formulations
EP3212193A4 (de) * 2014-10-30 2018-08-01 ScinoPharm Taiwan, Ltd. Kristalline formen von pemetrexed-disäure und herstellungsverfahren dafür
CN105566328B (zh) * 2014-11-06 2018-04-24 博瑞生物医药（苏州）股份有限公司 培美曲塞二酸多晶型的制备方法

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NO169490C (no) * 1988-03-24 1992-07-01 Takeda Chemical Industries Ltd Analogifremgangsmaate for fremstilling av terapeutisk aktive pyrrolopyrimidinderivater
KR0162654B1 (ko) * 1989-12-11 1998-11-16 알렌 제이. 시니스갤리 N-(피롤로[2,3-d]피리미딘-3-일아크릴)-글루타민산 유도체
US5416211A (en) * 1992-09-25 1995-05-16 Eli Lilly And Company Process for preparing 5-substituted pyrrolo-[2,3-d]pyrimidines
JP2000516961A (ja) * 1996-08-30 2000-12-19 イーライ・リリー・アンド・カンパニー 非古典的ピロロ［２，３―ｄ］ピリミジン抗葉酸物質
ZA987550B (en) * 1997-09-26 2000-02-21 Lilly Co Eli Processes and intermediates useful to make antifolates.
TR200001220T2 (tr) * 1997-09-26 2001-05-21 Eli Lilly And Company Antifolatlar yapmak için yararlı işlemler ve aramaddeler.
AU6890800A (en) * 1999-08-23 2001-03-19 Eli Lilly And Company A novel crystalline form of disodium n-[4-[2-(2-amino-4,7-dihydro-4-oxo-3h-pyrrolo[2,3-D]- pyrimidin-5-yl)ethyl]benzoyl]-l-glutamic acid salt and processes therefor

Also Published As

Publication number Publication date
SK11862002A3 (sk) 2003-01-09
KR100744917B1 (ko) 2007-08-01
IL150480A (en) 2007-12-03
SI1259513T1 (en) 2003-12-31
HUP0204232A3 (en) 2006-01-30
SK287375B6 (sk) 2010-08-09
CZ303772B6 (cs) 2013-05-02
WO2001062760A2 (en) 2001-08-30
HRP20020701A2 (en) 2003-12-31
PE20011082A1 (es) 2001-10-22
UA72791C2 (uk) 2005-04-15
EA200200905A1 (ru) 2003-02-27
AU3445101A (en) 2001-09-03
KR20020075449A (ko) 2002-10-04
IL150480A0 (en) 2002-12-01
WO2001062760A3 (en) 2001-12-06
EA004684B1 (ru) 2004-06-24
HU229704B1 (en) 2014-05-28
CA2400155A1 (en) 2001-08-30
TWI237024B (en) 2005-08-01
HRP20020701B1 (en) 2011-02-28
AU777047B2 (en) 2004-09-30
NZ519796A (en) 2003-01-31
MXPA02008242A (es) 2002-11-29
DZ3283A1 (fr) 2001-08-30
NO20023974L (no) 2002-08-21
AR029471A1 (es) 2003-07-02
CN1183135C (zh) 2005-01-05
CN1406238A (zh) 2003-03-26
MY124784A (en) 2006-07-31
PT1259513E (pt) 2004-02-27
EP1259513B1 (de) 2003-09-10
CA2400155C (en) 2009-09-15
EG24073A (en) 2008-05-11
US7138521B2 (en) 2006-11-21
DE60100750T2 (de) 2004-07-29
PL356423A1 (en) 2004-06-28
HUP0204232A2 (hu) 2003-04-28
CO5261585A1 (es) 2003-03-31
NO20023974D0 (no) 2002-08-21
CZ20022875A3 (cs) 2003-02-12
PL208061B1 (pl) 2011-03-31
EP1259513A2 (de) 2002-11-27
DK1259513T3 (da) 2004-01-12
JP4846158B2 (ja) 2011-12-28
BR0108604A (pt) 2002-11-19
HK1051856A1 (en) 2003-08-22
SV2002000321A (es) 2002-07-16
JP2003530321A (ja) 2003-10-14
US20030216416A1 (en) 2003-11-20
ES2206403T3 (es) 2004-05-16
ATE249462T1 (de) 2003-09-15
NO323422B1 (no) 2007-04-30
ZA200205265B (en) 2003-11-11

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Representative=s name: KROHER, STROBEL RECHTS- UND PATENTANWAELTE, 80336

8328 Change in the person/name/address of the agent

Representative=s name: DR. SCHOEN & PARTNER, 80336 MUENCHEN