CY1107198T1 - Μεθοδος παραγωγης κρυσταλλου - Google Patents

Μεθοδος παραγωγης κρυσταλλου

Info

Publication number
CY1107198T1
CY1107198T1 CY20081100182T CY081100182T CY1107198T1 CY 1107198 T1 CY1107198 T1 CY 1107198T1 CY 20081100182 T CY20081100182 T CY 20081100182T CY 081100182 T CY081100182 T CY 081100182T CY 1107198 T1 CY1107198 T1 CY 1107198T1
Authority
CY
Cyprus
Prior art keywords
methyl
trifluoroethoxy
sulfinyl
benzimidazole
pyridyl
Prior art date
Application number
CY20081100182T
Other languages
English (en)
Inventor
Hideo Hashimoto
Hideaki Maruyama
Original Assignee
Takeda Pharmaceutical Company Limited
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 Takeda Pharmaceutical Company Limited filed Critical Takeda Pharmaceutical Company Limited
Publication of CY1107198T1 publication Critical patent/CY1107198T1/el

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B7/00Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Η παρούσα εφεύρεση αναφέρεται σε μία μέθοδο παραγωγής ενός κρυστάλλου της (R)-2-[[[3-μεθυλ-4-(2,2,2-τριφθοροαιθοξυ)-2-πυριδυλ]μεθυλ]σουλφινυλ]βενζιμιδαζόλης ˙ n'Η2O (όπου n' είναι περίπου 0 έως περίπου 0,1) ή ενός άλατος αυτής, η οποία χαρακτηριστικά περιλαμβάνει την κρυστάλλωση από ένα διάλυμα ή εναιώρημα οργανικού διαλύτη στο οποίο η (R)-2-[[[3-μεθυλ-4-(2,2,2-τριφθοροαιθοξυ)-2-πυριδυλ] μεθυλ] σουλφινυλ] βενζιμιδα-ζόλη ˙ nΗ2O (όπου n είναι περίπου 0,1 έως περίπου 1,0) ή ένα άλας αυτής έχει διαλυθεί ή τεθεί σε εναιώρηση, και παρόμοια, και παρέχει μία πρακτική μέθοδο για την αποδοτική παραγωγή ενός οπτικά ενεργού παραγώγου του σουλφοξειδίου που έχει εξαιρετικά υψηλή περίσσεια εναντιομερούς με υψηλή απόδοση σε μεγάλη βιομηχανική κλίμακα.
CY20081100182T 2000-05-15 2008-02-14 Μεθοδος παραγωγης κρυσταλλου CY1107198T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2000141670 2000-05-15
EP01930131A EP1293507B1 (en) 2000-05-15 2001-05-15 Process for producing crystal

Publications (1)

Publication Number Publication Date
CY1107198T1 true CY1107198T1 (el) 2012-11-21

Family

ID=18648753

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20081100182T CY1107198T1 (el) 2000-05-15 2008-02-14 Μεθοδος παραγωγης κρυσταλλου

Country Status (12)

Country Link
US (4) US7169799B2 (el)
EP (3) EP1293507B1 (el)
KR (2) KR101035534B1 (el)
CN (2) CN100562318C (el)
AU (1) AU2001256732A1 (el)
CA (3) CA2409044C (el)
CY (1) CY1107198T1 (el)
DE (1) DE60131649T2 (el)
DK (1) DK1293507T3 (el)
ES (3) ES2511774T3 (el)
PT (1) PT1293507E (el)
WO (1) WO2001087874A1 (el)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2511774T3 (es) * 2000-05-15 2014-10-23 Takeda Pharmaceutical Company Limited Formas cristalinas de (R)-lansoprazol
CA2775616C (en) * 2000-08-04 2013-09-17 Takeda Pharmaceutical Company Limited Salts of benzimidazole compound and application thereof
US7285668B2 (en) 2000-12-01 2007-10-23 Takeda Pharmaceutical Company Limited Process for the crystallization of (R)- or (S)-lansoprazole
AU2003273000A1 (en) * 2002-10-16 2004-05-04 Takeda Pharmaceutical Company Limited Stable solid preparations
CA2510849A1 (en) * 2002-12-19 2004-07-08 Teva Pharmaceutical Industries Ltd Solid states of pantoprazole sodium, processes for preparing them and processes for preparing known pantoprazole sodium hydrates
EP1604665B1 (en) * 2003-03-10 2011-05-11 Eisai R&D Management Co., Ltd. C-kit kinase inhibitor
SE0400410D0 (sv) * 2004-02-20 2004-02-20 Astrazeneca Ab New compounds
CA2570916C (en) 2004-06-16 2013-06-11 Tap Pharmaceutical Products, Inc. Pulsed release dosage form of a ppi
WO2006101062A1 (ja) * 2005-03-22 2006-09-28 Daiichi Sankyo Company, Limited 1-アルキルピロリジン構造を有するカルバペネム誘導体の製造方法
JPWO2006121151A1 (ja) * 2005-05-13 2008-12-18 第一三共株式会社 1−メチルカルバペネム化合物の結晶
WO2006132217A1 (ja) * 2005-06-07 2006-12-14 Takeda Pharmaceutical Company Limited ベンズイミダゾール化合物の塩の結晶
CN101389316A (zh) 2005-12-28 2009-03-18 武田药品工业株式会社 控制释放固体制剂
JP5366558B2 (ja) 2006-12-28 2013-12-11 武田薬品工業株式会社 口腔内崩壊性固形製剤
CN102014638A (zh) * 2007-10-12 2011-04-13 武田制药北美公司 与食物摄入无关的治疗胃肠病症的方法
US8214093B2 (en) * 2007-11-04 2012-07-03 GM Global Technology Operations LLC Method and apparatus to prioritize transmission output torque and input acceleration for a hybrid powertrain system
JP2011507977A (ja) * 2007-12-31 2011-03-10 武田薬品工業株式会社 (r)−2−[[[3−メチル−4−(2,2,2−トリフルオロエトキシ)−2−ピリジニル]メチル]スルフィニル]−1h−ベンズイミダゾールの溶媒和物結晶形
JP2011513202A (ja) 2008-03-10 2011-04-28 武田薬品工業株式会社 ベンズイミダゾール化合物の結晶
WO2010039885A2 (en) * 2008-09-30 2010-04-08 Teva Pharmaceutical Industries Ltd. Crystalline forms of dexlansoprazole
IT1391776B1 (it) 2008-11-18 2012-01-27 Dipharma Francis Srl Procedimento per la preparazione di dexlansoprazolo
IT1392813B1 (it) * 2009-02-06 2012-03-23 Dipharma Francis Srl Forme cristalline di dexlansoprazolo
US20110009637A1 (en) * 2009-02-10 2011-01-13 Dario Braga Crystals of Dexlansoprazole
WO2011004387A2 (en) 2009-06-18 2011-01-13 Matrix Laboratories Ltd Process for the preparation of dexlansoprazole polymorphic forms
IT1395118B1 (it) 2009-07-29 2012-09-05 Dipharma Francis Srl Procedimento per la preparazione di dexlansoprazolo cristallino
US20130197232A1 (en) * 2010-01-29 2013-08-01 Ranbaxy Laboratories Limited Process for the preparation of crystalline forms of dexlansoprazole
CA2795056C (en) 2010-03-31 2015-03-24 Ranbaxy Laboratories Limited Salts of dexlansoprazole and their preparation
WO2011121548A1 (en) 2010-03-31 2011-10-06 Ranbaxy Laboratories Limited Process for the preparation of dexlansoprazole
KR101908748B1 (ko) 2010-12-03 2018-10-16 다케다 야쿠힌 고교 가부시키가이샤 구강내 붕괴정
SG10201602311XA (en) 2010-12-27 2016-04-28 Takeda Pharmaceutical Orally disintegrating tablet
WO2012104805A1 (en) 2011-02-01 2012-08-09 Ranbaxy Laboratories Limited Process for the preparation of dexlansoprazole
WO2012176140A1 (en) 2011-06-21 2012-12-27 Ranbaxy Laboratories Limited Process for the preparation of dexlansoprazole
CN102234265B (zh) * 2011-08-08 2013-11-20 天津市汉康医药生物技术有限公司 兰索拉唑化合物
EP2785331B1 (en) 2011-11-30 2015-11-18 Takeda Pharmaceutical Company Limited Dry coated tablet
WO2013140120A1 (en) 2012-03-22 2013-09-26 Cipla Limited Glycerol solvate forms of (r) - 2 - [ [ [3 -methyl -4 (2,2, 2 - trifluoroethoxy) pyridin- 2 - yl] methyl] sulphinyl] - 1h - ben zimidazole
WO2013179194A1 (en) 2012-05-31 2013-12-05 Ranbaxy Laboratories Limited Process for the preparation of crystalline dexlansoprazole
CN105392486A (zh) 2013-05-21 2016-03-09 武田药品工业株式会社 口腔崩解片
DE102014109120B4 (de) 2014-06-30 2017-04-06 Krohne Messtechnik Gmbh Mikrowellenmodul
CN109111430B (zh) * 2017-06-26 2022-09-30 江苏豪森药业集团有限公司 一种右兰索拉唑晶型a及其制备方法

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6150978A (ja) 1984-08-16 1986-03-13 Takeda Chem Ind Ltd ピリジン誘導体およびその製造法
DK171989B1 (da) * 1987-08-04 1997-09-08 Takeda Chemical Industries Ltd Fremgangsmåde til fremstilling af 2-(2-pyridylmethylsulfinyl)-benzimidazoler
DE4035455A1 (de) 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
SE504459C2 (sv) 1994-07-15 1997-02-17 Astra Ab Förfarande för framställning av substituerade sulfoxider
GB9423968D0 (en) 1994-11-28 1995-01-11 Astra Ab Resolution
HRP960232A2 (en) 1995-07-03 1998-02-28 Astra Ab A process for the optical purification of compounds
TW385306B (en) * 1996-11-14 2000-03-21 Takeda Chemical Industries Ltd Method for producing crystals of benzimidazole derivatives
SE510666C2 (sv) 1996-12-20 1999-06-14 Astra Ab Nya Kristallmodifikationer
JP3929607B2 (ja) 1997-07-23 2007-06-13 エーザイ・アール・アンド・ディー・マネジメント株式会社 ピリジン誘導体の製造方法
EP1056456A4 (en) 1998-01-30 2006-10-25 Sepracor Inc R-LANSOPRAZOL COMPOSITIONS AND TREATMENTS THEREFOR
WO1999038512A1 (en) 1998-01-30 1999-08-05 Sepracor Inc. S-lansoprazole compositions and methods
CN1087739C (zh) 1998-12-28 2002-07-17 中国科学院成都有机化学研究所 光学纯的苯并咪唑类抗消化性溃疡药物的包结拆分制备法
TWI275587B (en) * 1999-06-17 2007-03-11 Takeda Chemical Industries Ltd A crystal of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole
DE60020967T2 (de) 1999-06-30 2006-05-04 Takeda Pharmaceutical Co. Ltd. Kristalle von lansoprazole
ES2511774T3 (es) * 2000-05-15 2014-10-23 Takeda Pharmaceutical Company Limited Formas cristalinas de (R)-lansoprazol
US7285668B2 (en) * 2000-12-01 2007-10-23 Takeda Pharmaceutical Company Limited Process for the crystallization of (R)- or (S)-lansoprazole
EP1945623A2 (en) * 2005-11-10 2008-07-23 Wyeth a Corporation of the State of Delaware Polymorphs of 5-cyclopropyl-2-(4-fluorophenyl)-6-[(2-hydroxyethyl)(methylsulfonyl) amino]-n-methyl-1-benzofuran-3-carboxamide and methods of making the same

Also Published As

Publication number Publication date
ES2293988T3 (es) 2008-04-01
DE60131649D1 (de) 2008-01-10
EP2281821A1 (en) 2011-02-09
KR20090076980A (ko) 2009-07-13
CA2762960C (en) 2014-07-22
AU2001256732A1 (en) 2001-11-26
PT1293507E (pt) 2008-01-16
KR101035534B1 (ko) 2011-05-23
ES2511774T3 (es) 2014-10-23
KR20080067713A (ko) 2008-07-21
EP1897877A2 (en) 2008-03-12
US20070004779A1 (en) 2007-01-04
EP1293507B1 (en) 2007-11-28
CA2762960A1 (en) 2001-11-22
EP1897877B1 (en) 2014-09-24
US7169799B2 (en) 2007-01-30
CA2701704A1 (en) 2001-11-22
US20100004458A1 (en) 2010-01-07
CN1280287C (zh) 2006-10-18
CA2701704C (en) 2011-09-06
DE60131649T2 (de) 2008-10-30
WO2001087874A1 (fr) 2001-11-22
CN1437592A (zh) 2003-08-20
CA2409044A1 (en) 2002-11-14
US8212046B2 (en) 2012-07-03
ES2521690T3 (es) 2014-11-13
EP1293507A4 (en) 2005-09-07
US20110257405A1 (en) 2011-10-20
EP2281821B1 (en) 2014-10-22
EP1293507A1 (en) 2003-03-19
EP1897877A3 (en) 2008-12-10
US7994332B2 (en) 2011-08-09
DK1293507T3 (da) 2007-12-27
US7569696B2 (en) 2009-08-04
CA2409044C (en) 2013-02-19
US20030153766A1 (en) 2003-08-14
CN100562318C (zh) 2009-11-25
CN1803137A (zh) 2006-07-19

Similar Documents

Publication Publication Date Title
CY1107198T1 (el) Μεθοδος παραγωγης κρυσταλλου
DE69226822D1 (de) Diastereomeres Salz von optisch aktiver Chinolinmevalonsäure
DE60020967D1 (de) Kristalle von lansoprazole
NO20016087D0 (no) Benzimidazolforbindelsekrystall
YU99291A (sh) Postupak za sintezu omeprazola
ATE406362T1 (de) Verfahren zur herstellung von optisch aktiven derivaten von 2-(2- pyridylmethylsulfinyl)benzimidazol über einen einschlusskomplex mit 1,1'-binaphthalin-2, 2'- diol
CY1114058T1 (el) Μεθοδος παρασκευης οπτικως καθαρων δραστικων ενωσεων
ITMI921203A1 (it) Derivati di s-triazina come agenti fotostabilizzanti
EA200300211A1 (ru) Азабициклические соединения, способ их получения и их применение в качестве лекарственных средств, в частности в качестве антибактериальных средств
ATE266010T1 (de) Amphotere optische aufheller, ihre wässerigen lösungen, verfahren zu ihrer herstellung und ihre verwendung
BR0211101B1 (pt) Processo melhorado para preparação de compostos tipo benzimidazol
PE20091387A1 (es) Proceso de preparacion de derivados de tetrazol-5-il-bifenilo
ATE347555T1 (de) 6-aminomorphinanderivate, herstellungsverfahren dafür und deren verwendung
NO20024858D0 (no) Fremgangsmåte for fremstilling av derivater av [[(substituert pyridyl)metyl]tio]benzimidazol
CY1105781T1 (el) Μεθοδος για την παρασκευη παραγωγων αμινο-πυρρολιδινης
DE60316791D1 (de) Verfahren zur aufreinigung von lanzoprazol
PT1106698E (pt) Processo para a producao e para a recuperacao do eritritol a partir de um meio de cultura contendo o mesmo
BR0314461A (pt) Processo para a preparação de derivado de 2-aminometilpiridina
ES2104987T3 (es) Derivados de eteres milbemicina, su preparacion y su aplicacion terapeutica y agroquimica.
ES2149281T3 (es) Derivado opticamente activo de imidazolidinona y su proceso de fabricacion.
BRPI0013751B8 (pt) processo para produção de derivados de ácido naftiridina-3-carboxílico.
HUP9801117A2 (hu) Eljárás optikailag aktív aminszármazékok előállítására
ATE321033T1 (de) Verfahren zur herstellung von substituierten alkylaminen oder salzen davon
ATE546432T1 (de) Verfahren zur herstellung von 2- aminomethylpyridin-derivate
ATE286048T1 (de) Verfahren zur herstellung von carbostyril- derivaten