JP2011507977A5 - - Google Patents

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Publication number
JP2011507977A5
JP2011507977A5 JP2010541519A JP2010541519A JP2011507977A5 JP 2011507977 A5 JP2011507977 A5 JP 2011507977A5 JP 2010541519 A JP2010541519 A JP 2010541519A JP 2010541519 A JP2010541519 A JP 2010541519A JP 2011507977 A5 JP2011507977 A5 JP 2011507977A5
Authority
JP
Japan
Prior art keywords
methyl
powder
ray diffraction
trifluoroethoxy
sulfinyl
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.)
Abandoned
Application number
JP2010541519A
Other languages
English (en)
Japanese (ja)
Other versions
JP2011507977A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/088534 external-priority patent/WO2009088857A1/en
Publication of JP2011507977A publication Critical patent/JP2011507977A/ja
Publication of JP2011507977A5 publication Critical patent/JP2011507977A5/ja
Abandoned legal-status Critical Current

Links

JP2010541519A 2007-12-31 2008-12-30 (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 Abandoned JP2011507977A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1802107P 2007-12-31 2007-12-31
PCT/US2008/088534 WO2009088857A1 (en) 2007-12-31 2008-12-30 Crystalline solvated forms of (r) -2- [ [ [3-methyl-4- (2, 2, 2-trifluoroethoxy) -2-pyridinyl] methyl] sulfinyl] -1h-benz imidazole

Publications (2)

Publication Number Publication Date
JP2011507977A JP2011507977A (ja) 2011-03-10
JP2011507977A5 true JP2011507977A5 (enExample) 2012-02-09

Family

ID=40364382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010541519A Abandoned JP2011507977A (ja) 2007-12-31 2008-12-30 (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

Country Status (5)

Country Link
US (1) US20100286400A1 (enExample)
EP (3) EP2292612A3 (enExample)
JP (1) JP2011507977A (enExample)
CA (2) CA2738458A1 (enExample)
WO (1) WO2009088857A1 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ588379A (en) 2008-03-10 2012-07-27 Takeda Pharmaceutical Crystal of benzimidazole compound
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
WO2010095144A2 (en) * 2009-02-04 2010-08-26 Msn Laboratories Limited Process for the preparation of proton pump inhibitors
IT1392813B1 (it) * 2009-02-06 2012-03-23 Dipharma Francis Srl Forme cristalline di dexlansoprazolo
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
WO2011020189A1 (en) * 2009-08-19 2011-02-24 Apotex Pharmachem Inc. Forms of dexlansoprazole and processes for the preparation thereof
WO2011098938A1 (en) * 2010-02-11 2011-08-18 Orchid Chemicals And Pharmaceuticals Limited Novel solvate of dexlansoprazole
WO2011139414A2 (en) * 2010-04-27 2011-11-10 Dr. Reddy's Laboratories Ltd. Dexlansoprazole polymorphic forms
US20140357870A1 (en) * 2011-06-21 2014-12-04 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
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
CN104177333A (zh) * 2013-05-24 2014-12-03 四川海思科制药有限公司 一种理化性质稳定的(r)-2-[[[3-甲基-4-(2,2,2-三氟乙氧基)-2-吡啶基]甲基]亚磺酰基]-1h-苯并咪唑
CN104650035A (zh) * 2013-11-25 2015-05-27 天津市汉康医药生物技术有限公司 右兰索拉唑倍半水合物化合物
WO2016174664A1 (en) 2015-04-29 2016-11-03 Dexcel Pharma Technologies Ltd. Orally disintegrating compositions
US10076494B2 (en) 2016-06-16 2018-09-18 Dexcel Pharma Technologies Ltd. Stable orally disintegrating pharmaceutical compositions
IT201700050223A1 (it) * 2017-05-09 2018-11-09 Dipharma Francis Srl Procedimento per la preparazione di dexlansoprazolo cristallino
PL3495422T3 (pl) 2017-12-05 2021-05-31 Borealis Ag Kompozycja polipropylenowa wzmocniona włóknami

Family Cites Families (11)

* 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
TW385306B (en) * 1996-11-14 2000-03-21 Takeda Chemical Industries Ltd Method for producing crystals of benzimidazole derivatives
JP3283252B2 (ja) 1999-06-17 2002-05-20 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
TWI289557B (en) * 1999-06-17 2007-11-11 Takeda Chemical Industries Ltd A crystal of a hydrate of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole
JP3374314B2 (ja) 2000-05-15 2003-02-04 武田薬品工業株式会社 結晶の製造法
CN100562318C (zh) * 2000-05-15 2009-11-25 武田药品工业株式会社 晶体的制备方法
JP4160293B2 (ja) 2000-12-01 2008-10-01 武田薬品工業株式会社 結晶の製造法
US6627646B2 (en) * 2001-07-17 2003-09-30 Sepracor Inc. Norastemizole polymorphs
AU2003273000A1 (en) * 2002-10-16 2004-05-04 Takeda Pharmaceutical Company Limited Stable solid preparations
MY148805A (en) 2002-10-16 2013-05-31 Takeda Pharmaceutical Controlled release preparation
ITMI20062481A1 (it) * 2006-12-22 2008-06-23 Recordati Chem Pharm Processo per la preparazione di lansoprazolo forma i microcristallino

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