JP2010539237A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010539237A5 JP2010539237A5 JP2010525832A JP2010525832A JP2010539237A5 JP 2010539237 A5 JP2010539237 A5 JP 2010539237A5 JP 2010525832 A JP2010525832 A JP 2010525832A JP 2010525832 A JP2010525832 A JP 2010525832A JP 2010539237 A5 JP2010539237 A5 JP 2010539237A5
- Authority
- JP
- Japan
- Prior art keywords
- solid
- hcl salt
- salt
- xrpd pattern
- hcl
- 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
Links
- 239000007787 solid Substances 0.000 claims 23
- 150000003840 hydrochlorides Chemical class 0.000 claims 13
- 238000000634 powder X-ray diffraction Methods 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 4
- CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 4
- 208000035473 Communicable disease Diseases 0.000 claims 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 3
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 2
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 2
- -1 edisylate Chemical compound 0.000 claims 2
- 239000012535 impurity Substances 0.000 claims 2
- 208000032839 leukemia Diseases 0.000 claims 2
- 201000000050 myeloid neoplasm Diseases 0.000 claims 2
- 201000009030 Carcinoma Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- CVWXJKQAOSCOAB-UHFFFAOYSA-N CC(C)(C)c1cc(NC(Nc(cc2)ccc2-c2c[n](c(ccc(OCCN3CCOCC3)c3)c3[s]3)c3n2)=O)n[o]1 Chemical compound CC(C)(C)c1cc(NC(Nc(cc2)ccc2-c2c[n](c(ccc(OCCN3CCOCC3)c3)c3[s]3)c3n2)=O)n[o]1 CVWXJKQAOSCOAB-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99463507P | 2007-09-19 | 2007-09-19 | |
| US60/994,635 | 2007-09-19 | ||
| PCT/US2008/010884 WO2009038757A2 (en) | 2007-09-19 | 2008-09-19 | Solid forms comprising n-(5-tert-butyl-isoxazol-3-yl)-n'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea, compositions thereof, and uses therewith |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010539237A JP2010539237A (ja) | 2010-12-16 |
| JP2010539237A5 true JP2010539237A5 (enExample) | 2011-10-27 |
| JP5462168B2 JP5462168B2 (ja) | 2014-04-02 |
Family
ID=40468693
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010525832A Active JP5462168B2 (ja) | 2007-09-19 | 2008-09-19 | Ｎ−（５−ｔｅｒｔ−ブチル−イソオキサゾール−３−イル）−Ｎ’−｛４−［７−（２−モルホリン−４−イル−エトキシ）イミダゾ［２，１−ｂ］［１，３］ベンゾチアゾール−２−イル］フェニル｝ウレアを含む固形、その組成物、及びその用途 |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US8883783B2 (enExample) |
| EP (1) | EP2201018B1 (enExample) |
| JP (1) | JP5462168B2 (enExample) |
| KR (2) | KR20150104231A (enExample) |
| CN (1) | CN101868465B (enExample) |
| AR (1) | AR068528A1 (enExample) |
| AU (1) | AU2008302744B2 (enExample) |
| BR (1) | BRPI0816904B8 (enExample) |
| CA (1) | CA2696776C (enExample) |
| CY (1) | CY1117583T1 (enExample) |
| DK (1) | DK2201018T3 (enExample) |
| ES (1) | ES2573292T3 (enExample) |
| HR (1) | HRP20160520T1 (enExample) |
| HU (1) | HUE027982T2 (enExample) |
| IL (1) | IL203926A (enExample) |
| MX (1) | MX2010002295A (enExample) |
| PL (1) | PL2201018T3 (enExample) |
| SI (1) | SI2201018T1 (enExample) |
| TW (1) | TWI437988B (enExample) |
| WO (1) | WO2009038757A2 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101449057B1 (ko) | 2006-03-17 | 2014-10-10 | 암비트 바이오사이언시즈 코포레이션 | 질환 치료용 이미다졸로티아졸 화합물 |
| BRPI0816904B8 (pt) | 2007-09-19 | 2021-12-07 | Ambit Biosciences Corp | Forma cristalna b da forma sólida do sal de bis-hcl, composição farmacêutica, e, uso de uma forma sólida |
| AU2008325141B2 (en) * | 2007-11-08 | 2014-03-20 | Ambit Biosciences Corp. | Methods of administering N-(5-tert-butyl-isoxazol-3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea to treat proliferative disease |
| CN102438588B (zh) | 2009-03-23 | 2015-04-01 | 埃姆比特生物科学公司 | 使用联合治疗法治疗疾病的方法 |
| SMT202000092T1 (it) | 2009-05-14 | 2020-05-08 | Ambit Biosciences Corp | Formulazione essiccata a spruzzo o liofilizzata di ac220 |
| CN104447801A (zh) | 2009-11-05 | 2015-03-25 | 埃姆比特生物科学公司 | 用于制备咪唑并[2,1-b][1,3]苯并噻唑衍生物的方法 |
| WO2011056764A1 (en) | 2009-11-05 | 2011-05-12 | Ambit Biosciences Corp. | Isotopically enriched or fluorinated imidazo[2,1-b][1,3]benzothiazoles |
| CN103172648B (zh) * | 2011-12-20 | 2016-05-25 | 上海迪诺医药科技有限公司 | 三杂环衍生物、制备方法及应用 |
| JP6116847B2 (ja) | 2012-10-01 | 2017-04-19 | アムビト バイオサイエンシス コーポレーションＡｍｂｉｔ Ｂｉｏｓｃｉｅｎｃｅｓ Ｃｏｒｐｏｒａｔｉｏｎ | シクロデキストリンとの混合体を含有する錠剤 |
| CN104513258B (zh) * | 2013-09-26 | 2018-04-03 | 广东东阳光药业有限公司 | 取代脲衍生物及其在药物中的应用 |
| JP6564449B2 (ja) | 2015-02-20 | 2019-08-21 | 第一三共株式会社 | がんの併用治療法 |
| AU2018299536B2 (en) * | 2017-07-13 | 2022-06-02 | Sunshine Lake Pharma Co., Ltd. | Salt of substituted urea derivative and use thereof in medicine |
| US11634442B2 (en) * | 2017-07-18 | 2023-04-25 | Basf Se | Methods for the purification of L-glufosinate |
| CN110763544A (zh) * | 2019-09-20 | 2020-02-07 | 南京聚谱检测科技有限公司 | 一种激光剥蚀样品制靶用快干可精磨粘合剂 |
| CN111413421A (zh) * | 2020-02-20 | 2020-07-14 | 广东电科院能源技术有限责任公司 | 污泥燃烧后灰尘中氯离子含量的测试方法、控制方法 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL129432C (enExample) | 1964-02-29 | |||
| NL129626C (enExample) | 1964-04-08 | |||
| US3210370A (en) | 1964-06-22 | 1965-10-05 | Upjohn Co | Process for preparing 2, 2'-methylene-bisareneimiazoles |
| FR2463774A1 (fr) | 1979-08-21 | 1981-02-27 | Yamanouchi Pharma Co Ltd | Derives du 2-phenylimidazo(2,1-b)benzothiazole |
| US4354970A (en) | 1980-03-07 | 1982-10-19 | Eastman Kodak Company | Indoline coupled isothiazole azo dyes |
| JPS56138196A (en) | 1980-03-29 | 1981-10-28 | Yamanouchi Pharmaceut Co Ltd | Imidazo (2,1-b)benzothiazole derivative |
| JPS5740492A (en) | 1980-08-22 | 1982-03-06 | Yamanouchi Pharmaceut Co Ltd | Novel 2-phenylimidazo 2,1-b benzothiazole derivative |
| JPS57149288A (en) | 1981-03-12 | 1982-09-14 | Yamanouchi Pharmaceut Co Ltd | Imidazo(2,1-b)benzothiazole derivative |
| US4464384A (en) | 1981-12-23 | 1984-08-07 | Yamanouchi Pharmaceutical Co., Ltd. | 2-Phenylimidazo[2,1-b]benzothiazole compounds, salts thereof, process of producing them, and pharmaceutical compositions containing them |
| JPS58109491A (ja) * | 1981-12-23 | 1983-06-29 | Yamanouchi Pharmaceut Co Ltd | ２−フエニルイミダゾ〃２，１−ｂ「あ」ベンゾチアゾ−ル誘導体 |
| US5236952A (en) | 1986-03-11 | 1993-08-17 | Hoffmann-La Roche Inc. | Catechol derivatives |
| US4880824A (en) | 1987-09-21 | 1989-11-14 | Ortho Pharmaceutical Corporation | Phenyl and benzoyl substituted imidazo-fused heterocyclic calcium channel blockers |
| EP0524055A1 (fr) | 1991-07-19 | 1993-01-20 | Synthelabo | Dérivés d'imidazo[2,1-b]benzothiazole-3-acétamide, leur préparation et leur application en thérapeutique |
| JPH05107705A (ja) | 1991-10-17 | 1993-04-30 | Konica Corp | 新規な写真用カプラー |
| ES2126636T3 (es) | 1992-05-19 | 1999-04-01 | Adir | Derivados del bencimidazol con actividad antidiabetica y antiagregante plaquetaria. |
| FR2699920B1 (fr) | 1992-12-24 | 1995-02-10 | Synthelabo | Dérivés d'imidazo [2,1-b] benzothiazole-3-acétamide, leur préparation et leur application en thérapeutique. |
| EP0607076A1 (fr) | 1993-01-15 | 1994-07-20 | Synthelabo | Dérivés de 9h-imidazo 1,2-a benzimidazole-3-acétamide à activité GABA |
| FR2700546B1 (fr) | 1993-01-15 | 1995-02-17 | Synthelabo | Dérivés d'imidazo[2,1-b]benzoxazole-3-acétamide, leur préparation et leur application en thérapeutique. |
| JPH07291976A (ja) | 1994-04-27 | 1995-11-07 | Otsuka Pharmaceut Factory Inc | イミダゾ〔２，１−ｂ〕チアゾール誘導体 |
| FR2722501B1 (fr) | 1994-07-13 | 1996-08-09 | Synthelabo | Derives de 9h-imidazo(1,2-a)benzimidazole-3-acetamide, leur preparation et leur application en therapeutique |
| JP3178843B2 (ja) | 1995-03-13 | 2001-06-25 | 日研化学株式会社 | イミダゾチアゾール化合物 |
| AU3783497A (en) | 1996-08-09 | 1998-03-06 | Yamanouchi Pharmaceutical Co., Ltd. | Metabotropic glutamate receptor agonists |
| US6127387A (en) | 1996-12-10 | 2000-10-03 | Thomas Jefferson University | Use of CD4-binding small molecules to inhibit immune responses |
| FR2759698B1 (fr) | 1997-02-20 | 1999-03-19 | Synthelabo | Derives de 1,4-diphenylimidazole-5-acetamide, leur preparation et leur application en therapeutique |
| JPH11106340A (ja) | 1997-10-02 | 1999-04-20 | Sumitomo Pharmaceut Co Ltd | Ｓｔａｔ６活性化阻害剤 |
| JP4437270B2 (ja) | 1997-12-22 | 2010-03-24 | バイエル コーポレイション | 置換複素環式尿素を用いたｒａｆキナーゼの阻害 |
| DE19805117A1 (de) | 1998-02-09 | 1999-08-12 | Bayer Ag | Neue Oxazolidinone mit azolhaltigen Tricyclen |
| DE19905278A1 (de) | 1999-02-09 | 2000-08-10 | Bayer Ag | Oxazolidinone und ihre Verwendung als antibakterielle Mittel |
| GB2351081A (en) | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Pharmaceutically active imidazoline compounds and analogues thereof |
| JP2001048786A (ja) | 1999-08-05 | 2001-02-20 | Yamanouchi Pharmaceut Co Ltd | 三環式ヘテロアリール誘導体 |
| DE19948434A1 (de) | 1999-10-08 | 2001-06-07 | Gruenenthal Gmbh | Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine |
| JP2001192386A (ja) | 1999-10-29 | 2001-07-17 | Meiji Seika Kaisha Ltd | 新規トリアゾール誘導体及びこれを有効成分とする抗真菌剤 |
| DE10019714A1 (de) | 2000-04-20 | 2002-01-10 | Gruenenthal Gmbh | Salze von bicyclischen, N-acylierten Imidazo-3-aminen und Imidazo-5-aminen |
| CA2415815A1 (en) | 2000-07-06 | 2002-01-17 | Nigel H. Greig | Tetrahydrobenzothiazole analogues as neuroprotective agents |
| US6696441B1 (en) | 2000-08-11 | 2004-02-24 | The Regents Of The University Of California | Inhibition of p53-induced stress response |
| US7601846B2 (en) | 2001-06-26 | 2009-10-13 | The Regents Of The University Of California | Compounds having activity as inhibitors of apoptosis |
| WO2003031587A2 (en) | 2001-10-09 | 2003-04-17 | The Regents Of The University Of California | Use of stat-6 inhibitors as therapeutic agents |
| US20040127719A1 (en) | 2002-03-08 | 2004-07-01 | Kexin Yang | Alpha-isocyanocarboxylate solid support templates, method of preparation and for using the same |
| AR040661A1 (es) * | 2002-07-26 | 2005-04-13 | Theravance Inc | Diclorhidrato cristalino de n-{2-[-((r)-2-hidroxi-2-feniletilamino)fenil]etil}-(r)-2hidroxi-2-(3-formamido-4-hidroxifenil)etilamina, agonista del receptor adrenergico beta 2 |
| MXPA05005474A (es) | 2002-11-25 | 2005-07-25 | Pharmacia Corp | Acidos y amidas heteroarilsulfonilmetil hidroxamicos y su uso como inhibidores de proteasas. |
| WO2004058758A1 (en) | 2002-12-18 | 2004-07-15 | Mallinckrodt Inc. | Synthesis of heteroaryl acetamides |
| KR100647583B1 (ko) | 2003-10-07 | 2006-11-17 | 삼성에스디아이 주식회사 | 이미다졸 고리 함유 화합물 및 이를 이용한 유기 전계발광 소자 |
| WO2005048953A2 (en) | 2003-11-13 | 2005-06-02 | Ambit Biosciences Corporation | Amide derivatives as kinase modulators |
| KR101449057B1 (ko) * | 2006-03-17 | 2014-10-10 | 암비트 바이오사이언시즈 코포레이션 | 질환 치료용 이미다졸로티아졸 화합물 |
| BRPI0816904B8 (pt) | 2007-09-19 | 2021-12-07 | Ambit Biosciences Corp | Forma cristalna b da forma sólida do sal de bis-hcl, composição farmacêutica, e, uso de uma forma sólida |
| AU2008325141B2 (en) | 2007-11-08 | 2014-03-20 | Ambit Biosciences Corp. | Methods of administering N-(5-tert-butyl-isoxazol-3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea to treat proliferative disease |
-
2008
- 2008-09-19 BR BRPI0816904A patent/BRPI0816904B8/pt active IP Right Grant
- 2008-09-19 HU HUE08832577A patent/HUE027982T2/en unknown
- 2008-09-19 HR HRP20160520TT patent/HRP20160520T1/hr unknown
- 2008-09-19 DK DK08832577.4T patent/DK2201018T3/en active
- 2008-09-19 AR ARP080104110A patent/AR068528A1/es unknown
- 2008-09-19 EP EP08832577.4A patent/EP2201018B1/en active Active
- 2008-09-19 US US12/233,906 patent/US8883783B2/en active Active
- 2008-09-19 CN CN2008801167866A patent/CN101868465B/zh active Active
- 2008-09-19 AU AU2008302744A patent/AU2008302744B2/en active Active
- 2008-09-19 CA CA2696776A patent/CA2696776C/en active Active
- 2008-09-19 MX MX2010002295A patent/MX2010002295A/es active IP Right Grant
- 2008-09-19 TW TW097136260A patent/TWI437988B/zh active
- 2008-09-19 SI SI200831613A patent/SI2201018T1/sl unknown
- 2008-09-19 KR KR1020157023723A patent/KR20150104231A/ko not_active Ceased
- 2008-09-19 JP JP2010525832A patent/JP5462168B2/ja active Active
- 2008-09-19 PL PL08832577.4T patent/PL2201018T3/pl unknown
- 2008-09-19 KR KR1020107008302A patent/KR101572701B1/ko active Active
- 2008-09-19 WO PCT/US2008/010884 patent/WO2009038757A2/en not_active Ceased
- 2008-09-19 ES ES08832577.4T patent/ES2573292T3/es active Active
-
2010
- 2010-02-11 IL IL203926A patent/IL203926A/en active IP Right Grant
-
2014
- 2014-10-07 US US14/508,967 patent/US9585892B2/en active Active
-
2016
- 2016-05-24 CY CY20161100450T patent/CY1117583T1/el unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019514863A5 (enExample) | ||
| JP2018193382A5 (enExample) | ||
| ES2905973T3 (es) | Proceso para la preparación de diclorhidrato de 5-cloro-N2-(2-isopropoxi-5-metil-4-piperidin-4-il-fenil)-N4-[2-(propano-2-sulfonil)-fenil]-pirimidin-2,4-diamina | |
| ES2841308T3 (es) | Compuesto de pirrolidina novedoso y aplicación como agonista del receptor de melanocortina | |
| JP2017522276A5 (enExample) | ||
| JP2010530897A5 (enExample) | ||
| JP2020535168A5 (enExample) | ||
| JP6787995B2 (ja) | 細胞毒性ベンゾジアゼピン誘導体の調製方法 | |
| HRP20160520T1 (hr) | ČVRSTI OBLICI KOJI SADRŽE N-(5-TERC-BUTIL-IZOKSAZOL-3-IL)-N'-{4-[7-(2-MORFOLIN-4-IL-ETOKSI)IMIDAZO[2,1-b]BENZOTIAZOL-2-IL]FENIL}UREJU, NJIHOVI SASTAVI I NJIHOVE UPORABE | |
| CN104768948A (zh) | 作为选择性parp-1抑制剂的4-甲酰氨基-异二氢吲哚酮衍生物 | |
| JP2019532919A5 (enExample) | ||
| JP7347852B2 (ja) | 重水素化大環状化合物の調製方法 | |
| CN109956906A (zh) | 一种噁拉戈利关键中间体的制备方法 | |
| JP2007532560A5 (enExample) | ||
| WO2011086541A1 (en) | Novel polymorph of nilotinib monohydrochloride monohydrate | |
| KR20180114227A (ko) | 피리디닐아미노피리미딘 유도체의 메실레이트 염의 결정질 형태, 그의 제조 방법, 및 그의 용도 | |
| CN117164580A (zh) | 一种kras g12c抑制剂的制备方法及其中间体 | |
| JP2016510767A5 (enExample) | ||
| ES2733813T3 (es) | Proceso para preparar una forma cristalina de lenalidomida | |
| JP2015531354A5 (enExample) | ||
| WO2020046753A1 (en) | Parp inhibitors for treating cancer and asthma | |
| CN105985317B (zh) | 一种色瑞替尼的制备方法及其中间体 | |
| CN104072477B (zh) | 伊马替尼的精制方法 | |
| CN105272921A (zh) | 一种制备Ceritinib的方法及其中间体化合物 | |
| CN102731408A (zh) | 一种阿齐沙坦中间体及其制备方法 |