AR062134A1 - Erlotinib cristalino - Google Patents
Erlotinib cristalinoInfo
- Publication number
- AR062134A1 AR062134A1 ARP070103344A ARP070103344A AR062134A1 AR 062134 A1 AR062134 A1 AR 062134A1 AR P070103344 A ARP070103344 A AR P070103344A AR P070103344 A ARP070103344 A AR P070103344A AR 062134 A1 AR062134 A1 AR 062134A1
- Authority
- AR
- Argentina
- Prior art keywords
- erlotinib
- crystalline
- crystalline erlotinib
- solvent
- cristalino
- Prior art date
Links
- 239000005551 L01XE03 - Erlotinib Substances 0.000 title abstract 7
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 title abstract 7
- 229960001433 erlotinib Drugs 0.000 title abstract 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- 150000004923 Erlotinib derivatives Chemical class 0.000 abstract 1
- 101500025419 Homo sapiens Epidermal growth factor Proteins 0.000 abstract 1
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 229940116978 human epidermal growth factor Drugs 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- GVUGOAYIVIDWIO-UFWWTJHBSA-N nepidermin Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C(C)C)C(C)C)C1=CC=C(O)C=C1 GVUGOAYIVIDWIO-UFWWTJHBSA-N 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Se refiere a erlotinib cristalino y en particular al hidrato de erlotinib cristalino. El erlotinib cristalino puede estar contenido en una preparacion farmacéutica. El erlotinib cristalino puede producirse mediante la precipitacion a partir de una solucion que comprende erlotinib disuelto en un solvente, donde dicho solvente se selecciona entre metanol, etanol, isopropanol, acetona, acetonitrilo, cloroformo, 1,4-dioxano, tolueno y mezclas de los mismos. El erlotinib cristalino puede usarse para producir sales de erlotinib. Inhibidor del factor de crecimiento epidérmico humano relacionado con la tirosina quinasa, EGFR-TK, util para el tratamiento de trastornos proliferativos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82071406P | 2006-07-28 | 2006-07-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR062134A1 true AR062134A1 (es) | 2008-10-15 |
Family
ID=38603403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070103344A AR062134A1 (es) | 2006-07-28 | 2007-07-27 | Erlotinib cristalino |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7928114B2 (es) |
| EP (1) | EP2054393A1 (es) |
| CN (1) | CN101547910A (es) |
| AR (1) | AR062134A1 (es) |
| CA (1) | CA2659307A1 (es) |
| WO (1) | WO2008012105A1 (es) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007140439A2 (en) * | 2006-05-31 | 2007-12-06 | Abbott Laboratories | Compounds as cannabinoid receptor ligands and uses thereof |
| US8841334B2 (en) * | 2006-05-31 | 2014-09-23 | Abbvie Inc. | Compounds as cannabinoid receptor ligands and uses thereof |
| JP2010522760A (ja) | 2007-03-28 | 2010-07-08 | アボット・ラボラトリーズ | カンナビノイド受容体リガンドとしての１，３−チアゾール−２（３ｈ）−イリデン化合物 |
| US7872033B2 (en) * | 2007-04-17 | 2011-01-18 | Abbott Laboratories | Compounds as cannabinoid receptor ligands |
| EP2160393A1 (en) * | 2007-05-18 | 2010-03-10 | Abbott Laboratories | Novel compounds as cannabinoid receptor ligands |
| WO2009002538A2 (en) * | 2007-06-25 | 2008-12-31 | Plus Chemicals S.A. | Amorphous erlotinib, processes for the preparation thereof, and processes to prepare additional forms of erlotinib |
| WO2009007984A2 (en) * | 2007-07-11 | 2009-01-15 | Hetero Drugs Limited | An improved process for erlotinib hydrochloride |
| EP2176241B1 (en) | 2007-08-17 | 2015-12-23 | Hetero Drugs Limited | A novel hydrated form of erlotinib free base and a process for preparation of erlotinib hydrochloride polymorph form a substantially free of polymorph form b |
| US9193713B2 (en) * | 2007-10-12 | 2015-11-24 | Abbvie Inc. | Compounds as cannabinoid receptor ligands |
| CA2716857A1 (en) | 2008-03-11 | 2009-09-17 | Teodozyi Kolasa | Novel compounds as cannabinoid receptor ligands |
| CA2730226A1 (en) * | 2008-07-07 | 2010-01-14 | Plus Chemicals Sa | Crystalline forms of erlotinib base and erlotinib hcl |
| US8846730B2 (en) * | 2008-09-08 | 2014-09-30 | Abbvie Inc. | Compounds as cannabinoid receptor ligands |
| ES2556752T3 (es) * | 2008-09-16 | 2016-01-20 | Abbvie Bahamas Ltd. | Ligandos de receptores cannabinoides |
| KR101132937B1 (ko) | 2008-10-01 | 2012-04-06 | 주식회사종근당 | Ｎ-(3-에티닐페닐)-6,7-비스(2-메톡시에톡시)-4-퀴나졸린아민 납실레이트 염 |
| PA8854001A1 (es) * | 2008-12-16 | 2010-07-27 | Abbott Lab | Compuestos novedosos como ligandos de receptores de canabinoides |
| WO2010109443A1 (en) | 2009-03-26 | 2010-09-30 | Ranbaxy Laboratories Limited | Process for the preparation of erlotinib or its pharmaceutically acceptable salts thereof |
| WO2011058525A2 (en) | 2009-11-12 | 2011-05-19 | Ranbaxy Laboratories Limited | Processes for the preparation of erlotinib hydrochloride form a and erlotinib hydrochloride form b |
| KR101208956B1 (ko) | 2010-07-15 | 2012-12-06 | 주식회사 셀트리온제약 | 엘로티닙 다이클로로아세트산염 및 이를 포함하는 항암제 조성물 |
| CN101914068A (zh) * | 2010-08-14 | 2010-12-15 | 浙江华海药业股份有限公司 | 一种厄洛替尼碱的新晶型及其制备方法 |
| CN103420922B (zh) * | 2012-05-18 | 2016-08-31 | 重庆华邦制药有限公司 | 一种工业化生产盐酸厄洛替尼b型晶的方法 |
| WO2014023027A1 (zh) * | 2012-08-10 | 2014-02-13 | 上海创诺医药集团有限公司 | 盐酸埃罗替尼多晶型物及其制备方法 |
| CN103570634B (zh) * | 2012-08-10 | 2018-01-26 | 上海创诺医药集团有限公司 | 盐酸埃罗替尼多晶型物及其制备方法 |
| NZ630289A (en) | 2012-09-04 | 2016-08-26 | Shilpa Medicare Ltd | Crystalline erlotinib hydrochloride process |
| WO2014118737A1 (en) | 2013-01-31 | 2014-08-07 | Ranbaxy Laboratories Limited | Erlotinib salts |
| CN103145628B (zh) * | 2013-03-18 | 2015-04-22 | 齐鲁制药有限公司 | 一种厄洛替尼一水合物晶型i的制备方法 |
| CN104119284A (zh) * | 2013-04-28 | 2014-10-29 | 广东东阳光药业有限公司 | 厄洛替尼新晶型及其制备方法 |
| CN103508962B (zh) * | 2013-07-03 | 2016-04-13 | 山东金城医药化工股份有限公司 | 盐酸厄洛替尼b晶型的制备方法 |
| CN104230825B (zh) * | 2014-09-03 | 2016-07-06 | 山东金城医药股份有限公司 | 厄洛替尼碱一水合物晶型FormⅠ的制备方法 |
| WO2018089269A1 (en) * | 2016-11-09 | 2018-05-17 | Renotarget Therapeutics Inc. | Novel class of quinolone heterocyclic aromatic molecules for cancer treatment |
| CN106749048B (zh) * | 2017-01-14 | 2020-03-20 | 山东裕欣药业有限公司 | 一种盐酸厄洛替尼晶型化合物及其制备方法 |
| EP3849964A4 (en) | 2018-09-14 | 2022-06-08 | Hanmi Pharmaceutical Co., Ltd. | CRYSTALLINE FORMS OF A QUINAZOLE COMPOUND AND ITS HYDROCHLORIDE SALTS |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE205483T1 (de) * | 1995-03-30 | 2001-09-15 | Pfizer | Chinazolinderivate |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| CN101219999A (zh) | 1998-04-29 | 2008-07-16 | Osi药物公司 | N-(乙炔苯基)-6,7-双(2-甲氧基乙氧基)-4-喹唑啉胺甲磺酸盐无水物和一水合物 |
| RS49836B (sr) | 1999-03-31 | 2008-08-07 | Pfizer Products Inc., | Postupci i intermedijeri za dobijanje anti-kancernih jedinjenja |
| UA74803C2 (uk) | 1999-11-11 | 2006-02-15 | Осі Фармасьютікалз, Інк. | Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування |
| US7148231B2 (en) | 2003-02-17 | 2006-12-12 | Hoffmann-La Roche Inc. | [6,7-Bis(2-methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)amine hydrochloride polymorph |
| WO2007060691A2 (en) * | 2005-11-23 | 2007-05-31 | Natco Pharma Limited | A novel process for the preparation of erlotinib |
-
2007
- 2007-07-25 WO PCT/EP2007/006705 patent/WO2008012105A1/en not_active Ceased
- 2007-07-25 EP EP07801462A patent/EP2054393A1/en not_active Withdrawn
- 2007-07-25 CA CA002659307A patent/CA2659307A1/en not_active Abandoned
- 2007-07-25 CN CNA2007800358363A patent/CN101547910A/zh active Pending
- 2007-07-27 AR ARP070103344A patent/AR062134A1/es unknown
- 2007-07-27 US US11/829,482 patent/US7928114B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2054393A1 (en) | 2009-05-06 |
| US20080058355A1 (en) | 2008-03-06 |
| US7928114B2 (en) | 2011-04-19 |
| CA2659307A1 (en) | 2008-01-31 |
| WO2008012105A1 (en) | 2008-01-31 |
| CN101547910A (zh) | 2009-09-30 |
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