MX2011011177A - Proceso para la preparacion de 4-(3-cloro-2-fluoro-anilino)-7-meto xi-6-[1-(n-metilcarbamoilmetil) piperidin-4-il] quinazolina. - Google Patents
Proceso para la preparacion de 4-(3-cloro-2-fluoro-anilino)-7-meto xi-6-[1-(n-metilcarbamoilmetil) piperidin-4-il] quinazolina.Info
- Publication number
- MX2011011177A MX2011011177A MX2011011177A MX2011011177A MX2011011177A MX 2011011177 A MX2011011177 A MX 2011011177A MX 2011011177 A MX2011011177 A MX 2011011177A MX 2011011177 A MX2011011177 A MX 2011011177A MX 2011011177 A MX2011011177 A MX 2011011177A
- Authority
- MX
- Mexico
- Prior art keywords
- methylcarbamoylmethyl
- quinazoline
- piperidin
- chloro
- preparation
- Prior art date
Links
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 title 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- DFJSJLGUIXFDJP-UHFFFAOYSA-N sapitinib Chemical compound C1CN(CC(=O)NC)CCC1OC(C(=CC1=NC=N2)OC)=CC1=C2NC1=CC=CC(Cl)=C1F DFJSJLGUIXFDJP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/12—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to hydrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Se describen procesos para preparar 4-(3-cloro-2- fluoroanilino)7-metoxL6-{[1-(N-metilcarbamoilmetil)piperidin-4- il]oxi}quinazolina, sus sales de lo mismo y los intermedios utilizados en el proceso.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17199409P | 2009-04-23 | 2009-04-23 | |
PCT/GB2010/050653 WO2010122340A2 (en) | 2009-04-23 | 2010-04-22 | Process 738 |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2011011177A true MX2011011177A (es) | 2011-11-18 |
Family
ID=42224659
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2011011177A MX2011011177A (es) | 2009-04-23 | 2010-04-22 | Proceso para la preparacion de 4-(3-cloro-2-fluoro-anilino)-7-meto xi-6-[1-(n-metilcarbamoilmetil) piperidin-4-il] quinazolina. |
Country Status (14)
Country | Link |
---|---|
US (1) | US8450482B2 (es) |
EP (1) | EP2421827A2 (es) |
JP (1) | JP2012524769A (es) |
KR (1) | KR20120007059A (es) |
CN (1) | CN102459174A (es) |
AR (1) | AR076407A1 (es) |
AU (1) | AU2010240717A1 (es) |
BR (1) | BRPI1013854A2 (es) |
CA (1) | CA2758610A1 (es) |
IL (1) | IL215388A0 (es) |
MX (1) | MX2011011177A (es) |
SG (1) | SG174893A1 (es) |
TW (1) | TW201041871A (es) |
WO (1) | WO2010122340A2 (es) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101272613B1 (ko) * | 2011-10-05 | 2013-06-10 | 한미사이언스 주식회사 | 1-(4-(4-(3,4-디클로로-2-플루오로페닐아미노)-7-메톡시퀴나졸린-6-일옥시)피페리딘-1-일)프로프-2-엔-1-온 염산염의 제조 방법 및 이에 사용되는 중간체 |
CN108503596A (zh) * | 2018-03-14 | 2018-09-07 | 盐城师范学院 | 一种新的厄洛替尼及其中间体的制备方法 |
CN108440420A (zh) * | 2018-03-22 | 2018-08-24 | 盐城师范学院 | 酪氨酸激酶抑制剂拉帕替尼及其关键中间体的制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200813014A (en) | 2002-03-28 | 2008-03-16 | Astrazeneca Ab | Quinazoline derivatives |
US6924285B2 (en) | 2002-03-30 | 2005-08-02 | Boehringer Ingelheim Pharma Gmbh & Co. | Bicyclic heterocyclic compounds, pharmaceutical compositions containing these compounds, their use and process for preparing them |
GB0320793D0 (en) * | 2003-09-05 | 2003-10-08 | Astrazeneca Ab | Chemical process |
MXPA06003113A (es) * | 2003-09-19 | 2006-06-20 | Astrazeneca Ab | Derivados de quinazolina. |
WO2005115145A2 (en) * | 2004-05-20 | 2005-12-08 | Wyeth | Quinone substituted quinazoline and quinoline kinase inhibitors |
WO2009138779A1 (en) * | 2008-05-13 | 2009-11-19 | Astrazeneca Ab | Combination comprising 4- (3-chloro-2-fluoroanilino) -7-meth0xy-6- { [1- (n-methylcarbamoylmethyl) piperidin- 4-yl] oxyjquinazoline |
EP2303276B1 (en) | 2008-05-13 | 2013-11-13 | AstraZeneca AB | Fumarate salt of 4-(3-chloro-2-fluoroanilino)-7-methoxy-6-{[1-(n-methylcarbamoylmethyl)piperidin-4-yl]oxy}quinazoline |
-
2010
- 2010-04-22 CN CN2010800288080A patent/CN102459174A/zh active Pending
- 2010-04-22 MX MX2011011177A patent/MX2011011177A/es not_active Application Discontinuation
- 2010-04-22 JP JP2012506579A patent/JP2012524769A/ja active Pending
- 2010-04-22 KR KR1020117027878A patent/KR20120007059A/ko not_active Withdrawn
- 2010-04-22 AU AU2010240717A patent/AU2010240717A1/en not_active Abandoned
- 2010-04-22 CA CA2758610A patent/CA2758610A1/en not_active Abandoned
- 2010-04-22 EP EP10715333A patent/EP2421827A2/en not_active Withdrawn
- 2010-04-22 SG SG2011068426A patent/SG174893A1/en unknown
- 2010-04-22 US US13/264,217 patent/US8450482B2/en not_active Expired - Fee Related
- 2010-04-22 WO PCT/GB2010/050653 patent/WO2010122340A2/en active Application Filing
- 2010-04-22 BR BRPI1013854A patent/BRPI1013854A2/pt not_active IP Right Cessation
- 2010-04-23 AR ARP100101374A patent/AR076407A1/es not_active Application Discontinuation
- 2010-04-23 TW TW099112893A patent/TW201041871A/zh unknown
-
2011
- 2011-09-26 IL IL215388A patent/IL215388A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2010122340A3 (en) | 2011-09-09 |
CN102459174A (zh) | 2012-05-16 |
JP2012524769A (ja) | 2012-10-18 |
TW201041871A (en) | 2010-12-01 |
AR076407A1 (es) | 2011-06-08 |
WO2010122340A8 (en) | 2011-12-15 |
IL215388A0 (en) | 2011-12-29 |
EP2421827A2 (en) | 2012-02-29 |
KR20120007059A (ko) | 2012-01-19 |
US8450482B2 (en) | 2013-05-28 |
US20120108814A1 (en) | 2012-05-03 |
CA2758610A1 (en) | 2010-10-28 |
AU2010240717A1 (en) | 2011-10-27 |
SG174893A1 (en) | 2011-11-28 |
BRPI1013854A2 (pt) | 2017-05-16 |
WO2010122340A2 (en) | 2010-10-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MY159522A (en) | Administration of dipeptidyl peptidase inhibitors | |
IL236922A0 (en) | Salts and solid forms of (4))-4)-3-(s-morpholinomethyl)benzyl)oxy)-1-oxoisoindoline-2-yl)piperidine-6,2-dione and compounds containing them and methods of their use | |
WO2012077136A3 (en) | Process for the preparation of benzimidazole derivatives and its salts | |
ATE535282T1 (de) | Benzoazepin-oxy-essigsäurederivate als ppar-delta-agonisten zur erhöhung von hdl-c, senkung von ldl-c sowie cholesterinsenkung | |
AU2011278832A8 (en) | Novel fused heterocyclic derivatives useful as c-Met tyrosine kinase inhibitors | |
MY161966A (en) | Methods and genotyping panels for detecting alleles, genomes, and transcriptomes | |
IL180859A0 (en) | Imatinib mesylate alpha form and production process therefor | |
EP2305995A4 (en) | Process for producing common rail, and common rail | |
MX2010008583A (es) | Novedosos formas cristalinas de acido 4-[4-(2-adamantilcarbamoil)- 5-ter-butil-pirazol-1-il]benzoico. | |
EA200900091A1 (ru) | Новые показания к применению прямых ингибиторов тромбина в лечении сердечно-сосудистых заболеваний | |
TN2010000299A1 (en) | Crystalline 2-(4-cyclopropanesulphonyl-phenyl)-n-pyrazin-2-yl-3-(tetrahydropy-ran-4-yl)-propionamide | |
ZA201103727B (en) | Sulfoximine-substituted anilinopyrimidine derivatives as cdk inhibitors, the production thereof, and use as medicine | |
MA33290B1 (fr) | Pipéridines substituées | |
MY183041A (en) | Fumarate salt of 4- (3-chloro-2-fluoroanilino) -7-methoxy-6- {[1- (n-methylcarbamoylmethyl) piperidin- 4-yl] oxy}quinazoline | |
MX2011011177A (es) | Proceso para la preparacion de 4-(3-cloro-2-fluoro-anilino)-7-meto xi-6-[1-(n-metilcarbamoilmetil) piperidin-4-il] quinazolina. | |
TW200745036A (en) | Chemical process | |
MA33291B1 (fr) | Pipéridines substituées | |
ZA201004467B (en) | Triazolopyridazines as pari inhibitors,production thereof,and use as medicaments | |
WO2010112589A3 (de) | Schnittschablone aus keramik | |
ZA200807281B (en) | CCR5 antagonists useful for treating HIV | |
HK1164285A (en) | Process for the preparation of 4-(3-chloro-2-fluoro-anilino)-7-methoxy-6-{[1-(n-methylcarbamoylmethyl)-piperidin- 4-yl]oxy}quinazoline | |
UA103998C2 (ru) | Дифумарат 4-(3-хлор-2-фторанилино)-7-метокси-6-{[1-(n-метилкарбамоилметил)пиперидин-4-ил]окси}хиназолина | |
WO2010061208A3 (en) | Combination comprising a quinazoline derivative and a taxane | |
EP2351928A4 (en) | Common rail, common rail holder, and method for producing common rail | |
IL217351A0 (en) | 2-amino-2-phenyl-alkanol derivatives, prepartion thereof, and pharmaceutical compositons containing same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |