WO2014020467A3 - Process for the preparation of pyrazole substituted aminoheteroaryl compounds - Google Patents
Process for the preparation of pyrazole substituted aminoheteroaryl compounds Download PDFInfo
- Publication number
- WO2014020467A3 WO2014020467A3 PCT/IB2013/055699 IB2013055699W WO2014020467A3 WO 2014020467 A3 WO2014020467 A3 WO 2014020467A3 IB 2013055699 W IB2013055699 W IB 2013055699W WO 2014020467 A3 WO2014020467 A3 WO 2014020467A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- preparation
- present
- pyrazole substituted
- aminoheteroaryl compounds
- substituted aminoheteroaryl
- Prior art date
Links
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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention relates to an improved process for the preparation of pyrazole substituted aminoheteroaryl compounds. More particularly, the present invention provides highly pure 3-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-ylpyrazol-4- yl)pyridin-2-amine, its intermediates and preparation thereof. The process of the present invention is simple, convenient, does not use expensive chemicals and avoids use of tedious purification techniques. Invention also provides process intermediates, useful not only in the synthesis, but also useful for providing desired compound with high purity.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2354DE2012 | 2012-07-30 | ||
IN2354/DEL/2012 | 2012-07-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2014020467A2 WO2014020467A2 (en) | 2014-02-06 |
WO2014020467A3 true WO2014020467A3 (en) | 2014-03-27 |
Family
ID=48949195
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2013/055699 WO2014020467A2 (en) | 2012-07-30 | 2013-07-11 | Process for the preparation of pyrazole substituted aminoheteroaryl compounds |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2014020467A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106279112A (en) * | 2015-06-12 | 2017-01-04 | 浙江九洲药业股份有限公司 | A kind of Crizotinib intermediate and its preparation method and application |
US10377940B2 (en) | 2016-09-20 | 2019-08-13 | Saudi Arabian Oil Company | Cement having cross-linked polymers |
CN106632263B (en) * | 2016-12-19 | 2019-02-22 | 河南应用技术职业学院 | A kind of synthetic method of (R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010048131A1 (en) * | 2008-10-21 | 2010-04-29 | Vertex Pharmaceuticals Incorporated | C-met protein kinase inhibitors |
WO2011042389A2 (en) * | 2009-10-09 | 2011-04-14 | Bayer Cropscience Ag | Phenylpyri(mi)dinylazoles |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ552946A (en) | 2004-08-26 | 2010-09-30 | Pfizer | Pyrazole-substituted aminoheteroaryl compounds as protein kinase inhibitors |
CN101023064B (en) | 2004-08-26 | 2011-02-16 | 辉瑞大药厂 | Enantiomerically pure aminoheteroaryl compounds as protein kinase inhibitors |
CA2632286C (en) | 2005-12-05 | 2011-11-15 | Pfizer Products Inc. | Use of (r)-3-[1-(2,6-dichloro-3-fluror-phenyl)-ethoxyl]-5-(1-piperidin-4-yl-1h-pyrazol-4-yl)-pyridin-2-ylamine for treatment of cancer |
-
2013
- 2013-07-11 WO PCT/IB2013/055699 patent/WO2014020467A2/en active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010048131A1 (en) * | 2008-10-21 | 2010-04-29 | Vertex Pharmaceuticals Incorporated | C-met protein kinase inhibitors |
WO2011042389A2 (en) * | 2009-10-09 | 2011-04-14 | Bayer Cropscience Ag | Phenylpyri(mi)dinylazoles |
Non-Patent Citations (1)
Title |
---|
PIETER D. DE KONING ET AL: "Fit-for-Purpose Development of the Enabling Route to Crizotinib (PF-02341066)", ORGANIC PROCESS RESEARCH & DEVELOPMENT, vol. 15, no. 5, 16 September 2011 (2011-09-16), pages 1018 - 1026, XP055078841, ISSN: 1083-6160, DOI: 10.1021/op200131n * |
Also Published As
Publication number | Publication date |
---|---|
WO2014020467A2 (en) | 2014-02-06 |
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