IN2014KN01319A - - Google Patents
Info
- Publication number
- IN2014KN01319A IN2014KN01319A IN1319KON2014A IN2014KN01319A IN 2014KN01319 A IN2014KN01319 A IN 2014KN01319A IN 1319KON2014 A IN1319KON2014 A IN 1319KON2014A IN 2014KN01319 A IN2014KN01319 A IN 2014KN01319A
- Authority
- IN
- India
- Prior art keywords
- formula
- cinacalcet
- pharmaceutically acceptable
- acceptable salts
- ethylamine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
- C07C209/16—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
Abstract
A new efficient method of producing Cinacalcet of formula I and its pharmaceutically acceptable salts which consists in direct alkylation of (R) (1 naphthyl)ethylamine of formula III with 3 [3 (trifluoromethyl)phenyl]propanol of formula II in presence of a catalyst in an inert organic solvent. Use of Cinacalcet of formula I prepared by the claimed method in preparation of pharmaceutically acceptable salts of Cinacalcet.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CZ20110770A CZ2011770A3 (en) | 2011-11-25 | 2011-11-25 | Process for preparing cinacalcet |
PCT/CZ2012/000119 WO2013075679A1 (en) | 2011-11-25 | 2012-11-21 | A method of producing cinacalcet |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2014KN01319A true IN2014KN01319A (en) | 2015-10-16 |
Family
ID=47435672
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN1319KON2014 IN2014KN01319A (en) | 2011-11-25 | 2012-11-21 |
Country Status (7)
Country | Link |
---|---|
CN (1) | CN103958456B (en) |
BR (1) | BR112014012434A2 (en) |
CZ (1) | CZ2011770A3 (en) |
HU (1) | HUP1400341A3 (en) |
IL (1) | IL232678A (en) |
IN (1) | IN2014KN01319A (en) |
WO (1) | WO2013075679A1 (en) |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6011068A (en) | 1991-08-23 | 2000-01-04 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
US5504253A (en) | 1994-07-15 | 1996-04-02 | Nps Pharmaceuticals, Inc. | Amine preparation |
EP1275635A1 (en) | 1994-10-21 | 2003-01-15 | Nps Pharmaceuticals, Inc. | Calcium receptor-active compounds |
ES2332016T3 (en) * | 2005-05-16 | 2010-01-22 | Teva Pharmaceutical Industries Ltd. | PROCEDURE FOR THE PREPARATION OF CINACALCET HYDROCLORIDE. |
MX2007000983A (en) * | 2005-05-23 | 2007-04-16 | Teva Pharma | Processes for preparing cinacalcet hydrochloride crystal form i. |
US7393967B2 (en) | 2006-04-27 | 2008-07-01 | Teva Pharmaceutical Industries Ltd. | Process for the preparation of cinacalcet base |
WO2007127445A2 (en) | 2006-04-27 | 2007-11-08 | Teva Pharmaceutical Industries Ltd. | Process for the preparation of cinacalcet base |
US20100267988A1 (en) | 2006-06-08 | 2010-10-21 | Medichem, S.A. | Processes for preparing intermediate compounds useful for the preparation of cinacalcet |
ES2569483T3 (en) * | 2007-06-21 | 2016-05-11 | Amgen Inc. | Methods to synthesize cinacalcet and salts thereof |
WO2010049293A2 (en) * | 2008-10-28 | 2010-05-06 | Zach System S.P.A. | Process for preparing cinacalcet |
-
2011
- 2011-11-25 CZ CZ20110770A patent/CZ2011770A3/en not_active IP Right Cessation
-
2012
- 2012-11-21 WO PCT/CZ2012/000119 patent/WO2013075679A1/en active Application Filing
- 2012-11-21 IN IN1319KON2014 patent/IN2014KN01319A/en unknown
- 2012-11-21 BR BR112014012434A patent/BR112014012434A2/en not_active IP Right Cessation
- 2012-11-21 CN CN201280057515.4A patent/CN103958456B/en active Active
- 2012-11-21 HU HU1400341A patent/HUP1400341A3/en unknown
-
2014
- 2014-05-18 IL IL232678A patent/IL232678A/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CN103958456B (en) | 2015-10-21 |
HUP1400341A3 (en) | 2014-12-29 |
CN103958456A (en) | 2014-07-30 |
BR112014012434A2 (en) | 2017-06-06 |
CZ303627B6 (en) | 2013-01-16 |
HUP1400341A2 (en) | 2014-10-28 |
CZ2011770A3 (en) | 2013-01-16 |
IL232678A (en) | 2017-05-29 |
WO2013075679A1 (en) | 2013-05-30 |
IL232678A0 (en) | 2014-08-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR112014007674A2 (en) | method for producing 4,4-difluoro-3,4-dihydroisoquinoline derivatives | |
UY33317A (en) | NEW DERIVATIVES OF PIRAZOL | |
ECSP14000074A (en) | METHODS FOR PREPARING ANTIVIRAL NUCLEOTHICAL ANALOGUES | |
SG10201804021TA (en) | Methods of preparing inhibitors of influenza viruses replication | |
AR076027A1 (en) | METHODS AND INTERMEDIARIES FOR THE PREPARATION OF PHARMACEUTICAL AGENTS | |
MX2014002552A (en) | Pyrazole compound and use thereof for medical purposes. | |
BRPI1006534A2 (en) | salt of compound 1, process for preparing a salt of compound 1, and process for preparing a mixed salt of compound 1 | |
BR112014001769A2 (en) | Process for the preparation of 1,4-cyclohexanedimethanol | |
FR2975990B1 (en) | PROCESS FOR PREPARING A FLUORINE ORGANIC COMPOUND | |
ZA201305059B (en) | Organic amine salts of azilsartan,preparation method and use thereof | |
JO2930B1 (en) | New process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid | |
IN2014KN01319A (en) | ||
UA111329C2 (en) | Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid | |
ES2556470T3 (en) | Procedure for preparing [3 - [(6-chloro-3-pyridinyl) methyl] -2-thiazolidinyliden] cyanamide | |
JO3189B1 (en) | Novel method for SYNTHESISING (2E)-3-(3,4-DIMETHOXYPHENYL)PROP-2-ENENITRILE, AND USE FOR SYNTHESISING IVABRADINE AND THE ADDED SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID | |
JO3276B1 (en) | Method for synthesising 3,4-dimethoxybicyclo [4. 2. 0] octa-1,3,5-triene-7-carbonitrile and use for synthesising ivabradine and the added salts thereof with a pharmaceutically acceptable acid | |
MY159691A (en) | New process for the synthesis of 3-(2-bromo-4,5-dimethoxyphenyl)propanenitrile, and application in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid | |
BR112013015903A2 (en) | crystalline polymorph, process for preparing a polymorph, pharmaceutical composition, purified form of the polymorph, use of a polymorph, process for preparing a compound, and, compound. | |
MX2013002656A (en) | New process. | |
UA111156C2 (en) | METHOD OF SYNTHESIS OF IVABRADINE AND ITS ADDITIVE SALTS WITH PHARMACEUTICALLY ACCEPTABLE ACID | |
MX2013011705A (en) | New method for synthesising -(2-bromo-4,5-dimethoxyphenyl)propane nitrile, and application to the synthesis of ivabradine and the addition salts of same with a pharmaceutically acceptable acid. | |
WO2015092809A3 (en) | Fingolimod hydrochloride process | |
GEP20156369B (en) | New process for synthesis of ivabradine and addition salts therewith pharmaceutically acceptable acid | |
MX2014003770A (en) | Pures-(-)-9-fluoro-6,7-dihydro-8-(4-hydroxypiperidin-1-yl)-5-met hyl-1-oxo-1h,-5h-benzo[i,j]quinolizine-2- carboxylic acid l-arginine salt tetrahydrate and a process for its preparation. | |
RU2011124598A (en) | METHOD FOR PRODUCING 5-METOXY-4-AZATRICYCLO [4.3.1.13,8] UNDEC-4-ENA |