WO2007135693A3 - Intermédiaires utiles pour la préparation d'un dérivé de la pipéridine antihistaminique - Google Patents

Intermédiaires utiles pour la préparation d'un dérivé de la pipéridine antihistaminique Download PDF

Info

Publication number
WO2007135693A3
WO2007135693A3 PCT/IN2007/000201 IN2007000201W WO2007135693A3 WO 2007135693 A3 WO2007135693 A3 WO 2007135693A3 IN 2007000201 W IN2007000201 W IN 2007000201W WO 2007135693 A3 WO2007135693 A3 WO 2007135693A3
Authority
WO
WIPO (PCT)
Prior art keywords
piperidine derivative
preparation
intermediates useful
antihistaminic piperidine
antihistaminic
Prior art date
Application number
PCT/IN2007/000201
Other languages
English (en)
Other versions
WO2007135693A2 (fr
Inventor
Chidambaram Venkate Srinivasan
Perminder Singh Johar
Lalit Wadhwa
Original Assignee
Ind Swift Lab Ltd
Chidambaram Venkate Srinivasan
Perminder Singh Johar
Lalit Wadhwa
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ind Swift Lab Ltd, Chidambaram Venkate Srinivasan, Perminder Singh Johar, Lalit Wadhwa filed Critical Ind Swift Lab Ltd
Publication of WO2007135693A2 publication Critical patent/WO2007135693A2/fr
Publication of WO2007135693A3 publication Critical patent/WO2007135693A3/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic 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
    • C07D211/08Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/73Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
    • C07C69/738Esters of keto-carboxylic acids or aldehydo-carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/74Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C69/757Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La présente invention concerne un procédé de préparation d'un dérivé de la pipéridine antihistaminique, notamment la fexofénadine et ses sels pharmaceutiquement acceptables, par l'utilisation de nouveaux intermédiaires synthétiques de formule (I) suivante, où R représente un alkyle inférieur ; R2 représente H, un cyclopropyle, R1 représente un alkyle, la 4-(hydroxy-diphényl-méthyl)-pipéridin-1-yle.
PCT/IN2007/000201 2006-05-18 2007-05-18 Intermédiaires utiles pour la préparation d'un dérivé de la pipéridine antihistaminique WO2007135693A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN1219/DEL/2006 2006-05-18
IN1219DE2006 2006-05-18

Publications (2)

Publication Number Publication Date
WO2007135693A2 WO2007135693A2 (fr) 2007-11-29
WO2007135693A3 true WO2007135693A3 (fr) 2009-06-11

Family

ID=38723705

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IN2007/000201 WO2007135693A2 (fr) 2006-05-18 2007-05-18 Intermédiaires utiles pour la préparation d'un dérivé de la pipéridine antihistaminique

Country Status (1)

Country Link
WO (1) WO2007135693A2 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE03757471T1 (de) 2002-06-10 2005-09-01 Teva Pharmaceutical Industries Ltd. Polymorphe form xvi von fexofenadin-hydrochlorid
CN102757382B (zh) * 2012-07-06 2013-11-27 启东东岳药业有限公司 非索非那定中间体的纯化方法
HUE047669T2 (hu) 2015-10-22 2020-05-28 Sanofi Aventis Deutschland Eljárás fexofenadin és az eljárásban használt köztitermékek elõállítására

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5750703A (en) * 1993-06-24 1998-05-12 Albany Molecular Research, Inc. Piperidine derivatives and process for their production
US6147217A (en) * 1997-02-04 2000-11-14 Sepracor Inc. Synthesis of terfenadine and derivatives
WO2002102776A1 (fr) * 2001-06-15 2002-12-27 Aventis Pharma Deutschland Gmbh Procede de production du derive fexofenadine de piperidine
WO2004054955A1 (fr) * 2002-12-16 2004-07-01 Ranbaxy Laboratories Limited Procede de preparation de la fexofenadine

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5750703A (en) * 1993-06-24 1998-05-12 Albany Molecular Research, Inc. Piperidine derivatives and process for their production
US6147217A (en) * 1997-02-04 2000-11-14 Sepracor Inc. Synthesis of terfenadine and derivatives
WO2002102776A1 (fr) * 2001-06-15 2002-12-27 Aventis Pharma Deutschland Gmbh Procede de production du derive fexofenadine de piperidine
WO2004054955A1 (fr) * 2002-12-16 2004-07-01 Ranbaxy Laboratories Limited Procede de preparation de la fexofenadine

Also Published As

Publication number Publication date
WO2007135693A2 (fr) 2007-11-29

Similar Documents

Publication Publication Date Title
EP1845081A4 (fr) Composé amide
MX367154B (es) Formas solidas de acido 3-(6-(1-(2,2-difluorobenzo[d] [1,3]dioxol-5-il)ciclopropancarboxamido)-3-metilpiridin-2-il)benz oico.
MY152281A (en) 4-pyrimidinesulfamide derivative
WO2008055013A3 (fr) 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms
WO2009095933A3 (fr) Procédé perfectionné et nouveau pour la préparation de bosentan
NZ592543A (en) 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds
NO20063597L (no) Acetylinske piperazinforbindelser og deres anvendelse som metabotrofiske glutamatreseptorantagonister
WO2009154754A3 (fr) Synthèse de dérivés de morpholine deutérés
WO2009127948A8 (fr) Composés aryl carboxamides à 5 éléments de 4-[3-(aryloxy)benzylidène]-3-méthyl pipéridine utiles comme inhibiteurs de la faah
IL204936A0 (en) Preparation of dihydropyrrol derivatives as intermediates
NO20071112L (no) Nye heterosykliske karboksylsyreamidderivater
NZ597638A (en) 5-fluoro-2-oxopyrimidine- 1(2h)-carboxylate derivatives
WO2009047499A3 (fr) Procédés de préparation de palipéridone et de ses sels pharmaceutiquement acceptables et d'intermédiaires pour une utilisation dans les procédés
EA201270421A1 (ru) 1,2-дигидро-2-оксохинолиновые соединения в качестве лигандов рецептора 5-нт
WO2009127949A8 (fr) Composés aryl carboxamides de 4-[3-(aryloxy)benzylidène]-3-méthyl pipéridine utiles comme inhibiteurs de la faah
WO2007135693A3 (fr) Intermédiaires utiles pour la préparation d'un dérivé de la pipéridine antihistaminique
MX2010009876A (es) Nuevo proceso para la preparacion de derivados de acido ciclohexanocarboxilico por medio del derivado de ciclohexanocarboxamida correspondiente.
WO2009075516A3 (fr) Procédé de préparation de pantoprazole sodique sesquihydrate
MX2010009926A (es) Nuevo proceso para la preparacion de derivados de acido ciclohexancarboxilico.
WO2007087164A3 (fr) Procédé de synthèse de rémifentanil
WO2009021943A3 (fr) Nouveau procédé de préparation
BG108435A (en) Novel crystalline forms of 4-[4-[4-(hydroxydiphenyl methyl)-1-piperidinyl]-1-hydroxybutyl]-alpha, alpha-dimethylbenzene acetic acid and its hydrochloride
TW200637856A (en) Process for producing thiazolidinedion compound and intermediate thereof
WO2010122580A3 (fr) Nouveaux composés inhibiteurs de rénine
NO20084691L (no) Piperidinerivater som er nyttige for bahandling av osteoarttitt og osteoartrose

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 07736608

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 07736608

Country of ref document: EP

Kind code of ref document: A2