[go: up one dir, main page]

FI895564A0 - 2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistusmenetelmä - Google Patents

2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistusmenetelmä

Info

Publication number
FI895564A0
FI895564A0 FI895564A FI895564A FI895564A0 FI 895564 A0 FI895564 A0 FI 895564A0 FI 895564 A FI895564 A FI 895564A FI 895564 A FI895564 A FI 895564A FI 895564 A0 FI895564 A0 FI 895564A0
Authority
FI
Finland
Prior art keywords
phenylmethyl
dihydrochloride
piperazinyl
chlorophenyl
ethoxy
Prior art date
Application number
FI895564A
Other languages
English (en)
Swedish (sv)
Other versions
FI91862C (fi
FI91862B (fi
Inventor
Eric Cossement
Genevieve Motte
Guy Bodson
Jean Gobert
Original Assignee
Ucb Sa
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 Ucb Sa filed Critical Ucb Sa
Publication of FI895564A0 publication Critical patent/FI895564A0/fi
Application granted granted Critical
Publication of FI91862B publication Critical patent/FI91862B/fi
Publication of FI91862C publication Critical patent/FI91862C/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
FI895564A 1988-11-23 1989-11-22 2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistusmenetelmä FI91862C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888827391A GB8827391D0 (en) 1988-11-23 1988-11-23 Process for preparation of 2-(2-(4-((4-chlorophenyl)phenylmethyl)-1-pipera-zinyl)ethoxy)-acetic acid & its dihydrochloride
GB8827391 1988-11-23

Publications (3)

Publication Number Publication Date
FI895564A0 true FI895564A0 (fi) 1989-11-22
FI91862B FI91862B (fi) 1994-05-13
FI91862C FI91862C (fi) 1994-08-25

Family

ID=10647347

Family Applications (1)

Application Number Title Priority Date Filing Date
FI895564A FI91862C (fi) 1988-11-23 1989-11-22 2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistusmenetelmä

Country Status (16)

Country Link
KR (1) KR970009728B1 (fi)
AT (1) AT398971B (fi)
CA (1) CA1317300C (fi)
CY (1) CY1671A (fi)
DK (1) DK174543B1 (fi)
ES (1) ES2021907A6 (fi)
FI (1) FI91862C (fi)
GB (2) GB8827391D0 (fi)
GR (1) GR1000553B (fi)
HK (1) HK95892A (fi)
HU (1) HU205094B (fi)
NO (1) NO172342C (fi)
PH (1) PH25982A (fi)
PL (1) PL161379B1 (fi)
PT (1) PT92364B (fi)
SG (1) SG89492G (fi)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0885611A3 (en) * 1992-09-24 1999-01-07 Sepracor, Inc. Methods and compositions for treating allergic disorders using optically pure (+) cetirizine
AU703690B2 (en) * 1992-09-24 1999-04-01 Sepracor, Inc. Methods for treating allergic disorders using optically pure (+)cetirizine
ATE170749T1 (de) * 1992-09-24 1998-09-15 Sepracor Inc Verwendung von (-) cetirizin zur behandlung allergischer rhinitis und und asthma
GB9305282D0 (en) * 1993-03-15 1993-05-05 Ucb Sa Enantiomers of 1-(4-chlorophenyl)phenylmethyl)-4-(4-methylphenyl)sulphonyl)piperazine
US6469009B1 (en) 1996-04-08 2002-10-22 Ucb, S.A. Pharmaceutical compositions for the treatment of rhinitis
BE1010094A3 (fr) 1996-04-10 1997-12-02 Ucb Sa Nouveaux [2-(1-piperazinyl)ethoxy] methyle substitues.
BE1010095A3 (fr) * 1996-04-10 1997-12-02 Ucb Sa Procede de preparation de l'acide 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl] ethoxy]-acetique et de ses sels.
AU7455798A (en) 1997-06-04 1998-12-21 Nippon Shoji Kaisha, Ltd. Process for producing piperazinesulfonamide derivatives and salts thereof
EP0919550A1 (en) 1997-11-26 1999-06-02 Ucb, S.A. Pseudopolymorphic forms of 2-2-4-bis(4-fluorophenyl)methyl-1-piperazinyl-ethoxy acetic acid dihydrochloride
IL124195A (en) * 1998-04-23 2000-08-31 Chemagis Ltd Process for the preparation of esters of 2-¬4-¬4-chlorophenyl¾phenylmethyl¾-1-piperazinyl¬ethoxy¾acetic acid
GR990100135A (el) * 1999-04-22 2000-12-29 Genepharm �.�. Μεθοδος παρασκευης του 2-(2-[4-[4-χλωροφαινυλο)(φαινυλο)μεθυλο]πιπεραζινο]αιθοξυ) οξικου οξεος και του διυδροχλωρικου αλατος αυτου
JP2002249487A (ja) * 2001-02-22 2002-09-06 Sumitomo Chem Co Ltd 4−(tert−ブトキシカルボニル)ピペラジン誘導体、その光学活性な酸付加塩、それらの製造法、およびそれらを用いる光学活性な1−[(置換フェニル)フェニルメチル]ピペラジンの製造法。
US6977301B1 (en) 2001-05-29 2005-12-20 Ucb, S.A. Process for preparing (S) and (R)—2-[4-(4-chlorobenzhydryl)piperazin-1-yl]-ethoxyacetamide
US7199241B1 (en) 2001-05-29 2007-04-03 Ucb, S.A. Process for preparing (S) and (R)-2-[4-(4-chlorobenzhydryl)piperazin-1-yl]-ethoxyacetamide
PL378027A1 (pl) * 2003-01-23 2006-02-20 Ucb Farchim Sa Nowe pochodne piperazyny i ich zastosowanie jako związków pośrednich w syntezie
KR100503443B1 (ko) 2004-02-02 2005-07-22 한림제약(주) 광학적으로 활성인 세티리진 또는 그의 염의 제조방법
EP1858866B1 (en) * 2005-03-03 2009-06-10 Ucb Farchim, S.A. Pyroglutamate salts and their use in the optical resolution of intermediates for the synthesis of dextrocetirizine and levocetirizine
HU227325B1 (en) * 2005-12-08 2011-03-28 Egis Gyogyszergyar Nyrt Process for the production of an intermediate of (dextro- and levo)- cetirizine
WO2008110586A2 (en) 2007-03-12 2008-09-18 Krka, Tovarna Zdravil, D.D., Novo Mesto New process for the preparation of levocetirizine and intermediates thereof
SI22489A (sl) * 2007-03-12 2008-10-31 Krka, Tovarna Zdravil, D.D., Novo Mesto Nov postopek za pripravo levocetirizina in njegovih intermediatov
WO2008152650A1 (en) 2007-06-15 2008-12-18 Symed Labs Limited Process for preparation of substantially optically pure levorotatory and dextrorotatory enantiomers of cetirizine using novel intermediates
WO2009062036A2 (en) * 2007-11-09 2009-05-14 Dr. Reddy's Laboratories Ltd. Processes for preparing levocetirizine and pharmaceutically acceptable salts thereof
ATE499352T1 (de) 2007-11-21 2011-03-15 Synthon Bv Verfahren zur herstellung von n- (diphenylmethyl)piperazinen
US7989623B2 (en) 2007-11-21 2011-08-02 Synthon Bv Process for making n-(diphenylmethyl)piperazines
JP2011523659A (ja) 2008-06-02 2011-08-18 シプラ・リミテッド レボセチリジンの合成方法及びそれに使用する中間体
WO2009150147A1 (en) * 2008-06-11 2009-12-17 Krka, Tovarna Zdravil, D.D., Novo Mesto New process for the preparation of levocetirizine and intermediates thereof
KR100998067B1 (ko) 2008-09-08 2010-12-03 주식회사 삼오제약 비스(1-[(4-클로로페닐)페닐메틸]피페라진)-2,3-디벤조일 타르타르산 신규 중간체 염 및 이를 이용한 광학 활성적으로 순수한 1-[(4-클로로페닐)페닐메틸]피페라진을 분리하는 분리방법
US20110172425A1 (en) 2008-09-17 2011-07-14 Calyx Chemicals And Pharmaceuticals Pvt. Ltd. Novel water based process for the preparation of substituted diphenylmethyl piperazines
WO2010107404A1 (en) 2009-03-16 2010-09-23 Mahmut Bilgic Stable pharmaceutical combinations
TR201007652A2 (tr) 2010-09-20 2012-04-24 Bi̇lgi̇ç Mahmut Sinerjik etki.
TR201009398A2 (tr) 2010-11-11 2012-05-21 Bi̇lgi̇ç Mahmut Fiziksel özellikleri geliştirilmiş tablet formülasyonları
WO2012101475A1 (en) 2011-01-27 2012-08-02 Jubilant Life Sciences Limited An improved process for the preparation of antihistaminic drugs via a novel carbamate intermediate
CN103044355A (zh) * 2011-10-13 2013-04-17 湖南九典制药有限公司 合成左西替利嗪的关键中间体及其制备方法
KR101418404B1 (ko) 2012-01-06 2014-07-10 한미약품 주식회사 레보세티리진 또는 이의 약학적으로 허용가능한 염 및 몬테루카스트 또는 이의 약학적으로 허용가능한 염을 함유하는 안정한 경구투여용 약학 제제
KR102226833B1 (ko) 2013-06-28 2021-03-12 한미약품 주식회사 레보세티리진 및 몬테루카스트를 포함하는 안정성이 개선된 복합 과립 제형
CN104045607B (zh) * 2014-05-21 2016-04-13 丽珠医药集团股份有限公司 一种盐酸西替利嗪的纯化方法
CN105924409B (zh) * 2016-05-12 2019-01-08 浙江永宁药业股份有限公司 一种(r)-1-((2-氯苯基)-(苯基)-甲基)-哌嗪的拆分方法
CN111205247B (zh) * 2020-04-22 2020-08-14 湖南九典宏阳制药有限公司 左旋西替利嗪的制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI75816C (fi) * 1981-02-06 1988-08-08 Ucb Sa Foerfarande foer framstaellning av terapeutiskt aktiv 2-/4-(difenylmetyl)-1-piperazinyl/-aettiksyror eller dess amid.

Also Published As

Publication number Publication date
HU896131D0 (en) 1990-02-28
NO894651L (no) 1990-05-25
PT92364B (pt) 1995-07-18
NO172342C (no) 1993-07-07
GB2225321A (en) 1990-05-30
GR1000553B (el) 1992-08-26
FI91862C (fi) 1994-08-25
AT398971B (de) 1995-02-27
DK586789D0 (da) 1989-11-22
PL161379B1 (pl) 1993-06-30
CA1317300C (en) 1993-05-04
FI91862B (fi) 1994-05-13
HK95892A (en) 1992-12-11
SG89492G (en) 1992-12-04
GB8926243D0 (en) 1990-01-10
KR900007825A (ko) 1990-06-02
GR890100770A (en) 1990-12-31
DK586789A (da) 1990-05-24
NO894651D0 (no) 1989-11-22
PH25982A (en) 1992-01-13
CY1671A (en) 1993-05-14
ATA266589A (de) 1994-07-15
GB8827391D0 (en) 1988-12-29
DK174543B1 (da) 2003-05-19
HUT53627A (en) 1990-11-28
KR970009728B1 (ko) 1997-06-17
HU205094B (en) 1992-03-30
ES2021907A6 (es) 1991-11-16
NO172342B (no) 1993-03-29
PT92364A (pt) 1990-05-31
GB2225321B (en) 1992-04-08

Similar Documents

Publication Publication Date Title
FI895564A0 (fi) 2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistusmenetelmä
FI895563A0 (fi) Menetelmä 2-/2-/4-/(4-kloorifenyyli)fenyylimetyyli/-1-piperatsinyyli/etoksi/-etikkahapon ja sen dihydrokloridin valmistamiseksi
FI905444A0 (fi) Menetelmä terapeuttisesti käyttökelpoisten, aromaattisesti substituoitujen piperidiini- ja piperatsiinijohdannaisten valmistamiseksi
PH23202A (en) 2-(5-fluoronicotinoyl) acetic acid derivatives and process of preparation thereof
FI890931A7 (fi) Menetelmä 5-lipoksigenaasia inhiboivien 4-(4-fenyyli-1-piperatsinyyli)fenoleiden valmistamiseksi
FI892603A7 (fi) Menetelmä uusien, terapeuttisesti käyttökelpoisten 4-(kinolin-2-yylimetoksi)fenyylietikkahappojohdannaisten valmistamiseksi
FI903643A0 (fi) Menetelmä mikrohiukkasten muodossa olevan farmaseuttisen koostumuksen valmistamiseksi
FI942932A0 (fi) Farmaseuttinen koostumus ja menetelmä sen valmistamiseksi
FI921059A0 (fi) Menetelmä hyötyproteiinien erittämiseksi hiivoista
PT87243A (pt) Process for the preparation of aliphatic carboxamides and of pharmaceutical compounds containing them
FI893214A0 (fi) Polypeptidijohdannaisia ja menetelmä niiden valmistamiseksi
FI92065C (fi) Menetelmä farmaseuttisten piperidiinijohdannaisten valmistamiseksi
FI884110A7 (fi) Salbutamolia sisältävä laastari ja menetelmä sen valmistamiseksi
FI883005A0 (fi) Promotorer foer expression av fraemmande dna i metylotrofiska bakterier, deras tillvaratagande och deras anvaendning.
NO176099C (no) Analogifremgangsmåte for fremstilling av terapeutisk aktive 4-(2-okso-3-pyridyl)-kromanderivater
JPS57149282A (en) 2-(4-(diphenylmethyl)-1-piperazinyl)acetic acid and their derivatives as medicine
NO971583L (no) Fremgangsmåte for fremstilling av 2-£2-£4-£4-klorfenyl)fenylmetyl|-1-piperazinyl|etoksy|eddiksyre og dens salter
FI860123A0 (fi) Menetelmä 1- 2-/5-dimetyyliaminometyyli-2-(furyylimetyylitio)etyyli/ amino-1-metyyliamino-2-nitroeteenin ja sen hydrokloridin valmistamiseksi
PL287224A1 (en) Method of obtaining 2-(2-(4-(/4-chlorophenyl/phenylmethyl)-1-piperazinyl) ethoxy) acetic acid and its dihydrohloride
NO923550L (no) Vaksiner for aa forhindre furunkulose hos fisk
FR2623749B1 (fr) Chemise extensible pour l'archivage de documents et procede pour sa fabrication
FI824516A7 (fi) Uudet heterosykliset etikkahappojohdannaiset ja menetelmä niiden valmistamiseksi.
GB2131797B (en) New heterocyclic acetic acid derivatives and process for the preparation thereof
PT87245A (pt) A process for the manufacture of pharmaceutical preparations containing a steroid
NO923492L (no) Fremgangsmaate til behandling av en opploesning inneholdende eddiksyre i naervaer av halogen

Legal Events

Date Code Title Description
BB Publication of examined application
FG Patent granted

Owner name: UCB S.A.

MA Patent expired