FR14C0033I2 - Derives de phenyl-piperazine en tant qu'inhibiteurs du recaptage de la serotonine - Google Patents

Derives de phenyl-piperazine en tant qu'inhibiteurs du recaptage de la serotonine

Info

Publication number
FR14C0033I2
FR14C0033I2 FR14C0033C FR14C0033C FR14C0033I2 FR 14C0033 I2 FR14C0033 I2 FR 14C0033I2 FR 14C0033 C FR14C0033 C FR 14C0033C FR 14C0033 C FR14C0033 C FR 14C0033C FR 14C0033 I2 FR14C0033 I2 FR 14C0033I2
Authority
FR
France
Prior art keywords
phenyl
serotonin reuptake
reuptake inhibitors
piperazine derivatives
piperazine
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
FR14C0033C
Other languages
English (en)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
H Lundbeck AS
Original Assignee
H Lundbeck AS
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8160750&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR14C0033(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by H Lundbeck AS filed Critical H Lundbeck AS
Publication of FR14C0033I1 publication Critical patent/FR14C0033I1/fr
Application granted granted Critical
Publication of FR14C0033I2 publication Critical patent/FR14C0033I2/fr
Active legal-status Critical Current

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
    • C07D295/096Heterocyclic 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 separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • 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
    • C07D295/14Heterocyclic 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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/145Heterocyclic 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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • 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
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/70Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/08Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 not condensed with other rings
    • 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
    • C07D295/02Heterocyclic 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 containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027Heterocyclic 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 containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/033Heterocyclic 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 containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
FR14C0033C 2001-10-04 2014-04-16 Derives de phenyl-piperazine en tant qu'inhibiteurs du recaptage de la serotonine Active FR14C0033I2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA200101466 2001-10-04
PCT/DK2002/000659 WO2003029232A1 (fr) 2001-10-04 2002-10-02 Derives de phenyl-piperazine en tant qu'inhibiteurs du recaptage de la serotonine

Publications (2)

Publication Number Publication Date
FR14C0033I1 FR14C0033I1 (fr) 2014-06-13
FR14C0033I2 true FR14C0033I2 (fr) 2014-11-14

Family

ID=8160750

Family Applications (1)

Application Number Title Priority Date Filing Date
FR14C0033C Active FR14C0033I2 (fr) 2001-10-04 2014-04-16 Derives de phenyl-piperazine en tant qu'inhibiteurs du recaptage de la serotonine

Country Status (38)

Country Link
US (10) US7144884B2 (fr)
EP (2) EP1749818B1 (fr)
JP (3) JP3896116B2 (fr)
KR (3) KR100783346B1 (fr)
CN (1) CN1319958C (fr)
AR (2) AR036659A1 (fr)
AT (2) ATE386730T1 (fr)
AU (2) AU2002333220C1 (fr)
BE (1) BE2014C036I2 (fr)
BR (3) BR122012023120B8 (fr)
CA (1) CA2462110C (fr)
CO (1) CO5580746A2 (fr)
CY (3) CY1107924T1 (fr)
DE (2) DE60233608D1 (fr)
DK (2) DK1749818T3 (fr)
EA (2) EA011096B1 (fr)
EG (1) EG25095A (fr)
ES (2) ES2328725T3 (fr)
FR (1) FR14C0033I2 (fr)
HR (1) HRP20040220A2 (fr)
HU (3) HU228956B1 (fr)
IL (1) IL160655A0 (fr)
IS (2) IS2578B (fr)
LT (1) LTC1436271I2 (fr)
LU (1) LU92397I2 (fr)
ME (1) ME00039B (fr)
MX (1) MXPA04002959A (fr)
MY (1) MY140950A (fr)
NL (1) NL300652I2 (fr)
NO (3) NO326443B1 (fr)
NZ (1) NZ531556A (fr)
PL (2) PL210551B1 (fr)
PT (2) PT1749818E (fr)
RS (2) RS52865B (fr)
SI (1) SI1436271T1 (fr)
UA (2) UA81749C2 (fr)
WO (1) WO2003029232A1 (fr)
ZA (1) ZA200401583B (fr)

Families Citing this family (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA81749C2 (uk) 2001-10-04 2008-02-11 Х. Луннбек А/С Фенілпіперазинові похідні як інгібітори зворотного захоплення серотоніну
GB0305575D0 (en) * 2003-03-11 2003-04-16 Glaxo Group Ltd Novel compounds
HRP20080262T3 (hr) * 2003-04-04 2009-04-30 H. Lundbeck A/S Derivati 4-(2-feniloksifenil)-piperidin ili -1,2,3,6 tetrahidropiridin kao inhibitori ponovne apsorpcije serotonina
EA009417B1 (ru) * 2003-04-04 2007-12-28 Х. Лундбекк А/С Производные 4-(2-фенилоксифенил)пиперидина или -1,2,3,6-тетрагидропиридина в качестве ингибиторов обратного захвата серотонина
ZA200507181B (en) * 2003-04-04 2007-03-28 Lundbeck & Co As 4-(2-phenylsulfanyl-phenyl)-piperidine derivatives as serotonin reuptake inhibitors
UA81300C2 (en) * 2003-04-04 2007-12-25 Lundbeck & Co As H Derivates of 4-(2-fenilsulfanilfenil)-1,2,3,6-tetrahydropiridin as retarding agents of serotonin recapture
CA2521258C (fr) * 2003-04-04 2009-12-01 H. Lundbeck A/S Derives 4-(2-phenylsulfanyl-phenyl)-piperidines utilises en tant qu'inhibiteurs de reabsorption de la serotonine
ATE396970T1 (de) 2003-12-23 2008-06-15 Lundbeck & Co As H 2-(1h-indolylsulfanyl)-benzylaminderivate als ssri
AR052308A1 (es) * 2004-07-16 2007-03-14 Lundbeck & Co As H Derivados de 2-(1h-indolilsulfanil)-arilamina y una composicion farmaceutica que contiene al compuesto
WO2006084870A2 (fr) * 2005-02-10 2006-08-17 Neurosearch A/S Nouveaux derives d'homopiperazine substitues alkyle et leur utilisation en tant qu'inhibiteurs du recaptage des neurotransmetteurs de monoamine
US7629473B2 (en) 2005-06-17 2009-12-08 H. Lundbeck A/S 2-(1H-indolylsulfanyl)-aryl amine derivatives
AR054394A1 (es) * 2005-06-17 2007-06-20 Lundbeck & Co As H Derivados de 2- (1h-indolilsulfanil)-aril amina
AR054393A1 (es) * 2005-06-17 2007-06-20 Lundbeck & Co As H Derivados de benzo(b)furano y benzo(b)tiofeno, composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de neurotransmisores de amina biogenicos.
JP2007106746A (ja) * 2005-09-13 2007-04-26 Tosoh Corp 新規アリールホモピペラジン類、またはその塩と製造方法
KR101627901B1 (ko) 2006-06-16 2016-06-13 하. 룬트벡 아크티에 셀스카브 인지기능 장애의 치료를 위한, 세로토닌 재흡수, 5-ht3 및 5-ht1a 활성이 조합된 화합물로서의 1-[2-(2,4-디메틸페닐술파닐)-페닐]피페라진
DK2044020T3 (da) * 2006-06-16 2011-08-15 Lundbeck & Co As H Krystallinske former af 4-[2-(4-methylphenylsulfanyl)-phenyl]-piperidin med kombineret serotonin- og norepinephrin-genoptagelsesinhibering til behandling af neuropatisk smerte
JP7179035B2 (ja) * 2006-06-16 2022-11-28 ハー・ルンドベック・アクチエゼルスカベット 認識機能障害(cognitive impairment)を治療するための、組み合わされたセロトニン再取り込み、5-HT3および5-HT1A活性を有する化合物としての1-[2-(2,4-ジメチルフェニルスルファニル)-フェニル]ピペラジン
JP5318757B2 (ja) * 2006-06-16 2013-10-16 ハー・ルンドベック・アクチエゼルスカベット 神経因性疼痛の治療のための、組み合わされたセロトニンおよびノルエピネフリン再取り込み阻害を有する4−[2−(4−メチルフェニルスルファニル)−フェニル]ピペリジンの結晶形
UA95801C2 (ru) * 2006-06-16 2011-09-12 Х. Луннбек А/С Кристаллические формы 4-[2-(4-метилфенилсульфанил)-фенил]пиперидина с комбинированным ингибированием обратного захвата серотонина и норэпинефрина для лечения невропатической боли
TWI432194B (zh) * 2007-03-20 2014-04-01 Lundbeck & Co As H 4-〔2-(4-甲基苯硫基)苯基〕哌啶之新穎治療用途
TW200848411A (en) 2007-03-20 2008-12-16 Lundbeck & Co As H Novel therapeutic uses of 1-[2-(2, 4-dimethylphenylsulfanyl)phenyl]-piperazine
WO2008151632A1 (fr) 2007-06-15 2008-12-18 H.Lundbeck A/S 4-[2-(4-méthylphénylsulfanyl)phényl]pipéridine pour le traitement du syndrome du côlon irritable (ibs)
TWI405588B (zh) 2007-03-20 2013-08-21 Lundbeck & Co As H 4-〔2-(4-甲苯基硫基)-苯基〕哌啶之鹽類的液體調配物
TW200932233A (en) 2007-11-13 2009-08-01 Lundbeck & Co As H Therapeutic uses of compounds having combined SERT, 5-HT3 and 5-HT1a activity
AU2014200364B2 (en) * 2007-11-13 2015-09-17 H. Lundbeck A/S Therapeutic uses of compounds having combined SERT, 5-HT3 and 5-HT1A activity
TW200932225A (en) * 2007-12-14 2009-08-01 Lundbeck & Co As H 4-[2,3-difluoro-6-(2-fluoro-4-methyl-phenylsulfanyl)-phenyl]-piperidine
TW200938194A (en) * 2007-12-14 2009-09-16 Lundbeck & Co As H Therapeutic uses of compounds having affinity to the serotonin transporter, serotonin receptors and noradrenalin transporter
WO2009081259A1 (fr) * 2007-12-21 2009-07-02 Pfizer Inc. Dérivés phénoxy-pyridylés
UA98698C2 (en) * 2008-03-03 2012-06-11 Х. Луннбек А/С Phenylsulfanylphenyl-piperidines and process for the preparation thereof
SI2358675T1 (sl) 2008-11-14 2013-01-31 Theravance, Inc. 4-(2-(2-fluorofenoksimetil)fenil)piperidinske spojine
TW201033181A (en) * 2009-02-17 2010-09-16 Lundbeck & Co As H Purification of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine
WO2010121621A1 (fr) * 2009-04-24 2010-10-28 H. Lundbeck A/S Formulations liquides de sels de 1-[2-(2,4-diméthylphénylsulfanyl)- phényl]pipérazine
GEP20135950B (en) 2009-08-24 2013-10-25 H Lundbeck As New compositions containing 1-[2-(2,4-dimethyl-phenylsulfa-nyl)-phenyl]piperazine
JP5781527B2 (ja) * 2009-10-30 2015-09-24 ヤンセン ファーマシューティカ エヌ.ベー. 4−置換−2−フェノキシ−フェニルアミンデルオピオイド受容体調節因子
WO2011085291A1 (fr) 2010-01-11 2011-07-14 Theravance, Inc. Composés de type 1-(2-phénoxyméthylphényl)pipérazine comme inhibiteurs du recaptage de la sérotonine et de la norépinéphrine
EP2550252B1 (fr) * 2010-03-22 2015-05-06 Theravance Biopharma R&D IP, LLC Composés de 1-(2-phénoxyméthylhétéroaryl)pipéridine et pipérazine
US8920840B2 (en) 2010-04-30 2014-12-30 Takeda Pharmaceutical Company Limited Enteric tablet
WO2011136376A1 (fr) * 2010-04-30 2011-11-03 武田薬品工業株式会社 Comprimé à délitage intestinal
EP2407467A1 (fr) 2010-07-14 2012-01-18 Sandoz Ag Composés cristallins de 1-[4-(2-azépan-1-yl-éthoxy)-benzyl]-2-(4-hydroxyphényl)-3-méthyl-1H-indol-5-ol et d'acide lactique
TW201212918A (en) * 2010-08-23 2012-04-01 Lundbeck & Co As H Therapeutic uses of 1-[2-(2,4-dimethyl-phenylsulfanyl)phenyl]piperazine
PL3135656T3 (pl) 2011-06-20 2019-07-31 H. Lundbeck A/S Deuterowane 1-piperazyno-3-fenyloindany do leczenia schizofrenii
KR102035877B1 (ko) 2011-11-14 2019-10-23 알파시그마 에스.피.에이. 우울증이 있는 대상체를 위한 치료 양생법 선택을 위한 검정법 및 치료 방법
DK2800746T3 (da) 2012-01-03 2019-05-20 H Lundbeck As Fremgangsmåde til fremstilling af 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin
CN104797566B (zh) 2012-09-19 2017-07-07 桑多斯股份公司 沃替西汀氢溴酸盐的新结晶形式
MX362886B (es) 2012-12-13 2019-02-22 H Lundbeck As Composición sinérgica que comprende vortioxetina y donepezilo para incrementar los niveles de acetilcolina en el cerebro, y el uso de la misma en el tratamiento de una disfunción cognitiva.
ME02671B (fr) * 2013-02-22 2017-06-20 H Lundbeck As Procédé de fabrication de vortioxétine
CN105283442B (zh) * 2013-04-04 2018-04-13 斯洛文尼亚莱柯制药股份有限公司 用于合成1‑(2‑((2,4‑二甲基苯基)硫代)苯基)哌嗪的方法
CN104109135B (zh) * 2013-04-22 2018-10-26 江苏豪森药业集团有限公司 1-[2-(2,4-二甲基苯基硫烷基)-苯基]哌嗪的制备方法
IN2013MU03121A (fr) 2013-09-30 2015-07-17 Cadila Healthcare Ltd
EP2878596A1 (fr) 2013-11-29 2015-06-03 LEK Pharmaceuticals d.d. Synthèse de vortioxetine via des intermédiaires de (2-(pipérazine-1-yl)phényl)lithium
CN104710345B (zh) * 2013-12-17 2017-09-05 江苏恩华药业股份有限公司 用于制备4‑(2‑(4‑甲基苯基硫基))苯基哌啶的化合物、其制备方法及应用
MX368870B (es) 2013-12-20 2019-10-21 H Lundbeck As Uso de un antagonista de receptores de opioides con actividad kappa y vortioxetina para el tratamiento de trastorno depresivo con características melancólicas.
EP2894154A1 (fr) 2014-01-14 2015-07-15 LEK Pharmaceuticals d.d. Synthèse de vortioxetine via des intermédiaires de (2-(piperazine-1-yl)phényl)aniline
CN103788019B (zh) * 2014-01-22 2015-10-07 苏州明锐医药科技有限公司 沃替西汀的制备方法
EA029060B1 (ru) 2014-01-31 2018-02-28 Эгиш Дьёдьсердьяр Зрт. Способ получения солей вортиоксетина
EP2930171A1 (fr) 2014-04-07 2015-10-14 LEK Pharmaceuticals d.d. Synthèse de vortioxetine via intermédiaire de (2,4-diméthylphényl) (2-iodophényl)sulfane
CN104059030B (zh) * 2014-05-30 2016-05-04 镇江圣安医药有限公司 [(苯硫烷基)-苯基]哌嗪的衍生物及其药物组合物和用途
FR3023320B1 (fr) * 2014-07-03 2017-03-10 Ifp Energies Now Systeme et procede de stockage et de recuperation d'energie par gaz comprime avec stockage de la chaleur au moyen d'un echangeur radial
CZ2014471A3 (cs) 2014-07-08 2016-01-20 Zentiva, K.S. Způsob přípravy vortioxetinu
US9687484B2 (en) 2014-07-18 2017-06-27 Dipharma Francis S.R.L. Crystalline forms of an antidepressant compound
CN104146953A (zh) * 2014-07-24 2014-11-19 李雪梅 一种氢溴酸沃替西汀注射液
CN104292183B (zh) * 2014-09-29 2016-01-06 杨献美 一种抗抑郁药物沃替西汀的制备方法
WO2016079751A2 (fr) 2014-11-17 2016-05-26 Megafine Pharma (P) Ltd. Procédé de préparation de vortioxétine et de polymorphes de cette substance
ES2634496T3 (es) 2014-11-21 2017-09-28 Dipharma Francis S.R.L. Proceso para la preparación de un antidepresivo y los intermedios del mismo
CN104447622B (zh) * 2014-11-28 2017-01-04 郑州大明药物科技有限公司 氢溴酸沃替西汀β晶型的制备方法
CN104586756A (zh) * 2015-01-05 2015-05-06 万特制药(海南)有限公司 一种含沃替西汀的口服溶液及其制备方法
CZ201531A3 (cs) 2015-01-21 2016-08-03 Zentiva, K.S. Polymerem stabilizované amorfní formy vortioxetinu
CN104610195B (zh) * 2015-01-30 2017-06-27 上虞京新药业有限公司 沃替西汀的天冬氨酸盐或其水合物及其制备方法和用途
WO2016125191A2 (fr) 2015-02-04 2016-08-11 Mylan Laboratories Limited Procédés de préparation de bromhydrate de vortioxétine
WO2016125190A2 (fr) 2015-02-04 2016-08-11 Mylan Laboratories Limited Nouvelles formes cristallines de vortioxétine, prémélanges, et procédés pour la préparation de ceux-ci
WO2016135636A1 (fr) 2015-02-25 2016-09-01 Lupin Limited Procédé de préparation de vortioxétine
EP3274330A1 (fr) 2015-03-26 2018-01-31 Cipla Limited Procédé de fabrication d'inhibiteurs de la recapture de la sérotonine
CN104829557B (zh) * 2015-04-23 2017-06-27 山东百诺医药股份有限公司 一种新化合物1‑[2‑(2,4‑二甲基苯基硫基)苯基]‑2‑氧哌嗪及其制备方法和在沃替西汀合成中的应用
JO3456B1 (ar) 2015-05-13 2020-07-05 H Lundbeck As فيروتيوكسيتين بيروجلوتامات
EP3799873A1 (fr) 2015-07-17 2021-04-07 Institut Pasteur Agent récepteur-stimulant 5-hydroxytryptamine1b destiné à être utilisé comme promoteur de l'autorenouvellement de cellules et/ou la différenciation par satellite
US20180237386A1 (en) * 2015-08-19 2018-08-23 Amneal Pharmaceuticals Company Gmbh Process For Preparation Of Vortioxetine Hydrobromide
EP3362058B1 (fr) * 2015-10-14 2021-09-01 Institut Pasteur Agent de stimulation du récepteur 5-hydroxytryptamine 1b pour le traitement de l'infarctus du myocarde
CN105348204B (zh) * 2015-11-18 2018-09-14 乳源瑶族自治县大众药品贸易有限公司 1-杂环基-2-(杂芳基硫基)苯衍生物及其使用方法和用途
CN105461635B (zh) * 2015-11-18 2018-06-08 乳源瑶族自治县大众药品贸易有限公司 苯基哌嗪衍生物及其使用方法和用途
US11013830B2 (en) * 2015-11-20 2021-05-25 Institut Pasteur 5-hydroxytryptamine 1B receptor-stimulating agent for enhancing in vivo engraftment potential
WO2017162536A1 (fr) 2016-03-21 2017-09-28 H. Lundbeck A/S Promédicaments de vortioxétine
BR112018003930A2 (pt) 2016-07-01 2018-09-25 H Lundbeck As regimes de dosagem de vortioxetina para início rápido de efeito antidepressivo
AU2017295038B2 (en) * 2016-07-15 2022-09-22 Centre Hospitalier Sainte Anne Paris 5-hydroxytryptamine 1B receptor-stimulating agent for skin and/or hair repair
US20210284615A1 (en) * 2016-07-22 2021-09-16 Qingeng Li Vortioxetine analogue and use and preparation thereof
WO2018042168A1 (fr) 2016-08-29 2018-03-08 King, Lawrence Composition pharmaceutique stable de bromhydrate de vortioxétine
CN106349132B (zh) * 2016-08-30 2018-02-02 重庆植恩药业有限公司 沃替西汀中间体杂质及其制备方法和用途
US10519121B2 (en) 2016-12-30 2019-12-31 Apicore Us Llc Process and novel polymorphic form of vortioxetine and its pharmaceutically acceptable salts
CN108409729B (zh) * 2017-02-09 2020-11-24 广东东阳光药业有限公司 苯基八氢-1H-吡啶并[1,2-a]吡嗪衍生物及其用途
CN108409728B (zh) * 2017-02-09 2020-11-24 广东东阳光药业有限公司 苯基八氢-1H-吡啶并[1,2-a]吡嗪衍生物及其用途
US10428033B2 (en) 2017-02-15 2019-10-01 Piramal Enterprises Limited Process for the preparation of vortioxetine and salts thereof
US11020390B2 (en) 2017-02-17 2021-06-01 Unichem Laboratories Ltd Bioequivalent pharmaceutical composition of vortioxetine hydrobromide
EP3585388A4 (fr) 2017-02-23 2020-08-12 Unichem Laboratories Ltd Procédé amélioré de préparation et de purification de bromhydrate de vortioxétine
DK3615518T3 (da) 2017-04-25 2022-02-07 H Lundbeck As Fremgangsmåde til fremstillingen af vortioxetin hbr alpha-form
EP3412661A1 (fr) 2017-06-08 2018-12-12 Enantia, S.L. Co-cristaux de bromhydrate vortioxetine et du résorcinol
KR102026337B1 (ko) 2017-07-07 2019-09-27 영진약품 주식회사 1-[2-(2,4-디메틸페닐설파닐)페닐]피페라진의 신규염 및 이의 제조방법
CN107915685A (zh) * 2017-12-11 2018-04-17 重庆植恩药业有限公司 一种氢溴酸沃替西汀中间体的制备方法
CN108017595A (zh) * 2017-12-20 2018-05-11 安徽源久源科技有限公司 一种1-[2-(2,5-二甲基苯硫基)苯基]哌嗪的制备方法
ES2976985T3 (es) 2018-06-20 2024-08-14 Vio Ag Pharmaceuticals S A Enfoque de activación C-H organo-pseudocatalítica de un recipiente para la preparación de vortioxetina y producto intermedio de vortioxetina
CN108863986B (zh) * 2018-08-06 2020-01-21 广东东阳光药业有限公司 二氟甲基取代的苯基哌嗪衍生物及其用途
CN108727393B (zh) * 2018-08-06 2019-10-29 广东东阳光药业有限公司 苯基二氮杂双环衍生物及其用途
EP3870292A4 (fr) 2018-10-26 2022-11-09 The Research Foundation for The State University of New York Combinaison d'un inhibiteur de réabsorption spécifique de la sérotonine et d'un agoniste partiel du récepteur de la sérotonine 1a pour réduire la dyskinésie induite par l-dopa
KR20220163997A (ko) 2020-04-03 2022-12-12 하. 룬드벡 아크티에셀스카브 정서적 둔마의 예방 또는 치료를 위한 1-[2-(2,4-디메틸페닐설파닐)-페닐]피페라진
WO2022052391A1 (fr) 2020-09-10 2022-03-17 苏州富德兆丰生化科技有限公司 Procédé de synthèse de vortioxétine
GB2622880A (en) 2022-09-30 2024-04-03 Alkaloid Ad Skopje Palatable orodispersible formulation of vortioxetine
WO2025132869A1 (fr) 2023-12-21 2025-06-26 H. Lundbeck A/S Procédé de préparation de compositions pharmaceutiques de vortioxétine présentant de faibles quantités d'impuretés de nitrosamine
CN120774863A (zh) * 2024-04-02 2025-10-14 王春刚 一种烷基二胺取代双芳杂环基硫醚类化合物及其制备和在制备治疗和/或预防肿瘤药物中的应用
EP4681702A1 (fr) 2024-07-16 2026-01-21 PharmaPath S.A. Solution orale comprenant hydrobromure de vortioxétine

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CS151751B1 (fr) 1971-04-13 1973-11-19
CS151753B1 (fr) 1971-04-13 1973-11-19
CS151755B1 (fr) 1971-04-13 1973-11-19
CS151752B1 (fr) 1971-04-13 1973-11-19
YU163075A (en) 1975-07-21 1982-05-31 Science Union & Cie Process for preparing new phenoxy derivatives
US4241071A (en) 1977-01-27 1980-12-23 American Hoechst Corporation Antidepressant (α-phenyl-2-tolyl)azacycloalkanes
US4198417A (en) 1979-01-10 1980-04-15 American Hoechst Corporation Phenoxyphenylpiperidines
US4198419A (en) 1979-01-10 1980-04-15 American Hoechst Corporation Phenylthiophenylpiperidines
ES2004809A6 (es) 1987-07-29 1989-02-01 Ferrer Int Procedimiento de obtencion de nuevas 1-(2-(fenilmetil)fenil)piperazinas
GB9126311D0 (en) 1991-12-11 1992-02-12 Wellcome Found Substituted diphenylsulfides
US6048876A (en) * 1995-01-23 2000-04-11 Suntory Limited Medicament for the alleviation or treatment of symptom derived from ischemic disease and compound useful therefor
CZ293595A3 (cs) 1995-11-09 1999-12-15 Farmak A. S. Deriváty N,N-dimethyl-2-(arylthio)benzylaminu, jejich soli, způsoby jejich přípravy a jejich použití v léčivých přípravcích
FR2757160B1 (fr) * 1996-12-13 1999-03-12 Sanofi Sa 1-phenylalkyl-1,2,3,6-tetrahydropyridines
US6297239B1 (en) 1997-10-08 2001-10-02 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
EP0958280B1 (fr) * 1997-10-31 2005-05-04 Daiichi Suntory Pharma Co., Ltd. Rylpiperidinopropanol et derives d'arylpiperazinopropanol et produits pharmaceutiques contenant lesdits composes
MXPA01009915A (es) 1999-04-02 2003-08-20 Icos Corp Inhibidores de lfa-1 que se unen a los icam y usos de los mismos.
BR0012984A (pt) 1999-08-04 2002-07-16 Millennium Pharm Inc Método para tratar um estado associado com o mc4-r em um mamìfero, composto de ligação ao mc4-r, e, composição farmacêutica
JP2003509294A (ja) * 1999-09-14 2003-03-11 ファーマコペイア インコーポレイテッド マルチチャネル分散ヘッドを含む物品
BR0016952A (pt) * 1999-12-30 2002-10-08 Lundbeck & Co As H Compostos derivados de fenil-piperazina substituìdos, composição farmacêutica, uso e método
EP1246819A1 (fr) 1999-12-30 2002-10-09 H. Lundbeck A/S Procede de preparation de derives de benzene substitue
US6813639B2 (en) 2000-01-26 2004-11-02 Viaclix, Inc. Method for establishing channel-based internet access network
DE10033548C2 (de) 2000-07-11 2002-05-16 Wolfgang Papenbrock Verfahren zur Vorschau von Internetseiten
EP1370558B1 (fr) * 2001-01-23 2005-08-24 Eli Lilly And Company Derives de piperazine et de piperidine en tant qu'agonistes du recepteur de la melanocortine
WO2002062766A2 (fr) 2001-02-07 2002-08-15 Millennium Pharmaceuticals, Inc. Composes de liaison au recepteur de la melanocortine-4 et procedes d'utilisation de tels composes
UA81749C2 (uk) 2001-10-04 2008-02-11 Х. Луннбек А/С Фенілпіперазинові похідні як інгібітори зворотного захоплення серотоніну
CN100457738C (zh) * 2001-12-20 2009-02-04 H·隆德贝克有限公司 芳氧基苯基和芳硫基苯基衍生物
TW200505902A (en) 2003-03-20 2005-02-16 Schering Corp Cannabinoid receptor ligands
CA2521258C (fr) * 2003-04-04 2009-12-01 H. Lundbeck A/S Derives 4-(2-phenylsulfanyl-phenyl)-piperidines utilises en tant qu'inhibiteurs de reabsorption de la serotonine
WO2005000309A2 (fr) 2003-06-27 2005-01-06 Ionix Pharmaceuticals Limited Composes chimiques
KR101627901B1 (ko) * 2006-06-16 2016-06-13 하. 룬트벡 아크티에 셀스카브 인지기능 장애의 치료를 위한, 세로토닌 재흡수, 5-ht3 및 5-ht1a 활성이 조합된 화합물로서의 1-[2-(2,4-디메틸페닐술파닐)-페닐]피페라진

Also Published As

Publication number Publication date
US20180127389A1 (en) 2018-05-10
DK1436271T6 (da) 2022-06-27
ES2298425T7 (es) 2022-06-27
HUP0402313A2 (hu) 2005-02-28
CO5580746A2 (es) 2005-11-30
NO2014011I1 (no) 2014-05-13
HUP0402313A3 (en) 2010-03-29
MEP6508A (xx) 2010-02-10
US8110567B2 (en) 2012-02-07
US20210276966A1 (en) 2021-09-09
HU228956B1 (en) 2013-07-29
JP3955613B2 (ja) 2007-08-08
CY2014022I1 (el) 2015-12-09
CA2462110A1 (fr) 2003-04-10
EP1436271A1 (fr) 2004-07-14
IS2732B (is) 2011-04-15
JP2005505585A (ja) 2005-02-24
DE60233608D1 (de) 2009-10-15
KR100770194B1 (ko) 2007-10-25
JP2007051149A (ja) 2007-03-01
KR20040047886A (ko) 2004-06-05
US9090575B2 (en) 2015-07-28
US8476279B2 (en) 2013-07-02
IS7164A (is) 2004-02-26
US10844029B2 (en) 2020-11-24
EG25095A (en) 2011-08-17
WO2003029232A1 (fr) 2003-04-10
NO20041628L (no) 2004-04-21
DE60225162D1 (de) 2008-04-03
AU2002333220A2 (en) 2003-04-14
KR100842702B1 (ko) 2008-07-01
DK1749818T3 (da) 2009-10-12
ME00039B (fr) 2010-06-10
NL300652I1 (fr) 2016-01-18
SI1436271T1 (sl) 2008-06-30
HRP20040220A2 (en) 2005-02-28
EP1436271B1 (fr) 2008-02-20
ATE386730T1 (de) 2008-03-15
RS27704A (sr) 2006-10-27
ES2298425T3 (es) 2008-05-16
CA2462110E (fr) 2003-04-10
US7683053B2 (en) 2010-03-23
AU2002333220B2 (en) 2008-02-07
BR122012009534B1 (pt) 2018-02-27
HU230189B1 (hu) 2015-09-28
AU2006215994B2 (en) 2008-11-13
US20070060574A1 (en) 2007-03-15
ZA200401583B (en) 2005-05-25
US7148238B2 (en) 2006-12-12
DE60225162T2 (de) 2009-02-12
RS20120158A2 (sr) 2012-10-31
EP1749818B1 (fr) 2009-09-02
EP1749818A3 (fr) 2008-04-02
BE2014C036I2 (fr) 2021-11-22
CN1561336A (zh) 2005-01-05
US7144884B2 (en) 2006-12-05
AU2006215994A1 (en) 2006-10-05
BR0212733B1 (pt) 2014-05-13
NO20083446L (no) 2004-04-21
EA200400498A1 (ru) 2004-08-26
MXPA04002959A (es) 2004-07-05
RS52865B (sr) 2013-12-31
US20060089368A1 (en) 2006-04-27
LU92397I2 (fr) 2014-05-12
CY2014022I2 (el) 2015-12-09
AU2002333220C1 (en) 2023-10-05
AR036659A1 (es) 2004-09-22
BR122012023120B8 (pt) 2022-01-18
ES2328725T3 (es) 2009-11-17
DK1436271T3 (da) 2008-06-09
IS2578B (is) 2010-02-15
KR20070103515A (ko) 2007-10-23
AU2006215994A2 (en) 2006-10-05
KR100783346B1 (ko) 2007-12-07
EP1436271B3 (fr) 2022-04-20
AR066460A2 (es) 2009-08-19
US20060084662A1 (en) 2006-04-20
US20110009423A1 (en) 2011-01-13
BR122012009534B8 (pt) 2019-01-29
NO326443B1 (no) 2008-12-08
CY1107924T1 (el) 2013-09-04
EA011096B1 (ru) 2008-12-30
EA200601269A1 (ru) 2007-02-27
PL368442A1 (pl) 2005-03-21
LTC1436271I2 (lt) 2016-09-12
US9708280B2 (en) 2017-07-18
US7138407B2 (en) 2006-11-21
IS8806A (is) 2009-03-10
CY1110064T1 (el) 2015-01-14
CA2462110C (fr) 2010-05-11
IL160655A0 (en) 2004-07-25
AU2006215994A9 (en) 2006-10-05
ATE441631T1 (de) 2009-09-15
NO2014011I2 (no) 2015-08-31
US20160137620A1 (en) 2016-05-19
JP2007031447A (ja) 2007-02-08
EA007537B3 (ru) 2015-02-27
BRPI0212733B8 (pt) 2021-05-25
EP1749818A2 (fr) 2007-02-07
NL300652I2 (fr) 2016-01-18
BR122012023120B1 (pt) 2017-03-21
CN1319958C (zh) 2007-06-06
HUS1400012I1 (hu) 2020-12-28
FR14C0033I1 (fr) 2014-06-13
PL210551B1 (pl) 2012-02-29
NO332355B1 (no) 2012-09-03
PT1749818E (pt) 2009-10-06
PL209253B1 (pl) 2011-08-31
UA81749C2 (uk) 2008-02-11
HK1072600A1 (zh) 2005-09-02
MY140950A (en) 2010-02-12
LTPA2014013I1 (lt) 2014-04-25
JP3955614B2 (ja) 2007-08-08
DE60225162T3 (de) 2022-08-11
EA007537B1 (ru) 2006-10-27
JP3896116B2 (ja) 2007-03-22
US20050014740A1 (en) 2005-01-20
UA93857C2 (uk) 2011-03-25
NZ531556A (en) 2005-12-23
RS52326B (sr) 2012-12-31
PT1436271E (pt) 2008-04-10
BR0212733A (pt) 2004-11-16
BR122012009534C8 (pt) 2021-05-25
RS20120158A3 (en) 2013-10-31
KR20060118020A (ko) 2006-11-17
US20140163043A1 (en) 2014-06-12
US20120302553A1 (en) 2012-11-29

Similar Documents

Publication Publication Date Title
CY2014022I2 (el) Παραγωγα φαινυλ-πιπεραζινης ως αναστολεις επαναπροσληψης σεροτονινης
FR20C1039I2 (fr) Derives de l'uk-2a
NO20034307D0 (no) Cyklopropylindol-derivater som selektive serotonin- gjenopptaksinhibitorer
FR15C0086I2 (fr) Derives d'hydroxamate en tant qu'inhibiteurs de desacetylase
FR18C1024I2 (fr) Derives d'heterocyclocarboxamide
FR15C0068I2 (fr) Derives de diamine
NO20043022L (no) 5,6-diaryl-pyrazin-2-amid-derivater som CB1-antagonister
EP1415974A4 (fr) Procede de production de derives fluores du norbornene
NO20030842L (no) Fenoksybenzylaminderivater som selektive serotonin- gjenopptaksinhibitorer
EP1577361A4 (fr) Composition de pulverisation
NO20021251D0 (no) Tienoisoksazolyl- og tienylpyrrazolyl-fenoksysubstituerte propylderivater anvendelige som D4antagonister
EE200300498A (et) Fenüül-heterotsüklüüleetri derivaadid kui serotoniini tagasihaarde inhibiitorid
DZ3489A1 (fr) Procede de preparation de mesylates de derives de piperazine
EP1450790A4 (fr) Derives de carbamate photosensibilisants
FR2833596B1 (fr) Procede de preparation de derives d'echinocandine
DK1406888T3 (da) Substituerede gamma-lactonforbindelser som NMDA-antagonister
EP1829864A4 (fr) Derives d'isoquiline utiles en tant qu'inhibiteurs de la calpaine
DE60323748D1 (de) 1,3-diaza-dibenzoazulene als inhibitoren der produfür deren herstellung
EP1192128A4 (fr) Derives de thiol servant d'inhibiteurs des metallo-beta-lactamases
ITMI20011718A0 (it) Processo per la preparazione del sale sodico dell'acido-6(d-(-)-alpha-(4-etil-2,3-diosso-1-piperazinocarbonilammino)fenilacetammido)penicill
NO20040913L (no) Nye 2,4-diaminotiazolderivater