[go: up one dir, main page]

LU90011I2 - Remifentanil facultativement sous la forme d'un sel d'addition d'acide pharmaceutiquement acceptable y compris le chlorhydrate de remifentanil - Google Patents

Remifentanil facultativement sous la forme d'un sel d'addition d'acide pharmaceutiquement acceptable y compris le chlorhydrate de remifentanil

Info

Publication number
LU90011I2
LU90011I2 LU90011C LU90011C LU90011I2 LU 90011 I2 LU90011 I2 LU 90011I2 LU 90011 C LU90011 C LU 90011C LU 90011 C LU90011 C LU 90011C LU 90011 I2 LU90011 I2 LU 90011I2
Authority
LU
Luxembourg
Prior art keywords
lower alkyl
group
alkoxy
remifentanil
member selected
Prior art date
Application number
LU90011C
Other languages
English (en)
Original Assignee
Glaxo Wellcome Inc
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 Glaxo Wellcome Inc filed Critical Glaxo Wellcome Inc
Publication of LU90011I2 publication Critical patent/LU90011I2/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
    • C07D211/10Heterocyclic 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 radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
    • C07D211/14Heterocyclic 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 radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
    • 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
    • C07D211/36Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
LU90011C 1989-02-15 1997-01-24 Remifentanil facultativement sous la forme d'un sel d'addition d'acide pharmaceutiquement acceptable y compris le chlorhydrate de remifentanil LU90011I2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US31131189A 1989-02-15 1989-02-15
US07/448,497 US5019583A (en) 1989-02-15 1989-12-11 N-phenyl-N-(4-piperidinyl)amides useful as analgesics

Publications (1)

Publication Number Publication Date
LU90011I2 true LU90011I2 (fr) 1997-03-11

Family

ID=26977841

Family Applications (1)

Application Number Title Priority Date Filing Date
LU90011C LU90011I2 (fr) 1989-02-15 1997-01-24 Remifentanil facultativement sous la forme d'un sel d'addition d'acide pharmaceutiquement acceptable y compris le chlorhydrate de remifentanil

Country Status (22)

Country Link
US (1) US5019583A (fr)
EP (1) EP0383579B1 (fr)
JP (1) JP2895145B2 (fr)
KR (1) KR0160979B1 (fr)
AT (1) ATE140451T1 (fr)
AU (1) AU636330B2 (fr)
CA (1) CA2010011C (fr)
CY (1) CY2002A (fr)
CZ (1) CZ402591A3 (fr)
DE (2) DE69027794T2 (fr)
DK (1) DK0383579T3 (fr)
ES (1) ES2088961T4 (fr)
GR (1) GR3020719T3 (fr)
HK (1) HK78297A (fr)
IE (1) IE77156B1 (fr)
LU (1) LU90011I2 (fr)
MX (1) MX9203024A (fr)
NL (1) NL960030I2 (fr)
NZ (1) NZ232542A (fr)
PT (1) PT93137B (fr)
SG (1) SG47967A1 (fr)
SK (1) SK402591A3 (fr)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5130321A (en) * 1990-12-18 1992-07-14 Glaxo Inc. Analgesic n-phenyl-n-(3-or 1-3-me-4-piperidinyl)amides
US5214148A (en) * 1990-12-18 1993-05-25 Glaxo Inc. Analgesic N-phenyl-N-(3-OR1 -3-ME-4-piperidinyl)amides
GB9316863D0 (en) * 1993-08-13 1993-09-29 Glaxo Group Ltd Chemical process
US5466700A (en) * 1993-08-30 1995-11-14 Glaxo Wellcome Inc. Anesthetic use of N-phenyl-N-(4-piperidinyl)amides
US5866591A (en) * 1996-09-11 1999-02-02 Glaxo Wellcome Inc. Stable formulations of remifentanil
ATE306472T1 (de) * 1997-12-24 2005-10-15 Ortho Mcneil Pharm Inc (4)-(aryl(piperidin-4-yl) aminobenzamidderivate die an delta-opioid rezeptor binden
US6858018B1 (en) * 1998-09-28 2005-02-22 Vyteris, Inc. Iontophoretic devices
US6436959B1 (en) 1998-12-23 2002-08-20 Ortho-Mcneil Pharmaceutical, Inc. 4-[aryl(piperidin-4-yl)]aminobenzamides
US7074935B2 (en) 1999-12-06 2006-07-11 Mallinckrodt Inc. Methods for the syntheses of alfentanil, sufentanil and remifentanil
WO2001068604A2 (fr) 2000-03-14 2001-09-20 Sepracor, Inc. Piperidines 3-substituees comprenant un groupement uree et procedes d'utilisation de ces dernieres
ES2302742T5 (es) * 2000-07-31 2011-10-10 Nycomed Danmark Aps Pulverizador nasal para suministrar una composición farmacéutica.
WO2002096351A2 (fr) 2001-04-03 2002-12-05 Aryx Therapeutics Opioides a action ultrabreve pour application transdermique
AU2002361709A1 (en) * 2001-12-17 2003-06-30 Aryx Therapeutics Analgesic delivery systems and methods of use
JPWO2005030722A1 (ja) * 2003-09-29 2006-12-07 日本ケミファ株式会社 N−置換−n−(4−ピペリジニル)アミド誘導体
MXPA06013917A (es) 2004-06-18 2007-03-07 Neurosearch As Nuevos derivados de piperidina sustituidos con alquilo y su uso como inhibidores de la recaptacion del neurotransmisor monoamino.
US20090030041A1 (en) * 2004-09-14 2009-01-29 Toshihiro Takahashi N-substituted N-(4-piperidinyl) Amide Derivative
EP1966140A1 (fr) * 2005-11-17 2008-09-10 Mallinckrodt, Inc. Procede de synthetisation du remifentanil
JP2009524659A (ja) * 2006-01-24 2009-07-02 マリンクロッド・インコーポレイテッド レミフェンタニルの合成方法
CN101379032A (zh) * 2006-02-03 2009-03-04 马林克罗特公司 瑞芬太尼盐酸盐的晶型
EP1867635A1 (fr) * 2006-06-15 2007-12-19 Kern Pharma, S.L. Procédé de préparation de remifentanil, ses produits intermédiaires, leur application et procédé pour leur préparation
GB0613693D0 (en) * 2006-07-10 2006-08-16 Cenes Ltd Benzodiazepine salts (3)
RU2470935C2 (ru) 2006-07-10 2012-12-27 ПАЙОН ЮКей ЛИМИТЕД Бензодиазепиновые соли кратковременного действия и их полиморфные формы
WO2008045192A2 (fr) * 2006-10-05 2008-04-17 Mallinckrodt Inc. Procédé alternatif pour la préparation du remifentanil
AU2007325889A1 (en) * 2006-11-29 2008-06-05 Mallinckrodt Inc. New process for remifentanil synthesis
MX2010010675A (es) 2008-03-31 2010-11-25 Gen Hospital Corp Analogos de etomidato con propiedades farmacocineticas y farmacodinamicas mejoradas.
WO2010000282A1 (fr) * 2008-07-03 2010-01-07 Cilag Ag Procédé de fabrication de sels de n-phényl-n-(4-pipéridinyl)amide
WO2010053944A1 (fr) * 2008-11-04 2010-05-14 Cambrex Charles City, Inc. Procédé amélioré de fabrication de dérivés de la pipéridine
BR112012000606A2 (pt) 2009-07-10 2016-11-22 Brigham & Womens Hospital análogos de etomidato que não inibem a síntese de esteróides adrenocorticais
EP2450039A1 (fr) 2010-11-08 2012-05-09 PAION UK Ltd. Régime de dosage permettant la sédation avec CNS 7056 (Remimazolam)
IN2014DN06132A (fr) 2012-01-13 2015-08-14 Gen Hospital Corp
KR20150065873A (ko) 2012-10-08 2015-06-15 오클랜드 유니서비시즈 리미티드 케타민 유도체
AR094963A1 (es) 2013-03-04 2015-09-09 Ono Pharmaceutical Co Reacción de oxidación excelente en el índice de conversión
CN103728403B (zh) * 2013-08-30 2015-10-07 宜昌人福药业有限责任公司 一种盐酸瑞芬太尼原料药中有关物质的检测方法
EP3199523B1 (fr) 2016-01-29 2018-08-15 Bioka s. r.o. Le nouveau procédé de production de n-phényl-n- (4-pipéridinyl) des dérivés d'amides tels que le rémifentanil et carfentanil
PL3643704T3 (pl) 2018-10-26 2021-06-14 Hameln Pharma Gmbh Nowe produkty pośrednie do wytwarzania chlorowodorku remifentanilu
GB202010168D0 (en) 2020-07-02 2020-08-19 Johnson Matthey Plc Process for preparing remifentanil hydrochloride
CN114262320A (zh) * 2021-12-28 2022-04-01 宜昌人福药业有限责任公司 一种利用连续流微通道反应器制备苯胺基哌啶类药物的合成方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL284196A (fr) * 1961-10-10
US3655675A (en) * 1968-09-09 1972-04-11 Sterling Drug Inc N-(n-heteryl)-acylanilides
US3998834A (en) * 1975-03-14 1976-12-21 Janssen Pharmaceutica N.V. N-(4-piperidinyl)-n-phenylamides and -carbamates
US4179569A (en) * 1975-03-14 1979-12-18 Janssen Pharmaceutica N.V. N-(4-piperidinyl)-N-phenylamides
US4167574A (en) * 1978-03-13 1979-09-11 Janssen Pharmaceutica, N.V. N-phenyl-N-(4-piperidinyl)amides
US4584303A (en) * 1984-04-09 1986-04-22 The Boc Group, Inc. N-aryl-N-(4-piperidinyl)amides and pharmaceutical compositions and method employing such compounds
US4801721A (en) * 1984-08-16 1989-01-31 Ryan James W Stereospecific synthesis of carboxyalkyl peptides
CA1317940C (fr) * 1987-09-25 1993-05-18 Georges H. P. Van Daele N-(1-alkyl-3-hydroxy-4-piperidinyl) benzamides a substituant

Also Published As

Publication number Publication date
GR3020719T3 (en) 1996-11-30
US5019583A (en) 1991-05-28
EP0383579B1 (fr) 1996-07-17
CA2010011A1 (fr) 1990-08-15
ATE140451T1 (de) 1996-08-15
ES2088961T4 (es) 1996-12-01
CZ402591A3 (en) 1993-04-14
IE77156B1 (en) 1997-12-03
AU4973190A (en) 1990-08-23
SK402591A3 (en) 2000-09-12
NL960030I2 (nl) 1997-05-01
DE19675028I2 (de) 2002-11-07
ES2088961T3 (es) 1996-10-01
KR0160979B1 (ko) 1998-12-01
HK78297A (en) 1997-06-20
CA2010011C (fr) 1997-12-02
AU636330B2 (en) 1993-04-29
MX9203024A (es) 1992-07-01
KR900012906A (ko) 1990-09-03
CY2002A (en) 1997-12-05
DE69027794T2 (de) 1997-01-02
DK0383579T3 (da) 1996-10-14
EP0383579A1 (fr) 1990-08-22
SG47967A1 (en) 1998-04-17
IE900532L (en) 1990-08-15
PT93137A (pt) 1990-08-31
JPH02300167A (ja) 1990-12-12
NL960030I1 (nl) 1997-02-03
NZ232542A (en) 1992-06-25
DE69027794D1 (de) 1996-08-22
JP2895145B2 (ja) 1999-05-24
PT93137B (pt) 1996-02-29

Similar Documents

Publication Publication Date Title
LU90011I2 (fr) Remifentanil facultativement sous la forme d'un sel d'addition d'acide pharmaceutiquement acceptable y compris le chlorhydrate de remifentanil
LU90160I2 (fr) Naratriptan facultativement sous la forme d'un sel pharmaceutiquement acceptable ou d'un solvate y compris le chlorhydrate de naratriptan
SE0104334D0 (sv) Therapeutic agents
ATE33835T1 (de) Verbindung mit antibronchopneumopathischer wirkung, verfahren zur herstellung und sie enthaltende pharmazeutische zusammensetzungen.
MX11031A (es) Proceso para la preparacion de nuevas 1-fenil-3-naftaleniloxipropanaminas producto obtenido y composicion farmaceutica que lo incluye.
KR960037675A (ko) 벤조니트릴 및 벤조플루오라이드
EP0353955A3 (fr) Composés chimiques
MA27197A1 (fr) Sels de tolterodine
FI860878A0 (fi) Aminosyraderivat och foerfarande foer deras framstaellning.
CA2406266A1 (fr) Derive de pyridine-1-oxyde, et processus de transformation de ce derive en composes pharmaceutiquement efficace
DK26289A (da) Anvendelse af 1,4-disubstitueret piperidinyl til fremstilling af et farmaceutisk praeparat til behandling af insomnia
PT90725A (pt) Processo para a preparacao de novos compostos cefem
FI933719A0 (fi) 4-((2-bensotiazolyl)metylamino)-a-((3,4-difluorfenoxi)metyl)-1-piperidinetanol
ES2114722T3 (es) Procedimiento para preparar intermedios derivados del acido benzoico y agentes farmaceuticos benzotiofenos.
KR20210121989A (ko) 베타코로나바이러스 감염을 예방하기 위한 조성물
MA27492A1 (fr) Nouveaux derives antagonistes du recepteur de la vitronectine, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant
SE9900190D0 (sv) New compounds
DE69001004D1 (de) Zusammensetzung gegen leberkrankheiten.
JPS5585550A (en) 4-homoisotwistane amino acid amide
TH20641A (th) 6-[ไทรแอโซลิล[3-(ไทรฟลูออโรเมธิล)เฟนิล]เมธิล]-2-ควิโนลิโนนและ-ควิโนลีนไธโอน
SE9904416D0 (sv) Crystalline form
DK0420464T3 (da) 3-isoxazolonderivater, deres fremstilling af deres terapeutiske anvendelser