PT93137A - Processo para a preparacao de n-fenil-n-(4-piperidinil) amidas - Google Patents

Processo para a preparacao de n-fenil-n-(4-piperidinil) amidas

Info

Publication number
PT93137A
PT93137A PT93137A PT9313790A PT93137A PT 93137 A PT93137 A PT 93137A PT 93137 A PT93137 A PT 93137A PT 9313790 A PT9313790 A PT 9313790A PT 93137 A PT93137 A PT 93137A
Authority
PT
Portugal
Prior art keywords
lower alkyl
group
alkoxy
member selected
carbonyl
Prior art date
Application number
PT93137A
Other languages
English (en)
Other versions
PT93137B (pt
Inventor
Paul L Feldman
Michael K James
Marcus F Brackeen
Michael Ross Johnson
Harry Jefferson Leighton
Original Assignee
Glaxo 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 Inc filed Critical Glaxo Inc
Publication of PT93137A publication Critical patent/PT93137A/pt
Publication of PT93137B publication Critical patent/PT93137B/pt

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)
  • Medicinal Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (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)
PT93137A 1989-02-15 1990-02-14 Processo para a preparacao de n-fenil-n-(4-piperidinil) amidas PT93137B (pt)

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 (2)

Publication Number Publication Date
PT93137A true PT93137A (pt) 1990-08-31
PT93137B PT93137B (pt) 1996-02-29

Family

ID=26977841

Family Applications (1)

Application Number Title Priority Date Filing Date
PT93137A PT93137B (pt) 1989-02-15 1990-02-14 Processo para a preparacao de n-fenil-n-(4-piperidinil) amidas

Country Status (22)

Country Link
US (1) US5019583A (pt)
EP (1) EP0383579B1 (pt)
JP (1) JP2895145B2 (pt)
KR (1) KR0160979B1 (pt)
AT (1) ATE140451T1 (pt)
AU (1) AU636330B2 (pt)
CA (1) CA2010011C (pt)
CY (1) CY2002A (pt)
CZ (1) CZ402591A3 (pt)
DE (2) DE19675028I2 (pt)
DK (1) DK0383579T3 (pt)
ES (1) ES2088961T4 (pt)
GR (1) GR3020719T3 (pt)
HK (1) HK78297A (pt)
IE (1) IE77156B1 (pt)
LU (1) LU90011I2 (pt)
MX (1) MX9203024A (pt)
NL (1) NL960030I2 (pt)
NZ (1) NZ232542A (pt)
PT (1) PT93137B (pt)
SG (1) SG47967A1 (pt)
SK (1) SK402591A3 (pt)

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
JP4754068B2 (ja) * 1997-12-24 2011-08-24 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド δ−オピオイドレセプターに結合する4−[アリール(ピペリジン−4−イル)]アミノベンズアミド類
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
AU2427201A (en) 1999-12-06 2001-06-12 Mallinckrodt, Inc. New methods for the syntheses of alfentanil, sufentanil and remifentanil
US6476050B2 (en) 2000-03-14 2002-11-05 Sepracor, Inc. 3-substituted piperidines comprising urea functionality, and methods of use thereof
DE20122843U1 (de) * 2000-07-31 2008-06-26 Nycomed Danmark Aps Fentanyl Zusammensetzung zur nasalen Anwendung
JP2005503351A (ja) 2001-04-03 2005-02-03 アリックス セラピューティクス 経皮適用のための超短時間作用性オピオイド
US20030130314A1 (en) * 2001-12-17 2003-07-10 Pascal Druzgala Analgesic delivery systems and methods of use
WO2005030722A1 (ja) * 2003-09-29 2005-04-07 Nippon Chemiphar Co., Ltd. N-置換-n-(4-ピペリジニル)アミド誘導体
JP2008502651A (ja) 2004-06-18 2008-01-31 ノイロサーチ アクティーゼルスカブ モノアミン神経伝達物質再取込み阻害剤としての、新規アルキル置換ピペリジン誘導体及びその使用
EP1795526A4 (en) * 2004-09-14 2010-10-13 Nippon Chemiphar Co N-SUBSTITUTED N- (4-PIPERIDINYL) AMIDE DERIVATIVE
EP1966140A1 (en) * 2005-11-17 2008-09-10 Mallinckrodt, Inc. Process for synthesizing remifentanil
US20080312448A1 (en) * 2006-01-24 2008-12-18 Cheng Brian K Process for Synthesizing Remifentanil
JP2009525329A (ja) * 2006-02-03 2009-07-09 マリンクロッド・インコーポレイテッド レミフェンタニル塩酸塩の結晶形
EP1867635A1 (en) * 2006-06-15 2007-12-19 Kern Pharma, S.L. Process for preparing remifentanil, intermediates thereof, use of said intermediates and processes for their preparation
KR20170091770A (ko) 2006-07-10 2017-08-09 파이온 유케이 리미티드 속효형 벤조디아제핀 염 및 이의 중합체 형태
GB0613693D0 (en) * 2006-07-10 2006-08-16 Cenes Ltd Benzodiazepine salts (3)
WO2008045192A2 (en) * 2006-10-05 2008-04-17 Mallinckrodt Inc. Alternate process for remifentanil preparation
CA2670704A1 (en) * 2006-11-29 2008-06-05 Mallinckrodt Inc. New process for remifentanil synthesis
JP5580287B2 (ja) * 2008-03-31 2014-08-27 ザ ジェネラル ホスピタル コーポレイション 改善された薬物速度論的および薬力学的特性を有するエトミデート類似体
US20110144346A1 (en) * 2008-07-03 2011-06-16 Cilag Ag Method for producing n-phenyl-n-(4-piperidinyl) amide salts
US8299258B2 (en) * 2008-11-04 2012-10-30 Cambrex Charles City Method of making piperidine derivatives
RU2559888C2 (ru) 2009-07-10 2015-08-20 Зе Дженерал Хоспитал Корпорэйшн Аналоги этомидата, которые не ингибируют синтез адренокортикостероидов
EP2450039A1 (en) 2010-11-08 2012-05-09 PAION UK Ltd. Dosing regimen for sedation with CNS 7056 (Remimazolam)
DK2802325T3 (en) 2012-01-13 2017-03-13 Massachusetts Gen Hospital ANESTHETIC RELATIONS AND RELATED APPLICATIONS THEREOF
EP2903963A4 (en) 2012-10-08 2016-05-25 Auckland Uniservices Ltd KETAMINE DERIVATIVES
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
ES2699636T3 (es) 2016-01-29 2019-02-12 Bioka S R O Nuevo procedimiento para la preparación de derivados de N-fenil-N-(4-piperidinil) amida, como remifentanilo y carfentanilo
ES2858404T3 (es) 2018-10-26 2021-09-30 Hameln Pharma Gmbh Nuevos intermedios para la preparación de clorhidrato de remifentanilo
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

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BE623427A (pt) * 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 (en) * 1987-09-25 1993-05-18 Georges H. P. Van Daele Substituted n-(1-alkyl-3-hydroxy-4-piperidinyl)benzamides

Also Published As

Publication number Publication date
NL960030I2 (nl) 1997-05-01
CZ402591A3 (en) 1993-04-14
KR0160979B1 (ko) 1998-12-01
CY2002A (en) 1997-12-05
JPH02300167A (ja) 1990-12-12
IE77156B1 (en) 1997-12-03
HK78297A (en) 1997-06-20
AU4973190A (en) 1990-08-23
PT93137B (pt) 1996-02-29
CA2010011A1 (en) 1990-08-15
ES2088961T4 (es) 1996-12-01
EP0383579A1 (en) 1990-08-22
KR900012906A (ko) 1990-09-03
MX9203024A (es) 1992-07-01
DE69027794D1 (de) 1996-08-22
GR3020719T3 (en) 1996-11-30
AU636330B2 (en) 1993-04-29
DK0383579T3 (da) 1996-10-14
DE19675028I2 (de) 2002-11-07
CA2010011C (en) 1997-12-02
ES2088961T3 (es) 1996-10-01
SG47967A1 (en) 1998-04-17
IE900532L (en) 1990-08-15
EP0383579B1 (en) 1996-07-17
ATE140451T1 (de) 1996-08-15
SK402591A3 (en) 2000-09-12
JP2895145B2 (ja) 1999-05-24
DE69027794T2 (de) 1997-01-02
NL960030I1 (nl) 1997-02-03
LU90011I2 (fr) 1997-03-11
NZ232542A (en) 1992-06-25
US5019583A (en) 1991-05-28

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Legal Events

Date Code Title Description
FG3A Patent granted, date of granting

Effective date: 19951114

PC4A Transfer of assignment

Owner name: GLAXO WELLCOME INC., US

Effective date: 20090624

Owner name: SMITHKLINE BEECHAM CORPORATION, US

Effective date: 20090624

MM4A Annulment/lapse due to non-payment of fees, searched and examined patent

Free format text: MAXIMUM VALIDITY LIMIT REACHED

Effective date: 20101115