TW200700388A - Process for the preparation of opioid modulators - Google Patents

Process for the preparation of opioid modulators

Info

Publication number
TW200700388A
TW200700388A TW095108513A TW95108513A TW200700388A TW 200700388 A TW200700388 A TW 200700388A TW 095108513 A TW095108513 A TW 095108513A TW 95108513 A TW95108513 A TW 95108513A TW 200700388 A TW200700388 A TW 200700388A
Authority
TW
Taiwan
Prior art keywords
preparation
opioid modulators
opioid
modulators
agonists
Prior art date
Application number
TW095108513A
Other languages
English (en)
Inventor
chao-zhong Cai
Wei He
Original Assignee
Janssen Pharmaceutica Nv
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=36646011&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TW200700388(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of TW200700388A publication Critical patent/TW200700388A/zh

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
    • C07D211/36Heterocyclic 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/10Laxatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C07C233/11Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/14Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being saturated and containing rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
    • C07D217/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/61Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
TW095108513A 2005-03-14 2006-03-14 Process for the preparation of opioid modulators TW200700388A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US66178405P 2005-03-14 2005-03-14
US11/368,564 US7629488B2 (en) 2005-03-14 2006-03-06 Process for the preparation of opioid modulators

Publications (1)

Publication Number Publication Date
TW200700388A true TW200700388A (en) 2007-01-01

Family

ID=36646011

Family Applications (3)

Application Number Title Priority Date Filing Date
TW101129655A TWI500595B (zh) 2005-03-14 2006-03-14 製備類鴉片調節劑之方法(一)
TW095108513A TW200700388A (en) 2005-03-14 2006-03-14 Process for the preparation of opioid modulators
TW095108512A TWI414518B (zh) 2005-03-14 2006-03-14 製備類鴉片調節劑之方法(一)

Family Applications Before (1)

Application Number Title Priority Date Filing Date
TW101129655A TWI500595B (zh) 2005-03-14 2006-03-14 製備類鴉片調節劑之方法(一)

Family Applications After (1)

Application Number Title Priority Date Filing Date
TW095108512A TWI414518B (zh) 2005-03-14 2006-03-14 製備類鴉片調節劑之方法(一)

Country Status (30)

Country Link
US (4) US7629488B2 (zh)
EP (2) EP1863764A1 (zh)
JP (3) JP5384933B2 (zh)
KR (2) KR101280929B1 (zh)
CN (2) CN101175726A (zh)
AR (2) AR054745A1 (zh)
AU (2) AU2006223482A1 (zh)
BR (2) BRPI0607793A2 (zh)
CA (2) CA2601481C (zh)
CR (1) CR9438A (zh)
CY (1) CY1116104T1 (zh)
DK (1) DK1858850T3 (zh)
EA (2) EA014366B1 (zh)
ES (1) ES2535048T3 (zh)
HR (1) HRP20150417T1 (zh)
HU (1) HUE024912T2 (zh)
IL (3) IL185972A (zh)
ME (1) ME02110B (zh)
MX (2) MX2007011412A (zh)
MY (1) MY145333A (zh)
NI (1) NI200700237A (zh)
NO (2) NO340604B1 (zh)
NZ (1) NZ590570A (zh)
PL (1) PL1858850T3 (zh)
PT (1) PT1858850E (zh)
RS (1) RS53873B1 (zh)
SI (1) SI1858850T1 (zh)
TW (3) TWI500595B (zh)
WO (2) WO2006099060A2 (zh)
ZA (2) ZA200708809B (zh)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7041681B2 (en) * 2002-04-29 2006-05-09 Janssen Pharmaceutica N.V. Compounds as opioid receptor modulators
TWI361069B (en) * 2004-03-15 2012-04-01 Janssen Pharmaceutica Nv Novel compounds as opioid receptor modulators
MX2007011412A (es) * 2005-03-14 2008-02-22 Johnson & Johnson Procedimiento para la preparacion de moduladores de opioide.
CN101730685A (zh) 2007-07-09 2010-06-09 詹森药业有限公司 5-({[2-氨基-3-(4-氨甲酰基-2,6-二甲基-苯基)-丙酰基]-[1-(4-苯基-1h-咪唑-2-基)-乙基]-氨基}-甲基)-2-甲氧基-苯甲酸的新型晶体及其制备方法
TWI468375B (zh) * 2008-10-27 2015-01-11 Janssen Pharmaceutica Nv 製備經保護之l-丙胺酸衍生物之方法
IS2977B (is) 2015-02-23 2017-07-15 Actavis Group Ptc Ehf. Aðferð til framleiðslu á milliefnum sem eru nytsamleg við nýsmíði á elúxadólíni
WO2017043626A1 (ja) * 2015-09-11 2017-03-16 株式会社カネカ 光学活性4-カルバモイル-2,6-ジメチルフェニルアラニン誘導体の製造法
CN105777584B (zh) * 2016-03-28 2018-01-02 成都伊诺达博医药科技有限公司 丙氨酸衍生物的制备方法
CN105693554B (zh) * 2016-04-06 2017-08-08 成都伊诺达博医药科技有限公司 丙氨酸衍生物的制备方法
EP3474847B1 (en) * 2016-06-23 2022-09-07 Sun Pharmaceutical Industries Limited Processes for the preparation of eluxadoline
WO2018047131A1 (en) * 2016-09-09 2018-03-15 Sun Pharmaceutical Industries Limited Amorphous eluxadoline
EP3515434A4 (en) 2016-09-20 2020-02-26 Sun Pharmaceutical Industries Limited METHOD FOR PRODUCING ELUXADOLIN
CN106866463B (zh) * 2017-01-24 2018-08-28 富乐马鸿凯(大连)医药有限公司 艾沙度林中间体的制备方法
US10738013B2 (en) 2017-01-27 2020-08-11 Quimica Sintetica, S.A. Eluxadoline crystalline forms and processes for their preparation
WO2018138272A1 (en) 2017-01-27 2018-08-02 Quimica Sintetica, S. A. Eluxadoline crystalline form and process for the preparation thereof
CN111377832A (zh) * 2018-12-27 2020-07-07 江苏联昇化学有限公司 一种伊卢多啉中间体制备的新方法
WO2021201036A1 (ja) 2020-03-31 2021-10-07 田辺三菱製薬株式会社 ヒドロキシピロリジン誘導体およびその医薬用途
CN114163348A (zh) * 2020-11-27 2022-03-11 成都泰蓉生物科技有限公司 一种氨酰基取代的l-苯丙氨酸的合成方法
CN114507252B (zh) * 2022-02-21 2023-10-27 广西大学 新型芳基硅烷化合物的合成方法

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5430129A (en) * 1977-08-09 1979-03-06 Mitsubishi Gas Chem Co Inc Preparation of toluic acid amide
JPS5528959A (en) * 1978-08-22 1980-02-29 Sumitomo Chem Co Ltd Production of amide derivative
FR2584401B1 (fr) * 1985-07-04 1987-11-20 Ile De France Nouveau benzamide, son procede de preparation et son application dans le domaine therapeutique
JP2727243B2 (ja) * 1988-12-27 1998-03-11 日本化薬株式会社 2−アシルアミノ桂皮酸誘導体の製造法
US5684175A (en) * 1993-02-05 1997-11-04 Napro Biotherapeutics, Inc. C-2' hydroxyl-benzyl protected, N-carbamate protected (2R, 3S)- 3-phenylisoserine and production process therefor
JP3493206B2 (ja) * 1993-03-19 2004-02-03 ダイセル化学工業株式会社 光学活性β−アミノ酸類の製法
JP3486922B2 (ja) * 1993-08-23 2004-01-13 住友化学工業株式会社 酸アミドの製造法
EP0805816B1 (en) * 1995-01-27 2004-07-28 Novo Nordisk A/S Compounds with growth hormone releasing properties
JPH09295939A (ja) * 1995-09-26 1997-11-18 Takeda Chem Ind Ltd リン酸アミド誘導体、その製造法および用途
GEP20043179B (en) * 1998-03-11 2004-02-25 Searle & Co Halogenated Amidino Amino Acid Derivatives Useful as Nitric Oxide Synthase Inhibitors
EP1055665B1 (en) * 1999-05-28 2003-10-22 Pfizer Products Inc. 3-(3-Hydroxyphenyl)-3-amino-propionamide derivatives
CA2422617C (en) * 2000-10-30 2011-07-12 Janssen Pharmaceutica N.V. Tripeptidyl peptidase inhibitors
US7041681B2 (en) * 2002-04-29 2006-05-09 Janssen Pharmaceutica N.V. Compounds as opioid receptor modulators
TWI361069B (en) * 2004-03-15 2012-04-01 Janssen Pharmaceutica Nv Novel compounds as opioid receptor modulators
MX2007011412A (es) * 2005-03-14 2008-02-22 Johnson & Johnson Procedimiento para la preparacion de moduladores de opioide.

Also Published As

Publication number Publication date
PL1858850T3 (pl) 2015-06-30
IL209402A0 (en) 2011-01-31
ZA200708810B (en) 2009-01-28
JP2013234192A (ja) 2013-11-21
WO2006099060A3 (en) 2006-11-02
CY1116104T1 (el) 2017-02-08
US20100036132A1 (en) 2010-02-11
SI1858850T1 (sl) 2015-04-30
CN101175725A (zh) 2008-05-07
CN101175726A (zh) 2008-05-07
KR101280929B1 (ko) 2013-07-01
NO340604B1 (no) 2017-05-15
EA015512B1 (ru) 2011-08-30
CA2601481C (en) 2013-11-12
JP5802242B2 (ja) 2015-10-28
JP2008533141A (ja) 2008-08-21
KR20070116067A (ko) 2007-12-06
ME02110B (me) 2015-10-20
ZA200708809B (en) 2009-03-25
US20060211863A1 (en) 2006-09-21
EP1863764A1 (en) 2007-12-12
MX2007011412A (es) 2008-02-22
CA2601481A1 (en) 2006-09-21
AU2006223394A1 (en) 2006-09-21
ES2535048T3 (es) 2015-05-04
PT1858850E (pt) 2015-02-24
AR054745A1 (es) 2007-07-11
US20060211861A1 (en) 2006-09-21
TW201302676A (zh) 2013-01-16
EP1858850A2 (en) 2007-11-28
NZ590570A (en) 2012-06-29
CR9438A (es) 2008-09-09
US7629488B2 (en) 2009-12-08
MY145333A (en) 2012-01-31
MX2007011409A (es) 2008-02-22
CA2601674A1 (en) 2006-09-21
WO2006098982A1 (en) 2006-09-21
TW200716548A (en) 2007-05-01
TWI414518B (zh) 2013-11-11
KR20070112255A (ko) 2007-11-22
AU2006223482A1 (en) 2006-09-21
DK1858850T3 (en) 2015-02-09
NI200700237A (es) 2008-06-25
IL209402A (en) 2015-06-30
TWI500595B (zh) 2015-09-21
NO20075268L (no) 2007-12-10
JP2008533143A (ja) 2008-08-21
RS53873B1 (en) 2015-08-31
BRPI0607793A2 (pt) 2009-06-13
JP5384933B2 (ja) 2014-01-08
HUE024912T2 (en) 2016-02-29
EA200701979A1 (ru) 2008-04-28
IL185972A0 (en) 2008-01-06
EP1858850B1 (en) 2015-01-21
NO20075269L (no) 2007-12-10
EA014366B1 (ru) 2010-10-29
IL185974A0 (en) 2008-01-06
AR053170A1 (es) 2007-04-25
US20100152460A1 (en) 2010-06-17
CN101175725B (zh) 2011-02-02
EA200701978A1 (ru) 2008-04-28
IL185972A (en) 2013-07-31
HRP20150417T1 (en) 2015-09-25
WO2006099060A2 (en) 2006-09-21
AU2006223394B2 (en) 2012-10-18
BRPI0607792A2 (pt) 2009-06-13

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