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AR054745A1 - Proceso para la preparacion de moduladores opioides - Google Patents

Proceso para la preparacion de moduladores opioides

Info

Publication number
AR054745A1
AR054745A1 ARP060100973A ARP060100973A AR054745A1 AR 054745 A1 AR054745 A1 AR 054745A1 AR P060100973 A ARP060100973 A AR P060100973A AR P060100973 A ARP060100973 A AR P060100973A AR 054745 A1 AR054745 A1 AR 054745A1
Authority
AR
Argentina
Prior art keywords
formula
compound
give
reacting
corresponding compound
Prior art date
Application number
ARP060100973A
Other languages
English (en)
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=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR054745(A1) "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 AR054745A1 publication Critical patent/AR054745A1/es

Links

Classifications

    • 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
    • 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
    • C07D233/64Heterocyclic 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (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)

Abstract

Reivindicacion 1: Un proceso para la preparacion de un compuesto de formula (1) en la cual el anillo P es arilo C6-10 o un heteroarilo seleccionado del grupo integrado por furilo, tienilo, pirrolilo, oxazolilo, tiazolilo, imidazolilo, pirazolilo, piridinilo, pirimidinilo, pirazinilo, indolilo, isoindolilo, indolinilo, benzofurilo, benzotienilo, bencimidazolilo, benzotiazolilo, benzoxazolilo, quinolizinilo, quinolinilo, isoquinolinilo y quinazolinilo; cada R41p se selecciona independientemente de alquilo C1-6, alcoxi C1-6 o F; RJ y RK se seleccionan cada uno independientemente de H o alquilo C1-4; en forma alternativa, RJ y RK se toman junto con el átomo de N al cual están unidos para formar un heterociclilo de 5 a 7 miembros; Pg1 es un grupo protector de N; que comprende hacer reaccionar un compuesto de formula (2), en la cual Xp se selecciona de OH, CN, -CO2H, -C(O)-CL o -C(O)-Oalquilo C1-4 y en la cual Yp se selecciona de Br, Cl, o I, para dar el compuesto correspondiente de formula (3); hacer reaccionar el compuesto de formula (3) con un compuesto sustituido en forma adecuada de formula (4); en presencia de un catalizador de paladio; en presencia de una base orgánica o inorgánica; en un solvente orgánico; a una temperatura superior aproximadamente la temperatura ambiente; para dar el compuesto correspondiente de formula (5); hacer reaccionar el compuesto de formula (5) con H o una fuente de H, en presencia de un catalizador; en un solvente, a una temperatura superior a aproximadamente la temperatura ambiente; para dar el compuesto correspondiente de formula (6); hacer reaccionar el compuesto de formula (6) con una base acuosa; en un solvente orgánico, para dar el compuesto correspondiente de formula (1).
ARP060100973A 2005-03-14 2006-03-14 Proceso para la preparacion de moduladores opioides AR054745A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US66178405P 2005-03-14 2005-03-14
US11/368,588 US20060211861A1 (en) 2005-03-14 2006-03-06 Process for the preparation of opioid modulators

Publications (1)

Publication Number Publication Date
AR054745A1 true AR054745A1 (es) 2007-07-11

Family

ID=36646011

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP060100973A AR054745A1 (es) 2005-03-14 2006-03-14 Proceso para la preparacion de moduladores opioides
ARP060100974A AR053170A1 (es) 2005-03-14 2006-03-14 Proceso para la preparacion de moduladores de receptores opioides e intermediarios en su sintesis

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP060100974A AR053170A1 (es) 2005-03-14 2006-03-14 Proceso para la preparacion de moduladores de receptores opioides e intermediarios en su sintesis

Country Status (30)

Country Link
US (4) US20060211861A1 (es)
EP (2) EP1858850B1 (es)
JP (3) JP2008533141A (es)
KR (2) KR101280929B1 (es)
CN (2) CN101175725B (es)
AR (2) AR054745A1 (es)
AU (2) AU2006223482A1 (es)
BR (2) BRPI0607792A2 (es)
CA (2) CA2601481C (es)
CR (1) CR9438A (es)
CY (1) CY1116104T1 (es)
DK (1) DK1858850T3 (es)
EA (2) EA014366B1 (es)
ES (1) ES2535048T3 (es)
HR (1) HRP20150417T1 (es)
HU (1) HUE024912T2 (es)
IL (3) IL185974A0 (es)
ME (1) ME02110B (es)
MX (2) MX2007011412A (es)
MY (1) MY145333A (es)
NI (1) NI200700237A (es)
NO (2) NO20075268L (es)
NZ (1) NZ590570A (es)
PL (1) PL1858850T3 (es)
PT (1) PT1858850E (es)
RS (1) RS53873B1 (es)
SI (1) SI1858850T1 (es)
TW (3) TWI414518B (es)
WO (2) WO2006099060A2 (es)
ZA (2) ZA200708809B (es)

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
CN1950342B (zh) * 2004-03-15 2012-09-26 詹森药业有限公司 作为阿片受体调节剂的新化合物
DK1858850T3 (en) * 2005-03-14 2015-02-09 Janssen Pharmaceutica Nv PROCEDURE FOR THE MANUFACTURING OF OPIOID MODULATORS
UA104713C2 (ru) * 2007-07-09 2014-03-11 Фуриекс Фармасьютикалз, Инк. Кристаллы и способ получения 5-({[2-амино-3-(4-карбамоил-2,6-диметилфенил)-пропионил]-[1-(4-фенил-1h-имидазол-2-ил)-этил]-амино}-метил)-метоксибензойной кислоты
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
CN108026032B (zh) * 2015-09-11 2020-09-29 株式会社钟化 光学活性4-氨基甲酰基-2,6-二甲基苯基丙氨酸衍生物的制造方法
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
US10822308B2 (en) * 2016-06-23 2020-11-03 Sun Pharmaceutical Industries Limited Processes for the preparation of eluxadoline
WO2018047131A1 (en) * 2016-09-09 2018-03-15 Sun Pharmaceutical Industries Limited Amorphous eluxadoline
WO2018055528A2 (en) 2016-09-20 2018-03-29 Sun Pharmaceutical Industries Limited Processes for the preparation of eluxadoline
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
WO2018138272A1 (en) 2017-01-27 2018-08-02 Quimica Sintetica, S. A. Eluxadoline crystalline form and process for the preparation thereof
US10738013B2 (en) 2017-01-27 2020-08-11 Quimica Sintetica, S.A. Eluxadoline crystalline forms and processes for their preparation
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
CN115298173A (zh) 2020-03-31 2022-11-04 田边三菱制药株式会社 羟基吡咯烷衍生物及其医药用途
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
WO1996022997A1 (en) * 1995-01-27 1996-08-01 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
CA2322873A1 (en) * 1998-03-11 1999-09-16 G.D. Searle & Co. Halogenated amidino amino acid derivatives useful as nitric oxide synthase inhibitors
ES2206139T3 (es) * 1999-05-28 2004-05-16 Pfizer Products Inc. Derivados de 3-(3-hidrofenil)-3-amino-propionamida.
NZ525928A (en) * 2000-10-30 2005-06-24 Janssen Pharmaceutica Nv Tripeptidyl peptidase inhibitors
US7041681B2 (en) * 2002-04-29 2006-05-09 Janssen Pharmaceutica N.V. Compounds as opioid receptor modulators
CN1950342B (zh) * 2004-03-15 2012-09-26 詹森药业有限公司 作为阿片受体调节剂的新化合物
DK1858850T3 (en) * 2005-03-14 2015-02-09 Janssen Pharmaceutica Nv PROCEDURE FOR THE MANUFACTURING OF OPIOID MODULATORS

Also Published As

Publication number Publication date
ES2535048T3 (es) 2015-05-04
PL1858850T3 (pl) 2015-06-30
EP1863764A1 (en) 2007-12-12
IL185972A (en) 2013-07-31
TW201302676A (zh) 2013-01-16
CN101175726A (zh) 2008-05-07
MY145333A (en) 2012-01-31
CA2601481A1 (en) 2006-09-21
CA2601481C (en) 2013-11-12
BRPI0607793A2 (pt) 2009-06-13
US7629488B2 (en) 2009-12-08
KR20070116067A (ko) 2007-12-06
IL209402A0 (en) 2011-01-31
HUE024912T2 (en) 2016-02-29
JP2013234192A (ja) 2013-11-21
MX2007011412A (es) 2008-02-22
EP1858850B1 (en) 2015-01-21
TW200716548A (en) 2007-05-01
BRPI0607792A2 (pt) 2009-06-13
DK1858850T3 (en) 2015-02-09
EA200701978A1 (ru) 2008-04-28
HRP20150417T1 (xx) 2015-09-25
PT1858850E (pt) 2015-02-24
US20100036132A1 (en) 2010-02-11
IL185972A0 (en) 2008-01-06
CA2601674A1 (en) 2006-09-21
ZA200708809B (en) 2009-03-25
JP2008533143A (ja) 2008-08-21
IL185974A0 (en) 2008-01-06
NO20075268L (no) 2007-12-10
CN101175725B (zh) 2011-02-02
TW200700388A (en) 2007-01-01
AU2006223394A1 (en) 2006-09-21
EP1858850A2 (en) 2007-11-28
US20060211863A1 (en) 2006-09-21
EA014366B1 (ru) 2010-10-29
US20060211861A1 (en) 2006-09-21
NO340604B1 (no) 2017-05-15
EA200701979A1 (ru) 2008-04-28
ME02110B (me) 2015-10-20
NO20075269L (no) 2007-12-10
MX2007011409A (es) 2008-02-22
US20100152460A1 (en) 2010-06-17
KR20070112255A (ko) 2007-11-22
CY1116104T1 (el) 2017-02-08
TWI414518B (zh) 2013-11-11
IL209402A (en) 2015-06-30
WO2006098982A1 (en) 2006-09-21
WO2006099060A2 (en) 2006-09-21
SI1858850T1 (sl) 2015-04-30
RS53873B1 (sr) 2015-08-31
CN101175725A (zh) 2008-05-07
NI200700237A (es) 2008-06-25
CR9438A (es) 2008-09-09
TWI500595B (zh) 2015-09-21
EA015512B1 (ru) 2011-08-30
KR101280929B1 (ko) 2013-07-01
NZ590570A (en) 2012-06-29
JP5802242B2 (ja) 2015-10-28
JP5384933B2 (ja) 2014-01-08
AU2006223394B2 (en) 2012-10-18
AU2006223482A1 (en) 2006-09-21
JP2008533141A (ja) 2008-08-21
ZA200708810B (en) 2009-01-28
WO2006099060A3 (en) 2006-11-02
AR053170A1 (es) 2007-04-25

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