PE20001556A1 - Derivados de tetrahidropirano utiles como antagonistas de taquicinina - Google Patents

Derivados de tetrahidropirano utiles como antagonistas de taquicinina

Info

Publication number
PE20001556A1
PE20001556A1 PE2000000218A PE0002182000A PE20001556A1 PE 20001556 A1 PE20001556 A1 PE 20001556A1 PE 2000000218 A PE2000000218 A PE 2000000218A PE 0002182000 A PE0002182000 A PE 0002182000A PE 20001556 A1 PE20001556 A1 PE 20001556A1
Authority
PE
Peru
Prior art keywords
alkyl
halogen
fluoroalkyl
taquycinin
antagonists
Prior art date
Application number
PE2000000218A
Other languages
English (en)
Inventor
Brian John Williams
Eileen Mary Seward
Simon Neil Owen
Christopher John Swain
Original Assignee
Merck Sharp & Dohme
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
Priority claimed from GBGB9906480.0A external-priority patent/GB9906480D0/en
Priority claimed from GBGB9924616.7A external-priority patent/GB9924616D0/en
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of PE20001556A1 publication Critical patent/PE20001556A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • 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
    • A61P25/06Antimigraine agents
    • 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
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings 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
    • C07D309/10Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A DERIVADOS DE TETRAHIDROPIRANO DE FORMULA I, DONDE: R1 ES H, HALOGENO, ALQUILO C1-C6, NO2, CN, SRa, ENTRE OTROS; R2 ES H, HALOGENO, ALQUILO C1-C6, FLUOROALQUILO C1-C6, ENTRE OTROS; R3 ES H, HALOGENO, FLUOROALQUILO C1-C6; R4 ES H, HALOGENO, ALQUILO C1-C6, ALCOXI C1-C6, NO2, CN, SRa, CONRaRb, ENTRE OTROS; Ra Y Rb SON H, ALQUILO C1-C4; R5 ES H, HALOGENO, ALQUILO C1-C6, FLUOROALQUILO C1-C6, ENTRE OTROS; R6 ES H, ALQUILO C1-C4 OPCIONALMENTE SUSTITUIDO CON OH; R7 ES HALOGENO, OH, ALQUENILO C2-C4, N3, NR11R12, NRaCORb, ENTRE OTROS; R8 ES H, ALQUILO C1-C6, FLUOROALQUILO C1-C6, OH, ALCOXI C1-C6, HIDROXIALQUILO C1-C6; R9 Y R10 SON H, HALOGENO, ALQUILO C1-C6, CH2ORc, OXO, CO2Ra, CONRaRb; Rc ES H, ALQUILO C1-C6, FENILO; R11 ES H, ALQUILO C1-C4, CICLOALQUILO C3-C7, ENTRE OTROS; R12 ES H, ALQUILO C1-C4, CICLOALQUILO C3-C7, ALQUILO C1-C4, ENTRE OTROS; n ES 0-2. UN COMPUESTOS PREFERIDO ES (2R,3S,4S,8R)-2-(1-(1-(3,5-BIS(TRIFLUOROMETIL)FENIL)ETIL)OXI)-4-(METANOSULFONILOXI)METIL-3-FENILTETRAHIDROPIRANO, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. EL COMPUESTO DE FORMULA I ES UN ANTAGONISTA DEL RECEPTOR DE TAQUICININA DE PREFERENCIA NEUROCININA 1 (NK-1) Y PUEDE SER UTIL PARA EL TRATAMIENTO DE TRASTORNOS DEL SISTEMA NERVIOSO CENTRAL, DEPRESION, ANSIEDAD, PREVENCION DEL DOLOR, INFLAMACION
PE2000000218A 1999-03-19 2000-03-13 Derivados de tetrahidropirano utiles como antagonistas de taquicinina PE20001556A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9906480.0A GB9906480D0 (en) 1999-03-19 1999-03-19 Therapeutic agents
GBGB9924616.7A GB9924616D0 (en) 1999-10-18 1999-10-18 Therapeutic agents

Publications (1)

Publication Number Publication Date
PE20001556A1 true PE20001556A1 (es) 2001-01-13

Family

ID=26315315

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2000000218A PE20001556A1 (es) 1999-03-19 2000-03-13 Derivados de tetrahidropirano utiles como antagonistas de taquicinina

Country Status (23)

Country Link
US (1) US6458830B1 (es)
EP (1) EP1165540B1 (es)
JP (1) JP2002540107A (es)
KR (1) KR20010113773A (es)
CN (1) CN1344264A (es)
AT (1) ATE247096T1 (es)
AU (2) AU746251B2 (es)
BG (1) BG105859A (es)
BR (1) BR0009127A (es)
CA (1) CA2367985A1 (es)
CO (1) CO5150225A1 (es)
CZ (1) CZ20013377A3 (es)
DE (1) DE60004504T2 (es)
EA (1) EA200100902A1 (es)
EE (1) EE200100491A (es)
ES (1) ES2203434T3 (es)
HU (1) HUP0200441A3 (es)
IL (1) IL144236A0 (es)
NO (1) NO20014529L (es)
PE (1) PE20001556A1 (es)
PL (1) PL350123A1 (es)
SK (1) SK13322001A3 (es)
WO (2) WO2000056727A1 (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10001785A1 (de) * 2000-01-18 2001-07-19 Boehringer Ingelheim Pharma NK¶1¶-Rezeptor-Antagonisten zur Behandlung des Restless Legs Syndroms
GB0017256D0 (en) 2000-07-13 2000-08-30 Merck Sharp & Dohme Therapeutic agents
GB0020721D0 (en) 2000-08-22 2000-10-11 Merck Sharp & Dohme Therapeutic agents
PE20020444A1 (es) 2000-09-22 2002-06-14 Merck & Co Inc Antagonistas de receptores de taquiquinina zwitterionica
US6906085B2 (en) 2001-01-17 2005-06-14 Merck Sharp & Dohme Ltd. Tetrahydropyran derivatives as neurokinin receptor antagonists
GB0121874D0 (en) * 2001-09-10 2001-10-31 Merck Sharp & Dohme Therapeutic agents
GB0217068D0 (en) * 2002-07-23 2002-08-28 Merck Sharp & Dohme Therapeutic agents
EP1562975A2 (en) * 2002-10-25 2005-08-17 Yissum Research Development Company Of The Hebrew University Of Jerusalem Steroid compounds comprising superoxide dismutase mimic groups and nitric oxide donor groups, and their use in the preparation of medicaments
AU2003286389A1 (en) * 2002-11-29 2004-06-23 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ace-inhibitors having antioxidant and nitricoxid-donor activity
JP2006519822A (ja) * 2003-03-07 2006-08-31 メルク シャープ エンド ドーム リミテッド タキキニン拮抗薬としてのテトラヒドロピラン化合物
US7589205B2 (en) * 2004-09-08 2009-09-15 Nycomed Gmbh 3-thia-10-aza-phenanthrene derivatives
JP2008521804A (ja) * 2004-11-30 2008-06-26 マリンクロッド・インコーポレイテッド ベンズフェタミンの結晶化方法
CA2605594A1 (en) * 2005-04-22 2006-11-02 Daiichi Sankyo Company, Limited Heterocyclic compound
CN100395242C (zh) * 2006-06-08 2008-06-18 华东理工大学 烷氧基萘和萘醌类吡喃碳糖苷化合物及其制备方法
DE102007010077B4 (de) * 2007-02-28 2010-04-08 RUHR-UNIVERSITäT BOCHUM [1,3]-Dioxane zur Modulation von GABAa-Rezeptoren
US9782397B2 (en) 2011-07-04 2017-10-10 Irbm Science Park S.P.A. Treatment of corneal neovascularization
CA2883791A1 (en) * 2012-09-04 2014-03-13 Lauren Sciences Llc Bolaamphiphilic compounds, compositions and uses thereof
MX2016015610A (es) 2014-06-06 2017-07-13 Flexus Biosciences Inc Agentes inmunorreguladores.
EP3215141A4 (en) 2014-11-05 2018-06-06 Flexus Biosciences, Inc. Immunoregulatory agents
UY36391A (es) 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido1), sus métodos de síntesis y composiciones farmacèuticas que las contienen
UY36390A (es) 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen
HU231150B1 (hu) 2017-03-13 2021-03-29 Richter Gedeon Nyrt Eljárás racém 3-alkilpiperidin-3-karbonsav-etil-észterek optikai izomerjeinek elválasztására
WO2019156074A1 (ja) * 2018-02-06 2019-08-15 第一三共株式会社 アミノアルキル化合物
CN111918647A (zh) 2018-02-26 2020-11-10 圣拉斐尔医院有限公司 用于治疗眼痛的nk-1拮抗剂
US20230134843A1 (en) 2020-03-11 2023-05-04 Ospedale San Raffaele S.R.L. Treatment of stem cell deficiency

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9301920D0 (en) * 1993-02-01 1993-03-17 Foundation For Ethnobiology Th Polycetylenes

Also Published As

Publication number Publication date
EA200100902A1 (ru) 2002-02-28
DE60004504D1 (de) 2003-09-18
CA2367985A1 (en) 2000-09-28
DE60004504T2 (de) 2004-06-24
BG105859A (bg) 2002-04-30
EP1165540B1 (en) 2003-08-13
CO5150225A1 (es) 2002-04-29
HUP0200441A2 (hu) 2002-07-29
NO20014529L (no) 2001-11-13
WO2000056727A1 (en) 2000-09-28
US6458830B1 (en) 2002-10-01
AU746251B2 (en) 2002-04-18
SK13322001A3 (sk) 2002-02-05
WO2000056728A1 (en) 2000-09-28
AU3304200A (en) 2000-10-09
NO20014529D0 (no) 2001-09-18
KR20010113773A (ko) 2001-12-28
EE200100491A (et) 2002-12-16
CN1344264A (zh) 2002-04-10
BR0009127A (pt) 2001-12-26
ES2203434T3 (es) 2004-04-16
IL144236A0 (en) 2002-05-23
EP1165540A1 (en) 2002-01-02
CZ20013377A3 (cs) 2002-02-13
HUP0200441A3 (en) 2002-09-30
JP2002540107A (ja) 2002-11-26
ATE247096T1 (de) 2003-08-15
AU3304400A (en) 2000-10-09
PL350123A1 (en) 2002-11-04

Similar Documents

Publication Publication Date Title
PE20001556A1 (es) Derivados de tetrahidropirano utiles como antagonistas de taquicinina
MA27190A1 (fr) Derives de tropane servant de modulateurs de ccr5
RU2437882C2 (ru) Производные имидазолидинона
DE60025189D1 (de) Cyanopyrrole als progesteronrezeptoragonisten
PE20010854A1 (es) USO DE DERIVADOS DE PIRIMIDINA 4 SUSTITUIDOS COMO ANTAGONISTAS DE LOS RECEPTORES DE GLUTAMATO mGluR1
PE20000166A1 (es) Compuestos 4-(2-ceto-1-benzilimidazolinil)piperidina como agonistas del receptor orl1
PE20011114A1 (es) Decahidro-isoquinolinas
PE20010930A1 (es) Bifenil sulfonamidas como antagonistas de receptores de angiotensina endotelina duales
PE20011119A1 (es) Composiciones farmaceuticas de agonista/antagonista de estrogenos para el tratamiento de afecciones que responden a un aumento de testosterona
DE69223989T2 (de) Azyklische ethylendiaminderivate als 'substance p rezeptor' antagonisten
PE20010741A1 (es) Derivados de piperazina como antagonistas de taquicininas
PE20030238A1 (es) Uso de los antagonistas del receptor nk-1 para el tratamiento de lesiones cerebrales, espinales y neuronales
DE69709624D1 (de) Chinazolinverbindungen
RU98108027A (ru) Производные имидазола, обладающие аффинностью в отношении активности альфа2- рецепторов
PE20011068A1 (es) 1,3-pirrolidinas disustituidas
PE20041061A1 (es) Imidazol-4-il-etinil-piridina
RU2007137266A (ru) Хиназолиноновые антагонисты кальциевых каналов т-типа
PE20060632A1 (es) Derivados de arilsulfonilestilbeno como antagonistas de los receptores 5-ht2a
PE20070069A1 (es) Piperazin-piperidinas como antagonistas y agonistas del receptor 5-ht1a
PE20081315A1 (es) Derivados de benzimidazol como antagonistas de vr-1
DE59707062D1 (de) 2,3-benzodiazepinderivate und deren verwendung als ampa-rezeptoren-hemmer
DK1189900T3 (da) Heterocykliske aminopyrrolidinderivater som melatonerge lægemidler
RU2005117374A (ru) Индолы, полезные для лечения заболеваний, связанных с андрогеновыми рецепторами
AR005916A1 (es) Compuestos de oxadiazol, y de tiadiazol, su uso, procedimientos para prepararlos, composiciones farmaceuticas que los contienen y un compuesto util como intermedio
PE20020436A1 (es) Derivados de tetrahidropirano como antagonistas del receptor de neuroquinina 1 (nk-1)

Legal Events

Date Code Title Description
FD Application declared void or lapsed