JP2011529942A - ピリジン誘導体の結晶体 - Google Patents

ピリジン誘導体の結晶体 Download PDF

Info

Publication number
JP2011529942A
JP2011529942A JP2011521561A JP2011521561A JP2011529942A JP 2011529942 A JP2011529942 A JP 2011529942A JP 2011521561 A JP2011521561 A JP 2011521561A JP 2011521561 A JP2011521561 A JP 2011521561A JP 2011529942 A JP2011529942 A JP 2011529942A
Authority
JP
Japan
Prior art keywords
crystalline form
compound
formula
disorders
methylbenzenesulfonate
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
JP2011521561A
Other languages
English (en)
Japanese (ja)
Other versions
JP2011529942A5 (enExample
Inventor
クレア、ルイーズ、アンダートン
デイビッド、クラッパム
ロニー、マクスウェル、ローレンス
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GlaxoSmithKline LLC
Original Assignee
GlaxoSmithKline LLC
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 GlaxoSmithKline LLC filed Critical GlaxoSmithKline LLC
Publication of JP2011529942A publication Critical patent/JP2011529942A/ja
Publication of JP2011529942A5 publication Critical patent/JP2011529942A5/ja
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
JP2011521561A 2008-08-05 2009-08-04 ピリジン誘導体の結晶体 Withdrawn JP2011529942A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0814340.6A GB0814340D0 (en) 2008-08-05 2008-08-05 Anhydrous crystol form fo a pyridine derivative
GB0814340.6 2008-08-05
PCT/EP2009/060089 WO2010015626A1 (en) 2008-08-05 2009-08-04 Crystalline forms of a pyridine derivative

Publications (2)

Publication Number Publication Date
JP2011529942A true JP2011529942A (ja) 2011-12-15
JP2011529942A5 JP2011529942A5 (enExample) 2012-09-27

Family

ID=39767571

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011521561A Withdrawn JP2011529942A (ja) 2008-08-05 2009-08-04 ピリジン誘導体の結晶体

Country Status (14)

Country Link
US (1) US8093242B2 (enExample)
EP (1) EP2321324A1 (enExample)
JP (1) JP2011529942A (enExample)
KR (1) KR20110052686A (enExample)
CN (1) CN102171219A (enExample)
AU (1) AU2009279135B2 (enExample)
BR (1) BRPI0917224A2 (enExample)
CA (1) CA2733235A1 (enExample)
EA (1) EA201170300A1 (enExample)
GB (1) GB0814340D0 (enExample)
IL (1) IL210777A0 (enExample)
MX (1) MX2011001414A (enExample)
WO (1) WO2010015626A1 (enExample)
ZA (1) ZA201100426B (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2440938T3 (es) * 2009-08-27 2014-01-31 Nerre Therapeutics Limited Formas anhidrato de un derivado de piridina
AU2016264034B2 (en) * 2015-05-18 2020-03-05 KaNDy Therapeutics Limited Dual NK-1/NK-3 receptor antagonists for the treatment of sex-hormone-dependent diseases
EA202092131A1 (ru) 2018-03-14 2020-11-27 Кэнди Терапьютикс Лимитед Новый фармацевтический препарат, содержащий двойные антагонисты рецептора nk-1/nk-3
EP4058433A1 (en) * 2019-11-15 2022-09-21 KaNDy Therapeutics Limited New chemical process for making 6-chloro-4-(4-fluoro-2-methylphenyl)pyridin-3-amine a key intermediate of nt-814
WO2025242585A1 (en) 2024-05-24 2025-11-27 Bayer Consumer Care Ag Crystalline forms of salts of elinzanetant and compositions containing salts of elinzanetant
WO2025242583A1 (en) 2024-05-24 2025-11-27 Bayer Consumer Care Ag Novel formulation comprising elinzanetant in a solid dispersion
US12533358B1 (en) 2025-05-14 2026-01-27 Bayer Consumer Care Ag Methods of treatment with elinzanetant

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0912174B1 (en) 1996-07-17 2004-04-28 MERCK & CO., INC. Alteration of circadian rhythmicity with non-peptidal neurikinin-1 receptor antagonists
EP1035115B1 (en) 1999-02-24 2004-09-29 F. Hoffmann-La Roche Ag 4-Phenylpyridine derivatives and their use as NK-1 receptor antagonists
AU7788500A (en) 1999-10-25 2001-05-08 Janssen Pharmaceutica N.V. Use of substance p antagonists for influencing the circadian timing system
GB0203020D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
GB0203022D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
TW200403058A (en) * 2002-04-19 2004-03-01 Bristol Myers Squibb Co Heterocyclo inhibitors of potassium channel function
ES2291891T3 (es) * 2003-07-03 2008-03-01 F. Hoffmann-La Roche Ag Antagonistas duales de nk1/nk3 para tratamiento de esquizofrenia.
DK1928886T3 (da) * 2005-09-09 2011-07-11 Glaxosmithkline Llc Pyridin-derivater og deres anvendelse i behandlingen af psykotiske lidelser

Also Published As

Publication number Publication date
MX2011001414A (es) 2011-04-04
US8093242B2 (en) 2012-01-10
CN102171219A (zh) 2011-08-31
EP2321324A1 (en) 2011-05-18
AU2009279135B2 (en) 2012-09-13
AU2009279135A1 (en) 2010-02-11
GB0814340D0 (en) 2008-09-10
KR20110052686A (ko) 2011-05-18
ZA201100426B (en) 2012-03-28
US20110136798A1 (en) 2011-06-09
CA2733235A1 (en) 2010-02-11
BRPI0917224A2 (pt) 2015-11-24
EA201170300A1 (ru) 2011-08-30
IL210777A0 (en) 2011-03-31
WO2010015626A1 (en) 2010-02-11

Similar Documents

Publication Publication Date Title
EP4382530A1 (en) Shp2 inhibitor, pharmaceutical composition comprising same, and application thereof
JP6404186B2 (ja) 無水形態のピリジン誘導体
JP2004533446A (ja) 5,8,14−トリアザテトラシクロ[10.3.1.02,11.04,9]−ヘキサデカ−2(11),3,5,7,9−ペンタンの酒石酸塩及びその医薬組成物
CA2878006C (en) Carbamate/urea derivatives
JP2013502447A (ja) 睡眠障害の治療のためのオレキシン受容体アンタゴニストとしての5−メチル−ピペリジン誘導体
AU2009279135B2 (en) Crystalline forms of a pyridine derivative
JP5875863B2 (ja) マレイン酸オルブピタントの無水結晶形
US20120184740A1 (en) Process for the preparation of benzoimidazol-2-yl pyrimidine derivatives
CA2970388A1 (en) Nitromidazole compound, preparation method therefor and use thereof in drug manufacturing
KR20190056398A (ko) 무스카린 아세틸콜린 수용체 작용제의 결정성 다형체
TW201726686A (zh) 噻吩并嘧啶之結晶型式
JP7681113B2 (ja) テトラヒドロピロロ環化合物及びその使用
KR20200029393A (ko) 오렉신 수용체 길항제
CN118121699A (zh) Tpk激动剂及使用其治疗神经退行性疾病的方法
JP2025500049A (ja) 置換キノリン誘導体
CA3199269A1 (en) Isoxazole derivatives as modulators of the 5-ht2a serotonin receptor useful for the treatment of disorders related thereto
WO2018005732A1 (en) Half-curcuminoids as amyloid-beta pet imaging agents
WO2017058689A1 (en) Crystal forms of a m1 receptor positive allosteric modulator
CN120329280A (zh) 取代的1,2,4-四氢-3h-苯并二氮䓬-3-酮衍生物及其应用
JP2026077755A (ja) クラゾセンタン二ナトリウム塩、その製造及びそれを含有する医薬組成物
JP2014012641A (ja) 新規ピリジン誘導体

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120806

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20120806

A761 Written withdrawal of application

Free format text: JAPANESE INTERMEDIATE CODE: A761

Effective date: 20131001

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20131001