UA72890C2 - A crystalline form of osanetant (variants), a method for the preparation thereof (variants) and a pharmaceutical composition - Google Patents

A crystalline form of osanetant (variants), a method for the preparation thereof (variants) and a pharmaceutical composition

Info

Publication number
UA72890C2
UA72890C2 UA2001010591A UA2001010591A UA72890C2 UA 72890 C2 UA72890 C2 UA 72890C2 UA 2001010591 A UA2001010591 A UA 2001010591A UA 2001010591 A UA2001010591 A UA 2001010591A UA 72890 C2 UA72890 C2 UA 72890C2
Authority
UA
Ukraine
Prior art keywords
variants
osanetant
preparation
pharmaceutical composition
crystalline form
Prior art date
Application number
UA2001010591A
Other languages
English (en)
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Publication of UA72890C2 publication Critical patent/UA72890C2/xx

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
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
UA2001010591A 1998-08-05 1999-08-03 A crystalline form of osanetant (variants), a method for the preparation thereof (variants) and a pharmaceutical composition UA72890C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9810107A FR2782082B3 (fr) 1998-08-05 1998-08-05 Formes cristallines de (r)-(+)-n-[[3-[1-benzoyl-3-(3,4- dichlorophenyl)piperidin-3-yl]prop-1-yl]-4-phenylpiperidin-4 -yl]-n-methylacetamide (osanetant) et procede pour la preparation dudit compose
PCT/FR1999/001914 WO2000007987A1 (fr) 1998-08-05 1999-08-03 Formes cristallines du osanetant

Publications (1)

Publication Number Publication Date
UA72890C2 true UA72890C2 (en) 2005-05-16

Family

ID=9529458

Family Applications (1)

Application Number Title Priority Date Filing Date
UA2001010591A UA72890C2 (en) 1998-08-05 1999-08-03 A crystalline form of osanetant (variants), a method for the preparation thereof (variants) and a pharmaceutical composition

Country Status (31)

Country Link
US (1) US7041679B2 (de)
EP (1) EP1102747B1 (de)
JP (1) JP3807938B2 (de)
KR (1) KR100571944B1 (de)
CN (1) CN1114592C (de)
AR (1) AR019953A1 (de)
AT (1) ATE243197T1 (de)
AU (1) AU748177B2 (de)
BR (1) BR9913357A (de)
CA (1) CA2339007A1 (de)
CO (1) CO5070576A1 (de)
DE (1) DE69908951T2 (de)
DK (1) DK1102747T3 (de)
DZ (1) DZ3074A1 (de)
EA (1) EA003205B1 (de)
EE (1) EE04274B1 (de)
ES (1) ES2200535T3 (de)
FR (1) FR2782082B3 (de)
HU (1) HUP0103134A3 (de)
IS (1) IS5821A (de)
MY (1) MY121447A (de)
NO (1) NO320645B1 (de)
NZ (1) NZ509561A (de)
PL (1) PL345999A1 (de)
PT (1) PT1102747E (de)
SK (1) SK1742001A3 (de)
TR (1) TR200100261T2 (de)
TW (1) TW527354B (de)
UA (1) UA72890C2 (de)
WO (1) WO2000007987A1 (de)
YU (1) YU8601A (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0100902D0 (sv) 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0202539D0 (sv) 2002-08-27 2002-08-27 Astrazeneca Ab Compounds
US7648992B2 (en) * 2004-07-05 2010-01-19 Astrazeneca Ab Hydantoin derivatives for the treatment of obstructive airway diseases
SE0401762D0 (sv) * 2004-07-05 2004-07-05 Astrazeneca Ab Novel compounds
SE0403085D0 (sv) * 2004-12-17 2004-12-17 Astrazeneca Ab Novel componds
SE0403086D0 (sv) * 2004-12-17 2004-12-17 Astrazeneca Ab Compounds
TW200800954A (en) * 2006-03-16 2008-01-01 Astrazeneca Ab Novel crystal modifications
TW200831488A (en) * 2006-11-29 2008-08-01 Astrazeneca Ab Novel compounds
US20240336565A1 (en) * 2021-07-02 2024-10-10 Acer Therapeutics, Inc. Solid forms of osanetant

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2719311B1 (fr) 1994-03-18 1998-06-26 Sanofi Sa Composés antagonistes sélectifs du récepteur NK3 humain et leur utilisation comme médicaments et outils de diagnostic.
JPH1053576A (ja) * 1996-06-07 1998-02-24 Eisai Co Ltd 塩酸ドネペジルの多形結晶およびその製造法
EP0915849A2 (de) * 1996-08-05 1999-05-19 Smithkline Beecham S.p.A. Verfahren zur herstellung von 3,3-disubstituierten piperidinen
US6040316A (en) * 1996-09-16 2000-03-21 Warner-Lambert Company 3-alkyl-3-phenyl-piperidines
FR2757543B1 (fr) * 1996-12-23 1999-04-02 Sanofi Sa Procede pour la cristallisation d'un derive de tetrahydropyridine et formes cristallines ainsi obtenues

Also Published As

Publication number Publication date
MY121447A (en) 2006-01-28
EE200100070A (et) 2002-06-17
KR100571944B1 (ko) 2006-04-18
CN1314888A (zh) 2001-09-26
JP3807938B2 (ja) 2006-08-09
EA200100096A1 (ru) 2001-08-27
HUP0103134A3 (en) 2003-03-28
SK1742001A3 (en) 2001-11-06
DK1102747T3 (da) 2003-09-29
ES2200535T3 (es) 2004-03-01
TW527354B (en) 2003-04-11
CA2339007A1 (en) 2000-02-17
NO20010553D0 (no) 2001-02-01
EA003205B1 (ru) 2003-02-27
NZ509561A (en) 2002-10-25
TR200100261T2 (tr) 2001-06-21
DE69908951D1 (de) 2003-07-24
BR9913357A (pt) 2001-05-15
IS5821A (is) 2001-01-23
PT1102747E (pt) 2003-09-30
FR2782082B3 (fr) 2000-09-22
DE69908951T2 (de) 2004-05-19
EP1102747A1 (de) 2001-05-30
DZ3074A1 (fr) 2004-07-20
HUP0103134A2 (en) 2002-06-29
EP1102747B1 (de) 2003-06-18
WO2000007987A1 (fr) 2000-02-17
JP2002522419A (ja) 2002-07-23
US7041679B2 (en) 2006-05-09
KR20010072220A (ko) 2001-07-31
AU748177B2 (en) 2002-05-30
PL345999A1 (en) 2002-01-14
CO5070576A1 (es) 2001-08-28
EE04274B1 (et) 2004-04-15
YU8601A (sh) 2003-07-07
US20040044215A1 (en) 2004-03-04
FR2782082A1 (fr) 2000-02-11
NO20010553L (no) 2001-04-05
AU5168599A (en) 2000-02-28
NO320645B1 (no) 2006-01-09
ATE243197T1 (de) 2003-07-15
AR019953A1 (es) 2002-03-27
CN1114592C (zh) 2003-07-16
HK1035535A1 (en) 2001-11-30

Similar Documents

Publication Publication Date Title
IL111960A (en) Morpholines and thiomorpholines their preparation and pharmaceutical compositions containing them
HUP9701281A2 (en) Piperidine derivatives as neurokinin antagonists and pharmaceutical compositions containing them
UA72890C2 (en) A crystalline form of osanetant (variants), a method for the preparation thereof (variants) and a pharmaceutical composition
NZ334017A (en) 1,4-di-substituted piperidines and use in combination with acetylcholinesterase inhibitors for treating cognitive disorders
AU5475896A (en) Dihydropyridine NPY antagonists: piperidine derivatives
MX9703025A (es) Proceso para preparar levobupivacaina y sus analogos.
HUP0900417A3 (en) Polymorphs of donepezil hydrochloride and process for production and pharmaceutical compositions containing them
SI1513528T1 (sl) Farmacevtski sestavek, ki vsebuje stabilizirano amorfno obliko donepezilijevega hidroklorida
HUT63384A (en) Process for producing new 1,2,3,6-tetrahydropyridine and piperidine derivatives substituted with n-(hydroxylalkyl) group and compositions comprising such compounds
SI2157083T1 (sl) Farmacevtske sestave, vsebujoče kristalno obliko (i) lerkanidipin hidroklorida
NO990721L (no) Stabil ikke-hygroskopisk krystallinsk form av N-[N-N-(4-(piperidin-4-yl)butanoyl)-N-etylglysyl]forbindelser
AU2455888A (en) 4-phenyl-4-(n-(phenyl)amido) piperidine derivatives and pharmaceutical compositions and method employing such compounds
NO20002450L (no) Sammenstilling av aktive bestanddeler, særlig tetrahydropyridiner og acetylcholinesterase-inhiberende midler, for behandling av senil demens av Alzheimer-type
MY118015A (en) Method of crystallizing a tetrahydropyridine derivative and crystalline forms thereby obtained
RU99115083A (ru) 1-фенилалкил-1,2,3,6-тетрагидропиридины для лечения болезни альцгеймера
HUP0105466A3 (en) Process for the preparation of a non-crystalline anhydrate form of paroxetine hydrochloride and pharmaceutical compositions containing them
NZ217818A (en) Substituted piperidine butanamide, n-oxides derivatives and pharmaceutical compositions
UA66776C2 (uk) Форма похідного тетрагідропіридину у вигляді мікрочастинок
BRPI0410934A (pt) método para a produção de chocolate, e, chocolate
HUP0302910A3 (en) Process for the racemisation of 1-benzyl-4-(4-fluorophenyl)-3-hydroxymethyl-1,2,3,6-tetrahydropyridine to be used as intermediate in the synthesis of paroxetine
CA2315696A1 (en) Pharmaceutical composition for oral administration
IL120870A0 (en) Carboxamide derivatives of pyrolidine piperidine and hexahydroazepine their preparation and pharmaceutical compositions containing them
HUP0002270A3 (en) Polymorphs of donepezil hydrochloride and process for production and pharmaceutical compositions containing them