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RU93055131A - QUARTERLY AMIDES OF BASIC CHARACTER, METHOD OF THEIR PRODUCTION AND CONTAINING THEIR PHARMACEUTICAL COMPOSITION - Google Patents

QUARTERLY AMIDES OF BASIC CHARACTER, METHOD OF THEIR PRODUCTION AND CONTAINING THEIR PHARMACEUTICAL COMPOSITION

Info

Publication number
RU93055131A
RU93055131A RU93055131/04A RU93055131A RU93055131A RU 93055131 A RU93055131 A RU 93055131A RU 93055131/04 A RU93055131/04 A RU 93055131/04A RU 93055131 A RU93055131 A RU 93055131A RU 93055131 A RU93055131 A RU 93055131A
Authority
RU
Russia
Prior art keywords
group
denotes
production
amides
quarterly
Prior art date
Application number
RU93055131/04A
Other languages
Russian (ru)
Other versions
RU2120436C1 (en
Inventor
Эмон-Альт Ксавье
Гейль Патрик
Проиетто Винченцо
Ван Броек Дидиер
Original Assignee
Елф Санофи
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 FR9212083A external-priority patent/FR2696178B1/en
Application filed by Елф Санофи filed Critical Елф Санофи
Publication of RU93055131A publication Critical patent/RU93055131A/en
Application granted granted Critical
Publication of RU2120436C1 publication Critical patent/RU2120436C1/en

Links

Claims (1)

Изобретение относится к основным четвертичным амидам формулы:
Figure 00000001

в которой: Ar обозначает ароматическую или гетероароматическую, моно-, ди-, или трициклическую, в известных случаях замещенную, группу; Т обозначает прямую связь, гидроксиметилуновую группу, алкоксиметиленовую группу, алкоксильная группа которой содержит 1 - 4 С - атома; или С1 - С5 - алкиленовую группу; Ar′ обозначает незамещенный или одно- или многократно замещенный фенил, тиенил, бензотиенил, нафтил или индолил; R обозначает водород или C1 - C4 - алкил; Q обозначает водород; или Q и R вместе образуют 1,2-этиленовую, 1,3-пропиленовую или 1,4-бутиленовую группу; Ax обозначает радикал:
Figure 00000002

в которой X1, X2, X3 вместе и с атомом азота, с которым они связаны, образуют азабициклическую или азатрициклическую систему, в известных случаях замещенную фенильной группой; A обозначает фармацевтически приемлемый анион. Эти соединения пригодны для получения медикаментов, предназначенных для лечения патологий, связанных с системой тахикининов.
The invention relates to basic Quaternary amides of the formula:
Figure 00000001

in which: Ar denotes an aromatic or heteroaromatic, mono-, di-, or tricyclic, optionally substituted, group; T denotes a direct bond, a hydroxymethylune group, an alkoxymethylene group, the alkoxy group of which contains 1-4C-atoms; or C 1 - C 5 - alkylene group; Ar ′ is unsubstituted or mono- or multi-substituted phenyl, thienyl, benzothienyl, naphthyl, or indolyl; R denotes hydrogen or C 1 - C 4 - alkyl; Q is hydrogen; or Q and R together form a 1,2-ethylene, 1,3-propylene or 1,4-butylene group; A x denotes the radical:
Figure 00000002

in which X 1 , X 2 , X 3 together with the nitrogen atom to which they are bound, form an azabicyclic or azatricyclic system, in some cases substituted by a phenyl group; A denotes a pharmaceutically acceptable anion. These compounds are suitable for the production of drugs intended for the treatment of pathologies associated with the system of tachykinins.
RU93055131/04A 1992-09-30 1993-09-29 Basic type tertiary amides, methods of preparing thereof, and pharmaceutical composition comprising said compounds RU2120436C1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9212083A FR2696178B1 (en) 1992-09-30 1992-09-30 Quaternary basic amides, process for their preparation and pharmaceutical compositions containing them.
FR9212083 1992-09-30

Publications (2)

Publication Number Publication Date
RU93055131A true RU93055131A (en) 1996-04-27
RU2120436C1 RU2120436C1 (en) 1998-10-20

Family

ID=9434374

Family Applications (1)

Application Number Title Priority Date Filing Date
RU93055131/04A RU2120436C1 (en) 1992-09-30 1993-09-29 Basic type tertiary amides, methods of preparing thereof, and pharmaceutical composition comprising said compounds

Country Status (27)

Country Link
EP (1) EP0591040B1 (en)
JP (2) JP2857041B2 (en)
KR (1) KR100279084B1 (en)
CN (1) CN1036652C (en)
AT (1) ATE176469T1 (en)
AU (1) AU674875B2 (en)
BR (1) BR9303982A (en)
CA (1) CA2107432C (en)
CZ (1) CZ287272B6 (en)
DE (1) DE69323375T2 (en)
DK (1) DK0591040T3 (en)
ES (1) ES2130238T3 (en)
FI (1) FI114474B (en)
FR (1) FR2696178B1 (en)
GR (1) GR3030000T3 (en)
HU (2) HU215848B (en)
IL (1) IL107158A0 (en)
MX (1) MX9306024A (en)
MY (1) MY108881A (en)
NO (1) NO304888B1 (en)
NZ (1) NZ248821A (en)
OA (1) OA09869A (en)
RU (1) RU2120436C1 (en)
SG (1) SG47807A1 (en)
SI (1) SI9300513B (en)
TW (1) TW242625B (en)
ZA (1) ZA937276B (en)

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US5654316A (en) * 1995-06-06 1997-08-05 Schering Corporation Piperidine derivatives as neurokinin antagonists
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GB9712882D0 (en) * 1997-06-18 1997-08-20 Pfizer Ltd Quaternary ammonium compounds
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GB9716463D0 (en) * 1997-08-04 1997-10-08 Merck Sharp & Dohme Therapeutic agents
GB9716457D0 (en) * 1997-08-04 1997-10-08 Merck Sharp & Dohme Therapeutic agents
AU737019B2 (en) * 1997-08-04 2001-08-09 Merck Sharp & Dohme Limited Use of NK-1 receptor antagonists for treating aggressive behaviour disorders
GB9816897D0 (en) * 1998-08-04 1998-09-30 Merck Sharp & Dohme Therapeutic use
GB9927125D0 (en) 1999-11-16 2000-01-12 Univ Reading The Placental human neurokinin B precursor
EP1754701A4 (en) * 2004-02-25 2007-10-03 Sankyo Co Sulfonyloxy derivatives
JP2008534504A (en) 2005-03-22 2008-08-28 アゼヴァン ファーマスーティカルズ,インコーポレイテッド Β-Lactamyl alkanoic acid for treating premenstrual disorders
SI1910346T1 (en) 2005-07-19 2019-08-30 Azevan Pharmaceuticals, Inc. Beta-lactamyl phenylalanine, cysteine, and serine vasopressin antagonist
JP2010516731A (en) 2007-01-24 2010-05-20 グラクソ グループ リミテッド Pharmaceutical composition comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-1-yl) -benzyl]-(2S-phenyl-piperidin-3S-yl) -amine
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FI3122743T3 (en) 2014-03-28 2023-03-02 Azevan Pharmaceuticals Inc Compositions and methods for treating neurodegenerative diseases
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