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RU93044129A - BRANCHED ALKYLAMINE DERIVATIVES OF THIAZOLE, METHOD FOR THEIR RECEIVING, USE AND CONTAINING THEIR PHARMACEUTICAL COMPOSITIONS - Google Patents

BRANCHED ALKYLAMINE DERIVATIVES OF THIAZOLE, METHOD FOR THEIR RECEIVING, USE AND CONTAINING THEIR PHARMACEUTICAL COMPOSITIONS

Info

Publication number
RU93044129A
RU93044129A RU93044129/04A RU93044129A RU93044129A RU 93044129 A RU93044129 A RU 93044129A RU 93044129/04 A RU93044129/04 A RU 93044129/04A RU 93044129 A RU93044129 A RU 93044129A RU 93044129 A RU93044129 A RU 93044129A
Authority
RU
Russia
Prior art keywords
radical
cycloalkyl
thiazole
receiving
alkyl
Prior art date
Application number
RU93044129/04A
Other languages
Russian (ru)
Other versions
RU2102389C1 (en
Inventor
Куртеманш Жий
Готье Клоди
Гюлли Даниель
Роже Пьер
Валетт Жерар
Жорж Вермют Камий
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 FR929207736A external-priority patent/FR2692893B1/en
Application filed by Елф Санофи filed Critical Елф Санофи
Publication of RU93044129A publication Critical patent/RU93044129A/en
Application granted granted Critical
Publication of RU2102389C1 publication Critical patent/RU2102389C1/en

Links

Claims (1)

Изобретение относится к производным формулы 1:
Figure 00000001

в которой R1 обозначает фенильный или нафтильный радикал (в известных случаях замещенные); R2 - атом водорода, галогена, алкильный радикал, оксиметильный или формильный радикал; R3 - алкильный радикал, циклоалкильный радикал, алкенильный радикал, циклоалкилалкильный радикал или фенильный радикал; R4 - атом водорода, алкильный, циклоалкильный или циклоалкилалкильный радикал; R5 - алкильный радикал, циклоалкильный радикал, циклоалкилалкильный радикал, алкенильный радикал или радикал формулы В:
Figure 00000002

R6 обозначает фенильный пиридильный, имидазолильный, пирролильный, тиенильный, фурильный радикал, в известных случаях замещенные, или циклоалкильный радикал.
The invention relates to derivatives of formula 1:
Figure 00000001

in which R 1 denotes a phenyl or naphthyl radical (in some cases substituted); R 2 is a hydrogen atom, halogen, alkyl radical, hydroxymethyl or formyl radical; R 3 is an alkyl radical, a cycloalkyl radical, an alkenyl radical, a cycloalkyl-alkyl radical or a phenyl radical; R 4 is a hydrogen atom, an alkyl, cycloalkyl or cycloalkylalkyl radical; R 5 is an alkyl radical, a cycloalkyl radical, a cycloalkyl-alkyl radical, an alkenyl radical or a radical of formula B:
Figure 00000002

R 6 denotes a phenyl pyridyl, imidazolyl, pyrrolyl, thienyl, furyl radical, in some cases substituted, or a cycloalkyl radical.
RU93044129A 1992-06-24 1993-06-23 Branched alkylamino derivatives of thiazole or their potential stereoisomers or their additive salts with mineral or organic acid, method for their production, pharmaceutical composition having activity in respect with factor of releasing of corticotropic hormone and alkylamino derivatives of thiazole as intermediate compounds RU2102389C1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9207736 1992-06-24
FR929207736A FR2692893B1 (en) 1992-06-24 1992-06-24 Branched alkylamino thiazole derivatives, processes for their preparation and pharmaceutical compositions containing them.

Publications (2)

Publication Number Publication Date
RU93044129A true RU93044129A (en) 1995-12-27
RU2102389C1 RU2102389C1 (en) 1998-01-20

Family

ID=9431129

Family Applications (1)

Application Number Title Priority Date Filing Date
RU93044129A RU2102389C1 (en) 1992-06-24 1993-06-23 Branched alkylamino derivatives of thiazole or their potential stereoisomers or their additive salts with mineral or organic acid, method for their production, pharmaceutical composition having activity in respect with factor of releasing of corticotropic hormone and alkylamino derivatives of thiazole as intermediate compounds

Country Status (30)

Country Link
US (1) US5464847A (en)
EP (1) EP0576350B1 (en)
JP (1) JPH0656809A (en)
KR (1) KR100228813B1 (en)
CN (1) CN1035552C (en)
AT (1) ATE159721T1 (en)
AU (1) AU665256B2 (en)
BR (1) BR9302643A (en)
CA (1) CA2099062A1 (en)
CZ (1) CZ125293A3 (en)
DE (1) DE69314855T2 (en)
DK (1) DK0576350T3 (en)
ES (1) ES2110070T3 (en)
FI (1) FI932909A (en)
FR (1) FR2692893B1 (en)
GR (1) GR3025684T3 (en)
HK (1) HK1002632A1 (en)
HU (1) HUT66384A (en)
IL (1) IL106088A (en)
IS (1) IS4040A (en)
MX (1) MX9303770A (en)
MY (1) MY109557A (en)
NO (1) NO303118B1 (en)
NZ (1) NZ247949A (en)
PH (1) PH30921A (en)
PL (2) PL176103B1 (en)
RU (1) RU2102389C1 (en)
SG (1) SG50626A1 (en)
SI (1) SI9300337A (en)
TW (1) TW256834B (en)

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US6432989B1 (en) 1999-08-27 2002-08-13 Pfizer Inc Use of CRF antagonists to treat circadian rhythm disorders
EP1149583A3 (en) * 2000-04-13 2001-11-14 Pfizer Products Inc. Combinations of corticotropin releasing factor antagonists and growth hormone secretagogues
US6699866B2 (en) * 2001-04-17 2004-03-02 Sepracor Inc. Thiazole and other heterocyclic ligands for mammalian dopamine, muscarinic and serotonin receptors and transporters, and methods of use thereof
WO2003006015A1 (en) * 2001-07-13 2003-01-23 Bristol-Myers Squibb Pharma Company Substituted thiazoles and oxazoles as corticotropin releasing hormone ligands
WO2003015777A1 (en) * 2001-08-13 2003-02-27 Lion Bioscience Ag Nr1h4 nuclear receptor binding compounds
ATE381542T1 (en) * 2001-08-13 2008-01-15 Phenex Pharmaceuticals Ag NR1H4 CORE RECEPTOR BINDING COMPOUNDS
JP4484439B2 (en) * 2002-03-14 2010-06-16 国立大学法人東京工業大学 VDAC regulator
WO2003075923A1 (en) * 2002-03-14 2003-09-18 Takeda Chemical Industries, Ltd. Vdac regulator
LT3002283T (en) * 2003-12-26 2017-09-11 Kyowa Hakko Kirin Co., Ltd. Thiazole derivatives
WO2007089679A2 (en) * 2006-02-01 2007-08-09 Merck & Co., Inc. Potassium channel inhibitors
AU2007312390B2 (en) * 2006-10-19 2013-03-28 F. Hoffmann-La Roche Ag Aminomethyl-4-imidazoles
JP5467735B2 (en) * 2007-07-02 2014-04-09 東ソー株式会社 Cylindrical sputtering target
US20170020877A1 (en) 2014-01-21 2017-01-26 Neurocrine Biosciences, Inc. Crf1 receptor antagonists for the treatment of congenital adrenal hyperplasia
JP2022500499A (en) 2018-09-07 2022-01-04 ピク セラピューティクス, インコーポレイテッド EIF4E Inhibitors and Their Use
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