AR015222A1 - Benzotiadiazoles, proceso para su preparacion, composicion farmaceutica que los contiene y su uso para la manufactura de un medicamento - Google Patents

Benzotiadiazoles, proceso para su preparacion, composicion farmaceutica que los contiene y su uso para la manufactura de un medicamento

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Publication number
AR015222A1
AR015222A1 ARP990100410A ARP990100410A AR015222A1 AR 015222 A1 AR015222 A1 AR 015222A1 AR P990100410 A ARP990100410 A AR P990100410A AR P990100410 A ARP990100410 A AR P990100410A AR 015222 A1 AR015222 A1 AR 015222A1
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AR
Argentina
Prior art keywords
alkyl
alk
manufacture
preparation
pharmaceutical composition
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ARP990100410A
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English (en)
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Novartis Ag
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Publication of AR015222A1 publication Critical patent/AR015222A1/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines 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 carbon atoms of the hetero ring
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    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/14Thiadiazoles; Hydrogenated thiadiazoles condensed with carbocyclic rings or ring systems
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Abstract

Benzotiadiazoles de la formula (I) en donde: -X- es O, S, N-CH3, -CH=CH- o -C(Alk)=C(Alk)-, en donde Alk es independientemente alquilo C1-4, R1 y R2 sonindependientemente hidrogeno, halogeno, alquilo C1-4, alcoxi C1-4, o trifluorometilo, y Het es unradical que tiene una de las formulas (a) a (p) en donde: R3y R8 son independientemente hidrogeno o alquilo C1-4; R4 es hidrogeno, alquilo C1-4, ciano, nitro, formilo o alquilo C1-4-carbonilo; R5 y R6 sonindependientemente hidrogeno, alquilo C1-7,al quenilo C3-7, cicloalquilo C3-7, cicloalquilo C3-7-alquilo C1-4, alcoxi C1-4-alquilo C2-5 o bencilo; R7 eshidrogeno, hidroxi, alquilo C1-4, o alcoxi C1-4; -W- es N, -C-CN, -C-NO2, -C-COH o -C-CO-Alk, en donde Alk es como se define anteriormente,y -X - es como sedefine anteriormente, en forma de base libre o de sal de adicion de ácido, un proceso para su preparacion, composicion farmacéutica que los contiene y su usopara la manufactura de un medicamento. Los compuestos de la formula (I) sonutile s como productos farmacéuticos que tienen actividad antagonista en losreceptores del factor de liberacion de la corticotropina.
ARP990100410A 1998-02-03 1999-02-01 Benzotiadiazoles, proceso para su preparacion, composicion farmaceutica que los contiene y su uso para la manufactura de un medicamento AR015222A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9802251.0A GB9802251D0 (en) 1998-02-03 1998-02-03 Organic compounds

Publications (1)

Publication Number Publication Date
AR015222A1 true AR015222A1 (es) 2001-04-18

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ARP990100410A AR015222A1 (es) 1998-02-03 1999-02-01 Benzotiadiazoles, proceso para su preparacion, composicion farmaceutica que los contiene y su uso para la manufactura de un medicamento

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EP (1) EP1049694B1 (es)
JP (1) JP3455180B2 (es)
KR (2) KR100507250B1 (es)
CN (1) CN1119346C (es)
AR (1) AR015222A1 (es)
AT (1) ATE217622T1 (es)
AU (1) AU745051B2 (es)
BR (1) BR9909739A (es)
CA (1) CA2318977A1 (es)
CO (1) CO4990932A1 (es)
DE (1) DE69901483T2 (es)
DK (1) DK1049694T3 (es)
ES (1) ES2178451T3 (es)
GB (1) GB9802251D0 (es)
HK (1) HK1033578A1 (es)
HU (1) HUP0100978A3 (es)
ID (1) ID26156A (es)
IL (1) IL137332A (es)
MY (1) MY122453A (es)
NO (1) NO316913B1 (es)
NZ (1) NZ505970A (es)
PE (1) PE20000246A1 (es)
PL (1) PL194838B1 (es)
PT (1) PT1049694E (es)
RU (1) RU2219177C2 (es)
SK (1) SK283833B6 (es)
TR (1) TR200002237T2 (es)
TW (1) TW509689B (es)
WO (1) WO1999040089A1 (es)
ZA (1) ZA99800B (es)

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PE20030008A1 (es) 2001-06-19 2003-01-22 Bristol Myers Squibb Co Inhibidores duales de pde 7 y pde 4
GB0302876D0 (en) * 2003-02-07 2003-03-12 Novartis Ag Organic compounds
EP2368554B1 (en) 2003-04-08 2014-12-24 Progenics Pharmaceuticals, Inc. Pharmaceutical formulations containing methylnaltrexone
AR057325A1 (es) 2005-05-25 2007-11-28 Progenics Pharm Inc Sintesis de (s)-n-metilnaltrexona, composiciones farmaceuticas y usos
AR057035A1 (es) 2005-05-25 2007-11-14 Progenics Pharm Inc SíNTESIS DE (R)-N-METILNALTREXONA, COMPOSICIONES FARMACÉUTICAS Y USOS
GB0525068D0 (en) 2005-12-08 2006-01-18 Novartis Ag Organic compounds
WO2007149938A2 (en) 2006-06-21 2007-12-27 The Salk Institute Biological Studies Methods for promoting hair growth
EP2137191B8 (en) 2007-03-29 2016-06-08 Progenics Pharmaceuticals, Inc. Peripheral opioid receptor antagonists and uses thereof
MX351611B (es) 2007-03-29 2017-10-20 Wyeth Llc Formas de cristal de bromuro de (r)-n-metilnaltrexona y uso de las mismas.
JP5469593B2 (ja) 2007-03-29 2014-04-16 ワイス・エルエルシー 末梢性オピオイド受容体アンタゴニストおよびその使用
EP2240489A1 (en) 2008-02-06 2010-10-20 Progenics Pharmaceuticals, Inc. Preparation and use of (r),(r)-2,2'-bis-methylnaltrexone
CA2676881C (en) 2008-09-30 2017-04-25 Wyeth Peripheral opioid receptor antagonists and uses thereof
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
WO2011092293A2 (en) 2010-02-01 2011-08-04 Novartis Ag Cyclohexyl amide derivatives as crf receptor antagonists
JP2013518085A (ja) 2010-02-01 2013-05-20 ノバルティス アーゲー CRF−1受容体アンタゴニストとしてのピラゾロ[5,1b]オキサゾール誘導体
WO2011095450A1 (en) 2010-02-02 2011-08-11 Novartis Ag Cyclohexyl amide derivatives as crf receptor antagonists
AR086554A1 (es) 2011-05-27 2014-01-08 Novartis Ag Derivados de la piperidina 3-espirociclica como agonistas de receptores de la ghrelina
KR20150003771A (ko) 2012-05-03 2015-01-09 노파르티스 아게 그렐린 수용체 효능제로서의 2,7-디아자-스피로[4.5]데스-7-일 유도체의 l-말레이트 염 및 그의 결정질 형태
WO2018048953A1 (en) * 2016-09-07 2018-03-15 The Regents Of The University Of California Allosteric corticotropin-releasing factor receptor 1 (crfr1) antagonists that decrease p-tau and improve cognition

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Publication number Priority date Publication date Assignee Title
FR2499991A1 (fr) * 1981-02-19 1982-08-20 Sandoz Sa Nouveaux 2,1,3-benzothiadiazoles et 2,1,3-benzoxadiazoles, leur preparation et leur application comme medicaments
EP0640595B1 (en) * 1992-04-28 1999-03-24 Yamanouchi Pharmaceutical Co. Ltd. Substituted tertiary amino compound or salt thereof
GB9323290D0 (en) * 1992-12-10 1994-01-05 Zeneca Ltd Quinazoline derivatives

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KR20010040550A (ko) 2001-05-15
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AU3252199A (en) 1999-08-23
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HUP0100978A2 (hu) 2002-05-29
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EP1049694A1 (en) 2000-11-08
ZA99800B (en) 1999-08-03
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