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1. WO2002022592 - SUBSTITUTED UREA NEUROPEPTIDE Y Y5 RECEPTOR ANTAGONISTS

Publication Number WO/2002/022592
Publication Date 21.03.2002
International Application No. PCT/US2001/028324
International Filing Date 12.09.2001
Chapter 2 Demand Filed 15.03.2002
IPC
C07C 275/30 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
CACYCLIC OR CARBOCYCLIC COMPOUNDS
275Derivatives of urea, i.e. compounds containing any of the groups the nitrogen atoms not being part of nitro or nitroso groups
28having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
30being further substituted by halogen atoms, or by nitro or nitroso groups
C07C 311/07 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
CACYCLIC OR CARBOCYCLIC COMPOUNDS
311Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
02of an acyclic saturated carbon skeleton
07having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
C07D 211/58 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
211Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
04with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
06having no double bonds between ring members or between ring members and non-ring members
36with 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
56Nitrogen atoms
58attached in position 4
C07D 211/96 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
211Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
92with a hetero atom directly attached to the ring nitrogen atom
96Sulfur atom
C07D 401/04 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
401Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02containing two hetero rings
04directly linked by a ring-member-to-ring- member bond
C07D 401/06 2006.01
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
DHETEROCYCLIC COMPOUNDS
401Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02containing two hetero rings
06linked by a carbon chain containing only aliphatic carbon atoms
CPC
A61P 1/14
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
1Drugs for disorders of the alimentary tract or the digestive system
14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
A61P 1/16
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
1Drugs for disorders of the alimentary tract or the digestive system
16for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
A61P 11/00
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
11Drugs for disorders of the respiratory system
A61P 3/00
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
3Drugs for disorders of the metabolism
A61P 3/04
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
3Drugs for disorders of the metabolism
04Anorexiants; Antiobesity agents
A61P 3/06
AHUMAN NECESSITIES
61MEDICAL OR VETERINARY SCIENCE; HYGIENE
PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
3Drugs for disorders of the metabolism
06Antihyperlipidemics
Applicants
  • SCHERING CORPORATION [US]/[US]
Inventors
  • GREENLEE, William, J.
  • HUANG, Ying
  • KELLY, Joseph, M.
  • MC COMBIE, Stuart, W.
  • STAMFORD, Andrew, W.
  • WU, Yusheng
Agents
  • LEE, William, Y.
Priority Data
60/232,25514.09.2000US
Publication Language English (EN)
Filing Language English (EN)
Designated States
Title
(EN) SUBSTITUTED UREA NEUROPEPTIDE Y Y5 RECEPTOR ANTAGONISTS
(FR) ANTAGONISTES DU RECEPTEUR Y.Y5 DE NEUROPEPTIDE D'UREASE SUBSTITUE
Abstract
(EN)
Compounds represented by structural formula (I) including its N-oxides wherein Y is (a) or (b); R1 is H or (C1-C6)alkyl; R2 is H,(C1-C6)alkyl,(C3-C9)cycloalkyl or (C3-C7)cycloalkyl(C1-C6)alkyl; R3 is (c), (d), (e), (f), (g), (h) or (i); R4 is 1-3 substituents independently selected from the group consisting of H, -OH, halogen, haloalkyl,(C1-C6) alkyl, (C3-C7) cycloalkyl, (C3-C7) cycloalkyl (C1-C6) alkyl, -CN, -O(C1-C6) alkyl, -O(C3-C7) cycloalkyl, -O(C1-C6) alkyl (C3-C7) cycloalkyl, -S(C1-C6) alkyl, -S(C3-C7) cycloalkyl, -S(C1-C6) alkyl(C3-C7) cycloalkyl, -NH2, -NR9R10, -NO2, -CONH2, -CONR9R10 and NR2COR10; or where applicable, a geometric or optical isomer or a racemic mixture thereof, are claimed, as well as additional novel compounds; also claimed are pharmaceutical compositions and methods of using the aforesaid compounds in the treatment of obesity, eating disorders such as hyperphagia and diabetes.
(FR)
La présente invention concerne des composés représentés par la formule structurelle (I) comprenant ses oxyde de N. Dans cette formule Y est (I') R1 est H ou (C1-C6)alkyle; R2 est H, (C1-C6)alkyle, (C3-C9)cycloalkyle ou (C3-C7)cycloalkyle(C1-C6)alkyle; R3 est (II'); Z est OR10, -N(R9)(R10) ou - NH2; j est 0, 1 ou 2; k est 1 ou 2; l est 0, 1 ou 2; m est 0, 1 ou 2; R4 est 1- 3 substituants indépendamment sélectionné dans le groupe constitué de H, -OH, halogène, haloalkyle, (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, -CN, -O(C1-C6)alkyle, -O(C3-C7)cycloalkyle, -O(C1-C6)alkyle(C3-C7)cycloalkyle, -S(C1-C6)alkyle, -S(C3-C7)cycloalkyle, -S(C1-C6)alkyle(C3-C7)cycloalkyle, -NH2, -NR9R10, -NO2, -CONH2, -CONR9R10 et NR2COR10; R5 est 1-3 substituants indépendamment sélectionné dans le groupe constitué de H, halogène, -OH, haloalkyle, haloalcoxy, -CN, -NO2, (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, -O(C1-C6)alkyle, -O(C3-C7)cycloalkyle, -O(C1-C6)alkyleC3-C7)cycloalkyle, -CONH2 et -CONR9R10; R6 est -SO2(C1-C6)alkyle, -SO2(C3-C7)cycloalkyle, -SO2(C1-C6)alkyle(C3-C7)cycloalkyle, -SO2(C1-C6)haloalkyle, -SO2(hydroxy(C2-C6)alkyle), -SO2(amino(C2-C6)alkyle), -SO2(alcoxy(C2-C6)alkyle), -SO2(alkylamino(C2-C6)alkyle), -SO2(dialkylamino(C2-C6)alkyle), -SO2(aryle), -SO2(hétéroaryle), -SO2(aryle(C2-C6-alkyle), SO2NH2, -SO2NR9R10, -C(O)C1-C6alkyle, -C(O)C3-C7cycloalkyle, -C(O)aryle, - C(O)hétéroaryle, -C(O)NR9R10, -C(O)NH2, -C(S)NR9R10, -C(S)NH2, aryle, hétéroaryle, -(CH2)nC(O)NH2, -(CH2)nC(O)NR9R10,-C(=NCN)alkylthio, -C(=NCN)NR9R10, (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, aryle(C1-C6)alkyle, hétéroaryle(C1-C6)alkyle ou -C(O)OR9, n= 1 à 6; R7 = H ou alkyle; R8 est H, (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, aryle, hétéroaryle, -SO2(C1-C6)alkyle, -SO2(C3-C7)cycloalkyle, -SO2(C1-C6)alkyle(C3-C7)cycloalkyle, -SO2(C1-C6)haloalkyle ou -SO2(aryle); R9 est (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, aryle(C1-C6)alkyle, aryle ou hétéroaryle; et, R10 est hydrogène, (C1-C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)cycloalkyle(C1-C6)alkyle, aryle(C1-C6)alkyle, aryle ou hétéroaryle; ou une addition de sel et/ou d'hydrate de ces composés répondant aux normes pharmaceutiques, ou des promédicaments de ces composés, ou R9 et R10 pris ensemble peuvent former un cycle à 4-7 branches contenant 1 ou 2 hétéro-atomes. Cette invention concerne aussi un isomère géométrique ou optique ou un mélange racémique de ces composés, de même que de nouveau composés, des compositions parmaceutiques et des procédés d'utilisation des composés susmentionnés dans le traitement contre l'obésité, le traitement des troubles liés à l'alimentation tels que l'hyperphagie et le dabète.
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