Abstract:
Compounds of formula (II): wherein A, R 1 , R 2 , R 5 and R 13 are described herein, or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof, or a pharmaceutically acceptable salt or solvate thereof, are described herein, as well as other compounds. These compounds have activity as SHIP1 modulators, and thus may be useful in treating a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of the invention are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.
Abstract:
La présente invention concerne un procédé de fabrication de diaminomaléonitrile, caractérisé en ce qu'il comprend au moins une étape au cours de laquelle une cétone cyanhydrine de formule RR'COHCN, avec R et R' identique ou différent, représentant une chaîne aikyle linéaire ou ramifiée ayant de 1 à 5 carbones, réagit pour donner du diaminomaléonitrile.
Abstract:
Disclosed are compounds of formula (1) and (2) and/or E/E-, E/Z- or Z/Z geometrical isomer forms thereof; wherein R1-R5, R1-R11 and A are defined as in description. The compounds are used as UV absorbers for protecting household products from photolytic and oxidative degradation, as plastic additives, preferably for food and pharmaceutical packaging applications, for preventing photo-degradation of food by incorporation of the compounds of formula (1 ') and/or (2') into transparent food containers, for protection of UV-A sensitive drugs from photo-degradation by incorporation of UV absorber in transparent blister foils or transparent pharmacy containers, as additives for photographic and printing applications, as additives for electronic applications and protecting the ingredients in agriculture applications.
Abstract:
The present invention relates to methods for preparing substituted 3-cyanoquinolines and intermediates obtained by the methods of the present invention. The methods of the invention comprise reacting an N-aryl-2-propanimide with phosphoryl chloride to produce the substituted 3-cyanoquinolines. The methods further comprise reacting arylamines, orthoformates and active methylenes to produce the N-aryl-2-propenamide.
Abstract:
The present invention provides a process for the preparation of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-ethoxy-quinoline-3-carbonitrile comprising the steps and products disclosed within this application.
Abstract:
A compound of the Formula (I) wherein R 1 , R 2 , R 3 and R 4 are as defined herein. Further provided are methods of using such compounds for the treatment of diabetes and related diseases, and to pharmaceutical compositions containing such compounds.
Abstract:
4-haloalkyl nicotine nitriles (I) are suitable for use as intermediate products in the production of pesticides and can be obtained by means of a method which provides that a) 3-amino-1-haloalkyl-2-propen-1-one R-C(O)-CH=CH-NH2 (II) is reacted with a compound of formula (III) to (VII), (R Z)CH=CH-CN (III) (R Z)2CH-CH2-CN (IV) Hal-CH=CH-CN (V) Hal2CH-CH2CN (VI) HC=C-CN (VII) in a condensation reaction, R meaning (C1-C4)-haloalkyl R alkyl, Hal Cl or Br and Z meaning O, S, NR or OCO, and in the case of formula (IV), the two radicals Z being able to have the aforementioned meanings, independently of each other; to produce a compound of formula (VIII), (IX) and/or (X), R-C(O)-CH=CH-NH-CH=CH-CN (VIII) R-C(O)-CH=CH-NH-CH(ZR)-CH2-CN (IX) R-C(O)-CH=CH-NH-CH(Hal)-CH2-CN (X), R, Z and Hal having the meanings given above, and subjecting the product of the reaction b) to a ring closure reaction.
Abstract:
Substituted cyanoenamines of general formula (I) wherein Z, R , R and R are defined in the description, compositions thereof and methods for preparing the compounds are described. The compounds are useful in the treatment of diseases of the central nervous system, the cardiovascular system, the pulmonary system, the gastrointestinal system and the endocrinological system.
Abstract:
Disclosed are aminomethylenecyanoacetic acid esters and amides of formula (I), in which R?1 and R2¿, independently of each other, are phenyl, naphthyl, biphenyl or a five- or six-membered hetero-aryl group which has one, two or three nitrogen atoms or one oxygen atom or one sulphur atom or one nitrogen and one oxygen atom or one nitrogen and one sulphur atom, and which may be benzannulated, whereby these groups may be substituted by one to three C¿1?-C12-alkyl groups, C1-C12-alkoxy groups, halogen atoms, cyano groups, hydroxy groups or groups of the formulae COOR?3 COR3, CONHR3, OCOR3¿ or NHCOR3, where R3 is C1-C12-alkyl, C5-C8-cycloalkyl or phenyl; X is a C2-C30-alkylene group which may contain non-adjacent oxygen atoms, a C4-C12-alkylene or C4-C12-alkinylene group (the unsaturated bonds not being adjacent to the ester oxygen atoms), a C5-C8-cycloalkylene group or a phenylene group; and Y is O or NH. These compounds can be used as stabilizers for organic materials.