Patent classifications
C07C309/31
SALTS/COCRYSTALS OF (R)-N-(4-CHLOROPHENYL)-2-((1S,4S)-4-(6-FLUOROQUINOLIN-4-YL)CYCLOHEXYL)PROPANAMIDE
The present disclosure relates to amorphous and crystalline forms of (R)—N-(4-chlorophenyl)-2-((1S,4S)-4-(6-fluoro-quinolin-4-yl)cyclohexyl)propanamide and its salts/cocrystals, solvates, and/or hydrates, processes for their production, pharmaceutical compositions comprising them, and methods of treatment using them.
Amphiphilic Reaction Products from Vinylidene Olefins and Methods for Production Thereof
Compositions comprising one or more amphiphilic compounds formed from vinylidene olefins may comprise: a reaction product of one or more vinylidene olefins, in which the reaction product comprises a hydrophobic portion and a hydrophilic portion comprising a polar head group bonded to the hydrophobic portion. The one or more vinylidene olefins each comprise a vinylidene group that undergoes a reaction to become saturated and to produce at least part of the hydrophobic portion.
Amphiphilic Reaction Products from Vinylidene Olefins and Methods for Production Thereof
Compositions comprising one or more amphiphilic compounds formed from vinylidene olefins may comprise: a reaction product of one or more vinylidene olefins, in which the reaction product comprises a hydrophobic portion and a hydrophilic portion comprising a polar head group bonded to the hydrophobic portion. The one or more vinylidene olefins each comprise a vinylidene group that undergoes a reaction to become saturated and to produce at least part of the hydrophobic portion.
Amphiphilic Reaction Products from Vinylidene Olefins and Methods for Production Thereof
Compositions comprising one or more amphiphilic compounds formed from vinylidene olefins may comprise: a reaction product of one or more vinylidene olefins, in which the reaction product comprises a hydrophobic portion and a hydrophilic portion comprising a polar head group bonded to the hydrophobic portion. The one or more vinylidene olefins each comprise a vinylidene group that undergoes a reaction to become saturated and to produce at least part of the hydrophobic portion.
Bicyclic Surfactants
Fused and unfused bicyclic rings are a convenient scaffold for synthesizing various compounds. Amphiphilic compounds constructed upon a fused or unfused bicyclic ring scaffold may exhibit surfactant properties differing from those of more conventional classes of surfactants. Such amphiphilic compounds may have a structure of formula (I), wherein A is an aromatic ring, a heteroaromatic ring, or a cycloaliphatic ring, each ring being defined by 5 to 10 ring atoms, B is an aromatic ring or a heteroaromatic ring, each ring being defined by 5 to 6 ring atoms, wherein at least one G is a hydrophobic moiety and at least one G is a hydrophilic moiety, and z is 0 or a positive integer ranging up to the number of ring atoms in each of A and B; and wherein the hydrophobic moiety comprises branched or unbranched C.sub.6 to C.sub.30 alkyl or alkenyl group, and the hydrophilic moiety comprises a polar functional group selected from the group consisting of quaternary ammonium, sulfonate, sulfate, carboxylate, phosphate, and ethoxylated.
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Bicyclic Surfactants
Fused and unfused bicyclic rings are a convenient scaffold for synthesizing various compounds. Amphiphilic compounds constructed upon a fused or unfused bicyclic ring scaffold may exhibit surfactant properties differing from those of more conventional classes of surfactants. Such amphiphilic compounds may have a structure of formula (I), wherein A is an aromatic ring, a heteroaromatic ring, or a cycloaliphatic ring, each ring being defined by 5 to 10 ring atoms, B is an aromatic ring or a heteroaromatic ring, each ring being defined by 5 to 6 ring atoms, wherein at least one G is a hydrophobic moiety and at least one G is a hydrophilic moiety, and z is 0 or a positive integer ranging up to the number of ring atoms in each of A and B; and wherein the hydrophobic moiety comprises branched or unbranched C.sub.6 to C.sub.30 alkyl or alkenyl group, and the hydrophilic moiety comprises a polar functional group selected from the group consisting of quaternary ammonium, sulfonate, sulfate, carboxylate, phosphate, and ethoxylated.
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Polysulfonated fluorescence dyes
The invention relates to compounds of the general formulae (I)-(IV), which are characterized by substituents B comprising one or more sulfonic acid groups and their use as marker groups for the detection of analytes.
Polysulfonated fluorescence dyes
The invention relates to compounds of the general formulae (I)-(IV), which are characterized by substituents B comprising one or more sulfonic acid groups and their use as marker groups for the detection of analytes.
METHOD FOR PRODUCING SALT
According to the present invention, there is provided a method of producing a salt, including reacting M.sup.+X.sup.− with YH to generate XH and M.sup.+Y.sup.− and subsequently removing the generated XH to obtain the M.sup.+Y.sup.−.
In the method of producing a salt, M.sup.+X.sup.− is a salt of a cation represented by M.sup.+ and an anion represented by X.sup.−, M.sup.+Y.sup.− is a salt of the cation represented by M.sup.+ and an anion represented by Y.sup.−, XH is a conjugate acid of X.sup.−, YH is a conjugate acid of Y.sup.−, M.sup.+Y.sup.− is a compound that generates an acid upon irradiation with an active ray or a radioactive ray, a pKa of XH is larger than a pKa of YH, and a ClogP value of XH is larger than 2.
METHOD FOR PRODUCING SALT
According to the present invention, there is provided a method of producing a salt, including reacting M.sup.+X.sup.− with YH to generate XH and M.sup.+Y.sup.− and subsequently removing the generated XH to obtain the M.sup.+Y.sup.−.
In the method of producing a salt, M.sup.+X.sup.− is a salt of a cation represented by M.sup.+ and an anion represented by X.sup.−, M.sup.+Y.sup.− is a salt of the cation represented by M.sup.+ and an anion represented by Y.sup.−, XH is a conjugate acid of X.sup.−, YH is a conjugate acid of Y.sup.−, M.sup.+Y.sup.− is a compound that generates an acid upon irradiation with an active ray or a radioactive ray, a pKa of XH is larger than a pKa of YH, and a ClogP value of XH is larger than 2.