Patent classifications
C07C381/00
Method for producing nitrogen-containing pentafluorosulfanylbenzene compound
A method for producing a nitrogen-containing pentafluorosulfanylbenzene compound of formula (2a) or (2b): ##STR00001## (wherein R.sup.1 a hydrogen atom or a hydrocarbon group; Z is an aryl group linked to a carbonyl group; Y is a group of formula (Y1), (Y2), (Y3), or (Y4); R.sub.2 is a hydrogen atom or a hydrocarbon group) ##STR00002## the method comprising reacting a halogeno-pentafluorosulfanylbenzene compound of formula (1) with a nitrogenous nucleophile: ##STR00003## (wherein X is a halogen atom; n is an integer of 1 to 5; R.sup.1 is as defined above).
Method for producing nitrogen-containing pentafluorosulfanylbenzene compound
A method for producing a nitrogen-containing pentafluorosulfanylbenzene compound of formula (2a) or (2b): ##STR00001## (wherein R.sup.1 a hydrogen atom or a hydrocarbon group; Z is an aryl group linked to a carbonyl group; Y is a group of formula (Y1), (Y2), (Y3), or (Y4); R.sub.2 is a hydrogen atom or a hydrocarbon group) ##STR00002## the method comprising reacting a halogeno-pentafluorosulfanylbenzene compound of formula (1) with a nitrogenous nucleophile: ##STR00003## (wherein X is a halogen atom; n is an integer of 1 to 5; R.sup.1 is as defined above).
SULFINYLAMINOBENZAMIDE AND SULFONYLAMINOBENZAMIDE DERIVATIVES
Provided is a compound of Formula (I):
##STR00001## wherein the variable groups are defined herein.
Liquid crystal compound, liquid crystal composition and liquid crystal display device
A solution is a compound represented by formula (1), a liquid crystal composition containing the compound and a liquid crystal display device including the composition. ##STR00001## In formula (1), R.sup.a and R.sup.b are independently alkyl having 1 to 30 carbons or the like; and X and Y are independently fluoroalkyl having 1 to 5 carbons, fluoroalkoxy having 1 to 5 carbons or pentafluorosulfanil, and one of X and Y may be fluorine.
Liquid crystal compound, liquid crystal composition and liquid crystal display device
A solution is a compound represented by formula (1), a liquid crystal composition containing the compound and a liquid crystal display device including the composition. ##STR00001## In formula (1), R.sup.a and R.sup.b are independently alkyl having 1 to 30 carbons or the like; and X and Y are independently fluoroalkyl having 1 to 5 carbons, fluoroalkoxy having 1 to 5 carbons or pentafluorosulfanil, and one of X and Y may be fluorine.
Aryloyl(oxy or amino)pentafluorosulfanylbenzene compound, pharmaceutically acceptable salt thereof, and prodrugs thereof
An aryloyl(oxy or amino)pentafluorosulfanylbenzene compound having pharmacological action. The aryloyl(oxy or amino)pentafluorosulfanylbenzene compound is represented by general formula (A-I), a pharmaceutically acceptable salt thereof, and a prodrug thereof, ##STR00001##
wherein all of parameters represent the same meanings as defined in the specification.
Aryloyl(oxy or amino)pentafluorosulfanylbenzene compound, pharmaceutically acceptable salt thereof, and prodrugs thereof
An aryloyl(oxy or amino)pentafluorosulfanylbenzene compound having pharmacological action. The aryloyl(oxy or amino)pentafluorosulfanylbenzene compound is represented by general formula (A-I), a pharmaceutically acceptable salt thereof, and a prodrug thereof, ##STR00001##
wherein all of parameters represent the same meanings as defined in the specification.
Industrial methods for producing arylsulfur pentafluorides
Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.
Industrial methods for producing arylsulfur pentafluorides
Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.
Integrin antagonist conjugates for targeted delivery to cells expressing LFA-1
The invention relates to compounds of formula (I), wherein R1, R2, and n are defined in the detailed description and claims. In particular, the present invention relates to the compounds of formula I for use in the manufacture and delivery of conjugated moieties such as small molecules, peptides, nucleic acids, fluorescent moieties, and polymers which are linked to LFA-1 integrin antagonists to target cells expressing LFA-1. ##STR00001##