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34results about "Bisoxazines" patented technology

Methods of chemical synthesis and purification of diaminophenothiazinium compounds including methylthioninium chloride (MTC)

This invention pertains generally to the field of chemical synthesis and purification, and more specifically to methods of synthesizing and purifying certain 3,7 diamino-phenothiazin-5-ium compounds (referred to herein as “diaminophenothiazinium compounds”) including Methylthioninium Chloride (MTC) (also known as Methylene Blue). In one embodiment, the method comprises the steps of, in order: nitrosylation (NOS); nitrosyl reduction (NR); thiosulfonic acid formation (TSAF); oxidative coupling (OC); Cr(VI) reduction (CR); isolation and purification of zwitterionic intermediate (IAPOZI); ring closure (RC); chloride salt formation (CSF); one of: sulphide treatment (ST); dimethyldithiocarbamate treatment (DT); carbonate treatment (CT); ethylenediaminetetraacetic acid treatment (EDTAT); organic extraction (OE); and recrystallisation (RX). The present invention also pertains to the resulting (high purity) compounds, compositions comprising them (e.g., tablets, capsules), and their use in methods of inactivating pathogens, and methods of medical treatment and diagnosis, etc., for example, for tauopathies, Alzheimer's disease (AD), skin cancer, melanoma, viral diseases, bacterial diseases, or protozoal diseases. Wherein: each of R1 and R9 is independently selected from: —H; C1-4 alkenyl; and halogenated C1-4alkyl; each of R3NA and R3NB is independently selected from: C1-4 alkyl; C2-4alkenyl; and halogenated C4-1 alkyl; each of R7NA and R7NB is independently selected from: C1-4 alkyl; C2-4alkenyl; and halogenated C1-4 alkyl; and X is one or more anionic counter ions to achieve electrical neutrality.
Owner:WISTA LAB LTD

Methods of Chemical Synthesis and Purification of Diaminophenothiazinium Compounds Including Methylthioninium Chloride (Mtc)

This invention pertains generally to the field of chemical synthesis and purification, and more specifically to methods of synthesizing and purifying certain 3,7 diamino-phenothiazin-5-ium compounds (referred to herein as “diaminophenothiazinium compounds”) including Methylthioninium Chloride (MTC) (also known as Methylene Blue). In one embodiment, the method comprises the steps of, in order: nitrosylation (NOS); nitrosyl reduction (NR); thiosulfonic acid formation (TSAF); oxidative coupling (OC); Cr(VI) reduction (CR); isolation and purification of zwitterionic intermediate (IAPOZI); ring closure (RC); chloride salt formation (CSF); one of: sulphide treatment (ST); dimethyldithiocarbamate treatment (DT); carbonate treatment (CT); ethylenediaminetetraacetic acid treatment (EDTAT); organic extraction (OE); and recrystallisation (RX). The present invention also pertains to the resulting (high purity) compounds, compositions comprising them (e.g., tablets, capsules), and their use in methods of inactivating pathogens, and methods of medical treatment and diagnosis, etc., for example, for tauopathies, Alzheimer's disease (AD), skin cancer, melanoma, viral diseases, bacterial diseases, or protozoal diseases. Wherein: each of R1 and R9 is independently selected from: —H; C1-4 alkenyl; and halogenated C1-4alkyl; each of R3NA and R3NB is independently selected from: C1-4 alkyl; C2-4alkenyl; and halogenated C4-1 alkyl; each of R7NA and R7NB is independently selected from: C1-4 alkyl; C2-4alkenyl; and halogenated C1-4 alkyl; and X is one or more anionic counter ions to achieve electrical neutrality.
Owner:WISTA LAB LTD

Perpetration method for novel phenophosphazineanthracene dioxazine dye and application of novel phenophosphazineanthracene dioxazine dye to wool salt-free dyeing

The invention discloses a novel phenophosphazineanthracene dioxazine dye with a structural formula (I) as described in the specification, wherein R is H or HSO3, R1 is H, CH3 or C2H5, R2 is H, CH3 or C2H5, R3 is H, CH3 or C2H5, R5 is Cl, Br, or H, and R7 is Cl, Br or H. A preparation method for the novel phenophosphazineanthracene dioxazine dye comprises the following steps: a step I, by taking 5,10-dihydro-phenophosphazine-10-oxide and a derivative thereof as reactants, adding a nitryl reagent to react to obtain mononitride; a step II, performing hydrogenation reduction on a substance prepared in the step I; a step III, reacting an intermediate prepared in the step II in a non-proton solvent; a step IV, adding an oxidization ring-closing reagent into the dicondensate prepared in the step III in the non-proton solvent to obtain the dye. The dye has the characteristics of high coloring strength and color strength, and excellent heat resistance, permeation resistance, light resistance and weather resistance, can be used for dyeing wool, cotton fibers and nylons, has remarkable ultraviolet resistance and excellent water solubility, and can be used as ultraviolet-absorption-resistant dyes and ink-jet dyes.
Owner:崔金海
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