C07C251/16

Racemic beta-aminosulfone compounds

It is described an industrially viable and advantageous process for the preparation of racemic beta-aminosulfone (1), an useful intermediate for the preparation of N-(2-((1S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl)acetamide, also known as Apremilast, the latter being suitable for use in methods of treating, preventing and/or managing psoriasis or psoriatic arthritis.

Acetophenone compound, preparation method thereof, and application thereof in fatty liver prevention and treatment

Disclosed is a compound represented by formula I or a pharmaceutically acceptable salt thereof, preparation method thereof, and use thereof in preventing or treating fatty liver or in preparing pharmaceuticals for weight loss. ##STR00001##

Acetophenone compound, preparation method thereof, and application thereof in fatty liver prevention and treatment

Disclosed is a compound represented by formula I or a pharmaceutically acceptable salt thereof, preparation method thereof, and use thereof in preventing or treating fatty liver or in preparing pharmaceuticals for weight loss. ##STR00001##

RACEMIC BETA-AMINOSULFONE COMPOUNDS

It is described an industrially viable and advantageous process for the preparation of racemic beta-aminosulfone (1), an useful intermediate for the preparation of N-(2-((1S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl)acetamide, also known as Apremilast, the latter being suitable for use in methods of treating, preventing and/or managing psoriasis or psoriatic arthritis.

##STR00001##

CINCHONINE-DERIVED CATALYSTS AND METHODS OF USING SAME
20200048243 · 2020-02-13 · ·

The present invention includes certain conchinine-derived phase-transfer catalysts of formula (I), compositions comprising the same, and methods of promoting asymmetric addition reactions using the same.

##STR00001##

CINCHONINE-DERIVED CATALYSTS AND METHODS OF USING SAME
20200048243 · 2020-02-13 · ·

The present invention includes certain conchinine-derived phase-transfer catalysts of formula (I), compositions comprising the same, and methods of promoting asymmetric addition reactions using the same.

##STR00001##

Acetophenone Compound, Preparation Method Thereof, And Application Thereof In Fatty Liver Prevention And Treatment

Disclosed is a compound represented by formula I or a pharmaceutically acceptable salt thereof, preparation method thereof, and use thereof in preventing or treating fatty liver or in preparing pharmaceuticals for weight loss.

##STR00001##

SYNTHESES OF N-HETEROCYCLIC CARBENES AND INTERMEDIATES THEREFOR
20180186754 · 2018-07-05 ·

A method of preparing a 2,6 disubstituted anilines includes, reacting a 2-amino isophthalic acid diester with sufficient Grignard reagent R.sub.2CH.sub.2MgX to form the corresponding diol product, dehydrating the diol product to the corresponding dialkene; and hydrogenating the diol product to form the corresponding aniline. The 2,6 disubstituted anilines can be used to produce N-Heterocyclic Carbenes (NHCs). The NHCs can find application in various fields such as organic synthesis, catalysis and macromolecular chemistry. Palladium catalysts containing the NHCs are also described.

SYNTHESES OF N-HETEROCYCLIC CARBENES AND INTERMEDIATES THEREFOR
20180186754 · 2018-07-05 ·

A method of preparing a 2,6 disubstituted anilines includes, reacting a 2-amino isophthalic acid diester with sufficient Grignard reagent R.sub.2CH.sub.2MgX to form the corresponding diol product, dehydrating the diol product to the corresponding dialkene; and hydrogenating the diol product to form the corresponding aniline. The 2,6 disubstituted anilines can be used to produce N-Heterocyclic Carbenes (NHCs). The NHCs can find application in various fields such as organic synthesis, catalysis and macromolecular chemistry. Palladium catalysts containing the NHCs are also described.

Ketene imine compound, polyester film, back sheet for solar cell module, and solar cell module

A polyester resin composition including a ketene imine compound represented by the Formula (1) and polyester shows excellent hydrolysis resistance and prevents yellowing. At least one of R.sub.11, R.sub.12, R.sub.21 and R.sub.22 represents an alkyl, aryl, alkoxy or aryloxy group which may have a substituent; R.sub.15 and R.sub.25 represent an alkyl, aryl, alkoxy or aryloxy group which may have a substituent; R.sub.3 represents an alkyl or aryl group which may have a substituent; and a and b represent an integer of 0 to 3. ##STR00001##