C07D207/267

Alpha-cinnamide compounds and compositions as HDAC8 inhibitors

The present invention relates to inhibitors of histone deacetylases, in particular HDAC8, that are useful for the treatment of cancer and other diseases and disorders, as well as the synthesis and applications of said inhibitors.

Alpha-cinnamide compounds and compositions as HDAC8 inhibitors

The present invention relates to inhibitors of histone deacetylases, in particular HDAC8, that are useful for the treatment of cancer and other diseases and disorders, as well as the synthesis and applications of said inhibitors.

N-methyl-2-pyrrolidone distilling apparatus

A distillation apparatus for NMP including a first distillation column in which the spent NMP as a liquid to be treated is subjected to distillation; and a second distillation column in which bottoms from the first distillation column are further subjected to distillation, the distillation apparatus being provided with an automatic treatment function including a start-up function, and then a continuous treatment operation of the distillation apparatus being initiated; and an operational mode switching function in which upon the continuous treatment operation, an operational mode of the distillation apparatus being switched again to the circulation operation according to a level of the liquid in the raw material tank or a level of the liquid in the product tank.

N-methyl-2-pyrrolidone distilling apparatus

A distillation apparatus for NMP including a first distillation column in which the spent NMP as a liquid to be treated is subjected to distillation; and a second distillation column in which bottoms from the first distillation column are further subjected to distillation, the distillation apparatus being provided with an automatic treatment function including a start-up function, and then a continuous treatment operation of the distillation apparatus being initiated; and an operational mode switching function in which upon the continuous treatment operation, an operational mode of the distillation apparatus being switched again to the circulation operation according to a level of the liquid in the raw material tank or a level of the liquid in the product tank.

2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine analogs and methods for their synthesis and use

The present invention relates to novel 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine analogs, and methods for their synthesis and use. Such analogs are designed to provide a convenient linkage chemistry for coupling under mild conditions to a suitable group on a target protein, polypeptide, solid phase or detectable label.

2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine analogs and methods for their synthesis and use

The present invention relates to novel 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine analogs, and methods for their synthesis and use. Such analogs are designed to provide a convenient linkage chemistry for coupling under mild conditions to a suitable group on a target protein, polypeptide, solid phase or detectable label.

METHOD FOR SYNTHESIZING LACTAM DERIVATIVES WITHOUT USE OF CATALYST
20220177429 · 2022-06-09 · ·

Disclosed is a simple synthesis method of lactam derivatives, comprising: with formamide functioning as both an amine source and a hydrogen source (hydrolyzed to produce formic acid), carrying out a cycloamination reaction on a raw material keto acid in the absence of a solvent or a catalyst to simply synthesize a lactam derivative. Compared with previous reports, the present disclosure has the following advantages: the time required for the reaction is greatly shortened, the selectivity is remarkably improved, a conversion rate of a keto acid derivative is greater than 99%, and the yield of the lactam derivative can reach 70% to 94%.

METHOD FOR SYNTHESIZING LACTAM DERIVATIVES WITHOUT USE OF CATALYST
20220177429 · 2022-06-09 · ·

Disclosed is a simple synthesis method of lactam derivatives, comprising: with formamide functioning as both an amine source and a hydrogen source (hydrolyzed to produce formic acid), carrying out a cycloamination reaction on a raw material keto acid in the absence of a solvent or a catalyst to simply synthesize a lactam derivative. Compared with previous reports, the present disclosure has the following advantages: the time required for the reaction is greatly shortened, the selectivity is remarkably improved, a conversion rate of a keto acid derivative is greater than 99%, and the yield of the lactam derivative can reach 70% to 94%.

Metal complex, method for producing same, and method for producing gamma-lactam compound using same

The present invention relates to a novel metal complex, a method for producing same, and a method for producing a gamma-lactam compound using same, and the metal complex according to the present invention is used as a catalyst for producing a gamma-lactam compound and can efficiently produce a gamma-lactam compound with an excellent yield and excellent selectivity.

Metal complex, method for producing same, and method for producing gamma-lactam compound using same

The present invention relates to a novel metal complex, a method for producing same, and a method for producing a gamma-lactam compound using same, and the metal complex according to the present invention is used as a catalyst for producing a gamma-lactam compound and can efficiently produce a gamma-lactam compound with an excellent yield and excellent selectivity.