6004-21-3

Usage

InChI:InChI=1/C13H10ClNO/c14-11-7-4-8-12(9-11)15-13(16)10-5-2-1-3-6-10/h1-9H,(H,15,16)

Upstream product

• 98-88-4 benzoyl chloride 
• 108-42-9 3-chloro-aniline 
• 93-59-4 Perbenzoic acid 
• 3460-08-0 N¹-benzoyl-N¹,N²-diphenylacetamidine 
• 100-09-4 4-methoxybenzoic acid 
• 93-97-0 benzoic acid anhydride 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 
• 100-51-6 benzyl alcohol 
• 108-37-2 1-bromo-3-chlorobenzene 
• 55-21-0 benzamide 
• 65-85-0 benzoic acid 
• 625-99-0 3-iodochlorobenzene 
• 932-90-1 Benzaldoxime 

Downstream Products

• 34918-77-9 N-(3-chlorophenyl)benzimidoyl chloride 
• 10286-75-6 N-(3,4-dichlorophenyl)benzamide 
• 5969-74-4 Benzoyl-(3-chloro-phenyl)-carbamic acid 1-methyl-butyl ester 
• 6167-08-4 Benzoyl-(3-chloro-phenyl)-carbamic acid 1-methyl-pentyl ester 
• 6064-03-5 Benzoyl-(3-chloro-phenyl)-carbamic acid 2-methoxy-1-methyl-ethyl ester 
• 10278-49-6 N-(3-chlorophenyl) benzothioamide 
• 1019-90-5 5-chloro-2-phenyl-1,3-benzoxazole 
• 952-16-9 5-chloro-2-phenylbenzothiazole 
• 108-42-9 3-chloro-aniline 
• 100-51-6 benzyl alcohol 
• 57039-63-1 6-chloro-2-phenylindole 
• 93-98-1 N-phenyl benzoyl amide 
• 5866-89-7 Benzoyl-(3-chloro-phenyl)-carbamic acid isopropyl ester 
• 50798-95-3 N-benzyl-3-chloroaniline 

Relevant academic research and scientific papers

Single-pot tandem oxidative/C-H modification amidation process using ultrasmall PdNP-encapsulated porous organosilica nanotubes

Herein, we studied a single-pot method with a dual catalysis process towards the conversion of primary aromatic alcohols to amides using ultrasmall PdNPs of controlled uniform size (1.8 nm) inside hybrid mesoporous organosilica nanotubes (MO-NTs). The cat

Room-temperature copper-catalyzed electrophilic amination of arylcadmium iodides with ketoximes

We started our study by preparation two ketoximes. Later, there were studies to reveal these ketoximes' effects in the electrophilic amination reaction with organocadmium reagents. Primarily, it was observed that arylcadmium iodides could not be reacted with ketoximes at room temperature in the absence of a catalyst. CuCN was a suitable catalyst for this electrophilic amination reaction of arylcadmium iodides and allowed the preparation of functionalized aniline derivatives in good yields under mild reaction conditions. We obtained the results indicated that the yield of primary arylamines was strongly dependent on the steric and electronic effects of organocadmium reagent and amination agent. In the case of both amination reagents, meta-substituted arylamines were obtained in higher yields than para-substituted arylamines. We observed that acetone O-(4-chlorophenylsulfonyl)oxime, 1, as an aminating agent, was more successful than acetone O-(2-Naphthylsulfonyl)oxime, 2, in the synthesis of functionalized arylamines by electrophilic amination of corresponding aryl cadmium iodides. In this method, there is no cadmium release to the environment.

COLORANT DISPERSION LIQUID AND PRINTING METHOD OF HYDROPHOBIC FIBER

PROBLEM TO BE SOLVED: To provide black dispersion liquid for inkjet printing ink that can manufacture a dyed thing excellent in color rendering, can obtain high quality dyed thing that can obtain high concentration dyed thing, and has excellent redispersion. SOLUTION: A colorant dispersion comprises (A) a compound expressed by a formula (1), and (B) polyoxyethylene arylphenyl ether-based dispersant and polyoxyethylene arylphenyl ether sulfate-based dispersant. (R1 is H or a nitro group; R2 and R3 are independently C1 to C4 alkoxy group or C1 to C4 alkyl group that may be substituted with a phenyl group; R4 is halogen atom; and R2 and R3 may be mutually coupled to form a ring.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

High yielding electrophilic amination with lower order and?higher order organocuprates: Application of acetone O-(4-Chlorophenylsulfonyl)oxime in the construction of the C?N bond at room temperature

Electrophilic amination reaction was performed with lower order and?higher order organocuprates using acetone O-(4-Chlorophenylsulfonyl)oxime (1). It was proceeded smoothly at room temperature in the presence of organocuprates to provide the corresponding primary amines in good yields with 10 and 60 min, respectively. The primary amine yields of the electrophilic amination of bromomagnesium organocyanocuprates and dibromomagnesium diorganocyanocuprates were obtained 52–72% and 58–83%, respectively. We observed that higher order organocuprates were more successful than lower order organocuprates in the synthesis of functionalized arylamines by electrophilic amination.

COLORED DISPERSION, INK COMPOSITION USING THE SAME, AND DISPERSION STABILITY IMPROVEMENT METHOD THEREWITH AND PRINTING METHOD OF HYDROPHOBIC FIBER

PROBLEM TO BE SOLVED: To provide dispersion liquid for inkjet printing ink that can manufacture a dyed thing excellent in color rendering, can obtain the dyeing having high sublimation transfer efficiency, high concentration and high quality, in sublimation transfer dying using inkjet printing, furthermore, excellent in storage stability. SOLUTION: A colorant dispersion comprises (A) a compound expressed by a formula (1), (B) C.I. Disperse Blue 360, and (C) a dispersant, in which when a total content of (A) and (B) is set to 100, a content of (B) is 10 or larger and 90 or smaller, (C) the dispersant contains at least any one selected from the group consisting of polyoxyethylene aryl phenyl ether-based dispersant, and polyoxyethylene arylphenyl ether sulfate-based dispersant. (R1 is H or a nitro group; R2 and R3 may be independently substituted with C1-C4 alkoxy group or C1-C4 alkyl groups that may be substituted with phenyl group; R4 is halogen atom; and R2 and R3 may be mutually coupling to form a ring.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Regioselective Synthesis of 2° Amides Using Visible-Light-Induced Photoredox-Catalyzed Nonaqueous Oxidative C-N Cleavage of N, N-Dibenzylanilines

A visible-light-driven photoredox-catalyzed nonaqueous oxidative C-N cleavage of N,N-dibenzylanilines to 2° amides is reported. Further, we have applied this protocol on 2-(dibenzylamino)benzamide to afford quinazolinones with (NH4)2S2O8 as an additive. Mechanistic studies imply that the reaction might undergo in situ generation of α-amino radical to imine by C-N bond cleavage followed by the addition of superoxide ion to form amides.

Chromium-catalyzed ligand-free amidation of esters with anilines

Amides are important structural motifs in pharmaceutical and agrochemical chemistry because of the intriguing biological active properties. We report here the amidation of commercially available esters with anilines that was promoted by low-cost and air-stable chromium(III) pre-catalyst combined with magnesium, providing access to amides. This reaction occurs without the use of external ligands in a simple operation. Mechanistic studies indicate that a reactive aminated Cr species responsible for the amidation can be considered, which may be formed by reaction of low-valent Cr with aniline followed by reduction with hydrogen evolution.

Copper-catalyzed aerobic oxidative C-C bond cleavage of simple ketones for the synthesis of amides

A Cu-catalyzed oxidative amidation of simple ketones with amines via carbon-carbon (C-C) bond cleavage has been developed. A number of aryl and alkyl ketones could be easily converted to amides using cheap copper salt as the catalyst and O2 as the oxidant with a wide range of amines, including primary and secondary amines. This method shows a notable advantage of the broad scope for the substrate, thus providing a practical approach to amides. A plausible mechanism is proposed based on the preliminary experiments.

Switching from biaryl formation to amidation with convoluted polymeric nickel catalysis

A stable, reusable, and insoluble poly(4-vinyl-pyridine) nickel catalyst (P4VP-NiCl2) was prepared through the molecular convolution of poly(4-vinylpyridine) (P4VP) and nickel chloride. We proposed a coordination structure of the Ni center in the precatalyst based on elemental analysis and Ni K-edge XANES, and we confirmed that it is consistent with Ni K-edge EXAFS. The Suzuki?Miyaura-type coupling of aryl halides and arylboronic esters proceeded using P4VP-NiCl2 (0.1 mol % Ni) to give the corresponding biaryl compounds in up to 94% yield. Surprisingly, when the same reaction of aryl halides and arylboronic acid/ester was carried out in the presence of amides, the amidation proceeded predominantly to give the corresponding arylamides in up to 99% yield. In contrast, the reaction of aryl halides and amides in the absence of arylboronic acid/ester did not proceed. P4VP-NiCl2 successfully catalyzed the lactamization for preparing phenanthridinone. P4VP-NiCl2 was reused five times without significant loss of catalytic activity. Pharmaceuticals, natural products, and biologically active compounds were synthesized efficiently using P4VPNiCl2 catalysis. Nickel contamination in the prepared pharmaceutical compounds was not detected by ICP-MS analysis. The reaction was scaled to multigrams without any loss of chemical yield. Mechanistic studies for both Suzuki?Miyaura and amidation were performed.

COMPOUNDS AND METHODS OF INHIBITING BACTERIAL CHAPERONIN SYSTEMS

The present disclosure relates to novel compounds and methods of killing or inhibiting the growth of bacteria. In some embodiments, a method of killing or inhibiting the growth of bacteria is provided. The method comprises administering a compound of formula I or a pharmaceutically acceptable salt thereof to bacteria. In some embodiments, a method of killing or inhibiting the growth of bacteria is provided. The method comprises administering an anthelmintic to bacteria.