2567-62-6

Upstream product

• 490-56-2 3-phenyl-oxazolidine-2,5-dione 
• 62-53-3 aniline 
• 64-17-5 ethanol 
• 14181-81-8 2-anilino-N,N'-diphenyl-acetamidine 
• 142-04-1 aniline hydrochloride 
• 51118-10-6 2-anilino-1-phenyl-ethanone (Z)-oxime 
• 105-39-5 chloroacetic acid ethyl ester 
• 587-65-5 N-chloroacetyl-aniline 
• 79-11-8 chloroacetic acid 
• 79-04-9 chloroacetyl chloride 
• 4727-41-7 dimethylsulfonioacetate 
• 5326-87-4 N-(phenyl)bromoacetamide 
• 79-07-2 Chloroacetamide 
• 10258-71-6 α-azidoacetanilide 

Downstream Products

• 3157-03-7 1,3-diphenyl imidazolidine-2,4-dione 
• 621-09-0 N,N'-diphenylacetamidine 
• 71607-45-9 N,N-Diphenyl-acetamidine 
• 855931-91-8 N-nitroso-N-phenyl-glycine anilide 
• 103-01-5 N-Phenylglycine 
• 482-89-3 1H,1H'-2,2'-Biindolylidene-3,3'-dione 
• 20635-51-2 1,4-diphenylpiperazine-2,5-dione 
• 743422-98-2 N-phenyl-N-(phenylcarbamoyl-methyl)-glycine 
• 74339-86-9 N-chloroacetyl-N-phenyl-glycine anilide 
• 14181-81-8 2-anilino-N,N'-diphenyl-acetamidine 
• 30810-75-4 1,4-diphenyl-piperazine-2,6-dione 
• 107306-22-9 N¹,N²-diphenyl-N-phenyl-N-benzoylglycineamidine 
• 873978-25-7 (N-phenyl-hydrazino)-acetic acid anilide 

Relevant academic research and scientific papers

Visible-Light-Driven Aryl Migration and Cyclization of α-Azido Amides

This paper reports two new visible-light-promoted radical reactions of α-azido amides. By catalysis of [Ir(ppy)2(dtbbpy)]PF6 with i-Pr2NEt as the reducing agent, N-aryl α-azido tertiary amides were first converted to the corresponding aminyl radicals through reduction of the azido group; the aminyl radicals then underwent N-to-N aryl migration to give α-anilinyl-functionalized amides. α-Azido secondary amides, on the other hand, reacted with the solvent ethanol and i-Pr2NEt to afford the imidazolinone products.

Ru(II)-Pheox catalyzed N-H insertion reaction of diazoacetamides: Synthesis of N-substituted α-aminoamides

An efficient protocol for the preparation of α-aminoamides was developed via the Ru(II)-dm-Pheox catalyzed N-H insertion reaction of various diazoacetamides with several amines, including aniline. This catalytic N-H insertion reaction was also applied to the synthesis of 2-(2-methylquinolin-4- ylamino)-N-phenylacetamide, a potential antileishmanial agent.

Synthesis of α-amino acid amides: Ruthenium-catalyzed amination of α-hydroxy amides

Give me an N: The catalytic amination of α-hydroxy amides with a variety of amines, including anilines, primary and secondary aliphatic amines, and ammonia, yields a wide range of α-amino amides (see scheme). This atom-efficient amination protocol proceeds efficiently in the presence of a commercially available [Ru3(CO)12]/DCPE catalyst system. Copyright

Synthesis of a novel quinoline derivative, 2-(2-methylquinolin-4-ylamino)-N-phenylacetamide - A potential antileishmanial agent

Some novel quinoline derivatives were prepared and tested for antileishmanial activity. 2-(2-Methylquinolin-4-ylamino)-N-phenylacetamide (2) was found to be significantly more active than the standard antileishmanial drug sodium antimony gluconate (SAG) i

Reaction of Azides in Presence of Aluminium Chloride

Amidoalkylazides (2) on treatment with aluminium chloride in benzene yield 2-anilino-N-(aryl)acetamides (3) in good yields.