35709-65-0Relevant academic research and scientific papers
Synthesis, analgesic, anti-inflammatory and anti-ulcerogenic activities of certain novel Schiff's bases as fenamate isosteres
Alafeefy, Ahmed M.,Bakht, Mohammed A.,Ganaie, Majid A.,Ansarie, Mohd N.,El-Sayed, Nahed N.,Awaad, Amani S.
, p. 179 - 183 (2015)
A series of certain novel Schiff bases as fenamate isosteres (VI:a-k) were synthesized to locate analgesic, anti-inflammatory agent with minimal ulcerogenic potential. The structures of the newly synthesized compounds were elucidated on the basis of their
Development of certain novel N-(2-(2-(2-oxoindolin-3-ylidene)hydrazinecarbonyl)phenyl)-benzamides and 3-(2-oxoindolin-3-ylideneamino)-2-substituted quinazolin-4(3 H)-ones as CFM-1 analogs: Design, synthesis, QSAR analysis and anticancer activity
Alafeefy, Ahmed M.,Ashour, Abdelkader E.,Prasad, Onkar,Sinha, Leena,Pathak, Shilendra,Alasmari, Fatimah A.,Rishi, Arun K.,Abdel-Aziz, Hatem A.
, p. 191 - 201 (2015/06/02)
The reaction of N-(2-(hydrazinecarbonyl)aryl)benzamides 2a, b with indoline-2,3-diones 4ae in acidified ethanolic solution furnished the corresponding N-(2-(2-(2-oxoindolin-3-ylidene)hydrazinecarbonyl)phenyl)benzamides 5aj, respectively. Furthermore, 3-(2
A New Synthesis of 2-Aryl-3,4-dihydro-5H-1,3,4-benzotriazepin-5-ones
Reddy, Ch. K.,Reddy, P. S. N.,Ratnam, C. V.
, p. 902 - 904 (2007/10/02)
The reaction of 2-aryl-3,1-benzoxazine-4-ones (1) and hydrazine hydrate in refluxing xylene yields 2-aryl-3,4-dihydro-5H-1,3,4-benzotriazepin-5-ones in 55-74percent yield.In basic conditions this reaction, however, gives 2-aryl-3-aminoquinazolin-4(3H)-one
