6320-47-4

Usage

InChI:InChI=1/C11H10N2O/c1-8-7-10(13-11(14)12-8)9-5-3-2-4-6-9/h2-7H,1H3,(H,12,13,14)

Upstream product

• 77517-13-6 (4-Phenyl-6-methyl-2-pyrimidinylthio)acetic Acid 
• 57-13-6 urea 
• 93-91-4 1-phenylbutan-1,3-dione 
• 495-41-0 1-phenylbut-2-en-1-one 
• 58006-77-2 4,7-dihydro-7-methyl-5-phenyl-1,2,4-oxadiazepin-3(2H)-one 

Downstream Products

• 27955-44-8 2-mercapto-4-methyl-6-phenylpyrimidine 
• 90185-77-6 N,N-dimethyl-2-(4'-methyl-6'-phenylpyrimidin-2'-yloxy)ethylamine 
• 90185-73-2 N-(2'-dimethylaminoethyl)-4-methyl-6-phenylpyrimidin-2-amine 

Relevant academic research and scientific papers

Microwave-expedited one-pot, two-component, solvent-free synthesis of functionalized pyrimidines

The synthesis of a series of diversely substituted pyrimidines under solvent-free conditions in good yields is described. Under microwave irradiation, a variety of nucleophilic substrates containing the N?C?N unit with ?-dicarbonyl compounds, ethyl cyanoacetate, malononitrile, and chalcones was cyclized to give pyrimidines. A combinatorial type approach for a one-step synthesis has been developed where a ring-closing condensation is followed by spontaneous aromatization to afford 28 functionalized and aryl/alkyl substituted pyrimidines. CSIRO 2007.

REACTIVITY OF 4,7-DIHYDRO-5-PHENYL-1,2,4-OXADIAZEPIN-3(2H)-ONES

The reactions of 4,7-dihydro-5-phenyl-1,2,4-oxadiazepin-3(2H)-ones have been studied.The behaviour of this unsaturated, seven-membered heterocyclic series, which possesses an O-NH-CO-NH functionality, depends on the reagents employed, the experimental con