17730-53-9

Usage

InChI:InChI=1/C10H10N2OS/c1-11-8-6-4-3-5-7(8)9(13)12(2)10(11)14/h3-6H,1-2H3

Upstream product

• 119-68-6 N-Methylanthranilic acid 
• 556-61-6 methyl thioisocyanate 
• 74-88-4 methyl iodide 
• 98322-26-0 Potassium salt of 1-methyl-2-thioxo-4-quinazolone 
• 98322-24-8 C₉H₇N₂OS^(1-)*Na⁽¹⁺⁾ 
• 1419176-20-7 CF₃O₃S^(1-)*C₁₀H₁₁N₂O⁽¹⁺⁾ 
• 118-92-3 anthranilic acid 
• 491-36-1 4-Hydroxyquinazoline 
• 2436-66-0 3-methylquinazolin-4(3H)-one 
• 1419176-14-9 C₁₀H₁₁N₂O⁽¹⁺⁾*BF₄^(1-) 
• 10328-92-4 N-Methylisatoic anhydride 
• 98322-25-9 C₉H₇N₂OS^(1-)*Li⁽¹⁺⁾ 
• 80-48-8 methyl p-toluene sulfonate 
• 98322-27-1 1-Methyl-2-thioxo-2,3-dihydro-1H-quinazolin-4-one; compound with triethyl-amine 

Relevant academic research and scientific papers

A new mixed amino-amido N-heterocyclic carbene based on anthranilic acid

The synthesis of a new mixed amino-amido N-heterocyclic carbene (type A) starting from anthranilic acid is presented. A new straightforward synthetic approach to related diaminocarbenes of type B is also described. Both NHCs react with group 6 elements to form heteroureas and coordinate to L2ClM fragments (M = Rh, Ir; L2 = COD, (CO)2). IR spectroscopic analysis of the carbonyl complexes reveals that the diamino-NHC is a better donor ligand (TEP: 2054 cm-1) compared to the amino-amido NHC (TEP: 2060 cm-1). In line with this behavior, a carbene dimerization to give the corresponding olefin is observed only for derivatives of type A. X-ray structure determinations are reported for two Rh complexes of ligand A and its cationic precursor.

ALKYLATION OF THE SALTS OF 1-METHYL-2-THIOXOQUINAZOLIN-4-ONES

During the alkylation of 1-methyl-2-thioxoquinozolin-4-one the methyl group adds mainly at the N3 atom.In the case of the "hard" alkylating agent methyl p-toluenesulfonate the reaction hardly depends at all on the nature of the counterion and the solvent.

A Mass Spectral Rearrangement of 2-(Alkylamino)benzoic Acid Derivatives and Related Heterocyclic Systems

The behavior of a series of 2-(alkylamino)benzoic acid derivatives and related heterocyclic systems has been investigated using electron impact mass spectrometry and fragmentation pathways have been formulated.Deuterium-labeled and 13C-labeled compounds w

SYNTHESIS AND SPECTRAL EXAMINATION OF THE POSITION OF TAUTOMERIC EQUILIBRIUM IN 2-THIOXO-4-QUINAZOLONE

2-Thioxo-4-quinazolone and its derivatives mono- and dimethylated at ring atoms N(1) and N(3) and the exocyclic sulfur have been synthesized.Using model compounds, UV spectroscopy has been used to show that 2-thioxo-4-quinazolone exists in the thioketo-form, no appreciable amounts of the thiol or enol isomers being present.