61433-76-9

Upstream product

• 2835-99-6 4-amino-3-methylphenol 
• 39495-15-3 4-acetamido-3-methylphenol 
• 100-44-7 benzyl chloride 

Downstream Products

• 196616-56-5 2-carboxy-3,7-dimethyl-5-benzyloxyindole 
• 196616-57-6 5-Benzyloxy-3,7-dimethyl-1H-indole 
• 196616-42-9 3,7-Dimethyl-1H-indole-4,5-dione 
• 4792-60-3 2-methyl-4-benzyloxyaniline 

Relevant academic research and scientific papers

Synthesis, physicochemical properties, and amide-oxidation reaction of indolequinone derivatives as model compounds of novel organic cofactor TTQ of amine dehydrogenases

3,4-Disubstituted 6,7-indolequinones [1,3-dimethyl]-4-(3'-methylindol- 2'-yl)indole-6,7-dione (2), 3-methyl-4-phenylindole-6,7-dione (3), and 3,4- dimethyl-6,7-dione (4)] and a 3,7-disubstituted 4,5-indolequinone [3,7- dimethylindole-4,5-dione (5)] have been synthesized as models for the novel organic cofactor TTQ bacterial amine dehydrogenases. The substituent and structural effects on the physicochemical properties of the quinones have been investigated in detail by comparing the spectroscopic data (UV-vis, IR, 1H- and 13C-NMR), pK(a) values of the pyrrole proton, and the two-electron redox potentials with those of model compound 1 [3-methyl-4-(3'-methylindol- 2'-yl)indole-6,7-dione] previously reported (ref 5). Reactivity of each quinone in the transamination process [iminoquinone formation (k1), rearrangement to product-imine (k2) and aminophenol formation (k3)] has been investigated kinetically, revealing that the substituent and structural effects on the amine-oxidation reaction are not significant. In the aerobic catalytic oxidation of benzylamine, however, the aromatic substituents on the quinone ring play an important role to protect the quinone from the deactivation process of a Michael-type addition by the amine, making it act as an efficient turnover catalyst.

Derivatives of 2-substituted-hydroxyanilino-hexahydro-2H-benzo[α]quinolizines

2-Substituted-hydroxyanilino-hexahydro-2H-benzo[α]quinolizines of the structural formula, SPC1 In which R1 is a hydrogen atom or an alkanoyl group of 2 to 4 carbon atoms and each of substituents R2, R3, R4, R5, and R6 is a hydrogen atom, a hydroxyl, or a methyl group, such that at least one of the latter substituents is a hydroxyl group, exhibit coronary vasodilating activity.