Benzenamine, N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2- quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl-

Base Information

Chemical Name:Benzenamine, N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2- quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl-
CAS No.:89827-18-9
Molecular Formula:C₃₃H₃₉N₃
Molecular Weight:477.693
Hs Code.:

Benzenamine,
N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2-
quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl-

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzenamine, N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2- quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl-

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Technology Process of Benzenamine, N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2- quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl-

There total 2 articles about Benzenamine, N-[2-[3,4-dihydro-6-methyl-4-(1-methylethylidene)-3-(4-methylphenyl)-2- quinazolinyl]-2-methyl-1-(1-methylethyl)propylidene]-4-methyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 46.0%

: 18779-86-7
dimethylketene-N-p-tolylimine

: 6876-49-9
N-(4-methylphenyl)-2,2-dimethylacetamide

: 89827-18-9
2-(1,1,3-trimethyl-2-(p-tolylimino)butyl)-3-p-tolyl-4-isopropylidene-6-methyl-3,4-dihydroquinazoline

: 89827-17-8
2,4,6-triisopropylidene-1,3,5-tri-p-tolylhexahydro-1,3,5-triazine

: 52223-07-1
2-isopropyl-3-p-tolyl-4-isopropylidene-6-methyl-3,4-dihydroquinazoline

Guidance literature:: With aluminium trichloride; In dichloromethane; at -40 ℃; for 0.25h; Product distribution; other AlCl₃ ratio, temperature, reagent, reaction times; reactions of other ketene imines;
DOI:10.1021/jo00186a025