C₁₅H₁₆N₂O

Base Information

• Chemical Name: C₁₅H₁₆N₂O
• CAS No.: 339289-82-6
• Molecular Formula: C₁₅H₁₆N₂O
• Molecular Weight: 240.305
• Mol file: 339289-82-6.mol

Synonyms:

Chemical Property of C₁₅H₁₆N₂O

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

Technology Process of C₁₅H₁₆N₂O

There total 1 articles about C₁₅H₁₆N₂O 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:

6-methyl-1H-benzo[d][1,3]oxazine-2,4-dione (4692-99-3) + benzylamine (100-46-9) → C15H16N2O (339289-82-6)

Guidance literature:

In toluene; at 100 ℃; regioselective reaction; Sealed tube;

DOI:10.1039/c4ob00484a

Reference yield: 62.0%

mucobromic acid (488-11-9) + C15H16N2O (339289-82-6) → N-benzyl-2,9-dimethyl-6-oxo-5,6-dihydrodibenzo[b,h][1,6]-naphthyridine-11-carboxamide

Guidance literature:

With iodine; In tetrahydrofuran; for 12h; Reflux;

DOI:10.1039/c5ob02620b

Reference yield:

tert-butylisonitrile (119072-55-8,7188-38-7) + C15H16N2O (339289-82-6) → 3-benzyl-2-(tert-butylamino)-6-methylquinazolin-4(3H)-one (1618654-41-3)

Guidance literature:

With palladium diacetate; silver carbonate; In toluene; at 100 ℃; for 24h; regioselective reaction; Sealed tube;

DOI:10.1039/c4ob00484a

upstream raw materials:

6-methyl-1H-benzo[d][1,3]oxazine-2,4-dione

benzylamine

Downstream raw materials:

3-benzyl-2-(tert-butylamino)-6-methylquinazolin-4(3H)-one