N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Base Information

Chemical Name:N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide
CAS No.:1059734-19-8
Molecular Formula:C₃₂H₃₀N₆O₂
Molecular Weight:530.629
Hs Code.:

Synonyms:N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

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Chemical Property of N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

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Technology Process of N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

There total 7 articles about N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide 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: 35.0%

: 1118-68-9
dimethylaminoacetic acid

: 1059734-15-4
N-(5-amino-2-methylphenyl)-4-[(4-phenylquinazolin-2-yl)amino]benzamide

: 1059734-19-8
N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 80 ℃; for 1h;

Reference yield:

: 23441-75-0
4-phenyl-1H-quinazolin-2-one

: 1059734-19-8
N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: trichlorophosphate / 0.5 h / 105 °C

2: isopropyl alcohol / 4 h / Heating / reflux

3: thionyl chloride / N,N-dimethyl-formamide / dichloromethane / 20 °C

4: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; dichloromethane / 20 °C

5: formic acid; potassium formate / platinum on carbon / tetrahydrofuran; ethanol / 1 h / Heating / reflux

6: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 1 h / 80 °C

With formic acid; thionyl chloride; potassium formate; N-ethyl-N,N-diisopropylamine; HATU; trichlorophosphate; platinum on carbon; N,N-dimethyl-formamide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1059735-24-8
4-(4-phenylquinazolin-2-ylamino)benzoyl chloride

: 1059734-19-8
N-{5-[(N,N-dimethylglycyl)amino]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; dichloromethane / 20 °C

2: formic acid; potassium formate / platinum on carbon / tetrahydrofuran; ethanol / 1 h / Heating / reflux

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 1 h / 80 °C

With formic acid; potassium formate; N-ethyl-N,N-diisopropylamine; HATU; platinum on carbon; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;