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

Base Information

Chemical Name:N-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide
CAS No.:1059734-18-7
Molecular Formula:C₃₂H₂₉N₅O
Molecular Weight:499.615
Hs Code.:

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

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

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

There total 7 articles about N-{5-[(cyclopropylamino)methyl]-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: 52.0%

: 1059733-71-9
N-(5-formyl-2-methylphenyl)-4-[(4-phenylquinazolin-2-yl)amino]benzamide

: 765-30-0
Cyclopropylamine

: 1059734-18-7
N-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: N-(5-formyl-2-methylphenyl)-4-[(4-phenylquinazolin-2-yl)amino]benzamide; Cyclopropylamine; With acetic acid; In tetrahydrofuran; dichloromethane; at 20 ℃; for 1h;

With sodium tris(acetoxy)borohydride; In tetrahydrofuran; dichloromethane;

Reference yield:

: C₃₀H₂₄N₄O₃

: 1059734-18-7
N-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide; water / tetrahydrofuran; methanol / 3 h / 70 °C

1.2: pH 5

2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: diisobutylaluminium hydride / dichloromethane / 1.5 h / -78 °C

4.1: acetic acid / tetrahydrofuran; dichloromethane / 1 h / 20 °C

With sodium hydroxide; water; diisobutylaluminium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1059733-47-9
4-methyl-3-[({4-[(4-phenylquinazolin-2-yl)amino]phenyl}carbonyl)amino]benzoic acid

: 1059734-18-7
N-{5-[(cyclopropylamino)methyl]-2-methylphenyl}-4-[(4-phenylquinazolin-2-yl)amino]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

2: diisobutylaluminium hydride / dichloromethane / 1.5 h / -78 °C

3: acetic acid / tetrahydrofuran; dichloromethane / 1 h / 20 °C

With diisobutylaluminium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;