4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

Base Information

Chemical Name:4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide
CAS No.:1266584-28-4
Molecular Formula:C₂₃H₂₇Cl₂N₅O
Molecular Weight:460.406
Hs Code.:

Synonyms:4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

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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 4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

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Technology Process of 4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

There total 7 articles about 4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide 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: 69.0%

: 1266584-24-0
N¹-(2-(2-amino-4-chlorophenyl)quinazolin-4-yl)-N³,N³-dimethylpropane-1,3-diamine

: 4635-59-0
4-Chlorobutanoyl chloride

: 1266584-28-4
4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

Guidance literature:: With potassium carbonate; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.ejmech.2011.10.057

Reference yield:

: 1266584-22-8
N¹-(2-(4-chloro-2-nitrophenyl)quinazolin-4-yl)-N³,N³-dimethylpropane-1,3-diamine

: 1266584-28-4
4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrazine hydrate / isopropyl alcohol / 2 h / Reflux

2: potassium carbonate / dichloromethane / 0 - 20 °C

With palladium 10% on activated carbon; potassium carbonate; hydrazine hydrate; In dichloromethane; isopropyl alcohol;
DOI:10.1016/j.ejmech.2011.10.057

Reference yield:

: 349135-17-7
N-(2-carbamoylphenyl)-4-chloro-2-nitrobenzamide

: 1266584-28-4
4-chloro-N-(5-chloro-2-(4-(3-(dimethylamino)propylamino)quinazolin-2-yl)phenyl)butanamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hydroxide / ethanol; water / 2 h / Reflux

2: N,N-diethylaniline; trichlorophosphate / toluene / 6 h / 80 °C

3: tetrahydrofuran / 5 h / Inert atmosphere; Reflux

4: palladium 10% on activated carbon; hydrazine hydrate / isopropyl alcohol / 2 h / Reflux

5: potassium carbonate / dichloromethane / 0 - 20 °C

With palladium 10% on activated carbon; potassium carbonate; hydrazine hydrate; N,N-diethylaniline; potassium hydroxide; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; water; isopropyl alcohol; toluene;
DOI:10.1016/j.ejmech.2011.10.057