2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

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Chemical Name:2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide
CAS No.:1382229-33-5
Molecular Formula:C₃₄H₂₃Cl₂N₇O₄S
Molecular Weight:696.573
Hs Code.:

Synonyms:2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

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Chemical Property of 2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

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Technology Process of 2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

There total 6 articles about 2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide 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: 55.0%

: 1382229-05-1
2-((4-chloro-5-cyano-6-(4-hydroxyphenyl)pyrimidin-2-yl)sulfanyl)-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

: 62-53-3
aniline

: 1382229-33-5
2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

Guidance literature:: With triethylamine; In ethanol; at 20 ℃; for 29h; Reflux;
DOI:10.1016/j.ejmech.2012.03.050

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1382229-33-5
2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol

2: potassium carbonate / acetone / 6 h / Reflux

3: trichlorophosphate / 6.5 h / Cooling with ice; Reflux

4: triethylamine / ethanol / 29 h / 20 °C / Reflux

With potassium carbonate; triethylamine; trichlorophosphate; In ethanol; acetone;
DOI:10.1016/j.ejmech.2012.03.050

Reference yield:

: 893759-59-6
C₁₁H₇N₃O₂S

: 1382229-33-5
2-[(5-cyano-6-(4-hydroxyphenyl)-4-phenylaminopyrimidin-2-yl)sulfanyl]-N-[2-(2,4-dichlorophenoxymethyl)-4-oxo-4H-quinazolin-3-yl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 6 h / Reflux

2: trichlorophosphate / 6.5 h / Cooling with ice; Reflux

3: triethylamine / ethanol / 29 h / 20 °C / Reflux

With potassium carbonate; triethylamine; trichlorophosphate; In ethanol; acetone;
DOI:10.1016/j.ejmech.2012.03.050