4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

Base Information

Chemical Name:4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol
CAS No.:1616087-50-3
Molecular Formula:C₁₉H₁₂BrCl₂N₃S
Molecular Weight:465.2
Hs Code.:

Synonyms:4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

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Chemical Property of 4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

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Technology Process of 4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

There total 3 articles about 4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol 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: 76.0%

: 1616087-35-4
C₁₈H₁₀BrCl₂NO

: 17356-08-0
thiourea

: 1616087-50-3
4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

Guidance literature:: With potassium hydroxide; In ethanol; for 6h; Reflux; Inert atmosphere;
DOI:10.1016/j.bmcl.2014.05.002

Reference yield:

: 73568-41-9
2,6-dichloroquinoline-3-carbaldehyde

: 1616087-50-3
4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / 24 h / Inert atmosphere

2: potassium hydroxide / ethanol / 6 h / Reflux; Inert atmosphere

With potassium hydroxide; In ethanol; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.bmcl.2014.05.002

Reference yield:

: 2142-63-4
1-(3-Bromophenyl)ethanone

: 1616087-50-3
4-(3-bromophenyl)-6-(2,6-dichloroquinolin-3-yl)-1,6-dihydropyrimidine-2-thiol

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / 24 h / Inert atmosphere

2: potassium hydroxide / ethanol / 6 h / Reflux; Inert atmosphere

With potassium hydroxide; In ethanol; 1: |Claisen-Schmidt Condensation;
DOI:10.1016/j.bmcl.2014.05.002