(4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

Base Information

Chemical Name:(4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester
CAS No.:86149-03-3
Molecular Formula:C₂₂H₁₂Br₂Cl₂N₂O₃S
Molecular Weight:615.129
Hs Code.:

Synonyms:(4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

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Chemical Property of (4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

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Technology Process of (4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

There total 2 articles about (4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester 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: 65.0%

: 18730-32-0
6,8-dibromo-3-(4-chloro-phenyl)-2-thioxo-2,3-dihydro-1H-quinazolin-4-one

: 4122-68-3
4-chlorophenyloxyacetyl chloride

: 86149-03-3
(4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

Guidance literature:: With sodium hydroxide; In ethanol; 2.) reflux, 6 h;
DOI:10.1002/ardp.19833160509

Reference yield:

: 122-88-3
4-Chlorophenoxyacetic acid

: 86149-03-3
(4-Chloro-phenoxy)-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 4 h / Heating

2: 65 percent / 1.) NaOH / ethanol / 2.) reflux, 6 h

With sodium hydroxide; thionyl chloride; In ethanol;
DOI:10.1002/ardp.19833160509