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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711396Generated: October 30, 2026

2,4-Dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidine → 2-Chlorobenzo[4,5]thieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/711396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidineHCID 118340299—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chlorobenzo[4,5]thieno[2,3-d]pyrimidineHCID 9188461838.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of 2,4-dichloro-5-(2-((trichloromethyl)thio)phenyl)pyrimidine (0.618 g, 1.650 mmol) and copper(I) iodide (0.031 g, 0.165 mmol) in DMF (24.63 ml) was degassed with nitrogen and heated at 110° C. overnight. The reaction solution was cooled to room temperature, diluted with water and filtered. The resulting brown solids were washed with water and a small volume of EtOH. The aqueous layer was extracted twice with EtOAc, combined with the solids, and concentrated in vacuo. The crude product was purified by column chromatography on silica gel, eluted with 10-20% EtOAc/heptanes (v/v), affording 0.14 g (38% yield) of the 2-chlorobenzo[4,5]thieno[2,3-d]pyrimidine as white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181270B2
Source datasetuspto-grants-2015_11
ORD IDord-fca663239ad443d5b3f0140c3f657992
Source noteuspto-grants-2015_11