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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627431Generated: October 26, 2026

4-Chloroaniline → 2-chloro-N-(4-chlorophenyl)-6-phenylpyrimidin-4-amine

https://huagongshe.com/reaction/1627431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant2,4-Dichloro-6-(2-chloro-6-fluorophenyl)pyrimidineHCID 86661471—
SolventTetrahydrofuranHCID 8028—
Product2-chloro-N-(4-chlorophenyl)-6-phenylpyrimidin-4-amineHCID 86661473—

Reaction Steps

To 1 mmol of 2,4-dichloro-6-phenylpyrimidine (X) and 4-chloroaniline in 4 mL of dry THF was added 1 mmol (0.5 mL, 2M in THF/heptane/ethylbenzene) of lithium diisopropylamide. The reaction was followed by TLC (30% ethyl acetate/hexane). The reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate and the organic layers were dried over magnesium sulfate and concentrated under reduced pressure. The mixture was purified by chromatography on silica gel with elution by 30% ethyl acetate/hexanes to afford 70 mg of 2-chloro-N-(4-chlorophenyl)-6-phenylpyrimidin-4-amine (XII) as an amorphous solid. ESI/MS 315.883, 317.915 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785630B2
Source datasetuspto-grants-2014_07
ORD IDord-e0d78f250639415aa0b04bf8a9d74a7c
Source noteuspto-grants-2014_07