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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852966Generated: November 1, 2026

N,N-Diethylaniline → HCID 86685301, compound

https://huagongshe.com/reaction/1852966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiethylanilineHCID 7061—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 67457657HCID 67457657—
SolventAcetonitrileHCID 6342—
ProductHCID 86685301HCID 8668530139%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a flask charged with 7-(4-bromophenyl)imidazo[1,2-c]pyrimidin-5(6H)-one (25.00 g, 86.173 mmol), phosphoryl trichloride (31.554 mL, 344.69 mmol), and N,N-diethylaniline (27.420 mL, 172.35 mmol) was added acetonitrile (200 mL) and the mixture was heated to 50° C. overnight. The reaction mixture was concentrated under reduced pressure and the residue diluted with water and DCM. The aqueous was neutralized with potassium carbonate and the bi-phasic mixture passed through a pad of celite to remove the insoluble material. The layers were separated and the aqueous extracted with DCM. The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The crude material was triturated with hexanes and the solids were collected by filtration to afford 7-(4-bromophenyl)-5-chloroimidazo[1,2-c]pyrimidine (10.369 g, 33.604 mmol, 38.997% yield). MS (apci) m/z=310.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962596B2
Source datasetuspto-grants-2015_02
ORD IDord-f6b8bc0a647b480789c69f9d909b3143
Source noteuspto-grants-2015_02