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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798505Generated: October 29, 2026

Acetonitrile → N-[1-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-1-methyl-ethyl]-acetamide

https://huagongshe.com/reaction/1798505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium HydroxideHCID 14798—
Reactant2-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-propan-2-olHCID 68735197—
SolventDichloromethaneHCID 6344—
ProductN-[1-(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-1-methyl-ethyl]-acetamideHCID 68733910—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 2-(5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-propan-2-ol (Example 2.80; step1) (1 eq, 0.135 mmol, 50 mg) in acetonitrile (2 ml) is added tetrafluoroboric acid diethyl ether complex (3.5 eq, 0.473 mmol, 0.06 ml) and the reaction mixture is heated at 85° C. overnight. The pH of the reaction mixture is adjusted to 8-9 by addition of sodium hydroxide (2M). The solution is dissolved in DCM and washed with water. The combined organic extracts are washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title compound; [M+H]+ 411/413

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343966B2
Source datasetuspto-grants-2013_01
ORD IDord-e564add6a80b4a4089ac927f528a45f2
Source noteuspto-grants-2013_01