Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340257Generated: October 30, 2026

Triethylamine → 10-Methylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
Reactant1-Ethoxy-4-ethynylbenzeneHCID 2775124—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product10-Methylbenzo[f][1,7]naphthyridin-5-amineHCID 582137204%
Product3-Chloro-5-((4-ethoxyphenyl)ethynyl)picolinonitrileHCID 66875303—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a round bottom flask capped with septa was added 1-ethoxy-4-ethynylbenzene (1.1 eq), 3,5-dichloropicolinonitrile (1 eq.), triethylamine (5 eq.), and anhydrous DMF (0.2 M). Vacuumed and nitrogen flushed for three times. CuI (0.05 eq.) and bis(triphenylphosphine)dichloro-palladium(II) (0.05 eq) were added. The septum was replaced with a refluxing condenser and the flask was heated at 60° C. overnight under nitrogen atmosphere. Upon completion of the reaction as monitored by TLC, the content of the flask was loaded onto a large silica gel column pretreated with hexanes. Flash chromatography (silica gel, hexanes:EtOAc (1:4%)) afforded the product 3-chloro-5-((4-ethoxyphenyl)ethynyl)picolinonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-630d7d59737e4a09941112bb9e012795
Source noteuspto-grants-2014_11