Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340231Generated: October 29, 2026

(E)-2-styrylbenzo[f][1,7]naphthyridin-5-amine → 2-Phenethylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2-styrylbenzo[f][1,7]naphthyridin-5-amineHCID 58213554—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product2-Phenethylbenzo[f][1,7]naphthyridin-5-amineHCID 44230627—

Reaction Steps

To a solution of (E)-2-styrylbenzo[f][1,7]naphthyridin-5-amine (Example 32) in ethyl acetate/methanol (1:4, 0.05 M) was added 10% wt palladium on carbon (0.2 eq.). Hydrogen gas was introduced via a balloon, and the reaction was stirred for 3 hours. The mixture was filtered through a pad of celite, washing with dichloromethane. The filtrate was concentrated en vacuo and the crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give 2-phenethylbenzo[f][1,7]naphthyridin-5-amine as a yellow solid. 1H NMR (CDCl3): δ 8.54 (d, 1H), 8.32 (d, 1H), 8.10 (dd, 1H), 7.63 (dd, 1H), 7.51 (m, 1H), 7.03-7.32 (m, 6H), 6.16 (bs, 2H), 3.11 (t, 2H), 2.97 (t, 2H). LRMS [M+H]=300.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-9600f4361150424885d39a13bcee9238
Source noteuspto-grants-2014_11