Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340303Generated: October 30, 2026

1-(5-Aminobenzo[f][1,7]naphthyridin-8-yl)ethanol → 1-(5-Aminobenzo[f][1,7]naphthyridin-8-yl)ethanone

https://huagongshe.com/reaction/340303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Aminobenzo[f][1,7]naphthyridin-8-yl)ethanolHCID 58213697—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product1-(5-Aminobenzo[f][1,7]naphthyridin-8-yl)ethanoneHCID 58213527—

Reaction Steps

A solution 1-(5-aminobenzo[f][1,7]naphthyridin-8-yl)ethanol (from Example 88) (1.0 eq.) and activated MnO2 (20 eq.) in DCM (0.1 M) was stirred at ambient temperature over night. The reaction mixture was diluted with DCM. The MnO2 was filtered off, and the filtrate was concentrated en vacuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-5% MeOH/DCM to give 1-(5-aminobenzo[f][1,7]naphthyridin-8-yl)ethanone as a yellow solid: 1H NMR (acetone-d6): δ 9.11 (dd, 1H), 8.99 (dd, 1H), 8.56 (d, 1H), 8.20 (d, 1H), 7.94-7.88 (m, 2H), 6.90 (br s, 2H), 2.70 (s, 3H). LRMS [M+H]=238.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-161c795cbcab45a4973f552c889a6a17
Source noteuspto-grants-2014_11