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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479589Generated: October 27, 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/1479589

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 vaccuo 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 numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-4e1a6d3efbef415da6d5bf4d098750ae
Source noteuspto-grants-2016_08