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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259171Generated: November 3, 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/1259171

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 numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-4d56afdf4907496da581d864d9b29ac5
Source noteuspto-grants-2013_06