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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259169Generated: November 2, 2026

(5-Aminobenzo[f][1,7]naphthyridin-8-yl)methanol → 5-Aminobenzo[f][1,7]naphthyridine-8-carbaldehyde

https://huagongshe.com/reaction/1259169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Aminobenzo[f][1,7]naphthyridin-8-yl)methanolHCID 44232402—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product5-Aminobenzo[f][1,7]naphthyridine-8-carbaldehydeHCID 86652355—

Reaction Steps

A solution of (5-aminobenzo[f][1,7]naphthyridin-8-yl)methanol (from Example 85) (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 0-10% MeOH/DCM to give 5-aminobenzo[f][1,7]naphthyridine-8-carbaldehyde as a yellow solid: 1H NMR (acetone-d6): δ 10.19 (s, 1H), 9.14 (dd, 1H), 9.01 (dd, 1H), 8.63 (d, 1H), 8.14 (d, 1H), 7.93 (dd, 1H), 7.81 (dd, 1H), 6.96 (br s, 2H). LRMS [M+H]=224.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-d377f0ff52bd472fa21657818aa2a2e2
Source noteuspto-grants-2013_06