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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479587Generated: October 30, 2026

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

https://huagongshe.com/reaction/1479587

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 numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-a31826bd039d4195b8250e0d7c0cac7e
Source noteuspto-grants-2016_08