Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340301Generated: October 26, 2026

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

https://huagongshe.com/reaction/340301

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 vacuo 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 numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-7a349b30b8cb4ab19eccfeb30937a8a5
Source noteuspto-grants-2014_11