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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340241Generated: October 30, 2026

3-Chloro-1-methylbenzo[f][1,7]naphthyridin-5-amine → 1-Methylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1-methylbenzo[f][1,7]naphthyridin-5-amineHCID 86652348—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product1-Methylbenzo[f][1,7]naphthyridin-5-amineHCID 58213725—

Reaction Steps

To a solution of 3-chloro-1-methylbenzo[f][1,7]naphthyridin-5-amine (from step 3) in ethyl acetate/methanol (1:2, 0.03 M) was added 10% wt palladium on carbon (0.2 eq.). The reaction vessel was shaken on a hydrogen Pan apparatus under 50 psi of hydrogen overnight. The mixture was filtered through a pad of celite, washing with dichloromethane. The filtrate was concentrated en vacuo and purified by a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give 1-methylbenzo[f][1,7]naphthyridin-5-amine as a white solid. 1H NMR (CDCl3): δ 8.63 (d, 1H), 8.44 (d, 1H), 7.71 (dd, 1H), 7.54 (m, 1H), 7.45 (d, 1H), 7.30 (m, 1H), 6.20 (bs, 2H), 3.01 (s, 3H). LRMS [M+H]=210.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-e41fccc3622e4752822838ed2eeaa446
Source noteuspto-grants-2014_11