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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259113Generated: October 29, 2026

8-Methyl-2-vinylbenzo[f][1,7]naphthyridin-5-amine → 2-Ethyl-8-methylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/1259113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Methyl-2-vinylbenzo[f][1,7]naphthyridin-5-amineHCID 58213674—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product2-Ethyl-8-methylbenzo[f][1,7]naphthyridin-5-amineHCID 58213588—

Reaction Steps

To a solution of 8-methyl-2-vinylbenzo[f][1,7]naphthyridin-5-amine (from the previous step) in ethyl acetate/methanol (1:4, 0.05 M) was added 10% wt palladium on carbon (0.2 eq.). Hydrogen gas was introduced via a balloon, and the reaction was stirred for 3 hours. The mixture was filtered through a pad of celite and washed with dichloromethane. The filtrate was concentrated en vaccuo and purified by a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give 2-ethyl-8-methylbenzo[f][1,7]naphthyridin-5-amine as an off white solid. 1H NMR (CDCl3): δ 8.61 (d, 1H), 8.42 (d, 1H), 8.10 (d, 1H), 7.44 (s, 1H), 7.12 (dd, 1H), 6.00 (bs, 2H), 2.84 (q, 2H), 2.45 (s, 3H), 1.33 (t, 3H). LRMS [M+H]=238.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-b4c2f7861d9147eba263f65c4afaa811
Source noteuspto-grants-2013_06