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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259178Generated: October 31, 2026

Methyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylate → (5-Amino-2-phenethylbenzo[f][1,7]naphthyridin-8-yl)methanol

https://huagongshe.com/reaction/1259178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylateHCID 66874950—
SolventTetrahydrofuranHCID 8028—
Product(5-Amino-2-phenethylbenzo[f][1,7]naphthyridin-8-yl)methanolHCID 58213577—

Reaction Steps

To a solution of methyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylate (from the previous step) (1.0 eq.) in THF (0.03M) was added Super-H (10 eq.) at 0° C. The solution was allowed to warm to ambient temperature over 30 min The reaction was quenched by water until no bubbling. The layers were separated and aqueous layer was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4 and 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-amino-2-phenethylbenzo[f][1,7]naphthyridin-8-yl)methanol as an off white solid: 1H NMR (methanol-d4): δ 8.63 (dd, 1H), 8.56 (dd, 1H), 8.24 (d, 1H), 7.57 (d, 1H), 7.35 (dd, 1H), 7.27-7.15 (m, 5H), 4.75 (s, 2H), 3.20 (t, 2H), 3.06 (t, 2H). LRMS [M+H]=330.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-cf335070a7ea40278d1494f9cbe53978
Source noteuspto-grants-2013_06