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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylate | HCID 66874950 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Amino-2-phenethylbenzo[f][1,7]naphthyridin-8-yl)methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466167B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-cf335070a7ea40278d1494f9cbe53978 |
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| Source note | uspto-grants-2013_06 |
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