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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340228Generated: October 25, 2026

Sodium Carbonate → 2-Phenylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(2-BOC-aminophenyl)boronic acidHCID 2773226—
Reactant3-Chloro-5-phenylpicolinonitrileHCID 66875522—
SolventMethanolHCID 887—
SolventToluene ethanolHCID 21863594—
Product2-Phenylbenzo[f][1,7]naphthyridin-5-amineHCID 58213717—

Reaction Steps

A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-chloro-5-phenylpicolinonitrile (from step 1) (1.0 eq.), tetrakis(triphenyl-phosphine)palladium (5 mol %), and 2N aqueous sodium carbonate solution (2.0 eq.) in toluene/ethanol (2:1, 0.03 M) was stirred at 100° C. overnight. After cooling to ambient temperature, the reaction content was diluted with methanol. The insoluble solids were filtered off, and the filtrate was concentrated en vacuo to obtain a crude residue. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give 2-phenylbenzo[f][1,7]naphthyridin-5-amine as a white solid. 1H NMR (dmso-d6): δ 9.13 (d, 1H), 9.03 (d, 1H), 8.56 (d, 1H), 7.98 (d, 2H), 7.43-7.56 (m, 5H), 7.27 (m, 1H), 7.13 (bs, 2H). LRMS [M+H]=272.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-e3446919bd0347dbb0474b74fa71e01b
Source noteuspto-grants-2014_11