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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259177Generated: November 2, 2026

Sodium Carbonate → Methyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylate

https://huagongshe.com/reaction/1259177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(Tert-butoxycarbonylamino)-4-(methoxycarbonyl)phenylboronic acidHCID 66875237—
Reactant(E)-3-chloro-5-styrylpicolinonitrileHCID 66875239—
Reactant2-Chloro-6-phenethylnicotinonitrileHCID 85682759—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventToluene ethanolHCID 21863594—
ProductMethyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylateHCID 66874950—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 2-(tert-butoxycarbonylamino)-4-(methoxycarbonyl) phenylboronic acid (from Example 85/Step1) (1.0 eq.) and 2-chloro-6-phenethylnicotinonitrile (prepared from (E)-3-chloro-5-styrylpicolinonitrile (from Example 32/Step 1) following the procedure described in Example 114/Step3) (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 mixture was diluted with EtOAc and water. The two phases were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-60% EtOAc/Hexanes to give methyl 5-amino-2-phenethylbenzo[f][1,7]naphthyridine-8-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-3aeb667e4f0347309063d5e494a64cf2
Source noteuspto-grants-2013_06