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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479536Generated: November 1, 2026

Sodium Carbonate → (E)-8-methyl-2-(prop-1-enyl)benzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/1479536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactanttert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamateHCID 46737997—
Reactant(E)-3-chloro-5-(prop-1-enyl)picolinonitrileHCID 66893384—
SolventMethanolHCID 887—
SolventToluene ethanolHCID 21863594—
Product(E)-8-methyl-2-(prop-1-enyl)benzo[f][1,7]naphthyridin-5-amineHCID 66890437—

Reaction Steps

A solution of tert-butyl 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from Example 5/Step 2) (1.0 eq.) and (E)-3-chloro-5-(prop-1-enyl)picolinonitrile (from the previous step) (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 vaccuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give (E)-8-methyl-2-(prop-1-enyl)benzo[f][1,7]naphthyridin-5-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-2f62143567f5434181505aa7104ed8f5
Source noteuspto-grants-2016_08