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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167652Generated: October 29, 2026

Tetraethyl methylenediphosphonate → (E)-diethyl 2-(5-amino-2-(4-methoxy-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)vinylphosphonate

https://huagongshe.com/reaction/2167652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethyl methylenediphosphonateHCID 15455—
ReactantSodium hydrideHCID 24758—
Reactant5-Amino-2-(4-methoxy-2-methylphenethyl)benzo[f][1,7]naphthyridine-8-carbaldehydeHCID 58166518—
SolventTetrahydrofuranHCID 8028—
Product(E)-diethyl 2-(5-amino-2-(4-methoxy-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)vinylphosphonateHCID 86651453—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of NaH (1.2 equiv.) in THF (0.1 M) cooled at 0° C. was added a solution of tetraethyl methylenediphosphonate (1.3 equiv.) in THF (0.21 M). To the resulting reaction mixture was added a solution of 5-amino-2-(4-methoxy-2-methylphenethyl)benzo[f][1,7]naphthyridine-8-carbaldehyde (2-2) (Example 9—Step 1) (1.0 equiv.) in THF (0.08 M). The reaction was stirred at room temperature for 30 minutes, then solvents were removed in vacuo, and the resulting residue was purified by a COMBIFLASH® system (ISCO) using a gradient of 0-5% MeOH/DCM to provide (E)-diethyl 2-(5-amino-2-(4-methoxy-2-methylphenethyl)benzo[f][1,7]naphthyridin-8-yl)vinylphosphonate (3-1) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045470B2
Source datasetuspto-grants-2015_06
ORD IDord-6054d67dffec407ea3325d3b880e74a5
Source noteuspto-grants-2015_06