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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748414Generated: October 26, 2026

Diethyl Malonate → 2-(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetamide

https://huagongshe.com/reaction/1748414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant18-Crown-6HCID 28557—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantEthyl 2-(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetateHCID 90416945—
Reactant3-Bromo-7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridineHCID 90417593—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product2-(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetamideHCID 8629684953.8%

Reaction Conditions

Temperature115 °C

Reaction Steps

Ethyl 2-(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetate. 3-Bromo-7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridine (3.20 g, 9.11 mmol), Pd2(dba)3 (41.72 mg, 0.05 mmol), tri-tert-butylphosphonium tetrafluoroborate (290.84 mg, 1 mmol), potassium phosphate (5.42 g, 25.52 mmol), 1,4,7,10,13,16-hexaoxacyclooctadecane (1.2 g, 4.56 mmol), and diethyl malonate (9.17 mL, 60.15 mmol) were added to a microwave vial, which was capped and purged with nitrogen for several minutes then heated to 115° C. for 19 h. The reaction was cooled to ambient temperature then water and EtOAc were added. The layers were separated and the aqueous solution was extracted with EtOAc and DCM. The combined organic layers were washed with brine then dried (Na2SO4). The solvent was removed under reduced pressure. Purification (FCC, SiO2, 0-70%, EtOAc/hexanes) afforded the title compound as a pure beige solid (1.76 g, 53.8%). 1H NMR (400 MHz, CDCl3) δ 8.84 (dd, J=18.1, 2.5 Hz, 2H), 8.27 (d, J=1.4 Hz, 1H), 7.68 (d, J=2.6 Hz, 1H), 7.47-7.30 (m, 1H), 7.26-7.17 (m, 2H), 5.20 (s, 2H), 4.22 (q, J=7.2 Hz, 2H), 3.86 (s, 2H), 1.30 (t, J=7.2 Hz, 3H). [M+H]=359.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150572B2
Source datasetuspto-grants-2015_10
ORD IDord-68ac2049d3a24f4a85db2e2e369222bd
Source noteuspto-grants-2015_10