Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551562Generated: October 25, 2026

Lithium Chloride → 3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridine

https://huagongshe.com/reaction/551562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantPotassium FluorideHCID 522689—
Reactant3,7-Dibromo-1,5-naphthyridineHCID 1236658—
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridineHCID 6708234355%

Reaction Steps

A solution of 3,7-dibromo-1,5-naphthyridine (0.5 g, 1.74 mmol), tributyl-2-ethoxy-vinylstannane (1.91 mmol, 0.69 g), LiCl (8.7 mmol, 0.37 g) and 0.085 g of PdCl2(PPh3)2 in 50 mL of toluene was heated at 95° C. for 16 hr. After cooling off, 20 mL of a 2 M solution of KF was added to the mixture and stirring was continued for 0.5 hr. The mixture was diluted with 100 mL of CH2Cl2 and washed successively with a saturated solution of sodium bicarbonate, brine and water. The organic layer was dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was chromatographed using 5% MeOH in CH2Cl2 to give the desired material in 55% yield. 1H NMR (CDCl3, 300 MHz) δ 1.40 (m, 3H), 4.05 (m, 2H), 5.85 (s, 1H), 7.25 (s, 1H), 8.15 (m, 1H), 8.55 (m, 1H), 8.85 (m, 2H). MS (ESI) [M+H]+ at 280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947711B2
Source datasetuspto-grants-2011_05
ORD IDord-5b423b6b34454a69b8d93b1648e200cd
Source noteuspto-grants-2011_05