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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944609Generated: November 1, 2026

Trimethylsilyl iodide → HCID 67008298, compound

https://huagongshe.com/reaction/1944609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 67008365HCID 67008365—
SolventDichloromethaneHCID 6344—
ProductHCID 67008298HCID 6700829814.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of compound 7.0 1-(3-chloro-4-fluorophenyl)-9-(6-methoxypyridin-3-yl)benzo[h][1,6]naphthyridin-2(1H)-one (21 mg, 0.05 mmol, 1 equiv.) in CH2Cl2(2 mL) at room temperature was added TMSI (70 μL, 0.5 mmol, 10 equiv.). The resulting solution was stirred at 50° C. for 48 h before being cooled to room temperature and quenched with Na2CO3 (sat. 2 mL). After separation, the organic phase was dried over Na2SO4 and evaporated under vacuum. The residue was diluted with DMF (2 mL) and purified via preparative LC-MS (CH3CN: H2O) to afford the desired product 7.1 1-(3-chloro-4-fluorophenyl)-9-(6-oxo-1,6-dihydropyridin-3-yl)benzo[h][1,6]naphthyridin-2(1H)-one (3 mg). LC-MS (M+H): 417.07

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394818B2
Source datasetuspto-grants-2013_03
ORD IDord-f3f5ae95a2454ac9873dcd511ecb4381
Source noteuspto-grants-2013_03