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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843963Generated: October 25, 2026

Potassium Phosphate, Tribasic → 8-Fluoro-2-(4-methylpyridine-3-yl) 3,4-dihydro-2H-benzo[4,5]thieno[3,2-c]pyridin-1-one

https://huagongshe.com/reaction/1843963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Iodo-4-methylpyridineHCID 14423513—
Reactant7-Chloro-2-pyridin-3-yl-3,4-dihydro-2H-isoquinolin-1-oneHCID 56942726—
Reactant8-fluoro-3,4-dihydro-2H-benzo[4,5]thieno[3,2-c]pyridin-1-oneHCID 89964175—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
Product8-Fluoro-2-(4-methylpyridine-3-yl) 3,4-dihydro-2H-benzo[4,5]thieno[3,2-c]pyridin-1-oneHCID 5694097667.37%

Reaction Steps

Using analogous conditions and workup as described for the preparation of Compound 1A, 8-Fluoro-3,4-dihydro-2H-benzo[4,5]thieno[3,2-c]pyridin-1-one (I-50 g: 100 mg, 0.452 mmol) was reacted with 3-iodo-4-methylpyridine (99.09 mg, 0.452 mmol), 1,4-dioxane (5 mL), copper iodide (8.64 mg, 0.0452 mmol), trans-N,N′-dimethyl-cyclohexyl-1,2-diamine (19.25 mg, 0.1356 mmol) and potassium phosphate (287.44 mg, 1.356 mmol) at 115° C. overnight under nitrogen atmosphere to afford the crude product. Purification by column chromatography on silica gel (1.5% methanol in CHCl3) afforded 95 mg of the product (67.37% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-c3cb0b60a6b047cfba052866f37376d1
Source noteuspto-grants-2015_02