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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844036Generated: October 25, 2026

1,4-Dioxane → 2-(4-cyclopropylpyridin-3-yl)-7-(trifluoromethyl)-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/1844036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant7-(Trifluoromethyl)-3,4-dihydroisoquinolin-1(2H)-oneHCID 66801593—
Reactant4-Cyclopropyl-3-iodopyridineHCID 66801887—
CatalystCopper iodideHCID 83717—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-(4-cyclopropylpyridin-3-yl)-7-(trifluoromethyl)-3,4-dihydroisoquinolin-1(2H)-oneHCID 5694305512.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

7-(trifluoromethyl)-3,4-dihydroisoquinolin-1(2H)-one (I-4-d: 100 mg, 0.465 mmol) was reacted with 4-cyclopropyl-3-iodopyridine (I-73c: 125.3 mg, 0.51 mmol), 1,4-dioxane (5 mL), copper iodide (8.8 mg, 0.0465 mmol), trans-N,N′-dimethyl-cyclohexyl-1,2-diamine (6.6 mg, 0.0465 mmol) and potassium phosphate (246 mg, 1.16 mmol). The resulting mixture was stirred for 24 hours at 120° C. The reaction was monitored by TLC (10% methanol in CHCl3). The reaction mixture was concentrated to afford the crude product. Purification by column chromatography on silica gel (2% methanol in CHCl3), followed by preparative HPLC afforded 20 mg of the product (12.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-fb71b6cd3f614efd9c5ebf1f070b470d
Source noteuspto-grants-2015_02