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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520347Generated: October 26, 2026

Nitrogen → 1-(Benzyloxy)-7-methoxy-3-(pyridin-3-yl)isoquinoline

https://huagongshe.com/reaction/1520347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Benzyloxy)-3-chloro-7-methoxyisoquinolineHCID 86677073—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-(Benzyloxy)-7-methoxy-3-(pyridin-3-yl)isoquinolineHCID 67298022—

Reaction Conditions

Temperature120 °C

Reaction Steps

1-(Benzyloxy)-7-methoxy-3-(pyridin-3-yl)isoquinoline was prepared using Method N2. 1-(Benzyloxy)-3-chloro-7-methoxyisoquinoline (93 mg, 0.5 mmol, 1.0 eq.), potassium carbonate (357 mg, 2.5 mmol, 5.0 eq.), and Pd(PPh3)2Cl2 (18 mg, 0.026 mmol, 0.05 eq.) was dissolved in the mixed solvent of 1,4-dioxane (3 mL) and water (1 mL). The resulting mixture was stirred at 120° C. for 30 min under the microwave condition. The solid was filtrated off and the filtrate was concentrated. The residue was partitioned between ethyl acetate and water. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate. After filtration and evaporation, the residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=1:10) to afford 100 mg of xxxviii-a as a yellow solid (84.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073890B2
Source datasetuspto-grants-2015_07
ORD IDord-887030c17af640a891c6bf8801b8fd64
Source noteuspto-grants-2015_07