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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908310Generated: October 26, 2026

Potassium Carbonate → N-(6-(isoquinolin-5-yl)naphthalen-2-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/908310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIsoquinoline-5-boronic acidHCID 599474—
Reactant6-(Thiophene-2-carboxamido)naphthalen-2-yl trifluoromethanesulfonateHCID 86611254—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductN-(6-(isoquinolin-5-yl)naphthalen-2-yl)thiophene-2-carboxamideHCID 11990812100%

Reaction Steps

To a microwave vial containing 6-(thiophene-2-carboxamido)naphthalen-2-yl trifluoromethanesulfonate (0.100 g, 0.2 mmol), in 1,4-Dioxane (3 mL), was added isoquinolin-5-ylboronic acid (0.129 g, 0.8 mmol), Fibrecat catalyst (0.005 g, 5% by wt.), and Potassium Carbonate (2 M, 0.50 mL, 1 mmol). The vial was capped and placed into CEM Microwave for 10 minutes at 80° C., while supplying 50 Watts of power through power-max. The mixture was diluted with DCM (2 mL) and water (2 mL). The aqueous layer was extracted with DCM (3×10 mL). The combined organics was dried over sodium sulfate, filtered, and concentrated in-vacuo. The crude was purified from reverse-phase HPLC. This gave a yellow colored amorphous solid, which was titled product (0.078 g, 0.2 mmol). MS (ESI pos. ion) m/z: 381 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017601B2
Source datasetuspto-grants-2011_09
ORD IDord-6bb87cdc355741958849ce96103e7dcb
Source noteuspto-grants-2011_09