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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203261Generated: October 29, 2026

Potassium Carbonate → HCID 73438427, compound

https://huagongshe.com/reaction/2203261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridineHCID 24208789—
ReactantHCID 90077584HCID 90077584—
CatalystHCID 178418397HCID 178418397—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 73438427HCID 7343842746.5%

Reaction Steps

9-chloro-1-(3-(trifluoromethyl)phenyl)pyrimidino[5,4-c][1,5]naphthyridine-2,4(1H,3H)-dione (300 mg, 0.77 mmol), 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (188 mg, 0.77 mmol), potassium carbonate (317 mg, 2.3 mmol) and tetrakis(triphenylphosphine)palladium (45 mg, 0.04 mmol) were added to 40 mL dioxane and 2 mL water. The resulting mixture was reacted under reflux in the nitrogen protection for 18 hrs, cooled to room temperature, and concentrated. 40 mL water was added. The resulting mixture was filtered to obtain a crude product, which was dissolved in 10 mL 6N hydrochloric acid, and washed with DCM (4×50 mL). The aqueous phase was added dropwise to an aqueous sodium carbonate solution, filtered, and washed with water. The resulting crude product was washed with methanol to produce 9-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1-(3-(trifluoromethyl)phenyl)pyrimidino[5,4-c][1,5]naphthyridine-2,4(1H, 3H)-dione (170 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365572B2
Source datasetuspto-grants-2016_06
ORD IDord-bc0f73fe9732420c8d3bd460e59e91e7
Source noteuspto-grants-2016_06