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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088415Generated: October 31, 2026

Water → HCID 58289757, compound

https://huagongshe.com/reaction/2088415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
ReactantHCID 58289778HCID 58289778—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58289757HCID 58289757—

Reaction Conditions

Temperature80 °C

Reaction Steps

800 mg (1.66 mmol) of 1-[3-(5-bromopyrimidin-2-yl)benzyl]-6-(1-methyl-1H-pyrazol-4-yl)-1H-1,2,3-triazolo[4,5-b]pyrazine is suspended in 10 ml of THF and 1 ml of DMF, and 515 mg (1.99 mmol) of bis(pinacolato)diboron and 488 mg (4.97 mmol) of potassium acetate are added. The reaction mixture is evacuated and flushed with argon a number of times. 16.3 mg (0.023 mmol) of bis(triphenylphosphine)palladium(II) chloride is added, and the mixture is again evacuated and flushed with argon. The reaction mixture is stirred at 80° C. for 24 h. When the reaction of the starting material is complete, 255 mg (1.656 mmol) of sodium perborate trihydrate and 2 ml of water are added to the reaction mixture, which is then stirred at room temperature for 24 h. The reaction mixture is filtered off with suction and washed with ethyl acetate. The filtrate is subsequently adjusted to pH 12 using NaOH solution and extracted with ethyl acetate. The aqueous phase is neutralised using hydrochloric acid and extracted twice with ethyl acetate. The combined organic phases are then dried over sodium sulfate and evaporated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435986B2
Source datasetuspto-grants-2013_05
ORD IDord-fdb9feb4577c4e9ca64de95bb512e7c6
Source noteuspto-grants-2013_05