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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334417Generated: October 30, 2026

Ethyl Acetate → HCID 178482076, compound

https://huagongshe.com/reaction/334417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHydrazinium chlorideHCID 115031—
ReactantHCID 68276399HCID 68276399—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
SolventDichloromethaneHCID 6344—
ProductHCID 178482076HCID 17848207671.4%

Reaction Steps

452 mg (1.84 mmol) of mCPBA is added under argon to a stirring solution of 486 mg (1.67 mmol) of 6-((2,4-difluorophenyl)(methyl)amino)-2-(methylthio)nicotinonitrile in 15 mL of dichloromethane. The reaction medium is stirred 30 min at room temperature before adding an ethyl acetate fraction. The organic phase is washed with a NaHCO3 saturated solution, dried on magnesium sulfate and dry evaporated. The crude reaction product is dissolved again in 6 mL of propanol and 164 μL (3.38 mmol) of hydrazine hydrochloride in water is added. The mixture is heated at 90° C. for 6 hours before being diluted in water and extracted with ethyl acetate. The organic phase is dried on magnesium sulfate and dry evaporated before being purified by silica gel chromatography to yield 328 mg of N6-(2,4-difluorophenyl)-N6-methyl-1H-pyrazolo[3,4-b]pyridine-3,6-diamine in the form of a yellow-orange solid (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-73d275e6856643aeae058cb2eec22f5b
Source noteuspto-grants-2014_11