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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334416Generated: October 30, 2026

Ethyl Acetate → HCID 178509241, compound

https://huagongshe.com/reaction/334416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHydrazinium chlorideHCID 115031—
ReactantHCID 68276347HCID 68276347—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
SolventDichloromethaneHCID 6344—
ProductHCID 178509241HCID 178509241—

Reaction Steps

769 mg (3.12 mmol) of m-chloroperbenzoic acid (mCPBA) is added under argon to a stiring solution of 786 mg (2.83 mmol) of 6-(2,4-difluorophenylamino)-2-(methylthio)nicotinonitrile in 25 mL of dichloromethane. The reaction medium is stirred 1 hour at room temperature before adding a fraction of ethyl acetate and washed this organic phase with a NaHCO3 saturated solution. The combined organic phases are dried on magnesium sulfate and dry evaporated. The crude reaction product is dissolved again in 10 mL of propanol and 2 equivalents of hydrazine hydrochloride in water are 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 495 mg of N6-(2,4-difluorophenyl)-1H-pyrazolo[3,4-b]pyridine-3,6-diamine in the form of a yellow-orange solid (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-e29503f9d2d841c1aa8372286e7f20a9
Source noteuspto-grants-2014_11