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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048809Generated: October 30, 2026

Ammonium Chloride → HCID 178507575, compound

https://huagongshe.com/reaction/1048809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178520296HCID 178520296—
CatalystAcetic AcidHCID 176—
CatalystIronHCID 23925—
SolventWaterHCID 962—
SolventWater ethanolHCID 19096565—
ProductHCID 178507575HCID 1785075754.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 152 mg (2.72 mmol) of iron and 70 mg (1.3 mmol) of ammonium chloride in 100 μl of water is added to a solution of 0.24 g (0.544 mmol) of N-(5-(3,5-difluorophenylthio)-1H-pyrazolo[3,4-b]pyridin-3-yl)-2-(4-nitrophenyl)acetamide in 10 ml of a 2:1 ethanol/water mixture. Several drops of acetic acid are added to this mixture and it is heated at 60° C. for 4 hours. After cooling and concentration of the solvents, the crude reaction product is extracted with ethyl acetate and is washed with saturated sodium bicarbonate solution. The organic phases are combined, dried on magnesium sulfate and then concentrated. The crude product is purified by silica gel chromatography (DCM/MeOH) to yield 11 mg (4%) of 2-(4-aminophenyl)-N-(5-(3,5-difluorophenylthio)-1H-pyrazolo[3,4-b]pyridin-3-yl) acetamide in the form of a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09381195B2
Source datasetuspto-grants-2016_07
ORD IDord-ad94bae7a70645f8a0e89bd211dea078
Source noteuspto-grants-2016_07