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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437442Generated: November 2, 2026

Ammonium Chloride → HCID 68525354, compound

https://huagongshe.com/reaction/1437442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAmmonium AcetateHCID 517165—
Reactant(R)-2-(4-Fluorophenyl)-2-(6-(5-methyl-1H-pyrazol-3-ylamino)-3-nitropyridin-2-ylamino)ethanolHCID 67456085—
CatalystZincHCID 23994—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 68525354HCID 68525354—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of saturated ammonium chloride (3 ml) was added slowly to a suspension of (R)-2-(4-fluorophenyl)-2-(6-(5-methyl-1H-pyrazol-3-ylamino)-3-nitropyridin-2-ylamino)ethanol (Method 63, 0.29 g, 0.78 mmol) and zinc dust (0.25 g, 3.9 mmol) in a mixture of MeOH-THF (1:1, 20 ml). The mixture was stirred at 25° C. for 1 hour. Saturated ammonium acetate solution (5 ml) was added and the mixture was stirred for another 30 minutes. The Zn dust was removed by filtration and the cake was washed with EtOAc (20 ml). The organic layer was separated, washed with brine (10 ml) and dried over sodium sulfate. After removal of solvent, the title compound was obtained which was used directly for the next step without purification. MS: Calcd.: 342. Found: [M+H]+ 343.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622482B2
Source datasetuspto-grants-2009_11
ORD IDord-d737e20daf294b8c8df124e4eae140b9
Source noteuspto-grants-2009_11