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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092243Generated: October 30, 2026

Ammonium Chloride → (R)-2-(5-amino-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyridin-2-ylamino)-2-(4-fluorophenyl)ethanol

https://huagongshe.com/reaction/1092243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAmmonium AcetateHCID 517165—
Reactant(R)-2-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-nitropyridin-2-ylamino)-2-(4-fluorophenyl)ethanolHCID 66589208—
CatalystZincHCID 23994—
SolventMeOH tetrahydrofuranHCID 21899815—
Product(R)-2-(5-amino-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyridin-2-ylamino)-2-(4-fluorophenyl)ethanolHCID 66589154—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of (R)-2-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-nitropyridin-2-ylamino)-2-(4-fluorophenyl)ethanol (Method 94, 0.14 g, 0.36 mmol) and zinc dust (0.12 g, 1.78 mmol) in MeOH-THF (1:1, 16 ml) was slowly added saturated ammonium chloride (2.0 ml). The reaction mixture was stirred at 25° C. for 1 hour, to which was then added saturated ammonium acetate solution (5 ml). The resulting mixture was stirred for another 30 minutes. The Zn dust was removed by filtration and washed with EtOAc (20 ml). The organic layer was separated, washed with brine (10 ml), dried over sodium sulfate, and concentrated. The crude product was used directly for the next step without further purification. MS: Calcd.: 368; Found: [M+H]+ 369.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129403B2
Source datasetuspto-grants-2012_03
ORD IDord-53c5033a2bc844f589975d1201c0de6f
Source noteuspto-grants-2012_03