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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092238Generated: November 1, 2026

Ammonium Chloride → (S)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N-(1-(4-fluorophenyl)ethyl)pyridine-2,4,5-triamine

https://huagongshe.com/reaction/1092238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAmmonium AcetateHCID 517165—
Reactant(S)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)-5-nitropyridine-2,4-diamineHCID 67478852—
CatalystZincHCID 23994—
SolventMeOH tetrahydrofuranHCID 21899815—
Product(S)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N-(1-(4-fluorophenyl)ethyl)pyridine-2,4,5-triamineHCID 67478872—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of (S)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)-5-nitropyridine-2,4-diamine (Method 89, 0.15 g, 0.40 mmol) and zinc dust (0.13 g, 2.0 mmol) in MeOH-THF (1:1, 16 ml) was slowly added saturated ammonium chloride solution (2 ml). The reaction mixture was stirred at 25° C. for 1 hour, to which was added saturated ammonium acetate solution (5 ml). The resulting mixture was stirred for another 30 min. Zn dust was removed by filtration and washed with EtOAc (20 ml). The organic layer was separated, washed with brine (10 ml), dried over Na2SO4, and concentrated. The crude product was used directly for the next step without further purification. MS: Calcd.: 352; Found: [M+H]+ 353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129403B2
Source datasetuspto-grants-2012_03
ORD IDord-40176cf35b314944b2b25ac010658986
Source noteuspto-grants-2012_03