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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783967Generated: October 30, 2026

Hydrochloric Acid → 6-(4-Isopropyl-piperazin-1-yl)-pyridin-3-yl-amine

https://huagongshe.com/reaction/1783967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous chloride dihydrateHCID 61436—
Reactant1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazineHCID 33995718—
SolventMethanolHCID 887—
Product6-(4-Isopropyl-piperazin-1-yl)-pyridin-3-yl-amineHCID 4346204286%

Reaction Steps

1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazine (0.9 g, 3.6 mmol) is dissolved in MeOH (20 mL) and tin (II) dichloride dihydrate (4 g, 18 mmol) is added. The mixture is cooled using a water bath and conc. HCl is added (4 mL). The reaction is stirred at room temperature overnight. After removing the methanol, the resultant light yellow solution is basified using conc. NaOH (pH 11) and a white precipitate is formed. The solid is collected by filtration and the water is extracted with diethyl ether (5×). The organic layers are combined, dried over MgSO4, filtered, concentrated under vacuum to afford an orange oil which crystallizes on standing to afford an orange solid (0.68 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-c30382f053ff4f0eb8c94e28cb95ba2f
Source noteuspto-grants-2009_03