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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366210Generated: October 26, 2026

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

https://huagongshe.com/reaction/1366210

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 numberUS07893058B2
Source datasetuspto-grants-2011_02
ORD IDord-239d6211dad8479b861dabd6ef6bdfe6
Source noteuspto-grants-2011_02