HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-(4-Isopropyl-piperazin-1-yl)-pyridin-3-yl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazine | HCID 33995718 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-(4-Isopropyl-piperazin-1-yl)-pyridin-3-yl-amine | HCID 43462042 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893058B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-239d6211dad8479b861dabd6ef6bdfe6 |
| Source note | uspto-grants-2011_02 |