HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444957Generated: October 25, 2026
Stannous chloride dihydrate → 6-(4-Allylpiperazin-1-yl)pyridin-3-ylamine
https://huagongshe.com/reaction/444957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 1-Allyl-4-(5-nitropyridin-2-yl)piperazine | HCID 69146018 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-(4-Allylpiperazin-1-yl)pyridin-3-ylamine | HCID 69145945 | — |
Reaction Steps
2.2 g (8.86 mmol) of 1-allyl-4-(5-nitropyridin-2-yl)piperazine from Example 1.1 were dissolved in 150 ml of methanol after which 18 g (79.75 mmol) of tin(II) chloride dihydrate were added and the mixture was stirred at 70° C. for 4 hours. After the solvent had been evaporated down to dryness, water was added to the residue. The aqueous reaction mixture was made alkaline with dilute sodium hydroxide solution and then extracted with ethyl acetate. The solid which had precipitated out was filtered off. After that, the phases were separated and the aqueous phase was extracted in each case twice with ethyl acetate and dichloromethane. The combined organic phases were dried over sodium sulfate. 1.74 g (90% of theory) of the title compound were obtained after the drying agent had been removed and the solvent had been evaporated down to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08476275B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-35496fa62dc8472ab85881482fa34b6b |
|---|
| Source note | uspto-grants-2013_07 |
|---|