HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 4-(Piperazin-1-yl)thieno[3,2-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4-Chlorothieno[3,2-c]pyridine | HCID 12827312 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Piperazin-1-yl)thieno[3,2-c]pyridine | HCID 10966027 | 56.1% |
Reaction Steps
A mixture of 4-chlorothieno[3,2-c]pyridine (22.7 g, 0.13 mole) and piperazine (57.7 g, 0.67 mole) were heated in a bomb with a minimum amount of ethanol (50 mL) at 120° for 24 hours. The reaction was cooled, partitioned between dichloromethane and water, and the organic layer was isolated, dried (MgSO4), filtered, and concentrated in vacuo to an oil. Flash chromatography (methylene chloride-10% methanol-1% ammonium hydroxide) of this material gave 16 g (54%) of a golden oil. Treatment of an ethanol solution of the oil with ethanolic HCl followed by recrystallization from ethanol gave the hydrochloride salt as off-white crystals, m.p. 275°-283°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04677104 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-835e7b028b934112bcad12d39be926bf |
| Source note | uspto-grants-1987_06 |