HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → Ammonia
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Chloro-5-ethoxypyridine | HCID 11521128 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 1-(5-Ethoxy-3-pyridyl)piperazine fumaric acid salt | HCID 131724659 | — |
Reaction Steps
A mixture of 3-chloro-5-ethoxypyridine (6.5 g, 45.8 mmol), piperazine (19.7 g, 229 mmol), potassium tert-butoxide (11.2 g, 91.6 mmol) and 1,2-dimethoxyethane (150 ml) was stirred at reflux for 1 h. Aqueous sodium hydroxide (1 M, 100 ml) was added and the mixture was extracted two times with ethyl acetate (150 ml). Chromatography on silica gel with dichloromethane, methanol and conc. ammonia (89:10:1) gave the title compound. Yield 4.6 g, 48%. The corresponding salt was obtained by addition of a diethyl ether and methanol mixture (9:1) saturated with fumaric acid. Mp 160.0-161.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825189B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-d97b429003f4481ea9e62480d0085164 |
| Source note | uspto-grants-2004_11 |