HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → Ethyl 5-oxo-2-(pyridin-3-yl)pyrazolidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Diethyl Maleate | HCID 5271566 | — |
| Reactant | 3-Hydrazinopyridine | HCID 10909519 | — |
| Reactant | 3-Hydrazinylpyridine dihydrochloride | HCID 17132489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-oxo-2-(pyridin-3-yl)pyrazolidine-3-carboxylate | HCID 118023220 | — |
Reaction Steps
In a preferred reaction, sodium ethoxide in an anhydrous ethanol are introduced into a reaction vessel and 3-hydrazinopyridine.dihydrochloride is added. The mixture is stirred and diethyl maleate is added. The mixture is heated at about 60° C. until most of the 3-hydrazinopyridine has reacted. The mixture is allowed to cool and the excess base is neutralized with acid. The crude ethyl 5-oxo-2-(pyridin-3-yl)pyrazolidine-3-carboxylate (10a) is conveniently isolated and purified by standard techniques.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024031B1 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-973a67849011439b9851380da46bdb5c |
| Source note | uspto-grants-2015_05 |