HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylate → (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylate | HCID 131735158 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate | HCID 131735159 | 92.8% |
Reaction Steps
To a solution of (R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylate (300 mg, 1.019 mmol) in ethanol (15 mL) was added a suspension of 10% palladium-on-carbon (200 mg) in ethanol under nitrogen atmosphere. The mixture was hydrogenated using a hydrogen balloon for 2 h at room temperature then was filtered through a pad of Celite. The filtrate was concentrated to afford (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate (250 mg) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296745B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-2b7ac2ac477e4519be0bc0117ff8f79a |
| Source note | uspto-grants-2016_03 |