HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → Tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Tert-butyl 6-chloropyridine-3-carboxylate | HCID 11521348 | — |
| Product | Tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate | HCID 22142445 | — |
Reaction Steps
The tert-butyl 6-chloropyridine-3-carboxylate was heated with ethylenediamine (20 ml) at 80° C. overnight. The solvent was removed in vacuo. The residue was partitioned between dichloromethane and 2.5 M aqueous sodium hydroxide solution. The aqueous layer was extracted a further three times with dichloromethane. The combined organic layers were washed with water, dried and concentrated in vacuo to give tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06489344B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-d586582582b24fbf967c09c33b057027 |
| Source note | uspto-grants-2002_12 |