HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Diaminopyridine → HCID 13451701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Pyridine tetrahydrofuran | HCID 16069498 | — |
| Product | HCID 13451701 | HCID 13451701 | — |
Reaction Steps
To a solution of 2,3-diaminopyridine in tetrahydrofuran/pyridine (10/1) at 0° C. benzylchloroformate was added dropwise. The suspension was stirred at room temperature and after 2 hours partitioned between water and EtOAc. The organic phase was separated and the aqueous phase was extracted with EtOAc. The combined organic phases were dried over sodium sulfate and the filtrate concentrated to dryness under reduced pressure. To the residue was added Et2O-MeOH and the solid was filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939537B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-4b96f569b809458f94b63f6d610ec9c0 |
| Source note | uspto-grants-2011_05 |