HuagongsheHuagongshe Chemistry Print Report · For research reference only
N6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate → N6-(5-oxo-2-pyrrolidinyl)adenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate | HCID 13109688 | — |
| Solvent | Ammonia | HCID 222 | — |
| Product | N6-(5-oxo-2-pyrrolidinyl)adenosine | HCID 13145924 | 67.9% |
Reaction Steps
To N6 -(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate (2.2 g) was added cold ammonia-saturated methanol (40 ml), and the resulting mixture was allowed to stand in a refrigerator (at 4° C.) overnight. Next morning the solvent was removed at room temperature. To the residue was added a small amount of methanol and the mixture was allowed to stand at room temperature. The resulting precipitate was recovered by filtration and dried to give N6 -(5-oxo-2-pyrrolidinyl)adenosine as crystals (1.098 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464361 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-09ad0f304203499d8bc4681d29466b0d |
| Source note | uspto-grants-1984_08 |