HuagongsheHuagongshe Chemistry Print Report · For research reference only
2',3',5'-tri-O-acetyladenosine → N6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2',3',5'-tri-O-acetyladenosine | HCID 96503 | — |
| Reactant | 5-Ethoxy-2-pyrrolidinone | HCID 3580555 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate | HCID 13109688 | 90.8% |
Reaction Steps
Adenosine 2',3',5'-triacetate (2.0 g) and 5-ethoxy-2-pyrrolidinone (1.2 g) were stirred in N,N-dimethylformamide (10 ml) at 130° C. overnight. The reaction mixture was distilled to remove the N,N-dimethylformamide and the residue was subjected to silica gel column chromatography using chloroformacetone (5:3) as the eluent. The active fractions were pooled and concentrated under reduced pressure to give N6 -(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate as an oil (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464361 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-cf2ea343da54445997c69de70ffc7bbe |
| Source note | uspto-grants-1984_08 |