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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358011Generated: October 31, 2026

N6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetate → N6-(5-oxo-2-pyrrolidinyl)adenosine

https://huagongshe.com/reaction/358011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN6-(5-oxo-2-pyrrolidinyl)adenosine 2',3',5'-triacetateHCID 13109688—
SolventAmmoniaHCID 222—
ProductN6-(5-oxo-2-pyrrolidinyl)adenosineHCID 1314592467.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464361
Source datasetuspto-grants-1984_08
ORD IDord-09ad0f304203499d8bc4681d29466b0d
Source noteuspto-grants-1984_08