Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22065Generated: October 25, 2026

Dextroamphetamine → (R)-2-[(1-Phenylpropyl)amino]adenosine

https://huagongshe.com/reaction/22065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDextroamphetamineHCID 5826—
Reactant(R)-1-PhenylpropylamineHCID 5324978—
Reactant(1S)-1-phenylpropan-1-amineHCID 6993773—
Reactant(S)-2-[(phenylisopropyl)amino]adenosineHCID 67681966—
Product(R)-2-[(1-Phenylpropyl)amino]adenosineHCID 53927112—

Reaction Conditions

Temperature130 °C

Reaction Steps

In Scheme A, step b, the acetonide (2) is then treated with an appropriately substituted primary amine to provide the secondary amine of structure (3). More specifically, the acetonide (2) is combined with a large excess of an appropriately substituted primary amine, such as L-(-)-amphetamine, D-(+)-amphetamine, (R)-1-phenylpropylamine or (S)-1-phenylpropylamine, under an atmosphere of an inert gas such as nitrogen. The mixture is then heated to approximately 130° C. with stirring for approximately 3 to 6 hours. After cooling, the product can be isolated and purified by techniques well known to one skilled in the art. For example, the crude mixture can be directly purified by flash chromatography followed by radial chromatography using an appropriate eluent such as 3% to 6% methanol/chloroform to provide the secondary amine (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426101
Source datasetuspto-grants-1995_06
ORD IDord-91a42dcf5ab743dabf4e25dc19f9830e
Source noteuspto-grants-1995_06