Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044960Generated: November 1, 2026

Dimethyl Sulfoxide → 6-Amino-2-(butyloxy)-9-[(1-propyl-3-piperidinyl)methyl]-7,9-dihydro-8H-purin-8-one

https://huagongshe.com/reaction/1044960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-IodopropaneHCID 33643—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-butoxy-8-methoxy 9-(piperidin-3-ylmethyl)-9H-purin-6-amineHCID 58306241—
SolventDimethylformamideHCID 6228—
Product6-Amino-2-(butyloxy)-9-[(1-propyl-3-piperidinyl)methyl]-7,9-dihydro-8H-purin-8-oneHCID 6723355920.7%

Reaction Steps

1-Iodopropane (0.1 mmol) was weighed into a vial and an aliquot (0.3 ml, 0.1 mmol) of a solution of 2-(butyloxy)-8-(methyloxy)-9-(3-piperidinylmethyl)-9H-purin-6-amine (802 mg, 2.398 mmol) suspended in DMF (7.2 ml) was added. DIPEA (40 μl, 0.229 mmol) was added and the tube was capped and shaken to aid dispersion then allowed to stand at room temperature (18 hours). An additional portion of 1-iodopropane (0.05 mmol) was added and the reaction allowed to stand for 18 hours. DMSO (400 uL) was added and the mixture purified by Mass Directed AutoPrep (Method A). The solvent was evaporated in vacuo using the Genevac. The residue was redissolved in 4M HCl/dioxane (0.5 ml), capped and stood at room temperature for 18 hours. The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus. The material was redissolved in methanol (0.5 ml), and applied to a 0.5 g aminopropyl SPE (preconditioned with methanol, 2 CV). The cartridge was eluted with methanol (2 ml), the solvent was removed to give the title compound (7.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563717B2
Source datasetuspto-grants-2013_10
ORD IDord-c9305e972627450eb0d0fe8c41057f33
Source noteuspto-grants-2013_10