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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403899Generated: October 31, 2026

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

https://huagongshe.com/reaction/2403899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantIsopropyl iodideHCID 6362—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-butoxy-8-methoxy 9-(piperidin-3-ylmethyl)-9H-purin-6-amineHCID 58306241—
SolventDimethylformamideHCID 6228—
Product6-Amino-2-(butyloxy)-9-{[1-(1-methylethyl)-3-piperidinyl]methyl}-7,9-dihydro-8H-purin-8-oneHCID 6723453830.6%

Reaction Steps

2-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). 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 (11.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-57eeacfea0f44cfeace7341a9338b4dc
Source noteuspto-grants-2014_08