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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403889Generated: October 31, 2026

Iodoethane → HCID 67233766, compound

https://huagongshe.com/reaction/2403889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantAcetonitrileHCID 6342—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Butyloxy)-8-(methyloxy)-9-[3-(2-piperidinyl)propyl]-9H-purin-6-amineHCID 58306184—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67233766HCID 672337666.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A portion of this solution (0.12 ml, equivalent to 0.12 mmol) was added to a test tube. 2-(Butyloxy)-8-(methyloxy)-9-[3-(2-piperidinyl)propyl]-9H-purin-6-amine (435 mg, 1.2 mmol) was dissolved in DMF (6.0 ml) and an aliquot (0.5 ml, 0.1 mmole) dispensed to the tube. DIPEA (40 μL, 0.23 mmol) was added, and heated to 50° C. for 18 hours. An additional aliquot of 1-iodoethane in acetonitrile (80 uL, 0.08 mmol) (total added 0.2 mmol) and DIPEA (40 uL, 0.23 mmol) was added and continued stirring with heat at 50° C. for a further 18 hours. DMSO:MeOH (200 uL) was added, the mixture filtered and purified by Mass Directed AutoPrep (Method A). The solvent was evaporated in vacuo using the Genevac. The residue was redissolved in a solution of 4M HCl/dioxane (0.2 ml) and allowed to stand at room temperature for 4 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 an aminopropyl SPE (0.1 g, 3 ml, preconditioned in methanol (1.5 ml)). The product was eluted with additonal methanol (1.5 ml). The solvent was removed to give the title compound (6 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-a87b9d7224c6421c867cff9231c78f0b
Source noteuspto-grants-2014_08