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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271260Generated: October 26, 2026

2-Cyclohexylethanol → 9-(2-Cyclohexylethyl)-6-(2-furyl)-9H-purine-2-amine

https://huagongshe.com/reaction/271260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-CyclohexylethanolHCID 20508—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant6-(furan-2-yl)-9H-purin-2-amineHCID 178508247—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product9-(2-Cyclohexylethyl)-6-(2-furyl)-9H-purine-2-amineHCID 5983509858.9%

Reaction Steps

A solution of 6-(2-furyl)-1H-purine-2-amine (25 mg, 0.12 mmol) in anhydrous DMF (0.5 mL) and anhydrous THF (2 mL) was treated with triphenylphosphine polystyrene (65 mg, 0.25 mmol) and 2-cyclohexylethanol (35 mg, 0.25 mmol), shaken at room temperature for 10 min, treated with di-tert-butyl azodicarboxylate (0.058 g, 0.25 mmol), shaken at room temperature for 16 h, filtered and concentrated in vacuo. The resulting oil was dissolved in CH2Cl2 (2 mL) and TFA (1 mL), shaken for 2 h and concentrated in vacuo. The resulting oil was dissolved in CH2Cl2 (3 mL), shaken with 1-M aq HCl (1 mL) for 15 min and the organic phase concentrated in vacuo and purified by chromatography (SiO2; EtOAc) to give the title compound (22 mg, 57%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452894B2
Source datasetuspto-grants-2008_11
ORD IDord-d26ba319f471470d8cfa8588437719c1
Source noteuspto-grants-2008_11