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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397987Generated: October 27, 2026

Dimethyl Sulfoxide → (2s,3s,4r,5r)-2-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-5-[6-(1-ethyl-propylamino)-2-(2-pyridin-2-yl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol formate

https://huagongshe.com/reaction/397987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant2-PyridineethanamineHCID 75919—
Reactant(2r,3r,4s,5s)-2-[2-Chloro-6-(1-ethyl-propylamino)-purin-9-yl]-5-(3-ethyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diolHCID 56625647—
Product(2s,3s,4r,5r)-2-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-5-[6-(1-ethyl-propylamino)-2-(2-pyridin-2-yl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol formateHCID 70021404—

Reaction Conditions

Temperature80 °C

Reaction Steps

Intermediate 9 (0.070 g, 0.161 mmol) and 2-(2-aminoethyl) pyridine (0.096 ml, 0.807 mmol) were dissolved in DMSO (0.03 ml) and heated at 80° C. in a sealed vial (eg Reacti vial™), for 46 h, a further portion of 2-(2-aminoethyl) pyridine (0.096 ml, 0.807 mmol) was added after the first 20 h. The product was purified by Autoprep. HPLC to give the title compound after freeze drying as a beige solid (0.035 g). LC/MS system B Rt=2.38 min, m/z=524 MH+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610665B1
Source datasetuspto-grants-2003_08
ORD IDord-470b365d45b34266be29a7f44945f6f9
Source noteuspto-grants-2003_08