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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397986Generated: 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-piperidin-1-yl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol formate

https://huagongshe.com/reaction/397986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
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-piperidin-1-yl-ethylamino)-purin-9-yl]-tetrahydro-furan-3,4-diol formateHCID 70021909—

Reaction Conditions

Temperature80 °C

Reaction Steps

Intermediate 9 (0.070 g, 0.161 mmol) and 2-piperidinoethylamine (0.115 ml, 0.807 mmol) were dissolved in DMSO (0.03 ml) and heated at 80° C. in a sealed vial (eg Reacti vial™), for 40 h, a further portion of 2-piperidinoethylamine (0.057 ml, 0.403 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 brown gum (0.035 g). LC/MS system B Rt=2.33 min, m/z=530 MH+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610665B1
Source datasetuspto-grants-2003_08
ORD IDord-cb057555c3944caf8ceaf75ccf029e77
Source noteuspto-grants-2003_08