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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167411Generated: October 26, 2026

CID 533837 → 2-(2,6-Diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

https://huagongshe.com/reaction/1167411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 533837HCID 533837—
Reactantisopropanol water NH4OHHCID 19893943—
ReactantSilyl trifluoromethanesulfonateHCID 71401765—
ReactantGuanosine HydrateHCID 135705230—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product2-(2,6-Diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diolHCID 222076—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a 2 L stainless steel Parr bomb was added guanosine hydrate (100 g, 0.35 mol, Aldrich), hexamethyl) disilazane (320 mL, 1.52 mol, 4.4 eq.), trimethyl) silyl triflouromethanesulfonate (8.2 mL), and toluene (350 mL). The bomb was sealed and partially submerged in an oil bath (170° C.; internal T 150° C., 150 psi) for 5 days. The bomb was cooled in a dry ice/acetone bath and opened. The contents were transferred with methanol (300 mL) to a flask and the solvent was evaporated under reduced pressure. Aqueous methanol (50%, 1.2 L) was added. The resulting brown suspension was heated to reflux for 5 h. The suspension was concentrated under reduced pressure to one half volume in order to remove most of the methanol. Water (600 mL) was added and the solution was heated to reflux, treated with charcoal (5 g) and hot filtered through Celite. The solution was allowed to cool to 25° C. The resulting precipitate was collected, washed with water (200 mL) and dried at 90° C./0.2 mmHg for 5 h to give a constant weight of 87.4 g (89%) of tan, crystalline solid; mp 247° C. (shrinks), 255° C. (dec, lit. (1) mp 250-252° C.); TLC homogenous (Rf 0.50, isopropanol-ammonium hydroxide-water 16:3:1 ); PMR (DMSO), δ 5.73 (d, 2, 2-NH2), 5.78 (s, 1, H-1), 6.83 (br s, 2, 6-NH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617442B1
Source datasetuspto-grants-2003_09
ORD IDord-dcfc2a3a4b6147a78d4d3dc99aaf4515
Source noteuspto-grants-2003_09