Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017255Generated: October 30, 2026

HCID 136352428, compound → HCID 136352427, compound

https://huagongshe.com/reaction/1017255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136352428HCID 136352428—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
ProductHCID 136352427HCID 13635242795%

Reaction Steps

3-Bromo-1-(2′,3′,5′-O-tribenzoy-β-L-ribofuranosyl)pyrazolo[3,4-d]pyrimidin-4(5H)-one 24 (280 mg, 0.43 mmole) was dissolved in MeOH saturated with NH3 at 0 C (25 mL). The solution in a sealed, stainless steel bomb was heated at 100 C for 6 h. After cooling, ammonia and methanol were evaporated. The residue was dissolved in water (40 mL), washed with EtOAc (4×20 mL), and concentrated. The residue was soaked in acetonitrile and the resulting solid filtered, dried under vacuum to give 3-Bromo-1-β-L-ribofuranosylpyrazolo[3,4-d]pyrimidin-4(5H)-one 25 as a white solid (140 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479463B1
Source datasetuspto-grants-2002_11
ORD IDord-88ce521518df4c329bd7c8b3f0b77dd6
Source noteuspto-grants-2002_11