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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017254Generated: October 31, 2026

HCID 136352426, compound → HCID 135804808, compound

https://huagongshe.com/reaction/1017254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136352426HCID 136352426—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
ProductHCID 135804808HCID 135804808100.4%

Reaction Steps

1-(2′,3′,5′-O-Tribenzoyl-β-L-ribofuranosyl)pyrazolo[3,4-d]pyrimidin-4(5H)-one 21 (152 mg, 0.26 mmole) was dissolved in MeOH saturated with NH3 at 0 C (75 mL). The resulting solution stood at room temperature for 24 h and concentrated. The residue was dissolved in water (30 mL), washed with EtOAc (3×15 mL). After evaporation of the water, the crystalline solid was soaked in acetonitrile (2 mL), filtered, and dried under vacuum to give 1-β-L-ribofuranosylpyrazolo[3,4-d]pyrimidin-4(5H)-one 22 as a white crystalline solid (70 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479463B1
Source datasetuspto-grants-2002_11
ORD IDord-37dba053c4d7444bbc4c270a5067823d
Source noteuspto-grants-2002_11