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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223158Generated: October 30, 2026

Acetic Acid → 7-beta-D-Arabinofuranosyl-7H-pyrrolo(2,3-d)pyrimidin-4-amine

https://huagongshe.com/reaction/223158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-MethoxyethanolHCID 3015637—
Reactant7-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 13076215—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product7-beta-D-Arabinofuranosyl-7H-pyrrolo(2,3-d)pyrimidin-4-amineHCID 300791880%

Reaction Steps

A mixture of 2.5 g of 7-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine, 5 ml of acetic acid, 500 mg of 20% of palladium on charcoal, and 95 ml of methoxyethanol is hydrogenated at 50°-55° C. and approximately 3 atmospheres until uptake of hydrogen ceases. The mixture is filtered, evaporated in vacuo, and coevaporated with xylenes to provide a red syrup which is dissolved in water and treated with Amberlite ion exchange resin (20 ml of wet IR-45). The resin is filtered and washed several times with boiling water. The combined filtrates are evaporated in vacuo to provide 992 mg of crude 7-βD-arabinofuranosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine. Recrystallization of this material from water provides 800 mg of product, m.p. 117°-120° C. (after drying at 100° C. for one hour); [α]D25 =+16.2 (1.02% in H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352795
Source datasetuspto-grants-1982_10
ORD IDord-914e99182e304a11983b762119ca3c19
Source noteuspto-grants-1982_10