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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Reactant | 7-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 13076215 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-beta-D-Arabinofuranosyl-7H-pyrrolo(2,3-d)pyrimidin-4-amine | HCID 3007918 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04352795 |
|---|
| Source dataset | uspto-grants-1982_10 |
|---|
| ORD ID | ord-914e99182e304a11983b762119ca3c19 |
|---|
| Source note | uspto-grants-1982_10 |
|---|