HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22819079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Reactant | HCID 53853974 | HCID 53853974 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22819079 | HCID 22819079 | 13.9% |
Reaction Steps
A mixture of 5.9 g of 6-amino-3-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-3,5-dihydro-4H-imidazo-[4,5-c]pyridin-4-one, one g of 20% palladium on carbon, 5 ml of acetic acid, and 95 ml of methoxyethanol is hydrogenated at 50° C. and ca 3 atmospheres until hydrogen uptake ceases, the mixture is filtered, evaporated in vacuo, and co-evaporated with xylenes to provide a syrup which is dissolved in water and treated with 50 ml of wet IR-45 ion exchange resin. The resin is filtered, washed several times with boiling water and the combined filtrates are evaporated in vacuo to provide 2.5 g of crude product. Recrystallization from ethanol-water provides 0.42 g of 6-amino-3-β-D-arabinofuranosyl-3,5-dihydro-4H-imidazo[4,5-c]pyridin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04315000 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-b6e21f13abac4a85b6094c7357dac1d1 |
| Source note | uspto-grants-1982_02 |