HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol hydrochloride → 5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | 5'-O-[N-{N-(Nalpha,Nepsilon-di benzyloxycarbonyllysyl)alanyl}isoleucyl]-5-fluorouridine | HCID 67896792 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochloride | HCID 18637340 | 99% |
Reaction Steps
0.94 Gram (1.11 mmol) of the ester obtained as described above was dissolved in ethanol (100 ml) and methanol (20 ml), and 0.40 g of 10% palladium-carbon and 0.50 g (4.93 mmol) of 36% hydrogen chloride-ethanol were added. The mixture was stirred in a stream of hydrogen under normal pressure for 2 hours at room temperature. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was washed with ether (20 ml) to obtain 0.71 g (99%) of the desired 5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochloride as a colorless powdery solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892939 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-a684b95c5bfc41e9adf65dff0b86e3b3 |
| Source note | uspto-grants-1990_01 |