HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Benzoyllamivudine → Lamivudine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Benzoyllamivudine | HCID 10903732 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Lamivudine | HCID 60825 | 90.4% |
Reaction Steps
A suspension of (cis)-4-amino-1-(2-benzoyloxymethyl-1,3-oxathiolan-5-yl)(1H)-pyrimidin-2-one (Intermediate 3) (8.19 g) and Amberlite IRA-400 (OH) resin (8.24 g) in methanol (250 ml) was stirred and heated to reflux for 11/4 h. Solids were removed by filtration then washed with methanol. The combined filtrates were evaporated. The residue was triturated with ethyl acetate (80 ml). The resulting white solid was collected by filtration to give the title product (5.09 g), 1H NMR (DMSO-d6) 3.04 (1H), 3.40 (1H), 3.73 (2H), 5.18 (1H), 5.29 (1H), 5.73 (1H), 6.21 (1H), 7.19 (2H), 7,81 (1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05905082 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-c9cce1c6c73d40baa1fedc1e1bd85be0 |
| Source note | uspto-grants-1999_05 |