HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → 2-Thioadenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 5-amino-1-beta-D-ribofuranosylimidazole-4-carboxamide O-cyclohexyl-oxime | HCID 54291096 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Thioadenosine | HCID 6451965 | 65% |
Reaction Steps
0.45 g of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide O-cyclohexyl-oxime was dissolved in a mixture of 0.2 ml of triethylamine and 5 ml of N,N-dimethylformamide, and 0.5 ml of carbon disulfide was further added to the solution. The resulting mixture was allowed to react in an autoclave at 125° C for 5 hours under autogenous pressure (about 10 Kg/cm2) followed by working up in the same manner as described in Example 15 to obtain 0.26 g (yield, 65%) of 2-thioadenosine having a melting point of 197° C (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989682 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-d7de27e4cdc44a67b21a62a41adacfa7 |
| Source note | uspto-grants-1976_11 |