HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium → 2-Thioadenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium | HCID 223 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178507182 | HCID 178507182 | — |
| Product | 2-Thioadenosine | HCID 6451965 | 98% |
Reaction Steps
In the same manner as described in Example 11, 9.6 g of adenosine 1-oxide monohydrate was treated with a 5N sodium hydroxide aqueous solution and Diaion SK-1B (ammonium-type) to obtain a residue. 200 ml of pyridine and then 60 ml of carbon disulfide were added to the above residue, and the resulting mixture was allowed to react in an autoclave at 120° C for 5 hours under autogenous pressure (about 10 Kg/cm2). The reaction mixture was concentrated to dryness, and the residue was worked up in the same manner as described in Example 11 to obtain 9.35 g of 2-thioadenosine as crystals having a melting point of 197° C (with decomposition) in a 98% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989682 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-5bc3059fcc744a9aa5cfd1443b8bbbf4 |
| Source note | uspto-grants-1976_11 |