HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Aminothiazolo[4,5-d]pyrimidine-2(3H)-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | 5-Bromopyrimidine-2,4-diamine | HCID 23423590 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Aminothiazolo[4,5-d]pyrimidine-2(3H)-thione | HCID 57756068 | 46.2% |
Reaction Steps
5-Bromo-pyrimidine-2,4-diamine (2.0 g, 10.58 mmol) [prepared in a manner similar to English et. al. J. Am. Chem. Soc. 1946, 68, 453-458] and O-ethylxanthic acid potassium salt (3.39 g, 21.16 mmol) was heated in DMF (25 mL) to 140° C. After 5 h the reaction was cooled to ambient temperature and 25 mL of water was added. The pH was then adjusted to 5.0 using I N HCl. A red precipitate formed and was collected by filtration, yielding 900 mg (30%) of a solid: 1H NMR (400 MHz, d6-DMSO) δ 13.85 (s, 1H), 8.33 (br s, 1H), 6.90 (s 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560544B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-e6c9f81d65dc42f88f86a46cf9686d97 |
| Source note | uspto-grants-2009_07 |