HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 4,6-Bis(1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,6-Bis (1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carbonitrile | HCID 15294897 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4,6-Bis(1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carbothioamide | HCID 136093193 | 58% |
Reaction Steps
Hydrogen sulfide is bubbled through a solution of 4,6-bis (1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carbonitrile (4.5 g, 19.3 mmol) and triethylamine (4.3 g, 42.4 mmol) in pyridine (20 nil) at room temperature for 6 hours. The reaction mixture is stirred at room temperature overnight. The solvent is evaporated under vacuum and the residue is recrystallized from ether/hexane to give pure 4,6-bis (1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carbothioamide (3.0 g, 58%); mp 169°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356898 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-3a72580b00e6430a9ac477618631479c |
| Source note | uspto-grants-1994_10 |