HuagongsheHuagongshe Chemistry Print Report · For research reference only
Alloxan → 5-Hydroxy-5-(2-benzthiazolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Alloxan | HCID 5781 | — |
| Reactant | Benzothiazole | HCID 7222 | — |
| Product | 5-Hydroxy-5-(2-benzthiazolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione | HCID 21271261 | — |
Reaction Steps
By the procedure of Example 38, benzthiazole (2.7 g., 0.02 moles) was converted to its 2-lithio derivative and then reacted with anhydrous alloxan to yield title product, initially isolated as an oil. The latter was crystallized from ether-hexane [2.2 g.; Rf 0.55 (1:1 ethyl acetate:hexane/5% acetic acid)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689336 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-8a9b468035a9458e96d4a4f5d9967faa |
| Source note | uspto-grants-1987_08 |